In order to evaluate the possible effects of heatwave phenomena on background O3 concentrations, the average summer O3 concentrations at the high mountain station of Mt. Cimone (MTC—2165 m a.s.l.) have been analyzed. In particular, at this baseline station unusually high O3 concentrations were recorded during August 2003, when an intense heatwave (the “August heatwave”) affected Europe. During this heatwave, the highest O3 concentrations were recorded at MTC in connection with air masses coming from continental Europe and the Po basin boundary layer as shown by three-dimensional air mass back-trajectory and mixing height analyzes. However, high O3 concentrations were also recorded in air masses coming from the middle troposphere (above 3000 m a.s.l.), thus suggesting the presence of O3-rich atmospheric layers over Europe. This could be due to the large extension of the mixing layer which favoured the transport of high concentrations of O3 and its precursors to altitudes that would usually be in the free troposphere. Other than from traffic and industrial activities, a contribution to the high O3 concentrations recorded at MTC during the August heatwave could derive from fires in the North of Italy, as suggested by a well-documented episode and supported by in situ CO2 measurements used as non-conventional tracer for fire emissions.

High altitude mountaintop observatories provide the opportunity to study aerosol properties in the free troposphere without the added expense and difficulty of making airborne measurements. Over the last several decades the number of mountaintop observatories continuously measuring in-situ aerosol radiative properties has increased significantly from a single station (Mauna Loa, USA) in the 1970's to at least ten observatories actively making these measurements today. By taking this data set as a whole and developing a self-consistent climatology, the combined observatory measurements of free tropospheric aerosol radiative properties have the potential to contribute to aerosol-climate research in a way that far exceeds the contribution from individual observatories. For example, this type of analysis may help constrain chemical transport models, validate satellite measurements, and quantify the influence of smoke and dust episodes on free troposphere aerosol properties. Here we present statistics of means, variability, and trends of aerosol radiative properties, including light scattering, light absorption, light extinction, single scattering albedo, Ångström exponent, hemispheric backscatter fraction and radiative forcing efficiency, from various high altitude measurements. These climatologies utilize data from ten mountaintop observatories in the 20-50ºN latitude band: Mauna Loa, USA; Lulin Mountain, Taiwan; Pyramid, Nepal; Izaña, Spain; Mount Waliguan, China; Beo Moussala, Bulgaria; Mount Bachelor, USA; Monte Cimone, Italy; Jungfraujoch, Switzerland; Whistler Mountain, Canada. Results are also included from two multi-year, in-situ aerosol vertical profiling programs: Southern Great Plains, USA and Bondville, USA. Using this cloud- and boundary layer contamination- screened data set we address the following questions: (1) What are the similarities and differences in the means, variability and trends of free-tropospheric aerosol radiative properties at a wide range of locations? (2) What is the relative importance of aerosol amount and aerosol optical properties for direct radiative forcing calculations? Delene and Ogren (2002) showed that the amount of aerosol was of primary importance while the aerosol optical properties were of secondary importance to direct radiative forcing calculations for the four boundary layer sites they studied. (3) How do these in-situ climatologies of free tropospheric light extinction compare to the satellite-derived climatologies presented by Kent et al., 1998? (4) Do aerosol events (e.g., smoke transport) have a significant influence on climatological values?