scholarly journals Size-Segregated Atmospheric Humic-Like Substances (HULIS) in Shanghai: Abundance, Seasonal Variation, and Source Identification

Atmosphere ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 526
Author(s):  
Tianming Sun ◽  
Rui Li ◽  
Ya Meng ◽  
Yu Han ◽  
Hanyun Cheng ◽  
...  
Keyword(s):  
Seasonal Variation ◽  
Size Distribution ◽  
Principal Component ◽  
Water Soluble ◽  
Atmospheric Particulate Matter ◽  
Biomass Combustion ◽  
Vehicle Exhaust ◽  
Total Suspended Particulates ◽  
Condensation Mode ◽  
Water Soluble Organic Carbon

Humic-like substances (HULIS) are of great interest due to their optical and chemical characteristics. In this study, a total of 180 samples of atmospheric particulate matter (PM) of different sizes were collected from summer 2018 to spring 2019, in order to analyze the size distribution, to investigate the seasonal variation and then to identify the key sources of HULIS. The annual mean concentration of HULIS in the total suspended particulates reached 5.12 ± 1.42 μg/m3. The HULIS concentration was extremely higher in winter (8.35 ± 2.06 μg/m3) than in autumn (4.88 ± 0.95 μg/m3), in summer (3.62 ± 1.68 μg/m3) and in spring (3.36 ± 0.99 μg/m3). The average annual ratio of water-soluble organic carbon (WSOC) to OC and the ratio of HULIS to WSOC reached 0.546 ± 0.092 and 0.56 ± 0.06, respectively. Throughout the whole year, the size distributions of WSOC and HULIS-C were relatively smooth. The peaks of WSOC appeared at 1.8~3.2 μm and 0.56~1.0 μm, while the peaks of HULIS-C were located at 3.2~5.6 μm, 1.0~1.8 μm and 0.18~0.32 μm. The distribution of the HULIS particle mode was similar in spring, summer and autumn, while there was a lower proportion of the coarse mode and a higher proportion of the condensation mode in winter. By using the comprehensive analysis of principal component analysis (PCA), air mass backward trajectories (AMBTs) and fire point maps, key sources of WSOC and HULIS in Shanghai were identified as biomass combustion (48.42%), coal combustion (17.49%), secondary formation (16.07%) and vehicle exhaust (5.37%). The remaining part might be contributed by crustal dust sources, marine sources and/or other possible sources. This study provides new insight into the characteristics and size distribution of HULIS in Shanghai, thereby providing a practical base for further modeling.

scholarly journals Composition and mass size distribution of nitrated and oxygenated aromatic compounds in ambient particulate matter from southern and central Europe – implications for origin

2019 ◽  
Author(s):  
Zoran Kitanovski ◽  
Pourya Shahpoury ◽  
Constantini Samara ◽  
Aristeidis Voliotis ◽  
Gerhard Lammel
Keyword(s):  
Particulate Matter ◽  
Size Fraction ◽  
Ambient Air ◽  
Water Soluble ◽  
Atmospheric Particulate Matter ◽  
Polycyclic Aromatic ◽  
Mass Size ◽  
Water Soluble Organic Carbon ◽  
Soluble Organic Carbon ◽  
The Individual

Abstract. Nitro-monoaromatic hydrocarbons (NMAHs), such as nitrocatechols, nitrophenols and nitrosalicylic acids, are important constituents of atmospheric particulate matter (PM) water soluble organic carbon (WSOC) and humic-like substances (HULIS). Nitrated and oxygenated derivatives of polycyclic aromatic hydrocarbons (NPAHs, OPAHs) are toxic and ubiquitous in the ambient air; due to their light absorption properties, together with NMAHs they are part of aerosol brown carbon (BrC). We investigated the winter concentrations of these substance classes in size-resolved particulate matter (PM) from two urban sites in central and southern Europe, i.e. Mainz (MZ), Germany and Thessaloniki (TK), Greece. ∑11NMAH concentrations in PM10 and total PM were 0.51–8.38 and 12.1–72.1 ng m−3 at MZ and TK site, respectively, whereas ∑8OPAHs were 47–1636 and 858–4306 pg m−3, and ∑17NPAHs were ≤ 90 and 76–578 pg m−3, respectively. NMAHs and the water-soluble OPAHs contributed 0.4 and 1.8 %, and 0.0001 and 0.0002 % to the HULIS mass, at MZ and TK, respectively. The mass size distributions of the individual substances generally peaked in the smallest or second smallest size fraction i.e.,

scholarly journals Observation and Source Apportionment of Trace Gases, Water-Soluble Ions and Carbonaceous Aerosol During a Haze Episode in Wuhan

Atmosphere ◽  
2019 ◽  
Vol 10 (7) ◽  
pp. 397 ◽  
Author(s):  
Zhengxu Gao ◽  
Xiaoling Wang ◽  
Lijuan Shen ◽  
Hua Xiang ◽  
Honglei Wang
Keyword(s):  
Organic Carbon ◽  
Air Pollutants ◽  
Principal Component ◽  
Water Soluble ◽  
Vehicle Exhaust ◽  
Soluble Ions ◽  
Secondary Formation ◽  
Water Soluble Ions ◽  
Haze Episode ◽  
Haze Days

As the new core region of the haze pollution, the terrain effect of sub-basin and water networks over the Twin-Hu Basin (THB) in the Yangtze River Middle-Reach (YRMR) had great impacts on the variations and distributions of air pollutants. In this study, trace gases (NH3, HNO3, and HCl), water-soluble ions (WSIs), organic carbon (OC), and elemental carbon (EC) were measured in PM2.5 from 9 January to 27 January 2018, in Wuhan using monitoring for aerosols and gases (MARGA) and a semi-continuous OC/EC analyzer (Model RT-4). The characteristics of air pollutants during a haze episode were discussed, and the PM2.5 sources were quantitatively analyzed on haze and non-haze days using the principal component analysis/absolute principal component scores (PCA/APCS) model. The average PM2.5 concentration was 122.61 μg·m−3 on haze days, which was 2.20 times greater than it was on non-haze days. The concentrations of secondary water soluble ions (WSIs) including NO3−, SO42−, and NH4+ increased sharply on haze days, which accounted for 91.61% of the total WSIs and were 2.43 times larger than the values on non-haze days. The heterogeneous oxidation reactions of NO2 and SO2 during haze episodes were proven to be the major sources of sulfate and nitrate in PM2.5. On haze days, the concentrations of EC, primary organic carbon (POC), and secondary organic carbon (SOC) were 1.68, 1.69, and 1.34 times larger than those on non-haze days, the CO, HNO3, and NH3 concentrations enhanced and relatively low SO2, O3, and HNO2 levels were observed on haze days. The diurnal variations of different pollutants distinctly varied on haze days. The PM2.5 in Wuhan primarily originated from the secondary formation, combustion, dust, industry, and vehicle exhaust sources. The source contributions of the secondary formation + combustion sources to PM2.5 on haze days were 2.79 times larger than the level on non-haze days. The contribution of the vehicle exhaust + combustion source on haze days were 0.59 times the value on non-haze days. This description is supported by a summary of how pollutant concentrations and patterns vary in the THB compared to the variations in other pollution regions in China, which have been more completely described.

scholarly journals Characteristics of Carbonaceous PM2.5 in a Small Residential City in Korea

Atmosphere ◽  
2018 ◽  
Vol 9 (12) ◽  
pp. 490 ◽  
Author(s):  
Jong-Min Park ◽  
Young-Ji Han ◽  
Sung-Hwan Cho ◽  
Hyun-Woong Kim
Keyword(s):  
Organic Carbon ◽  
Strong Correlation ◽  
Sampling Period ◽  
Ambient Air ◽  
Quality Standard ◽  
Water Soluble ◽  
Biomass Combustion ◽  
Polycyclic Aromatic ◽  
Water Soluble Organic Carbon ◽  
Ambient Air Quality Standard

PM2.5 has been a serious issue in South Korea not only in urban and industrial areas but also in rural and background areas. In this study, PM2.5 and its carbonaceous compounds including organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC), and polycyclic aromatic hydrocarbons (PAHs) were collected and analyzed in a small residential city. The PM2.5 concentration frequently exceeded the national ambient air quality standard during the spring and the winter, which often occurred concurrently with fog and mist events. Over the whole sampling period, both OC and the OC/EC ratio were considerably higher than the ratios in other cities in Korea, which suggests that sources other than vehicular emissions were important. The top 10% of OC/EC ratio samples could be explained by regional and long-range transport because there was a strong correlation between primary and secondary organic carbon. However, biomass combustion was likely to account for the consistently high OC concentration due to a strong correlation between WSOC and primary OC as well as the diagnostic ratio results of PAHs.

scholarly journals Size-Segregated Characteristics of Carbonaceous Aerosols during the Monsoon and Non-Monsoon Seasons in Lhasa in the Tibetan Plateau

Atmosphere ◽  
2019 ◽  
Vol 10 (3) ◽  
pp. 157 ◽  
Author(s):  
Nannan Wei ◽  
Chulei Ma ◽  
Junwen Liu ◽  
Guanghua Wang ◽  
Wei Liu ◽  
...  
Keyword(s):  
Tibetan Plateau ◽  
Organic Carbon ◽  
Size Distribution ◽  
Fossil Fuels ◽  
Monsoon Season ◽  
Water Soluble ◽  
Atmospheric Particulate Matter ◽  
The Tibetan Plateau ◽  
Carbonaceous Aerosols ◽  
Different Diameters

In this paper, we intensively collected atmospheric particulate matter (PM) with different diameters (size ranges: <0.49, 0.49–0.95, 0.95–1.5, 1.5–3.0, 3.0–7.2, and >7.2 μm) in Lhasa during the monsoon and non-monsoon seasons. The results clearly showed that the concentrations of PM, organic carbon (OC), elemental carbon (EC), and water-soluble organic carbon (WSOC) during the non-monsoon season were much higher than the concentrations during the monsoon season. During the monsoon season, a bimodal size distribution of the OC and WSOC, which were at <0.49 μm and >7.2 μm, respectively, and a unimodal size distribution at <0.49 μm for the EC were observed. However, during the non-monsoon season, there was a trimodal size distribution of the OC and WSOC (<0.49 μm, 1.5–3.0 μm, and >7.2 μm), and a unimodal size distribution of the EC (<0.49 μm). Possible sources of the carbonaceous components were revealed by combining the particle size distribution and the correlation analysis. OC, EC, and WSOC were likely from the photochemical transformation of biogenic and anthropogenic VOC, and the incomplete combustion of biomass burning and fossil fuels at <0.49 μm, whilst they were also likely to be from various types of dust and biogenic aerosols at >7.2 μm. OC and WSOC at 1.5–3.0 μm were likely to have been from the burning of yak dung and photochemical formation. The above results may draw attention in the public and scientific communities to the issues of air quality in the Tibetan Plateau.

Size and Composition of Ambient Particulates in the Yueguangshan-Tunnel, Taiwan

2013 ◽  
Vol 726-731 ◽  
pp. 2074-2078 ◽  
Author(s):  
Mei Fang Lu ◽  
Mei Chuan Huang ◽  
Kuang Hung Cheng ◽  
Jim Jui Min Lin
Keyword(s):  
Particulate Matter ◽  
Size Distribution ◽  
Average Concentration ◽  
Exhaust Emission ◽  
Vehicle Exhaust ◽  
Average Mass ◽  
Total Suspended Particulates ◽  
Coarse Particulate Matter ◽  
Air Ventilation ◽  
Mass Size

The aim of this study is to investigate the characteristics of size distribution and chemical composition of ambient particulates inside a tunnel. Inside the tunnel, the average concentration of PM2.5and PM2.5-10was 479 and 444 μg/m3respectively. The average mass-size distribution showed a trimodal distribution (25-30, 4.0-5.0, and 2.5, PM2.5-10, and PM>10were 25%, 40%, and 35% of the total suspended particulates. Because of the poor air ventilation inside the tunnel, the particulates accumulate inside the tunnel. The dominated species of PM2.5were EC (average concentration 122.91 μg/m3, 25.78%), OC (47.68 μg/m3, 10.53%), SO42-(37.42 μg/m3, 8.24%), and NO3-(35.01 μg/m3, 7.95%), and were EC ( 131.77 μg/m3, 29.87%), OC (53.74 μg/m3, 12.15%), SO42-(31.35 μg/m3, 7.11%), and NO3-(28.10 μg/m3, 6.42%) for PM2.5-10. Results from this study showed that the concentrations of coarse particulate matter and several metals are apparently dominated by re-suspended matter rather than emissions from vehicles, e.g., Al, Ca, and Fe. Therefore, ambient particulate matter is caused by not only vehicle exhaust emission but also dusty roads and traffic-generated dust.

scholarly journals Desiccation time and rainfall control gaseous carbon fluxes in an intermittent stream

2021 ◽  
Author(s):  
Maria Isabel Arce ◽  
Mia M. Bengtsson ◽  
Daniel von Schiller ◽  
Dominik Zak ◽  
Jana Täumer ◽  
...  
Keyword(s):  
Water Soluble ◽  
Intermittent Flow ◽  
Dry Period ◽  
Intermittent Stream ◽  
Aerobic Activity ◽  
Water Soluble Organic Carbon ◽  
Soluble Organic Carbon ◽  
Microbial C ◽  
Global Biogeochemical Cycles ◽  
The Impact

AbstractDroughts are recognized to impact global biogeochemical cycles. However, the implication of desiccation on in-stream carbon (C) cycling is not well understood yet. We subjected sediments from a lowland, organic rich intermittent stream to experimental desiccation over a 9-week-period to investigate temporal changes in microbial functional traits in relation to their redox requirements, carbon dioxide (CO2) and methane (CH4) fluxes and water-soluble organic carbon (WSOC). Concurrently, the implications of rewetting by simulated short rainfalls (4 and 21 mm) on gaseous C fluxes were tested. Early desiccation triggered dynamic fluxes of CO2 and CH4 with peak values of 383 and 30 mg C m−2 h−1 (mean ± SD), respectively, likely in response to enhanced aerobic mineralization and accelerated evasion. At longer desiccation, CH4 dropped abruptly, likely because of reduced abundance of anaerobic microbial traits. The CO2 fluxes ceased later, suggesting aerobic activity was constrained only by extended desiccation over time. We found that rainfall boosted fluxes of CO2, which were modulated by rainfall size and the preceding desiccation time. Desiccation also reduced the amount of WSOC and the proportion of labile compounds leaching from sediment. It remains questionable to which extent changes of the sediment C pool are influenced by respiration processes, microbial C uptake and cell lysis due to drying-rewetting cycles. We highlight that the severity of the dry period, which is controlled by its duration and the presence of precipitation events, needs detailed consideration to estimate the impact of intermittent flow on global riverine C fluxes.

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