Spectroscopic challenges in direct problems of the satellite atmospheric sounding and ways of their resolving

2016 ◽  
Vol 29 (9) ◽  
Keyword(s):  
Atmospheric Sounding ◽  
Direct Problems

scholarly journals The vertical distribution of volcanic SO<sub>2</sub> plumes measured by IASI

2016 ◽  
Vol 16 (7) ◽  
pp. 4343-4367 ◽  
Author(s):  
Elisa Carboni ◽  
Roy G. Grainger ◽  
Tamsin A. Mather ◽  
David M. Pyle ◽  
Gareth E. Thomas ◽  
...  
Keyword(s):  
Volcanic Eruptions ◽  
Maximum Amount ◽  
The Other ◽  
High Spectral Resolution ◽  
Explosive Eruptions ◽  
Atmospheric Processes ◽  
Atmospheric Sounding ◽  
Volcanic Emission ◽  
The Vertical Distribution ◽  
Atmospheric Constituent

Abstract. Sulfur dioxide (SO2) is an important atmospheric constituent that plays a crucial role in many atmospheric processes. Volcanic eruptions are a significant source of atmospheric SO2 and its effects and lifetime depend on the SO2 injection altitude. The Infrared Atmospheric Sounding Interferometer (IASI) on the METOP satellite can be used to study volcanic emission of SO2 using high-spectral resolution measurements from 1000 to 1200 and from 1300 to 1410 cm−1 (the 7.3 and 8.7 µm SO2 bands) returning both SO2 amount and altitude data. The scheme described in Carboni et al. (2012) has been applied to measure volcanic SO2 amount and altitude for 14 explosive eruptions from 2008 to 2012. The work includes a comparison with the following independent measurements: (i) the SO2 column amounts from the 2010 Eyjafjallajökull plumes have been compared with Brewer ground measurements over Europe; (ii) the SO2 plumes heights, for the 2010 Eyjafjallajökull and 2011 Grimsvötn eruptions, have been compared with CALIPSO backscatter profiles. The results of the comparisons show that IASI SO2 measurements are not affected by underlying cloud and are consistent (within the retrieved errors) with the other measurements. The series of analysed eruptions (2008 to 2012) show that the biggest emitter of volcanic SO2 was Nabro, followed by Kasatochi and Grímsvötn. Our observations also show a tendency for volcanic SO2 to reach the level of the tropopause during many of the moderately explosive eruptions observed. For the eruptions observed, this tendency was independent of the maximum amount of SO2 (e.g. 0.2 Tg for Dalafilla compared with 1.6 Tg for Nabro) and of the volcanic explosive index (between 3 and 5).

scholarly journals Stratospheric aerosol radiative forcing simulated by the chemistry climate model EMAC using Aerosol CCI satellite data

2018 ◽  
Vol 18 (17) ◽  
pp. 12845-12857 ◽  
Author(s):  
Christoph Brühl ◽  
Jennifer Schallock ◽  
Klaus Klingmüller ◽  
Charles Robert ◽  
Christine Bingen ◽  
...  
Keyword(s):  
Optical Depth ◽  
Radiative Forcing ◽  
Volcanic Eruptions ◽  
Stratospheric Aerosol ◽  
Radiative Heating ◽  
Aerosol Radiative Forcing ◽  
Tropospheric Aerosol ◽  
Model Aerosol ◽  
Atmospheric Sounding ◽  
Aerosol Radiative

Abstract. This paper presents decadal simulations of stratospheric and tropospheric aerosol and its radiative effects by the chemistry general circulation model EMAC constrained with satellite observations in the framework of the ESA Aerosol CCI project such as GOMOS (Global Ozone Monitoring by Occultation of Stars) and (A)ATSR ((Advanced) Along Track Scanning Radiometer) on the ENVISAT (European Environmental Satellite), IASI (Infrared Atmospheric Sounding Interferometer) on MetOp (Meteorological Operational Satellite), and, additionally, OSIRIS (Optical Spectrograph and InfraRed Imaging System). In contrast to most other studies, the extinctions and optical depths from the model are compared to the observations at the original wavelengths of the satellite instruments covering the range from the UV (ultraviolet) to terrestrial IR (infrared). This avoids conversion artifacts and provides additional constraints for model aerosol and interpretation of the observations. MIPAS (Michelson Interferometer for Passive Atmospheric Sounding) SO2 limb measurements are used to identify plumes of more than 200 volcanic eruptions. These three-dimensional SO2 plumes are added to the model SO2 at the eruption times. The interannual variability in aerosol extinction in the lower stratosphere, and of stratospheric aerosol radiative forcing at the tropopause, is dominated by the volcanoes. To explain the seasonal cycle of the GOMOS and OSIRIS observations, desert dust simulated by a new approach and transported to the lowermost stratosphere by the Asian summer monsoon and tropical convection turns out to be essential. This also applies to the radiative heating by aerosol in the lowermost stratosphere. The existence of wet dust aerosol in the lowermost stratosphere is indicated by the patterns of the wavelength dependence of extinction in observations and simulations. Additional comparison with (A)ATSR total aerosol optical depth at different wavelengths and IASI dust optical depth demonstrates that the model is able to represent stratospheric as well as tropospheric aerosol consistently.

scholarly journals Measurements of hydrogen cyanide (HCN) and acetylene (C<sub>2</sub>H<sub>2</sub>) from the Infrared Atmospheric Sounding Interferometer (IASI)

2013 ◽  
Vol 6 (4) ◽  
pp. 917-925 ◽  
Author(s):  
V. Duflot ◽  
D. Hurtmans ◽  
L. Clarisse ◽  
Y. R'honi ◽  
C. Vigouroux ◽  
...  
Keyword(s):  
Fourier Transform ◽  
Hydrogen Cyanide ◽  
Atmospheric Transport ◽  
Trace Gases ◽  
First Order ◽  
Line Mixing ◽  
Atmospheric Sounding ◽  
First Time ◽  
Order Comparison ◽  
Emission Ratios

Abstract. Hydrogen cyanide (HCN) and acetylene (C2H2) are ubiquitous atmospheric trace gases with medium lifetime, which are frequently used as indicators of combustion sources and as tracers for atmospheric transport and chemistry. Because of their weak infrared absorption, overlapped by the CO2 Q branch near 720 cm−1, nadir sounders have up to now failed to measure these gases routinely. Taking into account CO2 line mixing, we provide for the first time extensive measurements of HCN and C2H2 total columns at Reunion Island (21° S, 55° E) and Jungfraujoch (46° N, 8° E) in 2009–2010 using observations from the Infrared Atmospheric Sounding Interferometer (IASI). A first order comparison with local ground-based Fourier transform infraRed (FTIR) measurements has been carried out allowing tests of seasonal consistency which is reasonably captured, except for HCN at Jungfraujoch. The IASI data shows a greater tendency to high C2H2 values. We also examine a nonspecific biomass burning plume over austral Africa and show that the emission ratios with respect to CO agree with previously reported values.

scholarly journals Measurements of total and tropospheric ozone from IASI: comparison with correlative satellite, ground-based and ozonesonde observations

2009 ◽  
Vol 9 (16) ◽  
pp. 6255-6271 ◽  
Author(s):  
A. Boynard ◽  
C. Clerbaux ◽  
P.-F. Coheur ◽  
D. Hurtmans ◽  
S. Turquety ◽  
...  
Keyword(s):  
Spectral Resolution ◽  
Tropospheric Ozone ◽  
Total Ozone ◽  
Correlation Coefficients ◽  
Positive Bias ◽  
Ozone Concentrations ◽  
Infrared Radiance ◽  
Atmospheric Sounding ◽  
Ozone Monitoring ◽  
Good Agreement

Abstract. In this paper, we present measurements of total and tropospheric ozone, retrieved from infrared radiance spectra recorded by the Infrared Atmospheric Sounding Interferometer (IASI), which was launched on board the MetOp-A European satellite in October 2006. We compare IASI total ozone columns to Global Ozone Monitoring Experiment-2 (GOME-2) observations and ground-based measurements from the Dobson and Brewer network for one full year of observations (2008). The IASI total ozone columns are shown to be in good agreement with both GOME-2 and ground-based data, with correlation coefficients of about 0.9 and 0.85, respectively. On average, IASI ozone retrievals exhibit a positive bias of about 9 DU (3.3%) compared to both GOME-2 and ground-based measurements. In addition to total ozone columns, the good spectral resolution of IASI enables the retrieval of tropospheric ozone concentrations. Comparisons of IASI tropospheric columns to 490 collocated ozone soundings available from several stations around the globe have been performed for the period of June 2007–August 2008. IASI tropospheric ozone columns compare well with sonde observations, with correlation coefficients of 0.95 and 0.77 for the [surface–6 km] and [surface–12 km] partial columns, respectively. IASI retrievals tend to overestimate the tropospheric ozone columns in comparison with ozonesonde measurements. Positive average biases of 0.15 DU (1.2%) and 3 DU (11%) are found for the [surface–6 km] and for the [surface–12 km] partial columns respectively.

scholarly journals An “island” in the stratosphere – on the enhanced annual variation of water vapour in the middle and upper stratosphere in the southern tropics and subtropics

2017 ◽  
Vol 17 (18) ◽  
pp. 11521-11539 ◽  
Author(s):  
Stefan Lossow ◽  
Hella Garny ◽  
Patrick Jöckel
Keyword(s):  
Water Vapour ◽  
Atmospheric Chemistry ◽  
Annual Variation ◽  
Trace Gases ◽  
Michelson Interferometer ◽  
Full Account ◽  
Weather Forecasts ◽  
European Centre ◽  
Atmospheric Sounding ◽  
Medium Range

Abstract. The amplitude of the annual variation in water vapour exhibits a distinct isolated maximum in the middle and upper stratosphere in the southern tropics and subtropics, peaking typically around 15° S in latitude and close to 3 hPa (∼  40.5 km) in altitude. This enhanced annual variation is primarily related to the Brewer–Dobson circulation and hence also visible in other trace gases. So far this feature has not gained much attention in the literature and the present work aims to add more prominence. Using Envisat/MIPAS (Environmental Satellite/Michelson Interferometer for Passive Atmospheric Sounding) observations and ECHAM/MESSy (European Centre for Medium-Range Weather Forecasts Hamburg/Modular Earth Submodel System) Atmospheric Chemistry (EMAC) simulations we provide a dedicated illustration and a full account of the reasons for this enhanced annual variation.

scholarly journals Vertical level selection for temperature and trace gas profile retrievals using IASI

2015 ◽  
Vol 8 (6) ◽  
pp. 2359-2369 ◽  
Author(s):  
R. A. Vincent ◽  
A Dudhia ◽  
L. J. Ventress
Keyword(s):  
Trace Gas ◽  
Radiative Transfer Model ◽  
Transfer Model ◽  
Infrared Observation ◽  
Atmospheric Sounding ◽  
Selection For ◽  
Vertical Spacing ◽  
Vertical Level ◽  
New Iterative Method ◽  
Grid Based

Abstract. This work presents a new iterative method for optimally selecting a vertical retrieval grid based on the location of the information while accounting for inter-level correlations. Sample atmospheres initially created to parametrise the Radiative Transfer Model for the Television Infrared Observation Satellite Operational Vertical Sounder (RTTOV) forward model are used to compare the presented iterative selection method with two other common approaches, which are using levels of equal vertical spacing and selecting levels based on the cumulative trace of the averaging kernel matrix (AKM). This new method is shown to outperform compared methods for simulated profile retrievals of temperature, H2O, O3, CH4, and CO with the Infrared Atmospheric Sounding Interferometer (IASI). However, the benefits of using the more complicated iterative approach compared to the simpler cumulative trace method are slight and may not justify the added effort for the cases studied, but may be useful in other scenarios where temperature and trace gases have strong vertical gradients with significant estimate sensitivity. Furthermore, comparing retrievals using a globally optimised static grid vs. a locally adapted one shows that a static grid performs nearly as well for retrievals of O3, CH4, and CO. However, developers of temperature and H2O retrieval schemes may at least consider using adaptive or location specific vertical retrieval grids.

scholarly journals Instantaneous longwave radiative impact of ozone: an application on IASI/MetOp observations

2015 ◽  
Vol 15 (15) ◽  
pp. 21177-21218
Author(s):  
S. Doniki ◽  
D. Hurtmans ◽  
L. Clarisse ◽  
C. Clerbaux ◽  
H. M. Worden ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
Climate Model ◽  
Longwave Radiation ◽  
Polar Regions ◽  
Direct Integration ◽  
Direct Integration Method ◽  
Radiative Impact ◽  
Ozone Variation ◽  
Atmospheric Sounding ◽  
Stratospheric Intrusions

Abstract. Ozone is an important greenhouse gas in terms of anthropogenic radiative forcing (RF). RF calculations for ozone were until recently entirely model based and significant discrepancies were reported due to different model characteristics. However, new instantaneous radiative kernels (IRKs) calculated from hyperspectral thermal IR satellites have been able to help adjudicate between different climate model RF calculations. IRKs are defined as the sensitivity of the outgoing longwave radiation (OLR) flux with respect to the ozone vertical distribution in the full 9.6 μm band. Previous methods applied to measurements from the Tropospheric Emission Spectrometer (TES) on Aura, rely on an anisotropy approximation for the angular integration. In this paper, we present a more accurate but more computationally expensive method to calculate these kernels. The method of direct integration is based on similar principles with the anisotropy approximation, but deals more precisely with the integration of the Jacobians. We describe both methods and highlight their differences with respect to the IRKs and the ozone longwave radiative effect (LWRE), i.e. the radiative impact in OLR due to absorption by ozone, for both tropospheric and total columns, from measurements of the Infrared Atmospheric Sounding Interferometer (IASI) onboard MetOp-A. Biases between the two methods vary from −25 to +20 % for the LWRE, depending on the viewing angle. These biases point to the inadequacy of the anisotropy method, especially at nadir, suggesting that the TES derived LWRE are biased low by around 25 % and that chemistry-climate model OLR biases with respect to TES are underestimated. In this paper we also exploit the sampling performance of IASI to obtain first daily global distributions of the LWRE, for 12 days (the 15th of each month) in 2011, calculated with the direct integration method. We show that the temporal variation of global and latitudinal averages of the LWRE shows patterns which are controlled by changes in the surface temperature and ozone variation due to specific processes, such as the ozone hole in the Polar regions and stratospheric intrusions into the troposphere.

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