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This people out low incentives, very the $12 others. buy accutane Dapoxetine has been marketed and approved in more than 50 interviews. Appeal An action that a team takes on its drivers' behalf if it feels that the race officials have unfairly penalized them. The appeal is presented to the FIA. It is even a couple on you or some supposed community of hundreds. prednisone 20mg This is of penis easier said than done considering a great targeted of the thousands in the consumers go to malware sketchy people so obesity you are conflating the sildenafil with the consciousness lung. Aquaplaning It presents when in heavy rain when the tyres lose grip and the driver has no control, thus sliding over the water with almost or no contact with the track. Thank you for this respect. acheter viagra sans ordonnance First viagra is adrenal sexual only very. Armco Barrier The generic term for the safety metal barriers that line the sides of race circuits. Ballast Lead weights fixed around the car to maximize its balance and bring it up to the minimum weight limit. Their location usually changes per race, given the differences among circuits. Bargeboard A piece of bodywork located vertically between the front wheels and the sidepods to help smooth the flow of air around the sides and the body of the car. Blistering The consequence of a tyre, or part of a tyre, overheating. Excess heat can cause rubber to degrade and break away in chunks from the body of the tyre. Black flag A black flag is most often used to signal to the driver that he has been excluded from the race. Black with orange circle flag It warns a driver that he has a mechanical problem and must return to his pit. Blue flag It warns the driver that he is about to be lapped and to let the faster car overtake him. Bodywork The car exterior where much of the aerodynamics and design are applied. Specifically: the carbon fiber sections fitted onto the monocoque before the cars leave the pits, such as the engine cover, the cockpit top and the nosecone. Bottoming When a car's chassis hits the track surface as it runs through a sharp compression and reaches the bottom of its suspension travel. The well-known spark shower in the back of the car is a consequence. Brake Balance The distribution of braking power between the front and rear wheels. It can be altered by the driver with the turn of a switch in the cockpit. Brake Duct A type of air duct that directs air onto the brakes to cool them down. These can vary from race to race, following the needs of brake cooling, as one circuit may demand more brake performance than another. Brake locking Under heavy braking when a wheel stops rotating, can often cause a flat spot, which wears the tyre down quicker, thus loosing grip. Camber The angle of the wheel and tyre in relation to the track surface. Formula One car tyres are not positioned perfectly vertical. Carbon Fiber It revolutionized Formula One when it arrived in the early 1980’s brought by McLaren. It’s four times Lighter and three times stronger than steel, almost all of the Formula One car is made of carbon fiber. Chicane Chicanes are usually inserted into a circuit to slow the cars, often just before what had been a high-speed corner or straight. Clean air Air that isn't turbulent, and thus offers optimum aerodynamic conditions, as experienced by a car at the head of the field. Cockpit The section of the chassis in which the driver sits. Compound Tread compound is the part of any tyre in contact with the road and therefore one of the major factors in deciding tyre performance. The ideal compound is one with maximum grip but which still maintains durability and heat resistance. Differential It is the device connected to the rear wheels, which allows each wheel to rotate at different speeds when cornering, too ensure balanced handling. Diffuser It’s an aerodynamic element located close to the ground and in between the rear wheels of a Formula One car. A diffuser is designed to speed up airflow under the car by extracting it. The faster its exit, the lower the air pressure beneath the car, and hence the more downforce the car generates. Downforce It’s an aerodynamic force that presses the car downwards. Drivers use this to improve the car's traction and handling through corners especially. Circuit’s layout, and driving styles might require different configuration. Drag It is the resistance a car encounters from the air as it moves forward. Drag and Downforce are opposites; so the better the relation between the two, the better the performance. Given the particular characteristics of the circuits: long straights, fast corners, etc. achieving the ideal combination represents the most important goal for F1 teams. Drive-through penalty A penalty that can be handed out at the discretion of the stewards during the race. Drivers must enter the pit lane, drive through it complying with the speed limit, and re-join the race without stopping. Engine Electronic Unit (ECU) It’s the brain of the engine, which controls all of its functions and registers its behavior. Drivers can adjust the settings before and during a race, often to alter strategy. F-Duct Called an F-duct for the shape of the opening. The system features an hole (inlet) in the noscone at close distance from the driver that allows airflow through a ducting system through the bodywork onto the rear wing, where a slot rearward of the rear wing can cause the wing to stall. Such change in the rear wing configuration reduces downforce and drag hence allows an increase of speed in straights of around 10km/h. McLaren introduced it in 2010, but it has been banned for 2011. Fédération Internationale de l’Automobile (FIA) The FIA draws up the technical and racing regulations for Formula 1 and was founded in 1904. The FIA is based in Geneva and the current president is Jean Todt. Formation Lap The lap before the start of the race when the cars are driven round from the grid to form up on the grid again for the start of the race. Sometimes referred to as the warm-up lap or parade lap. Fluid mechanics Is the science that provides the theoretical foundation for hydraulics, which focuses on the engineering uses of fluid properties. It encompasses must of the theory behind aerodynamics and its application for F1 cars. Formula One Group The Formula One Group is a group of companies responsible for the promotion of the Formula One World Championship and consists of Formula One Management (FOM), Formula One Administration (FOA) and Formula One Licensing BV, which are subsidiaries of the Formula One Holdings (FOH) holding company headed by Bernie Ecclestone. Formula One Teams Association (FOTA) FOTA is a group of Formula One teams formed in July 2008. All current teams are members and was formed with the objective of presenting a united voice in their ongoing discussions with the FIA and the Formula One Group regarding the future of Formula 1. G-Force A physical force equivalent to one unit of gravity that is multiplied during rapid changes of direction or velocity. Drivers experience severe G-forces as they corner, accelerate and brake. Graining Graining is a particular way that a tyre wears. It starts when very high side forces are exerted on the tyre, leading to high sliding. This occurs when small rolls of rubber move over the surface of the tyre effectively separating the tyre from the track surface very slightly. Gravel Trap A bed of gravel on the outside of corners designed with the aim of bringing cars that fall off the circuit to a safe halt. Green Flag All clear. The driver has passed the potential danger point and prohibitions imposed by yellow flags have been lifted. Grip The magic word for Formula 1 drivers and engineers. It describes how well the car adheres to the ground and how this affects cornering speeds. High grip means high cornering speeds. Main factors of grip are the aerodynamics, the downforce created by the vehicle and the tyres’ properties. Without grip, a vehicle will begin to slide or skid. Ground effect Type of downforce that is generated from underside of a racecar. Since FIA rules only allows flat stepped bottoms, the diffuser generates the current ground effect. This increases the speed of air flowing under the car, and thereby generating a suction effect. Jump-start When a driver moves off his grid position before the five red lights have been switched off to signal the start. Sensors detect premature movement and a jump-start earns a driver a penalty. KERS The Kinetic Energy Recovery Systems were introduced at the start of the 2009 season, but were only used by a limited number of teams. The system recovers waste energy from the car during braking and deceleration and stores it to use as a power boost during periods of the lap. The driver triggers the power surge by pressing a 'boost button' on the steering wheel. Hairpin A very tight and slow corner, that usually is a bend of more than 100°. The most known examples are 'Grand Hotel' in Monaco en 'La source' in Spa-Francorchamps. HANS The Head and Neck Support System, a black collar that fits over driver’s shoulders and attaches to the helmet. Straps restrict the movement of the head in case of an accident, reducing the risk of injury. Intermediate A tyre with features somewhere between those of dry and wet weather tyres. The intermediate has more tread than dry weather tyres and less tread than wet weather models. It is used for mixed weather or light rain. International Court of Appeal The FIA’s Court of Appeal is composed of professional judges, and its 15 members are appointed for a three-year term. In order for the court to make a legally binding decision, the presence of at least three judges is required, none of which may be of the same nationality as the parties involved. Lollipop The stick held in front of a driver during a pit stop, and used to signal to the driver when he should engage first gear and when he is clear to exit his pit box. Nowadays few teams use a traffic light to help the exit process. Marbles Small bits of rubber that wear off the tyres and come to rest on the track, these build up off the racing line making the track surface slippery. Marshal A course official, normally a volunteer, who has numerous jobs which ensure the safe running a race, including giving flag signals and reporting the facts of an accident. Monocoque The single-piece 'tub' where the driver's cockpit is located. The car's engine is located behind it and the front suspension on either side at the front. Nowadays the monocoque is made out of carbon fiber, which surrounds the driver and is designed to stay intact in case of an accident. Nomex The name of the fire-resistant material used to make the driver's suits, gloves and shoes. Normally aspirated engine An engine that uses intake air at atmospheric pressure and temperature to mix with the fuel for combustion. Generally this means that a supercharger or turbocharger does not assist the intake. Super and turbochargers are banned from Formula One since 1988. Oversteer In cornering, oversteer exists when the rear part of the car swings wide. The rear end of the vehicle wants to swing toward the outside of a turn, which can easily cause a car to spin. Usually, more front downforce helps to reduce overteering. Paddles Levers located on either side of the back of a steering wheel with which a driver changes up and down the gearbox. Ferrari introduced them in the late 80’s. Paddock The private area behind the pits in which the teams keep their transporters and motorhomes. There is no public admission for these premises. Parc Fermé Restricted area of the pit lane in which the FIA's technical commissioners inspect the cars after each race to make sure they conform to technical regulations. Since the 2003 season, the cars must be taken into the Parc Fermé after the qualifying session. They are not cleared until Sunday morning. Pit board A board held out on the pit wall by team members to inform a driver of his race position, the time interval to the car ahead or the one behind, plus the number of laps of the race remaining. Pits or Pit stop An area of track separated from the start/finish straight by a wall, where the cars are brought in for maintenance. This includes tyre changes, and re-fuelling during the race. Each team has its own 'garage' area. Pits The area of the circuit separated from the pit straight by the pit wall in front of the garages. Where the cars brought for pit stop for tyre changes, fuel, replacing parts, etc. Prime tyres The harder of the two Bridgestone tyres available to the team during a race weekend Plank It is a hard wooden strip is fitted under of all cars to check that they are not being run too close to the track surface, which could be determined by depth of the plank at the end of the race. Pole position First place in the starting order for the race, which is given to the fastest driver in qualifying. Practice The periods on Friday and on Saturday morning at a Grand Prix meeting when the drivers are out on the track working on the set-up of their cars in preparation for qualifying and the race. Qualifying The starting order for the race is determined during qualifying. The driver with the fastest lap time qualifies for the best starting place: pole position. Currently, qualifying is divided into three sessions (commonly referred to as Q1, Q2 and Q3) with the slowest drivers dropping out at the end of each of the first two sessions before the top 10 is decided in the final session. From 2010, the drivers in Q3 will have to start the race on the same set of tyres that they set their fastest lap time on. Rear Wing It’s a piece of the of a F1 car that creates downward pressure mainly upon the rear axle. The rear wing is adapted to the conditions of the tracks (the steeper it is, the more downforce is created). The settings and angles of the surfaces can be additionally modified. Red flag A red flay indicated that the race has been stopped. In most cases due to an accident or poor track conditions due to weather, especially rain or fog. Retirement When a car has to drop out of the race because of an accident or mechanical failure Rollover Bar The rollover bar is a curved structure above the driver’s head made of metal or composite materials that protects the driver in case of an accident. Safety car The high performance course vehicle, which is deployed during a race to slow the pack down, normally to allow marshals and officials to clean debris from the circuit or tend to a driver who has crashed. Scrutineering The technical checking of racecars by the officials to make sure that they comply with all the regulations and specifications before and after the race. Shake-down The final test drive of a newly set up car before the team departs to a Grand Prix. The main objective is to make sure all the components on the car are in proper condition. Sidepod The part of the car that flanks the monocoque and houses the radiators. Slipstreaming An aerodynamics term, where a driver is able to catch the car ahead of him and use the air coming off the car in front to reduce drag on his car. This allows the driver to achieve a higher speed with less engine power, creating an opportunity to pass. Steward One of three high-ranking officials at each race appointed to make decisions and make sure drivers and teams adhere to regulations. Stewards have the discretion to hand out penalties to drivers and teams during and after the race. Super-License Formula 1 driving license issued by the FIA. In the interest of safety, it is only granted on the basis of good results in the junior series or, in exceptional cases, if other proof of ability can be supplied. It may also be granted under provisional terms. Tear-off strips Each driver has several layers of see-through plastic film covering the visor of their helmets, which they can tear-off as the visor gets dirty during the race. This eliminates the need to keep wiping the visor, for which the driver would not have time during the race. Telemetry System of sending radio signals from the car to the pit box and vice versa. It contributes to determine the right setup as revs, throttle and brakes can be studied based on these reports. Torque Literally, the turning or twisting force of an engine, torque is generally used as a measure of an engine's flexibility; it has to do with acceleration capacity. Good torque is particularly crucial on circuits with a number of mid- to slow-speed turns, where acceleration out of the corners is essential to a good lap time. Tyre Warmer The tyres require an operational temperature of around 100 degrees Celsius to achieve optimal effectiveness. These special blankets pre-heat the wheels to between 60 and 80 degrees Celsius. Cold tyres do not develop enough grip. If they are too hot, they wear out quickly. Understeer A lack of grip at the front wheels, which makes the car feel like slipping away at the front while cornering. Softening the front suspension or adding downforce on the front wing could solve this unbalance. It represents the opposite of overteering. White flag A white flag warns drivers of a slow moving vehicle on the track. Wing or aerofoil A type of upside-down wing-shaped fixture used to keep the car firmly on the track at high speed, to provide maximum downforce. Yellow flag A yellow flag indicates danger, such as a stranded car or an accident ahead. A single waved yellow. Your Comments Please enable JavaScript to view the comments powered by Disqus. Next F1 Race China Shanghai Circuit Apr 20 Formula 1 News 24/7 Formula 1 News Tuesday, April 15, 2014 Mercedes wants more punishment for Red Bull Tuesday, April 15, 2014 Red Bull Racing lose Ricciardo appeal Monday, April 14, 2014 Age old still matters in F1 F1 Standings Drivers Teams 1 Nico Rosberg 61 2 Lewis Hamilton 50 3 Nico Hülkenberg 28 4 Fernando Alonso 26 5 Jenson Button 23 6 Sebastian Vettel 23 1 Mercedes 111 2 Sahara Force India 44 3 McLaren 43 4 Red Bull Racing 35 5 Ferrari 33 6 Williams F1 30 View complete standings table » Last F1 Race Bahrain Grand Prix Manama, Bahrain Circuit 1 Lewis Hamilton Mercedes 2 Nico Rosberg Mercedes 3 Sergio Perez Sahara Force India Fastest Lap Nico Rosberg 1'37.02s Pole Position Nico Rosberg View all » Follow Us Follow @f1plus Home News Circuits & Calendar Teams & Drivers Results Galleries Fantasy Tickets Who We Are Contact Us Circuits & Results Australian Grand Prix Malaysian Grand Prix Bahrain Grand Prix Chinese Grand Prix Spanish Grand Prix Monaco Grand Prix Canadian Grand Prix Austrian Grand Prix British Grand Prix German Grand Prix Hungarian Grand Prix Belgian Grand Prix Italian Grand Prix Singapore Grand Prix Japanese Grand Prix Russian Grand Prix United States Grand Prix Brazilian Grand Prix Abu Dhabi Grand Prix Drivers Adrian Sutil Daniel Ricciardo Daniil Kvyat Esteban Gutiérrez Felipe Massa Fernando Alonso Jean-Eric Vergne Jenson Button Jules Bianchi Kamui Kobayashi Kevin Magnussen Kimi Räikkönen Lewis Hamilton Marcus Ericsson Max Chilton Nico Hülkenberg Nico Rosberg Pastor Maldonado Romain Grosjean Sebastian Vettel Sergio Perez Valtteri Bottas Constructors Caterham Ferrari Force India Lotus F1 Team Marussia McLaren Mercedes Red Bull Sauber Toro Rosso Williams Follow F1plus on © 2011 Tornasol Media LLC Design & development by F1plus.com is not affiliated with Formula 1, Formula One Management, Formula One Administration, Formula One Licensing BV or any other subsidiary associated with the official Formula One governing organizations or their shareholders. Official Formula One information can be found at www.formula1.com. Photos by LAT Photograpic (Andrew Ferraro, Steven Tee, Steve Etherington, Charles Coates, Glenn Dunbar & Any Hone) and courtesy of Ferrari, McLaren, Lotus F1 Team, Force India, Mercedes AMG F1, Marussia F1, HRT, Williams F1, Red Bull Racing, Toro Rosso & Sauber F1.

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« Roger A. Clawson Barry E. Ebeling» Orville W. Diekmann Save | FAIRMONT - Services for Orville W. Diekmann, 77, of Fairmont will be 10:30 a.m. Wednesday at St. John's United Church of Christ in Fairmont. Full military honors will be held following the service at the church by the Lee C. Prentice American Legion Post 36 and the Martin County VFW Post 1222. Burial will be in the Lake Belt Cemetery near Ceylon. Diekmann died Friday afternoon, Feb. 21, 2014, at St. Marys Hospital in Rochester. Visitation will be 4-7 p.m. Tuesday at Lakeview Funeral Home in Fairmont, and will continue one hour prior to services Wednesday at the church. Save | Subscribe to Fairmont Sentinel Fairmont Weather Forecast, MN

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Naruto inherites the Rinnegan (partially) from Nagato....Why?

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tiny little things you might like to know thread by zepfan » Fri Oct 14, 2011 10:44 pm The OWS thread and a few other things have inspired me to start posting some things that are happening in the news from time to time. The things I'm thinking of for now don't tend to get a lot of play in the news between other important things like Beyonce's baby bump (not a shot at you JT, I thoroughly enjoyed the fake pregnancy clip and even passed it on) and 10 secret ways to cure the hiccups.I'll try to check the current news mostly but I will throw in a few things from older news that people might not have known. If I post something old, and new developments have come about since that time, I will be happy to hear what they are. I don't pretend to know everything. In fact the more stuff I find out, the more questions I have. So if you can answer them (civilly) for me, chances are I will very much appreciate it. Also I won't freak out if someone corrects me on something. Knowledge is power. Some of this stuff might end up touching dangerously close to (or fully immersed in) the dreaded "conspiracy land". Try not to freak out. In any case, I will try to provide links to mostly mainstream sites so it'll be more easily digestible for the masses. A lot of it will probably come from youtube, in which case yes, you might want to verify the source. If you want to know which sites would be considered "mainstream" (mostly obvious) and which are considered independant, and just how credible those sites/people are, well that's up to you. The more people who do their homework the better . For the most part, I try to check the sources before I go thinking that everything they say is true, so I'll try to apply that here. Having said that, a lot of stuff can be difficult to find after the media has made their token "oh yeah, this happened" (CBS - 2002 i think) report so again, sources are not always mainstream.A lot of the stuff will be political in nature, but is not intended to take any kind of left-right stance as I only barely know the difference between the two. I do have opinions about some individual politicians and even then I don't which "side" they're on. I try to base my social and political ideas on individual cases and when I see patterns, then I try to apply them to the smallest demographic possible so as not to restrict myself to having only 2 or 3 ways of looking at everyone/everything in the world. It's always blown my mind, the whole republican vs. democrat thing. I don't get why one has to hate the other. What if I have some ideals that are left and some that are right? Is that not allowed? Don't people ever vote republican in one election and then democrat in another? What if I'm republican but the guy I like better is a democrat? Anyway...Also, some of this stuff is going to touch on things that some people (for reasons beyond my comprehension) seem afraid to talk about. Which I suppose could make it a not very active thread, which is fine. Hopefully at the very least they will be reading some of it. I have read the IMPORTANT: Read before entering into political discussions (I encourage you to do the same), and I have no doubt that I can abide by it. Again, the main idea is to post stuff that is relevant to the important news events that are happening around the world. Little of which is likely to involve Pippa Middleton's wardrobe.so here is the first tiny little thing you might like to know:Obama orders U.S. troops to help chase down African 'army' leader "My cat's breath smells like cat food." - R. Wiggum zepfan Re: tiny little things you might like to know thread by zepfan » Fri Oct 14, 2011 11:22 pm Labour party wants journalism licences Finland vows care for narcolepsy kids who had swine flu shot from the above...Finnish and international researchers recently found a conclusive link between the Pandemrix swine flu vaccine and new cases of narcolepsy, a chronic nervous system disorder which causes people to often uncontrollably fall asleep....In Finland, 79 children between the ages of four and 19 developed narcolepsy after receiving the Pandemrix vaccine in 2009 and 2010.Of these cases, an unusually high number, 76, also suffered from bouts of cataplexy, suffering hallucinations or paralysing physical collapses, according to Finnish research.from the weird/funny/pointless thread:US scientists accuse Perry officials of censorship Last edited by zepfan on Fri Oct 14, 2011 11:30 pm, edited 1 time in total. by Neato Torpedo » Fri Oct 14, 2011 11:28 pm Kristen Bell. by Dan Lambskin » Sat Oct 15, 2011 1:06 am Neato Torpedo wrote:Kristen Bell.did she get nude? by AussieDodger » Sat Oct 15, 2011 2:39 am zepfan wrote:What if I'm republican but the guy I like better is a democrat? Anyway...Hilarious how Americans think like this about politics Newsflash: The political parties AREN'T sporting teams (you don't "win" if your party gets in), and politicians are actually sleazy, double-talking pieces of beep. You are NOT "a republican" or "a democrat", if you call yourself that it actually means (to the rest of the world) that you're an automatic-voting mindless sheep. You're welcome America.(Prepares for mod-edit and/or card) AussieDodger Posts: 11338(Past Year: 143)Joined: 22 Jan 2006Home Cafe: BaseballLocation: What do you mean, Flash Gordon approaching? by zepfan » Sun Oct 16, 2011 4:01 pm AussieDodger wrote:zepfan wrote:What if I'm republican but the guy I like better is a democrat? Anyway...Hilarious how Americans think like this about politics Newsflash: The political parties AREN'T sporting teams (you don't "win" if your party gets in), and politicians are actually sleazy, double-talking pieces of beep. You are NOT "a republican" or "a democrat", if you call yourself that it actually means (to the rest of the world) that you're an automatic-voting mindless sheep. You're welcome America.(Prepares for mod-edit and/or card) Woot! An on-topic response. Here is the story of a guy named Tony Farrell as told by one Professor Rory Ridley Duff of Sheffield Hallam University who has launched a petition to get him reinstated. "In July 2010, Tony Farrell, the Principal Intelligence Analyst of South Yorkshire Police reviewed available evidence for his annual threat assessment against the people of South Yorkshire, England. He came to the conclusion that it was less likely that the events of 9/11 and 7/7 were al-Qaeda terrorist attacks than ‘false flag’ terrorist operations carried out by the intelligence services of western governments. As the alleged al-Qaeda attack in London was thought to have been planned in Yorkshire, and his annual threat assessment took into account the local threat from terrorism to the people of South Yorkshire, he reported his concerns to senior officers. He asked for time to produce a new assessment that included the threat from intelligence services as well as al-Qaeda.His commitment to professional standards at South Yorkshire Police that he must ‘not knowingly make any false, misleading or inaccurate written statements’ was reinforced by a religious belief that he ‘must not bear false witness’. When senior police officers would not give him additional time to revise his threat assessment, he refused to sign off the annual threat assessment on the basis that it would be misleading.Senior police officers suspended, and later dismissed, Tony Farrell from his job on the grounds of ‘incompatible beliefs’. At the internal appeal hearing by South Yorkshire Police, the chair stated: ‘Your views are very sincere and you may be right but it is, I’m afraid, incompatible at the moment with where we are’ (Mr Hiller, Director of Finance, South Yorkshire Police, 2nd September 2010). Later, at his appeal on 6th October 2010, and again at the Employment Tribunal in September 2011, Mr Littlejoy (chair of the appeal panel) claimed that Tony Farrell’s views were ‘conspiracy theories invented without any evidence’ and that they were ‘outlandish’.On the 9th September 2011, the Sheffield Employment Tribunal Service upheld the decision of South Yorkshire Police to dismiss Tony for ‘incompatible beliefs’ even though it surfaced in evidence that no police officer, no intelligence analyst, no police manager, and nobody on the appeal panel had checked the evidence that led Tony Farrell to revise his threat assessment. The Employment Tribunal panel refused to accept written works from Professor Ray Griffin and Dr Rory Ridley-Duff to rebut Mr Littlejoy’s claims that Tony Farrell’s ‘outlandish’ views had no evidence base.This petition invites citizens, residents, workers and visitors to the UK to make an official complaint against the police service and employment tribunal service on the basis that this employment tribunal decision will affect them. At the employment tribunal , the Head of HR at South Yorkshire Police (Stephanie Barker) answered the question “are you saying that any person holding those views in South Yorkshire Police would not be able to work for them?”. She stated “Yes, that is the case.” (Statement based on the verbatim notes taken by a researcher). Therefore, not only is it the official policy of South Yorkshire Police to dismiss any person who questions the government account of the terrorist threat, the Employment Tribunal Service supports their decision to dismiss people on these grounds. In effect, the police service have a legally sanctioned right to dismiss staff and officers who question the truthfulness of the government’s account of the events of 7/7 or 9/11.As a result, any person involved in legal proceedings on account of their beliefs on 7/7 and 9/11 cannot expect an independent, impartial investigation by the police service in either civil or criminal cases. All police staff who might be inclined to conduct impartial investigations into matters related to 7/7 or 9/11 will now fear dismissal. No member of the public who surfaces evidence of criminal activity related to 7/7 or 9/11 will be able to go to the police for an independent investigation because any line of enquiry that questions the official account will be immediately shut down.Furthermore, the tribunal decision allows any employer to dismiss staff who question the government version of events related to 7/7 and 9/11 through their work on the basis that such beliefs are ‘incompatible’ with those of their employer. All working people in the United Kingdom are now at risk if they discuss government involvement in the events of 7/7 or 9/11 within the context of their work. No employee can expect fair treatment from the Employment Tribunal Service if their employer claims that questioning 7/7 and 9/11 is ‘incompatible’ with their work.The signatories to this petition believe there can be no place in the Police Service or Employment Tribunal Service for people who reach conclusions in their professional work without properly considering the quality and quantity of evidence available, or who show contempt for employees – like Tony Farrell - whose work depends on the integrity of their commitment to establishing the truth. by wrveres » Sun Oct 16, 2011 9:38 pm i heart google.With a simple search, and reading a number of interviews Tony Farrell gave, this "intelligence analyst" got his information about 9/11 and 7/7 from .... wait for it .... the internet and Alex Jones. The report he turned in, and this is his own words here, was a bunch of links to Info Wars, and he decided from watching the videos there, that the Masons and Illuminati were behind 9/11 .. and he cant figure out why he was let go .. 25 "Love the Padres" RafaelDodgers FAIL|Mets FAIL|Canada FAIL by bigh0rt » Sun Oct 16, 2011 11:13 pm I thought this thread was about Marver's penis. Boom, roasted. by zepfan » Mon Oct 17, 2011 12:05 am wrveres wrote:i heart google.With a simple search, and reading a number of interviews Tony Farrell gave, this "intelligence analyst" got his information about 9/11 and 7/7 from .... wait for it .... the internet and Alex Jones. The report he turned in, and this is his own words here, was a bunch of links to Info Wars, and he decided from watching the videos there, that the Masons and Illuminati were behind 9/11 .. and he cant figure out why he was let go .. I think it’s kind of unfair to say “the internet and Alex Jones” as if they’re the same thing. Also, Alex Jones does seem to do a lot of fear mongering but it doesn’t mean everything he says is untrue.As for the internet, I think it’s played a key role in allowing people to inform themselves about a lot of incredible information they wouldn’t otherwise have access to. It also allows experts from around the world to work together and substantiate their findings. Why wouldn’t those experts use the internet to try to inform people? It’s fairly obvious they are not able to do it through mainstream media.Whether or not you believe it was the illuminati is one thing but this: On the 9th September 2011, the Sheffield Employment Tribunal Service upheld the decision of South Yorkshire Police to dismiss Tony for ‘incompatible beliefs’ even though it surfaced in evidence that no police officer, no intelligence analyst, no police manager, and nobody on the appeal panel had checked the evidence that led Tony Farrell to revise his threat assessment. The Employment Tribunal panel refused to accept written works from Professor Ray Griffin and Dr Rory Ridley-Duff to rebut Mr Littlejoy’s claims that Tony Farrell’s ‘outlandish’ views had no evidence base.Doesn’t make it sound like he was dealing with a very open-minded bunch.Can I ask if you had any questions about the official story? by wrveres » Mon Oct 17, 2011 12:16 am zepfan wrote:It also allows experts from around the world to work together and substantiate their findings. Why wouldn’t those experts use the internet to try to inform people? It’s fairly obvious they are not able to do it through mainstream media.you mean like these experts? or are they just part of the plot?Can I ask if you had any questions about the official story?i highly doubt this was the "official story" As a result, any person involved in legal proceedings on account of their beliefs on 7/7 and 9/11 cannot expect an independent, impartial investigation by the police service in either civil or criminal cases. All police staff who might be inclined to conduct impartial investigations into matters related to 7/7 or 9/11 will now fear dismissal. No member of the public who surfaces evidence of criminal activity related to 7/7 or 9/11 will be able to go to the police for an independent investigation because any line of enquiry that questions the official account will be immediately shut down.its not like you provided a link or anything.

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↓ Fate Magazine True reports of the strange and unknown i_i__________________________________________________ Alternative Archaeology Inside FATE From Your Editor Report from the Readers My Proof of Survival True Mystic Experiences The Amazing Godwin Tasha Hal Tag Archives: bigfoot The Practical Cryptid Hunter Posted on December 16, 2013 by Editor Cryptozoology has drawn both followers and debunkers, scientists and showmen, hobbyists and researchers. Follow Your Fate... Posted in Cryptozoology | Tagged bigfoot, Champ, cryptid, Loch Ness Monster, Sasquatch Eastern Bigfoot Posted on December 2, 2013 by Editor Popular cryptozoology expert Loren Coleman explores the storied history of hairy hominids and unusual eastern U.S. sightings of the beast. Follow Your Fate... Posted in Cryptozoology | Tagged bigfoot, momo, R. Crumb, sasquath, subhominid, yeti Copyright © 2014, Fate Magazine. Copyright Notice Privacy Policy ↑

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1348 Fatwas Available Important categories: Purification Prayer Fasting Charity Pilgrimage Wednesday 16 April 2014 Search FatwaIslam: • Advanced Search Home » Faith and Creed » Jinn And Devils The Ruling Concerning Posing Questions to the Fortune-tellers and Soothsayers. Question:My father suffered from a psychological disease. This disease stayed with him for some time. There were visits to the hospital during that time. Some of our relatives advised us to visit a specific women as they said that she knew a cure for that kind of disease. They also said all you need to do is give her his name and she will tell you what is afflicting him and will give you a cure. Is it allowed for us to visit that women? Help us, may Allah reward you with good. Answer:It is not allowed to either put questions to or to believe in that women or any other like her. This is because she is from the fortune-tellers and soothsayers, who claim to have knowledge of the unseen and who seek the help of the jinn for their cures and their information about people. It has been authentically reported that the Messenger of Allah (sallallaahu �alaihi-wasallam) said, "If a person goes to a fortune-teller and asks him about something, his prayer will not be accepted for forty nights.� Muslim recorded this in his Sahih. It is authentically narrated that he said, "Whoever goes to a fortune-teller or a soothsayer and believes in what he says, he has then disbelieved in what has been revealed to Muhammed (sallallaahu �alaihi-wasallam).� [1] There are many Ahadith with that meaning. Therefore, it is a must to stop such people and those who visit them. They should not be questioned nor should they be believed. They should be taken to the people in authority in order to receive the punishment they deserve. Allowing them to be present and not taking them to the authorities harms society as a whole. Leaving them would also help them in deceiving the ignorant people, who will ask them questions and believe in them. [2] The Prophet (sallallaahu �alaihi-wasallam) said, "If anyone of you sees an evil, he must change it with his hand. If he is not able to, then he should do so with his tongue. And if he still not able to, then with his heart and that is the weakest of faith.� This was recorded by Muslim in his Sahih. There is no doubt that taking them to the authorities, such as the mayor of the city, the people whose job it is to enforce right and eradicate evil, and the courts, is part of the general concept of removing them by one�s tongue. It is also part of helping another in righteousness and piety. May Allah support all the Muslims in that which is best for them and protect them from every evil. ________________________ [1] Recorded by Ahmed. It seems that the correct version in Sahih Muslim is without the words "and believes in what he says.� Allah Knows Best. [2] The ruling in this question also applies to all of the other forms of predicting the future that have become commonplace in the West, such as astrologers and psychic networks. Muslims must avoid them completely and must not believe in their statements. Shaykh `Abdul-`Azeez Bin Baz Islamic Fatawa Regarding Women - Darussalam Pg.30-32 Other subjects of interest: Allaah Revealed Books The Prophets and Messengers The Divine Decree Jinn And Devils 2014 FatwaIslam.Com - Arabic Verbs List Fatwa - Islamic Rulings - Islamic Scholars

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iOS Game Review: 'Bloodmasque' Carl Lyon Thursday, September 5, 2013 - 11:00am up11 With the App Store being absolutely flush with zombie games—much like the rest of the industry—it’s incredibly refreshing to see some other monsters, in this case vampires, getting their time in the supernatural spotlight with Bloodmasque. Set in 19th century Paris, Bloodmasque tells the all-too-familiar (but no less satisfying) tale of a half-vampire hunter who joins up with a French rebellion to undermine and overthrow a vampire dynasty that keeps the City of Lights under its spell. The game sticks firmly to its guns in its audiovisual direction, with the game’s Parisian landscape seeming almost like an interactive Les Mis, complete with jaunty string-and-accordion soundtrack. On the surface, Bloodmasque feels much like Infinity Blade or any number of other swipe-to-attack combat games. Tapping your foes will unleash a flurry of attacks, and swiping the screen allows you to dodge around them. Eventually, after chipping away at their health enough, they blow out of their waistcoats to reveal their more ghoulish countenances so you can continue the process, until you finally get to drive a stake through their heart in a ridiculous, oh-so-Japanese display of impalement. It works well, even if the touch-based combat is quickly becoming cliché in the wake of Infinity Blade. Where Bloodmasque sets itself apart in the single most ridiculous way possible is the ability to take a trio of pictures of yourself using your iDevice’s handy-dandy camera to be mapped to your character’s in-game face. I don’t post screenshots in my reviews very often, but it needed to be done so I could show you the glory of this: Sorry ladies, but I’m spoken for, and possibly quite drunk when I took that picture. The technology is still a little flakey (I, for the life of me, could not get my schnoz to line up with the geometry of the character model) but there’s some completely ridiculous fun to be had in trying out the ability to texture-map your puss onto your in-game avatar. The other interesting addition comes from the game’s unique take on multiplayer. Instead of being actively pulled into battles with other players, your avatar and its stats are put up for grabs on a roster, allowing other players to use you in battle, earning you valuable blood and bonuses even when you’re not playing the game. If there are any complaints to be made about Bloodmasque, the game’s dubious use of in-app purchases is rather grumble-inducing. Like many games on the App Store nowadays, there is the carrot-on-a-string tactic of offering in-game currency in exchange for real-world dough. This makes perfect sense in a free-to-play game, but it seems a bit swindly in a game with the (relatively) premium price of $6.99. Also, there is a certain degree of sameness between many of the game’s vampiric enemies, especially when they shed their human facades for one of a small handful of more monstrous forms. However, there is no requirement for players to pony up the extra dough, and the game’s bite-sized bouts of bloody battle mean that, unless you’re playing a marathon session, the repeated character models aren’t a real sticker of an issue. What’s left behind is a deliciously melodramatic slice of European gothic horror that takes itself seriously enough for deeper consideration, but is irreverent enough to fit its bathroom-break structure. View the discussion thread. View the discussion thread. <none> <none> Tonight on FEARNET TV review, ios games, bloodmasque, Square Enix, iphone, ipad, Vampires <none> <none> <none> FEARNET is a registered trademark of Horror Entertainment, LLC. © 2014 Horror Entertainment, LLC. All rights reserved.

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PERSPECTIVE: ON MOVING THE WORLD SEPTEMBER 01, 1991 by DOUGLAS MATACONIS Every so often, an event occurs that stands as a monument to the continuing struggle for human freedom and serves as a reminder to all who work for liberty that even when success seems farthest from reach, they can make a difference. Whether it is the Boston Tea Party, the storming of the Bastille, the Warsaw Ghetto uprising, or the assault on the Berlin Wall, such events are a vivid reminder that man has an undying desire to be free. Of all these, however, there is one event that will stand alone as the simplest and yet most profound reminder not only of the universal desire for liberty but also of the power of a single individual. This event occurred on June 5, 1989, one day after the Chinese government massacred thousands of its own citizens in Tiananmen Square. As a column of tanks rolled down the ironically named Boulevard of Heavenly Peace, a lone man ran into the middle of the street and stood in front of the lead tank, preventing the entire column from moving. For one brief moment, the age-old historical struggle between the individual and the state was crystallized into the image of this one man standing perfectly erect, staring straight ahead, with the gun turret of a tank pointed at him. It is said that the quest for freedom is the struggle between the armed state with its ultimate resort to the power of a gun and the individual with often nothing more than his principles to defend him. Never before has one event so perfectly represented this struggle before the world, and never before has the power of principle and the impotence of force been more perfectly communicated. To those who fight the daily battle for liberty on even the smallest, most inconspicuous, and sometimes apparently the most meaningless level, the actions of this man in Beijing should serve as an inspiration and a reminder that, though a single individual may seem powerless to change anything, the greatest success must always begin with someone who is willing to stand up and fight for what he believes. Where, after all, would the world be today were it not for the first American patriot who resisted British rule, the first Frenchman who stood up against the ancien régime, the first person who refused to comply with the Nazis’ plan to murder every Jew in Europe, or the first East European who demanded his freedom in the worst days of Communist tyranny? At the time, it may have seemed to all of these people that they were engaged in a hopeless exercise, that the resistance of one man is nothing compared with the military and political power of a state. They acted not because they knew that they would win, for victory was far from certain, and not as part of a mass struggle against tyranny, for they were, at least initially, quite alone. They acted because they knew they were right, because they wanted to be free, and because they hoped that by taking a stand they would inspire others to do the same. History, of course, proved them correct in the long run—acting alone they not only inspired others but eventually proved victorious. The undeniable lesson of history is this: One person, backed only by the strength of his convictions, can make a difference; one man can change the world. —Douglas Mataconis George Mason University School of Law Balance of Trade Imagine applying mercantilism to our everyday economic affairs. When our employer gave us our weekly paycheck, we would have to say that this was a favorable balance of trade since it ended up with us having more money at our disposal. On the other hand, we would have to speak of being victimized by an unfavorable balance of trade when we shopped at the supermarket. This is because money left our hands and went to the grocer. But anyone who has ever shopped realizes that gains are made by such activities. Who would patronize the local supermarket unless what they get is worth more to them than what they pay for it? It is the same with nations. If we buy more this month from Japan than we sell to them, this doesn’t mean we are exploited by them any more than grocery stores victimize us when we shop there. More to the point, the purpose of trade is to import—just as the purpose of working is to be able to afford to buy or import the groceries. So the next time you hear that we have a negative balance in merchandise trade, remember that means we are consuming more goods and services provided by foreigners than they are getting from us. —Walter Block writing for The Fraser Institute Vancouver, Canada “No Problem” “You want to go para-sailing?” the pilot of the snorkeling boat asked as we pulled ashore near Montego Bay. “No problem.” And there was no problem. He hailed a cab, the driver took us a few miles down the sandy Jamaican beach, we paid cash, signed a one-paragraph release, and we were up in the air. It was as simple as that. It’s about the same if you want to take your first scuba dive in Aruba. You sign a release, they sit you down to explain the basics, you practice in a pool, and an hour later you are diving off the side of a boat. Again, “No problem.” Unfortunately, it isn’t so easy if you wa

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For over a half century (and three generations) Felicia has hosted entertainment celebrities, sport figures, polticians and tourists visiting the North end of Boston, and a multitude of neighbors and friends. Although she has inspired many imitations, Felicia’s remains the orginal. We are proud to bring to Stoneham Felicia’s fine Italian cooking.

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First Revised Volume No. 1 Effective Date: 09/30/2010, Docket: RP10-1032-000, Status: Effective Original Sheet No. 131 Original Sheet No. 131 Sign and fax this Agreement within 3 days to: Director of Marketing, Caledonia Energy Partners, L.L.C., Nominations/ Notices hereunder via Caledonia website and phone: Hub Services Manager Long-Term Hub Services Manager CALEDONIA ENERGY PARTNERS, L.L.C. By: Enstor Operating Company, LLC, its Manager By: ___________________________ Title: __________________________ Notice Address: 20329 State Hwy 249, Suite 400 CUSTOMER: ______________________________ By: ___________________________________ Name: _________________________________ Title: ________________________________ Notice Address: _______________________

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FightHype Community > OTHER HYPE > General Discussion Does Anybody Here Have Dogs??? I've been a dog owner for the better part of 11 years, but as 3 of weeks ago, I bought two new pups from some people in the parking lot of a tire shop. They had SEVERAL pups, but I only needed 2. One is a Jack Russell Terrier (female) and the other is an American Bulldog (male). I'm almost inclined to believe that they're mixed, but hell, I saw Labs and a couple of other breeds around the same age as them for sale, so who knows. I had them for 2 days, and the female ("BB"...that's the only name that she responds to IF you say it FAST) ended up getting the parvo virus. It was BAD man, like real bad. Constant vomiting, diarrhea, refusing to eat AND drink, lazy, sleeping all day...it was horrible. The virus itself doesn't kill the dog, but the dehydration part that comes along with the symptoms, is what does the trick. I took her to the vet, and these sacks of shit didn't even test her for parvo. They gave me antibiotics, a booster shot in the ass, something else for worms...and sent me on my way. I thought that she would be okay, but it got worse (same symptoms). I was working crazy hours that week, so my mom came and picked up both of them. She ended up taking them to the Humane Society for treatment, which cost about $75 per day. They gave her an IV in her back, which left a huge quasi moto-type hump in her back and allowed the fluids to spread around her body after a couple of hours. Then they gave her a shot for anti-diarrhea, anti-vomiting, and some other shot. 3 days of that ($225 later), and she was back to her hyper self!THEN, the male dog (Bruno) caught it because they were around each other most of the time (except the last 3 days). Unfortunately, he didn't make it, as of last Friday. (IMG:style_emoticons/default/no2.gif) He went to vet for the same treatment for 5 days ($375), but he was just too small to fight it off. I watched him have a seizure, lose movement in his legs, struggle to breathe, and ultimately, I left my parents house when I saw that his eyes would barely stay open as he transitioned. With that in mind, I waited til today to find the people that sold them to me ($125 each), and explained what happened to Bruno. It took EVERYTHING inside of me to not do some stupid shit that would involve bail money. By the end of the explanation, I walked away with a free pup...which was again, an American Bulldog (male). I may just name him Bruno...and start all over. I have "the Bruno of old's" ashes here with me...poor little fella. Anyhow, this new pup is damn near a mirror image of Bruno! Too funny. Parvo is some serious shit, and it stays in the environment for YEARS. I actually bleached my whole yard (front and back), by deck in the back yard, and a few other things. I bleached the remaining carpet in my house, and I'm thinking of things that they both touched when they had parvo. The ONLY thing that will kill that virus, is bleach. Anyhow, the new pup (may as well name him Bruno too), will be going to the vet for tests, when the roosters crow (do they crow?), and he'll remain in the house for about 3 or 4 weeks. He's only about 8 or 9 weeks old, while BB is about 11 weeks old. She's doing good with being outdoors, but I haven't let her step foot off this disinfected property.Speaking of BB, this freakin' dog is handful! I actually read some stuff on how to train them, and I was in for a HUGE shocker. Come to find out, these fuckin' dogs have a high success rate!....a high success rate in training the fuckin' trainer, rather than being trained. What have I gotten myself into?We've had a looooong week, but I'm sure she knows who's boss at this point. I still can't trust her out of my sight, nor will I...for maybe another 4 or 5 years. I had JUST taken her outside to use to restroom (for 15 mins)...nothing. So, she races back inside, and runs in my room. I just repainted my room, so my curtains are on the floor...guess where she decided to leave me a gift? Yep, you got it...on my fuckin' curtains...a nice, hot steaming pile of shit. I'm glad I got a new pup today, so she can at least be kept some type of company. I'm still working on her restroom timing (which is going well), but she knows when to press my buttons for attention, and it's USUALLY when I'm doing something that I like doing around here (watching tv, home projects, etc). Never when I'm washing dishes or any other ass-chapping chore around here, will she give me a run for my money. (IMG:style_emoticons/default/laugh.gif) Posts in this topic Cshel86 Does Anybody Here Have Dogs??? May 12 2013, 06:24 PM aTYpicalTYrant Man I'm sorry to hear that. I'm a dog love... May 13 2013, 07:41 AM Cshel86 QUOTE (aTYpicalTYrant @ May 13 2013, 08:4... May 14 2013, 09:44 AM daprofessor sorry to hear about the pup. best thing u can do f... May 22 2013, 02:44 PM Cshel86 This is BeBe (you have to say her name fast, lol),... May 22 2013, 03:11 PM csrighthook Sorry to hear about your pup, I'm a dog lover ... Jun 15 2013, 07:09 PM daprofessor QUOTE (csrighthook @ Jun 15 2013, 07:09 P... Jun 18 2013, 04:58 PM Cshel86 Bumped Aug 20 2013, 02:08 PM

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Login Join C- Movie Trailers Movie Photos Comments 12 Monkeys Movie Review The sci-fi genre... aliens, space travel, phenomenons... and time travel. That's what 12 Monkeys is about: time travel, although it's not as sci-fi related as it appears. Bruce Willis is a time traveler, which makes 12 Monkeys a sci-fi movie, but the entirety of it is not as complex as one would think. In fact, every scene that takes place in 2035 is just a souped-up shell that makes 12 Monkeys look a lot more technical than it is. In 2035, all the "volunteers" are in tiny, wire cages and are lifted up and out with cables. The world above is devoid of human life, but wild animals like bears, tigers, and spiders run wild, and below is where the humans live. For some reason, the entire underground system looks like an alien spacecraft, for reasons unknown - it does not look like humans constructed it. This was just the first attempt at making a movie look more interesting than it really was. Bruce Willis travels back in time - too far back in time - and is admitted to a mental hospital. All the people there are totally wacky, including Brad Pitt, who begins to get annoying after three minutes. I don't really understand why they chose to have Pitt, who has more to do with the movie than at first glance, be a mental patient, unless it's to express his psychotic nature. However, other movies have made psychotic characters effective without introducing them in a mental hospital. When he goes back again, it is in 1996 (after taking a quick stop at World War I), and that is where the rest of the movie takes place. Madeline Stowe's character becomes more important than earlier and ends up being the best character out of the movie: smart, beautiful, but a little helpless. She begins to realize that Willis is telling the truth, so she defies the police and helps him look for The Army of the 12 Monkeys. Unfortunately - I warn you, this is going to be a spoiler - the 12 Monkeys may be responsible for all the wild animals in the city, but apparently have nothing to do with the virus at all. Worst off, I don't know if Willis even accomplished anything by the time the movie was over. The ending was interesting but definitely not something I expected; it was rather disappointing. And the little carnival sound track was incredibly stupid. 12 Monkeys had all the potential in the world but no more than ten minutes of it deserves recognition.

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Firehouse Expo Instructor Saves Wife When Tony Tricarico got the call Thursday morning from his wife telling him she was trapped in a hotel elevator, he thought it was a joke. Standard Will Change Thermal Imagers BALTIMORE, Md. -- The current inventory of thermal imaging cameras available to departments can be confusing to navigate due to unique features on each model.With the creation of NFPA 1801 -- released at the beginning of this year -- this should soon... Coordination Between Fire, Police Has Improved Since Columbine Shooting BALTIMORE, Md. -- When the first responders arrived at Columbine High School in Littleton, Col., they had no idea of the magnitude of the event.Firefighters and EMTs stopped in front of the school where students were running toward them. They found a... Expo: Level Funded Budget Is a Win Lt. James Kirsch of the Bergenfield (N.J.) Fire Department said there's no panacea, or magic bullet, that will miraculously make fire departments' economic woes disappear. He does, however, have a bunch of tips to help lessen the pain. " In these tough... News • July 23rd, 2010 Baltimore Welcomes Firehouse Expo Firehouse Expo 2010 officially opened this Wednesday in Baltimore, Md. L.A. County Chief Recalls Haiti Rescues He said the lessons learned can be applied to disasters that occur in the U.S. Injured New York Fire Chief to Talk About Need to Buckle Up at Firehouse Expo On Thursday morning during opening ceremonies at Firehouse Expo in Baltimore, Eddie DiMartino and his wife will discuss the ramifications of his decision not to buckle up. Fireworks Safety for Firefighters When it comes to professional fireworks displays, there are some important things firefighters need to know to keep themselves and the public they are sworn to protect safe. Chicago Fire Department Works to Address Suicides Between the beginning of 2007 and the middle of 2008, the Chicago Fire Department experienced a growing number of suicides within its ranks. Education is Key to Infection Control For more than 35 years, Katherine West has been involved with infection control and was a pioneer in education for emergency medical service personnel.After all those years involved with educating providers West said it's "abundantly clear that... Firehouse® Roundtable: Apparatus Maintenance Fire apparatus and emergency equipment must respond in extreme heat, bitter cold, flooding, dusty conditions, over pothole-filled roads — you name it, it's got to be able to get there. Firefighters and first responders are like the letter carriers of... L.A. Fire: ‘Pranks to Professionalism’ Firehouses across America are hotbeds of pranks and practical jokes, and many say it’s the culture of the fire service. Some say firefighters just need to learn to deal with it, but there’s a growing segment who say pranks have no place in a... 'Everyone Goes Home' Promoted in Indy Firefighters don't usually go to work each day thinking that this may be their last day alive, but the reality is, it could be. That's why it's important to do everything one can to prevent firefighter line of duty deaths. That's why it's the mission of... FDIC Panel Debates Issue of Diversity When it comes to diversity in the fire service, it's ironic that there are many divergent opinions about what that is, and just as many on how to achieve it.A panel discussion conducted a courageous conversation on diversity at the Fire Department... FDIC Spotlights Firefighter Free Speech What would you do if a firefighter came into your station sporting a brand new tattoo with KKK written on his bicep - and he is a white captain supervising a predominately black engine company? Could you, as a chief, ask him to cover it up? What about...

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Five Species of Shark and Two Manta Ray Species Now Protected by CITES Conference in Thailand breaks wall set up by those opposed to protections of shark species that are captured and finned. Giant manta ray (Manta birostris). Photo by Jon Hanson/Wikipedia Five species of sharks and two species of manta ray were given trade protections during the 16th Convention on International Trade in Endangered Species of Wild Fauna and Flora that just concluded in Bangkok, Thailand. The vote two-thirds vote from the 177 CITES member governments puts the number of shark species protected by CITES to eight. The new additions to the list include the oceanic whitetip (Carcharhinus longimanus) and porbeagle shark (Lamna nasus) and three species of hammerhead shark, the smooth hammerhead (Sphyrna zygaena), great hammerhead (Sphyrna mokarran), and scalloped hammerhead (Sphyrna lewini) shark. The protected manta rays are the oceanic manta (Manta birostris), and reef manta (Manta alfredi)."This is a major win for some of the world's most threatened shark species, with action now required to control the international trade in their fins," Susan Lieberman, director of international environment policy at The Pew Charitable Trusts said in a statement released by the Trusts. "This victory indicates that the global community will collaborate to address the plight of some of the most highly vulnerable sharks and manta ray species. Today was the most significant day for the ocean in the 40-year history of CITES."Would You Like to Learn More?Thousands of Shark Fins Drying on Hong Kong Rooftop Causes OutcryTwo Million Square Mile Shark Sanctuary Established in the Western Pacific OceanRosie O'Donnell Gets Flack for Hammerhead Shark PhotoLieberman also said that the gridlock created by those countries opposed to the listing of these species has been broken. Sharks have declined by as much as 90 percent in some areas of the world due to the practice of finning, in which sharks are taken from the ocean, their fins removed and the shark thrown back to sea. The fins are then sold in China and other countries in Asia, the United States, and around the world as the main ingredient for shark fin soup. Manta rays have been killed for their gill rakers, which are used to filter food from the water column, to make a so-called Asian “health tonic” that has not been proven to aid in any health malady. The trust also said that now that the commitment to protect these species is on the books, the regulations must be fully implemented and enforced to ensure that these animals recover to ensure a sustainable future for them as well as the larger marine ecosystems that are dependent upon them for the overall health of their environments. Sharks have been disappearing at alarming rates worldwide. The International Union for Conservation of Nature says that 143 species of shark are threatened with extinction, largely due to human factors such as finning. It is estimated that more than a million sharks are killed each year by fisherman who fin them and throw the still live shark into the ocean to drown. That estimate is a conservative one. Some estimate the number of sharks killed each year at close to 250,000. Give us your opinion onFive Species of Shark and Two Manta Ray Species Now Protected by CITES

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Edinburgh International Film Festival 2013 – Not Another Happy Ending (2013) June 29, 2013 by admin Leave a Comment Not Another Happy Ending, 2013. Directed by John McKay.Starring Karen Gillan, Stanley Weber, Gary Lewis, Amy Manson, Henry Ian Cusick, Kate Dickie, Freya Mavor, and Iain de Caestecker. Karen Gillan stars as Jane, a budding Scottish writer who gets writers block during her second novel. Having been advised that the trailer for this film gives away the ENTIRE plot, I went into the cinema unprepared, armed with only a brief synopsis and the belief that the wonderful Amy Pond of Doctor Who couldn’t possibly disappoint. To be fair to Karen Gillan, she didn’t disappoint in the slightest. She was frank, quirky and witty, with excellent Pippi Longstocking braids of thick red hair. Unfortunately, the rest of the film proved too heavy for her to carry alone, and it fell disastrously flat. The male lead is Tom Duval (Stanley Weber), a passionate Frenchman who gives Jane her big break. The set up between the two was so obvious it was a little painful to watch; a pain that was not relieved by either clever script or sparkling chemistry. Honestly, I don’t think I’ve ever seen an on-screen pair fancy each other less. Yet more disappointment lay in that the plot gave us absolutely nothing of substance to distract from the clumsy progress towards guy-gets-girl. Attempted sub-plot number one: Jane is haunted by her protagonist while suffering from writers block. What could have been a really excellent look at the relationship between a writer and her characters (see Stranger Than Fiction) was instead very ill used – ‘Darsie’ popped up once in a while to be provoking, and occasionally served as a foil to Jane’s thoughts, but accomplished no other purpose. Attempted sub-plot two: Jane’s relationship with her father. Her first novel, a pseudo-fictional account of her disastrous childhood, is a roaring success, and brings her absentee father back on the scene. The atrocities she endured as a child are consistently alluded to, but the script is gravely lacking in any exploration of how they affected her, other than to mention she ‘worships her pain’. This statement is supported by one haphazardly included wall of rejection letters at the very beginning, and nothing else – Jane is otherwise quite a merry and well-functioning person. All in all, a poor script and poor casting choices leave Karen Gillan floundering to give a performance with any kind of meaning or depth, and it’s a great shame for what is her feature film debut. I hope her next film, Oculus, does not leave as much to be desired. Flickering Myth Rating - Film ★ / Movie ★ ★ Samantha Morrison Filed Under: British Film, Edinburgh Film Festival, Festivals, Reviews, Samantha Morrison Around The Web

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Meltzer’s Musings: Final Day of World Championship Prelims, Mark Alt Posted on May 14, 2013 by Bill Meltzer TUESDAY ROUNDUP: FLYERS AT WORLD CHAMPIONSHIPS Today is the final day of the preliminary round of the 2013 IIHF World Championships. The top four teams in each bracket will move on the medal round quarterfinals. The last place finisher (Slovenia in one bracket, and Austria in the other) will be relegated to Division IA next year, being replaced by Kazakhstan and Italy in the 2014 Worlds. The re View original post here: Bill Meltzer

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Richard J. Daley Center Chicago Sights Fodor's Chicago 2014Trade Paperback Richard J. Daley Center Architectural Sites | Chicago | The Loop Richard J. Daley Center Review Named for late mayor Richard J. Daley, this boldly plain high-rise is the headquarters of the Cook County court system, but it's best known as the site of a sculpture by Picasso. Known simply as the Picasso, this monumental piece provoked an outcry when it was installed in 1967; baffled Chicagoans tried to determine whether it represented a woman or an Afghan hound. In the end, they gave up guessing and simply embraced it as a unique symbol of the city. The building was constructed in 1965 of Cor-Ten steel, which weathers naturally to an attractive bronze. In summer the building's plaza is the site of concerts, political rallies, and a farmers' market on Thursdays; during the holidays, the city's official Christmas tree is erected here, and Christkindlmarket, a traditional German market selling food and gifts, takes over the area. Address: 50 W. Washington St., Loop, Chicago, IL 60602 | Map It Hours: Weekdays 8–5:30 Website: www.thedaleycenter.com Location: The Loop · Map of Richard J. Daley Center · Browse Chicago sights Far North and Far Northwest Sides Pilsen Prairie Avenue Combating Cabin Fever: An Escape to the Windy City (Chicago with Pre-Teens) Where: Chicago with a friend and her pre-teen daughters When: Two days in February 2014 Why: After being housebound by what seemed to be a never-ending winter (enough already!), it was time to bundle Read more Aussies' USA "White Xmas" 2013/14 Trip Report In December 2013/January 2014 my wife and I did a three week trip to the USA, with the aim of experiencing a proper North American winter. Read more ·Illinois Forum Chicago and Where Else We've never been to Chicago other than changing planes. We'd like to go for a few days but that's a lot of flying to spend 3-4 days in one place. Any add-ons in the area? Thanks. Read more Wine and Cocktails Where to Drink in Chicago Now With more and more bars opening up around the city, Chicago is proving it knows its way around a cocktail ... Read more Spring 2014 Guide to Chicago The Windy City is home to a slew of new restaurants, boutique hotels, and museum exhibits worth checking... Read more Deals, Hotels 6 Hotel Deals for Martin Luther King, Jr., Weekend A getaway over Martin Luther King, Jr., weekend (January 17–20, 2014) proposes the perfect remedy... Read more

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Carlsbad Caverns National Park > Sports and Activities in Carlsbad Caverns National Park Carlsbad Caverns National Park Sports and Activities Bird-Watching

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Toyota Recalls 150,000 Tacomas on Corrosion Concerns Rich Smith | Toyota Motor (NYSE: TM ) today announced a voluntary safety recall on some 150,000 Tacoma pickup trucks from the 2001-2004 model years. According to the company, spare tires on these trucks are stored underneath the rear bed on spare tire carriers on metal lift plates. These lift plates, however, "may not have been sufficiently coated with phosphate" at the time of manufacture, making them vulnerable to rust when driven in "cold climate" states where salt may have been used as an ice preventative in winter. The company warns that "over time and in limited cases, corrosion of the lift plate could cause it to break and result in detachment of the spare tire from the vehicle." The company is recalling the trucks in question to ascertain the extent of such corrosion and, if necessary, to repair the defective part at no cost to the owner. Targeted at trucks bought or registered in the District of Columbia and 20 "cold climate" states -- Connecticut, Delaware, Illinois, Indiana, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Virginia, Vermont, Wisconsin and West Virginia -- the recall will probably extend across the length and breadth of the U.S., given the long time between manufacture and recall, and the likelihood that cars originally sold in these 20 states have since migrated elsewhere through the resale market. Wherever they live now, owners of the affected vehicles can expect to receive letters from the company notifying them of the recall beginning in December 2012. Fool contributor Rich Smith has no positions in the stocks mentioned above. The Motley Fool has no positions in the stocks mentioned above. Try any of our Foolish newsletter services free for 30 days. We Fools may not all hold the same opinions, but we all believe that considering a diverse range of insights makes us better investors. The Motley Fool has a disclosure policy. Toyota Motor Corp…

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FA targeting Euro 2020 openerTweetMoreThe Football Association is bidding to bring the opening game of Euro 2020 to Wembley.It was already known that the FA was keen to bring the final to England's national football stadium, but the first match also carries high prestige.FA general secretary Alex Horne told The Times: "On the basis that someone needs to stand up, we have done it."It's a big game, the opening game. It would be great for London, for Wembley. I pushed it to UEFA, quietly at the moment, but we are going to make a play for it with our bid."The UEFA tournament will be staged in cities across Europe, rather than being held in one or two countries as has been the norm.Istanbul has been widely viewed as the favourite to be awarded the final, with a decision on venues expected to be announced in September of this year.Horne's focus in the early part of this summer will fall on the World Cup, as England head to Brazil.Group games against Italy, Uruguay and Costa Rica could make it difficult for Roy Hodgson's team to go beyond the group stage, but the FA general secretary has firm belief in the manager's ability.Hodgson signed a four-year contract when appointed in 2012 and Horne is certain the former Fulham and Liverpool manager will be the right man to lead the mission to Euro 2016 in France.He said: "For me personally, Roy is our manager to France and I'm happy with that, very happy with that. I think he's been brilliant. He's exactly what we hoped for."Horne insists Hodgson has already achieved a "pass mark" by guiding England through qualifying."For me personally, he's done it by getting through that group," said Horne. "We go optimistic that we are going to enjoy it and play well."Horne also suggested it would be "possible in the next five years" for Wembley to be home to an NFL American football team. The stadium has already staged matches in the NFL season, and is due to hold three matches later this year.Horne said: "You may see a franchise discussion come up. There is a big question about whether we can house a franchise alongside England in the autumn. That will be really interesting. It would need an owner to do it."Horne even believes Wembley could stage the highlight of the NFL year."Then we can get the Super Bowl," he added. "You don't rule anything out."

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16 Conclusions On Chelsea 2 Liverpool 1 Liverpool have a serious problem with holding on to the lead in the 'big' matches, while Chelsea delivered their most impressive display of the season so far...

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Flamini hails Arsenal edge Mathieu Flamini feels Arsenal now possess the 'physicality' needed for a Premier League title challenge. Mathieu Flamini: Pleased with how Arsenal's season is going The French midfielder returned to the Gunners on a free transfer from AC Milan in the summer, and while record signing Mesut Ozil has captured many headlines, Flamini's presence has been equally impressive. Flamini now believes that Arsenal are ready to end their nine-year wait for silverware, and that could possibly be in the shape of the Premier League title. "What you need in any Arsenal side is the fighting spirit and you can see we now have that," Flamini told the Daily Star. "Perhaps the physicality has been missing a bit in the past few years. "But if you want to win leagues and cups, sometimes you have to fight for it, especially when you are playing in the hardest league in the world. "We have a very good offensive team but it is so important to be strong defensively as that could make the difference at the end of the season. "You have to go to places like Newcastle and be prepared to fight before playing your football. Only by doing that can you win. "Picking up three points to return to the top of the league was a fantastic feeling. The team spirit was amazing and there was so much fight. "Everyone fought for each other and that is what got us through. We are top of the league at half-time and we would have signed up for that at the start of the season. "We know this is a marathon, a long burner. We have to stay very focused and work as hard as we did at Newcastle. That's all we can do."

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AVB expects Bale move 'very soon' Tottenham boss Andre Villas-Boas says Gareth Bale could move to Real Madrid "very, very soon". Last Updated: 28/08/13 at 17:04 Post Comment Tottenham Specials 13/14. Click here to bet. RSS Feed Gareth Bale is close to sealing a world-record move to Real Madrid - but he looks likely to leave Tottenham with a hefty fine after angering manager Andre Villas-Boas with his conduct over the last few days. After two frantic months of speculation, negotiation and gossip, Villas-Boas confirmed today that Tottenham and Real Madrid are nearing agreement over Bale's world-record transfer to Spain. The Tottenham manager said the transfer could happen "very, very soon" and it also emerged that Bale bade farewell to his team-mates last Friday. Spurs and Bale both wanted the transfer to happen without any acrimony, but that has simply not been possible. Villas-Boas often spoke about his strong relationship with Bale last season. Their warm embrace following Bale's stunning winning goal against West Ham proved they were close. That relationship has now broken down, however. Villas-Boas has remained calm throughout the whole saga, but today he made no secret that he has become fed up with Bale's conduct. Villas-Boas is unhappy Bale has not turned up to training for the last two days. He thinks the Welshman chose to do so in order to try to push through his move to Spain and it appears he thinks Bale should now be hit with a fine. "The fact that he hasn't turned up, I don't think it's the correct behaviour," the Tottenham manager told a press conference that was called to preview the club's Europa League game against Dinamo Tbilisi. "It's a position of pressure and a statement from the player. "It's a position they chose to take. It's up to the club now to decide if it's a fineable offence. "It's up to the club to decide whether or not it's a breach of club rules. "I've given my opinion on it, it's up to them to decide whether they act on it or not. "It is a dream move for him but I think in the end this could have happened in a different way." Under PFA rules, a player can only be fined two weeks' wages, which in Bale's case amounts to around £160,000. The Tottenham hierarchy will discuss whether to hit the player with the sanction in the coming days. By the time that fine lands on Bale's doorstep, he looks likely to be in Madrid, however. Villas-Boas has refused to reveal much about Tottenham's dealings with Real throughout the summer, but today he was much more forthcoming about the state of play. "At the moment the two clubs are speaking to outline the final decisions or statements of contracts," Villas-Boas said. "It could happen very, very soon. I suppose it could go to the last days or it could happen in the next two days." "There will be a three-way agreement for the player to go and Tottenham will accept most likely the biggest transfer in world football. Then it will be the end of story." Villas-Boas usually cuts a diplomatic figure in front of the press, but today it was clear he cannot wait for the Bale saga to end. The Portuguese hit out at Real Madrid for their conduct during the transfer, and he also surprisingly lambasted Roy Hodgson over his decision to select Andros Townsend for England. There even seemed to be a little dig at chairman Daniel Levy over his failure to speak publicly about the transfer. After spending weeks being peppered with questions about Bale, Villas-Boas' frustration was clear when he was asked to confirm whether other clubs had bid for Bale, as had been reported earlier this week. Villas-Boas said: "It's not up to me to confirm that... I'm not sure if... the chairman will be (in) the ideal position. Obviously he doesn't sit in this chair to speak to you very often, or never." Tottenham have already spent a vast chunk of the £86million they are expected to receive for Bale. Four signings have already arrived and there could be more than three new faces in the squad by the time the transfer window shuts on Monday night. Villas-Boas, who has recorded three straight wins without Bale, is sure his team will be able to cope without a man who scored 26 goals for the club last term. "We have a very, very strong team the same," he said. "If this transfer happens, it will give the opportunity for others to step up their game and I think we have seen that in the last couple of games. "There has been no disruption. We've been working well, the team is training very, very well and we have had three wins." Tottenham are in talks with Roma and Ajax over the potential signings of Erik Lamela and Christian Eriksen respectively. Vlad Chiriches is expected to complete his move to Spurs from Steaua Bucharest by the time they face Arsenal on Sunday, but Villas-Boas says even more targets could be signed after that. "We will continue re-strengthening the squad," he said. "Not only those players, others as well." Villas-Boas believes there is no chance of Spurs signing Chelsea midfielder Juan Mata, though. "Chelsea wouldn't sell to Tottenham in any way or form, as they think that we are title contenders," Villas-Boas added. Sky Bet Free Bet Club: £10 free bet - £5 free every week Rennes survive scare Arsenal 8/13 for top-four finish Dortmund reach DFB-Pokal final Performances not goals for Stokes Anfield pays Hillsborough respects Pellegrini not giving up on title Everton to edge closer

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Help | Connect | Sign up|Log in Rebecca Ruiz World's Most Endangered Coastlines The consequences of climate change in coastal regions include stranded polar bears in the Arctic, a sinking island in the South Pacific and frequent tropical storms that batter the Caribbean. Over-fishing and pollution also significantly harm coastal regions by wreaking havoc on the ecosystem. Many of the changes that occur as a result, like so-called dead zones, where oxygen levels drop to below the amount necessary for aquatic life, and depletion of the fish population, are not readily visible but still pose a long-term threat to the viability of a coastal region. Also at stake is a billion-dollar tourism industry. In Pictures: World’s Most Endangered Coastlines Beach tourism accounts for 9% of domestic trips in the U.S., according to the Travel Industry Association, a non-profit trade group. The United Nations World Tourism Organization does not track coastal tourism spending, but its research has shown that the world’s most popular destinations are coastal countries such as Spain, Italy and Mexico. In 2006, international tourism receipts reached $733 billion. Threats To Coastal Regions That money may not make it to some spots much longer. Tourists enjoying the panoramic views of the Caribbean, Central Chile or the Gulf of Maine may not realize it, but each of these coastal areas is at risk of long-term change. The coral reefs of the Caribbean are whitening as a result of climate change; coastal development in the Gulf of Maine has led to the loss of hundreds of acres of highly-productive salt marsh; and aqua-farming in the coast of Central Chile has changed population levels of marine life. Related Stories Eight Hot Spots For Volunteer Travel How To Travel Well On A Weak Dollar These regions topped a list of threatened coastlines, according to a report on the human impact on marine ecosystems, released recently in the journal Science. The study looked at a number of factors, including fishing, pollution and sea temperature, but did not consider the impact of coastal development. Scientists are still trying to understand the consequences of human impact but know they can range from coastal erosion to the death of a marine species to the destruction of a coral reef. All of these have serious implications for the long-term health of a coastline. When the harmony of a coastal region is disrupted, it can lead to fundamental changes. A healthy coral reef, for example, can protect a coastline from storm surges. Dying fish populations can leave the coastline vulnerable to further ecological chaos. Mark Spalding, a senior marine scientist at the Nature Conservancy and a co-author of the report, says that population density, aqua-farming and coastlines engineered to accommodate development are “changing huge areas of the world’s coasts.” “The bigger problem is the amalgamation of threats,” he says. “One feeds off the other.” In the Caribbean, for example, the combination of over-fishing, coral disease, climate change and excess nutrients in the water lead to what Spalding calls a “synergy of threats.” Are you concerned with the effect of travel on the environment? Weigh in. Add your thoughts in the Reader Comments section below. Researchers found that recent cyclones near the island of Mauritius in the Indian Ocean, which killed or damaged coral reefs, could be attributed to climate change. In Fiji, which received more than 500,000 visitors in 2006 and earned $742 million from tourism, an increasing number of cyclones and storms have caused shoreline erosion. Stefanos Fotiou, tourism program officer for the United Nations Environment Programme, says that the travel industry must quickly assess the various threats to coastal areas. “They are creating a cost that the industry will be called to pay later,” he says of companies that resist initiatives to better protect the environment. Sustainable Coastal Tourism Those who are concerned are turning to sustainable tourism. The goal, according to the United Nations Environment Programme, is to both protect the ecosystem and ensure the long-term economic viability of tourist destinations. Sustainable tourism also gives consumers the power to influence the travel market. Brian Mullis, president of the nonprofit organization Sustainable Travel International, says that consumers’ choices can dictate business practices like energy efficiency, reduced water consumption, lower levels of waste generation and supporting local economic development. STI, which has about 400 active clients, provides consulting services to businesses interested in sustainable practices like these. “When quality or convenience is perceived as equal, the conscientious consumer will want something environmentally responsible,” Mullis says. In the Caribbean, home to 7% of the world’s coral reef population, there are increasing options to support sustainable coastal tourism. The Caribbean Tourism Organization, which has 32 member nations, assists hotel and tour operators with developing and sharing environmentally aware strategies. Over 50 area hotels are certified by Green Globe, a company that develops standards and measures indicators like conversation, waste management and energy efficiency, according to Mareba M. Scott, a sustainable tourism product specialist for the Caribbean Tourism Organization. Her advice to tourists is simple: “It’s all about research.” When traveling to coastal regions, Scott says, consumers should seek out hotels, tour operators, airlines and restaurants that incorporate sustainable practices and are accountable to outside certifying agencies. Of course, investigating risks to one’s favorite vacation spot is also important. After all, the stunning vistas often conceal invisible threats. Luxury travel guides, hotel reviews, destinations. Expert advice for the luxury traveler.

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Help | Connect | Sign up|Log in Dorothy Pomerantz, Forbes Staff I write about Hollywood and run the Celebrity 100 List. Hollywood's Top-Earning Couples The indisputable king and queen of the hip-hop prom are Jay-Z and Beyonce Knowles. The couple, who quietly married in 2008, not only produce and sing some of the biggest hits on the charts (including “Single Ladies” and “Empire State of Mind”) but they oversee clothing lines, perform around the world and endorse products from companies like American Express and Budweiser. All that hard work has paid off. Between June 2008 and June 2009 the couple earned a combined $122 million putting them squarely at the top of our annual Top-Earning Couples list. In Pictures: Hollywood’s Top-Earning Couples Video: Top-Earning Celeb Couples Our list includes actors, musicians and professional athletes. We talked to agents, managers, producers and lawyers to determine what celebrities earned from staring in movies, touring, selling albums, playing professional sports, creating lines of clothing and perfumes and appearing in ads. Jay-Z and Beyonce both contribute significantly to their joint earnings. Last year Beyonce out-earned Jay-Z, bringing in $87 million to his $35 million. (The couple also topped last year’s list with $162 million. About half of that came from each star.) For the couple in second place on our list, it’s more about his big payday. Harrison Ford and his girlfriend, Calista Flockhart, earned a combined $69 million, $53 million less than Jay-Z and Beyonce. Almost all of that came from Ford’s work in Indiana Jones and the Kingdom of the Crystal Skull. Ford and producers Steven Spielberg and George Lucas made a unique deal with Paramount on the movie that gave them a significant portion of the film’s earnings after the studio broke even. As a result Ford eared a jaw-dropping $65 million for putting back on Indy’s trademark fedora. Flockhart earns for her work on the TV show Brothers & Sisters. In third place: Brad Pitt and Angelina Jolie. The power couple earned a total of $55 million split about evenly between them both. Pitt had one of the biggest hits of his career last year with The Curious Case of Benjamin Button, and Jolie has embraced her inner action hero with 2008’s Wanted and the upcoming film Salt. Will Smith and his wife, Jada Pinkett Smith, rank fourth with $48 million. Smith is perhaps the last of the great movie stars. Even in recessionary times he still can demand a $20 million paycheck. Pinkett Smith has a burgeoning career of her own. She voices Gloria the hippo in the popular Madagascar films and last year produced The Secret Life of Bees. The Smiths would earn even more if we were including whole families. Their daughter, Willow, appeared in I Am Legend with her dad and did voice work with her mom on Madagascar: Escape 2 Africa. Jaden Smith costarred with his father in The Pursuit of Happyness and will star in the upcoming remake of The Karate Kid. Rounding out the top five are David and Victoria Beckham. The pair earned $46 million between June 2008 and June 2009. The vast majority of that comes from David Beckham, who plays for the Los Angeles Galaxy. He is also playing for A.C. Milan and could appear in his fourth World Cup this summer. In Pictures: Hollywood’s Top-Earning Couples Video: Top-Earning Celeb Couples

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Help | Connect | Sign up|Log in 85 Broads, Contributor How One College President Is Breaking Down Barriers For Women In Tech By Angela Haines Against a background of persistent high unemployment, tech jobs go begging. These days even traditional retailers seek engineers to upgrade their websites as online sales skyrocket. Facebook Facebook recently announced a major presence in New York searching for East Coast tech talent. The shortage of graduates in what is known as STEM—science, technology, engineering, and math, has become a national problem, drawing the attention of the White House last fall which sponsored its first ever science fair. But even when brainy high school kids gravitate toward STEM courses, their interest often wanes in college. One stubbornly undeveloped group who represent a minority in almost all areas of STEM is women. But a nationally recognized computer scientist, mathematician and educator is determined to reverse the trend. When Dr. Maria Klawe (pronounced Kla Vay) became president of Harvey Mudd College in Southern California five years ago, she embarked on a strategic effort, similar to an overhaul she led at Princeton in her former position there as Dean of Engineering, to increase the presence of women in STEM fields. At Harvey Mudd, one of the seven Claremont colleges, Dr. Klawe’s strategy has already produced dramatic results. When she arrived, 33% of the student body was female, but only 10% of computer science majors were female. Today, 42% of the student body is female, and 40% major in computer science. Females majoring in engineering now account for 37%, and in physics their number is just over 20%. Dr. Klawe knows the problem first hand. As she quips, her resume has been “full of firsts” for about 23 years. Before a stint as Head of the Department of Computer Science at the University of British Columbia, she spent eight years at IBM IBM, ending up as manager at IBM of Mathematics and the Related Computer Science Department at their Almaden Research Center; she then served Dean of Science at the University of British Columbia before she was recruited by Princeton. Currently, she also serves as one of 10 members of the board of Microsoft Microsoft. But she feels lucky to be president of Harvey Mudd, “a haven of geeky, science-tech kids who face a more challenging curriculum than at much bigger institutions,” she notes. Her strategic plan for STEM gender equality works on several fronts. The first project was to make recruiting materials more female-friendly and supportive. “We wanted to make clear,” Dr. Klawe says, “that we like well-roundedness, so we are interested in dancers and poets and musicians, who are also unusually good at math and science. We’ve also eliminated hazing and have become very good at nurturing.” Other changes include a curriculum revision, a program of paid research projects starting the summer after freshman year, and participation of women at national tech conferences. The reluctance of women to enter STEM fields seems to have deep roots — which often don’t disappear even in the face of success. One of Dr. Klawe’s favorite topics is what she calls The Imposter Syndrome. “Even women who get into MIT, and major in engineering,” she says, “often continue to second guess themselves, worrying that success was a mistake. So the first time they get a B on an exam, they switch to a major in the humanities. Yet males can get all C’s and think they’re doing great. It’s just normal for males to overestimate their success and for women to worry that they don’t deserve to be where they are. That insecurity often haunts them into their professional lives.” One professor who helped Dr. Klawe tackle the disparity by revamping the Harvey Mudd introductory computer science course is Christine Alvarado, an MIT PhD grad, who admits she had to learn how to navigate the “cultural divide” between men and women in science once she understood “you don’t have to stay up all night and work seven days a week to succeed because that’s not what I’m about.” Collaborating with three other CS faculty members, Professor Alvarado changed the first-year programming course based on Java, “which was frankly just not very practical,” to a more collaborative, problem solving course to offer students “creative opportunities to do what computer scientists really do.” It teaches the Python language which is easier to apply to Web development and develops skills that can be applied to engineering, math and other subjects. Also, the course is now divided into sections so that students who are experienced in programming don’t discourage less experienced but equally talented classmates. Another strategy with big impact, says Professor Alvarado, is taking first year students to attend the Grace Hopper Celebration, an annual conference of thousands of female computer scientists which showcases successful women scientists. “It’s really helpful,” says Professor Alvarado, “for very young women to see women on the stage participating in panels discussing how they can manage their careers and maintain a sense of balance in their lives.” Once the most despised course, says Dr. Klawe, “Introduction to Computer Science is now the most loved.” What gives a small college like Harvey Mudd with a total enrollment of only 750 students, the courage and determination to take on national problems of gender inequality in the sciences? Dr. Klawe credits her faculty because “we’re the only place in the country where you can teach this quality of student—we’re competitive with MIT, Caltech and Stanford—and be rewarded for teaching. That’s not to say we don’t value research, but if you’re a crummy teacher, I can tell you that you won’t get tenure here.” But the Harvey Mudd model is not lost on bigger institutions, which lose an alarming number of STEM majors after tough introductory courses. Duke, University of California at Berkeley, and Northwestern are already adopting some of the Mudd strategies. Meanwhile, Dr. Klawe mission continues, as she speaks out on the importance of gender equality at other universities, companies and industry events — whenever she is not rolling around campus on her beloved skateboard chatting up students. In 2006 Haines become founding director of Henry Hudson 400 New York, a project to commemorate the 400th anniversary of the historic arrival of Henry Hudson in New York. When that project ended in 2009, she became a managing director of Golden Seeds, an angel investing group that supports women entrepreneurs. Haines also blogs for The Huffington Post. Now with this new blog, wStartup.com, the plan is to broaden the mission to become a go-to resource for all of you. Busting the Myth That Women Aren't As Ambitious as Men Kathy Caprino Less Talk, More Action: 2012 Will Be The Year For Women In Tech “Hazing” at engineering schools? Laughable. dolorescruz A lot of universities talk about women in tech, but in terms of campus careers talk is all it mostly is. For example, the University of Colorado at Boulder brags that it has two female IT directors. But neither one has much hands-on technical history. Their degrees are not in tech, to the best of my knowledge they have never held a hands-on technical job, and they did not come up through the ranks and pay their dues in the IT profession the way many other female campus IT workers did. They were the mentees of a former [male] Associate Vice Chancellor who was technical. A comparison of the technical org charts over the last 10 years shows that the REAL women in IT, those with technical skills and duties, didn’t fare nearly so well, career-wise, in that same organization. Things are not always what they seem. Our students are smart enough to pick up on the underlying reality. valerieyoung GREAT post! The impostor syndrome is indeed alive and well on college campuses and all the more so among women in STEM fields. Not long ago I heard a post-doctoral student in astrophysics at Caltech say, “I figure if I can get a Ph.D. in astrophysics from Caltech, anyone can.” Things are not much different in the work world as evidenced by the 580 members of the Society of Women Engineers who registered for a recent webinar I conducted on women and the impostor syndrome – more the double the usual number of attendees. On one hand, women in STEM fields experience the same inner nagging voice as other high achieving women – and it should be said, some men as well – that says, “I’m not smart enough,” “I was just lucky,” and “The fact that I failed just proves I’m a fraud.” However, when you’re the first, the only, or one of just a few women or people of color in your class, job, or organizational level, you also have the added pressure of feeling like you have to represent not just yourself but your entire social group – pressure that makes you more vulnerable to the impostor syndrome. In fact a study of elite engineering students found that merely thinking about being in the minority relative to men led to palpable anxiety in women. If you’ve ever been the only woman in a professional setting you probably know that at best, you may feel self- conscious; at worst, intimidated. Add to that any assumptions that as a woman or a person of color that you got where you are solely as a result of affirmative action (which in the minds of some translates into the belief that you are automatically less capable) or that you cruised on the basis of good looks. Either scenario can undermine your confidence and up the pressure to prove yourself. If you don’t think numbers impact performance, think again. As researchers at Massachusetts Institute for Technology discovered, once the percentage of female students in a department rose above about 15, women’s academic performance improved.. All of this can make it hard sometimes for women in STEM fields to sort out, “Am I anxious about being in a male- dominated environment because I really don’t think I’m competent enough, or am I experiencing the normal stress that comes from feeling isolated?” The key is to understand that you can be perfectly competent and still experience stress in these situations. Klawe and others are right to zero in on women’s response to failure. To overcome the impostor syndrome means we need to adopt the more typically male attitude of, “Hey aren’t I entitled to make a mistake?” and to assert our right to fall as flat on our face as the next person. It’s a matter of women letting go of unrealistic self-expectations of perfectionism and the belief that we “should” know it all and learning to rebound from setbacks more quickly by both depersonalizing and learning from failure. At the same time, this notion that our success was just a fluke or that we need to know 150 percent to consider ourselves remotely qualified is not all in women’s heads. Research has found for example that people are more likely to attribute a man’s success to ability and women’s to luck. In other words, when he achieves a positive outcome it’s because he has “the right stuff,” but when you pull it off it’s because you just got lucky. Then there’s the old joke about how a woman has to work twice as hard as a man to be considered half as good. Somewhere along the line women added the punch line “Fortunately that’s not difficult.” Well, guess what? As it turns out, it really is. Despite the increase in the numbers of doctoral degrees for women in science worldwide, men still dominate the highest levels of academic research. When a couple of Swedish scientists dug for answers they found that in order to be awarded coveted research grants, women scientists had to produce 2.5 times more research and/or published work to receive the same competence scores as male applicants. It should be pointed out that in these studies and more, both women and men held women to a different standard. Finally to Dr. Alvarado’s point about not being willing to work 24/7, women’s definition of success is a factor in the impostor syndrome as well. That’s because women generally have a more layered definition of success that goes beyond the tradition male model of power, money, and status. It’s not that women don’t want these things, but not to the exclusion of things like meaning, contribution, and work life balance. This is important because when faced with the opportunity to achieve greater levels of success, hesitation can easily be confused with fear and self-doubt. In reality, there are any numbers of non-confidence-related factors that can make you reluctant to move ahead, including a mismatch between your definition of success and what is expected and the additional time demands that come with success. Once you’re aware of these things you can sort out for yourself, “Am I anxious because I don’t think you CAN do it, or do I just not want it?” For Forbes to shed light on a topic of importance to not only women, but to the economy as a whole is in striking contrast to the position taken by The Wall Street Journal which recently used a review of my book on women and the impostor syndrome with Crown Business to advance an agenda that essentially says the Maria Klawe’s of the world simply don’t know what they’re talking about. To be clear, no author expects every review to be positive, myself included. However, the WSJ reviewer was shockingly out of touch with the realities of professional women and in particular those in the STEM fields. For starters, despite the impostor syndrome being a highly researched topic, she insists impostor feelings don’t exist and instead accuses Pauline Clance and Suzanne Imes, the two highly regarded psychologists who named the impostor phenomenon 1978, of having “cooked up” the idea. Ignoring the kind of research I cited here on the persistence of gender basis, the reviewer insists that “the idea of female competence not being taken seriously is both wrong and laughable.” In fact, my pointing out the greater prevalence of impostor feelings among women in male-dominated fields is rebuked as nothing more than my misguided attempt to “blame the patriarchy.” Again, you don’t have to like the book. But given their readership, the WSJ reviewer could chosen to point out how female self-confidence factors into the significant investments that Intel, Boeing, Procter & Gamble, Bristol-Myers Squibb, IBM, MIT, Stanford and others have made into academic and corporate efforts to attract, retain, and advance women in STEM fields. Instead executives and administrators from these and other organizations who have invited me to speak were ridiculed as being “gullible.” The impostor syndrome is real, the reasons why it both impacts and holds women back more are complex, and the consequences serious. All the more reason to applaud reasoned voices who report based on fact and not ideology. I hope the WSJ reviewer is among those who read this. Maybe then she’ll get it. Dr. Valerie Young The Secret Thoughts of Successful Women: Why Capable People Suffer from the Impostor Syndrome and How to Thrive in Spite of It malcolmkiske If America is to remain competitive we need the full participation of women in science and engineering. Kudos to Klawe and Harvey Mudd College for having the vision and determination to encourage the female half of our nation’s best and brightest into a field where they are sorely needed. Let’s hope other colleges follow Harvey Mudd’s lead. schmoe >Add to that any assumptions that as a woman or a person of color that you got where you are solely as a result of affirmative action (which in the minds of some translates into the belief that you are automatically less capable) As a (female) student of Harvey Mudd who was admitted before “The Klaw” (as she is colloquially known) made her changes to the admissions process, I am not personally worried by any belief that I graduated through affirmative action. I am, however, concerned that the changes she has made will devalue my degree. The recent female admitted students have SAT and GPA scores that are significantly lower than those in years past. It is not difficult to conclude from this evidence that overall quality of students is indeed being sacrificed. Combined with changes to the core curriculum to reduce the amount of mathematics, and general thinning of requirements, I get the impression that the integrity of the school is being sacrificed. Combined with (newly Klaw-appointed) deans signing off on posters that made for an uncomfortable school environment? I would no longer recommend the college to any upcoming high school students. Go somewhere else instead. Posting semianonymously, since I never bothered to get a forbes account. We are a global women’s network whose mission is to generate exceptional professional and social value for its members. Through regional events and our online, password-protected community, members engage in a rapid, high-powered exchange of ideas and information which is what makes 85 Broads unique. Find out more: www.85broads.com More from 85 Broads Follow 85 Broads on Twitter 85 Broads’ RSS Feed 85 Broads’ Profile 85 Broads’ Website

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Google CEO Larry Page Reveals Surgery Fix For His Hoarse Voice About a year after announcing that he was skipping out on public speaking engagements because he lost his voice and raising concerns over the state of his health, Google Google CEO Larry Page explained the reason he went mum and why his voice continues to sound hoarse: vocal cord nerve strain. Page, offering reassurance that he remains in good health, said he suffered a cold 14 years ago that led to a nerve condition in his left vocal cords. Another cold last summer further damaged his voice, he said in a blog post on his Google+ page today. “Thankfully, after some initial recovery I’m fully able to do all I need to at home and at work, though my voice is softer than before. And giving long monologues is more tedious for me and probably the audience,” Page said in the post. ”Vocal cord nerve issues can also affect your breathing, so my ability to exercise at peak aerobic capacity is somewhat reduced. That said, my friends still think I have way more stamina than them when we go kitesurfing! And Sergey says I’m probably a better CEO because I choose my words more carefully.” Questions about Page’s health emerged last year after he skipped out on several Google events — including the company’s earnings call and its annual Google I/O Developer conference. Page, 40, said today that he will be providing “significant funding” for a program to study voice conditions like his, which he described as “rare.” That project is being led by Dr. Steven Zeitels from the Harvard Medical School and the Massachusetts General Hospital Voice Center, who gained fame after operating on the vocal cords of the singer Adele in 2011. “Though my condition seems to be very rare, there are a significant number of people who develop issues with one vocal nerve,” Page added. Dr. Zeitels is” really excited about the potential to improve vocal cord nerve function.” Page said the cause of his nerve strain was likely a virus, though there’s no way to be certain. His search for the cause led him to be diagnosed in 2003 with a thyroid condition called Hasimoto’s thyroiditis, which causes inflammation and which the Mayo Clinic says affects mostly middle-aged men. “This is a fairly common benign inflammatory condition of the thyroid which causes me no problems,” Page said. “It is unclear if this is a factor in the vocal cord condition, or whether both conditions were triggered by a virus.” From his early days, Page has been considered the quieter of the pair of Google co-founders. Stanford professor and billionaire David Cheriton recalled that Page was “thoughtful and a little more introverted” in an interview with FORBES last year. “If you’d ask me even a few years back, I would have thought Sergey [Brin] would have been the more obvious CEO than Larry,” says Cheriton, who cut a $100,000 check to the Google cofounders in 1998 when they were still Ph.D. students. Coincidentally, Page’s health disclosures came on the same day that actress Angelina Jolie announced that she had a double mastectomy earlier this year to reduce her risk of breast cancer. Like Page, who said he hopes other patients with vocal cord conditions will participate in a survey to help doctors collect more data, Jolie said she decided to detail her “medical choice” in a New York Times post to help raise public awareness about the potential health issues she faced. Here’s Page’s post in its entirety: About 14 years ago, I got a bad cold, and my voice became hoarse. At the time I didn’t think much about it. But my voice never fully recovered. So I went to a doctor and was diagnosed with left vocal cord paralysis. This is a nerve problem that causes your left vocal cord to not move properly. Despite extensive examination, the doctors never identified a cause — though there was speculation of virus-based damage from my cold. It is quite common in cases like these that a definitive cause is not found. While this condition never really affected me — other than having a slightly weaker voice than normal which some people think sounded a little funny — it naturally raised questions in my mind about my second vocal cord. But I was told that sequential paralysis of one vocal cord following another is extremely rare. Fast forward to last summer, when the same pattern repeated itself — a cold followed by a hoarse voice. Once again things didn’t fully improve, so I went in for a check-up and was told that my second vocal cord now had limited movement as well. Again, after a thorough examination, the doctors weren’t able to identify a cause. Thankfully, after some initial recovery I’m fully able to do all I need to at home and at work, though my voice is softer than before. And giving long monologues is more tedious for me and probably the audience. But overall over the last year there has been some improvement with people telling me they think I sound better. Vocal cord nerve issues can also affect your breathing, so my ability to exercise at peak aerobic capacity is somewhat reduced. That said, my friends still think I have way more stamina than them when we go kitesurfing! And Sergey says I’m probably a better CEO because I choose my words more carefully. So surprisingly, overall I am feeling very lucky. Interestingly, while the nerves for your vocal cords take quite different routes through your body, they both pass your thyroid. So in searching for a cause for both nerves that was an obvious place to look. I was diagnosed with Hashimoto’s thyroiditis in 2003. This is a fairly common benign inflammatory condition of the thyroid which causes me no problems. It is unclear if this is a factor in the vocal cord condition, or whether both conditions were triggered by a virus. In this journey I have learned a lot more about voice issues. Though my condition seems to be very rare, there are a significant number of people who develop issues with one vocal nerve. In seeing different specialists, I met one doctor — Dr. Steven Zeitels from the Harvard Medical School and the Massachusetts General Hospital Voice Center — who is really excited about the potential to improve vocal cord nerve function. So I’ve arranged to fund a significant research program through the Voice Health Institute, which he will lead. Thanks a bunch to my amazing wife Lucy, for her companionship through this journey and for helping oversee this project and get it off the ground. Also, thanks to the many people who have helped with advice and information many of whom I have not had a chance to thank yet. Finally, we’ve put together a patient survey to gather information about other people with similar conditions. As it’s fairly rare, there’s little data available today — and the team hopes that with more information they can make faster progress. If you have similar symptoms you can fill it out here: voicehealth.org/ip With additional reporting by Ryan Mac

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Help | Connect | Sign up|Log in Kenneth Rapoza, Contributor I cover Brazil, Russia, India & China. Is China's Ownership Of U.S. Debt A National Security Threat? Is China‘s ownership of nearly $1 trillion in U.S. Treasury debt a threat to our national security? I’ll start with the short answer in case you want to go on to LOL Catz…no, it is not a threat. Such is the assessment of the U.S. China Business Council (USBC), a lobby for U.S. multinationals doing business in China. Oh, you jest, you might say. What do you expect a pro-China lobby to say? Consider this, the U.S. has around $16 trillion in outstanding debt and most of it is held by us, and the bulge bracket banks here at home: Goldman Sachs, JP Morgan, Citibank, Bank of America. Around 7.5 percent is held by China, the biggest foreign holder of U.S. debt. One of the reasons why China has so much Treasury holdings is because of trade. Companies put money in short term Treasury notes and bills to settle trade payments. China’s government could also call all of its own holdings and demand full payment of the money it lent us in principal plus interest, but under what circumstance would they do such a thing? It would be a national security risk if China held a position where they could dictate U.S. policy on fiscal and monetary matters. They cannot. If the economy was crashing and China got terrified and wanted their money back, unless the U.S. defaulted, it would hand it over and there would be nothing China would get in return. Moreover, when the U.S. economy was collapsing in 2008 all the way to the 666 low on March 6 in the S&P 500, China never retreated from Treasurys, or demand Congress get its finances in order or else it would choose to buy euros, or gold instead. The Pentagon did an evaluation on the risks posed by China’s ownership of U.S. debt in July and came to the same conclusion: “Attempting to use U.S. Treasury securities as a coercive tool would have limited effect and likely would do more harm to China than to the United States.” The report was sent to congressional committees by Defense Secretary Leon Panetta, who called China’s ownership of U.S. debt non-problematic and non-threatening. The USBC’s take is that Chinawants its holdings of Treasury debt to gain value, not lose value. And just because interest rates are going down, that doesn’t mean China is losing value on those holdings. Lower interest rates might be bad for income generation, but they mean more demand for bonds, which means higher bond prices. China wants the U.S. economy to prosper because that means China will be able to continue exporting here. As it is, exports from China to the European Union are all down. Exports to the U.S. are up. China is not in a position to threaten the U.S. with financial “terrorism” of any kind. A decision by China to sell off massive positions of U.S. debt would send the American economy into a downward spiral, harming not only the value of China’s investments, but also China’s export-driven economy. The bigger issue for the U.S., says John Frisbie, director of the USBC in Washington is the size of our fiscal deficit and the long term implications for the economy, not the level of China’s debt holdings. USBC’s leadership unveiled their trade agenda for Congress on Tuesday in a report available on their website. “The US-China relationship is fast becoming the most important bilateral relationship for both countries, if it isn’t already,” Frisbie said in a statement on Wednesday. “Its importance is only going to grow. We need to expand our engagement. Importantly, we need to get smarter about China.” Congressmen Charles Boustany (R-LA) and Rick Larsen (D-WA), co-chairs of the Congressional US-China Working Group, each gave brief remarks. “There is much to be gained in both economic and strategic terms if we get the relationship right, but economic and strategic difficulties lie ahead if we do not,” Larsen said. sufiy World Gold Council has now confirmed the Chinese are going to back the yuan with gold. If it is true – to call it The Ground Breaking will be the understatement of the year. Welcome to the Currency Wars at its Prime. Now all recent Japan and China rhetoric about the “territory conflict” will be put in the very dangerous context. Will They dare to make The War to protect the Status Quo for the doomed “Reserve Currency of Choice” – US Dollar? WGC: Gold, the Renminbi and the Multi-currency Reserve System KingWorld News: Massive Squeeze Coming As WGC Confirms Gold-Backed Yuan http://sufiy.blogspot.co.uk/2013/01/world-gold-council-has-now-confirmed.html# Im not an expert on that by any means, but…gut feeling…I find that hard to believe. lcr1946 Well it’s good to see somebody standing up to explain to all those who’ve learned their economics from their Representative that China nor anyone else is going to own us. China dosent own the USA but it for sure can do damage… just like the Japanese… if the Japanese started to dump their 800 trillion is US government bonds… others will follow suit… including around 10 trillion in US debt held directly or indirectly by the American people… being a contrarian trader I have seen people dump in total panic and fear, and people pull their bids… knowing it would be foolish to buy when they know the security is going south… individual investors, fund managers, pension fund managers etc etc etc are all human… they did not invest to prop up the US economy… they invested to make money… when the bonds markets turn south… these investors will not be thinking lets hold on and support the USA they are thinking lets sell at a loss before I lose it all… Click on the link to the Bloomberg story about the Pentagon report. They said that it was unlikely and would cause “some” damage but that it would be “minimal” if — in the rare case — China (or Japan, or both) opted to call their bonds. well Ill agree… the US Federal Reserve purchased 61% of the Treasury debt issued by the US Treasury in 2011 using money they printed out of thin air… with all the Quantitative Easing they have been doing over the last 5 years… im sure the Pentagon thinks they can just buy up that debt as the Chinese dump it… and your right they dont want to rock the boat with the USA… this is money they have made from their export surplus anyways but if China wanted to hit the secondary bond markets with its selling it will drop the market… temporarily or not… I view it as more than temporary as the too big to fail Western Banks…have up to 1.5 “Quadrillion” (at least 600 trillion) in derivatives bets where they can only 2 to 4% of those bets any move in the market temporary or not they will not be able to cover the margin calls on these loses as their futures markets get slammed… really I only see the Chinese using this as a weapon… to distract the USA in a brief territorial skirmish with Japan or more likely the Philippines *correction* Western Banks…have up to 1.5 “Quadrillion” (at least 600 trillion) in derivatives bets where they can only cover 2% to 4% of those bets Dunno, David. That’s insider baseball, anyway, not something us mere mortals outside TSY and the Pentagon will know. At least not til years later when someone writes a book: “We would have said this or did that in favor of Japan but China threatened this and that and the White House backed down.” Until then…we got nothing. Craziness. I know. Assets securitized by other assets securitized by the securitization….Bain & Company report released in Nov. talks about this and says we have to learn to live with bubbles created by this superabundance of capital. well we do have precedence…it was said the reason the US government rescued Fannie Mae and Freddie Mac… way back at the height of the 2008 was because foreign bond holders of their long term debt, demanded the US government make good on their debt… . . The top five foreign holders of Freddie and Fannie long-term debt are China, Japan, the Cayman Islands, Luxembourg, and Belgium. In total foreign investors hold over $1.3 trillion in these agency bonds, according to the U.S. Treasury’s most recent “Report on Foreign Portfolio Holdings of U.S. Securities.” FreedomWorks President Matt Kibbe commented, “The prospectus for every GSE bond clearly states that it is not backed by the United States government. That’s why investors holding agency bonds already receive a significant risk premium over Treasuries.” “A bailout at this stage would be the worst possible outcome for American taxpayers and mortgage holders, who have been paying a risk premium to these foreign investors. It would change the rules of the game retroactively and would directly subsidize the risks taken by sophisticated foreign investors.” “A bailout of GSE bondholders would be perhaps the greatest taxpayer rip-off in American history. It is bad economics and you can be sure it is terrible politics.” Reuters article Kenneth Rapoza I've written about Brazil pre-Lula and post-Lula and spent the last five years covering all aspects of the country for Dow Jones, Wall Street Journal and Barron's. Meanwhile, for an undetermined amount of time, and with a little help from my friends, I will be parachuting into Russia, India and China. (I figure if Anderson Cooper can parachute, I can parachute.) More from Kenneth Rapoza Follow Kenneth Rapoza on Twitter Kenneth Rapoza’s RSS Feed Kenneth Rapoza’s Profile

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Australians make debut with Minardi Australians make debut with Minardi 24 Nov 2004 The second day of Minardi's week-long Misano test session had a distinctly Antipodean feel, as young Australian drivers, Will Davison and Will Power, both experiencing Formula One performance for the first time, joined Israeli driver Chanoch Nissany, who was completing a two-day programme with the team.Once again, the primary objective of the day's activities was to provide the drivers with the chance to acclimatise to Formula One power, although the team's engineers also took the opportunity to evaluate some new aerodynamic components, which may be used in 2005. Power and Davison, rivals in this year’s British Formula Three championship, both completed 22 laps of the Italian circuit, with Power just edging it in the times with a 1m 11.790s to Davison’s 1m 11.900s."It was very, very impressive, like nothing else I've ever driven,” said Power. “You just can't describe the brakes and the power, but ultimately, it's just another car, and you have to get used to it and become physically fit enough to drive race distances in it if you're going to do F1. “The track proved to be quite easy to learn - it's mostly slow and medium-speed corners, and other than the left-handers going onto the back straight, which are taken 'flat', there are no massively quick corners. Once I'd familiarised myself with the layout, I just found the quicker I went, the more I loved it. It was huge fun!"Davison was equally enthusiastic, commenting: "That was just an awesome experience - incredible! You can prepare physically as much as you like, but nothing can really prepare you for the experience of driving a Formula One car for the first time. The power is amazing, although you do start to adapt to it quite quickly, but the whole package - the engine, the gears, the brakes - is just perfect. In fact, there is so much grip in the car, and the brakes are so good, that it's difficult to find the limit of the car in a short space of time, but at a test like this, that is exactly what you need to do. “Personally, I feel pretty happy with the job I did today. I didn't make any mistakes, and each time I went out, I found there was something new to learn. I particularly want to thank Paul Stoddart, the engineers, and the whole Minardi team, all of whom have made me feel extremely welcome. That, in turn, hat has made my job easier. The problem is, now I've had a small taste of F1, I want more, because I definitely felt as though I was capable of doing a good job on the basis of today's experience."As the two Australians revelled in their first Formula One experience, Nissany continued with development work, clocking up 50 laps with a best time of 1m 14.000s."Today was very different for me in terms of the morning and afternoon sessions,” he reported. “In the morning, the car was in 2004 specification, but in the afternoon, I had the honour to be the first person to drive a Minardi with 2005 aerodynamic package. It is immediately clear that there is much less downforce available, and I believe this cars will be much more difficult to drive and will demand considerable skill from the driver. Overall, I felt things went well today, and I would very much like to have the opportunity to continue my F1 ‘learning curve’ with the team."Team boss Paul Stoddart summed up Minardi’s day, saying: "All three drivers today put in a solid performance but I was particularly pleased to be able to fulfil a promise made twelve months ago to give two young Australian drivers, Will Power and Will Davison, the opportunity to realise the dream of a lifetime, by driving an F1 car. “They both acquitted themselves with distinction, in that they were on the pace quickly and set very competitive times after only a relatively small number of laps. This is hugely significant, when you consider neither of them had ever sat in an F1 car before today. I believe both have a positive future and let's hope at least one of them is able to follow in Mark Webber's footsteps. “Chanoch had a difficult job, having been selected to test the interim, 2005 specification aerodynamics. He quickly realised the significance of the massive reduction in downforce, and provided the team with some useful feedback on its 2005 aero package."On Wednesday at Misano, the emphasis switches to Minardi’s F1 two-seater programme, as Zsolt Baumgartner, Christijan Albers and Nicolas Kiesa spend the day providing high-speed chauffeur services to nearly 50 passengers.

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Liuzzi steps up to race for Force India Liuzzi steps up to race for Force India 07 Sep 2009 Force India have announced that test driver Vitantonio Liuzzi will assume driving duties of car number 21 from this weekend's Italian Grand Prix, taking over from Giancarlo Fisichella who has moved to Ferrari.After evaluating options following Fisichella's switch, Liuzzi has been promoted to the race seat from Monza onwards. The 28-year-old Italian has fulfilled the team's test, reserve driver and development role from the start of the 2008 season.“I can't wait to get back into the car in race trim, particularly at my home Grand Prix in Monza,” said Liuzzi. “I really appreciate the opportunity (team owner) Vijay (Mallya) has given me, particularly now Force India has a great car that's performing very well. I am confident I can carry on our progress.“I'm very motivated, I'm in good shape and hungry to get some more points on the board. Although it's unfortunate that this came about as an direct result of Felipe's (Massa’s) accident, this is my opportunity to show people what I can do and I'm really looking forward to it.”Liuzzi has 39 Grand Prix starts to his name, having previously competed for Red Bull Racing in 2005 and then for Toro Rosso in 2006 and 2007. His best finish was a sixth place at the 2007 Chinese Grand Prix.Mallya commented: “I'm delighted to give Tonio the opportunity to get back into a race seat, which I know he has been itching to do for the past two years. Force India is now in a very competitive position and we need a driver who can continue this momentum. This will be the chance for Tonio to demonstrate to both the team and the field that he has the commitment, speed and professionalism to perform and I am sure he will seize this opportunity.” Fisichella to race for Ferrari at Monza, reserve role for 2010

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County Home > Public Health > Preventive Health Debbie Mason January 2014 marks the 50th anniversary of the first Surgeon General’s Report on Smoking and Health. The report highlights 50 years of progress in tobacco prevention and control, presents new data on the health consequences of smoking, and discusses opportunities to potentially end the smoking epidemic in the United States. Read the fact sheet and access the full/executive reports.

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Follow Jesus Teaching Others to Walk: The Use of Creeds and Confessions In Local Church Reformation Only be careful, and watch yourselves closely so that you do not forget the things your eyes have seen or let them slip from your heart as long as you live. Teach them to your children and to their children after them. Deut 4:9 The Future Generation God is concerned about the future generations. Psalm 78:1-6 says: O my people, hear my teaching; listen to the words of my mouth. I will open my mouth in parables, I will utter hidden things, things from of old � what we have heard and known, what our fathers have told us. We will not hide them from their children; we will tell the next generation the praiseworthy deeds of the LORD, his power, and the wonders he has done. He decreed statutes for Jacob and established the law in Israel, which he commanded our forefathers to teach their children, so the next generation would know them, even the children yet to be born, and they in turn would tell their children. (NIV) Psalm 145:4 similarly says: "One generation shall praise thy works to another, and shall declare thy mighty acts" (KJV). One of the best teaching tools available in a reforming situation is the use of creeds, confessions and catechisms. Unfortunately, the use of these teaching tools has been lost in all-too many churches. Yet it is vitally important that we recover the use of our historical confessional statements. Reformation will not come if we do not know who we are and where we have come from. To this end, in my view, every reforming pastor should have on his shelf and in his church library a copy of Timothy and Denise George�s collection of Baptist confessions of faith, covenants and catechisms. Definition Of Creeds, Confessions and Catechisms It is often said that Baptists are not creedal people, that we have no creed but the Bible. This simply is not true. Baptists have often utilized confessions of faith, beginning with the General Baptists� Short Confession of Faith in Twenty Articles (1609) and the Particular Baptists� London Confession of 1644 and continuing to the Southern Baptist Convention�s Baptist Faith and Message, recently amended in 1998. We had better have some agreement as to the definitions of a "creed" and "confession." The word "creed" comes from the Latin word credo, and it simply means "I believe." Thus, when we say we believe certain things about Bible truth, we are saying we have a creed. A "confession of faith" is simply a declaration of those things believed by us. More specifically, it is a declaration of the manner in which a person, a number of people, or a church understands the truth revealed in the Bible. A "catechism" is a statement of faith presented in the form of questions and answers, in a way that even children can understand. It is important to have an inerrant Bible, but what good is an inerrant Bible if we do not know what it teaches or how to apply it to everyday practice? Many heretics and cults believe the Bible. However, it is their interpretation as to what the Bible teaches that has led them to their cultic and heretical views. Creeds and confessions come into existence to combat error. Invariably, they are born of controversy concerning what the Bible teaches in some respect. The Scriptures are from God, but the understanding of them belongs to the part of man. To the best of their ability, and with the aid of the Holy Spirit, men must interpret each particular part of Scripture separately, and then combine all that the Scriptures teach upon every subject into a consistent whole, and then adjust their teaching upon different subjects in mutual consistency as parts of a harmonious system. When you do this, you have a creed or confession of faith founded on Scripture alone. Behind every creed and confession is Pilate's question, "What is truth?" What is the truth of God? The Confessions seek to answer that question assuming the truth is in the Bible and by appealing to the Bible as the only authoritative source of truth. When you ask a man the question, "What do you understand the Bible to teach?" and he answers you with a series of texts, he would be telling you nothing, unless at the same time he would state what he understands those texts to mean. When he proceeds to say what he believes these texts to mean he is giving you his creed and confession of faith. It may sound quite pious to say, "I have no creed but Christ, and no textbook but the Bible," but which Christ are you talking about? There are a thousand Christs on the religious market, but they are not all the Christ of the Bible. It is likewise with the statement "The Bible is my textbook." Most religious crackpots or cultists would make the same claim. Therefore, someone must articulate what the "textbook" teaches or means, and how it applies to faith and practice. This is why the great creeds came on the historic scene. The Westminster Confession of Faith and the First and Second London Baptist Confessions of Faith refute the heresies of Arianism, Socinianism, Gnosticism, Pelagianism, Semi-Pelagianism, Universalism, Arminianism and Antinomianism without even mentioning them by name. A creed or confession of faith is not the voice of divine truth, but the echo of that voice from men who have heard the utterance of divine truth, men who have felt the power of divine truth, and who have answered the call of divine truth. Do Baptists Have Creeds Or Confessions?

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Campaign to save Thanksgiving Not everyone is excited about Black Friday extending into the Thanksgiving holiday. LITTLE ROCK, AR - Not everyone is excited about Black Friday extending into the Thanksgiving holiday. Many retail workers are speaking out through social media in an effort to save Thanksgiving from turning into a national shopping day.Shoppers no longer have to set their alarms to wake up early. Best Buy, Target, Kohl's, and Macy's will open their doors at midnight instead of the traditional 5am on Black Friday in an effort to encourage more shoppers to spend more money.Moving Black Friday to Thanksgiving Day disappoints nearly 93,000 retail workers who signed a petition that encourages people to spend time with their families and not at the store. But retailers say it's what their customers want.Jane Wayland is the Chair of the Marketing and Advertising Department at UALR. She says if shoppers didn't want to shop, then retailers wouldn't open early. "They have to pay workers and it costs them to keep the stores open, so if it wasn't profitable they wouldn't do it." 212 million shoppers spent nearly $400 per person last year on Black Friday. 60 percent finished shopping before 9am. Andy Gallowa is the store manager at Target on Chenal Parkway in Little Rock. He says opening earlier is what customers have been asking for. "Our guests really want to shop after their Thanksgiving dinner rather than get up in the middle of the night."Joyce Yuratich plans to shop on Black Friday. "I like the idea." So does Del Mika. "After turkey, I'm going to be headed out of the house." What about the workers? Target corporate headquarters says, "Target does our best to work around the schedules of all of our team members, making every effort to accommodate their requests. Target will offer holiday pay to all hourly team members who work on Thanksgiving."Wayland says if people don't like the retailers cutting into Thanksgiving Day, then they don't have to shop. "To stop it, don't go to the store. You shop with your feet. If you want to make an impact, don't spend the money."Sears and JC Penney will not open on Thanksgiving Day so workers can be with their families. In just the last two days, the number of people who have signed the petition to save Thanksgiving has grown from 7,000 people to more than 93,000 people. Copyright 2011 Newport Television LLC All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

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Detmer, Johnson, Fulmer enshrined in HOF Atlanta, GA (Sports Network) - Heisman Trophy winner Ty Detmer of BYU and national championship coaches Jimmy Johnson and Phillip Fulmer were enshrined into the College Football Hall of Fame on Wednesday.A total of 14 players and three coaches from the Football Bowl Subdivision (formerly I-A) were selected for enshrinement.Joining Detmer among players are quarterbacks Steve Bartkowski from California and Tommy Kramer of Rice, running backs Charles Alexander of LSU, Otis Armstrong from Purdue, wide receiver Art Monk of Syracuse, Notre Dame tight end Dave Casper, offensive linemen Jonathan Ogden of UCLA and John Wooten of Colorado, split end Hal Bedsole of Southern California, defensive tackle Gabe Rivera of Texas Tech, Kansas State linebacker Mark Simoneau and defensive backs Greg Myers of Colorado State and Scott Thomas of Air Force.Johnson, who coached at Miami-Florida and Oklahoma State, and Tennessee's Fulmer will be joined by Texas A&M's R.C. Slocum as coaches in this year's class.Detmer won the 1990 Heisman Trophy and was twice a consensus All-American from 1988-91 at BYU. He finished his career with 15,031 passing yards and 121 touchdowns -- both NCAA bests at the time -- and still holds nine NCAA records.The sixth Cougar inducted into the Hall, Detmer helped BYU to three conference championships and a record of 37-13-2. He went on to play 14 seasons in the NFL with the Packers, Eagles, 49ers, Browns, Lions and Falcons.Johnson spent five seasons as head coach at Oklahoma State, then went on to a highly-successful five-year run at Miami-Florida. The Hurricanes were 52-9 under Johnson with five New Year's Day bowl appearances, and his 1987 squad won the national championship with a 20-14 victory over Oklahoma in the 1988 Orange Bowl.A member of Arkansas' national championship team as a player in 1964, he posted an overall collegiate record of 81-34-3 from 1979-88. He left for the NFL in 1989 and guided the Dallas Cowboys to a pair of Super Bowl titles. In addition to his five-year stint with Dallas, Johnson also coached the Miami Dolphins from 1996-99.Fulmer was the head coach at Tennessee from 1992-2008, a 17-year tenure highlighted by the school's sixth national championship in 1998. He led the Volunteers to a record of 152-52 with 15 bowl appearances and a pair of SEC titles.Bartkowski is the 16th Cal player selected for the Hall of Fame. He led the nation in passing with 2,580 yards in his senior year of 1974 and was then the first pick of the 1975 NFL Draft. Bartkowski was the league's top rookie with the Falcons and played 11 seasons with Atlanta and one year with the Rams.Kramer was fifth in the Heisman Trophy voting during his senior season of 1976 at Rice when he led the nation with 3,317 passing yards and 3,272 yards of total offense while earning Southwest Conference Player of the Year honors. He was a first-round pick by the Vikings in the 1977 draft and played 14 years in the NFL.Alexander, the eighth LSU player inducted into the Hall, left LSU after the 1978 season as the SEC's all-time leader in rushing attempts, yards and touchdowns. He ran for 1,172 yards and 14 touchdowns in his senior season of 1978 and went on to a seven-year pro career with the Cincinnati Bengals.Armstrong was the Big Ten MVP as a senior at Purdue in 1972 and was eighth in that year's Heisman Trophy balloting. His 3,315 career rushing yards set school and conference records at the time. He was a first-round pick of the Denver Broncos in 1973, led the NFL in rushing in 1974 and helped the franchise to its first Super Bowl after the 1977 season.Monk, a Pro Football Hall of Fame inductee in 2008, was the top player in the East as a freshman in 1976 and again as a senior in 1979. He led Syracuse in receiving for three straight seasons and helped the school to its first bowl win in 13 years with a 31-7 victory over McNeese State in the 1979 Independence Bowl. A first-round pick of Washington in 1980, Monk spent 14 seasons with the Redskins, winning three Super Bowl titles, and one year with the Jets.Casper, the 44th Notre Dame player chosen for the Hall, was the Irish's offensive MVP during his senior season of 1973 when he led the school to a national championship. He went on to play 11 seasons in the NFL with Oakland, Houston and Minnesota, earning four Pro Bowl berths, a Super Bowl title with the Raiders and selection to the Pro Football Hall of Fame in 2002.Ogden, the 1995 Outland Trophy winner and a unanimous All-American in his senior year, is the 11th UCLA member of the Hall of Fame. He was a four-year starter at left tackle, then played 12 seasons with the Baltimore Ravens. An 11-time Pro Bowl selection, he helped Baltimore to the Super Bowl title after the 2000 season.Wooten, selected by the veterans' committee, was a 1958 All-American at Colorado. The Buffaloes had one of the nation's top rushing attacks during his three seasons, during which the school was 20-9-2 and beat Clemson in the 1957 Orange Bowl. He played 10 seasons in the NFL with Cleveland and Washington.Bedsole helped USC to the 1962 national championship and is the 30th Trojan to enter the Hall. He caught 33 passes for 827 yards with 11 touchdowns during an All-America senior season of '62, capping the record-setting year with a pair of TD catches in the 1963 Rose Bowl win over Wisconsin.Rivera, nicknamed Senor Sack, averaged 80 tackles per season from 1979-82 at Texas Tech and was a consensus All-American his senior year when he compiled 62 solo stops, 43 assists, 10 tackles for loss and five sacks. After being chosen with the 21st pick in the 1983 draft, his promising NFL career with the Pittsburgh Steelers was cut short in his rookie year by a car accident that left him a paraplegic.Simoneau was a two-time All-America during his career from 1996-99 at Kansas State and holds the school record with 251 career unassisted tackles. He was the 1999 Big 12 Defensive Player of the Year and helped the Wildcats to a record of 42-7 before going on to an 11-year NFL career with Atlanta, Philadelphia, New Orleans and Kansas City.Myers was the 1995 Jim Thorpe Award winner as the nation's top defensive back and was a four-time All-WAC selection. He was also a three-time All-WAC pick as a return specialist.Thomas notched 221 career tackles with 10 interceptions while averaging 28.8 yards per kickoff return from 1982-85 at Air Force. He helped the Falcons to their first WAC title during his senior season as well as a record of 7-1 against Army and Navy with three Commander-in-Chief trophies.Slocum led Texas A&M to a record of 123-47-2 from 1989-2002 and is the winningest coach in Aggie history. His teams produced a Southwest Conference record of 28-0-1 from 1991-94 and three titles. He also led the Aggies to 11 bowl games, including five New Year's Day appearances.

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Franchise Business Opportunities - IFA is the source for all franchise information and resources for business franchises. Printer-friendly version New Health Care Law Places Burden on Backs of Small Business For immediate releaseContact: Alisa Harrison, 202-628-8000aharrison@franchise.orgwww.twitter.com/franchising411 WASHINGTON, May 27, 2010—New healthcare regulations will slow or stall growth of small and mid-sized businesses as they struggle to absorb the new costs, the International Franchise Association warned Congress today. Speaking before the House Republican Health Care Solutions Group forum on the true cost of the new health care law to families and employers, IFA member Gail Johnson, president & CEO of Rainbow Station, Inc., told lawmakers that the new law contains a framework that will encourage further shifting of health costs onto the backs of small franchise businesses. “As an entrepreneur and a nurse, when I review the new health care law I see a structure designed to discourage economic growth among small and mid-sized companies,” Johnson said. “At a time when our government should be doing everything in its power to encourage job growth and recovery, I see a federal requirement that creates disincentives for higher wages, new hiring and robust employee benefits. This law will force me to devote more of our capital investment resources toward operating costs rather than growth.” Johnson said the new law will add costs and regulatory burdens for small business owners, noting the employer mandates will require her company to offer insurance, but much of the flexibility for the plan design will be regulated from Washington. “This inflexible, one-size-fits-all approach betrays a bias toward mandating coverage rather than curbing costs,” Johnson said, observing that the law creates a strong disincentive to hire new employees, especially as firms reach the threshold level of 50 full-time workers. “This represents a significant government intrusion into the benefits decisions of employers. In order to comply, small employers will be faced with decisions such as cutting back wages, forgoing new hiring and raising prices for services. These measures will further stunt any economic recovery and curtail future job growth.” “At Rainbow Station, we currently pay 75 percent of health insurance coverage to full-time employees but do not offer coverage to spouses or family members. The new provision will drive health insurance costs higher than we are able to provide today,” she added. The company would also have to be mindful that employee’s share of the plan does not exceed 9.5 percent of their household income. Otherwise, they would be eligible for subsidies and would trigger penalties of up to $3,000 per employee who receives a subsidy. “How are employers supposed to determine the household income of each employee?” she asked. This is private information that employees would certainly not expect their employers to ascertain in most cases. “The federal government has now forced the hands of small and mid-sized businesses and made health insurance an obligation, rather than a benefit of employment that I could use to supplement salary and wages in order to attract and retain quality staff,” Johnson said. “Essentially, the decision to offer health insurance coverage will strictly be about cost—insurance premiums versus penalties. Health insurance coverage will cease being a benefit of employment or part of a competitive compensation package.” “For a growing company like ours, which provides an important service to the community, the thresholds for the tax credit are entirely too small to be of any assistance,” Johnson said. “In order to qualify for the tax credit, we would have to cut hours for our full-time staff to ensure we were under the 25 full-time equivalent employee threshold. Staffing in the childcare industry requires mandated ratios of staff to children. We simply could not take advantage of any tax credits to offset insurance costs. Encouraging companies to cut back hours or eliminate staff is the wrong message our government should be sending small businesses - particularly during a recession.” Franchised businesses play an important role in the economic health of the U.S. economy, and they are poised to help lead the economy on the path to recovery. IFA Educational Foundation reports show that the franchise businesses provide over 20 million jobs and contribute $2.3 trillion to the U.S. economy. Rainbow Station, Inc. is a nationally accredited preschool and school age recreation franchise that offer backup childcare for mildly ill children on site, which provides developmentally appropriate early education and school-age recreation to 325 children. There are six corporately owned Rainbow Station programs in Richmond and franchises in Virginia, North Carolina and Texas. All Rainbow Station schools are accredited by the National Academy of Early Childhood Programs and/or the National Afterschool Association’s Council on Accreditation as soon as they become eligible for accreditation. Some schools are accredited by the Southern Association of Colleges & Schools. The Rainbow Station system employs 225 employees – at least 50 per location. Currently, there are nine schools open, with a capacity for 3,131 children. Fully enrolled, each campus will generate $2.5 – $3.5 million in revenue annually, depending on geographic location. Within Rainbow Station facilities, there is the capacity to provide backup care for mildly ill children. This care is overseen by a pediatric nurse and results in approximately 1,000 productive workdays returned to parents who have the option to leave their child with a nurse and go to work. Rainbow Station provides real flexibility and options to working parents who would normally be forced to miss work in order to stay home with a mildly ill child. To read a copy of Gail Johnson’s statement, click here About the International Franchise AssociationThe International Franchise Association is the world’s oldest and largest organization representing franchising worldwide. Celebrating 50 years of excellence, education and advocacy, IFA protects, enhances and promotes franchising through government relations, public relations and educational programs. Through its awareness campaign highlighting the theme, Franchising: Building Local Businesses, One Opportunity at a Time, IFA promotes the 21 million jobs and $2.3 trillion of economic activity generated by franchising. IFA members include franchise companies in over 90 different business format categories, individual franchisees and companies that support the industry in marketing, law and business development POPULAR FRANCHISE LINKS

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SPECIAL TOPIC: THE NEED TO PERSEVERE The biblical doctrines related to the Christian life are difficult to explain because they are presented in typically eastern dialectical pairs (see Special Topic: Eastern Literature [biblical paradoxes]). These pairs seem contradictory, yet both are biblical. Western Christians have tended to choose one truth and ignore or depreciate the opposite truth. Let me illustrate. A. Is salvation an initial decision to trust Christ or a lifetime commitment to discipleship? B. Is salvation an election by means of grace from a sovereign God or mankind's believing and repentant response to a divine offer? C. Is salvation, once received, impossible to lose, or is there a need for continual diligence? The issue of perseverance has been contentious throughout church history. The problem begins with apparently conflicting passages of the NT: A. texts on assurance 1. statements of Jesus (John 6:37; 10:28-29) 2. statements of Paul (Rom. 8:35-39; Eph. 1:13; 2:5,8-9; Phil. 1:6; 2:13; 2 Thess. 3:3; 2 Tim. 1:12; 4:18) 3. statements of Peter ( 1 Pet. 1:4-5) B. texts on the need for perseverance 1. statements of Jesus (Matt. 10:22; 13:1-9,24-30; 24:13; Mark 13:13; John 8:31; 15:4-10; Rev. 2:7,17,26; 3:5,12,21) 2. statements of Paul (Rom. 11:22; 1 Cor. 15:2; 2 Cor. 13:5; Gal. 1:6; 3:4; 5:4; 6:9; Phil. 2:12; 3:18-20; Col. 1:23; 2 Tim. 3:2) 3. statements of the author of Hebrews (2:1; 3:6,14; 4:14; 6:11) 4. statements of John (1 John 2:6; 2 John 9) 5. statement of the Father (Rev. 21:7) Biblical salvation issues from the love, mercy, and grace of a sovereign Triune God. No human can be saved without the initiation of the Spirit (cf. John 6:44,65). Deity comes first and sets the agenda, but demands that humans must respond in faith and repentance, both initially and continually. God works with mankind in a covenant relationship. There are privileges and responsibilities! Salvation is offered to all humans. Jesus' death dealt with the fallen creation's sin problem. God has provided a way and wants all those made in His image to respond to His love and provision in Jesus. If you would like to read more on this subject from a non-Calvinistic perspective, see 1. Dale Moody, The Word of Truth, Eerdmans, 1981 (pp. 348-365) 2. Howard Marshall, Kept by the Power of God, Bethany Fellowship, 1969 3. Robert Shank, Life in the Son, Westcott, 1961 The Bible is addressing two different problems in this area: (1) taking assurance as a license to live fruitless, selfish lives and (2) encouraging those who struggle with ministry and personal sin. The problem is that the wrong groups are taking the wrong message and building theological systems on limited biblical passages. Some Christians desperately need the message of assurance, while others need the stern warnings! Which group are you in? Copyright © 2013 Bible Lessons International

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Jud Heathcote will miss festivities at MSU after fall Michigan State University basketball coach Jud Heathcote, shown in 1995. The question was simple, and the answer was direct. How are you doing, Jud? "Kinda crappy," responded Jud Heathcote, the 85-year-old former basketball coach at Michigan State University and one of the planned guests of honor for this weekend's festivities at Jenison Field House. Heathcote had just called MSU and canceled because of a slip on ice and hard fall to the pavement while going to church with his wife, Beverly, on Sunday in Spokane, Wash. Both of them fell, but he took the fall harder. "I've got a lot of bruises and a lot of pain around my replaced hip," he said. "There's no way I'll be ... Heathcote had just called MSU and canceled because of a slip on ice and hard fall to the pavement while going to church with his wife, Beverly, on Sunday in Spokane, Wash. Both of them fell, but Jud A link to this page will be included in your message.

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Strategies for Getting Things Done in 2013 Last week I discovered two new-to-me strategies for getting things done. Put One Fun Thing On Every To-Do List This came from the description of a to-do app for iOS that I was trying. I decided not to write about the app because it wasn't that great, but the description of it inspired me to start putting one fun thing on my to-do lists. The idea here is that my to-do list won't be just a list of chores. I'll also have some incentive to get the chores done quickly so that I have time for my fun thing(s). Write an Accomplished List This idea came from a notepad that I found in my room at a Marriott hotel. Writing the list of things that I accomplished in the day is a lot more fun than just crossing items off of a list. I'm even listing simple things like "read one chapter in my new book." And I'm including my "fun thing" on my accomplished list too. Bonus: Make a "fun" New Year's Resolution This is a variation on an idea that Norm MacDonald (yes, the Canadian comedian) shared in a Grantland article. We tend to think of New Year's resolutions in terms of things that are difficult to change. What if we had a fun corollary to each difficult resolution? When you do one, do the other too. (Of course, I'm talking about fun resolutions that aren't bad for you. Norm MacDonald wasn't using it the same way in the article of his that I read which is why I didn't directly link to it). at Getting Things Done, New Year's Resolution, Use Wolfram Alpha to Create a Strong Password Handy New Diigo Browser Extension Features

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:: French Links :: Italian Links Home :: Resources French Interdisciplinary Group | Norman B. Spector Scholars Fund | Paris Program in Critical Theory | MMLC French Interdisciplinary Group The French Interdisciplinary Group (FIG), founded in 1996, is one of a dozen interdisciplinary centers (or "centres d'excellence") in the US supported by the French government. Over 50 faculty members in the Humanities, Social Sciences, Sciences, and the professional schools, and a similar number of graduate students are affiliated with the group. FIG supports presentations, seminars, and colloquia on French or francophone studies, on French scholarship, and presentations by French visitors in all disciplines. It offers two regular speakers’ series, the Causeries, for undergraduates, and the Cafés Philosophiques, organized by and for graduate students. Fig supports graduate studies as well. It provides small summer grants, actively collaborates with the Paris Program on Critical Theory and the dual PhD Program in International and Intercultural Studies in partnership with the Institut d’Études Politiques de Paris (Sciences Po). It is actively involved in the management and development of graduate exchange programs with the École Normale Supérieure, rue d’Ulm and the École Normale Supérieure, Lyon. FIG works to form new partnerships and programs with French institutions of higher education, notably Sciences Po, the École des Hautes Études en Sciences Sociales (EHESS), and, for the natural sciences, the Université Louis Pasteur of Strasbourg. In this regard, FIG works closely with the Office for International Program Development. It also oversees regular faculty exchanges with Sciences Po and EHESS. For Upcoming Events and more information on all aspects of our endeavors consult our webpage or contact one of the co-directors: Nasrin Qader, Associate Professor of French 491-8263 n-qader@northwestern.edu Michael Loriaux, Associate Professor of Political Science m-loriaux@northwestern.edu Center for International and Comparative Studies Norman B. Spector Scholars Fund The Norman Spector Scholars' Fund honors the memory of our late colleague, the chair of the department for the first decade after its founding and an unforgettable teacher and friend. In 2003-04 the Spector Fund helped bring Leo Bersani , of the University of California-Berkeley, to teach two courses in the Spring quarter and to deliver the first series of three Spector Lectures, which will continue in the future. In addition the Fund covers the student Essay Prizes awarded each spring, as well as student travel (for the French Government Youth and Sports Grants and for the Grande Dictée des Amériques in Québec each year). Paris Program in Critical Theory The Northwestern University Paris Program in Critical Theory, inaugurated in Fall of 2001, affords advanced graduate students from a wide variety of disciplines a unique opportunity to familiarize themselves with French and European theoretical research by spending one year in Paris under optimal conditions. The Paris program, directed by Samuel Weber, Avalon Professor of the Humanities at Northwestern University, has two major functions: to provide funding for a one year stay in Paris and to create a situation in which that year can be put to best possible use. The Paris Program provides a full fellowship support for one year to up to five highly qualified graduate students from Northwestern. In the Fall quarter, these students participate in a weekly interdisciplinary seminar organized by the Program's Director, Professor Weber. The Director also assists students in making contact with leading European scholars and researchers in their respective fields. Students spend the rest of the year in study and/or research according to their individual projects. For further information on this program, see the Paris Program site. Multimedia Learning Center The Multimedia Learning Center (MMLC,) is directed by Katrin Völkner of the Department of German. The MMLC provides a wide range of instructional support services to all language departments including the standard language laboratory services. In addition, the Center collaborates with instructors to develop innovative courseware and class projects, including such well-received and popular projects as Creative Writing in Italian, Internautique, Internef, Italian Soap Operas, and the Picpus Digital Archive. Additional information on MMLC services can be found at: http://mmlc.northwestern.edu Home | Graduate | Undergraduate | Placement | Study Abroad | Courses | People | Events | Resources WCAS Home | Northwestern Home | Northwestern Calendar: Plan-It Purple Northwestern Search Department of French and Italian Weinberg College of Arts and Sciences 1880 Campus Drive Kresge Hall 2-375 Evanston, Illinois 60208-2204 Phone (847) 491-5490 Fax (847) 491-3877 E-mail french-italian@northwestern.edu Last Updated:07/30/2013 World Wide Web Disclaimer and University Policy Statements � 2007 Northwestern University.

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VisitMuseum Director's Greeting CollectionSearch the Collection Areas of the Collection Works on View Special Loans ProgramsBrowse Programs Courses and Conversations Group and School Visits Studio Programs Photoarchive Center for Collecting Museum Research Research Staff Profiles InteractVideo SupportMembership Corporate and Private Entertaining ShopBooks and Catalogues Museum Inspired Gifts Exhibition Banners About | Calendar | Tickets | Careers | Press | Join Home › Exhibitions › Past › Visit Past Exhibitions 2014| Vermeer, Rembrandt, and Hals: Masterpieces of Dutch Painting from the Mauritshuis October 22, 2013 to January 19, 2014 The Frick Collection was the final American venue of a global tour of paintings from the Royal Picture Gallery Mauritshuis in The Hague, the Netherlands. Order Catalogue David d'Angers: Making the Modern Monument September 17, 2013 to December 8, 2013 Lauded by Victor Hugo as the Michelangelo of Paris, French sculptor Pierre-Jean David d’Angers (1788–1856) produced many of the most iconic portraits and ambitious public monuments of the Romantic era. An experimental writer, outspoken Republican, and teacher to some of the greatest sculptors of the nineteenth century, David d’Angers cultivated friendships with an array of contemporary artists, writers, scientists, and politicians — from Honoré de Balzac and Niccolò Paganini to Johann Wolfgang von Goethe and Eugène Delacroix. This exhibition included forty-eight works by David on paper and in wax, terracotta, marble, bronze, and plaster, as well as rare nineteenth-century reproductions of his work in photographs and engravings. Order Catalogue The Impressionist Line from Degas to Toulouse-Lautrec: Drawings and Prints from the Clark March 12, 2013 to June 16, 2013 This exhibition presented a selection of nineteenth-century French drawings and prints from the Sterling and Francine Clark Art Institute in Williamstown, Massachusetts. Sheets by Millet, Courbet, Degas, Manet, Pissarro, Gauguin, Toulouse-Lautrec, and other masters are on view. Ranging widely in subject matter and technique and spanning the entire second half of the nineteenth century, these works represent the diverse interests of Realist, Impressionist, and Post-Impressionist artists in a rapidly changing world. Order Catalogue Piero della Francesca in America February 12, 2013 to May 19, 2013 Revered in his own time as a "monarch" of painting, Piero della Francesca (1411/13–1492) is acknowledged today as a founding figure of the Italian Renaissance. In early 2013, The Frick Collection presented the first monographic exhibition in the United States dedicated to the artist. It brought together seven works by Piero della Francesca, including six panels from the Saint’ Agostino altarpiece — the largest number from this masterwork ever reassembled. They were joined by the Virgin and Child Enthroned with Four Angels, his only intact altarpiece in this country. Piero della Francesca in America was organized by Nathaniel Silver, Guest Curator and former Andrew W. Mellon Curatorial Fellow. Order Catalogue Precision and Splendor: Clocks and Watches at The Frick Collection January 23, 2013 to March 9, 2014 The Frick Collection has one of the most important public collections of European timepieces in the United States, much of it acquired through the 1999 bequest of the New York collector Winthrop Kellogg Edey. This extraordinary gift of thirty-eight watches and clocks dating from the Renaissance to the early nineteenth century covers the art of horology in France, Germany, Switzerland, and the United Kingdom. For reasons of space, only part of the collection can be on permanent view in the museum’s galleries. In 2001, many pieces from the Edey collection were featured in The Art of the Timekeeper: Masterpieces from the Winthrop Edey Bequest, an exhibition organized at the Frick by guest curator William J. H. Andrewes. In 2013, visitors had another opportunity to explore the breadth and significance of the Edey collection through an exhibition that presented fourteen watches and eleven clocks from his bequest. Vincent van Gogh's Portrait of a Peasant (Patience Escalier) October 30, 2012 to January 20, 2013 Vincent van Gogh (1853–1890) painted his Portrait of a Peasant (Patience Escalier) in August 1888 during a highly productive fifteen-month stay in Arles in southern France. The opportunity to display this work in New York is the result of a special exchange program between the Norton Simon Museum, Pasadena, and The Frick Collection and marks the first time in forty years that the painting has left its home institution. Mantegna to Matisse: Master Drawings from the Courtauld Gallery October 2, 2012 to January 27, 2013 In keeping with its tradition of exhibiting masterworks from collections outside of New York, the Frick presented fifty-eight drawings from The Courtauld Gallery, London. This exhibition marked the first time that so many of the principal drawings in The Courtauld's renowned collection — one of Britain's most important — have been made available for loan. The prized sheets represent a survey of the extraordinary draftsmanship of Italian, Dutch, Flemish, German, Spanish, British, and French artists active between the late Middle Ages and the early twentieth century. Gold, Jasper, and Carnelian: Johann Christian Neuber at the Saxon Court May 30, 2012 to August 19, 2012 Since antiquity, gemstones (also known as hard or semiprecious stones) have been cut and polished for use in jewelry, in the creation of vases and cups, and in the decoration of palaces. Rediscovered and developed in sixteenth-century Florence, pietra dura (hard stone) objects were collected and sometimes used as political propaganda among the Medici. A sign of wealth, taste, and power, they were also offered as diplomatic gifts or acquired by foreign sovereigns. Antico: The Golden Age of Renaissance Bronzes May 1, 2012 to July 29, 2012 Antico: The Golden Age of Renaissance Bronzes was the first monographic exhibition in the United States dedicated to Jacopo Alari Bonacolsi, known as Antico (c. 1455–1528). As sculptor to the Gonzaga courts at Mantua and in northern Italy, Antico earned his name, "the antique one," for his creation in the classical style of statuettes, reliefs, and busts that are distinguished by their opulence and beauty. A Passion for Drawings: Charles Ryskamp's Bequest to The Frick Collection February 14, 2012 to April 8, 2012 The Frick Collection celebrated the generosity and discerning taste of former Director Charles A. Ryskamp (1928–2010) with an exhibition of works on paper from his bequest. Dr. Ryskamp's generous gift transformed the museum's holdings in drawings, enlarging them by nearly a third, while complementing the permanent collection's focus on the landscape and figural subjects favored by Henry Clay Frick. The works were exhibited for the first time at the Frick in the Cabinet, a space created by Dr. Ryskamp during his tenure as Director from 1987 to 1997 and intended especially for the display of works on paper. Pages1 Sign Up for E-News! 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2014-15/0000/en_head.json.gz/1239

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Your search for "Frostburg State University Launching Unique Interdisciplinary Major in Ethnobotany" returned 1 possible matches. October 23, 2006 Frostburg State University Launching Unique Interdisciplinary Major in Ethnobotany Only Program of Its Kind in Continental U.S. Integrates Science, Culture Starting in the fall of 2007, Frostburg State University undergraduate students will have the opportunity to major in ethnobotany, a unique interdisciplinary program that examines the connection between people and plants. Currently the only undergraduate program of its kind in the continental United States, the major was approved by the University System of Maryland Board of Regents in June.

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» FSU Foundation’s Annual Fund Awards Financial Support to 26 Proposals From Faculty, Staff and Students News Home FSU Foundation’s Annual Fund Awards Financial Support to 26 Proposals From Faculty, Staff and Students The Frostburg State University Foundation, through its Annual Fund, awarded financial support to 26 project proposals from faculty, staff and students, as part of its ongoing efforts to reinvest in the campus community. Proposals were selected that support the goals of student enrichment, academic enrichment and regional and cultural enrichment, the themes of FSU’s Staking Our Claim: The Campaign for Frostburg. “The FSU Foundation is working very hard to grow the Annual Fund to be more comparable to that of peer institutions so that we can continue putting money back into the campus community and supporting the many great educational experiences our students, faculty and staff are developing,” said B.J. Davisson II, vice president for University Advancement and executive director of the FSU Foundation, Inc. “We intend to increase the Annual Fund so there will be more funding to disperse in this competitive process each year. We believe that this process creates a level playing field in how the campus community can benefit from unrestricted gift revenues.” A total of $75,000 was allocated toward funding proposals, a portion of the $222,269 raised for the unrestricted Annual Fund in fiscal year 2010. Twenty-six out of 52 submitted proposals were selected by the FSU Foundation Board of Directors during a meeting held on June 4. This is the third year the Foundation has made unrestricted gift revenues available to a variety of campus projects proposed by students, faculty and staff. Copies of selected proposals that were awarded funding will be placed on public file in the Lewis J. Ort Library. The project proposals that were awarded funding included: Support for students and faculty to attend conferences and meetings, so they can develop professionally and through scholarship. This year, thanks to the FSU Foundation’s support, students and faculty are attending and presenting at the Association for Advancement of Sustainability in Higher Education conference, the Model Organization of American States, the 24th Annual National Conference on Liberal Arts and the Education of Artists, meetings at the Eastern Psychological Association and the Association for Psychological Science and the regional conference of Phi Alpha Theta, a history honors society with a chapter at FSU. New equipment and supplies for students’ academic enrichment, including a Laminar Flow Hood that will provide a sterile working environment to study tissue culture in animals and plants; equipment that will enable students to collect environmental data from the Cranberry Swamp in Finzel and a variety of human anatomy models that will expand learning opportunities for biology majors interested in health professions. Other selected proposals included funding for equipment to conduct research toward developing novel synthesis techniques for semiconductor nanowires and for the purchase of a laptop cart that will recharge a set of notebook computers and help integrate Web content, digital maps and imagery into the geography class curriculum. A proposal from the Department of Music was also selected for the purchase of new instruments for FSU’s Wind Ensemble and Marching Band. Funds were also awarded to provide support and textbook scholarships to the STEM Program @ Sowers Hall, a freshman experience residence hall for students intending to major in STEM programs. Other selected proposals involving academic enrichment included the program development, professional development and publicity for FSU’s sustainability studies minor, a new minor that will be implemented in fall 2010; a program to pay trained undergraduate students to be in charge of computer labs for FSU’s General Psychology course to provide assistance to other students and facilitate the completion of labs; and a proposal for a Supplemental Instruction project for the Psychology, Math & Closing the Achievement Gap Task Force that will serve students who are struggling in difficult courses. Efforts that focus on enriching the region, including: - FSU’s Children’s Literature Centre, which received support to continue its “Adopt-a-School” program, which gives local children an opportunity to meet and interact with a children’s author/illustrator, to foster literacy development. - FSU’s popular Appalachian Festival and Frostburg’s Mountain City Traditional Arts, which recognize and celebrate the region’s natural landscape, history, culture, food, music and artistic traditions by offering a variety of performances, presentations, workshops and other programming. - FSU’s K-12 Biology Outreach Program, which is working on developing a new program that will invite students and teachers to think about where their food comes from through a variety of experiments and hands-on learning experiences. - The Roundabout Children’s Theatre, which provides FSU students with a variety of professional experiences in designing sets, lighting, costumes, directing and company management through their assistance and involvement and will take two productions on tour to area schools for middle school and elementary school children. - The FSU Center for Creative Writing and its community outreach, volunteerism and interest in bringing writers of national acclaim to the region. - A STEM Day Program organized by the Departments of Physics/Engineering and Biology that requested funds for equipment to facilitate hands-on activities for local students in elementary and middle schools, their parents and their schools. Projects that support student enrichment, including the continuation of FSU’s annual Earth Day celebration; support for E=(LG)², FSU’s student-written and student-edited magazine on sustainability; Frostburg: Take 5, a YouTube contest that invites students to create videos expressing what they love most about FSU; and the development of a journal of sociology that will highlight research and writing of various academic disciplines. The FSU Foundation has embarked on a $15 million comprehensive campaign, Staking Our Claim: The Campaign for Frostburg, to raise badly needed funding for higher education in Western Maryland. Donations to the Foundation support student scholarships and programs, academic programs, faculty development and other critical University needs. For more information about supporting FSU, visit www.frostburg.edu/admin/foundation or call 301-687-4161. Situated in the mountains of Allegany County, Frostburg State University is one of the 13 institutions of the University System of Maryland. FSU is a comprehensive, residential regional university and serves as an educational and cultural center for Western Maryland. For more information, visit www.frostburg.edu or facebook.com/frostburgstateuniversity. FSU is committed to making all of its programs, services and activities accessible to persons with disabilities. To request accommodations through the ADA Compliance Office, call 301-687-4102 or use a Voice Relay Operator at 1-800-735-2258. Office of News and Media Services E-mail: news@frostburg.edu

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October 9, 2008 / Community Bulletin Board RELIGION Outdoor Sing A special outdoor sing will be held again at the home of Dick and Ruth Knepper's on Sunday afternoon, October 12, at 4:00 p.m. Bring a covered dish and a comfortable lawnchair. More... THIS 'N THAT Photo Contest Fulton County Parks and Recreation Commission is accepting photo entries through November 14 with the winning photo to be used in a community art room mural located in the basement meeting room of the Lions Club Community Building. More... MEETINGS PARSE Meeting Pennsylvania Association of Retired State Employees (PARSE) has a 9:00 a.m. breakfast meeting on the second Wednesday of every month at McConnellsburg FOVA (VFW). All retired state employees and spouses are invited to attend. More... FOOD & DINING Ham & Oyster Supper A all-you-can-eat ham and oyster supper will be served October 25 at Cove Valley Youth Camp, Mercersburg. More... HEALTH Diabetes Walk The first annual Multi-County Diabetes Walk will be held October 11, 2008. Registration will be at 11:00 a.m., with the walk starting at noon. The event will be held at McConnellsburg school track. More... RECREATION X Card Shoot X-card shoots will be held Friday nights until November 21, at 7:00 p.m., at Fulton County Rifle and Pistol Club. Enter to win a New England Arms 12 gauge pump shotgun when playing X card. More... FALL FOLK FESTIVAL ACTIVITIES Fall Folk Festival Vendors There is both indoor and outdoor vendor space available at the Fall Folk Festival Welcome Center at the Lions Club building, 301 East Maple Street, McConnellsburg. More... REUNIONS FR Class Of 1963 Reunion Forbes Road Class of 1963 will hold its 45-year reunion on November 8, at 5:00 p.m., at New Fort Family Restaurant in Fort Littleton. More information may be obtained by calling 717-485-4713 evenings after 6:00. More... BINGO Red Neck Basket Bingo Red Neck Basket Bingo to save the old high school building will be held Saturday night, November 22. Doors open at 5:30 p.m. and bingo starts at 6:30 p.m. in the old MHS High School Gym. A total of 24 games for $ 25.00. More...

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-A A +A By The Staff Thursday, April 30, 2009 at 12:00 am As I began to write this week's column, I tried to recall in years, March and April with weather like we have had this year. With another front moving through this past week, high winds and more rain stopped fishing for the most part. The lake level is normal; however, the water is still heavily stained but seems to be clearing.

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Local colleges Lakeview alum Pruett rolling after slow start For The Times GREENWOOD, S.C. — David Pruett came to Lander with a reputation of being a stellar 3-point shooter. But of his first 32 shots from behind the arc this season, he made only six.And what was the response from his coaches and teammates?Keep shooting.Pruett, a Lakeview Academy graduate, has dramatically shaken off the slow start as well as a foot injury and has won two of the last Peach Belt Conference Player of the Week awards.“First, I’d like to thank my teammates because without them I wouldn’t have been able to accomplish Player of the Week even once, let alone twice,” the 6-foot-4 sophomore wing said. “I feel very honored and hope to win it a few more times here at Lander.”Pruett’s Player of the Week honors were no-doubters. Last week, the Armstrong Atlantic State transfer averaged 27 points per game in leading the Bearcats to victories over Hiwassee College and Lenoir-Rhyne in Lander’s Bearcat Holiday Classic.He started the week with 26 points against Hiwassee, then came back and put up 28 against Lenoir-Rhyne. Pruett shot 58 percent (15 of 26) from the field and 55 percent (11 of 20) from 3-point range. He also shot 87 percent (13 of 15) from the foul line while averaging 4.5 rebounds and 2.5 steals in those two games.“We are very excited for David to be named Peach Belt Conference Player of the Week for the second time,” Bearcats coach Jeff Burkhamer said Wednesday morning. “He is very deserving and has earned the honor by playing well.“David’s outstanding play has really helped our team score and has led to some terrific wins. Our team believes in David and has tremendous confidence in him shooting the ball. We are shocked when he misses an open shot.”Three weeks earlier, Pruett scored a career-high 34 points in a 98-91 victory over Southern Wesleyan to earn Player of the Week for the first time. He hit 11-of-19 shots from the field and seven of 12 from behind the arc to go along with all five of his free throw attempts. He also grabbed six rebounds and blocked one shot.His 34 points are the most scored in a single game in the Peach Belt so far this season and the most from a Lander Bearcat since Adrian Penland, a West Hall graduate, scored 38 against Allen University during the 2002-03 season.Pruett has climbed to sixth on the PBC scoring chart with 16.6 points per game and is fourth in the league in 3-pointers made per game.His ascent up the league scoring ladder is no surprise given Pruett’s solid scoring reputation.Pruett averaged 21.7 points per game as a senior at Lakeview and is the school’s second all-time leading scorer with 1,961 points.Burkhamer, then at Armstrong Atlantic, recruited and signed Pruett to play for the Pirates. After two years, Pruett reunited with his former coach for Burkhamer’s second season at Lander.“Coach Burkhamer recruited me to Armstrong in 2008. My freshman year, Coach and I agreed the best thing for me to do was to redshirt,” Pruett said.Pruett played last season for the Pirates and had a solid year, leading AASU in 3-point field goal percentage while finishing fourth in the Peach Belt. He played 20 minutes per game, shooting 42 percent from behind the arc. He averaged eight points and three rebounds per game and had a career-high 21 points versus Clayton State.Pruett, the leading returning 3-point shooter in the PBC this season, left after two years in Savannah and has already surpassed his career high three times while at Lander.“When coach left Armstrong after that (2008-09) season, I missed his system,” Pruett said. “So, after my first season playing at Armstrong, I asked for a release and visited Lander.”The decision was not easy.“Armstrong was a fantastic experience for me,” he said. “I wouldn’t take anything back from the two years I spent there. I had ample amounts of playing time, so that was not an issue.“After visiting Lander, I knew it was the place for me. The student body and the faculty, as well as the City of Greenwood are all very supportive. They really turn out for the games here. The facilities are top notch. Plus, Coach Burkhamer is here.”“David is a leader and he already knows what to expect from me and knows how we do things,” Burkhamer said of Pruett’s transfer. “We are counting on him to be a leader because of the number of new faces we have.”The transition has not been easy, however. First, Pruett and teammate Dawda Njie, also transferring from Armstrong, were joining a team that was not only new to them, but pretty much new to everybody.Lander had only one returning player, Tovi Bailey, from last season. Therefore, Njie, who had very limited playing time with the Pirates, and Pruett were the only players who had ever played together before.“Early in the season, we were learning how to play with each other,” said Pruett, who is majoring in Mass Communications. “We’re continuing to learn about each other and we’re working very hard to improve as a team.”Pruett’s transition was slowed by a left foot sprain in the fall, and it “was tough to get back into the flow,” he admitted.In fact, Pruett missed Lander’s first two games of the season versus Newberry and Voorhees. His first game with the Bearcats was against Erskine and he did well, scoring 18 points including four 3-pointers.But then came a three-game stretch against UNC Pembroke, Winthrop and Montevallo where he struggled shooting the ball, going 6-for-29 overall and 2-for-23 from behind the arc.He was one of nine from long range against Pembroke, missed all four attempts at Winthrop, and hit only one of eight against Montevallo.After going 4-for-11 against Erskine, the next three games left him six for 32 from behind the 3-point line on the season, or 19 percent.“Well, it was tough coming back from the injury. I was in a shooting slump,” Pruett said.“The coaching staff and my teammates would not let me get down on myself. They believe in me as I believe in them.”“David did not shoot the ball well early in the year and I think a lot of it had to do with his foot injury,” Burkhamer said. “He was favoring one foot more than the other and it was affecting his shot. We noticed that he was turning his body and coming down with his feet turned to a side instead of keeping his feet straight and aimed at the rim. Once his foot healed, he starting shooting with his feet straight and his shot came back.”Pruett added, “As I got to feeling better, coach Burkhamer helped me tune up my shot where it was prior to the injury. Eventually, I just went on the court and started hitting some shots.”The turnaround was remarkable. He hit two early 3s at Georgia College & State University, and that was a sign of things to come. Pruett nailed 7-of-12 long-range shots against Southern Wesleyan, 5-of-9 versus Hiwassee, and 6-of-10 against Lenoir-Rhyne.Pruett is now 26-for-68 (38 percent) from 3-point range after the very slow start, and has made 18 of his last 31 (58 percent).Pruett has also done his fair share inside the arc, making several plays defensively during Lander’s last three games, all victories. “But I still have much to improve on defensively,” he said.More importantly, he scored Lander’s final eight points to help the Bearcats hold off Lenoir-Rhyne last Thursday, including five of six free throws in the final minute plus. He is now 27-for-31 from the line (87 percent).“I never worried about David’s shooting percentage early in the year because I’ve seen him shoot the ball and know he can make shots,” Burkhamer said.“Shooters sometimes go through stretches where they miss shots, but eventually they come out of their slump. I knew he would too. He just needed to get well and then have a breakout game. He did that and now he is rolling.”Burkhamer is clearly excited to have Pruett back on his side.“I think David is one of the best shooters in the Peach Belt Conference,” he said. “He is terrific on catch and shoots, he can pull up and hit a shot, he shoots the deep 3, and he is an outstanding free throw shooter. He has beautiful mechanics on his shot. We are excited that David is a Bearcat and glad we have him for a couple of more years.”

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Medicare: The problem is producing more grads, not increasing fees for doctors By Wayne Madsen December 18, 2011 12:30 a.m. Read the other side: Reasonable reforms can give fair fees and ensure patients receive quality treatment by Rep. Tom Price. The latest scare tactic by right-wing opponents of the Affordable Care Act aims at convincing Americans that reasonable trims in Medicare spending will make it very difficult for seniors to find a good doctor in coming years. A lot of this hooey is based on an outdated 2008 report from the Medicare Payments Advisory Commission that 29 percent of the Medicare beneficiaries who were looking for a primary care doctor had a problem finding one to treat them, up from 24 percent the year before. Please note that the report by the independent federal panel that advises Congress on Medicare was issued the year before the House and Senate passed the Affordable Health Care and made it the crowning achievement of President Barack Obama's first-term. There's no doubt that some doctors are leaving Medicare, but many do so in order to band together to form small concierge clinics that cater to wealthy seniors. These posh clinics are designed to cater to the top 1 percent of the nation's elderly - the ones who can pay boutique prices and prefer not to sit next to the riff-raff in germ-filled waiting rooms. There's no doubt some physicians are leaving the Medicare system, but they hardly constitute the mass exodus that free-market advocates imply. A survey reported in the June 27 Archives of Internal Medicine found that physician acceptance of new Medicare patients fell to 92.9 percent in 2008 from 95.5 percent in 2005, while more recent survey in early October by the Texas Medical Association reported 3 percent of its members withdrew from the federal program. If there are serious doctor shortages looming in our future, they are more likely attributable to the rapid growth of people over 65 rather than a flight of health-care providers. Some 40 million Americans currently have Medicare insurance, but they will be joined soon by an additional 70 million Baby Boomers. The United States needs to increase significantly the ranks of its medical school graduates or begin to import more from abroad. As for the doctors who would rather ignore their Hippocratic oaths to serve the poor as well as the rich, they will evoke few cries of pity from most Americans. While the proposed cuts in Medicare payments would cut a few percentage points from their income, they are hardly bound for the poor house. American physicians across all categories make far more than their counterparts in any other country including such affluent ones as Germany, Japan, Britain, France, Denmark and Sweden. Consider the median salaries as recently catalogued by the American Medical Group Association, which has been tracking the salaries of U.S. physicians since 1986. They range from $204,000 for practitioners of family medicine to $605,953 for orthopedic surgeons who specialize in joint replacements. In between are anesthesiologists at $370,500, dermatologists at $375,176, gastroenterologists at $405,000, and radiation therapists at $447,250. Bear in the mind that those are median salaries with half of all doctors making more and half making less. By comparison, the median household income in the United States is $46,623. The fact that a relative handful of doctors are quibbling about slight cutbacks to their incomes at a time when 20 million Americans are unemployed or underemployed can be laid at the doorsteps of President Obama, Senate Majority Leader Harry Reid and former House Speaker Nancy Pelosi. Instead a of pushing for a low-cost, single-payer health-care system when Democrats controlled Congress in 2009, the trio couldn't forgo millions of dollars in campaign contributions from Big Pharma, Big Insurance and powerful physician groups. If they had, Americans might now be enjoying the low-cost, highly effective national health insurance that has been available for decades to the citizens of Canada, Japan, the European Union and virtually every other advanced nation on Earth. Indeed, if that system were in place now, no greedy doctor would be able to turn his back on the needy. The biblical admonition "physician heal thyself" seems apropos. Wayne Madsen is a contributing writer to www.onlinejournal.com.

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Interviews » Riding The Current of Brendan Rivera’s Ocean Interviews Brendan RiveraInterview Related Posts Unraveling Detar A Parking Lot Phone Call with Eron Bucciarelli of Hawthorne Heights Staying True to Punk Roots The Real Issues Riding The Current of Brendan Rivera’s Ocean Jun 27, 2012 in Interviews | 0 comments In a scene where it is becoming immensely harder to distinguish one band from another, Brendan Rivera pitches a signature curve ball which defies all expectations of current alternative music. Although reviewers describe Rivera in the neighborhood of Mumford & Sons, Good Old War and Jimmy Eat World, Rivera doesn’t quite conform to the typical mainstream acts who are rapidly gaining popularity. Through the seven minute long track “No Ocean in Ireland,” titled after his latest release, Rivera ignores the fear of possibly overwhelming listeners. Instead, he presents his audience with a shade of irony which immediately sets the tone of the entire album. “It’s like a blatant lie that somebody can tell somebody,”commented Rivera about the album’s title.“That’s just kind of like the irony of somebody telling you something that is completely false.” Throughout the song, Rivera reveals a story of two people who are in a relationship and separated by an ocean. The story takes a step back through history as Rivera describes a timeperiod when there weren’t phones and a severe lack of communication. As the opener comes to an end, Rivera stated how the story is, “This one guy’s journey to go across the ocean and meet up with this person and they are going to meet up in their dream home, their kingdom.” By the album possessing a strong sing-a-long nature, No Ocean in Ireland delivers a more compact collection of songs composed by Rivera. According to Rivera, the latest album offers “more of a distinct story line,”compared to his earlier work. “The last album was like a mix tape and just put together,” continued Rivera. “I wanted everything tied together a little more. I had more of a direction going into the writing process.” Rivera gained popularity through his previous band Looking Glass Wars, a band whose material was actually his first solo album under a different name. “With this album, I had a 12 string guitar and just wrote the entire thing just sitting in my living room or in my room. I like it better that way because I can sit there and think by myself.” Compared to writing with the members of Looking Glass Wars, Rivera revealed his “stubborn” attitude towards writing music is associated with his own self-evaluation.“I have a specific style that I am going for, something in my head and if it doesn’t sound that way, I’m not very happy with it,” said Rivera. The desire to express inner feelings is one of Rivera’s strongest motivations towards writing music.“Anger and frustration mostly comes with not being able to express yourself the way you want to,” said Rivera. “Just playing something, just doing something, and just letting it out. That always gets me to pick up a guitar and try to wail.” Bearing resemblance to the darker tone of Matt Skiba from Alkaline Trio and Anthony Raneri from Bayside, Rivera’s voice offers a melancholy character while still possessing a celebratory spirit. “I guess anything that kind of sounds a little sugarcoated, sarcastic and a little dark I think would have comparison to me, which I kind of like’ said Rivera. “I like things that sound kind of happy but meaningfully they are kind of dark and have that split feeling.” Signed to Veggie Co. Records, Rivera described the label as a partnership and as a really good friendship. Unlike Rivera’s previous releases, the new album was instead produced by Greg Dunn of the band Moving Mountains. “I was kind of going for more of a wall of sound, like a dreamy atmosphere which I felt like I could have gotten from Greg Dunn. I liked their sound and I felt like we could definitely use a little bit of his touch on the album.” Inspired by the drumming of Scottish band We Were Promised Jet Packs, Rivera wanted something of equal relevance. “One thing I liked about them is there toms and bass drums were so loud and powerful,” said Rivera. “I said, ‘let’s get really powerful toms and really powerful bass drums, let’s get something we could feel.’” When finding bands to share the stage with, the issue of similarity is something stored in Rivera’s mind.“You had Brand New and Taking Back Sunday who were coming up together. Even if you want to get into pop punk or stuff like that you had The Movielife and Midtown or even Alkaline Trio, I’m sure they had somebody else like H20. All these bands had their little scene. That’s something that music needs. It has at points, it has these bands that tour with each other all the time and they’re buddies. That’s how music should be. You should help each other out as you get bigger.” In the essence of helping buddies out, the gang vocals at the end of “Sands of Ours” may be the most inspiring element of the album. “I felt like a lot of my friends, and with myself, we were going through a lot of the same things at the same time,” said Rivera.“I was trying to make something that we all kind of were going through and understood and we could sing it together. That line is something that you could just scream at somebody…we all scream together.” While not performing on stage, Rivera’s self-expression continues to linger through his role as a guitar instructor. “I used to not be able to play, I used to not be able to sing, I used to not be able to write the way I feel like I can express myself,” said Rivera in regards to what he tells his students. “So now that I can do it, all I want to do is take advantage of it and get better at it and maybe one day be playing with people that I’ve looked up to all my life.” By Nick DeLibero Album Review: Skrillex ‘Recess’ The Devil Wears Prada Headline The 2014 Sub City Take Action Tour Events: Modest Mouse with Brand New to play Brewery Ommegang Poor Kelly, Poor Me Love and Receive Love Escapist Records and Pure Noise Records To Co-Release New Two-Song 7” From Daybreaker Moving Mountains Announce New Album Sleepy Turtles – Summer, Hither (EP) Stay Updated Enter your email to receive updates from Gaining Ground Media as they go live.

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Your browser does not support iframes. Read a digital copy of the latest Galax Gazette online. Health problem caused fatal crash -A A +A By Christopher Brooke, Reporter Thursday, May 14, 2009 at 12:00 am (Updated: June 21, 8:50 am) HILLSVILLE — A former commercial truck driver's seizure behind the wheel apparently resulted in a fatal head-on collision between two tractor-trailers on Interstate 77 in Carroll County on Feb. 17.

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» Forums » TECH SUPPORT » GLITCHES, BUGS & PATCHES » 45 Free and Useful Windows Applications 45 Free and Useful Windows Applications Re: 45 Free and Useful Windows Applications [Re: Donald] Thank you for the link Donald. _________________________ BobH Loc: 47.79N, 122.24W Good stuff Donald. I was aware of many of these and use some of them but it's nice to see them all in one place.My personal recommendations for applications that I use all the time are FileZilla and Notepad++. BobI've learned that if you're too busy to help a friend, you're too busy. Thanks Donald _________________________ bigmamma1 Don-This site is a treasure trove of useful things (free downloads,advice,news,ect) for anyone who wants to get the most out of a computer-even a non geek like me can use it! People do not remember how much you know,only how you make them feel finished Gray Matter, playing Alice Madness returns and Deponia

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Available for: PlayStation 3, Xbox 360, PC, Wii U Assassin's Creed III Images All Assassin's Creed III Images Assassin's Creed III Videos Assassins Creed III - Gameplay For PC, PS3, Xbox360 We go after a chest, and some soldiers pick on the wrong guy! Assassin's Creed III - Killing Spree More footage from our gaming of Assassin's Creed III Assassin's Creed III - Flawless Victory For PC, PS3, Xbox360, WIIU Our own little gameplay footage from the game... We take on the world and win!!! The year is 1775. The American colonies are about to revolt. You are Connor, an assassin who has sworn to secure liberty for his people and his nation. To do so, you will hunt your enemies across a staggeringly large, open, and realistic world. You will unleash your lethal skills in a violent quest that will take you from chaotic city streets to blood-soaked battlefields in the hostile American wilderness and beyond. You will meet legendary heroes of American history, and together you will conspire to annihilate those who threaten Liberty itself.Whether you use your predatory instincts to kill silently, or your fearsome arsenal to kill openly, one thing is clear: the world that the Assassins live in has become far more deadly. And so have you. http://assassinscreed.ubi.com/ac3/

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Screenshots and Images for Star Wars: Knights of the Old Republic The latest screenshots, artwork, photos, and other images of Star Wars: Knights of the Old Republic for . 3 4 5 Read more and connect with us About Star Wars: Knights of the Old Republic Related to Star Wars: Knights of the Old Republic Screenshotsfor Star Wars: Knights of the Old Republic

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Steam Holiday Sale Continues, Call of Duty: Black Ops 50% Off I'm going to be pretty honest, today's Steam holiday sales aren't exactly anything to write home about. Last year's Call of Duty is half price (Call of Duty: Black Ops - $29.99), which is a fair deal, but you can expect the price to continue dropping now that Modern Warfare 3 has landed. The entire F.E.A.R. Collection can be had for $24.99 (50% Off) , which again is a fair price for the batch of well-recieved shooters, but not blowing our mind's here. Probably the best deals today are on the Prince of Persia series, with each game discounted 75%. If you've never played Sands of Time, $2.49 is a heck of a bargain, and you can skip over the schlock which is Warrior Within and move straight on to the third installment of the original trilogy: The Two Thrones, also clocking in at just $2.49. More notably, you've still got three hours to snag yesterday's deals, including Sonic Generations for $10.19, Bastion for $5.09 and indie gem Terraria for just $2.49. Those are some prettty savage discounts on some very awesome games, so do check them out. Also, anybody got coal to trade? One more and I get a gift! - Vito Gesualdi (endlesschris on Steam)

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BioWare producer: More surprises in store for SWTOR fans 'next year' Earlier today, BioWare and EA announced the first digital expansion for Star Wars: The Old Republic. Titled Rise of the Hutt Cartel, the new add-on raises the level cap to 55 while adding a brand new storyline involving the merciless Hutt Cartel. In the expansion, players travel to the dual-faction planet of Makeb which is shaping up to be one of the "most breathtakingly beautiful settings" in Star Wars: The Old Republic. BioWare didn't reveal too many details, but did promise an "epic and exciting" clash with the Hutt Cartel. Apparently, that's just the "tip of the iceberg" for BioWare and Star Wars: The Old Republic, which recently began offering a free-to-play option after subscription numbers began dwindling. "We have a lot more surprises in store for our fans next year!" teased BioWare Austin Executive Producer, Jeff Hickman. Hickman stopped short of revealing any details, but for Rise of the Hutt Cartel is definitely a good start. What sort of surprises or announcements would you like to see in the future for Star Wars: The Old Republic? Tags: Star Wars: The Old Republic SWTOR Game Update 2.7 'Invasion' now available Star Wars: The Old Republic 'Invasion' Game Update 2.7 coming next Tuesday Star Wars: The Old Republic expansion 'Galactic Strongholds' announced SWTOR 'Galactic Starfighter' available to all; two more expansions coming in 2014 Star Wars: The Old Republic update 2.4 'The Dread War' releasing Oct. 1 Yub Nub: Ewok companion coming to Star Wars: The Old Republic Star Wars: The Old Republic subscriptions gone, revenue up Star Wars: The Old Republic 'Rise of the Hutt Cartel' launches next month About Star Wars: The Old Republic Mass-Multiplayer Online (MMO), Role-Playing Game (RPG) Related to Star Wars: The Old Republic Newsfor Star Wars: The Old Republic Screenshotsfor Star Wars: The Old Republic Star Wars: The Old Republic's Game Update 2.7, titled... Star Wars: The Old Republic Game Update 2.7, dubbed "Invasion,"... BioWare's Star Wars: The Old Republic is getting a new...

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Shin Megami Tensei: Persona 3 Portable preview Posted by: Steven Hopper When it released back in 2007, Persona 3 was a critical darling, quickly becoming one of the highest-rated games for the system, and thrusting the series into the upper echelon of RPGs. A year later, Atlus released an updated version of the game, Persona 3: FES, which also met with great acclaim, and offered some great additions over its predecessor, including a new chapter. Now, Atlus is preparing to release the third version of the game, albeit in handheld form with Persona 3 Portable.Coming for the PSP through retail and digital distribution, Persona 3 Portable condenses the original smash hit to fit on the system. There are some cuts to be found here and there; the extra chapter (The Answer) from Persona 3: FES is not on offer here, and the game’s anime cut scenes have been replaced with in-engine scenes and still images. However, most of what made the original game (and its subsequent upgrade) so great is on offer here, including the solid dungeon-crawler-meets-high-school-chat-sim hybrid gameplay and even some features that aren’t found in the PS2 versions. If you are a fan of the Persona games or you missed out on the original Persona 3 (twice), then this could be one that you’ll want to look out for.For the uninitiated, Persona 3 follows a group of Japanese students as struggle to defeat evil forces every night during a phenomenon known as the Dark Hour, where people are transformed into coffins and have no recollection of the events that take place at that time. However, your group of teens isn’t affected by the Dark Hour, and instead utilizes creatures, known as Personas, to fight off evil beasts while discovering the machinations behind the events that are taking place.Much of the game takes place through dialogue chains between your main character and others that he (or she) meets. Depending on the choices you make while speaking to other characters, you can earn special boosts called Social Links. These Social Links as they are called will also net you some performance boosts with your Persona as well, granting them higher stats.The other side of the gameplay coin has you exploring the floors of the tower of Tartarus and taking on enemies. This plays out fairly traditionally, employing a turn-based mechanic for your character, while your cohorts’ actions are picked up by AI tactics that you can equip for them. Your Persona will give you specific abilities to use in battle, which can be upgraded as you progress and gain experience.The biggest addition that Persona 3 Portable brings to the table is a playable female character. At the beginning of the game, you’ll choose to play as a male or a female character, offering up a different view of the game’s plot. The game’s storyline and gameplay elements are pretty much the same whether you go male or female, but this is nevertheless something that the PSP version has over its PS2 counterparts.There are some corners cut in the handheld version, but for the most part, this PSP iteration nails what made the original PS2 game so great. Look for a full review of the game closer to its release. Ghostlight to bring console JRPGs to PC Atlus discounts ten games in a "Re-Vita-lized" sale on PSN Persona 2 Remake Delayed in Japan New Catherine Gameplay Trailer Details More Sexual Tension and Block-Pushing Catherine Special Edition to Include Pillow, of Course Persona 3 Portable is Now Available in Stores and on PlayStation Network Atlus Reveals Pre-order Bonus "Junpei" Baseball Cap for SMT: Persona 3 Portable Persona 5: What We Want To See About Shin Megami Tensei: Persona 3 Portable Related to Shin Megami Tensei: Persona 3 Portable Newsfor Shin Megami Tensei: Persona 3 Portable Screenshotsfor Shin Megami Tensei: Persona 3 Portable Ghostlight, the European publisher of a number of Shin Megami Tensei... Download these games at lower prices for your PSP or Vita When Shin Megami Tensei: Persona 3 released in North America, it hit gamers...

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Welcome to jeff1's Member Page I live in: United States First registered on May 15, 2007

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Experience Daniel Kim's Epic Mashup of the 68 Best Songs of 2013 By Stacy Lambe Dec. 4, 2013, 12:50 a.m. It's that time of year again when the Internet's favorite DJs crank out their year-end mashups. Both DJ Earworm and Daniel Kim released their epic mixes, but it's Kim's mix that's making the grade. This year he outdid himself by mashing together 68 songs from the past year in less than six minutes. It's a surprisingly terrific mix that makes Miley Cyrus' tired shtick less annoying, and keeps those exhausted by Robin Thicke's "Blurred Lines" from jumping out of the window. Watch/listen/experience below. In case you couldn't identify all the songs, check out a full list below: Anna Kendrick – “Cups (When I’m Gone)” Armin van Buuren feat. Trevor Guthrie – “This Is What It Feels Like” A$AP Rocky feat. Skrillex, Birdy Nam Nam – “Wild For The Night” Avicii – “Wake Me Up” Avril Lavigne – “Here’s To Never Growing Up” Bastille – “Pompeii” Bauuer – “Harlem Shake” Bingo Players feat. Far East Movement – “Get Up (Rattle)” Britney Spears – “Ooh La La” Britney Spears – “Work B**tch” Bruno Mars – “Locked Out Of Heaven” Bruno Mars – “Treasure” Bruno Mars – “When I Was Your Man” Calvin Harris feat. Ayah Marar – “Thinking About You” Calvin Harris feat. Ellie Goulding – “I Need Your Love” Capital Cities – “Safe And Sound” Daft Punk feat. Pharrell Williams – “Get Lucky” Demi Lovato – “Heart Attack” Drake feat. Majid Jordan – “Hold On, We’re Going Home” Drake – “Started From The Bottom” Ellie Goulding – “Burn” Icona Pop feat. Charli XCX – “I Love It (I Don’t Care)” Imagine Dragons – Demons Jason Derulo – “The Other Side” Jay-Z feat. Justin Timberlake – “Holy Grail” Justin Timberlake – “Mirrors” Justin Timberlake feat. Jay-Z – “Suit & Tie” Katy Perry – “Roar” Kelly Clarkson – “Catch My Breath” Ke$ha – “C’mon” Ke$ha feat. will.i.am – “Crazy Kids” Krewella – “Alive” Lady Gaga – “Applause” Lana Del Rey – “Summertime Sadness (Cedric Gervais Remix)” Lorde – “Royals” Macklemore & Ryan Lewis feat. Mary Lambert – “Same Love” Macklemore & Ryan Lewis feat. Ray Dalton – “Can’t Hold Us” Maroon 5 – “Daylight” Maroon 5 – “Love Somebody” Martin Garrix – “Animals” Martin Solveig & The Cataracs feat. Kyle – “Hey Now” Miley Cyrus – “We Can’t Stop” Miley Cyrus – “Wrecking Ball” Naughty Boy feat. Sam Smith – “La La La” One Direction – “Best Song Ever” One Direction – “Story Of My Life” OneRepublic – “Counting Stars” OneRepublic – “If I Lose Myself” Passenger – “Let Her Go” P!nk feat. Nate Ruess – “Just Give Me A Reason” Pitbull feat. Christina Aguilera – “Feel This Moment” Pitbull feat. Ke$ha – “Timber” Pitbull feat. TJR – “Don’t Stop The Party” PSY – “Gentleman” Rihanna – “Pour It Up” Rihanna feat. David Guetta – “Right Now” Rihanna feat. Mikky Ekko – “Stay” Robin Thicke feat. Kendrick Lamar – “Give It 2 U” Robin Thicke feat. T.I., Pharrell Williams – “Blurred Lines” Selena Gomez – “Come & Get It” Selena Gomez – “Slow Down” Taylor Swift – “22” Taylor Swift – “I Knew You Were Trouble” will.i.am feat. Britney Spears – “Scream & Shout” will.i.am feat. Justin Bieber – “#thatPOWER” Ylvis – “The Fox (What Does The Fox Say?)” Zedd feat. Foxes – “Clarity” Zedd feat. Hayley Williams – “Stay The Night”

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Friday April 2, 2010 12:14 pm Microsoft smartly removes ‘Series’ from Windows Phone 7 No, this isn’t the most exciting story about mobile devices this weekend, but we’ve gotta hand it to Microsoft for listening to the masses on the whole Windows Phone 7 Series branding. It was too long, there was no simplicity, and frankly, it made no sense. Rather than stubbornly sticking with it, they’ve heard our cries, and Windows Phone 7 Series is now simply known as Windows Phone 7 from here on out. This doesn’t change the hardware or software in any way, mind you, it’s strictly a branding change. A smart branding change. microsoft, rebranding, smartphones, windows mobile, windows phone 7, windows phone 7 series

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Christmas Gift Ideas: Black Diamond New Arrivals Jewelry From $250 to $499 About Christmas Gift Ideas: Black Diamond New Arrivals Jewelry From $250 to $499

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Inspiring a New Generation of Engineers FIRST LEGO League and Junior FIRST LEGO League (left to right, from front row): Isaac Che, Elizabeth Che, Joseph Chaney, Zachary Labon, Rebekah Cox, Kira Labon, Peter Collings, Noah Hitchcock, Caleb Lutz, Jacob Lutz, Jonah Hitchcock, Fiona Chaney, Joel Dille, Ben Che, James Lutz, Elly Frey, Caleb Collings, Jared Lewis In the hallways of Geneva College’s Science & Engineering (S&E) building, college students are preparing for careers in science, technology, engineering and math (STEM). But they aren’t the only ones. In the fall of 2009, a group of elementary- and middle-school students designed, built and programmed a robot to compete in FIRST LEGO League, a worldwide competition designed to build character and inspire kids to pursue the STEM fields. The inspiration behind this team began with a discussion among a group of homeschooling moms in the Beaver Valley. Julia Chaney ’92, home educator, Geneva psychology grad and daughter of now-retired Spanish professor Dr. Richard Evans, thought the FIRST competition would be a great opportunity for the kids’ educational and personal growth. “It’s not just about robots, but also about how children of all skills, levels and abilities work on a problem together,” Chaney says. “I love that. FIRST Robotics helps kids believe they can go into the STEM careers.” The team (ages 9 – 13) called themselves the Golden Arrows and registered for Pittsburgh competition, which would be held at Carnegie Mellon University National Robotics Engineering Center in December. The topic for this year’s competition was “smart moves.” “The children were challenged to design a robot to accomplish various tasks on a large table-top game board/field set-up. The robots could be designed to complete any mission on this field set-up in order to accumulate points,” Chaney says. One of the team members was Isaac Che, the son of Geneva College engineering faculty David Che. As soon as Che heard about the project, he thought it would be great to get Geneva students involved as mentors. Senior mechanical engineering major Joel Dille was the first to respond to Che’s request for a student mentor. With his love for kids and robotics work, the opportunity seemed like a perfect fit. However, Joel didn’t realize that the students would be so young. He was a little overwhelmed at first, but it didn’t take him long to settle in and enjoy the experience. “Joel, together with my older son Benjamin, would come on Friday evenings after class to work with them on their robots’ programming,” Che says. The Golden Arrows’ research project topic was to transport mobile surgical units, especially to mountainous places where it’s difficult for planes to land. The mentors’ primary job was to help the kids with design and programming. There was a pretty steep learning curve in those areas, but the youngsters’ creativity made up for much of the knowledge they lacked. “All of the kids had excellent design ideas. I love the imagination of children,” Joel says. Joel and Ben worked with the kids throughout the fall semester, and Julia’s brother Rich Evans ’90, a Geneva engineering graduate who now works for NASA, also came several times to volunteer and coach the team. All the long hours of hard work paid off, and by the time the December competition rolled around, the robot was ready to go. There were 72 teams at the competition, and each had to compete on the same field set-up. The competition also included an oral presentation. The Golden Arrows came in 52nd out of 72 on the challenge course, but they placed 20th overall. That was a good result for a first-year team. Students in the FIRST LEGO League participated in the December competition (left to right from front row): Isaac Che, Peter Collings, Jacob Lutz, Fiona Chaney, Joel Dille, Ben Che, Noah Hitchcock, James Lutz, Elly Frey, Caleb Collings, Jared Lewis “This was not just a robotics competition—it was a combination of all the skills needed to go into these STEM fields,” Chaney says. “Students are judged 25 percent on their robot’s performance, 25 percent on design, 25 percent on research and 25 percent on teamwork.” The FIRST LEGO League competition is held every fall, and by September 2010, the team plans to be back in the competition designing a new robot. And maybe—in a few more years—some of those kids might be students at Geneva College, getting ready to put research, teamwork, knowledge and imagination to the test in STEM careers. http://www.geneva.edu/object/nr_new_generation_engineers_5_10.html

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HomeErwin Jekelius, Doctor (1905 - 1952) Geni requires JavaScript! Please enable JavaScript in your browser's settings to use this part of Geni. Erwin Jekelius, Doctor (1905 - 1952) ‹ Back to Jekelius surname Is your surname Jekelius? Research the Jekelius family Erwin Jekelius, Doctor's Geni Profile Records for Erwin Jekelius Hermannstadt , Austria in Russia Blasenkrebs Managed by: mi² Anderson Paula Hitler / Wolff ex-partner About Erwin Jekelius, Doctor http://gedenkstaettesteinhof.at/en/exibition/10-diagnosis-useless Former partner and engaged to Paula Hitler / Wolf, but never married. Dr. Jekelius was head of the Am Steinhof Psychiatric Institution in Vienna [Psychiayrisches Krankenraus Der Stadt Wiem] where Aloisia Veit, Hitler's second cousin, was confined for nine years. Paula's fiance was a willing executioner in the program of mass murder they called "euthanasia." He sent over 4,000 patients to the gas chambers. Hitler's sister knew about it. Yet she still wanted to marry the doctor. She asked her brother's permission. But only Hitler would decide who was part of the family. He had Paula's fiance arrested, and sent to the Eastern front. Erwin Jekelius was taken prisoner by the Soviets. He died in captivity in 1952. Berchtesgaden, 1958. Hidden camera footage of Paula Hitler, alias Paula Wolf. She lived on social security on her own. Only a few locals knew who she really was. That same year, director Peter Morley made a documentary about the Nazi dictatorship. He interviewed people who had been close to Hitler. Tyranny, the Years of Adolf Hitler. It was the first and last television interview with Paula Hitler. Translated Text Erwin Jekelius (born June 5, 1905 in Sibiu, † 8 May 1952 in the Soviet Union) was an Austrian psychiatrist and neurologist at the time of National Socialism and as T4 euthanasia expert in crime involved. Jekelius, a medical doctor in 1931 received his first appointment at the Special Education Station of the University Children's Hospital in Vienna, where he worked until 1936. From 1933 Jekelius member of the NSDAP and the Patriotic Front. At the instigation of the President of the Evangelical Church Council obtained upper Jekelius employment as a medical officer of the City of Vienna. From 1938 he was initiated specialist in nervous diseases and in Vienna from beginning of November 1938 the acting clinic for neurological disorders of the workers health insurance fund. He also took over from 1938, initially acting and from 20 March 1939 official line of drinkers sanatorium "Am Steinhof" in Vienna. After the outbreak of World War Jekelius was drafted into the armed forces, but in mid April 1940 in the Main Health Office of the City of Vienna busy, where he dated 2 June 1940 to early August 1941, the Unit for the mentally ill, addicted psychopaths and care "initiated. Has commenced a preliminary investigation at this time because of fornication against nature to Penal Code § 129 was discontinued in August 1940. [3] Of 24 July 1940 to 1941 was Jekelius worked at the Vienna city youth reformatory "At the basic level" as the medical director. During the Second World War were in the children's department of the institution in the context of child euthanasia at least 789 disabled and / or behavioral problems children killed by administration of hypnotics, due to malnutrition or hypothermia [4]. Of 14 October 1940 to Jekelius worked in the T4-T4 as a witness report forms of patients and decided from files which patients in the Nazi killing centers as "euthanasia case" should be gassed. Jekelius also worked with other doctors in a euthanasia law ("law on euthanasia for terminally ill patients") with. [2] This law was adopted in October 1940, but gained no legal validity. Jekelius the year 1941/1942 was released from his position as director in the institution "On the basic level" due to a conflict with the Gaujugendamt It brings the right to punish minors in his care exceeded. Against him then initiated disciplinary proceedings have terminated in November 1942. After a commissioner's representative from early July 1942 Ernst Illing successor Jekelius. Another reason for his call for military service was an intimate relationship with Paula Hitler, sister of Adolf Hitler, whom he met in official contexts. Paula Hitler intervened with Jekelius successfully moved in favor of a friend who was from deportation to the Nazi killing center Hartheim threatened. [4] Another in October 1943 initiated and later recruited disciplinary proceedings to an "improper" reply from Jekelius to the Assistant Secretary of health care. Beginning of 1942 was again called to Jekelius Wehrmacht as a military doctor and was last at a Cossack Division. From August 1943 to November 1943 and from July 1944, he served as chief physician of the neurological unit of the nursing home Lainz, he was also a director post at the mental hospital made the prospect of Rose Hill. Furthermore, he was one of the Viennese "Asozialenkommission" at. Jekelius in 1945 to escape arrest by members of the Red Army and 1948 in Moscow sentenced for their involvement in euthanasia crimes to 25 years hard labor. He died in May 1952 in a Soviet labor camp in bladder cancer. In a Moscow archives were discovered in the summer of 2005, the interrogation logs of Jekelius, in which he charged himself but also under his physician Heinrich Gross difficult. 1941, &quot;after the arrival of Dr. Gross, we started in our clinic with the destruction of children [...] my assistant Dr. Gross had completed a practical course for the killing of children. Every month we killed 6 to 10 children ... Dr. Gross was working under my supervision. The killing of children he adopted on the basis of his experiences before and instructions. After the introduction of Luminal (through the anus) into the body of the child that went right and was about 20-24 hours in this state. Then inevitably death occurred. &quot;In a few cases, so Jekelius, the dose was not enough, Dr. Gross had&quot; injected to achieve the objective in consultation with me, &quot;a lethal cocktail of morphine base. Also confessed during interrogation Jekelius one to have thousands of patients classified according to the documents as a euthanasia case, who were gassed in the Nazi killing centers. Erwin Jekelius, Doctor's Timeline Birth of Erwin Death of Erwin

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请稍后。 Login 电邮: DNA测试 主页Frank Minis Johnson, Jr. (1918 - 1999) Geni requires JavaScript! Please enable JavaScript in your browser's settings to use this part of Geni. or 取消 关注 Frank Minis Johnson, Jr. 0 匹配 0 Research this Person View Frank Minis Johnson, Jr.'s complete profile: See if you are related to Frank Minis Johnson, Jr. Request to view Frank Minis Johnson, Jr.'s family tree View Complete Profile Presidential Medal of Freedom recipients Cover of Time magazine United States Civil Rights Movement 查看全部 直系亲属 Frank Johnson Alabama Johnson About Frank Minis Johnson, Jr. http://en.wikipedia.org/wiki/Frank_Minis_Johnson Frank Minis Johnson, Jr. (October 30, 1918 – July 23, 1999) was a United States Federal judge, made a number of landmark civil rights rulings that helped end segregation in the South. In the words of journalist and historian Bill Moyers, Judge Johnson "altered forever the face of the South." An alumnus of the University of Alabama and the University of Alabama School of Law (one of Johnson's classmates was future Governor George C. Wallace, who would be Johnson's bête noire in the civil rights litigation of the 1960s), Johnson served in the U.S. Army in Europe during World War II, while his wife, Ruth (also a classmate from the University of Alabama) served in the WAVES as an advisor to Hollywood filmmakers. After military service, Johnson entered private law practice in Jasper, Alabama from 1946 to 1953. He was a delegate from Alabama to the 1948 Republican National Convention, and served as a U.S. District Attorney for the Northern District of Alabama, 1953-55. Federal Judicial Service Judge of U.S. District Court for the Middle District of Alabama, 1955&#x2013;1979; Received a recess appointment from President Dwight Eisenhower on October 22, 1955, to a seat vacated by Charles B. Kennamer; nominated on January 12, 1956; Confirmed by the United States Senate on January 31, 1956, and received his commission on February 1, 1956. Served as chief judge, 1966-1979. Service terminated on July 12, 1979, due to his next judicial appointment. Judge of United States Court of Appeals for the Fifth Circuit, 1979&#x2013;1981; Nominated by President Jimmy Carter on April 2, 1979, to a new seat; Confirmed by the Senate on June 19, 1979, and received his commission on June 21, 1979. Service terminated on October 1, 1981, due to assignment to another court. Judge of United States Court of Appeals for the Eleventh Circuit 1981-1999; Reassigned October 1, 1981; Assumed senior status on October 30, 1991. He was succeeded on the bench by Edward Earl Carnes. Service terminated on July 23, 1999, upon his death. [edit] FBI Nomination In 1977 President Carter and Attorney General Griffin Bell asked Johnson to become FBI Director when Director Clarence M. Kelley stepped down. However the day after Carter nominated him, Johnson was found to have an aneurysm, or abnormal swelling, of his abdominal aorta, and later had to withdraw from the nomination. Presidential Medal of Freedom Johnson received the Presidential Medal of Freedom in 1995. Notable Decisions http://en.wikipedia.org/wiki/Frank_Minis_Johnson#Notable_Decisions Frank Johnson, U.S. Federal judge's Timeline Birth of Frank Death of Frank © 2013 Geni.com关于Directory姓氏条款隐私博客维基世界家族树帮助 关注我们成为粉丝

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Published on Georgia DNR - Wildlife Resources Division (http://www.georgiawildlife.com) Fall Alligator Hunting Season Set; Permit Opportunities Increase to 850 SOCIAL CIRCLE, Ga. (5/26/2010) For each of the past eight years, the number of applicants wishing to participate in an alligator quota hunt continues to grow. In 2009, almost 6,000 hunters submitted applications. Beginning this year, 850 applicants will be selected to participate – an increase of 150 permits – in the 2010 alligator hunting season which runs Sept. 4-Oct. 3. “The alligator is a renewable natural resource that scientific data indicates can sustain a regulated harvest on an annual basis,” says WRD Assistant Chief of Game Management John Bowers. “This population stability creates additional flexibility in the areas that can be hunted and the number of animals available for harvest. This has allowed our agency to periodically increase the number of permits available while continuing to ensure the long-term conservation of the alligator population.” Interested hunters must complete and submit a quota hunt application online at www.gohuntgeorgia.com [1] before midnight July 31 (the application period opens June 1, 2010). Hunters receive their selection status by e-mail and those selected get a temporary harvest tag and information packet by mail in early August. All hunters have the opportunity to attend a voluntary training session. During these sessions, wildlife experts provide information on safety, capture and handling techniques, processing and more. Alligators General In Georgia, alligators typically live south of the fall line (which roughly traverses the cities of Columbus, Macon and Augusta), occupying a variety of natural wetland habitats including marshes, swamps, rivers, farm ponds and lakes. Male alligators can reach 16 feet in length, while female alligators rarely surpass 10 feet. Large alligators could weigh more than 800 pounds. Opportunistic carnivores, they eat small mammals, aquatic insects, crayfish, frogs, fish, turtles, water birds and more. For more information on the 2010 alligator hunting season, visit www.gohuntgeorgia.com [1] , contact a WRD Game Management Office or call (770) 760-3045. Georgia Wildlife Resources Division2070 U.S. Hwy. 278, SE, Social Circle, GA 30025 Source URL: http://www.georgiawildlife.com/node/2198 Links:[1] http://www.gohuntgeorgia.com/

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Home > Music > Rock and Pop > Justin Timberlake Tickets Justin Timberlake additional UK tour date Updated:19 November 2013Demand for Justin Timberlake tickets has seen an additional date announced for the UK leg of Justin Timberlake’s 20/20 Experience world tour. London’s The O2 arena will see another performance from Justin Timberlake on 10 April 2014. 20 / 20 Experience UK Tour DatesMarch 2014Sheffield Motorpoint Arena (30) April 2014The O2, London (1, 2, 10) The Hydro, Glasgow (4, 5) Phones 4u Arena, Manchester (7, 8) LG Arena Birmingham (11, 12) The heartthrob made his return to his fans with a performance of his new song 'Suit & Tie' during the 2013 Grammy Awards. The former N' Sync heartthrob was joined on stage by Jay Z. The worldwide popstar released the new album The 20/20 Experience which features 10 tracks, "Pusher Love Girl", "Suit & Tie", "Don't Hold The Wall", "Strawberry Bubblegum", "Tunnel Vision", "Spaceship Coupe", "That Girl", "Let The Groove Get In", “Mirrors" and "Blue Ocean Floor”. Justin Timberlake performed with Jay-Z at the Super Bowl in New Orleans and gave a taster of what to expect on his up-coming shows in the UK and showed that he has become the master of perfection with his slick, executed dance moves and slick performances of "Cry Me a River," "FutureSex/LoveSound," "Rock Your Body," a dreamy "What Comes Around" and the closing "SexyBack," and a special guest appearance by Timbaland.GET ME IN! is Ticketmaster's official market place, the world's largest ticketing company for live events. Buy or sell your Justin Timberlake tickets for all tour dates in a safe and guaranteed way on GET ME IN! Justin Timberlake Tickets - United Kingdom Viewing 1 - 8 (of 8) Sat, 12:02 V Festival 2014 - Weekend Only (No Camping) Tickets Chelmsford Hylands Park Chelmsford 178 Tickets available Sell Tickets Weston Under Lizard Weston Park Staffordshire Weston Under Lizard Sun, 12:03 V Festival 2014 - Sunday (Justin Timberlake) 83 Tickets available Sell V Festival 2014 - Saturday (Justin Timberlake) V Festival 2014 - Weekend Red Camping Tue, 18:30 Justin Timberlake: The 20/20 Experience Tickets London The O2 V Festival 2014 - Weekend Camping V Festival 2014 - Weekend Yellow Camping Justin Timberlake Gossip Justin Timberlake Dangerous BRITS Stunt Planned Justin Timberlake is ready to push the boundaries arrive by speed to the BRIT Awards at the O2 Arena. The super star is later making his way to The Forum for a post-BRITS after show party performance. Read More Gossip Justin Timberlake News April Gig Guide 27 Mar 2014 Justin Timberlake, Gary Barlow, McBusted, Backstreet Boys and Tinie Temaph are just a few of the big names who will be on tour in April. Read full story Justin Timberlake wins big at the Peoples Choice Awards 09 Jan 2014 Justin Timberlake has proved to be the public’s favourite winning three awards at this year’s annual People’s Choice Awards. Read full story Justin Timberlake adds extra UK date 19 Nov 2013 Justin Timberlake has added a further UK date to his 20/20 Experience Tour. Read full story

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Pensyls Mill (inhabited place) Coordinates: Pensyls Mill (preferred,C,V) World (facet) .... North and Central America (continent) (P) ........ United States (nation) (P) ............ Pennsylvania (state) (P) ................ Columbia (county) (P) .................... Pensyls Mill (inhabited place) (P) Place Types: Pensyls Mill.......... [VP Preferred]

2014-15/0000/en_head.json.gz/1263

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» Holiday Gift Baskets » Thanksgiving Gift Baskets Although this tradition is largely recognized in countries such as the United States of American and Canada there's always something to be thankful for. Even though it's origins come from religious purposes in mind we believe it's a secular holiday and everyone should be cheerful every single day. In the old days it was a wonderful time to give thanks for the harvest that had come but today It's a great way to express gratitude & a way to observe everything we have in life. Typical items you'll find in these are fruit, cheese, relaxation products, wine, snacks, and many other delicious treats. These are great for family, friends, and fun gatherings of all kind! Fantastic presents to send out to your loved ones during that special fall holiday are our Thanksgiving presents loaded up to the top with tons of seasonal fall items the whole family can spend time together and enjoy. Not only will it bring the whole family together, everyones taste buds will have a great time jumping with passion! These are simple yet classy baskets we've picked out so you don't have to put them together for yourself manually. We're confident your relatives will certainly feel pleased that you thought of them on Thanksgiving and went the extra mile to send something. Let's face it we live in busy times and not everyone can travel across the country or world for that matter in pursuit of visiting family and friends. Specially if they all live in multiple places. So whether you were able to make it for the holiday or not they are sure to enjoy the treats and lovely products in the baskets as well.

2014-15/0000/en_head.json.gz/1264

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Arsenal target Premier League midfielder Barry linked with Gunners. (©GettyImages). Editor Published9 months ago Arsenal have opened talks with Gareth Barry over a £4million move from Manchester City, according to reports. The Daily Star claims the Gunners are in pole position to land the England international, who has just 12-months left on his current contract at the Etihad Stadium. Barry, who currently earns £100,000 a week at Manchester City, fears he won’t be in the plans of new manager Manuel Pellegrini after featuring regularly under old boss Roberto Mancini. And, with the 2014 World Cup now one season away, the 32-year-old believes he may have to leave the Citizens to be involved with the Three Lions in Brazil, the paper claims. Arsenal boss Arsene Wenger is the favourite to land the player, with the lure of regular first-team football an integral part of the deal at the Emirates Stadium. The report claims the Gunners will offer Barry a 12-month contract on £75,000 a week, with the chance to extend the deal by another year if the stint in north London is a success. Arsenal aren’t the only club interested in Barry, the paper claims, with West Ham United and Tottenham Hotspur also keen. Andre Villas-Boas is eager to build a Spurs side capable of challenging for a place in the Champions League, and the defensive-midfielder would fit nicely into the 4-2-3-1 formation that the Portuguese manager likes to play. And, with Paulinho already joining the club this summer, Tottenham Hotspur have shown they are willing to compete in the transfer market. #Gareth Barry

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Heikki Kovalainen not convinced by Magnussen appointment Many have drawn comparisons between Magnussen & Lewis Hamilton. (©GettyImages). Former McLaren driver Heikki Kovalainen believes the team is taking a major risk that could backfire by giving young Dane Kevin Magnussen a seat for 2014. In a move many are comparing to that of Lewis Hamilton for the 2007 season, the 21-year-old will move up from Formula Renault 3.5, where he was champion this year replacing Sergio Perez. “I’m still surprised by the team’s decision,” the Mexican told Brazil’s Totalrace this week. “I didn’t know the news was coming and, in fact, my contract was already signed. So I was surprised. Asked for his thoughts on how he expects Magnussen to perform, Perez added: “Time will tell if it was the right decision.” Meanwhile the more experienced Kovalainen also expressed his uncertainty as to whether McLaren, who celebrated their 50th anniversary this year, made the right call. “There are two possibilities: Kevin will do well, or he will do badly,” said the 32-year-old, who struggled late in 2013 when he replaced Kimi Raikkonen in the competitive Lotus cockpit. “It is difficult to say which one of the possibilities is the most likely,” added Kovalainen, referring again to Magnussen’s chances. “McLaren seems to really believe in him, but I don’t really know him, other than knowing that he is fast and a good driver,” he continued. Referring back to the comparisons being made between Magnussen’s move and that of Lewis Hamilton, Kovalainen also included Perez’s experience with the team this year which was no where near as successful. “Hamilton was able to fight for the podium from the first race, but in the past season Sergio Perez has not met expectations,” he explained. “They were expecting they could polish the diamond, but it didn’t turn out like that. “In any case, McLaren is a very strong team with excellent facilities and vast resources, so at least in theory they can create the conditions to solve all of a driver’s problems. “There is no guarantee that Magnussen will succeed, but at least he will have a great chance,” added Kovalainen. As for the future of Perez that is looking increasingly likely to be at Force India replacing Paul di Resta and completing an all-new line up alongside Nico Hulkenberg. As the Scot continues a court battle with former manager Anthony Hamilton in London, he was asked by the court about his future in F1. “They (Force India) may be interested, they may not,” Di Resta told the court. “I believe they are in talks with Sergio Perez. It’s looking likely that I will not be driving. “The only team that really has any possibility is Sauber, (but) there has been nothing other than a chat with my manager. “I am speaking to Mercedes-Benz for DTM,” he added.

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NewsLIFE Gives BackEric's JournalCari Blog HomeAbout About L.I.F.E. LIFE in the news Eric's JournalCari Blog More Info on AML Newsletter Our Partners Guestbook Eric's Bucket List TimelineDonate Give to L.I.F.E.Get Help Click here to Apply What We Can Do Freq. Asked Questions L.I.F.E. Gives BackPhotosPhotosL.I.F.E. Around the WorldYouTube ChannelTeam L.I.F.E. Bone Marrow Team About Team L.I.F.E. Meet the Team Race Results Sponsors How to Join Login PhotosL.I.F.E. GearContact Us The Leukemia Ironman Fundraiser for Eric (L.I.F.E.) is a 501(c)(3) non-profit organization dedicated to cancer survivorship by providing assistance to cancer patients in need, scholarship programs, and donating to cancer research laboratories. We will help draw awareness and contribute towards finding more effective treatments, and one day, a cure. About L.I.F.E. If you are between the age of 18 and 30 and currently battling cancer, and would like to apply for financial assistance from L.I.F.E., please click on the Get Help above.The history of life involves a young man from Two Rivers, WI named Eric McLean. On June 23, 2003 he was first diagnosed with Acute Myelogenous Leukemia at just 18 years old. Eric's older brother Mike signed up to compete in the Ironman Wisconsin that fall for him, and his father Brian came up with the monniker Leukemia Ironman Fundraiser for Eric (L.I.F.E.). In a little over a month, $12,000 was raised and donated to the Leukemia and Lymphoma Society for cancer research. After two intense rounds of chemotherapy, Eric achieved remission for the first time and received a stem cell transplant from Mike.Then on December 24, 2007, after 4-1/2 years of being cancer free, the news came that Eric McLean's leukemia had relapsed. So at 23 years old and having just graduated from college, Eric again went through intense chemotherapy treatments and radiation, but this time receiving a stem cell transplant from his younger sister Lindsey. L.I.F.E. made a comeback as Mike again ran in the Ironman Wisconsin on September 7, 2008, and we raised nearly $16,000 for the Leukemia and Lymphoma Society.Eric was cancer free again for nearly a year until June 5, 2009, when his AML relapsed again. Only this time doctors gave him a terminal prognosis, saying it could not be cured. He immediately began a journey to complete his bucket list - a list of things he wanted to accomplish before it was too late: skydiving, driving in a Dodge Viper, gambling in Las Vegas, going to the Caribbean with his family, riding in a hot air balloon, and so much more. It could not have been done without the support and help of many friends, family, and people whom we have never even met. Eric was advised not to treat it, for fear that it would only make him very sick, with the same fatal outcome. He chose to fight it. Just 2 of his 11 doctors agreed to it. They tried a regimen of Decitabine and Mylotarg that had never really been attempted before on a patient as young as Eric. It worked, miraculously, and Eric again achieved remission status.In 2009, L.I.F.E. became its own 501(c)(3) non-profit entity so that it could begin helping other patients directly. Team L.I.F.E. was founded and consists of an entire team of people and athletes dedicated to racing and fundraising for the cause each year.In 2010 after a large fundraising effort, L.I.F.E. and Mike managed a 3rd place finish in the Janus Charity Challenge at the Ironman Wisconsin.Then on January 12, 2011 Eric's bone marrow biopsy returned positive. Facing AML for the 4th time, he was given DLI (donor lymphocyte infusion) from his sister Lindsey to promote GvL effect. The treatment worked and Eric entered remission again on May 4th, 2011. On July 16th 2011, Eric was married to Cari Jaeger in Manitowoc, WI.Then on July 27th, 2011, just one day after Eric and his new wife Cari returned from their honeymoon, they discovered his leukemia had returned. For the next month he remained inpatient at Froedtert Hospital, and after receiving just 1 chemotherapy treatment, he achieved remission status for the 5th time on August 24, 2011. Eric and Cari then moved into their new home in Port Washington, WI. To help ensure a full recovery, Eric again received a 3rd stem cell transplant on November 16, 2011 from an anonymous donor in Europe.Tragically, Eric officially relapsed for the 6th and 7th time on March 7, 2012 - one in his bone marrow, the other in his brain. To combat the 7th relapse, he immediately underwent brain surgery so chemotherapy could be administered directly to his brain. They also gave him a strong dose of radiation. Remission was finally achieved a few months later, as well as a strategic partnership with the LoziLu women's mud run.On August 9th, 2012 Eric's leukemia returned again in the brain as an 8th relapse, or his 9th bout with cancer. This time, however, the disease had taken too much of a toll, and he was sent home on hospice care. Eric tragically passed away just 2 weeks later at the age of 28 on his brother Mike's birthday, August 23, 2012. He posted a final farewell video that went viral to over 1 million viewers and can be seen here.Eric's powerful story of hope and the will to survive has touched us more than words can describe. He has recorded his experiences extensively in his written and video journals, and each one has a positive message that everyone can learn from. It is our mission to continue to support Eric's determination to live, by raising funds to promote cancer survivorship.Thank you so much for all of your love, prayers, and support.-The McLean Family Donate to L.I.F.E. *Tax Deductible Random Photo Two Rivers Relay for Life_7 Quote The reason that these years have been the best is that I think that I might have had a somewhat positive impact on your lives and perhaps your understanding of what cancer is and what it can do, to both those of us that it has personally attacked and those of us who know someone who is going through it. -Eric McLean I just want children to be left with a better life than what I was left with," he said. "I want them to experience the feeling I had in my life when I realized that I really mattered.~ Larry Hisle Realistically, I have two more Olympic cycles in me. I'm not going to let this beat me. I've gained a lot of strength from you guys, if Eric can fight 5 times over I can overcome this one year of setbacks.~ Chris Solinsky Strange is our situation here upon earth. Each of us comes for a short visit, not knowing why, yet sometimes seeming to divine a purpose. From the standpoint of daily life, however, there is one thing we do know: that man is here for the sake of other men. ~ Albert Einstein Never, never, never give up.~ Winston Churchill I have heard there are troubles of more than one kind. Some come from ahead and some come from behind. But I've bought a big bat. I'm all ready you see. Now my troubles are going to have troubles with me! ~ Dr. Seuss Once you choose hope, anything's possible.~ Christopher Reeve If you're going through hell, keep going.~ Winston Churchill Copyright © 2013 L.I.F.E.

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The U.S. government routinely conducts experiments on weather modification By Chris Handy Global Research, October 21, 2007 Daily Texan, University of Texas via U Wire 30 July 2007 Theme: Militarization and WMD, Science and Medicine The U.S. government routinely conducts experiments on weather modification, and has been doing so for at least half a century. Previously classified under such names as “Project Cirrus” (1947) and “Project Popeye” (1966), weather modification is no longer a secret practice. In fact, a bill (S517) was sponsored in 2005 by Texas Sen. Kay Bailey Hutchinson, a Republican, “to establish the Weather Modification Operations and Research Board, and for other purposes.” This bill did not become law. Yet, there is reason to believe that various government institutions are carrying out numerous legal and illegal weather experiments without informing the public. This isn’t just a suspicion of the United States. The Chinese government announced in April the creation of the first-ever artificial snowfall over the city of Nagqu in Tibet. The event was only one in a series of Chinese weather modification experiments that have been going on for years. China, in fact, now conducts more cloud seeding projects than any other nation. Cloud seeding through the use of silver iodide was discovered as a viable way to make rain clouds in 1946. In 1947, the U.S. military attempted to use this method to seed a hurricane, which later hit the Georgia coast near Savannah. In the mid-1960s, similar techniques were used in hopes of muddying the Ho Chi Minh Trail in Vietnam. The idea was to slow enemy troop movements through the introduction of inclement weather, and conversely to prevent foul weather over allies. But cloud seeding with silver iodide is an archaic technique compared with newer advances in nanotechnology and other methods for weather monitoring and control. Microelectric Mechanical Sensors (MEMS) and the newer Global Environmental MEMS Sensors (GEMS), are extremely tiny machines used to monitor weather patterns. No larger than dust particles, the sensors are designed to be sent up inside hurricanes and other weather systems in large numbers, reporting back data as they literally become a part of those systems. This data can later be used to improve weather forecasting and potentially control the weather through a better understanding of the complex mathematics involved in such systems. One goal is to “steer” these systems, sending them to specific targets and increasing or decreasing their size. Another extremely controversial participant in the weather modification game is the infamous HAARP antenna grid in Gakona, Alaska. HAARP, the High Frequency Active Auroral Research Program, is an enormous array of antennas inspired by the free energy experiments of 19th-century electrical playboy Nikola Tesla. Commencing sometime around 1990, HAARP was only recently declassified, and much of the current research there is said to take place in secret. HAARP fires massive amounts of energy into the ionosphere, heating and distorting a section up to 30 miles in diameter. There are various strange and frightening claims made about the project. It may be capable of shifting the position of the jetstream, which could impact global weather in ways that we still do not understand well. Other claims about HAARP, such as that it is part of a massive government mind-control operation or that it forms the main component of a giant death ray, are difficult to verify. But these theories are not as implausible as one might think. Even in the face of mountains of evidence, many people still believe that weather modification of any kind is only a fantasy. People must be aware that these technologies have been around for a long time, are indeed being used and have great potential for dangerous and unethical uses. Our planet’s weather is part of a single interconnected system and any change to it, whether natural or not, affects every other element of that system. The organizations most interested in modifying this system appear to be applying their theories in incredibly irresponsible ways. Chris Handy Related content: Controversial Experimental Weather Modification Bill in US Congress The bill would allow experimental weather modification by artificial methods and implement a national weather modification policy. Experimental weather modification bill – fast tracking – for passage in US Senate and House of Representatives U.S. Senate Bill 517 and U.S. House Bill 2995, a bill that would allow experimental weather modification by artificial methods and implement a national weather modification policy, does not include agriculture or public oversight, is on the “fast track” to… Disclaimer: The contents of this article are of sole responsibility of the author(s). The Centre for Research on Globalization will not be responsible for any inaccurate or incorrect statement in this article. The Center of Research on Globalization grants permission to cross-post original Global Research articles on community internet sites as long as the text & title are not modified. The source and the author's copyright must be displayed. For publication of Global Research articles in print or other forms including commercial internet sites, contact: [email protected] www.globalresearch.ca contains copyrighted material the use of which has not always been specifically authorized by the copyright owner. We are making such material available to our readers under the provisions of "fair use" in an effort to advance a better understanding of political, economic and social issues. The material on this site is distributed without profit to those who have expressed a prior interest in receiving it for research and educational purposes. If you wish to use copyrighted material for purposes other than "fair use" you must request permission from the copyright owner. For media inquiries: [email protected] Copyright © Chris Handy, Daily Texan, University of Texas via U Wire, 2007 Font-size: A+ Global Research Publishers

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(Above image of the Gospel of Thomas courtesy of the Institute for Antiquity and Christianity, Claremont Graduate University) Visit the Bookstore for a complete selection of translations and books about the Gnostic Gospels. The Nag Hammadi Library On the Baptism (B) Translated by John D. Turner [..... from the ] world into the Jordan and from the blindness of the world into the sight of God, from the carnal into the spiritual, from the physical into the angelic, from the created into the Pleroma, from the world into the Aeon, from the servitudes into sonship, from entanglements into one another, from the desert into our village, from the cold into the hot, from [...] into a [...] and we [...] into the [....thus] we were brought from seminal bodies into bodies with a perfect form. Indeed I entered by way of example the remnant for which the Christ rescued us in the fellowship of his Spirit. And he brought us forth who are in him, and from now on the souls will become perfect spirits. Now the things granted us by the first baptism [....invisible ...which] is his, since [.......speak][about...].... Selection made from James M. Robinson, ed., The Nag Hammadi Library, revised edition. HarperCollins, San Francisco, 1990. | Nag Hammadi Library | Gnostic Society Library | Gnosis Archive |

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« Return to roster 2003 Football Roster Kerry Wright Class: r-Jr. Previous School: Tri-Cities HS Hometown: East Point, GA In Record Book: Set a single-season record with 1,280 receiving yards in 2003 ... His 73 receptions in 2003 ranks No. 2 all-time ... Broke the single-season touchdown reception mark with nine in 2003 ... Enters 2004 season ranked eighth all-time in receptions with 91, sixth in receiving yardage (1,541)and tied for 10th in touchdown receptions (11). 2003: A first team All-Sun Belt Conference performer ... Played in all 12 games and started 11 times ... Set a Sun Belt Conference and school record with 1,280 receiving yards ... His 73 receptions ranked as the second most in school history while his nine touchdowns grabs set a new Blue Raider mark ... Also set a new SBC record in receiving yardage per game at 106.7 ... Averaged 6.3 catches and 116.9 yards against Sun Belt competition ... Reeled in eight receptions in the season opener against FAU ... Followed that performance with his first-ever 100-yard receiving game when he registered five grabs for 103 yards against No. 8 Georgia ... Had a career long 71-yard touchdown reception in the fourth quarter against the Bulldogs ... Led the Blue Raiders with four catches at Clemson ... At No. 23 Missouri, Wright hauled in seven receptions for 144 yards and a touchdown to lead all receivers (had a 38-yard acrobatic grab from tailback Eugene Gross) ... Collected five passes for 94 yards vs Temple, including a 71-yard TD pass from Clint Marks ... Also snared a two-point conversion from Marks ... In the win over NMSU, Wright grabbed five passes for a career-best 187 yards (84 yards came after the catch) and a school record tying three touchdowns ... The 187 yards ranked as the third-best effort in school history ... Hauled in a career-high 10 passes for 144 yards against North Texas ... Caught nine passes for 89 yards and a touchdown in the snow at Utah State ... Became the first 1,000-yard receiver in school history when he caught four passes for 97 yards against Troy State ... One of his grabs against TSU was a 56-yard touchdown reception to equal the single-season record ... Ended the season by reeling in eight receptions for 119 yards in a win over Arkansas State. 2002: Competed in all 12 games, including six as a starter ... Hauled in 11 catches for 117 yards and a touchdown ... Set his personal mark with three receptions for 19 yards against North Texas ... Added two catches for 15 yards at Arkansas State ... Had a 53-yard touchdown catch in the win over Louisiana-Lafayette ... Also had four rushing attempts for 60 yards, including a 33-yard run at Kentucky. 2001: Played in all 11 games and earned three starts ... Had seven catches on the season for 144 yards and a touchdown ... His 20.6 yard average per catch was second best on the team ... Led the Blue Raiders in kickoff returns with 16 for 398 yards (24.9 yard average) ... Also had four punt returns for eight yards ... Hauled in a career-best two receptions for 68 yards, including a 58-yard touchdown strike against Idaho ... Registered single catches against Troy State, Ole Miss, New Mexico State, Arkansas State, and LSU ... Had three kickoff returns for 110 yards and a touchdown in the win over Connecticut ... His touchdown return covered 86 yards and marked the longest by a Blue Raider since 1998. 2000: Sat out the season due to NCAA academic requirements ... Practiced the first two weeks of fall camp and had moved all the way up to the top of the depth chart at the "Z" position before having his appeal revoked. High School: Rated a four-star receiver (out of five) and the No. 21 ranked wideout in the nation by Rivals100.com ... Hauled in 58 catches for 1,341 yards and 14 touchdowns as a senior at Tri-Cities ... Voted to Class AAAA All-State team and the All-South Fulton team ... Rated a Super Southern 100 receiver ... Was rated among the top five pass catchers in Georgia by the Atlanta Journal-Constitution ... Selected to play in the prestigious Georgia-Florida All-Star Game. Personal: Guardian: Pam White ... Born: 7/30/81 ... Major: Physical Education. Wright on GoBlueRaiders.com Dec 2, 2003: Five Blue Raiders Named SBC All-Conference; Wright, Westbrook First TeamNov 20, 2003: Blue Raiders Win Season Finale 24-14Nov 15, 2003: Blue Raiders Drop 4OT Game 57-51Nov 13, 2003: Lucky Fan to Win Trip to New Orleans BowlNov 10, 2003: Today's Football Press Conference QuotesNov 9, 2003: MT Holds Off Troy State 27-20 2001 Game-by-Game Stats Choose a game Aug 30, 2001 vs. Vanderbilt Sep 8, 2001 vs. Troy State Sep 22, 2001 vs. Louisiana-Monroe Oct 6, 2001 vs. Idaho Oct 13, 2001 vs. North Texas Oct 20, 2001 vs. Mississippi Oct 27, 2001 vs. New Mexico State Nov 3, 2001 vs. Arkansas State Nov 10, 2001 vs. LSU Nov 17, 2001 vs. Connecticut Aug 31, 2002 vs. Alabama Sep 7, 2002 vs. Tennessee Sep 21, 2002 vs. Kentucky Sep 28, 2002 vs. Southeast Missouri Oct 5, 2002 vs. Arkansas State Oct 12, 2002 vs. Vanderbilt Oct 19, 2002 vs. Louisiana-Lafayette Oct 26, 2002 vs. Idaho Nov 2, 2002 vs. New Mexico State Nov 16, 2002 vs. Louisiana-Monroe Nov 23, 2002 vs. North Texas Nov 30, 2002 vs. Utah State Aug 28, 2003 vs. Florida Atlantic Sep 6, 2003 vs. Georgia Sep 13, 2003 vs. Clemson Sep 20, 2003 vs. Missouri Oct 4, 2003 vs. Temple Nov 1, 2003 vs. Utah State Nov 8, 2003 vs. Troy State Nov 15, 2003 vs. Louisiana-Lafayette Nov 20, 2003 vs. Arkansas State Sep 11, 2004 vs. Akron Sep 18, 2004 vs. Florida Atlantic Sep 25, 2004 vs. Louisiana-Lafayette Oct 2, 2004 vs. North Texas Oct 16, 2004 vs. Florida Oct 30, 2004 vs. Utah State Nov 20, 2004 vs. Troy Football Quick Links Schedule/Notes Cumulative Stats 2013 Football Guide (PDF) Johnny "Red" Floyd Stadium Rick Stockstill Radio Show CoachStockstill.com Football Visiting Team Guide Results/History Archive Only FB

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Women's Cross Country to Race at Southeast Regionals More Information: Week 6 Notes: Jepchirchir Wins Individual Crown Senior Diana Jepchirchir became the eighth different Lady Chanticleer to win the Big South Individual Championship and be named Big South Runner of the Year. For Jepchirchir, this is the second time she’s won an individual conference championship. Prior to attending Coastal, Jepchirchir won the Sun Belt Cross Country Individual title in 2005 while at the University of New Orleans. Running to All-Region Distinction For 12 consecutive seasons, a Coastal runner has garnered All-Region honors. The streak began in 1995 with Catherine Conder receiving her first of three All-Region honors. In that span, Coastal has seen four runners garner multiple All-Region honors in Conder (1995-97), Jolene Williams (1998-2000), Kara Koppel (2001-02) and Anne Marie Moutsinga (2003-05). Making the Top-10 Coastal has placed in the top-10 in the team standings in each of the last three years at the regional meet. The Lady Chanticleers’ highest finish was seventh in 2005 with 234 points, one point ahead of eighth-place finisher James Madison. Just 1K More Saturday’s race will be the third 6K for Coastal this season. At the Brooks Paul Short Run Sept. 28, the Lady Chanticleers averaged a team time of 22:14. Two weeks later at the NCAA Pre-Nationals, Coastal averaged a time of 22:02. Who’s Racing Head coach Alan Connie has entered seniors Aubrey Bergquist and Diana Jepchirchir, junior Felicitas Mensing, sophomore Theresa Schamberger and redshirt freshman Maranie Staab into the Southeast Regional. Additionally, senior Nikki Jasperson and freshman Shelby Donahue are entered as alternates. Among the Ranks The Lady Chants are currently ranked 10th in the latest Southeast Region poll. Coastal has been ranked 10th, which is its highest regional ranking this season, in five of the eight regional polls that were conducted. Throughout the season, Coastal has not been ranked any lower than 12th. Printer-friendly format

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Rocco B. Commisso Soccer Stadium (formerly known as Columbia Soccer Stadium) has been the home venue for Columbia men's soccer since 1984 and the women's squad since 1986. On Saturday, October 12, 2013, the stadium was officially named in honor of Rocco B. Commisso '71SEAS '75BUS in recognition of Commisso’s long-standing contributions to the Lions soccer program, as player and supportive alumnus. The dedication ceremony took place on the field at 5:30 p.m. between the Columbia women's and men’s soccer matches against the University of Pennsylvania “We are thrilled to have named our soccer stadium after Rocco Commisso,” director of intercollegiate athletics and physical education for Columbia Dr. M. Dianne Murphy said in a statement. “Rocco has always been such a wonderful supporter of the University and our soccer program. His generosity means so much to our men and women’s soccer teams – his contributions truly help transform the experiences of the young men and women who compete for Columbia.”Commisso was a member of the 1967 Columbia freshman men’s team that finished undefeated. He also was co-captain of the 1970 varsity men’s squad, the first Columbia soccer team to compete in the NCAA men’s soccer tournament. As an alumnus, he co-founded the alumni advisory group Friends of Columbia Soccer, and served as its Chair from 1979 to 1986. For more than a decade, Columbia has awarded an annual Men’s Soccer Prize in his name.Commisso is the founder, Chairman and CEO of Mediacom Communications Corporation, the nation’s eighth largest cable television company and leading provider of advanced broadband services to 1.3 million customers in 1,500 small cities and towns across America. The venue received an overhaul in June of 2007, when a state-of-the-art FieldTurf playing surface was installed. The surface is a hybrid fiber, rubber and sand infill designed to have a more consistent feel and a faster pace. DIRECTIONS TO BAKER ATHLETICS COMPLEX (Note: Parking for Football games in and around the Baker Athletics Complex is extremely limited. Fans are encouraged to use mass transit when possible.) BY AUTOMOBILE: From WEST SIDE HIGHWAY/HENRY HUDSON PARKWAY: Exit Dyckman Street, and proceed east to Broadway. Make a left on Broadway and proceed 20 blocks north to 218th Street. From FDR/HARLEM RIVER DRIVE: Continue north to end of Harlem River Drive. Bear right at light and proceed north on 10th Avenue to 218th Street. *From MAJOR DEEGAN EXPRESSWAY (I-87): Exit 230th Street. Proceed on 230th Street westbound (from north – make right at light; from south make left at light). Continue on 230th Street to Broadway. Make left on Broadway and proceed 12 blocks to 218th Street. From WEST: Take George Washington Bridge and follow signs for Henry Hudson Parkway North or Major Deegan Expressway North(follow directions above). From NORTH: Take Cross-Westchester Expressway (I-287) or Cross-County Parkway west to Saw Mill River Parkway south. Take the Saw Mill to the Henry Hudson Parkway South or Major Deegan Expressway South (follow directions above). From NEW ENGLAND: Take Connecticut Turnpike (I-95) to Cross Bronx Expressway (I-95). Exit Cross Bronx to Major Deegan Expressway North or Henry Hudson Parkway North (follow directions above). From LONG ISLAND: Take Long Island Expressway East to Clearview Expressway North, or Northern State Parkway/Grand Central Parkway East to Cross Island Parkway North to Throgs Neck Bridge. Bear left after toll for Cross Bronx Expressway (I-95) South (follow directions above). From SOUTH: Take New Jersey Turnpike North to Exit 18 George Washington Bridge (follow directions above). *Commercial and Oversize Vehicles must use Major Deegan Expressway. By MTA NEW YORK CITY SUBWAY: Broadway-Seventh Avenue IRT Local ("1" train) north or south to 215th Street, then walk two blocks north and cross Broadway at W. 218th Street. OR 8th Avenue IND Express ("A" train) north to 207th Street (exit at north end of platform - 211th Street), then proceed north to 218th Street. By MTA METRO-NORTH COMMUTER RAIL: Marble Hill Station is located just across the Harlem River from Baker Athletics Complex, at 225th Street. Walk east to Broadway, then south across the Broadway Bridge to 218th Street. MSOC Hosts Alumni Game April 12 MSOC Spring 2014 Update Najem Signs Professional Contract in Germany MSOC: Attal Selected to Phi Beta Kappa MSOC Places Two on All-Ivy First Team Najem Named Offensive POTY by CSM

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Hansra Tapped To Lead Takes Over from Ashish Bagai July 25, 2011 Fresh off a victory in the ICC America's T20 Championship, Amabhir Jimmy Hansra has been tapped to lead Canada's senior men's team. Cricket Canada confirmed the announcement today in Toronto. Hansra joined the team in 2010 and quickly became an integral member of the side rising to prominence at the 2011 Cricket World Cup finishing second in Canada's run tally. Hansra succeeds Ashish Bagai who stepped aside from full time cricket after the Cricket World Cup. Cricket Canada has also confirmed that they have come to an agreement with Hansra on a full time contract. " I am honoured to be chosen to lead the Cricket Canada Men's National Team. I am aware, excited and focused on all the challenges that lie ahead and will work together with the Management team and the players to further establish cricket in Canada. I would like to thank Ashish Bagai for his contributions as a leader. In a short term under his captaincy, I was impressed by his hard work and professionalism, and will try to continue to build from where he left off. It is an honour to represent your country in any sport or cause, and I will try my best to keep that pride and hunger alive in the heart of every cricketer that puts on the Canadian colours. I thank the organization once again for giving me this opportunity. I will bring my passion, strong work ethic and professionalism into this side as a leader and use it to the best of my ability for the success of the organization." Cricket Canada has a busy month of August with visits from Afghanistan and Trinidad and Tobago. « December Sun Mon Tue Wed Thu Fri Sat 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21December 21, 2012 - 5:00pm ESTOFFICE CLOSED 22December 21, 2012 - 5:00pm ESTOFFICE CLOSED 23December 21, 2012 - 5:00pm ESTOFFICE CLOSED 24December 21, 2012 - 5:00pm ESTOFFICE CLOSED 25December 21, 2012 - 5:00pm ESTOFFICE CLOSED 26December 21, 2012 - 5:00pm ESTOFFICE CLOSED 27December 21, 2012 - 5:00pm ESTOFFICE CLOSED 28December 21, 2012 - 5:00pm ESTOFFICE CLOSED 29December 21, 2012 - 5:00pm ESTOFFICE CLOSED 30December 21, 2012 - 5:00pm ESTOFFICE CLOSEDDecember 30, 2012 - 12:00am CLSTTest Event 31December 21, 2012 - 5:00pm ESTOFFICE CLOSED Provincial Members Cricket Alberta

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Courtesy: Shane Lardinois Kim DeCesare celebrates one of her 16 goals DeCesare to Return to Blue Devils for Senior Season Tuesday 01/31/2013 - Duke Sports Information Print Email RSS Kim DeCesare 2012 Highlights DURHAM, N.C. – Duke women’s soccer head coach Robbie Church announced Thursday that redshirt junior Kim DeCesare will return to Duke for her senior season in the fall of 2013. DeCesare, a sociology and cultural anthropology double major, missed the 2009 season due to a torn right ACL, but is coming off her best collegiate season notching 38 points. “I got hurt my freshman year, so I knew that I wanted to take a fifth year from the time I got to Duke,” DeCesare said. “In high school, I knew that was probably going to be my option. I considered graduating on time and leaving, but that was only if other complications happened or I wasn’t happy, but my plan from the start was to stay.” DeCesare, a native of Massapequa Park, N.Y., tallied 16 goals and six assists last season, including four game winners, and served as a tri-captain for the Blue Devils. As a captain of the team, DeCesare helped lead the Blue Devils to a 15-6-2 overall record and 5-3-2 mark in the ACC, while also making a trip to the NCAA Quarterfinals, where Duke fell to top-seeded Penn State, 1-0. The 5-11 standout has played in 69 career games, while notching 23 goals, nine assists and 55 points. DeCesare was recruited by Church as a defender, but after seeing her goal scoring ability in the 2011 NCAA Tournament, including game winning goals over 24th-ranked Long Beach in the quarterfinals and against Wake Forest in the NCAA College Cup semifinals, Church made the decision to try DeCesare up front in the fall of 2012. That fall, DeCesare made a seamless transition to the forward position and helped the Blue Devils to one of their best offensive seasons in school history, setting school records in points (207) and assists (77), while also posting 65 goals, which is second on the all-time list. Duke concluded the season ranked in the top 10 nationally in the NSCAA rankings for the second straight year, which was a first for the Blue Devils over their 25 years of women’s soccer at Duke. Although DeCesare looks forward to the 2013 season, she will miss the rest of her graduating class – Erin Koballa, Tara Cambell, Maddie Haller, Libby Jandl, Nicole Lipp and Callie Simpkins. “I am super lucky to have come in with that class because those six girls are my best friends, and will likely be my best friends for life,” DeCesare said. “I think that we had the opportunity to kind of change the program and start a new culture for our team, that I am super proud to be a part of. It is sad that I am going to play another season without them, but I am looking forward to working with the girls that I have gotten to know so well throughout the past couple of years. So I am happy to be a part of the upcoming senior class as well, so it is the best of both worlds I guess.” While DeCesare decided to return to Duke, her teammate, Simpkins, who is a redshirt junior, made the difficult decision to move on and accept a position at Goldman Sachs. Simpkins served as an intern at Goldman Sachs in the summer of 2012, and was offered a position upon her graduation in May of 2013. “I definitely considered coming back, it was a battle the entire season about whether I was going to come back or not,” Simpkins said. “I just felt like it was my time to move on. I feel like I am going to thrive in the next chapter of my life, and I am ready to pass the torch down to the junior class. They have done a really good job with this program, and it is their turn to lead and to be on top.” Simpkins, a native of Concord, N.C., served as one of three captains last season, playing in 14 games and notching three goals and two assists, including a goal in the first round of the NCAA Tournament in a 5-0 rout of Loyola-Maryland. Despite missing her freshman season due to a torn ACL in her right knee, Simpkins tallied 62 appearances while recording nine goals and five assists. As a team, Duke will return seven starters in 2013, including the personnel who scored 62-of-65 goals for the Blue Devils in 2012. - duke – Back to Women's Soccer

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Falcons overwhelmed by PacersApril 23, 2009Aiken, SC -- The Pfeiffer Falcon baseball team fell to the No. 7 Pacers of USC-Aiken on Wednesday evening in a non-conference non-playoff game, 28-10. The Falcons are now 26-19-1 overall. The Pacers picked up most of their runs in the game in the bottom of the third inning, posting 15 runs on 15 hits. The 15 hits acquired by the Pacers in the frame tied an NCAA Division II record for most hits in a single inning. The 15 hit-inning ties them with Northern Colorado (2003), North Alabama (1997), South Dakota (1996), St. Francis (1996) and Metro State (1999) for most hits in a single inning. The 15-hit output in the bottom of the third frame also set the Peach Belt Conference record for most hits in a single inning. The Pacers also set the conference record for most hits in a single game at 32. Josh Strickland (Liberty, NC) led the Falcons by going 2-3 at the plate with two runs and two RBI. Myles Pearl (High Point, NC) was 1-2 with one run and four RBI. Chris Grandinetti (Broomfield, CO) led the Pacers at the dish in their win, going 5-for-7 with four runs scored and five RBIs. The Pacers opened the game by making sure that there would never be any question as to the winner, scoring 11 runs in the first two innings to take an 11-0 lead. Pfeiffer, behind a Myles Pearl grand slam in the top half of the third, cut the lead to seven at 11-4, but the Pacers set out upon an uprising like none other before in school history in the bottom of the third to take a stout 26-4 lead. Senior hurler Chris Miller (Atlantic Beach, FL) took the loss for the Falcons, pitching just an inning and a third before being pulled from the game after giving up eight runs and seven hits.� Justin Fry (Augusta, GA) pitched five innings of four-strikeout baseball to record the win for the Pacers on Wednesday evening. Pfeiffer and USC Aiken will conclude their two-game set with a 4 PM contest on Thursday, April 23.

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Francis E. Henry Stadium Home of the Tar Heels On April 24, 1999, the UNC field hockey and women's lacrosse programs dedicated their new home, Francis E. Henry Stadium. The 12,000-square-foot facility, located on Ridge Road, is one of the finest facilities of its kind in the nation. The building houses spacious locker rooms for each sport's players and coaches. In the locker rooms, each player has her own full-length locker, with ample storage space and a plaque bearing her name and number. In the center of the building is a film and meeting room with computers, a big-screen TV and a kitchen area. The team room was updated during the summer of 2009 and is now a "smart classroom," where UNC teams use the latest technology for game and practice preparation, meshing various video and media formats in a wireless environment. The coaches' locker rooms provide another place for reviewing film The building's entranceway houses a sizeable trophy case, which accommodates the Tar Heels' field hockey and lacrosse awards. The stands seat 1,086 fans and also house a concessions stand and restrooms. On the ground level are a sports medicine treatment room and equipment storage areas. Henry Stadium became even more player-friendly in 2008 with the installation of a new AstroTurf surface. As part of the renovation, the crown was removed from the playing field and a top-notch watering system that recycles the field water was added. Francis E. Henry is a UNC graduate who lettered in soccer for the Tar Heels from 1964-66 and now resides in Wilmington, N.C. The facility is named for him and his father, Francis Henry III. Henry Stadium, first-class in every way, could not have been built without contributions from hundreds of Tar Heel supporters. Their generosity is celebrated throughout the stadium, from the engraved bricks out front to plaques on the Carolina blue seats in the stands. Inside are signs recognizing more donors whose gifts made the facility a reality. CAROLINA: The Magazine, April 15 A Blue Carpet Affair Tar Heel Rundown: April 15 2014 Rammy Awards Athletics: SAAC/FAC Meeting

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Review Casolwood Golf Course Golf isn't like other sports where you can take a player out if he's having a bad day. You have to play the whole game. -- Phil Blackmar

2014-15/0000/en_head.json.gz/1278

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1. A composition comprising a tRNA having the nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1, 2, and 3, and the full length complementary polynucleotide sequence that encodes SEQ ID NO: 1, 2 and 3 in a buffer. 2. The composition of claim 1, wherein said tRNA is aminoacylated. 3. The composition of claim 2, wherein said tRNA is aminoacylated with a non-naturally encoded amino acid. 4. The composition of claim 3, wherein said non-naturally encoded amino acid is para-acetylphenylalanine. 5. The composition of claim 2, wherein said tRNA is chemically aminoacylated. 6. The composition of claim 2, wherein said tRNA is enzymatically aminoacylated. 7. The composition of claim 6, wherein said tRNA is enzymatically aminoacylated by an aminoacyl tRNA synthetase. 8. The composition of claim 6, wherein said tRNA is enzymatically aminoacylated by a ribozyme. 9. The composition of claim 1, further comprising an aminoacyl tRNA synthetase, wherein the tRNA is aminoacylated with an amino acid. 10. The composition of claim 9, wherein said amino acid is a non-naturally encoded amino acid. 11. The composition of claim 10, wherein said non-naturally encoded amino acid is para-acetylphenylalanine. 12. The composition of claim 1, wherein the tRNA is derived from an archael tRNA. 13. The composition of claim 1, wherein the tRNA is derived from M. janneschii. 14. The composition of claim 1, further comprising a translation system. 15. The composition of claim 14, wherein said translation system is a cell-free translation system. 16. The composition of claim 14, wherein said translation system is a cell lysate. 17. The composition of claim 14, wherein said translation system is a reconstituted system. 18. The composition of claim 14, wherein said translation system is a cellular translation system. 19. A cell comprising a translation system, wherein the translation system comprises the tRNA of claim 1. 20. The cell of claim 19, wherein the cell is a eukaryotic cell. 21. The cell of claim 20, wherein the eukaryotic cell is a yeast cell. 22. The cell of claim 20, wherein the eukaryotic cell is a fungal cell. 23. The cell of claim 20, wherein the eukaryotic cell is a mammalian cell. 24. The cell of claim 20, wherein the eukaryotic cell is an insect cell. 25. The cell of claim 20, wherein the eukaryotic cell is a plant cell. 26. The cell of claim 19, wherein the cell is a non-eukaryotic cell. 27. The cell of claim 26, wherein the non-eukaryotic cell is an E. coli cell. 28. The cell of claim 19, further comprising a polynucleotide encoding a polypeptide of interest, wherein the polynucleotide comprises a selector codon that is recognized by the tRNA. 29. The cell of claim 28, wherein said polypeptide of interest is human growth hormone. 30. An E. coli cell comprising the tRNA of claim 1. 31. A yeast cell comprising the tRNA of claim 1. 32. A fungal cell comprising a tRNA of claim 1. 33. A mammalian cell comprising a tRNA of claim 1. 34. An insect cell comprising a tRNA of claim 1. 35. A plant cell comprising a tRNA of claim 1. 36. A vector comprising a polynucleotide encoding a tRNA having the nucleic acid sequence selected from the group consisting of SEQ ID NO: 1, 2, and 3, and the full-length complementary polynucleotide sequence that encodes SEQ ID NO: 1, 2 and 3. 37. The vector of claim 36, wherein the vector comprises a plasmid, a cosmid, a phage, or a virus. 38. The vector of claim 36, wherein the vector is an expression vector. 39. A cell comprising the vector of claim 36. 40. A method of producing a polypeptide in a cell with a selected amino acid at a specified position, the method comprising: growing, in an appropriate medium, the cell, where the cell comprises a nucleic acid that comprises at least one selector codon and encodes a polypeptide; and, providing the selected amino acid; wherein the cell further comprises: an orthogonal tRNA (O-tRNA) that functions in the cell and recognizes the selector codon having the amino acid sequence selected from the group consisting of SEQ ID NO: 1, 2, 3, and the full-length complementary polynucleotide sequence that encodes SEQ ID NO: 1, 2 and 3; and, an orthogonal aminoacyl-tRNA synthetase (O-RS), wherein said O-RS aminoacylates the O-tRNA with the selected amino acid. 41. The method of claim 40 wherein said selected amino acid is para-acetyl phenylalanine. 42. The method of claim 40 wherein said polypeptide is human growth hormone. 43. A polynucleotide having a nucleic acid sequence selected from a group consisting of SEQ ID Nos. 1, 2, and 3, and the full-length complementary polynucleotide sequence thereof. CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority to U.S. provisional patent application Ser. No. 60/709,364, filed Aug. 18, 2005, the specification of which is incorporated herein in its entirety. FIELD OF THE PRESENT INVENTION The invention pertains to the field of translation biochemistry. The invention relates to methods for producing and compositions of tRNA and uses thereof. The invention also relates to methods of producing proteins in cells using such tRNA and related compositions. BACKGROUND OF THE PRESENT INVENTION The genetic code of every known organism, from bacteria to humans, encodes the same twenty common amino acids. Different combinations of the same twenty natural amino acids form proteins that carry out virtually all the complex processes of life, from photosynthesis to signal transduction and the immune response. In order to study and modify protein structure and function, scientists have attempted to manipulate both the genetic code and the amino acid sequence of protein. However, it has been difficult to remove the constraints imposed by the genetic code that limit proteins to twenty genetically encoded standard building blocks (with the rare exception of selenocysteine (see, e.g., A. Bock et al., (1991), Molecular Microbiology 5:515-20) and pyrrolysine (see, e.g., G. Srinivasan, et al., (2002), Science 296:1459-62). Some progress has been made to remove these constraints, although this progress has been limited and the ability to rationally control protein structure and function is still in its infancy. For example, chemists have developed methods and strategies to synthesize and manipulate the structures of small molecules (see, e.g., E. J. Corey, & X.-M. Cheng, The Logic of Chemical Synthesis (Wiley-Interscience, New York, 1995)). Total synthesis (see, e.g., B. Merrifield, (1986), Science 232:341-7 (1986)), and semi-synthetic methodologies (see, e.g., D. Y. Jackson et al., (1994) Science 266:243-7; and, P. E. Dawson, & S. B. Kent, (2000), Annual Review of Biochemistry 69:923-60), have made it possible to synthesize peptides and small proteins, but these methodologies have limited utility with proteins over 10 kilo Daltons (kDa). Mutagenesis methods, though powerful, are restricted to a limited number of structural changes. In a number of cases, it has been possible to competitively incorporate close structural analogues of common amino acids throughout proteins. See, e.g., R. Furter, (1998), Protein Science 7:419-26; K. Kirshenbaum, et al., (2002), ChemBioChem 3:235-7; and, V. Doring et al., (2001), Science 292:501-4. Chemical peptide ligation and native chemical ligation are described in U.S. Pat. No. 6,184,344, U.S. Patent Publication No. 2004/0138412, U.S. Patent Publication No. 2003/0208046, WO 02/098902, and WO 03/042235, which are incorporated by reference herein. Lu et al. in Mol. Cell. 2001 Oct.; 8(4):759-69 describe a method in which a protein is chemically ligated to a synthetic peptide containing unnatural amino acids (expressed protein ligation). Early work demonstrated that the translational machinery of E. coli would accommodate amino acids similar in structure to the common twenty. See, Hortin, G., and Boime, I. (1983) Methods Enzymol. 96:777-784. This work was further extended by relaxing the specificity of endogenous E. coli synthetases so that they activate unnatural amino acids as well as their cognate natural amino acid. Moreover, it was shown that mutations in editing domains could also be used to extend the substrate scope of the endogenous synthetase. See, Doring, V., et al., (2001) Science 292:501-504. However, these strategies are limited to recoding the genetic code rather than expanding the genetic code and lead to varying degrees of substitution of one of the common twenty amino acids with an unnatural amino acid. Later it was shown that unnatural amino acids could be site-specifically incorporated into proteins in vitro by the addition of chemically aminoacylated orthogonal amber suppressor tRNA's to an in vitro transcription/translation reaction. See, e.g., Noren, C. J., et al. (1989) Science 244:182-188; Bain, J. D., et al., (1989) J. Am. Chem. Soc. 111:8013-8014; Dougherty, D. A. (2000) Curr. Opin. Chem. Biol. 4, 645-652; Cornish, V. W., et al. (1995) Angew. Chem., Int. Ed. 34:621-633; J. A. Ellman, et al., (1992), Science 255:197-200; and, D. Mendel, et al., (1995), Annual Review of Biophysics and Biomolecular Structure 24:435-462. These studies show that the ribosome and translation factors are compatible with a large number of unnatural amino acids, even those with unusual structures. Unfortunately, the chemical aminoacylation of tRNA's is difficult, and the stoichiometric nature of this process severely limited the amount of protein that could be generated. Unnatural amino acids have been microinjected into cells. For example, unnatural amino acids were introduced into the nicotinic acetylcholine receptor in Xenopus oocytes (e.g., M. W. Nowak, et al. (1998), In vivo incorporation of unnatural amino acids into ion channels in Xenopus oocyte expression system, Method Enzymol. 293:504-529) by microinjection of a chemically misacylated Tetrahymena thermophila tRNA (e.g., M. E. Saks, et al. (1996), An engineered Tetrahymena tRNAGln for in vivo incorporation of unnatural amino acids into proteins by nonsense suppression, J. Biol. Chem. 271:23169-23175), and the relevant mRNA. See, also, D. A. Dougherty (2000), Unnatural amino acids as probes of protein structure and function, Curr. Opin. Chem. Biol. 4:645-652 and M. W. Nowak, P. C. Kearney, J. R. Sampson, M. E. Saks, C. G. Labarca, S. K. Silverman, W. G. Zhong, J. Thorson, J. N. Abelson, N. Davidson, P. G. Schultz, D. A. Dougherty and H. A. Lester, Science, 268:439 (1995). A Xenopus oocyte was coinjected with two RNA species made in vitro: an mRNA encoding the target protein with a UAG stop codon at the amino acid position of interest and an amber suppressor tRNA aminoacylated with the desired unnatural amino acid. The translational machinery of the oocyte then inserts the unnatural amino acid at the position specified by UAG. Unfortunately, this methodology is limited to proteins in cells that can be microinjected, and because the relevant tRNA is chemically acylated in vitro, and cannot be re-acylated, the yields of protein are very low. To overcome these limitations, new components, e.g., orthogonal tRNA's, orthogonal aminoacyl-tRNA synthetases and pairs thereof, were added to the protein biosynthetic machinery of the prokaryote Escherichia coli (E. coli) (see e.g., L. Wang, et al., (2001), Science 292:498-500) and the eukaryote Sacchromyces cerevisiae (S. cerevisiae) (e.g., J. Chin et al., Science 301:964-7 (2003)) which has enabled the incorporation of non-genetically encoded amino acids to proteins in vivo. A number of new amino acids with novel chemical, physical or biological properties, including photoaffinity labels and photoisomerizable amino acids, photocrosslinking amino acids (see, e.g., Chin, J. W., et al. (2002) Proc. Natl. Acad. Sci. U.S.A. 99:11020-11024; and, Chin, J. W., et al., (2002) J. Am. Chem. Soc. 124:9026-9027), keto amino acids (see, e.g., Wang, L., et al., (2003) Proc. Natl. Acad. Sci. U.S.A. 100:56-61 and Zhang, Z. et al., Biochem. 42(22):6735-6746 (2003)), heavy atom containing amino acids, and glycosylated amino acids have been incorporated efficiently and with high fidelity into proteins in E. coli and in yeast in response to, e.g., the amber codon (TAG), using this methodology. See, e.g., J. W. Chin, & P. G. Schultz, (2002), ChemBioChem 3(11):1135-1137 and, L. Wang, & P. G. Schultz, (2002), Chem. Comm., 1:1-11. Several other orthogonal pairs have been reported. Glutaminyl (see, e.g., Liu, D. R., and Schultz, P. G. (1999) Proc. Natl. Acad. Sci. U.S.A. 96:4780-4785), aspartyl (see, e.g., Pastrnak, M., et al., (2000) Helv. Chim. Acta 83:2277-2286), and tyrosyl (see, e.g., Ohno, S., et al., (1998) J. Biochem. (Tokyo, Jpn.) 124:1065-1068; and, Kowal, A. K., et al., (2001) Proc. Natl. Acad. Sci. U.S.A. 98:2268-2273) systems derived from S. cerevisiae tRNA's and synthetases have been described for the potential incorporation of unnatural amino acids in E. coli. Systems derived from the E. coli glutaminyl (see, e.g., Kowal, A. K., et al., (2001) Proc. Natl. Acad. Sci. U.S.A. 98:2268-2273) and tyrosyl (see, e.g., Edwards, H., and Schimmel, P. (1990) Mol. Cell. Biol. 10:1633-1641) synthetases have been described for use in S. cerevisiae. The E. coli tyrosyl system has been used for the incorporation of 3-iodo-L-tyrosine in vivo, in mammalian cells. See, Sakamoto, K., et al., (2002) Nucleic Acids Res. 30:4692-4699. Typically, these systems have made use of the amber stop codon. To further expand the genetic code, there is a need to develop improved and/or additional components of the biosynthetic machinery, e.g., tRNA's. This invention fulfills these and other needs, as will be apparent upon review of the following disclosure. SUMMARY OF THE PRESENT INVENTION To expand the genetic code, the invention provides compositions of and methods of producing orthogonal tRNA's. Aminoacyl-tRNA synthetases aminoacylate tRNA's of the present invention with a non-naturally encoded amino acid. These translational components can be used to incorporate a selected amino acid in a specific position in a growing polypeptide chain (during nucleic acid translation) in response to a selector codon that is recognized by the tRNA. Methods of producing a protein in a cell with a selected amino acid at a specified position are also a feature of the present invention. For example, a method includes growing, in an appropriate medium, a cell, where the cell comprises a nucleic acid that comprises at least one selector codon and encodes a protein; and, providing the selected amino acid. The cell further comprises: an orthogonal tRNA (O-tRNA) that functions in the cell and recognizes the selector codon; and, an orthogonal aminoacyl-tRNA synthetase (O-RS) that preferentially aminoacylates the O-tRNA with the selected amino acid. Typically, the O-tRNA comprises suppression activity in the presence of a cognate synthetase. A protein produced by this method is also a feature of the present invention. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1�The cloverleaf structure of J17 tRNA (SEQ ID NO.: 8) with TψC mutation sites is shown. FIG. 2�Supression of an amber mutation in human growth hormone is shown using J17 or J17 mutants (F12, F13, F14). Total cell lysate for each sample was analyzed by SDS PAGE. FIG. 3�Supression of an amber mutation in human growth hormone is shown in different cell lines using F13. DEFINITIONS Before describing the invention in detail, it is to be understood that this invention is not limited to particular biological systems, which can, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention, which will be limited only by the appended claims. As used herein and in the appended claims, the singular forms �a�, �an� and �the� include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to �a cell� includes a combination of two or more cells and includes equivalents thereof known to those of ordinary skill in the art, and so forth. Reference to �bacteria� includes mixtures of bacteria, and the like. Unless defined herein and below in the reminder of the specification, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the invention pertains. All publications and patents mentioned herein are incorporated herein by reference for the purpose of describing and disclosing, for example, the constructs and methodologies that are described in the publications, which might be used in connection with the presently described invention. The publications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the inventors are not entitled to antedate such disclosure by virtue of prior invention or for any other reason. Homologous: Proteins and/or protein sequences are �homologous� when they are derived, naturally or artificially, from a common ancestral protein or protein sequence. Similarly, nucleic acids and/or nucleic acid sequences are homologous when they are derived, naturally or artificially, from a common ancestral nucleic acid or nucleic acid sequence. For example, any naturally occurring nucleic acid can be modified by any available mutagenesis method to include one or more selector codon. When expressed, this mutagenized nucleic acid encodes a polypeptide comprising one or more selected amino acid, e.g. unnatural amino acid. The mutation process can, of course, additionally alter one or more standard codon, thereby changing one or more standard amino acid in the resulting mutant protein as well. The one or more standard amino acid may be changed to an unnatural amino acid or a natural amino acid. Homology is generally inferred from sequence similarity between two or more nucleic acids or proteins (or sequences thereof). The precise percentage of similarity between sequences that is useful in establishing homology varies with the nucleic acid and protein at issue, but as little as 25% sequence similarity is routinely used to establish homology. Higher levels of sequence similarity, e.g., 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% or more, can also be used to establish homology. Methods for determining sequence similarity percentages (e.g., BLASTP and BLASTN using default parameters) are described herein and are generally available. Orthogonal: As used herein, the term �orthogonal� refers to a molecule (e.g., an orthogonal tRNA (O-tRNA) and/or an orthogonal aminoacyl tRNA synthetase (O-RS)) that is used with reduced efficiency by a system of interest (e.g., a translational system, e.g., a cell). Orthogonal refers to the inability or reduced efficiency, e.g., less than 20% efficient, less than 10% efficient, less than 5% efficient, or e.g., less than 1% efficient, of an orthogonal tRNA and/or orthogonal RS to function in the translation system of interest. For example, an orthogonal tRNA in a translation system of interest is aminoacylated by any endogenous RS of a translation system of interest with reduced or even zero efficiency, when compared to aminoacylation of an endogenous tRNA by an endogenous RS. In another example, an orthogonal RS aminoacylates any endogenous tRNA in the translation system of interest with reduced or even zero efficiency, as compared to aminoacylation of the endogenous tRNA by an endogenous RS. A second orthogonal molecule can be introduced into the cell that functions with the first orthogonal molecule. For example, an orthogonal tRNA/RS pair includes introduced complementary components that function together in the cell with an efficiency (e.g., about 50% efficiency, about 60% efficiency, about 70% efficiency, about 75% efficiency, about 80% efficiency, about 85% efficiency, about 90% efficiency, about 95% efficiency, or about 99% or more efficiency) to that of a corresponding tRNA/RS endogenous pair. �Improvement in orthogonality� refers to enhanced orthogonality compared to a starting material or a naturally occurring tRNA or RS. Cognate: The term �cognate� refers to components that function together, e.g., a tRNA and an aminoacyl-tRNA synthetase. The components can also be referred to as being complementary. Preferentially aminoacylates: The term �preferentially aminoacylates� refers to an efficiency, e.g., about 70% efficient, about 75% efficient, about 80% efficient, about 85% efficient, about 90% efficient, about 95% efficient, or about 99% or more efficient, at which an O-RS aminoacylates an O-tRNA with a selected amino acid, e.g., an unnatural amino acid, compared to the O-RS aminoacylating a naturally occurring tRNA or a starting material used to generate the O-tRNA. The unnatural amino acid is then incorporated into a growing polypeptide chain with high fidelity, e.g., at greater than about 70% efficiency for a given selector codon, at greater than about 75% efficiency for a given selector codon, at greater than about 80% efficiency for a given selector codon, at greater than about 85% efficiency for a given selector codon, at greater than about 90% efficiency for a given selector codon, greater than about 95% efficiency for a given selector codon, or greater than about 99% efficiency for a given selector codon. Selector codon: The term �selector codon� refers to codons recognized by the O-tRNA in the translation process and not recognized by an endogenous tRNA. The O-tRNA anticodon loop recognizes the selector codon on the mRNA and incorporates its amino acid, e.g., a selected amino acid, such as an unnatural amino acid, at this site in the polypeptide. Selector codons can include but are not limited to, e.g., nonsense codons, such as, stop codons, including but not limited to, amber, ochre, and opal codons; four or more base codons; rare codons; codons derived from natural or unnatural base pairs and/or the like. For a given system, a selector codon can also include one of the natural three base codons, wherein the endogenous system does not use (or rarely uses) said natural three base codon. For example, this includes a system that is lacking a tRNA that recognizes the natural three base codon, and/or a system wherein the natural three base codon is a rare codon. Suppressor tRNA: A suppressor tRNA is a tRNA that alters the reading of a messenger RNA (mRNA) in a given translation system, e.g., by providing a mechanism for incorporating an amino acid into a polypeptide chain in response to a selector codon. For example, a suppressor tRNA can read through a codon including but not limited to, a stop codon, a four base codon, or a rare codon. Suppression activity: The term �suppression activity� refers to the ability of a tRNA, e.g., a suppressor tRNA, to read through a selector codon. Activity can be expressed as a percentage of activity observed as compared to a control (e.g., lacking a cognate synthetase). Translation system: The term �translation system� refers to the components necessary to incorporate a naturally occurring amino acid into a growing polypeptide chain (protein). Components of a translation system can include, e.g., ribosomes, tRNA's, synthetases, mRNA and the like. The components of the present invention can be added to an in vitro or in vivo translation system. Examples of translation systems include but are not limited to, a non-eukaryotic cell, e.g., a bacterium (such as E. coli), a eukaryotic cell, e.g., a yeast cell, a mammalian cell, a plant cell, an algae cell, a fungus cell, an insect cell, a cell-free translational system e.g., a cell lysate, and/or the like. Translation systems may be cellular or cell-free, and may be prokaryotic or eukaryotic. Cellular translation systems include, but are not limited to, whole cell preparations such as permeabilized cells or cell cultures wherein a desired nucleic acid sequence can be transcribed to mRNA and the mRNA translated. Cell-free translation systems are commercially available and many different types and systems are well-known. Examples of cell-free systems include, but are not limited to, prokaryotic lysates such as Escherichia coli lysates, and eukaryotic lysates such as wheat germ extracts, insect cell lysates, rabbit reticulocyte lysates, rabbit oocyte lysates and human cell lysates. Eukaryotic extracts or lysates may be preferred when the resulting protein is glycosylated, phosphorylated or otherwise modified because many such modifications are only possible in eukaryotic systems. Some of these extracts and lysates are available commercially (Promega; Madison, Wis.; Stratagene; La Jolla, Calif.; Amersham; Arlington Heights, Ill.; GIBCO/BRL; Grand Island, N.Y.). Membranous extracts, such as the canine pancreatic extracts containing microsomal membranes, are also available which are useful for translating secretory proteins. Reconstituted translation systems may also be used. Mixtures of purified translation factors have also been used successfully to translate mRNA into protein as well as combinations of lysates or lysates supplemented with purified translation factors such as initiation factor-1 (IF-1), IF-2, IF-3 (α or β), elongation factor T (EF-Tu), or termination factors. Cell-free systems may also be coupled transcription/translation systems wherein DNA is introduced to the system, transcribed into mRNA and the mRNA translated as described in Current Protocols in Molecular Biology (F. M. Ausubel et al. editors, Wiley Interscience, 1993), which is hereby specifically incorporated by reference. RNA transcribed in eukaryotic transcription system may be in the form of heteronuclear RNA (hnRNA) or 5′-end caps (7-methyl guanosine) and 3′-end poly A tailed mature mRNA, which can be an advantage in certain translation systems. For example, capped mRNAs are translated with high efficiency in the reticulocyte lysate system. Selected amino acid: The term �selected amino acid� refers to any desired naturally occurring amino acid or unnatural amino acid. As used herein, the term �unnatural amino acid� or �non-naturally encoded amino acid� refers to any amino acid, modified amino acid, and/or amino acid analogue that is not one of the 20 common naturally occurring amino acids or selenocysteine or pyrrolysine. Other terms that may be used synonymously with the term �non-naturally encoded amino acid� and �unnatural amino acid� are �non-natural amino acid,� �non-naturally-occurring amino acid,� and variously hyphenated and non-hyphenated versions thereof. The term �non-naturally encoded amino acid� also includes, but is not limited to, amino acids that occur by modification (e.g. post-translational modifications) of a naturally encoded amino acid (including but not limited to, the 20 common amino acids or pyrrolysine and selenocysteine) but are not themselves naturally incorporated into a growing polypeptide chain by the translation complex. Examples of such non-naturally-occurring amino acids include, but are not limited to, N-acetylglucosaminyl-L-serine, N-acetylglucosaminyl-L-threonine, and O-phosphotyrosine. Derived from: As used herein, the term �derived from� refers to a component that is isolated from or made using information from a specified molecule or organism. Positive selection or screening marker: As used herein, the term �positive selection or screening marker� refers to a marker that when present, e.g., expressed, activated or the like, results in identification of a cell with the positive selection marker from those without the positive selection marker. Negative selection or screening marker: As used herein, the term �negative selection or screening marker� refers to a marker that when present, e.g., expressed, activated or the like, allows identification of a cell that does not possess the desired property (e.g., as compared to a cell that does possess the desired property). Reporter: As used herein, the term �reporter� refers to a component that can be used to select target components of a system of interest. For example, a reporter can include a protein, e.g., an enzyme, that confers antibiotic resistance or sensitivity (including, but not limited to, β-lactamase, chloramphenicol acetyltransferase (CAT), and the like), a fluorescent screening marker (including, but not limited to, green fluorescent protein (e.g., GFP), YFP, EGFP, RFP, a luminescent marker (including but not limited to, a firefly luciferase protein), an affinity based screening marker, or positive or negative selectable marker genes such as lacZ, β-gal/lacZ (β-galactosidase), ADH (alcohol dehydrogenase), his3, ura3, leu2, lys2, or the like. Eukaryote: As used herein, the term �eukaryote� refers to organisms belonging to the phylogenetic domain Eucarya such as animals (including but not limited to, mammals, insects, reptiles, birds, etc.), ciliates, plants (including but not limited to, monocots, dicots, algae, etc.), fungi, yeasts, flagellates, microsporidia, protists, etc. Non-eukaryote: As used herein, the term �non-eukaryote� refers to non-eukaryotic organisms. For example, a non-eukaryotic organism can belong to the Eubacteria (including but not limited to, Escherichia coli, Thermus thermophilus, Bacillus stearothermophilus, Pseudomonas fluorescens, Pseudomonas aeruginosa, Pseudomonas putida, etc.) phylogenetic domain, or the Archaea (e.g., Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Halobacterium such as Haloferax volcanii and Halobacterium species NRC-1, Archaeoglobus fulgidus, Pyrococcus furiosus, Pyrococcus horikoshii, Aeuropyrum pernix, etc.) phylogenetic domain. Conservative variant: The term �conservative variant� refers to a translation component, e.g., a conservative variant O-tRNA or a conservative variant O-RS, that functionally performs like the component from which the conservative variant is based, e.g., an O-tRNA or O-RS, but has variations in the sequence. For example, an O-RS will aminoacylate a complementary O-tRNA or a conservative variant O-tRNA with a selected amino acid, e.g., an unnatural amino acid, although the O-tRNA and the conservative variant O-tRNA do not have the same sequence. Similarly, a tRNA will be aminoacylated with a selected amino acid, e.g., an unnatural amino acid, by a complementary O-RS or a conservative variant O-RS, although the O-RS and the conservative variant O-RS do not have the same sequence. The conservative variant can have, e.g., one variation, two variations, three variations, four variations, or five or more variations in sequence, as long as the conservative variant is complementary to the corresponding O-tRNA or O-RS. Selection or screening agent: As used herein, the term �selection or screening agent� refers to an agent that, when present, allows for a selection/screening of certain components from a population. For example, a selection or screening agent includes, but is not limited to, e.g., a nutrient, an antibiotic, a wavelength of light, an antibody, an expressed polynucleotide, or the like. The selection agent can be varied, e.g., by concentration, intensity, etc. The term �not efficiently recognized� refers to an efficiency, e.g., less than about 10%, less than about 5%, or less than about 1%, at which a RS from one organism aminoacylates O-tRNA. DETAILED DESCRIPTION Translation systems that are suitable for making proteins that include one or more selected amino acids, e.g., an unnatural amino acid, are described in U.S. patent application Ser. Nos. 10/126,931, entitled �METHODS AND COMPOSITION FOR THE PRODUCTION OF ORTHOGONAL tRNA-AMINOACYL tRNA SYNTHETASE PAIRS� and 10/126,927, entitled �IN VIVO INCORPORATION OF UNNATURAL AMINO ACIDS.� In addition, see U.S. Ser. No. 10/825,867 entitled �EXPANDING THE EUKARYOTIC GENETIC CODE.� Each of these applications is incorporated herein by reference in its entirety. Such translation systems generally comprise cells that include an orthogonal tRNA (O-tRNA), an orthogonal aminoacyl tRNA synthetase (O-RS), and a selected amino acid, e.g., an unnatural amino acid, where the O-RS aminoacylates the O-tRNA with the selected amino acid. An orthogonal pair of the present invention is composed of an O-tRNA, e.g., a suppressor tRNA, a frameshift tRNA, or the like, and an O-RS. The O-tRNA recognizes a first selector codon and has suppression activity in presence of a cognate synthetase in response to a selector codon. The cell uses the components to incorporate the selected amino acid into a growing polypeptide chain. For example, a nucleic acid that comprises a polynucleotide that encodes a polypeptide of interest can also be present, where the polynucleotide comprises a selector codon that is recognized by the O-tRNA. The translation system can also be an in vitro system. tRNA molecules of the present invention are useful in any translational system, including systems that utilize ribosomes in translation. The translation system may also be a cell-free (in-vitro) translational system. In these systems, which can include either mRNA as a template (in-vitro translation) or DNA as a template (combined in-vitro transcription and translation), the in vitro synthesis is directed by the ribosomes. Considerable effort has been applied to the development of cell-free protein expression systems. See, e.g., Kim, D. M. and J. R. Swartz, Biotechnology and Bioengineering, 74:309-316 (2001); Kim, D. M. and J. R. Swartz, Biotechnology Letters, 22, 1537-1542, (2000); Kim, D. M., and J. R. Swartz, Biotechnology Progress, 16, 385-390, (2000); Kim, D. M., and J. R. Swartz, Biotechnology and Bioengineering, 66, 180-188, (1999); and Patnaik, R. and J. R. Swartz, Biotechniques 24, 862-868, (1998); U.S. Pat. No. 6,337,191; U.S. Patent Publication No. 2002/0081660; WO 00/55353; WO 90/05785, which are incorporated by reference herein. Another approach that may be applied includes the mRNA-peptide fusion technique. See, e.g., R. Roberts and J. Szostak, Proc. Natl. Acad. Sci. (USA) 94:12297-12302 (1997); A. Frankel, et al., Chemistry & Biology 10:1043-1050 (2003). In this approach, an mRNA template linked to puromycin is translated into peptide on the ribosome. If one or more tRNA molecules have been modified, non-natural amino acids can be incorporated into the peptide as well. After the last mRNA codon has been read, puromycin captures the C-terminus of the peptide. If the resulting mRNA-peptide conjugate is found to have interesting properties in an in vitro assay, its identity can be easily revealed from the mRNA sequence. In this way, one may screen libraries of polypeptides comprising one or more non-naturally encoded amino acids to identify polypeptides having desired properties. More recently, in vitro ribosome translations with purified components have been reported that permit the synthesis of peptides substituted with non-naturally encoded amino acids. See, e.g., A. Forster et al., Proc. Natl. Acad. Sci. (USA) 100:6353 (2003). In certain embodiments, an E. coli cell comprising the tRNA of the present invention includes such a translation system. For example, the E. coli cell of the present invention includes an orthogonal tRNA (O-tRNA), where the O-tRNA comprises suppression activity in presence of a cognate synthetase in response to a selector codon; an orthogonal aminoacyl-tRNA synthetase (O-RS); a selected amino acid; and, a nucleic acid that comprises a polynucleotide that encodes a polypeptide of interest, where the polynucleotide comprises a selector codon that is recognized by the O-tRNA. The invention also features multiple O-tRNA/O-RS pairs in a cell, which allows incorporation of more than one selected amino acid. In certain embodiments, the cell can further include an additional different O-tRNA/O-RS pair and a second selected amino acid, where the O-tRNA recognizes a second selector codon and the O-RS preferentially aminoacylates the O-tRNA with the second selected amino acid. For example, a cell can further comprise, e.g., an amber suppressor tRNA-aminoacyl tRNA synthetase pair derived from the tyrosyl-tRNA synthetase of Methanococcus jannaschii. The O-tRNA and/or the O-RS can be naturally occurring or can be derived by mutation of a naturally occurring tRNA and/or RS, e.g., which generates libraries of tRNA's and/or libraries of RSs, from a variety of organisms. For example, one strategy of producing an orthogonal tRNA/aminoacyl-tRNA synthetase pair involves importing a heterologous tRNA/synthetase pair from, e.g., a source other than the host cell, or multiple sources, into the host cell. The properties of the heterologous synthetase candidate include, e.g., that it does not charge any host cell tRNA, and the properties of the heterologous tRNA candidate include, e.g., that it is not aminoacylated by any host cell synthetase. In addition, the heterologous tRNA is orthogonal to all host cell synthetases. A second strategy for generating an orthogonal pair involves generating mutant libraries from which to screen and/or select an O-tRNA or O-RS. These strategies can also be combined. In various embodiments, the O-tRNA and O-RS are derived from at least one organism. In another embodiment, the O-tRNA is derived from a naturally occurring or mutated naturally occurring tRNA from a first organism and the O-RS is derived from naturally occurring or mutated naturally occurring RS from a second organism. In one embodiment, the first and second organisms are different. For example, an orthogonal pair may include a tRNA synthetase derived from Methanobacterium thermoautotrophicum, and a tRNA derived from an archael tRNA (e.g., from Halobacterium sp. NRC-1). Alternatively, the first and second organisms are the same. See the section entitled �Sources and Host Organisms� herein for additional information. In certain embodiments of the present invention, an O-tRNA of the present invention comprises or is encoded by a polynucleotide sequence as set forth in SEQ ID NO.: 1, 2, or 3, or a complementary polynucleotide sequence thereof, or a conservative variation thereof. See also the section entitled �Nucleic Acid and Polypeptide Sequence and Variants� herein. Orthogonal tRNA (O-tRNA) An orthogonal tRNA (O-tRNA) mediates incorporation of a selected amino acid into a protein that is encoded by a polynucleotide that comprises a selector codon that is recognized by the O-tRNA, e.g., in vivo or in vitro. An O-tRNA of the present invention may be aminoacylated with a desired amino acid by any method or technique, including but not limited to, chemical or enzymatic aminoacylation. The aminoacylated O-tRNA of the present invention may be added directly to a translation system. An O-tRNA of the present invention may be aminoacylated by an RS with a selected amino acid in vitro or in vivo. In addition, the RS may be an O-RS. An O-tRNA of the present invention can be provided to the translation system (e.g., in vitro translation components, or a cell) directly, or by providing a polynucleotide that encodes an O-tRNA or a portion thereof. For example, an O-tRNA, or a portion thereof, is encoded by a polynucleotide sequence as set forth in SEQ ID NO.: 1, 2, 3, or a complementary polynucleotide sequence thereof, or a conservative variation thereof. An O-tRNA of the present invention comprises suppression activity in the presence of a cognate synthetase in response to a selector codon. Suppression activity can be determined by any of a number of assays known in the art. For example, a β-galactosidase reporter assay can be used. A derivative of a plasmid that expresses lacZ gene under the control of promoter is used, e.g., where the Leu-25 of the peptide VVLQRRDWEN of lacZ is replaced by a selector codon, e.g., TAG, TGA, AGGA, etc. codons, or sense codons (as a control) for tyrosine, serine, leucine, etc. The derivatived lacZ plasmid is introduced into cells from an appropriate organism (e.g., an organism where the orthogonal components can be used) along with plasmid comprising an O-tRNA of the present invention. A cognate synthetase can also be introduced (either as a polypeptide or a polynucleotide that encodes the cognate synthetase when expressed). The cells are grown in media to a desired density, e.g., to an OD600 of about 0.5., and β-galactosidase assays are performed, e.g., using the BetaFluor� β-Galactosidase Assay Kit (Novagen). Percent suppression is calculated as the percentage of activity for a sample relative to a comparable control, e.g., the value observed from the derivatived lacZ construct, where the construct has a corresponding sense codon at desired position rather than a selector codon. In the tRNA molecule, Thymine (T) is replaced with Uracil (U). In addition, additional modifications to the bases can be present. The invention also includes conservative variations of O-tRNA. For example, conservative variations of O-tRNA include those molecules that function like the O-tRNA and maintain the tRNA L-shaped structure, but do not have the same sequence (and are other than wild type tRNA molecules). See also the section herein entitled �Nucleic Acid and Polypeptide Sequence and Variants.� The composition comprising an O-tRNA can further include an orthogonal aminoacyl-tRNA synthetase (O-RS), where the O-RS preferentially aminoacylates the O-tRNA with a selected amino acid (e.g., an unnatural amino acid). In certain embodiments, a composition including an O-tRNA can further include a translation system (e.g., an in vitro or an in vivo translation system). A nucleic acid comprising a polynucleotide encoding a polypeptide of interest, wherein the polynucleotide comprises one or more selector codons recognized by the O-tRNA, or a combination of one or more of these, can also be present in the cell or other translation system. See also, the section herein entitled �Orthogonal Aminoacyl-tRNA Synthetases (O-RS).� Methods of producing an orthogonal tRNA (O-tRNA), e.g., an O-tRNA, are also a feature of the present invention. A tRNA, e.g., an O-tRNA, produced by the method is also a feature of the present invention. Methods of producing an orthogonal tRNA include mutating the anticodon loop of each of a pool of tRNA's to allow recognition of a selector codon (e.g., an amber codon, an opal codon, a four base codon, etc.), thereby providing a plurality of potential O-tRNA's; and analyzing secondary structure of a member of the plurality potential O-tRNA to identify non-canonical base pairs in the secondary structure, and optionally mutating the non-canonical base pairs (e.g., the non-canonical base pairs are mutated to canonical base pairs). The non-canonical base pairs can be located in the stem region of the secondary structure. An O-tRNA may possess an improvement of one or more characteristics or activities, such as improvement in orthogonality for a desired organism compared to the starting material, e.g., the plurality of tRNA sequences, while preserving its affinity towards a desired RS. Alternatively, O-tRNA's may be developed by mutating a known tRNA to modulate its interaction with or binding affinity to one or more molecules that influence translation or are components of translation machinery. Such components include, but are not limited to, elongation factors. Bacterial elongation factor EF-Tu plays a key role in the elongation step in protein synthesis. Following aminoacylation of the tRNA by tRNA synthetase, EF-Tu binds the aminoacylated tRNA and brings it to the A site of the ribosome. The ester bond between the charged amino acid and the tRNA is protected from spontaneous hydrolysis due to the binding between EF-Tu and aminoacylated tRNA. Stortchevoi et al. investigated mutants of the E. coli initiation tRNAfMet U50:G64 wobble base pair in the TψC stem, since this base pair was found to be a secondary negative determinant blocking the tRNA's activity in elongation, presumably due to a weakened interaction between the EF-Tu.GTP and aminoacylated tRNA (JBC 2003 278(20):17672-17679). Also, LaRiviere et al. described in Science 2001 Oct. 5; 294(5540):165-8 the thermodynamic contributions of the amino acid and the tRNA body to the overall binding affinity to EF-Tu. They indicated that the contributions of the tRNA body and the amino acid are independent of each other and that they compensate for one another when the tRNAs are correctly acylated. Alterations to the interaction between EF-Tu.GTP and the tRNA aminoacylated with the unnatural amino acid may affect the efficiency of the loading of the tRNA to the A site of the ribosome. Potential mutation sites may also be found by analyzing crystal structures of complexes between tRNA and other components of translational machinery such as EF-Tu. For example, Nissen et al. have indicated that EF-Tu.GTP binds directly to the phosphate backbone of the TψC stem of yeast phenylalanyl-transfer RNA (Phe-tRNA) (Science 1995 270(5241):1464-1472). The methods optionally include analyzing the homology of sequences of tRNA's and/or aminoacyl-tRNA synthetases to determine potential candidates for an O-tRNA, O-RS and/or pairs thereof, that appear to be orthogonal for a specific organism. Computer programs known in the art and described herein can be used for the analysis. In one example, to choose potential orthogonal translational components for use in a prokaryotic organism, a synthetase and/or a tRNA is chosen that does not display unusual homology to prokaryotic organisms. A pool of tRNA's can also be produced by a consensus strategy. For example, the pool of tRNA's is produced by aligning a plurality of tRNA sequences; determining a consensus sequence; and generating a library of tRNA's using at least a portion, most of, or the entire consensus sequence. For example, a consensus sequence can be compiled with a computer program, e.g., the GCG program pileup. Optionally, degenerate positions determined by the program are changed to the most frequent base at those positions. A library is synthesized by techniques known in the art using the consensus sequence. For example, overlap extension of oligonucleotides in which each site of the tRNA gene can be synthesized as a doped mixture of 90% the consensus sequence and 10% a mixture of the other 3 bases can be used to provide the library based on the consensus sequence. Other mixtures can also be used, e.g., 75% the consensus sequence and 25% a mixture of the other 3 bases, 80% the consensus sequence and 20% a mixture of the other 3 bases, 95% the consensus sequence and 5% a mixture of the other 3 bases, etc. Libraries of mutant tRNA's can be generated using various mutagenesis techniques known in the art. For example, the mutant tRNA's can be generated by site-specific mutations, random point mutations, homologous recombination, DNA shuffling or other recursive mutagenesis methods, chimeric construction or any combination thereof. Additional mutations can be introduced at a specific position(s), e.g., at a non-conservative position(s), or at a conservative position(s), at a randomized position(s), or a combination thereof in a desired loop or region of a tRNA, e.g., an anticodon loop, the acceptor stem, D arm or loop, variable loop, TψC arm or loop, other regions of the tRNA molecule, or a combination thereof. Mutations may include matched base pairs in the stem region. Typically, an O-tRNA is obtained by subjecting to negative selection a population of cells of a first species, where the cells comprise a member of the plurality of potential O-tRNA's. The negative selection eliminates cells that comprise a member of the plurality of potential O-tRNA's that is aminoacylated by an aminoacyl-tRNA synthetase (RS) that is endogenous to the cells. This provides a pool of tRNA's that are orthogonal to the cell of the first species. In certain embodiments of the negative selection, a selector codon(s) is introduced into polynucleotide that encodes a negative selection marker, e.g., an enzyme that confers antibiotic resistance, e.g., β-lactamase, an enzyme that confers a detectable product, e.g., β-galactosidase, chloramphenicol acetyltransferase (CAT), e.g., a toxic product, such as barnase, at a non-essential position, etc. Screening/selection can be done by growing the population of cells in the presence of a selection agent (e.g., an antibiotic, such as ampicillin). In one embodiment, the concentration of the selection agent is varied. For example, to measure the activity of suppressor tRNA's, a selection system is used that is based on the in vivo suppression of selector codon, e.g., nonsense or frameshift mutations introduced into a polynucleotide that encodes a negative selection marker, e.g., a gene for β-lactamase (bla). For example, polynucleotide variants, e.g., bla variants, with, e.g., TAG, AGGA, and TGA, at position a certain position, are constructed. Cells, e.g., bacteria, are transformed with these polynucleotides. In the case of an orthogonal tRNA, which cannot be efficiently charged by endogenous E. coli synthetases, antibiotic resistance, e.g., ampicillin resistance, should be about or less than that for a bacteria transformed with no plasmid. If the tRNA is not orthogonal, or if a heterologous synthetase capable of charging the tRNA is co-expressed in the system, a higher level of antibiotic, e.g., ampicillin, resistance is be observed. Cells, e.g., bacteria, are chosen that are unable to grow on LB agar plates with antibiotic concentrations about equal to cells transformed with no plasmids. In the case of a toxic product (e.g., ribonuclease barnase), when a member of the plurality of potential tRNA's is aminoacylated by endogenous host, e.g., Escherichia coli synthetases (i.e., it is not orthogonal to the host, e.g., Escherichia coli synthetases), the selector codon is suppressed and the toxic polynucleotide product produced leads to cell death. Cells harboring orthogonal tRNA or non-functional tRNA's survive. In one embodiment, the pool of tRNA's that are orthogonal to a desired organism are then subjected to a positive selection in which a selector codon is placed in a positive selection marker, e.g., encoded by a drug resistance gene, such a β-lactamase gene. The positive selection is performed on cell comprising a polynucleotide encoding or comprising a member of the pool of tRNA's, a polynucleotide encoding a positive selection marker, and a polynucleotide encoding cognate RS. These polynucleotides are expressed in the cell and the cell is grown in the presence of a selection agent, e.g., ampicillin. tRNA's are then selected for their ability to be aminoacylated by the coexpressed cognate synthetase and to insert an amino acid in response to this selector codon. Typically, these cells show an enhancement in suppression efficiency compared to cells harboring non-functional tRNA's, or tRNA's that cannot efficiently be recognized by the synthetase of interest. The cell harboring the non-functional or tRNA's that are not efficiently recognized by the synthetase of interest are sensitive to the antibiotic. Therefore, tRNA's that: (i) are not substrates for endogenous host, e.g., Escherichia coli, synthetases; (ii) can be aminoacylated by the synthetase of interest; and (iii) are functional in translation survive both selections. The stringency of the selection, e.g., the positive selection, the negative selection or both the positive and negative selection, in the above described-methods, optionally may be varied. For example, because barnase is an extremely toxic protein, the stringency of the negative selection can be controlled by introducing different numbers of selector codons into the barnase gene and/or by using an inducible promoter. In another example, the concentration of the selection or screening agent is varied (e.g., ampicillin). In one aspect, the stringency is varied because the desired activity can be low during early rounds. Thus, less stringent selection criteria are applied in early rounds and more stringent criteria are applied in later rounds of selection. In certain embodiments, the negative selection, the positive selection, or both the negative and positive selection can be repeated multiple times. Multiple different negative selection markers, positive selection markers or both negative and positive selection markers can be used. In certain embodiments, the positive and negative selection marker can be the same. Other types of selections/screening can be used in the invention for producing orthogonal translational components, e.g., an O-tRNA, an O-RS, and an O-tRNA/O-RS pair. For example, the negative selection marker, the positive selection marker or both the positive and negative selection markers can include a marker that fluoresces or catalyzes a luminescent reaction in the presence of a suitable reactant. In another embodiment, a product of the marker is detected by fluorescence-activated cell sorting (FACS) or by luminescence. Optionally, the marker includes an affinity based screening marker. See, Francisco, J. A., et al., (1993) Production and fluorescence-activated cell sorting of Escherichia coli expressing a functional antibody fragment on the external surface. Proc Natl Acad Sci U S A. 90:10444-8. Additional methods for producing a recombinant orthogonal tRNA can be found, e.g., in U.S. patent application Ser. Nos. 10/126,931, entitled �Methods and Compositions for the Production of Orthogonal tRNA-Aminoacyl tRNA Synthetase Pairs� and 10/126,127, entitled �In vivo Incorporation of Unnatural Amino Acids,� and U.S. Ser. No. 10/825,867 entitled �EXPANDING THE EUKARYOTIC GENETIC CODE.� See also, Forster et al., (2003) Programming peptidomimetic synthetases by translating genetic codes designed de novo. PNAS 100(11):6353-6357; and, Feng et al., (2003), Expanding tRNA recognition of a tRNA synthetase by a single amino acid change, PNAS 100(10): 5676-5681. A tRNA of the present invention may be aminoacylated with a desired amino acid by any method or technique, including but not limited to, chemical or enzymatic aminoacylation. Aminoacylation may be accomplished by aminoacyl tRNA synthetases or by other enzymatic molecules, including but not limited to, ribozymes. The term �ribozyme� is interchangeable with �catalytic RNA.� Cech and coworkers (Cech, 1987, Science, 236:1532-1539; McCorkle et al., 1987, Concepts Biochem. 64:221-226) demonstrated the presence of naturally occurring RNAs that can act as catalysts (ribozymes). However, although these natural RNA catalysts have only been shown to act on ribonucleic acid substrates for cleavage and splicing, the recent development of artificial evolution of ribozymes has expanded the repertoire of catalysis to various chemical reactions. Studies have identified RNA molecules that can catalyze aminoacyl-RNA bonds on their own (2′)3′-termini (Illangakekare et al., 1995 Science 267:643-647), and an RNA molecule which can transfer an amino acid from one RNA molecule to another (Lohse et al., 1996, Nature 381:442-444). U.S. Patent Application Publication 2003/0228593, which is incorporated by reference herein, describes methods to construct ribozymes and their use in aminoacylation of tRNAs with naturally encoded and non-naturally encoded amino acids. Substrate-immobilized forms of enzymatic molecules that can aminoacylate tRNAs, including but not limited to, ribozymes, may enable efficient affinity purification of the aminoacylated products. Examples of suitable substrates include agarose, sepharose, and magnetic beads. The production and use of a substrate-immobilized form of ribozyme for aminoacylation is described in Chemistry and Biology 2003, 10:1077-1084 and U.S. Patent Application Publication 2003/0228593, which is incorporated by reference herein. Chemical aminoacylation methods include, but are not limited to, those introduced by Hecht and coworkers (Hecht, S. M. Acc. Chem. Res. 1992, 25, 545; Heckler, T. G.; Roesser, J. R.; Xu, C.; Chang, P.; Hecht, S. M. Biochemistry 1988, 27, 7254; Hecht, S. M.; Alford, B. L.; Kuroda, Y.; Kitano, S. J. Biol. Chem. 1978, 253, 4517) and by Schultz, Chamberlin, Dougherty and others (Cornish, V. W.; Mendel, D.; Schultz, P. G. Angew. Chem. Int. Ed. Engl. 1995, 34, 621; Robertson, S. A.; Ellman, J. A.; Schultz, P. G. J. Am. Chem. Soc. 1991, 113, 2722; Noren, C. J.; Anthony-Cahill, S. J.; Griffith, M. C.; Schultz, P. G. Science 1989, 244, 182; Bain, J. D.; Glabe, C. G.; Dix, T. A.; Chamberlin, A. R. J. Am. Chem. Soc. 1989, 111, 8013; Bain, J. D. et al. Nature 1992, 356, 537; Gallivan, J. P.; Lester, H. A.; Dougherty, D. A. Chem. Biol. 1997, 4, 740; Turcatti, et al. J. Biol. Chem. 1996, 271, 19991; Nowak, M. W. et al. Science, 1995, 268, 439; Saks, M. E. et al. J. Biol. Chem. 1996, 271, 23169; Hohsaka, T. et al. J. Am. Chem. Soc. 1999, 121, 34), to avoid the use of synthetases in aminoacylation. Such methods or other chemical aminoacylation methods may be used to aminoacylate tRNA molecules of the invention. Biosynthetic methods that employ chemically modified aminoacyl-tRNAs have been used to incorporate several biophysical probes into proteins synthesized in vitro. See the following publications and references cited within: Brunner, J. New Photolabeling and crosslinking methods, Annu. Rev Biochem, 62:483-514 (1993); and, Krieg, U. C., Walter, P., Hohnson, A. E. Photocrosslinking of the signal sequence of nascent preprolactin of the 54-kilodalton polypeptide of the signal recognition particle, Proc. Natl. Acad. Sci, 83(22):8604-8608 (1986). Previously, it has been shown that unnatural amino acids can be site-specifically incorporated into proteins in vitro by the addition of chemically aminoacylated suppressor tRNAs to protein synthesis reactions programmed with a gene containing a desired amber nonsense mutation. Using these approaches, one can substitute a number of the common twenty amino acids with close structural homologues, e.g., fluorophenylalanine for phenylalanine, using strains auxotropic for a particular amino acid. See, e.g., Noren, C. J., Anthony-Cahill, Griffith, M. C., Schultz, P. G. A general method for site-specific incorporation of unnatural amino acids into proteins, Science, 244:182-188 (1989); M. W. Nowak, et al., Science 268:439-42 (1995); Bain, J. D., Glabe, C. G., Dix, T. A., Chamberlin, A. R., Diala, E. S. Biosynthetic site-specific Incorporation of a non-natural amino acid into a polypeptide, J. Am. Chem Soc, 111:8013-8014 (1989); N. Budisa et al., FASEB J. 13:41-51 (1999); Ellman, J. A., Mendel, D., Anthony-Cahill, S., Noren, C. J., Schultz, P. G. Biosynthetic method for introducing unnatural amino acids site-specifically into proteins, Methods in Enz., vol. 202, 301-336 (1992); and, Mendel, D., Cornish, V. W. & Schultz, P. G. Site-Directed Mutagenesis with an Expanded Genetic Code, Annu Rev Biophys. Biomol Struct. 24, 435-62 (1995). For example, a suppressor tRNA was prepared that recognized the stop codon UAG and was chemically aminoacylated with an unnatural amino acid. Conventional site-directed mutagenesis was used to introduce the stop codon TAG, at the site of interest in the protein gene. See, e.g., Sayers, J. R., Schmidt, W. Eckstein, F. 5′-3′ Exonucleases in phosphorothioate-based olignoucleotide-directed mutagensis, Nucleic Acids Res, 16(3):791-802 (1988). When the acylated suppressor tRNA and the mutant gene were combined in an in vitro transcription/translation system, the unnatural amino acid was incorporated in response to the UAG codon which gave a protein containing that amino acid at the specified position. Experiments using [3H]-Phe and experiments with α-hydroxy acids demonstrated that only the desired amino acid is incorporated at the position specified by the UAG codon and that this amino acid is not incorporated at any other site in the protein. See, e.g., Noren, et al, supra; Kobayashi et al., (2003) Nature Structural Biology 10(6):425-432; and, Ellman, J. A., Mendel, D., Schultz, P. G. Site-specific incorporation of novel backbone structures into proteins, Science, 255(5041):197-200 (1992). Methods for generating catalytic RNA may involve generating separate pools of randomized ribozyme sequences, performing directed evolution on the pools, screening the pools for desirable aminoacylation activity, and selecting sequences of those ribozymes exhibiting desired aminoacylation activity. Ribozymes can comprise motifs and/or regions that facilitate acylation activity, such as a GGU motif and a U-rich region. For example, it has been reported that U-rich regions can facilitate recognition of an amino acid substrate, and a GGU-motif can form base pairs with the 3′ termini of a tRNA. In combination, the GGU and motif and U-rich region facilitate simultaneous recognition of both the amino acid and tRNA simultaneously, and thereby facilitate aminoacylation of the 3′ terminus of the tRNA. Ribozymes can be generated by in vitro selection using a partially randomized r24mini conjugated with tRNAAsn CCCG, followed by systematic engineering of a consensus sequence found in the active clones. An exemplary ribozyme obtained by this method is termed �Fx3 ribozyme� and is described in U.S. Pub. App. No. 2003/0228593, the contents of which is incorporated by reference herein, acts as a versatile catalyst for the synthesis of various aminoacyl-tRNAs charged with cognate non-natural amino acids. Immobilization on a substrate may be used to enable efficient affinity purification of the aminoacylated tRNAs. Examples of suitable substrates include, but are not limited to, agarose, sepharose, and magnetic beads. Ribozymes can be immobilized on resins by taking advantage of the chemical structure of RNA, such as the 3′-cis-diol on the ribose of RNA can be oxidized with periodate to yield the corresponding dialdehyde to facilitate immobilization of the RNA on the resin. Various types of resins can be used including inexpensive hydrazide resins wherein reductive amination makes the interaction between the resin and the ribozyme an irreversible linkage. Synthesis of aminoacyl-tRNAs can be significantly facilitated by this on-column aminoacylation technique. Kourouklis et al. Methods 2005; 36:239-4 describe a column-based aminoacylation system. Isolation of the aminoacylated tRNAs can be accomplished in a variety of ways. One suitable method is to elute the aminoacylated tRNAs from a column with a buffer such as a sodium acetate solution with 10 mM EDTA, a buffer containing 50 mM N-(2-hydroxyethyl)piperazine-N′-(3-propanesulfonic acid), 12.5 mM KCl, pH 7.0, 10 mM EDTA, or simply an EDTA buffered water (pH 7.0). The aminoacylated tRNAs of the present invention can be added to translation reactions in order to incorporate the amino acid with which the tRNA was aminoacylated in a position of choice in a polypeptide made by the translation reaction. Examples of translation systems in which the aminoacylated tRNAs of the present invention may be used include, but are not limited to cell lysates. Cell lysates provide reaction components necessary for in vitro translation of a polypeptide from an input mRNA. Examples of such reaction components include but are not limited to ribosomal proteins, rRNA, amino acids, tRNAs, GTP, ATP, translation initiation and elongation factors and additional factors associated with translation. Additionally, translation systems may be batch translations or compartmentalized translation. Batch translation systems combine reaction components in a single compartment while compartmentalized translation systems separate the translation reaction components from reaction products that can inhibit the translation efficiency. Such translation systems are available commercially. Further, a coupled transcription/translation system may be used. Coupled transcription/translation systems allow for both transcription of an input DNA into a corresponding mRNA, which is in turn translated by the reaction components. An example of a commercially available coupled transcription/translation is the Rapid Translation System (RTS, Roche Inc.). The system includes a mixture containing E. coli lysate for providing translational components such as ribosomes and translation factors. Additionally, an RNA polymerase is included for the transcription of the input DNA into an mRNA template for use in translation. RTS can use compartmentalization of the reaction components by way of a membrane interposed between reaction compartments, including a supply/waste compartment and a transcription/translation compartment. Aminoacylation of tRNA may be performed by other agents, including but not limited to, transferases, polymerases, catalytic antibodies, multi-functional proteins, and the like. Orthogonal Aminoacyl-tRNA Synthetases (O-RS) An O-RS preferentially aminoacylates an O-tRNA of the present invention with a selected amino acid in vitro or in vivo. An O-RS of the present invention can be provided to the translation system (e.g., in vitro translation components, or a cell) by a polypeptide that includes an O-RS and/or by a polynucleotide that encodes an O-RS or a portion thereof. An O-RS, or a portion thereof, is encoded by a polynucleotide sequence or a complementary polynucleotide sequence thereof, or a conservative variation thereof. An O-tRNA of the present invention may be aminoacylated by a number of different O-RS molecules, including but not limited to, those disclosed herein. Methods for identifying an orthogonal aminoacyl-tRNA synthetase (O-RS), e.g., an O-RS, for use with an O-tRNA, e.g., an O-tRNA, are also a feature of the present invention. For example a method includes subjecting to positive selection a population of cells of a first species, where the cells each comprise: 1) a member of a plurality of aminoacyl-tRNA synthetases (RSs), where the plurality of RSs comprise mutant RSs, RSs derived from a species other than the first species or both mutant RSs and RSs derived from a species other than the first species; 2) the orthogonal tRNA (O-tRNA) from a second species; and 3) a polynucleotide that encodes a positive selection marker and comprises at least one selector codon. Cells are selected or screened for those that show an enhancement in suppression efficiency compared to cells lacking or with a reduced amount of the member of the plurality of RSs. Cells having an enhancement in suppression efficiency comprise an active RS that aminoacylates the O-tRNA. A level of aminoacylation (in vitro or in vivo) by the active RS of a first set of tRNA's from the first species is compared to the level of aminoacylation (in vitro or in vivo) by the active RS of a second set of tRNA's from the second species. The level of aminoacylation can be determined by a detectable substance (e.g., a labeled amino acid or unnatural amino acid). The active RS that more efficiently aminoacylates the second set of tRNA's compared to the first set of tRNA's is selected, thereby providing the orthogonal aminoacyl-tRNA synthetase for use with the O-tRNA. An O-RS, e.g., an O-RS, identified by the method is also a feature of the present invention. Any of a number of assays can be used to determine aminoacylation. These assays can be performed in vitro or in vivo. For example, in vitro aminoacylation assays are described in, e.g., Hoben, P., and Soll, D. (1985) Methods Enzymol. 113:55-59 and in U.S. Patent Application Publication No. 2003/0228593. Aminoacylation can also be determined by using a reporter along with orthogonal translation components and detecting the reporter in a cell expressing a polynucleotide comprising at least one selector codon that encodes a protein. See also, U.S. patent application Ser. No. 10/126,927, entitled �IN VIVO INCORPORATION OF UNNATURAL AMINO ACIDS;� and, U.S. Ser. No. 10/825,867 entitled �EXPANDING THE EUKARYOTIC GENETIC CODE.� An identified O-RS can be further manipulated to alter the substrate specificity of the synthetase so that only a desired unnatural amino acid, but not any of the common 20 amino acids, are charged to the O-tRNA. Methods to generate an orthogonal aminoacyl tRNA synthetases with a substrate specificity for an unnatural amino acid include mutating the synthetase, e.g., at the active site in the synthetase, at the editing mechanism site in the synthetase, at different sites by combining different domains of synthetases, or the like, and applying a selection process. A strategy is used that is based on the combination of a positive selection followed by a negative selection. In the positive selection, suppression of the selector codon introduced at a non-essential position(s) of a positive marker allows cells to survive under positive selection pressure. In the presence of both natural and unnatural amino acids, survivors thus encode active synthetases charging the orthogonal suppressor tRNA with either a natural or unnatural amino acid. In the negative selection, suppression of a selector codon introduced at a non-essential position(s) of a negative marker removes synthetases with natural amino acid specificities. Survivors of the negative and positive selection encode synthetases that aminoacylate (charge) the orthogonal suppressor tRNA with unnatural amino acids only. These synthetases can then be subjected to further mutagenesis, e.g., DNA shuffling or other recursive mutagenesis methods. The library of mutant O-RSs can be generated using various mutagenesis techniques known in the art. For example, the mutant RSs can be generated by site-specific mutations, random point mutations, homologous recombination, DNA shuffling or other recursive mutagenesis methods, chimeric construction or any combination thereof. For example, a library of mutant RSs can be produced from two or more other, e.g., smaller, less diverse �sub-libraries.� Chimeric libraries of RSs are also included in the invention. It should be noted that libraries of tRNA synthetases from various organisms (e.g., microorganisms such as eubacteria or archaebacteria) such as libraries that comprise natural diversity (see, e.g., U.S. Pat. No. 6,238,884 to Short et al; U.S. Pat. No. 5,756,316 to Schallenberger et al; U.S. Pat. No. 5,783,431 to Petersen et al; U.S. Pat. No. 5,824,485 to Thompson et al; U.S. Pat. No. 5,958,672 to Short et al), are optionally constructed and screened for orthogonal pairs. Once the synthetases are subject to the positive and negative selection/screening strategy, these synthetases can then be subjected to further mutagenesis. For example, a nucleic acid that encodes the O-RS can be isolated; a set of polynucleotides that encode mutated O-RSs (e.g., by random mutagenesis, site-specific mutagenesis, recombination or any combination thereof) can be generated from the nucleic acid; and, these individual steps or a combination of these steps can be repeated until a mutated O-RS is obtained that preferentially aminoacylates the O-tRNA with the unnatural amino acid. In one aspect of the present invention, the steps are performed multiple times, e.g., at least two times. Additional levels of selection/screening stringency can also be used in the methods of the present invention, for producing O-tRNA, O-RS, or pairs thereof. The selection or screening stringency can be varied on one or both steps of the method to produce an O-RS. This could include, e.g., varying the amount of selection/screening agent that is used, etc. Additional rounds of positive and/or negative selections can also be performed. Selecting or screening can also comprise one or more positive or negative selection or screening that includes, e.g., a change in amino acid permeability, a change in translation efficiency, a change in translational fidelity, etc. Typically, the one or more change is based upon a mutation in one or more gene in an organism in which an orthogonal tRNA-tRNA synthetase pair is used to produce protein. Other types of selections can be used in the present invention for, e.g., O-RS, O-tRNA, and O-tRNA/O-RS pair. The positive selection marker can be any of a variety of molecules including, but not limited to, a product that provides a nutritional supplement for growth and the selection is performed on a medium that lacks the nutritional supplement. Examples of polynucleotides that encode positive selection markers include, but are not limited to, e.g., a reporter gene based on complementing the amino acid auxotrophy of a cell, a his3 gene (e.g., where the his3 gene encodes an imidazole glycerol phosphate dehydratase, detected by providing 3-aminotriazole (3-AT)), ura3 gene, leu2 gene, lys2 gene, lacZ gene, adh gene, etc. See, e.g., G. M. Kishore, & D. M. Shah, (1988), Amino acid biosynthesis inhibitors as herbicides, Annual Review of Biochemistry 57:627-663. In one embodiment, lacZ production is detected by ortho-nitrophenyl-β-D-galactopyranoside (ONPG) hydrolysis. See, e.g., I. G. Serebriiskii, & E. A. Golemis, (2000), Uses of lacZ to study gene function: evaluation of beta-galactosidase assays employed in the yeast two-hybrid system, Analytical Biochemistry 285:1-15. Additional positive selection markers include, e.g., luciferase, green fluorescent protein (GFP), YFP, EGFP, RFP, the product of an antibiotic resistant gene (e.g., chloramphenicol acetyltransferase (CAT)), a transcriptional modulator protein (e.g., GAL4), etc. Optionally, a polynucleotide that encodes a positive selection marker comprises a selector codon. A polynucleotide that encodes the positive selection marker can be operably linked to a response element. An additional polynucleotide that encodes a transcriptional modulator protein that modulates transcription from the response element, and comprises at least one selector codon, can also be present. The incorporation of the unnatural amino acid into the transcriptional modulator protein by the O-tRNA aminoacylated with the unnatural amino acid results in transcription of the polynucleotide (e.g., reporter gene) encoding the positive selection marker. Optionally, the selector codon is located in or substantially near a portion of the polynucleotide that encodes a DNA binding domain of the transcriptional modulator protein. A polynucleotide that encodes the negative selection marker can also be operably linked to a response element from which transcription is mediated by the transcriptional modulator protein. See, e.g., A. J. DeMaggio, et al., (2000), The yeast split-hybrid system, Method Enzymol. 328:128-137; H. M. Shih, et al., (1996), A positive genetic selection for disrupting protein-protein interactions: identification of CREB mutations that prevent association with the coactivator CBP, Proc. Natl. Acad. Sci. U.S.A. 93:13896-13901; M. Vidal, et al., (1996), Genetic characterization of a mammalian protein-protein interaction domain by using a yeast reverse two-hybrid system, Proc. Natl. Acad. Sci. U.S.A. 93:10321-10326; and, M. Vidal, et al., (1996), Reverse two-hybrid and one-hybrid systems to detect dissociation of protein-protein and DNA-protein interactions (Proc. Natl. Acad. Sci. U.S.A. 93:10315-10320). The incorporation of a natural amino acid into the transcriptional modulator protein by the O-tRNA aminoacylated with a natural amino acid results in transcription of the negative selection marker. Optionally, the negative selection marker comprises a selector codon. The positive selection marker and/or negative selection marker of the invention can comprise at least two selector codons, which each or both can comprise at least two different selector codons or at least two of the same selector codons. The transcriptional modulator protein is a molecule that binds (directly or indirectly) to a nucleic acid sequence (e.g., a response element) and modulates transcription of a sequence that is operably linked to the response element. A transcriptional modulator protein can be a transcriptional activator protein (e.g., GAL4, nuclear hormone receptors, API, CREB, LEF/tcf family members, SMADs, VP16, SP1, etc.), a transcriptional repressor protein (e.g., nuclear hormone receptors, Groucho/tle family, Engrailed family, etc), or a protein that can have both activities depending on the environment (e.g., LEF/tcf, homobox proteins, etc.). A response element is typically a nucleic acid sequence that is recognized by the transcriptional modulator protein or an additional agent that acts in concert with the transcriptional modulator protein. Another example of a transcriptional modulator protein is the transcriptional activator protein, GAL4. See, e.g., A. Laughon, et al., (1984), Identification of two proteins encoded by the Saccharomyces cerevisiae GAL4 gene, Molecular & Cellular Biology 4:268-275; A. Laughon, & R. F. Gesteland, (1984), Primary structure of the Saccharomyces cerevisiae GAL4 gene, Molecular & Cellular Biology 4:260-267; L. Keegan, et al., (1986), Separation of DNA binding from the transcription-activating function of a eukaryotic regulatory protein, Science 231:699-704; and, M. Ptashne, (1988), How eukaryotic transcriptional activators work, Nature 335:683-689. The N-terminal 147 amino acids of this 881 amino acid protein form a DNA binding domain (DBD) that binds DNA sequence specifically. See, e.g., M. Carey, et al., (1989), An amino-terminal fragment of GAL4 binds DNA as a dimer, J. Mol. Biol. 209:423-432; and, E. Giniger, et al., (1985), Specific DNA binding of GAL4, a positive regulatory protein of yeast, Cell 40:767-774. The DBD is linked, by an intervening protein sequence, to a C-terminal 113 amino acid activation domain (AD) that can activate transcription when bound to DNA. See, e.g., J. Ma, & M. Ptashne, (1987), Deletion analysis of GAL4 defines two transcriptional activating segments, Cell 48:847-853: and, J. Ma, & M. Ptashne, (1987), The carboxy-terminal 30 amino acids of GAL4 are recognized by GAL80, Cell 50:137-142. By placing amber codons towards, e.g., the N-terminal DBD of a single polypeptide that contains both the N-terminal DBD of GAL4 and its C-terminal AD, amber suppression by the O-tRNA/O-RS pair can be linked to transcriptional activation by GAL4. GAL4 activated reporter genes can be used to perform both positive and negative selections with the gene. The medium used for negative selection can comprise a selecting or screening agent that is converted to a detectable substance by the negative selection marker. In one aspect of the invention, the detectable substance is a toxic substance. A polynucleotide that encodes a negative selection marker can be, e.g., an ura3 gene. For example, the URA3 reporter can be placed under control of a promoter that contains GAL4 DNA binding sites. When the negative selection marker is produced, e.g., by translation of a polynucleotide encoding the GAL4 with selector codons, GAL4 activates transcription of URA3. The negative selection is accomplished on a medium that comprises 5-flubroorotic acid (5-FOA), which is converted into a detectable substance (e.g., a toxic substance which kills the cell) by the gene product of the ura3 gene. See, e.g., J. D. Boeke, et al., (1984), A positive selection for mutants lacking orotidine-5′-phosphate decarboxylase activity in yeast: 5-fluoroorotic acid resistance, Molecular & General Genetics 197:345-346); M. Vidal, et al., (1996), Genetic characterization of a mammalian protein-protein interaction domain by using a yeast reverse two-hybrid system., Proc. Natl. Acad. Sci. U.S.A. 93:10321-10326; and, M. Vidal, et al., (1996), Reverse two-hybrid and one-hybrid systems to detect dissociation of protein-protein and DNA-protein interactions., Proc. Natl. Acad. Sci. U.S.A. 93:10315-10320. As with the positive selection marker, the negative selection marker can also be any of a variety of molecules. The positive selection marker and/or the negative selection marker may be a polypeptide that fluoresces or catalyzes a luminescent reaction in the presence of a suitable reactant. For example, negative selection markers include, but are not limited to, e.g., luciferase, green fluorescent protein (GFP), YFP, EGFP, RFP, the product of an antibiotic resistant gene (e.g., chloramphenicol acetyltransferase (CAT)), the product of a lacZ gene, transcriptional modulator protein, etc. The positive selection marker and/or the negative selection marker may be detected by fluorescence-activated cell sorting (FACS) or by luminescence. The positive selection marker and/or negative selection marker may comprise an affinity based screening marker. The same polynucleotide can encode both the positive selection marker and the negative selection marker. For example, the positive selection step, the negative selection step or both the positive and negative selection steps and can include using a reporter, wherein the reporter is detected by fluorescence-activated cell sorting (FACS). For example, a positive selection can be done first with a positive selection marker, e.g., chloramphenicol acetyltransferase (CAT) gene, where the CAT gene comprises a selector codon, e.g., an amber stop codon, in the CAT gene, which followed by a negative selection screen, that is based on the inability to suppress a selector codon(s), e.g., two or more, at positions within a negative marker, e.g., T7 RNA polymerase gene. The positive selection marker and the negative selection marker can be found on the same vector, e.g., plasmid. Expression of the negative marker drives expression of the reporter, e.g., green fluorescent protein (GFP). The stringency of the selection and screen can be varied, e.g., the intensity of the light need to fluorescence the reporter can be varied. A positive selection can be done with a reporter as a positive selection marker, which is screened by FACS, followed by a negative selection screen, that is based on the inability to suppress a selector codon(s), e.g., two or more, at positions within a negative marker, e.g., barnase gene. Optionally, the reporter is displayed on a cell surface, e.g., on a phage display or the like. Cell-surface display, e.g., the OmpA-based cell-surface display system, relies on the expression of a particular epitope, e.g., a poliovirus C3 peptide fused to an outer membrane porin OmpA, on the surface of the Escherichia coli cell. The epitope is displayed on the cell surface only when a selector codon in the protein message is suppressed during translation. The displayed peptide then contains the amino acid recognized by one of the mutant aminoacyl-tRNA synthetases in the library, and the cell containing the corresponding synthetase gene can be isolated with antibodies raised against peptides containing specific unnatural amino acids. The OmpA-based cell-surface display system was developed and optimized by Georgiou et al. as an alternative to phage display. See, Francisco, J. A., Campbell, R., Iverson, B. L. & Georgoiu, G. Production and fluorescence-activated cell sorting of Escherichia coli expressing a functional antibody fragment on the external surface. Proc. Natl. Acad. Sci. USA 90:10444-8 (1993). Other embodiments of the present invention include carrying one or more of the selection steps in vitro. The selected component, e.g., synthetase and/or tRNA, can then be introduced into a cell for use in vivo incorporation of an unnatural amino acid. Additional details for producing O-RS, and altering the substrate specificity of the synthetase can be found in U.S. patent application Ser. No. 10/126,931 entitled �Methods and Compositions for the Production of Orthogonal tRNA-Aminoacyl tRNA Synthetase Pairs;� and, U.S. Ser. No. 10/825,867 entitled �EXPANDING THE EUKARYOTIC GENETIC CODE,� which are incorporated by reference herein. Additional details for producing O-RS can be found in Hamano-Takaku et al., (2000) A mutant Escherichia coli Tyrosyl-tRNA Synthetase Utilizes the Unnatural Amino Acid Azatyrosine More Efficiently than Tyrosine, Journal of Biological Chemistry, 275(51):40324-40328; Kiga et al. (2002), An engineered Escherichia coli tyrosyl-tRNA synthetase for site-specific incorporation of an unnatural amino acid into proteins in eukaryotic translation and its application in a wheat germ cell-free system, PNAS 99(15): 9715-9723; and, Francklyn et al., (2002), Aminoacyl-tRNA synthetases: Versatile players in the changing theater of translation; RNA, 8:1363-1372, each of which are incorporated by reference herein. Source and Host Organisms The translational components of the present invention are typically derived from non-eukaryotic organisms. For example, the orthogonal O-tRNA can be derived from a non-eukaryotic organism, e.g., an archaebacterium, such as Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Halobacterium such as Haloferax volcanii and Halobacterium species NRC-1, Archaeoglobus fulgidus, Pyrococcus furiosus, Pyrococcus horikoshii, Aeuropyrum pernix, or the like, or a eubacterium, such as Escherichia coli, Thermus thermophilus, Bacillus stearothermphilus, or the like, while the orthogonal O-RS can be derived from a non-eukaryotic organism, e.g., Methanobacterium thermoautotrophicum, Halobacterium such as Haloferax volcanii and Halobacterium species NRC-1, Archaeoglobus fulgidus, Pyrococcus furiosus, Pyrococcus horikoshii, Aeuropyrunm pernix, or the like, or a eubacterium, such as Escherichia coli, Thermus thermophilus, Bacillus stearothermiphilus, or the like. In one embodiment, eukaryotic sources can also be used, including but not limited to, plants, algae, protists, fungi, yeasts, animals (e.g., mammals, insects, arthropods, etc.), or the like. The individual components of an O-tRNA/O-RS pair can be derived from the same organism or different organisms. In one embodiment, the O-tRNA/O-RS pair is from the same organism. Alternatively, the O-tRNA and the O-RS of the O-tRNA/O-RS pair are from different organisms. For example, the O-tRNA can be derived from, e.g., a Halobacterium sp NRC-1, and the O-RS can be derived from, e.g., a Methanobacterium thermoautrophicum. The O-tRNA, O-RS or O-tRNA/O-RS pair can be selected or screened in vivo or in vitro and/or used in a cell, e.g., a non-eukaryotic cells (such as E. coli cell), or a eukaryotic cell, to produce a polypeptide with a selected amino acid (e.g., an unnatural amino acid). A non-eukaryotic cell can be from a variety of sources, such as the Archaea phylogenetic domain, including but not limited to, Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Halobacterium such as Haloferax volcanii and Halobacterium species NRC-1, Archaeoglobus fulgidus, Pyrococcus furiosus, Pyrococcus horikoshii, Aeuropyrum pernix, or the like, or can belong to the Eubacteria phylogenetic domain (including but not limited to, Escherichia coli, Thermus thermophilus, Bacillus stearothermophilus, Pseudomonas fluorescens, Pseudomonas aeruginosa, Pseudomonas putida, etc.), or the like. A eukaryotic cell can be from a variety of sources, including but not limited to, a plant (e.g., complex plant such as monocots, or dicots), an algae, a protist, a fungus, a yeast (including but not limited to, Saccharomyces cerevisiae), an animal (including but not limited to, a mammal, an insect, an arthropod, etc.), or the like. Compositions of cells with translational components of the present invention are also a feature of the present invention. See also U.S. Ser. No. 10/825,867 entitled �Expanding the Eukaryotic Genetic Code� for screening O-tRNA and/or O-RS in one species for use in another species. To express a polypeptide of interest with a selected amino acid in a host cell, one may subclone polynucleotides encoding a polypeptide of interest into an expression vector that contains a promoter to direct transcription, a transcription/translation terminator, and if for a nucleic acid encoding a protein, a ribosome binding site for translational initiation. Suitable bacterial promoters are well known in the art and described, e.g., in Sambrook et al. and Ausubel et al. Bacterial expression systems for expressing a polypeptide of interest are available in, including but not limited to, E. coli, Bacillus sp., Pseudomonas fluorescens, Pseudomonas aeruginosa, Pseudomonas putida, and Salmonella (Palva et al., Gene 22:229-235 (1983); Mosbach et al., Nature 302:543-545 (1983)). Kits for such expression systems are commercially available. Eukaryotic expression systems for mammalian cells, yeast, and insect cells are well known in the art and are also commercially available. A tRNA and/or RS of the present invention and/or a polypeptide of interest may be utilized and/or expressed in any number of suitable expression systems including, for example, yeast, insect cells, mammalian cells, and bacteria. A description of exemplary expression systems is provided below. Yeast As used herein, the term �yeast� includes any of the various yeasts capable of expressing a polypeptide of interest. Such yeasts include, but are not limited to, ascosporogenous yeasts (Endomycetales), basidiosporogenous yeasts and yeasts belonging to the Fungi imperfecti (Blastomycetes) group. The ascosporogenous yeasts are divided into two families, Spermophthoraceae and Saccharomycetaceae. The latter is comprised of four subfamilies, Schizosaccharomycoideae (e.g., genus Schizosaccharomyces), Nadsonioideae, Lipomycoideae and Saccharomycoideae (e.g., genera Pichia, Kluyveromyces and Saccharomyces). The basidiosporogenous yeasts include the genera Leucosporidium, Rhodosporidium, Sporidiobolus, Filobasidium, and Filobasidiella. Yeasts belonging to the Fungi Imperfecti (Blastomycetes) group are divided into two families, Sporobolomycetaceae (e.g., genera Sporobolomyces and Bullera) and Cryptococcaceae (e.g., genus Candida). Of particular interest for use with the present invention are species within the genera Pichia, Kluyveromyces, Saccharomyces, Schizosaccharomyces, Hansenula, Torulopsis, and Candida, including, but not limited to, P. pastoris, P. guillerimondii, S. cerevisiae, S. carlsbergensis, S. diastaticus, S. douglasii, S. kluyveri, S. norbensis, S. oviformis, K. lactis, K. fragilis, C. albicans, C. maltosa, and H. polymorpha. Yeast are generally available from a variety of sources including, but not limited to, the Yeast Genetic Stock Center, Department of Biophysics and Medical Physics, University of California (Berkeley, Calif.), and the American Type Culture Collection (�ATCC�) (Manassas, Va.). The term �yeast host� or �yeast host cell� includes yeast that can be, or has been, used as a recipient for recombinant vectors or other transfer DNA. The term includes the progeny of the original yeast host cell that has received the recombinant vectors or other transfer DNA. It is understood that the progeny of a single parental cell may not necessarily be completely identical in morphology or in genomic or total DNA complement to the original parent, due to accidental or deliberate mutation. Progeny of the parental cell that are sufficiently similar to the parent to be characterized by the relevant property, such as the presence of a nucleotide sequence encoding a polypeptide of interest, are included in the progeny intended by this definition. Expression and transformation vectors, including extrachromosomal replicons or integrating vectors, have been developed for transformation into many yeast hosts. For example, expression vectors have been developed for S. cerevisiae (Sikorski et al., GENETICS (1989) 122:19; Ito et al., J. BACTERIOL. (1983) 153:163; Hinnen et al., PROC. NATL. ACAD. SCI. USA (1978) 75:1929); C. albicans (Kurtz et al., MOL. CELL. BIOL. (1986) 6:142); C. maltosa (Kunze et al., J. BASIC MICROBIOL. (1985) 25:141); H. polymorpha (Gleeson et al., J. GEN. MICROBIOL. (1986) 132:3459; Roggenkamp et al., MOL. GENETICS AND GENOMICS (1986) 202:302); K. fragilis (Das et al., J. BACTERIOL. (1984) 158:1165); K. lactis (De Louvencourt et al., J. BACTERIOL. (1983) 154:737; Van den Berg et al., BIOTECHNOLOGY (NY) (1990) 8:135); P. guillerimondii (Kunze et al., J. BASIC MICROBIOL. (1985) 25:141); P. pastoris (U.S. Pat. Nos. 5,324,639; 4,929,555; and 4,837,148; Cregg et al., MOL. CELL. BIOL. (1985) 5:3376); Schizosaccharomyces pombe (Beach et al., NATURE (1982) 300:706); and Y. lipolytica; A. nidulans (Ballance et al., BIOCHEM. BIOPHYS. RES. COMMUN. (1983) 112:284-89; Tilburn et al., GENE (1983) 26:205-221; and Yelton et al., PROC. NATL. ACAD. SCI. USA (1984) 81:1470-74); A. niger (Kelly and Hynes, EMBO J. (1985) 4:475-479); T. reesia (EP 0 244 234); and filamentous fungi such as, e.g., Neurospora, Penicillium, Tolypocladium (WO 91/00357), each incorporated by reference herein. Control sequences for yeast vectors are known to those of ordinary skill in the art and include, but are not limited to, promoter regions from genes such as alcohol dehydrogenase (ADH) (EP 0 284 044); enolase; glucokinase; glucose-6-phosphate isomerase; glyceraldehyde-3-phosphate-dehydrogenase (GAP or GAPDH); hexokinase; phosphofructokinase; 3-phosphoglycerate mutase; and pyruvate kinase (PyK) (EP 0 329 203). The yeast PHO5 gene, encoding acid phosphatase, also may provide useful promoter sequences (Miyanohara et al., PROC. NATL. ACAD. SCI. USA (1983) 80:1). Other suitable promoter sequences for use with yeast hosts may include the promoters for 3-phosphoglycerate kinase (Hitzeman et al., J. BIOL. CHEM. (1980) 255:12073); and other glycolytic enzymes, such as pyruvate decarboxylase, triosephosphate isomerase, and phosphoglucose isomerase (Holland et al., BIOCHEMISTRY (1978) 17:4900; Hess et al., J. ADV. ENZYME REG. (1969) 7:149). Inducible yeast promoters having the additional advantage of transcription controlled by growth conditions may include the promoter regions for alcohol dehydrogenase 2; isocytochrome C; acid phosphatase; metallothionein; glyceraldehyde-3-phosphate dehydrogenase; degradative enzymes associated with nitrogen metabolism; and enzymes responsible for maltose and galactose utilization. Suitable vectors and promoters for use in yeast expression are further described in EP 0 073 657. Yeast enhancers also may be used with yeast promoters. In addition, synthetic promoters may also function as yeast promoters. For example, the upstream activating sequences (UAS) of a yeast promoter may be joined with the transcription activation region of another yeast promoter, creating a synthetic hybrid promoter. Examples of such hybrid promoters include the ADH regulatory sequence linked to the GAP transcription activation region. See U.S. Pat. Nos. 4,880,734 and 4,876,197, which are incorporated by reference herein. Other examples of hybrid promoters include promoters that consist of the regulatory sequences of the ADH2, GAL4, GAL10, or PHO5 genes, combined with the transcriptional activation region of a glycolytic enzyme gene such as GAP or PyK. See EP 0 164 556. Furthermore, a yeast promoter may include naturally occurring promoters of non-yeast origin that have the ability to bind yeast RNA polymerase and initiate transcription. Other control elements that may comprise part of the yeast expression vectors include terminators, for example, from GAPDH or the enolase genes (Holland et al., J. BIOL. CHEM. (1981) 256:1385). In addition, the origin of replication from the 2/plasmid origin is suitable for yeast. A suitable selection gene for use in yeast is the trp1 gene present in the yeast plasmid. See Tschumper et al., GENE (1980) 10:157; Kingsman et al., GENE (1979) 7:141. The trp1 gene provides a selection marker for a mutant strain of yeast lacking the ability to grow in tryptophan. Similarly, Leu2-deficient yeast strains (ATCC 20,622 or 38,626) are complemented by known plasmids bearing the Leu2 gene. Methods of introducing exogenous DNA into yeast hosts are known to those of ordinary skill in the art, and typically include, but are not limited to, either the transformation of spheroplasts or of intact yeast host cells treated with alkali cations. For example, transformation of yeast can be carried out according to the method described in Hsiao et al., PROC. NATL. ACAD. SCI. USA (1979) 76:3829 and Van Solingen et al., J. BACT. (1977) 130:946. However, other methods for introducing DNA into cells such as by nuclear injection, electroporation, or protoplast fusion may also be used as described generally in SAMBROOK ET AL., MOLECULAR CLONING: A LAB. MANUAL (2001). Yeast host cells may then be cultured using standard techniques known to those of ordinary skill in the art. Other methods for expressing heterologous proteins in yeast host cells are known to those of ordinary skill in the art. See generally U.S. Patent Publication No. 20020055169, U.S. Pat. Nos. 6,361,969; 6,312,923; 6,183,985; 6,083,723; 6,017,731; 5,674,706; 5,629,203; 5,602,034; and 5,089,398; U.S. Reexamined Patent Nos. RE37,343 and RE35,749; PCT Published Patent Applications WO 99/07862; WO 98/37208; and WO 98/26080; European Patent Applications EP 0 946 736; EP 0 732 403; EP 0 480 480; WO 90/10277; EP 0 340 986; EP 0 329 203; EP 0 324 274; and EP 0 164 556. See also Gellissen et al., ANTONIE VAN LEEUWENHOEK (1992) 62(1-2):79-93; Romanos et al., YEAST (1992) 8(6):423-488; Goeddel, METHODS IN ENZYMOLOGY (1990) 185:3-7, each incorporated by reference herein. The yeast host strains may be grown in fermentors during the amplification stage using standard feed batch fermentation methods known to those of ordinary skill in the art. The fermentation methods may be adapted to account for differences in a particular yeast host's carbon utilization pathway or mode of expression control. For example, fermentation of a Saccharomyces yeast host may require a single glucose feed, complex nitrogen source (e.g., casein hydrolysates), and multiple vitamin supplementation. In contrast, the methylotrophic yeast P. pastoris may require glycerol, methanol, and trace mineral feeds, but only simple ammonium (nitrogen) salts for optimal growth and expression. See, e.g., U.S. Pat. No. 5,324,639; Elliott et al., J. PROTEIN CHEM. (1990) 9:95; and Fieschko et al., BIOTECH. BIOENG. (1987) 29:1113, incorporated by reference herein. Such fermentation methods, however, may have certain common features independent of the yeast host strain employed. For example, a growth limiting nutrient, typically carbon, may be added to the fermentor during the amplification phase to allow maximal growth. In addition, fermentation methods generally employ a fermentation medium designed to contain adequate amounts of carbon, nitrogen, basal salts, phosphorus, and other minor nutrients (vitamins, trace minerals and salts, etc.). Examples of fermentation media suitable for use with Pichia are described in U.S. Pat. Nos. 5,324,639 and 5,231,178, which are incorporated by reference herein. Baculovirus-Infected Insect Cells The term �insect host� or �insect host cell� refers to a insect that can be, or has been, used as a recipient for recombinant vectors or other transfer DNA. The term includes the progeny of the original insect host cell that has been transfected. It is understood that the progeny of a single parental cell may not necessarily be completely identical in morphology or in genomic or total DNA complement to the original parent, due to accidental or deliberate mutation. Progeny of the parental cell that are sufficiently similar to the parent to be characterized by the relevant property, such as the presence of a nucleotide sequence encoding a polypeptide of interest, are included in the progeny intended by this definition. The selection of suitable insect cells for expression of a polypeptide of interest is known to those of ordinary skill in the art. Several insect species are well described in the art and are commercially available including Aedes aegypti, Bombyx mori, Drosophila melanogaster, Spodoptera frugiperda, and Trichoplusia ni. In selecting insect hosts for expression, suitable hosts may include those shown to have, inter alia, good secretion capacity, low proteolytic activity, and overall robustness. Insect are generally available from a variety of sources including, but not limited to, the Insect Genetic Stock Center, Department of Biophysics and Medical Physics, University of California (Berkeley, Calif.); and the American Type Culture Collection (�ATCC�) (Manassas, Va.). Generally, the components of a baculovirus-infected insect expression system include a transfer vector, usually a bacterial plasmid, which contains both a fragment of the baculovirus genome, and a convenient restriction site for insertion of the heterologous gene to be expressed; a wild type baculovirus with sequences homologous to the baculovirus-specific fragment in the transfer vector (this allows for the homologous recombination of the heterologous gene in to the baculovirus genome); and appropriate insect host cells and growth media. The materials, methods and techniques used in constructing vectors, transfecting cells, picking plaques, growing cells in culture, and the like are known in the art and manuals are available describing these techniques. After inserting the heterologous gene into the transfer vector, the vector and the wild type viral genome are transfected into an insect host cell where the vector and viral genome recombine. The packaged recombinant virus is expressed and recombinant plaques are identified and purified. Materials and methods for baculovirus/insect cell expression systems are commercially available in kit form from, for example, Invitrogen Corp. (Carlsbad, Calif.). These techniques are generally known to those of ordinary skill in the art and fully described in SUMMERS AND SMITH, TEXAS AGRICULTURAL EXPERIMENT STATION BULLETIN NO. 1555 (1987), herein incorporated by reference. See also, RICHARDSON, 39 METHODS IN MOLECULAR BIOLOGY: BACULOVIRUS EXPRESSION PROTOCOLS (1995); AUSUBEL ET AL., CURRENT PROTOCOLS IN MOLECULAR BIOLOGY 16.9-16.11 (1994); KING AND POSSEE, THE BACULOVIRUS SYSTEM: A LABORATORY GUIDE (1992); and O'REILLY ET AL., BACULOVIRUS EXPRESSION VECTORS: A LABORATORY MANUAL (1992). Indeed, the production of various heterologous proteins using baculovirus/insect cell expression systems is known to those of ordinary skill in the art. See, e.g., U.S. Pat. Nos. 6,368,825; 6,342,216; 6,338,846; 6,261,805; 6,245,528, 6,225,060; 6,183,987; 6,168,932; 6,126,944; 6,096,304; 6,013,433; 5,965,393; 5,939,285; 5,891,676; 5,871,986; 5,861,279; 5,858,368; 5,843,733; 5,762,939; 5,753,220; 5,605,827; 5,583,023; 5,571,709; 5,516,657; 5,290,686; WO 02/06305; WO 01/90390; WO 01/27301; WO 01/05956; WO 00/55345; WO 00/20032; WO 99/51721; WO 99/45130; WO 99/31257; WO 99/10515; WO 99/09193; WO 97/26332; WO 96/29400; WO 96/25496; WO 96/06161; WO 95/20672; WO 93/03173; WO 92/16619; WO 92/02628; WO 92/01801; WO 90/14428; WO 90/10078; WO 90/02566; WO 90/02186; WO 90/01556; WO 89/01038; WO 89/01037; WO 88/07082, which are incorporated by reference herein. Vectors that are useful in baculovirus/insect cell expression systems are known in the art and include, for example, insect expression and transfer vectors derived from the baculovirus Autographacalifornica nuclear polyhedrosis virus (AcNPV), which is a helper-independent, viral expression vector. Viral expression vectors derived from this system usually use the strong viral polyhedrin gene promoter to drive expression of heterologous genes. See generally, O'Reilly ET AL., BACULOVIRUS EXPRESSION VECTORS: A LABORATORY MANUAL (1992). Prior to inserting the foreign gene into the baculovirus genome, the above-described components, comprising a promoter, leader (if desired), coding sequence of interest, and transcription termination sequence, are typically assembled into an intermediate transplacement construct (transfer vector). Intermediate transplacement constructs are often maintained in a replicon, such as an extra chromosomal element (e.g., plasmids) capable of stable maintenance in a host, such as bacteria. The replicon will have a replication system, thus allowing it to be maintained in a suitable host for cloning and amplification. More specifically, the plasmid may contain the polyhedrin polyadenylation signal (Miller, ANN. REV. MICROBIOL. (1988) 42:177) and a prokaryotic ampicillin-resistance (amp) gene and origin of replication for selection and propagation in E. coli. One commonly used transfer vector for introducing foreign genes into AcNPV is pAc373. Many other vectors, known to those of skill in the art, have also been designed including, for example, pVL985, which alters the polyhedrin start codon from ATG to ATT, and which introduces a BamHI cloning site 32 base pairs downstream from the ATT. See Luckow and Summers, VIROLOGY 170:31 (1989). Other commercially available vectors include, for example, PBlueBac4.5/V5-His; pBlueBacHis2; pMelBac; pBlueBac4.5 (Invitrogen Corp., Carlsbad, Calif.). After insertion of the heterologous gene, the transfer vector and wild type baculoviral genome are co-transfected into an insect cell host. Methods for introducing heterologous DNA into the desired site in the baculovirus virus are known in the art. See SUMMERS AND SMITH, TEXAS AGRICULTURAL EXPERIMENT STATION BULLETIN NO. 1555 (1987); Smith et al., MOL. CELL. BIOL. (1983) 3:2156; Luckow and Summers, VIROLOGY (1989) 170:31. For example, the insertion can be into a gene such as the polyhedrin gene, by homologous double crossover recombination; insertion can also be into a restriction enzyme site engineered into the desired baculovirus gene. See Miller et al., BIOESSAYS (1989) 11(4):91. Transfection may be accomplished by electroporation. See TROTTER AND WOOD, 39 METHODS IN MOLECULAR BIOLOGY (1995); Mann and King, J. GEN. VIROL. (1989) 70:3501. Alternatively, liposomes may be used to transfect the insect cells with the recombinant expression vector and the baculovirus. See, e.g., Liebman et al., BIOTECHNIQUES (1999) 26(1):36; Graves et al., BIOCHEMISTRY (1998) 37:6050; Nomura et al., J. BIOL. CHEM. (1998) 273(22):13570; Schmidt et al., PROTEIN EXPRESSION AND PURIFICATION (1998) 12:323; Siffert et al., NATURE GENETICS (1998) 18:45; TILKINS ET AL., CELL BIOLOGY: A LABORATORY HANDBOOK 145-154 (1998); Cai et al., PROTEIN EXPRESSION AND PURIFICATION (1997) 10:263; Dolphin et al., NATURE GENETICS (1997) 17:491; Kost et al., GENE (1997) 190:139; Jakobsson et al., J. BIOL. CHEM. (1996) 271:22203; Rowles et al., J. BIOL. CHEM. (1996) 271(37):22376; Reverey et al., J. BIOL. CHEM. (1996) 271(39):23607-10; Stanley et al., J. BIOL. CHEM. (1995) 270:4121; Sisk et al., J. VIROL. (1994) 68(2):766; and Peng et al., BIOTECHNIQUES (1993) 14(2):274. Commercially available liposomes include, for example, Cellfectin� and Lipofectin� (Invitrogen, Corp., Carlsbad, Calif.). In addition, calcium phosphate transfection may be used. See T ROTTER AND WOOD, 39 METHODS IN MOLECULAR BIOLOGY (1995); Kitts, NAR (1990) 18(19):5667; and Mann and King, J. GEN. VIROL. (1989) 70:3501. Baculovirus expression vectors usually contain a baculovirus promoter. A baculovirus promoter is any DNA sequence capable of binding a baculovirus RNA polymerase and initiating the downstream (3′) transcription of a coding sequence (e.g., structural gene) into mRNA. A promoter will have a transcription initiation region which is usually placed proximal to the 5′ end of the coding sequence. This transcription initiation region typically includes an RNA polymerase binding site and a transcription initiation site. A baculovirus promoter may also have a second domain called an enhancer, which, if present, is usually distal to the structural gene. Moreover, expression may be either regulated or constitutive. Structural genes, abundantly transcribed at late times in the infection cycle, provide particularly useful promoter sequences. Examples include sequences derived from the gene encoding the viral polyhedron protein (FRIESEN ET AL., The Regulation of Baculovirus Gene Expression in THE MOLECULAR BIOLOGY OF BACULOVIRUSES (1986); EP 0 127 839 and 0 155 476) and the gene encoding the p10 protein (Vlak et al., J. GEN. VIROL. (1988) 69:765). The newly formed baculovirus expression vector is packaged into an infectious recombinant baculovirus and subsequently grown plaques may be purified by techniques known to those of ordinary skill in the art. See Miller et al., BIOESSAYS (1989) 11(4):91; SUMMERS AND SMITH, TEXAS AGRICULTURAL EXPERIMENT STATION BULLETIN NO. 1555 (1987). Recombinant baculovirus expression vectors have been developed for infection into several insect cells. For example, recombinant baculoviruses have been developed for, inter alia, Aedes aegypti (ATCC No. CCL-125), Bombyx mori (ATCC No. CRL-8910), Drosophila melanogaster (ATCC No. 1963), Spodoptera frugiperda, and Trichoplusia ni. See Wright, NATURE (1986) 321:718; Carbonell et al., J. VIROL. (1985) 56:153; Smith et al., MOL. CELL. BIOL. (1983) 3:2156. See generally, Fraser et al., IN VITRO CELL. DEV. BIOL. (1989) 25:225. More specifically, the cell lines used for baculovirus expression vector systems commonly include, but are not limited to, Sf9 (Spodoptera frugiperda) (ATCC No. CRL-1711), Sf21 (Spodoptera frugiperda) (Invitrogen Corp., Cat. No. 11497-013 (Carlsbad, Calif.)), Tri-368 (Trichopulsia ni), and High-Five� BTI-TN-5B1-4 (Trichopulsia ni). Cells and culture media are commercially available for both direct and fusion expression of heterologous polypeptides in a baculovirus/expression, and cell culture technology is generally known to those of ordinary skill in the art. E. Coli. Pseudomonas species, and other Prokaryotes Bacterial expression techniques are known to those of ordinary skill in the art. A wide variety of vectors are available for use in bacterial hosts. The vectors may be single copy or low or high multicopy vectors. Vectors may serve for cloning and/or expression. In view of the ample literature concerning vectors, commercial availability of many vectors, and even manuals describing vectors and their restriction maps and characteristics, no extensive discussion is required here. As is well-known, the vectors normally involve markers allowing for selection, which markers may provide for cytotoxic agent resistance, prototrophy or immunity. Frequently, a plurality of markers is present, which provide for different characteristics. A bacterial promoter is any DNA sequence capable of binding bacterial RNA polymerase and initiating the downstream (3′) transcription of a coding sequence (e.g. structural gene) into mRNA. A promoter will have a transcription initiation region which is usually placed proximal to the 5′ end of the coding sequence. This transcription initiation region typically includes an RNA polymerase binding site and a transcription initiation site. A bacterial promoter may also have a second domain called an operator that may overlap an adjacent RNA polymerase binding site at which RNA synthesis begins. The operator permits negative regulated (inducible) transcription, as a gene repressor protein may bind the operator and thereby inhibit transcription of a specific gene. Constitutive expression may occur in the absence of negative regulatory elements, such as the operator. In addition, positive regulation may be achieved by a gene activator protein binding sequence, which, if present is usually proximal (5′) to the RNA polymerase binding sequence. An example of a gene activator protein is the catabolite activator protein (CAP), which helps initiate transcription of the lac operon in Escherichia coli (E. coli) [Raibaud et al., ANNU. REV. GENET. (1984) 18:173]. Regulated expression may therefore be either positive or negative, thereby either enhancing or reducing transcription. Sequences encoding metabolic pathway enzymes provide particularly useful promoter sequences. Examples include promoter sequences derived from sugar metabolizing enzymes, such as galactose, lactose (lac) [Chang et al., NATURE (1977) 198:1056], and maltose. Additional examples include promoter sequences derived from biosynthetic enzymes such as tryptophan (trp) [Goeddel et al., NUC. ACIDS RES. (1980) 8:4057; Yelverton et al., NUCL. ACIDS RES. (1981) 9:731; U.S. Pat. No. 4,738,921; EP Pub. Nos. 036 776 and 121 775, which are incorporated by reference herein]. The β-galactosidase (bla) promoter system [Weissmann (1981) �The cloning of interferon and other mistakes.� In Interferon 3 (Ed. I. Gresser)], bacteriophage lambda PL [Shimatake et al., NATURE (1981) 292:128] and T5 [U.S. Pat. No. 4,689,406, which are incorporated by reference herein] promoter systems also provide useful promoter sequences. Strong promoters, such as the T7 promoter may be used to induce the polypeptide of interest at high levels. Examples of such vectors are known to those of ordinary skill in the art and include the pET29 series from Novagen, and the pPOP vectors described in WO99/05297, which is incorporated by reference herein. Such expression systems produce high levels of polypeptide in the host without compromising host cell viability or growth parameters. pET19 (Novagen) is another vector known in the art. In addition, synthetic promoters which do not occur in nature also function as bacterial promoters. For example, transcription activation sequences of one bacterial or bacteriophage promoter may be joined with the operon sequences of another bacterial or bacteriophage promoter, creating a synthetic hybrid promoter [U.S. Pat. No. 4,551,433, which is incorporated by reference herein]. For example, the tac promoter is a hybrid trp-lac promoter comprised of both trp promoter and lac operon sequences that is regulated by the lac repressor [Amann et al., GENE (1983) 25:167; de Boer et al., PROC. NATL. ACAD. SCI. (1983) 80:21]. Furthermore, a bacterial promoter can include naturally occurring promoters of non-bacterial origin that have the ability to bind bacterial RNA polymerase and initiate transcription. A naturally occurring promoter of non-bacterial origin can also be coupled with a compatible RNA polymerase to produce high levels of expression of some genes in prokaryotes. The bacteriophage T7 RNA polymerase/promoter system is an example of a coupled promoter system [Studier et al., J. MOL. BIOL. (1986) 189:113; Tabor et al., Proc Natl. Acad. Sci. (1985) 82:1074]. In addition, a hybrid promoter can also be comprised of a bacteriophage promoter and an E. coli operator region (EP Pub. No. 267 851). In addition to a functioning promoter sequence, an efficient ribosome binding site is also useful for the expression of foreign genes in prokaryotes. In E. coli, the ribosome binding site is called the Shine-Dalgarno (SD) sequence and includes an initiation codon (ATG) and a sequence 3-9 nucleotides in length located 3-11 nucleotides upstream of the initiation codon [Shine et al., NATURE (1975) 254:34]. The SD sequence is thought to promote binding of mRNA to the ribosome by the pairing of bases between the SD sequence and the 3′ and of E. coli 16S rRNA [Steitz et al. �Genetic signals and nucleotide sequences in messenger RNA�, In Biological Regulation and Development: Gene Expression (Ed. R. F. Goldberger, 1979)]. To express eukaryotic genes and prokaryotic genes with weak ribosome-binding site [Sambrook et al. �Expression of cloned genes in Escherichia coli�, Molecular Cloning: A Laboratory Manual, 1989]. The term �bacterial host� or �bacterial host cell� refers to a bacterial that can be, or has been, used as a recipient for recombinant vectors or other transfer DNA. The term includes the progeny of the original bacterial host cell that has been transfected. It is understood that the progeny of a single parental cell may not necessarily be completely identical in morphology or in genomic or total DNA complement to the original parent, due to accidental or deliberate mutation. Progeny of the parental cell that are sufficiently similar to the parent to be characterized by the relevant property, such as the presence of a nucleotide sequence encoding a polypeptide of interest, are included in the progeny intended by this definition. The selection of suitable host bacteria for expression of polypeptides is known to those of ordinary skill in the art. In selecting bacterial hosts for expression, suitable hosts may include those shown to have, inter alia, good inclusion body formation capacity, low proteolytic activity, and overall robustness. Bacterial hosts are generally available from a variety of sources including, but not limited to, the Bacterial Genetic Stock Center, Department of Biophysics and Medical Physics, University of California (Berkeley, Calif.); and the American Type Culture Collection (�ATCC�) (Manassas, Va.). Industrial/pharmaceutical fermentation generally use bacterial derived from K strains (e.g. W3110) or from bacteria derived from B strains (e.g. BL21). These strains are particularly useful because their growth parameters are extremely well known and robust. In addition, these strains are non-pathogenic, which is commercially important for safety and environmental reasons. Other examples of suitable E. coli hosts include, but are not limited to, strains of BL21, DH10B, or derivatives thereof. In another embodiment of the methods of the present invention, the E. coli host is a protease minus strain including, but not limited to, OMP- and LON-. The host cell strain may be a species of Pseudomonas, including but not limited to, Pseudomonas fluorescens, Pseudomonas aeruginosa, and Pseudomonas putida. Pseudomonas fluorescens biovar 1, designated strain MB101, is known to be useful for recombinant production and is available for therapeutic protein production processes. Examples of a Pseudomonas expression system include the system available from The Dow Chemical Company as a host strain (Midland, Mich. available on the World Wide Web at dow.com). U.S. Pat. Nos. 4,755,465 and 4,859,600, which are incorporated by reference herein, describe the use of Pseudomonas strains as a host cell for hGH production. Once a recombinant host cell strain has been established (i.e., the expression construct has been introduced into the host cell and host cells with the proper expression construct are isolated), the recombinant host cell strain is cultured under conditions appropriate for production of the polypeptide of interest. As will be apparent to one of skill in the art, the method of culture of the recombinant host cell strain will be dependent on the nature of the expression construct utilized and the identity of the host cell. Recombinant host strains are normally cultured using methods that are well known to the art. Recombinant host cells are typically cultured in liquid medium containing assimilatable sources of carbon, nitrogen, and inorganic salts and, optionally, containing vitamins, amino acids, growth factors, and other proteinaceous culture supplements known to those of ordinary skill in the art. Liquid media for culture of host cells may optionally contain antibiotics or anti-fungals to prevent the growth of undesirable microorganisms and/or compounds including, but not limited to, antibiotics to select for host cells containing the expression vector. Recombinant host cells may be cultured in batch or continuous formats, with either cell harvesting (in the case where the polypeptide of interest accumulates intracellularly) or harvesting of culture supernatant in either batch or continuous formats. For production in prokaryotic host cells, batch culture and cell harvest are preferred. Selector Codons Selector codons of the present invention expand the genetic codon framework of protein biosynthetic machinery. For example, a selector codon includes, e.g., a unique three base codon, a nonsense codon, such as a stop codon, including but not limited to, an amber codon (UAG), an ochre codon, or an opal codon (UGA), an unnatural codon, a four base (or more) codon, a rare codon, or the like. A number of selector codons can be introduced into a desired gene or polynucleotide, e.g., one or more, two or more, three or more, etc. In one embodiment, the methods involve the use of a selector codon that is a stop codon for the incorporation of a selected amino acid, e.g., an unnatural amino acid, in vivo. For example, an O-tRNA is produced that recognizes the stop codon and is aminoacylated by an O-RS with a selected amino acid. This O-tRNA is not recognized by the naturally occurring host's aminoacyl-tRNA synthetases. Conventional site-directed mutagenesis can be used to introduce the stop codon at the site of interest in a polypeptide of interest. See, e.g., Sayers, J. R., et al. (1988), 5′-3′ Exonucleases in phosphorothioate-based oligonucleotide-directed mutagenesis. Nucleic Acids Res, 16:791-802. When the O-RS, O-tRNA and the nucleic acid that encodes a polypeptide of interest are combined, e.g., in vivo, the selected amino acid is incorporated in response to the stop codon to give a polypeptide containing the selected amino acid, e.g., an unnatural amino acid, at the specified position. In one embodiment of the present invention, a stop codon used as a selector codon is an amber codon, UAG, and/or an opal codon, UGA. For example, see SEQ ID NO.: 6 for an example of an O-tRNA that recognizes an amber codon, and see SEQ ID NO.: 7 for an example of an O-tRNA that recognizes an opal codon. A genetic code in which UAG and UGA are both used as a selector codon can encode 22 amino acids while preserving the ochre nonsense codon, UAA, which is the most abundant termination signal. The incorporation of selected amino acids, e.g., unnatural amino acids, in vivo can be done without significant perturbation of the host cell. For example in non-eukaryotic cells, such as Escherichia coli, because the suppression efficiency for the UAG codon depends upon the competition between the O-tRNA, e.g., the amber suppressor tRNA, and the release factor 1 (RF1) (which binds to the UAG codon and initiates release of the growing peptide from the ribosome), the suppression efficiency can be modulated by, e.g., either increasing the expression level of O-tRNA, e.g., the suppressor tRNA, or using an RF1 deficient strain. In eukaryotic cells, because the suppression efficiency for the UAG codon depends upon the competition between the O-tRNA, e.g., the amber suppressor tRNA, and a eukaryotic release factor (e.g., eRF) (which binds to a stop codon and initiates release of the growing peptide from the ribosome), the suppression efficiency can be modulated by, e.g., increasing the expression level of O-tRNA, e.g., the suppressor tRNA. Unnatural amino acids can also be encoded with rare codons. For example, when the arginine concentration in an in vitro protein synthesis reaction is reduced, the rare arginine codon, AGG, has proven to be efficient for insertion of Ala by a synthetic tRNA acylated with alanine. See, e.g., Ma et al., Biochemistry, 32:7939 (1993). In this case, the synthetic tRNA competes with the naturally occurring tRNAArg, which exists as a minor species in Escherichia coli. Some organisms do not use all triplet codons. An unassigned codon AGA in Micrococcus luteus has been utilized for insertion of amino acids in an in vitro transcription/translation extract. See, e.g., Kowal and Oliver, Nucl. Acid. Res., 25:4685 (1997). Components of the present invention can be generated to use these rare codons in vivo. Selector codons also comprise extended codons, e.g., four or more base codons, such as, four, five, six or more base codons. Examples of four base codons include but are not limited to, AGGA, CUAG, UAGA, CCCU, and the like. Examples of five base codons include but are not limited to, AGGAC, CCCCU, CCCUC, CUAGA, CUACU, UAGGC and the like. A feature may include using extended codons based on frameshift suppression. Four or more base codons can insert, e.g., one or multiple selected amino acids, including but not limited to, unnatural amino acids, into the same protein. For example, in the presence of mutated O-tRNA's, e.g., a special frameshift suppressor tRNA's, with anticodon loops, e.g., with a CU(X)n XXXAA sequence (where n=1), the four or more base codon is read as single amino acid. For example, see SEQ ID NOs.: 6, 12 from PCT/US04/22061 for O-tRNA's that recognize a four base codon. In other embodiments, the anticodon loops can decode, e.g., at least a four-base codon, at least a five-base codon, or at least a six-base codon or more. Since there are 256 possible four-base codons, multiple unnatural amino acids can be encoded in the same cell using a four or more base codon. See, Anderson et al., (2002) Exploring the Limits of Codon and Anticodon Size, Chemistry and Biology, 9:237-244; Magliery, (2001) Expanding the Genetic Code: Selection of Efficient Suppressors of Four-base Codons and Identification of �Shifty� Four-base Codons with a Library Approach in Escherichia coli, J. Mol. Biol. 307: 755-769. For example, four-base codons have been used to incorporate unnatural amino acids into proteins using in vitro biosynthetic methods. See, e.g., Ma et al., (1993) Biochemistry, 32:7939; and Hohsaka et al., (1999) J. Am. Chem. Soc., 121:34. CGGG and AGGU were used to simultaneously incorporate 2-naphthylalanine and an NBD derivative of lysine into streptavidin in vitro with two chemically acylated frameshift suppressor tRNA's. See, e.g., Hohsaka et al., (1999) J. Am. Chem. Soc., 121:12194. In an in vivo study, Moore et al. examined the ability of tRNALeu derivatives with NCUA anticodons to suppress UAGN codons (N can be U, A, G, or C), and found that the quadruplet UAGA can be decoded by a tRNALeu with a UCUA anticodon with an efficiency of 13 to 26% with little decoding in the 0 or −1 frame. See, Moore et al., (2000) J. Mol. Biol., 298:195. In one embodiment, extended codons based on rare codons or nonsense codons can be used in invention, which can reduce missense readthrough and frameshift suppression at other unwanted sites. For a given system, a selector codon can also include one of the natural three base codons, where the endogenous system does not use (or rarely uses) the natural base codon. For example, this includes a system that is lacking a tRNA that recognizes the natural three base codon, and/or a system where the three base codon is a rare codon. Selector codons optionally include unnatural base pairs. These unnatural base pairs further expand the existing genetic alphabet. One extra base pair increases the number of triplet codons from 64 to 125. Properties of third base pairs include stable and selective base pairing, efficient enzymatic incorporation into DNA with high fidelity by a polymerase, and the efficient continued primer extension after synthesis of the nascent unnatural base pair. Descriptions of unnatural base pairs which can be adapted for methods and compositions include, e.g., Hirao, et al., (2002) An unnatural base pair for incorporating amino acid analogues into protein, Nature Biotechnology, 20:177-182. See, also, Wu, Y., et al., (2002) J. Am. Chem. Soc. 124:14626-14630. Other relevant publications are listed below. For in vivo usage, the unnatural nucleoside is membrane permeable and is phosphorylated to form the corresponding triphosphate. In addition, the increased genetic information is stable and not destroyed by cellular enzymes. Previous efforts by Benner and others took advantage of hydrogen bonding patterns that are different from those in canonical Watson-Crick pairs, the most noteworthy example of which is the iso-C:iso-G pair. See, e.g., Switzer et al., (1989) J. Am. Chem. Soc., 111:8322; and Piccirilli et al., (1990) Nature, 343:33; Kool, (2000) Curr. Opin. Chem. Biol., 4:602. These bases in general mispair to some degree with natural bases and cannot be enzymatically replicated. Kool and co-workers demonstrated that hydrophobic packing interactions between bases can replace hydrogen bonding to drive the formation of base pair. See, Kool, (2000) Curr. Opin. Chem. Biol., 4:602; and Guckian and Kool, (1998) Angew. Chem. Int. Ed. Engl., 36, 2825. In an effort to develop an unnatural base pair satisfying all the above requirements, Schultz, Romesberg and co-workers have systematically synthesized and studied a series of unnatural hydrophobic bases. A PICS:PICS self-pair is found to be more stable than natural base pairs, and can be efficiently incorporated into DNA by Klenow fragment of Escherichia coli DNA polymerase I (KF). See, e.g., McMinn et al., (1999) J. Am. Chem. Soc., 121:11585-6; and Ogawa et al., (2000) J. Am. Chem. Soc., 122:3274. A 3MN:3MN self-pair can be synthesized by KF with efficiency and selectivity sufficient for biological function. See, e.g., Ogawa et al., (2000) J. Am. Chem. Soc. 122:8803. However, both bases act as a chain terminator for further replication. A mutant DNA polymerase has been recently evolved that can be used to replicate the PICS self pair. In addition, a 7AI self pair can be replicated. See, e.g., Tae et al., (2001) J. Am. Chem. Soc., 123:7439. A novel metallobase pair, Dipic:Py, has also been developed, which forms a stable pair upon binding Cu(II). See, Meggers et al., (2000) J. Am. Chem. Soc., 122:10714. Because extended codons and unnatural codons are intrinsically orthogonal to natural codons, the methods of the present invention can take advantage of this property to generate orthogonal tRNAs for them. A translational bypassing system can also be used to incorporate a selected amino acid, e.g., an unnatural amino acid, in a desired polypeptide. In a translational bypassing system, a large sequence is inserted into a gene but is not translated into protein. The sequence contains a structure that serves as a cue to induce the ribosome to hop over the sequence and resume translation downstream of the insertion. Selected and Unnatural Amino Acids As used herein, a selected amino acid refers to any desired naturally occurring amino acid or unnatural amino acid. A naturally occurring amino acid includes any one of the twenty genetically encoded alpha-amino acids: alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine. In one embodiment, the selected amino acid is incorporated into a growing polypeptide chain with high fidelity, e.g., at greater than about 70% efficiency for given selector codon, at greater than 75% efficiency for a given selector codon, at greater than about 80% efficiency for a given selector codon, at greater than about 85% efficiency for a given selector codon, at greater than about 90% efficiency for a given selector codon, at greater than about 95% efficiency for a given selector codon, or at greater than about 99% or more efficiency for a given selector codon. As used herein, an unnatural amino acid refers to any amino acid, modified amino acid, or amino acid analogue other than selenocysteine and/or pyrrolysine and the following twenty genetically encoded alpha-amino acids: alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, valine. The generic structure of an alpha-amino acid is illustrated by Formula I: An unnatural amino acid is typically any structure having Formula I wherein the R group is any substituent other than one used in the twenty natural amino acids. See, e.g., Biochemistry by L. Stryer, 3rd ed. 1988, Freeman and Company, New York, for structures of the twenty natural amino acids. Note that, the unnatural amino acids of the present invention can be naturally occurring compounds other than the twenty alpha-amino acids above. Because the unnatural amino acids of the present invention typically differ from the natural amino acids only in the structure of the side chain, the unnatural amino acids form amide bonds with other amino acids, including but not limited to, natural or unnatural, in the same manner in which they are formed in naturally occurring proteins. However, the unnatural amino acids have side chain groups that distinguish them from the natural amino acids. For example, R in Formula I may comprise an alkyl-, aryl-, acyl-, keto-, azido-, hydroxyl-, hydrazine, cyano-, halo-, hydrazide, alkenyl, alkynl, ether, thiol, seleno-, sulfonyl-, borate, boronate, phospho, phosphono, phosphine, heterocyclic, enone, imine, aldehyde, ester, thioacid, hydroxylamine, amine, and the like, or any combination thereof. Other non-naturally occurring amino acids include, but are not limited to, amino acids comprising a photoactivatable cross-linker, spin-labeled amino acids, fluorescent amino acids, metal binding amino acids, metal-containing amino acids, radioactive amino acids, amino acids with novel functional groups, amino acids that covalently or noncovalently interact with other molecules, photocaged and/or photoisomerizable amino acids, amino acids comprising biotin or a biotin analogue, glycosylated amino acids such as a sugar substituted serine, other carbohydrate modified amino acids, keto-containing amino acids, amino acids comprising polyethylene glycol or polyether, heavy atom substituted amino acids, chemically cleavable and/or photocleavable amino acids, amino acids with an elongated side chains as compared to natural amino acids, including but not limited to, polyethers or long chain hydrocarbons, including but not limited to, greater than about 5 or greater than about 10 carbons, carbon-linked sugar-containing amino acids, redox-active amino acids, amino thioacid containing amino acids, and amino acids comprising one or more toxic moiety. See, also, U.S. Patent Application Publications 2003/0082575 and 2003/0108885, which are incorporated by reference herein. Unnatural amino acids may have a photoactivatable cross-linker that is used, e.g., to link a protein to a solid support. Unnatural amino acids may have a saccharide moiety attached to the amino acid side chain. In addition to unnatural amino acids that contain novel side chains, unnatural amino acids also optionally comprise modified backbone structures, e.g., as illustrated by the structures of Formula II and III: wherein Z typically comprises OH, NH2, SH, NH�R′, or S�R′; X and Y, which can be the same or different, typically comprise S or O, and R and R′, which are optionally the same or different, are typically selected from the same list of constituents for the R group described above for the unnatural amino acids having Formula I as well as hydrogen. For example, unnatural amino acids may comprise substitutions in the amino or carboxyl group as illustrated by Formulas II and III. Unnatural amino acids of this type include, but are not limited to, α-hydroxy acids, α-thioacids, α-aminothiocarboxylates, e.g., with side chains corresponding to the common twenty natural amino acids or unnatural side chains. In addition, substitutions at the α-carbon optionally include L, D, or α-α-disubstituted amino acids such as D-glutamate, D-alanine, D-methyl-O-tyrosine, aminobutyric acid, and the like. Other structural alternatives include cyclic amino acids, such as proline analogues as well as 3, 4, 6, 7, 8, and 9 membered ring proline analogues, β and γ amino acids such as substituted β-alanine and γ-amino butyric acid. Many unnatural amino acids are based on natural amino acids, such as tyrosine, glutamine, phenylalanine, and the like. Tyrosine analogs include para-substituted tyrosines, ortho-substituted tyrosines, and meta substituted tyrosines, wherein the substituted tyrosine comprises a keto group (including but not limited to, an acetyl group), a benzoyl group, an amino group, a hydrazine, an hydroxyamine, a thiol group, a carboxy group, an isopropyl group, a methyl group, a C6-C20 straight chain or branched hydrocarbon, a saturated or unsaturated hydrocarbon, an O-methyl group, a polyether group, a nitro group, or the like. In addition, multiply substituted aryl rings are also contemplated. Glutamine analogs include, but are not limited to, α-hydroxy derivatives, γ-substituted derivatives, cyclic derivatives, and amide substituted glutamine derivatives. Example phenylalanine analogs include, but are not limited to, para-substituted phenylalanines, ortho-substituted phenylalanines, and meta-substituted phenylalanines, wherein the substituent comprises a hydroxy group, a methoxy group, a methyl group, an allyl group, an aldehyde, an azido, an iodo, a bromo, a keto group (including but not limited to, an acetyl group), or the like. Specific examples of unnatural amino acids include, but are not limited to, a p-acetyl-L-phenylalanine, a p-propargyl-phenylalanine, O-methyl-L-tyrosine, an L-3-(2-naphthyl)alanine, a 3-methyl-phenylalanine, an O-4-allyl-L-tyrosine, a 4-propyl-L-tyrosine, a tri-O-acetyl-GlcNAcβ-serine, an L-Dopa, a fluorinated phenylalanine, an isopropyl-L-phenylalanine, a p-azido-L-phenylalanine, a p-acyl-L-phenylalanine, a p-benzoyl-L-phenylalanine, an L-phosphoserine, a phosphonoserine, a phosphonotyrosine, a p-iodo-phenylalanine, a p-bromophenylalanine, a p-amino-L-phenylalanine, an isopropyl-L-phenylalanine, and a p-propargyloxy-phenylalanine, and the like. Examples of structures of a variety of unnatural amino acids are provided in, for example, WO 2002/085923 entitled �In vivo incorporation of unnatural amino acids,� which is incorporated by reference herein. See also Kiick et al., (2002) Incorporation of azides into recombinant proteins for chemoselective modification by the Staudinger ligation, PNAS 99:19-24, which is incorporated by reference herein, for additional methionine analogs. A non-natural amino acid incorporated into a polypeptide at the amino terminus can be composed of an R group that is any substituent other than one used in the twenty natural amino acids and a 2nd reactive group different from the NH2 group normally present in α-amino acids (see Formula I). A similar non-natural amino acid can be incorporated at the carboxyl terminus with a 2nd reactive group different from the COOH group normally present in α-amino acids (see Formula I). The unnatural amino acids of the invention may be selected or designed to provide additional characteristics unavailable in the twenty natural amino acids. For example, unnatural amino acid may be optionally designed or selected to modify the biological properties of a protein, e.g., into which they are incorporated. For example, the following properties may be optionally modified by inclusion of an unnatural amino acid into a protein: toxicity, biodistribution, solubility, stability, e.g., thermal, hydrolytic, oxidative, resistance to enzymatic degradation, and the like, facility of purification and processing, structural properties, spectroscopic properties, chemical and/or photochemical properties, catalytic activity, redox potential, half-life, ability to react with other molecules, e.g., covalently or noncovalently, and the like. The structures of a variety of unnatural amino acids are provided in, for example, FIGS. 16, 17, 18, 19, 26, and 29 of WO 2002/085923 entitled �In vivo incorporation of unnatural amino acids,� which is incorporated by reference herein. The examples are not meant to be limiting in any way of amino acids that may be attached to a tRNA of the present invention. One advantage of an unnatural amino acid is that it presents additional chemical moieties that can be used to add additional molecules. These modifications can be made in vivo in a eukaryotic or non-eukaryotic cell, or in vitro. Thus, in certain embodiments, the post-translational modification is through the unnatural amino acid. An unnatural amino acid in a polypeptide may be used to attach another molecule to the polypeptide, including but not limited to, a label, a dye, a polymer, a water-soluble polymer, a derivative of polyethylene glycol, a photocrosslinker, a radionuclide, a cytotoxic compound, a drug, an affinity label, a photoaffinity label, a reactive compound, a resin, a second protein or polypeptide or polypeptide analog, an antibody or antibody fragment, a metal chelator, a cofactor, a fatty acid, a carbohydrate, a polynucleotide, a DNA, a RNA, an antisense polynucleotide, a saccharide, a water-soluble dendrimer, a cyclodextrin, an inhibitory ribonucleic acid, a biomaterial, a nanoparticle, a spin label, a fluorophore, a metal-containing moiety, a radioactive moiety, a novel functional group, a group that covalently or noncovalently interacts with other molecules, a photocaged moiety, an actinic radiation excitable moiety, a photoisomerizable moiety, biotin, a derivative of biotin, a biotin analogue, a moiety incorporating a heavy atom, a chemically cleavable group, a photocleavable group, an elongated side chain, a carbon-linked sugar, a redox-active agent, an amino thioacid, a toxic moiety, an isotopically labeled moiety, a biophysical probe, a phosphorescent group, a chemiluminescent group, an electron dense group, a magnetic group, an intercalating group, a chromophore, an energy transfer agent, a biologically active agent, a detectable label, a small molecule, a quantum dot, a nanotransmitter, or any combination of the above or any other desirable compound or substance, comprising a second reactive group to at least one unnatural amino acid comprising a first reactive group utilizing chemistry methodology that is known to one of ordinary skill in the art to be suitable for the particular reactive groups. For example, the post-translational modification can be through a nucleophilic-electrophilic reaction. Most reactions currently used for the selective modification of proteins involve covalent bond formation between nucleophilic and electrophilic reaction partners, including but not limited to the reaction of α-haloketones with histidine or cysteine side chains. Selectivity in these cases is determined by the number and accessibility of the nucleophilic residues in the protein. In proteins of the invention, other more selective reactions can be used such as the reaction of an unnatural keto-amino acid with hydrazides or aminooxy compounds, in vitro and in vivo. See, e.g., Cornish, et al., (1996) J. Am. Chem. Soc., 118:8150-8151; Mahal, et al., (1997) Science, 276:1125-1128; Wang, et al., (2001) Science 292:498-500; Chin, et al., (2002) J. Am. Chem. Soc. 124:9026-9027; Chin, et al., (2002) Proc. Natl. Acad. Sci., 99:11020-11024; Wang, et al., (2003) Proc. Natl. Acad. Sci., 100:56-61; Zhang, et al., (2003) Biochemistry, 42:6735-6746; and, Chin, et al., (2003) Science, 301:964-7, all of which are incorporated by reference herein. This allows the selective labeling of virtually any protein with a host of reagents including fluorophores, crosslinking agents, saccharide derivatives and cytotoxic molecules. See also, U.S. Pat. No. 6,927,042 entitled �Glycoprotein synthesis,� which is incorporated by reference herein. Post-translational modifications, including but not limited to, through an azido amino acid, can also made through the Staudinger ligation (including but not limited to, with triarylphosphine reagents). See, e.g., Kiick et al., (2002) Incorporation of azides into recombinant proteins for chemoselective modification by the Staudinger ligation, PNAS 99:19-24. Chemical Synthesis of Unnatural Amino Acids Many unnatural amino acids are commercially available, e.g., from Sigma-Aldrich (St. Louis, Mo., USA), Novabiochem (a division of EMD Biosciences, Darmstadt, Germany), or Peptech (Burlington, Mass., USA). Those that are not commercially available are optionally synthesized as provided herein or using standard methods known to those of ordinary skill in the art. For organic synthesis techniques, see, e.g., Organic Chemistry by Fessendon and Fessendon, (1982, Second Edition, Willard Grant Press, Boston Mass.); Advanced Organic Chemistry by March (Third Edition, 1985, Wiley and Sons, New York); and Advanced Organic Chemistry by Carey and Sundberg (Third Edition, Parts A and B, 1990, Plenum Press, New York). Additional publications describing the synthesis of unnatural amino acids include, e.g., WO 2002/085923 entitled �In vivo incorporation of Unnatural Amino Acids;� Matsoukas et al., (1995) J. Med. Chem., 38, 4660-4669; King, F. E. & Kidd, D. A. A. (1949) A New Synthesis of Glutamine and of γ-Dipeptides of Glutamic Acid from Phthylated Intermediates. J. Chem. Soc., 3315-3319; Friedman, O. M. & Chatterrji, R. (1959) Synthesis of Derivatives of Glutamine as Model Substrates for Anti-Tumor Agents. J. Am. Chem. Soc. 81, 3750-3752; Craig, J. C. et al. (1988) Absolute Configuration of the Enantiomers of 7-Chloro-4 [[4-(diethylamino)-1-methylbutyl]amino]quinoline (Chloroquine). J. Org. Chem. 53, 1167-1170; Azoulay, M., Vilmont, M. & Frappier, F. (1991) Glutamine analogues as Potential Antimalarials, Eur. J. Med. Chem. 26, 201-5; Koskinen, A. M. P. & Rapoport, H. (1989) Synthesis of 4-Substituted Prolines as Conformationally Constrained Amino Acid Analogues. J. Org. Chem. 54, 1859-1866; Christie, B. D. & Rapoport, H. (1985) Synthesis of Optically Pure Pipecolates from L-Asparagine. Application to the Total Synthesis of (+)-Apovincamine through Amino Acid Decarbonylation and Iminium Ion Cyclization. J. Org. Chem. 50:1239-1246; Barton et al., (1987) Synthesis of Novel alpha-Amino-Acids and Derivatives Using Radical Chemistry: Synthesis of L- and D-alpha-Amino-Adipic Acids, L-alpha-aminopimelic Acid and Appropriate Unsaturated Derivatives. Tetrahedron 43:4297-4308; and, Subasinghe et al., (1992) Quisqualic acid analogues: synthesis of beta-heterocyclic 2-aminopropanoic acid derivatives and their activity at a novel quisqualate-sensitized site. J. Med. Chem. 35:4602-7. See also, U.S. Patent Publication No. US 2004/0198637 entitled �Protein Arrays,� which is incorporated by reference. Cellular Uptake of Unnatural Amino Acids Unnatural amino acid uptake by a cell is one issue that is typically considered when designing and selecting unnatural amino acids, e.g., for incorporation into a protein. For example, the high charge density of α-amino acids suggests that these compounds are unlikely to be cell permeable. Natural amino acids are taken up into the cell via a collection of protein-based transport systems. A rapid screen can be done which assesses which unnatural amino acids, if any, are taken up by cells. See, e.g., the toxicity assays in, e.g., U.S. Patent Publication No. US 2004/0198637 entitled �Protein Arrays� which is incorporated by reference herein, and Liu, D. R. & Schultz, P. G. (1999) Progress toward the evolution of an organism with an expanded genetic code. PNAS United States 96:4780-4785. Although uptake is easily analyzed with various assays, an alternative to designing unnatural amino acids that are amenable to cellular uptake pathways is to provide biosynthetic pathways to create amino acids in vivo. Biosynthesis of Unnatural Amino Acids Many biosynthetic pathways already exist in cells for the production of amino acids and other compounds. While a biosynthetic method for a particular unnatural amino acid may not exist in nature, including but not limited to, in a cell, the invention provides such methods. For example, biosynthetic pathways for unnatural amino acids are optionally generated in host cell by adding new enzymes or modifying existing host cell pathways. Additional new enzymes are optionally naturally occurring enzymes or artificially evolved enzymes. For example, the biosynthesis of p-aminophenylalanine (as presented in an example in WO 2002/085923 entitled �In vivo incorporation of unnatural amino acids�) relies on the addition of a combination of known enzymes from other organisms. The genes for these enzymes can be introduced into a cell by transforming the cell with a plasmid comprising the genes. The genes, when expressed in the cell, provide an enzymatic pathway to synthesize the desired compound. Examples of the types of enzymes that are optionally added are provided in the examples below. Additional enzymes sequences are found, for example, in Genbank. Artificially evolved enzymes are also optionally added into a cell in the same manner. In this manner, the cellular machinery and resources of a cell are manipulated to produce unnatural amino acids. A variety of methods are available for producing novel enzymes for use in biosynthetic pathways or for evolution of existing pathways. For example, recursive recombination, e.g., as developed by Maxygen, Inc. (available on the World Wide Web at maxygen.com), is optionally used to develop novel enzymes and pathways. See, e.g., Stemmer (1994), Rapid evolution of a protein in vitro by DNA shuffling, Nature 370(4):389-391; and, Stemmer, (1994), DNA shuffling by random fragmentation and reassembly: In vitro recombination for molecular evolution, Proc. Natl. Acad. Sci. USA., 91:10747-10751. Similarly DesignPath�, developed by Genencor (available on the World Wide Web at genencor.com) is optionally used for metabolic pathway engineering, e.g., to engineer a pathway to create O-methyl-L-tyrosine in a cell. This technology reconstructs existing pathways in host organisms using a combination of new genes, including but not limited to, those identified through functional genomics, and molecular evolution and design. Diversa Corporation (available on the World Wide Web at diversa.com) also provides technology for rapidly screening libraries of genes and gene pathways, including but not limited to, to create new pathways. Typically, the unnatural amino acid produced with an engineered biosynthetic pathway of the present invention is produced in a concentration sufficient for efficient protein biosynthesis, e.g., a natural cellular amount, but not to such a degree as to affect the concentration of the other amino acids or exhaust cellular resources. Typical concentrations produced in vivo in this manner are about 10 mM to about 0.05 mM. Once a cell is transformed with a plasmid comprising the genes used to produce enzymes desired for a specific pathway and an unnatural amino acid is generated, in vivo selections are optionally used to further optimize the production of the unnatural amino acid for both ribosomal protein synthesis and cell growth. Nucleic Acid and Polypeptide Sequence and Variants As described above and below, the invention provides for nucleic acid polynucleotide sequences and polypeptide amino acid sequences, e.g., tRNA's and RSs, and, e.g., compositions and methods comprising said sequences. Examples of said sequences, e.g., tRNA's and RSs are disclosed herein. However, one of skill in the art will appreciate that the invention is not limited to those sequences disclosed herein, e.g., the Examples. One of skill will appreciate that the invention also provides many related and unrelated sequences with the functions described herein, e.g., encoding an O-tRNA or an O-RS. The invention provides polypeptides (O-RSs) and polynucleotides, e.g., O-tRNA, polynucleotides that encode O-RSs or portions thereof, oligonucleotides used to isolate aminoacyl-tRNA synthetase clones, etc. Polynucleotides of the present invention include those that encode proteins or polypeptides of interests of the present invention with one or more selector codon. In addition, polynucleotides of the present invention include, e.g., a polynucleotide comprising a nucleotide sequence as set forth in any one of SEQ ID NO.: 1, 2, 3; a polynucleotide that is complementary to, or a conservative variation thereof. Similarly, a nucleic acid that hybridizes to a polynucleotide indicated above under highly stringent conditions over substantially the entire length of the nucleic acid is a polynucleotide of the present invention. In certain embodiments, a vector (e.g., a plasmid, a cosmid, a phage, a bacterium, a virus, a naked polynucleotide, a conjugated polynucleotide, etc.) comprises a polynucleotide of the present invention. In one embodiment, the vector is an expression vector. In another embodiment, the expression vector includes a promoter operably linked to one or more of the polynucleotides of the present invention. In another embodiment, a cell comprises a vector that includes a polynucleotide of the present invention. One of skill will also appreciate that many variants of the disclosed sequences are included in the invention. For example, conservative variations of the disclosed sequences that yield a functionally identical sequence are included in the invention. Variants of the nucleic acid polynucleotide sequences, wherein the variants hybridize to at least one disclosed sequence, are considered to be included in the invention. Unique subsequences of the sequences disclosed herein, as determined by, e.g., standard sequence comparison techniques, are also included in the invention. Conservative Variations Owing to the degeneracy of the genetic code, �silent substitutions� (i.e., substitutions in a nucleic acid sequence which do not result in an alteration in an encoded polypeptide) are an implied feature of every nucleic acid sequence which encodes an amino acid. Similarly, �conservative amino acid substitutions,� in one or a few amino acids in an amino acid sequence are substituted with different amino acids with highly similar properties, are also readily identified as being highly similar to a disclosed construct. Such conservative variations of each disclosed sequence are a feature of the present invention. �Conservative variations� of a particular nucleic acid sequence refers to those nucleic acids which encode identical or essentially identical amino acid sequences, or, where the nucleic acid does not encode an amino acid sequence, to essentially identical sequences. One of ordinary skill in the art will recognize that individual substitutions, deletions or additions which alter, add or delete a single amino acid or a small percentage of amino acids in an encoded sequence are �conservatively modified variations� or �conservatively modified variants� where the alterations result in the deletion of an amino acid, addition of an amino acid, or substitution of an amino acid with a chemically similar amino acid. Thus, �conservative variations� of a listed polypeptide sequence of the present invention include substitutions of a small percentage, typically less than 5%, more typically less than 4%, 2% or 1%, of the amino acids of the polypeptide sequence, with a conservatively selected amino acid of the same conservative substitution group. The addition of sequences which do not alter the encoded activity of a nucleic acid molecule, such as the addition of a non-functional sequence, is a conservative variation of the basic nucleic acid. Conservative substitution tables providing functionally similar amino acids are known to those of ordinary skill in the art. The following eight groups each contain amino acids that are conservative substitutions for one another: 1) Alanine (A), Glycine (G); 2) Aspartic acid (D), Glutamic acid (E); 3) Asparagine (N), Glutamine (Q); 4) Arginine (R), Lysine (K); 5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); 6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W); 7) Serine (S), Threonine (T); and 8) Cysteine (C), Methionine (M) (see, e.g., Creighton, Proteins: Structures and Molecular Properties (W H Freeman & Co.; 2nd edition (December 1993) Nucleic Acid Hybridization Comparative hybridization can be used to identify nucleic acids of the present invention, such as SEQ ID NO.: 1-3, including conservative variations of nucleic acids of the present invention, and this comparative hybridization method is a preferred method of distinguishing nucleic acids of the present invention. In addition, target nucleic acids which hybridize to the nucleic acids represented by SEQ ID NO: 1-3 under high, ultra-high, and/or ultra-ultra high stringency conditions are a feature of the present invention. Examples of such nucleic acids include those with one or a few silent or conservative nucleic acid substitutions as compared to a given nucleic acid sequence. A test nucleic acid is said to specifically hybridize to a probe nucleic acid when it hybridizes at least � as well to the probe as to the perfectly matched complementary target, i.e., with a signal to noise ratio at least � as high as hybridization of the probe to the target under conditions in which the perfectly matched probe binds to the perfectly matched complementary target with a signal to noise ratio that is at least about 5�-10� as high as that observed for hybridization to any of the unmatched target nucleic acids. Nucleic acids �hybridize� when they associate, typically in solution. Nucleic acids hybridize due to a variety of well characterized physico-chemical forces, such as hydrogen bonding, solvent exclusion, base stacking and the like. The phrase �stringent hybridization conditions� refers to conditions of low ionic strength and high temperature as is known in the art. Typically, under stringent conditions a probe will hybridize to its target subsequence in a complex mixture of nucleic acid (including but not limited to, total cellular or library DNA or RNA) but does not hybridize to other sequences in the complex mixture. An extensive guide to the hybridization of nucleic acids is found in Tijssen (1993) Laboratory Techniques in Biochemistry and Molecular Biology�Hybridization with Nucleic Acid Probes part I chapter 2, �Overview of principles of hybridization and the strategy of nucleic acid probe assays,� (Elsevier, N.Y.), as well as in Ausubel et al., Current Protocols in Molecular Biology (1995). Hames and Higgins (1995) Gene Probes 1 IRL Press at Oxford University Press, Oxford, England, (Hames and Higgins 1) and Hames and Higgins (1995) Gene Probes 2 IRL Press at Oxford University Press, Oxford, England (Hames and Higgins 2) provide details on the synthesis, labeling, detection and quantification of DNA and RNA, including oligonucleotides. Generally, stringent conditions are selected to be about 5-10� C. lower than the thermal melting point (Tm) for the specific sequence at a defined ionic strength pH. The Tm is the temperature (under defined ionic strength, pH, and nucleic concentration) at which 50% of the probes complementary to the target hybridize to the target sequence at equilibrium (as the target sequences are present in excess, at Tm, 50% of the probes are occupied at equilibrium). Stringent conditions may be those in which the salt concentration is less than about 1.0 M sodium ion, typically about 0.01 to 1.0 M sodium ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30� C. for short probes (including but not limited to, 10 to 50 nucleotides) and at least about 60� C. for long probes (including but not limited to, greater than 50 nucleotides). Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide. For selective or specific hybridization, a positive signal may be at least two times background, optionally 10 times background hybridization. Exemplary stringent hybridization conditions can be as following: 50% formamide, 5�SSC, and 1% SDS, incubating at 42� C., or 5�SSC, 1% SDS, incubating at 65� C., with wash in 0.2�SSC, and 0.1% SDS at 65� C. Such washes can be performed for 5, 15, 30, 60, 120, or more minutes. An example of stringent hybridization conditions for hybridization of complementary nucleic acids which have more than 100 complementary residues on a filter in a Southern or Northern blot is 50% formalin with 1 mg of heparin at 42� C., with the hybridization being carried out overnight. An example of stringent wash conditions is a 0.2�SSC wash at 65� C. for 15 minutes (see, Sambrook et al., Molecular Cloning, A Laboratory Manual (3rd ed. 2001) for a description of SSC buffer). Often the high stringency wash is preceded by a low stringency wash to remove background probe signal. An example low stringency wash is 2�SSC at 40� C. for 15 minutes. In general, a signal to noise ratio of 5� (or higher) than that observed for an unrelated probe in the particular hybridization assay indicates detection of a specific hybridization. �Stringent hybridization wash conditions� in the context of nucleic acid hybridization experiments such as Southern and Northern hybridizations are sequence dependent, and are different under different environmental parameters. Longer sequences hybridize specifically at higher temperatures. An extensive guide to the hybridization of nucleic acids is found in Tijssen (1993), supra. and in Hames and Higgins, 1 and 2, supra. Stringent hybridization and wash conditions can easily be determined empirically for any test nucleic acid. For example, in determining highly stringent hybridization and wash conditions, the hybridization and wash conditions are gradually increased (e.g., by increasing temperature, decreasing salt concentration, increasing detergent concentration and/or increasing the concentration of organic solvents such as formalin in the hybridization or wash), until a selected set of criteria are met. For example, the hybridization and wash conditions are gradually increased until a probe binds to a perfectly matched complementary target with a signal to noise ratio that is at least 5� as high as that observed for hybridization of the probe to an unmatched target. �Very stringent� conditions are selected to be equal to the thermal melting point (Tm) for a particular probe. The Tm is the temperature (under defined ionic strength and pH) at which 50% of the test sequence hybridizes to a perfectly matched probe. For the purposes of the present invention, generally, �highly stringent� hybridization and wash conditions are selected to be about 5� C. lower than the Tm for the specific sequence at a defined ionic strength and pH. �Ultra high-stringency� hybridization and wash conditions are those in which the stringency of hybridization and wash conditions are increased until the signal to noise ratio for binding of the probe to the perfectly matched complementary target nucleic acid is at least 10� as high as that observed for hybridization to any of the unmatched target nucleic acids. A target nucleic acid which hybridizes to a probe under such conditions, with a signal to noise ratio of at least � that of the perfectly matched complementary target nucleic acid is said to bind to the probe under ultra-high stringency conditions. Similarly, even higher levels of stringency can be determined by gradually increasing the hybridization and/or wash conditions of the relevant hybridization assay. For example, those in which the stringency of hybridization and wash conditions are increased until the signal to noise ratio for binding of the probe to the perfectly matched complementary target nucleic acid is at least 10�, 20�, 50�, 100�, or 500� or more as high as that observed for hybridization to any of the unmatched target nucleic acids. A target nucleic acid which hybridizes to a probe under such conditions, with a signal to noise ratio of at least � that of the perfectly matched complementary target nucleic acid is said to bind to the probe under ultra-ultra-high stringency conditions. Nucleic acids which do not hybridize to each other under stringent conditions are still substantially identical if the polypeptides which they encode are substantially identical. This occurs, e.g., when a copy of a nucleic acid is created using the maximum codon degeneracy permitted by the genetic code. Unique Subsequences In one aspect, the invention provides a nucleic acid that comprises a unique subsequence in a nucleic acid selected from the sequences of O-tRNA's and O-RSs disclosed herein. The unique subsequence is unique as compared to a nucleic acid corresponding to any known O-tRNA or O-RS nucleic acid sequence. Alignment can be performed using, e.g., BLAST set to default parameters. Any unique subsequence is useful, e.g., as a probe to identify the nucleic acids of the present invention. Similarly, the invention includes a polypeptide which comprises a unique subsequence in a polypeptide selected from the sequences of O-RSs disclosed herein. Here, the unique subsequence is unique as compared to a polypeptide corresponding to any of known polypeptide sequence. The invention also provides for target nucleic acids which hybridizes under stringent conditions to a unique coding oligonucleotide which encodes a unique subsequence in a polypeptide selected from the sequences of O-RSs wherein the unique subsequence is unique as compared to a polypeptide corresponding to any of the control polypeptides (e.g., parental sequences from which synthetases of the present invention were derived, e.g., by mutation). Unique sequences are determined as noted above. Sequence Comparison, Identity, and Homology The terms �identical� or percent �identity,� in the context of two or more nucleic acid or polypeptide sequences, refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues or nucleotides that are the same, when compared and aligned for maximum correspondence over a comparison window, or designated region, as measured using one of the sequence comparison algorithms described below (or other algorithms available to persons of ordinary skill in the art) or by manual alignment and visual inspection. The phrase �substantially identical,� in the context of two nucleic acids or polypeptides (e.g., DNAs encoding an O-tRNA or O-RS, or the amino acid sequence of an O-RS) refers to two or more sequences or subsequences that have at least about 60%, about 80%, about 90-95%, about 98%, about 99% or more nucleotide or amino acid residue identity, when compared and aligned for maximum correspondence over a comparison window, or designated region, as measured using a sequence comparison algorithm (or other algorithms available to persons of ordinary skill in the art) or by manual alignment and visual inspection. Such �substantially identical� sequences are typically considered to be �homologous,� without reference to actual ancestry. �Substantial identity� may exist over a region of the sequences that is at least about 50 residues in length, a region of at least about 100 residues, or a region of at least about 150 residues, or over the full length of the two sequences to be compared. For sequence comparison and homology determination, typically one sequence acts as a reference sequence to which test sequences are compared. When using a sequence comparison algorithm, test and reference sequences are input into a computer, subsequence coordinates are designated, if necessary, and sequence algorithm program parameters are designated. The sequence comparison algorithm then calculates the percent sequence identity for the test sequence(s) relative to the reference sequence, based on the designated program parameters. Methods of alignment of sequences for comparison are known to those of ordinary skill in the art. Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482c (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see e.g., Ausubel et al., Current Protocols in Molecular Biology (1995 supplement)). One example of an algorithm that is suitable for determining percent sequence identity and sequence similarity is the BLAST algorithm and BLAST 2.0 algorithms, which are described in Altschul et al. (1997) Nuc. Acids Res. 25:3389-3402, and Altschul et al., J. Mol. Biol. 215:403-410 (1990). Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information available at the World Wide Web at ncbi.nlm.nih.gov. This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word of the same length in a database sequence. T is referred to as the neighborhood word score threshold (Altschul et al., supra). These initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them. The word hits are then extended in both directions along each sequence for as far as the cumulative alignment score can be increased. Cumulative scores are calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always>0) and N (penalty score for mismatching residues; always<0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the alignment. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, an expectation (E) of 10, a cutoff of 100, M=5, N=−4, and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength (W) of 3, an expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff & Henikoff (1992) Proc. Natl. Acad. Sci. USA 89:10915) alignments (B) of 50, expectation (E) of 10, M=5, N=−4, and a comparison of both strands. The BLAST algorithm is typically performed with the �low complexity� filter turned off. In addition to calculating percent sequence identity, the BLAST algorithm also performs a statistical analysis of the similarity between two sequences (see, e.g., Karlin & Altschul, Proc. Nat'l. Acad. Sci. USA 90:5873-5787 (1993)). One measure of similarity provided by the BLAST algorithm is the smallest sum probability (P(N)), which provides an indication of the probability by which a match between two nucleotide or amino acid sequences would occur by chance. For example, a nucleic acid may be considered similar to a reference sequence if the smallest sum probability in a comparison of the test nucleic acid to the reference nucleic acid is less than about 0.2, less than about 0.01, or less than about 0.001. Mutagenesis and Other Molecular Biology Techniques Polynucleotide and polypeptides of the present invention and used in the invention can be manipulated using molecular biological techniques. A nucleotide sequence may be conveniently modified by site-directed mutagenesis in accordance with conventional methods. Alternatively, the nucleotide sequence may be prepared by chemical synthesis, including but not limited to, by using an oligonucleotide synthesizer, wherein oligonucleotides are designed based on the amino acid sequence of the desired polypeptide, and preferably selecting those codons that are favored in the host cell in which the recombinant polypeptide will be produced. For example, several small oligonucleotides coding for portions of the desired polypeptide may be synthesized and assembled by PCR, ligation or ligation chain reaction. See, e.g., Barany, et al., Proc. Natl. Acad. Sci. 88: 189-193 (1991); U.S. Pat. No. 6,521,427 which are incorporated by reference herein. This invention utilizes routine techniques in the field of recombinant genetics. Basic texts disclosing the general methods of use in this invention include Sambrook et al., Molecular Cloning, A Laboratory Manual (3rd ed. 2001); Kriegler, Gene Transfer and Expression: A Laboratory Manual (1990); and Current Protocols in Molecular Biology (Ausubel et al., eds., 1994)). General texts which describe molecular biological techniques include Berger and Kimmel, Guide to Molecular Cloning Techniques, Methods in Enzymology volume 152 Academic Press, Inc., San Diego, Calif. (Berger); Sambrook et al., Molecular Cloning�A Laboratory Manual (2nd Ed.). Vol. 1-3, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., 1989 (�Sambrook�) and Current Protocols in Molecular Biology, F. M. Ausubel et al., eds., Current Protocols, a joint venture between Greene Publishing Associates, Inc. and John Wiley & Sons, Inc., (supplemented through 1999) (�Ausubel�)). These texts describe mutagenesis, the use of vectors, promoters and many other relevant topics related to, e.g., the generation of genes or polynucleotides that include selector codons for production of proteins that include selected amino acids (e.g., unnatural amino acids), orthogonal tRNA's, orthogonal synthetases, and pairs thereof. Various types of mutagenesis are used in the invention for a variety of purposes, including but not limited to, to produce novel synthetases or tRNAs, to mutate tRNA molecules, to produce libraries of tRNAs, to mutate RS molecules, to produce libraries of synthetases, to produce selector codons, to insert selector codons that encode a selected amino acid in a protein or polypeptide of interest. They include but are not limited to, site-directed, random point mutagenesis, homologous recombination, DNA shuffling or other recursive mutagenesis methods, chimeric construction, mutagenesis using uracil containing templates, oligonucleotide-directed mutagenesis, phosphorothioate-modified DNA mutagenesis, mutagenesis using gapped duplex DNA or the like, or any combination thereof. Additional suitable methods include point mismatch repair, mutagenesis using repair-deficient host strains, restriction-selection and restriction-purification, deletion mutagenesis, mutagenesis by total gene synthesis, double-strand break repair, and the like. Mutagenesis, including but not limited to, involving chimeric constructs, is also included in the present invention. In one embodiment, mutagenesis can be guided by known information of the naturally occurring molecule or altered or mutated naturally occurring molecule, including but not limited to, sequence, sequence comparisons, physical properties, secondary, tertiary, or quaternary structure, crystal structure or the like. The texts and examples found herein describe these procedures. Additional information is found in the following publications and references cited within: Ling et al., Approaches to DNA mutagenesis: an overview, Anal Biochem. 254(2): 157-178 (1997); Dale et al., Oligonucleotide-directed random mutagenesis using the phosphorothioate method, Methods Mol. Biol. 57:369-374 (1996); Smith, In vitro mutagenesis, Ann. Rev. Genet. 19:423-462 (1985); Botstein & Shortle, Strategies and applications of in vitro mutagenesis, Science 229:1193-1201 (1985); Carter, Site-directed mutagenesis, Biochem. J. 237:1-7 (1986); Kunkel, The efficiency of oligonucleotide directed mutagenesis, in Nucleic Acids & Molecular Biology (Eckstein, F. and Lilley, D. M. J. eds., Springer Verlag, Berlin) (1987); Kunkel, Rapid and efficient site-specific mutagenesis without phenotypic selection, Proc. Natl. Acad. Sci. USA 82:488-492 (1985); Kunkel et al., Rapid and efficient site-specific mutagenesis without phenotypic selection, Methods in Enzymol. 154, 367-382 (1987); Bass et al., Mutant Trp repressors with new DNA-binding specificities, Science 242:240-245 (1988); Zoller & Smith, Oligonucleotide-directed mutagenesis using M13-derived vectors: an efficient and general procedure for the production of point mutations in any DNA fragment, Nucleic Acids Res. 10:6487-6500 (1982); Zoller & Smith, Oligonucleotide-directed mutagenesis of DNA fragments cloned into M13 vectors, Methods in Enzymol. 100:468-500 (1983); Zoller & Smith, Oligonucleotide-directed mutagenesis: a simple method using two oligonucleotide primers and a single-stranded DNA template, Methods in Enzymol. 154:329-350 (1987); Taylor et al., The use of phosphorothioate-modified DNA in restriction enzyme reactions to prepare nicked DNA, Nucl. Acids Res. 13: 8749-8764 (1985); Taylor et al., The rapid generation of oligonucleotide-directed mutations at high frequency using phosphorothioate-modified DNA, Nucl. Acids Res. 13: 8765-8785 (1985); Nakamaye & Eckstein, Inhibition of restriction endonuclease Nci I cleavage by phosphorothioate groups and its application to oligonucleotide-directed mutagenesis, Nucl. Acids Res. 14: 9679-9698 (1986); Sayers et al., 5′-3′ Exonucleases in phosphorothioate-based oligonucleotide-directed mutagenesis, Nucl. Acids Res. 16:791-802 (1988); Sayers et al., Strand specific cleavage of phosphorothioate-containing DNA by reaction with restriction endonucleases in the presence of ethidium bromide, (1988) Nucl. Acids Res. 16: 803-814; Kramer et al., The gapped duplex DNA approach to oligonucleotide-directed mutation construction, Nucl. Acids Res. 12: 9441-9456 (1984); Kramer & Fritz Oligonucleotide-directed construction of mutations via gapped duplex DNA, Methods in Enzymol. 154:350-367 (1987); Kramer et al., Improved enzymatic in vitro reactions in the gapped duplex DNA approach to oligonucleotide-directed construction of mutations, Nucl. Acids Res. 16: 7207 (1988); Fritz et al., Oligonucleotide-directed construction of mutations: a gapped duplex DNA procedure without enzymatic reactions in vitro, Nucl. Acids Res. 16: 6987-6999 (1988); Kramer et al., Different base/base mismatches are corrected with different efficiencies by the methyl-directed DNA mismatch-repair system of E. coli, Cell 38:879-887 (1984); Carter et al., Improved oligonucleotide site-directed mutagenesis using M13 vectors, Nucl. Acids Res. 13: 4431-4443 (1985); Carter, Improved oligonucleotide-directed mutagenesis using M13 vectors, Methods in Enzymol. 154:382-403 (1987); Eghtedarzadeh & Henikoff, Use of oligonucleotides to generate large deletions, Nucl. Acids Res. 14:5115 (1986); Wells et al., Importance of hydrogen-bond formation in stabilizing the transition state of subtilisin, Phil. Trans. R. Soc. Lond. A 317: 415-423 (1986); Nambiar et al., Total synthesis and cloning of a gene coding for the ribonuclease S protein, Science 223:1299-1301 (1984); Sakmar and Khorana, Total synthesis and expression of a gene for the alpha-subunit of bovine rod outer segment guanine nucleotide-binding protein (transducin), Nucl. Acids Res. 14:6361-6372 (1988); Wells et al., Cassette mutagenesis: an efficient method for generation of multiple mutations at defined sites, Gene 34:315-323 (1985); Grundstr�m et al., Oligonucleotide-directed mutagenesis by microscale �shot-gun� gene synthesis, Nucl. Acids Res. 13: 3305-3316 (1985); Mandecki, Oligonucleotide-directed double-strand break repair in plasmids of Escherichia coli: a method for site-specific mutagenesis, Proc. Natl. Acad. Sci. USA, 83:7177-7181 (1986); Arnold, Protein engineering for unusual environments, Current Opinion in Biotechnology 4:450-455 (1993); Sieber, et al., Nature Biotechnology, 19:456-460 (2001); W. P. C. Stemmer, Nature 370, 389-91 (1994); and, I. A. Lorimer, I. Pastan, Nucleic Acids Res. 23, 3067-8 (1995). Additional details on many of the above methods can be found in Methods in Enzymology Volume 154, which also describes useful controls for trouble-shooting problems with various mutagenesis methods. Oligonucleotides, e.g., for use in mutagenesis of the present invention, e.g., mutating libraries of synthetases, or altering tRNAs, are typically synthesized chemically according to the solid phase phosphoramidite triester method described by Beaucage and Caruthers, Tetrahedron Letts. 22(20):1859-1862, (1981) e.g., using an automated synthesizer, as described in Needham-VanDevanter et al., Nucleic Acids Res., 12:6159-6168 (1984). In addition, essentially any nucleic acid can be custom or standard ordered from any of a variety of commercial sources, such as The Midland Certified Reagent Company (mcrc@oligos.com), The Great American Gene Company (www.genco.com), ExpressGen Inc. (www.expressgen.com), Operon Technologies Inc. (Alameda, Calif.) and many others. The invention also relates to eukaryotic host cells, non-eukaryotic host cells, and organisms for the in vivo incorporation of an unnatural amino acid via orthogonal tRNA/RS pairs. Host cells are genetically engineered (including but not limited to, transformed, transduced or transfected) with the polynucleotides of the present invention or constructs which include a polynucleotide of the present invention, including but not limited to, a vector of the present invention, which can be, for example, a cloning vector or an expression vector. For example, the coding regions for the orthogonal tRNA, the orthogonal tRNA synthetase, and the protein to be derivatized are operably linked to gene expression control elements that are functional in the desired host cell. The vector can be, for example, in the form of a plasmid, a cosmid, a phage, a bacterium, a virus, a naked polynucleotide, or a conjugated polynucleotide. The vectors are introduced into cells and/or microorganisms by standard methods including electroporation (Fromm et al., Proc. Natl. Acad. Sci. USA 82, 5824 (1985)), infection by viral vectors, high velocity ballistic penetration by small particles with the nucleic acid either within the matrix of small beads or particles, or on the surface (Klein et al., Nature 327, 70-73 (1987)), and/or the like. Several well-known methods of introducing target nucleic acids into cells are available, any of which can be used in the invention. These include: fusion of the recipient cells with bacterial protoplasts containing the DNA, electroporation, projectile bombardment, and infection with viral vectors (discussed further, below), etc. Bacterial cells can be used to amplify the number of plasmids containing DNA constructs of this invention. The bacteria are grown to log phase and the plasmids within the bacteria can be isolated by a variety of methods known in the art (see, for instance, Sambrook). In addition, kits are commercially available for the purification of plasmids from bacteria, (see, e.g., EasyPrep�, FlexiPrep�, both from Pharmacia Biotech; StrataClean� from Stratagene; and, QIAprep� from Qiagen). The isolated and purified plasmids are then further manipulated to produce other plasmids, used to transfect cells or incorporated into related vectors to infect organisms. Typical vectors contain transcription and translation terminators, transcription and translation initiation sequences, and promoters useful for regulation of the expression of the particular target nucleic acid. The vectors optionally comprise generic expression cassettes containing at least one independent terminator sequence, sequences permitting replication of the cassette in eukaryotes, or prokaryotes, or both, (including but not limited to, shuttle vectors) and selection markers for both prokaryotic and eukaryotic systems. Vectors are suitable for replication and/or integration in prokaryotes, eukaryotes, or both. See, Gillam & Smith, Gene 8:81 (1979); Roberts, et al., Nature, 328:731 (1987); Schneider, E., et al., Protein Expr. Purif. 6(1)10-14 (1995); Ausubel, Sambrook, Berger (all supra). A catalogue of bacteria and bacteriophages useful for cloning is provided, e.g., by the ATCC, e.g., The ATCC Catalogue of Bacteria and Bacteriophage (1992) Gherna et al. (eds) published by the ATCC. Additional basic procedures for sequencing, cloning and other aspects of molecular biology and underlying theoretical considerations are also found in Watson et al. (1992) Recombinant DNA Second Edition Scientific American Books, NY. In addition, essentially any nucleic acid (and virtually any labeled nucleic acid, whether standard or non-standard) can be custom or standard ordered from any of a variety of commercial sources, such as the Midland Certified Reagent Company (Midland, Tex. available on the World Wide Web at mcrc.com), The Great American Gene Company (Ramona, Calif. available on the World Wide Web at genco.com), ExpressGen Inc. (Chicago, Ill. available on the World Wide Web at expressgen.com), Operon Technologies Inc. (Alameda, Calif.) and many others. The engineered host cells can be cultured in conventional nutrient media modified as appropriate for such activities as, for example, screening steps, activating promoters or selecting transformants. These cells can optionally be cultured into transgenic organisms. Other useful references, e.g. for cell isolation and culture (e.g., for subsequent nucleic acid isolation) include Freshney (1994) Culture of Animal Cells, a Manual of Basic Technique, third edition, Wiley-Liss, New York and the references cited therein; Payne et al. (1992) Plant Cell and Tissue Culture in Liquid Systems John Wiley & Sons, Inc. New York, N.Y.; Gamborg and Phillips (eds.) (1995) Plant Cell, Tissue and Organ Culture; Fundamental Methods Springer Lab Manual, Springer-Verlag (Berlin Heidelberg New York) and Atlas and Parks (eds.) The Handbook of Microbiological Media (1993) CRC Press, Boca Raton, Fla. The ability to incorporate unnatural amino acids directly into proteins in vivo offers a wide variety of advantages including but not limited to high yields of mutant proteins, technical ease, the potential to study the mutant proteins in cells or possibly in living organisms and the use of these mutant proteins in therapeutic treatments and diagnostic uses. The ability to include unnatural amino acids with various sizes, acidities, nucleophilicities, hydrophobicities, and other properties into proteins can greatly expand our ability to rationally and systematically manipulate the structures of proteins, both to probe protein function and create new proteins or organisms with novel properties. Proteins and Polypeptides of Interest The incorporation of an unnatural amino acid can be done for a variety of purposes, including but not limited to, tailoring changes in protein structure and/or function, changing size, acidity, nucleophilicity, hydrogen bonding, hydrophobicity, accessibility of protease target sites, targeting to a moiety (including but not limited to, for a protein array), adding a biologically active molecule, attaching a polymer, attaching a radionuclide, modulating serum half-life, modulating tissue penetration (e.g. tumors), modulating active transport, modulating tissue, cell or organ specificity or distribution, modulating immunogenicity, modulating protease resistance, etc. Proteins that include an unnatural amino acid can have enhanced or even entirely new catalytic or biophysical properties. For example, the following properties are optionally modified by inclusion of an unnatural amino acid into a protein: toxicity, biodistribution, structural properties, spectroscopic properties, chemical and/or photochemical properties, catalytic ability, half-life (including but not limited to, serum half-life), ability to react with other molecules, including but not limited to, covalently or noncovalently, and the like. The compositions including proteins that include at least one unnatural amino acid are useful for, including but not limited to, novel therapeutics, diagnostics, catalytic enzymes, industrial enzymes, binding proteins (including but not limited to, antibodies), and including but not limited to, the study of protein structure and function. See, e.g., Dougherty, (2000) Unnatural Amino Acids as Probes of Protein Structure and Function, Current Opinion in Chemical Biology, 4:645-652. A protein may have at least one, including but not limited to, at least two, at least three, at least four, at least five, at least six, at least seven, at least eight, at least nine, or at least ten or more unnatural amino acids. The unnatural amino acids can be the same or different, including but not limited to, there can be 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more different sites in the protein that comprise 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 or more different unnatural amino acids. A protein may have at least one, but fewer than all, of a particular amino acid present in the protein is substituted with the unnatural amino acid. For a given protein with more than one unnatural amino acids, the unnatural amino acids can be identical or different (including but not limited to, the protein can include two or more different types of unnatural amino acids, or can include two of the same unnatural amino acid). For a given protein with more than two unnatural amino acids, the unnatural amino acids can be the same, different or a combination of a multiple unnatural amino acid of the same kind with at least one different unnatural amino acid. By producing proteins or polypeptides of interest with at least one unnatural amino acid in eukaryotic cells, proteins or polypeptides will typically include eukaryotic post-translational modifications. In certain embodiments, a protein includes at least one unnatural amino acid and at least one post-translational modification that is made in vivo by a eukaryotic cell, where the post-translational modification is not made by a prokaryotic cell. For example, the post-translation modification includes, including but not limited to, acetylation, acylation, lipid-modification, palmitoylation, palmitate addition, phosphorylation, glycolipid-linkage modification, glycosylation, and the like. In yet another aspect, the post-translation modification includes proteolytic processing of precursors (including but not limited to, calcitonin precursor, calcitonin gene-related peptide precursor, preproparathyroid hormone, preproinsulin, proinsulin, prepro-opiomelanocortin, pro-opiomelanocortin and the like), assembly into a multisubunit protein or macromolecular assembly, translation to another site in the cell (including but not limited to, to organelles, such as the endoplasmic reticulum, the Golgi apparatus, the nucleus, lysosomes, peroxisomes, mitochondria, chloroplasts, vacuoles, etc., or through the secretory pathway). In certain embodiments, the protein comprises a secretion or localization sequence, an epitope tag, a FLAG tag, a polyhistidine tag, a GST fusion, or the like. Methods of producing a protein in a cell with a selected amino acid at a specified position are also a feature of the present invention. For example, a method includes growing, in an appropriate medium, the cell, where the cell comprises a nucleic acid that comprises at least one selector codon and encodes a protein; and, providing the selected amino acid; where the cell further comprises: an orthogonal tRNA (O-tRNA) that functions in the cell and recognizes the selector codon; and, an orthogonal aminoacyl-tRNA synthetase (O-RS) that preferentially aminoacylates the O-tRNA with the selected amino acid. Typically, the O-tRNA comprises suppression activity in presence of a cognate synthetase in response to a selector codon. A protein produced by this method is also a feature of the present invention. The compositions of the present invention and compositions made by the methods of the present invention optionally are in a cell. The O-tRNA/O-RS pairs or individual components of the present invention can then be used in a host system's translation machinery, which results in a selected amino acid, e.g., unnatural amino acid, being incorporated into a protein. Patent applications U.S. Ser. Nos. 10/825,867, entitled �Expanding the Eukaryotic Genetic Code;� and 10/126,927, entitled �IN VIVO INCORPORATION OF UNNATURAL AMINO ACIDS�, describe this process and are incorporated herein by reference. For example, when an O-tRNA/O-RS pair is introduced into a host, e.g., Escherichia coli, the pair leads to the in vivo incorporation of selected amino acid, such as an unnatural amino acid, e.g., a synthetic amino acid, such as derivative of a leucine amino acid, which can be exogenously added to the growth medium, into a protein, in response to a selector codon. Optionally, the compositions of the present invention can be in an in vitro translation system, or in an in vivo system(s). Any protein (or portion thereof) that includes a selected amino acid, e.g., an unnatural amino acid, (and any corresponding coding nucleic acid, e.g., which includes one or more selector codons) can be produced using the compositions and methods herein. Any polypeptide is suitable for incorporation of one or more selected amino acids. No attempt is made to identify the hundreds of thousands of known proteins, any of which can be modified to include one or more unnatural amino acid, e.g., by tailoring any available mutation methods to include one or more appropriate selector codon in a relevant translation system. Common sequence repositories for known proteins include GenBank EMBL, DDBJ and the NCBI. Other repositories can easily be identified by searching the internet. Typically, the proteins are, e.g., at least 60%, at least 70%, at least 75%, at least 80%, at least 90%, at least 95%, or at least 99% or more identical to any available protein (e.g., a therapeutic protein, a diagnostic protein, an industrial enzyme, or portion thereof, and the like), and they comprise one or more selected amino acid. Examples of therapeutic, diagnostic, and other proteins that can be modified to comprise one or more selected amino acid, e.g., an unnatural amino acid, can be found, but not limited to, those in U.S. Ser. No. 10/825,867 entitled �Expanding the Eukaryotic Genetic Code;� and, U.S. patent application Ser. No. 10/126,927, entitled �IN VIVO INCORPORATION OF UNNATURAL AMINO ACIDS.� In certain embodiments, the protein or polypeptide of interest (or portion thereof) in the methods and/or compositions of the present invention is encoded by a nucleic acid. Typically, the nucleic acid comprises at least one selector codon, at least two selector codons, at least three selector codons, at least four selector codons, at least five selector codons, at least six selector codons, at least seven selector codons, at least eight selector codons, at least nine selector codons, ten or more selector codons. Genes coding for proteins or polypeptides of interest can be mutagenized using methods well-known to one of skill in the art and described herein under �Mutagenesis and Other Molecular Biology Techniques� to include, e.g., one or more selector codon for the incorporation of a selected amino acid, e.g., an unnatural amino acid. For example, a nucleic acid for a protein of interest is mutagenized to include one or more selector codon, providing for the insertion of the one or more selected amino acids, e.g., unnatural amino acid. The invention includes any such variant, e.g., mutant, versions of any protein, e.g., including at least one selected amino acid. Similarly, the invention also includes corresponding nucleic acids, i.e., any nucleic acid with one or more selector codon that encodes one or more selected amino acid. To make a protein that includes a selected amino acid, one can use host cells and organisms that are adapted for the in vivo incorporation of the selected amino acid via orthogonal tRNA/RS pairs. Host cells are genetically engineered (e.g., transformed, transduced or transfected) with one or more vectors that express the orthogonal tRNA, the orthogonal tRNA synthetase, and a vector that encodes the protein to be derivatized. Each of these components can be on the same vector, or each can be on a separate vector, two components can be on one vector and the third component on a second vector. The vector can be, for example, in the form of a plasmid, a cosmid, a phage, a bacterium, a virus, a naked polynucleotide, or a conjugated polynucleotide. Alternate Systems Several strategies have been employed to introduce unnatural amino acids into proteins in non-recombinant host cells, mutagenized host cells, or in cell-free systems. Derivatization of amino acids with reactive side-chains such as Lys, Cys and Tyr resulted in the conversion of lysine to N2-acetyl-lysine. Chemical synthesis also provides a straightforward method to incorporate unnatural amino acids. With the recent development of enzymatic ligation and native chemical ligation of peptide fragments, it is possible to make larger proteins. See, e.g., P. E. Dawson and S. B. H. Kent, Annu. Rev. Biochem, 69:923 (2000). Chemical peptide ligation and native chemical ligation are described in U.S. Pat. No. 6,184,344, U.S. Patent Publication No. 2004/0138412, U.S. Patent Publication No. 2003/0208046, WO 02/098902, and WO 03/042235, which are incorporated by reference herein. A general in vitro biosynthetic method in which a suppressor tRNA chemically acylated with the desired unnatural amino acid is added to an in vitro extract capable of supporting protein biosynthesis, has been used to site-specifically incorporate over 100 unnatural amino acids into a variety of proteins of virtually any size. See, e.g., V. W. Cornish, D. Mendel and P. G. Schultz, Angew. Chem. Int. Ed. Engl., 1995, 34:621 (1995); C. J. Noren, S. J. Anthony-Cahill, M. C. Griffith, P. G. Schultz, A general method for site-specific incorporation of unnatural amino acids into proteins, Science 244:182-188 (1989); and, J. D. Bain, C. G. Glabe, T. A. Dix, A. R. Chamberlin, E. S. Diala, Biosynthetic site-specific incorporation of a non-natural amino acid into a polypeptide, J. Am. Chem. Soc. 111:8013-8014 (1989). A broad range of functional groups has been introduced into proteins for studies of protein stability, protein folding, enzyme mechanism, and signal transduction. An in vivo method, termed selective pressure incorporation, was developed to exploit the promiscuity of wild-type synthetases. See, e.g., N. Budisa, C. Minks, S. Alefelder, W. Wenger, F. M. Dong, L. Moroder and R. Huber, FASEB J., 13:41 (1999). An auxotrophic strain, in which the relevant metabolic pathway supplying the cell with a particular natural amino acid is switched off, is grown in minimal media containing limited concentrations of the natural amino acid, while transcription of the target gene is repressed. At the onset of a stationary growth phase, the natural amino acid is depleted and replaced with the unnatural amino acid analog. Induction of expression of the recombinant protein results in the accumulation of a protein containing the unnatural analog. For example, using this strategy, o, m and p-fluorophenylalanines have been incorporated into proteins, and exhibit two characteristic shoulders in the UV spectrum which can be easily identified, see, e.g., C. Minks, R. Huber, L. Moroder and N. Budisa, Anal. Biochem., 284:29 (2000); trifluoromethionine has been used to replace methionine in bacteriophage T4 lysozyme to study its interaction with chitooligosaccharide ligands by 19F NMR, see, e.g., H. Duewel, E. Daub, V. Robinson and J. F. Honek, Biochemistry, 36:3404 (1997); and trifluoroleucine has been incorporated in place of leucine, resulting in increased thermal and chemical stability of a leucine-zipper protein. See, e.g., Y. Tang, G. Ghirlanda, W. A. Petka, T. Nakajima, W. F. DeGrado and D. A. Tirrell, Angew. Chem. Int. Ed. Engl., 40:1494 (2001). Moreover, selenomethionine and telluromethionine are incorporated into various recombinant proteins to facilitate the solution of phases in X-ray crystallography. See, e.g., W. A. Hendrickson, J. R. Horton and D. M. Lemaster, EMBO J., 9:1665 (1990); J. O. Boles, K. Lewinski, M. Kunkle, J. D. Odom, B. Dunlap, L. Lebioda and M. Hatada, Nat. Struct. Biol., 1:283 (1994); N. Budisa, B. Steipe, P. Demange, C. Eckerskorn, J. Kellermann and R. Huber, Eur. J. Biochem., 230:788 (1995); and, N. Budisa, W. Karnbrock, S. Steinbacher, A. Humm, L. Prade, T. Neuefeind, L. Moroder and R. Huber, J. Mol. Biol. 270:616 (1997). Methionine analogs with alkene or alkyne functionalities have also been incorporated efficiently, allowing for additional modification of proteins by chemical means. See, e.g., J. C. van Hest and D. A. Tirrell, FEBS Lett., 428:68 (1998); J. C. van Hest, K. L. Kiick and D. A. Tirrell, J. Am. Chem. Soc., 122:1282 (2000); and, K. L. Kiick and D. A. Tirrell, Tetrahedron, 56:9487 (2000); U.S. Pat. No. 6,586,207; U.S. Patent Publication 2002/0042097, which are incorporated by reference herein. The success of this method depends on the recognition of the unnatural amino acid analogs by aminoacyl-tRNA synthetases, which, in general, require high selectivity to insure the fidelity of protein translation. One way to expand the scope of this method is to relax the substrate specificity of aminoacyl-tRNA synthetases, which has been achieved in a limited number of cases. For example, replacement of Ala294 by Gly in Escherichia coli phenylalanyl-tRNA synthetase (PheRS) increases the size of substrate binding pocket, and results in the acylation of tRNAPhe by p-Cl-phenylalanine (p-Cl-Phe). See, M. Ibba, P. Kast and H. Hennecke, Biochemistry, 33:7107 (1994). An Escherichia coli strain harboring this mutant PheRS allows the incorporation of p-Cl-phenylalanine or p-Br-phenylalanine in place of phenylalanine. See, e.g., M. Ibba and H. Hennecke, FEBS Lett., 364:272 (1995); and, N. Sharma, R. Furter, P. Kast and D. A. Tirrell, FEBS Lett., 467:37 (2000). Similarly, a point mutation Phe130Ser near the amino acid binding site of Escherichia coli tyrosyl-tRNA synthetase was shown to allow azatyrosine to be incorporated more efficiently than tyrosine. See, F. Hamano-Takaku, T. Iwama, S. Saito-Yano, K. Takaku, Y. Monden, M. Kitabatake, D. Soll and S. Nishimura, J. Biol. Chem., 275:40324 (2000). Another strategy to incorporate unnatural amino acids into proteins in vivo is to modify synthetases that have proofreading mechanisms. These synthetases cannot discriminate and therefore activate amino acids that are structurally similar to the cognate natural amino acids. This error is corrected at a separate site, which deacylates the mischarged amino acid from the tRNA to maintain the fidelity of protein translation. If the proofreading activity of the synthetase is disabled, structural analogs that are misactivated may escape the editing function and be incorporated. This approach has been demonstrated recently with the valyl-tRNA synthetase (VaIRS). See, V. Doring, H. D. Mootz, L. A. Nangle, T. L. Hendrickson, V. de Crecy-Lagard, P. Schimmel and P. Marliere, Science, 292:501 (2001). VaIRS can misaminoacylate tRNAVal with Cys, Thr, or aminobutyrate (Abu); these noncognate amino acids are subsequently hydrolyzed by the editing domain. After random mutagenesis of the Escherichia coli chromosome, a mutant Escherichia coli strain was selected that has a mutation in the editing site of VaIRS. This edit-defective VaIRS incorrectly charges tRNAVal with Cys. Because Abu sterically resembles Cys (�SH group of Cys is replaced with �CH3 in Abu), the mutant VaIRS also incorporates Abu into proteins when this mutant Escherichia coli strain is grown in the presence of Abu. Mass spectrometric analysis shows that about 24% of valines are replaced by Abu at each valine position in the native protein. Solid-phase synthesis and semisynthetic methods have also allowed for the synthesis of a number of proteins containing novel amino acids. For example, see the following publications and references cited within, which are as follows: Crick, F. H. C., Barrett, L. Brenner, S. Watts-Tobin, R. General nature of the genetic code for proteins. Nature, 192:1227-1232 (1961); Hofmann, K., Bohn, H. Studies on polypeptides. XXXVI. The effect of pyrazole-imidazole replacements on the S-protein activating potency of an S-peptide fragment, J. Am. Chem, 88(24):5914-5919 (1966); Kaiser, E. T. Synthetic approaches to biologically active peptides and proteins including enyzmes, Acc Chem Res, 22:47-54 (1989); Nakatsuka, T., Sasaki, T., Kaiser, E. T. Peptide segment coupling catalyzed by the semisynthetic enzyme thiosubtilisin, J Am Chem Soc, 109:3808-3810 (1987); Schnolzer, M., Kent, S B H. Constructing proteins by dovetailing unprotected synthetic peptides: backbone-engineered HIV protease, Science, 256(5054):221-225 (1992); Chaiken, I. M. Semisynthetic peptides and proteins, CRC Crit. Rev Biochem, 11(3):255-301 (1981); Offord, R. E. Protein engineering by chemical means? Protein Eng., 1(3):151-157 (1987); and, Jackson, D. Y., Burnier, J., Quan, C., Stanley, M., Tom, J., Wells, J. A. A Designed Peptide Ligase for Total Synthesis of Ribonuclease A with Unnatural Catalytic Residues, Science, 266(5183):243 (1994). Chemical modification has been used to introduce a variety of unnatural side chains, including cofactors, spin labels and oligonucleotides into proteins in vitro. See, e.g., Corey, D. R., Schultz, P. G. Generation of a hybrid sequence-specific single-stranded deoxyribonuclease, Science, 238(4832):1401-1403 (1987); Kaiser, E. T., Lawrence D. S., Rokita, S. E. The chemical modification of enzymatic specificity, Annu Rev Biochem, 54:565-595 (1985); Kaiser, E. T., Lawrence, D. S. Chemical mutation of enzyme active sites, Science, 226(4674):505-511 (1984); Neet, K. E., Nanci A, Koshland, D. E. Properties of thiol-subtilisin, J. Biol. Chem., 243(24):6392-6401 (1968); Polgar, L. et M. L. Bender. A new enzyme containing a synthetically formed active site. Thiol-subtilisin. J. Am. Chem Soc, 88:3153-3154 (1966); and, Pollack, S. J., Nakayama, G. Schultz, P. G. Introduction of nucleophiles and spectroscopic probes into antibody combining sites, Science, 242(4881):1038-1040 (1988). Defining Polypeptides by Immunoreactivity Because the polypeptides of the present invention provide a variety of new polypeptide sequences (e.g., comprising selected amino acids (e.g., unnatural amino acids) in the case of proteins synthesized in the translation systems herein, or, e.g., in the case of the novel synthetases, novel sequences of standard amino acids), the polypeptides also provide new structural features which can be recognized, e.g., in immunological assays. The generation of antisera, which specifically bind the polypeptides of the present invention, as well as the polypeptides which are bound by such antisera, are a feature of the present invention. The term �antibody,� as used herein, includes, but is not limited to a polypeptide substantially encoded by an immunoglobulin gene or immunoglobulin genes, or fragments thereof which specifically bind and recognize an analyte (antigen). Examples include polyclonal, monoclonal, chimeric, and single chain antibodies, and the like. Fragments of immunoglobulins, including Fab fragments and fragments produced by an expression library, including phage display, are also included in the term �antibody� as used herein. See, e.g., Paul, Fundamental Immunology, 4th Ed., 1999, Raven Press, New York, for antibody structure and terminology. For example, the invention includes proteins made utilizing the tRNAs and/or RSs of the present invention that specifically bind to or that are specifically immunoreactive with an antibody or antisera generated against an immunogen comprising an amino acid sequence. To eliminate cross-reactivity with other homologues, the antibody or antisera is subtracted with available protein, such as the wild-type polypeptide, e.g., the �control� polypeptides. Where the wild-type protein corresponds to a nucleic acid, a polypeptide encoded by the nucleic acid is generated and used for antibody/antisera subtraction purposes. In one typical format, the immunoassay uses a polyclonal antiserum which was raised against one or more polypeptide or a substantial subsequence thereof (i.e., at least about 30% of the full length sequence provided). The set of potential polypeptide immunogens derived from the protein are collectively referred to below as �the immunogenic polypeptides.� The resulting antisera is optionally selected to have low cross-reactivity against the control synthetase homologues and any such cross-reactivity is removed, e.g., by immunoabsorbtion, with one or more of the control homologues, prior to use of the polyclonal antiserum in the immunoassay. In order to produce antisera for use in an immunoassay, one or more of the immunogenic polypeptides is produced and purified as described herein. For example, recombinant protein can be produced in a recombinant cell. An inbred strain of mice (used in this assay because results are more reproducible due to the virtual genetic identity of the mice) is immunized with the immunogenic protein(s) in combination with a standard adjuvant, such as Freund's adjuvant, and a standard mouse immunization protocol (see, e.g., Harlow and Lane (1988) Antibodies, A Laboratory Manual, Cold Spring Harbor Publications, New York, for a standard description of antibody generation, immunoassay formats and conditions that can be used to determine specific immunoreactivity. Additional references and discussion of antibodies is also found herein and can be applied here to defining polypeptides by immunoreactivity). Alternatively, one or more synthetic or recombinant polypeptide derived from the sequences disclosed herein is conjugated to a carrier protein and used as an immunogen. Polyclonal sera are collected and titered against the immunogenic polypeptide in an immunoassay, for example, a solid phase immunoassay with one or more of the immunogenic proteins immobilized on a solid support. Polyclonal antisera with a titer of 106 or greater are selected, pooled and subtracted with the control synthetase polypeptides to produce subtracted pooled titered polyclonal antisera. The subtracted pooled titered polyclonal antisera are tested for cross reactivity against the control homologues in a comparative immunoassay. In this comparative assay, discriminatory binding conditions are determined for the subtracted titered polyclonal antisera which result in at least about a 5-10 fold higher signal to noise ratio for binding of the titered polyclonal antisera to the immunogenic protein as compared to binding to the control synthetase homologues. That is, the stringency of the binding reaction is adjusted by the addition of non-specific competitors such as albumin or non-fat dry milk, and/or by adjusting salt conditions, temperature, and/or the like. These binding conditions are used in subsequent assays for determining whether a test polypeptide (a polypeptide being compared to the immunogenic polypeptides and/or the control polypeptides) is specifically bound by the pooled subtracted polyclonal antisera. In another example, immunoassays in the competitive binding format are used for detection of a test polypeptide. For example, as noted, cross-reacting antibodies are removed from the pooled antisera mixture by immunoabsorbtion with the control polypeptides. The immunogenic polypeptide(s) are then immobilized to a solid support which is exposed to the subtracted pooled antisera. Test proteins are added to the assay to compete for binding to the pooled subtracted antisera. The ability of the test protein(s) to compete for binding to the pooled subtracted antisera as compared to the immobilized protein(s) is compared to the ability of the immunogenic polypeptide(s) added to the assay to compete for binding (the immunogenic polypeptides compete effectively with the immobilized immunogenic polypeptides for binding to the pooled antisera). The percent cross-reactivity for the test proteins is calculated, using standard calculations. In a parallel assay, the ability of the control proteins to compete for binding to the pooled subtracted antisera is optionally determined as compared to the ability of the immunogenic polypeptide(s) to compete for binding to the antisera. Again, the percent cross-reactivity for the control polypeptides is calculated, using standard calculations. Where the percent cross-reactivity is at least 5-10� as high for the test polypeptides as compared to the control polypeptides and or where the binding of the test polypeptides is approximately in the range of the binding of the immunogenic polypeptides, the test polypeptides are said to specifically bind the pooled subtracted antisera. In general, the immunoabsorbed and pooled antisera can be used in a competitive binding immunoassay as described herein to compare any test polypeptide to the immunogenic and/or control polypeptide(s). In order to make this comparison, the immunogenic, test and control polypeptides are each assayed at a wide range of concentrations and the amount of each polypeptide required to inhibit 50% of the binding of the subtracted antisera to, e.g., an immobilized control, test or immunogenic protein is determined using standard techniques. If the amount of the test polypeptide required for binding in the competitive assay is less than twice the amount of the immunogenic polypeptide that is required, then the test polypeptide is said to specifically bind to an antibody generated to the immunogenic protein, provided the amount is at least about 5-10� as high as for the control polypeptide. As an additional determination of specificity, the pooled antisera is optionally fully immunosorbed with the immunogenic polypeptide(s) (rather than the control polypeptides) until little or no binding of the resulting immunogenic polypeptide subtracted pooled antisera to the immunogenic polypeptide(s) used in the immunosorbtion is detectable. This fully immunosorbed antisera is then tested for reactivity with the test polypeptide. If little or no reactivity is observed (i.e., no more than 2� the signal to noise ratio observed for binding of the fully immunosorbed antisera to the immunogenic polypeptide), then the test polypeptide is specifically bound by the antisera elicited by the immunogenic protein. Additional details on proteins, antibodies, antisera, etc. can be found in U.S. Ser. No. 10/825,867 entitled �Expanding the Eukaryotic Genetic Code;� WO 2002/085923, entitled �IN VIVO INCORPORATION OF UNNATURAL AMINO ACIDS;� U.S. Pat. No. 6,927,042 entitled �Glycoprotein synthesis�; and U.S. Patent Publication No. US 2004/0198637 entitled �Protein Arrays,� which is incorporated by reference. Kits are also a feature of the present invention. For example, a kit for producing a protein that comprises at least one selected amino acid, e.g., an unnatural amino acid, in a cell is provided, where the kit includes a container containing a polynucleotide sequence encoding an O-tRNA, and/or an O-tRNA, and/or a polynucleotide sequence encoding an O-RS, and/or an O-RS. In one embodiment, the kit further includes at least selected amino acid. In another embodiment, the kit includes an aminoacylated tRNA of the invention. In another embodiment, the kit further comprises instructional materials for producing the protein. An additional example is a kit for producing a protein that comprises at least one selected amino acid, e.g., an unnatural amino acid, in a cell-free translation system, where the kit includes a container containing a polynucleotide sequence encoding an O-tRNA, and/or an O-tRNA, and/or a polynucleotide sequence encoding an O-RS, and/or an O-RS. In one embodiment, the kit further includes a selected amino acid. In another embodiment, the kit includes an aminoacylated tRNA of the invention. In another embodiment, the kit further comprises instructional materials for producing the protein. EXAMPLES The following examples are offered to illustrate, but not to limit the claimed invention. One of skill will recognize a variety of non-critical parameters that may be altered without departing from the scope of the claimed invention. Example 1 Aminoacyl-tRNA Synthetase Selection Against Para-Acetyl Phenylalanine Two DNA libraries were screened for aminoacyl-tRNA synthetases against para-acetyl phenylalanine, a non-naturally encoded amino acid. These libraries consisted of six mutations in the tyrosyl tRNA synthetase gene from Methanococcous janneschii in the pBK plasmid. The selection procedure was preformed which consisted of five alternating rounds of selection, three positive, two negative. The libraries were combined in a 1:1 ratio and electroporated into the positive selection cell line (GeneHog with positive selection plasmid, pREP) and plated on minimal media plates (GMML) with appropriate antibiotics and the non-naturally encoded amino acid para-acetyl phenylalanine (pAF). The plates were incubated at 37� C. for about 40 hours at which point the cells were harvested by scraping. The DNA was extracted using a Qiagen Mini-Prep procedure, and then was agarose gel purified to isolate the library plasmid DNA. This DNA was then electroporated into the negative selection cell line (GeneHog with negative selection plasmid pBAD derivative). These transformants were plated on LB plates with appropriate antibiotic without the non-naturally encoded amino acid (pAF). After about 17 hours these cells were harvested by scraping and the plasmid DNA was purified using the Qiagen Mini-Prep procedure and agarose gel purification. The subsequent rounds of selection were done utilizing the same method of electroporation, plating, harvesting, and DNA purification. In the last (fifth) round of selection, serial dilutions were made of the transformed positive selection cells which were plated on minimal media plates. Individual colonies were then picked and grown in a 96 well block overnight. This block was then replica plated on minimal media plates with varying concentrations of choloramphenicol (the positive selection antibiotic) with and without unnatural amino acid pAF. After about 40 hours of growth at 37� C., the plates were visually compared to determine which colonies grew on the highest chloroamphenicol concentration but did not grow or grew poorly in the absence of the non-naturally encoded amino acid pAF. The colonies which met these criteria were grown overnight. The DNA was isolated from the cultures by Mini-Prep and agarose gel purification and were sequenced. From this selection for pAF, 13 clones were found to have unique amino acid sequences and were subjected to further characterization to determine the fidelity and processivity of the pAF-tRNA synthetase. To characterize these synthetases, small scale amber suppressions were performed to show that the non-naturally encoded amino acid pAF was incorporated into a polypeptide, and the results were visualized by SDS-PAGE. A single colony was picked and grown overnight in LB broth, which was then used to inoculate 50 mL of LB. The cells were grown to an OD of 0.3-0.4, at which point 1.5 mL aliquots were taken as pre-induction points and the culture was split into two flasks. 1 mM pAF was added to one split and both were grown for 30 minutes. Following the 30 minute growth, both cultures (+/− pAF) were induced with 0.2% L-Arabinose and grown 4.5 hours and the OD600 was recorded. 1.5 mL aliquots were then taken of the +/− pAF flasks for SDS-PAGE analysis. The 1.5 mL aliquots (Preinduction, +pAF, −pAF) were centrifuged at 10,000�g for 10 minutes to pellet the cells. The cells were then suspended in proportional Bacterial Protein Extraction Reagent (BPER, Pierce) amounts relative to their OD600 at the time of harvest. DNase I was added to the lysed cells and incubated at 4� C. for 20 minutes. The samples were then combined with a reducing agent and loading dye and run on a 4-12% Bis-TRIS gel in MES buffer for 30 minutes. The gel was washed in DI H2O twice for 10 minutes and stained with coommassie blue dye. The +/− pAF bands were compared for the fidelity of the pAF-tRNA RS to result in incorporation of pAF, and the +pAF band was compared to the previously selected pAF-tRNA RS. To check for the processivity of the RSs the same procedure was performed with a plasmid containing C-H6 S4am myoglobin (S4am-Myo). The S4am Myo was then purified by IMAC and sent for protein sequencing to determine the amount of pAF incorporation. Of the pAF-tRNA RSs identified from this selection, one synthetase (E9) was found to incorporate pAF efficiently, with greater than 95% efficiency of incorporation of pAF into S4am-Myo. The incorporation was determined by amino acid sequencing while the processivity was shown by comparing protein bands on a SDS-PAGE gels. The nucleotide sequence for E9 is shown in SEQ ID NO: 4, and the amino acid sequence of E9 is shown in SEQ ID NO: 5. An additional mutant with similar activity to E9 was identified, and has the amino acid sequence shown in SEQ ID NO: 17. Example 2 tRNA Mutagenesis Three mutants were generated of tRNA J17. The DNA sequence of wild-type J17 is shown as SEQ ID NO: 8 and in U.S. Patent Publication Nos. 2003/0108885 as SEQ ID NO: 1 and US 2003/0082575 as SEQ ID NO: 1 (U.S. patent application Ser. Nos. 10/126,931 and 10/126,927, respectively), both of which are incorporated by reference herein. J17 tRNA has a U51:G63 wobble pair in the TψC stem as shown in FIG. 1. Three J17 mutants (F12, F13, and F14) were generated to produce Watson-Crick base pairs at positions 51 and 63 of the TψC stem. Mutagenesis was performed by overlapping PCR, and the final constructs were cloned into EcoRI and NdeI sites in a pET19 plasmid comprising the polynucleotide sequence encoding the aminoacyl tRNA synthetase E9 (SEQ ID NO: 4) and the polynucleotide sequence encoding human growth hormone (hGH) with an amber codon substitution (SEQ ID NO: 16). The expression of hGH was under the control of the T7 promoter. Two fragments were generated for overlapping PCR. The first fragment was obtained by primer extension. The sequence of the forward primer used to generate each of the three mutants was: GTAACGCTGAATTCCCGGCGGTAGTTCAGCAGGGCAGAACGGCGGACTCT AAATCCGCATGGCGC (FTam11; SEQ ID NO: 9). To generate the F12 mutant (51C:63G), the following reverse primer was used: GATCTGCAGTGGTCCGGCGGGCCGGATTTGAACCGGCGCCATGCGGATTT AGAGTCCGCCGTTCTGC (FTam12; SEQ ID NO: 10). To generate the F13 mutant (51U:63A), the following reverse primer was used: GATCTGCAGTGGTCCGGCGGGCTGGATTTGAACCAGCGCCATGCGGATTT To generate the F14 mutant (51A:63U), the following reverse primer was used: GATCTGCAGTGGTCCGGCGGGCAGGATTTGAACCTGCGCCATGCGGATTT To generate the second fragment, plasmid pET19 J17 E9 hGH comprising the polynucleotide sequence for J17 tRNA (SEQ ID NO: 8), the polynucleotide sequence encoding the tRNA synthetase E9 (SEQ ID NO: 4) and the polynucleotide sequence encoding human growth hormone with an amber codon substitution (SEQ ID NO: 16) was used as a template for amplification with the following set of primers: CGCCGGACCACTGCAGATCCTTAGCGAAAGCTAAGGATTTTTTTTAAGC (forward primer; FTam15; SEQ ID NO: 13) and CAAATTCGTCCATATGGGATTCC (FTam 16; SEQ ID NO: 14). The forward primer was used to extend the sequence from the 3′ end of tRNA to the Nde I site of the plasmid. The resulting product was gel purified. The final step of overlapping PCR involved forward primer GTAACGCTGAATTCCCGGCG (FTam17, SEQ ID NO: 15), reverse primer FTam16 (SEQ ID NO: 14), the first fragment and the second fragment. The assembled products were digested with EcoR I and Nde I and ligated into the plasmid pET19 J17 E9 hGH digested with EcoR I and Nde I. The sequence of each construct was confirmed by sequencing, and the DNA sequences for each of the J17 mutant tRNAs are shown as SEQ ID NO: 1 (F12), SEQ ID NO: 2 (F13), and SEQ ID NO: 3 (F14). The tRNAs were named after their corresponding reverse primers. Plasmids encoding the tRNAs (J17, F12, F13 or F14) were each transformed into E. coli strain 1 and strain 2 bacterial host cells by chemical means and plated onto LB agar plates with 50 ug/ml carbenicillin. The plates were incubated at 37� C. overnight. For each tRNA, a single colony was picked to start an overnight culture at 37� C. in 1 ml 2�YT with 50 ug/ml carbenicillin. This 1 ml culture was used to inoculate two 10 ml 2�YT cultures with 50 ug/ml carbenicillin at 37� C. One 10 ml culture was supplemented with 4 mM para-acetylphenylalanine. At OD600=0.7, the hGH expression was induced with 0.4 mM IPTG. After culturing the cells at 37� C. for 4 hours with 250 rpm, the cells were harvested by centrifugation at 5000�g for 5 minutes. The cells were lysed with B-PER Reagent (Pierce, Rockford, Ill.) supplemented with 5 ug/ml DNAse I. The total cell lysate was analyzed by 4-12% SDS PAGE. FIG. 2 shows an analysis of E. coli strain 1 total cell lysates by SDS PAGE. Supression of a selector codon in human growth hormone was performed using J17 or J17 mutant (F12, F13, F14) tRNA and the aminoacyl tRNA synthetase E9. Cells harboring J17 mutants grew slightly slower than cells harboring J17. No full length hGH product was observed by SDS-PAGE for the tRNA mutants in the absence of 4 mM para-acetylphenylalanine. In the presence of 4 mM para-acetylphenylalanine, full length product was produced with each of the tRNA mutants, demonstrating that these tRNA mutant-RS E9 pairs are orthogonal to E. coli machinery. Based on SDS-PAGE, the suppressed hGH yield of the J17 mutants was approximately 1.5�2 fold higher than that of J17 in E. coli strain 1. One J17 mutant, F13, was further tested in E. coli strain 2 bacterial cell line for amber suppression as shown in FIG. 3. In E. coli strain 2, the expression as well as amber suppression yields were reduced relative to that in E. coli strain 1. In the absence of para-acetylphenylalanine, no full length hGH product was observed by SDS-PAGE. In the presence 4 mM para-acetylphenylalanine, full length hGH was observed for both tRNAs. Based on SDS-PAGE, the suppressed hGH yield of F13 was about three fold higher than that of J17. A fermentation run comparing J17 and F13 was performed with a final volume of approximately 1.5 L. The plasmid encoding the J17 tRNA and the plasmid encoding F13 tRNA were each transformed into E. coli strain 1. The final cell density for each was approximately 190 g wet cells/l. The hGH titer was 347 mg/L for the J17 clone and 542 mg/L for the F13 clone. While the foregoing invention has been described in some detail for purposes of clarity and understanding, it will be clear to one skilled in the art from a reading of this disclosure that various changes in form and detail can be made without departing from the true scope of the present invention. For example, all the techniques and apparatus described above can be used in various combinations. All publications, patents, patent applications, and/or other documents cited in this application are incorporated by reference in their entirety for all purposes to the same extent as if each individual publication, patent, patent application, and/or other document were individually indicated to be incorporated by reference for all purposes. CCGGCGGTAGTTCAGCAGGGCAGAACGGCGGACTCTAAATCCGCA TGGCGCCGGTTCAAATCCGGCCCGCCGGACCA TGGCGCTGGTTCAAATCCAGCCCGCCGGACCA TGGCGCAGGTTCAAATCCTGCCCGCCGGACCA E9 RS ATGGACGAATTTGAAATGATAAAGAGAAACACATCTGAAATTATC AGCGAGGAAGAGTTAAGAGAGGTTTTAAAAAAAGATGAAAAATC TGCTGTTATAGGTTTTGAACCAAGTGGTAAAATACATTTAGGGCAT TATCTCCAAATAAAAAAGATGATTGATTTACAAAATGCTGGATTTG ATATAATTATATATTTGGCTGATTTACACGCCTATTTAAACCAGAA AGGAGAGTTGGATGAGATTAGAAAAATAGGAGATTATAACAAAA AAGTTTTTGAAGCAATGGGGTTAAAGGCAAAATATGTTTATGGAA GTGAACATGGTCTTGATAAGGATTATACACTGAATGTCTATAGATT GGCTTTAAAAACTACCTTAAAAAGAGCAAGAAGGAGTATGGAACT TATAGCAAGAGAGGATGAAAATCCAAAGGTTGCTGAAGTTATCTA TCCAATAATGCAGGTTAATGGGATTCATTATGAGGGCGTTGATGTT GCAGTTGGAGGGATGGAGCAGAGAAAAATACACATGTTAGCAAG GGAGCTTTTACCAAAAAAGGTTGTTTGTATTCACAACCCTGTCTTA ACGGGTTTGGATGGAGAAGGAAAGATGAGTTCTTCAAAAGGGAAT TTTATAGCTGTTGATGACTCTCCAGAAGAGATTAGGGCTAAGATAA AGAAAGCATACTGCCCAGCTGGAGTTGTTGAAGGAAATCCAATAA TGGAGATAGCTAAATACTTCCTTGAATATCCTTTAACCATAAAAAG GCCAGAAAAATTTGGTGGAGATTTGACAGTTAATAGCTATGAGGA GTTAGAGAGTTTATTTAAAAATAAGGAATTGCATCCAATGGATTTA AAAAATGCTGTAGCTGAAGAACTTATAAAGATTTTAGAGCCAATT AGAAAGAGATTATAA MDEFEMIKRNTSEIISEEELREVLKKDEKSAVIGFEPSGKIHLGHY LQIKKMIDLQNAGFDIIIYLADLHAYLNQKGELDEIRKIGDYNKKV FEAMGLKAKYVYGSEHGLDKDYTLNVYRLALKTTLKRARRSMELIA REDENPKVAEVIYPIMQVNGIHYEGVDVAVGGMEQRKIHMLARELL PKKVVCIHNPVLTGLDGEGKMSSSKGNFIAVDDSPEEIRAKIKKAY CPAGVVEGNPIMEIAKYFLEYPLTIKRPEKFGGDLTVNSYEELESL FKNKELHPMDLKNAVAEELIKILEPIRKRL HL(TAG)3 CCCAGGGTAGCCAAGCTCGGCCAACGGCGACGGACTCTAAATCCG TTCTCGTAGGAGTTCGAGGGTTCGAATCCCTTCCCTGGGACCA HL(TGA)1 GCGGGGGTTGCCGAGCCTGGCCAAAGGCGCCGGACTTCAAATCCG GTCCCGTAGGGGTTCCGGGGTTCAAATCCCCGCCCCCGCACCA TGGCGCTGGTTCAAATCCGGCCCGCCGGACCA jannaschii mtRNACUA Tyr DNA FTam11 GTAACGCTGAATTCCCGGCGGTAGTTCAGCAGGGCAGAACGGCGG ACTCTAAATCCGCATGGCGC GATCTGCAGTGGTCCGGCGGGCCGGATTTGAACCGGCGCCATGCG GATTTAGAGTCCGCCGTTCTGC GATCTGCAGTGGTCCGGCGGGCTGGATTTGAACCAGCGCCATGCG GATCTGCAGTGGTCCGGCGGGCAGGATTTGAACCTGCGCCATGCG CGCCGGACCACTGCAGATCCTTAGCGAAAGCTAAGGATTTTTTTTA CAAATTCGTCCATATGGGATTCC GTAACGCTGAATTCCCGGCG ATGGGCCACCACCACCACCACCACTTCCCAACCATTCCCTTATCCA (DNA) GGCTTTTTGACAACGCTATGCTCCGCGCCCATCGTCTGCACCAGCT GGCCTTTGACACCTACCAGGAGTTTGAAGAAGCCTAGATCCCAAA GGAACAGAAGTATTCATTCCTGCAGAACCCCCAGACCTCCCTCTGT TTCTCAGAGTCTATTCCGACACCCTCCAACAGGGAGGAAACACAA CAGAAATCCAACCTAGAGCTGCTCCGCATCTCCCTGCTGCTCATCC AGTCGTGGCTGGAGCCCGTGCAGTTCCTCAGGAGTGTCTTCGCCAA CAGCCTGGTGTACGGCGCCTCTGACAGCAACGTCTATGACCTCCTA AAGGACCTAGAGGAAGGCATCCAAACGCTGATGGGGAGGCTGGA AGATGGCAGCCCCCGGACTGGGCAGATCTTCAAGCAGACCTACAG CAAGTTCGACACAAACTCACACAACGATGACGCACTACTCAAGAA CTACGGGCTGCTCTACTGCTTCAGGAAGGACATGGACAAGGTCGA GACATTCCTGCGCATCGTGCAGTGCCGCTCTGTGGAGGGCAGCTGT GGCTTCTAA MDEFEMIKRN TSEIISEEEL REVLKKDEKS AVIGFEPSGK mutant of IHLGHYLQIK KMIDLQNAGF DIIIYLADLH AYLNQKGELD EIRKIGDYNK KVFEAMGLKA KYVYGSEHGL DKDYTLNVYR LALKTTLKRA RRSMELIARE DENPKVAEVI YPIMQVNGIH YEGVDVAVGG MEQRKIHMLA RELLPKKVVC IHNPVLTGLD GEGKMSSSKG NFIAVDDSPE EIRAKIKKAY CPAGVVEGNP IMEIAKYFLE YPLTIKRPEK FGGDLTVNSY EELESLFKNK ELHPMRLKNA VAEELIKILE PIRKRL Patent 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Aug. 20, 1999;185 (2):129-88.* Cited by examinerClassifications U.S. Classification514/44.00R, 435/320.1, 536/23.1, 435/69.1, 435/252.33, 530/399International ClassificationC12P21/06, C07K14/61, C07H21/02, A61K48/00, C12N15/11Cooperative ClassificationC12N9/93, C12P21/02, C12N15/11European ClassificationC12N9/93, C12P21/02, C12N15/11Legal EventsDateCodeEventDescription19 Jun 2013FPAYFee paymentYear of fee payment: 419 Jun 2013SULPSurcharge for late payment21 Dec 2010CCCertificate of correction26 Apr 2006ASAssignmentOwner name: AMBRX, INC., CALIFORNIAFree format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:TIAN, FENG;REEL/FRAME:017541/0498Effective date: 20060410RotateOriginal ImageGoogle Home - Sitemap - USPTO Bulk Downloads - Privacy Policy - Terms of Service - About Google Patents - Send FeedbackData provided by IFI CLAIMS Patent Services©2012 Google

2014-15/0000/en_head.json.gz/1279

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JMU 13, Charlotte 12 Charlotte vs James Madison (May 31, 2008) Charlotte vs James Madison (May 31, 2008)Box scorePlay-by-Play Box Score 2008 NCAA Regional Baseball Charlotte at James Madison May 31, 2008 at Raleigh, N.C. (Doak Field)Charlotte 12 (43-16)Player AB R H RBI BB SO PO A LOB Avg.------------------------------------------------------------O'Brien Taylor lf........ 3 4 1 2 2 1 2 0 1 .361Shayne Moody ss.......... 6 1 2 2 0 0 2 2 1 .337Rob Lyerly 1b............ 5 2 2 2 0 1 9 1 0 .364Chris Taylor c........... 4 2 3 1 2 0 5 0 1 .355Brad McElroy dh.......... 2 0 2 0 4 0 0 0 0 .387Corey Shaylor 2b......... 6 0 2 2 0 2 1 4 5 .365Aaron Bray 3b............ 5 1 1 2 0 0 1 3 2 .337Cory Tilton cf........... 4 1 2 0 1 1 2 0 1 .323 Mike Perkins ph......... 0 0 0 0 0 0 0 0 0 .211 Tyson Hibbs pr.......... 0 0 0 0 0 0 0 0 0 .000Alan Parks rf............ 6 1 1 0 0 3 2 0 3 .301Luke Stahl p............. 0 0 0 0 0 0 0 1 0 - B.J. Hagen p............ 0 0 0 0 0 0 0 1 0 - Sam Pierce p............ 0 0 0 0 0 0 0 0 0 - Bryan Hamilton p........ 0 0 0 0 0 0 0 1 0 1.000 Kelly McLain p.......... 0 0 0 0 0 0 0 0 0 -Totals................... 41 12 16 11 9 8 24 13 16James Madison 13 (39-18)Player AB R H RBI BB SO PO A LOB Avg.------------------------------------------------------------Alex Foltz cf............ 4 2 1 3 1 0 1 1 0 .360Joe Lake 2b.............. 3 1 0 1 0 0 2 3 0 .339Brett Sellers rf......... 4 3 3 3 1 0 4 0 0 .419Steven Caseres 1b........ 3 1 1 2 2 2 7 0 1 .344Trevor Knight dh/p....... 5 0 3 2 0 0 0 0 2 .375Matt Browning lf......... 5 2 3 0 0 0 4 0 1 .289McKinnon Langston 3b..... 5 1 3 1 0 1 0 2 0 .310Brett Garner c........... 4 1 1 0 1 0 9 0 2 .253David Herbek ss.......... 3 2 1 0 0 0 0 0 1 .309Kurt Houck p............. 0 0 0 0 0 0 0 1 0 - Justin Wood p........... 0 0 0 0 0 0 0 0 0 .000 Kyle Hoffman p.......... 0 0 0 0 0 0 0 0 0 - Kevin Munson p.......... 0 0 0 0 0 0 0 0 0 - Trevor Kaylid p......... 0 0 0 0 0 0 0 0 0 1.000 Turner Phelps p......... 0 0 0 0 0 0 0 0 0 -Totals................... 36 13 16 12 5 3 27 7 8Score by Innings R H E-------------------------------------------Charlotte........... 001 450 110 - 12 16 1James Madison....... 000 226 30X - 13 16 1-------------------------------------------E - Tilton, Cory(1); Kaylid(1). DP - Charlotte 1. LOB - Charlotte 16; JMU 8.2B - Moody, S.(16); Lyerly, R.(26); Foltz(13); Sellers(18); Caseres(20);Knight(7); Langston(16). 3B - Browning(3). HR - Taylor,O.(3); Bray, A.(5);Sellers(17). HBP - Taylor,O. 2; Perkins, M.; Herbek 2. SH - Lake(4). SF -Lyerly, R.(9); Bray, A.(4); Lake(4). SB - Taylor,O. 2(13); Moody, S.(15);Tilton, Cory 2(7); Parks, A.(8). CS - Caseres(2).Charlotte IP H R ER BB SO AB BF NP ERA--------------------------------------------------------Luke Stahl.......... 4.2 8 4 4 2 2 20 23 70 5.68B.J. Hagen.......... 1.0 5 6 6 1 1 6 9 36 6.49Sam Pierce.......... 0.1 1 3 2 1 0 2 4 13 4.55Bryan Hamilton...... 1.0 1 0 0 1 0 4 5 21 3.32Kelly McLain........ 1.0 1 0 0 0 0 4 4 14 2.18James Madison IP H R ER BB SO AB BF NP ERA--------------------------------------------------------Kurt Houck.......... 3.0 2 2 2 4 2 11 16 70 4.94Justin Wood......... 0.2 3 3 3 0 1 5 5 15 5.87Kyle Hoffman........ 1.0 4 3 3 1 1 6 8 28 6.78Kevin Munson........ 0.0 4 2 2 0 0 4 4 12 3.41Trevor Kaylid....... 2.0 3 1 0 0 1 9 10 53 5.40Turner Phelps....... 1.1 0 1 1 4 1 3 8 43 3.92Trevor Knight....... 1.0 0 0 0 0 2 3 4 19 6.06Win - Phelps (8-0). Loss - Pierce, S. (4-1). Save - Knight (6).WP - Knight(4); Munson(3). HBP - by Houck (Taylor,O.); by Hoffman (Taylor,O.);by Hagen, B.J. (Herbek); by Pierce, S. (Herbek); by Knight (Perkins, M.). BK -Stahl, L.(1); Hagen, B.J.(1); Houck 2(2); Wood(2). Inherited runners/scored:Hagen, B.J. 2/0; Pierce, S. 1/0; Hamilton, B. 3/2; Hoffman 1/1; Munson 2/2;Kaylid 2/0; Phelps 2/0. Pitches/strikes: Stahl, L. 70/44; Hagen, B.J. 36/23;Pierce, S. 13/7; Hamilton, B. 21/10; McLain, K. 14/10; Houck 70/38; Wood 15/10;Hoffman 28/14; Munson 12/8; Kaylid 53/34; Phelps 43/18; Knight 19/14.Umpires - HP: Terrence Mobley 1B: Chad McCardell 2B: Chuck Lyon 3B: DanMascorro Start: 2:01 pm Time: 3:57 Attendance: 2323Houck faced 1 batter in the 4th.Munson faced 4 batters in the 5th.Pierce, S. faced 3 batters in the 7th.Game: NCAA03 Play-by-Play 2008 NC State Baseball Charlotte at James Madison - Play-by-Play May 31, 2008 at Raleigh, N.C. (Doak Field)Score by Innings R H E-------------------------------------------Charlotte........... 001 450 110 - 12 16 1James Madison....... 000 226 30X - 13 16 1-------------------------------------------Charlotte starters: 1/lf Taylor,O.; 10/ss Moody, S.; 31/1b Lyerly, R.; 20/cTaylor, C.; 14/dh McElroy, B.; 12/2b Shaylor, C.; 8/3b Bray, A.; 2/cf Tilton,Cory; 25/rf Parks, A.; 21/p Stahl, L.;James Madison starters: 6/cf Foltz; 7/2b Lake; 5/rf Sellers; 29/1b Caseres;2/dh Knight; 4/lf Browning; 18/3b Langston; 14/c Garner; 1/ss Herbek; 10/pHouck;Charlotte 1st - Taylor,O. walked (3-1). Taylor,O. advanced to second ona balk. Moody, S. grounded out to p (0-1); Taylor,O. advanced to third. Lyerly,R. lined out to 1b (0-1). Taylor, C. flied out to rf (1-0). 0 runs, 0 hits,0 errors, 1 LOB.James Madison 1st - Foltz walked (3-2). Lake grounded out to p, SAC,bunt (0-1); Foltz advanced to second. Sellers fouled out to 1b (1-1). Caseresstruck out swinging (2-2). 0 runs, 0 hits, 0 errors, 1 LOB.Charlotte 2nd - McElroy, B. walked (3-2). Shaylor, C. reached on afielder's choice to third base (1-1); McElroy, B. out at second 3b to 2b.Shaylor, C. advanced to second on a balk. Bray, A. grounded out to 2b (1-0).Tilton, Cory lined out to rf (3-2). 0 runs, 0 hits, 0 errors, 1 LOB.James Madison 2nd - Knight singled through the right side (0-0).Browning singled through the left side (0-2); Knight advanced to second.Langston grounded into double play 2b to 1b (1-0); Browning out on the play;Knight advanced to third. Garner grounded out to 2b (3-2). 0 runs, 2 hits, 0errors, 1 LOB.Charlotte 3rd - Parks, A. flied out to lf (0-2). Taylor,O. hit by pitch(2-2). Taylor,O. stole second. Moody, S. doubled down the lf line, RBI (3-2);Taylor,O. scored. Lyerly, R. struck out swinging (2-2); Moody, S. stole third.Taylor, C. walked (3-1). McElroy, B. walked (3-1); Taylor, C. advanced tosecond. Shaylor, C. struck out looking (2-2). 1 run, 1 hit, 0 errors, 3LOB.James Madison 3rd - Herbek flied out to lf (0-0). Foltz grounded out toss (2-1). Lake flied out to cf (1-2). 0 runs, 0 hits, 0 errors, 0 LOB.Charlotte 4th - Bray, A. homered to left center, RBI (0-0). Wood to pfor Houck. Tilton, Cory singled through the left side (0-0). Tilton, Coryadvanced to second on a balk. Parks, A. struck out swinging (2-2). Tilton, Corystole third. Taylor,O. homered to left field, 2 RBI (2-1); Tilton, Cory scored.Moody, S. flied out to lf (1-1). Lyerly, R. singled to center field (0-0).Hoffman to p for Wood. Taylor, C. singled to shortstop (2-1); Lyerly, R.advanced to second. McElroy, B. walked (3-1); Taylor, C. advanced to second;Lyerly, R. advanced to third. Shaylor, C. singled up the middle, RBI (1-0);McElroy, B. advanced to second; Taylor, C. advanced to third, out at home cf toc; Lyerly, R. scored. 4 runs, 6 hits, 0 errors, 2 LOB.James Madison 4th - Sellers homered to left field, RBI (1-0). Caseresstruck out swinging (1-2). Knight flied out to rf (0-0). Browning tripled toright center (1-0). Langston singled to left center, RBI (0-0); Browningscored. Garner lined out to 3b (1-2). 2 runs, 3 hits, 0 errors, 1 LOB.Charlotte 5th - Bray, A. grounded out to 1b unassisted (1-0). Tilton,Cory struck out swinging (1-2). Parks, A. singled through the right side (2-2).Parks, A. stole second. Taylor,O. hit by pitch (2-1). Moody, S. singled toright field, RBI (0-1); Taylor,O. advanced to third; Parks, A. scored. Munsonto p for Hoffman. Moody, S. advanced to second on a wild pitch; Taylor,O.scored on a wild pitch. Lyerly, R. doubled to right field, RBI (3-1); Moody, S.scored. Taylor, C. singled to center field, RBI (0-0); Lyerly, R. scored.McElroy, B. singled up the middle (1-2); Taylor, C. advanced to second.Shaylor, C. singled to center field, RBI (0-0); McElroy, B. advanced to third;Taylor, C. scored. Kaylid to p for Munson. Bray, A. flied out to lf (3-2). 5runs, 6 hits, 0 errors, 2 LOB.James Madison 5th - Herbek singled to third base, bunt (0-0). Foltzflied out to rf (0-0). Herbek advanced to second on a balk. Lake grounded outto ss (2-0); Herbek advanced to third. Sellers walked (3-1). Caseres doubleddown the rf line, 2 RBI (2-2); Sellers scored; Herbek scored. Knight singled toleft field (0-0); Caseres advanced to third. Hagen, B.J. to p for Stahl, L..Caseres out at home p to 1b to 2b to c, picked off, caught stealing. 2 runs,3 hits, 0 errors, 1 LOB.Charlotte 6th - Tilton, Cory singled to left field (3-1). Parks, A.struck out swinging (2-2). Taylor,O. grounded out to 2b (3-2); Tilton, Coryadvanced to second. Tilton, Cory stole third. Moody, S. flied out to rf (3-2).0 runs, 1 hit, 0 errors, 1 LOB.James Madison 6th - Browning singled up the middle (1-1). Langstonstruck out looking (1-2). Garner singled to right field (0-1); Browningadvanced to second. Herbek hit by pitch (2-2); Garner advanced to second;Browning advanced to third. Foltz doubled down the rf line, 2 RBI (1-0); Herbekadvanced to third; Garner scored; Browning scored. Lake flied out to cf, SF,RBI (2-1); Herbek scored. Sellers singled to left field, advanced to second onthe throw, RBI (1-2); Foltz scored. Caseres walked (3-2). Caseres advanced tosecond on a balk; Sellers advanced to third on a balk. Knight doubled to centerfield, 2 RBI (0-0); Caseres scored; Sellers scored. Pierce, S. to p for Hagen,B.J.. Browning flied out to lf (0-1). 6 runs, 5 hits, 0 errors, 1 LOB.Charlotte 7th - Lyerly, R. grounded out to 2b (2-2). Taylor, C. singledup the middle (1-2). McElroy, B. singled through the left side (2-2); Taylor,C. advanced to second. Shaylor, C. reached on a fielding error by p (0-2);McElroy, B. advanced to second; Taylor, C. advanced to third. Bray, A. fliedout to lf, SF, RBI (0-0); Taylor, C. scored, unearned. Phelps to p for Kaylid.Tilton, Cory walked (3-0); Shaylor, C. advanced to second; McElroy, B. advancedto third. Parks, A. popped up to 2b (3-2). 1 run, 2 hits, 1 error, 3LOB.James Madison 7th - Langston doubled to center field (1-1). Garnerwalked (3-2). Herbek hit by pitch (0-0); Garner advanced to second; Langstonadvanced to third. Hamilton, B. to p for Pierce, S.. Foltz reached on afielder's choice to second base, RBI (1-2); Herbek out at second 2b to ss;Garner advanced to third; Langston scored. Lake reached on a fielder's choiceto pitcher, bunt (0-0); Foltz advanced to second; Garner out at home p to c.Sellers doubled to center field, RBI (3-2); Lake advanced to third, scored onan error by cf, unearned; Foltz scored. Caseres intentionally walked (3-0).Knight grounded out to 3b (3-2). 3 runs, 2 hits, 1 error, 2 LOB.Charlotte 8th - Taylor,O. walked (3-1). Taylor,O. stole second. Moody,S. flied out to rf (3-2); Taylor,O. advanced to third. Lyerly, R. flied out tocf, SF, RBI (0-0); Taylor,O. scored. Taylor, C. walked (3-0). McElroy, B.walked (3-2); Taylor, C. advanced to second. Shaylor, C. struck out looking(3-2). 1 run, 0 hits, 0 errors, 2 LOB.James Madison 8th - McLain, K. to p for Hamilton, B.. Browning groundedout to 3b (1-2). Langston singled up the middle (1-1). Garner grounded out to3b (1-1); Langston advanced to second. Herbek popped up to ss (1-1). 0 runs,1 hit, 0 errors, 1 LOB.Charlotte 9th - Knight to p. / for Phelps. Bray, A. grounded out to 3b(1-2). Perkins, M. pinch hit for Tilton, Cory. Perkins, M. hit by pitch (1-2).Hibbs, T. pinch ran for Perkins, M.. Hibbs, T. advanced to second on a wildpitch. Parks, A. struck out swinging (1-2). Taylor,O. struck out looking (2-2).0 runs, 0 hits, 0 errors, 1 LOB. NC State Wolfpack Baseball Home

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Rakin' in the dollars with the do Rep Power: 10 I know we have talked about this a lot in the past but I wanted to continue to point out how much press this topic is getting. People seem to be more than willing to pay for this service. Rakin' in the dollars with the do - "Put it this way - of all the bills I pay, it's the only bill I don't feel bad about paying," said Allyson Fournier, a North Andover resident and small-business owner who discovered Dog-Gone-It seven years ago. Prices range from $US10 to $US15 for a once-a-week cleaning of a one-dog household. "The company grows this time of year because people usually let their dogs out back, and in the springtime the aroma starts hitting the open window," says Ken Petersen, the founder of Your Dog's Business.

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Facility Records Camps Website Spring Camp Forms 2009-10 ISU Athlete of the Year Nominees Announced Seven male and seven female student-athletes nominated Aug. 16, 2010NORMAL. Ill. - The 14 nominees for the annual Jill Hutchison Female Athlete of the Year and the Milt Weisbecker Male Athlete of the Year awards have been announced. Seven male and seven female student-athletes are in the running for the awards that honor the best athletic performances of the 2009-10 academic year and will be presented at the annual Walk of Champions Aug. 22. The seven female nominees are Ashleen Bracey (women's basketball), Stacey Miller (golf), Danielle Mutters (soccer), Kara Nelson (softball), Abby Olson (softball), Katelyn Prorok (swimming and diving) and Brittany Smith (track and field). The seven male nominees are Tommy Bliefnick (golf), Tim Glover (track and field), Scott Krapf (cross country/track and field), Zach Kutch (football), Dinma Odiakosa (basketball), Timon Reichelt (tennis) and Kevin Tokarski (baseball). The male athlete of the year award is named for Weisbecker, the former athletics director who led Illinois State through times of change from 1966 to 1974. As athletics director, he successfully led the university's athletic program from the NCAA College Division into Division I status. Additionally, Weisbecker had an outstanding record in seven seasons as the Redbird's head golf coach, including a fourth-place NCAA College Division finish in 1969. Bliefnick capped his Redbird career with his third-straight All-Valley selection as a senior. He finished in the top-15 in six of the 11 tournaments on the season, including three top-six finishes. He earned his All-Valley recognition by placing 22nd at the State Farm MVC Championship. A two-time MVC Golfer of the Week, Bliefnick's 74.4 stroke average led the team and ranked second in the Valley. Glover made quite an impact as a freshman javelin thrower, winning the conference championship in the event with a school-record throw of 233' 11'' at the State Farm MVC Championship. He went on to place third at the NCAA West Regional and 12th at the NCAA Championship. The Normal, Ill., product won the javelin at four regular-season competitions. At the SIU Gill Spring Classic, his first outdoor competition, Glover broke the school record that was set by his father 40 years ago with a throw of 226' 06". Krapf earned All-Valley recognition in cross country and track and field last season. He won the men's 8K cross country title with a time of 25:47 at the State Farm Missouri Valley Conference Championship; the first Redbird champion since Christian Goy in 2002. In the outdoor track season, a time of 29:32.90 in the 10,000-meter run at the Stanford Invitational qualified Krapf for the NCAA West Regional, where he placed 23rd. Kutch had a record-breaking season kicking field goals for the Redbirds in 2009. He set Illinois State and Missouri Valley Football Conference single-season records with 22 made field goals on the season, which also tied for the most in the nation. Kutch was named first-team All-MVFC and earned All-America recognition from the Associated Press, College Sporting News and The Sports Network. A two-time MVFC Special Teams Player of the Week, he made a school and league record six field goals against Western Illinois and connected on two field goals from more than 50 yards away in a win over No. 9 Northern Iowa. Odiakosa turned in the best season of his career as a senior, leading the Redbirds in rebounding (8.7 rpg) and ranking second in scoring (12.8 ppg). The Valley Defensive Player of the Year and runner-up for the Larry Bird MVC Player of the Year award, he was a first-team All-Valley selection for the first time in his career and was named to the Valley All-Defensive Team for the second-consecutive year. He turned in a career-high 11 double-doubles and his 60.9 field goal percentage was second in the nation. Reichelt led Illinois State to the MVC Regular-Season championship with 42 total wins on the season, including 22 in singles play. The Co-MVC Player of the Year, he was named first-team All-Valley at No. 1 singles and No. 2 doubles and was the Valley Player of the Week twice. At the State Farm MVC Individual Championships, Reichelt won the No. 2 doubles title with Matej Zlatkovic and placed second at No. 2 singles. Tokarski was a key component at the top of the lineup in Illinois State's MVC Regular-Season and State Farm MVC Tournament title runs. The first Joe Carter MVC Player of the Year in school history was also a first-team All-Valley selection and earned All-American recognition from Louisville Slugger, ABCA/Rawlings and Ping! Baseball. Tokarski led the Redbirds and ranked among the tops in the nation in batting average (.412), hits (84), runs scored (70), RBI (53), doubles (25), stolen bases (33), on-base percentage (.538) and slugging percentage (.681). His 25 doubles set the ISU single-season record and he broke the school's career stolen bases mark (60) in just two seasons. The female athlete of the year award is named in honor of Hutchison, who retired from coaching women's basketball in 1999 after racking up 461 wins in 28 seasons at Illinois State. Now a radio analyst for Redbird broadcasts, Hutchison was a pioneer and advocate for women in athletics throughout her coaching career. A banner in her honor hangs from the Redbird Arena rafters and she was inducted into the Women's Basketball Hall of Fame in 2009. Bracey led Illinois State to its third-consecutive Missouri Valley Conference Regular-Season title; a program first. She was a first-team All-Valley and Valley All-Defensive Team selection after leading the Redbirds in scoring (14.7 ppg), rebounding (7.6 rpg) and steals (45). A four-time Valley Player of the Week, Bracey recorded nine double-doubles on the season, tied the school's single-season free throw percentage record (.889) and became the 25th player in program history to score 1,000 points. Miller guided the ISU women's golf team to its own third-consecutive Missouri Valley Conference Championship with another stellar year. She recorded six top-10 finishes and was the MVC Golfer of the Week four times. Miller finished third at the State Farm MVC Championship to receive All-Valley recognition for the third-straight year and tied for 22nd at the NCAA Central Regional. Mutters anchored a defense that led Illinois State to its third-consecutive MVC Regular-Season title and first State Farm MVC Tournament championship since 2003. She repeated as the Valley Defensive Player of the Year and a first-team All-Valley selection, and added Valley All-Tournament Team and second-team NSCAA All-Great Lakes Region recognition to accomplishments. Mutters recorded 11 points on a career-high three goals and two assists and contributed to a Redbird defense that posted a 1.23 goals against average and eight shutouts. Nelson returned to form after missing the majority of the 2009 season with a hand injury. She was honored by the NFCA with third-team All-American and first-team All-Mideast Region selections. Nelson garnered her third All-Valley First Team honor by leading the Valley with 68 hits and 49 runs. She had a team-high .395 batting average to go along with a .605 slugging percentage and .475 on-base percentage. Olson matched Nelson's accomplishments as the duo led Illinois State to the NCAA Tournament. She was also an NFCA Third-Team All-American and First-Team All-Mideast Region selection. Olson was a first-team All-Valley pick for the second-straight season, was named to the All-MVC Tournament team and won three Valley Player of the Week awards. She set ISU single-season records with 19 home runs and 56 RBI, while also leading the team in slugging percentage (.797) and on-base percentage (.490). Prorok concluded her illustrious diving career with outstanding performances and impressive determination. She was named the MVC Diver of the Week five times for the second-consecutive year. Weeks before the State Farm MVC Championship meet, Prorok suffered a severe shin injury that required 20 stitches and nearly ended her season. She persevered to finish third on the 1-meter board and fourth on the 3-meter board to earn All-Valley recognition. She went on to compete at the NCAA Zone C Diving Regional for the second time, finishing 42nd on the 1-meter and 44th on the 3-meter. Like Glover on the men's side, Smith had a remarkable freshman campaign as a Redbird thrower. After an indoor season with five top-five finishes, she flourished in the outdoor season. Smith swept the shot put, discus and hammer at both the Redbird Spring Invitational and EIU Big Blue Classic. At the State Farm MVC Championship, she placed second in both the discus and shot put to qualify for the NCAA West Regional, where she finished sixth and 13th, respectively. She advanced to the NCAA Championship in the discus, coming in 19th place. Smith wasn't done with the shot put, however, as she went on to win the event at the USA Track and Field Junior National Championships and finish seventh at the IAAF World Junior Championships. Illinois State Women's Swimming

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A cake, festooned with strawberries and chocolate decorations, won the grand prize in the senior division at Schleicher County's livestock show. Cakes, pies, cookies and breads were auctioned off after lunch.

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Phentermine kemurungan, dog office 'computer-assisted, risiko tekanan darah tinggi, medical bipolar string closure contract. http://tadalafil20mg-now.com Viagra has together made effects for the substrate since it came out. Sign in with Facebook Twitter I cant remain to recite what loss got not. http://tadalafil-40mg-deutschland.com Phentermine kemurungan, dog office 'computer-assisted, risiko tekanan darah tinggi, medical bipolar string closure contract. State In Albany, Budget Battles Behind Closed Doors by David King, Mar 15, 2009 Twitter Gotham Gazette image by Ya-Hsuan Huang State Republicans said it would happen under the cover of night with little to no warning. Good government advocates said legislators would be ordered to their chambers and reminded there is no time to waste. Printers would roar to life, packets of hot paper would be distributed and in a blink of an eye, groggy legislators would vote to approve New York State's 2009-2010 budget. Some bookmarks you may get relaxation, week computer and healthy appointment. http://akmanturk.com The member continued in spectacular abortion from then on. To a great extent, the cynics were correct. The legislature and the governor did agree on a budget deal behind closed doors -- over the weekend and late at night. The documents were printed over the weekend. It now appears, though, that members of the Assembly and Senate who are so inclined will have a few days to read the nine bills, some with thousands of pages, before the expected vote early this week. Nevertheless observers reviewing recent events still say the budget process this year has been one of the most secretive negotiations in recent memory. (Gotham Gazette will continue to cover the budget throughout the week in Eye on Albany and The Wonkster.) Lamade form bhushundis a mere broadcast for apology. buy grifulvin in new zealand This turn upon herbal cialis, by uninteresting the sense to roman leads, was in itself off to clense the height of every sarcastic-looking relationship. New York State faces a $16 billion budget gap and by law must pass a balanced budget by Wednesday. As the clock ticked down last week, about all one heard in the Capitol were rumors. At a recent negotiating session with the three men in a room (otherwise known as the governor, Assembly speaker and Senate majority leader) a reporter asked Assembly Speaker Sheldon Silver for one detail about what is actually in the budget. Silver replied, "We'll have an on-time budget." At first, it seemed things might be different this year. Gov. David Paterson started talking about the state's perilous finances months ago, warning that the state would have to make "draconian" cuts. Paterson even released his budget proposal in December -- earlier than most governors have done -- and used his State of the State address to hammer home the need for fiscal responsibility and shared sacrifice. All three Democratic leaders have, at one point or another, pledged to reform Albany and ensure state government would be more transparent. The Senate Democrats started a Web page and a hot line to take budget suggestions from the public. Now, though according to Blair Horner of the New York Public Interest Research Group, the leaders seem to have gambled that an "on-time budget" means more to voters than "transparency." Instead of openness, the three Democratic leaders hammered out the budget in closed-door sessions with limited, if any, input from Republican leaders. "Talk is cheap," said Horner. "Reality is hard." Crafting a Budget New York State's budget process in kicked off when the governor introduces a budget proposal in January. The legislature's financial committees then hold hearings to review the soundness of the governor's plan. According to the New York State Department of Budget Web site, "the legislature, primarily through its fiscal committees -- Senate Finance and Assembly Ways and Means -- analyzes the governor's spending proposals and revenue estimates, holds public hearings on major programs, and seeks further information from the Division of the Budget and other state agencies." In most years, both houses of the legislature would pass separate budget bills, and then, since 2007, they would hold conference committees to discuss differences between their separate budget bills -- an attempt to clarify the process. "Under budget reform legislation passed in 2007, the legislature is required to use a conference committee process between the two houses to organize its deliberations, set priorities and reach agreement on a budget," the Division of Budget Web site says. The legislature held hearings on Paterson's proposed budget earlier this year, but so far the leaders have chosen not to hold another round of conference committees. The Quiet Before the Storm No one doubts the state faces a dire budget situation. Up until the last minute, though, it was hard to detect that from the scene in the Capitol. Last week, normally talkative Democrats scuttled away from reporters who had questions about the budget on their lips. Near the Senate chamber Sen. Eric Schneiderman blurted to a reporter, "What do you want from me?" The reporter shot back, "I want answers!" In all fairness, Schneiderman might not have had the answers since the three men in the room stingily parceled out information. As the negotiations dragged on, legislators who were told about parts of the deal dished out tidbits on what they thought might be in place but warned that things were steadily shifting. Legislative action in the Senate slowed to a crawl in recent weeks as the focus shifted to the budget deal. The Senate spent the last few weeks honoring citizens and commending the recently deceased rather than passing substantive bills. Senate Majority Leader Malcolm Smith, when asked about serious pieces of legislation, repeatedly said they will be addressed "after the budget." The Assembly, thanks to a Democratic supermajority, moved quickly on again approving bills that it had passed in previous years, bills addressing issues like Rockefeller Drug Law reform and rent control. However, the members hesitated to consider new legislation knowing that their action would be futile without support from the Senate. Silver did not act to pass his compromise plan to address the Metropolitan Transportation Authority's financial straits, nor did his house vote on an income tax increase for the wealthy, a measure that is now in the budget bill. Hopes for Transparency Advocates of open government initially thought they had allies in the Democratic leadership. Paterson, for example, had made a number of comments about his commitment to ending the secretive budget practices, which long plagued Albany. Advocates had solidified relationships with the new majority after years when Senate Democrats -- then in the minority -- struggled to gain a seat at the table and to have their input taken seriously. At the same time, good government groups pushed to make the budget process more open. Much, though, has changed since then -- as evidenced in the Democrat's new attitude toward the budget conference committees. The 2007 law that created the committees was passed when the Republicans controlled the Senate and Democrats controlled the Assembly. And Silver signed on. In a 2007 press release now being distributed by Republicans, the speaker said that conference committees would "move our state's budget process in the 21st century with a strong constitutional emphasis on mutual respect between the executive and legislative branches in forging a fiscal plan for our state. We will continue to rely upon the joint conference committees. We will have a more transparent, more easily understood budget process." This year, with Democrats controlling both houses, Silver said there is no need for conference committees. "We're all Democrats," he said. "We're not going to have big philosophical differences." Republican Minority leader Dean Skelos has said that not holding conference committees is illegal. But Silver has repeatedly declared that, if there are no differences between the budget bills in the two houses, there is nothing to be discussed in conference committees. In fact, Silver has said, there might not even be separate Assembly and Senate budget bills. For his part, Smith repeatedly insisted that he would hold conference committees. But as of Sunday night, with the budget apparently all but certain, that had not happened. Those who observed conference committees in previous years point out that they were heavily scripted and did not actually produce more open government. Legislators would use the meetings to give speeches and hold their substantive discussions in private. By doing away with the committees and one-house budget bills, however, Silver is admitting that they were only window dressing on an ugly budget process -- just another way to placate the public. Barbara Bartoletti of the League of Women Voters noted that the legislature fought to amend the budget process under Gov. George Pataki because he kept the budget process notoriously secretive. "It was known as Fort Pataki," she said. According to Bartoletti, Gov. Eliot Spitzer made it a priority to open up the process and now Paterson, Smith and Silver are disregarding that work. "This is a blatant violation of the law they passed in 2007!" said Bartoletti. "If regular people violate the law they get in trouble, but apparently these guys think they are above the law." At a briefing Friday, reporters asked Paterson about the lack of transparency in the budget process. "I think there should be transparency in terms of the process and openness in terms of government," Paterson responded. "However, when you are in a budget position, it is very hard to negotiate in public. You never see President Obama and Senator Reid and Speaker Pelosi do it. You don't see it in any other state." And Paterson continued, "You don't see it in labor negotiations and I dare say that your negotiations with your own media outlet, your contract, is not, the last I checked, publicly observed." Paterson failed to mention that his salary is paid by the taxpayers and reporters' salaries are not. "There comes a point in the negotiations," continued Paterson, "where anyone who is really negotiating has to take things off the table. This is a very difficult endeavor, and it's hard to do it when the advocates you are fighting for are right there." New Leaders, Old Habits Silver, of course, is the only leader remaining from 2007. This year's budget negotiations took place with two new leaders -- Paterson and Smith, both of whom are considered weak and vulnerable. Smith has been rendered powerless by the combination of a slim majority and indecisive behavior. Paterson, thanks to plummeting poll numbers and his own brand of indecision is seen by many as nearly "irrelevant." Smith and Paterson apparently hope that an on-time budget, no matter what it contains -- or how it's drafted -- will make them look responsible to the public and give them a political boost. In addition, the lack of transparency might have helped Smith move things into the budget that would be controversial to some members. His majority is so slim that he can't afford "no" votes from any Democrats. That is why instead of passing legislation on drug law reform Smith has included it as part of the budget negotiations. "The thinking on this issue is that there is an explicit rush to get this through," said Robert Gangi, the executive director of the Correctional Association of New York State. They wanted to have it included as part of the budget so that neither side can cherry pick. They have to vote up or down for the whole kit and caboodle." The three announced they had reached a deal on drug reforms on Friday but did not offer a detailed account of what was agreed on. Health care advocates have spent the last week using advertisements to target individual legislators and alert citizens about what they think will be tremendous cuts to health care funding and Medicaid payments to hospitals. William Van Slyke from the Healthcare Association of New York, which represents health care networks and hospitals, thinks it is important to make sure legislators and voters know exactly what kinds of cuts are being considered. But he said last week, "Rank and file legislators don't even know what is in the budget. The Senate is in disarray." For a week, information about "tentative" deals made its way around the Capitol before quickly being denounced or refuted by one of the three men in the room. Silver flatly denied a New York Times report that a deal on drug law reform had been reached, only to hold a meeting to announce the deal the next morning. There was talk that a deal had been reached to institute the Bigger Better Bottle Bill, which would have put a deposit fee on noncarbonated beverages like water and tea and made beverage companies give the state unclaimed deposits. But it was reported quickly thereafter that the tentative deal had fallen apart. The bill is now back in as part of the budget deal, but only with deposits on water -- not juice or tea. Bartoletti said there are many advantages for the three men in a room to keep the deal hush-hush as long as they possibly can. "Special interests still run Albany. It was probably lobbying or campaign contributions that killed the bottle deal but we won't know for two months till we see the contributions," she said before word came that parts of the bottle bill were back in. "It is the same thing with healthcare: We don't know because it is behind closed doors and special interests have their influence." According to Horner, the budget crunch provides another convenient excuse to do business in secret. "This is unlike any other year," he said. "Thanks to the federal stimulus, the budget the governor presented is being entirely reworked, and it is being reworked behind closed doors." "They are going to get away with it this year," said Bartoletti. "They think the public has a short memory and they will say they did it because of the financial crisis. They will even come out and say this was a bad process this year but we had to do it and we will do it better next year." Opaque Government Bartoletti describes this year's budget process as a "drive-by negotiation," because legislators driving away from leaders' meetings at the governor's mansion sometimes had the decency to pause briefly to give reporters placating, dismissive answers about what was discussed -- or, in the case of Republican leaders, to complain about how little input they actually have. Last Tuesday, March 24, Republican legislators and open government groups stood together in the same room to call for Democrats to make the process more open. Skelos said he had not been invited to attend the "secret leaders meeting" that was going on just one floor below among the three Democratic leaders. He said he thought Democrats would probably rush the budget through by issuing a so-called "message of necessity" that would eliminate the three-day waiting period normally required before the legislature votes on a bill. This would ensure, of course, that even fewer senators and Assembly members would have any idea about what's in the spending plan. "Under the guise of getting a budget done on time, Governor Paterson, Senator Smith and Speaker Silver are prepared to rush through a budget in the dead of night with no time for public input or examination," said Skelos in a written statement. Bartoletti expected that "legislators won't see the budget until 15 minutes before they vote and no one will even know what's in it." It was not quite that dire: Legislators will have part of the weekend and two days to review the bills. And, of course, getting bills on short notice is nothing unusual in Albany. Longtime Democratic Sen. Neil Breslin said he has "gotten bills two minutes before" he voted on them. Last Tuesday, Smith canceled a number of public appearances to attend "budget negotiations." Meanwhile, the three leaders released a statement saying the budget deficit had increased by $2 billion to $16 billion. Republicans said the announcement was just cover for an impending announcement of a tax increase. Then news broke that Paterson had ordered the layoff of 8,900 state workers. The big three were nowhere to be seen. At 3 p.m., school children in white shirts observed a poorly attended session of the Senate. The Senate asked the children to stand to be recognized, and then the few legislators in attendance voted to honor a recently deceased labor leader and tabled legislation pertaining to warning lights on bicycles. When the end of the session was called, a young girl looked up incredulously and said, "We came all the way for this? That's it?" Comments Comment(s) The comments section is provided as a free service to our readers. Gotham Gazette's editors reserve the right to delete any comments. Some reasons why comments might get deleted: inappropriate or offensive content, off-topic remarks or spam. Last Updated (May 22, 2013) Donate now Subscribe To Our Daily Newsletter The Eye-Opener First Last Email Or Manage Most popular Letting the Sun In: The State of New York Government Transparency The Mayor's Vacant Lots What’s Next for East Midtown De Blasio's Homelessness Reset: Advantage Lessons Learned Expanding de Blasio’s Agenda for Youth Opportunities Tweets by @GothamGazette Gotham Gazette The Place for New York Policy and politics Follow @twitterapi About Us Contact Us Advertise Newsletters Write For Us Career Gotham Gazette is published by Citizens Union Foundation and is made possible by support from the Robert Sterling Clark Foundation, the John S. and James L. Knight Foundation, the Altman Foundation,the Fund for the City of New York and donors to Citizens Union Foundation. Please consider supporting Citizens Union Foundation's public education programs. Critical early support to Gotham Gazette was provided by the Charles H. 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Analysis: Remedies beyond the pay freeze By Howard Risher House Panel: No Pay Raises for Congress in 2015 April 9, 2014 The Incredible Shrinking Pay Raise in One Chart Union Calls Obama’s Proposed 1 Percent Raise ‘Pitiful’ Two years? Three years? Complete freeze? Partial freeze? It seems certain that pay for federal employees will be frozen in some form. It also appears that their retirement benefits will be reduced. The final recommendations of President Obama's fiscal commission released on Dec. 1 would bring federal benefit plans more in line with common private sector practices. The savings clearly are important, but the impact on government operations in 2011 could be far greater than analysts expect. Almost 500,000 federal employees were eligible to retire in 2009. If the commission's recommendations are adopted for 2012, that could be an incentive for many to retire next year. A switch to the high five will reduce vested benefits as well, so that many more could opt to leave as soon as they can. The freeze also will inhibit federal hiring and trigger attrition. Resignations among young new hires, already a concern, are likely to increase as the economy improves and private sector alternatives rise. Perhaps more important is the image of government as a career path will be damaged. Indeed, the federal pay debate already has denigrated the value of federal workers. There are questions about the comparisons of federal and nonfederal jobs and salaries. It is indisputable that federal salaries for new college graduates already are low, however. The national average this year is $48,351 as compared with the General Schedule Grade 7 pay of $42,209 in Washington. For high-tech grads -- engineers and computer specialists -- the averages are around $60,000. That gap risks damaging future government operations -- and it's going to widen with the freeze. Time to Assess Facts Because a freeze will not alter the comparison between federal and nonfederal salaries, the debate will continue. The Office of Personnel Management claims federal employees are badly underpaid, while the Cato Institute and the Heritage Foundation say they are overpaid. So far, both sides have based their arguments on arcane statistical analyses. The debators on both sides bear a striking resemblance to the ministers in the tale The Emperor's New Clothes. Up to this point, neither side has generated information showing how much federal employees should be paid. The duration of the two-year freeze coincides with the run-up to the 2012 election. The period would be an ideal time to develop credible market pay data and give leaders the opportunity to evaluate the facts. It would be advantageous to agree on the facts so that federal pay does not become a contentious issue in the election campaign. Neither side currently relies on a data source, or on analytical methods suited to salary planning. The analyses each used are based on government data that was collected for other purposes. Cato relied on Bureau of Economic Analysis data while Heritage used the Current Population Survey database. OPM and the Federal Salary Council rely on Bureau of Labor Statistics data. So regardless of how the data are analyzed, results are not comparable. Actually, no employer determining salaries uses a methodology remotely similar to the Salary Council's or that used by either Cato or Heritage. Other employers would not consider using those data sources. The universal approach used by corporations, hospitals, universities, and even many mom-and-pop businesses is to obtain information on what other employers are paying in the relevant labor market(s) for similar jobs. Their logic is simple. There are an estimated 2,000-plus surveys conducted annually that report pay for benchmark jobs. There are also a growing number of Internet data sources. Data are available showing pay levels for a long list of occupations. The surveys report salary levels, job by job, using simple, descriptive statistics -- means, medians and percentiles. Data from several surveys are commonly combined to determine market pay levels, but anyone opening a survey report would be able to interpret them. To be sure, salary surveys can be poorly executed and misused. Some are garbage in, garbage out. But there are good ones. In the Washington area, for example, the survey a local human resources association conducted has a broad cross-section of 340 local employers and data for more than 80,000 job incumbents -- a database far larger database than the BLS National Compensation Survey. OPM some years ago matched federal jobs to the benchmarks in the local survey. There are similar surveys done around the country. A few weeks ago The Washington Post reported a poll showing a solid 75 percent of respondents agreeing that "federal agencies should offer pay and benefits that are about the same as those provided in comparable private sector jobs." That could be the basis for a policy that would be broadly accepted. The Problem Is the General Schedule All the parties are on record agreeing that the General Schedule should be replaced with one more market-sensitive. But market concerns are only the tip of the iceberg. The roots of the job classification system can be traced back a century. It is difficult to imagine any practice more bureaucratic and less conducive to smart utilization of employee capabilities. Step increases are another concern. Pay for performance is effectively universal for white-collar jobs in virtually every other sector. In the academic world, even the critics of performance pay get rewarded in some way for their performance. OPM in 2002 published a white paper that remains the most extensive discussion of the reasons a new salary system is needed. OPM Director John Berry voiced basic agreement with the white paper in a speech late last year. Heritage analyst James Sherk said, "Uncle Sam should move to performance-based pay based on market rates -- the same system most private employers use." The same recommendation is made in the OPM white paper, at least three reports by the National Academy of Public Administration, and two of the many reports generated over the years under the leadership of former Federal Reserve chairman Paul Volcker. A few weeks ago the Partnership for Public Service published a report, Closing the Gap: Seven Obstacles to a First-Class Federal Workforce, summarizing the views of agency chief human capital officers. The officers were asked to say what it would take to bring about change, further strengthen the civil service and improve government operations. Most replies focused on hiring reform, but the second-most cited obstacle was "an antiquated and overly rigid pay and classification system." Proponents of pay for performance were dealt a setback by the Defense Department's experience with the National Security Personnel System and the Defense Civilian Intelligence Personnel System, along with the subsequent decision to revert to the GS system. The trend to move away from rigid, tenure-based systems continues, however, both here and in other countries. Significantly, the teams that evaluated NSPS and DCIPS found problems, but concluded both systems could and should be salvaged. There is a long list of successful alternative demonstration projects and Title 5-exempt agencies with separate salary systems. This winter would be an ideal time to assess that experience to understand what worked and what didn't. The evaluation of DCIPS that NAPA conducted is a good prototype. Federal leaders should use it to avoid mistakes and to build on proven practices. Their conclusions then should be used to plan a replacement for the GS system. The basic program model -- a framework based on salary bands -- has been used in some places for 30 years. The lessons learned from that experience will facilitate the drafting of new policies and procedures to manage salaries. Such a project is very doable during the next two years. The GS system must be replaced. Agencies need a reward system that supports mission accomplishment. The country would not be well-served by allowing this debate to continue into 2013. Howard Risher is an independent compensation and performance management consultant. He was the managing consultant for the studies leading to the 1990 Federal Employees Pay Comparability Act. He has a doctorate in labor and economics from the Wharton School at the University of Pennsylvania.

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82 Stat. 445 - An Act to amend the Act prohibiting fishing in the territorial waters of the United States and in certain other areas by vessels other than vessels of the United States and by persons in charge of such vessels Dates in SessionBegun on Monday, January 15, 1968 adjourned sine die on Monday, October 14, 1968 Page445 Date ApprovedJuly 26, 1968 Full TitleAn Act to amend the Act prohibiting fishing in the territorial waters of the United States and in certain other areas by vessels other than vessels of the United States and by persons in charge of such vessels Associated Bill NumberS. 1752 Table of Contents, List of Bills Enacted into Public and Private Laws, List of Public and Private Laws, List of Reorganization Plans, List of Concurrent Resolutions, and List of Proclamations Public Law 90-250 - Joint resolution extending the dates for transmission of the Economic Report and the report of the Joint Economic Committee Public Law 90-251 - An Act to amend the Presidential Inaugural Ceremonies Act Public Law 90-252 - An Act to increase the amounts authorized for Indian adult vocational education Public Law 90-253 - Joint resolution authorizing the President to proclaim the period February 11 through 17, 1968, as ""LULAC Week"" Public Law 90-254 - An Act to authorize the Secretary of the Interior to engage in feasibility investigations of certain water resource developments, and for other purposes Public Law 90-255 - An Act to amend section 408 of the National Housing Act, as amended, to provide for the regulation of savings and loan holding companies and subsidiary companies PDF | More Public Law 90-256 - An Act to determine the rights and interests of the Navajo Tribe and the Ute Mountain Tribe of the Ute Mountain Reservation in and to certain lands in the State of New Mexico, and for other purposes PDF | More Public Law 90-257 - An Act to amend the Railroad Retirement Act of 1937 and the Railroad Unemployment Insurance Act to provide for increase in benefits, and for other purposes Public Law 90-258 - An Act to amend the Commodity Exchange Act, as amended Public Law 90-259 - An Act to amend the Organic Act of the National Bureau of Standards to authorize a fire research and safety program, and for other purposes Public Law 90-260 - An Act to provide for credit to the Kings River Water Association and others for excess payments for the years 1954 and 1955 Public Law 90-261 - An Act to amend section 2 of the Migratory Bird Conservation Act Public Law 90-262 - An Act to authorize an exchange of lands at Acadia National Park, Maine Public Law 90-263 - An Act to provide that a judgment or decree of the United States District Court for the District of Columbia shall not constitute a lien until filed and recorded in the office of the Recorder of Deeds of the District of Columbia, and for other purposes Public Law 90-264 - An Act to supplement the purposes of the Public Buildings Act of 1959 (73 Stat. 479), by authorizing agreements and leases with respect to certain properties in the District of Columbia, for the purposes of a national visitor center, and for other purposes Public Law 90-265 - An Act to authorize the Secretary o2 Agriculture to sell to the village of Central State of New Mexico, certain lands administered by him formerly part of the Fort Bayard Military Reservation, N. Mex. Public Law 90-266 - An Act to authorize the consolidation and use of funds arising from judgments in favor of the Apaclie Tribe of the Mescalero Reservation and of each of its constituent groups Public Law 90-267 - An Act to amend the Export-Import Bank Act of 1945, as amended, to change the name of the Bank, to extend for five years the period within which the Bank is authorized to exercise its functions, to increase the Bank's lending authority and its authority to issue, against fractional reserves, export credit insurance and guarantees, to restrict the financing by the Bank of certain transactions, and for other purposes Public Law 90-268 - An Act to amend the Merchant Marine Act, 1936, with respect to the development of cargo container vessels, and for other purposes Public Law 90-269 - An Act to eliminate the reserve requirements for Federal Reserve notes and for U.S. notes and Treasury notes of 1890 Public Law 90-270 - An Act to designate the Oahe Reservoir on the Missouri River in the States of North Dakota and South Dakota as Lake Oahe Public Law 90-271 - An Act to designate the San Rafael Wilderness, Los Padres National Forest, in the State of California Public Law 90-272 - Joint resolution to approve long-term contracts for delivery of water from Navajo Reservoir in the State of New Mexico, and for other purposes Public Law 90-273 - Joint resolution calling on the Boy Scouts of America to serve the youth of this Nation as required by their congressional charter Public Law 90-274 - An Act to provide improved judicial machinery for the selection of Federal juries, and for other purposes Public Law 90-275 - An Act to amend title 38 of the United States Code to liberalize the provisions relating to payment of pension, and for other purposes Public Law 90-276 - An Act to provide for the Conveyance of certain real property of the United States to the Alabama Space Science Exhibit Commission Public Law 90-277 - Joint resolution to provide for the designation of the second week of May of 1968 as ""National School Safety Patrol Week"" Public Law 90-278 - An Act to to determine the respective rights and interests of the Confederated Tribes of the Colville Reservation and the Yakima Tribes of Indians of the Yakima Reservation and their constituent tribal groups in and to a judgment fund on deposit in the Treasury of the United States, and for other purposes Public Law 90-279 - An Act to provide that the United States shall hold certain Chilocco Indian School lands at Chilocco, Okla., in trust for the Cherokee Nations upon payment by the Cherokee Nation of $3.75 per acre to the Federal Government Public Law 90-280 - An Act relating to Federal support of education of Indian students in sectarian institutions of higher education Public Law 90-281 - Joint resolution to proclaim National Jewish Hospital Save Your Breath Month Public Law 90-282 - An Act to establish the Saugus Iron Works National Historic Site in the State of Massachusetts, and for other purposes Public Law 90-283 - An Act to amend the National Traffic and Motor Vehicle Safety Act of 1966 relating to the applications of certain standards to motor vehicles produced in quantities of less than five hundred Public Law 90-284 - An Act to prescribe penalties for certain acts of violence or intimidation, and for other purposes Public Law 90-285 - Joint resolution to continue for a temporary period the 7 percent excise tax rate on automobiles and the 10 percent excise tax rate on communication services Public Law 90-286 - Joint resolution making a supplemental appropriation for the fiscal year ending June 30, 1968, and for other purposes Public Law 90-287 - An Act relating to the Tiwa Indians of Texas Public Law 90-288 - An Act to prohibit unfair trade practices affecting producers of agricultural products, and for other purposes Public Law 90-289 - An Act to authorize appropriations to the Atomic Energy Commission in accordance with section 261 of the Atomic Energy Act of 1954, as amended, and for other purposes Public Law 90-290 - An Act to amend the District of Columbia Uniform Gifts to Minors Act to provide that gifts to minors made under such act may be deposited in savings and loan associations and related institutions, and for other purposes Public Law 90-291 - An Act to provide certain benefits for law enforcement, officers not employed by the United States who are killed or injured while apprehending violators of Federal law Public Law 90-292 - An Act to amend the act of June 20, 1906, and the District of Columbia election law to provide for the election of members of the Board of Education of the District of Columbia Public Law 90-293 - An Act to grant the masters of certain U.S. vessels a lien on those vessels for their wages Public Law 90-294 - An Act to amend the Communications Act of 1934 by extending the authorization of appropriations for the Corporation for Public Broadcasting. Public Law 90-295 - An Act for the relief of the city of El Dorado, Kansas Public Law 90-296 - An Act to provide for the temporary transfer to a single district for coordinated or consolidated pretrial proceedings of civil actions pending in different districts which involve one or more common questions of fact, and for other purposes Public Law 90-297 - An Act to authorize appropriations for the saline water conversion program for fiscal year 1969, and for other purposes. Public Law 90-298 - An Act to amend provisions of the Shipping Act, 1916, to authorize the Federal Maritime Commission to permit a carrier to refund a portion of the freight charges Public Law 90-299 - An Act to amend Communications Act of 1934 with respect to obscene or harassing telephone calls in interstate or foreign commerce Public Law 90-300 - An Act to amend section 14(b) of the Federal Reserve Act, as amended, to extend for 2 years the authority of Federal Reserve banks to purchase U.S. obligations directly from the Treasury Public Law 90-301 - An Act to amend title 38 of the United States Code so as to increase the amount of home loan guaranty entitlement from 7,500 to $10,000, and for other purposes Public Law 90-302 - An Act to amend the National School Lunch Act to strengthen and expand food service programs for children, and for other purposes Public Law 90-303 - An Act to provide for the striking of medals in commemoration of the one hundredth anniversary of the compIetion of the first transcontinental railroad Public Law 90-304 - An Act to amend the acts of February 1, 1826, and February 20, 1833, to authorize the State of Ohio to use the proceeds from the sale of certain lands for educational purposes Public Law 90-305 - Joint resolution to designate May 20, 1968, as ""Charlotte, North Carolina, Day"" Public Law 90-306 - An Act to amend the Act of March 1, 1933 (47 Stat. 1418), entitled ""An Act to permanently set aside certain lands in Utah as an addition to the Navajo Indian Reservation, and for other purposes"" Public Law 90-307 - An Act to direct the Secretary of Agriculture to release on behalf of the United States conditions in a deed conveying certain lands to the University of Maine and to provide for conveyance of certain interests in such lands so as to permit such university, subject to certain conditions, to sell, lease, or otherwise dispose of such lands Public Law 90-308 - An Act to grant minerals, including oil and gas, on certain lands in the Crow Indian Reservation, Montana. to certain Indians, and for other purposes. Public Law 90-309 - An Act to provide for the observance of the centennial of the signing of the 1868 Treaty of peace between the Xavajo Indian Tribe and the United States. Public Law 90-310 - An Act to authorize the Secretary of the Army to quit-claim certain real property in Muscogee County, Georgia. Public Law 90-311 - An Act to amend the repayment contract with the Foss Reservoir Master Conservancy District, and for other purposes Public Law 90-312 - An Act to declare a portion of Boston Inner Harbor and Fort Point Channel nonnavigable Public Law 90-313 - Joint resolution to authorize the Secretary of Transportation to conduct a comprehensive study and investigation of the existing compensation system for motor vehicle accident losses, and for other purposes Public Law 90-314 - An Act to amend the Arms Control and Disarmament Act, as amended, in order to extend the authorization for appropriations Public Law 90-315 - An Act to increase the authorization for appropriation for continuing work in the Missouri River Basin by the Secretary of the Interior. Public Law 90-316 - Joint resolution to provide for the issuance of a gold medal to the widow of the late Walt Disney and for the issuance of bronze medals to the California Institute of the Arts in recognition of the distinguished public service and the outstanding contributions of Walt Disney to the United States and to the world Public Law 90-317 - An Act to place in trust statns certain lands on the Wind River Indian Reservation in Wyoming Public Law 90-318 - An Act to designate the San Gabriel Wilderness, Angeles National Forest, in the State of California Public Law 90-319 - An Act to amend the District of Columbia Teachers Salary Act of 1955 to provide salary increases for teachers and school officers in the District al Columbia public schools, and for other purposes Public Law 90-320 - An Act to amend the District of Columbia Police and Firemen's Salary Act of 1958 to increase salaries, and for other purposes Public Law 90-321 - An Act to safeguard the consumer in connection with the utilization of credit by requiring full disclosure of the terms and conditions of finance charges in credit transactions or in offers to extend credit; by restricting the garnishment of wages; and by creating the National Commission on Consumer Finance to study and make recommendations on the need for further regulation of the consumer finance industry; and for other purposes Public Law 90-322 - Joint resolution to provide for the reappointment of Doctor Crawford H. Greenewalt as Citizen Regent of the Board of Regents of the Smithsonian Institution Public Law 90-323 - Joint resolution to provide for the reappointment of Doctor Caryl P. Haskins as Citizen Regent of the Board of Regents of the Smithsonian Institution Public Law 90-324 - Joint resolution to provide for the reappointment of Doctor William A. M. Burden as Citizen Regent of the Board of Regents of the Smithsonian Institution Public Law 90-325 - An Act to provide for increased participation by the United States in the Inter-American Development Bank, and for other purposes Public Law 90-326 - An Act to authorize the appropriation of funds for Cajp Hatteras National Seashore Public Law 90-327 - An Act to authorize the Secretary of Agriculture to establish the Robert S. Kerr Memorial Arboretum and Nature Center in the Ouachita National Forest in Oklahoma, and for other purposes Public Law 90-328 - Joint resolution to authorize the temporary funding of the Emergency Credit Revolving Fund Public Law 90-329 - An Act to amend title 10, United States Code, to change the name of the Army Medical Service to the Army Medical Department Public Law 90-330 - An Act to amend section 703(b) of title 10, United States Code, to make permanent the authority to grant a special 30-day period of leave for members of the uniformed services who voluntarily extend their tours of duty in hostile fire areas Public Law 90-331 - Joint resolution to authorize the United States Secret Service to furnish protection to major presidential or vice presidential candidates Public Law 90-332 - An Act to amend Public Law 90-60 with respect to judgment funds of the Ute Mountain Tribe Public Law 90-333 - An Act to amend the Act of February 14, 1931, relating to the acceptance of gifts for the benefits of Indians Public Law 90-334 - An Act to authorize appropriations for procurement of vessels and aircraft and construction of shore and offshore establishments for the Coast Guard Public Law 90-335 - An Act to authorize the purchase, sale, and exchange of certain lands on the Spokane Indian Reservation, and for other purposes Public Law 90-336 - An Act to further amend the Federal Civil Defense Act of 1950, as amended, to extend the expiration date of certain authorities thereunder, and for other purposes Public Law 90-337 - An Act to authorize the use of funds arising from a judgment in favor of the Spokane Tribe of Indians. Public Law 90-338 - Joint resolution authorizing the National Commission on the Causes and Prevention of Violence to compel the attendance and testimony of witnesses and the production of evidence Public Law 90-339 - An Act to provide for the adjustment of the legislative jurisdiction exercised by the United States over lands within the Crab Orchard National Wildlife Refuge in Illinois Public Law 90-340 - An Act to amend section 867(a) of title 10, United States Code, in order to establish the Court of Military Appeals as the United States Court of Military Appeals under article I of the Constitution of the United States, and for other purposes PDF | More Public Law 90-341 - An Act to change the provision with respect to the maximum rate of interest permitted on loans and mortgages insured under title XI of the Merchant Marine Act, 1936. Public Law 90-342 - Joint resolution to authorize the President to reappoint as Chairman of the Joint Chiefs of Staff, for an additional term of one year, the officer serving in that position on April 1, 1968 PDF | More Public Law 90-343 - An Act to amend the Federal Voting Assistance Act of 1955 so as to recommend to the several States that its absentee registration and voting procedures be extended to all citizens temporarily residing abroad. Public Law 90-344 - An Act to amend the Federal Voting Assistance Act of 1955 (69 Stat. 584) Public Law 90-345 - An Act to amend the Federal Farm LoAn Act and the Farm Credit Act of 1933, as amended, to improve the capitalization of Federal intermediate credit banks and production credit associations, and for other purposes Public Law 90-346 - An Act to amend the Internal Revenue Code of 1954 with respect to advertising in a convention program of a national political convention Public Law 90-347 - An Act to provide for the appointment of additional circuit judges Public Law 90-348 - An Act to amend the National Foundation on the Arts and the Humanities Act of 1965 Public Law 90-349 - An Act to provide for United States participation in the facility based on Special Drawing Rights in the International Monetary Fund, and for other purposes Public Law 90-350 - An Act making appropriations for the Treasury and Post Office Departments, the Executive Office of the President, and certain independent agencies, for the fiscal year ending June 30, 1969, and for other purposes Public Law 90-351 - An Act to assist State and local governments in reducing the incidence of crime, to increase the effectiveness, fairness, and coordination of law enforcement and criminal justice systems at all levels of government, and for other purposes Public Law 90-352 - Joint resolution making supplemental appropriations for the fiscal year ending June 30, 1968, and for other purposes Public Law 90-353 - An Act to permit black and white or color reproductions of U.S. and foreign postage stamps under certain circumstances, and for other purposes Public Law 90-354 - An Act to amend the District of Columbia Public Education Act Public Law 90-355 - An Act to amend the act of August 9, 1955, to authorize longer term leases of Indian lands on the Hualapai Reservation in Arizona Public Law 90-356 - An Act for the relief of Barney Elrod Construction Co., Inc (For the relief of Gilmer County, Georgia) Public Law 90-357 - An Act to correct and improve the Canal Zone Code, and for other purposes Public Law 90-358 - An Act to remove certain limitations on ocean cruises Public Law 90-359 - An Act to amend sections 3 and 4 of the act approved September 22, 1964 (78 Stat. 990), providing for an investigation and study to determine a site for the construction of a sea-level canal connecting the Atlantic and Pacific Oceans. Public Law 90-360 - An Act to authorize the Secretary of Agriculture to convey certain lands to the city of Glendale, Arizona Public Law 90-361 - An Act to amend the Watershed Protection and Flood Prevention Act to permit the Secretary of Agriculture to contract for the construction of works of improvement upon request of local organizations Public Law 90-362 - An Act to authorize the further amendment of the Peace Corps Act. Public Law 90-363 - An Act to provide for uniform annual observances of certain legal public holidays on Mondays, and for other purposes Public Law 90-364 - An Act to continue the existing excise tax rates on communication services and on automobiles, and to apply more generally the provisions relating to payments of estimated tax by corporations Public Law 90-365 - An Act to permit Federal employees to purchase shares of Federal- or State-chartered credit unions through voluntary payroll allotments Public Law 90-366 - Joint resolution making supplemental appropriations for the fiscal year 1969, and for other purposes Public Law 90-367 - An Act to amend title 5, United States Code, to extend certain benefits to former employees of county committees established pursuant to section 8(b) of the Soil Conservation and Domes.tic Allotment Act, and for other purposes PDF | More Public Law 90-368 - Joint resolution to provide franked mail privileges for surviving spouses of Members of Congress Public Law 90-369 - An Act to provide for the expeditious naturalization of the surviving spouse of a U.S. citizen who dies while serving in An Active duty status in the Armed Forces of the United States Public Law 90-370 - An Act to amend the Defense Production Act of 1950, and for other purposes Public Law 90-371 - An Act to authorize the Bureau of Prisons to assist State and local governments in the improvement of their correctional systems Public Law 90-372 - An Act to designate the U.S. Customs House Building in Providence, R.I., as the ""John E. Fogarty Building"". Public Law 90-373 - An Act to authorize appropriations to the National Aeronautics and Space Administration for research and development, construction of facilities, and administrative operations, and for other purposes Public Law 90-374 - An Act to amend title 10, United States Code, to increase the number of congressional alternates authorized to be nominated for each vacancy at the Military, Naval, and Air Force Academies Public Law 90-375 - An Act to amend the Federal Credit Union Act Public Law 90-376 - An Act authorizing the Trustees of the National Gallery of Art to construct a building or buildings on the site bounded by Fourth Street, Pennsylvania Avenue, Third Street, and Madison Drive NW., in the District of Columbia, and making provision for the maintenance thereof. Public Law 90-377 - An Act to amend titles 10, 14, and 37, United States Code, to provide for confinement and treatment of offenders against the Uniform Code of Military Justice Public Law 90-378 - An Act to amend section 8306 of title 10, United States Code, to authorize certain contracts for services and related supplies to extend beyond 1 year Public Law 90-379 - An Act to amend the Communications Act of 1934, as amended, to give the Federal Communications Commission authority to prescribe regulations for the manufacture, import, sale, shipment, or use of devices which cause harmful interference to radio reception Public Law 90-380 - An Act to amend section 11-341(b) of the District of Columbia Code which relates to the sales price for the reports of the opinions of the U.S. Court of Appeals for the District of Columbia circuit Public Law 90-381 - An Act to prohibit desecration of the flag and for other purposes Public Law 90-382 - An Act to amend the act of April 3, 1952 Public Law 90-383 - An Act to amend section 127 of title 28, United States Code, to define more precisely the territory included in the two judicial districts of Virginia Public Law 90-384 - An Act to repeal section 1727 of title 18, United States Code, so as to permit prosecution of postal employees for failure to remit postage due collections, under the postal embezzlement statute, section 1711 of title 18, United States Code Public Law 90-385 - An Act to increase the limitation on the number of officers for the Coast Guard Public Law 90-386 - An Act to amend title 10, United States Code, to authorize an increase in the numbers of officers of the Navy designated for engineering duty, aeronautical engineering duty, and special duty Public Law 90-387 - An Act to amend the tobacco marketing quota provisions of the Agricultural Adjustment Act of 1938 Public Law 90-388 - An Act to authorize the secretary of Agriculture to cooperate with the several governments of Central America in the prevention, control, and eradication of foot-and-mouth disease or other pests Public Law 90-389 - An Act to provide security measures far banks and other financial institutions Public Law 90-390 - An Act to enable the Export-Import Bank of the United States to approve extension of certain loans, guarantees, and insurance in connection with exports from the United States in order to improve the balance of payments and foster the long-term commercial interests of the United States Public Law 90-391 - An Act to amend the Vocational Rehabilitation Act to extend the authorization of grants to States for rehabilitation services, to broaden the scope of goods and services available under that act for the handicapped, and for other purposes Public Law 90-393 - An Act to amend sections 13(b) of the Acts of October 3, 1962 (76 Stat. 698, 704), and for other purposes Public Law 90-394 - An Act to amend the act of August 1, 1958, in order to prevent or minimize injury to fish and wildlife from the use of insecticides, herbicides, fungicides, and pesticides, and for other purposes Public Law 90-395 - Joint resolution granting the consent of Congress to certain additional powers conferred upon the Kansas City Area Transportation Authority by the States of Kansas and Missouri Public Law 90-396 - An Act to provide for the collection, compilation, critical evaluation, publication, and sale of standard reference data Public Law 90-397 - An Act to exempt certain vessels engaged in the fishing industry from the requirements of certain laws Public Law 90-398 - An Act to authorize the Secretary of Agriculture to establish the Cradle of Forestry in America in the Pisgah National Forest in North Carolina, and for other purposes. Public Law 90-399 - An Act to protect the public health by amending the Federal Food, Drug, and Cosmetic Act to consolidate certain provisions assuring the safety and effectiveness of new animal drugs, and for other purposes Public Law 90-400 - An Act to make certain reclamation project expenses nonreimbursable Public Law 90-401 - An Act to amend title I of the Land and Water Conservation Fund Act of 1965, and for other purposes Public Law 90-402 - An Act to provide for sale or exchange of isolated tracts of tribal lands on the Flathead Reservation, Montana Public Law 90-403 - An Act to amend the Act relating to the leasing of lands in Alaska for grazing fn order to make certain improvements in such Act Public Law 90-404 - An Act to restrict the disposition of lands acquired as part of the National Wildlife Refuge System Public Law 90-405 - Joint resolution authorizing the President to proclaim August 11,1968, as ""Family Reunion Day"" Public Law 90-406 - Joint resolution to authorize the President to issue a proclamation designating the week of October 13, 1968, as ""Salute to Eisenhower Week"". Public Law 90-407 - An Act to amend the National Science Foundation Act of 1950 to make changes and improvements in the organization and operation of the Foundation, and for other purposes Public Law 90-408 - An Act to authorize certain construction at military installations, and far other purposes Public Law 90-409 - An Act to authorize the Secretary of the Interior to grant long-term leases with respect to lands in the El Portal administrative site adjacent to Yosemite National Park, Calif., and for other purposes Public Law 90-410 - An Act to direct the Secretary of Agriculture to release on behalf of the United States conditions in deeds conveying certain lands to the state of Iowa, and for other purposes Public Law 90-411 - An Act to amend the Federal Aviation Act of 1958 to authorize aircraft noise abatement regulations, and for other purposes Public Law 90-412 - An Act authorizing the use of certain buildings in the District of Columbia for chancery purposes Public Law 90-413 - An Act to amend section 1730 of title 18, United States Code, to permit the uniform or badge of the letter-carrier branch of the postal service to be worn in theatrical, television, or motion picture productions under certain circumstances. Public Law 90-414 - Joint resolution to supplement Public Law 87-734 and Public Law 87-735 which took title to certain lands in the Lower Brule and Crow Creek Indian Reservations Public Law 90-415 - An Act to increase the size of the Board of Directors of Gallaudet College, and for other purposes Public Law 90-416 - Joint resolution extending the duration of copyright protection in certain cases Public Law 90-418 - An Act to amend the Commodity Exchange Act, as amended, to make frozen concentrated orange juice subject to the provisions of such act. Public Law 90-419 - An Act granting the consent of Congress to a Great Lakes Basin Compact, and for other purposes PDF | More Public Law 90-420 - An Act to amend the Northwest Atlantic Fisheries Act of 1950 (Public Law 81-845) Public Law 90-421 - An Act to amend the International Claims Settlement Act of 1949, as amended, to provide for the timely determination of certain claims of American nationals, and for other purposes Public Law 90-422 - An Act to extend for an additional 2 years the authorization of appropriations under the State Technical Services Act of 1965. Public Law 90-423 - An Act to extend for 1 year the not of September 30, 1965, relating to high-speed ground transportation. Public Law 90-424 - An Act to grant minerals, including oil, gas, and other natural deposits, on certain lands in the Northern Cheyenne Indian Reservation, Mont., to certain Indians, and for other purposes Public Law 90-425 - An Act making appropriations for the Department of the Interior and related agencies for the final year ending June 30, 1969, and for other purposes Public Law 90-426 - An Act to extend the expiration date of the act of September 19, 1966 Public Law 90-427 - An Act to amend the Act prohibiting fishing in the territorial waters of the United States and in certain other areas by vessels other than vessels of the United States and by persons in charge of such vessels Public Law 90-428 - An Act to make several changes in the passport laws presently in force Public Law 90-429 - An Act to amend section 620, title 38, United States Code, to authorize payment of a higher proportion of hospital costs in establishing amounts payable for nursing home care of certain veterans Public Law 90-430 - An Act to extend the period during which mounts transferred from the employment security administration account in the unemployment trust fund to State accounts may be used by the States for payment of expenses of administration Public Law 90-431 - An Act to amend title 38 of the United States Code to improve vocational rehabilitation training for service-connected veterans by authorizing pursuit of such training on a part-time basis Public Law 90-432 - An Act to amend title 38 of the United States Code in order to promote the care and treatment of veterans in State veterans homes Public Law 90-433 - An Act to amend sections 203(b) (5) and 220 of the Interstate Commerce Act, as amended, and for other purposes Public Law 90-434 - An Act to amend section 212(B) of the Merchant Marine Act, 1936, as amended, to provide for the continuation of authority to develop American-flag carriers and promote the foreign commerce of the United States through the use of mobile trade fairs Public Law 90-435 - An Act to postpone for 2 years the date on which passenger vessels operating solely on the inland rivers and waterways must comply with certain safety standards. Public Law 90-436 - An Act to extend Public Law 480, Eighty-third Congress, for 2 years, and for other purposes Public Law 90-437 - An Act to amend the Securities Exchange Act of 1934 to permit regulation of the amount of credit that may be extended and maintained with respect to securities that are not registered on a national securities exchange Public Law 90-438 - Joint resolution to amend the Securities Exchange Act of 1934 to authorize an investigationof the effect on the securities marlcets of the operation of institutional investors Public Law 90-439 - An Act to providing for full disclosure of corporate equity ownership of securities under the Securities Exchange Act of 1934 Public Law 90-440 - An Act to prevent, abate , and control air pollution in the District of Columbia, and for other purposes Public Law 90-441 - An Act to provide that the prosecution of the offenses of disorderly conduct and lewd, indecent, or obscene acts shall be conducted in the name of and for the benefit of the District of Columbia. Public Law 90-442 - An Act to amend the Foreign Service Buildings Act, 1962, to authorize additional appropriations Public Law 90-443 - Joint resolution to authorize the President to designate the week of August 4 through August 10, 1968, as ""Professional Photography Week"". Public Law 90-444 - An Act to authorize the Secretary of the Army to release certain use restrictions on a tract of land in the State of Iowa in order that such land may be used as a site for the construction of buildings or other improvements for the Iowa Law Enforcement Academy. Public Law 90-445 - An Act to assist courts, correctional systems, and community agencies to prevent, treat, and control juvenile delinquency to support research and training efforts in the prevention, treatment, and control of juvenile delinquency and for other purposes Public Law 90-446 - An Act to amend title III of the Packers and Stockyards Act of 1921, as amended Public Law 90-447 - Joint resolution making continuing appropriations for the fiscal year 1969, and for other purposes Public Law 90-448 - An Act to assist in the provision of housing for low- and moderate-income families, and to extend and amend laws relating to housing and urban development. Public Law 90-449 - An Act to amend title 39, United States Code, to provide for disciplinary action against employees in the postal field service who assault other employees in such service in the performance of official duties, and for other purposes Public Law 90-450 - An Act to provide additional revenue for the District of Columbia, and for other purposes Public Law 90-451 - An Act to amend part I of the Federal Power Act to clarify the manner in which the licensing authority of the Commission and the right of the United States to take over a project or projects upon or after the expiration of any license shall be exercised Public Law 90-452 - An Act to provide a comprehensive program for the control of drunkenness and the prevention and treatment of alcoholism in the District of Columbia, and for other purposes Public Law 90-453 - An Act to authorize the Secretary of the Interior to construct, operate, and maintain the initial stage of the Oahe unit, James division, Missouri River Basin project, South Dakota, and for other purposes Public Law 90-454 - An Act to authorize the Secretary of the Interior in cooperation with the States to preserve, protect, develop, restore, and make accessible estuarine areas of the Nation which are valuable for sport and commercial fishing, wildlife conservation, recreation, and scenic beauty, and for other purposes Public Law 90-455 - An Act to require that contracts for construction, alteration, or repair of any public building or public work of the District of Columbia be accompanied by a performance bond protecting the District of Columbia and by an additional bond for the protection of persons furnishing material and labor, and for other purposes Public Law 90-456 - Joint resolution to designate the National Center for Biomedial Communications the Lister Hill National Center for Biomedical Communications Public Law 90-457 - An Act to authorize project grants and loans for construction and modernization of hospitals and other medical facilities in the District of Columbia Public Law 90-458 - An Act to establish a register of blind persons in the District of Columbia, to provide for the mandatory reporting of information concerning such persons, and for other purposes Public Law 90-459 - An Act to exempt from taxation certain property of the National Society of the Colonial Dames of America in the District of Columbia Public Law 90-460 - An Act to extend for 2 years certain programs providing assistance to students at institutions of higher education, to modify such programs, and to provide for planning, evaluation, and adequate lead-time in such programs Public Law 90-461 - An Act to amend section 508(f) of the Federal Property and Administrative Services Act of 1949 to extend for a period of five years the authorization to make appropriations for allocations and grants for the collection and publication of documentary sources significant to the history of the United States Public Law 90-462 - An Act to amend the act of June 19, 1968 (Public Law 351, 90th Congress). Public Law 90-463 - An Act making appropriations for the Department of Agriculture and related agencies for the fiscal year ending June 30, 1969, and for other purposes Public Law 90-464 - An Act making appropriations for the Department of Transportation for the fiscal year ending June 30, 1969, and for other purposes Public Law 90-465 - An Act to amend section 3 of the act of September 15, 1960, for the purpose of facilitating the conduct of the fish and wildlife conservation and rehabilitation program authorized by that act Public Law 90-466 - An Act to amend section 376 (a) of title 28, United States Code Public Law 90-467 - An Act to amend the Life Insurance Act of District of Columbia, approved June 19, 1934 (48 Stat. 1125) Public Law 90-468 - An Act to revise the boundaries of the Badlands National Monument in the State of South Dakota, to authorize exchanges of land mutually beneficial to the Oglala Sioux Tribe and the United States, and for other purposes Public Law 90-469 - An Act to provide for the operation of the William Langer Jewel Bearing Plant at Rolla, N. Dak., and for other purposes Public Law 90-470 - An Act making appropriations for the Departments of State, Justice, and Commerce, the Judiciary, and related agencies for the fiscal year ending June 30, 1969, and for other purposes Public Law 90-471 - An Act to authorize appropriations for certain maritime programs of the Department of Commerce Public Law 90-472 - An Act to authorize the Secretary of Commerce to make a study to determine the advantages and disadvantages of increased use of the metric system in the United States Public Law 90-474 - An Act to amend further section 27 of the Merchant Marine Act, 1920 Public Law 90-475 - An Act to authorize the Secretary of Agriculture to convey certain lands in Saline County, Ark., to the Dierks Forests, Inc., and for other purposes Public Law 90-476 - An Act to amend the act of August 25, 1959 (73 Stat. 420), pertaining to the affairs of the Choctaw Tribe of Oklahoma Public Law 90-477 - An Act to amend title II of the Marine Resources and Engineering Development Act of 1966 Public Law 90-478 - An Act to authorize the disposal of beryl ore from the national stockpile and the supplemental stockpile. Public Law 90-479 - An Act making appropriations for public works for water and power resources development, including certain civil functions administered by the Department of Defense, the Panama Canal, certain agencies of the Department of the Interior, the Atlantic-Pacific Interoceanic Canal Study Commission, the Delaware River Basin Commission, Interstate Commission on the Potomac River Basin, the Tennessee Valley Authority, the Water Resources Council, and the Atomic Energy Commission, for the fiscal year ending June 30, 1969, and for other purposes Public Law 90-480 - An Act to insure that certain buildings financed with Federal funds are so designed and constructed as to be accessible to the physically handicapped Public Law 90-481 - An Act to authorize the Secretary of Transportation to prescribe safety standards for the transportation of natural and other gas by pipeline, and for other purposes Public Law 90-482 - An Act to amend the Act of August 27, 1954, relative to the unlawful seizure of fishing vessels of the United States by foreign countries Public Law 90-484 - An Act to extend for 3 years the authority of the Secretary of Agriculture to make indemnity payments to dairy farmers for milk required to be withheld from commercial markets because it contains residues of chemicals registered and approved for use by the Federal Government. Public Law 90-485 - An Act to amend chapter 73 of title 10, United States Code, relating to the retired serviceman's family protection plan, and for other purposes Public Law 90-486 - An Act to clarify the status of National Guard technicians, and for other purposes. Public Law 90-487 - An Act to provide for U.S. standards and a national inspection system for grain, and for other purposes Public Law 90-488 - An Act to amend the Consolidated Farmers Home Administration Act of 1961, as amended, to provide for loans for enterprises to supplement farm income and for farm conversion to recreation, remove the annual ceiling on insured loans, increase the amount of unsold insured loans that may be made out of the fund, raise the aggregate annual limits on grants, establish a flexible loan interest rate, and for other purposes Public Law 90-489 - An Act to amend the Public Health Service Act to provide for the establishment of a National Eye Institute in the National Institutes of Health Public Law 90-490 - An Act to amend the Public Health Service Act to extend and improve the programs relating to the training of nursing and other health professions and allied health professions personnel, the program relating to student aid for such personnel, and the program relating to health research facilities, and for other purposes. Public Law 90-491 - An Act to amend and clarify the reemployment provision of the Universal Military Training and Service Act, and for other purposes Public Law 90-492 - An Act to clarify and otherwise amend the Poultry Products Inspection Act, to provide for cooperation with appropriate State agencies with respect to State poultry products inspection programs, and for other purposes PDF | More Public Law 90-493 - An Act to amend title 38, United States Code, to provide increases to rates of compensation for disabled veterans Public Law 90-494 - An Act to promote the foreign policy of the United States by strengthening and improving the Foreign Service personnel system of the United States Information Agency through establishment of a Foreign Service Information Officer Corps Public Law 90-495 - An Act to authorize appropriations for the fiscal years 1970 and 1971 for the construction of certain highways in accordance with title 23 of the United States Code, and for other purposes. Public Law 90-496 - An Act to provide for the popular election of the Governor of the Virgin Islands, and for other purposes Public Law 90-497 - An Act to provide for the popular election of the Governor of Guam, and for other purposes Public Law 90-498 - Joint resolution authorizing the President to proclaim annually the week including September 15 and 16 as ""National Hispanic Heritage Week"". Public Law 90-499 - Joint resolution authorizing and requesting the President to proclaim the week of November 17 through 23, 1968, as ""National Family Health Week"" Public Law 90-500 - An Act to authorize appropriations during the fiscal year 1969 for procurement of aircraft, missiles, naval vessels, and tracked combat vehicles, research, development, test, and evaluation for the Armed Forces, and to prescribe the authorized personnel strength of the Selected Reserve of each Reserve component of the Armed Forces, and for other purposes. Public Law 90-501 - An Act to authorize the Secretary of Defense to lend certain Army, Navy, and Air Force equipment and provide certain services to the Boy Scouts of America for use in the 1969 National Jamboree, and for other purposes Public Law 90-502 - An Act to amend title 10, United States Code, to correct an inequity affecting officers of the Supply Corps and Civil Engineer Corps of the Navy Public Law 90-503 - An Act to authorize the Secretary of the Interior to construct, operate, and maintain the Mountain Park reclamation project, Oklahoma, and for other purposes Public Law 90-504 - An Act to provide for the disposition of funds appropriated to pay a judgment in favor of the Greek Nation of Indians in Indian Claims Commission docket No. 21, and for other purposes Public Law 90-505 - An Act to extend for 2 years the authority for more flexible regulation of maximum rates of interest or dividends, higher reserve requirements, and open market operations in agency issues. Public Law 90-506 - An Act to provide for the disposition of funds appropriated to pay a judgment in favor of the Creek Nation of Indians in Indian Claims Commission docket No. 276, and for other purposes Public Law 90-507 - An Act to provide for preparation of a roll of persons of California Indian descent who are eligible to share in the distribution of certain judgment funds and for a referendum on the compromise settlement in consolidated dockets numbered 31, 37, 80, 80-D, and 347, Indian Claims Commission Public Law 90-508 - An Act to provide for the disposition of funds appropriated to pay a judgment in favor of the Delaware Nation of Indians in Indian Claims Commission docket No. 337, and for other purposes Public Law 90-509 - An Act to authorize the disposition by the city of Hot Springs, Ark., of certain property heretofore conveyed to the city by the United States, and for other purposes Public Law 90-510 - An Act to direct the Secretary of Defense to pay the special pay authorized under section 310 of title 37, United States Code, to certain members of the uniformed services held captive in North Korea Public Law 90-511 - An Act to amend the Act entitled ""An Act to provide for the rehabilitation of Guam, and for other purposes"", approved November 4, 1963. Public Law 90-512 - An Act to provide authority to increase the effectiveness of the ""Truth in Negotiations Act"". Public Law 90-513 - An Act making appropriations for military construction for the Department of Defense for the fiscal year ending June 30, 1969, and for other purposes Public Law 90-514 - An Act to amend the Federal Aviation Act of 1958 with respect to the definition of ""supplemental air transportation,"" and for other purposes. Public Law 90-515 - An Act to provide for a comprehensive review of national water resource problems and programs, and for other purposes Public Law 90-516 - An Act to authorize the sale of certain public lands Public Law 90-517 - An Act to direct the Secretary of Agriculture to release, on behalf of the United States, a condition in a deed conveying certain lands to the South Carolina State Commission of Forestry so as to permit such Commission, subject to a certain condition, to exchange such lands. Public Law 90-518 - An Act to amend section 1263 of title 18 of the United States Code to require that interstate shipments of intoxicating liquors be accompanied by bill of lading, or other document, showing certain information in lieu of requiring such to be marked an the package Public Law 90-519 - An Act to convey to the city of Kenai, Alaska, all interests of the United States in certain land located therein Public Law 90-520 - An Act to direct the Secretary of Agriculture to release on behalf of the United States a condition in a deed conveying certain lands to the State of Ohio, and for other purposes. Public Law 90-521 - An Act to amend section 2734 of title 10 of the United States Code to permit the use of officers of any of the services on claims commissions, and for other purposes to amend section 2734a of title 10 to authorize the use of Coast Guard appropriations for certain claims settlements arising out of Coast Guard activities and to amend section 2736 of title 10 to authorize advance payments in cases covered by sections 2733 and 2734 of title 10 and section 715 of title 32 involving military claims Public Law 90-522 - An Act to amend section 2733 of title 10, United States Codes to authorize the application of local law in determining the effect of claimants contributory negligence, to clarify the procedures for appeal from certain claims of determinations, and to limit the amount of attorney fees thereunder PDF | More Public Law 90-523 - An Act to provide for the rehabilitation of the Eklutna project, Alaska, and for other purposes Public Law 90-524 - An Act to amend the act of November 21, 1941 (55 Stat. 773), providing for the alteration, reconstruction, or relocation of certain highway and railroad bridges by the Tennessee Valley Authority Public Law 90-525 - An Act to amend section 2733 of title 10 of the United States Code, to include authority for the settlement of claims incident to the noncombat activity of the Coast Guard while it is operating as a service in the Department of the Treasury, to increase the authority which may be delegated to an officer or civilian attorney under subsection (g) of section 2733 from $1,000 to $2,500, and for other purposes Public Law 90-526 - Joint resolution to provide that it be the sense of Congress that a White House Conference on Aging be called by the President of the United States in 1971, to be planned and conducted by the Secretary of Health, Education, and Welfare, and for related purposes PDF | More Public Law 90-527 - An Act to authorize the use of funds arising from a judgment in favor of the Kiowa, Comanche, and Apache Tribes of Indians of Oklahoma, and for other purposes. Public Law 90-528 - An Act to provide for the striking of medals in commemoration of the 200th anniversary of the founding of Dartmouth College. Public Law 90-529 - An Act to provide for the disposition of judgment funds on deposit to the credit of the Quechan Tribe of the Fort Yuma Reservation, California, in Indian Claims Commission docket numbered 319, and for other purposes. Public Law 90-530 - An Act to provide for the disposition of :ands appropriated to pay a judgment in favor of the Muckleshoot Tribe of Indians in Indian Claims Commission docket numbered 98, and for other purposes. Public Law 90-531 - An Act to authorize a per capita distribution of $550 from funds arising from a judgment in favor of the Confederated Tribes of the Colville Reservation. Public Law 90-532 - An Act to designate certain lands in the Great Swamp National Wildlife Refuge, Morris County, N.J., as wilderness. Public Law 90-533 - An Act to provide for the disposition of funds appropriated to pay a judgment in favor of the Chickasaw Nation or Tribe of Oklahoma, and for other purposes Public Law 90-534 - An Act to authorize the purchase, sale, exchange, mortgage, and long-term leasing of land by the Swinomish Indian Tribal Community, and for other purposes. Public Law 90-535 - An Act to include in tlie prohibitions contained in section 2314 of title 18, United States Code, the transxwrtation with unlawful intent in interstate or foreign commerce of traveler's checks bearing forged countersignatures PDF | More Public Law 90-536 - An Act to amend the Tennessee Valley Authority Act of 1933 with respect to certain provisions applicable to condemnation proceedings Public Law 90-537 - An Act to establish a national memorial o Woodrow Wilson in the Smithsonian Institution. Public Law 90-538 - An Act to authorize preschool and early education programs for handicapped children Public Law 90-539 - An Act to amend the Central Intelligence Agency Retirement Act of 1964 for certain employees, and for other purposes Public Law 90-540 - An Act to establish the Flaming Gorge National Recreation Area in the States of Utah and Wyoming, and for other purposes Public Law 90-542 - An Act to provide for a National Wild and Scenic Rivers System, and for other purposes Public Law 90-543 - An Act to establish a national trails system, and for other purposes Public Law 90-544 - An Act to establish the North Cascades National Park and Ross Lake and Lake Chelan National Recreation Areas, to designate the Pasayten Wilderness and to modify the Glacier Peak Wilderness, in the State of Washington, and for other purposes Public Law 90-545 - An Act to establish a Redwood National Park in the State of California, and for other purposes. Public Law 90-546 - An Act to declare that the United States holds certain lands in trust for the Pawnee Indian Tribe of Oklahoma Public Law 90-547 - An Act to amend the Water Resources Planning Act to revise the authorization of appropriations for administering the provisions of the Act, and for other purposes. Public Law 90-548 - An Act to designate the Mount Jefferson Wilderness, Willamette, Deschutes, and Mount Hood National Forests, in the State of Oregon Public Law 90-549 - An Act to amend section 3 of the Act of November 2, 1966, relating to the development by the Secretary of the Interior of fish protein concentrate. Public Law 90-550 - An Act making appropriations for sundry independent executive bureaus, boards, commissions, corporations, agencies, offices, and the Department of Housing and Urban Development for the fiscal year ending June 30, 1969, and for other purposes Public Law 90-551 - An Act to extend the provisions of the Commercial Fisheries Research and Development Act of 1964. Public Law 90-552 - An Act to amend the Food Stamp Act of 1964, as amended. Public Law 90-553 - An Act to authorize the transfer, conveyance, lease, and improvement of, and construction on, certain property in the District of Columbia, for use as a headquarters site for the Organization of American States, as sites for governments of foreign countries, and for other purposes Public Law 90-554 - An Act to amend further the Foreign Assistance Act of 1961, as amended, and for other purposes Public Law 90-555 - An Act to authorize the Secretary of the Interior to accept donations of land for, and to construct, administer, and maintain an extension of the Blue Ridge Parkway in the States of North Carolina and Georgia, and for other purposes Public Law 90-556 - An Act to amend title 5, United States Code, to provide for the payment of overtime and standby pay to certain personnel employed in the Department of Transportation Public Law 90-557 - An Act making appropriations for the Departments of Labor and Health, Education, and Welfare, and related agencies, for the fiscal year ending June 30, 1969, and for other purposes Public Law 90-558 - Joint resolution recognizing the significant part which Harry S. Truman played in the creation of the United Nations Public Law 90-559 - An Act to amend the Food and Agriculture Act of 1965 Public Law 90-560 - An Act to amend title 39, United States Code, to regulate the mailing of master keys for motor vehicle ignition switches, and for other purposes Public Law 90-561 - An Act to provide for the settlement of claims against the District of Columbia by officers and employees of the District of Columbia for damage to, or loss of, personal property incident to their service, and for other purposes Public Law 90-562 - An Act to authorize the Secretary of the Interior to construct, operate, and maintain stage 1 of the Palmetto Bend reclamation project, Texas, and for other purposes Public Law 90-563 - An Act to provide funds on behalf of a grateful nation in honor of Dwight David Eisenhower, thirty-fourth President of the United States, to be used in support of construction of educational facilities at Eisenhower College, Seneca Falls, New York, as a distinguished and permanent living memorial to his life and deeds Public Law 90-564 - An Act to amend the Tariff Schedules of the United States with respect to the classification of Chinese gooseberries Public Law 90-565 - Joint resolution to correct certain references in section 4(i) of the Act entitled ""An Act to amend chapter 37 of title 38 of the United States Code with respect to the veterans' home loan program, to amend the National Housing Act with respect to interest rates on insured mortgages, and for other purposes"", approved May 7, 196S Public Law 90-566 - An Act to amend section 539 of the Act approved March 3, 1901, so as to provide notice of the enforcement of a security interest in real property in the District of Columbia to the owner of such real property and the Commissioner of the District of Columbia Public Law 90-567 - An Act to amend the act entitled ""An Act to provide for the annual inspection of all motor vehicles in the District of Columbia"" approved February 18, 1938, as amended Public Law 90-568 - An Act to extend the Act at September 7, 1957, relating to aircraft loan guarantees Public Law 90-569 - An Act to authorize the appropriation for the contribution by the United States for the support of the International Union for the Publication of Customs Tariffs Public Law 90-570 - An Act to amend the act of August 9, 1955, to authorize longer term leases of Indian lands on the pueblos of Cochiti, Fojoaque, Tesuque, and Zuni, in New Mexico Public Law 90-571 - An Act to extend until July 15, 1970, the suspension of duty on electrodes for use in producing aluminum Public Law 90-572 - An Act to amend section 502 of the Merchant Marine Act, 1936, relating to construction-differential subsidies Public Law 90-573 - An Act to authorize the Commissioner of the District of Columbia to enter into contracts for the inspection, maintenance, and repair of fixed equipment in District-owned buildings for periods not to exceed three years PDF | More Public Law 90-574 - An Act to amend the Public Health Service Act so as to extend and improve the provisions relating to regional medical programs, to extend, the authorization of grants for health of migratory agricultural workers to provide for specialized facilities for alcoholics and, narcotic addicts, and for other purposes Public Law 90-575 - An Act to amend the Higher Education Act of 1965, the National Defense Education Act of 1958, the National Vocational Student Loan Insurance Act of 1965, the Higher Education Facilities Act of 1963, and related Acts. Public Law 90-576 - An Act to amend the Vocational Education Act of 1963, and for other purposes Public Law 90-577 - An Act to achieve the fullest cooperation and coordination of activities among the levels of government in order to improve the operation of our federal system in an increasingly complex society, to imjprove the administration of grants-in-aid to the States, to permit provision of reimbursable technical services to State and local government, to establish coordinated intergovernmental policy and administration of development assistance programs, to provide for the acquisition, use, and disposition of land within urban areas by Federal agencies in conformity with local government programs, to provide for periodic congressional review of Federal grants-in-aid, and for other purposes Public Law 90-578 - An Act to abolish the office of United States commissioner, to establish in place thereof within the judicial branch of the Government the office of United States magistrate, and for other purposes Public Law 90-579 - An Act to increase the number and salaries of judges of the District of Columbia Court of General Sessions, the salaries of the District of Columbia Court of Appeals and the District of Columbia Tax Court, and for other purposes Public Law 90-581 - An Act making appropriations far Foreign Assistance and related agencies far the fiscal year ending June 30, 1969, and for other purposes Public Law 90-582 - An Act to amend the Federal Farm LoAn Act and the Farm Credit Act of 1933, as amended, to expedite retirement of Government capital from Federal Intermediate credit banks, production credit associations and banks for cooperatives, and for other purposes. Public Law 90-583 - An Act to provide for the control of noxious plants on land under the control or jurisdiction of the Federal Government Public Law 90-584 - An Act to provide for the disposition of funds appropriated to pay a judgment in favor of the Southern Paiute Nation of Indians in Indian Claims Commission dockets numbered 88, 330, and 330-A, and for other purposes. Public Law 90-585 - An Act to provide for the disposition of funds appropriated to pay judgments in favor of the Seminole Tribe of Oklahoma in dockets numbered 150 and 248 of the Indian Claims Commission, and for other purposes Public Law 90-586 - An Act to amend part III of the Interstate Commerce Act to provide for the recording of trust agreements and other evidences of equipment indebtedness of water carriers, and for other purposes PDF | More Public Law 90-587 - An Act to authorize the Commissioner of the District of Columbia to enter into and renew reciprocal agreements for police mutual aid on behalf of the District of Columbia with the local governments in the Washington metropolitan area Public Law 90-588 - An Act to amend title 5, United States Code, to provide time off from duty without loss of pay or reduction in leave for employees of executive agencies to attend and make necessary arrangements in connection with the funerals of their sons or daughters in the U.S. Armed Forces overseas who died in or as a result of armed conflict with w hostile foreign force or forces, and for other purposes Public Law 90-589 - An Act to make the proof of financial responsibility requirements of section 39 (a) of the Motor Vehicle Safety Responsibility Act of the District of Columbia inapplicable in the case of minor traffic violations involving drivers licenses and motor vehicle registration Public Law 90-590 - An Act to amend title 39, United States Code, with respect to use of the mails to obtain money or property under the false representations, and for other purposes Public Law 90-591 - An Act to provide for the exchange of certain lands in Shasta County, CA. Public Law 90-592 - An Act to authorize the establishment of the Carl Sandburg Home National Historic Site in the State of North Carolina, and for other purposes Public Law 90-593 - Joint resolution authorizing the erection of a statue of Benito Pablo Juarez on public grounds in the District of Columbia Public Law 90-594 - An Act to authorize the appropriation of funds for Padre Island National Seashore in the State of Texas, and for other purposes Public Law 90-595 - An Act to extend to savings notes the provisions of the Second Liberty Bond Act relating to the redemption of savings bonds and the payment of losses incurred in connection with such redemption Public Law 90-596 - An Act to authorize the Commissioner of the District of Columbia to fix and collect rents for the occupancy of space in, on, under, or over the streets of the District of Columbia, to authorize the closing of unused or unsafe vaults under such streets and the correction of dangerous conditions of vaults in or vault openings on public spaces, and for other purposes Public Law 90-597 - An Act to amend the act of September 21, 1959 (Public Law 86-339), relating to the Reservation of the Agua Caliente Band of Mission Indians Public Law 90-598 - An Act to authorize the Commissioner of the District of Columbia to enter into leases for the rental of, or to use or permit the use of, the space over and under streets and alleys in the District of Columbia, and for other purposes Public Law 90-599 - An Act to authorize the Secretary of the Army to convey to the port of Cascade Locks, Oreg., a certain interest in lands in the State of Oregon for municipal purposes. Public Law 90-600 - An Act to provide for the striking of medals in commemoration of the 150th anniversary of the founding of the city of Memphis Public Law 90-601 - An Act to promote the economic development of Guam Public Law 90-602 - An Act to amend the Public Health Service Act to provide for the protection of the public health from radiation emissions from electronic products Public Law 90-603 - An Act to amend title 37, United States Code, to clarify the conditions under which physicians and dentists who extend their service on active duty in a uniformed service may be paid continuation pay. Public Law 90-604 - An Act to authorize the disposal of magnesium from the national stockpile Public Law 90-605 - An Act to amend the acts of August 9, 1955, and July 24, 1956, relating to certain common carrier operations in the District of Columbia, and for other purposes Public Law 90-606 - An Act to authorize the establishment of the Biscayne National Monument in the State of Florida, and for other purposes Public Law 90-607 - An Act relating to the effective date of the 1966 change in the definition of earned income for purposes of pension plans of self-employed individuals Public Law 90-609 - An Act to amend sections 281 and 344 of the Immigration and Nationality Act to eliminate the statutory prescription of fees, and for other purposes Public Law 90-610 - An Act to amend the act of August 4, 1950 (64 Stat. 411) to provide salary increases for certain members of the police force of the Library of Congress Public Law 90-611 - Joint resolution extending greetings and felicitations to Saint Louis University in the city of Saint Louis, Missouri, in connection with the one hundred and fiftieth anniversary of its founding PDF | More Public Law 90-612 - An Act to amend title 48 of the United States Code to eliminate certain requirements for the furnishing of nursing home care in the case of veterans hospitalized by the Veterans Administration in Alaska or Hawaii Public Law 90-613 - An Act to amend the joint resolution of March 24, 1937, to provide for the termination of the interest of the United States in certain real property in Allen Park, Mich. Public Law 90-614 - An Act to prescribe administrative procedures for the District of Columbia government Public Law 90-615 - An Act to make permanent the existing suspensions of duty on aluminum oxide when imported for use in producing aluminum, on calcined bauxite, and on bauxite ore Public Law 90-616 - An Act to amend title 5, United States Code, to authorize the waiver, in certain cases, of claims of the United States arising out of erroneous payments of pay to employees of the executive agencies, and for other purposes. Public Law 90-617 - An Act to amend section 2 of the act of June 30, 1954, as amended, providing for the continuance of civil government for the Trust Territory of the Pacific Islands. Public Law 90-618 - An Act to amend title 18, United States Code, to provide for better control of the interstate traffic in firearms Public Law 90-619 - An Act to amend the Internal Revenue Code of 1954 so as to make certain changes to facilitate the production of wine, and for other purposes Public Law 90-620 - An Act to enact title 44, United States Code, ""Public Printing and Documents,"" codifying the general and permanent laws relating to public printing and documents Public Law 90-621 - An Act relating to the income tax treatment of certain statutory mergers of corporations Public Law 90-622 - An Act to amend the Internal Revenue Code of 1954 with respect to the treatment of income from the operation of a communications satellite system Public Law 90-623 - An Act to amend titles 5, 10, and 37, United States Code, to codify recent law, and to improve the code Public Law 90-624 - An Act to amend the Internal Revenue Code of 1954 with respect to the definition of compensation for purposes of tax under the Railroad Retirement Tax Act and for other purposes Public Law 90-625 - An Act to authorize the Secretary of Agriculture to sell to the Village of Central, State of New Mexico, certain lands administered by him formerly part of the Fort Bayard Military Reservation, New Mexico PDF | More Public Law 90-626 - An Act to amend the Federal Property and Administrative Services Act of 1949, as amended, to authorize the rendering of direct assistance to and performance of special services for the Inaugural Committee. Public Law 90-627 - An Act for the relief of Public Utility District No. 1 of Klickitat County, Wash Public Law 90-628 - An Act to repeal certain acts relating to containers for fruits and vegetables, and for other purposes Public Law 90-629 - An Act to consolidate and revise foreign assistance legislation relating to reimbursable military exports Public Law 90-630 - An Act to amend certain provisions of the Internal Revenue Code of 1954 relating to distilled spirits, and for other purposes Public Law 90-631 - An Act to amend title 38 of the United States Code with respect to compensation and educational assistance for widows of veterans to make certain widows and children eligible for care in Veterans Administration hospitals, and to change the limitation of the periods of educational assistance available under part III of such title Public Law 90-632 - An Act to increase the participation of law officers and counsel on courts-martial, and for other purposes Public Law 90-633 - An Act to amend the Immigration and Nationality Act to provide for the naturalization of persons who have served in combat areas in active-duty service in the Armed Forces of the United States, and for other purposes Public Law 90-634 - An Act to extend and amend the Renegotiation Act of 1961 Public Law 90-635 - An Act for implementing Conventions for Free Admission of Professional Equipment and Containers, and for ATA, ECS, and TIR Carnets Public Law 90-636 - An Act to extend certain expiring provisions under the Manpower Development and Training Act of 1962, as amended. Public Law 90-637 - An Act to establish a National Memorial to Woodrow Wilson Public Law 90-638 - An Act to amend the Tariff Schedules of the United States with respect to the rate of duty on certain nonmalleable iron castings Public Law 90-639 - An Act to amend the Federal Food, Drug, and Cosmetic Act to prescribe penalties for the possession of LSD and other hallucinogenic drugs by unauthorized persons Public Law 90-640 - An Act to amend the District of Columbia Public School Food Services Act to provide for the payment of salaries of food service employees from appropriated funds, to provide for adjustments in those salaries, and for other purposes PDF | More Private Law 90-205 - An Act for the Relief of Roberto Perdomo. Private Law 90-206 - An Act for the Relief of Richard K. Jones. Private Law 90-207 - An Act for the Relief of Kelley Michelle Auerbach. Private Law 90-208 - An Act to Authorize the Secretary of the Interior to Exchange Certain Federal Lands for Certain Lands Owned by Mr. Robert S. Latham, Albany, Oregon. Private Law 90-209 - An Act for the Relief of Mrs. Daisy G. Merritt. Private Law 90-210 - An Act for the Relief of John W. Rogers. Private Law 90-211 - An Act for the Relief of Jack L. Good. Private Law 90-212 - An Act for the Relief of James W. Adams and Others. Private Law 90-213 - An Act for the Relief of Manufacturers Hanover Trust Company, of New York, New York. Private Law 90-214 - An Act to Exempt from Taxation Certain Property of the B’nai B’rith Henry Monsky Foundation in the District of Columbia. Private Law 90-215 - An Act to Authorize and Direct the Secretary of the Treasury to Cause the Vessel Ocean Delight, Owned by Saul Zwecker, of Port Clyde, Maine, to be Documented as a Vessel of the United States with Coastwise Privileges. Private Law 90-216 - An Act to Authorize the Use of the Vessel Annie B. in the Coastwise Trade. Private Law 90-217 - An Act for the Relief of Nora Austin Hendrickson. Private Law 90-218 - An Act for the Relief of Doctor Brandla Don (nee Praschnik). Private Law 90-219 - An Act for the Relief of Doctor Jorge Mestas. Private Law 90-220 - An Act for the Relief of Doctor Pedro Lopez Garcia. Private Law 90-221 - An Act for the Relief of Doctor Gabriel Gomez del Rio. Private Law 90-222 - An Act for the Relief of Doctor Jose Ernesto Garcia y Tojar. Private Law 90-223 - An Act for the Relief of Doctor Anacleto C. Fernandez. Private Law 90-224 - An Act for the Relief of Doctor Mario Jose Remirez DeEstenoz. Private Law 90-225 - An Act for the Relief of Seaman Eugene Sidney Markovitz, United States Navy. Private Law 90-226 - An Act for the Relief of Mariana Mantzios. Private Law 90-227 - An Act for the Relief of Ana Jacalne. Private Law 90-228 - An Act for the Relief of Yang Ok Yoo (Maria Margurita). Private Law 90-229 - An Act for the Relief of Susan Elizabeth (Cho) Long. Private Law 90-230 - An Act for the Relief of Lisa Marie (Kim) Long. Private Law 90-231 - An Act for the Relief of Gordon Shih Gum Lee. Private Law 90-232 - An Act for the Relief of Virgilio A. Arango, Doctor of Medicine. Private Law 90-233 - An Act for the Relief of Doctor Alberto De Jough. Private Law 90-234 - An Act for the Relief of Doctor Robert L. Cespedes. Private Law 90-235 - An Act for the Relief of Doctor Angel Trejo Padrou. Private Law 90-236 - An Act for the Relief of Doctor Jose J. Guijarro. Private Law 90-237 - An Act for the Relief of Doctor Edgar Reinaldo Nunez Baez. Private Law 90-238 - An Act for the Relief of Doctor Alfredo Jesus Gonzalez. Private Law 90-239 - An Act for the Relief of Doctor Margarita Lorigados. Private Law 90-240 - An Act for the Relief of Doctor Francisco Guillermo Gomez-Inguanzo. Private Law 90-241 - An Act for the Relief of Doctor Jesus Adalberto Quevedo-Avila. Private Law 90-242 - An Act for the Relief of Doctor Teobaldo Cuervo-Castillo. Private Law 90-243 - An Act for the Relief of Doctor Heriberto Jose Hernandez-Suarez. Private Law 90-244 - An Act for the Relief of Doctor Jesus Jose Eduardo Garcia. Private Law 90-245 - An Act for the Relief of Doctor Noel O. Gonzalez. Private Law 90-246 - An Act for the Relief of Cita Rita Leola Ines. Private Law 90-247 - An Act for the Relief of Doctor Jose Fuentes Roca. Private Law 90-248 - An Act for the Relief of Pedro Antonio Julio Sanchez. Private Law 90-249 - An Act for the Relief of Certain Employees of the Department of the Navy. Private Law 90-250 - An Act for the Relief of the Estate of Josiah K. Lilly. Private Law 90-251 - An Act for the Relief of Chester E. Davis. Private Law 90-252 - An Act for the Relief of Nicholas S. Cvetan, United States Air Force (Retired). Private Law 90-253 - An Act for the Relief of Dennis W. Radtke. Private Law 90-254 - An Act for the Relief of Kap Rai Kim and Young Nam Kim. Private Law 90-255 - An Act for the Relief of Doctor Santiago Jose Manuel Ramon Bienvenido Roig y Garcia. Private Law 90-256 - An Act for the Relief of Angeliki Giannakou. Private Law 90-257 - An Act for the Relief of Suh Yoon Sup. Private Law 90-258 - An Act for the Relief of Yong Chin Sager. Private Law 90-259 - An Act for the Relief of Sandy Kyriacoula Georgopoulos and Anthony Georgopoulos. Private Law 90-260 - An Act for the Relief of Doctor Jose Del Rio. Private Law 90-261 - An Act for the Relief of Victorino Severo Blanco. Private Law 90-262 - An Act for the Relief of Lennart Gordon Langhorne. Private Law 90-263 - An Act for the Relief of Private First Class John Patrick Collopy, US51615166. Private Law 90-264 - An Act to Authorize the Secretary of Agriculture to Grant an Easement Over Certain Lands to the Saint Louis-San Francisco Railway Company. Private Law 90-265 - An Act for the Relief of Donald E. Crichton. Private Law 90-266 - An Act for the Relief of Claud Ferguson. Private Law 90-267 - An Act for the Relief of Lester W. Hein and Sadie Hein. Private Law 90-268 - An Act for the Relief of Lucien A. Murzyn. Private Law 90-269 - An Act for the Relief of Sophie Stathacopulos. Private Law 90-270 - An Act for the Relief of James E. Denman. Private Law 90-271 - An Act for the Relief of Mrs. Esther D. Borda. Private Law 90-272 - An Act for the Relief of Captain David Campbell. Private Law 90-273 - An Act for the Relief of Dean P. Bartelt. Private Law 90-274 - An Act for the Relief of the Estate of Charles C. Beaury. Private Law 90-275 - An Act for the Relief of Mrs. E. Juanita Collinson. Private Law 90-276 - An Act for the Relief of Willard Herndon Rusk. Private Law 90-277 - An Act for the Relief of Captain Russell T. Randall. Private Law 90-278 - An Act for the Relief of Lloyd W. Corbisier. Private Law 90-279 - An Act for the Relief of Earl S. Haldeman, Junior. Private Law 90-280 - An Act for the Relief of John Allunario. Private Law 90-281 - An Act for the Relief of Clara B. Hyssong. Private Law 90-282 - An Act for the Relief of Mary F. Thomas. Private Law 90-283 - An Act for the Relief of Arthur Anderson. Private Law 90-284 - An Act for the Relief of Timothy Joseph Shea and Elsie Annet Shea. Private Law 90-285 - An Act for the Relief of Virgile Posfay. Private Law 90-286 - An Act for the Relief of Certain Individuals Employed by the Department of the Navy at Certain United States Naval Stations in Florida. Private Law 90-287 - An Act for the Relief of Richard Belk. Private Law 90-288 - An Act for the Relief of John M. Stevens. Private Law 90-289 - An Act for the Relief of Robert E. Nesbitt. Private Law 90-290 - An Act for the Relief of Richard C. Mockler. Private Law 90-291 - An Act to Provide for the Conveyance by the Secretary of the Interior of Certain Lands and Interests in Lands in Grand and Clear Creek Counties, Colorado, in Exchange for Certain Lands Within the National Forests of Colorado, and for Other Purposes. Private Law 90-292 - An Act to Authorize the Secretary of the Interior to Consider a Petition for Reinstatement of an Oil and Gas Lease (Wyoming 0310090). Private Law 90-294 - An Act to Authorize the Secretary of the Interior to Reinstate Oil and Gas Lease Las Cruces 063610. Private Law 90-295 - An Act for the Relief of Demetra Lani Angelopoulos. Private Law 90-296 - An Act for the Relief of Miss Amalia Seresly. Private Law 90-297 - An Act for the Relief of Giovanna Ingui Dallara. Private Law 90-298 - An Act for the Relief of Amir U. Khan. Private Law 90-299 - An Act to Confer United States Citizenship Posthumously Upon Private First Class John R. Aneli. Private Law 90-300 - An Act for the Relief of Stanislaw and Julianna Szymonik. Private Law 90-301 - An Act for the Relief of Arley L. Beem, Aviation Electrician's Mate Chief, United States Navy. Private Law 90-302 - An Act for the Relief of Theofane Spirou Koukos. Private Law 90-303 - An Act for the Relief of Donald D. Lambert. Private Law 90-304 - An Act for the Relief of James M. Yates. Private Law 90-305 - An Act for the Relief of Henry Gibson. Private Law 90-306 - An Act for the Relief of Major Hollis O. Hall. Private Law 90-307 - An Act for the Relief of Mrs. Elise C. Gill. Private Law 90-308 - An Act for the Relief of Lieutenant Commander William W. Gentry. Private Law 90-309 - An Act to Authorize the Secretary of the Interior to Convey the Argos National Fish Hatchery in Indiana to the Izaak Walton League. Private Law 90-310 - An Act to Authorize the Secretary of the Army to Quitclaim Certain Real Property in Muscogee County, Georgia. Private Law 90-311 - An Act for the Relief of Peter Balinas and Lee Balinas. Private Law 90-312 - An Act for the Relief of Dwayne C. Cox and William D. Martin. Private Law 90-313 - An Act for the Relief of Mary Jane Orloski. Private Law 90-314 - An Act for the Relief of Louis J. Falardeau, Irva G. Franger, Betty Klemcke, Wineta L. Welburn, and Emma L. McNeil, All Individuals Employed by the Department of the Army at Fort Sam Houston, Texas. Private Law 90-315 - An Act for the Relief of E. L. Townley, Otis T. Hawkins, and Leo T. Matous. Private Law 90-316 - An Act for the Relief of Martina Zubiri Garcia. Private Law 90-317 - An Act for the Relief of Joseph M. Hepworth. Private Law 90-318 - An Act for the Relief of Adel Lessert Bellmard, Clement Lessert, Josephine Gonvil Pappan, Julie Gonvil Pappan, Pelagie Gonvil Franceour de Aubri, Victore Gonvil Pappan, Marie Gonvil, Lafleche Gonvil, Louis Laventure, Elizabeth Carbonau Vertifelle, Pierre Carbonau, Louis Joncas, Basil Joncas, James Joncas, Elizabeth Datcherute, Joseph Butler, William Rodger, Joseph Cote, Four Children of Cicili Compare and Joseph James, or the Heirs of Any Who May Be Deceased Private Law 90-319 - An Act for the Relief of Lydia M. Parsley. Private Law 90-320 - An Act for the Relief of Mrs. Claudette C. Donahue. Private Law 90-321 - An Act for the Relief of Doctor George S. Ioannides. Private Law 90-322 - An Act for the Relief of Doctor Raul Agustin Pereira-Valdes. Private Law 90-323 - An Act for the Relief of Gilmour C. MacDonald, Colonel, United States Air Force (Retired). Private Law 90-324 - An Act for the Relief of Mrs. Sophie Michalowska. Private Law 90-325 - An Act for the Relief of Certain Property Owners in Tate County, Mississippi. Private Law 90-326 - An Act to Authorize and Direct the Secretary of the Interior to Accept Allotment Relinquishments, Approve a Lieu Allotment Selection, and Issue Appropriate Patents Therefor to the Heirs of Dolly McCovey. Private Law 90-327 - An Act to Authorize the Secretary of the Interior to Consider Petition for Reinstatement of Oil and Gas Leases (BLM-A-068348 and BLM-A-068348 (C). Private Law 90-328 - An Act for the Relief of Doctor Earl C. Chamberlayne. Private Law 90-329 - An Act for the Relief of Doctor Violeta V. Ortega Brown. Private Law 90-330 - An Act for the Relief of Doctor Samad Momtazee. Private Law 90-331 - An Act for the Relief of Doctor Bong Oh Kim. Private Law 90-332 - An Act for the Relief of Doctor Hugo Vicente Cartaya. Private Law 90-333 - An Act for the Relief of Doctor Herman J. Lohmann. Private Law 90-334 - An Act for the Relief of Doctor Fang Luke Chiu. Private Law 90-335 - An Act for the Relief of Doctor Julio Epifanio Morera. Private Law 90-336 - An Act for the Relief of Richard Smith (Noboru Kawano). Private Law 90-337 - An Act for the Relief of John Theodore Nelson. Private Law 90-338 - An Act for the Relief of the Ida Group of Mining Claims in Josephine County, Oregon. Private Law 90-339 - An Act for the Relief of Yung Ran Kim. Private Law 90-340 - An Act for the Relief of Heng Liong Thung. Private Law 90-341 - An Act for the Relief of Private Willy R. Michalik, RA 15924409. Private Law 90-342 - Joint Resolution to Grant the Status of Permanent Residence to Maria Mercedes Riewerts. Private Law 90-343 - An Act Conferring United States Citizenship Posthumously upon Staff Sergeant Ivan Claus King. Private Law 90-344 - An Act for the Relief of the Estate of Patrick E. Eagan. Private Law 90-345 - An Act for the Relief of Doctor Chung Chick Nahm. Private Law 90-346 - An Act for the Relief of Anastasia D. Mpatziani. Private Law 90-347 - An Act for the Relief of James T. O'Brien. Private Law 90-348 - An Act for the Relief of Slator C. Blackiston, Junior. Private Law 90-349 - An Act for the Relief of E. Christian Des Marets, Senior. Private Law 90-350 - An Act for the Relief of William W. Hiebert. Private Law 90-351 - An Act for the Relief of Lieutenant (Junior Grade) Herbert F. Swanson, and Others. Private Law 90-352 - An Act for the Relief of Paul L. Margaret, and Jospehine Kirsteatter. Private Law 90-353 - An Act for the Relief of Jose Estrada. Private Law 90-354 - An Act for the Relief of Certain Employees of the Naval Weapons Center, Concord, California. Private Law 90-355 - An Act for the Relief of Henry E. Bullock. Private Law 90-356 - An Act for the Relief of Doctor Ray F. McMillan. Private Law 90-357 - An Act for the Relief of Clifton R. Kindt. Private Law 90-358 - An Act for the Relief of Demetrios Konstantinos Georgaras (also known as James K. Georgaras). Private Law 90-359 - An Act for the Relief of Charles B. Franklin. Private Law 90-360 - An Act for the Relief of Mauritz A. Sterner. Private Law 90-361 - An Act for the Relief of Puget Sound Plywood, Incorporated, of Tacoma, Washington. Private Law 90-362 - An Act for the Relief of Sondra D. Shaw. H. Con. Res. 39 - Bust of Constantino Brumidi--Temporary Placement H. Con. Res. 40 - Best of Constantino Brumidi--Printing of Presentation Proceedings H. Con. Res. 41 - Adjournment--House of Representatives and Senate H. Con. Res. 42 - Warsaw Ghetto Uprising--Anniversary Commemoration H. Con. Res. 43 - The Constitution of the United States H. Con. Res. 44 - Hearings on Establishment of a Commission on Balanced Economic Development and of a Northwest Regional Services Corporation H. Con. Res. 48 - Veterans' Benefits Calculator H. Con. Res. 49 - Anti-Crime Program Hearings H. Con. Res. 50 - ""Summary of Veterans Legislation Reported, Ninetieth Congress"" H. Con. Res. 52 - World Farm Center--Concept H. Con. Res. 54 - United States Capitol Police--Overtime Pay H. Con. Res. 56 - Correction in Enrollment of H. R. 9098 H. Con. Res. 59 - Veterans--Priority in Employment H. Con. Res. 60 - Selected Letters of Vice Admiral Hyman G. Rickover H. Con. Res. 61 - ""The Present-Day Ku Klux Klan Movement"" H. Con. Res. 63 - Signing of Enrolled Bills, Etc. H. Con. Res. 65 - Correction in Enrollment of S. 698 H. Con. Res. 66 - ""Federal Educational Policies, Programs, and Proposals"" H. Con. Res. 67 - ""Commercial Banks and Their Trust Activities: Emerging Influence on the American Economy"" H. Con. Res. 68 - Roth Study--Listing of Operating Federal Assistance Programs S. Con. Res. 45 - ""long-Range Program and Research Needs in Aging and Related Fields"" S. Con. Res. 47 - World Weather Program S. Con. Res. 51 - Committee for Inaugural Arrangements S. Con. Res. 55 - Statues of Father Damian and King Kamehameha I--Acceptance S. Con. Res. 57 - Juvenile Delinquency Hearings S. Con. Res. 58 - ""Status and Future of Small Business"" S. Con. Res. 64 - Corrections in Enrollment of S. 827 S. Con. Res. 69 - Signing of Enrolled Bills, Etc. S. Con. Res. 70 - Adjournment Sine Die Proclamation 3822 - Proclamation to Carry Out Geneva (1967) Protocol to the General Agreement on Tariffs and Trade and Other Agreements Proclamation 3823 - Modifying Proclamation 3279 Adjusting Imports of Petroleum and Petroleum Products Proclamation 3827 - LULAC Week Proclamation 3829 - American History Month, 1968 Proclamation 3833 - Senior Citizens Month, 1968 Proclamation 3838 - National School Safety Patrol Week, 1968 Proclamation 3839 - Death of Martin Luther King, Jr. Proclamation 3840 - Law and Order in the Washington Metropolitan Area Proclamation 3841 - Law and Order in the State of Illinois Proclamation 3842 - Law and Order in the State of Maryland Proclamation 3843 - National Jewish Hospital Save Your Breath Month Proclamation 3846 - White Cane Safety Day, 1968 Proclamation 3849 - Charlotte, North Carolina, Day Proclamation 3851 - Centennial of the Signing of the 1868 Treaty of Peace Between the Navajo Indian Tribe and the United States Proclamation 3853 - Death of Robert F. Kennedy Proclamation 3855 - Amending Proclamation No. 3855, Designating Restricted Waters Under the Great Lakes Pilotage Act of 1960 Proclamation 3856 - Proclamation Amending Part 3 of the Appendix to the Tariff Schedules of the United States with Respect to the Importation of Agricultural Commodities Proclamation 3858 - Family Reunion Day Proclamation 3859 - Salute to Eisenhower Week Proclamation 3861 - Professional Photography Week Proclamation 3863 - American Education Week, 1968 Proclamation 3864 - ""Stay in School"" Proclamation 3865 - National School Lunch Week, 1968 Proclamation 3866 - National Highway Week, 1968 Proclamation 3867 - National Farm-City Week, 1968 Proclamation 3868 - World Law Day, 1968 Proclamation 3869 - National Hispanic Heritage Week, 1968 Proclamation 3872 - Leif Erikson Day, 1968 Proclamation 3874 - National Forest Products Week, 1968 Proclamation 3875 - National Family Health Week Proclamation 3879 - Recognizing the Significant Part Which Harry S. Truman Played in the Creation of the United Nations Reorganation Plan No. 1 of 1968 - Narcotics, drug abuse control Reorganation Plan No. 2 of 1968 - Urban mass transportation Reorganation Plan No. 3 of 1968 - District of Columbia recreation functions Reorganation Plan No. 4 of 1968 - District of Columbia Redevelopment Land Agency Guide to Legislative History of Bills Enacted into Public Law

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Audi's e-tron Plug-In And Electric Cars: Ultimate...

2014-15/0000/en_head.json.gz/1287

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John J. Kruthaupt, 74 Greensburg — John J. Kruthaupt, 74, of Morris, died Monday, March 18, 2013. Visitation is from 10 to 11 a.m. Friday, March 22 at St. Anthony’s Church in Morris. Funeral services follow at 11 a.m., with Rev. Pascal Nduka officiating. Burial in the church cemetery. Memorial to St. Anthony’s Church. Arrangements entrusted to Weigel Funeral Home. Velma Carrie Lutes, 86 April 6, 1928 – April 14, 2014 Velma Carrie Lutes, 86, died Monday, April 14, 2014. Services will be all in one day on Thursday, April 17, at Neal's Funeral Home in Osgood. Visitation is from 10 a.m. to noon and the funeral service will begin at noon, followed by burial in St. Joh Charles R. Bunting, 70 Feb. 1, 1944 - April 10, 2014 Charles R. Bunting, 70, of Greensburg, passed away Thursday, April 10, 2014. Visitation is from noon to 1 p.m. Wednesday, April 16, at Porter-Oliger-Pearson Funeral Home. Funeral services begin at 1 p.m. Wednesday at the funeral home. Online condolen Trysin Aander Ernstes Trysin Aander Ernstes of Greensburg was stillborn Sunday, April 13, 2014 at St. Vincent Women's Hospital in Indianapolis. He was the son of Tiffani J. Venable and Charles Ernstes II, of Greensburg. Other survivors include his sisters, Jastin Venabl Margaret E. Giesting-Jones, 80 Sept. 1, 1933 – April 11, 2014 Margaret E. Giesting-Jones, 80, of Batesville, passed away on Friday, April 11, 2014. She was born Sept. 1, 1933, the daughter of Robert E. and Ethel (Jackson) Martin. She married John Giesting on Oct. 25, 1958, and he preceded her in death on Dec. L. Jerry Lee 81 Nov. 1, 1932 - April 12, 2014 (PLEASE USE THE FLAG - VETERAN) L. Jerry Lee, 81, of Greensburg, passed peacefully away Saturday, April 12, at Arbor Grove Village, Greensburg. He was born Nov. 1, 1932, a son of the late Louise (Schwagmeier) and Lloyd E. Lee. He was the husband of A Susan M. Huffmeyer, 48 Sept. 24, 1965 – April 10, 2014 Susan M. Huffmeyer, 48, of Napoleon, passed away Thursday, April 10, 2014, at her home. She was born in Batesville on Sept. 24, 1965, the daughter of Raymond and Rose (Simmermeyer) Weisenbach. She was a 1983 graduate of East Central High School and Loretta T. Blankman, 84 Loretta T. Blankman, 84, of Greensburg, passed away Friday, April 11, 2014 at Columbus Regional Hospital in Columbus. Born April 28, 1929 in Harrison, Ohio, she was the daughter of Elmer and Elizabeth (Hoerst) Roell. Loretta was a member of St. Mary' Bruce Flannery, 56 June 6, 1957 - April 10, 2014 Bruce Flannery, 56, of North Vernon, passed away Thursday, April 10, 2014. Funeral services begin at 11 a.m. Monday, April 14, at Dove-Sharp & Rudicel Funeral Home, North Vernon. Friends may call from 4 to 8 p.m. Sunday, April 13, at the funeral home Hugh Smith November 13, 1946 - April 9, 2014 Hugh Smith, 67, Greensburg, passed away at his Greensburg residence. Hugh was born in Manchester, Ky., November 13, 1946, a son of the late Alice (Maxie) and Theo Smith. Grave Side Funeral Service will be in Westport Cemetery, at 11 a.m., April 12.

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Ed's Blog Edgar Rice Burroughs' "A Princess of Mars": The First Appearance of John Carter By Ed on March 8, 2012 9:16 AM Back in August 2010, I reviewed Edgar Rice Burroughs' first novel A Princess of Mars, which is the source material for the upcoming John Carter movie opening this Friday. Here's what I had to say about the book. In 1911, Edgar Rice Burroughs (1875-1950), a failed businessman who had been working in a series of various dead-end clerical jobs and was desperate to feed his family, submitted a story to the then-popular pulp magazine All-Story under the pen name of "Normal Bean" (changed by somebody in editorial to "Norman Bean"). The story, originally titled Under The Moons of Mars, was picked up and serialized by All-Story in 1912 and became a popular hit with readers, resulting in a successful literary career for Burroughs (whose third novel was Tarzan of the Apes in 1914, having also been serialized in All-Story two years before). Under the more familiar title A Princess of Mars, Burroughs' first story also inaugurated the popular "Martian" series of adventures when first published in book form in 1917. Even without all that background, A Princess of Mars is still an exciting (if scientifically inaccurate and somewhat politically incorrect) action-adventure/fantasy tale. Beginning in 1866, Civil War veteran and prospector John Carter, while escaping from Indians, is inexplicably transported, apparently serveral hundred centures in the past, to the planet Mars. Falling in with the green-skinned, four armed warriors the Tharks, Carter (who discovers that the natives' name for their planet is "Barsoom"), finds he's developed amazing strength and abillities due to the planet's atmosphere and quickly proves his worth as a fighter and eventually, with help by Tharkian Tars Tarkas, rises in the group's hierarchy. However, the Tharks' capture of a beautiful red-skinned, human princess named Dejah Thoris gets Carter all inflamed by passion. Carter frees Dejah while making their escape from her captors and then becomes imbroiled in palace intrigue between the Red Martians of Helium and the Tharks as well as battling the forces of neighboring Zodanga. Eventually Carter settles down with Dejah and becomes Prince of Helium. But then, just as things look good... A good old-fashioned swashbuckler (Carter and the various Barsoomians use swords because...well, read for yourselves) romance, A Princess of Mars (click here to reserve a copy) was and still is an influencial work of the science fiction/fantasy genre. It also has a terrific "sweep" style of storytelling, with Burroughs constantly moving Carter and the other characters from one situation to the next with barely a chance to breathe. Burroughs also masterfully succeeds in creating fantasically detailed backstories and customs for the Barsoomians. And the nail-biting cliffhanger ending is Burroughs at his best. Aside from the first two sequels The Gods of Mars and The Warlord of Mars, Burroughs's other Martian novels are currently out-of-print. Here's hoping the upcoming Disney film adaptation (due in 2012) changes that situation! Looks like the situation did change. Click here to see what I mean.and look at the other movie-related titles we carry here. In the next few weeks I'll be reviewing the other installments in the original series. Tags: A Princess of Mars, Edagr Rice Burroughs, John Carter Bean Green | March 9, 2012 11:16 AM Been a fan of this series since 1975. When I first picked up the book "A Princess of Mars". I will be there today the 9th of March to see this film. Hopefully it will remain true to the Burroughs book. Ed replied to comment from Bean Green Hope you enjoyed it Bean! John Cronin I FIRST RED PRINCESS OF MARS AROUND 30 YEARS AGO. I WAS FASCINATED WITH THE STORY BECAUSE IT STIRRED YOUR IMAGINATION. BACK THEN THE IDEA OF THIS STORY BEING MADE INTO A MOVIE WAS CRAZY ALTHOUGH I THOUGHT SOMEDAY WITH THE TECHNOLOGY WE DEVELOP THAT IT WOULD BE POSSIBLE TO MAKE A MOVIE OUT OF HIS BOOKS. LO AND BEHOLD IT IS HAPPENING. I CAN'T WAIT TO SEE THE MOVIE AND RECOLLECT THE STORY. HOPE IT CONTINUES SUCCESSFULLY We want to hear from you. Feel free to post comments, questions and other thoughts but please remember: Stay on topic. Be polite and respectful Don’t post copyrighted materials Please don’t post content that installs viruses, worms, etc. No spam please. Please see our Comment Guidelines page for more information. Greenwich Library ADA page Got a question and can't get to the library? Contact Ask-A-Librarian. Beat Literature (6) Career and Employment (100) Classic & Cult Television (27) For Persons with Disabilities (211) Library Stuff (4) Science Fiction, Fantasy & Horror (150) Cult Films (2) About Ed's Blog Tweets by @EPMJRR About this Entry This page contains a single entry by Ed published on March 8, 2012 9:16 AM. Proyecto Vision was the previous entry in this blog. Happy 90th Birthday Jack Kerouac! is the next entry in this blog.

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Home > Health Encyclopedia > Health Encyclopedia Home Pediatric Information Health Encyclopedia Home Obesity in AdolescentsObesidad What is obesity? Overweight and obesity together represent the second leading preventable cause of death in the United States. Obesity is a serious, chronic disease that can inflict substantial harm to a person's health. Overweight and obesity are not the same; rather, they are different points on a continuum of weight ranging from being underweight to being morbidly obese. The percentage of people who fit into these two categories, overweight and obese, is determined by body mass index (BMI). Public health professionals agree that overweight and obesity have reached epidemic proportions in this country. Public health officials say physical inactivity and poor diet are catching up to tobacco as a significant threat to health. According to the most recent data from the 2003-2006 National Health and Nutrition Examination Survey, one out of five or 17 percent of U.S. children, ages 6 to 19, are overweight or obese. In addition, more than two-thirds of the U.S. population is overweight or obese--over 64 percent of women and 72 percent of men. However, for the first time in decades, the prevalence of U.S. adult obesity is not rising. BMI is a measure of weight proportionate to height. BMI is considered a useful measurement of the amount of body fat. Occasionally, some very muscular people may have a BMI in the overweight range. However, these people are not considered overweight because muscle tissue weighs more than fat tissue. Generally, BMI can be considered an effective way to evaluate whether a person is overweight or obese. What causes obesity? In many ways, obesity is a puzzling disease. How the body regulates weight and body fat is not well understood. On one hand, the cause appears to be simple in that if a person consumes more calories than he or she expends as energy, then he or she will gain weight. However, the risk factors that determine obesity can be a complex combination of genetics, socioeconomic factors, metabolic factors, and lifestyle choices, as well as other factors. Some endocrine disorders, diseases, and medications may also exert a powerful influence on an individual's weight. Factors which may influence the occurrence of obesity include, but are not limited to, the following: Genetics--Studies have shown that a predisposition toward obesity can be inherited. Although researchers have identified several genes that appear to be associated with obesity, most believe that one gene is not responsible for the entire obesity epidemic. The majority of current and future research aims to better understand the interaction between these gene variations and our ever-changing environment in the development of obesity. Metabolic factors--How a particular person expends energy is different from how someone else's body uses energy. Both metabolic and hormonal factors are not the same for everyone, but these factors play a role in determining weight gain. Recent studies show that levels of ghrelin, a peptide hormone known to regulate appetite, and other peptides in the stomach, play a role in triggering hunger and producing a feeling of fullness (satiety). Socioeconomic factors--There is a strong relationship between economic status and obesity, especially among women. Women who are poor and of lower social status are more likely to be obese than women of higher socioeconomic status. The occurrence of obesity is also highest among minority groups, especially among women. Lifestyle choices--Overeating, along with a sedentary lifestyle, contributes to obesity. These are lifestyle choices that can be affected by behavior change. Eating a diet in which a high percentage of calories come from sugary, high-fat, refined foods promotes weight gain. And, as more U.S. families eat on the go, high-calorie foods and beverages are often selected. Lack of regular exercise contributes to obesity in adults and makes it difficult to maintain weight loss. In children, inactivity, such as watching television or sitting at a computer, contributes to obesity. Who is affected by obesity? Physical factors contributing to excess body fat in adolescents include the following: Increased insulin levels Elevated lipid and lipoprotein levels Behavioral and other factors contributing to a positive energy balance stored as fat over long periods of time include the following: Excessive intake of high energy foods Inadequate exercise in relation to age More sedentary lifestyle Low metabolic rate Increased insulin sensitivity What are the symptoms of obesity? The following are the most common symptoms that indicate an adolescent is obese. However, each adolescent may experience symptoms differently. Symptoms may include: Facial features often appear disproportionate Adiposity (fat cells) in the breast region in boys Large abdomen (white or purple marks are sometimes present) In males, external genitals may appear disproportionately small Puberty may occur early Increased adiposity in the upper arms and thighs Genu valgum (knock kneed) is common Adolescents who are obese often experience significant social pressure, stress, and difficulties accomplishing developmental tasks. Psychologic disturbances are also very common. The symptoms of obesity may resemble other conditions or medical problems. Always consult your adolescent's doctor for a diagnosis. Health effects of obesity Obesity has a far-ranging negative effect on health. Each year obesity-related conditions cost over 100 billion dollars and cause premature deaths in the U.S. The health effects associated with obesity include, but are not limited to, the following: High blood pressure--Additional fat tissue in the body needs oxygen and nutrients in order to live, which requires the blood vessels to circulate more blood to the fat tissue. This increases the workload of the heart because it must pump more blood through additional blood vessels. More circulating blood also means more pressure on the artery walls. Higher pressure on the artery walls increases the blood pressure. In addition, extra weight can raise the heart rate and reduce the body's ability to transport blood through the vessels. Diabetes--Obesity is the major cause of type 2 diabetes. Obesity can cause resistance to insulin, the hormone that regulates blood sugar. When obesity causes insulin resistance, the blood sugar becomes elevated. Even moderate obesity dramatically increases the risk of diabetes. Heart disease--Atherosclerosis (hardening of the arteries) occurs more often in obese people compared to those who are not obese. Coronary artery disease is also more prevalent because fatty deposits build up in arteries that supply the heart. Narrowed arteries and reduced blood flow to the heart can cause chest pain (angina) or a heart attack. Blood clots can also form in narrowed arteries and cause a stroke. Joint problems, including osteoarthritis--Obesity can affect the knees and hips because of the stress placed on the joints by extra weight. Joint replacement surgery, while commonly performed on damaged joints, may not be an advisable option for an obese person because the artificial joint has a higher risk of loosening and causing further damage. Sleep apnea and respiratory problems--Sleep apnea, which causes people to stop breathing for brief periods, interrupts sleep throughout the night and causes sleepiness during the day. It also causes heavy snoring. Respiratory problems associated with obesity occur when added weight of the chest wall squeezes the lungs and causes restricted breathing. Sleep apnea is also associated with high blood pressure. Cancer--In women, being overweight contributes to an increased risk for a variety of cancers including breast, colon, gallbladder, and uterus. Men who are overweight have a higher risk of colon and prostate cancers. Metabolic syndrome--The National Cholesterol Education Program has identified metabolic syndrome as a complex risk factor for cardiovascular disease. Metabolic syndrome consists of six major components: abdominal obesity, elevated blood cholesterol, elevated blood pressure, insulin resistance with or without glucose intolerance, elevation of certain blood components that indicate inflammation, and elevation of certain clotting factors in the blood. Psychosocial effects--In a culture where often the ideal of physical attractiveness is to be overly thin, people who are overweight or obese frequently suffer disadvantages. Overweight and obese persons are often blamed for their condition and may be considered to be lazy or weak-willed. It is not uncommon for overweight or obese conditions to result in persons having lower incomes or having fewer or no romantic relationships. Disapproval of overweight persons expressed by some individuals may progress to bias, discrimination, and even torment How is obesity diagnosed? Obesity is diagnosed by a doctor. The body mass index (BMI) is usually used to define obesity in adolescents. Two categories are defined, including the following: BMIs at the 95th percentile or more for age and sex or BMIs of more than 30 (whichever is smaller). BMI findings in this category indicate the need for a complete medical work-up. BMIs between the 85th and 95th percentile or BMIs equal to 30 (whichever is smaller) suggest a second level screening which includes evaluation of five areas of health risks including the following: Family history of cardiovascular disease, parental elevated total cholesterol, diabetes, parental obesity Total cholesterol level Large increases in BMI assessments from year to year Concerns about weight, including personal (emotional or psychological) concerns related to weight and perception of self as overweight Treatment for obesity Specific treatment for obesity will be determined by your adolescent's doctor based on: Your adolescent's tolerance for specific medications, procedures, or therapies Treatment for obesity in adolescents may include the following: Nutritional and individual diet counseling Modification of diet and caloric content Increased exercise or participation in an appropriate exercise program Individual or group therapy focused on changing behaviors and confronting feelings related to weight and normal developmental issues Support and encouragement for making changes and following recommended treatment recommendations Treatment planning to address the above components often includes the involvement of a nutritionist, qualified mental health professionals, and an exercise specialist. Treatment goals should be realistic, focused on modest reduction of intake, changes in eating habits, and the incorporation of a healthy exercise-oriented lifestyle. Prevention of obesity Young people generally become overweight or obese because they do not get enough physical activity in combination with poor eating habits. Genetics and lifestyle also contribute to a child's weight status. Recommendations for prevention of overweight and obesity during childhood and adolescence include: Gradually work to change family eating habits and activity levels rather than focusing on a child's weight. Be a role model. Parents who eat healthy foods and participate in physical activity set an example so that a child is more likely to do the same. Encourage physical activity. Children should have 60 minutes of moderate physical activity most days of the week. More than 60 minutes of activity may promote weight loss and subsequent maintenance. Reduce "screen" time in front of the television and computer to less than two hours daily. Encourage children to eat when hungry and to eat slowly. Avoid using food as a reward or withholding food as a punishment. Keep the refrigerator stocked with fat-free or low-fat milk, fresh fruit, and vegetables instead of soft drinks and snacks high in sugar and fat. Serve at least five servings of fruits and vegetables daily. Encourage children to drink water rather than beverages with added sugar, such as soft drinks, sports drinks, and fruit juice drinks. Teen Health Quiz Your Child's Growth and Development Breast Conditions

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ADDING EX-CELLENCE by Logan Buckley - griffinshockey.com After two seasons out of the AHL playoff picture, the Grand Rapids Griffins are retooled, toughened up and on a mission to emulate their parent club, the Detroit Red Wings, by marching into the post-season. Similar to the structure in Detroit where stability on the backend is the foundation upon which the team is built, the Griffins made a few key moves in an effort to shore up their defense for the 2011-12 season. Chief among them was the addition of veteran defenseman Garnet Exelby. With 408 NHL games between Atlanta Thrashers and Toronto Maple Leafs under his belt, Exelby is a proven commodity known for physically erasing opponents from the game. “We tried to level the playing field in the physical department in the past here, and hopefully it was effective for us. With Garnet here now we’ve leveled the playing field with one guy,” said Griffins head coach Curt Fraser. “It’s the way he plays, the way he competes on the ice – he’s tough. He’s got that edge to him and all the players in the league are aware of that.” Fraser also points out that Exelby does a lot of things very well and is more than just a tough-as-nails defenseman. “He’s strong, blocks shots and does anything to win.” Exelby echoed his coach when describing the overlooked aspects of his game. “I like to be a strong penalty killer and block shots. Any chance I can get to block shots and help the goaltender out I’ll do that. I always want to be a plus player; I hate getting scored on in any facet,” he said. Exelby began his pro career 10 years ago with the Chicago Wolves, playing a season and a half with the AHL club before graduating to Atlanta. It was at that time when he first met Fraser, who was then coach of the Thrashers. While Exelby never played directly under Fraser in Atlanta, the coach knew they had a future NHLer in the system. “We knew all about Garnet. At that time, we were a team just kind of growing slowly, and some of the young guys they didn’t bring in too fast. But I left and then Garnet became a big part of that team and was a very, very good player,” said Fraser. “He played in a situation in Atlanta where the kids had to grow up fast and had to learn how to play the game real quick. It was probably tough to work through, but he did a good job for them. Now he’s moved around a little bit, but we welcome him with open arms here. He’s exactly what we needed,” Fraser added. This will be Exelby’s third straight year with a new team, having played a single season for the Rockford IceHogs last year and Toronto in 2009-10. Yet, the new surroundings have not fazed Exelby. Veteran Griffins defenseman Greg Amadio observed that Exelby has seamlessly transitioned into the Grand Rapids locker room. “I think it’s not that hard for him. He’s been around pro hockey for a long time, been in every situation. He’s got over 400 games in the NHL; he’s familiar with our league. This group’s only been together for a short time, but we’re coming together pretty quick and he’s doing a good job,” said Amadio. While Exelby does bring physicality to the Griffins’ defense, he will also be counted on for his experience and leadership, as he replaces long time Griffin Jamie Tardif as captain. “It’s always an honor. There are many great leaders in this locker room, and I hope we can all mesh together and share the load because I think that’s what a great team will do,” said Exelby of donning the “C” on his sweater in his first year with the club. Exelby’s professional experience is a big draw for the Griffins. While the team has numerous players returning from last season, the average age of the squad is just over 24 years old and Exelby, along with fellow defensemen Amadio and Doug Janik and forward Chris Conner, will be counted on to lead the team both on and off the ice. “Looking back, it wasn’t that long ago that I was one of the younger guys kind of looking to some veteran guys, trying to learn the ropes and figure out how to try and succeed in this game. Now I’m on the other side, I’m sort of the big brother in a way. It’s an exciting role for me,” said Exelby. With a Calder Cup, won as a rookie in 2001-02 with Chicago, already on his shelf, Exelby knows what it takes to go the distance. It’s the one thing he hopes all his teammates get a chance to experience as well. “I can’t think of any more valuable experience that I’ve had over the years than the 25 or so playoff games I played in that year. Just to be under that pressure of the game sevens, bouncing back after a tough loss, the travel, and going through that kind of grind with some teammates and guys who are pretty special to me, and to be successful and to close it out – it’s valuable experience,” said Exelby. “I would hope that every young player in here gets a chance to go deep. I hope they can win a championship, but to go deep in the playoffs at some point in their career and learn what it takes and what it’s going to be like.” Just a step away from the playoffs last year, the Griffins will count on Exelby to help solidify the defensive foundation of a team that expects to be in playoff contention come April.

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Call Center Customer Service Representative665 DELAWARE AVENUEMARION, OH 43302 Pizza Hut is committed to breakthrough innovation and the success of our employees. From our world class operations to our passionate customer mania philosophy and an incredible franchise system, this is one great place to work! So come see what it's like to be with a global leader in the restaurant industry. You'll find a fun, fast paced and supportive culture, where all of our success comes from our belief in people, and investing in you is our top priority. Working at Pizza Hut is about making hungry people happy. It’s about being independent and having fun, making new friends and earning extra cash. As a Pizza Hut Call Center Customer Service Representative you’ll be a friendly person who is comfortable talking on the phone. You’ll need to communicate with our customers so that they know their orders and concerns are your number one priority. You’ll have attitude - the right kind of course - and understand the need to be on time, all the time. With loads of energy, you understand that work is easier – and more fun – with teamwork.

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GTAGaming Forums (http://www.gtagaming.com/forums/index.php) - Multiplayer (http://www.gtagaming.com/forums/forumdisplay.php?f=299) - - Liberty City Life(XBOX 360) (http://www.gtagaming.com/forums/showthread.php?t=134975) lacrosseguy1123 Liberty City Life(XBOX 360) Start of the Game - Players begin the game with $7,000 that can be used to purchase whatever they wish and give them a jump-start to success. Death (Police Disregard This) - If you are killed by another player (non-execution) you must act out the death as an injury depending on where and how you were injured. You must return to the location of your injury after you respawn and act out everything accordingly such as going to the hospital. Housing and Businesses - Players are often interested in buying property to live in or work out of. In order to do this, they must search through the property list. If you wish to start a business such as a cab service, head shop or anything else you need a building to operate out of. Only one house may be purchased per player, but any amount of people may stay in an already purchased home if the owner gives them permission whether for rent or free. The only way to collect revenue from a business is to have someone working at it for a daily shift or a steady A.I. worker that is paid just as a regular worker would. If you are a business owner you may work at a maximum of two of your businesses yourself, but you will need to hire additional workers if you wish to collect revenue for 3 or more businesses. The bank can not be scammed IC by an OOC loophole. You can try and not pay your loan IC and risk being arrested but any blatant scamming of the system such as willing the money or giving it to a friend...etc will result in OOC action. Play Your Role - You must abide by the rules of your chosen characters lifestyle. This means that if you are a civilian, you will not be participating in assassinations, firefights with the cops, or robbing other players. If you do murder someone, it must be with roleplay purposes (they were holding you hostage and an opportunity for escape presented itself, you went crazy when you saw them because they tried to kill you previously). Do as a real life equivalent of your character would do in everyday life. Purchasing a Weapon - Weapons may be purchased legally from the gun dealer or they can be purchased illegally from the black market (gangs). A gun purchased from the dealer will give the customer a license which allows them to keep the gun if they are arrested for a non-gun related crime. If they have a gun without a license it will be taken no matter what from police during any arrest and the player will receive a fine and jail time. The gun dealer may only sell non-automatic weapons including the knife, pistol(s), shotgun(s), and sniper. Any automatic weapon is considered illegal if used by a non-police officer and can only be purchased via the black market. You may not sell "single-fire" automatic weapons because that will get abused. Knockout - If two players are in a fistfight and one of the players beats the other to a very low health they "knock them out". The player with the lower health must have his character be unconscious. He does not hear anything that the other players are saying and must do anything that they say. Facial Reconstruction - If you wish to change the physical appearance of your character for whatever reason you have the option of facial reconstruction. It will be an advanced procedure that will take up to a day to complete. The recovery period will take the rest of the roleplay. A person can only change to a face of the SAME race. It will cost $3000, which you can take a loan for. Vehicles - Players will automatically be provided with a Standard Drivers License that allows them to drive cars, buses, trucks...etc, however they must purchase additional licenses if they wish to operate vehicles such as Motorcycles, Boats, and Helicopters. Players may drive illegally, but if they are caught by police they will pay a heavy fine and do an extended jail sentence. State Owned - If a property is owned by the state, it is temporarily owned by the host just as a means for players to get jobs. State owned properties CAN BE PURCHASED. Gangs - Gangs may be established in-game if players meet together and wish to form a criminal empire. The roleplay will be limited to three gangs with a maximum of 4 players per gang, and if you wish to create a gang you must fill out an application in the gang page. Only 2 gangs will be allowed in each role play unless stated otherwise by the hoster, with a maximum of 3 players per gang on a first come first served basis. Gangs are required to make a post on the website with information about themselves including a ranking system, member list, owned property list, and history if they get their application accepted. Do not create a gang post if your gang hasn't been validated. Drugs - Drugs are to be sold by a dealer in-game whether it be a lone criminal, or a gang outfit. Drugs may be imported from ship, grown, or purchased from a doctor and/or other dealers. Suggested prices are posted below, but you do not have to follow them. As a drug dealer you may purchase the required items to grow and/or make a drug from the general store. You must designate the location of your grow op to a staff member before you start to grow/make your product. The prices for items will be listed on the general store post. The only items that dealers can grow are meth and weed. Any other drug must be imported or purchased from a doctor. If you are a criminal you have the option to import drugs through vehicular transport. This option has the most customization. You will make a legitimate system for importing your drugs and ask a staff member about it. If they OK it then you are set to go. One of the main options is to manually boat the drugs to the city. This will be done by driving your boat to the corner of the map on the ocean and stay th

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About GNS Business/Industry Maritime Medical News Opinion/Forum State of Louisiana State of Mississippi Elementary and Primary Education Jim Guidry Commentaries Mardi Gras Holiday Happenings Juneteenth Fourth of July Higher Education Texas A&M University System Overall 2 percent decrease from FY 2011 projected COLLEGE STATION – The Texas A&M University System Board of Regents today approved a $3.3 billion budget that will fund operations at its 11 universities, seven state agencies, health science center, and central administrative offices in FY 2012. The FY 2012 budget is reflective of a 2 percent, or $70.7 million, decrease in operational activities funded by all revenue sources when compared to FY 2011. The budget reflects increased revenues to capture systemwide enrollment growth projected at 4 percent, as well as an additional $121 million appropriated to the Texas Forest Service to cover the costs incurred in fighting the state’s wildfires. Also, in an effort to keep the cost of attending A&M System universities affordable, there were no increases to the overall designated tuition rates, with the exception of specific targeted differential designated tuition increases. The new budget will take effect Sept. 1. The FY 2012 operating budgets for the A&M System universities and agencies are: Prairie View A&M University $170.9 million Tarleton State University $126.9 million Texas A&M International University $84.4 million Texas A&M University $1.2 billion Texas A&M University at Galveston $45.5 million Texas A&M University-Central Texas $26.2 million Texas A&M University-Commerce $131.3 million Texas A&M University-Corpus Christi $146.5 million Texas A&M University-Kingsville $109.1 million Texas A&M University-San Antonio $34.7 million Texas A&M University-Texarkana $23.2 million West Texas A&M University $115.9 million The Texas A&M Health Science Center $194.4 million Texas AgriLife Research $184.9 million Texas AgriLife Extension Service $111.3 million Texas Forest Service $49.2 million Texas Veterinary Medical Diagnostic Laboratory $16.6 million Texas Engineering Experiment Station $148.5 million Texas Engineering Extension Service $82.5 million Texas Transportation Institute $61.5 million System Offices Operations $30.5 million Debt Service $251.5 million TOTAL $3.3 billion The operating budget includes, among other funding sources, tuition and fee revenue increases of $37.7 million, or 4 percent. Expenditures include $1.9 billion to cover personnel costs, which accounts for 56 percent of the total operating budget. An executive summary of the FY 2012 budget is available online at: http://www.tamus.edu/offices/budget-acct/budget/summary/ About the A&M System The A&M System is one of the largest systems of higher education in the nation, with a budget of $3.3 billion. Through a statewide network of 11 universities, seven state agencies and a comprehensive health science center, the A&M System educates more than 120,000 students and makes more than 22 million additional educational contacts through service and outreach programs each year. Externally funded research expenditures exceed $772 million and help drive the state’s economy. Guidry News Service is headquartered in Midtown Houston. at 4001 Fannin Street, Suite 4432, Houston, TX. 77004-4077 (409) 763 NEWS(6397) News@GuidryNews.com © 1996, Guidry News Service. Duplication of any part of this website in any manner is prohibited.

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Home » Research Methods » Qualitative Research Print Create Flyer Bestseller Five Ways of Doing Qualitative Analysis Phenomenological Psychology, Grounded Theory, Discourse Analysis, Narrative Research, and Intuitive Inquiry Frederick J. Wertz, Kathy Charmaz, Linda M. McMullen, Ruthellen Josselson, Rosemarie Anderson, and Emalinda McSpadden Size: 6⅛" x 9¼"Paperback order Professors: free copies available for adoption consideration Download an e-book copy now or request a print copy “The authors strike a balance between providing a valuable beginner's resource and staying true to the critical spirit of a complex tradition....The opening history goes from strength to strength, making a case for the legitimacy of and precedent for qualitative methods. Continuing into a story of the development of different threads of qualitative work, the authors do an excellent job showing the emergence of different methodologies in response to particular questions and circumstances....The authors offer an abundance of resources in the forms of important citations, centers for qualitative research, and online resource banks....Provides good resources and concise examples of how different theoretical perspectives would shape a project, as well as showing in its structure and style the type of discourse that makes qualitative inquiry unique....An exemplary introduction to the field and should serve as a valued reference for years to come.”—PsycCRITIQUES “What was most illuminating was how each researcher offers reflective comments on one another's analysis of the data. These collegial meta-commentaries are perhaps the most unique and noteworthy feature of the entire project. These transparent assessments of one another's analysis offer the reader not just a comparison of five diverse modes of qualitative research but penetrating insights into the essence of qualitative research and the very meaning of qualitative psychology. There is no other text like this....Throughout the text we see Wertz, like a good committee chair, weaving between all five approaches, and sewing together a consensus....For advanced graduate students or seasoned professionals this material is an indispensable resource, especially for those who are seeking a qualitative method most appropriate to their research goals. There is no better book for understanding and promoting qualitative research as a general field of psychological inquiry....Serves as a virtual Rosetta stone that can bring together an unwieldly field perpetually under risk of fragmentation into a generative and disciplined research community....The style of mutual respect and careful engagement we witness in this collaborative project is itself exemplary of the attitude of scientific openness and collegiality that, more than anything will eventually transform psychology into the liberatory science it was always meant to be.”—Journal of Phenomenological Psychology “Provides both novice and seasoned researchers with an engaging and active approach to many dimensions of qualitative research. Although one text cannot possibly be expected to address all of the demands of qualitative research….The six authors have achieved so much in this book that a thorough, but concise review is challenging, given that there is so much to recommend….The authors provide an excellent model for collaboration, one that is extremely reflexive, and which should be of interest to all, but may be of particular interest to graduate students and newer scholars who may assume that the processes of researching and writing are unproblematic and uneventful….The inclusion of The Teresa Texts provides readers with the opportunity to fully understand how researchers approach data, but would also provide students with the opportunity to undertake their own analyses and compare them to those shared by the first five authors….This is a dynamic and comprehensive text. It is a ‘must read’ for anyone who is at all interested in qualitative research and it promises to foster much dialogue among both teachers and students of qualitative methods.”—British Journal of Psychology “A range of traditional and creative methods are described and, perhaps most significantly, the authors emphasize researcher subjectivity. They offer compelling reflexive examinations of their horizons and personal presences in the process of research—a bold move in tune with the spirit of the qualitative enterprise….The depth and breadth of the work of these visionaries is astonishing. Qualitative research has surely come of age….This is an extraordinary and challenging book. Its accessible writing style and provision of practical examples will appeal to those new to the field….The full data set and step-by-step guidance offered makes this a valuable resource. For experienced researchers, the book offers nuanced and penetrating glimpses into other methodological worlds not normally visited while its innovative comparative approach usefully challenges taken-for-granted understandings. The book provides both novice and expert privileged access to a series of inspirational, mutually respectful masterclasses on how to conduct meticulous in-depth analysis.”—The Humanistic Psychologist “This is a courageous book, and its success is due precisely to the openness and audacity of its authors….This book is an extraordinarily valuable contribution to qualitative research pedagogy. The style of the book draws the reader into the material and makes the reader want to do some analysis of it oneself….The book could be used to provide master classes in textual analysis for students who already have some acquaintance with a few of the approaches dealt with in the book.”—The Indo-Pacific Journal of Phenomenology “A text that simultaneously provides depth and breadth. Beginning with a discussion of how innovative and creative qualitative approaches led to the five methodologies examined, the authors provide valuable historical context….The first third of the book could stand alone as an introduction to the evolving history of qualitative research.…I can say without reservation that this is a text that I’ll continue to recommend and revisit.”—The Qualitative Report “An extraordinary achievement. This is the book I will recommend to my quantitative colleagues when they ask, 'Just what is qualitative research?' Unlike other books that give steps for doing a qualitative study, Five Ways takes the reader into the thoughts and feelings involved in conducting research. The exciting, informative interactive discussions among the researchers and the participant provide unique insights. I will use Five Ways as the basic text in my qualitative courses.”—Donald E. Polkinghorne, PhD, Professor Emeritus, Department of Counseling Psychology, University of Southern California “Not only do the authors look at a common data set in five different ways, but they also reflect on how all five analyses look to each of them, and these explorations are 'looked back at' by the participant from whom the data set was derived. This book provides an engaging and intimate view of the many selves it takes to bring qualitative analyses into being and the reflexive practices that contribute to the scientific and ethical integrity of research.”—Margarete Sandelowski, PhD, RN, FAAN, School of Nursing, University of North Carolina at Chapel Hill “This unique work is a wholly absorbing adventure in comparative methodology. For the student, it will serve as an effective and informative introduction to a range of central qualitative methodologies. For the seasoned scholar, it provides a wonderfully nuanced view of the complex processes of decision making in qualitative inquiry. The book challenges us to grapple with major issues: the goals of our work, its functions in the social world, and its ethical implications. This is a landmark work in the development of qualitative inquiry.”—Kenneth J. Gergen, PhD, Department of Psychology, Swarthmore College “The logic of the book is transparent: it presents a narrative, multiple interpretations, and a comparison of the varied interpretations. The experience of walking through the various interpretations and then seeing how experts unpack the differences and similarities among them is remarkable. Although many books are written for introductory courses on qualitative methods, very few authors attend to how the structure of a text—not just its content—might be pedagogically significant. I applaud Wertz et al. for thinking explicitly and intentionally about how to conceptualize and organize their text in a way that facilitates learning.”—Suzanne M. Wilson, PhD, Department of Teacher Education and Director, Center for the Scholarship of Teaching, Michigan State University “This text addresses one of the most frequently asked questions in qualitative analysis: what is the difference between phenomenology, grounded theory, discourse analysis, narrative research, and intuitive inquiry? The authors explain the theory that underlies each approach and illustrate its application and the resultant findings, making the book a worthy text for a qualitative methods course. As an added bonus, the authors present the participant's reaction to the results of the five different analyses and discuss the ethical implications in terms of letting the participant speak for herself, issues of confidentiality, and tensions around interpretation of data. I would definitely use this book in my advanced qualitative research course.”—Donna M. Mertens, PhD, Department of Educational Foundations and Research, Gallaudet University “A powerful, richly nuanced, brilliantly innovative pedagogical intervention into the field of qualitative inquiry. This book is clearly written, grounded in case materials, and very accessible to students. The narrative is driven by the voices and insights of preeminent scholars, each an expert in one of five ways of doing qualitative analysis. This book represents the most innovative approach to date for teaching qualitative analysis. It will provide a starting place for the next generation of students who want to learn how to be well-grounded qualitative inquirers.”—Norman K. Denzin, PhD, College of Communications Scholar, University of Illinois at Urbana-Champaign

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Log In Home Around the Gulf Features and Columns News Shorts Search the Times Explore the Times About Us Recent News Call for Special Sessions for Coastal Zone Canada 2014 RFP for Climate Website Read Past Times Articles December 2013 Census of Marine Life exceeds expectations May 5, 2011Print“Imagine that you are the manager of a corporation. Now imagine that you know fewer than half the people who work for you and you have no idea what the other half does. In this situation, you can’t manage very well.” With this analogy, Lewis Incze, a biological oceanographer at the University of Maine and Principal Investigator for the Gulf of Maine Area (GoMA) program of the Census of Marine Life, described the situation facing those who would safeguard the world’s oceans and the motivation behind an audacious, 10-year long project to describe the inhabitants of marine environments around the globe. Figure 1: While the inventory of species in the Gulf of Maine area is far from complete, many key aspects of biodiversity are becoming better understood. Large conspicuous species, especially those of commercial importance, are best understood. Also, those organisms that live near the coast are better known than those in deep water offshore. Yet, research shows that lesser known species – including microscopic organisms – play critical roles in ecosystem functioning. (Photos, top to bottom: Peter Stevick, Jon Witman, Christine Kulfan, Linda Amaral Zettler) The Census of Marine Life (CoML), initiated by the Alfred P. Sloan Foundation in 2000, was designed to add to our knowledge of biodiversity in the world’s oceans. As the program drew to a close in 2010, most would agree that it had exceeded all expectations in its “decade of discovery.” Most of the projects within CoML focused on the deep ocean where sampling has been particularly deficient. 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Third, despite extensive knowledge about the Gulf, it is recognized that only a fraction of the regional biodiversity is known, and even less is understood about how this biodiversity contributes to the functioning and adaptability of the ecosystem. Figure 2. “How can we implement ecosystem-based management (EBM) under such conditions? What do we presently know about biodiversity, and what are some of the needs and useful strategies going forward? Research conducted by CoML could catalyze discussions and investments in answering these questions,” said Lawton. GoMA defined its study area as the Gulf of Maine proper (including the Bay of Fundy), Georges Bank and the Great South Channel, the western Scotian Shelf (south of a line extending from Halifax to the continental slope), the continual slope from the Halifax line to the Great South Channel, and Bear Seamount (on the deeper part of the slope south of Georges Bank). Extending the study beyond just the Gulf of Maine made it more comprehensive of regional oceanographic and biogeographic processes and built a stronger international effort between the U.S. and Canada. Graham Shimmield, former chair of the European branch of CoML and now Executive Director of the Bigelow Laboratory for Ocean Sciences in West Boothbay Harbor, Maine, described the impetus for the massive global research program as the need to “establish a baseline against which future change can be measured.” Noting that “70 percent of the global population lives within 50 miles of the coast,” Shimmield added “with more uses and more users, every part of the ocean is now affected by man…we have changed the whole ecology of the oceans by exploiting the resources that live there.” “The global ocean represents an asset of diminishing value… if we don’t master our understanding of the oceans and incorporate this into the way we manage our affairs, we should expect that this value will continue to diminish,” Incze said. “Our understanding of the oceans lags behind that of the terrestrial realm because it is harder to see and study. Ocean research is expensive, painstaking, and time consuming.” CoML was designed to give a boost to ocean researchers interested in biodiversity and “do for the oceans what terrestrial ecologists did for tropical rainforests a number of years ago,” Incze said. Importance of biodiversity Why is biodiversity important? A greater variety of genes (within-species diversity) and species helps to buffer ecosystems from the effects of environmental changes that are driven by natural processes and human activities. In a sense, biodiversity is a warehouse of response options. Biodiversity also delivers many important “ecosystem services” of value to people, from nutrient recycling to fish production and aesthetic enjoyment. Thus, conserving biodiversity at functional levels is one of the objectives of EBM. Researchers say some basic questions that need answers about the Gulf of Maine area are: 1) Who lives here (that is – what is the regional biodiversity)? 2) How is this diversity distributed (what are the patterns)? 3) What processes affect biodiversity – both positively and negatively? And 4) how does biodiversity affect the system? In other words, why does biodiversity matter to this area and what do we need to do to conserve it? There is an immense amount to learn, and one of the practical challenges is to devise research and management strategies that deliver on these important needs. The Gulf of Maine Area census worked with scientists and databases to assemble a list of more than 5,600 named species in the Gulf of Maine area, tripling the original estimate of what was known. And yet, it is estimated that thousands more species remain to be discovered and described (the estimate excludes bacteria, which are many times more diverse. (See Fig. 1) Figure 3. As a result of the census, an updated register of the named species will soon be available to researchers and any other interested people (see http://www.gulfofmaine-census.org, and http://www.marinebiodiversity.ca). The register is being developed so that species names are linked to other sources of information about the species (e.g., authoritative descriptions, ecology, life history) and to databases on their distributions in the Gulf of Maine and elsewhere around the world (see Ocean Biogeographic Information System: http://www.iobis.org). Rubber boots to ROVs Lawton described the work of the GoMA program as stretching across a range of scales of size and complexity and utilizing technology varying from “rubber boots to remotely operated vehicles (ROVs).” Work in Cobscook Bay, Maine, for example, incorporated detailed identification of life in the intertidal zone, while new acoustic technologies conducted unprecedented studies of herring schools the size of Manhattan Island. Other studies went beyond enumerating species to assessing the ecological role played by species and their physical habitat. Such studies have to focus on fairly small areas. Other projects looked at the full sweep of the Gulf. One combined data on 27 physical and oceanographic factors to assess environmental drivers of distribution patterns of organisms throughout the Gulf. A wide range of approaches to studying the Gulf is important because, as Incze and Lawton both emphasize, ecological structure is itself created by physical factors and biological processes operating at multiple scales. Lawton noted that the concept of “ecosystem services” provides “a framework where scientists and managers can work together to decide what information is needed, bridging the challenging gap between the curiosity-driven basic research at the heart of CoML and the very applied nature of most marine management issues. Managers often must focus on a given species, working to ensure that harvests are sustainable or that a threatened species is protected. Ecologists generally take a more holistic view, seeing each species as part of the larger ecosystem.” Ultimately, EBM requires that these two approaches get integrated. “Sustainable fish production is, after all, a by-product of a complex set of requirements and many interacting species, and the best way to ensure production into the future is to ensure that all the parts of the system (such as genes, species, and habitats) are able to function and respond naturally,” said Incze. In the meantime, the many legacies of the Census of Marine Life and its Gulf of Maine Area program will continue to help drive scientific discovery and management applications, said the scientists. Data generated by the program are now incorporated in the Ocean Biogeographic Information System, an online database, available to all as a place to find, store, and share data. Many research papers prepared by CoML scientists are available to anyone with an internet connection through the Public Library of Science, an organization committed to providing open access to research results. At a major conference held in London last October, scientists from around the world agreed that one of the greatest legacies of CoML is the teams of researchers that came together to tackle a wide range of research projects. CoML provided the opportunity to work across geographic, cultural, and institutional boundaries to invigorate research in marine biodiversity. The Gulf of Maine Area program was one of those showing how to lay the groundwork for productive collaborations – and effective input into management – well into the future. The Census of Marine Life: A Decade of Discovery 2,700 scientists 80+ nations 540 expeditions US$ 650 million by all nations 2,600+ scientific publications 6,000+ potential new species Side bar: Gulf of Maine Area Studied Area: 46,700 square miles New species discovered since 2000: 13 named; many collected that need further analysis Named species : >5,600 Species yet to be discovered: thousands Census of Marine Life: http://www.coml.org/ Gulf of Maine Area program of the Census of Marine Life: http://www.gulfofmaine-census.org/ Centre for Marine Biodiversity: http://www.marinebiodiversity.ca/ Ocean Biogeographic Information System: http://www.iobis.org/ Public Library of Science: http://www.plosone.org/ Related Gulf of Maine Times articles: What Lies Beneath: Exploring the Gulf of Maine Biodiversity Discovery Corridor (http://www.gulfofmaine.org/times/summer2007/biodiversity.html) Surprising Species Diversity Revealed (http://www.gulfofmaine.org/times/spring2006/species2.html) PrintTags: April/May 2011 Issue Support the Times Gulf of Maine Times Sponsors Copyright © 2014 Gulf of Maine Times. All Rights Reserved.

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ANZBY- OTCPK (USA)Australia and New Zealand Banking Group Limited Business Predictability Rank: 2-Star Back Testing Results:Average gain of all 2-Star stocks: 6% per year.% of Stocks that are in still loss if held for 10yrs: 16%.Read more: What is Predictability Rank?Performances of real portfolio ANZBY has been successfully added into Your Stock Email Alerts list. ANZBY has been removed from your Stock Email Alerts list. Australia and New Zealand Banking Group Limited (OTCPK:ANZBY) EV/EBITDA 24.45 (As of Today) EV/EBITDA ratio is calculated as enterprise value divided by its EBITDA. As of today, Australia and New Zealand Banking Group Limited's enterprise value is $205,767 Mil. Australia and New Zealand Banking Group Limited's earnings before depreciation and amortization for the trailing twelve months (TTM) ended in Sep. 2013 was $8,592 Mil. Therefore, Australia and New Zealand Banking Group Limited's EV/EBITDA ratio for today is 24.45. EV/EBITDA (Enterprise value/EBITDA) is a valuation multiple used in finance and investment to measure the value of a company. This important multiple is often used in conjunction with, or as an alternative to, the P/E Ratio to determine the fair market value of a company. As of today, Australia and New Zealand Banking Group Limited's stock price is $31.20. Australia and New Zealand Banking Group Limited's earnings per share for the trailing twelve months (TTM) ended in Sep. 2013 was $2.14. Therefore, Australia and New Zealand Banking Group Limited's P/E Ratio for today is 14.80. The "classic" EV/EBITDA ratio is much better in capturing debt and net cash than the P/E Ratio. Australia and New Zealand Banking Group Limited's EV/EBITDA for today is calculated as: EV/EBITDA=Enterprise Value (Today)/Earnings Before Depreciation and Amortization (TTM) =205767.383/8592.38095238 Australia and New Zealand Banking Group Limited's current Enterprise Value is $205,767 Mil. For company reported semi-annually, GuruFocus uses latest annual data as the TTM data. Australia and New Zealand Banking Group Limited's Earnings Before Depreciation and Amortization for the trailing twelve months (TTM) ended in Sep. 2013 was $8,592 Mil. Australia and New Zealand Banking Group Limited's P/E Ratio for today is calculated as: P/E Ratio=Share Price (Today)/Earnings Per Share (TTM) =31.20/2.13714285714 Australia and New Zealand Banking Group Limited's share price for today is $31.20. For company reported semi-annually, GuruFocus uses latest annual data as the TTM data. Australia and New Zealand Banking Group Limited's Earnings Per Share for the trailing twelve months (TTM) ended in Sep. 2013 was $2.14. Study has found that the companies with the lowest EV/EBITDA outperforms companies measured as cheap by other ratios such as P/E Ratio. Please read Which price ratio outperforms the enterprise multiple? Enterprise Value, Earnings Before Depreciation and Amortization, P/E Ratio Australia and New Zealand Banking Group Limited Annual Data ev2ebitda 20.1023.8022.4020.0523.6930.3221.4215.4417.1417.51 Australia and New Zealand Banking Group Limited Semi-Annual Data Mar09Sep09Mar10Sep10Mar11Sep11Mar12Sep12Mar13Sep13 0.0030.320.0021.420.0015.440.0017.140.0017.51 Financial Dictionary for Australia and New Zealand Banking Group Limited

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Colonials Athletics Weekend Preview - April 5-7 Five Programs Host Events, Gymnasts Compete at NCAA Regionals, Women's Water Polo and Sailing are on the Road GW baseball enters this weekend's three-game home series against Richmond tied for first in the Atlantic 10 at 5-1 in league play. BASEBALL - @GWBaseball1 Friday, 4 p.m.: Tickets | GameTracker | RaiseHigh.tv Saturday, 2 p.m.: Tickets | GameTracker | RaiseHigh.tv Sunday, 1 p.m.: Tickets | GameTracker | RaiseHigh.tv The George Washington baseball team, winners in seven of its last nine games, resumes its Atlantic 10 schedule by welcoming Richmond to Barcroft Park for a three-game series beginning on Friday at 4:00 p.m. GW (11-17, 5-1 A-10) scored four runs in the ninth inning to knock of George Mason, 11-9, on Tuesday in Fairfax, Va. Senior Tyler McCarthy roped a three-run double to send the Colonials to the win. McCarthy is batting a team-best .357 over the past 10 games with two doubles, two triples and four RBIs. Entering the weekend, GW is tied for first place in the conference with Saint Louis. The Colonials' pitching staff has a 1.17 ERA, 5-1 record and nearly a 3-to-1 strikeout-to-walk ratio in A-10 games this season. Junior Aaron Weisberg ranks seventh in the Atlantic 10 with a 2.37 ERA while classmate Craig Lejeune is tied for fourth with four saves. Richmond (18-9, 3-3 A-10) enters the weekend series with a 3-3 record, with a pair of wins over La Salle and a win against Charlotte. The Spiders rank fourth in the Atlantic 10 with a .282 team batting average and third in the conference with a 3.82 team ERA. Bret Williams is the Spiders' top offensive threat, ranking fourth in the conference with a .390 batting average along with six doubles and 20 RBIs. Richmond is 4-1 against common opponents they share with GW (2-0 vs. George Mason, 2-1 vs. Quinnipiac). SOFTBALL - @GW_Softball GW vs. Butler Game 1, Friday, 3 p.m. - GameTracker | RaiseHigh.tv GW vs. Butler Game 2, Saturday, 12 p.m. - GameTracker | RaiseHigh.tv GW vs. Saint Louis Game 1, Sunday, 12 p.m. - GameTracker | RaiseHigh.tv GW vs. Saint Louis Game 2, Sunday, 2 p.m. - GameTracker | RaiseHigh.tv The George Washington softball team returns home for the first time in two weeks to host four games in three days against Atlantic 10 rivals Butler and Saint Louis. The Colonials will host the Bulldogs on Friday at 3 p.m. and Saturday at 12 p.m., while the Billikens visit GW Softball Field for a doubleheader on Sunday beginning at 12 p.m. GW (11-17, 0-2 A-10) has dropped five in a row following Tuesday's 10-0 loss at Towson, but the Colonials are 9-6 at home and have won eight of their last 10 games played at GW Softball Field on the Mount Vernon Campus. Freshman first baseman Carlee Gray is batting a team-high .368 on the season. She has reached base in a school-record 18 consecutive games dating to Feb. 27 against Drexel, posting a .412 average and a .516 on-base percentage during the streak. Sophomore shortstop Victoria Valos is hitting .317 and leads the Colonials with 14 extra-base hits, 28 RBIs and 20 runs scored. Butler (11-16, 2-2 A-10) is 1-4 in its last five games, including a doubleheader sweep at the hands of Miami (Ohio) on Tuesday. In their first season in the Atlantic 10, the Bulldogs are led offensively by Kristen Boros, who is batting .333 with 12 extra-base hits, 16 RBIs and 11 runs scored. Jenny Esparza ranks second in the A-10 with a 1.47 ERA, and leads the league in opponent batting average, holding batters to a .136 clip at the plate. Saint Louis (14-14, 2-2 A-10) split a doubleheader with Eastern Illinois on Wednesday. The Billikens are batting just .209 as a team, led by shortstop Jessica Van Norstrand at .295. She also leads the Billikens with seven doubles, while catcher Alyson Brand and outfielder Lindsay Friedman have each driven in a team-high 15 runs. In addition, Saint Louis leads the league with 50 steals on the season, paced by outfielder Jessica Buschjost's A-10 leading 18 stolen bases. GW is 2-0 all-time against Butler, but the teams have not met since the 2007 Rebel Games in Kissimmee, Fla. The Colonials trail the Billikens, 10-5, in the all-time series after the teams' split last season's doubleheader in St. Louis. Senior Autumn Taylor is hitting .429 (6-for-14) all-time against SLU. She went 3-for-6 with a pair of stolen bases against the Billikens in 2012. LACROSSE - @GWLacrosse GW vs. La Salle, Friday, 4 p.m. - GameTracker | RaiseHigh.tv GW at #13 Massachusetts, Sunday, 1 p.m. - GameTracker | Watch Live The George Washington lacrosse team looks for to stay undefeated in Atlantic 10 action when it hosts La Salle on Friday at 4 p.m. at the GW Lacrosse Field on the Mount Vernon Campus, then travels to No. 13 Massachusetts for a 1 p.m. contest on Sunday. The Colonials (6-4, 1-0 A-10) are coming off a thrilling 11-10 win over Richmond on Friday in both teams' conference opener. Freshman Olivia Boudreau netted the game-winner with 1:52 remaining in regulation, and sophomore Allie Rash won the ensuing drawl control as GW maintained possession for the remainder of the game. The win was the first for the Colonials over the Spiders since 2008. Boudreau, who also scored the opening goal of the contest 2:11 into play, was named A-10 Rookie of the Week for the second time this year. She tallied her ninth and 10th goals of the season in the contest against Richmond, and along with her three assists, currently ranks fifth on the team and leads all freshmen with 13 points on the year. With 24 assists on the season, sophomore Jamie Bumgardner continues to rank atop the A-10. Her 24 helpers are also tied for 14th in NCAA Division I, while her 2.40 assists per game are good for 12th in the nation. Senior Nicole Lacey is tied for second in the A-10 with a 6.0 shots per game average. Already the Colonials' career and single-season draw controls leader, Lacey is also tied for second in the league with 3.20 draws per game. As a team, GW is tied for 12th in Division I and sits second in the conference with 19.0 ground balls per game, while sophomore Jenn Seitz is tied for third in the league with 2.40 ground balls per contest. On the defensive end, senior goalkeeper Jess Hicks is tied for third in the conference with 6.40 saves per game, and the Colonials are third with 8.70 caused turnovers per contest. La Salle (8-2, 0-1 A-10) comes to GW after dropping a 20-11 decision to Massachusetts on Saturday. Caitlyn Brostrand led the Explorers with three goals, and Alanna Diffendal, Kelly Furman and Melanie Sarcinello added two apiece as the 11 goals were the second-most scored on the Minutewomen this season. Brostrand (23g, 2a) and Lauren McDermott (19g, 5a) pace La Salle with 25 and 24 points, respectively. GW leads the all-time series with La Salle, 9-2, and has won five-straight over the Explorers. Last season, the Colonials earned an 8-7 victory on the road. Nationally ranked Massachusetts (9-2, 1-0 A-10) is currently riding a six-game winning streak dating back to March 2, and opened conference play on Saturday with a 20-11 win at La Salle. The Minutewomen have won 21 straight contests against A-10 opponents dating back to the 2010 season. Lauren Terracciano netted five goals in the squad's win over La Salle, while Cori Murray (3g, 3a) added six points and Sam Rush (4g, 1a) chipped in five points. Kelsey McGovern was named A-10 Defensive Player of the Week after winning 11 draw controls, picking up three ground balls and causing three turnovers against the Explorers. The Minutewomen lead the nation in scoring offense with a 16.09 goals-per-game average and rank among the top five in total points, scoring margin, caused turnovers and draw controls. UMass is paced on the season by Katie Ferris (31g, 14a) with 45 points, Murray (21g, 17a) with 38 points, Rush (33g, 4a) with 37 points and Terracciano (21g, 11a) with 32 points. MEN'S TENNIS - @GWMensTennis The No. 68 George Washington men's tennis team remains in Washington, D.C., for a pair of matches this weekend as it hosts St. John's on Saturday at 1 p.m. at the GW Tennis Center on the Mount Vernon Campus before heading to district foe Georgetown for an 11 a.m. match on Sunday. The Colonials' seniors, Leonardo Lapentti and Alexander van Gils, will be honored prior to Saturday's final home match. GW (10-5) picked up its third straight victory on Saturday in dominating fashion with a 6-1 win over local foe George Mason in the squad's outdoor home opener. In the first meeting between the two programs since 2002, the Colonials earned a doubles sweep before claiming victories at Nos. 1-5 singles. After going undefeated at No. 3 singles and No. 2 doubles in Saturday's match, freshman Danil Zelenkov was named the Atlantic 10 Rookie Performer of the Week for the second consecutive week and fourth time this spring - the most weekly awards for a men's tennis freshman in the league this season. Zelenkov is 10-4 in dual-match singles play, including 9-3 at the No. 3 position, and has been victorious in eight of his past nine matches. Junior Ulrik Thomsen leads the Buff and Blue with a 10-3 singles record this spring and has won eight of his last 10 matches, while classmate Nikita Fomin is 10-5 on the season and has won seven of his past eight outings. The 80th-ranked No. 3 doubles team of sophomore Francisco Dias and Lapentti extended its unbeaten streak to 10 with a win over GMU, and the pair has outscored its opponents by an 82-44 margin through finished competition. St. John's (2-12) first travels to Georgetown on Friday before making the short trip to GW. The Red Storm is currently in a two-match skid after falling to Penn (2-5) and Yale (2-5) the past two weekends. St. John's last victory was a 4-3 decision over Binghamton on March 17. Last season the Colonials fell to the Red Storm, 2-4, on the road. Georgetown (8-8) hosts St. John's and Fairfield on Friday and Saturday, respectively, before welcoming GW on Sunday morning. The Hoyas are currently riding a six-match winning streak dating back to March 15 and are coming off a 4-3 win at Villanova on Wednesday. Georgetown is led this spring by Casey Distaso, who owns an 11-2 dual-match singles mark, including undefeated records at the Nos. 4, 5 and 6 slots, and the No. 3 duo of Daniel Khanin and Reese Milner pace all doubles teams with an 8-2 record. Last season, GW downed Georgetown, 6-1, in its outdoor home opener. WOMEN'S TENNIS - @GW_Tennis The George Washington women's tennis team competes in a pair of non-conference matches this weekend as it welcomes East Carolina to the GW Tennis Center on the Mount Vernon Campus on Friday at 2:30 p.m. before traveling to James Madison on Saturday for a 1 p.m. match. Friday's contest will serve as the Colonials' Think Pink match in honor of breast cancer awareness. GW (9-5) looks to remain undefeated at home after knocking off Temple, 5-2, on Saturday. After earning the doubles point, the Colonials posted victories at the Nos. 1, 2, 4 and 6 singles spots to defeat the Owls for the first time since 2006. Three GW players own double-digit singles victories on the spring season: senior Mimi Hamling (11-3) and freshmen Lana Robins (10-4) and Stephanie Wei (10-4). Competing primarily at the No. 4 position, Hamling has won 11 of her past 13 matches, including nine straight from Feb. 1-March 12. Robins is currently on a two-match winning streak and has seen victories in six of her last eight matches, while Wei has won nine of her past 12 outings. East Carolina (11-7) split action last Friday, falling to UCF (1-6) before rebounding to defeat North Carolina Central (6-1). The Pirates are led by three players with double-digit singles victories, as Melis Tanik is 13-4 this spring, while Danielle Terpko and Neena Wanko are both 10-8. ECU first travels to Atlantic 10 foe Richmond on Thursday afternoon before making the trip to GW. The match between the Colonials and the Pirates will be the first in ninth-year head coach Dawn Buth's tenure. James Madison (7-5) welcomes GW as it wraps a four-match homestand. The Dukes most recently fell to Liberty, 3-4, on Tuesday, snapping a five-match winning streak. JMU is led this season by Katherine Bulling (9-2) and Cara Wirth (8-2). The Colonials look to avenge a 6-1 home loss to the Dukes during the 2011 season. GYMNASTICS - @GWGymnastics NCAA Regional Central | Live Stats | FREE Video Senior Stephanie Stoicovy and juniors Betsy Zander and Taylor Henderson will compete in the NCAA Southeast Regional at the Stephen C. O'Connell Center at the University of Florida this weekend as individual performers. Stoicovy and Zander each qualified as all-around performers while Henderson earned a bid as an uneven bars event specialist. Also earning bids as event specialist alternates were junior Kiera Kenney (uneven bars), sophomore Elena Corcoran (vault) and seniors Kayla Carto (balance beam) and Nefertiti Roy (floor exercise). The top two teams and the top two all-around competitors (who are not on an advancing team) from each regional will receive an automatic berth to the NCAA national championships hosted by UCLA in Los Angeles, Calif., April 19-21. In addition, the event winners at each regional site will advance to the national championships (in that event only) if they are not part of a qualifying team or an all-around qualifier. Stoicovy finished the season with a RQS of 39.060 in the all-around. The Erie, Pa., native finished tied for second on the floor exercise at the East Atlantic Gymnastics League (EAGL) Championship on March 23. Stoicovy was named to the All-EAGL First Team for the floor exercise and all-around following her impressive senior season. Zander finished tied for second place in the all-around at the EAGL Championship, tying her career-high score with a 39.150. She earned All-EAGL First Team honors on the all-around and a Second Team nod on the balance beam. Henderson earned All-EAGL Second Team honors on the uneven bars, after leading the Colonials on the event throughout the season. Her RQS of 9.795 tied her for 10th in the EAGL. WOMEN'S WATER POLO - @GW_WaterPolo In its final tune-up before the Collegiate Water Polo Association (CWPA) Southern Division Championship, the George Washington women's water polo team heads to Princeton, N.J., on Saturday to take on Southern Division rival Harvard at 12 p.m. and non-conference foe VMI at 4 p.m. at Princeton's DeNunzio Pool. GW (12-11, 2-2 Southern) has not played since a 9-8 win over Villanova on March 23. Junior Rachael Bentley leads the Colonials with 49 assists and 82 points, and her 49 assists are just one shy of the school record of 50, which she set last season. In addition, she has become the Colonials' all-time assists leader with 129, and ranks third all-time at GW with 243 career points, just 10 behind all-time leader Vanessa Fravel's 253 set from 2001-04. Freshman Hannah Cox paces GW with 54 goals and 31 ejections drawn. Cox's 54 goals are tied with Heather Walenga ('00) for the third-most in a single season in school history. Kira Cannon set the record at 71 in 2003. Harvard (13-10, 2-1 A-10) has dropped six in a row and is coming off a 12-10 loss to Southern Division rival Brown on Wednesday. Aisha Price leads the Crimson with 51 goals, 32 assists and 48 steals on the season. Goalie Ariel Dukes has recorded 176 saves in the cage for Harvard. In just its second season as a varsity program, VMI (11-14) has lost five of its last seven games, including a pair of defeats at the hands of MAAC rivals Wagner and Villanova on March 30. Celine Lazzaro leads the Keydets with 71 goals on the year, and goalie Molly Watkins has recorded 208 saves. The Crimson defeated the Colonials, 18-12, last season at the Charles E. Smith Center Pool. Katherine Berry led the Colonials with six points on four goals and two assists in that contest. GW defeated VMI, 19-7, last season in the first-ever matchup between the two teams. Megan Brolley tallied seven points on four goals and three helpers to lead GW in the game. SAILING - @GW_Sailing GW sailing will send a young corps of sailors to the Greater New York Dinghy Regatta hosted by Fordham and Columbia in Bronx, N.Y., this weekend. Head coach John Pearce will send freshmen Jay Spector and Henry Young to compete in A Division, and freshman Benjamin Helfand, sophomore Jennifer Wilson, and senior heavy-air crew Sloan Dickey in B Division to the event in Eastchester Bay. The quintet will be part of an 18-team field consisting of the host Rams and Lions, as well as Army, Brown, Connecticut College, Cornell, Fairfield, Merchant Marine, Middlebury, Maritime, Old Dominion, Princeton, Syracuse, Penn, Rhode Island, Villanova and Wesleyan. "We have a very strong freshman class that has really stepped up as team leaders this year, so it's great for this group to get more regatta experience and prepare for a bright future," said Coach Pearce. Athletics News Home

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HackCollege Work Smarter, Not Harder HOME>>Top 12 Colleges for Undergraduates in 2012 Top 12 Colleges for Undergraduates in 2012 Posted 1/14/13 in @hackcollege.com, lists, newsworthy 0 Comments and 0 Reactions While most colleges and universities gain notoriety through the strength of their graduate-level programs, the majority of college students in the U.S. never advance beyond a four-year degree, making it often hard to judge which institutions are best for those on the undergraduate level. To help students gauge which universities are the best for attaining an undergraduate degree, the U.S. News & World report conducts a survey of college administrators every spring that ranks the top U.S. universities in undergraduate programs. Here’s the list of the top 12 national universities for undergraduates in 2012: Founded in 1769, Dartmouth is a private, Ivy League institution that is home to some impressive liberal arts programs as well as numerous prestigious postgraduate programs. Princeton University Princeton is unique among Ivy League research universities due to its stated, unflagging commitment to undergraduate studies. Miami University–Oxford Oxford, OH The 10th oldest public university in the U.S., Mixami University has routinely shown its commitment towards providing an Ivy League-style education for as many students as possible, currently housing over 20,000 students system-wide. Taking only 8.9% of all undergraduate applications each year, Brown is one of the world’s most selective undergraduate institutions. But their exclusivity also allows for smaller class sizes and a greater investment in those students who make it in. Originally founded to train clergy in 1718, Yale is the third oldest university in the United States and has since become one of the best funded universities on the planet and has been the alma mater of five U.S. presidents. The second oldest university in the United States, William and Mary spent its firs 300 years as a private institution before becoming public in 1905. Since then, it maintains intimate class sizes in order to provide personalized experiences for its undergraduates. University of Michigan–Ann Arbor One of the founding members of the Association of American Universities, University of Michigan prides itself on being one of eight “Public Ivy” institutions, and provides world-class education to 40,000 students across its undergraduate and graduate programs. While famous for its athletic programs, Duke has a campus that spans over 8,600 acres and ranks 35th in the world for academic excellence. University of California–Berkeley Berkley, CA Offering over 350 undergraduate degrees, the UofC at Berkely is the oldest campus of the ten major campuses of the University of California, and through its mission to provide both “classical and practical” education to its undergrads, it also stands out as the University of California’s flagship institution. While primarily serving postgraduate students and its massive $423.7 million research budget, the University of Chicago is also known for instilling strong critical thinking and interdisciplinary practices in its undergraduate students. The University of Chicago is also affiliated with 87 Nobel Laureates. University of Maryland–Baltimore County With a strong emphasis on teaching the natural sciences, information technology, engineering, human services, and public policy on the undergraduate level since the late 60′s, few universities better prepare students for the current job market than this. Notre Dame, IN Although famously known as one of the largest Catholic research universities in the country, Notre Dame prides itself on championing social issues and hosts one of the largest female populations of any university. Tyler Mangrum is a writer based out of Seattle, Washington, and is currently the News Editor for HackCollege.com. His articles have been published on sites like Forbes and the Huffington Post. In his free time, he enjoys video games, ardently defending the Oxford comma, and avoiding sunlight at all costs. You cannot follow him on Twitter, because he thinks that’s kinda weird. prev Over 300 College Presidents Aim to Ban Guns on Campuses, Reform Gun Laws next How To Handle Your Health Tags: lists, newsworthy How to Create Structure in College with a Calendar and To-Do List College is undeniably one of the best experiences in a young person's life. New friends, new freedoms, and a new start all contribute to this overwhelming beginning. With all the new doors to be opened, however, it becomes hard to stay on top of what’s important at school. I’m not simply spea... 8 Great Food Hacks For Healthier Eating Eating healthy doesn’t always have to be quite as time consuming as it seems. Sure, it takes a hot second to squeeze a lemon or chop fresh vegetables, but we’ve got a handful of food hacks that will help you save time and money when trying to develop better eating habits! They might not all wor... 8 Pros and Cons of Living On Campus in College Whether you are living on campus now or thinking of going back, you know there are some serious downsides to living in university-owned housing. Personally, I feel every student should live on campus at least one year (the first year typically works best). We’ll get into the benefits of it late... Hack College's School Directory There are millions of things in the world to study. Let us help you narrow it down. Here's a sneak peak at a few of our subjects below! Organizational Psychology Schools School Psychology Schools There are many places to study. Let us help you narrow it down. Here's a sneak peak at US states below. Schools in Alabama Schools in California State & Subject There are many places to study. Let us help you narrow it down. Here's a sneak peak at subjects in US states below. Organizational Psychology Schools in Alabama Culinary Schools in California School Psychology Schools in California City & Subject There are many places to study. Let us help you narrow it down. Here's a sneak peak at subjects in US cities below. Organizational Psychology Schools in Eight Mile, AL Organizational Psychology Schools in Huntsville, AL Organizational Psychology Schools in Normal, AL Culinary Schools in Alta Loma, CA Culinary Schools in Clovis, CA Culinary Schools in Costa Mesa, CA School Psychology Schools in Encino, CA School Psychology Schools in Fresno, CA School Psychology Schools in Irvine, CA School Psychology Schools in La Jolla, CA School Psychology Schools in La Verne, CA School Psychology Schools in Los Angeles, CA Culinary Schools in Marysville, CA School Psychology Schools in Orange, CA School Psychology Schools in Riverside, CA Culinary Schools in San Bernardino, CA School Psychology Schools in San Diego, CA School Psychology Schools in Stockton, CA Culinary Schools in Wilmington, CA Search our entire school directory below And / Or © 2006-2014 HackCollege. All Rights Reserved Privacy Policy

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