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Duffin, P. J.

Publications and source records attributed to Duffin, P. J..

3 recordsLinked to original sources

Limited neutral and adaptive genomic divergence suggests Acropora cervicornis can be managed as a single conservation unit across its range

Genomic signatures can provide key insight into the evolutionary history and remaining adaptive potential of threatened populations. As demographic decline erodes both diversity and the processes maintaining it, understanding how remaining variation is distributed becomes increasingly important for conserving species like the staghorn coral, Acropora cervicornis, a foundational but critically endangered Caribbean reef-builder. We analyzed 46 high-coverage A. cervicornis genomes from 10 locations across the tropical western Atlantic to evaluate neutral and adaptive structure, genomic diversity, demographic history, inbreeding, and connectivity, and generated a regional haplotype reference panel for future genomic monitoring. Genome-wide analyses recovered recurring regional substructure, but differentiation was modest and partly explained by isolation-by-distance and spatial variation in effective migration. Subpopulations had similar levels of genomic diversity, shared demographic history, and limited evidence of local adaptation. These patterns support interpreting sampled Caribbean populations as a single evolutionarily significant unit (ESU) containing multiple regional management units (MUs), rather than as deeply divergent evolutionary lineages. Despite substantial retained variation and low current inbreeding, estimated contemporary effective population size was small, suggesting an increased vulnerability to the effects of drift as demographic collapse continues, especially if structure is reinforced by isolated management. Together, our findings emphasize the urgent need for interventions that preserve and enhance genomic diversity, including risk-managed assisted gene flow. Supported by the haplotype reference panel developed here, these strategies will require coordinated efforts across regional entities to conserve and restore A. cervicornis as a jointly managed, single ESU.

genomics↗

Genomic separation of Salish Sea and Pacific outer coast populations of the keystone sea star Pisaster ochraceus

Understanding dispersal and population structure in marine species is critical to forecasting ecological responses to climate change. The ochre sea star (Pisaster ochraceus), an intertidal keystone predator along the North American Pacific coast, has long been considered to have little spatial genetic structure due to its extended larval dispersal period and thus high potential for gene flow. Here we characterize the spatial genomic architecture of P. ochraceus using whole-genome sequencing (WGS) data from individuals spanning over 3,000km of coastline from Alaska to southern California. Our analyses of putatively neutral SNPs evince considerable mixing throughout the latitudinal range yet reveal substantial population structure between outer Pacific coast populations and those residing within the semi-enclosed estuary of the Salish Sea, suggesting restricted gene flow and demographic divergence between these regions. Genomic divergence is further supported by evidence of selection, with outlier loci highlighting extended regions of low diversity in the Salish Sea, consistent with recent selective sweeps and potential local adaptation to the distinct estuarine conditions. These findings are consistent with the role of oceanographic barriers or environmental heterogeneity in shaping population structure in P. ochraceus, challenging an earlier notion of range-wide homogeneity. By exploring neutral and adaptive genetic diversity in this keystone marine species, we provide valuable insights for its capacity to persist in a rapidly changing world.

evolutionary biology↗

Re-evaluation of homozygous lethality for EF1A indel polymorphism in Pisaster ochraceus

A genotypic polymorphism in the sea star Pisaster ochraceus has been associated with possible overdominant maintenance of diversity, and subsequent studies of this polymorphism suggested that intermittent disease outbreaks could be a driving factor in this system. However, comparative transcriptomic studies of individuals carrying distinct genotypes at the elongation factor 1-alpha (EF1A) region indicated that the marker was not accurately describing the constitutive differences among individuals. Here we more thoroughly assess this EF1A intron region to better understand how polymorphic diversity could be associated with differential disease outcomes and physiological responses, and find that the underlying genetic model is incorrect. In fact, rather than an instance of homozygous lethality, it is clear that previous genotyping efforts were misled by a PCR artefact. We reanalyze results from two previous studies to show that the effects are not as clear as believed.

evolutionary biology↗