TY - JOUR
T1 - Atmospheric particle abundance and sea salt aerosol observations in the springtime Arctic
T2 - A focus on blowing snow and leads
AU - Chen, Qianjie
AU - Mirrielees, Jessica A.
AU - Thanekar, Sham
AU - Loeb, Nicole A.
AU - Kirpes, Rachel M.
AU - Upchurch, Lucia M.
AU - Barget, Anna J.
AU - Lata, Nurun Nahar
AU - Raso, Angela R.W.
AU - McNamara, Stephen M.
AU - China, Swarup
AU - Quinn, Patricia K.
AU - Ault, Andrew P.
AU - Kennedy, Aaron
AU - Shepson, Paul B.
AU - Fuentes, Jose D.
AU - Pratt, Kerri A.
N1 - Funding Information:
This research has been supported by the National Science Foundation Office of Polar Programs (grant nos. 1417668, 1417906, 1417914, 2000493, 2000428, and 2000403), the National Aeronautics and Space Administration Earth Science Program (grant no. NNX14AP44G), DOE Atmospheric Systems Research program (grant no. DE-SC0019392), and a Sloan Research Fellowship to KAP. LMU was supported by the Cooperative Institute for Climate, Ocean, and Ecosystem Studies (CIOCES) under NOAA Cooperative Agreement NA20OAR4320271 (contribution no. 2022-1206). QC was supported by the Hong Kong General Research Fund (grant no. 15223221) for efforts during manuscript revisions.
Funding Information:
We thank the Ukpeaġvik Iñupiat Corporation – Science and Polar Field Services, as well as Dandan Wei and Jesus Ruiz-Plancarte from Pennsylvania State University, for logistical support during this field campaign. We thank NOAA Barrow Observatory for CPC aerosol number concentration data and DOE ARM Observatory for ceilometer data. CCSEM-EDX analyses were performed at the Environmental Molecular Sciences Laboratory (EMSL), a national scientific user facility located at the Pacific Northwest National Laboratory (PNNL) and sponsored by the Office of Biological and Environmental Research of the US DOE. PNNL is operated for the DOE by Battelle Memorial Institute under contract no. DE-AC06-76RL0 1830. PKQ acknowledges PMEL contribution number 5174.
Publisher Copyright:
© Copyright:
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Sea salt aerosols play an important role in the radiation budget and atmospheric composition over the Arctic, where the climate is rapidly changing. Previous observational studies have shown that Arctic sea ice leads are an important source of sea salt aerosols, and modeling efforts have also proposed blowing snow sublimation as a source. In this study, size-resolved atmospheric particle number concentrations and chemical composition were measured at the Arctic coastal tundra site of Utqiaavik, Alaska, during spring (3 April-7 May 2016). Blowing snow conditions were observed during 25g% of the 5-week study period and were overpredicted by a commonly used blowing snow parameterization based solely on wind speed and temperature. Throughout the study, open leads were present locally. During periods when blowing snow was observed, significant increases in the number concentrations of 0.01-0.06gμm particles (factor of 6, on average) and 0.06-0.3gμm particles (67g%, on average) and a significant decrease (82g%, on average) in 1-4gμm particles were observed compared to low wind speed periods. These size distribution changes were likely caused by the generation of ultrafine particles from leads and/or blowing snow, with scavenging of supermicron particles by blowing snow. At elevated wind speeds, both submicron and supermicron sodium and chloride mass concentrations were enhanced, consistent with wind-dependent local sea salt aerosol production. At moderate wind speeds below the threshold for blowing snow as well as during observed blowing snow, individual sea spray aerosol particles were measured. These individual salt particles were enriched in calcium relative to sodium in seawater due to the binding of this divalent cation with organic matter in the sea surface microlayer and subsequent enrichment during seawater bubble bursting. The chemical composition of the surface snowpack also showed contributions from sea spray aerosol deposition. Overall, these results show the contribution of sea spray aerosol production from leads on both aerosols and the surface snowpack. Therefore, if blowing snow sublimation contributed to the observed sea salt aerosol, the snow being sublimated would have been impacted by sea spray aerosol deposition rather than upward brine migration through the snowpack. Sea spray aerosol production from leads is expected to increase, with thinning and fracturing of sea ice in the rapidly warming Arctic.
AB - Sea salt aerosols play an important role in the radiation budget and atmospheric composition over the Arctic, where the climate is rapidly changing. Previous observational studies have shown that Arctic sea ice leads are an important source of sea salt aerosols, and modeling efforts have also proposed blowing snow sublimation as a source. In this study, size-resolved atmospheric particle number concentrations and chemical composition were measured at the Arctic coastal tundra site of Utqiaavik, Alaska, during spring (3 April-7 May 2016). Blowing snow conditions were observed during 25g% of the 5-week study period and were overpredicted by a commonly used blowing snow parameterization based solely on wind speed and temperature. Throughout the study, open leads were present locally. During periods when blowing snow was observed, significant increases in the number concentrations of 0.01-0.06gμm particles (factor of 6, on average) and 0.06-0.3gμm particles (67g%, on average) and a significant decrease (82g%, on average) in 1-4gμm particles were observed compared to low wind speed periods. These size distribution changes were likely caused by the generation of ultrafine particles from leads and/or blowing snow, with scavenging of supermicron particles by blowing snow. At elevated wind speeds, both submicron and supermicron sodium and chloride mass concentrations were enhanced, consistent with wind-dependent local sea salt aerosol production. At moderate wind speeds below the threshold for blowing snow as well as during observed blowing snow, individual sea spray aerosol particles were measured. These individual salt particles were enriched in calcium relative to sodium in seawater due to the binding of this divalent cation with organic matter in the sea surface microlayer and subsequent enrichment during seawater bubble bursting. The chemical composition of the surface snowpack also showed contributions from sea spray aerosol deposition. Overall, these results show the contribution of sea spray aerosol production from leads on both aerosols and the surface snowpack. Therefore, if blowing snow sublimation contributed to the observed sea salt aerosol, the snow being sublimated would have been impacted by sea spray aerosol deposition rather than upward brine migration through the snowpack. Sea spray aerosol production from leads is expected to increase, with thinning and fracturing of sea ice in the rapidly warming Arctic.
UR - http://www.scopus.com/inward/record.url?scp=85144380083&partnerID=8YFLogxK
U2 - 10.5194/acp-22-15263-2022
DO - 10.5194/acp-22-15263-2022
M3 - Journal article
AN - SCOPUS:85144380083
SN - 1680-7316
VL - 22
SP - 15263
EP - 15285
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 23
ER -