Visual motion interferes with tactile motion perception

Previous studies have demonstrated that visual apparent motion can alter the judgment of auditory apparent motion. We investigated the effect of visual apparent motion on judgments of the direction of tactile apparent motion. When visual motion was presented at the same time as, but in a direction opposite to, tactile motion, accuracy in judging the direction of tactile apparent motion was substantially reduced. This reduction in performance is referred to as 'the congruency effect'. Similar effects were observed when the visual display was placed either near to the tactile display or at some distance from the tactile display (experiment 1). In experiment 2, the relative alignment between the visual and tactile directions of motion was varied. The size of the congruency effect was similar at 0 degrees and 45 degrees alignments but much reduced at a 90 degrees alignment. In experiment 3, subjects made confidence ratings of their judgments of the direction of the tactile motion. The results indicated that the congruency effect was not due to subjects being unsure of the direction of motion and being forced to guess. In experiment 4, static visual stimuli were shown to have no effect on the judgments of direction of the tactile stimuli. The extent to which the congruency effect reflects capture effects and is the result of perceptual versus post-perceptual processes is discussed.     

Changes in motion perception following oculomotor smooth pursuit adaptation

The hypothesis that oculomotor smooth pursuit (SP) adaptation is accompanied by alterations in velocity perception was tested by assessing coherence thresholds, using random-dot kinematograms before and after the adaptation paradigm. The results showed that the sensitivity to coherent motion at 10 deg/sec (the initial target velocity during adaptation) was reduced after the SP adaptation, ending up at a level that was between those normally observed for velocities of 10 and 20 deg/sec. This is consistent with an overestimation of the velocity of the coherent motion and suggests that SP adaptation alters not only the oculomotor output, but also the perception of target velocity.     

Adaptation in motion perception: Alteration of motion evoked by ocular pursuit

A new perceptual adaptation, an alteration in the perceived direction of motion given by ocular pursuit, is reported. When an object starts to move on a straight path, its displacement is initially given by a shift of its image on the retinas of the stationary eyes; then, after about 200 msec, the eyes start to track the moving object. The perception of motion that results from ocular pursuit was altered by causing ocular pursuit of a moving object to be preceded regularly by a displacement of the object’s image whose direction differed from the direction of the pursuit movement. This was arranged by changing the direction of the given motion at approximately the moment when image displacement changed into tracking. Prolonged exposure to such conditions resulted in a change of the tracked motion’s apparent direction, which became somewhat more like the direction of the preceding motion phase that was given by image displacement.     

Spatio-temporal differentiation and integration in visual motion perception

Summary Perceptual organization during short tachistoscopic presentation of stimulus patterns formed by ten moving bright spots, representing a human body in walking, running, etc. was investigated. Exposure times were .1 sec to .5 sec.The results reveal that in all Ss the dot pattern is perceptually organized to a gestalt, a walking, running, etc., person at an exposure time of .2 sec. 40% of Ss perceived a human body in such motion at presentation times as short as 0.1 sec. Under the experimental conditions used the track length of the bright spots at the threshold of integration to a moving unit was of the size order 10 visual angle.This result is regarded as indicating that a complex vector analysis of the proximal motion pattern is accomplished at the initial stage of physiological signal recording and that it is a consequence of receptive field organization. It is discussed in terms of vector calculus.     

Visual perception of motion in depth: Application of a vector model to three-dot motion patterns

The aim of the present study was to identify spatial properties of three-dot motion patterns yielding perceived motion in depth. A proposed vector model analyzed each pattern in terms of common and relative motion components of the moving parts. The dots moved in straight paths in a frontoparallel plane. The Ss reported verbally what they perceived. The common motion did not affect the kénd of perceived event (translation or rotation in depth). Relative motions toward or away from a common point, i.e. concurrent motions, yielded perceived translatory motion in depth. Parallel relative motions toward or away from a common line generally yielded perceived rotation in depth. Complex motion patterns, consisting of concurrent and parallel relative motion components combined, evoked simultaneously perceived translation and rotation in depth under certain phase conditions of the components. Some limitations of the model were discussed and suggestions made to widen its generality.     

Alcohol and motion perception

Three motion perception skills were measured under different levels of alcohol ingestion. Our method for detecting decrements in visual information processing proved sensitive to blood alcohol levels as low as .02%. Alcohol in small doses increased reaction times to the onset of motion, particularly to slow speeds, but did not reduce the ability to allocate attention effectively. In view of these findings, certain motion perception tests may be valuable assays for detecting impaired performance with low blood alcohol levels.     

Visual space from visual motion: turn integration in tethered flying Drosophila

Organisms navigating by path integration need to continuously measure their forward movement and their angular orientation with respect to an external reference. How they do it is little understood. Tethered flies at the flight simulator "navigate" in an artificial visual landscape without forward movement. They can return to a previously held orientation if the panorama provides a singularity (landmark) as reference. Surprisingly, in a regularly striped drum without singularities, they can use a temporal cue instead. In this experiment the arena is illuminated with only one color that is either green or blue. The arena is virtually divided into four quadrants. Whenever a quadrant boundary moves past an arbitrary point, the color of the arena light changes. When a fly is heated with one color it acquires a preference for the other one. Subsequently, it avoids the borders toward the potentially 'hot' quadrants even without touching them. The only way to achieve this is by turn integration, that is, by adding and subtracting all the turns it performs once it crosses the border. The color switch defining the border crossing resets the turn integrator, using the orientation of the arena at this moment as reference. In contrast, landmarks or, if it were available, the skylight compass enable the fly to establish by pattern learning any orientation as a reference. If the reference orientation coincides with the desired orientation, that is, if the animal stores the pattern while being oriented toward the goal, it can maintain its orientation without recourse to turn integration (which may be error prone).     

Temporal integration and perception duration

Abstract.— A mathematical model is proposed for the relationship between the intensity of a stimulus as function of time and the intensity of the corresponding respcnse in the form of a conscious experience. The model is based on the assumption that the psychophysical power law is valid for the energy contained in a sliding time-window. The width and shape of this time-window will determine both the region of temporal integration and the perception duration. The consequences of this model are compared with some measurements in hearing and vision, found in the literature.     

Visual perception and corollary discharge

Perception depends not only on sensory input but also on the state of the brain receiving that input. A classic example is perception of a stable visual world in spite of the saccadic eye movements that shift the images on the retina. A long-standing hypothesis is that the brain compensates for the disruption of visual input by using advance knowledge of the impending saccade, an internally generated corollary discharge. One possible neuronal mechanism for this compensation has been previously identified in parietal and frontal cortex of monkeys, but the origin of the necessary corollary discharge remained unknown. Here, we consider recent experiments that identified a pathway for a corollary discharge for saccades that extends from the superior colliculus in the midbrain to the frontal eye fields in the cerebral cortex with a relay in the medial dorsal nucleus of the thalamus. We first review the nature of the evidence used to identify a corollary discharge signal in the complexity of the primate brain and show its use for guiding a rapid sequence of eye movements. We then consider two experiments that show this same corollary signal may provide the input to the frontal cortex neurons that alters their activity with saccades in ways that could compensate for the displacements in the visual input produced by saccadic eye movements. The first experiment shows that the corollary discharge signal is spatially and temporally appropriate to produce the alterations in the frontal-cortex neurons. The second shows that this signal is necessary for this alteration because inactivation of the corollary reduces the compensation by frontal-cortex neurons. The identification of this relatively simple circuit specifies the organization of a corollary discharge in the primate brain for the first time and provides a specific example upon which consideration of the roles of corollary activity in other systems and for other functions can be evaluated.     

Visual perception and aging.

A series of studies performed in our laboratory on aging and its effect on perceptual processing and working memory capacity for visual stimuli are reviewed. Specifically, studies on luminance, colour, motion, texture, and symmetry processing are reported. Furthermore, experiments on the capacity to retain size and spatial frequency information are also discussed. The general conclusion is that there are a number of perceptual abilities that diminish with age. However, the extent of these deficits will depend on the complexity of the neural circuitry involved for processing a given task. This is also true for visual working memory where no evidence of loss due to aging is demonstrated for processing low-level visual information, when individual differences in sensory input are compensated for. It is concluded that perceptual processing deficits due to aging (like working memory) will become evident when the computational load reaches a certain level of complexity (larger or more complex network) even if the tasks remain cognitively simple.     

Visual perception of surface curvature: psychophysics of curvature detection induced by motion parallax

The continuous approach to optic-flow processing shows that the curvature of a moving surface is related to a second spatial derivative of the velocity field, the spin variation (Droulez & Cornilleau-Pérès, 1989). With this approach as a theoretical framework, visual sensitivity to the curvature of a cylinder in motion was measured using a task of discrimination between cylindrical and planar patches. The results confirm the predictions suggested by the theory: (1) Sensitivity to curvature was always greater when the cylinder axis and the frontal translation were parallel than when they were orthogonal. The ratio of curvature detection thresholds in the two cases was between 1.3 and 2.5; the value predicted from the spin variation theory is about 2. (2) Sensitivity to curvature increased strongly with the velocity of the motion but was only weakly affected by its amplitude and the duration of viewing for the range of values used in our experiments.     

Three stimuli for visual motion perception compared

Two arrangements yielding induced motion were used to explore the relative effectiveness of three stimulus conditions known to produce perception of motion—namely, image displacement, ocular pursuit, and object-relative displacement. In these arrangements, object-relative displacement, which resulted in induced motion, was in conflict either with ocular pursuit or with image displacement. The outcomes of these conflicts were determined by measuring the extent of induced motion. Image displacement proved more effective in competing with object-relative displacement than did ocular pursuit, which in one arrangement yielded to object-relative displacement entirely. The same pattern of results was obtained both with the usual arrangement of the moving-center type and with a stationary-center display.     

Visual perception of markings

Markings, such as designs, writings, diagrams, and depictions, are expressive and communicative human artifacts. The conventional assumption that findings from the study of the visual perception of markings—in particular, of pictures—can be generalized to real-world perception is examined and found to be false. The processes involved in the visual perception of the world and in the visual perception of markings differ in significant ways, and generalizations from one to the other must be undertaken with caution. The visual perception of markings is an identifiable and separate area of study. Implications for a general theory of the perception of markings are examined, and the perception of markings is contrasted with real-world perception.     

Visual perception of collinearity

In a metrical space, there exists an intimate relation between collinearity and parallelity. In particular, in a Riemannian space collinearity is just a special case of parallelity. Is this true for visual space as well? We investigated the visual perception of collinearity by having subjects align two bars in the horizontal plane at eye height. The distances of the bars from the subject and the angles at which they were placed were varied. We found deviations of up to 22 degrees. The deviations of the left and right bars could be split into two independent components: namely, the sum and the difference of the deviations of the left and right bars. We found that the former depended only on the ratio between the distances of each bar from the subject, whereas the latter was largely independent of the positions of the bars. The difference in deviations corresponded to the deviation from parallelity. Compared with the results in the parallelity task (Cuijpers, Kappers, & Koenderink, 2000b), the deviations from parallel were much smaller. As a consequence, the results of the two experiments cannot be described by the same Riemannian geometry. This indicates that the intrinsic geometry of visual space differs across tasks. This is conceivable if the intrinsic geometry of visual space is operationally defined.     

Visual motion and attentional capture

Previous work has shown that abrupt visual onsets capture attention. This occurs even with stimuli that are equiluminant with the background, which suggests that the appearance of a new perceptual object, not merely a change in luminance, captures attention. Three experiments are reported in which this work was extended by investigating the possible role of visual motion in attentional capture. Experiment 1 revealed that motion can efficiently guide attention when it is perfectly informative about the location of a visual search target, but that it does not draw attention when it does not predict the target’s position. This result was obtained with several forms of motion, including oscillation, looming, and nearby moving contours. To account for these and other results, we tested anew-object account of attentional capture in Experiment 2 by using a global/local paradigm. When motion segregated a local letter from its perceptual group, the local letter captured attention as indexed by an effect on latency of response to the task-relevant global configuration. Experiment 3 ruled out the possibility that the motion in Experiment 2 captured attention merely by increasing the salience of the moving object. We argue instead that when motion segregates a perceptual element from a perceptual group, a new perceptual object is created, and this event captures attention. Together, the results suggest that motion as such does not capture attention but that the appearance of a new perceptual object does.     

Visual perception of biological motion in newly hatched chicks as revealed by an imprinting procedure

Day-old chicks were exposed to point-light animation sequences depicting either a walking hen or a rotating cylinder. On a subsequent free-choice test (experiment 1) the chicks approached the novel stimulus, irrespective of this being the hen or the cylinder. In order to obtain equivalent local motion vectors, in experiments 2 and 3 newly hatched chicks were exposed either to a point-light animation sequence depicting a walking hen, or to a positionally scrambled walking hen (i.e. an animation in which exactly the same set of dots in motion as that employed for the walking hen was presented, but with spatially randomized starting positions). Chicks tested on day 1 (experiment 2) or on day 2 (i.e. after a period in the dark following exposure on day 1 (experiment 3)) proved able to discriminate the two animation sequences: males preferentially approached the novel stimulus, females the familiar one. These results indicate that discrimination was not based on local motion vectors, but rather on the temporally integrated motion sequence. Received: 18 August 1999 / Accepted after revision: 14 March 2000