- Atlantic Petrel
 - Atlantic Petrel
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Atlantic Petrel Pterodroma incerta Scientific name definitions

Carles Carboneras, Francesc Jutglar, and Guy M. Kirwan
Version: 1.0 — Published March 4, 2020
Text last updated June 30, 2019

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Introduction

Often considered to be of doubtful affinities in the years following its description, the Atlantic Petrel is structurally similar to the Great-winged Petrel (Pterodroma macroptera) and the White-headed Petrel (Pterodroma lessonii), but in morphology this gadfly petrel most closely resembles the dark-morph Soft-plumaged Petrel (Pterodroma mollis) and the Herald Petrel (Pterodroma arminjoniana). Appropriately, Atlantic Petrel is only recorded in the Atlantic Ocean, and is restricted as a breeder to the islands of Tristan da Cunha and Gough, with the overwhelming majority of the population confined to the latter. It nests in winter, in burrows and exposed ridges, but there is still very little published breeding data. Worryingly for the species’ conservation, there is evidence of predation by House Mice on this petrel’s chicks. Considered of no conservation concern just a decade ago, the recent data from Gough of very low breeding success have led BirdLife International to currently list the species as Endangered, with a precautionary note that the Atlantic Petrel might warrant upgrading to the highest conservation priority, Critically Endangered, in the near future. Atlantic Petrel probably feeds mainly on squid, of which some may be captured underwater, although smaller percentages of fish and crustacea are also taken. In the Neotropics, this species is known solely from southern Brazil, where it has been recorded mainly in the austral spring, largely in the post-breeding season.

Field Identification

40–43 cm; 420–720 g (1) (exceptionally 310 g) (2); wingspan 104 cm. Only petrel of its size that is all dark with white lower breast and belly ; undertail-coverts dark. White abdomen , otherwise plumage dark brown, including hood , vent and undertail-coverts , blacker patch around eye; bases of primaries paler and greyer, but contrast is rather slight; in worn plumage looks paler and greyer, especially on hood, with paler, whitish throat, and more contrasting dark facial patch; iris very dark brown; bill black; legs pale fleshy pink with blackish-grey distal portion of toes. Sexes alike. Juvenile has greyish tips to mantle feathers in fresh plumage. Other dark petrels with white abdomen sharing similar range have either contrasting whitish markings on underwing (P. mollis) or white wing flashes in upperwing (P. neglecta (3) and pale-morph P. arminjoniana, which is also smaller, with different wing shape, more elongated tail, more dynamic flight action and can show some white on underwing) (3), preventing confusion; furthermore, P. incerta may flap its wings at top of glides, unlike most other Pterodroma (4), and P. neglecta has a fuller, more rounded head and thicker, shorter neck, relatively short and stubby bill, and shorter and broader tail (3).

Systematics History

Genetic data indicate that this species forms a clade with P. magentae, P. lessonii, P. macroptera and P. gouldi (5); also, feather lice shared with these taxa (6). Sometimes considered sister-species of P. lessonii. Monotypic.

Subspecies

Monotypic.

Distribution

S Atlantic Ocean, breeding at Gough I; formerly bred at Tristan da Cunha, where possibly now extinct (7).

Habitat

Marine and probably pelagic . Breeds on oceanic islands, occupying ridges at altitudes of 50–600 m, mainly below 300 m on Gough, where burrows are exclusively located in coastal tussock and fernbush habitats (1).

Movement

Disperses throughout S Atlantic , occurring off E coast of S America and rounding South Africa into Indian Ocean (mainly in Jun–Dec) (8), with records spread far and wide, reaching NW to Eilat, Israel/Jordan (May 1982, Apr 1989) (9), E to Australia  , off W Victoria (Feb 2005) (10) and perhaps also N to Indian waters, off the Chagos archipelago and between Cape Comorin and the Maldive Ridge (the latter in Jun 1985) (11). In Atlantic, off E South America is generally found N to at least 20° S, and S to 56º S (being most abundant at 42–46º S) (12), while in C Atlantic most frequently occurs at 33–50º S, but in SE Atlantic is generally recorded in small numbers at latitudes of 12–48º S (8). Small numbers reach South Georgia (53º S) (13), the Drake Passage (56–59° S) and even occasionally Antarctic waters, e.g. at the South Shetland Is, with a record of five together in Weddell Sea (below 65º S) in Jan 1990 (12). A remarkable inland record from Europe—a bird found dead in what is now the Slovak Repubic in 1870 (14)—is now not generally accepted (11) given that its provenance is uncertain and unclear (15); the specimen, which is no longer extant, was originally identified as P. hasitata (14). In South America, three emaciated birds were collected at a hydroelectric power dam in Pará (E Amazonian Brazil) in Sept 1984 (03º50’ S, 49º45’ W), 400 km from the nearest open sea and > 2000 km from the species’ usual range in the W Atlantic (16).

Diet and Foraging

Mostly cephalopods (especially gonatid, onychoteuthid and histioteuthid squid) (17), with some mesopelagic fish (notably myctophids) (17) and crustaceans (e.g., Euphausiacea, Hyperiidea, Natantia) (17). Studies have revealed that squid forms 70% or 87% (by weight) of diet (species include Argonauta argo, Brachioteuthis sp., Chiroteuthis sp., Discoteuthis discus, Gonatus antarcticus, Histioteuthis sp., H. atlantica, H. meleagroteuthis, Onychoteuthis ?banksi, Taonius sp., Todarodes sp.) (17), with 11% or 17% comprising fish (species include Diaphus sp., Gymnoscopelus piabilis, Lampanyctus australis, Melamphaes simus, Melanonus sp., Borostomias ?mononema) (17) and 13% or just 1% crustacea (17). Squid prey up to 54 cm and 234 g in mass have been recorded (17). Prey taken generally by surface seizing, but it has been suggested that some may be taken underwater (4). Generally appears to forage alone or in monospecific flocks, rather than joining mixed-species feeding frenzies (12).

Sounds and Vocal Behavior

Considered similar to that of P. macroptera (4).

Breeding

Breeds in winter, returning to colonies for courtship and burrow renovation in late Mar to late Apr (1), then depart on pre-laying exodus for a minimum of c. 50 days (1), with egg laying in mid Jun–Jul, hatching mid Aug to mid Sept (1), and late fledglings may depart only in Jan (4). Exclusively nocturnal on land (1). Colonial; nests in burrows dug in soft soil. Clutch single white egg, mean size 68·9 mm × 49·8 mm (1); incubation c. 55 days (1); chicks have brown-grey down; fledging about 138 days (one of the longest periods of any Pterodroma), gaining mass at rate of just c. 4 g/day (1). Nothing is known of age of first breeding, breeding frequency or survival. Current breeding success on Gough is very low (based on sample data from 2001 and 2004), with just 20% of eggs producing fledged young and most losses occurring during chick-rearing period (fledging success was 35% versus hatching success of 57%), and in 2007, from 58 nests sampled just one chick fledged (18); main predators of fledglings appear to be house mice (Mus musculus) (1).

ENDANGERED. Previously considered Vulnerable. Present population numbers perhaps a few hundred breeding pairs at Tristan da Cunha (although recent evidence of breeding is unavailable) (19) and perhaps 1,790,000 pairs (1) at Gough I; BirdLife International considers that the overall population might number five million birds. Apparently absent from Nightingale and Inaccessible Is, in Tristan group, although survey work during the winter breeding season is limited. At Tristan, suffered extreme human exploitation prior to the 1940s, especially as other food was scarce in winter, by which time P. incerta was very rare there, but is unlikely to suffer much harvesting now; several introduced predators, including rats and previously cats (which were eradicated in 1970s). On Gough I, house mouse (Mus musculus) is only introduced predator (but is extremely abundant) (1), and has recently been confirmed to be main predator of chicks (including healthy individuals) of this petrel and other seabirds, including albatrosses (Diomedea exulans) (20) and Ardenna gravis—data from the breeding seasons between 2003 and 2008 indicate that mean daily survival rate of eggs is 0·998, hatching success through entire incubation period 0·924 and daily chick survival rates 0·990, which gave modelled fledging success of 0·247 and mean annual breeding success (chicks fledged per breeding attempt) of 0·228 (a low figure compared to congeners, but is perhaps far too optimistic given finding that just one chick fledged from sample of 58 nests in one season) (18). Burrow occupany rates (based on chicks) are also low, averaging 26% over three seasons (2000, 2001 and 2010), with estimates of chick survival in same years varying from 36% to 69% (mean 49%) and house mice predation the apparent principal cause of mortality (21). In addition, population of 6000–8000 skuas (Catharacta antarctica) on Gough feed almost entirely on seabirds, including the present species. Night strikes (the birds having been attracted to lights) have been ameliorated at Gough meteorological station, but may still pose a problem on ships. Freak events may also cause heavy mortality, e.g. by Hurricane Catarina in Mar 2004, wherein 354 birds were recorded blown up to 420 km inland (and to altitudes of 1100 m above sea level) across the S Brazilian states of Rio Grande do Sul and Santa Catarina, all in heavy moult and near starvation, with the larger numbers of females recorded thought to be due to difference in at-sea distribution or in body condition (2); one analysis of occasional carcasses washed-up on S Brazilian beaches revealed no evidence of susceptibility to range of threats that affect so many other seabirds (oil pollution, ingestion of plastic materials, etc.) (22). Thorough census needed, as well as study of biology and ecology, to establish conservation requirements.

Distribution of the Atlantic Petrel - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Atlantic Petrel

Recommended Citation

Carboneras, C., F. Jutglar, and G. M. Kirwan (2020). Atlantic Petrel (Pterodroma incerta), 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.atlpet1.01
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