Hatching order and size-dependent mortality in relation to brood sex ratio composition in chinstrap penguins

被引:25
作者
Fargallo, Juan A.
Polo, Vicente
de Neve, Liesbeth
Martin, Jose
Davila, Jose A.
Soler, Manuel
机构
[1] CSIC, Dept Ecol Evolutiva, Museo Nacl Ciencias Nat, Madrid 28006, Spain
[2] Univ Castilla La Mancha, Inst Invest Recursos Cineget, Consejo Super Invest Cientif, E-13005 Ciudad Real, Spain
[3] Univ Granada, Fac Ciencias, Dept Biol Anim & Ecol, E-18071 Granada, Spain
关键词
egg size; hatching asynchrony; hatching period; nestling survival; Pygoscelis antarctica;
D O I
10.1093/beheco/arl007
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
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.
引用
收藏
页码:772 / 778
页数:7
相关论文
共 63 条
[21]   Does sex-biased hatching order in bald eagles vary with food resources? [J].
Dzus, EH ;
Bortolotti, GR ;
Gerrard, JM .
ECOSCIENCE, 1996, 3 (03) :252-258
[22]   EMBRYONIC FINE TUNING OF PIPPED EGG TEMPERATURE IN THE AMERICAN WHITE PELICAN [J].
EVANS, RM .
ANIMAL BEHAVIOUR, 1990, 40 :963-968
[23]  
Fargallo JA, 2003, EVOL ECOL RES, V5, P549
[24]   Inter-sexual differences in the immune response of Eurasian kestrel nestlings under food shortage [J].
Fargallo, JA ;
Laaksonen, T ;
Pöyri, V ;
Korpimäki, E .
ECOLOGY LETTERS, 2002, 5 (01) :95-101
[25]   Nest size and hatchling sex ratio in chinstrap penguins [J].
Fargallo, JA ;
Daávila, JA ;
Potti, J ;
de León, A ;
Polo, V .
POLAR BIOLOGY, 2004, 27 (06) :339-343
[26]   Multiple incentives for parental optimism and brood reduction in blackbirds [J].
Forbes, S ;
Grosshans, R ;
Glassey, B .
ECOLOGY, 2002, 83 (09) :2529-2541
[27]  
Gil D, 2003, ARDEOLA, V50, P281
[28]   Why are birds' eggs speckled? [J].
Gosler, AG ;
Higham, JP ;
Reynolds, SJ .
ECOLOGY LETTERS, 2005, 8 (10) :1105-1113
[29]   RELATIONSHIPS BETWEEN EGG SIZE, CHICK SIZE AT HATCHING, AND CHICK SURVIVAL IN THE WHIMBREL NUMENIUS-PHAEOPUS [J].
GRANT, MC .
IBIS, 1991, 133 (02) :127-133
[30]   SEX OF THE LAST WILD SPIXS MACAW [J].
GRIFFITHS, R ;
TIWARI, B .
NATURE, 1995, 375 (6531) :454-454