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Abstract
How do species adapt to their environments? This question has been a major driver ofevolutionary genetics research for a century. Developing cost-efficient models to address how
traits are shaped by their environments and how species adapt to distinct ecological niches is
critical as the impact of human influence on the environment becomes clearer. This dissertation
develops the use of the wine yeast Lachancea thermotolerans as a model for population
genomics by investigating the phylogenetics, population history, and phenotypic variation within
the species. Firstly, I summarized population structure using over 300 genome sequences from
strains with a broad range of geographic and environmental origins. Expansion of available
genomic resources to include 90 more isolates from European and North American woodland
habitats across two continents revealed several new tree-associated lineages. Additionally, I
found evidence for recent gene flow between continents, providing a more complete view of
population structure and the impact of environment on genetic variation. The addition of wild
strains suggested that copy number variation previously associated with adaptation to domestic
environments may be more prevalent across ecological and geographical origins than previously
thought. Secondly, analysis of growth rates at a range of temperatures showed natural genetic
variation within L. thermotolerans. Strains from one North American lineage grew at a
significantly lower rate than others at high temperatures. This suggests a single change within the
species that appears maladaptive at high temperatures has occurred. The lack of adaptation seems
surprising because there was natural genetic variation in growth rates among L. thermotolerans
strains, suggesting that standing variation exists for adaptation to high temperature growth.
Population genomic analyses require high-quality data to determine differences within a species,
and the data used here did not show intraspecies contamination. This is important because, using
simulated data, I found that contamination between 5 and 10% can alter phylogenetic tree
topology and gene flow. Overall, the results presented here emphasize the importance of
screening for intra-species contamination prior to phylogenetic or population genomic work and
demonstrate the potential of L. thermotolerans as a model system to increase understanding of
the genetic mechanisms of adaptation.