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Error-Based Analysis of Optimal Tuning Functions Explains Phenomena Observed in Sensory Neurons
Biological systems display impressive capabilities in effectively responding to environmental signals in real time. There is increasing evidence that organisms may indeed be employing near optimal Bayesian calculations in their decision-making. An intriguing question relates to the properties of opt...
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Formato: | Texto |
Lenguaje: | English |
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Frontiers Research Foundation
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978036/ https://www.ncbi.nlm.nih.gov/pubmed/21079749 http://dx.doi.org/10.3389/fncom.2010.00130 |
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author | Yaeli, Steve Meir, Ron |
author_facet | Yaeli, Steve Meir, Ron |
author_sort | Yaeli, Steve |
collection | PubMed |
description | Biological systems display impressive capabilities in effectively responding to environmental signals in real time. There is increasing evidence that organisms may indeed be employing near optimal Bayesian calculations in their decision-making. An intriguing question relates to the properties of optimal encoding methods, namely determining the properties of neural populations in sensory layers that optimize performance, subject to physiological constraints. Within an ecological theory of neural encoding/decoding, we show that optimal Bayesian performance requires neural adaptation which reflects environmental changes. Specifically, we predict that neuronal tuning functions possess an optimal width, which increases with prior uncertainty and environmental noise, and decreases with the decoding time window. Furthermore, even for static stimuli, we demonstrate that dynamic sensory tuning functions, acting at relatively short time scales, lead to improved performance. Interestingly, the narrowing of tuning functions as a function of time was recently observed in several biological systems. Such results set the stage for a functional theory which may explain the high reliability of sensory systems, and the utility of neuronal adaptation occurring at multiple time scales. |
format | Text |
id | pubmed-2978036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-29780362010-11-15 Error-Based Analysis of Optimal Tuning Functions Explains Phenomena Observed in Sensory Neurons Yaeli, Steve Meir, Ron Front Comput Neurosci Neuroscience Biological systems display impressive capabilities in effectively responding to environmental signals in real time. There is increasing evidence that organisms may indeed be employing near optimal Bayesian calculations in their decision-making. An intriguing question relates to the properties of optimal encoding methods, namely determining the properties of neural populations in sensory layers that optimize performance, subject to physiological constraints. Within an ecological theory of neural encoding/decoding, we show that optimal Bayesian performance requires neural adaptation which reflects environmental changes. Specifically, we predict that neuronal tuning functions possess an optimal width, which increases with prior uncertainty and environmental noise, and decreases with the decoding time window. Furthermore, even for static stimuli, we demonstrate that dynamic sensory tuning functions, acting at relatively short time scales, lead to improved performance. Interestingly, the narrowing of tuning functions as a function of time was recently observed in several biological systems. Such results set the stage for a functional theory which may explain the high reliability of sensory systems, and the utility of neuronal adaptation occurring at multiple time scales. Frontiers Research Foundation 2010-10-14 /pmc/articles/PMC2978036/ /pubmed/21079749 http://dx.doi.org/10.3389/fncom.2010.00130 Text en Copyright © 2010 Yaeli and Meir. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited. |
spellingShingle | Neuroscience Yaeli, Steve Meir, Ron Error-Based Analysis of Optimal Tuning Functions Explains Phenomena Observed in Sensory Neurons |
title | Error-Based Analysis of Optimal Tuning Functions Explains Phenomena Observed in Sensory Neurons |
title_full | Error-Based Analysis of Optimal Tuning Functions Explains Phenomena Observed in Sensory Neurons |
title_fullStr | Error-Based Analysis of Optimal Tuning Functions Explains Phenomena Observed in Sensory Neurons |
title_full_unstemmed | Error-Based Analysis of Optimal Tuning Functions Explains Phenomena Observed in Sensory Neurons |
title_short | Error-Based Analysis of Optimal Tuning Functions Explains Phenomena Observed in Sensory Neurons |
title_sort | error-based analysis of optimal tuning functions explains phenomena observed in sensory neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978036/ https://www.ncbi.nlm.nih.gov/pubmed/21079749 http://dx.doi.org/10.3389/fncom.2010.00130 |
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