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Connecting empirical phenomena and theoretical models of biological coordination across scales
Coordination in living systems—from cells to people—must be understood at multiple levels of description. Analyses and modelling of empirically observed patterns of biological coordination often focus either on ensemble-level statistics in large-scale systems with many components, or on detailed dyn...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731488/ https://www.ncbi.nlm.nih.gov/pubmed/31409241 http://dx.doi.org/10.1098/rsif.2019.0360 |
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author | Zhang, Mengsen Beetle, Christopher Kelso, J. A. Scott Tognoli, Emmanuelle |
author_facet | Zhang, Mengsen Beetle, Christopher Kelso, J. A. Scott Tognoli, Emmanuelle |
author_sort | Zhang, Mengsen |
collection | PubMed |
description | Coordination in living systems—from cells to people—must be understood at multiple levels of description. Analyses and modelling of empirically observed patterns of biological coordination often focus either on ensemble-level statistics in large-scale systems with many components, or on detailed dynamics in small-scale systems with few components. The two approaches have proceeded largely independent of each other. To bridge this gap between levels and scales, we have recently conducted a human experiment of mid-scale social coordination specifically designed to reveal coordination at multiple levels (ensemble, subgroups and dyads) simultaneously. Based on this experiment, the present work shows that, surprisingly, a single system of equations captures key observations at all relevant levels. It also connects empirically validated models of large- and small-scale biological coordination—the Kuramoto and extended Haken–Kelso–Bunz (HKB) models—and the hallmark phenomena that each is known to capture. For example, it exhibits both multistability and metastability observed in small-scale empirical research (via the second-order coupling and symmetry breaking in extended HKB) and the growth of biological complexity as a function of scale (via the scalability of the Kuramoto model). Only by incorporating both of these features simultaneously can we reproduce the essential coordination behaviour observed in our experiment. |
format | Online Article Text |
id | pubmed-6731488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-67314882019-09-09 Connecting empirical phenomena and theoretical models of biological coordination across scales Zhang, Mengsen Beetle, Christopher Kelso, J. A. Scott Tognoli, Emmanuelle J R Soc Interface Life Sciences–Mathematics interface Coordination in living systems—from cells to people—must be understood at multiple levels of description. Analyses and modelling of empirically observed patterns of biological coordination often focus either on ensemble-level statistics in large-scale systems with many components, or on detailed dynamics in small-scale systems with few components. The two approaches have proceeded largely independent of each other. To bridge this gap between levels and scales, we have recently conducted a human experiment of mid-scale social coordination specifically designed to reveal coordination at multiple levels (ensemble, subgroups and dyads) simultaneously. Based on this experiment, the present work shows that, surprisingly, a single system of equations captures key observations at all relevant levels. It also connects empirically validated models of large- and small-scale biological coordination—the Kuramoto and extended Haken–Kelso–Bunz (HKB) models—and the hallmark phenomena that each is known to capture. For example, it exhibits both multistability and metastability observed in small-scale empirical research (via the second-order coupling and symmetry breaking in extended HKB) and the growth of biological complexity as a function of scale (via the scalability of the Kuramoto model). Only by incorporating both of these features simultaneously can we reproduce the essential coordination behaviour observed in our experiment. The Royal Society 2019-08 2019-08-14 /pmc/articles/PMC6731488/ /pubmed/31409241 http://dx.doi.org/10.1098/rsif.2019.0360 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Mathematics interface Zhang, Mengsen Beetle, Christopher Kelso, J. A. Scott Tognoli, Emmanuelle Connecting empirical phenomena and theoretical models of biological coordination across scales |
title | Connecting empirical phenomena and theoretical models of biological coordination across scales |
title_full | Connecting empirical phenomena and theoretical models of biological coordination across scales |
title_fullStr | Connecting empirical phenomena and theoretical models of biological coordination across scales |
title_full_unstemmed | Connecting empirical phenomena and theoretical models of biological coordination across scales |
title_short | Connecting empirical phenomena and theoretical models of biological coordination across scales |
title_sort | connecting empirical phenomena and theoretical models of biological coordination across scales |
topic | Life Sciences–Mathematics interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731488/ https://www.ncbi.nlm.nih.gov/pubmed/31409241 http://dx.doi.org/10.1098/rsif.2019.0360 |
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