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  1. Abstract Plant phenology is affected by both abiotic conditions (i.e., temperature, nitrogen enrichment, and drought) and biotic conditions (i.e., species diversity). The degree of spatial heterogeneity in soil resources is known to influence community assembly and dynamics, but the relationship between resource heterogeneity and phenology or the potentially interactive effects of soil resources on phenology are less understood. We leveraged a tallgrass prairie restoration experiment that has manipulated soil nitrogen availability and soil depth over 20 years to test the effects of environmental heterogeneity, nutrient enrichment, and potentially interactive effects of global change drivers (nutrient enrichment and a drought manipulation) on the phenology of a highly dominant prairie grass (Andropogon gerardii). We recorded the timing of major developmental stages ofA. gerardiiin plots containing four soil heterogeneity treatments (control, soil depth heterogeneity, nutrient/depth heterogeneity, and nutrient/precipitation heterogeneity). We found that the boot, first spikelet, and emerged spikelet stages ofA. gerardiioccurred earlier in treatments with greater heterogeneity of soil nitrogen, and this effect was driven by the accelerative effect of nitrogen enrichment on phenology. Reduced precipitation increased the flowering length ofA. gerardiibut did not otherwise affect developmental phenology. There were no interactive effects among any soil resource treatments on phenology. These results advance our understanding of the relationship between plant phenology and global change drivers, which is important for understanding and predicting the timing of plant resource use and the provision of resources to higher trophic levels by plants under varying levels of resource availability. 
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  2. Abstract Enhancing resilience in formerly degraded ecosystems is an important goal of restoration ecology. However, evidence for the recovery of resilience and its underlying mechanisms require long‐term experiments and comparison with reference ecosystems. We used data from an experimental prairie restoration that featured long‐term soil heterogeneity manipulations and data from two long‐term experiments located in a comparable remnant (reference) prairie to (1) quantify the recovery of ecosystem functioning (i.e., productivity) relative to remnant prairie, (2) compare the resilience of restored and remnant prairies to a natural drought, and (3) test whether soil heterogeneity enhances resilience of restored prairie. We compared sensitivity and legacy effects between prairie types (remnant and restored) and among four prairie sites that included two remnant prairie sites and prairie restored under homogeneous and heterogeneous soil conditions. We measured sensitivity and resilience as the proportional change in aboveground net primary productivity (ANPP) during and following drought (sensitivity and legacy effects, respectively) relative to average ANPP based on 4 pre‐drought years (2014–2017). In nondrought years, total ANPP was similar between remnant and restored prairie, but remnant prairie had higher grass productivity and lower forb productivity compared with restored prairie. These ANPP patterns generally persisted during drought. The sensitivity of total ANPP to drought was similar between restored and remnant prairie, but grasses in the restored prairie were more sensitive to drought. Post‐drought legacy effects were more positive in the restored prairie, and we attributed this to the more positive and less variable legacy response of forb ANPP in the restored prairie, especially in the heterogeneous soil treatment. Our results suggest that productivity recovers in restored prairie and exhibits similar sensitivity to drought as in remnant prairie. Furthermore, creating heterogeneity promotes forb productivity and enhances restored prairie resilience to drought. 
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  3. null (Ed.)
  4. Anderson, Marti (Ed.)
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  7. 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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