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      High pCO 2-induced exopolysaccharide-rich ballasted aggregates of planktonic cyanobacteria could explain Paleoproterozoic carbon burial

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          Abstract

          The contribution of planktonic cyanobacteria to burial of organic carbon in deep-sea sediments before the emergence of eukaryotic predators ~1.5 Ga has been considered negligible owing to the slow sinking speed of their small cells. However, global, highly positive excursion in carbon isotope values of inorganic carbonates ~2.22–2.06 Ga implies massive organic matter burial that had to be linked to oceanic cyanobacteria. Here to elucidate that link, we experiment with unicellular planktonic cyanobacteria acclimated to high partial CO 2 pressure ( pCO 2) representative of the early Paleoproterozoic. We find that high pCO 2 boosts generation of acidic extracellular polysaccharides (EPS) that adsorb Ca and Mg cations, support mineralization, and aggregate cells to form ballasted particles. The down flux of such self-assembled cyanobacterial aggregates would decouple the oxygenic photosynthesis from oxidative respiration at the ocean scale, drive export of organic matter from surface to deep ocean and sustain oxygenation of the planetary surface.

          Abstract

          A Paleoproterozoic carbon isotope anomaly is likely linked to burial of oceanic cyanobacteria, but it is not clear how burial occurred. Here, the authors find that, under Paleoproterozoic pCO 2 conditions, planktonic cyanobacteria increase exopolysaccharide production and mineralization, leading to aggregation and faster sinking.

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          Most cited references57

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          Evolution of the nitrogen cycle and its influence on the biological sequestration of CO2 in the ocean

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            Earth's early atmosphere.

            J. Kasting (1993)
            Ideas about atmospheric composition and climate on the early Earth have evolved considerably over the last 30 years, but many uncertainties still remain. It is generally agreed that the atmosphere contained little or no free oxygen initially and that oxygen concentrations increased markedly near 2.0 billion years ago, but the precise timing of and reasons for its rise remain unexplained. Likewise, it is usually conceded that the atmospheric greenhouse effect must have been higher in the past to offset reduced solar luminosity, but the levels of atmospheric carbon dioxide and other greenhouse gases required remain speculative. A better understanding of past atmospheric evolution is important to understanding the evolution of life and to predicting whether Earth-like planets might exist elsewhere in the galaxy.
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              Dating the rise of atmospheric oxygen.

              Several lines of geological and geochemical evidence indicate that the level of atmospheric oxygen was extremely low before 2.45 billion years (Gyr) ago, and that it had reached considerable levels by 2.22 Gyr ago. Here we present evidence that the rise of atmospheric oxygen had occurred by 2.32 Gyr ago. We found that syngenetic pyrite is present in organic-rich shales of the 2.32-Gyr-old Rooihoogte and Timeball Hill formations, South Africa. The range of the isotopic composition of sulphur in this pyrite is large and shows no evidence of mass-independent fractionation, indicating that atmospheric oxygen was present at significant levels (that is, greater than 10(-5) times that of the present atmospheric level) during the deposition of these units. The presence of rounded pebbles of sideritic iron formation at the base of the Rooihoogte Formation and an extensive and thick ironstone layer consisting of haematitic pisolites and oölites in the upper Timeball Hill Formation indicate that atmospheric oxygen rose significantly, perhaps for the first time, during the deposition of the Rooihoogte and Timeball Hill formations. These units were deposited between what are probably the second and third of the three Palaeoproterozoic glacial events.

                Author and article information

                Contributors
                nkamennaya@tauex.tau.ac.il
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                29 May 2018
                29 May 2018
                2018
                : 9
                : 2116
                Affiliations
                [1 ]ISNI 0000 0001 2231 4551, GRID grid.184769.5, Earth Sciences Division, , Lawrence Berkeley National Laboratory (LBNL), ; Berkeley, CA 94720 USA
                [2 ]ISNI 0000 0001 2231 4551, GRID grid.184769.5, Molecular Biophysics and Integrated Bioimaging Sciences Division, , LBNL, ; Berkeley, CA 94720 USA
                [3 ]ISNI 0000 0001 2181 7878, GRID grid.47840.3f, Department of Chemistry, , University of California, ; Berkeley, CA 94720 USA
                [4 ]ISNI 0000 0001 2231 4551, GRID grid.184769.5, The Molecular Foundry, , LBNL, ; Berkeley, CA 94720 USA
                [5 ]ISNI 0000 0004 1937 0546, GRID grid.12136.37, Present Address: School of Plant Sciences and Food Security, The George S. Wise Faculty of Life Sciences, , Tel Aviv University, ; Tel Aviv, 6997801 Israel
                [6 ]ISNI 0000 0001 2218 3491, GRID grid.451303.0, Present Address: The Environmental Molecular Sciences Laboratory, , Pacific Northwest National Laboratory, ; P.O Box 999, K8-93, Richland, WA 99352 USA
                Author information
                http://orcid.org/0000-0001-8909-6712
                Article
                4588
                10.1038/s41467-018-04588-9
                5974010
                29844378
                425716ee-fb55-47e1-a97d-75a0bf2c0d29
                © The Author(s) 2018

                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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 5 December 2014
                : 13 April 2018
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