TY - JOUR
T1 - Multi-model study of HTAP II on sulfur and nitrogen deposition
AU - Tan, Jiani
AU - Fu, Joshua S.
AU - Dentener, Frank
AU - Sun, Jian
AU - Emmons, Louisa
AU - Tilmes, Simone
AU - Sudo, Kengo
AU - Flemming, Johannes
AU - Jonson, Jan Eiof
AU - Gravel, Sylvie
AU - Bian, Huisheng
AU - Davila, Yanko
AU - Henze, Daven K.
AU - Lund, Marianne T.
AU - Kucsera, Tom
AU - Takemura, Toshihiko
AU - Keating, Terry
N1 - Funding Information:
Acknowledgements. We thank all participating modeling groups in HTAP II for providing the simulation data. We thank Robert Vet for providing the multi-model ensemble results of HTAP I. The National Center for Atmospheric Research is sponsored by the National Science Foundation. The CESM project is supported by the National Science Foundation and the Office of Science (BER) of the US Department of Energy. Computing resources were provided by the Climate Simulation Laboratory at NCAR’s Computational and Information Systems Laboratory (CISL), sponsored by the National Science Foundation and other agencies. We acknowledge the support by NASA HAQAST (grant no. NNX16AQ19G). We also acknowledge the support by the supercomputer system of the National Institute for Environmental Studies, Japan, and the Environment Research and Technology Development Fund (S-12-3) of the Ministry of the Environment, Japan, JSPS KAKENHI (grant no. 5H01728).
Publisher Copyright:
© 2018 Author(s).
PY - 2018/5/16
Y1 - 2018/5/16
N2 - 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 q inferential/q data calculated by observed concentration and modeled velocity in North America, but the inferential data have high uncertainty, too. The global S deposition is 84Tg(S) in 2010, with 49% in continental regions and 51% in the ocean (19% of which coastal). The global N deposition consists of 59Tg(N) oxidized nitrogen (NOy) deposition and 64Tg(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 4Tg(S) for S deposition and 18Tg(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 2Tg(S) (3%) from 2001 to 2010, with significant decreases in Europe (5Tg(S) and 55%), North America (3Tg(S) and 29%) and Russia (2Tg(S) and 26%), and increases in South Asia (2Tg(S) and 42%) and the Middle East (1Tg(S) and 44%). The global N deposition increases by 7Tg(N) (6%), mainly contributed by South Asia (5Tg(N) and 39%), East Asia (4Tg(N) and 21%) and Southeast Asia (2Tg(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.
AB - 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 q inferential/q data calculated by observed concentration and modeled velocity in North America, but the inferential data have high uncertainty, too. The global S deposition is 84Tg(S) in 2010, with 49% in continental regions and 51% in the ocean (19% of which coastal). The global N deposition consists of 59Tg(N) oxidized nitrogen (NOy) deposition and 64Tg(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 4Tg(S) for S deposition and 18Tg(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 2Tg(S) (3%) from 2001 to 2010, with significant decreases in Europe (5Tg(S) and 55%), North America (3Tg(S) and 29%) and Russia (2Tg(S) and 26%), and increases in South Asia (2Tg(S) and 42%) and the Middle East (1Tg(S) and 44%). The global N deposition increases by 7Tg(N) (6%), mainly contributed by South Asia (5Tg(N) and 39%), East Asia (4Tg(N) and 21%) and Southeast Asia (2Tg(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.
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U2 - 10.5194/acp-18-6847-2018
DO - 10.5194/acp-18-6847-2018
M3 - Article
AN - SCOPUS:85047426850
SN - 1680-7316
VL - 18
SP - 6847
EP - 6866
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 9
ER -