Abstract:In spite of its importance for movements of the upper limbs, the clavicle is an infrequently studied shoulder bone. The present study compares clavicular morphology among different extant primates. Methods have included the assessment of clavicular curvatures projected on two perpendicular planes that can be assessed overall as cranial and dorsal primary curvatures. Results showed that in cranial view, three morphologies can be defined. One group exhibited an external curvature considerably more pronounced tha… Show more
“…333x-6/9 is distinct from other hominoids in the orientation of its lateral end (on frontal view) and in the position of the deltoid attachment area, features which he interpreted as evidence of descent of the hominin shoulder by three to four million years ago. However, in his analysis of clavicular shape in primates, Voisin 16 reports that the uniquely low shoulder position in humans is indicated, on dorsal view, by a distinctive curvature of the medial rather than the lateral end of the human clavicle. Although A.L.…”
“…333x-6/9 is distinct from other hominoids in the orientation of its lateral end (on frontal view) and in the position of the deltoid attachment area, features which he interpreted as evidence of descent of the hominin shoulder by three to four million years ago. However, in his analysis of clavicular shape in primates, Voisin 16 reports that the uniquely low shoulder position in humans is indicated, on dorsal view, by a distinctive curvature of the medial rather than the lateral end of the human clavicle. Although A.L.…”
“…Understanding the evolutionary process of these features is pivotal for the study of living hominoid evolution. Numerous studies have examined hominoid skeletal morphology in the forelimb, shoulder girdle and vertebral column (Cartmill and Milton 1977;Larson 1988Larson , 1998Rose 1988Rose , 1989Takahashi 1990;Gebo 1993Gebo , 1996Ward 1993;Voisin 2006). However, comparatively fewer morphological studies have been undertaken on the living (Schultz 1956(Schultz , 1961Erikson 1963;Ohman 1986;Gebo 1996;Chan 1997;Preuschoft et al 2003) and fossil (Schultz 1960;Schmid 1983Schmid , 1991Jellema et al 1993;Moyà-Solà et al 2004;Sawyer and Maley 2005) hominoid thoracic region.…”
While a relatively broad thorax and strongly curved ribs are widely regarded as common features of living hominoids, few studies have quantitatively examined these traits by methods other than calculating the chest index. The present study aims to quantify variations in thoracic cage morphology for living anthropoids. The odd-numbered ribs (first to eleventh) were articulated with the corresponding vertebrae and the cranial and lateral views subsequently photographed. Rib profiles were digitized in both views and line-fitted by a Bézier curve to create a three-dimensional morphological data set. When thoracic cage width was scaled against body mass, Hylobates (and possibly Pongo) plotted above non-hominoid anthropoids at almost all rib levels, while Pan did not differ from non-hominoid anthropoids. The overall pattern of the normalized thoracic width differed between Hylobates and other hominoids. In Hylobates, an upward convex curve was seen between the first and seventh ribs while a more linear pattern was observed in Pan and Pongo. This result quantitatively confirmed that the barrel-shaped thoracic cage in Hylobates can be distinguished from the funnel-shaped form in other hominoids. Conversely, all hominoids shared two distinct features in the upper half-thorax: (1) a pronounced dorsal protrusion of the proximal part of the rib in accordance with ventral displacement of the thoracic spine and (2) a relatively medially projecting sternal end. Although these features are likely to provide some mechanical advantage in orthograde and/or suspensory positional behaviors, they were barely present in the suspensory Ateles.
“…One essential, and unique, feature, compared to other laboratory animals, was the presence of a clavicle that enabled movements of the upper limb similar to humans. 24 Furthermore, the pectoral implantation site of the IPM in the baboons compared very well with those of humans. The material density of the Pectoralis major muscle of 1.115 ± 0.055 g/cm 3 of this study, determined on freshly excised tissue, compared well with previously reported values for mammalian muscle tissue of 1.112 ± 0.006 g/cm 3 , measured on muscle tissue after fixation in 4% formaldehyde.…”
Recently we presented a method for the assessment of in vivo forces on pectoral device implants motivated from technological and clinical advancements toward smaller implantable cardiac pacemakers and the altered structural demands arising from the reduced device size. Objective of this study was the investigation of the intra-species proportionality of in-line force and transverse reaction force of the Pectoralis major for the characterization of mechanical in vivo loadings on pectoral implants. Two Chacma baboons (23.9 ± 1.2 kg) received bilaterally one chronic and one acute pectoral sub-muscular instrumented pacemaker (IPM) implant. The Pectoralis major muscle was electrically stimulated and resulting in-line and transverse muscle force were measured. The correlation of in-line force and transverse force of the Pectoralis major was investigated using linear regression analyses. The proportionality of in-line and transverse force of the Pectoralis major was found to be subject-specific (R² = 0.17, p < 0.003). Including morphometric parameters, i.e., length along line of action, width over implant and stress, in the regression analysis provided a strong intra-species correlation between in-line and transverse force (R² = 0.71, p < 10⁻⁷). The novel intra-species correlation provides a tool toward the characterization of mechanical in vivo loading conditions of pectoral device implants.
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