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Visual images from the two eyes are transmitted to the brain. Because the eyes are horizontally separated, there is a horizontal disparity between the two images. The amount of disparity between the images of a given point depends on the distance of that point from the viewer's point of fixation. A natural visual environment contains surfaces at many different depths. Therefore, the brain must process a spatial distribution of disparities. How are these disparities spatially put together? Brief (about 200 msec) static Cyclopean random-dot stereograms were used as stimuli for vergence and depth discrimination to answer this question. The results indicated a large averaging region for vergence, and a smaller pooling region for depth discrimination. Vergence responded to the mean disparity of two transparent planes. When a disparate target was present in a fixation plane surround, vergence improved as target size was increased, with a saturation at 3-6 degrees. Depth discrimination thresholds improved with target size, reaching a minimum at 1-3 degrees, but increased for larger targets. Depth discrimination showed a dependence on the extent of a disparity pedestal surrounding the target, consistent with vergence facilitation. Vergence might, therefore, implement a coarse-to-fine reduction in binocular matching noise. Interocular decorrelation can be considered as multiple chance matches at different disparities. The spatial pooling limits found for disparity were replicated when interocular decorrelation was discriminated. The disparity of the random dots also influenced the apparent horizontal. alignment of neighbouring monocular lines. This finding suggests that disparity averaging takes place at an early stage of visual processing. The following possible explanations were considered: 1) Disparities are detected in different spatial frequency channels (Marr and Poggio, 1979). 2) Second-order luminance patterns are matched between the two eyes using non-linear channels. 3) Secondary disparity filters process disparities extracted from linear filters.

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L’objectif de ce travail de thèse était d’étudier l’implication des systèmes visuels magnocellulaire et parvocellulaire dans le traitement de langage écrit, spécialement dans l’identification des mots. Quatre études expérimentales ont été réalisées afin de documenter le rôle respectif de ces deux systèmes pour différentes composantes de la structure du mot écrit, la lettre (Etude 1), la longueur du mot (Etude 2) et l’enveloppe du mot (Etude 3), ainsi que le voisinage orthographique (Etude 4). La dissociation des deux sous-systèmes visuels se fondait sur leurs caractéristiques fonctionnelles spécifiques : sensibilité aux fréquences spatiales basses et au contraste de luminance pour le système magnocellulaire ; sensibilité aux fréquences spatiales moyennes et élevées et au contraste chromatique pour le système parvocellulaire. Les participants étaient des adultes jeunes normolecteurs et des enfants de 10-11 ans, lecteurs novices, afin d’envisager l’implication de chaque système visuel à deux étapes de leur développement : maturité chez l’adulte jeune ; en cours de maturation chez l’enfant. Les résultats ont confirmé le rôle prépondérant des traitements parvocellulaires, ce qui corroborait le privilège accordé au traitement des lettres et traits des lettres dans la reconnaissance visuelle des mots. Le traitement de la longueur du mot s’est en revanche révélé être une dimension sélectivement magnocellulaire. L’ensemble des résultats est discuté dans le cadre de l’approche coarse-to-fine. / The main objective was to study the implication of the magnocellular and the parvocellular visual systems in written language processing, specifically in word identification. Four studies were carried out to document the respective roles of these two systems, for different components of the written word structure, the letter (Study 1), the word length (Study 2), the word shape (Study 3) and the orthographic neighborhood (Study 4). The dissociation of the two visual systems was based on their specific functional characteristics: sensitivity to low spatial frequencies and luminance contrast for the magnocellular system; and sensitivity to medium and high spatial frequencies and chromatic contrast for the parvocellular system. The participants were young adult normal readers and 10-11 years-old children, novice readers, in order to consider the involvement of each visual system at two stages of their development: mature in young adults while still maturing in the children. The results confirmed the prominent role of parvocellular processing, which was consistent with the privilege accorded to the processing of letters and letters features in visual word recognition. On the other hand, word length processing has been shown to be a selectively magnocellular dimension. All results are discussed in the framework of the coarse-to-fine approach.

Face perception is impaired in a variety of ways in older adults, but the mechanisms underlying these changes remain unclear. A central theme of this dissertation is that task performance is constrained by two factors intrinsic to the observer: sources of random variability -- internal noise -- and the efficiency with which task-relevant stimulus information is utilized. This thesis uses several behavioural, psychophysical methods to examine how age-related changes in one or both of these factors affect face processing. Chapter 2 used the classification image (CI) method to characterize the spatial sampling patterns of younger and older observers performing a face discrimination task. Compared to younger adults, older adults used information in the eye/brow region less consistently and instead relied on relatively less informative regions such as the forehead. The differences in CIs accounted for the lower absolute efficiency that was found in older observers. Chapter 3 estimated internal noise and calculation efficiency by measuring threshold-vs.-noise (TvN) curves and response consistency in a face discrimination task. Compared to younger observers, older observers had higher additive internal noise and lower calculation efficiency, but the magnitude of multiplicative internal noise did not differ between age groups. Previous studies have shown that younger adults have a bias to rely on horizontal structure to discriminate and identify faces, and the magnitude of this so-called horizontal bias is correlated with identification accuracy. The experiments in Chapter 4 measured horizontal bias in younger and older adults, and found that age differences in horizontal bias account for some, but not all, of the age difference in face identification accuracy. In summary, my work demonstrates that additive (but not multiplicative) internal noise is greater in older adults, and that they are less efficient at sampling information that is conveyed by structure at different locations and orientations in a face. / Dissertation / Doctor of Science (PhD) / Our experience of the visual environment results from perceptual processes in the brain. Many of these processes change with age, such as our ability to identify someone from a photograph of their face. Performance is influenced by both random variability, or "noise", within the observer and how efficiently we use task-relevant information in the visual environment. By systematically manipulating the amount of available stimulus information I assessed the contribution of these factors to older adults' judgements of facial identity, and characterized the information on which these decisions are based. These experiments are the first to consider how face perception in older adults is constrained by the combined effects of internal noise and the efficiency with which the visual system utilizes various sources of information. The results provide a number of directions for future research in the fields of face perception and age-related changes in complex pattern vision.