|Scientific Name:||Acropora glauca|
|Species Authority:||(Brook, 1893)|
|Red List Category & Criteria:||Near Threatened ver 3.1|
|Assessor/s:||Richards, Z., Delbeek, J.C., Lovell, E., Bass, D., Aeby, G. & Reboton, C.|
|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, disease, and crown-of-thorns starfish predation. Specific population trends are unknown but population reduction can be inferred from estimated habitat loss (Wilkinson 2004). It is widespread and uncommon throughout its range 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 19% 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) 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. This is a higher latitude species and it is unknown how these may adapt to climate change.
|Range Description:||This species is found in the south-west Indian Ocean, Raja Ampats (West Papaua, Indonesia), the central Indo-Pacific, Australia, Southeast Asia, Japan and the East China Sea, and the central Pacific. It is found in Madagascar, Sarawak, and Lord Howe (Fenner pers. comm.). It is in Oman, Bangladesh, PNG, Fiji, and American Samoa (Wallace 1999).|
Native:American Samoa (American Samoa); Australia; Bangladesh; Cook Islands; Fiji; French Polynesia; India; Indonesia; Japan; Kiribati; Madagascar; Malaysia; Mozambique; Myanmar; New Caledonia; Oman; Papua New Guinea; Philippines; Pitcairn; Samoa; South Africa; Taiwan, Province of China; Thailand; Yemen
|FAO Marine Fishing Areas:||
Indian Ocean – eastern; Indian Ocean – western; Pacific – eastern central; Pacific – northwest; Pacific – southwest; Pacific – western central
|Range Map:||Click here to open the map viewer and explore range.|
This species is common in subtropical locations and rare elsewhere. It was found at 2 of 6 regions in Indonesia (Wallace et al. 2001).
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:||This species occurs in shallow, tropical reef environments. It is found on rocky foreshores of subtropical locations, subtidal on reef tops, and upper slopes (Wallace 1999). This species is found from 5-20 m.|
Members of this genus have a low resistance and low tolerance to bleaching and disease, and are slow to recover.
Acanthaster planci, the crown-of-thorns starfish, has been observed preferentially preying upon corals of the genus Acropora (Colgan 1987). Crown-of-thorns starfish (COTS) (Acanthaster planci) are found throughout the Pacific and Indian Oceans, and the Red Sea. These starfish voracious predators of reef-building corals, with a preference for branching and tabular corals such as Acropora species. Populations of the crown-of-thorns starfish have greatly increased since the 1970s and have been known to wipe out large areas of coral reef habitat. Increased breakouts of COTS has become a major threat to some species, and have contributed to the overall decline and reef destruction in the Indo-Pacific region. The effects of such an outbreak include the reduction of abundance and surface cover of living coral, reduction of species diversity and composition, and overall reduction in habitat area.
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.
|Citation:||Richards, Z., Delbeek, J.C., Lovell, E., Bass, D., Aeby, G. & Reboton, C. 2008. Acropora glauca. In: IUCN 2012. IUCN Red List of Threatened Species. Version 2012.2. <www.iucnredlist.org>. Downloaded on 18 May 2013.|
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