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In addition to changes associated with climate and land use, parrots are threatened by hunting and capture for the pet trade, making them one of the most at risk orders of birds for which conservation action is especially important. Species richness is often used to identify high priority areas for conserving biodiversity. By definition, richness considers all species to be equally different from one another. However, ongoing research emphasizes the importance of incorporating ecological functions (functional diversity) or evolutionary relationships (phylogenetic diversity) to more fully understand patterns of biodiversity, because (1) areas of high species richness do not always represent areas of high functional or phylogenetic diversity, and (2) functional or phylogenetic diversity may better predict ecosystem function and evolutionary potential, which are essential for effective long–term conservation policy and management. We created a framework for identifying areas of high species richness, functional diversity, and phylogenetic diversity within the global distribution of parrots. We combined species richness, functional diversity, and phylogenetic diversity into an Integrated Biodiversity Index (IBI) to identify global biodiversity hotspots for parrots. We found important spatial mismatches between dimensions, demonstrating species richness is not always an effective proxy for other dimensions of parrot biodiversity. The IBI is an integrative and flexible index that can incorporate multiple dimensions of biodiversity, resulting in an intuitive and direct way of assessing comprehensive goals in conservation planning. 

Abstract Aim The microbial metabolic quotient (MMQ; mg CO 2 ‐C/mg MBC/h), defined as the amount of microbial CO 2 respired (MR; mg CO 2 ‐C/kg soil/h) per unit of microbial biomass C (MBC; mg C/kg soil), is a key parameter for understanding the microbial regulation of the carbon (C) cycle, including soil C sequestration. Here, we experimentally tested hypotheses about the individual and interactive effects of multiple nutrient addition (nitrogen + phosphorus + potassium + micronutrients) and herbivore exclusion on MR, MBC and MMQ across 23 sites (five continents). Our sites encompassed a wide range of edaphoclimatic conditions; thus, we assessed which edaphoclimatic variables affected MMQ the most and how they interacted with our treatments. Location Australia, Asia, Europe, North/South America. Time period 2015–2016. Major taxa Soil microbes. Methods Soils were collected from plots with established experimental treatments. MR was assessed in a 5‐week laboratory incubation without glucose addition, MBC via substrate‐induced respiration. MMQ was calculated as MR/MBC and corrected for soil temperatures (MMQsoil). Using linear mixed effects models (LMMs) and structural equation models (SEMs), we analysed how edaphoclimatic characteristics and treatments interactively affected MMQsoil. Results MMQsoil was higher in locations with higher mean annual temperature, lower water holding capacity and lower soil organic C concentration, but did not respond to our treatments across sites as neither MR nor MBC changed. We attributed this relative homeostasis to our treatments to the modulating influence of edaphoclimatic variables. For example, herbivore exclusion, regardless of fertilization, led to greater MMQsoil only at sites with lower soil organic C (< 1.7%). Main conclusions Our results pinpoint the main variables related to MMQsoil across grasslands and emphasize the importance of the local edaphoclimatic conditions in controlling the response of the C cycle to anthropogenic stressors. By testing hypotheses about MMQsoil across global edaphoclimatic gradients, this work also helps to align the conflicting results of prior studies.