Dissolved iron (dFe) is an essential micronutrient for phytoplankton, with vanishingly low oceanic dissolved concentrations (pico- to nanomoles per kg) known to limit growth—and thus influence primary productivity and carbon cycling—over much of the surface ocean. However, because of the considerable challenges associated with contamination-free sample collection and accurate analysis of such low dFe concentrations, the first reliable dFe measurements came only in the 1980s. Further, by 2003, despite several decades of research, there were only ~25 full-depth oceanic dFe profiles worldwide, with dust considered to be the main oceanic dFe source. Since 2008, facilitated by the extensive field campaign and rigorous intercalibration of the international GEOTRACES program, there has been an “explosion” in the availability of oceanic dFe data, with hundreds of profiles now available. Concurrently, there has been a paradigm shift to a view of the marine Fe cycle where multiple sources contribute, and some forms of dFe can be transported great distances through the intermediate and deep ocean. Here, we showcase the GEOTRACES dFe datasets across the different ocean basins, synthesize our current multi-source view of the oceanic Fe cycle, spotlight sediments as an important dFe source, and look to future directions for constraining oceanic dFe boundary exchange.
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Probing the bioavailability of dissolved iron to marine eukaryotic phytoplankton using in situ single cell iron quotas
We present a new approach for quantifying the bioavailability of dissolved iron (dFe) to oceanic phytoplankton. Bioavailability is defined using an uptake rate constant (kin-app) computed by combining data on: i) Fe content of individual in situ phytoplankton cells; ii) concurrently-determined seawater dFe concentrations; and iii) growth rates estimated from the PISCES model. We examined 930 phytoplankton cells, collected between 2002-2016 from 45 surface stations during 11 research cruises. This approach is only valid for cells that have upregulated their high-affinity Fe uptake system, so data was screened, yielding 560 single cell kin-app values from 31 low-Fe stations. We normalized kin-app to cell surface area (S.A.) to account for cell-size differences. The resulting bioavailability proxy (kin-app/S.A.) varies among cells, but all values are within bioavailability limits predicted from defined Fe complexes. In situ dFe bioavailability is higher than model Fe-siderophore complexes and often approaches that of highly-available inorganic Fe´. Station averaged kin-app/S.A. are also variable but show no systematic changes across location, temperature, dFe, and phytoplankton taxa. Given the relative consistency of kin-app/S.A. among stations (ca. 5-fold variation), we computed a grand-averaged dFe availability, which upon normalization to cell carbon (C) yields kin-app/C of 42,200 ± 11,000 L mol C-1 d-1. We utilize kin-app/C to calculate dFe uptake rates and residence times in low Fe oceanic regions. Finally, we demonstrate the applicability of kin-app/C for constraining Fe uptake rates in earth system models, such as those predicting climate mediated changes in net primary production in the Fe-limited Equatorial Pacific.
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- PAR ID:
- 10285435
- Date Published:
- Journal Name:
- Global Biogeochemical Cycles
- ISSN:
- 0886-6236
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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