The Geostationary Environment Monitoring Spectrometer (GEMS) is scheduled for launch in February 2020 to monitor air quality (AQ) at an unprecedented spatial and temporal resolution from a geostationary Earth orbit (GEO) for the first time. With the development of UV–visible spectrometers at sub-nm spectral resolution and sophisticated retrieval algorithms, estimates of the column amounts of atmospheric pollutants (O3, NO2, SO2, HCHO, CHOCHO, and aerosols) can be obtained. To date, all the UV–visible satellite missions monitoring air quality have been in low Earth orbit (LEO), allowing one to two observations per day. With UV–visible instruments on GEO platforms, the diurnal variations of these pollutants can now be determined. Details of the GEMS mission are presented, including instrumentation, scientific algorithms, predicted performance, and applications for air quality forecasts through data assimilation. GEMS will be on board the Geostationary Korea Multi-Purpose Satellite 2 (GEO-KOMPSAT-2) satellite series, which also hosts the Advanced Meteorological Imager (AMI) and Geostationary Ocean Color Imager 2 (GOCI-2). These three instruments will provide synergistic science products to better understand air quality, meteorology, the long-range transport of air pollutants, emission source distributions, and chemical processes. Faster sampling rates at higher spatial resolution will increase the probability of finding cloud-free pixels, leading to more observations of aerosols and trace gases than is possible from LEO. GEMS will be joined by NASA’s Tropospheric Emissions: Monitoring of Pollution (TEMPO) and ESA’s Sentinel-4 to form a GEO AQ satellite constellation in early 2020s, coordinated by the Committee on Earth Observation Satellites (CEOS).

Abstract. Methyl bromide (CH3Br) is a potent ozone-depleting substance (ODS) that has both natural and anthropogenic sources. CH3Br has been used mainly for preplant soil fumigation, post-harvest grain and timber fumigation, and structural fumigation. Most non-quarantine and pre-shipment (non-QPS) uses were phased out by 2005 for non-Article 5 (developed) countries and by 2015 for Article 5 (developing) countries under the Montreal Protocol on Substances that Deplete the Ozone Layer; some uses have continued under critical-use exemptions (CUEs). Under the protocol, individual nations are required to report annual data on CH3Br production and consumption for quarantine–pre-shipment (QPS) uses, non-QPS uses, and CUEs to the United Nations Environment Programme (UNEP). In this study, we analyzed high-precision, in situ measurements of atmospheric mole fractions of CH3Br obtained at the Gosan station on Jeju Island, South Korea, from 2008 to 2019. The background mole fractions of CH3Br in the atmosphere at Gosan declined from 8.5±0.8 ppt (parts per trillion) in 2008 to 7.4±0.6 ppt in 2019 at a rate of -0.13±0.02 ppt yr−1. At Gosan, we also observed periods of persistent mole fractions (pollution events) elevated above the decreasing background in continental air masses from China. Statistical back-trajectory analyses showed that these pollution events are predominantly traced back to CH3Br emissions from eastern China. Using an interspecies correlation (ISC) method with the reference trace species CFC-11 (CCl3F), we estimate anthropogenic CH3Br emissions from eastern China at an average of 4.1±1.3 Gg yr−1 in 2008–2019, approximately 2.9±1.3 Gg yr−1 higher than the bottom-up emission estimates reported to UNEP. Possible non-fumigation CH3Br sources – rapeseed production and biomass burning – were assessed, and it was found that the discrepancy is most likely due to unreported or incorrectly reported QPS and non-QPS fumigation uses. These unreported anthropogenic emissions of CH3Br are confined to eastern China and account for 30 %–40 % of anthropogenic global CH3Br emissions. They are likely due to delays in the introduction of CH3Br alternatives, such as sulfuryl fluoride (SO2F2), heat, and irradiation, and a possible lack of industry awareness of the need for regulation of CH3Br production and use.

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Aerosols in the atmosphere play an essential role in the radiative transfer process due to their scattering, absorption, and emission. Moreover, they interrupt the retrieval of atmospheric properties from ground-based and satellite remote sensing. Thus, accurate aerosol information needs to be obtained. Herein, we developed an optimal-estimation-based aerosol optical depth (AOD) retrieval algorithm using the hyperspectral infrared downwelling emitted radiance of the Atmospheric Emitted Radiance Interferometer (AERI). The proposed algorithm is based on the phenomena that the thermal infrared radiance measured by a ground-based remote sensor is sensitive to the thermodynamic profile and degree of the turbid aerosol in the atmosphere. To assess the performance of algorithm, AERI observations, measured throughout the day on 21 October 2010 at Anmyeon, South Korea, were used. The derived thermodynamic profiles and AODs were compared with those of the European center for a reanalysis of medium-range weather forecasts version 5 and global atmosphere watch precision-filter radiometer (GAW-PFR), respectively. The radiances simulated with aerosol information were more suitable for the AERI-observed radiance than those without aerosol (i.e., clear sky). The temporal variation trend of the retrieved AOD matched that of GAW-PFR well, although small discrepancies were present at high aerosol concentrations. This provides a potential possibility for the retrieval of nighttime AOD.

Asian dust aerosols consist of various minerals, such as quartz, clay minerals, feldspars, and calcite. Complex refractive index of Asian dust is determined for a spectral range from 0.2 to 1.0 μm, assuming that the particles are an internal mixture of the component minerals in dust samples reported in previous literature. The derived optical constants for Asian dust are quite different from the refractive indices for other desert dusts. The imaginary refractive index for Asian dust is much smaller than that of the “mineral” model in Optical Properties of Aerosols and Clouds (OPAC) across the whole range. At wavelengths shorter than 650 nm, the present imaginary index is smaller than the index for Saharan dust, determined from mineralogical compositions of dust samples at Tinfou, Morocco, during the Saharan Mineral Dust Experiment (SAMUM). The simulated spectrum for an Asian dust event on 15 March 2009 in north‐east China using the present optical constants agree well with the spectrum measured by the Ozone Monitoring Instrument (OMI) on board the Aura spacecraft.