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Rapid timescale for an oxic transition during the Great Oxidation Event and the instability of low atmospheric O
by
Zahnle, Kevin J.
, Claire, Mark W.
, Wogan, Nicholas F.
, Catling, David C.
2022
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Rapid timescale for an oxic transition during the Great Oxidation Event and the instability of low atmospheric O
by
Zahnle, Kevin J.
, Claire, Mark W.
, Wogan, Nicholas F.
, Catling, David C.
2022
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Rapid timescale for an oxic transition during the Great Oxidation Event and the instability of low atmospheric O
Journal Article
Rapid timescale for an oxic transition during the Great Oxidation Event and the instability of low atmospheric O
2022
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Overview
The Great Oxidation Event (GOE), arguably the most important event to occur on Earth since the origin of life, marks the time when an oxygen-rich atmosphere first appeared. However, it is not known whether the change was abrupt and permanent or fitful and drawn out over tens or hundreds of millions of years. Here, we developed a one-dimensional time-dependent photochemical model to resolve time-dependent behavior of the chemically unstable transitional atmosphere as it responded to changes in biogenic forcing. When forced with step-wise changes in biogenic fluxes, transitions between anoxic and oxic atmospheres take between only 10² and 10⁵ y. Results also suggest that O₂ between ∼10−8 and ∼10−4 mixing ratio is unstable to plausible atmospheric perturbations. For example, when atmospheres with these O₂ concentrations experience fractional variations in the surface CH₄ flux comparable to those caused by modern Milankovich cycling, oxygen fluctuates between anoxic (∼10−8) and oxic (∼10−4) mixing ratios. Overall, our simulations are consistent with possible geologic evidence of unstable atmospheric O₂, after initial oxygenation, which could occasionally collapse from changes in biospheric or volcanic fluxes. Additionally, modeling favors mid- Proterozoic O₂ exceeding 10−4 to 10−3 mixing ratio; otherwise, O₂ would periodically fall below 10−7 mixing ratio, which would be inconsistent with post-GOE absence of sulfur isotope mass-independent fractionation.
Publisher
National Academy of Sciences
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