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Algal plankton turn to hunting to survive and recover from end-Cretaceous impact darkness

The end-Cretaceous bolide impact triggered the devastation of marine ecosystems. However, the specific kill mechanism(s) are still debated, and how primary production subsequently recovered remains elusive. We used marine plankton microfossils and eco-evolutionary modeling to determine strategies fo...

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Autores principales: Gibbs, Samantha J., Bown, Paul R., Ward, Ben A., Alvarez, Sarah A., Kim, Hojung, Archontikis, Odysseas A., Sauterey, Boris, Poulton, Alex J., Wilson, Jamie, Ridgwell, Andy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608818/
https://www.ncbi.nlm.nih.gov/pubmed/33127682
http://dx.doi.org/10.1126/sciadv.abc9123
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author Gibbs, Samantha J.
Bown, Paul R.
Ward, Ben A.
Alvarez, Sarah A.
Kim, Hojung
Archontikis, Odysseas A.
Sauterey, Boris
Poulton, Alex J.
Wilson, Jamie
Ridgwell, Andy
author_facet Gibbs, Samantha J.
Bown, Paul R.
Ward, Ben A.
Alvarez, Sarah A.
Kim, Hojung
Archontikis, Odysseas A.
Sauterey, Boris
Poulton, Alex J.
Wilson, Jamie
Ridgwell, Andy
author_sort Gibbs, Samantha J.
collection PubMed
description The end-Cretaceous bolide impact triggered the devastation of marine ecosystems. However, the specific kill mechanism(s) are still debated, and how primary production subsequently recovered remains elusive. We used marine plankton microfossils and eco-evolutionary modeling to determine strategies for survival and recovery, finding that widespread phagotrophy (prey ingestion) was fundamental to plankton surviving the impact and also for the subsequent reestablishment of primary production. Ecological selectivity points to extreme post-impact light inhibition as the principal kill mechanism, with the marine food chain temporarily reset to a bacteria-dominated state. Subsequently, in a sunlit ocean inhabited by only rare survivor grazers but abundant small prey, it was mixotrophic nutrition (autotrophy and heterotrophy) and increasing cell sizes that enabled the eventual reestablishment of marine food webs some 2 million years later.
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spelling pubmed-76088182020-11-13 Algal plankton turn to hunting to survive and recover from end-Cretaceous impact darkness Gibbs, Samantha J. Bown, Paul R. Ward, Ben A. Alvarez, Sarah A. Kim, Hojung Archontikis, Odysseas A. Sauterey, Boris Poulton, Alex J. Wilson, Jamie Ridgwell, Andy Sci Adv Research Articles The end-Cretaceous bolide impact triggered the devastation of marine ecosystems. However, the specific kill mechanism(s) are still debated, and how primary production subsequently recovered remains elusive. We used marine plankton microfossils and eco-evolutionary modeling to determine strategies for survival and recovery, finding that widespread phagotrophy (prey ingestion) was fundamental to plankton surviving the impact and also for the subsequent reestablishment of primary production. Ecological selectivity points to extreme post-impact light inhibition as the principal kill mechanism, with the marine food chain temporarily reset to a bacteria-dominated state. Subsequently, in a sunlit ocean inhabited by only rare survivor grazers but abundant small prey, it was mixotrophic nutrition (autotrophy and heterotrophy) and increasing cell sizes that enabled the eventual reestablishment of marine food webs some 2 million years later. American Association for the Advancement of Science 2020-10-30 /pmc/articles/PMC7608818/ /pubmed/33127682 http://dx.doi.org/10.1126/sciadv.abc9123 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Gibbs, Samantha J.
Bown, Paul R.
Ward, Ben A.
Alvarez, Sarah A.
Kim, Hojung
Archontikis, Odysseas A.
Sauterey, Boris
Poulton, Alex J.
Wilson, Jamie
Ridgwell, Andy
Algal plankton turn to hunting to survive and recover from end-Cretaceous impact darkness
title Algal plankton turn to hunting to survive and recover from end-Cretaceous impact darkness
title_full Algal plankton turn to hunting to survive and recover from end-Cretaceous impact darkness
title_fullStr Algal plankton turn to hunting to survive and recover from end-Cretaceous impact darkness
title_full_unstemmed Algal plankton turn to hunting to survive and recover from end-Cretaceous impact darkness
title_short Algal plankton turn to hunting to survive and recover from end-Cretaceous impact darkness
title_sort algal plankton turn to hunting to survive and recover from end-cretaceous impact darkness
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608818/
https://www.ncbi.nlm.nih.gov/pubmed/33127682
http://dx.doi.org/10.1126/sciadv.abc9123
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