Improved tests for the origin of allometric scaling across tree architectures

The scaling of organismal metabolic rates with body size is one of the most prominent empirical patterns in biology. For over a century, the nature and causes of metabolic scaling have been the subject of much focus and debate. West, Brown, and Enquist (WBE) proposed a general model for the origin of metabolic scaling from branching vascular networks. However, recent empirical tests of WBE vascular scaling predictions in plants and animals have reported deviations caused by variability in network geometry. After clarifying the core assumptions of the WBE model, we revisit the methods and conclusions of recent tests conducted in trees, finding support for key WBE predictions in woody plant architecture. To do this, we apply an approach that better captures: i) network branching self-similarity and ii) leaf area as a proxy of plant metabolic capacity. The WBE model also predicts curvature in metabolic scaling in smaller organisms, and we introduce a novel method that accounts for curvature in plant branching geometry. Together, these advances allow more direct measurements of metabolic scaling than previous work, and we apply them to a dataset of diverse laser-scanned tree architectures. Analyses reveal the predicted interspecific ¾ metabolic scaling across tree crowns, with intraspecific variation within individual tree crowns. Scaling variability is consistent with WBE predictions for curvature from asymptotic growth and underlying variation in branching geometry. We conclude that linking fine-scale branching variation to metabolic scaling allometries remains a challenge, while our results support the foundational hypotheses of the WBE model.