RARE EARTH ELEMENT ZONATION AND FRACTIONATION AT THE BEAR LODGE REE DEPOSIT, WYOMING
Carbonate and fluoride complexes may have been important in fluids precipitating LREE-dominant minerals in the central carbonatites, while phosphate and fluoride complexes may have been important ligands as fluids circulated peripherally. HREEF2+ complexes are less strongly associated than LREEF2+ complexes at hydrothermal temperatures (>150°C), suggesting the fluids cooled below 150°C or that a different ligand, such as phosphate or chloride was involved. Phosphate enrichment in late-stage fluids from carbonatites may be due to dissolution of apatite in carbonatite. An external Paleozoic sedimentary source of phosphate from detrital apatite is also possible.
Complex textural relationships suggest multiple stages of REE precipitation. Parts of the central carbonatites are overprinted by HREE mineralization, often seen as yttrium replacement in parisite. LREE/HREE zonation has recently been discovered between adjacent dikes within individual targets. Electron microprobe data show a similar REE zonation to that observed district-wide (LREE to HREE). Unusual phosphate minerals are zoned from monazite to xenotime compositions.
Stable carbon and oxygen isotope data show a complex history of carbonate and fluorocarbonate crystallization in Bear Lodge carbonatites. Data suggest degassing and low-T alteration were important during carbonatite crystallization and REE-enrichment.