Glowing greys and surface-white: the photo-geometric factors of luminosity perception

The perception of luminosity is thought to depend upon the intensity of the stimulus: a surface begins to appear self-luminous when it emits or reflects a certain amount of light. This is known as the luminosity threshold. It is a common opinion among vision scientists that such a threshold is correlated to the intensity of a perceptually white surface, in the sense that only an area of the visual field with luminance higher than perceived surface-white will appear luminous. Here we show grey colours that appear luminous in virtue of surrounding luminance ramps. These ramps are intended to mimic halos seen around light sources in natural environments. The results of three experiments indicate that the phenomenon is in direct contradiction to the aforementioned assumptions and suggest the existence of separate perceptual pathways for self-luminosity perception and for surface-colour perception.     

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.     

When figure-ground segmentation modulates brightness: the case of phantom illumination

In the phantom illumination illusion, luminance ramps ranging from black to white induce a brightness enhancement on an otherwise homogeneous dark background. The strength of the illusion was tested with regard to the extension of the brightness inducing perimeter, surrounding the target area by manipulating the number of inducers (exp. 1) and the size of the inducers (exp. 2). Participants' task was to rate the difference in brightness between the target area and the background. Results show that the illusion occurs only when the target area is not completely segregated from the background by luminance ramps; vice versa, when the target area is delimited by a continuous gradient, it appears darker than the background. These findings suggest a major role of figure-ground organization in the appearance of the illusion. This hypothesis was tested in a rating task experiment with three types of target area shapes circumscribed by four types of edges: luminance contours, illusory contours, no contours, and ambiguous contours. Illusory contours, just as luminance contours, hinder the illusion and produce a darkening of the target area. A control experiment measured the brightness of the previous stimuli without luminance ramps: all configurations resulted in a darkening of the target area. Results from all experiments suggest that figure-ground segmentation plays a major role in the determination of both illumination and lightness in stimuli with luminance gradients.     

The phantom illumination illusion

A novel brightness illusion in planar patterns is reported. The illusion occurs, for example, when surfaces with a luminance ramp shaded from black to white are positioned on a black homogeneous background, so that each white end of the surfaces faces a single point of the plane of the pattern. The illusion consists of the enhancement of the brightness of the background in a relatively wide area around the white ends of the surfaces. A parametric study was conducted in which participants were asked to rate the difference in brightness between the parts of the background inside and outside a virtual circle formed by disks with different luminance ramps. The results show that mean ratings of brightness depended on the luminance of the background, the luminance range of ramps, and the kind of ramp. Discussion of these results with reference to other brightness illusions (assimilation, neon color spreading, anomalous surfaces, visual phantoms, grating induction, and the glare effect) shows that t hephantom illumination illusion derives from processes producing the perception of ambient illumination.     

The glare effect and the perception of luminosity

The impression of self-luminosity in the glare effect was studied in two experiments. In experiment 1 the target (CS) was set to the highest luminance of the field and subjects were asked to adjust the luminance ramp of the inducers (R) against five backgrounds (B) to the point where they began to see CS as self-luminous. It was found that there is a linear relationship between background and luminance ramp. Another group of subjects carried out the same task in experiment 2, but this time CS and R were linked together so that CS would always have the same luminance as the highest luminance level of R, as adjustments were performed. It was found that: (i) adjustments were always lower than the highest luminance available; (ii) the linear relationship between background and luminance ramp was confirmed; (iii) observers reported a compelling impression of self-luminous grays. Data are discussed in relation to Bonato and Gilchrist's model for the perception of luminosity. The authors advance the hypothesis that luminance ramps are used at an early stage of encoding for the perception of luminosity.     

Near-field visual acuity of pigeons: effects of head location and stimulus luminance.

Two pigeons were trained to discriminate a grating stimulus from a blank stimulus of equivalent luminance in a three-key chamber. The stimuli and blanks were presented behind a transparent center key. The procedure was a conditional discrimination in which pecks on the left key were reinforced if the blank had been present behind the center key and pecks on the right key were reinforced if the grating had been present behind the center key. The spatial frequency of the stimuli was varied in each session from four to 29.5 lines per millimeter in accordance with a variation of the method of constant stimuli. The number of lines per millimeter that the subjects could discriminate at threshold was determined from psychometric functions. Data were collected at five values of stimulus luminance ranging from--0.07 to 3.29 log cd/m2. The distance from the stimulus to the anterior nodal point of the eye, which was determined from measurements taken from high-speed motion-picture photographs of three additional pigeons and published intraocular measurements, was 62.0 mm. This distance and the grating detection thresholds were used to calculate the visual acuity of the birds at each level of luminance. Acuity improved with increasing luminance to a peak value of 0.52, which corresponds to a visual angle of 1.92 min, at a luminance of 2.33 log cd/m2. Further increase in luminance produced a small decline in acuity.     

Interference in the perceived segregation of equal-luminance element-arrangement texture patterns

Perceived segregation in element-arrangement patterns composed of squares of equal size and luminance, but of two different hues, was investigated in two experiments. Element-arrangement patterns consist of two types of elements, arranged in alternating vertical stripes in the top and bottom regions and in a checkerboard pattern in the center region. Perceived segregation of the striped and checkerboard regions decreased with increasing luminance of the interspaces between the squares, a high-luminance surround, and the increased spacing of the squares. When the luminance of the horizontal interspaces was increased, the decrease in perceived segregation was greater than that when the luminance of the vertical interspaces was increased. Two explanations of the interference of the interspace luminance are discussed. One explanation is in terms of inhibitory interactions among cortical filters tuned to spatial frequency and orientation. A second explanation is in terms of interference with preattentive grouping processes.     

Linking dynamical perceptual decisions at different levels of description in motion pattern formation: psychophysics

The relationship between local-level motion detection and higher level pattern-forming mechanisms was investigated with the motion quartet, a bistable stimulus for which either horizontal or vertical motion patterns are perceived. Local-level perturbations in luminance contrast affected the stability of the perceived patterns and, thereby, the size of the pattern-level hysteresis obtained by gradually changing the motion quartet's aspect ratio. Briefly eliminating luminance contrast (so nonmotion was perceived during the perturbation) eliminated pattern-level hysteresis, and briefly increasing luminance contrast (so motion was perceived during the perturbation) increased pattern-level hysteresis. Partially reducing luminance contrast resulted in bistability during the perturbation; pattern-level hysteresis was maintained when motion was perceived, and eliminated when nonmotion was perceived. The results were attributed to local motion/nonmotion perceptual decisions in area V1 affecting the magnitude of the activation feeding forward to motion detectors in area MT, where the stability of pattern-level perceptual decisions is determined by activation-dependent, future-shaping interactions that inhibit soon-to-be-stimulated detectors responsive to competing motion directions.     

Expectancy and visual-spatial attention: effects on perceptual quality

When we expect important stimuli at a particular spatial location, how does our perceptual sensitivity change over space? Subjects were cued to expect a target stimulus at one location and then required to perform one of the following tasks at that and three other locations: luminance detection, brightness discrimination, orientation discrimination, or form discrimination. The analysis of subjects' performance according to signal detection theory revealed changes in both sensitivity and bias for each of these tasks. Sensitivity was maximally enhanced at the location where a target stimulus was expected and generally decreased with distance from that location. Factors that influenced the gradient of sensitivity were (a) the type of task performed and (b) the spatial distribution of the stimuli. Sensitivity fell off more steeply over distance for orientation and form discrimination than for luminance detection and brightness discrimination. In addition, it fell off more steeply when stimuli were near each other than when they were farther apart.     

Transient covert attention does alter appearance: a reply to Schneider (2006)

We recently demonstrated that transient covert attention increases the apparent contrast of a stimulus (Carrasco, Ling, & Read, 2004). Schneider (2006) proposes that the observed increase in apparent contrast is largely due to sensory interactions occurring between the precue a nd stimulus,rather than to attention. Specifically, hereports that cuing effects only occur at contrasts ne ar detection threshold, and that there a re confounding sensoryinteractions between the cue and stimulus at suprathreshold detection contrasts. Our response is twofold. First, we outline the key methodological differences between our original study and Schneider's that are likely to account for the different results, and explain how we had ruled out the sensory interaction explanation of the cue. Second, we directly test the prediction put forth by Schneider. If the effects were due to sensory interactions, reversing the luminance polarity of the precue in our paradigm should lead to differential cuing effects. We replicate one of the experiments of our original study and add a condition in which the cue luminance is either black or white. Our results replicated our previous findings-they showed an increase in apparent contrast to a high-contrast stimulus when it was precued. Moreover, we found that the black cue and the white cue had the same effect, thus ruling out the alternative explanation proposed by Schneider. Transient attention does alter contrast appearance.     

The attentional dynamics of masked detection

A dichoptic masking procedure was used to test whether the mask-dependent cuing effects found in luminance detection by P. L. Smith (2000a) were due to integration masking or interruption masking. Attentional cuing enhanced detection sensitivity (d') when stimuli were backwardly masked with either dichoptic or monoptic masks, whereas no cuing effect was found with unmasked stimuli, implying the mask dependencies were due to interruption of stimulus processing in visual cortex by the mask. The effect is predicted by a gated diffusion process model in which masks interrupt stimulus processing and attention controls the flow of information to a sequential-sampling decision mechanism. The model correctly predicts different patterns of performance for detection and discrimination and cuing effects in simple reaction time.     

Attention-based texture segregation

Luminance- or color-defined +/- 45 degrees-oriented bars were arranged to yield single-feature or double-conjunction texture pairs. In the former, the global edge between two regions is formed by differences in one attribute (orientation, or color, or luminance). In the color/orientation double-conjunction pair, one region has +45 degrees red and -45 degrees green textels, the other -45 degrees red and +45 degrees green textels (the luminance/orientation double-conjunction pair is similar); such a pair contains a single-feature orientation edge in the subset of red (or green) textels, and a color edge in the subset of +45 degrees (or -45 degrees) textels. We studied whether edge detection improved when observers were instructed to attend to such subsets. Two groups of observers participated: in the test group, the stimulus construction was explained to observers, and they were cued to attend to one subset. The control group ran through the same total number of sessions without explanations/cues. The effect of cuing was week but statistically significant. Feature cuing was more effective for color/orientation than for luminance/orientation conjunctions. Within each stimulus category, performance was nearly the same no matter which subset was attended to. On average, a global performance improvement occurred over time even without cuing, but some observers did not improve with either cuing or practice. We discuss these results in the context of one-versus two-stage segregation theories, as well as by reference to signal enhancement versus noise suppression. We conclude that texture segregation can be improved by attentional strategies aimed to isolate specific stimulus features.     

Color discrimination and luminance

This experiment studied the relation between luminance level and color discrimination at 570 millimicrons. A variety ofstimuli whose luminances varied from .1 to 100 ft-L were viewed against a variety of surrounds. 1t was found that color discrimination ability was a joint function of the luminance level of the stimulus and the ratio of the luminance of the stimulus to that of the surround.     

Visible persistence following a brief increment in stimulus luminance

In previous studies, it has been demonstrated that visible persistence--the period for which the perceived duration of a stimulus exceeds its physical duration--can be extended by briefly incrementing the luminance of the stimulus immediately prior to offset. Using a two-component pattern integration task, we show that this effect is not an artifact of change in the total luminous flux within the stimulus. Visible persistence was unaffected by overall luminance of the stimulus. It was also time-locked to the luminance increment. Visible persistence is seen to result from a process that is initiated by stimulus onset and that can be either wholly or partially reinitiated by the onset of the luminance increment. The duration of this process (which determines the duration of stimulus visibility) can be modified in a graded fashion by stimulus events that occur after its initiation. We outline a single-process inhibitory feedback model of the persistence mechanism that accounts for the present findings.     

The effects of stimulus numerosity,retinal location,and rod contrast on perceived duration of brief visual stimuli

The effects of manipulating three stimulus parameters were determined on a standard perceived duration task using 40- and 70-msec visual stimuli. In Experiment 1, it was found that perceived duration increased with increasing number of target dots but decreased as the area that contained the dots also increased. Experiment 2 examined the effect of varying the retinal location (0, 2, or 4 deg from fovea) of the target dot and found perceived target duration to increase with increasing eccentricity. In Experiment 3, the background luminance for a constant red target was varied so as to alter the scotopic contrast of the target. Perceived duration was minimal for the scotopically matched target and background conditions. The results of all three experiments were discussed in terms of important retinal—and even rod—contributions to tasks of perceived duration.     

The role of transparency in perceptual grouping and pattern recognition.

The shortest stimulus exposure time for which transparency can be seen was examined. In the first experiment, overlapping digits were presented for 120 ms and the luminance in the overlapping regions was varied. Subjects reported, in separate blocks of trials, either the apparent transparency of the digits or the identity of the digits. When the luminance was set so that one set of digits appeared to be seen through the other, recognition of the digits was high. When the luminance in the overlapping regions did not produce impressions of transparency, digit recognition was low. In the second experiment, digit identification at several stimulus durations was compared between stimuli that had luminance that was valid for transparency and stimuli that had invalid luminance. Performance was found to be higher in the valid luminance condition than in the invalid condition after as little as 60 ms exposure duration. This result suggests that the impression of transparency requires only relatively short exposure durations.     

Anatomy of a flash. 2. The 'width' of a temporal edge.

In a previous study it has been found by using the Crawford masking paradigm with spatially coextensive stimuli that the end points of even a weak flash have a strong masking effect on the probe pulse, but no threshold elevation was observed when the probe was 100 ms or longer from flash onset and offset. The relationship between the strength of a temporal edge (eg the amplitude of a sudden increase in field luminance) and the duration of masking has not been systematically investigated. In the present experiments the duration of masking produced by a step of luminance as a function of step size was measured. With steps whose amplitude was between ten and five hundred times detection threshold, the duration of masking was about constant, ie 70 and 50 ms for on-responses and off-responses, respectively. This refractory period defined the 'width' of a temporal edge. Unless two suprathreshold unidirectional luminance changes are separated by an interval exceeding the width of a temporal edge, they are perceived as a single change in brightness. A linear systems analysis led to predictions for ramp stimuli that were confirmed by experiment.     

Does segregation by colour/luminance facilitate the detection of structure-from-motion in noise?

The aim in the experiments was to examine whether the detection of structure-from-motion (SFM) in noise was facilitated when target and noise were segregated by colour and/or luminance polarity. The SFM target was a rotating 'V-shape' structure simulated with limited-lifetime Gaussian micropatterns and embedded in random-motion noise. Threshold levels of V-shape slant were measured for stimuli in which target and noise were segregated or unsegregated by colour/luminance, and under two conditions, with and without static form cues to the SFM target. The presence or absence of static form cues to the SFM target was manipulated by varying the relative numbers of micropatterns in target and noise. In the absence of static form cues, segregation of target and noise by colour and/or luminance polarity did not facilitate target detection, even when subjects knew which micropatterns belonged to the target. On the other hand, when static form cues were present, segregation improved performance. These results imply that SFM processing is 'form-cue invariant' except when the target form is immediately identifiable in the static view of the stimulus. The significance of the results for understanding the role of colour vision in breaking camouflage and in 'grouping' is discussed.     

Processing time of contour integration: the role of colour, contrast, and curvature

We investigated the temporal properties of the red - green, blue-yellow, and luminance mechanisms in a contour-integration task which required the linking of orientation across space to detect a 'path'. Reaction times were obtained for simple detection of the stimulus regardless of the presence of a path, and for path detection measured by a yes/no procedure with path and no-path stimuli randomly presented. Additional processing times for contour integration were calculated as the difference between reaction times for simple stimulus detection and path detection, and were measured as a function of stimulus contrast for straight and curved paths. We found that processing time shows effects not apparent in choice reaction-time measurements. (i) Processing time for curved paths is longer than for straight paths. (ii) For straight paths, the achromatic mechanism is faster than the two chromatic ones, with no difference between the red-green and blue-yellow mechanisms. For curved paths there is no difference in processing time between mechanisms. (iii) The extra processing time required to detect curved compared to straight paths is longest for the achromatic mechanism, and similar for the red - green and blue-yellow mechanisms. (iv) Detection of the absence of a path requires at least 50 ms of additional time independently of chromaticity, contrast, and path curvature. The significance of these differences and similarities between postreceptoral mechanisms is discussed.     

Effects of similarity on apparent motion and perceptual grouping

Effects of similarity in colour, luminance, size, and shape on apparent motion and perceptual grouping were examined in part 1 in two parallel experiments on the same seven subjects. In both experiments, the effect of similarity was compared with that of proximity in competitive, bistable stimulus situations. A combination of a larger horizontal separation between the homogeneous stimulus elements and a smaller constant vertical separation between heterogeneous stimulus elements produced two kinds of apparent motion (or perceptual grouping) with equal probabilities. Such matched separations between homogeneous stimulus elements were obtained by the double staircase method in various stimulus conditions. In both experiments on apparent motion and perceptual grouping matched separation was found to increase as the difference between the heterogeneous stimulus elements increased. High correlations (0.71 to 0.94) of matched separations were found between apparent motion and perceptual grouping in four stimulus series: colour, luminance, size, and shape. Six of the seven subjects were also tested in part 2. Here, the effects of differences were found to work additively across different perceptual attributes in both phenomena, when multiple differences were combined in heterogeneous elements. The experimental results are discussed from the point of view that apparent motion is an example of perceptual constancy.