Biomedical subjects

Haluk Ogmen

Publications and source records attributed to Haluk Ogmen.

5 recordsLinked to original sources

PubMed2004

Unconscious priming by color and form: different processes and levels.

Using a metacontrast masking paradigm, prior studies have shown (a) that a target's color information and form information, can be processed without awareness and (b) that unconscious color processing occurs at early, wavelength-dependent levels in the cortical information processing hierarchy. Here we used a combination of paracontrast and metacontrast masking techniques to explore unconscious color and form priming effects produced by blue, green, and neutral stimuli. We found that color priming in normal observers is significantly reduced when an additional paracontrast mask precedes the target at optimal masking SOAs. However, no reduction of form-priming effects was obtained at similar optimal paracontrast SOAs. We conclude that unconscious color priming depends on an early, wavelength- or stimulus-dependent response of color neurons located at early cortical levels whereas unconscious form priming occurs at later levels.

Adult↗

PubMed2004

A comparison of masking by visual and transcranial magnetic stimulation: implications for the study of conscious and unconscious visual processing.

Visual stimuli as well as transcranial magnetic stimulation (TMS) can be used: (1) to suppress the visibility of a target and (2) to recover the visibility of a target that has been suppressed by another mask. Both types of stimulation thus provide useful methods for studying the microgenesis of object perception. We first review evidence of similarities between the processes by which a TMS mask and a visual mask can either suppress the visibility of targets or recover such suppressed visibility. However, we then also point out a significant difference that has important implications for the study of the time course of unconscious and conscious visual information processing and for theoretical accounts of the processes involved. We present evidence and arguments showing: (a) that visual masking techniques, by revealing more detailed aspects of target masking and target recovery, support a theoretical approach to visual masking and visual perception that must take into account activities in two separate neural channels or processing streams and, as a corollary, (b) that at the current stage of methodological sophistication visual masks, by acting in more highly specifiable ways on these pathways, provide information about the microgenesis of form perception not available with TMS masks.

Consciousness↗

PubMed2003

The what and where in visual masking.

A metacontrast mask suppresses the visibility of, without influencing the reaction time (RT) to, the target. We investigated whether this dissociation results from a sensori-motor pathway immune to masking effects or from the characteristics of stimulus timing in mutually inhibitory sustained and transient channels. For target visibility, para- and metacontrast yielded the usual U-shaped functions. Peak paracontrast occurred at stimulus onset asynchronies (SOAs) of -150 to -100 ms. RTs were relatively low for metacontrast and did not show a systematic change as a function of SOA. The RT contribution from contour-masking was greatest at an SOA of -150 ms (paracontrast) and declined to near zero in the metacontrast regime. The dissociation between visibility and RT seen in metacontrast did not occur in paracontrast, rejecting the theory that RTs are elicited by a single sensori-motor pathway immune to masking. The dependence of the dissociation on stimulus timing can be explained by RECOD, a dual-pathway model wherein fast and slow activities interact.

Contrast Sensitivity↗

PubMed2003

Color and motion: which is the tortoise and which is the hare?

Recent psychophysical studies have been interpreted to indicate that the perception of motion temporally either lags or is synchronous with the perception of color. These results appear to be at odds with neurophysiological data, which show that the average response-onset latency is shorter in the cortical areas responsible for motion (e.g., MT and MST) than for color processing (e.g., V4). The purpose of this study was to compare the perceptual asynchrony between motion and color on two psychophysical tasks. In the color correspondence task, observers indicated the predominant color of an 18 degrees x 18 degrees field of colored dots when they moved in a specific direction. On each trial, the dots periodically changed color from red to green and moved cyclically at 15, 30 or 60 deg/s in two directions separated by 180 degrees, 135 degrees, 90 degrees or 45 degrees. In the temporal order judgment task, observers indicated whether a change in color occurred before or after a change in motion, within a single cycle of the moving-dot stimulus. In the color correspondence task, we found that the perceptual asynchrony between color and motion depends on the difference in directions within the motion cycle, but does not depend on the dot velocity. In the temporal order judgment task, the perceptual asynchrony is substantially shorter than for the color correspondence task, and does not depend on the change in motion direction or the dot velocity. These findings suggest that it is inappropriate to interpret previous psychophysical results as evidence that motion perception generally lags color perception. We discuss our data in the context of a "two-stage sustained-transient" functional model for the processing of various perceptual attributes.

Analysis of Variance↗

PubMed2003

Stereoscopic depth perception from oblique phase disparities.

In order to understand the role of oblique retinal image disparities in the perception of stereoscopic depth, we measured the depth perceived from random dot stereograms in which phase disparities were introduced in a selected band of stimulus orientations. A band of orientation was defined by a center orientation that ranged from 7.5 (near vertical) to 82.5 o[rientation]deg and by a bandwidth that was defined as the difference between the highest and the lowest orientation in the band. The bandwidths tested were 15, 30 and 45 odeg. A constant phase disparity of 90 p[hase]deg was introduced in all of the oriented spatial frequency components within the orientation band and the perceived depth of each stimulus was matched using a small square binocular probe. For each bandwidth, perceived depth increased with an increase in the center orientation up to approximately 60 odeg. This suggests that the human stereovision system derives a large proportion of information about perceived stereoscopic depth from oblique phase disparities. Simulations using an energy model of stereoscopic depth perception indicate that oblique phase disparities are unlikely to be processed by neural mechanisms tuned to near-vertical orientations within the stimulus. Our results therefore suggest that oblique retinal disparities are initially detected as oblique phase disparities by binocular mechanisms tuned to oblique orientations. Because the perceived depth from oblique phase disparities is consistent with the trigonometrically determined equivalent horizontal disparities, we presume that the information from oblique phase disparities is included in the visual system's computation of the horizontal retinal disparity.

Analysis of Variance↗