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ABSTRACT Human disturbance can have profound effects on biodiversity, including increasing hybridization between reproductively isolated species. One approach for understanding how human activity affects hybridization dynamics is to evaluate correlations between disturbance (e.g., urbanisation, temperature change) and hybridization. Because variation in hybridization can also arise from historical factors unrelated to recent human disturbance, it is essential to account for population structure to avoid spurious correlations. Here, we combine environmental and high‐coverage whole‐genome resequencing data to investigate how human disturbance and population structure affect hybridization dynamics between a pair of pine sawflies adapted to different pines,Neodiprion leconteiandNeodiprion pinetum. We find thatN. leconteiandN. pinetumexhibit strikingly different patterns of population structure, which we hypothesise stem from differences in host use. We also find that recent admixture is both asymmetric and geographically variable. Linear regression analyses reveal that admixture proportion is predicted by indirect human disturbance (i.e., climate change) and not direct human disturbance (e.g., urbanisation) in bothN. leconteiandN. pinetum. Lastly, inN. pinetum, we find evidence of a spurious association between admixture and direct human disturbance that disappears when regression models account for population structure via inclusion of genetic principal component scores as covariates. Together, our data suggest that indirect human disturbance and population structure both contribute to geographic variation in admixture betweenN. leconteiandN. pinetum. Our study also highlights the importance of adequately controlling for population structure when attempting to identify environmental predictors (human disturbance‐related or not) of hybridization.
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Genetic Diversity and Population Structure in Cities Is Not Consistent Among Cosmopolitan Plant Species
ABSTRACT. Urbanisation has led to increasing homogenization of plant communities across cities. However, it is unclear whether these patterns extend to cosmopolitan plant species at the genetic level. We examined genome‐wide genetic patterns in six widespread plant species (three Poaceae and three Asteraceae) across five cities in the USA (Boston, Baltimore, Minneapolis‐St. Paul, Phoenix, and Los Angeles) using reduced‐representation sequencing. We assessed genetic structure, differentiation, and patterns of isolation by distance (IBD) and environment (IBE) to determine if species were genetically homogeneous or differentiated by city, percentage of impervious surface, or both. Most species exhibited limited population structure overall, withPoa annua(annual bluegrass),Taraxacum officinale(dandelion), andCynodon dactylon(Bermuda grass) showing no significant genetic differentiation among cities, a pattern consistent with high gene flow mediated by human activity. Notable exceptions included city‐level differences inErigeron canadensis(horseweed) andLactuca serriola(prickly lettuce), especially in Phoenix. We also observed low genetic diversity inDigitaria sanguinalis(crabgrass) from Phoenix, suggesting recent founder effects or selection via environmental filtering.Erigeron canadensis,the only native species studied, displayed stronger differentiation by city, along with significant isolation by temperature and distance. Among all species, we found no evidence for population structure by impervious surface. Our findings indicate that widespread population genetic structure patterns of cosmopolitan plants are likely to depend more on species attributes (e.g., self‐compatibility) and human‐mediated dispersal than on urbanisation per se.
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- Award ID(s):
- 1638648
- PAR ID:
- 10664681
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Molecular Ecology
- Volume:
- 35
- Issue:
- 3
- ISSN:
- 0962-1083
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript
- Journal Article:
- https://doi.org/10.1111/mec.70261
