Matthias Sprenger

Illuminating hydrological processes at the soil‐vegetation‐atmosphere interface with water stable isotopes

Funded by DFG research project “From Catchments as Organised Systems to Models based on Functional Units” (FOR 1

Travel times in the vadose zone: Variability in space and time

Water travel times reflect hydrological processes, yet we know little about how travel times in the unsaturated zone vary with time. Using the soil physical model HYDRUS-1D, we derived time variable travel time distributions for 35 study sites within the Attert catchment in Luxembourg. While all sites experience similar climatic forcing, they differ with regard to soil types (16 Cambisols, 12 Arenosols, and 7 Stagnosols) and the vegetation cover (29 forest and 6 grassland). We estimated site specific water flow and transport parameters by fitting the model simulations to observed soil moisture time series and depth profiles of pore water stable isotopes. With the calibrated model, we tracked the water parcels introduced with each rainfall event over a period of several years. Our results show that the median travel time of water from the soil surface to depths down to 200 cm is mainly driven by the subsequent rainfall amounts. The median time until precipitation is taken up by roots is governed by the seasonality of evapotranspiration rates. The ratio between the amount of water that leaves the soil profile by on the one hand and evaporation and transpiration on the other hand also shows an annual cycle. This time variable response due to climatic forcing is furthermore visible in the multimodal nature of the site specific master transit time distribution representing the flow-averaged probability density for rainwater to become recharge. The spatial variability of travel times is mainly driven by soil texture and structure, with significant longer travel times for the clayey Stagnosols than for the loamy to sandy Cambisols and Arenosols.

Evaporation fractionation in a peatland drainage network affects stream water isotope composition

There is increasing interest in improving understanding of evaporation within a catchment for an enhanced representation of dominant processes in hydrological models. We used a dual‐isotope approach within a nested experimental design in a boreal catchment in the Scottish Highlands (Bruntland Burn) to quantify the spatiotemporal dynamics of evaporation fractionation in a peatland drainage network and its effect on stream water isotopes. We conducted spatially distributed water sampling within the saturated peatland under different wetness conditions. We used the lc‐excess—which describes the offset of a water sample from the local meteoric water line in the dual‐isotope space—to understand the development of kinetic fractionation during runoff in a peatland network. The evaporation fractionation signal correlated positively with the potential evapotranspiration and negatively with the discharge. The variability of the isotopic enrichment within the peatland drainage network was higher with higher potential evapotranspiration and lower with higher discharge. We found an increased evaporation fractionation toward the center of the peatland, while groundwater seepage from minerogenic soils influenced the isotopic signal at the edge of the peatland. The evaporation signal was imprinted on the stream water, as the discharge from a peatland dominated subcatchment showed a more intense deviation from the local meteoric water line than the discharge from the Bruntland Burn. The findings underline that evaporation fractionation within peatland drainage networks affects the isotopic signal of headwater catchments, which questions the common assumption in hydrological modeling that the isotopic composition of stream waters did not undergo fractionation processes.

Influence of forest and shrub canopies on precipitation partitioning and isotopic signatures

Over a four-month summer period, we monitored how forest (Pinus sylvestris) and heather moorland (Calluna spp. and Erica spp.) vegetation canopies altered the volume and isotopic composition of net precipitation (NP) in a southern boreal landscape in northern Scotland. During that summer period, interception (I) losses were relatively high, and higher under forests compared to moorland (46% of gross rainfall (GR) compared with 35%, respectively). Throughfall (TF) volumes exhibited marked spatial variability in forests, depending upon local canopy density, but were more evenly distributed under heather moorland. In the forest stands, stemflow (StF) was a relatively small canopy flow path accounting for only 0.9-1.6% of NP and only substantial in larger events. Overall, the isotopic composition of NP was not markedly affected by canopy interactions; temporal variation of stable water isotopes in TF closely corresponded to that of GR with differences of TF-GR being -0.52 ‰ for δ2H and -0.14 ‰ for δ18O for forests and 0.29 ‰ for δ2H and -0.04 ‰ for δ18O for heather moorland. These differences were close to, or within, analytical precision of isotope determination, though the greater differences under forest were statistically significant. Evidence for evaporative fractionation was generally restricted to low rainfall volumes in low intensity events, though at times subtle effects of liquid-vapour moisture exchange and/or selective transmission though canopies were evident. Fractionation and other effects were more evident in StF but only marked in smaller events. The study confirmed earlier work that increased forest cover in the Scottish Highlands will likely cause an increase in interception and green water fluxes at the expenses of blue water fluxes to streams. However, the low energy, humid environment means that isotopic changes during such interactions will only have a minor overall effect on the isotopic composition of NP.

No influence of CO2 on stable isotope analyses of soil waters with OA‐ICOS

Rationale It was recently shown that the presence of CO2 affects the stable isotope (δ2H and δ18O values) analysis of water vapor via Wavelength‐Scanned Cavity Ring‐Down Spectroscopy. Here, we test how much CO2 is emitted from soil samples and if the CO2 in the headspace influences the isotope analysis with the direct equilibration method by Off‐Axis Integrated Cavity Output Spectroscopy (OA‐ICOS). Methods The headspace above different amounts of sparkling water was sampled, and its stable isotopic composition (δ2H and δ18O values) and CO2 concentration were measured by direct equilibration and by gas chromatography, respectively. In addition, the headspace above soil samples was analyzed in the same way. Furthermore, the gravimetric water content and the loss on ignition were measured for the soil samples. Results The experiment with the sparkling water showed that CO2 does not influence the stable isotope analysis by OA‐ICOS. CO2 was emitted from the soil samples and correlated with the isotopic fractionation signal, but no causal relationship between the two was determined. Instead, the fractionation signal in pore water isotopes can be explained by soil evaporation and the CO2 can be related to soil moisture and organic matter which both enhance microbial activity. Conclusions We found, despite the high CO2 emissions from soil samples, no need for a post‐correction of the pore water stable isotope analysis results, since there is no relation between CO2 concentrations and the stable isotope results of vapor samples obtained with OA‐ICOS.

Storage, mixing and fluxes of water in the critical zone across northern environments inferred by stable isotopes of soil water

We thank Audrey Innes for isotope analysis at University of Aberdeen for Bruntland Burn and Krycklan sites, Johannes Tiwari (SLU) for isotope sampling in Krycklan, Pernilla Lofvenius (SLU) for providing PET data for Krycklan (via SITES), and Jeff McDonnell and Kim Janzen (University of Saskatchewan) for soil water isotope analysis for the Dorset and Wolf Creek sites. The Krycklan part was funded by the KAW Branch-Point project. We acknowledge the funding from the European Research Council (ERC, project GA 335910 VeWa). We thank the Editor and three anonymous reviewers for their critical comments during the peer-review process.

No influence of CO2 on stable isotope analyses of soil waters with off-axis integrated cavity output spectroscopy (OA-ICOS).

Rationale It was recently shown that the presence of CO2 affects the stable isotope (δ2H and δ18O values) analysis of water vapor via Wavelength‐Scanned Cavity Ring‐Down Spectroscopy. Here, we test how much CO2 is emitted from soil samples and if the CO2 in the headspace influences the isotope analysis with the direct equilibration method by Off‐Axis Integrated Cavity Output Spectroscopy (OA‐ICOS). Methods The headspace above different amounts of sparkling water was sampled, and its stable isotopic composition (δ2H and δ18O values) and CO2 concentration were measured by direct equilibration and by gas chromatography, respectively. In addition, the headspace above soil samples was analyzed in the same way. Furthermore, the gravimetric water content and the loss on ignition were measured for the soil samples. Results The experiment with the sparkling water showed that CO2 does not influence the stable isotope analysis by OA‐ICOS. CO2 was emitted from the soil samples and correlated with the isotopic fractionation signal, but no causal relationship between the two was determined. Instead, the fractionation signal in pore water isotopes can be explained by soil evaporation and the CO2 can be related to soil moisture and organic matter which both enhance microbial activity. Conclusions We found, despite the high CO2 emissions from soil samples, no need for a post‐correction of the pore water stable isotope analysis results, since there is no relation between CO2 concentrations and the stable isotope results of vapor samples obtained with OA‐ICOS.

No influence of CO2on stable isotope analyses of soil waters with off-axis integrated cavity output spectroscopy (OA-ICOS): CO2effects for direct equilibration

Rationale It was recently shown that the presence of CO2 affects the stable isotope (δ2H and δ18O values) analysis of water vapor via Wavelength‐Scanned Cavity Ring‐Down Spectroscopy. Here, we test how much CO2 is emitted from soil samples and if the CO2 in the headspace influences the isotope analysis with the direct equilibration method by Off‐Axis Integrated Cavity Output Spectroscopy (OA‐ICOS). Methods The headspace above different amounts of sparkling water was sampled, and its stable isotopic composition (δ2H and δ18O values) and CO2 concentration were measured by direct equilibration and by gas chromatography, respectively. In addition, the headspace above soil samples was analyzed in the same way. Furthermore, the gravimetric water content and the loss on ignition were measured for the soil samples. Results The experiment with the sparkling water showed that CO2 does not influence the stable isotope analysis by OA‐ICOS. CO2 was emitted from the soil samples and correlated with the isotopic fractionation signal, but no causal relationship between the two was determined. Instead, the fractionation signal in pore water isotopes can be explained by soil evaporation and the CO2 can be related to soil moisture and organic matter which both enhance microbial activity. Conclusions We found, despite the high CO2 emissions from soil samples, no need for a post‐correction of the pore water stable isotope analysis results, since there is no relation between CO2 concentrations and the stable isotope results of vapor samples obtained with OA‐ICOS.