Parallel but temporally displaced visual half-field metacontrast functions

Using a classic letter-ring metacontrast paradigm, left and right visual field meta-contrast functions were separately determined. The parallel U-shaped recognition functions for both half-fields were found to interact differentially with stimulus onset asynchrony, the left visual field function being displaced by 13 ms toward longer test stimulus-masking stimulus separations. This result was consistent with the hypothesis of longer processing time requirements for verbal stimuli delivered to the right than to the left hemisphere. This indicates that the neural locus (loci) responsible for left visual field verbal processing delay is (are) capable of mediating metacontrast phenomena. It was tentatively concluded that a relative processing delay within the right hemisphere underlies the differing visual half-field metacontrast interaction with stimulus onset asynchrony.     

A tactile metacontrast effect

Vibrotactile patterns, generated on the 6×24 array of the Optacon, were presented to subjects’ left index fingertips. The subjects identified these patterns in the absence of any masking stimuli and in the presence of spatially adjacent masking stimuli. The amount of interference in recognizing the patterns was measured as a function of the interval between target and masker onsets. Masking functions similar to those reported in visual metacontrast studies were found; that is, more masking occurred when masker onset followed target onset by 25 to 50 msec than when onsets were simultaneous. Subjects showed more metacontrast when masker energy was reduced, a finding paralleled in the visual literature. The relevance of some models of visual metacontrast to the tactile findings is discussed.     

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.     

An onset-onset law for one case of apparent motion and metacontrast

Ss rated the quality of apparent motion and of metacontrast in computer-controlled sequences of two or of three outlined squares. For brief stimuli, the dependence of the two effects on temporal factors of stimulation is virtually identical. Motion and metacontrast depend solely on the asynchrony of onsets between the two exposures (SOA) over a wide range of duration and interstimulus intervals (lSI). Metacontrast suppression is interpreted as a case of impossible motion. The temporal determinants of apparent motion are summarized in a model in which the effect occurs when the temporal overlap between the perceptual responses to the successive stimuli is intermediate in value.     

Foveal metacontrast: I. Criterion content and practice effects

Strong metacontrast was found during experiments involving foveal presentation of stimuli. Follow-up experiments indicate that foveal metacontrast can be accounted for in some conditions by a practice effect and/or a criterion-content change, which occurs with practice and involves a biphasic brightness response to the target. Consideration of these factors may help resolve some of the many apparent disparities in the metacontrast literature. The relevance of these factors to metacontrast theories is discussed.     

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.     

Gamma神经振荡和信息整合加工

Gamma神经振荡是一种基础神经活动。它的特性使其与“信息整合加工”产生了潜在联系。已有研究显示, 自下而上的跨通道信息整合与感觉皮层的Gamma振荡同步化有关; 单通道自上而下的信息整合与高级皮层的Gamma振荡增强有关。现有的“神经耦合理论”和“匹配利用模型”分别描述了Gamma振荡如何在“自下而上”及“自上而下”的信息整合中发挥作用。Gamma振荡虽与整合加工密切相关, 但作为指标需谨慎。对于Gamma振荡在复杂情景整合加工中的作用仍待探究。     

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.     

Effects of stimulus order on discrimination processes in comparative and equality judgements: Data and models

In typical discrimination experiments, participants are presented with a constant standard and a variable comparison stimulus and their task is to judge which of these two stimuli is larger (comparative judgement). In these experiments, discrimination sensitivity depends on the temporal order of these stimuli (Type B effect) and is usually higher when the standard precedes rather than follows the comparison. Here, we outline how two models of stimulus discrimination can account for the Type B effect, namely the weighted difference model (or basic Sensation Weighting model) and the Internal Reference Model. For both models, the predicted psychometric functions for comparative judgements as well as for equality judgements, in which participants indicate whether they perceived the two stimuli to be equal or not equal, are derived and it is shown that the models also predict a Type B effect for equality judgements. In the empirical part, the models' predictions are evaluated. To this end, participants performed a duration discrimination task with comparative judgements and with equality judgements. In line with the models' predictions, a Type B effect was observed for both judgement types. In addition, a time-order error, as indicated by shifts of the psychometric functions, and differences in response times were observed only for the equality judgement. Since both models entail distinct additional predictions, it seems worthwhile for future research to unite the two models into one conceptual framework.     

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.     

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.     

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.     

Perceptual delay: a consequence of metacontrast and apparent motion

Temporal-order judgments were used to demonstrate that a later visual stimulus can delay the perception of an earlier one when the two stimuli together produce the phenomenon of metacontrast or of apparent motion. The perceptual delay is the same for movement and metacontrast and for one or two characters appearing to move or to be masked.     

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.     

Perception: a model comprising two modes of consciousness

A model of human perception is proposed in which conscious awareness is assumed to be the result of two separate mechanisms each involving consciousness, one outer, sensori-produced, and one inner, conceptual. By mediation of flexible memory representations the sensory data of the outer consciousness give rise to a matched "copy" in the inner consciousness which conceptually organizes the former and also serves as input to the memory store. The model is applied to some perceptual problems in vision such as ambiguous stimuli, subjective contours, space perception, a case of metacontrast, and subliminal perception.     

Spatial factors in metacontrast

Different mask ring widths, intercontour distances, mask durations, and interstimulus intervals were varied in a parametric manner. Results show decreasing amounts of metacontrast with increases in intercontour distance, and no significant effects of mask width or mask duration. The results provide support for monotonic metacontrast functions with maximum metacontrast at the offset of the target.     

Apparent movement and metacontrast: A note on Kahneman’s formulation

Recently metacontrast has been described as a case of “impossible” apparent motion. Kahneman (J 967) has supported this hypothesis with a study showing that apparent motion and metacontrast functions resemble one another. However, when visual angle, luminance, and duration vary from the values used in the Kahneman study, the resemblance between the two effects breaks down. Since the apparent motion explanation for metacontrast assumes an identity between apparent motion and metacontrast, these present results indicate that the apparent motion hypothesis for metacontrast is untenable. Metacontrast and apparent motion may not be unrelated, however; they might both have something to do with single units in the visualcortex. For each effect, however, different functional units would be involved.     

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.     

Metacontrast and brightness discrimination

An attempt was made to obtain U-shaped masking functions in two metacontrast experiments. Trained Ss judged whether a square test stimulus (TS) was bright or dim. The TS was presented alone or in conjunction with an adjacent pair of square masking stimuli (MS) whose energy equaled the bright TS. The stimulus onset asynchronies (SOA) rangedfrom 0 to 125 msec. The task minimized the role of apparent movement cues as a reliable basis for judgrnent. Similar studies have employed TS plus MS vs MS alone as the alternatives, allowing apparent movement to be a cue. Brightness accuracy was a U-shaped function of SOA. This finding is consistent with neural-net models (Weisstein, 1968). However, analysis of Ss’ response bias suggested an alternative explanation involving the MS as a comparison stimulus at short SOA. It was concluded that U-shaped masking functions are also consistent with theories based upon independent component processes, e.g., Schurman and Eriksen (1970) and Uttal (1970).     

Practice increases the efficiency of evidence accumulation in perceptual choice

Most models of choice response time base decisions on evidence accumulated over time. A fundamental distinction among these models concerns whether each piece of evidence is equally weighted (lossless accumulation) or unequally weighted (leaky accumulation). The authors tested a hypothesis derived from A. Heathcote and S. Brown's (2002) self-exciting expert competitor (SEEXC) model of skill acquisition: that evidence accumulation becomes less leaky with practice. The hypothesis was supported by observation that the effects of prime stimuli increased with practice. The authors used metacontrast masked primes, which could not be consciously discriminated by most participants, to avoid methodological problems associated with conscious strategy changes. The form of the law of practice in the data is also shown to be consistent with the SEEXC model.