Ground-level nitrogen dioxide concentrations inferred from the satellite-borne Ozone Monitoring Instrument

被引:301
作者
Lamsal, L. N. [1 ]
Martin, R. V. [1 ,2 ]
van Donkelaar, A. [1 ]
Steinbacher, M. [3 ]
Celarier, E. A. [4 ]
Bucsela, E.
Dunlea, E. J. [5 ]
Pinto, J. P. [6 ]
机构
[1] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada
[2] Smithsonian Astrophys Observ, Harvard Smithsonian Ctr Astrophys, Atom & Mol Phys Div, Cambridge, MA USA
[3] Empa, Swiss Fed Labs Mat Testing & Res, Swiss Fed Inst Mat Sci & Technol, Lab Air Pollut Environm Technol, CH-8600 Dubendorf, Switzerland
[4] NASA, Goddard Space Flight Ctr, SGT Inc, Greenbelt, MD 20770 USA
[5] MIT, Dept Earth Atmospher & Planetary Sci, Cambridge, MA USA
[6] US EPA, Natl Ctr Environm Assessment, Res Triangle Pk, NC 27711 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
D O I
10.1029/2007JD009235
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
We present an approach to infer ground-level nitrogen dioxide (NO2) concentrations by applying local scaling factors from a global three-dimensional model (GEOS-Chem) to tropospheric NO2 columns retrieved from the Ozone Monitoring Instrument (OMI) onboard the Aura satellite. Seasonal mean OMI surface NO2 derived from the standard tropospheric NO2 data product (Version 1.0.5, Collection 3) varies by more than two orders of magnitude (< 0.1-> 10 ppbv) over North America. Two ground-based data sets are used to validate the surface NO2 estimate and indirectly validate the OMI tropospheric NO2 retrieval: photochemical steady-state (PSS) calculations of NO2 based on in situ NO and O-3 measurements, and measurements from a commercial chemiluminescent NO2 analyzer equipped with a molybdenum converter. An interference correction algorithm for the latter is developed using laboratory and field measurements and applied using modeled concentrations of the interfering species. The OMI-derived surface NO2 mixing ratios are compared with an in situ surface NO2 data obtained from the U. S. Environmental Protection Agency's Air Quality System (AQS) and Environment Canada's National Air Pollution Surveillance (NAPS) network for 2005 after correcting for the interference in the in situ data. The overall agreement of the OMI-derived surface NO2 with the corrected in situ measurements and PSS-NO2 is -11-36%. A larger difference in winter/spring than in summer/fall implies a seasonal bias in the OMI NO2 retrieval. The correlation between the OMI-derived surface NO2 and the ground-based measurements is significant (correlation coefficient up to 0.86) with a tendency for higher correlations in polluted areas. The satellite-derived data base of ground level NO2 concentrations could be valuable for assessing exposures of humans and vegetation to NO2, supplementing the capabilities of the ground-based networks, and evaluating air quality models and the effectiveness of air quality control strategies.
引用
收藏
页数:15
相关论文
共 91 条
[1]   Cloud pressure retrieval using the O2-O2 absorption band at 477 nm -: art. no. D05204 [J].
Acarreta, JR ;
De Haan, JF ;
Stammes, P .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D5)
[2]   Lung function and long term exposure to air pollutants in Switzerland [J].
AckermannLiebrich, U ;
Leuenberger, P ;
Schwartz, J ;
Schindler, C ;
Monn, C ;
Bolognini, C ;
Bongard, JP ;
Brandli, O ;
Domenighetti, G ;
Elsasser, S ;
Grize, L ;
Karrer, W ;
Keller, R ;
KellerWossidlo, H ;
Kunzli, N ;
Martin, BW ;
Medici, TC ;
Perruchoud, AP ;
Schoni, MH ;
Tschopp, JM ;
Villiger, B ;
Wuthrich, B ;
Zellweger, JP ;
Zemp, E .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 155 (01) :122-129
[3]   An evaluation of the FAST-J photolysis algorithm for predicting nitrogen dioxide photolysis rates under clear and cloudy sky conditions [J].
Barnard, JC ;
Chapman, EG ;
Fast, JD ;
Schmelzer, JR ;
Slusser, JR ;
Shetter, RE .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (21) :3393-3403
[4]   Weekly cycle of NO2 by GOME measurements:: a signature of anthropogenic sources [J].
Beirle, S ;
Platt, U ;
Wenig, M ;
Wagner, T .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2003, 3 :2225-2232
[5]   Global modeling of tropospheric chemistry with assimilated meteorology: Model description and evaluation [J].
Bey, I ;
Jacob, DJ ;
Yantosca, RM ;
Logan, JA ;
Field, BD ;
Fiore, AM ;
Li, QB ;
Liu, HGY ;
Mickley, LJ ;
Schultz, MG .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2001, 106 (D19) :23073-23095
[6]   Validation of OMI tropospheric NO2 observations during INTEX-B and application to constrain NOx emissions over the eastern United States and Mexico [J].
Boersma, K. F. ;
Jacob, D. J. ;
Bucsela, E. J. ;
Perring, A. E. ;
Dirksen, R. ;
van der A, R. J. ;
Yantosca, R. M. ;
Park, R. J. ;
Wenig, M. O. ;
Bertram, T. H. ;
Cohen, R. C. .
ATMOSPHERIC ENVIRONMENT, 2008, 42 (19) :4480-4497
[7]  
Boersma K.F., 2002, OMI ALGORITHM THEORE, V4
[8]   Intercomparison of SCIAMACHY and OMI tropospheric NO2 columns:: Observing the diurnal evolution of chemistry and emissions from space [J].
Boersma, K. Folkert ;
Jacob, Daniel J. ;
Eskes, Henk J. ;
Pinder, Robert W. ;
Wang, Jun ;
van der A, Ronald J. .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2008, 113 (D16)
[9]   Error analysis for tropospheric NO2 retrieval from space -: art. no. D04311 [J].
Boersma, KF ;
Eskes, HJ ;
Brinksma, EJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D4)
[10]  
Bovensmann H, 1999, J ATMOS SCI, V56, P127, DOI 10.1175/1520-0469(1999)056<0127:SMOAMM>2.0.CO