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Open AccessJournal ArticleDOI

The genetics of polymorphism in the goose anser caerulescens.

Fred Cooke, +1 more
- 01 Jun 1968 - 
- Vol. 22, Iss: 2, pp 289-300
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TLDR
This paper is an attempt to analyze the genetic basis for the polymorphism in this dimorphic species, by investigating a sample of the large colony at Boas River, Southampton Island, North West Territories, Canada.
Abstract
Although the most recent A.O.U. checklist of North American Birds (1957) records the Blue Goose and the Lesser Snow Goose as distinct species (Chen caerulescens [= Anser caerulescens] and C. hyperborea [= A. hyperborea] respectively), many ornithologists today agree with the conclusion of Cooch (1961) that the smaller subspecies of the Snow Goose Anser caerulescens caerulescens is polymorphic and has two clearly defined color phases, a blue phase and a white phase. Some authors, e.g. Manning et al. (1956) prefer to regard the Blue Goose and the Lesser Snow Goose as conspecific but consisting of two subspecies. Polymorphism is well known in birds and has been well documented by Mayr (1942) and Huxley (1955). In only a few cases, however, has it been possible to infer the genetic basis of the polymorphism. O'Donald and Davis (1959) have studied the genetics of the color phases of the Parasitic Jaeger (Stercorarius parasiticus) . Meyerriecks ( 1957) has some observations on genetics of polymorphism in the Great Blue-Great White Heron complex. Williamson (1957) reported on the genetic basis for the dimorphism found in the goslings of the Ross's Goose, and Ryder (1967) extended these observations. Lowther (1961) recorded an interesting case of polymorphism in the White-throated Sparrow and Thorneycroft (1966) presented cytological evidence for the genetic basis of this polymorphism. Most observers, however, have had either to ignore the genetic basis or to suggest a genetic basis with no genetic evidence on which to base their speculations. Genetic data of this nature are not easy to obtain in non-domesticated birds. Many birds will not breed in captivity. In the wild it is possible to gain meaningful genetic evidence only if a large number of families is studied and if the polymorphism is detectable in nestling stage, or alternatively if the nestling can be kept in captivity, or can be marked for individual recognition until the adult plumage appears. The polymorphism of Anser caerulescens is in many ways ideal for study. Large colonies, where the different morphs interbreed, can be found. The polymorphism is detectable in both adult and gosling plumages and is observable in both sexes. Most species of birds produce too few offspring in anyone season for a genetic study based on individual families to be feasible, but when a large population can be examined, some pooling of data allows conclusions about the genetic basis to be drawn. This paper is an attempt to analyze the genetic basis for the polymorphism in this dimorphic species, by investigating a sample of the large colony at Boas River, Southampton Island, North West Territories, Canada. Although there are indications that color differences lead to differences in choice of nest sites and time of breeding, these attributes of the polymorphism have been ignored in the present study. In the course of this analysis, observations on the assortative mating behavior were made. These observations, which are described in detail below, led to the conclusion that some form of imprinting, as suggested by Huxley (1955), was operating. This in turn suggested that such imprinting, if complete, could lead in a few generations

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Citations
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Journal ArticleDOI

The evolution, maintenance and adaptive function of genetic colour polymorphism in birds.

TL;DR: A review of the current theoretical and empirical knowledge of the evolution, maintenance and adaptive function of colour plumage traits for which the expression is mainly under genetic control shows that genetically inherited morphs can reveal the same qualities.
Journal ArticleDOI

Ecological Significance of Imprinting and Early Learning

TL;DR: A review in a series mainly devoted to the field of ecology of imprinting, where it is being realized more and more that imprinting may also be of considerable ecological and evolutionary significance.
Journal ArticleDOI

Conserved genetic basis of a quantitative plumage trait involved in mate choice

TL;DR: Phylogenetic reconstructions of variant MC1R alleles in geese and skuas show that melanism is a derived trait that evolved in the Pleistocene.
Journal ArticleDOI

The genetic legacy of Mother Goose– phylogeographic patterns of lesser snow goose Chen caerulescens caerulescens maternal lineages

TL;DR: By using the polymerase chain reaction to amplify and sequence 178 bp of a rapidly evolving region of the mtDNA genome (segment I of the control region) from 81 individuals, approximately 11% of the variation present in the lesser snow goose Chen caerulescens caeruleescens L. caerULescens is removed.
Book ChapterDOI

Sexual and Other Long-Term Aspects of Imprinting in Birds and Other Species

TL;DR: The chapter discusses the four main criteria that are the characteristic for imprinting, and discusses the significance of the early determination of sexual preferences for the general concept of imprinting and the biological function and possible evolutionary consequences of sexual imprinting.
References
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Journal ArticleDOI

Chromosomal Polymorphism in the White-Throated Sparrow, Zonotrichia albicollis (Gmelin).

TL;DR: In a study of 35 white-throated sparrows five distinct karyotypes were observed, and a chromosomal polymorphism is present which involves at least two pairs of macrochromosomes.
Journal ArticleDOI

Polymorphism in the white-throated sparrow, zonotrichia albicollis (gmelin)

TL;DR: Mechanisms governing polymorphism are discussed in an attempt to explain the existence of the morphic types in the white-throated sparrow.

Morphism in birds

Julian Huxley
Journal ArticleDOI

Ecological Aspects of the Blue-Snow Goose Complex

Graham Cooch
- 01 Jan 1961 - 
TL;DR: It is believed that the two forms are conspecific and that the species consists of two subspecies: a large form, Chcn cacruIcscens atIantica, which has no color phases, and a smaller form,Chcn caerulescens caeruIescens, which is polymorphic and has two clearly defined color phases.