Achromatic Luminance Research Articles

Lightness Compression and Hue Changes

Two experiments were performed to relate the Bezold-Brücke (B-B) and lightness compression effects. The first used a calibrated screen to present an achromatic luminance staircase. In addition, it reproduced, the methodology and the essential aspects the lightness compression effect discovered by Cataliotti and Gilchrist (1995). That is, observers perceived a truncated grey scale (from white to medium grey) when the staircase was the only stimulation in the near background (Gelb condition), but not when presented on a Mondrian background, because of the high articulation level provided by this background. Experiment 1 design also included two other backgrounds that produced a partial compression effect. In Experiment 2, two chromatic staircases were used. Employing a naming task, changes in hue perception were only observed for the susceptible staircase. The observed changes were of two types. First, for the full staircase presentations, a Gelb background produced maximum lightness compression (more similarity in the lightness of the staircase stimuli) and, also, a minimum B-B effect (fewer differences in hue). Second, only for the Gelb condition, there were changes in the hue of the lowest luminance staircase stimuli depending on the staircase extension. Results are discussed in the framework of the anchoring theory of lightness perception.

V2 Thin Stripes Contain Spatially Organized Representations of Achromatic Luminance Change

A considerable amount of research over the last decades has focused on the apparent specialization of V2 thin stripes for the processing of color in diurnal primates. However, because V2 thin stripes are functionally heterogeneous in that they consist of largely separate color- and luminance-preferring domains and because the color-preferring domains contain a systematic representation of hue, we hypothesized that they contained functional maps that subserve luminance processing. Here we show, using optical imaging of intrinsic cortical signals and microelectrode recording, that the V2 thin stripe luminance-preferring domains contain spatially segregated modules that encode the direction of relative luminance change. Quantitative analysis of the cortical responses to luminance increments or decrements indicates that these luminance-sensitive modules also encode the magnitude of the luminance change by the magnitude of the evoked cortical response. These results demonstrate an important role of V2 thin stripes in the processing of luminance and thus suggest that thin stripes are involved in the overall processing of the surface properties of objects rather than simply the processing of color.

Spectrally opponent inputs to the human luminance pathway: slow +M and −L cone inputs revealed by intense long‐wavelength adaptation

The nature of the inputs to achromatic luminance flicker perception was explored psychophysically by measuring middle- (M-) and long-wavelength-sensitive (L-) cone modulation sensitivities, M- and L-cone phase delays, and spectral sensitivities as a function of temporal frequency. Under intense long-wavelength adaptation, the existence of multiple luminance inputs was revealed by substantial frequency-dependent changes in all three types of measure. Fast (f) and slow (s) M-cone input signals of the same polarity (+sM and +fM) sum at low frequencies, but then destructively interfere near 16 Hz because of the delay between them. In contrast, fast and slow L-cone input signals of opposite polarity (-sL and +fL) cancel at low frequencies, but then constructively interfere near 16 Hz. Although these slow, spectrally opponent luminance inputs (+sM and -sL) would usually be characterized as chromatic, and the fast, non-opponent inputs (+fM and +fL) as achromatic, both contribute to flicker photometric nulls without producing visible colour variation. Although its output produces an achromatic percept, the luminance channel has slow, spectrally opponent inputs in addition to the expected non-opponent ones. Consequently, it is not possible in general to silence this channel with pairs of 'equiluminant' alternating stimuli, since stimuli equated for the non-opponent luminance mechanism (+fM and +fL) may still generate spectrally opponent signals (+sM and +sL).

ビデオ信号（ＥＲ，ＥＧ，ＥＢ）特性を考慮した広範囲輝度分布計測

For the color design of outdoor industrial products, such as cars, models rendered by computer must harmonize with background photographs of each frame of the video sequence in color and shape. This is possible only using high dynamic range luminance corresponding to not only the achromatic luminance signal but also individual video signals (ER, EG, EB). Portability and simplicity are also desired to obtain the data for the luminance distribution corresponding to weather changes. We developed a method for taking digital photos with a fish-eye lens and an ND filters that acquires a complete skylight luminance distribution based on a video signal (ER, EG, EB).

Effective contrast of colored stimuli in the mesopic range: a metric for perceived contrast based on achromatic luminance contrast

Little is known about how color signals and cone- and rod-based luminance signals contribute to perceived contrast in the mesopic range. In this study the perceived contrast of colored, mesopic stimuli was matched with that of spatially equivalent achromatic stimuli. The objective was to develop a metric for perceived contrast in the mesopic range in terms of an equivalent achromatic luminance contrast, referred to here as effective contrast. Stimulus photopic luminance contrast, scotopic luminance contrast, and chromatic difference from the background all contributed to effective contrast over the mid-mesopic range, but their contributions were not independent and varied markedly with background luminance. Surprisingly, color made a significant contribution to effective contrast from 10 to approximately 0.003 cd m(-2). A model describing this relationship is introduced (R2 = 0.89) and compared with predictions of mesopic luminance contrast obtained from a number of models proposed as systems of mesopic photometry.

Interaction of color and geometric cues in depth perception: when does "red" mean "near"?

Luminance and color are strong and self-sufficient cues to pictorial depth in visual scenes and images. The present study investigates the conditions under which luminance or color either strengthens or overrides geometric depth cues. We investigated how luminance contrast associated with the color red and color contrast interact with relative height in the visual field, partial occlusion, and interposition to determine the probability that a given figure presented in a pair is perceived as "nearer" than the other. Latencies of "near" responses were analyzed to test for effects of attentional selection. Figures in a pair were supported by luminance contrast (Experiment 1) or isoluminant color contrast (Experiment 2) and combined with one of the three geometric cues. The results of Experiment 1 show that the luminance contrast of a color (here red), when it does not interact with other colors, produces the same effects as achromatic luminance contrasts. The probability of "near" increases with the luminance contrast of the color stimulus, the latencies for "near" responses decrease with increasing luminance contrast. Partial occlusion is found to be a strong enough pictorial cue to support a weaker red luminance contrast. Interposition cues lose out against cues of spatial position and partial occlusion. The results of Experiment 2, with isoluminant displays of varying color contrast, reveal that red color contrast on a light background supported by any of the three geometric cues wins over green or white supported by any of the three geometric cues. On a dark background, red color contrast supported by the interposition cue loses out against green or white color contrast supported by partial occlusion. These findings reveal that color is not an independent depth cue, but is strongly influenced by luminance contrast and stimulus geometry. Systematically shorter response latencies for stronger "near" percepts demonstrate that selective visual attention reliably detects the most likely depth cue combination in a given configuration.

Long-term maturation of visual pathways.

Previous research in adults has demonstrated the utility of the visual evoked potential (VEP) to measure the integrity of the chromatic and achromatic visual pathways. The VEP has also been shown to be a valuable indicator of maturation of these pathways in infants up to 1 year of age. The present manuscript reports changes in the visual pathways from 2 years to adulthood as measured by the spatio-chromatic VEP. The responses to achromatic reversal stimuli designed to preferentially activate the low spatial-frequency achromatic (luminance) pathways appear adult-like by 1 year of age. The responses to low spatial-frequency isoluminant onset stimuli designed to preferentially activate the chromatic pathway do not appear as they do in the adult until after 12-13 years of age. The shapes of the chromatic VEP waveforms shift from a positive-negative complex to a negative-positive complex. These changes can be modeled by a decrease in the latency of a large negative component between the ages of 1 year and adulthood. The results suggest that for low spatial-frequency stimuli, there are long-term changes in the development of the chromatic pathways that are not observed in the low spatial-frequency achromatic pathways. The changes in the chromatic VEP waveforms with age may be a physiological correlate of reported behavioral changes.

Linear coupling between cerebral blood flow and oxygen consumption in activated human cortex.

The aim of this study was to test the hypothesis that, within a specific cortical unit, fractional changes in cerebral blood flow (CBF) and cerebral metabolic rate of oxygen consumption (CMR(O(2))) are coupled through an invariant relationship during physiological stimulation. This aim was achieved by simultaneously measuring relative changes in these quantities in human primary visual cortex (V1) during graded stimulation with patterns designed to selectively activate different populations of V1 neurons. Primary visual cortex was delineated individually in each subject by using phase-encoded retinotopic mapping. Flow-sensitive alternating inversion recovery MRI, in conjunction with blood oxygenation-sensitive MRI and hypercapnic calibration, was used to monitor CBF and CMR(O(2)). The stimuli used included (i) diffuse isoluminant chromatic displays; (ii) high spatial-frequency achromatic luminance gratings; and (iii) radial checkerboard patterns containing both color and luminance contrast modulated at different temporal rates. Perfusion responses to each pattern were graded by varying luminance and/or color modulation amplitudes. For all stimulus types, fractional changes in blood flow and oxygen uptake were found to be linearly coupled in a consistent ratio of approximately 2:1. The most potent stimulus produced CBF and CMR(O(2)) increases of 48 +/- 5% and 25 +/- 4%, respectively, with no evidence of a plateau for oxygen consumption. Estimation of aerobic ATP yields from the observed CMR(O(2)) increases and comparison with the maximum possible anaerobic ATP contribution indicate that elevated energy demands during brain activation are met largely through oxidative metabolism.

Comparison of color and luminance contrast: apples versus oranges?

Using a spatial, forced-choice, matching protocol, we have measured observers' ability to equate the contrasts of sinusoidal gratings which vary along differing directions in a 3-dimensional color space. In a given experiment, the observer obtained a perceptual match between the contrasts of two gratings whose chromaticities or luminances varied along differing chromatic directions which were selected from among five axes: an achromatic luminance axis (lum), an isoluminant axis where only S-cone activation varied (S-axis), an isoluminant axis where L- and M-cone activation varied in a complementary manner (LM-axis), an axis where only L-cone activation varied (L-axis), and an axis where only M-cone activation varied (M-axis). Even though these chromatic axes were chosen to activate independent mechanisms involved in the early stages of spatiochromatic visual processing, and despite the distinctly differing appearance of patterns from variations along differing directions, we find that observers can reliably make such pairwise contrast matches. Furthermore there is reasonable consistency of matching contrasts among observers and the pairwise contrast matches exhibit the properties of homogeneity and transitivity. This observed homogeneity and transitivity allows, for each color direction, the specification of a single scaling factor which relates perceptual contrast to physical contrast.

Effects of peripheral flicker masking on M- and P-pathway response.

The effects of metahue and metacontrast masking on the responses of the M- and P-pathways of the human visual system were investigated using temporal analysis of the multifocal flash visually evoked potential (VEP) (VERIS system). The experiments were carried out at three achromatic luminance contrasts, 24, 70 and 96%, with three peripheral masks: a steady 65% grey mask, a grey flicker mask and an isoluminant red/green flicker mask. The stimuli were viewed monocularly and the mask and VERIS stimuli superposed with a mirror-aperture system. The masks had no significant effect on the behaviour of the M-pathway as stimulus contrast increased. The amplitude of the P-pathway was found to be approximately level at all contrasts of the stimulus and with all three masks rather than showing the expected steady increase in activity with increasing stimulus contrast.

The separation of parallel visual systems by disease processes.

to investigate psychophysics and electrophysiology in disease states with altered retinal function. determination of colour and luminance contrast sensitivity functions using computer controlled VDUs: recording of flash and pattern ERGs to short and long flashes of coloured lights under differing conditions of light adaptation: recording of pattern ERG. In melanoma-associated retinopathy (MAR) low spatial frequency temporal flicker loss occurs for achromatic Gaussians, but colour Gaussians are seen normally. Low spatial frequency luminance contrast sensitivity and motion losses are severe while red-green gratings are seen normally. In Cuban Tropical Amblyopia, achromatic luminance contrast sensitivity may be normal, in the presence of considerable losses of colour vision, to spatial frequencies as high as 32 c/degree. There are supernormal cone ERGs. these 2 conditions represent highly selective loss of 'M' and 'P' pathways respectively. Almost the entire 'bell shaped curve' normally represents M activity. In CTA, there may be a selective loss of the receptive field surrounds of P ganglion cells.

The Craik-O'Brien-Cornsweet illusion in colour: quantitative characterisation and comparison with luminance.

The strength of the Craik-O'Brien-Cornsweet illusion was measured for different values of spatial and temporal stimulus parameters, in the traditional achromatic version, and in an isoluminant colour version. It was found that the illusion is much weaker with isoluminant colour stimuli than with achromatic luminance stimuli. The illusion depends on the spatial parameters of the stimulus in a way that yields an approximate scale invariance: The strength of the illusion is similar for different stimulus sizes, as long as the ratio of the width of the transition region around the edge, where luminance or colour change, to the total stimulus width is preserved. In both the achromatic and the chromatic case, the strength of the illusion decreases with increasing presentation time. The similarity of the differences between brightness and colour effects on one hand and the differences in sensitivity for colour and luminance changes in humans on the other suggests that a lack of gradient detection underlies the Craik-O'Brien-Cornsweet illusion.

Chromatic and luminance systems deficits in glaucoma

The purpose of this study was to compare the effects of glaucoma, at different stages of the disease process, on the two color-opponent systems and on the luminance system. Discrimination thresholds were measured along the two equiluminant cardinal color axes (RG and YV) and along an achromatic luminance axis (LD) in 27 patients with open-angle glaucoma (OAG) and in 13 glaucoma suspects. Patients with OAG showed increased thresholds along all three axes. The threshold increases correlated significantly with the level of visual field loss. For glaucoma suspects, thresholds were also increased along all three axes. A subgroup of patients with OAG, those with pigmentary glaucoma, showed minimal increases in threshold along the RG axis. To further investigate this finding an additional 15 patients, seven with primary OAG and eight with pigmentary glaucoma were run in a two-alternative forced-choice experiment. For patients with pigmentary glaucoma, thresholds were increased less along the RG axis. The results of the study for OAG patients and glaucoma suspects are consistent with deficits in the two color-opponent systems, and in the luminance system.

Visual evoked potentials in three-dimensional color space: Correlates of spatio-chromatic processing

Visual evoked potentials (VEPs) were measured for sinusoidal gratings with spatio-chromatic modulation defined in a three-dimensional color space. The spatio-chromatic modulation of the gratings can be decomposed into contributions from an achromatic luminance varying component, an isoluminant component which modulates only the activities of L cones and M cones, and an isoluminant component corresponding to modulation of only S-cone activity. The emphasis of this report is the nature of VEPs resulting from isoluminant spatio-chromatic modulation. The VEP response was characterized along a number of spatial, temporal, and chromatic stimulus dimensions: contrast, spatial frequency, chromaticity in the isoluminant plane, chrominance/luminance ratio, orientation, and temporal frequency. Isoluminant VEPs resulting from stimuli modulating L and M cones are compared with those from S-cone modulation. When appropriate spatiotemporal conditions are employed, both types produce robust VEPs; however, the S-pathway VEPs show considerably longer latencies than do those from LM-pathway activation. The VEP results are compared to psychophysical and single unit electrophysiological observations. VEP latencies exhibit the lowpass character of psychophysical chromatic contrast sensitivity functions but VEP amplitudes show bandpass tuning along both the S and LM axes. An oblique effect, i.e. shorter latencies for horizontal and vertical gratings than for diagonal, is observed in the isoluminant VEP. S-pathway VEPs are used to demonstrate an electophysiological correlate of transient tritanopia. Normative amplitude and latency data for VEPs from selectivity stimulated chromatic mechanisms provide a baseline for clinical electrodiagnostic applications.

Transient and sustained components of the pupillary responses evoked by luminance and color

That the pupil reacts to changes in luminance and color, as well as to spatial features in the retinal image raises questions about whether phasic and tonic and/or color and luminance visual pathways project to the pretectal pupillomotor neurons. The present study compares pupillary responses evoked by heterochromatic and achromatic luminance increments to investigate whether the pupillary responses evoked by color and by luminance are independent of one another. Principal component analysis is used to examine the constituents of the pupil responses. The results support the belief that the visual input to the pupillomotor system is organized into phasic and tonic (but not necessarily independent color and luminance) pathways.

Rod-cone dependence of saccadic eye-movement latency in a foveating task

This study examines the relations between some well known oculomotor functions (saccades) and well known retinal physiology (dark adaptation): it deals with the overall latency versus target luminance functions, with the underlying rod and cone latency-luminance functions, and with the synergistic interaction between these latency functions for mesopic targets. Saccadic latency was measured to small lit targets presented at 10 deg retinal eccentricity in complete darkness. Target luminance and wavelength were varied. Additional measurements were made during dark adaptation or on backgrounds, or at different retinal eccentricities. Luminance matched stimuli and Palmer's (1968) equivalent luminance transformation were also used. Latency is determined by an achromatic luminance mechanism that receives substantial rod inputs above the cone threshold. Latencies for pure rod or pure cone inputs increase rapidly as target luminance decreases. For the rods this latency increase appears to represent the waiting time for the 140 or so photons ( λ = 507 nm) that are required for a saccade. Errors in direction occur at scotopic luminances, or at low photopic luminances when only cones are functioning.

Increment thresholds across minimally distinct borders.

The border contour remaining when juxtaposed, heterochromatic fields were equated in luminance by the minimally distinct border (MDB) method was assessed by an increment-threshold technique. In general, the results showed that increment-threshold sensitivity, using a white test probe, did not vary across the chromatic border. A second control experiment, in which the MDB was deliberately offset, demonstrated that increment thresholds reflect achromatic luminance imbalances introduced between heterochromatic fields. This second experiment showed an increase of threshold at the border similar to the Mach-band-like elevations commonly found for fields of dissimilar homochromatic luminance. Both experiments yield results that are consistent with current theory. That is, equating heterochromatic luminance by the MDB technique balances achromatic channels somewhere in the visual system. The chromatic channels, on the other hand, remain imbalanced making the more-saturated field appear brighter. The present work suggests that the increment-threshold method is sensitive only to differences between achromatic channels, not to relative brightness differences due to chromatic-channel imbalance.