Cheng Bo, Tobalske Bret W, Powers Donald R, Hedrick Tyson L, Wang Yi, Wethington Susan M, Chiu George T-C, Deng Xinyan
Department of Mechanical and Nuclear Engineering, Pennsylvania State University, University Park, PA 16802, USA
Field Research Station at Fort Missoula, Division of Biological Sciences, University of Montana, Missoula, MT 59812, USA.
J Exp Biol. 2016 Nov 15;219(Pt 22):3532-3543. doi: 10.1242/jeb.137570. Epub 2016 Sep 5.
The superior manoeuvrability of hummingbirds emerges from complex interactions of specialized neural and physiological processes with the unique flight dynamics of flapping wings. Escape manoeuvring is an ecologically relevant, natural behaviour of hummingbirds, from which we can gain understanding into the functional limits of vertebrate locomotor capacity. Here, we extend our kinematic analysis of escape manoeuvres from a companion paper to assess two potential limiting factors of the manoeuvring performance of hummingbirds: (1) muscle mechanical power output and (2) delays in the neural sensing and control system. We focused on the magnificent hummingbird (Eugenes fulgens, 7.8 g) and the black-chinned hummingbird (Archilochus alexandri, 3.1 g), which represent large and small species, respectively. We first estimated the aerodynamic forces, moments and the mechanical power of escape manoeuvres using measured wing kinematics. Comparing active-manoeuvring and passive-damping aerodynamic moments, we found that pitch dynamics were lightly damped and dominated by the effect of inertia, while roll dynamics were highly damped. To achieve observed closed-loop performance, pitch manoeuvres required faster sensorimotor transduction, as hummingbirds can only tolerate half the delay allowed in roll manoeuvres. Accordingly, our results suggested that pitch control may require a more sophisticated control strategy, such as those based on prediction. For the magnificent hummingbird, we estimated that escape manoeuvres required muscle mass-specific power 4.5 times that during hovering. Therefore, in addition to the limitation imposed by sensorimotor delays, muscle power could also limit the performance of escape manoeuvres.
蜂鸟卓越的机动性源于专门的神经和生理过程与扑翼独特飞行动力学之间的复杂相互作用。逃避机动是蜂鸟一种与生态相关的自然行为,通过它我们可以了解脊椎动物运动能力的功能极限。在此,我们将之前一篇相关论文中对逃避机动的运动学分析进行拓展,以评估蜂鸟机动性能的两个潜在限制因素:(1)肌肉机械功率输出,以及(2)神经传感和控制系统中的延迟。我们重点研究了华丽蜂鸟(Eugenes fulgens,体重7.8克)和黑颏蜂鸟(Archilochus alexandri,体重3.1克),它们分别代表了大型和小型蜂鸟物种。我们首先利用测量得到的翅膀运动学数据估算了逃避机动的气动力、力矩和机械功率。通过比较主动机动和被动阻尼气动力矩,我们发现俯仰动力学的阻尼较小,主要受惯性影响,而横滚动力学的阻尼很大。为了实现观察到的闭环性能,俯仰机动需要更快的感觉运动转换,因为蜂鸟在俯仰机动中能容忍的延迟只有横滚机动的一半。因此,我们研究结果表明,俯仰控制可能需要更复杂的控制策略,比如基于预测的策略。对于华丽蜂鸟,我们估计逃避机动所需的肌肉质量比功率是悬停时的4.5倍。所以,除了感觉运动延迟带来的限制外,肌肉功率也可能限制逃避机动的性能。