Probing Computation in the Primate Visual System at Single-Cone Resolution.
Abstract
Daylight vision begins when light activates cone photoreceptors in the retina, creating
spatial patterns of neural activity. These cone signals are then combined and processed
in downstream neural circuits, ultimately producing visual perception. Recent technical
advances have made it possible to deliver visual stimuli to the retina that probe
this processing by the visual system at its elementary resolution of individual cones.
Physiological recordings from nonhuman primate retinas reveal the spatial organization
of cone signals in retinal ganglion cells, including how signals from cones of different
types are combined to support both spatial and color vision. Psychophysical experiments
with human subjects characterize the visual sensations evoked by stimulating a single
cone, including the perception of color. Future combined physiological and psychophysical
experiments focusing on probing the elementary visual inputs are likely to clarify
how neural processing generates our perception of the visual world. Expected final
online publication date for the Annual Review of Neuroscience Volume 42 is July 8,
2019. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
Type
Journal articlePermalink
https://hdl.handle.net/10161/18195Published Version (Please cite this version)
10.1146/annurev-neuro-070918-050233Publication Info
Kling, A; Field, GD; Brainard, DH; & Chichilnisky, EJ (2019). Probing Computation in the Primate Visual System at Single-Cone Resolution. Annual review of neuroscience, 42(1). 10.1146/annurev-neuro-070918-050233. Retrieved from https://hdl.handle.net/10161/18195.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Greg D. Field
Adjunct Associate Professor of Neurobiology
My laboratory studies how the retina processes visual scenes and transmits this information
to the brain. We use multi-electrode arrays to record the activity of hundreds of
retina neurons simultaneously in conjunction with transgenic mouse lines and chemogenetics
to manipulate neural circuit function. We are interested in three major areas. First,
we work to understand how neurons in the retina are functionally connected. Second
we are studying how light-adaptation and circadian rhythms a

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