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.     

Vibrotactile masking: A comparison of energy and pattern maskers

Subjects were required to identify vibrotactile patterns presented to their fingertips. The patterns, letters of the alphabet, were presented singly or in the presence of other vibrotactile masking stimuli. Two types of masking stimuli were used: an energy masker and a pattern masker. The effectiveness of these two types of maskers in interfering with letter recognition was tested, using them as forward and as backward maskers and presenting them at several different levels of intensity. The results showed more masking by the pattern masker, more backward than forward masking, and more masking as intensity increased. In addition, compared with the energy masker, the pattern masker showed both a greater difference between forward and backward masking and a greater increase in masking as masker intensity increased. The results are discussed in terms of a two-factor model of vibrotactfle masking.     

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.     

Masking of and by tactile pressure stimuli

Masking of and by tactile pressure stimuli was investigated in six Ss as a function of stimulus intensity (force) and stimulus onset asynchrony. Increase in the force of the masked stimulus and decrease in the force of the masking stimulus were inversely related to the magnitude of masking, as defined by either a relative or an absolute decrease in sensitivity. The introduction of stimulus onset asynchrony produced both forward and backward masking, the latter being of somewhat larger magnitude. Comparisons are made with results obtained in visual metacontrast masking.     

Intelligence and information processing during an auditory discrimination task with backward masking: an event-related potential analysis

The relation between mental ability and auditory discrimination ability was examined by recording event-related potentials from 60 women during an auditory oddball task with backward masking. Across conditions that varied in intensity and in the interval between the target and masking stimuli, the higher ability (HA) group exhibited greater response accuracy, shorter response times, larger P3 amplitude, and shorter P3 latency to target stimuli than the lower ability (LA) group. When instructed to ignore the stimuli, the HA group exhibited shorter mismatch negativity latency to deviant tones than the LA group. The greater speed and accuracy of auditory discrimination for the HA group, observed here with multiple measures, is not a consequence of response strategy, test-taking ability, or attention deployment.     

Backward and forward masking in the perception of cutaneous stimuli

Masking of the perception of an electrical test stimulus by a mechanical shock was studied in six Ss. Forward and backward masking were observed in all Ss, the former being of longer duration. Duration of the masking effects is inversely related to the intensity of the test stimulus. Masking effects may be preceded and followed by perceptual facilitation. The masking effects may be responsible for the alterations in the perception of a somaesthetic stimulus before and during movement of the stimulated area.     

Vibrotactile difference thresholds for intensity and the effect of a masking stimulus

Vibrotactile difference thresholds for intensity were measured at several intensity levels of a test stimulus in the absence of a masking vibration and in the presence of three different amplitudes of a masking vibration. The test stimulus was a 160-Hz vibration delivered to the right index finger. The masking stimulus was a 160-Hz vibration delivered to the right little finger. For the same amplitudes of the test stimulus, △I varied as a direct function of the amplitude of the masking vibration. The smallest △Is resulted from measurements made in the absence of the masking stimulus. The Weber fraction, △I/I, was constant only for the more intense test stimuli in the absence of any masking stimuli. Independent of the presence or level of the masker, the Weber fraction for all stimuli approached approximately the same value, .25, when the test stimuli were raised to 20-dB sensation level. A model is proposed to account for the increase in the Weber fraction as a function of masker intensity and to predict masked thresholds.     

U-shaped backward contour masking during stroboscopic motion.

Two stationary and spatially separated visual stimuli, presented briefly and successively in time, are known to produce stroboscopic motion whose vividness is a U-shaped function of the stimulus onset asynchrony. Contour masking is also known to occur under such stimulus conditions. The findings show that the contour masking is confined to only the first stimulus and that it, like metacontrast, is a backward U-shaped function of the stimulus onset asynchrony. A simple model, based on known psychophysical and neurophysiological properties, is proposed to explain these results.     

Interaction of forward and backward visual masking

An investigation was conducted into the interaction of the forward and backward masking effects of unpatterned visual stimuli. It was found that detection of a test spot was easier under conditions that should have provided both forward and backward masking than under either forward masking or backward masking alone. The implications for an integration theory of masking are discussed, and the findings are contrasted with findings on the interaction of forward and backward masking by dynamic visual noise.     

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.     

Backward and forward masking associated with saccadic eye movement

Visual masking effects on test flash thresholds were measured under real and simulated eye movement conditions to determine whether visual masking is primarily responsible for elevations in threshold that are sometimes associated with saccadic eye movements. Brief luminous flashes presented to the central retina before, during, and after saccades were masked by stimuli presented either pre- or postsaccadically. The amount and time course of masking were quantitatively dependent on stimulus parameters of intensity and temporal separation and were unaffected by eye movement parameters (amplitude, velocity, direction) as long as retinal stimulus conditions were constant. The duration of forward masking was longer than that of backward masking. When retinal conditions during saccades were mimicked while the eyes were held steady, masking interactions were identical to those obtained during real saccades. These results indicate that masking effects during saccades in ordinary environments are determined solely by the stimulus situation at the retina. Putative nonvisual, centrally originating saccadic suppression suggested by other authors is evidently not additive with visually determined masking during saccades.     

TMS effects on subjective and objective measures of vision: stimulation intensity and pre- versus post-stimulus masking

Transcranial magnetic stimulation (TMS) can be used to mask visual stimuli, disrupting visual task performance or preventing visual awareness. While TMS masking studies generally fix stimulation intensity, we hypothesized that varying the intensity of TMS pulses in a masking paradigm might inform several ongoing debates concerning TMS disruption of vision as measured subjectively versus objectively, and pre-stimulus (forward) versus post-stimulus (backward) TMS masking. We here show that both pre-stimulus TMS pulses and post-stimulus TMS pulses could strongly mask visual stimuli. We found no dissociations between TMS effects on the subjective and objective measures of vision for any masking window or intensity, ruling out the option that TMS intensity levels determine whether dissociations between subjective and objective vision are obtained. For the post-stimulus time window particularly, we suggest that these data provide new constraints for (e.g. recurrent) models of vision and visual awareness. Finally, our data are in line with the idea that pre-stimulus masking operates differently from conventional post-stimulus masking.     

The effects of graphemic and phonemic similarity between targets and masks in a backward visual masking paradigm

Experiments using a backward visual masking technique are described, in which the second (mask) stimulus is itself masked by a third stimulus, thus rendering guessing strategies, about target/mask relationships, difficult for subjects. Word-word and word-non-word sequences are used for the first two stimuli and it is shown that when the second stimulus resembles the first, either physically or phonologically, the severity of masking of the first is reduced. However, the target is not better reported when the mask word is semantically related to it. Consideration is given to the levels at which interaction between target and mask might occur.     

Tactile selective attention and temporal masking

The presentation of a nontarget stimulus to one fingerpad interferes with the identification of a target stimulus presented to a second fingerpad. This interference has been attributed to a failure of selective attention and, more specifically, to the nontarget’s eliciting a competing response. In the present study, the temporal interval between the target and nontarget was varied to determine the extent to which a nontarget primes a competing response. The results showed more interference when the nontarget was presented after the target than when it was presented before the target. Although still consistent with a response-competition explanation, this result offered no support for a priming explanation. The function relating the amount of interference to the temporal separation between the target and nontarget was similar to the functions obtained in studies of temporal masking, and this prompted a second experiment in which temporal masking was examined. These results, obtained with stimuli presented to the same fingerpad, indicate that response competition may be a major factor in temporal masking and that similar processes are involved in temporal masking and selective attention.     

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.     

Laterality differences and practice effects under central backward masking conditions

Two experiments were conducted to examine laterality differences and practice effects under various central backward masking conditions. Critical stimulus onset asynchrony (SOA) was determined for subjects on 3 consecutive days using single letters as target stimuli (TS) and a pattern masking stimulus (MS). There was a right visual field (RVF) advantage on Day 1 but no difference between the visual fields on following days. The decline in the RVF advantage appeared to be dependent upon prior experience with laterally located letters, to be independent of initial experience with a particular set of letters, and to be more pronounced for females than for males. In addition, large improvements in performance were found, particularly between the first and second testing sessions. These practice effects were discussed in terms of the possible development of strategies for enhancing TS features or attenuating MS features.     

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.     

Visual backward masking as measured by voice reaction time

Instead of using percent correct identifications or detections as the dependent variable, latency in voicing the target stimulus was measured in a backward masking paradigm. Reaction time (RT) to target letters was reliably increased when they were simultaneously encircled by a black ring mask of a size found to produce masking using an identification or detection criterion. The masking function in terms of RT was typical in shape, a decreasing function of stimulus onset asynchrony (SOA) over an interval of 150 msec. Since the target remained “on” when the mask appeared, the results are incompatible with an erasure interpretation of masking effects. Analyses of the variances of the RTs supported an interpretation of a progressive decrease in masking effects as SOA increased.     

Variations in backward masking with different masking stimuli: I. Local interaction versus attentional switch

The types of stimuli used as targets and masks considerably change the masking functions in a way that requires us to abandon any single mechanism of masking as the sole explanation of backward masking. In the first of two reports in which the problem of the mask-dependence of masking is addressed, we explore the role of the relative spatial positioning of targets and masks in order to differentiate between local interaction and attentional models. If single letters were masked by double-letter masks then the relative spatial arrangement of the letters, which was changed in order to vary the involvement of metacontrast-like processes, had an effect at shorter SOAs, but not at longer SOAs where strong masking still persisted. This poses difficulties for proposing local contour interaction as the main mechanism of masking. Similarly, crowding effects alone cannot explain the results. Backward masking also involves attention being directed to working-memory processing of the succeeding object while abandoning the preceding object.     

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.