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 a greenhouse gas and an ozone-depleting agent with large and growing anthropogenic emissions. Previous studies identified the influx of N2O-depleted air from the stratosphere to partly cause the seasonality in tropospheric N2O (aN2O), but other contributions remain unclear. Here we combine surface fluxes from eight land and four ocean models from phase 2 of the Nitrogen/N2O Model Intercomparison Project with tropospheric transport modeling to simulate aN2O at the air sampling sites: Alert, Barrow, Ragged Point, Samoa, Ascension Island, and Cape Grim for the modern and preindustrial periods. Models show general agreement on the seasonal phasing of zonal-average N2O fluxes for most sites, but, seasonal peak-to-peak amplitudes differ severalfold across models. After transport, the seasonal amplitude of surface aN2O ranges from 0.25 to 0.80 ppb (interquartile ranges 21-52% of median) for land, 0.14 to 0.25 ppb (19-42%) for ocean, and 0.13 to 0.76 ppb (26-52%) for combined flux contributions. The observed range is 0.53 to 1.08 ppb. The stratospheric contributions to aN2O, inferred by the difference between surface-troposphere model and observations, show 36-126% larger amplitudes and minima delayed by ~1 month compared to Northern Hemisphere site observations. Our results demonstrate an increasing importance of land fluxes for aN2O seasonality, with land fluxes and their seasonal amplitude increasing since the preindustrial era and are projected to grow under anthropogenic activities. In situ aN2O observations and atmospheric transport-chemistry models will provide opportunities for constraining terrestrial and oceanic biosphere models, critical for projecting surface N2O sources under ongoing global warming.

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.

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.

In 2020, global atmospheric methane (CH4) levels increased by 14.7 parts-per-billion (ppb) - the largest annual increase since atmospheric records began in 1983 (https://research.noaa.gov/article/ArtMID/587/ArticleID/2742/Despite-pandemic-shutdowns-carbon-dioxide-and-methane-surged-in-2020) continuing an upward trend since 2007. This is concerning since CH4 is the second most important long-lived greenhouse after CO2 and has global warming potential 28 times that of CO2 per unit mass on a 100-year time scale (Myhre et al. 2013). Moreover, pathways to limit global warming to 1.5°C, or even 2.0°C, require non-CO2 emissions and, in particular, CH4 emissions, to be reduced by 35% with respect to 2010 levels by 2050 (Forster et al. 2018).