Forage Quality in Brood Rearing Areas of the Lesser Snow Goose and the Growth of Captive Goslings

1995 ◽  
Vol 32 (2) ◽  
pp. 276 ◽  
Author(s):  
F. L. Gadallah ◽  
R. L. Jefferies
2017 ◽  
Vol 81 (5) ◽  
pp. 846-857 ◽  
Author(s):  
Jerry W. Hupp ◽  
David H. Ward ◽  
Kyle R. Hogrefe ◽  
James S. Sedinger ◽  
Philip D. Martin ◽  
...  

Nature ◽  
1987 ◽  
Vol 326 (6111) ◽  
pp. 392-394 ◽  
Author(s):  
Thomas W. Quinn ◽  
James S. Quinn ◽  
Fred Cooke ◽  
Bradley N. White

The Auk ◽  
1931 ◽  
Vol 48 (3) ◽  
pp. 335-364 ◽  
Author(s):  
George Miksch Sutton

1996 ◽  
Vol 74 (5) ◽  
pp. 965-969 ◽  
Author(s):  
Barbara Ganter ◽  
Fred Cooke ◽  
Pierre Mineau

Vegetation in a small section of nesting habitat in a Lesser Snow Goose colony was mapped in 1976 and again in 1993. During the 17-year period, ground cover changed dramatically from being dominated by salt-marsh graminoids and short grasses to being dominated by willows and areas of bare sediment. Lyme grass, Elymus arenarius, a plant strongly favoured by Snow Geese when selecting their nest sites, which covered 15% of the ground in 1976, had completely disappeared by 1993. Although the area had contained 79 Snow Goose nests in 1976, no nests remained in 1993. Degradation of the nesting habitat is caused by foraging activities of the geese themselves during the prenesting and nesting phase: salt-marsh graminoids and short grasses are removed by grubbing and the sediment is exposed; E. arenarius plants are removed by shoot pulling. Both clutch size and hatching success can be negatively affected by the decline in available food plants, and, presumably as a consequence, the area was abandoned by breeding geese. This habitat destruction and subsequent abandonment of nesting areas by breeding geese is a process similar to that documented for brood-rearing areas of Lesser Snow Geese.


The Auk ◽  
1916 ◽  
Vol 33 (2) ◽  
pp. 197-198
Author(s):  
Charles W. Townsend
Keyword(s):  

The Condor ◽  
2002 ◽  
Vol 104 (2) ◽  
pp. 432-436 ◽  
Author(s):  
Jason D. Weckstein ◽  
Alan D. Afton ◽  
Robert M. Zink ◽  
Ray T. Alisauskas

AbstractWe reanalyzed Quinn's (1992) mtDNA control region data set including new sequences from nine Lesser Snow Geese (Chen caerulescens caerulescens) and 10 Ross's Geese (Chen rossi) and found the same divergent lineages that Quinn (1992) attributed to vicariant separation of Lesser Snow Goose populations during the Pleistocene. However, peculiar patterns of mtDNA control region sequence variation, including a multimodal mismatch distribution of mtDNA sequences with two levels of population structuring and the sharing of two divergent haplotype lineages, are consistent with two hybridization episodes in Chen geese. Comparisons of mtDNA variation with historical and allozyme data sets compiled by Cooke et al. (1988) are consistent with the hypothesis that sharing of two mtDNA haplotype lineages between Ross's Goose and Lesser Snow Goose resulted from hybridization (Avise et al. 1992). Furthermore, population structure found within one haplotype cluster is consistent with Cooke et al.‘s (1988) hypothesis of past allopatry between blue and white Lesser Snow Geese.Hibridización y Subdivisión dentro y entre Poblaciones de Chen rossi y Chen caerulescens caerulescens: Una Perspectiva MolecularResumen. Reanalizamos los datos de la región de control del ADN mitocondrial (ADNmt) de Quinn (1992), junto con nuevas secuencias de nueve individuos de la especie Chen caerulescens caerulescens y 10 de Chen rossi. Encontramos los mismos linajes divergentes que Quinn (1992) atribuyó a la separación vicariante de las poblaciones de C. c. caerulescens durante el Pleistoceno. Sin embargo, encontramos que las dos especies comparten dos linajes de haplotipos divergentes, y la distribución de “mismatch” en secuencias del ADNmt mostró multimodalidad con dos niveles de estructuración de la población. Estos patrones peculiares están de acuerdo con la hipótesis de que hubo dos episodios de hibridización en gansos del género Chen. Los datos históricos y de aloenzimas compilados por Cooke et al. (1988) también apoyan esta hipótesis (Avise et al. 1992). Además, la estructura de la población dentro de un grupo de haplotipos es consistente con la hipótesis de Cooke et al. (1988) acerca de la pasada alopatría entre los morfos azul y blanco de C. c. caerulescens.


Oikos ◽  
1993 ◽  
Vol 67 (2) ◽  
pp. 250 ◽  
Author(s):  
T. D. Williams ◽  
D. B. Lank ◽  
F. Cooke

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