Abstract

BackgroundClear 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.ResultsContrary 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.ConclusionOur 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.

Highlights

  • Clear examples of ecological speciation exist, often involving divergence in trophic morphology

  • 97% of males were assigned to one cluster with greater than 95% posterior probability, while 96% of females were assigned to a different cluster with greater than 95% posterior probability (Figure 2A)

  • Ninety-one percent of females were assigned to the same cluster with greater than 95% posterior probability

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Summary

Introduction

Clear examples of ecological speciation exist, often involving divergence in trophic morphology. Observed variation in the progress towards ecological speciation may be due to differential divergence time, degree of gene flow, strength of divergent selection, and the inherent genetic architectures underlying adaptive phenotypes [5,6,7,8]. Another factor may be the number of ecological dimensions, traits or genes upon which divergent selection acts [3,4,5,6,8,9]. Divergence can occurs to varying degrees among various traits, with some contributing more toward population divergence and speciation than others [4,5,8,11,12]

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