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Parallel motion vision pathways in the brain of a tropical bee
Spatial orientation is a prerequisite for most behaviors. In insects, the underlying neural computations take place in the central complex (CX), the brain’s navigational center. In this region different streams of sensory information converge to enable context-dependent navigational decisions. Accor...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354172/ https://www.ncbi.nlm.nih.gov/pubmed/37017717 http://dx.doi.org/10.1007/s00359-023-01625-x |
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author | Honkanen, Anna Hensgen, Ronja Kannan, Kavitha Adden, Andrea Warrant, Eric Wcislo, William Heinze, Stanley |
author_facet | Honkanen, Anna Hensgen, Ronja Kannan, Kavitha Adden, Andrea Warrant, Eric Wcislo, William Heinze, Stanley |
author_sort | Honkanen, Anna |
collection | PubMed |
description | Spatial orientation is a prerequisite for most behaviors. In insects, the underlying neural computations take place in the central complex (CX), the brain’s navigational center. In this region different streams of sensory information converge to enable context-dependent navigational decisions. Accordingly, a variety of CX input neurons deliver information about different navigation-relevant cues. In bees, direction encoding polarized light signals converge with translational optic flow signals that are suited to encode the flight speed of the animals. The continuous integration of speed and directions in the CX can be used to generate a vector memory of the bee’s current position in space in relation to its nest, i.e., perform path integration. This process depends on specific, complex features of the optic flow encoding CX input neurons, but it is unknown how this information is derived from the visual periphery. Here, we thus aimed at gaining insight into how simple motion signals are reshaped upstream of the speed encoding CX input neurons to generate their complex features. Using electrophysiology and anatomical analyses of the halictic bees Megalopta genalis and Megalopta centralis, we identified a wide range of motion-sensitive neurons connecting the optic lobes with the central brain. While most neurons formed pathways with characteristics incompatible with CX speed neurons, we showed that one group of lobula projection neurons possess some physiological and anatomical features required to generate the visual responses of CX optic-flow encoding neurons. However, as these neurons cannot explain all features of CX speed cells, local interneurons of the central brain or alternative input cells from the optic lobe are additionally required to construct inputs with sufficient complexity to deliver speed signals suited for path integration in bees. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00359-023-01625-x. |
format | Online Article Text |
id | pubmed-10354172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-103541722023-07-20 Parallel motion vision pathways in the brain of a tropical bee Honkanen, Anna Hensgen, Ronja Kannan, Kavitha Adden, Andrea Warrant, Eric Wcislo, William Heinze, Stanley J Comp Physiol A Neuroethol Sens Neural Behav Physiol Original Paper Spatial orientation is a prerequisite for most behaviors. In insects, the underlying neural computations take place in the central complex (CX), the brain’s navigational center. In this region different streams of sensory information converge to enable context-dependent navigational decisions. Accordingly, a variety of CX input neurons deliver information about different navigation-relevant cues. In bees, direction encoding polarized light signals converge with translational optic flow signals that are suited to encode the flight speed of the animals. The continuous integration of speed and directions in the CX can be used to generate a vector memory of the bee’s current position in space in relation to its nest, i.e., perform path integration. This process depends on specific, complex features of the optic flow encoding CX input neurons, but it is unknown how this information is derived from the visual periphery. Here, we thus aimed at gaining insight into how simple motion signals are reshaped upstream of the speed encoding CX input neurons to generate their complex features. Using electrophysiology and anatomical analyses of the halictic bees Megalopta genalis and Megalopta centralis, we identified a wide range of motion-sensitive neurons connecting the optic lobes with the central brain. While most neurons formed pathways with characteristics incompatible with CX speed neurons, we showed that one group of lobula projection neurons possess some physiological and anatomical features required to generate the visual responses of CX optic-flow encoding neurons. However, as these neurons cannot explain all features of CX speed cells, local interneurons of the central brain or alternative input cells from the optic lobe are additionally required to construct inputs with sufficient complexity to deliver speed signals suited for path integration in bees. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00359-023-01625-x. Springer Berlin Heidelberg 2023-04-05 2023 /pmc/articles/PMC10354172/ /pubmed/37017717 http://dx.doi.org/10.1007/s00359-023-01625-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Honkanen, Anna Hensgen, Ronja Kannan, Kavitha Adden, Andrea Warrant, Eric Wcislo, William Heinze, Stanley Parallel motion vision pathways in the brain of a tropical bee |
title | Parallel motion vision pathways in the brain of a tropical bee |
title_full | Parallel motion vision pathways in the brain of a tropical bee |
title_fullStr | Parallel motion vision pathways in the brain of a tropical bee |
title_full_unstemmed | Parallel motion vision pathways in the brain of a tropical bee |
title_short | Parallel motion vision pathways in the brain of a tropical bee |
title_sort | parallel motion vision pathways in the brain of a tropical bee |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354172/ https://www.ncbi.nlm.nih.gov/pubmed/37017717 http://dx.doi.org/10.1007/s00359-023-01625-x |
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