Suppressing Eye Movements Research Articles

Differences in color fading and recovery under sustained fixation.

More than two centuries ago, Swiss philosopher I. P. V. Troxler announced in 1804 that fixated images fade away during normal vision. Since this declaration, the phenomenon now known as Troxler fading has become the subject of intensive research. Many researchers were eager to find out why we experience image fading and under what conditions image restoration happens. Here, we investigated the dynamics of color stimulus fading and recovery under sustained eye fixation. The objective of the experiments was to find out which colors fade and recover faster under isoluminant conditions. The stimuli were eight blurred color rings extending to 13° in size. Four unique colors (red, yellow, green, and blue) and four intermediate colors (magenta, cyan, yellow-green, and orange) were used. Stimuli were displayed on a computer monitor with a gray background and were isoluminant to the background. The presentation of the stimulus lasted 2min and subjects were required to look at the fixation point in the middle of the ring and suppress eye movements. The task for subjects was to report the moments of change in the stimulus visibility by four stages of stimulus completeness. We found that all investigated colors undergo fading and recovery cycles during 2min of observation. The data suggest that magenta and cyan colors have faster stimulus fading and undergo more recovery cycles, while longer wavelength colors slow down stimulus fading.

Saccadic inhibition during free viewing in macaque monkeys.

Through the process of saccadic inhibition, visual events briefly suppress eye movements including microsaccades. In humans, saccadic inhibition has been shown to occur in response to the presentation of parafoveal or peripheral visual distractors during fixation and target-directed saccades and to physical changes of behaviorally relevant visual objects. In monkeys performing tasks that controlled eye movements, saccadic inhibition of microsaccades and target-directed saccades has been shown. Using eye data from three previously published studies, we investigated how saccade rate changed while monkeys were presented with visual stimuli under conditions with loose or no viewing demands. In two conditions, animals passively sat while an LED lamp flashed or screen-wide images appeared in front of them. In the third condition, images were repeated semiperiodically while animals had to maintain their gaze within a wide rectangular area and detect oddballs. Despite animals not being required to maintain fixation or make saccades to particular targets, the onset of visual events led to a temporary reduction of saccade rate across all conditions. Interestingly, saccadic inhibition was found at image offsets as well. These results show that saccadic inhibition occurs in monkeys during free viewing.NEW & NOTEWORTHY We investigated the time courses of saccade rate following visual stimuli during three conditions of free viewing in macaque monkeys. Under all conditions, saccade rate decreased transiently after the onset of visual stimuli. These results suggest that saccadic inhibition occurs during free viewing.

Modulation of inhibitory communication coordinates looking and reaching.

Looking and reaching are controlled by different brain regions and arecoordinated during natural behaviour1. Understanding how flexible, natural behaviours such as coordinated looking and reaching are controlled depends on understanding how neurons in different regions of the brain communicate2. Neural coherence in a gamma-frequency (40-90 Hz) band has been implicated in excitatory multiregional communication3. Inhibitory control mechanisms are also required to flexibly control behaviour4, but little is known about how neurons in one region transiently suppress individual neurons in another to support behaviour. How neuronal firing in a sender region transiently suppresses firing in a receiver region remains poorly understood. Here we study inhibitory communication during a flexible, natural behaviour, termed gaze anchoring, in which saccades are transiently inhibited by coordinated reaches. During gaze anchoring, we found that neurons in the reach region of the posterior parietal cortex can inhibit neuronal firing in the parietal saccade region to suppress eye movements and improve reach accuracy. Suppression is transient, only present around the coordinated reach, and greatest when reach neurons fire spikes with respect to beta-frequency (15-25 Hz) activity, not gamma-frequency activity. Our work provides evidence in the activity of single neurons for a novel mechanism of inhibitory communication in which beta-frequency neural coherence transiently inhibits multiregional communication to flexibly coordinate natural behaviour.

Functional connectivity of the Precuneus reflects effectiveness of visual restitution training in chronic hemianopia

Visual field defects in chronic hemianopia can improve through visual restitution training, yet not all patients benefit equally from this long and exhaustive procedure. Here, we asked if resting-state functional connectivity prior to visual restitution could predict training success. In two training sessions of eight weeks each, 20 patients with chronic hemianopia performed a visual discrimination task by directing spatial selective attention towards stimuli presented in either hemifield, while suppressing eye movements. We examined two effects: a sensitivity change in the attended (trained) minus the unattended (control) hemifield (i.e., a training-specific improvement), and an overall improvement (i.e., a total change in sensitivity after both sessions). We then identified five visual resting-state networks and evaluated their functional connectivity in relation to both training effects. We found that the functional connectivity strength between the anterior Precuneus and the Occipital Pole Network was positively related to the attention modulated (i.e., training-specific) improvement. No such relationship was found for the overall improvement or for the other visual networks of interest. Our finding suggests that the anterior Precuneus plays a role in attention-modulated visual field improvements. The resting-state functional connectivity between the anterior Precuneus and the Occipital Pole Network may thus serve as an imaging-based biomarker that quantifies a patient's potential capacity to direct spatial attention. This may help to identify hemianopia patients that are most likely to benefit from visual restitution training.

Eyes-Closed Increases the Usability of Brain-Computer Interfaces Based on Auditory Event-Related Potentials.

Recent research has demonstrated how brain-computer interfaces (BCI) based on auditory stimuli can be used for communication and rehabilitation. In these applications, users are commonly instructed to avoid eye movements while keeping their eyes open. This secondary task can lead to exhaustion and subjects may not succeed in suppressing eye movements. In this work, we investigate the option to use a BCI with eyes-closed. Twelve healthy subjects participated in a single electroencephalography (EEG) session where they were listening to a rapid stream of bisyllabic words while alternatively having their eyes open or closed. In addition, we assessed usability aspects for the two conditions with a questionnaire. Our analysis shows that eyes-closed does not reduce the number of eye artifacts and that event-related potential (ERP) responses and classification accuracies are comparable between both conditions. Importantly, we found that subjects expressed a significant general preference toward the eyes-closed condition and were also less tensed in that condition. Furthermore, switching between eyes-closed and eyes-open and vice versa is possible without a severe drop in classification accuracy. These findings suggest that eyes-closed should be considered as a viable alternative in auditory BCIs that might be especially useful for subjects with limited control over their eye movements.

The effects of constraining vision and eye movements on whole-body coordination during standing turns.

Turning the body towards a new direction is normally achieved via a top-down synergy whereby gaze (eye direction in space) leads the upper body segments, which in turn lead the feet. These anticipatory eye movements are observable even in darkness and constraining the initial eye movements modifies the stereotyped top-down reorientation sequence. Our aim was to elucidate the relative contributions of vision and eye movements to whole-body coordination during large standing turns by observing the effects of separately removing visual information or suppressing eye movements throughout the turn. We predicted that constraining eye movements would modify the steering synergy, whereas removing vision would have little effect. We found that preventing eye movements modified both timing and spatial characteristics of axial segment and feet rotation. When gaze was fixed, gait initiation, but not axial segment rotation, was delayed in comparison to both full vision and no vision turns. When eye movements were prevented, the predictable relationship between the extent head rotation led the body and peak head angular velocity was abolished suggesting that anticipatory head movements normally subserve gaze behaviour. In addition, stepping frequency significantly reduced during the gaze fixation condition but not during the no-vision condition, suggesting that oculomotor control is linked to stepping behaviour.

Inhibition of saccade and vergence eye movements in 3D space

Inhibitory capacity was investigated by measuring the eye movements of normal subjects asked to fixate a central point, and to suppress eye movements toward visual distracters appearing in the periphery or in depth. Eight right-handed young adults performed such a suppression or distracter task. In different conditions, the distracter could appear at 10 degrees left or right at a distance of 20, 40, or 150 cm (calling for horizontal saccades), or in a central position far or close (calling for convergence or divergence), or 7.5 degrees up or down at 40 or 150 cm (calling for vertical saccades). Eye movements were recorded binocularly with an infrared light eye-movement device. Results showed that (1) suppression performance was not perfect, as the subjects still produced eye movements; (2) errors were distributed unequally in three-dimensional space, with more frequent errors toward distracters calling for convergence, or leftward and downward saccades at a close distance; (3) distracters calling for saccade suppression yielded saccades in the direction of the distracter (that we called prosaccades), and saccades directed away from it (that we called spontaneous antisaccades); (4) for vergence, only distracters calling for convergence yielded errors, which were always promovements; (5) in addition, a small convergent drift was found for convergence distracters. Differences in the errors between saccade and vergence suggest that different inhibitory mechanisms may be involved in the two systems. Spatial left/right, up/down, and close/far asymmetries are interpreted in terms of attentional biases.

Horizontal saccades induced by stimulation of the central mesencephalic reticular formation.

The central mesencephalic reticular formation (cMRF) was electrically stimulated in the alert monkey. Saccadic eye movements were induced to the contralateral side in the horizontal plane at latencies of 18-35 ms. Smooth or slow eye deviations were not produced by cMRF stimulation. If the stimulus was given during slow phases of nystagmus, rapid eye movements were elicited, and the velocity of the slow phases was not affected. The function of cMRF neurons and/or of pathways that lie within it appear primarily related to generation of rapid eye movements in the horizontal plane. The amplitude of induced saccadic eye movements depended solely on the region of cMRF that was activated. When the stimulation frequency was lower, the latency was longer, but the size and characteristics of the induced movement were the same. The product of latency and stimulus frequency was approximately constant, suggesting that saccades had been triggered after a fixed number of pulses had been given. Stimulation of cMRF at frequencies that were too low to elicit rapid eye movements had a tonic effect on saccade generation. When the animal was having optokinetic nystagmus (OKN), stimulation modulated beat frequency according to the direction of the nystagmus: contralateral quick phases were facilitated and ipsilateral quick phases were suppressed. The frequencies of stimulation necessary to suppress ipsilateral quick phases increased as slow phase eye velocity increased. This demonstrates that both cMRF activity and slow phase velocity affect quick phase triggering. When the cMRF on both sides were simultaneously stimulated, the eyes were fixed in place, and no further rapid movements occurred until the stimulus had ended. Thus, activity in pathways and/or cells in cMRF is not only able to trigger saccades, but can also change the excitability of saccade generating mechanisms and promote fixation by suppressing eye movements. Two types of rapid eye movements were elicited from cMRF. From dorsal portions of cMRF saccades were induced whose size was relatively constant and not dependent on the initial position of the eyes in the orbit. The size of saccades increased from small to large as the stimulating electrode was advanced through cMRF from dorsal to ventral. This suggests that the tecto-bulbo-spinal efferents coursing through cMRF and/or cMRF neurons related to this input, are organized in a topographic fashion, with cells and fibers related to eye movements of increasing size being layered one beneath another.(ABSTRACT TRUNCATED AT 400 WORDS)

Evoked potentials to changes in the chromatic contrast and luminance contrast of checkboard stimulus patterns.

Many of the classical psychophysical studies of colour vision (and especially the experiments which established a foundation for the measurement of colour) were matching experiments (Maxwell, 1860; Abney, 1903; König, 1903). In these early studies the subject looked at a patch of light which was sharply divided down the middle (Wright, 1928, 1946; Guild, 1931). In some experiments his task was to adjust the brightnesses of the two halves of the stimulus until they appeared equal; in other experiments he adjusted the wavelengths of the two halves of the stimulus until he could just distinguish a difference between the hues of the left and right side of the stimulus. It has been well known to experimenters for at least 40 years that an over-enthusiastic subject could generate almost as many problems as a subject whose mind was not engaged with psychophysical considerations. McCree, working in W.D. Wright’s laboratory, carried out a study of this curious phenomenon (McCree, 1960). By voluntarily attempting to suppress eye movements by fixating as steadily as possible, many subjects were able to grossly degrade their power to distinguish between lights of different wavelengths. Both McCree and the present author turned out to be particularly susceptible to this effect of steady voluntary fixation. These two subjects were able to degrade very markedly their ability to distinguish between the hues of stimuli located as far apart as red and blue.KeywordsSpectral SensitivityRetinal ImageModulation DepthColour VisionCheckerboard PatternThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.