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Biomedical subjects

Anna Ma-Wyatt

Publications and source records attributed to Anna Ma-Wyatt.

7 recordsLinked to original sources

Visual information throughout a reach determines endpoint precision.

People make rapid, goal-directed movements to interact with their environment. Because these movements have consequences, it is important to be able to control them with a high level of precision and accuracy. Our hypothesis is that vision guides rapid hand movements, thereby enhancing their accuracy and precision. To test this idea, we asked observers to point to a briefly presented target (110 ms). We measured the impact of visual information on endpoint precision by using a shutter to close off view of the hand 50, 110 and 250 ms into the reach. We found that precision was degraded if the view of the hand was restricted at any time during the reach, despite the fact that the target disappeared long before the reach was completed. We therefore conclude that vision keeps the hand on the planned trajectory. We then investigated the effects of a perturbation of target position during the reach. For these experiments, the target remained visible until the reach was completed. The target position was shifted at 110, 180 or 250 ms into the reach. Early shifts in target position were easily compensated for, but late shifts led to a shift in the mean position of the endpoints; observers pointed to the center of the two locations, as a kind of best bet on the position of the target. Visual information is used to guide the hand throughout a reach and has a significant impact on endpoint precision.

Arm↗

Initial visual information determines endpoint precision for rapid pointing.

We investigated how visual noise in the initial estimate of target location affects precision for rapid pointing. Visual localization thresholds (an error measure) rise systematically with eccentricity, doubling at eccentricities of a degree or less. Previous work, which we confirmed, has shown that the precision of pointing, measured by the standard deviation, to a single isolated target is relatively constant over small lateral extents near the midline, and that pointing error is substantially larger than visual error. We used target uncertainty (randomly chosen locations) to greatly increase visual noise so that we could explore the influence of visual noise on pointing error. We compared precision for comparable visual and pointing tasks as a function of target eccentricity. The target was presented for 110 ms at one of eight isoeccentric locations, chosen at random. Under these conditions, pointing error increased significantly with increasing target eccentricity. Beyond 4 degrees eccentricity, visual thresholds and pointing error were identical. Even when the target remained visible until the movement was completed, initial target eccentricity affected pointing error. The quality of visual information varies with task demands, and therefore so does its influence on endpoint precision. Our results demonstrate that the initial visual information about target location can limit endpoint precision, even over as small a range as 12 degrees in the central visual field (a lateral extent of +/-8.5 cm at the midline).

Fingers↗

Seeing and ballistic pointing at perisaccadic targets.

We studied the effects of visual references and the level of illumination on the localization of stimuli flashed briefly near the start of saccades. A translucent shutter made it possible to remove visual references, but admit light, at different times after saccadic onset. The results show that post-saccadic visual references are not necessary for compression: a consistent compression of verbally reported relative stimulus distances is found at all shutter latencies and at all post-shutter levels of illumination. They also show that positions indicated by blind pointing show no compression except when visual references remain in view for a substantial time after saccades. These results confirm that the visual system uses multiple representations of space and suggest that it weights them differently for different tasks and different viewing conditions. No single map is used exclusively for conscious perception or for motor action, and conscious perception is always subject to compression at the time of saccades.

Darkness↗

Contrast configuration influences grouping in apparent motion.

We investigated whether the same principles that influence grouping in static displays also influence grouping in apparent motion. Using the Ternus display, we found that the proportion of group motion reports was influenced by changes in contrast configuration. Subjects made judgments of completion of these same configurations in a static display. Generally, contrast configurations that induced a high proportion of group motion responses were judged as more 'complete' in static displays. Using a stereo display, we then tested whether stereo information and T-junction information were critical for this increase in group motion. Perceived grouping was consistently higher for same contrast polarity configurations than for opposite contrast polarity configurations, regardless of the presence of stereo information or explicit T-junctions. Thus, while grouping in static and moving displays showed a similar dependence on contrast configuration, motion grouping showed little dependence on stereo or T-junction information.

Contrast Sensitivity↗

Saccades actively maintain perceptual continuity.

People make saccades--rapid eye movements to a new fixation--approximately three times per second. This would seemingly disrupt perceptual continuity, yet our brains construct a coherent, stable view of the world from these successive fixations. There is conflicting evidence regarding the effects of saccades on perceptual continuity: some studies report that they are disruptive, with little information carryover between saccades; others report that carryover is substantial. Here we show that saccades actively contribute to perceptual continuity in humans in two different ways. When bistable stimuli are presented intermittently, saccades executed during the blank interval shorten the duration of states of ambiguous figures, indicating that saccades can erase immediately past perceptual states. On the other hand, they prolong the McCollough effect, indicating that saccades strengthen learned contingencies. Our results indicate that saccades help, rather than hinder, perceptual continuity.

Adult↗

Developmental dyslexia in different languages: language-specific or universal?

Most of the research on developmental dyslexia comes from English-speaking countries. However, there is accumulating evidence that learning to read English is harder than learning to read other European orthographies (Seymour, Aro, & Erskine, 2003). These findings therefore suggest the need to determine whether the main English findings concerning dyslexia can be generalized to other European orthographies, all of which have less irregular spelling-to-sound correspondences than English. To do this, we conducted a study with German- and English-speaking children (n=149) in which we investigated a number of theoretically important marker effects of the reading process. The results clearly show that the similarities between dyslexic readers using different orthographies are far bigger than their differences. That is, dyslexics in both countries exhibit a reading speed deficit, a nonword reading deficit that is greater than their word reading deficit, and an extremely slow and serial phonological decoding mechanism. These problems were of similar size across orthographies and persisted even with respect to younger readers that were at the same reading level. Both groups showed that they could process larger orthographic units. However, the use of this information to supplement grapheme-phoneme decoding was not fully efficient for the English dyslexics.

Adolescent↗

Pattern cues disambiguate perceived direction in simple moving stimuli.

Much of our knowledge about motion perception has been obtained by studying bars moving within apertures. When viewed within an ambiguously oriented aperture such as a circle, bars appear to move orthogonal to their orientation. We demonstrate that if the local orientation of the aperture edges is altered, a direction consistent with the edge orientation is seen. Indeed, the perceived direction can be strongly influenced by static lines separated from the edge of the moving stimulus. These results support recent suggestions that precise motion direction is likely to be determined by static orientation cues.

Adult↗