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.
Turbott, E.G. 1990. Checklist of the Birds of New Zealand. Ornithological Society of New Zealand, Wellington.
Critically Endangered | Endangered | Vulnerable |
---|---|---|
- | A2ade+4abde | A2ade+3bde+4abde |
Year | Category | Criteria |
---|---|---|
2020 | Endangered | A2ade+4abde |
2018 | Endangered | A2ade; B2ab(ii,iii,v)c(iv) |
2016 | Endangered | B2ab(ii,v)c(iv) |
2012 | Endangered | B2b(iii,v)c(iv) |
2010 | Endangered | B2b(iii)+c(iv) |
2008 | Endangered | B2b(iii)+c(iv) |
2007 | Endangered | |
2005 | Endangered | |
2004 | Endangered | |
2000 | Endangered | |
1996 | Vulnerable | |
1994 | Vulnerable | |
1988 | Threatened |
Migratory status | not a migrant | Forest dependency | medium |
Land-mass type | Average mass | - |
Estimate | Data quality | |
---|---|---|
Extent of Occurrence (breeding/resident) | 395,000 km2 | medium |
Number of locations | 8-9 | - |
Severely fragmented? | no | - |
Estimate | Data quality | Derivation | Year of estimate | |
---|---|---|---|---|
Population size | 2600-3000 mature individuals | medium | estimated | 2020 |
Population trend | decreasing | medium | inferred | 1992-2021 |
Rate of change over the past 10 years/3 generations (longer of the two periods) | 50-79% | - | - | - |
Rate of change over the future 10 years/3 generations (longer of the two periods) | 30-49% | - | - | - |
Rate of change over the past & future 10 years/3 generations (longer of the two periods) | 50-79% | - | - | - |
Generation length | 9.9 years | - | - | - |
Number of subpopulations | 2 | - | - | - |
Percentage of mature individuals in largest subpopulation | 1-89% | - | - | - |
Population justification: Past estimates suggested there were around 1,700 breeding pairs (3,400 breeders), with an estimated 60% of these in the sub-Antarctic (Auckland Campbell Islands) (Seddon et al. 2013), but recent declines on mainland New Zealand indicate the total population is lower that previously thought. Surveys in the Auckland Islands in 2017 estimated 577 pairs (Muller et al., 2020). The Campbell Island population was last estimated in 1992 at 350-540 pairs (Moore 2001). Stewart Island and outliers were estimated at 220-400 pairs in 1994, dropping to 178 pairs in 1999-2001 (Massaro and Blair 2003). In 2011-2012 South Island's south-east coast was thought to hold 452 pairs (Seddon et al. 2013), in 2015, there were 252 breeding pairs counted on the South Island, while in 2019, the total number of breeding pairs counted in the South Island was 227 (DOC; unpublished data). Based on these most recent estimates, the global population is estimated to be in the range of 2,684 - 3,064 mature individuals, rounded here to 2,600 - 3,000 mature individuals.
There is very little movement between the mainland and sub-Antarctic and genetic analyses reveal two distinct sub-populations (mainland New Zealand including Stewart Island, and the sub-Antarctic Auckland and Campbell Islands; Boessenkool et al. 2009).
Trend justification: The species is thought to be declining overall as a result of a number of threatening processes, principally introduced predators, habitat conversion, changes in the marine environment, and disturbance.
It has been suggested that the population on the South Island may show fluctuations, but population modelling of a well-studied colony on the Otago Peninsular showed rather that a dramatic decline has taken place: a 76% decline between 1996 and 2015 (Mattern et al., 2017). A consolidation of breeding numbers over the past 20 years in light of this decline reinforces the concern (New Zealand Department of Conservation [DOC] 2020, Te Rūnanga o Ngāi Tahu, Department of Conservation, Yellow-eyed Penguin Trust, and Fisheries New Zealand. 2020): in 1999 there were 741 breeding pairs in the northern population (including Stewart Island/Rakiura and surrounding islands), while the total recorded in 2019 is 265 pairs. This is equivalent to a 78.5% decline over three generations (29.7 years, after Bird et al. 2020). The decline appears to have accelerated after 2012: a 52% decline was recorded across the South Island between 2012 and 2019 (Seddon et al. 2013, DOC unpublished data, 2020). In 2011-2012 South Island's south-east coast was thought to hold 452 pairs (Seddon et al. 2013), in 2015, there were 252 breeding pairs counted on the South Island, while in 2018/2019, the total number of breeding pairs counted in the South Island was 227 (DOC; unpublished data). On Te Rere, Southland, the population has declined from 81 individuals in 2008, to 20 in 2018 and nests from 23 to 5 in the same time (Wood, 2018). The population size on Stewart Island and outliers were estimated at 220-400 pairs in 1994, dropping to 178 pairs in 1999-2001 (Massaro and Blair 2003).
Trajectories in the sub-Antarctic populations are not known but there is no evidence of declines on the Auckland islands between 1989 and 2017 (Moore 1992, Muller et al. 2020). The Campbell Island population has not been assessed since 1992. In light of the very rapid declines in the northern population and poor knowledge of the southern, overall declines are suspected to fall in the range 50-79% over the past three generations (29.7 years). These declines are likely to continue at this rate in the near future, however they are of such magnitude in the north that the contribution of this population to the overall population size will mean that the future rate of decline is suspected to be at a reduced rate.
Country/Territory | Presence | Origin | Resident | Breeding visitor | Non-breeding visitor | Passage migrant |
---|---|---|---|---|---|---|
New Zealand | extant | native | yes |
Country/Territory | IBA Name |
---|---|
New Zealand | Adams Island |
New Zealand | Aramoana Otago Harbour |
New Zealand | Auckland Islands 2 (near-shore) |
New Zealand | Banks Peninsula |
New Zealand | Campbell Islands |
New Zealand | Campbell Islands (nearshore) |
New Zealand | Canterbury (offshore) |
New Zealand | Catlins Coast |
New Zealand | Dunedin Coast (offshore) |
New Zealand | Enderby Group |
New Zealand | Main Auckland Island |
New Zealand | Moeraki Katiki Point |
New Zealand | North Coast Rakiura |
New Zealand | North Otago |
New Zealand | North Otago (offshore) |
New Zealand | Northern Titi Muttonbird Islands |
New Zealand | Otago Peninsula |
New Zealand | Paterson Inlet The Neck |
New Zealand | Port Adventure |
New Zealand | Port Pegasus |
New Zealand | Rakiura (offshore) |
New Zealand | Raratoka Centre Island |
New Zealand | Ruapuke |
New Zealand | South Otago (offshore) |
New Zealand | Southern South Island (offshore) |
New Zealand | Whenua Hou Codfish Island |
Habitat (level 1) | Habitat (level 2) | Importance | Occurrence |
---|---|---|---|
Artificial/Terrestrial | Pastureland | suitable | resident |
Forest | Subantarctic | major | breeding |
Forest | Temperate | major | breeding |
Marine Neritic | Pelagic | major | resident |
Marine Oceanic | Epipelagic (0-200m) | major | resident |
Shrubland | Subantarctic | major | resident |
Shrubland | Temperate | major | breeding |
Altitude | 0 - 75 m | Occasional altitudinal limits |
Threat (level 1) | Threat (level 2) | Impact and Stresses | |||||||
---|---|---|---|---|---|---|---|---|---|
Agriculture & aquaculture | Livestock farming & ranching - Agro-industry grazing, ranching or farming | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | No decline | Low Impact: 4 | ||||||
|
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Biological resource use | Fishing & harvesting aquatic resources - Unintentional effects: (large scale) [harvest] | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Rapid Declines | Medium Impact: 7 | ||||||
|
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Biological resource use | Fishing & harvesting aquatic resources - Unintentional effects: (subsistence/small scale) [harvest] | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Negligible declines | Low Impact: 4 | ||||||
|
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Biological resource use | Logging & wood harvesting - Unintentional effects: (subsistence/small scale) [harvest] | Timing | Scope | Severity | Impact | ||||
Past, Unlikely to Return | Minority (<50%) | Slow, Significant Declines | Past Impact | ||||||
|
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Climate change & severe weather | Habitat shifting & alteration | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Slow, Significant Declines | Medium Impact: 6 | ||||||
|
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Energy production & mining | Oil & gas drilling | Timing | Scope | Severity | Impact | ||||
Future | Minority (<50%) | Slow, Significant Declines | Low Impact: 3 | ||||||
|
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Human intrusions & disturbance | Recreational activities | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Canis familiaris | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Negligible declines | Low Impact: 5 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Erysipelothrix rhusiopathiae | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Slow, Significant Declines | Low Impact: 5 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Felis catus | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Negligible declines | Low Impact: 5 | ||||||
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Mustela erminea | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Negligible declines | Low Impact: 5 | ||||||
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Mustela furo | Timing | Scope | Severity | Impact | ||||
Ongoing | Majority (50-90%) | Negligible declines | Low Impact: 5 | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Plasmodium relictum | Timing | Scope | Severity | Impact | ||||
Past, Likely to Return | Majority (50-90%) | Causing/Could cause fluctuations | Past Impact | ||||||
|
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Invasive and other problematic species, genes & diseases | Invasive non-native/alien species/diseases - Sus domesticus | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Unknown | Unknown | ||||||
|
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Invasive and other problematic species, genes & diseases | Problematic native species/diseases - Phocarctos hookeri | 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 - Corynebacterium amycolatum | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Unknown | Unknown | ||||||
|
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Invasive and other problematic species, genes & diseases | Problematic species/disease of unknown origin - Named species | Timing | Scope | Severity | Impact | ||||
Ongoing | Minority (<50%) | Unknown | Unknown | ||||||
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Natural system modifications | Fire & fire suppression - Increase in fire frequency/intensity | Timing | Scope | Severity | Impact | ||||
Past, Likely to Return | Minority (<50%) | Negligible declines | Past Impact | ||||||
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Recommended citation
BirdLife International (2024) Species factsheet: Yellow-eyed Penguin Megadyptes antipodes. Downloaded from
https://datazone.birdlife.org/species/factsheet/yellow-eyed-penguin-megadyptes-antipodes on 22/11/2024.
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 22/11/2024.