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 |
---|---|---|
- | - | - |
Year | Category | Criteria |
---|---|---|
2024 | Near Threatened | A3c; C2a(ii) |
2016 | Vulnerable | C1+2a(ii) |
2013 | Vulnerable | A3c+4c;C2a(ii) |
2012 | Vulnerable | A3c+4c;C2a(ii) |
2008 | Vulnerable | A3c; C2a(ii) |
2006 | Vulnerable | |
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 |
Average mass | - |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 228,000 km2 | medium |
Extent of Occurrence (non-breeding) | 301,000 km2 | medium |
Number of locations | 200-500 | - |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 7000-8000 mature individuals | good | estimated | 2023 |
Population trend | stable | good | inferred | - |
Rate of change over the future 10 years/3 generations (longer of the two periods) | 0-29% | - | - | - |
Generation length | 9.6 years | - | - | - |
Number of subpopulations | 1 | - | - | - |
Percentage of mature individuals in largest subpopulation | 100% | - | - | - |
Population justification: Previous population estimates (Manry, 1985, Henderson 2015, Colyn et al. 2020) are the result of extrapolations from the number of breeding adults at monitored colonies; that used in the previous Red List assessment (BirdLife 2016) of 3,300-4,000 mature individuals was based on Henderson (2015). But these estimates are now thought to have underestimated the true population size. The underlying data here is the number of pairs that are breeding at a colony in a particular year, whereas we now know that a large proportion of the mature population do not breed each year and are therefore not available to be counted (Lee et al. in prep.). Conservatively accounting for the missed proportion of individuals by using the single highest count per pentad in the citizen science dataset (SABAP2) and also employing a conservative range estimate Lee et al. (in prep.) propose that the likely minimum global population is 7,000 individuals in the breeding season and 11,000 individuals outside the breeding season, and 10,000 individuals across seasons. The ratio of adults to immatures based on the colony data is between 70-80% (Lee et al. in prep.). Hence the minimum population size is likely to be 7,000-8,000 mature individuals.
There is no evidence for a change in the reporting rate between the two SABAP atlas periods up to 2014 and between 2015 and 2022 the species appears to have been slightly more widely reported (Lee et al. in prep.). Within the reporting period for SABAP2 a dynamic occupancy model showed no linear trend in probabilities of colonisation nor extinction, with probability of colonisation slightly higher than extinction (Lee et al. in prep.). An analysis of species distribution models did show that the probability of the species being recorded in the second SAPAB2 period (2015-2022) was slightly lower than in the first (2007-2014). Colony monitoring indicated little change in overall numbers of nests at monitored sites. 26 of 319 colonies found since 2000 have been abandoned, but new colonies are also being found and two small abandoned sites have since been recolonised (Lee et al. in prep.).
Trend justification: Overall, monitoring data from multiple sources indicates that the species' population has been likely stable over the past few decades (Lee et al. in prep.), suggesting that recorded colony abandonments (Colyn et al. 2020) largely result in the redistribution of breeding adults. The abandonment of colonies may still be a sign that the population will decline (Lee et al. in prep.) and there may be a delay before it is evident at the scale of the analysis conducted. The population impacts of grassland habitat conversion exacerbated by climate change are uncertain but the future projection of an overall contraction in suitable area of habitat equivalent to 29% over three generations, predominately in the north and west of the currently occupied breeding range, and ongoing conversion of grassland habitat suggests that slow to moderately rapid declines may occur in the future (Colyn et al. 2020, Lee et al. in prep).
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
Eswatini | extant | native | yes | |||
Lesotho | extant | native | yes | |||
South Africa | extant | native | yes |
Country/Territory | IBA Name |
---|---|
Eswatini | Mahamba Mountain |
Eswatini | Malolotja Nature Reserve |
Lesotho | Liqobong |
Lesotho | Mafika - Lisiu |
Lesotho | Sehlabathebe National Park |
Lesotho | Sehonghong and Matebeng |
Lesotho | Upper Quthing Valley |
Lesotho | Upper Senqu River |
South Africa | Alexpan |
South Africa | Amersfoort - Bethal - Carolina District |
South Africa | Blyde River Canyon |
South Africa | Chrissie Pans |
South Africa | Golden Gate Highlands National Park |
South Africa | Grasslands |
South Africa | Hlatikulu |
South Africa | Hluhluwe-iMfolozi Park |
South Africa | Impendle Nature Reserve |
South Africa | Ingula Nature Reserve |
South Africa | Ithala Game Reserve |
South Africa | Kaapsehoop |
South Africa | KwaZulu-Natal Mistbelt Grasslands |
South Africa | Maloti Drakensberg Park |
South Africa | Matatiele Nature Reserve |
South Africa | Rooiberge-Riemland |
South Africa | Songimvelo Nature Reserve |
South Africa | Steenkampsberg |
South Africa | Sterkfontein Dam Nature Reserve |
South Africa | Umvoti Vlei |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Artificial/Terrestrial | Arable Land | suitable | non-breeding |
Artificial/Terrestrial | Arable Land | suitable | breeding |
Artificial/Terrestrial | Pastureland | suitable | non-breeding |
Artificial/Terrestrial | Pastureland | suitable | breeding |
Grassland | Subtropical/Tropical High Altitude | major | non-breeding |
Grassland | Subtropical/Tropical High Altitude | major | breeding |
Rocky areas (eg. inland cliffs, mountain peaks) | major | breeding | |
Altitude | 10 - 2900 m | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Agriculture & aquaculture | Annual & perennial non-timber crops - Agro-industry farming | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
|||||||||
Agriculture & aquaculture | Wood & pulp plantations - Agro-industry plantations | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Biological resource use | Hunting & trapping terrestrial animals - Intentional use (species is the target) | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Climate change & severe weather | Habitat shifting & alteration | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Energy production & mining | Mining & quarrying | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Human intrusions & disturbance | Work & other activities | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Pollution | Agricultural & forestry effluents - Herbicides and pesticides | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Unknown | Unknown | ||||||
|
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Residential & commercial development | Housing & urban areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Transportation & service corridors | Utility & service lines | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
Purpose | Scale |
---|---|
Food - human | subsistence, national |
Pets/display animals, horticulture | international |
Recommended citation
BirdLife International (2024) Species factsheet: Southern Bald Ibis Geronticus calvus. Downloaded from
https://datazone.birdlife.org/species/factsheet/southern-bald-ibis-geronticus-calvus 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.