ChemInform Abstract: Carbonyl Oxides-Rising Stars in Tropospheric Chemistry

ChemInform ◽  
2014 ◽  
Vol 45 (19) ◽  
pp. no-no
Author(s):  
Wolfram Sander
2001 ◽  
Vol 32 ◽  
pp. 269-270
Author(s):  
J.E. WILLIAMS ◽  
F.J. DENTENER ◽  
A.R. van den BERG

2019 ◽  
Vol 12 (9) ◽  
pp. 3863-3887 ◽  
Author(s):  
Aryeh Feinberg ◽  
Timofei Sukhodolov ◽  
Bei-Ping Luo ◽  
Eugene Rozanov ◽  
Lenny H. E. Winkel ◽  
...  

Abstract. SOCOL-AERv1 was developed as an aerosol–chemistry–climate model to study the stratospheric sulfur cycle and its influence on climate and the ozone layer. It includes a sectional aerosol model that tracks the sulfate particle size distribution in 40 size bins, between 0.39 nm and 3.2 µm. Sheng et al. (2015) showed that SOCOL-AERv1 successfully matched observable quantities related to stratospheric aerosol. In the meantime, SOCOL-AER has undergone significant improvements and more observational datasets have become available. In producing SOCOL-AERv2 we have implemented several updates to the model: adding interactive deposition schemes, improving the sulfate mass and particle number conservation, and expanding the tropospheric chemistry scheme. We compare the two versions of the model with background stratospheric sulfate aerosol observations, stratospheric aerosol evolution after Pinatubo, and ground-based sulfur deposition networks. SOCOL-AERv2 shows similar levels of agreement as SOCOL-AERv1 with satellite-measured extinctions and in situ optical particle counter (OPC) balloon flights. The volcanically quiescent total stratospheric aerosol burden simulated in SOCOL-AERv2 has increased from 109 Gg of sulfur (S) to 160 Gg S, matching the newly available satellite estimate of 165 Gg S. However, SOCOL-AERv2 simulates too high cross-tropopause transport of tropospheric SO2 and/or sulfate aerosol, leading to an overestimation of lower stratospheric aerosol. Due to the current lack of upper tropospheric SO2 measurements and the neglect of organic aerosol in the model, the lower stratospheric bias of SOCOL-AERv2 was not further improved. Model performance under volcanically perturbed conditions has also undergone some changes, resulting in a slightly shorter volcanic aerosol lifetime after the Pinatubo eruption. With the improved deposition schemes of SOCOL-AERv2, simulated sulfur wet deposition fluxes are within a factor of 2 of measured deposition fluxes at 78 % of the measurement stations globally, an agreement which is on par with previous model intercomparison studies. Because of these improvements, SOCOL-AERv2 will be better suited to studying changes in atmospheric sulfur deposition due to variations in climate and emissions.


1989 ◽  
Vol 54 (7) ◽  
pp. 1612-1616 ◽  
Author(s):  
J. C. Scaiano ◽  
W. G. McGimpsey ◽  
H. L. Casal

1996 ◽  
Vol 252 (3-4) ◽  
pp. 221-229 ◽  
Author(s):  
Roland Gutbrod ◽  
Ralph N. Schindler ◽  
Elfi Kraka ◽  
Dieter Cremer

2016 ◽  
Vol 9 (9) ◽  
pp. 3071-3091 ◽  
Author(s):  
Vincent Huijnen ◽  
Johannes Flemming ◽  
Simon Chabrillat ◽  
Quentin Errera ◽  
Yves Christophe ◽  
...  

Abstract. We present a model description and benchmark evaluation of an extension of the tropospheric chemistry module in the Integrated Forecasting System (IFS) of the European Centre for Medium-Range Weather Forecasts (ECMWF) with stratospheric chemistry, referred to as C-IFS-CB05-BASCOE (for brevity here referred to as C-IFS-TS). The stratospheric chemistry originates from the one used in the Belgian Assimilation System for Chemical ObsErvations (BASCOE), and is here combined with the modified CB05 chemistry module for the troposphere as currently used operationally in the Copernicus Atmosphere Monitoring Service (CAMS). In our approach either the tropospheric or stratospheric chemistry module is applied, depending on the altitude of each individual grid box with respect to the tropopause. An evaluation of a 2.5-year long C-IFS-TS simulation with respect to various satellite retrieval products and in situ observations indicates good performance of the system in terms of stratospheric ozone, and a general improvement in terms of stratospheric composition compared to the C-IFS predecessor model version. Possible issues with transport processes in the stratosphere are identified. This marks a key step towards a chemistry module within IFS that encompasses both tropospheric and stratospheric composition, and could expand the CAMS analysis and forecast capabilities in the near future.


1996 ◽  
Vol 14 (6) ◽  
pp. 659-664 ◽  
Author(s):  
A. V. Ivanov ◽  
Y. M. Gershenzon ◽  
F. Gratpanche ◽  
P. Devolder ◽  
J.-P. Sawerysyn

Abstract. The uptake coefficients (Γ) for OH radicals on some dry salts of tropospheric interest (NaCl and NH4NO3) have been investigated as a function of temperature using the flow tube technique combined with an EPR spectrometer as a detection method. The temperature dependence of Γ-values measured over the temperature range 245–340 K can be expressed in Arrhenius form: ΓOHNaCl=(1.2±0.7)×10–5exp[(1750±200)/T] and ΓOHNH4NO3=(1.4±0.5)×10–4exp[(1000±100)/T]. These Arrhenius expressions lead to very similar Γ-values (~4×10–3) for both salts studied at 300 K. It is shown that the heterogeneous OH sinks on solids aerosol play a very minor role in tropospheric chemistry in comparison with the homogeneous sinks.


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