Neural Mechanisms of Visual Crowding
Neural Mechanisms of Visual Crowding
批准号:
7467651
负责人:
BRAD C MOTTER
金额:
$37.63万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-04-01 至 2012-03-31
关键词:
AffectAge related macular degenerationAlzheimer&aposs DiseaseAreaAttentionAutomobile DrivingBiological ModelsBlurClinicalCognitiveConditionConstriction procedureCrowdingDailyDiscriminationDiseaseEvaluationEyeGoalsGrantHeadHealthImageLeadLettersMacular degenerationMapsMeasuresMethodsNeuronsOcular FixationPeripheralPlayPrintingPsychophysiologyPublic HealthRangeRateReadingRehabilitation therapyResearchResponse to stimulus physiologyRoleSensoryStandards of Weights and MeasuresStimulusTechniquesThinkingV4 neuronVisionVision DisordersVisualVisual FieldsVisual PerceptionVisual impairmentVisuospatialWorkaging populationarea V4area striatabaseexperienceextrastriateextrastriate visual corteximpressionimprovedneuromechanismneurophysiologynormal agingprogramsreceptive fieldrelating to nervous systemresearch studyresponseretinotopicsample fixationsizevisual receptive fieldvisual searchvisual stimulus
中文摘要
描述(由申请人提供):我们的目标是了解视觉拥挤的神经机制。拥挤是一种刺激相互作用的现象,导致视觉感知的模糊退化。在不移动眼睛的情况下,只有一小部分视觉场景会产生清晰的视觉体验。这个区域被称为功能性视野。在其中,我们可以选择和仔细检查项目,识别和定义它们的特征和相互关联的部分。在它之外,我们很难对周围的物体形成清晰、生动的印象。我们的假设是,跨越功能性视野边界的过渡是由视觉空间拥挤控制的。拥挤在限制中心视野丧失(如黄斑变性)患者的剩余视觉功能方面起着重要作用,因为它极大地限制了外围视野在日常活动(如阅读)中的使用。中央视野丧失导致的视力低下的人阅读速度特别慢,因为近外围的拥挤占主导地位。我们研究的一个目标是了解拥挤是如何从神经元接受区的信息聚合中产生的。
英文摘要
DESCRIPTION (provided by applicant): Our goal is to understand the neural mechanisms of visual crowding. Crowding is a stimulus interaction phenomenon that results in a blurring degradation of visual perception. Without moving the eyes only a small area of the visual scene gives rise to a clear visual experience. This area is known as the functional visual field. Within it we can select and scrutinize items, recognize and define their features and interrelated parts. Outside of it we have difficultly forming distinct, vivid impressions of the objects surrounding us. Our hypothesis is that the transition across the functional visual field boundary is governed by visual spatial crowding. Crowding plays a major role in limiting the remaining visual function of people with central visual field loss, e.g., macular degeneration, because it dramatically limits the use of the peripheral visual field for daily activities such as reading. Reading is especially slow for people with low vision from central field loss because of the dominance of crowding in the near periphery. A goal of our research is to understand how crowding results from the convergence of information in neuronal receptive fields.
We have identified extrastriate cortical area V4 as an area likely to be involved in the interactions of letter-like visual stimuli that lead to crowding phenomena. The proposed research examines five principle questions about the neural mechanisms of crowding. 1) Are the spatial asymmetries of crowding explained by the neural rescaling of spatial information known as the cortical magnification factor? 2) Does organization with respect to the center of the receptive field play a critical role in determining crowding interactions at the neuronal level? 3) Does stimulus size play a major role in crowding within the receptive field or is the primary factor spacing? 4) Does attention alter crowding by changing the basic sensitivity within the crowded area or is it needed to readout information without altering the basic sensitivity? 5) Are the influences of the suppression surround critical in modulating the crowding interactions within the classic receptive field? These issues will be investigated using neurophysiological techniques to study the activity of single cortical neurons while subjects perform visual fixation and visual attentive discrimination tasks.
PUBLIC HEALTH RELEVANCE: Millions of people now suffer from low vision disorders that limit central vision; these disorders increase within the aging population. The goal of this research program is to provide an understanding of the neural mechanisms of visual crowding that limit the use of the peripheral vision in normal daily activities such as reading and driving. Understanding of the basic neural mechanism can lead to enhanced clinical approaches, suggest alternate rehabilitative methods, and provide for better, more precise evaluations of visual health.
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Neural Mechanisms of Visual Crowding
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批准号:7587255
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项目类别:
-
资助金额:$37.63万
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财政年份:2008
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负责人:BRAD C MOTTER
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依托单位:
Neural Mechanisms of Visual Crowding
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批准号:8066335
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项目类别:
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资助金额:$35.76万
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财政年份:2008
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负责人:BRAD C MOTTER
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依托单位:
Neural Mechanisms of Visual Crowding
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批准号:7796661
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项目类别:
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资助金额:$37.25万
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财政年份:2008
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负责人:BRAD C MOTTER
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依托单位:
VISUAL ATTENTIVE PROCESSES
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批准号:3263925
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项目类别:
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资助金额:$9.76万
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财政年份:1986
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负责人:BRAD C MOTTER
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依托单位:
VISUAL ATTENTIVE PROCESSES
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批准号:3263922
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项目类别:
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资助金额:$8.13万
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财政年份:1986
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负责人:BRAD C MOTTER
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依托单位:
VISUAL ATTENTIVE PROCESSES
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批准号:2161243
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项目类别:
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资助金额:$10.78万
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财政年份:1986
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负责人:BRAD C MOTTER
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依托单位:
VISUAL ATTENTIVE PROCESSES
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批准号:3263926
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项目类别:
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资助金额:$10.04万
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财政年份:1986
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负责人:BRAD C MOTTER
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依托单位:
VISUAL ATTENTIVE PROCESSES
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批准号:3263924
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项目类别:
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资助金额:$8.0万
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财政年份:1986
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负责人:BRAD C MOTTER
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依托单位:
VISUAL ATTENTIVE PROCESSES
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批准号:3263923
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项目类别:
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资助金额:$5.28万
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财政年份:1986
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负责人:BRAD C MOTTER
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依托单位:
VISUAL ATTENTIVE PROCESSES
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批准号:3263921
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项目类别:
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资助金额:$9.58万
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财政年份:1986
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负责人:BRAD C MOTTER
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依托单位:
VISUAL ATTENTIVE PROCESSES
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批准号:3263919
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项目类别:
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资助金额:$8.39万
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财政年份:1986
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负责人:BRAD C MOTTER
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依托单位:
ATTENTIONAL CONTROL OF VISUAL PROCESSES
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批准号:3930134
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:BRAD C MOTTER
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依托单位:
ATTENTIONAL CONTROL OF VISUAL PROCESSES
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批准号:3909006
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:BRAD C MOTTER
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依托单位:
ATTENTIONAL CONTROL OF VISUAL PROCESSES
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批准号:3952786
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:BRAD C MOTTER
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依托单位:
海外基金