Ctenophore
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 "Ctenophorae" from Ernst Haeckel's Kunstformen der Natur, 1904
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The ctenophore (pl. ctenophores or ctenophora), also known as the comb jelly, is a phylum classically grouped with Cnidaria in the Coelenterata infrakingdom. The phylum includes the sea gooseberry (Pleurobrachia pileus) and the Venus' girdle (Cestum veneris). The word ctenophore (pronounced without the c, /tiːn.ou.fɔː(r)/) comes from Greek, kteno-, kteis, "comb" and -phore, meaning "bearer". It comes via the New Latin ctenophorus in the 19th century.
Despite their appearance, they are zoologically not true jellyfish, not least because they lack the characteristic cnidocytes. There are more than 100 varieties of ctenophore spread throughout the worlds' oceans, which form a considerable proportion of the entire plankton biomass. A few species, such as the sea gooseberry, native to the North Sea, have reached such high populations that they clog fishermen's nets, while of other species only a few examples are known. The fragile makeup of ctenophora makes research into their way of life extremely difficult; for this reason data on their lifespan is not available, but it is known that Ctenophora begin to reproduce even before they reach adulthood, and so can be assumed to have a short generation cycle.
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[edit] Body
Ctenophora are generally colourless, except for the colouration caused by algae cells with which they live in symbiosis, and are often only a few centimetres long. The exceptions are the species of the genus Cestum, which can reach an average of one and a half metres.
The species which live in deep waters can however be brightly-coloured, such as the red tortuga, which currently does not have a scientific name. The red tortuga is dark red in colour and, like many other Ctenophora, can give off light by means of bioluminescence. The colouration may serve as camouflage for the species that live on the sea bed. One species, Eurhamphaea vexilligera, can give off a luminous red tint, which may dissuade predators.
Ctenophora are almost without exception radially symmetric, their main bodily axis running between the mouth and their sensory organ, the statocyst, which lies exactly opposite from the mouth. This symmetry is superficially broken in the lower part of the creatures by the two tentacles, in the higher part by the digestive chamber, which is separated into several channels. The lower symmetry is shifted round from the higher by ninety degrees, forming a disymmetry or a biradial form.
The body consists of two transparent cell layers, which make up its outer skin (ectoderm) and inner skin (gastroderm). The ectoderm, made up of two cell layers, is mostly covered by a protective layer of slime, excreted by special glands. The gastroderm surrounds a cavity which serves as a stomach and is only accessible by the mouth opening, connected by a long, narrow gullet. Captured quarry is pre-digested in the gullet by strong enzymes and fully decomposed in the stomach. There is no separate exit from the stomach apart from two 'anal pores', which despite their name are not used for excretion, so indigestable waste must be expelled via the mouth.
The space between the inner and outer skin is taken up by the mesoglea, a thick, transparent, jelly-like layer made from collagen and connective tissue, pervaded by numerous small channels, which are used for transport and storage of nutrients. The position of the channels varies from species to species, but they mostly run directly underneath the tissues that they serve. The extracellular net of structural protein is kept upright by special cells similar to amoebas.
The mesogloea may also play a role in the lift of the creatures. Flagella found in the channels of the digestive system may serve to pump water in or out of the mesogloea, when osmotic water pressure changes, perhaps because the creature has swum out of saline sea water into coastal brackwater. Ctenophora do not possess a specific circulatory system, neither do they have any organs for breathing; gas exchange and the excretion of waste products of cell metabolism such as ammonia occur over the body's entire surface through simple diffusion. The body is pervaded by a simple net of neurons without a 'brain', which is concentrated around the gullet, tentacles, 'combs' and statocysts and is connected with the muscular cells found in the mesogloea and the inner cellular layer of the ectoderm.
[edit] Statocyst and tentacles
The statocyst is a specialised system of the ctenophore, which serves as a balancing organ and also controls its movement. It can be found on the side of the body turned away from the mouth opening and is formed by a collection of a few hundred lime cells on one side and four horizontal groups of serpentine flagella, known as the statolith. As outside influences cause the ctenophore to change its position, the statolith puts more pressure on one of the four flagella groups than on the other three. This sensation is transmitted to the ectoderm, which is pervaded by eight long "comb rows" (ctenes). The ctenes are formed from rows of cilia, which coalesce with one another in their hundreds and form flagella about two millimetres long. By erecting these discs in sequence the ctenophore can use them as an oar, which, when the eight ctenes are properly synchronised, allow it to regain its former position. A flagellum group of statocysts is needed for every quadrant and controls two ctenes as a pace maker. The rhythm is carried automatically and not by nerve impulses.
Whether heightened pressure on the flagella groups raises or lowers the stroke frequency depends on the "disposition" or geotaxis of the ctenophore; if positive, the frequency of increases in pressure is reduced, so that the ctenophore aligns itself with its mouth pointing downwards and swims away from the water's surface. If negative, the frequency increases, the ctenophore points its front end upwards and swims towards the surface. The "disposition" of the ctenophore is determined by sensations handled by the neuron net.
Most species have two opposing retractable tentacles before the mouth opening, which spring from each sheath to catch prey. On the side they often bear a row of fibrous filaments, which unlike Cnidaria do not contain stinging cells, but colloblasts or "lasso cells". These cells burst open when prey comes in contact with the tentacle. Sticky threads released from each of the colloblasts will then capture the food. The colloblasts, like the tentacle, are regularly fully regenerated.
Not all varieties have tentacles. Some instead use their muscular mouth lobes to catch food, which are simply drawn over their prey.
Ctenophora are capable of extraordinary regeneration; even if half of the creature is destroyed, often the remaining half can rebuild itself. The same is true of single organs such as the statoliths, which can be regenerated even after being completely lost.
[edit] Movement
Many Ctenophora simply let themselves drift with the current. They can however also swim short distances by means of the strokes of their flagella and by using their mouth opening as a rudder. They are the largest animal to use their flagella for movement and can reach speeds of about five centimetres a second. A possible evolutionary advantage is that constant strokes do not cause vibrations that would alert prey or predators.
Some varieties also use the muscular cells of their mouth lobes to swim, while others move by undulating their body or creeping like flatworms.
[edit] Prey and predators
Ctenophora are predators which use their tentacles to catch plankton, larvae, worms, crustaceans, Cnidaria, other Ctenophora, and sometimes small fish. When their tentacles are loaded with food, they can be retracted and wiped off. The food is then carried into the stomach either by mucus or inner cilia. The species of the genus Haeckelia feed almost exclusively on cnidaria, but do not digest their cnidocytes; instead they build them into their own tentacles as 'kleptocnides'. This 'theft' baffled zoologists for a long time as they falsely assumed ctenophora were also capable of forming cnidocytes.
Like many cnidaria, ctenophora sometimes live with various algae, which supply them with energy-rich carbohydrates through photosynthesis in a symbiotic relationship. Parasitism has only been observed in a single species, Lampea pancerina, which lives in tunicates.
Among the species who prey on ctenophora are cnidaria, sea turtles, various fish such as mackerels and lumpfish, seabirds and other ctenophora.
[edit] Habitat
All Ctenophora live in the sea, where they live in depths of up to three kilometres. Their habitat is fixed primarily by the ocean currents, in particular the tide. A few species even appear in the North Sea, such as the sea gooseberry (Pleurobrachia pileus) or Beroe gracilis.
The most well-known species live as plankton in the ocean layers near the surface. However, as they are largely transparent, extremely fragile and rarely grow longer than a few millimetres, they are unknown to most people. On the coast the nodula Pleurobrachia species are found most frequently, of which the sea gooseberries are part. Bolinopsis, Mnemiopsis and the tentacle-less Beroe can also be found fairly frequently.
About 35 species live on the sea bed. These species are ordered in the taxon of platyctenidae, due to their flattened forms which more closely resemble slugs or flatworms than jellyfish.
The ctenophora known as Mertensia ovum make up the most predominant group of plankton in the arctic waters.
[edit] Reproduction
Ctenophora reproduce sexually, with the exception of species of the order Platyctenida, which reproduce asexually. Almost all ctenophora are hermaphroditic, possessing both male and female reproductive organs, which lie directly under the 'combs' near the small channels of the mesogloea. With almost all species, when triggered by outside lighting conditions the gametes are discharged into the surrounding water through small openings in the ectoderm, the gonopores, where fertilisation also takes place. Self-fertilisation is somewhat rare and apparently appears only in the genus of Mnemiopsis. A single species, Tjalfiella tristoma, is viviparous; that is, the young grow in a womb.
After the fertilised eggs have divided twice, the ctenophore's later body symmetry has already been set; they develop over a free-floating cydippea state, which looks very similar between all ctenophora and sometimes is labelled as a larva, although usually in reality already represents a miniature version of what the creature will grow up to be. Among some extremely specialised groups such as platyctenides the cydippea and adult forms do however take separate ecological niches, so that the 'larva' label is more appropriate.
[edit] Ctenophore as an invasive species
Although ctenophores are generally hardly noticeable and their influence on an ecosystem is ostensibly very low, they can still do significant damage when they find themselves in non-native waters. The North Atlantic species Mnemiopsis leidyi was brought by ships' ballast water into the Black Sea and spread rapidly. Within ten years the anchovy fishing industry around the sea had collapsed, as the newly introduced species fed on the same plankton as the anchovy larvae. The biomass of ctenophora in the Black Sea reached a million tons at its highest point of its development.
Through the similarly sudden appearance in 1997 of another ctenophore, Beroe ovata, which feeds on Mnemiopsis leidyi, the balance swung the other way. However since then the Black Sea has been occupied by both foreign species. The same scenario with the same species has now begun to be played out in the Caspian Sea. Similarly drastic changes to the ecosystem are expected.
[edit] Early classification
Sailors have observed ctenophores since ancient times. However, the first recorded sighting only came in 1671, made by a ship's doctor. The Swedish taxonomist Carl von Linné classified them with other 'primitive' invertebrates such as sea sponges (Porifera) or cnidaria as 'zoophytes' ("animal plants"), alluding to the passive, "plant-like" character of the creatures. The French zoologist Georges Cuvier supported this classification. Only in the 19th century were ctenophora recognised as a standalone taxon.
[edit] Historical phylum
The initial classification of ctenophora has been disputed. According to cladistics, currently the leading ordering method, ctenophora are more closely related to the reflectively symmetrical bilateria than cnidaria. The fact that they have two opposing tentacles, breaking their radial symmetry and making them reflectively symmetrical, supports this. They differ from cnidaria in their possession of true muscle tissue and their 'combs'. Another important sign of ctenophore's relationship with bilateria is the form of their spermatozoa. These consist in both groups of a single, large acrosome and a subacrosomic perforation disc. Cnidarian spermatozoa, in contrast, possess several acrosomic vesicles.
For this reason the 'classical' grouping of Coelenterata stands opposite the alternative taxon of acrosomata:
Alternative 1: Coelenterata
- Eumetazoa
- Bilateria
- Coelenterata
- Cnidaria
- Ctenophora
Alternative 2: Acrosomata
- Eumetazoa
- Cnidaria
- Acrosomata
- Bilateria
- Ctenophora
In addition it has been suggested that ctenophora have a close relationship with flatworms, due to the similarities between flatworms and the flattened ctenophora of the order Platyctenida are one of the justifications for this. Most zoologists consider this resemblance superficial, and not indicative of a close relationship.
The soft bodies of ctenophores, which have no hard parts whatsoever, makes fossilisation generally very improbable, meaning that the phylogeny of ctenophora fossils is very sparsely documented. The sole fossil records, of Archaeocydippida hunsrueckiana and Paleoctenophora brasseli, date from the Devonian Period; enough details remained in the fine-grained schist of Hunsrück to make identification possible. It is disputed whether the species Maotianoascus octonarius, known from the Chengjiang Fauna of the lower Cambrian Period, is a member of the ctenophore phylum, while three species, Ctenorhabdotus capulus, Fasciculus vesanus and Xanioascus canadensis, are known from the Cambrian Burgess Shale.
[edit] Classification
Currently about a hundred species are known, which are traditionally split into the classes of Tentaculata (also known as Tentaculifera) and Nuda (also known as Atentaculata).
- The Tentaculata make up by far the largest number of species; as their name implies, they possess tentacles, although these are sometimes vestigial. They are divided into the following six orders:
- The Nuda class contains only a single order, Beroida, to which the melon jelly (Beroe gracilis) belongs. As again the name of the taxon implies, they are distinguished by the complete absence of tentacles.
Due to the continued uncertainty over the ordering of ctenophora it is currently unclear whether the above divisions correctly reflect the actual phylogeny of the taxon. They are only an accurate representation if the tentacled species developed from tentacleless ancestors. If, instead, the tentacles of the Nuda class dwindled away, it is very probable that the Tentaculata class forms a paraphyletic group, i.e. it does not include all the descendants of their common ancestor. According to the beliefs of modern systematics, cladistics, it would then be an unnatural grouping of species that were not closely related. Molecular genetic studies support the latter view and in addition regard the order Cydippida as polyphyletic; if the results of these studies are proven true, these do not include the latest common ancestor of the group and are therefore an artificial taxon.
The following diagram shows the putative phylogeny of ctenophora on the basis of morphologic and molecular genetic data (RNA):
Ctenophora |--Cydippida (Mertensiidae family) |--N. N. |--Platyctenida |--N. N. |--Cydippida (Pleurobrachidae family) |--N. N. | |--Nuda beziehungsweise Beroida | |--Cydippida (Haeckeliidae family) | |--N. N. |--Lobata |--Cestida |--Thalassocalycida Position of Ganeshida unknown
The above details are however still in doubt. For the time being the phylogeny of ctenophora must be regarded as unsettled.
[edit] References
- Much of this article is based on a translation of the corresponding German-language Wikipedia article, retrieved on 5th April 2006.
- D. T. Anderson, Invertebrate Zoology, 2nd ed, Oxford Univ. Press, 2001, Ch. 3, p. 54, ISBN 0-19-551368-1
- 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
- E. E. Ruppert, R. S. Fox, R. P. Barnes, Invertebrate Zoology – A functional evolutionary approach, Brooks/Cole 2004, ch. 8, p. 181, ISBN 0-03-025982-7
- 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
[edit] Scientific literature
- G. D. Stanley, W. Stürmer, The first fossil ctenophore from the lower devonian of West Germany, Nature 303, 1983, p. 518
- M. Q. Martindale, J. Q. Henry, Ctenophora, in S. F. Gilbert, A. M. Raunio, Embryology: Constructing the Organism, Sinauer, 1997, p. 87
- M. Podar, S. H. D. Haddock, M. L. Sogin, G. R. Harbison, A molecular phylogenetic framework for the phylum Ctenophora using 18S rRNA genes, Molecular Phylogenetics and Evolution, 21, 2001, p. 218
- T. A. Shiganova, Invasion of the Black Sea by the ctenophore Mnemiopsis leidyi and recent changes in pelagic community structure, Fisheries Oceanography, 1998, p. 305
[edit] External links
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- Washington State University - Ctenophores
