Ecogeographic patterns in fetal limb proportions

2019 ◽  
Vol 169 (1) ◽  
pp. 93-103
Author(s):  
Erin B. Waxenbaum ◽  
Michael W. Warren ◽  
Trenton W. Holliday ◽  
John E. Byrd ◽  
Theodore M. Cole
Keyword(s):  
Paleobiology ◽  
1982 ◽  
Vol 8 (1) ◽  
pp. 16-30 ◽  
Author(s):  
Donald R. Prothero ◽  
Paul C. Sereno

Barstovian (medial Miocene) mammalian faunas from the Texas Gulf Coastal Plain contained four apparently sympatric species of rhinoceroses: the common forms Aphelops megalodus and Teleoceras medicornutus, a dwarf Teleoceras, and a dwarf Peraceras. Previous work has suggested positive allometry in tooth area with respect to body size in several groups of mammals, i.e., larger mammals have relatively more tooth area. However, dwarfing lineages were shown to have relatively more tooth area for their body size. Our data show no significant allometry in post-canine tooth area of either artiodactyls or ceratomorphs. Similarly, dwarf rhinoceroses and hippopotami show no more tooth area than would be predicted for their size. Limbs are proportionately longer and more robust in larger living ceratomorphs (rhinos and tapirs) than predicted by previous authors. Limb proportions of both dwarf rhinoceroses and dwarf hippopotami are even more robust than in their living relatives.The high rhinoceros diversity reflects the overall high diversity of Barstovian faunas from the Texas Gulf Coastal Plain. The first appearance of several High Plains mammals in these faunas indicates “ecotone”-like conditions as faunal composition changed. Study of living continental dwarfs shows that there is commonly an ecological separation between browsing forest dwarfs and their larger forebears, which are frequently savannah grazers. This suggests that the dwarf rhinoceroses might have been forest browsers which were sympatric with the larger grazing rhinos of the High Plains during the Barstovian invasion. The continental dwarf model also suggests that insular dwarfism may be explained by the browsing food resources that predominate on islands.


2011 ◽  
pp. 235-254 ◽  
Author(s):  
Luis Azevedo Rodrigues ◽  
Josep Daunis-i-Estadella ◽  
Glòria Mateu-Figueras ◽  
Santiago Thió-Henestrosa
Keyword(s):  

Author(s):  
Adam D. Gordon ◽  
David J. Green ◽  
William L. Jungers ◽  
Brian G. Richmond

Major changes in body shape occurred during human evolution, but questions remain about body shape in australopiths. The present study investigates the specifics of the presumed relationships between limb indices and positional behavior underlying prior work that compared proportions among extant hominids in order to make inferences about extinct hominins. We find that although both intermembral index or ratio of diaphyseal and articular proportions distinguish humans from great apes, neigher correlates well with variation in the degree of arboreality in the locomotor repertoire of extant hominids. Brachial index and a ratio of diaphyseal and articular dimensions from the fore- and hindlimb, however, do correlate with degree of arboreality, and scale slightly positively allometrically within species in all extant taxa. These two observations are taken into consideration in a more nuanced interpretation of a reanalysis of articular-diaphyseal limb proportions in an expanded sample of the Sterkfontein postcrania. This study confirms previous findings that Australopithecus africanus had larger forelimb dimensions in relation to hindlimb dimensions than modern humans and A. afarensis, similar to the patterns seen in extant apes, particularly western gorillas. However, data presented here suggest that interpreting a particular taxon as “human-like” or “ape-like” may be overly simplistic. Instead, while both A. africanus and A. afarensis were almost certainly committed bipeds that incorporated some arboreality into their locomotor repertoire, A. africanus apparently used a set of locomotor behaviors that was more distinct from that of A. afarensis than Pan troglodytes and Gorilla gorilla are from each other.


Author(s):  
Erik Trinkaus ◽  
Alexandra P. Buzhilova ◽  
Maria B. Mednikova ◽  
Maria V. Dobrovolskaya

The three partial skeletons from Sunghir retain substantial portions of their shoulder and arm remains, from the proximal clavicle to the distal radius and ulna. The scapulae, as with most of those from the Pleistocene, retain principally the spine, the glenoid area, the coracoid process, and the axillary border. The left forearm of Sunghir 2 is absent (as is his left hand), and the left humerus consists of a diaphyseal section without the metaphyses and a partial proximal epiphysis. It is nonetheless possible to assess both overall upper limb proportions (chapter 11) and a number of aspects that relate to upper limb asymmetry, clavicle and scapular morphology, glenohumeral proportions, diaphyseal robustness, cubital articulations, and reflections of pronation-supination hypertrophy for all three of them. Although humans are considered to be bilaterally symmetrical in their limbs, there are small degrees of asymmetry in most limb bones. These asymmetries are frequently exaggerated in the human upper limb, given our handedness and the subsequent preference for use of the dominant arm in more mechanically demanding activities (Raymond and Pontier 2004). In general, the level of asymmetry in the dimensions of epiphyses, and especially of articulations, is modest. However, substantial asymmetry in measures of upper limb diaphyses (particularly of the humerus) have been documented in samples of recent humans (e.g., Ruff and Jones 1981; Fresia et al. 1990; Trinkaus et al. 1994; Roy et al. 1994; Churchill 1994; Steele and Mays 1995; Sakaue 1997; Mays 2002; Auerbach and Ruff 2006; Cowgill 2008; Auerbach and Raxter 2008), as well as in a number of Late Pleistocene humans (e.g., Trinkaus et al. 1994; Churchill and Formicola 1997; Cowgill 2008; Shang and Trinkaus 2010; Cowgill et al. 2012b; Mednikova 2012; Volpato et al. 2012). Moreover, as is indicated by labial anterior dental striations and one individual’s forearm bones, such handedness extends back through the genus Homo (Weaver et al. 2001; Frayer et al. 2012).


PLoS ONE ◽  
2012 ◽  
Vol 7 (12) ◽  
pp. e51795 ◽  
Author(s):  
Emma Pomeroy ◽  
Jay T. Stock ◽  
Sanja Stanojevic ◽  
J. Jaime Miranda ◽  
Tim J. Cole ◽  
...  

2018 ◽  
Author(s):  
Jason L. Heaton ◽  
Travis Rayne Pickering ◽  
Kristian J. Carlson ◽  
Robin H. Crompton ◽  
Tea Jashashvili ◽  
...  

Due to its completeness, the A.L. 288-1 (Lucy) skeleton has long served as the archetypal bipedal Australopithecus. However, there remains considerable debate about its limb proportions. There are three competing, but not necessarily mutually exclusive, explanations for the high humerofemoral index of A.L. 288-1: (1) a retention of proportions from an Ardipithecus-like most recent common ancestor (MRCA); (2) indication of some degree of climbing ability; (3) allometry. Recent discoveries of other partial skeletons of Australopithecus, such as those of A. sediba (MH1 and MH2) and A. afarensis (KSD-VP-1/1 and DIK-1/1), have provided new opportunities to test hypotheses of early hominin body size and limb proportions. Yet, no early hominin is as complete (>90%), as is the 3.67 Ma Little Foot (StW 573) specimen, from Sterkfontein Member 2. Here, we provide the first descriptions of its upper and lower long limb bones, as well as a comparative context of its limb proportions. As to the latter, we found that StW 573 possesses absolutely longer limb lengths than A.L. 288-1, but both skeletons show similar limb proportions. This finding seems to argue against an allometric explanation for the limb proportions of A.L. 288-1. In fact, our multivariate allometric analysis suggests that limb lengths of Australopithecus, as represented by StW 573 and A.L. 288-1, developed along a significantly different (p < 0.001) allometric scale than that which typifies modern humans and African apes. Our analyses also suggest, as have those of others, that hominin limb evolution occurred in two stages with: (1) a modest increase in lower limb length and a concurrent shortening of the antebrachium between Ardipithecus and Australopithecus, followed by (2) considerable lengthening of the lower limb along with a decrease of both upper limb elements occurring between Australopithecus and Homo sapiens.


1981 ◽  
Vol 54 (3) ◽  
pp. 421-430 ◽  
Author(s):  
Charles E. Oxnard ◽  
Rebecca German ◽  
Francoise-K. Jouffroy ◽  
Jacques Lessertisseur

1988 ◽  
Vol 36 (3) ◽  
pp. 251 ◽  
Author(s):  
ME Finch ◽  
L Freedman

The limb bones and girdles of an almost complete specimen of the extinct 'marsupial lion' Thylacoleo carnifex, from Moree, New South Wales, have been fully described pictorially, metrically and in text. To investigate limb function, intra- and inter-limb segment indices and limb proportions standardised against the presacral vertebral column, were calculated for 11 samples of extant Australian marsupials. Comparisons were made between these values, those for Thylacoleo and published data for extant placental carnivores. The Thylacoleo fore- and hindlimbs were almost equal in length (FL/HL, 94%) and relatively long compared to the vertebral column (79% and 84%). In the forelimb the radius was clearly longer than the humerus (115%), and the hindlimb the tibia was considerably shorter than the femur (82%). Amongst the marsupials, the main Thylacoleo indices were most similar to those of Sarcophilus, but with some significant differences, notably in propodial/epipodial length ratios. Compared to Panthera leo there were many marked similarities. Morphologically, the Thylacoleo scapula conforms to that found in walking and trotting, rather than climbing, viverrids; the pelvis similarly agrees with that of ambulators and cursors. It was concluded that Thylacoleo carnifex was a slow- medium cursor, possibly capable of leaping. There was also a series of adaptations such as the length of the radius, the stout olecranon, the blade-like fifth metatarsal and the massive terminal phalanx of digit I, clearly implying a carnivorous habit.


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