Overview
Comprehensive Description
Biology
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Myers, R.F. 1991 Micronesian reef fishes. Second Ed. Coral Graphics, Barrigada, Guam. 298 p. (Ref. 1602)
http://www.fishbase.org/references/FBRefSummary.php?id=1602&speccode=4306
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Distribution
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MacNae, W. & M. Kalk (eds) (1958). A natural history of Inhaca Island, Mozambique. Witwatersrand Univ. Press, Johannesburg. I-iv, 163 pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6266
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Anon. (1996). FishBase 96 [CD-ROM]. ICLARM: Los Baños, Philippines. 1 cd-rom pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5909
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Anon. (2000). FishBase 2000 [CD-ROM]. ICLARM: Los Baños, Laguna, Philippines. 4 cd-roms pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6542
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Smith, J.L.B. & M.M. Smith (1963). The fishes of Seychelles. Department of Ichthyology, Rhodes University. Grahamstown.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5926
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Bock, K.R. (1996). Checklist of the reef fishes of Diani and Galu, Kenya. Journal of East African natural History 85: 5-22.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6357
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McClanahan, T.R. (1994). Kenya coral reef lagoon fish: effects of fishing, substrate complexity, and sea urchins. Coral Reefs 13: 231-241
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5911
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Letourneur, Y., M. Harmelin-Vivien & R. Galzin (1993). Impact of hurricane Firinga on fish community structure on fringing reefs of Reunion Island, S.W. Indian Ocean. Environmental Biology of Fishes 37: 109-120
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6048
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Daudi, L.N. 2010. The Role of Food Availability and Presence of Predators On Population Trends of The Sea Urchin Tripneustes Gratilla (L.) In Seagrass Beds of Watamu Marine National Park and Researve, Kenya Report No: Wiomsa/Marg-I/2010 – 06
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=164088
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Matsuura, K. 2001 Balistidae. Triggerfishes. p. 3911-3928. In K.E. Carpenter and V. Niem (eds.) FAO species identification guide for fishery purposes. The living marine resources of the Western Central Pacific. Vol. 6. Bony fishes part 4 (Labridae to Latimeriidae), estuarine crocodiles. FAO, Rome. (Ref. 9770)
http://www.fishbase.org/references/FBRefSummary.php?id=9770&speccode=9
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Geographic Range
Considered to live in the Indo-Pacific region, reef triggerfish transverse a wide variety of marine areas from thirty degrees north to south in latitude (Michael 1998). Reef triggerfish extend from the Hawaiian islands southward to Polynesia and Australia, westward through Micronesia and Melanesia, through the East Indies including the Philippines, across the Indian Ocean, to the coast of Africa and the Red Sea. More specifically, reef triggerfish occupy the Red Sea south to South Africa, east to the Hawaiian, Marquesas, and Tuamotu Islands, north to southern Japan, south to Lord Howe Island, Micronesia, and the Eastern Atlantic from Senegal to South Africa (Allen and Steen 1994).
Biogeographic Regions: australian (Native ); oceanic islands (Native ); indian ocean (Native ); pacific ocean (Native )
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Physical Description
Morphology
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Myers, R.F. 1991 Micronesian reef fishes. Second Ed. Coral Graphics, Barrigada, Guam. 298 p. (Ref. 1602)
http://www.fishbase.org/references/FBRefSummary.php?id=1602&speccode=4306
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Physical Description
A reef triggerfish is easily distinguished by its angular body, distinctive color pattern (resembling blocks of colors), fin arrangement, and characteristic dorsal spine. This forward spine on the dorsal fin lies slightly above and behind the eye. It is very strong and rigid, serving as defense adaptation. When this spine is raised, it often locks in this protective position, giving the triggerfish its name. Altogether, there are three dorsal spines, twenty-three to twenty-six dorsal softrays, twenty-one to twenty-three anal softrays, and no anal spines (Michael 1998). Considered to be sturdy and well-built, the reef triggerfish reaches a maximum length of thirty centimeters (Tinker 1982). It has a small but powerful jaw, equipped with sharp, cutting teeth. The eyes of a reef triggerfish are set atop the head, moving independently, so as to scan the reef for possible predators and prey (Hoover 1993).
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Size
Max. size
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Smith, M.M. and P.C. Heemstra 1986 Balistidae. p. 876-882. In M.M. Smith and P.C. Heemstra (eds.) Smiths' sea fishes. Springer-Verlag, Berlin. (Ref. 4420)
http://www.fishbase.org/references/FBRefSummary.php?id=4420&speccode=1311
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Diagnostic Description
Description
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Anon. (1996). FishBase 96 [CD-ROM]. ICLARM: Los Baños, Philippines. 1 cd-rom pp.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5909
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Ecology
Habitat
Environment
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Harmelin-Vivien, M.L. and J.-C. Quéro 1990 Balistidae. p. 1055-1060. In J.C. Quero, J.C. Hureau, C. Karrer, A. Post and L. Saldanha (eds.) Check-list of the fishes of the eastern tropical Atlantic (CLOFETA). JNICT, Lisbon; SEI, Paris; and UNESCO, Paris. Vol. 2. (Ref. 7348)
http://www.fishbase.org/references/FBRefSummary.php?id=7348&speccode=19
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The reef triggerfish is generally found in shallow outer reef habitats. Swimming along the bottom in search of food items, it is found on surge-swept basalt reefs. The reef triggerfish is commonly found in subtidal reef flats and protected lagoons (Hoover 1993). This marine fish usually occupies water with salinity levels ranging from 1.020 to 1.023, and water temperatures from seventy-seven to eighty degrees Fahrenheit (Tinker 1982).
Aquatic Biomes: reef ; coastal
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Water temperature and chemistry ranges based on 25 samples.
Environmental ranges
Depth range (m): 0.15 - 19
Temperature range (°C): 24.659 - 29.336
Nitrate (umol/L): 0.016 - 2.714
Salinity (PPS): 34.080 - 36.148
Oxygen (ml/l): 4.454 - 4.825
Phosphate (umol/l): 0.087 - 0.507
Silicate (umol/l): 1.073 - 4.612
Graphical representation
Depth range (m): 0.15 - 19
Temperature range (°C): 24.659 - 29.336
Nitrate (umol/L): 0.016 - 2.714
Salinity (PPS): 34.080 - 36.148
Oxygen (ml/l): 4.454 - 4.825
Phosphate (umol/l): 0.087 - 0.507
Silicate (umol/l): 1.073 - 4.612
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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Recorded at 50 meters.
Habitat: reef-associated. Blackbar triggerfish. (Linnaeus, 1758) Attains 30 cm. One of the most striking triggerfishes. The main colour features are a number of diagonal bluish-white bars on the rear of the lower body; a distinctive yellow "bridle" pattern extending from mouth to below pectoral base and enclosing a blue line at base of upper lip. Three horizontal rows of black forward curving spines on caudal peduncle, the upper two rows longer than the lower row. Caudal fin slightly rounded to double emarginate. Body white with large blackish area over much of the side of the body containing four diagonal bluish white bands from midside to anal fin. Four blue lines across interorbital and three from eye to pectoral base. Inhabits reef flats and shallow lagoons over sandy areas with rubble in 1 - 20 metres. Very territorial and when breeding defends its 'nest' on the sand very aggressively. Mostly solitary tending to dart into a crevice or hole when approached. Sleeps on its side at night and makes a whirring noise when startled. Omnivorous; feeds on algae, detritus, molluscs, worms heart urchins, corals, tunicates, foraminifera and small fishes. Indo-Pacific south to Algoa Bay in South Africa.
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Trophic Strategy
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Sano, M., M. Shimizu and Y. Nose 1984 Food habits of teleostean reef fishes in Okinawa Island, southern Japan. University of Tokyo Bulletin, no. 25. v,128p. University of Tokyo Press, Tokyo, Japan. 128 p. (Ref. 6110)
http://www.fishbase.org/references/FBRefSummary.php?id=6110&speccode=9950
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Food Habits
The reef triggerfish diet consists mainly of reef invertebrates and algae. Common food items are small crustaceans, worms, brittlestars, sea urchins, and snails. Less common dietary supplements are other fishes, corals, tunicates, forams, and eggs. Highly versatile in its feeding possibilities, the reef triggerfish will feed on a wide variety of crustaceans, molluscs, and fish. Reef triggerfish obtain their food primarily by rooting through sand or rocks (Animal World 2000; Tinker 1982).
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Life History and Behavior
Life Cycle
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Myers, R.F. 1991 Micronesian reef fishes. Second Ed. Coral Graphics, Barrigada, Guam. 298 p. (Ref. 1602)
http://www.fishbase.org/references/FBRefSummary.php?id=1602&speccode=4306
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Reproduction
Like most fishes, the reef triggerfish undergoes heterosexual reproduction, in which there are separate male and female parents. Reef fishes are egg-layers, and the eggs are externally fertilized by the male parent. Nests are built by the female parent, in which the eggs are fertilized and cared for until they hatch. The newly-hatched young are also looked after by the female parent (Hoover 1993).
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Rhinecanthus aculeatus
There are 13 barcode sequences available from BOLD and GenBank. Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species. See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
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Download FASTA File
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Statistics of barcoding coverage: Rhinecanthus aculeatus
Public Records: 13
Specimens with Barcodes: 30
Species With Barcodes: 1
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Conservation
Conservation Status
Currently abundant in many marine environments, the reef triggerfish is not presently at risk. However, major alterations are occurring in many of these habitats, carrying the potential to greatly reduce their numbers. In additon to tropical fish collectors, human population growth and the factors that accompany it pose threats to reef triggerfish, as well as other marine fishes and organisms. Though currently not at risk, other organisms in many of the reef triggerfish's habitats are being greatly reduced by abiotic factors (Dresie 1999).
US Federal List: no special status
CITES: no special status
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Threats
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IUCN 2006 2006 IUCN red list of threatened species. www.iucnredlist.org. Downloaded July 2006.
http://www.fishbase.org/references/FBRefSummary.php?id=57073
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Relevance to Humans and Ecosystems
Benefits
Importance
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Baensch, H.A. 1992 Neue Meerwasser-Praxis. Tetra Verlag, Melle, Germany. (Ref. 7309)
http://www.fishbase.org/references/FBRefSummary.php?id=7309&speccode=944
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Matsuura, K. 2001 Balistidae. Triggerfishes. p. 3911-3928. In K.E. Carpenter and V. Niem (eds.) FAO species identification guide for fishery purposes. The living marine resources of the Western Central Pacific. Vol. 6. Bony fishes part 4 (Labridae to Latimeriidae), estuarine crocodiles. FAO, Rome. (Ref. 9770)
http://www.fishbase.org/references/FBRefSummary.php?id=9770&speccode=9
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Economic Importance for Humans: Positive
Caught with drive-in nets, reef triggerfish satisfy minor commercial fisheries purposes, but have a high commercial value for aqauriums. Reef triggerfish are considered good aquarium fish, as they are hardy and easy to keep and maintain. The ability of the fish to feed upon a wide variety of items, from live to frozen and flake foods, makes it very marketable among aquariums. With no special requirements for temperature or light conditions, the reef triggerfish is relatively versatile in its ability to adapt to environmental conditions. As it is easily caught and therefore readily available for purchase, the reef triggerfish is popular, also due to its unusual markings and vibrant color (Waikiki Aquarium Education Department 1999). The reef triggerfish also has a good disposition relative to other kinds of triggerfish. The reef triggerfish is not currently highly valued as a commercial food item for the majority of the human population. However, early Hawaiians ate it infrequently. The fish was also dried and utilized as a cooking fuel by early Hawaiians when other sources of fuel were in short supply. More importantly, the reef triggerfish was used further as a substitute for pigs for some religious ceremonies (Hoover 1993).
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Wikipedia
Lagoon triggerfish
The lagoon triggerfish, (Rhinecanthus aculeatus) also known as the blackbar triggerfish, the Picassofish, and the Jamal, is a triggerfish, up to 30 cm in length, found on reefs in the Indo-Pacific region.
The Hawaiian name for the fish, humuhumunukunukuāpuaʻa (pronounced [ˈhumuˈhumuˈnukuˈnukuˈwaːpuˈwɐʔə]), also spelled humuhumu-nukunuku-a-puaʻa or just humuhumu for short (meaning "triggerfish with a snout like a pig"[1]) shares the same name with the reef triggerfish, the state fish of Hawaii.
This species has been studied in a range of research contexts, from locomotion to colour vision research.
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Behavior
Lagoon triggerfish lives in the reefs and sandy areas of coral reefs where it eats just about everything that comes along. They are always restlessly swimming around and can vigorously protect their territory against intruders, including divers, especially when guarding their eggs during reproduction season. Fortunately, their relative small size makes them much less dangerous than the larger titan triggerfish of the same family.
Mating and reproduction
Both sexes guard territories, some maintaining a territory for eight years or longer (males holding territories for significantly longer than females). A typical male territory may overlap with one to five female territories, and their mating system is described as haremic, although not much is known about this (similar mating systems are seen in other Balistidae species). If a male or female is removed or disappears their territories are soon taken over by a new fish. They reproduce repeatedly over their lifetimes.[2]
Pair-spawning takes place around sunrise, with the egg masses being attached to sand, coral rubble or algae. They hatch the same day around sunset. Although paternal care is normal in teleost fishes with external fertilization, it is the mothers in this species that guard and care for eggs until they hatch. The mother remains above the eggs for about 12–14 hours, fanning the eggs with her pectoral fins to improve aeration for perhaps 30% of the time. She chases away most fish that approach and remove other intruders like starfish by mouth. Maternal care is effective in preventing predation, and experimental removal of the mothers reduced survival to almost nothing suggesting this behaviour is adaptive. Unlike fathers, mothers forage less and over a smaller area near the egg mass while caring for the eggs. Since the males have multiple mates, caring for an egg mass would probably be more costly in terms of lost mating opportunities so maternal care is considered to be an evolutionarily stable strategy.[2]
Vision
This species has one type of single cone (SC), with visual pigment peaking in sensitivity at 413 nm (S),[3] and a double cone with different visual pigments in each member peaking at 480 nm (M) and 530 nm (L) respectively.[4] Behavioural research has provided evidence that individual members of the double cones can act as independent channels of colour information, aiding in understanding double cone function.[5] This research suggests the species has trichromatic vision, like humans.
References
| Wikimedia Commons has media related to: Rhinecanthus aculeatus |
- ^ humuhumunukunukuapuaa. The American Heritage Dictionary of the English Language: Fourth Edition. 2000
- ^ a b Kuwamura, T. (1997). "Evolution of Female Egg Care in Haremic Triggerfish, Rhinecanthus aculeatus". Ethology 103 (12): 1015–1023. doi:10.1111/j.1439-0310.1997.tb00143.x.
- ^ S = short wavelength, M = middle wavelength, L = long wavelength
- ^ Marshall, J.; Jennings, K., Goldizen, A. & Vorobyev, M. (2004). "Colour vision in reef fish". Vision down under. Brisbane, Australia: Fraser Island.
- ^ Pignatelli, V.; Champ, C.; Marshall, J.; Vorobyev, M. (2010). "Double cones are used for colour discrimination in the reef fish, Rhinecanthus aculeatus". Biology Letters (The Royal Society) 6 (4): 537–539. doi:10.1098/rsbl.2009.1010.
- "Rhinecanthus aculeatus". Integrated Taxonomic Information System. http://www.itis.gov/servlet/SingleRpt/SingleRpt?search_topic=TSN&search_value=173203. Retrieved 24 January 2006.
- Froese, Rainer, and Daniel Pauly, eds. (2005). "Rhinecanthus aculeatus" in FishBase. December 2005 version.
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