Taxonomic source(s)
Brooke, M. de L. 2004. Albatrosses and Petrels Across the World. Oxford University Press, Oxford.
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 |
---|---|---|
2022 | Near Threatened | A2cde; B2b(ii,iii) |
2016 | Near Threatened | A2ce; B2ab(i,ii,iii,v) |
2012 | Near Threatened | A2ce;B2ab(i,ii,iii,v) |
2010 | Near Threatened | A2c,e; B2a+b(i,ii,iii,v) |
2008 | Near Threatened | A2c,e; B2a+b(i,ii,iii,v) |
2005 | Near Threatened | |
2004 | Near Threatened | |
2000 | Vulnerable | |
1996 | Vulnerable | |
1994 | Vulnerable | |
1988 | Near Threatened |
Migratory status | full migrant | Forest dependency | does not normally occur in forest |
Land-mass type |
shelf island |
Average mass | 408 g |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 38,400 km2 | medium |
Extent of Occurrence (non-breeding) | 2,500,000 km2 | medium |
Area of Occupancy (breeding/resident) | 504 km2 | medium |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 200000-299999 mature individuals | medium | estimated | 2016 |
Population trend | stable | poor | suspected | - |
Rate of change over the past 10 years/3 generations (longer of the two periods) | 24% | - | - | - |
Generation length | 13.5 years | - | - | - |
Number of subpopulations | 6 | - | - | - |
Percentage of mature individuals in largest subpopulation | 95-99% | - | - | - |
Population justification: The vast majority of the population (>95%) breeds on Natividad (Keitt 1998). On the San Benito islands, there used to be at least several thousand pairs (B. Tershy and B. Keitt in litt. 1999), but only 250-500 pairs were estimated in 1991 (Everett and Anderson 1991), and during the 2017-2019 breeding season, 121 breeding pairs were estimated (Sánchez et al. 2021a). On Guadalupe, the population was estimated at 2,500 pairs in 1991 (Everett and Anderson 1991), although may now be extirpated here (Sánchez et al. 2021a). In 1927, nesting was reported in Isla Rasa, Gulf of California, but the species is believed to be extirpated from that island by introduced rodents (Velarde et al. 2015). Nesting has been reported again since 2010; however, the size of the nesting population has not been determined (Velarde et al. 2015).
The total population estimated in 1998-1999 was around 80,000 pairs, and therefore 160,000 mature individuals. However, it is likely that the methods used in 1998-99 overestimated the population size, as counts of nests in selected areas were extrapolated to the whole surface of the island used by birds, without considering that there were large areas without any burrows.
In 2016, aerial photography and GIS were used to count the total number of occupied and unoccupied burrows in Natividad Island during the breeding season (Albores-Barajas et al. 2016). The total number of burrows counted, including occupied and abandoned burrows, was 56,400, but with a relatively low occupancy (between 75% and 50% depending on the area). The counts gave a figure of 37,900 (± 8500 SE) breeding pairs, equating to about 75,800 mature individuals. This figure was based on the initial occupancy of burrows in February 2016. Of these initially occupied burrows, 4,500 (about 12%) were later abandoned (Albores-Barajas et al. 2016). During the 2017-2019 breeding season, through further surveys on nest or burrow densities, 118,920 breeding pairs were counted on Natividad (Sánchez et al. 2021a), roughly equating to 238,000 mature individuals. Given the small populations present on other islands off Mexico's Pacific coast, the population is therefore placed in the band 200,000-299,999 mature individuals.
Trend justification: The species declined dramatically in the past owing to predation, in particular by introduced cats. On the principal breeding island, Natividad, there was a 15% decrease in habitat and a 13-20% loss in burrows between 1970 and the mid-1990s, with an estimated population decline of 4% per annum (Keitt 1998). However, eradication of cats from Natividad in 2002-2003 suggests that immediate threats to the species have now been significantly reduced and recruitment to the population may have increased. Nevertheless, the current trend has not been quantified. Although the counts from 2016 are much lower than in 1998-1999, data from 1998-1999 apparently overestimated the population; thus, the data do not seem to be comparable. However, as the eradication of cats from Natividad achieved a 90% reduction in mortality and a rapid recolonisation of cat-free areas (Keitt and Tershy 2003, Keitt et al. 2006), it is tentatively suspected that the population is currently stable or increasing slowly. Nevertheless, due to the species' longevity, the rapid declines of 4% per year in the large majority of the breeding population up until 2002 equate to a reduction of c.24% over the past three generations (40.5 years). Notably, bycatch in fisheries, habitat loss to infrastructure developments and habitat degradation through anthropogenic disturbance and introduced mammals and birds remain ongoing threats, and while their impacts on the population size have not been quantified it is possible that the population is still declining locally.
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
Canada | extant | vagrant | yes | |||
Mexico | extant | native | yes | yes | ||
USA | extant | native | yes |
Country/Territory | IBA Name |
---|---|
Mexico | Archipiélago Bahía de los Angeles |
Mexico | Archipiélago Loreto |
Mexico | Área de San Quintín |
Mexico | Bahía e Islas de San Jorge |
Mexico | Bahía Magdalena-Almejas |
Mexico | Bahía Todos Santos |
Mexico | Ensenada de la Paz |
Mexico | Isla Asunción |
Mexico | Isla Cedros |
Mexico | Isla Natividad |
Mexico | Isla San Pedro Mártir |
Mexico | Isla San Roque |
Mexico | Islas Coronado |
Mexico | Islas San Benito |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Caves and Subterranean Habitats (non-aquatic) | Caves | suitable | breeding |
Marine Neritic | Macroalgal/Kelp | suitable | non-breeding |
Marine Neritic | Macroalgal/Kelp | suitable | breeding |
Marine Neritic | Pelagic | major | non-breeding |
Marine Neritic | Pelagic | major | breeding |
Marine Neritic | Seagrass (Submerged) | suitable | non-breeding |
Marine Neritic | Seagrass (Submerged) | suitable | breeding |
Marine Neritic | Subtidal Loose Rock/pebble/gravel | suitable | non-breeding |
Marine Neritic | Subtidal Loose Rock/pebble/gravel | suitable | breeding |
Marine Neritic | Subtidal Rock and Rocky Reefs | suitable | non-breeding |
Marine Neritic | Subtidal Rock and Rocky Reefs | suitable | breeding |
Marine Neritic | Subtidal Sandy | suitable | non-breeding |
Marine Neritic | Subtidal Sandy | suitable | breeding |
Marine Neritic | Subtidal Sandy-Mud | suitable | non-breeding |
Marine Neritic | Subtidal Sandy-Mud | suitable | breeding |
Marine Oceanic | Epipelagic (0-200m) | major | non-breeding |
Marine Oceanic | Epipelagic (0-200m) | major | breeding |
Marine Oceanic | Mesopelagic (200-1000m) | major | non-breeding |
Marine Oceanic | Mesopelagic (200-1000m) | major | breeding |
Shrubland | Subtropical/Tropical Moist | major | breeding |
Altitude | 0 - 100 m | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Biological resource use | Fishing & harvesting aquatic resources - Unintentional effects: (subsistence/small scale) [harvest] | Timing | Scope | Severity | Impact | ||||
Ongoing | Whole (>90%) | Slow, Significant Declines | Medium Impact: 7 | ||||||
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Human intrusions & disturbance | Recreational activities | 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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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Canis familiaris | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Capra hircus | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Whole (>90%) | Slow, Significant Declines | Past Impact | ||||||
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Equus asinus | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Whole (>90%) | Slow, Significant Declines | Past Impact | ||||||
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Felis catus | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Majority (50-90%) | Rapid Declines | Past Impact | ||||||
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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%) | Slow, Significant Declines | Past Impact | ||||||
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Ovis aries | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Whole (>90%) | Slow, Significant Declines | Past Impact | ||||||
|
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Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Corvus corax | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Negligible declines | Low Impact: 5 | ||||||
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Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Larus occidentalis | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Negligible declines | Low Impact: 5 | ||||||
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Pollution | Excess energy - Light pollution | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
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Residential & commercial development | Commercial & industrial areas | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Majority (50-90%) | Rapid Declines | Past Impact | ||||||
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Residential & commercial development | Housing & urban areas | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Slow, Significant Declines | Medium Impact: 6 | ||||||
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Transportation & service corridors | Roads & railroads | Timing | Scope | Severity | Impact | ||||
Past, Likely to Return | Minority (<50%) | Slow, Significant Declines | Past Impact | ||||||
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Recommended citation
BirdLife International (2024) Species factsheet: Black-vented Shearwater Puffinus opisthomelas. Downloaded from
https://datazone.birdlife.org/species/factsheet/black-vented-shearwater-puffinus-opisthomelas on 23/11/2024.
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 23/11/2024.