A land-to-ocean perspective on the magnitude, source and implication of DIC flux from major Arctic rivers to the Arctic Ocean

dc.contributor.author Tank, Suzanne E.
dc.contributor.author Raymond, Peter A.
dc.contributor.author Striegl, Robert G.
dc.contributor.author McClelland, James W.
dc.contributor.author Holmes, Robert M.
dc.contributor.author Fiske, Gregory J.
dc.contributor.author Peterson, Bruce J.
dc.date.accessioned 2013-01-15T20:57:36Z
dc.date.available 2014-10-22T08:57:23Z
dc.date.issued 2012-12-14
dc.description Author Posting. © American Geophysical Union, 2012. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Biogeochemical Cycles 26 (2012): GB4018, doi:10.1029/2011GB004192. en_US
dc.description.abstract A series of seasonally distributed measurements from the six largest Arctic rivers (the Ob', Yenisey, Lena, Kolyma, Yukon and Mackenzie) was used to examine the magnitude and significance of Arctic riverine DIC flux to larger scale C dynamics within the Arctic system. DIC concentration showed considerable, and synchronous, seasonal variation across these six large Arctic rivers, which have an estimated combined annual DIC flux of 30 Tg C yr−1. By examining the relationship between DIC flux and landscape variables known to regulate riverine DIC, we extrapolate to a DIC flux of 57 ± 9.9 Tg C yr−1for the full pan-arctic basin, and show that DIC export increases with runoff, the extent of carbonate rocks and glacial coverage, but decreases with permafrost extent. This pan-arctic riverine DIC estimate represents 13–15% of the total global DIC flux. The annual flux of selected ions (HCO3−, Na+, Ca2+, Mg2+, Sr2+, and Cl−) from the six largest Arctic rivers confirms that chemical weathering is dominated by inputs from carbonate rocks in the North American watersheds, but points to a more important role for silicate rocks in Siberian watersheds. In the coastal ocean, river water-induced decreases in aragonite saturation (i.e., an ocean acidification effect) appears to be much more pronounced in Siberia than in the North American Arctic, and stronger in the winter and spring than in the late summer. Accounting for seasonal variation in the flux of DIC and other major ions gives a much clearer understanding of the importance of riverine DIC within the broader pan-arctic C cycle. en_US
dc.description.embargo 2013-06-14 en_US
dc.description.sponsorship Funding for this work was provided through NSF-OPP-0229302 and NSF-OPP-0732985. Additional support to SET was provided by an NSERC Postdoctoral Fellowship. en_US
dc.format.mimetype application/pdf
dc.identifier.citation Global Biogeochemical Cycles 26 (2012): GB4018 en_US
dc.identifier.doi 10.1029/2011GB004192
dc.identifier.uri https://hdl.handle.net/1912/5718
dc.language.iso en_US en_US
dc.publisher American Geophysical Union en_US
dc.relation.uri https://doi.org/10.1029/2011GB004192
dc.subject Arctic en_US
dc.subject Dissolved inorganic carbon en_US
dc.subject Ocean acidification en_US
dc.subject Permafrost en_US
dc.subject River biogeochemistry en_US
dc.subject Weathering en_US
dc.title A land-to-ocean perspective on the magnitude, source and implication of DIC flux from major Arctic rivers to the Arctic Ocean en_US
dc.type Article en_US
dspace.entity.type Publication
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