Data Zone
Taxonomic note
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#.
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#.
Cramp, S. and Perrins, C.M. 1977-1994. Handbook of the birds of Europe, the Middle East and Africa. The birds of the western Palearctic. Oxford University Press, Oxford.
Cramp, S.; Perrins, C. M. 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., Fishpool, L.D.C., Boesman, P. and Kirwan, G.M. 2016. HBW and BirdLife International Illustrated Checklist of the Birds of the World. Volume 2: Passerines. Lynx Edicions and BirdLife International, Barcelona, Spain and Cambridge, UK.
| Critically Endangered | Endangered | Vulnerable |
|---|---|---|
| - | - | - |
| Year | Category | Criteria |
|---|---|---|
| 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 | High |
| Land mass type | Average mass | - |
| Estimate | Data quality | |
|---|---|---|
| Extent of Occurrence breeding/resident (km2) | 6,690,000 | |
| Extent of Occurrence non-breeding (km2) | 10,800,000 | |
| Number of locations | - | |
| Fragmentation | - |
| Estimate | Data quality | Derivation | Year of estimate | |
|---|---|---|---|---|
| No. of mature individuals | unknown | not applicable | not applicable | 0 |
| Population trend | Unknown | not applicable | - | |
| Decline (3 years/1 generation past) | - | - | - | |
| Decline (5 years/1 generation past) | - | - | - | |
| Decline (10 years/1 generation past) | - | - | - | |
| Decline (10 years/3 generation future) | - | - | - | |
| Decline (10 years/3 generation past and future) | - | - | - | |
| Number of subpopulations | - | - | - | |
| Largest subpopulations | - | - | - | |
| Generation length (yrs) | 6.1 | - | - | - |
Population justification: The global population size has not been quantified, but the species is described as fairly common to common throughout most of its range (del Hoyo et al. 2005), while national population estimates include: c.10,000-100,000 breeding pairs and c.50-10,000 individuals on migration in China; c.1,000-10,000 individuals on migration and c.1,000-10,000 wintering individuals in Taiwan; c.50-10,000 individuals on migration and c.50-1,000 wintering individuals in Japan and c.10,000-100,000 breeding pairs and c.1,000-10,000 individuals on migration in Russia (Brazil 2009).
Trend justification: The population trend is difficult to determine because of uncertainty over the impacts of habitat modification on population sizes.
| Country/Territory | Occurrence status | Presence | Resident | Breeding | Non-breeding | Passage |
|---|---|---|---|---|---|---|
| Bangladesh | N | Extant | ||||
| Belgium | V | Extant | ||||
| Bhutan | N | Extant | ||||
| Brunei | N | Extant | ||||
| Cambodia | N | Extant | ||||
| China (mainland) | N | Extant | ||||
| Cyprus | V | Extant | ||||
| Czechia | V | Extant | ||||
| Finland | V | Extant | ||||
| France | V | Extant | ||||
| Germany | V | Extant | ||||
| Hong Kong (China) | N | Extant | ||||
| Hungary | V | Extant | ||||
| India | N | Extant | ||||
| Indonesia | N | Extant | ||||
| Italy | V | Extant | ||||
| Japan | N | Extant | ||||
| Laos | N | Extant | ||||
| Malaysia | N | Extant | ||||
| Maldives | V | Extant | ||||
| Malta | V | Extant | ||||
| Mongolia | N | Extant | Yes | |||
| Myanmar | N | Extant | ||||
| Nepal | V | Extant | ||||
| Netherlands | V | Extant | ||||
| North Korea | N | Extant | ||||
| Norway | V | Extant | ||||
| Oman | V | Extant | Yes | |||
| Palau | V | Extant | ||||
| Philippines | N | Extant | ||||
| Poland | V | Extant | ||||
| Portugal | V | Extant | ||||
| Russia | N | Extant | Yes | |||
| Russia (Asian) | N | Extant | ||||
| Russia (Central Asian) | N | Extant | Yes | |||
| Singapore | N | Extant | ||||
| South Korea | N | Extant | ||||
| Sri Lanka | N | Extant | ||||
| Sweden | V | Extant | ||||
| Taiwan, China | N | Extant | ||||
| Thailand | N | Extant | ||||
| United Arab Emirates | V | Extant | Yes | |||
| United Kingdom | V | Extant | ||||
| USA | V | Extant | Yes | |||
| Vietnam | N | Extant |
| Country/Territory | IBA Name |
|---|
| Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
|---|---|---|---|
| Artificial/Terrestrial | Plantations | suitable | non-breeding |
| Forest | Boreal | major | breeding |
| Forest | Subtropical/Tropical Mangrove Vegetation Above High Tide Level | suitable | non-breeding |
| Forest | Subtropical/Tropical Moist Lowland | suitable | non-breeding |
| Forest | Subtropical/Tropical Moist Montane | suitable | non-breeding |
| Forest | Temperate | suitable | breeding |
| Shrubland | Subtropical/Tropical High Altitude | suitable | non-breeding |
| Shrubland | Subtropical/Tropical Moist | suitable | non-breeding |
| Altitude | 0 - 1500 m | Occasional altitudinal limits | (max) 2400 m |
| Purpose | Primary form used | Life stage used | Source | Scale | Level | Timing |
|---|---|---|---|---|---|---|
| Food - human | - | - | - | Non-trivial | Recent | |
| Pets/display animals, horticulture | - | - | - | Non-trivial | Recent |
Recommended citation
BirdLife International (2020) Species factsheet: Turdus obscurus. Downloaded from
http://www.birdlife.org on 28/02/2020.
Recommended citation for factsheets for more than one species: BirdLife International (2020) IUCN Red List for birds. Downloaded from
http://www.birdlife.org on 28/02/2020.
