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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: orcid M. Saunois;
    M. Saunois
    ORCID
    Harvested from ORCID Public Data File

    M. Saunois in OpenAIRE
    orcid P. Bousquet;
    P. Bousquet
    ORCID
    Harvested from ORCID Public Data File

    P. Bousquet in OpenAIRE
    orcid B. Poulter;
    B. Poulter
    ORCID
    Harvested from ORCID Public Data File

    B. Poulter in OpenAIRE
    orcid A. Peregon;
    A. Peregon
    ORCID
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    A. Peregon in OpenAIRE
    +78 Authors

    Abstract. Following the recent Global Carbon Project (GCP) synthesis of the decadal methane (CH4) budget over 2000–2012 (Saunois et al., 2016), we analyse here the same dataset with a focus on quasi-decadal and inter-annual variability in CH4 emissions. The GCP dataset integrates results from top-down studies (exploiting atmospheric observations within an atmospheric inverse-modelling framework) and bottom-up models (including process-based models for estimating land surface emissions and atmospheric chemistry), inventories of anthropogenic emissions, and data-driven approaches. The annual global methane emissions from top-down studies, which by construction match the observed methane growth rate within their uncertainties, all show an increase in total methane emissions over the period 2000–2012, but this increase is not linear over the 13 years. Despite differences between individual studies, the mean emission anomaly of the top-down ensemble shows no significant trend in total methane emissions over the period 2000–2006, during the plateau of atmospheric methane mole fractions, and also over the period 2008–2012, during the renewed atmospheric methane increase. However, the top-down ensemble mean produces an emission shift between 2006 and 2008, leading to 22 [16–32] Tg CH4 yr−1 higher methane emissions over the period 2008–2012 compared to 2002–2006. This emission increase mostly originated from the tropics, with a smaller contribution from mid-latitudes and no significant change from boreal regions. The regional contributions remain uncertain in top-down studies. Tropical South America and South and East Asia seem to contribute the most to the emission increase in the tropics. However, these two regions have only limited atmospheric measurements and remain therefore poorly constrained. The sectorial partitioning of this emission increase between the periods 2002–2006 and 2008–2012 differs from one atmospheric inversion study to another. However, all top-down studies suggest smaller changes in fossil fuel emissions (from oil, gas, and coal industries) compared to the mean of the bottom-up inventories included in this study. This difference is partly driven by a smaller emission change in China from the top-down studies compared to the estimate in the Emission Database for Global Atmospheric Research (EDGARv4.2) inventory, which should be revised to smaller values in a near future. We apply isotopic signatures to the emission changes estimated for individual studies based on five emission sectors and find that for six individual top-down studies (out of eight) the average isotopic signature of the emission changes is not consistent with the observed change in atmospheric 13CH4. However, the partitioning in emission change derived from the ensemble mean is consistent with this isotopic constraint. At the global scale, the top-down ensemble mean suggests that the dominant contribution to the resumed atmospheric CH4 growth after 2006 comes from microbial sources (more from agriculture and waste sectors than from natural wetlands), with an uncertain but smaller contribution from fossil CH4 emissions. In addition, a decrease in biomass burning emissions (in agreement with the biomass burning emission databases) makes the balance of sources consistent with atmospheric 13CH4 observations. In most of the top-down studies included here, OH concentrations are considered constant over the years (seasonal variations but without any inter-annual variability). As a result, the methane loss (in particular through OH oxidation) varies mainly through the change in methane concentrations and not its oxidants. For these reasons, changes in the methane loss could not be properly investigated in this study, although it may play a significant role in the recent atmospheric methane changes as briefly discussed at the end of the paper.

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    CORE
    Article . 2017
    License: CC BY
    Data sources: CORE
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    OceanRep
    Article . 2017 . Peer-reviewed
    Data sources: OceanRep
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    Atmospheric Chemistry and Physics (ACP)
    Article . 2017 . Peer-reviewed
    License: CC BY
    Data sources: Crossref
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    Atmospheric Chemistry and Physics (ACP)
    Article
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    Data sources: UnpayWall
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    https://doi.org/10.5194/acp-20...
    Article . 2017 . Peer-reviewed
    License: CC BY
    Data sources: Crossref
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    https://www.atmos-chem-phys.ne...
    Article
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    MPG.PuRe
    Article . 2017
    License: CC BY
    Data sources: MPG.PuRe
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    HAL-IRD
    Article . 2017
    License: CC BY
    Data sources: HAL-IRD
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    HAL-UPMC
    Article . 2017
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    HAL-Ecole des Ponts ParisTech
    Article . 2017
    License: CC BY
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    HAL AMU
    Article . 2017
    License: CC BY
    Data sources: HAL AMU
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    HAL-CEA
    Article . 2017
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    HAL-INSU
    Article . 2017
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    HAL INRAE
    Article . 2017
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    Data sources: HAL INRAE
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    Munin - Open Research Archive
    Article . 2017 . Peer-reviewed
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    DSpace@MIT
    Article . 2017
    License: CC BY
    Data sources: DSpace@MIT
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    https://dx.doi.org/10.60692/xh...
    Other literature type . 2017
    Data sources: Datacite
    https://dx.doi.org/10.60692/2h...
    Other literature type . 2017
    Data sources: Datacite
    Copernicus Publications
    Other literature type . 2018
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      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/ COREarrow_drop_down
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      CORE
      Article . 2017
      License: CC BY
      Data sources: CORE
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      OceanRep
      Article . 2017 . Peer-reviewed
      Data sources: OceanRep
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      Atmospheric Chemistry and Physics (ACP)
      Article . 2017 . Peer-reviewed
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      Atmospheric Chemistry and Physics (ACP)
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      MPG.PuRe
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      Munin - Open Research Archive
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      https://dx.doi.org/10.60692/xh...
      Other literature type . 2017
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      https://dx.doi.org/10.60692/2h...
      Other literature type . 2017
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      Copernicus Publications
      Other literature type . 2018
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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: orcid Minde An;
    Minde An
    ORCID
    Harvested from ORCID Public Data File

    Minde An in OpenAIRE
    orcid Ronald G. Prinn;
    Ronald G. Prinn
    ORCID
    Harvested from ORCID Public Data File

    Ronald G. Prinn in OpenAIRE
    orcid Luke M. Western;
    Luke M. Western
    ORCID
    Harvested from ORCID Public Data File

    Luke M. Western in OpenAIRE
    orcid bw Xingchen Zhao;
    Xingchen Zhao
    ORCID
    Derived by OpenAIRE algorithms or harvested from 3rd party repositories

    Xingchen Zhao in OpenAIRE
    +9 Authors

    AbstractSulfur hexafluoride (SF6) is a potent greenhouse gas. Here we use long-term atmospheric observations to determine SF6 emissions from China between 2011 and 2021, which are used to evaluate the Chinese national SF6 emission inventory and to better understand the global SF6 budget. SF6 emissions in China substantially increased from 2.6 (2.3-2.7, 68% uncertainty) Gg yr−1 in 2011 to 5.1 (4.8-5.4) Gg yr−1 in 2021. The increase from China is larger than the global total emissions rise, implying that it has offset falling emissions from other countries. Emissions in the less-populated western regions of China, which have potentially not been well quantified in previous measurement-based estimates, contribute significantly to the national SF6 emissions, likely due to substantial power generation and transmission in that area. The CO2-eq emissions of SF6 in China in 2021 were 125 (117-132) million tonnes (Mt), comparable to the national total CO2 emissions of several countries such as the Netherlands or Nigeria. The increasing SF6 emissions offset some of the CO2 reductions achieved through transitioning to renewable energy in the power industry, and might hinder progress towards achieving China’s goal of carbon neutrality by 2060 if no concrete control measures are implemented.

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    Nature Communications
    Article . 2024 . Peer-reviewed
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    PubMed Central
    Other literature type . 2024
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    Data sources: PubMed Central
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    Nature Communications
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    Nature Communications
    Article . 2024 . Peer-reviewed
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    https://dx.doi.org/10.60692/rv...
    Other literature type . 2024
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    https://dx.doi.org/10.60692/hx...
    Other literature type . 2024
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      Nature Communications
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      PubMed Central
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      Nature Communications
      Article . 2024
      Data sources: DOAJ
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      Nature Communications
      Article . 2024 . Peer-reviewed
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      https://dx.doi.org/10.60692/rv...
      Other literature type . 2024
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      https://dx.doi.org/10.60692/hx...
      Other literature type . 2024
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    Authors: orcid Lunt, Mark F;
    Lunt, Mark F
    ORCID
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    Lunt, Mark F in OpenAIRE
    orcid Rigby, Matthew;
    Rigby, Matthew
    ORCID
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    Rigby, Matthew in OpenAIRE
    orcid Ganesan, Anita L;
    Ganesan, Anita L
    ORCID
    Harvested from ORCID Public Data File

    Ganesan, Anita L in OpenAIRE
    Manning, Alistair J; +23 Authors

    Significance Hydrofluorocarbons (HFCs) are among the atmosphere’s fastest growing, and most potent, greenhouse gases. Proposals have been made to phase down their use over the coming decades. Such initiatives may largely be informed by existing emissions inventories, which, we show, are the subject of significant uncertainty. In this work, we use atmospheric models and measurements to examine the accuracy of these inventories for five major HFCs. We show that, when aggregated together, reported emissions of these HFCs from developed countries are consistent with the atmospheric measurements, and almost half of global emissions now originate from nonreporting countries. However, the agreement between our results and the inventory breaks down for individual HFC emissions, suggesting inaccuracies in the reporting methods for individual compounds.

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    Authors: orcid Hope A. Michelsen;
    Hope A. Michelsen
    ORCID
    Harvested from ORCID Public Data File

    Hope A. Michelsen in OpenAIRE
    Ray P. Bambha; orcid Mixtli Campos-Pineda;
    Mixtli Campos-Pineda
    ORCID
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    Mixtli Campos-Pineda in OpenAIRE
    Ralph F. Keeling; +17 Authors

    AbstractWe present an analysis of methane (CH4) emissions using atmospheric observations from 13 sites in California during June 2013 to May 2014. A hierarchical Bayesian inversion method is used to estimate CH4 emissions for spatial regions (0.3° pixels for major regions) by comparing measured CH4 mixing ratios with transport model (Weather Research and Forecasting and Stochastic Time‐Inverted Lagrangian Transport) predictions based on seasonally varying California‐specific CH4 prior emission models. The transport model is assessed using a combination of meteorological and carbon monoxide (CO) measurements coupled with the gridded California Air Resources Board (CARB) CO emission inventory. The hierarchical Bayesian inversion suggests that state annual anthropogenic CH4 emissions are 2.42 ± 0.49 Tg CH4/yr (at 95% confidence), higher (1.2–1.8 times) than the current CARB inventory (1.64 Tg CH4/yr in 2013). It should be noted that undiagnosed sources of errors or uncaptured errors in the model‐measurement mismatch covariance may increase these uncertainty bounds beyond that indicated here. The CH4 emissions from the Central Valley and urban regions (San Francisco Bay and South Coast Air Basins) account for ~58% and 26% of the total posterior emissions, respectively. This study suggests that the livestock sector is likely the major contributor to the state total CH4 emissions, in agreement with CARB's inventory. Attribution to source sectors for subregions of California using additional trace gas species would further improve the quantification of California's CH4 emissions and mitigation efforts toward the California Global Warming Solutions Act of 2006 (Assembly Bill 32).

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    Journal of Geophysical Research Atmospheres
    Article . 2016 . Peer-reviewed
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      Journal of Geophysical Research Atmospheres
      Article . 2016 . Peer-reviewed
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    Authors: Norbert Schmidbauer; orcid Ronald G. Prinn;
    Ronald G. Prinn
    ORCID
    Harvested from ORCID Public Data File

    Ronald G. Prinn in OpenAIRE
    Chris Rene Lunder; Jian Yu Huang; +24 Authors

    Ground‐based in situ measurements of 1,1‐difluoroethane (HFC‐152a, CH3CHF2) which is regulated under the Kyoto Protocol are reported under the auspices of the AGAGE (Advanced Global Atmospheric Gases Experiment) and SOGE (System of Observation of halogenated Greenhouse gases in Europe) programs. Observations of HFC‐152a at five locations (four European and one Australian) over a 10 year period were recorded. The annual average growth rate of HFC‐152a in the midlatitude Northern Hemisphere has risen from 0.11 ppt/yr to 0.6 ppt/yr from 1994 to 2004. The Southern Hemisphere annual average growth rate has risen from 0.09 ppt/yr to 0.4 ppt/yr from 1998 to 2004. The 2004 average mixing ratio for HFC‐152a was 5.0 ppt and 1.8 ppt in the Northern and Southern hemispheres, respectively. The annual cycle observed for this species in both hemispheres is approximately consistent with measured annual cycles at the same locations in other gases which are destroyed by OH. Yearly global emissions of HFC‐152a from 1994 to 2004 are derived using the global mean HFC‐152a observations and a 12‐box 2‐D model. The global emission of HFC‐152a has risen from 7 Kt/yr to 28 Kt/yr from 1995 to 2004. On the basis of observations of above‐baseline elevations in the HFC‐152a record and a consumption model, regional emission estimates for Europe and Australia are calculated, indicating accelerating emissions from Europe since 2000. The overall European emission in 2004 ranges from 1.5 to 4.0 Kt/year, 5–15% of global emissions for 1,1‐difluoroethane, while the Australian contribution is negligible at 5–10 tonnes/year, <0.05% of global emissions.

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    Journal of Geophysical Research Atmospheres
    Article . 2007 . Peer-reviewed
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    IRIS Cnr
    Article . 2007
    Data sources: IRIS Cnr
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      Journal of Geophysical Research Atmospheres
      Article . 2007 . Peer-reviewed
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    Authors: orcid B. D. Hall;
    B. D. Hall
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    B. D. Hall in OpenAIRE
    orcid A. Engel;
    A. Engel
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    A. Engel in OpenAIRE
    orcid J. Mühle;
    J. Mühle
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    J. Mühle in OpenAIRE
    J. W. Elkins; +23 Authors

    Abstract. The International Halocarbons in Air Comparison Experiment (IHALACE) was conducted to document relationships between calibration scales among various laboratories that measure atmospheric greenhouse and ozone depleting gases. This study included trace gases such as chlorofluorocarbons (CFCs), hydrochlorofluorocarbons (HCFCs), and hydrofluorocarbons (HFCs), as well as nitrous oxide, methane, sulfur hexafluoride, very short-lived halocompounds, and carbonyl sulfide. Many of these gases are present in the unpolluted atmosphere at pmol mol−1 (parts per trillion) or nmol mol−1 (parts per billion) levels. Six stainless steel cylinders containing natural and modified natural air samples were circulated among 19 laboratories. Results from this experiment reveal relatively good agreement (within a few percent) among commonly used calibration scales. Scale relationships for some gases, such as CFC-12 and CCl4, were found to be consistent with those derived from estimates of global mean mole fractions, while others, such as halon-1211 and CH3Br, revealed discrepancies. The transfer of calibration scales among laboratories was problematic in many cases, meaning that measurements tied to a particular scale may not, in fact, be compatible. Large scale transfer errors were observed for CH3CCl3 (10–100%) and CCl4 (2–30%), while much smaller scale transfer errors (< 1%) were observed for halon-1211, HCFC-22, and HCFC-142b. These results reveal substantial improvements in calibration over previous comparisons. However, there is room for improvement in communication and coordination of calibration activities with respect to the measurement of halogenated and related trace gases.

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    Atmospheric Measurement Techniques (AMT)
    Article . 2014 . Peer-reviewed
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    Atmospheric Measurement Techniques (AMT)
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    https://doi.org/10.5194/amtd-6...
    Article . 2013 . Peer-reviewed
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    https://doi.org/10.5194/amt-7-...
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    https://dx.doi.org/10.5445/ir/...
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    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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    Article . 2014 . Peer-reviewed
    Data sources: SNSF P3 Database
    image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    http://www.atmos-meas-tech-dis...
    Article . 2013 . Peer-reviewed
    Data sources: SNSF P3 Database
    image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
    Copernicus Publications
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      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/ University of Califo...arrow_drop_down
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      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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      Article . 2014 . Peer-reviewed
      License: CC BY
      Data sources: Crossref
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      Data sources: UnpayWall
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      Article . 2013 . Peer-reviewed
      License: CC BY
      Data sources: Crossref
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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      Article . 2014
      License: CC BY
      Data sources: Datacite
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
      http://www.atmos-meas-tech.net...
      Article . 2014 . Peer-reviewed
      Data sources: SNSF P3 Database
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
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      Article . 2013 . Peer-reviewed
      Data sources: SNSF P3 Database
      image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
      Copernicus Publications
      Other literature type . 2018
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