Biomedical subjects

A Toet

Publications and source records attributed to A Toet.

3 recordsLinked to original sources

PubMed1992

Visual processing of optic acceleration.

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.

Fixation, Ocular↗

PubMed1992

The two-dimensional shape of spatial interaction zones in the parafovea.

The spatial analysis of a target may be strongly degraded by the simultaneous presentation of nearby pattern elements. The present study investigated the shape and extent of the region of interaction as a function of retinal location. The stimuli consisted of 3 collinear [symbol: see text] s which were randomly oriented up ([symbol: see text]) or down ([symbol: see text]). The task was to discriminate the orientation of the middle [symbol: see text]. The retinal locations studied were at 0, 2.5, 5 and 10 degrees, on the lower vertical meridian and on the nasal halves of both the horizontal and the 45 degrees diagonal visual field meridians. The extent of the interaction region was defined as the separation between the midpoint of two adjacent [symbol: see text] s that resulted in 75% correct discrimination. The shape of the interaction region was determined by using several orientations (horizontal, vertical, left diagonal and right diagonal) for the virtual line joining the 3. [symbol: see text] s. Our results show that the size of the interaction regions varies linearly with eccentricity as does the size of a just resolved individual [symbol: see text]. However, the size of the interaction region varies much more rapidly than does the resolution threshold for an individual [symbol: see text]. The spatial interaction zones appear to be elongated radially, so that they have an elliptical shape. The size of the major axis is about 2-3 times the size of the minor axis. The major axis is along the meridian through the central visual field (i.e. it is oriented radially) while the minor axis is oriented tangentially (i.e. isoeccentrically).

Adult↗

PubMed1991

Spatiotemporal representation of moving luminance edges in human vision.

The edges of straight bars in a square-wave luminance grating appear undulating to an observer when the retinal image of this pattern is in motion. The amplitude of the perceived undulations increases linearly with retinal image speed with an average slope of 30 +/- 4 ms. The period of the motion-induced bulges is 2.5 +/- 0.5 degree and shows no consistent variation with the retinal image velocity of the pattern. The close quantitative agreement between the spatiotemporal extent of this effect and recent estimates of the spatiotemporal parameters of human motion-sensitive mechanisms suggests the existence of motion-sensitive cells in the central nervous system that have a fixed time constant but change the shape and size of their retinal support with retinal image velocity.

Humans↗