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Resilience of honeybee colonies via common stomach: A model of self-regulation of foraging

We propose a new regulation mechanism based on the idea of the “common stomach” to explain several aspects of the resilience and homeostatic regulation of honeybee colonies. This mechanism exploits shared pools of substances (pollen, nectar, workers, brood) that modulate recruitment, abandonment and...

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Detalles Bibliográficos
Autores principales: Schmickl, Thomas, Karsai, Istvan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697885/
https://www.ncbi.nlm.nih.gov/pubmed/29161278
http://dx.doi.org/10.1371/journal.pone.0188004
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author Schmickl, Thomas
Karsai, Istvan
author_facet Schmickl, Thomas
Karsai, Istvan
author_sort Schmickl, Thomas
collection PubMed
description We propose a new regulation mechanism based on the idea of the “common stomach” to explain several aspects of the resilience and homeostatic regulation of honeybee colonies. This mechanism exploits shared pools of substances (pollen, nectar, workers, brood) that modulate recruitment, abandonment and allocation patterns at the colony-level and enable bees to perform several survival strategies to cope with difficult circumstances: Lack of proteins leads to reduced feeding of young brood, to early capping of old brood and to regaining of already spent proteins through brood cannibalism. We modeled this system by linear interaction terms and mass-action law. To test the predictive power of the model of this regulatory mechanism we compared our model predictions to experimental data of several studies. These comparisons show that the proposed regulation mechanism can explain a variety of colony level behaviors. Detailed analysis of the model revealed that these mechanisms could explain the resilience, stability and self-regulation observed in honeybee colonies. We found that manipulation of material flow and applying sudden perturbations to colony stocks are quickly compensated by a resulting counter-acting shift in task selection. Selective analysis of feedback loops allowed us to discriminate the importance of different feedback loops in self-regulation of honeybee colonies. We stress that a network of simple proximate mechanisms can explain significant colony-level abilities that can also be seen as ultimate reasoning of the evolutionary trajectory of honeybees.
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spelling pubmed-56978852017-11-30 Resilience of honeybee colonies via common stomach: A model of self-regulation of foraging Schmickl, Thomas Karsai, Istvan PLoS One Research Article We propose a new regulation mechanism based on the idea of the “common stomach” to explain several aspects of the resilience and homeostatic regulation of honeybee colonies. This mechanism exploits shared pools of substances (pollen, nectar, workers, brood) that modulate recruitment, abandonment and allocation patterns at the colony-level and enable bees to perform several survival strategies to cope with difficult circumstances: Lack of proteins leads to reduced feeding of young brood, to early capping of old brood and to regaining of already spent proteins through brood cannibalism. We modeled this system by linear interaction terms and mass-action law. To test the predictive power of the model of this regulatory mechanism we compared our model predictions to experimental data of several studies. These comparisons show that the proposed regulation mechanism can explain a variety of colony level behaviors. Detailed analysis of the model revealed that these mechanisms could explain the resilience, stability and self-regulation observed in honeybee colonies. We found that manipulation of material flow and applying sudden perturbations to colony stocks are quickly compensated by a resulting counter-acting shift in task selection. Selective analysis of feedback loops allowed us to discriminate the importance of different feedback loops in self-regulation of honeybee colonies. We stress that a network of simple proximate mechanisms can explain significant colony-level abilities that can also be seen as ultimate reasoning of the evolutionary trajectory of honeybees. Public Library of Science 2017-11-21 /pmc/articles/PMC5697885/ /pubmed/29161278 http://dx.doi.org/10.1371/journal.pone.0188004 Text en © 2017 Schmickl, Karsai 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
Schmickl, Thomas
Karsai, Istvan
Resilience of honeybee colonies via common stomach: A model of self-regulation of foraging
title Resilience of honeybee colonies via common stomach: A model of self-regulation of foraging
title_full Resilience of honeybee colonies via common stomach: A model of self-regulation of foraging
title_fullStr Resilience of honeybee colonies via common stomach: A model of self-regulation of foraging
title_full_unstemmed Resilience of honeybee colonies via common stomach: A model of self-regulation of foraging
title_short Resilience of honeybee colonies via common stomach: A model of self-regulation of foraging
title_sort resilience of honeybee colonies via common stomach: a model of self-regulation of foraging
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697885/
https://www.ncbi.nlm.nih.gov/pubmed/29161278
http://dx.doi.org/10.1371/journal.pone.0188004
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