ISOTOPIC AND ELEMENTAL ZONING IN GARNET REVEALS MULTIPLE MECHANISMS OF CHEMICAL TRANSFER IN SUBDUCTION ZONES (Invited Presentation)
Along core–rim transects, small-wavelength (< 300 µm-wide) vacillations in elemental and oxygen isotopic composition are superimposed on grain-scale elemental zonation. Across garnet rims, little to no net variation in δ18O is typically observed. However, garnets from Oman display a distinct break between a low-Al, high-Eu core and high-Al, low-Eu mantle–rim zone, and δ18O values that decrease continuously (rimward) across the mantle–rim zone of the garnets. This grain-scale zonation is interpreted to record large-scale influx of reducing, low-δ18O fluids.
Small wavelength elemental vacillations most clearly observed in Mn are axisymmetric for a given garnet and comparable among garnets at the rock scale. Conversely, small wavelength δ18O vacillations are not axisymmetric nor comparable among garnets from a single thin section. Principle component analyses suggest no covariance among the short-wavelength elemental and δ18O zoning patterns, meaning they likely have independent origins. The δ18O vacillations may record disconnected, isotopically distinct pore fluid reservoirs resulting from heterogeneous dehydration processes. The elemental vacillations may be explained by pulses of rock-wide element supply and/or solubility increase that coincide with high grain boundary permeability. The data from this study support a view of chemical transfer in subduction zones that involves: (1) long-distance, transient and channelized fluid transfer events not ‘seen’ by most rocks in the subduction zone; (2) an ambient state of highly disconnected grain boundary porosity; and (3) episodic, rock-scale high grain boundary permeability events that may involve P and/or T spikes. Seismic events may play a significant role in enabling periodic rock-scale chemical transfer/equilibration.