Atmospheric inorganic nitrogen input via dry, wet, and sea fog deposition to the subarctic western North Pacific Ocean

Aerosol, rainwater, and sea fog water samples were collected during the cruise conducted over the subarctic western North Pacific Ocean in the summer of 2008, in order to estimate dry, wet, and sea fog deposition fluxes of atmospheric inorganic nitrogen (N). During sea fog events, mean number densit...

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Main Authors: J. Jung, H. Furutani, M. Uematsu, S. Kim, S. Yoon
Format: Article
Language:English
Published: Copernicus Publications 2013-01-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/13/411/2013/acp-13-411-2013.pdf
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author J. Jung
H. Furutani
M. Uematsu
S. Kim
S. Yoon
author_facet J. Jung
H. Furutani
M. Uematsu
S. Kim
S. Yoon
author_sort J. Jung
collection DOAJ
description Aerosol, rainwater, and sea fog water samples were collected during the cruise conducted over the subarctic western North Pacific Ocean in the summer of 2008, in order to estimate dry, wet, and sea fog deposition fluxes of atmospheric inorganic nitrogen (N). During sea fog events, mean number densities of particles with diameters larger than 0.5 μm decreased by 12–78%, suggesting that particles with diameters larger than 0.5 μm could act preferentially as condensation nuclei (CN) for sea fog droplets. Mean concentrations of nitrate (NO<sub>3</sub><sup>−</sup>), methanesulfonic acid (MSA), and non sea-salt sulfate (nss-SO<sub>4</sub><sup>2−</sup>) in sea fog water were higher than those in rainwater, whereas those of ammonium (NH<sub>4</sub><sup>+</sup>) in both sea fog water and rainwater were similar. These results reveal that sea fog scavenged NO<sub>3</sub><sup>−</sup> and biogenic sulfur species more efficiently than rain. Mean dry, wet, and sea fog deposition fluxes for atmospheric total inorganic N (TIN; i.e. NH<sub>4</sub><sup>+</sup> + NO<sub>3</sub><sup>−</sup>) over the subarctic western North Pacific Ocean were estimated to be 4.9 μmol m<sup>−2</sup> d<sup>−1</sup>, 33 μmol m<sup>−2</sup> d<sup>−1</sup>, and 7.8 μmol m<sup>−2</sup> d<sup>−1</sup>, respectively. While NO<sub>3</sub><sup>−</sup> was the dominant inorganic N species in dry and sea fog deposition, inorganic N supplied to surface waters by wet deposition was predominantly by NH<sub>4</sub><sup>+</sup>. The contribution of dry, wet, and sea fog deposition to total deposition flux for TIN (46 μmol m<sup>−2</sup> d<sup>−1</sup>) were 11%, 72%, and 17%, respectively, suggesting that ignoring sea fog deposition would lead to underestimate of the total influx of atmospheric inorganic N into the subarctic western North Pacific Ocean, especially in summer periods.
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spelling doaj.art-a0e102bddacc4f4b830b3dcf29c02bb22022-12-22T00:57:27ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242013-01-0113141142810.5194/acp-13-411-2013Atmospheric inorganic nitrogen input via dry, wet, and sea fog deposition to the subarctic western North Pacific OceanJ. JungH. FurutaniM. UematsuS. KimS. YoonAerosol, rainwater, and sea fog water samples were collected during the cruise conducted over the subarctic western North Pacific Ocean in the summer of 2008, in order to estimate dry, wet, and sea fog deposition fluxes of atmospheric inorganic nitrogen (N). During sea fog events, mean number densities of particles with diameters larger than 0.5 μm decreased by 12–78%, suggesting that particles with diameters larger than 0.5 μm could act preferentially as condensation nuclei (CN) for sea fog droplets. Mean concentrations of nitrate (NO<sub>3</sub><sup>−</sup>), methanesulfonic acid (MSA), and non sea-salt sulfate (nss-SO<sub>4</sub><sup>2−</sup>) in sea fog water were higher than those in rainwater, whereas those of ammonium (NH<sub>4</sub><sup>+</sup>) in both sea fog water and rainwater were similar. These results reveal that sea fog scavenged NO<sub>3</sub><sup>−</sup> and biogenic sulfur species more efficiently than rain. Mean dry, wet, and sea fog deposition fluxes for atmospheric total inorganic N (TIN; i.e. NH<sub>4</sub><sup>+</sup> + NO<sub>3</sub><sup>−</sup>) over the subarctic western North Pacific Ocean were estimated to be 4.9 μmol m<sup>−2</sup> d<sup>−1</sup>, 33 μmol m<sup>−2</sup> d<sup>−1</sup>, and 7.8 μmol m<sup>−2</sup> d<sup>−1</sup>, respectively. While NO<sub>3</sub><sup>−</sup> was the dominant inorganic N species in dry and sea fog deposition, inorganic N supplied to surface waters by wet deposition was predominantly by NH<sub>4</sub><sup>+</sup>. The contribution of dry, wet, and sea fog deposition to total deposition flux for TIN (46 μmol m<sup>−2</sup> d<sup>−1</sup>) were 11%, 72%, and 17%, respectively, suggesting that ignoring sea fog deposition would lead to underestimate of the total influx of atmospheric inorganic N into the subarctic western North Pacific Ocean, especially in summer periods.http://www.atmos-chem-phys.net/13/411/2013/acp-13-411-2013.pdf
spellingShingle J. Jung
H. Furutani
M. Uematsu
S. Kim
S. Yoon
Atmospheric inorganic nitrogen input via dry, wet, and sea fog deposition to the subarctic western North Pacific Ocean
Atmospheric Chemistry and Physics
title Atmospheric inorganic nitrogen input via dry, wet, and sea fog deposition to the subarctic western North Pacific Ocean
title_full Atmospheric inorganic nitrogen input via dry, wet, and sea fog deposition to the subarctic western North Pacific Ocean
title_fullStr Atmospheric inorganic nitrogen input via dry, wet, and sea fog deposition to the subarctic western North Pacific Ocean
title_full_unstemmed Atmospheric inorganic nitrogen input via dry, wet, and sea fog deposition to the subarctic western North Pacific Ocean
title_short Atmospheric inorganic nitrogen input via dry, wet, and sea fog deposition to the subarctic western North Pacific Ocean
title_sort atmospheric inorganic nitrogen input via dry wet and sea fog deposition to the subarctic western north pacific ocean
url http://www.atmos-chem-phys.net/13/411/2013/acp-13-411-2013.pdf
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