Impact Of Biomass Burning Research Articles

A Nation-by-Nation Assessment of the Contribution of Southeast Asian Open Biomass Burning to PM2.5 in Thailand Using the Community Multiscale Air Quality-Integrated Source Apportionment Method Model

This study utilized the Community Multiscale Air Quality (CMAQ) model to assess the impact of open biomass burning (OBB) in Thailand and neighboring countries—Myanmar, Laos, Cambodia, and Vietnam—on the PM2.5 concentrations in the Bangkok Metropolitan Region (BMR) and Upper Northern Region of Thailand. The Upper Northern Region was further divided into the west, central, and east sub-regions (WUN, CUN, and EUN) based on geographical borders. The CMAQ model was used to simulate the spatiotemporal variations in PM2.5 over a wide domain in Asia in 2019. The Integrated Source Apportionment Method (ISAM) was utilized to quantify the contributions from OBB from each country. The results showed that OBB had a minor impact on PM2.5 in the BMR, but transboundary transport from Myanmar contributed to an increase in PM2.5 levels during the peak burning period from March to April. In contrast, OBB substantially impacted PM2.5 in the Upper Northern Region, with Myanmar being the major contributor in WUN and CUN and domestic burning being the major contributor to EUN during the peak months. Despite Laos having the highest OBB emissions, meteorological conditions caused the spread of PM2.5 eastward rather than into Thailand. These findings highlight the critical impact of regional transboundary transport and emphasize the necessity for collaborative strategies for mitigating PM2.5 pollution across Southeast Asia.

Delayed Impact of Biomass Burning in the Indochinese Peninsula on the Bay of Bengal Monsoon

Delayed Impact of Biomass Burning in the Indochinese Peninsula on the Bay of Bengal Monsoon

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.

Seasonal variation and origins of C1–C5 alkyl nitrates: A year-long study at a Hong Kong coastal site

Alkyl nitrates (RONO₂) are key reactive nitrogen compounds with significant impacts on local and regional air quality. The concentrations of alkyl nitrates can vary significantly across different regions, especially in areas with varying levels of human activity. Long-term observation of alkyl nitrates is necessary to assess the intensity of photochemical reactions and the contributions from different sources. In this study, we present the first continuous year-long monitoring results of eight alkyl nitrates via whole air sample collection and GC-MSD/ECD analysis at a coastal site in Hong Kong. Source apportionment analysis via positive matrix factorization (PMF) revealed distinctive seasonal variations in the source contributions for the eight alkyl nitrate species. Furthermore, increased contributions from biomass combustion were found in autumn and winter, while marine emissions primarily influenced methyl nitrate levels during summer. Our study highlights the significant impact of biomass burning from inland areas on photochemical pollutants in Hong Kong. Cross-regional cooperation in the Greater Bay Area (GBA) is necessary for more comprehensive management of secondary photochemical pollution.

Impacts of Anthropogenic Emissions and Open Biomass Burning in South Asia and Southeast Asia on Air Quality and Meteorology Over Southern China

AbstractThe emissions from South Asia and Southeast Asia significantly impact air quality and meteorological conditions in China. However, the individual or joint contributions of anthropogenic emissions and/or biomass burning from outside China to surface particulate matter with aerodynamic diameters less than 2.5 μm (PM2.5) and aerosol optical depth (AOD) over southern China have not been fully investigated. Here, five experiments were designed to investigate the impacts of these emissions in January (winter), March (pre‐monsoon), and October (post‐monsoon) for 2017. Aerosols from South Asia and Southeast Asia contributed less to southern China during winter and post‐monsoon seasons, whereas the wind patterns and emission intensity during the pre‐monsoon season were conducive to the transport of aerosols. During pre‐monsoon season, the total emissions contributed approximately 5.0 μg m−3 to surface PM2.5 in Xizang Province. Biomass burning in Southeast Asia increased PM2.5 in Yunnan Province by 37.9 μg m−3, while anthropogenic emissions increased it by 8.9 μg m−3. Transboundary aerosols can be transported to Xizang Province and Yunnan Province, primarily influencing PM2.5 below 2 km height. It mainly affected PM2.5 levels above the planetary boundary layer over southeast China. Aerosols from outside China can account for 79.5% and 54.8% AOD in Yunnan Province and southeast China, respectively. These aerosols reduced surface incident solar radiation by approximately 6%, leading to decreases in air temperature, wind speed, and boundary layer height. The findings are only applicable to the pre‐monsoon season.

Source apportionment of particle-bound polycyclic aromatic hydrocarbons (PAHs), oxygenated PAHs (OPAHs), and their associated long-term health risks in a major European city

Many studies have drawn attention to the associations of oxygenated polycyclic aromatic hydrocarbons (OPAHs) with harmful health effects, advocating for their systematic monitoring alongside simple PAHs to better understand the aerosol carcinogenic potential in urban areas. To address this need, this study conducted an extensive PM2.5 sampling campaign in Athens, Greece, at the Thissio Supersite of the National Observatory of Athens, from December 2018 to July 2021, aiming to characterize the levels and variability of polycyclic aromatic compounds (PACs), perform source apportionment, and assess health risk. Cumulative OPAH concentrations (Σ-OPAHs) were in the same range as Σ-PAHs (annual average 4.2 and 5.6 ng m−3, respectively). They exhibited a common seasonal profile with enhanced levels during the heating seasons, primarily attributed to residential wood burning (RWB). The episodic impact of biomass burning was also observed during a peri-urban wildfire event in May 2021, when PAH and OPAH concentrations increased by a factor of three compared to the monthly average. The study period also included the winter 2020–2021 COVID-19 lockdown, during which PAH and OPAH levels decreased by >50 % compared to past winters. Positive matrix factorization (PMF) source apportionment, based on a carbonaceous aerosol speciation dataset, identified PAC sources related to RWB, local traffic (gasoline vehicles) and urban traffic (including diesel emissions), as well as an impact of regional organic aerosol. Despite its seasonal character, RWB accounted for nearly half of Σ-PAH and over two-thirds of Σ-OPAH concentrations. Using the estimated source profiles and contributions, the source-specific carcinogenic potency of the studied PACs was calculated, revealing that almost 50 % was related to RWB. These findings underscore the urgent need to regulate domestic biomass burning at a European level, which can provide concrete benefits for improving urban air quality, towards the new stricter EU standards, and reducing long-term health effects.

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.

Impacts of open biomass burning in Southeast Asia on atmospheric PM2.5 concentrations over south China from 2009 to 2018

Open biomass burning (BB) frequently occurs in spring over Southeast Asia (SEA). The concentration of fine particulate (PM2.5) produced by BB and its impacts on air quality in downwind aeras exhibit significant interannual variations, which are controlled by emission intensity and meteorological circulation. In this study, a regional air quality model system (RAQMS) was applied to investigate the contributions of BB emissions in SEA to atmospheric PM2.5 concentrations over South China in March (a spring month) during 2009–2018 and their interannual variations. Higher near-surface BB-PM2.5 (refers to the PM2.5 produced by BB in SEA) concentrations and contributions were mainly distributed in the source region and its vicinity, while the higher tropospheric BB-PM2.5 concentrations and contributions were characterized by a long belt extending from BB source regions to Yangtze River Delta (YRD) in South China. Combined with the vertical distribution of BB-PM2.5 on the transported path profile, it indicated that higher BB-PM2.5 concentrations were mainly concentrated in 0∼1500 m above the ground over source regions, while the maximum BB-PM2.5 concentrations in the downwind area were distributed in 1500∼3500 m above the ground. The monthly mean tropospheric BB-PM2.5 concentrations were higher in March 2009, 2010, 2012, and 2013, with evident correlation with interannual variation of BB emissions. Sensitivity experiments suggested that the near-surface and tropospheric BB-PM2.5 concentrations over South China had changed by-48.1%∼190.5% and −48.0%∼213.8%, respectively in March 2009–2018 by fixing BB emissions unchanged at the mean of the 10 years, being greater than the changes caused by meteorological conditions and other affecting factors (∼20%). In addition, the relative contributions of BB emission from various regions in SEA on the mean near-surface and tropospheric BB-PM2.5 concentrations over South China were further identified.

Unveiling the Aftermath: Exploring Residue Profiles of Insecticides, Herbicides, and Fungicides in Rice Straw, Soils, and Air Post-Mixed Pesticide-Contaminated Biomass Burning.

This study delved into the impact of open biomass burning on the distribution of pesticide and polycyclic aromatic hydrocarbon (PAH) residues across soil, rice straw, total suspended particulates (TSP), particulate matter with aerodynamic diameter ≤ 10 µm (PM10), and aerosols. A combination of herbicides atrazine (ATZ) and diuron (DIU), fungicide carbendazim (CBD), and insecticide chlorpyriphos (CPF) was applied to biomass before burning. Post-burning, the primary soil pesticide shifted from propyzamide (67.6%) to chlorpyriphos (94.8%). Raw straw biomass retained residues from all pesticide groups, with chlorpyriphos notably dominating (79.7%). Ash residue analysis unveiled significant alterations, with elevated concentrations of chlorpyriphos and terbuthylazine, alongside the emergence of atrazine-desethyl and triadimenol. Pre-burning TSP analysis identified 15 pesticides, with linuron as the primary compound (51.8%). Post-burning, all 21 pesticides were detected, showing significant increases in metobromuron, atrazine-desethyl, and cyanazine concentrations. PM10 composition mirrored TSP but exhibited additional compounds and heightened concentrations, particularly for atrazine, linuron, and cyanazine. Aerosol analysis post-burning indicated a substantial 39.2-fold increase in atrazine concentration, accompanied by the presence of sebuthylazine, formothion, and propyzamide. Carcinogenic PAHs exhibited noteworthy post-burning increases, contributing around 90.1 and 86.9% of all detected PAHs in TSP and PM10, respectively. These insights advance understanding of pesticide dynamics in burning processes, crucial for implementing sustainable agricultural practices and safeguarding environmental and human health.

Significantly Increased Accumulations of PAHs in Scalp Hair During Smoke-haze Period Among Female Adolescents in Chiang Mai, Thailand

Limitations in reporting polycyclic aromatic hydrocarbons (PAHs) accumulated in humans arise from the impact of intense biomass burning and air pollution in upper Southeast Asia. This study analyzed PAHs in human hair samples and explored the associations between ambient PM2.5 and hair PAH concentrations. Follow-up hair collections were conducted on 111 female students, and hair samples with a length of 4 cm were analyzed. Ten different PAHs were identified in the subjects' hair samples. The most substantial pooled estimate of cumulative effects of PM2.5 exposure was observed at lag04 (4-month average). At lag04, every 10 μg/m3 increase in PM2.5 concentration was significantly associated with 0.33, 0.29, 0.35, 0.16, 0.04, 0.64, and 1.66 ng/g hair increases in Acy, Ace, Flu, Ant, Chr, BaP, and total PAHs, respectively (P < 0.05). The findings underscore the significant contribution of ambient PM2.5 exposure to the elevation of PAHs in human hair. Specifically, each centimeter of hair represents a one-month exposure to ambient PM2.5. Moreover, the accumulation of BaP, a carcinogenic PAH, significantly increased at heightened PM2.5 levels, emphasizing the importance of hair analysis in assessing PAH exposure risks and obtaining reliable and comprehensive health risk information. Keywords: Polycyclic aromatic hydrocarbons, Hair analysis, PM2.5

Particulate matter from a tropical city in southeast Brazil: Impact of biomass burning on polycyclic aromatic compounds levels, health risks, and in vitro toxicity

In the context of a rising global temperature, biomass burning represents an increasing risk to human health, due to emissions of highly toxic substances such as polycyclic aromatic hydrocarbon (PAHs). Size-segregated particulate matter (PM) was collected in a region within the sugarcane belt of São Paulo state (Brazil), where biomass burning is still frequent, despite the phasing out of manual harvesting preceded by fire. The median of the total concentration of the 15 PAHs determined was 2.3 ± 1.8 ng m−3 (n = 19), where 63% of this content was in PM1.0. Concentrations of OPAHs and NPAHs were about an order of magnitude lower. PM2.5 collected in the dry season, when most of the fires occur, presented PAHs and OPAHs total concentrations three times higher than in the wet season, showing positive correlations with fire foci number and levoglucosan (a biomass burning marker). These results, added to the fact that biomass burning explained 65% of the data variance (PCA analysis), evidenced the importance of this practice as a source of PAHs and OPAHs to the regional atmosphere. Conversely, NPAHs appeared to be mainly derived from diesel-powered vehicles. The B[a]P equivalent concentration was estimated to be 4 times higher in the dry season than in the wet season, and was greatly increased during a local fire event. Cytotoxicity and genotoxicity of PM1.0 organic extracts were assessed using in vitro tests with human liver HepG2 cells. For both types of tests, significant toxicity was only observed for samples collected during the dry season. Persistent DNA damage that may have impaired the DNA repair system was also observed. The results indicated that there was a health risk associated with the air particulate mixture, mainly related to biomass burning, demonstrating the urgent need for better remediation actions to prevent the occurrence of burning events.

Impacts of Biomass Burning in Southeast Asia on Tropospheric CO2 Concentration Over South China

AbstractThe field observations imply that the long‐range transport of carbon dioxide (CO2) emitted by biomass burning (BB) in Southeast Asia might impact the atmospheric CO2 in South China, while the transboundary path and the contributions of long‐range transport on atmospheric CO2 concentrations in South China remain poorly understood. In this study, a regional air quality model system (RAQMS) was developed by incorporating the atmospheric process of CO2 to investigate the impacts of BB in Southeast Asia on tropospheric CO2 concentration over South China in spring during 2009–2018. CO2 emissions from BB in Southeast Asia in spring varied greatly from 2009 to 2018, and high monthly mean emissions were concentrated in the west of Myanmar, the border between Myanmar, Thailand and Laos, the north of Laos, and Cambodia, with the maximum reaching 1.0 g m−2 hr−1. Higher monthly mean concentrations of near surface CO2 and tropospheric CO2 produced by BB were mainly distributed in the source regions of Southeast Asia and South China. The monthly mean tropospheric CO2 concentrations produced by BB in Southeast Asia were higher in March 2010, 2014, and 2015, which were obviously related to the interannual variation of BB emission, and affected by the atmospheric circulation as well. The contribution of BB emission in Southeast Asia to the net change of tropospheric CO2 concentration in South China presented a belt distribution from the southwest to the northeast, with a domain average of 5.7%–38.6% over South China in March 2009–2018.

The impact of biomass burning occurred in the Indo-China Peninsula on PM2.5 and its spatiotemporal characteristics over Yunnan Province

Being one of the most serious biomass burning regions in the world, the air pollution caused by spring combustion in the Indo-China Peninsula (ICP) has already had an impact on Yunnan Province's beautiful environment and excellent air quality to some extent. In this study, considering the differences in geographical location and topography of Yunnan, we used the K-Means algorithm to divide it into five clustering zones according to the spatiotemporal variation characteristics of PM2.5. Then this study explored the spatial and temporal characteristics of pollution in Yunnan Province and biomass combustion in ICP based on the multi-source data such as MOD14A1, GDAS1, and ground-based PM2.5 data, and used HYSPLIT (Hybrid Single-Particle Lagrangian Integrated Trajectory) pollution tracer analysis and other data statistical methods. The results show that the spatiotemporal variation characteristics of PM2.5 in Yunnan Province show large differences within each clustering zone (CZ). Spatially, CZ 2 has better air quality throughout the year, and the areas with higher PM2.5 are mainly in CZ 1 and CZ 3. Temporally, the months with higher concentration values were mainly from February to April, and also this period owed high biomass burning activities in the ICP, which resulted in pollution values exceeding 60 μg/m3 within certain CZs. Finally, the results of the pollution tracer analysis showed that within CZs other than CZ 2, the contribution due to the burning in the ICP was variable, and that the countries with a high contribution of pollution to Yunnan Province were Myanmar, and the other sources of pollution are mainly caused by local and neighbouring anthropogenic activities. Therefore, based on overall improvement of air quality, Yunnan Province is necessary to prevent and control not only the pollutants from the ICP from February to April, but also the pollution caused by the emissions from rapid economic development.

Synergic use of in-situ and remote sensing techniques for comprehensive characterization of aerosol optical and microphysical properties

We report on importance of conducting comprehensive studies of atmospheric aerosol particles, which cannot be done if information from various complementary sensors is unavailable. We present an example for such application and recommend on the types of sensors that should be used in view of the ACTRIS and RI-URBANS new strategies for monitoring at supersites. Although active and passive remote sensing data was not available in continuous mode, we show that synergic use of them with in-situ observations allows for comprehensive study of temporal and height-resolved distribution of aerosol in the lower troposphere and it can be successfully combined to assess biomass burning impact on air quality and optical properties.The analysed period was divided into three episodes based on the measured black carbon (BC) concentration and the prevailing wind direction. The dominant 72-h backward trajectories were ending in western Europe, mid-Atlantic and western Russia, respectively, The in-situ measured mass concentrations of BCtotal and BC apportioned to biomass burning as well as particulate matter (PM) concentrations in accumulation mode were twice higher during the first and last episodes compared to the second episode, representing long-range transport from different source regions. The obtained complementary surface, column-integrated, and layer-derived size distributions and other parameters demonstrate the added value of multisensor analyses.

Characteristics and health risk assessment of indoor and outdoor PM2.5 in a rural village, in Northeast of China: impact of coal and biomass burning.

Fine particulate matter (PM2.5) has health effects that may depend on its sources and chemical composition. In this study, characteristics of PM2.5 chemical composition and health risk assessment from Songyuan, China, were investigated during day and night in indoor and outdoor from February 4 to 19, 2021. Relative high concentrations of PM2.5 were obtained in indoor environment than outdoor, with 503.95 ± 209.62μg/m3 during the day and 357.52 ± 232.81μg/m3 at night for the indoor environment. Relatively high total carbon, organic carbons, elemental carbons, polycyclic aromatic hydrocarbons (PAHs), and oxygenated polycyclic aromatic hydrocarbons (OPAHs) were obtained in indoor environment. However, the average concentrations of PAHs were higher during night (73.57 ± 43.09ng/m3) in indoor and OPAHs during day (6.027 ± 2.960ng/m3) in outdoor. They had different I/O distributions of these compounds during day and night. Indeno(1,2,3-cd) pyrene was the dominant PAHs, and benzanthrone was the dominant OPAHs; this is different with the previous studies. The high indoor/outdoor ratios showed the indoor coal and biomass burning greatly affect the indoor pollutants. Average ILCR health risk assessment for PAHs was all higher than 10-6 for different age gender, suggesting there has potential cancer risk existed for populations living in the rural coal and biomass burning area Songyuan, China.

New particle formation in the tropical free troposphere during CAMP2Ex: statistics and impact of emission sources, convective activity, and synoptic conditions

Abstract. Nucleation in the free troposphere (FT) and subsequent growth of new particles represent a globally important source of cloud condensation nuclei (CCN). Whereas new particle formation (NPF) has been shown to occur frequently in the upper troposphere over tropical oceans, there have been few studies of NPF at lower altitudes. In addition, the impact of urban emissions and biomass burning on the NPF in tropical marine FT remains poorly understood. In this study, we examine NPF in the lower and mid-troposphere (3–8.5 km) over the tropical ocean and coastal region using airborne measurements during the recent Cloud, Aerosol and Monsoon Processes Philippines Experiment (CAMP2Ex). NPF was mostly observed above 5.5 km and coincided with elevated relative humidity (RH) and reduced condensation sink (CS), suggesting that NPF occurs in convective cloud outflow. The frequency of NPF increases with altitude, reaching ∼ 50 % above 8 km. An abrupt decrease in NPF frequency coincides with early monsoon transition and is attributed to increased CS resulting from reduced convective activity and more frequent transport of aged urban plumes. Surprisingly, a large fraction of NPF events in background air were observed in the early morning, and the NPF is likely made possible by very low CS despite low actinic flux. Convectively detrained biomass-burning plumes and fresh urban emissions enhance NPF as a result of elevated precursor concentrations and scavenging of pre-existing particles. In contrast, NPF is suppressed in aged urban plumes where the reactive precursors are mostly consumed, while CS remains relatively high. This study shows a strong impact of urban and biomass-burning emissions on the NPF in tropical marine FT. The results also illustrate the competing influences of different variables and interactions among anthropogenic emissions, convective clouds, and meteorology, which lead to NPF under a variety of conditions in tropical marine environments.

Fuel-Type Independent Parameterization of Volatile Organic Compound Emissions from Western US Wildfires.

Volatile organic compounds (VOCs) emitted from biomass burning impact air quality and climate. Laboratory studies have shown that the variability in VOC speciation is largely driven by changes in combustion conditions and is only modestly impacted by fuel type. Here, we report that emissions of VOCs measured in ambient smoke emitted from western US wildfires can be parameterized by high- and low-temperature pyrolysis VOC profiles and are consistent with previous observations from laboratory simulated fires. This is demonstrated using positive matrix factorization (PMF) constrained by high- and low-temperature factors using VOC measurements obtained with a proton-transfer reaction time-of-flight mass spectrometer (PTR-ToF-MS) on board the NASA DC-8 during the FIREX-AQ (Fire Influence on Regional and Global Environments and Air Quality) project in 2019. A linear combination of high- and low-temperature factors described more than 70% of the variability of VOC emissions of long-lived VOCs in all sampled wildfire plumes. An additional factor attributable to atmospheric aging was required to parameterize short-lived and secondarily produced VOCs. The relative contribution of the PMF-derived high-temperature factor for a given fire plume was strongly correlated with the fire radiative power (FRP) at the estimated time of emission detected by satellite measurements. By combining the FRP with the fraction of the high-temperature PMF factor, the emission ratios (ERs) of VOCs to carbon monoxide (CO) in fresh wildfires were estimated and agree well with measured ERs (r2 = 0.80-0.93).

Chemical processes of wintertime aerosols over the East China Sea based on aircraft and ground measurements: Comparison with the Sea of Japan

Aircraft and ground-level observations of wintertime aerosols over the East China Sea (ECS) around Japan's southwestern islands were conducted from the boundary layer to the middle troposphere (0–4.5 km) and compared to those over the Sea of Japan (SOJ) during the same period, for the purpose of comprehensive elucidation on modification process of chemical composition in aerosols at the Asian outflow receptor regions. The deficient values of Cl− in both cases for ECS and SOJ were higher at ground level than at high altitudes because of the acidic gas (HNO3, H2SO4) concentrations. Most Na+ and Cl− at high altitudes and at ground level originated from sea salt, because the (Na+ + Cl−) concentrations of which in the boundary layer observed were linearly related to the production flux of sea spray aerosol. The contribution of sea salt aerosols to cloud condensation nuclei appears to be low over the ECS, contrary to the SOJ. The non-sea salt (nss)-K+ concentrations and the path of backward trajectories suggest a significant impact of biomass burning on the SOJ associated with woodburning for residential heating in the Korean Peninsula. A similar difference was observed in NH4+/nss-SO42– equivalent ratios (∼0.5 for the ECS; ∼1 for the SOJ), which likely indicates ammonium sulfate aerosols produced in urban and industrial regions of Korea. The high aerosol Ca2+ concentration in the boundary layer over the ECS was accompanied by those of Na+, Cl−, NO3−, and nss-SO42– during cold front passages, as observed in SOJ. This indicates that Ca(NO3)2, CaSO4, and CaCl2 were formed via the reactions of acidic gases and Ca-rich dust particles from desert areas in the Asian continent, followed by the production of NaNO3 by uptake of acidic gases into sea salt in the ECS. This notion is supported by high Se(VI)/Se (IV) ratios (>2) that indicate an oxidative process during long-range transport from coal combustion sources.

Impacts of Biomass Burning in Southeast Asia on Tropospheric CO2 Concentration over South China

Impacts of Biomass Burning in Southeast Asia on Tropospheric CO2 Concentration over South China

Constraining emissions of volatile organic compounds from western US wildfires with WE-CAN and FIREX-AQ airborne observations

Abstract. The impact of biomass burning (BB) on the atmospheric burden of volatile organic compounds (VOCs) is highly uncertain. Here we apply the GEOS-Chem chemical transport model (CTM) to constrain BB emissions in the western USA at ∼ 25 km resolution. Across three BB emission inventories widely used in CTMs, the inventory–inventory comparison suggests that the totals of 14 modeled BB VOC emissions in the western USA agree with each other within 30 %–40 %. However, emissions for individual VOCs can differ by a factor of 1–5, driven by the regionally averaged emission ratios (ERs, reflecting both assigned ERs for specific biome and vegetation classifications) across the three inventories. We further evaluate GEOS-Chem simulations with aircraft observations made during WE-CAN (Western Wildfire Experiment for Cloud Chemistry, Aerosol Absorption and Nitrogen) and FIREX-AQ (Fire Influence on Regional to Global Environments and Air Quality) field campaigns. Despite being driven by different global BB inventories or applying various injection height assumptions, the model–observation comparison suggests that GEOS-Chem simulations underpredict observed vertical profiles by a factor of 3–7. The model shows small to no bias for most species in low-/no-smoke conditions. We thus attribute the negative model biases mostly to underestimated BB emissions in these inventories. Tripling BB emissions in the model reproduces observed vertical profiles for primary compounds, i.e., CO, propane, benzene, and toluene. However, it shows no to less significant improvements for oxygenated VOCs, particularly for formaldehyde, formic acid, acetic acid, and lumped ≥ C3 aldehydes, suggesting the model is missing secondary sources of these compounds in BB-impacted environments. The underestimation of primary BB emissions in inventories is likely attributable to underpredicted amounts of effective dry matter burned, rather than errors in fire detection, injection height, or ERs, as constrained by aircraft and ground measurements. We cannot rule out potential sub-grid uncertainties (i.e., not being able to fully resolve fire plumes) in the nested GEOS-Chem which could explain the negative model bias partially, though back-of-the-envelope calculation and evaluation using longer-term ground measurements help support the argument of the dry matter burned underestimation. The total ERs of the 14 BB VOCs implemented in GEOS-Chem only account for half of the total 161 measured VOCs (∼ 75 versus 150 ppb ppm−1). This reveals a significant amount of missing reactive organic carbon in widely used BB emission inventories. Considering both uncertainties in effective dry matter burned (× 3) and unmodeled VOCs (× 2), we infer that BB contributed to 10 % in 2019 and 45 % in 2018 (240 and 2040 Gg C) of the total VOC primary emission flux in the western USA during these two fire seasons, compared to only 1 %–10 % in the standard GEOS-Chem.