Abstract

Abstract Marine sediments contain two isotopically distinct components: a non-desorbable fraction with δ11B between −4.3 and +2.8 per mil (n = 10) and a desorbable component with δ11B between 13.9 and 15.8 per mil (n = 6). The adsorption coefficient, K, for the uptake of B from seawater by fluvial suspended material (Mississippi) has an experimentally determined value of 1.54 ± 0.05. The associated isotope fractionation factor, α, is 0.974 ± 0.003. Empirical values for K, determined from the analysis of marine sediments (n = 6), were between 3 and 4. The amount of B adsorbed onto fluvial suspended material during estuarine mixing is about 9 × 109 moles/yr. Based on pore water data, adsorption experiments and comparative size fraction analyses (suspended sediments from the Mississippi River vs. bottom deposits from the Delta) there is no evidence for the incorporation of B into detrital sediments at low temperature. However, the high B content of Bauer Deep metalliferous sediments must be due to incorporation of seawater B during formation of authigenic silicates. The δ11B of these minerals is 2 ± 3 per mil. Hydrothermally altered sediments from DSDP Hole 477, Guaymas Basin, Gulf of California have variable B contents, from 33 ppm, similar to the unaltered detritus, to 1.2 ppm in the recrystallized material. The latter has δ11B as low as −9.0 per mil, substantially lower than the unaltered material. Hydrothermal solutions collected from vents adjacent to the hole have boron contents elevated by about a factor of 4 relative to seawater and δ11B between 16.5 and 23.2 per mil. The B mobilized from the sediments is isotopically fractionated with the fluids being preferentially enriched in the heavy isotope. Analysis of an oxisol profile developed over granite in the Guyana Shield showed that boron is partially mobilized during weathering with an isotopic offset of 2.5 per mil between bedrock and soil. The observed enrichment of B in shales relative to igneous rocks does not occur during weathering or during exposure to seawater at low temperature. Incorporation occurs only during burial diagenesis at temperatures greater than about 60°C. However, the enrichments cannot be attained during a single cycle of primary weathering and burial but must be cumulative over many cycles.

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