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PubMed1992

Chromaticity and luminance as coding dimensions in visual search.

Visual search times were measured as a function of chromaticity and luminance differences between a target and distractor stimuli. Results showed that mean search time increased linearly with the number of distractors if the luminance difference between target and distractors was small but was roughly constant if the luminance difference was large. Similar results were previously found for chromaticity differences. With the number of distractor stimuli held constant, the mean search time decreased with increases in the difference between target and distractors, up to some critical difference. Further increases in target-distractor difference had little effect. Results were similar for targets defined by luminance and chromaticity. There was some advantage to combining luminance differences with chromaticity differences when the target was dimmer than the distractors. Generally there was no advantage for combining a chromaticity difference with a luminance difference when the target was brighter than the distractors.

Adult↗
PubMed1977

Analysis of chromatic-adaptation effect by a linkage model.

Hunt suggested that an adaptation-dependent linkage in the visual pathway from the retina to the brain can explain the variation of saturation produced by change of adapting luminance. If variation of saturation is caused by change of linkage, this change must also be involved in chromatic adaptation to light sources that have different chromaticities. By considering the effective adaptation levels of receptors, the model is extended and formulated for application to prediction of chromatic adaptation. It is tested by use of experimental results for chromatic adaptation obtained by Burnham et al. Suitable selection of parameters that specify the state of linkage produces good predictions of the effects of chromatic adaptation.

Adaptation, Ocular↗
PubMed1983

Relationship between chromatic induction and spatial variables: an integrated explanation in terms of element-contribution function.

Chromatic induction as a function of separation and as a function of area was determined by a hue-cancellation procedure. Both functions obtained were expressed by exponential functions with similar exponential coefficients. This led to the derivation of an element-contribution function, based on a linear summation model, that could explain both the relationship between chromatic induction and separation and that between chromatic induction and area. The effects of separation and area on chromatic induction could readily be determined in terms of an element-contribution function. In addition, the induction area that is due to a blue inducing stimulus was larger than those that are due to the other inducing stimuli, suggesting that the summation area of the blue response was larger than those of the other chromatic responses.

Adult↗
PubMed1983

Spatiotemporal variation of chromatic and achromatic contrast thresholds.

Moving the retinal image of a sinusoidal grating at a constant velocity (compensated for eye movements) provides controlled spatial and temporal frequencies at every point in the stimulus field. Using this controlled-velocity technique, we have measured the detection threshold for isoluminance, red/green gratings as a function of their spatial and temporal frequencies. The chromatic contrast-threshold surface obtained in this way is analogous to the achromatic contrast-threshold surface measured previously, but the results are quite different. For very low temporal frequencies (below 0.2 Hz), the chromatic sensitivity decreases steadily with decreasing temporal frequency. Below 0.01 Hz, chromatic patterns disappear completely even at maximum contrast (although achromatic or homochromatic patterns do not). In the region above 0.2 Hz, both achromatic and chromatic thresholds can be explained by the same receptive-field-like model. When the center and the surround components of this model are additively combined, they form the chromatic threshold surface; when the sign of either component is reversed, they form the achromatic one.

Color Perception↗
PubMed1993

Physiological mechanisms underlying psychophysical sensitivity to combined luminance and chromatic modulation.

If psychophysical detection thresholds are plotted in a middle-wavelength-sensitive (M) and long-wavelength-sensitive (L) cone coordinate system, the shape of the contour can be used to infer underlying detection mechanisms. We measured responses of macaque ganglion cells to combine chromatic and luminance modulation and expressed our results in such an M,L-cone space. Our aim was to test whether, with the use of this space, readily separable luminance and chromatic psychophysical mechanisms might be expected from physiological data. For parvocellular pathway cells, detection contours approximated elongated ellipses with maximum responsivity to chromatic modulation. The degree of elongation decreased as temporal frequency increased. Responses could be well described by linear subtraction of M- and L-cone signals, with a phase delay of 1-3 deg/Hz. For cells of the magnocellular pathway, detection contours were more complex. Orientation was variable between cells and temporal frequency dependent, and a frequency-doubled component was evoked by chromatic modulation. In relation to psychophysical detection thresholds plotted in such a space, the properties of parvocellular-pathway cells were sufficiently linear and homogeneous to make it plausible that this pathway might form the substrate for a linear chromatic mechanism. The properties of magnocellular-pathway cells, however, indicate that, insofar as a psychophysical luminance mechanism is based on their activity, its signature in the M,L-cone contrast space would be more difficult to identify.

Animals↗
PubMed1999

Global motion cues and the chromatic system.

The capacity of the isolated chromatic system to perceive global motion was tested in a 40-deg visual field by use of random-dot kinematograms. The method of equivalent cone contrasts was used to directly compare the chromatic and the achromatic systems. The minimum number of dots necessary to correctly identify the motion direction was on the order of 20% for the isochromatic conditions, whereas thresholds were rarely obtained in the chromatic conditions. For both the isochromatic and the chromatic conditions, the central visual field was the most sensitive area, whereas the periphery was slightly less sensitive. This study suggests that the chromatic system does not efficiently integrate local motion cues to generate a global motion percept.

Analysis of Variance↗
PubMed2004

Color constancy through inverse-intensity chromaticity space.

Existing color constancy methods cannot handle both uniformly colored surfaces and highly textured surfaces in a single integrated framework. Statistics-based methods require many surface colors and become error prone when there are only a few surface colors. In contrast, dichromatic-based methods can successfully handle uniformly colored surfaces but cannot be applied to highly textured surfaces, since they require precise color segmentation. We present a single integrated method to estimate illumination chromaticity from single-colored and multicolored surfaces. Unlike existing dichromatic-based methods, the proposed method requires only rough highlight regions without segmenting the colors inside them. We show that, by analyzing highlights, a direct correlation between illumination chromaticity and image chromaticity can be obtained. This correlation is clearly described in "inverse-intensity chromaticity space," a novel two-dimensional space that we introduce. In addition, when Hough transform and histogram analysis is utilized in this space, illumination chromaticity can be estimated robustly, even for a highly textured surface.

Journal Article↗
PubMed2005

Senescence of spatial chromatic contrast sensitivity. I. Detection under conditions controlling for optical factors.

Chromatic contrast thresholds for spatially varying patterns of various spatial frequencies (0.5, 1, 2, and 4 cycles per degree) were measured for ten older (65-77 yr of age) and ten younger (18-30 yr of age) observers. The stimuli were Gabor patches modulated along S-varying or (L - M)-varying chromatic axes. Thresholds were determined for two sets of stimuli. For one set of stimuli, the mean chromaticity and luminance were equated at the cornea for all observers. The second set of stimuli was corrected for ocular media density differences to equate stimulation of each of the three cone types at the retina for each individual. Chromatic contrast thresholds were higher for older observers for all stimuli tested. The magnitude of this difference showed little dependence on spatial frequency. When stimuli were equated at the cornea, this difference was greater for S-varying stimuli. When stimuli were equated at the retina, the age-related difference in thresholds for S-varying stimuli was reduced. Both optical and neural factors contribute to these age-related losses in spatial chromatic contrast sensitivity.

Adolescent↗
PubMed1987

Temporal modulation sensitivity and pulse-detection thresholds for chromatic and luminance perturbations.

We studied temporal processing of chromatic and luminance perturbations of a 600-nm field, measuring both modulation sensitivity (sinusoidal frequencies from 0.25 to 40 Hz) and pulse-detection thresholds (pulse durations from 5 to 2560 msec) for mean luminances of 0.9 to 900 Td and field sizes of 0.5 degrees to 8 degrees. Chromatic stimuli were produced by antiphase modulation of lights matched by heterochromatic flicker photometry. Both mean luminance and field size affected sensitivity, and the magnitude of field-size effects increased with mean luminance. We derived both luminance and chromatic impulse response functions for each set of experimental conditions, using the modulation-sensitivity data. At high mean luminances and large field sizes the chromatic impulse response functions are complex, suggesting contributions from both chromatic and luminance mechanisms. Pulse-detection data were fitted by a peak detector model based on these impulse response functions.

Color↗
PubMed1990

Luminance and chromatic modulation sensitivity of macaque ganglion cells and human observers.

We measured the sensitivity of macaque ganglion cells to luminance and chromatic sinusoidal modulation. Phasic ganglion cells of the magnocellular pathway (M-pathway) were the more sensitive to luminance modulation, and tonic ganglion cells of the parvocellular pathway (P-pathway) were more sensitive to chromatic modulation. With decreasing retinal illuminance, phasic ganglion cells' temporal sensitivity to luminance modulation changed in a manner that paralleled psychophysical data. The same was true for tonic cells and chromatic modulation. Taken together, the data suggest strongly that the cells of the M-pathway form the physiological substrate for detection of luminance modulation and the cells of the P-pathway the substrate for detection of chromatic modulation. However, at high light levels, intrusion of a so-called luminance mechanism near 10 Hz in psychophysical detection of chromatic modulation is probably due to responses in the M-pathway, arising primarily from a nonlinearity of cone summation. Both phasic and tonic ganglion cells responded to frequencies higher than can be psychophysically detected. This suggests that central mechanisms, acting as low-pass filters, modify these cells' signals, though the corner frequency is lower for the P-pathway than for the M-pathway. For both cell types, the response phase at different frequencies was consistent with the cells' description as linear filters with a fixed time delay.

Animals↗
PubMed1992

Sensitivity of macaque retinal ganglion cells and human observers to combined luminance and chromatic temporal modulation.

We measured the sensitivity of macaque retinal ganglion cells and human subjects to luminance and chromatic modulation and to two combined conditions as a function of temporal frequency. For both physiological and psychophysical data, we compared the sensitivities to luminance and chromatic modulation with the sensitivities in the combined conditions, using an additivity measure. When the physiological and the psychophysical data were taken together, the results suggested that under the combined conditions psychophysical sensitivity was the envelope of independent achromatic and chromatic mechanisms with physiological substrates in the magnocellular and the parvocellular pathways, respectively. In the combined conditions tested, sensitivity appeared to be set by a chromatic channel below 3 Hz and an achromatic channel above this frequency. This hypothesis was supported by a comparison of detection sensitivities with discrimination thresholds for the presence of chromatic alternation.

Adolescent↗
PubMed1991

Purely chromatic perception of motion in depth: two eyes as sensitive as one.

Motion hyperacuity (phase) thresholds were measured for both lateral and stereoscopic oscillatory motion in both luminance and equiluminant red/green gratings of 2 cycles per degree. Thresholds for lateral chromatic motion did not exhibit the inhibitory fall-off at low temporal frequencies that was found for luminance motion. Phase thresholds for purely chromatic motion were substantially higher than those for luminance gratings, in proportion to the ratio of cone signal modulation, but they could be predicted from the corresponding contrast sensitivities for both types of stimulus. Stereomovement thresholds in luminance gratings showed the stereomovement suppression effect relative to monocular motion sensitivity previously reported for line stimuli, but purely chromatic gratings did not. Together with the lack of an inhibitory fall-off, these results imply that chromatic and luminance motion are processed by different neural pathways, and that the chrominance pathway is capable of supporting a strong percept of stereoscopic motion from purely chromatic gratings.

Attention↗
PubMed1989

[Theoretical patterns of the panel D-15 test in congenital red-green dichromats as a function of the chromaticity coordinate of the convergence points].

In order to determine whether or not the patterns of the panel D-15 test for congenital red-green dichromats change when the convergence point is changed, a simulation experiment was attempted assuming that dichromats arrange the color caps in the order of the slope of the line between the chromaticity coordinates of the color cap and the convergence point. For this procedure, chromaticity coordinates of the color cap were calculated using both the spectral distribution of standard illuminant C and the daylight fluorescent lamp (Toshiba-EDL). For this prediction, the chromaticity coordinates of the convergence points were changed according to y = 1-x. The results show several different patterns for both protanopia and deuteranopia under both illuminants. The range of the x chromaticity coordinates common to both illuminants was 0.6868 to 0.8552 when the protanopic patterns were obtained, while the range of the x chromaticity coordinates common to both illuminants for deuteranopic patterns was 1.0878 to infinity and minus infinity to -1.8153. As a result, it was suggested that the patterns of the panel D-15 test for red-green dichromats change according to the convergence points. Therefore, it was considered that this test cannot be used as a dependable measurement for color discrimination ability in cases showing dichromatic patterns.

Color Perception↗
PubMed1994

Effects of colour adaptation and stimulus size on the detection of chromatic deviations from achromatic as a function of eccentricity in man.

By using constant size and M-scaled stimuli (the stimulus size was magnified towards the visual field periphery in inverse proportion to the lowest local sampling density of the human retina) we measured the thresholds for perceiving the complementary colours of blue, green and red (i.e. yellow, purple or blue-green) under chromatic adaptation at the eccentricities of 0-15 degrees in the nasal visual field. The CIE 1931 (x, y) chromaticity coordinates corresponding to complementary hue perception were subtracted from the chromaticity coordinates of achromatic threshold. The difference was found to be constant irrespective of stimulus size and eccentricity. This means that the perception of chromatic deviation from achromatic under chromatic adaptation is independent of stimulus size and eccentricity.

Adaptation, Ocular↗
PubMed1995

Different uses of chromatic signals in patients with congenital and acquired colour vision deficiencies.

Chromatic signals can be used to generate perceived colour and also to detect spatially structured objects defined only by chromatic differences. These two attributes have previously been investigated in dichromats and cerebral achromatopsic patients using a new colour vision test developed at City University that makes possible the isolation of pure chromatic signals (Barbur et al. Proc. R. Soc. London B 258, 327-334, 1994). We have investigated acquired colour vision changes in a 69-year-old patient, after conventional colour vision tests gave ambiguous results. His ability to detect an object using chromatic signals was impaired more than his ability to detect a colour change, and this impairment was greater in the right eye than in the left eye. This dissociation suggests parallel pathways may be involved in the two processes of coding chromatic signals. Recent neurological testing on the same patient has indicated the onset of multiple sclerosis. Our much earlier finding based on colour vision testing may therefore have useful diagnostic implications.

Aged↗
PubMed1995

Influence of the luminance signal and red-green and yellow-blue opponent chromatic signals in figural-stimuli stereograms.

The influence of color signals on stereopsis has been studied using figural-stimuli stereograms with variations introduced according to the opponent chromatic channels (red-green and yellow-blue), derived from Boynton's color-vision model. We used wallpaper stereograms, which enable the rank-order disparity ranges of the chromatic and luminance signals to be compared with the rank-order disparity range of proximity, a particular spatial configuration of the stereogram in which there are no variations in chromaticity and/or luminance. The results indicate that both chromatic signals contribute to stereopsis as does the luminance signal, contradicting the model of Hubel and Livingstone. The results also show there are no clear dependencies upon the kind of signal processed, as luminance and chromatic variations are processed with the same efficiency.

Color Perception↗
PubMed2001

Occupational cancer genetics: infrequent ras oncogenes point mutations in lung cancer samples from chromate workers.

BACKGROUND: Chromium carcinogenicity and mutagenicity are no longer disputed. However, although chromium has various genetic effects that induce cancer, its mechanism of inducing lung cancer in humans is still not fully understood. p53, a tumor suppressor gene, was found to be infrequently mutated in samples of lung cancer in workers with long occupational exposure to chromium, suggesting other cancer-related genes to be targeted in such tumors. METHODS: To assess the contribution of the ras oncogenes in the pathogenesis of chromate-related lung cancer, we studied point mutations at the critical positions of codons 12, 13, and 61 of the Ha-ras and Ki-ras oncogenes in 38 lung cancer samples derived from Japanese patients who worked in the chromate industry for long periods. We used both radioactive isotope and non-radioisotope PCR-SSCP techniques. RESULTS: The results of this study demonstrated that activation of ras genes due to point mutations in chromate-related lung cancer is a rare event. CONCLUSIONS: Ras oncogenes activated by point mutations do not have a major role in the process of tumorigenesis of chromate-related lung cancer.

Adult↗
PubMed2003

Microscopic analysis of chromium accumulation in the bronchi and lung of chromate workers.

BACKGROUND: It is known that chromium is an inhaled carcinogen and an important risk factor in the development of lung carcinoma. METHODS: The authors used a microscopic X-ray fluorescence analyzer with transmitted X-ray mapping imaging (Horiba, Kyoto, Japan) to measure the accumulation of chromium in 10 resected lung tissue specimens and 90 biopsy specimens from chromate workers. RESULTS: The maximum chromium accumulation (mean +/- standard deviation) in 10 resected lung tissue specimens was 197 +/- 238 counts per second (cps)/mili ampere (mA) (range, 4-649 cps/mA). Chromium accumulation was scattered in six tissue specimens and diffuse in one specimen. Chromium accumulation in the proximal bronchi was less than in the bronchioles or subpleural regions of the lung. Chromium accumulation was detectable in 63 (70%) of 90 biopsy specimens, and the mean accumulation was 6.5 +/- 9.2 cps/mA (range, 0-46.5 cps/mA). Chromium detected in bronchial tissue specimens was deposited in the bronchial stroma but not in the epithelium. The maximum chromium accumulations in dysplasic (n = 3), squamous metaplastic (n = 10), and normal bronchial epithelia (n = 9) in chromate workers and in normal bronchial epithelia (n = 3) in non-chromate workers were 20.2 +/- 5.4, 18.3 +/- 12.2, 13.2 +/- 13.4, and 3.0 +/- 1.8 cps/mA, respectively. The amount of chromium accumulation significantly increased according to the progression of malignant change of the bronchial epithelium (P = 0.003). CONCLUSIONS: Previous studies found that lung carcinoma with chromate exposure exhibited a variety of genetic abnormalities. Considering genetic aberrations and chromium accumulation in these premalignant lesions is useful for elucidating the process of carcinogenesis in chromium-induced lung carcinoma.

Adult↗