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Brain Performance versus Phase Transitions

We here illustrate how a well-founded study of the brain may originate in assuming analogies with phase-transition phenomena. Analyzing to what extent a weak signal endures in noisy environments, we identify the underlying mechanisms, and it results a description of how the excitability associated t...

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Detalles Bibliográficos
Autores principales: Torres, Joaquín J., Marro, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507401/
https://www.ncbi.nlm.nih.gov/pubmed/26193453
http://dx.doi.org/10.1038/srep12216
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author Torres, Joaquín J.
Marro, J.
author_facet Torres, Joaquín J.
Marro, J.
author_sort Torres, Joaquín J.
collection PubMed
description We here illustrate how a well-founded study of the brain may originate in assuming analogies with phase-transition phenomena. Analyzing to what extent a weak signal endures in noisy environments, we identify the underlying mechanisms, and it results a description of how the excitability associated to (non-equilibrium) phase changes and criticality optimizes the processing of the signal. Our setting is a network of integrate-and-fire nodes in which connections are heterogeneous with rapid time-varying intensities mimicking fatigue and potentiation. Emergence then becomes quite robust against wiring topology modification—in fact, we considered from a fully connected network to the Homo sapiens connectome—showing the essential role of synaptic flickering on computations. We also suggest how to experimentally disclose significant changes during actual brain operation.
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spelling pubmed-45074012015-07-21 Brain Performance versus Phase Transitions Torres, Joaquín J. Marro, J. Sci Rep Article We here illustrate how a well-founded study of the brain may originate in assuming analogies with phase-transition phenomena. Analyzing to what extent a weak signal endures in noisy environments, we identify the underlying mechanisms, and it results a description of how the excitability associated to (non-equilibrium) phase changes and criticality optimizes the processing of the signal. Our setting is a network of integrate-and-fire nodes in which connections are heterogeneous with rapid time-varying intensities mimicking fatigue and potentiation. Emergence then becomes quite robust against wiring topology modification—in fact, we considered from a fully connected network to the Homo sapiens connectome—showing the essential role of synaptic flickering on computations. We also suggest how to experimentally disclose significant changes during actual brain operation. Nature Publishing Group 2015-07-20 /pmc/articles/PMC4507401/ /pubmed/26193453 http://dx.doi.org/10.1038/srep12216 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Torres, Joaquín J.
Marro, J.
Brain Performance versus Phase Transitions
title Brain Performance versus Phase Transitions
title_full Brain Performance versus Phase Transitions
title_fullStr Brain Performance versus Phase Transitions
title_full_unstemmed Brain Performance versus Phase Transitions
title_short Brain Performance versus Phase Transitions
title_sort brain performance versus phase transitions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507401/
https://www.ncbi.nlm.nih.gov/pubmed/26193453
http://dx.doi.org/10.1038/srep12216
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