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Volume 14, issue 9
Atmos. Chem. Phys., 14, 4419–4439, 2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 14, 4419–4439, 2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 07 May 2014

Research article | 07 May 2014

The isotopic composition of water vapour and precipitation in Ivittuut, southern Greenland

J.-L. Bonne1, V. Masson-Delmotte1, O. Cattani1, M. Delmotte1, C. Risi3, H. Sodemann2, and H. C. Steen-Larsen1 J.-L. Bonne et al.
  • 1Laboratoire des Sciences du Climat et de l'Environnement, UMR8212, Gif sur Yvette, France
  • 2Institute for Atmospheric and Climate Science, ETH Zurich, Zurich, Switzerland
  • 3Laboratoire de Météorologie Dynamique, Paris, France

Abstract. Since September 2011, a wavelength-scanned cavity ring-down spectroscopy analyser has been remotely operated in Ivittuut, southern Greenland, providing the first record of surface water vapour isotopic composition based on continuous measurements in South Greenland and the first record including the winter season in Greenland. The comparison of vapour data with measurements of precipitation isotopic composition suggest an equilibrium between surface vapour and precipitation.

δ18O and deuterium excess are generally anti-correlated and show important seasonal variations, with respective amplitudes of ~10 and ~20‰, as well as large synoptic variations. The data depict small summer diurnal variations. At the seasonal scale, δ18O has a minimum in November–December and a maximum in June–July, while deuterium excess has a minimum in May–June and a maximum in November. The approach of low-pressure systems towards South Greenland leads to δ18O increase (typically +5‰) and deuterium excess decrease (typically −15‰).

Seasonal and synoptic variations coincide with shifts in the moisture sources, estimated using a quantitative moisture source diagnostic based on a Lagrangian back-trajectory model. The atmospheric general circulation model LMDZiso correctly captures the seasonal and synoptic variability of δ18O, but does not capture the observed magnitude of deuterium excess variability.

Covariations of water vapour isotopic composition with local and moisture source meteorological parameters have been evaluated. δ18O is strongly correlated with the logarithm of local surface humidity, consistent with Rayleigh distillation processes, and with local surface air temperature, associated with a slope of ~0.4‰ °C−1. Deuterium excess correlates with local surface relative humidity as well as surface relative humidity from the dominant moisture source area located in the North Atlantic, south of Greenland and Iceland.

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