PM10 and heavy metal measurements in an industrial area of southern Italy

Atmospheric particulate concentrations and heavy metal content are measured from March to July 2001 at an industrial site located in a rural zone of the southern Italy. PM₁₀ samples are collected by a low-volume sampler and each sample is analysed by AAS techniques for its content of Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn. We measure also temperature, atmospheric pressure and relative humidity, and we collect anemometric data. The study purpose is the investigation of pollutant levels in an industrial area located in a rather unpolluted region and the characterization of the correlation structure among particulate concentrations, heavy metal content and local meteorological parameters. Data analysis is carried out by means of univariate and multivariate statistical methods. In the investigated period, the average value of PM₁₀ daily concentrations (24 μg Nm^− 3) does not exceed the national standard of 40 μg Nm^− 3 and only nine values are higher than the European daily limit value of 50 μg Nm^− 3. Particularly, the occurrence of two anomalous values (183 μg Nm^− 3 in 3 March and 94 μg Nm^− 3 in 22 June) seems to be related to no-local events as confirmed both by in situ data measured in the AQM network of Potenza city (about 10 km far from the study area) and by remote measurements performed in the same days. Regarding the heavy metal levels, we observe high levels of Cr (34 ng Nm^− 3), Ni (85 ng Nm^− 3) and Zn (214 ng Nm^− 3) in agreement with the local industrial source pattern. The multivariate analysis, carried out using meteorological parameters as exogenous variables, allow to evaluate the role of the different variables as driving factors of the correlation structure among the metals.     

Characteristics of biomass burning aerosol and its impact on regional air quality in the summer of 2003 at Gwangju, Korea

The main objective of this study is to investigate the chemical characteristics of biomass burning aerosol and its impact on regional air quality during an agricultural waste burning period in early summer in the rural areas of Korea. A 12-h integrated intensive sampling of biomass burning aerosol in the fine and coarse modes was conducted on 2–20 June 2003 in Gwangju, Korea. The collected samples were analyzed for concentrations of mass, ionic, elemental, and carbonaceous species. Average concentrations of fine and coarse mass were measured to be 67.9 and 18.7 μg m^− 3 during the biomass burning period, 41.9 and 18.8 μg m^− 3 during the haze period, and 35.6 and 13.3 μg m^− 3 during the normal period, respectively. An exceptionally high PM_2.5 concentration of 110.3 μg m^− 3 with a PM_2.5/PM₁₀ ratio of 0.79 was observed on 6 June 2003 during the biomass burning period. The potassium ratio method was used to identify biomass burning samples. The average ratio of potassium in the fine mode to the coarse mode (FK/CK) was 23.8 during the biomass burning period, 6.0 during the haze period, and 4.7 during the normal period, respectively. A FK/CK ratio above 9.2 was considered a criterion for biomass burning event in this study. Particulate matter from the open field burning of agricultural waste has an adverse impact on visibility, human health, and regional air quality.     

Changes of cloud water chemical composition in the Western Sudety Mountains, Poland

The changing chemical composition of cloud water and precipitation in the Western Sudety Mountains are discussed against the background of air-pollution changes in the Black Triangle since the 1980s until September 2004. A marked reduction of sulphur dioxide emissions between the early 1990's and the present (from almost 2 million tons to around 0.2 million tons) has been observed, with a substantial decline of sulphate and hydrogen concentration in cloud water (SO₄²⁻ from more than 200 to around 70 μmol l^− 1; H⁺ from 150 to 50 μmol l^− 1) and precipitation (SO₄²⁻ from around 80 to 20–30 μmol l^− 1; H⁺ from around 60 to 10–15 μmol l^− 1) samples. At some sites, where fog/cloud becomes the major source of pollutants, deposition hot spots are still observed where, for example, nitrogen deposition can exceed 20 times the relevant critical load. The results show that monitoring of cloud water chemistry can be a sensitive indicator of pollutant emissions.     

Pollutant concentrations in fog and low cloud water at selected sites of the Czech Republic

In this paper, the basic composition of fog and low cloud water are presented, resulting from the analyses of water samples from 111 fog/cloud events. The samples were collected at five sites located in various regions of the Czech Republic. Two sampling sites are in mountainous regions and three sites represent various urban areas. The mountain stations are located in two regions of the Czech Republic with different industry types. At all the sites, active fog collectors were employed. In the water samples, the conductivity, acidity (pH), cations (H⁺, Na⁺, K⁺, NH₄⁺, Mg²⁺, Ca²⁺) and anions (F⁻, Cl⁻, NO₃⁻, SO₄²⁻) were determined.A mean pH value of about 4.5 was obtained at mountain sites whereas the measurements in urban areas showed mean pH values from 4.9 to 6.4. The mean conductivity values in the samples from the two mountain stations were 137 and 191.5 μS cm⁻¹. The samples from urban sites showed mean values between 127.7 and 654.4 μS cm⁻¹. The maximum concentration means for the three dominant pollutants (expressed by the ratio mountain sites/urban sites) are 32.9/99.6 mg l⁻¹ for NO₃⁻, 32.5/192.9 mg l⁻¹ for SO₄²⁻ and 18.5/52.7 mg l⁻¹ for NH₄⁺. As expected, we found higher ion concentrations in the northern part of the Czech Republic where larger numbers of lignite-burning power plants, chemical factories and opencast lignite mines are located. A decrease in ion concentrations was observed at higher altitude sites, probably reflecting at least in part higher liquid water contents at these locations.     

Major ionic composition of precipitation in the Nam Co region, Central Tibetan Plateau

A total of 48 precipitation samples have been collected from individual precipitation events at the Nam Co Monitoring and Research Station for Multisphere Interactions (Nam Co Station, 30°47′N, 90°58′E; 4730 m a.s.l) located in the central Tibetan Plateau from August 2005 to August 2006. All samples were analyzed for major cations (NH₄⁺, Na⁺, K⁺, Ca²⁺ and Mg²⁺) and anions (Cl⁻, NO₃⁻ and SO₄²⁻), conductivity and pH. Precipitation pH values ranged from 6.03 to 7.38 with an average value of 6.59. The high pH is due to large inputs of crustal aerosols in the atmosphere, which contain a large fraction of carbonate. Ca²⁺ is the dominant cation in precipitation with an average value of 65.58 μeq L^− 1 (4.91–301.41 μeq L^− 1), accounting for 54% of the total cations in precipitation. HCO₃⁻ is the predominant anion, accounting for 62% of the total anions. When compared with data from a snow pit in the Zhadang Glacier 50 km away (5800 m a.s.l), major ion concentration in precipitation at the Nam Co Station is much higher due to local aerosol inputs. Correlation and empirical orthogonal function (EOF) analysis indicate that regional crustal aerosols and species from combustion emissions of residents are the major sources for these ions, lake salt aerosols from the Nam Co nearby and regional mineral aerosols from dry lake sediments are secondary sources, and sea salt contribution is the least due to the long distance transport.     

Black carbon relationships with emissions and meteorology in Xi'an, China

Aerosol black carbon (BC) was measured every 5 min at Xi'an, China from September 2003 to August 2005. Daily BC concentrations ranged from 2 to 65 μg m^− 3, averaging 14.7 ± 9.5 μg m^− 3 and displayed clear summer minima and winter maxima. BC typically peaked between 0800 and 1000 LST and again between 2000 and 2200 LST, corresponding with morning and evening traffic combined with nighttime residential cooking and heating. The nocturnal peak was especially evident in winter, when more domestic heating is used and pollutant-trapping surface-inversions form earlier than in summer. BC frequency distributions the most commonly occurring concentrations occurred between 5 and 10 μg m^− 3 in all four seasons. BC ranged from 1.6% and 15.6%, and averaged 8.3% of PM_2.5. A clear inverse relationship between BC and wind speed (WS) was found when WS was below 2.5 to 3.0 m s^− 1, implying a local origin for BC. Mixed layer depths (MLDs) were shallower during BC episodes compared to cleaner conditions.     

An airborne two-stage impactor for chemical analysis of size-segregated cloud drops

Aqueous concentrations of ionic species observed in cloud water studies often have been in conflict with expectations from model predictions. These inconsistencies result from the size-dependent chemical composition of cloud drops during different stages in the lifetime of a cloud. To study this phenomenon, droplets of clouds need to be collected in different size ranges with high resolution in space and time. The only possibility for this kind of study is the use of an aircraft. Therefore, during the last several years, an attempt was made to develop a mobile cascade impactor, which can be installed outside an aircraft. The cloud water sampled in different size fractions can be transferred into the interior of the aircraft during the measuring flight. The collector is able to sample two size fractions. For continental clouds, the cutoffs are chosen to be >5 and >13.5 μm in diameter. For maritime clouds, the cutoff for the first stage could be shifted to 18.6 μm by lowering the nozzle speed. Prior to field application, the collector was characterized with the aid of “calibration fogs” produced in the laboratory with different drop sizes and different chemical compositions. The characterization included the examination of the cutoffs and the reliability of the sampling procedure with regard to the subsequent chemical analysis. With a collection period of 2 min, collection rates in the order of 0.1–1 cm³ min⁻¹ can be obtained. The collector characterized in this manner was successfully used during measuring flights in clouds over northern Germany. Preliminary concentrations of NH₄⁺, SO₄²⁻ and Cl⁻ found in the two size fractions of the cloud drops are presented.     

Atmospheric observations of liquid water in cloud and of chemical species in aerosols and gases near the ground and in fallen snow at Svalbard, Arctic

Columnar observations of liquid water and of radar echo intensity in cloud were carried out, using a microwave radiometer and a vertically pointing radar respectively, in Ny-Ålesund, Svalbard. Chemical concentrations were also measured in aerosols, gases and snowfalls. Clouds with a large proportion of liquid water moved over the site after snow clouds, with a much lower liquid water content, had been present for about 16 h. The mass concentrations of most chemical species in snowfalls were lower from the first set of clouds than the second. The NO₃⁻ and SO₄²⁻ concentrations in gases and aerosols associated with the first set of clouds were higher than in the second set, but Cl⁻ concentration was less for the first set than the second.     

Traffic aerosols (18 nm particle size 18 μm) source apportionment during the winter period

In November 2004–January 2005, a micro orifice uniform deposit impactor (MOUDI) and a Nanometer (nanometer)-MOUDI were used in the center of Taiwan to measure particle size (18 nm particle size 18 μm) distributions of atmospheric aerosols at a traffic site during the winter period. The average Mass in Media Aerodynamic Diameter (MMAD) of suspended particles is 0.99 μm this study. As for the ultra fine and nanometer (nanometer) particle mode, the composition order for these major ions species was SO₄²⁻ NH₄⁺ NO₃⁻ Mg²⁺ Ca²⁺ Na⁺ K⁺ Cl⁻. An ion Chromatography (DIONEX-100) was used to analyze major anion species, Cl⁻, NO₃⁻, SO₄²⁻ and cation species, NH₄⁺Na⁺, K⁺, Ca²⁺Mg²⁺. Their concentrations were also extracted from various particles size modes (nanometer (nanometer), ultra fine, fine and coarse). The results obtained in this study also indicated that the average portions for the major ionic species (SO₄²⁻, NH₄⁺ and Mg²⁺) in the nanometer (nanometer), ultra fine, fine and coarse particulate modes are about 34%, 37%, 63% and 30%, respectively at this traffic sampling site during the winter period.     

Deposition of atmospheric particulate PCBs in suburban site of Turkey

Dry deposition and air concentration samples were collected from July 2004 to May 2005 at a suburban site in Turkey. A water surface sampler (WSS) was used to measure directly the dry deposition flux of particulate polychlorinated biphenyls (PCBs) while a high volume air sampler (HVAS) was employed to collect air samples. Particulate PCB concentrations accounted for 15% of total PCBs (gas + particle phase) at the site. The overall particulate phase PCB flux ranged from 2 to 160 ng m^− 2 d^− 1 with an average of 46.3 ± 40.6 ng m^− 2 d^− 1. Forty one PCB congeners were targeted in the samples while twenty one congeners were found to be higher than detection limits in deposition samples. Fluxes for homolog groups ranged between 0.9 (7-CBs) and 21.0 (3-CBs) ng m^− 2 d^− 1. Measured dry deposition fluxes were lower than the ones usually reported for urban sites. Average PCB dry deposition velocity, calculated using flux values and concurrently measured atmospheric concentrations, was 1.26 ± 1.86 cm s^− 1 depended on size distribution of particles, atmospheric PCB concentrations and meteorological conditions.     

Chemical compositions of wet precipitation and anthropogenic influences at a developing urban site in southeastern China

A comprehensive study on the chemical compositions of wet precipitation was carried out from January 2004 to December 2004 in Jinhua, southeastern China's Zhejiang Province. All samples were analyzed for pH, electrical conductivity and major ions (F⁻, Cl⁻, NO₃⁻, SO₄²⁻, K⁺, Na⁺, Ca²⁺, Mg²⁺ and NH₄⁺). The rainwater was typically acidic with a volume-weighted mean pH of 4.54, which ranged from 3.64 to 6.76. SO₄²⁻ and NO₃⁻ were the main anions, while NH₄⁺ and Ca²⁺ were the main cations. The concentrations of these major ions were generally higher compared to those reported in other parts of the world, but much lower than those in northern China.Wet deposition fluxes of major ions showed pronounced seasonal variations with maximum in spring and minimum in autumn. Significant correlations were found in soil-derived species among Ca²⁺, Mg²⁺ and K⁺ and sea-salt species between Na⁺ and Cl⁻. Other relatively good correlations were also observed between Ca²⁺ and SO₄^2-, Mg²⁺ and SO₄^2-, Mg²⁺ and NO₃⁻, Mg²⁺ and Cl⁻. Principal component analysis was also performed on individual precipitation to find possible sources of the major ionic species. Varimax rotated four components accounting for 85.9% of the total variance, and were interpreted as acid and alkaline pollutants, sea spray and mixed source, soil and acid/neutralization. Calculation of enrichment factors for rainwater components relative to soil and seawater indicated that Ca²⁺ and K⁺ mainly originated from the terrestrial source, and SO₄^2- and NO₃⁻ were mostly attributed for the anthropogenic activities in the study area. In general, the results suggested that precipitation chemistry is strongly influenced by anthropogenic sources rather than natural and marine sources. The pollutants in rainwater were mainly derived from long distance transport, local industry and traffic sources.     

Determination of nitrogen dioxide in ambient air employing diffuse reflectance Fourier transform infrared spectroscopy

This paper presents the development of a simple and precise analytical method for the determination of nitrogen dioxide in ambient air. In this method nitrogen dioxide is determined in the form of nitrite. The determination of nitrogen dioxide needs no reagents except for a solution of sodium hydroxide mixed with sodium arsenite (NaOH–Na₂As₂O₃) which is used as an absorbing reagent for trapping the nitrogen dioxide from the atmosphere in the form of nitrite, i.e., a prior analysis step. The determination of submicrogram levels of nitrogen dioxide is based on the selection of a strong and sharp quantitative analytical peak at 1380 cm^− 1 using diffuse reflectance infrared spectroscopy (DRS-FTIR). The limit of detection (LOD) and the limit of quantification of the method are found to be 0.008 μg g^− 1 NO₂⁻ and 0.05 μg g^− 1 NO₂⁻, respectively. The precision in terms of standard deviation and relative standard deviation value at a level of 2 μg NO₂⁻ / 0.1 g KBr for n = 10 is found to be 0.036 μg NO₂⁻ and 1.8%, respectively. The relative standard deviation (n = 10) for the determination of nitrogen dioxide in ambient air was observed to be in the range 2.6–3.8%. The method proposed is time-saving and eliminates the slow and cumbersome steps of pH maintenance of the reaction mixture and color formation of the EPA recommended spectrophotometric and other methods for quantitative determination of nitrogen dioxide.     

Chemical characteristics of wet precipitation at an urban site of Guangzhou, South China

The pH variation and chemical characteristics of rainwater were investigated from January 2006 to December 2006 at an urban site of Guangzhou, South China. The rainwater was typically acidic with a volume-weighted mean pH value of 4.49, which ranged from 3.52 to 6.28. The volume-weighted mean equivalent concentration of components followed the order: SO₄²⁻ > Ca²⁺ > Cl⁻ > NH₄⁺ > Na⁺ > NO₃⁻ > K⁺ > Mg²⁺ > F⁻, indicating that SO₄²⁻, Cl⁻ and NO₃⁻ were the main anions, while Ca²⁺ and NH₄⁺, were the main cations. Ca²⁺ and NH₄⁺ were major neutralization constituents of the precipitation. Furthermore, correlation analysis and principal component analysis method were performed to identify possible common sources of major ions. Sources of the major ions were assessed based on enrichment factor method.     

Asian Dust effects on Total Suspended Particulate (TSP) compositions at Gosan in Jeju Island, Korea

The compositions of TSP between AD and NAD storm periods were compared to study their long-term variations and chemical characteristics. TSP samples were collected at Gosan site in Jeju Island of Korea from February to May of 1992–2004. The major ionic and elemental species of TSP aerosols were analyzed. During AD periods, the concentrations of crust components (nss-Ca²⁺, Al, Fe, Ca, Mg, Ba, Sr, Ti) increased remarkably, and the concentrations of anthropogenic components (nss-SO₄²⁻, NO₃⁻, S, Zn, Pb, Cr, Ni, Cd), with the exception of NH₄⁺, increased weakly. The concentration ratios of all major components between AD and NAD periods showed ranges from 1.2 to 8.5, except for NH₄⁺. The slope of the linear regression indicated that the contribution of CO₃²⁻ may have comprised up to 17% of the total anions. Our results suggested that the AD storm greatly influenced TSP compositions. Linear regression analyses indicated that NH₄⁺ was not correlated with NO₃⁻, but highly correlated with nss-SO₄²⁻ during both periods. The nss-SO₄²⁻ was also correlated with NH₄⁺, K⁺, nss-Mg²⁺, and nss-Ca²⁺ during both periods. Interestingly, NO₃⁻ was associated with nss-Ca²⁺ and nss-Mg²⁺ during AD periods. Of the metal elements, Fe, Ca, Mg, Ti, Mn, Ba, Sr, V, and Co were highly correlated with Al during both periods, signifying that these metals were mostly originated from soils.     

Biogenic emissions from Pinus halepensis: a typical species of the Mediterranean area

Volatile organic compounds (VOCs) emissions by vegetation present in the Mediterranean area are not well known. They may contribute with anthropogenic VOC emissions to the tropospheric ozone formation that reaches important level in the European Mediterranean region. The present work, carried out as part of the European ESCOMPTE project «fiEld experimentS to COnstrain Models of atmospheric Pollution and Transport of Emissions», adds a new contribution to the inventory of the main natural hydrocarbons sources likely to participate in the ozone production. The corresponding measurement campaign was conducted in La Barben, a site close to Marseilles (France), with the aim to quantify the terpenic emission pattern and the behaviour of Pinus halepensis, an important Mediterranean species slightly studied.The determination of biogenic emissions from P. halepensis was done by the enclosure of an intact branch in a Teflon cuvette. Main emitted monoterpenes were β trans-ocimene and linalool. The total monoterpenic emission rates thus recorded were found to reach maximum values around 30 μg g_{dry weight}⁻¹ h⁻¹. The normalized emission rates calculated at 30 °C and 1000 μmol m⁻² s⁻¹ with Guenther's algorithm was 14.76, 8.65 and 4.05 μg g_{dry weight}⁻¹ h⁻¹, respectively, for the total monoterpenes, β trans-ocimene and linalool.     

Dew water collector for potable water in Ajaccio (Corsica Island, France)

We report on the development of an inexpensive radiative condenser for collecting atmospheric vapor. Based on the experience gained using a small working model in Grenoble (France), a prototype of 10×3 m² was established in Ajaccio (Corsica, France). The condensing surface is a rectangular foil made of TiO₂ and BaSO₄ microspheres embedded in polyethylene and has an angle of 30° with respect to horizontal. The hollow part of the device, thermally isolated, faces the direction of the dominant nocturnal wind. Dew measurements were correlated with meteorological data and compared to dew condensed on a horizontal polymethylmethacrylate (PMMA, Plexiglas) reference plate. The plate served as a reference standard unit and was located nearby. Between July 22, 2000 and November 11, 2001 (478 days), there were 145 dew days for the reference plate (30%), but 214 dew days for the condenser (45%). This yield corresponds to 767 l (3.6 l, on average, per dew day). The maximum yield in the period was 11.4 l/day. Dew mass can be fitted to a simple model that predicts dew production from simple meteorological data (temperature, humidity, wind velocity, cloud cover). Chemical analyses of the water collected from the plate were performed from October 16, 1999 to July 16, 2000 and from the condenser, from July 17, 2000 to March 17, 2001. The following parameters were investigated: suspended solids, pH, concentration of SO₄²⁻, Cl⁻, K⁺, Ca²⁺ ions. Only Cl⁻ and SO₄²⁻ ions were sometimes found significant. Wind direction analyses revealed that Cl⁻ is due to the sea spray and SO₄²⁻ to the combustion of fuel by an electrical plant located in the Ajaccio Gulf. Except for a weak acidity (average pH≈6) and high concentration of suspended solids, dew water fits the requirements for potable water in France with reference to the above ions.     

An Investigation into the Ionic Chemical Composition and Mixing State of Biomass Burning Particles Recorded During TRACE-P P3B Flight#10

In this study bulk airborne aerosol composition measured by the PILS-IC (integration time of 3 min 24 s) during TRACE-P P3B Flight 10 are used to investigate the ionic chemical composition and mixing state of biomass burning particles. A biomass burning plume, roughly 3–4 days old, moderately influenced by urban pollution aerosols recorded in the Philippine Sea is investigated. Focusing on the fine particle NO₃⁻, SO₄²⁻, K⁺, NH₄⁺, and water-soluble organics, the observed correlations and nearly 1-to-1 molar ratios between K⁺ and NO₃⁻ and between NH₄⁺ and (SO₄²⁻+ inferred Organics) suggest the presence of fine-mode KNO₃, (NH₄)₂SO₄, and NH₄(Organics) aerosols. Under the assumption that these ion pairs existed, and because KNO₃ is thermodynamically less favored than K₂SO₄ in a mixture of NO₃⁻, SO₄²⁻, K⁺, NH₄⁺, and Organic anions, the measurements suggest that aerosols could be composed of biomass burning particles (KNO₃) mixed to a large degree externally with the (NH₄)₂SO₄ aerosols. A “closed-mode” thermodynamic aerosol simulation predicts that a degree of external mixing (by SO₄²⁻ mass) of 60 to 100% is necessary to achieve the observed ionic associations in terms of the existence of KNO₃. However, the degree of external mixing is most likely larger than 90%, based on both the presence of KNO₃ and the amounts of NH₄NO₃. Calculations are also shown that the aerosol mixing state significantly impacts particle growth by water condensation/evaporation. In the case of P3B Flight #10, the internal mixture is generally more hygroscopic than the external mixture. This method for estimating particle mixing state from bulk aerosol data is less definitive than single particle analysis, but because the data are quantitative, it may provide a complementary method to single particle chemical analysis.     

Size-resolved aerosol chemical concentrations at rural and urban sites in Central California, USA

Aerosol size distributions were measured with Micro Orifice Uniform Deposit Impactor (MOUDI) cascade impactors at the rural Angiola and urban Fresno Supersites in California's San Joaquin Valley during the California Regional PM₁₀/PM_2.5 Air Quality Study (CRPAQS) winter campaign from December 15, 2000 to February 3, 2001. PM_2.5 filter samples were collected concurrently at both sites with Sequential Filter Samplers (SFS). MOUDI nitrate (NO₃⁻) concentrations reached 66 μg/m³ on January 6, 2001 during the 1000–1600 PST (GMT-8) period. Pair-wise comparisons between PM_2.5 MOUDI and SFS concentrations revealed high correlations at the Angiola site (r > 0.93) but more variability (r < 0.85) at the Fresno site for NO₃⁻, sulfate (SO₄⁼), and ammonium (NH₄⁺). Correlations were higher at Fresno (r > 0.87) than at Angiola (r < 0.7) for organic carbon (OC), elemental carbon (EC), and total carbon (TC). NO₃⁻ and SO₄⁼ size distributions in Fresno were multi-modal and wider than the uni-modal distributions observed at Angiola. Geometric mean diameters (GMD) were smaller for OC and EC than for NO₃⁻ and SO₄⁼ at both sites. OC and EC were more concentrated on the lowest MOUDI stage (0.056 µm) at Angiola than at Fresno. The NO₃⁻ GMD increased from 0.97 to 1.02 µm as the NO₃⁻ concentration at Angiola increased from 43 to 66 µg m^− 3 during a PM_2.5 episode from January 4–7, 2001. There was a direct relationship between GMD and NO₃⁻ and SO₄⁼ concentrations at Angiola but no such relationships for OC or EC. This demonstrates that secondary aerosol formation increases both concentration and particle size for the rural California environment.     

Concentration and gas/particle partitioning of polychlorinated biphenyls (PCBs) at an industrial site at Bursa, Turkey

Gas and particle phase concentrations of atmospheric polychlorinated biphenyls (PCBs) were measured at an urban/industrial site in the city of Bursa, Turkey. PCB concentration levels were presented between July 2004 and May 2005. Average particle and gas phase concentrations of individual PCB congeners ranged from 0.08 (PCB-183) to 6.86 (PCB-49) pg m^− 3 and from 0.01 (PCB-209) to 47.2 (PCB-33) pg m^− 3, respectively. The mean concentration of total (gas + particle) PCBs varied between 24.27 and 666.21 pg m^− 3 with an average of 287.27 ± 174.80 pg m^− 3. PCB concentrations at the sampling site were higher than the concentrations reported at non-urban sites. PCBs partitioned between gas and particle phases and the partitioning was examined according to different approaches such as logK_p–logP_L^o, logK_p–logK_OA and the Junge–Pankow model. In order to present possible interactions, a correlation matrix based on PCB congeners and meteorological parameters was constructed. Application of the Clausius–Clapeyron equation yielded a low slope value indicating possible emissions from local and regional sources originating mainly from urban/industrial areas, landfill and waste incineration plant. Then, likely dry deposition fluxes were estimated depending on reported dry deposition velocity and atmospheric concentration values.     

Microphysical and optical features of polluted cooling tower clouds

In November 1993 an airborne field study was performed in order to investigate the microphysical and radiative properties of cooling tower water clouds initiated by water vapour emissions and polluted by the exhaust from coal-fired power plants. The number-median diameter of the droplet size distributions of these artificial clouds was in the range of 13 μm. The concentration of smaller droplets (diameters d_D < 10 μm) increased with height and horizontal distance from the cooling towers. Close to the cooling towers, bimodal spectra were found with a second mode at 19 μm. The liquid water content (LWC) ranged between 2 and 5 g/m³ and effective droplet radii (R_e) between 6 and 9 μm were measured. LWC and R_e decreased with altitude, whereas the droplet concentration (N_D) remained approximately constant (about 2000 cm⁻³ ). An enrichment of interstitial aerosol particles with particle diameters (d_p) smaller 0.2 μm compared to the power plant plume in the vicinity of the clouds was observed. Particle activation for d_m > 0.3 μm. was evident, especially in cooling tower clouds further apart and separated from their sources. Furthermore, radiation measurements were performed, which revealed differences in the vertical profiles of downwelling solar and UV radiation flux densities inside the clouds.The effective droplet radius R_e was parameterized in terms of LWC and N_D using equations known from literature. The close agreement between measured and parameterized Re indicates a similar coupling of R_e, LWC and N_D as in natural clouds.By means of Mie calculations, volume scattering coefficients and asymmetry factors are derived for both the cloud droplets and the aerosol particles. For the cloud droplets, the optical parameters were described by parameterizations from the literature. The results show, that the link between radiative and microphysical properties of natural clouds is not changed by the extreme pollution of the artificial clouds.