Evolution of δ 56Fe in serpentinites during subduction: example in the Western Alps.
Abstract:
At mid-oceanic ridges, ultramafic rocks are serpentinized by interaction with seawater derived fluids. This process leads to the replacement and oxidation of ferromagnesian minerals (olivine and orthopyroxene) to Fe3+-rich lizardite and magnetite (Liz-serpentinite). Mantle peridotites commonly display δ56Fe between -0.1 and +0.1 ‰ while Liz-serpentinites display a δ56Fe ranging from -0.09 to +0.04 (± 0.03)‰, which could potentially reflect interactions with low-δ56Fe hydrothermal fluids. During subduction, from greenschist to blueschist facies, the transition lizardite to antigorite leads to a progressive disappearance of magnetite and a reduction of Fe in serpentine. This redox reaction is accompanied with an increase of δ56Fe from +0.03 to +0.13‰. At eclogite facies, fully recrystallized Atg-serpentinites display a δ56Fe ranging from +0.14 to +0.20‰ while partly dehydrated serpentinites composed of antigorite, secondary olivine and chlorite display a lower δ56Fe ranging from -0.03 to +0.03‰.
Our results show that, during the first 70 km of subduction, the transition lizardite to antigorite conduct to the formation of a serpentinite with a high δ56Fe value that can be accompanied with the loss of a low δ56Fe fluid. The increase of δ56Fe in serpentinites is correlated with a decrease of Fe3+/FeTot ratio suggesting that the main factor controlling Fe isotopic fractionation during the transition lizardite to antigorite is the oxidation state. At greater depth, antigorite breakdown is accompanied with a reduction of iron in serpentinites and a decrease of δ56Fe suggesting that release fluids could have a high δ56Fe value.
