Abstract
How eclogite/pyroxenite-derived melts evolve through the refractory lithosphere above a plume remains poorly understood. Here we conducted layered experiments of reaction between tholeiitic melts and harzburgite at 2–3 GPa, 1,400–1,500°C, with a run duration ranging from 2 to 24 hr. The resulting residual melts exhibit lower SiO2, TiO2, Al2O3, FeO, CaO, and total alkali contents, higher Ni, MgO, and Mg#, and almost constant CaO/Al2O3 compared to the initial tholeiitic melts. The compositions of the residual melts are influenced by factors such as the melt/harzburgite mass ratio, temperature, and run duration. Decreasing the melt/rock ratio or increasing temperature and run duration leads to a greater extent of assimilation. Under disequilibrated conditions (2 hr), the residual melts have higher SiO2, FeO, and MgO, and lower CaO, Al2O3, and total alkali contents compared to those under equilibrated conditions. The results suggest that interface reactions involving olivine dissolution and orthopyroxene precipitation, and chemical diffusion occur simultaneously during the interaction process. The compositions of the residual melts are largely controlled by interface reactions within 2 hr, followed by dominant chemical diffusion between the melts and refertilized harzburgite from 2 to 24 hr. Based on the experimental results, we propose a two-stage model for the origin of Hawaiian shield stage parental magmas. Eclogite/pyroxenite-derived tholeiitic melts first react with harzburgite, with varying melt/rock ratios, to produce residual melts in the deep lithosphere. These residual melts subsequently mix with plume peridotite-derived melts at shallow depths, contributing to the geochemical diversity observed in Hawaiian shield stage lavas.
