Transfer of information from manual to oculomotor control system.

1972 ◽  
Vol 96 (1) ◽  
pp. 92-96 ◽  
Author(s):  
Ronald W. Angel ◽  
Harry Garland
1976 ◽  
Vol 30 (3-4) ◽  
pp. 341-352 ◽  
Author(s):  
B.Yeshwant Kamath ◽  
Edward L. Keller

1988 ◽  
Vol 40 (2) ◽  
pp. 299-322 ◽  
Author(s):  
Nicholas C. Barrett ◽  
Denis J. Glencross

The present paper examines the control principles underlying rapid manual tracking responses to horizontal double-step stimuli. The paper reports an experiment concerned with responses made to step-stimuli presented in quick succession. The amplitude of the second-step was varied between the initial step-position and the home-base. Double-step response parameters were analysed as a function of the determinant time interval (D) between the second step and the onset of the initial response. The initial response amplitude was observed to vary as a function of D. Amplitude transition functions were constructed representing the transition of the initial response amplitude between the two step positions; their slopes, furthermore, depended on the amplitude of the second target step. No delays in the initial reaction time with the interstimulus interval were observed. Minor delays to the onset of a corrective response were observed. These delays were in part related to a movement time constraint that is independent of any limitations in central processing capacity. The present findings for the manual control system are compared to double-step tracking analyses of the oculomotor control system.


1978 ◽  
Vol 23 (s1) ◽  
pp. 286-287
Author(s):  
R. Schmid ◽  
R. Lombardi ◽  
D. Zambarbieri ◽  
A. Buizza

2004 ◽  
Vol 16 (2) ◽  
pp. 318-330 ◽  
Author(s):  
Timothy Lewis Hodgson ◽  
Charlotte Golding ◽  
Dimitra Molyva ◽  
Clive R. Rosenthal ◽  
Christopher Kennard

Active vision is a dynamic process involving the flexible coordination of different gaze strategies to achieve behavioral goals. Although many complex behaviors rely on an ability to efficiently switch between gaze-control strategies, few studies to date have examined mechanisms of task level oculomotor control in detail. Here, we report five experiments in which subjects alternated between conflicting stimulus-saccade mappings within a block of trials. The first experiment showed that there is no performance cost associated with switching between pro and anti saccades. However, follow-up experiments demonstrate that whenever subjects alternate between arbitrary stimulus-saccade mappings, latency costs are apparent on the first trial after a task change. More detailed analysis of switch costs showed that latencies were particularly elevated for saccades directed toward the same location that had been the target for a saccade on the preceeding trial. This saccade “inhibition of return” effect was most marked when unexpected error feedbacks cued task switches, suggesting that saccade selection processes are modulated by reward. We conclude that there are two systems for saccade control that differ in their characteristics following a task switch. The “reflexive” control system can be enabled/disabled in advance of saccade execution without incurring any performance cost. Switch costs are only observed when two or more arbitrary stimulus-saccade mappings have to be coordinated by a “symbolic” control system.


Author(s):  
Marian Szczodrowski

Every human activity, including linguistic and non-linguistic communication among people, is always connected with a type of control appropriate to that activity. In an informationalcommunicative system there functions a parallel control system, which ensures the optimum transfer of information to the receiver or receivers. The following article deals with the essence of the process of control, its course on the inter-individual and intra-individual level of communication between partners, and types of control and their possible effects.


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