Trading speed and accuracy by coding time: a coupled-circuit cortical model.

Our actions take place in space and time, but despite the role of time in decision theory and the growing acknowledgement that the encoding of time is crucial to behaviour, few studies have considered the interactions between neural codes for objects in space and for elapsed time during perceptual d...

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Autores principales: Dominic Standage, Hongzhi You, Da-Hui Wang, Michael C Dorris
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Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/04294ff4ebe149bb88cb279fe5dc9140
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spelling oai:doaj.org-article:04294ff4ebe149bb88cb279fe5dc91402021-11-18T05:52:14ZTrading speed and accuracy by coding time: a coupled-circuit cortical model.1553-734X1553-735810.1371/journal.pcbi.1003021https://doaj.org/article/04294ff4ebe149bb88cb279fe5dc91402013-04-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23592967/pdf/?tool=EBIhttps://doaj.org/toc/1553-734Xhttps://doaj.org/toc/1553-7358Our actions take place in space and time, but despite the role of time in decision theory and the growing acknowledgement that the encoding of time is crucial to behaviour, few studies have considered the interactions between neural codes for objects in space and for elapsed time during perceptual decisions. The speed-accuracy trade-off (SAT) provides a window into spatiotemporal interactions. Our hypothesis is that temporal coding determines the rate at which spatial evidence is integrated, controlling the SAT by gain modulation. Here, we propose that local cortical circuits are inherently suited to the relevant spatial and temporal coding. In simulations of an interval estimation task, we use a generic local-circuit model to encode time by 'climbing' activity, seen in cortex during tasks with a timing requirement. The model is a network of simulated pyramidal cells and inhibitory interneurons, connected by conductance synapses. A simple learning rule enables the network to quickly produce new interval estimates, which show signature characteristics of estimates by experimental subjects. Analysis of network dynamics formally characterizes this generic, local-circuit timing mechanism. In simulations of a perceptual decision task, we couple two such networks. Network function is determined only by spatial selectivity and NMDA receptor conductance strength; all other parameters are identical. To trade speed and accuracy, the timing network simply learns longer or shorter intervals, driving the rate of downstream decision processing by spatially non-selective input, an established form of gain modulation. Like the timing network's interval estimates, decision times show signature characteristics of those by experimental subjects. Overall, we propose, demonstrate and analyse a generic mechanism for timing, a generic mechanism for modulation of decision processing by temporal codes, and we make predictions for experimental verification.Dominic StandageHongzhi YouDa-Hui WangMichael C DorrisPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Computational Biology, Vol 9, Iss 4, p e1003021 (2013)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Dominic Standage
Hongzhi You
Da-Hui Wang
Michael C Dorris
Trading speed and accuracy by coding time: a coupled-circuit cortical model.
description Our actions take place in space and time, but despite the role of time in decision theory and the growing acknowledgement that the encoding of time is crucial to behaviour, few studies have considered the interactions between neural codes for objects in space and for elapsed time during perceptual decisions. The speed-accuracy trade-off (SAT) provides a window into spatiotemporal interactions. Our hypothesis is that temporal coding determines the rate at which spatial evidence is integrated, controlling the SAT by gain modulation. Here, we propose that local cortical circuits are inherently suited to the relevant spatial and temporal coding. In simulations of an interval estimation task, we use a generic local-circuit model to encode time by 'climbing' activity, seen in cortex during tasks with a timing requirement. The model is a network of simulated pyramidal cells and inhibitory interneurons, connected by conductance synapses. A simple learning rule enables the network to quickly produce new interval estimates, which show signature characteristics of estimates by experimental subjects. Analysis of network dynamics formally characterizes this generic, local-circuit timing mechanism. In simulations of a perceptual decision task, we couple two such networks. Network function is determined only by spatial selectivity and NMDA receptor conductance strength; all other parameters are identical. To trade speed and accuracy, the timing network simply learns longer or shorter intervals, driving the rate of downstream decision processing by spatially non-selective input, an established form of gain modulation. Like the timing network's interval estimates, decision times show signature characteristics of those by experimental subjects. Overall, we propose, demonstrate and analyse a generic mechanism for timing, a generic mechanism for modulation of decision processing by temporal codes, and we make predictions for experimental verification.
format article
author Dominic Standage
Hongzhi You
Da-Hui Wang
Michael C Dorris
author_facet Dominic Standage
Hongzhi You
Da-Hui Wang
Michael C Dorris
author_sort Dominic Standage
title Trading speed and accuracy by coding time: a coupled-circuit cortical model.
title_short Trading speed and accuracy by coding time: a coupled-circuit cortical model.
title_full Trading speed and accuracy by coding time: a coupled-circuit cortical model.
title_fullStr Trading speed and accuracy by coding time: a coupled-circuit cortical model.
title_full_unstemmed Trading speed and accuracy by coding time: a coupled-circuit cortical model.
title_sort trading speed and accuracy by coding time: a coupled-circuit cortical model.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/04294ff4ebe149bb88cb279fe5dc9140
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AT hongzhiyou tradingspeedandaccuracybycodingtimeacoupledcircuitcorticalmodel
AT dahuiwang tradingspeedandaccuracybycodingtimeacoupledcircuitcorticalmodel
AT michaelcdorris tradingspeedandaccuracybycodingtimeacoupledcircuitcorticalmodel
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