CO-DIAGENESIS OF IRON AND PHOSPHORUS IN HYDROTHERMAL SEDIMENTS FROM THE SOUTHERN EAST PACIFIC RISE: IMPLICATIONS FOR THE EVALUATION OF PALEOSEAWATER PHOSPHATE CONCENTRATIONS

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dc.contributor.author Poulton S.W.
dc.contributor.author Canfield D.E.
dc.date.accessioned 2024-08-09T04:00:34Z
dc.date.available 2024-08-09T04:00:34Z
dc.date.issued 2006
dc.identifier https://elibrary.ru/item.asp?id=12091587
dc.identifier.citation Geochimica et Cosmochimica Acta, 2006, 70, 23 SPEC. ISS., 5883-5898
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/44637
dc.description.abstract We present a detailed study of the co-diagenesis of Fe and P in hydrothermal plume fallout sediments from ?19?S on the southern East Pacific Rise. Three distal sediment cores from 340-1130 km from the ridge crest, collected during DSDP Leg 92, were analysed for solid phase Fe and P associations using sequential chemical extraction techniques. The sediments at all sites are enriched in hydrothermal Fe (oxyhydr)oxides, but during diagenesis a large proportion of the primary ferrihydrite precipitates are transformed to the more stable mineral form of goethite and to a lesser extent to clay minerals, resulting in the release to solution of scavenged P. However, a significant proportion of this P is retained within the sediment, by incorporation into secondary goethite, by precipitation as authigenic apatite, and by readsorption to Fe (oxyhydr)oxides. Molar P/Fe ratios for these sediments are significantly lower than those measured in plume particles from more northern localities along the southern East Pacific Rise, and show a distinct downcore decrease to a depth of ?12 m. Molar P/Fe ratios are then relatively constant to a depth of ?35 m. The Fe and P speciation data indicate that diagenetic modification of the sediments is largely complete by a depth of 2.5 m, and thus depth trends in molar P/Fe ratios can not solely be explained by losses of P from the sediment by diffusion to the overlying water column during early diagenesis. Instead, these sediments are likely recording changes in dissolved P concentrations off the SEPR, possibly as a result of redistribution of nutrients in response to changes in oceanic circulation over the last 10 million years. Furthermore, the relatively low molar P/Fe ratios observed throughout these sediments are not necessarily solely due to losses of scavenged P by diffusion to the overlying water column during diagenesis, but may also reflect post-depositional oxidation of pyrite originating from the volatile-rich vents of the southern East Pacific Rise. This study suggests that the molar P/Fe ratio of oxic Fe-rich sediments may serve as a proxy of relative changes in paleoseawater phosphate concentrations, particularly if Fe sulfide minerals are not an important component during transport and deposition. ? 2006 Elsevier Inc. All rights reserved.
dc.subject APATITE
dc.subject AUTHIGENIC MINERAL
dc.subject CORE ANALYSIS
dc.subject DIAGENESIS
dc.subject DIFFUSION
dc.subject GOETHITE
dc.subject HYDROTHERMAL PLUME
dc.subject IRON
dc.subject PHOSPHORUS
dc.subject SEDIMENT CHEMISTRY
dc.subject EAST PACIFIC RISE
dc.subject PACIFIC OCEAN
dc.title CO-DIAGENESIS OF IRON AND PHOSPHORUS IN HYDROTHERMAL SEDIMENTS FROM THE SOUTHERN EAST PACIFIC RISE: IMPLICATIONS FOR THE EVALUATION OF PALEOSEAWATER PHOSPHATE CONCENTRATIONS
dc.type Статья
dc.identifier.doi 10.1016/j.gca.2006.01.030


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