Meteoric fluid‐rock interaction in Variscan shear zones     

Camille Dussaux  Aude Gbelin  Philippe Boulvais  Vronique Gardien  Stephen Grimes  Andreas Mulch 《地学学报》2019,31(4):366-372

Variscan shear zones in the Armorican Massif represent sites of strong fluid‐rock interaction. The hydrogen isotope composition of muscovite (δD_Ms) from syntectonic leucogranite allows to determine the source of fluids that infiltrated the footwall of three detachment zones and the South Armorican Shear Zone. Using temperatures of hydrogen isotope exchange estimated from microstructural data, we calculate the hydrogen isotope ratios of water (δD_water) present within the shear zones during high‐temperature deformation. A ~40‰ difference in δD_water values from deep to shallow crustal level reveals a mixing relationship between deep crustal fluids with higher δD values that range from ?34 to ?33‰, and meteoric fluids with δD values as low as ?74‰ in the upper part of detachment footwalls.  相似文献   

Dissolution–precipitation processes governing the carbonation and silicification of the serpentinite sole of the New Caledonia ophiolite     

Marc?UlrichEmail author  Manuel?Mu?oz  Stéphane?Guillot  Michel?Cathelineau  Christian?Picard  Benoit?Quesnel  Philippe?Boulvais  Clément?Couteau 《Contributions to Mineralogy and Petrology》2014,167(1):952

The weathering of mantle peridotite tectonically exposed to the atmosphere leads commonly to natural carbonation processes. Extensive cryptocrystalline magnesite veins and stock-work are widespread in the serpentinite sole of the New Caledonia ophiolite. Silica is systematically associated with magnesite. It is commonly admitted that Mg and Si are released during the laterization of overlying peridotites. Thus, the occurrence of these veins is generally attributed to a per descensum mechanism that involves the infiltration of meteoric waters enriched in dissolved atmospheric CO₂. In this study, we investigate serpentinite carbonation processes, and related silicification, based on a detailed petrographic and crystal chemical study of serpentinites. The relationships between serpentine and alteration products are described using an original method for the analysis of micro-X-ray fluorescence images performed at the centimeter scale. Our investigations highlight a carbonation mechanism, together with precipitation of amorphous silica and sepiolite, based on a dissolution–precipitation process. In contrast with the per descensum Mg/Si-enrichment model that is mainly concentrated in rock fractures, dissolution–precipitation process is much more pervasive. Thus, although the texture of rocks remains relatively preserved, this process extends more widely into the rock and may represent a major part of total carbonation of the ophiolite.  相似文献   

Fluid migration at the basement/sediment interface along the margin of the Southeast basin (France): implications for Pb–Zn ore formation     

Luc Aquilina  Philippe Boulvais  Jean-Rémi Mossmann 《Mineralium Deposita》2011,46(8):959-979

This study investigates the isotopic composition (C, O, S and Sr) of carbonates, sulphates and sulphide cements in the rock matrix and fracture fillings in geological formations of the Southeast basin of France, using core samples collected during the Deep Geology of France programme (GPF Ardèche theme). The Southeast basin belongs to the Alpine Tethyan margin. It is one of the thickest sedimentary basins in Europe, reaching upwards of 9 km in certain locations. The main fluid transfer from the basin is related to the large Pb–Zn Mississippi Valley-type district along the southern margin of the Massif Central block. A synthesis of the tectonic, mineralogical and petrographic investigations on the GPF boreholes shows that a major fluid circulation event occurred across the Alpine margin of Tethys during the Early Jurassic (Hettangian–Bathonian). It produced a general cementation of the rock porosity through precipitation of dolomite, sulphate and barite. Fracture fillings yield isotopic signatures distinct from the matrix cements. Matrix cements have particular characteristics, i.e. δ³⁴S and δ¹³C that agree with a marine origin. The δ³⁴S values of Permo-Carboniferous to Triassic sulphides from fracture cements are interpreted as resulting from the thermo-chemical reduction of sulphates. Fracture sulphates in the same geological formations yield δ³⁴S values that define a relatively homogeneous end-member, whose composition is similar to sulphates in the Largentière Pb–Zn ore deposit. The source of S is attributed to the Permo-Carboniferous succession. The borehole fracture fillings are attributed to a major fluid circulation stage compatible with the Early Jurassic stage identified from the geological investigation of the boreholes. The formation of the Largentière deposit is considered as resulting from the mixing of this Early Jurassic fluid with continental hydrothermal fluids circulating in a basement horst, along its margin with the sedimentary basin. Other Pb–Zn deposits may also be related to fluid migration along the basement/sedimentary cover interface in the eastern and western parts of the Massif Central. This regional fluid circulation event may represent a geodynamic marker of the Jurassic extensional phase.  相似文献   

Cementation of kerogen-rich marls by alkaline fluids released during weathering of thermally metamorphosed marly sediments. Part I: Isotopic (C,O) study of the Khushaym Matruk natural analogue (central Jordan)     

Serge Fourcade  Laurent Trotignon  Philippe Boulvais  Isabelle Techer  Marcel Elie  Didier Vandamme  Elias Salameh  Hani Khoury 《Applied Geochemistry》2007

The Khushaym Matruk site in central Jordan may represent a natural analogue depicting the interaction of alkaline solutions with a clayey sedimentary formation or with clay-rich confining barriers at the interface with concrete structures in waste disposal sites. In this locality, past spontaneous combustion of organic matter in a clayey biomicritic formation produced a ca. 60 m-thick layer of cement-marble containing some of the high-temperature phases usually found in industrial cements (e.g., spurrite, brucite, and Ca-aluminate). A vertical cross-section of the underlying sediments was used in order to study the interaction between cement-marbles and neighbouring clayey limestones under weathering conditions. A thermodynamic approach of the alteration parageneses (calcite–jennite–afwillite–brucite and CSH phases) in the cement-marbles constrains the interacting solutions to have had pH-values between 10.5 and 12. Over 3 m, the sediments located beneath the metamorphic unit were compacted and underwent carbonation. They display large C and O isotopic variations with respect to “pristine” sediments from the bottom of the section. Low δ¹³C-values down to −31.4‰/PDB show the contribution of CO₂ derived from the oxidization of organic matter and from the atmosphere to the intense carbonation process affecting that particular sedimentary level. The size of the C isotopic anomalies, their geometrical extent and their coincidence with the variations of other markers like the Zn content, the structure of organic matter, the mineralogical composition, all argue that the carbonation process was induced by the percolation of high pH solutions which derived from the alteration of cement-marbles. The temperature of the carbonation process remains conjectural and some post-formation O isotopic reequilibration likely affected the newly-formed carbonate. Carbonation induced a considerable porosity reduction, both in fractures and matrixes. The Khushaym Matruk site may have some bearing to the early life of a repository site, when water saturation of the geological formations hosting the concrete structures is incomplete, enabling simultaneous diffusion of alkaline waters and gaseous CO₂ in the near field.  相似文献   

Cementation of kerogen-rich marls by alkaline fluids released during weathering of thermally metamorphosed marly sediments. Part II: Organic matter evolution,magnetic susceptibility and metals (Ti,Cr, Fe) at the Khushaym Matruk natural analogue (Central Jordan)     

Marcel Elie  Isabelle Techer  Laurent Trotignon  Hani Khoury  Elias Salameh  Didier Vandamme  Philippe Boulvais  Serge Fourcade 《Applied Geochemistry》2007

Spontaneous combustion, less than 1 Ma ago, affected a 60-m thick sediment pile of biomicrite at the Khushaym Matruck site (Jordan). The present study shows that three retrograde alteration stages occurred: weathering, thermal stress and oxidative alkaline perturbation. μ-FT-i.r. spectra of isolated kerogens and oxygen index of whole rocks indicate that oxidation of organic matter occurred down to ∼10 m beneath the metamorphosed zone at Khushaym Matruck. The occurrence of the oxidative weathering bacterially mediated, as suggested by the mass chromatograms of saturated hydrocarbons, can explain high Rock-Eval T_max values and low petroliferous potential measured along the sedimentary pile. On the other hand, the thermal extent of combustion events was limited to the first 2 m from the contact. The mean reflectance of 0.20–0.24% and porosity of ca. 50% of the grey clayey biomicrites indicate that organic matter was very immature and sediments were unconsolidated at the time of the combustion event. Using mineralogy, microscopic analyses of vegetable debris and magnetic susceptibility, a suite of characteristic points corresponding to the thermal imprint can be assessed: (i) x = 0m, T ∼ 1000 °C, (ii) x = 1 m, T ∼ 350 °C, (iii) x = 2 m, T ∼ 150 °C and (iv) x > ∼ 8 m, T ∼ 30 °C. Paleocirculation of meteoric groundwater in the ‘cement-marbles’ generated high-pH fluids that have circulated via fractures and through the matrix porosity of the underlying biomicrites but have also induced alkaline hydrolysis and oxidative attack of the organic matter. The polysaccharide/lignin ratio derived from μ-FT-i.r. analyses shows that the delignification of vegetable debris and degradation of polysaccharides progressively decline in the indurated zone, which indicates a decrease in the pH of migrating solutions. The latter also severely oxidized organic matter at 2.10 and 3.05 m as revealed by the oxygen index and induced the generation of bitumen. The spatial correlation between the oxidation levels of organic matter and the metal contents (Fe, Ti and Cr) suggests that redox reactions were responsible for the immobilization of metals in the indurated biomicrites. The intensity of these reactions is attributed to changes in the fluid flow regime within the sedimentary column.  相似文献   

New U-Pb zircon and Ar/Ar muscovite age constraints on the emplacement of the Lizio syn-tectonic granite (Armorican Massif, France)     

Romain Tartèse  Marc Poujol  Gilles Ruffet  Philippe Boulvais  Philippe Yamato  Jan Košler 《Comptes Rendus Geoscience》2011,343(7):443-453

LA-ICP-MS U-Pb analyses performed on zircon grains from the Lizio granite yielded an emplacement age of 316 ± 6 Ma. Typical S-C structures show that the Lizio granite was emplaced contemporaneously with dextral shearing along the northern branch of the South Armorican Shear Zone and that it was therefore active at that time. ⁴⁰Ar/³⁹Ar analyses performed on muscovite grains yielded plateau dates ranging between 311.5 and 308.2 Ma. Muscovite chemistry is typical of primary magmatic muscovite, which precludes a late fluids-induced resetting of the K-Ar isotopic system. ⁴⁰Ar/³⁹Ar dates thus likely correspond to the cooling ages below the argon closure temperature. Considering the uncertainties on the measured ages, we can propose that either the Lizio granite cooled down quickly in less than a million of years or that it remained in a hot environment for several millions of years after its emplacement. This latter scenario could have been sustained by shear heating during dextral shearing along the northern branch of the South Armorican Shear Zone.  相似文献   

Disturbance versus preservation of U–Th–Pb ages in monazite during fluid–rock interaction: textural, chemical and isotopic in situ study in microgranites (Velay Dome, France)     

A. Didier  V. Bosse  P. Boulvais  J. Bouloton  J.-L. Paquette  J.-M. Montel  J.-L. Devidal 《Contributions to Mineralogy and Petrology》2013,165(6):1051-1072

Monazite is extensively used to date crustal processes and is usually considered to be resistant to diffusive Pb loss. Nevertheless, fluid-assisted recrystallisation is known to be capable of resetting the monazite chronometer. This study focuses on chemical and isotopic disturbances in monazite grains from two microgranite intrusions in the French Central Massif (Charron and Montasset). Petrologic data and oxygen isotopes suggest that both intrusions have interacted with alkali-bearing hydrothermal-magmatic fluids. In the Charron intrusion, regardless of their textural location, monazite grains are sub-euhedral and cover a large domain of compositions. U–Pb chronometers yield a lower intercept age of 297 ± 4 Ma. An inherited component at 320 Ma is responsible for the scattering of the U–Th–Pb ages. The Montasset intrusion was later affected by an additional F-rich crustal fluid with crystallisation of Ca-REE-fluorocarbonates, fluorite, calcite and chloritisation. Pristine monazite is chemically homogeneous and displays ²⁰⁸Pb/²³²Th and ²⁰⁶Pb/²³⁸U concordant ages at 307 ± 2 Ma. By contrast, groundmass monazite shows dissolution-recrystallisation features associated with apatite and thorite precipitation (Th-silicate) and strong chemical reequilibration. ²⁰⁸Pb/²³²Th ages are disturbed and range between 270 and 690 Ma showing that the Th/Pb ratio is highly fractionated during the interaction with fluids. Apparent U–Pb ages are older due to common Pb incorporation yielding a lower intercept age at 312 ± 10 Ma, the age of the pristine monazite. These results show that F-rich fluids are responsible for Th mobility and incorporation of excess Pb, which thus strongly disturbed the U–Th–Pb chronometers in the monazite.  相似文献   

Tracing interactions between natural argillites and hyper-alkaline fluids from engineered cement paste and concrete: Chemical and isotopic monitoring of a 15-years old deep-disposal analogue     

I. Techer  D. Bartier  Ph. Boulvais  E. Tinseau  K. Suchorski  J. Cabrera  A. Dauzères 《Applied Geochemistry》2012

Samples of Toarcian argillite were collected both next to and far from a CEM II cement paste and a CEM II concrete, within the specific context of a 15-a old borehole located in the Tournemire Experimental Platform (Aveyron, France). The objectives were evaluation of the mineralogical and geochemical changes of the claystone at the contact with the cementitious materials and determination of the spatial extent of the interactions. The approach includes the examination of the mineralogical (XRD, SEM, TEM), chemical (major, trace, rare earth elements) and isotopic (Sr, C, O) compositions of argillite whole-rocks and of various soluble phases, at two scales: in the rock matrix (P1 scale) and along micro-cracks (P2 scale). The two study scales outline nearly similar mineralogical modifications, shown by the presence of Ca silicate hydrates (C–S–H) and newly-formed CaCO₃ within 10–15 mm of the cement paste and concrete. Chemical data from whole-rock argillites indicate few changes in a slightly thicker zone (18–20 mm), mainly consisting of an increase in the CaO wt.%, and a decrease in Sr contents. The other elementary contents remained quite constant except for MgO, which suggests redistribution with precipitation of a Mg-rich mineral phase at 20 mm from cement paste/concrete interface. Acetic acid leachates had more pronounced variations, including a decrease of the total elementary content in the same ‘geochemical disturbed zone’ (GDZ), together with a significant increase of the Sr isotopic ratios. A combination of Sr and C/O isotopic patterns was used to distinguish the behavior of secondary cementitious phases in the clay-rich rock: (i) calcite dissolution and re-precipitation is supported by C/O isotopic data and (ii) C–S–H neoformation is evidenced by the ⁸⁷Sr/⁸⁶Sr ratios; this tool also contributes to determine the origin of the fluids. The proportion of newly-formed C–S–H in the matrix and in the micro-cracks of the argillite is modeled.  相似文献   

Persistence of pre-metamorphic C and O isotopic signatures in marbles subject to Pan-African granulite-facies metamorphism and U–Th mineralization (Tranomaro, Southeast Madagascar)     

P. Boulvais  S. Fourcade  G. Gruau  B. Moine  M. Cuney 《Chemical Geology》1998,150(3-4):247-262

The status of fluid regimes during the Pan-African granulite-facies metamorphism in Southern Madagascar was examined by means of a mineralogical and stable isotope study of marble lithologies. In the granulitic Tranomaro area, which is made up of metasedimentary rocks (metapelitic, leptynitic (felsic) and calc–silicate metasediments) and intruded by syn-granulitic granitic bodies, syn-granulitic mineralization (Th–U) and metasomatic transformations (marbles→pyroxenites) demonstrate that fluid circulation has occurred. The Tranomaro marbles can be subdivided into two compositional groups, either Mg-poor or Mg-rich. This division reflects pre-metamorphic compositional differences rather than different histories. On a regional scale, the marbles display a large variation in (from +19 to +6.5‰ relative to SMOW) but have a more restricted range (from +1.4 to −2.5‰ relative to PDB). The lowest values are observed in magnesian marbles, whereas calcic ones do not have values lower than +13.5‰. Both initially low and high marbles may have locally been infiltrated by the syn-metamorphic fluid flow which gave rise to pyroxenites and Th–U ores (thorianite). values of carbonate in Mg-rich marbles evolve from +7 up to 8.5‰ towards the contact with a metasomatic pyroxenite in a meter-scale profile across an infiltration zone. The mineralogy, as well as the large and small-scale isotopic results argue for: (i) a pre-metamorphic origin for the isotopic variations, probably related to pre-granulitic dolomitization, (ii) a lack of pervasive fluid infiltration capable of erasing pre-metamorphic isotopic compositional differences, (iii) an absence of mantle-derived C-bearing fluids in the infiltrated zones. For the area as a whole, the present data are consistent with the decarbonation of impure siliceous limestones and dolostones coupled with fluid release from syn-metamorphic granitic intrusions.  相似文献   

Metallogeny of precious and base metal mineralization in the Murchison Greenstone Belt, South Africa: indications from U–Pb and Pb–Pb geochronology     

J. Jaguin  M. Poujol  P. Boulvais  L. J. Robb  J. L. Paquette 《Mineralium Deposita》2012,47(7):739-747

The 3.09 to 2.97 Ga Murchison Greenstone Belt is an important metallotect in the northern Kaapvaal Craton (South Africa), hosting several precious and base metal deposits. Central to the metallotect is the Antimony Line, striking ENE for over 35?km, which hosts a series of structurally controlled Sb–Au deposits. To the north of the Antimony Line, hosted within felsic volcanic rocks, is the Copper–Zinc Line where a series of small, ca. 2.97 Ga Cu–Zn volcanogenic massive sulfide (VMS)-type deposits occur. New data are provided for the Malati Pump gold mine, located at the eastern end of the Antimony Line. Crystallizations of a granodiorite in the Malati Pump Mine and of the Baderoukwe granodiorite are dated at 2,964?±?7 and 2,970?±?7?Ma, respectively (zircon U–Pb), while pyrite associated with gold mineralization yielded a Pb–Pb age of 2,967?±?48?Ma. Therefore, granodiorite emplacement, sulfide mineral deposition and gold mineralization all happened at ca. 2.97?Ga. It is, thus, suggested that the major styles of orogenic Au–Sb and the Cu–Zn VMS mineralization in the Murchison Greenstone Belt are contemporaneous and that the formation of meso- to epithermal Au–Sb mineralization at fairly shallow levels was accompanied by submarine extrusion of felsic volcanic rocks to form associated Cu–Zn VMS mineralization.  相似文献