scholarly journals Review of Dix et al., Parameterization Retrieval of Trace Gas Volume Mixing Ratios from Airborne MAX-DOAS

2016 ◽  
Author(s):  
Anonymous
Keyword(s):  
Trace Gas ◽  
Mixing Ratios ◽  
Gas Volume

scholarly journals CRISTA-NF measurements with unprecedented vertical resolution during the RECONCILE aircraft campaign

2012 ◽  
Vol 5 (5) ◽  
pp. 1173-1191 ◽  
Author(s):  
J. Ungermann ◽  
C. Kalicinsky ◽  
F. Olschewski ◽  
P. Knieling ◽  
L. Hoffmann ◽  
...  
Keyword(s):  
Cross Sections ◽  
Polar Vortex ◽  
The Arctic ◽  
Trace Gas ◽  
Retrieval Algorithm ◽  
Vertical Resolution ◽  
Mixing Ratios ◽  
Flight Direction ◽  
Research Aircraft ◽  
Gas Volume

Abstract. The Cryogenic Infrared Spectrometers and Telescope for the Atmosphere – New Frontiers (CRISTA-NF), an airborne infrared limb-sounder, was operated aboard the high-flying Russian research aircraft M55-Geophysica during the Arctic RECONCILE campaign from January to March 2010. This paper describes the calibration process of the instrument and the retrieval algorithm employed and then proceeds to present retrieved trace gas volume mixing ratio cross-sections for one specific flight in this campaign. We are able to resolve the uppermost troposphere/lower stratosphere for several trace gas species for several kilometres below the flight altitude (16 to 19 km) with an unprecedented vertical resolution of 400 to 500 m for the limb-sounding technique. The instrument points sideways with respect to the flight direction. Therefore, the observations are also characterised by a rather high horizontal sampling along the flight track, which provides a full vertical profile every ≈15 km. Assembling the vertical trace gas profiles derived from CRISTA-NF measurements to cross-sections shows filaments of vortex and extra-vortex air masses in the vicinity of the polar vortex. During this campaign, the M55-Geophysica carried further instruments enabling trace gas volume mixing ratios derived from CRISTA-NF to be validated by comparing them with measurements by the in situ instruments HAGAR and FOZAN and observations by MIPAS-STR. This validation suggests that the retrieved trace gas volume mixing ratios are both qualitatively and quantitatively reliable.

scholarly journals Variation Characteristics and Transportation of Aerosol, NO2, SO2, and HCHO in Coastal Cities of Eastern China: Dalian, Qingdao, and Shanghai

2021 ◽  
Vol 13 (5) ◽  
pp. 892
Author(s):  
Xiaomei Li ◽  
Pinhua Xie ◽  
Ang Li ◽  
Jin Xu ◽  
Zhaokun Hu ◽  
...  
Keyword(s):  
Eastern China ◽  
Temporal Distribution ◽  
Correlation Coefficients ◽  
Optical Absorption Spectroscopy ◽  
Near Surface ◽  
Mixing Ratios ◽  
Variation Characteristics ◽  
Spatio Temporal ◽  
Gas Volume ◽  
Transport Flux

This paper studied the method for converting the aerosol extinction to the mass concentration of particulate matter (PM) and obtained the spatio-temporal distribution and transportation of aerosol, nitrogen dioxide (NO2), sulfur dioxide (SO2), and formaldehyde (HCHO) based on multi-axis differential optical absorption spectroscopy (MAX-DOAS) observations in Dalian (38.85°N, 121.36°E), Qingdao (36.35°N, 120.69°E), and Shanghai (31.60°N, 121.80°E) from 2019 to 2020. The PM2.5 measured by the in situ instrument and the PM2.5 simulated by the conversion formula showed a good correlation. The correlation coefficients R were 0.93 (Dalian), 0.90 (Qingdao), and 0.88 (Shanghai). A regular seasonality of the three trace gases is found, but not for aerosols. Considerable amplitudes in the weekly cycles were determined for NO2 and aerosols, but not for SO2 and HCHO. The aerosol profiles were nearly Gaussian, and the shapes of the trace gas profiles were nearly exponential, except for SO2 in Shanghai and HCHO in Qingdao. PM2.5 presented the largest transport flux, followed by NO2 and SO2. The main transport flux was the output flux from inland to sea in spring and winter. The MAX-DOAS and the Copernicus Atmosphere Monitoring Service (CAMS) models’ results were compared. The overestimation of NO2 and SO2 by CAMS is due to its overestimation of near-surface gas volume mixing ratios.

scholarly journals Characterization of Transport Regimes and the Polar Dome during Arctic Spring and Summer using in-situ Aircraft Measurements

2019 ◽  
Author(s):  
Heiko Bozem ◽  
Peter Hoor ◽  
Daniel Kunkel ◽  
Franziska Köllner ◽  
Johannes Schneider ◽  
...  
Keyword(s):  
Lower Troposphere ◽  
High Arctic ◽  
The Arctic ◽  
Trace Gas ◽  
Second Phase ◽  
Aerosol Formation ◽  
Transport Barrier ◽  
Data Set ◽  
Air Masses ◽  
Mixing Ratios

Abstract. The springtime composition of the Arctic lower troposphere is to a large extent controlled by transport of mid-latitude air masses into the Arctic, whereas during the summer precipitation and natural sources play the most important role. Within the Arctic region, there exists a transport barrier, known as the polar dome, which results from sloping isentropes. The polar dome, which varies in space and time, exhibits a strong influence on the transport of air masses from mid-latitudes, enhancing it during winter and inhibiting it during summer. Furthermore, a definition for the location of the polar dome boundary itself is quite sparse in the literature. We analyzed aircraft based trace gas measurements in the Arctic during two NETCARE airborne field camapigns (July 2014 and April 2015) with the Polar 6 aircraft of Alfred Wegener Institute Helmholtz Center for Polar and Marine Research (AWI), Bremerhaven, Germany, covering an area from Spitsbergen to Alaska (134° W to 17° W and 68° N to 83° N). For the spring (April 2015) and summer (July 2014) season we analyzed transport regimes of mid-latitude air masses travelling to the high Arctic based on CO and CO2 measurements as well as kinematic 10-day back trajectories. The dynamical isolation of the high Arctic lower troposphere caused by the transport barrier leads to gradients of chemical tracers reflecting different local chemical life times and sources and sinks. Particularly gradients of CO and CO2 allowed for a trace gas based definition of the polar dome boundary for the two measurement periods with pronounced seasonal differences. For both campaigns a transition zone rather than a sharp boundary was derived. For July 2014 the polar dome boundary was determined to be 73.5° N latitude and 299–303.5 K potential temperature, respectively. During April 2015 the polar dome boundary was on average located at 66–68.5° N and 283.5–287.5 K. Tracer-tracer scatter plots and probability density functions confirm different air mass properties inside and outside of the polar dome for the July 2014 and April 2015 data set. Using the tracer derived polar dome boundaries the analysis of aerosol data indicates secondary aerosol formation events in the clean summertime polar dome. Synoptic-scale weather systems frequently disturb this transport barrier and foster exchange between air masses from midlatitudes and polar regions. During the second phase of the NETCARE 2014 measurements a pronounced low pressure system south of Resolute Bay brought inflow from southern latitudes that pushed the polar dome northward and significantly affected trace gas mixing ratios in the measurement region. Mean CO mixing ratios increased from 77.9 ± 2.5 ppbv to 84.9 ± 4.7 ppbv from the first period to the second period. At the same time CO2 mixing ratios significantly dropped from 398.16 ± 1.01 ppmv to 393.81 ± 2.25 ppmv. We further analysed processes controlling the recent transport history of air masses within and outside the polar dome. Air masses within the spring time polar dome mainly experienced diabatic cooling while travelling over cold surfaces. In contrast air masses in the summertime polar dome were diabatically heated due to insolation. During both seasons air masses outside the polar dome slowly descended into the Arctic lower troposphere from above caused by radiative cooling. The ascent to the middle and upper troposphere mainly took place outside the Arctic, followed by a northward motion. Our results demonstrate the successful application of a tracer based diagnostic to determine the location of the polar dome boundary.

scholarly journals Structural changes in the shallow and transition branch of the Brewer–Dobson circulation induced by El Niño

2018 ◽  
Author(s):  
Mohamadou Diallo ◽  
Paul Konopka ◽  
Michelle L. Santee ◽  
Rolf Müller ◽  
Mengchu Tao ◽  
...  
Keyword(s):  
El Niño ◽  
Structural Changes ◽  
Lower Stratosphere ◽  
Transport Model ◽  
El Nino ◽  
Southern Oscillation ◽  
Satellite Observations ◽  
Trace Gas ◽  
Residual Circulation ◽  
Mixing Ratios

Abstract. The stratospheric Brewer–Dobson circulation (BD-circulation) determines the transport and lifetime of key radiatively active trace gases and further impacts surface climate through downward coupling. Here, we quantify the variability in the lower stratospheric BD-circulation induced by the El Nino Southern Oscillation (ENSO), using satellite trace gas measurements and simulations with the Lagrangian chemistry transport model, CLaMS, driven by ERA-Interim and JRA-55 reanalyses. We show that despite discrepancies in the deseasonalised ozone (O3) mixing ratios between CLaMS simulations and satellite observations, the patterns of changes in the lower stratospheric O3 anomalies induced by ENSO agree remarkably well over the 2005–2016 period. Particularly during the most recent El Niño in 2015–2016, both satellite observations and CLaMS simulations show the largest negative tropical O3 anomaly in the record. Regression analysis of different metrics of the BD-circulation strength, including mean age of air, vertical velocity, residual circulation and age spectrum, shows clear evidence for structural changes of the BD-circulation in the lower stratosphere induced by El Niño, consistent with observed O3 anomalies. These structural changes during El Niño include a weakening of the transition branch of the BD-circulation between about 370–420 K (∼ 100–70 hPa) and equatorward of about 60° and, a strengthening of the shallow branch at the same latitudes and between about 420–500 K (∼ 70–30 hPa). The strengthening of the shallow branch induces negative tropical O3 anomalies due to enhanced tropical upwelling, while the weakening of the transition branch combined with enhanced downwelling due to the strengthening shallow branch leads to positive O3 anomalies in the extratropical upper troposphere-lower stratosphere (UTLS). Our results suggest that a shift of the ENSO basic state toward more frequent El Niño-like conditions in a warming future climate will substantially alter UTLS trace gas distributions due to these changes in the vertical structure of the stratospheric circulation.

scholarly journals Level 2 processing for the imaging Fourier transform spectrometer GLORIA: derivation and validation of temperature and trace gas volume mixing ratios from calibrated dynamics mode spectra

2015 ◽  
Vol 8 (6) ◽  
pp. 2473-2489 ◽  
Author(s):  
J. Ungermann ◽  
J. Blank ◽  
M. Dick ◽  
A. Ebersoldt ◽  
F. Friedl-Vallon ◽  
...  
Keyword(s):  
Fourier Transform ◽  
Horizontal Resolution ◽  
Trace Gas ◽  
Radiative Transfer Model ◽  
Transfer Model ◽  
Ionization Mass ◽  
Fourier Transform Spectrometer ◽  
Upper Troposphere ◽  
Mixing Ratios

Abstract. The Gimballed Limb Observer for Radiance Imaging of the Atmosphere (GLORIA) is an airborne infrared limb imager combining a two-dimensional infrared detector with a Fourier transform spectrometer. It was operated aboard the new German Gulfstream G550 High Altitude LOng Range (HALO) research aircraft during the Transport And Composition in the upper Troposphere/lowermost Stratosphere (TACTS) and Earth System Model Validation (ESMVAL) campaigns in summer 2012. This paper describes the retrieval of temperature and trace gas (H2O, O3, HNO3) volume mixing ratios from GLORIA dynamics mode spectra that are spectrally sampled every 0.625 cm−1. A total of 26 integrated spectral windows are employed in a joint fit to retrieve seven targets using consecutively a fast and an accurate tabulated radiative transfer model. Typical diagnostic quantities are provided including effects of uncertainties in the calibration and horizontal resolution along the line of sight. Simultaneous in situ observations by the Basic Halo Measurement and Sensor System (BAHAMAS), the Fast In-situ Stratospheric Hygrometer (FISH), an ozone detector named Fairo, and the Atmospheric chemical Ionization Mass Spectrometer (AIMS) allow a validation of retrieved values for three flights in the upper troposphere/lowermost stratosphere region spanning polar and sub-tropical latitudes. A high correlation is achieved between the remote sensing and the in situ trace gas data, and discrepancies can to a large extent be attributed to differences in the probed air masses caused by different sampling characteristics of the instruments. This 1-D processing of GLORIA dynamics mode spectra provides the basis for future tomographic inversions from circular and linear flight paths to better understand selected dynamical processes of the upper troposphere and lowermost stratosphere.

scholarly journals Validation of MIPAS IMK/IAA methane profiles

2015 ◽  
Vol 8 (12) ◽  
pp. 5251-5261 ◽  
Author(s):  
A. Laeng ◽  
J. Plieninger ◽  
T. von Clarmann ◽  
U. Grabowski ◽  
G. Stiller ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Michelson Interferometer ◽  
European Space Agency ◽  
Trace Gas ◽  
Mixing Ratios ◽  
Air Sampler ◽  
Solar Occultation ◽  
Space Agency ◽  
Scanning Imaging ◽  
Satellite Instruments

Abstract. The Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) is an infrared (IR) limb emission spectrometer on the Envisat platform. It measures trace gas distributions during day and night, pole-to-pole, over an altitude range from 6 to 70 km in nominal mode and up to 170 km in special modes, depending on the measurement mode, producing more than 1000 profiles day−1. We present the results of a validation study of methane, version V5R_CH4_222, retrieved with the IMK/IAA (Institut für Meteorologie und Klimaforschung, Karlsruhe/Instituto de Astrofisica de Andalucia, Grenada) MIPAS scientific level 2 processor. The level 1 spectra are provided by the ESA (European Space Agency) and version 5 was used. The time period covered is 2005–2012, which corresponds to the period when MIPAS measured trace gas distributions at a reduced spectral resolution of 0.0625 cm−1. The comparison with satellite instruments includes the Atmospheric Chemistry Experiment Fourier Transform Spectrometer (ACE-FTS), the HALogen Occultation Experiment (HALOE), the Solar Occultation For Ice Experiment (SOFIE) and the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY). Furthermore, comparisons with MkIV balloon-borne solar occultation measurements and with air sampling measurements performed by the University of Frankfurt are presented. The validation activities include bias determination, assessment of stability, precision validation, analysis of histograms and comparison of corresponding climatologies. Above 50 km altitude, MIPAS methane mixing ratios agree within 3 % with ACE-FTS and SOFIE. Between 30 and 40 km an agreement within 3 % with SCIAMACHY has been found. In the middle stratosphere, there is no clear indication of a MIPAS bias since comparisons with various instruments contradict each other. In the lower stratosphere (below 25 km) MIPAS CH4 is biased high with respect to satellite instruments, and the most likely estimate of this bias is 14 %. However, in the comparison with CH4 data obtained from cryogenic whole-air sampler (cryosampler) measurements, there is no evidence of a high bias in MIPAS between 20 and 25 km altitude. Precision validation is performed on collocated MIPAS–MIPAS pairs and suggests a slight underestimation of its uncertainties by a factor of 1.2. No significant evidence of an instrumental drift has been found.

scholarly journals Analysis of Convective Transport and Parameter Sensitivity in a Single Column Version of the Goddard Earth Observation System, Version 5, General Circulation Model

2009 ◽  
Vol 66 (3) ◽  
pp. 627-646 ◽  
Author(s):  
L. E. Ott ◽  
J. Bacmeister ◽  
S. Pawson ◽  
K. Pickering ◽  
G. Stenchikov ◽  
...  
Keyword(s):  
Mass Flux ◽  
General Circulation ◽  
Parameter Sensitivity ◽  
Convective Transport ◽  
Trace Gas ◽  
Gas Mixing ◽  
Mixing Ratios ◽  
Mass Fluxes ◽  
Single Column ◽  
Convective Mass Flux

Abstract Convection strongly influences the distribution of atmospheric trace gases. General circulation models (GCMs) use convective mass fluxes calculated by parameterizations to transport gases, but the results are difficult to compare with trace gas observations because of differences in scale. The high resolution of cloud-resolving models (CRMs) facilitates direct comparison with aircraft observations. Averaged over a sufficient area, CRM results yield a validated product directly comparable to output from a single global model grid column. This study presents comparisons of vertical profiles of convective mass flux and trace gas mixing ratios derived from CRM and single column model (SCM) simulations of storms observed during three field campaigns. In all three cases, SCM simulations underpredicted convective mass flux relative to CRM simulations. As a result, the SCM simulations produced lower trace gas mixing ratios in the upper troposphere in two of the three storms than did the CRM simulations. The impact of parameter sensitivity in the moist physics schemes employed in the SCM has also been examined. Statistical techniques identified the most significant parameters influencing convective transport. Convective mass fluxes are shown to be strongly dependent on chosen parameter values. Results show that altered parameter settings can substantially improve the comparison between SCM and CRM convective mass flux. Upper tropospheric trace gas mixing ratios were also improved in two storms. In the remaining storm, the SCM representation of CO2 was not improved because of differences in entrainment and detrainment levels in the CRM and SCM simulations.

Trace gases and organic aerosol at a rural site in Vietnam during large scale biomass burning

2021 ◽  
Author(s):  
Simone M. Pieber ◽  
Dac-Loc Nguyen ◽  
Hendryk Czech ◽  
Stephan Henne ◽  
Nicolas Bukowiecki ◽  
...  
Keyword(s):  
Air Quality ◽  
Chemical Composition ◽  
Biomass Burning ◽  
Large Scale ◽  
Trace Gases ◽  
Organic Aerosol ◽  
Trace Gas ◽  
Rural Site ◽  
Air Masses ◽  
Mixing Ratios

<p>Open biomass burning (BB) is a globally widespread phenomenon. The fires release pollutants, which are harmful for human and ecosystem health and alter the Earth's radiative balance. Yet, the impact of various types of BB on the global radiative forcing remains poorly constrained concerning greenhouse gas emissions, BB organic aerosol (OA) chemical composition and related light absorbing properties. Fire emissions composition is influenced by multiple factors (e.g., fuel and thereby vegetation-type, fuel moisture, fire temperature, available oxygen). Due to regional variations in these parameters, studies in different world regions are needed. Here we investigate the influence of seasonally recurring BB on trace gas concentration and air quality at the regional Global Atmosphere Watch (GAW) station Pha Din (PDI) in rural Northwestern Vietnam. PDI is located in a sparsely populated area on the top of a hill (1466 m a.s.l.) and is well suited to study the large-scale fires on the Indochinese Peninsula, whose pollution plumes are frequently transported towards the site [1]. We present continuous trace gas observations of CO<sub>2</sub>, CH<sub>4</sub>, CO, and O<sub>3</sub> conducted at PDI since 2014 and interpret the data with atmospheric transport simulations. Annually recurrent large scale BB leads to hourly time-scale peaks CO mixing ratios at PDI of 1000 to 1500 ppb around every April since the start of data collection in 2014. We complement this analysis with carbonaceous PM<sub>2.5 </sub>chemical composition analyzed during an intensive campaign in March-April 2015. This includes measurements of elemental and organic carbon (EC/OC) and more than 50 organic markers, such as sugars, PAHs, fatty acids and nitro-aromatics [2]. For the intensive campaign, we linked CO, CO<sub>2</sub>, CH<sub>4</sub> and O<sub>3</sub> mixing ratios to a statistical classification of BB events, which is based on OA composition. We found increased CO and O<sub>3</sub> levels during medium and high BB influence during the intensive campaign. A backward trajectory analysis confirmed different source regions for the identified periods based on the OA cluster. Typically, cleaner air masses arrived from northeast, i.e., mainland China and Yellow sea during the intensive campaign. The more polluted periods were characterized by trajectories from southwest, with more continental recirculation of the medium cluster, and more westerly advection for the high cluster. These findings highlight that BB activities in Northern Southeast Asia significantly enhances the regional OA loading, chemical PM<sub>2.5 </sub>composition and the trace gases in northwestern Vietnam. The presented analysis adds valuable data on air quality in a region of scarce data availability.</p><p> </p><p><strong>REFERENCES</strong></p><p>[1] Bukowiecki, N. et al. Effect of Large-scale Biomass Burning on Aerosol Optical Properties at the GAW Regional Station Pha Din, Vietnam. AAQR. 19, 1172–1187 (2019).</p><p>[2] Nguyen, D. L, et al. Carbonaceous aerosol composition in air masses influenced by large-scale biomass burning: a case-study in Northwestern Vietnam. ACPD., https://doi.org/10.5194/acp-2020-1027, in review, 2020.</p>

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