Iron and phosphorus speciations in DSDP Leg 92 sediments


Autoria(s): Poulton, Simon W; Canfield, Donald E
Cobertura

MEDIAN LATITUDE: -19.128400 * MEDIAN LONGITUDE: -120.465867 * SOUTH-BOUND LATITUDE: -19.451500 * WEST-BOUND LONGITUDE: -124.676800 * NORTH-BOUND LATITUDE: -18.929000 * EAST-BOUND LONGITUDE: -116.839500 * DATE/TIME START: 1983-03-17T00:00:00 * DATE/TIME END: 1983-03-23T00:00:00

Data(s)

24/12/2006

Resumo

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.

Formato

application/zip, 6 datasets

Identificador

https://doi.pangaea.de/10.1594/PANGAEA.710890

doi:10.1594/PANGAEA.710890

Idioma(s)

en

Publicador

PANGAEA

Direitos

CC-BY: Creative Commons Attribution 3.0 Unported

Access constraints: unrestricted

Fonte

Supplement to: Poulton, Simon W; Canfield, Donald E (2006): Co-diagenesis of iron and phosphorus in hydrothermal sediments from the southern East Pacific Rise; implications for the evaluation of paleo-sea water phosphate concentrations. Geochimica et Cosmochimica Acta, 70(23), 5883-5898, doi:10.1016/j.gca.2006.01.030

Palavras-Chave #92-598; 92-599; 92-600; Age model; Atomic absorption spectrometry (AAS); biogenic P; extractant: 2 M NH4Cl (pH 7): 8 x 4 h; bound with goethite + hematite; extractant: 0.35 M acetic acid/0.2 M Na-citrate/0.28 M Na dithionite: 2 h; bound with hydrous ferric oxides + lepidocrocite; extractant: 1 M hydroxylamine-HCl in 25% acetic acid (pH 2): 48 h; 1 M MgCl2 (pH 8): 2 x 2 h; CaCO3; Calcium carbonate; Carbon, organic, total; Deep Sea Drilling Project; Depth; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP; Fe; Glomar Challenger; in authigenic apatite + biogenic apatite + CaCO3-bound P; extractant: 1 M Na- acetate (pH 4-acetic acid buffered): 6 h 1 M MgCl2 (pH 8): 2 x 2 h; water wash: 2 h; in detrital apatite + other inorganic P phases; extractant: 1 M HCl: 16 h; in goethite + hematite; extractant: 0.35 M acetic acid/0.2 M Na-citrate/0.28 M Na dithionite: 2 h; in hydrous ferric oxides + lepidocrocite; extractant: 1 M hydroxylamine-HCl in 25% acetic acid (pH 2): 48 h; 1 M MgCl2 (pH 8): 2 x 2 h; in silicates; Iron; iron-bound P; extractant: 0.3 M Na-citrate/1 M NaHCO3/0.14 M Na-dithionite: 8 h 1 M MgCl2 (pH 8): 2 h; water wash: 2 h; Leg92; loosely bound + exchangeable P; extractant: 1 M MgCl2 (pH 8): 2 x 2 h; water wash: 2 x 2 h; organic P; ashing at 550°C: 2 h; extractant: 1 M HCl: 16 h; P; Phosphorus; South Pacific; South Pacific/PLATEAU; TOC; total; UV/VIS Spectrometer; X-ray fluorescence (XRF)
Tipo

Dataset