scholarly journals The role of action intentionality and effector in the subjective expansion of temporal duration after saccadic eye movements

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
David Melcher ◽  
Devpriya Kumar ◽  
Narayanan Srinivasan
Keyword(s):  
Eye Movements ◽  
Visual Processing ◽  
Saccadic Eye Movements ◽  
Intentional Binding ◽  
Opposite Pattern ◽  
Motor Action ◽  
Saccade Onset ◽  
Backward Shift ◽  
The Moment

Abstract Visual perception is based on periods of stable fixation separated by saccadic eye movements. Although naive perception seems stable (in space) and continuous (in time), laboratory studies have demonstrated that events presented around the time of saccades are misperceived spatially and temporally. Saccadic chronostasis, the “stopped clock illusion”, represents one such temporal distortion in which the movement of the clock hand after the saccade is perceived as lasting longer than usual. Multiple explanations for chronostasis have been proposed including action-backdating, temporal binding of the action towards the moment of its effect (“intentional binding”) and post-saccadic temporal dilation. The current study aimed to resolve this debate by using different types of action (keypress vs saccade) and varying the intentionality of the action. We measured both perceived onset of the motor action and perceived onset of an auditory tone presented at different delays after the keypress/saccade. The results showed intentional binding for the keypress action, with perceived motor onset shifted forwards in time and the time of the tone shifted backwards. Saccades resulted in the opposite pattern, showing temporal expansion rather than compression, especially with cued saccades. The temporal illusion was modulated by intentionality of the movement. Our findings suggest that saccadic chronostasis is not solely dependent on a backward shift in perceived saccade onset, but instead reflects a temporal dilation. This percept of an effectively “longer” period at the beginning of a new fixation may reflect the pattern of suppressed, and then enhanced, visual processing around the time of saccades.

scholarly journals The role of fixation disengagement in the parallel programming of sequences of saccades

2019 ◽  
Vol 237 (11) ◽  
pp. 3033-3045
Author(s):  
Eugene McSorley ◽  
Iain D. Gilchrist ◽  
Rachel McCloy
Keyword(s):  
Eye Movements ◽  
Parallel Programming ◽  
Response Times ◽  
Saccadic Eye Movements ◽  
Gap Effect ◽  
Task Completion ◽  
Published Data ◽  
Trial Duration ◽  
Visual Tasks

Abstract One of the core mechanisms involved in the control of saccade responses to selected target stimuli is the disengagement from the current fixation location, so that the next saccade can be executed. To carry out everyday visual tasks, we make multiple eye movements that can be programmed in parallel. However, the role of disengagement in the parallel programming of saccades has not been examined. It is well established that the need for disengagement slows down saccadic response time. This may be important in allowing the system to program accurate eye movements and have a role to play in the control of multiple eye movements but as yet this remains untested. Here, we report two experiments that seek to examine whether fixation disengagement reduces saccade latencies when the task completion demands multiple saccade responses. A saccade contingent paradigm was employed and participants were asked to execute saccadic eye movements to a series of seven targets while manipulating when these targets were shown. This both promotes fixation disengagement and controls the extent that parallel programming can occur. We found that trial duration decreased as more targets were made available prior to fixation: this was a result both of a reduction in the number of saccades being executed and in their saccade latencies. This supports the view that even when fixation disengagement is not required, parallel programming of multiple sequential saccadic eye movements is still present. By comparison with previous published data, we demonstrate a substantial speeded of response times in these condition (“a gap effect”) and that parallel programming is attenuated in these conditions.

Role of Saccadic Eye Movements in Cognitive Processes

2009 ◽  
Vol 147 (1) ◽  
pp. 11-14
Author(s):  
N. A. Ryabchikova ◽  
B. H. Bazyian ◽  
V. B. Poliansky ◽  
O. A. Pletnev
Keyword(s):  
Eye Movements ◽  
Cognitive Processes ◽  
Saccadic Eye Movements

5. Role of the amygdala in the control of saccadic eye movements

2008 ◽  
Vol 119 (9) ◽  
pp. e166
Author(s):  
S.L. Gonzalez Andino ◽  
C. Laine ◽  
R. Grave de Peralta ◽  
K.L. Gothard
Keyword(s):  
Eye Movements ◽  
Saccadic Eye Movements

scholarly journals Contrast sensitivity, V1 neural activity, and natural vision

2017 ◽  
Vol 117 (2) ◽  
pp. 492-508 ◽  
Author(s):  
James E. Niemeyer ◽  
Michael A. Paradiso
Keyword(s):  
Eye Movements ◽  
Contrast Sensitivity ◽  
Visual Processing ◽  
Brain Area ◽  
Saccadic Eye Movements ◽  
Visual Sensitivity ◽  
Natural Image ◽  
Spatial Frequencies ◽  
Natural Vision ◽  
Common Laboratory

Contrast sensitivity is fundamental to natural visual processing and an important tool for characterizing both visual function and clinical disorders. We simultaneously measured contrast sensitivity and neural contrast response functions and compared measurements in common laboratory conditions with naturalistic conditions. In typical experiments, a subject holds fixation and a stimulus is flashed on, whereas in natural vision, saccades bring stimuli into view. Motivated by our previous V1 findings, we tested the hypothesis that perceptual contrast sensitivity is lower in natural vision and that this effect is associated with corresponding changes in V1 activity. We found that contrast sensitivity and V1 activity are correlated and that the relationship is similar in laboratory and naturalistic paradigms. However, in the more natural situation, contrast sensitivity is reduced up to 25% compared with that in a standard fixation paradigm, particularly at lower spatial frequencies, and this effect correlates with significant reductions in V1 responses. Our data suggest that these reductions in natural vision result from fast adaptation on one fixation that lowers the response on a subsequent fixation. This is the first demonstration of rapid, natural-image adaptation that carries across saccades, a process that appears to constantly influence visual sensitivity in natural vision. NEW & NOTEWORTHY Visual sensitivity and activity in brain area V1 were studied in a paradigm that included saccadic eye movements and natural visual input. V1 responses and contrast sensitivity were significantly reduced compared with results in common laboratory paradigms. The parallel neural and perceptual effects of eye movements and stimulus complexity appear to be due to a form of rapid adaptation that carries across saccades.

Role of cat pontine burst neurons in generation of saccadic eye movements.

1981 ◽  
Vol 46 (3) ◽  
pp. 387-408 ◽  
Author(s):  
C R Kaneko ◽  
C Evinger ◽  
A F Fuchs
Keyword(s):  
Eye Movements ◽  
Saccadic Eye Movements ◽  
Burst Neurons

Use of interrupted saccade paradigm to study spatial and temporal dynamics of saccadic burst cells in superior colliculus in monkey

1994 ◽  
Vol 72 (6) ◽  
pp. 2754-2770 ◽  
Author(s):  
E. L. Keller ◽  
J. A. Edelman
Keyword(s):  
Eye Movements ◽  
Superior Colliculus ◽  
Temporal Dynamics ◽  
Saccadic Eye Movements ◽  
Eye Position ◽  
Visual Response ◽  
Intermediate Layers ◽  
Saccade Onset ◽  
Spatial And Temporal Dynamics ◽  
Motor Error

1. We recorded the spatial and temporal dynamics of saccade-related burst neurons (SRBNs) found in the intermediate layers of the superior colliculus (SC) in the alert, behaving monkey. These burst cells are normally the first neurons recorded during radially directed microelectrode penetrations of the SC after the electrode has left the more dorsally situated visual layers. They have spatially delimited movement fields whose centers describe the well-studied motor map of the SC. They have a rather sharp, saccade-locked burst of activity that peaks just before saccade onset and then declines steeply during the saccade. Many of these cells, when recorded during saccade trials, also have an early, transient visual response and an irregular prelude of presaccadic activity. 2. Because saccadic eye movements normally have very stereotyped durations and velocity trajectories that vary systematically with saccade size, it has been difficult in the past to establish quantitatively whether the activity of SRBNs temporally codes dynamic saccadic control signals, e.g., dynamic motor error or eye velocity, where dynamic motor error is defined as a signal proportional to the instantaneous difference between desired final eye position and the actual eye position during a saccade. It has also not been unequivocally established whether SRBNs participate in an organized spatial shift of ensemble activity in the intermediate layers of the SC during saccadic eye movements. 3. To address these issues, we studied the activity of SRBNs using an interrupted saccade paradigm. Saccades were interrupted with pulsatile electrical stimulation through a microelectrode implanted in the omnipauser region of the brain stem while recordings were made simultaneously from single SRBNs in the SC. 4. Shortly after the beginning of the stimulation (which was electronically triggered at saccade onset), the eyes decelerated rapidly and stopped completely. When the high-frequency (typically 300-400 pulses per second) stimulation was terminated (average duration 12 ms), the eye movement was reinitiated and a resumed saccade was made accurately to the location of the target. 5. When we recorded from SRBNs in the more caudal colliculus, which were active for large saccades, cell discharge was powerfully and rapidly suppressed by the stimulation (average latency = 3.8 ms). Activity in the same cells started again just before the onset of the resumed saccade and continued during this saccade even though it has a much smaller amplitude than would normally be associated with significant discharge for caudal SC cells.(ABSTRACT TRUNCATED AT 400 WORDS)

Role of vestibular adaptation in vestibular rehabilitation

1998 ◽  
Vol 119 (1) ◽  
pp. 49-54 ◽  
Author(s):  
Susan J. Herdman
Keyword(s):  
Eye Movements ◽  
Postural Stability ◽  
Saccadic Eye Movements ◽  
Human Beings ◽  
Compensatory Mechanisms ◽  
Ocular Reflex ◽  
Reflex Modification ◽  
Postural Responses ◽  
Vestibular Cues

Recovery of gaze and postural stability in human beings with vestibular deficits is well documented. The mechanisms that contribute to this recovery form the basis for the exercises used in the rehabilitation of these patients. These mechanisms include the central preprogramming of eye movements and of postural responses, the potentiation of the cervico-ocular reflex, modification of saccadic eye movements, and the substitution of visual and somatosensory cues for the lost vestibular cues. The mechanism most successful in contributing to recovery, however, is probably adaptation of the vestibular system itself. Understanding the various compensatory mechanisms and their limitations for improving gaze and postural stability should lead to more effective treatment of these patients. (Otolaryngol Head Neck Surg 1998;119:49–54.)

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