Question: What ctenophore was accidentally introduced into The Black Sea?

Answer: Mnemiopsis

Ctenophores may be abundant during the summer months in some coastal locations, but in other places they are uncommon and difficult to find. In bays where they occur in very high numbers, predation by ctenophores may control the populations of small zooplanktonic organisms such as copepods, which might otherwise wipe out the phytoplankton (planktonic plants), which are a vital part of marine food chains. <hl> One ctenophore, Mnemiopsis , has accidentally been introduced into the Black Sea, where it is blamed for causing fish stocks to collapse by eating both fish larvae and organisms that would otherwise have fed the fish. <hl> The situation was aggravated by other factors, such as over-fishing and long-term environmental changes that promoted the growth of the Mnemiopsis population. The later accidental introduction of Beroe helped to mitigate the problem, as Beroe preys on other ctenophores.

Ctenophores may be abundant during the summer months in some coastal locations, but in other places they are uncommon and difficult to find. In bays where they occur in very high numbers, predation by ctenophores may control the populations of small zooplanktonic organisms such as copepods, which might otherwise wipe out the phytoplankton (planktonic plants), which are a vital part of marine food chains. One ctenophore, <hl> Mnemiopsis <hl>, has accidentally been introduced into the Black Sea, where it is blamed for causing fish stocks to collapse by eating both fish larvae and organisms that would otherwise have fed the fish. The situation was aggravated by other factors, such as over-fishing and long-term environmental changes that promoted the growth of the Mnemiopsis population. The later accidental introduction of Beroe helped to mitigate the problem, as Beroe preys on other ctenophores.

One ctenophore, <hl> Mnemiopsis <hl> , has accidentally been introduced into the Black Sea, where it is blamed for causing fish stocks to collapse by eating both fish larvae and organisms that would otherwise have fed the fish.


Question: What event was blamed on the introduction of mnemiopsis into The Black Sea?

Ctenophores may be abundant during the summer months in some coastal locations, but in other places they are uncommon and difficult to find. In bays where they occur in very high numbers, predation by ctenophores may control the populations of small zooplanktonic organisms such as copepods, which might otherwise wipe out the phytoplankton (planktonic plants), which are a vital part of marine food chains. One ctenophore, Mnemiopsis, has accidentally been introduced into the Black Sea, where it is blamed for causing fish stocks to collapse by eating both fish larvae and organisms that would otherwise have fed the fish. The situation was aggravated by other factors, such as over-fishing and long-term environmental changes that promoted the growth of the Mnemiopsis population. The later accidental introduction of Beroe helped to mitigate the problem, as Beroe preys on other ctenophores.

Answer: causing fish stocks to collapse

Ctenophores may be abundant during the summer months in some coastal locations, but in other places they are uncommon and difficult to find. In bays where they occur in very high numbers, predation by ctenophores may control the populations of small zooplanktonic organisms such as copepods, which might otherwise wipe out the phytoplankton (planktonic plants), which are a vital part of marine food chains. <hl> One ctenophore, Mnemiopsis, has accidentally been introduced into the Black Sea, where it is blamed for causing fish stocks to collapse by eating both fish larvae and organisms that would otherwise have fed the fish. <hl> The situation was aggravated by other factors, such as over-fishing and long-term environmental changes that promoted the growth of the Mnemiopsis population. The later accidental introduction of Beroe helped to mitigate the problem, as Beroe preys on other ctenophores.

Ctenophores may be abundant during the summer months in some coastal locations, but in other places they are uncommon and difficult to find. In bays where they occur in very high numbers, predation by ctenophores may control the populations of small zooplanktonic organisms such as copepods, which might otherwise wipe out the phytoplankton (planktonic plants), which are a vital part of marine food chains. One ctenophore, Mnemiopsis, has accidentally been introduced into the Black Sea, where it is blamed for <hl> causing fish stocks to collapse <hl> by eating both fish larvae and organisms that would otherwise have fed the fish. The situation was aggravated by other factors, such as over-fishing and long-term environmental changes that promoted the growth of the Mnemiopsis population. The later accidental introduction of Beroe helped to mitigate the problem, as Beroe preys on other ctenophores.


Question: What was done to counteract the overpopulation of mnemiopsis in The Black Sea?

Answer: introduction of Beroe

Ctenophores may be abundant during the summer months in some coastal locations, but in other places they are uncommon and difficult to find. In bays where they occur in very high numbers, predation by ctenophores may control the populations of small zooplanktonic organisms such as copepods, which might otherwise wipe out the phytoplankton (planktonic plants), which are a vital part of marine food chains. One ctenophore, Mnemiopsis, has accidentally been introduced into the Black Sea, where it is blamed for causing fish stocks to collapse by eating both fish larvae and organisms that would otherwise have fed the fish. The situation was aggravated by other factors, such as over-fishing and long-term environmental changes that promoted the growth of the Mnemiopsis population. <hl> The later accidental introduction of Beroe helped to mitigate the problem, as Beroe preys on other ctenophores. <hl>

Ctenophores may be abundant during the summer months in some coastal locations, but in other places they are uncommon and difficult to find. In bays where they occur in very high numbers, predation by ctenophores may control the populations of small zooplanktonic organisms such as copepods, which might otherwise wipe out the phytoplankton (planktonic plants), which are a vital part of marine food chains. One ctenophore, Mnemiopsis, has accidentally been introduced into the Black Sea, where it is blamed for causing fish stocks to collapse by eating both fish larvae and organisms that would otherwise have fed the fish. The situation was aggravated by other factors, such as over-fishing and long-term environmental changes that promoted the growth of the Mnemiopsis population. The later accidental <hl> introduction of Beroe <hl> helped to mitigate the problem, as Beroe preys on other ctenophores.


Question: When did the Cretaceous-Paleogene extinction happen?

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Answer: 66 million years ago

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. <hl> A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago . <hl> Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event <hl> 66 million years ago <hl>. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event <hl> 66 million years ago <hl> .


Question: Evidence indicates that Cydippids are not what?

Answer: monophyletic

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. <hl> Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic , in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids. <hl>

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not <hl> monophyletic <hl>, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Evidence accumulating since the 1980s indicates that the "cydippids" are not <hl> monophyletic <hl> , in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.


Question: How old are the fossils found that represent ctenophhores ?

Answer: 515 million years

<hl> Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. <hl> The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about <hl> 515 million years <hl> ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.


Question: What were the fossils that were found to represent ctenphores missing that current ctenphora have?

Answer: tentacles

<hl> Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. <hl> The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no <hl> tentacles <hl> but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.


Question: Fossils found that were believed to be ctenophores were how old?

Answer: 515 million years

<hl> Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. <hl> The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about <hl> 515 million years <hl> ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.


Question: What event happened 66 million years ago?

Answer: Cretaceous–Paleogene extinction

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. <hl> A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. <hl> Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the <hl> Cretaceous–Paleogene extinction <hl> event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.


Question: Cypiddids are not what?

Answer: monophyletic

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. <hl> Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic , in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids. <hl>

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not <hl> monophyletic <hl>, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Evidence accumulating since the 1980s indicates that the "cydippids" are not <hl> monophyletic <hl> , in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.


Question: What do current ctenophores have that fossils found did not have?

Answer: tentacles

<hl> Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. <hl> The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no <hl> tentacles <hl> but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 515 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous–Paleogene extinction event 66 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.


Question: Jellyfish ans sea anemones belong to what phylum?

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.

Answer: cnidarians

<hl> Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). <hl> Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores form an animal phylum that is more complex than sponges, about as complex as <hl> cnidarians <hl> (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: What makes ctenophores different from all other animals?

Answer: by having colloblasts

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. <hl> Ctenophores are distinguished from all other animals by having colloblasts , which are sticky and adhere to prey, although a few ctenophore species lack them. <hl>

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals <hl> by having colloblasts <hl>, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores are distinguished from all other animals <hl> by having colloblasts <hl> , which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: Ctenophora are less complex than which other phylum?

Answer: bilaterians

<hl> Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). <hl> Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than <hl> bilaterians <hl> (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: Which phylum is more complex than sponges?

Answer: Ctenophores

<hl> Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). <hl> Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.

<hl> Ctenophores <hl> form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: What does ctenophore use to capture prey?

Answer: colloblasts

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. <hl> Ctenophores are distinguished from all other animals by having colloblasts , which are sticky and adhere to prey, although a few ctenophore species lack them. <hl>

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having <hl> colloblasts <hl>, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores are distinguished from all other animals by having <hl> colloblasts <hl> , which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: Jellyfish and sea anemones belong to which group/

Answer: cnidarians

<hl> Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). <hl> Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores form an animal phylum that is more complex than sponges, about as complex as <hl> cnidarians <hl> (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: What do ctenophores have that no other animals have?

Answer: colloblasts

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. <hl> Ctenophores are distinguished from all other animals by having colloblasts , which are sticky and adhere to prey, although a few ctenophore species lack them. <hl>

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having <hl> colloblasts <hl>, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores are distinguished from all other animals by having <hl> colloblasts <hl> , which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: What do ctenophore use to capture their prey?

Answer: colloblasts

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. <hl> Ctenophores are distinguished from all other animals by having colloblasts , which are sticky and adhere to prey, although a few ctenophore species lack them. <hl>

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having <hl> colloblasts <hl>, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores are distinguished from all other animals by having <hl> colloblasts <hl> , which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: Which two groups have cells bound by inter-cell connections and membranes, muscles, a nervous system and sensory organs?

Answer: ctenophores and cnidarians

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). <hl> Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. <hl> Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). Unlike sponges, both <hl> ctenophores and cnidarians <hl> have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: Ctenophores are less complex than what other group?

Answer: bilaterians

<hl> Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians (which include almost all other animals). <hl> Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than <hl> bilaterians <hl> (which include almost all other animals). Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts, which are sticky and adhere to prey, although a few ctenophore species lack them.


Question: What is the jelly-like susbtance called?

Like sponges and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. Hence ctenophores and cnidarians have traditionally been labelled diploblastic, along with sponges. Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.

Answer: mesoglea

<hl> Like sponges and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. <hl> Hence ctenophores and cnidarians have traditionally been labelled diploblastic, along with sponges. Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.

Like sponges and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the <hl> mesoglea <hl> in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. Hence ctenophores and cnidarians have traditionally been labelled diploblastic, along with sponges. Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.


Question: Ctenophores and cnidarians are classified as what?

Answer: diploblastic

Like sponges and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. <hl> Hence ctenophores and cnidarians have traditionally been labelled diploblastic , along with sponges. <hl> Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.

Like sponges and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. Hence ctenophores and cnidarians have traditionally been labelled <hl> diploblastic <hl>, along with sponges. Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.

Hence ctenophores and cnidarians have traditionally been labelled <hl> diploblastic <hl> , along with sponges.


Question: Which group has two layers of cells with a middle layer of mesoglea?

Answer: sponges and cnidarians, ctenophores

<hl> Like sponges and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. <hl> Hence ctenophores and cnidarians have traditionally been labelled diploblastic, along with sponges. Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.

Like <hl> sponges and cnidarians, ctenophores <hl> have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. Hence ctenophores and cnidarians have traditionally been labelled diploblastic, along with sponges. Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.


Question: Ctenophores, cnidarians and what other group are labelled diploblastic?

Answer: sponges

<hl> Like sponges and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. <hl> Hence ctenophores and cnidarians have traditionally been labelled diploblastic, along with sponges. Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.

Like <hl> sponges <hl> and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. Hence ctenophores and cnidarians have traditionally been labelled diploblastic, along with sponges. Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer, and as a result some recent text books classify ctenophores as triploblastic, while others still regard them as diploblastic.


Question: What are the hairs on ctenophores called?

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main method of locomotion. Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "ctenes," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. The name "ctenophora" means "comb-bearing", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".

Answer: cilia

<hl> Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main method of locomotion. <hl> Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "ctenes," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. The name "ctenophora" means "comb-bearing", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use <hl> cilia <hl> ("hairs") as their main method of locomotion. Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "ctenes," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. The name "ctenophora" means "comb-bearing", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".


Question: What are cilia used for?

Answer: method of locomotion

<hl> Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main method of locomotion . <hl> Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "ctenes," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. The name "ctenophora" means "comb-bearing", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main <hl> method of locomotion <hl>. Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "ctenes," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. The name "ctenophora" means "comb-bearing", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main <hl> method of locomotion <hl> .


Question: Comb like bands of cilia are called what?

Answer: ctenes

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main method of locomotion. <hl> Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called " ctenes ," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. <hl> The name "ctenophora" means "comb-bearing", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main method of locomotion. Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "<hl> ctenes <hl>," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. The name "ctenophora" means "comb-bearing", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".

Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called " <hl> ctenes <hl> ," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below.


Question: What does ctenophore mean in Greek?

Answer: comb-bearing

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main method of locomotion. Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "ctenes," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. <hl> The name "ctenophora" means " comb-bearing ", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying". <hl>

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size, ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main method of locomotion. Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "ctenes," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below. The name "ctenophora" means "<hl> comb-bearing <hl>", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".

The name "ctenophora" means " <hl> comb-bearing <hl> ", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".


Question: Which cidippid is used as a description on ctenophores in most textbooks?

For a phylum with relatively few species, ctenophores have a wide range of body plans. Coastal species need to be tough enough to withstand waves and swirling sediment particles, while some oceanic species are so fragile that it is very difficult to capture them intact for study. In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. Hence most attention has until recently concentrated on three coastal genera – Pleurobrachia, Beroe and Mnemiopsis. At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.

Answer: Pleurobrachia

For a phylum with relatively few species, ctenophores have a wide range of body plans. Coastal species need to be tough enough to withstand waves and swirling sediment particles, while some oceanic species are so fragile that it is very difficult to capture them intact for study. In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. <hl> Hence most attention has until recently concentrated on three coastal genera – Pleurobrachia , Beroe and Mnemiopsis. <hl> At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.

For a phylum with relatively few species, ctenophores have a wide range of body plans. Coastal species need to be tough enough to withstand waves and swirling sediment particles, while some oceanic species are so fragile that it is very difficult to capture them intact for study. In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. Hence most attention has until recently concentrated on three coastal genera – <hl> Pleurobrachia <hl>, Beroe and Mnemiopsis. At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.

Hence most attention has until recently concentrated on three coastal genera – <hl> Pleurobrachia <hl> , Beroe and Mnemiopsis.


Question: Which group of ctenophore are are hardest to study?

Answer: oceanic species

For a phylum with relatively few species, ctenophores have a wide range of body plans. <hl> Coastal species need to be tough enough to withstand waves and swirling sediment particles, while some oceanic species are so fragile that it is very difficult to capture them intact for study. <hl> In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. Hence most attention has until recently concentrated on three coastal genera – Pleurobrachia, Beroe and Mnemiopsis. At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.

For a phylum with relatively few species, ctenophores have a wide range of body plans. Coastal species need to be tough enough to withstand waves and swirling sediment particles, while some <hl> oceanic species <hl> are so fragile that it is very difficult to capture them intact for study. In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. Hence most attention has until recently concentrated on three coastal genera – Pleurobrachia, Beroe and Mnemiopsis. At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.


Question: Why are coastal species tough?

Answer: to withstand waves and swirling sediment particles

For a phylum with relatively few species, ctenophores have a wide range of body plans. <hl> Coastal species need to be tough enough to withstand waves and swirling sediment particles , while some oceanic species are so fragile that it is very difficult to capture them intact for study. <hl> In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. Hence most attention has until recently concentrated on three coastal genera – Pleurobrachia, Beroe and Mnemiopsis. At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.

For a phylum with relatively few species, ctenophores have a wide range of body plans. Coastal species need to be tough enough <hl> to withstand waves and swirling sediment particles <hl>, while some oceanic species are so fragile that it is very difficult to capture them intact for study. In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. Hence most attention has until recently concentrated on three coastal genera – Pleurobrachia, Beroe and Mnemiopsis. At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.

Coastal species need to be tough enough <hl> to withstand waves and swirling sediment particles <hl> , while some oceanic species are so fragile that it is very difficult to capture them intact for study.


Question: Which ctenophora have been studies the most?

Answer: Pleurobrachia, Beroe and Mnemiopsis

For a phylum with relatively few species, ctenophores have a wide range of body plans. Coastal species need to be tough enough to withstand waves and swirling sediment particles, while some oceanic species are so fragile that it is very difficult to capture them intact for study. In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. <hl> Hence most attention has until recently concentrated on three coastal genera – Pleurobrachia, Beroe and Mnemiopsis . <hl> At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.

For a phylum with relatively few species, ctenophores have a wide range of body plans. Coastal species need to be tough enough to withstand waves and swirling sediment particles, while some oceanic species are so fragile that it is very difficult to capture them intact for study. In addition oceanic species do not preserve well, and are known mainly from photographs and from observers' notes. Hence most attention has until recently concentrated on three coastal genera – <hl> Pleurobrachia, Beroe and Mnemiopsis <hl>. At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.

Hence most attention has until recently concentrated on three coastal genera – <hl> Pleurobrachia, Beroe and Mnemiopsis <hl> .


Question: The inside of a ctenophore is lined with what?

The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.

Answer: epithelium

The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. <hl> The inner surface of the cavity is lined with an epithelium , the gastrodermis. <hl> The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.

The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an <hl> epithelium <hl>, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.

The inner surface of the cavity is lined with an <hl> epithelium <hl> , the gastrodermis.


Question: What do photocytes produce?

Answer: bioluminescence

The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. <hl> The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence . <hl> The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.

The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce <hl> bioluminescence <hl>. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.

The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce <hl> bioluminescence <hl> .


Question: What is the throat called?

Answer: pharynx

<hl> The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. <hl> These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.

The internal cavity forms: a mouth that can usually be closed by muscles; a <hl> pharynx <hl> ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.


Question: What does the internal cavity contain?

Answer: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals.

<hl> The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. <hl> The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.

The internal cavity forms: <hl> a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. <hl> These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.


Question: What are the most active parts of ctenophora?

Answer: the mouth and pharynx;

The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. <hl> These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. <hl> The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.

The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: <hl> the mouth and pharynx; <hl> the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.


Question: What are the eight comb rows on the outer surface called?

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

Answer: swimming-plates

<hl> The outer surface bears usually eight comb rows, called swimming-plates , which are used for swimming. <hl> The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

The outer surface bears usually eight comb rows, called <hl> swimming-plates <hl>, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

The outer surface bears usually eight comb rows, called <hl> swimming-plates <hl> , which are used for swimming.


Question: Combs are called what?

Answer: also called "ctenes" or "comb plates

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. <hl> The "combs" ( also called "ctenes" or "comb plates ") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). <hl> Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (<hl> also called "ctenes" or "comb plates <hl>") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

The "combs" ( <hl> also called "ctenes" or "comb plates <hl> ") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in).


Question: What does the 9 +3 pattern of cilia thought to do?

Answer: supporting function

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). <hl> Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function . <hl> These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a <hl> supporting function <hl>. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a <hl> supporting function <hl> .


Question: What direction do ctenophore swim?

Answer: in the direction in which the mouth is pointing,

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. <hl> Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. <hl> When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in). Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim <hl> in the direction in which the mouth is pointing, <hl> unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.


Question: Cilia can g ow up too what length?

Answer: 2 millimeters (0.079 in)

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. <hl> The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to 2 millimeters (0.079 in) . <hl> Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

The outer surface bears usually eight comb rows, called swimming-plates, which are used for swimming. The rows are oriented to run from near the mouth (the "oral pole") to the opposite end (the "aboral pole"), and are spaced more or less evenly around the body, although spacing patterns vary by species and in most species the comb rows extend only part of the distance from the aboral pole towards the mouth. The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to <hl> 2 millimeters (0.079 in) <hl>. Unlike conventional cilia and flagella, which has a filament structure arranged in a 9 + 2 pattern, these cilia are arranged in a 9 + 3 pattern, where the extra compact filament is suspected to have a supporting function. These normally beat so that the propulsion stroke is away from the mouth, although they can also reverse direction. Hence ctenophores usually swim in the direction in which the mouth is pointing, unlike jellyfish. When trying to escape predators, one species can accelerate to six times its normal speed; some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

The "combs" (also called "ctenes" or "comb plates") run across each row, and each consists of thousands of unusually long cilia, up to <hl> 2 millimeters (0.079 in) <hl> .


Question: How do ctenophores control buoyancy?

It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on osmotic pressure to adapt to water of different densities. Their body fluids are normally as concentrated as seawater. If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to increase its bulk and decrease its density, to avoid sinking. Conversely if they move from brackish to full-strength seawater, the rosettes may pump water out of the mesoglea to reduce its volume and increase its density.

Answer: osmotic pressure

<hl> It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on osmotic pressure to adapt to water of different densities. <hl> Their body fluids are normally as concentrated as seawater. If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to increase its bulk and decrease its density, to avoid sinking. Conversely if they move from brackish to full-strength seawater, the rosettes may pump water out of the mesoglea to reduce its volume and increase its density.

It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on <hl> osmotic pressure <hl> to adapt to water of different densities. Their body fluids are normally as concentrated as seawater. If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to increase its bulk and decrease its density, to avoid sinking. Conversely if they move from brackish to full-strength seawater, the rosettes may pump water out of the mesoglea to reduce its volume and increase its density.


Question: Ciliary rosettes pump water into what to control buoyancy?

Answer: the mesoglea

It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on osmotic pressure to adapt to water of different densities. Their body fluids are normally as concentrated as seawater. <hl> If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to increase its bulk and decrease its density, to avoid sinking. <hl> Conversely if they move from brackish to full-strength seawater, the rosettes may pump water out of the mesoglea to reduce its volume and increase its density.

It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on osmotic pressure to adapt to water of different densities. Their body fluids are normally as concentrated as seawater. If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into <hl> the mesoglea <hl> to increase its bulk and decrease its density, to avoid sinking. Conversely if they move from brackish to full-strength seawater, the rosettes may pump water out of the mesoglea to reduce its volume and increase its density.


Question: What does pumping water into the mesoglea do?

Answer: increase its bulk and decrease its density

It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on osmotic pressure to adapt to water of different densities. Their body fluids are normally as concentrated as seawater. <hl> If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to increase its bulk and decrease its density , to avoid sinking. <hl> Conversely if they move from brackish to full-strength seawater, the rosettes may pump water out of the mesoglea to reduce its volume and increase its density.

It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on osmotic pressure to adapt to water of different densities. Their body fluids are normally as concentrated as seawater. If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to <hl> increase its bulk and decrease its density <hl>, to avoid sinking. Conversely if they move from brackish to full-strength seawater, the rosettes may pump water out of the mesoglea to reduce its volume and increase its density.

If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to <hl> increase its bulk and decrease its density <hl> , to avoid sinking.


Question: What does the ciliary rosettes do to decease bulk and increase density?

Answer: pump water out of the mesoglea

It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on osmotic pressure to adapt to water of different densities. Their body fluids are normally as concentrated as seawater. If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to increase its bulk and decrease its density, to avoid sinking. Conversely if they move from brackish to full-strength seawater, <hl> the rosettes may pump water out of the mesoglea to reduce its volume and increase its density. <hl>

It is uncertain how ctenophores control their buoyancy, but experiments have shown that some species rely on osmotic pressure to adapt to water of different densities. Their body fluids are normally as concentrated as seawater. If they enter less dense brackish water, the ciliary rosettes in the body cavity may pump this into the mesoglea to increase its bulk and decrease its density, to avoid sinking. Conversely if they move from brackish to full-strength seawater, the rosettes may <hl> pump water out of the mesoglea <hl> to reduce its volume and increase its density.


Question: What is the largest sensory feature of the ctenophora?

The largest single sensory feature is the aboral organ (at the opposite end from the mouth). Its main component is a statocyst, a balance sensor consisting of a statolith, a solid particle supported on four bundles of cilia, called "balancers", that sense its orientation. The statocyst is protected by a transparent dome made of long, immobile cilia. A ctenophore does not automatically try to keep the statolith resting equally on all the balancers. Instead its response is determined by the animal's "mood", in other words the overall state of the nervous system. For example, if a ctenophore with trailing tentacles captures prey, it will often put some comb rows into reverse, spinning the mouth towards the prey.

Answer: aboral organ

<hl> The largest single sensory feature is the aboral organ (at the opposite end from the mouth). <hl> Its main component is a statocyst, a balance sensor consisting of a statolith, a solid particle supported on four bundles of cilia, called "balancers", that sense its orientation. The statocyst is protected by a transparent dome made of long, immobile cilia. A ctenophore does not automatically try to keep the statolith resting equally on all the balancers. Instead its response is determined by the animal's "mood", in other words the overall state of the nervous system. For example, if a ctenophore with trailing tentacles captures prey, it will often put some comb rows into reverse, spinning the mouth towards the prey.

The largest single sensory feature is the <hl> aboral organ <hl> (at the opposite end from the mouth). Its main component is a statocyst, a balance sensor consisting of a statolith, a solid particle supported on four bundles of cilia, called "balancers", that sense its orientation. The statocyst is protected by a transparent dome made of long, immobile cilia. A ctenophore does not automatically try to keep the statolith resting equally on all the balancers. Instead its response is determined by the animal's "mood", in other words the overall state of the nervous system. For example, if a ctenophore with trailing tentacles captures prey, it will often put some comb rows into reverse, spinning the mouth towards the prey.


Question: Where is the aboral organ located?

Answer: at the opposite end from the mouth

<hl> The largest single sensory feature is the aboral organ ( at the opposite end from the mouth ). <hl> Its main component is a statocyst, a balance sensor consisting of a statolith, a solid particle supported on four bundles of cilia, called "balancers", that sense its orientation. The statocyst is protected by a transparent dome made of long, immobile cilia. A ctenophore does not automatically try to keep the statolith resting equally on all the balancers. Instead its response is determined by the animal's "mood", in other words the overall state of the nervous system. For example, if a ctenophore with trailing tentacles captures prey, it will often put some comb rows into reverse, spinning the mouth towards the prey.

The largest single sensory feature is the aboral organ (<hl> at the opposite end from the mouth <hl>). Its main component is a statocyst, a balance sensor consisting of a statolith, a solid particle supported on four bundles of cilia, called "balancers", that sense its orientation. The statocyst is protected by a transparent dome made of long, immobile cilia. A ctenophore does not automatically try to keep the statolith resting equally on all the balancers. Instead its response is determined by the animal's "mood", in other words the overall state of the nervous system. For example, if a ctenophore with trailing tentacles captures prey, it will often put some comb rows into reverse, spinning the mouth towards the prey.

The largest single sensory feature is the aboral organ ( <hl> at the opposite end from the mouth <hl> ).


Question: What protects the statocyst?

Answer: a transparent dome made of long, immobile cilia

The largest single sensory feature is the aboral organ (at the opposite end from the mouth). Its main component is a statocyst, a balance sensor consisting of a statolith, a solid particle supported on four bundles of cilia, called "balancers", that sense its orientation. <hl> The statocyst is protected by a transparent dome made of long, immobile cilia . <hl> A ctenophore does not automatically try to keep the statolith resting equally on all the balancers. Instead its response is determined by the animal's "mood", in other words the overall state of the nervous system. For example, if a ctenophore with trailing tentacles captures prey, it will often put some comb rows into reverse, spinning the mouth towards the prey.

The largest single sensory feature is the aboral organ (at the opposite end from the mouth). Its main component is a statocyst, a balance sensor consisting of a statolith, a solid particle supported on four bundles of cilia, called "balancers", that sense its orientation. The statocyst is protected by <hl> a transparent dome made of long, immobile cilia <hl>. A ctenophore does not automatically try to keep the statolith resting equally on all the balancers. Instead its response is determined by the animal's "mood", in other words the overall state of the nervous system. For example, if a ctenophore with trailing tentacles captures prey, it will often put some comb rows into reverse, spinning the mouth towards the prey.

The statocyst is protected by <hl> a transparent dome made of long, immobile cilia <hl> .