Is Intraclutch Egg-Size Variation Adaptive in the Lesser Snow Goose?

Oikos ◽  
1993 ◽  
Vol 67 (2) ◽  
pp. 250 ◽  
Author(s):  
T. D. Williams ◽  
D. B. Lank ◽  
F. Cooke
Oecologia ◽  
1993 ◽  
Vol 96 (3) ◽  
pp. 331-338 ◽  
Author(s):  
T. D. Williams ◽  
D. B. Lank ◽  
F. Cooke ◽  
R. F. Rockwell

1994 ◽  
Vol 25 (2) ◽  
pp. 149 ◽  
Author(s):  
Gregory J. Robertson ◽  
Evan G. Cooch ◽  
David B. Lank ◽  
Robert F. Rockwell ◽  
F. Cooke

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

The Auk ◽  
2005 ◽  
Vol 122 (2) ◽  
pp. 509-522 ◽  
Author(s):  
Rita Hargitai ◽  
János Török ◽  
László Tóth ◽  
Gergely Hegyi ◽  
Balázs Rosivall ◽  
...  

AbstractEgg size is a particularly important life-history trait mediating maternal influences on offspring phenotype. Females can vary their egg-size investment in relation to environmental circumstances, their own breeding condition, and the quality of their mate. Here we analyzed inter- and intraclutch variation in egg size in the Collared Flycatcher (Ficedula albicollis) on the basis of eight years of data. According to our results, mean egg size increased with female condition, but did not differ among young, middle-aged, and old females. The male’s age, body size, and forehead patch size did not influence egg size; thus, we found no evidence for differential investment in egg size in relation to male quality. We found no effect of laying date on egg size when controlling for ambient temperature during the egg formation period, yet temperature had a significant effect on egg size. That result indicates proximate constraints on egg formation. Furthermore, we report on annual differences in intraclutch egg-size variation. Egg size increased within clutches in years with a warm prelaying period; whereas in years when the weather during that period was cold, there was no significant intraclutch trend. Proximate considerations seem to explain the observed patterns of intraclutch egg-size variation; however, we cannot reject the adaptive explanation. Mean egg size and intraclutch egg-size variation were unrelated to clutch size. Therefore, we found no evidence for a trade-off between size and number of eggs within a clutch.


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.


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