2012
DOI: 10.1002/ajpa.22109
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Brief communication: Paleobiological inferences on the locomotor repertoire of extinct hominoids based on femoral neck cortical thickness: The fossil great ape hispanopithecus laietanus as a test‐case study

Abstract: The relationship between femoral neck superior and inferior cortical thickness in primates is related to locomotor behavior. This relationship has been employed to infer bipedalism in fossil hominins, although bipeds share the same pattern of generalized quadrupeds, where the superior cortex is thinner than the inferior one. In contrast, knuckle-walkers and specialized suspensory taxa display a more homogeneous distribution of cortical bone. These different patterns, probably related to the range of movement a… Show more

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Cited by 28 publications
(12 citation statements)
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References 27 publications
(96 reference statements)
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“…Rose stated: 'the fact of the ubiquity of quadrupedalism as a major locomotor mode in Miocene catarrhines in general, and Miocene hominoids in particular, is an inevitable starting point for any attempt to reach a full understanding of the emergence of the suspensory, quadrumanous climbing, quadrupedal-climbing-suspensory and bipedal specializations of extant hominoids' 54 . This agrees with claims that the mechanical requirements imposed by quadrupedalism and bipedalism are more similar to each other than to those related to suspension 37,55 . Our results therefore support a modified version of the evolutionary scenario that early bipeds might have evolved from a more generalized arboreal, largely orthograde (but not specifically suspensory) Miocene ape 11,14,15,25,45 , with a more plesiomorphic postcranium than that exhibited by any of the extant African apes 8,16 .…”
Section: Discussionsupporting
confidence: 90%
See 1 more Smart Citation
“…Rose stated: 'the fact of the ubiquity of quadrupedalism as a major locomotor mode in Miocene catarrhines in general, and Miocene hominoids in particular, is an inevitable starting point for any attempt to reach a full understanding of the emergence of the suspensory, quadrumanous climbing, quadrupedal-climbing-suspensory and bipedal specializations of extant hominoids' 54 . This agrees with claims that the mechanical requirements imposed by quadrupedalism and bipedalism are more similar to each other than to those related to suspension 37,55 . Our results therefore support a modified version of the evolutionary scenario that early bipeds might have evolved from a more generalized arboreal, largely orthograde (but not specifically suspensory) Miocene ape 11,14,15,25,45 , with a more plesiomorphic postcranium than that exhibited by any of the extant African apes 8,16 .…”
Section: Discussionsupporting
confidence: 90%
“…If this is indeed the case, our results indicate an adaptive shift towards enhanced mobility at the hip joint in hominoids relative to non-hominoid anthropoids that was already present by the early Miocene (as evidenced by Proconsul). These results expand previous analyses indicating significantly larger heads relative to neck in great apes as compared with Macaca 31 , as well as inferences derived from femoral morphology in Miocene hominoids 19,[36][37][38][39] . Conversely, the primitive pelvis of Proconsul 19 suggests mosaic evolution across both sides of the hominoid hip joint.…”
Section: Discussionsupporting
confidence: 88%
“…However, the evidence provided by Pierolapithecus [1], [2], [4], [8], [13] suggests that the acquisition of suspensory adaptations might have been decoupled from that of vertical climbing (contra [11], [14], [15])—with clear suspensory adaptations not being displayed until the late Miocene by Hispanopithecus / Rudapithecus (see discussion in [59], but also [13][15], [17], [52], [60][62]). Concerning the latter taxa, the below-branch suspensory adaptations observed on their femora [52], [60], [61], [63], [64] and other postcranial remains [13][15], [17], [60][62] lead us to predict, based on our analyses above, that the patella of Hispanopithecus (if ever found) would probably resemble those of modern great apes, like in Pierolapithecus and Oreopithecus .…”
Section: Discussionmentioning
confidence: 68%
“…Main references: Villalta Comella and Crusafont Pairó (1944) ;Crusafont Pairó (1958b, 1965a; Hürzeler (1961, 1969); Crusafont-Pairó and GolpePosse (1973a);Golpe Posse (1982a; Moyà ; Begun et al (1990); Harrison (1991); Moyà- Solà and Köhler (1993a, 1995; Andrews et al (1996);Cameron (1997Cameron ( , 1999; Köhler et al ( , 2001aKöhler et al ( , b, 2002; Ribot et al (1996);Begun (2002bBegun ( , 2009Checa Soler and Rius Font (2003); Almécija et al (2007); ; Alba et al (2010aAlba et al ( , c, 2011bAlba et al ( , 2012b); Casanovas-Vilar et al (2011);Susanna et al (2011);Pickford (2012); Pina et al (2012b); Alba (2012). (Begun, 1992) ( Fig.…”
Section: Subfamily Homininae Gray 1825mentioning
confidence: 99%