Abstract:
We have investigated the stability and composition of potassium amphibole and its high-pressure breakdown product phase X in synthetic peralkaline and subalkaline KNCMASH (K 2 O–Na 2 O–CaO–MgO–Al 2 O 3 –SiO 2 –H 2 O) and natural KLB-1 peridotite bulk compositions between 10 and 23 GPa at 800–1800°C. In the KNCMASH system, potassium amphibole reaches its upper pressure stability limit at 13–15 GPa at ≤1400°C. In the natural KLB-1 bulk composition, potassium amphibole breaks down between 12 and 13 GPa at 1200°C. Phase X is a hydrous potassium–magnesium silicate with variable stoichiometry, a general formula K 2–x Mg 2 Si 2 O 7 H x with x = 0–1, and a maximum possible H 2 O content of 3·5 wt %. Electron microprobe analytical totals suggest H 2 O contents of ∼1–2 wt % and a decrease in H 2 O contents with increasing pressure. In both KNCMASH and KLB-1 systems, phase X coexists with Mg 2 SiO 4 + garnet + high-Ca clinopyroxene + low-Ca clinopyroxene ± fluid. Phase X breaks down between 20 and 23 GPa at 1500–1700°C to form K-hollandite + γ-Mg 2 SiO 4 + majorite + Ca-perovskite + fluid. The upper temperature stability limit of phase X was located in the subalkaline KNCMASH system between 1400 and 1600°C at 14 GPa and at >1700°C at 20 GPa, the latter being at least 200°C above an average current mantle adiabat. Thus, phase X could store and transport both water and potassium not only in subduction zone settings, but also in convecting mantle down to the transition zone–lower-mantle boundary. Phase X would also be an eminently suitable host for Rb, Cs, Ba or Pb.
