Effects of temporal integration on the shape of visual backward masking functions

Many studies of cognition and perception use a visual mask to explore the dynamics of information processing of a target. Especially important in these applications is the time between the target and mask stimuli. A plot of some measure of target visibility against stimulus onset asynchrony is called a masking function, which can sometimes be monotonic increasing but other times is U-shaped. Theories of backward masking have long hypothesized that temporal integration of the target and mask influences properties of masking but have not connected the influence of integration with the shape of the masking function. With two experiments that vary the spatial properties of the target and mask, the authors provide evidence that temporal integration of the stimuli plays a critical role in determining the shape of the masking function. The resulting data both challenge current theories of backward masking and indicate what changes to the theories are needed to account for the new data. The authors further discuss the implication of the findings for uses of backward masking to explore other aspects of cognition.     

Backward masking by pattern stimulus offset

The backward masking effects of the offset of a pattern stimulus on the apparent contrast of a target stimulus were determined to be a function of target onset-mask offset asynchrony. With spatially overlapping stimuli and binocular viewing, a monotonic function similar to that characterizing early dark adaptation was obtained; with a dichoptically presented disk onset as target and a surrounding ring offset as mask, a typical U-shaped metacontrast effect as a function of target onset-mask offset asynchrony was obtained. These mask-offset effects are related to the possible roles of (a) peripheral "off" mechanisms and (b) central metacontrast mechanisms in terminating visual response persistence in sustained channels.     

Spatial extent and figural factors in backward masking

Spatial and figural characteristics of backward masking were studied, with two collinear arcs presented end-to-end and serving as target and mask, respectively. Stimulus onset asynchrony was 50 ms while interstimulus interval was 0 ms. Mask exposure duration required for masking was determined as a function of target length with mask length as a parameter. The exposure duration of the mask required for complete masking varied directly with target length, but inversely with mask length. The fact that masking strength increased with mask duration while all other parameters were kept constant suggests that masking depended on stimulus termination asynchrony. Maximal masking occurred for target arcs as long as 5.0 deg of visual angle, exceeding previously reported distances. Misaligned or differently shaped stimuli produced less masking, suggesting that figural factors play a role in long-range backward masking.     

Understanding recovery from object substitution masking

When we look at a scene, we are conscious of only a small fraction of the available visual information at any given point in time. This raises profound questions regarding how information is selected, when awareness occurs, and the nature of the mechanisms underlying these processes. One tool that may be used to probe these issues is object-substitution masking (OSM). In OSM, a sparse, temporally-trailing four dot mask can interfere with target perception, even though the target and mask have different contours and do not spatially overlap (Enns & Di Lollo, 1997). Here, we investigate the mechanisms underlying the recently discovered recovery from OSM observed with prolonged mask exposure (Goodhew, Visser, Lipp, & Dux, 2011). In three experiments, we demonstrate that recovery is unaffected by mask offset, and that prolonged physical exposure of the mask is not necessary for recovery. These findings confirm that recovery is not due to: (a) an offset transient impairing the visibility of other stimuli that are nearby in space and time, or (b) mask adaptation or temporal object-individuation cues resulting from prolonged mask exposure. Instead, our results confirm recovery as a high-level visual-cognitive phenomenon, which is inherently tied to target-processing time. This reveals the prolonged iterative temporal dynamics of conscious object perception.     

Separating effects of orthographic similarity and contour summation in the identification of masked letter strings

We separated effects of contour summation and orthographic similarity under masking conditions, by comparing identification with simultaneous and sequentially presented letter strings, which either did or did not overlap spatially. With overlapping simultaneous stimuli, performance was better for strings with similar contours than for strings with the same letters (the orthographic similarity condition). This suggests that contour summation effects were strongest in the condition where stimuli had similar contours. With sequential presentations, performance in the similar contour and the orthographically similar conditions was equated when the stimuli were overlapping. However, effects of contour summation decreased when prime and target letters were spatially displaced, whereas performance in the orthographically similar condition was maintained. We conclude that effects of orthographic similarity can be distinguished from effects of contour summation, under masking conditions.     

Pathways in type-B (U-shaped) metacontrast

Rod and cone targets were crossed, in every combination, with rod and cone masks in flanking-bars metacontrast. Strong type-B (U-shaped) metacontrast was obtained in each condition, contrary to the claim that rod and cone masking are independent. In each condition, visibility declined steadily with stimulus-onset asynchrony (SOA) in trials in which target and mask appeared to be simultaneous, and increased with SOA in trials in which they appeared to be successive. The 'U' results from collapsing across these different types of trials, which may reflect distinct monotonic processes in masking. Under the light adaptation conditions used the time, Tmax, at which metacontrast was at a maximum was delayed by about 25 ms if rods, rather than cones, detected the target. Whether rods or cones detected the mask hardly altered Tmax.     

Variations in backward masking with different masking stimuli: II. The effects of spatially quantised masks in the light of local contour interaction, interchannel inhibition, perceptual retouch, and substitution theories

In part I we showed that with spatially non-overlapping targets and masks both local metacontrast-like interactions and attentional processes are involved in backward masking. In this second part we extend the strategy of varying the contents of masks to pattern masking where targets and masks overlap in space, in order to compare different masking theories. Images of human faces were backward-masked by three types of spatially quantised masks (the same faces as targets, faces different from targets, and Gaussian noise with power spectra typical for faces). Configural characteristics, rather than the spectral content of the mask, predicted the extent of masking at relatively long stimulus onset asynchronies (SOAs). This poses difficulties for the theory of transient-on-sustained inhibition as the principal mechanism of masking and also for local contour interaction being a decisive factor in pattern masking. The scale of quantisation had no effect on the masking capacity of noise masks and a strong effect on the capacity of different-face masks. Also, the decrease of configural masking with an increase in the coarseness of the quantisation of the mask highlights ambiguities inherent in the re-entrance-based substitution theory of masking. Different masking theories cannot solve the problems of masking separately. They should be combined in order to create a complex, yet comprehensible mode of interaction for the different mechanisms involved in visual backward masking.     

A comparison of masking by visual and transcranial magnetic stimulation: implications for the study of conscious and unconscious visual processing

Visual stimuli as well as transcranial magnetic stimulation (TMS) can be used: (1) to suppress the visibility of a target and (2) to recover the visibility of a target that has been suppressed by another mask. Both types of stimulation thus provide useful methods for studying the microgenesis of object perception. We first review evidence of similarities between the processes by which a TMS mask and a visual mask can either suppress the visibility of targets or recover such suppressed visibility. However, we then also point out a significant difference that has important implications for the study of the time course of unconscious and conscious visual information processing and for theoretical accounts of the processes involved. We present evidence and arguments showing: (a) that visual masking techniques, by revealing more detailed aspects of target masking and target recovery, support a theoretical approach to visual masking and visual perception that must take into account activities in two separate neural channels or processing streams and, as a corollary, (b) that at the current stage of methodological sophistication visual masks, by acting in more highly specifiable ways on these pathways, provide information about the microgenesis of form perception not available with TMS masks.     

Rapid enumeration within a fraction of a single glance: The role of visible persistence in object individuation capacity

The number of items that can be individuated at a single glance is limited. Here, we investigate object individuation at a higher temporal resolution, in fractions of a single glance. In two experiments involving object individuation we manipulated the duration of visual persistence of the target items with a forward masking procedure. The number of items as well as their stimulus–onset asynchrony (SOA) to the mask was varied independently. The results showed main effects of numerosity and SOA, as well as an interaction. These effects were not caused by a generic reduction of item visibility by the mask. Instead, the SOA manipulation appeared to fractionate the time to access the sensory image. These findings suggest that the capacity limit of 3–4 items found in object individuation is, at least partially, the consequence of the temporal window of access to sensory information.     

Metacontrast masking is processed before grapheme–color synesthesia

We investigated the physiological mechanism of grapheme–color synesthesia using metacontrast masking. A metacontrast target is rendered invisible by a mask that is delayed by about 60 ms; the target and mask do not overlap in space or time. Little masking occurs, however, if the target and mask are simultaneous. This effect must be cortical, because it can be obtained dichoptically. To compare the data for synesthetes and controls, we developed a metacontrast design in which nonsynesthete controls showed weaker dichromatic masking (i.e., the target and mask were in different colors) than monochromatic masking. We accomplished this with an equiluminant target, mask, and background for each observer. If synesthetic color affected metacontrast, synesthetes should show monochromatic masking more similar to the weak dichromatic masking among controls, because synesthetes could add their synesthetic color to the monochromatic condition. The target–mask pairs used for each synesthete were graphemes that elicited strong synesthetic colors. We found stronger monochromatic than dichromatic U-shaped metacontrast for both synesthetes and controls, with optimal masking at an asynchrony of 66 ms. The difference in performance between the monochromatic and dichromatic conditions in the synesthetes indicates that synesthesia occurs at a later processing stage than does metacontrast masking.     

Age differences in peripheral perceptual processing: a monoptic backward masking investigation

Peripheral processes in vision were investigated in two experiments involving monoptic backward masking with random noise. For young and old subjects, peripheral processing time (represented by stimulus onset asynchrony of target and mask) was characterized as a power function of target energy. Although processing time for both age groups showed a similar rate of decline with increasing target energy, old subjects processed targets more slowly at all energy levels. Results were independent of education, sex, and criterion differences between young and old. Target duration was related to critical interstimulus interval, such that stimulus onset asynchrony between target and mask was approximately constant for a given target energy within each age group. Evidence suggests that peripheral processing begins with target onset and that processing time is best characterized by a power function relating stimulus onset asynchrony of target and mask to target energy.     

Attention attenuates metacontrast masking

The influence of attention on perceptual awareness was examined using metacontrast masking. Attention was manipulated with endogenous cues to assess the effects on the temporal and spatial parameters of target visibility. Experiment 1 examined the time course of effective masking when the target and mask set were presented at an attended vs. an unattended location. The valid allocation of attention decreased the magnitude of the masking effect (i.e. increased visibility) for approximately 80 ms. Furthermore, even with spatial displacements of the target and mask and center-to-center separations of 1.5 degrees or 2.7 degrees of visual angle (Experiment 2), target visibility was increased when attention was validly allocated. These results indicate that attention influences low-level visual processes to enhance visual awareness.     

Individually different weighting of multiple processes underlies effects of metacontrast masking

Metacontrast masking occurs when a mask follows a target stimulus in close spatial proximity. Target visibility varies with stimulus onset asynchrony (SOA) between target and mask in individually different ways leading to different masking functions with corresponding phenomenological reports. We used individual differences to determine the processes that underlie metacontrast masking. We assessed individual masking functions in a masked target discrimination task using different masking conditions and applied factor-analytical techniques on measures of sensitivity. Results yielded two latent variables that (1) contribute to performance with short and long SOA, respectively, (2) relate to specific stimulus features, and (3) differentially correlate with specific subjective percepts. We propose that each latent variable reflects a specific process. Two additional processes may contribute to performance with short and long SOAs, respectively. Discrimination performance in metacontrast masking results from individually different weightings of two to four processes, each of which contributes to specific subjective percepts.     

Implicit semantic perception in object substitution masking

Decades of research on visual perception has uncovered many phenomena, such as binocular rivalry, backward masking, and the attentional blink, that reflect ‘failures of consciousness’. Although stimuli do not reach awareness in these paradigms, there is evidence that they nevertheless undergo semantic processing. Object substitution masking (OSM), however, appears to be the exception to this rule. In OSM, a temporally-trailing four-dot mask interferes with target perception, even though it has different contours from and does not spatially overlap with the target. Previous research suggests that OSM has an early locus, blocking the extraction of semantic information. Here, we refute this claim, showing implicit semantic perception in OSM using a target-mask priming paradigm. We conclude that semantic information suppressed via OSM can nevertheless guide behavior.     

The chronometry of mental ability: An event-related potential analysis of an auditory oddball discrimination task

The relation between intelligence and speed of auditory discrimination was investigated during an auditory oddball task with backward masking. In target discrimination conditions that varied in the interval between the target and the masking stimuli and in the tonal frequency of the target and masking stimuli, higher ability participants (HA) displayed more accurate discriminations, faster response time, larger P300 amplitude, and shorter P300 and mismatch negativity (MMN) latency than lower ability participants (LA). Task difficulty effects demonstrated with variation in mask type indicate that the mask does not interfere with the detection of the deviant target stimulus, but rather that the target and mask are integrated as a single compound stimulus. The temporal effects suggest that the speed of accessing short-term memory is faster for HA than LA and, on the basis of the MMN latency, the effect is accomplished automatically, without focused attention. Moreover, the pattern of results obtained with these data support the view that the accuracy effects are determined by processing speed rather than discrimination ability. Comparator models that accommodate these effects are discussed.     

An investigation into the representations involved in visual masking

Two experiments are reported in which the nature of the representations involved in visual masking with spatially overlapping stimuli is investigated. Recent work is described which was consistent with the proposal of Breitmeyer and Ganz (1976) that masking phenomena can be understood in terms of interactions between spatial-frequency-tuned channels. In the first experiment targets which had been filtered to contain only high or low spatial frequencies were masked by high or low frequency masks. The results were more consistent with a model of masking in which higher-order representations, possibly derived from spatial-frequency information, were involved. A second experiment was carried out to test this conjecture which involved investigating the interaction between the effects of learning and the type of information used in target identification. The results provided further support for the model.     

Spatial-frequency masking with briefly pulsed patterns

Spatial-frequency masking was studied with briefly pulsed (25 ms) vertical gratings. The mask was a noise grating, and the test pattern was a sinusoidal grating. A low-frequency band of noise masked a low- but not high-spatial-frequency test grating when the patterns were presented simultaneously. A high-frequency band of noise did not mask a low-frequency test grating when the patterns were presented simultaneously or when the mask was presented after the test pattern (backward masking). Masking was, however, observed when the mask or test pattern was of sufficiently high contrast so that the stimuli had nonlinear distortion and thus produced DC shifts of the field luminance.     

Target-mask shape congruence impacts the type of metacontrast masking

Visual metacontrast masking may depend on the time intervals between target and mask in two qualitatively different ways: in type-A masking the smaller the mask delay from target the stronger the masking while in type-B masking maximal masking effect is obtained with a larger temporal delay of the mask. Variability in the qualitative apperance of masking functions has been explained by variability in stimuli parameters and tasks. Recent research on metacontrast masking has surprisingly shown that both of these types of functions can be found with an identical range of stimulation parameters depending on individual differences between observers. Here we show that obtaining clear-cut type-A masking depends on whether target and mask shapes are congruent or incongruent and whether observers use the cues available due to the congruence factor. Conspicuously expressed type-A masking is selectively associated with incongruent target-mask pairings. In the latter conditions target identification level significantly drops with the shortest target-to-mask delays.     

Stream/bounce perception and the effect of depth cues in chimpanzees (Pan troglodytes)

The stream/bounce display represents an ambiguous motion event in which two identical visual objects move toward one another and the objects overlap completely before they pass each another. In our perception, they can be interpreted as either streaming past one another or bouncing off each other. Previous studies have shown that the streaming percept of the display is generic for humans, suggesting the inertial nature of the motion integration process. In this study, chimpanzees took part in behavioral experiments using an object-tracking task to reveal the characteristics of their stream/bounce perception. Chimpanzees did not show a tendency toward a dominant "stream" perception of the stream/bounce stimulus. However, depth cues, such as X-junctions and local motion coherence, did promote the stream percept in chimpanzees. These results suggest both similarities and differences between chimpanzees and humans with respect to motion integration and object individuation processes.     

Forward masking of faces by spatially quantized random and structured masks: On the roles of wholistic configuration, local features, and spatial-frequency spectra in perceptual identification

The forward masking of faces by spatially quantized masking images was studied. Masks were used in order to exert different types of degrading effects on the early representations in facial information processing. Three types of source images for masks were used: Same-face images (with regard to targets), different-face images, and random Gaussian noise that was spectrally similar to facial images. They were all spatially quantized over the same range of quantization values. Same-face masks had virtually no masking effect at any of the quantization values. Different-face masks had strong masking effects only with fine-scale quantization, but led to the same efficiency of recognition as in the same-face mask condition with the coarsest quantization. Moreover, compared with the noise-mask condition, coarsely quantized different-face masks led to a relatively facilitated level of recognition efficiency. The masking effect of the noise mask did not vary significantly with the coarseness of quantization. The results supported neither a local feature processing account, nor a generalized spatial-frequency processing account, but were consistent with the microgenetic configuration-processing theory of face recognition. Also, the suitability of a spatial quantization technique for image configuration processing research has been demonstrated.