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Volume 18, issue 5 | Copyright
Atmos. Chem. Phys., 18, 3269-3287, 2018
https://doi.org/10.5194/acp-18-3269-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 07 Mar 2018

Research article | 07 Mar 2018

Organic functional groups in the submicron aerosol at 82.5° N, 62.5° W from 2012 to 2014

W. Richard Leaitch1, Lynn M. Russell2, Jun Liu2, Felicia Kolonjari1, Desiree Toom1, Lin Huang1, Sangeeta Sharma1, Alina Chivulescu1, Dan Veber1, and Wendy Zhang1 W. Richard Leaitch et al.
  • 1Environment and Climate Change Canada (ECCC), Toronto, ON, Canada
  • 2Scripps Institution of Oceanography, University of California, San Diego, CA, USA

Abstract. The first multi-year contributions from organic functional groups to the Arctic submicron aerosol are documented using 126 weekly-integrated samples collected from April 2012 to October 2014 at the Alert Observatory (82.45°N, 62.51°W). Results from the particle transport model FLEXPART, linear regressions among the organic and inorganic components and positive matrix factorization (PMF) enable associations of organic aerosol components with source types and regions. Lower organic mass (OM) concentrations but higher ratios of OM to non-sea-salt sulfate mass concentrations (nss-SO4=) accompany smaller particles during the summer (JJA). Conversely, higher OM but lower OMnss-SO4= accompany larger particles during winter–spring. OM ranges from 7 to 460ngm−3, and the study average is 129ngm−3. The monthly maximum in OM occurs during May, 1 month after the peak in nss-SO4= and 2 months after that of elemental carbon (EC). Winter (DJF), spring (MAM), summer and fall (SON) values of OMnss-SO4= are 26, 28, 107 and 39%, respectively, and overall about 40% of the weekly variability in the OM is associated with nss-SO4=. Respective study-averaged concentrations of alkane, alcohol, acid, amine and carbonyl groups are 57, 24, 23, 15 and 11ngm−3, representing 42, 22, 18, 14 and 5% of the OM, respectively. Carbonyl groups, detected mostly during spring, may have a connection with snow chemistry. The seasonally highest OC occurs during winter (0.85) and the lowest OC is during spring (0.51); increases in OC are largely due to increases in alcohol groups. During winter, more than 50% of the alcohol groups are associated with primary marine emissions, consistent with Shaw et al. (2010) and Frossard et al. (2011). A secondary marine connection, rather than a primary source, is suggested for the highest and most persistent OC observed during the coolest and cleanest summer (2013), when alcohol and acid groups made up 63% of the OM. A secondary marine source may be a general feature of the summer OM, but higher contributions from alkane groups to OM during the warmer summers of 2012 (53%) and 2014 (50%) were likely due to increased contributions from combustion sources. Evidence for significant contributions from biomass burning (BB) was present in 4% of the weeks. During the dark months (NDJF), 29, 28 and 14% of the nss-SO4=, EC and OM were associated with transport times over the gas flaring region of northern Russia and other parts of Eurasia. During spring, those percentages dropped to 11% for each of nss-SO4= and EC values, respectively, and there is no association of OM. Large percentages of the Arctic haze characterized at Alert likely have origins farther than 10 days of transport time and may be from outside of the Eurasian region. Possible sources of unusually high nss-SO4= and OM during September–October 2014 are volcanic emissions or the Smoking Hills' area of the Northwest Territories, Canada.

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Over 2 years of atmospheric aerosol organic functional group and microphysics measurements at the world's northernmost land observatory offer a unique high-latitude dataset. Lower organic mass (OM) concentrations and higher OM fractions accompany smaller particles during summer, with opposite results during winter to spring. Seasonally, the OM oxidation level is highest in winter, associated with primary marine alcohol groups. In summer, secondary processes dominate the marine influence on OM.
Over 2 years of atmospheric aerosol organic functional group and microphysics measurements at...
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