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Atmospheric Measurement Techniques An interactive open-access journal of the European Geosciences Union
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Discussion papers
https://doi.org/10.5194/amt-2019-451
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/amt-2019-451
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.

Submitted as: research article 05 Dec 2019

Submitted as: research article | 05 Dec 2019

Review status
This discussion paper is a preprint. It is a manuscript under review for the journal Atmospheric Measurement Techniques (AMT).

N2O isotopocule measurements using laser spectroscopy: analyzer characterization and intercomparison

Stephen J. Harris1,2,*, Jesper Liisberg3,*, Longlong Xia4, Jing Wei5, Kerstin Zeyer5, Longfei Yu5, Matti Barthel6, Benjamin Wolf4, Bryce F. J. Kelly1, Dioni I. Cendón2, Thomas Blunier3, Johan Six6, and Joachim Mohn5 Stephen J. Harris et al.
  • 1School of Biological, Earth and Environmental Sciences, UNSW Sydney, NSW, Australia
  • 2Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW, Australia
  • 3University of Copenhagen, Niels Bohr Institute, Copenhagen, Denmark
  • 4Karlsruhe Institute of Technology, IMK-IFU, Garmisch-Partenkirchen, Germany
  • 5Empa, Laboratory for Air Pollution/Environmental Technology, Dübendorf, Switzerland
  • 6ETH Zürich, Department of Environmental Systems Science, Zürich, Switzerland
  • *These authors contributed equally to this work.

Abstract. For the past two decades, the measurement of N2O isotopocules – isotopically substituted molecules 14N15N16O, 15N14N16O and 14N14N18O of the main isotopic species 14N14N16O – has been a promising technique for understanding N2O production and consumption pathways. The coupling of non-cryogenic and tuneable light sources with different detection schemes, such as direct absorption quantum cascade laser absorption spectroscopy (QCLAS), cavity ring-down spectroscopy (CRDS) and off-axis integrated cavity output spectroscopy (OA-ICOS), has enabled the production of commercially-available and field-deployable N2O isotopic analyzers. In contrast to traditional isotope-ratio mass-spectrometry (IRMS), these instruments are inherently selective for position-specific 15N substitution and provide real-time data, with minimal or no sample pretreatment, which is highly attractive for process studies.

Here, we compared the performance of N2O isotope laser spectrometers with the three most common detection schemes: OA-ICOS (N2OIA-30e-EP, ABB-Los Gatos Research Inc.), CRDS (G5131-i, Picarro Inc.) and QCLAS (dual QCLAS and preconcentration (TREX)–mini QCLAS, Aerodyne Research Inc.). For each instrument, the precision, drift and repeatability of N2O mole fraction [N2O] and isotope data were tested. The analyzers were then characterized for their dependence on [N2O], gas matrix composition (O2, Ar) and spectral interferences caused by H2O, CO2, CH4 and CO to develop analyzer-specific correction functions. Subsequently, a simulated two end-member mixing experiment was used to compare the accuracy and repeatability of corrected and calibrated isotope measurements that could be acquired using the different laser spectrometers.

Our results show that N2O isotope laser spectrometer performance is governed by an interplay between instrumental precision, drift, matrix effects and spectral interferences. To retrieve compatible and accurate results, it is necessary to include appropriate reference materials following the identical treatment (IT) principle during every measurement. Remaining differences between sample and reference gas compositions have to be corrected by applying analyzer-specific correction algorithms. These matrix and trace gas correction equations vary considerably according to N2O mole fraction, complicating the procedure further. Thus, researchers should strive to minimize differences in composition between sample and reference gases. In closing, we provide a calibration workflow to guide researchers in the operation of N2O isotope laser spectrometers in order to acquire accurate N2O isotope analyses. We anticipate that this workflow will assist in applications where matrix and trace gas compositions vary considerably (e.g. laboratory incubations, N2O liberated from wastewater or groundwater), as well as extending to future analyzer models and instruments focusing on isotopic species of other molecules.

Stephen J. Harris et al.
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Short summary
The latest commercial laser spectrometers have the potential to revolutionize N2O isotope analysis. However, to do so, they must be able to produce trustworthy data. Here, we test the performance of widely used laser spectrometers for ambient air applications, and identify instrument-specific dependencies on gas matrix and trace gas concentrations. We then provide a calibration workflow to facilitate the operation of these instruments in order to generate reproducible and accurate data.
The latest commercial laser spectrometers have the potential to revolutionize N2O isotope...
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