Abstract

Crystallization temperatures of the 1.8 Ga Lofoten anorthosites are estimated from pyroxene thermometry, and pressure is derived from solving simultaneously the equilibria CaAl2SiO6(in cpx)+SiO2=CaAl2Si2O8(in plag)NaAlSi2O6(in cpx)+SiO2=NaAlSi3O8(in plag) and Mg2SiO4(in ol)+SiO2=2MgSiO3(in opx) These calculations indicate that the calcic Flakstadøy anorthosite [FBC, Cpx ± Ol ± Opx + Mtss + Ilmss + Plag (An57–47)] crystallized under polybaric conditions at pressures between 4 and 9 kbar and at temperatures between 1140 and 1185°C. The sodic Eidsfjord complex [Cpx + Opx + Mtss + Ilmss + Plag (An48–44)] crystallized at 1100–1135°C at a maximum pressure of 7.3 kbar. This technique may provide a means to estimate crystallization pressure and aSiO2 in many types of intrusive and extrusive rocks. Coeval mangerites and charnockites intruded subsequently at ∼4 kbar and temperatures between greater than 925°C and 800°C, respectively, indicated by the succession of the mafic phase assemblages (Cpx + Opx; Cpx + Opx + Ol; Cpx + Pig + Ol; Cpx + Ol) that reflect continuous fractionation to higher Fe/Mg ratios. The evidence for polybaric crystallization of the FBC quantitatively supports the common model that generation of Proterozoic anorthosites involves initial crystallization at depth (crust–mantle boundary) and intrusion as a crystal-rich mush. Detailed estimation of intrinsic parameters (P, T, fO2, aSiO2, fHCl) indicates a systematic relationship between the phase assemblages in anorthosites, ferrodiorites, mangerites and charnockites, which is compatible with fractional crystallization of a mafic parental magma.

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