Technical note : Conservative storage of water vapour - practical in situ sampling of stable isotopes in tree stems

Publisher Copyright: © Copyright:Using water-stable isotopes to track plant water uptake or soil water processes has become an invaluable tool in ecohydrology and physiological ecology. Recent studies have shown that laser absorption spectroscopy can measure equilibrated water vapour well enough to support inference of liquid-stable isotope composition of plant or soil water, on-site and in real-Time. However, current in situ systems require the presence of an instrument in the field. Here we tested, first in the lab and then in the field, a method for equilibrating, collecting, storing, and finally analysing water vapour for its isotopic composition that does not require an instrument in the field. We developed a vapour storage vial system (VSVS) that relies on in situ sampling into crimp neck vials with a double-coated cap using a pump and a flow metre powered through a small battery and measuring the samples in a laboratory. All components are inexpensive and commercially available. We tested the system's ability to store the isotopic composition of its contents by sampling a range of water vapour of known isotopic compositions (from-95g to +1700g for 2H) and measuring the isotopic composition after different storage periods. Samples for the field trial were taken in a boreal forest in northern Sweden. The isotopic composition was maintained to within 0.6g to 4.4g for 2H and 0.6g to 0.8g for 18O for natural-Abundance samples. Although 2H-enriched samples showed greater uncertainty, they were sufficient to quantify label amounts. We detected a small change in the isotopic composition of the sample after a long storage period, but it was correctable by linear regression models. We observed the same trend for the samples obtained in the field trial for 18O but observed higher variation in 2H than in the lab trial. Our method combines the best of two worlds, sampling many trees in situ while measuring at high precision in the laboratory. This provides the ecohydrology community with a tool that is not only cost efficient but also easy to use.Peer reviewe

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

Acknowledgements We are thankful for the support by Audrey Innes with the stable isotope, LOI, and GWC analysis. We thank Jonathan Dick for suggesting that we use sparkling water to generate different CO2 concentrations in the headspace and Claire Tunaley for proof reading. We further highly appreciate the help of David Galloway and Michael Mcgibbon from the School of Biological Sciences, University of Aberdeen, with the CO2 analysis. We are also thankful for the support by Robert Provencal and Doug S. Baer regarding the technical aspects of the isotope analyzer. We would also like to thank the European Research Council (ERC, Project No. GA 335910 VeWa) and the Natural Environment Research Council (NERC, Project No. NE/K000268/1) for funding. We thank three anonymous reviewers for their valuable feedback that helped to improve the manuscript.Peer reviewedPublisher PD

Technical note : Conservative storage of water vapour - practical in situ sampling of stable isotopes in tree stems

Publisher Copyright: © Copyright:Using water-stable isotopes to track plant water uptake or soil water processes has become an invaluable tool in ecohydrology and physiological ecology. Recent studies have shown that laser absorption spectroscopy can measure equilibrated water vapour well enough to support inference of liquid-stable isotope composition of plant or soil water, on-site and in real-time. However, current in situ systems require the presence of an instrument in the field. Here we tested, first in the lab and then in the field, a method for equilibrating, collecting, storing, and finally analysing water vapour for its isotopic composition that does not require an instrument in the field. We developed a vapour storage vial system (VSVS) that relies on in situ sampling into crimp neck vials with a double-coated cap using a pump and a flow metre powered through a small battery and measuring the samples in a laboratory. All components are inexpensive and commercially available. We tested the system's ability to store the isotopic composition of its contents by sampling a range of water vapour of known isotopic compositions (from -95 parts per thousand to +1700 parts per thousand for delta H-2) and measuring the isotopic composition after different storage periods. Samples for the field trial were taken in a boreal forest in northern Sweden. The isotopic composition was maintained to within 0.6 parts per thousand to 4.4 parts per thousand for delta H-2 and 0.6 parts per thousand to 0.8 parts per thousand for delta O-18 for natural-abundance samples. Although H-2-enriched samples showed greater uncertainty, they were sufficient to quantify label amounts. We detected a small change in the isotopic composition of the sample after a long storage period, but it was correctable by linear regression models. We observed the same trend for the samples obtained in the field trial for delta O-18 but observed higher variation in delta H-2 than in the lab trial. Our method combines the best of two worlds, sampling many trees in situ while measuring at high precision in the laboratory. This provides the ecohydrology community with a tool that is not only cost efficient but also easy to use.Peer reviewe

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 1Peer reviewedPublisher PDFPublisher PD

Inter-laboratory comparison of cryogenic water extraction systems for stable isotope analysis of soil water

For more than two decades, research groups in hydrology, ecology, soil science, and biogeochemistry have performed cryogenic water extractions (CWEs) for the analysis of δ2H and δ18O of soil water. Recent studies have shown that extraction conditions (time, temperature, and vacuum) along with physicochemical soil properties may affect extracted soil water isotope composition. Here we present results from the first worldwide round robin laboratory intercomparison. We test the null hypothesis that, with identical soils, standards, extraction protocols, and isotope analyses, cryogenic extractions across all laboratories are identical. Two standard soils with different physicochemical characteristics along with deionized (DI) reference water of known isotopic composition were shipped to 16 participating laboratories. Participants oven-dried and rewetted the soils to 8 and 20 % gravimetric water content (WC), using the deionized reference water. One batch of soil samples was extracted via predefined extraction conditions (time, temperature, and vacuum) identical to all laboratories; the second batch was extracted via conditions considered routine in the respective laboratory. All extracted water samples were analyzed for δ18O and δ2H by the lead laboratory (Global Institute for Water Security, GIWS, Saskatoon, Canada) using both a laser and an isotope ratio mass spectrometer (OA-ICOS and IRMS, respectively). We rejected the null hypothesis. Our results showed large differences in retrieved isotopic signatures among participating laboratories linked to soil type and soil water content with mean differences compared to the reference water ranging from +18.1 to −108.4 ‰ for δ2H and +11.8 to −14.9 ‰ for δ18O across all laboratories. In addition, differences were observed between OA-ICOS and IRMS isotope data. These were related to spectral interferences during OA-ICOS analysis that are especially problematic for the clayey loam soils used. While the types of cryogenic extraction lab construction varied from manifold systems to single chambers, no clear trends between system construction, applied extraction conditions, and extraction results were found. Rather, observed differences in the isotope data were influenced by interactions between multiple factors (soil type and properties, soil water content, system setup, extraction efficiency, extraction system leaks, and each lab's internal accuracy). Our results question the usefulness of cryogenic extraction as a standard for water extraction since results are not comparable across laboratories. This suggests that defining any sort of standard extraction procedure applicable across laboratories is challenging. Laboratories might have to establish calibration functions for their specific extraction system for each natural soil type, individually.</p

Forum Übergang - Lehrer/innen und Erzieher/innen gestalten gemeinsam einen kindgerechten Übergang von der Kita in die Grundschule

In der Maria-Montessori-Grundschule in Berlin-Tempelhof findet ein bis zweimal im Halbjahr am späten Nachmittag ein Treffen von Pädagog/innen statt. Es handelt sich nicht um eine Lehrerkonferenz. Es ist ein freiwilliges Treffen von Pädagog/innen der Grundschule und der Kitas in ihrem Einzugsgebiet, ein Forum des Austauschs und der Arbeit an pädagogischen Themen, die sowohl Kita-Erzieher/innen als auch Lehrer/innen in der Schulanfangsphase betreffen. In den Sitzungen behandeln die Mitglieder des Forums wechselnde pädagogische Schwerpunkte, d. h. verschiedene Inhalte, die das Thema des Übergangs der Kinder aus der Kita in die Grundschule betreffen. (Autor

Correcting for biogenic gas matrix effects on laser-based pore water-vapor stable isotope measurements.

The isotopic composition (δ2H, δ18O) of pore water is an invaluable tracer for the minimally invasive study of subsurface water flow and transport processes. Here, we evaluated a method for pore water isotope analysis that combines laser-based isotope analyzers and water-vapor isotope equilibration using evaporation- proof metalized sample bags. We tested inflation atmospheres (dry air vs. pure N2) and the impact of biogenic gas (CO2, CH4) accumulation for storage times of up to 4 wk. Samples were analyzed with a water isotope analyzer (Picarro L2120-i) and a gas chromatograph. Air-inflated water vapor samples showed a greater range of gas matrix effects (δ18O: 9.63‰; δ2H: 21.7‰) than N2–inflated samples (δ18O: 7.49‰; δ2H: 10.6‰) induced by nonuniform buildup of biogenic CO2, starting immediately after sample preparation. However, only air-inflated samples could be reliably corrected using instrument-specific sensitivity factors that were empirically determined by interpretation of periodically repeated isotope measurements. Corrected water isotope data were confirmed by similarity with local precipitation and suction cup isotope data. Residual uncertainties were well below the natural variations of soil water isotope values and independent of storage time, thus allowing for consistently reliable interpretations of soil water isotope profiles. We conclude that, especially for pore water sampling that requires small sample volumes and/or long storage times, metalized sample bags should be used to prevent evaporation notwithstanding the enhanced buildup of biogenic gases. Further, if gas matrix effects cannot be excluded, air inflation is preferred over pure N2, as only in that case can reliable postcorrections be performed by using internal data only