Behavioral Ecology Advance Access first published online on June 6, 2006
This version published online on August 4, 2006
Behavioral Ecology, doi:10.1093/beheco/arl007
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Departamento de Ecología Evolutiva, Museo Nacional de Ciencias Naturales, Consejo Superior de Investigaciones Científicas, José Gutiérrez Abascal 2, 28006 Madrid, Spain
* To whom correspondence should be addressed. The differential environmental sensitivity of the sexes has strong implications in the evolutionary history of species as it can alter sexual size dimorphism, population sex ratios, and the faculty of parents to manipulate offspring sex in relation to environmental conditions. We studied sexual differences in hatching patterns and evaluated sex- and size-related mortality in relation to hatching order and brood sex ratios in the chinstrap penguin Pygoscelis antarctica, a moderately size-dimorphic species, with a modal clutch size of 2 eggs. We found that male, second-hatched, and large eggs showed shorter hatching periods than female, first-hatched, and small eggs. We also found a male-biased mortality of nestlings in the colony. However, male mortality patterns differed depending on the brood sex ratio composition. Mortality of male chicks in all-male broods was higher than in mixed broods and higher than female mortality in all-female broods. Contrary, females from mixed brood showed higher mortality than their male nest mates and higher too than females in all-female broods. Second-hatched chicks also suffered from higher mortality than first-hatched chicks. Our results indicate that both the superior competitive capacity and the higher energy demand of the larger sex constitute 2 causal factors explaining patterns of sex-biased mortality. Both factors occur in the same species and in different situations of sibling competition shaped by brood sex ratio composition. This study constitutes a good example of how patterns of sex-related mortality can vary depending on nest environmental circumstances. Furthermore, our study suggests that hatching period can be a mechanism underlying sexual differences in the embryonic period of birds. The manuscript type has been corrected to "Research Article."
Received October 14, 2005
Revised March 28, 2006
Accepted May 5, 2006
Article
Hatching order and size-dependent mortality in relation to brood sex ratio composition in chinstrap penguins
Juan A. Fargallo 1 *, Vicente Polo 1, Liesbeth de Neve 1, José Martín 1, José A. Dávila 2, and Manuel Soler 3
2 Instituto de Investigación en Recursos Cinegéticos, Consejo Superior de Investigaciones Científicas-Universidad de Castilla, La Mancha, Ronda de Toledo s/n, E-13005 Ciudad Real, Spain
3 Departamento de Biología Animal y Ecología, Facultad de Ciencias, Universidad de Granada, E-18071 Granada, Spain
Juan A. Fargallo, E-mail: fargallo{at}mncn.csic.es
Abstract
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  D. Parejo and N. Silva Methionine supplementation influences melanin-based plumage colouration in Eurasian kestrel, Falco tinnunculus, nestlings J. Exp. Biol., November 1, 2009; 212(21): 3576 - 3582. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 P. Vergara and J. A. Fargallo Sex, melanic coloration, and sibling competition during the postfledging dependence period Behav. Ecol., July 1, 2008; 19(4): 847 - 853. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
L. De Neve, J. A. Fargallo, P. Vergara, J. A. Lemus, M. Jaren-Galan, and I. Luaces Effects of maternal carotenoid availability in relation to sex, parasite infection and health status of nestling kestrels (Falco tinnunculus) J. Exp. Biol., May 1, 2008; 211(9): 1414 - 1425. [Abstract] [Full Text] [PDF]
|
|