The stable isotope composition of radiogenic and natural elements provides a powerful tool for unraveling element sources and biogeochemical processes in the marine environment. Depending on the element, trace element isotope ratios can (1) narrow possible sources of the element in a sample and/or (given a temporal history boundary condition) constrain the time the when the element departed the ocean surface (e.g., Pb, Nd), (2) provide information on redox processes that the element is directly or indirectly involved in (e.g., Fe, Mo, Tl), (3) indicate the extent of biological uptake and/or ocean mixing of the element (e.g., Cd, Zn).However, these trace metals occur at picomolar to nanomolar concentrations, and precise stable isotope measurements require 100-1000 times more sample than required for concentration determination.
AbstractWe report data on the isotopic composition of cadmium, copper, iron, lead, zinc, and molybdenum at the GEOTRACES IC1 BATS Atlantic intercalibration station. In general, the between lab and within-lab precisions are adequate to resolve global gradients and vertical gradients at this station for Cd, Fe, Pb, and Zn. Cd and Zn isotopes show clear variations in the upper water column and more subtle variations in the deep water; these variations are attributable, in part, to progressive mass fractionation of isotopes by Rayleigh distillation from biogenic uptake and/or adsorption. Fe isotope variability is attributed to heavier crustal dust and hydrothermal sources and light Fe from reducing sediments. Pb isotope variability results from temporal changes in anthropogenic source isotopic compositions and the relative contributions of U.S. and European Pb sources. Cu and Mo isotope variability is more subtle and close to analytical precision. Although the present situation is adequate for proceeding with GEOTRACES, it should be possible to improve the within-lab and between-lab precisions for some of these properties.