Cargando…

Neural mechanisms to incorporate visual counterevidence in self motion estimation

In selecting appropriate behaviors, animals should weigh sensory evidence both for and against specific beliefs about the world. For instance, animals measure optic flow to estimate and control their own rotation. However, existing models of flow detection can confuse the movement of external object...

Descripción completa

Detalles Bibliográficos
Autores principales: Tanaka, Ryosuke, Zhou, Baohua, Agrochao, Margarida, Badwan, Bara A., Au, Braedyn, Matos, Natalia C. B., Clark, Damon A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881891/
https://www.ncbi.nlm.nih.gov/pubmed/36711843
http://dx.doi.org/10.1101/2023.01.04.522814
_version_ 1784879203137617920
author Tanaka, Ryosuke
Zhou, Baohua
Agrochao, Margarida
Badwan, Bara A.
Au, Braedyn
Matos, Natalia C. B.
Clark, Damon A.
author_facet Tanaka, Ryosuke
Zhou, Baohua
Agrochao, Margarida
Badwan, Bara A.
Au, Braedyn
Matos, Natalia C. B.
Clark, Damon A.
author_sort Tanaka, Ryosuke
collection PubMed
description In selecting appropriate behaviors, animals should weigh sensory evidence both for and against specific beliefs about the world. For instance, animals measure optic flow to estimate and control their own rotation. However, existing models of flow detection can confuse the movement of external objects with genuine self motion. Here, we show that stationary patterns on the retina, which constitute negative evidence against self rotation, are used by the fruit fly Drosophila to suppress inappropriate stabilizing rotational behavior. In silico experiments show that artificial neural networks optimized to distinguish self and world motion similarly detect stationarity and incorporate negative evidence. Employing neural measurements and genetic manipulations, we identified components of the circuitry for stationary pattern detection, which runs parallel to the fly’s motion- and optic flow-detectors. Our results exemplify how the compact brain of the fly incorporates negative evidence to improve heading stability, exploiting geometrical constraints of the visual world.
format Online
Article
Text
id pubmed-9881891
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-98818912023-01-28 Neural mechanisms to incorporate visual counterevidence in self motion estimation Tanaka, Ryosuke Zhou, Baohua Agrochao, Margarida Badwan, Bara A. Au, Braedyn Matos, Natalia C. B. Clark, Damon A. bioRxiv Article In selecting appropriate behaviors, animals should weigh sensory evidence both for and against specific beliefs about the world. For instance, animals measure optic flow to estimate and control their own rotation. However, existing models of flow detection can confuse the movement of external objects with genuine self motion. Here, we show that stationary patterns on the retina, which constitute negative evidence against self rotation, are used by the fruit fly Drosophila to suppress inappropriate stabilizing rotational behavior. In silico experiments show that artificial neural networks optimized to distinguish self and world motion similarly detect stationarity and incorporate negative evidence. Employing neural measurements and genetic manipulations, we identified components of the circuitry for stationary pattern detection, which runs parallel to the fly’s motion- and optic flow-detectors. Our results exemplify how the compact brain of the fly incorporates negative evidence to improve heading stability, exploiting geometrical constraints of the visual world. Cold Spring Harbor Laboratory 2023-07-11 /pmc/articles/PMC9881891/ /pubmed/36711843 http://dx.doi.org/10.1101/2023.01.04.522814 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Tanaka, Ryosuke
Zhou, Baohua
Agrochao, Margarida
Badwan, Bara A.
Au, Braedyn
Matos, Natalia C. B.
Clark, Damon A.
Neural mechanisms to incorporate visual counterevidence in self motion estimation
title Neural mechanisms to incorporate visual counterevidence in self motion estimation
title_full Neural mechanisms to incorporate visual counterevidence in self motion estimation
title_fullStr Neural mechanisms to incorporate visual counterevidence in self motion estimation
title_full_unstemmed Neural mechanisms to incorporate visual counterevidence in self motion estimation
title_short Neural mechanisms to incorporate visual counterevidence in self motion estimation
title_sort neural mechanisms to incorporate visual counterevidence in self motion estimation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881891/
https://www.ncbi.nlm.nih.gov/pubmed/36711843
http://dx.doi.org/10.1101/2023.01.04.522814
work_keys_str_mv AT tanakaryosuke neuralmechanismstoincorporatevisualcounterevidenceinselfmotionestimation
AT zhoubaohua neuralmechanismstoincorporatevisualcounterevidenceinselfmotionestimation
AT agrochaomargarida neuralmechanismstoincorporatevisualcounterevidenceinselfmotionestimation
AT badwanbaraa neuralmechanismstoincorporatevisualcounterevidenceinselfmotionestimation
AT aubraedyn neuralmechanismstoincorporatevisualcounterevidenceinselfmotionestimation
AT matosnataliacb neuralmechanismstoincorporatevisualcounterevidenceinselfmotionestimation
AT clarkdamona neuralmechanismstoincorporatevisualcounterevidenceinselfmotionestimation