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Behavioural variation among workers promotes feed-forward loops in a simulated insect colony
Coordinated responses in eusocial insect colonies arise from worker interaction networks that enable collective processing of ecologically relevant information. Previous studies have detected a structural motif in these networks known as the feed-forward loop, which functions to process information...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889185/ https://www.ncbi.nlm.nih.gov/pubmed/35316950 http://dx.doi.org/10.1098/rsos.220120 |
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author | Easter, Carrie Leadbeater, Ellouise Hasenjager, Matthew J. |
author_facet | Easter, Carrie Leadbeater, Ellouise Hasenjager, Matthew J. |
author_sort | Easter, Carrie |
collection | PubMed |
description | Coordinated responses in eusocial insect colonies arise from worker interaction networks that enable collective processing of ecologically relevant information. Previous studies have detected a structural motif in these networks known as the feed-forward loop, which functions to process information in other biological regulatory networks (e.g. transcriptional networks). However, the processes that generate feed-forward loops among workers and the consequences for information flow within the colony remain largely unexplored. We constructed an agent-based model to investigate how individual variation in activity and movement shaped the production of feed-forward loops in a simulated insect colony. We hypothesized that individual variation along these axes would generate feed-forward loops by driving variation in interaction frequency among workers. We found that among-individual variation in activity drove over-representation of feed-forward loops in the interaction networks by determining the directionality of interactions. However, despite previous work linking feed-forward loops with efficient information transfer, activity variation did not promote faster or more efficient information flow, thus providing no support for the hypothesis that feed-forward loops reflect selection for enhanced collective functioning. Conversely, individual variation in movement trajectory, despite playing no role in generating feed-forward loops, promoted fast and efficient information flow by linking together otherwise unconnected regions of the nest. |
format | Online Article Text |
id | pubmed-8889185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88891852022-03-21 Behavioural variation among workers promotes feed-forward loops in a simulated insect colony Easter, Carrie Leadbeater, Ellouise Hasenjager, Matthew J. R Soc Open Sci Ecology, Conservation and Global Change Biology Coordinated responses in eusocial insect colonies arise from worker interaction networks that enable collective processing of ecologically relevant information. Previous studies have detected a structural motif in these networks known as the feed-forward loop, which functions to process information in other biological regulatory networks (e.g. transcriptional networks). However, the processes that generate feed-forward loops among workers and the consequences for information flow within the colony remain largely unexplored. We constructed an agent-based model to investigate how individual variation in activity and movement shaped the production of feed-forward loops in a simulated insect colony. We hypothesized that individual variation along these axes would generate feed-forward loops by driving variation in interaction frequency among workers. We found that among-individual variation in activity drove over-representation of feed-forward loops in the interaction networks by determining the directionality of interactions. However, despite previous work linking feed-forward loops with efficient information transfer, activity variation did not promote faster or more efficient information flow, thus providing no support for the hypothesis that feed-forward loops reflect selection for enhanced collective functioning. Conversely, individual variation in movement trajectory, despite playing no role in generating feed-forward loops, promoted fast and efficient information flow by linking together otherwise unconnected regions of the nest. The Royal Society 2022-03-02 /pmc/articles/PMC8889185/ /pubmed/35316950 http://dx.doi.org/10.1098/rsos.220120 Text en © 2022 The Authors. https://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/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Ecology, Conservation and Global Change Biology Easter, Carrie Leadbeater, Ellouise Hasenjager, Matthew J. Behavioural variation among workers promotes feed-forward loops in a simulated insect colony |
title | Behavioural variation among workers promotes feed-forward loops in a simulated insect colony |
title_full | Behavioural variation among workers promotes feed-forward loops in a simulated insect colony |
title_fullStr | Behavioural variation among workers promotes feed-forward loops in a simulated insect colony |
title_full_unstemmed | Behavioural variation among workers promotes feed-forward loops in a simulated insect colony |
title_short | Behavioural variation among workers promotes feed-forward loops in a simulated insect colony |
title_sort | behavioural variation among workers promotes feed-forward loops in a simulated insect colony |
topic | Ecology, Conservation and Global Change Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889185/ https://www.ncbi.nlm.nih.gov/pubmed/35316950 http://dx.doi.org/10.1098/rsos.220120 |
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