Search Results (322)

Long-term source apportionment of PM_2.5 during high-pollution periods is essential for achieving sustained reductions in both PM_2.5 levels and their health impacts. This study conducted PM_2.5 sampling in Shenzhen from January to March over the years 2021–2024 to investigate the long-term impact of coronavirus disease 2019 and the short-term impact of the Spring Festival on PM_2.5 levels. The measured average PM_2.5 concentration during the research period was 22.5 μg/m³, with organic matter (OM) being the dominant component. Vehicle emissions, secondary sulfate, secondary nitrate, and secondary organic aerosol were identified by receptor model as the primary sources of PM_2.5 during the observational periods. The pandemic led to a decrease of between 30% and 50% in the contributions of most anthropogenic sources in 2022 compared to 2021, followed by a rebound. PM_2.5 levels in January–March 2024 dropped by 1.4 μg/m³ compared to 2021, mainly due to reduced vehicle emissions, secondary sulfate, fugitive dust, biomass burning, and industrial emissions, reflecting Shenzhen’s and nearby cities’ effective control measures. However, secondary nitrate and fireworks-related emissions rose significantly. During the Spring Festival, PM_2.5 concentrations were 23% lower than before the festival, but the contributions of fireworks burning exhibited a marked increase in both 2023 and 2024. Specifically, during intense peak events, fireworks burning triggered sharp, short-term spikes in characteristic metal concentrations, accounting for over 50% of PM_2.5 on those peak days. In the future, strict control over vehicle emissions and enhanced management of fireworks burning during special periods like the Spring Festival are necessary to reduce PM_2.5 concentration and improve air quality. Full article

This study describes a quite special and interesting atmospheric event characterized by the simultaneous presence of fresh and aged smoke layers. These peculiar conditions occurred on 16 July 2024 at the CNR-IMAA atmospheric observatory (CIAO) in Potenza (Italy), and represent an ideal case for the evaluation of the impact of aging and transport mechanisms on both the optical and microphysical properties of biomass burning aerosol. The fresh smoke was originated by a local wildfire about 2 km from the measurement site and observed about one hour after its ignition. The other smoke layer was due to a wide wildfire occurring in Canada that, according to backward trajectory analysis, traveled for about 5–6 days before reaching the observatory. Synergetic use of lidar, ceilometer, radar, and microwave radiometer measurements revealed that particles from the local wildfire, located at about 3 km a.s.l., acted as condensation nuclei for cloud formation as a result of high humidity concentrations at this altitude range. Optical characterization of the fresh smoke layer based on Raman lidar measurements provided lidar ratio (LR) values of 46 ± 4 sr and 34 ± 3 sr, at 355 and 532 nm, respectively. The particle linear depolarization ratio (PLDR) at 532 nm was 0.067 ± 0.002, while backscatter-related Ångström exponent (AEβ) values were 1.21 ± 0.03, 1.23 ± 0.03, and 1.22 ± 0.04 in the spectral ranges of 355–532 nm, 355–1064 nm and 532–1064 nm, respectively. Microphysical inversion caused by these intensive optical parameters indicates a low contribution of black carbon (BC) and, despite their small size, particles remained outside the ultrafine range. Moreover, a combined use of CIAO remote sensing and in situ instrumentation shows that the particle properties are affected by humidity variations, thus suggesting a marked particle hygroscopic behavior. In contrast, the smoke plume from the Canadian wildfire traveled at altitudes between 6 and 8 km a.s.l., remaining unaffected by local humidity. Absorption in this case was higher, and, as observed in other aged wildfires, the LR at 532 nm was larger than that at 355 nm. Specifically, the LR at 355 nm was 55 ± 2 sr, while at 532 nm it was 82 ± 3 sr. The AEβ values were 1.77 ± 0.13 and 1.41 ± 0.07 at 355–532 nm and 532–1064 nm, respectively and the PLDR at 532 nm was 0.040 ± 0.003. Microphysical analysis suggests the presence of larger, yet much more absorbent particles. This analysis indicates that both optical and microphysical properties of smoke can vary significantly depending on its origin, persistence, and transport in the atmosphere. These factors that must be carefully incorporated into future climate models, especially considering the frequent occurrences of fire events worldwide. Full article

Biomass burning processes affect many semi-rural areas in the Mediterranean, but there is a lack of long-term datasets focusing on their classification, obtained by monitoring carbonaceous particle concentrations and optical properties variations. To address this issue, a campaign to measure equivalent black carbon (eBC) and particle number size distributions (0.3–10 μm) was carried out from August 2019 to November 2020 at a coastal semi-rural site in the Basilicata region of Southern Italy. Long-term datasets were useful for aerosol characterization, helping to clearly identify traffic as a constant eBC source. For a shorter period, PM_2.5 mass concentrations were also measured, allowing the estimation of elemental and organic carbon (EC and OC), and chemical and SEM (scanning electron microscope) analysis of aerosols collected on filters. This multi-instrumental approach enabled the discrimination among different biomass burning (BB) processes, and the analysis of three case studies related to domestic heating, regional smoke plume transport, and a local smoldering process. The AAE (Ångström absorption exponent) daily pattern was characterized as having a peak late in the morning and mean hourly values that were always higher than 1.3. Full article

The updated MODIS Collection 6.1 (C6.1) Dark Target (DT) aerosol optical depth (AOD) is extensively utilized in aerosol-climate studies in China. Nevertheless, the long-term accuracy of this data remains under-evaluated, especially for the forested areas. This study was undertaken to substantiate the accuracy of MODIS Terra (MOD04) and Aqua (MYD04) at 3 km resolution AOD retrievals at six forested sites in China from 2004 to 2022. The results revealed that MODIS C6.1 DT MOD04 and MYD04 datasets display good correlation (R = 0.75), low RMSE (0.20, 0.18), but significant underestimation, with only 53.57% (Terra) and 52.20% (Aqua) of retrievals within expected error (EE). Both the Terra and Aqua struggled in complex terrain (Gongga Mt.) and high aerosol loads (AOD > 1). In northern sites, MOD04 outperformed MYD04 with better correlation and a relatively high number of retrievals percentage within EE. In contrast, MYD04 outperformed MOD04 in central region with better R (0.69 vs. 0.62), and high percentage within EE (68.70% vs. 63.62%). Since both products perform well in the central region, MODIS C6.1 DT products are recommended for this region. In southern sites, MOD04 product performs relatively better than MYD04 with a marginally higher percentage within EE. However, MYD04 shows better correlation, although a higher number of retrievals fall below EE compared to MOD04. Seasonal biases, driven by snow and dust, were pronounced at northern sites during winter and spring. Southern sites faced issues during biomass burning seasons and complex terrain further degraded accuracy. MOD04 demonstrated a marginally superior performance compared to MYD04, yet both failed to achieve the global validation benchmark (66% within). The proposed results highlight critical limitations of current aerosol retrieval algorithms in forest and mountainous landscapes, necessitating methodological refinements to improve satellite-based derived AOD accuracy in ecological sensitive areas. Full article

The Metropolitan Area of Queretaro (MAQ) is a significant industrial hub in central Mexico whose air quality, including high concentrations of particulate matter (PM), poses a risk to the population. However, there have not been many studies on the sources and processes that influence the concentration of atmospheric pollutants. We used aerosol chemical composition and meteorological data from 1 January to 15 May 2022, along with back-trajectory modeling, to investigate emission sources not previously described in the region and the impact of local and regional meteorology on the chemical composition of aerosols. Furthermore, this study presents the first quantitative analysis of nitroaromatic compounds (NACs) in particulate matter in the MAQ using ultra-performance liquid chromatography coupled with high-resolution mass spectrometry. The NAC concentrations ranged from 0.086 to 3.618 ng m⁻³, with the highest concentrations occurring during a period of atmospheric stability. The secondary inorganic and organic fractions of the PM were the most abundant (50%) of the PM concentration throughout the campaign. Local and regional meteorology played a significant role in the variability of PM chemical composition, as it influenced oxidation and transport processes. The results reveal that emissions from biomass burning are a recurrent PM source, and regional emissions significantly impact the organic fraction of the PM. These results underscore the importance of considering both local and regional sources in assessing air pollution in the region. Full article

This study presents a global aerosol climatology derived from six years (October 2018–October 2024) of the Ice, Cloud, and land Elevation Satellite-2 (ICESat-2) observations, using a U-Net Convolutional Neural Network (CNN) machine learning algorithm for Cloud–Aerosol Discrimination (CAD). Despite ICESat-2’s design primarily as an altimetry mission with a single-wavelength, low-power, high-repetition-rate laser, ICESat-2 effectively captures global aerosol distribution patterns and can provide valuable insights to bridge the observational gap between the Cloud–Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) and Earth Cloud, Aerosol and Radiation Explorer (EarthCARE) missions to support future spaceborne lidar mission design. The machine learning approach outperforms traditional thresholding methods, particularly in complex conditions of cloud embedded in aerosol, owing to a finer spatiotemporal resolution. Our results show that annually, between 60°S and 60°N, 78.4%, 17.0%, and 4.5% of aerosols are located within the 0–2 km, 2–4 km, and 4–6 km altitude ranges, respectively. Regional analyses cover the Arabian Sea (ARS), Arabian Peninsula (ARP), South Asia (SAS), East Asia (EAS), Southeast Asia (SEA), the Americas, and tropical oceans. Vertical aerosol structures reveal strong trans-Atlantic dust transport from the Sahara in summer and biomass burning smoke transport from the Savanna during dry seasons. Marine aerosol belts are most prominent in the tropics, contrasting with earlier reports of the Southern Ocean maxima. This work highlights the importance of vertical aerosol distributions needed for more accurate quantification of the aerosol–cloud interaction influence on radiative forcing for improving global climate models. Full article

Medellín, a densely populated city in the Colombian Andes, faces significant health and environmental risks due to poor air quality. This is linked to the atmospheric dynamics of the valley in which it is located (Aburrá Valley). The region is characterized by a narrow valley and one of the most polluted areas in South America. This is a comparative study of the chemical composition of PM_2.5 (particles with diameter less than 2.5 µm) in Medellín between two periods (2014–2015 and 2018–2019) in which temporal trends and emission sources were evaluated. PM_2.5 samples were collected from urban, suburban, and rural stations following standardized protocols and compositional analyses of metals (ICP-MS), ions (ion chromatography), and carbonaceous species (organic carbon (OC) and elemental carbon (EC) by thermo-optical methods) were performed. The results show a reduction in average PM_2.5 concentrations for the two periods (from 26.74 µg/m³ to 20.10 µg/m³ in urban areas), although levels are still above WHO guidelines. Urban stations showed higher PM_2.5 levels, with predominance of carbonaceous aerosols (Total Carbon—TC = OC + EC = 35–50% of PM_2.5 mass) and secondary ions (sulfate > nitrate, 13–14% of PM_2.5 mass). Rural areas showed lower PM_2.5 concentrations but elevated OC/EC ratios, suggesting the influence of biomass burning as a major emission source. Metals were found to occupy fractions of less than 10% of the PM_2.5 mass; however, they included important toxic species associated with respiratory and cardiovascular risks. This study highlights progress in reducing PM_2.5 levels in the region, which has been impacted by local policies but emphasizes current and future challenges related mainly to secondary aerosol formation and carbonaceous aerosol emissions. Full article

Optical properties and chemical composition of atmospheric fine particles (PM_2.5) are critical to their environmental and health effects. In this study, we analyzed the organic aerosols (OA) in PM_2.5 samples in Nanjing, China, collected during the summer and winter of 2019 and 2023. Results show a decline in both concentrations and light-absorbing abilities of methanol—soluble organic carbon (MSOC) and water-soluble OC (WSOC) in OA from 2019 to 2023. Due to increased combustion activities, MSOC and WSOC concentrations, and their corresponding mass absorption efficiencies were all higher in winter than in summer. Furthermore, fluorescence indices suggest that OA in Nanjing was influenced by a mix of microbial/biogenic sources. Fluorescent properties of both WSOC and MSOC were dominated by humic-like components but the remaining contribution from protein-like components was more significant in MSOC. The molecular composition of OA did not show a remarkable difference between 2019 and 2023. Overall, CHON compounds were the most abundant species, followed by CHO and CHN compounds, and aliphatic compounds dominated all molecular types except for CHN (in positive mode) and CHON, CHOS (in negative mode). Regarding the OA sources, the numbers of molecules from fossil fuel combustion and biomass burning (BB) were a bit more in 2023 than in 2019, and signal intensities of BB-related molecules were also higher in winter than in summer; the presence of organosulfates indicate the contribution of aqueous-phase oxidation to OA, especially during high relative humidity conditions. At last, correlations between OA molecules and light absorption efficiencies indicate that the key light-absorbing species in winter and summer were likely quite different despite similar chemical compositions, and in summer, CH and CHN compounds were important to light absorption, whereas CHNS compounds became more important in winter. Full article

This study examines the seasonality of Black Carbon (BC) and Brown Carbon (BrC) spectral absorption characteristics at a continental background site (Kozani) in southern Balkans (NW Greece). It aims to assess the seasonality and impact of different sources on light absorption properties, BC concentrations, and the fraction of BrC absorption. Moderate-to-low BC concentrations were observed, ranging from 0.05 µg m⁻³ to 2.44 µg m⁻³ on an hourly basis (annual mean: 0.44 ± 0.27 µg m⁻³; median: 0.39 µg m⁻³) with higher levels during winter (0.53 ± 0.33), reflecting enhanced emissions from residential wood burning (RWB) for heating purposes. Atmospheric conditions are mostly clean during spring (MAM) (BC: 0.34 µg m⁻³), associated with increased rainfall. BC components associated with fossil fuel combustion (BC_ff) and biomass burning (BC_bb), maximize in summer (0.36 µg m⁻³) and winter (0.28 µg m⁻³), respectively, while the absorption Ångstrôm exponent (AAE_370–880) values ranged from 1.09 to 1.93 on daily basis. The annual mean total absorption coefficient (b_abs,520) inferred by aethalometer (AE33) was 4.09 ± 2.65 Mm⁻¹ (median: 3.51 Mm⁻¹), peaking in winter (5.30 ± 3.35 Mm⁻¹). Furthermore, the contribution of BrC absorption at 370 nm, was also high in winter (36.7%), and lower during the rest of the year (17.3–29.8%). The measuring station is located at a rural background site 4 km outside Kozani City and is not directly affected by traffic and urban heating emissions. Therefore, the regional background atmosphere is composed of a significant fraction of carbonaceous aerosols from RWB in nearby villages, a characteristic feature of the Balkan’s rural environment. Emissions from the lignin-fired power plants, still operating in the region, have decreased during the last years and moderately affect the atmospheric conditions. Full article

Nitro-functionalized heterocycles, such as nitroimidazoles, are significant environmental contaminants and have been identified as components of secondary organic aerosols (SOA) and biomass-burning organic aerosols (BBOA). Their strong absorption in the near-UV (300–400 nm) makes photochemistry a critical aspect of their atmospheric processing. This study investigates both the direct near-UV photochemistry and hydroxyl radical (OH) oxidation of 4-nitroimidazole (4-NI). The atmospheric photolysis rate of 4-NI in the near-UV (300–400 nm) was found to be J_4-NI = 4.3 × 10⁻⁵ (±0.8) s⁻¹, corresponding to an atmospheric lifetime of 391 (±77) min under bulk aqueous conditions simulating aqueous aerosols and cloud water. Electrospray ionization mass spectrometry (ESI-MS) analysis following irradiation indicated loss of the nitro group, while NO elimination was observed as a more minor channel in direct photolysis. In addition, the rate constant for the reaction of 4-NI with OH radicals, k_NI+OH, was determined to be 2.9 × 10⁹ (±0.6) M⁻¹s⁻¹. Following OH oxidation, ESI-MS results show the emergence of a dominant peak at m/z = 130 amu, consistent with hydroxylation of 4-NI. Computational results indicate that OH radical addition occurs with the lowest barrier at the C2 and C5 positions of 4-NI. The combined results from direct photolysis and OH oxidation experiments suggest that OH-mediated degradation is likely to dominate under aerosol-phase conditions, where OH radical concentrations are elevated, while direct photolysis is expected to be the primary loss mechanism in high-humidity environments and bulk cloud water. Full article

Long-term investigations of Aerosol Optical Depth (AOD) across Asia are crucial for understanding its regional impacts on the global climate system. However, satellite-derived AOD datasets frequently suffer from missing values due to factors such as cloud cover, algorithmic limitations, and various atmospheric conditions. To overcome these challenges, this study employs the deep learning model TabNet, incorporating Digital Elevation Model (DEM) data and ERA5 meteorological variables, to fuse MERRA-2 AOD with MODIS MAIAC AOD observations. The resulting integration yields a high-resolution, seamless daily AOD dataset for Asia spanning the period from 2001 to 2024. The fused dataset demonstrates significant improvements over the original MERRA-2 AOD, with an increase in the coefficient of determination (R²) by 0.1065 and a reduction in root mean square error (RMSE) by 0.0369. Spatio-temporal analysis, conducted using Empirical Orthogonal Function (EOF) decomposition, reveals that AOD concentrations across Asia are strongly influenced by anthropogenic factors, including industrial activities, transportation emissions, and biomass burning. The results indicate a generally increasing trend in AOD from 2001 to 2014, followed by a declining trend from 2015 to 2024. Notably, EOF results show a marked rise in AOD levels in Mongolia after 2020, likely attributable to an uptick in dust storm activity. This research offers valuable insights into the spatiotemporal trends of aerosols across Asia, underscoring the need for sustained air quality measures to mitigate pollution and protect public health. Full article

Biomass burning (BB) aerosols are the largest source of absorbing aerosols on Earth. Coupled with marine stratocumulus clouds (MSC), their radiative effects are enhanced and can cause cloud property changes (first indirect effect) or cloud burn-off and warm up the atmospheric column (semi-direct effect). Nevertheless, the derivation of their quantity and optical properties in the presence of MSC clouds is confounded by the uncertainties in the retrieval of the underlying cloud properties. Therefore, a robust methodology is needed for the coupled retrievals of absorbing aerosol above clouds. Here, we present a new retrieval approach implemented for a Spectro radiometric multi-angle polarimetric airborne platform, the research scanning polarimeter (RSP), during the ORACLES campaign over the Southeast Atlantic Ocean. Our approach transforms the 1D measurements over multiple angles and wavelengths into a 3D image-like input, which is then processed using various deep learning (DL) schemes to yield aerosol single scattering albedos (SSAs), aerosol optical depths (AODs), aerosol effective radii, and aerosol complex refractive indices, together with cloud optical depths (CODs), cloud effective radii and variances. We present a comparison between the different DL approaches, as well as their comparison to existing algorithms. We discover that the Vision Transformer (ViT) scheme, traditionally used by natural language models, is superior to the ResNet convolutional Neural-Network (CNN) approach. We show good validation statistics on synthetic and real airborne data and discuss paths forward for making this approach flexible and readily applicable over multiple platforms. Full article

Atmospheric aqueous-phase reactions have been recognized as an important source of secondary organic aerosols (SOAs). However, the unclear reaction kinetics and mechanics hinder the in-depth understanding of the SOA sources and formation processes. This study selected ten different substituted phenolic compounds (termed as PhCs) emitted from biomass burning as precursors, to investigate the kinetics using OH oxidation reactions under simulated sunlight. The factors influencing reaction rates were examined, and the contribution of reactive oxygen species (ROS) was evaluated through quenching and kinetic analysis experiments. The results showed that the pseudo-first-order rate constants (k_obs) for the OH oxidation of phenolic compounds ranged from 1.03 × 10⁻⁴ to 7.85 × 10⁻⁴ s⁻¹ under simulated sunlight irradiation with an initial H₂O₂ concentration of 3 mM. Precursors with electron-donating groups (-OH, -OCH₃, -CH₃, etc.) exhibited higher electrophilic radical reactivity due to the enhanced electron density of the benzene ring, leading to higher reaction rates than those with electron-withdrawing groups (-NO₂, -CHO, -COOH). At pH 2, the second-order reaction rate (k_{PhCs, OH}) was lower than at pH 5. However, the k_obs did not show dependence on pH. The presence of O₂ facilitated substituted phenols’ photodecay. Inorganic salts and transition metal ions exhibited varying effects on reaction rates. Specifically, NO₃⁻ and Cu²⁺ promoted k_{PhCs, OH}, Cl⁻ significantly enhanced the reaction at pH 2, while SO₄²⁻ inhibited the reaction. The k_{PhCs, OH} were determined to be in the range of 10⁹~10¹⁰ L mol⁻¹ s⁻¹ via the bimolecular rate method, and a modest relationship with their oxidation potential was found. Additionally, multiple substituents can suppress the reactivity of phenolic compounds toward •OH based on Hammett plots. Quenching experiments revealed that •OH played a dominant role in phenolic compound degradation (exceeding 65%). Electron paramagnetic resonance confirmed the generation of singlet oxygen (¹O₂) in the system, and probe-based quantification further explored the concentrations of •OH and ¹O₂ in the system. Based on reaction rates and concentrations, the atmospheric aqueous-phase lifetimes of phenolic compounds were estimated, providing valuable insights for expanding atmospheric kinetic databases and understanding the chemical transformation and persistence of phenolic substances in the atmosphere. Full article

Open burning of biomass has occurred around the world, and emissions from biomass burning are impacting local, regional, and global air quality issues and climate change. This study focuses on severe biomass burning aerosols (BBAs) in Sumatra in September 2019. The chemical transport simulation model employed in this study is based on a meteorological field simulated by SCALE (Scalable Computing for Advanced Library and the Environmental Regional Model) for offline calculations. Simulation results are validated by using ground-based measurements and biomass burning aerosol distribution observed by JAXA/GCOM-C (Global Change Observation Mission-Climate)/SGLI (second-generation global imager). The results of this study show that the injection process in the model simulations has a significant impact on the aerosol distribution. Aerosols generated by fires can rise to higher altitudes due to the heat of the fire, but aerosols originating from surface and soil fires were found to reproduce well at less elevated injection height. Full article

Particulate matter (PM₁₀ and PM_2.5) is a key contributor to urban air pollution and poses significant health risks, particularly in densely populated areas. While conventional air quality monitoring focuses on particle size and concentration, this study emphasizes the importance of understanding chemical composition and emission sources for effective air pollution management. PM samples were collected between 2019 and 2022 at two locations in the Republic of Slovenia: a traffic-dominated urban site and an industrial area. Annual average PM₁₀ concentrations ranged from 14 to 34 µg/m³, and those of PM_2.5 ranged from 9 to 22 µg/m³. In addition to decreasing annual concentrations, a notable reduction in exceedance days was observed between 2019 and 2022, indicating the effectiveness of recent air quality improvement measures. Meteorological data and statistical models were used to assess environmental influences on PM variability. Advanced SEM-EDS analysis revealed substantial seasonal and spatial differences in particle composition, with key elements such as silicon (4.3–28.4%), carbon (13.1–61.7%), and trace amounts of lead and zinc varying across sites and particle types. Mineral dust (Si, Al, Ca, Fe, Mg), originating from soil resuspension, construction, and Saharan dust, was dominant. Combustion-related particles containing C, Pb, Zn, and Fe oxides were associated with vehicle emissions, industrial processes, and biomass burning. Secondary aerosols, such as sulphates and nitrates, showed seasonal trends, with higher concentrations in summer and winter, respectively. The results confirm that PM levels are driven by complex interactions between local emissions, weather conditions, and seasonal dynamics. The study supports targeted policy measures, particularly regarding residential heating and traffic emissions, to improve air quality. Full article