Taxonomic note
Acrocephalus caffer, A. musae and A. longirostris (del Hoyo and Collar 2016) were previously lumped as A. caffer following Sibley and Monroe (1990, 1993).
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 |
---|---|---|
- | - | D1 |
Year | Category | Criteria |
---|---|---|
2020 | Vulnerable | D1 |
2016 | Endangered | B1ab(ii,iii,v);C2a(i) |
2012 | Not Recognised | |
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) | 420 km2 | medium |
Area of Occupancy (breeding/resident) | 456 km2 | |
Number of locations | 19-100 | - |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 250-999 mature individuals | poor | estimated | 2018 |
Population trend | stable | poor | estimated | 1998-2008 |
Generation length | 2.8 years | - | - | - |
Number of subpopulations | 1 | - | - | - |
Percentage of mature individuals in largest subpopulation | 100% | - | - | - |
Population justification: The population was estimated to number a few hundred individuals by Monnet et al. (1993). Surveys in 2017-18 recorded a minimum of 181 breeding territories and estimated at least 372 adults, noting that they were unable to access all valleys where the species was previously recorded (Lazzari et al. 2018, SOP Manu 2019). The population size is placed in the band 250-999 mature individuals.
Trend justification: Surveys have been carried out in 39 valleys during 1986-91 (Monnet et al. 1993) and during 2017-18 (Lazzari et al. 2018, SOP-Manu 2019). The 1986-91 surveys recorded the species in 12 valleys and estimated the population to number a few hundred individuals (Monnet et al. 1993). The 2017-18 surveys detected the species in 19 valleys, including several valleys where the species was previously reported to be absent, and estimated a population size of at least 372 adults (Lazzari et al. 2018, SOP-Manu 2019). Due to access limitations, the 2017-18 survey did not cover one of the valleys previously surveyed, but all resurveyed valleys that were previously occupied were still occupied (SOP-Manu 2019). The 2017-2018 survey appeared to show a territorial expansion, but differences in survey methodologies, including the use of playback in the later survey, mean that the trend is uncertain and is precautionarily hypothesised to be stable (SOP-Manu 2019).
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
French Polynesia | extant | native | yes |
Country/Territory | IBA Name |
---|---|
French Polynesia | Vallée de la Papenoo |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Artificial/Terrestrial | Plantations | suitable | resident |
Forest | Subtropical/Tropical Moist Lowland | major | resident |
Shrubland | Subtropical/Tropical Moist | major | resident |
Altitude | 50 - 700 m | Occasional altitudinal limits | (max) 1700 m |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Biological resource use | Gathering terrestrial plants - Unintentional effects (species is not the target) | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | No decline | Low Impact: 5 | ||||||
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Human intrusions & disturbance | Recreational activities | 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 - Acridotheres tristis | Timing | Scope | Severity | Impact | ||||
Ongoing | Whole (>90%) | No decline | Medium Impact: 6 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Felis catus | 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 - Miconia calvescens | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | No decline | Low Impact: 5 | ||||||
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Pycnonotus cafer | 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 - Rattus rattus | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | No decline | Low Impact: 5 | ||||||
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Wasmannia auropunctata | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | No decline | Low Impact: 4 | ||||||
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Transportation & service corridors | Roads & railroads | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | No decline | Low Impact: 4 | ||||||
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Recommended citation
BirdLife International (2024) Species factsheet: Tahiti Reed-warbler Acrocephalus caffer. Downloaded from
https://datazone.birdlife.org/species/factsheet/tahiti-reed-warbler-acrocephalus-caffer 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.