Literature DB >> 8564462

The evolution of isocortex.

J H Kaas1.   

Abstract

There are several reasons why we lack detailed and comprehensive theories of how isocortex evolved in the various lines of mammalian evolution. Although current methods allow cortical areas to be defined with a high degree of assurance, few taxa have been studied in detail, and even the most-studied taxa are incompletely understood. In addition, concepts persist from early studies, based on limited data, that confound current theories, and some theories of isocortical evolution have been based on questionable premises. Nevertheless, some conclusions are clearly supportable. Early mammals had small brains with proportionately little isocortex. Mammals with larger brains and proportionately more isocortex evolved in several lines of descent. All mammals appear to have roughly 20 cortical areas, 'the organs of the brain', in common as retentions from an early ancestor, with primary and secondary sensory fields occupying much of cortex. Some of these cortical areas have been greatly modified in some taxa to become significantly expanded in size, highly laminated structurally, or both. Numbers of areas have increased independently in several branches of mammalian evolution, and the functioning of large brains may be enhanced by having more subdivisions. Finally, over many generations new areas may emerge from old by the formation of functionally distinct modules within areas, followed by the fusion of modules to ultimately form separate ones.

Entities:  

Mesh:

Year:  1995        PMID: 8564462     DOI: 10.1159/000113273

Source DB:  PubMed          Journal:  Brain Behav Evol        ISSN: 0006-8977            Impact factor:   1.808


  21 in total

Review 1.  Thoughts on the development, structure and evolution of the mammalian and avian telencephalic pallium.

Authors:  L Puelles
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2001-10-29       Impact factor: 6.237

2.  Functional analysis of V3A and related areas in human visual cortex.

Authors:  R B Tootell; J D Mendola; N K Hadjikhani; P J Ledden; A K Liu; J B Reppas; M I Sereno; A M Dale
Journal:  J Neurosci       Date:  1997-09-15       Impact factor: 6.167

3.  Integrating databases and expert systems for the analysis of brain structures: connections, similarities, and homologies.

Authors:  Mihail Bota; Michael A Arbib
Journal:  Neuroinformatics       Date:  2004

4.  How does connectivity between cortical areas depend on brain size? Implications for efficient computation.

Authors:  Jan Karbowski
Journal:  J Comput Neurosci       Date:  2003 Nov-Dec       Impact factor: 1.621

5.  Neocortex evolution in primates: the "social brain" is for females.

Authors:  Patrik Lindenfors
Journal:  Biol Lett       Date:  2005-12-22       Impact factor: 3.703

Review 6.  The future of mapping sensory cortex in primates: three of many remaining issues.

Authors:  Jon H Kaas
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2005-04-29       Impact factor: 6.237

7.  Dolphin insula reflects minicolumnar organization of mammalian isocortex.

Authors:  Manuel F Casanova; Juan Trippe; Christopher R Tillquist; Andrew E Switala
Journal:  Transl Neurosci       Date:  2010-01-01       Impact factor: 1.757

8.  Changes in cell-cycle kinetics during the development and evolution of primate neocortex.

Authors:  D R Kornack; P Rakic
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-03       Impact factor: 11.205

9.  Mnemonic neuronal activity in somatosensory cortex.

Authors:  Y D Zhou; J M Fuster
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-17       Impact factor: 11.205

10.  Optical imaging of retinotopic maps in a small songbird, the zebra finch.

Authors:  Nina Keary; Joe Voss; Konrad Lehmann; Hans-Joachim Bischof; Siegrid Löwel
Journal:  PLoS One       Date:  2010-08-04       Impact factor: 3.240

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