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Preattentive facilitation of target trajectories in a dragonfly visual neuron

The ability to pursue targets in visually cluttered and distraction-rich environments is critical for predators such as dragonflies. Previously, we identified Centrifugal Small-Target Motion Detector 1 (CSTMD1), a dragonfly visual neuron likely involved in such target-tracking behaviour. CSTMD1 exhi...

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Autores principales: Lancer, Benjamin H., Evans, Bernard J. E., Fabian, Joseph M., O’Carroll, David C., Wiederman, Steven D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388622/
https://www.ncbi.nlm.nih.gov/pubmed/35982305
http://dx.doi.org/10.1038/s42003-022-03798-8
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author Lancer, Benjamin H.
Evans, Bernard J. E.
Fabian, Joseph M.
O’Carroll, David C.
Wiederman, Steven D.
author_facet Lancer, Benjamin H.
Evans, Bernard J. E.
Fabian, Joseph M.
O’Carroll, David C.
Wiederman, Steven D.
author_sort Lancer, Benjamin H.
collection PubMed
description The ability to pursue targets in visually cluttered and distraction-rich environments is critical for predators such as dragonflies. Previously, we identified Centrifugal Small-Target Motion Detector 1 (CSTMD1), a dragonfly visual neuron likely involved in such target-tracking behaviour. CSTMD1 exhibits facilitated responses to targets moving along a continuous trajectory. Moreover, CSTMD1 competitively selects a single target out of a pair. Here, we conducted in vivo, intracellular recordings from CSTMD1 to examine the interplay between facilitation and selection, in response to the presentation of paired targets. We find that neuronal responses to both individual trajectories of simultaneous, paired targets are facilitated, rather than being constrained to the single, selected target. Additionally, switches in selection elicit suppression which is likely an important attribute underlying target pursuit. However, binocular experiments reveal these results are constrained to paired targets within the same visual hemifield, while selection of a target in one visual hemifield establishes ocular dominance that prevents facilitation or response to contralaterally presented targets. These results reveal that the dragonfly brain preattentively represents more than one target trajectory, to balance between attentional flexibility and resistance against distraction.
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spelling pubmed-93886222022-08-20 Preattentive facilitation of target trajectories in a dragonfly visual neuron Lancer, Benjamin H. Evans, Bernard J. E. Fabian, Joseph M. O’Carroll, David C. Wiederman, Steven D. Commun Biol Article The ability to pursue targets in visually cluttered and distraction-rich environments is critical for predators such as dragonflies. Previously, we identified Centrifugal Small-Target Motion Detector 1 (CSTMD1), a dragonfly visual neuron likely involved in such target-tracking behaviour. CSTMD1 exhibits facilitated responses to targets moving along a continuous trajectory. Moreover, CSTMD1 competitively selects a single target out of a pair. Here, we conducted in vivo, intracellular recordings from CSTMD1 to examine the interplay between facilitation and selection, in response to the presentation of paired targets. We find that neuronal responses to both individual trajectories of simultaneous, paired targets are facilitated, rather than being constrained to the single, selected target. Additionally, switches in selection elicit suppression which is likely an important attribute underlying target pursuit. However, binocular experiments reveal these results are constrained to paired targets within the same visual hemifield, while selection of a target in one visual hemifield establishes ocular dominance that prevents facilitation or response to contralaterally presented targets. These results reveal that the dragonfly brain preattentively represents more than one target trajectory, to balance between attentional flexibility and resistance against distraction. Nature Publishing Group UK 2022-08-18 /pmc/articles/PMC9388622/ /pubmed/35982305 http://dx.doi.org/10.1038/s42003-022-03798-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lancer, Benjamin H.
Evans, Bernard J. E.
Fabian, Joseph M.
O’Carroll, David C.
Wiederman, Steven D.
Preattentive facilitation of target trajectories in a dragonfly visual neuron
title Preattentive facilitation of target trajectories in a dragonfly visual neuron
title_full Preattentive facilitation of target trajectories in a dragonfly visual neuron
title_fullStr Preattentive facilitation of target trajectories in a dragonfly visual neuron
title_full_unstemmed Preattentive facilitation of target trajectories in a dragonfly visual neuron
title_short Preattentive facilitation of target trajectories in a dragonfly visual neuron
title_sort preattentive facilitation of target trajectories in a dragonfly visual neuron
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388622/
https://www.ncbi.nlm.nih.gov/pubmed/35982305
http://dx.doi.org/10.1038/s42003-022-03798-8
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