Document Type
Article
Department or Administrative Unit
Chemistry
Publication Date
10-10-2014
Abstract
This work presents iron isotope data in the western equatorial Pacific. Marine aerosols and top core margin sediments display a slightly heavy Fe isotopic composition (δ56Fe) of 0.33 ± 0.11‰ (2SD) and 0.14 ± 0.07‰, respectively. Samples reflecting the influence of Papua New Guinea runoff (Sepik River and Rabaul volcano water) are characterized by crustal values. In seawater, Fe is mainly supplied in the particulate form and is found with a δ56Fe between −0.49 and 0.34 ± 0.07‰. The particulate Fe seems to be brought mainly by runoff and transported across continental shelves and slopes. Aerosols are suspected to enrich the surface Vitiaz Strait waters, while hydrothermal activity likely enriched New Ireland waters. Dissolved Fe isotopic ratios are found between −0.03 and 0.53 ± 0.07‰. They are almost systematically heavier than the corresponding particulate Fe, and the difference between the signature of both phases is similar for most samples with Δ56FeDFe – PFe = +0.27 ± 0.25‰ (2SD). This is interpreted as an equilibrium isotopic fractionation revealing exchange fluxes between both phases. The dissolved phase being heavier than the particles suggests that the exchanges result in a net nonreductive release of dissolved Fe. This process seems to be locally significantly more intense than Fe reductive dissolution documented along reducing margins. It may therefore constitute a very significant iron source to the ocean, thereby influencing the actual estimation of the iron residence time and sinks. The underlying processes could also apply to other elements.
Recommended Citation
Labatut, M., F. Lacan, C. Pradoux, J. Chmeleff, A. Radic, J. W. Murray, F. Poitrasson, A. M. Johansen, and F. Thil (2014), Iron sources and dissolved particulate interactions in the seawater of the Western Equatorial Pacific, iron isotope perspectives, Global Biogeochem. Cycles, 28, 1044–1065, doi:10.1002/2014GB004928.
Journal
Global Biogeochemical Cycles
Rights
© 2014. American Geophysical Union. All Rights Reserved.
Included in
Environmental Chemistry Commons, Environmental Sciences Commons, Geochemistry Commons, Marine Biology Commons, Oceanography Commons
Comments
This article was originally published in Global Biogeochemical Cycles. The full-text article from the publisher can be found here.