Anthropogenic Calcium Particles Observed in Beijing and Qingdao, China

Analysis of individual particles collected at Beijing in northern China revealed that particles abundant in calcium (Ca) always constituted a large fraction of mineral particles in the urban atmosphere. The particles were characterized by cubic morphologies. The major mineral element in the particles was Ca and few or no other mineral elements were detected. A large number of the particles were in the range of diameter <1 μm, where common natural mineral particles were rarely detected. The contribution of the Ca particles to the volume of total mineral particles greatly exceeded that of other mineral particles during non-dust-storm periods and was comparable to that during dust-storm periods. Reagent film tests showed that particulate sulfate and nitrate formation on the Ca particles was similar to that on common mineral particles. These results indicate that a large portion of Ca in the atmospheric particulate matter in Beijing was from anthropogenic sources rather than from natural sources, and the anthropogenic Ca particles acted as a significant medium for the formation of sulfate and nitrate. Similar particles were also detected at Qingdao, a coastal city in northern China. Data of a dust storm event showed that Ca-abundant particles from East China arrived there and moved out of the continent, similarly to Asian dust storm particles, suggesting possible contributions of anthropogenic Ca even in Asian dust storm samples in the downstream areas. Therefore, Ca may not be a good indicator of Asian dust from natural sources. However, the Ca particles, due to their unique shapes and elemental compositions, may provide an indicator for the atmospheric dispersion of anthropogenic particulate matters in East Asia.     

Characteristics of air pollution in Beijing during sand-dust storm periods

In the Beijing area, March and April have the highest frequency of sand-dust weather. Floating dust, blowing sand, and dust storms, primarily from Mongolia, account for 71%, 20%, and 9% of sand-dust weather, respectively. Ambient air monitoring and analysis of recent meteorological data from Beijing sand-dust storm periods revealed that PM₁₀ mass concentrations during dust storm events remained at 1500 μg m⁻³, which is five to ten times higher than during non-dust storm periods, for fourteen hours on both April 6 and 25, 2000. During the same period, the concentrations in urban areas were comparable to those in suburban areas, while the concentrations of gaseous pollutants, such as SO₂, NO _x , NO₂, and O₃, remained at low levels, owing to strong winds. Furthermore, during sand-dust storm periods, aerosols were created that consisted not only of many coarse particles, but also of a large quantity of fine particles. The PM_2.5 concentration was approximately 230 μg m⁻³, accounting for 28% of the total PM₁₀ mass concentration. Crustal elements accounted for 60–70% of the chemical composition of PM_2.5, and sulfate and nitrate for much less, unlike the chemical composition of PM_2.5 on pollution days, which was primarily composed of sulfates, nitrates, and organic material. Although the very large particle specific surface area provided by dust storms would normally be conducive to heterogeneous reactions, the conversion rate from SO₂ to SO₄ ²⁻ was very low, because the relative humidity, less than 30%, was not high enough.     

Characterization of Dust Storms to Hong Kong in April 1998

In April 1998, two intense dust storms were generated in CentralAsia and transported eastward across East Asia (15 and 19 April). This article presents the chemical characterization ofHong Kong (HK) aerosols during the dust storms. During the 15 Aprildust storm, hourly respiratory suspended particles (RSP)(particle diameter smaller than 10 m) concentrationsmonitored at 7 sites in Hong Kong reached the peak valuessynchronously between 9 and 11 a.m. on 17 April, in which thehighest concentration was 267 g m^-3. Analysis ofthe RSP samples showed that concentrations of crustalelements (Ba, Ca, Cd, Cr, Fe, Mg, K⁺) and anthropogenicspecies (As, Ni, Pb, Zn, NH₄ ⁺, NO₃ ^-,SO₄ ^2- and total carbon) were substantiallyenhanced. Enhancement of these species was more than afactor of 2 to 14 relative to the non dust period. The totalcarbon content was high, at 59 g m^-3 (notincluding carbonate), and the enrichment factors of Asand Pb on 17 April were 122 and 117, respectively. Thisimplied that anthropogenic materials together with mineraldust were transported to HK from Mainland China. Based onmaterial balance calculations, mineral dust contributed41% to the observed RSP mass on 17 April, which was 2 times thatof the nondust sample (22%). From the 5-day backwardtrajectory analysis, this storm was transported directlyfrom Northwest China to HK. However, there was nocorresponding observation for the 19 April dust stormaerosol. Consequently, 15 April storm had stronger impact onHK's atmosphere than 19 April storm. Compared to the HK AirQuality Objective, 15 April dust storm did not cause seriousair pollution in HK.     

Monitoring Studies of Precipitation and Cap Cloud Chemistry at Holme Moss in the Southern Pennines

Weekly collections of samples of precipitation and hill cloudwater have been made at Holme Moss (530 m.a.s.l.) in the southernPennines covering a six-year period (1994–1999). In addition continuous meteorological measurements have been conducted at thesite for a five year period (1995–1999). The concentrations of major ions in the samples have been determined by ion chromatography. Analysis of ion concentrations as a function ofwind direction reveals that the ions with anthropogenic sources (SO₄ ^–, NO₃ ^–, NH₄ ⁺, H⁺) exhibit higher concentrations during easterly wind directions whilst the ions with predominantly marine origins (Na⁺, Cl^–, Ca⁺⁺, Mg⁺⁺, K⁺) have concentrations thatare not significantly dependant on wind direction. Precipitation and cloud deposition are strongly correlated to south-westerly wind directions with a secondary peak occurring for north-easterly directions. Fifty nine per cent of ion deposition by rain was found to occur during wind from the SSW to W sector.The average concentrations of ions in cloud water were found tobe much higher than those in rain (by factors of between 2.5 and4.2). It is thought that the high precipitation and annual deposition of ions by precipitation at Holme Moss is due in partto the enrichment of ion concentrations in precipitation by thescavenging of more concentrated cap cloud droplets (the `seeder-feeder effect'). Comparison with data from a nearby lower level site shows encouraging agreement with the scheme currently used in the U.K. deposition mapping procedure to incorporate the influence of orography on deposition by precipitation.     

Study of Trace and Heavy Metals in Rural and Urban Aerosols of Uludağ and Bursa (Turkey)

The concentrations of heavy, trace elements and major ions measuredin the Uluda and Bursa aerosols were investigated to assess size distributions, spatial and temporal variability, sources and source regions affecting the composition of aerosols in Uluda and Bursa. A total of 81 samples were collected in two sites, one in Bursa city and another in the Uluda Mountain during two sampling campaigns. Daily samples were collected using a high volume sampler on Whatman 41 cellulose filters in Uluda, while three days interval samples were collected in Bursa using an automatic dichotomous sampler on PTFE Teflon filters. Samples were analysed for 15 trace and heavy metals (Al, Fe, Ba, Na, Mg, K, Mn, Ca, Cu), (V, Pb, Cd, Cr, Ni, Zn), and 4 major ions (SO₄ ^2-, NO₃ ^-, Cl^-), (NH₄ ⁺) using ICP-AES, GFAAS, HPLC and UV/VIS Spectrophotometer,respectively. In general, concentrations of the metals measured inUluda aerosols were lower than those in Bursa. The concentrations of crustal elements were higher in summer than winter, while anthropogenic elements had higher concentrations in winter than summer. Most of the mass of crustal elements was concentrated in the coarse mode while the mass of the heavy metals was concentrated in the fine mode. Factor analysis revealed four factors with sources including crustal, industrial and combustion. Back trajectory calculations were used to determine long range contributions. These calculations showed that contributions were mostly from European countries, former Soviet Union countries, Black Sea and North Africa.     

Numerical Simulation of Synoptic Condition on a Severe Sand Dust Storm

By using observational data and MM5, an observational analysisand numerical study was conducted on the synoptic condition of a severe dust storm that was caused by a Mongolian cyclone whichoccurred from 6 to 8 April 2001. Results illustrated thatthe cyclogenesis was due to the isentropic potential vorticity (IPV) advection in the upper troposphere and the terrain modifiedbaroclinicity in the mid-lower troposphere. The Altai-Sayan complex of mountains blocked the lower level cold air and made the isentropic surface sharply steep. When the air slid down along the isentropic surface the increasing of baroclinicity anddecreasing of stability blew up the vertical vorticity development.The formation of the dust storm was a result of a cyclonic cold front passing across the area. The occurrence of this dust stormwas closely related to the strong surface wind, which was accompanied by a cold front passing, rather than the cyclogenesis, itself. Hence, the reason for the pre-front dust storm formulation was the formation of heating convection. Reasons behind the formation of a black storm (visibilitylower than 50 m), which occurred in the mid-north part ofInner Mongolia, lay in several aspects. Firstly, in thisarea the surface wind was strong, a direct result of thedownward transport in mid-lower troposphere. Secondly,the cold front passed over the effected area near sunsetso the air obtained much more surface heating to form adeeper mixed layer (ML). Thirdly, cooperation between thelower level wind and the terrain made the atmosphere inthis area and acquired the maximum advective contributionnecessary to form a deep post-front ML. The sensitivityexperiment revealed that surface heat flux was important to the frontal lifting. In addition, the forcing of surface heating wasalso seen as the primary forcing mechanism of frontogenesis. Meanwhile, removal of the surface heat flux made the atmosphericstratification became stable and the pre-storm ML very shallow,which weakened the strength of the dust storm.     

Modeling of Combined Aerosol and Photooxidant Processes in the Mediterranean Area

The combined UAM-AERO/RAMS modeling system has been applied to study the dynamics of photochemical gaseous species and particulate matter processes in the eastern Mediterranean area between the Greek mainland and the island of Crete. In particular, the modeling system is applied to simulate atmospheric conditions for two periods, i.e., 13-16 July 2000 and 26-30 July 2000. The spatial and temporal distributions of both gaseous and particulate matter pollutants have been extensively studied together with the identification of major emission sources in the area. New pre-processors were developed for the UAM-AERO model for evaluating detailed emission inventories for biogenic compounds, resuspended dust and sea salt. Comparison of the modeling results with measured data was performed and satisfactory agreement was found for a number of gaseous species. However, the model underestimates the PM₁₀ measured concentrations during summer. This is mainly due to the considerable underestimation of particulate matter emissions and in particular dust resuspension, the effect of forest fire emissions and the contribution of Saharan dust episodes.     

Feature of Dust Particles in the Spring Free Troposphere over Dunhuang in Northwestern China: Electron Microscopic Experiments on Individual Particles Collected with a Balloon-borne Impactor

Free tropospheric aerosol particles were collected using a balloon-borne particle impactor in August of 2002 and March of 2003 at Dunhuang in northwestern China (40°00′N, 94°30′E), and the morphology and elemental composition of the aerosol particles were analyzed in order to understand the mixing state of coarse dust particles (diameter >1 μm) over the desert areas in the Asian continent in spring. Electron microscopic experiments on the particles revealed that dust particles were major constituents of coarse mode particles in the free troposphere over the Taklamakan Desert in spring and summer. Si-rich or Ca-rich particles are major components of dust particles collected in the free troposphere over dunhuang and the values of [number of Ca-rich particles]/[number of Si-rich particles] differs markedly between spring and summer, being about 0.3 in the spring of 2003 and about 1.0 in the summer of 2002 at heights 3–5 km above sea level. It is likely that the condition of the ground surface and the strength of vertical mixing in source areas of Asian dust are potential factors causing the difference in the chemical types of dust particles. Comparison of the elemental compositions of these particles with those of particles collected over Japan strongly suggests that these particles were chemically modified during their long-range transport in the free troposphere. Analysis of wind systems shows that both the predominating westerly wind in the free troposphere and the surface wind strongly controlled by the geographical structure of the Tarim Basin are important in the long-range transport of KOSA particles originating in the Taklamakan Desert.     

Natural and Anthropogenic Changes in The Chemistry of Six UK Mountain Lakes, 1988 to 2000

Trends have been analysed for 12 years ofchemical data from six mountain lakes in the UK AcidWaters Monitoring Network (AWMN). With minimal localanthropogenic impacts, these sites offer the bestavailable opportunity for clear identification of surfacewater chemical response to external factors, whethernatural or anthropogenic. Results indicate that naturalclimatic variations have had a major impact on lakechemistry, through fluctuations in (i) intensity ofstorms, which cause dilution of weathering-derived basecations, and/or displacement of hydrogen and aluminiumions on soil exchange sites by deposited marine basecations; and (ii) winter temperature, which is thought tobe inversely related to spring nitrate (NO₃) maxima.Both climatic factors can be linked to the North AtlanticOscillation. For the first decade of AWMN monitoringthese natural `confounding factors' to a significantextent obscured any recovery from acidification due todeclining anthropogenic sulphur deposition. However, theadditional data presented here provide strengtheningevidence for chemical recovery at a number of sites, atwhich decreases in sulphate (SO₄), acidity andlabile aluminium can now be identified. It is believedthat changes at these sensitive mountain lake sites mayherald more widespread recovery in UK surface waters aspollutant emissions decline further. However, largeincreases in dissolved organic carbon, and hence inorganic acidity, may have partially offset reductions inmineral acidity. The cause of these increases remainsuncertain, but may be linked to climatic change.     

Speciation and Seasonal Variations of Dissolved Inorganic Arsenic in Jiaozhou Bay,North China

The distributions and biogeochemical cycles of arsenic in the aquatic environment have captured the interest of geochemists due to arsenic’s multiple chemical forms, the toxicity of certain arsenic species and large anthropogenic input. Seasonal variations in the dissolved inorganic arsenic concentration and speciation in Jiaozhou Bay, which is located on the west coast of the Yellow Sea in northern China, are presented here. Three cruises were carried out in Jiaozhou Bay under varying tidal regimes, one at neap tide and one at spring tide in August and one at spring tide in October of 2001. In addition to the transect surveys, the main sources of dissolved inorganic arsenate and arsenite in Jiaozhou Bay, including riverine input from five major tributary rivers, atmospheric dry and wet depositions, and groundwater and wastewater input, were collected in different seasons to estimate arsenic transport through different sources. The mean concentrations of total dissolved inorganic arsenic (TDIAs, As (V+III)) in Jiaozhou Bay were statistically comparable between summer and autumn, with higher concentrations at the northwest and northeast parts of the bay, reflecting human activities. The As (III)/TDIAs ratio ranged between 0.045 and 0.68, with an average of 0.16, implying that arsenate was the dominating species in Jiaozhou Bay. A preliminary box model was established to estimate the water-mass balance and arsenic budgets for Jiaozhou Bay, which demonstrated that river inputs and atmospheric depositions were the main sources of arsenic into Jiaozhou Bay. The concentrations of dissolved inorganic arsenic in Jiaozhou Bay have decreased in the last two decades. Compared with other areas in the world, the concentration of arsenic in Jiaozhou Bay remains at the natural level and this region can be characterized as a less disturbed area.     

Discriminate Analysis for Dust Storm Prediction in the Gobi and Steppe Regions in Mongolia

A discriminate analysis method for probability forecast of dust storms in Mongolia has been developed. The prediction method uses data recorded at 23 meteorological stations in the Gobi and steppe regions of Mongolia, including surface air pressure and geo-potential height at the 500-hPa level on grid points, and weather maps from 1975 to 1990. Weather elements such as air temperature, pressure, geo-potential height etc, which influence the formation of dust storms, are prepared as predictors. To select the most informative/important predictors (variables), we used a mean correlation matrix of variables together with the Mahalonobis distance, and correlation coefficients between dust storms and predictors with an orthogonalization for removing correlated predictors. The most informative predictors for dust storm prediction are intensities of surface cyclones and migratory anticyclones, passage of cold fronts, the horizontal gradients of the surface air pressure in the cold frontal zone, cyclonic circulations from the ground surface up to the 500-hPa level, the geo-potential height at 500-hPa level and its temporal changes. Selected predictors are used in discriminate analysis for formulating dust storm prediction equations. Sandstorm data have been classified into three classes, viz., strong, moderate and weak dust storms, depending on their intensities, durations and areas covered. Predictions of the probabilities of dust storm occurrence use the prediction equations for each class. The prediction is made from 12 hours to 36 hours. Verification of the probability forecasts of dust storms is also shown. The accuracy of forecasts is 72.2–79.9% with the data used for developing equations (dependent variables), in contrast to 67.1–72.0% with unrelated data for deriving equations (independent variables).     

Aerosol Particle Processing and Removal by Fogs: Observations in Chemically Heterogeneous Central California Radiation Fogs

Fog composition and deposition fluxes of fog waterand fog solutes were measured in six radiation fogevents in San Joaquin Valley, California duringwinter 1998/1999. Measurements made at 2 hrintervals with 0.30 m² and 0.06 m² Teflondeposition plates yielded excellent reproducibility(relative standard deviations of 3.8–6.0%) forwater, nitrate, sulfate and ammonium. Water fluxesmeasured at 5 min intervals with a recordingbalance agreed well with the deposition platemeasurements before 8:00 AM. After 8:00 AMevaporation proved problematic. The averagedeposition velocity from the study for fog nitrate(3.8 cm s^-1) was less than those for fogsulfate (5.1 cm s^-1) and ammonium (6.7 cms^-1). All three species generally exhibitedsmaller deposition velocities than fog water. Thespecies dependent trend in deposition velocitieswas consistent with preferential enrichment ofthese species in small fog drops (nitrate > sulfate> ammonium).     

A Comparison of Loch Chemistry from 1955 and 1999 in the Cairngorms,N.E. Scotland

The Cairngorms in north-east Scotland is remote from pollutant sources although it currently receives ca. 10 kg ha¹ yr¹ S and ca. 11 kg ha¹ yr¹ N deposition from the atmosphere.In 1955, 15 lochs (lakes) at a range of altitudes were sampled and analysed for major ion concentrations. A new survey of these and an additional 23 lochs and their catchment soils was conducted in 1999 to determine the impact of acid deposition, and the changes in loch chemistry since the 1955 survey. The bedrock geology of this region has a strong influence on the loch chemistry. Surface waters were generally more acidic in high altitude areas due to predominantly poorly buffered, thin alpine soils developed on granitic parent material (mean acid neutralising capacity (ANC) for 23 lochs = 30 eq L¹). At lower altitudes where the geology is dominated by Dalradian metamorphic rocks surface waters are comparatively base rich and have higher ANC (mean ANC for 15 lochs = 157 eq L¹). Surface water nitrate concentrations show a negative relationship with soil C:N status, in that higher nitrate only occurs at low soil C:N ratios. A comparison of data for 1955 and 1999 shows that sulphate concentrations are significantly lower (67.8 and 47.5 eq L¹, respectively), and pH has improved (pH 5.6 and 5.9) in response to decreased S deposition since the mid 1970s. However, mean nitrate concentrations were found to increase from 2.48 >eq L¹ in 1955 to 5.65 eq L¹ in 1999. Differences in the sampling and laboratory methods from 1955 and 1999 are acknowledged in the interpretation of data.     

Identification of PM10 Sources in a Mediterranean Island

Due to the dry Mediterranean climate in Cyprus, particulate matter is resuspended from soils and other surfaces. From November 2002 to August 2003, gravimetric PM₁₀ measurements were carried out at three characteristic sites (traffic, residential and rural). A significant seasonal trend with high winter concentrations was observed at the traffic site. Special events, e.g. long-range transport of Sahara dust storms, were recorded over traffic, residential and rural areas in the order of six to eight events per year, with a major frequency in summer and spring periods. This contributes to the increase of 24-h EU limit value exceedances for PM₁₀ at the three investigated sites. The origin of the PM₁₀ load was determined by enrichment factors based on analyses of the local soil deposition at the investigated sites. Furthermore, positive matrix factorisation modelling was applied to find the sources of PM₁₀. Results indicate that the major emission sources affecting the PM₁₀ load were mineral soil, sea salt, road dust, oil combustion, secondary pollutants and gasoline vehicles. The natural contribution (local mineral soil and sea salt) at the three sites was in the range of 7–9 μg m^?3 in PM₁₀. Besides the Sahara dust storms and natural background concentrations, the vehicular pollution was found as the largest contributor (12–14 μg m^?3) to PM₁₀ load at the traffic site.     

Comparison of PM2.5 and PM10 in A Suburban Area in Korea During April, 2003

Airborne particulate matter (PM) concentrations were measured in Iksan, a suburban area in South Korea during April, 2003. PM_2.5 (particles with an aerodynamic diameter less than 2.5 μm) and PM₁₀ (particles with an aerodynamic diameter less than 10 μm) samples were collected, and the chemical characteristics of particles were examined for diurnal patterns, yellow dust/rainfall influences, and scavenging effects. Average concentrations of PM_2.5 and PM₁₀ mass measured were 37.3 ± 16.2 μg m⁻³ and 60.8 ± 29.5 μg m⁻³, respectively. The sum of ionic chemical species concentrations for PM_2.5 and PM₁₀ was 16.9 ± 7.3 and 23.1 ± 10.1 μg/m³, respectively. A significant reduction in PM mass concentrations during rainfall days was observed for coarse mode (PM_{2.5 − 10}) particles, but less reduction was found for fine (PM_2.5) mass concentration. SO₄ ²⁻, NH₄ ⁺, and K⁺ predominated in fine particulate mode, NO₃ ⁻ and Cl⁻ predominated in fine particle mode and coarse particle mode, but Na⁺, Mg²⁺, and Ca²⁺ mostly existed in coarse mode. The high concentration of ammonium due to local emissions and long-range transport neutralized sulfate and nitrate to ammonium sulfate and ammonium nitrate, which were major forms of airborne PM in Iksan. Average mass concentrations of PM₁₀ in daytime and at night were 57.6 and 70.0 μg m⁻³, and those of PM_2.5 were 35.4 and 42.5 μg m⁻³, respectively. NO₃ ⁻ and Cl⁻ in both PM_2.5 and PM₁₀ were about double at night than in the daytime, while the rest of the chemical species were equal or a little higher at night than in the daytime. The results suggest the formation of ammonium nitrate and chloride when high ammonia concentration and low air temperature are allowed. Backward air trajectory analyses showed that air masses arriving at the site during yellow dust period were transported from arid Chinese regions, which resulted in high concentrations of airborne PM mass concentrations. In the meantime, air mass trajectories during a rainfall period were mostly from the Pacific Ocean or the East China Sea, along with a relatively low PM concentration.     

Local Circulation with Aeolian Dust on the Slopes and Foot Areas of the Tianshan and Kunlun Mountains around the Taklimakan Desert, China

Four automatic weather stations (AWS) were installed on the slopes and foot areas of the Tianshan and Kunlun Mountains along a longitude of 80 degrees east: (1) Taglak 2400 m a.s.l., (2) Aksu 1000 m, (3) Kartash 2800 m, and (4) Qira 1700 m. These two slopes face the Taklimakan Desert. Tagliak lies on the southern slope of Tianshan, and Kartash on the northern slope of Kunlun. The meteorological characteristics of the mountainous regions were investigated using surface data obtained during an intensive observation period (IOP) in spring 2002. It was found that visibility on the slopes decreases in the daytime, and there is no relationship between visibility and wind speed in the mountainous areas. Two snow layers containing dust particles were observed in the snow cover in Taglak during the IOP in spring 2003. These results suggest that a warm air parcel containing aeolian dust climbs over the slopes of the mountainous areas, and dust particles in the mountainous areas are transported from the foot areas.     

What Anthropogenic Radionuclides (90Sr and 137Cs in Atmospheric Deposition, Surface Soils and Aeolian Dusts Suggest for Dust Transport over Japan

Currently, atmospheric anthropogenic radionuclides (particulate) are controlled by suspension of the surface dust containing those radionuclides (resuspension). We have found, therefore, that such radionuclides can be used as tracers of the surface dust suspension, transport and its subsequent deposition in distant areas. The ¹³⁷Cs/⁹⁰Sr activity ratios in the atmospheric deposition, without the direct influence of nuclear tests and accidents, at the Meteorological Research Institute (MRI, Tsukuba, Japan) during the 1990s were fairly low (average: 2.1). This value is not in agreement with the ratios in Japanese surface soils (range of averages: 4–7), which had been considered as the primary source of the deposited dust. This suggests that the current atmospheric dust deposition in Japan is a mixture of local and remote components. The remote component could be an aeolian dust that has been transported long distances from arid areas. The major component is most likely to be Asian dust. It was further hypothesized that other remote source may exist beyond the Asian domain, based on accumulated observations and model results. To obtain more information about the dust transport, Sahara dust deposited in Monaco in 2002 and a suspended dust collected in the Taklamakan area in 2001 were analyzed for ⁹⁰Sr and ¹³⁷Cs. The Taklamakan dust exhibited a ¹³⁷Cs/⁹⁰Sr ratio of about 4, which is within the range of atmospheric deposition observed at the MRI, while the Sahara dust exhibited a higher ¹³⁷Cs/⁹⁰Sr ratio (about 13). Although the present Sahara datum was negative for our hypothesis of ‘hyper-range transport’, the seasonal change of the ¹³⁷Cs/⁹⁰Sr ratio in the atmospheric deposition observed at the MRI requires an aeolian dust source having a low ¹³⁷Cs/⁹⁰Sr ratio, other than Asian dust.     

Evaluation of Air Quality over the Black Sea: Major Ionic Composition of Rainwater

This article attempts to put the light on the air quality of the Black Sea region of Turkey. In addition to that, it endeavors to locate the possible sources of the different pollutants at local, regional and long range transported scales. About 196 rainwater samples were collected over the Black Sea region of Amasra between 1995 and 1999, and analyzed for major ions and trace elements using spectrophotometric techniques. Andersen wet only rain samples were used to collect rain events, where the rain sample was filtered inline using 0.45 m cellulose acetate filters. Major anions (SO₄ ^2-, NO₃ ^- and Cl^-) were determined using ion chromatography, whereas metals (Ca, Mg, Al, Fe, Na, K), werequantified using ICP-AES. This study shows that, the Black Sea region receives different amounts and types of anthropogenic pollutants via long-range transport according to trajectory models. Although the pH of rain water is not considered acidic (pH = 5.21) yet the neutralizing species are lower than other sites around Europe.     

Temporal Trends of Non-sea Salt Sulfate and Nitrate in Wet Deposition in Japan

Temporal trends of non-sea salt (nss-) sulfate and nitrate were analyzed from nationwide precipitation chemistry measurements provided by the Ministry of the Environment (MOE) for the 1988–2002 fiscal years (April–March). The concentrations and deposition of nss-sulfate were found to be decreasing, and those of nitrate were stable or slightly increasing at most sites. These deposition trends were discussed from the viewpoint of emissions of SO₂ and NO_X during the period of interest. Because monitoring techniques have changed in the number of active sites, samplers, and analytical methods during the operation period, the median of all annual depositions measured in Japan in a specific year was selected as the annual representative. The contribution of specific emission sources was also calculated for 1990 on the basis of the nss-sulfate and nitrate deposition in Japan obtained with a model simulation in which the model did not include volcanic emissions from Mt. Oyama, Miyakejima Island, which began to erupt suddenly and violently in 2000. For nss-sulfate, the calculated deposition agrees well with the intensity and trends of the median up to 1999. After 2000, a higher deposition than calculated in the preceding years was evident, which is attributable to the volcanic SO₂ from Mt. Oyama. For nitrate, both the calculated and observed depositions were slightly increasing; however, the calculation was found to exceed the observation.     

The effect of dust emissions from open storage piles to particle ambient concentration and human exposure

The current study focus on the determination of dust emissions from piles in open storage yards of a municipal solid waste (MSW) composting site and the subsequent atmospheric dust dispersion. The ISC3-ST (Industrial Source Complex Version 3 – Short Term) model was used for the evaluation of the PM₁₀ ambient concentrations associated with the dispersion of MSW compost dust emissions in air. Dust emission rates were calculated using the United States Environmental Protection Agency proposed dust resuspension formulation from open storage piles using local meteorological data. The dispersion modelling results on the spatial distribution of PM₁₀ source depletion showed that the maximum concentrations were observed at a distance 25–75 m downwind of the piles in the prevailing wind direction. Sensitivity calculations were performed also to reveal the effect of the compost pile height, the friction velocity and the receptor height on the ambient PM₁₀ concentration. It was observed that PM₁₀ concentrations (downwind in the prevailing wind direction) increased with increasing the friction velocity, increasing the pile height (for distances greater than 125 m from the source) and decreasing the receptor height (for distances greater than 125 m from the source). Furthermore, the results of ISC3-ST were analysed with the ExDoM (Exposure Dose Model) human exposure model. The ExDoM is a model for calculating the human exposure and the deposition dose, clearance, and finally retention of aerosol particles in the human respiratory tract (RT). PM₁₀ concentration at the composting site was calculated as the sum of the concentration from compost pile dust resuspension and the background concentration. It was found that the exposure to PM₁₀ and deposited lung dose for an adult Caucasian male who is not working at the composting site is less by 20–74% and 29–84%, respectively, compared to those for a worker exposed to PM concentrations at the composting site.