Phenotypic plasticity is predicted to facilitate individual survival and/or evolve in response to novel environments. Plasticity that facilitates survival should both permit colonization and act as a buffer against further evolution, with contemporary and derived forms predicted to be similarly plastic for a suite of traits. On the other hand, given the importance of plasticity in maintaining internal homeostasis, derived populations that encounter greater environmental heterogeneity should evolve greater plasticity. We tested the evolutionary significance of phenotypic plasticity in coastal British Columbian postglacial populations of threespine stickleback (Gasterosteus aculeatus) that evolved under greater seasonal extremes in temperature after invading freshwater lakes from the sea. Two ancestral (contemporary marine) and two derived (contemporary freshwater) populations of stickleback were raised near their thermal tolerance extremes, 7 and 22 °C. Gene expression plasticity was estimated for more than 14,000 genes. Over five thousand genes were similarly plastic in marine and freshwater stickleback, but freshwater populations exhibited significantly more genes with plastic expression than marine populations. Furthermore, several of the loci shown to exhibit gene expression plasticity have been previously implicated in the adaptive evolution of freshwater populations, including a gene involved in mitochondrial regulation (PPARAa). Collectively, these data provide molecular evidence that highlights the importance of plasticity in colonization and adaptation to new environments.

Abstract. The trade-off between current and future reproduction has led many organisms experiencing stochastic reproductive opportunities to be flexible in their resource acquisition and allocation rules. Many parasitoid wasps display flexibility in choosing to host-feed or oviposit on a host and possess an ovarian system enabling nutrient reallocation through egg resorption.The aim of this work is to assess the complementary adaptive values of host-feeding and egg resorption as functions of host density in a synovigenic (maturing eggs throughout its adult life) parasitoid, Eupelmus vuilleti (Hymenoptera: Eupelmidae), for which there is a uniquely large base of relevant knowledge. We developed a series of models of increasing complexity, starting from a simple analytical model without egg resorption and moving on to data-rich stochastic dynamic programming models (SDP), without and with resorption.The analytical model enabled the characterization of two, long-and short-term, foraging strategies which determine host usage. Oviposition is favored at low host densities (leading to the short-term strategy), while host-feeding is favored at high host densities (leading to the long-term strategy). The change of strategy occurs abruptly at intermediate host densities. The SPD models not only confirmed these predictions, but also identified smaller regions of decisions driven by day/night cycles and approaching death and predicted major shifts in daily activity patterns according to the chosen strategy. The fitness gain due to resorption is highest at intermediate host densities, where females adopt the riskier but more profitable long-term strategy. Such a result contrasts with the generally held view, which assumes highest gains at the lowest host densities. A counterintuitive result is the higher prevalence of host-feeding associated with the ability to resorb eggs.Considering egg resorption as a last-resort strategy is underestimating its adaptive value, which is best understood with reference to other sources of nutrients. Its deterministic and controllable nature acts as insurance to forage and oviposit at low host densities, despite irregular food availability and potential death through starvation. Thus timing, not so much overall energy gain, matters in egg resorption. The approach can be extended to other situations, and we highlight an unexpected analogy of our results with the hoarding behavior of vertebrates.

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