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Detection and discrimination of achromatic contrast: A ganglion cell perspective

The magnocellular (MC) pathway in the primate has much higher achromatic contrast sensitivity than the parvocellular (PC) pathway, and is implicated in luminance contrast detection. But MC pathway responses tend to saturate at lower achromatic contrast than do PC pathway responses. It has been propo...

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Detalles Bibliográficos
Autores principales: Lee, Barry B., Swanson, William H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308016/
https://www.ncbi.nlm.nih.gov/pubmed/35848903
http://dx.doi.org/10.1167/jov.22.8.11
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author Lee, Barry B.
Swanson, William H.
author_facet Lee, Barry B.
Swanson, William H.
author_sort Lee, Barry B.
collection PubMed
description The magnocellular (MC) pathway in the primate has much higher achromatic contrast sensitivity than the parvocellular (PC) pathway, and is implicated in luminance contrast detection. But MC pathway responses tend to saturate at lower achromatic contrast than do PC pathway responses. It has been proposed that the PC pathway plays a major role in discriminating suprathreshold achromatic contrast, because the MC pathway is in saturation. This has been termed the pulsed-pedestal protocol. To test this hypothesis, responses of MC and PC pathway ganglion cells have been examined under suprathreshold conditions with stimulus configurations similar to those in psychophysical tests. For MC cells, response saturation was much less for flashed or moving edges than for sinusoidal modulation, and MC cell thresholds predicted for these stimuli were similar to psychophysical discrimination (and detection) data. Results suggest the protocol is not effective in segregating MC and PC function.
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spelling pubmed-93080162022-07-24 Detection and discrimination of achromatic contrast: A ganglion cell perspective Lee, Barry B. Swanson, William H. J Vis Article The magnocellular (MC) pathway in the primate has much higher achromatic contrast sensitivity than the parvocellular (PC) pathway, and is implicated in luminance contrast detection. But MC pathway responses tend to saturate at lower achromatic contrast than do PC pathway responses. It has been proposed that the PC pathway plays a major role in discriminating suprathreshold achromatic contrast, because the MC pathway is in saturation. This has been termed the pulsed-pedestal protocol. To test this hypothesis, responses of MC and PC pathway ganglion cells have been examined under suprathreshold conditions with stimulus configurations similar to those in psychophysical tests. For MC cells, response saturation was much less for flashed or moving edges than for sinusoidal modulation, and MC cell thresholds predicted for these stimuli were similar to psychophysical discrimination (and detection) data. Results suggest the protocol is not effective in segregating MC and PC function. The Association for Research in Vision and Ophthalmology 2022-07-18 /pmc/articles/PMC9308016/ /pubmed/35848903 http://dx.doi.org/10.1167/jov.22.8.11 Text en Copyright 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Article
Lee, Barry B.
Swanson, William H.
Detection and discrimination of achromatic contrast: A ganglion cell perspective
title Detection and discrimination of achromatic contrast: A ganglion cell perspective
title_full Detection and discrimination of achromatic contrast: A ganglion cell perspective
title_fullStr Detection and discrimination of achromatic contrast: A ganglion cell perspective
title_full_unstemmed Detection and discrimination of achromatic contrast: A ganglion cell perspective
title_short Detection and discrimination of achromatic contrast: A ganglion cell perspective
title_sort detection and discrimination of achromatic contrast: a ganglion cell perspective
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308016/
https://www.ncbi.nlm.nih.gov/pubmed/35848903
http://dx.doi.org/10.1167/jov.22.8.11
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