Three-dimensional structure and evolution of primate primary visual cortex.

In this study, three-dimensional reconstructions of primate primary visual cortex (V1) were used to address questions about its evolution. The three-dimensional shape of V1 in anthropoids is significantly longer and narrower than in strepsirrhines. This difference is an effect of clade and is not due to differences in activity pattern or V1 size. New measurements of V1 volume were also provided in order to reassess V1 size differences between strepsirrhines and anthropoids. It was found that for a given lateral geniculate nucleus (LGN) volume, anthropoids have a significantly larger V1 than strepsirrhines do. This is important since LGN is the principal source of V1's input. Finally, independent contrasts analysis was used to examine the scaling of V1 relative to LGN, the rest of cortex, and the rest of the brain. It was confirmed that V1 scales with positive allometry relative to LGN. A number of possible explanations for scaling are discussed. V1 scaling may have to do with the tendency of large brains to be more compartmentalized than small brains, or V1 scaling might reflect the geometry of information representation.

[1]  J. Allman,et al.  The scaling of frontal cortex in primates and carnivores. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[2]  Callum F. Ross,et al.  Anthropoid origins : new visions , 2004 .

[3]  J. Allman,et al.  The Distribution and Size of Retinal Ganglion Cells in Microcebus murinus, Cheirogaleus medius, and Tarsius syrichta: Implications for the Evolution of Sensory Systems in Primates , 2004 .

[4]  J. Allman,et al.  The Distribution and Size of Retinal Ganglion Cells in Cheirogaleus medius and Tarsius syrichta : Implications for the Evolution of Sensory Systems in Primates , 2002 .

[5]  Á. Szél,et al.  Short and mid‐wavelength cone distribution in a nocturnal Strepsirrhine primate (Microcebus murinus) , 2001, The Journal of comparative neurology.

[6]  C. Stevens An evolutionary scaling law for the primate visual system and its basis in cortical function , 2001, Nature.

[7]  Callum F. Ross,et al.  Into the Light: The Origin of Anthropoidea , 2000 .

[8]  P. Harvey,et al.  Mosaic evolution of brain structure in mammals , 2000, Nature.

[9]  Jon H. Kaas,et al.  Why is Brain Size so Important:Design Problems and Solutions as Neocortex Gets Biggeror Smaller , 2000 .

[10]  J. Kaas,et al.  Distinctive compartmental organization of human primary visual cortex. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[11]  D. Boire,et al.  Size and distribution of retinal ganglion cells in the St. Kitts green monkey (Cercopithecus aethiops sabeus) , 1997, The Journal of comparative neurology.

[12]  M G Rosa,et al.  Visual field representation in striate and prestriate cortices of a prosimian primate (Galago garnetti). , 1997, Journal of neurophysiology.

[13]  N. Rowe The Pictorial Guide to the Living Primates , 1996 .

[14]  B. Finlay,et al.  Linked regularities in the development and evolution of mammalian brains. , 1995, Science.

[15]  J. Downing,et al.  CRC Handbook of Mammalian Body Masses , 1995 .

[16]  V. Perry,et al.  The retinal ganglion cell distribution and the representation of the visual field in area 17 of the owl monkey, Aotus trivirgatus , 1993, Visual Neuroscience.

[17]  J. Jonas,et al.  Human optic nerve fiber count and optic disc size. , 1992, Investigative ophthalmology & visual science.

[18]  Q. Fischer,et al.  Number and distribution of retinal ganglion cells in anubis baboons (Papio anubis). , 1991, Brain, behavior and evolution.

[19]  B. Boycott,et al.  Retinal ganglion cell density and cortical magnification factor in the primate , 1990, Vision Research.

[20]  A. Hendrickson,et al.  Human photoreceptor topography , 1990, The Journal of comparative neurology.

[21]  C. W. Picanço-Diniz,et al.  Retinal ganglion cell distribution in the cebus monkey: A comparison with the cortical magnification factors , 1989, Vision Research.

[22]  B. E. Reese,et al.  Axon diameter distributions across the monkey's optic nerve , 1988, Neuroscience.

[23]  P. Rakic Specification of cerebral cortical areas. , 1988, Science.

[24]  A. Cowey,et al.  The ganglion cell and cone distributions in the monkey's retina: Implications for central magnification factors , 1985, Vision Research.

[25]  H. Frahm,et al.  Comparison of brain structure volumes in insectivora and primates. V. Area striata (AS). , 1984, Journal fur Hirnforschung.

[26]  H. Frahm,et al.  New and revised data on volumes of brain structures in insectivores and primates. , 1981, Folia primatologica; international journal of primatology.

[27]  V. Casagrande,et al.  The size and topographic arrangement of retinal ganglion cells in the galago , 1980, Vision Research.

[28]  G. H. Jacobs Visual capacities of the owl monkey (Aotus trivirgatus)—II. Spatial contrast sensitivity , 1977, Vision Research.

[29]  J. Kaas,et al.  The sizes and distribution of ganglion cells in the retina of the owl monkey, aotus trivirgatus , 1976, Vision Research.

[30]  F. Sanides 7 – Representation in the Cerebral Cortex and Its Areal Lamination Patterns , 1972 .

[31]  A. Guyton,et al.  Structure and function of the nervous system , 1972 .

[32]  J. Kaas,et al.  Representation of the visual field in striate and adjoining cortex of the owl monkey (Aotus trivirgatus). , 1971, Brain research.

[33]  A. E. Jones The retinal structure of (Aotes trivirgatus) the owl monkey , 1965, The Journal of comparative neurology.

[34]  Charles J. Campbell,et al.  The Retinal Ganglion Cell Layer. , 1965 .

[35]  Donald J. Lyle,et al.  The Retinal Ganglion Cell Layer , 1964 .

[36]  A. K.,et al.  Homo Sapiens , 1947, Nature.

[37]  Peter T. Fox,et al.  Mosaic evolution of brain structure in mammals , 2022 .