February 2022
Volume 22, Issue 3
Open Access
Optica Fall Vision Meeting Abstract  |   February 2022
Invited Session II: Retinal mechanisms mediating vision: Light adaptation in primate fovea
Author Affiliations
  • Raunak Sinha
    Dept. of Neuroscience, University of Wisconsin, USA
Journal of Vision February 2022, Vol.22, 44. doi:https://doi.org/10.1167/jov.22.3.44
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      Raunak Sinha; Invited Session II: Retinal mechanisms mediating vision: Light adaptation in primate fovea. Journal of Vision 2022;22(3):44. https://doi.org/10.1167/jov.22.3.44.

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      © ARVO (1962-2015); The Authors (2016-present)

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Our visual performance varies remarkably across space. For instance, our central vision exhibits the highest spatial and chromatic sensitivity, whereas temporal sensitivity is higher for our peripheral than central vision. Our high-acuity central vision is initiated in the cone photoreceptors which are packed in a dense array in the fovea. The density and morphology of cones differ remarkably between foveal and peripheral primate retina, but our knowledge about their functional differences remain quite poor. In the past we have shown that cone signals in the fovea are two-fold slower than in the peripheral retina consistent with the difference in the temporal sensitivity of cone-mediated vision to high-frequency flicker. But we are far from understanding the full breadth of these topographic differences in cone signaling across primate retina over a wide range of light inputs. I will present recent results of a detailed comparison of functional properties - such as kinetics, gain and cellular noise - of cones in the fovea with that in rest of the primate retina. I will show how foveal cones adapt across a wide range of lumice and if they exhibit differences in the amplitude, kinetics or timescales of adaptation when compared to cones in the peripheral primate retina. Lastly, I will share our findings on the relative contribution of cone vs circuit mechanisms towards lumice adaptation in the domit neural circuit in the fovea - the midget ganglion cell pathway.

 Funding: NIH grants (EY026070, EY031411), BrightFocus Foundation, McPherson Eye Research Institute,

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