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Urquhart-Cronish, M.

Publications and source records attributed to Urquhart-Cronish, M..

4 recordsLinked to original sources

The historical biogeography of range expansion predicts spatial patterns in reproductive assurance

Plant reproductive assurance describes the ability of a plant to successfully reproduce in an environment that is potentially devoid of conspecifics and/or pollinators. Traditionally, studies have focused on the role of contemporary ecology---such as pollinator or mate availability---in driving spatial patterns in reproductive assurance within species, however, historical processes such as post-glacial range expansion may be an understudied alternative explanation for geographic variation in mating system. This is because during the process of geographic range expansion into novel habitat, selection should favour individuals that possess traits promoting reproductive assurance (i.e., autonomous selfing or clonal reproduction). Here, we used Northern pink monkeyflower--Erythranthe (Mimulus lewisii--a hermaphroditic, self-compatible, perennial, alpine plant, as a focal species to investigate the historical signatures of geographic range expansion by combining phylogeographic analyses with a greenhouse survey of range-wide reproductive assurance. First, we detected significant geographic variation among populations in two components of reproductive assurance: self-fertilization and clonal propagation. Next, using genome-wide single nucleotide polymorphism (SNP) data, we identified three distinct genetic clusters structured by longitude and estimated geographic coordinates of the most likely origins of range expansion within each cluster. We found that both measures of reproductive assurance significantly increased on average with distance from the inferred biogeographic origin, which is consistent with the hypothesis that reproductive assurance undergoes adaptive evolution during range expansion. This study supports hypotheses underlying Bakers Law and contributes to our understanding of spatial variation in reproductive assurance, which is linked to variation in evolutionary potential, adaptability, and the long-term persistence of populations across large spatial scales. Lay summaryWhat generates and maintains the amazing diversity in plant reproduction we see today? Traditionally, studies have focused on the role of contemporary ecology, such as pollinator or mate availability, in driving spatial patterns within species, however, historical drivers may be an understudied alternative explanation. Here, we test the hypothesis that expansion into new habitats after glacial retreat, where pollinators or mates were scarce, favors plants with the ability to reproduce in the absence of pollinators and mates by making self-pollinated seeds or vegetative clones of themselves. We find support for the hypothesis, where the probabilities of making both autonomously selfed seed and clonal vegetative propagules increase on average along inferred pathways of range expansion. Our study joins a handful of previous studies that tested and provided support for historical range expansion shaping range-wide spatial variation in reproductive assurance in plants, suggesting post-glacial range expansion may be a common mechanism creating diversity in plant mating systems.

evolutionary biology↗

An alpine plant shows no decrease in genetic diversity associated with rapid post-glacial range expansion

While range expansion is hypothesized to be a mechanism for species persistence under climate change, many eco-evolutionary models describe demographic and genetic processes during range expansion that may decrease genetic variation and increase genetic load at the leading edge (i.e., expansion load). These predictions are related to dispersal limitation at the leading edge driving colonization dynamics, a scenario common in post-glacial range expansion at the continental scale ([~]20,000 years ago). However, post-glacial range expansion can also occur on contemporary time scales, such as alpine glacier recession following the end of The Little Ice Age ([~]150 years ago) and our understanding of dispersal limitation structuring these instances of rapid range expansion are relatively understudied. Here, we test whether there is evidence supporting the role of dispersal limitation during range expansion following alpine glacier retreat using the native alpine plant Erythranthe (Mimulus) lewisii by examining patterns of neutral genetic diversity (single nucleotide polymorphisms) across the history of glacier recession (i.e., glacier chronosequence) across two glacier forelands in Garibaldi Provincial Park, BC. We find weak support for the prediction of increasing clines in genetic differentiation towards the range edge, and no support for decreasing clines in genetic diversity, suggesting dispersal limitation is not characterizing colonization during range expansion, with the implication that the accumulation of expansion load at the range edge is likely not applicable on these spatiotemporal scales. Together, our results suggest that loss of genetic diversity for range-shifting species in the alpine is likely not a key contributing factor to any decreased fitness over time.

evolutionary biology↗

Density-dependent selection during range expansion affects expansion load in life-history traits

Models of range expansion have independently explored fitness consequences of life-history trait evolution and increased rates of genetic drift--or "allele surfing"--during spatial spread, but no previous model has examined the interactions between these two processes. Here, we explore an ecologically complex range expansion scenario that combines density-dependent selection with allele surfing, using spatially explicit simulations to asses the genetic and fitness consequences of density-dependent selection on the evolution of life-history traits. We demonstrate that density-dependent selection on the range edge acts differently depending on the life-history trait and can either diminish or enhance allele surfing. Specifically, we show that selection on the range edge is always weaker at sites affecting competitive ability (K-selected traits) than intrinsic growth rate ((r-selected traits). We then link differences in the frequency of deleterious mutations to differences in the efficacy of selection and rate of mutation accumulation across distinct life-history traits. Finally, we demonstrate the fitness consequences of accumulated deleterious mutations for different life-history traits are related to the population density in which they are expressed. Our work highlights the complex relationship between ecology and expressed genetic load, which will be important to consider when interpreting both experimental and field studies of range expansion.

evolutionary biology↗

Patterns, predictors, and consequences of dominance in hybrids

Are first-generation (F1) hybrids typically intermediate for all traits that differentiate their parents? Or are they similar to one parent for most traits, or even mismatched for divergent traits? Although the phenotype of otherwise viable and fertile hybrids determines their fate, little is known about the general patterns, predictors, and consequences of phenotype expression in hybrids. To address this empirical gap, we compiled data from nearly 200 studies where traits were measured in a common environment for two parent populations and F1 hybrids. We find that individual traits are typically halfway between the parental midpoint and one parental value (i.e., hybrid trait values are typically 0.25 or 0.75 if parents values are 0 & 1). When considering pairs of traits together, a hybrids multivariate phenotype tends to resemble one parent (pairwise parent-bias) about 50 % more than the other while also exhibiting a similar magnitude of trait mismatch due to different traits having dominance in conflicting directions. We detect no phylogenetic signal nor an effect of parental genetic distance on dominance or mismatch. Using data from an experimental field planting of recombinant hybrid sunflowers--where there is among-individual variation in dominance and mismatch due to segregation of divergent alleles--we illustrate that pairwise parent-bias improves fitness while mismatch reduces fitness. Importantly, the effect of mismatch on fitness was stronger than that of pairwise parent-bias. In sum, our study has three major conclusions. First, hybrids between ecologically divergent natural populations are typically not phenotypically intermediate but rather exhibit substantial mismatch while also resembling one parent more than the other. Second, dominance and mismatch are likely determined by population-specific processes rather than general rules. Finally, selection against hybrids likely results from both selection against somewhat intermediate phenotypes and against mismatched trait combinations.

evolutionary biology↗