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Biomedical subjects

Jocelyn Faubert

Publications and source records attributed to Jocelyn Faubert.

At least 19 recordsLinked to original sources

Macular hole: perceptual filling-in across central scotomas.

The present study examined perceptual distortions of a vertical line before and after macular hole (MH) surgery in 25 eyes of 24 patients. Participants' perceptual reports of distortions were classified as solid, bent right/left, thinned at the center, or broken. The majority of patients (72%) reported symmetrical distortions of the line pre-operatively. After surgery, participants with larger MHs were more likely to retain residual distortions. Of particular interest is the group reporting thinning of the line preoperatively, as the center should be perceptually missing. Examination of MH diameters in relation to the line perceptions indicated that the shape of the perceived line can be explained at the retinal level, while its continuity must be perceptually created at the cortical level.

Adult↗

Same calculation efficiency but different internal noise for luminance- and contrast-modulated stimuli detection.

There is no consensus on whether luminance-modulated (LM) and contrast-modulated (CM) stimuli are processed by common or separate mechanisms. To investigate this, the sensitivity variations to these stimuli are generally compared as a function of different parameters (e.g., sensitivity as a function of the spatial or temporal window sizes) and similar properties have been observed. The present study targets the sensitivity difference between LM and CM stimuli processing. Therefore, instead of studying the variation of sensitivity in different conditions, we propose to decompose the sensitivities in internal equivalent noise (IEN) and calculation efficiency (CE) to evaluate at which processing level the two mechanisms differ. For each stimulus type, the IEN and CE of four observers were evaluated using three different carriers (plaid, checkerboard, and binary noise). No significant CE differences were noted in all six conditions (3 carriers x 2 modulation types), but important differences were found between the IEN of the two stimulus types. These data support the hypothesis that the two pathways are initially separate and that the two stimuli may be treated by common mechanisms at a later processing stage. Based on ideal observer analysis, pre-rectification internal noise could explain the difference of IEN between LM and CM stimuli detection when using binary noise as a carrier but not when using a plaid or a checkerboard. We conclude that a suboptimal rectification process causes higher IEN for CM stimuli detection compared with LM stimuli detection and that the intrinsic noise of the binary carrier had a greater impact on the IEN than the suboptimal rectification.

Adult↗

Demonstrations of decreased sensitivity to complex motion information not enough to propose an autism-specific neural etiology.

Interest regarding neural information processing in autism is growing because atypical perceptual abilities are a characteristic feature of persons with autism. Central to our review is how characteristic perceptual abilities, referred to as perceptual signatures, can be used to suggest a neural etiology that is specific to autism. We review evidence from studies assessing both motion and form perception and how the resulting perceptual signatures are interpreted within the context of two main hypotheses regarding information processing in autism: the pathway- and complexity-specific hypotheses. We present evidence suggesting that an autism-specific neural etiology based on perceptual abilities can only be made when particular experimental paradigms are used, and that such an etiology is most congruent with the complexity-specific hypothesis.

Autistic Disorder↗

Defining the nature of motion perception deficits in glaucoma using simple and complex motion stimuli.

PURPOSE: The purpose of this study is to determine the nature of motion perception deficits in primary open-angle glaucoma by measuring the sensitivity of simple (luminance-defined) and complex (texture-defined) motion, the latter requiring supplementary neural processing to be resolved. These findings will help address the possible extent of the cortical damage in glaucoma that has been recently demonstrated by anatomic and physiological studies. They also serve the purpose of establishing which motion paradigms would be most appropriate for assessing glaucoma-related functional loss. METHODS: Direction-identification thresholds for first-order and second-order motion were measured for 26 patients with primary open-angle glaucoma (for both phakic and pseudophakic) and 18 nonglaucomatous observers. RESULTS: The glaucomatous observers showed significantly increased motion thresholds for both first- and second-order motion conditions when compared with nonglaucomatous observers. However, the relative increase in threshold for first-order motion did not differ significantly from that of second-order motion. CONCLUSIONS: These findings imply that there is no measurable higher-level cortical function damage caused by the glaucomatous process because no greater loss in second-order motion was observed. Based on the results, we suggest that motion paradigms used to assess functional loss in primary open-angle glaucoma should consist of simple, first-order type stimuli to minimize potential confounds such as those introduced by both the normal and pathologic aging process on complex motion processing (i.e., perimetry using complex motion stimuli).

Aged↗

Effect of aging on stereoscopic interocular correlation.

PURPOSE: This study was designed to evaluate the minimum interocular correlation (IOC) needed by the visual system to correctly perceive a static stereoscopic stimulus as a function of normal aging. It was also our goal to evaluate the feasibility of clinical charts testing this aspect of visual perception. METHODS: Stereoscopic IOC threshold was determined in 100 normal observers (average age +/- standard deviation, 45.7 +/- 20.4 years) drawn from a clinical population between the ages of 10 and 85. We used partially correlated red-green random dot stereograms (RDS) displaying flat, square surfaces at 360 arcsec of either crossed or uncrossed disparity. RESULTS: Older observers needed a higher binocular correlation to perceive the stereoscopic stimuli when compared with the younger groups. There is a slight increase in the threshold value of the individuals in the 45- to 64-year-old group and a further effect on the observers over 65 years of age. Data did not reveal any effects of gender, near point phoria, or fixation disparity on IOC thresholds. CONCLUSIONS: Normal aging produces a statistically significant deficit in binocular correlation processing. This process is marginally correlated with stereo acuity measures even when stereoacuity floor effects are factored out. Although further experiments directly comparing stereoacuity and IOC are necessary and more refining is required to obtain optimum parameters, clinical stereoscopic IOC test charts appear feasible and may not assess the same processes as stereoacuity charts.

Adolescent↗

Chromatic parameters derived from increment spectral sensitivity functions.

We propose a mathematical model to derive the chromatic parameters from increment spectral sensitivity functions. This model was applied to determine the effective red, green, blue, and yellow mechanism contribution to the detection of the spectral stimuli of five normal trichromatic subjects. Detection thresholds were measured for a 300 ms, 1.2 degrees circular test flash presented on a 100 cd/m2 white background for spectral wavelengths between 410 and 660 nm. The model analysis confirmed that in the red-green wavelength area, the detection of our chosen stimuli was mediated by two distinct (L-M) antagonistic mechanisms: a red-green and a yellow, from the blue-yellow system. We inferred that the red-green mechanism receptive fields consisted of a single L- or M-cone center with a homogeneous or heterogeneous surround devoid of S-cone projections. For the receptive fields of the yellow half of the blue-yellow mechanism, we propose a similar configuration but with S-cone projections present in the surround. This proposal is not concordant with what is currently understood regarding retinal physiology. However, two L-M antagonistic mechanisms in the red-green wavelengths as proposed by our results predict what would appear as an intuitive yellow mechanism with a maximal sensitivity at the 578 nm wavelength, where the red-green mechanism sensitivity is null.

Journal Article↗

Recognition of faces and complex objects in younger and older adults.

We examined whether (1) age-associated impairments in face recognition are specific to faces or also apply to within-category recognition of other objects and (2) age-related face recognition deficits are related to impairments in encoding second-order relations and holistic information. In Experiments 1 and 2, we found reliable age differences for recognition of faces, but not of objects. Moreover, older adults (OAs) and younger adults (YAs) displayed similar face inversion effects. In Experiment 3, unlike YAs, OAs did not show the expected decline in performance for recognition of composites (Young, Hellawell, and Hay, 1987). In Experiment 4, both OAs and YAs showed a whole/part advantage (Tanaka and Farah, 1993). Our results suggest that OAs have spared function for processing of second-order relations and holistic information. Possible explanations for the finding that OAs have greater difficulty recognizing faces than recognizing other objects are proposed.

Adolescent↗

Enhanced and diminished visuo-spatial information processing in autism depends on stimulus complexity.

Visuo-perceptual processing in autism is characterized by intact or enhanced performance on static spatial tasks and inferior performance on dynamic tasks, suggesting a deficit of dorsal visual stream processing in autism. However, previous findings by Bertone et al. indicate that neuro-integrative mechanisms used to detect complex motion, rather than motion perception per se, may be impaired in autism. We present here the first demonstration of concurrent enhanced and decreased performance in autism on the same visuo-spatial static task, wherein the only factor dichotomizing performance was the neural complexity required to discriminate grating orientation. The ability of persons with autism was found to be superior for identifying the orientation of simple, luminance-defined (or first-order) gratings but inferior for complex, texture-defined (or second-order) gratings. Using a flicker contrast sensitivity task, we demonstrated that this finding is probably not due to abnormal information processing at a sub-cortical level (magnocellular and parvocellular functioning). Together, these findings are interpreted as a clear indication of altered low-level perceptual information processing in autism, and confirm that the deficits and assets observed in autistic visual perception are contingent on the complexity of the neural network required to process a given type of visual stimulus. We suggest that atypical neural connectivity, resulting in enhanced lateral inhibition, may account for both enhanced and decreased low-level information processing in autism.

Adolescent↗

Visual function assessment and metamorphopsia after macular hole surgery.

The purpose of this study was to develop a new resolution acuity measure for patients after macular hole surgery. Fifty eyes of 44 patients who had undergone successful treatment were tested. Visual acuity was measured with the Snellen, Early Treatment of Diabetic Retinopathy Study and Landolt-C charts. A Line Resolution Test was performed as part of their follow-up exam where a vertical line was presented. Participants were categorized by their perception of the line as solid, bent or broken. The line could be distorted into a sine-wave pattern in order to determine the participants' detection threshold for the distortion. Chart acuities did not differ among the three groups, as categorized by their line perception. Only the distortion measure was sensitive enough to differentiate the solid- from the broken-line group. The distortion measure assesses resolution power of the macula in smaller increments than acuity charts. This hyperacuity approach is more appropriate in the assessment of functional outcome after microsurgery.

Aged↗

Red-green chromatic mechanisms in normal aging and glaucomatous observers.

PURPOSE: This study was designed to determine whether normal aging and glaucoma are associated with red-green (R/G) chromatic processing abnormalities, a function that is primarily performed by the parvocellular visual pathway. METHODS: Chromatic processing mechanisms were examined in 98 glaucomatous observers (between the ages of 49 and 93 years; mean age, 70.8 +/- 9.4 [SD]) and 67 normal observers (between the ages of 49 and 88; mean age, 70.6 +/- 10.6 years) with the use of the minimum-motion and motion-nulling paradigms. Phakic glaucomatous (n = 60; mean age, 68.7 +/- 8.9 years) and normal (n = 32; mean age, 69.8 +/- 10.6 years) and pseudophakic glaucomatous (n = 38; mean age, 74 +/- 9.4 years) and normal (n = 35; mean age, 71.4 +/- 10.6 years) subjects were tested to evaluate the effects of lenticular aging on color perception. RESULTS: Phakic observers (normal or glaucomatous) displayed significantly different minimum-motion values than did both their younger counterparts and all the pseudophakic subjects. These results suggest that normal aging with the presence of a natural lens is accompanied by a significant decrease in green-light sensitivity, an effect that is not exacerbated by glaucoma and is primarily related to optical factors. The data also revealed no differences in color motion perception between groups, indicating that the higher cortical mechanisms of the parvocellular pathway implicated in the analysis of information about the middle and long wavelengths of the visible spectrum are not selectively affected by the disease process and normal aging. CONCLUSIONS: Normal aging and glaucoma do not produce significant R/G chromatic processing deficits at retinal and postretinal levels when optical factors are excluded. The authors propose the hypothesis that glaucoma-related effects on motion perception and blue-on-yellow perimetry should be viewed as evidence of loss of ganglion cells that necessitates integration of information over larger retinal areas and more receptor cells than in the R/G chromatic system. Ganglion cells with large receptive fields involve more neural connections and are less numerous than those that respond to R/G information. The functional consequence of this could be that the loss of a single ganglion cell with a larger receptive field would have a greater impact on visual function than the loss of a ganglion cell with a smaller receptive field, such as the ones that process R/G information. The authors believe that glaucoma-induced functional loss is best viewed as related to receptive field structure and function rather than to anatomic cell-type damage.

Aged↗

Motion perception in autism: a "complex" issue.

We present the first assessment of motion sensitivity for persons with autism and normal intelligence using motion patterns that require neural processing mechanisms of varying complexity. Compared to matched controls, our results demonstrate that the motion sensitivity of observers with autism is similar to that of nonautistic observers for different types of first-order (luminance-defined) motion stimuli, but significantly decreased for the same types of second-order (texture-defined) stimuli. The latter class of motion stimuli has been demonstrated to require additional neural computation to be processed adequately. This finding may reflect less efficient integrative functioning of the neural mechanisms that mediate visuoperceptual processing in autism. The contribution of this finding with regards to abnormal perceptual integration in autism, its effect on cognitive operations, and possible behavioral implications are discussed.

Adolescent↗

How is complex second-order motion processed?

Converging psychophysical and electrophysiological evidence suggests that first-order (luminance-defined) complex motion types i.e., radial and rotational motion, are processed by specialized extrastriate motion mechanisms. We ask whether radial and rotational second-order (texture-defined) motion patterns are processed in a similar manner. The motion sensitivity to translating, radiating and rotating motion patterns of both first-order (luminance-modulated noise) and second-order (contrast-modulated noise) were measured for patterns presented at four different exposure durations (106, 240, 500 and 750 ms). No significant difference in motion sensitivity was found across motion type for the first-order motion class across exposure duration (i.e., from 240 to 750 ms) whereas direction-identification thresholds for radiating and rotating second-order motion were significantly greater than that of the second-order translational stimuli. Furthermore, thresholds to all second-order motion stimuli increased at a significantly faster rate with decreasing exposure duration compared to those of first-order motion. Interestingly, simple and complex second-order thresholds increased at similar rates. Taken together, the results suggest that complex second-order motion is not analyzed in a sequential manner. Rather, it seems that the same 'hard-wired' mechanisms responsible for complex first-order motion processing also mediate complex second-order motion, but not before the pre-processing (i.e., rectification) of local second-order motion signals.

Adult↗

Separate neural pathways for contour and biological-motion cues in motion-defined animal shapes.

To determine whether contour and biological motion (BM) cues for motion-defined shapes are subserved by two separate mechanisms, we used PET to measure regional cerebral blood flow in nine human subjects. Subjects were scanned in the following four conditions: (1) contour-defined animals with natural movements (running), (2) motion-defined animals in which the contours were removed and dots were placed on the limbs and moving parts (BM; running); (3) drifting static animal shapes (contours); and (4) drifting dots. The results demonstrate that the perception of BM involves the superior frontal gyrus, the precuneus, the fusiform, the lingual and the medial temporal gyri, the inferior parietal lobe, the hippocampal and parahippocampal areas, and the cerebellum. In addition, the anterior cingulate cortex and the amygdala were significantly activated. The perception of contour-defined shapes produced significant elevation of rCBF in some areas similar to the BM condition, namely the fusiform, medial occipital, medial temporal, and lingual gyri. Only the occipital pole and the inferior temporal cortex were specifically activated by contour-defined shapes. These results are congruent with previous findings that the dorsal visual pathway is important for the perception of BM. They further support psychophysical results showing that contour and BM cues for motion-defined animal shapes are processed by independent channels.

Adult↗

The fluttering-heart illusion: a new hypothesis.

The fluttering-heart illusion is a perceived lagging behind of a colour target on a background of a different colour when the two are oscillated together. It has been proposed that the illusion is caused by a differential in the perceptual latencies of different colours (Helmholtz 1867/1962), a differential in rod-cone latencies (von Kries 1896) and rod-cone interactions (von Grünau 1975, 1976 Vision Research 15 431-436, 437-440; 16 397-401; see list of references there). The purpose of this experiment was to assess the hypothesis that the fluttering-heart illusion is caused by a differential in the perceived velocities of chromatic and achromatic motion. To evaluate this hypothesis, we tested observers possessing normal colour vision and deuteranopes. The perceived delay of a chromatic target relative to an achromatic target was measured as a function of background cone contrast and target colour. For observers with normal colour vision, the perceived delay of the chromatic target is greater in the L-S than the L-M testing conditions. The reverse is observed in deuteranope observers. We suggest that this is caused by the absence of an L-M opponent mechanism contributing to chromatic motion in deuteranopes. Greater background cone contrasts tended to yield smaller perceived delays in both normal and deuteranope observers, indicating that greater chromatic modulation decreases the perceived delay of the colour target. These results support the hypothesis that the fluttering-heart illusion can be explained by a differential in the perceived velocities of chromatic and achromatic motion.

Color Perception↗

The role of lenticular senescence in age-related color vision changes.

PURPOSE: It has been reported that greater age-related losses in sensitivity occur for short-wavelength visual stimuli than for medium- and long-wavelength visual stimuli. The purpose of the current experiment was to determine to what extent optical, receptoral, and postreceptoral factors contribute to these age-related changes in color vision. METHODS: One hundred two observers (ages 18-87) completed a minimum motion task to determine isoluminance between red and green and between red and blue. A motion-nulling task was also performed to assess the L-M postreceptoral chromatic mechanism. RESULTS: No significant age-related changes occurred in red-green isoluminance values. Red-blue isoluminance values showed a significant and systematic decrease with age in observers with phakic eyes. Pseudophakic eyes in older subjects performed this task as well as phakic eyes in young subjects. The motion-nulling results demonstrated small age-related losses in the postreceptoral color mechanisms. CONCLUSIONS: The findings of this experiment, particularly those of the red-blue isoluminance task, indicate that the optical factor of lenticular senescence is the main contributor to the age-related changes observed in color vision. A model based on age-related changes in lenticular absorbance shows good fit with the experimental data of observers with phakic eyes, suggesting that optical factors are the main cause of the age-related changes in these color vision tasks.

Adolescent↗

Configural face encoding and spatial frequency information.

Configural relations and a critical band of spatial frequencies (SFs) in the middle range are particularly important for face recognition. We report the results of four experiments in which the relationship between these two types of information was examined. In Experiments 1, 2A, and 2B, the face inversion effect (FIE) was used to probe configural face encoding. Recognition of upright and inverted faces and nonface objects was measured in four conditions: a no-filter condition and three SF conditions (low, medium, and high frequency). We found significant FIEs of comparable magnitudes for all frequency conditions. In Experiment 3, discrimination of faces on the basis of either configural or featural modifications was measured under the same four conditions. Although the ability to discriminate configural modifications was superior in the medium-frequency condition, so was the ability to discriminate featural modifications. We conclude that the band of SF that is critical for face recognition does not contribute preferentially to configural encoding.

Adolescent↗

Cortical areas mediating stereopsis in the human brain: a PET study.

Using PET, we investigated the neural substrates of stereodepth perception in humans. The presentation of Julesz-type random-dot stereograms (RDS) produced significant rCBF elevations in Brodmann areas (BA) 18, 19 and 7, all in the right hemisphere. Activation foci were also found in both middle temporal areas (MT). These results demonstrate that, as in primates, cortical area MT and extrastriate areas are central to stereovision and that a network of predominant right hemispheric regions is recruited to meet visuo-spatial processing demands associated with horizontal binocular disparity inputs.

Adult↗