Search for: All records

Abstract Researchers have long assumed that plant spatial location influences plant reproductive success and pollinator foraging behaviour. For example, many flowering plant populations have small, linear or irregular shapes that increase the proportion of plants on the edge, which may reduce mating opportunities through both male and female function. Additionally, plants that rely on pollinators may be particularly vulnerable to edge effects if those pollinators exhibit restricted foraging and pollen carryover is limited. To explore the effects of spatial location (edge vs. interior) on siring success, seed production, pollinator foraging patterns and pollen-mediated gene dispersal, we established a square experimental array of 49 Mimulus ringens (monkeyflower) plants. We observed foraging patterns of pollinating bumblebees and used paternity analysis to quantify male and female reproductive success and mate diversity for plants on the edge versus interior. We found no significant differences between edge and interior plants in the number of seeds sired, mothered or the number of sires per fruit. However, we found strong differences in pollinator behaviour based on plant location, including 15 % lower per flower visitation rates and substantially longer interplant moves for edge plants. This translated into 40 % greater pollen-mediated gene dispersal for edge than for interior plants. Overall, our results suggest that edge effects are not as strong as is commonly assumed, and that different plant reproduction parameters respond to spatial location independently. 

Abstract Variation in selfing rates within and among populations of hermaphroditic flowering plants can strongly influence the evolution of reproductive strategies and the genetic structure of populations. This intraspecific variation in mating patterns may reflect both genetic and ecological factors, but the relative importance of these factors remains poorly understood. Here, we explore how selfing in 13 natural populations of the perennial wildflowerMimulus ringensis influenced by (a) pollinator visitation, an ecological factor, and (b) floral display, a trait with a genetic component that also responds to environmental variation. We also explore whether genetically based floral traits, including herkogamy, affect selfing. We found substantial variation among populations in selfing rate (0.13–0.55). Selfing increased strongly and significantly with floral display, among as well as within populations. Selfing also increased at sites with lower pollinator visitation and low plant density. However, selfing was not correlated with floral morphology. Overall, these results suggest that pollinator visitation and floral display, two factors that interact to affect geitonogamous pollinator movements, can influence the selfing rate. This study identifies mechanisms that may play a role in maintaining selfing rate variation among populations. 

Green plants (Viridiplantae) include around 450,000–500,000 species of great diversity and have important roles in terrestrial and aquatic ecosystems. Here, as part of the One Thousand Plant Transcriptomes Initiative, we sequenced the vegetative transcriptomes of 1,124 species that span the diversity of plants in a broad sense (Archaeplastida), including green plants (Viridiplantae), glaucophytes (Glaucophyta) and red algae (Rhodophyta). Our analysis provides a robust phylogenomic framework for examining the evolution of green plants. Most inferred species relationships are well supported across multiple species tree and supermatrix analyses, but discordance among plastid and nuclear gene trees at a few important nodes highlights the complexity of plant genome evolution, including polyploidy, periods of rapid speciation, and extinction. Incomplete sorting of ancestral variation, polyploidization and massive expansions of gene families punctuate the evolutionary history of green plants. Notably, we find that large expansions of gene families preceded the origins of green plants, land plants and vascular plants, whereas whole-genome duplications are inferred to have occurred repeatedly throughout the evolution of flowering plants and ferns. The increasing availability of high-quality plant genome sequences and advances in functional genomics are enabling research on genome evolution across the green tree of life.