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      The Cortical Topography of Visual Evoked Potentials Elicited by Chromatic and Luminance Motion

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          Abstract

          When motion-onset VEPs are elicited by moving luminance patterns, the motion specific component of the response, N2, is more prominent at electrode sites that overlay the lateral occipito-parietal cortex close to area V5/MT, than over the primary visual cortex. Functional segregation suggests that colour and motion processing should take place along different ventral occipito-temporal and lateral occipito-parietal pathways, respectively. Hence, a different topographical distribution might be expected for the motion-onset VEPs elicited by chromatic and luminance motion stimuli. We recorded motion-onset VEPs to moving luminance or isoluminant chromatic sinusoidal grating stimuli from five electrodes sites located at Oz, and at four locations (T1-T4) lateral to Oz, at intervals of 5% of the head circumference. Responses were recorded from 6 subjects over a range of speeds and contrasts. The results showed that the N2 component was maximal at similar lateral electrode locations (T2) for both luminance-defined and chromatically-defined motion. The earlier P1 component was of greatest magnitude at the occipital pole (Oz) and decreased with more lateral electrode placement and again this was the same for colour and luminance responses. These similarities suggest a common origin for VEPs elicited by colour and luminance defined motion.

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          Chromatic mechanisms in lateral geniculate nucleus of macaque.

          This paper introduces a new technique for the analysis of the chromatic properties of neurones, and applies it to cells in the lateral geniculate nucleus (l.g.n.) of macaque. The method exploits the fact that for any cell that combines linearly the signals from cones there is a restricted set of lights to which it is equally sensitive, and whose members can be exchanged for one another without evoking a response. Stimuli are represented in a three-dimensional space defined by an axis along which only luminance varies, without change in chromaticity, a 'constant B' axis along which chromaticity varies without changing the excitation of blue-sensitive (B) cones, a 'constant R & G' axis along which chromaticity varies without change in the excitation of red-sensitive (R) or green-sensitive (G) cones. The orthogonal axes intersect at a white point. The isoluminant plane defined by the intersection of the 'constant B' and 'constant R & G' axes contains lights that vary only in chromaticity. In polar coordinates the constant B axis is assigned the azimuth 0-180 deg, and the constant R & G axis the azimuth 90-270 deg. Luminance is expressed as elevation above or below the isoluminant plane (-90 to +90 deg). For any cell that combines cone signals linearly, there is one plane in this space, passing through the white point, that contains all lights that can be exchanged silently. The position of this 'null plane' provides the 'signature' of the cell, and is specified by its azimuth (the direction in which it intersects the isoluminant plane of the stimulus space) and its elevation (its angle of inclination to the isoluminant plane). A colour television receiver was used to produce sinusoidal gratings whose chromaticity and luminance could be modulated along any vector passing through the white point in the space described. The spatial and temporal frequencies of modulation could be varied over a large range. When stimulated by patterns of low spatial and low temporal frequency, two groups of cells in the parvocellular laminae of the l.g.n. were distinguished by the locations of their null planes. The null planes of the larger group were narrowly distributed about an azimuth of 92.6 deg and more broadly about an elevation of 51.5 deg, which suggests that they receive opposed, but not equally balanced, inputs from only R and G cones. These we call R-G cells.(ABSTRACT TRUNCATED AT 400 WORDS)
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            Functional analysis of human MT and related visual cortical areas using magnetic resonance imaging.

            Using noninvasive functional magnetic resonance imaging (fMRI) technique, we analyzed the responses in human area MT with regard to visual motion, color, and luminance contrast sensitivity, and retinotopy. As in previous PET studies, we found that area MT responded selectively to moving (compared to stationary) stimuli. The location of human MT in the present fMRI results is consistent with that of MT in earlier PET and anatomical studies. In addition we found that area MT has a much higher contrast sensitivity than that in several other areas, including primary visual cortex (V1). Functional MRI half-amplitudes in V1 and MT occurred at approximately 15% and 1% luminance contrast, respectively. High sensitivity to contrast and motion in MT have been closely associated with magnocellular stream specialization in nonhuman primates. Human psychophysics indicates that visual motion appears to diminish when moving color-varying stimuli are equated in luminance. Electrophysiological results from macaque MT suggest that the human percept could be due to decreases in firing of area MT cells at equiluminance. We show here that fMRI activity in human MT does in fact decrease at and near individually measured equiluminance. Tests with visuotopically restricted stimuli in each hemifield produced spatial variations in fMRI activity consistent with retinotopy in human homologs of macaque areas V1, V2, V3, and VP. Such activity in area MT appeared much less retinotopic, as in macaque. However, it was possible to measure the interhemispheric spread of fMRI activity in human MT (half amplitude activation across the vertical meridian = approximately 15 degrees).
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              Spectral sensitivity of the foveal cone photopigments between 400 and 500 nm.

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                Author and article information

                Journal
                Open Ophthalmol J
                TOOPHTJ
                The Open Ophthalmology Journal
                Bentham Science Publishers Ltd.
                1874-3641
                17 December 2007
                2007
                : 1
                : 25-34
                Affiliations
                []Vision Science Research Group, School of Life Sciences, University of Bradford, Richmond Road, Bradford BD7 1DP, UK
                Author notes
                [* ]Address correspondence to this author at the Division of Optometry, School of Life Sciences, University of Bradford, Bradford, BD7 1DP, UK; Tel: +44 (0)1274 234648; Fax: +44 (0)1274 235570; E-mail: d.mckeefry@ 123456bradford.ac.uk
                Article
                TOOPHTJ
                10.2174/1874364100701010025
                2605699
                19478864
                774dcebe-6bfb-4d4c-8db4-db77d00f8d87
                2007 Bentham Science Publishers Ltd.

                This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.5/) which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 2 November 2007
                : 23 November 2007
                : 3 December 2007
                Categories
                Article

                Ophthalmology & Optometry
                motion,visual evoked potentials (veps).,colour
                Ophthalmology & Optometry
                motion, visual evoked potentials (veps)., colour

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