This study employed a selective adaptation paradigm and investigated thresholds for direction discrimination of translational stereoscopic motion (moving binocular disparity information). The stimuli were moving arrays of randomly positioned stereoscopic discs created from disparity embedded in dynamic random-element stereograms. When discrimination thresholds were measured across a range of ba...

We have measured how color appearance of square-wave bars varies with stimulus strength and spatial frequency. Observers adjusted the color of a uniform patch to match the color appearance of the bars in square-wave patterns. We used low-to-moderate square-wave patterns, from 1 to 8 cycles per degree (c/deg). The matches are not photoreceptor matches but rather are established at more central n...

Contrast thresholds were measured for discriminating left vs right motion of a vertical, 1 c/deg luminance grating lasting for one cycle of motion. This test was presented on a 1 c/deg stationary grating (pedestal) of twice-threshold, flashed for the duration of the test motion. Lu and Sperling [(1995). Vision Research, 35, 2697-2722] argue that the visual system detects the underlying, first-o...

The hypothesis that oculomotor smooth pursuit (SP) adaptation is accompanied by alterations in velocity perception was tested by assessing coherence thresholds, using random-dot kinematograms before and after the adaptation paradigm. The results showed that the sensitivity to coherent motion at 10 deg/sec (the initial target velocity during adaptation) was reduced after the SP adaptation, endin...

Both chromatic and luminance-modulated stimuli are served by multiple spatial-frequency-tuned channels. This experiment investigated the independence versus interdependence of spatial frequency channels that serve the detection of red-green chromatic versus yellow-black luminance-modulated stimuli at low spatial frequencies. Contrast thresholds for both chromatic and luminance-modulated grating...

Adapting one eye to a high contrast grating reduces sensitivity to similar target gratings shown to the same eye, and also to those shown to the opposite eye. According to the textbook account, interocular transfer (IOT) of adaptation is around 60% of the within-eye effect. However, most previous studies on this were limited to using high spatial frequencies, sustained presentation, and criteri...

An object moving against a textured background is accurately perceived when viewed foveally, but when viewed peripherally the object's perceived direction of motion may deviate from veridical by as much as 90 deg. The illusory direction is oblique to the orientation of the background contours, which may themselves be moving or stationary. In several experiments, we examined the boundary conditi...

We investigated the direction-specificity of motion adaptation, by recording magnetic responses evoked by motion onsets under both adapted and control conditions. The inter-stimulus interval was equated between the conditions to precisely evaluate the effect of motion adaptation itself. The onset stimuli at 1.5, 3.0 or 6.0 deg/s moved in the same direction or in the opposite direction to an ada...

Recent work has revealed multiple pathways for cross-orientation suppression in cat and human vision. In particular, ipsiocular and interocular pathways appear to assert their influence before binocular summation in human but have different (1) spatial tuning, (2) temporal dependencies, and (3) adaptation after-effects. Here we use mask components that fall outside the excitatory passband of th...

We measured stereoscopic slant detection thresholds for surfaces slanting about a horizontal or a vertical axis. For random-dot covered surfaces, 1.25 deg of slant was required to detect slant about a horizontal axis, whereas 2.1 deg of slant was required to detect slant about a vertical axis. This anisotropy could be due to the fact that orientation disparities, which contain information about...