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Ascidiacea
Fossil range: Recent (but see text)
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Halocynthia sp.
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Subphylum: Urochordata
Class: Ascidiacea
Nielsen, 1995
Orders

Ascidiacea (commonly known as the ascidians or sea squirts) is a class in the Urochordata subphylum of sac-like marine invertebrate filter feeders. Ascidians are characterized by a tough outer "tunic" made of the polysaccharide tunicin, as compared to other tunicates which are less rigid.

Ascidians are found all over the world, usually in shallow water with salinities over 2.5%. While members of the Thaliacea and Larvacea swim freely like plankton, sea squirts are sessile animals: they remain firmly attached to substratum such as rocks and shells.

There are 2,300 species of ascidians and three main types: solitary ascidians, social ascidians that form clumped communities by attaching at their bases, and compound ascidians that consist of many small individuals (each individual is called a zooid) forming colonies up to several meters in diameter.

Sea squirts feed by taking in water through the oral siphon. The water enters the mouth and pharynx, flows through mucus-covered gill slits (also called pharyngeal stigmata) into a water chamber called the atrium, then exits through the atrial siphon.

Contents

Life History

Almost all ascidians are hermaphrodites and conspicuous mature ascidians are sessile. Broadly speaking, the ascidians can be divided into species which exist as independent animals (the solitary ascidians) and those which are interdependent (the colonial ascidians). Different species of ascidians can have markedly different reproductive strategies, with colonial forms having mixed modes of reproduction.

Solitary ascidians release many eggs from their atrial siphons; external fertilization in seawater takes place with the coincidental release of sperm from other individuals. A fertilized egg spends 12 hours to a few days developing into a free-swimming tadpole larva, which then takes several more hours/days to settle and metamorphose into a juvenile. The larva selects and settles on appropriate surfaces using receptors sensitive to light, orientation to gravity, and tactile stimuli. When its anterior end touches a surface, papillae (small, finger-like nervous projections) secrete an adhesive for attachment. Adhesive secretion prompts an irreversible metamorphosis: various organs (such as the larval tail and fins) are lost while others rearrange to their adult positions, the pharynx enlarges, and organs called ampullae grow from the body to permanently attach the animal to the substratum. The siphons of the juvinile ascidian become orientated to optimise current flow through the feeding apparatus. Sexual maturity can be reached in as little as a few weeks. Most solitary ascidians live between 1–3 years.

Colonial ascidians reproduce both asexually and sexually. Colonies can survive for decades. An ascidian colony consists of individual elements called zooids. Zooids within a colony are usually genetically identical and some have a shared circulation. Different colonial ascidian species produce sexually derived offspring by one of two dispersal strategies- Colonial species are either broadcast spawners (long-range dispersal) or philopatric (very short-range dispersal). Broadcast spawners release sperm and ova into the water column and fertilization occurs near to the parent colonies. Resultant zygotes develop into microscopic larvae that may be carried great distances by oceanic currents. The larvae of sessile forms which survive eventually settle and complete maturation on the substratum- then they may bud asexually to form a colony of zooids.

The picture is more complicated for the philopatrically dispersed ascidians: sperm from a nearby colony (or from a zooid of the same colony) enter the pharyngeal siphon and fertilization takes place within the atrium. Embryos are then brooded within the atrium where embryonic development takes place: this results in macroscopic tadpole-like larvae. When mature, these larvae exit the atrial siphon of the adult and then settle close to the parent colony (often within meters). The combined effect of short sperm range and philopatric larval dispersal results in local population structures of closely related individuals/inbred colonies. Generations of colonies which are restricted in dispersal are thought to accumulate adaptions to local conditions, thereby providing advantages over newcomers.

Trauma or predation often results in fragmentation of a colony into subcolonies. Subsequent zooid replication can lead to coalescence and circulatory fusion of the subcolonies. Closely related colonies which are proximate to each other may also fuse if they coalesce and if they are histocompatible. Ascidians were among the first animals to be able to immunologically recognize self from non-self as a mechanism to prevent unrelated colonies from fusing to them and parasitizing them.

Fertilization

Sea squirt eggs are surrounded by a fibrous vitelline coat and a layer of follicle cells that produce sperm-attracting substances. In fertilization, the sperm passes through the follicle cells and binds to glycosides on the vitelline coat. The sperm's mitochondria are left behind as the sperm enters and drives through the coat; this translocation of the mitochondria might provide the necessary force for penetration. The sperm swims through the perivitelline space, finally reaching the egg plasma membrane and entering the egg. This prompts rapid modification of the vitelline coat, through processes such as the egg's release of glycosidase into the seawater, so no more sperm can bind and polyspermy is avoided. After fertilization, free calcium ions are released in the egg cytoplasm in waves, mostly from internal stores. The temporary large increase in calcium concentration prompts the physiological and structural changes of development.

The dramatic rearrangement of egg cytoplasm following fertilization, called ooplasmic segregation, determines the dorsoventral and anteroposterior axes of the embryo. There are at least three types of sea squirt egg cytoplasm: ectoplasm containing vesicles and fine particles, endoderm containing yolk platelets, and myoplasm containing pigment granules, mitochondria, and endoplasmic reticulum. In the first phase of ooplasmic segregation, the myoplasmic actin-filament network contracts to rapidly move the peripheral cytoplasm (including the myoplasm) to the vegetal pole, which marks the dorsal side of the embryo. In the second phase, the myoplasm moves to the subequatorial zone and extends into a crescent, which marks the future posterior of the embryo. The ectoplasm with the zygote nucleus ends up at the animal hemisphere while the endoplasm ends up in the vegetal hemisphere.

Ecology

The exceptional filtering capability of adult sea squirts causes them to accumulate pollutants that may be toxic to embryos and larvae as well as impede enzyme function in adult tissues. This property has made some species sensitive indicators of pollution.

Over the last few hundred years, most of the world's harbors have been invaded by non-native sea squirts that have clung to ship hulls or to introduced organisms such as oysters and seaweed. Several factors, including quick attainment of sexual maturity, tolerance of a wide range of environments, and a lack of predators, allow sea squirt populations to grow rapidly. Unwanted populations on docks, ship hulls, and farmed shellfish cause significant economic problems, and sea squirt invasions have disrupted the ecosystem of several natural sub-tidal areas by smothering native animal species.

A sea squirt (Polycarpa aurata) being used as a substrate for a nudibranch's (Nembrotha lineolata) egg spiral.

Sea squirts are the natural prey of many animals, including nudibranchs, flatworms, molluscs, rock crabs, sea stars, fish, birds, and sea otters. They are also eaten by humans in many parts of the world, including Japan, Korea, Chile, and Europe (where they are sold under the name “sea violet”). As chemical defenses, many sea squirts intake and maintain an extremely high concentration of vanadium in the blood, have a very low pH of the tunic due to acid in easily-ruptured bladder cells, and (or) produce secondary metabolites harmful to predators and invaders. Some of these metabolites are toxic to cells and are of potential use in pharmaceuticals.

Central Nervous System

The ascidian central nervous system is formed from a neural plate that is rolled into a neural tube. The number of cells designated to the central nervous system is very small. The neural tube is composed of the sensory vesicle, the neck, the visceral or tail ganglion, and the caudal nerve cord. The anteroposterior regionalization of the neural tube in ascidians is comparable to that in vertebrates.[1]

Fossil record

Despite bearing distinctive aragonite spicules, the fossil record of the sea squirts is almost entirely lacking – a dubious Silurian specimen being the only contender.[2]

Uses

Culinary

Various Ascidiacea are used as food. Sea pineapple (Halocynthia roretzi) is cultivated in Japan (hoya, maboya) and Korea (meongge) and, when eaten raw, has been described by Lonely Planet as tasting like "rubber dipped in ammonia". The peculiar flavor is attributed to an unsaturated alcohol called cynthiaol.

The Korean fish stew agujjim traditionally contains the tunicate Styela clava. [3] According to the LA Weekly, "they are actually farmed in parts of Korea, and sea squirt bibimbap is a specialty of Geojae-do island, not far from Masan."

Microcosmus sabatieri and several similar species from the Mediterranean Sea are eaten in France (figue de mer, violet), Italy (limone di mare, uova di mare) and Chile (piure), consumed both raw and used as ingredients in seafood stews like bouillabaisse.

Pyura stolonifera is known as cunjevoi in Australia. This was once used as a food source by Aboriginal people living around Botany Bay, but is now used mainly for fishing bait. Note: the word "cunjevoi" is also used for two species of rainforest plant, at least one of which is toxic to humans.

Model organisms for research

Ernst Haeckel's interpretation of several ascidians. From Kunstformen der Natur, 1904.

A number of factors make sea squirts good models for studying the fundamental developmental processes of chordates, such as cell-fate specification. The embryonic development of sea squirts is simple, rapid, and easily manipulated. Because each embryo contains relatively few cells, complex processes can be studied at the cellular level, while remaining in the context of the whole embryo. The embryo's transparency is ideal for fluorescent imaging and its maternally-derived proteins are naturally pigmented, so cell lineages are easily labeled, allowing scientists to visualize embryogenesis from beginning to end.

Sea squirts are also valuable because of their unique evolutionary position: as an approximation of ancestral chordates, they can provide insight into the link between chordates and ancestral non-chordate deuterostomes, as well as the origination of vertebrates from simple chordates.[4] The sequenced genomes of the related sea squirts Ciona intestinalis and Ciona savignyi are small and easily manipulated; comparisons with the genomes of other organisms such as flies, nematodes, pufferfish and mammals provides valuable information regarding chordate evolution. A collection of over 480,000 cDNAs have been sequenced and are available to support further analysis of gene expression, which is expected to provide information about complex developmental processes and regulation of genes in vertebrates. Gene expression in embryos of sea squirts can be conveniently inhibited using Morpholino oligos[5].

References

  1. ^ Ikuta, Tetsuro, and Hidetoshi Saiga. "Organization of Hox genes in ascidians: Present, past, and future." Developmental Dynamics 233.2 (2005): 382-89.
  2. ^ Where Are All the Fossil Sea Squirts?
    1. M. E. Brookfield
    2. Micropaleontology, Vol. 34, No. 3 (1988), pp. 277-283

External links

Gallery


Wiktionary

Up to date as of January 14, 2010

Definition from Wiktionary, a free dictionary

Contents

Translingual

Etymology

Proper noun

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Ascidiacea

  1. a taxonomic class, within subphylum Urochordata - very many solitary or colonial sessile tunicates
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See also

  • Aplousobranchia
  • Phlebobranchia
  • Sorberacea
  • Stolidobranchia

Wikispecies

Up to date as of January 23, 2010

From Wikispecies

Ascidiacea sp.

Taxonavigation

Main Page
Cladus: Eukaryota
Supergroup: Unikonta
Cladus: Opisthokonta
Regnum: Animalia
Subregnum: Eumetazoa
Cladus: Bilateria
Cladus: Nephrozoa
Cladus: Deuterostomia
Phylum: Chordata
Subphylum: Urochordata
Classis: Ascidiacea
Ordines: Enterogona - Pleurogona

References

  • Monniot, F. 2009: Some ascidians from Indonesian marine lakes (Raja Ampat Islands, West Papua). Zootaxa, 2106: 13-40. Abstract & excerpt

Vernacular names

Česky: Sumky
Dansk: Søpunge
Deutsch: Seescheiden
Ελληνικά: Ασκίδια
English: Ascidiacea
Français: Ascidies
Italiano: Ascidie
Македонски: Асцидии
Nederlands: Zakpijp
日本語: ホヤ綱
Polski: Żachwy
中文: 海鞘纲
Wikimedia Commons For more multimedia, look at Ascidiacea on Wikimedia Commons.







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