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. In this study, we present an application of a method based on gas-permeable tubing and isotope-specific infrared laser absorption spectroscopy for in situ determination of soil water δ2H and δ18O. We conducted a laboratory experiment where a sand column was initially saturated, exposed to evaporation for a period of 290 days, and finally rewatered. Soil water vapor δ2H and δ18O were measured daily at each of eight available depths. Soil liquid water δ2H and δ18O were inferred from those of the vapor considering thermodynamic equilibrium between liquid and vapor phases in the soil. The experimental setup allowed for following the evolution of soil water δ2H and δ18O profiles with a daily temporal resolution. As the soil dried, 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. From simple soil δ2H and δ18O gradients calculations, we showed that the gathered data allowed one to determinate the depth of the evaporation front (EF) and how it receded into the soil over time. It was inferred that after 290 days under the prevailing experimental conditions, the EF had moved down to an approximate depth of −0.06 m. Finally, data were used to calculate the slopes of the evaporation lines and test the formulation for kinetic isotope effects. A very good agreement was found between measured and simulated values (Nash and Sutcliffe efficiency, NSE = 0.92) during the first half of the experiment, i.e., until the EF reached a depth of −0.04 m. From this point, calculated kinetic effects associated with the transport of isotopologues in the soil surface air layer above the EF provided slopes lower than observed. Finally, values of kinetic isotope effects that provided the best model-to-data fit (NSE > 0.9) were obtained from inverse modeling, highlighting uncertainties associated with the determinations of isotope kinetic fractionation and soil relative humidity at the EF.
The understanding of the dissolution and precipitation of minerals and its impact on the transport of fluids in porous media is essential for various subsurface applications, including shale gas production using hydraulic fracturing (“fracking”), CO2 sequestration, or geothermal energy extraction. In this work, we conducted a flow through column experiment to investigate the effect of barite precipitation following the dissolution of celestine and consequential permeability changes. These processes were assessed by a combination of 3D non-invasive magnetic resonance imaging, scanning electron microscopy, and conventional permeability measurements. The formation of barite overgrowths on the surface of celestine manifested in a reduced transverse relaxation time due to its higher magnetic susceptibility compared to the original celestine. Two empirical nuclear magnetic resonance (NMR) porosity–permeability relations could successfully predict the observed changes in permeability by the change in the transverse relaxation times and porosity. Based on the observation that the advancement of the reaction front follows the square root of time, and micro-continuum reactive transport modelling of the solid/fluid interface, it can be inferred that the mineral overgrowth is porous and allows the diffusion of solutes, thus affecting the mineral reactivity in the system. Our current investigation indicates that the porosity of the newly formed precipitate and consequently its diffusion properties depend on the supersaturation in solution that prevails during precipitation.
19 February 2019 in Journal of Experimental Botany
Functional–structural root-system models simulate the relations between root-system architectural and hydraulic properties, and the spatio-temporal distributions of water and solutes in the root zone. Such models may help identify optimal plant properties for breeding and contribute to increased water-use efficiency. However, it must first be demonstrated that they accurately reproduce the processes they intend to describe. This is challenging because the flow and transport processes towards individual roots are hard to observe. In this study, we demonstrate how this problem can be addressed by combining co-registered root and tracer distributions obtained from magnetic resonance imaging with a root-system model in an inverse modeling scheme. The main features in the tracer distributions were well reproduced by the model using realistic root hydraulic parameters. By combining the functional–structural root-system model with 4D tracer observations, we were able to quantify the water uptake distribution of a growing root system. We determined that 76% of the transpiration was extracted through 3rd-order roots. The simulations also demonstrated that accurate water uptake distribution cannot be directly derived either from observations of tracer accumulation or from water depletion. However, detailed tracer experiments combined with process-based models help decipher mechanisms underlying root water uptake.
Magnetic resonance imaging (MRI) was applied to the study of flow processes in model and natural soil cores. Flow velocities in soils are mostly too slow to be monitored directly by MRI flow velocity imaging. Therefore, we used for the first time diethylenetriaminepentaacetate in the form Gd‐DTPA 2− as a tracer in spin echo multislice imaging protocols with strong weighting of longitudinal relaxation time T1 for probing slow flow velocities in soils. Apart from its chemical stability, the main advantage of Gd‐DTPA 2− is the anionic net charge in neutral aqueous solution. We showed that this property hinders adsorption at soil mineral surfaces and therefore retardation. We found that Gd‐DTPA 2− is a very convenient conservative tracer for the investigation of flow processes in model and natural soil cores. With respect to the flow processes in the coaxial model soil column and the natural soil column, we observed totally different flow patterns. In the first case, the tracer plume moved quite homogeneously in the inner highly conductive core only and the migration into the outer fine material was very limited. A numerical forward simulation based on independently obtained parameters showed good agreement between experiment and simulation and thus proves the convenience of Gd‐DTPA as a tracer in MRI for soil physical investigations. The natural soil core, in contrast, showed a flow pattern characterized by preferential paths, avoiding dense regions and preferring loose structures. In the case of the simpler model column, the local flow velocities were also calculated by applying a peak tracking algorithm.