Eastern rockhopper penguin
Eudyptes filholi Hutton, 1879
Geographical variation: Previously considered conspecific with western rockhopper penguin (E. chrysocome) and Moseley’s rockhopper penguin (E. moseleyi)
The eastern rockhopper penguin breeds on subantarctic islands in the New Zealand region (including Australia’s Macquarie Island) and in the Indian Ocean. Recent research has suggested that the eastern rockhopper penguin is genetically distinct from two closely-related species: the western (or southern) rockhopper penguin, which breeds on islands around southern South America and the Falkland Islands, and Moseley’s (or northern) rockhopper penguin, which breeds on a few temperate islands in the Atlantic and Indian Oceans. Taken together, rockhopper penguins have a broad circumpolar breeding distribution spanning 37-53° latitude. Large-scale population declines of each species occurred at many breeding sites across their range in the 20th Century, perhaps accelerating in recent decades. A global population of more than 5.5 million breeding pairs of rockhopper penguins declined to less than 1.5 million, including a dramatic decline at New Zealand’s Campbell Island.
Breeding sites of the eastern rockhopper penguin in the New Zealand region include Campbell, Auckland, Antipodes and Macquarie islands or island-groups. Eastern rockhopper penguins visit land only to breed and moult during the austral spring, summer, and early autumn, spending the remaining 5-6 months of the year at sea. Adult eastern rockhopper penguins tracked from Campbell Island travelled south-east or east during the over-winter period. The average maximum distance from Campbell Island was c.2,000 km, while the greatest was c.4,000 km. Several individuals travelled a total of c.15,000 km.
Eastern rockhopper penguins are readily identified as a species of ‘crested penguin’ (genus Eudyptes) by their spiky yellow crest feathers, black back, white front, and orange-brown bill. They are the smallest of the crested penguins. The yellow eye-brow stripe starts well back from the bill and is very thin until behind the eye, where it flares out as a crest that also includes long black feathers. Some crest feathers are pendulant, but barely reach as far as the black-white demarcation line on the throat (cf. Moseley’s rockhopper penguin). The two yellow crests are joined across the hind-crown by a shorter black occipital crest. The bare skin around the base of the bill (the gape) is pinkish-white in eastern rockhopper penguins. Although the bill is typically mostly orange-brown, in adults of the New Zealand region up to 90% of the lower mandible may be white, and a small amount of the distal end of the upper mandible may also be white. The eyes are red and the feet and legs are pinkish-white with black soles. Males and females differ primarily in bill size. Adult plumage is attained at 2 years of age. Fledglings (c.65 days old) are bluish black where they will later be black, and have a black bill and no obvious crest. In juvenile plumage (1-2 years of age), black parts may appear dark brown, the throat is mottled grey, the bill is smaller (mostly shallower) and more brown than orange, and the yellow crest feathers are short.
Voice: breeding adults make loud pulsing, braying calls often accompanied by ritualised displays. A short contact bark is given on land and at sea.
Similar species: within the New Zealand region, eastern rockhopper penguins are most similar to Snares crested penguin, which is larger with a more massive bill, duller red-brown eyes, and has broader eye-brow stripes that start closer to the bill. The Snares crested penguin also lacks an occipital crest. Western rockhopper penguin and Moseley’s rockhopper penguin are very rare vagrants to the region. The western rockhopper has black skin around the base of the bill, and the yellow over the eye is wedge-shaped or triangular (cf. thin and parallel-sided in eastern rockhopper). Adult Moseley’s rockhopper penguins have improbably long and luxuriant pendulant yellow crest feathers that reach well below the black-white demarcation line on the throat.
Distribution and habitat
Within the New Zealand region, eastern rockhopper penguins breed at Campbell, Auckland and Antipodes Islands, and nearby Macquarie Island. Elsewhere they breed on Heard, Kerguelen, Crozet, Marion and Prince Edward Islands (all in the southern Indian Ocean). They breed in colonies of tens to tens-of-thousands of nests, reaching densities of 2.4 nests per m2 on open ground. Colonies are often on steep slopes near the sea, with nests often among and under boulders below eroding cliffs. Nest may also be in caves and up to 200 m inland and 100 m above sea level. Nests are composed of pebbles, sometimes lined with vegetation. Where colonies form amongst vegetation such as tussock, fern, or mega-herbs, the penguin’s guano and trampling usually kills the plants and causes soil erosion down to bare rock over a decade or two. On Antipodes Island eastern rockhopper penguins mainly nest on the inland edges of colonies of the larger erect-crested penguin.
There are very few confirmed records from the New Zealand mainland, as few of the reported sightings clarified which of the three forms (now species) of rockhopper penguin the bird belonged to. The only confirmed record since the 1970s was an immature bird that moulted at Cape Palliser, Wairarapa, in January-February 2017.
Campbell Island formerly held the world’s largest population of eastern rockhopper penguins, but the population crashed by an estimated 95% between 1942 and 2012, from 800,000 to 33,200 breeding pairs. Although inter-colony trends varied greatly, the overall Cambpell Island population grew between c.1996 and 2012. In the 20th Century the population at the Antipodes Island was likely considerably larger than at the Auckland Islands, but both have experienced major declines in recent decades and both now apparently support fewer than 3,000 breeding pairs. In 2011 the Antipodes Island population was estimated to be c.2,900 breeding pairs. Population estimates at Macquarie Island have varied greatly over short time periods, but a large decline seems apparent there too, with a 2007 population estimate of c.37,500 breeding pairs.
Threats and conservation
Low food availability, resulting from climate change, is thought to be the main cause of eastern rockhopper penguin population declines. This is likely to be due to changes in oceanic productivity near breeding islands requiring adults to swim further offshore, spend more time foraging, or return with smaller food loads when provisioning young. Adults that are experiencing nutritional stress related to low food availability make longer foraging trips, and chicks that are fed less often grow more slowly. Predation by sea lions, fur seals, skuas, and giant petrels may have important impacts on some populations. On Campbell Island, predation by New Zealand sea lions of adult eastern rockhopper penguins is the most important driver of the ongoing decline of the main study colony. Oil spills pose a looming threat, especially if attempts are made to extract oil from seas south of New Zealand. Competition with commercial fisheries is a potential threat, but detailed data on diet and foraging distribution is lacking.
Eastern rockhopper penguins are monogomous, with shared incubation and chick care. They lay a 2-egg clutch with no re-laying or double-brooding. Eggs are laid about 4-5 days apart. Proper incubation does not begin until after the second egg is laid. The first laid (A-)egg averages only 72% the mass of the second-laid (B-)egg. Fledging of 2 chicks is rare (<4% of nests). Typically only the chick from the larger, slightly earlier-hatching B-egg survives to fledge. Males return to breeding colonies in the first-half of October, females about a week later. Males and females fast ashore until their incubation foraging trip, averaging 36 days and 44 days after arrival, respectively. They lay mainly in the first-half of November, 12-21 days after females return. The first incubation shift of 7-10 days is shared, after which the female performs the second (14-17 days), and the male the third (7-9 days). Incubation periods average 33.5 days for B-eggs, and 39 days for A-eggs. Males continue their c.34 day fast while guarding their chick, females provisioning the chick daily. The downy chicks (brown, with off-white bellies) form crêches when about 24 days old, and both sexes make daily, or less often multi-day, provisioning trips until the chick fledges at around 65 days old. When food is abundant a parent may provision chicks twice in the same day, especially if both chicks are alive. The majority of males make a 7-11 day self-feeding trip when chicks crêche before beginning provisioning. Sub-adult penguins may return to colonies to prospect in mid-December and come ashore again in mid- to-late January to moult on the periphery of colonies. Adults return to breeding colonies about a month after chicks fledge, and moult over 3-4 weeks in April.
Behaviour and ecology
Eastern rockhopper penguins are migratory, offshore-foragers. They are thought to feed mainly more than 10 km offshore from breeding colonies , but this has yet to be studied in detail.
Small fish, squid, octopus, and krill-like crustaceans were found in diet samples from adult eastern rockhopper penguins collected during the chick-rearing period on Campbell Island. Other populations may eat a greater proportion of crustaceans. In 1985–1986, Campbell Island chick diet samples were dominated by a single fish species, southern blue whiting (Micromesisteus australis)(75.6 % by number of prey).
BirdLife International. 2012. Species factsheet: Eudyptes moseleyi. 2012a [cited 24/07/2012 2012]. Available from http://www.birdlife.org.
BirdLife International. First assessment of endangered northern rockhopper penguins since 2011 oil spill. 2012b [cited 23 July 2012. Available from http://www.birdlife.org/community/2012/02/first-assessment-of-endangered-northern-rockhopper-penguins-since-2011-oil-spill/.
Cooper, J.; Brown, C.; Gales, R.; Hindell, M.; Klages, N.; Moors, P.; Pemberton, D.; Ridoux, V. Thompson, K.; van Heezik, Y. 1990. Diets and dietary segregation of crested penguins (Eudyptes). Pp 131-156 in Davis, L.S.; Darby, J.T. (eds) Penguin biology. Academic Press, San Diego.
Cooper, J. 1992. Rockhopper penguins at the Auckland Islands. Notornis 39: 66-67.
Crossin, G.T.; Trathan, P.N.; Phillips, R.A.; Dawson, A.; Le Bouard, F.; Williams, T.D. 2010. A carryover effect of migration underlies individual variation in reproductive readiness and extreme egg size dimorphism in Macaroni penguins. American Naturalist 176: 357-366.
Croxall, J.; Davis, L. 1999. Penguins: paradoxes and patterns. Marine Ornithology 27.
Cunningham, D. M.; Moors, P.J. 1994. The decline of rockhopper penguins Eudyptes chrysocome at Campbell Island, Southern Ocean and the influence of rising sea temperatures. Emu 94: 27-36.
Davis, L. S.; Renner, M. 2003. Penguins. Yale University Press, London.
de Dinechin, M.; Ottvall, R.; Quillfeldt, P.; Jouventin, P. 2009. Speciation chronology of rockhopper penguins inferred from molecular, geological and palaeoceanographic data. Journal of Biogeography 36: 693-702.
Dehnhard, N.; Poisbleau, M.; Demongin, L.; Ludynia, K.; Lecoq, M.; Masello, J.F.; Quillfeldt, P. 2013. Survival of rockhopper penguins in times of global climate change. Aquatic Conservation: Marine and Freshwater Ecosystems. 23:777–789.
Dehnhard, N.; Poisbleau, M.; Demongin, L.; Ludynia K.; Quillfeldt, P. 2014. High juvenile annual survival probabilities in southern rockhopper penguins Eudyptes chrysocome are independent of individual fledging traits. Ibis. 156:548–560.
Demongin, L.; Poisbleau, M.; Raya Rey, A.; Schiavini, A.; Quillfeldt, P.; Eens, M.; Strange, I.J. 2009. Geographical variation in egg size dimorphism in rockhopper penguins. Polar Biology 33: 469-476.
Hilton, G.M.; Thompson, D.R.; Sagar, P.M.; Cuthbert, R.J.; Cherel, Y.; Bury, S.J. 2006. A stable isotopic investigation into the causes of decline in a sub-Antarctic predator, the rockhopper penguin Eudyptes chrysocome. Global Change Biology 12: 611-625.
Hiscock, J.A.; Chilvers, B.L. 2014. Declining eastern rockhopper and erect-crested penguins on the Antipodes Islands, New Zealand. New Zealand Journal of Ecology 38:124-131.
Jouventin, P. 1982. Visual and vocal signals in penguins, their evolution and adaptive characters. Verlag Paul Parey, Berlin.
Jouventin, P.; Cuthbert, R.J.; Ottvall, R. 2006. Genetic isolation and divergence in sexual traits: evidence for the northern rockhopper penguin Eudyptes moseleyi being a sibling species. Molecular Ecology 15: 3413-3423.
Marchant, S.; Higgins, P.J. (eds.), 1990. Handbook of Australian, New Zealand and Antarctic birds. Vol. 1. Ratites to ducks. Melbourne, Oxford University Press.
Moors, P.; Merton, D. 1984. First records for New Zealand of Moseley's rockhopper penguin (Eudyptes chrysocome moseleyi). Notornis 31: 262-265.
Morrison, K.W. 2016. Individual repeatability in laying behaviour does not support the migration carry-over effect hypothesis of egg-size dimorphism in eastern rockhopper penguins. Journal of Avian Biology 70: 467-479.
Morrison, K.W.; Armstrong, D.P.; Battley, P.F.; Jamieson, S.E.; Thompson, D.R. 2017. New Zealand sea lion and brown skua predation is causing the continued decline of an eastern rockhopper penguin colony on Campbell Island. Polar Biology 40: 735-751.
Morrison, K.W.; Morrison, N.C.; Buchheit, R.M.; Dunn, R.; Battley, P.F.; Thompson, D.R. 2016. The canalized parental roles of a Eudyptes penguin constrain provisioning and growth of chicks during nutritional stress. Behavioral Ecology and Sociobiology 70: 467-479.
Morrison, K.W.; Battley, P.F.; Sagar, P.M.; Thompson, D.R. 2015. Population dynamics of eastern rockhopper pnguins on Campbell Island in relation to sea surface temperature 1942-2012: current warming hiatus pauses a long-term decline. Polar Biology 38: 163-177.
Morrison, K.W.; Bury, S.J.; Thompson, D.R. 2014. Higher trophic level prey does not represent a higher quality diet in a threatened seabird: implications for relating population dynamics to diet shifts inferred from stable isotopes. Marine Biology 161: 2243-2255.
Poisbleau, M.; Demongin, L.; Strange, I.J.; Otley, H.; Quillfeldt, P. 2008. Aspects of the breeding biology of the southern rockhopper penguin Eudyptes c. chrysocome and new consideration on the intrinsic capacity of the A-egg. Polar Biology 31: 925-932.
Pütz, K.; Raya Rey, A.; Schiavini, A.; Clausen, A.P.; Lüthi, B.H. 2006. Winter migration of rockhopper penguins (Eudyptes c. chrysocome) breeding in the Southwest Atlantic: is utilisation of different foraging areas reflected in opposing population trends? Polar Biology 29: 735-744.
Robertson, H.A; Baird, K.; Dowding, J.E.; Elliott, G.P.; Hitchmough, R.A.; Miskelly, C.M.; McArthur, N.; O’Donnell, C.F.J.; Sagar, P.M.; Scofield, R.P.; Taylor, G.A. 2017. Conservation status of New Zealand birds, 2016. New Zealand Threat Classification Series 19. Wellington, Department of Conservation. 27p.
Sagar, P.; Murdoch, R.; Sagar, M.; Thompson, D. 2005. Rockhopper penguin (Eudyptes chrysocome filholi) foraging at Antipodes Islands. Notornis 52: 75-80.
Sparks, J.; Soper, T. 1967. Penguins. David and Charles Ltd., London.
St. Clair, C.C. 1998. What is the function of first eggs in crested penguins? Auk 115: 478-482.
Tennyson, A.J.D.; Miskelly, C.M. 1989. "Dark-faced" rockhopper penguins at the Snares Islands. Notornis 36: 183-189.
Thiebot, J. B.; Cherel, Y.; Trathan, P.N.; Bost, C.A. 2012. Coexistence of oceanic predators on wintering areas explained by population-scale foraging segregation in space or time. Ecology 93: 122-130.
Warham, J. 1972. Breeding seasons and sexual dimorphism in rockhopper penguins. Auk 89: 86-105.
Warham, J. 1975: The crested penguins. Pp. 189-269 in Stonehouse, B. (ed.). The biology of penguins. Macmillan, London.
Watson, G.E. 1975. Birds of the Antarctic and Sub-Antarctic. American Geophysical Union, Washington.
Williams, T.D. 1995. The penguins: Spheniscidae. Oxford University Press, Oxford.
Morrison, K.W. 2013 [updated 2017]. Eastern rockhopper penguin. In Miskelly, C.M. (ed.) New Zealand Birds Online. www.nzbirdsonline.org.nz
Eastern rockhopper penguin
- Social structure
- Breeding season
- Nest type
- lined scrape, rock crevice, scrape
- Nest height (mean)
- 0 m
- Nest height (min)
- 0 m
- Nest height (max)
- 0 m
- Maximum number of successful broods
- Clutch size (mean)
- Clutch size (min)
- Clutch size (max)
- Mean egg dimensions (length)
- 66.9 mm
- Mean egg dimensions (width)
- 50.4 mm
- Egg colour
- White frequently stained brown and green with dirt and guano
- Egg laying dates
- Interval between eggs in a clutch
- 4.5 days
- Incubation behaviour
- Incubation length (mean)
- 33.5 days
- Incubation length (min)
- 30 days
- Incubation length (max)
- 41 days
- Nestling type
- Nestling period (mean)
- 65 days
- Age at fledging (mean)
- 65 days
- Age at independence (mean)
- 65 days
- Age at first breeding (typical)
- Maximum longevity
- 23 years
- Maximum dispersal
- >3000 km from breeding colony over winter