Abstract. Accurate accounting of emissions and removals of CO2 is critical for the planning and verification of emission reduction targets in support of the Paris Agreement. Here, we present a pilot dataset of country-specific net carbon exchange (NCE; fossil plus terrestrial ecosystem fluxes) and terrestrial carbon stock changes aimed at informing countries' carbon budgets. These estimates are based on “top-down” NCE outputs from the v10 Orbiting Carbon Observatory (OCO-2) modeling intercomparison project (MIP), wherein an ensemble of inverse modeling groups conducted standardized experiments assimilating OCO-2 column-averaged dry-air mole fraction (XCO2) retrievals (ACOS v10), in situ CO2 measurements or combinations of these data. The v10 OCO-2 MIP NCE estimates are combined with “bottom-up” estimates of fossil fuel emissions and lateral carbon fluxes to estimate changes in terrestrial carbon stocks, which are impacted by anthropogenic and natural drivers. These flux and stock change estimates are reported annually (2015–2020) as both a global 1∘ × 1∘ gridded dataset and a country-level dataset and are available for download from the Committee on Earth Observation Satellites' (CEOS) website: https://doi.org/10.48588/npf6-sw92 (Byrne et al., 2022). Across the v10 OCO-2 MIP experiments, we obtain increases in the ensemble median terrestrial carbon stocks of 3.29–4.58 Pg CO2 yr−1 (0.90–1.25 Pg C yr−1). This is a result of broad increases in terrestrial carbon stocks across the northern extratropics, while the tropics generally have stock losses but with considerable regional variability and differences between v10 OCO-2 MIP experiments. We discuss the state of the science for tracking emissions and removals using top-down methods, including current limitations and future developments towards top-down monitoring and verification systems.

Mössbauer nuclei feature exceptionally narrow resonances at hard x-ray energies, which render them ideal probes for structure and dynamics in condensed-matter systems, and a promising platform for x-ray quantum optics and fundamental tests. However, a direct spectroscopy at modern x-ray sources such as synchrotrons or xray free-electron lasers is challenging, because of the broad spectral bandwidth of the delivered x-ray pulses, and because of a limited spectral resolution offered by x-ray optics and detectors. To overcome these challenges, here, we propose a spectroscopy technique based on a spectrally narrow reference absorber that is rapidly oscillating along the propagation direction of the x-ray light. The motion induces sidebands to the response of the absorber, which we scan across the spectrum of the unknown target to gain spectral information. The oscillation further introduces a dependence of the detected light on the motional phase at the time of x-ray excitation as an additional controllable degree of freedom. We show how a Fourier analysis with respect to this phase enables one to selectively extract parts of the recorded intensity after the actual experiment, throughout the data analysis. This allows one to improve the spectral recovery by removing unwanted signal contributions. Our method is capable of gaining spectral information from the entire measured intensity, and not only from the intensity at late times after the excitation, such that a significantly higher part of the signal photons can be used. Furthermore, it not only enables one to measure the amplitude of the spectral response but also its phase.

Abstract. Accurate accounting of emissions and removals of CO2 is critical for the planning and verification of emission reduction targets in support of the Paris Agreement. Here, we present a pilot dataset of country-specific net carbon exchange (NCE; fossil plus terrestrial ecosystem fluxes) and terrestrial carbon stock changes aimed at informing countries’ carbon budgets. These estimates are based on "top-down" NCE outputs from the v10 Orbiting Carbon Observatory (OCO-2) modeling intercomparison project (MIP), wherein an ensemble of inverse modeling groups conducted standardized experiments assimilating OCO-2 column-averaged dry-air mole fraction (XCO2) retrievals (ACOS v10), in situ CO2 measurements, or combinations of these data. The v10 OCO-2 MIP NCE estimates are combined with "bottom-up" estimates of fossil fuel emissions and lateral carbon fluxes to estimate changes in terrestrial carbon stocks, which are impacted by anthropogenic and natural drivers. These flux and stock change estimates are reported annually (2015–2020) as both a global 1° × 1° gridded dataset and as a country-level dataset. Across the v10 OCO-2 MIP experiments, we obtain increases in the ensemble median terrestrial carbon stocks of 3.29–4.58 PgCO2 yr-1 (0.90–1.25 PgC yr-1). This is a result of broad increases in terrestrial carbon stocks across the northern extratropics, while the tropics generally have stock losses but with considerable regional variability and differences between v10 OCO-2 MIP experiments. We discuss the state of the science for tracking emissions and removals using top-down methods, including current limitations and future developments towards top-down monitoring and verification systems.

Recent advances in satellite observations of methane provide increased opportunities for inverse modeling. However, challenges exist in the satellite observation optimization and retrievals for high latitudes. In this study, we examine possibilities and challenges in the use of the total column averaged dry-air mole fractions of methane (XCH4) data over land from the TROPOspheric Monitoring Instrument (TROPOMI) on board the Sentinel 5 Precursor satellite in the estimation of CH4 fluxes using the CarbonTracker Europe-CH4 (CTE-CH4) atmospheric inverse model. We carry out simulations assimilating two retrieval products: Netherlands Institute for Space Research’s (SRON) operational and University of Bremen’s Weighting Function Modified Differential Optical Absorption Spectroscopy (WFM-DOAS). For comparison, we also carry out a simulation assimilating the ground-based surface data. Our results show smaller regional emissions in the TROPOMI inversions compared to the prior and surface inversion, although they are roughly within the range of the previous studies. The wetland emissions in summer and anthropogenic emissions in spring are lesser. The inversion results based on the two satellite datasets show many similarities in terms of spatial distribution and time series but also clear differences, especially in Canada, where CH4 emission maximum is later, when the SRON’s operational data are assimilated. The TROPOMI inversions show higher CH4 emissions from oil and gas production and coal mining from Russia and Kazakhstan. The location of hotspots in the TROPOMI inversions did not change compared to the prior, but all inversions indicated spatially more homogeneous high wetland emissions in northern Fennoscandia. In addition, we find that the regional monthly wetland emissions in the TROPOMI inversions do not correlate with the anthropogenic emissions as strongly as those in the surface inversion. The uncertainty estimates in the TROPOMI inversions are more homogeneous in space, and the regional uncertainties are comparable to the surface inversion. This indicates the potential of the TROPOMI data to better separately estimate wetland and anthropogenic emissions, as well as constrain spatial distributions. This study emphasizes the importance of quantifying and taking into account the model and retrieval uncertainties in regional levels in order to improve and derive more robust emission estimates.

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