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 |
---|---|---|
- | B1ab(iii)+2ab(iii) | B1ab(iii)+2ab(iii); D1+2 |
Year | Category | Criteria |
---|---|---|
2023 | Endangered | B1ab(iii)+2ab(iii) |
2016 | Critically Endangered | B1ac(iv) |
2015 | Critically Endangered | B1ac(iv) |
2012 | Critically Endangered | B1ac(iv) |
2010 | Critically Endangered | B1a+c(iv) |
2009 | Critically Endangered | B1a+c(iv) |
2008 | Critically Endangered | |
2004 | Critically Endangered | |
2000 | Critically Endangered | |
1996 | Vulnerable | |
1994 | Vulnerable | |
1988 | Threatened |
Migratory status | not a migrant | Forest dependency | does not normally occur in forest |
Land-mass type | Average mass | 18 g |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 2,100 km2 | medium |
Area of Occupancy (breeding/resident) | 24 km2 | |
Number of locations | 2 | - |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 250-999 mature individuals | good | estimated | 2016 |
Population trend | unknown | medium | - | 2000-2010 |
Generation length | 2.99 years | - | - | - |
Number of subpopulations | 2 | - | - | - |
Percentage of mature individuals in largest subpopulation | 1-89% | - | - | - |
Population justification: The naturally occurring population on Nihoa was estimated at 489 ± 70 (SD) in 2010, 699 ± 78 in 2011, 610 ± 210 in 2012, 468 ± 166 in 2013, and 893 ± 303 in 2014 (Gorresen et al. 2016). The most recent estimate of the population on Laysan was 164 in September 2014 (Dalton et al. 2014, Freifeld et al. 2016). Given that the Nihoa subpopulation is thought to fluctuate widely, the population is tentatively placed in the band 250-999 mature individuals. This estimate equates to 375-1,499 individuals in total, rounded here to 350-1,500 individuals.
Trend justification: Although there is a lack of precision over the monitoring methods, the existing data suggest that Millerbird numbers on Nihoa have experienced pronounced fluctuations and have likely ranged between fewer than 50 and more than 800 individuals (VanderWerf et al. 2011). Although it is still thought to undergo substantial fluctuations, the species may not currently be as at risk as in the late 1980s (Gorresen et al. 2016). Numbers on Laysan have greatly increased since translocations in 2011 and 2012 (C. Farmer in litt. 2022). In 2016, population trends were considered inconclusive on Nihoa due to high within-year variance (Gorresen et al. 2016). Although an updated population estimate is not currently available (C. Farmer in litt. 2022), raw detections per effort on Nihoa in 2010-2021 are not indicative of a decline overall (Plentovich et al. 2021). However, detections were reportedly very low in 2022 (R. Rounds in litt. 2022). This may be due to several different reasons including the time of year, however severe drought driven by climate change may be a contributing factor (R. Rounds in litt. 2022, S. Plentovich in litt. 2022). It is currently unclear whether this is a natural fluctuation or if dry conditions from 2022 are indicative of longer-term trends (J. Vetter in litt. 2022), and as such, the population trend is precautionarily considered to be unknown overall.
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
USA | extant | native | yes |
Country/Territory | IBA Name |
---|---|
USA | Northwestern Hawaiian Islands |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Shrubland | Subtropical/Tropical Moist | major | resident |
Altitude | 0 - 270 m | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Climate change & severe weather | Droughts | Timing | Scope | Severity | Impact | ||||
Ongoing | Whole (>90%) | Causing/Could cause fluctuations | Medium Impact: 7 | ||||||
|
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Climate change & severe weather | Habitat shifting & alteration | Timing | Scope | Severity | Impact | ||||
Future | Whole (>90%) | Unknown | Unknown | ||||||
|
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Climate change & severe weather | Storms & flooding | Timing | Scope | Severity | Impact | ||||
Future | Whole (>90%) | Rapid Declines | Medium Impact: 6 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Anoplolepis gracilipes | Timing | Scope | Severity | Impact | ||||
Future | Minority (<50%) | Unknown | Unknown | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Cenchrus echinatus | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Unknown | Unknown | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Named species | Timing | Scope | Severity | Impact | ||||
Future | Whole (>90%) | Rapid Declines | Medium Impact: 6 | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Oryctolagus cuniculus | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Whole (>90%) | Rapid Declines | Past Impact | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Schistocerca nitens | 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 - Unspecified species | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Unknown | Unknown | ||||||
|
|||||||||
Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Telespiza cantans | 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 - Telespiza ultima | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Invasive and other problematic species, genes & diseases | Problematic species/disease of unknown origin - Unspecified species | Timing | Scope | Severity | Impact | ||||
Future | Majority (50-90%) | Rapid Declines | Low Impact: 5 | ||||||
|
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Natural system modifications | Fire & fire suppression - Trend Unknown/Unrecorded | Timing | Scope | Severity | Impact | ||||
Past, Likely to Return | Majority (50-90%) | Rapid Declines | Past Impact | ||||||
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Recommended citation
BirdLife International (2024) Species factsheet: Millerbird Acrocephalus familiaris. Downloaded from
https://datazone.birdlife.org/species/factsheet/millerbird-acrocephalus-familiaris 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.