From hygroscopic aerosols to cloud droplets: The HygrA-CD campaign in the Athens basin - An overview.

The international experimental campaign Hygroscopic Aerosols to Cloud Droplets (HygrA-CD), organized in the Greater Athens Area (GAA), Greece from 15 May to 22 June 2014, aimed to study the physico-chemical properties of aerosols and their impact on the formation of clouds in the convective Planetary Boundary Layer (PBL). We found that under continental (W-NW-N) and Etesian (NE) synoptic wind flow and with a deep moist PBL (~2-2.5km height), mixed hygroscopic (anthropogenic, biomass burning and marine) particles arrive over the GAA, and contribute to the formation of convective non-precipitating PBL clouds (of ~16-20µm mean diameter) with vertical extent up to 500m. Under these conditions, high updraft velocities (1-2ms-1) and cloud condensation nuclei (CCN) concentrations (~2000cm-3 at 1% supersaturation), generated clouds with an estimated cloud droplet number of ~600cm-3. Under Saharan wind flow conditions (S-SW) a shallow PBL (<1-1.2km height) develops, leading to much higher CCN concentrations (~3500-5000cm-3 at 1% supersaturation) near the ground; updraft velocities, however, were significantly lower, with an estimated maximum cloud droplet number of ~200cm-3 and without observed significant PBL cloud formation. The largest contribution to cloud droplet number variance is attributed to the updraft velocity variability, followed by variances in aerosol number concentration.

Severe particulate pollution from the deposition practices of the primary materials of a cement plant.

Global cement production has increased twofold during the last decade. This increase has been accompanied by the installation of many new plants, especially in Southeast Asia. Although various aspects of pollution related to cement production have been reported, the impact of primary material deposition practices on ambient air quality has not yet been studied. In this study, we show that deposition practices can have a very serious impact on levels of ambient aerosols, far larger than other cement production-related impacts. Analyses of ambient particulates sampled near a cement plant show 1.3-30.4 mg/m(3) total suspended particulates in the air and concentrations of particles with a diameter of 10 µm or less at 0.04-3 mg/m(3). These concentrations are very high and seriously exceed air quality standards. We unequivocally attribute these levels to outdoor deposition of cement primary materials, especially clinker, using scanning electron microscopy/energy-dispersive X-ray spectroscopy. We also used satellite-derived aerosol optical depth maps over the area of study to estimate the extent of the spatial impact. The satellite data indicate a 33% decrease in aerosol optical depth during a 10-year period, possibly due to changing primary material deposition practices. Although the in situ sampling was performed in one location, primary materials used in cement production are common in all parts of the world and have not changed significantly over the last decades. Hence, the results reported here demonstrate the dominant impact of deposition practices on aerosol levels near cement plants.

Transport of toxic organic aerosol pollutants from Yugoslavia to Greece during the operation "Allied Force".

Between March 24 and June 10, 1999 a large number of chemicals were ejected into the atmosphere because of air strikes on chemical industries and oil storage facilities in former Yugoslavia. Chemicals released into the atmosphere under suitable meteorological conditions can be transported across borders to large distances. The releases may have contained not only conventional air pollutants but also semi-volatile organic compounds (SOCs) which include dioxins, furans, PCBs and PAHs, all known to be hazardous to health. A measuring programme was initiated at Democritus University Thrace, Greece to monitor the chemical characteristics of atmospheric aerosol during February, March and April 1999. Particulate matter (aerosol) was collected on filters and was analysed using high-resolution gas chromatography coupled to high-resolution mass spectrometry for their content in SOCs. In the present work we show evidence of two events with three to twenty fold increased SOCs in the atmosphere of Northern Greece which were associated with air masses transported from the conflict area, following the destruction of chemical plants and oil storage facilities.

The war in Kosovo: Evidence of pollution transport in the Balkans during operation "Allied Force".

During the operation "Allied Force" in the spring of 1999, the burning or damaging of industrial and military targets in the Former Republic of Yugoslavia resulted in the release of a large number of chemicals into the atmosphere. The releases contained not only conventional air pollutants, but also Semi-Volatile Organic compounds (SVOs) which are known to be hazardous to health. Under suitable meteorological conditions, these chemicals can be transported across borders over large distances. In this paper, an analysis of measurements and dispersion calculations is presented which provides evidence of pollutant transport from the conflict area to Greece. The measuring program was carried out in Xanthi, Greece and included aerosol sampling and subsequent analysis for the determination of the concentration of SVOs including dioxins, furans, PCBs (PolyChlorinated Biphenyls), PAHs (Polycyclic Aromatic Hydrocarbons) and organic phthalates. This paper focuses on two episodes of organic phthalates that were observed during the conflict period. Pollution measurements are interpreted by means of air trajectories and dispersion calculations. For this purpose, the HYSPLIT_4 (HYbrid Single-Particle Langrangian Integrated Trajectory) modeling system is used to calculate the dispersion of toxic substances.

Correcting global solar ultraviolet spectra recorded by a brewer spectroradiometer for its angular response error.

We present a methodology for correcting the global UV spectral measurements of a Brewer MKIII spectroradiometer for the error introduced by the deviation of the angular response of the instrument from the ideal response. This methodology is applicable also to other Brewer spectroradiometers that are currently in operation. The various stages of the methodology are described in detail, together with the uncertainties involved in each stage. Finally global spectral UV measurements with and without the application of the correction are compared with collocated measurements of another spectroradiometer and with model calculations, demonstrating the efficiency of the method. Depending on wavelength and on the aerosol loading, the cosine correction factors range from 2% to 7%. The uncertainties involved in the calculation of these correction factors were found to be relatively small, ranging from ~0.2% to ~2%.

Optical properties of tropospheric aerosols determined by lidar and spectrophotometric measurements (Photochemical Activity and Solar Ultraviolet Radiation campaign).

We present the results of the aerosol measurements carried out over the Aegean Sea during the Photochemical Activity and Solar Ultraviolet Radiation campaign held in Greece during June 1996. Simultaneous observations performed with a lidar and a double-monochromator spectrophotometer allowed us to retrieve the optical depth, the Angström coefficient, and the backscatter-to-extinction ratio. The Sun photometric data can be used to improve quantitative aerosol measurements by lidar in the Planetary Boundary Layer. Systematic errors could arise otherwise, because the value of the backscatter-to-extinction ratio has to be supplied. Instead this ratio can be retrieved experimentally by use of an iterative solution of the lidar equation.

Measured trends in stratospheric ozone.

Recent findings, based on both ground-based and satellite measurements, have established that there has been an apparent downward trend in the total column amount of ozone over mid-latitude areas of the Northern Hemisphere in all seasons. Measurements of the altitude profile of the change in the ozone concentration have established that decreases are taking place in the lower stratosphere in the region of highest ozone concentration. Analysis of updated ozone records, through March of 1991, including 29 stations in the former Soviet Union, and analysis of independently calibrated satellite data records from the Total Ozone Mapping Spectrometer and Stratospheric Aerosol and Gas Experiment instruments confirm many of the findings originally derived from the Dobson record concerning northern midlatitude changes in ozone. The data from many instruments now provide a fairly consistent picture of the change that has occurred in stratospheric ozone levels.