词条 | Amphiprioninae | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
释义 |
| image = Clown fish in the Andaman Coral Reef.jpg | image_caption = Ocellaris clownfish, Amphiprion ocellaris | taxon = Amphiprioninae | display_parents = 3 | authority = Allen, 1975 | subdivision_ranks = Genera | subdivision = Amphiprion Bloch & Schneider, 1801 Premnas Cuvier, 1816 }} Clownfish or anemonefish are fishes from the subfamily Amphiprioninae in the family Pomacentridae. Thirty species are recognized: one in the genus Premnas, while the remaining are in the genus Amphiprion. In the wild, they all form symbiotic mutualisms with sea anemones. Depending on species, anemonefish are overall yellow, orange, or a reddish or blackish color, and many show white bars or patches. The largest can reach a length of {{convert|15-16|cm|in|abbr=on}}, while the smallest barely achieve {{convert|7-8|cm|in|abbr=on}}. Distribution and habitatsAnemonefish are native to the warmer waters of the Indian and Pacific Oceans, including the Great Barrier Reef and the Red Sea. While most species have restricted distributions, others are widespread. Anemonefish live at the bottom of shallow seas in sheltered reefs or in shallow lagoons. No anemonefish are found in the Atlantic.[1] DietAnemonefish are omnivorous and can feed on undigested food from their host anemones, and the fecal matter from the anemonefish provides nutrients to the sea anemone. Anemonefish primarily feed on small zooplankton from the water column, such as copepods and tunicate larvae, with a small portion of their diet coming from algae, with the exception of Amphiprion perideraion, which primarily feeds on algae.{{r|FieldGuide}}[2] They may also consume the tentacles of their host anemone.[3] Symbiosis and mutualismAnemonefish and sea anemones have a symbiotic, mutualistic relationship, each providing a number of benefits to the other. The individual species are generally highly host specific, and especially the genera Heteractis and Stichodactyla, and the species Entacmaea quadricolor are frequent anemonefish partners. The sea anemone protects the anemonefish from predators, as well as providing food through the scraps left from the anemone's meals and occasional dead anemone tentacles, and functions as a safe nest site. In return, the anemonefish defends the anemone from its predators and parasites.[4][5] The anemone also picks up nutrients from the anemonefish's excrement.[6] The nitrogen excreted from anemonefish increases the amount of algae incorporated into the tissue of their hosts, which aids the anemone in tissue growth and regeneration.[2] The activity of the anemonefish results in greater water circulation around the sea anemone,[7] and it has been suggested that their bright coloring might lure small fish to the anemone, which then catches them.[8] Studies on anemonefish have found that they alter the flow of water around sea anemone tentacles by certain behaviours and movements such as "wedging" and "switching". Aeration of the host anemone tentacles allows for benefits to the metabolism of both partners, mainly by increasing anemone body size and both anemonefish and anemone respiration.[9] Several theories are given about how they can survive the sea anemone poison:
Anemonefish are the best known example of fish that are able to live among the venomous sea anemone tentacles, but several others occur, including juvenile threespot dascyllus, certain cardinalfish (such as Banggai cardinalfish), incognito (or anemone) goby, and juvenile painted greenling.[11][12][13] ReproductionIn a group of anemonefish, a strict dominance hierarchy exists. The largest and most aggressive female is found at the top. Only two anemonefish, a male and a female, in a group reproduce – through external fertilization. Anemonefish are sequential hermaphrodites, meaning they develop into males first, and when they mature, they become females. If the female anemonefish is removed from the group, such as by death, one of the largest and most dominant males becomes a female. The remaining males move up a rank in the hierarchy. Anemonefish lay eggs on any flat surface close to their host anemones. In the wild, anemonefish spawn around the time of the full moon. Depending on the species, they can lay hundreds or thousands of eggs. The male parent guards the eggs until they hatch about 6–10 days later, typically two hours after dusk.[14] Parental investmentMost anemonefish are protandrous hermaphrodites, meaning they alternate between the male and female sexes at some point in their lives. Anemonefish colonies usually consist of the reproductive male and female and a few juveniles, which help tend the colony.[15] Although multiple males cohabit an environment with a single female, polygamy does not occur and only the adult pair exhibits reproductive behavior. However, if the largest female dies, the social hierarchy shifts with the breeding male exhibiting protandrous sex reversal to become the breeding female. The largest juvenile then becomes the new breeding male after a period of rapid growth.[16] The existence of protandry in anemonefish may rest on the case that nonbreeders modulate their phenotype in a way that causes breeders to tolerate them. This strategy prevents conflict by reducing competition between the males for one female. For example, by purposefully modifying their growth rate to remain small and submissive, the juveniles in a colony present no threat to the fitness of the adult male, thereby protecting themselves from being evicted by the dominant fish.[17] The reproductive cycle of anemonefish is often correlated with the lunar cycle. Rates of spawning for anemonefish peak around the first and third quarters of the moon. The timing of this spawn means that the eggs hatch around the full moon or new moon periods. One explanation for this lunar clock is that spring tides produce the highest tides during full or new moons. Nocturnal hatching during high tide may reduce predation by allowing for a greater capacity for escape. Namely, the stronger currents and greater water volume during high tide protects the hatchlings by effectively sweeping them to safety. Before spawning, anemonefish exhibit increased rates of anemone and substrate biting, which help prepare and clean the nest for the spawn.[16] In terms of parental care, male anemonefish are often the caretakers of eggs. Before making the clutch, the parents often clear an oval-shaped clutch varying in diameter for the spawn. Fecundity, or reproductive rate, of the females usually ranges from 600 to 1500 eggs depending on her size. In contrast to most animal species, the female only occasionally takes responsibility for the eggs, with males expending most of the time and effort. Male anemonefish care for their eggs by fanning and guarding them for 6 to 10 days until they hatch. In general, eggs develop more rapidly in a clutch when males fan properly, and fanning represents a crucial mechanism of successfully developing eggs. This suggests that males have the ability to control the success of hatching an egg clutch by investing different amounts of time and energy towards the eggs. For example, a male could choose to fan less in times of scarcity or fan more in times of abundance. Furthermore, males display increased alertness when guarding more valuable broods, or eggs in which paternity was guaranteed. Females, though, display generally less preference for parental behavior than males. All these suggest that males have increased parental investment towards the eggs compared to females.[18] TaxonomyHistorically, anemonefish have been identified by morphological features and color pattern in the field, while in a laboratory, other features such as scalation of the head, tooth shape, and body proportions are used.{{r|FieldGuide}} These features have been used to group species into six complexes, clownfish, tomato, skunk, clarkii, saddleback, and maroon.{{r|Goemans}} As can be seen from the gallery, each of the fish in these complexes has a similar appearance. Genetic analysis has shown that these complexes are not monophyletic groups, particularly the 11 species in the A. clarkii group, where only A. clarkii and A. tricintus are in the same clade, with six species,A. allardi A. bicinctus, A. chagosensis, A. chrosgaster, A. fuscocaudatus, A. latifasciatus, and A. omanensis being in an Indian clade, A. chrysopterus having monospecific lineage, and A. akindynos in the Australian clade with A. mccullochi.{{r|Hybrid}} Other significant differences are that A. latezonatus also has monospecific lineage, and A. nigripes is in the Indian clade rather than with A. akallopisos, the skunk anemonefish.{{r|DeAngelis}} A. latezonatus is more closely related to A. percula and Premnas biaculeatus than to the saddleback fish with which it was previously grouped.{{r|Radiation}}{{r|DeAngelis}} Obligate mutualism was thought to be the key innovation that allowed anemonefish to radiate rapidly, with rapid and convergent morhological changes correlated with the ecological niches offered by the host anemones.{{r|Radiation}} The complexity of mitochondrial DNA structure shown by genetic analysis of the Australian clade suggested evolutionary connectivity among samples of A. akindynos and A. mccullochi that the authors theorize was the result of historical hybridization and introgression in the evolutionary past. The two evolutionary groups had individuals of both species detected, thus the species lacked reciprocal monophyly. No shared haplotypes were found between species.{{r|Ecology}} Phylogenetic relationships
Morphological diversity by complexIn the aquariumAnemonefish make up 43% of the global marine ornamental trade, and 25% of the global trade comes from fish bred in captivity, while the majority is captured from the wild,[21][22] accounting for decreased densities in exploited areas.[23] Public aquaria and captive-breeding programs are essential to sustain their trade as marine ornamentals, and has recently become economically feasible.[24][25] It is one of a handful of marine ornamentals whose complete lifecycle has been in closed captivity. Members of some anemonefish species, such as the maroon clownfish, become aggressive in captivity; others, like the false percula clownfish, can be kept successfully with other individuals of the same species.[26] When a sea anemone is not available in an aquarium, the anemonefish may settle in some varieties of soft corals, or large polyp stony corals.[27] Once an anemone or coral has been adopted, the anemonefish will defend it. Anemonefish, however, are not obligately tied to hosts, and can survive alone in captivity.[28][29] In popular cultureIn Disney/Pixar's 2003 film Finding Nemo and its 2016 sequel Finding Dory main characters Marlin and Nemo are clownfish, probably the species A. ocellaris.[30] The popularity of anemonefish for aquaria increased following the release of this the first film associated with an increase in the numbers of those captured in the wild.[31] Notes1. ^{{cite web|url=http://animals.nationalgeographic.com/animals/fish/clown-anemonefish/#|title=Clown Anemonefish, Clown Anemonefish Pictures, Clown Anemonefish Facts – National Geographic|first=National Geographic|last=Society|publisher=}} 2. ^1 {{cite journal|last=Porat|first=D.|author2=Chadwick-Furman, N.E.|title=Effects of anemonefish on giant sea anemones: Ammonium uptake, zooxanthella content and tissue regeneration|journal=Marine and Freshwater Behaviour and Physiology|year=2005|volume=29|issue=1|pages=43–51|doi=10.1080/10236240500057929|url=http://auburn.edu/academic/cosam/faculty/biology/chadwick/website/Publications_files/Porat%20and%20Chadwick%202005.pdf|accessdate=18 April 2013|archive-url=https://web.archive.org/web/20160511011105/http://auburn.edu/academic/cosam/faculty/biology/chadwick/website/Publications_files/Porat%20and%20Chadwick%202005.pdf|archive-date=2016-05-11|dead-url=yes|df=}} 3. ^{{cite journal|last=Fautin|first=D.G.|author2=Guo, C.|author3=Hwang, J.S.|title=Costs and benefits of the symbiosis between the anemoneshrimp Periclimenes brevicarpalis and its host Entacmaea quadricolor.|journal=Marine Ecology Progress Series|year=1995|volume=129|pages=77–84|doi=10.3354/meps129077|bibcode=1995MEPS..129...77F}} 4. ^{{cite web|url=http://animals.nationalgeographic.com/animals/fish/clown-anemonefish/|title=Clown Anemonefish|publisher=National Geographic Society|work= Nat Geo Wild : Animals|accessdate=2011-12-19}} 5. ^{{EOL|212597}} 6. ^Holbrook, S. J. and Schmitt, R. J. Growth, reproduction and survival of a tropical sea anemone (Actiniaria): benefits of hosting anemonefish, 2005, cited in blogspot.com 7. ^{{cite journal|last=Szczebak|first=Joseph T.|author2=Raymond P. Henry |author3=Fuad A. Al-Horani |author4=Nanette E. Chadwick |title=Anemonefish oxygenate their anemone hosts at night|journal=Journal of Experimental Biology|year=2013|volume=216|issue=9|pages=970–976|doi=10.1242/jeb.075648 |pmid=23447664}} 8. ^{{cite web|url=http://marinebio.org/species.asp?id=29|title=Clown Anemonefishes, Amphiprion ocellaris|publisher=The MarineBio Conservation Society|work=Marinebio|accessdate=2011-12-19}} 9. ^{{cite web | title = Anemonefish oxygenate their anemone hosts at night | url = http://jeb.biologists.org/content/216/6/970 | publisher = The Journal of Experimental Biology |author1=Joseph T. Szczebak |author2=Raymond P. Henry |author3=Fuad A. Al-Horani |author4=Nanette E. Chadwick | date = 2012-11-03 | accessdate = 2013-09-15 }} 10. ^Mebs, D. 1994. "Anemonefish symbiosis: Vulnerability and Resistance of Fish to the Toxin of the Sea Anemone." Toxicon. Vol. 32(9):1059–1068. 11. ^Lieske, E.; and R. Myers (1999). Coral Reef Fishes. {{ISBN|0-691-00481-1}} 12. ^{{cite web | author=Patzner, R.A. | url=http://www.patzner.sbg.ac.at/Gobiidae/Gob_inc.html | title=Gobius incognitus | date=5 July 2017 | accessdate=10 January 2018 }} 13. ^Fretwell, K.; and B. Starzomski (2014). Painted greenling. Biodiversity of the Central Coast. Retrieved 29 January 2015. 14. ^Clownfish Breeding for Beginners by Jeff Hesketh of Mad Hatter's Reef 15. ^{{cite web | title = Clown Anemofish | url = http://www.flmnh.ufl.edu/fish/gallery/descript/FalseClownAnemone/FalseClownAnemone.html| publisher = Florida Museum of Natural History | author = Stephanie Boyer | accessdate = 2013-09-15 }} 16. ^1 {{cite web|title=Reproductive Behavior of the Anemonefish Amphiprion melanopus on Guam |url=http://www.denix.osd.mil/nr/crid/Coral_Reef_Iniative_Database/Guam_files/Ross,%201978.pdf |publisher=Copeia |author=Robert M. Ross |date=1978-02-10 |accessdate=2013-09-15 |deadurl=yes |archiveurl=https://web.archive.org/web/20120925145902/http://www.denix.osd.mil/nr/crid/Coral_Reef_Iniative_Database/Guam_files/Ross%2C%201978.pdf |archivedate=2012-09-25 }} 17. ^{{cite journal | title = Does the presence of non-breeders enhance the fitness of breeders? An experimental analysis in the clown anemonefish Amphiprion percula | journal = Behavioral Ecology and Sociobiology| volume = 57| pages = 23–31| doi = 10.1007/s00265-004-0833-2| author = Peter Buston | date = 2004-08-18 }}{{Dead link|date=September 2018 |bot=InternetArchiveBot |fix-attempted=yes }} 18. ^{{cite web | title = Determining the level of parental care relating fanning behavior of five species of clownfishes in captivity | url = http://nopr.niscair.res.in/bitstream/123456789/14876/1/IJMS%2041(5)%20430-441.pdf | publisher = Indian Journal of Geo-Marine Sciences |author1=Swagat Ghosh |author2=T. T. Ajith Kumar |author3=T. Balasubramanian | date = 2011-08-04 | accessdate = 2013-09-15 }} 19. ^{{FishBase genus|genus=Amphiprion|year=2011|month=December}} 20. ^{{FishBase genus|genus=Premnas|year=2011|month=December}} 21. ^{{cite book|last=Dhaneesh|first=K.V.|author2=R. Vinoth|author3= Swagat Gosh|author4= M. Gopi|author5= T.T. Ajith Kumar|author6= T. Balasubramanian|title=Hatchery Production of Marine Ornamental Fishes: An Alternate Livelihood Option for the Island Community at Lakshadweep|journal=Climate Change and Island and Coastal Vulnerability|year=2013|volume=17|pages=253–265|doi=10.1007/978-94-007-6016-5_17|editor1-first=J.|editor1-last=Sundaresan|isbn=978-94-007-6015-8}} 22. ^{{cite book|title=From ocean to aquarium: A global trade in marine ornamental species|year=2003|publisher=UNEP world conservation and monitoring centre (WCMC)|pages=1–64|url=http://www.unep.org/pdf/from_ocean_to_aquarium_report.pdf|author=Taylor, M.|author2=Razak, T.|author3=Green, E.|last-author-amp=yes|accessdate=18 April 2013}} 23. ^{{cite journal|last=Shuman|first=Craig|author2=Gregor Hodgson |author3=Richard F. Ambrose |title=Population impacts of collecting sea anemones and anemonefish for the marine aquarium trade in the Philippines|journal=Coral Reefs|year=2005|volume=24|issue=4|pages=564–573|doi=10.1007/s00338-005-0027-z |url=https://www.researchgate.net/publication/226522145|bibcode=2005CorRe..24..564S}} 24. ^{{cite journal|last=Watson|first=Craig|author2=Jeffery Hill|title=Design criteria for recirculating, marine ornamental production systems|journal=Aquacultural Engineering|year=2006|volume=34|issue=3|pages=157–162|doi=10.1016/j.aquaeng.2005.07.002}} 25. ^{{cite book|last=Hall|first=Heather|title=Marine Ornamental Species: Collection, Culture and Conservation|year=2003|publisher=Wiley-Blackwell|isbn=978-0-8138-2987-6|pages=303–326|authorlink=The role of public aquariums in the conservation and stability of the marine ornamentals trade|author2=Douglas Warmolts|editor=James C. Cato|editor2=Christopher L. Brown|chapter=23}} 26. ^{{cite book |last=Tullock |first1=John |url=https://books.google.com/books?id=NWZHcIrhEiQC&dq |title=Clownfish and Sea Anemones |edition=illustrated |publisher=Barron's Educational Series |year=1998 |pages=11–22 |accessdate=2015-05-11 |isbn=9780764105111 }} 27. ^{{cite web|last1=Fatherree|first1=James W|title=Aquarium Fish: On the Clownfishes' Range of Hosts|url=http://www.advancedaquarist.com/2014/3/fish2|website=Advanced Aquarist|accessdate=31 December 2016}} 28. ^{{cite journal|author=Daphne Gail Fautin |year=1991 |title=The anemonefish symbiosis: what is known and what is not |journal=Symbiosis |volume=10 |pages=23–46 |url=http://www.nhm.ku.edu/inverts/pdf/Fautin_anemonefishsymbiosis_1991.pdf |deadurl=yes |archiveurl=https://web.archive.org/web/20120525134758/http://www.nhm.ku.edu/inverts/pdf/Fautin_anemonefishsymbiosis_1991.pdf |archivedate=2012-05-25 |df= }} 29. ^{{cite book |author=Ronald L. Shimek |year=2004 |page=83 |title=Marine Invertebrates |publisher=T.F.H. Publications |location=Neptune City, NJ |isbn=978-1-890087-66-1}} 30. ^{{cite web|url=http://www.rottentomatoes.com/m/finding_nemo/|title=Finding Nemo (2003)|accessdate=5 April 2016}} 31. ^{{cite book|url=https://books.google.com/books?id=kV9GDgAAQBAJ&pg=PA179|page=179|title=Marine Ornamental Species Aquaculture|first1=Ricardo|last1=Calado|first2=Ike|last2=Olivotto|first3=Miquel Planas|last3=Oliver|first4=G. Joan|last4=Holt|date=6 March 2017|publisher=John Wiley & Sons|via=Google Books|isbn=9780470673904}} 32. ^{{cite journal |author1=Litsios, G. |author2=Salamin, N. |title=Hybridisation and diversification in the adaptive radiation of clownfishes| journal=BMC Evolutionary Biology |year=2014 |volume=14 |pages=245 |doi=10.1186/s12862-014-0245-5 |pmid=25433367 |pmc=4264551}} 33. ^{{cite book|last=Fautin|first=Daphne G.|author2=Allen, Gerald R. |title=Field Guide to Anemone Fishes and Their Host Sea Anemones |publisher=Western Australian Museum |year=1997 |url=http://www.nhm.ku.edu/inverts/ebooks/intro.html |isbn=9780730983651 |archive-url= https://web.archive.org/web/20150414095302/http://www.nhm.ku.edu/inverts/ebooks/intro.html |archive-date=14 April 2015}} 34. ^{{cite web |url=http://www.saltcorner.com/AquariumLibrary/browsegroupspecies.php?GroupID=1 |author=Goemans, B. |title=Anemonefishes |accessdate=20 September 2015}} 35. ^{{cite journal |author1=Litsios, G. |author2=Sims, C. |author3=Wüest, R. |author4=Pearman P.B. |author5=Zimmermann, N.E. |author6=Salamin N. |title=Mutualism with sea anemones triggered the adaptive radiation of clownfishes |journal=BMC Evolutionary Biology |year=2012 |issue= 11|pages=212 |doi=10.1186/1471-2148-12-212 |volume=12 |pmid=23122007 |pmc=3532366}} 36. ^{{cite web |url=http://www.advancedaquarist.com/blog/what-we-really-know-about-the-diversity-of-clownfish-1 |author=DeAngelis, R. |title=What we really know about the diversity of Clownfish |accessdate=20 September 2015 |archive-url=https://web.archive.org/web/20150925122657/http://www.advancedaquarist.com/blog/what-we-really-know-about-the-diversity-of-clownfish-1 |archive-date=2015-09-25 |dead-url=yes |df= }} 37. ^{{cite journal |author1=van der Meer M.H. |author2=G.P. Jones |author3=J.-P.A. Hobbs |author4=L. van Herwerden| year=2012 |title=Historic hybridization and introgression between two iconic Australian anemonefish and contemporary patterns of population connectivity |journal=Ecology and Evolution |volume=2 |issue=7 |pages=1592–1604 |doi=10.1002/ece3.251|pmid=22957165 |pmc=3434915 }} References{{Reflist|33em|refs=[32][33][34][35][36][37]}} External links{{Commons category|Amphiprioninae}}{{Wikispecies|Amphiprioninae}}
4 : Pomacentridae|Symbiosis|Articles containing video clips|Fish subfamilies |
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