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288<br />

Impact of megacities on the regional air quality: A South American case<br />

study<br />

Claas Teichmann and Daniela Jacob<br />

Max-Planck-Institute for Meteorology, Hamburg, claas.teichmann@zmaw.de<br />

1. Introduction<br />

Natural as well as anthropogenic emissions determine the<br />

aerosol and chemical composition of the atmosphere.<br />

This has a major impact on cloud formation, on the<br />

hydrological cycle and on air quality. In many South<br />

American regions the effects of megacities - such as São<br />

Paulo, Buenos Aires, etc. - are crucial and have an impact<br />

on a regional scale. In other regions the emissions are<br />

dominated by natural sources as well as by land-use<br />

change and biomass burning. The goal of the study is to<br />

estimate the impacts of different emission sources on the<br />

regional air quality.<br />

In South America the Andes have a significant influence<br />

on the atmospheric circulation and on the transport of<br />

chemical species, because of the pronounced orographic<br />

features. An adequate representation of the Andes within<br />

a climate model is only possible with the relatively high<br />

horizontal resolution of a regional climate model. The<br />

high resolution is also needed to resolve the megacities<br />

with their highly concentrated emissions and the<br />

corresponding chemical reactions.<br />

2. The regional model REMO including online<br />

chemistry and tracer transport<br />

In this study the newest operational version of the<br />

regional climate model REMO (Jacob et al., 2001, 2007)<br />

is used including on-line chemistry and tracer transport.<br />

The chemistry module is based on the second generation<br />

Regional Acid Deposition Model (RADM2) (Stockwell et<br />

al., 1990).<br />

The model calculates the meteorological processes<br />

directly together with photochemistry and tracer<br />

transport. The advantage over off-line chemistrytransport<br />

models – which are driven by the, e.g., hourly<br />

output from a meteorological model – is the direct<br />

coupling of meteorological and chemical fields, which<br />

both are available for each model timestep.<br />

In the current model setup, the atmospheric mechanisms<br />

influence the chemical mechanism and the tracer<br />

transport, while there is no feedback from chemistry and<br />

tracer concentrations onto the atmospheric properties and<br />

processes (see Fig 1).<br />

Fig 1. REMO with chemistry and tracer transport<br />

The advantage of this setup is that different case studies,<br />

e.g., with modified emission inventories, are subject to<br />

exactly the same meteorological conditions. Differences<br />

in resulting trace gas concentrations can be attributed to<br />

the chemical mechanism and to the modifications made,<br />

e.g., to the emission inventory.<br />

3. Boundary data<br />

Boundary and initial data for the chemical species<br />

concentrations is provided by global model output from<br />

the Model for Ozone and Related Chemical Tracers<br />

(MOZART) (Kinnison et al., 2007). Anthropogenic<br />

emission data and fire emission data is taken from the<br />

REanalysis of the TROpospheric chemical composition<br />

over the past 40 years (RETRO) emission database (e.g.,<br />

Schultz et al., 2008).<br />

Meteorological boundary conditions are provided by<br />

ERA-40 re-analysis data (Uppala et al.,2005).<br />

4. Model simulations<br />

In order to assess the impact of the different emission<br />

sources, several model runs are performed in a case study<br />

for the year 2000. They include the full chemistry and<br />

tracer transport and are embedded in a hindcast which<br />

comprises the whole ERA-40 period for meteorology<br />

only.<br />

A so called reference run includes the full emission<br />

inventory, natural as well as anthropogenic emissions. In<br />

two sensitivity runs the emissions from different sources<br />

are modified.<br />

Emissions from eight megacities (cities with more than<br />

five million inhabitants) are reduced by 90% in the first<br />

sensitivity run (denoted as reduced megacity emissions<br />

run). In the second sensitivity run, denoted as no-fires<br />

run, fire emissions are removed from the emission<br />

inventory. In a comparison, the impact of the different<br />

emission sources on the regional air quality is obtained.<br />

5. Results<br />

As an example, results from two sensitivity runs are<br />

shown for the simulated April 2000. As April is not part<br />

of the main fire season, the impact of the fire-emissions is<br />

relatively low, compared to the maximum fire impact of<br />

the year.<br />

In Figure 2 the maximum weighted difference between<br />

the sensitivity runs and the reference run of near surface<br />

CO concentrations (lowest model layer) is shown for the<br />

reduced megacity emissions run. Figure 3 shows the<br />

maximum weighted difference of CO concentrations for<br />

the no-fires run. This gives an impression of the extent of<br />

air pollution episodes originating from megacities<br />

compared to fire emissions and shows which regions are<br />

affected.<br />

As South American megacities are located mainly in<br />

coastal regions, pollution can be transported long<br />

distances over the ocean. This is shown for Buenos Aires<br />

where the CO pollution plume reaches far over the<br />

southern Atlantic with a relative impact (i.e., the increase<br />

from the reduced megacity emissions to the reference<br />

case) of more than 10%.

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