Air quality expert group - Fine particulate matter (PM2.5) in ... - Defra
Air quality expert group - Fine particulate matter (PM2.5) in ... - Defra
Air quality expert group - Fine particulate matter (PM2.5) in ... - Defra
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<strong>PM2.5</strong> <strong>in</strong> the UK<br />
102<br />
measurements and gas phase pollutant data <strong>in</strong> the model will also assist<br />
<strong>in</strong> identify<strong>in</strong>g the location of sources. The comb<strong>in</strong>ed dataset of sizeresolved<br />
and chemically-speciated particle concentrations, together with<br />
meteorological data and gaseous pollutant concentrations, will be a very<br />
powerful probe <strong>in</strong>to the sources.<br />
65. Receptor modell<strong>in</strong>g <strong>in</strong> Europe has used a number of methods and lacks overall<br />
co-ord<strong>in</strong>ation (Viana et al., 2008). Compositional data for PM10 and <strong>PM2.5</strong><br />
are available from a sizeable number of European sites (Putaud et al., 2010),<br />
but there have been rather few substantial studies <strong>in</strong> Europe, largely because<br />
of the lack of suitable measurement datasets. One of the best recent studies<br />
(Mooibroek et al., 2011) applied the multivariate PMF method to <strong>PM2.5</strong> data<br />
from the Netherlands, generat<strong>in</strong>g a seven factor solution. The sources identified<br />
were nitrate-rich secondary aerosol, sulphate-rich secondary aerosol, traffic and<br />
resuspended road dust, <strong>in</strong>dustrial (metal) activities/<strong>in</strong>c<strong>in</strong>eration, sea spray, crustal<br />
material and residual oil combustion. The necessary comprehensive chemical<br />
composition datasets for UK sites are very limited and the only substantial study<br />
is Y<strong>in</strong> et al. (2010) which applied the chemical mass balance (CMB) model<br />
to specially collected datasets from one urban and one rural site <strong>in</strong> the West<br />
Midlands.<br />
66. The ma<strong>in</strong> advantage of the CMB model is that unlike multivariate models,<br />
no deductions are needed to establish the identity of sources. The model is<br />
able to quantify unassigned mass and therefore gives a clear <strong>in</strong>dication, not<br />
readily available from the multivariate models, of whether sources are miss<strong>in</strong>g.<br />
One of the ma<strong>in</strong> weaknesses of the CMB modell<strong>in</strong>g approach is the need for<br />
locally relevant source profiles, which are frequently not available from recent<br />
measurements <strong>in</strong> Western Europe. Consequently, source chemical profiles<br />
from North America are used and these may not be wholly representative of<br />
UK sources, hence contribut<strong>in</strong>g to error. Another ma<strong>in</strong> weakness is that CMB<br />
can only account for those sources which are <strong>in</strong>cluded and, whilst as <strong>in</strong>dicated<br />
above it will quantify unassigned mass, it will give no clues as to the orig<strong>in</strong>s of<br />
that mass. In addition, CMB does not readily account for secondary pollutants<br />
or for the chemical modification of primary pollutants between source and<br />
receptor.<br />
67. The ma<strong>in</strong> advantage of multivariate statistical models is that they are able to<br />
take account of secondary pollutants or chemical change between source and<br />
receptor and require no a priori knowledge of the contribut<strong>in</strong>g sources or their<br />
source profiles. On the other hand, there are disadvantages follow<strong>in</strong>g from<br />
an <strong>in</strong>ability to dist<strong>in</strong>guish sources of similar composition or sources whose<br />
concentrations vary <strong>in</strong> a similar manner. It is notable from the literature that<br />
many of the source signatures generated by multivariate methods are extremely<br />
difficult to assign unequivocally to a given source type. This leads to uncerta<strong>in</strong><br />
assignments and the problems which flow from that.<br />
4.5.1 Markers of primary sources<br />
68. There are few sources for which a s<strong>in</strong>gle chemical tracer can be used as a<br />
marker. Frequently sources can only be identified and quantified by use of a<br />
comb<strong>in</strong>ation of chemical components. Commonly used elemental tracers are<br />
silicon or alum<strong>in</strong>ium (soil and crustal dust), sodium (sea salt), barium (vehicular