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NARROW
GeoRef Subject
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all geography including DSDP/ODP Sites and Legs
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North America
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Brazil
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geologic age
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Primary terms
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isotopes
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Mesozoic
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Cretaceous
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metals
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manganese (1)
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North America
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paleoclimatology (4)
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South America
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Brazil
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United States
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Arizona
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Pinal County Arizona (1)
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Kansas
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Douglas County Kansas (1)
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Thomas County Kansas (1)
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Utah
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Wyoming
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Park County Wyoming
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sedimentary rocks
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sedimentary structures
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burrows (7)
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sedimentary structures
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rhizoliths (3)
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sediments
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soils
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soils
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Maastrichtian atmospheric p CO 2 and climatic reconstruction from carbonate paleosols of the Marília Formation (southeastern Brazil)
PALEOENVIRONMENTAL AND PALEOGEOGRAPHIC IMPLICATIONS OF PALEOSOLS AND ICHNOFOSSILS IN THE UPPER PENNSYLVANIAN HALGAITO FORMATION, SOUTHEASTERN UTAH
NEOICHNOLOGY OF SEMIARID ENVIRONMENTS: SOILS AND BURROWING ANIMALS OF THE SONORAN DESERT, ARIZONA, U.S.A.
Discovery of Paleogene Deposits of the Central High Plains Aquifer In the Western Great Plains, U.S.A.
Geochemical Recharge Estimation and the Effects of a Declining Water Table
MANGANESE-BEARING RHIZOCRETIONS IN THE WILLWOOD FORMATION, WYOMING, U.S.A.: IMPLICATIONS FOR PALEOCLIMATE DURING THE PALEOCENE–EOCENE THERMAL MAXIMUM
Abstract Pedogenic siderite is a carbonate mineral that forms in the reducing groundwaters of poorly drained soils and paleosols in zonal climatic belts with strongly positive precipitation–evaporation balances. Microcrystalline and spherulitic forms of siderite are commonly recognized in micromorphologic studies of hydromorphic paleosols. Ancient paleosol sphaerosiderites commonly occur with diameters in excess of 1 mm, while modern pedogenic siderite crystal dimensions in excess of 100 µm are rare. Pedogenic siderites have been widely reported from Late Paleozoic, Mesozoic, and Cenozoic paleosols. The carbon and oxygen isotopic compositions of pedogenic siderites have been widely used as proxies for the oxygen isotopic composition of paleoprecipitation for their respective paleosols. Modern process studies of historic pedogenic siderites are yielding a more refined understanding of the stable isotopic systematics of low-temperature siderite. These works will lead to a future change in usage of published siderite–water 18 O fractionation equations.