Metasomatic hydrous fluids in amphibole peridotites from Zabargad Island (Red Sea)     

Pierre Agrinier  Catherine Mvel  Delphine Bosch  Marc Javoy 《Earth and Planetary Science Letters》1993,120(3-4):187-205

Combining textural, petrological, chemical and isotopic (Sr, H and O) data for amphiboles and whole rocks from the Zabargad peridotite diapir allows three different events to be distinguished. During each event, which can be related to a specific tectonic process of the rifting of the Red Sea, hydrous fluids produced amphiboles.

The first and the second generations of amphiboles have characteristics consistent with the involvement of mantle-derived hydrous fluids. The first generation consists of scarce Ti-pargasites which crystallized from small amounts of fluid at temperatures of around 900–1000°C. Their growth was linked to magma percolation in the peridotites before their deformation during diapiric uplift. The second generation consists of Cr-pargasites which crystallized locally (and abundantly) during reaction between the peridotites and a sodium/potassium-bearing hydrous fluid at temperatures of around 700–800°C. These amphiboles grew synchronously with the diapiric uplift. The hydrous fluids probably originated in the sub-continental mantle and were released during the diapiric uplift of the peridotites.

The third generation consists of amphiboles (pargasitic hornblende, hornblende sensu lato and tremolite) which are localized in shear zones and veins. They crystallized at temperatures estimated between 700°C and 450°C, again from a sodium/potassium-bearing hydrous fluid. However, this fluid is extraneous to the peridotites, as shown by the Sr, H and O isotope compositions which suggest seawater penetration either during or after the final emplacement of the peridotite diapir.

Although the peridotite diapir was emplaced in granulitic gneisses of the pan-African deep continental crust, no evidence was found for a contribution of hydrous continental fluids in the production of the amphiboles present in the peridotite bodies of Zabargad Island.  相似文献   

Les eaux thermales des granites de Galice (Espagne): des eaux carbogazeuses aux eaux alcalines (Thermal waters from granites of Galicia (Spain): from CO₂-rich to high-pH waters)     

Gil Michard  Catherine Beaucaire 《Chemical Geology》1993,110(4):345-360

Thermal waters from Galicia, Spain, range from CO₂-rich, low-pH to high-pH, sulfide-rich waters, going through intermediate waters. In order to explain the variations of their chemical composition, we present a discussion of the major factors governing the water composition. We eiscuss especially the isochemical recrystallization of a granite. It is shown that the equilibrium mineral association of the water-alkali granite system is unique. For chalco-alkaline granites, two different associations are possible, depending on the chemical composition of the granite. The effect of an addition of CO₂ is also discussed.

Some criteria allowing a distinction between fully equilibrated and non-equilibrated waters are presented.

Finally, the composition of Galician waters is explained by different initial CO₂ contents and by different values of the degree of the granite-water reaction progress (ξ).

Résumé

Les eaux thermales de Galice (Espagne) vont des eaux riches en CO₂ aux eaux typiquement alcalines en passant par différents intermédiaires. Pour comprendre l'évolution de la composition chimique de ces eaux, nous avons été conduits à discuter, de façon plus générale, des facteurs majeurs qui fixent la composition minéralogique résultant d'une recristallisation isochimique du granite. Nous avons pu montrer que les granites alcalins se transformaient toujours en la même association minérale, tandis que les granites calcoalcalins pouvaient donner naissance à deux associations d'équilibre différentes. L'apport de CO₂ au système eau-roche peut faire passer d'une association minérale à l'autre, et, si le CO₂ est en grande quantité, à une association contenant un minéral de moins et du CO₂ en excès. On propose également, pour les solutions géothermales, des critères d'équilibre ou de non équilibre, basés sur la composition en éléments majeurs. La variation de composition des eaux de Galice peut alors s'interpréter par des teneurs variables en CO₂ et des degrés d'avancement différents de la réaction d'interaction eau-granite.  相似文献   

The solubility of fluorite in hydrothermal solutions,an experimental study     

Catherine K. Richardson  H.D. Holland 《Geochimica et cosmochimica acta》1979,43(8):1313-1325

The solubility of fluorite in NaCl solutions increases with increasing temperature at all ionic strengths up to about 100°C. Above this temperature, the solubility passes through a maximum and possibly a minimum with increasing temperature at NaCl concentrations of 1.0M or less, and increases continuously with increasing temperature at NaCl concentrations above 1.0M. At any given temperature, the solubility of fluorite increases with increasing salt concentration in NaCl, KCl and CaCl₂ solutions. The solubility follows Debye-Hückel theory for KCl solutions. In NaCl and CaCl₂ solutions, the solubility of fluorite increases more rapidly than predicted by Debye-Hückel theory: the excess solubility is due to the presence of NaF^c, CaF⁺, and possibly of Na₂F⁺. The solubility of fluorite in NaCl-CaCl₂ and in NaCl-CaCl₂-MgCl₂ solutions is controlled by the common ion effect and by the presence of NaF^c, CaF⁺, and MgF⁺. The solubility of fluorite in NaCl-HCl solutions increases rapidly with increasing initial HCl concentration; the large solubility increase is due to the presence of HF^c. It seems likely that complexes other than those identified in this study rarely play a major role in fluoride transport and fluorite deposition at temperatures below 300°C.  相似文献   

Fluorite deposition in hydrothermal systems   总被引：1，自引：0，他引：1  

Catherine K. Richardson  H.D. Holland 《Geochimica et cosmochimica acta》1979,43(8):1327-1335

During the formation of fluorite deposits fluorite is precipitated either as a consequence of changes in temperature and pressure along the flow path of hydrothermal solutions or due to fluid mixing, or as the result of the interaction of hydrothermal solutions with wall rocks.A decrease in temperature in the flow direction is the most appealing, though still unproven, mechanism of fluorite deposition in Mississippi Valley fluorite deposits.Mixing can produce solutions which are either undersaturated or supersaturated with respect to fluorite. The most important parameters are the temperature, the salinity, and the calcium and fluoride concentration of the fluids prior to mixing.A variety of wall rock reactions can lead to fluorite precipitation. Among these reactions which increase the pH of initially rather acid (pH ≤ 3) hydrothermal solutions are apt to be particularly important.  相似文献   

Mineral-chemistry and stable-isotope constraints on the magmatism, hydrothermal alteration, and related PGE–(base-metal sulphide) mineralisation of the Mesoarchaean Baula-Nuasahi Complex, India     

Thierry Augé  Catherine Lerouge 《Mineralium Deposita》2004,39(5-6):583-607

The Baula-Nuasahi Complex, on the southern flank of the Singhbhum Archaean nucleus in north-eastern India, exposes a series of Mesoarchaean igneous suites. These are (1) a gabbro–anorthosite unit, which is petrographically homogeneous, although mineral-chemistry data hint at a subtle eastward differentiation; (2) a peridotite unit (with three chromitite layers) together with (3) a pyroxenite unit which display cumulate textures, modal layering, and (for the peridotite unit) differentiation trends in both mineralogy and mineral chemistry; and (4) the Bangur gabbro (~3.1 Ga), which defines an oblong intrusion, crosscutting the older igneous suites in the southern part of the complex, with a curvilinear NW-trending apophysis, 2 km long and up to 40 m wide. Magmatic breccia comprising ultramafic and chromitite wall-rock clasts in a gabbro matrix is exposed at the contact of the main Bangur gabbro body and also forms the entire Bangur gabbro apophysis. Concentrations of platinum-group minerals (PGMs) are found where the breccia contains abundant chromitite clasts, and two types of platinum-group-element (PGE) mineralisation are recognised. Type 1 (Pt 1.1–14.2, Pd 0.1–2.1 ppm, with an average Pt/Pd=8–9) is a contact-type mineralisation which occurs in the breccia at the contact between the Bangur intrusion and its ultramafic host. The PGMs—Pt alloys (isoferroplatinum) and sulphides (braggite, malanite)—are enclosed by pyroxene and plagioclase, reflecting a magmatic origin. Significant wall-rock assimilation by the magma (giving rise to the Bangur gabbro) is indicated by changes in pyroxene composition and by the presence of relicts of chromite (from the host) now altered to secondary ferritchromite in the contact zone. Type 2 PGE mineralisation (Pt 0.3–1.6, Pd 1.8–6.0 ppm, with Pt/Pd~0.5–3.0) is restricted to the breccia apophysis of the Bangur gabbro where it occurs in the breccia matrix, associated with an intense hydrothermal alteration which does not exist in the contact zone. PGMs (PGE arsenides, tellurides, bismuthides and antimonides) and, where present, base-metal sulphides (BMSs) form intergrowths with hydrous silicates, reflecting a hydrothermal origin. Oxygen isotope geothermometry documents the main stages of hydrothermal alteration within a decreasing temperature range between 700–1,000 and 500–600 °C, and oxygen, hydrogen and sulphur isotopes show that the hydrothermal fluids were derived from the magma rather than an external source. Pervasive hydrothermal alteration in the breccia apophysis likely represents upward channelling of late-magmatic fluids along a narrow, near-vertical, subplanar conduit which led away from the main magma chamber. We suggest that Type 2 mineralisation was produced by late-magmatic hydrothermal remobilisation and reconcentration of Type 1 PGE mineralisation, and that the composition of the hydrothermal fluids controlled whether BMSs were enriched along with the PGMs.Editorial handling: P. Lightfoot  相似文献   

Mössbauer spectroscopic determination of Fe<Superscript>3+</Superscript>/Fe<Superscript>2+</Superscript> in synthetic basaltic glass: a test of empirical<Emphasis Type="Italic"> f</Emphasis>O<Subscript>2</Subscript> equations under superliquidus and subliquidus conditions     

Georg?M.?PartzschEmail author  Dominique?Lattard  Catherine?McCammon 《Contributions to Mineralogy and Petrology》2004,147(5):565-580

One of the most widely used methods to estimate magmatic oxygen fugacity involves the use of empirical equations relating fO₂ to the iron redox state in quenched silicate liquids; however none of the equations have been calibrated experimentally under subliquidus conditions at temperatures and oxygen fugacities that are relevant to natural magmas. To address this problem, we tested two empirical relationships [Eq. (1) in Kress and Carmichael 1991; Eq. (6) in Nikolaev et al. 1996] on synthetic glasses synthesized from a ferrobasaltic and a transitional alkali-basaltic composition at sub- to superliquidus temperatures (1,132–1,222°C) and controlled oxygen fugacities (FMQ=–2 to +1.4). Fe³⁺/Fe was determined using conventional and milliprobe Mössbauer spectroscopy, and verified using wet chemical analysis on selected samples. For the ferrobasaltic bulk composition SC1-P, both empirical models reproduce the Fe³⁺/Fe ratio of the quenched liquids generally within 0.03 for sub- as well as superliquidus temperatures, although agreement is worse at higher oxygen fugacities (FMQ>+1) at subliquidus temperatures. For the transitional alkali-basaltic composition 7159V-P, both models reproduce the Fe³⁺/Fe ratio of the quenched liquids generally within 0.04, although agreement is worse for both models at high oxygen fugacities (FMQ>+1). Such behaviour may be related to a change in melt structure, where a progressive change in Fe³⁺ coordination is inferred to occur as a function of Fe³⁺/Fe based on Mössbauer center shifts. Recasting the data in terms of oxygen fugacity shows that calculated oxygen fugacities deviate from those actually maintained during the equilibration of the sample material by generally no more than 0.5 log-bar unit, with maximum deviations that only rarely exceed one log-bar unit.Editorial responsibility: J. Hoefs  相似文献   

Subtidal variability of transverse flow off a cape     

Arnoldo?Valle–LevinsonEmail author  Mary Catherine?Brown 《Ocean Dynamics》2003,53(3):166-175

Time series of velocity profiles at two Chesapeake Bay entrance sites were used to characterize the subtidal variability of transverse flows off a cape. A shallow sampling site was located near Cape Henry over 6 m of water and separated from a deep site, 20 m deep, by a distance of 4 km. The velocity profiles showed that wind-induced subtidal variations in general masked curvature effects (centrifugal accelerations) that may produce secondary circulation associated with tidal flow around a cape. Such secondary circulation, consisting of flow away from the cape at surface and toward the cape at depth, was observed only during periods of weak winds. Most of the time, transverse flows were unidirectional throughout the water column and moved in opposite directions at the two sites examined. This caused convergence of transverse flow between the two sites under the influence of northerly winds and divergence of transverse flow with southwesterly winds. In addition to unidirectional and curvature-induced secondary flows, other modes of subtidal variability consisted of (1) two-layered responses with surface flow toward the cape, and (2) three-layered responses. These two- and three-layered structures were observed more frequently at the deep site, where greater stratification is expected, than at the shallow site.Responsible Editor: Iris Grabemann  相似文献   

Sulphur isotope constraints on formation conditions of the Luiswishi ore deposit, Democratic Republic of Congo (DRC)   总被引：1，自引：0，他引：1  

C. Lerouge  J. Cailteux  A.B. Kampunzu  J.P. Milesi  C. Flhoc 《Journal of African Earth Sciences》2005,42(1-5):173

Luiswishi is a Congo-type Neoproterozoic sediment-hosted stratiform Cu–Co ore deposit of the Central Africa Copperbelt, located northwest of Lubumbashi (DRC). The ores form two main Cu–Co orebodies hosted by the Mines Subgroup, one in the lower part of the Kamoto Formation and the other at the base of the Dolomitic Shales Formation. Sulphides occur essentially as early parallel layers of chalcopyrite and carrolite, and secondarily as late stockwork sulphides cross-cutting the bedding and the early sulphide generation. Both types of stratiform and stockwork chalcopyrite and carrolite were systematically analyzed for sulphur isotopes, along the lithostratigraphic succession of the Mine Series. The quite similar δ³⁴S values of stratiform sulphides and late stockwork sulphides suggest an in situ recrystallization or a slight remobilization of stockwork sulphides without attainment of isotopic equilibrium between different sulphide phases (chalcopyrite and carrolite). The distribution of δ³⁴S values (−14.4‰ to +17.5‰) combined with the lithology indicates a strong stratigraphic control of the sulphur isotope signature, supporting bacterial sulphate reduction during early diagenesis of the host sediments, in a shallow marine to lacustrine environment. Petrological features combined with sulphur isotopic data of sulphides at Luiswishi and previous results on nodules of anhydrite in the Mine Series indicate a dominant seawater/lacustrine origin for sulphates, precluding a possible hydrothermal participation. The high positive δ³⁴S values of sulphides in the lower orebody at Luiswishi, hosted in massive chloritic–dolomitic siltite (known as Grey R.A.T.), fine-grained stratified dolostone (D.Strat.) and silicified-stromatolitic dolomites alternating with chloritic–dolomitic silty beds (R.S.F.), suggest that they were probably deposited during a period of regression in a basin cut off from seawater. The variations of δ³⁴S values (i.e. the decrease of δ³⁴S values from the Kamoto Formation to the overlying Dolomitic Shales and then the slight increase from S.D.2d to S.D.3a and S.D.3b members) are in perfect agreement with the inferred lithological and transgressive–regressive evolution of the ore-hosting sedimentary rocks [Cailteux, J., 1994. Lithostratigraphy of the Neoproterozoic Shaba-type (Zaire) Roan Supergroup and metallogenesis of associated stratiform mineralization. In: Kampunzu A.B., Lubala, R.T. (Eds.), Neoproterozoic Belts of Zambia, Zaire and Namibia. Journal of African Earth Sciences 19, 279–301].  相似文献   

Genesis of sediment-hosted stratiform copper–cobalt deposits, central African Copperbelt   总被引：3，自引：0，他引：3  

J.L.H. Cailteux  A.B. Kampunzu  C. Lerouge  A.K. Kaputo  J.P. Milesi 《Journal of African Earth Sciences》2005,42(1-5):134

The Neoproterozoic central African Copperbelt is one of the greatest sediment-hosted stratiform Cu–Co provinces in the world, totalling 140 Mt copper and 6 Mt cobalt and including several world-class deposits (10 Mt copper). The origin of Cu–Co mineralisation in this province remains speculative, with the debate centred around syngenetic–diagenetic and hydrothermal-diagenetic hypotheses.The regional distribution of metals indicates that most of the cobalt-rich copper deposits are hosted in dolomites and dolomitic shales forming allochthonous units exposed in Congo and known as Congolese facies of the Katangan sedimentary succession (average Co:Cu = 1:13). The highest Co:Cu ratio (up to 3:1) occurs in ore deposits located along the southern structural block of the Lufilian Arc. The predominantly siliciclastic Zambian facies, exposed in Zambia and in SE Congo, forms para-autochthonous sedimentary units hosting ore deposits characterized by lower a Co:Cu ratio (average 1:57). Transitional lithofacies in Zambia (e.g. Baluba, Mindola) and in Congo (e.g. Lubembe) indicate a gradual transition in the Katangan basin during the deposition of laterally correlative clastic and carbonate sedimentary rocks exposed in Zambia and in Congo, and are marked by Co:Cu ratios in the range 1:15.The main Cu–Co orebodies occur at the base of the Mines/Musoshi Subgroup, which is characterized by evaporitic intertidal–supratidal sedimentary rocks. All additional lenticular orebodies known in the upper part of the Mines/Musoshi Subgroup are hosted in similar sedimentary rocks, suggesting highly favourable conditions for the ore genesis in particular sedimentary environments. Pre-lithification sedimentary structures affecting disseminated sulphides indicate that metals were deposited before compaction and consolidation of the host sediment.The ore parageneses indicate several generations of sulphides marking syngenetic, early diagenetic and late diagenetic processes. Sulphur isotopic data on sulphides suggest the derivation of sulphur essentially from the bacterial reduction of seawater sulphates. The mineralizing brines were generated from sea water in sabkhas or hypersaline lagoons during the deposition of the host rocks. Changes of Eh–pH and salinity probably were critical for concentrating copper–cobalt and nickel mineralisation. Compressional tectonic and related metamorphic processes and supergene enrichment have played variable roles in the remobilisation and upgrading of the primary mineralisation.There is no evidence to support models assuming that metals originated from: (1) Katangan igneous rocks and related hydrothermal processes or; (2) leaching of red beds underlying the orebodies. The metal sources are pre-Katangan continental rocks, especially the Palaeoproterozoic low-grade porphyry copper deposits known in the Bangweulu block and subsidiary Cu–Co–Ni deposits/occurrences in the Archaean rocks of the Zimbabwe craton. These two sources contain low grade ore deposits portraying the peculiar metal association (Cu, Co, Ni, U, Cr, Au, Ag, PGE) recorded in the Katangan sediment-hosted ore deposits. Metals were transported into the basin dissolved in water.The stratiform deposits of Congo and Zambia display features indicating that syngenetic and early diagenetic processes controlled the formation of the Neoproterozoic Copperbelt of central Africa.  相似文献   

Undressing the researcher: feminism, embodiment and sexuality at a queer bathhouse event   总被引：2，自引：0，他引：2  

Alison L Bain  Catherine J Nash 《Area》2006,38(1):99-106

In this paper we examine how the researcher's body can be used as a tool for data collection in the process of ethnographic fieldwork. We focus in particular on the tensions inherent in undertaking embodied ethnographic research in the sexualized setting of a queer women's bathhouse event in Toronto, Canada. Our discussion addresses three moments within the research process: preparing our bodies to attend the bathhouse; positioning our bodies within the spaces of the bathhouse; and interacting with our bodies during the event. Through this discussion we argue that the body of the researcher is a contested site of knowledge production.  相似文献