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      Salinity causes widespread restriction of methane emissions from small inland waters

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          Abstract

          Inland waters are one of the largest natural sources of methane (CH 4), a potent greenhouse gas, but emissions models and estimates were developed for solute-poor ecosystems and may not apply to salt-rich inland waters. Here we combine field surveys and eddy covariance measurements to show that salinity constrains microbial CH 4 cycling through complex mechanisms, restricting aquatic emissions from one of the largest global hardwater regions (the Canadian Prairies). Existing models overestimated CH 4 emissions from ponds and wetlands by up to several orders of magnitude, with discrepancies linked to salinity. While not significant for rivers and larger lakes, salinity interacted with organic matter availability to shape CH 4 patterns in small lentic habitats. We estimate that excluding salinity leads to overestimation of emissions from small Canadian Prairie waterbodies by at least 81% ( ~ 1 Tg yr −1 CO 2 equivalent), a quantity comparable to other major national emissions sources. Our findings are consistent with patterns in other hardwater landscapes, likely leading to an overestimation of global lentic CH 4 emissions. Widespread salinization of inland waters may impact CH 4 cycling and should be considered in future projections of aquatic emissions.

          Abstract

          Small inland water bodies are widely seen as important sources of methane to the atmosphere. This study demonstrates that hardwater ecosystems emit less of this potent greenhouse gas than predicted due to complex biogeochemical controls

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          Updated world map of the Köppen-Geiger climate classification

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            The global abundance and size distribution of lakes, ponds, and impoundments

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              The Global Methane Budget 2000–2017

              Abstract. Understanding and quantifying the global methane (CH4) budget is important for assessing realistic pathways to mitigate climate change. Atmospheric emissions and concentrations of CH4 continue to increase, making CH4 the second most important human-influenced greenhouse gas in terms of climate forcing, after carbon dioxide (CO2). The relative importance of CH4 compared to CO2 depends on its shorter atmospheric lifetime, stronger warming potential, and variations in atmospheric growth rate over the past decade, the causes of which are still debated. Two major challenges in reducing uncertainties in the atmospheric growth rate arise from the variety of geographically overlapping CH4 sources and from the destruction of CH4 by short-lived hydroxyl radicals (OH). To address these challenges, we have established a consortium of multidisciplinary scientists under the umbrella of the Global Carbon Project to synthesize and stimulate new research aimed at improving and regularly updating the global methane budget. Following Saunois et al. (2016), we present here the second version of the living review paper dedicated to the decadal methane budget, integrating results of top-down studies (atmospheric observations within an atmospheric inverse-modelling framework) and bottom-up estimates (including process-based models for estimating land surface emissions and atmospheric chemistry, inventories of anthropogenic emissions, and data-driven extrapolations). For the 2008–2017 decade, global methane emissions are estimated by atmospheric inversions (a top-down approach) to be 576 Tg CH4 yr−1 (range 550–594, corresponding to the minimum and maximum estimates of the model ensemble). Of this total, 359 Tg CH4 yr−1 or ∼ 60 % is attributed to anthropogenic sources, that is emissions caused by direct human activity (i.e. anthropogenic emissions; range 336–376 Tg CH4 yr−1 or 50 %–65 %). The mean annual total emission for the new decade (2008–2017) is 29 Tg CH4 yr−1 larger than our estimate for the previous decade (2000–2009), and 24 Tg CH4 yr−1 larger than the one reported in the previous budget for 2003–2012 (Saunois et al., 2016). Since 2012, global CH4 emissions have been tracking the warmest scenarios assessed by the Intergovernmental Panel on Climate Change. Bottom-up methods suggest almost 30 % larger global emissions (737 Tg CH4 yr−1, range 594–881) than top-down inversion methods. Indeed, bottom-up estimates for natural sources such as natural wetlands, other inland water systems, and geological sources are higher than top-down estimates. The atmospheric constraints on the top-down budget suggest that at least some of these bottom-up emissions are overestimated. The latitudinal distribution of atmospheric observation-based emissions indicates a predominance of tropical emissions (∼ 65 % of the global budget, < 30∘ N) compared to mid-latitudes (∼ 30 %, 30–60∘ N) and high northern latitudes (∼ 4 %, 60–90∘ N). The most important source of uncertainty in the methane budget is attributable to natural emissions, especially those from wetlands and other inland waters. Some of our global source estimates are smaller than those in previously published budgets (Saunois et al., 2016; Kirschke et al., 2013). In particular wetland emissions are about 35 Tg CH4 yr−1 lower due to improved partition wetlands and other inland waters. Emissions from geological sources and wild animals are also found to be smaller by 7 Tg CH4 yr−1 by 8 Tg CH4 yr−1, respectively. However, the overall discrepancy between bottom-up and top-down estimates has been reduced by only 5 % compared to Saunois et al. (2016), due to a higher estimate of emissions from inland waters, highlighting the need for more detailed research on emissions factors. Priorities for improving the methane budget include (i) a global, high-resolution map of water-saturated soils and inundated areas emitting methane based on a robust classification of different types of emitting habitats; (ii) further development of process-based models for inland-water emissions; (iii) intensification of methane observations at local scales (e.g., FLUXNET-CH4 measurements) and urban-scale monitoring to constrain bottom-up land surface models, and at regional scales (surface networks and satellites) to constrain atmospheric inversions; (iv) improvements of transport models and the representation of photochemical sinks in top-down inversions; and (v) development of a 3D variational inversion system using isotopic and/or co-emitted species such as ethane to improve source partitioning. The data presented here can be downloaded from https://doi.org/10.18160/GCP-CH4-2019 (Saunois et al., 2020) and from the Global Carbon Project.
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                Author and article information

                Contributors
                matthew.bogard@uleth.ca
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                24 January 2024
                24 January 2024
                2024
                : 15
                : 717
                Affiliations
                [1 ]Department of Biological Sciences, University of Lethbridge, ( https://ror.org/044j76961) Lethbridge, AB Canada
                [2 ]Department of Biology, University of Regina, ( https://ror.org/03dzc0485) Regina, SK S4S 0A2 Canada
                [3 ]Institute of Environmental Change and Society, University of Regina, ( https://ror.org/03dzc0485) S4S 0A2 Regina, SK Canada
                [4 ]Institute for Wetland & Waterfowl Research, Ducks Unlimited Canada, ( https://ror.org/04p45sn64) PO Box 1160, R0C 2Z0 Stonewall, MB Canada
                [5 ]Limnology Laboratory, Department of Biology, University of Regina, ( https://ror.org/03dzc0485) Regina, SK S4S 0A2 Canada
                [6 ]Department of Geography, The University of British Columbia, ( https://ror.org/03rmrcq20) Vancouver, BC Canada
                [7 ]LEHNA, Université Claude Bernard Lyon 1, ( https://ror.org/029brtt94) 69622 Villeurbanne, Cedex France
                [8 ]Present Address: Department of Geography, McGill University, ( https://ror.org/01pxwe438) Montreal, QC Canada
                [9 ]Present Address: Department of Biogeochemical Integration, Max Planck Institute for Biogeochemistry, ( https://ror.org/051yxp643) Jena, Germany
                Author information
                http://orcid.org/0000-0003-1985-7672
                http://orcid.org/0000-0001-9491-0328
                http://orcid.org/0000-0001-6835-8832
                http://orcid.org/0000-0003-1505-8427
                http://orcid.org/0000-0001-9805-9307
                http://orcid.org/0000-0002-2615-2040
                Article
                44715
                10.1038/s41467-024-44715-3
                10808391
                38267478
                d4fbe435-3b3f-4594-bcb6-dd1e074b3595
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 28 February 2023
                : 2 January 2024
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                © Springer Nature Limited 2024

                Uncategorized
                carbon cycle,ecosystem ecology,limnology,geochemistry
                Uncategorized
                carbon cycle, ecosystem ecology, limnology, geochemistry

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