Color and contrast sensitivity in the lateral geniculate body and primary visual cortex of the macaque monkey

We tested color and contrast sensitivity in the magnocellular and parvocellular subdivisions of the lateral geniculate body and in layers 2, 3, 4B, and 4C alpha of visual area 1 to obtain physiological data on the degree of segregation of the 2 pathways and on the fate of the color and contrast information as it is transmitted from the geniculate to the cortex. On average, magnocellular geniculate cells were much less responsive than parvocellular cells to shifts between 2 equiluminant colors. Nevertheless, many magnocellular cells (though not all) continued to give some response at equiluminance. As expected from previous studies, luminance contrast sensitivity differed markedly between magnocellular and parvocellular layers. In V-1, the properties of cells in the magnorecipient layers 4C alpha and 4B faithfully reflected the properties of magnocellular geniculate cells, showing no evidence of any parvocellular input. Like magnocellular geniculate cells, they showed high contrast sensitivity, and with color contrast stimuli they showed large response decrements at equiluminance. In the interblob regions of cortical layers 2 and 3, which anatomically appear to receive most of their inputs from parvorecipient layer 4C beta, contrast sensitivities of some of the cells were compatible with a predominantly parvocellular input. Other interblob cells had sensitivities intermediate between magno- and parvocellular geniculate cells, suggesting a possible contribution from the magnocellular system. Many cells in cortical layers 2 and 3 responded to color- contrast borders equally well at all relative brightnesses of the 2 colors, including equiluminance. We recorded from many direction- and disparity-selective cells in V-1: most of the direction-selective and all of the clearly stereo-selective cells were located in layer 4B.

[1]  D. Hubel Single unit activity in striate cortex of unrestrained cats , 1959, The Journal of physiology.

[2]  R. L. Valois,et al.  Analysis of response patterns of LGN cells. , 1966, Journal of the Optical Society of America.

[3]  D. Hubel,et al.  Spatial and chromatic interactions in the lateral geniculate body of the rhesus monkey. , 1966, Journal of neurophysiology.

[4]  P. Gouras Identification of cone mechanisms in monkey ganglion cells , 1968, The Journal of physiology.

[5]  P Gouras,et al.  Antidromic responses of orthodromically identified ganglion cells in monkey retina , 1969, The Journal of physiology.

[6]  D. Hubel,et al.  Stereoscopic Vision in Macaque Monkey: Cells sensitive to Binocular Depth in Area 18 of the Macaque Monkey Cortex , 1970, Nature.

[7]  D. Hubel,et al.  Laminar and columnar distribution of geniculo‐cortical fibers in the macaque monkey , 1972, The Journal of comparative neurology.

[8]  J. Lund Organization of neurons in the visual cortex, area 17, of the monkey (Macaca mulatta) , 1973, The Journal of comparative neurology.

[9]  R. L. Valois,et al.  Psychophysical studies of monkey vision. I. Macaque luminosity and color vision tests. , 1974, Vision research.

[10]  S. Zeki Cells responding to changing image size and disparity in the cortex of the rhesus monkey , 1974, The Journal of physiology.

[11]  P. Gouras,et al.  Functional properties of ganglion cells of the rhesus monkey retina. , 1975, The Journal of physiology.

[12]  J. Lund,et al.  Interlaminar connections and pyramidal neuron organisation in the visual cortex, area 17, of the Macaque monkey , 1975 .

[13]  S. Anstis,et al.  Illusory reversal of visual depth and movement during changes of contrast , 1975, Vision Research.

[14]  J. Lund,et al.  The origin of efferent pathways from the primary visual cortex, area 17, of the macaque monkey as shown by retrograde transport of horseradish peroxidase , 1975, The Journal of comparative neurology.

[15]  G. Poggio,et al.  Binocular interaction and depth sensitivity in striate and prestriate cortex of behaving rhesus monkey. , 1977, Journal of neurophysiology.

[16]  E. Yund,et al.  Responses of macaque lateral geniculate cells to luminance and color figures. , 1977, Sensory processes.

[17]  M. Ogren,et al.  The neurological organization of pathways between the dorsal lateral geniculate nucleus and visual cortex in old world and new world primates , 1978, The Journal of comparative neurology.

[18]  P. Schiller,et al.  Functional specificity of lateral geniculate nucleus laminae of the rhesus monkey. , 1978, Journal of neurophysiology.

[19]  J K Krüger Responses to wavelength contrast in the afferent visual systems of the cat and the rhesus monkey. , 1979, Vision research.

[20]  P. Gouras,et al.  Responses of cells in foveal visual cortex of the monkey to pure color contrast. , 1979, Journal of neurophysiology.

[21]  M. Wong-Riley Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry , 1979, Brain Research.

[22]  J. Kru¨ger Responses to wavelength contrast in the afferent visual systems of the cat and the rhesus monkey , 1979, Vision Research.

[23]  D. Hubel,et al.  Regular patchy distribution of cytochrome oxidase staining in primary visual cortex of macaque monkey , 1981, Nature.

[24]  R. Scobey Movement sensitivity of retinal ganglion cells in monkey , 1981, Vision Research.

[25]  P. Schiller,et al.  Response properties of single cells in monkey striate cortex during reversible inactivation of individual lateral geniculate laminae. , 1981, Journal of neurophysiology.

[26]  R. Shapley,et al.  Spatial summation and contrast sensitivity of X and Y cells in the lateral geniculate nucleus of the macaque , 1981, Nature.

[27]  R. W. Rodieck,et al.  Retinal ganglion cell classes in the Old World monkey: morphology and central projections. , 1981, Science.

[28]  R. Shapley,et al.  X and Y cells in the lateral geniculate nucleus of macaque monkeys. , 1982, The Journal of physiology.

[29]  D. Hubel,et al.  Thalamic inputs to cytochrome oxidase-rich regions in monkey visual cortex. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[30]  Trichur Raman Vidyasagar,et al.  The responses of cells in macaque lateral geniculate nucleus to sinusoidal gratings. , 1983, The Journal of physiology.

[31]  D. Fitzpatrick,et al.  The laminar organization of the lateral geniculate body and the striate cortex in the squirrel monkey (Saimiri sciureus) , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  Carol L. Colby,et al.  The responses of single cells in the lateral geniculate nucleus of the rhesus monkey to color and luminance contrast , 1983, Vision Research.

[33]  G. Blasdel,et al.  Termination of afferent axons in macaque striate cortex , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[34]  John H. R. Maunsell,et al.  Functional properties of neurons in middle temporal visual area of the macaque monkey. II. Binocular interactions and sensitivity to binocular disparity. , 1983, Journal of neurophysiology.

[35]  G. Blasdel,et al.  Physiological organization of layer 4 in macaque striate cortex , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  D. Baylor,et al.  Spectral sensitivity of single cones in the retina of Macaca fascicularis , 1984, Nature.

[37]  P. Lennie,et al.  Chromatic mechanisms in lateral geniculate nucleus of macaque. , 1984, The Journal of physiology.

[38]  D. Hubel,et al.  Anatomy and physiology of a color system in the primate visual cortex , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[39]  P. Lennie,et al.  Spatial and temporal contrast sensitivities of neurones in lateral geniculate nucleus of macaque. , 1984, The Journal of physiology.

[40]  D. G. Albrecht,et al.  Spatial mapping of monkey VI cells with pure color and luminance stimuli , 1984, Vision Research.

[41]  G. Blasdel,et al.  Intrinsic connections of macaque striate cortex: afferent and efferent connections of lamina 4C , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[42]  P. Lennie,et al.  Spatial frequency analysis in the visual system. , 1985, Annual review of neuroscience.

[43]  J. Charlton,et al.  Response properties of horizontal cells and photoreceptor cells in the retina of the tree squirrel, Sciurus carolinensis. , 1985, Journal of neurophysiology.

[44]  William H. Merigan,et al.  Spatio-temporal vision of macaques with severe loss of Pβ retinal ganglion cells , 1986, Vision Research.

[45]  R. Shapley,et al.  The primate retina contains two types of ganglion cells, with high and low contrast sensitivity. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[46]  D H Hubel,et al.  Connections between layer 4B of area 17 and the thick cytochrome oxidase stripes of area 18 in the squirrel monkey , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[47]  J. Lund Local circuit neurons of macaque monkey striate cortex: I. Neurons of laminae 4C and 5A , 1987, The Journal of comparative neurology.

[48]  DH Hubel,et al.  Segregation of form, color, and stereopsis in primate area 18 , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[49]  E Kaplan,et al.  Contrast affects the transmission of visual information through the mammalian lateral geniculate nucleus. , 1987, The Journal of physiology.

[50]  DH Hubel,et al.  Psychophysical evidence for separate channels for the perception of form, color, movement, and depth , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[51]  The processing of color and luminance information in monkeys: II. Psychophysics , 1987 .

[52]  E. Switkes,et al.  Functional anatomy of macaque striate cortex. IV. Contrast and magno- parvo streams , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[53]  C. R. Michael,et al.  Retinal afferent arborization patterns, dendritic field orientations, and the segregation of function in the lateral geniculate nucleus of the monkey. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[54]  Zenon W. Pylyshyn,et al.  Computational processes in human vision : an interdisciplinary perspective , 1988 .

[55]  Patrick Cavanagh,et al.  Pathways in early vision , 1988 .

[56]  S. Shipp,et al.  The functional logic of cortical connections , 1988, Nature.

[57]  Bb Lee,et al.  Nonlinear summation of M- and L-cone inputs to phasic retinal ganglion cells of the macaque , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[58]  N. Logothetis,et al.  Perceptual deficits and the activity of the color-opponent and broad-band pathways at isoluminance. , 1990, Science.

[59]  N. Logothetis,et al.  Functions of the colour-opponent and broad-band channels of the visual system , 1990, Nature.

[60]  P. Cavanagh,et al.  The contribution of color to motion , 1991 .

[61]  J. Lund,et al.  Local circuit neurons of macaque monkey striate cortex: III. Neurons of laminae 4B, 4A, and 3B , 1997, The Journal of comparative neurology.