Bipedalism is a key adaptation that differentiates hominins (humans and our extinct relatives) from living and fossil apes. The earliest putative hominin, Sahelanthropus tchadensis (~7 million years old), was originally represented by a cranium, the reconstruction of which suggested to its discoverers that Sahelanthropus carried its head in a manner similar to known bipedal hominins. Recently, two partial ulnae and a femur shaft were announced as evidence in support of the contention that Sahelanthropus was an early biped, but those interpretations have been challenged. Here, while we find that both limb bones are most similar in size and geometric morphometric shape to chimpanzees (genus Pan), we demonstrate that their relative proportion is more hominin-like. Furthermore, we confirm two features linked to hominin-like hip and knee function and identify a femoral tubercle, a feature only found in bipedal hominins. Our results suggest that Sahelanthropus was an early biped that evolved from a Pan-like Miocene ape ancestor.

Because the ulna supports and transmits forces during movement, its morphology can signal aspects of functional adaptation. To test whether, like extant apes, some hominins habitually recruit the forelimb in locomotion, we separate the ulna shaft and ulna proximal complex for independent shape analyses via elliptical Fourier methods to identify functional signals. We examine the relative influence of locomotion, taxonomy, and body mass on ulna contours in Homo sapiens (n = 22), five species of extant apes (n = 33), two Miocene apes (Hispanopithecus and Danuvius), and 17 fossil hominin specimens including Sahelanthropus, Ardipithecus, Australopithecus, Paranthropus, and early Homo. Ulna proximal complex contours correlate with body mass but not locomotor patterns, while ulna shafts significantly correlate with locomotion. African apes' ulna shafts are more robust and curved than Asian apes and are unlike other terrestrial mammals (including other primates), curving ventrally rather than dorsally. Because this distinctive curvature is absent in orangutans and hylobatids, it is likely a function of powerful flexors engaged in wrist and hand stabilization during knuckle-walking, and not an adaptation to climbing or suspensory behavior. The OH 36 (purported Paranthropus boisei) and TM 266 (assigned to Sahelanthropus tchadensis) fossils differ from other hominins by falling within the knuckle-walking morphospace, and thus appear to show forelimb morphology consistent with terrestrial locomotion. Discriminant function analysis classifies both OH 36 and TM 266 with Pan and Gorilla with high posterior probability. Along with its associated femur, the TM 266 ulna shaft contours and its deep, keeled trochlear notch comprise a suite of traits signaling African ape-like quadrupedalism. While implications for the phylogenetic position and hominin status of S. tchadensis remain equivocal, this study supports the growing body of evidence indicating that S. tchadensis was not an obligate biped, but instead represents a late Miocene hominid with knuckle-walking adaptations.

In their recent article, “The atlas of StW 573 and the late emergence of human-like head mobility and brain metabolism” Beaudet and colleagues (Scientific Reports, March 2020) contend that StW 573 had lower metabolic costs for cerebral tissues and that blood perfusion of these tissues increased recently over the course of hominin evolution. This conclusion is in large part based on the assumption of a correlation between the size of the fossil vertebra’s transverse foramen and arterial canal diameters, and by extension, they use the foramen’s cross-sectional area in conjunction with the size of the cranium’s carotid canal to reconstruct blood flow volume to the brain as a proxy of the brain’s metabolic demands. As I show here, these assumptions are unsupported because the C1 cervical vertebra cannot help indicate hemodynamics or investment in brain metabolism.

Archaeological excavations at the Dali site complex located in southeastern Kazakhstan provide a rich picture of Bronze Age life spanning from the early third to late second millennia B.C. Nearly ten years of research at the site have produced an abundant assemblage of architectural remains, ritual and burial contexts, human and animal ancient DNA, and evidence for related economic practices and other material forms (ceramics, metallurgy). A systematic radiocarbon dating program provides detailed chronological context for the numerous stratigraphically documented phases of occupation, burial, and economy at the site. The settlement contexts at Dali provide some of the most varied and well- dated material assemblages known in the region and help illustrate how local pastoralist societies developed traditions of architecture, ceramic production, herd management, and ritual in the Early Bronze Age, while innovating and incorporating novel craft techniques, economic strategies, burial styles, and settlement construction in the Middle and Late Bronze Age. Taken together, the archaeological data from Dali allow for a detailed reconstruction of the local practices and regional interactions that engaged agro-pastoralist communities within diverse, shared institutional domains across the Inner Asian Mountain Corridor and beyond over a span of more than 2000 years.

Objectives In humans and known fossil hominins, lumbar lordosis is produced by vertebral body wedging and other bony and soft tissue features such as the shape of the intervertebral discs. Current techniques for quantifying the wedging of vertebral bodies are limited in utility, especially when analyzing incomplete fossil material. Here, we introduce a 3D method to quantify vertebral body wedging angles that yields the angles between two “best fit” planes in the software GeoMagic Wrap (3D Systems). Materials and Methods To test that this new method is repeatable with existing methods, we measure the wedging of 320 lumbar vertebrae representing 64 modern human individuals. For each vertebra, wedging angles were calculated from linear measurements taken with calipers and compared with estimates generated from the 3D best fit plane method. We also apply the 3D plane method to fossil hominin lumbar vertebrae, including newly described lumbar vertebrae of Homo naledi , the majority of which do not preserve the four landmarks necessary to calculate wedging angles using the traditional approach. Results The results of the two methods are highly and significantly correlated ( r 2 = 0.98, p < 0.0001). The 3D plane method was successfully applied to nearly all of the fossil hominin specimens included in the study. Discussion The new 3D plane method introduced here is repeatable with the traditional linear measurement method and allows for the estimation of wedging angles in incomplete material. When applied to Homo naledi lumbar vertebrae, similarities to other fossil hominins and modern humans are found.

Lumbar lordosis is a key adaptation to bipedal locomotion in the human lineage. Dorsoventral spinal curvatures enable the body's center of mass to be positioned above the hip, knee, and ankle joints, and minimize the muscular effort required for postural control and locomotion. Previous studies have suggested that Neandertals had less lordotic (ventrally convex) lumbar columns than modern humans, which contributed to historical perceptions of postural and locomotor differences between the two groups. Quantifying lower back curvature in extinct hominins is entirely reliant upon bony correlates of overall lordosis, since the latter is significantly influenced by soft tissue structures (e.g. intervertebral discs). Here, we investigate sexual dimorphism, ancestry, and lifestyle effects on lumbar vertebral body wedging and inferior articular facet angulation, two features previously shown to be significantly correlated with overall lordosis in living individuals, in a large sample of modern humans and Neandertals. Our results demonstrate significant differences between postindustrial cadaveric remains and archaeological samples of people that lived preindustrial lifestyles. We suggest these differences are related to activity and other aspects of lifestyle rather than innate population (ancestry) differences. Neandertal bony correlates of lumbar lordosis are significantly different from all human samples except preindustrial males. Therefore, although Neandertals demonstrate more bony kyphotic wedging than most modern humans, we cast doubt on proposed locomotor and postural differences between the two lineages based on inferred lumbar lordosis (or lack thereof), and we recommend future research compare fossils to modern humans from varied populations and not just recent, postindustrial samples.

AbstractAdaptations of the lower back to bipedalism are frequently discussed but infrequently demonstrated in early fossil hominins. Newly discovered lumbar vertebrae contribute to a near-complete lower back of Malapa Hominin 2 (MH2), offering additional insights into posture and locomotion inAustralopithecus sediba. We show that MH2 demonstrates a lower back consistent with human-like lumbar lordosis and other adaptations to bipedalism, including an increase in the width of intervertebral articular facets from the upper to lower lumbar column (“pyramidal configuration”). This contrasts with recent work on lordosis in fossil hominins, where MH2 was argued to demonstrate no appreciable lordosis (“hypolordosis”) similar to Neandertals. Our three-dimensional geometric morphometric (3D GM) analyses show that MH2’s nearly complete middle lumbar vertebra is human-like in shape but bears large, cranially-directed transverse processes, implying powerful trunk musculature. We interpret this combination of features to indicate thatA. sedibaused its lower back in both human-like bipedalism and ape-like arboreal positional behaviors, as previously suggested based on multiple lines of evidence from other parts of the skeleton and reconstructed paleobiology ofA. sediba.

Adaptations of the lower back to bipedalism are frequently discussed but infrequently demonstrated in early fossil hominins. Newly discovered lumbar vertebrae contribute to a near-complete lower back of Malapa Hominin 2 (MH2), offering additional insights into posture and locomotion in Australopithecus sediba . We show that MH2 possessed a lower back consistent with lumbar lordosis and other adaptations to bipedalism, including an increase in the width of intervertebral articular facets from the upper to lower lumbar column (‘pyramidal configuration’). These results contrast with some recent work on lordosis in fossil hominins, where MH2 was argued to demonstrate no appreciable lordosis (‘hypolordosis’) similar to Neandertals. Our three-dimensional geometric morphometric (3D GM) analyses show that MH2’s nearly complete middle lumbar vertebra is human-like in overall shape but its vertebral body is somewhat intermediate in shape between modern humans and great apes. Additionally, it bears long, cranially and ventrally oriented costal (transverse) processes, implying powerful trunk musculature. We interpret this combination of features to indicate that A. sediba used its lower back in both bipedal and arboreal positional behaviors, as previously suggested based on multiple lines of evidence from other parts of the skeleton and reconstructed paleobiology of A. sediba .

Sexual dimorphism is an important feature of adult thorax morphology, but when and how sex-related differences in the ribcage arise during ontogeny is poorly known. Previous research proposed that sex-related size differences in the nasal region arise during puberty. Therefore, we explore whether ribcage sexual dimorphism also arises at that time and whether this sexual dimorphism is maintained until old age. We measured 526 (semi)landmarks on 80 CT-based human ribcage reconstructions, on individuals ranging from 7 to 65 year-old. The 3D coordinates were submitted to the Procrustes superimposition and analyzed. Our results show that the trajectories of thorax size and shape between sexes diverge at around 12 years of age, and continue slightly diverging until old age. The differential ontogenetic trends cause adult male ribcages to become deeper, shorter, and wider than female. Our results are consistent with the evidence from the cranial respiratory system, with the development of sexual dimorphism probably related to changes in body composition during puberty combined with changes in the reproductive system.