Vein and Karst Barite Deposits in the Western Jebilet of Morocco: Fluid Inclusion and Isotope (S, O, Sr) Evidence for Regional Fluid Mixing Related to Central Atlantic Rifting

Numerous vein and karst barite deposits are hosted by Hercynian basement and Triassic rocks of the western Jebilet in Morocco. Sulfur, oxygen, and strontium isotope analyses of barite, combined with fluid inclusion microthermometry on barite, quartz, and calcite were used to reveal the nature and source of the ore-forming fluids and constrain the age of mineralization. The δ 34S values of barite between 8.9 and 14.7 per mil are intermediate between the sulfur isotope signatures of Triassic evaporites and Triassic-Jurassic seawater and lighter \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(SO_{4}^{2{\mbox{--}}}\) \end{document}, probably derived from the oxidation of dissolved H2S and leaching of sulfides in the Hercynian basement. The 87Sr/86Sr ratios of barite between 0.7093 and 0.7130 range between the radiogenic strontium isotope compositions of micaceous shale and sandstone and the nonradiogenic isotopic signature of Triassic to Jurassic seawater and Cambrian limestone. The δ 18O values of barite between 11 and 15 per mil (SMOW) support mixing between two or more fluids, including Late Triassic to Jurassic seawater or a water dissolving Triassic evaporites along its flow path, hot basinal, or metamorphic fluids with δ 18O values higher than 0 per mil and/or meteoric fluids with δ 18O values lower than 0 per mil. The general trend of decreasing homogenization temperatures and initial ice melting temperatures with increasing salinities of H2O-NaCl ± CaCl2 fluid inclusions trapped in barite, quartz, and calcite indicates that a deep and hot basinal fluid with salinities lower than 6 wt percent NaCl equiv might have mixed with a cooler surficial solution with a mean salinity of 20 wt percent NaCl equiv. Calcium was leached from the Cambrian limestone and the clastic and mafic volcanic rocks of the Hercynian basement. Alkali feldspars and micas contained in the Cambrain sandstones provided most of the Ba to the hydrothermal system. Vein and karst deposits are modeled as a two-component mixing process in which the temperature and the S and Sr isotope composition of the end members changed during the 220 to 155 Ma interval. The hot basinal fluid remained volumetrically dominant during the entire mineralization process. Differences in mean S, O, and Sr isotope compositions among the barite families are interpreted as reflecting differences in mineralization age. Most barite deposits formed before the Kimmeridgian, except for north-south-oriented vein barite, karst barite, and barite cement in the conglomeratic Upper Jurassic, which were deposited later, possibly around 155 Ma. Similar genetic processes have been described for late Paleozoic to Mesozoic F-Ba vein deposits in western Europe. The vein and karst barite in the western Jebilet of Morocco reveals a wide-scale regional mineralization event related to Central Atlantic rifting.

[1]  T. Peryt,et al.  Secular Variation in Seawater Chemistry During the Phanerozoic As Indicated By Brine Inclusions in Halite , 1998, The Journal of Geology.

[2]  D. Kontak,et al.  Aqueous and liquid petroleum inclusions in barite from the Walton Deposit, Nova Scotia, Canada; a Carboniferous, carbonate-hosted Ba-Pb-Zn-Cu-Ag deposit , 1998 .

[3]  H. Taylor Oxygen and hydrogen isotope relationships in hydrothermal mineral deposits , 1997 .

[4]  J. Hanor Origin of saline fluids in sedimentary basins , 1994, Geological Society, London, Special Publications.

[5]  R. Goldstein,et al.  Systematics of fluid inclusions in diagenetic minerals , 1994 .

[6]  A. Felmy,et al.  The solubility of (Ba,Sr)SO4 precipitates: Thermodynamic equilibrium and reaction path analysis , 1993 .

[7]  J. Hoefs,et al.  Effects of mineral precipitation on the sulfur isotope composition of hydrothermal solutions , 1993 .

[8]  À. Canals,et al.  Strontium and sulphur isotope geochemistry of low-temperature barite-fluorite veins of the Catalonian Coastal Ranges (NE Spain): a fluid mixing model and age constraints , 1993 .

[9]  N. Clauer,et al.  Strontium isotopic compositions and potassium and rubidium contents of formation waters in sedimentary basins: Clues to the origin of the solutes , 1993 .

[10]  G. Stampfli,et al.  From rifting to passive margin: the examples of the Red Sea, Central Atlantic and Alpine Tethys , 1992 .

[11]  A. Williams-Jones,et al.  A model for epigenetic Ba-Pb-Zn mineralization in the Appalachian thrust belt, Quebec; evidence from fluid inclusions and isotopes , 1992 .

[12]  C. Ayora,et al.  Origin of the Atrevida Vein (Catalonian coastal ranges, Spain); mineralogic, fluid inclusion, and stable isotope study , 1992 .

[13]  J. Locutura,et al.  Fluid inclusion and geochemical evidence for fluid mixing in the genesis of Ba-F (Pb-Zn) lodes of the Spanish Central System , 1991, Mineralogical Magazine.

[14]  D. Dahl,et al.  Construction of the Triassic and Jurassic portion of the Phanerozoic curve of seawater 87Sr/86Sr , 1990 .

[15]  Michael G. Jones,et al.  The 87Sr86Sr values of Canadian Shield brines and fracture minerals with applications to groundwater mixing, fracture history, and geochronology , 1990 .

[16]  J. Hanor,et al.  Calcite and iron sulfide cementation of Miocene sediments flanking the West Hackberry salt dome, southwest Louisiana, U.S.A. , 1988 .

[17]  R. Bodnar,et al.  Systematics of stretching of fluid inclusions; II, Barite at 1 atm confining pressure , 1988 .

[18]  C. Ramboz,et al.  Temperature, pressure, burial history, and paleohydrology of the Les Malines, Pb-Zn deposit; reconstruction from aqueous inclusions in barite , 1988 .

[19]  R. Bodnar,et al.  Synthetic fluid inclusions. V. Solubility relations in the system NaCl-KCl-H2O under vapor-saturated conditions , 1988 .

[20]  N. Møller,et al.  The prediction of mineral solubilities in natural waters: A chemical equilibrium model for the Na-Ca-Cl-SO4-H2O system, to high temperature and concentration , 1988 .

[21]  H. Behr,et al.  Fluid inclusion characteristics of the Variscan and post-Variscan mineralizing fluids in the Federal Republic of Germany , 1987 .

[22]  R. Bodnar,et al.  Synthetic fluid inclusions in natural quartz I. Compositional types synthesized and applications to experimental geochemistry , 1984 .

[23]  R. Bodnar,et al.  Systematics of stretching of fluid inclusions; I, Fluorite and sphalerite at 1 atmosphere confining pressure , 1984 .

[24]  R. E. Denison,et al.  Variation of seawater 87Sr/86Sr throughout Phanerozoic time , 1982 .

[25]  H. Sakai,et al.  The age curves of sulfur and oxygen isotopes in marine sulfate and their mutual interpretation , 1980 .

[26]  C. Rees Sulphur isotope measurements using SO2 and SF6 , 1978 .

[27]  C. Blount Barite solubilities and thermodynamic quantities up to 300 degrees C and 1400 bars , 1977 .

[28]  B. Robinson,et al.  Oxygen and sulfur isotope equilibria in the BaSO4HSO4−H2O system from 110 to 350°C and applications☆ , 1977 .

[29]  A. B. Carpenter,et al.  Preliminary Report on the Origin and Chemical Evolution of Lead-and Zinc-Rich Oil Field Brines in Central Mississippi , 1974 .

[30]  J. Miller,et al.  Two sources of error in low temperature inclusion homogenization determination, and corrections on published temperatures for the East Tennessee and Laisvall deposits , 1973 .

[31]  H. Sakai,et al.  Elimination of memory effects in 18O/16O determinations in sulphates , 1971 .

[32]  J. Hanor Frequency distribution of compositions in the barite-celestite series , 1968 .

[33]  K. Emery,et al.  The Geology of the Atlantic Ocean , 1967 .