Reconstructing the lithium isotope composition (δ7Li) of ancient seawater and lacustrine environment is crucial for tracing silicate weathering processes that regulate Earth's carbon cycle and climate. This study examines the reliability of evaporite minerals in preserving the Li isotope signature of the original brines from which they precipitate. We conducted evaporation experiments on modern natural waters from Qinghai Lake, the Yellow Sea, and Chaka Salt Lake, each with unique salinity and chemical composition, to examine the behavior of lithium isotope ratios in the evolving brine and precipitated evaporite minerals.Our results show that initial hydrochemical conditions of the lake and ocean are the primary control on the evolution of major and trace elements and the mineral precipitation sequences during evaporative concentration. Aragonite, calcite, gypsum, and/or nesquehonite precipitated prior to halite. Li isotope fractionation of these non-halite precipitates varied significantly between 4‰ and 17‰. However, the δ7Li values of halite closely mirror those of the initial lake and seawater, indicating negligible Li isotope fractionation (<1‰) during halite precipitation. The δ7Li values of the evolving brines remain unchanged throughout the evaporation experiment. Solid phases precipitating before halite constitute <1–2% of the total moles of salt precipitated from the complete evaporation of the initial waters, thus, having little to no influence on the δ7Li values of evolving brines. Although halite comprises >77% of the total moles of salt, it does not fractionate Li isotopes. Therefore, halite more accurately reflects the δ7Li values of the co-evolving brine as well as those of the initial, unevaporated lake and seawater. These results underscore the potential of late stage evaporites, particularly halite, to serve as high-fidelity archives of ancient lacustrine and seawater δ7Li values. Such records are instrumental in reconstructing past silicate weathering and climatic conditions.