scholarly journals Detection of pollution transport events southeast of Mexico City using ground-based visible spectroscopy measurements of nitrogen dioxide

2009 ◽  
Vol 9 (1) ◽  
pp. 4769-4804 ◽  
Author(s):  
M. L. Melamed ◽  
R. Basaldud ◽  
R. Steinbrecher ◽  
S. Emeis ◽  
L. G. Ruíz-Suárez ◽  
...  

Abstract. This work presents ground based differential optical absorption spectroscopy (DOAS) measurements of nitrogen dioxide (NO2) during the MILAGRO field campaign in March 2006 at the Tenango del Aire research site located to the southeast of Mexico City. The DOAS NO2 column density measurements are used in conjunction with ceilometer, meteorological and surface nitrogen oxides (NOx) and total reactive nitrogen (NOy) measurements to show a more comprehensive view of air pollution results when a research site has both surface and remote sensing instruments. An in depth analysis of 13 March 2006 demonstrates how DOAS NO2, surface NO2 and ceilometer data can be used to determine the extent of mixing of the pollution layer. In addition, we show the effectiveness of how DOAS measurements can be used to observe pollution sources that may reside above the mixing layer, such as the presence of lightning produced NO2 as seen on 28 March 2006.

2009 ◽  
Vol 9 (14) ◽  
pp. 4827-4840 ◽  
Author(s):  
M. L. Melamed ◽  
R. Basaldud ◽  
R. Steinbrecher ◽  
S. Emeis ◽  
L. G. Ruíz-Suárez ◽  
...  

Abstract. This work presents ground based differential optical absorption spectroscopy (DOAS) measurements of nitrogen dioxide (NO2) during the MILAGRO field campaign in March 2006 at the Tenango del Aire research site located to the southeast of Mexico City. The DOAS NO2 column density measurements are used in conjunction with ceilometer, meteorological and surface nitric oxide (NO), nitrogen oxides (NOx) and total reactive nitrogen (NOy) measurements to analyze pollution transport events to the southeast of Mexico City during the MILARGO field campaign. The study divides the data set into three case study pollution transport events that occurred at the Tenango del Aire research site. The unique data set is then used to provide an in depth analysis of example days of each of the pollution transport events. An in depth analysis of 13 March 2006, a Case One day, shows the transport of several air pollution plumes during the morning through the Tenango del Aire research site when southerly winds are present and demonstrates how DOAS tropospheric NO2 vertical column densities (VCD), surface NO2 mixing ratios and ceilometer data are used to determine the vertical homogeneity of the pollution layer. The analysis of 18 March 2006, a Case Two day, shows that when northerly winds are present for the entire day, the air at the Tenango del Aire research site is relatively clean and no major pollution plumes are detected. Case 3 days are characterized by relatively clean air throughout the morning with large DOAS NO2 enhancements detected in the afternoon. The analysis of 28 March 2006 show the DOAS NO2 enhancements are likely due to lightning activity and demonstrate how suitable ground-based DOAS measruements are for monitoring anthropogenic and natural pollution sources that reside above the mixing layer.


2020 ◽  
Author(s):  
Claudia Rivera Cárdenas ◽  
Cesar Guarín ◽  
Wolfgang Stremme ◽  
Martina M. Friedrich ◽  
Alejandro Bezanilla ◽  
...  

Abstract. Formaldehyde (HCHO) total column densities over the Mexico City Metropolitan Area (MCMA) were retrieved using two independent measurement techniques: Multi Axis – Differential Optical Absorption Spectroscopy (MAX-DOAS) and Fourier Transform Infrared (FTIR) Spectroscopy. For the MAX-DOAS measurements, the software QDOAS was used to calculate differential Slant Column Densities (dSCDs) from the measured spectra and subsequently the Mexican MAX-DOAS Fit retrieval code (MMF) to convert from dSCDs to Vertical Column Densities (VCDs). The direct-solar absorption spectra measured with FTIR were analyzed using the PROFFIT retrieval code. Typically the MAX-DOAS instrument reports higher VCDs than those measured with FTIR, in part due to differences found in the ground-level sensitivities as revealed from the retrieval diagnostics from both instruments. Three MAX-DOAS datasets using measurements conducted towards the east, west or both sides of the measurement plane were evaluated with respect to the FTIR results. The retrieved MAX-DOAS HCHO VCDs where 5 %, 9 % and 28 % larger than the FTIR which, supported with satellite data, could demonstrate a large horizontal inhomogeneity in the HCHO abundances. A time-dependent comparison revealed that the vertical distribution of this pollutant, guided by the evolution of the mixing layer height, can play an important role in how the results are affected. Apart from the reported seasonal and diurnal variability of HCHO columns within the urban site, background data from measurements at a high-altitude station, located only 60 km away are presented.


2018 ◽  
Vol 11 (7) ◽  
pp. 4033-4058 ◽  
Author(s):  
Marina Zara ◽  
K. Folkert Boersma ◽  
Isabelle De Smedt ◽  
Andreas Richter ◽  
Enno Peters ◽  
...  

Abstract. Nitrogen dioxide (NO2) and formaldehyde (HCHO) column data from satellite instruments are used for air quality and climate studies. Both NO2 and HCHO have been identified as precursors to the ozone (O3) and aerosol essential climate variables, and it is essential to quantify and characterise their uncertainties. Here we present an intercomparison of NO2 and HCHO slant column density (SCD) retrievals from four different research groups (BIRA-IASB, IUP Bremen, and KNMI as part of the Quality Assurance for Essential Climate Variables (QA4ECV) project consortium, and NASA) and from the OMI and GOME-2A instruments. Our evaluation is motivated by recent improvements in differential optical absorption spectroscopy (DOAS) fitting techniques and by the desire to provide a fully traceable uncertainty budget for the climate data record generated within QA4ECV. The improved NO2 and HCHO SCD values are in close agreement but with substantial differences in the reported uncertainties between groups and instruments. To check the DOAS uncertainties, we use an independent estimate based on the spatial variability of the SCDs within a remote region. For NO2, we find the smallest uncertainties from the new QA4ECV retrieval (0.8  ×  1015 molec. cm−2 for both instruments over their mission lifetimes). Relative to earlier approaches, the QA4ECV NO2 retrieval shows better agreement between DOAS and statistical uncertainty estimates, suggesting that the improved QA4ECV NO2 retrieval has reduced but not altogether eliminated systematic errors in the fitting approach. For HCHO, we reach similar conclusions (QA4ECV uncertainties of 8–12  ×  1015 molec. cm−2), but the closeness between the DOAS and statistical uncertainty estimates suggests that HCHO uncertainties are indeed dominated by random noise from the satellite's level 1 data. We find that SCD uncertainties are smallest for high top-of-atmosphere reflectance levels with high measurement signal-to-noise ratios. From 2005 to 2015, OMI NO2 SCD uncertainties increase by 1–2 % year−1, which is related to detector degradation and stripes, but OMI HCHO SCD uncertainties are remarkably stable (increase  <  1 % year−1) and this is related to the use of Earth radiance reference spectra which reduces stripes. For GOME-2A, NO2 and HCHO SCD uncertainties increased by 7–9 and 11–15 % year−1 respectively up until September 2009, when heating of the instrument markedly reduced further throughput loss, stabilising the degradation of SCD uncertainty to  <  3 % year−1 for 2009–2015. Our work suggests that the NO2 SCD uncertainty largely consists of a random component ( ∼  65 % of the total uncertainty) as a result of the propagation of measurement noise but also of a substantial systematic component ( ∼  35 % of the total uncertainty) mainly from stripe effects. Averaging over multiple pixels in space and/or time can significantly reduce the SCD uncertainties. This suggests that trend detection in OMI, GOME-2 NO2, and HCHO time series is not limited by the spectral fitting but rather by the adequacy of assumptions on the atmospheric state in the later air mass factor (AMF) calculation step.


2018 ◽  
Author(s):  
Marina Zara ◽  
K. Folkert Boersma ◽  
Isabelle De Smedt ◽  
Andreas Richter ◽  
Enno Peters ◽  
...  

Abstract. Nitrogen dioxide (NO2) and formaldehyde (HCHO) column data from satellite instruments are used for air quality and climate studies. Both NO2 and HCHO have been identified as precursors to the ozone and aerosol Essential Climate Variables, and it is essential to quantify and characterize their uncertainties. Here we present an intercomparison of NO2 and HCHO slant column density (SCD) retrievals from 4 different research groups (BIRA-IASB, IUP, and KNMI as part of the Quality Assurance for Essential Climate Variables (QA4ECV) project consortium, and NASA) and from the OMI and GOME-2A instruments. Our evaluation is motivated by recent improvements in Differential Optical Absorption Spectroscopy (DOAS) fitting techniques, and by the desire to provide a fully traceable uncertainty budget for climate data record generated within QA4ECV. The improved NO2 and HCHO SCD values are in close agreement, but with substantial differences in the reported uncertainties between groups and instruments. As a check of the DOAS uncertainties, we use an independent estimate based on the spatial variability of the SCDs within a remote region. For NO2, we find the smallest uncertainties from the new QA4ECV retrieval (0.8 × 1015 molec. cm−2 for both instruments over their mission lifetimes). Relative to earlier approaches, the QA4ECV NO2 retrieval shows better agreement between DOAS and statistical uncertainty estimates, suggesting that the improved QA4ECV NO2 retrieval has reduced but not altogether eliminated systematic errors in the fitting approach. For HCHO, we reach similar conclusions (QA4ECV uncertainties of 8–12 × 1015 molec. cm−2 ), but the closure between the DOAS and statistical uncertainty estimates suggests that HCHO uncertainties are indeed dominated by random noise from the satellite’s level-1 data. We find that SCD uncertainties are smallest for high top-of-atmosphere reflectance levels. From 2005 to 2015, OMI NO2 SCD uncertainties increase by 1–2 %/yr related to detector degradation and stripes, but OMI HCHO SCD uncertainties are remarkably stable (increase


2021 ◽  
Vol 13 (10) ◽  
pp. 1937
Author(s):  
Yongjoo Choi ◽  
Yugo Kanaya ◽  
Hisahiro Takashima ◽  
Hitoshi Irie ◽  
Kihong Park ◽  
...  

We investigated long-term observations of the tropospheric nitrogen dioxide vertical column density (NO2 TropVCD) from the Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) network in Russia and ASia (MADRAS) from 2007 to 2017 at urban (Yokosuka and Gwangju) and remote (Fukue and Cape Hedo) sites in East Asia. The monthly mean in the NO2 TropVCD from MAX-DOAS measured at ~13:30 local time, which is the Ozone Monitoring Instrument (OMI) overpass time, shows good agreement with OMI data during summer, but differences between the two datasets increase in winter. The Theil-Sen slope of the long-term trend indicate a relatively rapid and gradual reduction in NO2 at Yokosuka and two remote sites (Fukue and Cape Hedo), respectively, regardless of the season except for fall at Fukue, but significant changes in NO2 are not observed at Gwangju, Korea. In contrast, OMI satellite data reveal an increase in the NO2 TropVCD at all sites except for Yokosuka, where a decreasing trend common to MAX-DOAS is found, suggesting that the results from satellites need to be cautiously used for investigating long-term trends in less polluted or remote areas. Using backward trajectories, potential source regions are identified for the two urban sites. The spatial distribution from OMI data shows good agreement with the potential source regions at Yokosuka. The potential source regions in Gwangju are identified as the National Industrial Complex in Yeosu and Gwangyang, while the transport route is not clearly visible with OMI data because of their low sensitivity in less polluted areas. The proposed approach is suitable for identifying potential source areas that might not be recognized by satellite observations.


2021 ◽  
Vol 13 (12) ◽  
pp. 2244
Author(s):  
Zeeshan Javed ◽  
Aimon Tanvir ◽  
Muhammad Bilal ◽  
Wenjing Su ◽  
Congzi Xia ◽  
...  

Recently, the occurrence of fog and haze over China has increased. The retrieval of trace gases from the multi-axis differential optical absorption spectroscopy (MAX-DOAS) is challenging under these conditions. In this study, various reported retrieval settings for formaldehyde (HCHO) and sulfur dioxide (SO2) are compared to evaluate the performance of these settings under different meteorological conditions (clear day, haze, and fog). The dataset from 1st December 2019 to 31st March 2020 over Nanjing, China, is used in this study. The results indicated that for HCHO, the optimal settings were in the 324.5–359 nm wavelength window with a polynomial order of five. At these settings, the fitting and root mean squared (RMS) errors for column density were considerably improved for haze and fog conditions, and the differential slant column densities (DSCDs) showed more accurate values compared to the DSCDs between 336.5 and 359 nm. For SO2, the optimal settings for retrieval were found to be at 307–328 nm with a polynomial order of five. Here, root mean square (RMS) and fitting errors were significantly lower under all conditions. The observed HCHO and SO2 vertical column densities were significantly lower on fog days compared to clear days, reflecting a decreased chemical production of HCHO and aqueous phase oxidation of SO2 in fog droplets.


2007 ◽  
Vol 7 (5) ◽  
pp. 15025-15065 ◽  
Author(s):  
W. J. Shaw ◽  
M. S. Pekour ◽  
R. L. Coulter ◽  
T. J. Martin ◽  
J. T. Walters

Abstract. During the MILAGRO campaign centered in the Mexico City area, Pacific Northwest National Laboratory (PNNL) and Argonne National Laboratory (ANL) operated atmospheric profiling systems at Veracruz and at two locations on the Central Mexican Plateau in the region around Mexico City. These systems included radiosondes, wind profilers, a sodar, and an aerosol backscatter lidar. An additional wind profiler was operated by the University of Alabama in Huntsville (UAH) at the Mexican Petroleum Institue (IMP) near the center of Mexico City. Because of the opportunity afforded by collocation of profilers, radiosondes, and a lidar, and because of the importance of boundary layer depth for aerosol properties, we have carried out a comparison of mixing layer depth as determined independently from these three types of measurement systems during the campaign. We have then used results of this comparison and additional measurements to develop a detailed description of the daily structure and evolution of the boundary layer on the Central Mexican Plateau during MILAGRO. Our analysis indicates that the profilers were more consistently successful in establishing the mixing layer depth during the daytime. The boundary layer growth was similar at the three locations, although the mixing layer tended to be slightly deeper in the afternoon in central Mexico City. The sodar showed that convection began about an hour after sunrise. Maximum daily mixing layer depths always reached 2000 m a.g.l. and frequently extended to 4000 m. The rate and variability of mixing layer growth was essentially the same as that observed during the IMADA-AVER campaign in the same season in 1997. This growth did not seem to be related to whether deep convection was reported on a given day. Wind speeds within the boundary layer exhibited a daily low-altitude maximum in the late afternoon with lighter winds aloft, consistent with previous reports of diurnal regional circulations. Norte events, which produced high winds at Veracruz, did not appreciably modulate the winds on the plateau. Finally, despite the typically dry conditions at the surface, radiosonde profiles showed that relative humidity often exceeded 50% in the early morning and in the upper part of the boundary layer. This suggests that aerosol particles would have experienced hygroscopic growth within the boundary layer on many days.


2015 ◽  
Vol 221 (1) ◽  
pp. 2 ◽  
Author(s):  
J. Xavier Prochaska ◽  
John M. O’Meara ◽  
Michele Fumagalli ◽  
Rebecca A. Bernstein ◽  
Scott M. Burles

Sign in / Sign up

Export Citation Format

Share Document