Cambridge Colour Test: reproducibility in normal trichromats.

This study evaluated reproducibility of the Trivector subtest of the Cambridge Colour Test. Data for normal trichromats were obtained in Brazil ($ N = 111 $N=111) at T0, six months (T1), and 12 months later (T2), and in the United Kingdom (${ N}={79}$N=79), with the test directly followed by a retest. Coefficients of repeatability-Bland-Altman indices-for Protan, Deutan, and Tritan vectors were similar for both datasets. Intraclass correlation coefficients (ICCs)-measures of reliability-were low or moderate for these relatively homogeneous datasets; for a heterogeneous dataset, comprising color-normal and abnormal observers, ICCs were 0.80-0.98, indicating the high discriminative accuracy of the Trivector subtest.

Effect of luminance on color perception of protanopes.

Small-field color-naming performance of two protanopes over a 4-log luminance range was impoverished in comparison with that of normal trichromats, and was more strongly affected by changes in luminance. At 200 cd/m2 responses to mid-spectral lights were dominated by 'yellow'; with lowering luminance, 'green' and 'red' were increasingly used. In the color spaces derived from these data the first two dimensions for trichromats are red-green and yellow-blue: those of the protanopes appear to be brightness and 'red-blue'. In the protanopes' color space the greater separation of stimuli at 0.2 cd/m2 suggests that with low luminance their color discrimination improves.

[The spherical theory of color perception: its verification by the methods of psychophysics and neurophysiology]. / Sfericheskaia teoriia vospriiatiia tsveta: proverka metodami psikhofiziki i neirofiziologii.

In the paper data of experimental verification of "spherical theory of perception" (E. N. Sokolov) are summed on the material of colour perception study. The results of psychophysical experiments with subjects having different forms of colour perception (normal trichromats, colour anomalies) and neurophysiological experiments on animals (carp) are considered within single psychophysiological system--spherical model of colour discrimination. Neuron-like elements of the model reflect the activity of light-sensitive cells of the visual system and at the same time reproduce some rules of subjective colours discrimination at the psychophysical level. Advantages of spherical model are considered allowing to analyze human individual colour functions in norm and pathology and giving the opportunity of strictly quantitative approach to description of neuronal mechanisms of colour vision. From the position of spherical model of colour discrimination neuronal structure of colour analyzer is discussed, which includes layers of photoreceptors, ++predetectors (colour-opponent and achromatic cells) and colour-selective detectors.

[Color perception in twins]. / Vospriiatie tsveta u bliznetsov.

The classical twin method was used to examine the genotype--phenotype relationship in color vision. Suprathreshold color differences were assessed by 5 pairs of monozygotic (MZ) and 3 pairs of dizygotic (DZ) twins. The control group included 3 unrelated normal trichromats, a non-twin sibling pair, and a previously diagnosed deuteranomal. Concordance rates were calculated by Spearman's correlation coefficients (rs) and Procrustean distances (gl) between the reconstructed color spaces for each related pair of observers. For 4 pairs of the MZ twins, the rs values were comparable to intraindividual variability in the control normal trichromat; they were significantly higher (0.94-0.97) than those for the DZ twins and siblings (0.72-0.82). The gl values for the MZ twins (0.008-0.029) were lower than for the DZ twins (0.073-0.079) and siblings (0.053). The high concordance between each pair of the MZ twins suggests that their shared photopigment genome constrains a contribution of possible individual variations in nongenetic factors to variability of their color spaces. Lower concordance rates in the DZ twins and siblings can be attributed to differences in the inherited arrays of photopigment genes. Contributions to intrapair variation in color spaces of twins from cognitive factors such as perceptual-cognitive color categorization and decision-process variability are discussed.

Color spaces of color-normal and color-abnormal observers reconstructed from response times and dissimilarity ratings.

With multidimensional scaling analysis, color spaces were reconstructed from reaction times (RTs) required to make same-different judgements of pairs of 15 equiluminant colors and from dissimilarity ratings between them. In addition to normal trichromats, observers with red-green color deficiency were tested. Two main purposes were served by this study: (1) to compare spatial representations of colors derived from discriminative RTs with those derived from dissimilarity measures and (2) to examine whether the task may selectively affect the dimension reflecting, in color-abnormal spaces, the deficient red-green mechanism. Contradicting our hypothesis of lower dimensionality of RT spaces, as compared with rating spaces, no consistent differences in solution dimensionality were found. However, configurations derived from the two measures diverged. The rating procedure yielded the most logical results for recovering color space. The RT configuration revealed contraction in the tritanopic direction, indicating longer color processing when the short-wavelength mechanism is involved, and in addition, for color-abnormal observers, clustering in the protanopic and deuteranopic directions, indicating even longer processing by the deficient red-green mechanism. This finding implies that RTs are suitable for detecting temporal differences in color processing but, for that very same reason, rather ill-suited for reconstructing color spaces.

Contrast discrimination and choice reaction times at near-threshold pedestals.

Choice reaction times (CRTs) to contrast differences were measured and compared with contrast increment thresholds obtained from concurrently measured psychometric functions at pedestal contrasts in the vicinity of detection threshold. Contrast discrimination functions had a classical dipper shape. The main finding was that CRTs were shorter at low pedestal contrasts but longer at higher pedestal contrasts compared to detection, reflecting the behaviour of increment thresholds. Even when equalized for response accuracy, CRTs varied with pedestal contrast in a similar manner to the contrast increment thresholds. The finding that CRTs and contrast increment thresholds depended on pedestal contrast in a similar manner suggests that both share a common origin. This common origin is proposed to lie in the variability of the sensory effect which determines the variability of the information accumulation process, which in turn affects the response criterion and contrast increment thresholds. At low pedestals, a decrease in variability lowers thresholds and results in a lower response criterion, thereby accelerating reaction times. At high pedestals, increasing signal-dependent noise inflates variability and thus raises thresholds and the response criterion, which results in slower CRTs.