Marc Ulrich

Syn-tectonic, meteoric water-derived carbonation of the New Caledonia peridotite nappe

Exceptional outcrops recently exposed in the Koniambo massif allow the study of the serpentine sole of the peridotite nappe of New Caledonia (southwest Pacific Ocean). Many magnesite veins are observed, with characteristics indicating that they were emplaced during pervasive top-to-the-southwest shear deformation. The oxygen isotope composition of magnesite is homogeneous (27.4‰ < δ18O < 29.7‰), while its carbon isotope composition varies widely (−16.7‰ < δ13C < −8.5‰). These new data document an origin of magnesite from meteoric fluids. Laterization on top of the peridotite nappe and carbonation along the sole appear to represent complementary records of meteoric water infiltration. Based on the syn-kinematic character of magnesite veins, we propose that syn-laterization tectonic activity has enhanced water infiltration, favoring the exportation of leached elements like Mg, which has led to widespread carbonation along the serpentine sole. This calls for renewed examination of other magnesite-bearing ophiolites worldwide in order to establish whether active tectonics is commonly a major agent for carbonation.

Dissolution–precipitation processes governing the carbonation and silicification of the serpentinite sole of the New Caledonia ophiolite

Abstract The weathering of mantle peridotite tectonically exposed to the atmosphere leads commonly to natural carbonation processes. Extensive cryptocrystalline magnesite veins and stock-work are widespread in the serpentinite sole of the New Caledonia ophiolite. Silica is systematically associated with magnesite. It is commonly admitted that Mg and Si are released during the laterization of overlying peridotites. Thus, the occurrence of these veins is generally attributed to a per descensum mechanism that involves the infiltration of meteoric waters enriched in dissolved atmospheric CO2. In this study, we investigate serpentinite carbonation processes, and related silicification, based on a detailed petrographic and crystal chemical study of serpentinites. The relationships between serpentine and alteration products are described using an original method for the analysis of micro-X-ray fluorescence images performed at the centimeter scale. Our investigations highlight a carbonation mechanism, together with precipitation of amorphous silica and sepiolite, based on a dissolution–precipitation process. In contrast with the per descensum Mg/Si-enrichment model that is mainly concentrated in rock fractures, dissolution–precipitation process is much more pervasive. Thus, although the texture of rocks remains relatively preserved, this process extends more widely into the rock and may represent a major part of total carbonation of the ophiolite.