Allocation trade-offs are predicted to affect evolutionary dynamics, including the evolution of sexual dimorphism. In gynodioecious species, where populations have both females and hermaphrodites, selection may result in sexual dimorphism in individual traits or trait correlations because, in contrast to females, hermaphrodites acquire fitness through both male and female function. Using the gynodioecious species Silerie vul^aris, we measured reproductive traits (ovule number, ovule size, anther size, and floral traits related to display) and a vegetative trait (intemode length) among plants growing under full sun and foliar shade treatments. We tested for sex-specific correlation structures as ' I well as trait plasticity and the sensitivity of correlation structures to the light environment. Hermaphrodites exhibited ' I a fixed trade-off between anther size and ovule size, whereas females exhibited an ovule siz^number trade-off, l-or a I few traits, we detected plasticity to light treatment and plasticity that differed significantly between sexes across light j, treatments. Fxposure ro foliar shade resulted in a sex-specific trade-off between vegetative and reproductive allegation; hermaphrodites exhibited a negative correlation (trade-off) between intemode elongation and ovule number, whereas females showed a marginally significant, positive correlation between these two traits. The tradeoffs observed in hermaphrodites are of particular evolutionary relevance, suggesting that hermaphrodites will evolve to Income increasingly male and populations increasingly sexually dimorphic.