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  • Primary Production  (1)
  • SO4 addition  (1)
  • Stream  (1)
  • Springer  (3)
  • 1
    Publication Date: 2022-05-25
    Description: © The Author(s), 2011. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Estuaries and Coasts 35 (2012): 401-415, doi:10.1007/s12237-011-9417-3.
    Description: Although the Arctic Ocean is the most riverine-influenced of all of the world’s oceans, the importance of terrigenous nutrients in this environment is poorly understood. This study couples estimates of circumpolar riverine nutrient fluxes from the PARTNERS (Pan-Arctic River Transport of Nutrients, Organic Matter, and Suspended Sediments) Project with a regionally configured version of the MIT general circulation model to develop estimates of the distribution and availability of dissolved riverine N in the Arctic Ocean, assess its importance for primary production, and compare these estimates to potential bacterial production fueled by riverine C. Because riverine dissolved organic nitrogen is remineralized slowly, riverine N is available for uptake well into the open ocean. Despite this, we estimate that even when recycling is considered, riverine N may support 0.5–1.5 Tmol C year−1 of primary production, a small proportion of total Arctic Ocean photosynthesis. Rapid uptake of dissolved inorganic nitrogen coupled with relatively high rates of dissolved organic nitrogen regeneration in N-limited nearshore regions, however, leads to potential localized rates of riverine-supported photosynthesis that represent a substantial proportion of nearshore production.
    Description: Funding for this work was provided through NSFOPP- 0229302 and NSF-OPP-0732985.Support to SET was additionally provided by an NSERC Postdoctoral Fellowship.
    Keywords: Arctic Ocean ; Primary Production ; Land–ocean coupling ; Estuarine processes ; Riverine nutrients ; Dissolved organic matter ; Photodegradation
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 2
    Publication Date: 2022-05-26
    Description: © The Authors, 2010. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License. The definitive version was published in Biogeochemistry 103 (2011): 109-124, doi:10.1007/s10533-010-9451-4.
    Description: As the planet warms, widespread changes in Arctic hydrology and biogeochemistry have been documented and these changes are expected to accelerate in the future. Improved understanding of the behavior of water-borne constituents in Arctic rivers with varying hydrologic conditions, including seasonal variations in discharge–concentration relationships, will improve our ability to anticipate future changes in biogeochemical budgets due to changing hydrology. We studied the relationship between seasonal water discharge and dissolved organic carbon and nitrogen (DOC and DON) and nutrient concentrations in the upper Kuparuk River, Arctic Alaska. Fluxes of most constituents were highest during initial snowmelt runoff in spring, indicating that this historically under-studied period contributes significantly to total annual export. In particular, the initial snowmelt period (the stream is completely frozen during the winter) accounted for upwards of 35% of total export of DOC and DON estimated for the entire study period. DOC and DON concentrations were positively correlated with discharge whereas nitrate (NO3 −) and silicate were negatively correlated with discharge throughout the study. However, discharge-specific DOC and DON concentrations (i.e. concentrations compared at the same discharge level) decreased over the summer whereas discharge-specific concentrations of NO3 − and silicate increased. Soluble reactive phosphorus (SRP) and ammonium (NH4 +) were negatively correlated with discharge during the spring thaw, but were less predictable with respect to discharge thereafter. These data provide valuable information on how Arctic watershed biogeochemistry will be affected by future changes in temperature, snowfall, and rainfall in the Arctic. In particular, our results add to a growing body of research showing that nutrient export per unit of stream discharge, particularly NO3 −, is increasing in the Arctic.
    Description: Funding provided by the National Science Foundation, NSF-OPP- 0436118.
    Keywords: Arctic ; Stream ; Headwaters ; Carbon ; Nitrogen ; Nutrients
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 3
    ISSN: 1573-515X
    Keywords: 34S ; sulfate reduction ; sulfide oxidation ; SO4 addition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract We investigated the effects of sulfate concentration on sulfate reduction and net S storage in lake sediments using34S as a tracer. The water overlying intact sediment cores from the hypolimnion of Mares Pond, MA, was replaced with two Na2 34SO4 solutions at either ambient (70 μM) or elevated (260 μM) sulfate concentrations. The δ34S of the added sulfate was 4974 ‰. Over two months, the net sulfate reduction rate in the ambient sulfate treatment was zero, while the net rate for the high sulfate treatment was 140 μmoles/m2/d. The water overlying the cores was kept under oxic conditions and the sediment received no fresh carbon inputs, thus the net rate reported may underestimate the in situ rate. Gross sulfate reduction rates calculated by isotope dilution were approximately 350 μmoles/m2/d for both treatments. While the calculation of gross sulfate reduction rates in intact sediment cores can be complicated by differential diffusion of34S and32S, isotopic fractionation, and the possible formation of ester sulfates, we believe these effects to be small. The results suggest that sulfate reduction is not strongly sulfate-limited in Mares Pond. The difference in net sulfate reduction rates between treatments resulted from a decrease in sulfide oxidation and suggests the importance of reoxidation in controlling net S storage in lake sediments. In both treatments the CRS and organic S fractions were measurably labelled in34S. Below the sediment surface, the CRS fraction was the more heavily labelled storage product for reduced sulfides.
    Type of Medium: Electronic Resource
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