scholarly journals Boron Isotopic Analysis of Representative Atmospheric Aerosols Derived From Long-Range Transported/Local Emission on an Islet Offshore NE Taiwan

2021 ◽  
Vol 9 ◽  
Author(s):  
Yen-Po Lin ◽  
Chen-Feng You ◽  
Tsung-Yu Kao ◽  
Chuan-Hsiung Chung ◽  
Chung-Chieh Gary Hung
Keyword(s):  
Long Range ◽  
Atmospheric Aerosols ◽  
Isotopic Analysis ◽  
Water Soluble ◽  
Human Perturbation ◽  
Anthropogenic Contributions ◽  
Aerosol Emissions ◽  
Local Emissions ◽  
Air Mass Origin ◽  
Northern Taiwan

To identify pollutant origins and their potential sources from either long-range transported (LRT) or local emissions, the Boron (B) concentrations and the B isotopic compositions (δ11B) in the water-soluble fraction of aerosols were determined. These aerosols were collected from an islet offshore in northeastern Taiwan, Peng Chia Yu (PCY), a non-residential islet, from January 1998 to March 2000. This islet may be influenced by various pollutants or chemical transport during monsoon periods, but suffers minimal human perturbation locally. The B in the specimens falls to 0.3–1.63 ng m−3 during the SW monsoon seasons when compared to 0.46–2.56 ng m−3 in the NE monsoon. However, the δ11B results show no clear variations in both monsoon seasons (10.7–24.3‰), regardless of differences in air mass origin. A two end-member mixing scenario is proposed to explain our observations using the obtained δ11B and 1/[B] results. The ocean endmember is characterized by high 1/[B] and high δ11B; while other endmember is from continental endmember or anthropogenic contributions that are characterized by of 1/[B] and lowδ11B (δ11B < 10‰). Based on these chemical and isotopic results, we found aerosol emissions in northern Taiwan are characterized as low B with nearly constant δ11B, when compared with long-range transported continental endmembers derived from nearby regions. This study provides preliminary B and δ11B levels in aerosols derived from LRT/local emissions and discusses potential monsoonal effects on aerosols offshore of NE Taiwan.

scholarly journals Sources of anions in aerosols in northeast Greenland during late winter

2012 ◽  
Vol 12 (6) ◽  
pp. 14813-14836 ◽  
Author(s):  
M. Fenger ◽  
L. L. Sørensen ◽  
K. Kristensen ◽  
B. Jensen ◽  
Q. T. Nquyen ◽  
...  
Keyword(s):  
Sea Ice ◽  
Long Range ◽  
Atmospheric Aerosols ◽  
Fine Particles ◽  
Chemical Properties ◽  
High Arctic ◽  
Early Spring ◽  
Water Soluble ◽  
The Arctic ◽  
Late Winter

Abstract. The knowledge of climate effects of atmospheric aerosols is associated with large uncertainty, and a better understanding of their physical and chemical properties is needed, especially in the Arctic environment. The objective of the present study is to improve our understanding of the processes affecting the composition of the aerosols in the high Arctic. Therefore size-segregated aerosols were sampled at a high Arctic site, Station Nord (Northeast Greenland), in March 2009 using a Micro Orifice Uniform Deposit Impactor. The aerosol samples were extracted in order to analyze the three water-soluble anions: chloride, nitrate and sulphate. The results are discussed based on possible chemical and physical transformations as well as transport patterns. The total concentrations of the ions at Station Nord were 53–507 ng m−3, 2–298 ng m−3 and 535–1087 ng m−3 for chloride (Cl−), nitrate (NO3-) and sulphate (SO42−), respectively. The aerosols in late winter/early spring, after polar sunrise, are found to be a mixture of long-range transported and regional to local originating aerosols. Fine particles, smaller than 1 μm, containing SO42−, Cl− and NO3−, are hypothesized to originate from long-range transport, where SO42− is by far the dominating anion accounting for 50–85% of the analyzed mass. The analysis suggests that Cl− and NO3− in coarser particles (>1.5 μm) originate from local/regional sources. Under conditions where the air mass is transported over sea-ice at high wind speeds, very coarse particles (>18 μm) are observed and it is hypothesized that frost flowers on the sea ice is a source of very coarse chloride particles in the Arctic.

scholarly journals Sources of anions in aerosols in northeast Greenland during late winter

2013 ◽  
Vol 13 (3) ◽  
pp. 1569-1578 ◽  
Author(s):  
M. Fenger ◽  
L. L. Sørensen ◽  
K. Kristensen ◽  
B. Jensen ◽  
Q. T. Nguyen ◽  
...  
Keyword(s):  
Sea Ice ◽  
Long Range ◽  
Atmospheric Aerosols ◽  
Fine Particles ◽  
Chemical Properties ◽  
High Arctic ◽  
Early Spring ◽  
Water Soluble ◽  
The Arctic ◽  
Late Winter

Abstract. The knowledge of climate effects of atmospheric aerosols is associated with large uncertainty, and a better understanding of their physical and chemical properties is needed, especially in the Arctic environment. The objective of the present study is to improve our understanding of the processes affecting the composition of aerosols in the high Arctic. Therefore size-segregated aerosols were sampled at a high Arctic site, Station Nord (Northeast Greenland), in March 2009 using a Micro Orifice Uniform Deposit Impactor. The aerosol samples were extracted in order to analyse three water-soluble anions: chloride, nitrate and sulphate. The results are discussed based on possible chemical and physical transformations as well as transport patterns. The total concentrations of the ions at Station Nord were 53–507 ng m−3, 2–298 ng m−3 and 535–1087 ng m−3 for chloride (Cl−), nitrate (NO3−) and sulphate (SO42−), respectively. The aerosols in late winter/early spring, after polar sunrise, are found to be a mixture of long-range transported and regional to local originating aerosols. Fine particles, smaller than 1 μm, containing SO42−, Cl− and NO3−, are hypothesized to originate from long-range transport, where SO42− is by far the dominating anion accounting for 50–85% of the analyzed mass. The analysis suggests that Cl− and NO3− in coarser particles (> 1.5 μm) originate from local/regional sources. Under conditions where the air mass is transported over sea ice at high wind speeds, very coarse particles (> 18 μm) are observed, and it is hypothesized that frost flowers on the sea ice are a source of the very coarse nitrate particles.

scholarly journals Characteristics, seasonality and sources of carbonaceous and ionic components in the tropical Indian aerosols

2011 ◽  
Vol 11 (2) ◽  
pp. 3937-3976 ◽  
Author(s):  
C. M. Pavuluri ◽  
K. Kawamura ◽  
S. G. Aggarwal ◽  
T. Swaminathan
Keyword(s):  
Organic Carbon ◽  
Atmospheric Aerosols ◽  
Atmospheric Transport ◽  
Indian Subcontinent ◽  
Ionic Species ◽  
Water Soluble ◽  
Carbonaceous Aerosols ◽  
Mass Fractions ◽  
High Concentrations ◽  
Ionic Components

Abstract. To better characterize South and Southeast Asian aerosols, PM10 samples collected from tropical Chennai, India (13.04° N; 80.17° E) were analyzed for carbonaceous and water-soluble ionic components. Concentration ranges of elemental carbon (EC) and organic carbon (OC) were 2.4–14 μg m−3 and 3.2–15.6 μg m−3 in winter samples whereas they were 1.1–2.5 μg m−3 and 4.1–17.6 μg m−3 in summer samples, respectively. Concentration of secondary organic carbon (SOC) retrieved from EC-tracer method was 4.6 ± 2.8 μg m−3 in winter and 4.3 ± 2.8 μg m−3 in summer. SO42- (8.8 ± 2.5 μg m−3 and 4.1 ± 2.7 μg m−3 in winter and summer, respectively) was found as the most abundant ionic species (57% on average, n = 49), followed by NH4+ (15%) > NO3− > Cl− > K+> Na+ > Ca2+ > MSA− > Mg2+. The mass fractions of EC, organic matter (OM) and ionic species varied seasonally, following the air mass trajectories and corresponding source strength. Based on mass concentration ratios of selected components and relations of EC and OC to marker species, we found that biofuel/biomass burning is the major source of atmospheric aerosols in South and Southeast Asia. The high concentrations of SOC and WSOC/OC ratios (ave. 0.45; n = 49) as well as good correlations between SOC and WSOC suggest that the secondary production of organic aerosols during long-range atmospheric transport is also significant in this region. This study provides the baseline data of carbonaceous aerosols for southern part of the Indian subcontinent.

Seasonal variation of water-soluble ion species in the atmospheric aerosols at the summit of Mt. Fuji

2008 ◽  
Vol 42 (34) ◽  
pp. 8027-8035 ◽  
Author(s):  
Issei Suzuki ◽  
Kazuhiko Hayashi ◽  
Yasuhito Igarashi ◽  
Hiroshi Takahashi ◽  
Yousuke Sawa ◽  
...  
Keyword(s):  
Seasonal Variation ◽  
Atmospheric Aerosols ◽  
Water Soluble ◽  
Ion Species ◽  
Soluble Ion

scholarly journals Retrieval of desert dust and carbonaceous aerosol emissions over Africa from POLDER/PARASOL products generated by the GRASP algorithm

2018 ◽  
Vol 18 (16) ◽  
pp. 12551-12580 ◽  
Author(s):  
Cheng Chen ◽  
Oleg Dubovik ◽  
Daven K. Henze ◽  
Tatyana Lapyonak ◽  
Mian Chin ◽  
...  
Keyword(s):  
Optical Depth ◽  
Atmospheric Aerosols ◽  
Carbonaceous Aerosol ◽  
Desert Dust ◽  
Modelling Framework ◽  
Aerosol Absorption ◽  
Modelling Studies ◽  
Distribution Composition ◽  
Gocart Model ◽  
Aerosol Emissions

Abstract. Understanding the role atmospheric aerosols play in the Earth–atmosphere system is limited by uncertainties in the knowledge of their distribution, composition and sources. In this paper, we use the GEOS-Chem based inverse modelling framework for retrieving desert dust (DD), black carbon (BC) and organic carbon (OC) aerosol emissions simultaneously. Aerosol optical depth (AOD) and aerosol absorption optical depth (AAOD) retrieved from the multi-angular and polarimetric POLDER/PARASOL measurements generated by the GRASP algorithm (hereafter PARASOL/GRASP) have been assimilated. First, the inversion framework is validated in a series of numerical tests conducted with synthetic PARASOL-like data. These tests show that the framework allows for retrieval of the distribution and strength of aerosol emissions. The uncertainty of retrieved daily emissions in error free conditions is below 25.8 % for DD, 5.9 % for BC and 26.9 % for OC. In addition, the BC emission retrieval is sensitive to BC refractive index, which could produce an additional factor of 1.8 differences for total BC emissions. The approach is then applied to 1 year (December 2007 to November 2008) of data over the African and Arabian Peninsula region using PARASOL/GRASP spectral AOD and AAOD at six wavelengths (443, 490, 565, 670, 865 and 1020 nm). Analysis of the resulting retrieved emissions indicates 1.8 times overestimation of the prior DD online mobilization and entrainment model. For total BC and OC, the retrieved emissions show a significant increase of 209.9 %–271.8 % in comparison to the prior carbonaceous aerosol emissions. The model posterior simulation with retrieved emissions shows good agreement with both the AOD and AAOD PARASOL/GRASP products used in the inversion. The fidelity of the results is evaluated by comparison of posterior simulations with measurements from AERONET that are completely independent measurements and more temporally frequent than PARASOL observations. To further test the robustness of our posterior emissions constrained using PARASOL/GRASP, the posterior emissions are implemented in the GEOS-5/GOCART model and the consistency of simulated AOD and AAOD with other independent measurements (MODIS and OMI) demonstrates promise in applying this database for modelling studies.

Investigation of atmospheric aerosols over semi-urban and urban areas in Eastern Indo-Gangetic Plain: seasonal variability and source apportionment using PMF

2021 ◽  
Author(s):  
Kanishtha Dubey ◽  
Shubha Verma
Keyword(s):  
Organic Carbon ◽  
Biomass Burning ◽  
Atmospheric Aerosols ◽  
Urban Areas ◽  
Relative Concentration ◽  
Road Dust ◽  
Water Soluble ◽  
Carbonaceous Aerosols ◽  
Gangetic Plain ◽  
Brick Kilns

<p>The study investigates the chemical composition and source of aerosol origin at a semi-urban (Kharagpur–Kgp) and urban (Kolkata–Kol) region during the period February 2015 to January 2016 and September 2010 to August 2011 respectively. Major water-soluble inorganic aerosols (WSII) were determined using Ion chromatography and carbonaceous aerosols (CA) using OC–EC analyser. A multivariate factor analysis Positive Matrix Factorization (PMF) was used in resolving source of aerosols at the study locations. Seasonal analysis of WSII at Kgp and Kol indicated relative dominance of calcium at both the places followed by sodium, chloride, and magnesium ions. Non-sea salt potassium (nss–K<sup>+</sup>), a biomass burning tracer was found higher at Kol than at Kgp. Sum of secondary aerosols sulphate (SO<sub>4</sub><sup>2-</sup>), nitrate (NO<sub>3</sub><sup>-</sup>) and ammonium (NH<sub>4</sub><sup>+</sup>) was higher at Kol than Kgp with relative concentration of SO<sub>4</sub><sup>2-</sup> being higher than NO<sub>3</sub><sup>-</sup> at Kgp which was vice-versa at Kol. Examination of carbonaceous aerosols showed three times higher concentration of organic carbon (OC) than elemental carbon (EC) with monthly mean of OC/EC ratio > 2, indicating likely formation of secondary organic carbon formation. Seasonal influence of biomass burning inferred from nss–K<sup>+</sup> (OC/EC) ratio relationship indicated dissimilarity in seasonality of biomass burning at Kgp (Kol). PMF resolved sources for Kgp constituted of secondary aerosol emissions, biomass burning, fugitive dust, marine aerosols, crustal dust and emissions from brick kilns while for Kol factors constituted of burning of waste, resuspended paved road dust, coal combustion, sea spray aerosols, vehicular emissions and biomass burning.</p>

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