Biomass Burning Events Research Articles

Long-range transport of air pollutants increases the concentration of hazardous components of PM2.5 in northern South America

Abstract. Long-range transport (LRT) of air pollutants from a range of sources can substantially enhance background pollution levels, especially in urbanized regions, which can exacerbate high-pollution episodes. In the Aburrá Valley (AV), Colombia, and other cities in northern South America, biomass burning (BB), dust, and volcanic degassing have been identified as sources of long-range aerosol transport. However, the impact of these sources on air quality and the characterization of these sources have yet to be thoroughly studied. This work investigates the influence of these sources on the chemical composition of PM2.5 during annual and intra-annual high-load aerosol events in the AV. We identified, tracked, and meteorologically characterized LRT events and evaluated their influence on PM2.5 concentration and chemical composition. We found that the LRT of aerosols from BB, dust, and volcanic degassing influenced approximately 13 %, 8 %, and 13 % of days in the year, respectively. We applied the positive-matrix-factorization (PMF) statistical model to quantify PM2.5 concentrations and chemical compositions for the different LRT event types (e.g., BB). For BB events, we identified large contributions from organic carbon (OC1 and OC2), F−, and secondary aerosol tracers (SO42- and NO3-). For dust LRT events, crustal mineral components, along with Ti and Ca, were the primary contributors to aerosol composition, while SO42-, Na, Al, and Ca were the primary contributors during volcanic events. The concentrations of some ions and toxic heavy metals (Cr, Mn, Cd, and Ni) were also elevated during BB and volcanic-degassing events. BB contributed the most to PM2.5 levels during the LRT events (∼11 µg m−3), while contributions from aerosols arising from dust and volcanic events were also substantial (<7 µg m−3). Our study identifies the Orinoco and the Middle Magdalena Valley as sizable sources of BB aerosols and Nevado del Ruiz as a source of volcanic aerosols. Additionally, we found that African dust reached the Andean region via the Caribbean route. As a result, we identify the need for future chemical-transport modeling studies in the region and new support strategies to manage internal and external pollution sources that degrade air quality in the AV and the surrounding region.

Impact of biomass burning on air quality: A case study of the agricultural region in South Korea

Various combustion processes occur concurrently during biomass burning events, emitting a complex mixture of particulate and gaseous pollutants into the atmosphere. These emissions undergo chemical transformations facilitated by factors such as solar radiation and cloud formation, thereby altering the composition of aerosols. Additionally, these pollutants can affect the region of origin and neighboring countries, presenting regional and global environmental challenges. Therefore, precise evaluation of the particulate and gaseous pollutants emitted during biomass burning is essential to formulate effective management strategies. This study aimed to assess the concentration and chemical characteristics of particulate matter emitted during biomass burning in South Korea. On June 7, 2021, a research flight was conducted utilizing a High Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) and a Single Particle Soot Photometer (SP2) for airborne measurements over South Korea inland areas. For data analysis based on administrative regions, the flight path was divided into four major areas (Areas A, B, C, and D). During the research flight, evidence of biomass burning events was observed primarily in Area C. A positive matrix factorization (PMF) analysis categorized the organic aerosols (OA) into five factors: biomass burning OA (BBOA), hydrocarbon-like OA (HOA1, HOA2), low-oxidized oxygenated OA (LO-OOA), and more-oxidized OOA (MO-OOA). Across all areas, MO-OOA accounted for the highest proportion of aerosols, whereas BBOA dominated in Area C at 23.8%, indicating the significant influence of biomass burning in this region. Instead of running a PMF analysis with all measurement data, a BBOA formula was derived from the previous study and this one. This allows us to estimate BBOA concentration without running PMF.

Occurrence, abundance, and formation of atmospheric tarballs from a wide range of wildfires in the western US

Abstract. Biomass burning emits large numbers of organic aerosol particles, a subset of which are called tarballs (TBs). TBs possess a spherical morphology and unique physical, chemical, and optical properties. They are recognized as brown-carbon aerosol particles, influencing the climate through the absorption of solar radiation. Aerosol particles were collected from wildfire and agricultural-fire smoke sampled by NASA's DC-8 aircraft during the Fire Influence on Regional to Global Environments and Air Quality (FIREX-AQ) campaign in the western US from July to September 2019. This study developed an image analysis method using deep learning to distinguish TBs from other round particles that deformed on the substrate, based on the particles' morphological characteristics in transmission electron microscopy images. This study detected 4567 TBs, with most occurring < 10 h downwind of the emissions, and measured their compositions, abundance, sizes, and mixing states. The number fraction, mass fraction, and concentration of TBs in wildfire smoke corresponded to 10 ± 1 %, 10 ± 2 %, and 10.1 ± 4.6 µg m−3, respectively. As the smoke aged for up to 5 h after emission, the TB number fractions roughly increased from 5 % to 15 %, indicating that TBs are processed primary particles. We also observed TBs associated with pyrocumulonimbus (pyroCb) activity and various TB mixing states. This study reveals the abundance, as well as the physical and chemical properties, of a wide range of TBs from various biomass-burning events and enhances our knowledge of TB emissions, contributing to the evaluation of the climate impact of TBs.

The Long-Term Monitoring of Atmospheric Polychlorinated Dibenzo-p-Dioxin Dibenzofurans at a Background Station in Taiwan during Biomass Burning Seasons in El Niño and La Niña Events

To measure the long-range transport of PCDD/Fs, a background sampling site at Mt. Lulin station (Taiwan) was selected based on meteorological information and its location relative to burning events in Southeast Asia. During regular sampling periods, a higher concentration of PCDD/Fs was recorded in 2008 at Mt. Lulin station during La Niña events, with levels reaching 390 fg I-TEQ/m3. In contrast, a higher concentration of 483 fg I-TEQ/m3 was observed in 2013 during biomass burning events. This indicates that La Niña affects the ambient PCDD/F concentrations. The ratio of ΣPCDD/ΣPCDF was 0.59, suggesting significant long-range transport contributions from 2007 to 2023. From 2007 to 2015, the predominant species was 2,3,4,7,8-PCDF, accounting for 25.3 to 39.6% of the total PCDD/Fs. From 2018 onward, 1,2,3,7,8-PCDD became more dominant, accounting for 15.0 to 27.1%. According to the results from the receptor model PMF (n = 150), the sources of PCDD/Fs were identified as dust storms and monsoon events (19.3%), anthropogenic activity (28.5%), and biomass burning events (52.2%). The PSCF values higher than 0.7 highlighted potential PCDD/F emission source regions for Mt. Lulin during biomass burning events, indicating high PSCF values in southern Thailand, Cambodia, and southern Vietnam.

Measurement report: Combined use of MAX-DOAS and AERONET ground-based measurements in Montevideo, Uruguay, for the detection of distant biomass burning

Abstract. Biomass burning releases large amounts of aerosols and chemical species into the atmosphere, representing a major source of air pollutants. Emissions and by-products can be transported over long distances, presenting challenges in quantification. This is mainly done using satellites, which offer global coverage and data acquisition for places that are difficult to access. In this study, ground-based observations are used to assess the abundance of trace gases and aerosols. On 24 November 2020, a significant increase in formaldehyde was observed with a Multi-AXis Differential Optical Absorption Spectroscopy (MAX-DOAS) instrument located in Montevideo (Uruguay), and its vertical column densities reached values of 2.4×1016 molec. cm−2, more than twice the values observed during the previous days. This was accompanied by an increase in the aerosol levels measured by an AErosol RObotic NETwork (AERONET) photometer located at the same site. The aerosol optical depth (AOD) at 440 nm reached values close to 1, an order of magnitude larger than typical values in Montevideo. Our findings indicate that the increase was associated with the passage of a plume originating from distant biomass burning. This conclusion is supported by TROPOspheric Monitoring Instrument (TROPOMI) satellite observations as well as HYbrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) simulations. The profiles of the gases and aerosols retrieved from the MAX-DOAS observations are consistent with the HYSPLIT analysis, showing the passage of a plume over Montevideo on 24 November located at a height of ∼ 1.5 km. This corroborates the finding that biomass burning events occurring about 800 km north of Montevideo can affect the local atmosphere through long-distance emissions transport. This study underscores the potential of ground-based atmospheric monitoring as a tool for detection of such events. Furthermore, it demonstrates greater sensitivity compared to satellite when it comes to detection of relatively small amounts of carbonyls like glyoxal and formaldehyde.

Impact of Biomass Burning, Wildfires, and Wind Events on Aerosol Optical Depth: Implications for Climate Change

In this article, we describe multiannual variations of the atmospheric aerosol optical depth values in the widely understood area of the Baltic Sea. We present the trends in the changes and depict unusual aerosol situations. As a result of analyses, we focus on 2019, since unusually high values of aerosol optical depth were recorded in several stations around the Baltic. We match the high aerosol levels with an unusually high number of wildfires across Europe in spring and summer, which emitted large quantities of aerosols into the atmosphere that were distributed over vast European areas in part by the wind. We then connect this case with the climate change consequences. Since aerosols influence the radiative budget of the planet by directly affecting the atmospheric radiation budget, it is obvious that human well-being is in danger due to wildfires, as well as from the atmospheric perspective. Climate change will lead to more frequent fires; thus, humans need to develop solutions to decrease the risk of fire outbreaks.

Short-term associations of PM10 attributed to biomass burning with respiratory and cardiovascular hospital admissions in Peninsular Malaysia.

Biomass burning (BB) is a major source of air pollution and particulate matter (PM) in Southeast Asia. However, the health effects of PM smaller than 10 µm (PM10) originating from BB may differ from those of other sources. This study aimed to estimate the short-term association of PM10 from BB with respiratory and cardiovascular hospital admissions in Peninsular Malaysia, a region often exposed to BB events. We obtained and analyzed daily data on hospital admissions, PM10 levels and BB days from five districts from 2005 to 2015. We identified BB days by evaluating the BB hotspots and backward wind trajectories. We estimated PM10 attributable to BB from the excess of the moving average of PM10 during days without BB hotspots. We fitted time-series quasi-Poisson regression models for each district and pooled them using meta-analyses. We adjusted for potential confounders and examined the lagged effects up to 3 days, and potential effect modification by age and sex. We analyzed 210960 respiratory and 178952 cardiovascular admissions. Almost 50% of days were identified as BB days, with a mean PM10 level of 53.1 µg/m3 during BB days and 40.1 µg/m3 during normal days. A 10 µg/m3 increment in PM10 from BB was associated with a 0.44% (95% CI: 0.06, 0.82%) increase in respiratory admissions at lag 0-1, with a stronger association in adults aged 15-64 years and females. We did not see any significant associations for cardiovascular admissions. Our findings suggest that short-term exposure to PM10 from BB increased the risk of respiratory hospitalizations in Peninsular Malaysia.

Characterizing Dust and Biomass Burning Events from Sentinel-2 Imagery

The detection and evaluation of biomass burning and dust events are critical for understanding their impact on air quality, climate, and human health, particularly in the Mediterranean region. This research pioneers an innovative methodology that uses Sentinel-2 multispectral (MS) imagery to meticulously pinpoint and analyze long-transport dust outbreaks and biomass burning phenomena, originating both locally and transported from remote areas. We developed the dust/biomass burning (DBB) composite normalized differential index, a tool that identifies clear, dusty, and biomass burning scenarios in the selected region. The DBB index jointly employs specific Sentinel-2 bands: B2-B3-B4 for visible light analysis, and B11 and B12 for short-wave infrared (SWIR), exploiting the specificity of each wavelength to assess the presence of different aerosols. A key feature of the DBB index is its normalization by the surface reflectance of the scene, which ensures independence from the underlying texture, such as streets and buildings, for urban areas. The differentiation involves the comparison of the top-of-atmosphere (TOA) reflectance values from aerosol events with those from clear-sky reference images, thereby constituting a sort of calibration. The index is tailored for urban settings, where Sentinel-2 imagery provides a decametric spatial resolution and revisit time of 5 days. The average values of DBB achieve a 96% match with the coarse-mode aerosol optical depths (AOD), measured by a local station of the AERONET network of sun-photometers. In future studies, the map of DBB could be integrated with that achieved from Sentinel-3 images, which offer similar spectral bands, albeit with much less fine spatial resolution, yet benefit from daily coverage.

Geostationary aerosol retrievals of extreme biomass burning plumes during the 2019–2020 Australian bushfires

Abstract. Extreme biomass burning (BB) events, such as those seen during the 2019–2020 Australian bushfire season, are becoming more frequent and intense with climate change. Ground-based observations of these events can provide useful information on the macro- and micro-physical properties of the plumes, but these observations are sparse, especially in regions which are at risk of intense bushfire events. Satellite observations of extreme BB events provide a unique perspective, with the newest generation of geostationary imagers, such as the Advanced Himawari Imager (AHI), observing entire continents at moderate spatial and high temporal resolution. However, current passive satellite retrieval methods struggle to capture the high values of aerosol optical thickness (AOT) seen during these BB events. Accurate retrievals are necessary for global and regional studies of shortwave radiation, air quality modelling and numerical weather prediction. To address these issues, the Optimal Retrieval of Aerosol and Cloud (ORAC) algorithm has used AHI data to measure extreme BB plumes from the 2019–2020 Australian bushfire season. The sensitivity of the retrieval to the assumed optical properties of BB plumes is explored by comparing retrieved AOT with AErosol RObotic NETwork (AERONET) level-1.5 data over the AERONET site at Tumbarumba, New South Wales, between 1 December 2019 at 00:00 UTC and 3 January 2020 at 00:00 UTC. The study shows that for AOT values > 2, the sensitivity to the assumed optical properties is substantial. The ORAC retrievals and AERONET data are compared against the Japan Aerospace Exploration Agency (JAXA) Aerosol Retrieval Product (ARP), Moderate Resolution Imaging Spectroradiometer (MODIS) Deep Blue over land, MODIS MAIAC, Sentinel-3 SYN and VIIRS Deep Blue products. The comparison shows the ORAC retrieval significantly improves coverage of optically thick plumes relative to the JAXA ARP, with approximately twice as many pixels retrieved and peak retrieved AOT values 1.4 times higher than the JAXA ARP. The ORAC retrievals have accuracy scores of 0.742–0.744 compared to the values of 0.718–0.833 for the polar-orbiting satellite products, despite successfully retrieving approximately 28 times as many pixels over the study period as the most successful polar-orbiting satellite product. The AHI and MODIS satellite products are compared for three case studies covering a range of BB plumes over Australia. The results show good agreement between all products for plumes with AOT values ≤ 2. For extreme BB plumes, the ORAC retrieval finds values of AOT > 15, significantly higher than those seen in events classified as extreme by previous studies, although with high uncertainty. A combination of hard limits in the retrieval algorithms and misclassification of BB plumes as cloud prevents the JAXA and MODIS products from returning AOT values significantly greater than 5.

Predicted Concentrations and Optical Properties of Brown Carbon from Biomass Burning over Europe.

Black carbon (BC) and brown carbon (BrC) are light-absorbing carbonaceous aerosol components that can contribute to radiative forcing and thus affect the climate. In this study, we focus on the modification of aerosol optical properties associated with BrC emissions from biomass burning. BrC is simulated with the introduction of three new species in the three-dimensional chemical transport model PMCAMx-SR, two primary-absorbing (inert and reactive BrC) species, and one "photobleached" BrC species. 10% of the emitted BrC is assumed to be inert, and the rest to be reactive and able to undergo photobleaching. The scattering and absorption coefficients of the aerosol for different wavelengths are estimated by using Mie theory. BrC causes a 5-15% increase of the aerosol optical depth at 550 nm in regions affected by fires and can increase light absorption by up to 12% compared to when there is no BrC. During major biomass burning events, the absorption of BrC can reach up to 13% of that of BC at 550 nm and 25% at 440 nm. The ability of the model to reproduce measured absorption is improved when BrC is added to the light-absorbing components.

Water and methanol soluble aerosol brown carbon over Bhopal, central India – Changes in optical properties and radiative effects during the COVID-19 lockdowns

Water-soluble organic carbon (WSOC) and methanol-soluble organic carbon (MeS-OC) in ambient PM2.5 over Bhopal, central India, were optically characterized during the COVID-19 lockdowns year (2020) to assess the influence of source reductions on these species and the induced changes in their radiative effects. During the lockdowns (23 March – May 31, 2020), the light absorption coefficients (babs-405) of WSOC and MeS-OC had higher values (75 %–105 %) compared to the corresponding period in 2019. MeS-OC light absorption at 365 nm and 550 nm were about thrice and twice, respectively, compared to WSOC absorption at these wavelengths. Increased fire counts and higher MAC405 (Mass Absorption Cross-section) of MeS-OC and WSOC (8 %–58 %) during the lockdowns compared to the corresponding period in 2019, indicated frequent biomass burning events because vehicular and industrial sources were completely shutdown during this period. Fractional solar radiation absorption (f300–400 nm) by MeS-OC and WSOC normalized by EC absorption was higher (15 % ± 9 % and 9 % ± 4 %, respectively) during the lockdowns compared to the corresponding period in 2019. The SFE300–400nm (Simple Forcing Efficiency) values for MeS-OCthisstudy→literature and WSOCthis study→literature were 8 % ± 5 % and 13 % ± 5 % higher, respectively, during lockdowns compared to the same period in 2019. Overall, the results suggested that biomass burning emissions during COVID-19 lockdowns offset (and overtook) any source emissions reduction induced aerosol radiative heating gains.

Distribution of ozone, carbon monoxide and oxides of nitrogen over an urban location in the foothills of the North-Western Himalayas

Increasing anthropogenic activities and biomass burning events over the Northern Indian region severely affect the pristine environment of North-Western Himalayas. To investigate their influence in this data sparse region, continuous monitoring of O3, CO and NOx are made during January 2018 to December 2019 over Dehradun, an urban location in the foothills of North-western Himalayas. Ozone shows daytime broad peak and CO and NOx show two peaks during morning and evening hours. The maximum daytime ozone is observed during spring with 58.2 ± 2.0 ppbv (56.2 ± 2.7 ppbv) during 2018 (2019). CO and NOx show maximum value during winter and minimum during summer-monsoon. Their concentrations are found to be influenced from stubble burning and forest fire emissions during late spring. WRF-Chem simulations are made with and without biomass burning emissions to quantify the contribution of these emissions on the variability of these gases over Dehradun. Sensitivity simulations reveal that biomass burning over northern Indian region contributed 43 ppbv, 79 ppbv and 1.2 ppbv increase in O3, CO and NOx mixing ratios over Dehradun. In addition, dust storm event in June 2018 contributed for lower ozone levels in 2018 (16.1 ± 9.3 ppbv) and stratosphere troposphere exchange process enhanced surface ozone in June 2019 (53.6 ± 22.3 ppbv).

Modeling the molecular composition of secondary organic aerosol under highly polluted conditions: A case study in the Yangtze River Delta Region in China

A near-explicit mechanism, the master chemical mechanism (MCMv3.3.1), coupled with the Community Multiscale Air Quality (CMAQ) model (CMAQ-MCM-SOA), was applied to investigate the characteristics of secondary organic aerosol (SOA) during a pollution event in the Yangtze River Delta (YRD) region in summer 2018. Model performances in predicting explicit volatile organic compounds (VOCs), organic aerosol (OA), secondary organic carbon (SOC), and other related pollutants in Taizhou, as well as ozone (O3) and fine particulate matter (PM2.5) in multiple cities in this region, were evaluated against observations and model predictions by the CMAQ model coupled with a lumped photochemical mechanism (SAPRC07tic, S07). MCM and S07 exhibited similar performances in predicting gaseous species, while MCM better captured the observed PM2.5 and inorganic aerosols. Both models underpredicted OA concentrations. When excluding data during biomass burning events, SOC concentrations were underpredicted by the CMAQ-MCM-SOA model (−28.4 %) and overpredicted by the CMAQ-S07 model (134.4 %), with better agreement with observations in the trend captured by the CMAQ-MCM-SOA model. Dicarbonyl SOA accounted for a significant fraction of total SOA in the YRD, while organic nitrates originating from aromatics were the most abundant species contributing to the SOA formation from gas-particle partitioning. The oxygen-to‑carbon ratio (O/C) for SOA and OA were 0.68–0.75 and 0.20–0.65, respectively, indicating a higher oxidation state in the areas influenced by biogenic emissions. Finally, the phase state of SOA was examined by calculating the glass transition temperature (Tg) based on its molecular composition. It was found that semi-solid state characterized SOA in the YRD, which could potentially impact their chemical transformation and lifetimes along with those of their precursors.

Australian Black summer smoke signal on Antarctic aerosol collected between New Zealand and the Ross sea

Open biomass burning (BB) events are a well-known primary aerosol source, resulting in the emission of significant amount of gaseous and particulate matter and affecting Earth's radiation budget. The 2019–2020 summer, known as “Australian Black Summer”, showed exceptional duration and intensity of seasonal wildfires, triggered by high temperatures and severe droughts. Since increasing megafires are predicted due to expected climate changes, it is critical to study the impact of BB aerosol on a large scale and evaluate related transport processes. In this study, five aerosol samples (total suspended particles with a diameter >1 μm) were collected during the XXXV Italian Expedition in Antarctica on board of the R/V Laura Bassi from 6th of January to February 16, 2020, along the sailing route from Lyttelton harbor (New Zealand) to Terra Nova Bay (Antarctica). Levoglucosan and its isomers have been analyzed as markers of BB, together with polycyclic aromatic hydrocarbons (PAHs), sucrose and alcohol sugars. Ionic species and carboxylic acids have been analyzed to support the identification of aerosol sources and its aging. Results showed high levoglucosan concentrations (325–1266 pg m−3) during the campaign, suggesting the widespread presence of smoke in the region, because of huge wildfire releases. Backward trajectories indicated the presence of long-range atmospheric transport from South America, probably carrying wildfires plume, in agreement with literature. Regional sources have been suggested for PAHs, particularly for 3–4 rings' compounds; monosaccharides, sucrose, arabitol, and mannitol were related to marine and biogenic contributions. In a warming climate scenario, more frequent and extensive wildfire episodes are expected in Australia, potentially altering albedo, aerosol radiative properties, and cloud interactions. Therefore, it is crucial to strengthens the investigations on the regional climatic effects of these events in Antarctica.

Impact of Biomass Burning on Arctic Aerosol Composition.

Emissions from biomass burning (BB) occurring at midlatitudes can reach the Arctic, where they influence the remote aerosol population. By using measurements of levoglucosan and black carbon, we identify seven BB events reaching Svalbard in 2020. We find that most of the BB events are significantly different to the rest of the year (nonevents) for most of the chemical and physical properties. Aerosol mass and number concentrations are enhanced by up to 1 order of magnitude during the BB events. During BB events, the submicrometer aerosol bulk composition changes from an organic- and sulfate-dominated regime to a clearly organic-dominated regime. This results in a significantly lower hygroscopicity parameter κ for BB aerosol (0.4 ± 0.2) compared to nonevents (0.5 ± 0.2), calculated from the nonrefractory aerosol composition. The organic fraction in the BB aerosol showed no significant difference for the O:C ratios (0.9 ± 0.3) compared to the year (0.9 ± 0.6). Accumulation mode particles were present during all BB events, while in the summer an additional Aitken mode was observed, indicating a mixture of the advected air mass with locally produced particles. BB tracers (vanillic, homovanillic, and hydroxybenzoic acid, nitrophenol, methylnitrophenol, and nitrocatechol) were significantly higher when air mass back trajectories passed over active fire regions in Eastern Europe, indicating agricultural and wildfires as sources. Our results suggest that the impact of BB on the Arctic aerosol depends on the season in which they occur, and agricultural and wildfires from Eastern Europe have the potential to disturb the background conditions the most.

A biogenic organic molecule involved in the formation of secondary organic aerosols: Microwave and millimeter-wave spectroscopy of 3-methylcatechol backed by quantum chemistry

3-methylcatechol (3MC) is a molecule of environmental interest due to its presence in the atmosphere during biomass burning events, leading to the formation of secondary organic aerosols. This paper goes one step further than the paper from A.S. Hazrah et al. (2022) [10]. A three-dimensional torsional potential energy surface was determined, confirming the existence of three rotamers for 3MC. One dimensional potential energy curves along the rotation of the methyl group were computed and fitted to estimate the barrier height in each conformer. Experiments were performed at low temperature in the microwave domain (2−20GHz range) and, for the first time, in the millimeter-wave domain (70−110GHz range) at T=323K with a specially designed heated absorption cell. The rotational linelist was fitted to provide updated spectroscopic parameters for the two 3MC conformers of lowest energies. In particular, the A−E splitting is observed in the microwave region for both conformers while in the millimeter-wave region, it is only seen for the conformer of the lowest energy.

Morphological and optical properties of carbonaceous aerosol particles from ship emissions and biomass burning during a summer cruise measurement in the South China Sea

Abstract. Carbonaceous aerosols constitute a crucial component of atmospheric marine aerosols among which black carbon (BC) and brown carbon (BrC) are important contributors to light absorption and hence the positive climatic radiative forcing in the marine atmosphere. We conducted month-long (5 May–9 June 2021) onboard sample collections and online measurements of carbonaceous aerosols to characterize their morphological and optical properties during a ship cruise in the South China Sea (SCS), covering a marine region of 11.9–24.5° N, 111.1–118.2° E. Single particles were collected by a single-particle sampler, and offline analyses were performed using a transmission electron microscope (TEM) coupled with energy-dispersive X-ray spectroscopy (EDS). Online measurements of BC in PM2.5 were made by a seven-wavelength aethalometer, and organic carbon (OC) and elemental carbon (EC) mass concentrations were measured by a semi-online OC/EC analyzer. Feret diameters of the single particles during navigation and stop showed size distributions with the lognormal fitting peaks at 307 and 325 nm, respectively. The fresh (without coating) and aged BC particles (after removal of coating by the electron beams in the TEM) showed same median fractal dimensions (1.61), in contrast to their different median lacunarities (0.53 vs. 0.59). The aged BC particles showed narrower Feret diameters (229–2557 nm) during navigation than those (78–2926 nm) of freshly emitted BC from the ship's own exhaust during stop. Moreover, tar balls, as one important component of single particles from ship emissions and as the tracer of biomass burning, were identified with geometrical diameters of 160–420 nm in the TEM images. The EDS analyses showed those tar balls are mainly mixed with sea salt, organics, BC, and sulfate. We also found a significant fraction of aged BC in various mixing states (core–shell, embedded) with other components of the aerosol particles after long-range transport. The campaign was further divided into several periods (the before-monsoon period, BMP; transition monsoon period, TMP; after-monsoon period, AMP; and ship pollution period, SPP) according to the wind direction during monsoon and the ship's own pollution. The median absorption Ångström exponent (AAE) values derived from all wavelengths were 1.14, 1.02, 1.08, and 1.06 for BMP, TMP, AMP, and SPP, respectively. Particularly, a median AAE value of 1.93 was obtained during two significant biomass burning events. These results showed that biomass burning (BB) and fossil fuel (FF) combustion contributed to 18 %–22 % and 78 %–82 % of all the BC light absorption without the two intense biomass burning events, during which BB and FF accounted for 42 % and 58 %, respectively. The two BB events originated from the Philippines and Southeast Asia before and after the summer monsoon. Our results demonstrated that BC can serve as the core of aged particles, but the fractal dimensions of BC aggregates were subject to little variation; moreover, such BC particles become much more aggregated after aging in the marine atmosphere, which further affects the light absorption of the BC particles in the SCS.

Effects of biomass burning on CO, HCN, C2H6, C2H2 and H2CO during long-term FTIR measurements in Hefei, China

High-resolution solar absorption spectra were continuously collected by a ground-based Fourier transform infrared (FTIR) spectrometer to retrieve the total column of carbon monoxide (CO), hydrogen cyanide (HCN), ethane (C2H6), acetylene (C2H2), and formaldehyde (H2CO). The time series and variation characteristics of these gases were analyzed. The biomass combustion process is identified by using the correlations between the monthly mean deviations of HCN, C2H6, C2H2 and H2CO versus CO and satellite fire point data. The months with high correlation coefficients (R > 0.8) and peaks of fire point number are considered to be with biomass combustion occurrence. The emissions of HCN, C2H6, C2H2 and H2CO in Anhui were estimated using the enhancement ratios of gases to CO in these months when biomass combustion was the main driving factor of gas concentration change. The study proved the ability of FTIR system in inferring the period during biomass combustion and estimating emissions of the trace gases concerning biomass combustion.

Intercomparison of Air Quality Models in a Megacity: Toward an Operational Ensemble Forecasting System for São Paulo

AbstractAn intercomparison of four regional air quality models is performed in the tropical megacity of São Paulo with the perspective of developing a forecasting system based on a model ensemble. Modeled concentrations of the main regulated pollutants are compared with combined observations in the megacity center, after analyzing the spatial scale of representativeness of air monitoring stations. During three contrasting periods characterized by different types of pollution events, the hourly concentrations of carbon monoxide (CO), nitrogen oxides (NOx), sulfur dioxide (SO2), and particulate matter (PM2.5 and PM10) modeled by the ensemble are in moderate agreement with observations. The median of the ensemble provides the best performance (R ≈ 0.7 for CO, 0.7 for NOx, 0.5 for SO2, 0.5 for PM2.5, and 0.4 for PM10) because each model has periods and pollutants for which it has the best agreement. NOx concentration is modeled with a large inter‐model variability, highlighting potential for improvement of anthropogenic emissions. Pollutants transported by biomass burning events strongly affect the air quality in São Paulo and are associated with significant inter‐model variability. Modeled hourly concentration of ozone (O3) is overestimated during the day (≈20 ppb) and underestimated at night (≈10 ppb), while nitrogen dioxide (NO2) is overestimated at night (≈20 ppb). The observed O3 concentration is best reproduced by the median of the ensemble (R ≈ 0.8), taking advantage of the variable performance of the models. Therefore, an operational air quality forecast system based on a regional model ensemble is promising for São Paulo.

Investigating the Presence of Biomass Burning Events at Ny-Ålesund: Optical and Chemical Insights from Summer-Fall 2019

Summer 2019 is remembered as one of the most intense biomass burning (BB) seasons on record for the Northern Hemisphere. During the MOSAiC expedition, a smoke-dominated layer was identified in the upper troposphere over the North Pole region. The origin of this layer remains unclear, and no evidence has been found to indicate the intrusion of such particles into the Arctic Boundary Layer. The main aim of this work was to evaluate if biomass burning events in the summer 2019 were detectable at Gruvebadet Atmospheric Laboratory, close to Ny-Å lesund (Svalbard Islands) during the second half of 2019. This paper proposes an innovative approach to discriminate biomass burning events based on optical measurements combined with chemical analysis and air mass back-trajectories. Monthly background values of optical coefficients were defined using multi-annual (2018–2021) statistics and twelve possible events were identified. Source apportionment through positive matrix factorization (PMF) identified that the biomass burning factor by PMF accounted for only 2% of the total investigated concentration. The specific biomass burning tracers such as levoglucosan and phenolic compounds were compared with optical measurements and with the PMF results. Air mass trajectory analysis revealed that the early summer fires detected at Ny-Å lesund originated mainly from North America, as also confirmed by the presence of BB factor of PMF, levoglucosan and also vanillic species (softwood combustion tracers). In contrast, the chemical composition and air masses analysis of the highest peak detected in early December suggested residential heating as plausible source, further amplified by the onset of the harsh winter season and the expansion of the polar vortex towards mid-latitudes.