The Grotte du Bison, in Arcy-sur-Cure (Yonne, France), yielded a large assemblage of 49 Neandertal remains from late Mousterian layers, offering critical insights for the study of Middle to Upper Paleolithic populations of Western Europe. Previous studies described the external morphology of 13 isolated teeth and a partial maxilla. Building on this previous work, the current study provides further descriptions and analyses of the remains, including one postcranial fragment, six cranial fragments, two maxillary fragments, and 40 isolated teeth. The dental remains are examined for a more detailed assessment of the metric and nonmetric variability of their external and internal morphology. We focus our description on preservation, health status, age at death and we assess the minimum number of individuals. The dental variability is also compared to that of Middle and Upper Pleistocene hominins. Our results indicate that the collection represents at least nine to 17 individuals, comprising mostly children and adolescents. Five to seven pairings are identified based on shared dental traits, developmental criteria, such as perikymata and pitted hypoplasia, wear patterns, and taphonomic alterations. This collection exhibit characteristic Neandertal features, including occasionally markedly expressed traits (e.g., I1 and P3 ridging and tubercular expressions), as well as a homogenous expression of accessory structures (particularly for the molars). The highest morphological variability is observed on maxillary premolar roots, which display different stages of root fusion, mesially placed hypercementosis, and pulp cavity extension. This collection also reflects the morphological and behavioral diversity observed in the other Arcy-sur-Cure caves.

Understanding the mechanism underlying the evolution of knuckle-walking in African great apes but not in humans may provide important implications about the origin and evolution of human bipedal locomotion. In this study, aiming to reveal possible structural adaptations of the chimpanzee's forearm and hand musculature related to knuckle-walking, we measure the passive elastic moment of the chimpanzee's and orangutan's wrist as it was rotated into extension, immobilizing the metacarpophalangeal joint at three different positions: extended (as in knuckle-walking), flexed (as in fist-walking), and an intermediate position. Our findings demonstrate that when the metacarpophalangeal joints are extended, the rigidity of the wrist joint in the extended direction increases. This increased rigidity is attributed to the passive elongation and force generation of digital flexor muscles, which are relatively short in chimpanzees. Consequently, this enhanced wrist-joint rigidity contributes to the stability and energetically efficient transmission of propulsive force to the ground during the stance phase. Overall, our study supports the hypothesis that knuckle-walking is an adaptation to terrestrial locomotion for an ancestor characterized by the restricted capacity for wrist extension owing to the relatively shorter tendons of digital flexor muscles.