Fraction Of Fine Particulate Matter Research Articles

Studies on the reduction of dispersed emissions from a low-power household boiler in a plasma ionic wind zone

Gas ionizator is a device for electrostatic precipitation and is widely used to separate fine particulate matter (FPM) from small- and large-scale industrial exhaust gases. Two variations of electrodes design, rod and rectangle-toothed saw were used. The mass and number concentrations of six FPM fractions were detected. Stronger vortices occur at higher EAD/Re2 ratios compared to the secondary electroaerodynamic (EAD) gas velocities. A deposition efficiency higher than 94.9 % was achieved at a gas velocity of 0.2 m/s. The FPM capture efficiency at voltage up to 20 kV is higher more than 7 % than at a voltage of 15 kV.

Gravimetric, morphological, and chemical characterization of fine and ultrafine particulate matter inside fire stations

Poor air quality inside buildings has direct implications for human health. The activity of firefighters causes cancer and promotes the development/aggravation of cardio-respiratory diseases. The indoor air quality inside fire stations remains poorly characterized. This work assesses firefighters’ daily exposure to fine (PM2.5, PM156nm) and ultrafine (PM50.4nm, PM30.8nm) particulate matter (PM) inside three microenvironments of fire stations, and, for the first time, characterizes the morphology and elemental content of collected PM. Fine PM fractions were predominant in all microenvironments. Fine and ultrafine PM concentrations were increased in the personal protective equipment (PPE) storage room than in the common area and garage [11.84–103.5 μg/m3versus 18.67–51.89 μg/m3 and 22.57–70.69 μg/m3; p > 0.05 and 4.78–46.02 μg/m3versus 3.03–40.99 μg/m3 and 5.55–23.30 μg/m3; p > 0.05]; values were below the guideline proposed for occupational exposure to respirable dust (5.0 mg/m3). The morphological analysis revealed the presence of organic matter, microorganisms, crystals, minerals, metals, and other unidentified substances in fine/ultrafine PM. Exposure to total PM-bound metals was increased in the garage comparatively to the common area and the PPE storage room (2765.0–46586.0 pg/m3versus 2414.2–4568.6 pg/m3; p > 0.5). Cu, Zn, and Cr were the predominant PM-bound metals while Sb, Cd, and Tl were the less abundant. Exposure to PM-bound possible/probable carcinogenic metals (Ni, Cd, Sb, and Pb) accounted for 7.81–10.72% and 0.342–13.07% of fine and ultrafine PM, respectively. The data generated can support regulatory agencies in proposing air quality guidelines that promote occupational safety and health.

On the sources of ambient SOA in PM2.5: An integrated analysis over Jinan city of China

Secondary organic aerosol (SOA) accounts for a significant fraction of fine particulate matter (PM2.5) and is a crucial component that affects climate and public health. However, the formation of SOA in urban areas remains unclear and sources contributed to SOA are poorly characterized. In this study, we combined ambient measurements and the Weather Research and Forecasting (WRF)-Community Multi-scale Air Quality (CMAQ) modeling system to investigate the evolution of SOA during winter over Jinan city in China. Relative contributions of different anthropogenic sources to ambient SOA were subsequently probed by the Integrated Source Apportionment Method (ISAM) to explore the impact of anthropogenic emissions. The mean concentration of SOA was 11.2 μg m−3, accounting for 29.4% in PM2.5, and SOA concentrations on clean days (4.9 μg m−3) increased by 4.8 times on polluted days (23.3 μg m−3), and strong correlation between the elevated PM2.5 episodes and increased SOA concentrations was found (R2 > 0.5). In addition, SOA concentrations and the proportion of SOA in PM2.5 were higher during the daytime (24.9 μg m−3, 32.4%) compared to nighttime (21.9 μg m−3, 25.1%) on polluted days, which is primarily attributed to the intense atmospheric photochemical reactions and anthropogenic activities. Mobile sources act as the dominant contributor to SOA (57.6%) and road diesel emissions (30.9%) made the largest contribution to SOA, followed by non-road mobile sources (17.4%) among subsectors in mobile sources. This study sheds new insights into ambient SOA formation and SOA source apportionment for typical megacities in China, guiding the design of source-oriented regulation efforts on SOA mitigation.

Particulate Matter Load Estimation and Distribution Characteristics of Diesel Particulate Filter

This paper focuses on the offline electric heating regeneration technology of DPF (Diesel Particulate Filter). Based on the actual operating conditions of the airport passenger elevator, the pressure drop changes before and after the offline regeneration of DPF, the passive regeneration process during the vehicle operation, and the capture efficiency of PM and PN after the offline regeneration of DPF are studied. The DPF pressure drop increases with the operation time because of the extremely low efficiency of passive regeneration before offline regeneration, and the initial pressure drop after regeneration is slightly higher than that of the fresh carrier due to the existence of ash. When the exhaust temperature reaches 420°C, the DPF passive regeneration rate is higher than the capture rate, and the DPF pressure drop drops rapidly when the passenger elevator continues to run. The mass fraction of fine particulate matter is more than 0.02μm in the cold start stage, while the mass fraction of fine particulate matter is more than 0.02μm in the hot start stage.

Characterization of products formed from the oxidation of toluene and m-xylene with varying NOx and OH exposure

Aromatic volatile organic compounds (VOCs) are an important precursor of secondary organic aerosol (SOA) in the urban environment. SOA formed from the oxidation of anthropogenic VOCs can be substantially more abundant than biogenic SOA and has been shown to account for a significant fraction of fine particulate matter in urban areas. A potential aerosol mass (PAM) chamber was used to investigate the oxidised products from the photo-oxidation of m-xylene and toluene. The experiments were carried out with OH radical as oxidant in both high- and low-NOx conditions and the resultant aerosol samples were collected using quartz filters and analysed by GC × GC-TOFMS. Results show the oxidation products derived from both precursors included ring-retaining and -opening compounds (unsaturated aldehydes, unsaturated ketones and organic acids) with a high number of ring-opening compounds observed from toluene oxidation. Glyoxal and methyl glyoxal were the major ring-cleavage products from both oxidation systems, indicating that a bicyclic route plays an important role in their formation. SOA yields were higher for both precursors under high-NOx (toluene: 0.111; m-xylene: 0.124) than at low-NOx (toluene: 0.089; m-xylene: 0.052), likely linked to higher OH concentrations during low-NOx experiments which may lead to higher degree of fragmentation. DHOPA (2,3-dihydroxy-4-oxo-pentanoic acid), a known tracer of toluene oxidation, was observed in both oxidation systems. The mass fraction of DHOPA in SOA from toluene oxidation was about double the value reported previously, but it should not be regarded as a tracer solely for oxidation of toluene as m-xylene oxidation gave a similar relative yield.

69 Activation of the Aryl Hydrocarbon Receptor - a Major mode of Combustion Particle Toxicity?

Abstract Combustion-derived particles constitute an important part of the fine fraction of particulate matter with aerodynamic diameter less than 2.5 microns (PM2.5) and are considered central for the adverse effects of air pollution. Understanding the mechanisms of combustion particle toxicity may shed light on the components and characteristics of outdoor air PM driving adverse health effects. This may also enable more targeted and efficient policies to improve air quality and promote health and wellbeing. The aryl hydrocarbon receptor (AhR) is a ligand dependent transcription factor, originally discovered for its ability to bind polycyclic aromatic hydrocarbons (PAHs) and dioxin-like compounds and regulate PAH metabolism. It is now clear that AhR regulates a variety of biological and toxicological responses, overlapping to a considerable degree with the effects of combustion PM and ambient PM2.5. Studies from our lab and others also suggest that AhR activation is among the most sensitive responses to combustion PM exposure, induced at orders of magnitude lower concentrations than many other endpoints. This talk will discuss the potential role of the AhR and PAHs in combustion PM toxicity based on previous and ongoing work, with a main focus on intracellular signalling and regulation of inflammatory reactions in lung epithelial cells and vascular endothelial cells.

Linking Cell Health and Reactive Oxygen Species from Secondary Organic Aerosols Exposure.

Oxidative stress is a possible mechanism by which ambient fine particulate matter (PM) exerts adverse biological effects. While multiple biological effects and reactive oxygen species (ROS) production have been observed upon PM exposure, whether the biological effects are ROS-mediated remains unclear. Secondary organic aerosols (SOA) constitute a major fraction of fine PM and can contribute substantially to its toxicity. In this work, we measured three types of cell responses (mitochondrial membrane potential (MMP), caspase 3/7 activity, and ROS) and investigated their associations upon exposure to SOA formed from anthropogenic (naphthalene) and biogenic (α-pinene) precursors. MMP and caspase 3/7 activity (an early indicator of apoptosis) are key indicators of cell health, and changes of them could occur downstream of ROS-mediated pathways. We observed a significant increase in caspase 3/7 activity after SOA exposure, suggesting that apoptosis is an important pathway of cell death induced by SOA. We further found strong associations between a decrease in MMP and increase in caspase 3/7 activity with an increase in cellular ROS level. These results suggest that cell health is largely dependent on the cellular ROS level, highlighting oxidative stress as a key mechanism for biological effects from SOA exposure. Linear regression analyses reveal greater changes of the three cellular responses with increasing carbon oxidation state (OSc) of SOA, suggesting that SOA are more toxic when they are more oxidized. Overall, our work provides critical insights into the associations between cell health and ROS level upon SOA exposure and proposes that OSc could be a suitable proxy to assess the overall SOA toxicity.

Role of Secondary Organic Matter on Soot Particle Toxicity in Reconstituted Human Bronchial Epithelia Exposed at the Air-Liquid Interface.

Secondary organic matter (SOM) formed from gaseous precursors constitutes a major mass fraction of fine particulate matter. However, there is only limited evidence on its toxicological impact. In this study, air-liquid interface cultures of human bronchial epithelia were exposed to different series of fresh and aged soot particles generated by a miniCAST burner combined with a micro smog chamber (MSC). Soot cores with geometric mean mobility diameters of 30 and 90 nm were coated with increasing amounts of SOM, generated from the photo-oxidation of mesitylene and ozonolysis of α-pinene. At 24 h after exposure, the release of lactate dehydrogenase (LDH), indicating cell membrane damage, was measured and proteome analysis, i.e. the release of 102 cytokines and chemokines to assess the inflammatory response, was performed. The data indicate that the presence of the SOM coating and its bioavailability play an important role in cytotoxicity. In particular, LDH release increased with increasing SOM mass/total particle mass ratio, but only when SOM had condensed on the outer surface of the soot cores. Proteome analysis provided further evidence for substantial interference of coated particles with essential properties of the respiratory epithelium as a barrier as well as affecting cell remodeling and inflammatory activity.

Superoxide Release by Macrophages through NADPH Oxidase Activation Dominating Chemistry by Isoprene Secondary Organic Aerosols and Quinones to Cause Oxidative Damage on Membranes.

Oxidative stress mediated by reactive oxygen species (ROS) is a key process for adverse aerosol health effects. Secondary organic aerosols (SOA) account for a major fraction of fine particulate matter, and their inhalation and deposition into the respiratory tract causes the formation of ROS by chemical and cellular processes, but their relative contributions are hardly quantified and their link to oxidative stress remains uncertain. Here, we quantified cellular and chemical superoxide generation by 9,10-phenanthrenequinone (PQN) and isoprene SOA using a chemiluminescence assay combined with electron paramagnetic resonance spectroscopy as well as kinetic modeling. We also applied cellular imaging techniques to study the cellular mechanism of superoxide release and oxidative damage on cell membranes. We show that PQN and isoprene SOA activate NADPH oxidase in macrophages to release massive amounts of superoxide, overwhelming the superoxide formation by aqueous chemical reactions in the epithelial lining fluid. The activation dose for PQN is 2 orders of magnitude lower than that of isoprene SOA, suggesting that quinones are more toxic. While higher exposures trigger cellular antioxidant response elements, the released ROS induce oxidative damage to the cell membrane through lipid peroxidation. Such mechanistic and quantitative understandings provide a basis for further elucidation of adverse health effects and oxidative stress by fine particulate matter.

Sources and processes of organic aerosol in non-refractory PM1 and PM2.5 during foggy and haze episodes in an urban environment of the Yangtze River Delta, China

Organic aerosol (OA) generally accounts for a large fraction of fine particulate matter (PM2.5) in the urban atmosphere. Despite significant advances in the understanding their emission sources, transformation processes and optical properties in the submicron aerosol fraction (PM1), larger size fractions - e.g., PM2.5 - still deserve complementary investigations. In this study, we conducted a comprehensive analysis on sources, formation process and optical properties of OA in PM1 and PM2.5 under haze and foggy environments in the Yangtze River Delta (eastern China), using two aerosol chemical speciation monitors, as well as a photoacoustic extinctiometer at 870 nm. Positive matrix factorization analysis - using multilinear engine (ME2) algorithm - was conducted on PM1 and PM2.5 organic mass spectra. Four OA factors were identified, including three primary OA (POA) factors, i.e., hydrocarbon-like OA (HOA), cooking OA (COA), and biomass burning OA (BBOA), and a secondary OA (SOA) factor, i.e., oxidized oxygenated OA (OOA). An enhanced PM1-2.5 COA concentration was clearly observed during cooking peak hours, suggesting important contribution of fresh cooking emissions on large-sized particles (i.e., PM1-2.5). The oxidation state and concentration of PM2.5 HOA were higher than that in PM1, suggesting that large-sized HOA particles might be linked to oxidized POA. High contribution (44%) of large-sized OOA to non-refractory PM2.5 mass was observed during haze episodes. During foggy episodes, PM1 and PM2.5 OOA concentrations increased as a positive relationship over time, along with an exponential increase in the PM2.5-OOA to PM1-OOA ratio. Meanwhile, OOA loadings increased with the aerosol liquid water content (ALWC) during foggy episodes. Random forest cross-validation analysis also supported the important influence of ALWC on OOA variations, supporting substantial impact of aqueous process on SOA formation during haze and/or foggy episodes. Obtained results also indicated high OOA contributions (21%–36%) and low POA contributions (6%–14%) to the PM2.5 scattering coefficient during haze and foggy episodes, respectively. Finally, we could illustrate that atmospheric vertical diffusion and horizontal transport have important but different effects on the concentrations of different primary and secondary OA factors in different particle size fractions.

Airborne bacterial community associated with fine particulate matter (PM2.5) under different air quality indices in Temuco city, southern Chile.

Temuco (Chile) is one of the most polluted cities in Chile and Latin America. Although the fine fraction of particulate matter (PM2.5) has been extensively studied and monitored due to its negative impact on public health, its microbiological components remain unknown. We explored, the airborne bacterial community in PM2.5 under good, moderate, alert, pre-emergency and emergency indices of air quality (AQIs) established by the Chilean government. Bacterial community relationship with environmental factors (PM2.5, PM10, carbon monoxide, among others), was also evaluated. Significant differences in PM2.5 bacterial community composition associated with AQIs were revealed, using 16S rRNA target sequences of denaturing gradient gel electrophoresis (DGGE) bands. Bacterial communities in PM2.5 were mainly clustered (80%) into emergency and pre-emergency samples. The dominant phylum was Proteobacteria and most abundant genus was Novosphingobium, traditionally related to opportunistic respiratory diseases. The main factors associated with community structure were PM2.5, PM10 and carbon monoxide concentrations. This study exposed that bacterial community composition in Temuco varies according to AQIs, with the occurrence of potential opportunistic bacteria on heavily polluted days.Supplementary InformationThe online version contains supplementary material available at 10.1007/s00203-021-02740-6.

Occurrence and in vitro toxicity of organic compounds in urban background PM2.5

This study describes the chemical composition and in vitro toxicity of the organic fraction of fine particulate matter (PM2.5) at an urban background site, which receives emissions either from Frankfurt international airport or the city centre, respectively. We analysed the chemical composition of filter extracts (PM2.5) using ultrahigh-performance liquid chromatography coupled to a high-resolution mass spectrometer, followed by a non-target analysis. In parallel, we applied the bulk of the filter extracts to a Microtox and acetylcholinesterase-inhibition assay for in vitro toxicity testing. We find that both the chemical composition and toxicity depend on the prevailing wind directions, and the airport operating condition, respectively. The occurrence of the airport marker compounds tricresyl phosphate and pentaerythritol esters depends on the time of the day, reflecting the night flight ban as well as an airport strike event during November 2019. We compared the organic aerosol composition and toxicity from the airport wind-sector against the city centre wind-sector. We find that urban background aerosol shows a higher baseline toxicity and acetylcholinesterase inhibition compared to rural PM2.5 that is advected over the airport. Our results indicate that the concentration and individual composition of PM2.5 influence the toxicity. Suspected drivers of the acetylcholinesterase inhibition are i.e. organophosphorus esters like triphenyl phosphate and cresyldiphenyl phosphate, and the non-ionic surfactant 4-tert-octylphenol ethoxylate. However, further research is necessary to unambiguously identify harmful organic air pollutants and their sources and quantify concentration levels at which adverse effects in humans and the environment can occur.

Characteristics of atmospheric air pollution by fine particles based on regional monitoring data

Introduction. Air pollution with particulate matter (PM) is a serious global problem. In the Russian Federation, regular field measurements of PMs in the ambient air are carried out only in a few cities, and the data, as a rule, are not systematized. Aim of the study: long-term analysis of the data set on concentrations of fine particles in the ambient air of the city of Kazan. Material and methods. Long-term analysis of ambient air pollution by fine particles in the city of Kazan for the period from 2016 to 2020 has been carried out. To study the effect of separate factors (year, measurement time during the day, climatic conditions, the presence of other pollutants) on the levels of PM10 and PM2.5, regression analysis was applied based on the method of mixed models. To characterize the elemental composition of the PM2.5 fraction, sampling of atmospheric air on PVC filters was carried out by use of 100 NR impactor (TSI, USA). The step function and MPPD model were applied to calculate the number of particles and the mass of the deposited fraction of fine particulate matter in different regions of the human respiratory tract. Results. The PM10 concentrations remained stable over a 5-year period, while the PM2.5 concentrations decreased. At the same time, an increase in the maximum annual concentrations of both fractions was observed. The concentrations of PM10 and PM2.5 significantly depended on climatic conditions. The presence of nitrogen oxides and organic carbon in the ambient air was significantly associated with higher concentrations of PM10 and PM2.5. The elemental composition of PM2.5 fraction was represented mainly by carbon (C) (from 86.16% to 93.45%). Mathematical modeling has shown that PM10 is mainly deposited in the upper respiratory tract, and their presence in the tracheobronchial and alveolar zones is insignificant. PM2.5 particles reach the lower respiratory tract and alveolar area. Conclusion. A statistically significant upward long-term trend in the maximum annual ambient concentrations for both fractions of fine particles can increase health risks. Secondary pollutants (nitrogen oxides, organic carbon) are important factors for the formation of secondary particles in the ambient air. The results obtained indicate that when assessing the risks to public health, it is necessary not only to use the concentrations of fine particles in ambient air, but also to consider the degree of deposition of separate fractions in different parts of the human respiratory tract, considering the alleged pathogenesis and priority target cells characteristic of individual diseases.

Determination and Similarity Analysis of PM2.5 Emission Source Profiles Based on Organic Markers for Monterrey, Mexico

Source attribution of airborne particulate matter (PM) relies on a host of different chemical species. Organic molecular markers are a set of particularly useful marker compounds for estimating source contributions to the fine PM fraction (i.e., PM2.5). Although there are many source apportionment studies based on organic markers, these studies heavily rely on the few studies that report region-specific emission profiles. Source attribution efforts, particularly those conducted in countries with emerging economies, benefit from ad hoc information to conduct the corresponding analyses. In this study, we report organic molecular marker source profiles for PM2.5 emitted from 12 major sources types from five general source categories (meat cooking operations, vehicle exhausts, industries, biomass and trash burning, and urban background) for the Monterrey Metropolitan Area (Mexico). Source emission samples were obtained from a ground-based source-dominated sampling approach. Filter-based instruments were utilized, and the loaded filters were chemically characterized for organic markers by GC-MS. Levoglucosan and cholesterol dominate charbroiled-cooking operation sources while methoxyphenols, PAHs and hopanes dominate open-waste burning, vehicle exhaust and industrial emissions, respectively. A statistical analysis showed values of the Pearson distance < 0.4 and the similarity identity distance > 0.8 in all cases, indicating dissimilar source profiles. This was supported by the coefficient of divergence average values that ranged from 0.62 to 0.72. These profiles could further be utilized in receptor models to conduct source apportionment in regions with similar characteristics and can also be used to develop air pollution abatement strategies.

Morphological and elemental characterization of leaf-deposited particulate matter from different source types: a microscopic investigation.

Particulate matter (PM) deposition on urban green enables the collection of particulate pollution from a diversity of contexts, and insight into the physico-chemical profiles of PM is key for identifying main polluting sources. This study reports on the morphological and elemental characterization of PM2-10 deposited on ivy leaves from five different environments (forest, rural, roadside, train, industry) in the region of Antwerp, Belgium. Ca. 40,000 leaf-deposited particles were thoroughly investigated by particle-based analysis using scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM/EDX) and their physico-chemical characteristics were explored for PM source apportionment purposes. The size distribution of all deposited particles was biased towards small-sized PM, with 32% of the particles smaller than 2.5μm (PM2.5) and median diameters of 2.80-3.09μm. The source type influenced both the particles' size and morphology (aspect ratio and shape), with roadside particles being overall the smallest in size and the most spherical. While forest and rural elemental profiles were associated with natural PM, the industry particles revealed the highest anthropogenic metal input. PM2-10 profiles for roadside and train sites were rather comparable and only distinguishable when evaluating the fine (2-2.5μm) and coarse (2.5-10μm) PM fractions separately, which enabled the identification of a larger contribution of combustion-derived particles (small, circular, Fe-enriched) at the roadside compared to the train. Random forest prediction model classified the source type correctly for 61-85% of the leaf-deposited PM. The still modest classification accuracy denotes the influence of regional background PM and demands for additional fingerprinting techniques to facilitate source apportionment. Nonetheless, the obtained results demonstrate the utility of leaf particle-based analysis to fingerprint and pinpoint source-specific PM, particularly when considering both the composition and size of leaf-deposited particles.

Chromium and Zinc Speciation in Airborne Particulate Matter Collected in Ulaanbaatar, Mongolia, by X-Ray Absorption Near-edge Structure Spectroscopy

ABSTRACT This study examined the chemical speciation of atmospheric particulate matter (PM) samples collected in Ulaanbaatar, Mongolia. The health effects of atmospheric aerosol depend on the particles’ size distribution, elemental composition and chemical species as well as other factors, which vary according to the pollution sources and meteorological conditions. Employing the International Atomic Energy Agency (IAEA) supported X-ray fluorescence (XRF) beamline at Elettra Sincrotrone Trieste, Italy, we used a small incidence angle for the synchrotron emission radiation in this ultra-high-vacuum environment to analyze the fine and the coarse mode (PM2.5 and PM2.5-10, respectively) through X-ray absorption near-edge structure (XANES) spectroscopy, which was applied to the K-edges of the chromium (Cr) and zinc (Zn) in PM samples selected via energy-dispersive XRF (EDXRF) analysis for their high concentrations of these transition metals. The spectroscopic results identified trivalent chromium sulfate [Cr2(SO4)3] and chromium oxide (Cr2O3) compounds as the major chemical forms of Cr in both the coarse and the fine PM fraction. Furthermore, both fractions contained abundances of sulfate (ZnSO4) and silicate (Zn2SiO4) compounds, but only the fine mode contained Zn oxalate (ZnC2O4), whereas only the coarse mode contained Zn chloride (ZnCl2). These Cr and Zn species seemed to originate from local anthropogenic sources, e.g., combustion products or traffic-related resuspended road dust. Our findings, which are based on the first chemical speciation analysis from Ulaanbaatar, provide insight into the physiochemical characteristics of atmospheric aerosols as well as information on the potential sources of Cr and Zn species bound to fine and coarse PM.

Exploring the oxidative potential and respiratory deposition of size-segregated particulate matter at an urban site

According to the current understanding, the adverse health effects of particulate matter (PM) are produced by oxidative stress processes. Hence, the oxidative potential (OP) can be used as an exposure metric for more accurate approaches to the health response to ambient PM. This work explores the relationship between respiratory deposition of size-segregated PM and OP in the city of Santiago, Chile. Size-segregated PM samples were collected at an urban site using a Micro-Orifice Uniform Deposit Impactor (MOUDI) sampler. Dithiothreitol (DTT) loss rates were measured in aqueous PM extracts to estimate the OP for each sample. Size-segregated OP showed a bi-modal distribution with a maximum centered in the accumulation mode (0.18–3.2 μm) and other in the coarse mode (3.2–18 μm). The magnitude of the OP estimated in the accumulation mode was 2.9 ± 0.8 and 2.3 ± 0.6 times the magnitude of the OP estimated in the coarse and quasi-ultrafine mode, respectively. Respiratory deposition calculations indicated that PM3.2 (with diameter less than 3.2 μm) dominated the OP lung deposition with contributions ranging from 65 to 94% in different areas of the human respiratory tract. This was due to the deposition efficiency and greater surface area of these fractions that allowed more efficient adsorption of active redox chemical species. These results may account for the greater negative impact on the lung health of the fine fractions of PM. The characterization of the OP respiratory deposition related to different fractions of PM, can result in adequate metrics to evaluate human exposure to PM and its possible health impacts.

Spatial mapping and size distribution of oxidative potential of particulate matter released by spatially disaggregated sources

The ability of particulate matter (PM) to induce oxidative stress is frequently estimated by acellular oxidative potential (OP) assays, such as ascorbic acid (AA) and 1,4-dithiothreitol (DTT), used as proxy of reactive oxygen species (ROS) generation in biological systems, and particle-bound ROS measurement, such as 2′,7′-dichlorodihydrofluorescein (DCFH) assay. In this study, we evaluated the spatial and size distribution of OP results obtained by three OP assays (OPAA, OPDCFH and OPDTT), to qualitative identify the relative relevance of single source contributions in building up OP values and to map the PM potential to induce oxidative stress in living organisms. To this aim, AA, DCFH and DTT assays were applied to size-segregated PM samples, collected by low-pressure cascade impactors, and to PM10 samples collected at 23 different sampling sites (about 1 km between each other) in Terni, an urban and industrial hot-spot of Central Italy, by using recently developed high spatial resolution samplers of PM, which worked in parallel during three monitoring periods (February, April and December 2017). The sampling sites were chosen for representing the main spatially disaggregated sources of PM (vehicular traffic, rail network, domestic heating, power plant for waste treatment, steel plant) present in the study area. The obtained results clearly showed a very different sensitivity of the three assays toward each local PM source. OPAA was particularly sensitive toward coarse particles released from the railway, OPDCFH was sensible to fine particles released from the steel plant and domestic biomass heating, and OPDTT was quite selectively sensitive toward the fine fraction of PM released by industrial and biomass burning sources.

Mitochondrial alterations triggered by repeated exposure to fine (PM2.5-0.18) and quasi-ultrafine (PM0.18) fractions of ambient particulate matter

Nowadays ambient particulate matter (PM) levels still regularly exceed the guideline values established by World Health Organization in most urban areas. Numerous experimental studies have already demonstrated the airway toxicity of the fine fraction of PM (FP), mainly triggered by oxidative stress-induced airway inflammation. However, only few studies have actually paid close attention to the ultrafine fraction of PM (UFP), which is likely to be more easily internalized in cells and more biologically reactive. Mitochondria are major endogenous sources of reactive oxygen species (ROS) through oxidative metabolism, and coordinate many critical cellular signaling processes. Mitochondria have been often studied in the context of PM toxicity and generally associated with apoptosis activation. However, little is known about the underlying adaptation mechanisms that could occur following exposure at sub-apoptotic doses of ambient PM. Here, normal human bronchial epithelial BEAS-2B cells were acutely or repeatedly exposed to relatively low doses (5 µg.cm−2) of FP (PM2.5-0.18) or quasi-UFP (Q-UFP; PM0.18) to better access the critical changes in mitochondrial morphology, functions, and dynamics. No significant cytotoxicity nor increase of apoptotic events were reported for any exposure. Mitochondrial membrane potential (ΔΨm) and intracellular ATP content were also not significantly impaired. After cell exposure to sub-apoptotic doses of FP and notably Q-UFP, oxidative phosphorylation was increased as well as mitochondrial mass, resulting in increased production of mitochondrial superoxide anion. Given this oxidative boost, the NRF2-ARE signaling pathway was significantly activated. However, mitochondrial dynamic alterations in favor of accentuated fission process were observed, in particular after Q-UFP vs FP, and repeated vs acute exposure. Taken together, these results supported mitochondrial quality control and metabolism dysfunction as an early lung underlying mechanism of toxicity, thereby leading to accumulation of defective mitochondria and enhanced endogenous ROS generation. Therefore, these features might play a key role in maintaining PM-induced oxidative stress and inflammation within lung cells, which could dramatically contribute to the exacerbation of inflammatory chronic lung diseases. The prospective findings of this work could also offer new insights into the physiopathology of lung toxicity, arguably initiate and/or exacerbate by acutely and rather repeated exposure to ambient FP and mostly Q-UFP.

Rapid reduction in black carbon emissions from China: evidence from 2009–2019 observations on Fukue Island, Japan

Abstract. A long-term, robust observational record of atmospheric black carbon (BC) concentrations at Fukue Island for 2009–2019 was produced by unifying the data from a continuous soot monitoring system (COSMOS) and a Multi-Angle Absorption Photometer (MAAP). This record was then used to analyze emission trends from China. We identified a rapid reduction in BC concentrations of (-5.8±1.5) % yr−1 or −48 % from 2010 to 2018. We concluded that an emission change of (-5.3±0.7) % yr−1, related to changes in China of as much as −4.6 % yr−1, was the main underlying driver. This evaluation was made after correcting for the interannual meteorological variability (IAV) by using the regional atmospheric chemistry model simulations from the Weather Research and Forecasting (WRF) and Community Multiscale Air Quality (CMAQ) models (collectively WRF/CMAQ) with the constant emissions. This resolves the current fundamental disagreements about the sign of the BC emissions trend from China over the past decade as assessed from bottom-up emission inventories. Our analysis supports inventories reflecting the governmental clean air actions after 2010 (e.g., MEIC1.3, ECLIPSE versions 5a and 6b, and the Regional Emission inventory in ASia (REAS) version 3.1) and recommends revisions to those that do not (e.g., Community Emissions Data System – CEDS). Our estimated emission trends were fairly uniform across seasons but diverse among air mass origins. Stronger BC reductions, accompanied by a reduction in carbon monoxide (CO) emissions, occurred in regions of south-central East China, while weaker BC reductions occurred in north-central East China and northeastern China. Prior to 2017, the BC and CO emissions trends were both unexpectedly positive in northeastern China during winter months, which possibly influenced the climate at higher latitudes. The pace of the estimated emissions reduction over China surpasses the Shared Socioeconomic Pathways (SSPs with reference to SSP1, specifically) scenarios for 2015–2030, which suggests highly successful emission control policies. At Fukue Island, the BC fraction of fine particulate matter (PM2.5) also steadily decreased over the last decade. This suggests that reductions in BC emissions started without significant delay when compared to other pollutants such as NOx and SO2, which are among the key precursors of scattering PM2.5.