Taxonomic note
Falco araeus (del Hoyo and Collar 2014) was previously listed as F. araea.
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.
Critically Endangered | Endangered | Vulnerable |
---|---|---|
- | - | D1 |
Year | Category | Criteria |
---|---|---|
2023 | Vulnerable | D1 |
2016 | Vulnerable | B1ab(iii,v);C2a(i);D1 |
2013 | Vulnerable | B1ab(iii,v);C2a(i);D1 |
2012 | Vulnerable | B1ab(iii,v);C2a(i);D1 |
2008 | Vulnerable | C2a(i); D1 |
2006 | Vulnerable | |
2004 | Vulnerable | |
2000 | Vulnerable | |
1996 | Vulnerable | |
1994 | Vulnerable | |
1988 | Lower Risk/Least Concern |
Migratory status | not a migrant | Forest dependency | medium |
Land-mass type | Average mass | - |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 2,080 km2 | medium |
Area of Occupancy (breeding/resident) | 460 km2 | medium |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 700-900 mature individuals | medium | estimated | 2008 |
Population trend | stable | medium | suspected | - |
Generation length | 3.32 years | - | - | - |
Number of subpopulations | 4 | - | - | - |
Percentage of mature individuals in largest subpopulation | 90-94% | - | - | - |
Population justification: Genetic analysis suggests that the global population underwent a crash some time between 1940 and the early 1970s, and at one time numbered as few as eight (3.5-22) individuals, which is compatible with claims that there were fewer than 30 birds on Mahé during the 1960s (Groombridge et al. 2009). The last comprehensive census of this species' population took place between 1975-1977, with the population size then estimated at 430 pairs (Rocamora 2013), which equates to 860 mature individuals. This was mainly split between Mahé and Silhouette (and their respective satellite islands), whose population sizes were estimated at between 380-385 pairs and 35-45 pairs, respectively, and a successfully reintroduced population of 13 individuals on Praslin in 1977.
Since then, populations on various islands have been surveyed, with varying results. Notably, the population on Praslin decreased from ten pairs in the 1980s to six pairs in 2003 (Pandolfi and Barilari 2009); whereas on other islands, populations have either not shown a marked change in size, or not been accurately determined since the last census. In 2013, a total population of at least 530 mature individuals was deduced, using a combination of survey results and records (S. Parr in litt. 1999), however this is now shown to be an error in converting 800 mature individuals down using a 2:3 ratio. All other evidence shows the population still being estimated at close to the numbers from the 1970s (e.g., Rocamora 2013), with an estimation from 2008 of 350 pairs in total (Pandolfi and Barilari 2009), including around 300 pairs on Mahé and another 40-50 pairs on Silhouette. Considering the slightly contradictory nature of these sources, the species' population size is therefore cautiously estimated at between 700 and 900 mature individuals (350 to over 400 pairs).
Trend justification: Following surveys in 2002, the Mahé population was considered stable (Millett et al. 2003). Considerable development and habitat alteration have taken place on Mahé since 2002, and it has been suggested that the population on this island has been impacted by this extensive urbanisation and is therefore unlikely to have increased since then (N. Doak in litt. 2007). However, population declines on this island have not been demonstrated, or linked to this factor.
The Praslin population has declined from around 20 pairs in the 1980s to just a few pairs in the 1990s, and six pairs in 2003 (Rocamora 1997, Pandolfi and Barilari 2009). In addition, a reduction in tree cavities on Praslin since 2003 is likely to have occurred, due to death of Sangdragon trees (Pterocarpus indicus) on the island (Rocamora 2013), inferring, combined with the housing development on Mahé and the spread of non-native predators, a reduction in habitat quality.
Although the overall population was previously inferred to have declined since the 1970s due to a smaller total population size being estimated, as this error in the quantification of the population size has now been rectified, there is no data showing such a reduction since the 1970s, despite the decline on Praslin. It is therefore suspected that the species' population is stable.
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
Seychelles | extant | native | yes |
Country/Territory | IBA Name |
---|---|
Seychelles | Conception island |
Seychelles | Mahé highlands and surrounding areas |
Seychelles | Montagne Glacis - When She Comes |
Seychelles | Praslin National Park and surrounding areas |
Seychelles | Silhouette National Park |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Artificial/Terrestrial | Arable Land | suitable | resident |
Artificial/Terrestrial | Plantations | major | resident |
Artificial/Terrestrial | Urban Areas | suitable | resident |
Forest | Subtropical/Tropical Moist Lowland | major | resident |
Forest | Subtropical/Tropical Moist Montane | major | resident |
Altitude | 0 - 700 m | 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 | ||||
Past, Likely to Return | Minority (<50%) | Slow, Significant Declines | Past Impact | ||||||
|
|||||||||
Biological resource use | Hunting & trapping terrestrial animals - Persecution/control | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Majority (50-90%) | Rapid Declines | Past Impact | ||||||
|
|||||||||
Biological resource use | Logging & wood harvesting - Unintentional effects: (subsistence/small scale) [harvest] | Timing | Scope | Severity | Impact | ||||
Past, Likely to Return | Minority (<50%) | Slow, Significant Declines | Past Impact | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Acridotheres tristis | 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 - Felis catus | 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 - Rattus rattus | 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 - Tyto alba | 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 - Unspecified species | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Causing/Could cause fluctuations | Medium Impact: 6 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Butorides striata | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Negligible declines | Low Impact: 5 | ||||||
|
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Natural system modifications | Fire & fire suppression - Increase in fire frequency/intensity | Timing | Scope | Severity | Impact | ||||
Past, Likely to Return | Minority (<50%) | Negligible declines | Past Impact | ||||||
|
|||||||||
Pollution | Agricultural & forestry effluents - Herbicides and pesticides | Timing | Scope | Severity | Impact | ||||
Future | Majority (50-90%) | Slow, Significant Declines | Low Impact: 4 | ||||||
|
|||||||||
Residential & commercial development | Housing & urban areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Causing/Could cause fluctuations | Low Impact: 5 | ||||||
|
Purpose | Scale |
---|---|
Pets/display animals, horticulture | international |
Recommended citation
BirdLife International (2024) Species factsheet: Seychelles Kestrel Falco araeus. Downloaded from
https://datazone.birdlife.org/species/factsheet/seychelles-kestrel-falco-araeus on 24/12/2024.
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 24/12/2024.