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1.
Minerals of the triphylite-lithiophilite, Li(Fe, Mn)PO4, and the triplite-zwieselite-magniotriplite series, (Mn, Fe, Mg)2PO4F, occur in the late stage period of pegmatite evolution. Unfortunately, neither are the genetic relationships between these phosphates fully understood nor are thermodynamic data known. Consequently, phosphate associations and assemblages from 8 granitic pegmatites — Clementine II, Rubicon II and III, and Tsaobismund (Namibia); Hagendorf-Süd and Rabenstein (Germany); Valmy (France); Viitaniemi (Finland) — have been tested for compositional zoning and intercrystalline partitioning of main elements by electron microprobe techniques. Although the selected pegmatites display varying degrees of fractionation, and the intergrowth textures indicate different genetic relationships between the phosphates, the plots of mole fractions X Fe=Fe/(Fe+Mn+Mg+Ca), X Mn=Mn/(Fe+Mn+Mg+Ca), and X Mg=Mg/(Fe+Mn+Mg+Ca) can be fitted relatively well with smooth curves in Roozeboom diagrams. Their deviations from symmetrical distribution curves are mainly dependent upon X Mg or X Ca, and upon non-ideal solutions. Surprisingly small differences between the partition coefficients were detected for intergrowths of different origin. However, the partitioning of shared components among coexisting phases is clearly dependent upon the conditions of formation. Compositional zoning is observed only when both Fe–Mn phosphates are intergrown mutually or with other Fe–Mn–Mg mineral solid-solutios. Thus, the zoning does not seem to be due to continuous crystallization, but to later diffusion processes. The triplite structure has preference for Mn, Mg, and Ca, while Fe prefers minerals of the triphylite series. A quantification of main element fractionation between minerals of the triphylite and the triplite series is possible in the cases where diffusion can be excluded. For the Fe/(Fe+Mn) ratios of core compositions an equation with a high correlation coefficient (R=0.988) was determined: Fe/(Fe+Mn)Tr=[Fe/(Fe+Mn)Li]/{2.737-(1.737)[Fe/(Fe+Mn)Li]} (Tr=triplite series, Li=triphylite series). Consequently, the Fe/(Fe+Mn) ratio of the triplite series can now also be used in the interpretation of pegmatite evolution, just like that of the triphylite series which has been successfully applied in the past.  相似文献   

2.
New occurrences of the phosphates sarcopside/graftonite (Fe, Mn)3(PO4)2, farringtonite (Mg, Fe)3(PO4)2, and brianite Na2CaMg(PO4)2 in iron meteorites are reported. The sarcopside in Duel Hill (1854) (IVA-Anom) contains less than 0.1 mole % Mn3(PO4)2 and more nearly approaches the Fe-rich end member than does any previously reported natural occurrence. This identification of farringtonite in Barranca Bianca (IIE) is the first report of this mineral in a meteorite group other than the pallasites.  相似文献   

3.
Zusammenfassung Die C12/C13-Verhältnisse des Karbonatanteils metamorpher Gesteine liegen mit ihren C13-Werten zwischen –8,2 und –22,9 recht niedrig. Die Graphitanteile haben ein C-Isotopenverhältnis –15,7. Prä- bis postkambrischer Marmor aus verschiedenen europäischen Vorkommen ist auf Grund der Isotopenrelationen des Karbonatkohlenstoffs vermutlich marin entstanden. Seine Graphite lassen sich in 2 Gruppen einteilen: Gruppe I mit –19,4 bis –28%.; Gruppe II mit –5,2 bis –16,8. Die S32/S34-Verhältnisse von sulfidischem Eisenerz aus eklogitischen Gesteinen der Münchberger Gneismasse haben einen relativ kleinen Schwankungsbereich, von 12,0.
The C12/C13-ratio of carbonate-carbon in metamorphic rocks is relatively low: C13: –8,2 to –22,9; graphitic carbon shows its normal isotopic composition: –15,7. Pre- and postcambrian marbles can be presumed of marine origin on the ground of the isotopic composition of carbonate-carbon whereas their graphites can be divided in two groups: Group I has a C12/C13-ratio supposed to be typical of organic origin; Group II is surprisingly high in C13. The S32/S34-ratios of ironsulfides from eclogitic rocks (Münchberger Gneismasse) show a relatively narrow spread of 12,0 per mil.
Résumé Le rapport C12/C13 du carbone des carbonates dans les roches métamorphiques est relativement petit (C13 =–8,2 à –22,9). Le carbone graphitique a sa composition isotopique normale, – 15,7. Les marbres pré- à postcambriens sont probablement marins selon la composition isotopique des carbonates. Leurs graphites forment deux groupes: le premier groupe a des rapports C12/C13 typiques d'une origine organique, le deuxième groupe contient plus de C13 que la normale. Les relations S32/S34 des sulfures de fer des roches éclogitiques (Münchberger Gneismasse) ne montrent pas de grandes variations isotopiques (12,0).
12/13 , . . 13 8,2 22,9 . 15,7 . , , , . : 19,4 28, — 5,2 16,8. S32/S34 , , 12,0.
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4.
Zusammenfassung Die Ophiolithe des Nordapennins werden nach ihrem Alter in verschiedene Gruppen eingeteilt. Nur im Gebiet nördlich von Genua und längs des Küstenstreifens zwischen Sestri Levante und Levanto läßt sich die alte Anschauung eines oberjurassischen bis tief unterkretazischen Alters der Ophiolithe rechtfertigen. In dem noch verbleibenden Gebiet konnte für einzelne Vorkommen ein wesentlich jüngeres Alter (O.-Alb bis U.-Turon) wahrscheinlich gemacht werden. Von Bedeutung für diese Alterseinstufungen waren die fast alle Ophiolithvorkommen begleitenden Brekzien, die in einzelnen Typen untergliedert und beschrieben werden.
Northern Apennitie Ophiolites are subdivided by their age. North of Genoa and along the coast between Sestri Levante and Levanto only, the rocks are Upper Jurassic or Lowest Cretaceous of age; the remaining area shows an Upper Albian to Lower Turonian age of ophiolithes.
Résumé Les ophiolites des Apennins septentrionaux sont, suivant leur âge, subdivisés en différents groupes. C'est seulement dans la région au Nord de Gênes et le long de la bande côtière entre Sestri Levante et Levanto que se vérifie pour les ophiolites l'ancienne conception d'un âge allant du Jurassique supérieur à la base du Crétacé inférieur. Dans le territoire restant on peut attribuer à certains affleurements un âge notablement plus récent (Albien supérieur jusqu'au Turonvien inférieur). Pour fixer cet âge, on s'est appuyé sur les brèches qui accompagnent la plupart des ophiolites; ces brèches ont été décrites et subdivisées en quelques types.
Riassunto Le ofioliti dell'Appennino Settentrionale si suddividono in due gruppi secondo la loro età. Solo per la zone Nord di Genova e la striscia costiera tra Sestri L. é Levanto vale la vecchia opinione sull'età supragiurassica-infracretacea delle ofioliti. Nelle altre parti dell'Appennino si può attribuire a certi affioramenti con molta probabilità un'età molto più recente (Albiano Sup. - Turoniano inf.). Di grande importanza per una tale datazione si dimostrarono le brecce, per lo più sedimentarie, che circondano quasi tutte le masse ofiolitiche e che si intercalano a sedimenti fossiliferi o ne contengono frammenti. Vengono descritti alcuni tipi litologici di queste brecce.
. - , . .
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5.
The distribution of some trace metals (Cu, Zn, Ni, Co,Fe, Mn) and of DOC over a particulate (> 1 m),a colloidal (size < 0.45 m and molecular weight > 10 kD) and an ultrafiltered fraction (< 10 kD)was determined at several sites on the Thur River,Switzerland, at various times of the year. Thecomplexation of Cu by strong ligands in theultrafiltrate and in the conventional filtrate (<0.45 m) was compared using a ligand-exchange/CSV method.The <0.45 m concentrations of Cu (from anaverage of 7 nM to 24 nM), Zn (<5–23 nM), Ni (5–13 nM),Co (1.5–3 nM) and Mn (7–92 nM)increased downstream. The major part of Cu, Zn, Niand Co usually occurred in the ultrafiltratefraction at all sites, whereas Fe and Mn were mostlyin the particulate fraction, under conditions of lowsuspended matter content (< 10 mg L-1) in theriver. The percentage of metal in the colloidalfraction, with respect to the 0.45-m filtrate,decreased in the order: Cu (median 11%) > Zn Ni(median 5–6%) > Mn Co (median < 5%). DOCalso consisted mostly of molecules in the < 10 kDrange.Cu was strongly complexed by natural organic ligandsin all filtrate and ultrafiltrate samples. A largepart of the strong Cu binding ligands consisted ofcompounds in the < 10 kD range, but colloidalligands with similar properties also occurred. Cu wasdistributed among the dissolved and the colloidalligands, roughly in proportion to organic carbon.The colloidal fraction (as defined here) did notincrease in its proportional amount downstream and wasonly of limited significance in transporting traceelements in the Thur River under low discharge conditions.  相似文献   

6.
Ninety-seven mineral phases consisting of ten chloritoids, fifteen epidotes, sixteen garnets, four sphenes, seven rutiles, seven pyroxenes, thirteen blue amphiboles, two green amphiboles, eleven phengites, two paragonites, a mariposite, seven chlorites, and two specimens of albite were obtained from the metamorphic rocks of Île de Groix, and their chemical, physical, optical and X-ray properties determined. The chloritoids are all optically positive, monoclinic polymorphs with large 2V, moderate refractive indices and characterized by high densities. Their fluorine contents have been used to propose a new upper limit for OHF substitution in the chloritoid structure, suggesting that partial pressure of fluorine might modify the stability of chloritoids from that determined in pure H2O. The epidotes belong to the Al-Fe epidote series and are epidote sensu stricto. The almandine-rich garnets and the chloromelanites are metastable relics in the glaucophane schists. The grossular contents of the calcareous schist garnets are believed to have become depressed under high CO2 pressure and the low Tschermak's contents of the pyroxenes are to be explained by equilibria involving epidote at high and low temperature when the Tschermak's components will break down to epidote group minerals. The sphenes contain appreciable amounts of combined water, fluorine substituting for oxygen and aluminium substituting for silicon and titanium. The presence of H3O+ is suspected in a specimen of blue amphibole. The barroisite has a composition between glaucophane and hornblende. On account of its high Fe3+ content it is believed to have formed under higher P O 2 than the blue amphiboles. The paragonites which occur in the ohloritoid veins are unstable in the potassium-rich aluminous schists. The phengites show a tendency towards sericitic composition due to post-glaucophanisation readjustments under the lower pressure conditions of the greenschist facies. Some of the Fe3+ contents of the chlorites are interpreted as due to oxidation of ferrous iron, e.g. 2 [Fe(OH)2]2FeOOH + H2. The minerals show strong chemical control of the host rock and their Mn contents are directly related to those of the minerals from which they have evolved through retrogression.Chloritoids and epidotes that are not associated with garnets contain higher amounts of manganese; similarly, the two blue amphiboles with the highest FeMg ratios were obtained from rocks in which garnet has not appeared. It is therefore believed that ottrelite and piemontite would be stable only at the lowest subfacies of the greenschist facies. Also, the ironrich amphiboles must have evolved from low-grade iron-aluminium chlorites, since on the appearance of garnet in a schist iron-aluminium chlorites react with quartz to give almandine and Mg-rich chlorites. The Fe2+Mg ratios of the blue amphiboles therefore reflect the grade of the original schist in which the minerals formed.  相似文献   

7.
Meta-graywacke and meta-argillite of Archean age near Yellowknife contain biotite, cordierite, gedrite and sillimanite isograds towards the Sparrow Lake granite pluton. The chemistry of biotite, cordierite, gedrite and garnet in rocks that up-grade from the cordierite isograd indicate a small range of chemical composition, particularly with reference to Mg, Fe and Mn. The analyses show further that among the coexisting ferromagnesian minerals Fe/Fe+ Mg ratio decreases in the sequence: garnet, gedrite, biotite, cordierite while Mn/Fe+Mg+Mn ratio decreases in the sequence garnet, gedrite, cordierite, biotite. The same order is also observed in the distribution diagrams. The regular distribution of Mg, Fe and Mn among the coexisting phases demonstrate that chemical equilibrium was attained and preserved in these Archean rocks. Mg-Fe distribution between cordierite and biotite appears to be dependent on the temperature of crystallization or metamorphic grade.  相似文献   

8.
Zusammenfassung Der Vergleich der Gitterkonstanten und der Atomparameter von Amblygonit LiAI[PO4](OH,F), Kieserit Mg[SO4](H2O) und Titanit CaTi[SiO4](O) zeigt, daß diese Strukturen analog gebaut sind. Das Geriist von tetraedrischen und oktaedrischen Koordinationspolyedern ist in allen 3 Fallen gleich. Die Grundstruktur ist die des Kieserits. Die Amblygonitstruktur entsteht aus ihr durch Verzerrung und Auffüllung mit einem weiteren Bauelement, dem Li, die Titanitstruktur nur durch Auffullung ohne Symmetrieverminderung.  相似文献   

9.
The natural early-diagenetic environment ``anoxicporewater – authigenic mineral phases' has beencharacterized in sediment of the Gotland Deep,Baltic Sea, by a closed-system model. Occurrence ofcarbonate precipitates as thin almost pure whitelaminae was considered as a natural experiment forlong-term equilibration between these phases andporewater. Plots of distribution coefficientsindicate that metastable equilibrium exists betweenporewater and the authigenic Ca-rich rhodochrositephases below 7 cm depth. A thermodynamic model ofporewater geochemistry at in situ P = 25 barand T = 5 °C was developed using the Gibbsenergy minimization (GEM) approach. The values of isobaric-isothermal potentials of Mn, Ca, Fe, Mg,Sr, Ba, C, and O, calculated from the porewatercomposition, were used in a new ``dual thermodynamic'calculation approach to estimate solid activitycoefficients of the end-members in the non-idealsolid solution (Mn, Ca, Mg, Sr, Ba, Fe)CO3,i.e., at full major and minor multi-componentcomplexity. The regular Margules interactionparameters for the composing binaries estimated bythis model were Mn-Ca = 1.9 ± 0.5,Mn-Mg = 0.6,Ca-Mg = 3.7,Mn-Fe = 0.2,Ca-Fe = 2.8,Mn-Sr = 9.7,Ca-Sr = 2.15,Mn-Ba = 4.0,Ca-Ba = 1.4,validating the theoretical predictions given byLippmann in his pioneering 1980's paper. Thestrictly thermodynamic equilibrium model is not onlyable to match both the measured porewater andcarbonate solid-solution composition, but also topredict that the porewater pH, pe, alkalinity, anddissolved Mn, Fe, and S concentrations arecontrolled by the authigenic mineral bufferingassemblage mackinawite-greigite-rhodochrosite. Ourmodel is only compatible with the idea of ACRformation with typical composition (XMnbetween 70–75%) in the topmost sediment layerwhich, however, needs a major source ofMnaq II. This is provided by reduction ofparticulate Mn oxides precipitated in significantamounts in the water column upon major inflow eventsin the Baltic Sea. The model enables also to set upscenarios of changing environmental conditions, e.g.,to predict the non-linear response of the carbonatesolid-solution composition to changes in Mn loading,alkalinity and salinity of the sediment-watersystem. The results suggest that the major andespecially minor element contents (Sr, Mg, Ba) inauthigenic carbonates can be applied as anenvironmental paleoproxy.  相似文献   

10.
Zusammenfassung Schichtgebundene Mn-Anreicherungen sind in den Nördlichen Kalkalpen nahezu ausschließlich auf feinschichtige Tonmergelsteine (Manganschiefer) des oberen Toarcian und unter-bis mitteljurassische Rotkalke beschränkt.Die primären Mn-Minerale in der Manganschiefer-Fazies sind Mischkarbonate der Reihe CaCO3–MnCO3–FeCO3 und geringe Mengen von Braunit und Pyrolusit. Die Fe-Mineralisation charakterisiert eine Faziesreihe, die von schwach oxidierenden Ablagerungsbedingungen (Goethit, Hämatit) an der Basis der Mn-führenden Serie, zu reduzierenden (Siderit, Chamosit, Pyrit) führt. In den Rotkalken sind Pyrolusit und Goethit bzw. Hämatit in calcitreichen Knollen und Krusten konzentriert.Die chemische Zusammensetzung der Mn-reichen Gesteine ist bei hohen Ca- und SiO2-Gehalten von korrelierbaren Mn- und Fe-Anteilen in gleicher Größenordnung bestimmt. Gegenüber der durchschnittlichen Zusammensetzung faziell vergleichbarer Schwarz- und Tonschiefer und marin-sedimentärer Mn-bzw. Fe-Lagerstätten sind auch die Spurenelement-Gehalte deutlich erhöht und zumindest im Falle des Co mit den Mn-Gehalten korreliert.Nach ihrer mineralogischen und chemischen Zusammensetzung sind die Manganschiefer zu den vulkanogen-sedimentären Lagerstätten zu rechnen. Unmittelbare Hinweise auf vulkanische Aktivität im oberen Lias sind in Form von Seladonit-führenden Tuffen, die mit Mn-Karbonaten wechsellagern, erstmals in den Nördlichen Kalkalpen aufgefunden worden.
Distribution and genetic significance of jurassic manganese deposits in the Northern Limestone Alps
Summary In the Northern Limestone Alps strata-bound deposits of manganese are concentrated in laminated marls (manganese shales) of the lower Toarcian and lower to upper Jurassic red limestones.Carbonates of the system CaCO3–MnCO3–FeCO3, and minor quantities of braunite and pyrolusite are the prevailing primary manganese minerals. Characteristically they are associated with sedimentary iron minerals (hematite, goethite, Mn-siderite, chamosite, pyrite) showing a vertical sequence leading from weakly oxidzing to anaerobic conditions. In the red limestones pyrolusite and goethite are concentrated in carbonate-rich nodules and crusts. The manganese shale facies besides its elevated contents of Ca and SiO2 is characterized by Mn and Fe values which are closely correlated. In contrast to the average composition of comparable black shale and normal marine Mn and Fe deposits the trace element contents, partly correlated with manganese, are raised, as well.According to their mineralogical and chemical composition the manganese shales must be classed with volcanogenic sedimentary deposits. Volcanic activity during manganese deposition in the Northern Limestone Alps could be proved for the first time by celadonite-bearing tuffaceous layers in manganese carbonate sediments.

Mit 8 Abbildungen  相似文献   

11.
The compositional variations in epidotes, Ca2Al2(Fe3+, Al)-Si3O12(OH), from a prograde Mesozoic rock series in the Eastern Alps, Austria, are systematically related to metamorphic grade and the oxidation state of the rock. With increasing metamorphic grade the average composition of the zoned epidotes shifts to Fe3+-poorer compositions reflecting not only the effect of temperature and total pressure but also the concomitant decrease of the oxidation state of the rocks. Oxidized hematite-bearing assemblages are: 90 mole % Al2FeEp (greenschists) 70 mole % Al2FeEp (garnet amphibolites) 58 mole % Al2FeEp (eclogites); reduced sulfidebearing assemblages are: 42 mole % Al2FeEp (greenschists) 24 mole % Al2FeEp (garnet amphibolites) 23 mole % Al2FeEp (eclogites).A similar compositional evolution of the epidotes as in the spatial sequence of the samples can be observed within the single zoned crystals, reflecting the temporal changes of temperature, total pressure and oxygen fugacity during the prograde crystallization. The Fe3+-contents of core and rim decrease with increasing metamorphic grade and decreasing oxidation state. Generally the zoned epidotes consist of a Fe3+-rich core (90 to 63 mole % Al2FeEp) and a Fe3+-poorer rim (55 to 23 mole % Al2FeEp). Core and rim of the epidote crystals are separated by a compositional gap the extension of which is independent of the bulk rock composition, the oxidation state, and the mineralogical composition of the assemblages but becomes smaller with increasing metamorphic grade: 7253 mole % Al2FeEp (low grade greenschists, 400° C) 6355 mole % Al2FeEp (higher grade greenschists, 500° C), and 6055 mole % Al2FeEp (garnet amphibolites, 500–550° C). At the temperature conditions of the highest grade garnet amphibolites and eclogites (550° C) the compositional gap closes at a composition of 58 mole % Al2FeEp.The data presented thus confirm clearly the existence of an asymmetric miscibility gap in the monoclinic Al-Fe(III)-epidote solid solution series, which, for the first time, has been assumed by Strens (1964, 1965).A model is proposed that describes the prograde compositional evolution of the epidotes studied through the competing mechanisms of growth and diffusional Al-Fe3+ exchange and their dependence on metamorphic grade and oxidation state.  相似文献   

12.
Measurements of O2, Fe(II), Mn(II)and HS5 in salt marshsediments in the Tagus Estuary, Portugal, made with a voltammetric microelectrode, reveal strong seasonal differences in pore water composition within the 20~cm deep root zone. In spring, oxygen was below detection limit except close to the sediment surface. Fe(II) was present below 5 cm in concentrations ranging from detection limit to 1700 M. In summer, oxygen was present in the pore water almost to the bottom of the root zone in concentrations ranging from detection limit to more than 100 M. The spatial variability was intense: O2 concentrations as high as 78 M and as low as 25 M existed within 2~mm of each other. Fe(II) was below detection limit except towards the bottom of the root zone. In late fall, oxygen was found to 8 cm depth, but in concentrations lower than in summer, and Fe(II) was present below 9 cm. Mn(II) was found at levels declining from typical values of 200 M in spring to less than 20 M in late fall. With one exception, sulfide was below the detection limit in all measurements. During periods when dissolved Fe(II) is available in the pore water at the same time as 2 is delivered by roots, iron-rich concretions can form on roots. These conditions, which lead to precipitation of iron oxide in the sediment adjacent to roots, exist in spring, when new roots infiltrate anoxic Fe(II) containing sediment. They do not exist in summer, when dissolved Fe(II) is unavailable, or in winter, when oxygen is unavailable. The seasonal redox pattern revealed by the pore water chemistry is driven by the annual cycle of growth and decay of roots.  相似文献   

13.
The redox processes regulating transport of Mn in the water column of a eutrophic, dimictic lake (Lake Norrviken, Sweden) are interpreted based on a one-dimensional diffusion-reaction model for Mn(II). It is found that rates and rate constants for oxidation and reduction vary greatly with depth and also with time during the season of stratification. Calculated rates show that Mn(II) oxidation and reduction generally occur in narrow depth intervals (25–50 cm). This is in good agreement with measured profiles of particulate Mn (MnO x ). Maximum oxidation rate constants (assuming first order kinetics) at each date are in the first half of the season <1 d–1, but then increases to a rather constant value of about 25 d–1. These high rate constants are indicative of microbiological involvement in the Mn(II) oxidation. This is further evidenced by SEM-EDS analysis showing Mn enriched particles morphologically similar toMetallogenium. Reductive dissolution of Mn oxides occurs mainly in the zone just below the zone of maximum oxidation rate. The release of Mn(II) is accompanied by production of alkalinity and CO2. The relation between production rates of Mn(II) and alkalinity indicates that Mn oxides act as terminal electron acceptors in the bacterially mediated oxidation of organic matter. However, the Mn2+/CO2 ratio is significantly lower than what is expected from this process. It is suggested that the Mn reduction is coupled to fermentation. Close coexistence of Mn reduction and oxidation at high rates, such as found in the water column of this lake, facilitates rapid and continuous regeneration of reducible Mn oxides. This gives rise to a quantitatively important mechanism of organic matter oxidation in the water column.  相似文献   

14.
Zusammenfassung Ausgedehnte Granodiorit- und Granitmagmen intrudierten am Südrand des Rhodope-Massivs (Symvolongebirge und Kavala-Gebiet, Nordgriechenland) syntektonisch in bezug auf eine Formung, die durch überwiegend flach nach NE bis ENE tauchende Faltungs- und Scherungsachsen gekennzeichnet ist (B2-Tektonik). Die metamorphen Hüllgesteine wurden von der B2-Tektonik ebenfalls kräftig erfaßt. Ihr älteres Gefüge, das durch mittelsteil nach NNW tauchende B1-Achsen bestimmt war, kommt daher nur noch reliktisch vor. Der Mineralbestand sowohl der Magmatite als auch ihres metamorphen Rahmens wurde im Zuge der B2-Tektonik retrograd metamorph umgewandelt.Radiometrische Altersbestimmungen lassen erkennen, daß die magmatischen Gesteine spätestens im Oberkarbon kristallisierten, anschließend jedoch wiederholt aufgewärmt wurden. Das Alter der prämagmatischen Metamorphose der Hüllgesteine und der mit dieser in Zusammenhang stehenden B1-Tektonik kann demnach nicht jünger als kaledonisch sein.
Extensive granodioritic and granitic magmas were intruded in the southern margin of the Rhodope-Massif (Symvolon mountains and Kavala region, northern Greece). The intrusions took place syntectonically to a deformation which is characterized by predominantly gently NE to ENE plunging fold- and shear-axes (B2-folding). The mantling rocks, which have been metamorphosed long before this B2-folding have an older structure which is characterized by mediumly NNW plunging B1-axes, visible only in relicts. During the B2-folding the mineral contents of the igneous rocks and their metamorphic mantling rocks have been metamorphosed retrogressively.Radiometric dating indicates that the crystallization of the magmatic rocks have a minimum age of Upper-Carboniferous, but subsequently these rocks were reheated repeatedly. The age of the premagmatic metamorphism of the mantling rocks and that of the related B1-foldnig, therefore, cannot be younger than Caledonic.
Résumé Dans la partie sud du massif du Rhodope (montagnes du Symvolon et région de Kavala, Grèce du Nord) existent de grandes intrusions de magmas granodioritiques et granitiques. Les intrusions eurent lieu syntectoniquement au cours d'une phase de déformation caractérisée par des axes de plis et de cisaillement, généralement à plongement faible vers le NE à ENE (tectonique B2). Les roches encaissantes, qui furent métamorphisées longtemps avant cette phase de tectonique B2, ont une structure plus ancienne, caractérisée par des axes B1 plongeant moyennement vers le NNW. Cette structure est reconnaissable seulement dans des parties réiduelles. Durant la tectonique B2 les roches éruptives et les roches encaissantes métamorphisées subirent un métamorphisme rétrograde.Des datations radiométriques indiquent, pour la cristallisation des roches magmatiques, au minimum un âge Carbonifère supérieur. Dans la suite ces roches furent réchauffées â plusieures reprises. Le métamorphisme plus ancien des roches encaissantes et la tectonique B1 associée à ce métamorphisme ne peuvent donc pas Être plus récents que l'époque calédonienne.
Rhodope ( Symrolon Kavala, ) - . , , , , NE ENE (B2- ). 2. , B1 NNW, . , , . , , , , . , - B1 .
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15.
Mesothermal gold mineralization at the Samdong mine (5.5–13.5 g/ton Au), Youngdong mining district, is situated in massive quartz veins up to 1.2 m wide which fill fault fractures within upper amphibolite to epidote-amphibolite facies, Precambrian-banded biotite gneiss. The veins are mineralogically simple, consisting of iron- and base-metal sulfides and electrum, and are associated with weak hydrothermal alteration zones (<0.5 m wide) characterized by silicification and sericitization. Fluid inclusion data and equilibrium thermodynamic interpretation of mineral assemblages indicate that the quartz veins were formed at temperatures between 425 and 190°C from relatively dilute aqueous fluids (4.5–13.8 wt. % equiv NaCl) containing variable amounts of CO2 and CH4. Evidence of fluid unmixing (CO2 effervescence) during the early vein formation indicates approximate pressures of 1.3–1.9 kbars, corresponding to minimum depths of 5–7 km under a purely lithostatic pressure regime. Gold deposition occurred mainly at temperatures between 345 and 240 °C, likely due to decreases in sulfur activity accompanying fluid unmixing. The 34S values of sulfide minerals (-3.0 to 5.3 ), and the measured and calculated O-H isotope compositions of ore fluids (18O = 5.7 to 7.6; = –74 to –80) indicate that mesothermal gold mineralization at the Samdong mine may have formed from dominantly magmatic hydrothermal fluids, possibly related to intrusion of the nearby ilmenite-series, Kimcheon Granite of Late Jurassic age.  相似文献   

16.
Zusammenfassung Röntgenographische Untersuchungen an Einkristallen von Arsenbrackebuschit, Pb2(Fe, Zn)(OH, OH2) (AsO4)2 (mit FeZn21), ergaben die RaumgruppeP21/m mita 0=7,763(1) Å,b 0=6.046(1) Å,c 0=9.022(1)Å, =112,5(1)°,V=391,2(1) Å3,Z=2 und x =6,54 g/cm3. Dreidimensionale Fouriersynthesen und Verfeinerungen nach der Methode der kleinsten Quadrate bis zu einemR-Wert von 0,073 zeigten, daß das neue Mineral strukturell einer Gruppe von Blei-Mineralen der allgemeinen Formel Pb2 Me(Z) (XO4) (YO4) — mitMe=Cu2+, Mn2+, Zn2+, Fe3+;X=S, Cr, V, As;Y=P, As, V;Z=OH, OH2 — zuzuordnen ist. Vertreter dieser Gruppe sind z. B. Tsumebit Pb2Cu(OH) (SO4) (PO4), Vauquelinit Pb2Cu(OH) (CrO4) (PO4) und auch Brackebuschit Pb2(Mn, Fe) (OH2) (VO4)2. Strukturelle Verwandtschaft besteht mit Tsumcorit Pb(Zn, Fe)2(OH, OH2)2(AsO4)2, einem weiteren Blei-Arsenat der gleichen Lagerstätte.
Structural investigation of arsenbrackebuschite
Summary X-ray single crystal work on arsenbrackebuschite, Pb2(Fe, Zn) (OH, OH2) (AsO4)2 (with FeZn21), gave space groupP21/m witha 0=7.763(1),b 0=6.046(1),c 0=9.022(1) Å, =112.5(1)°,V=391.2(1) Å3,Z=2 and x =6,54 g/cm3. 3-dimensional Fourier syntheses and least-squares refinement (finalR=0.073) showed that the new mineral belongs to a group of lead minerals with the general formula Pb2 Me(Z) (XO4) (YO4)Me=Cu2+, Mn2+, Zn2+, Fe2+, Fe3+;X=S, Cr, V, As; Y=P, As, V;Z=OH, OH2. Members of this group, are for example tsumebite, Pb2Cu(OH) (SO4)(PO4), vauquelinite, Pb2Cu(OH) (CrO4) (PO4), and brackebuschite, Pb2 (Mn, Fe) (OH2) (VO4)2. A structural relationship exists to tsumcorite, Pb(Zn, Fe)2(OH, OH2)2 (AsO4)2, another lead-arsenate from Tsumeb.

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17.
Analyses for the following elements were made on 118 samples of pore water and 23 samples of sea water from the radiolarian ooze area of the Central Pacific: Na, Ca, Br, Sr (major elements) and Sc, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Rb, Ag, Sb, Cs, Eu, Ta, Hg, U.The average concentration of most of the elements analyzed is higher in the pore water than in the sea water. The enrichment of elements in both the pore water and the bottom near sea water relative to the average composition of the sea water depends on the residence times of the elements in the sea water — the shorter the residence time the greater the enrichment.The enrichment of an element in these sea and pore waters is also dependant on the chemical species in which it occurs in the sea water. The enrichment seems to be greater for hydroxides, less for complex chloride ions and there is no enrichment for simple ions. The enrichment of the elements occuring as hydroxides (Fe, Cu, Cr, Sc, Eu) or complex chlorides (Mn, Ni, Co, Zn, Ag, Hg, Se) results in precipitation from the sea water, which contributes to the growth of the manganese nodules as well as to the genesis of metalliferous sediments in this area. The greater enrichment in the pore water relative to the sea water accounts for the remobilization of these elements from the sediment as the main source of the material for the growth of the manganese nodules.
Zusammenfassung 118 Porenwasser- und 23 Meerwasser-Proben aus dem Radiolarienschlammgebiet des Mittleren Pazifik wurden auf folgende Elemente analysiert: Na, Ca, Br, Sr (Hauptbestandteile) und Sc, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Rb, Ag, Sb, Cs, Eu, Ta, Hg, U.Die durchschnittliche Konzentration der meisten bestimmten Elemente ist im Porenwasser höher als im Meerwasser. Die Elementaranreicherung sowohl im Porenwie im bodennahen Meereswasser ist im Vergleich zur weltweiten Durchschnittszusammensetzung des Meerwassers abhÄngig von den Verweilzeiten der Elemente im Meer — je kürzer die Verweilzeit, desto grö\er die Anreicherung.Die Anreicherung eines Elements in diesen Meeres- und PorenwÄssern hÄngt auch von der chemischen Spezies ab, in der es im Meerwasser vorkommt. Die Anreicherung scheint grö\er zu sein für Hydroxide, geringer für komplexe Chlorid-Ionen, und es gibt keine Anreicherung für einfache Ionen. Die Anreicherung der Elemente, die als Hydroxide (Fe, Cu, Cr, Se, Eu) oder komplexe Chloride (Mn, Ni, Co, Zn, Ag, Hg, Se) vorkommen, führt zur AusfÄllung aus dem Meereswasser. Diese AusfÄllung trÄgt bei zum Wachstum der Manganknollen und zur Entstehung von metalliferous sediments in diesem Gebiet. Die grö\ere Anreicherung im Porenwasser im Vergleich zum Meereswasser spricht für die Mobilisierung dieser Elemente aus dem Sediment als der wichtigsten Materialquelle für das Wachstum der Manganknollen.
Résumé Dans la région des boues á radiolaires de l'Océan Pacifique central 118 échantillons d'eau interstitielle et 23 échantillons d'eau de mer ont été prélevés et analysés. Les éléments suivants ont été déterminés: Na, Ca, Br, Sr (éléments principaux) et Sc, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Rb, Ag, Sb, Cs, Eu, Ta, Hg, U.La concentration moyenne de la majorité des éléments analysés est plus grande dans l'eau interstitielle que dans l'eau de mer. L'enrichissement des éléments dans l'eau interstitielle ainsi que dans l'eau de mer près du fond, comparé aux valeurs moyennes dans l'eau de mer, dépend du temps de séjour de l'élément dans l'eau de mer — le plus court est le temps du séjour, plus fort est l'enrichissement.L'enrichissement d'un élément dans ces échantillons d'eau interstitielle et d'eau de mer dépend également de la forme chimique sous laquelle il se trouve dans l'eau de mer. Il semble que l'enrichissement est plus fort pour les hydroxides, et moindre pour les ions chlorurés complexes. Il n'ya pas d'enrichissement en ions simples. L'enrichissement des éléments sous forme d'hydroxides (Fe, Cu, Cr, Sc, Eu) ou de chlorures complexes (Mn, Ni, Co, Zn, Ag, Hg, Se) entraine la précipitation de ces éléments hors de l'eau de mer, ce qui contribut à la croissance des nodules de manganèse ainsi qu'à la genèse des sédiments métallifères dans cette région. L'enrichissement plus fort dans l'eau interstitielle par rapport à l'eau de mer rend compte de la remobilisation de ces éléments à partir du sédiment comme source principale de matière pour la croissance des nodules de manganèse.
118 23 : Na, , Br, Sr ( ) Sc, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Rb, Ag, Sb, Cs, u, , Hg, U. , . , , — , . - , : , . — Fe, Cu, Cr, Sc, u -, — Mn, Ni, , Zn, Ag, Hg, Se - . , . 3 , , .
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18.
An experimental study of the system Zr-Fe-Ti-O in equilibrium with metallic iron has been conducted at atmospheric pressure and in the temperature range 950–1300° C, with the purpose of modelling sub-solidus relations between Zr-bearing Fe-Ti oxide phases in lunar rocks. The phase relations are governed by the coexistence of the Fe-Ti oxides with ZrO2 at temperatures below 1247° C, but with the new cubic ZFT phase at higher temperatures. ZFT, approximately Zr Fe Ti O5, is probably related to the so-called stabilized cubic zirconia and could represent a synthetic equivalent of some lunar Zr-Fe-Ti rich oxide minerals.The zirconium contents in all Fe-, Ti and Fe-Ti-oxide phases increase with increasing temperature. At each temperature, Zr is incorporated preferentially in the Ti-oxide (up to 11 wt% ZrO2), followed by ferropseudobrookite (up to 6 wt% ZrO2), ilmenite (max. 4 wt%) and wüstite (max. 2.5 wt%). Ulvöspinel coexisting with ilmenite (+Fe0+ ZrO2 and/or ZFT) always contains less than 1.2 wt% ZrO2, whereas the same mineral in assemblage with wüstite-ZrO2-Fe0 displays even higher ZrO2 contents than ilmenite (above 4 wt%). Considering that the values determined here in the synthetic parageneses represent saturation concentrations at high temperatures in a simple model system, the ZrO2 concentrations in the corresponding lunar minerals should generally be significantly lower. This is realized, except for the so-called Cr-Zr-Ca armalcolites which display ZrO2 contents in the range 3.5–7 wt% and are thus probably related rather to Zr-rich oxide minerals than to armalcolite itself.  相似文献   

19.
Staurolite and corundum are found as inclusions in tourmaline in a talc-phlogopite-chlorite-albite chist near Mount Bernstein (71°37S, 163°07E), northern Victoria Land, Antarctica. These inclusions are interpreted as relics of a staurolite-talc-corundum-chlorite assemblage that was stable during an early stage in the metamorphic cycle and subsequently armored by tourmaline, probably during the middle stage. Pressures and temperatures during the middle stage are estimated to be 650–700°C and 5.5–6.4 kbar. The transition from the early to the middle stage represents a roughly isothermal decrease in pressure of 2–3 kbar. During a late retrograde stage (T=300–370°C, P=3–5 kbar), staurolite was partly replaced by a muscovitic aggregate containing clinozoisite, pumpellyite, and margarite.The staurolite is unusually Si-poor (26.77, 25.85 weight % SiO2 or 7.275, 7.091 Si per formula unit for 46 oxygens anhydrous), Al-rich (58.00, 57.85% Al2O3, 18.579, 18.702 Al), low in divalent cations (Fe+Mg+Mn+Zn=3.301, 3.560) and magnesian (atomic Mg/(Mg+Fe)=0.42, 0.40). Ion microprobe analysis of the first grain indicates about 0.2% Li2O (0.219 Li) is present. The following substitutions are proposed to explain the unusual chemistry of this staurolite (crystallographic site notation of Smith 1968, in bold letters): Al(Si)+Al(Al(3A,B))Si(Si)+Fe(Fe), Li(Fe)+Al(Al(3A,B))2 Fe(Fe), and 2 Al(Al(3A,B)) 3 Fe(Fe).According to a pressure-temperature diagram constructed by the method of Schreinemakers for the model system FeO-MgO-Al2O3-SiO2 (H2O in excess), the talc-staurolite assemblage should be stable only in quartz-free rocks at temperatures near 700° C and pressures of 8 kbar or more. The rarity of the staurolite-talc assemblage even in Mg-Al-rich rocks metamorphosed at the appropriate pressure-temperature conditions is attributed to the appearance of anthophyllite or, in Na2O-bearing rocks, gedrite. Orthoamphibole-cordierite and orthoamphibolekyanite assemblages with chlorite or corundum are incompatible with staurolite-talc±albite. In rocks lacking corundum and formed at pressures above the stability limit of cordierite, staurolite-talc may be metastable relative to orthoamphibole-kyanite, while in corundum-bearing rocks, staurolite-talc may appear under certain conditions, possibly at higher water activities than the orthoamphibole-kyanite assemblage.  相似文献   

20.
Summary In 1961–63 the Czechoslovakian Geological Survey drilled a 1596 m deep borehole in the Sn-W-mineralized Cinovec (Zinnwald) granite cupola. The hole traversed zinnwaldite granite (ZG) to 730 m, then protolithionite granite (PG). The boundary between the two granites is a transition zone (TZ) about 10 m thick. The oxides of Nb, Ta and Ti, present in accessory amounts, are columbite, ilmenorutile, rutile and pyrochlore. The columbite occurs in both granites, but in the PG only below 1558 m depth. Its crystals are strongly zoned, the zoning representing variations in Nb/(Nb + Ta) on the one hand, and non-uniform distribution of W on the other. The columbite in the TZ is strongly enriched in W, up to 32.6 wt% WO3. The columbites with W < M4+ show the substitutions W6+ + M4+ 2(Nb, Ta)5+, where (M4+ = Ti, Sn, Th, U, Zr) and 6M4+ + 3M3+ 4Fe2+ 5(Nb, Ta)5+, where (M3+ = Sc, Y). In columbites with W > M4+, tungsten is introduced by the substitution W6+ + M4+ 2(Nb, Ta)5+, but also through the appearance of Fe3+ in the B site according to the replacement 2W6+ + Fe3+ 3(Nb, Ta)5+. The ratio Fe/(Fe + Mn + Ca) increases with depth, and Nb/(Nb + Ta) is higher in the PG.The ZG is characterized by the presence of ilmenorutile, which does not occur in the PG, where rutile contains at most only 4 wt% Nb2O5. Two types of substitution have been found in the ilmenorutile: Fe3+ + (Nb, Ta)5+ 2Ti4+; (Fe, Mn)2+ + 2(Nb, Ta)5+ 3Ti4-. For the ilmenorutiles studied, the ratio [Fe3+/(Fe, Mn)2+]at is near 1.AU- and Nb-rich phase, containing up to 36.2 wt% UO2, included in protolithionite, and missing from the ZG, has the composition of a defect pyrochlore, A2+ 2 5+(O6), and forms a solid solution with U4+B2 4+(O6]), where B4-= Ti, Si, Zr, Sn. Electron microprobe analyses indicate that this phase is strongly hydrated.The crystal chemistry of Nb-, Ta- and Ti-oxides in the Cinovec cupola reflects the complex geochemistry of its component granites and the interaction of the minerals with an F- and CO2-rich fluid phase. Among the thermodynamic parameters, fO2 plays a predominant role in the early evolutionary stages.
Résumé Un sondage profond (jusqu'à -1596m), a été réalisé en 1961–63 par le Service géologique tchécoslovaque, dans la coupole granitique, minéralisée en Sn-W, de Cinovec (Zinnwald), République tchèque. Ce sondage a recoupé un granite à zinnwaldite (ZG), relayé en profondeur (–730 m) par un granite à protolithionite (PG). Le contact entre ces deux granites est matérialisé par une zone de transition (TZ) puissante de 10 m environ. Les oxydes de Nb, Ta et Ti, présents en quantité accessoire, sont représentés par: columbite, ilménorutile, rutile et pyrochlore.La columbite apparaît tant dans ZG que dans PG, mais dans ce dernier uniquement dans la zone profonde (-1558.0 m). Ses cristaux sont fortement zonés. Le zonage reflète des variations du rapport Nb/(Nb + Ta) d'une part et une distribution hétérogène de W, d'autre part. La columbite de la zone de transition ZG-PG est très enrichie en W (jusqu'à 32.6 wt.~/ 0 W03). Les coiumbites à W < SM4+ présentent des substitutions W6+ + M4+ 2(Nb, Ta)5+, où (M44+ = Ti, Sn, Th, U, Zr) et 6M4+ + 3M3+ 4Fe2+ + 5(Nb, Ta)5-, où (M3+ = Se, Y). Dans celles à W > EM4+, outre la substitution W6+ + M4+ 2(Nb, T)5+, le tungstène est introduit grâce à l'apparition de Fe 3+ sur le site B suivant le schéma: 2W6+ + Fe3+ 3(Nb, Ta)5+. Le rapport Fe/(Fe + Mn + Ca) croit avec profondeur; celui Nb/(Nb + Ta) augmente dans PG.Le ZG est caractérisé par la présence de l'ilménorutile; par contre, celui-ci est absent dans PG, oú le rutile ne contient que 4 wt.% Nb205 au maximum. Deux types de substitution sont mis en évidence dans l'ilménorutile: Fe3+ + (Nb, Ta)5+ 2Ti4+; (Fe, Mn)2+ + 2(Nb, Ta)5+ 3Ti4+. Pour les ilménorutiles étudiés, le rapport [Fe3+/(Fe, Mn)2+]à, est proche de 1.Une phase riche en U (jusqu'à 36.2 wt.% UO2) et Nb, incluse dans la protolithionite et absente dans ZG, a composition d'un pyrochlore lacunaire A2+[B2 5+(06), formant une solution solide avec U4+E:B24+(O6), où B4+ = Ti, Si, Zr, Sn. Les analyses à la microsonde électronique indiquent que cette phase est fortement hydratée.La cristallochimie des oxydes de Nb, Ta et Ti dans la coupole de Cinovec reflète tant la complexité géochimique des granites qui la composent que l'interaction des minéraux avec une phase fluide riche en F et CO,. Parmi les paramètres thermodynamiques, fO2 joue un râle prépondérant lors des stades d'évolution précoces.
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