PM10 and PM2.5 Levels in the Eastern Mediterranean (Akrotiri Research Station, Crete, Greece)

Particulate matter measurements (PM₁₀, PM_2.5) using a beta radiation attenuation monitor were performed at the Akrotiri research station (May 2003–March 2006) on the island of Crete (Greece). The mean PM₁₀ concentration during the measuring period (05/02/03–03/09/04) was equal to 35.0?±?17.7 μg/m³ whereas the mean PM_2.5 concentration (03/10/04–04/02/06) was equal to 25.4?±?16.5 μg/m³. The aerosol concentration at the Akrotiri station shows a large variability during the year. Mean concentrations of particulate matter undergo a seasonal change characterised by higher concentrations during summer [PM₁₀, 38.7?±?10.8 μg/m³ (2003); PM_2.5, 27.9?±?8.7 μg/m³ (2004) and 27.8?±?9.7 μg/m³ (2005)] and lower concentrations during winter [PM₁₀, 28.7?±?22.5 μg/m³ (2003/2004); PM_2.5, 21.0?±?13.0 μg/m³ (2004/2005) and 21.4?±?21.9 μg/m³ (2005/2006)]. Comparative measurements of the PM₁₀ concentration between the beta radiation attenuation monitor, a standardized low volume gravimetric reference sampler and a low volume sequential particulate sampler showed that PM₁₀ concentrations measured by the beta radiation attenuation monitor were higher than values given by the gravimetric samplers (mean ratio 1.17?±?0.11 and 1.21?±?0.08, respectively). Statistical and back trajectory analysis showed that elevated PM concentrations (PM₁₀, 93.8?±?49.1 μg/m³; PM_2.5: 102.9?±?59.9 μg/m³) are associated to desert dust events. In addition regional transport contributes significantly to the aerosol concentration levels whereas low aerosol concentrations were observed during storm episodes.     

Evaluation of Premature Mortality Caused by Exposure to PM2.5 and Ozone in East Asia: 2000, 2005, 2020

The aim of this study is to assess the premature mortality risks caused by exposure to particulate matter with aerodynamic diameter less than 2.5???m (PM_2.5) and ozone elevated concentrations for the years?2000, 2005, and 2020 in East Asia. The spatial distributions and temporal variations of PM_2.5 and ozone concentrations are simulated using the Models-3 Community Multiscale Air Quality Modeling System coupled with the Regional Emission Inventory in Asia. The premature mortality risks caused by exposure to PM_2.5 and ozone are calculated based on a relative risk (RR) value of 1.04 (95?% confidence interval (CI): 1.01?C1.08) for PM_2.5 concentrations above the annual mean limit of 10???g?m^?3 taken from the World Health Organization?CAir Quality Guideline and based on a RR value of 1.003 (95?% CI: 1.001?C1.004) for ozone concentration above 35?ppb of the SOMO35 index (the sum of ozone daily maximum 8-h mean concentrations above 35?ppb). We demonstrate one of the implications of the policy making in the area of environmental atmospheric management in East Asia by highlighting the annual premature mortalities associated with exposure to PM_2.5 concentrations that just meet an annual mean concentration of 10???g?m^?3, as well as ozone concentrations that have a daily zero SOMO35 index in vulnerable places. Our results point to a growing health risk that may endanger human life in East Asia. We find that the effect of PM_2.5 on human health is greater than the effect of ozone for the age group of 30?years and above. We estimate the corresponding premature mortality due to the effects of both ozone and PM_2.5 in East Asia for the years?2000 and 2005 to be around 316,000 and 520,000 cases, respectively. For future scenarios of the year?2020, policy succeed case, reference, and policy failed case, the estimated annual premature mortality rates are 451,000, 649,000, and 1,035,000 respectively.     

Atmospheric Emission Inventory for Natural and Anthropogenic Sources and Spatial Emission Mapping for the Greater Athens Area

A spatially, temporally and chemically resolved emission inventory for particulate matter and gaseous species from anthropogenic and natural sources was created for the Greater Athens Area (GAA; base year, 2007). Anthropogenic sources considered in this study include combustion (industrial, non-industrial, commercial and residential), industrial production, transportation, agriculture, waste treatment and solvent use. The annual gaseous pollutants (????x, SOx, non-methane volatile organic compounds (NMVOCs), CO and ????₃) and particulate matter (PM_2.5 and PM_2.5?C10) emissions were derived from the UNECE/EMEP database for most source sectors (SNAP 1?C9; 50?×?50 km²) and their spatial resolution was increased using surrogate spatial datasets (land cover, population density, location and emissions of large point sources, emission weighting factors for the GAA; 1?×?1 km²). The emissions were then temporally disaggregated in order to provide hourly emissions for atmospheric pollution modelling using monthly, daily and hourly disintegration coefficients, and additionally the chemical speciation of size-segregated particles and NMVOCs emissions was performed. Emissions from agriculture (SNAP 10) and natural emissions of particulate matter from the soil (by wind erosion) and the sea surface and of biogenic gaseous pollutants from vegetation were also estimated. During 2007 the anthropogenic emissions of CO, SOx, NOx, NMVOCs, NH₃, PM_2.5 and PM_2.5?C10 from the GAA were 151,150, 57,086, 68,008, 38,270, 2,219, 9,026 and 3,896 Mg, respectively. It was found that road transport was the major source for CO (73.3%), NMVOCs (31.6%) and NOx (35.3%) emissions in the area. Another important source for NOx emissions was other mobile sources and machinery (23.1%). Combustion for energy production and transformation industries was the major source for SOx (38.5%), industrial combustion for anthropogenic PM_2.5?C10 emissions (59.5%), whereas non-industrial combustion was the major source of PM_2.5 emissions (49.6%). Agriculture was the primary NH₃ source in the area (72.1%). Natural vegetation was found to be an important source of VOCs in the area which accounted for approximately the 5% of total VOCs emitted from GAA on a typical winter day. The contribution of sea-salt particles to the emissions of PM_2.5 was rather small, whereas the emissions of resuspended dust particles exceeded by far the emissions of PM_2.5 and PM_2.5?C10 from all anthropogenic sources.     

A Comparison of Trace Gases and Particulate Matter over Beijing (China) and Delhi (India)

Air pollution represents a significant fraction of the total mortality estimated by the World Health Organization (WHO) global burden of disease projec?t (GBD). The present paper discusses the characteristics of trace gases (O₃, NO, NO₂, and CO) and particulate matter (PM₁₀ and PM_2.5) in two Asian megacities, Delhi (India) and Beijing (China). A continuous measurement of trace gases and particulate matter are considered from 12 measuring sites in Beijing and 8 sites in Delhi. Over Beijing, the annual average of PM_2.5, PM₁₀, O₃, NO₂, and CO is, respectively, 85.3, 112.8, 58.7, and 53.4 μg/m³ and 1.4 mg/m³, and, respectively, over Delhi 146.5, 264.3, 24.7,and 19.8 μg/m³ and 1.73 mg/m³. From the spatial variations of pollutants, the concentrations of particulate matter and trace gases are observed to be much higher in the urban areas compared to the suburban areas. The higher average concentrations of PM₁₀ and PM_2.5 over Delhi and Beijing are observed during winter season compared with other seasons. The maximum diurnal variation of PM₁₀ concentration is observed during winter season over Beijing and Delhi. The comparison of trace gases shows that the O₃ concentrations during daytime are obviously higher compared with nighttime, and the highest diurnal variation of O₃ is observed during summer. The concentrations of CO are highest during winter season, and higher concentrations are observed during nighttime compared to daytime. The O₃ and CO show negative correlation over Beijing and Delhi. The negative correlation between O₃ and NO₂ is merely observed over Beijing, while CO and NO₂ concentrations, in contrast, show positive correlation over Beijing.     

A Study of PM2.5 and PM2.5-Associated Polycyclic Aromatic Hydrocarbons at an Urban Site in the Po Valley (Bologna, Italy)

PM_2.5 and PAHs bound to PM_2.5 were investigated in downtown Bologna, from January to June 2003, in order to determine the burden of the fine fraction in the aerosol of a typical urban environment of the Po Valley, a critical area in Northern Italy in terms of atmospheric pollution. The sampling campaign was divided into three parts: a winter sub-campaign, an intermediate campaign where PM_2.5 and PM₁₀ were simultaneously sampled and which identified PM_2.5 as the major component of PM₁₀, and a summer sub-campaign. Critical concentrations of both PM_2.5 and PAHs were observed in winter time; for example, in January 2003 the mean value for the 24-h average PM_2.5 concentration was 58 μg/m³, much higher than the annual arithmetic mean of 15 μg/m³ established by the US ambient air quality standard (NAAQS). Correspondingly, the mean value for benzo[a]pyrene (BAP) in PM_2.5 was 1.79 ng/m³, again higher than the annual mean of 1 ng/m³, required by European regulations for BAP in PM₁₀. In summer time the BAP concentration considerably decreases to 0.10 ng/m³ as the likely effect of photolysis and dilution on a higher boundary layer; PM_2.5 decreases too, but the mean concentration (22 μg/m³) is still higher than the NAAQS value. Further analysis included TEM microscopy of collected particles and correlations between PM_2.5, PAHs and gases (benzene, O₃, CO, NO₂, SO₂). All these observations identified on-road mobile sources as the main source of emissions and, in general, of the poor air quality level in the city of Bologna.     

Influence of Saharan Dust Transport Events on PM2.5 Concentrations and Composition over Athens

The evaluation of the contribution of natural sources to PM₁₀ and PM_2.5 concentrations is a priority especially for the countries of European south strongly influenced by Saharan dust transport events. Daily PM_2.5 concentrations and composition were monitored at an urban site at 14 m above ground level, at the National Technical University of Athens campus from February to December 2010. The typical dust constituents Si, Al, Fe, K, Ca, Mg, and Ti were determined by wavelength dispersive X-ray fluorescence spectrometry (WDXRF). Sulfur, a tracer of anthropogenic origin and major constituent of PM_2.5, was determined by both WDXRF and ionic chromatography. The contribution of dust and sulfates in PM_2.5 was calculated from the analytical determinations. An annual mean of 20 μg/m³ was calculated from the mean daily PM_2.5 concentrations data. Twenty-two per cent of daily concentrations of PM_2.5 reached or exceeded the EU annual target concentration of 25 μg/m³. The exceedances occurred during 13 short periods of 1–4 days. Back-trajectory analysis was performed for these periods in order to identify the air masses origin. From these periods, ten periods were associated to Saharan dust transport events. The most intense dust transport event occurred between February 17th and 20th and was responsible for the highest recorded PM_2.5 concentration of 100 μg/m³ where the dust contribution in PM_2.5 reached 96 %. The other dust transport events were less intense and corresponded to less pronounced enhancements of PM_2.5 concentrations, and their contribution ranged from 15 to 39 % in PM_2.5 concentrations. Air masses originated from northwest Africa while the influence of central Sahara was quite smaller.     

Characterization of Elemental Species in PM2.5 Samples Collected in Four Cities of Northeast China

A monitoring program of particulate matter was conducted at eight sampling sites in four highly industrialized cities (Shenyang, Anshan, Fushun, and Jinzhou) of Liaoning Province in Northeast China to identify the major potential sources of ambient PM_2.5. A total of 814 PM_2.5 and PM_2.5–10 samples were collected between 2004 and 2005. All PM samples were collected simultaneously in four cities and analyzed gravimetrically for mass concentrations. A sum of 16 elemental species concentrations in the PM samples were determined using inductively coupled plasma atomic emission spectroscopy. Annual means of PM_2.5 concentrations ranged from 65.0 to 222.0 μg m^?3 in all the eight sampling sites, and the spatial and seasonal variations were discussed. Enrichment factors were calculated, and Cr, Cu, Zn, As, Cd, and Pb will be pollution-derived elements. Site-to-site comparisons of PM_2.5 species in each city were examined using coefficient of divergence, revealing that the two sites in each city are similar in elemental species. Principle component analysis was used for preliminary source analysis of PM_2.5. Three or four factors in each city were isolated, and similar sources (crustal source, coal combustion, vehicle exhaust, iron making, or some other metallurgical activities) were identified at four cities.     

Measurement Uncertainty of Sulphur and Nitrogen Containing Inorganic Compounds By 1-Stage and 2-Stage Filter-pack Methods

The sampling and analysis properties of 1-stage and 2-stage filter-pack methods were studied in detail in monitoring of sulphur and nitrogen containing inorganic gases and particles (sulphur dioxide, sulphate, sum of nitric acid and nitrate and total ammonium). The limit of detection and the limit of quantitation for 24-h samples were estimated using the results of a short-term field experiment completed with available data from long-term monitoring and internal quality assurance. Furthermore, the combined expanded measurement uncertainty including sampling and analysis (U_tot) was estimated for filter-pack methods in order to give a tool for distinguishing long-term trends in air quality from the measurement variability. U_tot was found to be very near the analytical uncertainty when measuring higher air concentration levels, being ± 4.0% for sulphur concentrations?>?1.0 μg m^?3, ± 3.0% for sulphate concentrations?>?0.5 μg m^?3, ± 3.5% for the sum of nitrate and nitric acid concentrations?>?0.3 μg m^?3 and ± 4.5% for total ammonium concentrations?>?0.8 μg m^?3. At the lower air concentration range U_tot increases significantly due to the field blank values. The precision of the 24-h filter-pack sample results expressed by means of modified median absolute difference (M.MAD) and coefficient of variance (CoV) gave 8.3% for sulphur dioxide and 5.4% for particulate sulphate. For the sum of gaseous nitric acid and particulate nitrate the CoV was 5.5% and for total ammonium 4.3%. In addition the suitability of the 24-h filter-pack methods in weekly sampling was proved.     

Influence of the 23 October 2002 Dust Storm on the Air Quality of Four Australian Cities

Widespread drought and record maximum temperatures in eastern Australia produced a large dust storm on 23 October, 2002 which traversed a large proportion of eastern Australia and engulfed communities along a 2000 km stretch of coastline from south of Sydney (NSW) to north of Mackay (Queensland). This event provided an opportunity for a study of the impacts of rural dust upon the air quality of four Australian cities. A simple model is used to predict dust concentrations, dust deposition rates and particle size characteristics of the airborne dust in the cities. The total dust load of the plume was 3.35 to 4.85 million tones, and assuming a (conservative) plume height of 1500 m, 62–90% of this dust load was deposited in-transit to the coast. It is conservatively estimated that 3.5, 12.0, 2.1 and 1.7 kilotonnes of dust were deposited during the event in Sydney, Brisbane, Gladstone and Mackay, respectively. In the South East Queensland region, this deposition is equivalent to 40% of the total annual TSP emissions for the region. The event increased TSP, PM₁₀ and PM_2.5 concentrations and reduced the visibility beyond the health and amenity guidelines in the four cities. For example, the 24-h average PM₁₀ concentrations in Brisbane and Mackay, were 161 and 475 μg m^?3 respectively, compared with the Australian national ambient air quality standard of 50 μg m^?3. The 24-h average PM_2.5 concentration in Brisbane was 42 μg m^?3, compared with the national advisory standard of 25 μg m^?3. These rural dusts significantly increased PM₁₀/TSP ratios and decreased PM_2.5/PM₁₀ ratios, indicating that most of the particles were between PM_2.5 and PM₁₀.     

Human Health Impact of Exposure to Airborne Particulate Matter in Pearl River Delta, China

To evaluate the potential public health impact of exposure to airborne particulate matter, concentrations of PM₁₀ and PM_2.5 were measured at 16 monitoring stations in Pearl River Delta. Epidemiological studies were collected, and meta-analysis method was used to get the exposure-response functions for health effects on mortality of residents in China. Chinese studies reported somewhat lower exposure-response coefficients as compared with studies abroad. Both Poisson model and life-table approach were used to estimate the health effects including acute effects and chronic effects. For short-term exposure, 2,700 (95% confidence interval (CI), 2,200?C3,400) premature deaths would be prevented annually if PM₁₀ daily concentrations reduced to below World Health Organization (WHO) guideline value. Much more benefits would be gained for long-term exposure. The annual avoidable deaths would be 42,000 (95% CI, 28,000?C55,000) and 40,000 (95% CI, 23,000?C54,000) for PM₁₀ and PM_2.5, respectively, if the particulate matter annual concentrations were reduced to below WHO guideline values. And the average lifespan of residents would prolong 2.57?years for PM₁₀ and 2.38?years for PM_2.5 if reducing the PM annual concentrations. The benefits varied greatly in different areas and different manage strategies should be carried out to protect human health effectively.     

Assessing the Influence of Different Atmospheric and Soil Mercury Concentrations on Foliar Mercury Concentrations in a Controlled Environment

This study vividly presents results from a seasonal particulate matter measurement campaign conducted at world’s largest ship-breaking yard i.e., Alang-Sosiya (Gujarat, India) at six locations and a reference station at Gopnath which is 30 km south of this ship-breaking yard. The collected suspended particulate matter (SPM) 24-h samples were critically analyzed for heavy metals (Pb, Cd, Co, Ni, Cr, Mn, Fe, Cu, Zn). The average concentration of SPM within the ship-breaking yard during the investigation was 287.5 ± 20.4 μg m^?3 and at reference station it was 111.13 ± 5.81 μg m^?3. These values are found to be in excess of the permitted national standards. The levels of heavy metals at Alang-Sosiya are very high as compared to US EPA and WHO guidelines. The mean concentrations of all metals are in the order: Fe >>Zn >Cu > Mn > Cd >Pb > Co >Ni >Cr. The results on enrichment factors (EF) suggest that most of the metals in the ship-breaking yard exhibit EF values of near or above 100 which must have been comprehensively affected by ship-breaking activities. Metal data was used to evaluate the role of spatial factors on their distribution characteristics. Thereafter, factor analysis was carried out to identify the main components liable for the variance of the data set.     

An Assessment of the Mobile Source Contribution to PM10 and PM2.5 in the United States

Mobile sources are significant contributors to ambient particulate matter (PM) in the United States. As the emphasis shifts from PM₁₀ to PM_2.5, it becomes particularly important to account for the mobile source contribution to observed particulate levels since these sources may be the major contributor to the fine particle fraction. This is due to the fact that most mobile source mass emissions have an aerodynamic diameter less than 2.5 µm, while the particles of geological origin that tend to dominate the PM₁₀ fraction generally have an aerodynamic diameter greater than 2.5 µm. A common approach to assess the relative contributions of sources to observed particulate mass concentrations is the application of source apportionment methods. These methods include material balance, chemical mass balance (CMB), and multivariate receptor models. This paper describes a number recent source attribution studies performed in the United States in order to evaluate the range of the mobile source contribution to observed PM. In addition, a review of the methods used to apportion source contributions to ambient particulate loadings is presented.     

Effects of organic material amendment and water content on NO, N2O, and N2 emissions in a nitrate-rich vegetable soil

Amending vegetable soils with organic materials is increasingly recommended as an agroecosystems management option to improve soil quality. However, the amounts of NO, N₂O, and N₂ emissions from vegetable soils treated with organic materials and frequent irrigation are not known. In laboratory-based experiments, soil from a NO ₃ ^? -rich (340 mg N?kg^?1) vegetable field was incubated at 30°C for 30 days, with and without 10 % C₂H₂, at 50, 70, or 90 % water-holding capacity (WHC) and was amended at 1.19 g?C kg^?1 (equivalent to 2.5 t?C ha^?1) as Chinese milk vetch (CMV), ryegrass (RG), or wheat straw (WS); a soil not amended with organic material was used as a control (CK). At 50 % WHC, cumulative N₂ production (398–524 μg N?kg^?1) was significantly higher than N₂O (84.6–190 μg N?kg^?1) and NO (196–224 μg N?kg^?1) production, suggesting the occurrence of denitrification under unsaturated conditions. Organic materials and soil water content significantly influenced NO emissions, but the effect was relatively weak since the cumulative NO production ranged from 124 to 261 μg N?kg^?1. At 50–90 % WHC, the added organic materials did not affect the accumulated NO ₃ ^? in vegetable soil but enhanced N₂O emissions, and the effect was greater by increasing soil water content. At 90 % WHC, N₂O production reached 13,645–45,224 μg N?kg^?1 from soil and could be ranked as RG?>?CMV?>?WS?>?CK. These results suggest the importance of preventing excess water in soil while simultaneously taking into account the quality of organic materials applied to vegetable soils.     

Air Pollution Processing by Radiation Fogs

Several fog episodes occurred in California’s San Joaquin Valley during winter 2000/2001. Measurements revealed the fogs to generally be less than 50 m deep, but to contain high liquid water contents (frequently exceeding 200 mg/m³) and large droplets. The composition of the fog water was dominated by ammonium (median concentration?=?608 μN), nitrate (304 μN), and organic carbon (6.9 ppmC), with significant contributions also from nitrite (18 μN) and sulfate (56 μN). Principal organic species included formate (median concentration?=?32 μN), acetate (31 μN), and formaldehyde (21 μM). High concentrations of ammonia resulted in high fog pH values, ranging between 5.8 and 8.0 at the core measurement site. At this high pH aqueous phase oxidation of dissolved sulfur dioxide and reaction of S(IV) with formaldehyde to form hydroxymethanesulfonate are both important processes. The fogs are also effective at scavenging and removal of airborne particulate matter. Deposition velocities for key solutes in the fog are typically of the order of 1–2 cm/s, much higher than deposition velocities of precursor accumulation mode aerosol particles. Variations were observed in deposition velocities for individual constituents in the order NO₂ ^??>?fogwater?>?NH₄ ⁺?>?TOC ～ SO₄ ^2??>?NO₃ ^?. Nitrite, observed to be enriched in large fog drops, had a deposition velocity higher than the average fogwater deposition velocity, due to the increase in drop settling velocity with size. Species enriched in small fog drops (NH₄ ⁺, TOC, SO₄ ^2?, and NO₃ ^?) all had deposition velocities smaller than observed for fogwater. Typical boundary layer removal rates for major fog solute species were estimated to be approximately 0.5–1 μg m^?3 h^?1, indicating the important role regional fogs can play in reducing airborne pollutant concentrations.     

Diurnal Characteristics of Suspended Particulate Matter and PM<Subscript>2.5</Subscript> in the Urban and Suburban Atmosphere of the Kanto Plain,Japan

Suspended particulate matter (SPM) and PM_2.5 in the urban and suburban atmosphere of the Kanto Plain of Japan, which includes the Tokyo metropolitan area, during the period 22–26 July 2002 were characterized. Samples of SPM and PM_2.5 were collected by low-volume samplers at 6-h intervals at Suginami, Saitama, and Kisai. At all the sites, the major components of SPM and PM_2.5 were organic carbon (OC), elemental carbon (EC), and sulfate. The ion balance, the size distributions of the ionic species, and the high correlation between SO₄ ^2? and NH₄ ⁺ indicated that the main chemical form of sulfate was (NH₄)₂SO₄. The OC/EC ratios were larger in the daytime than in the nighttime. The correlation coefficients of OC, OC/EC, and SO₄ ^2? with ozone concentrations at inland sites (Saitama, Kisai) were higher than those at the coastal site (Suginami). Bound water and hydrogen and oxygen atoms associated with OC, the amounts of which were estimated with a mass closure model, contributed substantially to the total particle mass. The chemical characteristics of the particles indicated that two mechanisms led to high concentrations of SPM and PM_2.5: (i) an active photochemical process produced high concentrations of OC and sulfate, leading to a high concentration of (NH₄)₂SO₄ in the particles and to production of secondary organic aerosols; (ii) stable meteorological conditions resulted in accumulation of primary particles, mainly emitted from vehicle exhaust, resulting in high concentrations of OC and EC.     

A Study of Airborne Selected Metals and Particle Size Distribution in Relation to Climatic Variables and their Source Identification

Ten selected metals (Na, K, Fe, Zn, Pb, Mn, Cr, Co, Ni & Cd) were estimated in total suspended particulate (TSP) samples collected on glass fibre filters in urban Islamabad, Pakistan, from October 2002 to May 2003, using a high volume sampling technique. The wet digestion method (HNO₃/HClO₄) was used for metal analysis by the flame atomic absorption spectrophotometry (FAAS) method. Maximum mean contribution was noted for Na (1.949 μg m^?3), followed by K (0.900 μg m^?3), Zn (0.603 μg m^?3), Fe (0.584 μg m^?3) and Pb (0.214 μg m^?3). The particle size determination on % volume basis for four fractions (PM_{< 2.5}, PM_2.5–10, PM_10–100& PM_{> 100}) was also carried out. PM_10–100 were found to be the most abundant in the local atmosphere followed by PM_2.5–10, while the respirable fraction (PM_{< 2.5}) and giant fraction (PM_{> 100}) showed comparable and lower levels. The trace metals were found to be mainly associated with PM_{< 2.5} and PM_2.5–10. The influence of climatic variables on toxic trace metals and particle size fractions was also investigated statistically and it was revealed that temperature has a significant correlation with fine particle fractions and airborne trace metal levels. The source identification was carried out by Principal Component Analysis and Cluster Analysis. Four metal sources were identified: industrial (32.6%), soil-derived dust (21.9%), traffic/road dust (19.8%), and metallurgical/garbage incineration (12.4%). The metal levels were also compared with those reported for other parts around the world.     

Rural O3 Levels in the Middle Ebro Basin During the Plant Growing Season

Ground-level dynamics of O₃, NO _x and benzene, toluene, ethylbenzene and xylenes were characterised at rural sites in the medium Ebro River Basin (Northern Spain) from April to September (2003–2007) and by means of automated and passive monitoring. The study registered high O₃ levels within the area, which were influenced by traffic emissions, and a monthly evolution of these levels consistent with the occurrence of a broad summer maximum, typical of polluted areas. The mean ozone concentration registered in the studied area by means of passive sampling was 87?±?12 μg m^?3. The 2008/50/EC objective value for the protection of vegetation was widely exceeded during this study (AOT40?=?57,147?±?14,114 μg m^?3 h), suggesting that current ambient levels may pose a risk for crops and vegetation in this important agroindustrial region.     

Geochemistry of Tungsten and Arsenic in Aquifer Systems: A Comparative Study of Groundwaters from West Bengal, India, and Nevada, USA

The objective of the current study was to estimate the dose in human tissues after inhalation exposure to airborne particulate matter-bound metals at a landfill site. Field measurements have revealed that the 8-h permissible exposure limit set by the Occupational Safety and Health Administration for particulate matter (PM₁₀) was not exceeded for the working personnel at an outdoor weighing facility in the Akrotiri landfill (Chania, Greece). However, PM₁₀ concentrations were exceeding the EU health protection standards (50 μg/m³). Furthermore, dust emanating from landfill operations contains traces of heavy metals due to the nature of materials (e.g., sludge, batteries) which have been deposited over the lifetime of the landfill. In addition, particulate matter-bound metals concentrations at the landfill are enhanced by refuse truck emissions (e.g., exhaust, tire wear dust, brake wear dust, road surface wear dust and resuspension of deposited PM on a road surface) and resuspension from the surface of the composting site. Estimations of particle-bound metals dose in the human body were performed for arsenite (AS^III), lead (Pb) and cadmium (Cd). The Exposure Dose Model (ExDoM) in conjunction with a Physiologically Based PharmacoKinetic (PBPK) model was applied to determine the dose for an adult Caucasian male worker. The ExDoM was used to estimate the human exposure and the deposition, dose, clearance, retention of particulate matter-bound metals in the human respiratory tract and the mass transferred to the gastrointestinal tract and blood. The PBPK model was developed to describe the movement of metals from the blood into the tissues as a blood-flow-limited model. The results showed that after 1 day of exposure to PM_AsIII, the major accumulation occurs in the lung, muscle and liver. In addition, for PM_Pb, the major accumulation occurs in the bone, blood and muscle whereas as regard PM_Cd the major accumulation occurs in the other tissues (the rest of the body), kidney and liver. The results indicate an increased health risk for an adult Caucasian male worker at the landfill site due to exposure to elevated particulate matter concentrations and their associated metallic content.     

Evaluation of greenhouse gas emissions in a Miscanthus sinensis Andersson-dominated semi-natural grassland in Kumamoto,Japan

Increasing greenhouse gas emissions from anthropogenic activities continue to be a mounting problem worldwide. In the semi-natural Miscanthus sinensis Andersson; grasslands of Aso, Kumamoto, Japan, which have been managed for thousands of years, we measured soil methane (CH₄) and nitrous oxide (N₂O) emissions before and after annual controlled burns. We estimated annual soil carbon (C) accumulation, and CH₄ and N₂O emissions induced by biomass burning in 2009 and 2010, to determine the impacts of this ecosystem and its management on global warming. Environmental factors affecting soil CH₄ and N₂O fluxes were unknown, with no effect of annual burning observed on short-term soil CH₄ and N₂O emissions. However, deposition of charcoal during burning may have enhanced CH₄ oxidation and N₂O consumption at the study site, given that emissions (CH₄: ?4.33 kg C ha^?1 yr^?1, N₂O: 0.17 kg N ha^?1 yr^?1) were relatively lower than those measured in other land-use types. Despite significant emission of CH₄ and N₂O during yearly burning events in early spring, the M. sinensis semi-natural grassland had a large annual soil C accumulation, which resulted in a global warming potential of ?4.86 Mg CO₂eq ha^?1 yr^?1. Consequently, our results indicate that long-term maintenance of semi-natural M. sinensis grasslands by annual burning can contribute to the mitigation of global warming.     

Human and climatic drivers of land and water use from 1997 to 2019 in Tarim River basin,China

Climate and human activities change spatial and temporal distribution of water and land use. The Tarim River, the largest inland river in China, faced a long-term exploitation of land and water over a rapid economic development. We analyzed land and water use from 1997 to 2019 in Tarim River Basin by Landsat images, and data on hydrology, climate, population, economy and PM_2.5 (air particulate matter ≤2.5 μm). Agricultural land expanded the fastest (4–11%), followed by natural vegetation (15–16%) and water area (4–5%) with population and economic increase. Air quality (PM_2.5 μg m⁻³) improved in upper (62–27) and middle (48–17) reaches. The water area in lower increase 5% because of ecological water delivery since 2000. Land use in the lower reach was dominated by agriculture, where the downstream runoff consumption increased by 6.8 times. The average annual air temperature and precipitation gradually increased by 0.5 °C and 51 mm in source and 0.9 °C and 30 mm in main reaches. The average annual water consumption in upper and middle reaches was 4 × 10⁹ m³, accounting for 87% of input runoff in the main reach. Water consumption in middle reach increased by 33 times in 2009–2017. The industry structure was changing from primary to secondary and tertiary industry. To sum up, implementation of water saving strategies and ecological water delivery restored local ecology. Sustainable strategies should be applied facing industrialization. Furthermore, changing the industry structure and restoring the degraded farmlands to grasslands or forests would keep sustainability of Tarim River Basin.