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A computational model of the integration of landmarks and motion in the insect central complex

The insect central complex (CX) is an enigmatic structure whose computational function has evaded inquiry, but has been implicated in a wide range of behaviours. Recent experimental evidence from the fruit fly (Drosophila melanogaster) and the cockroach (Blaberus discoidalis) has demonstrated the ex...

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Autores principales: Cope, Alex J., Sabo, Chelsea, Vasilaki, Eleni, Barron, Andrew B., Marshall, James A. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328262/
https://www.ncbi.nlm.nih.gov/pubmed/28241061
http://dx.doi.org/10.1371/journal.pone.0172325
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author Cope, Alex J.
Sabo, Chelsea
Vasilaki, Eleni
Barron, Andrew B.
Marshall, James A. R.
author_facet Cope, Alex J.
Sabo, Chelsea
Vasilaki, Eleni
Barron, Andrew B.
Marshall, James A. R.
author_sort Cope, Alex J.
collection PubMed
description The insect central complex (CX) is an enigmatic structure whose computational function has evaded inquiry, but has been implicated in a wide range of behaviours. Recent experimental evidence from the fruit fly (Drosophila melanogaster) and the cockroach (Blaberus discoidalis) has demonstrated the existence of neural activity corresponding to the animal’s orientation within a virtual arena (a neural ‘compass’), and this provides an insight into one component of the CX structure. There are two key features of the compass activity: an offset between the angle represented by the compass and the true angular position of visual features in the arena, and the remapping of the 270° visual arena onto an entire circle of neurons in the compass. Here we present a computational model which can reproduce this experimental evidence in detail, and predicts the computational mechanisms that underlie the data. We predict that both the offset and remapping of the fly’s orientation onto the neural compass can be explained by plasticity in the synaptic weights between segments of the visual field and the neurons representing orientation. Furthermore, we predict that this learning is reliant on the existence of neural pathways that detect rotational motion across the whole visual field and uses this rotation signal to drive the rotation of activity in a neural ring attractor. Our model also reproduces the ‘transitioning’ between visual landmarks seen when rotationally symmetric landmarks are presented. This model can provide the basis for further investigation into the role of the central complex, which promises to be a key structure for understanding insect behaviour, as well as suggesting approaches towards creating fully autonomous robotic agents.
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spelling pubmed-53282622017-03-09 A computational model of the integration of landmarks and motion in the insect central complex Cope, Alex J. Sabo, Chelsea Vasilaki, Eleni Barron, Andrew B. Marshall, James A. R. PLoS One Research Article The insect central complex (CX) is an enigmatic structure whose computational function has evaded inquiry, but has been implicated in a wide range of behaviours. Recent experimental evidence from the fruit fly (Drosophila melanogaster) and the cockroach (Blaberus discoidalis) has demonstrated the existence of neural activity corresponding to the animal’s orientation within a virtual arena (a neural ‘compass’), and this provides an insight into one component of the CX structure. There are two key features of the compass activity: an offset between the angle represented by the compass and the true angular position of visual features in the arena, and the remapping of the 270° visual arena onto an entire circle of neurons in the compass. Here we present a computational model which can reproduce this experimental evidence in detail, and predicts the computational mechanisms that underlie the data. We predict that both the offset and remapping of the fly’s orientation onto the neural compass can be explained by plasticity in the synaptic weights between segments of the visual field and the neurons representing orientation. Furthermore, we predict that this learning is reliant on the existence of neural pathways that detect rotational motion across the whole visual field and uses this rotation signal to drive the rotation of activity in a neural ring attractor. Our model also reproduces the ‘transitioning’ between visual landmarks seen when rotationally symmetric landmarks are presented. This model can provide the basis for further investigation into the role of the central complex, which promises to be a key structure for understanding insect behaviour, as well as suggesting approaches towards creating fully autonomous robotic agents. Public Library of Science 2017-02-27 /pmc/articles/PMC5328262/ /pubmed/28241061 http://dx.doi.org/10.1371/journal.pone.0172325 Text en © 2017 Cope 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
Cope, Alex J.
Sabo, Chelsea
Vasilaki, Eleni
Barron, Andrew B.
Marshall, James A. R.
A computational model of the integration of landmarks and motion in the insect central complex
title A computational model of the integration of landmarks and motion in the insect central complex
title_full A computational model of the integration of landmarks and motion in the insect central complex
title_fullStr A computational model of the integration of landmarks and motion in the insect central complex
title_full_unstemmed A computational model of the integration of landmarks and motion in the insect central complex
title_short A computational model of the integration of landmarks and motion in the insect central complex
title_sort computational model of the integration of landmarks and motion in the insect central complex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5328262/
https://www.ncbi.nlm.nih.gov/pubmed/28241061
http://dx.doi.org/10.1371/journal.pone.0172325
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