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Aphrodite Worm

Eunice aphroditois (Pallas 1788)

Brief Summary

provided by EOL authors

Eunice aphroditois is a giant marine worm in the speciose polychaete family Eunicidae (which contains over 300 species names; Zanol et al. 2010; Fauchald 1992). One of the world’s longest worms, E. aphroditois is a dramatic sight with different accounts measuring individuals 3-6 meters (10-20 feet) long, their bodies up to 25 mm (1 inch) across.These omnivorous, opportunistic, free-living worms live head-up in burrows just under sand or gravel sediments or in boulders/coral rubble. Five tentacles around their mouth, characteristic of the genus, extend in the water. When it detects prey, the worm springs from its lair, everting its proboscis to expose a fierce pair of mandibles, with which it pulls the prey into its hole.(Video here: https://www.youtube.com/watch?v=GAgWm3G44Aw&feature=player_embedded)

In the 1990s, a giant eunicid worm from the Indo-pacific was photographed and its astonishing feeding behavior documented (as Eunice sp., as even experts could not identify it to species) in an identification manual, Coral Reef Animals of the Indo-Pacific (Gosliner et al. 1996): “...with its 5 pairs of massive, spring loaded jaws, [this species] appears like a frightening apparition from a science fiction movie… This species is a voracious predator.It was observed to feed on a file fish of more than 150 mm in length.When the file fish ventured too close to the worm it emerged slightly from its burrow and seized the fish in its jaws with lightning speed.In an instant, the worm had pulled the fish beneath the sand surface and begun to consume it.”

Originally described from tropical Indo-Pacific waters around Sri Lanka (Pallas 1788), this species is reported around the world, although experts believe this name confounds a multitude of similar-looking giant eunicid worm species.For example, recent work formally distinguished the giant eunicid worm (and commercially important fishing bait species) that inhabits the Mediterranean and Agean Seas as E. roussaei rather than E. aphroditois (Zanol and Bettoso 2006).The difficulties of teasing apart the different species morphologically has made taxonomy, systematics and understanding of the distribution and ecology of species within the genus Eunice very complex. In combination with further study of type material and more collection at type locations, molecular bar coding and molecular phylogenetic characters may prove a helpful tool in the much needed task of defining this and other giant eunicid species more precisely (Schulze 2011; Salazar-Vallejo et al. 2011; Zanol et al 2010).

Gosliner et al. (1996) coined the name Bobbit worm for the Eunice sp. illustrated in their book, associating the worm to the at the time widely-discussed Lorena Bobbit court case.The name simply refers to the sharpness of the worm’s mandibles slicing its prey under attack and the resemblance of the worm to a phallus when holding itself erect to catch prey, not to imply that this worm castrates its mate - which it doesn’t as these worms are broadcast spawners - however this misinterpretation has circulated especially on the web. Just as most giant eunicid worms around the world are ascribed to the species name Eunice aphroditois, most of these worms are also referred to as the Bobbit worm, so rather than as a common name for E. aphroditois, “Bobbit worm” would be better applied generally to all giant eunicid worms (Mah 2013), although these giant worms are not necessarily a monophyletic grouping.

References

  • Fauchald, K. 1992. A review of the geus Eunice (Polychaeta: Eunicidae) based on type material. Smithsonian Contributions to Zoology, 523:422pp
  • Gosliner, T.M., D.W. Behrens and G.C. Williams 1996. Coral Reef Animals of the Indo-Pacific: Animal Life from Africa to Hawaii Exclusive of the Vertebrates. Sea Challengers. ISBN-10: 0930118219.
  • Mah, C. 17 September, 2013. Who Named the Bobbit Worm (Eunice sp.)? And WHAT species is it.. truly?? The Echinoblog. Retrieved June 5, 2015 from http://echinoblog.blogspot.com/2013/09/who-named-bobbit-worm-eunice-sp-and.html.
  • Salazar-Vallejo et al. 2011. Giant Eunicid Polychaetes (Annelida) in shallow tropical and temperate seas. Rev. Biol. Trop. 59-4: 1463-1474.
  • Schulze, 2011. The Bobbit worm dilemma: a case for DNA (Reply to Salazar-Vallejo et al.). Rev. Biol. Trop. (Int. J. Trop. Biol. ISSN-0034-7744) Vol. 59 (4): 1475-1477,
  • Zanol J. and N. Bettoso, 2006. Identity of Eunice roussaei (Eunicidae: Polychaeta: Annelida) from the Adriatic and Mediterranean Seas. J. Mar. Biol. Ass. U.K. (2006), 86, 1017-1024.
  • Zanol, J., K.M. Halanych, T.H. Struck and K. Fauchald, 2010. Phylogeny of the bristle worm family Eunicidae (Eunicida, Annelida) and the phylogenetic utility of noncongruent 16S, COI and 18S in combined analyses. Molecular Phylogenetics and Evolution 55(2):660-676.

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Possible hidden diversity encompassed in E. aphroditois

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Early on in the taxonomic history of the eunicid worms, several specimens from around the world were synonymized into one species name (E. aphroditois).This had the effect of assuming that certain characters had a large amount of variation in the species (e.g. antennal size, articulation of the antennae, type of pectinate chaetae type, maxillae teeth number (Salazar-Vallejo et al. 2011). Thus even though, for example, specimens in Australia had very different branchial patterns and gut contents from those in the Phillipines, they were regarded as the same species.

Salazar-Vallejo et al. 2011 believe that giant eunicid worms photographed from distinct geographies show morphological and behavioral differences that have not as yet been sufficiently analyzed, and historical lumping of these taxa may hide taxonomic diversity.To fully resolve these taxonomic issues requires more understanding of variation (especially of diagnostic characters) in different populations.Because type specimens have been lost over time, and because it is difficult to extract genetic information from embalmed organisms, Salazar-Vallejo et al. 2011) call for resampling at type localities, and using molecular and morphological methods in tandem to characterize possible hidden diversity.These authors identify the following taxa as in particular need of attention: Eunice aphroditois (Sri Lanka), E. gigantea (La Reunion), E. kinbergi (Cape Town), E. longisetis (Bermuda), E. macrobranchia (Cape Town), E. maxima (Naples), E. nigricans (Jamaica), E. purpurea (Adriatic Sea), E. roussaei (Bay of Biscay), E. violacea (Pacific Costa Rica), and E. violaceomaculata (Florida), E. djiboutensis Gravier, 1900 and E. mutabilis Gravier, 1900 (Red Sea).

Some of the variation photographed includes:

Worms from the Phillipines and Indonesia: Dark bands on body; Median antenna same length as peristomal width; Banded anterior appendages; Fusiform peristomal cirri; Branchiae start by chaetiger 5; No white coloration on any anterior chaetigers

Worms from Australia: Body and appendages red in color; Median antennae 2-3 times the width of the peristome; Chaetiger 4 is white; Unknown as to which chaetiger is the start of branchiae.

A worm similar to E. torquata: Body solid red in color; Chaetiger 4 is pure white; Antennae are banded; median antennae 2-3 times the width of the peristome; Peristomal cirri are cirriform and whte; Branchiae start by chaetiger 3, pectinate by chaetiger 9.

Bengal eunicid (Indonesia): Gold and purple body coloring, with lines between segments and longitudinal along body; Chaetiger 4 is white; Solid gold-colored antennae, laterals just longer than the width of the peristome; Peristomial cirri are dark; Branchiae start by chaetiger 7.

Singapore eunicid: dark grey body, with spots mid-body; Chaetigers 4 and 5 have pale bands; Antennae, palps and cirri are pale, with dark tips; Branchiae start by chaetiger 7.

Caribbean eunicid (first form): Dark purple body with fine longitudinal lines; Banded appendages; Peristomal cirri are cirriform, banded; Pectinate branchiae, start at chaetiger 7.

Caribbean eunicid (2nd form): Body dark red with subtle banding on anterior appendages; peristomal cirri are cirriform; Pectinate branchiae, start at chaetiger 9; Younger individuals (and regenerated parts of older individuals) are purple.

Mediterranean Sea species (Eunice gigantea)
Pacific Coast of Central America (E. violacea)
Bay of Biscay/Mediterranean (E. roussaei)
Caribbean (E. violaceomaculata)

(Salazar-Vallejo et al. 2011)

Reference

Salazar-Vallejo, S.I., Carrera-Parra, L.F. and de León-González, A.J. 2011. Giant Eunicid Polychaetes (Annelida) in shallow tropical and temperate seas. Rev. Biol. Trop. 59-4: 1463-1474.

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Comprehensive Description

provided by Smithsonian Contributions to Zoology
Eunice aphroditois (Pallas, 1788)

Nereis aphroditois Pallas, 1788:229–230, pl. 5: figs. 1–7.

Eunice aphroditois.—Cuvier, 1817:525.—Ehlers, 1868:306–310, pl. 15: figs. 23–29.—Fauvel, 1917:215–220, fig. 18 [in part], pl. 7.

Leodice gigantea Lamarck, 1818:322.—Savigny, 1820:49–50.

MATERIAL EXAMINED.—MNHN, Paris, La Réunion, Indian Ocean, coll. M. Carrière, 1910.

COMMENTS ON MATERIAL EXAMINED.—The type material is lost; it came from Sri Lanka; the specimen here described matches the original description closely.

DESCRIPTION.—Specimen posteriorly incomplete, of unknown sex; with 529 setigers; total length 800 mm; maximal width 22 mm at setiger 25; length through setiger 10, 55 mm. Body cylindrical anteriorly, becoming dorsoventrally flattened by setiger 200, but retaining about same width through setiger 400, tapering from setiger 400 setiger to ~10 mm in width at incomplete posterior end.

Prostomium very short, distinctly narrower than peristomium, withdrawn inside nuchal fold, less than as deep as peristomium. Prostomial lobes frontally rounded, dorsally inflated; median sulcus shallow. Eyes not observed. Antennae arranged in a horseshoe, evenly spaced, similar in thickness. Ceratophores ring-shaped in all antennae, without articulations. Ceratostyles thick, digitiform, tapering slightly, without articulations. Antennae to middle of peristomium; right A-II longest, to middle of posterior peristomial ring. Peristomium massive, cylindrical, about twice as wide as prostomium. Separation between rings distinct dorsally and ventrally; anterior ring of total peristomial length. Peristomial cirri to middle of first peristomial ring, thick, slightly inflated basally, without articulations.

Jaws not examined.

Branchiae (Figure 13c, d) present, pectinate, distinctly longer than notopodial cirri, not reduced in mid-body region, erect. Branchiae from setiger 6 to end of fragment. All branchiae pectinate; maximum ~30 filaments in setigers 30–100. Stems thick, erect, tapering, longer than notopodial cirri through setiger 250. Filaments slender, filiform, shorter than notopodial cirri.

Anterior neuropodial acicular lobes truncate to rounded, becoming triangular or slightly conical in far posterior setigers; aciculae emerging at midline. Presetal lobes low, transverse folds. Postsetal lobes forming a collar around acicular lobes, about as high as acicular lobes in anterior and median setigers, projecting beyond acicular lobes in posterior setigers. Anterior ventral cirri thick, tapering from wide, triangular bases, not obviously inflated through setiger 250. Ventral cirri basally inflated in posterior half of fragment. Median and posterior bases first scoop-shaped, becoming triangular welts in last setigers present, retaining short, tapering tips in all setigers. Anterior notopodial cirri basally inflated, tapering to thick tips, becoming very large and very strongly inflated in posterior setigers (Figure 13c), by far dominant parapodial structures in far posterior setigers. All notopodial cirri without articulations.

Limbate setae longer than other setae, slender, marginally finely frayed. Pectinate setae (Figure 13a) in thick fascicles, slender; shafts flattened. Blades tapering, gently furled. Marginal teeth no longer than other teeth, with ~15 teeth. Shafts of compound hooks about as thick as aciculae and subacicular hooks, tapering, marginally smooth; beak indistinct, brass-colored. Appendages not seen. Aciculae paired, with dark brown, rarely black cores and clear sheaths, slender, tapering, distally pointed, usually bent dorsally at tip; cross-section round. Subacicular hooks (Figure 13b) with medium to dark brown cores and clear sheaths, bidentate. Hooks first present from setiger 200, thereafter missing in many setigers, always single (except for replacements). Hooks tapering to very slender, indistinct heads. Proximal teeth larger than distal teeth; both directed distally; both teeth indistinct.

UNKNOWN MORPHOLOGICAL FEATURES.—Features associated with far posterior setigers, pygidium, and anal cirri; jaw structure.

EXPECTED STATE OF SELECTED UNKNOWN FEATURES.—Mx III and IV forming distal arc; Mx VI missing.

CHARACTERS USED IN PREPARATION OF KEY NOT SCORED.—Inappropriate Characters: 56, 60. Unknown Characters: 1, 2, 6, 13, 14, 36–38, 40, 57–59, 69, 70.

ASSUMED STATES FOR PURPOSE OF PREPARING KEY.—37,1; 38,1; 57,1; 58,2; 59,2; 69,1; 70,2.
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bibliographic citation
Fauchald, Kristian. 1992. "A Review of the Genus Eunice (Polychaeta: Eunicidae) Based upon Type Material." Smithsonian Contributions to Zoology. 1-422. https://doi.org/10.5479/si.00810282.523

Comprehensive Description

provided by Smithsonian Contributions to Zoology
Eunice flavopicta Izuka, 1912

Eunice flavopicta Izuka, 1912:121–123, pl. 14: figs. 1–5.
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bibliographic citation
Fauchald, Kristian. 1992. "A Review of the Genus Eunice (Polychaeta: Eunicidae) Based upon Type Material." Smithsonian Contributions to Zoology. 1-422. https://doi.org/10.5479/si.00810282.523

Eunice aphroditois

provided by wikipedia EN

Eunice aphroditois is a benthic bristle worm of warm marine waters. It lives mainly in the Atlantic Ocean, but can also be found in the Indo-Pacific.[1][2] It ranges in length from less than 10 cm (4 in) to 3 m (10 ft).[3] Its iridescent cuticle produces a wide range of colors, from black to purple. This species is an ambush-predator; it hunts by burrowing its whole body in soft sediment on the ocean floor and waiting until its antennae detect prey.[4] It then strikes with its sharp mouthparts.[5] It may also be found among coral reefs.

Eunice aphroditois is commonly known as the sand-striker or bobbit-worm;[6][7][8][9] the latter name is from the John and Lorena Bobbitt case.[10]

Description

Head with antennae

These ambush predators have no eyes and five antennae on their head that are used to sense prey.[11] The body is covered by a hard exoskeleton.[12] The mandibles can be retracted inside the body and are responsible for striking and stunning prey; they are capable of snapping some prey in half.[13] Typically, E. aphroditois ranges from deep purple to black, along with metallic colors. The largest known specimen on record reached 299 centimeters (9.81 ft) in length,[3] making it the longest known member of the polychaete class. Despite these great lengths, the worms are slim, with the body only about 25.5 millimeters (1.00 in) wide.

In an aquarium, showing length
Eunice aphroditois 15533620.jpg

Habitat

This species may be found prowling among the prey-rich environment of coral reefs, where its coloration allows it to blend in and its slim body enables it to hunt in tight places.[13] It inhabits a wide range of other habitats,[14] particularly sandy and muddy sediments, as well as around rocks and sponges.[13] It has been recorded at depths of up to 95 meters.[7]

Diet and interactions

E. aphroditois senses passing prey with its antennae, seizes the prey with its mouth, and drags it into its burrow. To reduce predation risk, some fish engage in mobbing behavior, during which a group of fish will direct jets of water into the worm's burrow to disorient it.[4] This species is not only considered to be a carnivore, feeding on a plethora of species of fish, but it can also be considered an herbivore/omnivore, feeding on algae, as well as a decomposer, feeding on dead and decaying matter.[15]

Ancestral species may have exhibited the same hunting-behavior twenty million years ago, according to fossil-records.[16]

Life-cycle

Like most of the class Polychaeta,[17] E. aphroditois is a sexually-reproducing organism that lacks external reproductive organs. During spawning, female polychaetes produce a pheromone that attracts males and causes them to release sperm; this in turn triggers the female to release eggs into the water, where fertilization occurs.[7] Few offspring survive to adulthood because often, the eggs are eaten by other animals or destroyed.

The lifespan of E. aphroditois is believed to be three to five years.[18]

Regeneration

Like many species of bristle worm, E. aphroditois can also reproduce asexually by splitting into multiple segments, then regenerating body parts such as the head or tail. This enables them to survive being attacked by predators.[19]

Aquaculture

While not commonly kept in aquaculture, individuals of E. aphroditois are occasionally found in home aquaria, where smaller specimens can evade detection by being transported into the tank in live rocks, where they then grow in size.[20] As E. aphroditois hunts fish, it cannot be kept as part of a community tank and should be removed when found, as it will deplete the aquarium's stock by direct predation.[21]

E. aphroditois can be difficult to remove from aquariums due to their abilities to split into new individuals when handled,[19] dig holes into rocks, and curl up and hide in small rocks despite their length.[22]

References

Wikimedia Commons has media related to Eunice aphroditois.
  1. ^ Giangrande, A.; Delos, A. L.; Fraschetti, S.; Musco, L.; Licciano, M.; Terlizzi, A. (2003-12-01). "Polychaete assemblages along a rocky shore on the South Adriatic coast (Mediterranean Sea): patterns of spatial distribution". Marine Biology. 143 (6): 1109–1116. doi:10.1007/s00227-003-1162-0. ISSN 1432-1793. S2CID 85293536.
  2. ^ Fauchald, Kristian. "WoRMS- World Register of Marine Species".
  3. ^ a b Kubota, Shin; Tanase, Hidetomo; Uchida, Hiro'omi (March 2009). "An extraordinarily large specimen of the polychaete worm Eunice aphroditois (Pallas) (Order Eunicea) from Shirahama, Wakayama, central Japan". Kuroshio Biosphere: Bulletin of the Biological Institute on Kuroshio. 5: 9–15. ISSN 1349-2705.
  4. ^ a b Haag-Wackernagel, Daniel; Lachat, Jose (2016-09-12). "Novel mobbing strategies of a fish population against a sessile annelid predator". Scientific Reports. 6: 33187. Bibcode:2016NatSR...633187L. doi:10.1038/srep33187. ISSN 2045-2322. PMC 5018815. PMID 27615670.
  5. ^ Study, Australian Biological Resources (2000). Polychaetes & Allies: The Southern Synthesis. Csiro Publishing. ISBN 9780643065710.
  6. ^ Gosliner, Terrence (1996). Coral Reef Animals of the Indo-Pacific. Sea Challengers. ISBN 0930118219.
  7. ^ a b c "Eunice aphroditois, bobbit worm". www.sealifebase.ca. Retrieved 2019-04-16.
  8. ^ Cormier, Zoe. "Snapping death worms can hide undetected for years". BBC Earth. Retrieved 14 January 2020.
  9. ^ Black, Riley, Giant predatory worms lurked beneath the ancient seafloor, fossils reveal, National Geographic, January 21, 2021
  10. ^ Debelius, Helmut (2001). Asia Pacific Reef Guide: Malaysia, Indonesia, Palau, Philippines, Tropical Japan, China, Vietnam, Thailand. IKAN. p. 305. ISBN 9783925919565.
  11. ^ Glasby, Christopher J.; Read, Geoffrey B. (September 1998). "A chronological review of polychaete taxonomy in New Zealand". Journal of the Royal Society of New Zealand. 28 (3): 347–374. doi:10.1080/03014223.1998.9517570. ISSN 0303-6758.
  12. ^ Paiva, Paulo C.; Fauchald, Kristian; Zanol, Joana (2007-06-01). "A phylogenetic analysis of the genus Eunice (Eunicidae, polychaete, Annelida)". Zoological Journal of the Linnean Society. 150 (2): 413–434. doi:10.1111/j.1096-3642.2007.00302.x. ISSN 0024-4082.
  13. ^ a b c "Eunice aphroditois (Pallas 1788) - Encyclopedia of Life". eol.org.
  14. ^ Fernando, Olivia J. (2011). "EUNICID POLYCHAETES (ANNELIDA) FROM GREAT NICOBAR ISLAND, INDIA: II. ORDER: EUNICIDA" (PDF). Rec. Zool. Surv. India. 111 (Part-4): 29–39.
  15. ^ Eriksson, Mats (2017). "Earth's oldest 'Bobbit worm' – gigantism in a Devonian eunicidan polychaete". Scientific Reports. 7: 43061. Bibcode:2017NatSR...743061E. doi:10.1038/srep43061. PMC 5318920. PMID 28220886.
  16. ^ Pan, Yu-Yen (2021). "The 20-million-year old lair of an ambush-predatory worm preserved in northeast Taiwan". Scientific Reports. 11 (1): 1174. Bibcode:2021NatSR..11.1174P. doi:10.1038/s41598-020-79311-0. PMC 7820589. PMID 33479265.
  17. ^ Gadaleta, M. V.; Matarrese, A.; Tursi, A.; D'Onghia, G.; Giove, A.; Mastrototaro, F. (March 2008). "Benthic diversity of the soft bottoms in a semi-enclosed basin of the Mediterranean Sea". Journal of the Marine Biological Association of the United Kingdom. 88 (2): 247–252. doi:10.1017/S0025315408000726. ISSN 1469-7769. S2CID 85774255.
  18. ^ Holthuis, L.B. (1987). "Résultats des campagnes Musorstom. I et II - Philippines (1976, 1980). Tome 2. In: Mémoires du Muséum National d'Histoire Naturelle. Série A, Zoologie. Tome 133. Décembre 1985. Paris. 525 pp. Price: 350 Fr. To be ordered from: Editions du Muséum National d'Histoire Naturelle, Bibliothèque centrale du Muséum, 38 rue Geoffroy Saint-Hilaire, 75005, Paris". Crustaceana. 53 (3): 320. doi:10.1163/156854087x00466. ISSN 0011-216X.
  19. ^ a b Stanton, Jenny (2013-10-24). "Bobbit worms 'split into sections to regenerate'". SurreyLive. Reach PLC. Retrieved 2023-03-12.
  20. ^ "Bobbit worm found at Woking aquatics store". BBC News. 2013-10-14. Retrieved 2022-09-01.
  21. ^ Callum. "Bobbit Worm". RockNCritters. Retrieved 2022-09-01.
  22. ^ Tung, Liz (2022-11-25). "The Bobbit Worm Chronicles: One man's epic battle against the sea's creepiest crawly". WHYY. WHYY. Retrieved 2023-03-12.
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Eunice aphroditois: Brief Summary

provided by wikipedia EN

Eunice aphroditois is a benthic bristle worm of warm marine waters. It lives mainly in the Atlantic Ocean, but can also be found in the Indo-Pacific. It ranges in length from less than 10 cm (4 in) to 3 m (10 ft). Its iridescent cuticle produces a wide range of colors, from black to purple. This species is an ambush-predator; it hunts by burrowing its whole body in soft sediment on the ocean floor and waiting until its antennae detect prey. It then strikes with its sharp mouthparts. It may also be found among coral reefs.

Eunice aphroditois is commonly known as the sand-striker or bobbit-worm; the latter name is from the John and Lorena Bobbitt case.

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Habitat

provided by World Register of Marine Species
Known from seamounts and knolls

Reference

Stocks, K. 2009. Seamounts Online: an online information system for seamount biology. Version 2009-1. World Wide Web electronic publication.

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