|Scientific Name:||Goniopora polyformis Zou, 1980|
|Red List Category & Criteria:||Vulnerable A4c ver 3.1|
|Assessor(s):||Sheppard, A., Fenner, D., Edwards, A., Abrar, M. & Ochavillo, D.|
|Reviewer(s):||Livingstone, S., Polidoro, B. & Smith, J. (Global Marine Species Assessment)|
The most important known threat for this species is extensive reduction of coral reef habitat due to a combination of threats, however, this species is also moderately susceptible to bleaching. Specific population trends are unknown but population reduction can be inferred from estimated habitat loss (Wilkinson 2004). This species is widespread and although rare within its range, it has a low susceptibility to bleaching and disease, can be found in temperate waters, and therefore is likely to be more resilient to habitat loss and reef degradation because of an assumed large effective population size that is highly connected and/or stable with enhanced genetic variability. Therefore, the estimated habitat loss of 37% from reefs already destroyed within its range is the best inference of population reduction since it may survive in coral reefs already at the critical stage of degradation (Wilkinson 2004). This inference of population reduction over three generation lengths (30 years) is the best inference of population reduction and meets the threshold for Vulnerable Criterion A4c. It will be important to reassess this species in 10 years time because of predicted threats from climate change and ocean acidification.
|Range Description:||This species is found in the central Indo-Pacific, South-east Asia, Japan and South China Sea.|
Native:Australia; Cambodia; China; Indonesia; Japan; Malaysia; Micronesia, Federated States of ; Philippines; Singapore; Taiwan, Province of China; Thailand; Viet Nam
|FAO Marine Fishing Areas:|
Indian Ocean – eastern; Pacific – northwest; Pacific – western central
|Range Map:||Click here to open the map viewer and explore range.|
|Population:||This species is rare.|
There is no species specific population information available for this species. However, there is evidence that overall coral reef habitat has declined, and this is used as a proxy for population decline for this species. This species is more resilient to some of the threats faced by corals and therefore population decline is estimated using the percentage of destroyed reefs only (Wilkinson 2004). We assume that most, if not all, mature individuals will be removed from a destroyed reef and that on average, the number of individuals on reefs are equal across its range and proportional to the percentage of destroyed reefs. Reef losses throughout the species' range have been estimated over three generations, two in the past and one projected into the future.
The age of first maturity of most reef building corals is typically three to eight years (Wallace 1999) and therefore we assume that average age of mature individuals is greater than eight years. Furthermore, based on average sizes and growth rates, we assume that average generation length is 10 years, unless otherwise stated. Total longevity is not known, but likely to be more than ten years. Therefore any population decline rates for the Red List assessment are measured over at least 30 years. See the supplementary material for further details on population decline and generation length estimates.
|Current Population Trend:||Unknown|
|Habitat and Ecology:||This species is found in shallow reef environments, and general depths are unknown for this species.|
Goniopora is in the top five genera in the aquarium trade (Wabnitz et al. 2003). Although disease risk is likely to be low for species of this genus (Aeby pers. comm.), Goniopora species are moderately susceptible to bleaching in the western Indian Ocean (McClanahan et al. 2007), and exhibit low susceptibility in the Great Barrier Reef (Marshall and Baird 2000).
In general, the major threat to corals is global climate change, in particular, temperature extremes leading to bleaching and increased susceptibility to disease, increased severity of ENSO events and storms, and ocean acidification. In addition to global climate change, corals are threatened by a number of localized threats. Localized threats to corals include fisheries, human development (industry, settlement, tourism, and transportation), changes in native species dynamics (competitors, predators, pathogens and parasites), invasive species (competitors, predators, pathogens and parasites), dynamite fishing, chemical fishing, pollution from agriculture and industry, domestic pollution, sedimentation, and human recreation and tourism activities. The severity of these combined threats to the global population of each individual species is not known.
All corals are listed on CITES Appendix II. Parts of this species distribution fall within several Marine Protected Areas within its range.
Recommended measures for conserving this species include research in taxonomy, population, abundance and trends, ecology and habitat status, threats and resilience to threats, restoration action; identification, establishment and management of new protected areas; expansion of protected areas; recovery management; and disease, pathogen and parasite management. Artificial propagation and techniques such as cryo-preservation of gametes may become important for conserving coral biodiversity.
Having timely access to national-level trade data for CITES analysis reports would be valuable for monitoring trends this species. The species is targeted by collectors for the aquarium trade and fisheries management is required for the species, e.g., Marine Protected Areas, quotas, size limits, etc. Consideration of the suitability of species for aquaria should also be included as part of fisheries management, and population surveys should be carried out to monitor the effects of harvesting.
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Bruno, J.F., Selig, E.R., Casey, K.S., Page, C.A., Willis, B.L., Harvell, C.D., Sweatman, H., and Melendy, A.M. 2007. Thermal stress and coral cover as drivers of coral disease outbreaks. PLoS Biology 5(6): e124.
Colgan, M.W. 1987. Coral Reef Recovery on Guam (Micronesia) After Catastrophic Predation by Acanthaster Planci. Ecology 68(6): 1592-1605.
Green, E.P. and Bruckner, A.W. 2000. The significance of coral disease epizootiology for coral reef conservation. Biological Conservation 96: 347-361.
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Marshall, P.A. and Baird, A.H. 2000. Bleaching of corals on the Great Barrier ReefL differential susceptibilities among taxa. Coral Reefs 19(2): 155-163.
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Porter, J.W., Dustan, P., Jaap, W.C., Patterson, K.L., Kosmynin, V., Meier, O.W., Patterson, M.E., and Parsons, M. 2001. Patterns of spread of coral disease in the Florida Keys. Hydrobiologia 460(1-3): 1-24.
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Sutherland, K.P., Porter, J.W., and Torres, C. 2004. Disease and immunity in Caribbean and Indo-Pacific zooxanthellate corals. Marine ecology progress series 266: 273-302.
Veron, J.E.N. 2000. Corals of the World. Australian Institute of Marine Science, Townsville.
Wabnitz, C., Taylor, M., Green, E. and Razak, T. 2003. From ocean to aquarium: the global trade in marine ornamental species. UNEP World Conservation Monitoring Centre, Cambridge, U.K.
Wallace, C.C. 1999. Staghorn Corals of the World: a revision of the coral genus Acropora. CSIRO, Collingwood.
Weil, E. 2004. Coral reef diseases in the wider Caribbean. In: E. Rosenberg and Y. Loya (eds), Coral Health and Diseases, pp. 35-68. Springer Verlag, NY.
Weil, E. 2006. Coral, Ocotocoral and sponge diversity in the reefs of the Jaragua National Park, Dominican Republic. Rev. Bio. Trop. 54(2): 423-443.
Wilkinson, C. 2004. Status of coral reefs of the world: 2004. Australian Institute of Marine Science, Townsville, Queensland, Australia.
Willis, B., Page, C and Dinsdale, E. 2004. Coral disease on the Great Barrier Reef. In: E. Rosenber and Y. Loya (eds), Coral Health and Disease, pp. 69-104. Springer-Verlag Berlin Heidelberg.
|Citation:||Sheppard, A., Fenner, D., Edwards, A., Abrar, M. & Ochavillo, D. 2008. Goniopora polyformis. The IUCN Red List of Threatened Species 2008: e.T133014A3544759.Downloaded on 20 May 2018.|
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