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« Previous Abstract"Identifying the wintertime sources of volatile organic compounds (VOCs) from MAX-DOAS measured formaldehyde and glyoxal in Chongqing, southwest China"    Next AbstractDevelopment and application of observable response indicators for design of an effective ozone and fine particle pollution control strategy in China »

Atmos Chem Phys


Title:Impacts of aerosol direct effects on tropospheric ozone through changes in atmospheric dynamics and photolysis rates
Author(s):Xing J; Wang J; Mathur R; Wang S; Sarwar G; Pleim J; Hogrefe C; Zhang Y; Jiang J; Wong DC; Hao J;
Address:"State Key Joint Laboratory of Environmental Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, China. The U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA"
Journal Title:Atmos Chem Phys
Year:2017
Volume:17
Issue:16
Page Number:9869 - 9883
DOI: 10.5194/acp-17-9869-2017
ISSN/ISBN:1680-7316 (Print) 1680-7324 (Electronic) 1680-7316 (Linking)
Abstract:"Aerosol direct effects (ADEs), i.e., scattering and absorption of incoming solar radiation, reduce radiation reaching the ground and the resultant photolysis attenuation can decrease ozone (O(3)) formation in polluted areas. One the other hand, evidence also suggests that ADE-associated cooling suppresses atmospheric ventilation, thereby enhancing surface-level O(3). Assessment of ADE impacts is thus important for understanding emission reduction strategies that seek co-benefits associated with reductions in both particuate matter and O(3) levels. This study quantifies the impacts of ADEs on tropospheric ozone by using a two-way online coupled meteorology and atmospheric chemistry model, WRF- CMAQ, using a process analysis methodology. Two mani-festations of ADE impacts on O3 including changes in atmospheric dynamics (»+GDynamics) and changes in photolysis rates (?OsPhotolysis) were assessed separately through multiple scenario simulations for January and July of 2013 over China. Results suggest that ADEs reduced surface daily maxima 1 h O(3) (DM1O(3)) in China by up to 39mugm(-3) through the combination of ?OsDynamics and ?OsPhotolysis in January but enhanced surface DM1O(3) by up to 4mugm(-3) in July. Increased O(3) in July is largely attributed to ?OsDynamics, which causes a weaker O(3) sink of dry deposition and a stronger O(3) source of photochemistry due to the stabilization of the at-mosphere. Meanwhile, surface OH is also enhanced at noon in July, though its daytime average values are reduced in January. An increased OH chain length and a shift towards more volatile organic compound (VOC)-limited conditions are found due to ADEs in both January and July. This study suggests that reducing ADEs may have the potential risk of increasing O(3) in winter, but it will benefit the reduction in maxima O(3) in summer"
Keywords:
Notes:"PubMed-not-MEDLINEXing, Jia Wang, Jiandong Mathur, Rohit Wang, Shuxiao Sarwar, Golam Pleim, Jonathan Hogrefe, Christian Zhang, Yuqiang Jiang, Jingkun Wong, David C Hao, Jiming eng EPA999999/Intramural EPA/ Germany 2017/01/01 Atmos Chem Phys. 2017; 17(16):9869-9883. doi: 10.5194/acp-17-9869-2017"

 
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