scholarly journals Validation of Ozone Monitoring Instrument nitrogen dioxide columns

Author(s):  
E. A. Celarier ◽  
E. J. Brinksma ◽  
J. F. Gleason ◽  
J. P. Veefkind ◽  
A. Cede ◽  
...  
2021 ◽  
Vol 14 (1) ◽  
pp. 455-479
Author(s):  
Lok N. Lamsal ◽  
Nickolay A. Krotkov ◽  
Alexander Vasilkov ◽  
Sergey Marchenko ◽  
Wenhan Qin ◽  
...  

Abstract. We present a new and improved version (V4.0) of the NASA standard nitrogen dioxide (NO2) product from the Ozone Monitoring Instrument (OMI) on the Aura satellite. This version incorporates the most salient improvements for OMI NO2 products suggested by expert users and enhances the NO2 data quality in several ways through improvements to the air mass factors (AMFs) used in the retrieval algorithm. The algorithm is based on the geometry-dependent surface Lambertian equivalent reflectivity (GLER) operational product that is available on an OMI pixel basis. GLER is calculated using the vector linearized discrete ordinate radiative transfer (VLIDORT) model, which uses as input high-resolution bidirectional reflectance distribution function (BRDF) information from NASA's Aqua Moderate Resolution Imaging Spectroradiometer (MODIS) instruments over land and the wind-dependent Cox–Munk wave-facet slope distribution over water, the latter with a contribution from the water-leaving radiance. The GLER combined with consistently retrieved oxygen dimer (O2–O2) absorption-based effective cloud fraction (ECF) and optical centroid pressure (OCP) provide improved information to the new NO2 AMF calculations. The new AMFs increase the retrieved tropospheric NO2 by up to 50 % in highly polluted areas; these differences arise from both cloud and surface BRDF effects as well as biases between the new MODIS-based and previously used OMI-based climatological surface reflectance data sets. We quantitatively evaluate the new NO2 product using independent observations from ground-based and airborne instruments. The new V4.0 data and relevant explanatory documentation are publicly available from the NASA Goddard Earth Sciences Data and Information Services Center (https://disc.gsfc.nasa.gov/datasets/OMNO2_V003/summary/, last access: 8 November 2020), and we encourage their use over previous versions of OMI NO2 products.


2010 ◽  
Vol 44 (11) ◽  
pp. 1443-1448 ◽  
Author(s):  
Yasuko Yoshida ◽  
Bryan N. Duncan ◽  
Christian Retscher ◽  
Kenneth E. Pickering ◽  
Edward A. Celarier ◽  
...  

2015 ◽  
Vol 120 (11) ◽  
pp. 5670-5692 ◽  
Author(s):  
S. Marchenko ◽  
N. A. Krotkov ◽  
L. N. Lamsal ◽  
E. A. Celarier ◽  
W. H. Swartz ◽  
...  

2014 ◽  
Vol 14 (3) ◽  
pp. 1441-1461 ◽  
Author(s):  
J.-T. Lin ◽  
R. V. Martin ◽  
K. F. Boersma ◽  
M. Sneep ◽  
P. Stammes ◽  
...  

Abstract. Retrievals of tropospheric nitrogen dioxide (NO2) from the Ozone Monitoring Instrument (OMI) are subject to errors in the treatments of aerosols, surface reflectance anisotropy, and vertical profile of NO2. Here we quantify the influences over China via an improved retrieval process. We explicitly account for aerosol optical effects (simulated by nested GEOS-Chem at 0.667° long. × 0.5° lat. and constrained by aerosol measurements), surface reflectance anisotropy, and high-resolution vertical profiles of NO2 (simulated by GEOS-Chem). Prior to the NO2 retrieval, we derive the cloud information using consistent ancillary assumptions. We compare our retrieval to the widely used DOMINO v2 product, using MAX-DOAS measurements at three urban/suburban sites in East China as reference and focusing the analysis on the 127 OMI pixels (in 30 days) closest to the MAX-DOAS sites. We find that our retrieval reduces the interference of aerosols on the retrieved cloud properties, thus enhancing the number of valid OMI pixels by about 25%. Compared to DOMINO v2, our retrieval better captures the day-to-day variability in MAX-DOAS NO2 data (R2 = 0.96 versus 0.72), due to pixel-specific radiative transfer calculations rather than the use of a look-up table, explicit inclusion of aerosols, and consideration of surface reflectance anisotropy. Our retrieved NO2 columns are 54% of the MAX-DOAS data on average, reflecting the inevitable spatial inconsistency between the two types of measurement, errors in MAX-DOAS data, and uncertainties in our OMI retrieval related to aerosols and vertical profile of NO2. Sensitivity tests show that excluding aerosol optical effects can either increase or decrease the retrieved NO2 for individual OMI pixels with an average increase by 14%. Excluding aerosols also complexly affects the retrievals of cloud fraction and particularly cloud pressure. Employing various surface albedo data sets slightly affects the retrieved NO2 on average (within 10%). The retrieved NO2 columns increase when the NO2 profiles are taken from MAX-DOAS retrievals (by 19% on average) or TM4 simulations (by 13%) instead of GEOS-Chem simulations. Our findings are also relevant to retrievals of other pollutants (e.g., sulfur dioxide, ormaldehyde, glyoxal) from UV–visible backscatter satellite instruments.


2013 ◽  
Vol 13 (8) ◽  
pp. 21203-21257 ◽  
Author(s):  
J.-T. Lin ◽  
R. V. Martin ◽  
K. F. Boersma ◽  
M. Sneep ◽  
P. Stammes ◽  
...  

Abstract. Retrievals of tropospheric nitrogen dioxide (NO2) from the Ozone Monitoring Instrument (OMI) are subject to errors in the treatments of aerosols, surface reflectance anisotropy, and vertical profile of NO2. Here we quantify the influences over China via an improved retrieval process. We explicitly account for aerosol optical effects (simulated by nested GEOS-Chem at 0.667° lon × 0.5° lat and constrained by aerosol measurements), surface reflectance anisotropy, and high-resolution vertical profiles of NO2 (simulated by GEOS-Chem). Prior to the NO2 retrieval, we derive the cloud information using consistent ancillary assumptions. We compare our retrieval to the widely used DOMINO v2 product, using as reference MAX-DOAS measurements at three urban/suburban sites in East China and focusing the analysis on the 127 OMI pixels (in 30 days) closest to the MAX-DOAS sites. We find that our retrieval reduces the interference of aerosols on the retrieved cloud properties, thus enhancing the number of valid OMI pixels by about 25%. Compared to DOMINO v2, our retrieval improves the correlation with the MAX-DOAS data in the day-to-day variability of NO2 (R2 = 0.96 vs. 0.72). Our retrieved NO2 columns are about 50% of the MAX-DOAS data on average. This reflects the inevitable spatial inconsistency between the two types of measurement, uncertainties in MAX-DOAS data, and residual uncertainties in our OMI retrievals related to aerosols and vertical profile of NO2. Through a series of tests, we find that excluding aerosol scattering/absorption can either increase or decrease the retrieved NO2, with a mean absolute difference by about 20%. Concentrating aerosols at the boundary layer top enhances the retrieved NO2 by 8% on average with a mean absolute difference by 23%. The aerosol perturbations also affect nonlinearly the retrieved cloud fraction and particularly cloud pressure. Employing various surface albedo datasets alters the retrieved NO2 by 0–7% on average. The retrieved NO2 columns increase when the NO2 profiles are taken from MAX-DOAS retrievals (by 20% on average) or TM4 simulations (by 10%) instead of GEOS-Chem simulations. Our findings are also relevant to retrievals of other pollutants (e.g., sulfur dioxide, formaldehyde, glyoxal) from UV-vis backscatter satellite instruments.


2014 ◽  
Vol 5 (4) ◽  
pp. 686-695 ◽  
Author(s):  
Fengjie Zheng ◽  
Tao Yu ◽  
Tianhai Cheng ◽  
Xingfa Gu ◽  
Hong Guo

Author(s):  
L. N. Lamsal ◽  
R. V. Martin ◽  
A. van Donkelaar ◽  
M. Steinbacher ◽  
E. A. Celarier ◽  
...  

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