Atmospheric Acetylene and its Relationship with CO as an Indicator of Air Mass Age

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Atmospheric Acetylene and its Relationship with CO as an Indicator of Air Mass Age

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dc.contributor.author Xiao, Yaping
dc.contributor.author Jacob, Daniel J.
dc.contributor.author Turquety, Solene
dc.date.accessioned 2011-02-14T14:53:16Z
dc.date.issued 2007
dc.identifier.citation Xiao, Yaping, Daniel J. Jacob, and Solene Turquety. 2007. Atmospheric acetylene and its relationship with CO as an indicator of air mass age. Journal of Geophysical Research 112: D12305. en_US
dc.identifier.issn 0148-0227 en_US
dc.identifier.uri http://nrs.harvard.edu/urn-3:HUL.InstRepos:4724834
dc.description.abstract Acetylene (C2H2) and CO originating from combustion are strongly correlated in atmospheric observations, offering constraints on atmospheric dilution and chemical aging. We examine here the C2H2-CO relationships in aircraft observations worldwide, and interpret them with simple models as well as with a global chemical transport model (GEOS-Chem). A C2H2 global source of 6.6 Tg yr−1 in GEOS-Chem simulates the ensemble of global C2H2 observations without systematic bias, and captures most seasonal and regional features. C2H2/CO concentration ratios decrease from continental source regions to the remote atmosphere in a manner consistent between the observations and the model. However, the dC2H2/dCO slope from the linear regression does not show such a systematic decrease, either in the model or in the observations, reflecting variability in background air. The slope β = dlog[C2H2]/dlog[CO] of the linear regression of concentrations in log space offers information for separating the influences of dilution and chemical aging. We find that a linear mixing model with constant dilution rate and background is successful in fresh continental outflow but not in remote air. A diffusion model provides a better conceptual framework for interpreting the observations, where the value of β relative to the square root of the ratio of C2H2 and CO chemical lifetimes (1.7–1.9) measures the relative importance of dilution and chemistry. We thus find that dilution dominates in fresh outflow but chemical loss dominates in remote air. This result is supported by GEOS-Chem sensitivity simulations with modified OH concentrations, and suggests that the model overestimates OH in the southern tropics. en_US
dc.description.sponsorship Earth and Planetary Sciences en_US
dc.description.sponsorship Engineering and Applied Sciences en_US
dc.language.iso en_US en_US
dc.publisher American Geophysical Union en_US
dc.relation.isversionof doi:10.1029/2006JD008268 en_US
dc.relation.hasversion http://acmg.seas.harvard.edu/cvdj.html en_US
dash.license META_ONLY
dc.title Atmospheric Acetylene and its Relationship with CO as an Indicator of Air Mass Age en_US
dc.type Journal Article en_US
dc.description.version Version of Record en_US
dc.relation.journal Journal of Geophysical Research -All Series- en_US
dash.depositing.author Jacob, Daniel J.
dash.embargo.until 10000-01-01

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  • FAS Scholarly Articles [7588]
    Peer reviewed scholarly articles from the Faculty of Arts and Sciences of Harvard University

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