Effect of soil on the mutagenic properties of waste water

The disposal of complex mixtures such as waste water on agricultural lands poses known and unknown environmental risks. Mutagens may be introduced into the eco-system and perhaps concentrated by crop plants or leached into ground water supplies. The purpose of this study was to determine the biological effect of a mutagenic waste water before and after application to soil. We used an XAD-8 methanol extract of waste water from the municipal sewage treatment facility at Sauget IL. This extract was a potent direct acting mutagen when assayed with the Salmonella typhimurium. 1 and 3 ml of extract were brought up to 10 ml volumes with water and added to 10 a of sterile or nonsterile , native clay loam. These mixtures were placed in a shaking water bath at room temperature for 0, 24, and 48 h. After separation of solid and liquid portions by filtration, dichloromethane was added to extract the organic fractions from each component. Solvent extractions were evaporated to dryness under vacuum and brought up in DMSO. Tests for mutagenic activity were conducted using strain TA98. After addition to the soil for greater periods of time the mutagenic activity decreased. The solid component exhibited greater mutagenic activity than the liquid. The XAD-8 extract was also assayed using the yg2 assay in Zea mays and the micronucleus assay in Tradescantia. The extract did not induce mutation or chromosome aberrations in these assays. The sludge from the Sauqet plant was chemically fractionated and assayed with S. typhimurium strains TA98 and TA100. The neutral fraction was the most mutagenic fraction followed by the weak acid,-strong acid and basic fractions. These chemical fractions uncovered more mutagenic potency than was predicted by assaying a crude organic extract of the sludge.U.S. Department of the InteriorU.S. Geological SurveyOpe

Advanced receptor modeling of near–real–time, ambient PM2.5 and its associated components collected at an urban–industrial site in Toronto, Ontario

AbstractPM2.5 and other atmospheric pollutants were continuously monitored at high time resolution for 1 year at an urban–industrial location in Toronto, ON, Canada's largest city. The data collected for these pollutants were examined to determine seasonal trends and potential sources. Advanced receptor models including residence time weighted concentration (RTWC) and simplified quantitative transport bias analysis (sQTBA) trajectory ensemble models (TEM) and conditional probability function (CPF) were applied to these data to identify potential local and regional sources of pollution impacting this receptor site. Seasonal trends showed that concentrations of PM2.5 were more frequently high in winter than in any other season. Median concentrations of lead and arsenic were highest in fall while median levels of chromium were not significantly different over the four seasons. The black carbon–derived measurement commonly known as Delta C (i.e., BC370nm–BC880nm) had its greatest abundance in winter and lowest levels in summer. The seasonality of Delta C is indicative of the impact of residential wood combustion near the receptor site. CPF indicated that lead and iron had the most unidirectional radial plots with sectors located west–southwest of the receptor being the most likely local source regions. Winter CPF for Delta C is almost of equal strengths in all directions suggestive of near–uniform isotropic local impacts. The sQTBA model provided the most satisfactory spatial representation of impacting sources. The strongest sources of PM2.5 identified by the sQTBA model were both local and transboundary in origin. More potential source regions were found in winter and summer than in spring and fall

Characterization of fine particulate sources at Ashaiman in Greater Accra, Ghana

AbstractThe sources of airborne fine particles in PM2.5 range influencing air quality at Ashaiman, a semi–urban town north of Tema in Ghana had been investigated. Nuclepore and quartz fiber filters were used for the air particulate loadings and analyzed for elemental and carbonaceous compound (EC and OC) concentrations in the 8 carbon fractions using X–Ray spectrometry system and IMPROVE/Thermal Optical Reflectance method respectively. Positive matrix factorization (PMF) was utilized to identify the following eight sources; industrial emissions (11.4%), fresh sea salt (15.5%), diesel emissions (18.4%), biomass burning (9.5%), two stroke engines (5.1%), gasoline emissions (15.8%), aged sea salt (6.2%), and soil dust (17.7%). Source locations were verified by means of Conditional Probability Function (CPF) plots that utilize wind directions. The source contributions revealed the high influence of fossil fuel and biomass combustion on the air quality in Ashaiman. The presence of the harbor and the industries located at Tema were seen to have substantial impacts on respirable air particulate matter (APM) concentrations in Ashaiman

Laboratory and Field Testing of an Automated Atmospheric Particle-Bound Reactive Oxygen Species Sampling-Analysis System

In this study, various laboratory and field tests were performed to develop an effective automated particle-bound ROS sampling-analysis system. The system uses 2′ 7′-dichlorofluorescin (DCFH) fluorescence method as a nonspecific, general indicator of the particle-bound ROS. A sharp-cut cyclone and a particle-into-liquid sampler (PILS) were used to collect PM2.5 atmospheric particles into slurry produced by a DCFH-HRP solution. The laboratory results show that the DCFH and H2O2 standard solutions could be kept at room temperature for at least three and eight days, respectively. The field test in Rochester, NY, shows that the average ROS concentration was 8.3 ± 2.2 nmol of equivalent H2O2 m−3 of air. The ROS concentrations were observed to be greater after foggy conditions. This study demonstrates the first practical automated sampling-analysis system to measure this ambient particle component

Particle nucleation in a forested environment

Peer reviewe

Urban air quality in a mid-size city — PM2.5 composition, sources and identification of impact areas: From local to long range contributions

Urban air quality represents a major public health burden and is a long-standing concern to European citizens. Combustion processes and traffic-related emissions represent the main primary particulate matter (PM) sources in urban areas. Other sources can also affect air quality (e.g., secondary aerosol, industrial) depending on the characteristics of the study area. Thus, the identification and the apportionment of all sources is of crucial importance to make effective corrective decisions within environmental policies. The aim of this study is to evaluate the impacts of different emissions sources on PM2.5 concentrations and compositions in a mid-size city in the Po Valley (Treviso, Italy). Data have been analyzed to highlight compositional differences (elements and major inorganic ions), to determine PM2.5 sources and their contributions, and to evaluate the influence of air mass movements. Non-parametric tests, positive matrix factorization (PMF), conditional bivariate probability function (CBPF), and concentration weighted trajectory (CWT) have been used in a multi-chemometrics approach to understand the areal-scale (proximate, local, long-range) where different sources act on PM2.5 levels and composition. Results identified three levels of scale from which the pollution arose: (i) a proximate local scale (close to the sampling site) for traffic non-exhaust and resuspended dust sources; (ii) a local urban scale (including both sampling site and areas close to them) for combustion and industrial; and (iii) a regional scale characterized by ammonium nitrate and ammonium sulfate. This approach and results can help to develop and adopt better air quality policy action

Hybrid multiple-site mass closure and source apportionment of PM2.5 and aerosol acidity at major cities in the Po Valley

This study investigates the major chemical components, particle-bound water content, acidity (pH), and major potential sources of PM2.5 in major cities (Belluno, Conegliano, Vicenza, Mestre, Padua, and Rovigo) in the eastern end of the Po Valley. The measured PM2.5 mass was reconstructed using a multiple-site hybrid chemical mass closure approach that also accounts for aerosol inorganic water content (AWC) estimated by the ISORROPIA-II model. Annually, organic matter accounted for 31-45% of the PM2.5 at all sites, followed by nitrate (10-19%), crustal material (10-14%), sulfate (8-10%), ammonium (5-9%), elemental carbon (4-7%), other inorganic ions (3-4%), and trace elements (0.2-0.3%). Water represented 7-10% of measured PM2.5. The ambient aerosol pH varied from 1.5 to 4.5 with lower values in summer (average in all sites 2.2±0.3) and higher in winter (3.9±0.3). Six major PM2.5 sources were quantitatively identified with multiple-site positive matrix factorization: secondary sulfate (34% of PM2.5), secondary nitrate (30%), biomass burning (17%), traffic (11%), re-suspended dust (5%), and fossil fuel combustion (3%). Biomass burning accounted for ∼90% of total PAHs. Inorganic aerosol acidity was driven primarily by secondary sulfate, fossil fuel combustion (decreasing pH), secondary nitrate, and biomass burning (increasing pH). Secondary nitrate was the primary driver of the inorganic AWC variability. A concentration-weighted trajectory (multiple-site) analysis was used to identify potential source areas for the various factors and modeled aerosol acidity. Eastern and Central Europe were the main source areas of secondary species. Less acidic aerosol was associated with air masses originating from Northern Europe owing to the elevated presence of the nitrate factor. More acidic particles were observed for air masses traversing the Po Valley and the Mediterranean, possibly due to the higher contributions of fossil fuel combustion factor and the loss of nitric acid due to its interaction with coarse sea-salt particles