Data Zone
Taxonomic note
Hydrobates monorhis (del Hoyo and Collar 2014) was previously placed in the genus Oceanodroma.
Taxonomic source(s)
AERC TAC. 2003. AERC TAC Checklist of bird taxa occurring in Western Palearctic region, 15th Draft. Available at: http://www.aerc.eu/DOCS/Bird_taxa_of_the_WP15.xls.
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.
Cramp, S. and Simmons, K.E.L. (eds). 1977-1994. Handbook of the birds of Europe, the Middle East and Africa. The birds of the western Palearctic. 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 | Near Threatened | A3ce |
| 2016 | Near Threatened | A3ce |
| 2013 | Near Threatened | A3ce |
| 2012 | Near Threatened | A3ce |
| 2009 | Least Concern | |
| 2008 | Least Concern | |
| 2004 | Least Concern | |
| 2000 | Lower Risk/Least Concern | |
| 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 | - |
| Estimate | Data quality | |
|---|---|---|
| Extent of Occurrence (breeding/resident) | 36,000,000 km2 | |
| Severely fragmented? | no | - |
| Estimate | Data quality | Derivation | Year of estimate | |
|---|---|---|---|---|
| Population size | 65000 - 260000 mature individuals | poor | estimated | 2010 |
| Population trend | stable | - | suspected | - |
| Rate of change over the future 10 years/3 generations (longer of the two periods) | 20-29% | - | - | - |
| Generation length | 14.6 years | - | - | - |
Population justification: Brooke (2004) estimated the global population to number c.100,000 individuals, which roughly equates to 66,666 mature individuals. Based on Boersma and Groom (1993) and Birdlife International (2009) estimates, Sato et al. (2010) describes the world population at a minimum of 130,000 pairs, which equates to 260,000 mature individuals. The population is therefore estimated at 66,666 - 260,000 mature individuals, rounded here to 65,000 - 260,000 mature individuals.
Trend justification: The population is expected to undergo a moderately rapid decline over the next three generations, owing primarily to the impact of introduced species.
| Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
|---|---|---|---|---|---|---|
| Bangladesh | extant | uncertain | ||||
| Cambodia | extant | uncertain | ||||
| China (mainland) | extant | native | yes | |||
| Christmas Island (to Australia) | extant | uncertain | ||||
| India | extant | uncertain | ||||
| Indonesia | extant | native | ||||
| Israel | extant | vagrant | ||||
| Japan | extant | native | yes | |||
| Malaysia | extant | native | ||||
| Maldives | extant | uncertain | ||||
| Myanmar | extant | uncertain | ||||
| North Korea | extant | native | yes | |||
| Oman | extant | vagrant | yes | |||
| Pakistan | extant | uncertain | ||||
| Philippines | extant | uncertain | ||||
| Portugal | extant | vagrant | ||||
| Russia | extant | native | yes | |||
| Russia (Asian) | extant | native | yes | |||
| Seychelles | extant | vagrant | ||||
| Singapore | extant | native | yes | |||
| Somalia | extant | uncertain | ||||
| South Korea | extant | native | yes | |||
| Spain | extant | vagrant | ||||
| Sri Lanka | extant | native | ||||
| Taiwan, China | extant | native | yes | |||
| Thailand | extant | native | ||||
| United Arab Emirates | extant | native | yes | |||
| United Kingdom | extant | vagrant | ||||
| Vietnam | extant | uncertain | ||||
| Yemen | extant | vagrant | yes |
| Country/Territory | IBA Name |
|---|---|
| Japan | Kanmurijima and Kutsujima islets |
| Japan | Kanmurijima and Kutsujima islets - Marine |
| Russia (Asian) | Islands in Peter the Great bay |
| South Korea | Chilbal-do island |
| South Korea | Kukul-do island |
| 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 | Occasional altitudinal limits |
| Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Energy production & mining | Mining & quarrying | 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 - Artemisia vulgaris | Timing | Scope | Severity | Impact | ||||
| Ongoing | Majority (50-90%) | Negligible declines | Low Impact: 5 | ||||||
|
|||||||||
| Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Rattus norvegicus | Timing | Scope | Severity | Impact | ||||
| Ongoing | Minority (<50%) | Very Rapid Declines | Medium Impact: 7 | ||||||
|
|||||||||
| Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Unspecified species | Timing | Scope | Severity | Impact | ||||
| Ongoing | Majority (50-90%) | Slow, Significant Declines | Medium Impact: 6 | ||||||
|
|||||||||
| Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Calonectris leucomelas | Timing | Scope | Severity | Impact | ||||
| Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
|||||||||
| Pollution | Industrial & military effluents - Type Unknown/Unrecorded | Timing | Scope | Severity | Impact | ||||
| Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
|||||||||
| Residential & commercial development | Tourism & recreation areas | Timing | Scope | Severity | Impact | ||||
| Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Recommended citation
BirdLife International (2024) Species factsheet: Swinhoe's Storm-petrel Hydrobates monorhis. Downloaded from
https://datazone.birdlife.org/species/factsheet/swinhoes-storm-petrel-hydrobates-monorhis on 23/11/2024.
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 23/11/2024.