Selection can facilitate diversification by inducing character displacement in mate choice traits that reduce the probability of maladaptive mating between lineages. Although reproductive character displacement (RCD) has been demonstrated in two-taxa case studies, the frequency of this process in nature is still debated. Moreover, studies have focused primarily on visual and acoustic traits, despite the fact that chemical communication is probably the most common means of species recognition. Here, we showed in a large, mostly sympatric, butterfly genus, a strong pattern of recurrent RCD for predicted male sex pheromone composition, but not for visual mate choice traits. Our results suggest that RCD is not anecdotal, and that selection for divergence in male sex pheromone composition contributed to reproductive isolation within the Bicyclus genus. We propose that selection may target olfactory mate choice traits as a more common sensory modality to ensure reproductive isolation among diverging lineages than previously envisaged.
Tradeoffs affect resource allocation during development and result in fitness consequences that drive the evolution of life history strategies. Yet despite their importance, we know little about the mechanisms underlying life history tradeoffs. Many species of Colias butterflies exhibit an alternative life history strategy (ALHS) where females divert resources from wing pigment synthesis to reproductive and somatic development. Due to this reallocation, a wing color polymorphism is associated with the ALHS: either yellow/orange or white. Here we map the locus associated with this ALHS in Colias crocea to a transposable element insertion located downstream of the Colias homolog of BarH-1, a homeobox transcription factor. Using CRISPR/Cas9 gene editing, antibody staining, and electron microscopy we find white-specific expression of BarH-1 suppresses the formation of pigment granules in wing scales and gives rise to white wing color. Lipid and transcriptome analyses reveal physiological differences associated with the ALHS. Together, these findings characterize a mechanism for a female-limited ALHS.
Tracking migratory movement of small animals with variable migration patterns is difficult with standard mark–recapture methods or genetic analysis. We used stable hydrogen isotope (δD) measurements of wings from European red admirals Vanessa atalanta to study several aspects of this species’ migration. In the central part of southern Europe we found large differences in δD values between red admirals sampled in autumn and spring supporting the hypothesis that reproduction takes place in the Mediterranean region during winter. There was also an apparent influx to southern Europe in the spring of individuals with a more southerly origin, since many samples had higher δD values and similar to those expected from coastal areas of North Africa. We found a clear seasonal difference in the δD values of red admirals sampled in northern Europe. Spring migrants arriving in northern Europe generally had high δD values that indicated a southerly origin. In autumn, δD values suggested that red admirals were mostly from regions close to the sampling sites, but throughout the sampling period there were always individuals with δD values suggesting non‐local origins. The migration pattern of this species is supposedly highly variable and plastic. δD differences between individuals in the western part of Europe were generally small making migratory patterns difficult to interpret. However, butterflies from western Europe were apparently isolated from those from north‐eastern Europe, since δD values in the western region rarely corresponded to those of autumn migrants from the north‐east. Use of δD data for inferring butterfly migration in Europe is complex, but our study showed that this technique can be used to help uncover previously unknown aspects of red admiral migration.
BackgroundButterflies of the subtribe Mycalesina have radiated successfully in almost all habitat types in Africa, Madagascar, the Indian subcontinent, Indo-China and Australasia. Studies aimed at understanding the reasons behind the evolutionary success of this spectacular Old World butterfly radiation have been hampered by the lack of a stable phylogeny for the group. Here, we have reconstructed a robust phylogenetic framework for the subtribe using 10 genes from 195 exemplar taxa.ResultsWe recovered seven well supported clades within the subtribe corresponding to the five traditional genera (Lohora, Heteropsis, Hallelesis, Bicyclus, Mycalesis), one as recently revised (Mydosama) and one newly revised genus (Culapa). The phylogenetic relationships of these mycalesine genera have been robustly established for the first time. Within the proposed phylogenetic framework, we estimated the crown age of the subtribe to be 40 Million years ago (Mya) and inferred its ultimate origin to be in Asia. Our results reveal both vicariance and dispersal as factors responsible for the current widespread distribution of the group in the Old World tropics. We inferred that the African continent has been colonized at least twice by Asian mycalesines within the last 26 and 23 Mya. In one possible scenario, an Asian ancestor gave rise to Heteropsis on continental Africa, which later dispersed into Madagascar and most likely back colonised Asia. The second colonization of Africa by Asian ancestors resulted in Hallelesis and Bicyclus on continental Africa, the descendants of which did not colonise other regions but rather diversified only in continental Africa. The genera Lohora and Mydosama are derivatives of ancestors from continental Asia.ConclusionOur proposed time-calibrated phylogeny now provides a solid framework within which we can implement mechanistic studies aimed at unravelling the ecological and evolutionary processes that culminated in the spectacular radiation of mycalesines in the Old World tropics.Electronic supplementary materialThe online version of this article (doi:10.1186/s12862-015-0449-3) contains supplementary material, which is available to authorized users.
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