Saccadic Eye Movements of Dyslexic and Normal Reading Children

Perception ◽  
1994 ◽  
Vol 23 (1) ◽  
pp. 45-64 ◽  
Author(s):  
Monica Biscaldi ◽  
Burkhart Fischer ◽  
Franz Aiple
Keyword(s):  
Eye Movements ◽  
Reaction Times ◽  
Saccadic Eye Movements ◽  
Control Group ◽  
Express Saccades ◽  
Movement Data ◽  
Fixation Durations ◽  
Normal Reading ◽  
Single Target ◽  
The Right

Twenty-four children made saccades in five noncognitive tasks. Two standard tasks required saccades to a single target presented randomly 4 deg to the right or left of a fixation point. Three other tasks required sequential saccades from the left to the right. 75 parameters of the eye-movement data were collected for each child. On the basis of their reading, writing, and other cognitive performances, twelve children were considered dyslexic and were divided into two groups (D1 and D2). Group statistical comparisons revealed significant differences between control and dyslexic subjects. In general, in the standard tasks the dyslexic subjects had poorer fixation quality, failed more often to hit the target at once, had smaller primary saccades, and had shorter reaction times to the left as compared with the control group. The control group and group D1 dyslexics showed an asymmetrical distribution of reaction times, but in opposite directions. Group D2 dyslexics made more anticipatory and express saccades, they undershot the target more often in comparison with the control group, and almost never overshot it. In the sequential tasks group D1 subjects made fewer and larger saccades in a shorter time and group D2 subjects had shorter fixation durations than the subjects of the control group.

scholarly journals Express saccades and superior colliculus responses are sensitive to short-wavelength cone contrast

2016 ◽  
Vol 113 (24) ◽  
pp. 6743-6748 ◽  
Author(s):  
Nathan J. Hall ◽  
Carol L. Colby
Keyword(s):  
Eye Movements ◽  
Superior Colliculus ◽  
Short Wavelength ◽  
Human Subjects ◽  
Reaction Times ◽  
Saccadic Eye Movements ◽  
Express Saccades ◽  
Color Information ◽  
Express Saccade ◽  
Psychophysical Studies

A key structure for directing saccadic eye movements is the superior colliculus (SC). The visual pathways that project to the SC have been reported to carry only luminance information and not color information. Short-wavelength–sensitive cones (S-cones) in the retina make little or no contribution to luminance signals, leading to the conclusion that S-cone stimuli should be invisible to SC neurons. The premise that S-cone stimuli are invisible to the SC has been used in numerous clinical and human psychophysical studies. The assumption that the SC cannot use S-cone stimuli to guide behavior has never been tested. We show here that express saccades, which depend on the SC, can be driven by S-cone input. Further, express saccade reaction times and changes in SC activity depend on the amount of S-cone contrast. These results demonstrate that the SC can use S-cone stimuli to guide behavior. We conclude that the use of S-cone stimuli is insufficient to isolate SC function in psychophysical and clinical studies of human subjects.

scholarly journals WALD-EM: Wald Accumulation for Locations and Durations of Eye Movements

2020 ◽  
Author(s):  
Šimon Kucharský ◽  
Daan Roelof van Renswoude ◽  
Maartje Eusebia Josefa Raijmakers ◽  
Ingmar Visser
Keyword(s):  
Eye Movements ◽  
Eye Movement ◽  
Empirical Research ◽  
Process Models ◽  
Movement Behavior ◽  
Movement Data ◽  
Fixation Durations ◽  
Research Cycle ◽  
Fixation Locations ◽  
Basic Characteristics

Describing, analyzing and explaining patterns in eye movement behavior is crucial for understanding visual perception. Further, eye movements are increasingly used in informing cognitive process models. In this article, we start by reviewing basic characteristics and desiderata for models of eye movements. Specifically, we argue that there is a need for models combining spatial and temporal aspects of eye-tracking data (i.e., fixation durations and fixation locations), that formal models derived from concrete theoretical assumptions are needed to inform our empirical research, and custom statistical models are useful for detecting specific empirical phenomena that are to be explained by said theory. In this article, we develop a conceptual model of eye movements, or specifically, fixation durations and fixation locations, and from it derive a formal statistical model --- meeting our goal of crafting a model useful in both the theoretical and empirical research cycle. We demonstrate the use of the model on an example of infant natural scene viewing, to show that the model is able to explain different features of the eye movement data, and to showcase how to identify that the model needs to be adapted if it does not agree with the data. We conclude with discussion of potential future avenues for formal eye movement models.

scholarly journals Normal correspondence of tectal maps for saccadic eye movements in strabismus

2016 ◽  
Vol 116 (6) ◽  
pp. 2541-2549 ◽  
Author(s):  
John R. Economides ◽  
Daniel L. Adams ◽  
Jonathan C. Horton
Keyword(s):  
Electrical Stimulation ◽  
Eye Movements ◽  
Superior Colliculus ◽  
Saccadic Eye Movements ◽  
Systematic Change ◽  
Free Viewing ◽  
Pattern Deviation ◽  
Ocular Deviation ◽  
The Right ◽  
Stem Structure

The superior colliculus is a major brain stem structure for the production of saccadic eye movements. Electrical stimulation at any given point in the motor map generates saccades of defined amplitude and direction. It is unknown how this saccade map is affected by strabismus. Three macaques were raised with exotropia, an outwards ocular deviation, by detaching the medial rectus tendon in each eye at age 1 mo. The animals were able to make saccades to targets with either eye and appeared to alternate fixation freely. To probe the organization of the superior colliculus, microstimulation was applied at multiple sites, with the animals either free-viewing or fixating a target. On average, microstimulation drove nearly conjugate saccades, similar in both amplitude and direction but separated by the ocular deviation. Two monkeys showed a pattern deviation, characterized by a systematic change in the relative position of the two eyes with certain changes in gaze angle. These animals' saccades were slightly different for the right eye and left eye in their amplitude or direction. The differences were consistent with the animals' underlying pattern deviation, measured during static fixation and smooth pursuit. The tectal map for saccade generation appears to be normal in strabismus, but saccades may be affected by changes in the strabismic deviation that occur with different gaze angles.

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.

Saccadic eye movements and finger reaction times of table tennis players of different levels

2000 ◽  
Vol 24 (2) ◽  
pp. 335-338 ◽  
Author(s):  
Matthieu Lenoir ◽  
Luc Crevits ◽  
Maarten Goethals ◽  
Peter Duyck ◽  
Joanne Wildenbeest ◽  
...  
Keyword(s):  
Eye Movements ◽  
Reaction Times ◽  
Saccadic Eye Movements ◽  
Table Tennis ◽  
Tennis Players ◽  
Different Levels

scholarly journals Balance Markers and Saccadic Eye-Movement Measures in Adolescents With Postconcussion Syndrome

2020 ◽  
Vol 55 (5) ◽  
pp. 475-481 ◽  
Author(s):  
Coralie Rochefort ◽  
Elizabeth Legace ◽  
Chadwick Boulay ◽  
Gail Macartney ◽  
Kristian Goulet ◽  
...  
Keyword(s):  
Eye Movements ◽  
Cognitive Load ◽  
Effect Size ◽  
Dual Task ◽  
Postural Sway ◽  
Center Of Pressure ◽  
Saccadic Eye Movements ◽  
Control Group ◽  
Oculomotor Function ◽  
Anterior Posterior

Context Deficits in both balance and oculomotor function, including impairments in saccadic eye movements, are observed in approximately 30% of patients postconcussion. Whereas balance and saccadic eye movements are routinely assessed separately, growing evidence suggests that they should be assessed concurrently. Objective To compare balance measures and saccades between adolescents 1 to 3 months postconcussion and healthy uninjured adolescents. Design Case-control study. Setting Concussion clinic and 2 private schools. Patients or Other Participants Twenty-five adolescents (10 boys, 15 girls; median [interquartile range (IQR)] age = 14 years [11.5–16 years]) between 1 and 3 months postconcussion (median [IQR] time since injury = 39.5 days [30–56.75 days]) and 33 uninjured adolescents (18 boys, 15 girls; median [IQR] age = 13 years [11.5–14 years]). Main Outcome Measure(s) The center-of-pressure 95% ellipse area and medial-lateral and anterior-posterior velocity and the number of saccades in the dual-task balance conditions including a high cognitive load (cognitive condition), a low cognitive load and a gaze-shifting component (visual condition) or both a high cognitive load and a gaze-shifting component (combined condition). Results Concussion-group participants swayed over larger center-of-pressure ellipse areas in the visual (P = .02; effect size = 0.73) and combined (P = .005; effect size = 0.86) conditions but not in the cognitive condition (P = .07; effect size = 0.50). No group differences were identified for anterior-posterior (F1,56 = 2.57, P = .12) or medial-lateral (F1,56 = 0.157, P = .69) velocity. Concussion-group participants also did not perform more saccades than the control-group participants (F1,56 = 2.04, P = .16). Conclusions Performing dual-task balance conditions for which the secondary task involved a gaze-shifting component or both a gaze-shifting component and a high cognitive load resulted in greater sway amplitude in adolescents with concussion. However, these larger amounts of postural sway were not associated with increased saccadic eye movements.

Properties of Horizontal Saccades Accompanied by Blinks

1998 ◽  
Vol 79 (6) ◽  
pp. 2895-2902 ◽  
Author(s):  
Klaus G. Rottach ◽  
Vallabh E. Das ◽  
Walter Wohlgemuth ◽  
Ari Z. Zivotofsky ◽  
R. John Leigh
Keyword(s):  
Eye Movements ◽  
Peak Velocity ◽  
Dynamic Properties ◽  
Human Subjects ◽  
Saccadic Eye Movements ◽  
Stationary Target ◽  
Normal Human ◽  
The Right ◽  
Straight Ahead ◽  
Omnipause Neurons

Rottach, Klaus G., Vallabh E. Das, Walter Wohlgemuth, Ari Z. Zivotofsky, and R. John Leigh. Properties of horizontal saccades accompanied by blinks. J. Neurophysiol. 79: 2895–2902, 1998. Using the magnetic search coil technique to record eye and lid movements, we investigated the effect of voluntary blinks on horizontal saccades in five normal human subjects. The main goal of the study was to determine whether changes in the dynamics of saccades with blinks could be accounted for by a superposition of the eye movements induced by blinks as subjects fixated a stationary target and saccadic movements made without a blink. First, subjects made voluntary blinks as they fixed on stationary targets located straight ahead or 20° to the right or left. They then made saccades between two continuously visible targets 20 or 40° apart, while either attempting not to blink, or voluntarily blinking, with each saccade. During fixation of a target located straight ahead, blinks induced brief downward and nasalward deflections of eye position. When subjects looked at targets located at right or left 20°, similar initial movements were made by four of the subjects, but the amplitude of the adducted eye was reduced by 65% and was followed by a larger temporalward movement. Blinks caused substantial changes in the dynamic properties of saccades. For 20° saccades made with blinks, peak velocity and peak acceleration were decreased by ∼20% in all subjects compared with saccades made without blinks. Blinks caused the duration of 20° saccades to increase, on average, by 36%. On the other hand, blinks had only small effects on the gain of saccades. Blinks had little influence on the relative velocities of centrifugal versus centripetal saccades, and abducting versus adducting saccades. Three of five subjects showed a significantly increased incidence of dynamic overshoot in saccades accompanied by blinks, especially for 20° movements. Taken with other evidence, this finding suggests that saccadic omnipause neurons are inhibited by blinks, which have longer duration than the saccades that company them. In conclusion, the changes in dynamic properties of saccades brought about by blinks cannot be accounted for simply by a summation of gaze perturbations produced by blinks during fixation and saccadic eye movements made without blinks. Our findings, especially the appearance of dynamic overshoots, suggest that blinks affect the central programming of saccades. These effects of blinks need to be taken into account during studies of the dynamic properties of saccades.

Express saccades and visual attention

1993 ◽  
Vol 16 (3) ◽  
pp. 553-567 ◽  
Author(s):  
B. Fischer ◽  
H. Weber
Keyword(s):  
Eye Movements ◽  
Visual Attention ◽  
Reaction Times ◽  
Express Saccades ◽  
Research Groups ◽  
Express Saccade ◽  
Brain Functions ◽  
Target Article ◽  
Higher Brain Functions ◽  
Present Understanding

AbstractOne of the most intriguing and controversial observations in oculomotor research in recent years is the phenomenon of express saccades in monkeys and man. These are saccades with such short reaction times (100 msec in man, 70 msec in monkeys) that some experts on eye movements still regard them as artifacts or as anticipatory reactions that do not need any further explanation. On the other hand, some research groups consider them not only authentic but also a valuable means of investigating the mechanisms of saccade generation, the coordination of vision and eye movements, and the mechanisms of visual attention.This target article puts together pieces of experimental evidence in oculomotor and related research – with special emphasis on the express saccade – to enhance our present understanding of the coordination of vision, visual attention, and the eye movements subserving visual perception and cognition.We hypothesize that an optomotor reflex is responsible for the occurrence of express saccades, one that is controlled by higher brain functions involved in disengaged visual attention and decision making. We propose a neural network as the basis for more elaborate mathematical models or computer simulations of the optomotor system in primates.

Nigrostriatal Dopamine System in Learning to Perform Sequential Motor Tasks in a Predictive Manner

1999 ◽  
Vol 82 (2) ◽  
pp. 978-998 ◽  
Author(s):  
Naoyuki Matsumoto ◽  
Toru Hanakawa ◽  
Shinichiro Maki ◽  
Ann M. Graybiel ◽  
Minoru Kimura
Keyword(s):  
Eye Movements ◽  
Reaction Times ◽  
Saccadic Eye Movements ◽  
Nigrostriatal System ◽  
Initial Reaction ◽  
Dopamine Depletion ◽  
Motor Tasks ◽  
Push Button ◽  
Nigrostriatal Dopamine ◽  
Serial Reaction

Neurons in the primate striatum and the substantia nigra pars compacta change their firing patterns during sensory-motor learning. To study the consequences of nigrostriatal dopamine depletion for learning and memory of motor sequences, we used a neurotoxin, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), to deplete dopamine unilaterally in the striatum of macaque monkeys either before or after training them on sequential push-button motor tasks. We compared the monkeys’ performance with the arms ipsilateral and contralateral to dopamine depletion. During training and retraining on the tasks, we measured initial and serial movement times and reaction times for the push button movements, electromyographic patterns of arm and orofacial muscle activity during button pushing and reward licking, and saccadic eye movements during the button push sequences. With the arm ipsilateral to the side of dopamine depletion, each monkey showed progressive shortening of movement times and initial and serial reaction times, and each developed consistent strategies of hand-orofacial and hand-eye coordination in which single button push movements were linked efficiently to succeeding movements so that performance of the whole sequence became predictive. These patterns did not develop for contralateral arm performance in this monkey treated with MPTP before training. With the arm contralateral to dopamine depletion, the monkey showed significant quantitative deficits in all parameters measured except initial reaction times. Movement times and serial reaction times were longer than those for the ipsilateral arm; anticipatory saccadic eye movements were not well time-locked to individual button pushes made with the contralateral hand; and push and licking movements were not smoothly coordinated. This monkey further showed striking differences in performance when using the ipsilateral and contralateral arms in switch trial tests in which reward was delivered unexpectedly one button early. He continued to make movements to the previously rewarded button with the ipsilateral arm but showed no such automatic movements when he used his contralateral arm. For the monkey treated with MPTP after training, performance on the push-button task was skilled for both arms before dopamine depletion, but the unilateral dopamine depletion produced deficits in contralateral arm performance for all parameters measured, again excepting initial reaction times. With retraining, however, his performance with the contralateral arm improved. We conclude that the striatum and its nigrostriatal afferents function in the initial learning underlying performance of sequences of movements as single motor programs. The nigrostriatal system also operates during the retrieval of these programs once learning is accomplished, but lesions of the nigrostriatal system spare the ability to relearn the previously acquired programs.

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