Status_ne_offStatus_dd_offStatus_lc_offStatus_nt_offStatus_vu_onStatus_en_offStatus_cr_offStatus_ew_offStatus_ex_off

Taxonomy [top]

Kingdom Phylum Class Order Family
Animalia Cnidaria Anthozoa Scleractinia Poritidae

Scientific Name: Alveopora marionensis
Species Authority: Veron & Pichon, 1982

Assessment Information [top]

Red List Category & Criteria: Vulnerable A4c ver 3.1
Year Published: 2008
Date Assessed: 2008-01-01
Assessor(s): Sheppard, A., Fenner, D., Edwards, A., Abrar, M. & Ochavillo, D.
Reviewer(s): Livingstone, S., Polidoro, B. & Smith, J. (Global Marine Species Assessment)
Justification:
This species is widespread, and is rare throughout its range. However, it is particularly susceptible to bleaching, harvesting for aquarium trade, 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 36% over three generation lengths (30 years) is the best inference of population reduction and meets the threshold for Vulnerable under Criterion A4c. It will be important to reassess this species in 10 years time because of predicted threats from climate change and ocean acidification.

Geographic Range [top]

Range Description:This species is found in the central Indo-Pacific, South-east Asia, eastern Australia, and oceanic West Pacific.
Countries occurrence:
Native:
Australia; Cambodia; Fiji; Indonesia; Kiribati; Malaysia; Marshall Islands; Micronesia, Federated States of ; Nauru; New Caledonia; Palau; Papua New Guinea; Philippines; Singapore; Solomon Islands; Taiwan, Province of China; Thailand; Tuvalu; Vanuatu; Viet Nam
FAO Marine Fishing Areas:
Native:
Indian Ocean – eastern; Pacific – northwest; Pacific – southwest; Pacific – western central
Lower depth limit (metres):30
Upper depth limit (metres):1
Range Map:Click here to open the map viewer and explore range.

Population [top]

Population:This species is 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 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. See the supplementary material for further details on population decline and generation length estimates.
For further information about this species, see Corals_SupportingDoc.pdf.
A PDF viewer such as Adobe Reader is required.
Current Population Trend:Unknown
Additional data:
Population severely fragmented:No

Habitat and Ecology [top]

Habitat and Ecology:This species is only found in environments with moderate wave action, generally to depths of 30 m.
Systems:Marine
Generation Length (years):10

Threats [top]

Major Threat(s): Species of this genus are attractive to the aquarium trade due to their physical appearance. Threats to this species therefore include coral removal and harvesting for display in aquariums and for the curio-trade. In addition, the Alveopora genus was ranked as having the highest bleaching response and is in the top ten genera for extinction risk in the Western Indian Ocean (McClanahan et al. 2007). However, Alveopora species are considered to be relatively insusceptible to disease.

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.

Conservation Actions [top]

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.

Classifications [top]

9. Marine Neritic -> 9.2. Marine Neritic - Subtidal Rock and Rocky Reefs
suitability: Suitable  
9. Marine Neritic -> 9.8. Marine Neritic - Coral Reef -> 9.8.1. Outer Reef Channel
suitability: Suitable  
9. Marine Neritic -> 9.8. Marine Neritic - Coral Reef -> 9.8.2. Back Slope
suitability: Suitable  
9. Marine Neritic -> 9.8. Marine Neritic - Coral Reef -> 9.8.3. Foreslope (Outer Reef Slope)
suitability: Suitable  
9. Marine Neritic -> 9.8. Marine Neritic - Coral Reef -> 9.8.4. Lagoon
suitability: Suitable  
9. Marine Neritic -> 9.8. Marine Neritic - Coral Reef -> 9.8.5. Inter-Reef Soft Substrate
suitability: Unknown  
9. Marine Neritic -> 9.8. Marine Neritic - Coral Reef -> 9.8.6. Inter-Reef Rubble Substrate
suitability: Unknown  
1. Land/water protection -> 1.1. Site/area protection
2. Land/water management -> 2.1. Site/area management
2. Land/water management -> 2.3. Habitat & natural process restoration
3. Species management -> 3.2. Species recovery
3. Species management -> 3.4. Ex-situ conservation -> 3.4.1. Captive breeding/artificial propagation
3. Species management -> 3.4. Ex-situ conservation -> 3.4.2. Genome resource bank

In-Place Research, Monitoring and Planning
In-Place Land/Water Protection and Management
  Occur in at least one PA:Yes
In-Place Species Management
In-Place Education
1. Residential & commercial development -> 1.1. Housing & urban areas
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.1. Ecosystem conversion
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

1. Residential & commercial development -> 1.2. Commercial & industrial areas
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.1. Ecosystem conversion
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

1. Residential & commercial development -> 1.3. Tourism & recreation areas
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.1. Ecosystem conversion
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

4. Transportation & service corridors -> 4.3. Shipping lanes
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

5. Biological resource use -> 5.4. Fishing & harvesting aquatic resources -> 5.4.1. Intentional use: (subsistence/small scale)
♦ timing: Ongoing    
→ Stresses
  • 2. Species Stresses -> 2.1. Species mortality

5. Biological resource use -> 5.4. Fishing & harvesting aquatic resources -> 5.4.3. Unintentional effects: (subsistence/small scale)
♦ timing: Ongoing    
→ Stresses
  • 2. Species Stresses -> 2.1. Species mortality

5. Biological resource use -> 5.4. Fishing & harvesting aquatic resources -> 5.4.6. Motivation Unknown/Unrecorded
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

6. Human intrusions & disturbance -> 6.1. Recreational activities
♦ timing: Ongoing    
→ Stresses
  • 2. Species Stresses -> 2.2. Species disturbance

8. Invasive & other problematic species & genes -> 8.1. Invasive non-native/alien species -> 8.1.1. Unspecified species
♦ timing: Ongoing    
→ Stresses
  • 2. Species Stresses -> 2.1. Species mortality
  • 2. Species Stresses -> 2.2. Species disturbance
  • 2. Species Stresses -> 2.3. Indirect species effects -> 2.3.2. Competition

9. Pollution -> 9.1. Domestic & urban waste water -> 9.1.3. Type Unknown/Unrecorded
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

9. Pollution -> 9.2. Industrial & military effluents -> 9.2.3. Type Unknown/Unrecorded
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

9. Pollution -> 9.3. Agricultural & forestry effluents -> 9.3.2. Soil erosion, sedimentation
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

9. Pollution -> 9.3. Agricultural & forestry effluents -> 9.3.4. Type Unknown/Unrecorded
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

9. Pollution -> 9.5. Air-borne pollutants -> 9.5.3. Ozone
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

11. Climate change & severe weather -> 11.3. Temperature extremes
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation
  • 2. Species Stresses -> 2.1. Species mortality
  • 2. Species Stresses -> 2.2. Species disturbance
  • 2. Species Stresses -> 2.3. Indirect species effects -> 2.3.8. Other

11. Climate change & severe weather -> 11.4. Storms & flooding
♦ timing: Ongoing    
→ Stresses
  • 1. Ecosystem stresses -> 1.2. Ecosystem degradation

1. Research -> 1.1. Taxonomy
1. Research -> 1.2. Population size, distribution & trends
1. Research -> 1.3. Life history & ecology
1. Research -> 1.5. Threats
1. Research -> 1.6. Actions
3. Monitoring -> 3.1. Population trends

♦  Pets/display animals, horticulture
 International : ✓ 

Bibliography [top]

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. 2001b. White-band disease and the changing face of Caribbean coral reefs. Hydrobiologia 460: 25-38.

Bruno, J.F., Selig, E.R., Casey, K.S., Page, C.A., Willis, B.L., Harvell, C.D., Sweatman, H., and Melendy, A.M. 2007. Thermal stress and coral cover as drivers of coral disease outbreaks. PLoS Biology 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.

MaClanahan, T.R., Atteweberhan, M., Graham, N.A.J., Wilson, S.K., Ruiz Sebastian, C., Guillaume, M.M.M., Bruggeman, J.H. 2007. Western Indian Ocean coral communities: bleaching responses and susceptibility to extinction. Marine Ecology Progress Series 337: 1-13.

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, M.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. 2000. Corals of the World. Australian Institute of Marine Science, Townsville.

Wallace, C.C. 1999. Staghorn Corals of the World: a revision 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 Dinsdale, E. 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.


Citation: Sheppard, A., Fenner, D., Edwards, A., Abrar, M. & Ochavillo, D. 2008. Alveopora marionensis. In: The IUCN Red List of Threatened Species 2008: e.T132896A3482552. . Downloaded on 29 June 2016.
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