Pattern Classification of Volatile Organic Compounds in Various Indoor Environments

The purpose of this study was to survey the distribution patterns of volatile organic compounds (VOCs) and formaldehyde in the various indoor environments using cluster analysis. We investigated VOCs and formaldehyde in subway stations, underground shopping areas, medical centers, maternity recuperation centers, public childcare centers, large stores, funeral homes, and indoor parking lots from June 2005 to May 2006 (9 p.m. to 6 a.m.). The concentration of total volatile compounds (TVOCs) in maternity recuperations was 2,605.7 ??g/m³, which was higher than that stated in the guideline and other chosen facilities. TVOCs in public childcare centers were 1,951.6 ??g/m³, which also exceeded the guideline. Moreover, the concentration of TVOCs in every facility exceeded the guideline of the Ministry of Environment, Korea. In the case of formaldehyde, the mean concentration of 336.5 ??g/m³ found only in public childcare centers exceeded the 120 ??g/m³ stated in the guideline. Finally, by applying cluster analysis, three patterns of the indoor air pollutions were distinguished. In the results of the analysis, concentrations of TVOCs and formaldehyde of cluster 3 were higher than clusters 1 and 2, which were 2,561.4 and 184.9 ??g/m³, respectively.     

Evaluation of Air Pollution Burden from Contribution of Motorcycle Emission in Bangkok

This study investigated the relationship between exhaust emission from motorcycles and ambient air quality in Bangkok Metropolitan Region (BMR). The test result revealed that averagepollutant concentrations of the test motorcycles in terms of hydrocarbon, carbon monoxide and nitrogen dioxide were 8.38, 16.69 and 0.04 g km^-1, respectively. The finding also indicated that two-stroke motorcycles emitted 1.5 and 5 times more carbon monoxide and hydrocarbon emission, respectively perkilometer driven than do four-stroke motorcycles. Four air sampling stations were strategically established to evaluate the air pollution problems in Bangkok arising from vehicle exhaust emission. Investigation was carried out to determine the correlation between average air pollutant concentration with different traffic configuration in each traffic zone of Bangkok Metropolitan Region (BMA) during peak/non peak hours, day/night times and weekday/weekend. The average concentrationsof PM₁₀ particulate matter, carbon monoxide, nitrogen dioxide and sulphur dioxide in Bangkok street air were found tobe 84.33 μg m^-3 (24 hr ave.), 7.05 mg m^-3 (8 hr ave.), 56.74 μg m^-3 (1 hr ave.) and 9.60 μg m^-3 (24 hr ave.), respectively.     

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.     

Concentration and Exposure Evaluation of Perchlorate in Size-Segregated Airborne Particulate Matter from Changsha,China

As a newly emerging persistent environmental contaminant, perchlorate (ClO₄ ^?) has adverse effects on thyroid function by inhibiting iodide uptake and could result in neurodevelopment deficits. Our study was performed to investigate the concentration of perchlorate in size-segregated airborne particulate matter (APM) and evaluate its human exposure for children and adults. In this study, 45 size-segregated APM samples were collected from Changsha, China, during July 20 to July 31, 2016. The total APM concentrations ranged from 93.367 to 253.271 μg/m³ (mean 154.651 ± 59.175 μg/m³), and a bimodal size distribution was observed during the sampling period. The concentrations of perchlorate in size-segregated APM were in the range of 0.05–4.99 ng/m³ (mean 2.03 ng/m³). Exposure evaluation indicated that the ingestion was the predominant exposure pathway for daily intake of perchlorate via size-segregated APM, and children are more likely to intake more perchlorate via APM than adults. We suggested that the risk of exposure to perchlorate for children is worthy of attention, and a further study is required, especially for seasonal variations.     

The Use of AERMOD Air Pollution Dispersion Models to Estimate Residential Ambient Concentrations of Elemental Mercury

Source-oriented models are ideally suited to examine the impact of terrain and meteorology and source factors such as stack height when evaluating exposures to air pollutants. A source-oriented, Gaussian plume air pollution dispersion model AERMOD was used to estimate the spatial distribution of elemental mercury (Hg⁰) from a typical coal-fired boiler emitting 0.001 g Hg⁰/s. Hg⁰ was chosen because of its health impact related to potential neurological and reproductive effects which may be especially important for high-risk populations. Results from four simulations using meteorological data from 2004 were compared for flat and hilly terrain from 20- and 55-m stacks at a distance of 1,350 m from the source. Variations within a quadrant were affected primarily by topography. For the 20-m stack, the average annual ambient concentration for individuals living within the northeast (NE) quadrant was significantly lower at 2.5 ng Hg⁰/m³ (P?<?0.001; confidence interval (CI), 2.4?C2.6) in flat terrain versus 3.3 ng Hg⁰/m³ in hilly (P?<?0.001; CI, 1.2?C1.3). NE concentrations of the source showed high spatial variability attributed to topography with 1-h maximums of 4.0 ng Hg⁰/m³ flat versus 7.1 ng Hg⁰/m³ hilly. Not unexpectedly, average annual concentrations were considerably lower for the 55-m stack although topography remained a significant variable with 0.1 ng Hg⁰/m³ in flat terrain (p?<?0.001; CI, 0.11?C0.13) and double that exposure at 0.2 ng Hg⁰/m³ in hilly terrain (p?<?0.001; CI, 0.16?C0.18). Annual average mercury concentrations due to emissions from the 20-m stack were ~20 times higher than ambient concentrations associated with the 55-m stack. A sensitivity analysis was performed for meteorological effects, using meteorological data from years 2001?C2005. Varying the roughness factor had no significant effect on the results. For all simulations, the highest concentrations were located in the NE quadrant. During 2001?C2005, the highest average annual ambient Hg concentration ranged from 6.2 to 7.0 ng Hg⁰/m³ for the 20-m stack and 0.3?C0.5 ng Hg⁰/m³ for the 55-m stack. Thus, this model is robust. These results demonstrate the usefulness of a source-oriented model such as AERMOD for incorporating multiple factors for estimating air pollution exposures for communities near point sources. The importance of considering topography, meteorology, and source characteristics when placing air samplers to measure air quality and when using buffer zones to estimate ambient residential exposures is also illustrated. Residential communities in hilly terrain near industrial point sources may have between two to three times the exposures as those in flat terrain. Exposures will vary depending on the stack height of the point source.     

A Synoptic Survey of Nitrogen and Phosphorus in Tributary Streams and Great Rivers of the Upper Mississippi, Missouri, and Ohio River Basins

We combined stream chemistry and hydrology data from surveys of 436 tributary stream sites and 447 great river sites in the Upper Mississippi, Missouri and Ohio River basins to provide a regional snapshot of baseflow total nitrogen (TN) and total phosphorus (TP) concentrations, and to investigate the relationships between land use and stream chemistry. Catchments in the Upper Mississippi River basin had more land in agricultural uses (51%) than the Missouri or Ohio River basin catchments (25% and 29%, respectively). The difference in agriculture is reflected in the TN concentrations in tributary streams and the great rivers: 5,431 and 2,112 ??g L^?1 for the Upper Mississippi, 1,751 and 978 ??g L^?1 for the Missouri, and 1,074 and 1,152 ??g L^?1 for the Ohio River basins. This agricultural effect was not as evident for tributary stream or great river TP concentrations: 165 and 181 ??g L^?1 in the Upper Mississippi, 177 and 171 ??g L^?1 in the Missouri, and 67 and 53 ??g L^?1 in the Ohio River basins. We set reference thresholds based on the 75th percentile TN and TP concentrations at our least disturbed sites. The TN threshold was exceeded for 50?C63% of the tributary stream and 16?C55% of great river lengths, with the greatest proportion in the Upper Mississippi River basin. The TP threshold was exceeded in 32?C48% of tributary stream and 12?C41% of great river lengths. Tributary stream N/P ranged from 67:1 (Ohio) to 210:1 (Upper Mississippi); river N/P ranged from 20:1 (Missouri) to 60:1 (Ohio). N/P indicated that potential N-limitation occurred in 10?C21% of total tributary stream length and in 0?C46% of great river length; potential P-limitation ranged from 60?C83% of cumulative tributary stream length and from 21?C98% of cumulative great river length. Total N flux (concentration × discharge) was highest in the Upper Mississippi River basin; TP flux was lowest in the Ohio River basin. River TN yields and TP yields for both tributary streams and great rivers, was not significantly different between the sub-basins. Our study empirically links catchment land use and stream chemistry, and demonstrates using monitoring data for estimating nutrient yields at a large regional scale.     

Wet and Dry Deposition Fluxes of Polychlorinated Biphenyls (PCBs) in an Urban Area of Turkey

Atmospheric polychlorinated bihenyls (PCBs) deposit by dry and wet deposition mechanisms, and therefore they constitute a significant polluting source for lands and surface waters. Various samplers have been used to determine the PCB pollution level resulting from deposition. In the presented study, a modified wet deposition sampler (WDS) was used for sampling both wet and dry deposition samples with the same instrument by which wet deposition reservoir of the WDS is opened and dry deposition reservoir is closed when rain starts. Wet and dry deposition samples were collected between June 2008 and June 2009. In the samples taken from BUTAL which is known as an urban area with heavy traffic, ??PCB dry deposition fluxes were determined as 18?±?10 ng/m²??day, and wet deposition fluxes for dissolved and particle phase were measured as 480?±?1,185 and 475?±?1,000 ng/m²??day, respectively. The dissolved and particle-phase PCB concentrations in rain were 10?±?13 and 13?±?14 ng/l, respectively. The contribution of wet deposition to total PCB deposition was determined as 52%. PCB concentrations in the ambient air were measured to be 370?±?200 and 20?±?20 pg/m³ for gas and particle phases, respectively. Washout ratio was determined by proportioning rain concentration to concentration in air. The washout ratios of the samples were between 1,675?C311,800 and 12,775?C2,511,120 for dissolved and particulate phases, respectively.     

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.     

Annual and Seasonal Variations of Trace Metals in Atmospheric Suspended Particulate Matter in Islamabad, Pakistan

Total Suspended particulate matter (TSP) in urban atmosphere of Islamabad was collected using a high volume sampling technique for a period of one year. The nitric acid–perchloric acid extraction method was used and the metal contents were estimated by atomic absorption spectrophotometer. The highest mean concentration was found for Ca at 4.531 µg/m³, followed by Na (3.905 µg/m³), Fe (2.464 µg/m³), Zn (2.311 µg/m³), K (2.086 µg/m³), Mg (0.962 µg/m³), Cu (0.306 µg/m³), Sb (0.157 µg/m³), Pb (0.144 µg/m³) and Sr (0.101 µg/m³). On an average basis, the decreasing metal concentration trend was: Ca > Na > Fe > Zn > K > Mg > Cu > Sb > Pb > Sr > Mn > Co > Ni > Cr > Li > Cd ≈ Ag. The TSP levels varied from a minimum of 41.8 to a maximum of 977 µg/m³, with a mean value of 164 µg/m³, which was found to be higher than WHO primary and secondary standards. The correlation study revealed very strong correlations (r?>?0.71) between Fe–Mn, Sb–Co, Na–K, Mn–Mg, Pb–Cd and Sb–Sr. Among the meteorological parameters, temperature, wind speed and pan evaporation were found to be positively correlated with TSP, Ca, Fe, K, Mg, Mn and Ag, whereas, they exhibited negative relationships with relative humidity. On the other hand, Pb, Sb, Zn, Co, Cd and Li revealed significant positive correlations with relative humidity and negative with temperature, wind speed and pan evaporation. The major sources of airborne trace metals identified with the help of principle component analysis and cluster analysis were industrial emissions, automobile exhaust, biomass burning, oil combustion, fugitive emissions, resuspended soil dust and earth crust. The TSP and selected metals were also studied for seasonal variations, which showed that Na, K, Zn, Cu, Pb, Sb, Sr, Co and Cd peaked during the winter and remained lowest during the summer, while Ca, Fe, Mg and Mn were recorded highest during the spring.     

Production of Energy and Biofertilizer from Cattle Wastewater in Farms with Intensive Cattle Breeding

This study evaluates the treatment efficacy and biogas yield of an integrated system composed of a plug-flow biodigester (with sludge recirculation) followed by polishing in a stabilization pond. The system was operated in real scale for 12 months at ambient temperature and under continuous flow. The volumetric yields of biogas varied according to the organic loads applied, between 114 and 294 Kg COD day^?1, reaching levels of 0.026 to 0.173 m³ m^?3 day^?1, with concentrations of CH₄ between 56 and 70%. The monthly biogas productions were between 378.5 and 2186.1 m³ month^?1 equal to an energy potential of approximately 2070 to 19,168 KWh month^?1.The average yearly removals of BOD_5,20 and COD by the integrated treatment system were 70 and 86%, respectively. The average annual removals of NH₄ and TKN were 88.5 and 85.5%, respectively. The pH values were always near neutral, and the alkalinity was in ranges propitious for anaerobic digestion. The results of this study indicate good efficacy in terms of removal of organic matter and nitrogen compounds, with the added benefits of generation of energy and use of the treated effluent as biofertilizer, enabling significant cost reductions to cattle farmers.     

Airborne lead pollution in Metropolitan Taipei (Republic of China)

To examine the spatial variation of airborne lead in Taipei, a field study was conducted during the summer and fall of 1991. Samples were collected 2–4 times daily at several sites for the determination of airborne lead. Results indicate that the average of air lead concentration of Taipei city is 0.70±0.39 μg/m³ and eighty-eight percent of particles are smaller than 10 pm. From high to low polluted area, the fine particle concentrations are 0.83, 0.51, 0.29 μg/m³ The lead concentration of particulates < 10 μm on 2nd, 7th, and 14th floors of a building are 0.75, 0.60, 0.55 μg/m³, and appears to be little difference among vertical dispersions. The air lead concentrations (da < 10 μm) on roadside, side walk and covered walk way from the vehicle emission source of a main road are 0.83, 0.78, 0.87 μg/m³ the highest is on the covered walk way. For lead concentrations (da < 10 μm) on the main street, side street and alley of an area are 0.34, 0.37, 0.35 μg/m³ the result indicates lead concentrations on these pathways are not significantly different.     

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.     

Assessment of Bacterial and Fungal Aerosol in Different Residential Settings

The concentration and size distribution of bacterial and fungal aerosol was studied in 15 houses. The houses were categorized into three types, based on occupant density and number of rooms: single room in shared accommodation (type I), single bedroom flat in three storey buildings (type II) and two or three bedroomed houses (type III). Sampling was undertaken with an Anderson six-stage impactor during the summer of 2007 in the living rooms of all the residential settings. The maximum mean geometric concentration of bacterial (5,036 CFU/m³, ± 2.5, n?=?5) and fungal (2,124 CFU/m³, ± 1.38, n?=?5) aerosol were in housing type III. The minimum levels of indoor culturable bacteria (1,557 CFU/m³, ±1.5, n?=?5) and fungal (925 CFU/m³, ±2.9, n?=?5) spores were observed in housing type I. The differences in terms of total bacterial and fungal concentration were less obvious between housing types I and II as compared to type III. With reference to size distribution, the dominant stages for culturable bacteria in housing types I, II and III were stage 3 (3.3–4.7 μm), stage 1 (7 μm and above) and stage 5 (1.1–2.1 μm), respectively. Whereas the maximum numbers of culturable fungal spores were recovered from stage 2 (4.7–7 µm), in housing type I, and from stage 4 (2.1–3.3 μm) in both type II and III houses. The average geometric mean diameter of bacterial aerosol was largest in type I (4.7 μm), followed by type II (3.89 μm) and III (1.96 μm). Similarly, for fungal spores, type I houses had the highest average mean geometric diameter (4.5 μm), while in types II and III the mean geometric diameter was 3.57 and 3.92 μm, respectively. The results indicate a wide variation in total concentration and size of bioaerosols among different residential settings. The observed differences in the size distributions and concentrations reflect their variable airborne behaviour and, as a result, different risks of respiratory exposure of the occupants to bioaerosols in various residential settings.     

Impacts of nitrogen addition on the carbon balance in a temperate semiarid grassland ecosystem

Understanding carbon (C) cycling and sequestration in vegetation and soils, and their responses to nitrogen (N) deposition, is important for quantifying ecosystem responses to global climate change. Here, we describe a 2-year study of the C balance in a temperate grassland in northern China. We measured net ecosystem CO₂ exchange (NEE), net ecosystem production (NEP), and C sequestration rates in treatments with N addition ranging from 0 to 25 g N m^?2 year^?1. High N addition significantly increased ecosystem C sequestration, whose rates ranged from 122.06 g C m^?2 year^?1 (control) to 259.67 g C m^?2 year^?1 (25 g N). Cumulative NEE during the growing season decreased significantly at high and medium N addition, with values ranging from ?95.86 g C m^?2 (25 g N) to 0.15 g C m^?2 (5 g N). Only the highest N rate increased significantly cumulative soil microbial respiration compared with the control in the dry 2014 growing season. High N addition significantly increased net primary production (NPP) and NEP in both years, and NEP ranged from ?5.83 to 128.32 g C m^?2. The C input from litter decomposition was significant and must be quantified to accurately estimate NPP. Measuring C sequestration and NEP together may allow tracking of the effects of N addition on grassland C budgets. Overall, adding 25 or 10 g N m^?2 year^?1 improved the CO₂ sink of the grassland ecosystem, and increased grassland C sequestration.     

GIS-Based Emission Inventory, Dispersion Modeling, and Assessment for Source Contributions of Particulate Matter in an Urban Environment

The Industrial Source Complex Short Term (ISCST3) model was used to discern the sources responsible for high PM₁₀ levels in Kanpur City, a typical urban area in the Ganga basin, India. A systematic geographic information system-based emission inventory was developed for PM₁₀ in each of 85 grids of 2?×?2 km. The total emission of PM₁₀ was estimated at 11 t day^?1 with an overall breakup as follows: (a) industrial point sources, 2.9 t day^?1 (26%); (b) vehicles, 2.3 t day^?1 (21%); (c) domestic fuel burning, 2.1 t day^?1 (19%); (d) paved and unpaved road dust, 1.6 t day^?1 (15%); and the rest as other sources. To validate the ISCST3 model and to assess air-quality status, sampling was done in summer and winter at seven sampling sites for over 85 days; PM₁₀ levels were very high (89?C632 ??g m^?3). The results show that the model-predicted concentrations are in good agreement with observed values, and the model performance was found satisfactory. The validated model was run for each source on each day of sampling. The overall source contribution to ambient air pollution was as follows: vehicular traffic (16%), domestic fuel uses (16%), paved and unpaved road dust (14%), and industries (7%). Interestingly, the largest point source (coal-based power plant) did not contribute significantly to ambient air pollution. The reason might be due to release of pollutant at high stack height. The ISCST3 model was shown to produce source apportionment results like receptor modeling that could generate source apportionment results at any desired time and space resolution.     

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.     

The Nature and Distribution of Metals in Soils of the Sydney Estuary Catchment, Australia

Total topsoil 50th percentile Cu, Pb and Zn concentrations (n?=?491) in the Sydney estuary catchment were 23 ??g?g^?1, 60 ??g?g^?1 and 108 ??g?g^?1, respectively. Nine percent, 6% and 25% of samples were above soil quality guidelines, respectively and mean enrichment was 14, 35 and 29 times above background, respectively. Soils in the south-eastern region of the catchment exhibited highest metal concentrations. The close relationship between soil metal and road network distributions and outcomes of vehicular emissions modelling, strongly suggested vehicular traffic was the primary source of metals to catchment soils. Catchment soil and road dust probably make an important contribution to contamination of the adjacent estuary. The concentration of soil metals followed the land use trend: industrial?>?urban?>?undeveloped areas. A high proportion (mean 45%, 62% and 42%, for Cu, Pb and Zn, respectively) of metals in the soils may be bioavailable.     

Gaseous Elemental Mercury Fluxes in New York City

As with many urban environments, a number of sources of airborne elemental mercury (Hg°) exist in New York City, yet little research has been conducted to examine the flux and sources of mercury in New York. In this study, we conducted ambient monitoring of Hg° at six locations in New York City. Airborne Hg° averaged 3.84±0.10 ng m^-3 and 3.70±0.08 ng m^-3 in the boroughs of Manhattan and Brooklyn respectively, yet only 2.69±0.03 ng m^-3 in a more residential neighborhood in Queens. Both precipitation and ambient temperature were significantly correlated with ambient Hg° levels in New York City, suggesting that the surface emission of mercury from urban surfaces plays a role in urban Hg° concentrations. Local sources were also seen to contribute to urban Hg° levels by leading to `spikes' of Hg° in which elevated concentrations were recorded for short periods of time.     

Mercury in Biota and Surficial Sediments from Coatzacoalcos Estuary, Gulf of Mexico: Distribution and Seasonal Variation

Variation of mercury (Hg) in sediments and biota from Coatzacoalcos estuary during the dry, rainy and windy seasons was estimated. In sediments, Hg concentrations ranged from 0.07 μg g^?1 in site 13 (Ixhuatepec) located upstream, to 1.06 μg g^?1 in site 3 (Coatzacoalcos river), located in the industrialized area. Highest enrichment factor (EF) and index of geoaccumulation (I _geo) in surficial sediments were 53 and 5.1 respectively. From EF and I _geo, it is considered that Coatzacoalcos estuary is from moderately contaminated to contaminated. In most fish species from Coatzacoalcos estuary, the sequence of Hg concentration was liver>muscle>gills. Average Hg concentrations in soft tissue of bivalves ranged from 0.09 μg g^?1 in Corbicula fluminea to 0.18 μg g^?1 in Polymesoda caroliniana. Biota-sediment accumulation factor (BSAF) ranged from 0.9 in P. caroliniana during the rainy season (site 4) to 3.8 in P. caroliniana from the same site during the windy season.