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The role of intra-guild indirect interactions in assembling plant-pollinator networks

Understanding the assembly of plant-pollinator communities has become critical to their conservation given the rise of species invasions, extirpations, and species’ range shifts. Over the course of assembly, colonizer establishment produces core interaction patterns, called motifs, which shape the t...

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Autores principales: Dritz, Sabine, Nelson, Rebecca A., Valdovinos, Fernanda S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507117/
https://www.ncbi.nlm.nih.gov/pubmed/37723167
http://dx.doi.org/10.1038/s41467-023-41508-y
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author Dritz, Sabine
Nelson, Rebecca A.
Valdovinos, Fernanda S.
author_facet Dritz, Sabine
Nelson, Rebecca A.
Valdovinos, Fernanda S.
author_sort Dritz, Sabine
collection PubMed
description Understanding the assembly of plant-pollinator communities has become critical to their conservation given the rise of species invasions, extirpations, and species’ range shifts. Over the course of assembly, colonizer establishment produces core interaction patterns, called motifs, which shape the trajectory of assembling network structure. Dynamic assembly models can advance our understanding of this process by linking the transient dynamics of colonizer establishment to long-term network development. In this study, we investigate the role of intra-guild indirect interactions and adaptive foraging in shaping the structure of assembling plant-pollinator networks by developing: 1) an assembly model that includes population dynamics and adaptive foraging, and 2) a motif analysis tracking the intra-guild indirect interactions of colonizing species throughout their establishment. We find that while colonizers leverage indirect competition for shared mutualistic resources to establish, adaptive foraging maintains the persistence of inferior competitors. This produces core motifs in which specialist and generalist species coexist on shared mutualistic resources which leads to the emergence of nested networks. Further, the persistence of specialists develops richer and less connected networks which is consistent with empirical data. Our work contributes new understanding and methods to study the effects of species’ intra-guild indirect interactions on community assembly.
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spelling pubmed-105071172023-09-20 The role of intra-guild indirect interactions in assembling plant-pollinator networks Dritz, Sabine Nelson, Rebecca A. Valdovinos, Fernanda S. Nat Commun Article Understanding the assembly of plant-pollinator communities has become critical to their conservation given the rise of species invasions, extirpations, and species’ range shifts. Over the course of assembly, colonizer establishment produces core interaction patterns, called motifs, which shape the trajectory of assembling network structure. Dynamic assembly models can advance our understanding of this process by linking the transient dynamics of colonizer establishment to long-term network development. In this study, we investigate the role of intra-guild indirect interactions and adaptive foraging in shaping the structure of assembling plant-pollinator networks by developing: 1) an assembly model that includes population dynamics and adaptive foraging, and 2) a motif analysis tracking the intra-guild indirect interactions of colonizing species throughout their establishment. We find that while colonizers leverage indirect competition for shared mutualistic resources to establish, adaptive foraging maintains the persistence of inferior competitors. This produces core motifs in which specialist and generalist species coexist on shared mutualistic resources which leads to the emergence of nested networks. Further, the persistence of specialists develops richer and less connected networks which is consistent with empirical data. Our work contributes new understanding and methods to study the effects of species’ intra-guild indirect interactions on community assembly. Nature Publishing Group UK 2023-09-18 /pmc/articles/PMC10507117/ /pubmed/37723167 http://dx.doi.org/10.1038/s41467-023-41508-y Text en © The Author(s) 2023 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 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 Article
Dritz, Sabine
Nelson, Rebecca A.
Valdovinos, Fernanda S.
The role of intra-guild indirect interactions in assembling plant-pollinator networks
title The role of intra-guild indirect interactions in assembling plant-pollinator networks
title_full The role of intra-guild indirect interactions in assembling plant-pollinator networks
title_fullStr The role of intra-guild indirect interactions in assembling plant-pollinator networks
title_full_unstemmed The role of intra-guild indirect interactions in assembling plant-pollinator networks
title_short The role of intra-guild indirect interactions in assembling plant-pollinator networks
title_sort role of intra-guild indirect interactions in assembling plant-pollinator networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507117/
https://www.ncbi.nlm.nih.gov/pubmed/37723167
http://dx.doi.org/10.1038/s41467-023-41508-y
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