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On the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold Physarum polycephalum
The plasmodium of slime mold Physarum polycephalum behaves as an amorphous reaction-diffusion computing substrate and is capable of apparently ‘intelligent’ behavior. But how does intelligence emerge in an acellular organism? Through a range of laboratory experiments, we visualize the plasmodial cyt...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594612/ https://www.ncbi.nlm.nih.gov/pubmed/26478782 http://dx.doi.org/10.1080/19420889.2015.1059007 |
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author | Mayne, Richard Adamatzky, Andrew Jones, Jeff |
author_facet | Mayne, Richard Adamatzky, Andrew Jones, Jeff |
author_sort | Mayne, Richard |
collection | PubMed |
description | The plasmodium of slime mold Physarum polycephalum behaves as an amorphous reaction-diffusion computing substrate and is capable of apparently ‘intelligent’ behavior. But how does intelligence emerge in an acellular organism? Through a range of laboratory experiments, we visualize the plasmodial cytoskeleton—a ubiquitous cellular protein scaffold whose functions are manifold and essential to life—and discuss its putative role as a network for transducing, transmitting and structuring data streams within the plasmodium. Through a range of computer modeling techniques, we demonstrate how emergent behavior, and hence computational intelligence, may occur in cytoskeletal communications networks. Specifically, we model the topology of both the actin and tubulin cytoskeletal networks and discuss how computation may occur therein. Furthermore, we present bespoke cellular automata and particle swarm models for the computational process within the cytoskeleton and observe the incidence of emergent patterns in both. Our work grants unique insight into the origins of natural intelligence; the results presented here are therefore readily transferable to the fields of natural computation, cell biology and biomedical science. We conclude by discussing how our results may alter our biological, computational and philosophical understanding of intelligence and consciousness. |
format | Online Article Text |
id | pubmed-4594612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-45946122015-10-16 On the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold Physarum polycephalum Mayne, Richard Adamatzky, Andrew Jones, Jeff Commun Integr Biol Research Paper The plasmodium of slime mold Physarum polycephalum behaves as an amorphous reaction-diffusion computing substrate and is capable of apparently ‘intelligent’ behavior. But how does intelligence emerge in an acellular organism? Through a range of laboratory experiments, we visualize the plasmodial cytoskeleton—a ubiquitous cellular protein scaffold whose functions are manifold and essential to life—and discuss its putative role as a network for transducing, transmitting and structuring data streams within the plasmodium. Through a range of computer modeling techniques, we demonstrate how emergent behavior, and hence computational intelligence, may occur in cytoskeletal communications networks. Specifically, we model the topology of both the actin and tubulin cytoskeletal networks and discuss how computation may occur therein. Furthermore, we present bespoke cellular automata and particle swarm models for the computational process within the cytoskeleton and observe the incidence of emergent patterns in both. Our work grants unique insight into the origins of natural intelligence; the results presented here are therefore readily transferable to the fields of natural computation, cell biology and biomedical science. We conclude by discussing how our results may alter our biological, computational and philosophical understanding of intelligence and consciousness. Taylor & Francis 2015-08-31 /pmc/articles/PMC4594612/ /pubmed/26478782 http://dx.doi.org/10.1080/19420889.2015.1059007 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Research Paper Mayne, Richard Adamatzky, Andrew Jones, Jeff On the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold Physarum polycephalum |
title | On the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold Physarum polycephalum |
title_full | On the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold Physarum polycephalum |
title_fullStr | On the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold Physarum polycephalum |
title_full_unstemmed | On the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold Physarum polycephalum |
title_short | On the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold Physarum polycephalum |
title_sort | on the role of the plasmodial cytoskeleton in facilitating intelligent behavior in slime mold physarum polycephalum |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594612/ https://www.ncbi.nlm.nih.gov/pubmed/26478782 http://dx.doi.org/10.1080/19420889.2015.1059007 |
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