The role of eye movements in the perception of visually induced autokinesis

Changes in eye position were recorded physiologically while S experienced visually induced autokinesis. Eye movements did not seem to sufficiently explain this phenomenon. Apparent motion was found to be based upon a change in phenomenal rather than retinal location. Special consideration was given to those parameters possibly responsible for paradoxical motion.     

The role of attention in the preparation of visually guided eye movements in monkey and man

Summary Neurophysiological data from single cells in the monkey's visual association cortex as well as saccadic reaction time measurements in monkey and man are reported. When a monkey directs his attention to a peripheral light stimulus the visual activation of cortical cells responsive to that stimulus is increased. If visual attention is directed to a particular part of the visual field the saccadic reaction time is long (around 200 ms in monkey and above 200 ms in man). In contrast, if attention is disengaged from any location to which it might have been engaged before, monkeys and men can execute express saccades, that is, saccades after extremely short and stable reaction times (around 75 ms in monkey and 100 ms in man). The results are interpreted in the context of a hypothesis according to which the initiation of voluntary, visually guided saccades includes three premotor mechanisms: the computation of the target location, the decision to make a saccade, and the disengagement of attention.     

Tracking without perceiving: a dissociation between eye movements and motion perception

Can people react to objects in their visual field that they do not consciously perceive? We investigated how visual perception and motor action respond to moving objects whose visibility is reduced, and we found a dissociation between motion processing for perception and for action. We compared motion perception and eye movements evoked by two orthogonally drifting gratings, each presented separately to a different eye. The strength of each monocular grating was manipulated by inducing adaptation to one grating prior to the presentation of both gratings. Reflexive eye movements tracked the vector average of both gratings (pattern motion) even though perceptual responses followed one motion direction exclusively (component motion). Observers almost never perceived pattern motion. This dissociation implies the existence of visual-motion signals that guide eye movements in the absence of a corresponding conscious percept.     

Disruption of eye movements by ethanol intoxication affects perception of depth from motion parallax

Motion parallax, the ability to recover depth from retinal motion generated by observer translation, is important for visual depth perception. Recent work indicates that the perception of depth from motion parallax relies on the slow eye movement system. It is well known that ethanol intoxication reduces the gain of this system, and this produces the horizontal gaze nystagmus that law enforcement's field sobriety test is intended to reveal. The current study demonstrates that because of its influence on the slow eye movement system, ethanol intoxication impairs the perception of depth from motion parallax. Thresholds in a motion parallax task were significantly increased by acute ethanol intoxication, whereas thresholds for an identical test relying on binocular disparity were unaffected. Perhaps a failure of motion parallax plays a role in alcohol-related driving accidents; because of the effects of alcohol on eye movements, intoxicated drivers may have inaccurate or inadequate information for judging the relative depth of obstacles from motion parallax.     

Vergence eye movements during figure-ground perception

Figure-ground, that is the segmentation of visual information into objects and their surrounding backgrounds, provides structure for visual attention. Recent evidence shows a novel role of vergence eye movements in visual attention. In the present work, vergence responses during figure-ground segregation tasks are psychophysically investigated. We show that during a figure-ground detection task, subjects convergence their eyes. Vergence eye movements are larger in figure trials than in ground trials. In detected figures trials, vergence are stronger than in trials where the figure went unnoticed. Moreover in figure trials, vergence responses are stronger to low-contrast figures than to high-contrast figures. We argue that these discriminative vergence responses have a role in figure-ground.     

The influence of eye movements and eye position on perception of the visual vertical

Summary Four experiments are reported which involved the adjustment of two points of light in an otherwise dark room to the visual vertical. In the first two experiments different point separations (corresponding to visual angles of about 2° and 23°) were employed in an attempt to control the degree of scanning eye movements. Binocular adjustments to the visual vertical during body tilt were influenced by the point separation (Exp. 1), but monocular adjustments with the head upright were not (Exp. 2). Using the larger point separation and fixating the top point the visual vertical using the right eye was counterclockwise of that with fixation of the bottom point when the head was upright (Exp. 3), but this difference was not found for judgments during tilt (Exp. 4). The results were discussed in terms of the rotational changes in eye position accompanying scanning eye movements and ocular elevation and depression.

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Zusammenfassung Es wird über vier Experimente berichtet, in denen es um die Einstellungen zweier Lichtpunkte in eine vertikale Richtung geht. In den ersten zwei Experimenten sollte der Einfluß der Fixierbewegungen der Augen geprüft werden. Der Winkelabstand der Lichtpunkte betrug 2° oder 23°. Bei seitwärts geneigtem Körper und binokularer Betrachtung wurde ein Unterschied gefunden (Exp. 1). Bei aufrecht gehaltenem Kopf und monokularer Betrachtung dagegen zeigte sich kein Unterschied (Exp. 2). Wurde in aufrechter Körperlage und bei einem Punktabstand von 23° der obere Punkt mit dem rechten Auge fixiert, so verschob sich die scheinbare Vertikale im Uhrzeigersinn; sie verschob sich noch weiter im Uhrzeigersinn, wenn der untere Punkt fixiert wurde (Exp. 3). Bei geneigtem Körper wurde dagegen kein Unterschied festgestellt (Exp. 4). Die Ergebnisse werden im Zusammenhang mit der Augendrehung diskutiert, die mit dem scanning sowie mit der Auf- und Abbewegung der Augen beim Fixieren verbunden ist.

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This research was carried out while I was a recipient of a Forschungsstipendium from the Alexander von Humboldt-Stiftung, appreciation for which is gratefully acknowledged. I also wish to thank the subjects who participated in the experiments.     

Coordination of eye and leg movements during visually guided stepping

In the present study, 2 related hypotheses were tested: first, that vision is used in a feedforward control mode during precision stepping onto visual targets and, second, that the oculomotor and locomotor control centers interact to produce coordinated eye and leg movements during that task. Participants' (N = 4) eye movements and step cycle transition events were monitored while they performed a task requiring precise foot placement at every step onto irregularly placed stepping stones under conditions in which the availability of visual information was either restricted or intermittently removed altogether. Accurate saccades, followed by accurate steps, to the next footfall target were almost always made even when the information had been invisible for as long as 500 ms. Despite delays in footlift caused by the temporary removal (and subsequent reinstatement) of visual information, the mean interval between the start of the eye movement and the start of the swing toward a target did not vary significantly (p >.05). In contrast, the mean interval between saccade onset away from a target and a foot landing on that target (stance onset) did vary significantly (p <.05) under the different experimental conditions. Those results support the stated hypotheses.     

The flash-lag phenomenon: object motion and eye movements

An object flashed briefly in a given location, the moment another moving object arrives in the same location, is perceived by observers as lagging behind the moving object (flash-lag effect). Does the flash-lag effect occur if the retinal image of the moving object is rendered stationary by smooth pursuit of the moving object? Does the flash-lag effect occur if the retinal image of a stationary object is caused to move by smooth-pursuit eye movements? A disk was briefly flashed in the center of a moving ring such that the ring center was completely 'filled' by the disk. In this display, observers perceived the flashed disk to lag such that it appeared only to partially 'fill' the ring center. The 'unfilled' portion (perceived void) of the moving ring was seen in the color of the background. With smooth pursuit of the ring, the flash-lag effect was eliminated, and observers saw the flashed disk centered on the moving ring. A strong flash-lag effect was observed when observers smoothly pursued a moving point target past a continuously visible stationary ring. Once again, the flashed disk appeared to only partially fill the center of the continuously visible stationary ring, yielding a vivid 'perceived void'. These results are discussed in terms of neural delays and their compensation.     

The role of eye movements in subitizing and counting

Previous work has suggested that eye movements may be necessary for accurate enumeration beyond the subitization range of about 4 items. This study determined the frequency of eye movements normally made during enumeration, their relationship to response times, and whether they are required for accurate performance. This was achieved by monitoring eye movements and comparing performance when observers were allowed to saccade and when they were not. The results showed that (a) there was a sharp increase in saccadic frequency beyond about 4 items (from < 0.2 saccades per item to about 1 per item), and (b) enumeration of fewer than 4 items remained rapid and accurate even when eye movements were prevented, whereas enumeration beyond this became less efficient and sometimes less accurate. The results are discussed in relation to the memory and processing requirements of enumeration tasks.     

The role of visual attention in saccadic eye movements

The relationship between saccadic eye movements and covert orienting of visual spatial attention was investigated in two experiments. In the first experiment, subjects were required to make a saccade to a specified location while also detecting a visual target presented just prior to the eye movement. Detection accuracy was highest when the location of the target coincided with the location of the saccade, suggesting that subjects use spatial attention in the programming and/or execution of saccadic eye movements. In the second experiment, subjects were explicitly directed to attend to a particular location and to make a saccade to the same location or to a different one. Superior target detection occurred at the saccade location regardless of attention instructions. This finding shows that subjects cannot move their eyes to one location and attend to a different one. The results of these experiments suggest that visuospatial attention is an important mechanism in generating voluntary saccadic eye movements.     

The role of eye movements in motor sequence learning

An experiment that utilized a 16-element movement sequence was designed to determine the impact of eye movements on sequence learning. The participants were randomly assigned to two experimental groups: a group that was permitted to use eye movements (FREE) and a second group (FIX) that was instructed to fixate on a marker during acquisition (ACQ). A retention test (RET) was designed to provide a measure of learning, and two transfer tests were designed to determine the extent to which eye movements influenced sequence learning. The results demonstrated that both groups decreased the response time to produce the sequence, but the participants in the FREE group performed the sequence more quickly than participants of the FIX group during the ACQ, RET and the two transfer tests. Furthermore, continuous visual control of response execution was reduced over the course of learning. The results of the transfer tests indicated that oculomotor information regarding the sequence can be stored in memory and enhances response production.     

Adaptation in motion perception: Alteration of induced motion

Prolonged exposure to a condition that causes induced motion was found to diminish this effect. The extent of a horizontal induced motion was measured by obtaining estimates of the direction of the apparent oblique path that resulted when a spot was visible on a horizontally moving pattern and was therefore in horizontal induced motion and, at the same time, moved vertically. Because the horizontal component of the perceived motion path represented the induced motion, the slope of the path measured the extent of the induced motion. After a 10-min exposure to induced motion, the apparent motion path was steeper; the mean change corresponded to a 15% smaller extent of the induced motion. Results were obtained that argue that this effect is not due to a diminished horizontal motion of the pattern but amounts to a smaller motion-inducing effect. The experiments were meant to support the view that the perceptual process that underlies induced motion is learned.     

The role of the saccade target object in the perception of a visually stable world

Although the proximal stimulus shifts position on our retinae with each saccade, we perceive our world as stable and continuous. Most theories of visual stability implicitly assume a mechanism that spatially adjusts perceived locations associated with the retinal array by using, as a parameter, extra-retinal eye position information, a signal that encodes the size and direction of the saccade. The results from the experiment reported in this article challenge this idea. During a participant's saccade to a target object, one of the following was displaced: the entire scene, the target object, or the background behind the target object. Participants detected the displacement of the target object twice as frequently as the displacement of the entire background. The direction of displacement relative to the saccade also affected detectability. We use a new theory, the saccade target theory (McConkie & Currie, 1996), to interpret these results. This theory proposes that retinal (as opposed to extra-retinal) factors, primarily those concerning the saccade target object, are critical for the detection of intrasaccadic stimulus shifts.     

The role of motion in infants' perception of solid shape

Previous research has shown that infants as young as the first few months of life perceive several aspects of the three-dimensional environment. Yet we know relatively little about the visual depth information which serves as a basis for their spatial capacities. A study is reported in which a visual habituation procedure was used to examine what types of optical depth information four-month-old infants find useful in visually perceiving solid (three-dimensional) shape. Results imply that in the absence of binocular depth cues four-month-olds rely on kinetic depth information to perceive solid shape.