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The Greenland White-fronted Goose Anser albifrons flavirostris

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2Limits to population size in recent historical times<br />

2.1 Current taxonomic status<br />

<strong>The</strong> Greater <strong>White</strong>-<strong>fronted</strong> <strong>Goose</strong> <strong>Anser</strong> <strong>albifrons</strong><br />

is one of the most widely distributed large waterfowl<br />

species in the arctic (Ploeger 1968, Ely &<br />

Dzubin 1994). Four forms are currently recognised<br />

as sub-species around the arctic region (see Figure<br />

2.1 and discussion below).<br />

Coburn (1902) was the first to suggest that the<br />

<strong>White</strong>-<strong>fronted</strong> Geese in western Ireland more resembled<br />

those that wintered in North America<br />

than those in Europe. Nevertheless, it was as recently<br />

as 1947 that Christopher Dalgety and Peter<br />

Scott first described the <strong>White</strong>-<strong>fronted</strong> Geese<br />

wintering in Ireland, Scotland and Wales as a new<br />

race distinct from the European <strong>White</strong>-<strong>fronted</strong><br />

<strong>Goose</strong> <strong>Anser</strong> a. <strong>albifrons</strong>. <strong>The</strong> new subspecies they<br />

named the <strong>Greenland</strong> <strong>White</strong>-<strong>fronted</strong> <strong>Goose</strong> <strong>Anser</strong><br />

<strong>albifrons</strong> <strong>flavirostris</strong> (Dalgety & Scott 1948). This<br />

Figure 2.1. Breeding distribution of currently recognised <strong>White</strong>-<strong>fronted</strong> <strong>Goose</strong><br />

subspecies, <strong>flavirostris</strong> (<strong>Greenland</strong>), frontalis (Nearctic and Eastern Palearctic),<br />

gambelli (Alaska) and <strong>albifrons</strong> (Palearctic), based on Cramp & Simmons (1977)<br />

and Ely & Dzubin (1994).<br />

form is one morphologically distinct group from<br />

the circumpolar distribution, which extends from<br />

the central Canadian arctic (west of Hudson Bay)<br />

through to Alaska, and from the far east of Russia<br />

to the Kanin peninsula (Figure 2.1).<br />

Although there remains considerable discussion<br />

about the precise taxonomic relationships, most<br />

authorities agree that the breeding range of the<br />

nominate race extends from the Kanin peninsula<br />

to the Kolyma river in tundra Russia (Cramp &<br />

Simmons 1977, Mooij et al. 1999). To the east of<br />

this, it is replaced by frontalis in Russia, which<br />

winters in the eastern Palearctic. This sub-species<br />

also breeds across North America and winters in<br />

Mexico and along Gulf and Pacific coasts (Ely &<br />

Dzubin 1994). However, intensive studies from<br />

the Pacific flyway show that allopatric Alaskan<br />

breeding groups maintain temporal separation on<br />

staging and wintering areas which has probably<br />

contributed to the evolution<br />

of previously described<br />

phenotypic differences between<br />

these populations<br />

(Orthmeyer et al. 1995, Ely<br />

& Takekawa 1996). <strong>The</strong>se<br />

authors suggest that these<br />

sub-populations, along with<br />

the Tule <strong>White</strong>-<strong>fronted</strong><br />

<strong>Goose</strong> (A. a. gambelli which<br />

breeds in Cook Inlet, Alaska<br />

in the taiga zone and winters<br />

in Oregon and California),<br />

may represent part of<br />

a 'Rassenkreis', a group of<br />

subspecies connected by<br />

clines. Such a situation is<br />

maintained over time<br />

through limited but regular<br />

genetic exchange between<br />

units otherwise segregated<br />

in time and space. Hence,<br />

the internal genetic uniformity<br />

of the existing taxonomic<br />

units is unlikely to be<br />

as simple as the current<br />

sub-species structure might<br />

suggest. Nevertheless, in<br />

this respect, <strong>flavirostris</strong> remains<br />

amongst the most<br />

geographically isolated<br />

17

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