Taxonomic source(s)
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.
SACC. 2005 and updates. A classification of the bird species of South America. Available at: https://www.museum.lsu.edu/~Remsen/SACCBaseline.htm.
Critically Endangered | Endangered | Vulnerable |
---|---|---|
- | - | C2a(i) |
Year | Category | Criteria |
---|---|---|
2021 | Near Threatened | A3cd; C1+2a(i) |
2016 | Vulnerable | B1ab(i,ii,iii) |
2013 | Vulnerable | B1ab(i,ii,iii,v) |
2012 | Vulnerable | B1ab(i,ii,iii,v) |
2008 | Vulnerable | B1a+b(i,ii,iii,v) |
2004 | Vulnerable | |
2000 | Vulnerable | |
1996 | Vulnerable | |
1994 | Vulnerable | |
1988 | Threatened |
Migratory status | not a migrant | Forest dependency | does not normally occur in forest |
Land-mass type |
continent shelf island |
Average mass | - |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 135,000 km2 | medium |
Area of Occupancy (breeding/resident) | 20,000 km2 | |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 2500-9999 mature individuals | poor | inferred | 2021 |
Population trend | decreasing | poor | inferred | 2000-2025 |
Rate of change over the past 10 years/3 generations (longer of the two periods) | 1-19% | - | - | - |
Rate of change over the future 10 years/3 generations (longer of the two periods) | 1-29% | - | - | - |
Rate of change over the past & future 10 years/3 generations (longer of the two periods) | 1-19% | - | - | - |
Generation length | 8.5 years | - | - | - |
Number of subpopulations | 5 | - | - | - |
Percentage of mature individuals in largest subpopulation | 1-89% | - | - | - |
Population justification: The overall population size is unclear and difficult to assess. The subpopulation on Margarita Island was estimated at 1,600 individuals in 2019 (J. M. Briceño-Linares per Provita in litt. 2020), which equates to roughly 1,000 mature individuals. The subpopulation on Bonaire numbered around 700 individuals in 2017 (DCNA 2018), equating to 450 mature individuals. The most recent estimate from La Blanquilla is from 1996-1998, when the island held around 100 individuals (Sanz and Rodríguez-Ferraro 2006), equating to roughly 60 mature individuals. The subpopulation in north-western Venezuela was estimated at over 5,000 individuals in 2012 (V. Sanz in litt. 2016), equating to roughly 3,300 mature individuals. In view of the ongoing threats, it is suspected that this subpopulation has declined since then (Ferrer-Paris et al. 2014). There are no estimates for the subpopulation in north-eastern Venezuela, but based on observational records (eBird 2021), it is may be smaller than the north-western subpopulation (Ferrer-Paris et al. 2014). Based on the available values for the subpopulation sizes, assuming that the subpopulation in north-western Venezuela is now below 3,300 mature individuals, and accounting for a subpopulation of unknown size in north-eastern Venezuela, it is preliminarily inferred that the total population numbers between 2,500 and 9,999 mature individuals.
The species is assumed to form five subpopulations; on Bonaire, La Blanquilla, Margarita, in north-western Venezuela and north-eastern Venezuela. It is thought that the largest subpopulation is found in north-western Venezuela (C. Sharpe in litt. 2021), which numbered up to 3,300 mature individuals in 2012 but has likely declined since then. It is here tentatively placed in the band 1,000-3,300 mature individuals.
Trend justification: The largest subpopulation on Margarita Island has increased from 750 individuals in 1989 (Sanz and Grajal 1998) to 1,600 individuals in 2019 (J. M. Briceño-Linares per Provita in litt. 2020) and is currently considered to be stable (V. Sanz in litt. 2016). On Bonaire, the size of the subpopulation increased moderately from c. 350 individuals in 1980 to around 700 individuals in 2017 (DCNA 2018). There is no information on the trend of the subpopulation on La Blanquilla. The stable or increasing trends on the islands are due to conservation efforts; if these were to stop the populations may start declining (R. Martin in litt. 2021).
On the mainland, the species was in decline in 2003 (Hilty 2003), but there are no recent trend estimates available. The detection probability was found to be stable in 70% of the mainland range, declining in 18% and increasing in 12% (E. Blanco in litt. 2020). Nevertheless, both subpopulations on the mainland are facing a number of threats, including habitat loss and high pressure from hunting for the bird trade (R. Martin in litt. 2020; Provita in litt. 2020; L. Schmaltz in litt. 2020). It is inferred that as a consequence of these threats, the population on the mainland is undergoing a decline. Despite the stable or increasing trends of the subpopulations on the islands, it is precautionarily assumed that due to the declines on the mainland, the overall population is undergoing a continuing decline. The rate has not been quantified, but is suspected to exceed 10% over three generations (R. Martin and T. James in litt. 2021).
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
Aruba (to Netherlands) | extinct | native | yes | |||
Bonaire, Sint Eustatius and Saba (to Netherlands) | extant | native | yes | |||
Curaçao (to Netherlands) | possibly extant | native | ||||
Venezuela | extant | native | yes |
Country/Territory | IBA Name |
---|---|
Bonaire, Sint Eustatius and Saba (to Netherlands) | Dos Pos, Bonaire |
Bonaire, Sint Eustatius and Saba (to Netherlands) | Lac Bay, Bonaire |
Bonaire, Sint Eustatius and Saba (to Netherlands) | Washikemba - Fontein - Onima, Bonaire |
Bonaire, Sint Eustatius and Saba (to Netherlands) | Washington-Slagbaai National Park, Bonaire |
Venezuela | Humedales Boca de Hueque y Sauca |
Venezuela | Humedales Boca del Río Unare |
Venezuela | Isla La Blanquilla |
Venezuela | Morrocoy National Park |
Venezuela | Parque Nacional El Ávila and surrounding areas |
Venezuela | Parque Nacional Laguna de La Restinga |
Venezuela | Parque Nacional Médanos de Coro |
Venezuela | Parque Nacional Mochima |
Venezuela | Pedernales-Capure |
Venezuela | Refugio de Fauna Silvestre Cuare |
Venezuela | Reserva de Fauna Silvestre Tucurere |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Shrubland | Subtropical/Tropical Dry | major | resident |
Altitude | 0 - 450 m | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Agriculture & aquaculture | Marine & freshwater aquaculture - Industrial aquaculture | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Causing/Could cause fluctuations | Low Impact: 5 | ||||||
|
|||||||||
Biological resource use | Hunting & trapping terrestrial animals - Intentional use (species is the target) | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Rapid Declines | Medium Impact: 7 | ||||||
|
|||||||||
Biological resource use | Hunting & trapping terrestrial animals - Persecution/control | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
|||||||||
Biological resource use | Logging & wood harvesting - Unintentional effects: (subsistence/small scale) [harvest] | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
|||||||||
Energy production & mining | Mining & quarrying | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Causing/Could cause fluctuations | Low Impact: 5 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Capra hircus | 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 - Equus asinus | 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 - Felis catus | 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 - Unspecified species | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Causing/Could cause fluctuations | Low Impact: 5 | ||||||
|
|||||||||
Residential & commercial development | Commercial & industrial areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
|||||||||
Residential & commercial development | Housing & urban areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
|||||||||
Residential & commercial development | Tourism & recreation areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
Purpose | Scale |
---|---|
Pets/display animals, horticulture | national, international |
Recommended citation
BirdLife International (2024) Species factsheet: Yellow-shouldered Amazon Amazona barbadensis. Downloaded from
https://datazone.birdlife.org/species/factsheet/yellow-shouldered-amazon-amazona-barbadensis 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.