The small didelphid cmarsupial, Monodelphis domestica, uses a lateral sequence walk during slow treadmill locomotion and gradually shifts to a trot as speed increases. At higher speeds it changes abruptly to a half-bound. Cinematographic records suggest significant lateral bending but no sagittal bending of the trunk during the slow walk and a reduced amount of lateral bending during the fast walk. There is slight lteral, but no sagittal, bending during the trot. Sagittal bending is obvious during the half-bound, but no lateral bending is evident. Cineradiography confirms that the vertebral column of the trunk bends laterally during the slow walk. Bending occurs throughout the trunk region, but seems to be most pronounced in the anterior lumbar region. Associated with this bending of the trunk is substantial rotation of the pelvic girdle in the plane of yaw. Pelvic rotation is synchronized with the locomotor cycle of hindlimbs. Each side of the pelvis rotates forward during the recovery phase of the ipsilateral hindlimb and backward during the contact phase of this limb. Information on locomotor trunk movements in other limbed tetrapods is limited. The pattern of trunk bending found in Monodelphis, however, is consistent with that reported in the placental mammal Felis catus and in some lepidosaurian reptiles. This suggests that sagittal bending did not replace lateral bending during the evolution of mammals, as is sometimes suggested. Rather, bending in the vertical plane seems to have been added to lateral bleeding when the ancestors of extant mammals acquired galloping and bounding capabilities.
Recent claims that conodonts are members of the Craniata or Vertebrata are based in part upon soft tissue features that have been preserved in a small number of specimens. These features include what appear to be radials in the caudal fin and paired structures that have been identified as eye remnants. The evidence for radials is limited, but credible. However, the anatomy of extant cyclostomes suggests that the paired structures are more reasonably interpreted as otic capsules than the remnants of sclerotic eye capsules. Moreover, even if these structures are the remnants of eyes, conodonts might equally well be a sister group to the craniates as a member of that group. Aside from these paired structures, conodont fossils exhibit no features that are suggestive of a cartilaginous skeleton. Given that cyclostome fossils sometimes show evidence of the cartilages of the head, the apparent absence of a similar skeleton in conodont animals calls into question the claim that they are craniates. The simple single chevron shape of conodont myomeres also suggests that they lie outside of the Craniata. All living craniates have double‐chevron myomeres as adults, whereas simple myomeres of the conodont type are found in the non‐craniate cephalochordates. Thus the available soft tissue evidence suggests that conodonts are best regarded as the sister group of the craniates.
With 10 figures in the text) Cineradiographic analysis of the limb movements of Ornithorhynchus reveals that the proximal limb bones undergo horizontal retraction, long-axis rotation and distal elevation (humerus) or depression (femur) during the propulsive phase of walking. Cinematographic records show that the locomotor movements of Ornithorhynchus differ in several respects from those of Tuchyglossus and Zaglossus which are essentially similar. Comparison of the propulsive phase limb movements of Ornithorhynchus with those previously established radiographically for Tuchyglossus reveals that the humerus is on average less laterally but more dorsally directed, and that the femur is on average more dorsally and slightly more laterally directed in Ornithorhynchus. Comparison of the limb orientations of monotremes with those empirically determined in therian mammals and lepidosaurian reptiles indicates that monotremes are most similar to therians. Consideration of several evidently derived features of the appendicular skeleton of monotremes leads to the conclusion that the limb orientations used by early mammals were probably similar to those used by locomotively generalized living therians, and that monotremes show modifications of this.
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