PubMed · 6869474
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R W Lingua, S Azen. 1983. Succinyldicholine and the basic ocular deviation.. https://doi.org/10.1016/0002-9394(83)90478-6
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Four experiments are reported in which the subjects had to respond to a target that masked a preceding prime via metacontrast masking. In one part of Experiment 1, the subjects discriminated the target's shape (square or diamond) by a motor-choice reaction, and in another part they had to respond with a simple reaction. The prime was neutral (circular) with respect to the target's shape. The data showed a facilitation effect. In both tasks the reaction time was reduced by the masked prime. However, the reduction was more pronounced with simple reaction than with choice reaction. In the other experiments, additional primes were used with the same angular shapes as the targets. In Experiments 2 and 3, after discriminating the target's shape by a choice reaction, the subjects had to judge the prime's shape in a signal-detection task. While neither the d' value for discriminating the angular primes from the circular ones (Exp. 2) nor the d' value for distinguishing between the angular primes (Exp. 3) was different from zero, the choice-reaction data showed a congruency effect. With a congruent prime (i.e., a prime that had the same shape as the target), the reaction times were reduced. With an incongruent prime, the reaction times grew. In Experiment 4 the errors were investigated. The facilitation effect was present in the RT, but not in the number of errors, whereas the congruency effect was present in the number, but not in the RT of errors. While the facilitation effect can be attributed either to an unspecific activation by the masked prime or to an influence of the prime on attentional processes, the congruency effect can be explained by the assumption that the masked prime directly activates the specific response, which corresponds to the prime's shape.
Congenital nystagmus (CN) has been described as a 'fixation' nystagmus implying an inability to fixate a target. However, each cycle of CN contains a target-foveation period during which the eye velocity is at, or near, zero. Prolongation of foveation time, reduction of retinal image velocity and cycle-to-cycle foveation repeatability all contribute to increased visual acuity. We developed several methods to accurately measure the dynamics of foveation in CN; their use is illustrated on an individual with typical idiopathic CN and no afferent defects. During eight 5-second intervals of fixation on a stationary target, the horizontal standard deviation (SD) of the mean foveation position (FPOS) was 12.82 minarc and the SD of foveation velocity was 118.36 minarc/sec. The SD of the means of total eye position and of the non-foveating peak of the CN were 43.17 and 25.32 minarc respectively. The mean foveation-time interval (eye velocity less than or equal to 4 degrees/sec) was 57.27 msec. The SD FPOS for the best 1-second interval (4 successive CN cycles), in a typical 5-second record, was 0.71 minarc. Histograms revealed peaks of eye position at 0 +/- 10 minarc and of eye velocity at 0 +/- 240 minarc/sec. The small vertical component of the CN (16 minarc peak-to-peak) had a SD of 6.56 minarc. A nystagmus foveation function related to visual acuity was derived that was more sensitive than CN intensity. The increased visual acuity resulting from the use of convergence or base-out prisms was due to increased foveation time. Although it might appear that CN is a defect of fixation, this individual with CN had strong fixation reflexes in the sense that he was able to accurately (within 1 minarc) achieve (interbeat) and maintain (intrabeat) target foveation for appreciable periods of time. Our data support the hypothesis that individuals with idiopathic CN do not have a primary disturbance of fixation.
We present data on the human sensitivity to optic acceleration, i.e. temporal modulations of the speed and direction of moving objects. Modulation thresholds are measured as a function of modulation frequency and speed for different periodical velocity vector modulation functions using a localized target. Evidence is presented that human detection of velocity vector modulations is not directly based on the acceleration signal (the temporal derivative of the velocity vector modulation). Instead, modulation detection is accurately described by a two-stage model: a low-pass temporal filter transformation of the true velocity vector modulation followed by a variance detection stage. A functional description of the first stage is a second order low-pass temporal filter having a characteristic time constant of 40 msec. In effect, the temporal low-pass filter is an integration of the velocity vector modulation within a temporal window of 100-140 msec. A non-trivial link of this low-pass filter stage to the temporal characteristics of standard motion detection mechanisms will be discussed. Velocity vector modulations are detected in the second-stage, whenever the variance of the filtered velocity vector exceeds a certain threshold variance in either the speed or direction dimension. The threshold standard deviations for this variance detection stage are estimated to be 17% for speed modulations and 9% for motion direction modulations.