AI Article Synopsis

  • - The study explores how new plant species evolve through reproductive isolation and local adaptation, using the peat moss genus Sphagnum as a model system, particularly focusing on two closely related species in North America.
  • - Researchers used whole genome sequencing to analyze genetic differences between northern S. diabolicum and southern S. magniae, finding distinct genomic areas indicating evolutionary divergence tied to environmental factors.
  • - The findings suggest that the genomic differentiation observed is linked to local adaptations to different climatic zones, providing new insights into the speciation process in plants.

Article Abstract

Background And Aims: New plant species can evolve through the reinforcement of reproductive isolation via local adaptation along habitat gradients. Peat mosses (Sphagnaceae) are an emerging model system for the study of evolutionary genomics and have well-documented niche differentiation among species. Recent molecular studies have demonstrated that the globally distributed species Sphagnum magellanicum is a complex of morphologically cryptic lineages that are phylogenetically and ecologically distinct. Here, we describe the architecture of genomic differentiation between two sister species in this complex known from eastern North America: the northern S. diabolicum and the largely southern S. magniae.

Methods: We sampled plant populations from across a latitudinal gradient in eastern North America and performed whole genome and restriction-site associated DNA sequencing. These sequencing data were then analyzed computationally.

Key Results: Using sliding-window population genetic analyses we find that differentiation is concentrated within 'islands' of the genome spanning up to 400 kb that are characterized by elevated genetic divergence, suppressed recombination, reduced nucleotide diversity and increased rates of non-synonymous substitution. Sequence variants that are significantly associated with genetic structure and bioclimatic variables occur within genes that have functional enrichment for biological processes including abiotic stress response, photoperiodism and hormone-mediated signalling. Demographic modelling demonstrates that these two species diverged no more than 225 000 generations ago with secondary contact occurring where their ranges overlap.

Conclusions: We suggest that this heterogeneity of genomic differentiation is a result of linked selection and reflects the role of local adaptation to contrasting climatic zones in driving speciation. This research provides insight into the process of speciation in a group of ecologically important plants and strengthens our predictive understanding of how plant populations will respond as Earth's climate rapidly changes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666999PMC
http://dx.doi.org/10.1093/aob/mcad104DOI Listing

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