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A comprehensive quantification of global nitrous oxide sources and sinks

Naturevolume 586pages248–256 (2020)Cite this article

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Abstract

Nitrous oxide (N2O), like carbon dioxide, is a long-lived greenhouse gas that accumulates in the atmosphere. Over the past 150 years, increasing atmospheric N2O concentrations have contributed to stratospheric ozone depletion1 and climate change2, with the current rate of increase estimated at 2 per cent per decade. Existing national inventories do not provide a full picture of N2O emissions, owing to their omission of natural sources and limitations in methodology for attributing anthropogenic sources. Here we present a global N2O inventory that incorporates both natural and anthropogenic sources and accounts for the interaction between nitrogen additions and the biochemical processes that control N2O emissions. We use bottom-up (inventory, statistical extrapolation of flux measurements, process-based land and ocean modelling) and top-down (atmospheric inversion) approaches to provide a comprehensive quantification of global N2O sources and sinks resulting from 21 natural and human sectors between 1980 and 2016. Global N2O emissions were 17.0 (minimum–maximum estimates: 12.2–23.5) teragrams of nitrogen per year (bottom-up) and 16.9 (15.9–17.7) teragrams of nitrogen per year (top-down) between 2007 and 2016. Global human-induced emissions, which are dominated by nitrogen additions to croplands, increased by 30% over the past four decades to 7.3 (4.2–11.4) teragrams of nitrogen per year. This increase was mainly responsible for the growth in the atmospheric burden. Our findings point to growing N2O emissions in emerging economies—particularly Brazil, China and India. Analysis of process-based model estimates reveals an emerging N2O–climate feedback resulting from interactions between nitrogen additions and climate change. The recent growth in N2O emissions exceeds some of the highest projected emission scenarios3,4, underscoring the urgency to mitigate N2O emissions.

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Fig. 1: Global N2O budget for 2007–2016.
Fig. 2: Regional N2O sources in the decade 2007–2016.
Fig. 3: Ensembles of regional anthropogenic N2O emissions over the period 1980–2016.
Fig. 4: Historical and projected global anthropogenic N2O emissions and concentrations.

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Data availability

The relevant datasets of this study are archived in the box site of the International Center for Climate and Global Change Research at Auburn University (https://auburn.box.com/). Researchers that are interested in using the results made available in the repository are encouraged to contact the original data providers.

Code availability

The relevant codes used in this study are archived in the box site of the International Center for Climate and Global Change Research at Auburn University (https://auburn.box.com/).

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Acknowledgements

This paper is the result of a collaborative international effort under the umbrella of the Global Carbon Project (a project of Future Earth and a research partner of the World Climate Research Programme) and International Nitrogen Initiative. This research was made possible partly by Andrew Carnegie Fellowship award no. G-F-19-56910; NSF grant nos 1903722,1243232 and 1922687; NASA grant nos NNX14AO73G, NNX10AU06G, NNX11AD47G and NNX14AF93G; NOAA grant nos NA16NOS4780207 and NA16NOS4780204; National Key R&D Program of China (grant no. 2017YFA0604702); National Natural Science Foundation of China (grant no. 41961124006); and OUC-AU Joint Center Program. E.T.B., P.R., G.P.P., R.L.T. and P.S. acknowledge funding support from VERIFY project (EC H2020 grant no. 776810); P.S. also acknowledges funding from the EC H2020 grant no. 641816 (CRESCENDO); A.I. acknowledges funding support from JSPS KAKENHI grant (no. 17H01867); G.B., F.J. and S.L. acknowledge support from the Swiss National Science Foundation (no. 200020_172476) and EC H2020 grant no. 821003 (Project 4C) and no. 820989 (Project COMFORT); A.L. acknowledges support from DFG project SFB754/3; S.Z. acknowledges support from EC H2020 grant no. 647204; K.C.W. and D.B.M. acknowledge support from NASA (IDS grant no. NNX17AK18G) and NOAA (grant no. NA13OAR4310086); P.A.R. acknowledges NASA Award NNX17AI74G; M.M. acknowledges support from the Scottish Government’s Rural and Environment Science and Analytical Services Division (RESAS) Environmental Change Programme (2016-2021); B.D.E. acknowledges the support from ARC Linkage Grants LP150100519 and LP190100271; M.J.P. acknowledges the US Department of Energy grant no. DE-SC0012536, Lawrence Livermore National Laboratory B628407 and NASA MAP program grant no. NNX13AL12G; S.B. was supported by the EC H2020 with the CRESCENDO project (grant no. 641816) and by the COMFORT project (grant no. 820989), and also acknowledges the support of the team in charge of the CNRM-CM climate model; F.Z. acknowledges the support from the National Natural Science Foundation of China (41671464). Supercomputing time was provided by the Météo-France/DSI supercomputing center. P.K.P. is partly supported by Environment Research and Technology Development Fund (#2-1802) of the Ministry of the Environment, Japan; R.L. acknowledges support from the French state aid managed by the ANR under the ‘Investissements d’avenir’ programme with the reference ANR-16-CONV-0003. NOAA ground-based observations of atmospheric N2O are supported by NOAA’s Climate Program Office under the Atmospheric Chemistry Carbon Cycle and Climate (AC4) theme. The AGAGE stations measuring N2O are supported by NASA (USA) grants NNX16AC98G to MIT and NNX16AC97G and NNX16AC96G to SIO, and by BEIS (UK) for Mace Head, NOAA (USA) for Barbados, and CSIRO and BoM (Australia) for Cape Grim. F.N.T. acknowledges funding from FAO regular programme. The views expressed in this publication are those of the author(s) and do not necessarily reflect the views or policies of FAO. P.C. acknowledges support from ERC Synergy Grant Imbalance-P and the ANR Cland Convergence Institute. We also thank S. Frolking for constructive comments and suggestions that have helped to improve this paper. The statements made and views expressed are solely the responsibility of the authors.

Author information

Authors and Affiliations

  1. International Center for Climate and Global Change Research, School of Forestry and Wildlife Sciences, Auburn University, Auburn, AL, USA

    Hanqin Tian, Rongting Xu, Naiqing Pan, Shufen Pan, Hao Shi & Yuanzhi Yao

  2. Global Carbon Project, CSIRO Oceans and Atmosphere, Canberra, Australian Capital Territory, Australia

    Josep G. Canadell

  3. Norsk Institutt for Luftforskning, NILU, Kjeller, Norway

    Rona L. Thompson

  4. International Institute for Applied Systems Analysis, Laxenburg, Austria

    Wilfried Winiwarter

  5. Institute of Environmental Engineering, University of Zielona Góra, Zielona Góra, Poland

    Wilfried Winiwarter

  6. School of Environmental Sciences, University of East Anglia, Norwich, UK

    Parvadha Suntharalingam & Erik T. Buitenhuis

  7. Appalachian Laboratory, University of Maryland Center for Environmental Science, Frostburg, MD, USA

    Eric A. Davidson

  8. Laboratoire des Sciences du Climat et de l’Environnement, LSCE, CEA CNRS, UVSQ UPSACLAY, Gif sur Yvette, France

    Philippe Ciais, Jinfeng Chang, Ronny Lauerwald, Wei Li & Nicolas Vuichard

  9. Department of Earth System Science, Stanford University, Stanford, CA, USA

    Robert B. Jackson

  10. Woods Institute for the Environment, Stanford University, Stanford, CA, USA

    Robert B. Jackson

  11. Precourt Institute for Energy, Stanford University, Stanford, CA, USA

    Robert B. Jackson

  12. European Commission, Joint Research Centre (JRC), Ispra, Italy

    Greet Janssens-Maenhout

  13. Ghent University, Faculty of Engineering and Architecture, Ghent, Belgium

    Greet Janssens-Maenhout

  14. Department of Earth System Science, University of California Irvine, Irvine, CA, USA

    Michael J. Prather & Daniel J. Ruiz

  15. Department of Geoscience, Environment & Society, Université Libre de Bruxelles, Brussels, Belgium

    Pierre Regnier, Goulven G. Laruelle & Ronny Lauerwald

  16. State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China

    Naiqing Pan & Bojie Fu

  17. CICERO Center for International Climate Research, Oslo, Norway

    Glen P. Peters

  18. Statistics Division, Food and Agriculture Organization of the United Nations, Rome, Italy

    Francesco N. Tubiello

  19. Max Planck Institute for Biogeochemistry, Jena, Germany

    Sönke Zaehle

  20. Sino-France Institute of Earth Systems Science, Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing, China

    Feng Zhou

  21. Karlsruhe Institute of Technology, Institute of Meteorology and Climate Research/Atmospheric Environmental Research, Garmisch-Partenkirchen, Germany

    Almut Arneth

  22. Climate and Environmental Physics, Physics Institute and Oeschger Centre for Climate Change Research, University of Bern, Bern, Switzerland

    Gianna Battaglia, Fortunat Joos & Sebastian Lienert

  23. Centre National de Recherches Météorologiques (CNRM), Université de Toulouse, Météo-France, CNRS, Toulouse, France

    Sarah Berthet

  24. LMD-IPSL, Ecole Normale Supérieure / PSL Université, CNRS, Ecole Polytechnique, Sorbonne Université, Paris, France

    Laurent Bopp

  25. PBL Netherlands Environmental Assessment Agency, The Hague, The Netherlands

    Alexander F. Bouwman

  26. Department of Earth Sciences – Geochemistry, Faculty of Geosciences, Utrecht University, Utrecht, The Netherlands

    Alexander F. Bouwman

  27. Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao, China

    Alexander F. Bouwman & Junjie Wang

  28. Tyndall Centre for Climate Change Research, School of Environmental Sciences, University of East Anglia, Norwich, UK

    Erik T. Buitenhuis

  29. College of Environmental and Resource Sciences, Zhejiang University, Hangzhou, China

    Jinfeng Chang

  30. National Centre for Earth Observation, University of Leeds, Leeds, UK

    Martyn P. Chipperfield & Chris Wilson

  31. Institute for Climate and Atmospheric Science, School of Earth and Environment, University of Leeds, Leeds, UK

    Martyn P. Chipperfield & Chris Wilson

  32. Woods Hole Research Center, Falmouth, MA, USA

    Shree R. S. Dangal

  33. NOAA Global Monitoring Laboratory, Boulder, CO, USA

    Edward Dlugokencky, James W. Elkins & Bradley Hall

  34. Centre for Coastal Biogeochemistry, School of Environment Science and Engineering, Southern Cross University, Lismore, New South Wales, Australia

    Bradley D. Eyre

  35. Faculty of Geographical Science, Beijing Normal University, Beijing, China

    Bojie Fu

  36. Center for Global Environmental Research, National Institute for Environmental Studies, Tsukuba, Japan

    Akihiko Ito

  37. Climate Science Centre, CSIRO Oceans and Atmosphere, Aspendale, Victoria, Australia

    Paul B. Krummel

  38. GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany

    Angela Landolfi

  39. Istituto di Scienze Marine, Consiglio Nazionale delle Ricerche (CNR), Rome, Italy

    Angela Landolfi

  40. Université Paris-Saclay, INRAE, AgroParisTech, UMR ECOSYS, Thiverval-Grignon, France

    Ronny Lauerwald

  41. Ministry of Education Key Laboratory for Earth System Modeling, Department of Earth System Science, Tsinghua University, Beijing, China

    Wei Li

  42. Yale School of Forestry and Environmental Studies, New Haven, CT, USA

    Taylor Maavara & Peter A. Raymond

  43. Land Economy, Environment & Society, Scotland’s Rural College (SRUC), Edinburgh, UK

    Michael MacLeod

  44. Department of Soil, Water, and Climate, University of Minnesota, St Paul, MN, USA

    Dylan B. Millet & Kelley C. Wells

  45. Department of Physical Geography and Ecosystem Science, Lund University, Lund, Sweden

    Stefan Olin

  46. Research Institute for Global Change, JAMSTEC, Yokohama, Japan

    Prabir K. Patra

  47. Center for Environmental Remote Sensing, Chiba University, Chiba, Japan

    Prabir K. Patra

  48. Center for Global Change Science, Massachusetts Institute of Technology, Cambridge, MA, USA

    Ronald G. Prinn

  49. Faculty of Science, Vrije Universiteit, Amsterdam, The Netherlands

    Guido R. van der Werf

  50. Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA, USA

    Ray F. Weiss

  51. Department of Forestry, Mississippi State University, Mississippi State, MS, USA

    Jia Yang

Authors
  1. Hanqin Tian
  2. Rongting Xu
  3. Josep G. Canadell
  4. Rona L. Thompson
  5. Wilfried Winiwarter
  6. Parvadha Suntharalingam
  7. Eric A. Davidson
  8. Philippe Ciais
  9. Robert B. Jackson
  10. Greet Janssens-Maenhout
  11. Michael J. Prather
  12. Pierre Regnier
  13. Naiqing Pan
  14. Shufen Pan
  15. Glen P. Peters
  16. Hao Shi
  17. Francesco N. Tubiello
  18. Sönke Zaehle
  19. Feng Zhou
  20. Almut Arneth
  21. Gianna Battaglia
  22. Sarah Berthet
  23. Laurent Bopp
  24. Alexander F. Bouwman
  25. Erik T. Buitenhuis
  26. Jinfeng Chang
  27. Martyn P. Chipperfield
  28. Shree R. S. Dangal
  29. Edward Dlugokencky
  30. James W. Elkins
  31. Bradley D. Eyre
  32. Bojie Fu
  33. Bradley Hall
  34. Akihiko Ito
  35. Fortunat Joos
  36. Paul B. Krummel
  37. Angela Landolfi
  38. Goulven G. Laruelle
  39. Ronny Lauerwald
  40. Wei Li
  41. Sebastian Lienert
  42. Taylor Maavara
  43. Michael MacLeod
  44. Dylan B. Millet
  45. Stefan Olin
  46. Prabir K. Patra
  47. Ronald G. Prinn
  48. Peter A. Raymond
  49. Daniel J. Ruiz
  50. Guido R. van der Werf
  51. Nicolas Vuichard
  52. Junjie Wang
  53. Ray F. Weiss
  54. Kelley C. Wells
  55. Chris Wilson
  56. Jia Yang
  57. Yuanzhi Yao

Contributions

H.T., R.L.T., J.G.C. and R.B.J. designed and coordinated the study. H.T., R.X., J.G.C., R.L.T., W.W., P.S., E.A.D., P.C., R.B.J., G.J.-M., M.J.P., N.P., S.P., P.R., H.S., F.N.T., S.Z., F.Z., B.F. and G.P.P. conducted data analysis, synthesis and wrote the paper. R.L.T. led atmospheric inversions teaming with M.P.C., D.B.M., P.K.P., K.C.W. and C.W.; H.T. led land biosphere modelling teaming with P.C., H.S., S.Z., A.A., F.J., J.C., S.R.S.D., A.I., W.L., S.L., S.O., N.V., E.A.D. and S.D.; P.S. led ocean biogeochemical modelling teaming with G.B., L.B., S.B., E.T.B., F.J. and A.L.; P.R. led inland water and coastal modelling and synthesis teaming with B.D.E., G.G.L., R.L., T.M., P.A.R., H.T. and Y.Y.; A.F.B., J.W. and M.M. provided data of N2O flux in aquaculture. G.R.v.d.W. and J.Y. provided data of N2O emissions from biomass burning. F.Z. provided cropland N2O flux data from a statistical model and field observations. G.J.M., F.N.T. and W.W. provided N2O inventory data. M.J.P. and D.J.R. provided data of stratospheric and tropospheric sinks. G.P.P. provided RCP and SSP scenarios data and analysis. B.H., E.D. and J.W.E. provided a global N2O monitoring dataset from NOAA/ESRL GMD. R.G.P. and R.F.W. provided a global N2O monitoring dataset from AGAGE stations. P.B.K. provided a global N2O monitoring dataset from CSIRO. All co-authors reviewed and commented on the manuscript.

Corresponding author

Correspondence toHanqin Tian.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Peer review informationNature thanks Steve Frolking, Arvin Mosier and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Extended data figures and tables

Extended Data Fig. 1 Global mean growth rates and atmospheric concentration of N2O.

Global mean growth rates (solid lines, during 1995–2017) and atmospheric N2O concentration (dashed lines, during 1980–2017) are from the AGAGE6 (green), NOAA5 (orange) and CSIRO (blue) networks. Global mean growth rates were calculated with annual time steps and are shown as 12-month moving averages. Growth rates are not calculated before 1995 owing to insufficient data and higher uncertainties on the measurements.

Extended Data Fig. 2 The methodology for data synthesis of the global N2O budget.

BU and TD represent bottom-up and top-down methods, respectively. The colour codes are the same as that used in Table1 and Figs.13. We use both approaches, including 22 bottom-up and five top-down estimates of N2O fluxes from land and oceans. For sources estimated by the bottom-up approach, we include six process-based terrestrial biosphere modelling studies16; five process-based ocean biogeochemical models99; one nutrient budget model30,60,61; five inland water modelling studies35,36,50,51,68; one statistical model SRNM based on spatial extrapolation of field measurements17; and four greenhouse-gas inventories: EDGAR v4.3.2100, FAOSTAT101, GAINS41, and GFED4s102. In addition, previous studies regarding estimates of surface sink58,73, lightning53,54, atmospheric production56,57,103, aquaculture31,62 and model-based tropospheric sink81 and observed stratospheric sink1 are included in the current synthesis.aRef.31 and ref.62 provide global aquaculture N2O emissions in 2013 and in 2009, respectively; and the nutrient budget model30,60,61 provides nitrogen flows in global freshwater and marine aquaculture over the period 1980–2016.bModel-based estimates of N2O emissions from inland and coastal waters include rivers and reservoirs35,36, lakes51, estuaries35, coastal zones (that is, seagrasses, mangroves, saltmarsh and intertidal saltmarsh)68 and coastal upwelling50.

Extended Data Fig. 3 Comparison of annual total N2O emissions at global and regional scales estimated by bottom-up and top-down approaches.

The blue lines represent the mean N2O emission from bottom-up methods and the shaded areas show minimum and maximum estimates; the gold lines represent the mean N2O emission from top-down methods and the shaded areas show minimum and maximum estimates.

Extended Data Fig. 4 Global agricultural N2O emissions.

a, Direct emission from agricultural soils associated with mineral fertilizer, manure and crop residue inputs, and cultivation of organic soils based on EDGAR v4.3.2, GAINS, FAOSTAT, NMIP/DLEM and SRNM/DLEM estimates. NMIP/DLEM or SRNM/DLEM indicates the combination of N2O emission estimated by NMIP or SRNM from croplands with N2O emission from intensively managed grassland (pasture) by estimated by DLEM.b, Direct emission from the global total area under permanent meadows and pasture, due to manure nitrogen deposition (left on pasture) based on EDGAR v4.3.2, FAOSTAT and GAINS estimates.c, Emission from manure management based on FAOSTAT, GAINS and EDGAR v4.3.2.d, Aquaculture N2O emission based on a nutrient budget model30, ref.31 and ref.62; the solid line represents the ‘best estimate’ that is the product of emission factor (1.8%) and nitrogen waste from aquaculture provided by the nutrient budget model; the dashed lines represent the minimum and maximum values.

Extended Data Fig. 5 Global N2O emission from other direct anthropogenic sources.

a, Emission from fossil fuel combustion based on EDGAR v4.3.2 and GAINS estimates.b, Emission from industry based on EDGAR v4.3.2 and GAINS estimates.c, Emission from waste and waste water based on EDGAR v4.3.2 and GAINS estimates.d, Emission from biomass burning based on FAOSTAT, DLEM, and GFED4s estimates.

Extended Data Fig. 6 Global N2O emissions from natural soils, inland and coastal waters and due to change in climate, atmospheric CO2 and nitrogen deposition.

a, Changes in global soil N2O fluxes due to changing CO2 and climate.b, Global natural soil N2O emissions without consideration of land use change (for example, deforestation) and without consideration of indirect anthropogenic effects via global change (that is, climate, increased CO2 and atmospheric nitrogen deposition). The estimates are based on NMIP estimates during 1980–2016 including six process-based land biosphere models. Here, we also subtracted the difference between including and not including emissions from secondary forests (that grow back after pasture or cropland abandonment) as part of natural soil emissions based on NMIP estimates. The solid lines represent the ensemble and dashed lines show the minimum and maximum values.c, Global anthropogenic N2O emission from inland waters, estuaries, coastal zones based on models (model-based), FAOSTAT, GAINS and EDGAR v4.3.2 estimates.d, Emission due to atmospheric nitrogen deposition on land based on NMIP, FAOSTAT/EDGAR v4.3.2 and GAINS/EDGAR v4.3.2. FAOSTAT/EDGAR v4.3.2 or GAINS/EDGAR v4.3.2 indicates the combination of agricultural source estimates from FAOSTAT or GAINS with non-agricultural source estimates from EDGAR v4.3.2. A process-based model DLEM36 and a mechanistic stochastic model35,51 were used to estimate N2O emission from inland waters and estuaries, whereas site-level emission rates of N2O were upscaled to estimate global N2O fluxes from the global seagrass area68.

Extended Data Fig. 7 Global N2O dynamics due to land cover changes.

The blue line represents the mean forest N2O reduction caused by the long-term effect of reduced mature forest area (that is, deforestation) and shaded areas show minimum and maximum estimates; the red line represents the mean N2O emission from the post-deforestation pulse effect (that is, crop/pasture N2O emissions from legacy nitrogen of previous forest soil, not accounting for new fertilizer nitrogen added to these crop/pasture lands) and shaded areas show minimum and maximum estimates; the grey line represents the mean net deforestation emission of N2O and shaded areas show minimum and maximum estimates.

Extended Data Fig. 8 Global simulated N2O emission anomaly due to climate effect and global annual land surface temperature anomaly during 1901–2016.

Global N2O emission anomalies are the ensemble of six process-based land biosphere models in NMIP. The temperature data were obtained from the CRU-NCEP v8 climate dataset (https://vesg.ipsl.upmc.fr).a, The correlation between average global annual land surface temperature and simulated N2O emissions (that is, the result of SE6 experiment in NMIP16) considering annual changes in climate but keeping all other factors (that is, nitrogen fertilizer, manure, NDEP, increased CO2 and land cover change) at the level of 1860.b, The correlation between average global annual land surface temperature and simulated N2O emissions (that is, the result of SE1 experiment in NMIP16) considering annual changes in all factors during 1860–2016.

Extended Data Fig. 9 Direct soil emissions and agricultural product trades in Brazil.

a, The red line shows the ensemble direct N2O emissions from livestock manure based on EDGAR v4.3.2, GAINS and FAOSTAT, the sum of ‘manure left on pasture’ and ‘manure management’. The grey columns show the amount of beef exported by Brazil.b, Orange line shows the ensemble direct N2O emissions from croplands due to nitrogen fertilization based on NMIP and SRNM. The grey columns show the amount of soybeans and corn exported by Brazil. Data regarding beef and cereal product exports were adapted from the ABIEC (beef) and FAOSTAT (soybean and corn) databases. Mmt yr−1 represents millions of metric tons per year.

Extended Data Fig. 10 A comparison of anthropogenic N2O emissions and atmospheric N2O concentrations in the unharmonized SSPs.

An extension of Fig.4, in which the emission and concentration data are the same as in Fig.4.a, Global anthropogenic N2O emissions;b, Global N2O concentrations. The unharmonized emissions from the Integrated Assessment Models (IAMs)104 show a large variation due to different input data and model assumptions. Comparison with Fig.4b, d illustrates the modifications to the IAM scenario data for use in CMIP6. All baseline scenarios (SSP 3−7.0 and SSP 5−8.5; without climate policy applied) are shown in grey regardless of the radiative forcing level they reach in 2100.

Supplementary information

Supplementary Information

This file contains Supporting Text, Supplementary Tables 1–19 and Supplementary Figures 1 and 2.

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Tian, H., Xu, R., Canadell, J.G.et al. A comprehensive quantification of global nitrous oxide sources and sinks.Nature586, 248–256 (2020). https://doi.org/10.1038/s41586-020-2780-0

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