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Echiura

The Echiura, or spoon worms, are a small group of marine animals. 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.

Echiura
Temporal range: Upper Carboniferous–Recent[1]
Urechis caupo
Scientific classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Annelida
Clade: Pleistoannelida
Clade: Sedentaria
Subclass: Echiura
Newby, 1940[2][3]
Subdivision
Echiurus

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 edit

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 edit

Spoon worms vary in size from the giant Ikeda taenioides, nearly 2 m (7 ft) long with its proboscis extended, to the minute Lissomyema, measuring just 1 cm (0.4 in).[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 (59 in) long while the body is only 40 centimetres (16 in). 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 most 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]

Distribution and habitat edit

 
Ochetostoma erythrogrammon

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 3,000 m (10,000 ft).[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 edit

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 Maldives
 
Bonellia 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]

Urechidae, another group of tube-dwellers, has become filter feeders.[23] 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 nutrient-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.[24] 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.[25]

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.[26]

Reproduction edit

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]

Fertilization is internal in the sexual dimorphic order Bonelliida, which has dwarf males living inside the female. Members of the order Echiurida have external fertilization and are sexual monomorphic.[27][28]

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 15 cm (6 in) in body length, excluding the proboscis, but the males are only 1 to 3 mm (0.04 to 0.12 in) long, and spend their adult lives within the uterus of the female.[15]

As food edit

 
Spoon worms at a market in South Korea

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.[29] They are also eaten as a fermented product known as gaebul-jeot.[30]

List of families edit

According to the World Register of Marine Species:[3]

References edit

  1. ^ a b 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.
  2. ^ a b "Spoon Worm". Britannica.com. Retrieved 9 March 2019.
  3. ^ a b Tanaka, Masaatsu (2017). "Echiura". WoRMS. World Register of Marine Species. Retrieved 17 February 2019.
  4. ^ Zhang, Z.-Q. (2011). "Animal biodiversity: An introduction to higher-level classification and taxonomic richness" (PDF). Zootaxa. 3148: 7–12. doi:10.11646/zootaxa.3148.1.3. Archived (PDF) from the original on 2022-10-09.
  5. ^ Tanaka, Masaatsu (2017). "Echiurus echiurus (Pallas, 1766)". WoRMS. World Register of Marine Species. Retrieved 17 February 2019.
  6. ^ Banta, W.C.; Rice, M.E. (1970). (PDF). Proceedings of the International Symposium on the Biology of the Sipunculata and Echiura. 11. Archived from the original (PDF) on 2012-03-12. Retrieved 2019-02-17.
  7. ^ Elsberry, Wesley R. (10 June 2006). "Phylum Echiura". Online Zoologists. Retrieved 17 February 2019.
  8. ^ 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. PMID 18322464. S2CID 4397099.
  9. ^ 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. PMID 18692145.
  10. ^ 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. PMID 21368831. S2CID 4428998.
  11. ^ Struck, T. H.; Schult, N.; Kusen, T.; Hickman, E.; Bleidorn, C.; McHugh, D.; Halanych, K. M. (2007). "Annelid phylogeny and the status of Sipuncula and Echiura". BMC Evolutionary Biology. 7: 57. doi:10.1186/1471-2148-7-57. PMC 1855331. PMID 17411434.
  12. ^ Tilic, Ekin; Lehrke, Janina; Bartolomaeus, Thomas; Colgan, Donald James (3 March 2015). "Homology and Evolution of the Chaetae in Echiura (Annelida)". PLOS ONE. 10 (3): e0120002. Bibcode:2015PLoSO..1020002T. doi:10.1371/journal.pone.0120002. PMC 4348511. PMID 25734664.
  13. ^ "Introduction to the Echiura". UC Museum of Paleontology. Retrieved 7 March 2019.
  14. ^ a b c d e f Ruppert, Edward E.; Fox, Richard, S.; Barnes, Robert D. (2004). Invertebrate Zoology, 7th edition. Cengage Learning. pp. 490–495. ISBN 978-81-315-0104-7.{{cite book}}: CS1 maint: multiple names: authors list (link)
  15. ^ a b c d e f g h Barnes, Robert D. (1982). Invertebrate Zoology. Philadelphia, PA: Holt-Saunders International. pp. 870–873. ISBN 0-03-056747-5.
  16. ^ Toonen, Rob (2012). . Reefkeeper's Guide to Invertebrate Zoology. Archived from the original on 26 August 2012. Retrieved 10 November 2012.
  17. ^ a b c d e f Walls, Jerry G. (1982). Encyclopedia of Marine Invertebrates. TFH Publications. pp. 262–267. ISBN 0-86622-141-7.
  18. ^ a b Felty Light, Sol (1954). Intertidal Invertebrates of the Central California Coast. University of California Press. p. 108. ISBN 9780520007505. Retrieved 30 November 2011.
  19. ^ Conn, H.W. (1886). "Life history of Thalassema mellita". Stud. Biol. Lab. Johns Hopkins Univ.: 1884–1887.
  20. ^ a b Stull, Janet K.; Haydock, C.Irwin; Montagne, David E. (1986). "Effects of Listriolobus pelodes (Echiura) on coastal shelf benthic communities and sediments modified by a major California wastewater discharge". Estuarine, Coastal and Shelf Science. 22 (1): 1–17. Bibcode:1986ECSS...22....1S. doi:10.1016/0272-7714(86)90020-X.
  21. ^ Shipley, Arthur Everett (1911). "Echiuroidea" . In Chisholm, Hugh (ed.). Encyclopædia Britannica. Vol. 08 (11th ed.). Cambridge University Press. pp. 882–883.
  22. ^ Cowles, Dave (2005). "Echiurus echiurus subspecies alaskanus Fisher, 1946". Invertebrates of the Salish Sea. Retrieved 18 February 2019.
  23. ^ The food composition of the symbiotic crab Pinnixa rathbunae Sakai, 1934 (Brachyura: Pinnotheridae) from burrows of the spoon worm Urechis unicinctus (von Drasche, 1881 (Echiurida: Urechidae) in Vostok Bay of the Sea of Japan
  24. ^ Chuang, S. H. (1962). "Feeding Mechanism of the Echiuroid, Ochetostoma erythrogrammon Leuckart & Rueppell, 1828". Biological Bulletin. 123 (1): 80–85. doi:10.2307/1539504. JSTOR 1539504.
  25. ^ van der Land, Jacob (2004). "Echiuroidea". WoRMS. World Register of Marine Species. Retrieved 30 November 2011.
  26. ^ Tallent, L.G. (1976). "Food habits of the leopard shark, Triakis semifasciata, in Elkhorn Slough, Monterey Bay, California". California Fish and Game. 62 (4): 286–298.
  27. ^ A comprehensive molecular phylogeny of spoon worms (Echiura, Annelida): Implications for morphological evolution, the origin of dwarf males, and habitat shifts
  28. ^ Molecular Phylogeny of Echiuran Worms (Phylum: Annelida) Reveals Evolutionary Pattern of Feeding Mode and Sexual Dimorphism
  29. ^ Brown, Nicholas; Eddy, Steve (2015). Echinoderm Aquaculture. Wiley. p. 60. ISBN 978-1-119-00585-8.
  30. ^ Kun-Young Park; Dae Young Kwon; Ki Won Lee; Sunmin Park (2018). Korean Functional Foods: Composition, Processing and Health Benefits. CRC Press. p. 232. ISBN 978-1-351-64369-6.
  31. ^ Tanaka, Masaatsu (2017). "Bonelliida". WoRMS. World Register of Marine Species. Retrieved 9 March 2019.
  32. ^ Tanaka, Masaatsu (2017). "Echiurida". WoRMS. World Register of Marine Species. Retrieved 9 March 2019.

External links edit

  •   Media related to Echiura at Wikimedia Commons
  •   Data related to Echiura at Wikispecies

echiura, spoon, worms, small, group, marine, animals, once, treated, separate, phylum, they, considered, belong, annelida, annelids, typically, have, their, bodies, divided, into, segments, echiurans, have, secondarily, lost, their, segmentation, majority, ech. The Echiura or spoon worms are a small group of marine animals 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 EchiuraTemporal range Upper Carboniferous Recent 1 PreꞒ Ꞓ O S D C P T J K Pg N Urechis caupo Scientific classification Domain Eukaryota Kingdom Animalia Phylum Annelida Clade Pleistoannelida Clade Sedentaria Subclass EchiuraNewby 1940 2 3 Subdivision Order Bonelliida Family Bonelliidae Family Ikedidae Order Echiurida Family Echiuridae Family Thalassematidae Family Urechidae Echiurus 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 Contents 1 Taxonomy and evolution 2 Anatomy 3 Distribution and habitat 4 Behaviour 5 Reproduction 6 As food 7 List of families 8 References 9 External linksTaxonomy and evolution editThe 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 editSpoon worms vary in size from the giant Ikeda taenioides nearly 2 m 7 ft long with its proboscis extended to the minute Lissomyema measuring just 1 cm 0 4 in 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 59 in long while the body is only 40 centimetres 16 in 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 most 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 Distribution and habitat edit nbsp Ochetostoma erythrogrammon 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 3 000 m 10 000 ft 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 editA 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 nbsp Characteristic forked proboscis of an echiurian worm in the Maldives nbsp Bonellia 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 Urechidae another group of tube dwellers has become filter feeders 23 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 nutrient 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 24 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 25 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 26 Reproduction editEchiurans 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 Fertilization is internal in the sexual dimorphic order Bonelliida which has dwarf males living inside the female Members of the order Echiurida have external fertilization and are sexual monomorphic 27 28 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 15 cm 6 in in body length excluding the proboscis but the males are only 1 to 3 mm 0 04 to 0 12 in long and spend their adult lives within the uterus of the female 15 As food edit nbsp Spoon worms at a market in South Korea 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 29 They are also eaten as a fermented product known as gaebul jeot 30 List of families editAccording to the World Register of Marine Species 3 suborder Bonelliida 31 family Bonelliidae Lacaze Duthiers 1858 family Ikedidae Bock 1942 suborder Echiurida 32 family Echiuridae Quatrefages 1847 family Thalassematidae Forbes amp Goodsir 1841 family Urechidae Fisher amp Macginitie 1928 nbsp A worm of the family Bonelliidae nbsp Ochetostoma erythrogrammon family Echiuridae nbsp Arhynchite hayaoi family Thalassematidae nbsp Urechis unicinctus family UrechidaeReferences edit a b 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 a b Spoon Worm Britannica com Retrieved 9 March 2019 a b Tanaka Masaatsu 2017 Echiura WoRMS World Register of Marine Species Retrieved 17 February 2019 Zhang Z Q 2011 Animal biodiversity An introduction to higher level classification and taxonomic richness PDF Zootaxa 3148 7 12 doi 10 11646 zootaxa 3148 1 3 Archived PDF from the original on 2022 10 09 Tanaka Masaatsu 2017 Echiurus echiurus Pallas 1766 WoRMS World Register of Marine Species Retrieved 17 February 2019 Banta W C Rice M E 1970 A restudy of the Middle Cambrian Burgess Shale fossil worm Ottoia prolifica PDF Proceedings of the International Symposium on the Biology of the Sipunculata and Echiura 11 Archived from the original PDF on 2012 03 12 Retrieved 2019 02 17 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 Sorensen 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 PMID 18322464 S2CID 4397099 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 PMID 18692145 Struck T H Paul C Hill N Hartmann S Hosel 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 PMID 21368831 S2CID 4428998 Struck T H Schult N Kusen T Hickman E Bleidorn C McHugh D Halanych K M 2007 Annelid phylogeny and the status of Sipuncula and Echiura BMC Evolutionary Biology 7 57 doi 10 1186 1471 2148 7 57 PMC 1855331 PMID 17411434 Tilic Ekin Lehrke Janina Bartolomaeus Thomas Colgan Donald James 3 March 2015 Homology and Evolution of the Chaetae in Echiura Annelida PLOS ONE 10 3 e0120002 Bibcode 2015PLoSO 1020002T doi 10 1371 journal pone 0120002 PMC 4348511 PMID 25734664 Introduction to the Echiura UC Museum of Paleontology Retrieved 7 March 2019 a b c d e f Ruppert Edward E Fox Richard S Barnes Robert D 2004 Invertebrate Zoology 7th edition Cengage Learning pp 490 495 ISBN 978 81 315 0104 7 a href Template Cite book html title Template Cite book cite book a CS1 maint multiple names authors list link a b c d e f g h Barnes Robert D 1982 Invertebrate Zoology Philadelphia PA Holt Saunders International pp 870 873 ISBN 0 03 056747 5 Toonen Rob 2012 Part 6 Phylum Sipuncula and Phylum Annelida Reefkeeper s Guide to Invertebrate Zoology Archived from the original on 26 August 2012 Retrieved 10 November 2012 a b c d e f Walls Jerry G 1982 Encyclopedia of Marine Invertebrates TFH Publications pp 262 267 ISBN 0 86622 141 7 a b Felty Light Sol 1954 Intertidal Invertebrates of the Central California Coast University of California Press p 108 ISBN 9780520007505 Retrieved 30 November 2011 Conn H W 1886 Life history of Thalassema mellita Stud Biol Lab Johns Hopkins Univ 1884 1887 a b Stull Janet K Haydock C Irwin Montagne David E 1986 Effects of Listriolobus pelodes Echiura on coastal shelf benthic communities and sediments modified by a major California wastewater discharge Estuarine Coastal and Shelf Science 22 1 1 17 Bibcode 1986ECSS 22 1S doi 10 1016 0272 7714 86 90020 X Shipley Arthur Everett 1911 Echiuroidea In Chisholm Hugh ed Encyclopaedia Britannica Vol 08 11th ed Cambridge University Press pp 882 883 Cowles Dave 2005 Echiurus echiurus subspecies alaskanus Fisher 1946 Invertebrates of the Salish Sea Retrieved 18 February 2019 The food composition of the symbiotic crab Pinnixa rathbunae Sakai 1934 Brachyura Pinnotheridae from burrows of the spoon worm Urechis unicinctus von Drasche 1881 Echiurida Urechidae in Vostok Bay of the Sea of Japan Chuang S H 1962 Feeding Mechanism of the Echiuroid Ochetostoma erythrogrammon Leuckart amp Rueppell 1828 Biological Bulletin 123 1 80 85 doi 10 2307 1539504 JSTOR 1539504 van der Land Jacob 2004 Echiuroidea WoRMS World Register of Marine Species Retrieved 30 November 2011 Tallent L G 1976 Food habits of the leopard shark Triakis semifasciata in Elkhorn Slough Monterey Bay California California Fish and Game 62 4 286 298 A comprehensive molecular phylogeny of spoon worms Echiura Annelida Implications for morphological evolution the origin of dwarf males and habitat shifts Molecular Phylogeny of Echiuran Worms Phylum Annelida Reveals Evolutionary Pattern of Feeding Mode and Sexual Dimorphism Brown Nicholas Eddy Steve 2015 Echinoderm Aquaculture Wiley p 60 ISBN 978 1 119 00585 8 Kun Young Park Dae Young Kwon Ki Won Lee Sunmin Park 2018 Korean Functional Foods Composition Processing and Health Benefits CRC Press p 232 ISBN 978 1 351 64369 6 Tanaka Masaatsu 2017 Bonelliida WoRMS World Register of Marine Species Retrieved 9 March 2019 Tanaka Masaatsu 2017 Echiurida WoRMS World Register of Marine Species Retrieved 9 March 2019 External links edit nbsp Media related to Echiura at Wikimedia Commons nbsp Data related to Echiura at Wikispecies Retrieved from https en 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