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Size distributions, sources and source areas of water-soluble organic carbon in urban background air

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TLDR
In this article, the results of one year long measurement period of the size distributions of water-soluble organic carbon (WSOC), inorganic ions and gravi- metric mass of particulate matter were presented.
Abstract
This paper represents the results of one year long measurement period of the size distributions of water- soluble organic carbon (WSOC), inorganic ions and gravi- metric mass of particulate matter. Measurements were done at an urban background station (SMEAR III) by using a micro-orifice uniform deposit impactor (MOUDI). The site is located in northern European boreal region in Helsinki, Finland. The WSOC size distribution measurements were completed with the chemical analysis of inorganic ions, or- ganic carbon (OC) and monosaccharide anhydrides from the filter samples (particle aerodynamic diameter smaller than 1µm, PM1). Gravimetric mass concentration varied during the MOUDI samplings between 3.4 and 55.0µg m 3 and the WSOC concentrations were between 0.3 and 7.4µg m 3 . On average, water-soluble particulate organic matter (WSPOM, WSOC multiplied by 1.6 to convert the analyzed carbon mass to organic matter mass) comprised 25±7.7% and 7.5±3.4% of aerosol PM1 mass and the PM1 10 mass, respectively. In- organic ions contributed 33±12% and 28±19% of the ana- lyzed PM1 and PM1 10 aerosol mass. Five different aerosol categories corresponding to differ- ent sources or source areas were identified (long-range trans- port aerosols, biomass burning aerosols from wild land fires and from small-scale wood combustion, aerosols originating from marine areas and from the clean arctic areas). Cat- egories were identified mainly using levoglucosan concen- tration level for wood combustion and air mass backward trajectories for other groups. Clear differences in WSOC concentrations and size distributions originating from differ- ent sources or source areas were observed, although there are also many other factors which might affect the results. E.g. the local conditions and sources of volatile organic com- pounds (VOCs) and aerosols as well as various transforma- tion processes are likely to have an impact on the measured aerosol composition. Using the source categories, it was identified that especially the oxidation products of biogenic VOCs in summer had a clear effect on WSOC concentra- tions.

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Journal ArticleDOI

Source apportionment of size-segregated atmospheric particles based on the major water-soluble components in Lecce (Italy).

TL;DR: In this work, aerosol samples were collected using a 10-stage Micro-Orifice Uniform Deposit Impactor and size-segregated source apportionment was performed using Positive Matrix Factorization (PMF), which was applied separately to the coarse and accumulation modes.
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Semi-continuous gas and inorganic aerosol measurements at a Finnish urban site: comparisons with filters, nitrogen in aerosol and gas phases, and aerosol acidity

TL;DR: In this paper, MARGA 2S was used to measure concentrations of 5 gases (HCl, HNO3, HONO, NH3, SO2) and 8 major inorganic ions in particles (Cl−, NO3−, SO42−, NH4+, Na+, K+, Mg2+, Ca2+) in two size ranges, Dp
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Chemical composition of fine particles in fresh smoke plumes from boreal wild-land fires in Europe.

TL;DR: Satellite observations employing MODIS sensor on board of NASA EOS Terra satellite with the dispersion model SILAM and the Fire Assimilation System were used for evaluation of the emission fluxes from wildfires and showed that the major growth in PM concentration was caused by submicrometer particles consisting mainly of particulate organic matter (POM).
Journal ArticleDOI

Comparison among filter-based, impactor-based and continuous techniques for measuring atmospheric fine sulfate and nitrate

TL;DR: In this article, a comparison of the performances of two filter-based samplers, including a honeycomb denuder filter-pack system, a Micro Orifice Uniform Deposit Impactor (MOUDI) and a real-time ambient ion monitor (AIM, URG9000B), was conducted at an urban site in Jinan, Shandong province, during the winter of 2007 and at a rural site near Beijing in the summer of 2008.
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Chemical Characterization of Water-Soluble Organic Aerosol in Contrasting Rural and Urban Environments in the Southeastern United States.

TL;DR: A novel system for direct and online characterization of water-solubility of organic aerosol (OA) by coupling a Particle Into Liquid Sampler (PILS) to a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) provides insights for interpretation of OA factors and improves understanding of the complex OA sources in the atmosphere.
References
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Journal ArticleDOI

Organic aerosol and global climate modelling: a review

TL;DR: In this article, the authors reviewed existing knowledge with regard to organic aerosol (OA) of importance for global climate modelling and defined critical gaps needed to reduce the involved uncertainties, and synthesized the information to provide a continuous analysis of the flow from the emitted material to the atmosphere up to the point of the climate impact of the produced organic aerosols.
Journal ArticleDOI

Species contributions to PM2.5 mass concentrations: Revisiting common assumptions for estimating organic mass

TL;DR: The authors revisited common assumptions for estimating PM2.5 mass concentration and found that these assumptions can be used to estimate organic mass in a wide range of scenarios, such as PM1.5.
Journal ArticleDOI

Organic atmospheric aerosols: Review and state of the science

TL;DR: In this article, the importance of organic aerosols in environmental issues is discussed, and a detailed overview of the major environmental issues known to be affected by organic aerosol is provided, followed by a description of the distribution, sources, and chemical and physical properties as they are currently understood.
Journal ArticleDOI

A Microorifice Uniform Deposit Impactor (MOUDI): Description, Calibration, and Use

TL;DR: In this paper, an eight-stage cascade impactor with cut sizes ranging from 0.056 to 18 μm at a flow rate of 30 L/min was developed, calibrated, and tested in field programs.
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