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Tuneable reflexes control antennal positioning in flying hawkmoths

Complex behaviours may be viewed as sequences of modular actions, each elicited by specific sensory cues in their characteristic timescales. From this perspective, we can construct models in which unitary behavioural modules are hierarchically placed in context of related actions. Here, we analyse a...

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Autores principales: Natesan, Dinesh, Saxena, Nitesh, Ekeberg, Örjan, Sane, Sanjay P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898381/
https://www.ncbi.nlm.nih.gov/pubmed/31811150
http://dx.doi.org/10.1038/s41467-019-13595-3
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author Natesan, Dinesh
Saxena, Nitesh
Ekeberg, Örjan
Sane, Sanjay P.
author_facet Natesan, Dinesh
Saxena, Nitesh
Ekeberg, Örjan
Sane, Sanjay P.
author_sort Natesan, Dinesh
collection PubMed
description Complex behaviours may be viewed as sequences of modular actions, each elicited by specific sensory cues in their characteristic timescales. From this perspective, we can construct models in which unitary behavioural modules are hierarchically placed in context of related actions. Here, we analyse antennal positioning reflex in hawkmoths as a tuneable behavioural unit. Mechanosensory feedback from two antennal structures, Böhm’s bristles (BB) and Johnston’s organs (JO), determines antennal position. At flight onset, antennae attain a specific position, which is maintained by feedback from BB. Simultaneously, JO senses deflections in flagellum-pedicel joint due to frontal airflow, to modulate its steady-state position. Restricting JO abolishes positional modulation but maintains stability against perturbations. Linear feedback models are sufficient to predict antennal dynamics at various set-points. We modelled antennal positioning as a hierarchical neural-circuit in which fast BB feedback maintains instantaneous set-point, but slow JO feedback modulates it, thereby elucidating mechanisms underlying its robustness and flexibility.
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spelling pubmed-68983812019-12-09 Tuneable reflexes control antennal positioning in flying hawkmoths Natesan, Dinesh Saxena, Nitesh Ekeberg, Örjan Sane, Sanjay P. Nat Commun Article Complex behaviours may be viewed as sequences of modular actions, each elicited by specific sensory cues in their characteristic timescales. From this perspective, we can construct models in which unitary behavioural modules are hierarchically placed in context of related actions. Here, we analyse antennal positioning reflex in hawkmoths as a tuneable behavioural unit. Mechanosensory feedback from two antennal structures, Böhm’s bristles (BB) and Johnston’s organs (JO), determines antennal position. At flight onset, antennae attain a specific position, which is maintained by feedback from BB. Simultaneously, JO senses deflections in flagellum-pedicel joint due to frontal airflow, to modulate its steady-state position. Restricting JO abolishes positional modulation but maintains stability against perturbations. Linear feedback models are sufficient to predict antennal dynamics at various set-points. We modelled antennal positioning as a hierarchical neural-circuit in which fast BB feedback maintains instantaneous set-point, but slow JO feedback modulates it, thereby elucidating mechanisms underlying its robustness and flexibility. Nature Publishing Group UK 2019-12-06 /pmc/articles/PMC6898381/ /pubmed/31811150 http://dx.doi.org/10.1038/s41467-019-13595-3 Text en © The Author(s) 2019 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/.
spellingShingle Article
Natesan, Dinesh
Saxena, Nitesh
Ekeberg, Örjan
Sane, Sanjay P.
Tuneable reflexes control antennal positioning in flying hawkmoths
title Tuneable reflexes control antennal positioning in flying hawkmoths
title_full Tuneable reflexes control antennal positioning in flying hawkmoths
title_fullStr Tuneable reflexes control antennal positioning in flying hawkmoths
title_full_unstemmed Tuneable reflexes control antennal positioning in flying hawkmoths
title_short Tuneable reflexes control antennal positioning in flying hawkmoths
title_sort tuneable reflexes control antennal positioning in flying hawkmoths
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898381/
https://www.ncbi.nlm.nih.gov/pubmed/31811150
http://dx.doi.org/10.1038/s41467-019-13595-3
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