Quantitative analysis of mass transfer during polymetamorphism in pelites of the Transangarian Yenisei Ridge

摘要

The study provides geological, structural, mineralogical, petrological, and geochronological evidence for polymetamorphic evolution of gneisses from the Garevka complex of the Yenisei Ridge. The results of the study provide significant insight into the geochemical behavior of major and trace elements in zoned garnet crystals and mineral inclusions formed during prograde and retrograde metamorphism of pelitic rocks. It was shown that the concentrations of Y and HREE in garnet decrease with increasing P and T and increase with decreasing pressure and temperature. The combined study of multicomponent chemical zoning patterns of coexisting minerals and metamorphic mineral reactions in metapelites was conducted. The results show that the main reason for a drastic increase in CaO content in garnets during collisional metamorphism is a mass exchange between garnet and plagioclase. The deviation from this trend, as indicated by the concurrent increase in the grossular content of garnet and anorthite content of plagioclase, arises from the breakdown of epidote. The calculated metamorphic reactions, mass balance analysis, and changes in mineral chemistry during metamorphism reinforce the evidence for the isochemical character of processes with respect to most components of the system. The minimum volume of the system in which chemical exchange between reacting phases is balanced for all major and trace elements did not exceed similar to 1 mm(3). The total HREE balance requires a greater reaction volume (up to similar to 8 mm(3)) involved in the redistribution of these elements, which provide evidence for their relatively higher mobility during metamorphism relative to other rare earth elements. The specific distribution and quite substantial mass transport of HREE are controlled by heterovalent isomorphic substitution between these elements and CaO in garnet. (C) 2016, V.S. Sobolev IGM, Siberian Branch of the RAS. Published by Elsevier B.V. All rights reserved.