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Tunicates
Fossil range: Early Cambrian - Recent
Sea Tulips, Pyura spinifera
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Subphylum: Urochordata
Giribet et al., 2000
Classes

Ascidiacea (2,300 species)
Thaliacea
Appendicularia
Sorberacea

Tunicates, also known as urochordates, are members of the subphylum Tunicata or Urochordata, a group of underwater saclike filter feeders with incurrent and excurrent siphons that is classified within the phylum Chordata. While most tunicates live on the ocean floor and are commonly known as sea squirts and sea pork,[1] others – such as salps, doliolids and pyrosomes – live above in the pelagic zone as adults.

Most tunicates feed by filtering sea water through pharyngeal slits, but some are sub-marine predators such as the Megalodicopia hians. Like other chordates, tunicates have a notochord during their early development, but lack myomeric segmentation throughout the body and tail as adults. Tunicates lack the kidney-like metanephridial organs, and the original coelom body-cavity develops into a pericardial cavity and gonads. Except for the pharynx, heart and gonads, the organs are enclosed in a membrane called an epicardium, which is surrounded by the jelly-like mesenchyme. Tunicates begin life in a mobile larval stage that resembles a tadpole, later developing into a barrel-like and usually sedentary adult form.

Tunicates apparently evolved in the early Cambrian period, beginning c 540 million years ago. Despite their simple appearance, tunicates are closely related to vertebrates, which include fish and all land animals with bones.

Contents

Life cycle

Clavelina moluccensis, the bluebell tunicate

Most tunicates are hermaphrodites. The eggs are kept inside their body until they hatch, while sperm is released into the water where it fertilizes other individuals when brought in with incoming water.

Some larval forms appear very much like primitive chordates with a notochord (stiffening rod). Superficially the larva resemble small tadpoles. Some forms have a calcereous spicule that may be preserved as a fossil. They have appeared from the Jurassic to the present, with one proposed Neoproterozoic form, Yarnemia.

The larval stage ends when the tunicate finds a suitable rock to affix to and cements itself in place. The larval form is not capable of feeding, and is only a dispersal mechanism. Many physical changes occur to the tunicate's body, one of the most interesting being the digestion of the cerebral ganglion, which controls movement and is the equivalent of the human brain. From this comes the common saying that the sea squirt "eats its own brain".[2] In some classes, the adults remain pelagic (swimming or drifting in the open sea), although their larvae undergo similar metamorphoses to a higher or lower degree.

Once grown, adults can develop a thick covering, called a tunic, to protect their barrel-shaped bodies from enemies.

During embryonic development, tunicates exhibit "determinate cleavage", where the fate of the cells is set early on with reduced cell numbers and genomes that are rapidly evolving. In contrast, the amphioxus and vertebrates show cell determination relatively late in development and cell cleavage is indeterminate. The genome evolution of amphioxus and vertebrates is also relatively slow.[3]

Feeding

Tunicate colonies of Botrylloides violaceus with oral tentacles at openings of oral siphons visible

Tunicates are suspension feeders. They have two openings in their body cavity: an in-current and an ex-current siphon. The in-current siphon is used to intake food and water, and the ex-current siphon expels waste and water. The tunicate's primary food source is plankton. Plankton gets entangled in the mucus secreted from the endostyle. The tunicate's pharynx is covered by miniature hairs called ciliated cells which allow the consumed plankton to pass down through to the esophagus. Their guts are U-shaped, and their anuses empty directly to the outside environment. Tunicates are also the only animals able to create cellulose.

Tunicate blood is particularly interesting. It contains high concentrations of the transition metal vanadium and vanadium-associated proteins as well as higher than usual levels of lithium. Some tunicates can concentrate vanadium up to a level one million times that of the surrounding seawater. Specialized cells can concentrate heavy metals, which are then deposited in the tunic.

Classification

Tunicates are more closely related to craniates (including hagfish, lampreys, and jawed vertebrates) than to lancelets, echinoderms, hemichordates, Xenoturbella or other invertebrates [4][5][6]. The clade comprising Tunicates and Vertebrates is called Olfactores[7].

The Tunicata contains about 3,000 species, usually divided into the following classes:

Although the traditional classification is followed for now, newer evidence suggests that the Ascidiacea is an artificial group of paraphyletic status [8][9]. The new classification would be:

  • Stolidobranchia ;
  • Aplousobranchia, Phlebobranchia and Thaliacea ;
  • Appendicularia ;
  • Sorberacea would belong somewhere in Ascidiacea, or be in a taxon on its own.

The species Ciona intestinalis and Ciona savignyi have attracted interest in biology for developmental studies. Both species' mitochondrial [10][11] and nuclear [12][13] genomes have been sequenced. Moreover, the nuclear genome of the appendicularian Oikopleura dioica appears to be one of the smallest among metazoans [14].

Sea squirts have become a testing ground in the controversy about the extent to which cross-species gene transfer and hybridization have influenced animal evolution. In 1990, Donald I. Williamson of the University of Liverpool (U.K.) fertilised sea squirt (Ascidia mentula) eggs with sea urchin (Echinus esculentus) sperm resulting in fertile adults that resembled urchins,[15] but Michael W. Hart of Simon Fraser University failed to find sea-squirt DNA in tissue samples from the supposed hybrids.[16] Williamson claims to have repeated the experiment with sea urchin eggs and sea squirt sperm, producing sea urchin larvae which developed into squirt-like juveniles.[17] Michael Syvanen of the University of California has further suggested that sea squirts are themselves descended from a hybrid between a chordate and an ancestor of sea urchins.[18] Like Williamson's, this idea has not yet gained support from embryologists and invertebrate zoologists.

Fossil record

The star-shaped holes (Catellocaula vallata) in this Upper Ordovician bryozoan represent a tunicate preserved by bioimmuration in the bryozoan skeleton.

Undisputed fossils of tunicates are rare. The best known (and earliest) is Shankouclava shankouense from the Lower Cambrian Maotianshan Shale at Shankou village, Anning, near Kunming (South China).[19] There is also a common bioimmuration of a tunicate (Catellocaula vallata) found in Upper Ordovician bryozoan skeletons of the upper midwestern United States.[20]

There is also two enigmatic species from the Ediacaran period - Ausia fenestrata from the Nama Group of Namibia and a second it is new Ausia-like genus from the Onega Peninsula, White Sea of northern Russia. Results of new study have shown possible affinity of these Ediacaran organisms to the ascidians.[21][22] These two organisms lived in the shallow waters of an sea, slightly more than 555-548 million years ago and are likely the oldest evidence of the chordate lineage of metazoans.[22]

A Precambrian fossil known as Yarnemia has been referred to the Urochordata, however this assignment is doubtful. Complete body fossils of tunicates are rare, but in some tunicate families, microscopic spicules are generated which may be preserved as microfossils. Such spicules have occasionally been described from Jurassic and later rocks. Few paleontologists are familiar with them; tunicate spicules may be mistaken for sponge spicules.

Invasive species

Over the past few years, urochordates (notably of the genera Didemnum and Styela) have been invading coastal waters in many countries, and are spreading quickly. These mat-like organisms can smother other sea life, have very few natural predators, and are causing much concern.[23] They form colonies which are yellowish cream in color, and look like thick sponge-like masses that overgrow themselves on stationary objects on the sea floor such as gravel, mollusc shells, and possibly other encrusting species. These colonies are flexible, irregular, long, flat, and often exist as branched outgrowths projected from the surface. Some of the outgrowths result from the colony encrusting worm tubes or other cylindrical objects but many are solid with a firm gelatinous core. The individuals of the colony are called zooids and many zooids with individual siphonal openings cover the surface of the colony.[24]

Transportation of invasive tunicates is usually in the ballast water or on the hulls of ships. Current research indicates that many tunicates previously thought to be indigenous to Europe and the Americas are, in fact, invaders. Some of these invasions may have occurred centuries or even millennia ago. In some areas, tunicates are proving to be a major threat to aquaculture operations.[25][26]

The U.S. Geological Survey, NOAA Fisheries, and the University of Rhode Island are investigating this phenomenon as they have been spotted in 2004 in Georges Bank. They requested that any information or sightings of these invading colonies be reported to USGS to aid in their investigation.[27]

Medical uses

Tunicates contain a host of potentially useful chemical compounds, including:

In the May 2007 issue of The FASEB Journal, researchers from Stanford University showed that tunicates can correct abnormalities over a series of generations, and they suggest that a similar regenerative process may be possible for humans. The mechanisms underlying the phenomenon may lead to insights about the potential of cells and tissues to be reprogrammed and regenerate compromised human organs. Gerald Weissman, editor-in-chief of the journal, said "This study is a landmark in regenerative medicine; the Stanford group has accomplished the biological equivalent of turning a sow's ear into a silk purse and back again."[28]

As food

Various Ascidiacea species are consumed as food around the world.

References

  • Solomon, E., L. Berg, D. Martin. 2002. Biology. Brooks/Cole.
  1. ^ "Gulf Specimen Marine Laboratory: Sea Squirts and Sea Pork". http://www.gulfspecimen.org/SeaSquirts.html. Retrieved 2007-12-10.  
  2. ^ Brainless Fish in Topless Bar - Fast Company
  3. ^ Holland, Linda Z. "Developmental biology: A chordate with a difference." Nature 447.1 (2007): 153-55.
  4. ^ Delsuc F., Brinkmann H., Chourrout D. & Philippe H. (2006). "Tunicates and not cephalochordates are the closest living relatives of vertebrates". Nature 439 (7079): 965–968. PMID 16495997.  
  5. ^ Delsuc F., Tsagkogeorga G., Lartillot N. & Philippe H. (2008). "Additional molecular support for the new chordate phylogeny". Genesis 46 (11): 592–604. PMID 19003928.  
  6. ^ Singh T. R., Tsagkogeorga G., Delsuc F., Blanquart S., Shenkar N., Loya Y., Douzery E. J. & Huchon D. (2009). "Tunicate mitogenomics and phylogenetics: peculiarities of the Herdmania momus mitochondrial genome and support for the new chordate phylogeny". BMC Genomics 10 (1): 534. PMID 19922605. http://www.biomedcentral.com/1471-2164/10/534.  
  7. ^ Jefferies, R. P. S. (1991) in Biological Asymmetry and Handedness (eds Bock G. R. and Marsh J.) pp. 94-127 (Wiley, Chichester).
  8. ^ Zeng L. & Swalla B. J. (2005). "Molecular phylogeny of the protochordates: chordate evolution". Can. J. Zool. 83: 24–33.  
  9. ^ Tsagkogeorga G., Turon X., Hopcroft R. R., Tilak M. K., Feldstein T., Shenkar N., Loya Y., Huchon D., Douzery E. J. & Delsuc F. (2009). "An updated 18S rRNA phylogeny of tunicates based on mixture and secondary structure models". BMC Evol Biol 9: 187. PMID 19656395. http://www.biomedcentral.com/1471-2148/9/187.  
  10. ^ Iannelli F., Pesole G., Sordino P. & Gissi C. (2007). "Mitogenomics reveals two cryptic species in Ciona intestinalis". Trends Genet. 23 (9): 419–422. PMID 17640763.  
  11. ^ Yokobori S., Watanabe Y. & Oshima T. (2003). "Mitochondrial genome of Ciona savignyi (Urochordata, Ascidiacea, Enterogona): Comparison of gene arrangement and tRNA genes with Halocynthia roretzi mitochondrial genome". J. Mol. Evol. 57 (5): 574–587. PMID 14738316.  
  12. ^ Dehal P., Satou Y., Campbell R. K., Chapman J., Degnan B., De Tomaso A., Davidson B., Di Gregorio A., Gelpke M., Goodstein D. M., Harafuji N., Hastings K. E., Ho I., Hotta K., Huang W., Kawashima T., Lemaire P., Martinez D., Meinertzhagen I. A., Necula S., Nonaka M., Putnam N., Rash S., Saiga H., Satake M., Terry A., Yamada L., Wang H. G., Awazu S., Azumi K., Boore J., Branno M., Chin-Bow S., DeSantis R., Doyle S., Francino P., Keys D. N., Haga S., Hayashi H., Hino K., Imai K. S., Inaba K., Kano S., Kobayashi K., Kobayashi M., Lee B. I., Makabe K. W., Manohar C., Matassi G., Medina M., Mochizuki Y., Mount S., Morishita T., Miura S., Nakayama A., Nishizaka S., Nomoto H., Ohta F., Oishi K., Rigoutsos I., Sano M., Sasaki A., Sasakura Y., Shoguchi E., Shin-i T., Spagnuolo A., Stainier D., Suzuki M. M., Tassy O., Takatori N., Tokuoka M., Yagi K., Yoshizaki F., Wada S., Zhang C., Hyatt P. D., Larimer F., Detter C., Doggett N., Glavina T., Hawkins T., Richardson P., Lucas S., Kohara Y., Levine M., Satoh N. & Rokhsar D. S. (2002). "The draft genome of Ciona intestinalis: insights into chordate and vertebrate origins". Science 298 (5601): 2157–2167. PMID 12481130.  
  13. ^ Small K. S., Brudno M., Hill M. M. & Sidow A. (2007). "A haplome alignment and reference sequence of the highly polymorphic Ciona savignyi genome". Genome Biol. 8 (3): R41. PMID 17374142.  
  14. ^ Seo H. C., Kube M., Edvardsen R. B., Jensen M. F., Beck A., Spriet E., Gorsky G., Thompson E. M., Lehrach H., Reinhardt R. & Chourrout D. (2001). "Miniature genome in the marine chordate Oikopleura dioica". Science 294 (5551): 2506–2506. PMID 11752568.  
  15. ^ Williamson, D.I. and Vickers, S.E. (November-December 2007). The Origins of Larvae: Differences in the forms of larvae and adults may reflect fused genomes. American Scientist 95(6): 509-517.
  16. ^ Hart, M.W. (1996). Testing cold fusion of phyla: Maternity in a tunicate × sea urchin hybrid determined from DNA comparisons. Evolution 50(4): 1713–1718.
  17. ^ Williamson, D.I. (in press). Larval transfer: experimental hybrids. In: Margulis, L. and Asikainen, C.A. (editors), Chimeras and Consciousness: Evolution of Sensory Systems. White River Junction, Vermont: Chelsea Green Publishing Co. (Cit. in: Williamson, D.I. and Vickers, S.E. Larval Transfer: A recent evolutionary theory. Ms. submitted to American Scientist.)
  18. ^ Lawton, G. (24 January 2009). Uprooting Darwin's tree. New Scientist 201(2692): 34-39.
  19. ^ Jun-Yuan Chen, Di-Ying Huang, Qing-Qing Peng, Hui-Mei Chi, Xiu-Qiang Wang, and Man Feng (2003). "The first tunicate from the Early Cambrian of South China". Proceedings of the National Academy of Sciences 100: 8314–8318. http://www.pnas.org/content/100/14/8314.full.  
  20. ^ Palmer, T.J. and Wilson, M.A. 1988. Parasitism of Ordovician bryozoans and the origin of pseudoborings. Palaeontology 31: 939-949.
  21. ^ Vickers-Rich P. (2007). "Chapter 4. The Nama Fauna of Southern Africa". In: Fedonkin M.A., Gehling J.G., Grey K., Narbonne G.M., Vickers-Rich P. "The Rise of Animals: Evolution and Diversification of the Kingdom Animalia", Johns Hopkins University Press. pp. 69-87
  22. ^ a b M.A. Fedonkin, P. Vickers Rich, B. Swalla, P. Trusler, M. Hall. (2008). "A Neoproterozoic chordate with possible affinity to the ascidians: New fossil evidence from the Vendian of the White Sea, Russia and its evolutionary and ecological implications". HPF-07 Rise and fall of the Ediacaran (Vendian) biota. International Geological Congress - Oslo 2008.
  23. ^ Squirt Alert
  24. ^ http://sh.nefsc.noaa.gov/tunicate.htm
  25. ^ Marine Nuisance Species
  26. ^ Woods Hole Oceanographic Institution
  27. ^ http://sh.nefsc.noaa.gov/tunicate.htm
  28. ^ Sea Squirt, Heal Thyself: Scientists Make Major Breakthrough In Regenerative Medicine

External links


Simple English

Tunicates
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Subphylum: Urochordata
Giribet et al., 2000
File:Bluebell tunicates Nick
Bluebell tunicates
buds within colonies and along margins of colonies.]]
File:Tunicate colony Nick
Colony of Botryllus.

Tunicates (Sea squirts or Urochordata) are a subphylum of the Chordates. They are filter feeders, living mainly from plankton. The adults are sessile, stuck to rocks. They are called tunicates because the adult form is covered by a leathery tunic. This tunic supports and protects the animal. Many of them are colonial or semi-colonial in their adult stage. They are quite a large group, containing about 3,000 species. The adults live mostly on the sea floor, in the littoral zone.

Contents

Feeding

The sea squirt has two openings in its small body. One opening, called the oral siphon, sucks water into the animal; the other opening, called the atrial siphon, squirts water out of the animal. Inside is a little basket-like sieve which traps food: so these sea squirts are filter feeders. The Sea squirt can close the holes in its siphons, like a drawstring can close the opening in a bag.

Life cycle

When in its larval state, it looks like a tadpole and is sometimes called a tadpole larva. Like many sea creatures, a sea squirt larva looks very different from an adult sea squirt. The larva swims for a short time and then attaches itself to something on the sea floor, like a rock, transforming into its adult form. It usually stays in one place for the rest of its life.

Relationships

Tunicates are more closely related to craniates (hagfish, lampreys, jawed vertebrates) than to lancelets, echinoderms, hemichordates, or other invertebrates.[1][2][3]

Discoveries

Chemical substances which might help fight diseases like cancer or various viruses have been found in some species.

Scientists have also found out that some species can heal some damage done to them, over several generations. A similar process might be possible for humans.[4]

References

Look up Urochordata in Wikispecies, a directory of species
  1. Delsuc F., Brinkmann H., Chourrout D. & Philippe H. (2006). [Expression error: Unexpected < operator "Tunicates and not cephalochordates are the closest living relatives of vertebrates"]. Nature 439 (7079): 965–968. doi:10.1038/nature04336. PMID 16495997. 
  2. Delsuc F., Tsagkogeorga G., Lartillot N. & Philippe H. (2008). [Expression error: Unexpected < operator "Additional molecular support for the new chordate phylogeny"]. Genesis 46 (11): 592–604. doi:10.1002/dvg.20450. PMID 19003928. 
  3. Singh T. R., Tsagkogeorga G., Delsuc F., Blanquart S., Shenkar N., Loya Y., Douzery E. J. & Huchon D. (2009). "Tunicate mitogenomics and phylogenetics: peculiarities of the Herdmania momus mitochondrial genome and support for the new chordate phylogeny". BMC Genomics 10 (1): 534. doi:10.1186/1471-2164-10-534. PMID 19922605. PMC 2785839. http://www.biomedcentral.com/1471-2164/10/534. 
  4. Sea Squirt, heal thyself: scientists make major breakthrough in regenerative medicine
  • Solomon E. Berg L. & Martin D. 2002. Biology. Brooks/Cole.







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