Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1782510872278597632 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5328262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT copealexj acomputationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT sabochelsea acomputationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT vasilakieleni acomputationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT barronandrewb acomputationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT marshalljamesar acomputationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT copealexj computationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT sabochelsea computationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT vasilakieleni computationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT barronandrewb computationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex AT marshalljamesar computationalmodeloftheintegrationoflandmarksandmotionintheinsectcentralcomplex |