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We apply atmospheric methane column retrievals from two different satellite instruments (Greenhouse gases Observing SATellite – GOSAT; TROPOspheric Monitoring Instrument – TROPOMI) to a regional inversion framework to quantify East Asian methane emissions for 2019 at 0.5 ∘ × 0.625 ∘ horizontal resolution. The goal is to assess if GOSAT (relatively mature but sparse) and TROPOMI (new and dense) observations inform consistent methane emissions from East Asia with identically configured inversions. Comparison of the results from the two inversions shows similar correction patterns to the prior inventory in central northern China, central southern China, northeastern China, and Bangladesh, with less than 2.6 Tg a -1 differences in regional posterior emissions. The two inversions, however, disagree over some important regions, particularly in northern India and eastern China. The methane emissions inferred from GOSAT observations are 7.7 Tg a -1 higher than those from TROPOMI observations over northern India but 6.4 Tg a -1 lower over eastern China. The discrepancies between the two inversions are robust against varied inversion configurations (i.e., assimilation window and error specifications). We find that the lower methane emissions from eastern China inferred by the GOSAT inversion are more consistent with independent ground-based in situ and total column (TCCON) observations, indicating that the TROPOMI retrievals may have high XCH 4 biases in this region. We also evaluate inversion results against tropospheric aircraft observations over India during 2012–2014 by using a consistent GOSAT inversion of earlier years as an intercomparison platform. This indirect evaluation favors lower methane emissions from northern India inferred by the TROPOMI inversion. We find that in this case the discrepancy in emission inference is contributed by differences in data coverage (almost no observations by GOSAT vs. good spatial coverage by TROPOMI) over the Indo-Gangetic Plain. The two inversions also differ substantially in their posterior estimates for northwestern China and neighboring Kazakhstan, which is mainly due to seasonally varying biases between GOSAT and TROPOMI XCH 4 data that correlate with changes in surface albedo. [ABSTRACT FROM AUTHOR]

Atmospheric CO2 mole fractions are observed at Beijing (BJ), Xianghe (XH), and Xinglong (XL) in North China using Picarro G2301 cavity ring-down spectroscopy instruments. The measurement system is described comprehensively for the first time. The geographical distances among these three sites are within 200 km , but they have very different surrounding environments: BJ is inside the megacity; XH is in the suburban area; XL is in the countryside on a mountain. The mean and standard deviation of CO2 mole fractions at BJ, XH, and XL between October 2018 and September 2019 are 448.4±12.8 , 436.0±9.2 , and 420.6±8.2 ppm , respectively. The seasonal variations of CO2 at these three sites are similar, with a maximum in winter and a minimum in summer, which is dominated by the terrestrial ecosystem. However, the seasonal variations of CO2 at BJ and XH are more affected by human activities as compared to XL. Using CO2 at XL as the background, CO2 enhancements are observed simultaneously at BJ and XH. The diurnal variations of CO2 are driven by the boundary layer height, photosynthesis, and human activities at BJ, XH, and XL. We also compare the CO2 measurements at BJ, XH, and XL with five urban sites in the USA, and it is found that the CO2 mean concentration at BJ is the largest. Moreover, we address the impact of the wind on the CO2 mole fractions at BJ and XL. This study provides an insight into the spatial and temporal variations of CO2 mole fractions in North China. [ABSTRACT FROM AUTHOR]

The seasonal evolution of O3 and its photochemical production regime in a polluted region of eastern China between 2014 and 2017 has been investigated using observations. We used tropospheric ozone (O3), carbon monoxide (CO), and formaldehyde (HCHO, a marker of VOCs (volatile organic compounds)) partial columns derived from high-resolution Fourier transform spectrometry (FTS); tropospheric nitrogen dioxide (NO2, a marker of NOx (nitrogen oxides)) partial column deduced from the Ozone Monitoring Instrument (OMI); surface meteorological data; and a back trajectory cluster analysis technique. A broad O3 maximum during both spring and summer (MAM/JJA) is observed; the day-to-day variations in MAM/JJA are generally larger than those in autumn and winter (SON/DJF). Tropospheric O3 columns in June are 1.55 x 1018 molecules cm-2 (56DU (Dobson units)), and in December they are 1.05 x 1018 molecules cm-2 (39 DU). Tropospheric O3 columns in June were *** 50% higher than those in December. Compared with the SON/DJF season, the observed tropospheric O3 levels in MAM/JJA are more influenced by the transport of air masses from densely populated and industrialized areas, and the high O3 level and variability in MAM/JJA is determined by the photochemical O3 production. The tropospheric-column HCHO/NO2 ratio is used as a proxy to investigate the photochemical O3 production rate (PO3). The results show that the PO3 is mainly nitrogen oxide (NOx) limited in MAM/JJA, while it is mainly VOC or mixed VOC--NOx limited in SON/DJF. Statistics show that NOx-limited, mixed VOC--NOx-limited, and VOC-limited PO3 accounts for 60.1 %, 28.7 %, and 11% of days, respectively. Considering most of PO3 is NOx limited or mixed VOC--NOx limited, reductions in NOx would reduce O3 pollution in eastern China. [ABSTRACT FROM AUTHOR]

Atmospheric carbon monoxide (CO) and methane (CH4) mole fractions are measured by ground-based in situ cavity ring-down spectroscopy (CRDS) analyzers and Fourier transform infrared (FTIR) spectrometers at two sites (St Denis and Maïdo) on Reunion Island (21° S, 55° E) in the Indian Ocean. Currently, the FTIR Bruker IFS 125HR at St Denis records the direct solar spectra in the near-infrared range, contributing to the Total Carbon Column Observing Network (TCCON). The FTIR Bruker IFS 125HR at Maïdo records the direct solar spectra in the mid-infrared (MIR) range, contributing to the Network for the Detection of Atmospheric Composition Change (NDACC). In order to understand the atmospheric CO and CH4 variability on Reunion Island, the time series and seasonal cycles of CO and CH4 from in situ and FTIR (NDACC and TCCON) measurements are analyzed. Meanwhile, the difference between the in situ and FTIR measurements are discussed. The CO seasonal cycles observed from the in situ measurements at Maïdo and FTIR retrievals at both St Denis and Maïdo are in good agreement with a peak in September-November, primarily driven by the emissions from biomass burning in Africa and South America. The dry-air column averaged mole fraction of CO (XCO) derived from the FTIR MIR spectra (NDACC) is about 15.7 ppb larger than the CO mole fraction near the surface at Maïdo, because the air in the lower troposphere mainly comes from the Indian Ocean while the air in the middle and upper troposphere mainly comes from Africa and South America. The trend for CO on Reunion Island is unclear during the 2011-2017 period, and more data need to be collected to get a robust result. A very good agreement is observed in the tropospheric and stratospheric CH4 seasonal cycles between FTIR (NDACC and TCCON) measurements, and in situ and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) satellite measurements, respectively. In the troposphere, the CH4 mole fraction is high in August-September and low in December-January, which is due to the OH seasonal variation. In the stratosphere, the CH4 mole fraction has its maximum in March-April and its minimum in August-October, which is dominated by vertical transport. In addition, the different CH4 mole fractions between the in situ, NDACC and TCCON CH4 measurements in the troposphere are discussed, and all measurements are in good agreement with the GEOS-Chem model simulation. The trend of XCH4 is 7.6±0.4 ppb yr-1 from the TCCON measurements over the 2011 to 2017 time period, which is consistent with the CH4 trend of 7.4±0.5 ppb yr-1 from the in situ measurements for the same time period at St Denis. [ABSTRACT FROM AUTHOR]