Seabird Group Seabird Group

Identifying giant petrels, Macronectes giganteus and M. halli, in the field and in the hand

Carlos, C. J.1,2*, & Voisin, J.-F.3

https://doi.org/10.61350/sbj.21.1

1 Laboratório de Elasmobrânquios e Aves Marinhas, Departamento de Oceanografia, Fundação Universidade Federal do Rio Grande, CP 474, 96201-900, Rio Grande, RS, Brazil

2 Current address: Rua Mário Damiani Panatta 680, Cinqüentenário, 95013-290, Caxias do Sul, RS, Brazil

3 USM 305, Département Ecologie et Gestion de la Biodiversité, Muséum National d’Histoire Naturelle, CP 51, 57 rue Cuvier, F-75 005 Paris, France

Full paper

Abstract

The two similar-looking species of giant petrels, the Northern Giant Petrel Macronectes halli and the Southern Giant Petrel M. giganteus, are renowned for being difficult to identify. In this paper we review and offer new guidelines on identification of these birds at sea, on land, and as dead specimens. Criteria for identifying giant petrels are available in the scientific literature, especially regarding bill-tip coloration which readily differ from one species to another. Plumage characters, although useful to discriminate species, are not adequately covered at present. Thus, for each species we describe in detail and illustrate distinctive age-related plumage stages, or types, from juveniles through to adult breeders. We also comment on giant petrel biometrics, body weight, and some aspects of their behaviour, in order to help ornithologists and birdwatchers separate males and females, and eventually specimens from South America–Gough Island, Antarctic and sub-Antarctic regions.

Introduction

Giant petrels Macronectes are large Procellariiformes with a wingspan usually in excess of two meters in males, slightly less in females, and are similar in size to Thalassarche mollymawks. They display a wide range of plumages, from dull-black to brownish-grey and even white, according to age and species. The discovery of two distinct populations breeding at Macquarie Island (Australian Antarctic Territory; Figure 1), laying about six weeks apart (Warham 1962), led Bourne & Warham (1966) to restrict the name Macronectes giganteus (Gmelin, 1789) to those birds breeding on Antarctic islands, the Antarctic Peninsula and continent, and on islands of the South Atlantic, and to resurrect the name Macronectes halli Mathews, 1912 for birds breeding on sub- Antarctic islands, from South Georgia through the Indian Ocean to the New Zealand area. Voisin & Bester (1981) and Voisin (1982b) showed later that the form breeding on the Falkland and Gough Islands (South Atlantic), as well as on islands off the Argentine coast, represented a well-marked subspecies: acronectes giganteus solanderi Mathews, 1912, for which Carlos et al. (2005) proposed the vernacular name South Atlantic Giant Petrel. Hereafter, we follow current usage in referring to M. halli as Northern Giant Petrel and M. giganteus as Southern Giant Petrel.

Ringing recoveries and subsequent satellite-tracking studies have shown that both species of giant petrel roam the southern ocean widely, especially immatures, but also adults in the breeding and non-breeding seasons (Hunter 1984; Voisin 1990; Parmalee 1992; Trivelpiece & Trivelpiece 1998; González-Solís et al. 2000a, b; Patterson & Hunter 2000; Patterson & Fraser 2000, 2003; BirdLife International 2004; González-Solís et al. 2008). Antarctic populations of Southern Giant Petrel are especially wide-ranging, and one should not assume that, for example, a Southern Giant Petrel seen off the Argentinean–Brazilian coast at any time of the year is necessarily M. g. solanderi.<>

Recently, Penhallurick & Wink (2004) proposed to re-group M. halli as a subspecies of M. giganteus on the basis of low mitochondrial cytochrome-b gene divergence. Such a position is untenable since both species have long bred sympatrically, and often in close proximity, on South Georgia, Marion, Crozet and Macquarie Islands (Figure 1) without regular interbreeding. A few cases of inter-specific breeding involving male M. giganteus paired to female M. halli have been reported from Marion (Burger 1978; Cooper et al. 2001) and Macquarie Islands (Johnstone 1978), although the resulting eggs did not hatch. Only at South Georgia has occasional hybridisation been reported (Hunter 1982, 1987). Given these circumstances, we can reasonably assume that gene flow between the two species is extremely limited. In birds, many closely related species are known to hybridise regularly, e.g. Anas dabbling ducks (Carboneras 1992), and Common Phylloscopus collybita and Iberian P. ibericus Chiffchaffs (Salomon et al. 2003), without merging into one single species. Even if ‘their apparent failure to interbreed is not quite as straightforward as if they bred at the same time without interbreeding’ (Penhallurick & Wink 2004), M. giganteus and M. halli do not genetically mix.

Several authors have dealt with giant petrel identification, especially of birds at sea (Johnstone 1971, 1974; Conroy et al. 1975; Voisin 1982a; Hunter 1983; Voisin & Teixeira 1998; Jiguet 2000; Shirihai & Jarrett 2002). Here we review, and offer new guidelines on, giant petrel identification at sea, on land, and as dead specimens.

Acknowledgements

We are grateful to Steve Copsey, Fernanda I. Colabuono and Ronald Saldino for allowing us to use their photographs. Renata F. Cunha kindly prepared Figures 7 & 8. CJC received support from Fundação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brazil. The typescript benefited from the input of Bernie Zonfrillo, Stephen Hunter, Bill Fraser, an anonymous referee and the editorial advice of Martin Heubeck.

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