Visual masking and the recovery phenomenon

Two experiments were carried out to investigate visual masking and target recovery. In the first experiment it was found that with superimposed disks of various sizes masking increases with increasing target-mask similarity and contour proximity. The results of the second study show that the extent of masking produced by a disk, which is slightly larger than the target, is drastically reduced when the mask in turn is followed by a ring, the inner contour of which is contiguous with the contour of the mask. This “facilitation effect” decreases as the interval between the mask and the third stimulus is increased. Target recovery in this situation appears to be brought about as a result of the reduction or elimination of the contour of the mask, which, as the first study has shown, is critical in bringing about the masking effect. The results are discussed in terms of some of the known physiological properties of the visual system.     

Dichotic backward masking of complex sounds

In the first experiment subjects identified a consonant-vowel syllable presented dichotically with a known contralateral masking sound at a stimulus onset asynchrony of ± 60 msec. When the mask followed the target syllable, perception of place of articulation of the consonant was impaired more when the mask was a different consonant-vowel syllable than when it was either a steady-state vowel or a non-speech timbre. Perception was disturbed less when the mask preceded the target, and the amount of disruption was independent of which mask was used. Greater backward than forward masking was also found in the second experiment for the identification of complex sounds which differed in an initial change in pitch. These experiments suggest that the extraction of complex auditory features from a target can be disrupted by the subsequent contralateral presentation of a sound sharing certain features with the target.     

Visual masking plays two roles in the attentional blink

When two targets are displayed in rapid visual sequence and masked by trailing patterns, identification accuracy is nearly perfect for the first target but follows a U-shaped pattern over temporal lag for the second target. Three experiments examined the role of visual masking in this attentional blink. Experiment 1 compared integration and interruption masks for both targets. Although either mask was effective in producing the blink when applied to the first target, only the interruption mask was effective when applied to the second target. Experiment 2 showed that integration masking of the second target was ineffective over a wide range of accuracy levels. Combining the two forms of masking in Experiment 3 confirmed the dissociation: A combined mask and only a main effect on accuracy for the first target, whereas it produced a qualitatively different pattern over temporal lag for the second target. These results suggest that representations of the target are substituted in consciousness by that of the interruption mask when visual attention is preoccupied.     

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.     

Quantitative theories of metacontrast masking

In metacontrast masking, the effect of a visual mask stimulus on the perceptual strength of a target stimulus varies with the stimulus-onset asynchrony (SOA) between them. As SOA increases, the target percept first becomes weaker, bottoms out at an intermediate SOA, and then increases for still larger SOAs. As a result, a plot of target percept strength against SOA produces a U-shaped masking curve. Theories have proposed special mechanisms to account for this curve, but new mathematical analyses indicate that it is a robust characteristic of a large class of neurally plausible systems. The author describes 3 quantitative methods of accounting for the U-shaped masking effect and analyzes 4 previously published mathematical models of masking. The models produce the masking curve through mask blocking, whereby a strong internal representation of the target blocks the mask's effects.     

Decoupling stimulus duration from brightness in metacontrast masking: data and models

A brief target that is visible when displayed alone can be rendered invisible by a trailing stimulus (metacontrast masking). It has been difficult to determine the temporal dynamics of masking to date because increments in stimulus duration have been invariably confounded with apparent brightness (Bloch's law). In the research reported here, stimulus luminance was adjusted to maintain constant brightness across all durations. Increasing target duration yielded classical U-shaped masking functions, whereas increasing mask duration yielded monotonic decreasing functions. These results are compared with predictions from 6 theoretical models, with the lateral inhibition model providing the best overall fit. It is tentatively suggested that different underlying mechanisms may mediate the U-shaped and monotonic functions obtained with increasing durations of target and mask, respectively.     

Inhibition and decay of motor and nonmotor priming

Motor responses can be facilitated by congruent visual stimuli and prolonged by incongruent visual stimuli that are made invisible by masking (direct motor priming). Recent studies on direct motor priming showed a reversal of these priming effects when a three-stimulus paradigm was used in which a prime was followed by a mask and a target stimulus was presented after a delay. A similar three-stimulus paradigm on nonmotor priming, however, showed no reversal of priming effects when the mask was used as a cue for processing of the following target stimulus (cue priming). Experiment 1 showed that the time interval between mask and target is crucial for the reversal of priming. Therefore, the time interval between mask and target was varied in three experiments to see whether cue priming is also subject to inhibition at a certain time interval. Cues indicated (1) the stimulus modality of the target stimulus, (2) the task to be performed on a multidimensional auditory stimulus, or (3) part of the motor response. Whereas direct motor priming showed the reversal of priming about 100 msec after mask presentation, cue priming effects simply decayed during the 300 msec after mask presentation. These findings provide boundary conditions for accounts of inverse priming effects.     

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.     

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.     

Recently attended masks are less effective

Much work has been done to investigate participants' ability to detect repeated targets, but the presentstudy examined the influence of recently attended stimuli on target masking. Participants performed a target identification task in which the item that masked the target was either a recently attended item or a novel item. When it was identical to a previously attended stimulus, the mask was rendered considerably less effective. We have termed this effect a repeated mask reduction (RMR). This simple manipulation resulted in a large, reliable effect on the efficacy of visual masking in a single-target identification paradigm. In Experiments 1, 2, and 3, we demonstrated the basic effect and noted that the RMR increased as task difficulty increased. Experiments 4 and 5 suggested that attention to the first instance of the mask was crucial to this effect by showing that the magnitude of the RMR was unaffected by repetition of nonmask distractors and that the magnitude of the effect was reduced when less attention was paid to the first instance of the mask.     

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.     

The roles of location specificity and masking mechanisms in the attentional blink

In a series of four experiments using rapid serial visual presentations of two target letters embedded in numeral distractors, with different numbers of display positions and with or without masking, we show that (1) the nonmonotonic, U-shaped attentional blink (AB) function, which occurs when all items are presented at the same display location, is eliminated in favor of a monotonic function when targets and distractors are presented randomly dispersed over four or nine adjacent positions; (2) the AB monotonicity is maintained with the spatially distributed presentation even when backward masks are used in all possible stimulus positions and when the location of the next item in sequence is predictable; and (3) the If-shaped AB is not due to position-specific forward or backward masking effects occurring at early levels of visual processing. We tentatively conclude that the U-shaped AB is primarily a function of the interruption of late visual processing produced when the item following the first target occurs at the same location. In order for the AB to severely disrupt performance, the item following the first target must be presented at the same location as the target so that it can serve both as a distractor and as a mask interrupting or interfering with subsequent visual processing.     

The roles of location specificity and masking mechanisms in the attentional blink.

In a series of four experiments using rapid serial visual presentations of two target letters embedded in numeral distractors, with different numbers of display positions and with or without masking, we show that (1) the nonmonotonic, U-shaped attentional blink (AB) function, which occurs when all items are presented at the same display location, is eliminated in favor of a monotonic function when targets and distractors are presented randomly dispersed over four or nine adjacent positions; (2) the AB monotonicity is maintained with the spatially distributed presentation even when backward masks are used in all possible stimulus positions and when the location of the next item in sequence is predictable; and (3) the U-shaped AB is not due to position-specific forward or backward masking effects occurring at early levels of visual processing. We tentatively conclude that the U-shaped AB is primarily a function of the interruption of late visual processing produced when the item following the first target occurs at the same location. In order for the AB to severely disrupt performance, the item following the first target must be presented at the same location as the target so that it can serve both as a distractor and as a mask interrupting of interfering with subsequent visual processing.     

On the role of object representations in substitution masking

Three experiments were conducted to investigate the role of object representations in object substitution masking (OSM). OSM occurs when a very sparse mask is presented simultaneously with a target stimulus and the target offsets first, leaving the mask to linger in the display for some time. Results confirm earlier claims that there is an isolatable object-level component to OSM and indicate that a target can be protected from OSM if, prior to offsetting, it can be represented as a distinct object from the mask. When the mask was presented as sliding past the target (Experiment 1), as jiggling independently of the target (Experiment 2), or in a different color from the target (Experiment 3), OSM was reduced or eliminated. This suggests that OSM reflects basic updating processes that allow the perception of continuity of object identity over change.     

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.     

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.     

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.     

Visual attention and the mechanism of metacontrast

The U-shaped metacontrast function may result from the superimposition of two monotonic components which reflect the effects of mechanisms similar to the peripheral and central processes suggested for backward pattern masking by Turvey (Psychol Rev 80:1–52, 1973). In an experiment using the disc-ring paradigm, it was demonstrated that the decreasing and increasing branches of the metacontrast function are differently affected by the exposure duration of the mask and a task-irrelevant stimulus (distractor) appearing in the contralateral visual hemifield. The phenomenal representation of masking is different for the two parts of the curve. It is suggested that masking in the second part of the masking function, but not in the first, is related to the control of visual attention.     

The joint effect of forward and backward visual masking: Some comments on Uttal’s “Character in the hole” experiment

The joint effect of forward and backward visual masking appears to be more extended in time than that predicted from an algebraic summation of individual forward and backward masking effects. It is suggested that this apparent extension of the temporal range of masking arises from the summation of forward and backward masking effects which in themselves are insufficient to influence observed performance. Such latent masking effects are possible if it is not assumed that when stimulus identification reaches the 100% level the mask has no effect at all on the stimulus.     

Testing quantitative models of backward masking

We analyzed the relationship between U-shaped and monotonic-shaped masking functions, using both computer simulations of quantitative models and experimental data. Our analysis revealed that quantitative models of backward masking predict that U-shaped masking functions should appear for weak masks and monotonic masking functions should appear for strong masks. The models predict, moreover, that for a fixed target and experimental task, as the mask changes it is possible to go from U-shaped to monotonic-shaped masking functions. Significantly, the models predict that at each stimulus onset asynchrony between the target and the mask, the U-shaped function must have weaker masking than the monotonic-shaped function. Contrary to the predictions of the models, we show an experimental situation that generates masking functions that violate this prediction.