Color differences scaled by chromatic modulation sensitivity functions.

In this paper we present the results of an analysis of the physically measured surface reflectance spectra of 360 matte Munsell chromatic color chips plus 10 flat achromatic vectors corresponding to Munsell value levels 10 (white) to 1 (near black) for a total sample size of 370. Each of the 370 spectra was multiplied by the spectral radiant power distribution of D65 light so that the final results represent the spectra of reflected light from Munsell color chips under D65 illumination. We simultaneously model the structure of the color chips and the spectra in a common three-dimensional Euclidean space, oriented to yield the most interpretable structure with respect of the Munsell color structure. In this orientation, axis 1 roughly corresponds to the mean power of the spectral reflectance (approximate Munsell value), axis 2 goes from Munsell red to blue-green, and axis 3 goes from Munsell green-yellow to purple. Basis factors for the spectra are also plotted against wavelength and Munsell hue. These plots have implications for theories of opponent processes. By plotting the chips and spectra in the same space we obtain virtually exact correspondences between the various Munsell hues and spectral values in nanometers for comparison to those obtained by previous researchers. Mathematical derivations are provided to validate the common Euclidean model.

Color Perception↗

PubMed2002

The relationship between cortical activation and perception investigated with invisible stimuli.

The aim of this work was to study the relationship between cortical activity and visual perception. To do so, we developed a psychophysical technique that is able to dissociate the visual percept from the visual stimulus and thus distinguish brain activity reflecting the perceptual state from that reflecting other stages of stimulus processing. We used dichoptic color fusion to make identical monocular stimuli of opposite color contrast "disappear" at the binocular level and thus become "invisible" as far as conscious visual perception is concerned. By imaging brain activity in subjects during a discrimination task between face and house stimuli presented in this way, we found that house-specific and face-specific brain areas are always activated in a stimulus-specific way regardless of whether the stimuli are perceived. Absolute levels of cortical activation, however, were lower with invisible stimulation compared with visible stimulation. We conclude that there is no terminal "perceptual" area in the visual brain, but that the brain regions involved in processing a visual stimulus are also involved in its perception, the difference between the two being dictated by a higher level of activity in the specific brain region when the stimulus is perceived.

Color Perception↗

PubMed2002

Determinants of asynchronous processing in vision.

When a stimulus oscillates in both colour and direction of motion, changes in colour must lag behind those in direction if they are to be seen as concurrent. It has been argued that this lag is the consequence of asynchronous visual processing, with colour being processed more rapidly than motion. This proposal is contentious: it has been criticized on the basis that the time-course of cortical activity may not correlate directly with that of perceptual experience. Here, we demonstrate that the extent of the apparent asynchrony can vary according to the prevailing stimulus conditions. The apparent asynchrony is greatest if the stimulus is composed of opponent directions of motion and is reduced if the angular difference between the directions is reduced. This pattern of results suggests that asynchronous neural activity arises, in part, as a consequence of differential levels of inhibition within relatively independent cortical structures.

Color Perception↗