459 research outputs found
Measurement of HO2 and other trace gases in the stratosphere using a high resolution far-infrared spectrometer at 28 KM
The major events and results to date of the ongoing program of measuring stratospheric composition by the technique of far-infrared Fourier-transform spectroscopy from a balloon-borne platform are reviewed. The highlights of this period were the two balloon flight campaigns which were performed at Palestine, Texas, both of which produced large amounts of scientifically useful data
Retrieval and molecule sensitivity studies for the global ozone monitoring experiment and the scanning imaging absorption spectrometer for atmospheric chartography
The Global Ozone Monitoring Experiment (GOME) and the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) are diode based spectrometers that will make atmospheric constituent and aerosol measurements from European satellite platforms beginning in the mid 1990's. GOME measures the atmosphere in the UV and visible in nadir scanning, while SCIAMACHY performs a combination of nadir, limb, and occultation measurements in the UV, visible, and infrared. A summary is presented of the sensitivity studies that were performed for SCIAMACHY measurements. As the GOME measurement capability is a subset of the SCIAMACHY measurement capability, the nadir, UV, and visible portion of the studies is shown to apply to GOME as well
Measurement of HO2 and Other Trace Gases in the Stratosphere using a High Resolution Far-Infrared Spectrometer
This report is a continuation of the analysis of data from past flights, exploring issues such as radical partitioning, stratospheric transport, and the ozone budget
Seasonal and interannual variability of North American isoprene emissions as determined by formaldehyde column measurements from space
Formaldehyde (HCHO) columns measured from space by solar UV backscatter allow mapping of reactive hydrocarbon emissions. The principal contributor to these emissions during the growing season is the biogenic hydrocarbon isoprene, which is of great importance for driving regional and global tropospheric chemistry. We present seven years (1995-2001) of HCHO column data for North America from the Global Ozone Monitoring Experiment (GOME), and show that the general seasonal and interannual variability of these data is consistent with knowledge of isoprene emission. There are some significant regional discrepancies with the seasonal patterns predicted from current isoprene emission models, and we suggest that these may reflect flaws in the models. The interannual variability of HCHO columns observed by GOME appears to follow the interannual variability of surface temperature, as expected from current isoprene emission models
Characterization of the OCO-2 instrument line shape functions using on-orbit solar measurements
Accurately characterizing the instrument line shape (ILS) of the Orbiting Carbon Observatory-2 (OCO-2) is challenging and highly important due to its high spectral resolution and requirement for retrieval accuracy (0. 25 %) compared to previous spaceborne grating spectrometers. On-orbit ILS functions for all three bands of the OCO-2 instrument have been derived using its frequent solar measurements and high-resolution solar reference spectra. The solar reference spectrum generated from the 2016 version of the Total Carbon Column Observing Network (TCCON) solar line list shows significant improvements in the fitting residual compared to the solar reference spectrum currently used in the version 7 Level 2 algorithm in the O₂ A band. The analytical functions used to represent the ILS of previous grating spectrometers are found to be inadequate for the OCO-2 ILS. Particularly, the hybrid Gaussian and super-Gaussian functions may introduce spurious variations, up to 5 % of the ILS width, depending on the spectral sampling position, when there is a spectral undersampling. Fitting a homogeneous stretch of the preflight ILS together with the relative widening of the wings of the ILS is insensitive to the sampling grid position and accurately captures the variation of ILS in the O₂ A band between decontamination events. These temporal changes of ILS may explain the spurious signals observed in the solar-induced fluorescence retrieval in barren areas
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Improved Algorithm for MODIS Satellite Retrievals of Aerosol Optical Depths Over Western North America
Quantitative evaluation of chemical transport models (CTMs) with aerosol optical depth (AOD) products retrieved from satellite backscattered reflectances can be compromised by inconsistent assumptions of aerosol optical properties and errors in surface reflectance estimates. We present an improved AOD retrieval algorithm for the MODIS satellite instrument using locally derived surface reflectances and CTM aerosol optical properties for the 0.47, 0.65, and 2.13 μm MODIS channels. Assuming negligible atmospheric reflectance at 2.13 μm in cloud-free conditions, we derive 0.65/2.13 surface reflectance ratios at 1° × 1.25° horizontal resolution for the continental United States in summer 2004 from the subset of top-of-atmosphere (TOA) reflectance data with minimal aerosol reflectance. We obtain a mean ratio of 0.57 ± 0.10 for the continental United States, with high values over arid regions and low values over the Midwest prairies. The higher surface reflectance ratios explain the high AOD bias over arid regions found in previous MODIS retrievals. We calculate TOA reflectances for each MODIS scene using local aerosol optical properties from the GEOS-Chem CTM, and fit these reflectances to the observed MODIS TOA reflectances for a best estimate of AODs for that scene. Comparison with coincident ground-based (AERONET) AOD observations at 16 sites in the western and central United States in summer 2004 shows poor correlation in the daily data but the correlation improves as averaging time increases. Averaging over the available coincident observations (n = 11–44 days) results in strong correlations (R0.47μm = 0.90, R0.65μm = 0.67) and a 19% low bias, representing considerable improvement over the operational MODIS AOD products in this region.Earth and Planetary SciencesEngineering and Applied Science
Tunable far infrared studies of molecular parameters in support of stratospheric measurements
Lab studies were made in support of far infrared spectroscopy of the stratosphere using the Tunable Far InfraRed (TuFIR) method of ultrahigh resolution spectroscopy and, more recently, spectroscopic and retrieval calculations performed in support of satellite-based atmospheric measurement programs: the Global Ozone Monitoring Experiment (GOME), and the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY)
Air mass factor formulation for spectroscopic measurements from satellites: Application to formaldehyde retrievals from the Global Ozone Monitoring Experiment
Abstract. We present a new formulation for the air mass factor (AMF) to convert slant column measurements of optically thin atmospheric species from space into total vertical columns. Because of atmospheric scattering, the AMF depends on the vertical distribution of the species. We formulate the AMF as the integral of the relative vertical distribution (shape factor) of the species over the depth of the atmosphere, weighted by altitudedependent coefficients (scattering weights) computed independently from a radiative transfer model. The scattering weights are readily tabulated, and one can then obtain the AMF for any observation scene by using shape factors from a three dimensional (3-D) atmospheric chemistry model for the period of observation. This approach subsequently allows objective evaluation of the 3-D model with the observed vertical columns, since the shape factor and the vertical column in the model represent two independent pieces of information. We demonstrate the AMF method by using slant column measurements of formaldehyde at 346 nm from the Global Ozone Monitoring Experiment satellite instrument over North America during July 1996. Shape factors are computed with the Global Earth Observing System CHEMistry (GEOS-CHEM) global 3-D model and are checked for consistency with the few available aircraft measurements. Scattering weights increase by an order of magnitude from the surface to the upper troposphere. The AMFs are typically 20-40 % less over continents than over the oceans and are approximately half the values calculated in the absence of scattering. Model-induced errors in the AMF are estimated to be • 10%. The GEOS-CHEM model captures 50 % and 60 % of the variances in the observed slant and vertical columns, respectively. Comparison of the simulated and observed vertical columns allows assessment of model bias. 1
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