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Megadyptes antipodes 

Scope: Global
Language: English
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Taxonomy [top]

Kingdom Phylum Class Order Family
Animalia Chordata Aves Sphenisciformes Spheniscidae

Scientific Name: Megadyptes antipodes
Species Authority: (Hombron & Jacquinot, 1841)
Common Name(s):
English Yellow-eyed Penguin
Spanish Pingüino ojigualdo o de ojo amarillo
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. Lynx Edicions BirdLife International, Barcelona, Spain and Cambridge, UK.
Identification information: 65 cm. Medium-sized penguin with pale yellow eye. Pale yellow head with black feather shafts. Band of bright yellow from eyes around back of head. Juvenile has greyer head with no band. Similar spp. Distinctive from other crested penguins in range. Voice Slightly musical compared to other penguin species.

Assessment Information [top]

Red List Category & Criteria: Endangered B2ab(ii,v)c(iv) ver 3.1
Year Published: 2016
Date Assessed: 2016-10-01
Assessor(s): BirdLife International
Reviewer(s): Butchart, S. & Symes, A.
Contributor(s): Ellenberg, U., Houston, D., Lalas, C., Mattern, T., McKinlay, B., Ratz, H., Seddon, P., Webster, T., Young, M. & van Heezik, Y.
Facilitator/Compiler(s): Benstead, P., Calvert, R., Mahood, S., McClellan, R., Moreno, R., Seddon, P., Taylor, J.
Justification:
This species is listed as Endangered because it is confined to a very small range when breeding, in which its forest/scrub habitat has declined in quality. Its population has undergone extreme fluctuations and is now thought to be in overall decline.

Previously published Red List assessments:

Geographic Range [top]

Range Description:Megadyptes antipodes is endemic to New Zealand where it breeds on the South Island's south-east coast (452 pairs in 2011-/12 (Seddon et al. 2013), Stewart Island and outliers (178 pairs in 1999-2001; Massaro and Blair 2003), the Auckland Islands group (520-570 pairs in 1989; Moore 1992) and Campbell Island (350-540 pairs in 1992; Moore 2001, Seddon et al. 2013). The South Island population is genetically distinct from the two sub-Antarctic populations (inferred immigration rate 0.003 per generation; Boessenkool et al. 2010). Adults are sedentary and generally forage within 50 km of their breeding colonies (Mattern et al. 2007), but juveniles may disperse north as far as the Cook Strait (Marchant and Higgins 1990). 

Countries occurrence:
Native:
New Zealand
Additional data:
Estimated area of occupancy (AOO) - km2:380Continuing decline in area of occupancy (AOO):Yes
Extreme fluctuations in area of occupancy (AOO):NoEstimated extent of occurrence (EOO) - km2:395000
Continuing decline in extent of occurrence (EOO):NoExtreme fluctuations in extent of occurrence (EOO):No
Number of Locations:12Continuing decline in number of locations:No
Extreme fluctuations in the number of locations:No
Upper elevation limit (metres):75
Range Map:Click here to open the map viewer and explore range.

Population [top]

Population:There are estimated to be 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). There is very little movement between the mainland and sub-Antarctic and genetic analyses reveal three distinct sub-populations (mainland New Zealand including Stewart Island, and the sub-Antarctic Auckland and Campbell Islands), which should be managed as separate conservation units (Boessenkool et al. 2009). Little is known about the suspected “species stronghold” on the sub-Antarctic Islands. The Auckland Islands population has never seen a comprehensive census but judging from a brief reconnaissance in 1989 may support an estimated 520-570 pairs (Moore 1992). 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). Annual nest counts in most South Island breeding areas reveal considerable population fluctuations in the past; since 1996 the population has declined by 76% (Mattern et al. 2016). In 2015, a total of 216 breeding pairs were counted on the South Island (Melanie Young, DOC; unpublished data).    



Trend Justification:  The species is thought to be declining overall as a result of a number of threatening processes, principally introduced predators, habitat conversion and disturbance. Although survey results from South Island are not indicative of declines (but rather fluctuations), there is evidence of declines on Stewart Island (D. Houston in litt. 2012).

Current Population Trend:Decreasing
Additional data:
Number of mature individuals:3400Continuing decline of mature individuals:Yes
Extreme fluctuations:YesPopulation severely fragmented:Yes
No. of subpopulations:3Continuing decline in subpopulations:Unknown
Extreme fluctuations in subpopulations:NoAll individuals in one subpopulation:No

Habitat and Ecology [top]

Habitat and Ecology:In the South Island the species tends to nest in forest and scrub remnants, amongst pasture and in exotic vegetation (McKay et al. 1999; Ratz and Murphy 1999; Seddon et al. 2013). Nests generally have surrounding vegetation that conceals them from visual contact with conspecifics (Seddon and Davis 1989), but this is not believed to be a prerequisite for successful breeding (Clarke et al. 2015). Two eggs are laid from mid-September to mid-October, with hatching occurring at the beginning of November. Chicks fledge from mid-February to mid-March (Seddon et al. 2013).  Prey species on the mainland are primarily opalfish, sprat, silversides, ahuru, blue cod and arrow squid; red cod used to be an important prey species in the 1980s (van Heezik 1990, Moore and Wakelin 1997; Browne et al. 2011). Yellow-eyed penguins forage predominantly along the seafloor (87% of all dives) whereas pelagic dives mostly occur when they travel back to their breeding areas (Mattern et al. 2007). They occasionally dive deeper than 120m but predominantly forage in depths of less than 100 m (Seddon et al. 2013). Individuals have foraging sites they revisit on subsequent foraging trips and even between years (Moore 1999; Mattern et al. 2007). They appear very sensitive to disturbance and degradation of their benthic foraging habitat (Browne et al. 2011; Ellenberg and Mattern 2012; Mattern et al. 2013).  

Systems:Terrestrial; Marine
Continuing decline in area, extent and/or quality of habitat:No
Generation Length (years):7
Movement patterns:Not a Migrant

Threats [top]

Major Threat(s): Introduced ferret (Mustela furo), stoat (M. erminea),unleashed dogs (Canis lupus familiaris), and possibly feral cats (Felis catus), are predators in the South Island. Predation by pigs on the main Auckland Island and in the Catlins is known to occur (B. McKinlay per D. Houston in litt. 2012). Accidental fires in breeding areas are a known, but infrequent, threat. A rogue female New Zealand sea lion (Phocarctos hookeri) and her daughter had been estimated to eat 20-30 birds annually on the Otago Peninsula (Lalas et al. 2007), but they have since died of natural causes. Repeated adult die-off events remain little understood but might be due to toxins (Gill and Darby 1993). Disease appears to be a problem in some populations in some years, with diphtheritic stomatitis (caused by the bacteria Corynebacterium spp.) and the blood parasite Leucocytozoon tawaki (formerly only known from Fiordland penguins) major causes of mortality for chicks (Argilla et al. 2013). Human disturbance, particularly from unregulated tourists at breeding areas, negatively affects energy budgets, fledgling weight and probability of survival (McClung et al. 2004; Ellenberg et al. 2007, 2009, 2013). By-catch mortality in the commercial gillnet fisheries is an unquantified but potentially significant cause of mortality (Darby and Dawson 2000; Ellenberg and Mattern 2012). Furthermore, fisheries activities appear to affect prey availability and prey quality (Mattern 2007; Browne et al. 2011), and influence penguin foraging behaviour (Mattern et al. 2013). There is a suspected but unconfirmed link between changing sea surface temperature and penguin vital rates, whereby productivity and survival are projected to decline under predicted climate change (Mattern et al. 2016). 

Conservation Actions [top]

Conservation Actions:

Conservation Actions Underway

Conservation management projects are and have been undertaken in the South Island by or under NZ Department of Conservation (DOC) approvals. The Yellow-eyed Penguin Trust was formed to raise awareness and funds and now in conjunction with DOC undertakes predator control and coastal revegetation. Many mainland sites have been fenced to minimize disturbance by farm stock and to facilitate vegetation restoration. Predator trapping is intensive during the breeding season at 50% of South Island sites, and habitat is being restored (Seddon et al. 2013). Some sites subject to unregulated visitor disturbance are either closed during critical periods, or patrolled by volunteer wardens. Improved signage and visitor guidelines are promoted at key sites, but these tools are less effective at improving visitor behaviour than closure or strict regulation (Stein et al. 2010). Rehabilitation is undertaken at four mainland sites, including Penguin Place on the Otago Peninsula and Penguin Rescue in North Otago, to prevent losses due to starvation, injury and moult complications. There is a census of South Island colonies approximately every five years, and a census of selected sites annually (Taylor 2000).

Conservation Actions Proposed

Obtain reliable population estimates for the Auckland and Campbell Islands. Eradicate predators (pigs and cats) from the Auckland Islands. Quantify the impact of commercial fishing activity on yellow-eyed penguins (bycatch mortality in gillnets and the influence of bottom disturbance by trawling/dredging on penguin behaviour and food quality). Regulate tourist access to breeding colonies. Develop a comprehensive understanding of the spatial and temporal extent of at-sea distribution during critical seasons (e.g. breeding, pre-moult, winter) and life-history stages (e.g. juvenile dispersal) to quantify fisheries overlap. Derive up to date data on important diet species throughout the range to evaluate changing patterns of foraging and diet, and assess the implications of climate change on marine productivity of relevance for the species.



Citation: BirdLife International. 2016. Megadyptes antipodes. The IUCN Red List of Threatened Species 2016: e.T22697800A93640603. . Downloaded on 10 December 2016.
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