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At and beyond the neural limits: visual psychophysics using an adaptive-optics visual stimulator

At and beyond the neural limits: visual psychophysics using an adaptive-optics visual stimulator
达到和超越神经极限:使用自适应光学视觉刺激器的视觉心理物理学
批准号:
BB/M01858X/1
负责人:
Andrew Stockman
金额:
$63.9万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2015
资助国家:
英国
项目状态:
已结题
起止时间:
2015 至 --

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中文摘要
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英文摘要
The optics of all of our eyes are to some degree imperfect, even those of individuals with "20/20 vision". These imperfection produce small, often imperceptible, aberrations in the images that we see and limits both image quality and visual acuity.New technology first developed for astronomy, called "adaptive optics" or AO for short, can correct those aberrations and produce nearly perfect, aberration-free images in the eye. Most AO relies on the use of a flexible mirror that can be deformed in a controlled away. The optical aberrations present in the eye are measured and the inverse of those distortions are applied to the mirror, thus correcting the image quality and overcoming the optical aberrations that usually limit image quality in the eye.AO instruments can be used in two ways in visual science: either to look into the eye or to look out of it. Looking into the eye, instruments that image the retina at the back of the eye can be improved by AO to the extent that individual cells can be resolved. Looking out of the eye, the resolution of a visual image projected onto to retina can be increased by AO to beyond normal visual acuity, producing so called "super-vision". The instrument that we will design and build will be a user-friendly AO visual stimulator with which we can do both of these things. The device will include a digital light projector-normally used to project images in cinemas-that will project super high resolution images directly onto the retina. The primary purpose of the instrument is to investigate the underlying properties of the eye and brain beyond the normal limits imposed by the optics of the eye. Experiments will be conducted to test how well observer are able to see by asking them to make judgments about what they can see. Once the device is constructed, we will embark on a series of standard measurements of human visual performance. Rather than trying to measure the response to complex visual scenes, we will measure an observer's sensitivity to simple spatial patterns made up of periodic patterns of light and dark. These simple "sinusoidal" patterns are the building blocks from which we can predict the responses to any complex stimuli. To fully characterise the vast space of possible visual scenes, the simple sinusoidal patterns will be systematically varied from coarse to fine. For each pattern, we will determine how much contrast the observer needs to just see the pattern. From these measurements, we derive the spatial contrast sensitivity function (or spatial CSF) that defines the visual performance of the human observer. The importance of the AO system is that we can use it to measure spatial CSFs without the measurements being limited by the optics of the eye. Moreover, we can make those measurements for chromatic stimuli, achromatic stimuli and stimuli detected by single classes of light-sensitive detectors. By using different stimuli, we can investigate different neural pathways in the visual system.The AO stimulator will also allow us to investigate human vision beyond the usual neural limits of the system. Visual patterns produced by the AO stimulator that are too fine to be seen directly (and are therefore "invisible") can be seen indirectly due to interactions between pairs of patterns or due to changes in apparent intensity when a pattern is turned on and off. Using these patterns we will be able to investigate the underlying properties of the neurons in the visual system. Again, we can make measurements using chromatic stimuli, achromatic stimuli and stimuli detected by single classes of light-sensitive detectors. The indirect detection of these "invisible" patterns allows us to probe the inner working of the pathways answer specific questions about how the retina works.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
Hue shifts produced by temporal asymmetries in chromatic signals.
由色度信号的时间不对称性产生的色调偏移。
DOI: 10.1167/17.9.2
发表时间: 2017
期刊: Journal of vision
影响因子: 1.8
作者: [Stockman A]
通讯作者: Stockman A
Linear-nonlinear models of the red-green chromatic pathway.
红绿通道的线性非线性模型。
DOI: 10.1167/17.13.7
发表时间: 2017
期刊: Journal of vision
影响因子: 1.8
作者: [Stockman A]
通讯作者: Stockman A
DOI: 10.1073/pnas.1717356115
发表时间: 2018-04-24
期刊: Proceedings of the National Academy of Sciences of the United States of America
影响因子: 11.1
作者: [Rider AT, Henning GB, Eskew RT Jr, Stockman A]
通讯作者: Stockman A
Hue shifts produced by temporal asymmetries in chromatic signals depend on the alignment of the first and second harmonics.
由色度信号中的时间不对称性产生的色调偏移取决于一次和二次谐波的对齐。
DOI: 10.1167/17.9.3
发表时间: 2017
期刊: Journal of vision
影响因子: 1.8
作者: [Stockman A]
通讯作者: Stockman A
9
    The early human visual system laid bare by novel techniques and models: psychophysical dissection using complex flicker
    • 批准号:
      BB/R019487/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $57.57万
    • 财政年份:
      2018
    • 负责人:
      Andrew Stockman
    • 依托单位:
    Multiple signals interact in flicker: recursive surround networks
    • 批准号:
      BB/M00211X/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $53.04万
    • 财政年份:
      2014
    • 负责人:
      Andrew Stockman
    • 依托单位:
    Rank based spectral estimation
    • 批准号:
      EP/J005193/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $7.3万
    • 财政年份:
      2012
    • 负责人:
      Andrew Stockman
    • 依托单位:
    Does the sluggishness of colour perception reflect a limitation in the maximum (slew) rate at which chromatic pathways respond to changes in colour?
    • 批准号:
      BB/I003444/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $52.9万
    • 财政年份:
      2011
    • 负责人:
      Andrew Stockman
    • 依托单位:
    国内基金
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    • 批准号:
      82371631
    • 项目类别:
      面上项目
    • 资助金额:
      49.00万元
    • 批准年份:
      2023
    • 负责人:
      卢慕峻
    • 依托单位:
    亚低温调控颅脑创伤急性期神经干细胞Mpc2/Lactate/H3K9lac通路促进神经修复的研究
    • 批准号:
      82371379
    • 项目类别:
      面上项目
    • 资助金额:
      49.00万元
    • 批准年份:
      2023
    • 负责人:
      冯军峰
    • 依托单位:
    基于再生运动神经路径优化Agrin作用促进损伤神经靶向投射的功能研究
    • 批准号:
      82371373
    • 项目类别:
      面上项目
    • 资助金额:
      49.00万元
    • 批准年份:
      2023
    • 负责人:
      沃雁
    • 依托单位:
    Neural Process模型的多样化高保真技术研究