Climate affects geographic variation in host-plant but not mating preferences of Timema cristinae stick-insect populations (original) (raw)
Related papers
Evolution, 2005
The evolution of ecological specialization has been a central topic in ecology because specialized adaptations to divergent environments can result in reproductive isolation and facilitate speciation. However, the order in which different aspects of habitat adaptation and habitat preference evolve is unclear. Timema walking-stick insects feed and mate on the host plants on which they rest. Previous studies of T. cristinae ecotypes have documented divergent, host-specific selection from visual predators and the evolution of divergent host and mate preferences between populations using different host-plant species (Ceanothus or Adenostoma). Here we present new data that show that T. podura, a nonsister species of T. cristinae, has also formed ecotypes on these host genera and that in both species these ecotypes exhibit adaptive divergence in color-pattern and host preference. Color-pattern morphs exhibit survival trade-offs on different hosts due to differential predation. In contrast, fecundity trade-offs on different hosts do not occur in either species. Thus, host preference in both species has evolved before divergent physiological adaptation but in concert with morphological adaptations. Our results shed light onto which traits are involved in the initial stages of ecological specialization and ecologically based reproductive isolation.
Journal of Insect Behavior, 2014
In primitively eusocial insects, air temperature is the environmental factor that primarily affects colony cycle. Several studies demonstrated interspecific differences in the adaptation of eusocial insects to local air temperature. Nevertheless, studies on intraspecific adaptations are rare. In this study, we investigate the influence of air temperature on local adaptations in behavior and colony productivity of Polistes biglumis foundresses living in warm and cold temperate zones. We hypothesized that foundresses from warm temperate zones would show a higher activity level compared to those from cold temperate zones before brood emergence, based on differences in air temperature between the two zones. After brood emergence, we expected a reduced foundress activity level in the warm climate zone, due to workers' help. In contrast, foundresses living in the cold-climate zone, which do not produce workers, were expected to remain active throughout the nesting season. We also hypothesized that colony productivity was higher in warm-climate colonies. As expected, warm-climate foundresses reduced their activity level after brood emergence and, with their relatively large number of workers, continued egg production throughout the nesting season. Further studies are necessary to assess if these intraspecific differences are attributable to phenotypic plasticity or genetic divergence.
Natural selection and divergence in mate preference during speciation
Genetica, 2007
Sexual isolation can evolve due to natural selection against hybrids (reinforcement). However, many different forms of hybrid dysfunction, and selective processes that do not involve hybrids, can contribute to the evolution of sexual isolation. Here we review how different selective processes affect the evolution of sexual isolation, describe approaches for distinguishing among them, and assess how they contribute to variation in sexual isolation among populations of Timema cristinae stick-insects. Pairs of allopatric populations of T. cristinae living on different host-plant species exhibit greater sexual isolation than those on the same host, indicating that some sexual isolation has evolved due to host adaptation. Sexual isolation is strongest in regions where populations on different hosts are in geographic contact, a pattern of reproductive character displacement that is indicative of reinforcement. Ecological costs to hybridization do occur but traits under ecological selection (predation) do not co-vary strongly with the probability of between-population mating such that selection on ecological traits is not predicted to produce a strong correlated evolutionary response in mate preference. Moreover, F1 hybrid egg inviability is lacking and the factors contributing to reproductive character displacement require further study. Finally, we show that sexual isolation involves, at least in part, olfactory communication. Our results illustrate how understanding of the evolution of sexual isolation can be enhanced by isolating the roles of diverse ecological and evolutionary processes.
Sexual dimorphism dominates divergent host plant use in stick insect trophic morphology
BMC Evolutionary Biology, 2013
Clear examples of ecological speciation exist, often involving divergence in trophic morphology. However, substantial variation also exists in how far the ecological speciation process proceeds, potentially linked to the number of ecological axes, traits, or genes subject to divergent selection. In addition, recent studies highlight how differentiation might occur between the sexes, rather than between populations. We examine variation in trophic morphology in two host-plant ecotypes of walking-stick insects (Timema cristinae), known to have diverged in morphological traits related to crypsis and predator avoidance, and to have reached an intermediate point in the ecological speciation process. Here we test how host plant use, sex, and rearing environment affect variation in trophic morphology in this species using traditional multivariate, novel kernel density based and Bayesian morphometric analyses. Results: Contrary to expectations, we find limited host-associated divergence in mandible shape. Instead, the main predictor of shape variation is sex, with secondary roles of population of origin and rearing environment. Conclusion: Our results show that trophic morphology does not strongly contribute to host-adapted ecotype divergence in T. cristinae and that traits can respond to complex selection regimes by diverging along different intraspecific lines, thereby impeding progress toward speciation.
Reproductive isolation driven by the combined effects of ecological adaptation and reinforcement
Proceedings of the Royal Society B: Biological Sciences, 2003
Recent years have seen a resurgence of interest in the process of speciation but few studies have elucidated the mechanisms either driving or constraining the evolution of reproductive isolation. In theory, the direct effects of reinforcing selection for increased mating discrimination where interbreeding produces hybrid offspring with low fitness and the indirect effects of adaptation to different environments can both promote speciation. Conversely, high levels of homogenizing gene flow can counteract the forces of selection. We demonstrate the opposing effects of reinforcing selection and gene flow in Timema cristinae walking-stick insects. The magnitude of female mating discrimination against males from other populations is greatest when migration rates between populations adapted to alternate host plants are high enough to allow the evolution of reinforcement, but low enough to prevent gene flow from eroding adaptive divergence in mate choice. Moreover, reproductive isolation is strongest under the combined effects of reinforcement and adaptation to alternate host plants. Our findings demonstrate the joint effects of reinforcement, ecological adaptation and gene flow on progress towards speciation in the wild.
2005
It has long been supposed that variation in mating phenology leads to assortative mating, but its inherent frequency dependence has not been examined. When plants in a population vary in their flowering schedule, the phenotypic (and genetic) composition of the mating pool changes over the season; this causes phenological assortative mating even if pollen is exchanged at random during each interval of the season. Phenotype frequencies govern this temporal shift in the mating pool and this makes phenological assortative mating frequency dependent. We studied phenological assortative mating in four steps. First, we derived a method to estimate the phenotypic correlation between mates from flowering schedules; this correlation, symbolized by ρ, is the standard measure of assortative mating. Next, in a one-locus, two-allele system, we showed that the correlation between mates decreases as one or the other allele approaches fixation, but increases as the population deviates from Hardy-Weinberg proportions. Third, we showed that unlike assortative mating based on fixed preferences, the level of phenological assortment in one generation influences the level of assortment in the next, such that ρ reaches an equilibrium value that depends on allele frequencies. Finally, we contrasted the effects of frequency-dependent, phenological assortative mating on directional selection to the effects of fixed levels of assortative mating. When allelic effects were additive, frequency dependence slightly accelerated the selection response, compared with a fixed ρ. When one allele was dominant, phenological assortment slightly decelerated the selection response. Similarities between assortative mating through phenology and through habitat preference can cause the latter also to be frequency dependent.