|Scientific Name:||Isopora cuneata|
|Species Authority:||(Dana, 1846)|
|Taxonomic Notes:||The genus Isopora was previously a subgenus but was elevated (Wallace et al. 2007).|
|Red List Category & Criteria:||Vulnerable A4ce ver 3.1|
|Assessor(s):||Aeby, G., Lovell, E.R., Richards, Z.T., Delbeek, J.T., Reboton, C. & Bass, D.|
|Reviewer(s):||Livingstone, S., Polidoro, B. & Smith, J.|
This species is widespread and common throughout its range. However, it is particularly susceptible to disease and bleaching, predation from COTS, and extensive reduction of coral reef habitat due to a combination of threats. Specific population trends are unknown but population reduction can be inferred from declines in habitat quality based on the combined estimates of both destroyed reefs and reefs at the critical stage of degradation within its range (Wilkinson 2004). Its threat susceptibility increases the likelihood of being lost within one generation in the future from reefs at a critical stage. Therefore, the estimated habitat degradation and loss of 37% over three generation lengths (30 years) is the best inference of population reduction and meets the threshold for Vulnerable under Criterion A4ce. 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 occurs in the south-west and northern Indian Ocean, the central Indo-Pacific, Australia, Southeast Asia, Japan and the East China Sea, and the oceanic west Pacific. It is also found in Samoa, Micronesia, and Indonesia (Wallace 1999). Found in the Philippines, Fiji, Madagascar, Raja Ampats (West Papua, Indonesia), Lord Howe, New Caledonia, and Papau New Guinea (Fenner pers. comm.).|
Native:American Samoa (American Samoa); Australia; British Indian Ocean Territory; Cambodia; Comoros; Fiji; Guam; India; Indonesia; Japan; Kenya; Kiribati; Madagascar; Malaysia; Maldives; Marshall Islands; Mauritius; Mayotte; Micronesia, Federated States of ; Mozambique; Myanmar; Nauru; New Caledonia; Northern Mariana Islands; Palau; Papua New Guinea; Philippines; Réunion; Samoa; Seychelles; Singapore; Solomon Islands; Somalia; Sri Lanka; Taiwan, Province of China; Tanzania, United Republic of; Thailand; Tuvalu; Vanuatu; Viet Nam; Wallis and Futuna
|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, but less so than A. palifera.
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 particularly susceptible to bleaching, disease, and other threats and therefore population decline is based on both the percentage of destroyed reefs and critical reefs that are likely to be destroyed within 20 years (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 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 all shallow, tropical reef environments, especially upper reef slopes and reef flats. It is found intertidally or just subtidally on reef flats, reef tops or submerged reefs (Wallace 1999). This species is found to 15 m depth.|
Very susceptible to crown-of-thorns starfish because of its growth form. Members of this genus have a low resistance and low tolerance to bleaching and disease, and are slow to recover. This species is known to be susceptible to bleaching (Richards pers. comm.). Susceptible to disease with a record of Black Band disease (Willis et al. 2004)
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:||Aeby, G., Lovell, E.R., Richards, Z.T., Delbeek, J.T., Reboton, C. & Bass, D. 2014. Isopora cuneata. The IUCN Red List of Threatened Species. Version 2015.2. <www.iucnredlist.org>. Downloaded on 03 September 2015.|
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