Journal cover Journal topic
Biogeosciences An interactive open-access journal of the European Geosciences Union
Journal topic
Volume 12, issue 8
Biogeosciences, 12, 2517-2531, 2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.
Biogeosciences, 12, 2517-2531, 2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 29 Apr 2015

Research article | 29 Apr 2015

First on-line isotopic characterization of N2O above intensively managed grassland

B. Wolf1,2, L. Merbold3, C. Decock3, B. Tuzson1, E. Harris1, J. Six3, L. Emmenegger1, and J. Mohn1 B. Wolf et al.
  • 1Laboratory for Air Pollution/Environmental Technology, Empa, Überlandstrasse 129, 8600 Dübendorf, Switzerland
  • 2Institute for Meteorology and Climate Research (IMK-IFU), Karlsruhe Institute of Technology, Kreuzeckbahnstrasse 19, 82467 Garmisch-Partenkirchen, Germany
  • 3Department of Environmental Systems Science, ETH Zurich, Universitätsstrasse 2, 8092 Zürich, Switzerland

Abstract. The analysis of the four main isotopic N2O species (14N14N16O, 14N15N16O, 15N14N16O, 14N14N18O) and especially the intramolecular distribution of 15N ("site preference", SP) has been suggested as a tool to distinguish source processes and to help constrain the global N2O budget. However, current studies suffer from limited spatial and temporal resolution capabilities due to the combination of discrete flask sampling with subsequent laboratory-based mass-spectrometric analysis. Quantum cascade laser absorption spectroscopy (QCLAS) allows the selective high-precision analysis of N2O isotopic species at trace levels and is suitable for in situ measurements.

Here, we present results from the first field campaign, conducted on an intensively managed grassland site in central Switzerland. N2O mole fractions and isotopic composition were determined in the atmospheric surface layer (at 2.2 m height) at a high temporal resolution with a modified state-of-the-art laser spectrometer connected to an automated N2O preconcentration unit. The analytical performance was determined from repeated measurements of a compressed air tank and resulted in measurement repeatability of 0.20, 0.12 and 0.11‰ for δ15Nα, δ15Nβ and δ18O, respectively. Simultaneous eddy-covariance N2O flux measurements were used to determine the flux-averaged isotopic signature of soil-emitted N2O.

Our measurements indicate that, in general, nitrifier-denitrification and denitrification were the prevalent sources of N2O during the campaign and that variations in isotopic composition were due to alterations in the extent to which N2O was reduced to N2 rather than to other pathways, such as hydroxylamine oxidation. Management and rewetting events were characterized by low values of the intramolecular 15N site preference (SP), δ15Nbulk and δ18O, suggesting that nitrifier-denitrification and incomplete heterotrophic bacterial denitrification responded most strongly to the induced disturbances. The flux-averaged isotopic composition of N2O from intensively managed grassland was 6.9 ± 4.3, −17.4 ± 6.2 and 27.4 ± 3.6‰ for SP, δ15Nbulk and δ18O, respectively. The approach presented here is capable of providing long-term data sets also for other N2O-emitting ecosystems, which can be used to further constrain global N2O inventories.

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