Literature DB >> 26311763

Does the Brain Extrapolate the Position of a Transient Moving Target?

Julie Quinet1, Laurent Goffart2.   

Abstract

When an object moves in the visual field, its motion evokes a streak of activity on the retina and the incoming retinal signals lead to robust oculomotor commands because corrections are observed if the trajectory of the interceptive saccade is perturbed by a microstimulation in the superior colliculus. The present study complements a previous perturbation study by investigating, in the head-restrained monkey, the generation of saccades toward a transient moving target (100-200 ms). We tested whether the saccades land on the average of antecedent target positions or beyond the location where the target disappeared. Using target motions with different speed profiles, we also examined the sensitivity of the process that converts time-varying retinal signals into saccadic oculomotor commands. The results show that, for identical overall target displacements on the visual display, saccades toward a faster target land beyond the endpoint of saccades toward a target moving slower. The rate of change in speed matters in the visuomotor transformation. Indeed, in response to identical overall target displacements and durations, the saccades have smaller amplitude when they are made in response to an accelerating target than to a decelerating one. Moreover, the motion-related signals have different weights depending upon their timing relative to the target onset: early signals are more influential in the specification of saccade amplitude than later signals. We discuss the "predictive" properties of the visuo-saccadic system and the nature of this location where the saccades land, after providing some critical comments to the "hic-et-nunc" hypothesis (Fleuriet and Goffart, 2012). SIGNIFICANCE STATEMENT: Complementing the work of Fleuriet and Goffart (2012), this study is a contribution to the more general scientific research aimed at understanding how ongoing action is dynamically and adaptively adjusted to the current spatiotemporal aspects of its goal. Using the saccadic eye movement as a probe, we provide results that are critical for investigating and understanding the neural basis of motion extrapolation and prediction.
Copyright © 2015 the authors 0270-6474/15/3511780-11$15.00/0.

Entities:  

Keywords:  adaptation; extrapolation; interception; prediction; saccade; visual motion

Mesh:

Year:  2015        PMID: 26311763      PMCID: PMC6705453          DOI: 10.1523/JNEUROSCI.1212-15.2015

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  42 in total

1.  Comparison of saccades perturbed by stimulation of the rostral superior colliculus, the caudal superior colliculus, and the omnipause neuron region.

Authors:  N J Gandhi; E L Keller
Journal:  J Neurophysiol       Date:  1999-12       Impact factor: 2.714

2.  Blink-perturbed saccades in monkey. I. Behavioral analysis.

Authors:  H H Goossens; A J Van Opstal
Journal:  J Neurophysiol       Date:  2000-06       Impact factor: 2.714

3.  Concurrent processing of saccades in visual search.

Authors:  R M McPeek; A A Skavenski; K Nakayama
Journal:  Vision Res       Date:  2000       Impact factor: 1.886

4.  Predictive elements in ocular interception and tracking of a moving target by untrained cats.

Authors:  F Klam; J Petit; A Grantyn; A Berthoz
Journal:  Exp Brain Res       Date:  2001-07       Impact factor: 1.972

5.  The representation of the visual field on the cerebral cortex in monkeys.

Authors:  P M DANIEL; D WHITTERIDGE
Journal:  J Physiol       Date:  1961-12       Impact factor: 5.182

Review 6.  The characteristics and neuronal substrate of saccadic eye movement plasticity.

Authors:  J Johanna Hopp; Albert F Fuchs
Journal:  Prog Neurobiol       Date:  2004-01       Impact factor: 11.685

7.  The relationship between saccadic and smooth tracking eye movements.

Authors:  C RASHBASS
Journal:  J Physiol       Date:  1961-12       Impact factor: 5.182

8.  Short-term priming, concurrent processing, and saccade curvature during a target selection task in the monkey.

Authors:  R M McPeek; E L Keller
Journal:  Vision Res       Date:  2001-03       Impact factor: 1.886

9.  Involvement of the cerebellar thalamus in human saccade adaptation.

Authors:  B Gaymard; S Rivaud-Péchoux; J Yelnik; B Pidoux; C J Ploner
Journal:  Eur J Neurosci       Date:  2001-08       Impact factor: 3.386

10.  What triggers catch-up saccades during visual tracking?

Authors:  Sophie de Brouwer; Demet Yuksel; Gunnar Blohm; Marcus Missal; Philippe Lefèvre
Journal:  J Neurophysiol       Date:  2002-03       Impact factor: 2.714

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  9 in total

Review 1.  Neurophysiology of visually guided eye movements: critical review and alternative viewpoint.

Authors:  Laurent Goffart; Clara Bourrelly; Jean-Charles Quinton
Journal:  J Neurophysiol       Date:  2018-10-31       Impact factor: 2.714

2.  Motion Extrapolation for Eye Movements Predicts Perceived Motion-Induced Position Shifts.

Authors:  Elle van Heusden; Martin Rolfs; Patrick Cavanagh; Hinze Hogendoorn
Journal:  J Neurosci       Date:  2018-08-13       Impact factor: 6.167

3.  Learning the trajectory of a moving visual target and evolution of its tracking in the monkey.

Authors:  Clara Bourrelly; Julie Quinet; Patrick Cavanagh; Laurent Goffart
Journal:  J Neurophysiol       Date:  2016-09-28       Impact factor: 2.714

4.  The superior colliculus and the steering of saccades toward a moving visual target.

Authors:  Laurent Goffart; Aaron L Cecala; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2017-09-13       Impact factor: 2.714

5.  The caudal fastigial nucleus and the steering of saccades toward a moving visual target.

Authors:  Clara Bourrelly; Julie Quinet; Laurent Goffart
Journal:  J Neurophysiol       Date:  2018-04-11       Impact factor: 2.714

6.  Pursuit disorder and saccade dysmetria after caudal fastigial inactivation in the monkey.

Authors:  Clara Bourrelly; Julie Quinet; Laurent Goffart
Journal:  J Neurophysiol       Date:  2018-07-11       Impact factor: 2.714

7.  Decoding Target Distance and Saccade Amplitude from Population Activity in the Macaque Lateral Intraparietal Area (LIP).

Authors:  Frank Bremmer; Andre Kaminiarz; Steffen Klingenhoefer; Jan Churan
Journal:  Front Integr Neurosci       Date:  2016-08-31

Review 8.  Predictive Coding with Neural Transmission Delays: A Real-Time Temporal Alignment Hypothesis.

Authors:  Hinze Hogendoorn; Anthony N Burkitt
Journal:  eNeuro       Date:  2019-05-07

9.  Coding of interceptive saccades in parietal cortex of macaque monkeys.

Authors:  Jan Churan; Andre Kaminiarz; Jakob C B Schwenk; Frank Bremmer
Journal:  Brain Struct Funct       Date:  2021-09-01       Impact factor: 3.270

  9 in total

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