We measured the regions in isoluminant color space over which observers perceive red, yellow, green, and blue and examined the extent to which the colors vary in perceived amount within these regions. We compared color scaling of various isoluminant stimuli by using large spots, which activate all cone types, to that with tiny spots in the central foveola, where S cones, and thus S opponent (S(...

The effects of glaucoma and diabetes on the sensitivities of the opponent and achromatic systems were investigated by measuring thresholds along theoretically defined axes in a three-dimensional color space. Thresholds were measured along two equiluminant chromatic axes and one achromatic axis in patients with diabetes or glaucoma and in glaucoma suspects. The results were compared with measure...

This is the cover letter for our paper entitled “A Tone Reproduction Operator for All Luminance Ranges Considering Human Color Perception”. This document explains the details of the proposed method, especially, the opponent color spectral sensitivities computed during the operation of the proposed method and the wavelength discrimination curves that correspond to the adapted retinal illuminance...

The two major theoretical accounts of color vision are those classified as the Young-Helmholtz and the Hering types of theories. For many years the former has been judged by most workers in the field to provide the simplest explanation of the way in which light stimuli give rise to color sensations. The advantages that appear to favor the Young-Helmholtz three-component hypothesis are two: it i...

The predominance of rivalrous targets is affected by surrounding context when stimuli rival in orientation, motion or color. This study investigated the influence of chromatic context on binocular color rivalry. The predominance of rivalrous chromatic targets was measured in various surrounding contexts. The first experiment showed that a chromatic surround's influence was stronger when the sur...

To investigate how rod signals influence hue perception and how this influence can be incorporated into opponent-color models, we measured the shift of unique-hue loci under dark-adapted conditions compared with cone-plateau conditions. Rod signals produced shifts of all spectral unique hues (blue, green, yellow) but in a pattern that was inconsistent with simple additive combinations of rod an...

We measured phase shifts between Long-wavelength cone (L-cone) and Middle-wavelength cone (M-cone) signals as well as sensitivity in the luminance pathway either following a cone-silent substitution of colored background or on a steady colored background. In background substitution, the phase shifts between L- and M-cone signals varied only slightly depending on the substituted color, whereas m...

The spatial structure of color cell receptive fields is controversial. Here, spots of light that selectively modulate one class of cones (L, M, or S, or loosely red, green, or blue) were flashed in and around the receptive fields of V-1 color cells to map the spatial structure of the cone inputs. The maps generated using these cone-isolating stimuli and an eye-position-corrected reverse correla...

Retinal specializations such as cone-photoreceptor opsin-expression gradients, as found in several vertebrate species, are intuitively considered detrimental to color vision. In mice, the majority of cones coexpress both "blue" and "green" opsin. The coexpression ratio changes along the dorsoventral axis, resulting in a "green"-dominant dorsal and a "blue"-dominant ventral retina. Here, we aske...