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Air quality expert group - Fine particulate matter (PM2.5) in ... - Defra

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Table 5.3: Population-weighted annual mean <strong>PM2.5</strong> concentrations (µg m -3 ) calculated us<strong>in</strong>g<br />

the PCM model for different parts of the UK.<br />

2009 2010 2015 2020<br />

Scotland 6.83 6.61 6.14 5.85<br />

Wales 8.95 8.62 8.02 7.64<br />

Northern Ireland 7.27 6.93 6.35 5.98<br />

Inner London 15.05 14.47 13.26 12.59<br />

Outer London 13.91 13.37 12.28 11.67<br />

Rest of England 10.80 10.39 9.61 9.13<br />

UK 10.70 10.29 9.51 9.04<br />

5.4.2 Secondary <strong>in</strong>organic aerosol<br />

Modell<strong>in</strong>g <strong>PM2.5</strong> and the future<br />

29. The secondary <strong>in</strong>organic aerosol (SIA) <strong>in</strong> the form of sulphate (SO4 2- ), nitrate<br />

(NO3 - ) and ammonium (NH4 + ) <strong>particulate</strong>s is formed from precursor emissions<br />

of SO2, NOx and NH3. Most of the SIA is with<strong>in</strong> the <strong>PM2.5</strong> range, and gives a<br />

contribution to population exposure several times greater than primary <strong>PM2.5</strong><br />

emissions, although there are questions as to whether this component is as<br />

toxic as some of the primary material. The modell<strong>in</strong>g of SIA components is<br />

complicated by the chemical <strong>in</strong>teraction between pollutants, result<strong>in</strong>g <strong>in</strong> the<br />

formation of ammonium sulphate and ammonium nitrate, as well as a coarser<br />

nitrate component of SIA. The formation of ammonium nitrate <strong>particulate</strong><br />

<strong>matter</strong> is reversible, with models frequently assum<strong>in</strong>g an equilibrium between<br />

gaseous and <strong>particulate</strong> states depend<strong>in</strong>g on ambient NH3 and nitric acid<br />

(HNO3) concentrations. This system is extremely difficult to model given the<br />

highly variable emissions of NH3 spatially and temporally, and hence the very<br />

patchy and <strong>in</strong>termittent pattern of NH3 concentrations. These NH3 emissions<br />

arise predom<strong>in</strong>antly <strong>in</strong> rural areas from agricultural activities, but there are also<br />

some urban sources, <strong>in</strong> particular from some vehicle exhausts (see Chapter 4).<br />

30. The chemical <strong>in</strong>teractions between pollutants result <strong>in</strong> a complex response<br />

to the reduction of pollutant emissions, for example a change <strong>in</strong> NOx or SO2<br />

emissions can affect NH4 + concentrations as well as NO3 - and SO4 2- , depend<strong>in</strong>g<br />

on the mix of pollutants. This results <strong>in</strong> a non-l<strong>in</strong>ear relationship, whereby<br />

percentage changes <strong>in</strong> NO3 - , SO4 2- and NH4 + are not directly proportional to<br />

percentage changes <strong>in</strong> NOx, SO2 and NH3 emissions respectively. However,<br />

source–receptor relationships, derived from more complex models by estimat<strong>in</strong>g<br />

the change <strong>in</strong> SIA concentration at receptor po<strong>in</strong>ts <strong>in</strong> response to small<br />

reductions of one pollutant at a time from each emitt<strong>in</strong>g source, are often used<br />

as a l<strong>in</strong>ear approximation <strong>in</strong> simpler modell<strong>in</strong>g approaches to analyse different<br />

emission scenarios. This is the approach used <strong>in</strong> <strong>in</strong>tegrated assessment models<br />

such as GAINS and UKIAM, avoid<strong>in</strong>g the need to run a complex model such as<br />

EMEP or CMAQ for each new scenario, but <strong>in</strong>troduc<strong>in</strong>g <strong>in</strong>creas<strong>in</strong>g uncerta<strong>in</strong>ties<br />

133

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