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.     

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.     

Individual differences in metacontrast masking are enhanced by perceptual learning

In vision research metacontrast masking is a widely used technique to reduce the visibility of a stimulus. Typically, studies attempt to reveal general principles that apply to a large majority of participants and tend to omit possible individual differences. The neural plasticity of the visual system, however, entails the potential capability for individual differences in the way observers perform perceptual tasks. We report a case of perceptual learning in a metacontrast masking task that leads to the enhancement of two types of adult human observers despite identical learning conditions. In a priming task both types of observers exhibited the same priming effects, which were insensitive to learning. Findings suggest that visual processing of target stimuli in the metacontrast masking task is based on neural levels with sufficient plasticity to enable the development of two types of observers, which do not contribute to processing of target stimuli in the priming task.     

The electrophysiological correlates of stimulus visibility and metacontrast masking

There are conflicting views concerning the electrophysiological correlates of visual consciousness. Whereas one view considers a relatively late positive deflection (LP) as a primary correlate of consciousness, another model links consciousness with earlier negativity (VAN). The present experiment utilized metacontrast masking in investigating the electrophysiological correlates of visual consciousness. The participants were presented with target-mask sequences in three stimulus onset asynchronies. The target stimuli were followed by either a metacontrast mask or a similar-looking, but ineffective pseudomask. The results showed that the first deflection that correlated with target visibility was VAN which was followed by LP. We argue that the VAN is the primary correlate target visibility, while the LP reflects later, postperceptual processing stages.     

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.     

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.     

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.     

Attend to it now or lose it forever: selective attention,metacontrast masking,and object substitution

Metacontrast masking occurs when the visibility of a brief target stimulus is decreased by the subsequent appearance of another nearby visual stimulus. Early explanations of the phenomenon involved low-level mechanisms, but subsequent studies have suggested a role for selective attention. The results of three experiments presented here extend previous findings to the metacontrast paradigm. It is shown that the strength of metacontrast masking increases with the number of distractor items in a display, decreases when the target location is validly but not invalidly precued, and is eliminated when search for the target is efficient (pop-out search) but not when search is inefficient (serial search). A connection between metacontrast masking and object substitution masking is considered.     

Decrease in metacontrast masking following adaptation to flicker

Selective adaptation was used to explore the characterisitcs of a metacontrast masking stimulus which contribute to its effectiveness in masking the test stimulus. Subjects adapted for 10 s to a configuration like the masking stimulus that was either continuously on or flickering. Following this they viewed a metacontrast presentation and estimated the brightness of the test stimulus. Prior adaptation to a continuously present stimulus did not appreciably affect metacontrast masking; however, masking was greatly reduced following adaptation to flickering stimuli. These results are consistent with recent models of metacontrast masking based on transient and sustained visual channels.     

The effects of complexity on the perception of vibrotactile patterns

Vibrotactile patterns were presented to subjects’ left index fmgerpads using the array from the Optacon. A set of simple (one-line) patterns and a set of complex (two-line) patterns were constructed so that they were equally identifiable when presented individually. In Experiment 1, discrimination performance was lower for two-line patterns than for one-line patterns. Communality, the number of lines that two patterns share in common, appeared to be the major factor in reducing discrimination performance for two-line patterns. Experiment 2 measured the time required to identify individual patterns. There was no significant difference in identification times for one- and two-line patterns, suggesting that features within a pattern were processed simultaneously. In the presence of a temporal masking stimulus (Experiment 3), two-line patterns were more difficult to identify than one-line patterns, but reaction times were similar for the two sets of patterns. The results suggest that varying complexity affects perception of patterns at later stages of processing.     

Masking procedures can influence priming effects besides their effects on conscious perception

Masked priming has been employed to study the role of consciousness for different levels of visual processing. However, masking procedures differ systematically between studies. To examine these procedural differences we contrasted priming effects with metacontrast masking, which is often applied in the context of perceptual priming, and priming effects with sandwich pattern masking, frequently used in studies on semantic priming. Results indicate that the amount of masking neither affects perceptual nor semantic priming effects in a semantic categorization task when a metacontrast masking paradigm was used. However, perceptual and semantic priming effects increased with increasing prime visibility when a sandwich pattern masking paradigm was used. Findings suggest that different types of masking procedures affect the processing of the masked stimuli in substantially different ways even if the masking effect on conscious perception of these stimuli is comparable.     

Temporal integration and vibrotactile backward masking

Subjects were presented with vibrotactile target patterns to their left index fingertips. The target patterns varied in the number of line segments that they contained and were presented in the presence or absence of a backward-masking stimulus. The stimulus onset asynchrony (SOA) between the target and masker was varied. In an identification task, subjects' errors indicated that the effect of the masker at brief SOAs was to increase the perceived number of line segments in the target. This effect diminished with increasing SOA, and at the longest SOAs subjects confused targets with patterns containing the same number of line segments but varying in how the line segments were related. In an estimation task, the effect of the masker was to increase the number of line segments estimated to be contained in the target pattern. The effect of the masker at brief SOAs is discussed in terms of an integration theory of vibrotactile backward masking. At longer SOAs, the results suggest that the masker may interfere with the extraction of relational information in the target pattern.     

Attention capture by contour onsets and offsets: No special role for onsets

In five experiments, we investigated the power of targets defined by the onset or offset of one of an object’s parts (contour onsets and offsets) either to guide or to capture visual attention. In Experiment 1, search for a single contour onset target was compared with search for a single contour offset target against a static background of distractors; no difference was found between the efficiency with which each could be detected. In Experiment 2, onsets and offsets were compared for automatic attention capture, when both occurred simultaneously. Unlike in previous studies, the effects of overall luminance change, new-object creation, and number of onset and offset items were controlled. It was found that contour onset and offset items captured attention equally well. However, display size effects on both target types were also apparent. Such effects may have been due to competition for selection between multiple onset and offset stimuli. In Experiments 3 and 4, single onset and offset stimuli were presented simultaneously and pitted directly against one another among a background of static distractors. In Experiment 3, we examined “guided search,” for a target that was formed either from an onset or from an offset among static items. In Experiment 4, the onsets and offsets were uncorrelated with the target location. Similar results occurred in both experiments: target onsets and offsets were detected more efficiently than static stimuli which needed serial search; there remained effects of display size on performance; but there was still no advantage for onsets. In Experiment 5, we examined automatic attention capture by single onset and offset stimuli presented individually among static distractors. Again, there was no advantage for onset over offset targets and a display size effect was also present. These results suggest that, both in isolation and in competition, onsets that do not form new objects neither guide nor gain automatic attention more efficiently than offsets. In addition, in contrast to previous studies in which onsets formed new objects, contour onsets and offsets did not reliably capture attention automatically.     

The effects of onset and offset warning and post-target stimuli on the saccade latency of children and adults

Two studies, involving children (mean age = 10 years) and adults, investigated the effects of visual stimulus onsets and offsets on the latency of saccades to peripheral targets. Saccade latency was reduced when foveal stimulus onsets or offsets preceded the target. When stimulus onset occurred 100 msec after target onset, the stimulus interfered with responding, with this interference effect significantly greater for children than for adults. When stimuli were presented in the peripheral visual field facilitation and interference effects were similar for children and adults. These results were interpreted as indicating that oculomotor processes are similar in children and adults while the stimulus intake processes that follow stimulus onset at the point of fixation have a greater interference effect on children's than on adults' eye movements.     

Exogenous spatial precuing reliably modulates object processing but not object substitution masking

Object substitution masking (OSM) is used in behavioral and imaging studies to investigate processes associated with the formation of a conscious percept. Reportedly, OSM occurs only when visual attention is diffusely spread over a search display or focused away from the target location. Indeed, the presumed role of spatial attention is central to theoretical accounts of OSM and of visual processing more generally (Di Lollo, Enns, & Rensink, Journal of Experimental Psychology: General 129:481–507, 2000). We report a series of five experiments in which valid spatial precuing is shown to enhance the ability of participants to accurately report a target but, in most cases, without affecting OSM. In only one experiment (Experiment 5) was a significant effect of precuing observed on masking. This is in contrast to the reliable effect shown across all five experiments in which precuing improved overall performance. The results are convergent with recent findings from Argyropoulos, Gellatly, and Pilling (Journal of Experimental Psychology: Human Perception and Performance 39:646–661, 2013), which show that OSM is independent of the number of distractor items in a display. Our results demonstrate that OSM can operate independently of focal attention. Previous claims of the strong interrelationship between OSM and spatial attention are likely to have arisen from ceiling or floor artifacts that restricted measurable performance.     

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.     

Modulation of oculomotor capture by abrupt onsets during attentionally demanding visual search

The influence of abrupt onsets on attentionally demanding visual search (i.e., search for a letter target among heterogeneous letter distractors), as indexed by performance and eye movement measures, was investigated in a series of studies. In Experiments 1 and 2 we examined whether onsets would capture the eyes when the appearance of an onset predicted neither the location nor the identity of the target. Subjects did direct their eyes to the abrupt onsets on a disproportionate number of trials in these studies. Interestingly, however, onset capture was modulated by subjects' scan strategies. Furthermore, onsets captured the eyes less frequently than would have been predicted by paradigms showing attentional capture when no eye movements are required. Experiment 3 examined the question of whether onsets would capture the eyes in a situation in which they never served as the target. Capture was observed in this study. However, the magnitude of capture effects was substantially diminished as compared to previous behavioural studies in which the onset had a chance probability of serving as the target. These data are discussed in terms of the influence of top-down constraints on stimulus-driven attentional and oculomotor capture by abrupt onset stimuli.     

W-shaped and U-shaped functions obtained for monoptic and dichoptic disk-disk masking

For nonmetacontrast (disk-disk) masking, if the outer diameter of the mask equals that of an annulus which produces typical metacontrast functions, U- and W-shaped functions will be obtained if (1) the stimuli are viewed dichoptically and monoptically, respectively. and (2) the mask is no more than about 10 times the energy (luminance x duration) of the target. As this energy ratio is approached, both types of functions become monotonic. These shapes suggest that interactions at different visual-pathway loci may he mapped by visual masking functions.     

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.     

OBJECT SUBSTITUTION:

Abstract —Can four dots that surround, but do not touch, a target shape act as a mask to reduce target discriminability? Although existing theories of metacontrast and pattern masking say "no." we report this occurs when targets appear in unpredictable locations. In three experiments, a four-dot mask was compared with a standard metacontrast mask that surrounded the target. Although accuracy was predictably different for the two masks at a central display location in Experiment I. both masks had similar strong effects on accuracy in parafoveal locations. Experiment 2 revealed that both four-dot and metacontrast masking were insensitive to contour proximity in parafoveal display locations, and Experiment 3 showed that four-dot masking could occur even at a central location if attention was distributed among several targets. We propose that targets in unattended locations are coded with low spotiotemporal resolution, leaving them vulnerable to substitution by the four dots when attention is directed to them.