Brain size/Bibliography: Difference between revisions

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*{{CZ:Ref:Kremen 2009 Genetic and environmental influences on the size of specific brain regions in midlife - The VETSA MRI study}}
*{{CZ:Ref:Isler 2009 Why are there so few smart mammals (but so many smart birds)?}}
*{{CZ:Ref:Isler 2009 Why are there so few smart mammals (but so many smart birds)?}}
*{{:CZ:Ref:DOI:10.1086/589461}}
*{{CZ:Ref:DOI:10.1086/589461}}
*{{:CZ:Ref:DOI:10.1016/j.brainres.2007.09.032}}
*{{CZ:Ref:DOI:10.1016/j.brainres.2007.09.032}}
*{{CZ:Ref:Healy 2007 A critique of comparative studies of brain size}}
*{{CZ:Ref:Healy 2007 A critique of comparative studies of brain size}}
*{{CZ:Ref:Morand-Ferron 2007 Food stealing in birds: brain or brawn?}}
*{{CZ:Ref:Morand-Ferron 2007 Food stealing in birds: brain or brawn?}}
*{{:CZ:Ref:DOI:10.1073/pnas.0606337103}}
*{{CZ:Ref:DOI:10.1073/pnas.0606337103}}
*{{:CZ:Ref:DOI:10.1073/pnas.0605843103}}
*{{CZ:Ref:DOI:10.1073/pnas.0605843103}}
*{{CZ:Ref:Pitnick 2006 Mating system and brain size in bats}}
*{{CZ:Ref:Pitnick 2006 Mating system and brain size in bats}}
*{{CZ:Ref:Schillaci 2006 Sexual Selection and the Evolution of Brain Size in Primates}}
*{{CZ:Ref:Schillaci 2006 Sexual Selection and the Evolution of Brain Size in Primates}}
*{{:CZ:Ref:DOI:10.1159/000094088}}
*{{CZ:Ref:DOI:10.1159/000094088}}
*{{:CZ:Ref:DOI:10.1016/j.ceb.2005.11.004}}
*{{CZ:Ref:DOI:10.1016/j.ceb.2005.11.004}}
*{{CZ:Ref:Kruska 2005 On the Evolutionary Significance of Encephalization in Some Eutherian Mammals: Effects of Adaptive Radiation, Domestication, and Feralization}}
*{{CZ:Ref:Kruska 2005 On the Evolutionary Significance of Encephalization in Some Eutherian Mammals: Effects of Adaptive Radiation, Domestication, and Feralization}}
*{{CZ:Ref:Safi 2005 Bigger is not always better: when brains get smaller}}
*{{CZ:Ref:Safi 2005 Bigger is not always better: when brains get smaller}}
*{{:CZ:Ref:DOI:10.1038/nature03651‎}}
*{{CZ:Ref:DOI:10.1038/nature03651‎}}
*{{CZ:Ref:Lefebvre 2004 Brains, Innovations and Evolution in Birds and Primates}}
*{{CZ:Ref:Lefebvre 2004 Brains, Innovations and Evolution in Birds and Primates}}
*{{:CZ:Ref:DOI:10.1016/j.neuron.2004.09.023}}
*{{CZ:Ref:DOI:10.1016/j.neuron.2004.09.023}}
*{{:CZ:Ref:DOI:10.1194/jlr.R400004-JLR200}}
*{{CZ:Ref:DOI:10.1194/jlr.R400004-JLR200}}
*{{:CZ:Ref:DOI:10.1023/A:1024178127195}}
*{{CZ:Ref:DOI:10.1023/A:1024178127195}}
*{{:CZ:Ref:Clark2001sam}}
*{{CZ:Ref:Clark2001sam}}
*{{:CZ:Ref:DOI:10.1006/jhev.1999.0313}}
*{{CZ:Ref:DOI:10.1006/jhev.1999.0313}}
*{{CZ:Ref:Hladik 1999 On Diet and Gut Size in Non-human Primates and Humans: is There a Relationship to Brain Size?}}
*{{CZ:Ref:Hladik 1999 On Diet and Gut Size in Non-human Primates and Humans: is There a Relationship to Brain Size?}}
*{{:CZ:Ref:DOI:10.1111/j.1440-1681.1998.tb02289.x}}
*{{CZ:Ref:DOI:10.1111/j.1440-1681.1998.tb02289.x}}
*{{:CZ:Ref:DOI:10.1002/(SICI)1096-9861(19970728)384:2 ^312::AID-CNE10^ 3.0.CO;2-K}}
*{{CZ:Ref:DOI:10.1002/(SICI)1096-9861(19970728)384:2 ^312::AID-CNE10^ 3.0.CO;2-K}}
*{{CZ:Ref:Aiello 1995 The Expensive-Tissue Hypothesis: the Brain and the Digestive System in Human and Primate Evolution}}
*{{CZ:Ref:Aiello 1995 The Expensive-Tissue Hypothesis: the Brain and the Digestive System in Human and Primate Evolution}}
*{{CZ:Ref:Ridley 1995 Pelvic sexual dimorphism and relative neonatal brain size really are related}}
*{{CZ:Ref:Ridley 1995 Pelvic sexual dimorphism and relative neonatal brain size really are related}}
*{{:CZ:Ref:DOI:10.1046/j.1420-9101.1993.6020209.x}}
*{{CZ:Ref:DOI:10.1046/j.1420-9101.1993.6020209.x}}
*{{:CZ:Ref:DOI:10.1002/cne.900590102}}
*{{CZ:Ref:DOI:10.1002/cne.900590102}}

Revision as of 03:57, 20 October 2009

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A list of key readings about Brain size.
Please sort and annotate in a user-friendly manner. For formatting, consider using automated reference wikification.
Builds on the expensive tissue hypothesis proposed by Aiello & Wheeler (1995) and provides evidence that the maximum rate of population increase, as defined by Cole (1954), is correlated negatively with brain size in mammals and birds, as long as parental care is not provided (and thus the energetic costs of feeding borne) by the mothers alone. Predicts that such allomaternal care increases the "maximum viable brain size" in a given family and that brain size evolution is strongly coupled to mass extinction events.
Based on data about brain size and body size in 120 families of birds, this study shows by means of path analysis that about 12% of within-family body size disparity can be explained by the average residual brain size within that family. Based on observations that brain size correlates with a number of cognitive measures, it is then concluded that behaviour might contribute to evolutionary diversification.
Provides a literature review based on "856 reports of interspecific kleptoparasitism by 197 species from 33 avian families", concluding that this behaviour correlates with brain size (and hence cognition), habitat and diet but not with body size or aggression.
Provides comparative histological data on the glia-neuron ratios in prefrontal area 9L of the neocortex in 18 anthropoid primate species and on the allometric scaling of this ratio with brain size, concluding that the value in humans is well within the range allometrically expected for an anthropoid primate with our brain size.
Shows a correlation between brain size and monogamy in primates.
Based on the analysis of published data on body mass, wing area and absolute brain size in 104 species of bats, the authors conclude that brain size is a trade-off between cognitive requirements imposed by the natural or social environment, and energetic constraints, particularly in relation to flight.
Proposed that the energetic costs of the resting metabolism of different organs within the body have to be balanced. Specifically, such a trade-off is hypothesized to have governed the increasing brain size during primate and human evolution, in concert with a decrease in the amount of digestive tissue. For a critique, see Hladik et al. (1999).