scholarly journals High spatial resolution measurements of NO<sub>2</sub> applying Topographic Target Light scattering-Differential Optical Absorption Spectroscopy (ToTaL-DOAS)

2008 ◽  
Vol 8 (24) ◽  
pp. 7595-7601 ◽  
Author(s):  
E. Frins ◽  
U. Platt ◽  
T. Wagner
Keyword(s):  
Light Scattering ◽  
Optical Absorption ◽  
Spatial Resolution ◽  
Absorption Spectroscopy ◽  
High Spatial Resolution ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Air Masses ◽  
Target Light ◽  
Mixing Ratios

Abstract. Topographic Target Light scattering – Differential Optical Absorption Spectroscopy (ToTaL-DOAS), also called Target-DOAS, is a novel experimental procedure to retrieve trace gas concentrations present in the low atmosphere. Scattered sunlight (diffuse or specular) reflected from natural or artificial targets located at different distances are analyzed to retrieve the spatial distribution of the concentration of different trace gases like NO2, SO2 and others. We report high spatial resolution measurements of NO2 mixing ratios in the city of Montevideo (Uruguay) observing three buildings as targets with a Mini-DOAS instrument. Our instrument was 146 m, 196 m, and 280 m apart from three different buildings located along a main Avenue. We obtain temporal variation of NO2 mixing ratios between 30 ppb and 65 ppb from measurements of November 2007 and mixing ratios up to 50 ppb from measurements of August and September 2008. Our measurements demonstrate that ToTaL-DOAS observations can be made over relative short distances. In polluted air masses, the retrieved absorption signal was found to be sufficiently strong to allow measurements over distances in the range of several tens of meters.

scholarly journals High spatial resolution measurements of NO<sub>2</sub> applying Topographic Target Light scattering-Differential Optical Absorption Spectroscopy (ToTaL-DOAS)

2008 ◽  
Vol 8 (3) ◽  
pp. 10257-10273
Author(s):  
E. Frins ◽  
U. Platt ◽  
T. Wagner
Keyword(s):  
Light Scattering ◽  
Optical Absorption ◽  
Spatial Resolution ◽  
Absorption Spectroscopy ◽  
High Spatial Resolution ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Air Masses ◽  
Target Light ◽  
Mixing Ratios

Abstract. Tomographic Target Light scattering – Differential Optical Absorption Spectroscopy (ToTaL-DOAS), also called Target-DOAS, is a novel experimental procedure to retrieve trace gas concentrations present in the low atmosphere. Scattered sunlight (partially or totally) reflected from natural or artificial targets of similar albedo located at different distances is analyzed to retrieve the concentration of different trace gases like NO2, SO2 and others. We report high spatial resolution measurements of NO2 mixing ratios in the city of Montevideo (Uruguay) observing three buildings as targets with a Mini-DOAS instrument. Our instrument was 146 m apart from the first building, 196 m from the second and 286 m from the third one. All three buildings are located along a main Avenue. We obtain temporal variation of NO2 mixing ratios between 30 ppb and 65 ppb (±2 ppb). Our measurements demonstrate that ToTaL-DOAS measurements can be made over very short distances. In polluted air masses, the retrieved absorption signal was found to be strong enough to allow measurements over distances in the range of several ten meters, and achieve a spatial resolution of 50 m approximately.

scholarly journals MAX-DOAS detection of glyoxal during ICARTT 2004

2007 ◽  
Vol 7 (5) ◽  
pp. 1293-1303 ◽  
Author(s):  
R. Sinreich ◽  
R. Volkamer ◽  
F. Filsinger ◽  
U. Frieß ◽  
C. Kern ◽  
...  
Keyword(s):  
Optical Absorption ◽  
Absorption Spectroscopy ◽  
Gulf Of Maine ◽  
Direct Detection ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Massachusetts Institute Of Technology ◽  
Mixing Ratios ◽  
Institute Of Technology ◽  
Methodological Aspects

Abstract. The direct detection of glyoxal (CHOCHO), the smallest α-dicarbonyl, in the open atmosphere by active differential optical absorption spectroscopy (DOAS) has recently been demonstrated (Volkamer et al., 2005a) and triggered the very recent successful detection of CHOCHO from space (Kurosu et al., 2005; Wittrock et al., 2006; Beirle et al., 2006). Here we report the first comprehensive analysis of CHOCHO by passive multi axis differential optical absorption spectroscopy (MAX-DOAS). CHOCHO and NO2 slant column measurements were conducted at the Massachusetts Institute of Technology (MIT), Cambridge, USA, and on board the research vessel Ron Brown in the Gulf of Maine as part of the International Consortium for Atmospheric Research on Transport and Transformation (ICARTT) 2004 campaign. For a day with nearly clear sky conditions, radiative transfer modeling was employed to derive diurnal CHOCHO mixing ratios in the planetary boundary layer (PBL) for both sites. CHOCHO mixing ratios at MIT varied from 40 to 140 ppt, with peak values observed around noon. Mixing ratios over the Gulf of Maine were found to be up to 2.5 times larger than at MIT. The CHOCHO-to-NO2 ratio at MIT was <0.03, and enhancements of this ratio by up to two orders of magnitude were found over the Gulf of Maine. This paper focuses on the methodological aspects involved with MAX-DOAS measurements of CHOCHO.

scholarly journals The spatial distribution of the reactive iodine species IO from simultaneous active and passive DOAS observations

2009 ◽  
Vol 9 (5) ◽  
pp. 21371-21398 ◽  
Author(s):  
K. Seitz ◽  
J. Buxmann ◽  
D. Pöhler ◽  
T. Sommer ◽  
J. Tschritter ◽  
...  
Keyword(s):  
Optical Absorption ◽  
Absorption Spectroscopy ◽  
Coastal Region ◽  
Horizontal Distribution ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Research Station ◽  
Intertidal Area ◽  
Mixing Ratios ◽  
Iodine Species

Abstract. We present investigations of the reactive iodine species (RIS) IO, OIO and I2 in a coastal region from a field campaign simultaneously employing active long path differential optical absorption spectroscopy (LP-DOAS) as well as passive multi-axis differential optical absorption spectroscopy (MAX-DOAS). The campaign took place at the Martin Ryan Institute (MRI) in Carna, County Galway at the Irish West Coast about 6 km south-east of the atmospheric research station Mace Head in summer 2007. In order to study the horizontal distribution of the trace gases of interest, we established two almost parallel active LP-DOAS light paths, the shorter of 1034 m length just crossing the intertidal area, whereas the longer one of 3946 m length also crossed open water during periods of low tide. In addition we operated two passive Mini-MAX-DOAS instruments with the same viewing direction. While neither OIO nor I2 could be unambiguously identified with any of the instruments, IO could be detected with active as well as passive DOAS. The IO column densities seen at both active LP-DOAS light paths are almost the same. Thus it can be concluded that coastal IO is almost exclusively located in the intertidal area, where we detected mixing ratios of up to 35±7.7 ppt (equivalent to pmol/mol). Nucleation events with particle concentrations of 106 cm−3 particles were observed each day correlating with high IO mixing ratios. Therefore we feel that our detected IO concentrations confirm the results of model studies, which state that in order to explain such particle bursts, IO mixing ratios of 50 to 100 ppt in so called "hot-spots" are required.

scholarly journals Studies of the horizontal inhomogeneities in NO<sub>2</sub> concentrations above a shipping lane using ground-based multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements and validation with airborne imaging DOAS measurements

2019 ◽  
Vol 12 (11) ◽  
pp. 5959-5977 ◽  
Author(s):  
André Seyler ◽  
Andreas C. Meier ◽  
Folkard Wittrock ◽  
Lisa Kattner ◽  
Barbara Mathieu-Üffing ◽  
...  
Keyword(s):  
Optical Absorption ◽  
Absorption Spectroscopy ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Northerly Wind ◽  
Airborne Measurements ◽  
Mixing Ratios ◽  
The North ◽  
Airborne Imaging ◽  
Spectral Ranges

Abstract. This study describes a novel application of an “onion-peeling” approach to multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements of shipping emissions aiming at investigating the strong horizontal inhomogeneities in NO2 over a shipping lane. To monitor ship emissions on the main shipping route towards the port of Hamburg, a two-channel (UV and visible) MAX-DOAS instrument was deployed on the island Neuwerk in the German Bight, 6–7 km south of the main shipping lane. Utilizing the fact that the effective light path length in the atmosphere depends systematically on wavelength, simultaneous measurements and DOAS retrievals in the UV and visible spectral ranges are used to probe air masses at different horizontal distances to the instrument to estimate two-dimensional pollutant distributions. Two case studies have been selected to demonstrate the ability to derive the approximate plume positions in the observed area. A situation with northerly wind shows high NO2 concentrations close to the measurement site and low values in the north of the shipping lane. The opposite situation with southerly wind, unfavorable for the on-site in situ instrumentation, demonstrates the ability to detect enhanced NO2 concentrations several kilometers away from the instrument. Using a Gaussian plume model, in-plume NO2 volume mixing ratios can be derived from the MAX-DOAS measurements. For validation, a comparison to airborne imaging DOAS measurements during the NOSE campaign in July 2013 is performed, showing good agreement between the approximate plume position derived from the onion-peeling MAX-DOAS and the airborne measurements as well as between the derived in-plume NO2 volume mixing ratios (VMRs).

scholarly journals The spatial distribution of the reactive iodine species IO from simultaneous active and passive DOAS observations

2010 ◽  
Vol 10 (5) ◽  
pp. 2117-2128 ◽  
Author(s):  
K. Seitz ◽  
J. Buxmann ◽  
D. Pöhler ◽  
T. Sommer ◽  
J. Tschritter ◽  
...  
Keyword(s):  
Optical Absorption ◽  
Absorption Spectroscopy ◽  
Coastal Region ◽  
Horizontal Distribution ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Research Station ◽  
Intertidal Area ◽  
Mixing Ratios ◽  
Iodine Species

Abstract. We present investigations of the reactive iodine species (RIS) IO, OIO and I2 in a coastal region from a field campaign simultaneously employing active long path differential optical absorption spectroscopy (LP-DOAS) as well as passive multi-axis differential optical absorption spectroscopy (MAX-DOAS). The campaign took place at the Martin Ryan Institute (MRI) in Carna, County Galway at the Irish West Coast about 6 km south-east of the atmospheric research station Mace Head in summer 2007. In order to study the horizontal distribution of the trace gases of interest, we established two almost parallel active LP-DOAS light paths, the shorter of 1034 m length just crossing the intertidal area, whereas the longer one of 3946 m length also crossed open water during periods of low tide. In addition we operated two passive Mini-MAX-DOAS instruments with the same viewing direction. While neither OIO nor I2 could be unambiguously identified with any of the instruments, IO could be detected with active as well as passive DOAS. The IO column densities seen at both active LP-DOAS light paths are almost the same. Thus it can be concluded that coastal IO is almost exclusively located in the intertidal area, where we detected mixing ratios of up to 29±8.8 ppt (equivalent to pmol/mol). Nucleation events with particle concentrations of 106 cm−3 particles were observed each day correlating with high IO mixing ratios. Therefore we feel that our detected IO concentrations confirm the results of model studies, which state that in order to explain such particle bursts, IO mixing ratios of 50 to 100 ppt in so called "hot-spots" are required.

scholarly journals A new Differential Optical Absorption Spectroscopy instrument to study atmospheric chemistry from a high-altitude unmanned aircraft

2017 ◽  
Vol 10 (3) ◽  
pp. 1017-1042 ◽  
Author(s):  
Jochen Stutz ◽  
Bodo Werner ◽  
Max Spolaor ◽  
Lisa Scalone ◽  
James Festa ◽  
...  
Keyword(s):  
Radiative Transfer ◽  
Optical Absorption ◽  
High Altitude ◽  
Absorption Spectroscopy ◽  
Unmanned Aircraft ◽  
Differential Optical Absorption Spectroscopy ◽  
Lower Atmosphere ◽  
Optical Absorption Spectroscopy ◽  
Mixing Ratios ◽  
Tropical Tropopause

Abstract. Observations of atmospheric trace gases in the tropical upper troposphere (UT), tropical tropopause layer (TTL), and lower stratosphere (LS) require dedicated measurement platforms and instrumentation. Here we present a new limb-scanning Differential Optical Absorption Spectroscopy (DOAS) instrument developed for NASA's Global Hawk (GH) unmanned aerial system and deployed during the Airborne Tropical TRopopause EXperiment (ATTREX). The mini-DOAS system is designed for automatic operation under unpressurized and unheated conditions at 14–18 km altitude, collecting scattered sunlight in three wavelength windows: UV (301–387 nm), visible (410–525 nm), and near infrared (900–1700 nm). A telescope scanning unit allows selection of a viewing angle around the limb, as well as real-time correction of the aircraft pitch. Due to the high altitude, solar reference spectra are measured using diffusors and direct sunlight. The DOAS approach allows retrieval of slant column densities (SCDs) of O3, O4, NO2, and BrO with relative errors similar to other aircraft DOAS systems. Radiative transfer considerations show that the retrieval of trace gas mixing ratios from the observed SCD based on O4 observations, the most common approach for DOAS measurements, is inadequate for high-altitude observations. This is due to the frequent presence of low-altitude clouds, which shift the sensitivity of the O4 SCD into the lower atmosphere and make it highly dependent on cloud coverage. A newly developed technique that constrains the radiative transfer by comparing in situ and DOAS O3 observations overcomes this issue. Extensive sensitivity calculations show that the novel O3-scaling technique allows the retrieval of BrO and NO2 mixing ratios at high accuracies of 0.5 and 15 ppt, respectively. The BrO and NO2 mixing ratios and vertical profiles observed during ATTREX thus provide new insights into ozone and halogen chemistry in the UT, TTL, and LS.

scholarly journals A New Differential Optical Absorption Spectroscopy Instrument to Study Atmospheric Chemistry from a High-Altitude Unmanned Aircraft

2016 ◽  
Author(s):  
Jochen Stutz ◽  
Bodo Werner ◽  
Max Spolaor ◽  
Lisa Scalone ◽  
James Festa ◽  
...  
Keyword(s):  
Radiative Transfer ◽  
Optical Absorption ◽  
High Altitude ◽  
Absorption Spectroscopy ◽  
Atmospheric Chemistry ◽  
Unmanned Aircraft ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Mixing Ratios ◽  
Tropical Tropopause

Abstract. Observations of atmospheric trace gases in the tropical upper troposphere (UT), tropical tropopause layer (TTL) and lower stratosphere (LS) require dedicated measurement platforms and instrumentation. Here we present a new limb-scanning Differential Optical Absorption Spectroscopy (DOAS) instrument developed for NASA’s Global Hawk unmanned aerial system (GH) during the Airborne Tropical TRopopause EXperiment (ATTREX). The mini-DOAS system is designed for automatic operation under unpressurized and unheated conditions at 14–18 km altitude, collecting scattered sunlight in three wavelength windows: UV (301–387 nm), visible (410–525 nm) and near infrared (900–1700 nm). A telescope scanning unit allows selection of a viewing angle around the limb, as well as real-time correction of the aircraft pitch. Due to the high altitude, solar reference spectra are measured using diffusors and direct sunlight. The DOAS approach allows retrieval of slant column densities (SCD) of O3, O4, NO2, and BrO with relative errors similar to other aircraft DOAS systems. Radiative transfer considerations show that the retrieval of trace gas mixing ratios from the observed SCD based on O4 observations, the most common approach for DOAS measurements, is inadequate for high-altitude observations, due to frequent presence of low altitude clouds. A newly developed technique that constrains the radiative transfer (RT) by comparing in-situ and DOAS O3 observations overcomes this issue. Extensive sensitivity calculations show that the novel O3-scaling technique allows the retrieval of BrO and NO2 mixing ratios at high accuracies of 0.3–0.6 ppt and 15 ppt, respectively. The BrO and NO2 mixing ratios and vertical profiles observed during ATTREX thus provide new insights into ozone and halogen chemistry in the UT, TTL, and LS.

scholarly journals MAX-DOAS detection of glyoxal during ICARTT 2004

2006 ◽  
Vol 6 (5) ◽  
pp. 9459-9481 ◽  
Author(s):  
R. Sinreich ◽  
R. Volkamer ◽  
F. Filsinger ◽  
U. Frieß ◽  
C. Kern ◽  
...  
Keyword(s):  
Optical Absorption ◽  
Absorption Spectroscopy ◽  
Gulf Of Maine ◽  
Direct Detection ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Transport And Transformation ◽  
Mixing Ratios ◽  
Clear Sky ◽  
Sky Conditions

Abstract. The direct detection of glyoxal (CHOCHO), the smallest α-dicarbonyl, in the open atmosphere by active differential optical absorption spectroscopy (DOAS) has recently been demonstrated (Volkamer et al., 2005a) and triggered the very recent successful detection of CHOCHO from space (Kurosu et al., 2005; Wittrock et al., 2006; Beirle et al., 2006). Here we report the first detection of CHOCHO by passive multi axis differential optical absorption spectroscopy (MAX-DOAS). CHOCHO and NO2 slant column measurements were conducted at MIT, Cambridge, USA, and on board the research vessel Ron Brown in the Gulf of Maine as part of the International Consortium for Atmospheric Research on Transport and Transformation (ICARTT) 2004 campaign. For a day with nearly clear sky conditions, radiative transfer modeling was employed to derive diurnal CHOCHO mixing ratios for both sites. CHOCHO mixing ratios at MIT varied from 40 to 120 ppt, with peak values observed around noon. Mixing ratios over the Gulf of Maine were found to be up to 3 times larger than at MIT. The CHOCHO-to-NO2ratio at MIT was <0.03, and enhancements of this ratio by up to two orders of magnitude were found over the Gulf of Maine. This paper focuses on the instrumental aspects involved with MAX-DOAS measurements of CHOCHO.

scholarly journals NO<sub>2</sub> measurements in Hong Kong using LED based long path differential optical absorption spectroscopy

2012 ◽  
Vol 5 (5) ◽  
pp. 901-912 ◽  
Author(s):  
K. L. Chan ◽  
D. Pöhler ◽  
G. Kuhlmann ◽  
A. Hartl ◽  
U. Platt ◽  
...  
Keyword(s):  
Hong Kong ◽  
Optical Absorption ◽  
Absorption Spectroscopy ◽  
Differential Optical Absorption Spectroscopy ◽  
Optical Absorption Spectroscopy ◽  
Ozone Monitoring Instrument ◽  
Data Set ◽  
Weekly Cycle ◽  
Mixing Ratios

Abstract. In this study we present the first long term measurements of atmospheric nitrogen dioxide (NO2) using a LED based Long Path Differential Optical Absorption Spectroscopy (LP-DOAS) instrument. This instrument is measuring continuously in Hong Kong since December 2009, first in a setup with a 550 m absorption path and then with a 3820 m path at about 30 m to 50 m above street level. The instrument is using a high power blue light LED with peak intensity at 450 nm coupled into the telescope using a Y-fibre bundle. The LP-DOAS instrument measures NO2 levels in the Kowloon Tong and Mongkok district of Hong Kong and we compare the measurement results to mixing ratios reported by monitoring stations operated by the Hong Kong Environmental Protection Department in that area. Hourly averages of coinciding measurements are in reasonable agreement (R = 0.74). Furthermore, we used the long-term data set to validate the Ozone Monitoring Instrument (OMI) NO2 data product. Monthly averaged LP-DOAS and OMI measurements correlate well (R = 0.84) when comparing the data for the OMI overpass time. We analyzed weekly patterns in both data sets and found that the LP-DOAS detects a clear weekly cycle with a reduction on weekends during rush hour peaks, whereas OMI is not able to observe this weekly cycle due to its fix overpass time (13:30–14:30 LT – local time).

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