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Biomedical subjects

Erich W Graf

Publications and source records attributed to Erich W Graf.

7 recordsLinked to original sources

Experience can change the 'light-from-above' prior.

To interpret complex and ambiguous input, the human visual system uses prior knowledge or assumptions about the world. We show that the 'light-from-above' prior, used to extract information about shape from shading is modified in response to active experience with the scene. The resultant adaptation is not specific to the learned scene but generalizes to a different task, demonstrating that priors are constantly adapted by interactive experience with the environment.

Adaptation, Physiological↗

Prior depth information can bias motion perception.

Previous studies of the motion aperture problem have shown that the direction of grating motion can be biased by using binocular disparity to designate borders of the aperture as intrinsic (belonging to the grating) or extrinsic (resulting from occlusion of the grating). Observers report motion in the direction of the extrinsic border, as if the grating was extended and moving underneath an occluding surface. Here we investigate whether prior information about depth ordering, given by structure-from-motion, can bias the perceived motion direction of a subsequent moving grating in a similar manner. We presented an aperture stimulus that rotated about its vertical and horizontal axes, revealing the depth relationships (intrinsic and extrinsic) of the aperture borders. The grating then translated within the aperture and observers reported the direction of perceived motion. The test stimulus contained no information about the depth ordering of the scene. We found that observers' reported motion shifted toward the direction of the occluding edges, consistent with the intrinsic-extrinsic border predictions. These results indicate that prior scene information, not just depth information explicitly defined in the test stimulus, is used to help solve the motion aperture problem.

Bias↗

Spatial and temporal tuning of motion in depth.

We used the Pulfrich effect to investigate perception of motion in depth. Independent manipulation of spatial and temporal frequency content in stereoscopic motion stimuli revealed the tuning characteristics of motion-in-depth perception. Sensitivity to interocular phase difference between sinusoidally oscillating sine-wave gratings was measured in four observers who judged direction of motion in depth. Discrimination thresholds in terms of interocular phase difference were determined to investigate spatial and temporal tuning characteristics of a system that is based on interocular phase difference, interocular delay, binocular disparity and velocity difference. Temporal frequency tuning of interocular phase difference thresholds was band pass and relatively dependent on spatial frequency variation. These results together with evidence from two control experiments support the idea that sensitivity to direction of motion in depth is limited by a stereo-motion system that monitors binocular horizontal disparity and motion rather than interocular phase difference, interocular delay, or interocular velocity difference.

Computer Simulation↗

Comparison of the time courses of concomitant and nonconcomitant vertical phoria adaptation.

Vertical phoria adaptation was measured before, during, and after 1 h of training with either a prism or magnifying lens. With the prism (concomitant adaptation) a single vertical disparity was presented at primary position. With the magnifier (nonconcomitant adaptation) two vertical disparities of opposite sign were presented along the vertical meridian. Following adaptation, binocular vision was prevented with an eye patch, and vertical phorias were measured periodically along the primary vertical meridian over the course of 8 h. Despite individual variation, adaptation followed approximately exponential time courses. The average time constants for the decay of concomitant and nonconcomitant adaptation were 31 and 83 min, respectively. There was no consistent relationship between the rates of acquisition and decay nor was there a strong relationship between the gains of the adaptive responses and the rates of decay although there was a general trend for the gains of the nonconcomitant responses to be higher and the rate of decay slower than the concomitant responses. The results support the notion that concomitant and nonconcomitant phoria adaptation involve different mechanisms but not the contention that adaptation to prisms is easier or more robust than adaptation to lenses.

Adaptation, Physiological↗

Changes in cyclotorsion and vertical eye alignment during prolonged monocular occlusion.

When binocular vision is prevented with monocular occlusion, the two eyes assume a position of rest related to the combination of underlying tonic innervation of the oculomotor system, cross-coupled accommodative-vergence input and vergence responses to perceptual cues for spatial location relative to the head. When the latter two are controlled, the covered eye has been shown in the majority of subjects to turn outward (exophoria) and upward (hyperphoria) after prolonged monocular occlusion. The present study investigates the change in torsional eye alignment and its relation to vertical eye alignment after eight hours of monocular occlusion. The results revealed an excyclophoria during occlusion in four out of five subjects. The patched eye also became elevated in two subjects and depressed in two others. Thus, during prolonged monocular occlusion, the relative directions of cyclophoria and vertical phoria appear to be independent. In addition, there were non-concomitant changes in vertical phoria with horizontal gaze, toward a state where the adducted eye was elevated relative to the abducted eye. Simulations with Orbit(TM) suggest that these non-concomitant changes in vertical phoria with a concomitant excyclophoria may be based upon orbital mechanics. Excyclophoria appears to be the baseline state of binocular alignment.

Humans↗

FPL and sweep VEP to tritan stimuli in young human infants.

Young infants can distinguish red from green without brightness cues which shows that neural pathways processing color information (the 'red-green' color-opponent pathway) are functional early in life. There is some doubt over whether the 'blue-yellow' pathway is functional in young infants. Here, we show that infants behave like tritanopic adults until 2-3 months post-term age. By 3-4 months, infants distinguish tritan stimuli, and therefore, the 'blue-yellow' pathway must be functional by that age. Our sweep visual evoked potentials to identical stimuli, however, are not significantly above noise levels, in disagreement with the behavioral responses. We discuss several possible explanations for the discrepancy.

Adult↗

Modulating motion-induced blindness with depth ordering and surface completion.

Motion-induced blindness is a striking phenomenon in which salient static visual stimuli "disappear" for seconds at a time in the presence of specific moving patterns. Here we investigate whether the phenomenon is due to surface completion of the moving patterns. Stereo-depth information was added to the motion stimulus to create depth ordering between the static and moving components of the display. Depth ordering consistent with the perceptual occlusion of the static elements increased motion-induced blindness whereas placing the moving components behind the static elements decreased the static dot disappearance. In a second experiment we used an induced surface stimulus configuration to drive the motion-induced blindness phenomenon as further evidence of the importance of surface completion and interactions during visual processing.

Analysis of Variance↗