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Decisions in motion: vestibular contributions to saccadic target selection

Authors :
K. Halfwerk
Luc P. J. Selen
W.P. Medendorp
Mathieu Koppen
L. Rincon-Gonzalez
Brian D. Corneil
Source :
Journal of Neurophysiology, 116, 977-985, Brain and Mind Institute Researchers' Publications, Journal of Neurophysiology, 116, 3, pp. 977-985
Publication Year :
2016
Publisher :
American Physiological Society, 2016.

Abstract

Contains fulltext : 159350.pdf (Publisher’s version ) (Closed access) The natural world continuously presents us with many opportunities for action, thus a process of target selection must precede action execution. While there has been considerable progress in understanding target selection in stationary environments, little is known about target selection when we are in motion. Here we investigated the effect of self-motion signals on saccadic target selection in a dynamic environment. Human subjects were sinusoidally translated (f=0.6 Hz, 30 cm peak-to-peak displacement) along an inter-aural axis using a vestibular sled. During the motion two visual targets were presented asynchronously but equidistantly on either side of fixation. Subjects had to look at one of these targets as quickly as possible. Using an adaptive approach, the time delay between these targets was adjusted until the subject selected both targets equally often. We determined this balanced time delay for different phases of the motion in order to distinguish the effects of body acceleration and velocity on saccadic target selection. Results show that acceleration (or position, as these are indistinguishable during sinusoidal motion), but not velocity, affect target selection for saccades. Subjects preferred to look at targets in the direction of the acceleration - the leftward target was preferred when the sled accelerated to the left, and vice versa. Saccadic reaction times mimicked this selection bias by being reliably shorter to targets in the direction of acceleration. Our results provide evidence that saccade target selection mechanisms are modulated by self-motion signals, which could be derived directly from the otolith system. 9 p.

Details

ISSN :
15221598 and 00223077
Volume :
116
Database :
OpenAIRE
Journal :
Journal of Neurophysiology
Accession number :
edsair.doi.dedup.....fabfdb2ab123f2a93279cd45161923f3