A high-resolution simulation of CO2 at 1×1 km horizontal resolution using the Weather Research and Forecasting Greenhouse gas (WRF-GHG) model was conducted, focusing on the Kanto region in Japan. The WRF-GHG simulations were performed using different anthropogenic emission inventories: EAGrid (Japan, 1 km), EDGAR (0.1o), and EDGAR-downscaled (0.01o). Our analysis showed that the simulations using EAGrid better captured the diurnal variability in observed CO2 compared to EDGAR and EDGAR-downscaled emissions at two continuous monitoring sites. The 1×1 km simulation performed better in simulating CO2 variability observed in surface sites (hourly) and aircraft observations, compared to the 27×27 km simulations. We compared the vertical profile distribution of CO2 and found that all the simulations performed similarly. During February (May), the anthropogenic (land biosphere) fluxes were the primary contributor to the vertical distribution of CO2 up to an altitude of 3200 m (4500 m), beyond which long-range transport influenced by lateral boundary conditions from Eurasia played a greater role. The sensitivity analysis of boundary conditions showed a systematic bias (~ 4 ppm) persisting above 3200 m altitude when fixed (a constant value) boundary conditions are applied, as compared to the simulation with boundary conditions from a global model. We also compared the WRF-GHG simulated column-averaged XCO2 from Orbiting Carbon Observatory-2 (OCO-2) satellite and found a statistically significant spatial correlation (r=0.47) in February. However, we found a weaker spatial correlation (0.17) in May, which could be caused due to under-representation of intense land biosphere activity in WRF-GHG.

The long-term net sink of carbon (C), nitrogen (N) and greenhouse gases (GHGs) in the northern permafrost region is projected to weaken or shift under climate change. But large uncertainties remain, even on present-day GHG budgets. We compare bottom-up (data-driven upscaling, process-based models) and top-down budgets (atmospheric inversion models) of the main GHGs (CO2, CH4, and N2O) and lateral fluxes of C and N across the region over 2000-2020. Bottom-up approaches estimate higher land to atmosphere fluxes for all GHGs compared to top-down atmospheric inversions. Both bottom-up and top-down approaches respectively show a net sink of CO2 in natural ecosystems (-31 (-667, 559) and -587 (-862, -312), respectively) but sources of CH4 (38 (23, 53) and 15 (11, 18) Tg CH4-C yr-1) and N2O (0.6 (0.03, 1.2) and 0.09 (-0.19, 0.37) Tg N2O-N yr-1) in natural ecosystems. Assuming equal weight to bottom-up and top-down budgets and including anthropogenic emissions, the combined GHG budget is a source of 147 (-492, 759) Tg CO2-Ceq yr-1 (GWP100). A net CO2 sink in boreal forests and wetlands is offset by CO2 emissions from inland waters and CH4 emissions from wetlands and inland waters, with a smaller additional warming from N2O emissions. Priorities for future research include representation of inland waters in process-based models and compilation of process-model ensembles for CH4 and N2O. Discrepancies between bottom-up and top-down methods call for analyses of how prior flux ensembles impact inversion budgets, more in-situ flux observations and improved resolution in upscaling.

East Asia (China, Japan, Koreas and Mongolia) has been the world’s economic engine over at least the past two decades, exhibiting a rapid increase in fossil fuel emissions of greenhouse gases (GHGs) and has expressed the recent ambition to achieve climate neutrality by mid-century. However, the GHG balance of its terrestrial ecosystems remains poorly constrained. Here, we present a synthesis of the three most important long-lived greenhouse gases (CO2, CH4 and N2O) budgets over East Asia during the decades of 2000s and 2010s, following a dual constraint bottom-up and top-down approach. We estimate that terrestrial ecosystems in East Asia is close to neutrality of GHGs, with a magnitude of between 196.9 ± 527.0 Tg CO2eq yr-1 (the top-down approach) and -20.8 ± 205.5 Tg CO2eq yr-1 (the bottom-up approach) during 2000-2019. This net GHG emission includes a large land CO2 sink (-1251.3 ± 456.9 Tg CO2 yr-1 based on the top-down approach and -1356.1 ± 155.6 Tg CO2 yr-1 based on the bottom-up approach), which is being fully offset by biogenic CH4 and N2O emissions, predominantly coming from the agricultural sector. Emerging data sources and modelling capacities have helped achieve agreement between the top-down and bottom-up approaches to within 20% for all three GHGs, but sizeable uncertainties remain in several flux terms. For example, the reported CO2 flux from land use and land cover change varies from a net source of more than 300 Tg CO2 yr-1 to a net sink of ~-700 Tg CO2 yr-1.

We present a comparison of atmospheric transport models that simulate carbonyl sulfide (COS). This is part II of the ongoing Atmospheric Transport Model (ATM) Inter-comparison Project (TransCom–COS). Differently from part I, we focus on seven model intercomparison by transporting two recent COS inversions of NOAA surface data within TM5-4DVAR and LMDz models. The main goals of TransCom-COS part II are (a) to compare the COS simulations using the two sets of optimized fluxes with simulations that use a control scenario (part I) and (b) to evaluate the simulated tropospheric COS abundance with aircraft-based observations from various sources. The output of the seven transport models are grouped in terms of their vertical mixing strength: strong and weak mixing. The results indicate that all transport models capture the meridional distribution of COS at the surface well. Model simulations generally match the aircraft campaigns HIPPO and ATom. Comparisons to HIPPO and ATom demonstrate a gap between observed and modelled COS over the Pacific Ocean at 0–40N, indicating a potential missing source in the free troposphere. The effects of seasonal continental COS uptake by the biosphere, observed on HIPPO and ATom over oceans, is well reproduced by the simulations. We found that the strength of the vertical mixing within the column as represented in the various atmospheric transport models explains much of the model to model differences. We also found that weak-mixing models transporting the optimized flux derived from the strong-mixing TM5 model show a too strong seasonal cycle at high latitudes.

In the framework of the RECCAP2 initiative, we present the greenhouse gas (GHG) and carbon (C) budget of Europe. For the decade of the 2010s, we present a bottom-up (BU) estimate of GHG net-emissions of 3.9 Pg CO2-eq. yr-1 (global warming potential on 100 year horizon), and are largely dominated by fossil fuel emissions. In this decade, terrestrial ecosystems are a net GHG sink of 0.9 Pg CO2-eq. yr-1, dominated by a CO2 sink. For CH4 and N2O, we find good agreement between BU and top-down (TD) estimates from atmospheric inversions. However, our BU land CO2 sink is significantly higher than TD estimates. We further show that decadal averages of GHG net-emissions have declined by 1.2 Pg CO2-eq. yr-1 since the 1990s, mainly due to a reduction in fossil fuel emissions. In addition, based on both data driven BU and TD estimates, we also find that the land CO2 sink has weakened over the past two decades. In particular, we identified a decreasing sink strength over Scandinavia, which can be attributed to an intensification of forest management. These are partly offset by increasing CO2 sinks in parts of Eastern Europe and Northern Spain, attributed in part to land use change. Extensive regions of high CH4 and N2O emissions are mainly attributed to agricultural activities and are found in Belgium, the Netherlands and the southern UK. We further analyzed interannual variability in the GHG budgets. The drought year of 2003 shows the highest net-emissions of CO2 and of all GHGs combined.

Nitrous oxide (N2O) is the most important stratospheric ozone-depleting agent based on current emissions and the third largest contributor to increased net radiative forcing. Increases in atmospheric N2O have been attributed primarily to enhanced soil N2O emissions. Critically, contributions from soils in the Northern High Latitudes (NHL, >50°N) remain poorly quantified despite their vulnerability to permafrost thawing induced by climate change. An ensemble of six terrestrial biosphere models suggests NHL soil N2O emissions doubled since the preindustrial 1860s, increasing on average by 2.0±1.0 Gg N yr-1 (p<0.01). This trend reversed after the 1980s because of reduced nitrogen fertilizer application in non-permafrost regions and increased plant growth due to CO2 fertilization suppressed emissions. However, permafrost soil N2O emissions continued increasing attributable to climate warming; the interaction of climate warming and increasing CO2 concentrations on nitrogen and carbon cycling will determine future trends in NHL soil N2O emissions.

Inverse modelling method named Maximum likelihood Ensemble Filter (MLEF) was used to estimate gridded surface CO fluxes using continuous, flask and Comprehensive Observation Network for TRace gases by AIrLiner (CONTRAIL) data for the years 2009-2011. Here, MLEF coupled with Parametric Chemistry Transport Model (PCTM) driven by Modern-Era Retrospective analysis for Research and Applications, Version 2 (MERRA2) weather data has been used. Flux estimation was done by solving separate multiplicative biases for photosynthesis, respiration, and air-sea gas exchange fluxes. Hourly land fluxes derived from Simple Biosphere-version 3 (SiB3) model, Takahashi ocean fluxes and Brenkert fossil fuel emissions were used as the prior fluxes. The inversion was carried out by assimilating hourly CO observations, According to this study, North America showed about 60-80% uncertainty reduction while the Asian and European regions showed moderate results with 50-60% uncertainty reduction. Most other land and oceanic regions showed less than 30% uncertainty reduction. The results were mainly compared with well-known CarbonTracker and some parallel inversion studies by considering long-term averages of the estimated fluxes for the TransCom regions. Boreal North America, Temperate North America and Australia showed similar annual averages in each case. Tropical Asia and Europe showed comparable results with all other studies except for the CarbonTracker. The biases were poorly constrained in the regions having few measurement sites like South America, Africa and Eurasian Temperate which showed completely different result with other studies.

We present a comparison of atmospheric transport model simulations for carbonyl sulfide (COS), within the framework of the ongoing atmospheric tracer transport model intercomparison project “TransCom”. Seven atmospheric transport models participated in the inter-comparison experiment and provided simulations of COS mixing ratios in the troposphere over a 9-year period (2010–2018), using prescribed state-of-the-art surface fluxes for various components of the atmospheric COS budget: biospheric sink, oceanic source, sources from fire and industry. Since the biosphere is the largest sink of COS, we tested sink estimates produced by two different biosphere models. The main goals of TransCom-COS are (a) to investigate the impact of the transport uncertainty and emission distribution in simulating the spatio-temporal variability of COS mixing ratios in the troposphere, and (b) to assess the sensitivity of simulated tropospheric COS mixing ratios to the seasonal and diurnal variability of the COS biosphere fluxes. To this end, a control case with state-of-the-art seasonal fluxes of COS was constructed. Models were run with the same fluxes and without chemistry to isolate transport differences. Further, two COS flux scenarios were compared: one using a biosphere flux with a monthly time resolution and the other using a biosphere flux with a three-hourly time resolution. In addition, we investigated the sensitivity of the simulated concentrations to different biosphere fluxes and to indirect oceanic emissions through dimethylsulfide (DMS) and carbon disulfide (CS2). The modelled COS mixing ratios were assessed against in-situ observations from surface stations and aircraft.

Understanding terrestrial ecosystems and their response to anthropogenic climate change requires quantification of land-atmosphere carbon exchange. However, top-down and bottom-up estimates of large-scale land-atmosphere fluxes, including the northern extratropical growing season net flux (GSNF), show significant discrepancies. We develop a data-driven metric for the GSNF using atmospheric carbon dioxide concentration observations collected during the High-Performance Instrumented Airborne Platform for Environmental Research (HIAPER) Pole-to-Pole Observations (HIPPO) and Atmospheric Tomography Mission (ATom) flight campaigns. This aircraft-derived metric is bias corrected using three independent atmospheric inversion systems. We estimate the northern extratropical GSNF to be 5.7 ± 0.2 Pg C and use it to evaluate net biosphere productivity from the Coupled Model Intercomparison Project phase 5 and 6 (CMIP5 and CMIP6) models. While the model-to-model spread in the GSNF has decreased in CMIP6 models relative to that of the CMIP5 models, there is still disagreement on the magnitude and timing of seasonal carbon uptake with most models underestimating the GSNF and overestimating the length of the growing season relative to the observations. We also use an emergent constraint approach to estimate annual northern extratropical gross primary productivity to be 56 ± 15 Pg C, heterotrophic respiration to be 25 ± 11 Pg C, and net primary productivity to be 28 ± 10 Pg C. The flux inferred from these aircraft observations provides an additional constraint on large-scale, gross fluxes in prognostic Earth system models that may ultimately improve our ability to accurately predict carbon-climate feedbacks.