scholarly journals Structural and molecular study of the supraspinatus muscle of modern humans (Homo sapiens ) and common chimpanzees (Pan troglodytes )

2018 ◽  
Vol 166 (4) ◽  
pp. 934-940 ◽  
Author(s):  
J. M. Potau ◽  
A. Casado ◽  
M. de Diego ◽  
N. Ciurana ◽  
J. Arias-Martorell ◽  
...  
2020 ◽  
Vol 230 ◽  
pp. 151505
Author(s):  
Mónica Gómez ◽  
Aroa Casado ◽  
Marina De Diego ◽  
Júlia Arias-Martorell ◽  
Juan Francisco Pastor ◽  
...  

2021 ◽  
Author(s):  
Ryan M. Campbell ◽  
Gabriel Vinas ◽  
Maciej Henneberg

By identifying similarity in bone and soft tissue covariation patterns in hominids, it is possible to produce facial approximation methods that are compatible with more than one species of primate. In this study, we conducted an interspecific comparison of the nasomaxillary region in chimpanzees and modern humans with the aim of producing a method for predicting the nasal protrusions of ancient Plio-Pleistocene hominids. We addressed this aim by first collecting and performing regression analyses of linear and angular measurements of nasal cavity length and inclination in modern humans ( Homo  sapiens; n = 72) and chimpanzees ( Pan troglodytes ;  n  = 19), and then by performing a set of out-of-group tests. The first test was performed on two subjects that belonged to the same genus as the training sample, i.e.,  Homo  ( n  = 1) and  Pan  ( n  = 1), and the second test, which functioned as an interspecies compatibility test, was performed on  Pan paniscus  ( n  = 1),  Gorilla gorilla  ( n  = 3),  Pongo pygmaeus  ( n  = 1),  Pongo abelli  ( n  = 1),  Symphalangus syndactylus  ( n  = 3), and  Papio hamadryas  ( n  = 3). We identified statistically significant correlations in both humans and chimpanzees with slopes that displayed homogeneity of covariation. Joint prediction formulae were found to be compatible with humans and chimpanzees as well as all other African great apes, i.e., bonobos and gorillas. The main conclusion that can be drawn from this study is that regression models for approximating nasal projection are homogenous among humans and African apes and can thus be reasonably extended to ancestors leading to these clades.


Author(s):  
Francisco J. Ayala ◽  
Camilo J. Cela-Conde

This chapter deals with the similarities and differences between Homo neanderthalensis and Homo sapiens, by considering genetic, brain, and cognitive evidence. The genetic differentiation emerges from fossil genetic evidence obtained first from mtDNA and later from nuclear DNA. With high throughput whole genome sequencing, sequences have been obtained from the Denisova Cave (Siberia) fossils. Nuclear DNA of a third species (“Denisovans”) has been obtained from the same cave and used to define the phylogenetic relationships among the three species during the Upper Palaeolithic. Archaeological comparisons make it possible to advance a four-mode model of the evolution of symbolism. Neanderthals and modern humans would share a “modern mind” as defined up to Symbolic Mode 3. Whether the Neanderthals reached symbolic Mode 4 remains unsettled.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lison Martinet ◽  
Cédric Sueur ◽  
Satoshi Hirata ◽  
Jérôme Hosselet ◽  
Tetsuro Matsuzawa ◽  
...  

AbstractTechniques used in cave art suggest that drawing skills emerged long before the oldest known representative human productions (44,000 years bc). This study seeks to improve our knowledge of the evolutionary origins and the ontogenetic development of drawing behavior by studying drawings of humans (N = 178, 3- to 10-year-old children and adults) and chimpanzees (N = 5). Drawings were characterized with an innovative index based on spatial measures which provides the degree of efficiency for the lines that are drawn. Results showed that this index was lowest in chimpanzees, increased and reached its maximum between 5-year-old and 10-year-old children and decreased in adults, whose drawing efficiency was reduced by the addition of details. Drawings of chimpanzees are not random suggesting that their movements are constrained by cognitive or locomotor aspect and we cannot conclude to the absence of representativeness. We also used indices based on colors and time and asked children about what they drew. These indices can be considered relevant tools to improve our understanding of drawing development and evolution in hominids.


2014 ◽  
Vol 112 (2) ◽  
pp. 366-371 ◽  
Author(s):  
Habiba Chirchir ◽  
Tracy L. Kivell ◽  
Christopher B. Ruff ◽  
Jean-Jacques Hublin ◽  
Kristian J. Carlson ◽  
...  

Humans are unique, compared with our closest living relatives (chimpanzees) and early fossil hominins, in having an enlarged body size and lower limb joint surfaces in combination with a relatively gracile skeleton (i.e., lower bone mass for our body size). Some analyses have observed that in at least a few anatomical regions modern humans today appear to have relatively low trabecular density, but little is known about how that density varies throughout the human skeleton and across species or how and when the present trabecular patterns emerged over the course of human evolution. Here, we test the hypotheses that (i) recent modern humans have low trabecular density throughout the upper and lower limbs compared with other primate taxa and (ii) the reduction in trabecular density first occurred in early Homo erectus, consistent with the shift toward a modern human locomotor anatomy, or more recently in concert with diaphyseal gracilization in Holocene humans. We used peripheral quantitative CT and microtomography to measure trabecular bone of limb epiphyses (long bone articular ends) in modern humans and chimpanzees and in fossil hominins attributed to Australopithecus africanus, Paranthropus robustus/early Homo from Swartkrans, Homo neanderthalensis, and early Homo sapiens. Results show that only recent modern humans have low trabecular density throughout the limb joints. Extinct hominins, including pre-Holocene Homo sapiens, retain the high levels seen in nonhuman primates. Thus, the low trabecular density of the recent modern human skeleton evolved late in our evolutionary history, potentially resulting from increased sedentism and reliance on technological and cultural innovations.


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