Biogeochemical processes in a clay formation in situ experiment: Part B – Results from overcoring and evidence of strong buffering by the rock formation
2011
Koroleva, M. | Lerouge, C. | Mäder, U. | Claret, F. | Gaucher, E.
An in situ Porewater Chemistry (PC) experiment in the Opalinus Clay formation was carried out at the Mont Terri underground rock laboratory (Jura Mountains, Switzerland) for a period of 5a. A traced water with a composition close to that expected in the formation was continuously circulated and monitored in a packed-off borehole to achieve diffusive equilibration. An unwanted microbial perturbation changed the water composition, characterized by reduction of SO₄ combined with increasing sulfide, increasing alkalinity, decreasing pH and increasing P(CO₂). In contrast, the main cations (Na, Ca, Mg) remained remarkably constant during the experiment, thus indicating the strong buffering of the formation via cation and proton exchange as well as carbonate dissolution/precipitation reactions. After 5a, the 4.5m long vertical test interval was overcored and Opalinus Clay samples were analyzed along ca. 15cm long radial profiles. The analytical investigations included mineralogy (XRD, SEM-EDX), bulk parameters (water content, density, C, S), cation exchange capacity and occupancy, aqueous leachates for Cl⁻, Br⁻, SO₄ ²⁻ and water and carbonate stable isotopes. Emphasis was put on best sample preparation and conservation techniques. Results show that the distribution of non-reactive tracers (Br⁻ and ²H) follows the expected out/in-diffusion profiles compatible with the time-dependent boundary conditions in the test interval of the borehole. Although some experimental features remain unresolved (e.g. high content of leachable SO₄ ²⁻ compared to the test interval), the distribution of reactive tracers (in porewater, on the clay exchanger and in the solid phase) demonstrate the very extensive buffer capacity of the Opalinus Clay formation towards chemical disturbances, such as those induced by microbial SO₄ reduction and oxidation of an organic C source.
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