Altieri Katye E, Fawcett Sarah E, Peters Andrew J, Sigman Daniel M, Hastings Meredith G
Energy Research Centre, University of Cape Town, Cape Town 7701, South Africa;
Department of Geosciences, Princeton University, Princeton, NJ 08544; Department of Oceanography, University of Cape Town, Cape Town 7701, South Africa;
Proc Natl Acad Sci U S A. 2016 Jan 26;113(4):925-30. doi: 10.1073/pnas.1516847113. Epub 2016 Jan 6.
Global models estimate that the anthropogenic component of atmospheric nitrogen (N) deposition to the ocean accounts for up to a third of the ocean's external N supply and 10% of anthropogenic CO2 uptake. However, there are few observational constraints from the marine atmospheric environment to validate these findings. Due to the paucity of atmospheric organic N data, the largest uncertainties related to atmospheric N deposition are the sources and cycling of organic N, which is 20-80% of total N deposition. We studied the concentration and chemical composition of rainwater and aerosol organic N collected on the island of Bermuda in the western North Atlantic Ocean over 18 mo. Here, we show that the water-soluble organic N concentration ([WSON]) in marine aerosol is strongly correlated with surface ocean primary productivity and wind speed, suggesting a marine biogenic source for aerosol WSON. The chemical composition of high-[WSON] aerosols also indicates a primary marine source. We find that the WSON in marine rain is compositionally different from that in concurrently collected aerosols, suggesting that in-cloud scavenging (as opposed to below-cloud "washout") is the main contributor to rain WSON. We conclude that anthropogenic activity is not a significant source of organic N to the marine atmosphere over the North Atlantic, despite downwind transport from large pollution sources in North America. This, in conjunction with previous work on ammonium and nitrate, leads to the conclusion that only 27% of total N deposition to the global ocean is anthropogenic, in contrast to the 80% estimated previously.
全球模型估计,海洋大气氮(N)沉降的人为成分占海洋外部氮供应的三分之一,占人为二氧化碳吸收量的10%。然而,海洋大气环境的观测约束很少,无法验证这些发现。由于大气有机氮数据匮乏,与大气氮沉降相关的最大不确定性在于有机氮的来源和循环,有机氮占总氮沉降的20%-80%。我们研究了北大西洋西部百慕大群岛18个月内收集的雨水和气溶胶有机氮的浓度和化学成分。在此,我们表明海洋气溶胶中的水溶性有机氮浓度([WSON])与表层海洋初级生产力和风速密切相关,这表明气溶胶WSON有海洋生物源。高[WSON]气溶胶的化学成分也表明其主要来源于海洋。我们发现海洋降雨中的WSON在成分上与同时收集的气溶胶中的不同,这表明云内清除(与云下“冲刷”相对)是降雨WSON的主要来源。我们得出结论,尽管有来自北美大型污染源的顺风输送,但人为活动并非北大西洋海洋大气中有机氮的重要来源。结合之前关于铵和硝酸盐的研究,得出的结论是,全球海洋总氮沉降中只有27%是人为造成的,而之前的估计为80%。