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Competition, niche differences and chance all contribute to community assembly; yet, the role of reproductive interactions between species is often less appreciated. Closely related plant species that share floral form, phenology and habitat often interact through pollination. They potentially facilitate pollinator attraction, compete for pollination services and/or exchange pollen. If reproductive processes are important to co‐occurrence, we predicted that fitness costs of heterospecific pollen transfer or pollen limitation should result in lower rates of co‐occurrence among outcrossing congeners. In contrast, selfers, which may be less exposed to heterospecific pollen, and/or less negatively affected by it, should co‐occur more frequently.Flower size is an excellent proxy for mating system in clovers. Using herbarium records and three independent field datasets, we documented co‐occurrence patterns of Trifolium at 1 m2–1 km2 scales in California. Using a randomization procedure to reshuffle matrices of community membership, we generated null hypotheses for the expected composition of large‐ and small‐flowered species in Trifolium communities of different sizes.Across all spatial scales, large‐flowered outcrossers were over‐represented at sites lacking congeners, but under‐represented in communities with multiple congeners. Conversely, small‐flowered selfers often occupied sites with multiple other Trifolium species. Patterns for plant height and leaf size, which are weakly or strongly correlated with flower size, did not explain co‐occurrence patterns as robustly. Regression analysis and model selection corroborated the null model analyses, indicating that the likelihood of co‐occurrence decreased as flower size, and thus reliance on outcrossing, increased.Synthesis. This study suggests that reproductive traits and processes may be significant contributors to community assembly and co‐occurrence in flowering plants. [ABSTRACT FROM AUTHOR]

Exotic, invasive plants and animals can wreak havoc on ecosystems by displacing natives and altering environmental conditions. However, much less is known about the identities or evolutionary dynamics of the symbiotic microbes that accompany invasive species. Most leguminous plants rely upon symbiotic rhizobium bacteria to fix nitrogen and are incapable of colonizing areas devoid of compatible rhizobia. We compare the genomes of symbiotic rhizobia in a portion of the legume's invaded range with those of the rhizobium symbionts from across the legume's native range. We show that in an area of California the legume Medicago polymorpha has invaded, its Ensifer medicae symbionts: (i) exhibit genome-wide patterns of relatedness that together with historical evidence support host-symbiont co-invasion from Europe into California, (ii) exhibit population genomic patterns consistent with the introduction of the majority of deep diversity from the native range, rather than a genetic bottleneck during colonization of California and (iii) harbor a large set of accessory genes uniquely enriched in binding functions, which could play a role in habitat invasion. Examining microbial symbiont genome dynamics during biological invasions is critical for assessing host-symbiont co-invasions whereby microbial symbiont range expansion underlies plant and animal invasions., (© FEMS 2017. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)