Taxonomic note
Previously placed in Sylvia (del Hoyo and Collar 2016) but moved to current genus following Cai et al. (2019). Until recently considered conspecific with C. hortensis following Cramp et al. (1977–1994), Dowsett and Forbes-Watson (1993), and Sibley and Monroe (1990, 1993), but differs in its more clearly demarcated slaty crown and paler mantle and back (2); whiter underparts (1); slightly larger size including longer bill (effect size for bill 2.41, score 2); and different song, involving greater length of phrase (at least 2), number of notes per phrase (ns2), higher maximum number (five vs two) of repetitions of same note (3), and number of different note types per phrase (ns2). Form balchanica of dubious validity, perhaps part of a cline (Svensson 2012). Three subspecies currently recognized.
Taxonomic source(s)
Handbook of the Birds of the World and BirdLife International. 2021. Handbook of the Birds of the World and BirdLife International digital checklist of the birds of the world. Version 6. Available at: https://datazone.birdlife.org/userfiles/file/Species/Taxonomy/HBW-BirdLife_Checklist_v6_Dec21.zip.
Critically Endangered | Endangered | Vulnerable |
---|---|---|
- | - | - |
Year | Category | Criteria |
---|---|---|
2024 | Least Concern | |
2016 | Least Concern | |
2012 | Not Recognised | |
2008 | Not Recognised | |
2004 | Not Recognised | |
2000 | Not Recognised | |
1994 | Not Recognised | |
1988 | Not Recognised |
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) | 10,700,000 km2 | |
Extent of Occurrence (non-breeding) | 11,700,000 km2 | |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 291000-913000 mature individuals | poor | estimated | 2018 |
Population trend | unknown | - | estimated | - |
Generation length | 2.32 years | - | - | - |
Population justification: In Europe, the total population size is estimated at 131,000-411,000 mature individuals, with 65,900-206,000 breeding pairs (BirdLife International 2021), and comprises approximately 45% of the species' global range, so a very preliminary estimate of the global population size is between 291,000-913,000 mature individuals, although further validation of this estimate is desirable. In Europe the trend for this species is not known (BirdLife International 2021). As no other data are available to derive trends, the global population trend for this species is unknown.
Trend justification: .
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
Afghanistan | extant | native | yes | |||
Albania | extant | native | yes | |||
Armenia | extant | native | yes | |||
Austria | extant | vagrant | ||||
Azerbaijan | extant | native | yes | |||
Bahrain | extant | native | yes | |||
Bosnia and Herzegovina | extant | native | yes | |||
Bulgaria | extant | native | yes | |||
Croatia | extant | native | yes | |||
Cyprus | extant | native | yes | |||
Czechia | extant | vagrant | ||||
Egypt | extant | native | ||||
Eritrea | extant | native | ||||
Ethiopia | extant | native | ||||
France | extant | native | yes | |||
Georgia | extant | native | yes | |||
Germany | extant | vagrant | ||||
Greece | extant | native | yes | yes | ||
Iran, Islamic Republic of | extant | native | yes | yes | ||
Iraq | extant | native | yes | yes | ||
Israel | extant | native | yes | |||
Jordan | extant | native | yes | yes | ||
Kazakhstan | extant | native | yes | |||
Kuwait | extant | native | yes | |||
Kyrgyzstan | extant | native | yes | |||
Lebanon | extant | native | yes | yes | ||
Luxembourg | extant | vagrant | ||||
Malta | extant | vagrant | ||||
Montenegro | extant | native | yes | |||
Nepal | extant | vagrant | ||||
North Macedonia | extant | native | yes | |||
Oman | extant | native | yes | yes | ||
Palestine | extant | native | yes | yes | ||
Qatar | extant | native | yes | |||
Saudi Arabia | extant | native | yes | |||
Senegal | extant | native | ||||
Serbia | extant | native | yes | |||
Slovakia | extant | vagrant | ||||
Slovenia | possibly extinct | native | yes | |||
South Sudan | extant | native | yes | |||
Sudan | extant | native | ||||
Syria | extant | native | yes | yes | ||
Tajikistan | extant | native | yes | |||
Türkiye | extant | native | yes | |||
Turkmenistan | extant | native | yes | |||
United Arab Emirates | extant | native | yes | yes | ||
Uzbekistan | extant | native | yes | |||
Yemen | extant | native | yes |
Country/Territory | IBA Name |
---|---|
Armenia | Meghri |
Greece | East Lakonia mountains |
Greece | Filiouri valley and eastern Rodopi mountains |
Greece | Mount Mavrovouni, Larisa |
Greece | Mount Taygetos |
Greece | National Park of Dadia - Lefkimi - Soufli forest |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Artificial/Terrestrial | Plantations | suitable | breeding |
Artificial/Terrestrial | Rural Gardens | suitable | breeding |
Grassland | Subtropical/Tropical Dry | suitable | non-breeding |
Savanna | Dry | suitable | non-breeding |
Shrubland | Mediterranean-type Shrubby Vegetation | major | breeding |
Shrubland | Subtropical/Tropical Dry | suitable | non-breeding |
Shrubland | Subtropical/Tropical Dry | suitable | breeding |
Altitude | 0 - 3000 m | Occasional altitudinal limits |
Purpose | Scale |
---|---|
Sport hunting/specimen collecting | subsistence, national |
Recommended citation
BirdLife International (2024) Species factsheet: Eastern Orphean Warbler Curruca crassirostris. Downloaded from
https://datazone.birdlife.org/species/factsheet/eastern-orphean-warbler-curruca-crassirostris on 22/12/2024.
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 22/12/2024.