Atmos. Chem. Phys., 16, 14891–14908, 2016 www.atmos-chem-phys.net/16/14891/2016/ doi:10.5194/acp-16-14891-2016 © Author(s) 2016. CC Attribution 3.0 License. 13 Using δ C-CH4 and δD-CH4 to constrain Arctic methane emissions Nicola J. Warwick1,2, Michelle L. Cain1, Rebecca Fisher3, James L. France4, David Lowry3, Sylvia E. Michel5, Euan G. Nisbet3, Bruce H. Vaughn5, James W. C. White5, and John A. Pyle1,2 1National Centre for Atmospheric Science, NCAS, UK 2Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK 3Department of Earth Sciences, Royal Holloway, University of London, Egham, TW20 0EX, UK 4School of Environmental Sciences, University of East Anglia, Norwich, NR4 7TJ, UK 5Institute of Arctic and Alpine Research (INSTAAR), University of Colorado, Boulder, CO 80309, USA Correspondence to: Nicola J. Warwick (
[email protected]) Received: 23 May 2016 – Published in Atmos. Chem. Phys. Discuss.: 28 June 2016 Revised: 21 October 2016 – Accepted: 27 October 2016 – Published: 1 December 2016 Abstract. We present a global methane modelling study 2007, the Arctic experienced a rapid methane increase, but assessing the sensitivity of Arctic atmospheric CH4 mole in 2008 and 2009–2010 growth was strongest in the trop- 13 fractions, δ C-CH4 and δD-CH4 to uncertainties in Arctic ics. This renewed global increase in atmospheric methane has methane sources. Model simulations include methane trac- been accompanied by a shift towards more 13C-depleted val- ers tagged by source and isotopic composition and are com- ues, suggesting that one explanation for the change could be pared with atmospheric data at four northern high-latitude an increase in 13C-depleted wetland emissions (Nisbet et al., measurement sites.