Neural divergence and hybrid disruption between ecologically isolated Heliconius butterflies

Abstract

The importance of behavioural evolution during speciation is well established, but we know little about how this is manifest in sensory and neural systems. Although a handful of studies have linked specific neural changes to divergence in host or mate preferences associated with speciation, how brains respond to broad environmental transitions, and whether this contributes to reproductive isolation, remains unknown. Here, we examine divergence in brain morphology and neural gene expression between closely related, but ecologically distinct, Heliconius butterflies. Despite on-going gene flow, sympatric species pairs within the melpomene-cydno complex are consistently separated across a gradient of open to closed forest and decreasing light intensity. By generating quantitative neuroanatomical data for 107 butterflies, we show that H. melpomene and H. cydno have substantial shifts in brain morphology across their geographic range, with divergent structures clustered in the visual system. These neuroanatomical differences are mirrored by extensive divergence in neural gene expression. Differences in both morphology and gene expression are heritable, exceed expected rates of neutral divergence, and result in intermediate traits in first generation hybrid offspring. This likely disrupts neural system function, leading to a mismatch between the environment and the behavioral response of hybrids. Our results suggest that disruptive selection on both neural function and external morphology result in coincident barriers to gene flow, thereby facilitating speciation.