Bauer Ann M, Li Weiqiang, Rybacki Kyle S, Roden Eric E, Kump Lee R, Johnson Clark M
Department of Geoscience, University of Wisconsin-Madison, Madison, WI 53706.
NASA Astrobiology Institute, Madison, WI 53706.
Proc Natl Acad Sci U S A. 2025 Sep 9;122(36):e2510289122. doi: 10.1073/pnas.2510289122. Epub 2025 Sep 2.
Redox-sensitive elements figure prominently in studies of the evolution of Earth's surface redox state, including the first major rise in atmospheric O, the Paleoproterozoic Great Oxidation Event. Most Precambrian rocks endured multistage tectonothermal histories, however, adding ambiguity to interpretation of their chemistry. Here, we apply U-Th-Pb isotope geochronology to the highly oxidized ~2.06 Ga Kuetsjärvi Volcanic Formation, Pechenga Greenstone Belt, Russia, to constrain the age and extent of U oxidation. By contrasting the relative mobility of U and Th using Pb isotopes, we find that complete to near-complete oxidation and removal of U occurred shortly after eruption. We argue that this likely indicates relatively high atmospheric O, where oxidative weathering and alteration produced a global pulse of U to the oceans. Such a pulse could explain widespread shifts in the U-Th-Pb isotope character of mantle reservoirs at ~2 Ga, including a decrease in the Th/U ratio of the mid-ocean ridge basalt source and inception of the high-U/Pb (HIMU) source to ocean island basalts, underscoring the connections between the redox character of the Paleoproterozoic surface and deep Earth. Using Pb-Pb, U-Pb, U-Pb, and Th-Pb geochronology, ~2.06 Ga oxidative loss of U may be distinguished from reintroduction of U at ~1.8 Ga during regional metamorphism, as well as Pb loss during a Phanerozoic tectonothermal event. Our results therefore establish the complex history of redox-sensitive element behavior in the rocks, highlighting the fact that elemental abundances, by themselves, are unlikely to capture straightforward proxy information in rocks that have seen multistage geologic histories.
氧化还原敏感元素在地球表面氧化还原状态演化的研究中占据显著地位,包括大气中氧气的首次大幅上升,即古元古代大氧化事件。然而,大多数前寒武纪岩石经历了多阶段的构造热历史,这给它们化学性质的解释增添了模糊性。在此,我们将铀 - 钍 - 铅同位素地质年代学应用于俄罗斯佩琴加绿岩带高度氧化的约20.6亿年库埃茨järvi火山岩组,以确定铀氧化的年龄和范围。通过利用铅同位素对比铀和钍的相对迁移率,我们发现喷发后不久铀就发生了完全至近乎完全的氧化和去除。我们认为,这可能表明大气中的氧气含量相对较高,在这种情况下,氧化风化和蚀变作用向海洋输送了全球性的铀脉冲。这样的脉冲可以解释约20亿年前地幔储库铀 - 钍 - 铅同位素特征的广泛变化,包括大洋中脊玄武岩源区钍/铀比值的降低以及海洋岛弧玄武岩高铀/铅(HIMU)源区的形成,强调了古元古代地表与地球深部氧化还原特征之间的联系。利用铅 - 铅、铀 - 铅、铀 - 铅和钍 - 铅地质年代学,可以将约20.6亿年的铀氧化损失与约18亿年区域变质作用期间铀的重新引入以及显生宙构造热事件期间铅的损失区分开来。因此,我们的研究结果确定了岩石中氧化还原敏感元素行为的复杂历史,突出了这样一个事实,即对于经历了多阶段地质历史的岩石,元素丰度本身不太可能获取直接的代理信息。