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Olfaction is an important sense that has contributed to reproductive isolation and speciation in many taxa. However, in birds, olfaction and its potential role in communication has historically been neglected. Thus, what role olfaction plays in avian speciation is mostly unknown. Here, we aim to guide future research by highlighting the likely potential for olfaction to contribute to reproductive isolation and speciation in birds. First, we detail the best-understood example found thus far that is consistent with reproductive isolation by olfaction in birds: black-capped and Carolina chickadees. These species show interspecific differences in preen oil chemistry and conspecific odour preferences within their natural hybrid zone. We then suggest a number of promising avenues for future research and the kinds of systems, approaches and evidence that would help to advance this severely understudied area. In sum, the growing body of research into the chemical ecology of birds suggests an important role of olfaction in many areas of avian life. Future research will be necessary to determine to what extent olfaction contributes to the formation and maintenance of species boundaries in birds. 

Abstract Determining the genetic architecture of traits involved in adaptation and speciation is one of the key components of understanding the evolutionary mechanisms behind biological diversification. Hybrid zones provide a unique opportunity to use genetic admixture to identify traits and loci contributing to partial reproductive barriers between taxa. Many studies have focused on the temporal dynamics of hybrid zones, but geographical variation in hybrid zones that span distinct ecological contexts has received less attention. We address this knowledge gap by analyzing hybridization and introgression between black-capped and Carolina chickadees in two geographically remote transects across their extensive hybrid zone, one located in eastern and one in central North America. Previous studies demonstrated that this hybrid zone is moving northward as a result of climate change but is staying consistently narrow due to selection against hybrids. In addition, the hybrid zone is moving ~5× slower in central North America compared to more eastern regions, reflecting continent-wide variation in the rate of climate change. We use whole genome sequencing of 259 individuals to assess whether variation in the rate of hybrid zone movement is reflected in patterns of hybridization and introgression, and which genes and genomic regions show consistently restricted introgression in distinct ecological contexts. Our results highlight substantial similarities between geographically remote transects and reveal large Z-linked chromosomal rearrangements that generate measurable differences in the degree of gene flow between transects. We further use simulations and analyses of climatic data to examine potential factors contributing to continental-scale nuances in selection pressures. We discuss our findings in the context of speciation mechanisms and the importance of sex chromosome inversions in chickadees and other species.