The dual role of chromatic backgrounds in color perception.
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Saturation discrimination has been reported to be affected early in the course of a disease. Our empirical data show a compressive curvi-linear relationship between opponent/nonopponent channel activity and saturation thresholds in normal trichromatic observers. This relationship can be explained by a model based on the Hurvich and Jameson saturation coefficient (1957), Psychology Reviews, 64, 384-404. The model considers effects of both selective and nonselective channel losses on saturation processing based on the assumption that disease produces elevated thresholds while maintaining normal psychometric response functions. Both the model and data support clinical observations of saturation losses occurring early in disease. However, the results also indicate that saturation may not be the best modality for monitoring long-term progression of such conditions. We suggest that the different processing characteristics for blue-yellow thresholds may yield added information for saturation testing under some circumstances and that saturation processing occurs at a higher cortical level.
The perceived color of an object depends on the chromaticity of its immediate background. But color appearance is also influenced by remote chromaticities. To quantify these influences, the effects of remote color fields on the appearance of a fixated 2 degrees test field were measured using a forced-choice method. Changes in the appearance of the test field were induced by chromaticity changes of the background and of 2 degrees color fields not adjacent to the test field. The appearance changes induced by the color of the background corresponded to a fraction of between 0.5 and 0.95 of the cone contrast of the background change, depending on the observer. The magnitude of induction by the background color was modulated on average by 7.6% by chromaticity changes in the remote color fields. Chromaticity changes in the remote fields had virtually no inducing effect when they occurred without a change in background color. The spatial range of these chromatic interactions extended over at least 10 degrees from the fovea. They were established within the first few hundred milliseconds after the change of background color and depended only weakly on the number of inducing fields. These results may be interpreted as reflecting rapid chromatic interactions that support robustness of color vision under changing viewing conditions.
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