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Kevin R Brooks

Publications and source records attributed to Kevin R Brooks.

10 recordsLinked to original sources

Spatial scale of stereomotion speed processing.

To examine the spatial scale of the mechanisms supporting the perception of motion in depth defined by binocular cues, we measured stereomotion speed discrimination thresholds as a function of stimulus size using a two-interval speed comparison task. Stimuli were either random dot stereogram (RDS) bars featuring both the changing disparity (CD) and the interocular velocity difference (IOVD) cues to motion in depth or dynamic random dot stereogram (DRDS) bars featuring the CD cue alone. Monocular speed discrimination performance was also assessed, using half-images of the RDS stimulus. In addition, subjects' stereoacuity for stationary versions of the binocular stimuli was measured. Stimuli ranged in vertical extent from 1.25 to 40 min. Sensitivity to speed differences was strongly related to stimulus height for DRDS stimuli. Performance decreased rapidly as stimulus size was reduced, becoming nearly random for heights below 5 min. However, for RDS stimuli, speed discrimination performance declined with reductions in stimulus size at a far slower rate, providing superior performance at every stimulus size used. Monocular performance was superior still for the majority of subjects, yet showed a similar rate of decline to binocular RDS stimuli. We conclude that the spatial resolution of the CD mechanism and its static disparity inputs is, on average, nearly nine times more coarse than the IOVD system and its monocular motion inputs. Static stereoacuity controls show that this finding cannot be explained by differences in the disparity signals available in our RDS and DRDS stimuli.

Cues↗

Stereomotion suppression and the perception of speed: accuracy and precision as a function of 3D trajectory.

The precision and accuracy of speed discrimination performance for stereomotion stimuli were assessed for several receding 3D trajectories confined to the horizontal meridian. It has previously been demonstrated in a variety of tasks that detection thresholds are substantially higher when subjects observe a stereomotion stimulus than when simply viewing one of its component monocular half-images--a phenomenon known as stereomotion suppression (C. W. Tyler, 1971). Using monocularly visible motion in depth targets, we found mean speed discrimination thresholds to be higher for stereomotion, compared with monocular lateral speed discrimination thresholds for equivalent stimuli, demonstrating a disadvantage for binocular viewing in the case of speed discrimination as well. Furthermore, speed discrimination thresholds for motion in depth were not systematically affected by trajectory angle; hence, the disadvantage of binocular viewing persists even when there are concurrent changes in binocular visual direction. Lastly, there was a tendency for oblique trajectories of stereomotion to be perceived as faster than equally rapid motion receding directly away from the subject along the midline. Our data, in addition to earlier stereomotion suppression observations, are consistent with a stereomotion system that takes a noisy, weighted difference of the stimulus velocities in the two eyes to compute motion in depth.

Depth Perception↗

The swinging doors of perception: stereomotion without binocular matching.

Until recently, it was considered necessary for features in the two eyes to be matched before the evaluation of differences in their locations (binocular disparities) could reveal depth information. Motion in depth can also be perceived binocularly from related changes in the locations of matched binocular features. However, unmatched features can arise when a binocular object occludes more distant features in one eye but not the other. The presence and extent of such features can provide quantitative depth information, although perceived depth relative to geometrical predictions may vary from one such arrangement to another. The ability of humans to perceive motion in depth from unmatched stimuli has not previously been explored. Here, we use B. Gillam, S. Blackburn, and K. Nakayama's (1999) "monocular gap" stimuli to investigate perception of motion in depth simulated by a change in the extent of a monocularly occluded feature in a binocular display. Settings of a motion in depth probe revealed that the magnitude of perceived motion in depth is generally as large as that for a stimulus containing matchable binocular features. We show that our stimuli provide disambiguating information not present in similar static stimuli. We conclude that in the computation of motion in depth, a binocular match is not required. A new cue-dynamic half-occlusion-can be used to reach an accurate percept.

Depth Perception↗

Monocular transparency and unpaired stereopsis.

Howard and Duke [Howard, I. P. & Duke, P. A. (2003). Monocular transparency generates quantitative depth. Vision Research, 43, 2615-2621] recently proposed a new source of binocular information they claim is used to recover depth in stereoscopic displays. They argued that these displays lack conventional disparity and that the metrical depth experienced results from transparency rather than occlusion relations. Using a variety of modified versions of their stimuli, we show here that the conditions for transparency are not required to elicit the depth experienced in their stereograms. We demonstrate that quantitative and precise depth depended not on the presence of transparency but horizontal contours of the same contrast polarity. Depth was attenuated, particularly at larger target offsets, when horizontal contours had opposite contrast polarity for at least a portion of their length. We also show that a demonstration they used to control for the role of horizontal contours can be understood with previously identified mechanisms involved in the computations associated with stereoscopic occlusion. These results imply that the findings reported by Howard and Duke can be understood with mechanisms responsible for the computation of binocular disparity and stereoscopic occlusion.

Contrast Sensitivity↗

Monocular transparency and unpaired stereopsis.

Howard and Duke [Howard, I. P. & Duke, P. A. (2003). Monocular transparency generates quantitative depth. Vision Research, 43, 2615-2621] recently proposed a new source of binocular information they claim is used to recover depth in stereoscopic displays. They argued that these displays lack conventional disparity and that the metrical depth experienced results from transparency rather than occlusion relations. Using a variety of modified versions of their stimuli, we show here that the conditions for transparency are not required to elicit the depth experienced in their stereograms. We demonstrate that quantitative and precise depth depended not on the presence of transparency but horizontal contours of the same contrast polarity. Depth was attenuated, particularly at larger target offsets, when horizontal contours had opposite contrast polarity for at least a portion of their length. We also show that a demonstration they used to control for the role of horizontal contours can be understood with previously identified mechanisms involved in the computations associated with stereoscopic occlusion. These results imply that the findings reported by Howard and Duke can be understood with mechanisms responsible for the computation of binocular disparity and stereoscopic occlusion.

Contrast Sensitivity↗

Immune function biomarkers in children exposed to lead and organochlorine compounds: a cross-sectional study.

BACKGROUND: Different organochlorines and lead (Pb) have been shown to have immunomodulating properties. Children are at greater risk for exposure to these environmental toxicants, but very little data exist on simultaneous exposures to these substances. METHODS: We investigated whether the organochlorine compounds (OC) dichlorodiphenylethylene (DDE), hexachlorobenzene (HCB), hexachlorocyclohexane (gamma-HCH), the sum of polychlorinated biphenyls (SigmaPCBs) and Pb were associated with immune markers such as immunoglobulin (Ig) levels, white blood cell (WBC), counts of lymphocytes; eosinophils and their eosinophilic granula as well as IgE count on basophils. The investigation was part of a cross-sectional environmental study in Hesse, Germany. In 1995, exposure to OC and Pb were determined, questionnaire data collected and immune markers quantified in 331 children. For the analyses, exposure (OC and Pb) concentrations were grouped in quartiles (gamma-HCH into tertiles). Using linear regression, controlling for age, gender, passive smoking, serum lipids, and infections in the previous 12 months, we assessed the association between exposures and immune markers. Adjusted geometric means are provided for the different exposure levels. RESULTS: Geometric means were: DDE 0.32 microg/L, SigmaPCBs 0.50 microg/L, HCB 0.22 microg/L, gamma-HCH 0.02 microg/L and Pb 26.8 microg/L. The SigmaPCBs was significantly associated with increased IgM levels, whereas HCB was inversely related to IgM. There was a higher number of NK cells (CD56+) with increased gamma-HCH concentrations. At higher lead concentrations we saw increased IgE levels. DDE showed the most associations with significant increases in WBC count, in IgE count on basophils, IgE, IgG, and IgA levels. DDE was also found to significantly decrease eosinophilic granula content. CONCLUSION: Low-level exposures to OC and lead (Pb) in children may have immunomodulating effects. The increased IgE levels, IgE count on basophils, and the reduction of eosinophilic granula at higher DDE concentrations showed a most consistent pattern, which could be of clinical importance in the etiology of allergic diseases.

B-Lymphocytes↗

Stereomotion speed perception: contributions from both changing disparity and interocular velocity difference over a range of relative disparities.

The role of two binocular cues to motion in depth-changing disparity (CD) and interocular velocity difference (IOVD)- was investigated by measuring stereomotion speed discrimination and static disparity discrimination performance (stereoacuity). Speed discrimination thresholds were assessed both for random dot stereograms (RDS), and for their temporally uncorrelated equivalents, dynamic random dot stereograms (DRDS), at relative disparity pedestals of -19, 0, and +19 arcmin. While RDS stimuli contain both CD and IOVD cues, DRDS stimuli carry only CD information. On average, thresholds were a factor of 1.7 higher for DRDS than for RDS stimuli with no clear effect of relative disparity pedestal. Results were similar for approaching and receding targets. Variations in stimulus duration had no significant effect on thresholds, and there was no observed correlation between stimulus displacement and perceived speed, confirming that subjects responded to stimulus speed in each condition. Stereoacuity was equally good for our RDS and DRDS stimuli, showing that the difference in stereomotion speed discrimination performance for these stimuli was not due to any difference in the precision of the disparity cue. In addition, when we altered stereomotion stimulus trajectory by independently manipulating the speeds and directions of its monocular half-images, perceived stereomotion speed remained accurate. This finding is inconsistent with response strategies based on properties of either monocular half-image motion, or any ad hoc combination of the monocular speeds. We conclude that although subjects are able to discriminate stereomotion speed reliably on the basis of CD information alone, IOVD provides a precise additional cue to stereomotion speed perception.

Depth Perception↗

Human discrimination of visual direction of motion with and without smooth pursuit eye movements.

It has long been known that ocular pursuit of a moving target has a major influence on its perceived speed (Aubert, 1886; Fleischl, 1882). However, little is known about the effect of smooth pursuit on the perception of target direction. Here we compare the precision of human visual-direction judgments under two oculomotor conditions (pursuit vs. fixation). We also examine the impact of stimulus duration (200 ms vs. ~800 ms) and absolute direction (cardinal vs. oblique). Our main finding is that direction discrimination thresholds in the fixation and pursuit conditions are indistinguishable. Furthermore, the two oculomotor conditions showed oblique effects of similar magnitudes. These data suggest that the neural direction signals supporting perception are the same with or without pursuit, despite remarkably different retinal stimulation. During fixation, the stimulus information is restricted to large, purely peripheral retinal motion, while during steady-state pursuit, the stimulus information consists of small, unreliable foveal retinal motion and a large efference-copy signal. A parsimonious explanation of our findings is that the signal limiting the precision of direction judgments is a neural estimate of target motion in head-centered (or world-centered) coordinates (i.e., a combined retinal and eye motion signal) as found in the medial superior temporal area (MST), and not simply an estimate of retinal motion as found in the middle temporal area (MT).

Discriminant Analysis↗

Interocular velocity difference contributes to stereomotion speed perception.

Two experiments are presented assessing the contributions of the rate of change of disparity (CD) and interocular velocity difference (IOVD) cues to stereomotion speed perception. Using a two-interval forced-choice paradigm, the perceived speed of directly approaching and receding stereomotion and of monocular lateral motion in random dot stereogram (RDS) targets was measured. Prior adaptation using dysjunctively moving random dot stimuli induced a velocity aftereffect (VAE). The degree of interocular correlation in the adapting images was manipulated to assess the effectiveness of each cue. While correlated adaptation involved a conventional RDS stimulus, containing both IOVD and CD cues, uncorrelated adaptation featured an independent dot array in each monocular half-image, and hence lacked a coherent disparity signal. Adaptation produced a larger VAE for stereomotion than for monocular lateral motion, implying effects at neural sites beyond that of binocular combination. For motion passing through the horopter, correlated and uncorrelated adaptation stimuli produced equivalent stereomotion VAEs. The possibility that these results were due to the adaptation of a CD mechanism through random matches in the uncorrelated stimulus was discounted in a control experiment. Here both simultaneous and sequential adaptation of left and right eyes produced similar stereomotion VAEs. Motion at uncrossed disparities was also affected by both correlated and uncorrelated adaptation stimuli, but showed a significantly greater VAE in response to the former. These results show that (1) there are two separate, specialised mechanisms for encoding stereomotion: one through IOVD, the other through CD; (2) the IOVD cue dominates the perception of stereomotion speed for stimuli passing through the horopter; and (3) at a disparity pedestal both the IOVD and the CD cues have a significant influence.

Adaptation, Ocular↗

Monocular motion adaptation affects the perceived trajectory of stereomotion.

Perceived stereomotion trajectory was measured before and after adaptation to lateral motion in the dominant or nondominant eye to assess the relative contributions of 2 cues: changing disparity and interocular velocity difference. Perceived speed for monocular lateral motion and perceived binocular visual direction (BVD) was also assessed. Unlike stereomotion trajectory perception, the BVD of static targets showed an ocular dominance bias, even without adaptation. Adaptation caused equivalent biases in perceived trajectory and monocular motion speed, without significantly affecting perceived BVD. Predictions from monocular motion data closely match trajectory perception data, unlike those from BVD sources. The results suggest that the interocular velocity differences make a significant contribution to stereomotion trajectory perception.

Adaptation, Psychological↗