An Analysis of Regional Haze Using Tracers of Opportunity

A two-year record of hourly concentrations of halocarbon tracers (methylchloroform and perchloroethylene) and hourly averages of particle light scattering (B_sp) has been analyzed In an effort to understand the sources of haze In the U.S. southwestern deserts and mountains. Measurements were taken on top of Spirit Mountain in southern Nevada. In conjunction with photographs used to interpret visual quality, haze episodes at Spirit Mountain were usually coincident with elevated concentrations of tracers originating from urban sources. Haze obscured an 88-km-distant mountain 17 percent of the total observation time. Of those Incidents, 69 percent were associated with long-range transport of haze from the Los Angeles Basin.     

The Coefficient of Haze as a Measure of Particulate Elemental Carbon

The technique to measure the coefficient of haze (COH) was developed in 1953 and was widely employed as a surrogate technique to measure total suspended particulate matter (TSP) in the 1960s. Because of the physical design of the sampler (known as the AISI Tape Sampler) used to measure COH, it was postulated that COH was directly related to the mass of fine elemental carbon particles (EC) with diameters less than 2.5 μm. To test the hypothesis, simultaneous samples of COH and EC were collected and analyzed during the 1981 Summer Study in Detroit. Regression analysis indicates that the two quantities are linearly related over the concentration range observed. Additional analyses indicate that COH is not related to TSP, fine particle mass, or light-scattering aerosol. Calculation of specific light absorption coefficients for EC from the COH data support the hypothesis that the tape sampler responds only to fine EC. A brief examination of historical COH data from Detroit suggests that the EC concentration has declined since 1972. This should be regarded as a preliminary assessment, however, until further verification of the COH-EC connection can be made.     

Causes of Haze in the Columbia River Gorge

Abstract

Visibility impairment in the Columbia River Gorge National Scenic Area is an area of concern. A field study conducted from July 2003 to February 2005 was followed by data analysis and receptor modeling to better understand the temporal and spatial patterns of haze and the sources contributing to the haze in the Columbia River Gorge in the states of Washington and Oregon. The nephelometer light scattering and surface meteorological data at eight sites along the gorge showed five distinct wind patterns, each with its characteristic diurnal and spatial patterns in light scattering by particles (b_sp). In summer, winds were nearly always from west to east (upgorge) and showed decreasing b_sp with distance into the gorge and a pronounced effect of the Portland, OR, metropolitan area on haze, especially in the western portions of the gorge. Winter often had winds from the east with very high levels of b_sp, especially at the eastern gorge sites, with sources east of the gorge responsible for much of the haze. The major chemical components responsible for haze were organic carbon, sulfate, and nitrate. Positive matrix factorization (PMF) using chemically speciated Inter-agency Monitoring of Protected Visual Environments data indicated seven source factors in the western gorge and five factors in the eastern gorge. Organic mass is a large contributor to haze in the gorge in all seasons, with a peak in fall. The PMF analysis suggests that approximately half of the organic mass is biomass smoke, with mobile sources as the second largest contributor. PMF analysis showed nitrates (important in fall and winter) mainly attributed to a generic secondary nitrate factor, with the next largest contributor being oil combustion at Mt. Zion, WA and mobile sources at Wishram, WA. Sulfate is a significant contributor in all seasons, with peak sulfate concentrations in summer.     

Haze is a risk factor contributing to the rapid spread of respiratory syncytial virus in children

This study investigated whether respiratory syncytial virus (RSV) infection in children was associated with ambient temperature and air pollutants in Hangzhou, China. A distributed lag non-linear model (DLNM) was used to estimate the effects of daily meteorological data and air pollutants on the incidence of RSV infection among children. A total of 3650 childhood RSV infection cases were included in the study. The highest air pollutant concentrations were in January to May and October to December during the year. The yearly RSV-positive rate was 10.0 % among children with an average age of 4.3 months. The highest RSV-positive rate occurred among patients 0 to 3 months old. Children under 6.5 months old accounted for 80 % of the total patients infected by RSV. A negative correlation was found between ambient temperature and RSV infection, and it was strongest with minimum ambient temperature (r = ?0.804, P < 0.001). There was a positive correlation between the infection rate and the particulate matter (PM) 2.5 (r = 0.446, P < 0.001), PM10 (r = 0.397, P < 0.001), SO₂ (r = 0.389, P < 0.001), NO₂ (r = 0.365, P < 0.001) and CO (r = 0.532, P < 0.001). The current study suggested that temperature was an important factor associated with RSV infection among children in Hangzhou. Air pollutants significantly increased the risk of RSV infection with dosage, lag and cumulative effects.     

Regional air pollution at a turning point

The control of transboundary air pollution in Europe has been successful. Emissions of many key pollutants are decreasing and there are signs of improvements in damaged ecosystems. The strategies under development within the CAFE programme under the European Commission and the Convention on Long-range Transboundary Air Pollution (CLRTAP), aim to take regional air pollution control a large step further, in particular with respect to small particles. In this paper we highlight the new strategies but look primarily at socioeconomic trends and climate change feedbacks that may have a significant influence on the outcome of the strategies and which so far have not been considered. In particular, we point out the influence on air quality of increased summer temperatures in Europe and of increasing emissions including international shipping, outside of Europe. Taken together the further emissions reductions in Europe and the increasing background pollution, slowly cause a greying of the Northern Hemisphere troposphere rather than the traditional picture of dominant emissions in Europe and North America ('black') with much lower emission intensities elsewhere ('white'). A hemispheric approach to further combat air pollution will become necessary in Europe and elsewhere.     

The Nature and Sources of Haze in the Shenandoah Valley/Blue Ridge Mountains Area

In order to investigate the nature and sources of regional haze, the General Motors mobile Atmospheric Research Laboratory was used in the summer of 1980 to monitor ambient air quality in the Shenandoah Valley of northern Virginia. On the average, 92% of the total light extinction was due to scattering by particles; the remainder was due to scattering by gases and absorption by gases and particles. Sulfate aerosols were the most Important visibility-reducing species. Averaging 55% of the fine participate mass, sulfates (and associated water) accounted for 78% of the total light extinction. The second most abundant fine particulate, accounting for 29% of the fine mass, was carbon—most of which was organic. Most of the remaining particulate mass and extinction were due to crustal materials. It is estimated that 78–86% of the total light extinction was caused by anthropogenic aerosol, most of which originated in major source areas of the midwest.     

PISCES: Tracking Trace Chemicals in Power Plants

PISCES, Power Plant Integrated Systems: Chemical Emissions Studies, is a multimedia chemical species project on plant emissions. Products generated in the PISCES project will help utilities design and operate their plants to minimize chemical species emissions. PISCES takes a holistic approach to the control of toxics by acknowledging that a chemical removed from a gas stream will appear in a liquid or solid stream.     

Tracking nitrogen losses in a greenhouse crop rotation experiment in North China using the EU-Rotate_N simulation model

Vegetable production in China is associated with high inputs of nitrogen, posing a risk of losses to the environment. Organic matter mineralisation is a considerable source of nitrogen (N) which is hard to quantify. In a two-year greenhouse cucumber experiment with different N treatments in North China, non-observed pathways of the N cycle were estimated using the EU-Rotate_N simulation model. EU-Rotate_N was calibrated against crop dry matter and soil moisture data to predict crop N uptake, soil mineral N contents, N mineralisation and N loss. Crop N uptake (Modelling Efficiencies (ME) between 0.80 and 0.92) and soil mineral N contents in different soil layers (ME between 0.24 and 0.74) were satisfactorily simulated by the model for all N treatments except for the traditional N management. The model predicted high N mineralisation rates and N leaching losses, suggesting that previously published estimates of N leaching for these production systems strongly underestimated the mineralisation of N from organic matter.     

Tracking the spectroscopic and chromatographic changes of algal derived organic matter in a microbial fuel cell

Changes in the characteristics of algae-derived organic matter (AOM) were examined upon the operation of a microbial fuel cell (MFC) using multiple analytical methods. Temporal variations in the UV absorption and fluorescence excitation–emission matrix of the AOM revealed that less condensed humic-like components and large-sized protein-like fluorescent compounds were preferentially decomposed over the period of electricity generation. They also showed that low UV-absorbing extracellular organic matters (EOM) were produced at the end of the operation. SEC chromatograms demonstrated that smaller-sized UV-absorbing components were initially decomposed, followed by the net production of EOM with an intermediate molecular weight. Fourier transform infrared (FT-IR) spectra showed that proteins and polysaccharides were the two most dominant structures of the AOM in the MFC. Two-dimensional correlation spectroscopy combined with FT-IR provided additional valuable information on the sequential changes of the AOM, which occurred in the order of proteins → acidic functional groups → polysaccharides → amino acids/proteins.     

Pollutant Transport During a Regional O3 Episode in the Mid-Atlantic States

ABSTRACT

Ozone (O₃) concentrations in the Baltimore-Washington (B-W) metropolitan area frequently exceed the National Ambient Air Quality Standard (NAAQS) in the summer months. The most extreme O₃ events occur in multi-day high O₃ episodes.¹ These events can be regional in scale, with O₃ concentrations exceeding the NAAQS at numerous locations along the eastern U.S. seaboard, and are typically associated with slow-moving or stagnant high pressure systems.^2-5 In the B-W region, the most extreme events typically occur with surface high pressure overhead or just west of the region and an upper air high-pressure area (ridge) to the west or northwest.¹ Besides providing conditions conducive to local O₃ production (subsidence and strong low-level inversions, weak horizontal winds, little cloud cover), this weather pattern may also result in transport of O₃ and its precursors from heavily industrialized areas west and north of the B-W region. In this paper, observations and back trajectories made during the severe regional O₃ event of July 12-15, 1995, are used to confirm the hypothesis that significant regional-scale transport of O₃ and its precursors occur during extreme O₃ events of the standard type in the B-W area.     

Statistical Issues in Assessing Anthropogenic Background for Arsenic

Conceptual and statistical issues surrounding the estimation of a background concentration distribution for arsenic are reviewed. How background area is defined and samples collected are shown to impact the shape and location of the probability density function that in turn affects the estimation and precision of associated distributional parameters. The overall background concentration distribution is conceptualized as a mixture of a natural background distribution, an anthropogenic background distribution and a distribution designed to accommodate the potential for contamination site samples being included into the background sample set. This concept is extended to a discussion of issues surrounding estimation of natural and anthropogenic background distributions for larger geographic areas. Finally, the mixture model is formally defined and statistical approaches to estimating its parameters discussed.     

Tracking chlordane compositional and chiral profiles in soil and vegetation

The cycling of chlordane and other persistent organic pollutants through the environment must be comprehensively elucidated to assess adequately the human health risks posed from such contaminants. In this study the compositional and chiral profiles of weathered chlordane residues in the soil and vegetative compartments were investigated in order to provide details of the fate and transport of this persistent pesticide. Zucchini was planted in a greenhouse in three bays containing chlordane-contaminated soil. At harvest the vegetation and soil were extracted and analyzed for chlordane content using chiral gas chromatography/ion trap mass spectrometry. Both achiral and chiral chlordane components were quantified. The chlordane concentration in the rhizosphere (soil attached to roots) was significantly less than that in the bulk soil. However, the enantiomeric ratio of the chiral components and overall component ratios had changed little in the rhizosphere relative to the bulk soil. Significant levels of chlordane were detected in the vegetation, the amount varying in different plant tissues from a maximum in roots to a minimum in fruit. In addition to the chlordane concentration gradient in plant tissues, significant shifts in compositional profile, as indicated by the component ratios, and in chiral profile, as indicated by the enantiomeric ratio, of the contaminant were observed in the plant tissues. The data indicate that abiotic processes dominate the transport of the chlordane components through the soil to the plant. This is the first report of the effect of rapid biotic processes within the plant compartment on chlordane compositional and chiral profiles.     

地下水曝气修复技术现场试验与应用研究进展

结合近年来国内外地下水曝气修复现场工程实践,对原位曝气的设计、操作和监测技术进行了全面的综述。对原位设计中的相关参数进行了整理分析,给出了合理取值范围,并探讨了不同场地条件下的应对方法。发展新的监测技术(如示踪技术、新型传感器等)能使曝气系统的工作性能得到更有效的监测,对于曝气修复工程现场监测新技术进行了系统的归纳和总结。此外,对现场曝气修复效果影响因素如污染物类型、曝气方式、曝气井数量、最大生物降解速率、土体孔隙率和含水层有机碳含量等进行了分析,以利于实际操作工艺的优化。最后对未来地下水曝气修复现场试验研究需开展的工作进行了展望。     

Regional contributions to airborne particulate matter in central California during a severe pollution episode

The externally-mixed source-oriented UCD/CIT air quality model was applied to determine the significance of inter-regional transport for primary and secondary particulate matter (PM) in California's Central Valley during a severe wintertime PM pollution episode from December 15, 2000 to January 7, 2001. The gases and primary PM emitted from eight different geographical sub-regions were tracked separately in a model simulation that included transport, physical and chemical transformation and deposition processes. The model results directly predict the contribution that each sub-region makes to PM concentrations throughout the entire model domain. The boundary layer was relatively stagnant during the simulated 3-week air quality episode, and no consistent transport pattern for primary PM was predicted. Several significant inter-regional transport events were identified that each lasted a few days. Each of these inter-regional events was characterized by transport of gas-phase precursors of nitrate that combined with local emissions of ammonia to produce particulate nitrate. Nitrate already in the particle phase was not transported efficiently due to higher dry deposition rates for particles relative to gas-phase nitrogen oxides. The distinctive pattern of transport for nitrate precursors reflects the relatively long timescales required to convert NO_x emissions to nitrate during winter conditions characterized by low temperatures, weak photolysis rates, and low oxidant concentrations. The equilibrium partitioning of nitrate and ammonia to the particle phase is relatively fast once the nitrate has been produced. The most-likely transport distance for nitrate during the current episode varied from 130–140 km for the northern portion of the Central Valley to 50–60 km in the southern portion of the Central Valley. Sub-regions further south in the Valley have smaller transport distances because of slower wind speeds and the greater abundance of ammonia in these areas, leading to faster conversion of gas-phase reactive nitrogen into particulate nitrate, which has a higher dry deposition rate than the gas-phase species. The most-likely transport distance for primary organic compounds (OC) was found to be less than that for nitrate, varying from 50 to 60 km for the northern portion of the Valley to 20–30 km for southern portion of the Valley. Overall, 68% of the particulate nitrate formed in the most polluted sub-regions of the Central Valley originates from emissions in those same sub-regions. Local emissions controls should therefore provide an effective strategy to reduce airborne particulate matter concentrations to acceptable levels.     

The Swedish Regional Climate Modelling Programme, SWECLIM: a review

The Swedish Regional Climate Modelling Programme, SWECLIM, was a 6.5-year national research network for regional climate modeling, regional climate change projections and hydrological impact assessment and information to a wide range of stakeholders. Most of the program activities focussed on the regional climate system of Northern Europe. This led to the establishment of an advanced, coupled atmosphere-ocean-hydrology regional climate model system, a suite of regional climate change projections and progress on relevant data and process studies. These were, in turn, used for information and educational purposes, as a starting point for impact analyses on different societal sectors and provided contributions also to international climate research.     

Organic composition of PM2.5 and size-segregated aerosols and their sources during the 2002 Bay Regional Atmospheric Chemistry Experiment (BRACE), Florida,USA

PM_2.5 and size-segregated aerosols were collected in May 2002 as part of the Bay Regional Atmospheric Chemistry Experiment (BRACE), Florida, USA. Aerosol organic composition was used to estimate sources of a series of alkanes and polycyclic aromatic hydrocarbons (PAHs) using chemical indices, hierarchical cluster analysis (HCA) and a chemical mass balance receptor model (CMB). Aerosols were collected on quartz fiber filters (QFF) using a PM_2.5 high volume sampler and on aluminum foil discs using a Micro-Orifice Uniform Deposit Impactor (MOUDI, 50% aerodynamic cut diameters were 18, 10, 5.6, 3.2, 1.8, 1.0, 0.56, 0.315 and 0.171 μm). Target compounds included alkanes and PAHs and were solvent extracted using a mixture of dichloromethane, acetone and hexane, concentrated and then analyzed using a gas chromatograph/mass spectrometer (GC/MS). The target compounds in PM_2.5 were dominated by six sources during the study period: mobile sources (39±5%), coal burning (33±5%), biogenic primary emission (20±2%), oil combustion (5±2%), biomass burning (1.0±0.3%) and an unidentified source (3±2%). Results obtained from the chemical indices, HCA and CMB were in very good agreement with each other. PAH size distributions are presented for days dominated by a same source. Seventy-five percent and 50% of the PAH were found below 1.8 and 0.56 μm, respectively (monthly PAH geometric diameters averaged 0.43 μm). Coarse size PAHs were observed on 1 day (15 May) and were correlated with nitrate and sodium size distribution. It is hypothesized that the PAHs, sodium and nitrate were internally mixed and that the PAHs deposited onto a pre-existing marine aerosol. This transfer process has significant implications for PAH deposition and lifetime and warrants further study.     

Regional differences of column-related aerosol parameters in Germany

With the development of satellite experiments supplementary and validating ground-based measurements are gaining growing importance for the inference and evaluation of radiation-related aerosol parameters. Both kinds of measurements have been conducted and interpreted mainly under globally or locally restricted aspects for a limited time period only. Results are presented from four rural regions (coastal zone, lowlands, highlands, high mountain); they are column-related aerosol parameters, deduced from monitoring programs of spectral aerosol optical depth (AOD) as well as almucantar sky irradiance measurements. After 13 years of continuous measurements of trends and variations in aerosol optical depths, these results are based on 5 years of data collection (1994–1998). There are significant differences among the parameters of the four regions when related to the inversion method of the AOD spectra. A clear interdependence was found between all column-related parameters and the real part of the refractive index, which in turn depends on the chosen retrieval method. The differences among the four regions are characterized mainly by their different altitudes, with relative humidity being responsible for their internal variation. An increase in the relative humidity from 35 to 55–60% influences the most interesting parameters such as refractive index (real part), hemispheric backscattered fraction b, and direct radiative forcing ΔF as follows: The real part of the refractive index decreases from 1.6±0.05 to 1.42±0.04, b decreases by 8–10%, and, due to the increase in AOD, ΔF increases by about 20% in the spectral region 0.4–1.0 μm. The quantities of the parameters depend on the retrieval methods too.