scholarly journals Eye movements during visuomotor adaptation represent only part of the explicit learning

2019 ◽  
Author(s):  
Zohar Bromberg ◽  
Opher Donchin ◽  
Shlomi Haar

AbstractVisuomotor rotations are learned through a combination of explicit strategy and implicit recalibration. However, measuring the relative contribution of each remains a challenge and the possibility of multiple explicit and implicit components complicates the issue. Recent interest has focused on the possibility that eye movements reflect explicit strategy. Here we compared eye movements during adaptation to two accepted measures of explicit learning - verbal report and the exclusion test. We found that while reporting, all subjects showed a match between all three measures. However, when subjects did not report their intention, the eye movements of some subjects suggested less explicit adaptation than what was measured in an exclusion test. Interestingly, subjects whose eye movements did match their exclusion could be clustered into two subgroups: fully implicit learners showing no evidence of explicit adaptation and explicit learners with little implicit adaptation. Subjects showing a mix of both explicit and implicit adaptation were also those where eye movements showed less explicit adaptation than did exclusion. Thus, our results support the idea of multiple components of explicit learning as only part of the explicit learning is reflected in the eye movements. Individual subjects may use explicit components that are reflected in the eyes or those that are not or some mixture of the two. Analysis of reaction times suggests that the explicit components reflected in the eye-movements involve longer reaction times. This component, according to recent literature, may be related to mental rotation.Significance StatementVisuomotor adaptation involves both explicit and implicit components: aware re-aiming and unaware error correction. Recent studies suggest that eye movements could be used to capture the explicit component, a method that would have significant advantages over other approaches. We show that eye movements capture only one component of explicit adaptation. This component scales with reaction time while the component unrelated to eye movements does not. Our finding has obvious practical implications for the use of eye movements as a proxy for explicit learning. However, our results also corroborate recent findings suggesting the existence of multiple explicit components, and, specifically, their decomposition into components correlated with reaction time and components that are not.

2016 ◽  
Vol 9 (5) ◽  
Author(s):  
Aleksandra Kroll ◽  
Monika Mak ◽  
Jerzy Samochowiec

Reaction times are often used as an indicator of the efficiency of the processes in thecentral nervous system. While extensive research has been conducted on the possibleresponse time correlates, the role of eye movements in visual tasks is yet unclear. Here wereport data to support the role of eye movements during visual choice reaction time training.Participant performance, reaction times, and total session duration improved. Eyemovementsshowed expected changes in saccade amplitude and resulted in improvementin visual target searching.


Author(s):  
Srdan Medimorec ◽  
Petar Milin ◽  
Dagmar Divjak

Abstract. Implicit sequence learning is an integral part of human experience, yet the nature of the mechanisms underlying this type of learning remains a matter of debate. In the current study, we provide a test for two accounts of implicit sequence learning, that is, one that highlights sequence learning in the absence of any motor responses (with suppressed eye movements) and one that highlights the relative contribution of the motor processes (i.e., eye movements) to learning. To adjudicate between these accounts and determine whether a motor response is a requisite process in sequence learning, we used anticipation measures to compare performance on the standard oculomotor serial reaction time (SRT) task and on a version of the SRT task where the eye movements were restricted during the learning phase. our results demonstrated an increased proportion of correct anticipations in the standard SRT task compared to the restricted-movement task.


1999 ◽  
Vol 13 (3) ◽  
pp. 145-151 ◽  
Author(s):  
Andrew Smith ◽  
Neil Rich ◽  
Wendy Sturgess ◽  
Carolyn Brice ◽  
Claire Collison ◽  
...  

Abstract The present study examined whether volunteers with common colds showed impairments in objective and subjective indicators of alertness. All the volunteers (N = 81) were tested when healthy to provide baseline data for mood, simple and choice reaction time tasks, and an anti-saccadic eye movement task. When subjects developed a cold (N = 17) they returned to the laboratory and repeated the procedure. Volunteers (N = 64) who remained healthy over a 10-week period were recalled as controls. The results showed that those with colds felt significantly less alert and had significantly slower simple and choice reaction times and eye movements. This extends earlier research and shows that electrophysiological measures may also be of use in assessing the behavioral changes induced by upper respiratory tract illnesses.


2019 ◽  
Vol 121 (4) ◽  
pp. 1478-1490 ◽  
Author(s):  
Eva-Maria Reuter ◽  
Welber Marinovic ◽  
Timothy N. Welsh ◽  
Timothy J. Carroll

The characteristics of movements are strongly history-dependent. Marinovic et al. (Marinovic W, Poh E, de Rugy A, Carroll TJ. eLife 6: e26713, 2017) showed that past experience influences the execution of limb movements through a combination of temporally stable processes that are strictly use dependent and dynamically evolving and context-dependent processes that reflect prediction of future actions. Here we tested the basis of history-dependent biases for multiple spatiotemporal features of saccadic eye movements under two preparation time conditions (long and short). Twenty people performed saccades to visual targets. To prompt context-specific expectations of most likely target locations, 1 of 12 potential target locations was specified on ~85% of the trials and each remaining target was presented on ~1% trials. In long preparation trials participants were shown the location of the next target 1 s before its presentation onset, whereas in short preparation trials each target was first specified as the cue to move. Saccade reaction times and direction were biased by recent saccade history but according to distinct spatial tuning profiles. Biases were purely expectation related for saccadic reaction times, which increased linearly as the distance from the repeated target location increased when preparation time was short but were similar to all targets when preparation time was long. By contrast, the directions of saccades were biased toward the repeated target in both preparation time conditions, although to a lesser extent when the target location was precued (long preparation). The results suggest that saccade history affects saccade dynamics via both use- and expectation-dependent mechanisms and that movement history has dissociable effects on reaction time and saccadic direction. NEW & NOTEWORTHY The characteristics of our movements are influenced not only by concurrent sensory inputs but also by how we have moved in the past. For limb movements, history effects involve both use-dependent processes due strictly to movement repetition and processes that reflect prediction of future actions. Here we show that saccade history also affects saccade dynamics via use- and expectation-dependent mechanisms but that movement history has dissociable effects on saccade reaction time and direction.


1998 ◽  
Vol 86 (1) ◽  
pp. 79-84 ◽  
Author(s):  
Karl Schweizer

The contributions of visual search to reaction time and cognitive ability were investigated with 45 subjects. Visual search was assessed via eye movements. The electrooculogram was recorded while a subject located letters arranged in a large display. Reaction time was obtained for a search task. A reasoning and a space scale served to assess cognitive ability. Substantial correlations of number, amplitude, and velocity of saccades with reaction time were obtained. Significant correlations of scores on ability scales with reaction times and amplitudes of saccades were also observed. Obviously, subjects of higher ability showed amplitudes better adjusted to the distances between the letters than those of lower ability.


eNeuro ◽  
2019 ◽  
Vol 6 (6) ◽  
pp. ENEURO.0308-19.2019 ◽  
Author(s):  
Zohar Bromberg ◽  
Opher Donchin ◽  
Shlomi Haar

2014 ◽  
Vol 36 (5) ◽  
pp. 506-515 ◽  
Author(s):  
Chris Englert ◽  
Alex Bertrams

In the current study, we consider that optimal sprint start performance requires the self-control of responses. Therefore, start performance should depend on athletes’ self-control strength. We assumed that momentary depletion of self-control strength (ego depletion) would either speed up or slow down the initiation of a sprint start, where an initiation that was sped up would carry the increased risk of a false start. Applying a mixed between- (depletion vs. nondepletion) and within- (before vs. after manipulation of depletion) subjects design, we tested the start reaction times of 37 sport students. We found that participants’ start reaction times decelerated after finishing a depleting task, whereas it remained constant in the nondepletion condition. These results indicate that sprint start performance can be impaired by unrelated preceding actions that lower momentary self-control strength. We discuss practical implications in terms of optimizing sprint starts and related overall sprint performance.


Perception ◽  
1993 ◽  
Vol 22 (5) ◽  
pp. 509-515 ◽  
Author(s):  
Jukka Saarinen

Pattern discrimination in the presence of distractor patterns is improved when the stimulus display is preceded by a precue designating the location of the target pattern. Experiments were conducted to determine how big an improvement the precue produced. The specific question of whether the observer is able to process selectively the stimulus pattern in the cued location of the display and ignore the patterns of the noncued locations was addressed. In order to study this, reaction time for pattern discrimination on a blank background (no distractors) was compared with the reaction time when the observer performed the same discrimination task in the presence of distractors and a precue had indicated the location of the stimulus pattern to be discriminated. The results showed that these two reaction times were equal if the cue preceded the stimulus patterns at intervals which were longer than some minimum time. Hence, stimuli outside the ‘aperture’ of focal attention can be ignored. These results could not be attributed to eye movements, because the longest duration of the whole sequence of precue and stimulus patterns was only 200 ms.


GeroPsych ◽  
2011 ◽  
Vol 24 (4) ◽  
pp. 169-176 ◽  
Author(s):  
Philippe Rast ◽  
Daniel Zimprich

In order to model within-person (WP) variance in a reaction time task, we applied a mixed location scale model using 335 participants from the second wave of the Zurich Longitudinal Study on Cognitive Aging. The age of the respondents and the performance in another reaction time task were used to explain individual differences in the WP variance. To account for larger variances due to slower reaction times, we also used the average of the predicted individual reaction time (RT) as a predictor for the WP variability. Here, the WP variability was a function of the mean. At the same time, older participants were more variable and those with better performance in another RT task were more consistent in their responses.


2006 ◽  
Vol 20 (3) ◽  
pp. 186-194 ◽  
Author(s):  
Susanne Mayr ◽  
Michael Niedeggen ◽  
Axel Buchner ◽  
Guido Orgs

Responding to a stimulus that had to be ignored previously is usually slowed-down (negative priming effect). This study investigates the reaction time and ERP effects of the negative priming phenomenon in the auditory domain. Thirty participants had to categorize sounds as musical instruments or animal voices. Reaction times were slowed-down in the negative priming condition relative to two control conditions. This effect was stronger for slow reactions (above intraindividual median) than for fast reactions (below intraindividual median). ERP analysis revealed a parietally located negativity of the negative priming condition compared to the control conditions between 550-730 ms poststimulus. This replicates the findings of Mayr, Niedeggen, Buchner, and Pietrowsky (2003) . The ERP correlate was more pronounced for slow trials (above intraindividual median) than for fast trials (below intraindividual median). The dependency of the negative priming effect size on the reaction time level found in the reaction time analysis as well as in the ERP analysis is consistent with both the inhibition as well as the episodic retrieval account of negative priming. A methodological artifact explanation of this effect-size dependency is discussed and discarded.


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