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Windborne migration amplifies insect-mediated pollination services

Worldwide, hoverflies (Syrphidae: Diptera) provide crucial ecosystem services such as pollination and biological pest control. Although many hoverfly species exhibit migratory behavior, the spatiotemporal facets of these movement dynamics, and their ecosystem services implications are poorly underst...

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Autores principales: Jia, Huiru, Liu, Yongqiang, Li, Xiaokang, Li, Hui, Pan, Yunfei, Hu, Chaoxing, Zhou, Xianyong, Wyckhuys, Kris AG, Wu, Kongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042232/
https://www.ncbi.nlm.nih.gov/pubmed/35416148
http://dx.doi.org/10.7554/eLife.76230
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author Jia, Huiru
Liu, Yongqiang
Li, Xiaokang
Li, Hui
Pan, Yunfei
Hu, Chaoxing
Zhou, Xianyong
Wyckhuys, Kris AG
Wu, Kongming
author_facet Jia, Huiru
Liu, Yongqiang
Li, Xiaokang
Li, Hui
Pan, Yunfei
Hu, Chaoxing
Zhou, Xianyong
Wyckhuys, Kris AG
Wu, Kongming
author_sort Jia, Huiru
collection PubMed
description Worldwide, hoverflies (Syrphidae: Diptera) provide crucial ecosystem services such as pollination and biological pest control. Although many hoverfly species exhibit migratory behavior, the spatiotemporal facets of these movement dynamics, and their ecosystem services implications are poorly understood. In this study, we use long-term (16-year) trapping records, trajectory analysis, and intrinsic (i.e., isotope, genetic, pollen) markers to describe migration patterns of the hoverfly Episyrphus balteatus in northern China. Our work reveals how E. balteatus migrate northward during spring–summer and exhibits return (long-range) migration during autumn. The extensive genetic mixing and high genetic diversity of E. balteatus populations underscore its adaptive capacity to environmental disturbances, for example, climate change. Pollen markers and molecular gut analysis further illuminate how E. balteatus visits min. 1012 flowering plant species (39 orders) over space and time. By thus delineating E. balteatus transregional movements and pollination networks, we advance our understanding of its migration ecology and facilitate the design of targeted strategies to conserve and enhance its ecosystem services.
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spelling pubmed-90422322022-04-27 Windborne migration amplifies insect-mediated pollination services Jia, Huiru Liu, Yongqiang Li, Xiaokang Li, Hui Pan, Yunfei Hu, Chaoxing Zhou, Xianyong Wyckhuys, Kris AG Wu, Kongming eLife Ecology Worldwide, hoverflies (Syrphidae: Diptera) provide crucial ecosystem services such as pollination and biological pest control. Although many hoverfly species exhibit migratory behavior, the spatiotemporal facets of these movement dynamics, and their ecosystem services implications are poorly understood. In this study, we use long-term (16-year) trapping records, trajectory analysis, and intrinsic (i.e., isotope, genetic, pollen) markers to describe migration patterns of the hoverfly Episyrphus balteatus in northern China. Our work reveals how E. balteatus migrate northward during spring–summer and exhibits return (long-range) migration during autumn. The extensive genetic mixing and high genetic diversity of E. balteatus populations underscore its adaptive capacity to environmental disturbances, for example, climate change. Pollen markers and molecular gut analysis further illuminate how E. balteatus visits min. 1012 flowering plant species (39 orders) over space and time. By thus delineating E. balteatus transregional movements and pollination networks, we advance our understanding of its migration ecology and facilitate the design of targeted strategies to conserve and enhance its ecosystem services. eLife Sciences Publications, Ltd 2022-04-13 /pmc/articles/PMC9042232/ /pubmed/35416148 http://dx.doi.org/10.7554/eLife.76230 Text en © 2022, Jia et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Ecology
Jia, Huiru
Liu, Yongqiang
Li, Xiaokang
Li, Hui
Pan, Yunfei
Hu, Chaoxing
Zhou, Xianyong
Wyckhuys, Kris AG
Wu, Kongming
Windborne migration amplifies insect-mediated pollination services
title Windborne migration amplifies insect-mediated pollination services
title_full Windborne migration amplifies insect-mediated pollination services
title_fullStr Windborne migration amplifies insect-mediated pollination services
title_full_unstemmed Windborne migration amplifies insect-mediated pollination services
title_short Windborne migration amplifies insect-mediated pollination services
title_sort windborne migration amplifies insect-mediated pollination services
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042232/
https://www.ncbi.nlm.nih.gov/pubmed/35416148
http://dx.doi.org/10.7554/eLife.76230
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