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DOI | 10.1029/2018GB005880 |
The Effect of Atmospheric Acid Processing on the Global Deposition of Bioavailable Phosphorus From Dust | |
Herbert R.J.; Krom M.D.; Carslaw K.S.; Stockdale A.; Mortimer R.J.G.; Benning L.G.; Pringle K.; Browse J. | |
发表日期 | 2018 |
ISSN | 0886-6236 |
EISSN | 1944-9224 |
起始页码 | 1367 |
结束页码 | 1385 |
卷号 | 32期号:9 |
英文摘要 | The role of dust as a source of bioavailable phosphorus (Bio-P) is quantified using a new parameterization for apatite dissolution in combination with global soil data maps and a global aerosol transport model. Mineral dust provides 31.2 Gg-P/year of Bio-P to the oceans, with 14.3 Gg-P/year from labile P present in the dust, and an additional 16.9 Gg-P/year from acid dissolution of apatite in the atmosphere, representing an increase of 120%. The North Atlantic, northwest Pacific, and Mediterranean Sea are identified as important sites of Bio-P deposition from mineral dust. The acid dissolution process increases the fraction of total-P that is bioavailable from ~10% globally from the labile pool to 18% in the Atlantic Ocean, 42% in the Pacific Ocean, and 20% in the Indian Ocean, with an ocean global mean value of 22%. Strong seasonal variations, especially in the North Pacific, northwest Atlantic, and Indian Ocean, are driven by large-scale meteorology and pollution sources from industrial and biomass-burning regions. Globally constant values of total-P content and bioavailable fraction used previously do not capture the simulated variability. We find particular sensitivity to the representation of particle-to-particle variability of apatite, which supplies Bio-P through acid-dissolution, and calcium carbonate, which helps to buffer the dissolution process. A modest 10% external mixing results in an increase of Bio-P deposition by 18%. The total Bio-P calculated here (31.2 Gg-P/year) represents a minimum compared to previous estimates due to the relatively low total-P in the global soil map used. ©2018. American Geophysical Union. All Rights Reserved. |
英文关键词 | acid processing; biogeochemistry; global modeling; mineral dust; oceans; phosphorus |
语种 | 英语 |
scopus关键词 | acid deposition; aerosol; atmosphere-ocean coupling; atmospheric deposition; bioavailability; biogeochemistry; buffering; calcium carbonate; dissolution; dust; environmental effect; phosphorus; source identification; Atlantic Ocean; Atlantic Ocean (North); Atlantic Ocean (Northwest); Mediterranean Sea; Mediterranean Sea (West); Pacific Ocean; Pacific Ocean (Northwest) |
来源期刊 | Global Biogeochemical Cycles
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/129795 |
作者单位 | School of Earth and Environment, University of Leeds, Leeds, United Kingdom; Now at Department of Meteorology, University of Reading, Reading, United Kingdom; Now at Morris Kahn Marine Research Station, Department of Marine Biology, Leon H. Charney School of Marine Science, University of Haifa, Haifa, Israel; School of Animal, Rural and Environmental Sciences, Nottingham Trent University, Nottinghamshire, United Kingdom; GFZ German Research Centre for Geosciences, Potsdam, Germany; Department of Earth Sciences, Free University of Berlin, Berlin, Germany; Now at College of Life and Environmental Sciences, University of Exeter, Penryn, United Kingdom |
推荐引用方式 GB/T 7714 | Herbert R.J.,Krom M.D.,Carslaw K.S.,et al. The Effect of Atmospheric Acid Processing on the Global Deposition of Bioavailable Phosphorus From Dust[J],2018,32(9). |
APA | Herbert R.J..,Krom M.D..,Carslaw K.S..,Stockdale A..,Mortimer R.J.G..,...&Browse J..(2018).The Effect of Atmospheric Acid Processing on the Global Deposition of Bioavailable Phosphorus From Dust.Global Biogeochemical Cycles,32(9). |
MLA | Herbert R.J.,et al."The Effect of Atmospheric Acid Processing on the Global Deposition of Bioavailable Phosphorus From Dust".Global Biogeochemical Cycles 32.9(2018). |
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