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  • 1
    In: Journal of Geophysical Research, American Geophysical Union (AGU), Vol. 112, No. D5 ( 2007-03-03)
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2007
    detail.hit.zdb_id: 2033040-6
    detail.hit.zdb_id: 3094104-0
    detail.hit.zdb_id: 2130824-X
    detail.hit.zdb_id: 2016813-5
    detail.hit.zdb_id: 2016810-X
    detail.hit.zdb_id: 2403298-0
    detail.hit.zdb_id: 2016800-7
    detail.hit.zdb_id: 161666-3
    detail.hit.zdb_id: 161667-5
    detail.hit.zdb_id: 2969341-X
    detail.hit.zdb_id: 161665-1
    detail.hit.zdb_id: 3094268-8
    detail.hit.zdb_id: 710256-2
    detail.hit.zdb_id: 2016804-4
    detail.hit.zdb_id: 3094181-7
    detail.hit.zdb_id: 3094219-6
    detail.hit.zdb_id: 3094167-2
    detail.hit.zdb_id: 2220777-6
    detail.hit.zdb_id: 3094197-0
    SSG: 16,13
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  • 2
    In: Applied Optics, Optica Publishing Group, Vol. 39, No. 30 ( 2000-10-20), p. 5531-
    Type of Medium: Online Resource
    ISSN: 0003-6935 , 1539-4522
    Language: English
    Publisher: Optica Publishing Group
    Publication Date: 2000
    detail.hit.zdb_id: 207387-0
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  • 3
    Online Resource
    Online Resource
    Copernicus GmbH ; 2018
    In:  Atmospheric Measurement Techniques Vol. 11, No. 8 ( 2018-08-13), p. 4707-4723
    In: Atmospheric Measurement Techniques, Copernicus GmbH, Vol. 11, No. 8 ( 2018-08-13), p. 4707-4723
    Abstract: Abstract. Discrepancies in ozone retrievals in MIPAS channels A (685–970 cm−1) and AB (1020–1170 cm−1) have been a long-standing problem in MIPAS data analysis, amounting to an interchannel bias (AB–A) of up to 8 % between ozone volume mixing ratios in the altitude range 30–40 km. We discuss various candidate explanations, among them forward model and retrieval algorithm errors, interchannel calibration inconsistencies and spectroscopic data inconsistencies. We show that forward-modelling errors as well as errors in the retrieval algorithm can be ruled out as an explanation because the bias can be reproduced with an entirely independent retrieval algorithm (GEOFIT), relying on a different forward radiative transfer model. Instrumental and calibration issues can also be refuted as an explanation because ozone retrievals based on balloon-borne measurements with a different instrument (MIPAS-B) and an independent level-1 data processing scheme produce a rather similar interchannel bias. Thus, spectroscopic inconsistencies in the MIPAS database used for ozone retrieval are practically the only reason left. To further investigate this issue, we performed retrievals using additional spectroscopic databases. Various versions of the HITRAN database generally produced rather similar channel AB–A differences. Use of a different database, namely GEISA-2015, led to similar results in channel AB, but to even higher ozone volume mixing ratios for channel A retrievals, i.e. to a reversal of the bias. We show that the differences in MIPAS channel A retrievals result from about 13 % lower air-broadening coefficients of the strongest lines in the GEISA-2015 database. Since the errors in line intensity of the major lines used in MIPAS channels A and AB are reported to be considerably lower than the observed bias, we posit that a major part of the channel AB–A differences can be attributed to inconsistent air-broadening coefficients as well. To corroborate this assumption we show some clearly inconsistent air-broadening coefficients in the HITRAN-2008 database. The interchannel bias in retrieved ozone amounts can be reduced by increasing the air-broadening coefficients of the lines in MIPAS channel AB in the HITRAN-2008 database by 6 %–8 %.
    Type of Medium: Online Resource
    ISSN: 1867-8548
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2505596-3
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  • 4
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 18, No. 11 ( 2018-06-15), p. 8389-8408
    Abstract: Abstract. We have used satellite observations and a simulation from the TOMCAT chemistry transport model (CTM) to investigate the influence of the well-known wintertime North Atlantic Oscillation (NAO) on European tropospheric composition. Under the positive phase of the NAO (NAO-high), strong westerlies tend to enhance transport of European pollution (e.g. nitrogen oxides, NOx; carbon monoxide, CO) away from anthropogenic source regions. In contrast, during the negative phase of the NAO (NAO-low), more stable meteorological conditions lead to a build-up of pollutants over these regions relative to the wintertime average pollution levels. However, the secondary pollutant ozone shows the opposite signal of larger values during NAO-high. NAO-high introduces Atlantic ozone-enriched air into Europe, while under NAO-low westerly transport of ozone is reduced, yielding lower values over Europe. Furthermore, ozone concentrations are also decreased by chemical loss through the reaction with accumulated primary pollutants such as nitric oxide (NO) in NAO-low. Peroxyacetyl nitrate (PAN) in the upper troposphere–lower stratosphere (UTLS) peaks over Iceland and southern Greenland in NAO-low, between 200 and 100 hPa, consistent with the trapping by an anticyclone at this altitude. Model simulations show that enhanced PAN over Iceland and southern Greenland in NAO-low is associated with vertical transport of polluted air from the mid-troposphere into the UTLS. Overall, this work shows that NAO circulation patterns are an important governing factor for European wintertime composition and air pollution.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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  • 5
    In: Atmospheric Measurement Techniques, Copernicus GmbH, Vol. 14, No. 6 ( 2021-06-07), p. 4111-4138
    Abstract: Abstract. A new global set of atmospheric temperature profiles is retrieved from recalibrated radiance spectra recorded with the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS). Changes with respect to previous data versions include a new radiometric calibration considering the time dependency of the detector nonlinearity and a more robust frequency calibration scheme. Temperature is retrieved using a smoothing constraint, while tangent altitude pointing information is constrained using optimal estimation. ECMWF ERA-Interim is used as a priori temperature below 43 km. Above, a priori data are based on data from the Whole Atmosphere Community Climate Model Version 4 (WACCM4). Bias-corrected fields from specified dynamics runs, sampled at the MIPAS times and locations, are used, blended with ERA-Interim between 43 and 53 km. Horizontal variability of temperature is considered by scaling an a priori 3D temperature field in the orbit plane in a way that the horizontal structure is provided by the a priori while the vertical structure comes from the measurements. Additional microwindows with better sensitivity at higher altitudes are used. The background continuum is jointly fitted with the target parameters up to 58 km altitude. The radiance offset correction is strongly regularized towards an empirically determined vertical offset profile. In order to avoid the propagation of uncertainties of O3 and H2O a priori assumptions, the abundances of these species are retrieved jointly with temperature. The retrieval is based on HITRAN 2016 spectroscopic data, with a few amendments. Temperature-adjusted climatologies of vibrational populations of CO2 states emitting in the 15 µm region are used in the radiative transfer modeling in order to account for non-local thermodynamic equilibrium. Numerical integration in the radiative transfer model is now performed at higher accuracy. The random component of the temperature uncertainty typically varies between 0.4 and 1 K, with occasional excursions up to 1.3 K above 60 km altitude. The leading sources of the random component of the temperature error are measurement noise, gain calibration uncertainty, spectral shift, and uncertain CO2 mixing ratios. The systematic error is caused by uncertainties in spectroscopic data and line shape uncertainties. It ranges from 0.2 K at 20 km altitude for northern midlatitude summer conditions to 2.3 K at 12 km for tropical conditions. The estimated total uncertainty amounts to values between 0.6 K at 20 km for midlatitude summer conditions to 2.5 K at 12–15 km for tropical conditions. The vertical resolution varies around 3 km for altitudes below 50 km. The long-term drift encountered in the previous temperature product has been largely reduced. The consistency between high spectral resolution results from 2002 to 2004 and the reduced spectral resolution results from 2005 to 2012 has been largely improved. As expected, most pronounced temperature differences between version 8 and previous data versions are found in elevated stratopause situations. The fact that the phase of temperature waves seen by MIPAS is not locked to the wave phase found in ECMWF analyses demonstrates that our retrieval provides independent information and does not merely reproduce the prior information.
    Type of Medium: Online Resource
    ISSN: 1867-8548
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2021
    detail.hit.zdb_id: 2505596-3
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  • 6
    Online Resource
    Online Resource
    Copernicus GmbH ; 2019
    In:  Atmospheric Measurement Techniques Vol. 12, No. 9 ( 2019-09-26), p. 5155-5160
    In: Atmospheric Measurement Techniques, Copernicus GmbH, Vol. 12, No. 9 ( 2019-09-26), p. 5155-5160
    Abstract: Abstract. To avoid unnecessary data traffic it is sometimes desirable to apply mean averaging kernels to mean profiles of atmospheric state variables. Unfortunately, application of averaging kernels and averaging are not commutative in cases when averaging kernels and state variables are correlated. That is to say, the application of individual averaging kernels to individual profiles and subsequent averaging will, in general, lead to different results than averaging of the original profiles prior to the application of the mean averaging kernels, unless profiles and averaging kernels are fully independent. The resulting error, however, can be corrected by subtraction of the covariance between the averaging kernel and the vertical profile. Thus, it is recommended to calculate the covariance profile along with the mean profile and the mean averaging kernel.
    Type of Medium: Online Resource
    ISSN: 1867-8548
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2019
    detail.hit.zdb_id: 2505596-3
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  • 7
    Online Resource
    Online Resource
    Copernicus GmbH ; 2022
    In:  Atmospheric Measurement Techniques Vol. 15, No. 23 ( 2022-12-06), p. 6991-7018
    In: Atmospheric Measurement Techniques, Copernicus GmbH, Vol. 15, No. 23 ( 2022-12-06), p. 6991-7018
    Abstract: Abstract. This paper describes the error estimation for temperature and trace gas mixing ratios retrieved from the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) limb emission spectra. The following error sources are taken into account: measurement noise, propagated temperature and pointing noise, uncertainties in the abundances of spectrally interfering species, instrument line shape errors, and spectroscopic data uncertainties in terms of line intensities and broadening coefficients. Furthermore, both the direct impact of volatile and persistent gain calibration uncertainties, offset calibration, and spectral calibration uncertainties, as well as their impact through propagated calibration-related temperature and pointing uncertainties, are considered. An error source specific to the MIPAS upper atmospheric observation mode is the propagation of the smoothing error crosstalk of the combined NO and temperature retrieval. Whenever non-local thermodynamic equilibrium modelling is used in the retrieval, related kinetic constants and mixing ratios of species involved in the modelling of populations of excitational states also contribute to the error budget. Both generalized Gaussian error propagation and perturbation studies are used to estimate the error components. Error correlations are taken into account. Estimated uncertainties are provided for a multitude of atmospheric conditions. Some error sources were found to contribute both to the random and the systematic component of the total estimated error. The sequential nature of the MIPAS retrievals gives rise to entangled errors. These are caused by error sources that affect the uncertainty in the final data product via multiple pathways, i.e., on the one hand, directly, and, on the other hand, via errors caused in a preceding retrieval step. These errors tend to partly compensate for each other. The hard-to-quantify effect of the horizontally non-homogeneous atmosphere and unknown error correlations of spectroscopic data are considered to be the major limitations of the MIPAS error estimation.
    Type of Medium: Online Resource
    ISSN: 1867-8548
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2022
    detail.hit.zdb_id: 2505596-3
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  • 8
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 22, No. 5 ( 2022-03-17), p. 3675-3691
    Abstract: Abstract. In this study, we present simultaneous airborne measurements of peroxyacetyl nitrate (PAN), ethane (C2H6), formic acid (HCOOH), methanol (CH3OH), and ethylene (C2H4) above the South Atlantic in September and October 2019. Observations were obtained from the Gimballed Limb Observer for Radiance Imaging of the Atmosphere (GLORIA), as two-dimensional altitude cross sections along the flight path. The flights were part of the SouthTRAC (Transport and Composition in the Southern Hemisphere Upper Troposphere/Lower Stratosphere) campaign with the German High Altitude and Long Range Research Aircraft (HALO). On two flights (8 September 2019 and 7 October 2019), large enhancements of all these substances were found between 7 and 14 km altitude with maximum volume mixing ratios (VMRs) of 1000 pptv for PAN, 1400 pptv for C2H6, 800 pptv for HCOOH, 4500 pptv for CH3OH, and 200 pptv for C2H4. One flight showed a common filamentary structure in the trace gas distributions, while the second flight is characterized by one large plume. Using backward trajectories, we show that measured pollutants likely reached upper troposphere and lower stratosphere (UTLS) altitudes above South America and central Africa, where elevated PAN VMRs are visible at the surface layer of the Copernicus Atmosphere Monitoring Service (CAMS) model during the weeks before both measurements. In comparison to results of the CAMS reanalysis interpolated onto the GLORIA measurement geolocations, we show that the model is able to reproduce the overall structure of the measured pollution trace gas distributions. For PAN, the absolute VMRs are in agreement with the GLORIA measurements. However, C2H6 and HCOOH are generally underestimated by the model, while CH3OH and C2H4, the species with the shortest atmospheric lifetimes of the pollution trace gases discussed, are overestimated by CAMS. The good agreement between model and observations for PAN suggests that the general transport pathways and emissions locations are well captured by the model. The poorer agreement for other species is therefore most likely linked to model deficiencies in the representation of loss processes and emission strength.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2022
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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  • 9
    In: Journal of Quantitative Spectroscopy and Radiative Transfer, Elsevier BV, Vol. 72, No. 3 ( 2002-2), p. 249-280
    Type of Medium: Online Resource
    ISSN: 0022-4073
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2002
    detail.hit.zdb_id: 1491916-3
    SSG: 11
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  • 10
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 18, No. 2 ( 2018-01-19), p. 691-703
    Abstract: Abstract. It is known from ground-based measurements made during the 1982–1983 and 1997–1998 El Niño events that atmospheric hydrogen cyanide (HCN) tends to be higher during such years than at other times. The Microwave Limb Sounder (MLS) on the Aura satellite has been measuring HCN mixing ratios since launch in 2004; the measurements are ongoing at the time of writing. The winter of 2015–2016 saw the largest El Niño event since 1997–1998. We present MLS measurements of HCN in the lower stratosphere for the Aura mission to date, comparing the 2015–2016 El Niño period to the rest of the mission. HCN in 2015–2016 is higher than at any other time during the mission, but ground-based measurements suggest that it may have been even more elevated in 1997–1998. As the MLS HCN data are essentially unvalidated, we show them alongside data from the MIPAS and ACE-FTS instruments; the three instruments agree reasonably well in the tropical lower stratosphere. Global HCN emissions calculated from the Global Fire Emissions Database (GFED v4.1) database are much greater during large El Niño events and are greater in 1997–1998 than in 2015–2016, thereby showing good qualitative agreement with the measurements. Correlation between El Niño–Southern Oscillation (ENSO) indices, measured HCN, and GFED HCN emissions is less clear if the 2015–2016 event is excluded. In particular, the 2009–2010 winter had fairly strong El Niño conditions and fairly large GFED HCN emissions, but very little effect is observed in the MLS HCN.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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