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Abstract Large stocks of soil carbon (C) and nitrogen (N) in northern permafrost soils are vulnerable to remobilization under climate change. However, there are large uncertainties in present‐day greenhouse gas (GHG) budgets. We compare bottom‐up (data‐driven upscaling and process‐based models) and top‐down (atmospheric inversion models) budgets of carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) as well as lateral fluxes of C and N across the region over 2000–2020. Bottom‐up approaches estimate higher land‐to‐atmosphere fluxes for all GHGs. Both bottom‐up and top‐down approaches show a sink of CO2in natural ecosystems (bottom‐up: −29 (−709, 455), top‐down: −587 (−862, −312) Tg CO2‐C yr−1) and sources of CH4(bottom‐up: 38 (22, 53), top‐down: 15 (11, 18) Tg CH4‐C yr−1) and N2O (bottom‐up: 0.7 (0.1, 1.3), top‐down: 0.09 (−0.19, 0.37) Tg N2O‐N yr−1). The combined global warming potential of all three gases (GWP‐100) cannot be distinguished from neutral. Over shorter timescales (GWP‐20), the region is a net GHG source because CH4dominates the total forcing. The net CO2sink in Boreal forests and wetlands is largely offset by fires and inland water CO2emissions as well as CH4emissions from wetlands and inland waters, with a smaller contribution from N2O emissions. Priorities for future research include the representation of inland waters in process‐based models and the compilation of process‐model ensembles for CH4and N2O. Discrepancies between bottom‐up and top‐down methods call for analyses of how prior flux ensembles impact inversion budgets, more and well‐distributed in situ GHG measurements and improved resolution in upscaling techniques.
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Increased Terrestrial Carbon Export and CO 2 Evasion From Global Inland Waters Since the Preindustrial Era
Abstract Global carbon dioxide (CO2) evasion from inland waters (rivers, lakes, and reservoirs) and carbon (C) export from land to oceans constitute critical terms in the global C budget. However, the magnitudes, spatiotemporal patterns, and underlying mechanisms of these fluxes are poorly constrained. Here, we used a coupled terrestrial–aquatic model to assess how multiple changes in climate, land use, atmospheric CO2concentration, nitrogen (N) deposition, N fertilizer and manure applications have affected global CO2evasion and riverine C export along the terrestrial‐aquatic continuum. We estimate that terrestrial C loadings, riverine C export, and CO2evasion in the preindustrial period (1800s) were 1,820 ± 507 (mean ± standard deviation), 765 ± 132, and 841 ± 190 Tg C yr−1, respectively. During 1800–2019, multifactorial global changes caused an increase of 25% (461 Tg C yr−1) in terrestrial C loadings, reaching 2,281 Tg C yr−1in the 2010s, with 23% (104 Tg C yr−1) of this increase exported to the ocean and 59% (273 Tg C yr−1) being emitted to the atmosphere. Our results showed that global inland water recycles and exports nearly half of the net land C sink into the atmosphere and oceans, highlighting the important role of inland waters in the global C balance, an amount that should be taken into account in future C budgets. Our analysis supports the view that a major feature of the global C cycle–the transfer from land to ocean–has undergone a dramatic change over the last two centuries as a result of human activities.
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- Award ID(s):
- 1903722
- PAR ID:
- 10471144
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Global Biogeochemical Cycles
- Volume:
- 37
- Issue:
- 10
- ISSN:
- 0886-6236
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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