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Training Transfers the Limits on Perception from Parietal to Ventral Cortex

Visually guided behavior depends on (1) extracting and (2) discriminating signals from complex retinal inputs, and these perceptual skills improve with practice [1]. For instance, training on aerial reconnaissance facilitated World War II Allied military operations [2]; analysts pored over stereosco...

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Autores principales: Chang, Dorita H.F., Mevorach, Carmel, Kourtzi, Zoe, Welchman, Andrew E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204932/
https://www.ncbi.nlm.nih.gov/pubmed/25283780
http://dx.doi.org/10.1016/j.cub.2014.08.058
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author Chang, Dorita H.F.
Mevorach, Carmel
Kourtzi, Zoe
Welchman, Andrew E.
author_facet Chang, Dorita H.F.
Mevorach, Carmel
Kourtzi, Zoe
Welchman, Andrew E.
author_sort Chang, Dorita H.F.
collection PubMed
description Visually guided behavior depends on (1) extracting and (2) discriminating signals from complex retinal inputs, and these perceptual skills improve with practice [1]. For instance, training on aerial reconnaissance facilitated World War II Allied military operations [2]; analysts pored over stereoscopic photographs, becoming expert at (1) segmenting pictures into meaningful items to break camouflage from (noisy) backgrounds, and (2) discriminating fine details to distinguish V-weapons from innocuous pylons. Training is understood to optimize neural circuits that process scene features (e.g., orientation) for particular purposes (e.g., judging position) [3, 4, 5, 6]. Yet learning is most beneficial when it generalizes to other settings [7, 8] and is critical in recovery after adversity [9], challenging understanding of the circuitry involved. Here we used repetitive transcranial magnetic stimulation (rTMS) to infer the functional organization supporting learning generalization in the human brain. First, we show dissociable contributions of the posterior parietal cortex (PPC) versus lateral occipital (LO) circuits: extracting targets from noise is disrupted by PPC stimulation, in contrast to judging feature differences, which is affected by LO rTMS. Then, we demonstrate that training causes striking changes in this circuit: after feature training, identifying a target in noise is not disrupted by PPC stimulation but instead by LO stimulation. This indicates that training shifts the limits on perception from parietal to ventral brain regions and identifies a critical neural circuit for visual learning. We suggest that generalization is implemented by supplanting dynamic processing conducted in the PPC with specific feature templates stored in the ventral cortex.
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spelling pubmed-42049322014-10-27 Training Transfers the Limits on Perception from Parietal to Ventral Cortex Chang, Dorita H.F. Mevorach, Carmel Kourtzi, Zoe Welchman, Andrew E. Curr Biol Report Visually guided behavior depends on (1) extracting and (2) discriminating signals from complex retinal inputs, and these perceptual skills improve with practice [1]. For instance, training on aerial reconnaissance facilitated World War II Allied military operations [2]; analysts pored over stereoscopic photographs, becoming expert at (1) segmenting pictures into meaningful items to break camouflage from (noisy) backgrounds, and (2) discriminating fine details to distinguish V-weapons from innocuous pylons. Training is understood to optimize neural circuits that process scene features (e.g., orientation) for particular purposes (e.g., judging position) [3, 4, 5, 6]. Yet learning is most beneficial when it generalizes to other settings [7, 8] and is critical in recovery after adversity [9], challenging understanding of the circuitry involved. Here we used repetitive transcranial magnetic stimulation (rTMS) to infer the functional organization supporting learning generalization in the human brain. First, we show dissociable contributions of the posterior parietal cortex (PPC) versus lateral occipital (LO) circuits: extracting targets from noise is disrupted by PPC stimulation, in contrast to judging feature differences, which is affected by LO rTMS. Then, we demonstrate that training causes striking changes in this circuit: after feature training, identifying a target in noise is not disrupted by PPC stimulation but instead by LO stimulation. This indicates that training shifts the limits on perception from parietal to ventral brain regions and identifies a critical neural circuit for visual learning. We suggest that generalization is implemented by supplanting dynamic processing conducted in the PPC with specific feature templates stored in the ventral cortex. Cell Press 2014-10-20 /pmc/articles/PMC4204932/ /pubmed/25283780 http://dx.doi.org/10.1016/j.cub.2014.08.058 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Report
Chang, Dorita H.F.
Mevorach, Carmel
Kourtzi, Zoe
Welchman, Andrew E.
Training Transfers the Limits on Perception from Parietal to Ventral Cortex
title Training Transfers the Limits on Perception from Parietal to Ventral Cortex
title_full Training Transfers the Limits on Perception from Parietal to Ventral Cortex
title_fullStr Training Transfers the Limits on Perception from Parietal to Ventral Cortex
title_full_unstemmed Training Transfers the Limits on Perception from Parietal to Ventral Cortex
title_short Training Transfers the Limits on Perception from Parietal to Ventral Cortex
title_sort training transfers the limits on perception from parietal to ventral cortex
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204932/
https://www.ncbi.nlm.nih.gov/pubmed/25283780
http://dx.doi.org/10.1016/j.cub.2014.08.058
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