Average Elemental Carbon Concentrations Research Articles

Sources and composition of elemental carbon during haze events in North China by a high time-resolved study

Despite the implementation of stringent emission reduction measures in the past year, severe winter haze events still occurred frequently in North China, with only marginal decreases observed in elemental carbon (EC) concentrations. EC not only constitutes a fraction of particle mass but also interacts with boundary layer and influences haze formation. Given the complex composition of EC, characterizing its sources and composition during haze processes is challenging yet crucial for understanding haze formation and evolution. Here, hourly-resolution PM2.5 samples were collected during three different haze event (P1-P3) in the North China Plain to investigate dynamic changes in EC source across different haze processes. The average EC concentrations and char/soot ratios were 9.94 ± 4.80 μgC·m−3, 14.5 ± 6.93 μgC·m−3, 15.9 ± 5.54 μgC·m−3, and 2.42 ± 0.98, 2.70 ± 0.88, 2.61 ± 0.95 for P1, P2 and P3, respectively. Backward trajectory analysis showed distinct variations in EC concentration and composition under the influence of different air masses during the three haze events, with local air masses influenced days exhibiting higher EC concentrations and char/soot ratios. The char/soot ratio based diagnostic method suggested that EC was predominantly influenced by coal combustion and vehicle emissions. Further positive matrix factorization analysis suggested that biomass burning and residential coal combustion were the main contributors of EC (58 %) and played a dominant role in driving variations in EC concentrations during haze episodes. Potential source contribution function analysis results highlight that local biomass burning and residential coal combustion could be major reason for the EC elevation in different haze events. Our results provide valuable insights into the sources and composition of EC during haze events, facilitating the implementation of effective measures for mitigating both EC and PM pollution.

Long-term characterization of organic and elemental carbon at three different background areas in northern Europe

Elemental carbon (EC) and organic carbon (OC) are major components of atmospheric PM2.5. In this article we represent the results of long-term measurements (8–12 years) of EC and OC at three different background sites in Finland: in a rural area (Virolahti) since the summer 2010, in a marine environment (Utö) since the summer 2011, and in a clean arctic environment (Pallas/Matorova) since 2014. The concentrations of OC and EC were measured with a semi-continuous organic and elemental carbon analyser (SC-OCEC) in all the sites. The yearly average concentrations of OC varied between 0.96–3.1, 0.76–1.6 and 0.30–0.69 μg m−3 at the rural (Virolahti), marine (Utö) and arctic (Pallas/Matorova) sites, respectively. Similarly, the corresponding yearly average concentrations of EC ranged between 0.095–0.48, 0.090–0.2 and 0.010–0.086 μg m−3 at those sites. A clear seasonal variation in OC and EC concentrations was observed at each measurement site. OC concentrations were highest during summertime whereas EC concentrations were highest in wintertime. The seasonality of OC was clearest at the Arctic site that had also the largest temperature variation and shortest growing season resulting in a sharp increase in OC concentrations from June to August. At all the measurement sites, OC concentrations gradually increased when the temperature rose over sub-zero temperatures whereas the daily average EC concentrations did not show as apparent temperature dependence as OC. Based on the cluster analysis, highest OC and EC concentrations, and the highest total load for EC (23–32%), at all the sites were detected with the air mass origin of southeast. In the marine environment, the effect of black carbon from ship plumes was investigated. The limit for ship fuel sulfur content changed during the measurement period (in January 2015), but it was not observed to influence the Optical EC concentrations. Overall, long-term, continuous measurements are crucial when the time trends in air quality and the effect of emission mitigation actions are investigated. In this study, a slight decrease in OC was observed at the Marine site, however, a decrease for EC was seen both at the rural and marine sites suggesting that the emission mitigation actions like EURO limits for light vehicles or improved after-treatment systems developed for industry and energy production have already decreased the background concentrations in rural areas.

Secondary formation and source analysis of carbonaceous components in PM1 in a typical city, Southwest of China

Carbonaceous components are major components of PM1, which have a significant impact on climate change, air quality and human health. However, the secondary formation and source analysis of carbonaceous components in PM1 are still unclear. Therefore, in order to study the secondary formation and sources of carbonaceous components in PM1, PM1 samples were collected in Chengdu, a typical city located in southwest of China, from 2018 to 2019. The concentrations of organic carbon (OC), elemental carbon (EC) and isotopic compositions of carbon (δ13C) in PM1 were determined using a thermal/optical carbon analyzer and elemental analyzer-isotope ratio mass spectrometer. In addition, the δ13C values from relevant potential sources (C3 plants, C4 plants, vehicle exhaust and coal) were also determined. The results showed that the annual average concentrations of OC and EC in PM1 in Chengdu were 6.43 ± 3.30 μg·m−3 and 1.99 ± 0.98 μg·m−3, accounting for 13.83% and 4.28% of the PM1 mass concentration, respectively. The concentrations of OC in PM1 ranked in the order of winter > summer > spring > autumn, while the concentrations of EC varied in the order of winter > spring > autumn > summer. The concentrations of OC and EC in PM1 reached the maximum in winter, mainly due to the special meteorological conditions and significantly higher pollutant emissions. The correlations of OC and EC were higher in spring, autumn and winter, and lower in summer. It showed that OC and EC might have the same sources in spring, autumn and winter, while the sources of OC and EC were relatively complex in summer. The annual average concentration of secondary organic carbon (SOC) in PM1 was 2.23 ± 1.22 μg·m−3. The concentrations of SOC were higher in autumn and winter and lower in spring and summer. The special meteorological conditions and significantly higher pollutant emissions are important reasons for the higher SOC concentrations in winter. On the other hand, the low temperature in winter can also promote the formation of SOC. The results of carbon isotopic compositions indicated that the carbonaceous components in PM1 were mainly derived from vehicle exhaust (52.4%), C3 plants combustion (26.2%), coal burning (16.2%) and C4 plants combustion (5.2%). The findings help to deepen the understanding of the secondary formation and sources of carbonaceous components in PM1 and provide theoretical guidance for environmental management.

Chemical characterization of marine aerosols from two cruises over the South China Sea: Importance of biomass burning and secondary formation

Total suspended particle (TSP) samples were collected during June–July 2015 in the northern South China Sea (NSCS) and August–September 2016 in the western South China Sea (WSCS). Water-soluble ions (WSIs), organic carbon (OC), elemental carbon (EC), and organic compounds were measured. The average concentrations of WSIs, OC, EC and organic compounds were 19.4 ± 10.9 μg m−3, 2.48 ± 1.54 μgC m−3, 0.31 ± 0.25 μgC m−3 and 789 ± 217 ng m−3 in the NSCS, and were 10.2 ± 4.71 μg m−3, 1.76 ± 1.82 μgC m−3, 0.43 ± 0.32 μgC m−3 and 781 ± 342 ng m−3 in the WSCS. In both cruises, sea salt ions (Na+ and Cl−) and secondary inorganic ions (SO42−, NO3−, and NH4+) were the main species of WSIs, accounting for 54.0 % and 43.6 % in the NSCS, and for 35.0 % and 54.0 % in the WSCS. The secondary products (dicarboxylic acids and aromatic acids) (NSCS: 73.3 %; WSCS: 73.9 %) and saccharides (NSCS: 19.0 %; WSCS: 18.0 %) accounted large fractions of organic compounds in aerosol particles over the SCS. These results suggest sea salt emissions and secondary formation are the main sources of the aerosols over the SCS in summer. The positive correlations between the biomass burning tracers (nss-K+ and levoglucosan) and OC as well as organic compounds indicated that biomass burning from nearby continents was also an important source of organic aerosols over the SCS. Based on back-trajectory analysis and satellite fire spots, Indochina Peninsula and China were proposed as the main continental source areas of non-sea salt WSIs and organic compounds. Our results highlight the significant contribution of continental outflow especially biomass burning and photochemical secondary oxidation to the organic compositions of aerosol particles over the SCS in summertime.

Distribution Characteristics and Source Apportionment of Winter Carbonaceous Aerosols in a Rural Area in Shandong, China

PM2.5 samples were collected for 15 consecutive days in a rural area in Shandong from January to February 2022. The carbon components and water-soluble ions in PM2.5 were measured, and the distribution characteristics and sources of the carbonaceous aerosols were analysed. It was found that the concentrations of PM2.5 in the region were high in winter (55.79–236.11 μg/m³). Organic carbon (OC) and elemental carbon (EC) accounted for 11.61% and 4.57% of PM2.5, respectively. The average concentrations of OC (19.01 μg/m³) and EC (7.49 μg/m³) in PM2.5 were high. The mean value of secondary organic carbon (SOC), estimated by the minimum R squared (MRS) method, was 14.76 μg/m3, accounting for a high proportion of OC (79.41%). Four OC fractions (OC1, OC2, OC3, and OC4) were significantly correlated with SOC, indicating that the OC components contained a large amount of SOC. OC3, OC4, EC1, and OC2 dominated (accounting for 80% of TC) among the eight carbon fractions. Water-soluble organic carbon (WSOC, 12.82 μg/m³) and methanol-soluble organic carbon (MSOC) (16.28 μg/m³) accounted for 67.47% and 84.99% of OC, respectively, indicating that SOC accounted for a high proportion of OC. The proportion of eight water-soluble ions in PM2.5 was 47.48%. NH4+ can neutralise most of the SO42− and NO3−, forming (NH4)2SO4 and NH4NO3, while Cl− mainly exists in the form of KCl and MgCl2. The ratios of some typical components showed that PM2.5 was not only affected by local combustion sources, but also by mobile sources. The cluster analysis results of the backward trajectory model showed that primary and secondary sources in Shandong Province had a great impact on PM2.5 (64%). The analysis results of the positive matrix factorisation (PMF) model showed that the sources of PM2.5 in the region included mobile sources, primary combustion sources, secondary sources, and dust sources, among which secondary sources contributed the most (60.46%).

Seasonal variations of mass absorption efficiency of elemental carbon in PM2.5 in urban Guangzhou of South China

This study investigates seasonal variations of mass absorption efficiency of elemental carbon (MAEEC) and possible influencing factors in urban Guangzhou of South China. Mass concentrations of elemental carbon (EC) and organic carbon (OC) in PM2.5 and aerosol absorption coefficient (bap) at multi-wavelengths were simultaneously measured in four seasons of 2018–2019 at hourly resolution by a semi-continuous carbon analyzer and an aethalometer. Seasonal average mass concentrations of EC were in the range of 1.36–1.70 µgC/m3 with a lower value in summer than in the other seasons, while those of OC were in the range of 4.70–6.49 µgC/m3 with the lowest value in summer and the highest in autumn. Vehicle exhaust from local traffic was identified to be the predominant source of carbonaceous aerosols. The average aerosol absorption Ångström exponents (AAE) were lower than 1.2 in four seasons, indicating EC and bap were closely related with vehicle exhaust. Seasonal MAEEC at 550 nm was 11.0, 8.5, 10.4 and 11.3 m2/g in spring, summer, autumn, and winter, respectively. High MAEEC was related with the high mass ratio of non-carbonaceous aerosols to EC and high ambient relative humidity.

Chemical characterizations and sources of PM2.5 over the offshore Eastern China sea: Water soluble ions, stable isotopic compositions, and metal elements

Marine aerosols are mainly sea salt or secondary-formation non-sea salt (nss) inorganic ions and organic compounds released from the ocean, which are modified by substances from terrestrial sources via long-distance transport. Atmospheric particulate matter (PM2.5) was collected during a ship campaign over the offshore eastern China Sea (OECS) from April 20, 2018 to May 18, 2018. Nine water-soluble ions (WSIs), organic carbon (OC), elemental carbon (EC), stable carbon/nitrogen isotopes, and twenty-six metal elements were analyzed. The average concentrations of WSIs, OC, and EC were 13.73 ± 4.89, 2.55 ± 1.95, and 0.72 ± 0.56 μg/m3, respectively. SO42−, NH4+, and NO3− were the predominant species among the WSIs, accounting for 53.2, 16.1, and 11.6% of the total ion mass, respectively. A strong correlation between OC and EC (r2 = 0.79) was found, indicating that they may be derived from common sources. The δ13CTC values ranged from −26.44 to −23.63‰, with an average of −25.82 ± 0.67‰, while δ15NTN values were in the range of −2.19 and 6.97‰, with an average of 5.40 ± 2.05‰. The overlapping isotopic ratios combined with the correlation results suggested that emissions from coal-fired activities and biomass burning were major factors affecting marine aerosols in the OECS. Twenty-six metal elements were classified into natural, anthropogenic, or mixed sources based on their enrichment factors, and more than 60% of the elements were affected by anthropogenic sources. Positive matrix factorization (PMF) analysis identified five potential source factors of PM2.5, including marine sources, vehicular exhaust, crustal sources, secondary formation, and combustion sources, while anthropogenic sources (vehicular exhaust, secondary formation, and combustion sources) accounted for 78.0% of all sources.

Significant reduction in atmospheric organic and elemental carbon in PM2.5 in 2+26 cities in northern China

To better understand the change characteristics and reduction in organic carbon (OC) and elemental carbon (EC) in particulate matter (PM) with a diameter of ≤2.5 μm (PM2.5) driven by the most stringent clean air policies and pandemic-related lockdown measures in China, a comprehensive field campaign was performed to measure the carbonaceous components in PM2.5 on an hourly basis via harmonized analytical methods in the Beijing-Tianjin-Hebei and its surrounding region (including 2 + 26 cities) from January 1 to December 31, 2020. The results indicated that the annual average concentrations of OC and EC reached as low as 6.6 ± 5.7 and 1.8 ± 1.9 μg/m3, respectively, lower than those obtained in previous studies, which could be attributed to the effectiveness of the Clean Air Action Plan and the impact of the COVID-19-related lockdown measures implemented in China. Marked seasonal and diurnal variations in OC and EC were observed in the 2 + 26 cities. Significant correlations (p < 0.001) between OC and EC were found. The annual average secondary OC levels level ranged from 1.8–5.4 μg/m3, accounting for 37.7–73.0% of the OC concentration in the 2 + 26 cities estimated with the minimum R squared method. Based on Interagency Monitoring of Protected Visual Environments (IMPROVE) algorithms, the light extinction contribution of carbonaceous PM to the total amount reached 21.1% and 26.0% on average, suggesting that carbonaceous PM played a less important role in visibility impairment than did the other chemical components in PM2.5. This study is expected to provide an important real-time dataset and in-depth analysis of the significant reduction in OC and EC in PM2.5 driven by both the Clean Air Action Plan and COVID-19-related lockdown policies over the past few years, which could represent an insightful comparative case study for other developing countries/regions facing similar carbonaceous PM pollution.

A Study of Socio-Economic Impact of Soft Approaches of Climate Adaptation using Changing Fuel Practice in Indoor Air at Rural Sites in India

Majority of India’s rural population depends on biomass burning for cooking and heating purposes on traditional cook stoves called Chullah which results into indoor air pollution. The sampling for this study was carried out in two villages of India viz. Budhwada, Madhya Pradesh (M.P.) and Baggi, Himachal Pradesh (H.P.). Both the regions are significantly different in terms of culture, traditions, topography and daily practices and hence this study helped in understanding the contrast between these regions. The concentrations of carbonaceous aerosols viz. OC (Organic Carbon) and EC (Elemental Carbon) were evaluated for different fuel use in four different houses of each village. Introducing the concept of soft approaches, the residents were asked to bring certain changes in their practices by cooking either with solid biomass or Liquefied Petroleum Gas (LPG) as fuel. The overall average concentration of OC was found to be higher for Budhwada (M.P.) at 124.34 ± 34.68 µg/m3 than at Baggi, (H.P.) with value 105.26 ± 35.63 µg/m3 whereas the reverse was true for the average concentration of EC with value 62.98 ± 20.75 µg/m3 at Baggi, (H.P.) and 55.51 ± 15.51 µg/m3 at Budhwada (M.P.). The average OC and EC concentrations from solid biomass fuel (dung cake) burning at Budhwada (M.P.) was respectively higher by 56.14% and 33.57% as compared to the LPG usage. Similarly, in Baggi (H.P.) village with LPG usage, a significant reduction was observed in OC and EC concentrations (76.69% and 70.10% respectively) when compared with fuelwood burning. House-wise and time-wise variations of carbonaceous aerosols at both the sites confirmed that their concentrations are lower in houses with greater ventilation and higher in cooking times (morning and evening). In Budhwada (M.P.), the concentrations of K+, Ca2+ and SO42- ions decreased significantly from dung cake to LPG use by 67.91%, 76.98% and 51.85% respectively. In Baggi (H.P.), K+ ion concentration was decreased by 63.4% from fuelwood to LPG use. A questionnaire survey conducted on the residents also corroborated the above findings where the residents agreed that LPG use has health benefits over solid biomass fuel usage but the challenges such as supply of LPG into rural interiors, financial feasibility, etc. were of serious concern. Also, changing the contemporary mindset of rural population is a challenging task.

Water-insoluble carbonaceous components in rainwater over an urban background location in Northern India during pre-monsoon and monsoon seasons.

The carbonaceous content of rainwater was investigated in samples collected at an urban background site in northern India. Sampling was performed on an event basis during two seasons: pre-monsoon (PM) and monsoon (MN) season covering May-June and July-August, respectively, in 2016. The concentrations of different fractions of water-insoluble organic carbon (WIOC) and elemental carbon (EC) were precisely determined, and the sources of WIOC and EC were also analysed. The result revealed that the average WIOC and EC concentration in rainwater ranged from 0.4 to 52 mgC/L and from 0.1 to 15.3 mgC/L, respectively. The concentrations of WIOC and EC were found to be ~ 9 times and ~ 12 times higher, respectively, in the PM season than MN season. The WIOC/EC ratio indicated higher variation in PM season as compared to that of the MN season, suggesting divergent emission sources during the PM season. The formation of water-insoluble secondary organic carbon (WISOC) has also been identified as one of the causes for the extensive difference in the WIOC/EC ratio in different seasons. Results showed that the WIOC and its fractions were efficiently scavenged through rain. While EC and its fractions were less significantly scavenged, due to its hydrophobicity and fine size. The atmospheric scavenging coefficients of selected carbonaceous components were found significantly correlated with rain intensity (RI) during both the seasons. Higher rain intensity caused greater rates of carbonaceous component wash-out and decreasing concentrations of carbonaceous components in the rain.

Ambient Levels, Emission Sources and Health Effect of PM2.5-Bound Carbonaceous Particles and Polycyclic Aromatic Hydrocarbons in the City of Kuala Lumpur, Malaysia

With increasing interest in understanding the contribution of secondary organic aerosol (SOA) to particulate air pollution in urban areas, an exploratory study was carried out to determine levels of carbonaceous aerosols and polycyclic aromatic hydrocarbons (PAHs) in the city of Kuala Lumpur, Malaysia. PM2.5 samples were collected using a high-volume sampler for 24 h in several areas in Kuala Lumpur during the north-easterly monsoon from January to March 2019. Samples were analyzed for water-soluble organic carbon (WSOC), organic carbon (OC), and elemental carbon (EC). Secondary organic carbon (SOC) in PM2.5 was estimated. Particle-bound PAHs were analyzed using gas chromatography-flame ionization detector (GC-FID). Average concentrations of WSOC, OC, and EC were 2.73 ± 2.17 (range of 0.63–9.12) µg/m3, 6.88 ± 4.94 (3.12–24.1) µg/m3, and 3.68 ± 1.58 (1.33–6.82) µg/m3, respectively, with estimated average SOC of 2.33 µg/m3, contributing 34% to total OC. The dominance of char-EC over soot-EC suggests that PM2.5 is influenced by biomass and coal combustion sources. The average of total PAHs was 1.74 ± 2.68 ng/m3. Source identification methods revealed natural gas and biomass burning, and urban traffic combustion as dominant sources of PAHs in Kuala Lumpur. A deterministic health risk assessment of PAHs was conducted for several age groups, including infant, toddler, children, adolescent, and adult. Carcinogenic and non-carcinogenic risk of PAH species were well below the acceptable levels recommended by the USEPA. Backward trajectory analysis revealed north-east air mass brought pollutants to the studied areas, suggesting the north-easterly monsoon as a major contributor to increased air pollution in Kuala Lumpur. Further work is needed using long-term monitoring data to understand the origin of PAHs contributing to SOA formation and to apply source-risk apportionment to better elucidate the potential risk factors posed by the various sources in urban areas in Kuala Lumpur.

Seasonal Trends of Organic and Elemental Carbon in PM1 Measured over an Industrial Area of Delhi, India

The present study was carried out to investigate the seasonal variation of organic carbon (OC) and elemental carbon (EC) in PM1 during 2018–2019 in the industrial area of Delhi, India. A cascade impactor was used to collect aerosol particles in four different size fractions (≥ PM10, PM2.5–10, PM2.5–1, ≤ PM1). The OC/EC analysis was performed by thermal/optical carbon analyzer (DRI 2001). The highest concentration of aerosol particles was observed in PM1 among four different size fractions (≥ PM10: 37.77 ± 16.07 µg/m3, PM2.5–10: 90.28 ± 41.84 µg/m3, PM2.5–1: 81.65 ± 43.85 µg/m3, and ≤ PM1: 151.75 ± 58.57 µg/m3). The annual average concentration of OC and EC in PM1 was found to be 34.12 ± 22.94 µg/m3 and 13.91 ± 11.45 µg/m3, respectively. Furthermore, a clear seasonal difference in the concentrations of OC and EC was observed. The highest OC and EC concentration were found during post-monsoon (OC: 59.58 ± 21.66 µg/m3) and winter season (EC: 23.90 ± 12.08 µg/m3), respectively. Although the lowest concentration of OC and EC was observed in the monsoon season (OC: 12.08 ± 6.98 µg/m3, EC: 3.88 ± 1.97 µg/m3). The annual average percentage contribution of OC and EC in PM1 was observed to be 22.48 and 9.16%, respectively. Total carbonaceous aerosol (TCA) accounted for 45.18% of PM1. The annual average OC/EC ratio was found to be 2.45, which indicates the secondary organic aerosol (SOA) formation. The OC/EC analysis reveals that OC2 and EC1 were dominant among eight carbon subfractions, which suggest a mixed source of emission. The higher value of inhalation dose of EC was observed during the winter season (309 µg), which can lead to a higher risk of cardiac and respiratory illness.

Carbonaceous Aerosols in PM1, PM2.5, and PM10 Size Fractions over the Lanzhou City, Northwest China

Carbonaceous particles have been confirmed as major components of ambient aerosols in urban environments and are related to climate impacts and environmental and health effects. In this study, we collected different-size particulate matter (PM) samples (PM1, PM2.5, and PM10) at an urban site in Lanzhou, northwest China, during three discontinuous one-month periods (January, April, and July) of 2019. We measured the concentrations and potential transport pathways of carbonaceous aerosols in PM1, PM2.5, and PM10 size fractions. The average concentrations of OC (organic carbon) and EC (elemental carbon) in PM1, PM2.5, and PM10 were 6.98 ± 3.71 and 2.11 ± 1.34 μg/m3, 8.6 ± 5.09 and 2.55 ± 1.44 μg/m3, and 11.6 ± 5.72 and 4.01 ± 1.72 μg/m3. The OC and EC concentrations in PM1, PM2.5, and PM10 had similar seasonal trends, with higher values in winter due to the favorable meteorology for accumulating pollutants and urban-increased emissions from heating. Precipitation played a key role in scavenge pollutants, resulting in lower OC and EC concentrations in summer. The OC/EC ratios and principal component analysis (PCA) showed that the dominant pollution sources of carbon components in the PMs in Lanzhou were biomass burning, coal combustion, and diesel and gasoline vehicle emissions; and the backward trajectory and concentration weight trajectory (CWT) analysis further suggested that the primary pollution source of EC in Lanzhou was local fossil fuel combustion.

Seasonal Variation of Carbonaceous Species of PM2.5 in a Small City in Sichuan Basin, China

Organic carbon (OC) and elemental carbon (EC) concentrations were measured in daily PM2.5 samples collected over four non-consecutive months representing four seasons from 2016 to 2017 in a small city in the east of Sichuan Basin. The average concentrations of OC and EC during the study periods were observed to be 15.5 ± 13.5 and 5.2 ± 4.7 μg∙m−3, respectively, both with the highest in winter. The OC and EC correlated well in fall and winter, implying that OC and EC were attributed to common emission sources. The estimated secondary OC (SOC) represented 37.2%, 46.7%, 26.9%, and 40.7% of the OC in spring, summer, fall, and winter, respectively. The highest concentration of SOC was found in winter, while the proportion of SOC/OC was highest in summer. Strong correlations were observed between OC vs. K+ and EC vs. K+ in fall and winter, suggesting that biomass burning was a significant source of carbonaceous aerosols. Four sources of OC and EC were resolved by the positive matrix factorization (PMF) model, including coal combustion (5.5% and 12.1%), building and road dust (19.7% and 18.1%), biomass burning (38.7% and 33.1%), and vehicle emission (36.1% and 36.7%), respectively. The potential source contribution function (PSCF) analysis signified that the main source areas of OC and EC were distributed in or nearby Wanzhou.

Seasonal variation of carbonaceous species in PM1 measured over residential area of Delhi, India

Seasonal variation in the concentration of Organic Carbon (OC) and Elemental Carbon (EC) was investigated in PM1 size fraction over a residential area in Delhi, India. The sampling was carried out using a cascade impactor from April 2018 to March 2019. The OC/EC content in the sample was measured by a carbon analyzer (Thermal/Optical, DRI 2001). The annual average concentration of OC and EC was found to be 28.01 ± 14.61 μg/m3 and 10.40 ± 7.41 μg/m3, respectively in PM1 (139.52 ± 49.20 μg/m3). The highest concentrations of OC and EC were observed in the post-monsoon and winter season, respectively. Average OC & EC concentrations in summer, monsoon, post-monsoon, and winter seasons were found to be 22.57 ± 3.72 & 5.51 ± 1.28, 11.70 ± 3.07 & 3.60 ± 0.39, 42.06 ± 7.10 & 11.72 ± 2.45 and 37.28 ± 14.45 & 18.52 ± 6.23 µg/m3, respectively. Total carbonaceous material (TCM) accounted for approximately 40% of PM1 concentration. The annual average OC/EC ratio was observed to be 2.69, which ranged between 1.77 to 5.39. Analysis of carbon subfractions reveals OC3 and EC1 as the dominant fraction suggesting fossil fuel combustion as dominant emission sources. The exposure risk estimated on the basis of inhalation dose was observed very high during the winter season which can adversely affect the health of people. This study also revealed that the emissions from the residential area are the key source of OC and EC, along with PM1.

Predicting carbonaceous aerosols and identifying their source contribution with advanced approaches

Organic carbon (OC) and elemental carbon (EC) play important roles in various atmospheric processes and health effects. Predicting carbonaceous aerosols and identifying source contributions are important steps for further epidemiological study and formulating effective emission control policies. However, we are not aware of any study that examined predictions of OC and EC, and this work is also the first study that attempted to use machine learning and hyperparameter optimization method to predict concentrations of specific aerosol contaminants. This paper describes an investigation of the characteristics and sources of OC and EC in fine particulate matter (PM2.5) from 2005 to 2010 in the City of Taipei. Respective hourly average concentrations of OC and EC were 5.2 μg/m3 and 1.6 μg/m3. We observed obvious seasonal variation in OC but not in EC. Hourly and daily OC and EC concentrations were predicted using generalized additive model and grey wolf optimized multilayer perceptron model, which could explain up to about 80% of the total variation. Subsequent clustering suggests that traffic emission was the major contribution to OC, accounting for about 80% in the spring, 65% in the summer, and 90% in the fall and winter. In the Taipei area, local emissions were the dominant sources of OC and EC in all seasons, and long-range transport had a significant contribution to OC and in PM2.5 in spring.

Wintertime carbonaceous species and trace metals in PM10 in Darjeeling: A high altitude town in the eastern Himalayas

Carbonaceous components [organic carbon (OC), elemental carbon (EC), water soluble organic carbon (WSOC), primary organic carbon (POC), secondary organic carbon (SOC) and carbonaceous aerosols (CAs)] and major and trace elements (Na, Mg, Ca, Al, Fe, Ti, Cl, P, S, K, Cr, Ni, Cu, Zn, Mo and B) of PM10 were studied over the eastern Himalayan high altitude station [Darjeeling: 27.01°N and 88.15°E, 2200 m average mean sea level (amsl)] during winter 2018–19 (December 2018–February 2019). The carbonaceous aerosols/species (CAs) contributed to ~23% of PM10 mass concentration, whereas major and trace elements accounted for 10% of PM10. During the entire study period, the average concentrations of PM10, OC, EC, WSOC, POC, SOC and CAs were recorded as 48 ± 16 μg m−3, 5.39 ± 1.84 μg m−3, 2.60 ± 0.94 μg m−3, 3.87 ± 1.18 μg m−3, 3.40 ± 1.23 μg m−3, 1.99 ± 1.03 μg m−3 and 11.21 ± 3.78 μg m−3, respectively. Significant positive correlation between OC & EC and OC & WSOC have been observed which are indicating their common sources. WSOC/OC ratio was estimated to be 0.71 suggesting that the biomass burning is one of the major sources of carbonaceous aerosols at Darjeeling during winter. The significant positive correlation of PM10 with crustal elements (Al, Fe, Ca, Mg and Ti) as well as the correlation of Al with other crustal elements (Fe, Ca, Mg and Ti) indicates the abundance of mineral dust at the sampling site. Principal component analysis (PCA) identified the contribution of crustal/soil dust, biomass + coal burning, vehicular emissions and solid waste to the PM10 over the eastern Himalayan region of India.

Estimated contribution of vehicular emissions to carbonaceous aerosols in urban Beijing, China

Worldwide attention has been focused on air pollution associated with vehicle emissions. With the highest number of vehicles, Beijing has experienced air pollution related to vehicle emissions. To better recognize the contributions of vehicle emissions to organic carbon (OC) and elemental carbon (EC), hourly measurements of OC and EC in PM2.5 were conducted in urban Beijing from June 1, 2016 to May 31, 2017 in addition to auxiliary measurements of water-soluble ions and elements. The average concentrations of OC and EC were 11.9 ± 11.1 and 3.7 ± 3.6 μg/m3 during the study period, respectively, while those of OC and EC during the nighttime (0:00–6:00), morning rush hour (7:00–9:00) and evening rush hour (17:00–19:00) were 12.9 ± 12.9 μg/m3 and 4.4 ± 4.3 μg/m3, 10.4 ± 9.8 μg/m3 and 3.7 ± 3.1 μg/m3, and 12.3 ± 8.7 μg/m3 and 3.5 ± 2.4 μg/m3, respectively. The diurnal variations in OC and EC concentrations showed higher values during the nighttime, morning rush hour and evening rush hour. Strong correlations were found between OC and CO (r2 = 0.76–0.79) and between OC and NOx (r2 = 0.63–0.68); strong correlations were also found between EC and CO (r2 = 0.76–0.81) and between EC and NOx (r2 = 0.63–0.68) during the nighttime, morning rush hour and evening rush hour. The results of source apportionment based on the hourly PM2.5-associated chemical composition by a positive matrix factorization model showed that vehicle emissions accounted for 23.0% of PM2.5. From the profiles of the source apportionment of PM2.5, it could be found that vehicle emissions contributed 51.2%, 51.3% and 25.2% of the concentrations of OC, EC and PM2.5 on average during the nighttime, respectively. The contributions of vehicle emissions to OC, EC and PM2.5 during the nighttime were higher than or close to those during the evening rush hour and the morning rush hour. This result indicated that vehicular emissions play an important role in carbonaceous aerosols and PM2.5 during the nighttime. The above results provide insight into the quantitative evaluation of the contribution of vehicular emissions to OC, EC and PM2.5 and thus could provide references for pollution control in areas with high vehicular emissions.

Variation of carbonaceous species and trace elements in PM10 at a mountain site in the central Himalayan region of India

Observations of carbonaceous species [organic carbon (OC), elemental carbon (EC), water soluble organic carbon (WSOC), carbonaceous aerosols (CAs) and secondary organic carbon (SOC) ] and trace elements (As, Cr, Ni, Zn, Na, Mg, Al, P, K, Ca, Ti, Fe, and Mn) in PM10 are made over a high altitude site (ARIES, Nainital, 29.4° N, 79.5° E, ~1958 m amsl) in the central Himalayan region during October 2018−February 2019 to explore their possible sources. The average concentrations of PM10, OC, EC, WSOC, CA and SOC were recorded as 44±13 µg m-3, 3.66±1.26 µg m-3, 1.29±0.61 µg m-3, 2.28±0.76 µg m-3, 7.15±1.96 µg m-3 and 1.45±0.73 µg m-3, respectively during the study period. The concentrations of PM10, OC, EC, WSOC, CAs and SOC were significantly varied during autumn (October-November) and winter (December-February) seasons. During both the seasons, significant positive linear trend between OC & EC and OC & WSOC have been observed which is indicative of their common sources of carbonaceous aerosols at the study site. WSOC/OC ratio was estimated as 0.56 and 0.67 during autumn and winter, respectively suggested that the biomass burning could be one of the major sources of carbonaceous aerosols at Nainital. The significant positive correlation of PM10 with crustal elements (Al, Fe, Ca, Mg and Ti) as well as correlation of Al with other crustal elements (Fe, Ca, Mg and Ti) indicates the abundance of mineral dust at the sampling site. The observed Fe/Al ratio (1.07) also indicates mineral dust as a source at the sampling site, similarly, Ca/Al ratio (1.36) indicates that aerosols over this region is rich in Ca mineral as compared to average continental crust. Principal component analysis (PCA) identified the contribution of crustal/soil dust, biomass burning and industrial emissions to the PM10 over the central Himalayan region of India. Five days back trajectory analysis indicates that the air mass impacting the sampling site is from local surrounding area in Uttrakhand as well from Himachal Pradesh, Jammu & Kashmir, Ingo Gangetic Plain (IGP) region, Pakistan, Afghanistan region and Thar Desert.

Chemical characterization and sources of PM2.5 at a high-alpine ecosystem in the Southeast Tibetan Plateau, China

Abstract The study of atmospheric chemical compositions in remote areas is of great significance for understanding the biogeochemical impact of atmospheric dry deposition on ecosystems. In this study, a total of 50 p.m.2.5 samples were collected at a high alpine forest of Mt. Gongga, Eastern Tibetan Plateau from May 2015 to May 2016 to investigate the characteristics of PM2.5 mass concentration and its major compositions including elemental carbon (EC), organic carbon (OC), and 24 trace elements. The average PM2.5 mass concentration was 17.19 ± 8.81 μg/m3, which was at an intermediate level compared with other areas of Tibetan Plateau. The yearly average concentrations of OC and EC were 2.98 ± 1.95 and 0.43 ± 0.33 μg/m3, accounting for 19.49% and 2.51% of PM2.5 mass, respectively, and the sums of the total concentrations of the 24 analyzed trace elements were 3.70 ± 0.80 μg/m3, accounting 27% of PM2.5 mass concentration. PM2.5, EC and OC showed the higher concentrations and larger fluctuation in the dry season (October 2015 to May 2016) compared with those in the wet season (June 2015 to September 2015), which was attributed to the multiple factors including the increases of biomass burning and fossil fuel emissions, the relatively shallow boundary layer height and lower temperature, and the less precipitation. Two distinct seasonal patterns were observed for the 24 analyzed trace elements in PM2.5: the crustal-derived trace elements like Fe, Al, Mn and Sr showed the higher concentrations in the wet season, while anthropogenic-derived elements such as Cd, Pb, Ni and Zn exhibited the higher level during the dry season. Six sources were identified for PM2.5 at Mt. Gongga with the application of the positive matrix factorization (PMF). Biomass burning (27.06%) and crustal source (26.93%) were the two main sources, followed by secondary formation (16.41%), traffic-related source (12.89%), coal burning (10.57%) and industrial metallurgical process (6.15%). Finally, it was proposed that the atmospheric acidic processing could not only promote the dissolution of Fe, but also enhance the solubility of the other trace elements in the atmosphere during the transport. Accordingly, this would increase the bioavailability and/or toxicity to the biotic and plants.