首页期刊导航|Chemical geology
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Chemical geology
Elsevier
Chemical geology

Elsevier

0009-2541

Chemical geology/Journal Chemical geologySCIISTPAHCIEI
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    Paleoproterozoic manganese oxide precipitation in oxic seawater surface and reductive enrichment in anoxic seafloor

    dos Santos, Felipe HolandaAmaral, Wagner da SilvaChi-Fru, ErnestBraga de Souza, Ana Clara...
    17页
    查看更多>>摘要:Accelerated precipitation of Mn-rich rocks in the early Paleoproterozoic ocean is considered to reflect the irreversible rise of oxygen in the atmosphere during the Great Oxidation Event (GOE), 2.501-2.220 billion years ago. But the precipitation conditions, pathways, mechanisms, and linkages to ocean redox, broadly remain unresolved. The Lagoa do Riacho Mn deposit in Borborema Province, northeastern Brazil, Ceara state, consists mainly of manganese-rich and manganese-poor silicates deposited during the GOE epoch. Negative Ce anomalies in the manganese-poor silicates point to the scavenging of Ce3+ onto Mn-oxyhydroxide reactive surfaces in the oxygenated surface waters. In contrast, samples with positive Ce anomalies, predominantly associated with the manganese-rich silicates, indicate a reductive dissolution of Mn-oxyhydroxides across a redoxcline, enriching the anoxic bottom water with Ce and Mn2+. A paleoredox reconstruction based on couple Mn, Mo, and U systematics supports the existence of the proposed Mn-oxide redox shuttle that enriched the anoxic sediment pile with Mn precipitated from the oxygenated shallow surface waters. This study uncovers a unique pathway in Paleoproterozoic Mn mineralization involving the transfer of Mn oxides from an oxygenated upper ocean reservoir to a predominantly deep anoxic silicate reservoir that was subsequently metamorphosed. The proposed Mn oxide sink switch mechanism is different from the commonly reported reductive transfer of Mn to a diagenetic carbonate sink during the Paleoproterozoic.

    Direct dating Paleo-fluid flow events in sedimentary basins

    Yang, PengLiu, KeyuLi, ZhenRankenburg, Kai...
    14页
    查看更多>>摘要:Reconstructing fluid evolution history in old sedimentary basins is extremely challenging due to the prolonged evolution, lack of exact age constraints and absence of preserved fluids. By integrating in-situ calcite U-Pb dating, fluid inclusion analysis, measurements of major and trace elements and carbon-oxygen-strontium isotopes, and molecular composition analysis of petroleum, we have reconstructed the fluid evolution history during the Carboniferous in an Ordovician deeply-buried carbonate reservoir in the Tarim Basin, China, with unprecedented temporal resolution. Five generations of calcite cementation spanning over 37 m.y. are dated in a single calcite vein with U-Pb ages ranging from similar to 353 Ma to similar to 316 Ma. The initial cement was associated with an intrusion of hyper-saline brine, enriched in REEs. This was followed by influx of meteoric water to precipitate the second and third generations of cement, which are characterized by reduced salinity, anomalously high Sr-87/Sr-86 ratios and extremely low concentration of REEs. The fourth generation of calcite cement was formed in a deep-fluid system accompanied by oil charge as indicated by the presence of bitumen, oil inclusions and low delta C-13 and Sr-87/ Sr-86 ratios. The fifth generation of cement was precipitated from equilibrated connate water, and has the lowest salinity and a comparable REE signature to the host rock. Oil charge event occurred around 326 Ma. This study demonstrates the effectiveness of combining in-situ calcite U-Pb geochronology, fluid inclusion analysis, elemental and isotopic geochemistry to elucidate high-resolution temporal fluid evolution in old sedimentary basins with a complex tectonic history, providing a new paradigm for studying geofluid evolution.