Nudibranch

Nudibranchs (/ˈnjuːdɪbræŋk/[2]) are a group of soft-bodied, marine gastropod molluscs which shed their shells after their larval stage.[3] They are noted for their often extraordinary colours and striking forms, and they have been given colourful nicknames to match, such as "clown," "marigold," "splendid," "dancer," "dragon,"[4] or "sea rabbit." [5] Currently, about 3,000 valid species of nudibranchs are known.[6]

Nudibranch
Berghia coerulescens
Chromodoris lochi pair in Puerto Galera, the Philippines
Scientific classification
Kingdom: Animalia
Phylum: Mollusca
Class: Gastropoda
Subclass: Heterobranchia
Clade: Nudipleura
Order: Nudibranchia
Cuvier, 1817
Clades

See text for superfamilies

Diversity[1]
about 3000 species

The word "nudibranch" comes from the Latin nudus "naked" and the Ancient Greek βράγχια (bránkhia) "gills".

Nudibranchs are often casually called sea slugs, as they are a family of opistobranchs (sea slugs), within the phylum Mollusca (molluscs), but many sea slugs belong to several taxonomic groups which are not closely related to nudibranchs. A number of these other sea slugs, such as the photosynthetic Sacoglossa and the colourful Aglajidae, are often confused with nudibranchs.

Distribution and habitat
Janolus sp. in Anilao, the Philippines
Kalinga ornata from Anilao Pier dive site, depth 5 m

Nudibranchs occur in seas worldwide, ranging from the Arctic, through temperate and tropical regions, to the Southern Ocean around Antarctica.[6][7][8] They are almost entirely restricted to salt water, although a few species are known to inhabit lower salinities in brackish water.[9]

Nudibranchs live at virtually all depths, from the intertidal zone to depths well over 700 m (2,300 ft).[7] The greatest diversity of nudibranchs is seen in warm, shallow reefs, although a new nudibranch species was discovered at a depth near 2,500 m (8,200 ft).[10]

Nudibranchs are benthic animals, found crawling over the substrate.[7] The only exceptions to this are the neustonic Glaucus nudibranchs, which float upside down just under the ocean's surface; the pelagic nudibranchs Cephalopyge trematoides, which swim in the water column;[11][12] and Phylliroe bucephalum.[13]

Anatomical description
Berghia stephanieae nudibranch body: Note the oral tentacles (ot), foot tentacles (ft), eye (e), rhinophores (r), and cerata (c). This species has cnidosacs (cn) at the cerata tips. Scale bar is 100 μm.

The body forms of nudibranchs vary a great deal, but because they are opisthobranchs, unlike most other gastropods, they are apparently bilaterally symmetrical externally (but not internally) because they have undergone secondary detorsion. In all nudibranchs, the male and female sexual openings are on the right side of the body, reflecting their asymmetrical origins. They lack a mantle cavity. Some species have venomous appendages (cerata) on their sides, which deter predators. Many also have a simple gut and a mouth with a radula.[14]

The eyes in nudibranchs are simple and able to discern little more than light and dark.[15] The eyes are set into the body, are about a quarter of a millimeter in diameter, and consist of a lens and five photoreceptors.[16]

Nudibranchs vary in adult size from 4 to 600 mm (0.16 to 23.62 in).

The adult form is without a shell or operculum (in shelled gastropods, the operculum is a bony or horny plate that can cover the opening of the shell when the body is withdrawn). In most species is a swimming veliger larva with a coiled shell which is shed at metamorphosis when the larva transforms into the adult form. Some species have direct development, and the shell is shed before the animal emerges from the egg mass.[14]

The name nudibranch is appropriate, since the dorids (infraclass Anthobranchia) breathe through a "naked gill" shaped into branchial plumes in a rosette on their backs.[17] By contrast, on the back of the aeolids in the clade Cladobranchia, brightly coloured sets of protruding organs called cerata are present.

Nudibranchs have cephalic (head) tentacles, which are sensitive to touch, taste, and smell. Club-shaped rhinophores detect odors.

Defence mechanisms
Nudibranchs (Nembrotha kubaryana) eating Clavelina tunicate colonies

In the course of their evolution, nudibranchs have lost their shells, while developing alternative defence mechanisms. Some species evolved an external anatomy with textures and colours that mimicked surrounding sessile invertebrate animals (often their prey sponges or soft corals) to avoid predators (camouflage). Other nudibranchs, as seen especially well on chromodorids, have an intensely bright and contrasting colour pattern that makes them especially conspicuous in their surroundings. Nudibranch molluscs are the most commonly cited examples of aposematism in marine ecosystems, but the evidence for this has been contested,[18] mostly because few examples of mimicry are seen among species, many species are nocturnal or cryptic, and bright colours at the red end of the spectrum are rapidly attenuated as a function of water depth. For example, the Spanish dancer nudibranch (genus Hexabranchus), among the largest of tropical marine slugs, potently chemically defended, and brilliantly red and white, is nocturnal and has no known mimics.[19] Other studies of nudibranch molluscs have concluded they are aposematically coloured, for example, the slugs of the family Phylidiidae from Indo-Pacific coral reefs.[20]

Nudibranchs that feed on hydrozoids can store the hydrozoids' nematocysts (stinging cells) in the dorsal body wall, the cerata.[21] These stolen nematocysts, called kleptocnidae, wander through the alimentary tract without harming the nudibranch. Once further into the organ, the cells are assimilated by intestinal protuberances and brought to specific placements on the creature's hind body. Nudibranchs can protect themselves from the hydrozoids and their nematocysts; the specific mechanism is yet unknown, but special cells with large vacuoles probably play an important role. Similarly, some nudibranchs can also take in plant cells (symbiotic algae from soft corals) and reuse these to make food for themselves. The related group of sacoglossan sea slugs feed on algae and retain just the chloroplasts for their own photosynthetic use, a process known as kleptoplasty.

Nudibranchs use a variety of chemical defences to aid in protection,[22] but it is not necessary for the strategy to be lethal to be effective; in fact, good arguments exist that chemical defences should evolve to be distasteful rather than toxic.[23] Some sponge-eating nudibranchs concentrate the chemical defences from their prey sponge in their bodies, rendering themselves distasteful to predators.[19][24] The evidence that suggests the chemical compounds used by dorid nudibranchs do in fact come from dietary sponges lies in the similarities between the metabolites of prey and nudibranchs, respectively. Furthermore, nudibranchs contain a mixture of sponge chemicals when they are in the presence of multiple food sources, as well as change defence chemicals with a concurrent change in diet.[25] This, however, is not the only way for nudibranchs to develop chemical defences. Certain species are able to produce their own chemicals de novo without dietary influence. Evidence for the different methods of chemical production comes with the characteristic uniformity of chemical composition across drastically different environments and geographic locations found throughout de novo production species compared to the wide variety of dietary and environmentally dependent chemical composition in sequestering species.[26]

Another method of protection is the release of an acid from the skin.[27] Once the specimen is physically irritated or touched by another creature, it will release the mucus automatically.

Apparent production of sound

In 1884, Philip Henry Gosse reported observations by "Professor Grant" (possibly Robert Edmond Grant) that two species of nudibranchs emit sounds that are audible to humans.[28]

Two very elegant species of Sea-slug, viz., Eolis punctata [i.e. Facelina annulicornis], and Tritonia arborescens [i.e. Dendronotus frondosus], certainly produce audible sounds. Professor Grant, who first observed the interesting fact in some specimens of the latter which he was keeping in an aquarium, says of the sounds, that 'they resemble very much the clink of a steel wire on the side of the jar, one stroke only been given at a time, and repeated at intervals of a minute or two; when placed in a large basin of water the sound is much obscured, and is like that of a watch, one stroke being repeated, as before, at intervals. The sound is longest and most often repeated when the Tritonia are lively and moving about, and is not heard when they are cold and without any motion; in the dark I have not observed any light emitted at the time of the stroke; no globule of air escapes to the surface of the water, nor is any ripple produced on the surface at the instant of the stroke; the sound, when in a glass vessel, is mellow and distinct.' The Professor has kept these Tritonia alive in his room for a month, and during the whole period of their confinement they have continued to produce the sounds with very little diminution of their original intensity. In a small apartment they are audible at the distance of twelve feet. The sounds obviously proceed from the mouth of the animal; and at the instant of the stroke, we observe the lips suddenly separate, as if to allow the water to rush into a small vacuum formed within. As these animals are hermaphrodites, requiring mutual impregnation, the sounds may possibly be a means of communication between them, or, if they are of an electric nature, they may be the means of defending from foreign enemies one of the most delicate, defenceless, and beautiful Gasteropods that inhabit the deep.

Lifecycle
Mating behavior in Nembrotha purpureolineata
Acanthodoris lutea laying eggs

Nudibranchs are hermaphroditic, thus have a set of reproductive organs for both sexes, but they cannot fertilize themselves.[29] Mating usually takes a few minutes, and involves a dance-like courtship. Nudibranchs typically deposit their eggs within a gelatinous spiral,[30] which is often described as looking like a ribbon. The number of eggs varies; it can be as few as just 1 or 2 eggs (Vayssierea felis) or as many as an estimated 25 million (Aplysia fasciata). The eggs contain toxins from sea sponges as a means of deterring predators.[31] After hatching, the infants look almost identical to their adult counterparts, albeit smaller. Infants may also have fewer cerata. The lifespan of nudibranchs can range from a few weeks to a year, depending on the species.

Feeding and ecological role
Pteraeolidia ianthina has adapted cerata to house symbiotic zooxanthellae obtained from its diet, which continue to photosynthesize and provide energy to the nudibranch.

All known nudibranchs are carnivorous.[29] Some feed on sponges, others on hydroids (e.g. Cuthona),[32] others on bryozoans (phanerobranchs such as Tambja, Limacia, Plocamopherus and Triopha),[33] and some eat other sea slugs or their eggs (e.g. Favorinus)[34] or, on some occasions, are cannibals and prey on members of their own species. Other groups feed on tunicates (e.g. Nembrotha, Goniodoris),[35] other nudibranchs (Roboastra, which are descended from tunicate-feeding species),[35] barnacles (e.g. Onchidoris bilamellata),[36] and anemones (e.g. the Aeolidiidae and other Cladobranchia).[33]

The surface-dwelling nudibranch, Glaucus atlanticus, is a specialist predator of siphonophores, such as the Portuguese man o' war. This predatory mollusc sucks air into its stomach to keep it afloat, and using its muscular foot, it clings to the surface film. If it finds a small victim, Glaucus simply envelops it with its capacious mouth, but if the prey is a larger siphonophore, the mollusc nibbles off its fishing tentacles, the ones carrying the most potent nematocysts. Like some others of its kind, Glaucus does not digest the nematocysts; instead, it uses them to defend itself by passing them from its gut to the surface of its skin.[37]

Taxonomy
Dorids (Chromodoris willani shown) breathe with the branchial plume, which projects from around their anus.
Aeolids (Hermissenda crassicornis pictured) have many cerata over their back which are used for defense and respiration.
Nudibranchs are frequently differentiated as either dorid or aeolid.

Nudibranchs are commonly divided into two main kinds, dorid and aeolid (also spelled eolid) nudibranchs:[38][39]

  • Dorids (clade Anthobranchia, Doridacea, or Doridoidea) are recognised by the branchial (gill) plume, which forms a cluster on the posterior part of the body, around the anus. Fringes on the mantle do not contain any intestines.
  • Aeolids (clade Cladobranchia) have cerata (spread across the back) instead of the branchial plume. They lack a mantle. Some are hosts to zooxanthellae.

The exact systematics of nudibranchs are a topic of recent revision. Traditionally, nudibranchs have been treated as the order Nudibranchia, located in the gastropod mollusc subclass Opisthobranchia (the marine slugs: which consisted of nudibranchs, sidegill slugs, bubble snails, algae sap-sucking sea slugs, and sea hares).[38] Since 2005,[40] pleurobranchs (which had previously been grouped among sidegill slugs) have been placed alongside nudibranchs in the clade Nudipleura (recognising them as more closely related to each other than to other opisthobranchs).[41] Since 2010, Opisthobranchia has been recognised as not a valid clade (it is paraphyletic) and instead Nudipleura has been placed as the first offshoot of Euthyneura (which is the dominant clade of gastropods).[42]


Traditional hierarchy

This classification was based on the work of Johannes Thiele (1931),[43] who built on the concepts of Henri Milne-Edwards (1848).[44]

Order Nudibranchia:

Early revisions

Newer insights derived from morphological data and gene-sequence research seemed to confirm those ideas. On the basis of investigation of 18S rDNA sequence data, strong evidence supports the monophyly of the Nudibranchia and its two major groups, the Anthobranchia/Doridoidea and Cladobranchia.[45] A study published in May 2001, again revised the taxonomy of the Nudibranchia.[46] They were thus divided into two major clades:

However, according to the taxonomy by Bouchet & Rocroi (2005), currently the most up-to-date system of classifying the gastropods, the Nudibranchia are a subclade within the clade of the Nudipleura. The Nudibranchia are then divided into two clades:

This gallery shows some of the great variability in the color and form of nudibranchs, and nudibranch egg ribbons.

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gollark: Birch Forest, why?

See also

References
  1. Wägele, H.; Klussmann-Kolb, A. (2005). "Opisthobranchia (Mollusca, Gastropoda) more than just slimy slugs. Shell reduction and its implications on defence and foraging". Frontiers in Zoology. 2: 1–18. doi:10.1186/1742-9994-2-3. PMC 554092. PMID 15715915.
  2. Longman Pronunciation Dictionary (2nd edition), ISBN 0-582-36467-1
  3. Thompson, T. E. (2009). "Feeding in nudibranch larvae" (PDF). Journal of the Marine Biological Association of the United Kingdom. 38 (2): 239–248. doi:10.1017/S0025315400006044.
  4. Turnbull, John (Spring 2016). "The Nudibranch - Creature Feature". Nature New South Wales. 60 (3): 16–17.
  5. Bronson, Wilfrid. Water People, 1935
  6. Ocean Portal (2017). A Collage of Nudibranch Colors. Smithsonian National Museum of Natural History. Retrieved 17 April 2018.
  7. Nudibranchs, Fishermen Scuba.
  8. Ekimova, I.; T. Korshunova; D. Schepetov; T. Neretina; N. Sanamyan; A. Martynov (2015). "Integrative systematics of northern and Arctic nudibranchs of the genus Dendronotus (Mollusca, Gastropoda), with descriptions of three new species". Zoological Journal of the Linnean Society. 173 (4): e0192177. doi:10.1111/zoj.12214.
  9. Korshunova, T.; K. Lundin; K. Malmberg; B. Picton; A. Martynov (2018). "First true brackish-water nudibranch mollusc provides new insights for phylogeny and biogeography and reveals paedomorphosis-driven evolution". PLoS ONE. 13 (1): e0192177. doi:10.1371/journal.pone.0192177. PMC 5851531. PMID 29538398.
  10. "Discoveries of deep-sea biomass and biodiversity using an ROV". Monterey Bay Aquarium Research Institute. Archived from the original on 9 October 2013. Retrieved 16 October 2013.
  11. Steinberg, J. E. (1956). "The pelagic nudibranch, Cephalopyge trematoides (Chun, 1889), in New South Wales with a note on other species in this genus". Proceedings of the Linnean Society of New South Wales. 81: 184–192.
  12. G.M. Mapstone & M.N. Arai, Siphonophora (Cnidaria, Hydrozoa) of Canadian Pacific Waters, p.33. "The best documented predators of pelagic cnidarians from the phylum Mollusca are the neustonic nudibranchs and snails [...and] the pelagic nudibranch [...]"
  13. Gosliner TM, Valdes A Behrens DW 2015 Nudibranch and Sea Slug Identification Indo-Pacific New World Publications Jacksonville Florida USA
  14. Thompson, T. E. 1976. Biology of opisthobranch molluscs, vol. 1, 207 pp., 21 pls. Ray Society, no. 151.
  15. "Nudibranchs – National Geographic Magazine". Ngm.nationalgeographic.com. 2013-04-25. Retrieved 2013-07-04.
  16. CHASE, RONALD (June 1, 1974). "The Electrophysiology of Photoreceptors in the Nudibranch Mollusc, Tritonia Diomedia". Journal of Experimental Biology. 60 (3): 707–19. PMID 4847278.
  17. Dayrat, B. (2005). "Advantages of naming species under the PhyloCode: An example of how a new species of Discodorididae (Mollusca, Gastropoda, Euthyneura, Nudibranchia, Doridina) may be named" (PDF). Marine Biology Research. 1 (3): 216–232. doi:10.1080/17451000510019141. Retrieved 2009-06-14.
  18. Edmunds, M. (1991). "Does warning colouration occur in nudibranchs?". Malacologia. 32: 241–255.
  19. Pawlik, JR; et al. (1988). "Defensive chemicals of the Spanish Dancer nudibranch, Hexabranchus sanguineus, and its egg ribbons: Macrolides derived from a sponge diet". Journal of Experimental Marine Biology and Ecology. 119 (2): 99–109. doi:10.1016/0022-0981(88)90225-0.
  20. Ritson-Williams, R.; Paul, VJ (2007). "Marine benthic invertebrates use multimodal cues for defence against reef fish". Marine Ecology Progress Series. 340: 29–39. doi:10.3354/meps340029.
  21. Frick, K (2003). "Predator Suites and Flabellinid Nudibranch Nematocyst Complements in the Gulf of Maine". In: SF Norton (Ed). Diving for Science...2003. Proceedings of the American Academy of Underwater Sciences (22nd Annual Scientific Diving Symposium). Retrieved 2008-07-03.
  22. Karuso, P. (1987). "Chemical Ecology of the Nudibranchs". In Scheuer, PJ (ed.). Bioorganic Marine Chemistry. 1. Springer-Verlag. pp. 31–60. doi:10.1007/978-3-642-72726-9_2. ISBN 978-3-642-72728-3., a comprehensive review of the chemical ecology of the nudibranchs
  23. Pawlik, JR (2012). Fattorusso, E.; et al. (eds.). Antipredatory defensive roles of natural products from marine invertebrates. Handbook of Marine Natural Products. NY: Springer Science. pp. 677–710.
  24. Gosliner, T. M. (1987). Nudibranchs of Southern Africa. ISBN 978-0-930118-13-6.
  25. Faulkner, D. J.; Ghiselin, M. T. (1983). "Chemical defence and evolutionary ecology of dorid nudibranchs and some other opisthobranch gastropods". Marine Ecology Progress Series. 13: 295–301. doi:10.3354/meps013295.
  26. Barsby, T.; Linington, R. G.; Andersen, R. J. (2002). "De Novo terpenoid biosynthesis by the dendronotid nudibranch Melibe leonina". Chemoecology. 12 (4): 199–202. doi:10.1007/PL00012669.
  27. Edmunds, M. (1968). "Acid secretion in some species of Doridacea (Mollusca, Nudibranchia)". Proceedings of the Malacological Society of London. 38 (2): 121–133.
  28. P.H. Gosse, Evenings at the Microscope, 1884 edition, p57
  29. "Nudibranch". Aquaticcommunity.com. Retrieved 2013-07-04.
  30. Klussmann-Kolb A (2001). "The Reproductive Systems of the Nudibranchia (Gastropoda, Opisthobranchia): Comparative Histology and Ultrastructure of the Nidamental Glands with Aspects of Functional Morphology". Zoologischer Anzeiger. 240 (2): 119–136. doi:10.1078/0044-5231-00011.
  31. "Diving with Nudibranchs". Dive the World.
  32. NC Folino (1997). "The role of prey mobility in the population ecology of the nudibranch Cuthona nana (Gastropoda: Opisthobranchia)" (PDF). American Malacological Bulletin. Archived from the original (PDF) on 2012-06-25. Retrieved 2013-03-07.
  33. Domínguez, M.; Troncoso, J. S.; García, F. J. (2008). "The family Aeolidiidae Gray, 1827 (Gastropoda Opisthobranchia) from Brazil, with a description of a new species belonging to the genus Berghia Trinchese, 1877". Zoological Journal of the Linnean Society. 153 (2): 349–368. doi:10.1111/j.1096-3642.2008.00390.x.
  34. Rudman, W.B. (1999-03-19). "Favorinus tsuruganus Baba & Abe, 1964. [In] Sea Slug Forum. Australian Museum".
  35. Valdés, Á. (2004). "Phylogeography and phyloecology of dorid nudibranchs (Mollusca, Gastropoda)". Biological Journal of the Linnean Society. 83 (4): 551–559. doi:10.1111/j.1095-8312.2004.00413.x.
  36. Barnes, H.; Powell, H. T. (1954). "Onchidoris fusca (Müller); A Predator of Barnacles". Journal of Animal Ecology. 23 (2): 361–363. doi:10.2307/1986. JSTOR 1986.
  37. Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
  38. Hans Bertsch, Nudibranchs: Marine slugs with verve. "Navanax inermis[..] is the bane of all nudibranchs, because it is one of the few known predators on this group of slugs. [...] Dorids mainly eat sponges, bryozoans, and tunicates, whereas aeolids principally eat cnidarians."
  39. "Facts About Nudibranchs". Marinelife.about.com. 2011-11-10. Retrieved 2013-07-04.
  40. Taxonomy of the Gastropoda, Bouchet & Rocroi, 2005
  41. Guido T. Poppe & Sheila P. Tagaro, The New Classification of Gastropods according to Bouchet & Rocroi, 2005; Visaya, February 23, 2006 Archived September 27, 2007, at the Wayback Machine
  42. Jörger, K. M.; Stöger, I.; Kano, Y.; Fukuda, H.; Knebelsberger, T.; Schrödl, M. (2010). "On the origin of Acochlidia and other enigmatic euthyneuran gastropods, with implications for the systematics of Heterobranchia". BMC Evolutionary Biology. 10: 323. doi:10.1186/1471-2148-10-323. PMC 3087543. PMID 20973994. At the basis of the Euthyneura the Nudipleura split off
  43. Thiele, J. (1931). Handbuch der systematischen Weichtierkunde, II. Verlag von Gustav Fischer, Jena, Germany.
  44. Milne-Edwards H (1848). Note sur la classification naturelle chez Mollusques Gasteropodes. Annales des Sciences Naturelles, series 3, 9: 102-112.
  45. Wägele H. & Willan R. C. (September 2000). "Phylogeny of the Nudibranchia". Zoological Journal of the Linnean Society. 130 (1): 83–181. doi:10.1111/j.1096-3642.2000.tb02196.x.
  46. Schrödl M., Wägele H. & Willan R. C. (2001). "Taxonomic Redescription of the Doridoxidae(Gastropoda: Opisthobranchia), an Enigmatic Family of Deep Water Nudibranchs, with Discussion of Basal Nudibranch Phylogeny". Zoologischer Anzeiger. 240 (1): 83–97. doi:10.1078/0044-5231-00008.

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