Types Of Saccades Research Articles

Eye movement and visuomotor arm movement deficits following mild closed head injury

Based on increasing evidence that even mild closed head injury (CHI) can cause considerable neural damage throughout the brain, we hypothesized that mild CHI will disrupt the complex cerebral networks concerned with oculomotor and upper-limb visuomotor control, resulting in impaired motor function. Within 10 days following mild CHI (Glasgow Coma Scale 13-15, alteration of consciousness <20 min), we compared 30 patients (15-37 years) and 30 matched controls on different types of saccades, oculomotor smooth pursuit (sine and random), upper-limb visuomotor performance and several neuropsychological tests known to be sensitive to head trauma. Simple reflexive saccades were not impaired, whereas, on the antisaccade task, the CHI group demonstrated prolonged saccadic latencies, a marginally higher number of directional errors and poorer spatial accuracy. The CHI group exhibited more directional errors and impaired motor accuracy on memory-guided sequences of saccades and produced fewer self-paced saccades within 30 s. Most measures of sinusoidal and random oculomotor smooth pursuit showed no deficits, with the exception of a prolonged lag on random smooth pursuit in the CHI group. While arm movement reaction time and arm steadiness were not impaired, the CHI group showed decreased arm movement speed and decreased upper-limb motor accuracy. Conversely, after controlling for IQ, the CHI group had few head trauma-related neuropsychological deficits. These results indicate that multiple motor systems can be impaired following mild CHI and that this can occur independently of neuropsychological impairment. Our study also indicates that quantitative tests of oculomotor and upper-limb visuomotor function may provide sensitive markers of cerebral dysfunction, suggesting the potential use of such tests to supplement patient assessment. To our knowledge, this study is the first to demonstrate the presence of oculomotor or visuomotor deficits following mild CHI.

Inhibition of saccade return in reading

We examined the characteristics of readers’ eye movements as they read sentences or short passages of text and compared the durations of eye fixations preceding two types of saccades: (a) saccades to words that were fixated on the prior fixation (return saccades) and (b) saccades in which the eyes moved about the same distance but did not land on a word fixated on the prior fixation (non-return saccades). Consistent with research from much simpler attention or oculomotor tasks, we found what could be considered an inhibition of return effect: fixations preceding return saccades were longer than those preceding non-return saccades.

Differential cortical activation during voluntary and reflexive saccades in man

A saccade involves both a step in eye position and an obligatory shift in spatial attention. The traditional division of saccades into two types, the “reflexive” saccade made in response to an exogenous stimulus change in the visual periphery and the “voluntary” saccade based on an endogenous judgement to move gaze, is supported by lines of evidence which include the longer onset latency of the latter and the differential effects of lesions in humans and primates on each. It has been supposed that differences between the two types of saccade derive from differences in how the spatial attention shifts involved in each are processed. However, while functional imaging studies have affirmed the close link between saccades and attentional shifts by showing they activate overlapping cortical networks, attempts to contrast exogenous with endogenous (“covert”) attentional shifts directly have not revealed separate patterns of cortical activation. We took the “overt” approach, contrasting whole reflexive and voluntary saccades using event-related fMRI. This demonstrated that, relative to reflexive saccades, voluntary saccades produced greater activation within the frontal eye fields and the saccade-related area of the intraparietal sulci. The reverse contrast showed reflexive saccades to be associated with relative activation of the angular gyrus of the inferior parietal lobule, strongest in the right hemisphere. The frequent involvement of the right inferior parietal lobule in lesions causing hemispatial neglect has long implicated this parietal region in an important, though as yet uncertain, role in the awareness and exploration of space. This is the first study to demonstrate preferential activation of an area in its posterior part, the right angular gyrus, during production of exogenously triggered rather than endogenously generated saccades, a finding which we propose is consistent with an important role for the angular gyrus in exogenous saccadic orienting.

Voluntary spatial attention has different effects on voluntary and reflexive saccades.

Although numerous studies have investigated the relationship between saccadic eye movements and spatial attention, one fundamental issue remains controversial. Some studies have suggested that spatial attention facilitates saccades, whereas others have claimed that eye movements are actually inhibited when spatial attention is engaged. However, these discrepancies may be because previous research has neglected to separate and specify the effects of attention for two distinct types of saccades, namely reflexive (stimulus-directed) and voluntary (antisaccades). The present study explored the effects of voluntary spatial attention on both voluntary and reflexive saccades. Results indicate that voluntary spatial attention has different effects on the two types of saccades. Antisaccades were always greatly facilitated following the engagement of spatial attention by symbolic cues (arrows) informing the subject where the upcoming saccade should be directed. Reflexive saccades showed little or no cueing effects and exhibited significant facilitation only when these cues were randomly intermixed with uncued trials. In addition, the present study tested the effects of fixation condition (gap, step, and overlap) on attentional modulation. Cueing effects did not vary due to fixation condition. Thus, voluntary spatial attention consistently showed different effects on voluntary and reflexive saccades, and there was no evidence in these studies that voluntary cues inhibit reflexive saccades, even in a gap paradigm.

Oculomotor behaviour as a reflection of attention and memory processes: Neural mechanisms and applications to human factors

The present paper provides a review of the current state of knowledge on the neuroanatomical circuits underlying different types of eye movements, including prosaccades, antisaccades and memory-driven saccades. This is accomplished through a review of human lesion, neuroimaging and psychophysical studies. Research which has focused on the explication of the role of attentional and memory processes in oculomotor control is also reviewed and discussed. Finally, it is suggested how this knowledge might be applied in the study of a variety of different issues of relevance to human factors including display design, workload assessment, training and selection.

Expectation-based, multi-focal, saccadic (EMS) vision for ground vehicle guidance

Abstract The 'MarVEye' camera configuration realized with three to four conventional miniature CCD-TV-cameras mounted fix relative to each other on a high bandwidth pan-and-tilt platform is discussed. A saccadic type of vision with intermittent phases of fast saccades and smooth pursuit does complicate image sequence interpretation; however, with explicit spatio-temporal representations available in the 4-D approach this can be handled in a straightforward way. The newly developed machine vision system based on COTS-PC-hardware and object-oriented programming is described. Applications of this 'vertebrate'-type vision system in the field of road vehicle guidance are presented.

Quantitative analysis of catch-up saccades during sustained pursuit.

During visual tracking of a moving stimulus, primates orient their visual axis by combining two very different types of eye movements, smooth pursuit and saccades. The purpose of this paper was to investigate quantitatively the catch-up saccades occurring during sustained pursuit. We used a ramp-step-ramp paradigm to evoke catch-up saccades during sustained pursuit. In general, catch-up saccades followed the unexpected steps in position and velocity of the target. We observed catch-up saccades in the same direction as the smooth eye movement (forward saccades) as well as in the opposite direction (reverse saccades). We made a comparison of the main sequences of forward saccades, reverse saccades, and control saccades made to stationary targets. They were all three significantly different from each other and were fully compatible with the hypothesis that the smooth pursuit component is added to the saccadic component during catch-up saccades. A multiple linear regression analysis was performed on the saccadic component to find the parameters determining the amplitude of catch-up saccades. We found that both position error and retinal slip are taken into account in catch-up saccade programming to predict the future trajectory of the moving target. We also demonstrated that the saccadic system needs a minimum period of approximately 90 ms for taking into account changes in target trajectory. Finally, we reported a saturation (above 15 degrees /s) in the contribution of retinal slip to the amplitude of catch-up saccades.

Neural control of saccades

Quantitative models of the oculomotor plant and control of the saccadic eye movement system are presented in this chapter. Oculomotor plant models described here are linear, including a second-order model by Westheimer (1954), Bahill et al. (1980) and Enderle et al. (2000). The model of the saccade generator is initiated by the superior colliculus and terminated by the cerebellar fastigial nucleus that operates under a time optimal control strategy. A common mechanism for all types of saccades is described, including those with dynamic overshoot and glissadic behavior. Conflicting evidence exists regarding the operation of the excitatory burst neuron during saccades. The excitatory burst neuron operates within two states: complete inhibition, and without inhibition that is characterized by high firing at rates of up to 1000 Hz. While there is direct evidence of projections from the superior colliculus to the paramedian pontine reticular formation, there is conflictory evidence regarding the connections from the superior colliculus to the excitatory burst neuron, with the most recent experimental results supporting no direct connections. A model of the excitatory burst neuron is described using a Hodgkin-Huxley model of the neuron that fires at 1000 Hz automatically and without stimulation when released from inhibition. SIMULINK simulations using this neuron model have all of the characteristics of the excitatory burst neuron firing rate during a saccade. This model eliminates the need to introduce BIAS inputs that causes bursting in some models of the saccade generator. Such a model is also appropriate for modeling the Omnipause neurons.

Which duration of postsaccadic slowing identifies anticipatory saccades during smooth pursuit eye movements?

Increased frequency of anticipatory saccades during smooth pursuit eye movements is a potential marker of genetic risk for schizophrenia. Postsaccadic slowing criteria are used to separate anticipatory from other types of saccades. However, the necessary duration of slowed pursuit required to identify an anticipatory saccade remains undetermined. We explored the effect of various postsaccadic slowing duration criteria on effect size in a comparison of younger and older schizophrenic and normal adults. For large anticipatory saccades, varying the duration of postsaccadic slowing criteria did not notably change effect size. For smaller leading saccades, a limited 50-ms duration postsaccadic slowing criterion produced the largest effect size (1.54), and maintained a similar effect size across a broad age range. Leading saccades with a limited duration postsaccadic slowing criteria are a possible marker of genetic risk for schizophrenia.

Sakkaden

Saccades are fast, in the clinical sense conjugated eye movements. Their purpose is to bring the fovea to the visual targets. Different types of saccades can be distinguished. Thescientific discussion is mainly focussed on following questions: how does the brain do the necessary transformation of the retinal coordinates into craniotopic coordinates and whether the saccadic eye movements are primarily conjugated or disconjugated. The growing knowledge about the function of these structures allows topographic diagnosis to be applied to disorders of saccadic eye movements. In general, cortical disorders are distinguished by a prolonged saccadic reaction time. Frontal cortical lesions are specifically characterised by loss of suppression of unwanted saccades and disruption of saccades to remembered targets; parietal cortical lesions by disruption in the calculation of preceding saccades. Cerebellar lesions - posterior vermis and caudal fastigial nucleus - become manifest as dysmetric, hypermetrics saccades. Lesions of the pontine brainstem manifest as ipsiversive saccade paresis and slowing.

The Difference in Saccadic Parameters Among Several Visually Guided Tasks

Purpose: The present study was undertaken to establish the effects of the five different paradigms (simultaneous, gap, overlap, delayed-memory, and anti-saccade tasks) on saccade dynamics (duration, peak velocity, and amplitude). Methods: We recorded ocular movements in 7 normal subjects, using infrared oculography with a visual stimulation system. Results: The distribution of saccade accuracy in gap and overlap tasks had about the same steepness as that in simultaneous tasks, but that in delayed-memory and anti-saccade tasks was broader than that in simultaneous tasks. The distribution in anti-saccade tasks had a marked intersubject variability, and the average values of accuracy were hypermetric in four subjects. The peak velocity/amplitude ratio in simultaneous and gap tasks were higher than those of other tasks. The relationship between average of peak velocity of abduction and adduction was different, adduction was higher than abduction in simultaneous and gap tasks, and abduction was lower than adduction in delayed-memory and anti-saccade tasks. Conclusions: The dynamics in simultaneous tasks had about the same characteristics as in gap tasks, but were different from those in overlap, delayed-memory, and anti-saccade tasks. These results indicated that the marked differences in dynamic properties among different saccade types may reflect processes in the visuomotor system.

Spatial and temporal aspects of eye-hand coordination across different tasks.

The way in which saccadic eye movements are elicited influences their latency and accuracy. Accordingly, different tasks elicit different types of saccades. Using the tasks steps, gap, memory, scanning and antisaccade, we analyzed combined eye and hand movements to determine whether both motor systems share control strategies. Errors and latencies were measured to examine whether changes in eye motor behavior are reflected in hand motor behavior. Directional and variable errors of eye and hand changed differently according to the tasks. Moreover, errors of the two systems did not correlate for any of the tasks investigated. Contrary to errors, mean latencies of eye movements were organized in the same pattern as hand movements. A correlation of latencies indicates that both motor systems rely on common information to initiate movement. Temporal coupling was stronger for intentional tasks than for reflexive tasks.

Expectation-Based, Multi-Focal, Saccadic (EMS) Vision for Ground Vehicle Guidance

The 'MarVEye' camera configuration realized with three to four conventional miniature CCD-TV-cameras mounted fix relative to each other on a high bandwidth pan-and-tilt platform is discussed. A saccadic type of vision with intermittent phases of fast saccades and smooth pursuit does complicate image sequence interpretation; however, with explicit spatio-temporal representations available in the 4-D approach this can be handled in a straightforward way. The newly developed machine vision system based on COTS-PC-hardware and object-oriented programming is described. Applications of this 'vertebrate'-type vision system in the field of road vehicle guidance are presented.

Saccadic distractibility in first-episode schizophrenia

Early-life stress (ES) such as adoption, change of caregiver, or experience of emotional neglect may influence the way in which affected individuals respond to emotional stimuli of positive or negative valence. These modified responses may stem from a direct alteration of how emotional stimuli are coded, and/or the cognitive function implicated in emotion modulation, such as self-regulation or inhibition. These ES effects have been probed on tasks either targeting reward and inhibitory function. Findings revealed deficits in both reward processing and inhibitory control in ES youths. However, no work has yet examined whether incentives can improve automatic response or inhibitory control in ES youths.To determine whether incentives would only improve self-regulated voluntary actions or generalize to automated motoric responses, participants were tested on a mixed eye movement task that included reflex-like prosaccades and voluntary controlled antisaccade eye movements. Seventeen adopted children (10 females, mean age 11.3 years) with a documented history of neglect and 29 typical healthy youths (16 females, mean age 11.9 years) performed the mixed prosaccade/antisaccade task during monetary incentive conditions or during no-incentive conditions.Across both saccade types, ES adolescents responded more slowly than controls. As expected, control participants committed fewer errors on antisaccades during the monetary incentive condition relative to the no-incentive condition. By contrast, ES youths failed to show this incentive-related improvement on inhibitory control. No significant incentive effects were found with prepotent prosaccades trials in either group. Finally, co-morbid psychopathology did not modulate the findings.These data suggest that youths with experience of early stress exhibit deficient modulation of inhibitory control by reward processes, in tandem with a reward-independent deficit in preparation for both automatic and controlled responses. These data may be relevant to interventions in ES youths.

Cortical and subcortical influences on the nucleus of the optic tract of the opossum

In the present work we propose a new phylogenetic hypothesis for the role played by cortical and subcortical afferents to the nucleus of the optical tract, the main visual relay station of the horizontal optokinetic reflex in mammals. The hypothesis is supported by anatomical and physiological data obtained in the South American opossum ( Didelphis aurita) using the following experimental approaches: (i) single-unit recordings in the nucleus of the optic tract and simultaneous electrical stimulation of the contralateral nucleus of the optic tract; (ii) single-unit recordings in the nucleus of the optic tract and simultaneous electrical stimulation of the ipsilateral striate cortex; (iii) injection of cholera toxin subunit B into the striate cortex and subsequent immunohistochemical reaction to reveal the presence of the marker in the thalamus and mesencephalon; and (iv) single-unit recordings in the nucleus of the optic tract both before and after ablation of the ipsilateral visual cortex. The main results are: (i) there is a strong inhibitory reciprocal effect upon the nucleus of the optic tract following stimulation of its contralateral counterpart; (ii) electrophysiological and anatomical data imply that the visual cortex does not project directly to the nucleus of the optic tract. Rather, cortical terminals seem to target the nearby anterior and posterior pretectal nuclei and orthodromic latencies in the nucleus of the optic tract following stimulation of the visual cortex were twice as large as in the superior colicullus; and (iii) ablation of the entire visual cortex did not have any effect upon binocularity of cells in the nucleus of the optic tract. These results strengthen the model proposed here for the role of the interactions between the nuclei of the optic tract under optokinetic stimulation. The hypothesis in the present work is that the cortical influences upon the nucleus of the optical tract, in addition to the subcortical ones, appeared only recently in phylogenesis. In more primitive mammals, such as the opossum, subcortical interactions are thought to play a relatively important role. With the emergence of retinal specializations, such as the fovea, one might suppose that there followed the appearance of new ocular movements, such as the smooth pursuit and certain types of saccades, that came to join the pre-existent optokinetic reflex.

Express averaging saccades in monkeys

When monkeys are presented simultaneously with multiple stimuli, they can make one of two types of response. Either they make averaging saccades, that land at intermediate locations between the targets, or target-directed saccades, that land close to one of the targets. The two types of saccades occur at different latencies and are thought to reflect different processes; fast reflexive averaging and slower target selection. We investigated the latency of averaging saccades in five monkeys, with particular emphasis on ‘express’ latency saccades, which are thought to be inhibited by target selection. Express averaging saccades were made prolifically by the two monkeys that made both express and regular latency saccades, but only when no specific instruction was given regarding the saccade target. When these monkeys had to choose one of the targets, on the basis of its color, they still made averaging saccades. However, the endpoints formed two distributions close to the targets as opposed to one single distribution centered between the targets, as was the case when targets were identical; also, express saccades were almost entirely absent. We conclude that express averaging saccades are a form of spatial and temporal optimization of gaze shifting.

Electroencephalographic cortical oscillations and saccadic eye movements in humans

A model predicting different types of saccades has suggested that the presence of rhythmic brain activity determines whether a subject will produce regular or express saccades. We studied cortical oscillations preceding saccadic eye movements. Brain electrical activity was recorded in nine healthy adults continuously from 30 electrodes while subjects performed saccades. In a so-called gap condition multimodal latency distributions resulted. Express saccades were preceded by different oscillatory activity than regular saccades. This was a highly significant finding restricted to the alpha and beta bands of the EEG. Step-wise discriminant analysis showed that cortical oscillations measured from only few electrode sites allowed to predict reliably which type of saccade a subject will make. These findings support the notion that stimulus-induced oscillations of the human EEG may modulate thresholds for triggering saccades.

Presaccadic omnidirectional burst activity in the basal interstitial nucleus in the monkey cerebellum.

We recorded saccade-related neurons in the vicinity of the dentate nucleus of the cerebellum in two monkeys trained to perform visually guided saccades and memory-guided saccades. Among 76 saccade-related neurons, 38 showed presaccadic bursts in all directions. More than 80% of such burst neurons were located in the area ventral to, not inside, the dentate nucleus, which corresponded to the basal interstitial nucleus (BIN as previously described). We found that the activity of the BIN neurons was correlated with saccade duration but not with saccade amplitude or velocity. Thus, when tested with visually guided saccades, the burst started about 16 ms before saccade onset and ended about 33 ms before saccade offset, regardless of saccade amplitude. The characteristic timing of the BIN cell activity was maintained for different types of saccades (visually guided, memory-guided and spontaneous saccades), which had different dynamics. Although the number of spikes in a burst for each neuron was linearly correlated with saccade amplitude for a given type of saccade, the slope varied depending on the type of saccade. Peak burst frequency was uncorrelated with saccadic peak velocity. In contrast, burst duration was highly correlated with saccade duration regardless of the type of saccade. These results suggest that BIN neurons may carry information to determine the timing of saccades.

Saccadic velocity and activation: development of a diagnostic tool for assessing energy regulation

The hypothesis was tested that peak velocity of saccadic eye movements in visual motor tasks varies with variables related to energy regulation. The hypothesis is based on the cognitive-energetical performance model of Sanders. An experimental paradigm was developed in which saccadic peak velocity of task-relevant eye movements is measured while a choice reaction task is carried out. Confounding factors of saccadic amplitude and movement direction were controlled. The task was designed in such a way that in each trial subjects performed a target saccade towards an imperative stimulus and a return saccade after the manual response back to the centre of the screen. For both types of saccades the experimental variables were foreperiod duration (short versus long), knowledge of results (with versus without), postsaccadic demand (low versus high) and time on task (five 30-min intervals). In two experiments, there are main and interaction effects of the task variables on peak saccadic velocity. Return saccades are slower than target saccades, but not in the case of high postsaccadic demand. Knowledge of results increases peak saccadic velocity, but more so for return than for target saccades. Time on task leads to a decrease in peak saccadic velocity, which is much stronger for return than for target saccades; furthermore this effect is more pronounced after short than after long foreperiods. Peak saccadic velocity is changed within seconds. The results support the hypothesis. Peak saccadic velocity of task related eye movements reflects energy regulation during task performance. The paradigm will be developed as a diagnostic tool in workload measurement.

Ocular motor abnormalities in Huntington's disease

We review here the eye movements in patients with Huntington's disease (HD), concentrating upon saccades as they show the most prominent abnormalities. Inability to suppress reflexive glances to suddenly appearing novel visual stimuli and delayed initiation of voluntary saccades, including predictive saccades, are early and consistent findings. These two abnormalities can be interpreted in the context of a model, based upon the idea that the frontal lobes and basal ganglia contribute more to the control of voluntary than to reflexive types of saccades. Most patients eventually also show slow saccades but they are most prominent when the disease is early-onset. Slowing of saccades may reflect involvement of both the higher-level cerebral centers that trigger saccades and the areas in the brain stem that produce premotor saccade commands. The study of eye movements in HD has led to a fruitful interaction between basic science and clinical investigation, and has served as a paradigm for examining higher-level defects in saccadic eye movement control in patients with various degenerative, neurological diseases or with focal cerebral hemispheral lesions.