Hurme, K. | Search bioRxiv

bioRxiv2026

Pauses in a fast-paced life: Intermittent hovering in hummingbirds

Hummingbirds are known for sustained hovering powered by rapid and continuous wingbeats. Here, we describe and quantify a novel flight behavior, intermittent hovering, in which hovering hummingbirds momentarily pause their wing motion mid-air but maintain their vertical position in space, keeping their wings fully extended at the end of the upstroke. We present the first systematic account of flap-pauses and wing coloration across hummingbirds, and evaluate potential morphological and ecological correlates, as well as evolutionary patterns in the expression of this behavior. Slow-motion footage from 86 species spanning all nine major hummingbird clades shows that at least 45 species exhibited flap-pauses during sustained hovering. Phylogenetic comparative analyses revealed that hovering pauses are evolutionarily conserved and significantly associated with both greater body mass and longer wings. Furthermore, we found that the 16 species in our study with colored underwings also exhibit significantly longer wings. The convergence of intermittent hovering, wing elongation, and chromatic traits leads us to hypothesize that this flight behavior plays a role in visual and/or auditory communication.

evolutionary biology↗

bioRxiv2024

Upper bill bending as an adaptation for nectar feeding in hummingbirds

Observations of maxillary (upper bill) bending in hummingbirds have been considered an optical illusion, yet a recent description of out-of-phase opening and closing between their bill base and tip suggests a genuine capacity for bill bending. We investigate bill kinematics during nectar feeding in six species of hummingbirds. We employed geometric morphometrics to identify bending zones and combined these data with measurements of bill flexural rigidity from microCT scans to better understand the flexing mechanism. We found that the mandible remains in place throughout the licking cycle, while the maxilla undergoes significant shape deformation, such that the distal portion of the upper bill bends upwards. We propose that bill bending is a key component of the drinking mechanism in hummingbirds, allowing the coordination of bill function (distal wringing and basal expansion) and tongue function (raking/squeegeeing) during intraoral transport. We present a fluid analysis that reveals a combination of pressure-driven (Poiseuille) and boundary-driven (Couette) flows, which have previously been thought to represent alternative drinking mechanisms. Bill bending allows for separation of the bill tips while maintaining a tightly closed middle section of the bill, enabling nectar exploitation in long and narrow flowers that can exclude less efficient pollinators.

evolutionary biology↗