Long-term and high frequency non-destructive monitoring of water stable isotope profiles in an evaporating soil column
Abstract. The stable isotope compositions of soil water (δ2H and δ18O) carry important information about the prevailing soil hydrological conditions and for constraining ecosystem water budgets. However, they are highly dynamic, especially during and after precipitation events. The classical method of determining soil water δ2H and δ18O at different depths, i.e., soil sampling and cryogenic extraction of the soil water, followed by isotope-ratio mass spectrometer analysis is destructive and laborious with limited temporal resolution. In this study, we present a new non-destructive method based on gas-permeable tubing and isotope-specific infrared laser absorption spectroscopy. We conducted a laboratory experiment with an acrylic glass column filled with medium sand equipped with gas-permeable tubing at eight different soil depths. The soil column was initially saturated from the bottom, exposed to evaporation for a period of 290 days, and finally rewatered. Soil water vapor δ2H and δ18O were measured daily, sequentially for each depth. Soil liquid water δ2H and δ18O were inferred from the isotopic values of the vapor assuming thermodynamic equilibrium between liquid and vapor phases in the soil. The experimental setup allowed following the evolution of typical exponential-shaped soil water δ2H and δ18O profiles with unprecedentedly high temporal resolution. As the soil dried out, we could also show for the first time the increasing influence of the isotopically depleted ambient water vapor on the isotopically enriched liquid water close to the soil surface (i.e., atmospheric invasion). Rewatering at the end of the experiment led to instantaneous resetting of the stable isotope profiles, which could be closely followed with the new method.