Cargando…
Trophic interactions with heterotrophic bacteria limit the range of Prochlorococcus
Prochlorococcus is both the smallest and numerically most abundant photosynthesizing organism on the planet. While thriving in the warm oligotrophic gyres, Prochlorococcus concentrations drop rapidly in higher-latitude regions. Transect data from the North Pacific show the collapse occurring at a wi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764666/ https://www.ncbi.nlm.nih.gov/pubmed/34983874 http://dx.doi.org/10.1073/pnas.2110993118 |
_version_ | 1784634213769674752 |
---|---|
author | Follett, Christopher L. Dutkiewicz, Stephanie Ribalet, François Zakem, Emily Caron, David Armbrust, E. Virginia Follows, Michael J. |
author_facet | Follett, Christopher L. Dutkiewicz, Stephanie Ribalet, François Zakem, Emily Caron, David Armbrust, E. Virginia Follows, Michael J. |
author_sort | Follett, Christopher L. |
collection | PubMed |
description | Prochlorococcus is both the smallest and numerically most abundant photosynthesizing organism on the planet. While thriving in the warm oligotrophic gyres, Prochlorococcus concentrations drop rapidly in higher-latitude regions. Transect data from the North Pacific show the collapse occurring at a wide range of temperatures and latitudes (temperature is often hypothesized to cause this shift), suggesting an ecological mechanism may be at play. An often used size-based theory of phytoplankton community structure that has been incorporated into computational models correctly predicts the dominance of Prochlorococcus in the gyres, and the relative dominance of larger cells at high latitudes. However, both theory and computational models fail to explain the poleward collapse. When heterotrophic bacteria and predators that prey nonspecifically on both Prochlorococcus and bacteria are included in the theoretical framework, the collapse of Prochlorococcus occurs with increasing nutrient supplies. The poleward collapse of Prochlorococcus populations then naturally emerges when this mechanism of “shared predation” is implemented in a complex global ecosystem model. Additionally, the theory correctly predicts trends in both the abundance and mean size of the heterotrophic bacteria. These results suggest that ecological controls need to be considered to understand the biogeography of Prochlorococcus and predict its changes under future ocean conditions. Indirect interactions within a microbial network can be essential in setting community structure. |
format | Online Article Text |
id | pubmed-8764666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-87646662022-01-26 Trophic interactions with heterotrophic bacteria limit the range of Prochlorococcus Follett, Christopher L. Dutkiewicz, Stephanie Ribalet, François Zakem, Emily Caron, David Armbrust, E. Virginia Follows, Michael J. Proc Natl Acad Sci U S A Physical Sciences Prochlorococcus is both the smallest and numerically most abundant photosynthesizing organism on the planet. While thriving in the warm oligotrophic gyres, Prochlorococcus concentrations drop rapidly in higher-latitude regions. Transect data from the North Pacific show the collapse occurring at a wide range of temperatures and latitudes (temperature is often hypothesized to cause this shift), suggesting an ecological mechanism may be at play. An often used size-based theory of phytoplankton community structure that has been incorporated into computational models correctly predicts the dominance of Prochlorococcus in the gyres, and the relative dominance of larger cells at high latitudes. However, both theory and computational models fail to explain the poleward collapse. When heterotrophic bacteria and predators that prey nonspecifically on both Prochlorococcus and bacteria are included in the theoretical framework, the collapse of Prochlorococcus occurs with increasing nutrient supplies. The poleward collapse of Prochlorococcus populations then naturally emerges when this mechanism of “shared predation” is implemented in a complex global ecosystem model. Additionally, the theory correctly predicts trends in both the abundance and mean size of the heterotrophic bacteria. These results suggest that ecological controls need to be considered to understand the biogeography of Prochlorococcus and predict its changes under future ocean conditions. Indirect interactions within a microbial network can be essential in setting community structure. National Academy of Sciences 2022-01-04 2022-01-11 /pmc/articles/PMC8764666/ /pubmed/34983874 http://dx.doi.org/10.1073/pnas.2110993118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Physical Sciences Follett, Christopher L. Dutkiewicz, Stephanie Ribalet, François Zakem, Emily Caron, David Armbrust, E. Virginia Follows, Michael J. Trophic interactions with heterotrophic bacteria limit the range of Prochlorococcus |
title | Trophic interactions with heterotrophic bacteria limit the range of Prochlorococcus |
title_full | Trophic interactions with heterotrophic bacteria limit the range of Prochlorococcus |
title_fullStr | Trophic interactions with heterotrophic bacteria limit the range of Prochlorococcus |
title_full_unstemmed | Trophic interactions with heterotrophic bacteria limit the range of Prochlorococcus |
title_short | Trophic interactions with heterotrophic bacteria limit the range of Prochlorococcus |
title_sort | trophic interactions with heterotrophic bacteria limit the range of prochlorococcus |
topic | Physical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764666/ https://www.ncbi.nlm.nih.gov/pubmed/34983874 http://dx.doi.org/10.1073/pnas.2110993118 |
work_keys_str_mv | AT follettchristopherl trophicinteractionswithheterotrophicbacterialimittherangeofprochlorococcus AT dutkiewiczstephanie trophicinteractionswithheterotrophicbacterialimittherangeofprochlorococcus AT ribaletfrancois trophicinteractionswithheterotrophicbacterialimittherangeofprochlorococcus AT zakememily trophicinteractionswithheterotrophicbacterialimittherangeofprochlorococcus AT carondavid trophicinteractionswithheterotrophicbacterialimittherangeofprochlorococcus AT armbrustevirginia trophicinteractionswithheterotrophicbacterialimittherangeofprochlorococcus AT followsmichaelj trophicinteractionswithheterotrophicbacterialimittherangeofprochlorococcus |