Richard S. Peigler

Phylogenetic relationships of wild silkmoths (Lepidoptera: Saturniidae) inferred from four protein‐coding nuclear genes

Abstract The Saturniidae, or wild silkmoths, number approximately 1861 species in 162 genera and nine subfamilies including Cercophaninae and Oxyteninae. They include some of the largest and most spectacular of all Lepidoptera, such as the moon or luna moths, atlas moths, emperor moths, and many others. Saturniids have been important as sources of wild silk and/or human food in a number of cultures, and as models for comparative studies of genetics, development, physiology, and ecology. Seeking to improve the phylogenetic framework for such studies, we estimated relationships across Saturniidae, sampling all nine subfamilies plus all five tribes of Saturniinae. Seventy‐five exemplars (45 Saturniidae plus 30 bombycoid outgroups) were sequenced for four protein‐coding nuclear gene regions (5625 bp total), namely CAD (the fusion protein carbamoylphosphate synthetase/aspartate transcarbamylase/dihydroorotase), DDC (dopa decarboxylase), period, and wingless. The data, analyzed by parsimony and likelihood, gave a strongly resolved phylogeny at all levels. Relationships among subfamilies largely mirrored the pre‐cladistic hypothesis of Michener, albeit with significant exceptions, and there was definitive support for the morphology‐based proposal that Ludiinae form a tribe (Micragonini) within Saturniinae. In the latter subfamily, the African tribe Urotini was shown to be paraphyletic with respect to Bunaeini and Micragonini, also in accord with recent morphological findings. Relationships within the New World subfamilies Arsenurinae, Ceratocampinae and Hemileucinae nearly always accord with previous morphology‐based phylogenies when both are clearly resolved. Within Hemileucinae, Hemileucini are paraphyletic with respect to the monotypic Polythysanini. A preliminary biogeographical analysis supports ancestral restriction to the New World, followed by dispersal and/or vicariance splitting most of the family into a largely New World versus a largely Old World clade.

Multi-gene phylogeny of the Hemileuca maia complex (Saturniidae) across North America suggests complex phylogeography and rapid ecological diversification

The Hemileuca maia species complex occurs across the North American continent and consists of six named taxa, and several others that were recently synonymized. Taxa exhibit a wide span of adult flight periods, dramatic shifts in host‐plant use and occur in a range of habitats, all of which would suggest unrecognized diversity. We used one mitochondrial and three nuclear genes to generate 3900 bp per individual, including samples from every ecotype in the species group across the United States from New England to central Florida to California. We assessed phylogenetic relationships using both maximum likelihood and Bayesian phylogenetic methods. Results suggest very low levels of divergence across most of the continent and low levels of genetic structure – even between some recognized species that maintain clear ecological difference in sympatry. Our results suggest that meaningful and localized ecological divergence may occur in the absence of easily recognizable genetic divergence, due to either ongoing gene flow or the recent diversification in the group.

Phylogenomics supports incongruence between ecological specialization and taxonomy in a charismatic clade of buck moths

Local adaptation can be a fundamental component of speciation, but its dynamics in relation to gene flow are not necessarily straightforward. Herbivorous taxa with localized host plant or habitat specialization across their geographic range are ideal models for investigating the patterns and constraints of local adaptation and its impact on diversification. The charismatic, day‐flying moths of the Hemileuca maia species complex (Lepidoptera: Saturniidae) are such taxa, as they are geographically widespread, exhibit considerable ecological and morphological variability and host and habitat specificity, but apparently lack genetic differentiation across their range. Here, we use genomewide single nucleotide polymorphisms to assess relationships and population structure of this group across North America and investigate the scales where genomic divergence correlates with adaptive ecological characteristics. In contrast to previous genetic studies of the group, we find broad‐ and fine‐scale genetic differentiation between lineages, which is at odds with various levels of taxonomic description and recognition of conservation units. Furthermore, ecological specialization only explains some fine‐scale genetic differentiation, and across much of the groups range, local adaptation is apparently occurring in the face of strong gene flow. These results provide unprecedented insight into drivers of speciation in this group, the relationship between taxonomy and genomics‐informed species boundaries and conservation management of internationally protected entities. Broadly, this system provides a model for understanding how local adaptation in an herbivore can arise and be maintained in the face of apparently strong gene flow, and the importance of geographic isolation in generating genomic divergence, despite a lack of ecological divergence.