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Atmospheric modelling activities inside the Danish AMAP program

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Title: Atmospheric modelling activities inside the Danish AMAP program


1
Atmospheric modelling activities inside the
Danish AMAP program
  • Jesper H. Christensen
  • NERI-ATMI, Frederiksborgvej 399
  • 4000 Roskilde

2
The Danish Eulerian Hemispheric Model (DEHM)
System
  • The model work is financially supported by the
    Danish Environmental Protection Agency with means
    from the MIKA/DANCEA funds for Environmental
    Support to the Arctic Region
  • It is a part of the Danish contribution to the
    international AMAP programme
  • Purpose Study the long-range transport in the
    troposphere of pollutants into the Arctic
  • Developed since 1990. In the beginning only for
    Sulphur, later Lead and now also with a full
    photochemical scheme and Mercury.

3
The Danish Eulerian Hemispheric Model in 1. Phase
of AMAP
  • Direct coupling to ECMWF data, no MM5
    meteorological preprocessor
  • Simplified linear sulphur chemistry

4
The Danish Eulerian Hemispheric Model (DEHM)
System
5
MM5 model
  • Hydrostatisk version (version 2)
  • 150 km resolution at 60 N, 50 km for nested
    domain
  • 97x97 horizontal grid-points (for mother domain
    and 100x100 horizontal gridpoints for nested
    domain) and 20 vertical layers
  • Mixed Phase (Reisner) explicit moisture
  • Betts-Miller cumulus parametrization
  • MRF boundary layer parametrization with 5 layer
    soil model
  • Cloud-radiation scheme

6
  • Input data
  • Met data from ECMWF, 2.5x2.5 lat-lon,
  • 12 hour resolution, 21 years data from
    1979 to 2000
  • Output every 3 hours
  • Only run for 1990 to 2000 for hemispheric domain
    and
  • for 1995 and 1998 to 2000 for Europe (50 km)
  • 1 month for Greenland (50 km) as demonstration

7
The Danish Eulerian Hemispheric Model
  • Full three dimensional advection-diffusion
    equations
  • 150 km grid resolution (Mother domain)
  • 20 vertical levels up to 16 km
  • Dry deposition based on the resistance method
    with 8 different surfaces
  • Wet deposition based on scavenging coefficients
  • Numerical methods
  • Horizontal advection Accurate Space Derivatives
    with non-periodic boundary conditions and 2-way
    nesting capabilities
  • Vertical advection Finite Elements
  • Diffusion Finite Elements

8
Nested version of DEHMa demonstration with the
simplified sulphur version
150 km resolution
50 km resolution
9
The monthly mean concentrations for SOX
150 km resolution
50 km resolution
10
Mercury version of DEHM
  • Mercury model with GKSS chemistry
  • Gas phase pollutants Hg0 , HgO, HgCl2 and
    particulate Hg
  • 9 aqueous phase pollutants
  • Chemistry depending on O3, SO2, Cl- and Soot
  • During the polar sunrise in the Arctic an
    additional fast oxidation rate of Hg0 to HgO is
    assumed

From Petersen et al. (1998)
Wet removal rates for all aqueous phase
pollutants as for Sulphate Dry deposition velo
city for HgO and HgCl2 as for HNO3 and for
particulate Hg as for Sulphate
11
Examples of results with mercury model
12
Photochemical version of DEHM
  • Pollutants 54 species, more than 110 chemical
    reactions, chemistry scheme similar to the EMEP
    oxidant model
  • Emissions Global GEIA emissions of anthropogenic
    emissions of SOX and NOX, NOX from lightning and
    soil and Isoprene form vegetation, all on 1x 1
  • global EDGAR inventory on 1x 1 for
    anthropogenic hydrocarbons
  • SOX and NOX for Europe from EMEP
  • Has been run for whole 1998

13
Purpose with the photochemical version
  • Improvement of the parameterization of the
    chemistry compared to the simple sulfur model
  • Provided necessary input concentrations for the
    Mercury model
  • Be a useful contribution for the understanding of
    the atmospheric chemistry in the Arctic,
    especially during the Polar Sunrise in connection
    with field measurements
  • Provided necessary hemispheric background
    concentrations for the regional models, e.g. for
    Europe

14
Results from chemical version
NO2 mean concentrations
15
Ozone mean concentrations
16
Example of ozone transport into theNorth
Atlantic
17
Some validations
18
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19
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20
Ozone in the Arctic
21
Ongoing activities and future work
  • Continuing the work with parameterization of
    background chemistry, coupling with aqueous
    chemistry
  • Nested model calculations for Europe
  • Improve parameterization of Arctic chemistry,
    coupling with GOME measurement of BrO, coupled to
    measurements in the Arctic in order to understand
    the spatial and temporal distribution of the
    depletion


From Richter et al. (1997)
22
ACKNOWLEDGEMENTS
  • The model work is financially supported by the
    Danish Environmental Protection Agency with means
    from the MIKA/DANCEA funds for Environmental
    Support to the Arctic Region
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