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Title: Limited contribution of ancient methane to surface waters of the U.S. Beaufort Sea shelf

Journal Article · · Science Advances
ORCiD logo [1]; ORCiD logo [2];  [3];  [2]; ORCiD logo [4]; ORCiD logo [5];  [6];  [7];  [3]
  1. Univ. of Rochester, NY (United States). Dept. of Earth and Environmental Sciences; Stockholm Univ. (Sweden). Dept. of Environmental Science and Analytical Chemistry. Bolin Centre for Climate Research
  2. Univ. of Rochester, NY (United States). Dept. of Earth and Environmental Sciences
  3. Univ. of California, Irvine, CA (United States). Keck Carbon Cycle Accelerator Mass Spectrometry Lab. Dept. of Earth System Science
  4. Univ. of Minnesota, Duluth, MN (United States). Large Lakes Observatory. Dept. of Chemistry and Biochemistry
  5. U.S. Geological Survey, Woods Hole, MA (United States)
  6. Univ. of Colorado, Boulder, CO (United States). Cooperative Inst. for Research in Environmental Sciences; National Oceanic and Atmospheric Administration (NOAA), Boulder, CO (United States). Global Monitoring Division. Earth System Research Lab.
  7. Univ. of Colorado, Boulder, CO (United States). Inst. of Arctic and Alpine Research

In response to warming climate, methane can be released to Arctic Ocean sediment and waters from thawing subsea permafrost and decomposing methane hydrates. However, it is unknown whether methane derived from this sediment storehouse of frozen ancient carbon reaches the atmosphere. We quantified the fraction of methane derived from ancient sources in shelf waters of the U.S. Beaufort Sea, a region that has both permafrost and methane hydrates and is experiencing significant warming. Although the radiocarbon-methane analyses indicate that ancient carbon is being mobilized and emitted as methane into shelf bottom waters, surprisingly, we find that methane in surface waters is principally derived from modern-aged carbon. We report that at and beyond approximately the 30-m isobath, ancient sources that dominate in deep waters contribute, at most, 10 ± 3% of the surface water methane. These results suggest that even if there is a heightened liberation of ancient carbon–sourced methane as climate change proceeds, oceanic oxidation and dispersion processes can strongly limit its emission to the atmosphere.

Research Organization:
Univ. of Rochester, NY (United States)
Sponsoring Organization:
USDOE Office of Fossil Energy (FE); National Science Foundation (NSF)
Grant/Contract Number:
FE0028980; PLR-1417149
OSTI ID:
1499955
Journal Information:
Science Advances, Vol. 4, Issue 1; ISSN 2375-2548
Publisher:
AAASCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 34 works
Citation information provided by
Web of Science

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Cited By (10)

Methane Feedbacks to the Global Climate System in a Warmer World journal March 2018
Radiocarbon Analysis of Methane at the NERC Radiocarbon Facility (East Kilbride) journal April 2019
Methane Sources in the Waters of Lake Michigan and Lake Superior as Revealed by Natural Radiocarbon Measurements journal May 2019
Preindustrial 14CH4 indicates greater anthropogenic fossil CH4 emissions journal February 2020
Interpreting contemporary trends in atmospheric methane journal February 2019
Shipborne eddy covariance observations of methane fluxes constrain Arctic sea emissions journal January 2020
Comment on “The origin of methane in the East Siberian Arctic Shelf unraveled with triple isotope analysis” by Sapart et al. (2017) journal January 2018
Preindustrial 14CH4 indicates greater anthropogenic fossil CH4 emissions text January 2020
Carbon isotopes (13C and 14C) and concentrations of dissolved methane (CH4) in surface waters sampled in June 2019 at the Coal Oil Point seep field of the Santa Barbara Basin dataset January 2020
Radiocarbon in methane from waters of the US Atlantic and Pacific margins as collected on R/V Hugh Sharp cruise HRS1713 and R/V Rachel Carson cruise RC0026 in 2017 and 2019 dataset January 2021

Figures / Tables (3)


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