4.6 Article

High Spatial Resolution U-Pb Geochronology and Pb Isotope Geochemistry of Magnetite-Apatite Ore from the Pea Ridge Iron Oxide-Apatite Deposit, St. Francois Mountains, Southeast Missouri, USA

Journal

ECONOMIC GEOLOGY
Volume 111, Issue 8, Pages 1915-1933

Publisher

SOC ECONOMIC GEOLOGISTS, INC
DOI: 10.2113/econgeo.111.8.1915

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The Pea Ridge iron oxide-apatite (IOA) deposit is one of the major rhyolite-hosted magnetite deposits of the St. Francois Mountains terrane, which is located within the Mesoproterozoic (1.5-1.3 Ga) Granite-Rhyolite province in the U.S. Midcontinent. Precise and accurate determination of the timing and duration of ore-forming processes in this deposit is crucial for understanding its origin and placing it within a deposit-scale and regional geologic context. Apatite and monazite, well-established U-Pb mineral geochronometers, are abundant in the Pea Ridge orebody. However, the potential presence of multiple generations of dateable minerals, processes of dissolution-reprecipitation, and occurrence of micrometer-sized intergrowths and inclusions complicate measurements and interpretations of the geochronological results. Here, we employ a combination of several techniques, including ID-TIMS and high spatial resolution geochronology of apatite and monazite using LA-SC-ICPMS and SHRIMP, and Pb isotope geochemistry of pyrite and magnetite to obtain the first direct age constraints on the formation and alteration history of the Pea Ridge IOA deposit. The oldest apatite TIMS Pb-207*/Pb-206* dates are 1471 +/- 1 and 1468 +/- 1 Ma, slightly younger than (but within error of) the similar to 1474 to similar to 1473 Ma U-Pb zircon ages of the host rhyolites. Dating of apatite and monazite inclusions within apatite provides evidence for at least one younger metasomatic event at similar to 1.44 Ga, and possibly multiple superimposed metasomatic events between 1.47 and 1.44 Ga. Lead isotop analyses of pyrite show extremely radiogenic Pb-206/Pb-204 ratios up to similar to 80 unsupported by in situ U decay. This excess radiogenic Pb in pyrite may have been derived from the spatially associated apatite as apatite recrystallized several tens of million years after its formation. The low initial 206Pb/204Pb ratio of similar to 16.5 and Pb-207/Pb-204 ratio of similar to 15.4 for individual magnetite grains indicate closed U-Pb system behavior in this mineral and are consistent with derivation of the Pb from a mantle-like source.

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