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  • OceanRep  (3)
  • AGU (American Geophysical Union)  (2)
  • Nature Publishing Group  (1)
  • Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu
Document type
Publisher
  • AGU (American Geophysical Union)  (2)
  • Nature Publishing Group  (1)
  • Biological and Chemical Oceanography Data Management Office (BCO-DMO). Contact: bco-dmo-data@whoi.edu
  • Wiley  (2)
  • Elsevier  (1)
Years
  • 1
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    Nature Publishing Group
    In:  Nature Geoscience, 3 (6). pp. 412-416.
    Publication Date: 2017-12-21
    Description: The elemental stoichiometry of sea water and particulate organic matter is remarkably similar. This observation led Redfield to hypothesize that the oceanic ratio of nitrate to phosphate is controlled by the remineralization of phytoplankton biomass1. The Redfield ratio is used universally to quantitatively link the marine nitrogen and phosphorus cycles in numerous biogeochemical applications2,3,4. Yet, empirical and theoretical studies show that the ratio of nitrogen to phosphorus in phytoplankton varies greatly with taxa5,6 and growth conditions7,8,9. Here we present a dynamic five-box ecosystem model showing that non-Redfield utilization of dissolved nitrogen and phosphorus by non-nitrogen-fixing phytoplankton controls the magnitude and distribution of nitrogen fixation. In our simulations, systems dominated by rapidly growing phytoplankton with low nitrogen to phosphorus uptake ratios reduce the phosphorus available for nitrogen fixation. In contrast, in systems dominated by slow-growing phytoplankton with high nitrogen to phosphorus uptake ratios nitrogen deficits are enhanced, and nitrogen fixation is promoted. We show that estimates of nitrogen fixation are up to fourfold too high when non-Redfield uptake stoichiometries are ignored. We suggest that the relative abundance of fast- and slow-growing phytoplankton controls the amount of new nitrogen added to the ocean.
    Type: Article , PeerReviewed
    Format: text
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  • 2
    Publication Date: 2019-07-08
    Description: Surface delta(15)N(PON) increased 3.92 +/- 0.48 over the course of 20 days following additions of iron (Fe) to an eddy in close proximity to the Antarctic Polar Front in the Atlantic sector of the Southern Ocean. The change in delta(15)N(PON) was associated with an increase in the 〉20 mu m size fraction, leading to a maximal difference of 6.23 between the 〉20 mu m and 〈20 mu m size fractions. Surface delta(13)C(POC) increased 1.18 +/- 0.31 over the same period. After a decrease in particulate organic matter in the surface layer, a second phytoplankton community developed that accumulated less biomass, had a slower growth rate and was characterized by an offset of 1.56 in delta(13)C(POC) relative to the first community. During growth of the second community, surface delta(13)C(POC) further increased 0.83 +/- 0.13. Here we speculate on ways that carboxylation, nitrogen assimilation, substrate pool enrichment and community composition may have contributed to the gradual increase in delta(13)C(POC) associated with phytoplankton biomass accumulation, as well as the systematic offset in delta(13)C(POC) between the two phytoplankton communities.
    Type: Article , PeerReviewed
    Format: text
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  • 3
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    AGU (American Geophysical Union) | Wiley
    In:  Global Biogeochemical Cycles, 27 (1). pp. 11-20.
    Publication Date: 2016-05-02
    Description: We combined data sets of measured sedimentary calcium carbonate (CaCO3) and satellite-derived pelagic primary production to parameterize the relation between CaCO3 content on the Antarctic shelves and primary production in the overlying water column. CaCO3 content predicted in this way was in good agreement with the measured data. The parameterization was then used to chart CaCO3 content on the Antarctic shelves all around the Antarctic, using the satellite-derived primary production. The total inventory of CaCO3 in the bioturbated layer of Antarctic shelf sediments was estimated to be 0.5 Pg C. This quantity is comparable to the total CO2 uptake by the Southern Ocean in only one to a few years (dependent on the uptake estimate and area considered), indicating that the dissolution of these carbonates will neither delay ocean acidification in this area nor augment the Southern Ocean CO2 uptake capacity.
    Type: Article , PeerReviewed
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