Perceived movement of the afterimage during eye movements

The question of whether an afterimage viewed in a dark field appears to move during eye movement was studied by comparing recordings of eye movements with recordings of reports of perceived movement. The correlation was found to be quite good even under conditions where the eye movements were spontaneous rather than specifically directed. The results were taken to support the hypothesis that the behavior of the retinal image is “interpreted” by taking into account information concerning what the eyes are doing.     

Apparent motion of stimuli presented stroboscopically during pursuit movement of the eye

This paper reports the first phase of a research program on visual perception of motion patterns characteristic of living organisms in locomotion. Such motion patterns in animals and men are termed here as biological motion. They are characterized by a far higher degree of complexity than the patterns of simple mechanical motions usually studied in our laboratories. In everyday perceptions, the visual information from biological motion and from the corresponding figurative contour patterns (the shape of the body) are intermingled. A method for studying information from the motion pattern per se without interference with the form aspect was devised. In short, the motion of the living body was represented by a few bright spots describing the motions of the main joints. It is found that 10–12 such elements in adequate motion combinations in proximal stimulus evoke a compelling impression of human walking, running, dancing, etc. The kinetic-geometric model for visual vector analysis originally developed in the study of perception of motion combinations of the mechanical type was applied to these biological motion patterns. The validity of this model in the present context was experimentally tested and the results turned out to be highly positive.     

Apparent haptic movement

When Os were presented with ISO-Hz vibrotactile bursts at two loci on the skin of the thigh and permitted to adjust the time between burst onsets, they reported good apparent movement between the loci. The time between stimulus onsets for optimal movement was found to vary directly with the duration of the stimulus. Replication of the experiment with electrocutaneous stimuli at 1 KHz yielded similar results. Comparison of the data with results from a study of visual apparent movement revealed no difference between the two modalities for the relationship between stimulus onset intervals and stimulus duration. The significance of the results for hypotheses about the processes underlying perception of apparent movement is discussed.     

Apparent haptic movement

When as were presented with 150-Hz vibrotactile bursts at two loci on the skin of the thigh and permitted to adjust the time between burst onsets, they reported good apparent movement between the loci. The time between stimulus onsets for optimal movement was found to vary directly with the duration of the stimulus. Replication of the experiment with electrocutaneous stimuli at 1 KHz yielded similar results. Comparison of the data with results from a study of visual apparent movement revealed no difference between the two modalities for the relationship between stimulus onset intervals and stimulus duration. The significance of the results for hypotheses about the processes underlying perception of apparent movement is discussed.     

Eye movements drive steering: reduced eye movement distribution impairs steering and driving performance

On a winding open road, a driver consistently looks to the inside of each bend before turning the steering wheel. When researchers disrupt this coordination by instructing drivers not to move their eyes, drivers' performance is impaired and their completion time during racing increases. The present authors examined whether changing internal states in a way that also restricts eye movements reduces coordination and affects performance. Participants (N = 24) completed a simulated rally stage under manipulation of their anxiety state through ego threat. Performance decreased under pressure, and the decrement was associated with a narrowing of the range of eye movements and a reduced correlation of eye movements with steering. The authors discuss the possibility that the deterioration in performance is a cost of maintaining steering when eye-movement driving input to the steering controller is reduced.     

Induced rotary movement during eye movements: displays with unequal spacing of pattern

In my previous (Reinhardt-Rutland, 1982) study, I suggested that eye movements enhance induced rotary movement. However, low salience of absolute displacement might also explain the results, as displays were covered with large numbers of equally spaced radial pattern elements. To test these competing hypotheses in the present study, I used an unequally spaced pattern in two displays. Common to each display was an annulus: In one display, the common annulus surrounded a disk, and in the other display the common annulus was surrounded by another annulus. In any trial, one component rotated and the other was stationary while for 40 s the subject's eyes followed a circular path concentric with the display; subjects timed those occasions when perceived stronger rotation resided in the common annulus. Despite an unequally spaced pattern, absolute displacement had a barely significant effect. Instead, perceived stronger rotation mostly resided in a display's more central component. I concluded therefore that eye movements enhance induced rotary movement.     

Apparent movement and the Brown-Voth experiment

An experiment on apparent movement reported by Brown and Voth and referred to by Osgood and Bartley was repeated. The results obtained differed from those reported by Brown and Voth, but exhibited phenomena not described by them. Further experiments derived from their theories were also carried out, the results failing to support Korte's laws and raising some new points.     

Apparent movement induced by afterimages

A small light source viewed in the dark through an afterimage produced by an electronic flash may appear to move along short random paths. Experiment 1 shows that this is not an instance of the autokinetic phenomenon, and experiment 2 shows that it is not related to the 'fluttering hearts' phenomenon. On the basis of experiments 1 and 3 it is concluded that small-scale ocular drifts, microsaccades, and possibly tremors cause the whole afterimage to move. The afterimage serves as a frame of reference and induces movement of the light source.     

Apparent movement in tridimensional space

The space-time relationships satisfying Korte’s third law of apparent movement were studied in three experiments. The results generally confirm and extend Corbin’s conclusion that apparent movement is not a projection-level phenomenon, but one involving spatial constancy, i.e., some representation of tridimensional space. Between situations in which the stimuli were retinally matched, the time interval necessary, for apparent movement varied w~th their phenomenal separation, whether the latter was determined by the distance of stimuli from the O, deviation of sttmuli from the frontal plane, or illusory slant of the stimulus plane produced by a perspective gradient.     

Apparent movement in phenomenal space

The spatial and temporal variables in Korte’s third law of apparent movement were studied in pictorial arrays in which size constancy could be expected to prevail. The thresholds for apparent movement were determined under conditions in which two squares appeared on a plane either with or without perspective information for depth. The results suggest that apparent movement varies with the perceived depth separation only if the size of the stimulus pair is congruent with contextual depth representations. The obtained psychophysical function relating thresholds for third-dimensional movement to pictorial depth scale supports the view that apparent movement preserves gradient-of-texture information.     

Attention and saccadic eye movements

Four threshold detection experiments addressed three issues concerning the relationship between movements of spatial attention and saccadic eye movements: (a) the time course of attention shifts wit saccades, (b) the response of the two systems to changes in stimulus parameters, and (c) the relationship of attention to saccadic suppression. These issues bear on the more general question of the degree of independence between the saccadic and attentional movement systems. The results of these experiments support the contention that the mechanisms that shift attention are separate from those that control saccadic eye movements. Relevant events in the visual field periphery, however, will trigger both a saccade and attention shift. The attentional response to such events does not appear to be under subjects' control. The implication of these results for theories of saccadic suppression is discussed.     

Programming saccadic eye movements

This article addresses questions about the preparatory processes that immediately precede saccadic eye movements. Saccade latencies were measured in a task in which subjects were provided partial advance information about the spatial location of a target fixation. In one experiment, subjects were faster in initiating saccades when they knew either the direction or amplitude of the required movement in advance compared to a condition with equal uncertainty about the number of potential saccade targets but without knowledge of the parameters required to execute the movement. These results suggest that the direction and amplitude for an upcoming saccade were calculated separately, and not in a fixed serial order. In another experiment, subjects appear to have programmed the saccades more holistically--with computations of direction and amplitude parameters occurring simultaneously. The implications of these results for models of eye movement preparation are discussed.     

Is target movement as well as target displacement a stimulus for saccadic eye movements?

The effects of visual movement on saccadic eye movement have been examined. In a classic apparent-movement demonstration with two successively exposed line-segment targets the quality of the movement is dependent on the relative orientation of the line segments. If saccadic eye movements are elicited between the targets in this situation, the configuration leading to optimal apparent movement also leads to the shortest-latency saccades. When a single line segment is succeeded by two line segments flanking it on opposite sides, and if one of these has the same orientation as the initial one and the other a different orientation, then apparent motion is seen between the two lines with the same orientation. However, the direction of saccades elicited in this configuration is not influenced by the relative orientations of the line segments. The two results together suggest that the effect of visual movement on saccadic eye movement is nonspecific.     

Apparent movement detection in the pigeon

Pigeons were trained to discriminate between the presence and absence of apparent movement in visual displays. Generalization gradients obtained on the dimension of speed indicated a broad range of movement detection. Extremely accurate discrimination performance on displays varying in direction of movement suggested formation of a "movement concept".     

Dyslexic and normal readers' eye movements

Dyslexic and normal readers' eye movements were compared while tracking a moving fixation point and in reading. Contrary to previous reports, the dyslexic and normal readers did not differ in their number of saccades, percentage of regressions, or stability of fixations in the tracking task. Thus, defective oculomotor control was not associated with or a causal factor in dyslexia, and the dyslexics' abnormal eye movements in reading must be related to differences in higher cognitive processes. However, individual differences in oculmotor efficiency, independent of reading ability, were found within both the dyslexic and normal groups, and these differences were correlated in reading and tracking tasks.     

Saccadic eye movements and dual-task interference

Four dual-task experiments required a speeded manual choice response to a tone in a close temporal proximity to a saccadic eye movement task. In Experiment 1, subjects made a saccade towards a single transient; in Experiment 2, a red and a green colour patch were presented to left and right, and the saccade was to which ever patch was the pre-specified target colour. There was some slowing of the eye movement, but neither task combination showed typical dual-task interference (the “psychological refractory effect”). However, more interference was observed when the direction of the saccade depended on whether a central colour patch was red or green, or when the saccade was directed towards the numerically higher of two large digits presented to the left and the right. Experiment 5 examined a vocal second task, for comparison. The findings might reflect the fact that eye movements can be directed by two separate brain systems--the superior colliculus and the frontal eye fields; commands from the latter but not the former may be delayed by simultaneous unrelated sensorimotor tasks.     

Saccadic eye movements and reading difficulties

Saccadic eye movements of 14 children with reading difficulties and of 14 normal readers were compared before and after the problem readers underwent a seven month individual tutoring program. At pretesting the problem readers showed a rate of eye movements that was markedly lower than that of the normal readers whose rate they attained and surpassed at completion of the remedial reading program. Results are discussed in terms of the presumed function of saccadic eye movements and their relation to reading, attention, and information gathering.This study was supported by grant OEG-2-2-2BO24 from the National Institute of Education. The valuable assistance of Mark J. Fischer and the help of Sandra Armel, Steven Rayack, and Betty White are gratefully acknowledged. Dr. Lowey, of the Three Village School District and particularly Mr. Hanrahan, Principal of Main Street School, greatly facilitated our work and we are most grateful.