A Control Systems Model of Smooth Pursuit Eye Movements with Realistic Emergent Properties

1989 ◽  
Vol 1 (1) ◽  
pp. 116-122 ◽  
Author(s):  
R. J. Krauzlis ◽  
S. G. Lisberger

Visual tracking of objects in a noisy environment is a difficult problem that has been solved by the primate oculomotor system, but remains unsolved in robotics. In primates, smooth pursuit eye movements match eye motion to target motion to keep the eye pointed at smoothly moving targets. We have used computer models as a tool to investigate possible computational strategies underlying this behavior. Here, we present a model based upon behavioral data from monkeys. The model emphasizes the variety of visual signals available for pursuit and, in particular, includes a sensitivity to the acceleration of retinal images. The model was designed to replicate the initial eye velocity response observed during pursuit of different target motions. The strength of the model is that it also exhibits a number of emergent properties that are seen in the behavior of both humans and monkeys. This suggests that the elements in the model capture important aspects of the mechanism of visual tracking by the primate smooth pursuit system.

2003 ◽  
Vol 90 (3) ◽  
pp. 1489-1502 ◽  
Author(s):  
Uwe J. Ilg ◽  
Peter Thier

Because smooth-pursuit eye movements (SPEM) can be executed only in the presence of a moving target, it has been difficult to attribute the neuronal activity observed during the execution of these eye movements to either sensory processing or to motor preparation or execution. Previously, we showed that rhesus monkeys can be trained to perform SPEM directed toward an “imaginary” target defined by visual cues confined to the periphery of the visual field. The pursuit of an “imaginary” target provides the opportunity to elicit SPEM without stimulating visual receptive fields confined to the center of the visual field. Here, we report that a subset of neurons [85 “ imaginary” visual tracking (iVT)-neurons] in area MST of 3 rhesus monkeys were identically activated during pursuit of a conventional, foveal dot target and the “imaginary” target. Because iVT-neurons did not respond to the presentation of a moving “imaginary” target during fixation of a stationary dot, we are able to exclude that responses to pursuit of the “imaginary” target were artifacts of stimulation of the visual field periphery. Neurons recorded from the representation of the central parts of the visual field in neighboring area MT, usually vigorously discharging during pursuit of foveal targets, in no case responded to pursuit of the “imaginary” target. This dissociation between MT and MST neurons supports the view that pursuit responses of MT neurons are the result of target image motion, whereas those of iVT-neurons in area MST reflect an eye movement–related signal that is nonretinal in origin. iVT-neurons fell into two groups, depending on the properties of the eye movement–related signal. Whereas most of them (71%) encoded eye velocity, a minority showed responses determined by eye position, irrespective of whether eye position was changed by smooth pursuit or by saccades. Only the former group exhibited responses that led the eye movement, which is a prerequisite for a causal role in the generation of SPEM.


2011 ◽  
Vol 70 ◽  
pp. 352-352 ◽  
Author(s):  
K Strand Brodd ◽  
K Rosander ◽  
H Grönqvist ◽  
G Holmström ◽  
B Strömberg ◽  
...  

1983 ◽  
Vol 79 (2-3) ◽  
pp. 190-192 ◽  
Author(s):  
G. Tedeschi ◽  
P. R. M. Bittencourt ◽  
A. T. Smith ◽  
A. Richens

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