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F Behrens

Publications and source records attributed to F Behrens.

57 records · Page 4Linked to original sources

Investigation of the horizontal, vertical, and oblique optokinetic nystagmus and afternystagmus in squirrel monkeys.

A moving random dot pattern was projected onto a tangent screen in front of awake untrained monkeys that were always placed in upright position. Eye movements were recorded in two dimensions to study the oblique optokinetic nystagmus (OKN) and compare it to the horizontal and vertical OKN. Any direction of pattern movement across the screen could be achieved. The angular velocity of pattern movement was varied between 6 and 180 degrees/s. To display off-horizontal and off-vertical eye movements, the instantaneous direction and velocity of the eye movements were computed from the horizontal and vertical search coil voltages. At pattern velocities below 90 degrees/s, stimulus-direction and direction of the OKN slow phase matched very precisely. Above 90 degrees/s the slow-phase eye movement direction was systematically shifted toward the horizontal except for pure vertical stimulation. The slow-phase eye velocity at off-horizontal stimulation was inconstant, however; stable periods occurred repeatedly that were used to define the gain of OKN. Up to stimulus speeds of about 90 degrees/s the OKN gain did not depend on the direction of stimulation and of OKN. At higher velocities the gain decreased with the increasing angle between stimulus direction and horizontal. Practically no vertical optokinetic afternystagmus (OKAN) could be observed, in either the up or down direction. At the onset of afternystagmus after oblique stimulation the direction of the OKAN slow phase immediately shifted over to the horizontal. The data indicate that the slow-phase direction and gain of oblique OKN with the monkey's head upright can be described by the sum of a horizontal and a vertical velocity vector obtained during stimulation in these cardinal directions.

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On the optokinetic response during step-wise changes in stimulus velocity in squirrel monkeys.

In two awake untrained squirrel monkeys the horizontal optokinetic nystagmus (OKN) was studied. The goal was to quantify the buildup of the slow-phase eye movement velocity during the first two seconds and the eye movements after OKN interruption by a stationary surround. We intended to uncover possible effects of a "charged' velocity storage on eye movements at a stationary surround. Using an optokinetic drum, a paradigm was designed to create sudden changes of the pattern (within 5 ms) between appearing to be stationary or rotating. Velocity steps from zero to 14 to 73 degrees/s and back to zero could be achieved. OKN onset: 201 velocity trajectories were analyzed. The mean latency between the onset of pattern movement and the onset of slow-phase eye movements was 82.8 +/- 16.5 ms. Over a limited period the initial increase in slow-phase velocity could be approximated by a straight line. The slope was on average 103 +/- 67 degrees/s2 and did not show a significant dependency on pattern movement velocity. Eye movement velocity at the end of the linear part increased linearly with drum velocity; the slope was 0.59. After the linear range, the slow-phase velocity increased further but at slower accelerations and usually reached the final gain within the two seconds. The initial linear acceleration component is an open-loop reflex response and we conclude that closing the loop happens when about 60% of the stimulus velocity is reached. OKN-offset: The influence of a fully charged OKN velocity storage mechanism on eye movements after a sudden exposure of a stationary surround was studied in 23 trials. After OKN interruption the velocity decay commenced after an interval of 83.5 +/- 16.6 ms. On average the slope of the consecutive linear velocity decay was -195.4 +/- 83.6 degrees/s2. During 5.8 +/- 0.98 s the OKN still had some impact on the fixating eye movements. We conclude that this time represents the time for velocity storage discharging. An active process seems to control the impact of velocity storage on eye movements.

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The velocity storage mechanism of the optokinetic nystagmus under apparent stimulus movements in squirrel monkeys.

Experiments in two awake untrained squirrel monkeys were performed to study the velocity storage mechanism during fast rise of OKN slow phase velocity. This was done by testing the monkey's capability to perform OKN in response to a stationary-appearing stroboscopically illuminated stripe pattern of a horizontally rotating drum. Nystagmus was initially elicited during constant illumination lasting between 0.6 and 25 s. The periodicity of the stripe pattern was 2.37 degrees. When after the constant light the flash illumination was switched on again, two types of behavior could occur, depending on the length of the constant light interval (CLI): 1) when the CLI was shorter than a threshold value of 6.2 seconds, the OKN ceased under the flash stimulation. Then a "post-OKN" occurred that increased with the length of the CLIs, indicating that the intermittently illuminated pattern did not provoke fixation suppression of OKN aftereffects. 2) when the CLI was above threshold, the OKN continued under the flash light; it will be called "apparent movement OKN." The threshold CLI between the type 1 and the type 2 response did not depend on drum velocities between 21.5 degrees/s and 71.3 degrees/s. The average gain of the apparent movement OKN was 0.83 +/- 0.04; gain and stability of slow phase eye movement velocity did not deviate systematically from the usually elicited OKN. OKAN after apparent movement OKN did not deviate from OKAN after constantly illuminated moving patterns. In response to the OKN initiation by a constantly illuminated pattern up to pattern velocities of 100 degrees/s, the OKN steady state gain was reached within the first 2 or 3 nystagmus beats. We ascribe the increase of the post-OKN with CLI and the existence of a threshold constant light interval to activity-accumulation in the common velocity-to-position integrator (velocity storage) of the brain stem. Loading of the velocity storage takes place after the OKN gain has already reached the steady-state value. Apparent movement OKN could also be elicited in guinea pigs that lack an effective smooth pursuit system. We suggest that apparent movement OKN is produced by mechanisms located in the brain stem.

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