Iron isotope insights into equatorial Pacific biogeochemistry

Abstract

The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8500 km along the equator and in the upper 1000 m of the water column.δ56DFe and δ56PFe ranged from -0.22 ‰ to +0.79 ± 0.07 ‰ and from -0.52 ‰ to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated an equilibrium fractionation and the co-occurrence of chemical fluxes from both phases toward the other. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014) and extends up to 1200 km from the coast. In the open ocean area, preservation of a DFe isotopic signature of ∼ +0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7800 km), confirmed the origin of the DFe carried within this current toward the HNLC region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that iron was originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that any fractionation, if present, must be small, no larger than a few tenths of a per mil.