Papers by SAJENI MAHALINGAM
While producing one of the highest sustained mass-specific power outputs of any vertebrate, hover... more While producing one of the highest sustained mass-specific power outputs of any vertebrate, hovering hummingbirds must also
precisely modulate the activity of their primary flight muscles to vary wingbeat kinematics and modulate lift production. Although
recent studies have begun to explore how pectoralis (the primary downstroke muscle) neuromuscular activation and wingbeat
kinematics are linked in hummingbirds, it is unclear whether different species modulate these features in similar ways, or
consistently in response to distinct flight challenges. In addition, little is known about how the antagonist, the supracoracoideus,
is modulated to power the symmetrical hovering upstroke. We obtained simultaneous recordings of wingbeat kinematics and
electromyograms from the pectoralis and supracoracoideus in ruby-throated hummingbirds (Archilochus colubris) hovering
under the following conditions: (1) ambient air, (2) air density reduction trials, (3) submaximal load-lifting trials and (4) maximal
load-lifting trials. Increased power output was achieved through increased stroke amplitude during air density reduction and loadlifting
trials, but wingbeat frequency only increased at low air densities. Overall, relative electromyographic (EMG) intensity was
the best predictor of stroke amplitude and is correlated with angular velocity of the wingtip. The relationship between muscle
activation intensity and kinematics was independent of treatment type, indicating that reduced drag on the wings in hypodense
air did not lead to high wingtip angular velocities independently of increased muscle work. EMG bursts consistently began and
ended before muscle shortening under all conditions. During all sustained hovering, spike number per burst consistently
averaged 1.2 in the pectoralis and 2.0 in the supracoracoideus. The number of spikes increased to 2.5–3 in both muscles during
maximal load-lifting trials. Despite the relative kinematic symmetry of the hovering downstroke and upstroke, the
supracoracoideus was activated ~1ms earlier, EMG bursts were longer (~0.9ms) and they exhibited 1.6 times as many spikes per
burst. We hypothesize that earlier and more sustained activation of the supracoracoideus fibres is necessary to offset the greater
compliance resulting from the presence of the supracoracoid tendon.
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Papers by SAJENI MAHALINGAM
precisely modulate the activity of their primary flight muscles to vary wingbeat kinematics and modulate lift production. Although
recent studies have begun to explore how pectoralis (the primary downstroke muscle) neuromuscular activation and wingbeat
kinematics are linked in hummingbirds, it is unclear whether different species modulate these features in similar ways, or
consistently in response to distinct flight challenges. In addition, little is known about how the antagonist, the supracoracoideus,
is modulated to power the symmetrical hovering upstroke. We obtained simultaneous recordings of wingbeat kinematics and
electromyograms from the pectoralis and supracoracoideus in ruby-throated hummingbirds (Archilochus colubris) hovering
under the following conditions: (1) ambient air, (2) air density reduction trials, (3) submaximal load-lifting trials and (4) maximal
load-lifting trials. Increased power output was achieved through increased stroke amplitude during air density reduction and loadlifting
trials, but wingbeat frequency only increased at low air densities. Overall, relative electromyographic (EMG) intensity was
the best predictor of stroke amplitude and is correlated with angular velocity of the wingtip. The relationship between muscle
activation intensity and kinematics was independent of treatment type, indicating that reduced drag on the wings in hypodense
air did not lead to high wingtip angular velocities independently of increased muscle work. EMG bursts consistently began and
ended before muscle shortening under all conditions. During all sustained hovering, spike number per burst consistently
averaged 1.2 in the pectoralis and 2.0 in the supracoracoideus. The number of spikes increased to 2.5–3 in both muscles during
maximal load-lifting trials. Despite the relative kinematic symmetry of the hovering downstroke and upstroke, the
supracoracoideus was activated ~1ms earlier, EMG bursts were longer (~0.9ms) and they exhibited 1.6 times as many spikes per
burst. We hypothesize that earlier and more sustained activation of the supracoracoideus fibres is necessary to offset the greater
compliance resulting from the presence of the supracoracoid tendon.
precisely modulate the activity of their primary flight muscles to vary wingbeat kinematics and modulate lift production. Although
recent studies have begun to explore how pectoralis (the primary downstroke muscle) neuromuscular activation and wingbeat
kinematics are linked in hummingbirds, it is unclear whether different species modulate these features in similar ways, or
consistently in response to distinct flight challenges. In addition, little is known about how the antagonist, the supracoracoideus,
is modulated to power the symmetrical hovering upstroke. We obtained simultaneous recordings of wingbeat kinematics and
electromyograms from the pectoralis and supracoracoideus in ruby-throated hummingbirds (Archilochus colubris) hovering
under the following conditions: (1) ambient air, (2) air density reduction trials, (3) submaximal load-lifting trials and (4) maximal
load-lifting trials. Increased power output was achieved through increased stroke amplitude during air density reduction and loadlifting
trials, but wingbeat frequency only increased at low air densities. Overall, relative electromyographic (EMG) intensity was
the best predictor of stroke amplitude and is correlated with angular velocity of the wingtip. The relationship between muscle
activation intensity and kinematics was independent of treatment type, indicating that reduced drag on the wings in hypodense
air did not lead to high wingtip angular velocities independently of increased muscle work. EMG bursts consistently began and
ended before muscle shortening under all conditions. During all sustained hovering, spike number per burst consistently
averaged 1.2 in the pectoralis and 2.0 in the supracoracoideus. The number of spikes increased to 2.5–3 in both muscles during
maximal load-lifting trials. Despite the relative kinematic symmetry of the hovering downstroke and upstroke, the
supracoracoideus was activated ~1ms earlier, EMG bursts were longer (~0.9ms) and they exhibited 1.6 times as many spikes per
burst. We hypothesize that earlier and more sustained activation of the supracoracoideus fibres is necessary to offset the greater
compliance resulting from the presence of the supracoracoid tendon.