Taxonomic source(s)
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 |
---|---|---|
- | C2a(ii) | B1ab(ii,iii,v); C2a(ii); D2 |
Year | Category | Criteria |
---|---|---|
2021 | Endangered | C2a(ii) |
2016 | Critically Endangered | C2a(ii) |
2013 | Critically Endangered | C2a(ii) |
2012 | Critically Endangered | C2a(ii) |
2011 | Critically Endangered | C2a(ii) |
2008 | Not Recognised | |
2004 | Not Recognised | |
2000 | Not Recognised | |
1994 | Not Recognised | |
1988 | Not Recognised |
Migratory status | not a migrant | Forest dependency | medium |
Land-mass type | Average mass | - |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 8,200 km2 | medium |
Number of locations | 1 | - |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 2400-8400 mature individuals | good | estimated | 2021 |
Population trend | decreasing | poor | inferred | - |
Generation length | 3.42 years | - | - | - |
Number of subpopulations | 1 | - | - | - |
Percentage of mature individuals in largest subpopulation | 100% | - | - | - |
Population justification:
Point count surveys following a distance sampling design in northern North Andros estimated a population of c. 1,200-2,800 mature individuals in the study area (Rowley et al. 2021). The study site included the largest area of pine forest on Andros, which was found to be the species’ preferred habitat (Rowley et al. 2021). These forests may represent around 30-50% of good pine forest habitat present on Andros and may hold a large proportion of the global population, as other pine forests are small, patchy and likely not used as much by the species (J. Antalffy and K. Omland pers. comm. 2021). Tentatively, it is assumed that global population is 2-3 times higher than the estimate for the study site in North Andros (J. Antalffy and K. Omland pers. comm. 2021) and is therefore here placed in the band 2,400-8,400 mature individuals.
The species has been extirpated from Abaco and now only occurs on Andros. Its ability to use a variety of habitats suggests that all individuals may get in contact with each other, and it is therefore assumed that the species forms a single subpopulation.
Trend justification: The species is thought to undergo a continuing decline due to the combined effects of predation by invasive species, nest parasitism by Shiny Cowbirds and the loss and degradation of its preferred pine forest habitat through the impacts of hurricanes and subsequent saltwater inundations, as well as through clearance for agriculture.
The rate of decline has not been quantified, but it is considered unlikely to exceeded 30% over the past three generations (10.3 years; Bird et al. 2020). The rate of decline may however increase rapidly in the future, as the species and its habitat are at high risk of hurricanes and storm-surge flooding. The intensity, and probably the frequency of hurricanes in the Atlantic are projected to increase with climate change (see e.g., Knutson et al. 2010; Walsh et al. 2016; Hall and Kossin 2019). While pine forests show resilience to storms, they are very sensitive to flooding and saltwater inundation and may take decades to recover (B. Watson pers. comm. 2021). Potentially severe storms and flooding on Andros in the near future may prove detrimental for the species and its habitat and increase the rate of decline considerably.
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
Bahamas | extant | native | yes |
Country/Territory | IBA Name |
---|---|
Bahamas | Driggs Hill to Mars Bay |
Bahamas | Mangrove Cay |
Bahamas | Owenstown |
Bahamas | Red Bays |
Bahamas | San Andros Pond |
Bahamas | Stafford Creek to Andros Town |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Artificial/Terrestrial | Arable Land | suitable | resident |
Artificial/Terrestrial | Plantations | suitable | resident |
Forest | Subtropical/Tropical Dry | major | resident |
Introduced vegetation | suitable | resident | |
Altitude | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Agriculture & aquaculture | Annual & perennial non-timber crops - Scale Unknown/Unrecorded | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Slow, Significant Declines | Medium Impact: 6 | ||||||
|
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Climate change & severe weather | Habitat shifting & alteration | Timing | Scope | Severity | Impact | ||||
Future | Whole (>90%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Climate change & severe weather | Storms & flooding | Timing | Scope | Severity | Impact | ||||
Past, Likely to Return | Majority (50-90%) | Rapid Declines | Past Impact | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Canis familiaris | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Felis catus | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Causing/Could cause fluctuations | Medium Impact: 6 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Molothrus bonariensis | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Pantherophis guttatus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | No decline | Low Impact: 4 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Procyon lotor | Timing | Scope | Severity | Impact | ||||
Unknown | Minority (<50%) | Negligible declines | Unknown | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Rattus rattus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Unspecified species | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Chilabothrus strigilatus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Cubophis vudii | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Natural system modifications | Fire & fire suppression - Increase in fire frequency/intensity | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Slow, Significant Declines | Medium Impact: 6 | ||||||
|
Recommended citation
BirdLife International (2024) Species factsheet: Bahama Oriole Icterus northropi. Downloaded from
https://datazone.birdlife.org/species/factsheet/bahama-oriole-icterus-northropi on 28/12/2024.
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 28/12/2024.