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Concurrent invasions of European starlings in Australia and North America reveal population‐specific differentiation in shared genomic regions

Natalie R. Hofmeister; Katarina C. Stuart; Wesley C. Warren; Scott J. Werner; Melissa Bateson; Gregory F. Ball; Katherine L. Buchanan; David W. Burt; Adam P. A. Cardilini; Phillip Cassey; Tim De Meyer; Julia George; Simone L. Meddle; Hannah M. Rowland; Craig D. H. Sherman; William B. Sherwin; Wim Vanden Berghe; Lee Ann Rollins; David F. Clayton
Molecular Ecology · Vol. 34, Issue 14 · 2025

Abstract

A species' success during the invasion of new areas hinges on an interplay between the demographic processes common to invasions and the specific ecological context of the novel environment. Evolutionary genetic studies of invasive species can investigate how genetic bottlenecks and ecological conditions shape genetic variation in invasions, and our study pairs two invasive populations that are hypothesized to be from the same source population to compare how each population evolved during and after introduction. Invasive European starlings ( Sturnus vulgaris ) established populations in both Australia and North America in the 19th century. Here, we compare whole‐genome sequences among native and independently introduced European starling populations to determine how demographic processes interact with rapid evolution to generate similar genetic patterns in these recent and replicated invasions. Demographic models indicate that both invasive populations experienced genetic bottlenecks as expected based on invasion history, and we find that specific genomic regions have differentiated even on this short evolutionary timescale. Despite genetic bottlenecks, we suggest that genetic drift alone cannot explain differentiation in at least two of these regions. The demographic boom intrinsic to many invasions as well as potential inversions may have led to high population‐specific differentiation, although the patterns of genetic variation are also consistent with the hypothesis that this infamous and highly mobile invader adapted to novel selection (e.g., extrinsic factors). We use targeted sampling of replicated invasions to identify and evaluate support for multiple, interacting evolutionary mechanisms that lead to differentiation during the invasion process.

Bibliographic Information

JournalMolecular Ecology
PublisherWiley
Publication Date2025-07-01
Publication Year2025
Volume34
Issue14
Document TypeJournal Article
Print ISSN0962-1083
eISSN1365-294X
DOI10.1111/mec.17195
SubjectEcology & Organismal Biology

Access Information

NARA Access Coverage1997-01-01~Current
Journal Homepagehttps://onlinelibrary.wiley.com/loi/1365294X
Publisher PageOpen Publisher Page
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