Gatesy Stephen M, Dial Kenneth P
Department of Biology, Wake Forest University, Winston-Salem, North Carolina, 27109.
Division of Biological Sciences, University of Montana, Missoula, Montana, 59812.
Evolution. 1996 Oct;50(5):2037-2048. doi: 10.1111/j.1558-5646.1996.tb03590.x.
Modern birds have extremely short tail skeletons relative to Archaeopteryx and nonavialian theropod dinosaurs. Long- and short-tailed birds also differ in the conformation of main tail feathers making up the flight surface: frond shaped in Archaeopteryx and fan shaped in extant fliers. Mechanisms of tail fanning were evaluated by electromyography in freely flying pigeons and turkeys and by electrical stimulation of caudal muscles in anesthetized birds. Results from these experiments reveal that the pygostyle, rectrices, rectricial bulbs, and bulbi rectricium musculature form a specialized fanning mechanism. Contrary to previous models, our data support the interpretation that the bulbi rectricium independently controls tail fanning; other muscles are neither capable of nor necessary for significant rectricial abduction. This bulb mechanism permits rapid changes in tail span, thereby allowing the exploitation of a wide range of lift forces. Isolation of the bulbs on the pygostyle effectively decouples tail fanning from fan movement, which is governed by the remaining caudal muscles. The tail of Archaeopteryx, however, differs from this arrangement in several important respects. Archaeopteryx probably had a limited range of lift forces and tight coupling between vertebral and rectricial movement. This would have made the tail of this primitive flier better suited to stabilization than maneuverability. The capacity to significantly alter lift and manipulate the flight surface without distortion may have been two factors favoring tail shortening and pygostyle development during avian evolution.
与始祖鸟和非鸟恐龙相比,现代鸟类的尾骨极其短小。长尾和短尾鸟类在构成飞行表面的主要尾羽形态上也存在差异:始祖鸟的尾羽呈叶状,而现存飞行鸟类的尾羽呈扇形。通过对自由飞行的鸽子和火鸡进行肌电图检查,以及对麻醉鸟类的尾肌进行电刺激,来评估尾羽扇动的机制。这些实验结果表明,尾综骨、尾羽、尾羽球和尾羽球肌肉组织形成了一种专门的扇动机制。与之前的模型相反,我们的数据支持这样一种解释,即尾羽球独立控制尾羽扇动;其他肌肉既无法也无需实现显著的尾羽外展。这种球机制允许尾展迅速变化,从而能够利用广泛的升力。将尾综骨上的尾羽球分离,有效地使尾羽扇动与由其余尾肌控制的扇面运动脱钩。然而,始祖鸟的尾巴在几个重要方面与这种结构不同。始祖鸟可能具有有限的升力范围,并且椎骨运动和尾羽运动之间紧密耦合。这使得这种原始飞行者的尾巴更适合稳定而非机动。在鸟类进化过程中,能够显著改变升力并操纵飞行表面而不产生变形,可能是有利于尾巴缩短和尾综骨发育的两个因素。