Tunicate

Tunicate
Temporal range: Cambrian stage 3–Recent
Sea Tulips, Pyura spinifera
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Subphylum: Tunicata
Giribet et al., 2000
Classes

Tunicates, previously known as Urochordata, or urochordates, are members of the Tunicata, a subphylum of the phylum Chordata. They are marine filter feeders with a saclike morphology. In their respiration and feeding they take in water through an incurrent (or inhalant) siphon and expel the filtered water through an excurrent (or exhalant) siphon. Most adult tunicates are sessile and attached to rocks or similarly suitable surfaces on the ocean floor; others such as salps, doliolids and pyrosomes swim in the pelagic zone as adults. Various species are commonly known as sea squirts[1] or sea pork.[2]

The Tunicata apparently evolved in the early Cambrian period. Despite their simple appearance, they are a sister subphylum to the Vertebrata.

Contents

General physiology, morphology, and development

Like other chordates, tunicates have a notochord during their early development, but by the time they have completed their larval stages they have lost all myomeric segmentation throughout the body. As members of the Chordata they are true Coelomata with endoderm, ectoderm and mesoderm, but they do not develop very clear coelomic body-cavities if any at all. Whether they do or not, by the end of their larval development all that remain are the pericardial, renal, and gonadal cavities of the adults. Except for the heart, gonads, and pharynx (or branchial sac), 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. A minority of species, those in the Larvacea, retain the general larval form throughout life, but most Tunicata very rapidly settle down and attach themselves to a suitable surface, later developing into a barrel-like and usually sedentary adult form. The Thaliacea however, are pelagic throughout their lives. and their life cycles may be complex, as for example in the Salpida.

Tunicates lack kidney-like metanephridial organs, but make do with a less elaborate nitrogenous excretory system. The typical renal organ is a mass of large clear-walled vesicles that occupy the rectal loop, and the structure has no duct. Each vesicle is a remnant of a part of the primitive coelom, and its cells extract nitrogenous waste matter from circulating blood. They accumulate the wastes inside the vesicles as urates and do not have any obvious means of disposing of the material during the life of the animal.

Tunicates are unusual among animals in that they produce a large fraction of their tunic and some other structures in the form of cellulose. Cellulose production in animals is so inconspicuous that some sources deny its presence outside plants, but for some time now it has been known to occur in the dermis of mammals. However, the Tunicata are unique in their scale of application and production of the material. When in 1845 Carl Schmidt first announced the presence in the test of some Ascidians of a substance very similar to cellulose, he called it "tunicine", but it now is recognised as cellulose rather than any alternative substance.[3][4][5][6]

Feeding

Most tunicates are suspension feeders, capturing suspended particles and plankton by filtering sea water through their siphons via their pharyngeal slits, but some, such as the Megalodicopia hians, are marine sit-and-wait predators.

Tunicates have two openings in their body cavity: an incurrent and an excurrent siphon. The incurrent siphon is takes in water plus any food it contains, and the excurrent siphon expels wastes plus sieved water. The primary food source for most tunicates is plankton that gets entangled in mucus secreted from the endostyle. The tunicate's pharynx, or branchial sac, is lined with ciliated epithelium. The action of the cilia passes food particles and plankton down to the esophagus and also passes the stream of water from the inhalant to the exhalant siphon. The gut is U-shaped and also ciliated, and the anus opens into the dorsal or cloacal part of the peribranchial cavity near the atrial aperture, where the constant stream of water carries wastes to the exterior.

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.

Taxonomy

Urochordata is a junior synonym of the name Tunicata which was established by Lamarck in 1816. Balfour introduced the name Urochordata in 1881 in order to emphasize the affinity of the group to other chordates but this was unnecessary as Tunicata was a pre-existing and perfectly satisfactory name. The name Tunicata is almost invariably used to refer to this group of organisms in scientific works.[7] It is accepted as valid by the World Register of Marine Species [8] and by ITIS, the Integrated Taxonomic Information System.[9]

Classification

Tunicates are more closely related to craniates (including hagfish, lampreys, and jawed vertebrates) than to lancelets, echinoderms, hemichordates, Xenoturbella or other invertebrates.[10][11][12] The clade comprising Tunicates and Vertebrates is called Olfactores.[13]

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.[14][15] The new classification would be:

The species Ciona intestinalis and Ciona savignyi have attracted interest in biology for developmental studies. Both species' mitochondrial[16][17] and nuclear[18][19] genomes have been sequenced. Moreover, the nuclear genome of the appendicularian Oikopleura dioica appears to be one of the smallest among metazoans.[20]

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,[21] but Michael W. Hart of Simon Fraser University failed to find sea-squirt DNA in tissue samples from the supposed hybrids.[22] 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.[23] On the other hand, Syvanen and Ducore of the University of California have suggested that sea squirts descended from a hybrid between a chordate and a likely extinct protostome ancestor at a time before the diversification of round worms and arthropods. This study also examined whether there was evidence of a sea urchin/tunicate hybridization event that could possibly explain the distribution of genes in modern sea squirts—none could be seen.[24][25]

Life cycle

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. They swim with a tail, and may have a simple eye, or ocellus, and balancing organ, or statolith.[26] Some forms have a calcareous 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 form ends when the tunicate finds a suitable rock to affix to and cements itself in place. The larval form is not capable of feeding, though it may have a digestive system,[26] 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".[27] 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.

In growing to adulthood, tunicates develop a thick protective covering, called a tunic, or test, around their barrel-shaped bodies.[28]

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.[29]

Fossil record

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).[30] There is also a common bioimmuration of a tunicate (Catellocaula vallata) found in Upper Ordovician bryozoan skeletons of the upper midwestern United States.[31]

There are also two enigmatic species from the Ediacaran period - Ausia fenestrata from the Nama Group of Namibia and a second 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.[32][33] These two organisms lived in the shallow waters of a sea, slightly more than 555-548 million years ago and are likely the oldest evidence of the chordate lineage of metazoans.[33]

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.[34] 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.[35]

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.[36][37]

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 United States Geological Survey to aid in their investigation.[35]

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."[38]

As food

Various Ascidiacea species are consumed as food around the world.

References

  1. ^ Branch, G.M. Griffiths, C.L. Branch, M.L. Beckley, L.E. (2010). Two oceans : a guide to the marine life of Southern Africa. Cape Town: Struik Nature. ISBN 9781770077720. 
  2. ^ "Gulf Specimen Marine Laboratory: Sea Squirts". http://www.gulfspecimen.org/SeaSquirts.html. Retrieved 2007-12-10. 
  3. ^ Harmer, Sir Sidney Frederic; Shipley, Arthur Everett et alia: The Cambridge natural history Volume 7, Hemichordata, Ascidians, Amphioxus and Fishes Macmillan Company 1904
  4. ^ Euichi Hirose, Keisuke Nakashima, Atsuo Nishino. Is there intracellular cellulose in the appendicularian tail epidermis? Communicative & Integrative Biology 4:6, 768-771; November/December 2011; Landes Bioscience
  5. ^ Hall, D. A. Saxl, Hedwig. Studies of Human and Tunicate Cellulose and of their Relation to Reticulin. Proc. R. Soc. Lond. B 1961 155, 202-217 doi: 10.1098/rspb.1961.0066
  6. ^ Levine, Michael S. Transposon-mediated insertional mutagenesis revealed the functions of animal cellulose synthase. University of California, Berkeley. http://www.pnas.org/content/102/42/15134.full 2005
  7. ^ "Ascidian News". Depts.washington.edu. http://depts.washington.edu/ascidian/AN54.html. Retrieved 2011-12-07. 
  8. ^ Tunicata World Register of Marine Species. Retrieved 2011-11-12.
  9. ^ Tunicata Lamarck, 1816 Integrated Taxonomic Information System. Retrieved 2011-11-12.
  10. ^ 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. doi:10.1038/nature04336. PMID 16495997. 
  11. ^ Delsuc F., Tsagkogeorga G., Lartillot N. & Philippe H. (2008). "Additional molecular support for the new chordate phylogeny". Genesis 46 (11): 592–604. doi:10.1002/dvg.20450. PMID 19003928. 
  12. ^ 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: 534. doi:10.1186/1471-2164-10-534. PMC 2785839. PMID 19922605. http://www.biomedcentral.com/1471-2164/10/534. 
  13. ^ Jefferies, R. P. S. (1991) in Biological Asymmetry and Handedness (eds Bock G. R. and Marsh J.) pp. 94-127 (Wiley, Chichester).
  14. ^ Zeng L. & Swalla B. J. (2005). "Molecular phylogeny of the protochordates: chordate evolution". Can. J. Zool. 83: 24–33. doi:10.1139/z05-010. 
  15. ^ 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. doi:10.1186/1471-2148-9-187. PMC 2739199. PMID 19656395. http://www.biomedcentral.com/1471-2148/9/187. 
  16. ^ Iannelli F., Pesole G., Sordino P. & Gissi C. (2007). "Mitogenomics reveals two cryptic species in Ciona intestinalis". Trends Genet. 23 (9): 419–422. doi:10.1016/j.tig.2007.07.001. PMID 17640763. 
  17. ^ 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. doi:10.1007/s00239-003-2511-9. PMID 14738316. 
  18. ^ 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. doi:10.1126/science.1080049. PMID 12481130. 
  19. ^ 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. doi:10.1186/gb-2007-8-3-r41. PMC 1868934. PMID 17374142. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1868934. 
  20. ^ 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. doi:10.1126/science.294.5551.2506. PMID 11752568. 
  21. ^ 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.
  22. ^ 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.
  23. ^ 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.)
  24. ^ Syvanen,M and Ducore,J (2010) Whole genome comparisons reveals a possible chimeric origin for a major metazoan assemblage. J. Biol. Systems. 18: 261 - 275.
  25. ^ Lawton, G. (24 January 2009). Uprooting Darwin's tree. New Scientist 201(2692): 34-39.
  26. ^ a b mol smith. "Microscopy-uk.org.uk". Microscopy-uk.org.uk. http://www.microscopy-uk.org.uk/mag/indexmag.html?http://www.microscopy-uk.org.uk/mag/artdec00/tunicp1.html. Retrieved 2011-12-07. 
  27. ^ "Brainless Fish in Topless Bar". Fast Company. 1999-04-30. http://www.fastcompany.com/magazine/24/cdu.html. Retrieved 2011-12-07. 
  28. ^ Martinez, Andrew J.; Martinez, Candace Storm. Marine Life of the North Atlantic. Publisher: Aqua Quest Publications 2011. ISBN-13: 978-1881652359
  29. ^ Holland, Linda Z. "Developmental biology: A chordate with a difference." Nature 447.1 (2007): 153-55.
  30. ^ 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 (14): 8314–8318. doi:10.1073/pnas.1431177100. PMC 166226. PMID 12835415. http://www.pnas.org/content/100/14/8314.full. 
  31. ^ Palmer, T.J. and Wilson, M.A. 1988. Parasitism of Ordovician bryozoans and the origin of pseudoborings. Palaeontology 31: 939-949.
  32. ^ 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
  33. ^ 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.
  34. ^ Squirt Alert
  35. ^ a b "SH.nefsc.noaa.gov". SH.nefsc.noaa.gov. 2004-11-19. http://sh.nefsc.noaa.gov/tunicate.htm. Retrieved 2011-12-07. 
  36. ^ "Marine Nuisance Species". Woodshole.er.usgs.gov. http://woodshole.er.usgs.gov/project-pages/stellwagen/didemnum/index.htm. Retrieved 2011-12-07. 
  37. ^ Woods Hole Oceanographic Institution
  38. ^ "Sea Squirt, Heal Thyself: Scientists Make Major Breakthrough In Regenerative Medicine". Sciencedaily.com. 2007-04-24. http://www.sciencedaily.com/releases/2007/04/070424093740.htm. Retrieved 2011-12-07. 

External links