scholarly journals Executive Editor Comment on "The TOMCAT global chemical transport model: Description of chemical mechanism and model evaluation"

2016 ◽  
Author(s):  
Astrid Kerkweg
2009 ◽  
Vol 2 (1) ◽  
pp. 185-207 ◽  
Author(s):  
P. Eller ◽  
K. Singh ◽  
A. Sandu ◽  
K. Bowman ◽  
D. K. Henze ◽  
...  

Abstract. This paper discusses the implementation and performance of an array of gas-phase chemistry solvers for the state-of-the-science GEOS-Chem global chemical transport model. The implementation is based on the Kinetic PreProcessor (KPP). Two perl parsers automatically generate the needed interfaces between GEOS-Chem and KPP, and allow access to the chemical simulation code without any additional programming effort. This work illustrates the potential of KPP to positively impact global chemical transport modeling by providing additional functionality as follows. (1) The user can select a highly efficient numerical integration method from an array of solvers available in the KPP library. (2) KPP offers extreme flexibility for studies that involve changing the chemical mechanism (e.g., a set of additional reactions is automatically translated into efficient code and incorporated into a modified global model). (3) This work provides immediate access to tangent linear, continuous adjoint, and discrete adjoint chemical models, with applications to sensitivity analysis and data assimilation.


2016 ◽  
Author(s):  
Sarah A. Monks ◽  
Stephen R. Arnold ◽  
Michael J. Hollaway ◽  
Richard J. Pope ◽  
Chris Wilson ◽  
...  

Abstract. The TOMCAT 3-D chemical transport model has been updated with the emissions and chemical degradation of ethene, propene, toluene, butane and monoterpenes. The full tropospheric chemical mechanism is described and the model is evaluated against a range of surface, balloon, aircraft and satellite measurements. The model is generally able to capture the main spatial and seasonal features of high and low concentrations of carbon monoxide (CO), ozone (O3), volatile organic compounds (VOCs) and reactive nitrogen. However, model biases are found, some of which are common to chemistry models and some that are specific to TOMCAT and warrant further investigation. Simulated O3 is found to generally lie within the range of ozonesonde observations and shows good agreement with surface sites. The most notable exceptions to this are during winter at high latitudes, when O3 is underestimated, and during summer over North America, when O3 is overestimated. Global Ozone Monitoring Experiment-2 (GOME-2) comparisons suggest that TOMCAT sub-column tropospheric O3 in DJF may also be underestimated outside of the Arctic, particularly near tropical regions. TOMCAT CO is negatively biased during winter and spring in the Northern Hemisphere (NH) when compared to ground-based observations and MOPITT (Measurements Of Pollution In The Troposphere) satellite data. In contrast, CO is positively biased throughout the year in the Southern Hemisphere (SH). The negative bias in the NH is a common feature in chemistry models and TOMCAT lies well within the range of biases found in other models, while the TOMCAT SH positive bias is at the upper range of positive biases reported in other models. Using two simulations with different boundary conditions highlighted the sensitivity of model performance to the chosen emission dataset when simulating VOCs, nitrogen oxides (NOx) and peroxyacetyl nitrate (PAN). VOC measurements show winter/spring negative biases in C2-C3 alkanes and alkenes, which is likely driven by underestimated anthropogenic emissions. TOMCAT is able to capture the seasonal minima and maxima of PAN and HNO3. However, comparisons to an aircraft climatology show that PAN may be overestimated in winter and HNO3 may be overestimated in winter and spring in regions over North America. The model showed different biases in NOx, depending on location, with evidence of underestimated Asian emissions contributing to negative model biases over China and underestimated fire emissions contributing to negative biases in the SH. TOMCAT global mean tropospheric hydroxyl radical (OH) concentrations are higher than estimates inferred from observations of methyl chloroform, but similar to, or lower than, multi-model mean concentrations reported in recent model intercomparison studies. TOMCAT shows peak OH concentrations in the tropical lower troposphere, unlike other models, which show peak concentrations in the tropical upper troposphere. This is likely to affect the lifetime and transport of important trace gases and warrants further investigation.


2009 ◽  
Vol 2 (2) ◽  
pp. 89-96 ◽  
Author(s):  
P. Eller ◽  
K. Singh ◽  
A. Sandu ◽  
K. Bowman ◽  
D. K. Henze ◽  
...  

Abstract. This paper discusses the implementation and performance of an array of gas-phase chemistry solvers for the state-of-the-science GEOS-Chem global chemical transport model. The implementation is based on the Kinetic PreProcessor (KPP). Two perl parsers automatically generate the needed interfaces between GEOS-Chem and KPP, and allow access to the chemical simulation code without any additional programming effort. This work illustrates the potential of KPP to positively impact global chemical transport modeling by providing additional functionality as follows. (1) The user can select a highly efficient numerical integration method from an array of solvers available in the KPP library. (2) KPP offers a wide variety of user options for studies that involve changing the chemical mechanism (e.g., a set of additional reactions is automatically translated into efficient code and incorporated into a modified global model). (3) This work provides access to tangent linear, continuous adjoint, and discrete adjoint chemical models, with applications to sensitivity analysis and data assimilation.


1998 ◽  
Vol 103 (D21) ◽  
pp. 28265-28289 ◽  
Author(s):  
G. P. Brasseur ◽  
D. A. Hauglustaine ◽  
S. Walters ◽  
P. J. Rasch ◽  
J.-F. Müller ◽  
...  

1999 ◽  
Vol 104 (D9) ◽  
pp. 11755-11781 ◽  
Author(s):  
Eugene V. Rozanov ◽  
Vladimir A. Zubov ◽  
Michael E. Schlesinger ◽  
Fanglin Yang ◽  
Natalia G. Andronova

2012 ◽  
Vol 5 (6) ◽  
pp. 1531-1542 ◽  
Author(s):  
L. K. Emmons ◽  
P. G. Hess ◽  
J.-F. Lamarque ◽  
G. G. Pfister

Abstract. A procedure for tagging ozone produced from NO sources through updates to an existing chemical mechanism is described, and results from its implementation in the Model for Ozone and Related chemical Tracers (MOZART-4), a global chemical transport model, are presented. Artificial tracers are added to the mechanism, thus, not affecting the standard chemistry. The results are linear in the troposphere, i.e., the sum of ozone from individual tagged sources equals the ozone from all sources to within 3% in zonal mean monthly averages. In addition, the tagged ozone is shown to equal the standard ozone, when all tropospheric sources are tagged and stratospheric input is turned off. The stratospheric ozone contribution to the troposphere determined from the difference between total ozone and ozone from all tagged sources is significantly less than estimates using a traditional stratospheric ozone tracer (8 vs. 20 ppbv at the surface). The commonly used technique of perturbing NO emissions by 20% in a region to determine its ozone contribution is compared to the tagging technique, showing that the tagged ozone is 2–4 times the ozone contribution that was deduced from perturbing emissions. The ozone tagging described here is useful for identifying source contributions based on NO emissions in a given state of the atmosphere, such as for quantifying the ozone budget.


Sign in / Sign up

Export Citation Format

Share Document