REE Geochemical Characteristics of the Huri Karst-Type Bauxite Deposit, Irano-Himalayan Belt, Northwestern Iran

The Huri bauxite deposit is located 40 km northwest of Maragheh City, East Azerbaijan province, northwestern Iran. Bauxite horizons at Huri develop within karstic depressions and sinkholes of carbonate footwalls of the Ruteh Formation, overlain by carbonate of the Elika Formation. Powder X-ray diffraction (PXRD) and scanning electron microscope, coupled with energy dispersive X-ray spectroscopy (SEM-EDS) analyses show that the Huri bauxite ores consist of hematite, diaspore, kaolinite, and lesser amounts of halloysite, pyrophyllite, illite, goethite, clinochlore, amesite, rutile, zircon, and monazite. Based on geochemical studies (Eu/Eu* vs. Sm/Nd and U/Th bivariate diagrams), basalt rocks interbedded in limestone of the Ruteh Formation are the possible precursor rocks of the Huri bauxite deposit. The pH variations of weathering solutions, fluctuations in the groundwater table level, the function of carbonate bedrock as a geochemical barrier, simultaneous precipitation of Fe-bearing minerals, and preferential scavenging of light rare earth elements (LREE) by hematite played an important role in the fractionation of LREE from heavy rare earth elements (HREE) in the Huri bauxite ores. Fluctuations in groundwater table level, increasing pH of acidic solutions percolating downward, preferential adsorption of Ce onto hematite at the base of the profile, and the possible presence of Ce-bearing fluorocarbonates played an important role in increasing Ce anomaly from the top of the profile downward.

Automated summary

The Huri bauxite deposit in northwestern Iran is found within carbonate footwalls of the Ruteh Formation. The bauxite ores consist of various minerals including hematite, diaspore, kaolinite, and traces of other minerals. Geochemical studies suggest that basalt rocks interbedded in limestone are the potential precursor rocks of the deposit, and various factors such as fluctuating groundwater table level and pH variations contributed to the mineral fractionation and anomalies.