Method Summary:Rocks were collected from either drill core or surface outcrop without obvious weathering. Exterior surfaces were removed. Samples were powdered in a tungsten carbide mill from chips that were picked to avoid veins. Major element concentrations were determined using either an ICP-MS (Agilent 7500ce Series, or Thermo Element2) or an ICP-AES (Iris Advantage) after a three-acid dissolution or a metaborate fusion, respectively. Accuracy and precision for major element analyses was based on duplicates of the geostandards IF-G, SDO-1, and BHVO-1, and estimated error is less than 5%. For Mo isotopes, powdered samples were digested with concentrated HNO 3 + HF and HNO 3 + HCl, and then the samples were evaporated and dissolved with 7 mol/L HCl.

The oxygen content of Earth's atmosphere has varied greatly through time, progressing from exceptionally low levels before about 2.3 billion years ago, to much higher levels afterward. In the absence of better information, we usually view the progress in Earth's oxygenation as a series of steps followed by periods of relative stasis. In contrast to this view, and as reported here, a dynamic evolution of Earth's oxygenation is recorded in ancient sediments from the Republic of Gabon from between about 2,150 and 2,080 million years ago. The oldest sediments in this sequence were deposited in well-oxygenated deep waters whereas the youngest were deposited in euxinic waters, which were globally extensive. These fluctuations in oxygenation were likely driven by the comings and goings of the Lomagundi carbon isotope excursion, the longest-lived positive δ 13 C excursion in Earth history, generating a huge oxygen source to the atmosphere. As the Lomagundi event waned, the oxygen source became a net oxygen sink as Lomagundi organic matter became oxidized, driving oxygen to low levels; this state may have persisted for 200 million years.GOE | Paleoproterozoic | marine chemistry | Mo isotope | trace metal

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