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Creators/Authors contains: "Grman, Emily"

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  1. Soil microbial mutualists like rhizobia bacteria can promote the establishment of rare, late‐successional legumes. Despite restoration efforts, these mutualists are often absent in the microbiome. Therefore, restoring this mutualism by directly inoculating rare legumes with rhizobia mutualists may increase plant establishment. We inoculated seedlings ofAmorpha canescens,Dalea purpurea, andLespedeza capitatawith three strains of species‐specific rhizobia each to investigate how this mutualism would promote growth in the field and in the greenhouse. Because many herbaceous plants are vulnerable to herbivory, we used exclosures for half of our field transplantations to prevent mammalian herbivory. We did not find that rhizobia bacteria directly promoted the growth of our legumes in the field but rather that herbivory and environmental conditions overwhelmed the effects of the rhizobia. Of the plants transplanted, only 17.78% of 180 survived to the end of the growing season, all of which were protected from herbivory. Survival at the end of the growing season was also greater in the northern, drier end of the field site. In the second growing season, plants were more likely to survive in the exclosure treatment, while only four recovered in the open treatment. In the greenhouse, we found increased nodulation with inoculations, supporting the hypothesis that species‐specific mutualists are absent from restoration sites. Though several recent studies have shown that restoring mutualistic interactions has the potential to dramatically improve the outcomes of ecological restoration, our results show that protecting rare species from herbivory after transplantation might achieve greater gains in establishment. 
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    Free, publicly-accessible full text available November 1, 2025
  2. Native legumes are functionally important members of grasslands, but their reintroduction into degraded systems is limited by strong establishment filters. One of these establishment filters might be rhizobia limitation, where legume seedlings are unable to find suitable rhizobia symbionts in grasslands targeted for restoration. To test links between rhizobial inoculation and legume demographic parameters in a grassland restoration context, we evaluated how inoculation with rhizobia altered survival and seed production of a native annual legume (Chamaecrista fasciculata) inoculated with rhizobia and transplanted into a restored prairie. Small mammal herbivory was an important filter affecting survival ofC. fasciculatatransplants, with inoculated plants 81% more likely to be grazed than uninoculated plants. Despite this heavy grazing, plants inoculated with rhizobia survived transplantation 71% more often and, as a result, produced 82% more flowers, experienced 73% more visits by pollinators, and on average produced 220% more seeds. Our results indicate that although herbivory may also shape legume population establishment, at least in some years in some places, rhizobia could alterC. fasciculatainteractions with both herbivores and pollinators and improve population establishment. 
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  3. Abstract In our changing world, understanding plant community responses to global change drivers is critical for predicting future ecosystem composition and function. Plant functional traits promise to be a key predictive tool for many ecosystems, including grasslands; however, their use requires both complete plant community and functional trait data. Yet, representation of these data in global databases is sparse, particularly beyond a handful of most used traits and common species. Here we present the CoRRE Trait Data, spanning 17 traits (9 categorical, 8 continuous) anticipated to predict species’ responses to global change for 4,079 vascular plant species across 173 plant families present in 390 grassland experiments from around the world. The dataset contains complete categorical trait records for all 4,079 plant species obtained from a comprehensive literature search, as well as nearly complete coverage (99.97%) of imputed continuous trait values for a subset of 2,927 plant species. These data will shed light on mechanisms underlying population, community, and ecosystem responses to global change in grasslands worldwide. 
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    Free, publicly-accessible full text available December 1, 2025
  4. Plants are subject to tradeoffs among growth strategies such that adaptations for optimal growth in one condition can preclude optimal growth in another. Thus, we predicted that a plant species that responds positively to one global change treatment would be less likely than average to respond positively to another treatment, particularly for pairs of treatments that favor distinct traits. We examined plant species abundances in 39 global change experiments manipulating two or more of the following: CO2, nitrogen, phosphorus, water, temperature, or disturbance. Overall, the directional response of a species to one treatment was 13% more likely than expected to oppose its response to a another single-factor treatment. This tendency was detectable across the global dataset but held little predictive power for individual treatment combinations or within individual experiments. While tradeoffs in the ability to respond to different global change treatments exert discernible global effects, other forces obscure their influence in local communities. 
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  5. Global change drivers (GCDs) are expected to alter community structure and consequently, the services that ecosystems provide. Yet, few experimental investigations have examined effects of GCDs on plant community structure across multiple ecosystem types, and those that do exist present conflicting patterns. In an unprecedented global synthesis of over 100 experiments that manipulated factors linked to GCDs, we show that herbaceous plant community responses depend on experimental manipulation length and number of factors manipulated. We found that plant communities are fairly resistant to experimentally manipulated GCDs in the short term (<10 y). In contrast, long-term (≥10 y) experiments show increasing community divergence of treatments from control conditions. Surprisingly, these community responses occurred with similar frequency across the GCD types manipulated in our database. However, community responses were more common when 3 or more GCDs were simultaneously manipulated, suggesting the emergence of additive or synergistic effects of multiple drivers, particularly over long time periods. In half of the cases, GCD manipulations caused a difference in community composition without a corresponding species richness difference, indicating that species reordering or replacement is an important mechanism of community responses to GCDs and should be given greater consideration when examining consequences of GCDs for the biodiversity–ecosystem function relationship. Human activities are currently driving unparalleled global changes worldwide. Our analyses provide the most comprehensive evidence to date that these human activities may have widespread impacts on plant community composition globally, which will increase in frequency over time and be greater in areas where communities face multiple GCDs simultaneously. 
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  6. Abstract Global change is impacting plant community composition, but the mechanisms underlying these changes are unclear. Using a dataset of 58 global change experiments, we tested the five fundamental mechanisms of community change: changes in evenness and richness, reordering, species gains and losses. We found 71% of communities were impacted by global change treatments, and 88% of communities that were exposed to two or more global change drivers were impacted. Further, all mechanisms of change were equally likely to be affected by global change treatments—species losses and changes in richness were just as common as species gains and reordering. We also found no evidence of a progression of community changes, for example, reordering and changes in evenness did not precede species gains and losses. We demonstrate that all processes underlying plant community composition changes are equally affected by treatments and often occur simultaneously, necessitating a wholistic approach to quantifying community changes. 
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