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Abstract The latitudinal diversity gradient (LDG) dominates global patterns of diversity^1,2, but the factors that underlie the LDG remain elusive. Here we use a unique global dataset³to show that vascular plants on oceanic islands exhibit a weakened LDG and explore potential mechanisms for this effect. Our results show that traditional physical drivers of island biogeography⁴—namely area and isolation—contribute to the difference between island and mainland diversity at a given latitude (that is, the island species deficit), as smaller and more distant islands experience reduced colonization. However, plant species with mutualists are underrepresented on islands, and we find that this plant mutualism filter explains more variation in the island species deficit than abiotic factors. In particular, plant species that require animal pollinators or microbial mutualists such as arbuscular mycorrhizal fungi contribute disproportionately to the island species deficit near the Equator, with contributions decreasing with distance from the Equator. Plant mutualist filters on species richness are particularly strong at low absolute latitudes where mainland richness is highest, weakening the LDG of oceanic islands. These results provide empirical evidence that mutualisms, habitat heterogeneity and dispersal are key to the maintenance of high tropical plant diversity and mediate the biogeographic patterns of plant diversity on Earth. 

With increased interest in forest restoration comes an urgent need to provide accurate, scalable, and cost‐effective monitoring tools. The ubiquity of smartphones has led to a surge in monitoring apps. We reviewed and assessed monitoring apps found through web searches and conversations with practitioners. We identified 42 apps that (1) automatically monitor indicators or (2) facilitate data entry. We selected the five most promising from the first category, based on their relevance, availability, stability, and user support. We compared them to traditional field techniques in a well‐studied restoration project in Costa Rica. We received further feedback from 15 collaborator organizations that evaluated these in their corresponding field restoration sites. Diameter measurements correlated well with traditional tape‐based measurements (R² = 0.86–0.89). Canopy openness and ground cover showed weaker correlations to densiometer and quadrat cover measurements (R² = 0.42–0.51). Apps did not improve labor efficiency but do preclude the purchase of specialized field equipment. The apps reviewed here need further development and validation to support monitoring adequately, especially in the tropics. Estimates of development and maintenance costs, as well as statistics on user uptake, are required for cost‐effective development. We recommend a coordinated effort to develop dedicated restoration monitoring apps that can speed up and standardize the collection of indicators and provide evidence on restoration outcomes alongside a centralized repository of this information. 

Abstract Island biogeography has classically focused on abiotic drivers of species distributions. However, recent work has highlighted the importance of mutualistic biotic interactions in structuring island floras. The limited occurrence of specialist pollinators and mycorrhizal fungi have been found to restrict plant colonization on oceanic islands. Another important mutualistic association occurs between nearly 15,000 plant species and nitrogen-fixing (N-fixing) bacteria. Here, we look for evidence that N-fixing bacteria limit establishment of plants that associate with them. Globally, we find that plants associating with N-fixing bacteria are disproportionately underrepresented on islands, with a 22% decline. Further, the probability of N-fixing plants occurring on islands decreases with island isolation and, where present, the proportion of N-fixing plant species decreases with distance for large, but not small islands. These findings suggest that N-fixing bacteria serve as a filter to plant establishment on islands, altering global plant biogeography, with implications for ecosystem development and introduction risks. 

Abstract Substantial global attention is focused on how to reduce the risk of future pandemics. Reducing this risk requires investment in prevention, preparedness, and response. Although preparedness and response have received significant focus, prevention, especially the prevention of zoonotic spillover, remains largely absent from global conversations. This oversight is due in part to the lack of a clear definition of prevention and lack of guidance on how to achieve it. To address this gap, we elucidate the mechanisms linking environmental change and zoonotic spillover using spillover of viruses from bats as a case study. We identify ecological interventions that can disrupt these spillover mechanisms and propose policy frameworks for their implementation. Recognizing that pandemics originate in ecological systems, we advocate for integrating ecological approaches alongside biomedical approaches in a comprehensive and balanced pandemic prevention strategy. 

Wood decomposition is regulated by multiple controls, including climate and wood traits, that vary at local to regional scales. Yet decomposition rates differ dramatically when these controls do not. Fungal community dynamics are often invoked to explain these differences, suggesting that knowledge of ecosystem properties that influence fungal communities will improve understanding and projection of wood decomposition. We hypothesize that deadwood inputs decompose faster in forests with higher stocks of downed coarse woody material (CWM) because CWM is a resource from which lignocellulolytic fungi rapidly colonize new inputs. To test this hypothesis, we measure decomposition of 1,116 pieces of fine woody material (FWM) of five species, incubated for 13 to 49 months at five locations spanning 10°-latitude in eastern U.S. forest. We place FWM pieces near and far from CWM across observational transects and experimental common gardens. Soil temperature positively affects location-level mean decomposition rates, but these among-location differences are smaller than within-location variation in decomposition. Some of this variability is caused by CWM, where FWM pieces next to CWM decompose more rapidly. These effects are greater with time of incubation and lower initial wood density of FWM. The effect size of CWM is of the same relative magnitude as for the known controls of temperature, deadwood density and diameter. Abundance data for CWM is available for many forests and hence may be an ecosystem variable amenable for inclusion in decomposition models. Our findings suggest that conservation efforts to rebuild depleted CWM stocks in temperate forests may accelerate decomposition of fresh deadwood inputs. Please see the associated manuscript for the Methods. All files are in .txt or .csv format and so can be opened with common, open-source software. The file named 'README_BradfordetalCWMproximity.txt' describes the uploaded files. 

Tree growth and longevity trade-offs fundamentally shape the terrestrial carbon balance. Yet, we lack a unified understanding of how such trade-offs vary across the world’s forests. By mapping life history traits for a wide range of species across the Americas, we reveal considerable variation in life expectancies from 10 centimeters in diameter (ranging from 1.3 to 3195 years) and show that the pace of life for trees can be accurately classified into four demographic functional types. We found emergent patterns in the strength of trade-offs between growth and longevity across a temperature gradient. Furthermore, we show that the diversity of life history traits varies predictably across forest biomes, giving rise to a positive relationship between trait diversity and productivity. Our pan-latitudinal assessment provides new insights into the demographic mechanisms that govern the carbon turnover rate across forest biomes.