Thesis (M.A.)--York University, 2008. Graduate Programme in Psychology. / Typescript. Includes bibliographical references (leaves72-76). Also available on the Internet. MODE OF ACCESS via web browser by entering the following URL: http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:MR45969

Visual search can simply be defined as the task of looking for an object of interest in a visual environment. Due to its foveated nature, the human visual system succeeds at such task by making many discrete fixations linked by rapid eye movements called saccades. However, very little is known about how saccadic targets (fixation loci) are selected by the brain in such naturalistic tasks. Discoveries to be made are not only invaluable to the field of vision science but are very important in designing automated vision systems, which to this day lag in performance vis-à-vis human observers. What I have sought to accomplish in this dissertation has been to reveal previously unknown saccadic targeting and target selection strategies used by human observers in naturalistic visual search tasks. My driving goal has been to understand how the brain selects fixation loci and target candidates upon fixation, with the objective of using these findings for automated fixation selection algorithms employed for visual search. I have proposed a novel and efficient technique akin to psychophysical reverse correlation to study human observer strategies in locating low-contrast targets under a variety of experimental conditions. My technique has successfully been used to study saccadic programming and target selection in various experimental conditions, including visual searches for targets with known characteristics, targets whose orientation attributes are not known a priori, and targets containing multiple orientations. I have found visual guidance in saccadic targeting and target selection under all experimental conditions, revealed by observers' selectivity for spatial frequencies and/or orientations of stimuli close to that of the target. I have shown that under uncertainty, observers rely on known target characteristics to direct their saccades and to select target candidates upon foveal scrutiny. Moreover, I have demonstrated that multiple orientation characteristics of targets are represented in observer search strategies, modulated by their sensitivity / selectivity for each orientation. Some of my findings have been applied towards applications for automated visual search algorithms.

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In this dissertation, we study the relationship between eye movements and visual attention. Different types of eye movements are investigated including microsaccades, eye fixation, and eye pursuit. First, we demonstrate that microsaccades occur during pursuit and they are linked to covert attention shifts. Employing a psychophysical task that involves covert attention shifts to a peripheral square, we detect if microsaccades occur during eye pursuit, and, if so, whether, and in what way, microsaccades are related to attention shifts. Microsaccades are found to occur during pursuit and they present in similar patterns as those occurring during eye fixation. We discover that microsaccades tend to be biased towards the same direction as pursuit and the bias increases with increases of pursuit velocities. Through the analysis of microsaccade orientation and latency, we argue that microsaccades occurring during pursuit, rather than being randomly distributed, have a link with covert attention shifts. This is consistent with what has been reported for microsaccades occurring during fixation. Further analysis of microsaccade amplitude supports this argument. The potential attention mechanisms for the characteristics of microsaccades are discussed. We suggest that the attention allocation during pursuit is responsible for the characteristics of microsaccades. Our analyses of microsaccades also enforce the argument that microsaccades may be the suppressed saccades. / In addition to microsaccades, the attention allocation during eye fixation and eye pursuit are considered as well. We demonstrate that, during eye fixation, the local image content around the area of a fixation point is a significant factor to influence the fixation duration. However, during pursuit, the pursuit direction, rather than image contents, is important to decide attention allocation. According to these results, a top-down attention model based on types of eye movements is built. Three types of eye movements are considered separately in the model. They are eye fixation, eye pursuit, and saccadic eye movements (including microsaccades). The model is applied to the design of an interactive 2D video game. We demonstrate that the game is successfully designed in different difficulty levels through the analysis of attention allocation by our attention model. Our results imply that the attention modeling can be used to alter the game play so as to provide varying difficulty levels and it is also promising to take advantage of eye tracking data for broader applications, such as for navigation, intelligent map searching, augmented reality, and others.

We have a strong intuition that people's eyes are unique, socially informative stimuli. As such, it is reasonable to propose that humans have developed a fundamental tendency to preferentially attend to eyes in the environment. The empirical evidence to support this intuition is, however, remarkably thin. Over the course of eight chapters, the present thesis considers the area of social attention, and what special role (if any) the selection of eyes has in it. Chapters 2 and 3 demonstrate that when observers are shown complex natural scenes, they look at the eyes more frequently than any other region. This selection preference is enhanced when the social content and activity in the scene is high, and when the task is to report on the attentional states in the scene. Chapters 4 and 5 establish that the bias to select eyes extends to a variety of tasks, suggesting that it may be fundamental to human social attention. In addition, Chapter 5 shows that observers who are told that they will have to remember the scenes look more often at the eyes than observers who are unaware of the forthcoming memory test; moreover this difference between groups persists to scene recognition. Chapter 6 examines whether the preference for eyes can be explained by visual saliency. It cannot. Chapter 7 compares the selection of eyes to another socially communicative cue, the arrow. The results shed light on a recent controversy in the social attention field, and indicate again that there is a fundamental bias to select the eyes. Collectively the data suggest that for typically developing adults, eyes are rich, socially communicative stimuli that are preferentially attended to relative to other stimuli in the environment.

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The primary focus of this research was to examine that portion of the model for psychotherapy developed by John Grinder and Richard Bandler in their 1976 book, The Structure of Magic II, concerned with internal representational systems. Specifically, the study was designed to investigate the relationship between reflexive eye movement patterns, verbalizations, and individual self-report as measures of representational systems. This comparison was made to determine if the three variables would demonstrate significant agreement as predictors of internal representational systems.Students in undergraduate psychology courses in two different departments of a large midwestern university were solicited as subjects for this research. One hundred and twenty-eight individuals participated in the study. Those individuals who participated represented various age groups and academic majors. In this study subjects served as their own controls.Four hypotheses were formulated to investigate the probability of various combinations of eye movements, verbalizations, and individual self-reports as predictors of respresentational systems. The author developed nine stimulus cues for subject response. Six cues required no verbal response and were used for eye movement rating only. The remaining three cues were responded to verbally and provided both eye movement and verbalization ratings. Each subject was individually rated on eye movements and verbalizations by different raters. A frequency count procedure was utilized in rating each individual's eye movements and verbalizations. The most frequently occurring system was classified as the primary representational system for each of these variables. At the completion of the study, each individual provided information on his or her primary representational system through use of a short questionnaire developed by the author. The representational system rated as number one on the self-report questionnaire was classified as the primary representational system for individual self-report. The results of all ratings were classified as either visual, kinesthetic, or auditory and then compared on the variables.Statistical analyses were carried out to determine if there was significant agreement (p<.05) between the variables. Analysis of the results indicated one significant finding. The most reliable means of determining representational systems in this study was through a combination of observing eye movements and listening to the predicate system most frequently used in the verbalizations of an individual. This method was more reliable than observing eye movements and obtaining an individual's self-report; or listening to the most frequently used predicate system and obtaining an individual's self-report; or observing eye movements, listening for the most frequently used predicate system, and obtaining an individual's self-report. The combination of observing eye movements and listening for the most frequently used predicate system was statistically significant. All other combinations mentioned failed to reach statistical significance.

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Purpose: To test the hypothesis that the fixational stability (FS) of the amblyopic eye (AME) in strabismics will improve when binocular integration is enhanced through ocular alignment and inter-ocular suppression is attenuated by reducing the contrast to the fellow eye (FFE). Methods: 7 strabismic amblyopes (age: 30.8±9.7 yrs) (5 esotropes and 2 exotrope) (VA: AME=0.50±0.30; FFE=-0.12±0.04) showing clinical characteristics of central suppression were recruited. Suppression was then attenuated by a balance point procedure where the contrast to the FFE was reduced in order to maximize binocular integration during a global motion task (GMT) (Baker, 2007). In one case the balance point could not be determined, and the participant was excluded. Ocular alignment was established with a haploscope. Participants dichoptically viewed similar targets [a cross (2.3°) surrounded by a square (11.3°) visual angle] set at 40cm. Target contrasts presented to each eye were either equal (EQ) or attenuated in the FFE (UNEQ) by an amount defined by the GMT. FS was measured over a 5 min period (Viewpoint® Eye Tracker, Arrington Research) and quantified using bivariate contour ellipse areas (BCEA) in four different binocular conditions; unaligned/EQ, unaligned/UNEQ, aligned/EQ and aligned/UNEQ. FS was also measured in 6 control subjects (Age: 25.3±4 yrs; VA: -0.1±0.08). Results: Alignment of the AME was transient and lasting between 30 to 80 seconds. Accordingly, FS was analyzed over the first 30 seconds using repeated measures ANOVA. Post hoc analysis revealed that for the amblyopic subjects, the FS of the AME was significantly improved in aligned/EQ (p=0.015) and aligned/UNEQ (p=0.001). FS of FFE was not different statistically across conditions. BCEA(FFE) & BCEA(AME) were then averaged for each amblyope in the 4 conditions and compared with normals. This averaged BCEA (reduced FS) was significantly greater (p=0.0205) in amblyopes compared to controls except in the case of alignment coupled with reduced suppression (aligned/UNEQ) (p=0.1232). Conclusion: Fixation stability in the amblyopic eye of strabismics appears to improve directly with the degree of binocular integration. The hypothesis is therefore retained.