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Southern Giant-Petrel Macronectes giganteus Scientific name definitions

Carles Carboneras, Francesc Jutglar, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated July 16, 2014

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Introduction

The Southern Giant-Petrel is, as the name implies, the southern half of the giant-petrel superspecies. Both species are broadly sympatric over much of the Southern Oceans but the Southern Giant-Petrel is the more Antarctic of the two species. It breeds primarily in the South Atlantic and Indian Oceans as well as coastal extreme southern South America and Antarctica. The largest members of their family, Procellariidae, the giant-petrels are behaviorally distinct. They feed primarily on carrion for which they scavenge by plying the near shore waters of Southern Ocean coastlines searching for seal and penguin carcasses that have been washed ashore. Generally the larger of the two species, the Southern Giant-Petrel has two distinct color morphs, dark and white, the white morph accounting for up to 15% of some breeding populations.

Field Identification

85–100 cm (1); male 5 kg, female 3.8 kg; wingspan 150–210 cm (1). Huge , mollymawk-sized petrel with large and strong bill. Adult plumage is generally greyish brown, paler and even largely whitish but more or less spotted on head to upper breast, underparts dark towards rear; base of outer remiges silvery on underwing; iris dark brown to, more often, pale grey ; bill very pale brownish to pale pinkish, with scarcely darker but more greyish or greenish-grey tip; legs dark grey to dusky straw-grey. White morph forms up to 15% of individuals in certain localities; plumage entirely white except variable number of dark brown to black feathers scattered over body, wing-coverts and sometimes flight feathers (1); diagnostic, as white morph absent in M. halli, and birds with all-white head and neck probably also only referrable to present species (1). Otherwise best separated from M. halli by bill colour; also note contrasts in body plumage and the pattern of the head and underwing (2). Female averages smaller, especially in bill length, but also tarsus and tail measurements, and mass (1); in adults, male 40% heavier than female and consistently larger in all measurements (by 5–15%) (3). Juvenile uniform blackish sooty-brown , with dark iris; progressively acquires more pale brown and white in plumage, with full adult plumage perhaps only achieved when 7–13 years old (1).

Systematics History

For long considered conspecific with sibling M. halli, with which known to have hybridized on occasions. Populations breeding in S Atlantic (S Argentina, Falkland Is, and Gough I) may merit subspecific status as race solanderi (4, 5). Monotypic.

Subspecies

Monotypic.

Distribution

Circumpolar in Southern Ocean, breeding in Antarctica and from S Chile and S Argentina E through subantarctic islands to Heard I and Macquarie I.

Habitat

Marine , ranging from coastal to pelagic waters; occurs S into regions of pack ice and N into subtropical zone. Breeds on open coastal plateaux and also headlands, usually occupying grassy or bare ground, often in exposed situations, provided they are ice-free (6), but sometimes within dense Poa tussock grass (1). Feeds along coast during most of year.

Movement

Adults probably move little, dispersing only to adjacent waters and generally keeping further S than M. hallli, although there is some evidence that numbers at Antaractic sites are reduced in midwinter (6); juveniles may follow prevailing winds E around Southern Ocean, perhaps completing several circumnavigations prior to their first return to the colony (7). Immatures move further N than adults, regularly reaching 20º S (6) and subtropical seas, typically following cold-water currents off S Africa and W South America, and recorded N to St Helena (15º S) in C Atlantic (8). In Pacific, recorded N to New Guinea, Fiji, Tahiti, Raoul I (Kermadecs) (9) and Easter I (10), and is rare visitor to SW Indian Ocean, N to Seychelles (11). Most ringing recoveries of birds banded in Indian Ocean have been in Australian and New Zealand waters (7, 12) (nevertheless, a bird ringed on Macquarie was recovered in Uruguay and birds ringed in Argentina, South Orkneys, South Georgia and Antarctic Peninsula have been recovered in Brazil) (13, 14), while young ringed at Patagonian colonies have also been recovered in these areas, but are mainly resighted in SW Atlantic waters (15), and birds ringed in Antarctica have been recovered in wide variety of areas including Australia, South Africa, New Zealand and South America (16). No definite records from N Hemisphere, though a bird off Ushant, France, in Nov 1967, was formerly accepted as M. halli (now only as Macronectes sp.) (17); another giant petrel at Midway Atoll, Hawaii, in 1959, 1961 and 1962 not identified to specific level.

Diet and Foraging

Carrion , especially carcasses of seals (Arctocephalus) but also whales (Eubalaena australis) (18), penguins (Eudyptes, Spheniscus magellanicus (19), young Aptenodytes) and petrels (Daption, Fulmarus, Thalassoica, Pachyptila, Pelecanoides); some birds killed by battering or drowning, e.g. Daption, Black-faced Sheathbill (Chionis minor) (20), Imperial Shags (Phalacrocorax atriceps), Kelp Gulls (Larus dominicanus) (19) and even immatures of some smaller albatrosses (Diomedea), which are grasped by head (1, 21). Also takes cephalopods, krill, offal, discarded fish and galley refuse from ships; some food probably located by smell (6). Perhaps some variation in dietary composition by season and perhaps region, with summer dominated by birds (mostly penguins), followed by crustacea (mainly krill), fish, mammals and cephalopods (22), whereas winter diet is poorly known, more fish may be taken at South Georgia, although penguins remain important on Marion I at this season; males take more carrion and less marine food than females, although sexual differences in foraging behaviour are less marked than in M. halli, and latter is also typically more gregarious while foraging (6). Recent work in Patagonia and Antarctica using stable isotopes suggests that sex-specific differences in foraging are noticeable only in summer and that chicks are preferentially fed penguin and seal prey, which are less important in adult diet (23); study using satellite telemetry off Argentina found that females spent more time in the shelf break and exploited deeper waters than males, whereas males spent more time in coastal areas and showed higher spatial overlap with areas of high squid density than females (24). During breeding season, females undertake longer foraging trips than males (25). At sea feeds mostly by surface-seizing, which technique may be used to take sleeping or disabled birds (6), but also observed pursuit-diving to forage on carcasses (26). Associates with cetaceans, including killer whales (Orcinus orca) (27) and minke whales (Balaenoptera acutorostrata) (28). Frequents trawling grounds and sewage outfalls, and typically occurs alone or in small groups of up to five birds (1), although may aggregate into larger groups in non-breeding season (29).

Sounds and Vocal Behavior

Gives variety of whinnying, growling, guttural and braying calls, the former likened to a neighing colt, generally similar to those of M. halli, although it has been suggested that threat and appeasement displays might be better developed in the present species, which is also considered to have generally softer and higher-pitched vocalizations (6, 1). Cat-like mewing sounds given during confrontational displays (1). Utter various croaking sounds when competing for food at sea (1).

Breeding

Starts Sept/Oct (typically six weeks later than in M. halli) (1), though some birds (often failed breeders from previous season) can arrive at colonies as early as late Jul, with females undertaking 12-day pre-laying exodus, egg-laying lasts c. 1 month (and is typically later at higher latitudes, thus mean dates of 26–29 Sept on Marion I but 8–11 Nov on South Georgia) (6) and in Argentina chicks fledge between mid Mar and late Apr (30). Degree of natal philopatry not accurately known, but suspected to be high (6), although birds have been recovered at colonies up to 1400 km from their natal area (31). Monogamous and forms long-term pair-bonds (1). Forms loose colonies of up to 300 pairs (typically only 40 pairs) (6), occasionally single pairs (32, 33); nest (constructed by both sexes) is small mound of stones or rough pile of Poa tussock grass, 150 cm wide, with small depression on top (6). Single white egg, mean size 96·7–109·3 mm × 61·2–70·5 mm (34), mass 260·6 g (6); incubation 55–66 (mean 61) days, with c. 11 stints of 2–12 days becoming shorter as incubation progresses (6); chicks have white down, more ashy grey when older, brooded for 2–3 weeks, fed at any time of day or night, mostly in afternoon and least frequently between 00.00 h and 03.00 h, with male chicks being fed 1·6–2·4 times per day (depending on age) a meal of 170–460 g, whereas female young are fed meals of 130–400 g on average 1·2–3·3 times per day (35); fledging 104–132 days, with males fledging on average later than females (c. 123 days versus 117 days) and at greater weight, 4840 g versus 4020 g (6). One case of chick adoption recorded, but neither of the two young survived to fledge (36). At one Antarctic colony, mean lengths of foraging trips in excess of 200 km were 2600 km and 3000 km over two breeding seasons (25), but in Patagonia maximum distance travelled from the colonies was < 700 km and mean distance was 200 km (37). Breeding success averages an estimated 88% in Argentina (with chick survival 100% after day 45) (30) and 70% at South Georgia, but just 31% on Marion I (6), and recorded as 52% on South Shetland Is (34). Natural predators of eggs and chicks include Kelp Gulls (Larus dominicanus) (38), while climatic events such as blizzards can cause widespread nesting failure (31). Sexual maturity generally at 4–8 years, although mean is > 11 years on Macquarie I, while first return to colony is when 2·5–5 years old, with some evidence to suggest that males may commence to breed first. Annual adult survival variously estimated at 90–96%, whereas that of pre-breeders is less than 90%, while up to 30% of breeding-age adults may elect to skip a season on South Georgia (6).

Not globally threatened (Least Concern). Formerly classified as Vulnerable. Total population c. 30,575 breeding pairs (based on data from 1999/2000) (39) and perhaps 100,000 individuals, and has probably declined by c. 20% over past c. 60 years (6). Estimated total of 2310 pairs in Argentina (1990–1995, increasing to 2600 pairs in early 2000s) (40, 41), 8755 pairs in South Orkney Is (where numbers probably fluctuating, e.g. on Laurie I) (33, 42), 6185 pairs in South Shetland Is, and increasing overall on Antarctic Peninsula (43) (albeit numbers in N of peninsula are decreasing) (44), but was declining on South Georgia (45), where most recent (2007) estimate was of 8700 pairs (46). Other significant populations include 3600 pairs on Heard I and 2000–2200 pairs on Macquarie I (47). Widespread, increasing in a few places (e.g. Prince Edward I (48), and on Possession I, Crozets) (49, 25), fluctuating in others (e.g. Marion I, where numbers currently falling) (44, 50, 51), but has severely declined or disappeared from some sites now much frequented by man, e.g. colony at Pointe Géologie (Adelie Land) down from 69 pairs in 1956 to 14 pairs in 1984, due to proximity of French base and associated disturbance, and numbers in this region declined a further c. 4% between 1985 and 1999 (52); recent decline of at least 55% in Australian Antarctic Territory, where population most recently estimated at 197 pairs (47). Falkland Is formerly held c. 3200 pairs, when some still shot and eggs destroyed each year, as birds alleged to kill lambs, but population most recently (2004/05) estimated at 19,529 pairs (range 18,420–20,377 pairs) at 38 localities (53). Fewer than 250 pairs on Gough I, in 2000/01, where species has apparently increased since 1979 (54). Only recently discovered breeding in Chubut Province, S Argentina (55). No recent breeding records from Bouvetøya (1). Population of Heard and McDonald Is c. 4500 pairs, but breeding success down by 43% since 1951. Future security of species probably closely linked with that of seal and penguin colonies, which are important source of food while breeding; however, main problems are vulnerability to disturbance and levels of incidental mortality in commercial fisheries, especially for Patagonian toothfish (Dissostichus eleginoides), which was suspected to have accounted for 2000–4000 birds in 1997/98 alone (6). Mitigation techniques have now been devised and tested (56, 57, 58). Contaminants and plastics are also newly-emerging threats to this and other subantarctic seabirds (59, 60).

Distribution of the Southern Giant-Petrel - Range Map
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  • Migration
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Distribution of the Southern Giant-Petrel

Recommended Citation

Carboneras, C., F. Jutglar, and G. M. Kirwan (2020). Southern Giant-Petrel (Macronectes giganteus), version 1.0. In Birds of the World (J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, and E. de Juana, Editors). Cornell Lab of Ornithology, Ithaca, NY, USA. https://doi.org/10.2173/bow.angpet1.01
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