How does the visual cortex encode color? I summarize a theory in which cortical double-opponent color neurons perform a role in color constancy and a complementary set of color-luminance neurons function to selectively correct for color fringes induced by chromatic aberration in the eye. The theory may help to resolve an ongoing debate concerning the functional properties of cortical receptive ...

We introduce a representation for color texture using unichrome and opponent features computed from Gabor filter outputs. The unichrome features are computed from the spectral bands independently while the opponent features combine information across different spectral bands at different scales. Opponent features are motivated by color opponent mechanisms in human vision. We present a method fo...

In this paper we present a new wavelet-based coding scheme for the compression of color images at compression ratios up to 100:1. It is originally based on the LZC algorithm of Taubman. The main point of discussion in this paper is the color space used and the combination of a coding scheme with a model of human color vision. We describe two approaches: one is based on the pattern-color separab...

It is widely accepted that human color vision is based on two types of cone-opponent mechanism, one differencing L and M cone types (loosely termed "red-green"), and the other differencing S with the L and M cones (loosely termed "blue-yellow"). The traditional view of the early processing of human color vision suggests that each of these cone-opponent mechanisms respond in a bipolar fashion to...

Early postreceptoral color vision is thought to be organized in terms of two principal axes corresponding to opposing L- and M-cone signals (LvsM) or to S-cone signals opposed by a combination of L- and M-cone signals (SvsLM). These cone-opponent axes are now widely used in studies of color vision, but in most cases the corresponding stimulus variations are defined only theoretically, based on ...

We studied the detection of chromoluminance patterns in the presence of chromoluminance pedestals. We examined how thresholds depend on the color directions of the target and the pedestal. Both targets and pedestals were spatial Gabor patterns (horizontal, 1 cpd) .The patterns were spatially modulated in color, luminance or both. Equidiscrimination contours describe contrast thresholds for targ...

We have studied how contrast threshold sensitivity depends jointly on pattern and color. We measured sensitivity to colored Gabor patches from 0.5 to 8 c/deg. At each spatial frequency, we measured in many different color directions. We analyze the sensitivity measurements using a series of nested models. We conclude that a model consisting of three pattern-color separable mechanisms predicts d...