|Scientific Name:||Cantharellus jebbi Hoeksema, 1993|
|Red List Category & Criteria:||Least Concern ver 3.1|
|Assessor(s):||Hoeksema, B.W., Wood, E., Rogers, A. & Quibilan, M.C.|
|Reviewer(s):||Livingstone, S., Polidoro, B. & Smith, J.|
The most important known threat for this species is extensive reduction of coral reef habitat due to a combination of threats. Specific population trends are unknown but population reduction can be inferred from estimated habitat loss (Wilkinson 2004). It is not widespread and is rare throughout its range. The estimated habitat loss of 2% 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 and this species is Least Concern. However, because of predicted threats from climate change and ocean acidification it will be important to reassess this species in 10 years or sooner, particularly if the species is also observed to disappear from reefs currently at the critical stage of reef degradation.
|Previously published Red List assessments:|
|Range Description:||In the Indo-West Pacific, this species is found from the Bismarck Sea to Fiji including Vanuatu (Hoeksema pers. comm.). There are records for the Solomon Islands (Veron and Turak 2006).|
Native:Australia; Fiji; Guam; Indonesia; Malaysia; Micronesia, Federated States of ; Northern Mariana Islands; Palau; Papua New Guinea; Philippines; Solomon Islands; Vanuatu
|FAO Marine Fishing Areas:|
Indian Ocean – eastern; Pacific – western central; Pacific – northwest
|Range Map:||Click here to open the map viewer and explore range.|
|Population:||This species is found to be 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 on reef slopes. It is an attached and encrusting species. It is often found with a single mouth, but can also sometimes forms colonies. Approximately 5-7cm in diameter. The generation length is approximately seven years and it is a slow grower (Hoeksema 1993a). This species is found from 10-25 m.|
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:||Hoeksema, B.W., Wood, E., Rogers, A. & Quibilan, M.C. 2014. Cantharellus jebbi. The IUCN Red List of Threatened Species 2014: e.T133044A54184322.Downloaded on 14 August 2018.|
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