Disclosure statement:Authors have nothing to disclose.
Abstract (237) 1 2Hybridization is well recognized as a driver of speciation, yet it often remains difficult to parse 3 phylogenomically in that post-speciation gene flow frequently supersedes an ancestral signal. 4Here we examined how interactions between recombination and gene flow shaped the 5 phylogenomic landscape of red wolf to create non-random retention of introgressed ancestry. 6Our re-analyses of genomic data recapitulate fossil evidence by demonstrating red wolf was 7 indeed extant and isolated prior to more recent admixture with other North American canids. Its 8 more ancient divergence, now sequestered within low-recombinant regions on the X-9 chromosome (i.e., chromosomal 'refugia'), is effectively masked by multiple, successive waves 10 of secondary introgression that now dominate its autosomal ancestry. These interpretations are 11 congruent with more theoretical explanations that describe the manner by which introgression 12 can be localized within the genome through recombination and selection. They also tacitly 13 support the large-X effect, i.e., the manner by which loci that contribute to reproductive isolation 14 can be enriched on the X-chromosome. By contrast, similar, high recombinant regions were also 15 found as enriched within very shallow gene trees, thus reflecting post-speciation gene flow and a 16 compression of divergence estimates to 1/20 th of that found in recombination 'cold spots'. Our 17 results effectively reconcile conflicting hypotheses regarding the impact of hybridization on 18 evolution of North American canids and support an emerging framework within which the 19 analysis of a phylogenomic landscape structured by recombination can be used to successfully 20 address the macroevolutionary implications of hybridization. 21 22 23 24 precede introgression) can be depleted, and especially so in those lineages with a history of 48 secondary introgression. However, the parsing of genealogical histories is dependent on the 49 interactions between recombination, genetic drift, and selection (McGaugh et al. 2012; Schumer 50 et al. 2018). As such, branching patterns are often retained non-randomly, with reduced 51 permeability to gene flow found in those genomic areas with low recombination, where 52 introgression of deleterious alleles is restricted by an increased efficacy of linked selection 53 (Payseur and Rieseberg 2016; Runemark et al. 2018; Schumer et al. 2018). 54The interaction between selection and recombination through time allows fundamental 55 predictions to be made with regard to the stability of hybrids genomes, and this may promote the 56 role that hybridization plays in a given lineage. In the generations following a hybridization 57 event, recombination creates junction-points where ancestries transition from one parental 58 genome to another (Fisher 1954). Their densities along the length of a chromosome can be used 59 to find loci relating to hybrid fitness, because selection against incompatible loci w...