Overview
Comprehensive Description
Epibulus insidiator, the sling-jaw wrasse, is a spectacular coral reef fish that exhibits an extraordinary ability to protrude its jaws during feeding. This fish can rapidly protrude both upper and lower jaws to an extreme degree, extending the length of the head by 65% to capture evasive prey such as other fishes and small invertebrates. The sling-jaw is a member of the diverse and colorful fish family Labridae (the wrasses) and is closely related to the maori wrasses of the genus Cheilinus. The sling-jaw wrasse is among the most widely distributed coral reef fishes, occurring on coral reefs throughout the tropical Pacific from the Northwest Hawaiian Islands to the Western Pacific, Indian Ocean, and Red Sea.
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Biology
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Randall, J.E., G.R. Allen and R.C. Steene 1990 Fishes of the Great Barrier Reef and Coral Sea. University of Hawaii Press, Honolulu, Hawaii. 506 p. (Ref. 2334)
http://www.fishbase.org/references/FBRefSummary.php?id=2334&speccode=13770
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Distribution
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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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Range Description
Records from the main Hawaiian islands are based on single individuals recorded in O'ahu and Lanai and are considered waifs (Randall 2007). In this region, reproducing populations are known only in Johnston Atoll and the central part of the northwestern Hawaiian Islands.
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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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Randall, J.E. (1992). Red Sea Reef Fishes. Immel Publishing.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6091
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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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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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Smith, J.L.B. (1956). The fishes of Aldabra. Part VI. Ann. Mag. Nat. Hist 12 (9): 817-829
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5924
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Edwards, A. & J. Rosewell (1981). Vertical zonation of coral reef fishes in the Sudanese Red Sea. Hydrobiologia 79, 21- 31.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6095
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One of the most widespread of wrasses, this species inhabits coral reefs of the Red Sea, Indian Ocean, and the entire Western and Central Pacific region, reaching Hawaii and the Tuamotu Archipelago to the east.
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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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Size
Max. size
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Westneat, M.W. 2001 Labridae. Wrasses, hogfishes, razorfishes, corises, tuskfishes. p. 3381-3467. 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. 9823)
http://www.fishbase.org/references/FBRefSummary.php?id=9823&speccode=4844
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Epibulus insidiator diagnostic features
Diagnostic characters: Body moderately deep, maximum depth greater than length of head; dorsal profile of head convex in front of dorsal fin, a slight concavity above and before eye; head forming a broadly acute angle; jaws extremely protrusible, capable of being extended forward more then half the length of the head; 2 large canines situated anteriorly in each jaw; no enlarged tooth at rear of upper jaw; dorsal fin continuous, with 9 spines and 10 (rarely 11) soft rays, the spines and anterior soft rays of similar length; anal fin with 3 spines and 8 (rarely 9) soft rays; pectoral fins with 2 unbranched and 10 branched rays; pelvic fins filamentous in adults; caudal fin slightly rounded to truncate, the corners produced to form filamentous lobes in adults. Lateral line interrupted below posterior portion of dorsal fin, with a total of 22 or 23 pored scales. Scales reaching well onto bases of dorsal and anal fins; scales in front of dorsal fin extending forward to above eye; cheek and opercle scaled; lower jaw without scales.
Colour: overall brown or occasionally yellow; dorsal fin with several horizontal dark brown stripes and a black spot between first 2 spines; dark vertical bar on each scale; juveniles brown with several dark-edged, narrow, white bars and an ocellated black spot on anal fin and on rear of dorsal fin; large terminal phase males with whitish cheeks and nape, and reddish blotch of colour dorsally in front of dorsal fin origin.
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Diagnostic Description
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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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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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Lieske, E. and R. Myers 1994 Collins Pocket Guide. Coral reef fishes. Indo-Pacific & Caribbean including the Red Sea. Haper Collins Publishers, 400 p. (Ref. 9710)
http://www.fishbase.org/references/FBRefSummary.php?id=9710&speccode=13770
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Habitat and Ecology
Epibulus insidiator male colour was observed to intensify during courtship (Colin and Bell 1991). Males swam with caudal fin collapsed and tilted up and the anal fin folded and extended down. Males can revert to normal colour pattern when disturbed. The territory sizes of males were approximately 500-1,000 m2 and females seemed to have home ranges within this territory. Spawning occurred after or near high tide. It is sexually dimorphic with the size of male larger than the female. This species spawned in harem with males patrolling territory. Spawning ascent distance was about two to three m. Females were reported to lead the spawning. Spawning activities were found in March, April, May, July, September and October. The shape of the eggs is almost spherical.
Systems
- Marine
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Water temperature and chemistry ranges based on 150 samples.
Environmental ranges
Depth range (m): 0.61 - 1800
Temperature range (°C): 25.709 - 29.336
Nitrate (umol/L): 0.047 - 1.251
Salinity (PPS): 32.019 - 36.148
Oxygen (ml/l): 4.130 - 4.802
Phosphate (umol/l): 0.055 - 0.415
Silicate (umol/l): 0.910 - 5.501
Graphical representation
Depth range (m): 0.61 - 1800
Temperature range (°C): 25.709 - 29.336
Nitrate (umol/L): 0.047 - 1.251
Salinity (PPS): 32.019 - 36.148
Oxygen (ml/l): 4.130 - 4.802
Phosphate (umol/l): 0.055 - 0.415
Silicate (umol/l): 0.910 - 5.501
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
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From 1 to 42 meters.
Habitat: reef-associated.
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Habitat, biology and fisheries:
The sling-jaw is found on coral reefs of both exposed and protected areas to depths of 5-40m. It feeds upon small fishes, shrimps, and crabs which it can occasionally be seen capturing with its incredibly protrusive jaws. Large individuals are caught on hook and line, by spear, and are occasionally found in fish markets. The yellow phase is often captured for the aquarium trade, but fades to the more typical brown colour rendering it without commercial value.
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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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Life History and Behavior
Life Cycle
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Thresher, R.E. 1984 Reproduction in reef fishes. T.F.H. Publications, Inc. Ltd., Neptune City, New Jersey. 399 p. (Ref. 240)
http://www.fishbase.org/references/FBRefSummary.php?id=240&speccode=1263
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Evolution and Systematics
Functional Adaptations
Functional adaptation
The snout of the sling-jaw wrasse captures prey using multibar linkages to shoot its jaw out at high speed.
"Nonetheless, the jaw mechanism of even a fancy snake looks simple next to what some fish do with multibar linkages in their heads (Westneat 1991). The most extreme must be the sling-jaw wrasse, Epibulus insidiator, which shoots out an otherwise unnoticeable snout to snag prey. According to Westneat and Wainwright (1989), who've analyzed the biomechanics of the system, this wrasse can protrude its jaw by a length equal to 65 percent of normal head length. Protrusion takes only about a thirtieth of a second; acceleration exceeds 100 meters per second squared, or 10 g; and snout speed hits 2.3 meters per second, or over 5 miles per hour. The components--bones, ligaments, and muscle--may be ordinary, but their arrangement is anything but." (Vogel 2003:401)
"Epibulus insidiator (Pallas) possesses the most extreme jaw protrusion ever measured in fishes. Biomechanical models of the mechanisms of jaw protrusion and hyoid depression in Epibulus are proposed and tested. The models are designed using principles of four-bar linkages from engineering theory. The models calculate the geometry of the feeding mechanisms from morphometric data on cranial anatomy. Predictions made from the models about the feeding kinematics of Epibulus are tested by comparison with kinematic data. The model of the jaw mechanism is accurate in predicting the unique feeding mechanics of the jaws of Epibulus for most relationships between kinematic variables. A model of simultaneous cranial elevation and sternohyoideus muscle contraction is accurate in predicting hyoid depression during feeding. Biomechanical considerations limit the number of possible pathways of evolution of the jaw mechanism of Epibulus from that of its closest labrid relatives." (Westneat 1991:159)
Watch video
Learn more about this functional adaptation.
- Steven Vogel. 2003. Comparative Biomechanics: Life's Physical World. Princeton: Princeton University Press. 580 p.
- Westneat, MW. 1991. Linkage biomechanics and evolution of the unique feeding mechanism of Epibulus insidiator (Labridae: Teleostei). Journal of Experimental Biology. 159: 165-184.
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Epibulus insidiator
There are 17 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: Epibulus insidiator
Public Records: 7
Specimens with Barcodes: 19
Species With Barcodes: 1
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Conservation
Conservation Status
IUCN Red List Assessment
Red List Category
Red List Criteria
Version
Year Assessed
Assessor/s
Reviewer/s
Contributor/s
Justification
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Trends
Population
This species was described as common in northwest Madagascar (McKenna and Allen 2005) and Enewetak Atoll, Marshall Islands (Colin and Bell 1991).
In Fiji, a total of 230 individuals were counted in various UVC surveys with body sizes of 4-30 cm TL (M. Kulbicki pers. comm. 2008).
In New Caledonia, a total of 524 individuals were counted in various UVC surveys with body sizes of 6-40 cm TL. In 15 stations, a total of 29 individuals were caught with total body weight of 2,127 g (M. Kulbicki pers. comm. 2008).
In French-Polynesia, a total of 210 individuals were counted in various UVC surveys with body sizes of 3-33 cm TL (M. Kulbicki pers. comm. 2008).
In Tonga, a total of 130 individuals were counted in various UVC surveys with body sizes of 6-35 cm TL (M. Kulbicki pers. comm. 2008).
On the east coast of Peninsular Malaysia, an estimated mean density of 4.3 individuals from twenty 50 m X 5 m transects was recorded in underwater fish visual surveys (Yusuf et al. 2002).
Population Trend
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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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Management
Conservation Actions
In Madagascar
This species was reported from the Natural Reserve of the Glorieuses Islands (Durville et al. 2003). Labrids are not major catches in the reef fishes surrounding the south-west Madagascar in 1997 (Laroche et al. 1997), and catch-per-unit-effort is still relatively high in these fishing grounds. There are two marine protected areas, with no-take zones, located in the northwest region of Madagascar (McKenna and Allen 2005). This species was commonly sighted during a rapid biodiversity survey in northwest Madagascar, and is likely protected within the protected areas (McKenna and Allen 2005).
In Mozambique
There is no known fishery management or regulations on this species in Mozambique. There is a 22 km2 marine reserve, two national parks and one wildlife sanctuary where coastal waters are protected (Francis et al. 2002, Wells et al. 2007). A fish survey in 2000 at various locations including marine protected areas did not record this species (Motta et al. 2002). The occurrence of this species within these areas needs further investigation.
In Australia
Queensland
Marine parks are established within Queensland including the well-know Great Barrier Reef. Marine parks are zoned for different purposes and offer different levels of protection from recreational and commercial fishing activities (Environmental Protection Agency 2008). For fishery management, a minimum size of 25 cm TL and a bag limit of 5 fish apply to all wrasses (Department of Primary Industries and Fisheries 2008a). There are three, nine-day closure to the taking of all coral reef fishes in Queensland east coast waters, which are in October, November and December each year around the new moon phase (Department of Primary Industries and Fisheries 2008b). There is no specific management measure or regulation on this species in commercial food fish fishery.
This species is collected as part of the international aquarium fish trade. Both recreational and licensed commercial aquarium fish collectors are allowed to operate within certain zones in the Great Barrier Reef (Ryan and Clarke 2005). While SCUBA and hookah are allowed for commercial collectors, recreational collectors can only use mask and snorkel for collecting aquarium fish. There are also gear restrictions (only by hands, small fishing lines or seine-nets) and bag limits (20 fish per person) on aquarium fish collection for both recreational and commercial collectors (Ryan and Clarke 2005). There is no specific management or regulation on E. insidiator.
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Relevance to Humans and Ecosystems
Benefits
Importance
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Burgess, W.E., H.R. Axelrod and R.E. Hunziker III 1990 Dr. Burgess's atlas of marine aquarium fishes. T.F.H. Publications, Inc., Neptune City, New Jersey. 768 p.
http://www.fishbase.org/references/FBRefSummary.php?id=9210
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Gomon, M.F. and J.E. Randall 1984 Labridae. In W. Fischer and G. Bianchi (eds.) FAO species identification sheets for fishery purposes. Western Indian Ocean fishing area 51. Vol. 2. (Ref. 5374)
http://www.fishbase.org/references/FBRefSummary.php?id=5374&speccode=14328
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Wikipedia
Epibulus insidiator
The slingjaw wrasse, Epibulus insidiator, is a labrid best known for its remarkable degree of jaw protrusion.[3][4]
Notes
- ^ ITIS
- ^ BioLib
- ^ Froese, Rainer, and Daniel Pauly, eds. (2009). "Epibulus insidiator" in FishBase. July 2009 version.
- ^ Bone Q and Moore RH (2008) Biology of Fishes, Page 200. Taylor & Francis Group. ISBN 978-0-415-37562-7
Unreviewed



