Abstract
AbstractAn optimal timing for diapause induction through the sexual production of dormant propagules is expected in organisms with temporary populations. Yet, empirical studies often find high within‐population genetic variation in the sexual production of such propagules, suggesting that this is a common feature of such organisms.Here, we hypothesize that genetic variation in the propensity to produce dormant propagules,Pd, is maintained by a genotype‐by‐environment interaction in clonal reproductive rates, where fast‐growing genotypes within an environment should delay diapause relative to slow‐growing genotypes. From this, we derive two predictions. First, if reaction norms of clonal reproduction cross between two environments, the genetic correlation ofPdbetween these environments should be negative. Second, the correlation between plasticity values of clonal reproduction andPdshould be negative.We tested these predictions by quantifying ephippia production in genotypes of a population of the facultative sexual cladoceranDaphnia magnaat two temperatures. The population biomass at the onset of ephippia production was used as a measure ofPd, whereas juvenile somatic growth rate was used as a proxy for clonal reproductive rate. Plasticity for both measurements was derived from thermal reaction norms.Our results did not support either prediction, as neither the genetic correlation ofPdbetween environments, nor the correlation between plasticity values of growth andPdwere found to be significant.Our results suggest that genetic variation in the timing of diapause is not maintained by genetic differences in thermal clonal reproduction reaction norms. We propose as an alternative hypothesis that if there is variation across years in how the environment deteriorates over a season, fluctuating selection may favor genotypes with differentPdbetween years.
Highlights
The timing of reproduction is a crucial life history trait (Stearns, 2000)
We hypothesize that genetic variation in the propensity to produce dormant propagules, Pd, is maintained by a genotype-by-environment interaction in clonal reproductive rates, where fast-growing genotypes within an environment should delay diapause relative to slow-g rowing genotypes
We tested these predictions by quantifying ephippia production in genotypes of a population of the facultative sexual cladoceran Daphnia magna at two temperatures
Summary
The timing of reproduction is a crucial life history trait (Stearns, 2000). This is true for many organisms living in temperate environments, where conditions for successful growth and reproduction are limited to certain time horizons (Gotthard, 2001). If this G × E interaction is strong, it can generate an “ecological crossover” where different genotypes are superior in different environments (Ellner & Hairston, 1994; Gillespie & Turelli, 1989; Higginson & Reader, 2009; Turelli & Barton, 2004) This should lead to corresponding differences in Pd across environments, and different optimal timing of making the switch from asexual to sexual reproduction in an environment that declines in quality towards the end of the season (Figure 1). Prati and Schmid (2000) showed a genetic tradeoff between flowering and rooting (i.e. between sexual reproduction and clonal growth), where flowering showed a G × E interaction that corresponded with a G × E interaction in rooting Such a trade-off might apply in the case of clonal versus sexual reproduction in facultative parthenogenetic animals, because the same female reproductive organs are used for both types of reproduction. Thermal reaction norms of somatic growth rate represent a good proxy for reaction norms of clonal reproduction
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