Modeling Multisensory Processes in Saccadic Responses

Author(s):  
Adele Diederich ◽  
Hans Colonius
2019 ◽  
Vol 121 (5) ◽  
pp. 1588-1590 ◽  
Author(s):  
Luca Casartelli

Neural, oscillatory, and computational counterparts of multisensory processing remain a crucial challenge for neuroscientists. Converging evidence underlines a certain efficiency in balancing stability and flexibility of sensory sampling, supporting the general idea that multiple parallel and hierarchically organized processing stages in the brain contribute to our understanding of the (sensory/perceptual) world. Intriguingly, how temporal dynamics impact and modulate multisensory processes in our brain can be investigated benefiting from studies on perceptual illusions.


2021 ◽  
Vol 7 (12) ◽  
pp. eabf4355
Author(s):  
Patrick G. Bissett ◽  
Henry M. Jones ◽  
Russell A. Poldrack ◽  
Gordon D. Logan

The stop-signal paradigm, a primary experimental paradigm for understanding cognitive control and response inhibition, rests upon the theoretical foundation of race models, which assume that a go process races independently against a stop process that occurs after a stop-signal delay (SSD). We show that severe violations of this independence assumption at short SSDs occur systematically across a wide range of conditions, including fast and slow reaction times, auditory and visual stop signals, manual and saccadic responses, and especially in selective stopping. We also reanalyze existing data and show that conclusions can change when short SSDs are excluded. Last, we suggest experimental and analysis techniques to address this violation, and propose adjustments to extant models to accommodate this finding.


Perception ◽  
10.1068/p7085 ◽  
2012 ◽  
Vol 41 (2) ◽  
pp. 131-147 ◽  
Author(s):  
Nicola J Gregory ◽  
Timothy L Hodgson

Pointing with the eyes or the finger occurs frequently in social interaction to indicate direction of attention and one's intentions. Research with a voluntary saccade task (where saccade direction is instructed by the colour of a fixation point) suggested that gaze cues automatically activate the oculomotor system, but non-biological cues, like arrows, do not. However, other work has failed to support the claim that gaze cues are special. In the current research we introduced biological and non-biological cues into the anti-saccade task, using a range of stimulus onset asynchronies (SOAs). The anti-saccade task recruits both top–down and bottom–up attentional mechanisms, as occurs in naturalistic saccadic behaviour. In experiment 1 gaze, but not arrows, facilitated saccadic reaction times (SRTs) in the opposite direction to the cues over all SOAs, whereas in experiment 2 directional word cues had no effect on saccades. In experiment 3 finger pointing cues caused reduced SRTs in the opposite direction to the cues at short SOAs. These findings suggest that biological cues automatically recruit the oculomotor system whereas non-biological cues do not. Furthermore, the anti-saccade task set appears to facilitate saccadic responses in the opposite direction to the cues.


2013 ◽  
Vol 109 (2) ◽  
pp. 518-545 ◽  
Author(s):  
K. P. Schultz ◽  
C. Busettini

Saccadic eye movements are rapid transfers of gaze between objects of interest. Their duration is too short for the visual system to be able to follow their progress in time. Adaptive mechanisms constantly recalibrate the saccadic responses by detecting how close the landings are to the selected targets. The double-step saccadic paradigm is a common method to simulate alterations in saccadic gain. While the subject is responding to a first target shift, a second shift is introduced in the middle of this movement, which masks it from visual detection. The error in landing introduced by the second shift is interpreted by the brain as an error in the programming of the initial response, with gradual gain changes aimed at compensating the apparent sensorimotor mismatch. A second shift applied dichoptically to only one eye introduces disconjugate landing errors between the two eyes. A monocular adaptive system would independently modify only the gain of the eye exposed to the second shift in order to reestablish binocular alignment. Our results support a binocular mechanism. A version-based saccadic adaptive process detects postsaccadic version errors and generates compensatory conjugate gain alterations. A vergence-based saccadic adaptive process detects postsaccadic disparity errors and generates corrective nonvisual disparity signals that are sent to the vergence system to regain binocularity. This results in striking dynamical similarities between visually driven combined saccade-vergence gaze transfers, where the disparity is given by the visual targets, and the double-step adaptive disconjugate responses, where an adaptive disparity signal is generated internally by the saccadic system.


1982 ◽  
Vol 47 (3) ◽  
Author(s):  
D. Zambarbieri ◽  
R. Schmid ◽  
G. Magenes ◽  
C. Prablanc
Keyword(s):  

Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 47-47 ◽  
Author(s):  
J M Findlay ◽  
R Walker ◽  
V Brown ◽  
I Gilchrist ◽  
M Clarke

Individuals with strabismus frequently show a suppression phenomenon in which part of the visual input in one eye is apparently ignored when both eyes are seeing, although the eye may have normal vision when used monocularly. This is often described as an adaptive response to avoid diplopia. We have examined two patients with microstrabismus (angle of squint less than 5 deg) who show strong suppression but with only mild amblyopia. We studied saccade generation in the two eyes using a red — green anaglyph display which allowed us to present stimuli independently to each eye. When single targets were presented in the suppressing eye, saccadic responses usually occurred. However the latencies of these saccades were increased with respect to those elicited from the normal eye (by about 70 ms for one subject and 270 ms for the other). The amplitudes of the saccades were less consistent than those of the normal eye, and saccades were sometimes made in the opposite direction to the target. We also investigated the remote distractor effect. This effect is found consistently in normal subjects and consists of an increase in the latency of a target-elicited saccade when a distractor is simultaneously presented elsewhere in the visual field. When distractors were presented in the suppressing eye, they had no effect on the latency of saccades to a simultaneous target in the other eye. We conclude that visual stimulation in a suppressing eye has no rapid access to the saccadic system.


1999 ◽  
Vol 105 (2) ◽  
pp. 1391-1392
Author(s):  
Heike Heuermann‐Mehmood ◽  
Hans Colonius
Keyword(s):  

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