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PubMed1988

Color perception under chromatic adaptation: red/green equilibria with adapted short-wavelength-sensitive cones.

Chromatic adaptation can dramatically alter the color appearance of a light. The specific effect of adapting short-wavelength-sensitive (SWS) cones is examined by using two adapting wavelengths that lie on a tritanopic confusion line. The change in color appearance caused by signals from adapted SWS cones is isolated by restricting the wavelengths of the test light to 550 nm or longer. Thus the test negligibly stimulates SWS cones, so their sensitivity does not affect the test's appearance. The results show that adapted SWS cones contribute redness to the appearance of a superimposed test light, while not affecting sensitivity of MWS and LWS cones. Quantitatively, the redness from SWS cones illuminated by a large adapting field approaches physical admixture of test and adapting lights. This is very different from an adapting field that stimulates only MWS and LWS cones which, due to a postreceptoral process, contributes much less redness to a small superimposed test than expected from admixture. The difference between the adapted SWS-cone and the adapted MWS/LWS-cone contributions to the color of a small test explains a surprising result: a bluish-green (491 nm) adapting field contributes redness to a superimposed test light.

Adaptation, Ocular↗
PubMed1990

[Early diagnosis of congenital disorders of color vision with the Velhagen "Pflügerhaken Color Charts for evaluating color perception" in 3,375 preschool children].

In three series of examinations, 3375 male preschool-age children and 93 adult normal trichromates were tested using the Velhagen Pflügerhaken charts. The authors recommend modifying the evaluation of the results slightly by introducing a "doubteful" category for children who make one mistake or who show hesitation and lack of assurance in interpreting the charts. Using this modified form of assessment, diagnoses of "probably achromatopic" and "doubtful" were made in 7.16% and 2.13% respectively of 1689 preschool-age boys. The failure rate during the test and the duration of the examination were age-dependent, and declined with increasing age from 4.15% to 0.45% and from 1.18 min to 0.59 min, respectively. Most mistakes were made with charts nos. 9, 3, and 5. The results of tests with Pflügerhaken charts are fully comparable with those of other internationally used tests for adults. They can be recommended for screening preschool-age children.

Adult↗
PubMed1988

[The effect of combined iodine treatment in Bad Hall on the color perception of patients].

After taking a cure with iodine treatments in Bad Hall (Upper Austria), patients with eye diseases repeatedly report improvements in their color vision. They state that colors are once again "more saturated, richer, and more distinct." These statements were checked using the Farnsworth Panel D-15 dicotomous test and the Lanthony desaturated 15 Hue test. The analysis of the results showed that there is indeed a statistically significant improvement in color vision after the cure. The spontaneous observations of the patients were therefore confirmed by the study.

Adult↗
PubMedDate not supplied

[Contancy of color perception in the grey toad].

Under the conditions of behavioural experiment capacity of grey toads for constant perception of an object colour was studied. It is shown that irrespective of the spectral composition of light source toad males are able to recomgnize blue colorations among the other ones (green and grey of various gradations).

Animals↗
PubMed1987

[Visual evoked potentials following double-pattern stimulation with pseudo-color perception].

We examined in which form an additional structural stimulus in the white checks influenced the visual evoked potential of a checkerboard reversal induced response. A pattern of vertical bars was introduced with a short delay to the checkerboard reversal. The purpose of these experiments was to find out about the discrimination threshold of the occipital cortex for timely spaced stimuli. The double stimulus was separated from the next change minimally for 800 ms. With this arrangement we avoided "steady states", which are shown by repetitive interstimulus intervals of less than 200 ms. Nine normal volunteers between 22 to 28 years of age were measured. We found a typical waveform after the P 100 potential consisting of a positive peak followed by a negative long-lasting baseline elevation. Only separations of more than 60 ms yielded this configuration. Interstimulus times of less than 60 ms resulted in refractory effects on the visual evoked response. All the subjects reported colour or brightness changes of the additional bars. These pseudo colours were very probably due to the Prevost-Fechner-Benham-Effect which is common with repetitive white and black pattern changes. Our pseudo colours showed remarkable differences to the classical designs which has led us to the conclusion that colour perception on TV monitors is influenced so far by unpredictable flicker factors.

Adult↗
PubMed1991

Two carriers for motion perception: color and luminance.

Starting with the experiments of Ramachandran and Gregory (Nature, 275, 55-56, 1978), several psychophysical studies in apparent motion (AM) have established that the perception of motion is significantly impaired at equiluminance. Still debated, however, is whether color alone can resolve ambiguities in AM. We report here on several psychophysical experiments, the quantitative results of which indicate that color does play a substantial role in AM. These findings seem to support recently proposed neurophysiological frameworks according to which there exist significant interactions among the neuronal pathways mediating the perception of basic visual attributes such as color, motion, form and depth.

Color Perception↗
PubMedDate not supplied

[Constancy of color perception in the gray toad (Bufo bufo L.)].

Colour vision and constancy of colour perception in Bufo bufo L, were examined by means of unconditioned reaction of choosing moving and stationary models of females by males during breeding season. The males chose blue and dark blue models. Control of the choice of blue models presented in pairs with models of different shades of grey proves the existence of colour vision in Bufo bufo L. The choice of blue models has been observed under significantly varying conditions: both with artificial illumination and in sunlight. This attests the capacity of toads for constant colour perception. When a model was presented against a saturated red background, colour contrast was observed: under such conditions the toads chose the grey models which evoked no reactions when presented against white background.

Animals↗
PubMedDate not supplied

[Work of the human visual system. III. Color perception space].

In the previous parts of this work the author presented thet expression for percieved colour: Ei=k1n(ai/ao) where k -- is the coefficient of proportionality which have dimension of sensation and ai, ao -- are the light actions in some retinal point and in the extreme periphery correspondingly. Here the author describes some consequences from this expression and gives a new conception about the space of colour sensations.

Color Perception↗
PubMed1990

[Changes in color perception during the use of the Vacumcolor 50% tinted glasses in normal trichromatic individuals].

The authors assessed the spectral absorption of coloured glasses Vacumcolor 50% and found differences between different pairs of glasses which attained in the red areas as much as 17%. They also examined changes of the colour sense in a group of normal trichromats when using these coloured glasses. They found that these glasses alter the colour sense in the direction of deuteranomaly and cause deterioration of colour asthenopia.

Adult↗
PubMed1977

[Importance, especially in aeronautics, of color perception tests under dynamic conditions. Study of a suitable experimental apparatus].

Following a review of the most recent opinion on the physiology of colour vision, a device for examining it in dynamic, i.e. real-life conditions is described. The apparatus consist of two projectors which flash two absolutely identical pictures on to the screen, one of them is upside down. It appears at fixed but adjustable intervals so that the exposure time of the intelligible image can be varied. Subjects were also controlled with Ishihara charts and Nägel anomaloscope. The results are compared and point to the higher sensitivity of the dynamic test to even slight degrees of dyschromatopsia.

Color Perception Tests↗
PubMedDate not supplied

[The spherical theory of color perception: its verification by the methods of psychophysics and neurophysiology].

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.

Animals↗
PubMed1992

The dermo-optical perception of color as an information source for blind travelers.

Dermo-optical color perception refers to a person's ability to distinguish color surfaces through "skin perception" without the use of sight. The aims of this study were (1) to assess prior research findings which apparently demonstrated the existence of dermo-optical color perception and (2) to explore the possibilities of using color to indicate reference points for blind travellers. Three experiments were conducted with 20 congenitally blind subjects and a sighted blindfolded control group matched on age, sex, and education. In Exp. 1 on a discrimination task subjects were asked if two boards were of the same color and on a pairing task were asked to match a colored board with one among a set of three boards having the same color. In Exp. 2 the discrimination task was identical to that in Exp. 1, but instead of using boards perceived through haptic exploration, we used colored cubicles in which the whole body would be exposed to the color. In Exp. 3 subjects were asked to walk along the corridor of a labyrinthine set-up and to identify any changes of color they could perceive. The experiments were designed to provide measures of reliability of subjects' responses. Analysis showed little or no support for the ability to perceive color by dermo-optical means. The comparisons of the blind and the sighted control groups were nonsignificant. On the basis of our findings, the use of color to help blind travellers has to be rejected. The paper concludes with a discussion suggesting reasons for the contradictory results emerging from studies on dermo-optical color perception.

Adolescent↗
PubMed1989

Influence of achromatic surrounds on categorical perception of surface colors.

Color samples selected from the OSA Uniform Color Scales set were seen isolated in a dark field, illuminated by hidden projectors. These appeared as self-luminous aperture colors when thus isolated. We employed a categorical color-naming procedure to assess color appearance. Achromatic surrounds of 33 min width, if adjacent to samples subtending about 2.2 deg, were sufficient to render normal categorical surface-color perception. As the size of surrounds decreased, color naming shifted from that normally observed in the surface-color mode to that appropriate to the aperture-color mode. For isolated samples, brown was almost never seen, being most often replaced by orange; a white border less than one-sixtieth the width of the color samples was sufficient to restore its perception in an otherwise dark field. The reflectance of the surround and the gap between test and surround stimuli were also examined and found to be important factors in surface color perception, whereas the overall luminance level was not.

Adult↗
PubMedDate not supplied

[Perception of color and volumetric shape of objects].

The problem of recognition of coloration of volume objects, illuminated simultaneously with bright point ans weak diffuse sources (having arbirary and previously unknown spectra) is considered. A mathematical model, in which a process of recognition of coloration is accompanied by determining orientations of surface elements relatively the point source is described. The information on orientation allows in many cases to calculate the volume shape of objects of the external world form their monocular ""retinal"" image.

Color Perception↗
PubMed1992

Cortical area V4 and its role in the perception of color.

The color and lightness vision of three monkeys with bilateral removal of cortical area V4 and three unoperated controls were tested by measuring their ability to discriminate between two rows of colored or gray stimuli. In one row, the stimuli were ordered in terms of either chromaticity or luminance, whereas in the other row they were disordered. Their ability to select the odd-one-out in an array of colors or grays and to select the colored patch from an array of achromatic grays was also assessed. Unlike an achromatopsic patient tested previously in an identical fashion, monkeys with V4 lesions performed indistinguishably from controls in the oddity test. The animals lacking V4 were slightly impaired at discriminating between ordered and disordered arrays of colors or grays, but the color impairment was no more severe than the impairment with grays. These deficits were readily accounted for in terms of the conspicuous deficits in pattern discrimination apparent in a nine-choice pattern oddity task. The results do not support the view that cortical area V4 in the monkey is the homolog of the cortical "color center" in humans, located in the lingual and fusiform gyri and damage to which leads to the clinical syndrome of cerebral achromatopsia, unless it is the additional damage to underlying white matter that leads to the severe color disorder in patients.

Animals↗