The perceived color of a light varies with the background on which it is seen. In the present study, patterned backgrounds composed of two different chromaticities caused larger shifts in perceived color than did a uniform background at either chromaticity within the pattern. Cortical receptive-field organization, but not optical factors or known retinal neurons, can account for the color shifts from patterned backgrounds.

Chromatic induction from patterned backgrounds depends on the spatial as well as the chromatic aspects of the background light. Color appearance with patterned and uniform backgrounds was compared using chromaticities distinguished by only the S cones; all backgrounds were equivalent to equal-energy white in terms of L-cone and M-cone stimulation. The measurements showed larger shifts in color appearance with a patterned chromatic background than with a uniform background at any chromaticity within the pattern. The measurements also showed that inducing light within different spatial regions could cause opposite shifts in color appearance: inducing light near a test field shifted appearance toward the inducing chromaticity (assimilation), while the same light some distance from the test shifted appearance away from the inducing chromaticity (simultaneous contrast). The shifts in color appearance were accounted for by a neural receptive field with S-cone spatial antagonism.

Patterned backgrounds that selectively stimulate the S-cones cause conspicuous color shifts. These shifts are accounted for by an S-cone antagonistic (+S/-S) center-surround receptive field [Monnier, P., & Shevell, S. K. (2004). Chromatic induction from S-cone patterns. Vision Research, 44, 849-856]. The present study tested two additional implications of the S-cone receptive field for color shifts: (1) proportionality of the shifts with respect to S-cone contrast within the inducing pattern and (2) bandpass selectivity of the shifts with respect to the spatial frequency of the inducing pattern. Measurements showed that the magnitude of the color shift was linear with S-cone contrast and that the largest color shift was observed with inducing patterns at an intermediate spatial frequency. These results further support an S-cone spatially antagonistic receptive field as the neural substrate mediating the large color shifts from S-cone patterns.

We measured color-breakup thresholds for a simple field-sequential color stimulus while varying its luminance, contrast, and retinal velocity. Data analysis yielded an equation that predicts whether color breakup will be visible for specified viewing conditions. We compare this equation with an earlier version and discuss its uses and limitations.

Inducing patterns that selectively stimulate the S cones can induce large shifts in color appearance. For example, a "peach" test-ring presented within contiguous purple and non-contiguous lime inducing rings appears pink while the physically identical peach test-ring appears orange when presented within contiguous lime and non-contiguous purple inducing rings (Fig. 1c). These shifts have been accounted for by a neural substrate which predicts that chromatic assimilation and simultaneous contrast can operate synergistically to produce large shifts with these patterns [Monnier, P., & Shevell, S. K. (2004). Chromatic induction from S-cone patterns. Vision Research, 44, 849-856]. Here, induction was measured for test-rings that stimulated the S cones either more or less than did the inducing rings. According to standard definitions of induction, color shifts for test s-chromaticities either lower or higher than both inducing chromaticities should be attenuated compared to test-rings of intermediate S-cone stimulation. On the other hand, a previously proposed model of induction predicted independence of the color shifts with test-ring s-chromaticity. Consistent with standard definitions of induction, a reduction in the magnitude of the color shifts for test-ring chromaticities either lower or higher in S-cone excitation than the inducing chromaticities was observed. Additional measurements with patterns that have been shown to isolate assimilation and simultaneous contrast were conducted. For these patterns, expectations based on standard definitions of induction suggested that the magnitude of the color shifts should be monotonic with the S-cone stimulation of the test-ring, and the direction of the color shift should reverse for test-ring chromaticities either lower or higher than both inducing chromaticities compared to test-rings of intermediate chromaticity. In contrast, the previously proposed model of induction based on a receptive-field with S-cone spatial antagonism predicted the color shifts should be independent of the test-ring chromaticity (Monnier & Shevell, 2004). Color shifts were generally independent of the level of the test-ring chromaticity, supporting the S-cone antagonistic model of induction.

The quest for color head-and helmet-mounted displays has led some designers to consider the use of field-sequential color (FSC) because it offers higher resolution than conventional color displays in a compact package. Unfortunately, FSC displays exhibit color breakup sometimes, and the viewing conditions under which this occurs have not been established very well. We performed an experiment to determine color-breakup thresholds for a simple FSC stimulus as a function of stimulus luminance, contrast, and retinal velocity. We developed equations that describe the results and can be used to predict whether color breakup will be visible for specified viewing conditions.

We report on a cirrhotic patient who presented with an aortic valve endocarditis due to Pasteurella multocida. This disease entity is rare and we take this opportunity to review the 6 cases published to date.

This study investigated chromatic induction from inhomogeneous background patterns. Previous work showed that a background pattern detected by only S cones induced strong color shifts in a nearby test area (Monnier & Shevell, 2003). In that work, the S-cone patterns were composed with constant L- and M-cone stimulation over the entire background; in terms of L and M cones, therefore, the background was uniform. S-cone stimulation was varied over space to produce S-cone-isolated background patterns. These S-cone patterns, however, established spatial structure (the pattern) at both the receptoral level (S-cone stimulation) and the postreceptoral level (S/(L+M)). Here, these two levels of pattern representation were unconfounded to determine whether color shifts induced by S-cone patterns were due to spatial structure within an S-cone-specific neural pathway versus a pathway that combines responses from S cones and other cone types (e.g. S/(L+M)). The results showed that the induced color shifts were mediated by signals within a pathway that combines responses from multiple cone types. These results are consistent with a +s/-s spatially antagonistic neural receptive field, which is found in some neurons in V1 and V2.