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
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
(c) The importance of secondary organic aerosol <strong>in</strong> assessments of air<br />
<strong>quality</strong>–climate <strong>in</strong>teractions has become more apparent s<strong>in</strong>ce the 2007<br />
AQEG report. However, there are now open questions concern<strong>in</strong>g<br />
biogenic versus anthropogenic sources. For example, there is some<br />
evidence that a major fraction of organic aerosol (OA) may be derived<br />
from anthropogenically modified biogenic volatile organic compounds<br />
(i.e. biogenic secondary OA is formed preferentially <strong>in</strong> polluted<br />
environments). Understand<strong>in</strong>g such l<strong>in</strong>ks is highly relevant to policy<br />
measures because it means that changes <strong>in</strong> gas phase pollutants<br />
(NOx, ozone, etc.) might impact PM and aerosol forc<strong>in</strong>g. The impact of<br />
climate on biogenic emissions is still an open question.<br />
(d) It is important to review our understand<strong>in</strong>g of how the aerosol system<br />
will respond to changes <strong>in</strong> anthropogenic emissions and to <strong>in</strong>tegrate<br />
our knowledge about PM and climate-relevant particles. It is important<br />
to understand how PM concentrations and climate-relevant particles<br />
might respond differently to chang<strong>in</strong>g emissions. The future trajectory of<br />
anthropogenic secondary organic aerosol (SOA) is very uncerta<strong>in</strong> because<br />
of changes <strong>in</strong> the nature of the emissions as well as the response of SOA<br />
to atmospheric chemistry changes (NOx, ozone, etc.). Changes <strong>in</strong> some<br />
emissions are likely to have a large effect on particle mass but a small<br />
effect on number (e.g. non-nucleat<strong>in</strong>g semi-volatile species or large<br />
primary particles), while for some emissions the opposite may be true<br />
(e.g. emissions of numerous small particles from combustion that may<br />
affect climate but not PM). These climate and air <strong>quality</strong> issues should be<br />
considered <strong>in</strong> an <strong>in</strong>tegrated way.<br />
(e) Climate change will exert a potentially important upward pressure on PM<br />
for many reasons that are not well understood. The effects of climate<br />
change on PM and climate-relevant particle number concentrations<br />
should be assessed, recognis<strong>in</strong>g that these parameters may behave<br />
differently. Also, it would be useful to understand the importance of:<br />
(i) changes <strong>in</strong> atmospheric circulation patterns which will affect the<br />
occurrence of block<strong>in</strong>g anticyclonic weather (and the build-up of PM<br />
extremes);<br />
(ii) temperature <strong>in</strong>creases caus<strong>in</strong>g greater biogenic VOC emissions and<br />
consequently <strong>in</strong>creased biogenic SOA;<br />
Introduction<br />
(iii) changes <strong>in</strong> removal processes, primarily wet scaveng<strong>in</strong>g. This is likely to<br />
dom<strong>in</strong>ate future changes <strong>in</strong> PM, but maybe only on a long-term average<br />
basis with little effect on PM extremes; and<br />
(iv) changes <strong>in</strong> atmospheric chemistry affect<strong>in</strong>g oxidants, nitrate formation<br />
and SOA chemistry.<br />
17