Co‐culture with Synechococcus facilitates growth of Prochlorococcus under ocean acidification conditions

Summary Anthropogenic CO 2 emissions are projected to lower the pH of the ocean 0.3 units by 2100. Previous studies suggested that Prochlorococcus and Synechococcus , the numerically dominant phytoplankton in the oceans, have different responses to elevated CO 2 that may result in a dramatic shift i...

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Bibliographic Details
Published in:Environmental Microbiology
Main Authors: Knight, Margaret A., Morris, J. Jeffrey
Other Authors: National Science Foundation, Simons Foundation
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2020
Subjects:
Online Access:http://dx.doi.org/10.1111/1462-2920.15277
https://onlinelibrary.wiley.com/doi/pdf/10.1111/1462-2920.15277
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/1462-2920.15277
https://sfamjournals.onlinelibrary.wiley.com/doi/am-pdf/10.1111/1462-2920.15277
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Summary:Summary Anthropogenic CO 2 emissions are projected to lower the pH of the ocean 0.3 units by 2100. Previous studies suggested that Prochlorococcus and Synechococcus , the numerically dominant phytoplankton in the oceans, have different responses to elevated CO 2 that may result in a dramatic shift in their relative abundances in future oceans. Here we showed that the exponential growth rates of these two genera respond to future CO 2 conditions in a manner similar to other cyanobacteria, but Prochlorococcus strains had significantly lower realized growth rates under elevated CO 2 regimes due to poor survival after exposure to fresh culture media. Despite this, a Synechococcus strain was unable to outcompete a Prochlorococcus strain in co‐culture at elevated CO 2 . Under these conditions, Prochlorococcus ' poor response to elevated CO 2 disappeared, and Prochlorococcus' relative fitness showed negative frequency dependence, with both competitors having significant fitness advantages when initially rare. These experiments suggested that the two strains should be able to coexist indefinitely in co‐culture despite sharing nearly identical nutritional requirements. We speculate that negative frequency dependence exists due to reductive Black Queen evolution that has resulted in a passively mutualistic relationship analogous to that connecting Prochlorococcus with the ‘helper’ heterotrophic microbes in its environment.