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Protanopes and deuteranopes do not accept the classical dichromatic matches when field size extends to 8 degrees visual angle. Their unique matches of spectral yellow to a mixture of red and green are then mediated by the photoreceptors of small-field dichromacy interacting with a photoreceptor with the spectral sensitivity of rhodopsin. Our data suggest that large-field trichromacy is a general feature of protanopia and deuteranopia.

The duration necessary to detect chromatic stimuli was measured for wavelengths between 463 and 620 nm. Stimuli were presented either in hue substitution (replacement of white by a chromatic stimulus of matched luminance) or as increments. Two observers viewed a 1 degrees 45' homogeneous white field. A trial consisted of replacement of the central 40' of the field by a chromatic stimulus. In substitution mode the white field was 2.4 cd/m2., the chromatic replacement was of matched luminance using heterochromatic flicker photometry (HFP). In increment mode, the white field was decreased to 1.2 cd/m2., the chromatic replacement remained at 2.4 cd/m2. In substitution mode, duration threshold varied from approximately 3--4 ms for the spectral extremes to 45--66 ms at 570 nm. Detected stimuli were always seen as a change in chromaticity. In increment mode, thresholds were in the 2--4 ms range with no dependence upon spectral composition. Detected stimuli were seen either as changes in chromaticity or brightness. A control experiment indicated that HFP did establish equivalent luminance for the hue substitution mode. We conclude that duration thresholds in substitution mode reveal chromatic processing channels; duration thresholds in increment mode are mediated by chromatic and/or achromatic processing channels.

Two-pulse discrimination thresholds determined for homochromatic pulses presented as luminance increments or decrements are invariant with wavelength. Wavelength does affect two-pulse temporal resolution if chromatic pulses are presented in hue substitution, matched in luminance (with flicker photometry) to an achromatic background field. For relatively long pulses, the wavelength effect resembles trichromatic saturation discrimination, with poorest temporal resolution at 570 nm. For shorter pulses, temporal resolution for hue substitution stimuli appears related to saturation discrimination under conditions of artificial tritanopia. Under conditions of hue substitution, short-wavelength pulses yield good temporal resolution.

We evaluated color matching in 39 observers with an autosomal dominant tritan defect. Eleven tritans were dichromats with 1 degrees field, and only two were dichromats with an 8 degrees field. Twenty-one of the tritan observers ahd normal blue-green equations with an 8 degrees field, indicating that autosomal dominant tritans have short-wavelength-sensitive cones. Some of the tritan observers showed a shifted blue-green equation, which was ascribed to rod activity.

The brightness of lights defined by heterochromatic flicker photometry as being of equal luminance was determined by direct comparison with a white standard. Stimuli included mixtures of white and colored lights. Eight different colorimetric purities were tested for each of eleven primaries. Adaptation to a known white was maintained. Resulting brightnesses were expressed in terms of the ratio of the amount of light required for a brightness match to the amount required for a flicker photometric match (B:F). B:F ratios varied with the primary, being largest for red and blue primaries. The variation of B:F ratio with colorimetric purity differed depending on the primary, although for any given dominant wavelength the highest-purity stimulus always had the largest B:F ratio. The data qualitatively exclude a number of simple models of brightness generation.

The spectral sensitivity of the visual photopigments, the interobserver variability in color judgments, and the spectral locus of unique yellow provide three major problems for accounts of X-chromosomal-linked anomalous trichromacy. According to the single-pigment hypothesis, the primary defect in anomalous trichromacy is a wavelength shift in the peak sensitivity of one of the three visual photopigments. We show that this shift results in reduction of the anomalous trichromat's r-g opponent chromatic channel. The distribution of response variability in Rayleigh equation match widths due to factors other than the spectral characteristics of the photopigments is similar in normal and anomalous trichromats. When normal and anomalous trichromats make hue estimations of sets of stimuli designed to contain similar chromatic information, their judgments show similar variability. Calculation of the r-g opponent chromatic channel can provide correct predictions of the spectral loci for unique yellow for anomalous trichromats.

Red-green color mixture equations were measured in 10 color-normal observers for fields of view varying from 30' to 10 degrees. The G/R mixture decreases continuously as field size is increased. The data are consistent with the interpretation that the cone visual photopigments decrease exponentially in effective optical density as the field size is increased.