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Abstract Populations along steep environmental gradients are subject to differentiating selection that can result in local adaptation, despite countervailing gene flow, and genetic drift. In montane systems, where species are often restricted to narrow ranges of elevation, it is unclear whether the selection is strong enough to influence functional differentiation of subpopulations differing by a few hundred meters in elevation. We used targeted capture of 12 501 exons from across the genome, including 271 genes previously implicated in altitude adaptation, to test for adaptation to local elevations for 2 highland hummingbird species, Coeligena violifer (n = 62) and Colibri coruscans (n = 101). For each species, we described population genetic structure across the complex geography of the Peruvian Andes and, while accounting for this structure, we tested whether elevational allele frequency clines in single nucleotide polymorphisms (SNPs) showed evidence for local adaptation to elevation. Although the 2 species exhibited contrasting population genetic structures, we found signatures of clinal genetic variation with shifts in elevation in both. The genes with SNP-elevation associations included candidate genes previously discovered for high-elevation adaptation as well as others not previously identified, with cellular functions related to hypoxia response, energy metabolism, and immune function, among others. Despite the homogenizing effects of gene flow and genetic drift, natural selection on parts of the genome evidently optimizes elevation-specific cellular function even within elevation range-restricted montane populations. Consequently, our results suggest local adaptation occurring in narrow elevation bands in tropical mountains, such as the Andes, may effectively make them “taller” biogeographic barriers. 

The seasonal movement of animals has been linked to seasonal variation in ecological productivity, and it has been hypothesized that primary consumers synchronize migration with vegetation phenology. Within temperate regions of the Northern Hemisphere, herbivorous bird species often track the phenology of vegetation greenness during spring migration. Phenological synchronization with vegetation greenness by migratory birds in other dietary guilds, across the full extent of their annual distributions during both spring and autumn migration, has not been explored.

Here, we document population‐level associations with a remotely sensed measure of vegetation greenness for 230 North American migratory bird species in seven dietary guilds across the full annual cycle using eBird occurrence information for the combined period 2006–2018.

Evidence of phenological synchronization was strongest for omnivores, herbivores, herbivore–granivores and granivores during spring and autumn migration, except for omnivores in the west during spring migration. Strong evidence of synchronization was also observed for insectivores during spring migration and carnivores during spring and autumn migration that migrated across the entire breadth of the continent. The level of evidence declined for insectivores in the west and east during spring migration, and for nectarivores in the west during spring and autumn migration. Limited evidence was also found for insectivores in the east during autumn migration, insectivores in the west and the centre of the continent during spring and autumn migration, and carnivores in the west during spring migration. Carnivores in the west during autumn migration showed the weakest evidence of synchronization.

We found broad support across an array of dietary guilds for phenological coupling between vegetation greenness and seasonal bird migration within North America. Our results highlight the potential for many migratory bird species to encounter phenological mismatches as vegetation phenology responds to climate change. Our findings emphasize the need to better understand the environmental cues that regulate migratory behaviour across dietary guilds, consumer levels and migration tactics.

 

Abstract High-elevation organisms experience shared environmental challenges that include low oxygen availability, cold temperatures, and intense ultraviolet radiation. Consequently, repeated evolution of the same genetic mechanisms may occur across high-elevation taxa. To test this prediction, we investigated the extent to which the same biochemical pathways, genes, or sites were subject to parallel molecular evolution for 12 Andean hummingbird species (family: Trochilidae) representing several independent transitions to high elevation across the phylogeny. Across high-elevation species, we discovered parallel evolution for several pathways and genes with evidence of positive selection. In particular, positively selected genes were frequently part of cellular respiration, metabolism, or cell death pathways. To further examine the role of elevation in our analyses, we compared results for low- and high-elevation species and tested different thresholds for defining elevation categories. In analyses with different elevation thresholds, positively selected genes reflected similar functions and pathways, even though there were almost no specific genes in common. For example, EPAS1 (HIF2α), which has been implicated in high-elevation adaptation in other vertebrates, shows a signature of positive selection when high-elevation is defined broadly (>1,500 m), but not when defined narrowly (>2,500 m). Although a few biochemical pathways and genes change predictably as part of hummingbird adaptation to high-elevation conditions, independent lineages have rarely adapted via the same substitutions.