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1
monoxide (CO), nitrogen oxides (NOX), sulfur pollutant emissions (e.g., biogenic and mobile
dioxide (SO2), nonmethane volatile organic sources) depend on meteorology. In the second
compounds (NMVOC), ammonia (NH3), and case the combined impact of future emissions
speciated particulate matter (PM10 and PM2.5). A (based on the forecast emissions and climate) and
detailed description of the method has been future climate is evaluated to simulate future levels
presented by Woo et al., (2006). of O3 and PM2.5. Average regional concentrations
are predicted for five continental US sub-regions,
2.2 Meteorology West, Plains, Midwest, Northeast and Southeast
Meteorological fields are derived from the (Figure 1).
Goddard Institute of Space Studies (GISS) Global
Climate Model (GCM) (Rind et al., 1999), which
was applied at a horizontal resolution of 4o latitude 3. RESULTS AND DISCUSSION
by 5o longitude to simulate current and future
climate at global scale. The simulation followed 3.1 Emissions
the SRES-A1B emission scenario (IPCC, 2000) for Emissions changes between future (2050) and
greenhouse gases. Leung and Gustafson, (2005) historic (2001) years show large decreases in SO2
downscaled GISS outputs using the Penn (-50%) and NOx (-50%) when climate change,
State/NCAR Mesoscale Model (MM5) (Grell et al., growth in human activities and emission controls
1994) to the regional scale (Figure 1). The are simulated (Figure 2). These reductions are
Meteorology Chemistry Interface Processor due to control strategies applied to anthropogenic
(MCIP) (http://www.cmascenter.org) is used to US and Canadian sources while the growth of the
provide the meteorological data from the hourly industrial sector gives higher emissions in Mexico.
MM5 outputs needed for the emissions and air Emission reductions in anthropogenic VOC’s
quality models that both have 147x111 horizontal combined with the higher biogenic emissions in
grids of 36 km x 36 km, with nine (9) vertical layers the warmer climate results in a small change in
up to approximately 15 km. VOCs emissions (+2%). For the case where only
climatic changes are considered, VOC emissions
are slightly higher (+15%) in the future due to
temperature effect on biogenic and mobile
sources. Minor increases in NOX (+2%) and SO2
(+4%) are also predicted. Description of the
regional emissions is detailed in Woo et al.,
(2006).
2001
80
2050
2050_np
70
Emissions (million tons per year)
60
50
40
30
10
0
NOX VOC PM25 SO2 NH3
2.3 Air Quality Modeling
CMAQ (Byun, 1999) with SAPRC-99 (Carter,
2000) is used to simulate the historic (i.e. Figure 2: Annual emissions for 200, 2050 and
summers 2000 – 2002) and future (i.e. summers 2050 for the “no emissions projection” scenario
2049 - 2051) ozone and PM2.5 concentrations. For (2050_np)
the future period, two different cases are
examined. In the first case the same emission
state, i.e., the 2001 inventory, is used for both 3.2 Meteorology
historic and future simulations in order to estimate Future summer temperatures (i.e., 2049-2050)
the impact to air quality by changes in global compared to the historic ones (i.e., 2000-2002) are
climate alone. Although the emission inventory is simulated to be 1.4K warmer in US (Figure 3), with
kept the same, emissions are not, since some small variations by region (± 0.6K). The minimum
2
increase is noted in the Midwest (0.8K) and the 16
Summers 2000-2002
Summers 2049-2051
Summers 2000-2051_np
maximum in the West (2.0K). A detailed climate
14
12
PM2.5 (μg/m )
3
2045-2055 has been presented by Leung and 8
Gustafson (2005). 4
0
West Plains Midwest Northeast Southeast US
Summers 2000-2002
Regions
305 Summers 2049-2051
300
295
Figure 5: Mean summer PM2.5 concentrations for
historic and future periods
290
Temperature (K)
285
280
275
270
The impact of climate change, growth activity
265
260
and emissions controls are more pronounced for
West Plains Midwest Northeast Southeast US
the PM2.5 concentrations than M8hO3 (Figures 4,
5). The US summer average concentrations for
Regions
Summers 2000-2002
90 Summers 2049-2051
80
70
Summers 2049-2051_np
5. REFERENCES
60 Byun, D. W., and J. K. S. Ching (Ed.) (1999),
M8hO3 (ppb)
50
40
Science algorithms of the EPA Models-3
30
20
Community Multiscale Air Quality Model (CMAQ)
10 modeling system, EPA/600/R-99/030, U.S.
Environ. Prot. Agency, Off. of Res. And Dev.,
0
West Plains Midwest Northeast Southeast US
Regions
Washington, D. C.
Carter, W. P. L. (2000), Documentation of the
Figure 4: Mean summer maximum eight (8) hour
SAPRC-99 Chemical Mechanism for VOC
O3 (M8hO3) concentrations for historic and future
Reactivity Assessment. Final Report to California
periods
Air Resources Board, Contract No. 92-329, and
95-308
3
Grell G., J. Dudhia and D. R. Stauffer (1994),
Summers_np
-14.8
-10.1
-11.7
A description of the fifth generation Penn
-7.7
-0.4
-5.5
0.7
8.7
5.8
State/NCAR mesoscale model (MM5), NCAR
OC (%)
Table 1: Mean summer changes (percentile) in pollutants concentrations for future periods compared to historic ones
Tech. Note, NCAR/TN-398+STR, Natl. Cent for
Atmos. Res., Boulder, Colorado
Summers
-27.5
-16.2
-19.1
-18.6
-25.2
-17.2
-6.7
-1.0
3.0
IPCC (Intergovernmental Panel on Climate
Change) (2000), Emissions Scenarios, Cambridge
University Press, Cambridge, UK
Summers_np
-13.3
-21.9
-12.2
-19.0
13.6
-6.9
-0.8
-47.9
-33.0
-41.8
-45.7
-34.3
-43.9
-29.8
-36.5
-44.5
-22.6
-53.7
-28.8
-7.8
-4.4
-77.1
-65.6
-53.4
-77.3
-79.3
-77.7
-16.4
-22.4
-16.5
-13.9
-17.8
-2.2
6.0
Louisiana
Summers
-48.7
-52.6
-60.5
-52.6
-32.8
-32.2
-29.8
-36.7
-56.7
Summers_np
-12.1
-18.4
-14.3
-15.9
11.8
-9.9
-2.0
-1.7
5.3
PM2.5 (%)
Summers
-37.1
-34.3
-45.2
-12.7
-35.9
-15.7
-32.4
-41.2
-5.1
Summers_np
-2.5
-0.1
-0.9
0.3
0.0
0.9
2.8
0.4
1.5
M8hO3 (%)
Summers
-24.4
-27.9
-18.9
-11.6
-15.8
-20.2
-10.7
-8.2
-6.5
Western Canada
Northern Mexico
Eastern Canada
Southeast
Northeast
Midwest
Plains
West
US