Chasing iron bioavailability in the Southern Ocean: Insights from Phaeocystis antarctica and iron speciation

Author:

Fourquez Marion12ORCID,Janssen David J.3ORCID,Conway Tim M.4ORCID,Cabanes Damien2,Ellwood Michael J.56,Sieber Matthias47ORCID,Trimborn Scarlett8,Hassler Christel2910ORCID

Affiliation:

1. Aix Marseille Univ., Université de Toulon, CNRS, IRD, MIO UMR 110, Marseille 13288, France.

2. University of Geneva, Department F.-A. Forel for Environmental and Aquatic Sciences, Geneva 1211, Switzerland.

3. Department Surface Waters, Eawag–Swiss Federal Institute of Aquatic Science and Technology, Kastanienbaum, Switzerland.

4. College of Marine Science, University of South Florida, St. Petersburg, FL 33701, USA.

5. Research School of Earth Sciences, Australian National University, Canberra, ACT, Australia.

6. Australian Centre for Excellence in Antarctic Science, Research School of Earth Sciences, Australian National University, Canberra, ACT, Australia.

7. Institute of Geochemistry and Petrology, ETH Zürich, Zürich, Switzerland.

8. Alfred Wegener Institute, Helmholtz Center for Polar and Marine Research, Bremerhaven 27570, Germany.

9. Institute of Earth Sciences, University of Lausanne, Lausanne 1015, Switzerland.

10. School of Architecture, Civil, and Environmental Engineering, Ecole Polytechnique Fédérale de Lausanne, Sion 1951, Switzerland.

Abstract

Dissolved iron (dFe) availability limits the uptake of atmospheric CO 2 by the Southern Ocean (SO) biological pump. Hence, any change in bioavailable dFe in this region can directly influence climate. On the basis of Fe uptake experiments with Phaeocystis antarctica , we show that the range of dFe bioavailability in natural samples is wider (<1 to ~200% compared to free inorganic Fe′) than previously thought, with higher bioavailability found near glacial sources. The degree of bioavailability varied regardless of in situ dFe concentration and depth, challenging the consensus that sole dFe concentrations can be used to predict Fe uptake in modeling studies. Further, our data suggest a disproportionately major role of biologically mediated ligands and encourage revisiting the role of humic substances in influencing marine Fe biogeochemical cycling in the SO. Last, we describe a linkage between in situ dFe bioavailability and isotopic signatures that, we anticipate, will stimulate future research.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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