Retinal masking during pursuit eye movements: implications for spatiotopic visual persistence

White (1976) reported that presentation of a masking stimulus during a pursuit eye movement interfered with the perception of a target stimulus that shared the same spatial, rather than retinal, coordinates as the mask. This finding has been interpreted as evidence for the existence of spatiotopic visual persistence. We doubted White's results because they implied a high degree of position constancy during pursuit eye movements, contrary to previous research, and because White did not monitor subjects' eye position during pursuit; if White's subjects did not make continuous pursuit eye movements, it might appear that masking was spatial when in fact it was retinal. We attempted to replicate White's results and found that when eye position was monitored to ensure that subjects made continuous pursuit movements, masking was retinal rather than spatial. Subjects' phenomenal impressions also indicated that retinal, rather than spatial, factors underlay performance in this task. The implications of these and other results regarding the existence of spatiotopic visual persistence are discussed.     

Gradual remapping results in early retinotopic and late spatiotopic inhibition of return

Here we report that immediately following the execution of an eye movement, oculomotor inhibition of return resides in retinotopic (eye-centered) coordinates. At longer postsaccadic intervals, inhibition resides in spatiotopic (world-centered) coordinates. These results are explained in terms of perisaccadic remapping. In the interval surrounding an eye movement, information is remapped within retinotopic maps to compensate for the retinal displacement. Because remapping is not an instantaneous process, a fast, but gradual, transfer of inhibition of return from retinotopic to spatiotopic coordinates can be observed in the postsaccadic interval. The observation that visual stability is preserved in inhibition of return is consistent with its function as a "foraging facilitator," which requires locations to be inhibited across multiple eye movements. The current results support the idea that the visual system is retinotopically organized and that the appearance of a spatiotopic organization is due to remapping of visual information to compensate for eye movements.     

The spatiotopic representation of visual objects across time

Each eye movement introduces changes in the retinal location of objects. How a stable spatiotopic representation emerges from such variable input is an important question for the study of vision. Researchers have classically probed human observers' performance in a task requiring a location judgment about an object presented at different locations across a saccade. Correct performance on this task requires realigning or remapping retinal locations to compensate for the saccade. A recent study showed that performance improved with longer presaccadic viewing time, suggesting that accurate spatiotopic representations take time to build up. The first goal of the study was to replicate that finding. Two experiments, one an exact replication and the second a modified version, failed to replicate improved performance with longer presaccadic viewing time. The second goal of this study was to examine the role of attention in constructing spatiotopic representations, as theoretical and neurophysiological accounts of remapping have proposed that only attended targets are remapped. A third experiment thus manipulated attention with a spatial cueing paradigm and compared transsaccadic location performance of attended versus unattended targets. No difference in spatiotopic performance was found between attended and unattended targets. Although only negative results are reported, they might nevertheless suggest that spatiotopic representations are relatively stable over time.     

Two forms of persistence in visual information processing

Iconic memory, which was initially regarded as a unitary phenomenon, has since been subdivided into several components. In the present work we examined the joint effects of two such components (visible persistence and the visual analog representation) on performance in a partial report task. The display consisted of 15 alphabetic characters arranged around the perimeter of an imaginary circle on the face of an oscilloscope. The observer named the character singled out by a bar-probe. Two factors were varied: exposure duration of the array (10, 50, 100, 150, 200, 300, 400 or 500 ms) and duration of blank period (interstimulus interval, ISI) between the termination of the array and the onset of the probe (0, 50, 100, 150, or 200 ms). Performance was progressively impaired as both exposure duration and ISI were increased. The results were explained in terms of a probabilistic combinatorial model in which the timecourses of visible persistence and of the visual analog representation are regarded as time-locked to the onset and to the end of stimulation, respectively. The impairing effect of exposure duration was attributed to the relatively high spatial demands of the task that could be met optimally by information in visible persistence (which declines as a function of exposure duration), but less adequately by information in the visual analog representation. A second experiment, employing a task with lesser spatial demands, confirmed this interpretation.     

The role of visible persistence for perception of visual bilateral symmetry1

Abstract: Although the detection of visual bilateral symmetry has been claimed to be highly efficient, the possible involvement and function of visual memory in such efficient mechanisms has rarely been examined. We hypothesized that symmetry perception is rapid, as it can be achieved from rapidly decaying information of visible persistence. To test this hypothesis, we employed a temporal integration paradigm. A symmetric dot pattern was randomly divided into two asymmetric patterns and presented successively with a blank screen presented between patterns. Observers could detect symmetry when the two patterns were presented close in time (Experiment 1), indicating that observers perceived symmetry presumably utilizing visible persistence. In addition, the inverse‐intensity effect of visible persistence (Di Lollo & Bischof, 1995) was evident in our temporal integration task of symmetry (Experiment 2). The results of the current study clearly demonstrate that the detection of symmetry can be achieved based on the visible persistence. The large capacity and high spatial precision of visible persistence might be adequate for the rapid and spatially global encoding of visual symmetry.     

The changing face of visual persistence

In three experiments, the effect of target luminance on estimates of visual persistence was determined on a popular successive-field task. Even though the experiments differed from each other only in terms of minor changes in stimulus conditions, very different effects were obtained across the three experiments. The different findings were attributed to the often overlooked roles of masking and target degradation on tasks of persistence. Implications for the numerous contradictory findings in the persistence literature are discussed, and the current popularity of the successive-field task is questioned.     

The extraction of information from visual persistence.

Seven-letter targets were flashed for 50 msec and followed by either a blank adapting field (persisting representation of the stimulus fully available) or a series of continuous cycles of target and mask until the cumulative duration of the target matched the estimated duration of visual persistence (stimulus physically present for same interval as representation). The reportability of information from the targets in the latter case was only 50% that in the former. The interpretation is that visual persistence is an active, continuously operating process rather than a passive neural copy of the stimulus.     

The effect of spatial frequency and contrast on visual persistence

The visual persistence of sinusoidal gratings of varying spatial frequency and contrast was measured. It was found that the persistence of low-contrast gratings was longer than that of high-contrast stimuli for all spatial frequencies investigated. At higher contrast levels of 1 and 4 cycles deg-1 gratings, a tendency for persistence to be independent of contrast was observed. For 12 cycles deg-1 gratings, however, persistence continued to decrease with increasing contrast. These results are compared with recently published data on other temporal responses, and are discussed in terms of the different properties of sustained and transient channels.     

Generality of persistence: The role of stimulus and response factors in persistence to punishment

Previous research has shown that intermittent punishment of a response increases its persistence to continuous punishment and that intermittent punishment training in one situation produces persistence to continuous punishment in other situations. Experiment 1 showed that as long as the instrumental response and punishing stimulus were held constant from intermittent to continuous punishment marked differences between these situations had no decremental effect on persistence. Experiment 2 showed that intermittent punishment training of one response resulted in substantial persistence to continuous punishment of a different and apparently incompatible response and that such response change had no more than a marginal effect on persistence. The results were seen as requiring some revision to the traditional conditioning-model interpretation of persistence to punishment.     

Cortical dynamics of visual persistence and temporal integration

In a temporal integration experiment, subjects must integrate two visual stimuli, presented at separate times, to perform an identification task. Many researchers have assumed that the persistence of the leading stimulus determines the ability to integrate the leading and trailing stimuli. However, recent studies of temporal integration have challenged that hypothesis by demonstrating that several theories of persistence are incompatible with data on temporal integration. This paper shows that an account of visual persistence given by a neural network model of preattentive vision, called the boundary contour system, explains data on temporal integration. Computer simulations of the model explain why temporal integration becomes more difficult when the display elements are separated by longer interstimulus intervals or are of longer duration or of higher luminance, or are spatially closer together. The model suggests that different mechanisms underlie the inverse duration effects for leading and for trailing elements. The model further predicts interactions of spatial separation, duration, and luminance of the trailing display.     

The relationship between visual persistence and event perception in bistable motion display

Observers viewed two alternating frames, each consisting of three rectangular bars displaced laterally by one cycle in one frame with respect to the other. At long interframe intervals (IFIs) observers perceived a group of three bars moving as a whole (group motion), and at short IFIs the overlapping elements in the two frames appeared stationary, while the third element appeared to move from one end of the display to the other (element motion). The upper temporal limit for perceiving element motion was reduced when bars with blurred edges were used and when either frame duration or bar size was increased. However, when inner and outer elements had different sizes, the element motion percept was dominant up to 230 ms IFI. These findings may be interpreted in terms of spatial tuning of motion mechanisms involved in the perception of bistable apparent motion.     

The contribution of visual persistence to the perceived duration of brief targets

Two experiments were conducted to examine the role of sensory persistence on tasks of perceived duration employing very brief visual stimuli. Using a standard temporal judgment task, the first experiment replicated both the “size effect” and “empty-filled” illusion reported by previous investigators. However, entirely comparable results were also found with a probematching task, which theoretically assesses the degree of persistence exhibited by a stimulus. The second experiment examined the effect of target luminance on perceived duration. Consistent with a sensory persistence interpretation, judgments of duration increased with increasing luminance. The results from the two experiments were discussed in terms of varying degrees of retinal persistence produced by different stimuli. This view was contrasted with currently dominant interpretations that postulate changes in perceived duration to reflect different information-processing requirements across stimulus conditions.