Taxonomic source(s)
Brooke, M. de L. 2004. Albatrosses and Petrels Across the World. Oxford University Press, Oxford.
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.
Critically Endangered | Endangered | Vulnerable |
---|---|---|
- | - | - |
Year | Category | Criteria |
---|---|---|
2018 | Least Concern | |
2016 | Least Concern | |
2012 | Least Concern | |
2009 | Least Concern | |
2008 | Least Concern | |
2004 | Least Concern | |
2000 | Lower Risk/Least Concern | |
1994 | Lower Risk/Least Concern | |
1988 | Lower Risk/Least Concern |
Migratory status | full migrant | Forest dependency | does not normally occur in forest |
Land-mass type | Average mass | 176 g |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 26,600,000 km2 | |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | unknown | poor | estimated | 2004 |
Population trend | decreasing | - | suspected | - |
Generation length | 15.6 years | - | - | - |
Population justification: Brooke (2004) estimated the global population to approach c.1,000,000 individuals, while the population in Japan has been estimated at c.100-10,000 breeding pairs and c.50-1,000 individuals on migration (Brazil 2009).
Trend justification: The population is suspected to be in decline owing to predation by invasive species.
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
China (mainland) | extant | native | ||||
Japan | extant | native | yes | |||
Marshall Islands | extant | native | yes | |||
Micronesia, Federated States of | extant | uncertain | ||||
Northern Mariana Islands (to USA) | extant | native | yes | |||
Philippines | extant | native | ||||
Russia | extant | native | yes | |||
Russia (Asian) | extant | native | yes | |||
South Korea | extant | uncertain | ||||
Taiwan, China | extant | native | ||||
United States Minor Outlying Islands (to USA) | extant | uncertain | ||||
USA | extant | native | yes |
Country/Territory | IBA Name |
---|---|
USA | Northwestern Hawaiian Islands |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Marine Coastal/Supratidal | Sea Cliffs and Rocky Offshore Islands | major | breeding |
Marine Neritic | Macroalgal/Kelp | suitable | non-breeding |
Marine Neritic | Macroalgal/Kelp | suitable | breeding |
Marine Neritic | Pelagic | major | non-breeding |
Marine Neritic | Pelagic | major | breeding |
Marine Neritic | Seagrass (Submerged) | suitable | non-breeding |
Marine Neritic | Seagrass (Submerged) | suitable | breeding |
Marine Neritic | Subtidal Loose Rock/pebble/gravel | suitable | non-breeding |
Marine Neritic | Subtidal Loose Rock/pebble/gravel | suitable | breeding |
Marine Neritic | Subtidal Rock and Rocky Reefs | suitable | non-breeding |
Marine Neritic | Subtidal Rock and Rocky Reefs | suitable | breeding |
Marine Neritic | Subtidal Sandy | suitable | non-breeding |
Marine Neritic | Subtidal Sandy | suitable | breeding |
Marine Neritic | Subtidal Sandy-Mud | suitable | non-breeding |
Marine Neritic | Subtidal Sandy-Mud | suitable | breeding |
Marine Oceanic | Epipelagic (0-200m) | major | non-breeding |
Marine Oceanic | Epipelagic (0-200m) | major | breeding |
Marine Oceanic | Mesopelagic (200-1000m) | major | non-breeding |
Marine Oceanic | Mesopelagic (200-1000m) | major | breeding |
Altitude | 0 - 918 m | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Climate change & severe weather | Habitat shifting & alteration | Timing | Scope | Severity | Impact | ||||
Future | Majority (50-90%) | Slow, Significant Declines | Low Impact: 4 | ||||||
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Climate change & severe weather | Storms & flooding | Timing | Scope | Severity | Impact | ||||
Future | Minority (<50%) | No/Negligible Impact: 2 | |||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Mus musculus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Unknown | Unknown | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Oryctolagus cuniculus | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Majority (50-90%) | Slow, Significant Declines | Past Impact | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Rattus exulans | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Minority (<50%) | Rapid Declines | Past Impact | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Rattus rattus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
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Recommended citation
BirdLife International (2024) Species factsheet: Bonin Petrel Pterodroma hypoleuca. Downloaded from
https://datazone.birdlife.org/species/factsheet/bonin-petrel-pterodroma-hypoleuca on 22/11/2024.
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 22/11/2024.