Search PubMed⌕ Search

Biomedical subjects

R Blake

Publications and source records attributed to R Blake.

At least 73 records · Page 4Linked to original sources

Spatial zones of binocular rivalry in central and peripheral vision.

This paper presents results from psychophysical experiments on human binocular rivalry in central and peripheral vision. Results show that the incidence of periods of exclusive visibility of a given eye's rival target increased with decreasing target size, and for a given sized target exclusive visibility increased with retinal eccentricity. Control measures confirmed that these results were not attributable solely to reduced peripheral acuity, to Troxler's effect, or to spatial frequency. We computed the minimum-sized stimulus that would lead to a criterion level of exclusive visibility of one or the other eye; this we term the spatial zone of binocular rivalry. The change in estimated size of spatial zones of rivalry with eccentricity compares favorably with estimates of human cortical magnification. We propose a model that assumes concentrically organized zones of rivalry. These zones do not function independently, but instead exhibit a high degree of mutual excitatory cooperativity. The model has multiple solutions for the foveal zone size, but the best fits predict a diameter of 5.3 or 7.3 min of visual angle; these values dovetail nicely with our empirical estimates of the foveal zone size.

Humans↗

Binocular rivalry suppression disrupts recovery from motion adaptation.

The motion aftereffect (MAE) lasts longer when the test period does not immediately follow adaptation, a phenomenon called storage. Does storage of the MAE occur if the test target is present but rendered phenomenally invisible owing to the presence of a rival target presented to the other eye during the storage period? Our experiment addressed this question. Following adaptation to a drifting grating, an intervening period preceded testing with a stationary grating. During this period, the adapted eye either viewed the test target immediately or was occluded, and the unadapted eye either viewed a high-contrast rival target or was occluded. Thus four conditions were employed. The duration of the residual MAE was found to be longer for the rivalry condition (grating and rival target viewed) than for the normal MAE condition (grating viewed), and comparable to that in the stored MAE condition (both eyes occluded). Thus, the MAE is stored when the test target is rendered invisible due to binocular rivalry, indicating that a suppressed target is ineffective at promoting decay of the MAE. So while suppression does not prevent information about the adapting grating from reaching the site of generation of the MAE (Lehmkuhle & Fox, 1975), it can prevent information about the test target from reaching the site of the stored MAE. Current models attribute the MAE to reduced responsiveness of direction-selective cortical neurons (Sutherland, 1961; Barlow & Hill, 1963). Thus, storage should reflect a differential return of these adapted cells to preadapted response levels, dependent on postadaptation stimulation.(ABSTRACT TRUNCATED AT 250 WORDS)

Adaptation, Ocular↗

Spatial interactions in binocular rivalry.

Observers tracked binocular rivalry between a pair of small, foveally viewed gratings whose orientation differed between the 2 eyes. In Experiment 1, a textured annulus surrounding 1 eye's grating increased the total duration of exclusive visibility of the grating only when the grating-annulus separation was less than 0.5 degree. In Experiment 2, observers tracked the visibility of a monocular annulus that surrounded a foveally viewed grating that was either engaged in rivalry or fused with a grating alone viewed by the other eye. The visibility of the annulus was greater when the grating it surrounded was not undergoing rivalry fluctuations. In Experiment 3, the predominance of a rival grating was greater when the contours in the surrounding annulus were orthogonal to those of the rival grating. In Experiment 4, total exclusive visibility of a given grating-annulus target was greater when the grating and the annulus contained the same orientation.

Adult↗

Do recognizable figures enjoy an advantage in binocular rivalry?

Five experiments examined whether recognizable stimuli predominate in binocular rivalry. It was found that a face predominated more than did a pattern equated for spatial frequency, luminance, and contrast; an objective reaction time procedure confirmed predominance of the face. The face was still liable to fragmentation as stimulus size increased. Observers tracked exclusive dominance of a picture of a camouflaged figure (a Dalmatian dog) prior to and then following discovery of the figure's presence; control observers received the same protocol with a scrambled version of the dog stimulus. Compared with control results, predominance of the dog picture was higher even before observers knew of the camouflaged figure. Inversion of the dog figure reduced its predominance. Binocular rivalry is sensitive to object-related, configural properties of a stimulus.

Attention↗

On the variety of percepts associated with dichoptic viewing of dissimilar monocular stimuli.

Upon dichoptic viewing of dissimilar patterns, several distinct perceptual states may be experienced over time. One state is exclusive monocular dominance, wherein the view of only one eye is seen in its entirety for some period of time. Another state is characterized by a mosaic-like college consisting of portions of the view of each eye. Two other states involve simultaneous perception of both monocular images in their entirety. In one of these states, the two monocular stimuli appear to be superimposed without depth (a phenomenon we shall term 'superimposition'). In the other state, the two monocular stimuli appear to be located at different depth planes (which we shall term 'transparency'). This paper documents the stimulus conditions favoring these various perceptual states. Exclusive monocular dominance occurs most often when the two eyes view dissimilar patterns with the same spatial-frequency content, particularly when both patterns consist of low spatial frequencies. Superimposition also occurs most often when the two eyes view the same spatial frequencies, but predominantly when those spatial frequencies are high. Transparency is favored when the spatial-frequency difference between the eyes is great, particularly when the view of one eye consists of high spatial-frequency information.

Depth Perception↗

A human visual disorder resembling area V4 dysfunction in the monkey.

We surveyed a broad range of visual functions in a man who complained of abnormal color experience and inability to recognize faces following bilateral damage in the visual cortex. A lesion in his right visual cortex caused complete left visual field loss. A lesion in his left visual cortex, located entirely below the calcarine fissure, affected the vision in his remaining hemifield, the right one. Psychophysical testing showed severely defective color vision and pattern processing, but relatively normal luminance contrast detection thresholds. The finding of normal spatial contrast sensitivity and static stereopsis did not resemble a parvocellular defect of the type described in the monkey. The abilities to detect global coherent motion among noise, structure from motion and dynamic stereopsis, and to pursue moving targets showed normal motion processing at several levels. Together with normal flicker perception, these results excluded magnocellular or MT-like defects. Altogether, the findings mimic area V4 dysfunction.

Adult↗

Urea kinetics has limited relevance in assessing adequacy of dialysis in CAPD.

The application of urea kinetics to CAPD is controversial. Additional data is presented from our recent study on this topic. Different methods of calculating KT/V and normalized protein catabolic rate (PCRN) are compared and KT/V is shown to be on average 6.5% higher when V is calculated by Watson's formulae instead of by body weight alone. This discrepancy increases with time. It is also shown that standard methods may overestimate KT and underestimate PCRN. KT/V and PCRN by these different methods do not correlate with clinical outcomes. However, if V is calculated by Watson's formulae, there is a significant excess of deaths when KT/V is under 0.5 (weekly KT/V under 1.5). Survival curves show that neither initial KT/V nor PCRN predict failure on CAPD.

Female↗

Chloroquine therapy in psoriatic arthritis.

Our aim was to examine the efficacy of chloroquine in psoriatic arthritis (PsA) and to assess whether chloroquine therapy exacerbated psoriasis. Thirty-two patients had been given chloroquine therapy while attending the University of Toronto Psoriatic Arthritis Clinic. Twenty-four patients continued therapy for at least 6 months, and 18, or 75%, demonstrated > 30% reduction in the actively inflamed joint count. Moreover, there was a significant decrease in the number of actively inflamed joints. A control group, consisting of 24 patients taking no remittive agents, seen during the same period of time, was identified. Only 14, or 58%, of these patients had a > 30% reduction in inflamed joint count over a 6-month period. This pattern was not significantly different (p = 0.19) from the chloroquine treated group. Of the 32 patients who had been given chloroquine, a total of 6 had an exacerbation of psoriasis, only 1 discontinued therapy. There was no case of exfoliative dermatitis. Six of the 24 control patients had an exacerbation of psoriasis. Our experience suggests that chloroquine may be an effective treatment in PsA, and that it does not exacerbate psoriasis. A prospective, randomized, double blind, controlled trial of antimalarial therapy in PsA is warranted.

Administration, Oral↗

Relation between fibrositic and control site tenderness; effects of dolorimeter scale length and footplate size.

Recent data have suggested a correlation between the tenderness measured at tender and control sites, differing from earlier studies indicating site specific tenderness. In our study, the "constant control" model is tested against the "correlated control" model, in which control site tenderness varies with fibrositic site tenderness. Our study also addresses relevant technical issues in dolorimetry. We measured threshold of tenderness at 4 sites (2 fibrositic and 2 control) on 21 subjects, using dolorimeters with a 17 kg scale limit, and 3 different footplates, 0.7, 1.4 and 2.0 cm in diameter. To measure observer variation, we used multiple replications by multiple observers, obtaining in all 1,416 observations. There was a strong relationship between control and fibrositic site tenderness with control thresholds twice as high (half as tender). Scale length and dolorimeter footplate size each had important effects. The site specific approach is valuable diagnostically, but more broadly operative mechanisms should be the focus of research and therapy.

Adult↗

Mixed ligand complexes of iron with cyanide and phenanthroline as new probes of metalloprotein electron transfer reactivity. Analysis of reactions involving rusticyanin from Thiobacillus ferrooxidans.

A family of 12 different mixed ligand complexes of iron with cyanide and substituted 1,10-phenanthroline was prepared. The electron transfer properties of each reagent were systematically manipulated by varying the substituent(s) on the aromatic ring system and the stoichiometry of the two types of ligands in the complex. Values for the standard reduction potentials of each member of this family of electron transfer reagents were determined and spanned from 500 to 900 mV. The one-electron transfer reactions between each of these substitution-inert reagents and the high potential blue copper protein, rusticyanin, from Thiobacillus ferrooxidans were studied by stopped flow spectrophotometry under acidic conditions. For comparison with the protein results, the kinetics of electron transfer between each of these reagents and sulfatoiron were also investigated. The Marcus theory of electron transfer was successfully applied to this set of kinetic data to demonstrate that 10 of the 12 reagents had equal kinetic access to the redox center of the rusticyanin and utilized the same reaction pathway for electron transfer. The utility of these synthetic electron transfer reagents in characterizing the electron transfer properties of very high potential, redox-active metalloproteins is illustrated.

Azurin↗

Spatial frequency tuning of human stereopsis.

A masking paradigm was employed to measure the spatial frequency selectivity of channels underlying human stereopsis. Observers viewed spatially filtered (0.4 octave bandwidth) random-dot stereograms in which a disparate bar appeared in either the top or bottom half of the display; superimposed on one RDS half-image was a noise target whose spatial frequency content was varied relative to that of the RDS. A staircase procedure was used to measure the monocular noise energy (and hence the signal-to-noise ratio) at which observers could judge the location of the disparate bar on 71% of trials. Statistical analyses showed that the resulting stereoscopic masking functions could be grouped into two sets, one with peak sensitivity at 3 c/deg and the other with peak sensitivity at 5 c/deg. These two channels were observed for both crossed and uncrossed disparities ranging from coarse to fine. Essentially the same results were obtained with binocular noise and with stereo displays flashed too briefly to be affected by eye movements. Our results are inconsistent with models of stereopsis in which the disparity range to which a channel is sensitive varies with that channel's peak spatial frequency. These data imply that the spatial frequency selectivity of stereopsis differs from the tuning of spatial channels underlying the detection and discrimination of form.

Depth Perception↗

On the coexistence of stereopsis and binocular rivalry.

Dichoptically viewed complex texture stereograms with correlated spatial frequency information can yield stable depth perception, implying cooperative interaction between the two eyes. Dichoptically viewed dissimilar texture pairs may yield competition in the form of binocular rivalry. To study whether stereopsis and rivalry can spatially coexist when stimulus conditions for both are present, we had observers dichoptically view spatial frequency filtered random-dot patterns. The left eye viewed one half-image of an RDS; the right eye viewed the superimposition of the other RDS half-image (which when paired alone with the left-eye RDS yielded stereoscopic depth) and a noise target (which on its own engaged in rivalry with the right eye target). Observers judged the quality of depth and the rate of rivalry for these stereo-pairs. When the contrast of the noise component was low, observers experienced stereopsis and stable single vision that included the noise. At intermediate noise contrasts, local regions were seen either in rivalry or in stereoscopic depth, but rivalry and depth were not experienced at the same spatial location simultaneously. At high noise contrasts, the right eye target dominated almost exclusively, with little hint of stereopsis. Essentially the same pattern of results was obtained in forced-choice experiments in which observers judged the direction of stereoscopic tilt from vertical cosine gratings differing slightly in spatial frequency. Considered together, these results are inconsistent with theories positing that rivalry and stereopsis coexist at the same spatial location because they occur within independent, parallel pathways.

Depth Perception↗

Apparent motion can survive binocular rivalry suppression.

For short-range motion, observers dichoptically viewed a random-dot cinematogram and a rival target. Upon keypress, the first frame of the cinematogram was replaced by the second frame. Observers judged the direction of motion, which was governed by the initial position of the central region. Performance was well above chance during both dominance and suppression. For long-range motion, observers rated the motion produced by sequentially flashing two small spots, with the first spot contained within a rivalrous region. Suppression reduced but did not prevent perception of this motion. Presenting the second motion frame to both eyes weakened both forms of motion.

Female↗

Neural models of stereoscopic vision.

Human stereopsis remains an enigma: how does the brain match features between the left and right eye images and compute disparity between these matched features? Developments in computational neuroscience and machine vision have led to several models of human stereopsis that provide insight into possible mechanisms underlying this phenomenon. These models, reviewed in this paper, adopt one of three general strategies. One class of models employs cooperative interactions, whereby a unique solution to the matching problem emerges from excitatory and inhibitory interactions among binocular neural elements. A second class of models implements matching and disparity computation serially over multiple spatial scales. A third class relies on local, non-interacting computations performed in parallel to overcome speed limitations inherent in the other models. Considered together, these theoretical developments offer fresh insights concerning the actual neural concomitants of binocular stereopsis.

Animals↗

A neural network model of kinetic depth.

We propose a network model that accounts for the kinetic depth in structure from motion phenomena. Using plausible neural mechanisms, the model accounts for (1) fluctuations in perception when viewing a simple kinetic depth stimulus, (2) disambiguation of this stimulus with stereoscopic information, and (3) subsequent bias of the percept of this stimulus following stereoscopic adaptation. The model comprises two levels: a layer of monocular directionally selective motion detectors that provide input to a second layer of disparity-selective and direction-selective binocular mechanisms. The network of facilitatory and inhibitory connections between binocular mechanisms gives rise to fluctuations in network activity that mimic the fluctuations in perception of kinetic depth in the absence of disparity information. The results of a psychophysical experiment are consistent with the nature of the proposed interactions.

Adaptation, Ocular↗

Coarse spatial scales constrain the range of binocular fusion on fine scales.

To examine interactions among spatial scales in disparity processing, we have measured the upper disparity limit for binocular single vision (the diplopia threshold) for high-spatial-frequency test stimuli in the presence of cosine gratings of lower spatial frequency that defined a surface in depth. When the frequency of this grating surface was 2.0 octaves below that of the test, the test fusion range was reduced by a factor of 3-4 relative to the condition in which no grating surface was present. However, gratings 4.0 octaves below the test frequency had no effect, and the test and grating were seen transparently at different depths. Further experiments indicate that the effect is orientation specific and that high-frequency gratings do not affect low-frequency tests. Finally, experiments using grating surfaces tilted in depth indicate that fusion at high spatial frequencies is constrained to a range centered on the local disparity of the surface defined by the lower frequency. These results are important for computational models for stereopsis that are based on coarse-to-fine matching strategies.

Depth Perception↗

The interplay between stereopsis and structure from motion.

In a series of psychophysical experiments, an adaptation paradigm was employed to study the influence of stereopsis on perception of rotation in an ambiguous kinetic depth (KD) display. Without prior adaptation or stereopsis, a rotating globe undergoes spontaneous reversals in perceived direction of rotation, with successive durations of perceived rotation being random variables. Following 90 sec of viewing a stereoscopic globe undergoing unambiguous rotation, the KD globe appeared to rotate in a direction opposite that experienced during the stereoscopic adaptation period. This adaptation aftereffect was short-lived, and it occurred only when the adaptation and test figures stimulated the same retinal areas, and only when the adaptation and test figures rotated about the same axis. The aftereffect was just as strong when the test and adaptation figures had different shapes, as long as the adaptation figure contained multiple directions of motion imaged at different retinal disparities. Nonstereoscopic adaptation figures had no effect on the perceived direction of rotation of the ambiguous KD figure. These results imply that stereopsis and motion strongly interact in the specification of structure from motion, a result that complements earlier work on this problem.

Adaptation, Ocular↗