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Mikkelsen, E. K.

Publications and source records attributed to Mikkelsen, E. K..

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Ongoing production of low-fitness hybrids limits range overlap between divergent cryptic species

Contact zones between recently-diverged taxa provide opportunities to examine the causes of reproductive isolation and to examine the processes that determine whether two species can coexist over a broad region. The Pacific Wren (Troglodytes pacificus) and the Winter Wren (Troglodytes hiemalis) are two morphologically similar songbird species that started diverging about 4 million years ago, older than most sister species pairs. The ranges of these species come into narrow contact in western Canada, where the two species remain distinct in sympatry. To assess evidence for differentiation, hybridization, and introgression in this system, we examined variation in over 250,000 single nucleotide polymorphism markers distributed across the genomes of the two species. The two species formed highly divergent genetic clusters, consistent with long-term differentiation. In a set of 75 individuals from allopatry and sympatry, two first-generation hybrids (i.e., F1s) were detected, indicating only moderate levels of assortative mating between these taxa. We found no recent backcrosses or F2s or other evidence of recent breeding success of F1 hybrids, indicating very low or zero fitness of F1 hybrids. Examination of genomic variation shows evidence for only a single backcrossing event in the distant past. The sizeable rate of hybridization combined with very low fitness of F1 hybrids is expected to result in a population sink in the contact zone, largely explaining the narrow overlap of the two species. If such dynamics are common in nature, they could explain the narrow range overlap often observed between pairs of closely related species. Additionally, we present evidence for a rare duplication of a large chromosomal segment from an autosome to the W chromosome, the female-specific sex chromosome in birds.

evolutionary biology

Signatures of mito-nuclear climate adaptation in a warbler species complex

Mitochondrial (mtDNA) and nuclear (nDNA) genes interact to govern metabolic pathways of mitochondria. When differentiated populations interbreed at secondary contact, incompatibilities between mtDNA of one population and nDNA of the other could result in low fitness of hybrids. In northwestern North America, two hybridizing species of warblers, Setophaga occidentalis (abbreviated as SOCC) and S. townsendi (STOW), provide an excellent system to investigate the potential co-adaptation of mitochondrial and nuclear DNA. The inland population of STOW (inland STOW) harbors mtDNA haplotype that is half a million years divergent from the SOCC mtDNA, and these populations also differ strongly in a few nDNA regions. Coastal populations of STOW (coastal STOW) have mixed ancestry, consistent with ancient hybridization of SOCC and inland STOW-like population. Of the few highly-differentiated nDNA regions between inland STOW and SOCC, one of these regions (on chromosome 5) is also differentiated between coastal STOW and inland STOW, and covaries with mtDNA among coastal STOW populations. Genes in this 1.2Mb region of chromosome 5 are associated with fatty acid oxidation and energy-related signaling transduction, both of which are closely associated with mitochondrial function. This chromosome 5 region is correlated with mtDNA haplotypes both within and across sampling sites, a pattern consistent with mitonuclear co-adaptation. We show that such mitonuclear coevolution might be maintained by climate-related selection, because mitonuclear ancestry is correlated with climatic conditions among sampling sites. Together, our observation suggests climatic-associated adaptation shaping mitonuclear differentiation and introgression in this species complex.

evolutionary biology