Tracers of chemical scavenging in the ocean: boundary effects and large-scale chemical fractionation
- 25 May 1988
- journal article
- Published by The Royal Society in Philosophical Transactions of the Royal Society of London. Series A, Mathematical and Physical Sciences
- Vol. 325 (1583), 147-160
- https://doi.org/10.1098/rsta.1988.0048
Abstract
Several nuclides in the natural radioactive decay series display a strong non-conservative behaviour in the oceanic water column because of their removal to the sediments by uptake at the solid-solution interface. This removal process is commonly referred to as scavenging, and it is believed to be important in governing the behaviour of many heavy metals and other trace substances in the ocean. Measurements of radioactive disequilibrium in seawater yield estimates of the rate at which scavenging occurs. Results show that removal times by scavenging are comparable to within-basin lateral mixing times. It follows that the distribution of the scavenged tracers should be sensitive to the spatial distribution of their sinks, and this has been demonstrated by observation, most notably in the case of $^{210}$Pb. The distribution of $^{210}$Pb suggests a strong control by intensified uptake at boundaries, especially at the ocean margins. This conclusion has been confirmed by sediment traps and by measurements of $^{210}$Pb accumulations in the sediment column. A similar phenomenon of intensified scavenging at ocean margins has been observed for $^{231}$Pa. Studies with $^{230}$Th, on the other hand, show that its delivery to the sediments is mainly caused by the local flux of sinking particles. Thus two transport pathways for removal by scavenging are envisioned, one with a strong horizontal component due to the intensified uptake at the margins and the other with a strong vertical component due to the particle flux. Important large-scale chemical fractionations, best illustrated by comparative studies of $^{230}$Th and $^{231}$Pa, are produced by differential partitioning of elements between these two pathways. Model calculations suggest that horizontal mixing rate and particle flux are important variables controlling the partitioning of reactive chemical substances between pelagic sediments of the interior ocean and hemipelagic sediments of the ocean margins. Changes in the extent of this partitioning through time may be recorded as changes in the $^{230}$Th/$^{231}$Pa ratio through the sediment column.Keywords
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