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DOI10.5194/acp-18-6847-2018
Multi-model study of HTAP II on sulfur and nitrogen deposition
Tan, Jiani1; Fu, Joshua S.1; Dentener, Frank2; Sun, Jian1; Emmons, Louisa3; Tilmes, Simone3; Sudo, Kengo4; Flemming, Johannes5; Jonson, Jan Eiof6; Gravel, Sylvie7; Bian, Huisheng8; Davila, Yanko9; Henze, Daven K.9; Lund, Marianne T.10; Kucsera, Tom11; Takemura, Toshihiko12; Keating, Terry13
发表日期2018-05-16
ISSN1680-7316
卷号18期号:9页码:6847-6866
英文摘要

This study uses multi-model ensemble results of 11 models from the second phase of Task Force Hemispheric Transport of Air Pollution (HTAP II) to calculate the global sulfur (S) and nitrogen (N) deposition in 2010. Modeled wet deposition is evaluated with observation networks in North America, Europe and East Asia. The modeled results agree well with observations, with 76-83% of stations being predicted within +/- 50% of observations. The models underestimate SO42-, NO3- and NH4+ wet depositions in some European and East Asian stations but overestimate NO3- wet deposition in the eastern United States. Intercomparison with previous projects (PhotoComp, ACCMIP and HTAP I) shows that HTPA II has considerably improved the estimation of deposition at European and East Asian stations. Modeled dry deposition is generally higher than the "inferential" data calculated by observed concentration and modeled velocity in North America, but the inferential data have high uncertainty, too. The global S deposition is 84 Tg(S) in 2010, with 49% in continental regions and 51% in the ocean (19% of which coastal). The global N deposition consists of 59 Tg(N) oxi-dized nitrogen (NOy) deposition and 64 Tg(N) reduced nitrogen (NHx) deposition in 2010. About 65% of N is deposited in continental regions, and 35% in the ocean (15% of which coastal). The estimated outflow of pollution from land to ocean is about 4 Tg(S) for S deposition and 18 Tg(N) for N deposition. Comparing our results to the results in 2001 from HTAP I, we find that the global distributions of S and N deposition have changed considerably during the last 10 years. The global S deposition decreases 2 Tg(S) (3 %) from 2001 to 2010, with significant decreases in Europe (5 Tg(S) and 55 %), North America (3 Tg(S) and 29 %) and Russia (2 Tg(S) and 26 %), and increases in South Asia (2 Tg(S) and 42 %) and the Middle East (1 Tg(S) and 44 %). The global N deposition increases by 7 Tg(N) (6 %), mainly contributed by South Asia (5 Tg(N) and 39 %), East Asia (4 Tg(N) and 21 %) and Southeast Asia (2 Tg(N) and 21 %). The NHx deposition increases with no control policy on NH3 emission in North America. On the other hand, NOy deposition has started to dominate in East Asia (especially China) due to boosted NOx emission.


语种英语
WOS记录号WOS:000432392400004
来源期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
来源机构美国环保署
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/61949
作者单位1.Univ Tennessee, Dept Civil & Environm Engn, Knoxville, TN 37996 USA;
2.European Commiss, Inst Environm & Sustainabil Joint Res Ctr, Ispra, Italy;
3.Natl Ctr Atmospher Res, Atmospher Chem Observat & Modeling Lab, POB 3000, Boulder, CO 80307 USA;
4.Nagoya Univ, Chikusa Ku, Furo Cho, Nagoya, Aichi, Japan;
5.European Ctr Medium Range Weather Forecasts, Reading, Berks, England;
6.Norwegian Meteorol Inst, Oslo, Norway;
7.Meteorol Serv Canada, Meteorol Res Branch, Toronto, ON, Canada;
8.NASA, Goddard Space Flight Ctr, Greenbelt, MD USA;
9.Univ Colorado, Dept Mech Engn, Boulder, CO 80309 USA;
10.CICERO Ctr Int Climate Res, Oslo, Norway;
11.Univ Space Res Assoc, NASA GESTAR, Columbia, MD USA;
12.Kyushu Univ, Res Inst Appl Mech, Fukuoka, Japan;
13.US EPA, Washington, DC 20460 USA
推荐引用方式
GB/T 7714
Tan, Jiani,Fu, Joshua S.,Dentener, Frank,et al. Multi-model study of HTAP II on sulfur and nitrogen deposition[J]. 美国环保署,2018,18(9):6847-6866.
APA Tan, Jiani.,Fu, Joshua S..,Dentener, Frank.,Sun, Jian.,Emmons, Louisa.,...&Keating, Terry.(2018).Multi-model study of HTAP II on sulfur and nitrogen deposition.ATMOSPHERIC CHEMISTRY AND PHYSICS,18(9),6847-6866.
MLA Tan, Jiani,et al."Multi-model study of HTAP II on sulfur and nitrogen deposition".ATMOSPHERIC CHEMISTRY AND PHYSICS 18.9(2018):6847-6866.
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