Taxonomic source(s)
Brooke, M. de L. 2004. Albatrosses and Petrels Across the World. Oxford University Press, Oxford.
Christidis, L. and Boles, W.E. 2008. Systematics and Taxonomy of Australian Birds. CSIRO Publishing, Collingwood, Australia.
del Hoyo, J., Collar, N.J., Christie, D.A., Elliott, A. and Fishpool, L.D.C. 2014. HBW and BirdLife International Illustrated Checklist of the Birds of the World. Volume 1: Non-passerines. Lynx Edicions BirdLife International, Barcelona, Spain and Cambridge, UK.
Robertson, C. J. R.; Nunn, G. B. 1998. Towards a new taxonomy for albatrosses. In: Robertson, G.; Gales, R. (ed.), Albatross biology and conservation, pp. 13-19. Surrey Beatty & Sons, Chipping Norton, Australia.
SACC. 2005 and updates. A classification of the bird species of South America. Available at: https://www.museum.lsu.edu/~Remsen/SACCBaseline.htm.
Critically Endangered | Endangered | Vulnerable |
---|---|---|
- | A4bd | A4bd; B2ab(v) |
Year | Category | Criteria |
---|---|---|
2018 | Endangered | A4bd |
2016 | Endangered | A4bd |
2012 | Endangered | A4bd |
2010 | Endangered | A4b,d |
2008 | Endangered | A4b,d |
2007 | Endangered | |
2005 | Endangered | |
2004 | Endangered | |
2003 | Endangered | |
2000 | Vulnerable | |
1994 | Lower Risk/Near Threatened | |
1988 | Lower Risk/Least Concern |
Migratory status | full migrant | Forest dependency | does not normally occur in forest |
Land-mass type | Average mass | 2,500 g |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 76,200,000 km2 | medium |
Extent of Occurrence (non-breeding) | 36,200,000 km2 | medium |
Area of Occupancy (breeding/resident) | 1,900 km2 | medium |
Number of locations | 6-10 | - |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 21234-28656 mature individuals | medium | estimated | 1998 |
Population trend | decreasing | medium | suspected | 1980-2070 |
Rate of change over the past & future 10 years/3 generations (longer of the two periods) | 60% | - | - | - |
Generation length | 30 years | - | - | - |
Number of subpopulations | 5 | - | - | - |
Population justification: The population is estimated at 10,617 - 14,328 breeding pairs.
Trend justification: On Possession Island (Crozet), the population declined by 58% between 1980 and 1995 (Weimerskirch and Jouventin 1998) and continues to decline, although at a slower rate (Delord et al. 2008). This equates to an 82% decline between 1980 and 2006 at an average rate of 4.2% per year (Delord et al. 2008). Although since 2006 the population has been increasing again at 2.7% per year, the numbers remain low compared to those of 20 or more years ago. On Marion Island, the population declined by 25% from 1990-1998 (a decline of about 2.6% per year: Crawford et al. 2003) and continued to decline at about 3% per year from 1998 to 2006 (Schoombie et al. 2016). However, from 2006 to 2014, the population has increased at c. 4% per year (Schoombie et al. 2016). On Gough Island (c.36% global population), the population appears to have decreased by over 50% from 1972-2000 (Cuthbert and Sommer 2004a), although recent counts of breeding birds indicates the number of breeding pairs remained stable from 2000 and 2015 (Cuthbert et al. 2014). Limited counts have been made on Tristan and Inaccessible, and indicate a population of c.3,157 (ACAP 2012). Overall, these declines equate to 60% over three generations (90 years), with a trend start date of 1960. However, this species, being a biennial breeder, has a highly variable breeding population between years. Better data are required from Gough and Prince Edward Islands, in particular whether the population on Prince Edward is increasing. The long life expectancy of the species makes it difficult to determine the period over which an analysis of trends should be conducted.
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
Antarctica | extant | vagrant | ||||
Argentina | extant | native | yes | |||
Australia | extant | native | yes | |||
Brazil | extant | native | yes | |||
Falkland Islands (Malvinas) | extant | vagrant | ||||
French Southern Territories | extant | native | yes | |||
Heard Island and McDonald Islands (to Australia) | extant | native | yes | |||
High Seas | extant | native | yes | |||
Mauritius | extant | vagrant | ||||
New Zealand | extant | vagrant | ||||
Réunion (to France) | extant | vagrant | ||||
South Africa | extant | native | yes | |||
South Georgia & the South Sandwich Islands | extant | vagrant | ||||
St Helena (to UK) | extant | native | yes | |||
Uruguay | extant | native | yes |
Country/Territory | IBA Name |
---|---|
French Southern Territories | Falaises d'Entrecasteaux |
French Southern Territories | Île aux Cochons |
French Southern Territories | Île de l'Est |
French Southern Territories | Île de la Possession |
French Southern Territories | Île des Pingouins |
French Southern Territories | Île Saint Paul |
French Southern Territories | Îles des Apôtres |
High Seas | Atlantic, Southeast 14 - Marine |
High Seas | Indian Ocean, Antarctic and Southern 15 - Marine |
High Seas | Indian Ocean, Western 1 - Marine |
South Africa | Prince Edward Islands Special Nature Reserve |
St Helena (to UK) | Gough Island |
St Helena (to UK) | Inaccessible Island |
St Helena (to UK) | Nightingale Island group |
St Helena (to UK) | Tristan Island |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Marine Coastal/Supratidal | Sea Cliffs and Rocky Offshore Islands | major | breeding |
Marine Neritic | Pelagic | major | non-breeding |
Marine Neritic | Pelagic | major | breeding |
Marine Oceanic | Epipelagic (0-200m) | major | non-breeding |
Marine Oceanic | Epipelagic (0-200m) | major | breeding |
Altitude | 0 - 500 m | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Biological resource use | Fishing & harvesting aquatic resources - Unintentional effects: (large scale) [harvest] | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Slow, Significant Declines | Medium Impact: 6 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Erysipelothrix rhusiopathiae | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Felis catus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Mus musculus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Pasteurella multocida | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Rattus rattus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Unknown | Unknown | ||||||
|
Purpose | Scale |
---|---|
Food - human | subsistence, national |
Recommended citation
BirdLife International (2024) Species factsheet: Sooty Albatross Phoebetria fusca. Downloaded from
https://datazone.birdlife.org/species/factsheet/sooty-albatross-phoebetria-fusca on 25/11/2024.
Recommended citation for factsheets for more than one species: BirdLife International (2024) IUCN Red List for birds. Downloaded from
https://datazone.birdlife.org/species/search on 25/11/2024.