Isoprene is the atmosphere's most important non-methane organic compound, with key impacts on atmospheric oxidation, ozone, and organic aerosols. In-situ isoprene measurements are sparse, and ...satellite-based constraints have employed an indirect approach using its oxidation product formaldehyde, which is affected by non-isoprene sources plus uncertainty and spatial smearing in the isoprene-formaldehyde relationship. Direct global isoprene measurements are therefore needed to better understand its sources, sinks, and atmospheric impacts. Here we show that the isoprene spectral signatures are detectable from space using the satellite-borne Cross-track Infrared Sounder (CrIS), develop a full-physics retrieval methodology for quantifying isoprene abundances from these spectral features, and apply the algorithm to CrIS measurements over Amazonia. The results are consistent with model output and in-situ data, and establish the feasibility of direct global space-based isoprene measurements. Finally, we demonstrate the potential for combining space-based measurements of isoprene and formaldehyde to constrain atmospheric oxidation over isoprene source regions.
The Orbiting Carbon Observatory-2 (OCO-2) carries and points a three-channel imaging grating spectrometer designed to collect high-resolution, co-boresighted spectra of reflected sunlight within the ...molecular oxygen (O2) A-band at 0.765 microns and the carbon dioxide (CO2) bands at 1.61 and 2.06 microns. These measurements are calibrated and then combined into soundings that are analyzed to retrieve spatially resolved estimates of the column-averaged CO2 dry-air mole fraction, XCO2. Variations of XCO2 in space and time are then analyzed in the context of the atmospheric transport to quantify surface sources and sinks of CO2. This is a particularly challenging remote-sensing observation because all but the largest emission sources and natural absorbers produce only small (< 0.25 %) changes in the background XCO2 field. High measurement precision is therefore essential to resolve these small variations, and high accuracy is needed because small biases in the retrieved XCO2 distribution could be misinterpreted as evidence for CO2 fluxes. To meet its demanding measurement requirements, each OCO-2 spectrometer channel collects 24 spectra s−1 across a narrow (< 10 km) swath as the observatory flies over the sunlit hemisphere, yielding almost 1 million soundings each day. On monthly timescales, between 7 and 12 % of these soundings pass the cloud screens and other data quality filters to yield full-column estimates of XCO2. Each of these soundings has an unprecedented combination of spatial resolution (< 3 km2/sounding), spectral resolving power (λ∕Δλ > 17 000), dynamic range (∼ 104), and sensitivity (continuum signal-to-noise ratio > 400). The OCO-2 instrument performance was extensively characterized and calibrated prior to launch. In general, the instrument has performed as expected during its first 18 months in orbit. However, ongoing calibration and science analysis activities have revealed a number of subtle radiometric and spectroscopic challenges that affect the yield and quality of the OCO-2 data products. These issues include increased numbers of bad pixels, transient artifacts introduced by cosmic rays, radiance discontinuities for spatially non-uniform scenes, a misunderstanding of the instrument polarization orientation, and time-dependent changes in the throughput of the oxygen A-band channel. Here, we describe the OCO-2 instrument, its data products, and its on-orbit performance. We then summarize calibration challenges encountered during its first 18 months in orbit and the methods used to mitigate their impact on the calibrated radiance spectra distributed to the science community.
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The Measurements of Pollution in the Troposphere (MOPITT) instrument is the only satellite-borne sensor in operation that uses both thermal (TIR) and near-infrared (NIR) channels to estimate CO ...profiles. With more than 15 years (2000 to present) of validated multispectral observations, MOPITT provides the unique capability to separate CO in the lowermost troposphere (LMT, surface to 3 km (∼ 700 hPa)) from the free-tropospheric abundance. To extend this record, a new, hyper-spectral approach is presented here that will provide CO data products exceeding the capabilities of MOPITT by combining the short-wavelength infrared (SWIR, equivalent to the MOPITT NIR) channels from the TROPOspheric Monitoring Instrument (TROPOMI) to be launched aboard the European Sentinel 5 Precursor (S5p) satellite in 2016 and the TIR channels from the Cross-track Infrared Sounder (CrIS) aboard the Suomi National Polar-orbiting Partnership (Suomi NPP) satellite. We apply the MUlti-SpEctra, MUlti-SpEcies, Multi-SEnsors (MUSES) retrieval algorithm to quantify the potential of this joint CO product. CO profiles are retrieved from a single-footprint, full-spectral-resolution CrIS transect over Africa on 27–28 August 2013 coincident with significant biomass burning. Comparisons of collocated CrIS and MOPITT CO observations for the LMT show a mean difference of 2.8 ± 24.9 ppb, which is well within the estimated measurement uncertainty of both sensors. The estimated degrees of freedom (DOF) for CO signals from synergistic CrIS–TROPOMI retrievals are approximately 0.9 in the LMT and 1.3 above the LMT, which indicates that the LMT CO can be distinguished from the free troposphere, similar to MOPITT multispectral observations (0.8 in the LMT, and 1.1 above the LMT). In addition to increased sensitivity, the combined retrievals reduce measurement uncertainty, with ∼ 15 % error reduction in the LMT. With a daily global coverage and a combined spatial footprint of 14 km, the joint CrIS–TROPOMI measurements have the potential to extend and improve upon the MOPITT multispectral CO data records for the coming decade.
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With three imaging grating spectrometers, the Orbiting Carbon Observatory-2 (OCO-2)measures high spectral resolution spectra (λ/∆λ≈19,000) of reflected solar radiation within the molecular oxygen ...(O2) A-band at 0.765 μm and two carbon dioxide (CO2) bands at 1.61 and 2.06 μm. OCO-2 uses onboard lamps with a reflective diffuser, solar observations through a transmissive diffuser, lunar measurements, and surface targets for radiometric calibration and validation. Separating calibrator aging from instrument degradation poses a challenge to OCO-2. Here we present a methodology for trending the OCO-2 Build 8R radiometric calibration using OCO-2 nadir observations over eight desert sites and nearly simultaneous observations from Moderate Resolution Imaging Spectroradiometer (MODIS) with sensor viewing zenith angles of 15 ± 0.5°. For the O2 A-band, this methodology is able to quantify a drift of−0.8 ± 0.1% per year and capture a small error in correcting the aging of the solar calibrator. For the other two OCO-2 bands, no measurable changes were seen, indicating less than 0.1% and less than 0.3% per year drift in the radiometric calibration of Band 2 and Band 3, respectively.
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The first study of the global distribution of atmospheric phosgene (COCl2) has been performed using solar occultation measurements from the Atmospheric Chemistry Experiment (ACE) satellite mission. A ...total of 5614 measured profiles spanning the period February 2004 through May 2006 were used in the study. The phosgene concentrations display a zonally symmetric pattern with the maximum concentration located approximately over the equator at about 25 km in altitude and the concentration decreases towards the poles. A layer of enhanced concentration of phosgene spans the lower stratosphere over all latitudes, with volume mixing ratios of 20–60 pptv. The ACE observations show lower phosgene concentrations in the stratosphere than were obtained from previous observations in the 1980s and 1990s. This has been attributed to a significant decrease in its source species, particularly two major sources CH3CCl3 and CCl4, since the introduction of restrictions required by the Montreal Protocol and its amendments.
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FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
This overview paper highlights the successes of the Ozone Monitoring Instrument (OMI) on board the Aura satellite spanning a period of nearly 14 years. Data from OMI has been used in a wide range of ...applications and research resulting in many new findings. Due to its unprecedented spatial resolution, in combination with daily global coverage, OMI plays a unique role in measuring trace gases important for the ozone layer, air quality, and climate change. With the operational very fast delivery (VFD; direct readout) and near real-time (NRT) availability of the data, OMI also plays an important role in the development of operational services in the atmospheric chemistry domain.
The short-wave infrared (SWIR) module of the Tropospheric Monitoring Instrument (TROPOMI) on board the ESA's Sentinel-5 precursor (S5p) satellite has been very stable during its 5 years in orbit. ...Calibration was performed on the ground, complemented by measurements during in-flight instrument commissioning. The radiometric response and general performance of the SWIR module are monitored by on-board calibration sources. We show that after 5 years in orbit, TROPOMI-SWIR has continued to show excellent performance with degradation of at most 0.1 % in transmission and having lost less than 0.3 % of the detector pixels. Independent validation of the instrument calibration, via vicarious calibration, can be done through comparisons with ground-based reflectance data. In this work, ground measurements at the Railroad Valley Playa, a valley in central Nevada that is often used as a reference for satellite measurements, are used to perform vicarious calibration of the TROPOMI-SWIR measurements. This is done using dedicated measurement campaigns as well as automated reflectance measurements within the RADCALNET programme. As such, TROPOMI-SWIR is an excellent test case to explore the methodology of vicarious calibration applied to infrared spectroscopy. Using methodology developed for the vicarious calibration of the OCO-2 and GOSAT missions, the absolute radiometry of TROPOMI-SWIR performance is independently verified to be stable down to â¼ 6 %-10 % using the Railroad Valley when both the absolute and relative radiometric calibrations are applied. Differences with the on-board calibration originate from the bidirectional reflection distribution function (BRDF) effects of the desert surface, the large variety in viewing angles, and the different sizes of footprints of the TROPOMI pixels. Vicarious calibration is shown to be an additional valuable tool in validating radiance-level performances of infrared instruments such as TROPOMI-SWIR in the field of atmospheric composition. It remains clear that for instruments of similar design and resolution to TROPOMI-SWIR, on-board calibration sources will continue to provide superior results due to the limitations of the vicarious calibration method.
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We present an analysis of uncertainties in global measurements of the column averaged dry-air mole fraction of CO2 (XCO2) by the NASA Orbiting Carbon Observatory-2 (OCO-2). The analysis is based on ...our best estimates for uncertainties in the OCO-2 operational algorithm and its inputs, and uses simulated spectra calculated for the actual flight and sounding geometry, with measured atmospheric analyses. The simulations are calculated for land nadir and ocean glint observations. We include errors in measurement, smoothing, interference, and forward model parameters. All types of error are combined to estimate the uncertainty in XCO2 from single soundings, before any attempt at bias correction has been made. From these results we also estimate the "variable error" which differs between soundings, to infer the error in the difference of XCO2 between any two soundings. The most important error sources are aerosol interference, spectroscopy, and instrument calibration. Aerosol is the largest source of variable error. Spectroscopy and calibration, although they are themselves fixed error sources, also produce important variable errors in XCO2. Net variable errors are usually <1ppm over ocean and ∼ 0.5-2.0 ppm over land. The total error due to all sources is ∼ 1.5-3.5ppm over land and ∼ 1.5-2.5ppm over ocean.
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The Orbiting Carbon Observatory-2 (OCO-2) is the first National Aeronautics and Space Administration (NASA) satellite designed to measure atmospheric carbon dioxide (CO2) with the accuracy, ...resolution, and coverage needed to quantify CO2 fluxes (sources and sinks) on regional scales. OCO-2 was successfully launched on 2 July 2014 and has gathered more than 2 years of observations. The v7/v7r operational data products from September 2014 to January 2016 are discussed here. On monthly timescales, 7 to 12 % of these measurements are sufficiently cloud and aerosol free to yield estimates of the column-averaged atmospheric CO2 dry air mole fraction, XCO2, that pass all quality tests. During the first year of operations, the observing strategy, instrument calibration, and retrieval algorithm were optimized to improve both the data yield and the accuracy of the products. With these changes, global maps of XCO2 derived from the OCO-2 data are revealing some of the most robust features of the atmospheric carbon cycle. This includes XCO2 enhancements co-located with intense fossil fuel emissions in eastern US and eastern China, which are most obvious between October and December, when the north–south XCO2 gradient is small. Enhanced XCO2 coincident with biomass burning in the Amazon, central Africa, and Indonesia is also evident in this season. In May and June, when the north–south XCO2 gradient is largest, these sources are less apparent in global maps. During this part of the year, OCO-2 maps show a more than 10 ppm reduction in XCO2 across the Northern Hemisphere, as photosynthesis by the land biosphere rapidly absorbs CO2. As the carbon cycle science community continues to analyze these OCO-2 data, information on regional-scale sources (emitters) and sinks (absorbers) which impart XCO2 changes on the order of 1 ppm, as well as far more subtle features, will emerge from this high-resolution global dataset.
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