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Tobias, Z. J. C.

Publications and source records attributed to Tobias, Z. J. C..

2 recordsLinked to original sources

A distributed genomic architecture of repeated thermal adaptation in a low-dispersal marine invader

The repeatability of the genomic basis of adaptation depends on both genetic architecture and demographic history. Understanding this repeatability, and therefore the predictability of evolution, is increasingly important under global environmental change. Biological invasions are themselves a major component of global change and provide natural experiments for testing rapid adaptation and genomic parallelism across independently invaded ranges. The colonial ascidian Botryllus schlosseri is a widespread marine invader characterized by restricted larval dispersal and strong population structure. We used low-coverage whole-genome sequencing of 532 B. schlosseri individuals from 24 populations across North America to test for repeated thermal adaptation across the Atlantic and Pacific coasts. Genotype-environment association analyses identified thousands of loci associated with temperature in divergent lineages on either coast. Although most significant SNPs, genomic windows, and genes were lineage-specific, cross-lineage overlap exceeded null expectations, revealing a modest but detectable repeated component of putative thermal adaptation. Temperature-associated variation was broadly distributed across the genome. Regions with distinctive local population structure, potentially reflecting linked haplotypic structure or reduced recombination, showed modest enrichment for genotype-environment associations, particularly in the Pacific lineage, but did not disproportionately contain the parallel component of the response. Together, these results suggest that rapid thermal adaptation in B. schlosseri is partially repeatable despite deep divergence, but is largely distributed across the genome rather than concentrated within a few tightly linked regions. Restricted migration may therefore permit locally adaptive variants to evolve more independently across the genome, reducing the importance of concentrated genomic architectures favored under stronger migration-selection conflict.

evolutionary biology↗

Evolutionary constraint predicts the repeatability of transcriptional divergence during repeated adaptation

The repeated evolution of similar phenotypes in response to shared ecological pressures provides striking examples of natural selection and raises broader questions about the predictability of evolution. Evolutionary constraint may shape this predictability, while the apparent extent of parallelism may also depend on the biological scale at which it is measured. When are adaptive solutions channeled along the same route? We addressed this question using three sympatric benthic-limnetic ecotype pairs of threespine stickleback (Gasterosteus aculeatus), characterizing gene expression in gill and liver from wild-caught fish. We tested whether proxies of pleiotropic and coding-sequence constraint predicted the repeatability of transcriptional divergence across lakes. At the gene level, differential expression was strongly biased toward parallel rather than antiparallel responses. At the functional level, numerous pathways showed parallel enrichment, but the conservation of their underlying member-gene responses varied substantially, indicating that similar functional outcomes can arise with differing degrees of gene-level concordance. Most importantly, several proxies of evolutionary constraint predicted transcriptional repeatability, particularly in gill: broadly expressed, highly connected, and more slowly evolving genes showed more stable expression responses across lakes, with similar relationships evident for repeated use of genes within functionally parallel pathways. Together, these results show that both gene-level constraint and biological scale contribute to variation in molecular repeatability and suggest that the predictability of repeated adaptation may reflect an interaction between genetic architecture, population-genetic context, and the level of biological organization at which parallelism emerges.

evolutionary biology↗