A11I-0182
Understanding N2O sources and sinks with laser based isotopic analysis

Monday, 14 December 2015
Poster Hall (Moscone South)
Joachim Mohn, Empa, Laboratory for Air Pollution / Environmental Technology, Dübendorf, Switzerland
Abstract:
Nitrous oxide (N2O) is a potent greenhouse gas and the strongest stratospheric ozone-destroying substance released in the 21st century. Main N2O emissions are linked to different microbial pathways, therefore sources are disperse and highly variable, complicating their interpretation. Isotopic measurements have great potential to distinguish between individual source and sink processes. Developments in laser spectroscopy allow both the intramolecular distribution of 15N substitutions (15N14N16O versus 14N15N16O) and the oxygen isotopic composition of N2O to be measured in real-time, at high precision and in excellent compatibility to IRMS [1].

In a number of laboratory and pilot plant studies we investigated the isotopic signature of distinct microbial and abiotic N2O production and consumption pathways in soil and aqueous solution [e.g. 2-4]. Specific pathways were favoured by selection of the nitrogen substrates and process conditions and their isotopic signatures identified by real-time laser spectroscopic analysis. Results from our laboratory studies are in accordance with pure culture experiments and can therefore be applied to other ecosystems.

High precision isotopic analysis at ambient N2O concentration is feasible by combining laser spectroscopy with automated preconcentration. Field deployment was demonstrated by real-time monitoring of the isotopic composition of N2O emissions above an intensively managed grassland in central Switzerland. The responses of the N2O isotopic signatures were analysed with respect to management events and climatic conditions [5]. In a follow-up project we combine real-time N2O isotopic analysis at a tall tower in central Switzerland with atmospheric transport simulations and a biogeochemical model of surface fluxes of N2O isotopomers. The working hypothesis is that this approach will allow us to quantify regional N2O sources, identify emission hot spots, and constrain source processes, which will significantly advance our understanding of this important greenhouse gas.

[1] J. Mohn et al. Rapid Commun. Mass Spectrom. (2014) 28, 1995.
[2] J. Heil et al. Geochim. Cosmochim. Acta (2014) 139, 72
[3] P. Wunderlin et al. Environ. Sci. Technol. (2013) 47, 1339.
[4] E. Harris et al. Water Res. (2015) 83, 258.
[5] B. Wolf et al. Biogeosci. (2015) 12, 2517.