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Black carbon (BC), brown carbon, and light‐absorbing iron oxides (FeOx) aerosols affect Earth's energy budget through their strong absorption of solar radiation. FeOx aerosols can also affect global biogeochemical cycles through their role as a nutrient for oceanic phytoplankton. However, observational data for these aerosols required for evaluating their effects using global models are scarce, especially for FeOx. Here, we summarize and compare the data sets of BC and FeOx from five ground‐based and three aircraft observation campaigns conducted in the East Asian and Arctic regions during the 2009–2018 period acquired using a modified single‐particle soot photometer. In these campaigns, >80% of FeOx‐containing aerosols in the 170–270 nm FeOx core size range had microphysical features indicating an anthropogenic origin. The particle size distribution for each of the BC and FeOx was similar in all of the data sets except for those dominated by fresh urban pollution or pristine Arctic air. The campaign‐averaged mass concentrations of FeOx and BC were ~60–360 ng/m3 and ~240–1,300 ng/m3, respectively, in East Asia, and ~6 ng/m3 and ~20–30 ng/m3, respectively, in the Arctic. The campaign‐averaged FeOx/BC mass concentration ratio varied within a narrow range of 0.2–0.6 in both East Asian and Arctic regions. In every campaign, FeOx, BC, and carbon monoxide were tightly correlated with each other with similar slope to the urban campaigns (around Tokyo), implying the spatiotemporal variation of anthropogenic FeOx emission around northern middle‐to‐high latitudes is similar to those of anthropogenic BC and CO emissions. Key Points: Mass concentrations of anthropogenic iron oxide (FeOx) were at least 20% of those of black carbon (BC) in both East Asia and the ArcticFeOx, BC, and carbon monoxide were tightly correlated with each other in both East Asia and the ArcticParticle size distributions of both FeOx and BC were presented and compared in detail [ABSTRACT FROM AUTHOR]

Long-term measurements of black carbon (BC) aerosols by filter-based absorption photometers with a heated inlet (COSMOS) in different regions have been useful in elucidating spatial variations and radiative impacts of BC. Evaluations of mass concentrations of BC (MBC) measured by the COSMOS have been made by our previous studies through comparisons with other measurement techniques. However, how variations in the microphysical properties of BC and the co-existing light scattering aerosols affect the COSMOS measurements should be evaluated in more detail. In this study, we assessed these potential effects under various field environments in the Arctic and in the East Asia. From the slopes of the correlation plots between the MBC values measured by the COSMOS and a single-particle soot photometer, the average accuracy of the COSMOS was estimated as ∼10% in the MBC range 1–3000 ng m−3. On an hourly basis, the estimated sensitivity of the COSMOS MBC values to the changes in the BC size distributions was less than 10%, within the typical variabilities of BC size at individual observation sites. The COSMOS measurements depended little on the mixing states of BC and the concentrations of co-existing light scattering aerosols, except in the maritime air masses of East Asia, where the relative abundance of sea salt to BC was very high. The MBC measured by COSMOS also well agreed with elemental carbon measurements. Our results demonstrate the high reliability of COSMOS measurements under various environments. Copyright © 2019 American Association for Aerosol Research [ABSTRACT FROM AUTHOR]