|Scientific Name:||Pectinia teres|
|Species Authority:||Nemenzo and Montecillo 1981|
|Red List Category & Criteria:||Near Threatened 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). It is not widespread and is uncommon throughout its range. The estimated habitat loss of 26% 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 on lower reef slopes (Wilkinson 2004). This inference of population reduction over three generation lengths (30 years) does not meet the threshold of a threat category. However, since this population reduction estimate is close to a threatened threshold, and because this species is moderately susceptible to a number of threats, it is likely to be one of the species lost on some reefs currently at the critical stage of degradation and therefore is Near Threatened. Predicted threats from climate change and ocean acidification make it important to reassess this species in 10 years or sooner, particularly if the species is actually observed to disappear from reefs currently at the critical stage of reef degradation.
|Range Description:||In the Indo-West Pacific, this species is found in Sri Lanka, the central Indo-Pacific, north and west Australia, South-east Asia, southern Japan, the South China Sea, and north and east Papua New Guinea. The Solomons (TNC).|
Native:Australia; India; Indonesia; Japan; Malaysia; Myanmar; Papua New Guinea; Philippines; Singapore; Solomon Islands; Sri Lanka; Taiwan, Province of China; Thailand
|FAO Marine Fishing Areas:||
Indian Ocean – eastern; Pacific – northwest; Pacific – western central
|Range Map:||Click here to open the map viewer and explore range.|
This is an uncommon species.
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. Follow the link below for further details on population decline and generation length estimates.
|Habitat and Ecology:||
It is found on lower reef slopes and enclosed embayments, especially with turbid water. Pectinia colonies occasionally reach 1 m or more in diameter (Wood 1983). P. teres grows to around 30 cm (Fenner pers. comm.). This species is found to 30 m.
Pectinia occurs in most reef habitats, both in shallow and deep areas (Wood 1983). This genus is typically conspicuous (Veron 1995). P. teres is one of the less conspicuous Pectinia species.
In the Great Barrier Reef, Pectinia showed high susceptibility to bleaching (Baird and Marshall 2000). There is no information on bleaching response in the WIO.
In Lampung, Southern Sumatra Pectinia is in the top 25 genera collected for the aquarium trade (Terangi Indonesian Coral Reef Foundation, unpublished data).
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.
Coral disease has emerged as a serious threat to coral reefs worldwide and a major cause of reef deterioration (Weil et al. 2006). The numbers of diseases and coral species affected, as well as the distribution of diseases have all increased dramatically within the last decade (Porter et al. 2001, Green and Bruckner 2000, Sutherland et al. 2004, Weil 2004). Coral disease epizootics have resulted in significant losses of coral cover and were implicated in the dramatic decline of acroporids in the Florida Keys (Aronson and Precht 2001, Porter et al. 2001, Patterson et al. 2002). In the Indo-Pacific, disease is also on the rise with disease outbreaks recently reported from the Great Barrier Reef (Willis et al. 2004), Marshall Islands (Jacobson 2006) and the northwestern Hawaiian Islands (Aeby 2006). Increased coral disease levels on the GBR were correlated with increased ocean temperatures (Willis et al. 2007) supporting the prediction that disease levels will be increasing with higher sea surface temperatures. Escalating anthropogenic stressors combined with the threats associated with global climate change of increases in coral disease, frequency and duration of coral bleaching and ocean acidification place coral reefs in the Indo-Pacific at high risk of collapse.
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 the species’ range fall within Marine Protected Areas.
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., MPAs, 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. Recommended conservation measures include population surveys to monitor the effects of collecting for the aquarium trade, especially in Indonesia.
Aeby, G.S., Work, T., Coles, S., and Lewis, T. 2006. Coral Disease Across the Hawaiian Archipelago. EOS, Transactions, American Geophysical Union 87(36): suppl.
Aronson, R.B. and Precht, W.F. 2001 b. White-band disease and the changing face of Caribbean coral reefs. Hydrobiologia 460: 25-38.
Baird, A.H. and Marshall, P.A. (eds). 2000. Patterns of recovery following mass bleaching of corals on the Great Barrier Reef. In: Hopley, D., Hopley, P., Tamelander, J., and Done, T. (eds), Abstracts, Ninth International Coral Reef Symposium, International Society for Reef Studies.
Bruno, J.F., Selig, E.R., Casey, K.S., Page, C.A., Willis, B.L., Harvell, C.D., 2007. Thermal Stress and Coral Cover as Drivers of Coral Disease Outbreaks Sweatman, H., and Melendy, A.M. PLoS Biol 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.
Jacobson, D.M. 2006. Fine Scale Temporal and Spatial Dynamics of a Marshall Islands Coral Disease Outbreak: Evidence for Temperature Forcing. EOS, Transactions, American Geophysical Union 87(36): suppl.
Patterson, K.L., Porter, J.W., Ritchie, K.B., Polson, S.W., Mueller E., Peters, E.C., Santavy, D.L., Smith, G.W. 2002. The etiology of white pox, a lethal disease of the Caribbean elkhorn coral, Acropora palmata. Proc Natl Acad Sci 99: 8725-8730.
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.
Pratchett, Morgan S. 2007. Feeding Preferences of Acanthaster planci (Echinodermata: Asteroidea) under Controlled Conditions of Food Availability. Pacific Science 61(1): 113-120.
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. 1995. Corals in space and time: the biogeography and evolution of the Scleractinia. Australian Institute of Marine Science, Cape Ferguson, Townsville, Queensland.
Veron, J.E.N. 2000. Corals of the World. Australian Institute of Marine Science, Townsville.
Wallace, C. C. 1999. Staghorn Corals of the World: a revison 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 E. Dinsdale. 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.
Wood, Dr. Elizabeth M. 1983. Reef Corals of the World: Biology and Field Guide. T.F.H. Publications Inc., Ltd., Hong Kong.
|Citation:||Sheppard, A., Fenner, D., Edwards, A., Abrar, M. & Ochavillo, D. 2008. Pectinia teres. The IUCN Red List of Threatened Species. Version 2014.3. <www.iucnredlist.org>. Downloaded on 30 March 2015.|
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