Anthropogenic Particulate Matter Research Articles

Temporal Variation and Sources of Particulate Matter in Kannur: Insights from a Coastal City in South India

In this study, particulate matter (PM) variation has been analyzed to address the dearth of scientific research on air pollution in a coastal city from south India. Mean PM2.5 and PM10 concentrations were 61.6 ± 26.4 and 87.3 ± 35.4 μg/m3. The highest (lowest) seasonal concentration was observed during winter (monsoon). Increase in PM from September to February is attributed to low relative humidity, biomass burning in nearby paddy fields, and continental air mass from the east and north-easterly direction. The mean PM2.5/PM10 ratio was 0.71, with the seasonal ratio ranging between 0.64 (summer) and 0.76 (monsoon), indicating the dominance of anthropogenic PM fraction. PM exhibited typical characteristic of the urban region, i.e., a two-peak diurnal trend during all seasons except monsoon. PM10 (PM2.5) concentrations decreased by ∼7–24.2% (∼11–21%) on the weekends, with the highest reduction in winter seasons. Regarding correlation analysis among PM, CO, and ozone; a negative correlation between PM10 and O3 and a positive correlation between PM and CO was observed. Wind speed and PM10 showed a positive quadratic linear, whereas wind speed and PM2.5 showed a negative linear relationship. The primary sources of particulate matter in Kannur town are motor vehicle emissions, dust from construction work in surrounding zones, and nearby industrial units.

Secondary organic aerosols derived from intermediate-volatility n-alkanes adopt low-viscous phase state

Abstract. Secondary organic aerosol (SOA) derived from n-alkanes, as emitted from vehicles and volatile chemical products, is a major component of anthropogenic particulate matter, yet the chemical composition and phase state are poorly understood and thus poorly constrained in aerosol models. Here we provide a comprehensive analysis of n-alkane SOA by explicit gas-phase chemistry modeling, machine learning, and laboratory experiments to show that n-alkane SOA adopts low-viscous semi-solid or liquid states. Our study underlines the complex interplay of molecular composition and SOA viscosity: n-alkane SOA with a higher carbon number mostly consists of less functionalized first-generation products with lower viscosity, while the SOA with a lower carbon number contains more functionalized multigenerational products with higher viscosity. This study opens up a new avenue for analysis of SOA processes, and the results indicate few kinetic limitations of mass accommodation in SOA formation, supporting the application of equilibrium partitioning for simulating n-alkane SOA formation in large-scale atmospheric models.

Seasonal Variations in Anthropogenic and Natural Particles Induced by Rising CO2 Levels

Using an aerosol–climate coupled model, this paper has investigated the changes in distributions of anthropogenic and natural particles due to 4 × CO2-induced global warming, under the low emission scenario of Representative Concentration Pathway 4.5 (RCP4.5). Special attention is paid to the seasonal variations of aerosol size modes. With rising CO2 levels, surface warming, and changes in atmospheric circulations and hydrologic cycles are found during both summer (JJA) and winter (DJF). For anthropogenic particles, changes in fine anthropogenic particulate matter (PM2.5, particles with diameters smaller than 2.5 μm) decrease over high-latitude regions and increase over the tropics in both DJF and JJA. Global mean column concentrations of PM2.5 decrease by approximately 0.19 mg m−2, and concentrations of coarse anthropogenic particles (CPM, particles with diameters larger than 2.5 μm) increase by 0.005 mg m−2 in JJA. Changes in anthropogenic particles in DJF are similar to those in JJA, but the magnitudes of maximum regional changes are much smaller than those in JJA. The coarse anthropogenic particles (CPM, particles with diameters larger than 2.5 μm) increase over northern Africa and the Arabian Peninsula during JJA, whereas changes in anthropogenic CPM during DJF are minimal. During both JJA and DJF, changes in anthropogenic CPM are about two orders of magnitude smaller than those of anthropogenic PM2.5. Enhanced wet deposition by large-scale precipitation under rising CO2-induced surface warming is the critical factor affecting changes in anthropogenic particles. For natural particles, the distribution of change in the natural PM2.5 burden is similar to that of natural CPM, but much larger than natural CPM during each season. Both natural PM2.5 and CPM burdens increase over northern Africa and the Arabian Peninsula during JJA, but decrease over most of the continental regions during DJF. Changes in surface wind speed, divergence/convergence of surface wind, and precipitation are primary reasons for the variation of natural particles.

Predictability Augmentation by In-silico Study to In-vivo and In-vitro Results of Lung Doses of Airborne Fine and Ultrafine Particles Inhaled by Humans at Industrial Workplaces

This study correlates computational predictions with in vivo and in vitro experimental results of inhaled fine and ultrafine particulate matter (PM) transport, dissemination, and deposition in the human respiratory airways. Epidemiological studies suggest that workplace exposure to anthropogenic pollutant PMs is a risk factor for increased susceptibility to acute broncho-pulmonary illnesses. However, investigations on detailed human inhalation and PM transport processes are restrictive from time, cost, and ethical perspectives. Computational simulation based on the Multiple Path Particle Dosimetry (MPPD) model was employed to quantify the risks associated with workplace exposure of these PMs. Here, the physical, mechanical, and electrical properties of PMs of carbon black (CB) and ultrafine particles (UFPs) from wire-cut electrical discharge machining (WEDM), with mass median aerodynamic diameter (CMAD) in the range of 1 nm to 1000 nm, were used as input parameters of MPPD. Additionally, it mimicked occupational workers’ age, body mass index, and oronasal-combinational nose and mouth breathing exposure time. The deposition results were compared with several vivo and in vitro experimental data reported in the literature, and satisfactory agreements were found. For example, a total lung dose of CB-PMs of 100 nm is the highest (28%), while a 380 nm dose is the lowest (15%). Afterward, deposition increases with particle size, reaching 26% for 1000 nm. In the case of WEDM-UFPs, about 98% of all 1.0 nm inhaled particles remain in the lung. Subsequently, the deposition dose decreases with the particle size and reaches up to 28% for 100 nm particles. Approximately 51% of deposited WEDM-UFPs are of CMAD ≤ 5 nm. The images of lung geometry also observed the maximum deposited mass and mass flux rate in the head, tracheobronchial, and pulmonary airways.

Campfire Smoke and the Anthropocene

Homo sapiens burned wood for warmth and cooking for hundreds of thousands of years. The empiricism that dominates the Anthropocene, however, illuminates the harmful impact of wood smoke on human health. We leveraged the empirical case of campground visitors’ exposure to anthropogenic particulate matter (PM2.5 and PM10) from wood burning at Prince William Forest Park, Virginia, USA to provide a window into the microspatial air quality indexes produced by discretionary campfires. Binary logistic regression illustrates the significant relationship between particulate matter and campfire usage, suggesting multiple potential responses for recreationists, land managers, and scholars. We then transition from “is” to “ought” questions about the ethics of discretionary exposure to particulate matter through wood burning for leisure, an exercise afforded by the epoch. Ultimately, this inquiry yields both practical implications for campfire management and contributes to the more esoteric, ongoing conversations about the connection between fire and our fundamental humanity.

Comprehensive characterization of wintertime submicron aerosol in a Nordic town influenced by residential wood combustion, traffic and industrial sources

Anthropogenic particulate matter with sizes smaller than 1 μm (PM1) is a concerning air pollutant that can affect human health. In this study, we present PM1 measurements performed in a small town in northern Finland that is exposed to contrasting sources (residential wood burning, traffic, industrial activities). The study was conducted in winter 2021, with a mobile laboratory equipped with sophisticated on-line aerosol instrumentation. The results showed a significant increase in particulate mass and number concentrations from biomass burning in residential areas and town centre due to the high share of residences using biomass burning. Organics and equivalent black carbon (eBC) clearly dominated the PM1 composition during the highest pollution levels, followed by inorganics (sulfate, nitrate and ammonium). PAHs and a few elements (e.g. K, Cl, Zn) were as well higher during evening. A source apportionment confirmed the association between high PM1 values and biomass burning, even though the traffic contribution was also important. PM1 measurements at an industrial area showed an increase in sulfate, organics, eBC, and a few elements (e.g. Cl, Na, Fe), and characteristic size distributions. Simultaneous measurements of lung deposited surface area (LDSA) of particles showed the source-specificity of biomass burning, traffic and industrial emissions on LSDA size distributions. Overall, the results enlighten the impact of relevant pollution sources on Nordic towns air quality during the coldest months and show the importance to also consider the chemical composition, particle numbers, and LDSA in future air quality metrics.

Coarse particulate matter air quality in East Asia: implications for fine particulate nitrate

Abstract. Air quality network data in China and South Korea show very high year-round mass concentrations of coarse particulate matter (PM), as inferred by the difference between PM10 and PM2.5. Coarse PM concentrations in 2015 averaged 52 µg m−3 in the North China Plain (NCP) and 23 µg m−3 in the Seoul Metropolitan Area (SMA), contributing nearly half of PM10. Strong daily correlations between coarse PM and carbon monoxide imply a dominant source from anthropogenic fugitive dust. Coarse PM concentrations in the NCP and the SMA decreased by 21 % from 2015 to 2019 and further dropped abruptly in 2020 due to COVID-19 reductions in construction and vehicle traffic. Anthropogenic coarse PM is generally not included in air quality models but scavenges nitric acid to suppress the formation of fine particulate nitrate, a major contributor to PM2.5 pollution. GEOS-Chem model simulation of surface and aircraft observations from the Korea–United States Air Quality (KORUS-AQ) campaign over the SMA in May–June 2016 shows that consideration of anthropogenic coarse PM largely resolves the previous model overestimate of fine particulate nitrate. The effect is smaller in the NCP which has a larger excess of ammonia. Model sensitivity simulations for 2015–2019 show that decreasing anthropogenic coarse PM directly increases PM2.5 nitrate in summer, offsetting 80 % the effect of nitrogen oxide and ammonia emission controls, while in winter the presence of coarse PM increases the sensitivity of PM2.5 nitrate to ammonia and sulfur dioxide emissions. Decreasing coarse PM helps to explain the lack of decrease in wintertime PM2.5 nitrate observed in the NCP and the SMA over the 2015–2021 period despite decreases in nitrogen oxide and ammonia emissions. Continuing decrease of fugitive dust pollution means that more stringent nitrogen oxide and ammonia emission controls will be required to successfully decrease PM2.5 nitrate.

Physicochemical Characterization of Aerosols in the Coastal Zone: Evidence of Persistent Carbon Soot in the Marine Atmospheric Boundary Layer (MABL) Background

Aerosol particles in coastal areas result from a complex mixing between sea-spray aerosols locally generated at the sea surface by breaking waves and a continental component issued from natural and/or anthropogenic sources. The aim of this paper is to study how the aerosols mix in the coastal marine atmosphere to evaluate the impact of the background pollution on the atmospheric aerosols. To this end, we have carried out a qualitative analysis of particulate matter sampled at two French coastal areas using a non-destructive methodology combining scanning electron microscopy (SEM)/X-ray fluorescence, transmission electron microscopy (TEM), X-ray diffraction, and Raman spectroscopy. Our analysis shows a dominant contribution of anthropogenic aerosols through strong levels of submicronic carbon soot and sulfate particles, even observed when the aerosol is sampled during pure maritime-air mass episodes. Our results also evidence the non-mixing between sea-spray, mainly composed of coarse aerosol particles, and this anthropogenic particulate matter of smaller sizes.

Size-Based Effects of Anthropogenic Ultrafine Particles on Lysosomal TRPML1 Channel and Autophagy in Motoneuron-like Cells.

An emerging body of evidence indicates an association between anthropogenic particulate matter (PM) and neurodegeneration. Although the historical focus of PM toxicity has been on the cardiopulmonary system, ultrafine PM particles can also exert detrimental effects in the brain. However, only a few studies are available on the harmful interaction between PM and CNS and on the putative pathomechanisms. Ultrafine PM particles with a diameter < 0.1 μm (PM0.1) and nanoparticles < 20 nm (NP20) were sampled in a lab-scale combustion system. Their effect on cell tracking in the space was studied by time-lapse and high-content microscopy in NSC-34 motor neurons while pHrodo™ Green conjugates were used to detect PM endocytosis. Western blotting analysis was used to quantify protein expression of lysosomal channels (i.e., TRPML1 and TPC2) and autophagy markers. Current-clamp electrophysiology and Fura2-video imaging techniques were used to measure membrane potential, intracellular Ca2+ homeostasis and TRPML1 activity in NSC-34 cells exposed to PM0.1 and NP20. NP20, but not PM0.1, reduced NSC-34 motor neuron movement in the space. Furthermore, NP20 was able to shift membrane potential of motor neurons toward more depolarizing values. PM0.1 and NP20 were able to enter into the cells by endocytosis and exerted mitochondrial toxicity with the consequent stimulation of ROS production. This latter event was sufficient to determine the hyperactivation of the lysosomal channel TRPML1. Consequently, both LC3-II and p62 protein expression increased after 48 h of exposure together with AMPK activation, suggesting an engulfment of autophagy. The antioxidant molecule Trolox restored TRPML1 function and autophagy. Restoring TRPML1 function by an antioxidant agent may be considered a protective mechanism able to reestablish autophagy flux in motor neurons exposed to nanoparticles.

Reactive Uptake of Gas-Phase NO2 by Urban Road Dust in the Dark.

Road dust constitutes a prominent source of anthropogenic particulate matter, making its heterogeneous interactions with common atmospheric gas-phase compounds important. Here, we show that three distinct samples of urban road dust-including dust samples collected from city streets in summer and winter, and an urban park in summer-react with NO2 in the dark, forming NO and surface nitrite. The loss of NO2 ranged from ∼2 to 13% of its gas-phase concentration and scaled with its concentration as well as with the mass of the road dust sample. The uptake of NO2 by the winter dust was ∼4 times greater than that seen from summer street dust, which was in turn greater than that by the park dust. The conversion ratio of NO2 → NO ranged from 0.06 to 0.8 NO produced per NO2 lost and was greatest for the summer park dust. Exposure of the summer road dust to NO2 roughly doubles the concentration of inorganic nitrite anion in the dust but does not produce nitrate. The formation of NO and photolabile nitrite products means that heterogeneous NO x reactions occurring on the surface of road dust in the dark could have wide implications for the oxidative potential of urban areas.

Characteristics of Atmospheric Compounds based on Regional Multicorrelation Analysis in Honam Area

Particulate Matter (PM) in the atmosphere has serious impacts on human health and the global environmental systems. To reduce anthropogenic PM emissions is of importance to protect public health. In this study, the variation of concentrations in PM<sub>2.5</sub>, NO<sub>2</sub>, and O<sub>3</sub> of Honam region over the past 6 years (2016-2021) was investigated. A statistical approach (i.e., hierarchical cluster analysis) was performed to present their spatial relationships. As a result, the high concentration of PM<sub>2.5</sub> in Iksan-si was found in sources of primary pollutants emitted from industrial complexes and ammonia from large-scale livestock complexes. The high concentration periods of PM<sub>2.5</sub> with lower concentrations of NO<sub>2</sub> and O<sub>3</sub> can be seasonal and secondary PM product contributions. In addition, the concentration of O<sub>3</sub> in Buan-gun and Wanju-gun with lower PM levels can be the effect of emission of volatile organic compounds (VOC<sub>S</sub>) from sources. It is necessary to strengthen management for reducing emissions by sources and to establish a policy to control precursors of the atmospheric contaminants.

Seasonal variation of atmospheric Pb sources in Singapore - Elemental and lead isotopic compositions of PM10 as source tracer

Southeast Asia has become a hotspot of anthropogenic particulate matter (PM) emissions due to increased coal combustion, high-temperature industrial operations, vehicular traffic, and agricultural biomass burning. Lead (Pb), a criteria pollutant, bound to such PM can be hazardous when inhaled, even at extremely low concentrations. Precise and accurate source apportionment of atmospheric Pb is thus, critical in order to minimize its exposure. This study investigates the sources of atmospheric Pb in Singapore aerosol samples (PM10) using Pb isotopes and elemental composition as tracers of contamination sources. PM10 aerosol sampling was conducted over a period of 1 year from June 2017 to May 2018 to capture the seasonal variations in sources of atmospheric Pb. Elemental concentrations reveal particularly high enrichment factors for Pb, Cu, V, Ni and Zn, especially when under the influence of southwest (SW) and inter monsoon (IM) winds. Pb isotopic ratios across the three seasons (206/207Pb = 1.147˗1.150 and 208/207Pb = 2.420˗2.428) are not significantly different. The Pb isotopic signatures and V/Ni ratios for all three seasons overlap with those of gasoline, diesel and ship emissions. Moreover, V/Pb values of more than unity for SW and IM winds suggest influence of transboundary coal combustion emissions particularly from Indonesia. Consequently, using Pb isotopic fingerprints and elemental ratios, we find that the primary sources of atmospheric Pb are vehicular & ship emissions, heavy oil combustion, transboundary coal combustion emissions, waste incineration and recirculation of historic leaded gasoline.

Size-based effects of anthropogenic ultrafine particles on activation of human lung macrophages.

The anthropogenic particulate matter (PM), suspended air dust that can be inhaled by humans and deposited in the lungs, is one of the main pollutants in the industrialized cities atmosphere. Recent studies have shown that PM has adverse effects on respiratory diseases. These effects are mainly due to the ultrafine particles (PM0.1, PM<100nm), which, thanks to their PM size, are efficiently deposited in nasal, tracheobronchial, and alveolar regions. Pulmonary macrophages are a heterogeneous cell population distributed in different lung compartments, whose role in inflammatory response to injury is of particular relevance. In this study, we investigated the effect of PM0.1 on Human Lung Macrophages (HLMs) activation evaluated as proinflammatory cytokines and chemokine release, Reactive Oxygen Species (ROS) production and intracellular Ca2+concentration ([Ca2+]i). Furthermore, PM0.1, after removal of organic fraction, was fractionated in nanoparticles both smaller (NP20) and bigger (NP100) than 20nm by a properlydeveloped analytical protocol, allowed isolating their individual contribution. Interestingly, while PM0.1 and NP20 induced stimulatory effects on HLM cytokines release, NP100 had not effect. In particular, PM0.1 induced IL-6, IL-1β, TNF-α, but not CXCL8, release from HLMs. Moreover, PM0.1, NP20 and NP100 did not induce β-glucuronidase release, a preformed mediator contained in HLMs. The long time necessary for cytokines release (18h) suggested that PM0.1 and NP20 could induce ex-novo production of the tested mediators. Accordingly, after 6h of incubation, PM0.1 and NP20 induced mRNA expression of IL-6, TNF-α and IL-1β. Moreover, NP20 induced ROS production and [Ca2+]i increase in a time-dependent manner, without producing cytotoxicity. Collectively, the present data highlight the main proinflammatory role of NP20 among PM fractions. This is particularly of concern because this fraction is not currently covered by legal limits as it is not easily measured at the exhausts by the available technical methodologies, suggesting that it is mandatory to search for new monitoring techniques and strategies for limiting NP20 formation.

Source Sector Mitigation of Solar Energy Generation Losses Attributable to Particulate Matter Pollution

Particulate matter (PM) in the atmosphere and deposited on solar photovoltaic (PV) panels reduce PV energy generation. Reducing anthropogenic PM sources will therefore increase carbon-free energy generation and as a cobenefit will improve surface air quality. However, we lack a global understanding of the sectors that would be the most effective at achieving the necessary reductions in PM sources. Here we combine well-evaluated models of solar PV performance and atmospheric composition to show that deep cuts in air pollutant emissions from the residential, on-road, and energy sectors are the most effective approaches to mitigate PM-induced PV energy losses over East and South Asia, and the Tibetan Plateau, Central Asia, and the Arabian Peninsula, and Western Siberia, respectively. Using 2019 PV capacities as a baseline, we find that a 50% reduction in residential emissions would lead to an additional 10.3 TWh yr–1 (US$878 million yr–1) and 2.5 TWh yr–1 (US$196 million yr–1) produced in China and India, respectively.

Sr-Nd-Hf isotopic analysis of reference materials and natural and anthropogenic particulate matter sources: Implications for accurately tracing North African dust in complex urban atmospheres.

We present novel chemical separation protocols for isotopic analysis of low mass aliquots (0.3mg and 25mg) of several reference materials and real-world samples of relevance to urban airborne particulate matter (PM) investigations. A high-yielding gravity flow column chromatography scheme was developed for facile and quantitative separation of Sr, Nd, and Hf prior to multi collector - inductively coupled plasma - mass spectrometry (MC-ICP-MS). Because we are interested in isolating and accurately quantitating individual anthropogenic and natural aerosol sources in complex industrial/metropolitan atmospheric environments, laboratory protocols were optimized using National Institute of Standards and Technology Standard Reference Material (SRM) 1648a (urban atmospheric PM), SRM 1633b (coal fly ash), and European Commission standards BCR-723 (vehicular road dust), and BCR-2 (basalt rock standard). Sr, Nd, and Hf procedural blanks from column chromatography were low (averaging only 37pg, 17pg, 11pg, respectively) and recoveries were high (averaging 95%, 82%, and 92%, respectively). A volume-adjustment protocol was established using isotope reference solutions SRM 987 (SrCO3), JNdi (Nd2O3), and in-house Hf standards to dilute the dried samples prior to MC-ICP-MS based on projected uncertainties for low sample masses. 87Sr/86Sr, 143Nd/144Nd, and 176Hf/177Hf isotopic ratios in SRM 1648a, BCR-723, and SRM 1633b are reported for the first time that can serve as provisional reference values. The novel method was used to characterize isotopic ratios and elemental abundances in two anthropogenic urban aerosol sources, namely motor vehicles and petroleum refining using airborne fine PM collected in a vehicular tunnel and fluidized-bed catalytic cracking catalysts, respectively. Two other important mineral-rich urban PM sources, namely soil (i.e., resuspended crustal material) and concrete/cement dust (i.e., construction activity) were also characterized. These are the first isotopic measurements in these environmental compartments and were compared with literature data for long-range transported North African dust, which is a prominent summertime PM source in urban regions in southeastern United States. We demonstrate the capability of coupled Sr-Nd-Hf isotopes to uniquely trace different mineral dust sources with overlapping elemental composition (Sahara-Sahel region, local soil, and concrete/cement) and accurately isolate various urban PM sources demonstrating the superiority of isotopic markers over elemental tracers.

Wildfire atmospheric chemistry: climate and air quality impacts

Wildfire atmospheric chemistry: climate and air quality impacts

Spatial characteristics of the PM2.5/PM10 ratio and its indicative significance regarding air pollution in Hebei Province, China.

Particulate matter (PM) is the primary air pollutant in northern China. The PM2.5/PM10 ratio has been used increasingly as an indicator to reflect anthropogenic PM pollution, but its advantages compared with individual PM2.5 or PM10 concentrations have not been proven sufficiently by experimental data. By dividing Hebei Province (China) into seven natural ecological regions, this study investigated the spatial characteristics of the PM2.5/PM10 ratio and its relationships with PM2.5, PM10, economic density, and wind speed. Results showed that the PM2.5/PM10 ratio decreased from east to west and from south to north, with an annual average value in 2019 of 0.439-0.559. The characteristics of the spatial variation of the PM2.5/PM10 ratio were different to those of either PM2.5 or PM10 concentration, indicating that PM pollution reflected by the PM2.5/PM10 ratio is not entirely consistent with that by PM2.5 and PM10 concentrations. In comparison with PM2.5 or PM10 concentration, the PM2.5/PM10 ratio had higher (lower) correlation with economic density (wind speed), indicating that the PM2.5/PM10 ratio is a better indicator used to reflect the intensity of anthropogenic emissions of PM pollutants. According to the characteristics of the spatial variations of the PM2.5/PM10 ratio and the PM2.5 and PM10 concentrations, the seven ecological regions of Hebei Province were categorized into four different types of atmospheric PM pollution: "three low regions," "three high regions," "one high and two low regions," and "one low and two high regions." This reflects the comprehensive effect of the intensity of anthropogenic PM emissions and the atmospheric diffusion conditions.

Statistical Thermodynamic Description of Heteroaggregation between Anthropogenic Particulate Matter and Natural Particles in Aquatic Environments

Aggregation is a key process in understanding the fate and transport of anthropogenic particulate matter, namely, nanoparticles and microplastics, in aquatic environments. Recent research has subdi...

Oxidative stress-induced inflammation in susceptible airways by anthropogenic aerosol.

Ambient air pollution is one of the leading five health risks worldwide. One of the most harmful air pollutants is particulate matter (PM), which has different physical characteristics (particle size and number, surface area and morphology) and a highly complex and variable chemical composition. Our goal was first to comparatively assess the effects of exposure to PM regarding cytotoxicity, release of pro-inflammatory mediators and gene expression in human bronchial epithelia (HBE) reflecting normal and compromised health status. Second, we aimed at evaluating the impact of various PM components from anthropogenic and biogenic sources on the cellular responses. Air-liquid interface (ALI) cultures of fully differentiated HBE derived from normal and cystic fibrosis (CF) donor lungs were exposed at the apical cell surface to water-soluble PM filter extracts for 4 h. The particle dose deposited on cells was 0.9–2.5 and 8.8–25.4 μg per cm2 of cell culture area for low and high PM doses, respectively. Both normal and CF HBE show a clear dose-response relationship with increasing cytotoxicity at higher PM concentrations. The concurrently enhanced release of pro-inflammatory mediators at higher PM exposure levels links cytotoxicity to inflammatory processes. Further, the PM exposure deregulates genes involved in oxidative stress and inflammatory pathways leading to an imbalance of the antioxidant system. Moreover, we identify compromised defense against PM in CF epithelia promoting exacerbation and aggravation of disease. We also demonstrate that the adverse health outcome induced by PM exposure in normal and particularly in susceptible bronchial epithelia is magnified by anthropogenic PM components. Thus, including health-relevant PM components in regulatory guidelines will result in substantial human health benefits and improve protection of the vulnerable population.

Nanostructural Disorder and Reactivity Comparison of Flame Soot and Engine Soot Using Diesel and Jatropha Biodiesel/Diesel Blend as Fuels

Soot is a major anthropogenic air pollutant that affects human health and contributes to global warming. To understand its formation pathways and reduce emission, several flame and engine studies exist in the literature, though the fundamental differences in the characteristics of engine and flame soots are not well understood. This study presents a detailed comparative investigation of soot nanostructural properties and their relationship with the oxidative reactivity of soots from an engine and a diffusion flame using diesel and 20% Jatropha biodiesel/diesel blend fuels. X-ray diffraction, Raman spectroscopy, high-resolution transmission electron microscopy, electron energy loss spectroscopy, and thermogravimetric analyses confirm that engine soot has greater primary particle diameter, higher concentration of loosely held aliphatics, greater degree of graphitized nanocrystallites with lower interplanar separation, longer fringe lengths, lower tortuosity, and greater resistance for oxidation than the flame soot, though the differences in several properties were minor. The effects of biodiesel addition to diesel on soot properties and sooting tendency were predicted very well with both flame and engine setup. Moreover, the enhanced soot oxidation in the combustor catalyzed by fuel-bound oxygen in biodiesel further reduces the nanostructural and reactivity differences between engine and flame soots. Though engine soot properties have more relevance to anthropogenic particulate matter, flame setups appear to be suitable for screening and studying the effect of fuel additives on the sooting propensity and physicochemical properties of soot prior to their testing and utilization in engines.