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Sources and sinks of methane in sea ice: insights from stable isotopes
Jacques, C.; Sapart, C.J.; Fripiat, F.; Carnat, G.; Zhou, J.; Delille, B.; Röckmann, T.; van der Veen, C.; Niemann, H.; Haskell, T.; Tison, J.-L. (2021). Sources and sinks of methane in sea ice: insights from stable isotopes. Elem. Sci. Anth. 9(1): 00167. https://dx.doi.org/10.1525/elementa.2020.00167
In: Elementa Science of the Anthropocene. BioOne: Washington. e-ISSN 2325-1026, meer
Peer reviewed article  

Beschikbaar in  Auteurs 

Trefwoord
    Marien/Kust
Author keywords
    Antarctic; Arctic; Consumption pathways; Methane; Production; Sea ice; Stable isotopes

Auteurs  Top 
  • Zhou, J., meer
  • Delille, B., meer
  • Röckmann, T.
  • van der Veen, C.

Abstract

    We report on methane (CH4) stable isotope (d13C and d 2H) measurements from landfast sea ice collected near Barrow (Utqiagvik, Alaska) and Cape Evans (Antarctica) over the winter-to-springtransition. These measurements provide novel insights into pathways of CH 4 production and consumption in sea ice. We found substantial differences between the two sites. Sea ice overlying the shallow shelf of Barrow was supersaturated in CH4 with a clear microbial origin, most likely from methanogenesis in the sediments. We estimated that in situCH4 oxidation consumed a substantial fraction of the CH 4 being supplied to the sea ice, partly explaining the large range of isotopic values observed (d13C between -68.5 and -48.5 ‰ and d2H between -246 and -104 ‰). Sea ice at Cape Evans wasalso supersaturated in CH4 but with surprisingly high d 13C values (between -46.9 and -13.0 ‰), whereas d2H values (between -313 and -113 ‰) were in the range of those observed at Barrow.These are the first measurements of CH4 isotopic composition in Antarctic sea ice. Our data set suggests a potential combination of a hydrothermal source, in the vicinity of the Mount Erebus, with aerobic CH4 formation in sea ice, although the metabolic pathway for the latter still needs to be elucidated. Our observations show that sea ice needs to be considered as an active biogeochemical interface, contributing to CH4 production and consumption, which disputes the standing paradigm that sea ice is an inert barrier passively accumulating CH4 at the ocean-atmosphere boundary.


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