Brain Evolution: Mammals, Primates, Chimpanzees, and Humans

作者: Charles E. Oxnard

DOI: 10.1023/B:IJOP.0000043355.96393.8B

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摘要: Though many modern techniques are available for studying brains, they difficult to use in evolutionary contexts that require examination of large numbers specimens and species, all major parts the brain. Thus, studies species whole brains still tend be based upon simpler data such as sizes brain components. Such investigations, carried out over decades, have usually employed univariate bivariate analyses, though a few investigators used early multivariate methods. In mammals, these generally show primacy relationship between brain-part with overall body size. More recent applications confirmed this (Finlay, B. L., Darlington, R. (1995). Science 268: 1578–1584) some also separated highest level phylogenetic groups: strepsirrhines haplorrhines (Barton, A., Harvey, P. H. (2000). Nature 405: 1055–1058). Both findings were, fact, evident earlier (Holloway, L. (1979). Hahn, M. E., Jensen C., Dudek, C. (eds.), Development Evolution Brain Size: Behavioral Implications, Academic Press, New York, pp. 59–88; Sacher, G. A. (1970). Noback, R., Montagna, W. The Primate Brain: Advances Primatology. Vol. 1, Appleton-Century-Crofts, Educational Division, Meredith Corporation, 245–287). However, new employing proportional aimed at conveying input/output relationships components further groupings share convergences lifestyles (de Winter, W., Oxnard, E. (2001). 409: 710–714). brought about by combinations variables seem associated functions implied specific lifestyles. Our most results demonstrate chimpanzees humans especially different from one another, difference is not due size alone. Part merely continuation, towards humans, trend already present across other primates relates mainly neocortical increase. But several independent differences direction primate trend, but mammals examined including nonhuman primates. latter related simply enhancement neocortex, reflect internal relationships. separation so it goes far beyond conventional 98.6% commonality their DNAs. It fits better more molecular, developmental implying considerably greater than recognized.

参考文章(25)
D. Normile, Gene Expression Differs in Human and Chimp Brains Science. ,vol. 292, pp. 44- 45 ,(2001) , 10.1126/SCIENCE.292.5514.44
Robert A. Barton, Paul H. Harvey, Mosaic evolution of brain structure in mammals Nature. ,vol. 405, pp. 1055- 1058 ,(2000) , 10.1038/35016580
Willem de Winter, Charles E. Oxnard, Evolutionary radiations and convergences in the structural organization of mammalian brains Nature. ,vol. 409, pp. 710- 714 ,(2001) , 10.1038/35055547
P. Thomas Schoenemann, Brain scaling, behavioral ability, and human evolution Behavioral and Brain Sciences. ,vol. 24, pp. 293- 295 ,(2001) , 10.1017/S0140525X01383954
Ulfur Arnason, Anette Gullberg, Alondra Schweizer Burguete, Axel Janice, Molecular estimates of primate divergences and new hypotheses for primate dispersal and the origin of modern humans. Hereditas. ,vol. 133, pp. 217- 228 ,(2004) , 10.1111/J.1601-5223.2000.00217.X
Heinz Stephan, Heiko Frahm, Georg Baron, New and Revised Data on Volumes of Brain Structures in Insectivores and Primates Folia Primatologica. ,vol. 35, pp. 1- 29 ,(1981) , 10.1159/000155963
Ralph L. Holloway, The O.H. 7 (Olduvai Gorge, Tanzania) hominid partial brain endocast revisited American Journal of Physical Anthropology. ,vol. 53, pp. 267- 274 ,(1980) , 10.1002/AJPA.1330530211
Barbara L. Finlay, Richard B. Darlington, Nicholas Nicastro, Developmental structure in brain evolution. Behavioral and Brain Sciences. ,vol. 24, pp. 263- 278 ,(2001) , 10.1017/S0140525X01003958
B. Finlay, R. Darlington, Linked regularities in the development and evolution of mammalian brains Science. ,vol. 268, pp. 1578- 1584 ,(1995) , 10.1126/SCIENCE.7777856