VU
Swierstra's Spurfowl Pternistis swierstrai



Taxonomy

Taxonomic note
Pternistis swierstrai (del Hoyo and Collar 2014) was previously placed in the genus Francolinus.

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.

IUCN Red List criteria met and history
Red List criteria met
Critically Endangered Endangered Vulnerable
- - C2a(i)

Red List history
Year Category Criteria
2023 Vulnerable C2a(i)
2016 Endangered B2ab(i,ii,iii,v);C2a(i)
2012 Endangered B2ab(i,ii,iii,v);C2a(i)
2010 Endangered B2a+b(i,ii,iii,v); C2a(i)
2008 Vulnerable B1a+b(i,ii,iii,v); C2a(i)
2004 Vulnerable
2000 Vulnerable
1996 Vulnerable
1994 Vulnerable
1988 Threatened
Species attributes

Migratory status not a migrant Forest dependency high
Land-mass type continent
Average mass -
Range

Estimate Data quality
Extent of Occurrence (breeding/resident) 23,400 km2 medium
Number of locations 4-5 -
Severely fragmented? no -
Population
Estimate Data quality Derivation Year of estimate
Population size 1000-2499 mature individuals poor estimated 2009
Population trend decreasing poor inferred -
Generation length 5.18 years - - -
Number of subpopulations 2-100 - - -
Percentage of mature individuals in largest subpopulation 1-89% - - -

Population justification: No records of this species exist between 1971 and 2005, when c. 10 individuals were recorded (seven birds were seen and another pair or group were heard) at Mts Moco and Soque (Mills et al. 2013). Surveys between 2005 and 2009 estimated that c. 75 pairs occur on Mt Moco (Mills et al. 2011). In 2010, a significant but unquantified population of individuals was discovered in the Namba Mountains, where the species was found to be fairly common, and which likely holds the largest population of this species (Mills et al. 2013). Individuals have also been recently recorded in Tundavala (eBird 2023), but it is not possible to quantify the population there based only on this information.
Overall, the global population has been estimated at between 462-1,050 pairs and 1,040-2,080 pairs, depending on the amount of forest cover left in Angola (M. Mills in litt. 2010, Mills et al. 2011). The latter is likely an over-estimate unless the species is tolerant of a wider range of habitats than is currently known, hence the global population is currently best placed in the band 1,000-2,499 mature individuals (M. Mills in litt. 2010). Further fieldwork is needed to improve the accuracy of the population size, but considering the small extent of suitable habitat present within the species' range and elevation limits (2,000-2,500 m), the species' population size is unlikely to be large.

Trend justification: The species is considered to be highly dependent on Afromontane forest edge habitat, specifically on forest edge undergrowth, and is only found in areas which contain, or are adjacent to Afromontane forest, and is therefore directly linked to its existence. The exception to this is on Mount Soque, where Afromontane forest has been completely lost; this area contained a remnant population of four pairs in 2005, using vegetation similar to that found in forest edge (e.g., dense scrub). This subpopulation is therefore likely to be non-functional and an extinction debt generated from the clearance of the forest.
Due to land use change for grazing and agriculture and forest fires, which may be exacerbated in the future by climate change, Afromontane forest, within the physically restricted elevation limits of the species (which is confined to the highland plateaux or 'sky islands'), is estimated to be undergoing a decline of approximately 11% over the species' past three generations (16 years), 19% between 2022 and 2037, and 15% over the next three generations (Powell et al. 2023, Global Forest Watch 2023, using Hansen et al. [2013] data and methods disclosed therein). Although it could be argued that forest loss would equate to higher areas of forest edge habitat, as most forest loss is artificial, it is considered unlikely that the edge undergrowth specific to this species' habitat would be able to establish and mature enough, and over a sufficient amount of time on average for the species to disperse and reproduce sufficiently to contribute to a stabilisation or increase in the population size before this habitat is yet again destroyed, either at the same place or somewhere else.
Considering the species' dependence on Afromontane forest edge habitat, the absence of a functional population where this habitat has been removed, and the continuing loss of this habitat through land conversion and fires, it can be inferred that the species is undergoing a continuing decline in population size, which may also be exacerbated by some hunting pressure (Dean 2001; M. Mills in litt. 2005, 2010). Due to the uncertainty of the severity of the impact on the species caused by the loss of its habitat, and the potential for additional impact from hunting pressure, the rate of this decline has not been quantified.  


Country/territory distribution
Country/Territory Presence Origin Resident Breeding visitor Non-breeding visitor Passage migrant
Angola extant native yes

Important Bird and Biodiversity Areas (IBA)
Country/Territory IBA Name
Angola Mount Moco

Habitats & altitude
Habitat (level 1) Habitat (level 2) Importance Occurrence
Forest Subtropical/Tropical Moist Montane major resident
Grassland Subtropical/Tropical High Altitude suitable resident
Rocky areas (eg. inland cliffs, mountain peaks) suitable resident
Shrubland Subtropical/Tropical High Altitude major resident
Altitude 2000 - 2500 m Occasional altitudinal limits  

Threats & impact
Threat (level 1) Threat (level 2) Impact and Stresses
Agriculture & aquaculture Annual & perennial non-timber crops - Small-holder farming Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation, Ecosystem conversion
Biological resource use Hunting & trapping terrestrial animals - Intentional use (species is the target) Timing Scope Severity Impact
Ongoing Majority (50-90%) Negligible declines Low Impact: 5
Stresses
Species mortality
Biological resource use Logging & wood harvesting - Unintentional effects: (subsistence/small scale) [harvest] Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation
Climate change & severe weather Habitat shifting & alteration Timing Scope Severity Impact
Ongoing Whole (>90%) Slow, Significant Declines Medium Impact: 7
Stresses
Ecosystem degradation
Natural system modifications Fire & fire suppression - Increase in fire frequency/intensity Timing Scope Severity Impact
Ongoing Majority (50-90%) Slow, Significant Declines Medium Impact: 6
Stresses
Ecosystem degradation

Utilisation
Purpose Scale
Food - human subsistence, national

Recommended citation
BirdLife International (2024) Species factsheet: Swierstra's Spurfowl Pternistis swierstrai. Downloaded from https://datazone.birdlife.org/species/factsheet/swierstras-spurfowl-pternistis-swierstrai on 26/11/2024.
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 26/11/2024.