V13A-4753:
Characterization of Possible Carbonatites in Southeast Missouri
Monday, 15 December 2014
Ethan J Shavers1,2, Abuduwasiti Wulamu1, John P Encarnacion2 and Patrick B Luetkemeyer2, (1)Saint Louis University, Center for Sustainability, Saint Louis, MO, United States, (2)Saint Louis University, Department of Earth and Atmospheric Sciences, Saint Louis, MO, United States
Abstract:
Carbonatite is an igneous rock containing greater than 50% carbonate minerals. These rocks are the most common host of REE mineralization and may contain other economic deposits such as uranium, fluorine and niobium. Several researchers have mentioned the presence of a carbonatite phase interspersed among the olivine melilitite-alnöite dikes and diatremes of southeast Missouri, yet a comprehensive validation of this occurrence has, so far, remained elusive. Here we present petrographic, cathodoluminescence, stable isotope and Vis-NIR analysis which support the presence of a carbonatite magma. We identify apparently single generation calcite groundmass surrounding country rock xenoliths and olivine-cored mafic spheroids altered to carbonate and opaque minerals. We present stable isotope data for twenty samples of intrusive and country rock from across the study area. δ18O values for all rock types exhibit little variation with values between 21.9 ‰ and 28.1 ‰ (VSMOW), possibly the result of outgassing during emplacement. Measured δ13C values of (1) carbonate country rocks are between -0.1 ‰ and -2.9 ‰ (VPDB), (2) ultramafic and carbonate-rich mafic rocks range from -3.0 ‰ to -4.6 ‰ (VPDB) and (3) carbonate-rich rocks with volcanic textures, as well as carbonate veins within mafic rocks, fall between -5.4 ‰ to -8.2 ‰ (VPDB). We suggest that this data and initial petrographic observations indicate (1) limited fluid-rock interaction as the host rock clasts have retained their original isotopic signature, (2) an initial ultramafic phase enriched in 13C by a small amount of sedimentary rock due to low initial C content, (3) mantle sourced carbonate fluids entraining fragments of the ultramafic phase and xenoliths. However, future electron microprobe studies may allow us to further constrain the causes for the observed isotopic shifts. We compare laboratory reflectance measurements of a dolomitic intrusive and adjacent dolomite country rock. Absorption bands in the 0.42-1.35 and 2.2-2.4 µm regions indicate unique Si, Fe, Mg, Al and possibly Cr mineralization in the intrusive rock. These features may indicate higher chemical content in addition to, or alternately, intrusive specific mineralogy. This data may allow for future carbonatite identification using remote imaging spectroscopy.