Visual information processing in relation to age and to reading ability.

Temporal aspects of early visual information processing were studied developmentally in good and in poor reading male subjects ranging in age from 7 to 13 years. Forced-choice temporal integration and backward masking tasks, respectively, were utilized to assess duration of visual persistence and of relative rate of visual information processing. The results did not reveal differences in either visual persistence or processing rate in relation to reading ability at any age level studied. However, processing rate was found to increase markedly with chronological age in both the good and the poor readers while visual persistence did not vary significantly. The findings were discussed in relation to earlier work and in relation to current theoretical formulations of visual information processing.     

The speed of visual processing in children and adults: Effects of backward and forward masking

Children, 4-5 and 9-10 years old, and college-age adults were tested on two visual masking tasks. The first task required the Ss to identify whether a tachistoscopically presented bar was horizontal or vertical The second task, also using tachistoscopic presentation of stimuli, required Ss to locate a horizontal (or vertical) bar in a matrix of vertical (or horizontal) bars. In both tasks, backward masking produced greater disruption than did forward masking, and the amount of disruption induced by both backward and forward masking decreased as age increased. An Age by Masking Condition interaction was found only in the location task and reflected a much greater difference between backward- and forward-masking conditions for the youngest group than for the older groups. On the basis of these findings and other considerations, it was concluded that only in the location task, which presumably required visual search, was the speed of visual processing slower in the younger group.     

Does backward masking by visual noise stop stimulus processing?

The identification of one, two, and four random letters was studied under three procedures: (1) backward masking by a visual noise; (2) concurrent masking by a visual noise; and (3) no masking. With backward masking the number of letters correctly identified was independent of the number presented. Direct judgments of the duration, brightness, contrast, sharpness, and texture of the letters were also made. Under backward masking the letters appeared to be on for a very brief duration, but with high apparent contrast. The results indicate that backward masking impairs identification by interrupting the stimulus processing, not by degrading the stimulus input.     

Age effects in backward visual masking (Crawford paradigm)

Fifteen Ss in each of four age groups (5-, 10-, 16-, and 22–23-years old) received backward visual masking. Group effects occurred at longer ISIs indicating slower prerecognition processing for younger Ss. In a second experiment 19-, 35-, and 55-year-old Ss were administered backward visual masking under the identical procedures of Exp. 1. The oldest Ss performed significantly worse than 19- and 35-year-old Ss, which did not differ significantly from each other. The general methodological features of both studies, as well as the obtained relationships were discussed.     

Attentional mechanisms in visual signal detection: the effects of simultaneous and delayed noise and pattern masks

The attentional cuing effects in detection and some discrimination tasks depend on the use of backward masks and on the presence of external noise in the display. These effects have been attributed to an interruption masking mechanism, which terminates stimulus processing prematurely, and an external noise exclusion mechanism, which minimizes the perceptual effects of noise. To test whether the dependencies on masking and external noise are expressions of a single mechanism, observers detected grating patch stimuli, masked with noise masks or pattern masks, presented either simultaneously or after a delay of 60-90 msec. Contrary to an external noise exclusion account, but consistent with an interruption masking account, cuing effects were largest when the masks were delayed. However, weaker cuing effects were obtained with simultaneous masks, contrary to an interruption masking account. These results suggest that attentional effects in simple visual judgments are affected by mechanisms of both kinds.     

Iconic memory and visible persistence

There are three senses in which a visual stimulus may be said to persist psychologically for some time after its physical offset. First, neural activity in the visual system evoked by the stimulus may continue after stimulus offset (“neural persistence”). Second, the stimulus may continue to be visible for some time after its offset (“visible persistence”). Finally, information about visual properties of the stimulus may continue to be available to an observer for some time after stimulus offset (“informational persistence”). These three forms of visual persistence are widely assumed to reflect a single underlying process: a decaying visual trace that (1) consists of afteractivity in the visual system, (2) is visible, and (3) is the source of visual information in experiments on decaying visual memory. It is argued here that this assumption is incorrect. Studies of visible persistence are reviewed; seven different techniques that have been used for investigating visible persistence are identified, and it is pointed out that numerous studies using a variety of techniques have demonstrated two fundamental properties of visible persistence: theinverse duration effect (the longer a stimulus lasts, the shorter is its persistence after stimulus offset) and theinverse intensity effect (the more intense the stimulus, the briefer its persistence). Only when stimuli are so intense as to produce afterimages do these two effects fail to occur. Work on neural persistences is briefly reviewed; such persistences exist at the photoreceptor level and at various stages in the visual pathways. It is proposed that visible persistence depends upon both of these types of neural persistence; furthermore, there must be an additional neural locus, since a purely stereoscopic (and hence cortical) form of visible persistence exists. It is argued that informational persistence is defined by the use of the partial report methods introduced by Averbach and Coriell (1961) and Sperling (1960), and the term “iconic memory” is used to describe this form of persistence. Several studies of the effects of stimulus duration and stimulus intensity upon the duration of iconic memory have been carried out. Their results demonstrate that the duration of iconic memory is not inversely related to stimulus duration or stimulus intensity. It follows that informational persistence or iconic memory cannot be identified with visible persistence, since they have fundamentally different properties. One implication of this claim that one cannot investigate iconic memory by tasks that require the subject to make phenomenological judgments about the duration of a visual display. In other words, the so-called “direct methods” for studying iconic memory do not provide information about iconic memory. Another implication is that iconic memory is not intimately tied to processes going on in the visual system (as visible persistence is); provided a stimulus is adequately legible, its physical parameters have little influence upon its iconic memory. The paper concludes by pointing out that there exists an alternative to the usual view of iconic memory as a precategorical sensory buffer. According to this alternative, iconic memory is post-categorical, occurring subsequent to stimulus identification. Here, stimulus identification is considered to be a rapid automatic process which does not require buffer storage, but which provides no information about episodic properties of a visual stimulus. Information about these physical stimulus properties must, in some way, be temporarily attached to a representation of the stimulus in semantic memory; and it is this temporarily attached physical information which constitutes iconic memory.     

Further evidence for two components in visual persistence.

The phenomenal durations of tachistoscopically presented letter arrays at five levels of redundancy were measured using a subtractive reaction-time technique. Phenomenal duration was inversely related to redundancy only when report of the letters was required. The duration of functional availability of stimulus information for stimuli at the five levels of redundancy was determined in a backward masking paradigm. The measurements of the duration of functional availability and phenomenal presence were convergent, indicating that one process is responsible for both the phenomenal and functional duration of a persisting representation of a visual stimulus. The results are interpreted as providing further evidence for two components in visual persistence: a physical component whose duration is unrelated to stimulus parameters and an informational component whose duration is inversely related to the efficiency of encoding stimulus information.     

What's new in visual masking?

A brief display that is clearly visible when shown alone can be rendered invisible by the subsequent presentation of a second visual stimulus. Several recently described backward masking effects are not predicted by current theories of visual masking, including masking by four small dots that surround (but do not touch) a target object and masking by a surrounding object that remains on display after the target object has been turned off. A crucial factor in both of these effects is attention: almost no masking occurs if attention can be rapidly focused on the target, whereas powerful masking ensues if attention directed at the target is delayed. A new theory of visual masking, inspired by developments in neuroscience, can account for these effects, as well as more traditional masking effects. In addition, the new theory sheds light on related research, such as the attentional blink, inattentional blindness and change blindness.     

Duration of visible persistence in relation to range of spatial frequencies

Five experiments examined the relationship between range of spatial frequencies contained in a visual display and duration of visible persistence. The high spatial frequency contents of the display were reduced by defocusing the image at the retina. Duration of visible persistence was measured by a task that required perceptual integration of a pattern whose parts were displayed sequentially in time. Experiments 1 and 2 showed that progressive reductions in the high-frequency contents of the display produced corresponding decrements in the duration of visible persistence. Experiments 3, 4, 5 showed that decrements in the duration of visible persistence could not be attributed to changes in the apparent size or in the brightness of the display brought about by defocusing. The results were interpreted in terms of the temporal response properties of perceptual mechanisms attuned to separate ranges of spatial frequencies. Strong parallels were drawn with the multichannel theory of visual information processing proposed by Breitmeyer and Ganz.     

Recent models and findings in visual backward masking: a comparison, review, and update

Visual backward masking not only is an empirically rich and theoretically interesting phenomenon but also has found increasing application as a powerful methodological tool in studies of visual information processing and as a useful instrument for investigating visual function in a variety of specific subject populations. Since the dual-channel, sustained-transient approach to visual masking was introduced about two decades ago, several new models of backward masking and metacontrast have been proposed as alternative approaches to visual masking. In this article, we outline, review, and evaluate three such approaches: an extension of the dual-channel approach as realized in the neural network model of retino-cortical dynamics (Ogmen, 1993), the perceptual retouch theory (Bachmann, 1984, 1994), and the boundary contour system (Francis, 1997; Grossberg & Mingolla, 1985b). Recent psychophysical and electrophysiological findings relevant to backward masking are reviewed and, whenever possible, are related to the aforementioned models. Besides noting the positive aspects of these models, we also list their problems and suggest changes that may improve them and experiments that can empirically test them.     

A cross-sequential analysis of developmental differences in speed of visual information processing

Development of processing speed was examined in three backward masking studies. The first verified the central nature of backward masking for children aged 8 and 11 years and for adults. The second suggested that task requirements were equivalent for children similar to those in Study 1, and that age differences in performance were not attributable to nonprocessing variables. The main cross-sequential study estimated speed of processing in 80 children (approximately 6 years to 13 years) and young adults using an inspection time task. Target exposure duration was varied to establish the time required to achieve a high level of discriminative accuracy. Estimates of processing speed increased until about 11-13 years of age; beyond this, the trend was less obvious, and it is possible that inspection time asymptotes at around the onset of adolescence. Performance improvement after 1 year could not be explained as resulting from practice since improvement among controls over a period of 2 weeks was significantly less. Correlations between estimates of inspection time made up to 2 years apart found the measure to be reliable.     

Temporal processing and psychosis proneness

Two measures of temporal processing: critical stimulus duration (CSD) and visual backward masking (VBM), were examined in a group of normal subjects whose predisposition to psychosis was assessed using the psychoticism (P) scale from Eysenck's Personality Questionnaire. The current study employed the method of constant stimuli with a two-alternative forced choice responding to reduce the variability in CSD-data. Higher P scorers required a significant longer target stimulus duration in order to correctly identify the stimulus than lower P scorers. These results suggest that subjects prone to psychosis possess a relatively less sensitive temporal processing system than low P scorers. Performance in the subsequent masking phase revealed no evidence of a VBM deficit. It was not possible to explain this pattern of results in terms of task difficulty. The findings were discussed in terms of potential inadequacies in previous calculations of CSD. This possibility requires further testing before the backward masking deficit can be adopted as a trait marker for schizophrenia.     

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 recogition of dot-pattern bigrams: an extension and replication.

The study examined visual recognition of bigrams, each formed from a pair of "random" dot patterns, as a function of stimulus offset asynchrony and duration. The results replicate and extend those of an earlier study by showing that the effect of backward masking in vision, where the mask is actually a part of the preceding composite target, is limited to about 250 to 300 msec. This time interval is suggested as that required to complete the processing of that composite target. The results may be understood in terms of an interruption hypothesis, with selective attention and/or discontinuity detectors as mechanisms possibly involved in the masking process.     

A Comparison of Two Lateral Inhibitory Models of Metacontrast

Metacontrast, an apparent reduction in brightness of a target that is followed by a non-overlapping mask, has been modeled with simulated neural nets incorporating either recurrent lateral inhibition or forward and backward inhibition with lateral components. A one-layer lateral inhibitory model (B. Bridgeman, 1971, Psychological Review 78, 528-539) and a six-layer model (G. Francis, 1997, Psychological Review 104, 572-594) both simulate the basic metacontrast effect, showing that stimulus-dependent activity that reverberates for some time in the model after stimulus offset is essential to simulate metacontrast. The six-layer model does not simulate monotonic masking with low response criterion, an essential property of metacontrast; the lateral inhibitory model uses duration of reverberation to simulate the criterion. Each model simulates several variations of masking, such as changing the relative energy of target and mask, but neither can handle effects of practice or attention that apparently engage higher processing levels. Copyright 2001 Academic Press.     

Information persistence in the integration of partial cues for object recognition

A great many studies have shown that the perceptual effects of very brief visual stimuli can persist beyond the duration of the stimulus itself. These effects include sustained perception of the stimulus even though it is no longer present and the integration of information across an interstimulus interval. These two forms of sustained activity can be characterized as visible persistence and information persistence. Iconic memory protocols and a number of discrimination tasks have demonstrated the existence of information persistence that can last up to several hundred milliseconds, but there is little evidence that the cues needed for identification of objects can be transferred across intervals in this range. In the present experiments, a minimal transient discrete cue protocol was used to demonstrate that shape cues, these being provided by subsets of dots that mark the outer boundary of nameable objects, can be integrated over several hundred milliseconds and that the duration is a function of ambient room illumination. The experiments further evaluated whether this information persistence is mediated by visible persistence. Although both perceptual effects have durations that are an inverse function of room illumination, the ability to integrate partial shape cues was not determined by the duration of visible persistence.     

Modeling spatial and temporal aspects of visual backward masking

Visual backward masking is a versatile tool for understanding principles and limitations of visual information processing in the human brain. However, the mechanisms underlying masking are still poorly understood. In the current contribution, the authors show that a structurally simple mathematical model can explain many spatial and temporal effects in visual masking, such as spatial layout effects on pattern masking and B-type masking. Specifically, the authors show that lateral excitation and inhibition on different length scales, in combination with the typical time scales, are capable of producing a rich, dynamic behavior that explains this multitude of masking phenomena in a single, biophysically motivated model.     

Two-stage model of visual backward masking: Sensory transmission and accrual of effective information as a function of target intensity and similarity

A functional model is used to describe the effect of target intensity and target-set similarity on backward visual masking. The model consists of two distinct stages of visual information processing. The first stage is related to sensory transduction and transmission and is assumed to require a finite and measurable amount of time during which performance-remains at chance. The second stage, associated with central processing, is characterized by a negatively accelerated growth function reflecting the accrual of effective information. Results show that the duration of the transmission stage is inversely related to target intensity. Surprisingly, the rate of information accrual is an interactive function of both target intensity and target-set similarity. The pattern of results is consistent with the interpretation that both intensity and similarity mediate their effect through a common mechanism—the accrual of effective information.     

Two-stage model of visual backward masking: sensory transmission and accrual of effective information as a function of target intensity and similarity.

A functional model is used to describe the effect of target intensity and target-set similarity on backward visual masking. The model consists of two distinct stages of visual information processing. The first stage is related to sensory transduction and transmission and is assumed to require a finite and measurable amount of time during which performance remains at chance. The second stage, associated with central processing, is characterized by a negatively accelerated growth function reflecting the accrual of effective information. Results show that the duration of the transmission stage is inversely related to target intensity. Surprisingly, the rate of information accrual is an interactive function of both target intensity and target-set similarity. The pattern of results is consistent with the interpretation that both intensity and similarity mediate their effect through a common mechanism--the accrual of effective information.