Background levels of air and precipitation quality for Europe

This paper is intended to be used by specialists engaged in air and precipitation quality management on regional and continental scales. Major goals are to establish definition, methodology and specific values of background air and precipitation quality for sulfur (S) and nitrogen (N) species to be used in practical applications of air resources management. Major findings are the following:

• 1.(a) 69% of SO₂ and 63 % of NO₂ concentration over Europe originate from continental scale anthropogenic sources,
• 2.(b) 15% of precipitation sulfate and 11% of precipitation nitrate over Europe are contributed by hemispheric background,
• 3.(c) hemispheric background pollution values for Europe were found as 1.25 μg (SO₂-S)m⁻³, 0.80 μg (SO₄²⁻-S)m⁻³, 0.157 mg (SO₄²⁻-S)l⁻¹ and 0.04 mg (NO₃⁻-N)ℓ⁻¹.

     

Inter-storm comparisons from the OSCAR high density network experiment

The high density network component of the Oxidation and Scavenging Characteristics of April Rains (OSCAR) experiment combined aircraft, surface and sequential precipitation chemistry measurements to characterize the physicochemical and dynamic features of four storms sampled during an April 1981 field investigation. A surface network of 47 precipitation sampling stations, covering a region roughly 110 km by 110 km, was established in the area surrounding Fort Wayne, Indiana. The network provided temporal and spatial resolution of rainfall chemistry via the use of specially designed automatic sequential bulk precipitation collectors, while aircraft and surface sampling provided measurements of the major aerosols and trace gases in the boundary-layer inflow region.Composite concentration and ion ratio profiles for the events were analyzed to investigate potential pollutant scavenging pathways. This analysis led to the following observations:

• 1.(i) dryfall deposition during pre-rainfall exposure periods influenced initial sampler stage chemistry;
• 2.(ii) relative precipitation acidity increased throughout the events; SO₄²⁻ and NO₃⁻ were the major contributors to this acidity;
• 3.(iii) evidence exists for the in-cloud oxidation of SO₂ during Events 3 and 4, while scavenging of HNO₃ and aerosol NO₃⁻ probably produced precipitation NO₃⁻;
• 4.(iv) the non-frontal meteorology of Event 3 influenced the precipitation chemistry associated with this storm and led to distinct concentration profiles;
• 5.(v) an anomalous pattern of NH₄⁺ concentrations observed during Event 1 cannot be explained by known NH₄⁺ scavenging behavior or by non-scavenging related influences, such as local source contamination or NH₃ volatilization;
• 6.(vi) Event 4 is more suitable for analysis by one- and two-dimensional diagnostic wet removal models. Analysis of the other events is complicated by more complex meteorological behavior and, in some cases, a less complete chemistry data set. This paper enlarges on these observations with comparisons of the major meteorological and chemical characteristics of the four events.

     

Results from the Total Exposure Assessment Methodology (TEAM) study in selected communities in Northern and Southern California

Volatile organic compound levels (VOCs) in breath, personal air, fixed outdoor air and drinking water samples were measured and compared for a probability sample of individuals in Los Angeles and Antioch/Pittsburg, California during 1984. In addition, comparisons were made between seasons (winter vs spring) in Los Angeles for individuals sampled in both seasons. The statistics presented to compare the sites and seasons were primarily percent measurable and concentration levels (e.g. sample medians). For most comparisons, 13 VOC levels were examined for breath, personal and outdoor air samples and four VOCs for water samples.In addition to the results for VOC levels, the paper also briefly describes

• 1.(i) the sampling procedures used to obtain the study participants
• 2.(ii) the collection of air, breath and water samples
• 3.(iii) selected results from the quality assurance procedures used in this study.

For most chemicals, the percent measurable and concentration levels were

• 1.(i) higher in personal air samples than in breath or outdoor air samples,
• 2.(ii) higher in Los Angeles in the winter for air and breath than in the, spring,
• 3.(iii) higher in Los Angeles for air and breath than in Antioch/Pittsburg,
• 4.(iv) quite different for water as compared with air and breath.

Ubiquitous compounds in water were chloroform, bromodichloromethane, dibromochloromethane and bromoform while in air and breath they were 1,1,1-trichloroethane, benzene, tetrachloroethylene, ethylbenzene and the xylenes.Concentrations were higher in

• 1.(i) outdoor air vs breath in the winter in Los Angeles (where outdoor air levels were much higher than in the spring),
• 2.(ii) in personal air vs outdoor air in the upper tails of the concentration distribution (90th percentile) compared to the 50th percentile. For the water samples, relatively high concentrations were noted for chloroform, bromodichloromethane and dibromochloromethane.

In most cases, water concentrations were higher for Los Angeles in the spring. Five VOCs known to be in tobacco smoke (benzene, styrene, ethylbenzene and the xylenes) had significantly higher levels in the breath of smokers.     

Report on a British Council specialist tour to India

This Report describes a tour from 2 to 14 January 1986 in Delhi and New Delhi. The principal objectives were:

• 1.(1) To participate in the Indian Science Congress Meeting.
• 2.(2) To present a paper in the section on ‘Recent advances in numerical modelling of the disperion of atmospheric pollutants’ and make an appraisal of the value of the meeting and suggestions for future meetings.
• 3.(3) Discuss the research programme of the Centre for Advanced Studies in Atmospheric and Fluid Sciences of the Indian Institute of Technology with staff and research students and make recommendations for the future direction and development of this programme.
• 4.(4) Participate in seminars and discussions at the Centre. A general impression of the Indian air pollution scene is also given, and its relationship to past and present situations in other parts of the world is discussed.

     

Inherent uncertainty in air quality modeling

This paper summarizes the discussions of a working group that was charged with the task of examining inherent uncertainty in air quality modeling. The major topics of the paper are:

• 1.1. Definition of inherent uncertainty in air quality models;
• 2.2. Determination of inherent uncertainty;
• 3.3. Role of inherent uncertainty in model evaluation.

The concepts introduced here are illustrated through a numerical simulation with Gifford's fluctuating plume model.     

Co-occurrence patterns of gaseous air pollutant pairs at different minimum concentrations in the United States

The frequency of co-occurrences for SO₂NO₂, SO₂/O₃ and O₃/NO₂ at rural and remote monitoring sites in the United States was characterized for the months of May-September for the years 1978–1982. Minimum hourly concentrations of 0.03 and 0.05 ppm of each gas were used as the criteria for defining a ‘co-occurrence’. The objectives of this study were to:

• 1.(1) identify the types of co-occurrence patterns and their frequency;
• 2.(2) identify whether the frequency of hourly simultaneous co-occurrences increased substantially when the minimum concentration was lowered (e.g. from 0.05 to 0.03 ppm) for each pollutant; and
• 3.(3) determine whether the frequency of co-occurrences showed large year-to-year variation.

For all pollutant pairs and co-occurrence thresholds (i.e. 0.03 and 0.05 ppm), the frequency of daily and hourly co-occurrences was low for most sites. Year-to-year variability was found to be insignificant; most of the monitoring sites experienced co-occurrences of any type less than 12% of the 153 days. Based on our observations, researchers attempting to assess the potential effects of SO₂/NO₂, SO₂/O₃ and O₃/NO₂ in the United States should construct simulated exposure regimes so that

• 1.(1) hourly simultaneous and daily simultaneous-only co-occurrences are fairly rare and
• 2.(2) when co-occurrences are present, complex-sequential and sequential-only co-occurrence patterns predominate.

     

On the nature of nitrate particles in a coastal urban area

Application of micro spot and electron microscopy techniques to individual particles in a coastal urban site revealed the following:

• 1.(a) sulfate particles, some of them mixed, dominated the sub-μm (0.3–0.8 μm) size range;
• 2.(b) nitrates were found mostly in the μm size range, in the form of NaNO₃.

The latter was verified by X-ray analysis of individual nitrates. Apparently the NaNO₃ particles were formed through heterogeneous reaction of gaseous HNO₃ with sea salt particles.     

Continuous four-dimensional source attribution for the Berlin area during two days in July 1994. Part II: Sensitivity studies

The multiple nested three-dimensional (3D) mesoscale Eulerian grid point model MM5 is directly coupled with a Lagrangian particle trajectory model in order to perform a four-dimensional source attribution for the area of Berlin based on the horizontal distribution of the import probability density (IPD). The technical aspects are already demonstrated in the companion paper A (Part I) including the illustration of the meteorological situation at the two consecutive days of investigation and a primarily 3D source attribution. We conducted further sensitivity studies concerning the effect of vertical mixing, the static stability of the particles/emissions and the regarded time scale on the IPD distribution which is extended to four dimensions. The main results are:

• •Heterogeneity and temporal variability of the wind field enhance the contributions of nearby sources (emissions) to the total import of the receptor in contrast to stationary wind fields which increase the scope of the IPD distribution in the upstream direction.
• •Regions of static stability, for example morning hour inversion layers, enhance the contribution of far distance sources with longer import times.
• •The import velocities increase, as far as long distance source-receptor transitions are concerned, because they are mostly realised via higher transport paths.
• •The third (vertical) dimension is not negligible for the task of a complete source attribution, as a considerable amount of elevated emissions, preferably out of 300±100 m elevation, reaches the receptor box which is only 50 m in depth. Hence, downward mixing of elevated and far distance sources is an important process and driven by the diurnal course of turbulence and low level jets within the PBL
• •On the short time scale (few days), the source attribution is not independent from the regarded time scale (simulation time) due to the neglecting of older emissions released before the beginning of the simulation.

     

Nitration of gaseous polycyclic aromatic hydrocarbons in simulated and ambient urban atmospheres: A source of mutagenic nitroarenes

Recent results from field studies in the Los Angeles air basin which focused on the nature and concentrations of mononitroarenes in the gaseous and particulate states in polluted ambient air are reviewed. Relative concentrations in organic extracts of ambient particulate polycyclic organic matter (POM) were found to be, in decreasing order, 2-NO₂-fluoranthene > 1-NO₂-pyrene ≳ 2-NO₂-pyrene; this is in sharp contrast to primary emissions of diesel soot, where 1-NO₂-PY > 3-NO₂-FL > 8-NO₂-FL. Since light and heavy duty diesel motor vehicle emissions are a significant source of sub-μm particles in the Los Angeles area, the relatively high abundance of 2-NO₂-FL suggests that a significant fraction of the 2-NO₂-FL in southern California may be formed via atmospheric reactions. In a wintertime 1986 study of a high-NO_x episode ~ 20 km east of the Los Angeles International Airport, high concentrations of 1- and 2-nitronaphthalenes, much of which could have been in the gaseous state, were collected on a polyurethane backup ‘plug,’ along with lesser amounts of 2-NO₂-FL (and 1- and 2-NO₂-PY) adsorbed on the particles collected by a Hi-vol prefilter.Two gas phase mechanisms are proposed for the formation of adsorbed 2-NO₂-fluoranthene and gaseous 2-NO₂-naphthalene in urban air

• 1.(a) during daylight, attack on gaseous FL by OH radicals followed by NO₂ addition, loss of H₂O and condensation of 2-NO₂-FL on particle surfaces
• 2.(b) reaction with N₂O₅ at night under ambient conditions during which the gaseous NO₃ radical and NO₂ are present, in equilibrium with N₂O₅. Chamber experiments with simulated polluted atmospheres support both of these mechanisms for the formation of 2-NO₂-FL and 2-NO₂-naphthalene; only the OH mechanism seems valid for 2-NO₂-PY. Environmental and health implications of these studies are briefly discussed.

     

Evaluation of environmental impact produced by different economic activities with the global pollution index

Introduction

The paper analyses the environment pollution state in different case studies of economic activities (i.e. co-generation electric and thermal power production, iron profile manufacturing, cement processing, waste landfilling, and wood furniture manufacturing), evaluating mainly the environmental cumulative impacts (e.g. cumulative impact against the health of the environment and different life forms).

Materials and methods

The status of the environment (air, water resources, soil, and noise) is analysed with respect to discharges such as gaseous discharges in the air, final effluents discharged in natural receiving basins or sewerage system, and discharges onto the soil together with the principal pollutants expressed by different environmental indicators corresponding to each specific productive activity. The alternative methodology of global pollution index (I _GP ^* ) for quantification of environmental impacts is applied.

Results and discussion

Environmental data analysis permits the identification of potential impact, prediction of significant impact, and evaluation of cumulative impact on a commensurate scale by evaluation scores (ES_i) for discharge quality, and global effect to the environment pollution state by calculation of the global pollution index (I _GP ^* ).

Conclusions

The I _GP ^* values for each productive unit (i.e. 1.664?C2.414) correspond to an ??environment modified by industrial/economic activity within admissible limits, having potential of generating discomfort effects??. The evaluation results are significant in view of future development of each productive unit and sustain the economic production in terms of environment protection with respect to a preventive environment protection scheme and continuous measures of pollution control.     

Bioconcentration of superlipophilic persistent chemicals

According to present understanding, persistent superlipophilic chemicals — such as octachlorodibenzo-p-dioxin, octachlorodibenzofuran, Mirex etc — with log K_ow > 6 and cross sections > 9.5 Å, bioconcentrate in aquatic organisms only little from ambient water. The most convincing argument against it is that in bioconcentration experiments with superlipophilic chemicals amounts applied exceeded water solubility by several orders of magnitude. This paper describes various methods for determining bioconcentration factors (BCF) of superlipophilic compounds. As exemplified with octachlorodibenzo-p-dioxin, BCF values evaluated by these methods match well with those calculated by QSARs for fish and mussels based on log K_ow and water solubility. As expected, these BCF values exceed previous values by several orders of magnitude. For BCF evaluation of superlipophilic chemicals in aquatic organisms we recommend:

1. flow-through systems, kinetic method (OECD guideline No. 305 E)
2. ambient concentrations < water solubility
3. during the uptake and especially during the elimination phase no toxic effects of the test organisms should occur.

     

Erratum to “Continuous four-dimensional source attribution for the Berlin area during two days in July 1994. Part I: The new Euler–Lagrange-model system LaMM5”: [Atmospheric Environment 35 (32) (2001) 5497]

The multiple nested three-dimensional (3D) mesoscale Eulerian grid point model MM5 was directly coupled with a Lagrangian particle trajectory model in order to perform a 4D source attribution for the area of Berlin based on the import probability density (IPD) distribution of the according receptor box. Within the resulting model system LaMM5 introduced here, the IPD distributions are not based on backward trajectories, which lack the recognition of the turbulent environment, but on the forward integration of a huge amount (order of million per day) of particle releases according to an emission scenario which is approximately continuous in space and time. Hence, the receptor import yields an accordingly continuous IPD distribution. Much attention has been paid on spatial and temporal resolution at the interface between both model parts (online-coupling) and the interface itself has been extended by the turbulent quantities resulting from the higher-order turbulence closure of the Eulerian model part. LaMM5 is applied on an episode with high photochemical activity across Berlin at two consecutive days (25 and 26 July 1994) with varying meteorological conditions leading to an accordingly different source attribution. The main results are:

• •The decay of the Berlin IPD with increasing source-receptor distance and time appears in an exponential manner if only sources out of a constant level (z=25 m) are regarded.
• •Heterogeneous wind fields in time and space enhance the contributions (emissions) of nearby sources to the total import of the receptor in contrast to stationary wind fields which increase the scope of the IPD distribution in upstream direction.

There are further results from several additional sensitivity studies presented in a companion paper B (Part II).     

Continuous four-dimensional source attribution for the Berlin area during two days in July 1994. Part I: the new Euler–Lagrange-model system LaMM5

The multiple nested three-dimensional mesoscale Eulerian grid point model MM5 was directly coupled with a Lagrangian particle trajectory model in order to perform a four-dimensional source attribution for the area of Berlin based on the import probability density (IPD) distribution of the according receptor box. Within the resulting model system LaMM5 introduced here, the IPD distributions are not based on backward trajectories, which lack the recognition of the turbulent environment, but on the forward integration of a huge amount (order of Million per day) of particle releases according to an emission scenario which is approximately continuous in space and time. Hence the receptor import record yields an accordingly continuous IPD distribution. Much attention has been paid on spatial and temporal resolution at the interface between both model parts (online-coupling) and the interface itself has been extended by the turbulent quantities resulting from the higher-order turbulence closure of the Eulerian model part. LaMM5 is applied on an episode with high photochemical activity across Berlin at two consecutive days (25th and 26th of July in 1994) with varying meteorological conditions leading to an accordingly different source attribution. The main results are:

• •The decay of the Berlin IPD with increasing source-receptor distance and time appears in an exponential manner if only sources out of a constant level (z=25 m) are regarded.
• •Heterogeneous wind fields in time and space enhance the contributions (emissions) of nearby sources to the total import of the receptor in contrast to stationary wind fields which increase the scope of the IPD distribution in upstream direction.

There are further results from several additional sensitivity studies presented in a companion paper B (Part II).     

Gaseous nitrogen losses from a forest site in the North Tyrolean Limestone Alps

Microorganisms are responsible for the mineralisation of organic nitrogen in soils. NH ⁺₄ can be further oxidised to NO₃ ⁻ during nitrification and NO₃ ⁻ can be reduced to gaseous nitrogen compounds during denitrification. During both processes, nitrous oxide (N₂O), which is known as greenhouse gas, can be lost from the ecosystem.

The aim of this study was to quantify N₂O emissions and the internal microbial N cycle including net N mineralisation and net nitrification in a montane forest ecosystem in the North Tyrolean Limestone Alps during an 18-month measurement period and to estimate the importance of these fluxes in comparison with other components of the N cycle. Gas samples were taken every 2 weeks using the closed chamber method. Additionally, CO₂ emission rates were measured to estimate soil respiration activity. Net mineralisation and net nitrification rates were determined by the buried bag method every month. Ion exchange resin bags were used to determine the N availability in the root zone.

Mean N₂O emission rate was 0.9 kg N ha⁻a⁻, which corresponds to 5 % of the N deposited in the forest ecosystem. The main influencing factors were air and soil temperature and NO ⁻₃ accumulated on the ion exchange resin bags. In the course of net ammonification, 14 kg NH ⁺₄ −N ha⁻ were produced per year. About the same amount of NO ⁻₃ −N was formed during nitrification, indicating a rather complete nitrification going on at the site. NO ^t-₃ concentrations found on the ion exchange resin bags were about 3 times as high as NO ^t-₃ produced during net nitrification, indicating substantial NO ^t-₃ immobilisation. The results of this study indicate significant nitrification activities taking place at the Mühleggerköpfl.

     

Contaminants of food

A scheme has been developed to rank 70 industrial organic chemicals in order of their priority for further study as potential contaminants of food. Numerical scales were developed for the following seven key criteria concerning environmental issues, food and toxicity:

-Production volume

-Pattern of usage

-Possible fate in the environment

-Likelihood of chemical entering the food chain

-Mechanism of entry into the food chain

-Persistence and accumulation in the food chain

-Toxicity.

Each chemical was assigned a score for the above criteria, which were combined to give an overall ranking for the chemicals. This scheme has been endorsed by the MAFF Steering Group on Chemical Aspects of Food Surveillance. It will be used in the assessment of relative priorities for further non-statutory surveillance for these contaminants in the UK food supply.     

Optimization of nitrate reduction by EDTA catalyzed zero-valent bimetallic nanoparticles in aqueous medium

The present study aims to investigate the EDTA catalyzed reduction of nitrate (NO ₃ ^? ) by zero-valent bimetallic (Fe?CAg) nanoparticles (ZVBMNPs) in aqueous medium and to enumerate the effect of temperature, solution pH, ZVBMNPs dose and EDTA concentration on NO ₃ ^? reduction. Batch experimental data were generated using a four-factor Box?CBehnken design. Optimization modeling was performed using the response surface method for maximizing the reduction of NO ₃ ^? by ZVBMNPs. Significance of the independent variables and their interactions were tested by the analysis of variance and t test statistics. The model predicted maximum reduction capacity (340.15?mg?g^?1 NO ₃ ^? ) under the optimum conditions of temperature, 60?°C; pH?4; dose, 1.0?g?l^?1; and EDTA concentration, 2.0?mmol?l^?1 was very close to the experimental value (338.62?mg?g^?1) and about 16?% higher than the experimentally determined capacity (291.32?mg?g^?1). Study demonstrated that ZVBMNPs had higher reduction efficiency than Fe⁰ nanoparticles for NO ₃ ^? . EDTA significantly enhanced the NO ₃ ^? reduction by ZVBMNPs. The EDTA catalyzed reduction of NO ₃ ^? by ZVBMNPs can be employed for the effective decontamination of water.     

Microbial structure and chemical components of aerosols caused by rotating brushes in a wastewater treatment plant

Purpose

Bacterial community structure and the chemical components in aerosols caused by rotating brushes in an Orbal oxidation ditch were assessed in a Beijing municipal wastewater treatment plant.

Methods

Air samples were collected at different distances from the aerosol-generating rotating brushes. Molecular culture-independent methods were used to characterize the community structure of the airborne bacteria in each sample regardless of cell culturability. A clone library of 16S rDNA directly amplified from air DNA of each sample was constructed and sequenced to analyze the community composition and diversity. Insoluble particles and water-soluble ions emitted with microorganisms in aerosols were analysis by a scanning electron microscope together with energy dispersive X-ray spectroscopy and ion chromatogram analyzer.

Results

In total, most of the identified bacteria were Proteobacteria. The majority of sequences near the rotating brushes (the main source of the bioaerosols) were Proteobacteria (62.97 %) with ??-(18.52 %) and ??-(44.45?%) subgroups and Bacteroidetes (29.63 %). Complex patterns were observed for each sampling location, suggesting a highly diverse community structure, comparable to that found in water in the Orbal oxidation ditch. Accompany with microorganisms, 46.36???g/m³ of SO ₄ ^2? , 29.35???g/m³ of Cl^?, 21.51???g/m³ of NO ₃ ^? , 19.76???g/m³ of NH ₄ ⁺ , 11.42???g/m³ of PO ₄ ^3? , 6.18???g/m³ of NO ₂ ^? , and elements of Mg, Cl, K, Na, Fe, S, and P were detected from the air near the aerosols source.

Conclusions

Differences in the structure of the bacterial communities and chemical components in the aerosols observed between sampling sites indicated important site-related variability. The composition of microorganisms in water was one of the most important sources of bacterial communities in bioaerosols. Chemical components in bioaerosols may provide a media for airborne microorganism attachment, as well as a suitable microenvironment for their growth and survival in the air. This study will be benefit for the formulation of pollution standards, especially for aerosols, that take into account plant workers?? health.     

Removal ratio of gaseous toluene and xylene transported from air to root zone via the stem by indoor plants

This work was designed to investigate the removal efficiency as well as the ratios of toluene and xylene transported from air to root zone via the stem and by direct diffusion from the air into the medium. Indoor plants (Schefflera actinophylla and Ficus benghalensis) were placed in a sealed test chamber. Shoot or root zone were sealed with a Teflon bag, and gaseous toluene and xylene were exposed. Removal efficiency of toluene and total xylene (m, p, o) was 13.3 and 7.0 μg·m^?3·m^?2 leaf area over a 24-h period in S. actinophylla, and was 13.0 and 7.3 μg·m^?3·m^?2 leaf area in F. benghalensis. Gaseous toluene and xylene in a chamber were absorbed through leaf and transported via the stem, and finally reached to root zone, and also transported by direct diffusion from the air into the medium. Toluene and xylene transported via the stem was decreased with time after exposure. Xylene transported via the stem was higher than that by direct diffusion from the air into the medium over a 24-h period. The ratios of toluene transported via the stem versus direct diffusion from the air into the medium were 46.3 and 53.7 % in S. actinophylla, and 46.9 and 53.1 % in F. benghalensis, for an average of 47 and 53 % for both species. The ratios of m,p-xylene transported over 3 to 9 h via the stem versus direct diffusion from the air into the medium was 58.5 and 41.5 % in S. actinophylla, and 60.7 and 39.3 % in F. benghalensis, for an average of 60 and 40 % for both species, whereas the ratios of o-xylene transported via the stem versus direct diffusion from the air into the medium were 61 and 39 %. Both S. actinophylla and F. benghalensis removed toluene and xylene from the air. The ratios of toluene and xylene transported from air to root zone via the stem were 47 and 60 %, respectively. This result suggests that root zone is a significant contributor to gaseous toluene and xylene removal, and transported via the stem plays an important role in this process.     

Characteristics of precipitation chemistry at Lushan Mountain, East China: 1992–2009

Introduction

Trends in precipitation pH and conductivity during 1992?C2009, and in ionic compositions from January 2007 to June 2009, are reported from Lushan Mountain, one of the highest mountains in mid-east China. Annual mean pH was in the range of 4.35?C5.01 and showed a statistically very significant (P?P?Results and discussions Over the period of study, Lushan Mountain received more rainfall in spring and summer. The pH values varied seasonally with winter minima. The winter multiyear seasonal mean pH was 4.35. The corresponding summer value was 4.88. SO ₄ ^2? and NO ₃ ^? were the main anions, and NH ₄ ⁺ and Ca²⁺ the main cations. The anion to cation ratio was 0.8?C1.0, and that of [SO ₄ ^2? ] to [NO ₃ ^? ] was 2.4-3.0, much lower than that of the 1980s. However, sulfuric acid was still the main acid present. The ratio of [NH ₄ ⁺ ] to [Ca²⁺] was about 1.0, suggesting that these two alkaline substances provided close acid neutralizing capacity. The ratio of [Cl^?] to [Na⁺] was about 0.67, somewhat lower than that of natural precipitation.

Conclusions

Ionic composition varied seasonally and was closely correlated to the amounts of rainfall and pollution. Trajectory analyses showed that the trajectories to Lushan Mountain could be classified in six clusters and trajectories originating from the South Sea and the areas surrounding Lushan Mountain had the greatest impacts on precipitation chemistry.     

Characterization of PM10 atmospheric aerosol at urban and urban background sites in Fuzhou city, China

Background

PM₁₀ aerosol samples were simultaneously collected at two urban and one urban background sites in Fuzhou city during two sampling campaigns in summer and winter. PM₁₀ mass concentrations and chemical compositions were determined.

Methods

Water-soluble inorganic ions (Cl^?, NO ₃ ^? , SO ₄ ^2? , NH ₄ ⁺ , K⁺, Na⁺, Ca²⁺, and Mg²⁺), carbonaceous species (elemental carbon and organic carbon), and elements (Al, Si, Mg, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, and Pb) were detected using ion chromatography, thermal/optical reflectance, and proton-induced X-ray emission methods, respectively.

Results

PM₁₀ mass concentrations, as well as most of the chemical components, were significantly increased from urban background to urban sites, which were due to enhanced anthropogenic activities in urban areas. Elements, carbonaceous species, and most of the ions were more uniformly distributed at different types of sites in winter, whereas secondary ion SO ₄ ^2? , NO ₃ ^? , and NH ₄ ⁺ showed more evident urban-background contrast in this season. The chemical mass closure indicated that mineral dust, organic matters, and sulfate were the most abundant components in PM₁₀. The sum of individually measured components accounted for 86.9?C97.7% of the total measured PM₁₀ concentration, and the discrepancy was larger in urban area than in urban background area.

Conclusion

According to the principal component analysis?Cmultivariate linear regression model, mineral dust, secondary inorganic ions, sea salt, and motor vehicle were mainly responsible for the PM₁₀ particles in Fuzhou atmosphere, and contributed 19.9%, 53.3%, 21.3%, and 5.5% of PM₁₀, respectively.