Literature DB >> 3803492

Human express saccades: effects of randomization and daily practice.

B Fischer, E Ramsperger.   

Abstract

When human subjects are asked to execute saccades from a fixation point to a peripheral target, if the fixation point is turned off some time (200 ms) before the target is turned on, the distribution of the saccadic reaction times is bimodal. The first peak occurs at about 100 ms and represents the population of express saccades. If the target location is kept constant the express saccades have reaction times of about 100 ms. If the target location is randomized between right and left (distance from fixation point constant at 4 deg) the reaction times of the express saccades are increased by about 15 ms. If the target location is randomized between 4 deg and 8 deg (direction constant to the right) no increase of the reaction time is observed. The proportion of express saccades increases with daily practice and their reaction times decrease slightly from 105 ms to 98 ms. If an anticipatory saccade was made after reaction times below 75 ms, it frequently undershot the target by more than 20% and was followed by a corrective saccade. The corrections could be executed at times where usually an express saccade would have occurred such that all of these corrections began at about the same time, i.e. 100 ms after target onset, implying intersaccadic intervals between 100 ms and zero (!)

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Year:  1986        PMID: 3803492     DOI: 10.1007/bf00340494

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  32 in total

1.  Further observations on the occurrence of express-saccades in the monkey.

Authors:  R Boch; B Fischer
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

2.  Corollary discharge provides accurate eye position information to the oculomotor system.

Authors:  B L Guthrie; J D Porter; D L Sparks
Journal:  Science       Date:  1983-09-16       Impact factor: 47.728

3.  Vision during saccadic eye movements. II. A corollary discharge to monkey superior colliculus.

Authors:  B J Richmond; R H Wurtz
Journal:  J Neurophysiol       Date:  1980-04       Impact factor: 2.714

4.  Removing the superior colliculus silences eye movements normally evoked from stimulation of the parietal and occipital eye fields.

Authors:  E G Keating; S G Gooley; S E Pratt; J E Kelsey
Journal:  Brain Res       Date:  1983-06-13       Impact factor: 3.252

5.  Modifications of presaccadic activation on neurons in the extrastriate cortex during prolonged training of rhesus monkeys in a visuo-oculomotor task.

Authors:  B Fischer; R Boch
Journal:  Neurosci Lett       Date:  1982-05-28       Impact factor: 3.046

6.  Selection of visual targets activates prelunate cortical cells in trained rhesus monkey.

Authors:  B Fischer; R Boch
Journal:  Exp Brain Res       Date:  1981       Impact factor: 1.972

7.  Behavioral enhancement of visual responses in monkey cerebral cortex. I. Modulation in posterior parietal cortex related to selective visual attention.

Authors:  M C Bushnell; M E Goldberg; D L Robinson
Journal:  J Neurophysiol       Date:  1981-10       Impact factor: 2.714

8.  Enhanced activation of neurons in prelunate cortex before visually guided saccades of trained rhesus monkeys.

Authors:  B Fischer; R Boch
Journal:  Exp Brain Res       Date:  1981       Impact factor: 1.972

9.  Effects of components of displacement-step stimuli upon latency for saccadic eye movement.

Authors:  M G Saslow
Journal:  J Opt Soc Am       Date:  1967-08

10.  Visual responses of inferior temporal neurons in awake rhesus monkey.

Authors:  B J Richmond; R H Wurtz; T Sato
Journal:  J Neurophysiol       Date:  1983-12       Impact factor: 2.714

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  42 in total

1.  The reduction of saccadic latency by prior offset of the fixation point: an analysis of the gap effect.

Authors:  P A Reuter-Lorenz; H C Hughes; R Fendrich
Journal:  Percept Psychophys       Date:  1991-02

2.  Is the relationship of prosaccade reaction times and antisaccade errors mediated by working memory?

Authors:  Trevor J Crawford; Elisabeth Parker; Ivonne Solis-Trapala; Jenny Mayes
Journal:  Exp Brain Res       Date:  2010-11-25       Impact factor: 1.972

3.  Preparatory activations across a distributed cortical network determine production of express saccades in humans.

Authors:  Jordan P Hamm; Kara A Dyckman; Lauren E Ethridge; Jennifer E McDowell; Brett A Clementz
Journal:  J Neurosci       Date:  2010-05-26       Impact factor: 6.167

4.  Characteristics of "anti" saccades in man.

Authors:  B Fischer; H Weber
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

5.  Behavioral plasticity of antisaccade performance following daily practice.

Authors:  Kara A Dyckman; Jennifer E McDowell
Journal:  Exp Brain Res       Date:  2004-11-13       Impact factor: 1.972

6.  Occurrence of human express saccades depends on stimulus uncertainty and stimulus sequence.

Authors:  M Jüttner; W Wolf
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

7.  Asymmetry of the amplitude-time properties of directed saccades in monkeys depending on the complexity of the spatial scheme of visual stimulation.

Authors:  L V Tereshchenko; S A Molchanov; O V Kolesnikova; A V Latanov; V V Shul'govskii
Journal:  Neurosci Behav Physiol       Date:  2006-10

Review 8.  Fixation-point offsets reduce the latency of saccades to acoustic targets.

Authors:  R Fendrich; H C Hughes; P A Reuter-Lorenz
Journal:  Percept Psychophys       Date:  1991-10

9.  Express saccades: is there a separate population in humans?

Authors:  M G Wenban-Smith; J M Findlay
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

10.  The influence of motor training on human express saccade production.

Authors:  Raquel Bibi; Jay A Edelman
Journal:  J Neurophysiol       Date:  2009-09-23       Impact factor: 2.714

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