Details
Original language | English |
---|---|
Pages (from-to) | 217-239 |
Number of pages | 23 |
Journal | Mineralium deposita |
Volume | 45 |
Issue number | 3 |
Publication status | Published - Mar 2010 |
Externally published | Yes |
Abstract
The Spessart district (SW Germany), located at the southwestern margin of the Permian Kupferschiefer basin in Central Europe, hosts abundant stratabound and structurally controlled base metal mineralization. The mineralization styles identified are (1) stratabound Cu-Pb-Zn-(Ag) ores in Zechstein sedimentary rocks, (2) structurally controlled Cu-As-(Ag) ores in Zechstein sedimentary rocks, (3) crosscutting Co-Ni-(Bi)-As and Cu-Fe-As veins, (4) stratabound metasomatic Fe-Mn carbonate ores in Zechstein dolomite, (5) barren barite veins, and (6) Fe-Mn-As veins in Permian rhyolites. Building on previous work that involved mineralogical, textural, and chemical characterization of the major mineralization types, we have performed a comprehensive sulfur isotope study that applied both conventional and novel laser-ablation multi-collector inductively coupled plasma mass spectrometry techniques. The δ34S values of sulfide minerals from the different ore types are consistently negative and highly variable, in the range between -44.5‰ and -3.9‰, whereas the δ34S values of barite are all positive in the range between 4.7‰ and 18.9‰. Remarkably, stratabound and structurally controlled mineralization in Zechstein sedimentary rocks has the least negative δ34S values, whereas vein-type deposits have consistently more negative δ34S values. The observed pattern of sulfide δ34S values can be best interpreted in terms of fluid mixing at the basement-cover interface. Hydrothermal fluids originating from the crystalline basement migrated upward along subvertical fault zones and were periodically injected into groundwaters that were flowing in the post-Variscan sedimentary cover. These groundwaters had interacted with the Zechstein sedimentary rocks, resulting in fluids characterized by elevated concentrations of reduced sulfur (with negative δ34S values) and alkaline pH. Repeated mixing between both chemically contrasting fluids caused rapid and efficient precipitation of sulfide ore minerals in hydrothermal veins with highly variable but distinctly negative δ34S values.
Keywords
- Base metals, Germany, Kupferschiefer, Laser-ablation MC-ICP-MS, Sulfur isotopes
ASJC Scopus subject areas
- Earth and Planetary Sciences(all)
- Geophysics
- Earth and Planetary Sciences(all)
- Geochemistry and Petrology
- Earth and Planetary Sciences(all)
- Economic Geology
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In: Mineralium deposita, Vol. 45, No. 3, 03.2010, p. 217-239.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - The role of the Kupferschiefer in the formation of hydrothermal base metal mineralization in the Spessart ore district, Germany
T2 - Insight from detailed sulfur isotope studies
AU - Wagner, Thomas
AU - Okrusch, Martin
AU - Weyer, Stefan
AU - Lorenz, Joachim
AU - Lahaye, Yann
AU - Taubald, Heiner
AU - Schmitt, Ralf T.
N1 - Funding information: This project was made possible by funding from the German Research Council (DFG). The mineral concentrates were carefully prepared by Maria Kirchenbaur (Würzburg). Uli Schüssler (Würzburg) is thanked for his help and assistance during electron-microprobe analysis. The conventional sulfur isotope analyses were performed with the assistance of Bernd Steinhilber (Tübingen), whose help is gratefully acknowledged. Further thanks are due to Klaus-Peter Kelber (Würzburg) for the microphotographs and Peter Späthe (Würzburg) for the preparation of the polished sections. Adrian Boyce and Bernd Lehmann are thanked for their constructive comments that have helped to improve our paper.
PY - 2010/3
Y1 - 2010/3
N2 - The Spessart district (SW Germany), located at the southwestern margin of the Permian Kupferschiefer basin in Central Europe, hosts abundant stratabound and structurally controlled base metal mineralization. The mineralization styles identified are (1) stratabound Cu-Pb-Zn-(Ag) ores in Zechstein sedimentary rocks, (2) structurally controlled Cu-As-(Ag) ores in Zechstein sedimentary rocks, (3) crosscutting Co-Ni-(Bi)-As and Cu-Fe-As veins, (4) stratabound metasomatic Fe-Mn carbonate ores in Zechstein dolomite, (5) barren barite veins, and (6) Fe-Mn-As veins in Permian rhyolites. Building on previous work that involved mineralogical, textural, and chemical characterization of the major mineralization types, we have performed a comprehensive sulfur isotope study that applied both conventional and novel laser-ablation multi-collector inductively coupled plasma mass spectrometry techniques. The δ34S values of sulfide minerals from the different ore types are consistently negative and highly variable, in the range between -44.5‰ and -3.9‰, whereas the δ34S values of barite are all positive in the range between 4.7‰ and 18.9‰. Remarkably, stratabound and structurally controlled mineralization in Zechstein sedimentary rocks has the least negative δ34S values, whereas vein-type deposits have consistently more negative δ34S values. The observed pattern of sulfide δ34S values can be best interpreted in terms of fluid mixing at the basement-cover interface. Hydrothermal fluids originating from the crystalline basement migrated upward along subvertical fault zones and were periodically injected into groundwaters that were flowing in the post-Variscan sedimentary cover. These groundwaters had interacted with the Zechstein sedimentary rocks, resulting in fluids characterized by elevated concentrations of reduced sulfur (with negative δ34S values) and alkaline pH. Repeated mixing between both chemically contrasting fluids caused rapid and efficient precipitation of sulfide ore minerals in hydrothermal veins with highly variable but distinctly negative δ34S values.
AB - The Spessart district (SW Germany), located at the southwestern margin of the Permian Kupferschiefer basin in Central Europe, hosts abundant stratabound and structurally controlled base metal mineralization. The mineralization styles identified are (1) stratabound Cu-Pb-Zn-(Ag) ores in Zechstein sedimentary rocks, (2) structurally controlled Cu-As-(Ag) ores in Zechstein sedimentary rocks, (3) crosscutting Co-Ni-(Bi)-As and Cu-Fe-As veins, (4) stratabound metasomatic Fe-Mn carbonate ores in Zechstein dolomite, (5) barren barite veins, and (6) Fe-Mn-As veins in Permian rhyolites. Building on previous work that involved mineralogical, textural, and chemical characterization of the major mineralization types, we have performed a comprehensive sulfur isotope study that applied both conventional and novel laser-ablation multi-collector inductively coupled plasma mass spectrometry techniques. The δ34S values of sulfide minerals from the different ore types are consistently negative and highly variable, in the range between -44.5‰ and -3.9‰, whereas the δ34S values of barite are all positive in the range between 4.7‰ and 18.9‰. Remarkably, stratabound and structurally controlled mineralization in Zechstein sedimentary rocks has the least negative δ34S values, whereas vein-type deposits have consistently more negative δ34S values. The observed pattern of sulfide δ34S values can be best interpreted in terms of fluid mixing at the basement-cover interface. Hydrothermal fluids originating from the crystalline basement migrated upward along subvertical fault zones and were periodically injected into groundwaters that were flowing in the post-Variscan sedimentary cover. These groundwaters had interacted with the Zechstein sedimentary rocks, resulting in fluids characterized by elevated concentrations of reduced sulfur (with negative δ34S values) and alkaline pH. Repeated mixing between both chemically contrasting fluids caused rapid and efficient precipitation of sulfide ore minerals in hydrothermal veins with highly variable but distinctly negative δ34S values.
KW - Base metals
KW - Germany
KW - Kupferschiefer
KW - Laser-ablation MC-ICP-MS
KW - Sulfur isotopes
UR - http://www.scopus.com/inward/record.url?scp=77954086952&partnerID=8YFLogxK
U2 - 10.1007/s00126-009-0270-2
DO - 10.1007/s00126-009-0270-2
M3 - Article
AN - SCOPUS:77954086952
VL - 45
SP - 217
EP - 239
JO - Mineralium deposita
JF - Mineralium deposita
SN - 0026-4598
IS - 3
ER -