|Chromodoris lochi pair in Puerto Galera, the Philippines.|
|about 3000 species|
Nudibranchs (//) are a group of soft-bodied, marine gastropod molluscs which shed their shells after their larval stage. 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" and "Dragon". Currently, about 2,300 valid species of nudibranchs are known.
Nudibranchs are often casually called sea slugs, as they are a family of Opistobranchs (sea slugs), with 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
Nudibranchs live at virtually all depths of salt water, from the intertidal zone to depths well over 700 m (2,300 ft). 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).
Nudibranchs are benthic animals, found crawling over the substrate. The only exceptions to this are the neustonic Glaucus nudibranchs, which float upside down just under the ocean's surface, and the pelagic nudibranchs Cephalopyge trematoides, which swims in the water column and Phylliroe bucephalum.
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.
The eyes in nudibranchs are simple and able to discern little more than light and dark. The eyes are set into the body, are about a quarter of a millimeter in diameter, and consist of a lens and five photoreceptors.
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(in shelled gastropods, the operculum is a bony or horny plate that can cover the opening of the shell when the body is withdrawn).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.
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. By contrast, on the back of the aeolids in the clade Cladobranchia there are brightly coloured sets of protruding organs called cerata.
Nudibranchs have cephalic (head) tentacles, which are sensitive to touch, taste, and smell. Club-shaped rhinophores detect odors.
This group includes some of the most colourful creatures on earth. In the course of their evolution, nudibranchs have lost their shell while developing alternative defense mechanisms. Some species evolved an external anatomy with textures and colors that mimicked surrounding sessile invertebrate animals (often their prey sponges or soft corals) to avoid predators (see camouflage). Other nudibranchs, as seen especially well on chromodorids, have an intensely bright and contrasting color 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, mostly because few examples of mimicry are seen among species, many species are nocturnal or cryptic, and bright colors 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. Other studies of nudibranch molluscs have concluded they are aposematically colored, for example, the slugs of the family Phylidiidae from Indo-Pacific coral reefs.
Nudibranchs that feed on hydrozoids can store the hydrozoids' nematocysts (stinging cells) in the dorsal body wall, the cerata. 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 defenses to aid in protection, but it is not necessary for the strategy to be lethal to be effective; in fact, good arguments exist that chemical defenses should evolve to be distasteful rather than toxic. Some sponge-eating nudibranchs concentrate the chemical defences from their prey sponge in their bodies, rendering themselves distasteful to predators. 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 defense chemicals with a concurrent change in diet. This, however, is not the only way for nudibranchs to develop chemical defenses. 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.
Another method of protection is the release of an acid from the skin. Once the specimen is physically irritated or touched by another creature, it will release the mucus automatically.
Apparent production of sound
"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."
Nudibranchs are hermaphroditic, thus have a set of reproductive organs for both sexes, but they cannot fertilize themselves. Nudibranchs typically deposit their eggs within a gelatinous spiral.
Feeding and ecological role
All known nudibranchs are carnivorous. Some feed on sponges, others on hydroids,(e.g. Cuthona) others on bryozoans (phanerobranchs such as Tambja, Limacia, Plocamopherus and Triopha), and some eat other sea slugs or their eggs (e.g. Favorinus) or, on some occasions, are cannibals and prey on members of their own species. Other groups feed on tunicates (e.g. Nembrotha, Goniodoris), other nudibranchs (Roboastra, which are descended from tunicate-feeding species), barnacles (e.g. Onchidoris bilamellata), and anemones (e.g. the Aeolidiidae and other Cladobranchia).
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.
- 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). Since 2005, 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). 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).
- Infraorder Anthobranchia Férussac, 1819 (dorids)
- Infraorder Cladobranchia Willan & Morton, 1984 (aeolids)
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. A study published in May 2001, again revised the taxonomy of the Nudibranchia. They were thus divided into two major clades:
- Anthobranchia (= Bathydoridoidea + Doridoidea)
- Dexiarchia nom. nov. (= Doridoxoidea + Dendronotoidea + Aeolidoidea + "Arminoidea").
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:
- Euctenidiacea (= Holohepatica)
- Dexiarchia (= Actenidiacea)
This gallery shows some of the great variability in the color and form of nudibranchs, and nudibranch egg ribbons.
Nembrotha chamberlaini from Verde Island, the Philippines
Chromodoris dianae from Verde Island, the Philippines
A pair of Nembrotha milleri mating at Verde Island, the Philippines
Regal sea goddess Felimare picta in the Gray's Reef National Marine Sanctuary, Savannah, Georgia
- 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.
- Longman Pronunciation Dictionary (2nd edition), ISBN 0-582-36467-1
- Thompson, T. E. (2009). "Feeding in nudibranch larvae". Journal of the Marine Biological Association of the United Kingdom. 38 (2): 239. doi:10.1017/S0025315400006044.
- Turnbull, John (Spring 2016). "The Nudibranch - Creature Feature". Nature - New South Wales (Journal of National Parks Association of NSW). 60 (3): 16–17.
- Gofas, S. (2014). Nudibranchia. Accessed through: World Register of Marine Species at http://www.marinespecies.org/aphia.php?p=taxdetails&id=1762 on 2015-02-12
- Nudibranchs, Fishermen Scuba.
- "Discoveries of deep-sea biomass and biodiversity using an ROV". Monterey Bay Aquarium Research Institute. Retrieved 16 October 2013.
- 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.
- 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 [...]"
- Gosliner TM, Valdes A Behrens DW 2015 Nudibranch and Sea Slug Identification Indo-Pacific New World Publications Jacksonville Florida USA
- Thompson, T. E. 1976. Biology of opisthobranch molluscs, vol. 1, 207 pp., 21 pls. Ray Society, no. 151.
- "Nudibranchs – National Geographic Magazine". Ngm.nationalgeographic.com. 2013-04-25. Retrieved 2013-07-04.
- 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.
- 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.
- Edmunds, M. (1991). "Does warning coloration occur in nudibranchs?". Malacologia. 32: 241–255.
- 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: 99–109. doi:10.1016/0022-0981(88)90225-0.
- Ritson-Williams, R.; Paul, VJ (2007). "Marine benthic invertebrates use multimodal cues for defense against reef fish". Marine Ecology Progress Series. 340: 29–39. doi:10.3354/meps340029.
- 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.
- Karuso, P. (1987). Scheuer, PJ, ed. Bioorganic Marine Chemistry. Chemical Ecology of the Nudibranchs. Springer-Verlag. pp. 31–60. ISBN 978-3-642-72728-3., a comprehensive review of the chemical ecology of the nudibranchs
- 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.
- Gosliner, T. M. (1987). Nudibranchs of Southern Africa. ISBN 0-930118-13-8.
- Faulkner, D. J.; Ghiselin, M. T. (1983). "Chemical defense and evolutionary ecology of dorid nudibranchs and some other opisthobranch gastropods" (PDF). Marine Ecology-Progress Series. 13: 295–301. doi:10.3354/meps013295.
- 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.
- Edmunds, M. (1968). "Acid secretion in some species of Doridacea (Mollusca, Nudibranchia)". Proceedings of the Malacological Society of London. 38 (2): 121–133.
- P.H. Gosse, Evenings at the Microscope, 1884 edition, p57
- "Nudibranch". Aquaticcommunity.com. Retrieved 2013-07-04.
- 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.
- NC Folino (1997). "The role of prey mobility in the population ecology of the nudibranch Cuthona nana (Gastropoda: Opisthobranchia)" (PDF). American Malacological Bulletin.
- 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.
- Rudman, W.B., (1999-03-19). "Favorinus tsuruganus Baba & Abe, 1964. [In] Sea Slug Forum. Australian Museum".
- 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.
- Barnes, H.; Powell, H. T. (1954). "Onchidoris fusca (Müller); A Predator of Barnacles". Journal of Animal Ecology. 23 (2): 361–363. JSTOR 1986. doi:10.2307/1986.
- Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
- 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."
- "Facts About Nudibranchs". Marinelife.about.com. 2011-11-10. Retrieved 2013-07-04.
- Taxonomy of the Gastropoda, Bouchet & Rocroi, 2005
- Guido T. Poppe & Sheila P. Tagaro, The New Classification of Gastropods according to Bouchet & Rocroi, 2005; Visaya, February 23, 2006
- 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. PMC . PMID 20973994. doi:10.1186/1471-2148-10-323.
At the basis of the Euthyneura the Nudipleura split off
- Thiele, J. (1931). Handbuch der systematischen Weichtierkunde, II. Verlag von Gustav Fischer, Jena, Germany.
- Milne-Edwards H (1848). Note sur la classification naturelle chez Mollusques Gasteropodes. Annales des Sciences Naturelles, series 3, 9: 102-112.
- Wägele H. & Willan R. C. (September 2000). "Phylogeny of the Nudibranchia". Zoological Journal of the Linnean Society. 1 (1): 83–181. doi:10.1111/j.1096-3642.2000.tb02196.x.
- 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.
- Thompson, T. E. (1976). Biology of opisthobranch molluscs Vol. 1. 207 pp., 21 pls. Ray Society, no. 151.
- Thompson, T. E., & G. H. Brown (1984). Biology of opisthobranch molluscs Vol. 2. 229 pp., 41 pls. Ray Society, no. 156.
- McDonald, Gary R. (September 17, 2009). Institute of Marine Sciences. Bibliographia Nudibranchia, 2nd Edition. A listing, by Author, of publications on nudibranchs.
- McDonald, Gary R. (September 17, 2009). Institute of Marine Sciences. Nudibranch Systematic Index, 2nd Edition. An index of names given to nudibranchs and their subsequent use, referenced to Bibliographia Nudibranchia.
- McDonald, Gary R. & J. W. Nybakken. (November 5, 2014). List of the Worldwide Food Habits of Nudibranchs
- Coleman, Neville (2008). Nudibranchs Encyclopedia: Catalogue of Asia/Indo-Pacific Sea Slugs. Neville Coleman's Underwater Geographic. ISBN 0-947325-41-7
|Wikispecies has information related to: Nudibranchia|
|Wikimedia Commons has media related to Nudibranchia.|
- Sea Slug Forum by William B. Rudman
- Nudibranchs of the British Isles
- OPK Opistobranquis – Iberian and Mediterranean Opisthobranchs
- Mediterranean slug site (actually a misnomer – Worldwide coverage
- The Slug Site, Michael D. Miller 2002–2014
- The Okinawa Slug Site
- Images, information and identification of Nudibranchs
- Nudibranch Photos by Mick Tait
- World of Water by Neville Coleman (Encyclopedia and photos)
- Nudibranchs in their natural environment, Scuba Diving – Narooma NSW offline? 26 Nov 2014
- Nudi Pixel: Online resource for nudibranchs and sea slugs identification using photographs
- Various nudibranch species from Indonesia, Philippines and Thailand
- Nudibranch gallery- Sergey Parinov – offline? 26 Nov 2014
- Opisthobranch Newsletter – Bibliography and portal to opisthobranch, nudibranch & seaslug information
- Scottish Nudibranchs: Online resource for identification of species found in Scottish waters
- National Geographic Nudibranch Photo Gallery
- Sea slugs of Hawaii
- Slug City – Molluscs. Brain & Behavior, from the University of Illinois at Urbana-Champaign