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Two-billion-year transitional oxygenation of the Earth’s surface

Author

Listed:
  • Haiyang Wang

    (Chengdu University of Technology
    Nanjing University
    Chengdu University of Technology
    Chengdu University of Technology)

  • Chao Li

    (Chengdu University of Technology
    Chengdu University of Technology
    Chengdu University of Technology)

  • Yongbo Peng

    (Nanjing University)

  • Junpeng Zhang

    (Chinese Academy of Sciences)

  • Meng Cheng

    (Chengdu University of Technology
    Chengdu University of Technology
    Chengdu University of Technology)

  • Xiaobin Cao

    (Nanjing University)

  • Wenkun Qie

    (Chinese Academy of Sciences)

  • Zihu Zhang

    (Chengdu University of Technology
    Chengdu University of Technology
    Chengdu University of Technology)

  • Matthew S. Dodd

    (University of Western Australia)

  • Mingcai Hou

    (Chengdu University of Technology
    Chengdu University of Technology)

  • Malcolm Wallace

    (University of Melbourne)

  • Ashleigh v. S. Hood

    (University of Melbourne)

  • Timothy W. Lyons

    (University of California)

  • Huiming Bao

    (Nanjing University)

Abstract

Earth’s surface underwent stepwise oxygenation before persistently reaching modern levels late in its history1–5, but the details of this transition remain unclear5–16. Here we present a high-resolution 2.5-Gyr record of mass-independent oxygen isotopes in sedimentary sulfate (Δ′17Osulfate), a proxy linked to the atmospheric partial pressure of O2 ( $${p}_{{{\rm{O}}}_{2}}$$ p O 2 )17–19. This record, together with existing sedimentary Δ33S data20–22, demonstrates a 2-Gyr transition characterized by generally low, fluctuating $${p}_{{{\rm{O}}}_{2}}$$ p O 2 between an O2-free state before 2.4 billion years ago (Ga) and a modern $${p}_{{{\rm{O}}}_{2}}$$ p O 2 state after 0.41 Ga, with relatively elevated levels after 1.0 Ga. Our data also show coupled declines in Δ′17Osulfate and sulfate-δ34S during major negative carbonate-δ13C excursions in the Neoproterozoic. Quantitative biogeochemical modelling indicates that these isotopic couplings reflect the increasing $${p}_{{{\rm{O}}}_{2}}$$ p O 2 , which may have driven episodic ocean oxygenation through an increased atmospheric O2 influx. This process intensified the oxidation of marine organics and reduced-sulfur species, while triggering temporary $${p}_{{{\rm{O}}}_{2}}$$ p O 2 drawdowns as negative feedback15. These findings support a dynamic, lengthy co-oxygenation history for the atmosphere and oceans—marked by long-term positive coupling and short-term negative feedbacks—offering a coherent explanation for the anomalous Neoproterozoic carbon cycles23,24 and the protracted, episodic rise of complex life25–27.

Suggested Citation

  • Haiyang Wang & Chao Li & Yongbo Peng & Junpeng Zhang & Meng Cheng & Xiaobin Cao & Wenkun Qie & Zihu Zhang & Matthew S. Dodd & Mingcai Hou & Malcolm Wallace & Ashleigh v. S. Hood & Timothy W. Lyons & H, 2025. "Two-billion-year transitional oxygenation of the Earth’s surface," Nature, Nature, vol. 645(8081), pages 665-671, September.
  • Handle: RePEc:nat:nature:v:645:y:2025:i:8081:d:10.1038_s41586-025-09471-4
    DOI: 10.1038/s41586-025-09471-4
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