Biomedical subjects

Sieu K Khuu

Publications and source records attributed to Sieu K Khuu.

7 recordsLinked to original sources

PubMed2006

The perceived position shift of a pattern that contains internal motion is accompanied by a change in the pattern's apparent size and shape.

When the sinusoidal grating of a "Gabor pattern" is drifted, the apparent position of the pattern shifts in the direction of motion [De Valois, R. L., & De Valois, K. K. (1991). Vernier acuity with stationary moving Gabors. Vision Research, 31, 1619-1626]. We investigated the underlying cause of this illusion by determining whether the effect is a consequence of the internal motion shifting the perceived position of the whole pattern, or a consequence of a shift in the perceived location of the centroid (centre of mass) of the Gabor envelope. While each of these two possible distortions can account for a perceived positional offset, they give different predictions for the apparent size of the stimulus. A simple shift in perceived position results in no change in apparent size, while a centroid shift will likely result in either a decrease or an increase in the pattern's apparent size, depending on whether the trailing or leading edge of the Gabor stimulus is most affected by motion. We examined whether there is a change in the apparent size of Gabor patterns containing a range of grating motion speeds. We found that the perceived size of the pattern increased in the presence of motion as a function of speed, and is thus consistent with a centroid-shift explanation. We verified that this size change is a consequence of an increase in contrast at the leading edge, since the leading edge appears elongated relative to the trailing edge. We furthermore showed that the apparent-position shifts due to motion can be negated by displacing the centroid in the opposite direction to the motion.

Contrast Sensitivity↗

PubMed2006

The role of luminance contrast in the detection of global structure in static and dynamic, same- and opposite-polarity, Glass patterns.

Perception of global structure conveyed in static Glass patterns is difficult, though not impossible, when the constituent dipoles are formed by partnering opposite polarity dots. We investigate whether the addition of motion signals to opposite-polarity Glass patterns can act to restore the perception of global structure. The stimuli were concentric Glass patterns consisting of 200 dipoles concentrically orientated, or oriented at random orientations, placed on a grey background. For each dipole, one luminance-increment dot (Weber contrast of 1) was paired with another dot set to a contrast ranging between luminance increment and luminance decrement (i.e., a Weber contrast range of approximately -1 to 1). Dipoles were either stationary (Experiment 1), or randomly re-positioned at 17Hz (Experiment 2), on each frame transition. A two-interval forced-choice paradigm, in conjunction with an adaptive staircase, was used to obtain Glass-pattern detection thresholds. The task required observers to identify the interval that contained concentric Glass structure; the other interval contained randomly orientated dipoles. Generally, lower global form thresholds were observed for dynamic and same-polarity Glass patterns than for static and opposite-polarity Glass patterns. In particular, for dynamic presentations improvement in sensitivity was more evident for opposite-polarity than for same-polarity Glass patterns. These findings suggest that motion plays an important role in the detection of global structure in dynamic Glass patterns.

Contrast Sensitivity↗

PubMed2006

Apparent position in depth of stationary moving three-dimensional objects.

Motion signals contained within a stationary object projected on the fronto-parallel plane shift the object's apparent spatial position in the direction of the motion [see De Valois, R. L., & De Valois, K. K. (1991). Vernier acuity with stationary moving Gabors. Vision Research, 31(9), 1619-1626]. We report an analogous apparent position shift of three-dimensional objects that contain local elements that move in depth. Our stimulus was a transparent three-dimensional cylinder defined by 150 limited-lifetime dots, oriented such that it was end on and its tangent plane was circular. Dots moved in depth by changes in their binocular disparities. In the first experiment, observers judged the positions of the near and far ends of the cylinder, by moving marker lines in depth, for different dot speeds. The results showed that when dots moved towards the observer, the perceived location of the two ends of the cylinder appeared closer in depth. When dots moved away from the observer, the opposite effect was produced. Additionally, the amount of apparent position shift produced was dependent on dot speed, with faster speeds producing larger positional offsets. However, we found in the second experiment that when the cylinder contained randomly moving dots, or when the cylinder contained equal amounts of dots moving towards and away from the observer, positional shifts were very much reduced, or abolished. Our findings suggest that motion signals can induce a misperception of position in depth that is similar manner to that produced by motion within an object in the two-dimensional image plane.

Cues↗

PubMed2005

Global speed averaging is tuned for binocular disparity.

The extent to which local speeds at different depths are averaged to determine global speed was determined using a version of the Global Dot Motion (GDM) stimulus. Judgments of the apparent speed of fast moving dots (4.05-10.53 deg/s) in the presence of slow moving dots (4.05 deg/s) were measured using GDM stimuli which simulated radially expanding motion, and which confined slow and fast speed dots exclusively to alternating wedge shaped sectors. The presence of slow moving dots in the stimulus reduced the apparent speed of high-speed dots in a manner consistent with speed averaging. However with increases in depth, produced by a difference in binocular disparity between dots in alternating sectors, speed averaging became less effective, and the relationship between speed and disparity resembled a tuning function. We discuss our results in light of research that clarifies the functional properties of global motion mechanisms in the primate cortex.

Animals↗

PubMed2005

Glass-pattern detection is tuned for stereo-depth.

We investigated the role of disparity information in the detection of global form. Glass patterns, which allow insight into processing at both local and global stages of form analysis, were used as stimuli. We determined how detection of concentric Glass patterns is affected by a disparity difference introduced between partner dots forming local dipoles (Experiment 1), and how detection is affected by the addition of randomly oriented dot-pairs (noise dots) at crossed and uncrossed disparities (Experiment 2). The first experiment showed that detection thresholds increased when partner dots were separated in depth at disparities greater than approximately 17 min arc; the second experiment showed that noise dots disrupted the detection of form if they were presented at disparities of between approximately +/-20 min arc from the Glass pattern's presentation depth plane. Our findings suggest that disparity information plays a role in the recovery of the image structure and, importantly, local and global form mechanisms were found to be selective for a small range of stereo-depths. We discuss the findings of our study in the light of current evidence indicating that a common neural substrate is responsible for the analysis of form and binocular disparity.

Attention↗

PubMed2005

Interactions between luminance and contrast signals in global form detection.

The human visual system is adept at detecting global structure, or form, within a scene. The initial stage of post-retinal processing for all aspects of vision is fed by On- and Off-centre cells sensitive to centred luminance increments and decrements respectively. These cells provide input to two parallel pathways that process variations in local luminance (first-order pathway) and local contrast (second-order pathway). Here, we investigate the contribution of luminance and contrast information to global form detection, a stage between the extraction of local orientation and the recognition of objects. The underlying processes involve two stages. We find that signals in the On-, Off- and second-order pathways are segregated at both stages of processing. Surprisingly, the non-linear stage in the second-order form pathway is different from that in motion processing: the second-order form detectors show an asymmetry in sensitivity to increments and decrements that is not apparent in motion. A functional architecture for global form detection is proposed along with its possible neural substrates.

Contrast Sensitivity↗

PubMed2002

Global speed processing: evidence for local averaging within, but not across two speed ranges.

A primary task of the visual system is to extract the direction and speed of animate objects from the retinal image. We examined global speed processing by determining how local speeds are integrated and whether integration occurs across all speeds or within fixed speed ranges. The first experiment addressed how local motion signals are combined to determine the speed of an object in motion. Observers judged the speed of a moving cloud of dots that took a random walk in direction while the dots inside the cloud moved somewhat independently of the cloud itself. The apparent speed of the cloud of dots is found to change in proportion with the dot speed and is well predicted by calculating the average speed resulting from nearest neighbour matches across stimulus frames. The second experiment addressed whether local speeds are combined across all speeds or within fixed speed ranges for the detection of global motion. Global dot motion (GDM) stimuli that moved in a radial or rotational directions moving at a low speed of 1.2 degrees /s or a high speed of 9.6 degrees /s were used to measure the thresholds for detecting structured motion as a function of the speed of noise dots (0 degrees /s-10.8 degrees /s) added to the stimulus. With low-speed targets, only additional noise dots moving at low speeds interfered with signal detection. High-speed targets were only interfered with by dots moving at high speeds. This finding established the existence of at least two independent speed tuned systems in the range of speeds tested. Experiment 3 investigated how speed signals are combined within a system to determine the global speed. Using sectored radial GDM stimuli the perceived speed of the fastest dots was measured as a function of whether the speed of the dots in alternate sectors either activated the high or low-speed systems. Averaging only occurred when dots were all within the sensitivity range of the high-speed system, however, if alternate sectors activated separate speed systems, averaging did not occur. Thus local speeds are averaged, independent of direction, to derive a global speed estimate, but averaging only occurs within, and not across, speed tuned mechanisms.

Adult↗