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Swinhoe's Storm-Petrel Hydrobates monorhis Scientific name definitions

Carles Carboneras, Francesc Jutglar, Eduardo de Juana, and Guy M. Kirwan
Version: 1.1 — Published August 18, 2021

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Field Identification

18–20 cm (1); 25·6–53·5 g (2); wingspan 44–50 cm (1). Medium-sized dark brownish storm-petrel with notched tail  , small head  , and some white shafts at base of primaries. Dark sooty-brown to dark grey-brown plumage, often greyer on head and neck  , paler on upperwing panel  across outer and central median coverts, all greater coverts and tips of tertials; this panel is not small but often weakly defined  ; white shafts at base of 5–6 outer primaries visible on upperwing at close range; iris dark brown; bill black; legs and feet black. Sexes alike, female averages slightly larger in wing and tail measurements but differences not statistically significant (2). Juvenile similar to adult, but will be in fresh plumage during boreal autumn/winter when adult heavily worn or in wing moult (1). Slightly smaller and smaller-headed than H. markhami and H. melania, tail notched rather than forked, while head often looks greyer rather than blacker compared to body colour; differs from H. tristrami and apparently dark-rumped individuals of H. leucorhous in smaller head, slimmer general appearance , notched rather than forked tail  , narrower wing with often less contrasting bar on its upper surface (though latter character variable) usually not reaching to bend of wing, at close range also by pale shafts at exposed bases of outer five (or six) primaries, and from former also by smaller size.

Systematics History

Perhaps separable in genus Cymochorea, along with H. leucorhous, H. tristrami and H. markhami (3, 4). Sometimes considered a race of H. leucorhous; the two may be closely related to H. homochroa. Monotypic.

Subspecies

Monotypic.

Distribution

Tropical Indian and W Pacific Oceans: breeds from Japan (islets off Kyushu and Honshu) W to Yellow Sea off China and Korea, and N to extreme SE Russia. Recent records suggest possible breeding in N Atlantic.

Habitat

Marine and normally pelagic, but also occurs in coastal waters. Breeds on small offshore islands, on Kutsujima Is, Japan, within evergreen forest dominated by Machilus thunbergii, with Camellia japonica and Ilex integra trees (5); off Korea, vegetation on breeding islands is typically dominated by Carex boottiana (2).

Movement

Migrates S & W to winter in N Indian Ocean (W to off Somalia) and Arabian Sea; irregular in Red Sea, straggling N to Eilat in Gulf of Aqaba (Jan 1958, Sept 2001, Apr 2003, Sept 2016) (6, 7, 8). Recorded off Oman between late May and late Dec, usually in small numbers, but once c. 100 (Nov 1997) following a cyclone (9). Off SW India, records (not all of them confirmed) are available from most months, mainly Mar–Oct (10, 11). Commonest storm-petrel in Strait of Malacca (12), where pronounced eastbound passage observed in Sept–Oct, westbound in Apr–May (13, 14) (exceptionally until late Jun) (15), with large numbers recently confirmed moving through neighbouring Singapore Strait in Sept–Nov and May (exceptionally mid Jun), including single-day maxima of 510 and 470 in mid Sept (16), and has been claimed as far E as between Ambon and Buru (Sept) (17) and Tayandu Is (Aug), Maluku (Indonesia) (18), as well as between Tanahjampea and Pantar, at S edge of Banda Sea (Oct) (19). Single unaccepted record off SE Alaska in Aug 2003 (20) and one definite record in the Philippines (off Palawan, May 2013) (21). Occurrences in NE Atlantic  , where first identified in 1983 (although an 1829 Madeira record is sometimes attributed to this species) (22) and genetic and vocal analyses were used to confirm identity of some birds on caught on land (23, 24), now widely assumed to indicate presence of (presumably) tiny breeding population there, rather than being vagrants from Pacific breeding colonies that had entered the Atlantic via Cape of Good Hope (as was originally postulated) (25) or crossed from the Red Sea to Mediterranean overland (26); some NW European records of dark-rumped storm-petrels that have been suggested to have involved present species subject to considerable controversy, most notably a bird off SW England in Aug 1988, which has been variously attributed to present species, H. tristrami, H. matsudairae or even Bulwer’s Petrel (Bulweria bulwerii) (22, 27, 28, 29). Northernmost European records on Fair Isle (Scotland), in Aug 2013 (30). Recently (since 1993) also recorded four times off E North America (Jun to mid Aug), during pelagic trips from Cape Hatteras, North Carolina (31, 20), and there are possible records of this species from as far S as off Mauritania (Jan 1990) (32).

Diet and Foraging

No information available on diet. Feeds mainly on wing by dipping; does not patter. In Maldives, has been observed scavenging in company of feeding pod of false killer whales (Pseudorca crassidens) (33).

Sounds and Vocal Behavior

Two main vocalizations, a purring call given from within burrow (and presumably also ground), which is given only by males (very similar to that of H. tristrami) (34), and sexually dimorphic chattering call (longer and more complex than in H. leucorhous) (23) given in flight and on ground, in which male sounds cover a broad frequency range whereas females possess clear harmonic structure (35, 12). Studies suggest that it is the harmonic structure of the chattering call, rather than its rhythm, that serves as the cue for sex recognition (35). Silent at sea.

Breeding

Very poorly known. Starts Apr, with egg-laying in May–Jun, sometimes as late as early Jul (12). Forms loose colonies; nests in burrows. Clutch single egg.

Not globally threatened. Currently considerd Near Threatened. Much work required to determine population sizes and trends, main threats and conservation requirements. Global population speculated to perhaps number anything between 30,000 and > 130,000 pairs (12, 5). Largest known colony on Verkhovsky I, S of Vladivostok, with c. 7500–8370 pairs, with c. 100 additional pairs on small nearby islands; substantial predation by crows (Corvus) and migrating owls (Asio), but no mammals; frequent visits by tourists resulted in many nest losses, until protection of island in 1984. Only other known colony off Russia, on Karamzin I, also in Sea of Japan, numbers just 30–40 pairs (12). Minimum 5000 pairs in Japan, on islands off Honshu, Shikoku and Kyushu, including from N to S, Okino-shima (180 pairs), Oki-shoto (unknown numbers), Kutsujima Is (c. 3800 pairs in late 2000s), Hachijo-jima, Izu Is (< 200 pairs), Nanatsu-shima (unconfirmed), Sangan-jima (< 200 pairs), Benten-jima (colony probably extinct) (5), and possibly also in Ryukyu Is (12); little known of populations in China (off Shandong, Guangdong), off Taiwan (36) and off S & W Korean Peninsula, where there is an estimated 7900–11,890 pairs on Chi’lbal I (12) and c. 112,000 pairs on Kugul I (5). Also known to breed on Guguldo Is, off Korea (2). Recent survey for seabirds on islands off Zhejiang coast (China) failed to discover any evidence of the species breeding there (37) and only breeding site off Guangdong harbours only c. 100 pairs (5), but 2500 birds were ringed on Dagong I, off Qingdao, Shandong, during recent surveys; this island is also subject to some tourist pressures (38). In Japan, colony on Koyashima I, Okino-shima, decimated by accidentally introduced brown rats (Rattus norvegicus) and has still to fully recover, despite subsequent removal of the rats (5). Possibly also breeds in NE Atlantic, e.g. on Salvagem Grande (Madeira), where one was trapped each Aug over three consecutive years in 1990s (including once with brood patch) (39), or the Canaries (one caught ashore with a brood patch in 2009) (40), but perhaps also the Azores (where species only recently recorded, Aug 2012) (41) or Cape Verdes (where it is still unknown) (42), and there is also a record (Jul 1994) of one in a colony of H. pelagicus on an islet off Benidorm (Spain) in the Mediterranean (26). Records from Selvagem Grande include two potential pairs found and sound recorded in 2008 at different sites, one of them duetting in a burrow, but capture/recapture patterns suggest that a possible breeding population is small and likely not self-sustaining; moreover, the high haplotypic diversity of the sampled individuals (six during 2007–2013) suggests that most were immigrants (43). 

Distribution of the Swinhoe's Storm-Petrel - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Swinhoe's Storm-Petrel

Recommended Citation

Carboneras, C., F. Jutglar, E. de Juana, and G. M. Kirwan (2021). Swinhoe's Storm-Petrel (Hydrobates monorhis), version 1.1. 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.swspet.01.1
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