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PREFACE

Special Issue of Aerosol Science and Technology for Air Pollution and Health: Bridging the Gap from Sources-to-Health Outcomes

Pages i-vii | Published online: 04 Jul 2011

THE CONFERENCE

The U.S. Environmental Protection Agency (EPA) has established National Ambient Air Quality Standards (NAAQS) for six principal air pollutants (“criteria” pollutants): carbon monoxide (CO), lead (Pb), nitrogen dioxide (NO2), particulate matter (PM) in two size ranges (<2.5 μm [PM2.5] and <10 μm [PM10]), ozone (O3), and sulfur dioxide (SO2) (U.S. EPA Citation2010a). Although associations have been identified between these pollutants and adverse health effects, considerable uncertainty remains regarding (a) methods and approaches to understanding relationships between air pollution and health effects; (b) which components (gas and/or particles) and sources are most toxic; (c) the mechanisms of actions of the pollutants and causal relationships; (d) effect of confounding factors, and (e) which populations are susceptible (U.S. EPA Citation2006a [Pb], 2006b [O3], 2008a [NOx Integrated Science Assessment [ISA]], 2008b [SOx ISA], 2009 [PM ISA], 2010b [CO]). This holds true especially for PM, because it is composed of many components with significant spatial and temporal variations (Solomon et al. Citation2008; U.S. EPA Citation2009). Air pollution and health research continues to reduce these uncertainties across the source-to-health effects paradigm as described by the National Research Council (NRC) Research Priorities for Airborne Particulate Matter, volumes I–IV, (NRC 1998, 1999, 2001, 2004) and the U.S. EPA (Citation2006a, 2006b, 2008a, 2008b, 2009, 2010b).

Linking air pollution and adverse health effects is complicated and requires expertise across a range of scientific disciplines—from atmospheric to exposure to health sciences, as well as inclusion of air quality managers and policy makers who implement and develop policy to reduce risk from air pollution. Interaction among these groups at different points in time helps to identify gaps in knowledge and suggest future research directions. One such opportunity was the international specialty conference “Air Pollution and Health: Bridging the Gap from Sources to Health Outcomes,” sponsored by the American Association for Aerosol Research (AAAR 2010). The conference, chaired by myself and Maria Costantini (Health Effects Institute), was designed to help disseminate and integrate results from scientific studies that cut across the range of air pollution and health-related disciplines of the source-to-health effects continuum. Conference objectives are listed in . The conference addressed the science of air pollution and health within a multipollutant framework, focusing on five key science areas—sources, atmospheric sciences, exposure, dose, and health effects—as identified by the NRC (1998). Eight key policy-relevant science questions that integrated across various parts of these science areas formed the basis of the meeting, and a ninth question addressed the policy implications of the findings ().

TABLE 1 Conference objectives

TABLE 2 Science questions

This was the AAAR's third international specialty conference and extended the findings presented at the AAAR's first specialty conference “Particulate Matter: Atmospheric Sciences, Exposure, and the Fourth Colloquium on PM and Human Health,” held in Pittsburgh, Pennsylvania, in 2003 (Davidson et al. 2005).

Results from the 2010 AAAR Air Pollution and Health conference are being published in Aerosol Science and Technology (AS&T); Environmental Health Perspectives (Solomon Citation2011 ); Air Quality, Atmosphere and Health; Atmospheric Environment; and Inhalation Toxicology (Solomon Citation2010).

THIS ISSUE

This special issue of Aerosol Science and Technology includes selected papers from the Air Pollution and Health Conference that align with the goals and objectives of Aerosol Science and Technology. Study objectives described in each paper align with the conference science questions as indicated in . Key findings also are presented in with brief project descriptions given below.

The first three papers in this issue, characterize different emissions sources, one located outdoors and two located indoors. Cahill et al. (Citation2011a) examined emissions from the Roseville Rail Yard located in Sacramento, CA. Roseville is the largest rail yard on the west coast of the United States and a previous study indicated an increase in cancer risk for the neighborhood downwind of the rail yard. Aerosol samples were collected in up to 9 size ranges for five weeks in the summer and fall of 2005 and analyzed for mass, optical absorption, and trace elements at a time resolution of 3 h. Organic species were obtained separately but only during the night. Data were collected simultaneously upwind and downwind of the rail yard and the difference was estimated as the emissions contribution of the rail yard to ambient downwind concentrations. Hourly measurements of NO, NO2, and black carbon (BC) were obtained from a collaborating study. Diesel exhaust from the trains, indicated by the observed difference in chemistry from up- versus downwind measurements primarily impacted ultrafine (UF, <100 nm) and very fine (90–260 nm) particles. Heavy PAH species, at a higher proportion than observed from diesel truck emissions also were observed in the UF size range. Anthropogenic-derived metals and petroleum-derived n-alkanes showed enrichment in the coarse particles.

Indoor sources examined included cooking and emissions of nanoparticles from a laser printer. Wang et al. (Citation2011) measured nanoparticle emissions directly from the page output area of a laser printer and characterized these emissions for volatile organic carbon (VOC), particle number concentration, size distribution, morphology, elements, and positive and negative ion concentrations, the latter determined with an ion density meter. Similar physical and chemical properties were determined for the toner material as well. Toner usage per page was based on iron content of the toner material compared to that determined on a given page. Maximum nanoparticle emissions were observed when the internal surfaces of the printer were cold at the beginning of printing and also depended on the number of printed pages and age of the generated aerosol. Strategies to reduce emissions were described. Buonanno et al. (Citation2011) examined the volatile fraction of cooking-generated particles by measuring the size distribution and number concentration of the emitted particles as a function of thermal conditioning. Emissions testing including several fat rich foods (cheese, pork meat, bacon) and vegetables (eggplants, onions, chips) cooked by both grilling and frying. Both categories of food contained fractions of volatile material that was measured by a shift in the size distribution to a smaller size mode. Results indicated that particles emitted when cooking vegetables had a higher fraction of volatile material as compared to cooking fatty foods, the latter explained by the presence of a solid core likely due to the partial synthesis and degradation of fatty acids to aldehydes and ketones.

TABLE 3 Relationship of special issue paper objectives to conference science questions (SQ) as given in

The next two papers in this issue characterize outdoor and/or indoor aerosols. Wheeler et al. (Citation2011) obtained continuous measurements of fine particle (<2.5 μm) mass, BC, and UF particles over 5 days in the winter and in summer and at both indoor and outdoor residences of 48 adults in 2005 and 47 asthmatic children in 2006. Air exchange rates also were measured. Diurnal and seasonal variations were examined along with indoor/outdoor ratios. Outdoor concentrations of the pollutants measured were higher than indoor with nighttime minimums and peaks around morning rush hour, indicating motor vehicles as an important morning source of pollution. Indoor/outdoor ratios during dinner time for UF particles were higher than for BC and fine mass, indicating the importance of UF particle indoor sources, likely cooking, and the low indoor-outdoor exchange rates in this location. Kumar et al. (Citation2011) examined improvements in spatial and temporal estimates of ambient PM2.5 and PM10 based on fine-resolution satellite-based aerosol optical depth (AOD). They computed AOD estimates at 2, 5, and 10 km using data from the MODerate Resolution Imaging Spectroradiometer (MODIS) satellite and compared the results to in-situ measurements obtained from NASA's network of sunphotometers (Aerosol RObotic NETwork [AERONET]). MODIS AOD estimates were corrected for meteorological conditions and an empirical regression model was developed to estimate ambient surface PM from the AOD data. For comparison, ambient PM2.5 and PM10 data were obtained from EPA's national Federal Reference Method network. Satellite AOD at 2 km resolution provided better spatial and temporal estimates of PM than the coarse resolution MODIS data. AOD-PM site specific regression slopes varied from 0.52 to 1.72, although on average the slope was close to 1.

Three papers addressed air pollutants and health effects. Faiola et al. (Citation2011) describe an in vitro toxicological study designed to better understand the biological mechanisms of UF particles on adverse health effects. UF particles were collected over two week periods using a high volume size fractionating sample (ChemVol). A dense polypropylene filter, last in the series was used to collect the UF particles. Samples were collected at an urban and rural site in and near Seattle, WA. The authors examined the effect of UF bulk mass, trace metals, labile Fe(II) and easily reducible Fe(III), polycyclic aromatic hydrocarbons (PAH) particles, and surface (1–10 nm) chemistry, the latter specifically C, N, Si, O, and S on the electron transport chain (ETC) in mitochondria isolated from bovine heart tissue. A succinate oxidase activity assay was used to assess ETC function in mitochondria. Strongest correlations between ETC inhibition and measured components were obtained at 5 min with Fe(II)5 min (an aliquot taken after 5 min of reaction time) and anthracene. After 20 min the strongest correlations were observed with sum of PAH species and Fe(II)5 min. ETC inhibition did not correlate with other trace metals or with pooled redox active metals or catalytic metals. These results suggest a mechanism that allows reactive oxygen species to build up, since the O2 normally reduced to H2O in fully functioning mitochondria converts to a superoxide radial (O2 •−), from which other ROS species are formed, such as, OH via the Fenton reaction.

Cahill et al. (2011b; 2011c) investigate the correlation of trace metals in PM and ischemic heart disease (IHD) in the California's Central Valley. In the first of these two papers, very fine and UF aerosol samples were collected along an N-S transect within the Central Valley from Redding to Bakersfield during 17 consecutive days in January 2009. A typical extended stagnation period occurred during this time period in the valley. Sites were located at existing California Air Resources Board (ARB) and district monitoring sites where supplemental data were collected. This study employed an 8-stage drum impactor covering the particle size range from 10 μm to 90 nm and an additional backup filter collecting particles less than 90 nm. Samples were collected every three hours and analyzed for mass and elements from Al to Mo plus Pb. Mass by the drum sampler was compared to the FRM with agreement to better than few percent during the winter, 10% on average over an independent year long evaluation. A second drum impactor was used to collect samples for organic species analysis, although the analysis was averaged over the full 17 day period. Organic species included PAHs, levoglucosan, fatty acids, and n-alkanes. IHD data were obtained from the California Department of Health Services (CA DHS). The strongest correlations of pollutants with IHD were observed between very fine and UF metals, most tied to motor vehicular sources (diesel and gasoline). Results were supported by an independent near roadway study in Sacramento, CA indicating the presence of the same motor vehicular components (non-soil Fe, Ni, Cu, Zn that are associated with brake wear and Zn thiophosphate an additive in lubricating oil) as correlated with IHD in the transect study. Removal of Zn thiophosphate from lubricating oil in motor vehicles and changes in brake drums and pads could reduce these components, and thus, potentially reduce the occurrence of IHD in the valley. Cahill et al. (2011c) compare historical Ni and V levels observed in the California Central Valley and the relationship of lower concentrations of these components in the 2003–2007 time frame versus prior to 1990 when a switch was made from burning crude oil to natural gas to generate steam to enhance petroleum recovery. In 1989–1991, IHD mortality rates were 60% higher in the southern San Joaquin Valley, where most oil production occurred, relative to the rest of the Central Valley. In 2003–2007, a 30% reduction in IHD was observed in the southern part of the valley as compared to those observed in the Sacramento valley, suggesting that the reduction in Ni and V due to the switch from oil to natural gas may have resulted in the reduction of IHD in the southern valley.

The final two papers in this special issue describe the development and/or evaluation of bioaerosol samplers (Xu and Yao Citation2011; Tan et al. Citation2011, respectively).

In the first paper, six bioaerosol samplers are compared to evaluate their collection efficiency and culturable biological activity in both indoor and outdoor environments. Sampling collection mechanisms included filtration, impaction, liquid impingement, and electrostatic. Factors impacting the biological collection efficiency included the sampling mechanism, impaction velocity, relevant cutoff size of the sampler, and degree of particle embedding in the filter or the collection medium. Collected samples were either directly cultured, or washed or extracted from the collection media. All culture samples were incubated for 2 days for bacteria and 3 days for fungi. Biological collection efficiency for bacteria was determined based on the number of colony forming units observed through manual counting. Bioaerosol diversity for bacteria was obtained by denaturing gradient gel electrophoresis and examining the observed number of bands. Identification of fungal colonies was obtained by washing the agar plates, applying a portion to a microscope slide, and manually identifying and counting the fungi. Results indicated that bioaerosol concentrations and diversity varied among the samplers with differences due to different stresses impacting the bioaerosol activity as a result of the different sampler designs and sampling environments. Results also differed among samplers in terms of which reported the highest bioaerosol concentration and which had the greatest diversity. Culturing method also impacted activity and diversity. Tan et al. (Citation2011) describe the development and evaluation of an automated electrostatic sampler (AES) for the collection and transport of biologically active aerosol to a variety of biosensors and the reporting of results in real time. The physical collection efficiency of the sampler was obtained by sampling outdoor and indoor particles of different sizes and monitoring particle counts with an optical particle counter. Different flow rates and voltages applied to the AES were tested to optimize the physical collection efficiency. Indoor and outdoor air also was used to obtain biological collection efficiency as compared to a reference sampler. The biological collection efficiency was evaluated at two flow rates. These tests were conducted using the larger central electrode and the voltage set to 20 kv as optimized in the physical collection efficiency study. Biological collection efficiencies within a factor of 3 and closest to the reference were obtained at the lower flow rate tested. Particle charging at the inlet to the AES, also increased collection efficiencies.

ACKNOWLEDGEMENTS

The 2010 AAAR Air Pollution and Health Conference would not have been possible if not for the generous support by a number of sponsors, including the U.S. EPA, Health Effects Institute, American Chemistry Council, American Petroleum Institute, California Air Resources Board–Research Division, Electric Power Research Institute, NARSTO, National Aeronautics and Space Administration, National Institute for Public Health and the Environment (RIVM), National Oceanic and Atmospheric Administration, South Coast Air Quality Management District, Southern Company, Air & Waste Management Association, International Society of Exposure Sciences, and Springer. The AAAR (the professional society sponsoring the meeting), along with Association Headquarters, AAAR's management company, also were pivotal in making the conference a huge success. I especially thank the conference co-chair, Maria Costantini, conference committee members, and those who attended and participated in the meeting.

Preparation of this preface was supported by the U.S. EPA through its Office of Research and Development. The preface has been subjected to the agency's administrative review and approved for publication.

Paul A. Solomon

U.S. Environmental Protection Agency

Office of Research and Development

Las Vegas, Nevada

E-mail: [email protected]

Paul A. Solomon, a senior environmental scientist with the National Exposure Research Laboratory, Office of Research and Development, at the U.S. EPA in Las Vegas, Nevada, organized and chaired the AAAR Air Pollution and Health International Specialty Conference along with Dr. Maria Costantini of HEI. His research interests include developing and evaluating air quality measurement methods and conducting measurement projects in support of regulatory and research programs in the atmospheric sciences, and in air pollution exposure and health effects programs with an emphasis on particulate matter.

This article not subject to United States Copyright Law.

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