05.01.2013 Views

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

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

Concentrations and composition of <strong>PM2.5</strong><br />

3.6.2 Relationship of hourly mean <strong>PM2.5</strong> concentrations with air mass<br />

trajectory<br />

23. Back trajectories provide useful <strong>in</strong>formation on the orig<strong>in</strong> of an air mass and<br />

have been used to understand better the orig<strong>in</strong>s of <strong>PM2.5</strong> concentrations <strong>in</strong> the<br />

UK. An analysis has been carried out us<strong>in</strong>g HYSPLIT 96-hour back trajectories<br />

calculated for every three hours derived from NCEP/NCAR Reanalysis data<br />

(Draxler and Hess, 1997). The whole of each back trajectory, i.e. one every<br />

three hours, has been assigned the hourly mean <strong>PM2.5</strong> concentration for the<br />

arrival time at the arrival site. The same concentration is therefore associated<br />

with all the 96 hours preced<strong>in</strong>g the arrival time, giv<strong>in</strong>g 96 latitude/longitude<br />

locations along the trajectory with the arrival time concentration. For a large<br />

number of trajectories that cover widely different geographic regions, this<br />

technique provides an <strong>in</strong>dication of the source orig<strong>in</strong> of the pollutant be<strong>in</strong>g<br />

analysed. There are of course uncerta<strong>in</strong>ties <strong>in</strong> these calculations, for example <strong>in</strong><br />

the accuracy of the back trajectory calculations themselves. It must, however,<br />

be borne <strong>in</strong> m<strong>in</strong>d that any elevated concentrations at the arrival site will be<br />

assigned to all po<strong>in</strong>ts along the trajectory, even though the source may have<br />

only contributed at some <strong>in</strong>termediate po<strong>in</strong>t along the trajectory. The analysis<br />

of a large number of trajectories can, nevertheless, provide a good <strong>in</strong>dication of<br />

the geographic locations most strongly associated with elevated concentrations<br />

of <strong>PM2.5</strong>.<br />

24. As an example, Figure 3.12a shows the time series of daily mean <strong>PM2.5</strong><br />

concentrations at the Bexley Slade Green site <strong>in</strong> East London for 2009. It<br />

is apparent from this figure that there are clear periods when the <strong>PM2.5</strong><br />

concentrations are elevated, particularly <strong>in</strong> the first half of the year. The bottom<br />

plot, Figure 3.12b, shows the 96-hour back trajectories month by month at the<br />

Bexley site. The low concentrations <strong>in</strong> June-August tend to be associated with<br />

trajectories from the Atlantic and the north and the absence of trajectories from<br />

cont<strong>in</strong>ental Europe. Almost all the high concentration periods are associated<br />

with air mass trajectories from the east, although <strong>in</strong> some cases the pattern<br />

is complex. For example, <strong>in</strong> March 2009 there was a period of 4-5 days when<br />

anticyclonic conditions dom<strong>in</strong>ated to the east of the UK which set up circulatory<br />

air masses from cont<strong>in</strong>ental Europe. Such conditions would ensure that<br />

precursor emissions would have accumulated as air masses passed over areas of<br />

high precursor emission source strength, and this would have been comb<strong>in</strong>ed<br />

with sufficient time for secondary aerosol to be produced.<br />

25. The trajectory analysis has been extended to seven sites across the UK, as<br />

shown <strong>in</strong> Figure 3.13 for 2009 (the sites are broadly ordered from north to<br />

south). For clarity, the trajectory po<strong>in</strong>t concentrations have been smoothed<br />

to <strong>in</strong>dicate approximate source orig<strong>in</strong>s, similar to the work of Seibert et<br />

al. (1994) and Stohl (1996). The purpose of Figure 3.13 is to highlight the<br />

approximate spatial orig<strong>in</strong>s that contribute the highest <strong>PM2.5</strong> concentrations<br />

measured at the UK sites. There is consistency across the different sites <strong>in</strong> that<br />

the highest concentrations of <strong>PM2.5</strong> are dom<strong>in</strong>ated by air masses from the east<br />

and south-east. The higher background concentrations seen for the urban<br />

background Ed<strong>in</strong>burgh site <strong>in</strong> comparison with the rural Auchencorth Moss<br />

site will be due to local urban sources elevat<strong>in</strong>g the overall concentrations<br />

measured <strong>in</strong> Ed<strong>in</strong>burgh, irrespective of the trajectory direction. However, it is<br />

clear, for 2009 at least, that the contribution from ma<strong>in</strong>land Europe to high<br />

<strong>PM2.5</strong> concentrations at these northern UK sites is less than for sites further<br />

59

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!