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Chronic positive energy balance has surged among societies worldwide due to increasing dietary energy intake and decreasing physical activity, a phenomenon called the energy balance transition. Here, we investigate the effects of this transition on bone mass and strength. We focus on the Indigenous peoples of New Mexico in the United States, a rare case of a group for which data can be compared between individuals living before and after the start of the transition. We show that since the transition began, bone strength in the leg has markedly decreased, even though bone mass has apparently increased. Decreased bone strength, coupled with a high prevalence of obesity, has resulted in many people today having weaker bones that must sustain excessively heavy loads, potentially heightening their risk of a bone fracture. These findings may provide insight into more widespread upward trends in bone fragility and fracture risk among societies undergoing the energy balance transition.

 

Evidence for a reduction in stature between Mesolithic foragers and Neolithic farmers has been interpreted as reflective of declines in health, however, our current understanding of this trend fails to account for the complexity of cultural and dietary transitions or the possible causes of phenotypic change. The agricultural transition was extended in primary centers of domestication and abrupt in regions characterized by demic diffusion. In regions such as Northern Europe where foreign domesticates were difficult to establish, there is strong evidence for natural selection for lactase persistence in relation to dairying. We employ broad-scale analyses of diachronic variation in stature and body mass in the Levant, Europe, the Nile Valley, South Asia, and China, to test three hypotheses about the timing of subsistence shifts and human body size, that: 1) the adoption of agriculture led to a decrease in stature, 2) there were different trajectories in regions of in situ domestication or cultural diffusion of agriculture; and 3) increases in stature and body mass are observed in regions with evidence for selection for lactase persistence. Our results demonstrate that 1) decreases in stature preceded the origins of agriculture in some regions; 2) the Levant and China, regions of in situ domestication of species and an extended period of mixed foraging and agricultural subsistence, had stable stature and body mass over time; and 3) stature and body mass increases in Central and Northern Europe coincide with the timing of selective sweeps for lactase persistence, providing support for the “Lactase Growth Hypothesis.”

 

The foot plays a prominent role in weight-bearing suggesting it may reflect locomotor variation. Despite the immense amount of foot research, the calcaneus has been relatively understudied. Here we analyzed the entire calcaneal shape of Gorilla gorilla gorilla (n=41), Gorilla beringei graueri (n=17) and Gorilla beringei beringei (n=8) to understand how morphology relates to locomotor behavior. Calcanei were surface scanned and external shape analyzed using a three-dimensional geometric morphometric sliding semilandmark analysis. Semilandmarks were slid to minimize the bending energy of the thin plate spline interpolation function relative to the updated Procrustes average. Generalized Procrustes Analysis was used to align landmark configurations and shape variation was summarized using a principal components analysis. Procrustes distances between species were calculated and resampling statistics were run to test for group differences. All subspecies demonstrate statistically different morphologies (p<0.005 for pairwise comparisons). G. b. graueri separates from other subspecies based on posterolateral morphology, with G. b. graueri demonstrating an elongated peroneal trochlea, and thus more bone superiorly than G. g. gorilla. Compared to G. b. beringei, G. b. graueri has less bone inferiorly near the tuberosity. Cuboid and posterior talar facet shapes correlate with arboreality. G. b. beringei (most terrestrial) has a flatter cuboid facet and a more transversely oriented/relatively smaller posterior talar facet than G. g. gorilla (most arboreal) and G. b. graueri represents an intermediate morphology. These differences demonstrate a relationship between calcaneal shape and locomotor behavior and suggest that G. b. graueri may load its foot differently from the other subspecies. This project was supported by NSF grant # BCS - 1824630. 

Among human and nonhuman apes, calcaneal morphology exhibits significant variation that has been related to locomotor behavior. Due to its role in weight‐bearing, however, both body size and locomotion may impact calcaneal morphology. Determining how calcaneal morphologies vary as a function of body size is thus vital to understanding calcaneal functional adaptation. Here, we study calcaneus allometry and relative size in humans (n = 120) and nonhuman primates (n = 278), analyzing these relationships in light of known locomotor behaviors. Twelve linear measures and three articular facet surface areas were collected on calcaneus surface models. Body mass was estimated using femoral head superoinferior breadth. Relationships between calcaneal dimensions and estimated body mass were analyzed across the sample using phylogenetic least squares regression analyses (PGLS). Differences between humans and pooled nonhuman primates were tested using RMA ANCOVAs. Among (and within) genera residual differences from both PGLS regressions and isometry were analyzed using ANOVAs with post hoc multiple comparison tests. The relationships between all but two calcaneus dimensions and estimated body mass exhibit phylogenetic signal at the smallest taxonomic scale. This signal disappears when reanalyzed at the genus level. Calcaneal morphology varies relative to both body size and locomotor behavior. Humans have larger calcanei for estimated body mass relative to nonhuman primates as a potential adaptation for bipedalism. More terrestrial taxa exhibit longer calcaneal tubers for body mass, increasing the triceps surae lever arm. Among nonhuman great apes, more arboreal taxa have larger cuboid facet surface areas for body mass, increasing calcaneocuboid mobility.

 

While many attempts have been made to estimate body mass in hominins from lower limb bone dimensions, the upper limb has received far less attention in this regard. Here we develop new body mass estimation equations based on humeral articular breadths in a large modern human sample and apply them to 95 Plio‐Pleistocene specimens.

Humeral head superoinferior and total distal articular mediolateral breadths were measured in a morphologically diverse sample of 611 modern human skeletons whose body masses were estimated from bi‐iliac breadth and reconstructed stature. Reduced major axis regressions were used to compute body mass estimation equations. Consistency of the resulting estimates with those derived previously using lower limb bone equations was assessed in matched Plio‐Pleistocene individuals or samples.

In the modern reference sample, the new humeral body mass estimation equations exhibit only slightly lower precision compared to the previously derived lower limb bone equations. They give generally similar estimates for PleistoceneHomo, after accounting for the different shape of the humeral head articular surface in archaic Middle and Late PleistoceneHomo, except for distal humeral estimates for Late Pleistocene specimens, which average somewhat below lower limb estimates. Humeral equations give body mass estimates for australopiths that appear much too high, except forAustralopithecus sediba. A chimpanzee‐based distal humeral articular formula appears to work well for larger australopith specimens.

The new formulae provide a more secure foundation for estimating hominin body mass from humeri than previously available equations.

 

A number of studies have demonstrated the ontogenetic plasticity of long bone diaphyseal structure in response to mechanical loading. Captivity should affect mechanical loading of the limbs, but whether captive apes grow differently than wild apes has been debated. Here, we compare captive and wild juvenile and adultGorillato ascertain whether growth trajectories in cross‐sectional diaphyseal shape are similar in the two environments.

A sample of young juvenile (n = 4) and adult (n = 10) captiveGorilla gorillagorillaspecimens, with known life histories, were compared with age‐matched wildG.g. gorilla(n = 62) andG. beringei beringei(n = 75) in relative anteroposterior to mediolateral bending strength of the femur, tibia, and humerus. Cross sections were obtained using peripheral quantitative CT.

Captive and wild adultG.g. gorilladiffered in bending strength ratios for all three bones, but these differences were not present in young juvenileG.g. gorilla. In comparisons across taxa, captive juvenileG.g. gorillawere more similar to wildG.g. gorillathan toG.b. beringei, while captive adultG.g. gorillawere more similar in shape toG.b. beringeiin the hind limb.

Captive and wildG. gorillafollow different ontogenetic trajectories in long bone diaphyseal shape, corresponding to environmental differences and subsequent modified locomotor behaviors. Differences related to phylogeny are most evident early in development.