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Separate populations of visually guided saccades in humans: reaction times and amplitudes

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Summary

The saccadic eye movements of 20 naive adults, 7 naive teenagers, 12 naive children, and 4 trained adult subjects were measured using two single target saccade tasks; the gap and the overlap task. In the gap task, the fixation point was switched off before the target occurred; in the overlap task it remained on until the end of each trial. The target position was randomly selected 4° to the left or 4° to the right of the fixation point. The subjects were instructed to look at the target when it appeared, not to react as fast as possible. They were not given any feedback about their performance. The results suggest that, in the gap task, most of the naive subjects exhibit at least two (the teenagers certainly three) clearly separated peaks in the distribution of the saccadic reaction times. The first peak occurs between 100 and 135 ms (express saccades), the second one between 140 and 180 ms (fast regular), and a third peak may follow at about 200 ms (slow regular). Other subjects did not show clear signs of two modes in the range of 100 to 180 ms, and still others did not produce any reaction times below 135 ms. In the overlap task as well three or even more peaks were obtained at about the same positions along the reaction time scale of many, but not all subjects. Group data as well as those of individual subjects were fitted by the superposition of three gaussian functions. Segregating the reaction time data into saccades that over- or undershoot the target indicated that express saccades almost never overshoot. The results are discussed in relation to the different neural processes preceding the initiation of visually-guided saccades.

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References

  • Albano JE, King WM (1989) Rapid adaptation of saccadic amplitude in humans and monkeys. Invest Ophthalmol Vis Sci 30: 1883–1893

    Google Scholar 

  • Boch R (1988) Chemical lesions in V1, V2 and V3 of the rhesus monkey: effects upon express-saccades. In: Elsner N, Barth F (eds) Proceedings of the 16th Göttingen Neurobiology Conference. Thieme, Stuttgart, New York

    Google Scholar 

  • Boch R, Fischer B (1986) Further observations on the occurrence of express-saccades in the monkey. Exp Brain Res 63: 487–494

    Google Scholar 

  • Braun D, Breitmeyer BG (1988) Relationship between directed visual attention and saccadic reaction times. Exp Brain Res 73: 546–552

    Google Scholar 

  • Braun D, Breitmeyer BG (1990) Effects of reappearance of fixated and attended stimuli upon saccadic reaction time. Exp Brain Res 81: 318–324

    Google Scholar 

  • Braun D, Weber H, Mergner T, Schulte-Mönting J (1992) Saccadic reaction times in patients with frontal and parietal lesions. Brain (in press)

  • Deubel H, Wolf W, Hauske G (1986) Adaptive gain control of saccadic eye movements. Hum Neurobiol 5: 245–253

    Google Scholar 

  • Findlay JM (1981) Spatial and temporal factors in the predictive generation of saccadic eye movements. Vision Res 21: 347–354

    Google Scholar 

  • Findlay JM (1982) Global visual processing for saccadic eye movements. Vision Res 22: 1033–1045

    Google Scholar 

  • Fischer B (1987) The preparation of visually guided saccades. Rev Physiol Biochem Pharmacol 106: 1–35

    Google Scholar 

  • Fischer B, Boch R (1983) Saccadic eye movements after extremely short reaction times in the monkey. Brain Res 260: 21–26

    Google Scholar 

  • Fischer B, Ramsperger E (1984) Human express saccades: extremely short reaction times of goal directed eye movements. Exp Brain Res 57: 191–195

    Google Scholar 

  • Fischer B, Ramsperger E (1986) Human express saccades: effects of randomization and daily practice. Exp Brain Res 64: 569–578

    Google Scholar 

  • Fischer B, Weber H (1990) Saccadic reaction times of dyslexic and age-matched normal subjects. Perception 19: 805–818

    Google Scholar 

  • Fischer B, Boch R, Ramsperger E (1984) Express-saccades of the monkey: effect of daily training on probability of occurrence and reaction time. Exp Brain Res 55: 232–242

    Google Scholar 

  • Gauthier G, Volle M (1975) Two dimensional eye movement monitor for clinical laboratory recordings. Electroencephalogr Clin Neurophysiol 39: 285–291

    Google Scholar 

  • Guitton D, Buchtel HA, Douglas RM (1985) Frontal lobe lesions in man cause difficulties in suppressing reflexive glances and in generating goal-directed saccades. Exp Brain Res 58: 455–472

    Google Scholar 

  • Jüttner M, Wolf W (1991) Human express saccades: catch trials influence the probability of their occurrence. In: Schmidt R, Zambarbieri D (eds) Oculomotor control and cognitive processes. North Holland, Amsterdam, pp 163–178

    Google Scholar 

  • Kalesnykas RP, Hallett PE (1987) The differentiation of visually guided and anticipatory saccades in gap and overlap paradigms. Exp Brain Res 68: 115–121

    Google Scholar 

  • Kapoula Z (1985) Evidence for a range effect in the saccadic system. Vision Res 25: 1155–1157

    Google Scholar 

  • Mayfrank L, Mobashery M, Kimmig H, Fischer B (1986) The role of fixation and visual attention in the occurrence of express saccades in man. Eur Arch Psychiat Neurol Sci 235: 269–275

    Google Scholar 

  • Mergner T, Evdokimidis I, Lucking C (1991) Cortical potentials preceding different types of saccadic eye movements. In: van Rensbergen J, Devijver M, d'Ydevalle G (eds) Proceedings of the Sixth European Conference on Eye Movements, Leuven, pp 45–46

  • Munoz D, Wurtz R (1991) Disruption of visual fixation following injection of GABAergic drugs into the fixation zone of the primate superior colliculus. Soc Neurosci Abstr 17: 544, No. 218.4

    Google Scholar 

  • Parlitz D, Nothdurft C (1990) Does pop-out of orientation or motion produce express saccades? In: Elsner N, Roth G (eds) Brain — perception — cognition. Thieme, Stuttgart, New York, p 258

    Google Scholar 

  • Reuter-Lorenz P, Hughes H, Fendrich R (1991) The reduction of saccadic latency by prior offset of the fixation point: an analysis of the gap effect. Percept Psychophys 49: 167–175

    Google Scholar 

  • Saslow MG (1967) Effects of components of displacement-step stimuli upon latency for saccadic eye movement. J Opt Soc Am 57: 1024–1029

    CAS  PubMed  Google Scholar 

  • Schiller PH, Sandell JH, Maunsell JH (1987) The effect of frontal eye field and superior colliculus lesions on saccadic latencies in the rhesus monkey. J Neurophysiol 57: 1033–1049

    Google Scholar 

  • Smit AC, van Gisbergen JA (1989) A short-latency transition in saccade dynamics during square-wave tracking and its significance for the differentiation of visually guided and predictive saccades. Exp Brain Res 76: 64–74

    CAS  PubMed  Google Scholar 

  • Weber H, Fischer B (1990) Effect of a local ibotenic acid lesion in the visual association area on the prelunate gyrus (area V4) on saccadic reaction times in trained rhesus monkeys. Exp Brain Res 81: 134–139

    Google Scholar 

  • Weber H, Latanov A, Fischer B (1992) Context dependent amplitude modulations of express and regular saccades in man and monkey. Exp Brain Res (in press)

  • Wenban-Smith M, Findlay J (1991) Express-saccades: is there a separate population in humans? Exp Brain Res 87: 218–222

    Google Scholar 

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Fischer, B., Weber, H., Biscaldi, M. et al. Separate populations of visually guided saccades in humans: reaction times and amplitudes. Exp Brain Res 92, 528–541 (1993). https://doi.org/10.1007/BF00229043

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