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Polychaete

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Polychaetes
Temporal range: Cambrian (or earlier?) – present
"A variety of marine worms": plate from Das Meer by M. J. Schleiden (1804–1881)
"A variety of marine worms": plate from Das Meer by M. J. Schleiden (1804–1881)
Scientific classificationEdit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Annelida
Class: Polychaeta
Grube, 1850
Groups included
Cladistically included but traditionally excluded taxa

Chaetopteridae[1]

Polychaeta (/ˌpɒlɪˈkiːtə/) is a paraphyletic[1] class of generally marine annelid worms, commonly called bristle worms or polychaetes (/ˈpɒlɪˌkiːts/). 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 (Arenicola marina) and the sandworm or clam worm Alitta.

Polychaetes as a class are robust and widespread, with species that live in the coldest ocean temperatures of the abyssal plain, to forms which tolerate the extremely high temperatures near hydrothermal vents. Polychaetes occur throughout the Earth's oceans at all depths, from forms that live as plankton near the surface, to a 2- to 3-cm specimen (still unclassified) observed by the robot ocean probe Nereus at the bottom of the Challenger Deep, the deepest known spot in the Earth's oceans.[2] Only 168 species (less than 2% of all polychaetes) are known from fresh waters.[3]

Description

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Polychaetes are segmented worms, generally less than 10 cm (4 in) in length, although ranging at the extremes from 1 mm (0.04 in) to 3 m (10 ft), in Eunice aphroditois. They can sometimes be brightly coloured, and may be iridescent or even luminescent. Each segment bears a pair of paddle-like and highly vascularized parapodia, which are used for movement and, in many species, act as the worm's primary respiratory surfaces. Bundles of bristles, called chaetae, project from the parapodia.[4]

However, polychaetes vary widely from this generalized pattern, and can display a range of different body forms. The most generalised polychaetes are those that crawl along the bottom, but others have adapted to many different ecological niches, including burrowing, swimming, pelagic life, tube-dwelling or boring, commensalism, and parasitism, requiring various modifications to their body structures.

The head, or prostomium, is relatively well developed, compared with other annelids. It projects forward over the mouth, which therefore lies on the animal's underside. The head normally includes two to four pair of eyes, although some species are blind. These are typically fairly simple structures, capable of distinguishing only light and dark, although some species have large eyes with lenses that may be capable of more sophisticated vision,[4] including the Alciopids' complex eyes which rival cephalopod and vertebrate eyes.[5][6]

Many species show bioluminescence; eight families have luminous species.[7][8]

The head also includes a pair of antennae, tentacle-like palps, and a pair of pits lined with cilia, known as "nuchal organs". These latter appear to be chemoreceptors, and help the worm to seek out food.[4]

Internal anatomy and physiology

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General anatomy of a polychaete
Phyllodoce rosea

The outer surface of the body wall consists of a simple columnar epithelium covered by a thin cuticle. Underneath this, in order, are a thin layer of connective tissue, a layer of circular muscle, a layer of longitudinal muscle, and a peritoneum surrounding the body cavity. Additional oblique muscles move the parapodia. In most species the body cavity is divided into separate compartments by sheets of peritoneum between each segment, but in some species it is more continuous.

The mouth of polychaetes is located on the peristomium, the segment behind the prostomium, and varies in form depending on their diets, since the group includes predators, herbivores, filter feeders, scavengers, and parasites. In general, however, they possess a pair of jaws and a pharynx that can be rapidly everted, allowing the worms to grab food and pull it into their mouths. In some species, the pharynx is modified into a lengthy proboscis. The digestive tract is a simple tube, usually with a stomach part way along.

The smallest species, and those adapted to burrowing, lack gills, breathing only through their body surfaces. Most other species have external gills, often associated with the parapodia.

A simple but well-developed circulatory system is usually present. The two main blood vessels furnish smaller vessels to supply the parapodia and the gut. Blood flows forward in the dorsal vessel, above the gut, and returns down the body in the ventral vessel, beneath the gut. The blood vessels themselves are contractile, helping to push the blood along, so most species have no need of a heart. In a few cases, however, muscular pumps analogous to a heart are found in various parts of the system. Conversely, some species have little or no circulatory system at all, transporting oxygen in the coelomic fluid that fills their body cavities.[4]

The blood may be colourless, or have any of three different respiratory pigments. The most common of these is haemoglobin, but some groups have haemerythrin or the green-coloured chlorocruorin, instead.

The nervous system consists of a single or double ventral nerve cord running the length of the body, with ganglia and a series of small nerves in each segment. The brain is relatively large, compared with that of other annelids, and lies in the upper part of the head. An endocrine gland is attached to the ventral posterior surface of the brain, and appears to be involved in reproductive activity. In addition to the sensory organs on the head, photosensitive eye spots, statocysts, and numerous additional sensory nerve endings, most likely involved with the sense of touch, also occur on the body.[4]

Polychaetes have a varying number of protonephridia or metanephridia for excreting waste, which in some cases can be relatively complex in structure. The body also contains greenish "chloragogen" tissue, similar to that found in oligochaetes, which appears to function in metabolism, in a similar fashion to that of the vertebrate liver.[4]

The cuticle is constructed from cross-linked fibres of collagen and may be 200 nm to 13 mm thick. Their jaws are formed from sclerotised collagen, and their setae from sclerotised chitin.[9]

Ecology

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The Pompeii worm lives at great depths by hydrothermal vents at temperatures up to 80 °C
Hesiocaeca methanicola lives at great depths on methane ice
The cold seep tube worm Lamellibrachia can live over 250 years
The predatory Bobbit worm

Polychaetes are predominantly marine, but many species also live in freshwater, and a few in terrestrial environments.[10] They are extremely variable in both form and lifestyle, and include a few taxa that swim among the plankton or above the abyssal plain. Most burrow or build tubes in the sediment, and some live as commensals. A few species, roughly 80 (less than 0.5% of species), are parasitic.[11][12] These include both ectoparasites and endoparasites. Ectoparasitic polychaetes feed on skin, blood, and other secretions, and some are adapted to bore through hard, usually calcerous surfaces, such as the shells of mollusks.[12] These "boring" polychaetes may be parasitic, but may be opportunistic or even obligate symbionts (commensals).[13][12][11]

The mobile forms (Errantia) tend to have well-developed sense organs and jaws, while the stationary forms (Sedentaria) lack them, but may have specialized gills or tentacles used for respiration and deposit or filter feeding, e.g., fanworms. Underwater polychaetes have eversible mouthparts used to capture prey.[14][self-published source?] A few groups have evolved to live in terrestrial environments, like Namanereidinae with many terrestrial species, but are restricted to humid areas. Some have even evolved cutaneous invaginations for aerial gas exchange.

Notable polychaetes

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  • One notable polychaete, the Pompeii worm (Alvinella pompejana), is endemic to the hydrothermal vents of the Pacific Ocean. Pompeii worms are among the most heat-tolerant complex animals known.
  • A recently discovered genus, Osedax, includes a species nicknamed the "bone-eating snot flower".[15]
  • Another remarkable polychaete is Hesiocaeca methanicola, which lives on methane clathrate deposits.
  • Lamellibrachia luymesi is a cold seep tube worm that reaches lengths of over 3 m and may be the most long-lived annelid, being over 250 years old.
  • A still unclassified multilegged predatory polychaete worm was identified only by observation from the underwater vehicle Nereus at the bottom of the Challenger Deep, the greatest depth in the oceans, near 10,902 m (35,768 ft) in depth. It was about an inch long visually, but the probe failed to capture it, so it could not be studied in detail.[16]
  • The Bobbit worm (Eunice aphroditois) is a predatory species that can achieve a length of 3 m (10 ft)), with an average diameter of 25 mm (1 in).
  • Dimorphilus gyrociliatus has the smallest known genome of any annelid. The species shows extreme sexual dimorphism. Females measure ~1 mm long and have simplified bodies containing six segments, a reduced coelom, and no appendages, parapodia, or chaetae. The males are only 50 μm long and consist of just a few hundred cells. They lack a digestive system and have just 68 neurons, and only live for roughly a week.[17][18]

Reproduction

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Most polychaetes have separate sexes, rather than being hermaphroditic. The most primitive species have a pair of gonads in every segment, but most species exhibit some degree of specialisation. The gonads shed immature gametes directly into the body cavity, where they complete their development. Once mature, the gametes are shed into the surrounding water through ducts or openings that vary between species, or in some cases by the complete rupture of the body wall (and subsequent death of the adult). A few species copulate, but most fertilize their eggs externally.

The fertilized eggs typically hatch into trochophore larvae, which float among the plankton, and eventually metamorphose into the adult form by adding segments. A few species have no larval form, with the egg hatching into a form resembling the adult, and in many that do have larvae, the trochophore never feeds, surviving off the yolk that remains from the egg.[4]

However, some polychaetes exhibit remarkable reproductive strategies. Some species reproduce by epitoky. For much of the year, these worms look like any other burrow-dwelling polychaete, but as the breeding season approaches, the worm undergoes a remarkable transformation as new, specialized segments begin to grow from its rear end until the worm can be clearly divided into two halves. The front half, the atoke, is asexual. The new rear half, responsible for breeding, is known as the epitoke. Each of the epitoke segments is packed with eggs and sperm and features a single eyespot on its surface. The beginning of the last lunar quarter is the cue for these animals to breed, and the epitokes break free from the atokes and float to the surface. The eye spots sense when the epitoke reaches the surface and the segments from millions of worms burst, releasing their eggs and sperm into the water.[19]

A similar strategy is employed by the deep sea worm Syllis ramosa, which lives inside a sponge. The rear ends of the worm develop into "stolons" containing the eggs or sperm; these stolons then become detached from the parent worm and rise to the sea surface, where fertilisation takes place.[20]

Fossil record

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Stem-group polychaete fossils are known from the Sirius Passet Lagerstätte, a rich, sedimentary deposit in Greenland tentatively dated to the late Atdabanian (early Cambrian). The oldest found is Phragmochaeta canicularis.[21] Many of the more famous Burgess Shale organisms, such as Canadia, may also have polychaete affinities. Wiwaxia, long interpreted as an annelid,[22] is now considered to represent a mollusc.[23][24] An even older fossil, Cloudina, dates to the terminal Ediacaran period; this has been interpreted as an early polychaete, although consensus is absent.[25][26]

Being soft-bodied organisms, the fossil record of polychaetes is dominated by their fossilized jaws, known as scolecodonts, and the mineralized tubes that some of them secrete.[27] Most important biomineralising polychaetes are serpulids, sabellids, and cirratulids. Polychaete cuticle does have some preservation potential; it tends to survive for at least 30 days after a polychaete's death.[9] Although biomineralisation is usually necessary to preserve soft tissue after this time, the presence of polychaete muscle in the nonmineralised Burgess shale shows this need not always be the case.[9] Their preservation potential is similar to that of jellyfish.[9]

Taxonomy and systematics

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See also: List of annelid families
Head of Phyllodoce lineata
The plumes of the feather duster worm are used to filter water
Planktonic bristleworm Tomopteris
Christmas tree worms
Rag worms can be dangerous to touch, giving painful burns
Sandworms eat seaweed and microorganisms and can be longer than four feet
Giant tube worms can tolerate extremely high hydrogen sulfide levels

Taxonomically, polychaetes are thought to be paraphyletic,[28] meaning the group excludes some descendants of its most recent common ancestor. Groups that may be descended from the polychaetes include the clitellates (earthworms and leeches), sipunculans, and echiurans. The Pogonophora and Vestimentifera were once considered separate phyla, but are now classified in the polychaete family Siboglinidae.

Much of the classification below matches Rouse & Fauchald, 1998, although that paper does not apply ranks above family.

Older classifications recognize many more (sub)orders than the layout presented here. As comparatively few polychaete taxa have been subject to cladistic analysis, some groups which are usually considered invalid today may eventually be reinstated.

These divisions were shown to be mostly paraphyletic in recent years.

See also

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References

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Bibliography

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  • Campbell, Reece, and Mitchell. Biology. 1999.
  • Rouse, Greg W.; Fauchald, Kristian (1998). "Recent views on the status, delineation, and classification of the Annelida". American Zoologist. 38 (6): 953–964. doi:10.1093/icb/38.6.953.

Notes

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  1. ^ a b 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.
  2. ^ Geography of Guam Archived 1996-10-27 at the Wayback Machine ns.gov.gu Accessed Oct. 8, 2009
  3. ^ Glasby, Cristopher; Timm, Tarmo (2008). E. V. Balian; C. Lévêque; H. Segers; K. Martens (eds.). "Global diversity of polychaetes (Polychaeta: Annelida) in freshwater". Hydrobiologia. 595 (1: Freshwater Animal Diversity Assessment): 107–115. CiteSeerX 10.1.1.655.4467. doi:10.1007/s10750-007-9008-2. S2CID 13143924.
  4. ^ a b c d e f g Barnes, Robert D. (1982). Invertebrate Zoology. Philadelphia, PA: Holt-Saunders International. pp. 469–525. ISBN 978-0-03-056747-6.
  5. ^ High-resolution vision in pelagic polychaetes
  6. ^ "14 Fun Facts About Marine Bristle Worms".
  7. ^ Kanie, Shusei; Miura, Daisuke; Jimi, Naoto; Hayashi, Taro; Nakamura, Koji; Sakata, Masahiko; Ogoh, Katsunori; Ohmiya, Yoshihiro; Mitani, Yasuo (2021-09-27). "Violet bioluminescent Polycirrus sp. (Annelida: Terebelliformia) discovered in the shallow coastal waters of the Noto Peninsula in Japan". Scientific Reports. 11 (1): 19097. Bibcode:2021NatSR..1119097K. doi:10.1038/s41598-021-98105-6. ISSN 2045-2322. PMC 8476577. PMID 34580316.
  8. ^ Zörner, S. A.; Fischer, A. (22 Dec 2006). "The spatial pattern of bioluminescent flashes in the polychaete Eusyllis blomstrandi (Annelida)". Helgoland Marine Research. 61 (1): 55–66. doi:10.1007/s10152-006-0053-4. ISSN 1438-3888. S2CID 2473677.
  9. ^ a b c d Briggs, Derek E. G.; Kear, Amanda J. (8 February 2016). "Decay and preservation of polychaetes: taphonomic thresholds in soft-bodied organisms". Paleobiology. 19 (1): 107–135. Bibcode:1993Pbio...19..107B. doi:10.1017/S0094837300012343. JSTOR 2400774. S2CID 84073818.
  10. ^ Annelids in Extreme Aquatic Environments: Diversity, Adaptations and Evolution
  11. ^ a b Martin, Daniel; Nygren, Arne; Cruz-Rivera, Edwin (2017-06-01). "Proceraea exoryxae sp. nov. (Annelida, Syllidae, Autolytinae), the first known polychaete miner tunneling into the tunic of an ascidian". PeerJ. 5: e3374. doi:10.7717/peerj.3374. ISSN 2167-8359. PMC 5457667. PMID 28584710.
  12. ^ a b c Martin, Daniel; Britayev, Temir A. (1998). "SYMBIOTIC POLYCHAETES: REVIEW OF KNOWN SPECIES". Oceanography and Marine Biology: An Annual Review. CRC Press. pp. 225–254. doi:10.1201/b12646-22 (inactive 2024-09-12). hdl:10261/39328. ISBN 9780429210600.{{cite book}}: CS1 maint: DOI inactive as of September 2024 (link)
  13. ^ Abe, Hirokazu; Hoshino, Osamu; Yamada, Kazuyuki; Ogino, Tetsuya; Kawaida, Shun; Sato-Okoshi, Waka (2022-06-28). "A novel symbiotic relationship between ascidians and a new tunic-boring polychaete (Annelida: Spionidae: Polydora)". Zootaxa. 5159 (1): 1–22. doi:10.11646/zootaxa.5159.1.1. ISSN 1175-5334. PMID 36095560.
  14. ^ "Bristleworm". MESA.[self-published source]
  15. ^ "'Zombie worms' found off Sweden". BBC News. 18 October 2005. Retrieved 12 February 2010.
  16. ^ Accessed Oct. 8, 2009 Archived 1996-10-27 at the Wayback Machine Geography of the ocean floor near Guam with some notes on exploration of the Challenger Deep.
  17. ^ A tiny worm sheds light into genome compaction
  18. ^ Martín-Durán, José M.; Vellutini, Bruno C.; Marlétaz, Ferdinand; Cetrangolo, Viviana; Cvetesic, Nevena; Thiel, Daniel; Henriet, Simon; Grau-Bové, Xavier; Carrillo-Baltodano, Allan M.; Gu, Wenjia; Kerbl, Alexandra; Marquez, Yamile; Bekkouche, Nicolas; Chourrout, Daniel; Gómez-Skarmeta, Jose Luis; Irimia, Manuel; Lenhard, Boris; Worsaae, Katrine; Hejnol, Andreas (2020). "Conservative route to genome compaction in a miniature annelid". Nature Ecology & Evolution. 5 (2): 231–242. Bibcode:2020NatEE...5..231M. doi:10.1038/s41559-020-01327-6. PMC 7854359. PMID 33199869.
  19. ^ Piper, Ross (2007). Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals. Greenwood Press. ISBN 9780313339226.
  20. ^ Frost, Emily; Waters, Hannah (1 July 2015). "Some polychaetes have sex lives out of a science fiction movie". 14 fun facts about marine bristle worms. Smithsonian.com. Retrieved 9 August 2017.
  21. ^ Conway Morris, S.; Peel, J. S. (2008). "The Earliest Annelids: Lower Cambrian Polychaetes from the Sirius Passet Lagerstätte, Peary Land, North Greenland". Acta Palaeontologica Polonica. 53: 137–148. doi:10.4202/app.2008.0110.
  22. ^ Butterfield, N. J. (1990). "A reassessment of the enigmatic Burgess Shale fossil Wiwaxia corrugata (Matthew) and its relationship to the polychaete Canadia spinosa Walcott". Paleobiology. 16 (3): 287–303. Bibcode:1990Pbio...16..287B. doi:10.1017/S0094837300010009. JSTOR 2400789. S2CID 88100863.
  23. ^ Smith, M. R. (2012). "Mouthparts of the Burgess Shale fossils Odontogriphus and Wiwaxia: Implications for the ancestral molluscan radula". Proceedings of the Royal Society B. 279 (1745): 4287–4295. doi:10.1098/rspb.2012.1577. PMC 3441091. PMID 22915671.
  24. ^ Smith, M. R. (2014). "Ontogeny, morphology and taxonomy of the soft-bodied Cambrian 'mollusc' Wiwaxia". Palaeontology. 57 (1): 215–229. Bibcode:2014Palgy..57..215S. doi:10.1111/pala.12063. S2CID 84616434.
  25. ^ Miller, A. J. (2004). A revised morphology of Cloudina with ecological and phylogenetic implications. CiteSeerX 10.1.1.526.5035.
  26. ^ Vinn, Olev; Zatoń, Michał (March 2012). "Inconsistencies in proposed annelid affinities of early biomineralized organism Cloudina (Ediacaran): structural and ontogenetic evidences". Carnets de Géologie (Lettres). doi:10.4267/2042/46095.
  27. ^ Vinn, O; Mutvei, H (2009). "Calcareous tubeworms of the Phanerozoic". Estonian Journal of Earth Sciences. 58 (4): 286. doi:10.3176/earth.2009.4.07.
  28. ^ Westheide, W. (1997). "The direction of evolution within the Polychaeta". Journal of Natural History. 31 (1): 1–15. Bibcode:1997JNatH..31....1W. doi:10.1080/00222939700770011.
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