CHROMATIC ROD VISION III. Duration of pre-stimulation varied

S tabell B. & S tabell U. Chromatic rod vision. III. Duration of pre-stimulation varied. Scand. J. Psychol ., 1972, 13 , 136–140.—The scotopic contrast hue was determined as a function of duration of pre-stimulation, together with the additive opponent hue. It is concluded that the red/blue ratio which has to be added to the additive opponent hue to produce the scotopic contrast hue, may change as a function of both wavelength and duration of pre-stimulation.     

ROD VISION AS CHROMATIC VISION

S tabell , B. Rod vision as chromatic vision. Scand. J. Psychol ., 1968, 9, 282–288.—It was found (I) that the smallest quantity of light of pre-stimula-tion which produces color upon test-stimulation, stands in unique relation to the intensity of the specific threshold, and (2) that the size of the pre-and test-stimulation fields may affect the duration of the after-image. The results are judged to indicate that pre-stimulation of cones creates the disposition for the color-related response, and that the color-related response is generated centrally to the photochemical systems of the receptors.     

TRANSITION FROM ROD TO CONE VISION:III. Successive contrast anew

S tabell , U. & S tabell , B. Transition from rod to cone vision. III. Successive contrast anew. Scand. J. Psychol ., 1969, 10 , 140–144—The relation between the specific threshold level and the upper limit of the scotopic contrast color was investigated. The achromatic interval between the scotopic and the photopic component increased when time in darkness increased, and when pre-stimulation was reduced as regards intensity, duration, or cone/rod ratio. The results are interpreted on the basis of the opponent theory of color vision.     

COLOR THRESHOLD MEASUREMENTS IN SCOTOPIC VISION: Test-stimulation varied

S tabell , U. & S tabell , B. Color threshold measurements in scotopic vision. II. Test-stimulation varied. Scand. J. Psychol ., 1968, 9, 129–132.—The color threshold curve generally coincides with the dark adaptation curve of the rods, irrespectively of test-stimulation variation, confirming the assumption that a threshold response of rods may initiate a color-related process. Variation of color threshold intensity is thus assumed to reflect variation of rod threshold intensity.     

Scotopic and photopic afterimages

Stabell, U. & Stabell, B. Scotopic and photopic afterimages. Scand. J. Psychol., 1973, 14, 210–212.MdashThe curves of photopic and scotopic afterimages were found to coincide, confirming the suggestion that disposition for scotopic contrast hue is controlled basically by the ratio of hue-related processes initiated upon chromatic prestimulation of cones, while the achromatic test-stimulation is a constant stimulus, regardless of test variables.     

CHROMATIC ROD VISION

STABELL, B. & STABELL, U. Chromatic rod vision. I. Wavelength of test-stimulation varied. Scand. J. Psychol. , 1971, 12, 175–178.–The ability to distinguish one type of radiation from another by its hue disappears in scotopic vision. Accordingly, scotopic hues are found to be invariant of variation of wavelength. It is concluded, on the basis of the Principle of Univariance, that hues may be triggered by light signals initiated in one type of receptor.     

COLOR THRESHOLD MEASUREMENTS IN SCOTOPIC VISION: Simultaneous color contrast

S tabell , U. & S tabell , B. Color threshold measurements in scotopic vision. III. Simultaneous color contrast. Scand J. Psychol ., 1968, 9, 133–137.—Color may be observed well below the break-point level of the dark adaptation curve, suggesting that the impulse pattern initiated in the rods may trigger a color-related response. Color is induced when the intensity of the inducing field reaches a certain level above the specific threshold, provided the stimulation of the test field is observable.     

Chromatic rod vision VII. Intensity of pre-stimulation varied

Stabell, B. & Stabell, U. Chromatic rod vision. VII. Intensity of pre-stimulation varied. Scand. J. Psychol., 1973, 14, 12–15.-Change in scotopic hue with variation of intensity of pre-stimulation was predicted on the basis of Hering's opponent theory of color, but the experimental results could not be adequately explained within the framework of the theory.     

Chromatic rod vision VIII. Simultaneous contrast

Stabell, U. & Stabell, B. Chromatic rod vision. VIII. Simultaneous contrast. Scand. J. Psychol., 1973, 14, 1619.-Compared with the curve of additive opponent hue, the curve of scotopic hue of simultaneous contrast was found to be displaced toward blue in the orange and green-yellow regions of inducing field. The results are explained on the assumptions that (a) change of disposition for scotopic hue reflects variation in ratio of primary hue-related processes of inducing field, and (b) the chromatic-related opponent processes, in a dark-adapted and chromatically neutral eye, are of equal magnitude within the photochromatic interval.     

Scotopic contrast hues displaced toward blue

Abstract.— Pre-stimulation with a neutral white light, in a dark-adapted state, produced a disposition for a scotopic hue of violet of about 463 nm. The observation may be explained on the basis of Helmholtz's theory of complementary negative afterimages, provided that (1) the assumption that neutral white is observed when the three types of cone receptors are activated to about the same degree, is rejected, and (2) the origin of the scotopic contrast hues is assumed to be located centrally to the photochemical systems of the receptors.     

DURATION OF SCOTOPIC CONTRAST HUES

STABELL, U. & STABELL, B. Duration of scotopic contrast hues. Scand. J. Psychol. , 1971, 12, 106–112.–It is generally accepted that following intense and prolonged bleaching, regeneration of cone pigments in man takes a few minutes to reach completion. The results show that the scotopic hue may remain visible for more than one hour. Hence, it is suggested that light signals and not bleaching signals produce the scotopic contrast hues.     

TRANSITION FROM ROD TO CONE VISION: II. Successive contrast

S tabell , B. & S tabell , U. Transition from rod to cone vision. II. Successive contrast. Scad J. Psychol., 1969, 10 137–139—Transition from chromatic rod to chromatic cone activity during dark adaptation is interpreted as a kind of color mixing.     

Scotopic contrast hues displaced toward red

Stabell, B. & Stabell, U. Scotopic contrast hues displaced toward red. Scand. J. Psychol., 1973, 14, 316–319.-The displacement of scotopic contrast hues toward red, contrary to predictions based on the opponent color theory of Hering, is explained on the assumption that the violet receptor system has a negligible sensitivity at the yellow cardinal point, while all the receptor systems are activated at the blue cardinal point.     

CHROMATIC ROD AND CONE ACTIVITIES AS A FUNCTION OF THE PHOTOCHROMATIC INTERVAL

S tabbll , B. & S tabell , U. Chromatic rod and cone activities as a function of the photochromatic interval. Scand. J. Psychol ., 1969, 10,215– 219.—The Sco topic contrast color dominated for longer periods and at higher intensities the larger the magnitude of the photochromatic interval, indicating that the relative responsiveness of the chromatic rod to the chromatic cone activity increases as a function of the photochromatic interval.     

Scaling of saturation and hue in the nonspectral region

The saturation of two nonspectral hues, magenta and violet, and the hue shift between red and blue through the nonspectral region were both scaled by two methods, equisection to produce a difference scale, ψ_D, and ratio judgments to produce a magnitude scale, ψ_M. The colored stimuli were viewed through apertures in a dark surround, with the luminance kept constant at one of three levels, 0.5, 2.5, and 12.6 cd/m². As previously found with saturation and hue shift between two adjacent primary hues in the spectral region, WD was linear with colorimetric purity for the saturation of magenta or violet and with the mixture ratio of red or blue for the hue shift, whereas ψ_M was a power function of colorimetric purity for the saturations and of the mixture ratio for the hue shift with exponents larger than unity in both cases. The present results were combined with previous results to give the change of parameters for saturation functions over the entire hue circle.     

TRANSITION FROM ROD TO CONE VISION I. Simultaneous contrast

S tabell , B. Transition from rod to cone vision. I. Simultaneous contrast. Scand. J. Psychol ., 1969, 10 , 61–64.—Above the specific threshold, color quality depended on the test filter, while at lower intensities the same color was observed irrespectively of the test filter used, confirming the assumption that colors within the photochromatic interval are triggered by rod activity. The lawful relation between rise of specific threshold and increase of rod sensitivity was not found under the condition of simultaneous contrast.     

Biological components of colour preference in infancy

Adult colour preference has been summarized quantitatively in terms of weights on the two fundamental neural processes that underlie early colour encoding: the S−(L+M) (‘blue–yellow’) and L−M (‘red–green’) cone‐opponent contrast channels ( Ling, Hurlbert & Robinson, 2006 ; Hurlbert & Ling, 2007 ). Here, we investigate whether colour preference in 4–5‐month‐olds may be analysed in the same way. We recorded infants’ eye‐movements in response to pairwise presentations of eight colour stimuli varying only in hue. Infants looked longest at reddish and shortest at greenish hues. Analyses revealed that the L−M and S−(L+M) contrast between stimulus colour and background explained around half of the variation in infant preference across the hue spectrum. Unlike adult colour preference patterns, there was no evidence for sex differences in the weights on either of the cone‐opponent contrast components. The findings provide a quantitative model of infant colour preference that summarizes variation in infant preference across hues.     

Infants are trichromats.

Two experiments were conducted to demonstrate that human infants 3 months of age perceive color in a normal, trichromatic manner. In the first experiment, the visual attention of 30 infants was monitored in a habituation-dishabituation paradigm that used spectral and white lights with brightness factors eliminated. Infants discriminated white from monochromatic light in a region of the spectrum (490–500 nm) where color-normal adults can but color-deficient adults cannot. In the second experiment which also used a habituation paradigm, eight infants showed good discrimination between hues in a region of the spectrum (560–580 nm) where color-deficient adults typically show no hue discrimination. Results from these studies of the neutral zone and hue discrimination evidence trichromatic vision in infancy and are discussed in the context of their several clinical, social, and intellectual implications.     

Hue shift of induced colour as a function of luminance relations

The hue of induced colour was studied as a function of surround/test field luminance ratio using a chromatic surround and an achromatic central test field. The hue of the test field was determined by means of colour naming methods. Three inducing colours were used: blue (Wr No. 47), green (Wr No. 58), and red (Wr No. 25). The number of subjects was 9–11 in the two experiments. The luminance ratio (ranging from 0.07 to 17.1) was varied by varying the luminance of the test field (Experiment 1) or of the surround (Experiment 2). For the blue surround the results show a hue shift in accordance with the Bezold-Brücke phenomenon. For the inducing colours green and red the induced colours are weak, and the hue shifts are more or less unsystematic though there are individual subjects showing a trend in the Bezold-Brücke direction. It is concluded that the hue shifts depend on the luminance relations rather than on the test field luminance.