2016
DOI: 10.1002/ajpa.22930
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Long bone cross‐sectional properties reflect changes in locomotor behavior in developing chimpanzees

Abstract: Taken together, these findings contribute to our understanding of how ontogenetic changes in function affect form. As similar changes may have characterized the behavioral and skeletal ontogeny of extinct hominoids including hominins, these findings furnish a potential means to make inferences about the behavior of fossil taxa based on the structural properties of their bones.

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Cited by 62 publications
(84 citation statements)
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References 66 publications
(148 reference statements)
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“…Among great apes, forelimb to hind limb strength proportions parallel the degree of arboreality, from orangutans to chimpanzees to Western lowland gorillas to mountain gorillas, the most terrestrial nonhuman hominoid [43, 94]. Furthermore, within both mountain gorillas and common chimpanzees, ontogenetic declines in arboreal locomotion are associated with declines in forelimb to hind limb strength [31, 32]. It should be noted that these trends are not simply a function of differences or changes in overall limb bone size, e.g., length, as lowland and mountain gorillas have similar limb length proportions but different strength proportions, and ontogenetic changes in limb length proportions in mountain gorillas do not parallel those in strength proportions [31].…”
Section: Discussionmentioning
confidence: 99%
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“…Among great apes, forelimb to hind limb strength proportions parallel the degree of arboreality, from orangutans to chimpanzees to Western lowland gorillas to mountain gorillas, the most terrestrial nonhuman hominoid [43, 94]. Furthermore, within both mountain gorillas and common chimpanzees, ontogenetic declines in arboreal locomotion are associated with declines in forelimb to hind limb strength [31, 32]. It should be noted that these trends are not simply a function of differences or changes in overall limb bone size, e.g., length, as lowland and mountain gorillas have similar limb length proportions but different strength proportions, and ontogenetic changes in limb length proportions in mountain gorillas do not parallel those in strength proportions [31].…”
Section: Discussionmentioning
confidence: 99%
“…One such trait is the cross-sectional structure of long bone diaphyses, which is known from both experimental and observational studies to be responsive to changes in mechanical loadings during life [2729]. Thus, for example, changes in inter-limb bone diaphyseal strength proportions accurately reflect changes in locomotor behavior during development in humans, gorillas, and chimpanzees [3032]. Limb bone strength proportions in early Homo erectus (KNM-ER 1808 and KNM-WT 15000) are similar to those in modern humans [33], supporting other evidence for completely modern terrestrial locomotor behavior in this taxon [34].…”
Section: Introductionmentioning
confidence: 99%
“…This is of particular relevance for African apes, as the percentage of knuckle‐walking and suspension change significantly during development (Doran, , ; Sarringhaus et al. , ), although long bone cross‐sectional geometry in African apes continues to change into adulthood and reflect locomotor behaviour at different life stages (Ruff et al. ; Sarringhaus et al.…”
Section: Introductionmentioning
confidence: 99%
“…As the rate of remodelling of bone is higher during growth, behaviours during development may be more important for explaining trabecular morphology than those during adulthood (Bertram & Swartz, 1991;Pettersson et al 2010). This is of particular relevance for African apes, as the percentage of knuckle-walking and suspension change significantly during development (Doran, 1992(Doran, , 1997Sarringhaus et al 2014Sarringhaus et al , 2016, although long bone cross-sectional geometry in African apes continues to change into adulthood and reflect locomotor behaviour at different life stages (Ruff et al 2013;Sarringhaus et al 2016; but see Demes et al 1998Demes et al , 2001Lieberman et al 2004;Carlson, 2005). Trabecular morphology may differ due to anatomical location (Morgan & Keaveny, 2001;Eckstein et al 2007;Wallace et al 2015); for example, distal limb elements may be adapted to have a lower bone mass (bone mineral density measured using pQCT and multiplied by joint size) and BV/TV than more proximal limb elements (Chirchir, 2015;Saers et al 2016).…”
Section: Introductionmentioning
confidence: 99%
“…For the purposes of analyzing developmental change, infant chimpanzees were categorized into 4 age groups, based on those used in the previous literature, and consistent with locomotor development [e.g., Plooij, 1984;Hiraiwa-Hasegawa, 1989;Sarringhaus et al, 2016;Matsumoto, 2017]: < 7 months, 8-18 months, 19-36 months, and 37-69 months. Note that 25 of 37 dyads contributed more than one data point.…”
Section: Methodsmentioning
confidence: 99%