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.     

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.     

Similarity effects in backward recognition masking

Auditory backward recognition masking refers to the ability of a masking sound to terminate further perceptual resolution of a test sound presented slightly earlier in time. The present experiments were conducted to determine whether mask/test tone similarity effects in backward recognition masking could be reliably demonstrated. Although similarity effects were found in Experiments 1 and 2, only about 60% of the subjects demonstrated these effects. Experiment 3 was designed to isolate which stage of information processing is responsible for similarity effects. It was hypothesized that similarity effects are due to mask interference with the synthesized auditory memory of the test tone rather than to selective overwriting of a preperceptual auditory store: previous research has shown that interference in synthesized auditory memory depends on the similarity of the interfering stimulus to the items held in memory. By independently varying the backward masking interval and the interfering effect of the mask on the test tone memory, it was possible to demonstrate that similarity effects are indeed caused by mask interference in synthesized memory. The implications of these results are considered in the framework of auditory and visual masking.     

Vibrotactile frequency recognition: forward and backward masking effects

Forward and backward vibrotactile recognition masking was investigated in 4 subjects with 240-Hz and 160-Hz targets of 20 ms duration and four 200-Hz masks, using interstimulus intervals (ISIs) ranging from -500 to 500 ms. Two of the masks (short) were 20 ms and two (long) were 200 ms in duration. One of each set of masks was matched in subjective intensity to the targets, but the others were more intense. The range of ISIs over which masking was obtained was comparable to that found by Massaro (1970) with auditory stimuli. Both short masks produced more masking than either long mask except at short ISIs. Larger mask intensities increased masking only at very short ISIs, and longer mask durations increased backward but not forward masking.     

Spatial factors in masking with black or white targets

Two masking experiments were carried out. In the first, duration thresholds were measured for a 10 min black test disc paired with a larger concentric black mask, ranging in size from 15 min to 2 deg. The stimuli were tachistoscopically presented centrally, or at 2 deg or 6 deg in the left binocular field. As mask diameter increased, test threshold decreased in a negatively accelerated function, which approached an asymptote below the unmasked condition. All functions are similar with systematic upward shifts for more peripheral stimulation. In Experiment 2, threshold luminance was adjusted for a 1 deg, 5-msec test flash paired with a 250-mseC., 34-mL mask, ranging from 1 deg to 6.2 deg in diameter. Stimuli were presented in Maxwellian view at 7.2 deg in the right eye nasal field. Results were similar to Experiment 1, except that the asymptote is significantly above the control condition. Both experimental results support a border inhibition hypothesis.     

The role of pattern goodness in the reproduction of backward masked patterns.

Four experiments investigated the role of pattern goodness in backward masking using five- and four-dot patterns constructed by placing dots in the cells of a 3 x 3 matrix. In Experiment 1, subjects rated the goodness of these patterns and the results replicated previous work showing that good patterns had few alternatives. In Experiment 2, the dot patterns were the target stimuli in a backward masking task using a variety of masking stimuli. For all masking, good patterns were reproduced more accurately than poor patterns. In Experiment 3, the goodness of the masking stimulus was varied. The results indicated that good patterns were reproduced more accurately (replicating Experiment 2) and that good patterns were less effective as stimulus than were poor patterns. In Experiment 4, a long interstimulus interval which precluded masking was used to determine whether goodness affected encoding or memory. At these intervals, there were no differences among patterns, suggesting that the effect of pattern goodness was on rate of encoding. These results demonstrate the importance of configural properties in pattern perception.     

Temporal characteristics of visibility in chimpanzees (Pan troglodytes) and humans (Homo sapiens) assessed by a visual-masking paradigm

We used the visual-masking paradigm to compare temporal characteristics of chimpanzee vision with those of humans. Two types of masking experiments were conducted. One type involved masking by noise, in which the visibility of the geometric pattern target was tested with a spatially overlapping noise as the mask stimulus. The other type involved paracontrast and metacontrast masking, in which the mask stimuli flanked but did not spatially overlap the target stimuli. Temporal characteristics regarding the visibility of target stimuli, displayed as functions of temporal asynchrony between target and mask stimuli, differed with the mask type in chimpanzees as in humans. Peak deterioration in visibility occurred at the point of minimum temporal asynchrony both in forward and backward masking by noise, but was not at 0 ms temporal asynchrony when the target and mask stimuli did not spatially overlap. These results suggest that chimpanzees and humans share the underlying mechanisms in two kinds of temporal inhibition caused by spatially overlapping and non-overlapping mask stimuli.     

Spatial frequency masking in positive- and negative-symptom schizophrenia

The role of transient and sustained channels in masking was investigated in groups with positive and negative symptoms in schizophrenia and in a control group. The target stimulus was a 3.0 c/deg sinusoidal grating, which was masked at 11 stimulus-onset asynchronies between -40 to 360 ms by a 1.0 c/deg mask or an 11.0 c/deg mask. The results showed that there was no difference between the control and positive-symptom groups in the perception of the 3 c/deg target stimulus, nor was there a difference when the target was masked by 1 or 11 c/deg masking stimuli. In comparison with the control and positive-symptom groups, the negative-symptom group showed a significantly higher threshold for the perception of the 3 c/deg target stimulus and more masking with a 1 c/deg mask, but not with an 11 c/deg mask. The results provide evidence for distinguishable differences in visual masking between groups with positive and negative symptoms in schizophrenia.     

Sounds change four-dot masking

The temporal occurrence of a flash can be shifted towards a slightly offset sound (temporal ventriloquism). Here we examined whether four-dot masking is affected by this phenomenon. In Experiment 1, we demonstrate that there is release from four-dot masking if two sounds - one before the target and one after the mask - are presented at ∼100 ms intervals rather than at ∼0 ms intervals or a silent condition. In Experiment 2, we show that the release from masking originates from an alerting effect of the first sound, and a temporal ventriloquist effect from the first and second sounds that lengthened the perceived interval between target and mask, thereby leaving more time for the target to consolidate. Results thus show that sounds penetrate the visual system at more than one level.     

A recognition masking study of consonant processing

The processing of consonants was investigated in a series of experiments using a recognition masking paradigm. Experiment I investigated the effects of target duration, interstimulus interval, forward vs. backward masking, and the phonetic feature composition of the target and mask on accuracy of target identification. Experiment II assessed consonant processing when the target and mask were presented dichotically in order to separate central and peripheral components of consonant masking. Experiment III investigated the effects of mask duration on consonant processing. Substantial masking was found in backward and forward diotic and dichotic conditions. Evidence for target-mask interaction at the level of phonetic features was also found.     

Two visual stores and two processing operations in tachistoscopic partial report

A two-stage interpretation of the processes underlying tachistoscopic partial report performance is suggested. It is assumed that partial report is mediated by two kinds of visual store (a sensory store and a short-term store) and by two processing operations (selection and naming). In Experiment I, the accuracy and latency of two types of partial report (report by location and report by colour) were compared for cue stimulus-test stimulus intervals ranging from --500 ms to + 500 ms. It was concluded that selection by colour takes longer than selection by location; an explanation in terms of differential decay of attributes in the sensory store was rejected. In Experiment II, cue stimulus delays of 0, 150 and 300 ms were employed, and a backward masking stimulus followed the cue stimulus with a delay of 200, 300, 400 or 600 ms. The amount of masking depended on the cue stimulus-masking stimulus interval, rather than on the test stimulus-masking stimulus interval. It was concluded that selection operates on the sensory store and that backward masking can affect the naming of a stimulus representation which is residing in the visual short-term store.     

An attentional mechanism in the analysis of spatial frequency

Sinusoidal gratings of various spatial frequencies were used as masking stimuli in a detection task and a vernier acuity task. The test stimuli were 1 cycle/deg square-wave gratings. The spatial frequency of the most effective mask was 1 cycle/deg for the detection task but 3 cycles/deg for the vernier acuity task. The different masking functions for the two tasks show that the visual system analyzes the square-wave stimulus into its various spatial-frequency components. Since the test stimulus was the same for both tasks, the different masking functions may be the result of an attentional mechanism that weighs the importance of the output from various spatial-frequency analyzers. Whether the information from a particular spatial-frequency analyzer is attended or not depends upon the task the visual system must perform.     

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.     

Vowel recognition: Inferences from studies of forward and backward masking

The recognition of brief vowels was studied in forward and backward masking tasks. In a series of experiments in which both target and mask parameters were systematically varied, two populations of subjects were identified. The majority (Nonmaskers) evidenced little masking at any interstimulus interval, while relatively fewer subjects (Maskers) evidenced backward masking (but not forward masking) over a 100-200 ms interval. Increasing target set size systematically increased masking for the Maskers but not for the Nonmaskers. Adding white noise to the targets increased the extent of masking for both groups. These results suggest (1) that masking does not impose a substantive constraint on vowel perception in running speech, and (2) that multiple strategies may exist for vowel recognition.     

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.     

The role of edge-based and surface-based information in natural scene categorization: Evidence from behavior and event-related potentials

A fundamental question in vision research is whether visual recognition is determined by edge-based information (e.g., edge, line, and conjunction) or surface-based information (e.g., color, brightness, and texture). To investigate this question, we manipulated the stimulus onset asynchrony (SOA) between the scene and the mask in a backward masking task of natural scene categorization. The behavioral results showed that correct classification was higher for line-drawings than for color photographs when the SOA was 13 ms, but lower when the SOA was longer. The ERP results revealed that most latencies of early components were shorter for the line-drawings than for the color photographs, and the latencies gradually increased with the SOA for the color photographs but not for the line-drawings. The results provide new evidence that edge-based information is the primary determinant of natural scene categorization, receiving priority processing; by contrast, surface information takes longer to facilitate natural scene categorization.     

Effects of partial symmetry, exposure time, and backward masking on judged goodness and reproduction of visual patterns

Six experiments investigated the effects of partial symmetry in visual patterns on judgement of pattern goodness, immediate memory, and learning. In Experiments 1—III pattern goodness ratings were substantially inter-correlated among a self-paced test condition and two conditions producing moderate to severe stimulus degradation (brief tachistoscopic exposure, and backward masking): the less the partial symmetry in a pattern, the lower was the judged goodness of the pattern. In Experiments IV and V immediate reproduction of patterns was observed respectively following exposures of 5-5000 ms, and backward masking. Correct reproduction improved with degree of partial symmetry. Concordant results were found in a free recall learning task (Experiment VI). Correlations between goodness and learning and memory performance for discrete patterns were always substantial. The results strongly suggest that pattern goodness can be appraised reliably and accurately with information processing times too short to permit pattern encoding in short-term visual memory. Evaluation of pattern goodness must therefore rest upon early (precategorical) processing of symmetry features.     

Temporal aspects of selective masking

In two experiments, rows of random letter sequences were presented for 100 ms and were patterned masked at varying delays after display offset. In Experiment I recall was probed by visual partial report cues, while auditory probes were employed in Experiment II. Compared to no-masking control conditions, the masking stimulus had a selective effect at the different positions of the rows. The masking stimulus produced the largest decrements in recall of letters from the centre positions of the displays but had a minimal effect on performance at either end of the rows. Furthermore, it was demonstrated that improvements in recall were limited to the centre positions of the rows at increased delays of mask. Subsidiary analyses revealed that processing of the end letters of the displays terminates shortly after display offset while processing of the centre letters continues for at least 500 ms. The results are consistent with the notion that processing of multi-letter arrays commences at the ends of the rows and that the selective masking effect reflects the order of processing of the contents of iconic memory. However, these results were evident only in Experiment II which employed auditory partial report cues. When the partial report cues were visual, there were no effects of masking and minimal increases in performance at increased delays of mask. The discrepant results of the two experiments are discussed in terms of process interruption caused by obligatory attention to the partial report cues.