scholarly journals Sex differences in the effects of juvenile and adult diet on age-dependent reproductive effort

2015 ◽  
Vol 28 (5) ◽  
pp. 1067-1079 ◽  
Author(s):  
T. M. Houslay ◽  
J. Hunt ◽  
M. C. Tinsley ◽  
L. F. Bussière
Hypertension ◽  
2019 ◽  
Vol 74 (Suppl_1) ◽  
Author(s):  
Franco J Puleo ◽  
Alissa A Frame ◽  
Parul Chaudhary ◽  
Richard D Wainford

2015 ◽  
Vol 282 (1805) ◽  
pp. 20150050 ◽  
Author(s):  
Diogo S. M. Samia ◽  
Anders Pape Møller ◽  
Daniel T. Blumstein ◽  
Theodore Stankowich ◽  
William E. Cooper

Sexual selection is a powerful evolutionary mechanism that has shaped the physiology, behaviour and morphology of the sexes to the extent that it can reduce viability while promoting traits that enhance reproductive success. Predation is one of the underlying mechanisms accounting for viability costs of sexual displays. Therefore, we should expect that individuals of the two sexes adjust their anti-predator behaviour in response to changes in predation risk. We conducted a meta-analysis of 28 studies (42 species) of sex differences in risk-taking behaviour in lizards and tested whether these differences could be explained by sexual dichromatism, by sexual size dimorphism or by latitude. Latitude was the best predictor of the interspecific heterogeneity in sex-specific behaviour. Males did not change their escape behaviour with latitude, whereas females had increasingly reduced wariness at higher latitudes. We hypothesize that this sex difference in risk-taking behaviour is linked to sex-specific environmental constraints that more strongly affect the reproductive effort of females than males. This novel latitudinal effect on sex-specific anti-predator behaviour has important implications for responses to climate change and for the relative roles of natural and sexual selection in different species.


2011 ◽  
Vol 21 (3) ◽  
pp. 244-252 ◽  
Author(s):  
Liljana Mervic ◽  
Ulrike Leiter ◽  
Friedegund Meier ◽  
Thomas Eigentler ◽  
Andrea Forschner ◽  
...  

2009 ◽  
Vol 23 (3) ◽  
pp. 602-611 ◽  
Author(s):  
Felix Zajitschek ◽  
John Hunt ◽  
Michael D. Jennions ◽  
Matthew D. Hall ◽  
Robert C. Brooks

2016 ◽  
Vol 94 (5) ◽  
pp. 311-321 ◽  
Author(s):  
A. Morin ◽  
M. Rughetti ◽  
S. Rioux-Paquette ◽  
M. Festa-Bianchet

In long-lived mammals, costs of reproduction may vary with age. The terminal investment hypothesis predicts greater reproductive effort as females approach the end of their life expectancy. We monitored 97 individually marked female Alpine chamois (Rupicapra rupicapra (L., 1758)) between 2007 and 2013 to determine how age-specific reproduction affected body mass and subsequent reproductive success. We captured and weighed females between April and August and monitored reproductive success from April to October through mother–kid associations. Reproductive success was strongly age-dependent and peaked at 70% for prime-aged females (4–7 years). Reproductive senescence began at 8 years, earlier than reported by other studies of ungulates. There was no clear evidence of reproductive costs in any age class. Reproductive success was very heterogeneous for old females, suggesting variability in the onset of senescence. Old females were less likely to reproduce in poor years despite being heavier than prime-aged females, suggesting reproductive restraint in late life rather than terminal investment. Female mass remained stable from May to August with no effect of lactation. Our results suggest that chamois reproductive strategy becomes increasingly conservative with age, resulting in no detectable costs of reproduction.


2016 ◽  
Vol 46 ◽  
pp. 11-17 ◽  
Author(s):  
Yoshiyuki Kobayashi ◽  
Hiroaki Hobara ◽  
Thijs A. Heldoorn ◽  
Makiko Kouchi ◽  
Masaaki Mochimaru

2002 ◽  
Vol 14 (6) ◽  
pp. 693-698 ◽  
Author(s):  
Zygmunt Welon ◽  
Alicja Szklarska ◽  
Tadeusz Bielicki ◽  
Robert M. Malina

2013 ◽  
Vol 9 (2) ◽  
pp. 20121078 ◽  
Author(s):  
Catherine L. Hayes ◽  
Isobel Booksmythe ◽  
Michael D. Jennions ◽  
Patricia R. Y. Backwell

Theory suggests that reproductive effort generally increases with age, but life-history models indicate that other outcomes are possible. Empirical data are needed to quantify variation in actual age-dependence. Data are readily attainable for females (e.g. clutch per egg size), but not for males (e.g. courtship effort). To quantify male effort one must: (i) experimentally control for potential age-dependent changes in female presence; and, crucially, (ii) distinguish between the likelihood of courtship being initiated, the display rate, and the total time invested in courting before stopping (‘courtship persistence’). We provide a simple experimental protocol, suitable for many taxa, to illustrate how to obtain this information. We studied courtship waving by male fiddler crabs, Uca annulipes . Given indeterminate growth, body size is correlated with age. Larger males were more likely to wave at females and waved more persistently. They did not, however, have a higher courtship rate (waves per second). A known female preference for males with higher display rates explains why, once waving is initiated, all males display at the same rate.


Sign in / Sign up

Export Citation Format

Share Document