We have used an AGCM (atmospheric general circulation model)-based Chemistry Transport Model (ACTM) for the simulation of methane (CH 4 ) in the height range of earth's surface to about 90 km. The model simulations are compared with measurements at hourly, daily, monthly and interannual time scales by filtering or averaging all the timeseries appropriately. From this model-observation comparison, we conclude that the recent (1990)(1991)(1992)(1993)(1994)(1995)(1996)(1997)(1998)(1999)(2000)(2001)(2002)(2003)(2004)(2005)(2006) trends in growth rate and seasonal cycle at most measurement sites can be fairly successfully modeled by using existing knowledge of CH 4 flux trends and seasonality. A large part of the interannual variability (IAV) in CH 4 growth rate is apparently controlled by IAV in atmospheric dynamics at the tropical sites and forest fires in the high latitude sites. The flux amplitudes are optimized with respect to the available hydroxyl radical (OH) distribution and model transport for successful reproduction of latitudinal and longitudinal distribution of observed CH 4 mixing ratio at the earth's surface. Estimated atmospheric CH 4 lifetime in this setup is 8.6 years. We found a small impact (less than 0.5 ppb integrated over 1 year) of OH diurnal variation, due to temperature dependence of reaction rate coe‰cient, on CH 4 simulation compared to the transport related variability (order of G15 ppb at interannual timescales). Model-observation comparisons of seasonal cycles, synoptic variations and diurnal cycles are shown to be useful for validating regional flux distribution patterns and strengths. Our results, based on two emission scenarios, suggest reduced emissions from temperate and tropical Asia region (by 13, 5, 3 Tg-CH 4 for India, China and Indonesia, respectively), and compensating increase (by 9, 9, 3 Tg-CH 4 for Russia, United States and Canada, respectively) in the boreal Northern Hemisphere (NH) are required for improved model-observation agreement.

Abstract. In this study we present the retrieval of the column-averaged dry air mole fraction of carbon dioxide (X CO 2 ) from the Orbiting Carbon Observatory-2 (OCO-2) satellite observations using the RemoTeC algorithm, previously successfully applied to retrieval of greenhouse gas concentration from the Greenhouse Gases Observing Satellite (GOSAT). The X CO 2 product has been validated with collocated ground-based measurements from the Total Carbon Column Observing Network (TCCON) for almost 2 years of OCO-2 data from September 2014 to July 2016. We found that fitting an additive radiometric offset in all three spectral bands of OCO-2 significantly improved the retrieval. Based on a small correlation of the X CO 2 error over land with goodness of fit, we applied an a posteriori bias correction to our OCO-2 retrievals. In overpass averaged results, X CO 2 retrievals have an SD of ∼ 1.30 ppm and a station-tostation variability of ∼ 0.40 ppm among collocated TCCON sites. The seasonal relative accuracy (SRA) has a value of 0.52 ppm. The validation shows relatively larger difference with TCCON over high-latitude areas and some specific regions like Japan.

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Abstract. Since the late 1990s, the meteorological observatory established in Anmyeondo (36.5382° N, 126.3311° E, and 30 m above mean sea level) has been monitoring several greenhouse gases such as CO2, CH4, N2O, CFCs, and SF6 as a part of the Global Atmosphere Watch (GAW) Program. A high resolution ground-based (g-b) Fourier transform spectrometer (FTS) was installed at this observation site in 2013 and has been operated within the frame work of the Total Carbon Column Observing Network (TCCON) since August 2014. The solar spectra recorded by the g-b FTS cover the spectral range 3800 to 16 000 cm−1 at a resolution of 0.02 cm−1. In this work, the GGG2014 version of the TCCON standard retrieval algorithm was used to retrieve total column average CO2 and CH4 dry mole fractions (XCO2, XCH4) and from the FTS spectra. Spectral bands of CO2 (at 6220.0 and 6339.5 cm−1 center wavenumbers, CH4 at 6002 cm−1 wavenumber, and O2 near 7880 cm−1 ) were used to derive the XCO2 and XCH4. In this paper, we provide comparisons of XCO2 and XCH4 between the aircraft observations and g-b FTS over Anmyeondo station. A comparison of 13 coincident observations of XCO2 between g-b FTS and OCO-2 (Orbiting Carbon Observatory) satellite measurements are also presented for the measurement period between February 2014 and November 2017. OCO-2 observations are highly correlated with the g-b FTS measurements (r2 = 0.884) and exhibited a small positive bias (0.189 ppm). Both data set capture seasonal variations of the target species with maximum and minimum values in spring and late summer, respectively. In the future, it is planned to further utilize the FTS measurements for the evaluation of satellite observations such as Greenhouse Gases Observing Satellite (GOSAT, GOSAT-2). This is the first report of the g-b FTS observations of XCO2 species over the Anmyeondo station.

In this study we present the retrieval of the column averaged dry air mole fraction of carbon dioxide (XCO2) from the Orbiting Carbon Observatory-2 (OCO-2) satellite observations using the RemoTeC algorithm, previously successfully applied to retrieval of greenhouse gas concentration from the Greenhouse Gases Observing Satellite (GOSAT). The XCO2 product has been validated with collocated ground based measurements from the Total Carbon Column Observing Network (TCCON) for almost 2 years of OCO-2 data from September 2014 to July 2016. We found that fitting an additive radiometric offset in all three spectral bands of OCO-2 significantly improved the retrieval. Based on a small correlation of the XCO2 error over land with fit residuals, we applied an a posteriori bias correction to our OCO-2 retrievals. In daily averaged results, XCO2 retrievals have a standard deviation ~ 1.30 ppm and a station-to-station variability of ~ 0.40 ppm among collocated TCCON sites. The seasonal relative accuracy (SRA) has a value of 0.52 ppm. The validation shows relatively larger difference with TCCON over high latitude areas and some specific regions like Japan

There are still large uncertainties in the estimates of net ecosystem exchange of CO2 (NEE) with atmosphere in Asia, particularly in the boreal and eastern part of temperate Asia. To understand these uncertainties, we assessed the CarbonTracker Asia (CTA2017) estimates of the spatial and temporal distributions of NEE through a comparison with FLUXCOM and the global inversion models from the Copernicus Atmospheric Monitoring Service (CAMS), Monitoring Atmospheric Composition and Climate (MACC), and Jena CarboScope in Asia, as well as examining the impact of the nesting approach on the optimized NEE flux during the 2001–2013 period. The long-term mean carbon uptake is reduced in Asia, which is −0.32 ± 0.22 PgC yr−1, whereas −0.58 ± 0.26 PgC yr−1 is shown from CT2017 (CarbonTracker global). The domain aggregated mean carbon uptake from CTA2017 is found to be lower by 23.8%, 44.8%, and 60.5% than CAMS, MACC, and Jena CarboScope, respectively. For example, both CTA2017 and CT2017 models captured the interannual variability (IAV) of the NEE flux with a different magnitude and this leads to divergent annual aggregated results. Differences in the estimated interannual variability of NEE in response to El Niño–Southern Oscillation (ENSO) may result from differences in the transport model resolutions. These inverse models’ results have a substantial difference compared to FLUXCOM, which was found to be −5.54 PgC yr−1. On the one hand, we showed that the large NEE discrepancies between both inversion models and FLUXCOM stem mostly from the tropical forests. On the other hand, CTA2017 exhibits a slightly better correlation with FLUXCOM over grass/shrub, fields/woods/savanna, and mixed forest than CT2017. The land cover inconsistency between CTA2017 and FLUXCOM is therefore one driver of the discrepancy in the NEE estimates. The diurnal averaged NEE flux between CTA2017 and FLUXCOM exhibits better agreement during the carbon uptake period than the carbon release period. Both CTA2017 and CT2017 revealed that the overall spatial patterns of the carbon sink and source are similar, but the magnitude varied with seasons and ecosystem types, which is mainly attributed to differences in the transport model resolutions. Our findings indicate that substantial inconsistencies in the inversions and FLUXCOM mainly emerge during the carbon uptake period and over tropical forests. The main problems are underrepresentation of FLUXCOM NEE estimates by limited eddy covariance flux measurements, the role of CO2 emissions from land use change not accounted for by FLUXCOM, sparseness of surface observations of CO2 concentrations used by the assimilation systems, and land cover inconsistency. This suggested that further scrutiny on the FLUXCOM and inverse estimates is most likely required. Such efforts will reduce inconsistencies across various NEE estimates over Asia, thus mitigating ecosystem-driven errors that propagate the global carbon budget. Moreover, this work also recommends further investigation on how the changes/updates made in CarbonTracker affect the interannual variability of the aggregate and spatial pattern of NEE flux in response to the ENSO effect over the region of interest.

A cavity ring-down spectroscopy (CRDS) G-2401m analyzer onboard a Beechcraft King Air 350, a new Korean Meteorological Administration (KMA) research aircraft measurement platform since 2018, has been used to measure in situ CO2, CH4, and CO. We analyzed the aircraft measurements obtained in two campaigns: a within-boundary layer survey over the western Republic of Korea (hereafter Korea) for analyzing the CO2 and CH4 emission characteristics for each season (the climate change monitoring (CM) CM mission), and a low altitude survey over the Yellow Sea for monitoring the pollutant plumes transported into Korea from China (the environment monitoring (EM) mission). This study analyzed CO2, CH4, and CO data from a total of 14 flights during 2019 season. To characterize the regional combustion sources signatures of CO2 and CH4, we calculated the short-term (1-min slope based on one second data) regression slope of CO to CO2 and CH4 to CO enhancements (subtracted with background level, present as ∆CO, ∆CO2, and ∆CH4); slope filtered with correlation coefficients (R2) (<0.4 were ignored). These short-term slope analyses seem to be sensitive to aircraft measurements in which the instrument samples short-time varying mixtures of different air masses. The EM missions all of which were affected by pollutants emitted in China, show the regression slope between ∆CO and ∆CO2 with of 1.8–6% and 0.3–0.7 between ∆CH4 and ∆CO. In particular, the regression slope between ∆CO and ∆CO2 increased to >4% when air flows from east-central China such as Hebei, Shandong, and Jiangsu provinces, etc., sustained for 1–3 days, suggesting pollutants from these regions were most likely characterized by incomplete fossil fuel combustions at the industries. Over 80% of the observations in the Western Korea missions were attributed to Korean emission sources with regression slope between ∆CO and ∆CO2 of 0.5–1.9%. The CO2 emissions hotspots were mainly located in the north-Western Korea of high population density and industrial activities. The higher CH4 were observed during summer season with the increasing concentration of approximately 6% over the background level, it seems to be attributed to biogenic sources such as rice paddies, landfill, livestock, and so on. It is also noted that occurrences of high pollution episodes in North-Western Korea are more closely related to the emissions in China than in Korea.