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‘Boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton

Rapid virus proliferation can exert a powerful control on phytoplankton host populations, playing a significant role in marine biogeochemistry and ecology. We explore how marine lytic viruses impact phytoplankton succession, affecting host and nonhost populations. Using an in silico food web we cond...

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Detalles Bibliográficos
Autores principales: Flynn, Kevin J., Mitra, Aditee, Wilson, William H., Kimmance, Susan A., Clark, Darren R., Pelusi, Angela, Polimene, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313554/
https://www.ncbi.nlm.nih.gov/pubmed/35179778
http://dx.doi.org/10.1111/nph.18042
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author Flynn, Kevin J.
Mitra, Aditee
Wilson, William H.
Kimmance, Susan A.
Clark, Darren R.
Pelusi, Angela
Polimene, Luca
author_facet Flynn, Kevin J.
Mitra, Aditee
Wilson, William H.
Kimmance, Susan A.
Clark, Darren R.
Pelusi, Angela
Polimene, Luca
author_sort Flynn, Kevin J.
collection PubMed
description Rapid virus proliferation can exert a powerful control on phytoplankton host populations, playing a significant role in marine biogeochemistry and ecology. We explore how marine lytic viruses impact phytoplankton succession, affecting host and nonhost populations. Using an in silico food web we conducted simulation experiments under a range of different abiotic and biotic conditions, exploring virus–host–grazer interactions and manipulating competition, allometry, motility and cyst cycles. Virus‐host and predator–prey interactions, and interactions with competitors, generate bloom dynamics with a pronounced ‘boom‐and‐busted’ dynamic (BBeD) which leads to the suppression of otherwise potentially successful phytoplankton species. The BBeD is less pronounced at low nutrient loading through distancing of phytoplankton hosts, while high sediment loading and high nonhost biomass decrease the abundance of viruses through adsorption. Larger hosts are inherently more distanced, but motility increases virus attack, while cyst cycles promote spatial and temporal distancing. Virus control of phytoplankton bloom development appears more important than virus‐induced termination of those blooms. This affects plankton succession – not only the growth of species infected by the virus, but also those that compete for the same resources and are collectively subjected to common grazer control. The role of viruses in structuring plankton communities via BBeDs can thus provide an explanation for the paradox of the plankton.
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spelling pubmed-93135542022-07-30 ‘Boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton Flynn, Kevin J. Mitra, Aditee Wilson, William H. Kimmance, Susan A. Clark, Darren R. Pelusi, Angela Polimene, Luca New Phytol Research Rapid virus proliferation can exert a powerful control on phytoplankton host populations, playing a significant role in marine biogeochemistry and ecology. We explore how marine lytic viruses impact phytoplankton succession, affecting host and nonhost populations. Using an in silico food web we conducted simulation experiments under a range of different abiotic and biotic conditions, exploring virus–host–grazer interactions and manipulating competition, allometry, motility and cyst cycles. Virus‐host and predator–prey interactions, and interactions with competitors, generate bloom dynamics with a pronounced ‘boom‐and‐busted’ dynamic (BBeD) which leads to the suppression of otherwise potentially successful phytoplankton species. The BBeD is less pronounced at low nutrient loading through distancing of phytoplankton hosts, while high sediment loading and high nonhost biomass decrease the abundance of viruses through adsorption. Larger hosts are inherently more distanced, but motility increases virus attack, while cyst cycles promote spatial and temporal distancing. Virus control of phytoplankton bloom development appears more important than virus‐induced termination of those blooms. This affects plankton succession – not only the growth of species infected by the virus, but also those that compete for the same resources and are collectively subjected to common grazer control. The role of viruses in structuring plankton communities via BBeDs can thus provide an explanation for the paradox of the plankton. John Wiley and Sons Inc. 2022-03-09 2022-05 /pmc/articles/PMC9313554/ /pubmed/35179778 http://dx.doi.org/10.1111/nph.18042 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Flynn, Kevin J.
Mitra, Aditee
Wilson, William H.
Kimmance, Susan A.
Clark, Darren R.
Pelusi, Angela
Polimene, Luca
‘Boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton
title ‘Boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton
title_full ‘Boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton
title_fullStr ‘Boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton
title_full_unstemmed ‘Boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton
title_short ‘Boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton
title_sort ‘boom‐and‐busted’ dynamics of phytoplankton–virus interactions explain the paradox of the plankton
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313554/
https://www.ncbi.nlm.nih.gov/pubmed/35179778
http://dx.doi.org/10.1111/nph.18042
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