The Japanese Global Observing SATellite for Greenhouse gases and Water cycle (GOSAT-GW) will be an Earth-observing satellite to conduct global observations of atmospheric carbon dioxide (CO2), methane (CH4), and nitrogen dioxide (NO2) simultaneously from a single platform. GOSAT-GW is the third satellite in the series of the currently operating Greenhouse gases Observing SATellite (GOSAT) and GOSAT-2. It will carry two sensors, the Total Anthropogenic and Natural emissions mapping SpectrOmeter-3 (TANSO-3) and the Advanced Microwave Scanning Radiometer 3 (AMSR3), with the latter dedicated to the observation of physical parameters related to the water cycle. TANSO-3 is a high-resolution grating spectrometer designed to measure reflected sunlight in the visible to short-wave infrared spectral ranges. It aims to retrieve the column-averaged dry-air mole fractions of CO2 and CH4 (denoted as XCO2 and XCH4, respectively), as well as the vertical column density of tropospheric NO2. The TANSO-3 sensor onboard GOSAT-GW will utilize the wavelength bands of 0.45, 0.76, and 1.61 µm for NO2, O2, and CO2 and CH4 retrievals, respectively. GOSAT-GW will fly in a sun-synchronous orbit with a local overpass time of approximately 13:30 and a 3-day ground-track repeat cycle. The TANSO-3 sensor has two observation modes in the push-broom operation: Wide Mode, which provides globally covered maps with a 10-km spatial resolution within 3 days, and Focus Mode, which provides snapshot maps over targeted areas with a high spatial resolution of 1–3 km. The objectives of the GOSAT-GW mission include (1) monitoring atmospheric global-mean concentrations of greenhouse gasses (GHGs), (2) verifying national anthropogenic GHG emissions inventories, and (3) detecting GHG emissions from large sources, such as megacities and power plants. A comprehensive validation exercise will be conducted to ensure that the sensor products’ quality meets the required precision to achieve the above objectives. With a projected operational lifetime of seven years, GOSAT-GW will provide vital space-based constraints on both anthropogenic and natural GHG emissions. These measurements will contribute significantly to climate change mitigation efforts, particularly by supporting the Global Stocktake (GST) mechanism, a key element of the Paris Agreement.
Combined NO2 and CO2 observations have the potential to constrain the identification of the locations and strength of urban CO2 emissions, in particular, point sources such as power plants. We report the first results of airborne spectroscopic NO2 and CO2 observations over an urban area in Japan in February 2018. Inversed emission rates of two stacks of the coal‐fired power plant for CO2 showed relatively good agreement with those estimated by a bottom‐up inventory—the Regional Emission inventory in ASia (REAS) v3.1—within −7% to 40% because the plume shapes were well identified due to constraint by NO2 measurements. The estimated NOx emission rates showed discrepancies more than 80% with those estimated by the REAS v3.1, mainly due to the uncertainties in activity data and emission factors, or in the greatly varying NO/NO2 ratios in fresh plumes, which warrant further investigations when estimating NOx emissions from satellite NO2 observations on km‐scales.
6 November 2016 in Rapid Communications in Mass Spectrometry
No direct observational evidence of sprite‐produced active radicals has been presented owing to the difficulty of observing a small event area in the nighttime mesosphere, whereas sprite chemical models have indicated that sprite discharge locally affects the atmospheric composition. We present the first observational evidence of a HO2 production above sprite‐producing thunderstorms from the coincidence of temporal‐spatial observations of HO2 spectra, sprite events, and thunderstorms by two space instruments, a submillimeter‐wave limb spectrometer and UV/VIS Imager, as well as a ground‐based very‐low‐frequency radiation lightning detection network. A total of three areas were identified with enhanced HO2 levels of approximately 1025 molecules. A chemical sprite model indicates an increase in HO2 in the considered altitude region; however, the predicted production due to a single sprite event is smaller than the observed enhancement. Our observational results suggest that sprites potentially contribute 1% of nighttime background HO2 generation at altitudes of 75‐‐80,km globally.
Acetonitrile (CH3CN) is a volatile organic compound (VOC) and a potential tracer of biomass burning. We evaluated the capability of using observations derived from the Superconducting Submillimeter-Wave Limb-Emission Sounder (SMILES) on the International Space Station (ISS) to measure CH3CN profiles. The error in a CH3CN vertical profile from the Level-2 research (L2r) product version 3.0.0 was estimated by theoretical error analysis and also compared with other instrumental measurements. We estimated the systematic and random errors to be ∼5.8 ppt (7.8 %) and 25 ppt (60 %), respectively, for a single observation at 15.7 hPa in the tropics, where the CH3CN measurements are enhanced. The major source of systematic error was the pressure-broadening coefficient, and its contribution to the total systematic error was approximately 60 % in the middle stratosphere (15.7–4.8 hPa). The random error decreased to less than 40 % after averaging 10 profiles in the pressure range of 28.8–1.6 hPa. The total error due to uncertainties in other molecular spectroscopic parameters (2.8 ppt) was comparable to that of CH3CN spectroscopic parameters. We compared the SMILES CH3CN profiles with those of the microwave limb sounder (MLS) on the Aura satellite (version 4.2). The SMILES CH3CN values were consistent with those from MLS within the standard deviation (1σ) of the MLS observations. The difference between the SMILES and MLS CH3CN profiles increased with altitude and was within 20–35 ppt (20 %–260 %) at 15.7–1.6 hPa. We observed discrepancies of 5–10 ppt (10 %–30 %) between the SMILES CH3CN profiles observed by different spectrometers, and hence, we do not recommend merging SMILES CH3CN profiles derived from different spectrometers. We found that the SMILES CH3CN volume mixing ratio (VMR) in the upper stratosphere has a seasonal maximum in February.