Balancing mechanics and metabolism: elevational variation in the microanatomy of hummingbird flight muscle

Factors varying along elevational gradients impose strong aerodynamic and physiological constraints on powered flight, yet the internal anatomical correlates of flight performance in animals under such conditions remain poorly understood. In hummingbirds, sustained hovering requires extreme muscular power output, making the pectoralis muscle a key interface between environmental constraint and performance. We tested whether elevation is associated with variation in pectoralis microanatomy across three hummingbird assemblages spanning a [~]1500 m gradient in the Colombian Andes. Using tissue morphometry of trichrome-stained transverse sections of the pectoralis, we measured interstitial collagen fraction as a proxy for extracellular matrix investment and quantified fiber cross-sectional area, packing density, and size heterogeneity. Collagen investment varied across elevational bands, peaking at mid elevation ([~]1750 m) and declining toward high elevation ([~]2600 m). In contrast, muscle fibers were smaller and more densely packed at higher elevations. Variation among species was small relative to differences among elevational assemblages. Formal model comparisons provided limited support for non-linear responses to elevation, indicating that patterns across traits are better explained by interacting constraints than by a single monotonic response to factors varying along elevational gradients. These results show that hummingbird flight muscle microanatomy varies with elevation in a trait-specific manner, with the strongest evidence in fiber geometry. More broadly, our findings highlight that multiple components of muscle microarchitecture, including the extracellular matrix, vary in a context-dependent manner across elevational gradients in an extreme volant system.