Ctenophora

For the genus of crane flies, see Ctenophora (genus).

Comb jellies Temporal range: Cambrian – Recent. PreЄ Є O S D C P T J K Pg N
"Ctenophorae" from Ernst Haeckel's Kunstformen der Natur, 1904
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Subkingdom:	Eumetazoa
Phylum:	Ctenophora Eschscholtz, 1829
Classes
Tentaculata Nuda

The Ctenophora ( /tɨˈnɒfərə/; singular ctenophore, /ˈtɛnəfɔər/ or /ˈtiːnəfɔər/; from the Greek κτείς kteis 'comb' and φέρω pherō 'carry'; commonly known as comb jellies) are a phylum of animals that live in marine waters worldwide. Their most distinctive feature is the "combs", groups of cilia that they use for swimming, and they are the largest animals that swim by means of cilia – adults of various species range from a few millimeters to 1.5 meters (59 in) in size. Like cnidarians, their bodies consist of a mass of jelly with one layer of cells on the outside and another lining the internal cavity. In ctenophores these layers are two cells deep while those in cnidarians are only one cell deep. Ctenophores also resemble cnidarians in having a decentralized nerve net rather than a brain. Some authors combined ctenophores and cnidarians in one phylum, Coelenterata, as both groups rely on water flow through the body cavity for both digestion and respiration. Increasing awareness of the differences persuaded more recent authors to classify them in separate phyla.

Almost all ctenophores are predators, taking prey ranging from microscopic larvae and rotifers to the adults of small crustaceans; the exceptions are juveniles of two species, which live as parasites on the salps on which adults of their species feed. In favorable circumstances ctenophores can eat ten times their own weight in a day. There are only 100–150 validated species and possibly another 25 that have not been fully described and named. The textbook examples are cydippids with egg-shaped bodies and a pair of retractable tentacles fringed with tentilla ("little tentacles") that are covered with colloblasts, sticky cells that capture prey. The phylum has a wide range of body forms, including the flattened deep-sea platyctenids, in which the adults of most species lack combs, and the coastal beroids, which lack tentacles and prey on other ctenophores by using huge mouths armed with groups of large, stiffened cilia that act as teeth. These variations enable different species to build huge populations in the same area, because they specialize in different types of prey, which they capture by as wide a range of methods as spiders use.

Most species are hermaphrodites, in other words a single animal can produce both eggs and sperm; if they are both produced at the same time, the animal is a simultaneous hermaphrodite, and if the eggs and sperm mature at different times, the animal is a sequential hermaphrodite. Fertilization is generally external, although platyctenids' eggs are fertilized inside their parents' bodies and kept there until they hatch. The young are generally planktonic and in most species look like miniature cydippids, gradually changing into the adult shape as they grow. The exceptions are the beroids, whose young are miniature beroids with large mouths and no tentacles, and the platyctenids, whose young live as cydippid-like plankton until they reach near-adult size, but then sink to the bottom and rapidly metamorphose into the adult form. In at least some species, juveniles are capable of reproduction before reaching the adult size and shape. The combination of hermaphroditism and early reproduction enables small populations to grow at an explosive rate.

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

Despite their soft, gelatinous bodies, fossils thought to represent ctenophores, apparently with no tentacles but many more comb-rows than modern forms, have been found in lagerstätten as far back as the early Cambrian, about 525 million years ago. The position of the ctenophores in the evolutionary family tree of animals has long been debated, and the majority view at present, based on molecular phylogenetics, is that cnidarians and bilaterians are more closely related to each other than either is to ctenophores. A recent molecular phylogenetics analysis concluded that the common ancestor of all modern ctenophores was cydippid-like, and that all the modern groups appeared relatively recently, probably after the Cretaceous-Tertiary extinction 65.5 million years ago. Evidence accumulating since the 1980s indicates that the "cydippids" are not monophyletic, in other words do not include all and only the descendants of a single common ancestor, because all the other traditional ctenophore groups are descendants of various cydippids.

Distinguishing features

Further information: Sponge, Cnidaria, and Bilateria

Ctenophores form an animal phylum that is more complex than sponges, about as complex as cnidarians (jellyfish, sea anemones, etc.), and less complex than bilaterians, which include almost all other animals. Unlike sponges, both ctenophores and cnidarians have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Ctenophores are distinguished from all other animals by having colloblasts that capture prey by squirting glue on them, although a few ctenophore species lack them.^[1][2]

Like sponges and cnidarians, ctenophores have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians and ctenophores; more complex animals have three main cell layers and no intermediate jelly-like layer. Hence ctenophores and cnidarians have traditionally been labelled diploblastic, along with sponges.^[1][3] Both ctenophores and cnidarians have a type of muscle that, in more complex animals, arises from the middle cell layer,^[4] and as a result some recent text books classify ctenophores as triploblastic,^[5] while others still regard them as diploblastic.^[1]

Ranging from about 1 millimeter (0.039 in) to 1.5 meters (4.9 ft) in size,^[5][6] ctenophores are the largest non-colonial animals that use cilia ("hairs") as their main method of locomotion.^[5] Most species have eight strips, called comb rows, that run the length of their bodies and bear comb-like bands of cilia, called "ctenes," stacked along the comb rows so that when the cilia beat, those of each comb touch the comb below.^[5] The name "ctenophora" means "comb-bearing", from the Greek κτείς (stem-form κτεν-) meaning "comb" and the Greek suffix -φορος meaning "carrying".^[7]

Comparison with other major animal groups

	Sponges[8][9]	Cnidarians[1][3]	Ctenophores[1][5]	Bilateria[1]
Cnidocytes	No	Yes	No
Colloblasts	No		In most species[2]	No
Digestive and circulatory organs	No			Yes
Number of main cell layers	Two, with jelly-like layer between them		Debate about whether two[1] or three[4][5]	Three
Cells in each layer bound together	No, except that Homoscleromorpha have basement membranes.[10]	Yes: Inter-cell connections; basement membranes
Sensory organs	No	Yes
Number of cells in middle "jelly" layer	Many	Few		(Not applicable)
Cells in outer layers can move inwards and change functions	Yes	No		(Not applicable)
Nervous system	No	Yes, simple		Simple to complex
Muscles	None	Mostly epitheliomuscular	Mostly myoepithelial	Mostly myocytes

Description

For a phylum with relatively few species, ctenophores have a wide range of body plans.^[5] Coastal species need to be tough enough to withstand waves and swirling sediment particles, while some oceanic species are so fragile that it is very difficult to capture them intact for study.^[2] In addition oceanic species do not preserve well,^[2] and are known mainly from photographs and from observers' notes.^[11] Hence most attention has until recently concentrated on three coastal genera – Pleurobrachia, Beroe and Mnemiopsis.^[2][12] At least two textbooks base their descriptions of ctenophores on the cydippid Pleurobrachia.^[1][5]

Since the body of many species is almost radially symmetrical, the main axis is oral to aboral (from the mouth to the opposite end). However since only two of the canals near the statocyst terminate in anal pores, ctenophores have no mirror-symmetery, although many have rotational symmetry, in other words if the animal rotates in a half-circle it looks the same as when it started.^[13]

Common features

Body layers

mouth

stomach

statocyst

anal pore

    pharynx

    tentacle sheath

    tentacle

/// "combs" (groups of cilia)

    mesoglea

Section through a Pleurobrachia-like cydippid ctenophore. Left side shows canal from stomach to tentacle, right shows canal from stomach to comb-row.^[5]

Like those of cnidarians, (jellyfish, sea anemones, etc.), ctenophores' bodies consist of a relatively thick, jelly-like mesoglea sandwiched between two epithelia, layers of cells bound by inter-cell connections and by a fibrous basement membrane that they secrete.^[1][5] The epithelia of ctenophores have two layers of cells rather than one, and some of the cells in the upper layer have several cilia per cell.^[5]

The outer layer of the epidermis (outer skin) consists of: sensory cells; cells that secrete mucus, which protects the body; and interstitial cells, which can transform into other types of cell. In specialized parts of the body the outer layer also contains colloblasts, found along the surface of tentacles and used in capturing prey, or cells bearing multiple large cilia, for locomotion. The inner layer of the epidermis contains a nerve net, and myoepithelial cells that act as muscles.^[5]

The internal cavity forms: a mouth that can usually be closed by muscles; a pharynx ("throat"); a wider area in the center that acts as a stomach; and a system of internal canals. These branch through the mesoglea to the most active parts of the animal: the mouth and pharynx; the roots of the tentacles, if present; all along the underside of each comb row; and four branches round the sensory complex at the far end from the mouth – two of these four branches terminate in anal pores. The inner surface of the cavity is lined with an epithelium, the gastrodermis. The mouth and pharynx have both cilia and well-developed muscles. In other parts of the canal system, the gastrodermis is different on the sides nearest to and furthest from the organ that it supplies. The nearer side is composed of tall nutritive cells that store nutrients in vacuoles (internal compartments), germ cells that produce eggs or sperm, and photocytes that produce bioluminescence. The side furthest from the organ is covered with ciliated cells that circulate water through the canals, punctuated by ciliary rosettes, pores that are surrounded by double whorls of cilia and connect to the mesoglea.^[5]

Feeding, excretion and respiration

When prey is swallowed, it is liquefied in the pharynx by enzymes and by muscular contractions of the pharynx. The resulting slurry is wafted through the canal system by the beating of the cilia, and digested by the nutritive cells. The ciliary rosettes in the canals may help to transport nutrients to muscles in the mesoglea. The anal pores may eject unwanted small particles, but most unwanted matter is regurgitated via the mouth.^[5]

Little is known about how ctenophores get rid of waste products produced by the cells. The ciliary rosettes in the gastrodermis may help to remove wastes from the mesoglea, and may also help to adjust the animal's buoyancy by pumping water into or out of the mesoglea.^[5]

Locomotion

The outer surface bears usually eight comb rows, 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,^[1] 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). 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.^[5] When trying to escape predators, one species can accelerate to six times its normal speed;^[14] some other species reverse direction as part of their escape behavior, by reversing the power stroke of the comb plate cilia.

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.^[15] 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.^[5]

Nervous system and senses

Ctenophores have no brain or central nervous system, but instead have a nerve net (rather like a cobweb) that forms a ring round the mouth and is densest near structures such as the comb rows, pharynx, tentacles (if present) and the sensory complex furthest from the mouth.^[5]

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.^[5]

Cydippids

Aulacoctena sp., a cydippid ctenophore

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,^[5] 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.^[1] Some species of cydippids have bodies that are flattened to various extents, so that they are wider in the plane of the tentacles.^[5]

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.^[5] 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.^[16] 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.^[17]

There are eight rows of combs that run from near the mouth to the opposite end, and are spaced evenly round the body.^[1] The "combs" beat in a metachronal rhythm rather like that of a Mexican wave.^[18] 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.^[19]

Lobates

Bathocyroe fosteri a common but fragile deep-sea lobate, oriented mouth down

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.^[5]

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,^[5] 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.^[20] Unlike cydippids, the movements of lobates' combs are coordinated by nerves rather than by via water disturbances created by the cilia, yet combs on the same row beat beat in the same Mexican wave style as the mechanically-coordinated comb rows of cydippids and beroids.^[19] This may have enabled lobates to grow larger than cydippids and to have shapes that are less egg-like.^[18]

An unusual species first described in 2000, Lobatolampea tetragona, has been classified as a lobate, although the lobes are "primitive" and the body is medusa-like when floating and disk-like when resting on the sea-bed.^[11]

Beroids

Beroe sp. swimming with open mouth, at left. This animal is 3–6 cm long.

The Beroida, also known as Nuda, have no feeding appendages, but their large pharynx, just inside the large mouth and filling most of the saclike body, bears "macrocilia" at the oral end. These fused bundles of several thousand large cilia are able to "bite" off pieces of prey that is too large to swallow whole – almost always other ctenophores.^[21] In front of the field of macrocilia, on the mouth "lips" in some species of Beroe, is a pair of narrow strips of adhesive epithelial cells on the stomach wall that "zip" the mouth shut when the animal is not feeding, by forming intercellular connections with the opposite adhesive strip. This tight closure streamlines the front of the animal when it is pursuing prey.^[22]

Other body forms

The Ganeshida have a pair of small oral lobes and a pair of tentacles. The body is circular rather than oval in cross-section, and the pharynx extends over the inner surfaces of the lobes.^[5]

The Thalassocalycida, only discovered in 1978 and known from only one species,^[23] are medusa-like, with bodies that are shortened in the oral-aboral direction, and short comb-rows on the surface furthest from the mouth, originating from near the aboral pole. They capture prey by movements of the bell and possibly by using two short tentacles.^[5]

The Cestida ("belt animals") are ribbon-shaped planktonic animals, with the mouth and aboral organ aligned in the middle of opposite edges of the ribbon. There is a pair of comb-rows along each aboral edge, and tentilla emerging from a groove all along the oral edge, which stream back across most of the wing-like body surface. Cestids can swim by undulating their bodies as well as by the beating of their comb-rows. There are two known species, with worldwide distribution in warm, and warm-temperate waters: Cestum veneris ("Venus' girdle") is among the largest ctenophores – up to 1.5 meters (4.9 ft) long, and can undulate slowly or quite rapidly. Velamen parallelum, which is typically less than 20 centimeters (0.66 ft) long, can move much faster in what has been described as a "darting motion".^[5][24]

Most Platyctenida have oval bodies that are flattened in the oral-aboral direction, with a pair of tentilla-bearing tentacles on the aboral surface. They cling to and creep on surfaces by everting the pharynx and using it as a muscular "foot". All but one of the known platyctenid species lack comb-rows.^[5] Platyctenids are usually cryptically-colored, live on rocks, algae, or the body surfaces of other invertebrates, and are often revealed by their long tentacles with many sidebranches, seen streaming off the back of the ctenophore into the current.

Reproduction and development

Cydippid larva of Bolinopsis sp., a few mm long.

Adults of most species can regenerate tissues that are damaged or removed,^[25] although only platyctenids reproduce by cloning, splitting off from the edges of their flat bodies fragments that develop into new individuals.^[5]

Almost all species are hermaphrodites, in other words they function as both males and females at the same time – except that in two species of the genus Ocryopsis individuals remain of the same single sex all their lives. The gonads are located in the parts of the internal canal network under the comb rows, and eggs and sperm are released via pores in the epidermis. Fertilization is external in most species, but platyctenids use internal fertilization and keep the eggs in brood chambers until they hatch. Self-fertilization has occasionally been seen in species of the genus Mnemiopsis,^[5] and it is thought that most of the hermaphroditic species are self-fertile.^[2]

Development of the fertized eggs is direct, in other words there is no distinctive larval form, and juveniles of all groups generally resemble miniature cydippid adults. In the genus Beroe the juveniles, like the adults, lack tentacles and tentacle sheaths. In most species the juveniles gradually develop the body forms of their parents. In some groups, such as the flat, bottom-dwelling platyctenids, the juveniles behave more like true larvae, as they live among the plankton and thus occupy a different ecological niche from their parents and attain the adult form by a more radical metamorphosis,^[5] after dropping to the sea-floor.^[2]

At least in some species, juvenile ctenophores appear capable of producing small quantities of eggs and sperm while they are well below adult size, and adults produce eggs and sperm for as long as they have sufficient food. If they run short of food, they first stop producing eggs and sperm, and then shrink in size. When the food supply improves, they grow back to normal size and then resume reproduction. These features make ctenophores capable of increasing their populations very quickly.^[2]

Colors and bioluminescence

Light diffracting along the comb rows of a Mertensia ovum. The right lower portion of the body is regenerating from previous damage.

Undescribed deep-sea species known as "Tortugas red", with trailing tentacles and clearly visible tentilla

Most ctenophores that live near the surface are mostly colorless and almost transparent. However some deeper-living species are strongly pigmented, for example the species known as "Tortugas red"^[26] (see illustration here), which has not yet been formally described.^[2] Platyctenids generally live attached to other sea-bottom organisms, and often have similar colors to these host organisms.^[2] The gut of the deep-sea genus Bathocyroe is red, which hides the bioluminescence of copepods it has swallowed.^[20]

The comb rows of most planktonic ctenophores produce a rainbow effect, which is not caused by bioluminescence but by the scattering of light as the combs move.^[2][27] Most species are also bioluminescent, but the light is usually blue or green and can only been seen in darkness.^[2] However some significant groups, including all known platyctenids and the cydippid genus Pleurobrachia, are incapable of bioluminescence.^[28]

When some species, including Bathyctena chuni, Euplokamis stationis and Eurhamphaea vexilligera, are disturbed, they produce secretions (ink) that luminesce at much the same wavelengths as their bodies. Juveniles will luminesce more brightly in relation to their body size than adults, whose luminescence is diffused over their bodies. Detailed statistical investigation has not suggested the function of ctenophores' bioluminescence nor produced any correlation between its exact color and any aspect of the animals' environments, such as depth or whether they live in coastal or mid-ocean waters.^[29]

Ecology

Distribution

Ctenophores are found in most marine environments: from polar waters to the tropics; near coasts and in mid-ocean; from the surface waters to the ocean depths.^[2] The best-understood are the genera Pleurobrachia, Beroe and Mnemiopsis, as these planktonic coastal forms are among the most likely to be collected near shore.^[12][20] No ctenophores have been found in fresh water.

Prey and predators

Almost all ctenophores are predators – there are no vegetarians and only one genus that is partly parasitic.^[20] If food is plentiful, they can eat 10 times their own weight per day.^[30] While Beroe preys mainly on other ctenophores, other surface-water species prey on zooplankton (planktonic animals) ranging in size from the microscopic, including mollusc and fish larvae, to small adult crustaceans such as copepods, amphipods, and even krill. Members of the genus Haeckelia prey on jellyfish and incorporate their prey's nematocysts (stinging cells) into their own tentacles instead of colloblasts.^[2] Ctenophores have been compared to spiders in their wide range of techniques from capturing prey – some hang motionless in the water using their tentacles as "webs", some are ambush predators like Salticid jumping spiders, and some dangle a sticky droplet at the end of a fine thread, as Bola spiders do. This variety explains the wide range of body forms in a phylum with rather few species.^[20] The two-tentacled "cydippid" Lampea feeds exclusively on salps, close relatives of sea-squirts that form large chain-like foating colonies, and juveniles of Lampea attach themselves like parasites to salps that are too large for them to swallow.^[20] Members of the cydippid genus Pleurobrachia and the lobate Bolinopsis often reach high population densities at the same place and time because they specialize in different types of prey: Pleurobrachia's long tentacles mainly capture relatively strong swimmers such as adult copepods, while Bolinopsis generally feeds on smaller, weaker swimmers such as rotifers and mollusc and crustacean larvae.^[31]

Ctenophores used to be regarded as "dead ends" in marine food chains because it was thought their low ratio of organic matter to salt and water made them a poor diet for other animals. It is also often difficult to identify the remains of ctenophores in the guts of possible predators, although the combs sometimes remain intact long enough to provide a clue. Detailed investigation of chum salmon, Oncorhynchus keta, showed that these fish digest ctenophores 20 times as fast as an equal weight of shrimps, and that ctenophores can provide a good diet if there are enough of them around. Beroids prey mainly on other ctenophores. Some jellyfish and turtles eat large quantities of ctenophores, and jellyfish may temporarily wipe out ctenophore populations. Since ctenophores and jellyfish often have large seasonal variations in population, most fish that prey on them are generalists, and may have a greater effect on populations than the specialist jelly-eaters. The larvae of some sea anemones are parasites on ctenophores, as are the larvae of some flatworms that parasitize fish when they reach adulthood.^[32]

Ecological impacts

Beroe ovata at the surface on the Black Sea coast

Ctenophores may balance marine ecosystems by preventing an over-abundance of copepods from eating all the phytoplankton (planktonic plants),^[33] which are the dominant marine producers of organic matter from non-organic ingredients.^[34]

On the other hand in the late 1980s the North Atlantic ctenophore Mnemiopsis leidyi was accidentally introduced into the Black Sea and Sea of Azov via the ballast tanks of ships, and has been blamed for causing sharp drops in fish catches by eating both fish larvae and small crustaceans that would otherwise feed the adult fish.^[33] Mnemiopsis is well-equipped to invade new territories, as it can breed very rapidly and tolerate a wide range of water temperatures and salinities.^[35] The impact was increased by chronic overfishing, and by eutrophication that gave the entire ecosystem a short-term boost, causing the Mnemiopsis population to increase even faster than normal^[36] – and above all by the absence of efficient predators on ctenophores.^[35] Mnemiopsis populations in those areas were eventually brought under control by the accidental introduction of the ctenophore-eating ctenophore Beroe ovata,^[2] and by a cooling of the local climate from 1991 to 1993,^[36] which significantly slowed the animal's metabolism.^[35] However the abundance of plankton in the area seems unlikely to reach pre-Mnemiopsis levels.^[37]

In the late 1990s Mnemiopsis appeared in the Caspian Sea . Beroe ovata arrived shortly after, and is expected to reduce but not eliminate the impact of Mnemiopsis. Mnemiopsis also reached the eastern Mediterranean in the late 1990s and now appears to be thriving in the North Sea and Baltic Sea.^[2]

Classification

The number of known living ctenophore species is uncertain, since many of those named and formally described have turned out to be identical to species known under other scientific names. Claudia Mills estimates that there about 100 to 150 valid species that are not duplicates, and that at least another 25, mostly deep-sea forms, have been recognized as distinct but not yet analyzed in enough detail to support a formal description and naming.^[26]

The traditional classification divides ctenophores into two classes, those with tentacles (Tentaculata) and those without (Nuda). The Nuda contains only one order (Beroida) and family (Beroidae), and two genera, Beroe (several species) and Neis (one species).^[26]

The Tentaculata are divided into the following eight orders:^[26]

• Cydippida, egg-shaped animals with long tentacles^[5]
• Lobata, with paired thick lobes^[5]
• Platyctenida, flattened animals that live on or near the sea-bed; most lack combs as adults, and use their pharynges as suckers to attach themselves to surfaces^[5]
• Ganeshida, with a pair of small lobes round the mouth, but an extended pharynx like that of platyctenids^[5]
• Cambojiida
• Cryptolobiferida
• Thalassocalycida, with short tentacles and a jellyfish-like "umbrella"^[5]
• Cestida, ribbon-shaped and the largest ctenophores^[5]

Evolutionary history

Fossil record

Further information: Ctenorhabdotus capulus,  Fasciculus vesanus,  Xanioascus canadensis,  Archaeocydippida hunsrueckiana, and  Paleoctenophora brasseli

Because of their soft, gelatinous bodies, ctenophores are extremely rare as fossils, and fossils that have been interpreted as ctenophores have been found only in lagerstätten, places where the environment was exceptionally suited to preservation of soft tissue. Until the mid-1990s only two specimens good enough for analysis were known, both from the early Devonian period. Three additional putative species were then found in the Burgess Shale and other Canadian rocks of similar age, about 505 million years ago in the mid-Cambrian period. All three apparently lacked tentacles but had between 24 and 80 comb rows, far more than the 8 typical of living species. They also appear to have had internal organ-like structures unlike anything found in living ctenophores. One of the fossil species first reported in 1996 had a large mouth, apparently surrounded by a folded edge that may have been muscular.^[38] Evidence from China a year later suggests that such ctenophores were widespread in the Cambrian, but perhaps very different from modern species – for example one fossil's comb-rows were mounted on prominent vanes.^[39]

The early Cambrian sessile frond-like fossil Stromatoveris, from China's Chengjiang lagerstätte and dated to about 525 million years ago, is very similar to Vendobionta of the preceding Ediacaran period. De-Gan Shu, Simon Conway Morris et al. found on its branches what they considered rows of cilia, used for filter feeding. They suggested that Stromatoveris was an evolutionary "aunt" of ctenophores, and that ctenophores originated from sessile animals whose descendants became swimmers and changed the cilia from a feeding mechanism to a propulsion system.^[40]

Family tree

Further information: Phylogeny

Metazoa	Glass sponges Demosponges Calcareous sponges Eumetazoa Ctenophora Planulozoa Cnidaria Anthozoa (sea anemones and corals) Medusozoa (jellyfish and hydras) Placozoa Bilateria Myxozoa Other Bilateria (more complex)

Position of Ctenophora in the family tree of animals^[41][42][43]

It is difficult to reconstruct the early stages in the evolutionary "family tree" of animals using only morphology (their shapes and structures), because the large differences between Porifera (sponges), Cnidaria (jellyfish, sea anemones, etc.), Ctenophora, Placozoa and Bilateria (all the more complex animals) make comparisons difficult. Hence reconstructions now rely largely or entirely on molecular phylogenetics, which groups organisms according to similarities and differences in their biochemistry, usually in their DNA or RNA.^[44]

It is now generally thought that the Calcarea (sponges with calcium carbonate spicules) are more closely related to Cnidaria, Ctenophora (comb jellies) and Bilateria (all the more complex animals) than they are to the other groups of sponges.^[41][45][46] In 1866 it was proposed that Cnidaria and Ctenophora were more closely related to each other than to Bilateria and formed a group called Coelenterata ("hollow guts"), because Cnidaria and Ctenophora both rely on the flow of water in and out of a single cavity for feeding, excretion and respiration. In 1881 it was proposed that Ctenophora and Bilateria were more closely related to each other, since they shared features that Cnidaria lack, for example muscles in the middle layer (mesoglea in Ctenophora, mesoderm in Bilateria). More recent analyses indicate that these similarities are rather vague, and the current view, based on molecular phylogenetics, is that Cnidaria and Bilateria are more closely related to each other than either is to Ctenophora. This grouping of Cnidaria and Bilateria has been labelled "Planulozoa" because it suggests that the earliest Bilateria were similar to the planula larvae of Cnidaria.^[42][43]

In 2005 Katja Seipel and Volker Schmid suggested that cnidarians and ctenophores are simplified descendants of triploblastic animals, since ctenophores and the medusa stage of some cnidarians have striated muscle, which in bilaterians arises from the mesoderm. They did not commit themselves on whether bilaterians evolved from early cnidarians or from the hypothesized triploblastic ancestors of cnidarians.^[4] A study in 2008 of 150 genes in 21 genera proposed a third hypothesis, that sponges and cnidarians are more closely related to each other than either is to ctenophores.^[47]

	Mertensiidae (cydippids) Platyctenida Pleurobrachiidae (cydippids) Lobata Thalassocalycida Cestida Haeckeliidae (cydippids) Beroida

Relationships within the Ctenophora.^[48]

Since all modern ctenophores except the beroids have cydippid-like larvae, it has widely been assumed that their last common ancestor also resembled cydippids, having an egg-shaped body and a pair of retractable tentacles. Richard Harbison's purely morphological analysis in 1985 concluded that the cydippids are not monophyletic, in other words do not contain all and only the descendants of a single common ancestor that was itself a cydippid. Instead he found that various cydippid families were more similar to members of other ctenophore orders than to other cydippids. He also suggested that the last common ancestor of modern ctenophores was either cydippid-like or beroid-like.^[49] A molecular phylogeny analysis in 2001, using 26 species including 4 recently-discovered ones, concluded that the cydippids are not monophyletic and that the last common ancestor of modern ctenophores was cydippid-like. It also found that the genetic differences between these species were very small – so small that the relationships between the Lobata, Cestida and Thalassocalycida remained uncertain. This suggests that the last common ancestor of modern ctenophores was relatively recent, and perhaps was lucky enough to survive the Cretaceous-Tertiary extinction 65.5 million years ago while other lineages perished. When the analysis was broadened to include representatives of other phlya, it concluded that cnidarians are probably more closely related to bilaterians than either group is to ctenophores but that this diagnosis is uncertain.^[48]

Further reading

• R. S. K. Barnes, P. Calow, P. J. W. Olive, D. W. Golding, J. I. Spicer, The invertebrates – a synthesis, 3rd ed, Blackwell, 2001, ch. 3.4.3, p. 63, ISBN 0-632-04761-5
• R. C. Brusca, G. J. Brusca, Invertebrates, 2nd Ed, Sinauer Associates, 2003, ch. 9, p. 269, ISBN 0-87893-097-3
• J. Moore, An Introduction to the Invertebrates, Cambridge Univ. Press, 2001, ch. 5.4, p. 65, ISBN 0-521-77914-6
• W. Schäfer, Ctenophora, Rippenquallen, in W. Westheide and R. Rieger: Spezielle Zoologie Band 1, Gustav Fischer Verlag, Stuttgart 1996
• Bruno Wenzel, Glastiere des Meeres. Rippenquallen (Acnidaria), 1958, ISBN 3-7403-0189-9
• Mark Shasha, Night of the Moonjellies, 1992, Simon & Schuster, ISBN 0-6717-7565-0

References

1. ^ ^{a b c d e f g h i j k l} Hinde, R.T., (1998). "The Cnidaria and Ctenophora". In Anderson, D.T.,. Invertebrate Zoology. Oxford University Press. pp. 28–57. ISBN 0195513681. 
2. ^ ^{a b c d e f g h i j k l m n o p} Mills, C.E.. "Ctenophores – some notes from an expert". http://faculty.washington.edu/cemills/Ctenophores.html. Retrieved 2009-02-05. 
3. ^ ^{a b} Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. pp. 111–124. ISBN 0030259827. 
4. ^ ^{a b c} Seipel, K., and Schmid, V. (June 2005). "Evolution of striated muscle: Jellyfish and the origin of triploblasty". Developmental Biology 282 (1): 14–26. doi:10.1016/j.ydbio.2005.03.032. PMID 15936326. 
5. ^ ^{a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak} Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. pp. 182–195. ISBN 0030259827. 
6. ^ Viitasalo, S., Lehtiniemi, M., and Katajisto, T. (2008). "The invasive ctenophore Mnemiopsis leidyi overwinters in high abundances in the subarctic Baltic Sea". Journal of Plankton Research 30 (12): 1431–1436. doi:10.1093/plankt/fbn088. 
7. ^ Trumble, W., and Brown, L. (2002). "Ctenophore". Shorter Oxford English Dictionary. Oxford University Press 
8. ^ Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. pp. 76–97. ISBN 0030259827. 
9. ^ Bergquist, P.R., (1998). "Porifera". In Anderson, D.T.,. Invertebrate Zoology. Oxford University Press. pp. 10–27. ISBN 0195513681. 
10. ^ Exposito, J-Y., Cluzel, C., Garrone, R., and Lethias, C. (2002). "Evolution of collagens". The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology 268 (3): 302–316. doi:10.1002/ar.10162. PMID 12382326. 
11. ^ ^{a b} Horita, T. (March 2000). "An undescribed lobate ctenophore, Lobatolampea tetragona gen. nov. & spec. nov., representing a new family, from Japan". Zool. Med. Leiden 73 (30): 457–464. http://www.repository.naturalis.nl/document/44309. Retrieved 2009-01-03. 
12. ^ ^{a b} Haddock, S.H.D (2004). "A golden age of gelata: past and future research on planktonic ctenophores and cnidarians". Hydrobiologia 530/531: 549–556. doi:10.1007/s10750-004-2653-9. http://www.lifesci.ucsb.edu/~haddock/abstracts/haddock_gelata.pdf. Retrieved 2009-02-03. 
13. ^ Martindale, M.Q., and Henry, J.Q. (October 1999). "Intracellular Fate Mapping in a Basal Metazoan, the Ctenophore Mnemiopsis leidyi, Reveals the Origins of Mesoderm and the Existence of Indeterminate Cell Lineages". Developmental Biology 214 (2): 243–257. doi:10.1006/dbio.1999.9427. PMID 10525332. 
14. ^ Kreps, T.A., Purcell, J.E., and Heidelberg, K.B. (1997). "Escape of the ctenophore Mnemiopsis leidyi from the scyphomedusa predator Chrysaora quinquecirrha". Marine Biology 128 (3): 441–446. doi:10.1007/s002270050110. 
15. ^ Mills, C. E. (1984). "Density is altered in hydromedusae and ctenophores in response to changes in salinity". Biological Bulletin 166 (1): 206–215. doi:10.2307/1541442. http://jstor.org/stable/1541442. 
16. ^ Mills, C.E.; R.L. Miller (February 1984). "Ingestion of a medusa (Aegina citrea) by the nematocyst-containing ctenophore (Haeckelia rubra, formerly Euchlora rubra): phylogenetic implications.". Marine Biology 78 (2): 215–221. doi:10.1007/BF00394704. 
17. ^ Mackie, G.O.; Mills, C.E. and Singla, C.L. (March 1988). "Structure and function of the prehensile tentilla of Euplokamis (Ctenophora, Cydippida)". Zoomorphology (Berlin / Heidelberg: Springer) 107 (6): 319–337. doi:10.1007/BF00312216. 
18. ^ ^{a b} Craig, C.L., and Okubo, A. (April 1990). "Physical constraints on the evolution of ctenophore size and shape". Evolutionary Ecology 4 (2): 115–129. doi:10.1007/BF02270909. 
19. ^ ^{a b} Tamm, Sidney L. (1973). "MECHANISMS OF CILIARY CO-ORDINATION IN CTENOPHORES". Journal of Experimental Biology 59: 231–245. 
20. ^ ^{a b c d e f} Haddock, S.H.D. (2007). "Comparative feeding behavior of planktonic ctenophores". Integrative and Comparative Biology 47 (6): 847–853. doi:10.1093/icb/icm088. 
21. ^ Tamm, S.L.; Tamm, S. (1985). "Visualization of changes in ciliary tip configuration caused by sliding displacement of microtubules in macrocilia of the ctenophore Beroe". Journal of Cell Science 79: 161–179. 
22. ^ Tamm, Sidney L.; Tamm, Signhild (1991). "Reversible epithelial adhesion closes the mouth of Beroe, a carnivorous marine jelly". Biological Bulletin 181: 463–473. 
23. ^ Gibbons, M. J., Richardson, A. J., Angel, M. V., Buecher, E., Esnal, G., Fernandez Alamo, M. A., Gibson, R., Itoh, H., Pugh, P., Boettger-Schnack, R. and Thuesen, E. (March 2005). "What determines the likelihood of species discovery in marine holozooplankton: is size, range or depth important?". Oikos 109: 567–576. doi:10.1111/j.0030-1299.2005.13754.x. http://academic.evergreen.edu/t/thuesene/Gibbonsetal2005.pdf. Retrieved 2009-01-03. 
24. ^ Wrobel, David; Mills, Claudia (1998 and 2003). Pacific Coast Pelagic Invertebrates: A Guide to the Common Gelatinous Animals. Sea Challengers and Monterey Bay Aquarium. pp. 108. ISBN 0930118235. 
25. ^ Martindale, M.Q. (December 1986). "The ontogeny and maintenance of adult symmetry properties in the ctenophore, Mnemiopsis mccradyi". Developmental Biology 118 (2): 556–576. doi:10.1016/0012-1606(86)90026-6. PMID 2878844. 
26. ^ ^{a b c d} Mills, C.E. (May 2007). "Phylum Ctenophora: list of all valid scientific names". http://faculty.washington.edu/cemills/Ctenolist.html. Retrieved 2009-02-10. 
27. ^ Welch, Victoria; J P Vigneron; V Lousse & A Parker (2006). "Optical properties of the iridescent organ of the comb-jellyfish Beroe cucumis (Ctenophora)" (PDF). Physical Review E 73: 41916–7. Bibcode 2006PhRvE..73d1916W. doi:10.1103/PhysRevE.73.041916. http://perso.fundp.ac.be/~jpvigner/BioPhotonics/beroe.pdf. 
28. ^ Haddock, S.H.D.; Case, J.F. (1995). "Not All Ctenophores Are Bioluminescent: Pleurobrachia". Biological Bulletin 189 (3): 356–362. doi:10.2307/1542153. JSTOR 1542153. http://www.biolbull.org/cgi/reprint/189/3/356.pdf. Retrieved 2009-02-10. 
29. ^ Haddock, S.H.D., and Case, J.F. (April 1999). "Bioluminescence spectra of shallow and deep-sea gelatinous zooplankton: ctenophores, medusae and siphonophores". Marine Biology 133: 571–582. doi:10.1007/s002270050497. http://www.lifesci.ucsb.edu/~haddock/abstracts/haddock_spectra.pdf. Retrieved 2009-02-10. 
30. ^ Reeve, M.R. and Walter, M.A. (1978). "Laboratory studies of ingestion and food utilization in lobate and tentaculate ctenophores". Limnology and Oceanography 23 (4): 740–751. doi:10.4319/lo.1978.23.4.0740. http://aslo.org/lo/toc/vol_23/issue_4/0740.pdf. Retrieved 2009-02-12. 
31. ^ Costello, John H.; Coverdale, Rebecca (1998). "Planktonic Feeding and Evolutionary Significance of the Lobate Body Plan within the Ctenophora". Biological Bulletin 195 (2): 247–248. doi:10.2307/1542863. JSTOR 1542863. http://www.biolbull.org/cgi/reprint/195/2/247.pdf. Retrieved 2009-02-12. 
32. ^ Arai, M.N. (2005). "Predation on pelagic coelenterates: a review". Journal of the Marine Biological Association of the United Kingdom 85: 523–536. doi:10.1017/S0025315405011458. http://www.seaturtle.org/PDF/Arai_2005_JMarBiolAssUK.pdf. Retrieved 2009-02-12. 
33. ^ ^{a b} Chandy,S.T., and Greene, C.H. (1995). "Estimating the predatory impact of gelatinous zooplankton". Limnology and Oceanography 40 (5): 947–955. doi:10.4319/lo.1995.40.5.0947. http://aslo.org/lo/toc/vol_40/issue_5/0947.pdf. Retrieved 2009-02-12. 
34. ^ Field, C. B., Behrenfeld, M. J., Randerson, J. T. and Falkowski, P. (July 1998). "Primary Production of the Biosphere: Integrating Terrestrial and Oceanic Components". Science 281 (5374): 237–240. Bibcode 1998Sci...281..237F. doi:10.1126/science.281.5374.237. PMID 9657713. http://www.sciencemag.org/cgi/content/full/sci;281/5374/237. Retrieved 2008-09-13. 
35. ^ ^{a b c} Purcell, J.E., Shiganova, T.A., Decker, M.B., and Houde, E.D. (2001). "The ctenophore Mnemiopsis in native and exotic habitats: U.S. estuaries versus the Black Sea basin". Hydrobiologia 451: 145–176. doi:10.1023/A:1011826618539. http://issg.org/database/species/reference_files/mnelei/Purcell%20et%20al.pdf. Retrieved 2009-02-12. 
36. ^ ^{a b} Oguz, T., Fach, B., and Salihoglu, B. (2008). "Invasion dynamics of the alien ctenophore Mnemiopsis leidyi and its impact on anchovy collapse in the Black Sea". Journal of Plankton Research 30 (12): 1385–1397. doi:10.1093/plankt/fbn094. 
37. ^ Kamburska, L. (2006). "Effects of Beroe cf ovata on gelatinous and other zooplankton along the Bulgarian Black Sea Coast". In Dumont, H., Shiganova, T.A., and Niermann, U.. Aquatic Invasions in the Black, Caspian, and Mediterranean Seas. Springer Netherlands. pp. 137–154. doi:10.1007/1-4020-2152-6_5. ISBN 978-1-4020-1866-4. 
38. ^ Conway Morris, S.; Collins, D. H. (March 1996). "Middle Cambrian Ctenophores from the Stephen Formation, British Columbia, Canada". Philosophical Transactions of the Royal Society: Biological Sciences (London: The Royal Society) 351 (1337): 279–308. doi:10.1098/rstb.1996.0024. http://www.jstor.org/pss/56388. Retrieved 2009-02-14. 
39. ^ Conway Morris, S. (2003). "The Cambrian "explosion" of metazoans and molecular biology: would Darwin be satisfied?". International Journal of Developmental Biology 47 (7-8): 505–515. PMID 14756326. http://www.ijdb.ehu.es/fullaccess/fulltext.03078/ft505.pdf. Retrieved 2009-02-14. 
40. ^ Shu, D.-G.; Conway Morris, S., Han, J., Li, Y, et al. (2006). "Lower Cambrian Vendobionts from China and Early Diploblast Evolution". Science 312 (5774): 731–734. Bibcode 2006Sci...312..731S. doi:10.1126/science.1124565. PMID 16675697. http://kasprzyk.homeip.net/~alex/notes/Vendobionts.pdf. Retrieved 2009-02-14. 
41. ^ ^{a b} Borchiellini, C., Manuel, M., Alivon, E., Boury-Esnault, N., Vacelet J., and Le Parco, Y. (2001). "Sponge paraphyly and the origin of Metazoa". Journal of Evolutionary Biology 14 (1): 171–179. doi:10.1046/j.1420-9101.2001.00244.x. 
42. ^ ^{a b} Wallberg, A., Thollesson, M., , Farris, J.S., and Jondelius, U. (2004). "The phylogenetic position of the comb jellies (Ctenophora) and the importance of taxonomic sampling". Cladistics 20: 558–578. doi:10.1111/j.1096-0031.2004.00041.x. 
43. ^ ^{a b} Collins, A.G. (2002). "Phylogeny of Medusozoa and the Evolution of Cnidarian Life Cycles" (PDF). Journal of Evolutionary Biology 15 (3): 418–432. doi:10.1046/j.1420-9101.2002.00403.x. http://cima.uprm.edu/~n_schizas/CMOB_8676/Collins2002.pdf. Retrieved 2008-11-27. 
44. ^ Halanych, K.M. (December 2004). "The New View of Animal Phylogeny" (PDF). Annual Review of Ecology, Evolution, and Systematics 35: 229–256. doi:10.1146/annurev.ecolsys.35.112202.130124. http://www.auburn.edu/academic/science_math/cosam/departments/biology/faculty/webpages/zzhalanych/Pub.pdfs/Halanych2004.pdf. Retrieved 2008-11-27. ^{[dead link]}
45. ^ Medina, M., Collins, A.G., Silberman, J.D., and Sogin, M.L. (August 2001). "Evaluating hypotheses of basal animal phylogeny using complete sequences of large and small subunit rRNA". Proceedings of the National Academy of Sciences 98 (17): 9707–9712. Bibcode 2001PNAS...98.9707M. doi:10.1073/pnas.171316998. PMC 55517. PMID 11504944. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=55517. 
46. ^ Müller, W.E.G., Li, J., Schröder, H.C., Qiao, L., and Wang, X. (2007). "The unique skeleton of siliceous sponges (Porifera; Hexactinellida and Demospongiae) that evolved first from the Urmetazoa during the Proterozoic: a review". Biogeosciences 4: 219–232. doi:10.5194/bg-4-219-2007. 
47. ^ Dunn, C.W.; Hejnol, A., David Q. Matus, D.Q., et al. (April 2008). "Broad phylogenomic sampling improves resolution of the animal tree of life". Nature 452 (7188): 745–749. Bibcode 2008Natur.452..745D. doi:10.1038/nature06614. PMID 18322464. 
48. ^ ^{a b} Podar, M.; Haddock, S.H.D, Sogin, M.L., and Harbison, G.R. (November 2001). "A Molecular Phylogenetic Framework for the Phylum Ctenophora Using 18S rRNA Genes". Molecular Phylogenetics and Evolution (Academic Press) 21 (2): 218–230. doi:10.1006/mpev.2001.1036. PMID 11697917. http://www.lifesci.ucsb.edu/~haddock/abstracts/podar_ctenophores.pdf. Retrieved 2009-02-14. 
49. ^ Harbison, G.R. (1985). "On the classification and evolution of the Ctenophora". In Conway Morris, S., George, J.D.,. Gibson, R., and Platt, H.M.. The Origins and Relationships of Lower Invertebrates. Clarendon Press. pp. 78–100. ISBN 019857181X. 

External links

• Ctenophores from the São Sebastião Channel, Brazil
• Video of ctenophores at the National Zoo in Washington DC
• Tree Of Animal Life Has Branches Rearranged, By Evolutionary Biologists
• Australian Ctenophora Fact Sheet
• The Jelly Connection – striking images, including a Beroe specimen attacking another ctenophore