scholarly journals The position of Australopithecus sediba within fossil hominin hand use diversity

2020 ◽  
Vol 4 (7) ◽  
pp. 911-918 ◽  
Author(s):  
Christopher J. Dunmore ◽  
Matthew M. Skinner ◽  
Ameline Bardo ◽  
Lee R. Berger ◽  
Jean-Jacques Hublin ◽  
...  
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2018 ◽  
Vol 30 (1-2) ◽  
pp. 32-48
Author(s):  
M. Louail ◽  
S. Prat

The standard ASUDAS scoring system (Arizona State University Dental Anthropology System) is used to assess dental morphological variations in modern humans. It is also frequently used to study, score, and compare morphological variations in fossil hominin taxa and to examine their phylogenetic relationships. However, using ASUDAS in studies of this type is under debate because it is based on modern Homo sapiens populations and does not appear to cover all variations observed in fossil Plio-Pleistocene homi- nins. Our observations and coding of 178 dentals casts of Plio-Pleistocene specimens based on ASUDAS and from the literature have confirmed the need to adapt the standard system to fossil hominins. In this initial study, we propose that the scoring procedures for some morphological characters need to be readjusted, while others could be standardized following the ASUDAS system.


2014 ◽  
Vol 154 (2) ◽  
pp. 201-214 ◽  
Author(s):  
Marina Elliott ◽  
Helen Kurki ◽  
Darlene A. Weston ◽  
Mark Collard

2017 ◽  
Vol 112 ◽  
pp. 93-104 ◽  
Author(s):  
Kevin G. Hatala ◽  
Neil T. Roach ◽  
Kelly R. Ostrofsky ◽  
Roshna E. Wunderlich ◽  
Heather L. Dingwall ◽  
...  
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1998 ◽  
Vol 193 (1) ◽  
pp. 61-72 ◽  
Author(s):  
BERNARD WOOD ◽  
LESLIE AIELLO ◽  
CHRISTOPHER WOOD ◽  
CATHY KEY
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2017 ◽  
Author(s):  
Ian Towle ◽  
Joel D. Irish ◽  
Marina Elliott ◽  
Isabelle De Groote

AbstractTooth root grooves and other ante-mortem dental tissue loss not associated with caries found on or near the cementoenamel junction (CEJ) are commonly termed non-carious cervical lesions. Three main processes are implicated in forming these lesions: abrasion, dental erosion, and abfraction. As yet, these lesions have not been described in non-Homo hominins. In this study South African fossil hominin collections were examined for evidence of any type of non-carious cervical lesion. Only one individual shows ante-mortem root grooves consistent with non-carious cervical lesions. Two teeth, a mandibular right permanent lateral incisor (STW 270) and canine (STW 213), belonging to the same Australopithecus africanus individual, show clear ante-mortem grooves on the labial root surface. These lesions start below the CEJ, extend over a third of the way toward the apex, and taper to a point towards the lingual side. Microscopic examination revealed no clear directional striations. The shape of these grooves is extremely similar to clinical examples of dental erosion, with the lack of striations supporting this diagnosis. These are the oldest hominin examples of non-carious cervical lesions and first described in a genus other than Homo; further, the lesions suggest that this individual regularly consumed or processed acidic food items.


Author(s):  
Tracy L. Kivell ◽  
Kelly R. Ostrofsky ◽  
Brian G. Richmond ◽  
Michelle S.M. Drapeau

This chapter presents description and analysis of the metacarpals and manual phalanges from Sterkfontein. Although the morphology is generally similar across the sample where there are duplicates of the same element, there are differences in size that are quite remarkable within the context of all South African hominins. Some very large specimens suggest the presence of individuals at Sterkfontein with much larger hands, and presumably larger body size, at Sterkfontein than those of A. sediba MH2, H. naledi and the Swartkrans hominins. Australopithecus africanus had human-like proportions, but this may be plesiomorphic within the hominoid clade. The potentially less mobile trapezium-Mc1 joint, absence of a fully developed palmar pulp on the distal thumb, more limited pronation of the index finger, and potentially more wedge-shaped trapezoid inferred from the preserved external morphology, is consistent with lower manipulative loading of the thumb than is typical of later Homo. As for other forelimb elements, moderately curved manual phalanges suggests a greater reliance on forelimb-dominated locomotor behaviors and perhaps selection for more frequent use of an arboreal environment in A. africanus than is found in A. afarensis. Thus, within this broader context, the Sterkfontein fossil hominin remains are not unusual. The Sterkfontein hand fossils suggest an overall manipulative and locomotor loading regime that was more similar to that of other South African australopiths and distinct from that of later Homo, but more refined functional interpretations require additional fossil evidence, particularly from associated hand skeletons


2019 ◽  
Vol 98 (4) ◽  
pp. 398-405 ◽  
Author(s):  
P.S. Ungar

Paleontologists use fossil teeth to reconstruct the diets of early hominins and other extinct species. Some evidence is adaptive: nature selects for tooth size, shape, and structure best suited to specific food types. Other evidence includes traces left by actual foods eaten, such as microscopic tooth wear. This critical review considers how molars work, how they are used, and how occlusal topography and dental microwear can be used to infer diet and food preferences in the past, particularly for hominins of the Pliocene and early Pleistocene. Understanding that cheek teeth function as guides for chewing and tools for fracturing allows us to characterize aspects of occlusal form that reflect mechanical properties of foods to which a species is adapted. Living primates that often eat leaves, for example, have longer crests and more sloping occlusal surfaces than those that prefer hard foods. Studies of feeding ecology have shown, however, that tooth shape does not always correspond to preferred food items. It often follows mechanically challenging foods whether eaten often or rarely. Other lines of evidence that reflect actual tooth use are required to work out food preferences. Microwear textures, for example, reflect foods eaten by individuals in the past such that hard seeds and bone tend to leave complex, pitted surface textures, whereas tough leaves and meat more often leave anisotropic ones covered in long, parallel scratches. The study of fossil hominin molars shows how these various attributes are combined to infer diet and food preference in the past. A trend in occlusal morphology suggests decreased dietary specialization from Australopithecus to early Homo, and increasing dispersion in microwear complexity values is consistent with this. On the other hand, occlusal morphology may suggest dietary specialization in Paranthropus, although different species of this genus have different microwear texture patterns despite similar craniodental adaptations.


2018 ◽  
Vol 114 (3/4) ◽  
Author(s):  
Chris Robinson ◽  
Timothy L. Campbell ◽  
Susanne Cote ◽  
Darryl J. de Ruiter

In attempting to resolve the phylogenetic relationships of fossil taxa, researchers can use evidence from two sources – morphology and known temporal ranges. For most taxa, the available evidence is stronger for one of these data sources. We examined the limitations of temporal data for reconstructing hominin evolutionary relationships, specifically focusing on the hypothesised ancestor–descendant relationship between Australopithecus sediba and the genus Homo. Some have implied that because the only known specimens of A. sediba are dated to later than the earliest fossils attributed to Homo, the former species is precluded from being ancestral to the latter. However, A. sediba is currently known from one site dated to 1.98 Ma and, thus, its actual temporal range is unknown. Using data from the currently known temporal ranges of fossil hominin species, and incorporating dating error in the analysis, we estimate that the average hominin species’ temporal range is ~0.97 Myr, which is lower than most figures suggested for mammalian species generally. Using this conservative figure in a thought experiment in which the Malapa specimens are hypothesised to represent the last appearance date, the middle of the temporal range, and first appearance date for the species, the first appearance date of A. sediba would be 2.95, 2.47 and 1.98 Ma, respectively. As these scenarios are all equally plausible, and 2.95 Ma predates the earliest specimens that some have attributed to Homo, we cannot refute the hypothesis that the species A. sediba is ancestral to our genus based solely on currently available temporal data.


2019 ◽  
pp. 341-359 ◽  
Author(s):  
Ella Been ◽  
Tatiana Waintraub ◽  
Asier Gómez-Olivencia ◽  
Leonid Kalichman ◽  
Patricia Ann Kramer ◽  
...  
Keyword(s):  
3D Model ◽  

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