Articles on this page are available in 1 other language: Spanish (12) (learn more)
Overview
Brief Summary
Biology
zooxanthellate
-
UNESCO-IOC Register of Marine Organisms
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1318
Trusted
Comprehensive Description
Biology: Skeleton
More info
| Author | Skeleton? | Mineral or Organic? | Mineral | Percent Magnesium |
|---|---|---|---|---|
| Yabe and Sugiyama, 1935 | YES | MINERAL | ARAGONITE | |
| Veron, 2000 | YES | MINERAL | ARAGONITE | |
| Cairns, Hoeksema, and van der Land, 1999 | YES | MINERAL | ARAGONITE | |
| Veron and Pichon, 1982 | YES | MINERAL | ARAGONITE | |
| Faustino, 1927 | YES | MINERAL | ARAGONITE |
Trusted
Distribution
Range Description
This species is found in the southwest Indian Ocean, the northern Indian Ocean, the central Indo-Pacific, west, north and east Australia, South-east Asia, Japan and the South China Sea, and the oceanic west, central and east Pacific.
Trusted
Aldabra, Chagos, East Africa, Indo-West Pacific, Kenya, Seychelles
-
UNESCO-IOC Register of Marine Organisms
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=1318
-
Veron, J.E.N. (1986). Corals of Australia and the Indo-Pacific. Angus & Robertson Publishers, London.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5874
-
Sheppard, C.R.C. (1998). Corals of the Indian Ocean: a taxonomic and distribution database for coral reef ecologists
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6092
-
Lemmens, J.W.T.J. (1993). Reef-building corals (Cnidaria: Scleractinia) from the Watamu Marine National Reserve, Kenya; an annotated species list. Zoologische mededelingen 67, 453-465
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5875
-
Sloan, N.A., A.M. Clark & J.D. Taylor (1979). The Echinoderms of Aldabra and their habitats. Bull. Br. Mus. Nat. Hist. (Zool.) 37 (2): 81- 128.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6113
-
Sheppard, C.R.C. (1981). The Reef and Soft-substrate coral fauna of Chagos, Indian Ocean.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=6031
-
Hamilton, H.G.H. & W.H. Brakel (1984). Structure and coral reef Fauna of east african reefs. Bull. Mar. Sci. 34: 248-266
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5876
Trusted
Physical Description
Diagnostic Description
Description
Colonies are hemispherical to helmet-shaped and may be very large, with a surface of irregular humps and nodules. Colour: Usually cream or yellow but may be bright colours in shallow water. Abundance: Very common and occurs with P. lutea and P. lobata on back reef margins, lagoons and fringing reefs (Veron, 1986).
-
Veron, J.E.N. (1986). Corals of Australia and the Indo-Pacific. Angus & Robertson Publishers, London.
http://www.marinespecies.org/aphia.php?p=sourcedetails&id=5874
Trusted
Type Information
Holotype for Porites australiensis Vaughan, 1918
Catalog Number: USNM 47233
Collection: Smithsonian Institution, National Museum of Natural History, Department of Invertebrate Zoology
Preparation: Dry
Collector(s): A. Mayer
Locality: Murray Island, 620 Ft From Shore; SE Reef, Queensland, Australia, South Pacific Ocean
Catalog Number: USNM 47233
Collection: Smithsonian Institution, National Museum of Natural History, Department of Invertebrate Zoology
Preparation: Dry
Collector(s): A. Mayer
Locality: Murray Island, 620 Ft From Shore; SE Reef, Queensland, Australia, South Pacific Ocean
- Holotype: Vaughan. 1918. Publ. Carnegie Inst. Wash., Pap. Dept. Mar. Biol. 213(9): 194-195, pl.85, fig.4-6.
Trusted
Ecology
Habitat
Habitat and Ecology
Habitat and Ecology
Systems
This species occurs with P. lutea and P. lobata on back reef margins, lagoons and fringing reefs, generally to depths of 20 m. This species is commonly found from 1-15 m in the South China Sea and Gulf of Siam (Titlyanov and Titlyanova 2002).
Systems
- Marine
Trusted
Depth range based on 67 specimens in 1 taxon.
Water temperature and chemistry ranges based on 67 samples.
Environmental ranges
Depth range (m): 0 - 45
Temperature range (°C): 27.314 - 28.471
Nitrate (umol/L): 0.054 - 4.021
Salinity (PPS): 34.400 - 35.291
Oxygen (ml/l): 4.467 - 4.608
Phosphate (umol/l): 0.087 - 0.566
Silicate (umol/l): 1.130 - 2.603
Graphical representation
Depth range (m): 0 - 45
Temperature range (°C): 27.314 - 28.471
Nitrate (umol/L): 0.054 - 4.021
Salinity (PPS): 34.400 - 35.291
Oxygen (ml/l): 4.467 - 4.608
Phosphate (umol/l): 0.087 - 0.566
Silicate (umol/l): 1.130 - 2.603
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
Water temperature and chemistry ranges based on 67 samples.
Environmental ranges
Depth range (m): 0 - 45
Temperature range (°C): 27.314 - 28.471
Nitrate (umol/L): 0.054 - 4.021
Salinity (PPS): 34.400 - 35.291
Oxygen (ml/l): 4.467 - 4.608
Phosphate (umol/l): 0.087 - 0.566
Silicate (umol/l): 1.130 - 2.603
Graphical representation
Depth range (m): 0 - 45
Temperature range (°C): 27.314 - 28.471
Nitrate (umol/L): 0.054 - 4.021
Salinity (PPS): 34.400 - 35.291
Oxygen (ml/l): 4.467 - 4.608
Phosphate (umol/l): 0.087 - 0.566
Silicate (umol/l): 1.130 - 2.603
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.
Trusted
Conservation
Conservation Status
IUCN Red List Assessment
Red List Category
LC
Least Concern
Red List Criteria
Version
3.1
Year Assessed
2008
Assessor/s
Sheppard, A., Fenner, D., Edwards, A., Abrar, M. & Ochavillo, D.
Reviewer/s
Livingstone, S., Polidoro, B. & Smith, J. (Global Marine Species Assessment)
Contributor/s
Justification
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). This species is widespread and common throughout its range, has a low susceptibility to bleaching, 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 21% 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.
Trusted
Trends
Population
Population
Population Trend
This species is common.
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.
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.
Population Trend
Unknown
Trusted
Threats
Major Threats
Porites species are heavily collected for the aquarium trade. In Indonesia, the catch quota for this genus is 55,500 per year.
The genus is not particularly susceptible to bleaching, but is more prone to disease than many other corals. Coral disease has emerged as a serious threat to coral reefs worldwide and is 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 Great Barrier Reef 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.
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 also 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.
The genus is not particularly susceptible to bleaching, but is more prone to disease than many other corals. Coral disease has emerged as a serious threat to coral reefs worldwide and is 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 Great Barrier Reef 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.
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 also 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.
Trusted
Management
Conservation Actions
Conservation Actions
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.
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.
Trusted

