Caitlin Miller

and 13 more

Identifying genetic conservation units (CUs) in threatened species is critical for the preservation of adaptive capacity and evolutionary potential in the face of climate change. However, delineating CUs in highly mobile species remains a challenge due to high rates of gene flow and genetic signatures of isolation by distance. Even when CUs are delineated in highly mobile species, the CUs often lack key biological information about what populations have the most conservation need to guide management decisions. Here we implement a framework for rigorous CU identification in the Canada Warbler (Cardellina canadensis), a highly mobile migratory bird species of conservation concern, and then integrate demographic modeling and genomic offset within a CU framework to guide conservation decisions. We find that whole-genome structure in this highly mobile species is primarily driven by putative adaptive variation. Identification of CUs across the breeding range revealed that Canada Warblers fall into two Evolutionarily Significant Units (ESU), and three putative Adaptive Units (AUs) in the South, East and Northwest. Quantification of genomic offset within each AU reveals significant spatial variation in climate vulnerability, with the Northwestern AU being identified as the most vulnerable to future climate change based on genomic offset predictions. Alternatively, quantification of past population trends within each AU revealed the steepest population declines have occurred within the Eastern AU. Overall, we illustrate that genomics-informed CUs provide a strong foundation for identifying current and potential future regional threats that can be used to manage highly mobile species in a rapidly changing world.

Matthew DeSaix

and 14 more

Matthew DeSaix

and 3 more

Low-coverage whole genome sequencing (WGS) is increasingly used for the study of evolution and ecology in both model and non-model organisms; however, effective application of low-coverage WGS data requires the implementation of probabilistic frameworks to account for the uncertainties in genotype likelihood data. Here, we present a probabilistic framework for using genotype likelihood data for standard population assignment applications. Additionally, we derive the Fisher information for allele frequency from genotype likelihood data and use that to describe a novel metric, the effective sample size, which figures heavily in assignment accuracy. We make these developments available for application through WGSassign, an open-source software package that is computationally efficient for working with whole genome data. Using simulated and empirical data sets, we demonstrate the behavior of our assignment method across a range of population structures, sample sizes, and read depths. Through these results, we show that WGSassign can provide highly accurate assignment, even for samples with low average read depths (< 0.01X) and among weakly differentiated populations. Our simulation results highlight the importance of equalizing the effective sample sizes among source populations in order to achieve accurate population assignment with low-coverage WGS data. We further provide study design recommendations for population-assignment studies and discuss the broad utility of effective sample size for studies using low-coverage WGS data.