Acanthurus auranticavus

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Taxonomy [top]

Kingdom Phylum Class Order Family
ANIMALIA CHORDATA ACTINOPTERYGII PERCIFORMES ACANTHURIDAE

Scientific Name: Acanthurus auranticavus
Species Authority: Randall, 1956
Common Name/s:
English Orange-socket Surgeonfish, Ring-tail Surgeon

Assessment Information [top]

Red List Category & Criteria: Least Concern ver 3.1
Year Published: 2012
Date Assessed: 2010-05-03
Assessor/s: Russell, B., Nanola, C., Choat, J.H., Stockwell, B., McIlwain, J., Clements, K.D., Rocha, L.A., Abesamis, R. & Myers, R.
Reviewer/s: Davidson, L., Edgar, G. & Kulbicki, M.
Justification:
Acanthurus auranticavus is widespread and generally uncommon. It is captured for food but is not targeted in most of its range. There are no major threats known for this species and it occurs in a number of marine protected areas in parts of its distribution. It is therefore listed as Least Concern.

Geographic Range [top]

Range Description:Acanthurus auranticavus is found from the Philippines, Indonesia, Great Barrier Reef, Australia, Maldives and Seychelles (Randall 2001a). It was reported from Ashmore, Scott and Rowley Shoals (J.H. Choat pers. comm. 2010), Malaysia (Mohsin et al. 1993), Samoa (Wass 1984), western Solomon Islands (Aswani and Lauer 2006) and Papua New Guinea (Allen et al. 2003). It was recently recorded from Christmas Island (J.H. Choat pers. comm. 2010). Records from Samoa and Viet Nam need to be verified (K.D. Clements pers. comm. 2010).
Countries:
Native:
American Samoa (American Samoa); Australia; British Indian Ocean Territory (Chagos Archipelago); Brunei Darussalam; Christmas Island; Fiji; Indonesia; Malaysia; Maldives; Marshall Islands; Papua New Guinea; Philippines; Seychelles; Singapore; Thailand; Timor-Leste
FAO Marine Fishing Areas:
Native:
Indian Ocean – eastern; Indian Ocean – western; Pacific – eastern central; Pacific – western central
Range Map:Click here to open the map viewer and explore range.

Population [top]

Population: Acanthurus albipectoralis has been recorded as abundant in deep stations at the Nha Trang Bay Marine Protected Area (MPA) (Nguyen and Phan 2008). This deep water record from Viet Nam is doubtful on the basis that this species has only been observed on reef flats and reef crests in other parts of its range (i.e., Great Barrier Reef) and similar species (A. blochii, A. grammoptilus and A. xanthopterus) have not been observed during the Viet Nam survey (K.D. Clements pers. comm. 2010). Visual census surveys along Aceh coast, Indonesia, recorded fish densities of 4 individuals/750 m2 at Teluk Pelabuhan (FMIPA 2007).
Population Trend: Unknown

Habitat and Ecology [top]

Habitat and Ecology: Acanthurus auranticavus inhabits shallow reefs, both in lagoons and outer reef areas. It is generally associated with hard substrata (K.D. Clements pers. comm. 2010). It is often encountered in feeding aggregations, sometimes consisting of more than 30 individuals (Randall 2001a). It was recorded as a major resident species on shallow inner lagoon reefs, mid-depth inner lagoon reef and lagoon pool and reef channel in the Baraulu MPA, Western Solomon Islands (Aswani and Lauer 2006). A. auranticavus feeds on detritus and sedimentary material (Choat  et al. 2004). Maximum age is 30 years (Choat and Robertson 2002). It is classified as a grazer/detritivore (Choat and Bellwood pers. obs. in Green and Bellwood 2009).

The sexes are separate among the acanthurids (Reeson 1983). Acanthurids do not display obvious sexual dimorphism, males assume courtship colours (J.H. Choat pers. comm. 2010).
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Systems: Marine

Threats [top]

Major Threat(s): There are no major threats known for this species.

Surgeonfishes show varying degrees of habitat preference and utilization of coral reef habitats, with some species spending the majority of their life stages on coral reef while others primarily utilize seagrass beds, mangroves, algal beds, and /or rocky reefs. The majority of surgeonfishes are exclusively found on coral reef habitat, and of these, approximately 80% are experiencing a greater than 30% loss of coral reef area and degradation of coral reef habitat quality across their distributions. However, more research is needed to understand the long-term effects of coral reef habitat loss and degradation on these species' populations. Widespread coral reef loss and declining habitat conditions are particularly worrying for species that recruit into areas with live coral cover, especially as studies have shown that protection of pristine habitats facilitate the persistence of adult populations in species that have spatially separated adult and juvenile habitats (Comeros-Raynal et al. 2012).

Conservation Actions [top]

Conservation Actions: There are no species-specific conservation measures in place for this species. Its distribution overlaps several marine protected areas in parts of its range.

Bibliography [top]

Allen, M., Kinch, J. and Werner, T. 2003. Living Coral Reef Resources of Milne Bay Province, Papua New Guinea. In: G.R. Allen, J. P. Kinch, S. A. McKenna, and P. Seeto (eds), A Rapid Marine Biodiversity Assessment of Milne Bay Province, Papua New Guinea- Survey II (2000), pp. 56-74. Conservation International, Washington, D.C.

Aswani, S. and Lauer, M. 2006. Benthic mapping using local aerial photo interpretation and resident taxa inventories for designing marine protected areas. Environmental Conservation 33(3): 263–273.

Choat, J.H., Robbins, W.D. and Clements, K.D. 2004. The trophic status of herbivorous fishes on coral reefs. Marine Biology 145: 445-454.

Comeros-Raynal, M.T., Choat, J.H., Polidoro, B., Clements, K.D., Abesamis, R., Craig, M.T., Lazuardi, M.E., McIlwain, J., Muljadi, A., Myers, R.F., et al.. 2012. The likelihood of extinction of iconic and dominant components of coral reefs: the parrotfishes and surgeonfishes. PLoS ONE http://dx.plos.org/10.1371/journal.pone.0039825.

Faculty of Mathematic and Natural Science (FMIPA). 2007. Community-drive coral conservation in Aceh, Indonesia. Final Report, 2007. A Report to Rufford Small Grant (for Nature Conservation). Faculty of Mathematic and Natural Science (FMIPA) University of Syiah Kuala.

Green, A.L. and Bellwood, D.R. 2009. Monitoring functional groups of herbivorous reef fishes as indicators of coral reef resilience ? A practical guide for coral reef managers in the Asia Pacific region. IUCN, Gland, Switzerland.

IUCN. 2012. IUCN Red List of Threatened Species (ver. 2012.2). Available at: http://www.iucnredlist.org. (Accessed: 17 October 2012).

Mohsin, A.K.M., Ambak, M.A. and Salam, M.N.A. 1993. Malay, English, and scientific names of the fishes of Malaysia. Faculty of Fisheries and Marine Science, Universiti Pertanian Malaysia, Selangor Darul Ehsan, Malaysia, Occasional Publication No. 11. Universiti Pertanian Malaysia, Selangor Darul Ehsan, Malaysia.

National Park of American Samoa. 2008. Fishes of National Park of American Samoa Checklist of Fishes Family Name Listing. Available at: http://www.botany.hawaii.edu/basch/uhnpscesu/htms/npsafish/family/acanthur.htm. (Accessed: 21 April).

Nguyen, L.V. and Phan, H.K. 2008. Distribution and factors influencing on structure of reef fish communities in Nha Trang Bay Marine Protected Area, South-Central Vietnam. Environmental Biology of Fishes 82: 309-324.

Randall, J.E. 2001a. Surgeonfishes of the world. Mutual Publishing and Bishop Museum Press, Hawai'i, Honolulu, Hawaii.

Reeson, P.H. 1983. The biology, ecology and bionomics of the surgeonfishes, Acanthuridae. In: J.L. Munro (ed.), Caribbean coral reef fishery resources, pp. 178-190.

Wass, R.C. 1984. An annotated checklist of the fishes of American Samoa. NOAA Technical Report NMFS SSRF-781. U.S. Dept. of Commerce, Rockville, Maryland.

Citation: Russell, B., Nanola, C., Choat, J.H., Stockwell, B., McIlwain, J., Clements, K.D., Rocha, L.A., Abesamis, R. & Myers, R. 2012. Acanthurus auranticavus. In: IUCN 2013. IUCN Red List of Threatened Species. Version 2013.2. <www.iucnredlist.org>. Downloaded on 24 April 2014.
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