Global S&T Development Trend Analysis Platform of Resources and Environment
DOI | 10.5194/acp-19-15691-2019 |
Wintertime spatial distribution of ammonia and its emission sources in the Great Salt Lake region | |
Moravek, Alexander1,8; Murphy, Jennifer G.1; Hrdina, Amy1,9; Lin, John C.2; Pennell, Christopher3; Franchin, Alessandro4,5; Middlebrook, Ann M.5; Fibiger, Dorothy L.4,5,10; Womack, Caroline C.4,5; McDuffie, Erin E.4,5,6,11; Martin, Randal7; Moore, Kori7,12; Baasandorj, Munkhbayar2,3; Brown, Steven S.5,6 | |
2019-12-20 | |
发表期刊 | ATMOSPHERIC CHEMISTRY AND PHYSICS
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ISSN | 1680-7316 |
EISSN | 1680-7324 |
出版年 | 2019 |
卷号 | 19期号:24页码:15691-15709 |
文章类型 | Article |
语种 | 英语 |
国家 | Canada; USA |
英文摘要 | Ammonium-containing aerosols are a major component of wintertime air pollution in many densely populated regions around the world. Especially in mountain basins, the formation of persistent cold-air pools (PCAPs) can enhance particulate matter with diameters less than 2.5 mu m (PM2.5) to levels above air quality standards. Under these conditions, PM2.5 in the Great Salt Lake region of northern Utah has been shown to be primarily composed of ammonium nitrate; however, its formation processes and sources of its precursors are not fully understood. Hence, it is key to understanding the emission sources of its gas phase precursor, ammonia (NH3). To investigate the formation of ammonium nitrate, a suite of trace gases and aerosol composition were sampled from the NOAA Twin Otter aircraft during the Utah Winter Fine Particulate Study (UWFPS) in January and February 2017. NH3 was measured using a quantum cascade tunable infrared laser differential absorption spectrometer (QC-TILDAS), while aerosol composition, including particulate ammonium (pNH(4)), was measured with an aerosol mass spectrometer (AMS). The origin of the sampled air masses was investigated using the Stochastic TimeInverted Lagrangian Transport (STILT) model and combined with an NH3 emission inventory to obtain model-predicted NHx (= NH3 pNH(4)) enhancements. Enhancements represent the increase in NH3 mixing ratios within the last 24 h due to emissions within the model footprint. Comparison of these NIL, enhancements with measured NIL, from the Twin Otter shows that modelled values are a factor of 1.6 to 4.4 lower for the three major valleys in the region. Among these, the underestimation is largest for Cache Valley, an area with intensive agricultural activities. We find that one explanation for the underestimation of wintertime emissions may be the seasonality factors applied to NH3 emissions from livestock. An investigation of inter-valley exchange revealed that transport of NH3 between major valleys was limited and PM2.5 in Salt Lake Valley (the most densely populated area in Utah) was not significantly impacted by NH3 from the agricultural areas in Cache Valley. We found that in Salt Lake Valley around two thirds of NHx originated within the valley, while about 30 % originated from mobile sources and 60 % from area source emissions in the region. For Cache Valley, a large fraction of NOx potentially leading to PM2.5 formation may not be locally emitted but mixed in from other counties. |
领域 | 地球科学 |
收录类别 | SCI-E |
WOS记录号 | WOS:000504010900006 |
WOS关键词 | AEROSOL MASS-SPECTROMETER ; FINE-PARTICULATE MATTER ; REACTIVE NITROGEN ; UNITED-STATES ; QC-TILDAS ; POLLUTION ; AIRBORNE ; NITRATE ; MODEL ; NH3 |
WOS类目 | Environmental Sciences ; Meteorology & Atmospheric Sciences |
WOS研究方向 | Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://119.78.100.173/C666/handle/2XK7JSWQ/224156 |
专题 | 环境与发展全球科技态势 |
作者单位 | 1.Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada; 2.Univ Utah, Dept Atmospher Sci, Salt Lake City, UT 84112 USA; 3.Utah Dept Environm Qual, Div Air Qual, Salt Lake City, UT 84114 USA; 4.Univ Colorado, CIRES, Boulder, CO 80309 USA; 5.NOAA, Chem Sci Div, ESRL, Boulder, CO 80305 USA; 6.Univ Colorado, Dept Chem, Boulder, CO 80309 USA; 7.Utah State Univ, Dept Civil & Environm Engn, Logan, UT 84322 USA; 8.York Univ, Dept Chem, Toronto, ON M3J 1P3, Canada; 9.MIT, Dept Civil & Environm Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA; 10.Calif Air Resources Board, Sacramento, CA 95814 USA; 11.Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B2H 4R2, Canada; 12.Space Dynam Lab, Logan, UT 84341 USA |
推荐引用方式 GB/T 7714 | Moravek, Alexander,Murphy, Jennifer G.,Hrdina, Amy,et al. Wintertime spatial distribution of ammonia and its emission sources in the Great Salt Lake region[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2019,19(24):15691-15709. |
APA | Moravek, Alexander.,Murphy, Jennifer G..,Hrdina, Amy.,Lin, John C..,Pennell, Christopher.,...&Brown, Steven S..(2019).Wintertime spatial distribution of ammonia and its emission sources in the Great Salt Lake region.ATMOSPHERIC CHEMISTRY AND PHYSICS,19(24),15691-15709. |
MLA | Moravek, Alexander,et al."Wintertime spatial distribution of ammonia and its emission sources in the Great Salt Lake region".ATMOSPHERIC CHEMISTRY AND PHYSICS 19.24(2019):15691-15709. |
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