Wildfire is one of the main sources of PM (particulate matter with aerodynamic diameter < 2.5 μm) in the Alaskan summer. The complexity in wildfire smokes, as well as limited coverage of ground measurements, poses a big challenge to estimate surface PM during wildfire season in Alaska. Here we aim at proposing a quick and direct method to estimate surface PM over Alaska, especially in places exposed to strong wildfire events with limited measurements. We compare the AOD-surface PM conversion factor (η = PM/AOD; AOD, aerosol optical depth) from the chemical transport model GEOS-Chem (η) and from observations (η). We show that η is biased high compared to η under smoky conditions, largely because GEOS-Chem assigns the majority of AOD (67%) within the planetary boundary layer (PBL) when AOD > 1, inconsistent with satellite retrievals from CALIOP. The overestimation in η can be to some extent improved by increasing the injection height of wildfire emissions. We constructed a piecewise function for η across different AOD ranges based on VIIRS-SNPP AOD and PurpleAir surface PM measurements over Alaska in the 2019 summer and then applied it on VIIRS AOD to derive daily surface PM over continental Alaska in the 2021 and 2022 summers. The derived satellite PM shows a good agreement with corrected PurpleAir PM in Alaska during the 2021 and 2022 summers, suggesting that aerosol vertical distribution likely represents the largest uncertainty in converting AOD to surface PM concentrations. This piecewise function, η', shows the capability of providing an observation-based, quick and direct estimation of daily surface PM over the whole of Alaska during wildfires, without running a 3-D model in real time.
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http://dx.doi.org/10.1021/acsestair.4c00120 | DOI Listing |
ACS Earth Space Chem
December 2024
Department of Chemistry and Biochemistry, University of California San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States.
As wildfire events become more frequent, there is a need to better understand the impact of smoke on the environment and human health. Smoke, or biomass burning aerosol (BBA), can undergo atmospheric processing changing its chemical and optical properties. We examined the interactions between four lignin pyrolysis products (catechol, syringol, syringic acid, and vanillic acid) and three BBA-relevant iron oxide mineral phases (hematite, maghemite, and magnetite) using attenuated total reflectance-Fourier transform infrared spectroscopy and dissolved iron measurements to better understand how atmospheric processing changes concentrations of soluble iron, iron oxidation state, and brown carbon abundance.
View Article and Find Full Text PDFPhotochem Photobiol Sci
December 2024
Institute of Meteorology and Climate Research Atmospheric Trace Gases and Remote Sensing, Karlsruhe Institute of Technology, Karlsruhe, Germany.
This paper investigates the evolution of changes in surface ultraviolet (UV) radiation globally, emphasizing the significant impacts of key factors influencing its variability, i.e., total column ozone, aerosols, clouds, and surface reflectivity.
View Article and Find Full Text PDFCryst Growth Des
December 2024
Materials Chemistry Center, Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ, U.K.
Mo-doped ZnO (MZO), F-doped ZnO (FZO), and Mo/F-codoped ZnO (MFZO) films have been deposited using a simple, cheap, and effective thin-film preparation route, aerosol-assisted chemical vapor deposition (AACVD). ZnO was successfully doped with Mo and/or F, confirmed by X-ray photoelectron spectroscopy (XPS) and by a decrease in unit cell parameters from X-ray diffraction (XRD). XRD also confirmed that all of the films had hexagonal wurtzite ZnO structures.
View Article and Find Full Text PDFSci Total Environ
December 2024
Department of Public Health Sciences, University of Rochester, School of Medicine and Dentistry, Rochester, NY, USA; Institute for a Sustainable Environment, Clarkson University, Potsdam, NY, USA.
Advanced receptor models can leverage the information derived from optical and chemical variables as input by a variety of instruments at different time resolutions to extract the source specific absorption Ångström exponent (AAE) from aerosol absorption. The multilinear engine (ME-2), a Positive Matrix Factorization (PMF) solver, serves as a proficient tool for performing such analyses, thereby overcoming the constraints imposed by the assumptions in current optical source apportionment methods such as the Aethalometer approach since the use of a-priori AAE values introduces additional uncertainty into the results of optical methods. Comprehensive PM chemical speciation datasets, and aerosol absorption coefficients (b, λ) at seven wavelengths measured by an Aethalometer (AE33), were used in multi-time source apportionment (MT-PMF).
View Article and Find Full Text PDFSci Total Environ
December 2024
Qingdao Key Laboratory for Prevention and Control of Atmospheric Pollution in Coastal Cities, Environment Research Institute, Shandong University, Qingdao 266237, China. Electronic address:
Marine aerosols are major components of atmospheric aerosols, playing substantial roles in influencing the regional and global environment and climate. Marine aerosols are not only produced by seawater directly, but also by indirect processes such as atmospheric oxidation of marine bioactive gases as well as terrestrial transport. Over the Eastern China Marginal Seas (ECMS), marine aerosols are strongly affected by marine emission and transport of terrestrial aerosols.
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