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  Reconstruction of Northern Hemisphere 1950-2010 atmospheric non-methane hydrocarbons

Helmig, D., Petrenko, V., Martinerie, P., Witrant, E., Röckmann, T., Zuiderweg, A., et al. (2014). Reconstruction of Northern Hemisphere 1950-2010 atmospheric non-methane hydrocarbons. Atmospheric Chemistry and Physics, 14(3), 1463-1483. doi:10.5194/acp-14-1463-2014.

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Helmig, D.1, Author
Petrenko, V.1, Author
Martinerie, P.1, Author
Witrant, E.1, Author
Röckmann, T.1, Author
Zuiderweg, A.1, Author
Holzinger, R.1, Author
Hueber, J.1, Author
Thompson, C.1, Author
White, J. W. C.1, Author
Sturges, W.1, Author
Baker, A.2, Author           
Blunier, T.1, Author
Etheridge, D.1, Author
Rubino, M.1, Author
Tans, P.1, Author
Affiliations:
1external, ou_persistent22              
2Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826285              

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 Abstract: The short-chain non-methane hydrocarbons (NMHC) are mostly emitted into the atmosphere by anthropogenic processes. Recent studies have pointed out a tight linkage between the atmospheric mole fractions of the NMHC ethane and the atmospheric growth rate of methane. Consequently, atmospheric NMHC are valuable indicators for tracking changes in anthropogenic emissions, photochemical ozone production, and greenhouse gases. This study investigates the 1950-2010 Northern Hemisphere atmospheric C-2-C-5 NMHC ethane, propane, i-butane, n-butane, i-pentane, and n-pentane by (a) reconstructing atmospheric mole fractions of these trace gases using firn air extracted from three boreholes in 2008 and 2009 at the North Greenland Eemian Ice Drilling (NEEM) site and applying state-of-the-art models of trace gas transport in firn, and by (b) considering eight years of ambient NMHC monitoring data from five Arctic sites within the NOAA Global Monitoring Division (GMD) Cooperative Air Sampling Network. Results indicate that these NMHC increased by similar to 40-120% after 1950, peaked around 1980 (with the exception of ethane, which peaked approximately 10 yr earlier), and have since dramatically decreased to be now back close to 1950 levels. The earlier peak time of ethane vs. the C-3-C-5 NMHC suggests that different processes and emissions mitigation measures contributed to the decline in these NMHC. The 60 yr record also illustrates notable increases in the ratios of the isomeric iso-/n-butane and iso-/n-pentane ratios. Comparison of the reconstructed NMHC histories with 19502000 volatile organic compounds (VOC) emissions data and with other recently published ethane trend analyses from ambient air Pacific transect data showed (a) better agreement with North America and Western Europe emissions than with total Northern Hemisphere emissions data, and (b) better agreement with other Greenland firn air data NMHC history reconstructions than with the Pacific region trends. These analyses emphasize that for NMHC, having atmospheric lifetimes on the order of <2 months, the Greenland firn air records are primarily a representation of Western Europe and North America emission histories.

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 Dates: 2014
 Publication Status: Issued
 Pages: -
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 Rev. Type: -
 Identifiers: ISI: 000332384900020
DOI: 10.5194/acp-14-1463-2014
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Title: Atmospheric Chemistry and Physics
Source Genre: Journal
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Publ. Info: Katlenburg-Lindau, Germany : European Geosciences Union
Pages: - Volume / Issue: 14 (3) Sequence Number: - Start / End Page: 1463 - 1483 Identifier: ISSN: 1680-7316
CoNE: https://pure.mpg.de/cone/journals/resource/111030403014016