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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...

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Detalles Bibliográficos
Autores principales: Fitzgerald, James E, Clark, Damon A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
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
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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
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