[1] The Photochemical Activity and Ultraviolet Radiation (PAUR) II project (a continuation of an earlier PAUR I project) had the purpose of studying the interrelationships between changes in total ozone, tropospheric aerosols, UV radiation and photochemical activity. As part of PAUR II project, a campaign took place in Greece and Italy during MayJune 1999, with the participation of 15 European and 3 American research institutions. A variety of radiation and gaseous and aerosol atmospheric composition and optical characteristics measurements were made during the campaign. Radiative transfer models and three-dimensional (3-D) regional chemistry transport models (CTM) were applied and compared to the available data set of PAUR II. The present overview paper gives an introduction to the project and to the meteorological and environmental conditions that prevailed and outlines some results that are extensively described in the subsequent papers which form this special section. The modulation of the UVB field in the presence of different types of aerosols, its transmittance and role in the photochemistry of the particular eastern Mediterranean environment is overviewed. Using a 3-D CTM, it is shown that even a 50% reduction in Greek anthropogenic emissions has only a small effect in reducing the ozone levels over the eastern Mediterranean in summer. The environmental conditions, which prevailed during the PAUR I and PAUR II campaigns, offered cases of background conditions over the Aegean Sea as well as conditions with Saharan dust episodes and extremes in total ozone.

[1] Model studies show that changes in photodissociation rates resulting from changes in ozone column densities induce changes in lower tropospheric ozone, which vary significantly with location and time of the year. The validity of the model results is tested against daily total ozone and ground level ozone at three selected stations (Samoa, Mauna Loa, and Hohenpeissenberg). Observational data for a period of more than 1 decade have been analyzed. Comparisons are made of model-simulated distribution of ozone and its precursors (NO x and CO) at the three stations. Further comparisons are made of observed and model-calculated sensitivity in surface ozone to reduction in ozone column densities. Calculations performed with a global-scale chemical transport model (CTM) with extensive ozone chemistry reproduce well the observed levels and seasonal distribution of NO x , CO, and ozone at remote background stations (Samoa and Mauna Loa) and at stations in more polluted regions (Hohenpeissenberg). A chemical box model is used to demonstrate the chemical link between surface ozone changes and changes in total ozone for different NO x levels. Model studies and analysis of the observational data show that ground level ozone at the remote, low-NO x stations of Mauna Loa and Samoa is correlated positively with total ozone, with an exception at Mauna Loa during winter months. A reduction in ozone column densities, which leads to enhanced photochemical activity, reduces ozone levels at ground level. The sensitivity of surface ozone to changes in total ozone is particularly large in the low-NO x regime at Samoa. An anticorrelation between ground level ozone and total ozone is found at the Hohenpeissenberg station both in the observational data and in the model results during wintertime with high NO x levels. Enhanced photochemical activity leads to enhanced ozone production. There is, however, a disagreement between the observed and CTMmodeled sensitivity in surface ozone to ozone column density during the summer months at Hohenpeissenberg. The strong anticorrelation found in the observations, giving increases in surface ozone at low ozone column densities, is not present in the CTM model studies. It is suggested that a correlation between low ozone column densities and stagnant high-pressure systems is an important cause for the observed anticorrelation.

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[1] During the last 5 years, information on the regional tropospheric ozone levels over the eastern Mediterranean has become available but was confined to measurements at ground level. Here available information is expanded with measurements at two more rural ground level sites spanning 8°latitude, ozonesonde ascents, lidar observations, ship cruises, and aircraft flights. During wintertime the ozone monthly values are 10-20 ppbv higher than values at other European sites, while during summertime the values are comparable. This results in regional ozone background levels in the area that are above the European Union (EU) 32 ppb/24 hours phytotoxicity limit during the entire year. Late spring lidar observations show that south and southwestern synoptic flows which are associated with Saharan dust events result in lower ozone above the planetary boundary layer (PBL) by 20-35 ppbv as compared to these during northerly flows, which transport air from continental Europe. These lidar observations along with ship measurements during July show that ozone is enhanced 1.5-2.2 times in the continental outflow, when compared to aged maritime air or air from the African continent. These results along with ozonesonde observations suggest that ozone abatement in the area is largely beyond the control of regional emissions and can be controlled only with emission reductions on a European scale. During September, measured background NO and NO 2 levels between 3 and 4.5 km above sea level ranged from 1 to 221 pptv and from 102 to 580 pptv, respectively.