4.7 Article

Sources of reactive nitrogen in marine aerosol over the Northwest Pacific Ocean in spring

Journal

ATMOSPHERIC CHEMISTRY AND PHYSICS
Volume 18, Issue 9, Pages 6207-6222

Publisher

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-18-6207-2018

Keywords

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Funding

  1. National Natural Science Foundation of China [NSFC U1305233, NSFC 41763001]
  2. Major State Basic Research Development Program of China (973 program) [2014CB953702, 2015CB954003]
  3. National Natural Science Foundation Committee and Hong Kong Research Grants Council Joint Foundation [NSFC-RGC 41561164019]
  4. Doctoral Scientific Research Foundation of East China University of Technology [DHBK2016105]
  5. Science and technology project of the Jiangxi Provincial Department of Education [GJJ160580]
  6. Scientific Research Foundation of the East China University of Technology for the Science and Technology Innovation Team [DHKT2015101]

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Atmospheric deposition of long-range transport of anthropogenic reactive nitrogen (N-r, mainly comprised of NHx, NOy and water-soluble organic nitrogen, WSON) from continents may have profound impact on marine biogeochemistry. In addition, surface ocean dissolved organic nitrogen (DON) may also contribute to aerosol WSON in the overlying atmosphere. Despite the importance of off-continent dispersion and N-r interactions at the atmosphere-ocean boundary, our knowledge of the sources of various nitrogen species in the atmosphere over the open ocean remains limited due to insufficient observations. We conducted two cruises in the spring of 2014 and 2015 from the coast of China through the East China seas (ECSs, i.e. the Yellow Sea and East China Sea) to the open ocean (i.e. the Northwest Pacific Ocean, NWPO). Concentrations of water-soluble total nitrogen (WSTN), NO3- and NH4+, as well as the delta N-15 of WSTN and NO3- in marine aerosol, were measured during both cruises. In the spring of 2015, we also analysed the concentrations and delta N-15 of NO3- and the DON of surface seawater (SSW; at a depth of 5 m) along the cruise track. Aerosol NO3-, NH4+ and WSON decreased logarithmically (1-2 orders of magnitude) with distance from the shore, reflecting strong anthropogenic emission sources of NO3-, NH4+ and WSON in China. Average aerosol NO3- and NH4- concentrations were significantly higher in 2014 (even in the remote NWOP) than in 2015 due to the stronger wind field in 2014, underscoring the role of the Asian winter monsoon in the seaward transport of anthropogenic NO3- and NH4+. However, the background aerosol WSON over the NWPO in 2015 (13.3 +/- 8.5 nmol m(-3)) was similar to that in 2014 (12.2 +/- 6.3 nmol m(-3)), suggesting an additional non-anthropogenic WSON source in the open ocean. Obviously, marine DON emissions should be considered in model and field assessments of net atmospheric WSON deposition in the open ocean. This study contributes information on parallel isotopic marine DON composition and aerosol N-r datasets, but more research is required to explore complex N-r sources and deposition processes in order to advance our understanding of anthropogenic influences on the marine nitrogen cycle and nitrogen exchange at land-ocean and atmosphere-ocean interfaces.

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