The Greenland White-fronted Goose Anser albifrons flavirostris
The Greenland White-fronted Goose Anser albifrons flavirostris
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