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.     

Rod involvement in peripheral color processing

Abstract.— It has previously been suggested that rods act as blue receptors in peripheral color vision. Two experiments examining this issue were conducted. Experiment 1 investigated the perceived hue of a test light presented at a luminance level above chromatic threshold. At 8° in the periphery, the 500 nm test light was perceived as more blue under conditions of dark adaptation than after light adaptation. Similar differences were not found for foveal presentation. The increased blue in the periphery after dark adaptation was attributed to a rod contribution. In Experiment 2 an attempt was made to mix a rod contribution obtained with a 470 nm light below chromatic threshold, with a cone color obtained from a 670 nm light presented above chromatic threshold. No evidence was obtained to support the idea that a blue produced by rods stimulated below chromatic threshold could mix with a red produced by cones stimulated above chromatic threshold. The results are discussed in terms of a rod contribution to hue which is dependent on the luminance level of short wavelength stimulation.     

FACILITATION OF CHROMATIC CONE ACTIVITY BY ROD ACTIVITY

STABELL, U. & STABELL, B. Facilitation of chromatic cone activity by rod activity. II. Variation of chromatic-related cone activity. Scand. J. Psychol. , 1971, 12, 168–174.–At the cone-rod break of the dark adaptation curve, the specific threshold was found to drop to lower intensity levels, while the threshold curves of fovea proceeded in one step only, confirming the suggestion that rods may facilitate chromatic-related cone activity.     

The fluttering-heart illusion: a new hypothesis

The fluttering-heart illusion is a perceived lagging behind of a colour target on a background of a different colour when the two are oscillated together. It has been proposed that the illusion is caused by a differential in the perceptual latencies of different colours (Helmholtz 1867/1962), a differential in rod-cone latencies (von Kries 1896) and rod-cone interactions (von Grünau 1975, 1976 Vision Research 15 431-436, 437-440; 16 397-401; see list of references there). The purpose of this experiment was to assess the hypothesis that the fluttering-heart illusion is caused by a differential in the perceived velocities of chromatic and achromatic motion. To evaluate this hypothesis, we tested observers possessing normal colour vision and deuteranopes. The perceived delay of a chromatic target relative to an achromatic target was measured as a function of background cone contrast and target colour. For observers with normal colour vision, the perceived delay of the chromatic target is greater in the L-S than the L-M testing conditions. The reverse is observed in deuteranope observers. We suggest that this is caused by the absence of an L-M opponent mechanism contributing to chromatic motion in deuteranopes. Greater background cone contrasts tended to yield smaller perceived delays in both normal and deuteranope observers, indicating that greater chromatic modulation decreases the perceived delay of the colour target. These results support the hypothesis that the fluttering-heart illusion can be explained by a differential in the perceived velocities of chromatic and achromatic motion.     

RODS AS COLOR RECEPTORS IN PHOTOPIC VISION

Comparing a foveal and an extra-foveal field during dark adaptation, transition from chromatic to achromatic vision at intensity levels above the cone plateau started around the break of the dark adaptation curve. Pre-stimulating the two fields in a dark-adapted state with deep red, and test-stimulating when returning sensitivity had reached absolute threshold of the dark-adapted eye, with green filters at intensities above the specific threshold, the fields matched as to hue and saturation. It appears that rod and cone activities are integrated and function as a synchronized unit during the initial recovery phase of dark adaptation.     

Comparison of scotopic sensitivity in diurnal (Anas platyrhynchos) and crepuscular (Dendrocygna autumnalis) ducks.

Scotopic visual adaptation curves were obtained from 4 mallard ducks. A curve of best fit was used to compare the mallards' mean adaptation curve to the curve previously reported for the black-bellied tree duck, a crepuscular species. The curves did not differ significantly in either their slopes or base levels (thresholds). The mallards curve had a rod-cone "break" at approximately 25 min. This break is evident in the scotopic curve for pigeons, but is absent from the black-bellied tree ducks' curve. Examination of retinal tissues indicated that the black-bellied tree ducks had significantly more rods and cones, and a larger rod:cone ratio than the mallards. The mallards' scotopic visual threshold is exceeded by the natural illumination present under several nocturnal conditions.     

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.     

Saturation of light mixtures as a function of chromatic and achromatic excitation in the visual system

Summary The saturation of mixtures of white and chromatic lights may be measured by magnitude estimation as a function of the proportion of chromatic light in the mixture. When the intensity of the white light is kept constant, and the intensity of the chromatic light is varied, the psychophysical saturation curves change in a regular way: With higher chromatic intensity, they become less convex, and finally turn concave. Therefore it is possible to measure a whole class of stimulus-response curves representing the relation of chromatic light proportion to saturation. In this paper, a hyperbolic function is developed to describe this class of curves. The function is based upon the assumption that the data-processing system of human color vision evaluates the proportion of chromatic and achromatic excitation to produce subjective saturation. This assumption is in accordance with the known constancy of color perception under natural viewing conditions. The experimental data are approximated just as well, and in some cases better, by the hyperbolic function than by the commonly used power function.     

The effects of illumination level and retinal size on the depth stratification of subjective contour figures

The apparent stratification in depth of subjective contour figures over their backgrounds was investigated as a function of illumination level, figure size, and viewing distance. Magnitude estimation, with a real contour figure serving as the modulus, was used to measure the stratification in depth of a subjective contour figure over its background. Illumination level and retinal size both had significant effects on the depth stratification of the subjective contour figures. The greatest apparent depth differences were obtained for figures of small retinal size under low levels of illumination. These results paralleled previous findings for judgments of subjective contour strength. Consequently, both contour clarity and depth stratification of subjective contour figures are affected in similar ways by illumination level, figure size, and viewing distance. The implications of this response coupling are discussed in terms of current theories of subjective contours.     

Dark adaptation and short-wavelength backgrounds decrease perceived size.

The effects of background luminance, contrast, and background wavelength on the perceived size of small line figures were studied at mesopic levels of light adaptation. Perceived size diminished at low levels of background luminance. The effect disappeared at high levels of luminance. Perceived size of luminous circles increased as a logarithmic function of background luminance when the background intensity did not exceed 25 td(1). The strength of the size effect decreased as a function of circle diameter from 0-125 to 2 deg of visual angle(2). Perceived size of small luminous circles, subtending less than 0-5 deg, also increased as a function of contrast at low values of contrast but at very high values of contrast there was a decrease in perceived size. Background luminance had the same effect on the perceived size of circles as on the perceived size of spatial cycles in gratings. Control experiments led to the conclusion that dark adaptation is the primary source of the size effects. The main evidence for this conclusion was obtained from a demonstration that the same background luminance produced either an increase or a decrease in perceived size, depending on the adaptational state of the eye. It was also found that a shift from cone vision to rod vision contributes to the effects, for a stimulus looked smaller on a short-wavelength background than on a long-wavelength background. The size effects can be predicted from the changes of receptive-field properties of single neurones under corresponding conditions of stimulation, if it is assumed that the perception of size is mediated by size-specific channels formed of single neurones. Stimulation that leads to an activation of small receptive fields appears to indicate to the brain the presence of small retinal images. If small receptive fields are experimentally made responsive to larger retinal images, an underestimation of size results.     

Brightness interactions between rods and cones

Two parafoveal test targets with different spectral compositions were matched in brightness to a fixed-luminance foveal reference target under scotopic adaptation conditions. The idea of the experiment was to find a reference luminance for which one of the matching test targets stimulated only rods while the other stimulated both rods and cones. If brightness was proportional to the linear sum of rod and cone responses, then the luminance of the matching rod+cone target would be predictably closer to rod threshold than would that of the rod target. The results were complicated by evidence that rod responses to the test targets selectively enhanced weak chromatic signals. Nevertheless, it was possible to show that cone activity never reduced the matching luminance as much as predicted by the additivity hypothesis, and sometimes even increased it. These findings suggest that cone activity can suppress brightness signals from rods.     

Double flashes from single pulses of light

Under some conditions, a single pulse of light appears as two. The following parameters of the double-flash phenomenon were studied in two experiments: room illumination, stimulus size, peripheral angle of viewing, latency between the two flashes, and flash wavelength. It was found that the phenomenon only appeared consistently under mesopic levels of white or green illumination and from 13 to 55 deg peripherally. The mean latency between the flashes was estimated at 104 msec. The data are considered to support an explanation in terms of differential latency between the rod and cone systems.     

Hue discrimination in peripheral vision under conditions of dark and light adaptation

Rod interference is a possible factor contributing to the elevation of chromatic threshold in peripheral vision. It was found that light adaptation lowered peripheral chromatic thresholds. This result was interpreted as being due to the lowering of rod sensitivity. It was also found that light in the photochromatic interval appeared blue, indicating that rods may add a blue component to peripheral color vision.     

The influence of depth segmentation on colour constancy

In real scenes, surfaces in different depth planes often differ in the luminance and chromatic content of their illumination. Scene segmentation is therefore an important issue when considering the compensation of illumination changes in our visual perception (lightness and colour constancy). Chromatic adaptation is an important sensory component of colour constancy and has been shown to be linked to the two-dimensional spatial structure of a scene (Werner, 2003 Vision Research 43 1611 - 1623). Here, the question is posed whether this cooperation also extends to the organisation of a scene in depth. The influence of depth on colour constancy was tested by introducing stereo disparity, whereby the test patch and background were perceived in either the same or one of five different depth planes (1.9-57 min of arc). There were no additional cues to depth such as shadows or specular highlights. For consistent illumination changes, colour constancy was reduced when the test patch and background were separated in depth, indicating a reduction of contextual influences. An interaction was found between the influences of stereo depth and spatial frequency on colour constancy. In the case of an inconsistent illumination change, colour constancy was reduced if the test patch and background were in the same depth plane (2-D condition), but not if they were separated in depth (3-D condition). Furthermore, colour constancy was slightly better in the 3-D inconsistent condition than in the 2-D inconsistent condition. It is concluded that depth segmentation supports colour constancy in scenes with inconsistent illumination changes. Processes of depth segmentation are implemented at an early sensory stage of colour constancy, and they define visual regions within which the effects of illuminant changes are discounted for separately. The results support recent models that posit such implementation of scene segmentation in colour constancy.     

Illumination change at a depth edge can reduce lightness constancy

Lightness constancy requires that a surface retain its lightness not only when the illumination is changed but also when the surface is moved from one background to another. Occlusion of one surface by another frequently results in a retinal juxtaposition of patches under different illuminations. At such edges, retinal luminance ratios can be much higher than in scenes with a single illumination. We demonstrate that such retinal adjacencies can produce failures of lightness constancy. We argue that they are responsible for departures from perfect lightness constancy in two prior experiments that examined the effects of depth relations on lightness constancy.     

The influence of chromatic and achromatic variability on chromatic induction and perceived colour

Judgments of the colour of a surface are influenced by the colour of the surrounding. To determine whether only the average colour of the surrounding matters, or also the chromatic variability, judgments in colourful scenes are often compared with ones in which a target is surrounded by a plain background that provides the same average physical illumination of the retina as the colourful scene. The variability sometimes makes a difference (eg Shevell and Wei, 1998 Vision Research 38 1561-1566), and sometimes it does not (eg Brenner and Cornelissen, 1998 Vision Research 38 1789-1793). Is this because of the nonlinearity in cone responses? We designed scenes that stimulated the cones in an equivalent manner, both on average and in terms of variability, and yet differed markedly in chromatic variability. The more colourful surroundings had considerably less influence on subjects' colour judgments. We conclude that early cone-specific regulation of sensitivity cannot be responsible for the change in perceived colour, and deduce that chromatic induction takes place after contrast gain control.     

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.     

颜色知觉恒常理论的回顾

本文对早期颜色恒常理论、系数理论、计算理论和 Octant模型作了简要回顾 ,并结合已有的研究成果进行评述。对影响颜色恒常性机制的主要因素进行了探讨。强调了知觉经验、记忆、认知决策等高级意识活动对颜色恒常知觉的作用 ,并尝试性地提出了描述颜色恒常知觉过程的一般参照框架。     

Perception of depth: Different processing times for simple and relative positional disparity

Summary When judging in stereoscopic vision whether an object is lying in front of or behind the point of momentary fixation, the visual system extracts depth information by using retinal disparity; in this case it computes one angular difference between retinal images (simple positional disparity). But if the task is to discriminate two or more objects in their depth (relative to the point of fixation) and the relative distances between them, two or more such angular differences have to be determined (relative positional disparity). An investigation was carried out to determine whether depth extraction is more complex for relative distances than for object positions and therefore demands a longer processing time. For this purpose stimuli with simple and relative positional disparity were foveally and parafoveally presented (each followed by a masking stimulus). It was shown that the duration threshold for the detection of stimuli with relative disparity was about 2.5 times larger than that for stimuli with simple disparity (Exp. 1). This difference could not be attributed to differences in stimulus configuration between simple and relative disparity (Exp. 2). The results are discussed in terms of a serial, hierarchically structured, disparity processing.     

Stereoacuity for oscillating targets exposed through apertures of various horizontal ex tents

This experiment assesses the separate effects of several interrelated temporal variables on binocular depth discrimination as measured in a two-rod test apparatus. Equidistance settings were obtained from two Ss for a black target oscillating in a frontal plane at each of five velocities, and viewed against a constant illuminated background (1.20 log td) through 29 different horizontal apertures. Combinations of target velocities and aperture sizes were selected to produce a series of eight constant target viewing times (0.15, 0.25, 0.40, 0.50, 0.80, 1.00, 1.50, and 2.00 sec). Both the constant and the variable errors of the equidistance settings were analyzed in terms of the relative deleterious effects produced by increased target velocity and reduced horizontal aperture. The deleterious effects were discussed with respect to the contribution of presumed loss in neural integration for the changing luminous-energy distribution patterns on each retina, energy losses occurring in each pair of stimulated binocular retinal elements along the path of image movement, decreases in target viewing time, and reduction in the number of binocular retinal elements being stimulated.