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Short-term activity cycles impede information transmission in ant colonies

Rhythmical activity patterns are ubiquitous in nature. We study an oscillatory biological system: collective activity cycles in ant colonies. Ant colonies have become model systems for research on biological networks because the interactions between the component parts are visible to the naked eye,...

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Detalles Bibliográficos
Autores principales: Richardson, Thomas O., Liechti, Jonas I., Stroeymeyt, Nathalie, Bonhoeffer, Sebastian, Keller, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443549/
https://www.ncbi.nlm.nih.gov/pubmed/28489896
http://dx.doi.org/10.1371/journal.pcbi.1005527
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author Richardson, Thomas O.
Liechti, Jonas I.
Stroeymeyt, Nathalie
Bonhoeffer, Sebastian
Keller, Laurent
author_facet Richardson, Thomas O.
Liechti, Jonas I.
Stroeymeyt, Nathalie
Bonhoeffer, Sebastian
Keller, Laurent
author_sort Richardson, Thomas O.
collection PubMed
description Rhythmical activity patterns are ubiquitous in nature. We study an oscillatory biological system: collective activity cycles in ant colonies. Ant colonies have become model systems for research on biological networks because the interactions between the component parts are visible to the naked eye, and because the time-ordered contact network formed by these interactions serves as the substrate for the distribution of information and other resources throughout the colony. To understand how the collective activity cycles influence the contact network transport properties, we used an automated tracking system to record the movement of all the individuals within nine different ant colonies. From these trajectories we extracted over two million ant-to-ant interactions. Time-series analysis of the temporal fluctuations of the overall colony interaction and movement rates revealed that both the period and amplitude of the activity cycles exhibit a diurnal cycle, in which daytime cycles are faster and of greater amplitude than night cycles. Using epidemiology-derived models of transmission over networks, we compared the transmission properties of the observed periodic contact networks with those of synthetic aperiodic networks. These simulations revealed that contrary to some predictions, regularly-oscillating contact networks should impede information transmission. Further, we provide a mechanistic explanation for this effect, and present evidence in support of it.
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spelling pubmed-54435492017-06-06 Short-term activity cycles impede information transmission in ant colonies Richardson, Thomas O. Liechti, Jonas I. Stroeymeyt, Nathalie Bonhoeffer, Sebastian Keller, Laurent PLoS Comput Biol Research Article Rhythmical activity patterns are ubiquitous in nature. We study an oscillatory biological system: collective activity cycles in ant colonies. Ant colonies have become model systems for research on biological networks because the interactions between the component parts are visible to the naked eye, and because the time-ordered contact network formed by these interactions serves as the substrate for the distribution of information and other resources throughout the colony. To understand how the collective activity cycles influence the contact network transport properties, we used an automated tracking system to record the movement of all the individuals within nine different ant colonies. From these trajectories we extracted over two million ant-to-ant interactions. Time-series analysis of the temporal fluctuations of the overall colony interaction and movement rates revealed that both the period and amplitude of the activity cycles exhibit a diurnal cycle, in which daytime cycles are faster and of greater amplitude than night cycles. Using epidemiology-derived models of transmission over networks, we compared the transmission properties of the observed periodic contact networks with those of synthetic aperiodic networks. These simulations revealed that contrary to some predictions, regularly-oscillating contact networks should impede information transmission. Further, we provide a mechanistic explanation for this effect, and present evidence in support of it. Public Library of Science 2017-05-10 /pmc/articles/PMC5443549/ /pubmed/28489896 http://dx.doi.org/10.1371/journal.pcbi.1005527 Text en © 2017 Richardson et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Richardson, Thomas O.
Liechti, Jonas I.
Stroeymeyt, Nathalie
Bonhoeffer, Sebastian
Keller, Laurent
Short-term activity cycles impede information transmission in ant colonies
title Short-term activity cycles impede information transmission in ant colonies
title_full Short-term activity cycles impede information transmission in ant colonies
title_fullStr Short-term activity cycles impede information transmission in ant colonies
title_full_unstemmed Short-term activity cycles impede information transmission in ant colonies
title_short Short-term activity cycles impede information transmission in ant colonies
title_sort short-term activity cycles impede information transmission in ant colonies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5443549/
https://www.ncbi.nlm.nih.gov/pubmed/28489896
http://dx.doi.org/10.1371/journal.pcbi.1005527
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