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.     

Light and dark adaptation of visually perceived eye level controlled by visual pitch

The pitch of a visual field systematically influences the elevation at which a monocularly viewing subject sets a target so as to appear at visually perceived eye level (VPEL). The deviation of the setting from true eye level averages approximately 0.6 times the angle of pitch while viewing a fully illuminated complexly structured visual field and is only slightly less with one or two pitched-from-vertical lines in a dark field (Matin & Li, 1994a). The deviation of VPEL from baseline following 20 min of dark adaptation reaches its full value less than 1 min after the onset of illumination of the pitched visual field and decays exponentially in darkness following 5 min of exposure to visual pitch, either 30° topbackward or 20° topforward. The magnitude of the VPEL deviation measured with the dark-adapted right eye following left-eye exposure to pitch was 85% of the deviation that followed pitch exposure of the right eye itself. Time constants for VPEL decay to the dark baseline were the same for same-eye and cross-adaptation conditions and averaged about 4 min. The time constants for decay during dark adaptation were somewhat smaller, and the change during dark adaptation extended over a 16% smaller range following the viewing of the dim two-line pitched-from-vertical stimulus than following the viewing of the complex field. The temporal course of light and dark adaptation of VPEL is virtually identical to the course of light and dark adaptation of the scotopic luminance threshold following exposure to the same luminance. We suggest that, following rod stimulation along particular retinal orientations by portions of the pitched visual field, the storage of the adaptation process resides in the retinogeniculate system and is manifested in the focal system as a change in luminance threshold and in the ambient system as a change in VPEL. The linear model previously developed to account for VPEL, which was based on the interaction of influences from the pitched visual field and extraretinal influences from the body-referenced mechanism, was employed to incorporate the effects of adaptation. Connections between VPEL adaptation and other cases of perceptual adaptation of visual direction are described.     

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.     

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.     

Brightness exponent as a function of retinal eccentricity in the peripheral visual field: Effects of dark and light adaptation

Using a method of direct magnitude estimation, the exponent of the brightness power function was determined under dark and light adaptation at luminance levels well above threshold. The exponent was estimated for functions describing the brightness of stimuli presented at the fovea and the following peripheral retinal loci: 10, 20, 30, 40, and 50 deg nasally eccentric to the fovea along the horizontal meridian of the right eye. The exponent for a 1-sec flash was found to be approximately .33 at the fovea and increased slightly with increasing retinal eccentricity.The effect of adaptation on the brightness exponent was not so large when the target luminance was set well above threshold.     

卡车驾驶员的夜间视力研究

运用ＹＪＳ—ＩＩ型夜间视觉检查仪对２３８名男性卡车驾驶员的暗适应时间和夜间视力进行了测试。结果表明：卡车驾驶员暗适应时间的９５％上限值为５９．６７秒;卡车驾驶员暗适应时间和夜间视力的年龄阈值为４０岁;事故组与安全组卡车驾驶员暗适应时间存在显著差异（Ｐ＜０．０５）,事故组卡车驾驶员的暗适应时间较长,表明卡车驾驶员的暗适应能力差是引起夜间交通事故的重要因素。研究结果为驾驶员的选拔,安全教育以及制订预防夜间交通事放对策提供一定的理论依据。     

COLOR THRESHOLD MEASUREMENTS IN SCOTOPIC VISION

The absolute and the color threshold in scotopic vision generally coincide during dark adaptation, indicating that color-threshold intensity is a measure of the concentration of rhodopsin, and that different modes of rhodopsin regeneration are reflected in the measurements of the color threshold.     

Dark adaptation and the Hermann grid illusion

The latency of the perception of the dark spot at the intersection of a Hermann grid was measured before and after dark adaptation. It was found that dark adaptation significantly increased the latency of perception of the spot while light adaptation had no effect. This finding was predicted from the Jung and Spillman account of the Hermann grid illusion and from the Kuffler et al. finding that inhibitory receptive fields of the cat’s retinal ganglion ceils are reduced in size and responsiveness after dark adaptation. The significance of this finding in relation to other simultaneous contrast phenomena is discussed.     

Visual influence on taste sensitivity

A claimed dependence of taste sensitivity on body state, accepted for 40 years, is investigated in two experiments. Neither the growth of sensation above threshold, as measured in a magnitude estimation experiment, nor taste sensitivity near threshold, as measured by a signal detection analysis, show the claimed increment when individuals are dark-adapted. On the contrary, in both cases, performance is superior in the light, when subjects taste with their eyes open, possibly due to an arousing effect of concurrent visual stimulation.     

Reexamination of spectral mechanisms in the rat (Rattus norvegicus)

The spectral mechanisms of the rat were studied in electrophysiological and behavioral experiments. The photopic electroretinogram (ERG) was recorded (a) to rapidly flickering lights, (b) during the cone phase of dark adaptation, and (c) with a flicker photometric procedure. Each procedure indicated the presence of a single cone mechanism having a lambda max of about 510 nm. Increment-threshold spectral sensitivity functions measured in a behavioral test situation yielded the same conclusion. A behavioral experiment failed to produce any evidence for the presence of color vision in this rodent. The consistent conclusion from both behavioral and electrophysiological experiments is that the rat retina contains only a single photopic spectral mechanism.     

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.     

Long-term rod dark adaptation in man. Threshold measurements, rhodopsin regeneration and allosteric sensitivity regulation. An evaluation

Recent evidence strongly suggests that the relationship between threshold elevation ( T ) and fraction of bleached rhodopsin ( B ), obtained during a major, middle period of long-term rod dark adaptation in man, is well described by a power function, i. e., T = k · Bⁿ , where k is a multiplicative constant and n is the exponent. Due primarily to the low reliability of measurements of rhodopsin regeneration, however, the exponent n of the power function cannot, at present, be given an exact value. Available information indicates that the value of the exponent ranges between 2.4 and 4. Implications of this uncertainty are discussed within the framework of the allosteric, tetrameric model of rod dark adaptation. It is concluded that this model in its simplest form may only offer a first approximation of the real system implicated in the process.     

Olfactory adaptation and recovery in old age

Four experiments are reported in which it is shown that elderly adults are more prone than young adults to olfactory adaptation and are slower to recover threshold sensitivity. The first three experiments differed in detail, but had in common an initial threshold determination for 1-butanol, a 30 s exposure to a concentration twenty-seven times threshold, followed by repeated presentation of the initial threshold level at various intervals after adaptation. In three experiments accuracy of forced-choice discrimination was poor immediately after adaptation but tended to improve with time, and considerably faster in the young than in the elderly. In the fourth experiment, groups of twenty-three elderly and twenty-five young subjects threshold-matched for pyridine were compared. The subjects participated in three sessions in which pyridine was infused into a test chamber at either 2.5, 1.25, or 0 L min-1 (sham session). At 2.5 L min-1 both groups were able to track the buildup of odor intensity during infusion and its decline after infusion. In contrast, at 1.25 L min-1 only the young were able to track odor intensity, even though the concentration rose above initial threshold levels.     

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.     

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.     

Dark-adaptation mechanisms of the long-wave foveal cones

The ordinary long-term rod and cone dark-adaptation curves have generally been assumed to follow a single exponential rate of recovery. However, in two previous papers on rod dark-adaptation (Stabell et al., 1986a, b), the recovery curve was found to consist of three different sections. The results of the present paper show the same type of recovery function with three different sections for the long-term dark-adaptation curve of the long-wave cone system. During the major, middle section log cone threshold, like log rod threshold, is linearly related to the logarithm of the concentration of bleached photopigment. Presupposing that the bleached cone photopigment acts as a ligand, the change in threshold level obtained during the middle section of the dark-adaptation curve is well described by the change in activity rate of an allosteric, postively cooperative enzyme built as a dimer.     

The apparent length of rotating arcs under conditions of dark adaptation

The apparent contraction of a rotating light arc occurred during the first 20 rain, but not after 25 min, of dark adaptation. Estimates of length obtained after 25 min were affected by the level of luminance of the arc but not by its speed of rotation, by dark gaps in the arc, or by instructions to estimate its length in terms of a brighter region. There was no tendency for a rotating dark arc to appear shorter at any stage of 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.     

The perceptual onset of musical tones

The perceptual onset of a musical tone can be defined as the moment in time at which the stimulus is first perceived. In the present experiments, a simple threshold model for the perceptual onset was applied. A paradigm was used in which a sequence of tones had to be adjusted in such a way that the onsets were perceived at equally spaced moments in time. In Experiment 1, the threshold model was applied in a design in which the rise times of the tones were varied. We concluded that the perceptual onsets of the tones can, indeed, be defined as the times at which the envelopes pass a relative threshold of 15 dB below the maximum level of the tones (82 dB). In Experiment 2, the maximum levels of the tones were varied from 37 to 77 dB. The results show that there is a shift in the relative threshold, but that this shift is small relative to the shift in the stimulus level. In Experiment 3, the effect of level above masked threshold on the perceptual onset was investigated in more detail by varying the level of a background noise. The results show that the relative threshold decreases with increasing level above masked threshold. The results from our experiments strongly suggest that the relative threshold is linearly dependent on the level above masked or absolute threshold and that a 7-dB increment of this level results in a 1-dB relative threshold decrement. The threshold model is compared with a current temporal integration model for the perceptual onset of tones. It is shown that our data cannot be adequately explained by temporal integration. Our experimental results suggest that adaptation of the hearing mechanism to a certain relative stimulus level is responsible for perceptual onset. The applicability of our threshold model in various realistic musical situations is discussed.     

Color—luminance relationships and the McCollough effect

The McCollough effect is an orientation-specific color aftereffect induced by adapting to colored gratings. We examined how the McCollough effect depends on the relationships between color and luminance within the inducing and test gratings and compared the aftereffects to the color changes predicted from selective adaptation to different color—luminance combinations. Our results suggest that the important contingency underlying the McCollough effect is between orientation and color—luminance direction and are consistent with sensitivity changes within mechanisms tuned to specific color—luminance directions. Aftereffects are similar in magnitude for adapting color pairs that differ only in S cone excitation or L and M cone excitation, and they have a similar dependence on spatial frequency. In particular, orientation-specific aftereffects are induced for S cone colors even when the grating frequencies are above the S cone resolution limit. Thus, the McCollough effect persists even when different cone classes encode the orientation and color of the gratings.