Evidence map›Paper›PMID 28202573›Full record

ArticleJournal of neurophysiology2017

Alteration of the microsaccadic velocity-amplitude main sequence relationship after visual transients: implications for models of saccade control.

Antimo Buonocore, Chih-Yang Chen, Xiaoguang Tian, Saad Idrees, Thomas A Münch, Ziad M Hafed

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Article
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  14. Learning to silence saccadic suppression.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Review
  16. Task-Irrelevant Visual Forms Facilitate Covert and Overt Spatial Selection.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  17. Article
  18. Article
  19. Memory-guided microsaccades.Nature communications · 2019
    Article
  20. Eye Position Error Influence over "Open-Loop" Smooth Pursuit Initiation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Antimo BuonocoreWerner Reichardt Centre for Integrative Neuroscience, Tübingen University, Tübingen, Germany; antimo.buonocore@cin.uni-tuebingen.de.
Chih-Yang ChenWerner Reichardt Centre for Integrative Neuroscience, Tübingen University, Tübingen, Germany.
Xiaoguang TianWerner Reichardt Centre for Integrative Neuroscience, Tübingen University, Tübingen, Germany.
Saad IdreesWerner Reichardt Centre for Integrative Neuroscience, Tübingen University, Tübingen, Germany.
Thomas A MünchWerner Reichardt Centre for Integrative Neuroscience, Tübingen University, Tübingen, Germany.
Ziad M HafedWerner Reichardt Centre for Integrative Neuroscience, Tübingen University, Tübingen, Germany.ORCID 0000-0001-9968-119X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microsaccades occur during gaze fixation to correct for miniscule foveal motor errors. The mechanisms governing such fine oculomotor control are still not fully understood. In this study, we explored microsaccade control by analyzing the impacts of transient visual stimuli on these movements' kinematics. We found that such kinematics can be altered in systematic ways depending on the timing and spatial geometry of visual transients relative to the movement goals. In two male rhesus macaques, we presented peripheral or foveal visual transients during an otherwise stable period of fixation. Such transients resulted in well-known reductions in microsaccade frequency, and our goal was to investigate whether microsaccade kinematics would additionally be altered. We found that both microsaccade timing and amplitude were modulated by the visual transients, and in predictable manners by these transients' timing and geometry. Interestingly, modulations in the peak velocity of the same movements were not proportional to the observed amplitude modulations, suggesting a violation of the well-known "main sequence" relationship between microsaccade amplitude and peak velocity. We hypothesize that visual stimulation during movement preparation affects not only the saccadic "Go" system driving eye movements but also a "Pause" system inhibiting them. If the Pause system happens to be already turned off despite the new visual input, movement kinematics can be altered by the readout of additional visually evoked spikes in the Go system coding for the flash location. Our results demonstrate precise control over individual microscopic saccades and provide testable hypotheses for mechanisms of saccade control in general.

Indexed as

Evoked Potentials, VisualSaccadesAnimalsBiomechanical PhenomenaFixation, OcularMacaca mulattaMaleModels, NeurologicalVisual Perceptionmicrosaccadesomnipause neuronssaccadessaccadic inhibitionsuperior colliculus

Identifiers

PMID28202573
PMCPMC5411461

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.