scholarly journals Eye position modulation of visual responses in the lateral intraparietal area lags the eye movement

2010 ◽  
Vol 4 ◽  
Author(s):  
Goldberg Michael
Keyword(s):  
Eye Movement ◽  
Eye Position ◽  
Visual Responses ◽  
Lateral Intraparietal Area

Properties of superior vestibular nucleus neurons projecting to the cerebellar flocculus in the squirrel monkey

1993 ◽  
Vol 69 (2) ◽  
pp. 642-645 ◽  
Author(s):  
Y. Zhang ◽  
A. M. Partsalis ◽  
S. M. Highstein
Keyword(s):  
Eye Movement ◽  
Squirrel Monkey ◽  
Vestibular Nucleus ◽  
Squirrel Monkeys ◽  
Eye Position ◽  
Oculomotor Nucleus ◽  
Position Sensitivity ◽  
Cerebellar Flocculus ◽  
The Mean ◽  
Superior Vestibular Nucleus

1. Properties of superior vestibular nucleus (SVN) neurons and their projection to the cerebellar flocculus were studied in alert squirrel monkeys by using chronic unit and eye movement recording and microstimulation techniques. Twenty-three cells were antidromically activated from the ipsilateral flocculus, and seventeen of these were also orthodromically activated from the ipsilateral VIIth nerve at monosynaptic latencies. Only 1 of these 23 units was also inhibited by flocculus stimulation. According to their response properties, 9 of the cells were pure vestibular, 2 were vestibular-pause, and 12 were position-vestibular cells. The mean eye position sensitivity of these position-vestibular cells was significantly lower than that of cells projecting to the oculomotor nucleus (OMN). No eye movement-only neurons were antidromically activated from the flocculus. No cells could be antidromically activated from both the oculomotor nucleus and the flocculus.

Discharge patterns in nucleus prepositus hypoglossi and adjacent medial vestibular nucleus during horizontal eye movement in behaving macaques

1992 ◽  
Vol 68 (1) ◽  
pp. 319-332 ◽  
Author(s):  
J. L. McFarland ◽  
A. F. Fuchs
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
Smooth Pursuit ◽  
Vestibular Nucleus ◽  
Medial Vestibular Nucleus ◽  
Eye Position ◽  
Head Velocity ◽  
Firing Rates ◽  
Prepositus Hypoglossi ◽  
Eye Velocity

1. Monkeys were trained to perform a variety of horizontal eye tracking tasks designed to reveal possible eye movement and vestibular sensitivities of neurons in the medulla. To test eye movement sensitivity, we required stationary monkeys to track a small spot that moved horizontally. To test vestibular sensitivity, we rotated the monkeys about a vertical axis and required them to fixate a target rotating with them to suppress the vestibuloocular reflex (VOR). 2. All of the 100 units described in our study were recorded from regions of the medulla that were prominently labeled after injections of horseradish peroxidase into the abducens nucleus. These regions include the nucleus prepositus hypoglossi (NPH), the medial vestibular nucleus (MVN), and their common border (the “marginal zone”). We report here the activities of three different types of neurons recorded in these regions. 3. Two types responded only during eye movements per se. Their firing rates increased with eye position; 86% had ipsilateral “on” directions. Almost three quarters (73%) of these medullary neurons exhibited a burst-tonic discharge pattern that is qualitatively similar to that of abducens motoneurons. There were, however, quantitative differences in that these medullary burst-position neurons were less sensitive to eye position than were abducens motoneurons and often did not pause completely for saccades in the off direction. The burst of medullary burst position neurons preceded the saccade by an average of 7.6 +/- 1.7 (SD) ms and, on average, lasted the duration of the saccade. The number of spikes in the burst was well correlated with saccade size. The second type of eye movement neuron displayed either no discernible burst or an inconsistent one for on-direction saccades and will be referred to as medullary position neurons. Neither the burst-position nor the position neurons responded when the animals suppressed the VOR; hence, they displayed no vestibular sensitivity. 4. The third type of neuron was sensitive to both eye movement and vestibular stimulation. These neurons increased their firing rates during horizontal head rotation and smooth pursuit eye movements in the same direction; most (76%) preferred ipsilateral head and eye movements. Their firing rates were approximately in phase with eye velocity during sinusoidal smooth pursuit and with head velocity during VOR suppression; on average, their eye velocity sensitivity was 50% greater than their vestibular sensitivity. Sixty percent of these eye/head velocity cells were also sensitive to eye position. 5. The NPH/MVN region contains many neurons that could provide an eye position signal to abducens neurons.(ABSTRACT TRUNCATED AT 400 WORDS)

Optokinetic Eye Movements Elicited by Radial Optic Flow in the Macaque Monkey

1998 ◽  
Vol 79 (3) ◽  
pp. 1461-1480 ◽  
Author(s):  
Markus Lappe ◽  
Martin Pekel ◽  
Klaus-Peter Hoffmann
Keyword(s):  
Eye Movements ◽  
Flow Field ◽  
Eye Movement ◽  
Optic Flow ◽  
Macaque Monkey ◽  
Flow Fields ◽  
Movement Direction ◽  
Slow Phase ◽  
Eye Position ◽  
Self Motion

Lappe, Markus, Martin Pekel, and Klaus-Peter Hoffmann. Optokinetic eye movements elicited by radial optic flow in the macaque monkey. J. Neurophysiol. 79: 1461–1480, 1998. We recorded spontaneous eye movements elicited by radial optic flow in three macaque monkeys using the scleral search coil technique. Computer-generated stimuli simulated forward or backward motion of the monkey with respect to a number of small illuminated dots arranged on a virtual ground plane. We wanted to see whether optokinetic eye movements are induced by radial optic flow stimuli that simulate self-movement, quantify their parameters, and consider their effects on the processing of optic flow. A regular pattern of interchanging fast and slow eye movements with a frequency of 2 Hz was observed. When we shifted the horizontal position of the focus of expansion (FOE) during simulated forward motion (expansional optic flow), median horizontal eye position also shifted in the same direction but only by a smaller amount; for simulated backward motion (contractional optic flow), median eye position shifted in the opposite direction. We relate this to a change in Schlagfeld typically observed in optokinetic nystagmus. Direction and speed of slow phase eye movements were compared with the local flow field motion in gaze direction (the foveal flow). Eye movement direction matched well the foveal motion. Small systematic deviations could be attributed to an integration of the global motion pattern. Eye speed on average did not match foveal stimulus speed, as the median gain was only ∼0.5–0.6. The gain was always lower for expanding than for contracting stimuli. We analyzed the time course of the eye movement immediately after each saccade. We found remarkable differences in the initial development of gain and directional following for expansion and contraction. For expansion, directional following and gain were initially poor and strongly influenced by the ongoing eye movement before the saccade. This was not the case for contraction. These differences also can be linked to properties of the optokinetic system. We conclude that optokinetic eye movements can be elicited by radial optic flow fields simulating self-motion. These eye movements are linked to the parafoveal flow field, i.e., the motion in the direction of gaze. In the retinal projection of the optic flow, such eye movements superimpose retinal slip. This results in complex retinal motion patterns, especially because the gain of the eye movement is small and variable. This observation has special relevance for mechanisms that determine self-motion from retinal flow fields. It is necessary to consider the influence of eye movements in optic flow analysis, but our results suggest that direction and speed of an eye movement should be treated differently.

Discharge characteristics of medial rectus and abducens motoneurons in the goldfish

1991 ◽  
Vol 66 (6) ◽  
pp. 2125-2140 ◽  
Author(s):  
A. M. Pastor ◽  
B. Torres ◽  
J. M. Delgado-Garcia ◽  
R. Baker
Keyword(s):  
Eye Movements ◽  
Firing Rate ◽  
Eye Movement ◽  
Vestibular Stimulation ◽  
Medial Rectus ◽  
Eye Position ◽  
Sensory Stimuli ◽  
Time Constants ◽  
Recruitment Threshold ◽  
Eye Blink

1. The discharge of antidromically identified medial rectus and abducens motoneurons was recorded in restrained unanesthesized goldfish during spontaneous eye movements and in response to vestibular and optokinetic stimulation. 2. All medial rectus and abducens motoneurons exhibited a similar discharge pattern. A burst of spikes accompanied spontaneous saccades and fast phases during vestibular and optokinetic nystagmus in the ON-direction. Firing rate decreased for the same eye movements in the OFF-direction. All units showed a steady firing rate proportional to eye position beyond their recruitment threshold. 3. Motoneuronal position (ks) and velocity (rs) sensitivity for spontaneous eye movements were calculated from the slope of the rate-position and rate-velocity linear regression lines, respectively. The averaged ks and rs values of medial rectus motoneurons were higher than those of abducens motoneurons. The differences in motoneuronal sensitivity coupled with structural variations in the lateral versus the medial rectus muscle suggest that symmetric nasal and temporal eye movements are preserved by different motor unit composition. Although the abducens nucleus consists of distinct rostral and caudal subgroups, mean ks and rs values were not significantly different between the two populations. 4. Every abducens and medial rectus motoneuron fired an intense burst of spikes during its corresponding temporal or nasal activation phase of the "eye blink." This eye movement consisted of a sequential, rather than a synergic, contraction of both vertical and horizontal extraocular muscles. The eye blink could act neither as a protective reflex nor as a goal-directed eye movement because it could not be evoked in response to sensory stimuli. We propose a role for the blink in recentering eye position. 5. Motoneuronal firing rate after ON-directed saccades decreased exponentially before reaching the sustained discharge proportional to the new eye position. Time constants of the exponential decay ranged from 50 to 300 ms. Longer time constants after the saccade were associated with backward drifts of eye position and shorter time constants with onward drifts. These postsaccadic slide signals are suggested to encode the transition of eye position to the new steady level. 6. Motoneurons modulated sinusoidally in response to sinusoidal head rotation in the dark, but for a part of the cycle they went into cutoff, dependent on their eye position recruitment threshold. Eye position (kv) and velocity (rv) sensitivity during vestibular stimulation were measured at frequencies between 1/16 and 2 Hz. Motoneuronal time constants (tau v = rv/kv) decreased on the average by 25% with the frequency of vestibular stimulation.(ABSTRACT TRUNCATED AT 400 WORDS)

Visuomotor functions of central thalamus in monkey. II. Unit activity related to visual events, targeting, and fixation

1984 ◽  
Vol 51 (6) ◽  
pp. 1175-1195 ◽  
Author(s):  
J. Schlag ◽  
M. Schlag-Rey
Keyword(s):  
Eye Movement ◽  
Receptive Fields ◽  
Stimulus Onset ◽  
Visual Responses ◽  
Visual Events ◽  
Response Enhancement ◽  
Dim Light ◽  
Central Thalamus ◽  
Thalamic Region ◽  
Sustained Responses

In alert monkeys, single-unit responses to visual stimuli were recorded in the central thalamic region where eye movement-related activity has been observed (33). Usually, the stimuli were 1 degree annulus patterns of dim light presented at unpredictable locations on a tangent screen. The animals were trained on two tasks: one in which they delivered the stimulus themselves by pressing a panel that they had to release immediately when the stimulus shape changed to a square, and another one in which the stimulus was turned on by the experimenter and the monkeys were rewarded for fixating this target for a predetermined length of time. In both tasks, continuous stimulus fixation was required. Receptive fields were tested with and without a fixation point. Retinal coordinates of stimuli were obtained by subtracting eye-position coordinates from stimulus coordinates in space, the monkey's head being fixed. Unit responses in the cases where targeting occurred or did not occur were analyzed separately. Transient responses were observed in 63 units and sustained responses in 44 units. Among the 63 units responding transiently, 42 did so irrespective of targeting. Their receptive fields were very large, generally including the fovea, and predominantly contralateral when the fields were asymmetric. The responses of the other 21 units depended on the occurrence of targeting. They were called visually triggered eye movement-related responses (VTEM). VTEM units were further subdivided in 9 units active only with targeting and 12 units showing the classical phenomenon of "response enhancement" under this condition. VTEM units were contrasted to six units that were both passively visually responsive and bursting with saccades, either spontaneous or visually triggered. The latencies of passive visual and VTEM responses to stimulus onset were comprised between 77 and 135 ms in 80% of the units. VTEM units also fired prior to retargeting saccades. Presaccadic units active with spontaneous saccades also discharged with visually elicited saccades. The earliest sign of activation after stimulus onset eliciting a saccade appeared between 80 and 100 ms, that is, in the same range of latencies as passive visual and VTEM units. Sustained visual responses consisted of activation in 18 units and inactivation in 26 units. The occurrence of these patterns of firing was related to stimulus fixation. In the majority of cases, the changes in discharge frequency started before fixation was achieved by a targeting saccade. They terminated before fixation was broken by a saccade away from the stimulus.(ABSTRACT TRUNCATED AT 400 WORDS)

Effect of passive eye movement on retinogeniculate transmission in the cat

1990 ◽  
Vol 63 (3) ◽  
pp. 523-538 ◽  
Author(s):  
R. Lal ◽  
M. J. Friedlander
Keyword(s):  
Firing Rate ◽  
Spontaneous Activity ◽  
Eye Movement ◽  
Visual Stimulus ◽  
Action Potentials ◽  
Visual Stimuli ◽  
Dorsal Lateral Geniculate Nucleus ◽  
Visual Response ◽  
Visual Responses ◽  
Movement Effect

1. The nature and time window of interaction between passive phasic eye movement signals and visual stimuli were studied for dorsal lateral geniculate nucleus (LGNd) neurons in the cat. Extracellular recordings were made from single neurons in layer A of the left LGNd of anesthetized paralyzed cats in response to a normalized visual stimulus presented to the right eye at each of several times of movement of the left eye. The left eye was moved passively at a fixed amplitude and velocity while varying the movement onset time with respect to the visual stimulus onset in a randomized and interleaved fashion. Visual stimuli consisted of square-wave modulated circular spots of appropriate contrast, sign, and size to elicit an optimal excitatory response when placed in the neurons' receptive-field (RF) center. 2. Interactions were analyzed for 78 neurons (33 X-neurons, 43 Y-neurons, and 2 physiologically unclassified neurons) on 25-65 trials of identical visual stimuli for each of eight times of eye movement. 3. Sixty percent (47/78) of the neurons tested had a significant eye movement effect (ANOVA, P less than 0.05) on some aspect of their visual response. Of these 47 neurons, 42 (89%) had a significant (P less than 0.05) effect of an appropriately timed eye movement on the number of action potentials, 36 (77%) had a significant effect on the mean peak firing rate, and 31 (66%) were significantly affected as evaluated by both criteria. 4. The eye movement effect on the neurons' visual responses was primarily facilitatory. Facilitation was observed for 37 (79%) of the affected neurons. For 25 of these 37 neurons (68%), the facilitation was significant (P less than 0.05) as evaluated by both criteria (number of action potentials and mean peak firing rate). Ten (21%) of the affected neurons had their visual response significantly inhibited (P less than 0.05). 5. Sixty percent (46/78) of the neurons were tested for the effect of eye movement on both visually elicited activity (visual stimulus contrast = 2 times threshold) and spontaneous activity (contrast = 0). Eye movement significantly affected the visual response of 23 (50%) of these neurons. However, spontaneous activity was significantly affected for only nine (20%) of these neurons. The interaction of the eye movement and visual signals was nonlinear. 6. Nine of 12 neurons (75%) tested had a directionally selective effect of eye movement on the visual response, with most (8/9) preferring the temporal ward direction.(ABSTRACT TRUNCATED AT 400 WORDS)

Target Selection for Saccadic Eye Movements: Direction-Selective Visual Responses in the Superior Colliculus

2001 ◽  
Vol 86 (5) ◽  
pp. 2527-2542 ◽  
Author(s):  
Gregory D. Horwitz ◽  
William T. Newsome
Keyword(s):  
Superior Colliculus ◽  
Eye Movement ◽  
Discrimination Task ◽  
Visual Motion ◽  
Target Selection ◽  
Small Population ◽  
Saccade Target ◽  
Visual Responses ◽  
Direction Discrimination ◽  
Deep Layers

We investigated the role of the superior colliculus (SC) in saccade target selection in rhesus monkeys who were trained to perform a direction-discrimination task. In this task, the monkey discriminated between opposed directions of visual motion and indicated its judgment by making a saccadic eye movement to one of two visual targets that were spatially aligned with the two possible directions of motion in the display. Thus the neural circuits that implement target selection in this task are likely to receive directionally selective visual inputs and be closely linked to the saccadic system. We therefore studied prelude neurons in the intermediate and deep layers of the SC that can discharge up to several seconds before an impending saccade, indicating a relatively high-level role in saccade planning. We used the direction-discrimination task to identify neurons whose prelude activity “predicted” the impending perceptual report several seconds before the animal actually executed the operant eye movement; these “choice predicting” cells comprised ∼30% of the neurons we encountered in the intermediate and deep layers of the SC. Surprisingly, about half of these prelude cells yielded direction-selective responses to our motion stimulus during a passive fixation task. In general, these neurons responded to motion stimuli in many locations around the visual field including the center of gaze where the visual discriminanda were positioned during the direction-discrimination task. Preferred directions generally pointed toward the location of the movement field of the SC neuron in accordance with the sensorimotor demands of the discrimination task. Control experiments indicate that the directional responses do not simply reflect covertly planned saccades. Our results indicate that a small population of SC prelude neurons exhibits properties appropriate for linking stimulus cues to saccade target selection in the context of a visual discrimination task.

Dodge-Ing the Issue: Dodge, Javal, Hering, and the Measurement of Saccades in Eye-Movement Research

Perception ◽  
10.1068/p3470 ◽  
2003 ◽  
Vol 32 (7) ◽  
pp. 793-804 ◽  
Author(s):  
Nicholas J Wade ◽  
Benjamin W Tatler ◽  
Dieter Heller
Keyword(s):  
Nineteenth Century ◽  
Twentieth Century ◽  
Eye Movements ◽  
Eye Movement ◽  
Eye Position ◽  
Type I ◽  
Rapid Eye Movements ◽  
Early Twentieth Century ◽  
Discontinuous Nature ◽  
Eye Movements During Reading

Dodge, in 1916, suggested that the French term ‘saccade’ should be used for describing the rapid movements of the eyes that occur while reading. Previously he had referred to these as type I movements. Javal had used the term ‘saccade’ in 1879, when describing experiments conducted in his laboratory by Lamare. Accordingly, Javal has been rightly credited with assigning the term to rapid eye movements. In English these rapid rotations had been called jerks, and they had been observed and measured before Lamare's studies of reading. Rapid sweeps of the eyes occur as one phase of nystagmus; they were observed by Wells in 1792 who used an afterimage technique, and they were illustrated by Crum Brown in 1878. Afterimages were used in nineteenth-century research on eye movements and eye position; they were also employed by Hering in 1879, to ascertain how the eyes moved during reading. In the previous year, Javal had employed afterimages in his investigations of reading, but this was to demonstrate that the eyes moved horizontally rather than vertically. Hering's and Lamare's auditory method established the discontinuous nature of eye movements during reading, and the photographic methods introduced by Dodge and others in the early twentieth century enabled their characteristics to be determined with greater accuracy.

An Illusion of Velocity in Motion Perception

1994 ◽  
Vol 78 (1) ◽  
pp. 112-114
Author(s):  
Kazuhito Noguchi ◽  
Koichi Haishi ◽  
Daisuke Sato
Keyword(s):  
Eye Movement ◽  
Motion Perception ◽  
Turning Point ◽  
Eye Position ◽  
Triangular Wave ◽  
Saccadic Movement ◽  
Ball Bouncing ◽  
The Subject

We report a phenomenon that seems to have potential to elucidate a role of eye movement in motion perception. When tracking a target controlled by a triangular wave, the viewer perceives movement of the target like a ball bouncing in between two walls. We measured eye movement with electrooculograms (EOGs) when the subject was tracking a target controlled by a triangular wave. Eye movement after passing the turning point and rapidly returning to the target with saccadic movement and then smoothly tracking the target was recorded for all 4 adults. It was considered that extraretinal information on eye position during saccade may mainly contribute to this illusion.

Sign in / Sign up

Export Citation Format

Share Document