Atmospheric Reactive Nitrogen Deposition to the Global Ocean During the 2010s: Interannual Variation and Source Attribution

Abstract This study evaluates atmospheric reactive nitrogen deposition to the global ocean from 2010 to 2019 using the GEOS‐Chem model, quantifying the contributions of key anthropogenic and natural sources and examining the impacts of emissions and meteorological changes on interannual variations (IAVs). The average global oceanic nitrogen deposition is 40.7 Tg N yr −1 , with 78% deposited in the open ocean. Reduced nitrogen (NH x ) and oxidized nitrogen (NO y ) contribute equally predominantly through wet deposition (62%). Of the total nitrogen deposition to oceans, 39% originates from natural emissions, 33% from fuel combustion including shipping and aviation (11%), and 22% from agricultural activities. Transportation and agriculture are the major contributors in the Northern Hemispheric mid‐high latitude and Coastal biomes, whereas natural emissions are dominant in Trades and Southern Hemispheric biomes. Both wet and dry NO y deposition decreases in the Northern Hemisphere mid‐high latitudes but increases in tropical biomes, whereas NH x shows opposing changes in wet and dry deposition. Anthropogenic emissions drive over 60% of IAVs of oceanic nitrogen deposition except for the NH x deposition over tropical biomes. Changes in anthropogenic emissions from combustion sources not only influence NO y deposition through nitrogen oxides (NO x ) emissions from fuel combustions but also lead to opposing trends in wet and dry NH x deposition due to nonlinear chemistry of secondary inorganic aerosol formations. These findings highlight the need for integrated management strategies targeting multiple pollutants, including NO x , ammonia (NH 3 ), and sulfur dioxide (SO 2 ) along with international regulations on shipping and aviation to effectively control nitrogen deposition over the ocean.

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Publication Details

Journal
Journal of Geophysical Research Atmospheres
Published
2025-04-15
DOI
https://doi.org/10.1029/2024jd042789
Citations
4
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
5.20

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article

Atmospheric Reactive Nitrogen Deposition to the Global Ocean During the 2010s: Interannual Variation and Source Attribution

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4 citations
Journal of Geophysical Research Atmospheres
Atmospheric chemistry and aerosols
5.20
article

Atmospheric Reactive Nitrogen Deposition to the Global Ocean During the 2010s: Interannual Variation and Source Attribution

Yuanhong Zhao, Youfan Chen, Jingxu Wang, Shaofei Liu, Lin Zhang, Qiong Li, Yizhen Lin
article en
4 citations

Abstract

Abstract This study evaluates atmospheric reactive nitrogen deposition to the global ocean from 2010 to 2019 using the GEOS‐Chem model, quantifying the contributions of key anthropogenic and natural sources and examining the impacts of emissions and meteorological changes on interannual variations (IAVs). The average global oceanic nitrogen deposition is 40.7 Tg N yr −1 , with 78% deposited in the open ocean. Reduced nitrogen (NH x ) and oxidized nitrogen (NO y ) contribute equally predominantly through wet deposition (62%). Of the total nitrogen deposition to oceans, 39% originates from natural emissions, 33% from fuel combustion including shipping and aviation (11%), and 22% from agricultural activities. Transportation and agriculture are the major contributors in the Northern Hemispheric mid‐high latitude and Coastal biomes, whereas natural emissions are dominant in Trades and Southern Hemispheric biomes. Both wet and dry NO y deposition decreases in the Northern Hemisphere mid‐high latitudes but increases in tropical biomes, whereas NH x shows opposing changes in wet and dry deposition. Anthropogenic emissions drive over 60% of IAVs of oceanic nitrogen deposition except for the NH x deposition over tropical biomes. Changes in anthropogenic emissions from combustion sources not only influence NO y deposition through nitrogen oxides (NO x ) emissions from fuel combustions but also lead to opposing trends in wet and dry NH x deposition due to nonlinear chemistry of secondary inorganic aerosol formations. These findings highlight the need for integrated management strategies targeting multiple pollutants, including NO x , ammonia (NH 3 ), and sulfur dioxide (SO 2 ) along with international regulations on shipping and aviation to effectively control nitrogen deposition over the ocean.

Journal of Geophysical Research AtmospheresVol. 130(8)
Peking University (CN), Shandong Entry-Exit Inspection and Quarantine Bureau (CN), Sichuan Academy of Forestry (CN), Ocean University of China (CN)
Natural Science Foundation of Shandong Province
Openalex Percentile: Top 5%
Atmospheric chemistry and aerosols
5.20
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