The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
A two‐dimensional photochemical model of the atmosphere: 2. The tropospheric budgets of the anthropogenic chlorocarbons CO, CH4, CH3Cl and the effect of various NOx sources on tropospheric ozone
Abstract
This paper presents two‐dimensional photochemical model simulations that show the influence of the various NOx sources from industry, lightning, the stratosphere, and aircraft on the tropospheric distributions of NOx, HNO 3, and O 3. We found that, by far, the best agreement with the global observations is obtained if the industrial sources are included in the calculations. Industrial activities have led to substantial increases of ozone concentrations in the lower troposphere of the northern hemisphere. Emissions of NOx by high‐flying aircraft have only a small effect on ozone concentrations in the troposphere. The ability of the model to simulate the global distributions of the long‐lived chlorocarbons CFCl 3 and CF 2 Cl 2 indicates that the interhemispheric exchange is rather well described. The model confirms an earlier finding by Rowland et al. (1982) that the CF 2 Cl 2 emission rates estimated by the Chemical Manufacturers Association (CMA) may be 35–40% lower for the period 1976 through 1980. The model also supports the earlier finding of Hyson et al. (1980) that CFCl 3 is apparently increasing roughly 10% faster than the CMA emission rates can account for during the period 1976 through 1980. Although this disparity could be explained by assuming 10% higher emission rates for CFCl 3 during the period, the behavior of the interhemispheric gradient indicates that errors in the determination of the absolute concentrations could also be an explanation. The ability of the model to simultaneously simulate measured distributions of the shorter‐lived chlorocarbons CH 3 CCl 3, CH 2 Cl 2, C 2 HCl 3, and C 2 Cl 4 indicates that its average OH concentrations are also about correct. Based on these OH concentrations, the model tropospheric budgets of CO, CH 4, and CH 3 Cl are calculated. The computed losses of CO, CH 4, and CH 3 Cl by reaction with OH are 2.1×10 15 g CO yr−1, 3.2×10 14 g CH 4 yr−1, and 1.9× 0 12 g CH 3 Cl yr−1, respectively.
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Citations
Cites
Stratospheric sink for chlorofluoromethanes: chlorine atom-catalysed destruction of ozone
Molina, M. J., & Rowland, F. S. (1974) · Nature · doi:10.1038/249810a0 · Cited by 4,332
Microphysics of Clouds and Precipitation
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Tropospheric chemistry: A global perspective
Logan, J. A., Prather, M. J., Wofsy, S. C., & McElroy, M. B. (1981) · Journal of Geophysical Research: Oceans · doi:10.1029/jc086ic08p07210 · Cited by 1,888
Normal Atmosphere: Large Radical and Formaldehyde Concentrations Predicted
Levy, H. (1971) · Science · doi:10.1126/science.173.3992.141 · Cited by 1,076
The Role of NO and NO2 in the Chemistry of the Troposphere and Stratosphere
Crutzen, P. J. (1979) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev.ea.07.050179.002303 · Cited by 933
Self-citationStratospheric-Tropospheric Exchange Based on Radioactivity, Ozone and Potential Vorticity
Danielsen, E. F. (1968) · Journal of the Atmospheric Sciences · doi:10.1175/1520-0469(1968)025<0502:stebor>2.0.co;2 · Cited by 887
Biomass burning as a source of atmospheric gases CO, H2, N2O, NO, CH3Cl and COS
Crutzen, P. J., Heidt, L. E., Krasnec, J. P., Pollock, W. H., & Seiler, W. (1979) · Nature · doi:10.1038/282253a0 · Cited by 775
Self-citationByers, H. R., Landsberg, H. E., Wexler, H., Haurwitz, B., Spilhaus, A. F., Willett, H. C., & Houghton, H. G. (1951) · American Meteorological Society eBooks · doi:10.1007/978-1-940033-70-9 · Cited by 747
A discussion of the chemistry of some minor constituents in the stratosphere and troposphere
Crutzen, P. (1973) · Pure and Applied Geophysics · doi:10.1007/bf00881092 · Cited by 514
Self-citationA photochemical theory of tropospheric ozone
Chameides, W., & Walker, J. C. G. (1973) · Journal of Geophysical Research · doi:10.1029/jc078i036p08751 · Cited by 496
Cited by
Liu, S. C., Trainer, M., Fehsenfeld, F. C., Parrish, D. D., Williams, E. J., Fahey, D. W., Hübler, G., & Murphy, P. C. (1987) · Journal of Geophysical Research: Atmospheres · doi:10.1029/jd092id04p04191 · Cited by 990
Three‐dimensional climatological distribution of tropospheric OH: Update and evaluation
Spivakovsky, C. M., Logan, J. A., Montzka, S. A., Balkanski, Y. J., Foreman‐Fowler, M., Jones, D. B. A., Horowitz, L. W., Fusco, A. C., Brenninkmeijer, C. A. M., Prather, M. J., et al. (2000) · Journal of Geophysical Research: Atmospheres · doi:10.1029/1999jd901006 · Cited by 910
Can, M., Armstrong, F. A., & Ragsdale, S. W. (2014) · Chemical Reviews · doi:10.1021/cr400461p · Cited by 622
Future global warming from atmospheric trace gases
Dickinson, R. E., & Cicerone, R. J. (1986) · Nature · doi:10.1038/319109a0 · Cited by 600
Distribution, diversity and ecology of aerobic CO-oxidizing bacteria
King, G. M., & Weber, C. F. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1595 · Cited by 437
Metadata
- Authors
- Crutzen, P. J., & Gidel, L. T.
- Venue
- Journal of Geophysical Research: Oceans
- Publisher
- American Geophysical Union (AGU)
- Published
- 1983-08-20
- Volume
- 88
- Issue
- C11
- Pages
- 6641-6661
- ISSN
- 0148-0227 (ISSN-L)
- OpenAlex
- W2144583704
- Cited by
- 285
- References
- 58
- FWCI
- 21.32
- Type
- journal article
- Language
- en
- Open access
- closed
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- Crutzen, P. J., & Gidel, L. T. (1983). A two‐dimensional photochemical model of the atmosphere: 2. The tropospheric budgets of the anthropogenic chlorocarbons CO, CH4, CH3Cl and the effect of various NOx sources on tropospheric ozone. Journal of Geophysical Research: Oceans. https://doi.org/10.1029/jc088ic11p06641
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