The Distinct Composition and Transformation of Terrestrial Organic Carbon in the Yukon River Delta and Plume During the Mighty Spring Freshet

Author:

Burns A. J.1ORCID,Spencer R. G. M.2ORCID,Kellerman A. M.2ORCID,Yan G.3,Leonard L.3,Kaiser K.3ORCID,Mannino A.4ORCID,Tzortziou M.5ORCID,Hernes P. J.1ORCID

Affiliation:

1. Department of Land, Air and Water Resources University of California, Davis Davis CA USA

2. National High Magnetic Field Laboratory Geochemistry Group Department of Earth, Ocean, and Atmospheric Science Florida State University Tallahassee FL USA

3. Department of Marine and Coastal Environmental Science Texas A&M University Galveston TX USA

4. Ocean Ecology Laboratory (Code 616) NASA Goddard Space Flight Center Greenbelt MD USA

5. Earth and Atmospheric Sciences Department The City College of New York New York NY USA

Abstract

AbstractArctic amplification is leading to increased terrestrial organic carbon (terrOC) mobilization with downstream impacts on riverine and marine biogeochemistry. To improve quantification and characterization of terrOC discharged to the Arctic Ocean, Yukon River delta samples were collected during three stages of the annual hydrograph (ascending limb/peak freshet, descending limb, late summer) and across a land‐to‐ocean salinity gradient (0.08–29.06 ppt). All samples were analyzed for dissolved organic carbon (DOC) concentration and lignin phenols to determine seasonal variability in riverine terrOC and salinity‐induced transformation of highly aromatic terrestrial compounds. Additionally, the relationship between lignin and absorbance at 350 and 412 nm was assessed to determine the feasibility of using optical proxies for accurate quantification, both seasonally and across expansive salinity gradients. Lignin phenols were highest during the ascending limb/peak freshet (0.58–0.97 mg/100 mg OC) when riverine DOC was dominated by young vascular plant sources, whereas lignin phenols were lower (0.15–0.89 mg/100 mg OC) and riverine DOC more variable in terrestrial source and diagenetic state during the descending limb and late summer. Across the sampled salinity gradient, there was disproportionate depletion of lignin (up to 73%) compared to DOC (up to 22%). Finally, while optical proxies can be used to quantify lignin within seasonal or spatial contexts, increased uncertainty is likely when expanding linear correlations across Arctic land‐ocean continuums. Overall, results indicate seasonal, spatial, interannual, and climatic controls that are amplified during high‐flow conditions and important to constrain when investigating Arctic terrOC cycling and land‐ocean DOC flux.

Publisher

American Geophysical Union (AGU)

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