Mineral, chemical and isotopic compositions of altered rocks at ODP Sites 193-1188 and 193-1189


Autoria(s): Lackschewitz, Klas S; Devey, Colin W; Stoffers, Peter; Botz, Reiner; Eisenhauer, Anton; Kummetz, M; Schmidt, Mark; Singer, A
Cobertura

MEDIAN LATITUDE: -3.725683 * MEDIAN LONGITUDE: 151.671567 * SOUTH-BOUND LATITUDE: -3.728300 * WEST-BOUND LONGITUDE: 151.669800 * NORTH-BOUND LATITUDE: -3.720600 * EAST-BOUND LONGITUDE: 151.675100 * DATE/TIME START: 2000-11-18T17:30:00 * DATE/TIME END: 2000-12-30T04:00:00

Data(s)

16/12/2004

Resumo

During ODP Leg 193, 4 sites were drilled in the active PACMANUS hydrothermal field on the crest of the felsic Pual Ridge to examine the vertical and lateral variations in mineralization and alteration patterns. We present new data on clay mineral assemblages, clay and whole rock chemistry and clay mineral strontium and oxygen isotopic compositions of altered rocks from a site of diffuse low-temperature venting (Snowcap, Site 1188) and a site of high-temperature venting (Roman Ruins, Site 1189) in order to investigate the water-rock reactions and associated elemental exchanges. The volcanic succession at Snowcap has been hydrothermally altered, producing five alteration zones: (1) chlorite+/-illite-cristobalite-plagioclase alteration apparently overprinted locally by pyrophyllite bleaching at temperatures of 260-310°C; (2) chlorite+/-mixed-layer clay alteration at temperatures of 230°C; (3) chlorite and illite alteration; (4) illite and chlorite+/-illite mixed-layer alteration at temperatures of 250-260°C; and (5) illite+/-chlorite alteration at 290-300°C. Felsic rocks recovered from two holes (1189A and 1189B) at Roman Ruins, although very close together, show differing alteration features. Hole 1189A is characterized by a uniform chlorite-illite alteration formed at ~250°C, overprinted by quartz veining at 350°C. In contrast, four alteration zones occur in Hole 1189B: (1) illite+/-chlorite alteration formed at ~300°C; (2) chlorite+/-illite alteration at 235°C; (3) chlorite+/-illite and mixed layer clay alteration; and (4) chlorite+/-illite alteration at 220°C. Mass balance calculations indicate that the chloritization, illitization and bleaching (silica-pyrophyllite assemblages) alteration stages are accompanied by different chemical changes relative to a calculated pristine precursor lava. The element Cr appears to have a general enrichment in the altered samples from PACMANUS. The clay concentrate data show that Cr and Cu are predominantly present in the pyrophyllites. Illite shows a significant enrichment for Cs and Cu relative to the bulk altered samples. Considerations of mineral stability allow us to place some constraints on fluid chemistry. Hydrothermal fluid pH for the chloritization and illitization was neutral to slightly acidic and relatively acidic for the pyrophyllite alteration. In general the fluids, especially from Roman Ruins and at intermediate depths below Snowcap, show only a small proportion of seawater mixing (<10%). Fluids in shallow and deep parts of the Snowcap holes, in contrast, show stronger seawater influence.

Formato

application/zip, 18 datasets

Identificador

https://doi.pangaea.de/10.1594/PANGAEA.710756

doi:10.1594/PANGAEA.710756

Idioma(s)

en

Publicador

PANGAEA

Direitos

CC-BY: Creative Commons Attribution 3.0 Unported

Access constraints: unrestricted

Fonte

Supplement to: Lackschewitz, Klas S; Devey, Colin W; Stoffers, Peter; Botz, Reiner; Eisenhauer, Anton; Kummetz, M; Schmidt, Mark; Singer, A (2004): Mineralogical, geochemical and isotopic characteristics of hydrothermal alteration processes in the active, submarine, felsic-hosted PACMANUS field, Manus Basin, Papua New Guinea. Geochimica et Cosmochimica Acta, 68(21), 4405-4427, doi:10.1016/j.gca.2004.04.016

Palavras-Chave #1/Sr; 1/Sr ratio; 193-1188A; 193-1188F; 193-1189A; 193-1189B; 87Sr/86Sr; 87Sr/86Sr e; Al2O3; Aluminium oxide; anhydrite; Ba; Barium; Bismarck Sea; Ca; Caesium; Calcium; Calcium oxide; Calculated; CaO; Ce; Cerium; Chl; Chlorite; chlorite-smectite mixed-layer; chlorite-vermiculite mixed-layer; chlorite-vermiculite mixed-layer (% chlorite); Chromium; Co; Cobalt; Copper; Cr; cristobalite; Cs; Cu; d18O; delta 18O; Depth; DEPTH, sediment/rock; DRILL; Drilling/drill rig; Dy; Dysprosium; Electron microprobe; Er; Erbium; Eu; Eu/Eu*; Europium; Europium anomaly; Event; Fe2O3; FeO; Ga; Gadolinium; Gallium; Gd; Hafnium; Hf; Ho; Holmium; ICP-MS, Inductively coupled plasma - mass spectrometry; Ill; illite; Illite; illite-chlorite mixed-layer; illite-chlorite mixed-layer (% illite); illite-smectite-chlorite mixed-layer; illite-smectite mixed-layer (% illite); illite-vermiculite mixed-layer (% illite); interlayered; Iron oxide, Fe2O3; Iron oxide, FeO; isotopic temperature of mineral formation; d18O of DESMOS fluids +0.3per mil; isotopic temperature of mineral formation; d18O of hydrothermal fluids +2.0per mil; isotopic temperature of mineral formation; d18O of seawater 0per mil; Joides Resolution; K2O; K-feldspar; La; Label; Lanthanum; Lead; Leg193; Lu; Lutetium; Mag; Magnesium oxide; Magnetite; Manganese oxide; Mass spectrometer Finnigan MAT 251; Mass spectrometer Finnigan MAT 262 RPQ Plus; MgO; Min assembl; Mineral assemblage; Minerals; MnO; Na2O; Nb; Nd; Nd/Yb; Neodymium; Neodymium/Ytterbium ratio; Ni; Nickel; Niobium; normative ratio; Ocean Drilling Program; ODP; ODP sample designation; P2O5; Pb; Phosphorus oxide; Pl; Plagioclase; Potassium oxide; Pr; Praseodymium; Py; Pyrite; pyrophyllite; Quartz; Qz; Rb; Rubidium; Samarium; Sample code/label; Sample type; Samp type; Sc; Scandium; Silicon dioxide; SiO2; Sm; Sme; Smectite; Sodium oxide; Sr; Strontium; Strontium 87/Strontium 86, error; Strontium 87/Strontium 86 ratio; Sum; Ta; Talc; Tantalum; Tb; T cal; Temperature, calculated; Terbium; Th; Thallium; Thorium; Thulium; TiO2; Titanium oxide; Tl; Tlc; Tm; U; Uranium; V; Vanadium; X-ray diffraction (XRD); Y; Yb; Ytterbium; Yttrium; Zinc; Zirconium; Zn; Zr
Tipo

Dataset