The Echiura, or spoon worms, are a small group of marineanimals. Once treated as a separate phylum, they are now considered to belong to Annelida. Annelids typically have their bodies divided into segments, but echiurans have secondarily lost their segmentation. The majority of echiurans live in burrows in soft sediment in shallow water, but some live in rock crevices or under boulders, and there are also deep sea forms. More than 230 species have been described.[4] Spoon worms are cylindrical, soft-bodied animals usually possessing a non-retractable proboscis which can be rolled into a scoop-shape to feed. In some species the proboscis is ribbon-like, longer than the trunk and may have a forked tip. Spoon worms vary in size from less than a centimetre in length to more than a metre.
Most are deposit feeders, collecting detritus from the sea floor. Fossils of these worms are seldom found and the earliest known fossil specimen is from the Upper Carboniferous (Pennsylvanian).
Taxonomy and evolution
The spoonworm Echiurus echiurus was first described by the Prussian naturalist Peter Simon Pallas in 1766; he placed it in the earth worm genus Lumbricus.[5] In the mid-nineteenth century Echiura was placed, alongside Sipuncula and Priapulida, in the now defunct class Gephyrea (meaning a "bridge") in Annelida, because it was believed that they provided a link between annelids and holothurians.[6] In 1898, Sedgwick raised the sipunculids and priapulids to phylum status but considered Echiuroids to be a class of the Annelida.[7] During the early 1900s, a biologist named Jon Stanton Whited devoted his working life to study the echiurans and classify many of its different species. In 1940, after the American marine biologist W. W. Newby had studied the embryology and development of Urechis caupo, he raised the group to phylum status.[2]
They are now universally considered to represent derived annelid worms; as such, their ancestors were segmented worms but echiurans have secondarily lost their segmentation.[8][9][10][11] Their presumed sister group is the Capitellidae.[12]
Having no hard parts, these worms are seldom found as fossils. The oldest known unambiguous example is Coprinoscolex ellogimus from the Mazon Creek fossil beds in Illinois, dating back to the Middle Pennsylvanian period. This exhibits a proboscis, cigar‐shaped body and convoluted gut, and shows that already at that time, echiurans were unsegmented and were essentially similar to modern forms.[1] However, U-shaped burrow fossils that could be Echiuran have been found dating back to the Cambrian.[13]
Anatomy
Spoon worms vary in size from the giant Ikeda taenioides, nearly 2m (7ft) long with its proboscis extended, to the minute Lissomyema, measuring just 1cm (0.4in).[14] Their bodies are generally cylindrical with two wider regions separated by a narrower region. There is a large extendible, scoop-shaped proboscis in front of the mouth which gives the animals their common name. This proboscis resembles that of peanut worms but it cannot be retracted into the body. It houses a brain and may be homologous to the prostomium of other annelids.[15] The proboscis has rolled-in margins and a groove on the ventral surface. The distal end is sometimes forked. The proboscis can be very long; in the case of the Japanese species Ikeda taenioides, the proboscis can be 150 centimetres (59in) long while the body is only 40 centimetres (16in). Even smaller species like Bonellia can have a proboscis a metre (yard) long. The proboscis is used primarily for feeding. Respiration takes place through the proboscis and the body wall, with some larger species also using cloacal irrigation. In this process, water is pumped into and out of the rear end of the gut through the anus.[14][16]
Compared with other annelids, echiurans have relatively few setae (bristles). In most species, there are just two, located on the underside of the body just behind the proboscis, and often hooked. In others, such as Echiurus, there are also further setae near the posterior end of the animal. Unlike other annelids, adult echiurans have no trace of segmentation.[15] Most echiurans are a dull grey or brown but a few species are more brightly coloured, such as the translucent green Listriolobus pelodes.[17]
The body wall is muscular. It surrounds a large coelom which leads to a long looped intestine with an anus at the rear tip of the body.[18] The intestine is highly coiled, giving it a considerable length in relation to the size of the animal. A pair of simple or branched diverticula are connected to the rectum. These are lined with numerous minute ciliated funnels that open directly into the body cavity, and are presumed to be excretory organs.[15] The proboscis has a small coelomic cavity separated from the main coelom by a septum.[14]
Echiurans do not have a distinct respiratory system, absorbing oxygen through the body wall of both the trunk and proboscis, and through the cloaca in Urechis.[14] Although some species lack a blood vascular system, where it is present, it resembles that of other annelids. The blood is essentially colourless, although some haemoglobin-containing cells are present in the coelomic fluid of the main body cavity. There can be anywhere from one to over a hundred metanephridia for excreting nitrogenous waste, which typically open near the anterior end of the animal.[15] The nervous system consists of a brain near the base of the proboscis, and a ventral nerve cord running the length of the body. Aside from the absence of segmentation, this is a similar arrangement to that of other annelids. Echiurans do not have any eyes or other distinct sense organs,[15] but the proboscis is presumed to have a tactile sensory function.[17]
Echiurans are exclusively marine and the majority of species live in the Atlantic Ocean. They are mostly infaunal, occupying burrows in the seabed, either in the lower intertidal zone or the shallow subtidal (e.g. the genera Echiurus, Urechis, and Ikeda).[17] Others live in holes in coral heads, and in rock crevices. Some are found in deep waters including at abyssal depths; in fact more than half the 70 species in Bonelliidae live below 3,000m (10,000ft).[14] They often congregate in sediments with high concentrations of organic matter. One species, Lissomyema mellita, which lives off the southeastern coast of the US, inhabits the tests (exoskeleton) of dead sand dollars. When the worm is very small, it enters the test and later becomes too large to leave.[19]
In the 1970s, the spoon worm Listriolobus pelodes was found on the continental shelf off Los Angeles in numbers of up to 1,500 per square metre (11 square feet) near sewage outlets.[20] The burrowing and feeding activities of these worms churned up and aerated the sediment and promoted a balanced ecosystem with a more diverse fauna than would otherwise have existed in this heavily polluted area.[20]
Behaviour
A spoon worm can move about on the surface by extending its proboscis and grasping some object before pulling its body forward. Some worms, such as Echiurus, can leave the substrate entirely, swimming by use of the proboscis and contractions of the body wall.[21]
Digging behaviour has been studied in Echiurus echiurus. When burrowing, the proboscis is raised and folded backwards and plays no part in the digging process. The front of the trunk is shaped into a wedge and pushed forward, with the two anterior chaetae (hooked chitinous bristles) being driven into the sediment. Next the rear end of the trunk is drawn forward and the posterior chaetae anchor it in place. These manoeuvres are repeated and the worm slowly digs its way forwards and downwards. It takes about forty minutes for the worm to disappear from view. The burrow descends diagonally and then flattens out, and it may be a metre or so long before ascending vertically to the surface.[22]
Characteristic forked proboscis of an echiurian worm in the MaldivesBonellia viridis, female
Spoon worms are typically detritivores, extending the flexible and mobile proboscis and gathering organic particles that are within reach. Some species can expand the proboscis by ten times its contracted length. The proboscis is moved by the action of cilia on the lower (ventral) surface "creeping" it forward. When food particles are encountered, the sides of the proboscis curl inward to form a ciliated channel.[14]
A worm such as Echiurus, living in the sediment, extends its proboscis from the rim of its burrow with the ventral side on the substrate. The surface of the proboscis is well equipped with mucus glands to which food particles adhere. The mucus is bundled into boluses by cilia and these are passed along the feeding groove by cilia to the mouth. The proboscis is periodically withdrawn into the burrow and later extended in another direction.[17]
Urechis, another tube-dweller, has a different method of feeding on detritus. It has a short proboscis and a ring of mucus glands at the front of its body. It expands its muscular body wall to deposit a ring of mucus on the burrow wall then retreats backwards, exuding mucus as it goes and spinning a mucus net. It then draws water through the burrow by peristaltic contractions and food particles stick to the net. When this is sufficiently clogged up, the spoon worm moves forward along its burrow devouring the net and the trapped particles. This process is then repeated and in a detritus-rich area may take only a few minutes to complete. Large particles are squeezed out of the net and eaten by other invertebrates living commensally in the burrow. These typically include a small crab, a scale worm and often a fish lurking just inside the back entrance.[17]
Ochetostoma erythrogrammon obtains its food by another method. it has two vertical burrows connected by a horizontal one. Stretching out its proboscis across the substrate it shovels material into its mouth before separating the edible particles. It can lengthen the proboscis dramatically while exploring new areas and periodically reverses its orientation in the burrow so as to use the back entrance to feed.[23] Other spoon worms live concealed in rock crevices, empty gastropod shells, sand dollar tests and similar places, extending their proboscises into the open water to feed.[18] Some are scavengers or detritivores, while others are interface grazers and some are suspension feeders.[24]
While the proboscis of a burrowing spoon worm is on the surface it is at risk of predation by bottom-feeding fish. In some species, the proboscis will autotomise (break off) if attacked and the worm will regenerate a proboscis over the course of a few weeks.[17] In a study in California, one of the most commonly found dietary items of the leopard shark was found to be the tube-dwelling innkeeper worm (Urechis caupo) which it extracted from the sediment by suction.[25]
Reproduction
Echiurans are dioecious, with separate male and female individuals. The gonads are associated with the peritoneal membrane lining the body cavity, into which they release the gametes. The sperm and eggs complete their maturation in the body cavity, before being stored in genital sacs, which are specialised metanephridia. At spawning time, the genital sacs contract and the gametes are squeezed into the water column through pores on the worm's ventral surface. Fertilization is external.[15]
Fertilized eggs hatch into free-swimming trochophore larvae. In some species, the larva briefly develops a segmented body before transforming into the adult body plan, supporting the theory that echiurans evolved from segmented ancestors resembling more typical annelids.[15]
The species Bonellia viridis, also remarkable for the possible antibiotic properties of bonellin, the green chemical in its skin, is unusual for its extreme sexual dimorphism. Females are typically 15cm (6in) in body length, excluding the proboscis, but the males are only 1 to 3mm (0.04 to 0.12in) long, and spend their adult lives within the uterus of the female.[15]
Spoon worms are eaten in East and Southeast Asia. In South Korea fat innkeeper worms (Urechis unicinctus) are known as gaebul (개불). These worms are much prized and are often available at markets and stalls, chopped up and served raw in combination with raw sea cucumber, sea squirt and sea urchin, dressed with chili sauce and soy sauce.[26] They are also eaten as a fermented product known as gaebul-jeot.[27]
The Sipuncula or Sipunculida is a class containing about 162 species of unsegmented marine annelid worms. Sipuncula was once considered a phylum, but was demoted to a class of Annelida, based on recent molecular work.
Nemertea is a phylum of animals also known as ribbon worms or proboscis worms, consisting of 1300 known species. Most ribbon worms are very slim, usually only a few millimeters wide, although a few have relatively short but wide bodies. Many have patterns of yellow, orange, red and green coloration. The foregut, stomach and intestine run a little below the midline of the body, the anus is at the tip of the tail, and the mouth is under the front. A little above the gut is the rhynchocoel, a cavity which mostly runs above the midline and ends a little short of the rear of the body. All species have a proboscis which lies in the rhynchocoel when inactive but everts to emerge just above the mouth to capture the animal's prey with venom. A highly extensible muscle in the back of the rhynchocoel pulls the proboscis in when an attack ends. A few species with stubby bodies filter feed and have suckers at the front and back ends, with which they attach to a host.
Polychaeta is a paraphyletic class of generally marine annelid worms, commonly called bristle worms or polychaetes. Each body segment has a pair of fleshy protrusions called parapodia that bear many bristles, called chaetae, which are made of chitin. More than 10,000 species are described in this class. Common representatives include the lugworm and the sandworm or clam worm Alitta.
Urechis unicinctus, known as the fat innkeeper worm or penis fish, is a species of marine spoon worm in East Asia. It is found in Bohai Gulf of China and off the Korean and Hokkaido coasts. It is not to be confused with a closely related species, Urechis caupo, which occurs on the western coast of North America and shares common names. The body is about 10–30 centimetres (3.9–11.8 in) long, cylindrical in shape and yellowish-brown in color. On the surface of the body there are many small papillae.
Bonellia viridis, the green spoonworm, is a marine worm noted for displaying exceptional sexual dimorphism and for the biocidal properties of a pigment in its skin.
Leeches are segmented parasitic or predatory worms that comprise the subclass Hirudinea within the phylum Annelida. They are closely related to the oligochaetes, which include the earthworm, and like them have soft, muscular segmented bodies that can lengthen and contract. Both groups are hermaphrodites and have a clitellum, but leeches typically differ from the oligochaetes in having suckers at both ends and in having ring markings that do not correspond with their internal segmentation. The body is muscular and relatively solid, and the coelom, the spacious body cavity found in other annelids, is reduced to small channels.
Phoronids are a small phylum of marine animals that filter-feed with a lophophore, and build upright tubes of chitin to support and protect their soft bodies. They live in most of the oceans and seas, including the Arctic Ocean but excluding the Antarctic Ocean, and between the intertidal zone and about 400 meters down. Most adult phoronids are 2 cm long and about 1.5 mm wide, although the largest are 50 cm long.
Gephyrea is a now-dismantled class of marine worms, containing the three modern taxa Echiura, Sipuncula, and Priapulida. Also Sternaspis, the first described genus in the family Sternaspidae, was at some point assumed to be related to Echiura and therefore included in the Gephyrea. This class was not monophyletic. Priapulida are now considered a distinct phylum among Ecdysozoa, while the other two taxa are classified as Annelids. The word was created by Quatrefages from the Greek γέφυρα (géphura) 'bridge', because these animals seemed intermediate between Annelids and Holothurians.
Listriolobus pelodes is a species of marine spoon worm. It is found in shallow seas in the North East Pacific off the coast of California. It lives in a burrow in soft sediments.
Hediste diversicolor, commonly known as a ragworm, is a polychaete worm in the family Nereididae. It lives in a burrow in the sand or mud of beaches and estuaries in intertidal zones in the north Atlantic. This species is used in research, but its classification is in dispute; in the literature, it is often classified as Nereis diversicolor. Its specific name "diversicolor" refers to the fact that its colour changes from brown to green as the breeding season approaches.
The annelids, also known as the segmented worms, are a large phylum, with over 22,000 extant species including ragworms, earthworms, and leeches. The species exist in and have adapted to various ecologies – some in marine environments as distinct as tidal zones and hydrothermal vents, others in fresh water, and yet others in moist terrestrial environments.
Polydora ciliata is a species of annelid worm in the family Spionidae, commonly known as a bristleworm. It is a burrowing worm and is found in the northeastern Atlantic Ocean and some other parts of the world.
Bonelliidae is a family of marine worms noted for being sexually dimorphic, with males being tiny in comparison with the females. They occupy burrows in the seabed in many parts of the world's oceans, often at great depths.
Metabonellia is a genus of marine spoon worms in the family Bonelliidae. It is a monotypic genus and Metabonellia haswelli is the only species. It is commonly known as the green spoon worm and is found in shallow waters around Australia.
Urechis caupo is a species of spoon worm in the family Urechidae, commonly known as the innkeeper echiuran, the fat innkeeper worm, the innkeeper worm, or the penis fish. It is found in shallow water on the west coast of North America, between southern Oregon and Baja California, where it forms a U-shaped burrow in the sediment and feeds on plankton using a mucus net.
Ochetostoma erythrogrammon is a species of spoon worm in the family Thalassematidae. It is found in shallow water in the Atlantic Ocean, the Mediterranean Sea, and the Indian and Pacific Oceans, burrowing in soft sediment.
Ikedidae is a family of spoon worms in the suborder Bonelliida. It is a monotypic family, the only genus being Ikeda. These worms burrow into soft sediment on the seabed.
Ikeda taenioides is a species of spoon worm in the family Ikedidae. It is native to the northern Pacific Ocean where it is found in the subtidal waters around Japan.
Maxmuelleria lankesteri is a species of spoon worm in the family Bonelliidae. It is found in the North Atlantic Ocean. It burrows into soft sediment on the seabed, mostly in deep water.
Maldanidae is a family of more than 200 species of marine polychaetes commonly known as bamboo worms or maldanid worms. They belong to the order Capitellida, in the phylum Annelida. They are most closely related to family Arenicolidae, and together form the clade Maldanomorpha.
References
1 2 Jones, D.; Thompson, I. D. A. (1977). "Echiura from the Pennsylvanian Essex Fauna of northern Illinois". Lethaia. 10 (4): 317. doi:10.1111/j.1502-3931.1977.tb00627.x.
↑ Elsberry, Wesley R. (10 June 2006). "Phylum Echiura". Online Zoologists. Retrieved 17 February 2019.
↑ Dunn, C. W.; Hejnol, A.; Matus, D. Q.; Pang, K.; Browne, W. E.; Smith, S. A.; Seaver, E.; Rouse, G. W.; Obst, M.; Edgecombe, G. D.; Sørensen, M. V.; Haddock, S. H. D.; Schmidt-Rhaesa, A.; Okusu, A.; Kristensen, R. M. B.; Wheeler, W. C.; Martindale, M. Q.; Giribet, G. (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. PMID18322464. S2CID4397099.
↑ Bourlat, S.; Nielsen, C.; Economou, A.; Telford, M. (2008). "Testing the new animal phylogeny: A phylum level molecular analysis of the animal kingdom". Molecular Phylogenetics and Evolution. 49 (1): 23–31. doi:10.1016/j.ympev.2008.07.008. PMID18692145.
↑ Struck, T. H.; Paul, C.; Hill, N.; Hartmann, S.; Hösel, C.; Kube, M.; Lieb, B.; Meyer, A.; Tiedemann, R.; Purschke, G. N.; Bleidorn, C. (2011). "Phylogenomic analyses unravel annelid evolution". Nature. 471 (7336): 95–98. Bibcode:2011Natur.471...95S. doi:10.1038/nature09864. PMID21368831. S2CID4428998.
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