Hominoids and atelines are known to use suspensory behaviors and are assumed to possess greater hip joint mobility than non-suspensory monkeys, particularly for range of abduction. This assumption has greatly influenced how extant and fossil primate hip joint morphology has been interpreted, despite the fact that there are no data available on hip mobility in hominoids or Ateles. This study uses in vivo measurements to test the hypothesis that suspensory anthropoids have significantly greater ranges of hip joint mobility than non-suspensory anthropoids. Passive hip joint mobility was measured on a large sample of anesthetized captive anthropoids (non-human hominids=43, hylobatids=6, cercopithecids=43, Ateles=6, Cebus=6). Angular and linear data were collected using goniometers and tape measures. Range of motion data were analyzed for significant differences by locomotor group using ANOVA and phylogenetic regression. The data demonstrate that suspensory anthropoids are capable of significantly greater hip abduction and external rotation. Degree of flexion and internal rotation were not larger in the suspensory primates, indicating that suspension is not associated with a global increase in hip mobility. Future work should consider the role of external rotation in abduction ability, how the physical position of the distal limb segments are influenced by differences in range of motion proximally, as well as focus on bony and soft tissue differences that enable or restrict abduction and external rotation at the anthropoid hip joint.
Humans diverged from apes (chimpanzees, specifically) toward the end of the Miocene ~9.3 million to 6.5 million years ago. Understanding the origins of the human lineage (hominins) requires reconstructing the morphology, behavior, and environment of the chimpanzee-human last common ancestor. Modern hominoids (that is, humans and apes) share multiple features (for example, an orthograde body plan facilitating upright positional behaviors). However, the fossil record indicates that living hominoids constitute narrow representatives of an ancient radiation of more widely distributed, diverse species, none of which exhibit the entire suite of locomotor adaptations present in the extant relatives. Hence, some modern ape similarities might have evolved in parallel in response to similar selection pressures. Current evidence suggests that hominins originated in Africa from Miocene ape ancestors unlike any living species.
Hip joint diameter is highly correlated with body size in primates and so can potentially provide important information about the biology of fossil hominins. However, quantifying hip joint size has been difficult or impossible for many important but fragmentary specimens. New three-dimensional technologies can be used to digitally fit spheres to the acetabular lunate surface, potentially allowing hip joint diameter estimates for incomplete joint surfaces. Here we evaluate the reliability of sphere-fitting to incomplete lunate surfaces in silico using three-dimensional polygonal models of extant anthropoid hipbones. Measurement error in lunate sphere-fitting was assessed at the individual observer level, as well as between observers. Prediction error was also established for acetabular sphere size estimates for smaller divisions of the lunate surface. Sphere-fitting techniques were then applied to undistorted regions of lunate surface in Plio-Pleistocene hominin pelves, with a range of diameters constructed from extant error estimates. The results of this study indicate that digital sphere-fitting techniques are precise and that the lunate does not need to be completely preserved to accurately infer hip dimensions, although some aspects of joint size and morphology can influence sphere size estimates. Joint diameter is strongly predicted by spheres fit to the cranial and caudal halves of the lunate in all anthropoids. We present new hip joint size estimates for a number of fossil hominins, and outline additional applications for digital sphere-fitting as a morphometric technique.
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