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Verification of German methane emission inventories and their recent changes based on atmospheric observations
Author(s) -
Levin Ingeborg,
GlatzelMattheier Holger,
Marik Thomas,
Cuntz Matthias,
Schmidt Martina,
Worthy Douglas E.
Publication year - 1999
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/1998jd100064
Subject(s) - methane , environmental science , atmospheric sciences , flux (metallurgy) , trace gas , mixing ratio , tracer , atmospheric methane , soil water , hydrology (agriculture) , geology , chemistry , soil science , physics , organic chemistry , geotechnical engineering , nuclear physics
Continuous methane concentration records and stable isotope observations measured in the suburbs of Heidelberg, Germany, are presented. While δ 13 C‐CH 4 shows a significant trend of −0.14‰ per year, toward more depleted values, no trend is observed in the concentration data. Comparison of the Heidelberg records with clean air observations in the North Atlantic at Izaña station (Tenerife) allows the determination of the continental methane excess at Heidelberg, decreasing by 20% from 190 ppb in 1992 to 150 ppb in 1997. The isotope ratio which is associated with this continental methane pileup in the Heidelberg catchment area shows a significant trend to more depleted values from δ 13 C source = −47.4 ± 1.2‰ in 1992 to −52.9 ± 0.4‰ in 1995/1996, pointing to a significant change in the methane source mix. Total methane emissions in the Heidelberg catchment area are estimated using the 222 radon ( 222 Rn) tracer method: from the correlations of half‐hourly 222 Rn and CH 4 mixing ratios from 1995 to 1997, and the mean 222 Rn exhalation rate from typical soils in the Rhine valley, a mean methane flux of 0.24 ± 0.5 g CH 4 km −2 s −1 is derived. For the Heidelberg catchment area with an estimated radius of approximately 150 km, Core Inventories Air 1990 (CORINAIR90) emission estimates yield a flux of 0.47 g CH 4 km −2 s −1 , which is about 40% higher than the 222 Rn‐derived number if extrapolated to 1990. The discrepancy can be explained by overestimated emissions from waste management in the CORINAIR90 statistical assessment. The observed decrease in total emissions can be accounted for by decreasing contributions from fossil sources (mainly coal mining) and from cattle breeding. This finding is also supported by the observed decrease in mean source isotopic signatures.

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