Molecular and physical characteristics of aerosol at a remote free troposphere site: implications for atmospheric aging

Schum, Simeon K.; Zhang, Bo; Džepina, Katja; Fialho, Paulo; Mazzoleni, Claudio; Mazzoleni, Lynn R.

doi:10.5194/acp-18-14017-2018

Title: Molecular and physical characteristics of aerosol at a remote free troposphere site: implications for atmospheric aging

Journal Article · Tue Oct 02 00:00:00 EDT 2018 · Atmospheric Chemistry and Physics (Online)

DOI:https://doi.org/10.5194/acp-18-14017-2018· OSTI ID:1610911

Schum, Simeon K. ^[1];

^[2]; Džepina, Katja ^[3];

^[4];

^[5];

^[1]

Michigan Technological Univ., Houghton, MI (United States)
Michigan Technological Univ., Houghton, MI (United States); National Inst. of Aerospace, Hampton, VA (United States)
Michigan Technological Univ., Houghton, MI (United States); Univ. of Rijeka (Croatia)
Univ. of the Azores, Angra do Heroismo (Portugal)
Michigan Technological Univ., Houghton, MI (United States); Michigan Technological Univ., Houghton, MI (United States)

Aerosol properties are transformed by atmospheric processes during long-range transport and play a key role in the Earth's radiative balance. To understand the molecular and physical characteristics of free tropospheric aerosol, we studied samples collected at the Pico Mountain Observatory in the North Atlantic. The observatory is located in the marine free troposphere at 2225 m above sea level, on Pico Island in the Azores archipelago. The site is ideal for the study of long-range-transported free tropospheric aerosol with minimal local influence. Three aerosol samples with elevated organic carbon concentrations were selected for detailed analysis. FLEXPART retroplumes indicated that two of the samples were influenced by North American wildfire emissions transported in the free troposphere and one by North American outflow mainly transported within the marine boundary layer.Ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry was used to determine the detailed molecular composition of the samples. Thousands of molecular formulas were assigned to each of the individual samples. On average ~60 % of the molecular formulas contained only carbon, hydrogen, and oxygen atoms (CHO), ~30 %contained nitrogen (CHNO), and ~10 % contained sulfur (CHOS). The molecular formula compositions of the two wildfire-influenced aerosol samples transported mainly in the free troposphere had relatively low averageO/C ratios (0.48±0.13 and 0.45±0.11) despite the 7–10 days of transport time according to FLEXPART. In contrast, the molecular composition of the North American outflow transported mainly in the boundary layer had a higher average O/C ratio (0.57±0.17) with 3 days of transport time. To better understand the difference between free tropospheric transport and boundary layer transport, the meteorological conditions along the FLEXPART simulated transport pathways were extracted from the Global Forecast System analysis for the model grids. We used the extracted meteorological conditions and the observed molecular chemistry to predict the relative-humidity-dependent glass transition temperatures (T_g) of the aerosol components. Comparisons of the T_g to the ambient temperature indicated that a majority of the organic aerosol components transported in the free troposphere were more viscous and therefore less susceptible to oxidation than the organic aerosol components transported inthe boundary layer. Although the number of observations is limited, the results suggest that biomass burning organic aerosol injected into the free troposphere is more persistent than organic aerosol in the boundary layer having broader implications for aerosol aging.

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Research Organization:: Michigan Technological Univ., Houghton, MI (United States)

Sponsoring Organization:: USDOE Office of Science (SC); National Science Foundation (NSF)

Grant/Contract Number:: SC0006941; AGS-1110059

OSTI ID:: 1610911

Journal Information:: Atmospheric Chemistry and Physics (Online), Vol. 18, Issue 19; ISSN 1680-7324

Publisher:: European Geosciences UnionCopyright Statement

Country of Publication:: United States

Language:: English

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Cited by: 29 works

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