The effect of expectations on slow oculomotor control—IV. Anticipatory smooth eye movements depend on prior target motions

1984 ◽  
Vol 24 (3) ◽  
pp. 197-210 ◽  
Author(s):  
Eileen Kowler ◽  
Albert J. Martins ◽  
M. Pavel
Keyword(s):  
Eye Movements ◽  
Oculomotor Control ◽  
Anticipatory Smooth Eye Movements

scholarly journals Neural Basis of Visually Guided Head Movements Studied With fMRI

2003 ◽  
Vol 89 (5) ◽  
pp. 2516-2527 ◽  
Author(s):  
Laurent Petit ◽  
Michael S. Beauchamp
Keyword(s):  
Eye Movements ◽  
Head Movement ◽  
Brain Activity ◽  
Posterior Part ◽  
Vestibular Stimulation ◽  
Head Movements ◽  
Oculomotor Control ◽  
Imaging Studies ◽  
Neural Basis ◽  
Temporoparietal Junction

We used event-related fMRI to measure brain activity while subjects performed saccadic eye, head, and gaze movements to visually presented targets. Two distinct patterns of response were observed. One set of areas was equally active during eye, head, and gaze movements and consisted of the superior and inferior subdivisions of the frontal eye fields, the supplementary eye field, the intraparietal sulcus, the precuneus, area MT in the lateral occipital sulcus and subcortically in basal ganglia, thalamus, and the superior colliculus. These areas have been previously observed in functional imaging studies of human eye movements, suggesting that a common set of brain areas subserves both oculomotor and head movement control in humans, consistent with data from single-unit recording and microstimulation studies in nonhuman primates that have described overlapping eye- and head-movement representations in oculomotor control areas. A second set of areas was active during head and gaze movements but not during eye movements. This set of areas included the posterior part of the planum temporale and the cortex at the temporoparietal junction, known as the parieto-insular vestibular cortex (PIVC). Activity in PIVC has been observed during imaging studies of invasive vestibular stimulation, and we confirm its role in processing the vestibular cues accompanying natural head movements. Our findings demonstrate that fMRI can be used to study the neural basis of head movements and show that areas that control eye movements also control head movements. In addition, we provide the first evidence for brain activity associated with vestibular input produced by natural head movements as opposed to invasive caloric or galvanic vestibular stimulation.

Abstract W P140: Post-stroke Oculomotor Abnormalities evident during Objective Eye Tracking but Not under Clinical Assessment

Stroke ◽  
2015 ◽  
Vol 46 (suppl_1) ◽  
Author(s):  
John-Ross Rizzo ◽  
Todd Hudson ◽  
Briana Kowal ◽  
Michal Wiseman ◽  
Preeti Raghavan
Keyword(s):  
Motor Control ◽  
Eye Movements ◽  
Eye Movement ◽  
Oculomotor Control ◽  
Healthy Controls ◽  
Visually Guided ◽  
Stroke Patients ◽  
Movement Execution ◽  
Post Stroke ◽  
Control Post

Introduction: Visual abnormalities and manual motor control have been studied extensively after stroke, but an understanding of oculomotor control post-stroke has not. Recent studies have revealed that in visually guided reaches arm movements are planned during eye movement execution, which may contribute to increased task complexity. In fact, in healthy controls during visually guided reaches, the onset of eye movement is delayed, its velocity reduced, and endpoint errors are larger relative to isolated eye movements. Our objective in this experiment was to examine the temporal properties of eye movement execution for stroke patients with no diagnosed visual impairment. The goal is to improve understanding of oculomotor control in stroke relative to normal function, and ultimately further understand its coordination with manual motor control during joint eye and hand movements. We hypothesized that stroke patients would show abnormal initiation or onset latency for saccades made in an eye movement task, as compared to healthy controls. Methods: We measured the kinematics of eye movements during point-to-point saccades; there was an initial static, fixation point and the stimulus was a flashed target on a computer monitor. We used a video-based eye tracker for objective recording of the eye at a sampling frequency of 2000 Hz (SR Research, Eyelink). 10 stroke subjects, over 4 months from injury and with no diagnosed visual impairment, and 10 healthy controls completed 432 saccades in a serial fashion. Results: Stroke patients had significantly faster onset latencies as compared to healthy controls during saccades (99.5ms vs. 245.2ms, p=0.00058). Conclusion: A better understanding of the variations in oculomotor control post-stroke, which may go unnoticed during clinical assessment, may improve understanding of how eye control synchronizes with arm or manual motor control. This knowledge could assist in tailoring rehabilitative strategies to amplify motor recovery. For next steps, we will perform objective eye and hand recordings during visually guided reaches post-stroke to better understand the harmonization or lack thereof after neurologic insult.

scholarly journals Unrestricted eye movements strengthen causal connectivity from hippocampal to oculomotor regions during scene construction

2021 ◽  
Author(s):  
Natalia Ladyka-Wojcik ◽  
Zhong-Xu Liu ◽  
Jennifer D. Ryan
Keyword(s):  
Eye Movements ◽  
Visual Processing ◽  
Oculomotor System ◽  
Visual Input ◽  
Causal Modeling ◽  
Oculomotor Control ◽  
Visual Stream ◽  
Functional Connections ◽  
Free Viewing ◽  
Scene Construction

Scene construction is a key component of memory recall, navigation, and future imagining, and relies on the medial temporal lobes (MTL). A parallel body of work suggests that eye movements may enable the imagination and construction of scenes, even in the absence of external visual input. There are vast structural and functional connections between regions of the MTL and those of the oculomotor system. However, the directionality of connections between the MTL and oculomotor control regions, and how it relates to scene construction, has not been studied directly in human neuroimaging. In the current study, we used dynamic causal modeling (DCM) to investigate this relationship at a mechanistic level using a scene construction task in which participants' eye movements were either restricted (fixed-viewing) or unrestricted (free-viewing). By omitting external visual input, and by contrasting free- versus fixed- viewing, the directionality of neural connectivity during scene construction could be determined. As opposed to when eye movements were restricted, allowing free viewing during construction of scenes strengthened top-down connections from the MTL to the frontal eye fields, and to lower-level cortical visual processing regions, suppressed bottom-up connections along the visual stream, and enhanced vividness of the constructed scenes. Taken together, these findings provide novel, non-invasive evidence for the causal architecture between the MTL memory system and oculomotor system associated with constructing vivid mental representations of scenes.

scholarly journals Neural correlates of subsequent memory-related gaze reinstatement

2021 ◽  
Author(s):  
Jordana S. Wynn ◽  
Zhong-Xu Liu ◽  
Jennifer D. Ryan
Keyword(s):  
Eye Movements ◽  
Basal Ganglia ◽  
Recognition Memory ◽  
Visual Processing ◽  
Memory Task ◽  
Neural Correlates ◽  
Oculomotor Control ◽  
Related Activity ◽  
Pattern Similarity ◽  
Occipital Pole

AbstractMounting evidence linking gaze reinstatement- the recapitulation of encoding-related gaze patterns during retrieval- to behavioral measures of memory suggests that eye movements play an important role in mnemonic processing. Yet, the nature of the gaze scanpath, including its informational content and neural correlates, has remained in question. In the present study, we examined eye movement and neural data from a recognition memory task to further elucidate the behavioral and neural bases of functional gaze reinstatement. Consistent with previous work, gaze reinstatement during retrieval of freely-viewed scene images was greater than chance and predictive of recognition memory performance. Gaze reinstatement was also associated with viewing of informationally salient image regions at encoding, suggesting that scanpaths may encode and contain high-level scene content. At the brain level, gaze reinstatement was predicted by encoding-related activity in the occipital pole and basal ganglia, neural regions associated with visual processing and oculomotor control. Finally, cross-voxel brain pattern similarity analysis revealed overlapping subsequent memory and subsequent gaze reinstatement modulation effects in the parahippocampal place area and hippocampus, in addition to the occipital pole and basal ganglia. Together, these findings suggest that encoding-related activity in brain regions associated with scene processing, oculomotor control, and memory supports the formation, and subsequent recapitulation, of functional scanpaths. More broadly, these findings lend support to Scanpath Theory’s assertion that eye movements both encode, and are themselves embedded in, mnemonic representations.

scholarly journals Anticipatory smooth eye movements adapt to higher-order probabilistic structure of the environment

2021 ◽  
Vol 21 (9) ◽  
pp. 2003
Author(s):  
Vanessa Carneiro Morita ◽  
Guillaume S Masson ◽  
Anna Montagnini
Keyword(s):  
Eye Movements ◽  
Higher Order ◽  
Probabilistic Structure ◽  
Anticipatory Smooth Eye Movements

scholarly journals Electrical microstimulation evokes saccades in posterior parietal cortex of common marmosets

2019 ◽  
Vol 122 (4) ◽  
pp. 1765-1776 ◽  
Author(s):  
Maryam Ghahremani ◽  
Kevin D. Johnston ◽  
Liya Ma ◽  
Lauren K. Hayrynen ◽  
Stefan Everling
Keyword(s):  
Eye Movements ◽  
Parietal Cortex ◽  
Posterior Parietal Cortex ◽  
Common Marmoset ◽  
Primate Species ◽  
Oculomotor Control ◽  
Electrical Microstimulation ◽  
Cortical Areas ◽  
Posterior Parietal ◽  
The Common

The common marmoset ( Callithrix jacchus) is a small-bodied New World primate increasing in prominence as a model animal for neuroscience research. The lissencephalic cortex of this primate species provides substantial advantages for the application of electrophysiological techniques such as high-density and laminar recordings, which have the capacity to advance our understanding of local and laminar cortical circuits and their roles in cognitive and motor functions. This is particularly the case with respect to the oculomotor system, as critical cortical areas of this network such as the frontal eye fields (FEF) and lateral intraparietal area (LIP) lie deep within sulci in macaques. Studies of cytoarchitecture and connectivity have established putative homologies between cortical oculomotor fields in marmoset and macaque, but physiological investigations of these areas, particularly in awake marmosets, have yet to be carried out. Here we addressed this gap by probing the function of posterior parietal cortex of the common marmoset with electrical microstimulation. We implanted two animals with 32-channel Utah arrays at the location of the putative area LIP and applied microstimulation while they viewed a video display and made untrained eye movements. Similar to previous studies in macaques, stimulation evoked fixed-vector and goal-directed saccades, staircase saccades, and eyeblinks. These data demonstrate that area LIP of the marmoset plays a role in the regulation of eye movements, provide additional evidence that this area is homologous with that of the macaque, and further establish the marmoset as a valuable model for neurophysiological investigations of oculomotor and cognitive control. NEW & NOTEWORTHY The macaque monkey has been the preeminent model for investigations of oculomotor control, but studies of cortical areas are limited, as many of these areas are buried within sulci in this species. Here we applied electrical microstimulation to the putative area LIP of the lissencephalic cortex of awake marmosets. Similar to the macaque, microstimulation evoked contralateral saccades from this area, supporting the marmoset as a valuable model for studies of oculomotor control.

Quick phases control ocular torsion during smooth pursuit

2011 ◽  
Vol 106 (5) ◽  
pp. 2151-2166 ◽  
Author(s):  
Bernhard J. M. Hess ◽  
Jakob S. Thomassen
Keyword(s):  
Eye Movements ◽  
Visual Field ◽  
Rotation Axis ◽  
Three Dimensional ◽  
Oculomotor Control ◽  
Visually Guided ◽  
Open Questions ◽  
Spatial Frequencies ◽  
Eye Rotation ◽  
Smooth Tracking

One of the open questions in oculomotor control of visually guided eye movements is whether it is possible to smoothly track a target along a curvilinear path across the visual field without changing the torsional stance of the eye. We show in an experimental study of three-dimensional eye movements in subhuman primates ( Macaca mulatta) that although the pursuit system is able to smoothly change the orbital orientation of the eye's rotation axis, the smooth ocular motion was interrupted every few hundred milliseconds by a small quick phase with amplitude <1.5° while the animal tracked a target along a circle or ellipse. Specifically, during circular pursuit of targets moving at different angular eccentricities (5°, 10°, and 15°) relative to straight ahead at spatial frequencies of 0.067 and 0.1 Hz, the torsional amplitude of the intervening quick phases was typically around 1° or smaller and changed direction for clockwise vs. counterclockwise tracking. Reverse computations of the eye rotation based on the recorded angular eye velocity showed that the quick phases facilitate the overall control of ocular orientation in the roll plane, thereby minimizing torsional disturbances of the visual field. On the basis of a detailed kinematic analysis, we suggest that quick phases during curvilinear smooth tracking serve to minimize deviations from Donders' law, which are inevitable due to the spherical configuration space of smooth eye movements.

Neuronal responses in rabbit cingulate cortex linked to quick-phase eye movements during nystagmus

1988 ◽  
Vol 59 (3) ◽  
pp. 922-936 ◽  
Author(s):  
R. W. Sikes ◽  
B. A. Vogt ◽  
H. A. Swadlow
Keyword(s):  
Eye Movements ◽  
Visual Information ◽  
Light Emitting Diode ◽  
Cingulate Cortex ◽  
Vestibular Stimulation ◽  
Oculomotor Control ◽  
Infrared Light ◽  
Thalamic Nuclei ◽  
Light Emitting ◽  
Layer V

1. Responses of single units in area 29 of cingulate cortex were examined in alert rabbits during vestibular and optokinetic nystagmus. Eye movements were measured by optically detecting the position of an infrared light-emitting diode attached to the cornea. 2. Fourteen percent of cingulate cells (68 of 477 isolated units) had responses that were correlated to the occurrence of quick phases. Latencies ranged from 60 ms before to 220 ms after the onset of the quick phase with a mean of 70 ms and standard deviation of 58 ms. Most units responded during or following quick phases, although four units had responses that preceded the quick-phase onset. 3. Unitary responses during quick phases were not due to visual field movement, since these responses occurred in the dark as well as the light. The responses were not dependent upon vestibular stimulation, since responses related to spontaneous saccadelike eye movements were observed in cingulate quick-phase neurons. 4. The majority (37 of 52) of the quick-phase neurons had a directional preference. Approximately equal numbers of directional units responded to quick phases directed ipsilaterally and contralaterally with respect to the recording site. 5. About one-fourth of the quick-phase units were bidirectional (15 of 52) with virtually equal responses to ipsilaterally and contralaterally directed quick phases. 6. Auditory and/or somatosensory responses were observed in only five of the quick-phase cells. All such multimodal units were bidirectional. 7. The quick-phase units were histologically confirmed to be primarily in area 29d of cingulate cortex. Although most cells were located in layer V, some were isolated in layer II-III. 8. Cingulate cortex has reciprocal connections with visual cortex and oculomotor-related thalamic nuclei and projects to the layers of the superior colliculus that are involved in oculomotor control. Responses to quick phases in cingulate neurons may synchronize cingulate cortex responsiveness with the arrival of new, and potentially significant, visual information.

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