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First published online March 27, 2009
Journal of Experimental Biology 212, 1087-1091 (2009)
Published by The Company of Biologists 2009
doi: 10.1242/jeb.024257
Sex-specific developmental plasticity in response to yolk corticosterone in an oviparous lizard
1 Edward Grey Institute, Department of Zoology, University of Oxford, Oxford OX1
3PS, UK
2 School of Biological Sciences, University of Wollongong, Wollongong, NSW 2522,
Australia
3 Department of Animal and Plant Sciences, University of Sheffield, Sheffield
N10 2TN, UK
4 School of Health Sciences, University of Wollongong, Wollongong, NSW 2522,
Australia
Author for correspondence (e-mail: tobias.uller{at}zoo.ox.ac.uk)
Accepted 22 January 2009
Corticosterone exposure during prenatal development as a result of maternal upregulation of circulating hormone levels has been shown to have effects on offspring development in mammals. Corticosterone has also been documented in egg yolk in oviparous vertebrates, but the extent to which this influences phenotypic development is less studied. We show that maternal corticosterone is transferred to egg yolk in an oviparous lizard (the mallee dragon, Ctenophorus fordi Storr), with significant variation among clutches in hormone levels. Experimental elevation of yolk corticosterone did not affect hatching success, incubation period or offspring sex ratio. However, corticosterone did have a sex-specific effect on skeletal growth during embryonic development. Male embryos exposed to relatively high levels of corticosterone were smaller on average than control males at hatching whereas females from hormone-treated eggs were larger on average than control females. The data thus suggest that males are not just more sensitive to the detrimental effects of corticosterone but rather that the sexes may have opposite responses to corticosterone during development. Positive selection on body size at hatching for both sexes in this species further suggests that increased corticosterone in egg yolk may have sex-specific fitness consequences, with potential implications for sex allocation and the evolution of hormone-mediated maternal effects.
Key words: Ctenophorus fordi, hormones, phenotypic plasticity
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