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Flesh-footed Shearwater Ardenna carneipes Scientific name definitions

Carles Carboneras, Francesc Jutglar, Guy M. Kirwan, and Christopher J. Sharpe
Version: 1.0 — Published March 4, 2020
Text last updated April 24, 2017

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Introduction

This large, dark shearwater barely reaches Neotropical offshore waters, occurring rarely during migration and winter off northwest Mexico, and strictly as a vagrant elsewhere in the region. It breeds on islands in the southern Indian Ocean and southwest Pacific, ranging regularly into the northeast Pacific from Alaska through central California, becoming notably rare south of there. Distinguished with caution from Sooty Shearwater by larger size, slower wingbeats, entirely dark underwing coverts, and pinkish bill with dark tip. Beware confusion with dark extreme Pink-footed Shearwater, which shares similar size, shape, and flight style.

Field Identification

40–48 cm (1); 533–765 g (2); wingspan 99–116 cm (1). Large, broad-winged, entirely dark shearwater with relatively robust pale bill . Plumage blackish-brown overall, usually darkest on head  and neck and on upper surface of remiges and tail, browner fringes on mantle to uppertail-coverts may afford a scaly appearance, especially on scapulars; slightly paler and greyer on underside of remiges  and greater coverts, usually more noticeable at primary bases, which may appear more or less silvery in some lights; abdomen can look obscurely spotted and slightly paler than upperparts; iris blackish ; bill pinkish to pale horn with tip  mostly dusky to black; legs  pink or pinkish  , sometimes with dusky gray wash over part of toes. Sexes alike, but male significantly larger in most measurements (2, 3). Juvenile as adult, but has fresh plumage in Apr–Jul when older birds are worn or moulting (1). Those breeding in E Australia and New Zealand average larger than those in Western Australia (1). Very much resembles A. creatopus, but dark abdomen prevents confusion; structurally more similar to Calonectris shearwaters than to most other Ardenna, while all-dark plumage recalls some Procellaria, but is smaller and has slimmer bill; separated from all-dark Pterodroma by structure, slimmer and paler bill, and flight action; dark-morph Ardenna pacifica is similar in color but has a notably longer, wedge-shaped tail and thinner bill; Puffinus nativitatis is smaller and slender-billed; other dark Ardenna have thinner bills and variable whitish on underwing.

Systematics History

Sometimes considered conspecific with A. creatopus; the two are probably closely related to A. gravis. Birds from Lord Howe I and New Zealand may merit separation as race hulliana, on grounds of different migratory routes and slight size differences. Monotypic.

Subspecies

Monotypic.

Distribution

Indian and Pacific Oceans, breeding on St Paul I (S Indian Ocean) and SW Australia, with single isolated colony in South Australia; breeds also on Lord Howe I (off E Australia) and on islands off North I and in Cook Strait (New Zealand).

Habitat

Marine and pelagic; mainly in offshore waters over continental shelf. Breeds on vegetated (scrub- or forest-covered) hills or grassy slopes facing sea.

Movement

Migratory. Ringing results show that birds from Lord Howe I move N to winter off E Korea mainly Apr–Jul, but from late Mar and until Sept (2, 4); New Zealand population was assumed to follow same pattern, although all ringing recoveries have been from within 645 km of colonies, and routes are poorly known, e.g. is rare off New Guinea (5) and in Melanesian seas (6); species occurs N to Sea of Okhotsk (Jun) (2). Data loggers were recently sused to study the migration of three shearwaters that bred in New Zealand; in early April, they migrated to the NW Pacific Ocean in 23 ± 2 days, occupying core distributions within the Kuroshio/Oyashio transition system for 91 ± 17 days, with subsequent movements into the Sea of Okhotsk prior to return migration to New Zealand in mid Sept (19 ± 1 days) (7). Also recorded in small (but increasing) numbers off North America (Gulf of Alaska and British Columbia S to Baja California), especially in warm-water years, mainly May–Nov, most numerous between Sept and Nov, but reported off NW Mexico between Jan and Jul (mainly Mar–May) and recorded all months off C & S California, with occasional records N to Washington in Dec–Mar (2, 1). Two specimen records from Chile, off Valdivia (Oct 1913) and Robinson Crusoe I (Feb 1914), but sight records off C Chile in Sept seem doubtful (8, 9). Migration through NE Pacific may follow clockwise pattern (1). Another population, the W breeders (in Australia), winters in Indian Ocean, mostly in Arabian Sea, where arrives in late May and is commonest between late Jun and mid Aug (2) (present off Oman Apr to mid Nov, sometimes in very large numbers) (10, 11), some birds occurring SW to South Africa and Mascarenes (12), passing through S Indian Ocean in mid to late Apr and returning in Sept (2), and has exceptionally been recorded NW to head of Red Sea at Eilat (Israel/Jordan, Aug 1980) (13, 14) and on W coast of India (Kerala) (15). On departure from breeding colonies, birds initially appear to move N towards W Indonesia, before heading W across Indian Ocean (16). Record of large numbers in Indonesia suggests at least some of W breeders may winter in Pacific.

Diet and Foraging

Little known; squid and fish recorded, and these are probably chief dietary constituents, at least during breeding season, but evidence from stable isotope studies suggests that species also takes significant numbers of soft-bodied, non-cephalopod invertebrates (e.g. coelenterates) during non-breeding season, when lanternfish (Myctophidae) and Pacific saury (Cololabis saira) were the principal prey found in the species’ digestive tracts, while pieces of unidentified fish, possibly Pacific pomfret (Brama japonica) and shredded squid tissue, mostly neon flying squid (Ommastrephes bartrami) were also found (17). Prey  mostly caught by pursuit-plunging; also uses surface-seizing, contact-dipping (18) and diving  (regularly reaching up to 5 m below surface during breeding season) (18). Diving depths during migration (2·5 ± 2·4 m), and in NW Pacific (2·4 ± 2·6 m) were shallower than at onset of breeding (4·8 ± 8·7 m) (7). Forms loose flocks, which may forage with other shearwaters (1). Regularly scavenges behind fishing boats, taking offal, but attracted to other boats only briefly (2, 1). Mostly diurnal feeder .

Sounds and Vocal Behavior

Principally vocalizes at night, from within burrows, on ground or in flight, but occasionally by day (when in nests) at least in response to playback; an introductory “gug-gug-gug” followed by a trisyllabic crooning “ku-kooo-ah” that may be repeated 3–6 times, followed by a dying splutter, and the whole lasting c. 10 seconds (2).

Breeding

Starts late Sept/early Oct with return to colony, egg-laying c. 21 Nov to 12 Dec and fledging late Apr/early May (2). Strictly nocturnal at breeding sites, arriving c. 30 minutes after sunset (2). Colonial, using same burrows as winter-breeding Pterodroma macroptera (2); nests  in burrows   1–2 m long (2). Single white egg  , size 60–75 mm × 38–50 mm (2); incubation (estimated) c. 53 days, with mean shift length of 9·5 days on Lord Howe I (19); chicks  have grey down  , brooded for 2–3 days, thereafter fed every 0·9 days, with meal size increasing (but frequency of feeds decreasing) as fledging period progresses and overall mean meal size 112 g (2, 19); fledging c. 92/93 days when c. 545 g, but reaches peak weight of c. 882 g when 60 days old (2) or 1160 g (or 193% of mean adult body mass) at 53 days old, according to different Australian studies (19). During chick-rearing period, birds from Western Australian colonies generally fed within 300 km of nest-sites (16), while at Lord Howe I foraging-trip duration was bimodal, with both short trips (≤ 3 days) and long trips (> 3 days) recorded, with mean trip length increasing during the late chick-rearing period (19). Few additional data, but longevity record an Australian bird that was in excess of 30 years old (2) and breeding success on Lord Howe I, Australia, in 2002 was estimated at 50% (20).

Not globally threatened. Currently considered Near Threatened. Previously thought to number several hundred thousand birds, perhaps 220,000 pairs and 650,000 individuals (2). However, errors have been found in hitorical literature, and, together with more recent surveys, global population recently recalculated at no more than 74,000 breeding pairs (21). Overall, Australian population estimated at 125,000–350,000 pairs (> 80% of global population) in early 2000s (22). Lord Howe I held an estimated c. 20,000–40,000 breeding pairs in 1978 (2), revised to 17,462 breeding pairs in 2003, when burrow occupancy was calculated at 58% (20); more recently, in 2009, population was estimated to be 16,267 pairs, representing a decline in the number of pairs since the previous count of 6·8% (c. 1·3% per year) (23). Sandy I historical surveys in 1976 corrected to 5011 pairs had declined to 3400 pairs in 2012 (21). 500 pairs on St Paul I (2). Perhaps 10–15 pairs on Phillip I, in Norfolk group (where breeding not yet confirmed) (24). In New Zealand, 50,000–100,000 pairs estimated in 1983, 25,000–50,000 pairs in 2000, on c. 20 islands off North I S to Cook Strait (most important colonies being on Lady Alice, Whatupuke, Coppermine and Karewa) (2). Recent surveys suggest the population is significantly smaller at 10,000–15,000 pairs BirdLife International (2017) Species factsheet: Ardenna carneipes. Downloaded from http://www.birdlife.org on 24/04/2017. . New Zealand population has most recently been assessed as At Risk and to be declining (25); adult survival, however, is moderate to high in N New Zealand compared to that of congeners (26). Main threat is rate of destruction of natural breeding habitat, dense forest on low flat ground or gentle slopes on offshore islands (e.g., increasing urbanization has reduced available on Lord Howe I by > 35% since 1978) (20); birds now being displaced to higher ground. Species is known to be taken as bycatch by longline fisheries, but generally impacts are poorly studied and perhaps under-estimated (27, 28, 2, 29), except for the Lord Howe I population, for which the mean number of birds killed between 1998 and 2002 was estimated to be 1794–4486 birds per year, equating to between 8972 and 18,490 birds over this five-year period (30). Tourism also contributes to local destruction of coastal sites. Suffers some predation by rats (Rattus norvegicus) (2), cats, skinks, foxes and in past pigs; some human exploitation in past, and species was formerly more widespread in New Zealand (2). Maintenance of present numbers would be favoured by creation of reserves on offshore islands, with human access restricted; eradication of introduced predators also desirable.

Distribution of the Flesh-footed Shearwater - Range Map
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  • Migration
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Distribution of the Flesh-footed Shearwater

Recommended Citation

Carboneras, C., F. Jutglar, G. M. Kirwan, and C. J. Sharpe (2020). Flesh-footed Shearwater (Ardenna carneipes), 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.flfshe.01
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