Vertical profiles of trace gases in the troposphere over South Asia

2022 ◽  
pp. 303-322
Author(s):  
L.K. Sahu ◽  
P.R. Sinha
Keyword(s):  
South Asia ◽  
Trace Gases ◽  
Vertical Profiles

Clear-sky vertical profiles of trace gases as influenced by upstream convective activity

1989 ◽  
Vol 94 (D12) ◽  
pp. 14879-14892 ◽  
Author(s):  
Kenneth E. Pickering ◽  
Russell R. Dickerson ◽  
Winston T. Luke ◽  
Linda J. Nunnermacker
Keyword(s):  
Trace Gases ◽  
Vertical Profiles ◽  
Convective Activity ◽  
Clear Sky

Distribution of reactive trace gases over South Asia: Observations and modeling

2022 ◽  
pp. 147-169
Author(s):  
Narendra Ojha ◽  
Imran Girach ◽  
Meghna Soni ◽  
Narendra Singh
Keyword(s):  
South Asia ◽  
Trace Gases ◽  
Reactive Trace Gases

scholarly journals Vertical profiles of NO<sub>2</sub>, SO<sub>2</sub>, HONO, HCHO, CHOCHO, and aerosols derived from MAX-DOAS measurements at a rural site in the central-western North China Plain and their relation to emission sources and effects of regional transport

2018 ◽  
Author(s):  
Yang Wang ◽  
Steffen Dörner ◽  
Sebastian Donner ◽  
Sebastian Böhnke ◽  
Isabelle De Smedt ◽  
...  
Keyword(s):  
Trace Gases ◽  
Rural Site ◽  
Optical Absorption Spectroscopy ◽  
Vertical Profiles ◽  
Regional Transport ◽  
Near Surface ◽  
North West ◽  
Mixing Ratios ◽  
Chemistry Research

Abstract. A Multi Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) instrument was deployed in May and June 2016 at a monitoring station (37.18° N, 114.36° E) in the suburban area of Xingtai (one of the most polluted cities in China) during the Atmosphere-Aerosol-Boundary Layer-Cloud (A2BC) and Air chemistry Research In Asia (ARIAs) joint experiments to derive tropospheric vertical profiles of NO2, SO2, HONO, HCHO, CHOCHO and aerosols. Aerosol optical depths derived from MAX-DOAS were found to be consistent with collocated sun-photometer measurements. Also the derived near-surface aerosol extinction and HCHO mixing ratio agree well with coincident visibility meter and in situ HCHO measurements, with mean HCHO near-surface mixing ratios of ~ 3.5 ppb. Underestimates of MAX-DOAS results compared to in situ measurements of NO2 (~ 60 %), SO2 (~ 20 %) are found expectedly due to vertical and horizontal inhomogeneity of trace gases. Vertical profiles of aerosols and NO2, SO2 are reasonably consistent with those measured by a collocated Raman Lidar and aircraft spirals over the station. The deviations can be attributed to differences in sensitivity as a function of altitude and substantial horizontal gradients of pollutants. Aerosols, HCHO, and CHOCHO profiles typically extended to higher altitudes (with 75 % integrated column located below ~ 1.4 km) than did NO2, SO2, and HONO (with 75 % integrated column below ~ 0.5 km) under polluted condition. Lifted layers were systematically observed for all species, (except HONO), indicating accumulation, secondary formation, or long-range transport of the pollutants at higher altitudes. Maximum values routinely occurred in the morning for NO2, SO2, and HONO, but around noon for aerosols, HCHO, and CHOCHO, mainly dominated by photochemistry, characteristic upslope/downslope circulation and PBL dynamics. Significant day-to-day variations are found for all species due to the effect of regional transport and changes in synoptic pattern analysed with HYSPLIT trajectories. Low pollution was often observed for air masses from the north-west (behind cold fronts), and high pollution from the southern areas such as industrialized Wuan. The contribution of regional transport for the pollutants measured at the site during the observation period was estimated to be about 20 % to 30 % for trace gases, and about 50 % for aerosols. In addition, agricultural burning events impacted the day-to-day variations of HCHO, CHOCHO and aerosols.

scholarly journals Estimate of bias in Aura TES HDO/H<sub>2</sub>O profiles from comparison of TES and in situ HDO/H<sub>2</sub>O measurements at the Mauna Loa observatory

2011 ◽  
Vol 11 (9) ◽  
pp. 4491-4503 ◽  
Author(s):  
J. Worden ◽  
D. Noone ◽  
J. Galewsky ◽  
A. Bailey ◽  
K. Bowman ◽  
...  
Keyword(s):  
Bias Correction ◽  
Trace Gases ◽  
Lower Troposphere ◽  
Vertical Profiles ◽  
Thermal Contrast ◽  
Near Surface ◽  
Mauna Loa ◽  
In Situ Data ◽  
Infrared Radiances

Abstract. The Aura satellite Tropospheric Emission Spectrometer (TES) instrument is capable of measuring the HDO/H2O ratio in the lower troposphere using thermal infrared radiances between 1200 and 1350 cm−1. However, direct validation of these measurements is challenging due to a lack of in situ measured vertical profiles of the HDO/H2O ratio that are spatially and temporally co-located with the TES observations. From 11 October through 5 November 2008, we undertook a campaign to measure HDO and H2O at the Mauna Loa observatory in Hawaii for comparison with TES observations. The Mauna Loa observatory is situated at 3.1 km above sea level or approximately 680 hPa, which is approximately the altitude where the TES HDO/H2O observations show the most sensitivity. Another advantage of comparing in situ data from this site to estimates derived from thermal IR radiances is that the volcanic rock is heated by sunlight during the day, thus providing significant thermal contrast between the surface and atmosphere; this thermal contrast increases the sensitivity to near surface estimates of tropospheric trace gases. The objective of this inter-comparison is to better characterize a bias in the TES HDO data, which had been previously estimated to be approximately 5 % too high for a column integrated value between 850 hPa and 500 hPa. We estimate that the TES HDO profiles should be corrected downwards by approximately 4.8 % and 6.3 % for Versions 3 and 4 of the data respectively. These corrections must account for the vertical sensitivity of the TES HDO estimates. We estimate that the precision of this bias correction is approximately 1.9 %. The accuracy is driven by the corrections applied to the in situ HDO and H2O measurements using flask data taken during the inter-comparison campaign and is estimated to be less than 1 %. Future comparisons of TES data to accurate vertical profiles of in situ measurements are needed to refine this bias estimate.

scholarly journals The CU Airborne MAX-DOAS instrument: vertical profiling of aerosol extinction and trace gases

2013 ◽  
Vol 6 (3) ◽  
pp. 719-739 ◽  
Author(s):  
S. Baidar ◽  
H. Oetjen ◽  
S. Coburn ◽  
B. Dix ◽  
I. Ortega ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Air Quality ◽  
Spatial Scales ◽  
Trace Gases ◽  
Stray Light ◽  
Aerosol Extinction ◽  
Vertical Profiles ◽  
Maximum Information ◽  
Extinction Coefficients

Abstract. The University of Colorado Airborne Multi-Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS) instrument uses solar stray light to detect and quantify multiple trace gases, including nitrogen dioxide (NO2), glyoxal (CHOCHO), formaldehyde (HCHO), water vapor (H2O), nitrous acid (HONO), iodine monoxide (IO), bromine monoxide (BrO), and oxygen dimers (O4) at multiple wavelengths (absorption bands at 360, 477, 577, 632 nm) simultaneously in the open atmosphere. The instrument is unique as it (1) features a motion compensation system that decouples the telescope field of view from aircraft movements in real time (<0.35° accuracy), and (2) includes measurements of solar stray light photons from nadir, zenith, and multiple elevation angles forward and below the plane by the same spectrometer/detector system. Sets of solar stray light spectra collected from nadir to zenith scans provide some vertical profile information within 2 km above and below the aircraft altitude, and the vertical column density (VCD) below the aircraft is measured in nadir view. Maximum information about vertical profiles is derived simultaneously for trace gas concentrations and aerosol extinction coefficients over similar spatial scales and with a vertical resolution of typically 250 m during aircraft ascent/descent. The instrument is described, and data from flights over California during the CalNex (California Research at the Nexus of Air Quality and Climate Change) and CARES (Carbonaceous Aerosols and Radiative Effects Study) air quality field campaigns is presented. Horizontal distributions of NO2 VCD (below the aircraft) maps are sampled with typically 1 km resolution, and show good agreement with two ground-based MAX-DOAS instruments (slope = 0.95 ± 0.09, R2 = 0.86). As a case study vertical profiles of NO2, CHOCHO, HCHO, and H2O concentrations and aerosol extinction coefficients, ε, at 477 nm calculated from O4 measurements from a low approach at Brackett airfield inside the South Coast Air Basin (SCAB) are presented. These profiles contain ~12 degrees of freedom (DOF) over a 3.5 km altitude range, an independent information approximately every 250 m. The boundary layer NO2 concentration, and the integral aerosol extinction over height (aerosol optical depth, AOD) agrees well with nearby ground-based in situ NO2 measurement, and AERONET station. The detection limits of NO2, CHOCHO, HCHO, H2O442, &amp;varepsilon;360, &amp;varepsilon;477 for 30 s integration time spectra recorded forward of the plane are 5 ppt, 3 ppt, 100 ppt, 42 ppm, 0.004 km−1, 0.002 km−1 in the free troposphere (FT), and 30 ppt, 16 ppt, 540 ppt, 252 ppm, 0.012 km−1, 0.006 km−1 inside the boundary layer (BL), respectively. Mobile column observations of trace gases and aerosols are complimentary to in situ observations, and help bridge the spatial scales that are probed by satellites and ground-based observations, and predicted by atmospheric models.

scholarly journals Simulation of trace gases and aerosols over the Indian domain: evaluation of the WRF-Chem Model

2013 ◽  
Vol 13 (5) ◽  
pp. 12287-12336 ◽  
Author(s):  
M. Michael ◽  
A. Yadav ◽  
S. N. Tripathi ◽  
V. P. Kanawade ◽  
A. Gaur ◽  
...  
Keyword(s):  
Sulfur Dioxide ◽  
Black Carbon ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Indian Subcontinent ◽  
Trace Gases ◽  
Atmospheric Composition ◽  
Emission Rates ◽  
Vertical Profiles ◽  
Monsoon Period

Abstract. The "online" meteorological and chemical transport Weather Research and Forecasting/Chemistry (WRF-Chem) model has been implemented over the Indian subcontinent for three consecutive summers in 2008, 2009 and 2010 to study the aerosol properties over the domain. The initial and boundary conditions are obtained from NCAR reanalysis data. The emission rates of sulfur dioxide, black carbon, organic carbon and PM2.5, which are developed over India at a grid resolution of 0.25° × 0.25° have been used in the present study. The remaining emissions are obtained from global inventories (RETRO and EDGAR). The model simulated the meteorological parameters, trace gases and particulate matter. Predicted mixing ratios of trace gases (Ozone, carbon monoxide and sulfur dioxide) are compared with ground based observations over Kanpur. Simulated aerosol optical depth are compared with those observed at nine Aerosol Robotic Network stations (AERONET). The simulations show that the aerosol optical depth of the less polluted regions is better simulated compared to that of the locations where the aerosol loading is very high. The vertical profiles of extinction coefficient observed at Kanpur Micropulse Lidar Network (MPLNET) station is in agreement with the simulated values for altitudes greater than 1.5 km and qualitatively simulate the elevated layers of aerosols. The simulated mass concentration of black carbon shows very good correlation with observations, due to the better local emission inventory used. The vertical profiles of black carbon at various locations have also been compared with observations from aircraft campaign held during pre-monsoon period of 2008 and 2009 resulting in good agreement. This study shows that WRF-Chem model captures many important features of the observations and therefore can be used for understanding and predicting regional atmospheric composition over Indian subcontinent.

Source apportionment of surface-level trace gases and particulate matter at three tropical coastal sites in India

2021 ◽  
Author(s):  
Abhishek Chhari ◽  
Vinay Kumar Dhadwal ◽  
Lokesh Kumar Sahu ◽  
Bomidi Lakshmi Madhavan ◽  
Trupti Das ◽  
...  
Keyword(s):  
Particulate Matter ◽  
Air Quality ◽  
South Asia ◽  
Mass Concentration ◽  
Trace Gases ◽  
Concentration Data ◽  
Gangetic Plain ◽  
Surface Mass ◽  
Temporal And Spatial ◽  
Significant Attention

&lt;p&gt;Over last two decades, South Asia has witnessed a rapid increase in population, industrialization, and energy demands. Consequently, 2-6 fold increase in the emission of particulate matter (PM) and trace gases were reported. Air pollution in South Asia has more adverse impact and is linked to nearly 1 million premature deaths and around 10 million tonnes of crop loss in a year. So, monitoring of trace gases and PM concentrations over urban centers has received significant attention among scientists, policymakers, health regulatory agencies, and the media. Particularly over the Indian region, this becomes significant, as the observation of trace gases and PM concentrations with fairly good temporal and spatial resolutions is limited. Concerns about air quality and transport pathways on a regional scale also place more stringent demand on observations and modeling effort. Quantifying the source contribution (regional emission due to various anthropogenic activities such as city traffic density vs. long-range transport due to meteorological influence) of trace gases and PM over different temporal and spatial scales has been receiving significant attention. In view of this, measurement of trace gases and PM in concurrence with meteorological variables (wind speed and direction) is of paramount importance.&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;&lt;p&gt;In this study, we have presented three-year surface measurements of TGs (O&lt;sub&gt;3&lt;/sub&gt;, CO, NO&lt;sub&gt;x&lt;/sub&gt;, SO&lt;sub&gt;2&lt;/sub&gt; and NH&lt;sub&gt;3&lt;/sub&gt;) and PMs (PM2.5 and PM10) at three coastal and urban sites, namely, Trivandrum (TVM, 8.5&amp;#176;N, 76.9&amp;#176;E, 5m AMSL), Chennai (CHN, 13.7&amp;#176;N, 80.2&amp;#176;E, 6.7m AMSL) and Bhubaneswar (BHB, 20.2&amp;#176;N, 85.8&amp;#176;E, 45m AMSL) located in India. -In addition to that Ozone Monitoring Instrument OMI&amp;#8217;s, surface mass concentration data for SO&lt;sub&gt;2&lt;/sub&gt; and Moderate Resolution Imaging Spectroradiometer (MODIS) fire counts data were also used to identify potential sources. The principal component analysis (PCA) and concentrated weighted trajectories (CWT) were applied to the dataset. The TGs and PM showed high values during winter and lower values in a monsoon at these sites. Both TGs and PM values were higher at BHB compared to those at TVM and CHN.&amp;#160; Surface O&lt;sub&gt;3&lt;/sub&gt; at BHB was about 3 times higher than that at TVM and 2.2 times higher than that at CHN.&amp;#160; Interestingly, PCA suggests that the major concentrations of O&lt;sub&gt;3&lt;/sub&gt;, PM10, and SO&lt;sub&gt;2&lt;/sub&gt; at TVM and CHN were transported from different locations and not produced locally except for pre-monsoon at CHN, which was of local origin.&amp;#160; CWT analysis and OMI&amp;#8217;s surface mass concentration data also suggest that the air quality at TVM could be influenced by heavy emissions transported from the Indo-Gangetic plain. The Merra-2 reanalysis well captured seasonal variations of TGs and PMs; and it overestimated surface O&lt;sub&gt;3&lt;/sub&gt;, by a factor of about 2 to the measurement at the study sites.&amp;#160;&amp;#160;&amp;#160;&lt;/p&gt;

Vertical Profiles of Long Lived Trace Gases

2000 ◽  
pp. 241-244
Author(s):  
Melanie Müller ◽  
Martin Strunk ◽  
Andreas Engel ◽  
Ulrich Schmidt
Keyword(s):  
Trace Gases ◽  
Vertical Profiles

A method for retrieving the spatial distribution of trace gases using measurements of three ground-based MAX-DOAS instruments

2020 ◽  
Author(s):  
Michael Revesz ◽  
Stefan F. Schreier ◽  
Philipp Weihs ◽  
Tim Bösch ◽  
Kezia Lange ◽  
...  
Keyword(s):  
Spatial Distribution ◽  
Vertical Distribution ◽  
Trace Gases ◽  
Trace Gas ◽  
Wind Condition ◽  
Vertical Profiles ◽  
Open Issue ◽  
Using Data ◽  
Set Up ◽  
The Vertical Distribution

&lt;p&gt;Within the project VINDOBONA (VIenna horizontal aNd vertical Distribution OBservations Of Nitrogen dioxide and Aerosols), a method was developed to retrieve the spatial distribution of trace gases using data from three ground based MAX-DOAS instruments and was applied on the example of NO&lt;sub&gt;2&lt;/sub&gt;. At three different locations in Vienna (Austria) MAX-DOAS instruments were installed performing measurements in the visible and UV spectral range. Currently, each instrument is set up to determine the column densities in different azimuthal directions and low elevation angles within approximately a horizontal plane. The different lines of sight of the three instruments intersect horizontally and can be used to estimate the horizontal spatial distribution of trace gases. With the knowledge of vertical profiles, even the vertical distribution can be estimated using this method.&amp;#160;&lt;/p&gt;&lt;p&gt;The intersections of the different lines of sight define segments along the slant columns for which the mass concentrations can be estimated. Knowledge about the vertical profiles for a chosen trace gas can be used to correct the retrieved trace gas concentration to specific altitudes above ground. Such corrections are also required since the three instruments were set up at different heights above ground, at different altitudes relative to sea level and with different elevation angles of the lowest viewing direction. One open issue for the retrieval process is the terrain in Vienna in combination with the prevailing wind condition that impacts the horizontal and vertical trace gas distribution and make the retrieval challenging.&amp;#160;&lt;/p&gt;

scholarly journals Simulation of trace gases and aerosols over the Indian domain: evaluation of the WRF-Chem model

2014 ◽  
Vol 7 (1) ◽  
pp. 431-482 ◽  
Author(s):  
M. Michael ◽  
A. Yadav ◽  
S. N. Tripathi ◽  
V. P. Kanawade ◽  
A. Gaur ◽  
...  
Keyword(s):  
Black Carbon ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Indian Subcontinent ◽  
Monsoon Season ◽  
Trace Gases ◽  
Atmospheric Composition ◽  
Vertical Profiles ◽  
Monsoon Period ◽  
Mixing Ratios

Abstract. The "online" meteorological and chemical transport Weather Research and Forecasting/Chemistry (WRF-Chem) model has been implemented over the Indian subcontinent for three consecutive summers in 2008, 2009 and 2010 to study the aerosol properties over the domain. The model simulated the meteorological parameters, trace gases and particulate matter. Predicted mixing ratios of trace gases (Ozone, carbon monoxide and sulfur dioxide) are compared with ground based observations over Kanpur. Simulated aerosol optical depth are compared with those observed at nine Aerosol Robotic Network stations (AERONET). The simulations show that the aerosol optical depth of the less polluted regions is better simulated compared to that of the locations where the aerosol loading is very high. The vertical profiles of extinction coefficient observed at the Kanpur Micropulse Lidar Network (MPLNET) station is underpredicted by the model by 10 to 50% for altitudes greater than 1.5 km and qualitatively simulate the elevated layers of aerosols. The simulated mass concentration of black carbon shows a correlation coefficient of 0.4 with observations. Vertical profiles of black carbon at various locations have also been compared with observations from an aircraft campaign held during pre-monsoon period of 2008 and 2009. This study shows that WRF-Chem model captures many important features of the observed atmospheric composition during the pre-monsoon season in India.

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