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 does the 9 +3 pattern of cilia thought to do?, context: 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.


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: What direction do ctenophore swim?, context: 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.


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: Cilia can g ow up too what length?, context: 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.


Question: How do ctenophores control buoyancy?

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: How do ctenophores control buoyancy?, context: 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.


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: Ciliary rosettes pump water into what to control buoyancy?, context: 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.


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 pumping water into the mesoglea do?, context: 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.


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 does the ciliary rosettes do to decease bulk and increase density?, context: 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.


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

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: What is the largest sensory feature of the ctenophora?, context: 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.


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: Where is the aboral organ located?, context: 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.


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> .

question: What protects the statocyst?, context: 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.


Question: What is the main component of the aboral organ?

Answer: a statocyst

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. <hl> 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 (at the opposite end from the mouth). Its main component is <hl> a statocyst <hl>, 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.

Its main component is <hl> a statocyst <hl> , a balance sensor consisting of a statolith, a solid particle supported on four bundles of cilia, called "balancers", that sense its orientation.

question: What is the main component of the aboral organ?, context: 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.


Question: What is a statocyst?

Answer: a balance sensor

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. <hl> 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 (at the opposite end from the mouth). Its main component is a statocyst, <hl> a balance sensor <hl> 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: What is a statocyst?, context: 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.


Question: What is the common coastal pleurobrachia called?

Answer: sea gooseberry

<hl> Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal " sea gooseberry ," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. <hl> From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "<hl> sea gooseberry <hl>," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal " <hl> sea gooseberry <hl> ," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round.

question: What is the common coastal pleurobrachia called?, context: Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.


Question: What does the pleurobrachia have on opposite sides of its body?

Answer: a pair of long, slender tentacles

Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. <hl> From opposite sides of the body extends a pair of long, slender tentacles , each housed in a sheath into which it can be withdrawn. <hl> Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends <hl> a pair of long, slender tentacles <hl>, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

From opposite sides of the body extends <hl> a pair of long, slender tentacles <hl> , each housed in a sheath into which it can be withdrawn.

question: What does the pleurobrachia have on opposite sides of its body?, context: Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.


Question: Cydippid are typically what shape?

Answer: more or less rounded

<hl> Cydippid ctenophores have bodies that are more or less rounded , sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. <hl> From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

Cydippid ctenophores have bodies that are <hl> more or less rounded <hl>, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

Cydippid ctenophores have bodies that are <hl> more or less rounded <hl> , sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round.

question: Cydippid are typically what shape?, context: Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.


Question: The long tentacles on the pleurbrachia are protected by what?

Answer: a sheath

Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. <hl> From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. <hl> Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in <hl> a sheath <hl> into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

question: The long tentacles on the pleurbrachia are protected by what?, context: Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.


Question: Where is the mouth located on the pleuobrachia located?

Answer: at the narrow end

<hl> Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end , although some individuals are more uniformly round. <hl> From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth <hl> at the narrow end <hl>, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.

Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth <hl> at the narrow end <hl> , although some individuals are more uniformly round.

question: Where is the mouth located on the pleuobrachia located?, context: Cydippid ctenophores have bodies that are more or less rounded, sometimes nearly spherical and other times more cylindrical or egg-shaped; the common coastal "sea gooseberry," Pleurobrachia, sometimes has an egg-shaped body with the mouth at the narrow end, although some individuals are more uniformly round. From opposite sides of the body extends a pair of long, slender tentacles, each housed in a sheath into which it can be withdrawn. Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.


Question: What are the tentacles of cydipped ctenophores are usually fringed with?

Answer: tentilla

<hl> The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. <hl> The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

The tentacles of cydippid ctenophores are typically fringed with <hl> tentilla <hl> ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

question: What are the tentacles of cydipped ctenophores are usually fringed with?, context: The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.


Question: What are colloblasts?

Answer: specialized mushroom-shaped cells in the outer layer of the epidermis

The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. <hl> Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis , and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. <hl> The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are <hl> specialized mushroom-shaped cells in the outer layer of the epidermis <hl>, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

Colloblasts are <hl> specialized mushroom-shaped cells in the outer layer of the epidermis <hl> , and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk.

question: What are colloblasts?, context: The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.


Question: What makes the tentilla of euplokamis different from other cysippids?

Answer: they contain striated muscle,

The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. <hl> The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. <hl> Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: <hl> they contain striated muscle, <hl> a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

question: What makes the tentilla of euplokamis different from other cysippids?, context: The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.


Question: How many types of movements do euplokamis tentilla have?

Answer: three types of movement

The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. <hl> Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. <hl> The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have <hl> three types of movement <hl> that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

question: How many types of movements do euplokamis tentilla have?, context: The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.


Question: What does the euplokamis use the three types of movement for?

Answer: capturing prey

The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. <hl> Euplokamis' tentilla have three types of movement that are used in capturing prey : they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. <hl> The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in <hl> capturing prey <hl>: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.

Euplokamis' tentilla have three types of movement that are used in <hl> capturing prey <hl> : they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey.

question: What does the euplokamis use the three types of movement for?, context: The tentacles of cydippid ctenophores are typically fringed with tentilla ("little tentacles"), although a few genera have simple tentacles without these sidebranches. The tentacles and tentilla are densely covered with microscopic colloblasts that capture prey by sticking to it. Colloblasts are specialized mushroom-shaped cells in the outer layer of the epidermis, and have three main components: a domed head with vesicles (chambers) that contain adhesive; a stalk that anchors the cell in the lower layer of the epidermis or in the mesoglea; and a spiral thread that coils round the stalk and is attached to the head and to the root of the stalk. The function of the spiral thread is uncertain, but it may absorb stress when prey tries to escape, and thus prevent the collobast from being torn apart. In addition to colloblasts, members of the genus Haeckelia, which feed mainly on jellyfish, incorporate their victims' stinging nematocytes into their own tentacles – some cnidaria-eating nudibranchs similarly incorporate nematocytes into their bodies for defense. The tentilla of Euplokamis differ significantly from those of other cydippids: they contain striated muscle, a cell type otherwise unknown in the phylum Ctenophora; and they are coiled when relaxed, while the tentilla of all other known ctenophores elongate when relaxed. Euplokamis' tentilla have three types of movement that are used in capturing prey: they may flick out very quickly (in 40 to 60 milliseconds); they can wriggle, which may lure prey by behaving like small planktonic worms; and they coil round prey. The unique flicking is an uncoiling movement powered by contraction of the striated muscle. The wriggling motion is produced by smooth muscles, but of a highly specialized type. Coiling around prey is accomplished largely by the return of the tentilla to their inactive state, but the coils may be tightened by smooth muscle.


Question: How many rows of combs are there?

Answer: eight rows

<hl> There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body. <hl> The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.

There are <hl> eight rows <hl> of combs that run from near the mouth to the opposite end, and are spaced evenly round the body. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.

question: How many rows of combs are there?, context: There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.


Question: Where are the rows of combs located?

Answer: from near the mouth to the opposite end

<hl> There are eight rows of combs that run from near the mouth to the opposite end , and are spaced evenly round the body. <hl> The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.

There are eight rows of combs that run <hl> from near the mouth to the opposite end <hl>, and are spaced evenly round the body. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.

There are eight rows of combs that run <hl> from near the mouth to the opposite end <hl> , and are spaced evenly round the body.

question: Where are the rows of combs located?, context: There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.


Question: How are the combs spaced?

Answer: evenly round the body

<hl> There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body . <hl> The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.

There are eight rows of combs that run from near the mouth to the opposite end, and are spaced <hl> evenly round the body <hl>. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.

There are eight rows of combs that run from near the mouth to the opposite end, and are spaced <hl> evenly round the body <hl> .

question: How are the combs spaced?, context: There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.


Question: What runs from the balancer in the statocyst to the comb rows?

Answer: ciliary groove

There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. <hl> From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. <hl> This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.

There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a <hl> ciliary groove <hl> runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.

question: What runs from the balancer in the statocyst to the comb rows?, context: There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body. The "combs" beat in a metachronal rhythm rather like that of a Mexican wave. From each balancer in the statocyst a ciliary groove runs out under the dome and then splits to connect with two adjacent comb rows, and in some species runs all the way along the comb rows. This forms a mechanical system for transmitting the beat rhythm from the combs to the balancers, via water disturbances created by the cilia.


Question: What does the lobata have pair of?

Answer: lobes

<hl> The Lobata have a pair of lobes , which are muscular, cuplike extensions of the body that project beyond the mouth. <hl> Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.

The Lobata have a pair of <hl> lobes <hl>, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.

The Lobata have a pair of <hl> lobes <hl> , which are muscular, cuplike extensions of the body that project beyond the mouth.

question: What does the lobata have pair of?, context: The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.


Question: What are auricles?

Answer: gelatinous projections edged with cilia that produce water currents

The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). <hl> Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. <hl> This combination of structures enables lobates to feed continuously on suspended planktonic prey.

The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, <hl> gelatinous projections edged with cilia that produce water currents <hl> that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.

question: What are auricles?, context: The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.


Question: How many auricles do most species have?

Answer: four

The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). <hl> Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. <hl> This combination of structures enables lobates to feed continuously on suspended planktonic prey.

The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have <hl> four <hl> auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.

question: How many auricles do most species have?, context: The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.


Question: What do the auricles do?

Answer: help direct microscopic prey toward the mouth

The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). <hl> Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth . <hl> This combination of structures enables lobates to feed continuously on suspended planktonic prey.

The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that <hl> help direct microscopic prey toward the mouth <hl>. This combination of structures enables lobates to feed continuously on suspended planktonic prey.

Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that <hl> help direct microscopic prey toward the mouth <hl> .

question: What do the auricles do?, context: The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.


Question: What do lobates feed on?

Answer: suspended planktonic prey

The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. <hl> This combination of structures enables lobates to feed continuously on suspended planktonic prey . <hl>

The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on <hl> suspended planktonic prey <hl>.

This combination of structures enables lobates to feed continuously on <hl> suspended planktonic prey <hl> .

question: What do lobates feed on?, context: The Lobata have a pair of lobes, which are muscular, cuplike extensions of the body that project beyond the mouth. Their inconspicuous tentacles originate from the corners of the mouth, running in convoluted grooves and spreading out over the inner surface of the lobes (rather than trailing far behind, as in the Cydippida). Between the lobes on either side of the mouth, many species of lobates have four auricles, gelatinous projections edged with cilia that produce water currents that help direct microscopic prey toward the mouth. This combination of structures enables lobates to feed continuously on suspended planktonic prey.


Question: What does the bathocyroe and ocyropsis do to escape danger?

Answer: by clapping their lobes

Lobates have eight comb-rows, originating at the aboral pole and usually not extending beyond the body to the lobes; in species with (four) auricles, the cilia edging the auricles are extensions of cilia in four of the comb rows. Most lobates are quite passive when moving through the water, using the cilia on their comb rows for propulsion, although Leucothea has long and active auricles whose movements also contribute to propulsion. <hl> Members of the lobate genera Bathocyroe and Ocyropsis can escape from danger by clapping their lobes , so that the jet of expelled water drives them backwards very quickly. <hl> Unlike cydippids, the movements of lobates' combs are coordinated by nerves rather than by water disturbances created by the cilia, yet combs on the same row beat in the same Mexican wave style as the mechanically coordinated comb rows of cydippids and beroids. This may have enabled lobates to grow larger than cydippids and to have shapes that are less egg-like.

Lobates have eight comb-rows, originating at the aboral pole and usually not extending beyond the body to the lobes; in species with (four) auricles, the cilia edging the auricles are extensions of cilia in four of the comb rows. Most lobates are quite passive when moving through the water, using the cilia on their comb rows for propulsion, although Leucothea has long and active auricles whose movements also contribute to propulsion. Members of the lobate genera Bathocyroe and Ocyropsis can escape from danger <hl> by clapping their lobes <hl>, so that the jet of expelled water drives them backwards very quickly. Unlike cydippids, the movements of lobates' combs are coordinated by nerves rather than by water disturbances created by the cilia, yet combs on the same row beat in the same Mexican wave style as the mechanically coordinated comb rows of cydippids and beroids. This may have enabled lobates to grow larger than cydippids and to have shapes that are less egg-like.

Members of the lobate genera Bathocyroe and Ocyropsis can escape from danger <hl> by clapping their lobes <hl> , so that the jet of expelled water drives them backwards very quickly.

question: What does the bathocyroe and ocyropsis do to escape danger?, context: Lobates have eight comb-rows, originating at the aboral pole and usually not extending beyond the body to the lobes; in species with (four) auricles, the cilia edging the auricles are extensions of cilia in four of the comb rows. Most lobates are quite passive when moving through the water, using the cilia on their comb rows for propulsion, although Leucothea has long and active auricles whose movements also contribute to propulsion. Members of the lobate genera Bathocyroe and Ocyropsis can escape from danger by clapping their lobes, so that the jet of expelled water drives them backwards very quickly. Unlike cydippids, the movements of lobates' combs are coordinated by nerves rather than by water disturbances created by the cilia, yet combs on the same row beat in the same Mexican wave style as the mechanically coordinated comb rows of cydippids and beroids. This may have enabled lobates to grow larger than cydippids and to have shapes that are less egg-like.


Question: What happens when bathocyroe and ocyropsis clap their lobes together?

Answer: jet of expelled water drives them backwards very quickly.

Lobates have eight comb-rows, originating at the aboral pole and usually not extending beyond the body to the lobes; in species with (four) auricles, the cilia edging the auricles are extensions of cilia in four of the comb rows. Most lobates are quite passive when moving through the water, using the cilia on their comb rows for propulsion, although Leucothea has long and active auricles whose movements also contribute to propulsion. <hl> Members of the lobate genera Bathocyroe and Ocyropsis can escape from danger by clapping their lobes, so that the jet of expelled water drives them backwards very quickly. Unlike cydippids, the movements of lobates' combs are coordinated by nerves rather than by water disturbances created by the cilia, yet combs on the same row beat in the same Mexican wave style as the mechanically coordinated comb rows of cydippids and beroids. <hl> This may have enabled lobates to grow larger than cydippids and to have shapes that are less egg-like.

Lobates have eight comb-rows, originating at the aboral pole and usually not extending beyond the body to the lobes; in species with (four) auricles, the cilia edging the auricles are extensions of cilia in four of the comb rows. Most lobates are quite passive when moving through the water, using the cilia on their comb rows for propulsion, although Leucothea has long and active auricles whose movements also contribute to propulsion. Members of the lobate genera Bathocyroe and Ocyropsis can escape from danger by clapping their lobes, so that the <hl> jet of expelled water drives them backwards very quickly. <hl> Unlike cydippids, the movements of lobates' combs are coordinated by nerves rather than by water disturbances created by the cilia, yet combs on the same row beat in the same Mexican wave style as the mechanically coordinated comb rows of cydippids and beroids. This may have enabled lobates to grow larger than cydippids and to have shapes that are less egg-like.

question: What happens when bathocyroe and ocyropsis clap their lobes together?, context: Lobates have eight comb-rows, originating at the aboral pole and usually not extending beyond the body to the lobes; in species with (four) auricles, the cilia edging the auricles are extensions of cilia in four of the comb rows. Most lobates are quite passive when moving through the water, using the cilia on their comb rows for propulsion, although Leucothea has long and active auricles whose movements also contribute to propulsion. Members of the lobate genera Bathocyroe and Ocyropsis can escape from danger by clapping their lobes, so that the jet of expelled water drives them backwards very quickly. Unlike cydippids, the movements of lobates' combs are coordinated by nerves rather than by water disturbances created by the cilia, yet combs on the same row beat in the same Mexican wave style as the mechanically coordinated comb rows of cydippids and beroids. This may have enabled lobates to grow larger than cydippids and to have shapes that are less egg-like.