Zippel Kevin C, Glor Richard E, Bertram John E A
Section of Ecology and Systematics, Cornell University, Ithaca, New York 14853.
Department of Anatomy, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853.
J Morphol. 1999 Feb;239(2):143-155. doi: 10.1002/(SICI)1097-4687(199902)239:2<143::AID-JMOR3>3.0.CO;2-O.
We examined caudal anatomy in two species of prehensile-tailed lizards, Furcifer pardalis and Corucia zebrata. Although both species use their tails to grasp, each relies on a strikingly different anatomy to do so. The underlying anatomies appear to reflect phylogenetic constraints on the consequent functional mechanisms. Caudal autotomy is presumably the ancestral condition for lizards and is allowed by a complex system of interdigitating muscle segments. The immediate ancestor of chameleons was nonautotomous and did not possess this specialized anatomy; consequently, the derived arrangement in the chameleon tail is unique among lizards. The limb functions as an articulated linkage system with long tendinous bands originating from longitudinal muscles to directly manipulate vertebrae. Corucia is incapable of autotomy, but it is immediately derived from autotomous ancestors. As such, it has evolved a biomechanical system for prehension quite different from that of chameleons. The caudal anatomy in Corucia is very similar to that of lizards with autotomous tails, yet distinct differences in the ancestral pattern and its relationship to the subdermal tunic are derived. Instead of the functional unit being individual autotomy segments, the interdigitating prongs of muscle have become fused with an emphasis on longitudinal stacks of muscular cones. The muscles originate from the vertebral column and a subdermal collagenous tunic and insert within the adjacent cone. However, there is remarkably little direct connection with the bones. The muscles have origins more associated with the tunic and muscular septa. Like the axial musculature of some fish, the tail of Corucia utilizes a design in which these collagenous elements serve as an integral skeletal component. This arrangement provides Corucia with an elegantly designed system capable of a remarkable variety of bending movements not evident in chameleon tails. J. Morphol. 239:143-155, 1999. © 1999 Wiley-Liss, Inc.
我们研究了两种卷尾蜥蜴,豹纹变色龙(Furcifer pardalis)和绿安乐蜥(Corucia zebrata)的尾部解剖结构。尽管这两个物种都用尾巴抓握物体,但它们实现抓握所依赖的解剖结构却截然不同。其潜在的解剖结构似乎反映了系统发育对后续功能机制的限制。尾自割现象大概是蜥蜴的原始状态,它由一个复杂的相互交错的肌肉节段系统所促成。变色龙的直系祖先不会自割尾巴,也不具备这种特殊的解剖结构;因此,变色龙尾巴的衍生结构在蜥蜴中是独一无二的。其肢体起到一个关节连接系统的作用,长腱带起源于纵向肌肉,可直接操纵椎骨。绿安乐蜥无法自割尾巴,但它直接起源于能够自割尾巴的祖先。因此,它进化出了一种与变色龙截然不同的抓握生物力学系统。绿安乐蜥的尾部解剖结构与具有自割尾巴的蜥蜴非常相似,但在原始模式及其与皮下被膜的关系上存在明显差异。肌肉的相互交错的叉状结构没有成为独立的自割节段,而是融合在一起,形成了以纵向排列的肌肉锥体为主的结构。肌肉起源于脊柱和皮下胶原被膜,并插入相邻的锥体中。然而,与骨骼的直接连接非常少。肌肉的起源更多地与被膜和肌肉隔膜相关。就像一些鱼类的轴向肌肉组织一样,绿安乐蜥的尾巴采用了一种设计,其中这些胶原成分作为一个不可或缺的骨骼组成部分。这种结构为绿安乐蜥提供了一个设计精巧的系统,能够进行各种变色龙尾巴所不具备的弯曲运动。《形态学杂志》239:143 - 155,1999年。© 1999威利 - 利斯公司。