Indoor Polycyclic Aromatic Hydrocarbon Concentration in Central India

The indoor burning of different materials like fuels, incense, mosquito coil, candles etc. results in generation of polycyclic aromatic hydrocarbons (PAHs) in an uncontrolled manner. The PAH, i.e., Benzo(a)pyrene (BaP) is considered as most toxic or carcinogenic and the toxicity of other PAHs is related to this compound. Therefore, the concentration and emission fluxes of polycyclic aromatic hydrocarbons (PAHs) emitted during burning of commonly used indoor materials, i.e., 15 fuels (i.e., biomass (BM), coal (C), cow dung (CD), kerosene (K)), 4 incense (IS) and mosquito coil (MC) in Raipur district, Chhattisgarh, central India is described. The samples were taken in September 2013 in indoor environments and respective smoke emitted were collected using high volume United State of America (USA) air sampler on quartz fiber filters. The concentration of total 13 PAHs (∑PAH₁₃) (i.e., phenanthrene, anthracene, fluoranthene, pyrene, benz(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)-pyrene, dibenz(ah)anthracene, benzo(ghi) perylene, indeno1,2,3-(cd)pyrene, and coronene) in particulate matter (PM₁₀) in the indoor air during burning of the fuels, IS and MC materials ranged from 367–92052 ng m^?3, 4089–14047 ng m^?3, and 66–103 ng m^?3 with mean values of 7767 ± 11809 ng m^?3, 9977 ± 4137 ng m^?3, and 74 ± 20 ng m^?3, respectively. The mean concentration of the ∑PAH₁₃ present in indoor environment is much higher than the WHO limit value of 1.0 ng m^?3. The sources and toxicities of PAHs are discussed.     

Source Allocation of Aliphatic and Polycyclic Aromatic Hydrocarbons in Particulate-Phase (PM10) in the City of Valdivia,Chile

The concentration and signature of n-alkanes (n-C₁₀ to n-C₃₃) and 18 PAHs were determined in air filters across a year period (2010) in an urban area of the city of Valdivia, Chile. Filter samples were extracted using sohxlet apparatus and analyzed by GC-MS techniques. Concentrations of total hydrocarbons ranged from 45–352 ng.m^?3 and total PAHs ranged from 2.93–78.01 ng.m^?3. Concentrations of hydrocarbons during the summer were high (288–352 ng.m^-3) and reduced when the autumn began (45–79 ng.m^?3) to then increase almost linearly to the next summer. The drop in concentration was attributed in part to the significant reduction of traffic when summer ends as tourists leave the city (about 9–15% of the total cars circulating). Results from the chemometric technique of Polytopic Vector Analysis (PVA) indicated three main sources for the alkanes: biogenic (terrestrial plants), signatures of oil combustion, and an unconfirmed source which is thought to come from non specific organic matter degradation. Total PAHs correlated well with total particulate matter with a R² = 0.94. Levels of PAHs in the atmosphere were higher during the winter (6.85–78.01 ng.m^?3) period than the rest of the year (2.93–36.30 ng.m^?3). PVA results indicate three key sources of PAHs and two of those sources derived from oil combustion and biomass burning.     

Analysis of Aerosolized Particulates of Feedyards Located in the Southern High Plains of Texas

The objective of this study was to quantify, size, and examine the composition of particulates found in ambient aerosolized dust of four large feedyards in the Southern High Plains. Ambient air samples (concentration of dust) were collected upwind (background) and downwind of the feedyards. Aerosolized particulate samples were collected using high volume sequential reference ambient air samplers, PM ₁₀ and PM _2.5 , laser strategic aerosol monitors, cyclone air samplers, and biological cascade impactors. Weather parameters were monitored at each feedyard. The overall (main effects and estimable interactions) statistical (P < 0.0001) general linear model statement (GLM) for PM ₁₀ data showed more concentration of dust (μg/m ³ of air) downwind than upwind and more concentration of dust in the summer than in the winter. PM _2.5 concentrations of dust were comparable for 3 of 4 feedyards upwind and downwind, and PM _2.5 concentrations of dust were lower in the winter than in the summer. GLM (P < 0.0001) data for cascade impactor (all aerobic bacteria, Enterococcus spp, and fungi) mean respirable and non-respirable colony forming units (CFU) were 676 ± 74 CFU/m ³ , and 880 ± 119 CFU/m ³ , respectively. The PM ₁₀ geometric mean size (±GSD) of particles were analyzed in aerosols of the feedyards (range 1.782 ± 1.7 μm to 2.02 ± 1.74μm) and PM _2.5 geometric mean size particles were determined (range 0.66 ± 1.76 μm to 0.71 ± 1.71 μm). Three of 4 feedyards were non-compliant for the Environmental Protection Agency (EPA) concentration standard (150 μg/m ³ /24 h) for PM ₁₀ particles. This may be significant because excess dust may have a negative impact on respiratory disease.     

Seasonal and Spatial Variation of Polycyclic Aromatic Hydrocarbons in Vapor-Phase and PM2.5 in Southern California Urban and Rural Communities

Fifteen priority polycyclic aromatic hydrocarbons (PAHs) were measured in two rural communities (Atascadero and Lompoc) located several hundred km northwest of Los Angeles and in four urban communities 40–100 km downwind of Los Angeles (San Dimas, Upland, Mira Loma, and Riverside), during all seasons, from May 2001 to July 2002. PM_2.5 and vapor-phase PAHs were collected, on prebaked quartz fiber filters and PUF-XAD-4 resin, respectively, at 113 LPM, during 24 h periods, every eighth day, and quantified by HPLC-Fluorescence. At all sites vapor-phase PAHs contained > 99.9% of the total PAH mass and were dominated by naphthalene (NAP), which varied from about 60 ng m ^{? 3} in Lompoc, a community with light traffic, to ～580 ng m ^{? 3} in Riverside, a community traversed by ～200,000 vehicles day^{? 1}. During summer pollution episodes in urban sites, NAP concentrations reached 7–30 times annual averages. Except for summer episodes, concentrations of low MW PAHs showed small seasonal variations (～2 times higher in winter). Similar concentrations of particle-phase PAHs were observed at all sites except for Lompoc. Benzo[ghi]perylene (BGP), a marker of gasoline exhaust emissions, showed the highest concentration among particle-phase PAHs, varying from 23.3 pg m^?3 in Lompoc to 193 pg m^?3 in Mira Loma. Benzo[a]pyrene and indeno[1,2,3-cd]pyrene, found exclusively in the particle phase, were much higher in urban sites (～40–100 pg m^?3), than in Lompoc (～12 pg m^?3). Winter particle-phase PAHs were 2 to 14 times higher than summer levels. Particle-phase PAHs were negatively correlated with mean air temperature in urban sites (r = ?0.50 to ?0.75), probably resulting from surface inversions occurring during winter. The data suggest that in Southern California vehicular exhaust emissions are a major contributor to particle-phase PAHs.     

Chemical Characteristics of Fine Particles (PM1) from Xi'an,China

Daily mass concentrations of water-soluble inorganic (WS-i) ions, organic carbon (OC), and elemental carbon (EC) were determined for fine particulate matter (PM₁, particles < 1.0 μm in diameter) collected at Xi'an, China. The annual mean PM₁ mass concentration was 127.3 ± 62.1 μg m^–3: WS-i ions accounted for ～38% of the PM₁ mass; carbonaceous aerosol was ～30%; and an unidentified fraction, probably mostly mineral dust, was ～32%. WS-i ions and carbonaceous aerosol were the dominant species in winter and autumn, whereas the unidentified fraction had stronger influences in spring and summer. Ion balance calculations indicate that PM₁ was more acidic than PM_2.5 from the same site. PM₁ mass, sulfate and nitrate concentrations followed the order winter > spring > autumn > summer, but OC and EC levels were higher in autumn than spring. Annual mean OC and EC concentrations were 21.0 ± 12.0 μg m^?3 and 5.1 ± 2.7 μg m^–3 with high OC/EC ratios, presumably reflecting emissions from coal combustion and biomass burning. Secondary organic carbon, estimated from the minimum OC/EC ratios, comprised 28.9% of the OC. Positive matrix factorization (PMF) analysis indicates that secondary aerosol and combustion emissions were the major sources for PM₁.     

Performance of wearable ionization air cleaners: Ozone emission and particle removal

Wearable ionization air cleaners are compact in size and marketed for personal respiratory protection by removing air pollutants from users' breathing zone. In this study, ozone emission and particle removal rates of four wearable ionization air cleaners (namely, AC1 through AC4) were evaluated inside a 0.46 m³ stainless steel chamber. Continuous measurements were conducted for ozone concentration, PM_2.5 concentration, and particle size distribution in the size range of 18.1–289 nm. Two of the four wearable air cleaners (i.e., AC1 and AC2) had detectable ozone emissions. The 10-h average ozone emission rates were quite different (i.e., 0.67 mg·h^?1 for AC1 and 3.40 × 10^?2 mg·h^?1 for AC2); however, the ozone emissions were negligible for AC3 and AC4. The number removal rates for particles within the measured size range were highly variable (i.e., 2.20 h^?1, 0.52 h^?1, 8.10 h^?1, and 27.9 h^?1 for AC1 through AC4, respectively). The corresponding mass removal rates of PM_2.5 were 1.85 h^?1, 0.48 h^?1_,1.52 h^?1, and 5.37 h^?1, respectively. Regulatory guidelines are needed to assure these devices can effectively remove particles without ozone emissions to protect public health.

Copyright © 2016 American Association for Aerosol Research     

Chemically Resolved Particle Fluxes Over Tropical and Temperate Forests

Chemically resolved submicron (PM₁) particle mass fluxes were measured by eddy covariance with a high resolution time-of-flight aerosol mass spectrometer over temperate and tropical forests during the BEARPEX-07 and AMAZE-08 campaigns. Fluxes during AMAZE-08 were small and close to the detection limit (<1 ng m^?2 s^?1) due to low particle mass concentrations (<1 μg m^?3). During BEARPEX-07, concentrations were five times larger, with mean mid-day deposition fluxes of ?4.8 ng m^?2 s^?1 for total nonrefractory PM₁ (V_ex,PM1 = ?1 mm s^?1) and emission fluxes of +2.6 ng m^?2 s^?1 for organic PM₁ (V_ex,org = +1 mm s^?1). Biosphere–atmosphere fluxes of different chemical components are affected by in-canopy chemistry, vertical gradients in gas-particle partitioning due to canopy temperature gradients, emission of primary biological aerosol particles, and wet and dry deposition. As a result of these competing processes, individual chemical components had fluxes of varying magnitude and direction during both campaigns. Oxygenated organic components representing regionally aged aerosol deposited, while components of fresh secondary organic aerosol (SOA) emitted. During BEARPEX-07, rapid in-canopy oxidation caused rapid SOA growth on the timescale of biosphere-atmosphere exchange. In-canopy SOA mass yields were 0.5–4%. During AMAZE-08, the net organic aerosol flux was influenced by deposition, in-canopy SOA formation, and thermal shifts in gas-particle partitioning. Wet deposition was estimated to be an order of magnitude larger than dry deposition during AMAZE-08. Small shifts in organic aerosol concentrations from anthropogenic sources such as urban pollution or biomass burning alters the balance between flux terms. The semivolatile nature of the Amazonian organic aerosol suggests a feedback in which warmer temperatures will partition SOA to the gas-phase, reducing their light scattering and thus potential to cool the region.

Copyright 2013 American Association for Aerosol Research     

Humidity,density, and inlet aspiration efficiency correction improve accuracy of a low-cost sensor during field calibration at a suburban site in the North-Western Indo-Gangetic plain (NW-IGP)

Abstract

Low-cost particulate matter (PM) sensors are now widely used by concerned citizens to monitor PM exposure despite poor validation under field conditions. Here, we report the field calibration of a modified version of the Laser Egg (LE), against Class III US EPA Federal Equivalent Method PM₁₀ and PM_2.5 β-attenuation analyzers. The calibration was performed at a site in the north-western Indo-Gangetic Plain from 27 April 2016 to 25 July 2016. At ambient PM mass loadings ranging from <1–838?µg m^?3 and <1–228?µg m^?3 for PM₁₀ and PM_2.5, respectively, measurements of PM₁₀, PM_2.5 from the LE were precise, with a Pearson correlation coefficient (r) >0.9 and a percentage coefficient of variance (CV) <12%. The original Mean Bias Error (MBE) of ～?90?µg m^?3 decreased to ?30.9?µg m^?3 (Sensor 1) and ?23.2?µg m^?3 (Sensor 2) during the summer period (27 April–15 June 2016) after correcting for particle density and aspiration losses. During the monsoon period (16 June–25 July 2016) the MBE of the PM_2.5 measurements decreased from 19.1?µg m^?3 to 8.7?µg m^?3 and from 28.3?µg m^?3 to 16.5?µg m^?3 for Sensor 1 and Sensor 2, respectively, after correcting for particle density and hygroscopic growth. The corrections reduced the overall MBE to <20?µg m^?3 for PM₁₀ and <3?µg m^?3 for PM_2.5, indicating that modified version of the LE could be used for ambient PM monitoring with appropriate correction and meteorological observations. However, users of the original product may underestimate their PM₁₀ exposure.

Copyright © 2020 American Association for Aerosol Research     

ALIPHATIC,POLYCYCLIC AROMATIC HYDROCARBONS AND NITRATED-POLYCYCLIC AROMATIC HYDROCARBONS IN PM 10 IN SOUTHWESTERN MEXICO CITY

A sampling campaign of airborne particles ≤ 10 μ m (PM ₁₀ ) was carried out from February to April of 2004 at the Universidad Nacional Autónoma de México in southwestern Mexico City. The average PM ₁₀ mass concentration was 51 ± 14 μ g m^?3. Extracted organic matter was determined, with a mean of 6.5 ± 1.7 μ g m^?3, which represents 12.9% of PM ₁₀ mass concentration. The standard additions method was used on real samples at four concentration levels for 13 n-alkanes, 14 PAHs and 5 nitro-PAHs. The average concentration for the sum was 99.04 ng m^{? 3} for n-alkanes, 4.9 ng m^?3 for PAHs and 710 pg m^{? 3} for nitro-PAHs. Higher concentrations of n-alkanes > C ₂₄ were found, indicating biogenic emissions as the dominant source. Coronene, benzo[ghi]perylene, benzo[b+j+k]fluoranthenes and indeno[1,2,3-cd]pyrene were the most abundant PAHs, suggesting a strong contribution from incomplete combustion of gasoline. The PAHs considered for calculating BaPE represented 52% of the total PAHs analyzed. The presence of 9-nitroanthracene indicates direct emission from diesel combustion and heterogeneous nitrating reactions on sorbed particles, while 2-nitrofluoranthene, indicates gas-phase reactions with fluoranthene, hydroxyl (OH^?) and/or nitrate (NO ₃ ^?) radicals in the presence of nitrogen oxides (NOx).     

Development and application of a simultaneous measurement method for gaseous ammonia and particulate ammonium in ambient air

Ammonia gas is one of the precursors contributing to the formation of secondary particulate ammonium via reactions with atmospheric acids, such as sulfuric and/or nitric acids, which are present in ambient air. In this study, a new instrument that is suitable for measuring ammonia gas and fine particulate ammonium (PM_2.5 NH₄⁺) concentrations simultaneously under ambient conditions was developed. A wetted frit sampler was connected in the back of a counter-current flow tube (CCFT) sampler, and the NH₃ gas and PM_2.5 NH₄⁺ samples were collected by CCFT and wetted frit samplers, respectively. An air sample was drawn through the samplers at a flow rate of 1.0 dm³ min^?1 and an absorption water flow rate of 120 mm³ min^?1. Then, the ammonium that formed in the absorption solution was detected by the indophenol method using a continuous flow analysis system. The estimated detection limits were 43 and 49 ng m^?3 for ammonia gas and PM_2.5 NH₄⁺, respectively. Notably, the ammonia gas was collected on the CCFT sampler with a collection efficiency of 98.5%, but most of the PM_2.5 NH₄⁺ passed through it and was captured on the wetted frit sampler with a collection efficiency of approximately 100%. The present method was applied to measure NH₃ gas and PM_2.5 NH₄⁺ at two urban sites: Osaka, Japan and Ho Chi Minh City, Vietnam. It was found that the simultaneous measurement method performed very well and that the measured concentrations were comparable with those obtained with the annular denuder method.

Copyright © 2016 American Association for Aerosol Research     

Chronic pulmonary exposure to traffic-related fine particulate matter causes brain impairment in adult rats

Background

Effects of air pollution on neurotoxicity and behavioral alterations have been reported. The objective of this study was to investigate the pathophysiology caused by particulate matter (PM) in the brain. We examined the effects of traffic-related particulate matter with an aerodynamic diameter of <?1 μm (PM₁), high-efficiency particulate air (HEPA)-filtered air, and clean air on the brain structure, behavioral changes, brainwaves, and bioreactivity of the brain (cortex, cerebellum, and hippocampus), olfactory bulb, and serum after 3 and 6 months of whole-body exposure in 6-month-old Sprague Dawley rats.

Results

The rats were exposed to 16.3?±?8.2 (4.7~?68.8) μg/m³ of PM₁ during the study period. An MRI analysis showed that whole-brain and hippocampal volumes increased with 3 and 6 months of PM₁ exposure. A short-term memory deficiency occurred with 3 months of exposure to PM₁ as determined by a novel object recognition (NOR) task, but there were no significant changes in motor functions. There were no changes in frequency bands or multiscale entropy of brainwaves. Exposure to 3 months of PM₁ increased 8-isoporstance in the cortex, cerebellum, and hippocampus as well as hippocampal inflammation (interleukin (IL)-6), but not in the olfactory bulb. Systemic CCL11 (at 3 and 6 months) and IL-4 (at 6 months) increased after PM₁ exposure. Light chain 3 (LC3) expression increased in the hippocampus after 6 months of exposure. Spongiosis and neuronal shrinkage were observed in the cortex, cerebellum, and hippocampus (neuronal shrinkage) after exposure to air pollution. Additionally, microabscesses were observed in the cortex after 6 months of PM₁ exposure.

Conclusions

Our study first observed cerebral edema and brain impairment in adult rats after chronic exposure to traffic-related air pollution.

     

Emissions of CH4, N2O, NH3 and odorants from pig slurry during winter and summer storage

Manure storage contributes significantly to greenhouse gas (GHG), NH₃ and odour emissions from intensive livestock production. A pilot-scale facility with eight 6.5-m³ slurry storage units was used to quantify emissions of CH₄, N₂O, NH₃, and odorants from pig slurry during winter and summer storage. Pig slurry was stored with or without a straw crust, and with or without interception of precipitation, i.e., four treatments, in two randomized blocks. Emissions of total reduced S (mainly H₂S) and p-cresol, but not skatole, were reduced by the straw crust. Total GHG emissions were 0.01–0.02 kg CO₂ eq m^?3 day^?1 during a 45-day winter storage, and 1.1–1.3 kg CO₂ eq m^?3 day^?1 during a 58-day summer storage period independent of storage conditions; the GHG balance was dominated by CH₄ emissions. Nitrous oxide emissions occurred only during summer storage where, apparently, emissions were related to the water balance of the surface crust. An N₂O emission factor for slurry storage with a straw crust was estimated at 0.002–0.004. There was no evidence for a reduction of CH₄ emissions with a crust. Current Intergovernmental Panel on Climate Change recommendations for N₂O and CH₄ emission factors are discussed.     

Fine particles sampled at an urban background site and an industrialized coastal site in Northern France—Part 2: Comparison of offline and online analyses for carbonaceous aerosols

Particulate matter was sampled in Northern France during two summer and winter periods at both an urban background site (Douai, DO) and an industrialized coastal site (Grande-Synthe, GS). Ambient levels of particulate carbonaceous species and Polycyclic Aromatic Hydrocarbons (PAH) were measured by real-time measurements and via collection and analysis of offline filters (F). The comparison between online organic matter (OM) measured by an Aerosol Mass Spectrometer (AMS) and organic carbon (OC) determined by an offline thermal-optical method showed good linear trends in wintertime GS (r² = 0.82 while only 0.50 in summer), and DO (r² = 0.86 in summer and 0.92 in winter). However, significant differences were observed between analytical methods and sites with OC_AMS/OC_F ratios decreasing from 0.80 in DO during winter to ≈0.20 for GS in summer, suggesting that a large part of OM could be in the PM₁–PM_2.5 fraction. The simultaneous measurements of Black Carbon (BC) and Elemental Carbon (EC) concentrations in PM_2.5 were also well correlated at both sites with r² = 0.61–0.97 and slopes between 0.6 and 0.8. PAHs were analyzed in PM_2.5 and also measured online by AMS in PM₁. Their wintertime concentrations were highly correlated in DO (r² = 0.98) and to a lesser degree in GS (r² = 0.67). r² values determined for comparison between online and offline parameters (OC and PAHs) in GS were lower than in DO, probably due to a more complex aerosol composition and a higher variability of the physical and chemical properties resulting from the coastal situation and diversity of emission sources in the vicinity of GS.

Copyright © 2018 American Association for Aerosol Research     

Personal Exposure of Children to Particle-Associated Polycyclic Aromatic Hydrocarbons in Tianjin,China

Polycyclic aromatic hydrocarbons (PAHs) associated with fine particles are harmful to human health, particularly to children, who are most vulnerable. To evaluate the respiratory exposure of children to particle-associated PAHs properly, personal air sampling near breathing zone of 36 schoolchildren were conducted in Tianjin, China. Sixteen priority PAHs designated by the United States Environmental Protection Agency were measured using GC-MS. The average concentrations of personal exposure to ∑₁₆PAH were 27.31 ± 3.91 ng/m³ in summer and 58.18 ± 24.68 ng/m³ in winter. Moreover, PAH profiles were studied and the results showed NAP, BbF, and IPY were the most abundant PAHs. Five rings PAH species made up the largest proportion, accounting for 25.7% in summer and 32.6% in winter. Diagnostic ratios and principal component analysis indicated combustion activities were the major source for children exposure to particle-associated PAHs in this study. According to the risk assessment results, the inhalation exposure risk for children were higher than the acceptable risk level of 10–⁶, indicating the health issues of children should be paid more attention. On the basis of sensitivity analysis results, further research should be done to improve the inhalation cancer slope factor of BaP and the concentration distribution of PAHs in order to improve the accuracy of the health risk assessment.     

Characteristics of secondhand electronic cigarette aerosols from active human use

The electronic cigarette (EC) is a new source of indoor airborne particles. To better understand the impacts of secondhand vaping (SHV) emissions on indoor air quality, real-time measurements of particle size distribution, particle number concentration (PNC), fine particulate matter (PM_2.5), CO₂, CO, and formaldehyde were conducted before, during, and after 10 min EC-use among 13 experienced users in an 80 m³ room. To assess particle transport in the room, multiple sampling locations were set up at 0.8, 1.5, 2.0, and 2.5 m away from the subjects. The arithmetic mean (standard deviation) of background PNC and PM_2.5 concentrations in the room were 6.39 × 10³ (1.58 × 10²) particles/cm³ and 8 (1) μg/m³, respectively. At 0.8 m away from EC users, right after initiation of puffing, the PNC and PM_2.5 concentrations can reach a peak of ～10⁵ particles/cm³ and ～3 × 10³ µg/m³, respectively, and then dropped quickly to background levels within 20 s due to dilution and evaporation. At the 0.8 m sampling location, the mean PNC and PM_2.5 concentrations during puffing were 2.48 × 10⁴ (2.14 × 10⁴) particles/cm³ and 188 (433) µg/m³, respectively. In addition, two modes of SHV particles were observed at about 15 and 85 nm. Moreover, concentrations of SHV particles were negatively correlated with the distances to EC users. At the 1.5 m location, PNC and PM_2.5 levels were 9.91 × 10³ (1.76 × 10³) particles/cm³ and 19 (14) µg/m³, respectively. Large variations of mean PNC levels exhaled per puff were observed both within and between EC users. Data presented in this study can be used for SHV particle exposure assessment.

Copyright © 2017 American Association for Aerosol Research     

Associations of Fungal Aerosols,Air Pollutants,and Meteorological Factors

The relationships between fungal aerosols and air pollutants meteorological factors were investigated in the Taipei urban area. In summer, it was observed that geometric mean (GM) concentrations of airborne fungal aerosols were 2,835 CFU m^-3 and 2,651 CFU m^-3 at Kuting and Hsichih stations, respectively. In winter, GM levels of airborne fungi were 1,107 CFU m I 3 and 2,248 CFU m^-3 at Kuting and Hsichih stations, respectively. Moreover, fungal aerosol concentrations were observed to highly depend on weather conditions, and the highest concentration of total colony counts appeared when the temperature was 25-30 C, the RH was 60-70% , and the wind speed was > 1 m s^-1 and from the S-SE wind direction. In addition, total fungal concentrations were negatively correlated with ozone concentrations, and concentration of Cladosporium spp. was positively correlated with hydrocarbons. PM₁₀ were positively correlated with Penicillium and the yeasts in Hsichih station. Our results demonstrated that airborne fungal aerosols are definitely correlated with air pollutants and meteoro logical factors. The complex dynamic interactions were indicated to occur among bioaerosols, air pollutants, and meteorological factors.     

Analysis of Polycyclic Aromatic Hydrocarbon,Toxic Equivalency Factor and Related Carcinogenic Potencies in Roadside Soil within a Developing City of Northern India

Preliminary analysis was performed to assess contamination levels in roadside soils, distribution behavior and human exposure with Polycyclic Aromatic Hydrocarbons (PAHs) during summer, winter, rainy, and autumn during 2013 in one of the developing cities of northern India. The concentration of PAHs was measured at ten different locations (at 1, 2, and 3 m) from roadside soil. Recovery range was 30% and 80% with lower value corresponding to the lower molecular weight PAHs compound. Identification and quantification of PAHs was done by GC-FID. Average PAHs concentration (city average) was found to be 16.53, 4.04, 17.49, and 7.82 μg g^?1, during summer, winter, autumn, and the rainy seasons, respectively. Average concentration of low and high carcinogenic PAHs during summer, winter, autumn, and rainy was 5.1 and 31.29, 2.1 and 6.4, 4.74 and 35.08, 3.97 and 12.77μg g^?1_, respectively. The average ratio of low and high carcinogenic PAHs was found to be 1:6, 1:3, 1:7.6, and 1:3.21 during summer, winter, autumn, and the rainy seasons at most intercepts. Dib(ah)A and B(a)P were the two individual PAHs found in highest concentration during summer, winter, and the rainy seasons, whereas B(a)P and IP were individual PAHs found in highest concentration during autumn. It was also analyzed that high carcinogenic PAHs concentration was quite higher (around 85%) in comparison to low carcinogenic PAHs (around 15%) at most intercepts. This article also deals with the behavior of PAHs at places of average/high population and traffic density intercepts. Five-ringed PAHs were in highest concentration at all intercepts and seasons. Two-tailed T test was applied for authenticity of the data and results. Toxic equivalency factor of B(a)P and Dib(ah)A was maximum as compared to other PAHs.     

Determination of Averaged Long-term Air Concentrations of Semivolatile Polycyclic Aromatic Hydrocarbons: First Results

Abstract

Using our long-term sampling methodology presented previously, consecutive 14-day air samples of semivolatile polycyclic aromatic hydrocarbons (PAH) (from fluoranthene/pyrene to coronene) were collected over the time-span of nearly a whole year at a semi-rural site (Jülich) and quantified by GC-FID. As expected, concentrations were higher in winter [3 ng m^?3 for benzo[e]pyrene (BEP)] than in summer (0.4 ng m^?3 for BEP). However, normalized concentrations (to BEP =1) showed constant values for most PAH; thus, a largely stable PAH profile is obvious. Exceptions are benzo[a]pyrene and benz[a]anthracene: their concentrations normalized to BEP were lower in summer, indicating specific losses. Reasons for these losses are unknown as yet, although degradation reactions during atmospheric transport are a distinct possibility.     

Composition and Source Apportionment of Organic Aerosol in Beirut,Lebanon, During Winter 2012

Fine organic aerosols were collected at a semi-urban site in Beirut, Lebanon, from 28 January to 12 February 2012 as part of the Emission and Chemistry of Organic Carbon in East Mediterranean-Beirut (ECOCEM-Beirut). A total of 20 quartz filter samples were collected on a 12 h basis using a high-volume sampler and were analyzed using a GC/MS technique. Levoglucosan was the major most abundant single component with an average value of 306 ng.m^?3, followed by saturated and unsaturated carboxylic acids and sugars with average values of 234 and 118 ng.m^?3, respectively. Reported values for other carboxylic acids, polycyclic aromatic hydrocarbons, and biogenic secondary organic aerosols (BSOA) were 87, 33 and 21 ng.m^?3, respectively. Compared to a similar field campaign conducted in summer 2011, levoglucosan concentrations were lower in summer by a factor of 6, due to the use of wood burning for residential heating in winter. Concentrations of saturated and unsaturated carboxylic acids, other carboxylic acids, and BSOA were higher in summer by a factor of 3, 2, and 7, respectively. Higher concentrations observed for BSOA and other dicarboxylic acids during summer are due to higher biogenic emissions and greater photochemical activity in summer.

Copyright 2013 American Association for Aerosol Research