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Nonlinear circuits for naturalistic visual motion estimation
Many animals use visual signals to estimate motion. Canonical models suppose that animals estimate motion by cross-correlating pairs of spatiotemporally separated visual signals, but recent experiments indicate that humans and flies perceive motion from higher-order correlations that signify motion...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663970/ https://www.ncbi.nlm.nih.gov/pubmed/26499494 http://dx.doi.org/10.7554/eLife.09123 |
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author | Fitzgerald, James E Clark, Damon A |
author_facet | Fitzgerald, James E Clark, Damon A |
author_sort | Fitzgerald, James E |
collection | PubMed |
description | Many animals use visual signals to estimate motion. Canonical models suppose that animals estimate motion by cross-correlating pairs of spatiotemporally separated visual signals, but recent experiments indicate that humans and flies perceive motion from higher-order correlations that signify motion in natural environments. Here we show how biologically plausible processing motifs in neural circuits could be tuned to extract this information. We emphasize how known aspects of Drosophila's visual circuitry could embody this tuning and predict fly behavior. We find that segregating motion signals into ON/OFF channels can enhance estimation accuracy by accounting for natural light/dark asymmetries. Furthermore, a diversity of inputs to motion detecting neurons can provide access to more complex higher-order correlations. Collectively, these results illustrate how non-canonical computations improve motion estimation with naturalistic inputs. This argues that the complexity of the fly's motion computations, implemented in its elaborate circuits, represents a valuable feature of its visual motion estimator. DOI: http://dx.doi.org/10.7554/eLife.09123.001 |
format | Online Article Text |
id | pubmed-4663970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46639702015-12-01 Nonlinear circuits for naturalistic visual motion estimation Fitzgerald, James E Clark, Damon A eLife Neuroscience Many animals use visual signals to estimate motion. Canonical models suppose that animals estimate motion by cross-correlating pairs of spatiotemporally separated visual signals, but recent experiments indicate that humans and flies perceive motion from higher-order correlations that signify motion in natural environments. Here we show how biologically plausible processing motifs in neural circuits could be tuned to extract this information. We emphasize how known aspects of Drosophila's visual circuitry could embody this tuning and predict fly behavior. We find that segregating motion signals into ON/OFF channels can enhance estimation accuracy by accounting for natural light/dark asymmetries. Furthermore, a diversity of inputs to motion detecting neurons can provide access to more complex higher-order correlations. Collectively, these results illustrate how non-canonical computations improve motion estimation with naturalistic inputs. This argues that the complexity of the fly's motion computations, implemented in its elaborate circuits, represents a valuable feature of its visual motion estimator. DOI: http://dx.doi.org/10.7554/eLife.09123.001 eLife Sciences Publications, Ltd 2015-10-24 /pmc/articles/PMC4663970/ /pubmed/26499494 http://dx.doi.org/10.7554/eLife.09123 Text en © 2015, Fitzgerald and Clark http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Fitzgerald, James E Clark, Damon A Nonlinear circuits for naturalistic visual motion estimation |
title | Nonlinear circuits for naturalistic visual motion estimation |
title_full | Nonlinear circuits for naturalistic visual motion estimation |
title_fullStr | Nonlinear circuits for naturalistic visual motion estimation |
title_full_unstemmed | Nonlinear circuits for naturalistic visual motion estimation |
title_short | Nonlinear circuits for naturalistic visual motion estimation |
title_sort | nonlinear circuits for naturalistic visual motion estimation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663970/ https://www.ncbi.nlm.nih.gov/pubmed/26499494 http://dx.doi.org/10.7554/eLife.09123 |
work_keys_str_mv | AT fitzgeraldjamese nonlinearcircuitsfornaturalisticvisualmotionestimation AT clarkdamona nonlinearcircuitsfornaturalisticvisualmotionestimation |