GSTDTAP  > 地球科学
DOI10.5194/acp-17-10071-2017
Global deposition of total reactive nitrogen oxides from 1996 to 2014 constrained with satellite observations of NO2 columns
Geddes, Jeffrey A.1,3; Martin, Randall V.1,2
2017-08-29
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2017
卷号17期号:16
文章类型Article
语种英语
国家Canada; USA
英文摘要

Reactive nitrogen oxides(NOy) are a major constituent of the nitrogen deposited from the atmosphere, but observational constraints on their deposition are limited by poor or nonexistent measurement coverage in many parts of the world. Here we apply NO2 observations from multiple satellite instruments (GOME, SCIAMACHY, and GOME-2) to constrain the global deposition of NOy over the last 2 decades. We accomplish this by producing top-down estimates of NOx emissions from inverse modeling of satellite NO2 columns over 1996-2014, and including these emissions in the GEOS-Chem chemical transport model to simulate chemistry, transport, and deposition of NOy. Our estimates of long-term mean wet nitrate (NO3-) deposition are highly consistent with available measurements in North America, Europe, and East Asia combined (r = 0.83, normalized mean bias = -7 %, N = 136). Likewise, our calculated trends in wet NO3- deposition are largely consistent with the measurements, with 129 of the 136 gridded model-data pairs sharing overlapping 95% confidence intervals. We find that global mean NOy deposition over 1996-2014 is 56.0 Tg Ny r(-1), with a minimum in 2006 of 50.5 Tg N and a maximum in 2012 of 60.8 Tg N. Regional trends are large, with opposing signs in different parts of the world. Over 1996 to 2014, NOy deposition decreased by up to 60% in eastern North America, doubled in regions of East Asia, and declined by 20% in parts of western Europe. About 40% of the global NOy deposition occurs over oceans, with deposition to the North Atlantic Ocean declining and deposition to the northwestern Pacific Ocean increasing. Using the residual between NOx emissions and NOy deposition over specific land regions, we investigate how NOx export via atmospheric transport has changed over the last 2 decades. Net export from the continental United States decreased substantially, from 2.9 Tg N yr(-1) in 1996 to 1.5 Tg N yr(-1) in 2014. Export from China more than tripled between 1996 and 2011 (from 1.0 to 3.5 Tg N yr(-1)), before a striking decline to 2.5 Tg N yr(-1) by 2014. We find that declines in NOx export from some western European countries have counteracted increases in emissions from neighboring countries to the east. A sensitivity study indicates that simulated NOy deposition is robust to uncertainties in NH3 emissions with a few exceptions. Our novel long-term study provides timely context on the rapid redistribution of atmospheric nitrogen transport and subsequent deposition to ecosystems around the world.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000408534600001
WOS关键词LONG-RANGE TRANSPORT ; UNITED-STATES ; DRY DEPOSITION ; AIR-QUALITY ; EAST-ASIA ; TROPOSPHERIC NO2 ; DECADAL CHANGES ; SURFACE OZONE ; INTEX-B ; EMISSIONS
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/23858
专题地球科学
作者单位1.Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS, Canada;
2.Harvard Smithsonian Ctr Astrophys, 60 Garden St, Cambridge, MA 02138 USA;
3.Boston Univ, Dept Earth & Environm, Boston, MA 02215 USA
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GB/T 7714
Geddes, Jeffrey A.,Martin, Randall V.. Global deposition of total reactive nitrogen oxides from 1996 to 2014 constrained with satellite observations of NO2 columns[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2017,17(16).
APA Geddes, Jeffrey A.,&Martin, Randall V..(2017).Global deposition of total reactive nitrogen oxides from 1996 to 2014 constrained with satellite observations of NO2 columns.ATMOSPHERIC CHEMISTRY AND PHYSICS,17(16).
MLA Geddes, Jeffrey A.,et al."Global deposition of total reactive nitrogen oxides from 1996 to 2014 constrained with satellite observations of NO2 columns".ATMOSPHERIC CHEMISTRY AND PHYSICS 17.16(2017).
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