Depth distribution of Zr and Nb in seawater: The potential role of colloids or organic complexation to explain non-scavenging-type behavior

Dissolved zirconium (Zr) and niobium (Nb) are present in open-ocean seawater in low pmol/kg concentrations and studies for the Pacific Ocean reported an increase in concentration with depth although both metals are characterized as being particle-reactive. We analyzed dissolved Zr and Nb in 194 Atla...

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Bibliographic Details
Published inMarine chemistry Vol. 188; pp. 18 - 32
Main Authors Poehle, Sandra, Koschinsky, Andrea
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.01.2017
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Summary:Dissolved zirconium (Zr) and niobium (Nb) are present in open-ocean seawater in low pmol/kg concentrations and studies for the Pacific Ocean reported an increase in concentration with depth although both metals are characterized as being particle-reactive. We analyzed dissolved Zr and Nb in 194 Atlantic seawater samples (0.2μm filtered) collected at 16 stations located in the (sub)tropical Atlantic during GEOTRACES cruise M81/1 (GA11) and 6 Pacific samples (0.2μm and 0.015μm filtered) collected from a hydrothermal plume and the background seawater during SO229. Measurements were done using our newly developed online-preconcentration method for the SeaFAST-system with subsequent analysis by inductively coupled plasma-mass spectrometry. Our results showed an increase in dissolved Zr with depth with some distinct maxima at intermediate depths along a NE-SW transect (30°N to 12°S) in the Atlantic. Surface depletion was less pronounced along the Atlantic SE-NW transect (12°S to 8°N) and disappeared almost completely at the northernmost station at 8°N. Dissolved Nb was almost conservatively distributed except off West Africa where a surface depletion was observed. We suggest that dust deposited off West Africa scavenged Zr and Nb from surface waters and riverine discharge from the Amazon may represent a source to the West Atlantic. The correlation of Zr with Si hints to a coupling of Zr to the uptake and release on and from Si particles such as biogenic opal. Analysis of the size-fractionated Pacific samples ruled out a significant colloidal (0.015μm–0.2μm) component as host for Zr and Nb. We suggest that dissolved Zr and Nb might be stabilized by organic complexation in deep waters because both elements form very stable complexes with organic molecules such as siderophores. •Dissolved Zr and Nb increase with increasing water depth in (sub)tropical Atlantic•Sorption of Zr and Nb onto deposited minerals in surface waters off West Africa•Correlation between dissolved Zr and Si except in surface waters•Potential stabilization of Zr and Nb in deep waters through organic complexation•Dissolved Zr and Nb in deep Pacific waters present in <0.015μm fraction
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ISSN:0304-4203
1872-7581
DOI:10.1016/j.marchem.2016.12.001