Rare earth elements (REEs) play a critical role in provenance tracing and the environmental reconstruction of the Earth. However, systematic investigations into the geochemical behavior and fractionation mechanisms of REEs during halite crystallization in brine–salt systems remain limited. This study reports new trace element and REE data for Late Cretaceous halites from the Thakhek Basin, Laos. Ratios of Sr/Ba, Sr/Cu, and V/Cr indicate a marine origin for the halites, which formed under hot climatic and oscillating oxidizing–anoxic redox conditions. Both primary and secondary halites display uniform Post-Archean Australian Shale (PAAS)-normalized REE distribution patterns, characterized by relative enrichment in medium rare earth elements (MREE) and depletion in light (LREE) and heavy rare earth elements (HREE). Similar REE patterns are also observed in halites from other modern and ancient, continental and marine salt basins worldwide. These observations suggest that the influences of parent brine composition and external provenance supplies on REE fractionation are negligible, given the consistent source, salinity, and redox conditions recorded in these halites. Accordingly, REE fractionation in halite was largely controlled by crystallographic effects, with aqueous MREE preferentially incorporated into halite crystals during deposition. In addition, the relatively lower Zr/Hf ratios in secondary halites compared to primary halites further validate the utility of the Zr/Hf ratio for distinguishing authigenic halite from salt modified by diagenesis, weathering, dissolution, or recrystallization. While our results establish a fundamental REE distribution pattern for halite, further research is needed to better constrain the underlying fractionation mechanisms of REEs in evaporite minerals within brine–salt systems.
Sha et al. (Thu,) studied this question.