Dynamic visual noise reduces confidence in short-term memory for visual information

Previous research has shown effects of the visual interference technique, dynamic visual noise (DVN), on visual imagery, but not on visual short-term memory, unless retention of precise visual detail is required. This study tested the prediction that DVN does also affect retention of gross visual information, specifically by reducing confidence. Participants performed a matrix pattern memory task with three retention interval interference conditions (DVN, static visual noise and no interference control) that varied from trial to trial. At recall, participants indicated whether or not they were sure of their responses. As in previous research, DVN did not impair recall accuracy or latency on the task, but it did reduce recall confidence relative to static visual noise and no interference. We conclude that DVN does distort visual representations in short-term memory, but standard coarse-grained recall measures are insensitive to these distortions.     

Short-term visual memory for location in depth: A U-shaped function of time

Short-term visual memory was studied by displaying arrays of four or five numerals, each numeral in its own depth plane, followed after various delays by an arrow cue shown in one of the depth planes. Subjects reported the numeral at the depth cued by the arrow. Accuracy fell with increasing cue delay for the first 500 ms or so, and then recovered almost fully. This dipping pattern contrasts with the usual iconic decay observed for memory traces. The dip occurred with or without a verbal or color–shape retention load on working memory. In contrast, accuracy did not change with delay when a tonal cue replaced the arrow cue. We hypothesized that information concerning the depths of the numerals decays over time in sensory memory, but that cued recall is aided later on by transfer to a visual memory specialized for depth. This transfer is sufficiently rapid with a tonal cue to compensate for the sensory decay, but it is slowed by the need to tag the arrow cue’s depth relative to the depths of the numerals, exposing a dip when sensation has decayed and transfer is not yet complete. A model with a fixed rate of sensory decay and varied transfer rates across individuals captures the dip as well as the cue modality effect.     

The medial temporal lobe and visual working memory: Comparisons across tasks, delays, and visual similarity

Whether the hippocampus and medial temporal lobe (MTL) play any important role in visual working memory is a relatively new and controversial research question. The primary goal of this study was to assess working memory for faces over very short delays in patients with MTL damage. Patients and matched controls were required to remember one face that was parametrically morphed to be more or less similar to a probe face, over either a 1- or an 8-sec delay. Memory was assessed using both forced choice and old-new recognition tasks. The results show that MTL damage impairs both speed and accuracy of visual working memory across tasks. We speculate that the hippocampus is generally necessary for memory encoding.     

Perceptual economy and the impression of visual depth

Three experiments were carried out to investigate the hypothesis that the impression of visual depth given by gradient patterns is due to the operation of a principle of “perceptual economy.” The first experiment showed that the greater the number of values of the gradient variables in a pattern, the stronger was the tridimensional impression given by that pattern. The second showed that the greater the number of gradient variables, the less the amount of the pattern that had to be exposed before a tridimensional response was elicited. The third showed that judged slants increased as a function of the number of gradient variables in each pattern. The results suggest that the impression of visual depth given by a pattern represents a compromise between the economy gained from making a tridimensional specification of the elements in the pattern and the possible cost of making an error in coding the information in this way.     

Static visual noise and the ansbacher effect

In Experiment I subjects made estimates of the apparent length of a 12 cm. long light arc-line rotating around a central fixation point at arc speeds of 66, 99, 132 and 165 cm./sec. Apparent contraction of the arc occurred as a function of speed, there being greater contraction in the presence of a superimposed random pattern of I cm. light squares (visual noise) than in its absence. The results of Experiment II indicated that there was no significant difference in length due to visual noise when the arcs were stationary. In Experiment III subjects made estimates of the speed of rotation of the arc and it was found that visual noise did not significantly affect the apparent arc-speed.     

Modelling visual detection: Luminance response non-linearity and internal noise

Two experiments that investigate the effect of various display factors on the detectability of a thin line signal in random visual noise are described. Three statistical decision models are described, together with their ability to account for the results. The first is an “ideal detector” model, the second an “energy integrator” model, and the third a model based upon the operation of retinal ganglion cells which incorporates a gain control mechanism. The ideal detector model fails to give a good account of human performance, whereas the other two models provide a good fit to the data. The digital Laplacian with gain control model has the slight advantage over the energy integrating model in being able to account for a small superiority in the detection of dark as opposed to bright signals. Finally, both models require the inclusion of an estimate of the internal noise of the human visual system to account for the pattern of performance observed under changing conditions of display contrast.     

Visual prediction: psychophysics and neurophysiology of compensation for time delays

A necessary consequence of the nature of neural transmission systems is that as change in the physical state of a time-varying event takes place, delays produce error between the instantaneous registered state and the external state. Another source of delay is the transmission of internal motor commands to muscles and the inertia of the musculoskeletal system. How does the central nervous system compensate for these pervasive delays? Although it has been argued that delay compensation occurs late in the motor planning stages, even the earliest visual processes, such as phototransduction, contribute significantly to delays. I argue that compensation is not an exclusive property of the motor system, but rather, is a pervasive feature of the central nervous system (CNS) organization. Although the motor planning system may contain a highly flexible compensation mechanism, accounting not just for delays but also variability in delays (e.g., those resulting from variations in luminance contrast, internal body temperature, muscle fatigue, etc.), visual mechanisms also contribute to compensation. Previous suggestions of this notion of "visual prediction" led to a lively debate producing re-examination of previous arguments, new analyses, and review of the experiments presented here. Understanding visual prediction will inform our theories of sensory processes and visual perception, and will impact our notion of visual awareness.     

Strategies for visual word recognition and orthographical depth: a multilingual comparison

We investigated the psychological reality of the concept of orthographical depth and its influence on visual word recognition by examining naming performance in Hebrew, English, and Serbo-Croatian. We ran three sets of experiments in which we used native speakers and identical experimental methods in each language. Experiment 1 revealed that the lexical status of the stimulus (high-frequency words, low-frequency words, and nonwords) significantly affected naming in Hebrew (the deepest of the three orthographies). This effect was only moderate in English and nonsignificant in Serbo-Croatian (the shallowest of the three orthographies). Moreover, only in Hebrew did lexical status have similar effects on naming and lexical decision performance. Experiment 2 revealed that semantic priming effects in naming were larger in Hebrew than in English and completely absent in Serbo-Croatian. Experiment 3 revealed that a large proportion of nonlexical tokens (nonwords) in the stimulus list affects naming words in Hebrew and in English, but not in Serbo-Croatian. These results were interpreted as strong support for the orthographical depth hypothesis and suggest, in general, that in shallow orthographies phonology is generated directly from print, whereas in deep orthographies phonology is derived from the internal lexicon.     

Visual processing of coherent rotation in the central visual field: an fMRI study

Functional magnetic resonance imaging was used to determine the brain areas that process coherent motion. To reduce the activity related to eye-movement planning and self-motion perception, rotation was used as coherent motion and the stimulus was restricted to the central visual field. Coherent rotation relative to incoherent random-dot motion resulted in consistent activation in the superior parietal lobule (SPL), in the lateral occipital gyrus (presumptive kinetic occipital region, KO), and in the fusiform gyrus (FG). The main novel finding in present study is the bilateral SPL activation, which has not been found in any previous study contrasting coherent and incoherent motion. It is suggested that the SPL activation is related to form-from-motion processing. The stimulus modification that prevented abrupt appearances of dots at the borders of the stimulus field increased the strength of rolling disk-like percept of the coherent stimulus. This perception of form may also be at least partly responsible for the activation in KO and FG. With this explanation, our three consistent activation areas are in line with previous findings. Furthermore, these results demonstrate that even delicate changes in some stimulus aspects can lead to significant changes in the activation of the brain.     

Infants' coordination of auditory and visual depth information.

Using the preferential-looking procedure infants 5, 7, and 9 months of age were presented two videoimages side by side on separate monitors accompanied by a soundtrack that matched one of the images. Each infant was presented: (1) a stationary drum-beating toy paired with the same toy approaching and receding in depth, to assess infants' recognition both that changing sound amplitude is a property of an object that is moving in space and that constancy in amplitude is a property of a stationary object; (2) a drum-beating toy moving horizontally paired with one approaching and receding in depth, to assess infants' recognition that systematic increases and decreases in amplitude accompany object movement in a particular dimension, namely depth; and (3) two identical toys alternately approaching and receding in depth but out of phase (i.e., one approaching while the other is receding), to assess infants' recognition that increases and decreases in amplitude accompany a particular type of object movement in depth. Measures of mean duration of looking time indicated that the 5-month-olds looked reliably to the correct videoimage only for the stationary toy paired with the constant amplitude sound. The 7-month-olds recognized that changes in amplitude accompany object movement in depth but did not coordinate auditory with visual depth information as well as older infants. The 9-month-olds looked reliably to the correct videoimages in all conditions. Possible contributing factors to these developmental trends in performance are discussed.     

Reaction time and visual brightness: within-subject correlations.

An experiment was conducted to compare visual reaction time and visual brightness within the same subjects. Simple reaction times and magnitude estimates of brightness were obtained in response to 1000-msec. flashes of 60.7, 67.5, 76.4, 85.1, and 93.4 dB re 10(-10)L white light. The relationship between reaction time and stimulus intensity was best described by a negative logarithmic function, while the relationship between magnitude estimates of brightness and stimulus intensity was best described by a power function. Linear correlations between reaction times and magnitude estimates indicated that visual reaction time and brightness are not proportional within all subjects. Previous reports of proportionality between these two measures were discussed as possibly being the result of inappropriate cross-experiment comparisons.     

Motion parallax driven by head movements: conditions for visual stability, perceived depth, and perceived concomitant motion

Yoking the movement of the stimulus on the screen to the movement of the head, we examined visual stability and depth perception as a function of head-movement velocity and parallax. In experiment 1, for different head velocities, observers adjusted the parallax to find (a) the depth threshold and (b) the concomitant-motion threshold. Between these thresholds, depth was seen with no perceived motion. In experiment 2, for different head velocities, observers adjusted the parallax to produce the same perceived depth. A slower head movement required a greater parallax to produce the same perceived depth as faster head movements. In experiment 3, observers reported the perceived depth for different parallax magnitudes. Perceived depth covaried with smaller parallax without motion perception, but began to decrease with larger parallax and concomitant motion was seen. Only motion was seen with the larger parallax.     

Dynamic occlusion and motion parallax in depth perception

Random-dot techniques were used to examine the interactions between the depth cues of dynamic occlusion and motion parallax in the perception of three-dimensional (3-D) structures, in two different situations: (a) when an observer moved laterally with respect to a rigid 3-D structure, and (b) when surfaces at different distances moved with respect to a stationary observer. In condition (a), the extent of accretion/deletion (dynamic occlusion) and the amount of relative motion (motion parallax) were both linked to the motion of the observer. When the two cues specified opposite, and therefore contradictory, depth orders, the perceived order in depth of the simulated surfaces was dependent on the magnitude of the depth separation. For small depth separations, motion parallax determined the perceived order, whereas for large separations it was determined by dynamic occlusion. In condition (b), where the motion parallax cues for depth order were inherently ambiguous, depth order was determined principally by the unambiguous occlusion information.     

The time course of visual afterimages: data and theory

Sequential viewing of two orthogonally related patterns produces an afterimage of the first pattern (Vidyasagar et al, 1999 Nature 399 422-423; Francis and Rothmayer, 2003 Perception and Psychophysics 65 508-522). We investigated how the timing between the first stimulus (a vertical bar grating) and the second stimulus (a horizontal bar grating) affected the visibility of the afterimage (a perceived vertical grating). As the duration from offset of the first stimulus increased, reports of afterimages decreased. Holding fixed the total time from offset of the first stimulus and increasing the duration from offset of the second stimulus while decreasing the time between the first and second stimuli, caused a decrease in afterimage reports. We interpret this finding in terms of Grossberg's BCS - FCS (boundary contour system--feature contour system) theory. In this theory, the afterimage percept is the result of color complement after-responses in the FCS system interacting with orientation after-responses in the BCS system. The two types of after-responses interact at a stage of neural filling-in to produce the afterimage percept. As the duration between the stimuli increases, the color after-responses weaken so that visible filling-in is less likely to occur. A similar effect occurs for the orientation after-responses but at a faster time scale. Simulations of the model match the experimental data.     

Segregation by color and stereoscopic depth in three-dimensional visual space

Two experiments were conducted to investigate how color and stereoscopic depth information are used to segregate objects for visual search in three-dimensional (3-D) visual space. Eight observers were asked to indicate the alphanumeric category (letter or digit) of the target which had its unique color and unique depth plane. In Experiment 1, distractors sharing a common depth plane or a common color appeared in spatial contiguity in thexy plane. The results suggest that visual search for the target involves examination of kernels formed by homogeneous items sharing the same color and depth. In Experiment 2, thexy contiguity of distractors sharing a common color or a common depth plane was varied. The results showed that when target-distractor distinction becomes more difficult on one dimension, the other dimension becomes more important in performing visual search, as indicated by a larger effect on search time. This suggests that observers can make optimal use of the information available. Finally, color had a larger effect on search time than did stereoscopic depth. Overall, the results support models of visual processing which maintain that perceptual segregation and selective attention are determined by similarity among objects in 3-D visual space on both spatial and nonspatial stimulus dimensions.     

Noise and visual choice-reaction time: A large-scale population survey

The impact of a 80 dB(A) intermittent broadband noise on a three-choice visual reaction time (RT) task was investigated. There were 2661 subjects who represented the healthy Finnish population from the age of 30 to 79 years. Noise slowed down the response speed highly significantly but the main effect was negligible in the psychological sense (513 vs. 506 msec). The performance of the elderly was more affected than that of the young. Slow responders did not show any detrimental effect of noise irrespective of whether or not they committed errors. The results are discussed in terms of person-induced ways to perform and cope under a mild stress.     

On the rate of acquisition of visual information about space,time, and intensity

The temporal course of acquisition of visual information was mapped by measuring the speed and accuracy With which Ss could discriminate the position, intensity, or duration of a stimulus that was varied independently on these three binary dimensions. The speed-accuracy tradeoff was different for each of the three discrimination tasks, with performance substantially superior in the position discrimination task. In the intensity and duration discrimination tasks, there were systematic changes with RT in the relative influences of the three stimulus variables over the two alternative responses, suggesting .three phases of the corresponding perceptual processes: an initial dominance by position of the stimulus, a subsequent, joint influence by both intensity and duration, and finally an exclusive control by the correct dimension. The results demonstrate that Ss can selectively attend to various dimensions of the same stimulus, with concommitantly varying time constants. The perceptual processes being tapped by a discrimination task depend upon instructions and upon RT.