[1] Retrieval of abundances of atmospheric species from limb infrared emission spectra requires accurate knowledge of the pointing of the instrument in terms of elevation, as well as temperature and pressure profiles. An optimal estimation-based method is presented to infer these quantities from measured spectra. The successful and efficient joint retrieval of these largely correlated quantities depends strongly on the proper selection of the retrieval space, the selection of spectral microwindows, and the choice of reasonable constraints which force the solution to be stable. The proposed strategy was applied to limb emission spectra recorded with the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on board the Envisat research satellite in order to validate the instrument pointing information based on the satellite's orbit and attitude control system which uses star tracker information as a reference. Both systematic and periodic pointing calibration errors were detected, which meanwhile have been corrected to a major part. Furthermore, occasional pitch jumps were detected, which could be assigned to parameter uploads to the satellite's orbit and attitude control system. It has been shown that in general, it is justified to assume local thermodynamic equilibrium below 60 km for these purposes. The retrieval method presented has been proven to be suitable for independent monitoring of MIPAS line-of-sight pointing.
Abstract.A comprehensive calibration procedure for mobile, low-resolution, solar-absorption FTIR spectrometers, used for greenhouse gases observations, is developed. These instruments commend themselves for campaign use and deployment at remote sites. The instrumental line shape (ILS) of each spectrometer has been thoroughly characterized by analyzing the shape of H 2 O signatures in open path spectra. A setup for the external source is suggested and the invariance of derived ILS parameters with regard to chosen path length is demonstrated. The instrumental line shape characteristics of all spectrometers were found to be close to nominal. Side-by-side solar observations before and after a campaign, which involved shipping of all spectrometers to a selected target site and back, are applied for verifying the temporal invariability of instrumental characteristics and for deriving intercalibration factors for XCO 2 and XCH 4 , which take into account residual differences of instrumental characteristics. An excellent level of agreement and stability was found between the different spectrometers: the uncorrected biases in XCO 2 and XCH 4 are smaller than 0.01 and 0.15 %, respectively, and the drifts are smaller than 0.005 and 0.035 %. As an additional sensitive demonstration of the instrumental performance we show the excellent agreement of ground pressure values obtained from the total column measurements of O 2 and barometric records. We find a calibration factor of 0.9700 for the spectroscopic measurements in comparison to the barometric records and a very small scatter between the individual spectrometers (0.02 %). As a final calibration step, using a co-located TCCON (Total Carbon Column Observation Network) spectrometer as a reference, a common scaling factor has been derived for the XCO 2 and XCH 4 products, which ensures that the records are traceable to the WMO in situ scale.
Abstract. Five portable Bruker EM27/SUN FTIR (Fourier transform infrared) spectrometers have been used for the accurate and precise observation of column-averaged abundances of CO2 and CH4 around the major city Berlin. In the work by Frey et al. (2015), a calibration procedure is developed and applied to the set of spectrometers used for the Berlin campaign. Here, we describe the observational setup of the campaign and aspects of the data analysis, and we present the recorded time series of XCH4 and XCO2. We demonstrate that the CO2 emissions of Berlin can be clearly identified in the observations. A simple dispersion model is applied which indicates a total strength of the Berlin source of about 0.8 t CO2 s−1. In the Supplement of this work, we provide the measured data set and auxiliary data. We hope that the model community will exploit this unique data set for state-of-the art inversion studies of CO2 and CH4 sources in the Berlin area.
Abstract. In the lower/middle troposphere, {H 2 O,δD} pairs are good proxies for moisture pathways; however, their observation, in particular when using remote sensing techniques, is challenging. The project MUSICA (MUltiplatform remote Sensing of Isotopologues for investigating the Cycle of Atmospheric water) addresses this challenge by integrating the remote sensing with in situ measurement techniques. The aim is to retrieve calibrated tropospheric {H 2 O,δD} pairs from the middle infrared spectra measured from ground by FTIR (Fourier transform infrared) spectrometers of the NDACC (Network for the Detection of Atmospheric Composition Change) and the thermal nadir spectra measured by IASI (Infrared Atmospheric Sounding Interferometer) aboard the MetOp satellites. In this paper, we present the final MUSICA products, and discuss the characteristics and potential of the NDACC/FTIR and MetOp/IASI {H 2 O,δD} data pairs.First, we briefly resume the particularities of an {H 2 O,δD} pair retrieval. Second, we show that the remote sensing data of the final product version are absolutely calibrated with respect to H 2 O and δD in situ profile references measured in the subtropics, between 0 and 7 km. Third, we reveal that the {H 2 O,δD} pair distributions obtained from the different remote sensors are consistent and allow distinct lower/middle tropospheric moisture pathways to be identified in agreement with multi-year in situ references. Fourth, we document the possibilities of the NDACC/FTIR instruments for climatological studies (due to long-term monitoring) and of the MetOp/IASI sensors for observing diurnal signals on a quasi-global scale and with high horizontal resolution. Fifth, we discuss the risk of misinterpreting {H 2 O,δD} pair distributions due to incomplete processing of the remote sensing products.
The large solar storm in October–November 2003 produced enormous amounts of high‐energy protons which reached the Earth and penetrated into the middle atmosphere in the polar regions. At this time, the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on board the Environmental Satellite (ENVISAT) was observing the atmosphere in the 6–68 km altitude range. MIPAS observed significant enhancements of the NOy components HNO3, N2O5, and ClONO2 in the northern polar stratosphere after the intense solar proton events. Two distinct HNO3 enhancements were observed. An instantaneous increase of 1–2 ppbv was observed immediately after the SPEs and is attributed to gas‐phase chemistry: NO2 + OH + M → HNO3 + M, accelerated by SPE‐produced excess OH. A very large second increase of 1–5 ppbv started around 10 November and lasted until the end of December. It is attributed to NOx (NO + NO2) produced in the mesosphere during the major SPEs in late October/early November and then transported downward during November and December, partially converted to N2O5 in the upper stratosphere, which finally formed HNO3 via ion cluster reactions. N2O5 was observed to increase by 0.1–0.4 ppbv 1–3 days after the major SPEs and reached down to 30 km altitude. A second, more pronounced N2O5 enhancement of up to 1.2 ppbv at 40 km appeared about 12–13 days after the major SPEs. With a delay of 1–2 days after the major SPEs ClONO2 increased by up to 0.4 ppbv (40%) at 32 km altitude. NOy enhancements in the Southern Hemisphere were generally less pronounced.
Editor’s note: For easy download the posted pdf of the State of the Climate for 2019 is a low-resolution file. A high-resolution copy of the report is available by clicking here. Please be patient as it may take a few minutes for the high-resolution file to download.
In a 3.5-year long study, the long-term performance of a mobile, solar absorption Bruker EM27/SUN spectrometer, used for greenhouse gas observations, is checked with respect to a co-located reference Bruker IFS 125HR spectrometer, which is part of the Total Carbon Column Observing Network (TCCON). We find that the EM27/SUN is stable on timescales of several years; the drift per year between the EM27/SUN and the official TCCON product is 0.02 ppmv for XCO 2 and 0.9 ppbv for XCH 4 , which is within the 1σ precision of the comparison, 0.6 ppmv for XCO 2 and 4.3 ppbv for XCH 4 . The bias between the two data sets is 3.9 ppmv for XCO 2 and 13.0 ppbv for XCH 4 . In order to avoid sensitivity-dependent artifacts, the EM27/SUN is also compared to a truncated IFS 125HR data set derived from full-resolution TCCON interferograms. The drift is 0.02 ppmv for XCO 2 and 0.2 ppbv for XCH 4 per year, with 1σ precisions of 0.4 ppmv for XCO 2 and 1.4 ppbv for XCH 4 , respectively. The bias between the two data sets is 0.6 ppmv for XCO 2 and 0.5 ppbv for XCH 4 . With the presented long-term stability, the EM27/SUN qualifies as an useful supplement to the existing TCCON network in remote areas. To achieve consistent performance, such an extension requires careful testing of any spectrometers involved by application of common quality assurance measures. One major aim of the COllaborative Carbon Column Observing Network (COCCON) infrastructure is to provide these services to all EM27/SUN operators. In the framework of COC-CON development, the performance of an ensemble of 30 EM27/SUN spectrometers was tested and found to be very uniform, enhanced by the centralized inspection performed at the Karlsruhe Institute of Technology prior to deployment. Taking into account measured instrumental line shape parameters for each spectrometer, the resulting average bias across the ensemble with respect to the reference EM27/SUN used in the long-term study in XCO 2 is 0.20 ppmv, while it is 0.8 ppbv for XCH 4 . The average standard deviation of the ensemble is 0.13 ppmv for XCO 2 and 0.6 ppbv for XCH 4 . In addition to the robust metric based on absolute differences, we calculate the standard deviation among the empirical calibration factors. The resulting 2σ uncertainty is 0.6 ppmv for XCO 2 and 2.2 ppbv for XCH 4 . As indicated by the executed long-term study on one device presented here, the remaining empirical calibration factor deduced for each individual instrument can be assumed constant over time. Therefore the application of these empirical factors is expected to further improve the EM27/SUN network conformity beyond the scatter among the empirical calibration factors reported above.
Editor’s note: For easy download the posted pdf of the State of the Climate for 2017 is a low-resolution file. A high-resolution copy of the report is available by clicking here. Please be patient as it may take a few minutes for the high-resolution file to download.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.