Sources and Radiative Absorption of Water‐Soluble Brown Carbon in the High Arctic Atmosphere

2019 ◽  
Vol 46 (24) ◽  
pp. 14881-14891 ◽  
Author(s):  
Siyao Yue ◽  
Srinivas Bikkina ◽  
Meng Gao ◽  
Leonard A. Barrie ◽  
Kimitaka Kawamura ◽  
...  
Keyword(s):  
High Arctic ◽  
Water Soluble ◽  
Brown Carbon ◽  
Arctic Atmosphere ◽  
Radiative Absorption

scholarly journals Fluorescent water-soluble organic aerosols in the High Arctic atmosphere

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Pingqing Fu ◽  
Kimitaka Kawamura ◽  
Jing Chen ◽  
Mingyue Qin ◽  
Lujie Ren ◽  
...  
Keyword(s):  
Organic Aerosols ◽  
High Arctic ◽  
Water Soluble ◽  
Arctic Atmosphere

Brown carbon in the continental outflow to the North Indian Ocean

2019 ◽  
Vol 21 (6) ◽  
pp. 970-987 ◽  
Author(s):  
Srinivas Bikkina ◽  
Manmohan Sarin
Keyword(s):  
Indian Ocean ◽  
Soluble Fraction ◽  
North Indian Ocean ◽  
Water Soluble ◽  
Gangetic Plain ◽  
Brown Carbon ◽  
Water Soluble Fraction ◽  
The North ◽  
Continental Outflow ◽  
Indo Gangetic Plain

In this paper, we synthesize the size distribution and optical properties of the atmospheric water-soluble fraction of light-absorbing organic carbon (brown carbon; BrC) in the continental outflow from the Indo-Gangetic Plain (IGP) in South Asia to the North Indian Ocean.

Light absorption properties of elemental carbon (EC) and water-soluble brown carbon (WS–BrC) in the Kathmandu Valley, Nepal: A 5-year study

2020 ◽  
Vol 261 ◽  
pp. 114239 ◽  
Author(s):  
Pengfei Chen ◽  
Shichang Kang ◽  
Lekhendra Tripathee ◽  
Kirpa Ram ◽  
Maheswar Rupakheti ◽  
...  
Keyword(s):  
Light Absorption ◽  
Elemental Carbon ◽  
Water Soluble ◽  
Kathmandu Valley ◽  
Absorption Properties ◽  
Brown Carbon

scholarly journals Chemical and optical properties of carbonaceous aerosols in Nanjing, eastern China: regionally transported biomass burning contribution

2019 ◽  
Vol 19 (17) ◽  
pp. 11213-11233 ◽  
Author(s):  
Xiaoyan Liu ◽  
Yan-Lin Zhang ◽  
Yiran Peng ◽  
Lulu Xu ◽  
Chunmao Zhu ◽  
...  
Keyword(s):  
Optical Properties ◽  
Organic Carbon ◽  
Solar Energy ◽  
Energy Absorption ◽  
Biomass Burning ◽  
Eastern China ◽  
Water Soluble ◽  
Carbonaceous Aerosols ◽  
Southeastern China ◽  
Brown Carbon

Abstract. Biomass burning can significantly impact the chemical and optical properties of carbonaceous aerosols. Here, the biomass burning impacts were studied during wintertime in a megacity of Nanjing, eastern China. The high abundance of biomass burning tracers such as levoglucosan (lev), mannosan (man), galactosan (gal) and non-sea-salt potassium (nss-K+) was found during the studied period with the concentration ranges of 22.4–1476 ng m−3, 2.1–56.2 ng m−3, 1.4–32.2 ng m−3 and 0.2–3.8 µg m−3, respectively. The significant contribution of biomass burning to water-soluble organic carbon (WSOC; 22.3±9.9 %) and organic carbon (OC; 20.9±9.3 %) was observed in this study. Backward air mass origin analysis, potential emission sensitivity of elemental carbon (EC) and MODIS fire spot information indicated that the elevations of the carbonaceous aerosols were due to the transported biomass-burning aerosols from southeastern China. The characteristic mass ratio maps of lev∕man and lev∕nss-K+ suggested that the biomass fuels were mainly crop residuals. Furthermore, the strong correlation (p < 0.01) between biomass burning tracers (such as lev) and light absorption coefficient (babs) for water-soluble brown carbon (BrC) revealed that biomass burning emissions played a significant role in the light-absorption properties of carbonaceous aerosols. The solar energy absorption due to water-soluble brown carbon and EC was estimated by a calculation based on measured light-absorbing parameters and a simulation based on a radiative transfer model (RRTMG_SW). The solar energy absorption of water-soluble BrC in short wavelengths (300–400 nm) was 0.8±0.4 (0.2–2.3) W m−2 (figures in parentheses represent the variation range of each parameter) from the calculation and 1.2±0.5 (0.3–1.9) W m−2 from the RRTMG_SW model. The absorption capacity of water-soluble BrC accounted for about 20 %–30 % of the total absorption of EC aerosols. The solar energy absorption of water-soluble BrC due to biomass burning was estimated as 0.2±0.1 (0.0–0.9) W m−2, considering the biomass burning contribution to carbonaceous aerosols. Potential source contribution function model simulations showed that the solar energy absorption induced by water-soluble BrC and EC aerosols was mostly due to the regionally transported carbonaceous aerosols from source regions such as southeastern China. Our results illustrate the importance of the absorbing water-soluble brown carbon aerosols in trapping additional solar energy in the low-level atmosphere, heating the surface and inhibiting the energy from escaping the atmosphere.

scholarly journals Measurement Report: Optical properties and sources of water-soluble brown carbon in Tianjin, North China: insights from organic molecular compositions

2022 ◽  
Author(s):  
Junjun Deng ◽  
Hao Ma ◽  
Xinfeng Wang ◽  
Shujun Zhong ◽  
Zhimin Zhang ◽  
...  
Keyword(s):  
Optical Properties ◽  
Biomass Burning ◽  
Light Absorption ◽  
Radiative Forcing ◽  
North China ◽  
Water Soluble ◽  
Formation Mechanisms ◽  
Chemical Compositions ◽  
Brown Carbon ◽  
Near Ultraviolet

Abstract. Brown carbon (BrC) aerosols exert vital impacts on climate change and atmospheric photochemistry due to their light absorption in the wavelength range from near-ultraviolet (UV) to visible light. However, the optical properties and formation mechanisms of ambient BrC remain poorly understood, limiting the estimation of their radiative forcing. In the present study, fine aerosols (PM2.5) were collected during 2016–2017 on a day/night basis over urban Tianjin, a megacity in North China, to obtain seasonal and diurnal patterns of atmospheric water-soluble BrC. There were obvious seasonal but no evident diurnal variations in light absorption properties of BrC. In winter, BrC showed much stronger light absorbing ability since mass absorption efficiency at 365 nm (MAE365) (1.54 ± 0.33 m2 g−1), which was 1.8 times larger than that (0.84 ± 0.22 m2 g−1) in summer. Direct radiative effects by BrC absorption relative to black carbon in the UV range were 54.3 ± 16.9 % and 44.6 ± 13.9 %, respectively. In addition, five fluorescent components in BrC, including three humic-like fluorophores and two protein-like fluorophores were identified with excitation-emission matrix fluorescence spectrometry and parallel factor (PARAFAC) analysis. The lowly-oxygenated components contributed more to winter and nighttime samples, while more-oxygenated components increased in summer and daytime samples. The higher humification index (HIX) together with lower biological index (BIX) and fluorescence index (FI) suggest that the chemical compositions of BrC were associated with a high aromaticity degree in summer and daytime due to photobleaching. Fluorescent properties indicate that wintertime BrC were predominantly affected by primary emissions and fresh secondary organic aerosol (SOA), while summer ones were more influenced by aging processes. Results of source apportionments using organic molecular compositions of the same set of aerosols reveal that fossil fuel combustion and aging processes, primary bioaerosol emission, biomass burning, and biogenic and anthropogenic SOA formation were the main sources of BrC. Biomass burning contributed much larger to BrC in winter and at nighttime, while biogenic SOA contributed more in summer and at daytime. Especially, our study highlights that primary bioaerosol emission is an important source of BrC in urban Tianjin in summer.

scholarly journals Size-resolved measurements of brown carbon and estimates of their contribution to ambient fine particle light absorption based on water and methanol extracts

2013 ◽  
Vol 13 (7) ◽  
pp. 18233-18276 ◽  
Author(s):  
J. Liu ◽  
M. Bergin ◽  
H. Guo ◽  
L. King ◽  
N. Kotra ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Light Absorption ◽  
Fine Particle ◽  
Elemental Carbon ◽  
Fine Particles ◽  
Water Soluble ◽  
Rural Site ◽  
Brown Carbon ◽  
Methanol Extracts ◽  
Carbon Absorption

Abstract. Light absorbing organic carbon, often termed brown carbon, has the potential to significantly contribute to the visible light absorption budget, particularly at shorter wavelengths. Currently, the relative contributions of particulate brown carbon to light absorption, as well as the sources of brown carbon are poorly understood. With this in mind field measurements were made at both urban (Atlanta), and rural (Yorkville) sites in Georgia. Measurements in Atlanta were made at both a central site and a road side site adjacent to a main highway near the city center. Fine particle brown carbon optical absorption is estimated based on Mie calculations using direct size resolved measurements of chromophores in filter extracts. Size-resolved atmospheric aerosol samples were collected using a cascade impactor and analyzed for water-soluble organic carbon (WSOC), organic and elemental carbon (OC and EC), and solution light absorption spectra of water and methanol extracts. Methanol extracts were more light-absorbing than water extracts for all size ranges and wavelengths. Absorption refractive indices of the organic extracts were calculated from solution measurements for a range of wavelengths and used with Mie theory to predict the light absorption by fine particles comprised of these components, under the assumption that brown carbon and other aerosol components were externally mixed. For all three sites, chromophores were predominately in the accumulation mode with an aerodynamic mean diameter of 0.5 μm, an optically effective size range resulting in predicted particle light absorption being a factor of 2 higher than bulk solution absorption. Fine particle absorption was also measured with a Multi-Angle Absorption Photometer (MAAP) and seven-wavelength Aethalometer. Scattering-corrected aethalometer and MAAP absorption were in good agreement at 670 nm and Mie-estimated absorption based on size-resolved EC data were within 30% of these optical instruments. When applied to solution measurements, at all sites, Mie-predicted brown carbon absorption at 350 nm contributed a significant fraction (20 to 40%) relative to total light absorption, with highest contributions at the rural site where organic to elemental carbon ratios were highest. Brown carbon absorption, however, was highest by the roadside site due to vehicle emissions. The multi-wavelength aethalometer did not detect brown carbon, having an absorption Ångstrom exponent near one. Although the results are within the estimated Aethalometer uncertainties, the direct measurement of brown carbon in solution definitively shows that it is present and this Mie analysis suggests it is optically important in the near UV range in both a rural and urban environment during summer when biomass burning emissions are low.

scholarly journals Water-Soluble Brown Carbon in Atmospheric Aerosols from Godavari (Nepal), a Regional Representative of South Asia

2019 ◽  
Vol 53 (7) ◽  
pp. 3471-3479 ◽  
Author(s):  
Guangming Wu ◽  
Kirpa Ram ◽  
Pingqing Fu ◽  
Wan Wang ◽  
Yanlin Zhang ◽  
...  
Keyword(s):  
South Asia ◽  
Atmospheric Aerosols ◽  
Water Soluble ◽  
Brown Carbon

Brown Carbon Sources in Singapore Identified by Factor Analysis of Atmospheric Pressure Chemical Ionization Mass Spectra

2021 ◽  
Author(s):  
LiuDongQing Yang ◽  
Xianfeng Wang ◽  
Mikinori Kuwata Kuwata
Keyword(s):  
Atmospheric Pressure ◽  
Chemical Ionization ◽  
Atmospheric Pressure Chemical Ionization ◽  
Molecular Ions ◽  
Water Soluble ◽  
Ionization Mass ◽  
Combustion Source ◽  
Brown Carbon ◽  
Pressure Chemical Ionization ◽  
Pressure Chemical

&lt;p&gt;Brown carbon (BrC) is an important candidate for the direct radiative effects of aerosol particles. It has been demonstrated that positive matrix factorization (PMF) is useful in analyzing Aerosol Mass Spectrometer (AMS) data for BrC source apportionment. However, fragmentation of molecular ions in AMS has been limiting its capability to categorize BrC sources. Soft-ionization mass spectrometric techniques are known to retain molecular information of chemical species. In this study, we applied atmospheric pressure chemical ionization mass spectrometry (APCI-MS) to identify the sources of water-soluble BrC. PM2.5 filter samples were collected at a site in Singapore during March-May of 2019. The extracted water-soluble organic matter (WSOM) was analyzed using APCI-MS, time-of-flight aerosol chemical speciation monitor (ToF-ACSM) and ultraviolet-visible spectrophotometer (UV-Vis). Five factor components were obtained by PMF analysis of the APCI-MS data. The PMF output and UV-Vis data were subsequently used to estimate the absorption &amp;#197;ngstrom exponents (AAE) of WSOM in each component. The estimated values of AAE ranged from 3.95 to 8.71. When comparing the factor contributions with simultaneously monitored gas and aerosol data, we found that the factor with the lowest value of AAE was likely emitted from a methane-rich combustion source, located east of the observation site.&amp;#160;&lt;/p&gt;

scholarly journals Atmospheric Evolution of Molecular Weight Separated Brown Carbon from Biomass Burning

2018 ◽  
Author(s):  
Jenny P. S. Wong ◽  
Maria Tsagaraki ◽  
Irini Tsiodra ◽  
Nikolaos Mihalopoulos ◽  
Kalliopi Violaki ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Biomass Burning ◽  
Water Soluble ◽  
Brown Carbon ◽  
Atmospheric Lifetime ◽  
Radiative Balance ◽  
Considerable Uncertainty ◽  
Atmospheric Aging ◽  
Robust Model ◽  
The Stability

Abstract. Biomass burning is a major source of atmospheric brown carbon (BrC) and through its absorption of UV/VIS radiation, it can play an important role on the planetary radiative balance and atmospheric photochemistry. The considerable uncertainty of BrC impacts is associated with its poorly constrained sources, transformations and atmospheric lifetime. Here we report laboratory experiments that examined changes in the optical properties of the water-soluble BrC fraction of biomass burning particles. Effects of direct UVB photolysis and OH oxidation in the aqueous phase on molecular weight-separated BrC were studied. Results indicated that low molecular weight (MW) BrC ( 10 hours) biomass burning emissions, poor linear correlations were found between light absorptivity and levoglucosan, consistent with other studies suggesting a short atmospheric lifetime for levoglucosan. However, a much stronger correlation between light absorptivity and total hydrous sugars was observed, suggesting that they may serve as more robust tracers for aged biomass burning emissions. Overall, the results from this study suggest that robust model estimates of BrC radiative impacts require consideration of the atmospheric aging of BrC and the stability of high-MW BrC.

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