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1.
Summary A detailed electron microprobe study of P, F, Ge and Ga-contents in rock-forming topaz was performed on a suite of Variscan granites at Podlesí in the western Kruné Hory Mts., Czech Republic. Topaz crystals from the relatively less evolved biotite- and protolithionite granites display homogeneous cathodo-luminescence (CL) intensities, whereas topaz from the marginal pegmatite, highly fractionated zinnwaldite granite and greisens show intense oscillatory zoning. Phosphorus contents reach 1.15wt% P2O5 in topaz from the zinnwaldite granite. Many topaz crystals are distinctly zoned with a maximum P content in the transition zone between core and rim. Phosphorus is incorporated into the topaz lattice by berlinite substitution: Al3++P5+=Si4++Si4+. The majority of analysed topazes are highly saturated in F, reaching 90–97% of the theoretical maximum saturation. Topaz from the marginal pegmatite only reaches 87–90% of F-saturation. There is a positive correlation between Ptopaz and Pwhole rock, but no correlation between Ftopaz and Fwhole rock. No difference has been found in P and F contents between magmatic and the hydrothermal (=greisen stage) topaz. Contents of Ge and Ga vary from around the detection limit (50ppm) up to 200ppm Ge and 100ppm Ga, respectively.  相似文献   

2.
Summary A large number of podiform chromitite bodies of massive, disseminated and nodular type have been located in ultramafic units, composed of depleted mantle harzburgite and dunite of the Marmaris Peridotite from Ortaca (Mula, SW Turkey). The chromite ore bodies are surrounded by dunite envelopes of variable thickness, exhibiting transitional boundaries to harzburgite host rocks. Chromitites, containing a large number of inclusions, i.e. silicates, base metal sulphides and alloys, and platinum-group minerals (PGM) have a wide range of chemical composition. The Cr# [Cr/(Cr+Al)] values of most chromitites are high (0.61–0.81) and Mg# [Mg/(Mg+Fe2+)] values range between 0.65 and 0.71 with TiO2 content lower than 0.24wt.%, which may reflect the crystallization of chromites from boninitic magmas in supra-subduction setting environment.Platinum-group minerals (PGM) such as laurite, erlichmanite and Os–Ir alloys, silicates such as olivine, clinopyroxene and amphibole, and base metal sulphides (BM-S), alloys (BM-A) and arsenides (BM-As) are found as inclusions in chromite or in the serpentine matrix. Platinum-group element (PGE) concentrations of the Ortaca chromitites (OC) are low in all samples. Total PGE (Ir+Ru+Rh+Pt+Pd) ranges from 63ng/g to 266ng/g and Pd/Ir ratios range between 0.23 and 4.75. PGE content is higher and the Pd/Ir ratio lower in Cr-rich chromitites compared to Al-rich ones. There is a strong negative correlation between the Cr# and Pd/Ir ratios (r=–0.930). The PGE patterns show a negative slope from Ru to Pt and a positive slope from Pt to Pd. The low PGE content in the majority of the OC may reflect a lack of sulphur saturation during an early stage of their crystallization. The laurite compositions show a wide range of Ru–Os substitution caused by relatively low temperature and increasing f(S2) during the chromite crystallization. The high Cr# of and hydrous silicate mineral inclusions in chromite imply that chromite crystallized in a supra-subduction setting.  相似文献   

3.
Trace hydrogen zoning in diopside   总被引：2，自引：0，他引：2  
Summary ¶The trace hydrogen content of a colourless to light-green zoned diopside single-crystal from Zillertal was investigated by IR microspectroscopy. The light-green part of the crystal reveals pleochroic OH absorption bands centred at 3645, 3463, and 3358cm–1 which are attributed to structural OH defects. The OH absorptions of the colourless crystal part are characterised by weak bands at 3645 and 3662cm–1 and by a strong band at 3676cm–1. The bands at 3662 and 3676cm–1 are attributed to the presence of amphibole lamellae. The analytical water content due to the structural OH defect concentration of the light-green crystal part amounts to 0.0016wt.%, that of the colourless part is lowered by a factor of about 50. According to optical absorption spectra, the light-green colour of the crystal is essentially caused by an Fe2+–Fe3+ charge transfer. The relatively high concentration of OH defects in the light-green crystal part associated with higher Al contents relative to the colourless part suggests that OH is incorporated as hydrodiopside component, CaMg(SiAlO5OH). It is concluded that increasing water activity during the crystallisation process causes the formation of amphibole lamellae under consumption of nearly all of the water available in the fluid phase. It is further concluded that the observed hydrogen content of diopside represents a primary incorporation and not the result of late hydrothermal alteration processes.Received July 11, 2002; accepted October 30, 2002 Published online February 24, 2003  相似文献   

4.
Summary The Ni–Cu–Platinum Group Element (PGE) sulfide deposits of the Sudbury Structure have provided a major portion of the worlds total nickel production and their host rocks have been the subject of numerous research studies, yet a number of perplexing problems remain to be solved. On the one hand, studies seeking to explain the formation of the Sudbury Structure have now converged on a genetic model which proposes that the Main Mass and Offset Dykes of the Sudbury Igneous Complex (SIC) were produced by crystallization of an impact-generated melt sheet. On the other hand, these models have yet to be fully reconciled with the production of the very large volume of magmatic Ni, Cu, Co, and PGE-rich sulfide mineralization and the associated mafic rock types. This paper explores this problem using new precious metal data from the Main Mass and Offset Dykes. These data are used to understand the relationships between these rocks, and to provide constraints on how the Ni–Cu–PGE sulfide ore deposits fit into the geological evolution of the Sudbury Structure.In the two drill cores selected for study in this project, the Mafic Norite has 1–5 modal percent pyrrhotite plus chalcopyrite, and elevated Ni (40–1000ppm), Cu (40–1140ppm), and PGE (1.9–7.8ppb Pd, 1.8–7.3ppb Pt); this is overlain by Felsic Norite that contains pyrrhotite, and has a wide range in concentration of Ni (13–257ppm), Cu (7–328ppm), and PGE (<0.01–6.4ppb Pd, <0.01–5ppb Pt). For a similar range of MgO, the upper portion of the Felsic Norite unit has 5–10 times lower Ni and Cu abundances than within-plate basalts and local crustal rocks, and PGE abundance levels are mostly below analytical determination limits. Stratigraphic studies of other compositional profiles around the SIC demonstrate that this depletion signature of Ni, Cu, and PGE is widespread and developed not only above mineralized embayments and offsets, but also above barren sections of the lower contact of the SIC.The depletion of the upper part of the Felsic Norite in Ni, Cu and PGE is presumably due to equilibration of the magma with magmatic sulfide, and accumulation of this dense sulfide liquid. Results of modeling indicate that the parental magma giving rise to the Mafic and Felsic Norites had initial Ni and Cu contents of 210 and 110ppm, respectively. In addition, Ni, Cu and PGE tenors calculated in 100% sulfide from the Copper Cliff Offset average 13% Cu, 6% Ni, 18ppm Pd, and 19ppm Pt indicating that these sulfides had formed by fractionation from magmas that contained 310ppm Ni, 310ppm Cu, 18ppb Pd and 19ppb Pt. These values are factors of 3 to 5 higher than the Ni, Cu, Pd, and Pt contents of the Onaping Formation with average values of 55ppm Ni, 48ppm Cu, and 4.9ppb Pd as well as the marginal sulfide-poor phase of the Worthington Offset quartz diorite, which has average values of 61ppm Ni, 59ppm Cu, 2.8ppb Pd and 4.0ppb Pt. Both the Onaping Formation and the marginal quartz diorite are believed to represent the initial composition of a large component of the melt sheet. There is therefore a fundamental problem in reconciling the initial metal contents of the SIC magma as indicated by the marginal phases of the Offset dykes and that of the Onaping Formation with the composition of the SIC magma at the times of formation of the sulfides as indicated by their Ni, Cu and PGE tenors.It is proposed that because the SIC melt sheet was initially superheated with a temperature of 1700°C, it was able to dissolve 5 times as much S as it could at its liquidus temperature of 1200°C. It was also initially composed of an emulsion of mafic and felsic melts (Marsh and Zieg, 1999), which may have formed discrete magma cells. As the temperature of the melt sheet decreased, some of these magma cells became S-saturated and the resultant Ni–Cu–PGE sulfides settled downwards and on reaching magma cells lower in the melt sheet were re-dissolved thereby raising the Ni, Cu and PGE contents of the lower magma cells. It was from these enriched magma cells that precipitation of the ore-forming Ni–Cu–PGE sulfide melts eventually took place.The mineral potential of Offset and embayment structures appears to be empirically linked to the thickness of the overlying noritic rocks; for example, the most heavily mineralized embayments and Offset Dykes are located in areas where the Felsic Norite is thickest. It appears unlikely that the entire 1–3km-thick melt sheet was convectively mixing throughout its lateral extent, and so the heterogeneity in sulfide distribution was retained after crystallization and cooling.  相似文献   

5.
Summary High-grade gneisses from the Pulur complex in NE Turkey bear evidence for biotite-dehydration melting at 820°C and 0.7–0.8GPa, melt segregation and near-isothermal decompression to 0.4–0.5GPa. During further exhumation, the rocks underwent secondary pervasive rehydration at temperatures between 400 and 230°C and fluid pressures between 0.3 and 0.1GPa. Metamorphic peak conditions are dated at 331–327Ma, while hydrothermal retrogression occurred significantly later at 315–310Ma under static conditions. During the rehydration event, primary high-grade mineral assemblages including garnet, cordierite, sillimanite, spinel, biotite, plagioclase and ilmenite were extensively replaced by muscovite, paragonite, margarite, corundum, diaspore, chlorite, kaolinite, pumpellyite, prehnite, epidote, titanite, anatase, pyrite and chalcopyrite. Secondary mineral assemblages indicate that the infiltrating fluids were characterized by low fO2, very low XCO2 (<0.002), variable activities of Ca2+, K+, Na+ and H+ and relatively high activities of H2S and CH4. Quartz veins that might have acted as pathways for the fluids are rare. Ubiquitous veinlets consisting of (i) albite, (ii) chlorite+calcite+quartz or (iii) K-feldspar+calcite+quartz were formed after the pervasive rehydraton event by precipitation from aqueous solutions that were somewhat richer in CO2.  相似文献   

6.
Summary Geochronological data (U–Pb, Rb–Sr and 40Ar/39Ar) are used to unravel the Late Alpine high-grade metamorphism, migmatisation and exhumation of Variscan granitoids within the core of the Central Rhodopean dome, Bulgaria. The age of the granitoid protolith is 300±11Ma, as determined by U–Pb analyses on single zircons selected from the core of the dome structure.Rb–Sr whole rock data define an errorchron with a large scatter of the data points due to the Late Alpine metamorphic overprint. The slope of the reference line indicates a Variscan magmatic event. Strontium characteristics are used to discriminate the samples most influenced by metamorphism from those, which reflect possible differences in the protolith age of the granitoids.Petrological-geochemical data, the initial strontium ratio of 0.708±0.001, and Hf zircon values ranging from –2.58 to –3.82 point to a mixed, but crust-dominated origin of the Variscan magmas; young crustal material and mantle fragments were sources for the I-type metagranitoids.The exhumation of the granitoids from depths greater than 20–25km to about 5km below the surface was a rapid geological process. It started with the formation of granitic eutectic minimum melts at the temperature peak of metamorphism. Monazite crystallisation at about 650°C continued during isothermal decompression to possible depths of about 10–12km. An age of 35.83±0.40Ma was determined using conventional U–Pb isotope methods on four multigrain monazite fractions. A maximum average age of 36.6–37.5Ma (assuming same error uncertainties) for crystallisation of the metamorphic monazites was calculated assuming 10 to 20% monazite resetting during the subsequent Oligocene volcanism and hydrothermal activity in the region of the Central Rhodopean Dome. The rocks were then cooled to about 350–300°C at 35.35±0.22Ma according to 40Ar/39Ar ages of biotites and below 300°C at 35.31±0.25Ma (Rb–Sr data), as indicated by crystallisation of adularia in an open vein subsequent to pegmatite intrusion. A minimum exhumation rate of 3–5km per 1 million years can therefore be calculated for the exhumation of the metagranitoids during the period from 38–35Ma.  相似文献   

7.
Summary Geochemical data for 870 ore samples of 14 nickel sulphide (NiS) deposits from throughout the major Archaean Kambalda ore field, Western Australia, reveal highly heterogeneous Ni tenor (wt% Ni in 100wt% sulphide) variation that is difficult to explain solely by magmatic processes. The Ni tenor values for the deposits range from 6.2wt% Ni (Helmut deposit) to 19.7wt% Ni (Carnilya Hill deposit), close to the range for within single deposits (9.7–19.3wt% Ni). Contents of Ni and platinum-group elements (PGE) broadly increase with decreasing Fe and with increasing abundance of metamorphic pyrite+magnetite±silicates. In turn, the abundance of the metamorphic phases appears to be complexly related to structural setting, metamorphic grade, alteration type, and proximity to felsic intrusion. Chondrite-normalised multi-element plots of deposit compositions reveal relative depletions in Au, As, Bi, and Te.The relationship of increasing Ni content with secondary phase abundance indicates a strong role for metamorphic modification in the tenor variation. Replacement of pyrrhotite by pyrite+magnetite±chlorite during oxidation reduced the abundance of Fe sulphide relative to Ni sulphide and increased the Ni tenor of the residual sulphide. The extent of the oxidation reflects the extent of alteration fluid ingress along deformation structures and fabrics during talc-carbonate alteration, regional metamorphism, and felsic intrusion related to D3. The relative depletions of Au, As, Bi and Te combined with relative enrichments of these metals in nearby orogenic gold deposits mean that NiS deposits could represent metal reservoirs for Archaean gold hydrothermal systems.  相似文献   

8.
Summary In this paper we present what is, to the best of our knowledge, the first comprehensive study of clinopyroxenes and plagioclases contained in the flows of the Grande Ronde Basalt member of the Columbia River Basalt Group (northwestern USA). The rocks have MgO(wt%)<6%, and trace amounts of Cr and Ni. About 56% of extracted solid containing normative clinopyroxene and plagioclase explains the liquid line of descent from the more mafic sample (MgO wt%=5.89) to the most evolved. The most ubiquitous phases in the basalts are plagioclase and augite. Ilmenite and magnetite are accessories in all rocks. Olivine is present in small amount only in one sample (RT 89-7). Based on principles of Ca–Na plagioclase–liquid exchange, estimates of pre-eruptive magmatic water are < 2.4wt%. From clinopyroxene–liquid equilibria, calculated pressures and temperatures of ascending magmas are between 1atm and 0.617GPa, and 1068°C and 1166°C, respectively. Compositions of magnetite–ilmenite pairs and olivine–clinopyroxene–oxide assemblages yield post-eruptive oxygen fugacities of NNO=–1.923, and one pre-eruptive value of NNO=– 2.455. A simple model of asthenospheric melting and magma ponding in the lower crust fits the physical parameters.Supplementary material to this paper is available in electronic form at http://dx.doi.org/10.1007/s00710-003-0017-1  相似文献   

9.
Summary On Diego de Almagro Island in Chilean Patagonia (51°30S), a convergent strike slip zone, the Seno Arcabuz shear zone, separates the Diego de Almagro Metamorphic Complex from very low grade metagreywackes in the east, which were intruded by Jurassic granitoids. The Diego de Almagro Metamorphic Complex is composed of a metapsammopelitic sequence containing blueschist intercalations in the west and (garnet) amphibolite lenses in the east. Peak metamorphic conditions (stage I) at 9.5–13.5kbar, 380–450°C in the blueschist and at 11.2–13.2, 460–565°C in the amphibolite indicate subduction and accretion at different positions within the deepest part of the accretionary wedge. A K–Ar age of 117±28Ma of amphibole approximately dates the peak of metamorphism in the amphibolite. The early retrograde stage of metamorphism occurred under static conditions and resulted in localized equilibration (stage II) at 6.3–9.6kbar, 320–385°C in the blueschist and 6.1–8.4kbar, 310–504°C in the amphibolite. Both P-T paths converge within a midcrustal level.In contrast, an orthogneiss of trondhjemitic composition occurring within the Seno Arcabuz shear zone is associated with a garnet mica-schist containing a high temperature/intermediate pressure assemblage formed at 4.9–6.5kbar, 580–690°C. A muscovite K–Ar age of 122.2±4.6Ma dates cooling after this event which is related to a concomitant magmatic arc. These rocks were overprinted by a mylonitic deformation, which is caused by convergent strike slip shearing and ends during formation of a retrograde phengite-chlorite-stilpnomelane assemblage at a minimum pressure of approximately 5.7kbar (at 300°C).Zircon fission track ages from rocks of the Seno Arcabuz shear zone are 64.9±2.7 and 64.9±2.7Ma; they record the end of shearing in the Seno Arcabuz shear zone that juxtaposed all rocks in the middle crust. Zircon fission track ages ranging from 78 to 105Ma in the South Patagonian batholith to the east indicate earlier cooling through 280°C. The rocks of the Diego de Almagro Metamorphic Complex were initially slowly exhumed and resided at a midcrustal level before being emplaced via shearing in the Seno Arcabuz shear zone. Apatite fission track ages (54±8Ma) from the Seno Arcabuz shear zone show that exhumation and cooling rates increased after this event. The incorporation of continental crust within the subduction system was a late process, which modified the Cretaceous accretionary wedge, resulting in considerable shortening of the convergent margin.  相似文献   

10.
Summary The provenance of the Mid-Devonian clastic sediments in the Teplá-Barrandian Unit (TBU) of the Bohemian Massif was investigated by laser ablation ICP-MS U–Pb zircon dating, bulk sediment geochemistry and mineralogical study of the heavy mineral fraction. In contrast to the island arc provenance of the TBU Neoproterozoic sediments, the Early Palaeozoic sediments contain significant amounts of differentiated crustal material. The detrital zircon populations in the Barrandian Mid-Devonian siltstones and sandstones show ages ranging from Archaean (3.0Ga) to Early Palaeozoic (0.39Ga). Major age maxima are at 2.6Ga, 2.0–2.25Ga, 0.62 and 0.51Ga. The youngest identified zircons so far correspond to Lower and Mid-Devonian ages. The extensive mechanical abrasion of zircons having Archaean (3.0, 2.8 and 2.6Ga) to Paleoproterozoic ages (2.25–2.0Ga) suggest their provenance from recycled old sedimentary sequences. The relatively large number of zircons with ages between 2.0 and 3.0Ga may indicate the presence of relicts of the Archaean/Paleoproterozoic crust in the source areas of the studied Mid-Devonian sediments. The absence of detrital zircon ages between 0.9 and 1.2Ga and the presence of zircon ages of 2.0–2.25 and 0.5–0.8Ga correspond to the zircon age pattern from the Gondwana-related North African, rather than Gondwana-related South American and Baltic terranes. The material was entering the basin predominantly from the west and consisted primarily of detrital material of Cambrian granitoids and recycled material of Neoproterozoic meta-sedimentary sequences.  相似文献   

11.
Summary Titanite varieties doped with rare earth elements (REE) have been prepared by ceramic synthesis and quenching in air. Their crystal structure was determined by Rietveld analysis of the powder X-ray diffraction patterns. Two different substitution schemes, Ca1–xNax/2Smx/2TiSiO5 and Ca1–xDyxTi1–x SiO5, are studied at x=0.2. Both synthetic varieties of titanite adopt space group A2/a. This implies that both single-site and complex multivalent substitutional schemes destroy the coherence of the off-centering of octahedral chains in the titanite structure resulting in a P21/aA2/a phase transition. Unit cell dimensions obtained for the REE-bearing titanite varieties are as follows: a=7.0541(1)Å; b=8.7247(1)Å; c=6.5664(1)Å; =113.732(1)° for Ca0.8Na0.1Sm0.1TiSiO5; and a=7.0021(1)Å; b=8.7256(1)Å; c=6.5427(1)Å; =113.294(1)° for . Both REE-doped titanite samples and a control sample of the pure titanite end member have similar unit cell parameters and consist of polyhedra distorted to a similar extent with the exception of more-distorted SiO4 tetrahedron in CaSiTiO5. The structural data suggest that the Ca1–xNax/2Smx/2TiSiO5 and Ca1–xDyxTi1–xFexSiO5 solid solutions adopting the titanite structure might extend to x sufficiently greater than 0.2 and involve both heavier and lighter trivalent rare earth elements.Permanent address: Geological Institute KSC RAS, 14 Fersmana St., Apatity, 184200 Russia  相似文献   

12.
Summary ¶This study experimentally investigated the transformation kinetics of synthetic polycrystalline aragonite to calcite at four temperature/pressure conditions (330°C/200MPa, 380°C/325MPa, 430°C/580MPa, and 480°C/875MPa), close to the calcite-aragonite equilibrium phase boundary. The extents of transformation measured as a function of time in a synthetic system, using in-situ annealed, high purity samples, are consistent with the kinetic model for grain-boundary nucleation and interface-controlled growth. The growth rates are slightly lower than those previously determined for a natural polycrystalline sample at 330 and 380°C. The activation energy (158kJ/mol) for calcite growth from synthetic samples is lower than that (247kJ/mol) from natural samples, but is close to the previously reported value (163kJ/mol) from a single crystal aragonite. The extrapolation of our experimental data to natural conditions reveals unusually fast transformation rates, in contrast to those of natural samples. The presence of deformational strain, fractures, defects or impurities in natural samples, and other factors may account for the discrepancy. This study suggests that the retrograde metamorphism of aragonite to calcite may proceed in a wide range of rates also depending on other geological factors than temperature and pressure.Received July 15, 2002; revised version accepted May 15, 2003  相似文献   

13.
Summary A fully cored drillhole was drilled to 1596m by the Czech Geological Survey in 1961–1963 in the central part of the Cínovec (Zinnwald) granite cupola. Two types of granite were intersected: zinnwaldite granite (ZG), observed down to a depth of 730m, and protolithionite granite (PG), occurring to the end of the hole. The core was used to study the distribution and chemistry of: zircon, thorite, xenotime, monazite, bastnäsite, synchysite, REE oxyfluorides and hydroxyfluorides. Zircon occurs throughout the drillcore; it is strongly hydrated and fluorinated with about 18.5wt.% H2O content in the apical part of the cupola. Its F-content reaches 2.41wt.%. Within the PG, the F concentration in zircon is low. Zircon is poor in Th and U and its HfO2 contents vary from 1.01 to 5.24wt.%. Thorite is common in the PG, becoming rare in the ZG. It is strongly hydrated (up to 14wt.% H2O) and fluorinated (up to 2.04wt.% F). Extensive solid solution between ThSiO4 and YPO4 was observed. Xenotime is strongly hydrated (up to 16wt.% H2O), but its F content is low (<0.31wt.%). Two types of monazite were identified: Th-rich (up to 9.3wt.% ThO2) in the ZG, and Th-poor (<2.5wt.% ThO2) in the PG. Monazite remained stable during the hydration and fluorination process. Its REE chondrite-normalized distribution patterns show negative anomalies for La and Nd and a pronounced negative anomaly for Eu. Chemical compositions of several REE oxyfluorides and hydroxyfluorides were studied. REE fluorocarbonates are represented by bastnäsite and synchysite. Bastnäsite is abundant in the ZG. Its chondrite-normalized REE patterns are characterized by an important negative Eu anomaly and downward kinks at La and Nd. Synchysite-(Ce) and synchysite-(Y) are particularly well developed in the deeper parts of the cupola, and exhibit REE distribution patterns characterized by a weak negative Eu anomaly (synchysite-(Ce)), or a weak positive Eu anomaly (synchysite-(Y)).The distribution of accessory minerals reveals five major evolution stages: (1) Early magmatic crystallization of albite and orthoclase. (2) A late magmatic stage comprising protolithionite, quartz, accessory zircon, thorite, xenotime and monazite. (3) Interaction of this magmatic association with a fluid phase rich in F, CO2 and H2O, leading to the transformation protolithionite zinnwaldite and to the remobilisation of Nb, Ta, Ti, W, Sn. Accessory minerals formed during stage (2) were hydrated and fluorinated, except monazite. (4) The transfer of volatiles into the apical part of the cupola followed by the opening of the magmatic system generated microgranites and hydrolysis-type reactions leading to the appearance of REE oxyfluorides and hydroxyfluorides. (5) A late CO2- and F-rich fluid phase was responsible for the deposition of REE fluorocarbonates. Monazite and xenotime became unstable in the apical part of the cupola. An influx of fluids with high Ca-activity occurred late during stage (5) and led to the formation of synchysite, and finally to the extensive precipitation of fluorite.  相似文献   

14.
Summary The investigated Al-phosphate- and Al-borosilicate-bearing metaquartzite horizon belongs to the Middle Proterozoic Serra de Vereda member of the São Marcos Formation of the northern Espinhaço fold belt. Outcrops are located in the NNW–SSE trending hills of the Serra de Canas/Cana Brava (Northern Serra do Espinhaço, State of Bahia, NE Brazil) about 10km west of the town of Boquira. Sky blue lazulite and deep blue to lilac dumortierite are enriched in layers which sometimes show relic cross bedding. The occurrence of hematite patches and layers is typical. In rocks of type A, phosphorus contents range from 1.89wt.% to 10.73wt.% P2O5 and boron contents are mostly below 10ppm whereas in the rocks of type B phosphorus contents are below 1% and boron contents reach 2600ppm with a mean value of 1139ppm. REE distribution patterns of rocks are predominantly controlled by the amount of xenotime, monazite and zircon. Oxygen thermometry on quartz and hematite and the stability of kyanite, augelite, trolleite and berlinite allow to estimate the minimum metamorphic peak P-T conditions at 475°C and 3.8kbar i.e. within the stability field of scorzalite–lazulite and dumortierite. The association of Al-phosphates with hematite layers provides evidence for the deposition of the metaquartzite protolith in a seawater-fed sabkha-like sand flat fringing the Espinhaço rift. It is proposed that apatite, Al-phosphates and Al-borosilicates were chemically precipitated together with iron hydroxides from pore fluids. The antithetic behaviour of phosphorus and boron contents in the metaquartzites is the consequence of an influx of toxic boron-rich water that drastically affected algae populations and consequently reduced phosphorus precipitation.  相似文献   

15.
Summary In-situ analyses of boron using secondary ion mass spectrometry (SIMS) is impeded by surface contamination of the analysed samples. We analysed 40 different natural and synthetic silicate materials, including meteoritic and mantle minerals, in order to find a material with an extremely low boron content that allows us to quantify the level of contamination. Different cleaning procedures were tested, and it was shown that using an ultrasonic cleaner with ultrapure water to clean the sample and setting the imaged field of the ion probe smaller than the primary beam spot reduces the boron contamination level to <2ng/g at a total analysis time of 12min (pre-sputtering: 400s).Herasil 102, a pure synthetic SiO2 glass manufactured by Heraeus Quarzglas GmbH, Germany, was found to contain 1ng/g boron, and therefore we recommend this glass as a sample to test the contamination level of boron in SIMS analyses.Results for lithium show that analysis of this element is also influenced by contamination, but the contamination levels are much lower than those for boron.  相似文献   

16.
The axial base and skin capacities of piles bored in cohesion less soils are often estimated using empirical, semi-empirical and theoretical methods. The aim of this paper is to assess the applicability and evaluate the accuracy of different predictions methods available in the literature, via comparison with data from 43 field pile load tests conducted on shafts drilled in the region of the United Arab Emirates. Janbu's theoretical method (1989) with the parameter (=75°) and Vesics theoretical method (1975) yielded accurate predictions for the base resistances. Burlands approach (1973) overpredicts the skin capacities with an average predicted-to-estimated ratio (q p /q e) of three times greater than the unity while using values of the coefficient of earth pressure (k=05k o ) and the angle of soil-pile friction (=23).  相似文献   

17.
Summary Abyssal tholeiite is generated by partial melting of the upper mantle. The mantle sections of ophiolite complexes show that partial melting leaves mantle residua that are lherzolitic or harzburgitic, harzburgite being the more depleted residuum. It is shown that some of the interstitial melt of partially molten harzburgite approximates a tholeiitic composition. Therefore, the solidus of harzburgite constitutes the maximum possible temperature for the generation of primary tholeiite. The MgO contents of primary tholeiites in equilibrium with harzburgite are determined to be about 21 and 23wt.% MgO at 2.0 and 3.0GPa, respectively. The possible MgO contents of primary abyssal tholeiite is suggested to range between 10 and 23wt.% MgO, with the MgO content increasing with increasing pressure.  相似文献   

18.
Summary Metamorphosed carbonatites and related skarn deposits, located in Fuerteventura Basal Complex, contain unusual Sr-rich minerals. Maximum SrO concentration in the following minerals are: calcite, 7.23wt%; apatite, 5.22wt%; epidote, 11.64wt%; clinozoisite, 1.25wt%; allanite, 5.63wt%; britholite, 4.11wt% and a Sr–Na aluminosilicate (probably stronalsite), 16.44wt% SrO. Calcite and apatite are chemically similar to those found in carbonatites and are therefore considered to be of igneous origin. Textural evidence indicates that the first skarn stage garnet+diopside+Sr–Na aluminosilicate formed as the result of chemical interaction between carbonatites and adjacent silicate rocks. The formation of Sr-bearing epidote/clinozoisite, allanite and britholite appears to be related to the release of Sr into the fluid phase from the breakdown of high temperature assemblages during the retrograde skarn stage. During the final evolution stages, further alteration of britholite by bastnäsite and törnebohmite took place. The occurrence of REE minerals shows that the fluids responsible for this metasomatism must also have transported significant quantities of REE.  相似文献   

19.
Summary ¶The crustal structure of the Campania continental margin is synthesized from outcrop, seismic reflection and gravimetric data. Outcrop and subsurface geological data reveal the presence of NE–SW faults, E–W faults and NW–SE faults. An older extensional event occurred along NW–SE faults and was followed by the main extensional event linked to the activity of NE–SW normal faults. The latter were active between 700 and 400ka producing half-grabens filled by more than 5km of Quaternary deposits. The stratigraphic signature of these tectonic events corresponds to a Lower Pleistocene marine unconformity-bounded unit overlain by Middle Pleistocene rocks belonging to a transgressive-regressive cycle. A crustal section of the Campania margin displays an asymmetric linked fault system characterized by a 10–12km-deep main detachment level, listric normal faults and rollover anticlines. Structural and stratigraphic data document that the inception of volcanic activity at Vesuvius occurred at 400ka, just after the main extensional event, and the volcano is located at the margin of a rollover anticline.Received June 26, 2002; revised version accepted November 9, 2002  相似文献   

20.
Zusammenfassung Die in Entstehung befindliche hydrothermal-sedimentäre Lagerstätte Atlantis-II-Tief im Roten Meer wurde in den Jahren 1969, 1971 und 1972 von den Forschungsschiffen Wando River und Valdivia aus genauer untersucht. Die Detailkartierung zeigt eine Fallenstruktur, die hauptsächlich durch NW-streichende Grabenrandverwerfungen hervorgerufen wurde. Die in die se Depression in ihren tiefsten Teil einströmenden metallhaltigen Solen hielten das für die Lagerstättenbildung, besonders das für die Sulfidausfällung nötige Milieu über längere Zeit aufrecht. Diese seit dem ausgehenden Pleistozän anhaltende stabile Situation wurde einige Male von Lava-Ausflüssen, tektonischen Ereignissen und Verlagerung der Quellen unterbrochen. Diese Vorgänge und die komplizierte Morphologie der solegefüllten Becken führten zu einer sehr komplexen Faziesentwicklung und stratigraphischen Abfolge. Insgesamt läßt sich, von den Quellen ausgehend, eine Zonierung von sulfidisch-silikatischer zu manganitischlimonitischer Ausfällung beobachten.
The Atlantis II Deep, a hydrothermal-sedimentary metal depositin statu nascendi has been investigated in detail 1969, 1971 and 1972 with the research vessels Wando River and Valdivia. The new bathymetric map reveals a trap structure mainly caused by NW-striking faults, limiting local grabens. The metalliferous brines discharging into the deepest part of this depression maintained the conditions necessary for the formation of the deposit, esp. of the sulfides, for a long time.This stabil situation active since the end of the Pleistocene was several times disturbed by lava flows, tectonic events and displacement of the discharge vents.These events and the complicate morphologic structure of the brine-filled deep are responsible for a very complex development of lithologic facies and the stratigraphic sequence. There is a general deposit differentiation from sulfidic-silicatic precipitation near the discharge points and formation of limonite and manganite outside the brines.
Résumé Pendant les années 1969, 1971 et 1972 les gisements hydrothermaux sédimentaires Atlantis II, en voie de formation dans la Mer Rouge, ont fait l'objet de campagnes scientifiques détaillées entreprises par les navires océanographiques Wando River et Valdivia.La carte morphologique montre une structure de descente qui a été formée principalement par des failles de direction NW délimitant des graben. Les saumures métallifères affluant dans la partie la plus profonde de cette dépression ont maintenu pendant une certaine durée le milieu nécessaire à la formation du gisement, et surtout à la précipitation des sulfures. Cette situation restée stable depuis la fin du Pléistocène a été interrompue plusieurs fois des émissions basaltiques, par des dislocations tectoniques et par le déplacement des sources. Ces événements, ainsi que la morphologie compliquée du bassin rempli de saumures, ont conduit à un développement très complexe des faciès lithologiques et de la séquence stratigraphique. Dans l'ensemble on peut constater une zonation des faciès avec précipitations sulfurosilicatées près des points d'entrée des saumures et manganolimonitiques plus à l'écart.
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