EVALUATION OF COLOUR PERCEPTION STANDARD 3 OF ELECTRICAL PERSONNEL IN THE PERFORMANCE OF THEIR DUTIES.
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The paper analyses results after investigation of color perception in 520 children (264 boys and 256 girls), aged 3-5 years, by means of two simple tests: a "Pflüger-Trident Test" (Velhagen) and a "Simplified Test of Color Vision" (Fletcher). It is proved that in children of under school age color perception is already developed enough and can be investigated for detecting disturbances in color vision.
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PURPOSE: To investigate color vision in epilepsy patients treated with vigabatrin or carbamazepine monotherapy and to evaluate the association between vigabatrin-induced visual field defects and dyschromatopsia. DESIGN: Nonrandomized comparative trial. PARTICIPANTS: Thirty-two epilepsy patients treated with vigabatrin monotherapy, 18 patients treated with carbamazepine monotherapy, and 47 age-matched healthy controls were examined. MAIN OUTCOME MEASURES: Color vision was examined with Standard Pseudoisochromatic Plates 2 (SPP2) screening test, Farnsworth-Munsell 100 (FM 100) hue test, and Color Vision Meter 712 anomaloscope. RESULTS: Abnormal color perception was found in 32% of the epilepsy patients treated with vigabatrin monotherapy and 28% of the epilepsy patients treated with carbamazepine monotherapy. The total error score in the Farnsworth-Munsell 100 hue test was abnormally high in the vigabatrin monotherapy patients who had concentrically constricted visual fields and a statistically significant correlation was found between the temporal visual field extents and the age-adjusted Farnsworth-Munsell 100 total error score in vigabatrin monotherapy patients (R = .533, P = 0.003 in the right eye, R = .563, P = 0.001 in the left eye). Four of 31 (12%) vigabatrin monotherapy patients, and 1 of 18 (6%) carbamazepine monotherapy patients had a blue axis in Farnsworth-Munsell 100 hue test. In the anomaloscope, there were a few pathologic findings in both groups. In the SPP2 screening test, a few plates were not seen in both groups. CONCLUSIONS: Both examined antiepileptic drugs, vigabatrin and carbamazepine, cause acquired color vision defects. The abnormal color perception seems to be associated with constricted visual fields in the vigabatrin monotherapy patients. The duration of carbamazepine therapy correlates with high FM100 total error score. The best method for detecting dyschromatopsia in patients treated with vigabatrin or carbamazepine was the Farnsworth-Munsell 100 hue test. The SPP2 screening test does not seem to be useful in clinical practice.
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BACKGROUND: It has been reported that the differences in macular pigment between Asian and Caucasian eyes might give rise to different performance on the Farnsworth-Munsell 100 Hue test. However, the study did not appear to account adequately for the observation that differences were apparent only in older age groups. It was also acknowledged that other factors, like pupil size and crystalline lens colouration, could influence the result. METHOD: We investigated the performance of the Farnsworth-Munsell 100 Hue test, under standard conditions, by three groups with presumed different macular pigmentation and narrow age range. We also measured pupil size. RESULTS: The group with blue irides (presumed low macular pigmentation) performed significantly better on the colour vision task than the Asian group and the brown-eyed subjects as a whole (presumed higher macular pigmentation). In addition, the difference in pupil size between the blue-eyed group and brown-eyed groups bordered on significance. The difference in pupil size and consequential reduction in retinal illuminance account for a significant proportion of the difference in colour vision performance. In addition, a difference in both pupil size and Farnsworth-Munsell 100 Hue test performance was also observed between males and females that reinforced the importance of pupil size, and not just macular pigment, as a factor in colour vision performance difference between Asian and non-Asian eyes. CONCLUSION: It is concluded that pupil size, not just macular pigment, may have a significant influence on colour vision performance in a young, healthy population.
We tested whether motion and configural complexity affect perceived transparency. A series of five coherent chromatic transformations in color space was applied across a figure: translation, convergence, shear, divergence and rotation. The stimuli consisted of a bipartite or a checkerboard configuration (10 x 10 degrees), with a central static or moving overlay (5 x 5 degrees). Three different luminance conditions (the plane of chromatic transformation oriented toward higher, lower, or equal luminances) were also tested for each of three modulation depths. For each stimulus, the observer judged whether the overlay appeared transparent or not. The main results indicated an interaction between the type of chromatic transformation and stimulus motion and complexity. For example, convergences are judged to appear transparent significantly more often when motion is added for bipartite configurations, or when they are generated in a checkerboard configuration. Surprisingly, shears that have been reported to appear opaque, are more frequently reported to appear transparent with short vector lengths and when combined with motion. Other transformations are also affected by motion, although the effectiveness of figural complexity on transparency seems to depend on both the type of color shifts and the presence of motion. The results indicate that adding motion and stimulus complexity are not necessarily neutral with respect to the chromatic shifts evoking transparency. Thus, studies that have used motion to enhance transparency may yield different results about the color shifts supporting transparency perception from those that did not. The same might be supposed for stimulus complexity under some conditions.
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There are recurrent reports that Rayleigh matches are bimodally distributed in the colour-normal male population. Similar claims have been made for the distribution of the spectral locus of unique green. Moreover, a positive correlation has sometimes been reported between Rayleigh matches and unique green. Using a computer-controlled Maxwellian colorimeter and bias-free psychophysical methods, we measured both variables for 97 colour-normal male observers. We do not find a bimodal distribution either of Rayleight matches or of settings of unique green. Nor do we find any correlation between the two variables. However, we do observe a very significant relationship between the lightness of the subject's iris and the wavelength that he judges to be unique green.
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