MOZART, A GLOBAL CHEMICAL-TRANSPORT MODEL FOR OZONE AND RELATED CHEMICAL TRACERS 2 - MODEL RESULTS AND EVALUATION

Citation
Da. Hauglustaine et al., MOZART, A GLOBAL CHEMICAL-TRANSPORT MODEL FOR OZONE AND RELATED CHEMICAL TRACERS 2 - MODEL RESULTS AND EVALUATION, J GEO RES-A, 103(D21), 1998, pp. 28291-28335
Citations number
103
Categorie Soggetti
Metereology & Atmospheric Sciences","Geosciences, Interdisciplinary","Astronomy & Astrophysics",Oceanografhy,"Geochemitry & Geophysics
Volume
103
Issue
D21
Year of publication
1998
Pages
28291 - 28335
Database
ISI
SICI code
Abstract
In this second of two companion papers, we present results from a new global three-dimensional chemical transport model, called MOZART (mode l for ozone and related chemical tracers). MOZART is developed in the framework of the National Center for Atmospheric Research (NCAR) Commu nity Climate Model (CCM) and includes a detailed representation of tro pospheric chemistry. The model provides the distribution of 56 chemica l species at a spatial resolution of 2.8 degrees in both latitude and longitude, with 25 levels in the vertical (from the surface to level o f 3 mbar) and a time step of 20 min. The meteorological information is supplied from a 2-year run of the NCAR Community Climate Model. The s imulated distributions of ozone (O-3) and its precursors are evaluated by comparison with observational data. The distribution of methane, n onmethane hydrocarbons (NMHCs), and CO are generally well simulated by the model. The model evaluation in the tropics stresses the need for a better representation of biomass burning emissions in order to evalu ate the budget of carbon monoxide, nitrogen species, and ozone with mo re accuracy in these regions. MOZART reproduces the NO observations in most parts of the troposphere. Nitric acid, however, is overestimated over the Pacific by up to a factor of 10 and over continental regions by a factor of 2-3. Discrepancies are also found in the simulation of PAN in the upper troposphere and in biomass burning regions. These re sults highlight shortcomings in our understanding of the nitrogen budg et in the troposphere. The seasonal cycle of ozone in the troposphere is generally well reproduced by the model in comparison with ozone sou ndings. MOZART tends, however, to underestimate O-3 at higher latitude s, and specifically above 300 mbar. The global photochemical productio n and destruction of ozone in the troposphere are 3018 Tg/yr and 2511 Tg/yr, respectively (net ozone production of 507 Tg/yr). The stratosph eric influx of O-3 is estimated to be 391 Tg/yr and the surface dry de position 898 Tg/yr. The calculated global lifetime of methane is 9.9 y ears in the annual average.