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Restricted elevational ranges are common across tropical montane species, but the mechanisms generating and maintaining these patterns remain poorly resolved. A long-standing hypothesis is that specialized thermal physiology explains these distributions. However, biotic factors such as habitat and interspecific competition have also been proposed to limit tropical species’ elevational ranges. We combined point-level abundances, respirometry-based measurements of metabolic rate, habitat surveys and playback experiments to simultaneously test these three hypotheses for four species of Central American cloud forest songbirds. Contrary to the physiological hypothesis, we found no evidence that thermoregulatory costs constrain species distributions. Instead, thermal conditions across each species’ elevational range remained well within sustainable limits, staying ≤65% of hypothesized thresholds for tropical birds, even at the highest elevations. By contrast, we found some support for a combined role of habitat and competition in shaping elevational ranges. In one related species pair, the dominant lower-elevation species appears restricted by microhabitat, while the higher-elevation species is likely prevented from expanding downslope by the presence of this congener. Taken together, we conclude that thermoregulatory costs are an inadequate explanation for elevational range limits of tropical birds at our site and suggest that biotic factors can be key in shaping these distributions. We provide a Spanish translation of the Abstract in the supplementary materials. 

Abstract Despite tremendous efforts in the past decades, relationships among main avian lineages remain heavily debated without a clear resolution. Discrepancies have been attributed to diversity of species sampled, phylogenetic method and the choice of genomic regions^1–3. Here we address these issues by analysing the genomes of 363 bird species⁴(218 taxonomic families, 92% of total). Using intergenic regions and coalescent methods, we present a well-supported tree but also a marked degree of discordance. The tree confirms that Neoaves experienced rapid radiation at or near the Cretaceous–Palaeogene boundary. Sufficient loci rather than extensive taxon sampling were more effective in resolving difficult nodes. Remaining recalcitrant nodes involve species that are a challenge to model due to either extreme DNA composition, variable substitution rates, incomplete lineage sorting or complex evolutionary events such as ancient hybridization. Assessment of the effects of different genomic partitions showed high heterogeneity across the genome. We discovered sharp increases in effective population size, substitution rates and relative brain size following the Cretaceous–Palaeogene extinction event, supporting the hypothesis that emerging ecological opportunities catalysed the diversification of modern birds. The resulting phylogenetic estimate offers fresh insights into the rapid radiation of modern birds and provides a taxon-rich backbone tree for future comparative studies.