Fraction Of Particulate Matter Research Articles

Air pollution and skin aging

Air pollution is a leading environmental health risk worldwide, with detrimental effects not only on human health but also on skin aging. This review explores the link between air pollution and skin aging, focusing on the harmful effects of particulate matter (PM) and other pollutants such as polycyclic aromatic hydrocarbons (PAHs), nitrogen oxides (NO2), and ozone (O3). These pollutants penetrate the skin, inducing oxidative stress and inflammation, which accelerates the degradation of collagen and elastin in the extracellular matrix. This contributes to premature aging, wrinkles, hyperpigmentation, and inflammatory skin conditions. The smallest fractions of PM, particularly PM2.5, are the most harmful, causing significant cellular damage. Long-term exposure to these pollutants also disrupts the skin's microbiome, leading to dysbiosis and further weakening the skin's protective barrier. Current therapeutic strategies focus on protecting the skin using antioxidants, such as Vitamin C and Vitamin E, as well as probiotics and moisturizers that support the skin's natural defenses. Sunscreens also play a vital role in protecting the skin from UV-induced oxidative stress, further mitigating pollution-related damage. This review highlights the importance of developing comprehensive skincare regimens that target both pollution-induced oxidative stress and the maintenance of a healthy skin barrier. It also emphasizes the need for further research into personalized approaches to counteract the aging effects of air pollution on the skin.

Variations of phosphorus in sediments and suspended particulate matter of a typical mesotrophic plateau lake and their contribution to eutrophication

Internal phosphorus loading (IPL), as an important part of lake phosphorus cycle and the key to solve the eutrophication problem, is still an important cause of regional and seasonal algal blooms for some mesotrophic lakes located in plateau areas. We investigated the composition, distribution of P fractions in sediments and suspended particulate matter (SPM) of Erhai Lake, southwest China, and explored the relationships between environmental variables and spatial-temporal variations of P fractions. The total P (TP) in surface sediments ranged from 817 to 1216 mg/kg, with inert Ca-P (32%) and Res-P (24%) predominating, at a moderate level. The comparison of short-term release fluxes (0.08 mg/(m2·d)) and long-term release fluxes (0.09 mg/(m2·d)) reflected that the northern region was recovering slowly from the previous P pollution. Mobile-P (the sum of loosely adsorbed P, iron bound P, and organic P) accounted for 52.3% of the TP in SPM and showed high spatial-temporal variations, which were closely related to the growth of algae throughout the investigation. The results suggested that sediments could make a sustained contribution to IPL, and that the P in SPM was highly active and significantly contributed to eutrophication in Erhai Lake especially at the time of seasonal alternations. Our data provided important theoretical bases for the relationship between internal phosphorus loading and eutrophication in plateau lakes.

Characterization of water-soluble inorganic ions and carbonaceous aerosols in the urban atmosphere in Amman, Jordan

The urban particulate matter (PM) carbonaceous and water-soluble ions were investigated in Amman, Jordan during May 2018–March 2019. The PM2.5 total carbon (TC) annual mean was 7.6 ± 3.6 μg/m3 (organic carbon (OC) 5.9 ± 2.8 μg/m3 and elemental carbon (EC) 1.7 ± 1.1 μg/m3), which was about 16.3% of the PM2.5. The PM10 TC annual mean was 8.4 ± 3.9 μg/m3 (OC 6.5 ± 3.1 μg/m3 and elemental carbon (EC) 1.9 ± 1.1 μg/m3), about 13.3% of the PM10. The PM2.5 total water-soluble ions annual mean was 7.9 ± 1.9 μg/m3 (about 16.9%), and that of the PM10 was 10.1 ± 2.8 μg/m3 (about 16.0%). The minor ions (F−, NO2−, Br−, and PO43−) constituted less than 1% in the PM fractions. The significant fraction was for SO42− (PM2.5 4.7 ± 1.6 μg/m3 (10.0%) and PM10 5.3 ± 1.9 μg/m3 (8.3%)). The NH4+ had higher amounts of PM2.5 (1.3 ± 0.6 μg/m3; 2.7%) than that PM10 (0.9 ± 0.4 μg/m3; 1.4%). During sand and dust storm (SDS) events, TC, Cl−, and NO3− were doubled in PM, SO42− did not increase significantly, and NH4+ slightly decreased. Regression analysis revealed: (1) carbonaceous aerosols come equally from primary and secondary sources, (2) about 50% of the OC came from non-combustion sources, (3) traffic emissions dominate the PM, (4) agricultural sources have a negligible effect, (5) SO42− is completely neutralized by NH4+ in the PM2.5 but there could be additional reactions involved in the PM10, and (6) (NH4)2SO4, was the major species formed by SO42−and NH4+ instead of NH4HSO4. It is recommended to perform long-term sampling and chemical speciation for the urban atmosphere in Jordan.

Seasonal and spatial variations of arsenic and its species in particulate matter in an urban environment of Brno, Czech Republic

The present paper deals with an analysis of total arsenic concentration using ICP-MS/MS and an analysis of concentration of several arsenic species, arsenite (AsIII), arsenate (AsV), monomethylarsonate (MMA), dimethylarsenite (DMA), and trimethylarsine oxide (TMAO), using HPLC-ICP-MS/MS in the PM10 fraction of airborne urban aerosol. The samples were collected during two campaigns, in the autumn of 2022 and in the winter of 2023, at three locations within the central European city of Brno, with the aim to evaluate the seasonal and spatial variations in the PM10 composition. The results confirmed only the seasonal variability in the content of the methylated arsenic species in PM10 influenced by biomethylation processes. To gain better understanding of the possible arsenic origin, a supplementary analysis of the total arsenic concentrations was performed in samples of different size fractions of particulate matter collected using ELPI + . Local emissions, including industrial activities and heating during the winter season, were suggested as the most likely predominant source contributing to the total As content in PM10.Graphical abstract

Insight into the mechanism of solution organic fractions on soot oxidation activity enhancement

The particulate matter and soluble organic fraction emitted by diesel engine are hazardous to environment and human health. Exploring the effect mechanism of soluble organic fraction on soot oxidation is beneficial for reducing the emissions. In this study, the effects of four different types of soluble organic fractions on the soot oxidation activity and physicochemical properties are investigated. The results show that the attachment of oxygen-containing soluble organic fractions enhances the soot oxidation and reduces the peak characteristic temperature. However, the low volatility soluble organic fractions without oxygen element inhibit soot oxidation. Additionally, the high volatility soluble organic fractions without oxygen element elicit limited effects on soot oxidation. the contents of aliphatic C-H functional groups, carbonyl CO functional groups, and carboxylic acid O-CO functional groups significantly increase after adding oxygen-containing soluble organic fractions, while the limited increase in functional groups is observed in soluble organic fractions without oxygen element. Solid soluble organic fractions adhere to soot particles in the form of small particles, leading a reduction in the initial particle size distribution, while liquid soluble organic fractions exhibit block and chain shapes around the soot particles, which makes the initial particle size distribution increasing. Moreover, the attachment of all soluble organic fractions disrupts the surface order of soot particle, leading to a decrease in soot graphitization. This study is beneficial for revealing the interaction mechanism between soot and soluble organic fractions.

Assessment of air quality in the Philadelphia, Pennsylvania subway.

Subways are popular and efficient modes of transportation in cities. However, people are exposed to high levels of particulate matter (PM) in subways. Subway air quality in the United States has been investigated in a few cities, but data is lacking on simultaneous measurement of several pollutants, especially ultrafine particles (UFP) and black carbon (BC), in combination with different size fractions of PM. The goals of this study are to assess air quality in a belowground subway and compare it with outdoor ambient levels, to examine temporal variability of PM in the subway, and to analyze the correlation between PM and BC. Particulate matter of varying sizes (PM1, PM2.5, PM10), UFP, and BC were measured using DustTrak, nanoparticle detector, and micro aethalometer, respectively. Measurements were made at the belowground subway platform and the aboveground street level at 15th Street subway station in Philadelphia during summer 2022. Belowground mean PM1, PM2.5, and PM10 were 112.2 ± 61.3 µg/m3, 120 ± 65.5 µg/m3, and 182.1 ± 132 µg/m3, respectively, which were 5.4, 5.7, and 7.6 times higher than the respective aboveground street levels. The UFP lung deposited surface area (LDSA) (59.4 ± 36.2 µm2/cm3) and BC (9.5 ± 5.4 μg/m3) belowground were 1.7 times and 10.7 times higher than the aboveground. The pollutant concentration varied from day-to-day on both the locations. A higher positive correlation was found between the belowground BC and PM2.5 (r = 0.51, p < 0.05) compared to the aboveground (r = 0.16, p < 0.05). This study showed high levels of particulate matter exposure at a belowground subway station in Philadelphia. Particulate matter levels were about 5 to 8 times higher at belowground subway station than the corresponding aboveground street level. Higher levels were also observed for UFP lung deposited surface area (LDSA), while black carbon levels showed the highest concentration at the belowground level by a factor of ten compared to the aboveground level. The study shows the need for air quality management at belowground subways to reduce particulate matter exposure for the commuters.

Seasonal variation of water-soluble inorganic ions and carbonaceous components of PM2.5 and PM1 in industrial and residential areas of Suizhou, China

Seasonal variations of fine particulate matter (PM) and its chemical components in Suizhou are investigated by collecting PM2.5 and PM1 samples from industrial and residential areas between March 2017 and February 2018. The findings reveal more severe PM pollution in industrial areas compared to residential areas. Concentrations and percentages of water-soluble inorganic ions (WSII) in PM are higher in spring and winter. Notably, the high levels of SO42− and NO3− in PM1-2.5 indicate that secondary transformation of SO2 and NOx significantly contribute to the rapid increase in PM1-2.5. The conversion of NO2 to NO3− is a key factor in the winter increase of mass concentrations of PM2.5 [ρ(PM2.5)], while photochemical reactions involving NO2 drive the summer increase of ρ(PM2.5). Organic carbon (OC) and elemental carbon (EC) are mainly distributed in PM1, with OC peaking in winter. Chemical fractionation of PM reveals that carbonaceous components have a greater impact on PM1 concentration than WSII, whereas WSII more significantly affects ρ(PM2.5) than carbonaceous components. The OC to EC ratio in industrial areas (2.5 ± 1.4) and residential areas (1.9 ± 0.8) suggests more prominent secondary aerosol pollution in industrial areas. Significant correlations between secondary organic carbon (SOC), SOC conversion rate (ηSOC), and concentrations of O3-8h and NO2 in Suizhou further indicate that O3 and NO2 levels in the atmosphere influence the generation of SOC and ηSOC.

Associations between Indoor and Outdoor Size-Resolved Particulate Matter in Urban Beijing: Chemical Compositions, Sources, and Health Risks

Ventilation may lead to a deterioration in indoor air quality in urban environments located close to roads. Understanding the differences in the chemical compositions of size-resolved particulate matter (PM) in indoor air and outdoor air could aid in assessing the health impacts of air in these settings and establishing relevant regulation policies. In this study, indoor and outdoor size-resolved PM was collected from an office in Beijing in summer (between 5 and 25 July 2020) and winter (between 5 and 31 January 2021). Its chemical components, including sulfate, nitrate, ammonium, chlorine, organic matter (OM), elemental carbon (EC), crustal materials (CM), and heavy metals (HM), were analyzed. The mean levels of indoor and outdoor PM2.1 and PM9 were found to be much higher than those in the guidelines for PM2.5 and PM10 outlined by the National Ambient Air Quality Standard. Moreover, the levels of PM2.1 and PM2.1–9 mass were higher outdoors than they were indoors. The size distributions of mass concentrations were shown to be bimodal, peaking at 0.43–0.65 μm and 4.7–5.8 μm, respectively. The most abundant chemicals were OM, nitrate, and sulfate for PM2.1 and OM, CM, and nitrate for PM2.1–9. We found higher percentages of sulfate, nitrate, ammonium, EC, and HM in smaller-size fractions of PM. Additionally, positive matrix factorization showed that biomass burning, secondary inorganic aerosol, coal combustion, dust, traffic, and industrial pollution were the main sources of PM during the study period. The greatest non-carcinogenic and carcinogenic hazards were found at 0.43–0.65 μm in summer and 2.1–3.3 μm in winter. Our results indicate that size-resolved PM of ambient origin may infiltrate buildings near roads to varying degrees, resulting in negative health effects.

Characterization of aerosol and its oxidative potential in a coastal semi-rural site of Southern Italy

Considering the scarce number of studies investigating the oxidative potential of PM2.5 in Italy, a measurement campaign was conducted from February 2020 to October 2020 in a coastal semi-rural site of Basilicata (Southern Italy) with the goal to characterize the fine fraction of ambient particulate matter (PM) and investigate its chemical and toxicological properties, by means of oxidative potential. Different instruments such as an automatic low-volume sampler, an aethalometer and an optical particle counter, were employed for the measurement of PM2.5 mass concentration, equivalent black carbon (eBC) concentration and absorption Ångström exponent (AAE), and particle number size distribution in 0.25–31 μm size range, respectively. 108 daily PM samples, collected on quartz fibre filters, were chemically analysed. Organic (OC) and elemental (EC) carbon content was estimated by thermo-optical transmittance technique (TOT), the concentrations of the main water-soluble ions and total elements were determined by ion chromatography and ED-XRF technique, while the oxidative potential of the water-soluble fraction was estimated through the dithiothreitol (DTT) assay. The mean value of PM2.5 mass concentration was 9.2 ± 2.5 μg/m3 and the average contribution of measured species on PM2.5 mass was 3.3% EC; 19.3% OC; 27.0% secondary inorganic aerosol (sum of SO42−, NH4+ and NO3−), and 10.2% of the other ions and elements. The OC and EC contributions to PM2.5 mass and their mean ratio (OC/EC = 6.6 ± 3.1) suggest that the site is affected by the combined contribution of traffic emissions and biomass combustion (domestic heating and agricultural activities), with the latter prevailing over the traffic, as supported by the mean AAE value of 1.3. The mean OP normalized by sampled volume, OPDTTV, was as high as 0.34 ± 0.22 nmol/min·m3, a value comparable to those recorded for PM2.5 in suburban areas of Italy. The correlation between OPDTTV and the chemical species observed in the PM2.5 samples showed a good agreement with the carbonaceous component OC (r = 0.62) and with some ions, K+ and SO42− (r = 0.60). These results identify combustion sources as the most responsible for the relatively high OPDTTV activity of PM2.5 recorded in this area.

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.

Characterization of Wildland Firefighters' Exposure to Coarse, Fine, and Ultrafine Particles; Polycyclic Aromatic Hydrocarbons; and Metal(loid)s, and Estimation of Associated Health Risks.

Firefighters' occupational activity causes cancer, and the characterization of exposure during firefighting activities remains limited. This work characterizes, for the first time, firefighters' exposure to (coarse/fine/ultrafine) particulate matter (PM) bound polycyclic aromatic hydrocarbons (PAHs) and metal(loid)s during prescribed fires, Fire 1 and Fire 2 (210 min). An impactor collected 14 PM fractions, the PM levels were determined by gravimetry, and the PM-bound PAHs and metal(loid)s were determined by chromatographic and spectroscopic methodologies, respectively. Firefighters were exposed to a total PM level of 1408.3 and 342.5 µg/m3 in Fire 1 and Fire 2, respectively; fine/ultrafine PM represented more than 90% of total PM. Total PM-bound PAHs (3260.2 ng/m3 in Fire 1; 412.1 ng/m3 in Fire 2) and metal(loid)s (660.8 ng/m3 versus 262.2 ng/m3), distributed between fine/ultrafine PM, contained 4.57-24.5% and 11.7-12.6% of (possible/probable) carcinogenic PAHs and metal(loid)s, respectively. Firefighters' exposure to PM, PAHs, and metal(loid)s were below available occupational limits. The estimated carcinogenic risks associated with the inhalation of PM-bound PAHs (3.78 × 10-9 - 1.74 × 10-6) and metal(loid)s (1.50 × 10-2 - 2.37 × 10-2) were, respectively, below and 150-237 times higher than the acceptable risk level defined by the USEPA during 210 min of firefighting activity and assuming a 40-year career as a firefighter. Additional studies need to (1) explore exposure to (coarse/fine/ultrafine) PM, (2) assess health risks, (3) identify intervention needs, and (4) support regulatory agencies recommending mitigation procedures to reduce the impact of fire effluents on firefighters.

Temporal Pattern and Profile of a Coastal‐Deep Sea Conveyor at a Marginal Deep Oligotrophic Sea

AbstractSediment trap data set and 234Th profiles (deep water excesses and deficits) reveal that particulate organic carbon (POC) export at the highly oligotrophic Levantine Sea is dominated by lateral transport from the nearby margin. These intermediate nepheloid layers (INL) operate at multi‐depth, with the silt‐to‐clay size particulate matter (PM) fraction transported at water depths of about 100–500 m, while finer fraction arrives also at deeper depths. The shallow NIL is triggered by winter storms, manipulated by coastal flash floods and shelf resuspension and assisted by cross‐shore currents, which allow the arrival of PM at a distance of 50 km within about 10 days. The deeper INL could be related to sediments initially driven to depth by density currents. Our data show that inter‐annual differences in sediment trap fluxes were related to changes in both the intensity of coastal floods and current velocity. The frequent observation of deep‐water 234Th excesses during a (relatively) low export winter (2018) is related to lessened cleansing of the water column, that is, reduced removal of fine‐grained PM by sinking coarser‐grained material. These observations highlight the importance of winter storm intensity in the POC budget of marginal seas like the Levantine Basin (LB) even in areas with limited river discharge. This further suggests that the anticipated increase in extreme weather events due to the on‐going climate change should have an impact on this coastal‐deep sea conveyor and on POC export in the LB.

Review on Sampling Methods and Health Impacts of Fine (PM2.5, ≤2.5 µm) and Ultrafine (UFP, PM0.1, ≤0.1 µm) Particles

Airborne particulate matter (PM) is of great concern in the modern-day atmosphere owing to its association with a variety of health impacts, such as respiratory and cardiovascular diseases. Of the various size fractions of PM, it is the finer fractions that are most harmful to health, in particular ultrafine particles (PM0.1; UFPs), with an aerodynamic diameter ≤ 100 nm. The smaller size fractions, of ≤2.5 µm (PM2.5; fine particles) and ≤0.1 µm (PM0.1; ultrafine particles), have been shown to have numerous linkages to negative health effects; however, their collection/sampling remains challenging. This review paper employed a comprehensive literature review methodology; 200 studies were evaluated based on the rigor of their methodologies, including the validity of experimental designs, data collection methods, and statistical analyses. Studies with robust methodologies were prioritised for inclusion. This review paper critically assesses the health risks associated with fine and ultrafine particles, highlighting vehicular emissions as the most significant source of particulate-related health effects. While coal combustion, diesel exhaust, household wood combustors’ emissions, and Earth’s crust dust also pose health risks, evidence suggests that exposure to particulates from vehicular emissions has the greatest impact on human health due to their widespread distribution and contribution to air pollution-related diseases. This article comprehensively examines current sampling technologies, specifically focusing on the collection and sampling of ultrafine particles (UFP) from ambient air to facilitate toxicological and physiochemical characterisation efforts. This article discusses diverse approaches to collect fine and ultrafine particulates, along with experimental endeavours to assess ultrafine particle concentrations across various microenvironments. Following meticulous evaluation of sampling techniques, high-volume air samplers such as the Chem Vol Model 2400 High Volume Cascade Impactor and low-volume samplers like the Personal Cascade Impactor Sampler (PCIS) emerge as effective methods. These techniques offer advantages in particle size fractionation, collection efficiency, and adaptability to different sampling environments, positioning them as valuable tools for precise characterisation of particulate matter in air quality research and environmental monitoring.

Ambient Air Quality Assessment through Air Quality Index and Air Quality Health Index for Eastern Coastal Region, Gandhidham, Gujarat, India

The impact of coastal developmental projects such as ports on regional air quality has been a matter of concern, as they are known to induce rapid industrialization and urbanization as collateral development on a long-term basis. Gandhidham-Kachchh, Gujarat, India is hub for industrialization, thus various developmental activities and port activities may release toxic gases into the environment. Thus, an attempt was made to assess the present ambient air quality in and around eastern coastal region of Gandhidham, Gujarat using Air Quality Index (AQI) and Air Quality Health Index (AQHI). The primary focus was on respirable particulate matter (PM10) and fine particulate matter (PM2.5) along with other gaseous pollutants. In total 134 samples were collected from 11 stations during January to December 2018. Sampling was carried out 24 hourly on a monthly basis. Respirable particulate matter (PM10), fine particulate matter (PM2.5), sulphur dioxide and nitrogen dioxide ranged from 29-401 µg/m3, 13-184 µg/m3, 5.9-92.6 µg/m3and 3.7-33 µg/m3, respectively. The annual mean concentrations varied from 118-227 µg/m3, 47-82 µg/m3, 10-51 µg/m3, 11-41 µg/m3 for PM10, PM2.5, sulphur dioxide and nitrogen dioxide, respectively. In most of the sampling locations both the particulate matter fractions exceeded the permissible limit as prescribed in National Ambient Air Quality Standard (NAAQS). The AQI ranged from 28 to 106, which falls under Good and Satisfactory category of pollution as per the Central Pollution Control Board (CPCB) standards except at A-11 which falls under Moderate category. The AQHI was in the range of 5.9 to 15.8, which was alarming indicating Moderate to Very Higher Risk to the people. The present findings throw light on the prevailing scenario in the ambient air quality of the studied region, thereby suggesting for strict implementation and thorough control measures for reduction of particulate matters in the air.

Prenatal and postnatal early life exposure to greenness and particulate matter of different size fractions in relation to childhood rhinitis - A multi-center study in China

The impact of early life exposure to residential greenness on childhood rhinitis and its interaction with particulate matter (PM) of different size fractions remain inconsistent. Herein, we recruited 40,486 preschool children from randomly selected daycare centers in 7 cities in China from 2019 to 2020, and estimated exposure to residential greenness by the normalized difference vegetation index (NDVI) with a 500 m buffer. Exposure to ambient PM (PM1, PM2.5, and PM10) was evaluated using a satellite-based prediction model (daily, at a resolution of 1 km × 1 km). By mixed-effect logistic regression, NDVI values during pregnancy, in the first (0–1 year old) and the second (1–2 years old) year of life were negatively associated with lifetime rhinitis (LR) and current rhinitis (CR) (P < 0.001). PM in the same time windows was associated with increased risks of LR and CR in children, with smaller size fraction of PM showing greater associations. The negative associations between prenatal and postnatal NDVI and LR and CR in preschool children remained robust after adjusting for concomitant exposure to PM, whereas the associations of postnatal NDVI and rhinitis showed significant interactions with PM. At lower levels of PM, postnatal NDVI remained negatively associated with rhinitis and was partly mediated by PM (10.0–40.9 %), while at higher levels of PM, the negative associations disappeared or even turned positive. The cut-off levels of PM were identified for each size fraction of PM. In conclusion, prenatal exposure to greenness had robust impacts in lowering the risk of childhood rhinitis, while postnatal exposure to greenness depended on the co-exposure levels to PM. This study revealed the complex interplay of greenness and PM on rhinitis in children. The exposure time window in prenatal or postnatal period and postnatal concomitant PM levels played important roles in influencing the associations between greenness, PM and rhinitis.

Analysis of Particulate Matter Fraction in Residential Area of Lahore, Pakistan

Analysis of Particulate Matter Fraction in Residential Area of Lahore, Pakistan

The explainable potential of coupling hybridized metaheuristics, XGBoost, and SHAP in revealing toluene behavior in the atmosphere

Toluene is a neurotoxic aromatic hydrocarbon and one of the major representatives of volatile organic compounds, known for its abundance, adverse health effects, and role in the formation of other atmospheric pollutants like ozone. This research introduces the enhanced version of the reptile search metaheuristics algorithm which has been utilized to tune the extreme gradient boosting hyperparameters, to investigate toluene atmospheric behavior patterns and interactions with other polluting species within defined environmental conditions. The study is based on a two-year database encompassing concentrations of inorganic gaseous contaminants every hour (NO, NO2, NOx, and O3), particulate matter fractions (PM1, PM2.5, and PM10), m,p-xylene, toluene, benzene, total non-methane hydrocarbons, and meteorological data. The experimental outcomes were validated against the results of extreme gradient boosting models optimized by seven other recent powerful metaheuristics algorithms. The best-performing model has been interpreted by employing Shapley additive explanations method. In the study, we have focused on the relationship between toluene and benzene, as its most important predictor, and provided a detailed description of environmental conditions which directed their interactions.

Particle emissions from heated tobacco products.

This study determines the particle emissions from five heated tobacco products (HTPs). An aethalometer is used for the determination of black carbon (BC) and an aerosol monitor for total particulate matter (PM) concentration and also PM fractions (1, 2.5, 4, and 10 μm) in the mainstream emissions of 5 HTPs: IQOS, LIL, PULZE, ILUMA, and GLO. Fifteen different flavors were used, five sticks per flavor, which were smoked using a peristaltic pump under both ISO and Canadian smoking regimes. The method repeatability was determined using 15 sticks of one flavor for each brand for each smoking regime. All HTPs emit particles, and more than 99.7% of the particles emitted are smaller than 1 μm. Both BC and PM emissions show quite low repeatability. Particle emissions increase in relation to the heating temperature and the intensity smoking regime, and are depending on the flavor used. BC corresponds to a small percentage of total PM. Although HTPs are promoted as products of reduced risk compared to conventional cigarettes, high particle concentrations are detected in their emissions, depending on the smoking regime, the flavor used, and the operation parameters. PM emissions vary significantly between different brands under the ISO smoking regime, probably due to the heating temperature. In contrast, PM emissions under the Canadian smoking regime do not vary significantly between different brands. This could probably be attributed to the fact that increased puff frequency does not allow the device to cool down between puffs, resulting in an increase in PM emissions for all the brands, but not dependent on the maximum heating temperature of the device. BC emissions only consist of a very small fraction of PM and do not vary significantly between different brands under both smoking regimes.

Assessment of seasonal variations in particulate matter accumulation and elemental composition in urban tree species

Outdoor air pollution in urban areas, especially particulate matter (PM), is harmful to human health. Urban trees and shrubs provide crucial ecosystem services such as air pollution mitigation by acting as natural filters. However, urban greenery comprises a particular biodiversity, and different plant species vary in their capacity to accumulate PM. Twenty-two plant species were analyzed and selected according to their leaf traits, the different fractions of PM accumulated on the leaves (large - PML, coarse - PMC, and fine - PMF) and their chemical composition. The study was conducted in four city zones: urban traffic (UT), urban background (UB), industrial (IND), and rural (RUR), comparing winter (W) and summer (S) seasons. The average PM levels in the air and accumulated on the leaves were higher in W than in S season. During both seasons, the highest PM accumulated on the leaves was recorded at the UT zone. Nine species were selected as the most suitable for accumulating PML, seven as the most efficient for accumulating PMC, and six for accumulating PMF. The leaf area and leaf roundness were correlated negatively with PM accumulation. The evergreen species L. nobilis was indicated as suitable for dealing with air pollution based on PM10 and PM2.5 values recorded in the air. Regarding the PM element and metal composition, L. nobilis, Photinia x fraseri, Olea europaea, Quercus ilex and Nerium oleander were selected as species with notable elements and metal accumulation. In summary, the study identified species with higher PM accumulation capacity and assessed the seasonal PM accumulation patterns in different city zones, providing insights into the species interactions with PM and their potential for monitoring and coping with air pollution.

Source attribution of carbonaceous fraction of particulate matter in the urban atmosphere based on chemical and carbon isotope composition

Air quality is of large concern in the city of Krakow, southern Poland. A comprehensive study was launched by us in which two PM fractions (PM1 and PM10) were sampled during 1-year campaign, lasting from April 21, 2018 to March 19, 2019. A suite of modern analytical methods was used to characterize the chemical composition of the collected samples. The contents of 14 sugars, sugar alcohols and anhydrosugars, 16 polycyclic aromatic hydrocarbons, selected metals and non-metals and ions were analyzed, in addition to organic and elemental carbon content. The carbon isotope composition in both analysed PM fractions, combined with an isotope-mass balance method, allowed to distinguish three main components of carbonaceous emissions in the city: (1) emissions related to combustion of hard coal, (2) emissions related to road transport, and (3) biogenic emissions. The heating season emissions from coal combustion had the biggest contribution to the reservoir of carbonaceous aerosols in the PM10 fraction (44%) and, together with the biogenic emission, they were the biggest contributors to the PM1 fraction (41% and 44%, respectively). In the non-heating season, the dominant source of carbon in PM10 and PM1 fraction were the biogenic emissions (48 and 54%, respectively).