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Accurate tree species identification through bark characteristics is essential for effective forest management, but traditionally requires extensive expertise. This study leverages artificial intelligence (AI), specifically the EfficientNet-B3 convolutional neural network, to enhance AI-based tree bark identification, focusing on northern red oak (Quercus rubra), hackberry (Celtis occidentalis), and bitternut hickory (Carya cordiformis) using the CentralBark dataset. We investigated three environmental variables—time of day (lighting conditions), bark moisture content (wet or dry), and cardinal direction of observation—to identify sources of classification inaccuracies. Results revealed that bark moisture significantly reduced accuracy by 8.19% in wet conditions (89.32% dry vs. 81.13% wet). In comparison, the time of day had a significant impact on hackberry (95.56% evening) and northern red oak (80.80% afternoon), with notable chi-squared associations (p < 0.05). Cardinal direction had minimal effect (4.72% variation). Bitternut hickory detection consistently underperformed (26.76%), highlighting morphological challenges. These findings underscore the need for targeted dataset augmentation with wet and afternoon images, alongside preprocessing techniques like illumination normalization, to improve model robustness. Enhanced AI tools will streamline forest inventories, support biodiversity monitoring, and bolster conservation in dynamic forest ecosystems. 

Abstract Forest canopy complexity (i.e., the three‐dimensional structure of the canopy) is often associated with increased species diversity as well as high primary productivity across natural forests. However, canopy complexity, tree diversity, and productivity are often confounded in natural forests, and the mechanisms of these relationships remain unclear. Here, we used two large tree diversity experiments in North America to assess three hypotheses: (1) increasing tree diversity leads to increased canopy complexity, (2) canopy complexity is positively related to tree productivity, and (3) the relationship between tree diversity and tree productivity is indirect and driven by the positive effects of canopy complexity. We found that increasing tree diversity from monocultures to mixtures of 12 species increases canopy complexity and productivity by up to 71% and 73%, respectively. Moreover, structural equation modeling indicates that the effects of tree diversity on productivity are indirect and mediated primarily by changes in internal canopy complexity. Ultimately, we suggest that increasing canopy complexity can be a major mechanism by which tree diversity enhances productivity in young forests. 

Abstract Decades of theory and empirical studies have demonstrated links between biodiversity and ecosystem functioning, yet the putative processes that underlie these patterns remain elusive. This is especially true for forest ecosystems, where the functional traits of plant species are challenging to quantify. We analyzed 74,563 forest inventory plots that span 35 ecoregions in the contiguous USA and found that in ~77% of the ecoregions mixed mycorrhizal plots were more productive than plots where either arbuscular or ectomycorrhizal fungal-associated tree species were dominant. Moreover, the positive effects of mixing mycorrhizal strategies on forest productivity were more pronounced at low than high tree species richness. We conclude that at low richness different mycorrhizal strategies may allow tree species to partition nutrient uptake and thus can increase community productivity, whereas at high richness other dimensions of functional diversity can enhance resource partitioning and community productivity. Our findings highlight the importance of mixed mycorrhizal strategies, in addition to that of taxonomic diversity in general, for maintaining ecosystem functioning in forests. 

Mounting evidence suggests that geographic ranges of tree species worldwide are shifting under global environmental changes. Little is known, however, about if and how these species’ range shifts may trigger the range shifts of various types of forests. Markowitz’s portfolio theory of investment and its broad application in ecology suggest that the range shift of a forest type could differ substantially from the range shifts of its constituent tree species. MethodsHere, we tested this hypothesis by comparing the range shifts of forest types and the mean of their constituent species between 1970–1999 and 2000–2019 across Alaska, Canada, and the contiguous United States using continent-wide forest inventory data. We first identified forest types in each period using autoencoder neural networks and K-means cluster analysis. For each of the 43 forest types that were identified in both periods, we systematically compared historical range shifts of the forest type and the mean of its constituent tree species based on the geographic centroids of interpolated distribution maps. ResultsWe found that forest types shifted at 86.5 km·decade^-1on average, more than three times as fast as the average of constituent tree species (28.8 km·decade^-1). We showed that a predominantly positive covariance of the species range and the change of species relative abundance triggers this marked difference. DiscussionOur findings provide an important scientific basis for adaptive forest management and conservation, which primarily depend on individual species assessment, in mitigating the impacts of rapid forest transformation under climate change. 

Abstract Structural diversity—the volume and physical arrangement of vegetation within the three‐dimensional (3D) space of ecosystems—is a predictor of ecosystem function that can be measured at large scales with remote sensing. However, the landscape composition and configuration of structural diversity across macrosystems have not been well described. Using a relatively recently developed method to quantify landscape composition and configuration of continuous habitat or terrain, we propose the application of gradient surface metrics (GSMs) to quantify landscape patterns of structural diversity and provide insights into how its spatial pattern relates to ecosystem function. We first applied an example set of GSMs that represent landscape heterogeneity, dominance, and edge density to Lidar‐derived structural diversity within 28 forested landscapes at National Ecological Observatory Network (NEON) sites. Second, we tested for forest type, geographic location, and climate drivers of macroscale variation in GSMs of structural diversity (GSM‐SD). Third, we demonstrated the utility of these metrics for understanding spatial patterns of ecosystem function in a case study with NDVI, a proxy of productivity. We found that GSM‐SD varied in landscapes within macrosystems, with forest type, geographic location, and climate being significantly related to some but not all metrics. We also found that dominance of high peaks of height and vertical complexity of canopy vegetation and the heterogeneity of the vertical complexity and coefficient of variation of canopy vegetation height within 120‐m patches were negatively correlated with NDVI across the 28 NEON sites. However, forest type always had a significant interaction term between these GSM‐SD and NDVI relationships. Our study demonstrates that GSMs are useful to describe the landscape composition and configuration of structural diversity and its relationship with productivity that warrants further consideration for spatially motivated management decisions. 

Structural diversity, characterizing the volumetric capacity and physical arrangement of biotic components in an ecosystem, controls critical ecosystem functions like light interception, hydrology, and microclimate. This product generates structural diversity metrics for the NEON sites, sourced from the Discrete-Return LiDAR Point Cloud from the NEON Aerial Observation Platform (DP1.30003.001; collected in March 2023). Using R programming, we computed the metrics detailing height, heterogeneity, and density at 30 m, aligned to the Landsat grids, for 243 site years in 57 NEON sites from 2013 to 2022.