scholarly journals Saccadic Behavior during the Response to Pure Vergence Stimuli I: General Properties

2007 ◽  
Vol 1 (2) ◽  
Author(s):  
John Semmlow ◽  
Yung-Fu Chen ◽  
Tara L. Alvarez ◽  
Claude Pedrono
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
Saccadic Eye Movements ◽  
Stimulus Onset ◽  
The Other ◽  
General Properties ◽  
Dominant Eye ◽  
Vergence Movement ◽  
The Asymmetry ◽  
Almost All

If two targets are carefully aligned so that they fall along the cyclopean axis, the required eye movement will be symmetrical with the two eyes turning equally inward or outward. When such “pure vergence stimuli” are used only a “pure vergence movement” is required, yet almost all responses include saccadic eye movements, a rapid tandem movement of the eyes. When saccades occur, they must either produce an error in the desired symmetrical response or correct an error from an asymmetrical vergence response. A series of eye movement responses to pure convergence stimuli (4.0 deg step stimuli) were measured in 12 subjects and the occurrence, timing and amplitude of saccades was measured. Early saccades (within 400 msec of the stimulus onset) appeared in 80% to 100% of the responses. In most subjects, the first saccade increased the asymmetry of the response, taking the eyes away from the midline position. In three subjects, these asymmetry-inducing saccades brought one eye, the preferred or dominant eye, close to the target, but in the other subjects these asymmetry-inducing saccades were probably due to the distraction caused by the transient diplopic image generated by a pure vergence stimulus. While many of these asymmetry-inducing saccades showed saccade-like enhancements of vergence, they were, with the exception of two subjects, primarily divergent and did not facilitate the ongoing convergence movement. All subjects had some responses where the first saccade improved response symmetry, correcting an asymmetry brought about by unequal vergence movements in the two eyes. In five subjects, large symmetry-inducing saccades corrected an asymmetrical vergence response, bringing the eyes back to the midline (to within a few tenths of a degree).

scholarly journals Time course of spatiotopic updating across saccades

2019 ◽  
Vol 116 (6) ◽  
pp. 2027-2032 ◽  
Author(s):  
Jasper H. Fabius ◽  
Alessio Fracasso ◽  
Tanja C. W. Nijboer ◽  
Stefan Van der Stigchel
Keyword(s):  
Eye Movements ◽  
Visual System ◽  
Eye Movement ◽  
Time Course ◽  
Saccadic Eye Movements ◽  
Oculomotor System ◽  
Stimulus Onset ◽  
Oculomotor Behavior ◽  
Behavioral Studies ◽  
The Brain

Humans move their eyes several times per second, yet we perceive the outside world as continuous despite the sudden disruptions created by each eye movement. To date, the mechanism that the brain employs to achieve visual continuity across eye movements remains unclear. While it has been proposed that the oculomotor system quickly updates and informs the visual system about the upcoming eye movement, behavioral studies investigating the time course of this updating suggest the involvement of a slow mechanism, estimated to take more than 500 ms to operate effectively. This is a surprisingly slow estimate, because both the visual system and the oculomotor system process information faster. If spatiotopic updating is indeed this slow, it cannot contribute to perceptual continuity, because it is outside the temporal regime of typical oculomotor behavior. Here, we argue that the behavioral paradigms that have been used previously are suboptimal to measure the speed of spatiotopic updating. In this study, we used a fast gaze-contingent paradigm, using high phi as a continuous stimulus across eye movements. We observed fast spatiotopic updating within 150 ms after stimulus onset. The results suggest the involvement of a fast updating mechanism that predictively influences visual perception after an eye movement. The temporal characteristics of this mechanism are compatible with the rate at which saccadic eye movements are typically observed in natural viewing.

scholarly journals A Fast and Effective System for Analysis of Optokinetic Waveforms with a Low-Cost Eye Tracking Device

Healthcare ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 10
Author(s):  
Chong-Bin Tsai ◽  
Wei-Yu Hung ◽  
Wei-Yen Hsu
Keyword(s):  
Eye Movements ◽  
Eye Tracking ◽  
Eye Movement ◽  
Low Cost ◽  
Saccadic Eye Movements ◽  
Slow Phase ◽  
Eye Tracker ◽  
Effective System ◽  
Tracking Device ◽  
Traditional Approaches

Optokinetic nystagmus (OKN) is an involuntary eye movement induced by motion of a large proportion of the visual field. It consists of a “slow phase (SP)” with eye movements in the same direction as the movement of the pattern and a “fast phase (FP)” with saccadic eye movements in the opposite direction. Study of OKN can reveal valuable information in ophthalmology, neurology and psychology. However, the current commercially available high-resolution and research-grade eye tracker is usually expensive. Methods & Results: We developed a novel fast and effective system combined with a low-cost eye tracking device to accurately quantitatively measure OKN eye movement. Conclusions: The experimental results indicate that the proposed method achieves fast and promising results in comparisons with several traditional approaches.

Phantom array and stroboscopic effects of a time-modulated moving light source during saccadic eye movement

2017 ◽  
Vol 50 (5) ◽  
pp. 772-786 ◽  
Author(s):  
C-S Lee ◽  
J-H Lee ◽  
H Pak ◽  
SW Park ◽  
D-W Song
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
Light Source ◽  
Light Emitting Diode ◽  
Saccadic Eye Movements ◽  
Movement Speed ◽  
Light Sources ◽  
Saccadic Eye Movement ◽  
Modulated Light ◽  
Source Motion

This paper evaluates the detectability of the phantom array and stroboscopic effects during light source motion, eye movement and their combination, using time modulated light-emitting diode light sources. It is well known that the phantom array can be observed when time-modulated light sources are observed during saccadic eye movements. We investigated whether light source motion can cause similar effects when the subject has fixed eyes. In addition, we estimated the detectability threshold frequency for the combination of stroboscopic effect and the phantom array, which is named the stroboscopic-phantom array effect, during two eye movements in opposite directions under one directional rotating light source with variable speed. Our results indicate that one of the most important factors for the stroboscopic-phantom array effect is eye movement speed relative to the speed of the light source. Therefore, time-modulated moving light sources induce a stroboscopic effect in subjects with fixed eyes that is similar to the stroboscopic-phantom array effect observed during saccadic eye movement. Our findings are likely to be useful for predicting the stroboscopic effect and the stroboscopic-phantom array effect during the fast motion of time-modulated LED light sources, like multi-functional rear lamps, in automotive lighting applications.

Sleeping Pills and Dream Content

1974 ◽  
Vol 124 (583) ◽  
pp. 547-553 ◽  
Author(s):  
Hugh Firth
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
Rem Sleep ◽  
Normal Values ◽  
Dream Content ◽  
Rapid Eye Movement ◽  
Sleeping Pills ◽  
Almost All ◽  
Natural Pattern

Almost all sleep-promoting drugs distort the natural pattern of sleep by suppressing rapid eye movement (REM) sleep, and cause a rebound to above-normal values on withdrawal which typically lasts about six weeks (Oswald, 1968, 1969). Furthermore, barbiturates reduce the number of eye movements per unit time in REM sleep (Oswald et al., 1963; Baekeland, 1967; Lester et al., 1968; Feinberg et al., 1969), with a rebound in eye movement (EM) profusion on withdrawal (Oswald, 1970). Non-barbiturate hypnotics do likewise, also with a rebound in EM profusion on withdrawal (Allen et al., 1968; Lewis, 1968).

Effects of Viewing Distance on the Responses of Vestibular Neurons to Combined Angular and Linear Vestibular Stimulation

1999 ◽  
Vol 81 (5) ◽  
pp. 2538-2557 ◽  
Author(s):  
Chiju Chen-Huang ◽  
Robert A. McCrea
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
Vestibular Stimulation ◽  
The Other ◽  
Viewing Distance ◽  
Vestibuloocular Reflex ◽  
Horizontal Canal ◽  
Head Velocity ◽  
Vestibular Neurons ◽  
Axis Of Rotation

Effects of viewing distance on the responses of vestibular neurons to combined angular and linear vestibular stimulation. The firing behavior of 59 horizontal canal–related secondary vestibular neurons was studied in alert squirrel monkeys during the combined angular and linear vestibuloocular reflex (CVOR). The CVOR was evoked by positioning the animal’s head 20 cm in front of, or behind, the axis of rotation during whole body rotation (0.7, 1.9, and 4.0 Hz). The effect of viewing distance was studied by having the monkeys fixate small targets that were either near (10 cm) or far (1.3–1.7 m) from the eyes. Most units (50/59) were sensitive to eye movements and were monosynaptically activated after electrical stimulation of the vestibular nerve (51/56 tested). The responses of eye movement–related units were significantly affected by viewing distance. The viewing distance–related change in response gain of many eye-head-velocity and burst-position units was comparable with the change in eye movement gain. On the other hand, position-vestibular-pause units were approximately half as sensitive to changes in viewing distance as were eye movements. The sensitivity of units to the linear vestibuloocular reflex (LVOR) was estimated by subtraction of angular vestibuloocular reflex (AVOR)–related responses recorded with the head in the center of the axis of rotation from CVOR responses. During far target viewing, unit sensitivity to linear translation was small, but during near target viewing the firing rate of many units was strongly modulated. The LVOR responses and viewing distance–related LVOR responses of most units were nearly in phase with linear head velocity. The signals generated by secondary vestibular units during voluntary cancellation of the AVOR and CVOR were comparable. However, unit sensitivity to linear translation and angular rotation were not well correlated either during far or near target viewing. Unit LVOR responses were also not well correlated with their sensitivity to smooth pursuit eye movements or their sensitivity to viewing distance during the AVOR. On the other hand there was a significant correlation between static eye position sensitivity and sensitivity to viewing distance. We conclude that secondary horizontal canal–related vestibuloocular pathways are an important part of the premotor neural substrate that produces the LVOR. The otolith sensory signals that appear on these pathways have been spatially and temporally transformed to match the angular eye movement commands required to stabilize images at different distances. We suggest that this transformation may be performed by the circuits related to temporal integration of the LVOR.

Providing a human user artificial ability to control their eyes independently with various eye movement patterns

2012 ◽  
Vol 25 (0) ◽  
pp. 171-172
Author(s):  
Fumio Mizuno ◽  
Tomoaki Hayasaka ◽  
Takami Yamaguchi
Keyword(s):  
Eye Movements ◽  
Visual Perception ◽  
Control Systems ◽  
Eye Movement ◽  
Binocular Rivalry ◽  
Human Visual System ◽  
Visual Stimulation ◽  
The Other ◽  
Flexible Adaptation ◽  
Left And Right

Humans have the capability to flexibly adapt to visual stimulation, such as spatial inversion in which a person wears glasses that display images upside down for long periods of time (Ewert, 1930; Snyder and Pronko, 1952; Stratton, 1887). To investigate feasibility of extension of vision and the flexible adaptation of the human visual system with binocular rivalry, we developed a system that provides a human user with the artificial oculomotor ability to control their eyes independently for arbitrary directions, and we named the system Virtual Chameleon having to do with Chameleons (Mizuno et al., 2010, 2011). The successful users of the system were able to actively control visual axes by manipulating 3D sensors held by their both hands, to watch independent fields of view presented to the left and right eyes, and to look around as chameleons do. Although it was thought that those independent fields of view provided to the user were formed by eye movements control corresponding to pursuit movements on human, the system did not have control systems to perform saccadic movements and compensatory movements as numerous animals including human do. Fluctuations in dominance and suppression with binocular rivalry are irregular, but it is possible to bias these fluctuations by boosting the strength of one rival image over the other (Blake and Logothetis, 2002). It was assumed that visual stimuli induced by various eye movements affect predominance. Therefore, in this research, we focused on influenced of patterns of eye movements on visual perception with binocular rivalry, and implemented functions to produce saccadic movements in Virtual Chameleon.

Saccadic Eye Movements and Dual-Task Interference

1993 ◽  
Vol 46 (1) ◽  
pp. 51-82 ◽  
Author(s):  
Harold Pashler ◽  
Mark Carrier ◽  
James Hoffman
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
Dual Task ◽  
Saccadic Eye Movements ◽  
Choice Response ◽  
Task Interference ◽  
The Right ◽  
Colour Patch ◽  
Dual Task Interference ◽  
Close Temporal Proximity

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.

Visual Fatigue and Saccadic Eye Movement Parameters

1983 ◽  
Vol 27 (8) ◽  
pp. 728-732 ◽  
Author(s):  
Ted Megaw ◽  
Tayyar Sen
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
Peak Velocity ◽  
Cognitive Task ◽  
Saccadic Eye Movements ◽  
Tracking Task ◽  
Frequency Of Occurrence ◽  
Saccadic Eye Movement ◽  
Visual Fatigue ◽  
Movement Parameters

It has been suggested by Bahill and Stark (1975) that visual fatigue can be identified by changes in some of the saccadic eye movement parameters. These include increases in the frequency of occurrence of glissades and overlapping saccades and reductions in the peak velocity and duration of saccades. In their study, fatigue was induced by the same step tracking task that was used to evaluate the changes in saccadic parameters. However, there is evidence that subjects experience extreme feelings of fatigue while performing such a task and that somehow the task is unnatural. The present study was designed to assess whether there are any differences in the various saccadic parameters obtained while subjects perform a step tracking task and a cognitive task involving the comparison of number strings. Both tasks were presented on a VDU screen. The second objective was to establish whether there are any changes in the parameters for either task as a result of prolonged performance. The results showed no major differences in the saccadic eye movements between the two tasks and no consistent changes resulting from prolonged performance.

Saccadic eye movements evoked by microstimulation of the fastigial nucleus of macaque monkeys

1988 ◽  
Vol 60 (3) ◽  
pp. 1036-1052 ◽  
Author(s):  
H. Noda ◽  
S. Murakami ◽  
J. Yamada ◽  
J. Tamada ◽  
Y. Tamaki ◽  
...  
Keyword(s):  
Eye Movements ◽  
White Matter ◽  
Purkinje Cells ◽  
Saccadic Eye Movements ◽  
The Other ◽  
Fastigial Nucleus ◽  
Threshold Region ◽  
Other Hand ◽  
Low Threshold ◽  
Stimulation Of

1. Systematic exploration throughout the deep cerebellar nuclei and white matter disclosed that the region from which saccadic eye movements (saccades) were evoked with weak currents (less than 10 microA) was confined to the fastigial nucleus and the adjacent white matter. 2. When an electrode for stimulation was advanced in the cerebellum, saccades were evoked in the direction of the stimulated side (ipsilateral saccades) as it entered the low-threshold region. In some tracks, particularly when the electrode was advanced in the medial portion of the fastigial nucleus, the direction of the evoked saccades changed from the ipsilateral to the contralateral. 3. The mappings with microstimulation disclosed that the ipsilateral saccades were elicited from a relatively wide region that included almost the full extent of the fastigial nucleus. The low-threshold region continued in the white matter caudally into vermal lobule VII and rostrally into the dorsal aspect of the brachium conjunctivum. On the other hand, the contralateral saccades were evoked from a relatively circumscribed region in the ventromedial portion of the fastigial nucleus. 4. The reversal in the direction of the horizontal component occurred always in a narrow zone in the core of the fastigial nucleus. The caudal part of this zone coincided with an ellipsoidal region where anterogradely labeled axons of the Purkinje cells terminated when HRP was injected into vermal lobule VII. 5. When bicuculline (0.2-1 microgram) was injected in the ellipsoidal region, the ipsilateral saccades evoked from the dorsocaudal aspect of the region were suppressed for several hours. On the other hand, the contralateral saccades evoked from the ventromedial portion of the fastigial nucleus were either unchanged or enhanced. 6. Because the ipsilateral saccades were suppressed by bicuculline, they were most probably evoked by stimulation of the presynaptic component of gamma-amino-butyric acid-(GABA) mediated synapses, namely the axons of Purkinje cells. 7. Because stimulation of the presynaptic component of the inhibitory synapses evoked ipsilateral saccades, activation of the postsynaptic component would evoke contralateral saccades. In fact, the distribution of the fastigial sites yielding contralateral saccades coincided with the course of axons of fastigial neurons arising in the ellipsoidal region. It is most likely, therefore, that the contralateral saccades were evoked by stimulation of fastigial neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

Effects of Phosphor Persistence on Perception and the Control of Eye Movements

Perception ◽  
1989 ◽  
Vol 18 (2) ◽  
pp. 257-264 ◽  
Author(s):  
Catherine Neary ◽  
Arnold J Wilkins
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
The Other ◽  
Saccadic Suppression ◽  
Rapid Eye Movement ◽  
Physiological Basis ◽  
Cathode Ray Tube ◽  
Ghost Image ◽  
Corrective Saccades

When a rapid eye movement (saccade) is made across material displayed on cathode ray tube monitors with short-persistence phosphors, various perceptual phenomena occur. The phenomena do not occur when the monitor has a long-persistence phosphor. These phenomena were observed for certain spatial arrays, their possible physiological basis noted, and their effect on the control of eye movements examined. When the display consisted simply of two dots, and a saccade was made from one to the other, a transient ghost image was seen just beyond the destination target. When the display consisted of vertical lines, tilting and displacement of the lines occurred. The phenomena were more intrusive for the latter display and there was a significant increase in the number of corrective saccades. These results are interpreted in terms of the effects of fluctuating illumination (and hence phosphor persistence) on saccadic suppression.

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