Geochemistry of secondary carbonates in ODP Leg 115 basalts


Autoria(s): Burns, Stephen J; Swart, Peter K; Baker, Paul A
Cobertura

MEDIAN LATITUDE: -1.231900 * MEDIAN LONGITUDE: 66.424050 * SOUTH-BOUND LATITUDE: -7.545300 * WEST-BOUND LONGITUDE: 59.016800 * NORTH-BOUND LATITUDE: 5.081500 * EAST-BOUND LONGITUDE: 73.831300 * DATE/TIME START: 1987-05-29T10:30:00 * DATE/TIME END: 1987-06-28T07:45:00

Data(s)

14/01/1990

Resumo

This report presents the results of a study of the stable isotopic and chemical composition of secondary carbonate minerals precipitated within basalts at Ocean Drilling Program Sites 707 and 715. At Site 715, the secondary carbonates are all composed of calcite and display a narrow range of carbon and oxygen stable isotope ratios, with values ranging from -2.75 per mil to 1.95 per mil PDB and -0.27 per mil to 2.86 per mil PDB, respectively. Strontium, iron, and manganese values of the samples are generally low. The geochemistry of Site 715 samples indicates that they precipitated from seawater-domi- nated fluids, at low temperatures, as is typical of secondary carbonates from most Deep Sea Drilling Project sites. In contrast, at Site 707, aragonite, siderite, and manganese-rich calcite occur as secondary carbonates in addition to calcite. The carbon isotopes of the Site 707 carbonates of all rock types are depleted in 13C. Values range from -2.79 per mil to -16.43 per mil PDB. Oxygen isotope values do not show a wide variation, ranging from -1.78 per mil to 1.17 per mil. The strontium contents of the samples range from 5200 to 8100 ppm for aragonites, and from 145 to 862 ppm for calcites. Iron and manganese contents are high in calcites and siderites and low in aragonites. Site 707 carbonates precipitated at low temperatures in a fairly closed system, in which basalt-seawater interaction has greatly influenced the chemistry of the pore fluids. The reactions occurring within the system before and in conjunction with secondary carbonate precipita- tion include oxidation of isotopically light methane, derived from fluids circulating within the basalts, and reduction of substantial amounts of iron and manganese oxides from the basalts.

Formato

application/zip, 2 datasets

Identificador

https://doi.pangaea.de/10.1594/PANGAEA.755765

doi:10.1594/PANGAEA.755765

Idioma(s)

en

Publicador

PANGAEA

Direitos

CC-BY: Creative Commons Attribution 3.0 Unported

Access constraints: unrestricted

Fonte

Supplement to: Burns, Stephen J; Swart, Peter K; Baker, Paul A (1990): Geochemistry of secondary carbonates in Leg 115 basalts: tracers of basalt/seawater interaction. In: Duncan, RA; Backmann, J; Peterson, LC; et al. (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 115, 93-101, doi:10.2973/odp.proc.sr.115.183.1990

Palavras-Chave #115-707C; 115-715A; assuming d18O H2O = -1 per mil SMOW; Atomic absorption spectrometry (AAS), Perkin-Elmer; Calculated (Epstein et al., 1953); d13C; d18O; delta 13C; delta 18O; Depth; DEPTH, sediment/rock; DRILL; Drilling/drill rig; Event; Fe; Iron; Joides Resolution; Label; Lakshadweep Sea; Leg115; Magnesium; Manganese; Mass spectrometer Finnigan MAT 251; Mg; Mn; Ocean Drilling Program; ODP; ODP sample designation; Rock; Rock type; Samp com; Sample code/label; Sample comment; South Indian Ridge, South Indian Ocean; Sr; Strontium; T cal; Temperature, calculated; Type; X-ray diffraction (XRD)
Tipo

Dataset