Carbon–oxygen isotope and trace element constraints on how fluids percolate faulted limestones from the San Andreas Fault system: partitioning of fluid sources and pathways

Abstract

Understanding the way fluids flow in fault zones is of prime importance to develop correct models of earthquake mechanics, especially in the case of the abnormally weak San Andreas Fault (SAF) system. Because fluid flow can leave detectable signatures in rocks, geochemistry is essential to bring light on this topic. The present detailed study combines, for the first time, C–O isotope analyses with a comprehensive trace element data set to examine the geometry of fluid flow within a significant fault system hosted by a carbonate sequence, from a single locality across the Little Pine Fault–SAF system. Such a fault zone contains veins, deformation zones, and their host rocks. Stable isotope geochemistry is used to establish a relative scale of integrated fluid–rock ratios. Carbonate δ 18O varies between 28‰ and 15‰ and δ 13C between 5‰ and −7‰. From highest to lowest delta values, thus from least to most infiltrated, are the host rocks, the vein fillings, and the deformation zone fillings, respectively. Infiltration increases toward fault core. The fluids are H 2O–CO 2 mixtures. Two fluid sources, one internal and the other external, are found. The external fluid is inferred to come essentially from metamorphism of the Franciscan formation underneath. The internal (local) fluid is provided by a 30% volume reduction of the host limestones resulting from pressure solution and pore size reduction. Most trace elements, including the lanthanides, show enrichment at the 100-m scale in host carbonate rocks as fluid–rock ratios increase toward the fault core. In contrast, the same trace element concentrations are low, relative to host rocks, in veins and deformation zone carbonate fillings, and this difference in concentration increases as fluid–rock ratio increases toward the fault core. We suggest that the fluid trace elements are scavenged by complexation with organic matter in the host rocks. Elemental complexation is especially illustrated by large fractionation of Y–Ho and Nb–Ta geochemical pairs. Complexation associated with external fluid flow has a significant effect on trace element enrichment (up to 700% relative enrichment) while concentration by pressure solution associated with volume decrease of host rocks has a more limited effect (up to 40% relative enrichment). Our observations from the millimeter to the kilometer scale call for the partitioning of fluid sources and pathways, and for a mixed focused–pervasive fluid flow mechanism. The fluid mainly flows within veins and deformation zones and, simultaneously, within at least 10 cm from these channels, part of the fluid flows pervasively in the host rock, which controls the fluid composition. Scavenging of the fluid rare earth elements (REE) by host rocks is responsible for the formation of REE-depleted vein and deformation zone carbonate fillings. Fluid flow is not only restricted to veins or deformation zones as commonly believed. An important part of fluid flow takes place in host rocks near fault zones. Hence, the nature of the lithologies hosting fault zones must be considered in order to take into account the role of fluids in the seismic cycle.