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1.
Carbon and oxygen isotope analyses were made of representative samples of calcite and quartz from the carbonate deposits in the Tolfa Mountains mining district. Measurements were also made of hydrogen isotope compositions, filling temperatures and salinities of fluid inclusions in these minerals. There are three stages of mineralization at Tolfa. In stage I, characterized by calc-silicate hornfels, the carbonates have relatively high 18O values of 14.5 to 21.6 suggesting a rather low water/rock ratio. 13C values of –0.3 to 2.1 indicate that appreciable decarbonation or introduction of deep-seated carbon did not occur. Stage II is marked by phanerocrystalline carbonates; 18O values of 13.1 to 20.0 and 13C values of 0.7 to 5.0 identify them as hydrothermal veins rather than marbles. D values of –56 to –50 for inclusion fluids suggest a possible magmatic component to the hydrothermal fluid. Filling temperatures of coarse-grained samples of Calcite II are 309° to 362° C with a salinity range of 5.3 to 7.1 weight percent NaCl. Calculated 18O values of 11–12 for these fluids are again indicative of low water/rock ratios. The sparry calcites of stage III have 18O and 13C values of 8.1 to 12.9 and –1.7 to 3.2, respectively. D values of inclusion fluids are –40 to –33, clearly heavier than in earlier stages and similar to values of modern local ground waters. A salinity measurement of <0.1 weight percent NaCl in a sample of Calcite III is compatible with a relatively unaltered ground water origin for this fluid. Precipitation of the sparry calcite took place at much lower temperatures, around 160° C. For quartz, 18O values of 9.3 to 12.4 and D values for inclusions of –53 to –28 are consistent with its late occurrence and paragenetic link with associated carbonates. 相似文献
2.
The Yaoan vein-type gold deposit is located in the Ailaoshan-Jinshajiang alkaline intrusive belt, Yunnan Province, China, and is associated both in time and space with 33.5±1.0-Ma-old alkaline intrusions. The gold mineralization is associated with potassic wall-rock alteration. The REE distribution patterns of secondary K-feldspar are generally similar to those of the igneous perthite but with about seven times higher total REE abundances. The alteration is ascribed to a high-REE magmatic fluid derived from the Yaoan alkaline intrusive suite. The hydrothermal Yaoan gold deposit formed during two gold-bearing stages, i.e. a sulfide (pyrite) stage and a sulfide-oxide stage (pyrite-specularite). The REE abundance of early stage I pyrite is relatively high with strong enrichment in LREE, (La/Yb)n of 40–290, generally positive Eu anomalies (Eu/Eu*=0.86–1.55), and REE patterns very similar to those of secondary feldspar. In contrast, the later stage II pyrite has much lower REE concentrations and lower (La/Yb)n of 5.5–11.8, Eu/Eu* of 0.49–0.76, and flat chondrite-normalized spidergram patterns. The stage I pyrite has 34S in the range of –2.2 to +3.2, and overlaps with regionally distributed pyrite in least-altered syenite porphyry. In contrast, stage II pyrite has much higher 34S values between +7.8 and +16.5. Carbon isotope data for four samples from stage II revealed 13C (PDB) values between –6 and –8. These stable isotope and REE data suggest that magmatic fluids of the alkaline intrusions caused both potassic alteration and stage I sulfide mineralization. The system evolved from stage I to stage II mineralization by influx of meteoric fluids with relatively heavier sulfur, although calcite carbon isotope data suggest that the CO2 remained dominantly of magmatic origin.Editorial handling: B. Lehmann 相似文献
3.
R. Kerrich W. S. Fyfe R. L. Barnett B. B. Blair L. M. Willmore 《Contributions to Mineralogy and Petrology》1987,95(4):481-498
Monomineralic domains of chlorite, corundum and Cr muscovite coexist over a kilometer scale within ultramafic schists of the Harare greenstone belt (2.73 Ga). This exotic lithological association includes the conjunction of some of the most aluminous (Al2O388 wt%) and potassic (K2O10 wt%) rocks known. The paragenetic sequence developed from chloritecorundumcorundum+ diaspore: Cr muscovite variably overprinted both the corundum and chloritite domains. Terminal stages were marked by sporadic production of andalusite+quartz, and finally margarite.Chlorite (Cr2O3=0.31–2.65 wt%), corundum (0.79–2.66 wt%), and diaspore are all Cr-rich varieties. The chromian (Cr2O33.86 wt%) paragonitic muscovite incorporates up to 17% of the paragonite molecule, and significant Mg and Fe substitutions.The suite of rocks are characterized by chondritic Ti/Zr ratios (–x=107), systematically enhanced Cr (up to 14000 ppm) and Ni (up to 1200 ppm) abundances, low levels of the alteration-insensitive incompatible elements Th, Ta, Nb. Chlorite, corundum and Cr muscovite represent progressive stages in the incremental metasomatic alteration of a komatiite precursor. Mass balance calculations, constrained by the isochemical behaviour of Ti, Zr and Hf reveal that the komatiite chloritite transformation involved volumetric contractions of 60% by hydrothermal leaching of Si, Fe, Mn, Ca and Na. Reaction of chloritite to corundum involved further volumetric reductions of 50% due to essentially quantitative loss of Si, Fe, Mn, Mg, K and Ca. Conversion of corundum to muscovite required additions of Si, K, Fe, Mn, Mg, Rb and Ba at 50–200% dilation. K, Rb, Ba, Li and Cs are enriched by up to 2×103 over background abundances in ultramafic rocks, and the suite is also enriched in B, Se, Te, Bi, As, Sb and Au. REE were extensively leached during chloritite-corundum stages, whereas LREE additions accompany development of muscovite. Ti, Zr, Hf and Al were all concentrated by selective leaching of mobile components, but absolute additions of Al accompanied development of the corundum domains due to Al precipitation in response to depressurization.Corundum (
18O=3.5–4.8), muscovite (
18O=6.7–7.5) and chlorite (4.5–5.6) are isotopically uniform and formed at 380–520° C from a fluid where
18O=5.6–6.9. The corundum is 18O depleted relative to either igneous or anatectic counterparts (Ocor=7.6–8.2), or to gibbsitic laterites (
18O=12–17).Previous genetic schemes involving metamorphism of exhalites or bauxite, or Si-undersaturation of magmas, can all be ruled out from the data. The chloritite, corundum, Cr-muscovite association represents sequential alteration products of ultramafic rocks by high temperature, low pH hydrothermal solutions carrying LIL-elements, and in which excursions of pH and/or degree of quartz undersaturation account for the mineralogical transitions. A deep level acid epithermal system, or fluid advection across steep inverted thermal gradients in a thrust regime could account for required hydrothermal conditions. 相似文献
4.
Stable isotope geochemistry of the Archean Val-d‘Or (Canada) orogenic gold vein field 总被引：2，自引：0，他引：2
A systematic study of the auriferous quartz veins of the Val-dOr vein field, Abitibi, Quebec, Canada, demonstrates that the C, O, S isotope composition of silicate, carbonate, borate, oxide, tungstate and sulphide minerals have a range in composition comparable to that previously determined for the whole Superior Province. The oxygen isotope composition of quartz from early quartz–carbonate auriferous veins ranges from 9.4 to 14.4 whereas later quartz-tourmaline-carbonate veins have 18Oquartz values ranging from 9.2 to 13.8 . Quartz-carbonate veins have carbonate (18O: 6.9–12.5 ; 13C: –6.2– –1.9 ) and pyrite (34S: 1.2 and 1.9 ) isotope compositions comparable to those of quartz-tourmaline-carbonate veins (18O: 7.9–11.7 ; 13C: –8.0 – –2.4 ; 34S: 0.6–6.0 ). 18Oquartz values in quartz-tourmaline-carbonate veins have a variance comparable to analytical uncertainty at the scale of one locality, irrespective of the type of structure, the texture of the quartz or its position along strike, across strike or down-dip a vein. In contrast, the oxygen isotope composition of quartz in quartz-tourmaline-carbonate veins displays a regional distribution with higher 18O values in the south-central part of the vein field near the Cadillac Tectonic Zone, and which 18O values decrease regularly towards the north. Another zone of high 18O values in the northeast corner of the region and along the trace of the Senneville Fault is separated by a valley of lower 18O values from the higher values near the Cadillac Tectonic Zone. Oxygen isotope isopleths cut across lithological contacts and tectonic structures. This regional pattern in quartz-tourmaline-carbonate veins is interpreted to be a product of reaction with country rocks and mixing between (1) a deep-seated hydrothermal fluid of metamorphic origin with minimum 18O=8.5 , 13C=0.6 and 34S=–0.4 , and (2) a supracrustal fluid, most likely Archean seawater with a long history of water-rock exchange and with maximum 18O=3.9 , 13 C=–5.6 and 34S=5.0 . 相似文献
5.
Sulphur isotope measurements on five Australian stratiform lead-zinc sulphide ores are presented. Each deposit is characterised by a conspicuously narrow spread of values, mean 34S heavier than meteoritic, average crustal, and, where sampled stratigraphically, 34S related to stratigraphy rather than propinquity. When considered with other deposits of the same class from elsewhere, several seemingly general features appear: Mean 34S heavier than meteoritics; ranges for individual deposits narrow and rarely more than 8 with standard deviation approximately 1 to 2; individual values for the whole group spread between, but almost entirely restricted by, the values for meteoritic S and seawater SO4
—; no age effect; no apparent relationship between 34S and lead type; and, where investigated, a stratigraphical affiliation. While no positive interpretation of these features is made, it is suggested that the sulphur concerned has been derived neither from migrant hydro-thermal solutions nor from the H2S of normal biological sulphate reduction in seawater.
Zusammenfassung Es werden Meßergebnisse von fünf australischen geschichteten Blei-Zink-Sulfid-Lagerstätten mitgeteilt: Jedes Vorkommen ist durch einen bemerkenswert engen Schwankungsbereich der Werte, Mittelwert 34S schwerer als meteoritischer Schwefel/Durchschnittswert aus der Erdkruste, gekennzeichnet. Wo die Proben in stratigraphischer Abfolge entnommen wurden, zeigt der Wert 34S eine stärkere Affinität zur Stratigraphie als zu absoluter Entfernung der Muster. Vergleicht man diese Werte mit solchen von anderen Vorkommen der nämlichen Lagerstättengruppe, so liegen einige allgemeine Eigenheiten auf der Hand: Für einige Vorkommen ist der Mittelwert 34S schwerer als meteoritischer Schwefel; für einzelne Lagerstätten ist der Bereich eng und überschreitet kaum mehr als 8 mit der Standardabweichung von ungefähr 1 bis 2; Einzelwerte für die gesamte Lagerstättengruppe fallen fast ausschließlich zwischen die Werte für meteoritischen Schwefel und SO4 2–-Ionen im Meerwasser; es herrscht kein dem geologischen Alter zuzuschreibender Effekt; auch gibt es keine augenscheinliche Beziehung zwischen dem 34S-Wert und dem Blei-Typ; in jenen Fällen aber, wo Untersuchungsergebnisse vorliegen, ist eine Beziehung der Werte zur Stratigraphie zu erkennen. Obwohl keine positive Interpretation dieser Phänomena angestellt wurde, wird die Vermutung geäußert, daß der betreffende sulfidische Schwefel weder von wandernden hydrothermalen Lösungen noch vom H2S einer normalen biologischen Sulfatreduktion im Meerwasser abgeleitet werden kann.相似文献
6.
Prof. Dr. Otto F. Geyer 《International Journal of Earth Sciences》1980,69(3):875-891
Zusammenfassung Die weit über 100 sedimentären Formationen und Gruppen im mesozoischen epikontinentalen bis kontinentalen Oriente Andino der nördlichen Anden (Peru, Ekuador und Kolumbien) werden 6 zeitlich aufeinanderfolgenden Magnafazies-Einheiten zugeordnet. Dabei zeichnet sich deutlich eine einheitliche paläogeographisch-sedimentäre Entwicklung in den genannten Räumen ab, obwohl sich der geologische Bau der andinen West- bzw. Küstenkordilleren im Norden (Kolumbien, Ekuador) grundsätzlich vom Süden (Peru, Chile) unterscheidet.
Der Verf. dankt der Deutschen Forschungsgemeinschaft (Bonn-Bad Godesberg) für Reisebeihilfen während der Jahre 1966 bis 1977. 相似文献
Over 100 sedimentary formations and groups are known from the epicontinental to continental Mesozoic (Oriente Andino sensu H.Bürgl) in the Andean region of Peru, Ecuador and Colombia. These lithostratigraphic (or facial) complexes are attached to 6 magnafacies-units which follow each other chronologically, thereby clearly evidencing a uniform paleogeographic-sedimentary development in the mentioned areas, although the geological structure of the Western respectively Coastal Cordilleras of the North (Colombia, Ecuador) is fundamentally different from that of the Southern ones (Peru, Chile).
Resumen Más de 100 grupos y formaciones sedimentarios des »Oriente Andino« (sensu H.Bürgl) en los Andes septentrionales (PerÚ, Ecuador, Colombia) están asociados a 6 unidades magnafaciales que se suceden cronológicamente. Este »Oriente Andino« abarca las cuencas sedimentarias de tipo epicontiental a continental de la época mesozoica. Se bosqueja así claramente, en las áreas mencionadas, una evolución paleogeográfica-sedimentológica bastante uniforme, aunque las estructuras geológicas de las Cordilleras Occidentales (o Costeras, respectivamente) de la parte septentrional (Colombia, Ecuador) se diferencian fundamentalmente de las del Sur (PerÚ, Chile).
100 Oriente Andine (, ) 6 . , ( , ) (, ).
Der Verf. dankt der Deutschen Forschungsgemeinschaft (Bonn-Bad Godesberg) für Reisebeihilfen während der Jahre 1966 bis 1977. 相似文献
7.
The 620 M.y.-old in Hihaou (In Zize) magmatic complex located at the north-western boundary of the Archaean In Ouzzal block (western Ahaggar), is composed of massive alkaline rhyo-ignimbrites and rhyolitic domes, which are intruded by a granophyric and granitic body. The whole is preserved in a cauldron structure. Extrusive rocks are strongly 18O-depleted, with -values as low as –1.5/SMOW, while granophyres are less depleted (minimum -18O value=+2.0/SMOW. The granite has values around + 6/SMOW. D/H compositions are rather low, with D–90 to –110/SMOW. Isotopic zoning of quartz phenocrysts, 18O/16O fractionation among coexisting phases, and heterogeneity of the whole-rock -18O values, suggest that the volcanic rocks have interacted with meteoric water after the eruption. Several mechanisms of isotopic alteration are discussed. The hydrothermal alteration does not seem to have been controlled by the granitic intrusion, but rather seems to have followed the deposition of thick pyroclastic deposits on permeable arkosic sandstones and fluvio-glacial conglomerates. Pervasive circulation of water through the cooling volcanic deposits could have produced the observed 18O depletion. 相似文献
8.
Summary Pervasive hydrothermal alteration zones in quartz-feldspar porphyry domes underly all massive sulfide lenses in the D-68 Zone Cu-Zn deposit, Noranda. Alteration pipes are mineralogically zoned and contain chloritic cores consisting of stringer sulfides, enveloped by sericitic haloes. Silicified rocks are found locally.Alteration took place at nearly constant volume. Na depletion, and K enrichment relative to the least altered rocks, are found in all alteration zones. Fe and Mg have been added to the chloritic zone and subtracted in the sericitic and silicic zones. Ca and Si are enriched mainly in the silicic zone. Al, Ti and Zr were the least mobile of the elements studied.Whole-rock 18O values vary from +5.6 to +6.2 per mil in chloritized rocks, +5.8 to + 7.3 per mil in sericitized rocks and + 7.2 to + 8.3 per mil in silicified rocks. D values for two chloritized samples are – 63 and – 70 per mil whereas in two sericitized samples they are close to –62 per mil. Quartz from the chlorite alteration zone is isotopically heavier (18O = 8.6 per mil) than that from the sericite alteration zone (18O = 6.4 per mil), suggesting equilibration with different hydrothermal fluid or different temperature of alteration. Assuming an alteration temperature of 300° + 50°C the fluid in equilibrium with quartz and chlorite had 18O and D values of about 1.5 ± 2.0 per mil and –23 ± 5 per mil, respectively. The fluid in equilibrium with quartz and sericite had 18O and D values of about –0.5 ± 2 per mil and –30 ± 5 per mil, respectively. On the basis of isotopic data, seawater was probably the major constituent of the hydrothermal fluids.
With 7 Figures 相似文献
Hydrothermale Umwandlung und Sauerstoff-Wasserstoff-Isotopengeochemie der Zone D-68 Cu-Zn Derberz Sulfidlagerstätte, Noranda District, Quebec, Canada
Zusammenfassung Hydrothermale Umwandlungszonen in porphyrischen Quarz-Feldspat Gesteinskörpern liegen unterhalb von Derberz Sulfidlinsen in der D-68 Zone Cu-Zn Lagerstätte, Noranda. Umgewandelte pipes sind mineralogisch zoniert; sie enthalten aus Sulfiden bestehende chloritische Kerne, die von sericitischen Höfen umhüllt werden. Lokal treten silicifizierte Gesteine auf.Die Umwandlung ging bei annähernd konstantem Volumen vor sich. Na-Verarmung und K-Anreicherung, bezogen auf die am wenigsten umgewandelten Gesteine, liegen in allen Umwandlungszonen vor. Fe und Mg wurden der Chloritzone zugeführt, in den Sericit- und Si-Zonen abgeführt. Ca und Si sind vor allem in der Si-Zone angereichert. Al, Ti und Zr waren von den untersuchten Elementen am wenigsten mobil.Gesamtgesteins-18O Werte variieren von +5,6 bis +6,2 in den chloritisierten Gesteinen, von +5,8 bis 7,3 in sericitisierten Gesteinen und von +7,2 bis +8,3 in den silicifizierten Gesteinen. Die D Werte für zwei chloritisierte Proben betragen –63 und –70, in zwei sericitisierten Proben liegen sie hingegen nahe bei –62. Quarz von der Chlorit-Umwandlungszone ist isotopisch schwerer (18O = 8,6) als von der Sericit-Umwandlungszone (18O = 6.4), was eine Gleichgewichtseinstellung mit verschiedenen hydrothermalen Lösungen oder eine verschiedene Umwandlungstemperatur nahelegt. Bei einer angenommenen Umwandlungstemperatur von 300 ± 50°C, hatte die im Gleichgewicht mit Quarz und Chlorit stehende Lösung 18O und D Werte von etwa 1,5 ± 2 bzw. –23 + 5. Die im Gleichgewicht mit Quarz und Sericit befindliche Lösung hatte 18O und D Werte von etwa –0,5 ± 2%o bzw. –30 ± 5. Aufgrund der Isotopendaten war wahrscheinlich Meerwasser der Hauptbestandteil der hydrothermalen Lösungen.
With 7 Figures 相似文献
9.
Lavrushin V. Yu. Kopf A. Deyhle A. Stepanets M. I. 《Lithology and Mineral Resources》2003,38(2):120-153
Temperatures of the formation of mud-volcanic waters are determined based on concentrations of some temperature-dependent components (Na–Li, Mg–Li). Estimates obtained for the Taman and Kakhetia regions are similar and range from 45 to 170°, which correspond to depths of 1–4.5 km. The calculated temperatures correlate with the chemical (Li, Rb, Cs, Sr, Ba, B, I, and HCO3) composition of water and 13 (2) and 13 (CH4) values in spontaneous gases. The isotope values indicate that mechanisms of the formation of 13-rich gases, i.e., gases with high 13 values (up to +16.0 in 2 and –23.4 in CH4) in mud-volcanic systems of Taman and Kakhetia are governed by fluid-generation temperatures rather than the supply of abyssal gases. The 11 value was determined for the first time in mud-volcanic products of the Caucasus region. This value ranges from +22.5 to +39.4 in the volcanic water of Georgia, from –1.2 to +7.4 in the clayey pulp of Georgia, and from –7.6 to +13.2 in the clayey pulp of Taman. It is shown that the 11 value in clay correlates with the fluid-generation temperature and 11 correlates with 13 in carbon-bearing gases. These correlations probably testify to the formation of different phases of mud-volcanic emanations in a single geochemical system and suggest the crucial role of temperature in the development of isotope-geochemical features. 相似文献
10.
Zusmmenfassung Die Ergebnisse der Schwefelisotopenanalysen von sechs Sulfid- und vier Sulfatmineralproben von Bleiberg/Kreuth (Österreich) variieren von –6,9 bis –25,9 34S in den Sulfiden und von +14,8 bis +18,9 34S in den Sulfaten. Die große Variationsbreite der Schwefelisotopen und die Bevorzugung des leichten Schwefels deutet vermutlich auf bakterielle Prozesse der Sulfidfällung. Die Sulfatschwefel fallen in den Bereich der Schwefelisotopenzusammensetzung des mesozoischen (postskytischen) Meerwassers.
Determination of the sulfur isotopic composition in some sulfide and sulfate minerals of the lead zinc deposit, Bleiberg/Kreuth, Carinthia
Summary Results of sulfur isotope analyses on 6 sulfides and 4 sulfates from Bleiberg/Kreuth (Austria) range from –6.9 to –25.9 34S (in sulfides) and from +14.8 to +18.9 34S (in sulfates). A large range of sulfide sulfur isotope fractionation with appreciable light sulfur probably indicates a bacterial sulfur source in sulfide precipiation. The sulfate sulfur plots in the range of Mesozoic (post-Skytian) seawater sulfur isotopic composition.相似文献
11.
M. Deb 《Mineralium Deposita》1986,21(4):313-321
The sulfur isotope composition of 86 sulfide minerals from the Middle Proterozoic, metamorphosed, stratiform, sediment-hosted Zn-Pb-CU sulfide deposits of Dariba and Sindeswar Kalan located within the Rajpura-Dariba belt in Rajasthan, NW India, have been determined. In addition, 16 carbonaceous and 2 carbonate rock samples from the ore zone have been analyzed for their Ctot and Corg contents and carbon isotope compositions. The sulfur isotope compositions range from 9.1 to –6.7 (mean value of 1.9). Increasing 34S values stratigraphically upward are observed, particularly for pyrite and pyrrhotite suggesting a syngenetic origin for the sulfur. No marked lateral isotopic variations or isotopic variation in minerals from successive laminae in banded ore samples occur. Fractionation of sulfur isotopes between coexisting sulfides suggests that the original isotopic pattern was basically preserved during the amphibolite-facies metamorphism suffered by the deposits. Corg in carbonaceous rocks ranges 0.5–9.3 wt%, with 13C values between –21 and –31 (mean of –25.4) in keeping with the biogenic derivation of the carbon. Recrystallized dolostones have 13C values close to –14.4Geological evidence and isotopic features are consistant with the following genetic scheme: (a) base-metal ores along the belt formed from geothermal emanations carrying H2S, produced by the chemical reduction of seawater sulfates and leaching of mafic volcanics, in a semiclosed (with respect to SO4), shallow-water, rift-related basin with high biological activity; (b) pyrite and pyrrhotite formed diagenetically by bacterial reduction of sulfate in pore seawater in a system open to H2S, thus bringing about the gradual enrichment of 34S in these minerals stratigraphically upward; and (c) northward in the belt, at Sindeswar Kalan, the basin of ore deposition was relatively more open. 相似文献
12.
Strata-bound sulfide deposits associated with clastic, marine sedimentary rocks, and not associated with volcanic rocks, display distributions of S34 values gradational between two extreme types: 1. a flat distribution ranging from S34 of seawater sulfate to values about 25 lower; and 2. a narrow distribution around value S34 (sulfide)=S34 (seawater sulfate) –50, and skewed to heavier values. S34 (seawater sulfate) is estimated from contemporaneous evaporites. There is a systematic relation between the type of S34 distribution and the type of depositional environment. Type 1 occurs in shallow marine or brackish-water environments; type 2 occurs characteristically in deep, euxinic basins. These distributions can be accounted for by a model involving bacterial reduction of seawater sulfate in systems which range from fully-closed batches of sulfate (type 1) to fully open systems in which fresh sulfate is introduced as reduction proceeds (type 2). The difference in the characteristic distributions requires that the magnitude of the sulfate-sulfide kinetic isotope effect on reduction be different in the two cases. This difference has already been suggested by the conflict between S34 data for modern marine sediments and laboratory experiments. The difference in isotope effects can be accounted for by Rees' (1973) model of steady-state sulfate reduction: low nutrient supply and undisturbed, stationary bacterial populations in the open system settings tend to generate larger fractionations.
Zusammenfassung Schichtgebundene Sulfid-Lagerstätten in Begleitung von klastischen, marinen Sedimentgesteinen ohne Beteiligung vulkanischer Gesteine zeigen kontinuierliche Verteilungen der S34-Werte zwischen zwei Extremtypen: 1. Eine flache Verteilung im Bereich von S34-Werten des Seewasser-Sulfats bis zu Werten, die etwa 25 niedriger liegen. 2. Eine eng begrenzte Verteilung um den S34 (Sulfid)-Wert=S34 (Seewasser-Sulfat) –50 und asymmetrischer Verteilungskurve mit stärkerer Besetzung bei den schwereren Werten. Das S34 (Seewasser-Sulfat) wird von gleichaltrigen Evaporiten abgeleitet. Es besteht eine systematische Beziehung zwischen der Art der S34-Verteilung und dem Milieu des Ablagerungsraumes. Typ 1 tritt im marinen Flachwasser oder in brackischer Umgebung auf. Typ 2 ist charakteristisch für tiefe euxinische Becken. Diese Verteilungen können erklärt werden mit Hilfe eines Modells mit bakterieller Reduktion von Meerwasser-Sulfat in Systemen, die von völlig abgeschlossenen Sulfat-Mengen (Typ 1) bis zu völlig offenen Systemen reichen, in die bei fortschreitender Reduktion frisches Sulfat zugeführt wird (Typ 2). Der Unterschied in den charakteristischen Verteilungen setzt voraus, daß die Stärke der kinetischen Sulfat-Sulfid-Isotopen-Wirkung auf die Reduktion in beiden Fällen verschieden ist. Dieser Unterschied wurde bereits wegen der Widersprüche zwischen den verschiedenen S34-Werten heutiger mariner Sedimente und Laborexperimente vermutet. Der Unterschied in der Isotopen-Wirkung kann durch das Modell von Rees (1973) für kontinuierlich ablaufende Sulfat-Reduktion erklärt werden. Geringes Nahrungsangebot und ungestörte, gleichbleibende Bakterien-Populationen in offenen Systemen neigen zur Erzeugung stärkerer Fraktionierungen.相似文献
13.
E. Pivec 《Mineralogy and Petrology》1973,19(2):87-94
Summary The studied, perfectly shaped Carlsbad twins from Loket (loc. swimming pool) are orthoclase perthites of low triclinicity (=0.0–0.3); the sodic phase relates to low albite. All phenocrysts having zonal structure contain small areas of triclinic feldspars (=0.6–0.8) independent on the zonality of low triclinicity. This microclinization is believed to be younger than the host orthoclase. The content of microcline within the phenocryst varies from about 10 to 30 percent.
With 5 Figures 相似文献
Röntgenographische, optische und chemische Variation der Kalifeldspäte von Loket (Elbogen), Karlovy Vary (Karlsbad)-Massiv, Tschechoslowakei
Zusammenfassung Die untersuchten, ideal ausgebildeten Karlsbad-Zwillinge von Loket (Lokalität Badeanstalt) sind Orthoklas-Perthite kleiner Triklinität (=0,0–0,3); die Natronfeldspat-Phase entspricht Albit. Alle Phänokristalle mit Zonarbau enthalten unabhängig von der schwachen zonaren Triklinität kleine Bereicho von triklinem Feldspat (=0,6–0,8). Diese Mikroklinisierung ist anscheinend jünger als der umschließende Orthoklas. Der Mikroklingehalt der Phänokristalle schwankt von ungefähr 10 bis zu 30%.
With 5 Figures 相似文献
14.
Mesothermal gold vein mineralization of the Samdong mine,Youngdong mining district,Republic of Korea 总被引：1，自引：0，他引：1
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
15.
Dr. T. D. Peterson Dr. S. Esperança Dr. A. N. LeCheminant 《Mineralogy and Petrology》1994,51(2-4):251-276
Summary Early Proterozoic ultrapotassic dikes, lava flows, and pyroclastic rocks of the Christopher Island Formation (CIF) erupted throughout an area 600 × 300 km within the Churchill Province of the Canadian Shield at 1.84 Ga. The rocks range from mafic lamprophyres (mg # 60; SiO2 47–54%, mean K2O/Na2O > 4) with phenocrysts of phlogopite + diopside + apatite ± olivine ± magnetite, to phenocryst-poor felsic rocks and sanidine porphyries (SiO255–69%). All samples have high incompatible element contents and display large depletions of high field strength elements relative to K, Rb, Sr, Ba, and Th. The CIF has geochemical and petrographic characteristics of both minettes and lamproites, but overall most closely resembles young Mediterranean lamproites. Felsic rocks of the CIF were produced by crystal fractionation and crustal contamination of mafic ultrapotassic magma, and include both high-silica lamproites strongly enriched in Zr, U, and Th, and weakly potassic to sodic rocks of trachytic composition. Flows and feeder dikes have relatively homogeneous Nd, 1840 Ma (–6 to –11) but highly variable ES., 1840 Ma (–40 to + 100); samples classified as lamproites have higher average Sr. Dike samples have highly variable present-day Pb isotope compositions, ranging from moderately to strongly nonradiogenic. Geochemical and isotopic data are consistent with contributions from depleted Archean lithospheric mantle, and OIB-type convecting mantle, both metasomatized by subduction-related processes during the Early Proterozoic. The lithospheric mantle probably contained Archean enriched domains as well. Proterozoic enrichment may have accompanied shallow underplating of subducted oceanic lithosphere beneath the Churchill Province during amalgamation of the Laurentian supercontinent. There are strong analogies in isotopic composition, and interpreted source region history, between the CIF and lamproites and minettes of the Wyoming Province and western Greenland, which suggest the existence of a Laurentian ultrapotassic superprovince.
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Geochemie und Entstehung der Proterozoischen ultrapotassischen Gesteine der Churchill Provinz, Kanada
Zusammenfassung Altproterozoische, ultrapotassische Gänge, Lavaströme und pyroklastische Gesteine der Christopher Island Formation (CIF), eruptierten in einem Gebiet von 600 × 300 km in der Churchill Provinz des Kanadischen Schildes vor 1.84 Ga. Die Zusammensetzung dieser Gesteine variiert von mafischen Lamprophyren (mg > 60; SiO2 = 47–54%, durchschnittliches K2O/Na2O > 4) mit Phänokristallent von Phlogopit + Diopsid + Apatit + Olivin + Magnetit, bis zu phänokristallarmen felsischen Gesteinen und Sanidinporphyren (SiO2 = 55–69%). Alle Proben zeigen hohe Gehalte an inkompatiblen Elementen und zeigen beträchtliche Verarmung an high field strength Elementen relativ zu K, Rb, Sr, Ba und Th. Die CIF hat geochemische und petrographische Eigenschaften sowohl von Minetten wie von Lamproiten, aber im allgemeinen ähnelt sie am stärksten jungen mediterranen Lamproiten. Felsische Gesteine der CIF wurden durch Fraktionierung und Krustenkontamination aus mafischen ultrapotassischen Magmen gebildet. Letztere umfassen sowohl siliziumreiche Lamproite, die deutlich an Zr, U und Th angereichert sind und schwach potassische bis sodische Gesteine von trachytischer Zusammensetzung. Lavenergüsse und zufuhrgänge zeigent ein relativ homogenes Nd, 1840 Ma (–6 bis –11) aber ein sehr variables Sr, 1840 Ma (-40 bis + 100); Proben die als Lamproite klassifiziert wurden, zeigent höhere durchschnittliche Sr-Werte. Proben von Gängen haben sehr variable Bleiisotopen-Zusammensetzungen, die von mäßig bis stark nichtradiogen variieren. Geochemische und Isotopendaten weisen auf Beiträge aus verarmtem archaischen lithosphärischen Mantel und aus konvektierendem OIB-Typ Mantel hin, die beide während des Alproterozoikums durch Subduktions-Vorgänge metasomatisiert wurden. Der lithosphärische Mantel enthielt wahrscheinlich auch angereicherte archaische Domänen. Proterozoische Anreicherungsvorgänge dürften seichtes Underplating subduzierter ozeanischer Lithosphäre unter der Churchill Provinz während der Amalgamation des laurentischen Superkontinentes begleitet haben. Es gibt starke Analogien in der Isotopenzusammensetzung und in der interpretierten Geschichte der Ursprungsregion, zwischen den CIF und Lamproiten und Minetten der Wyoming Provinz, und des westlichen Grönland. Diese weisen auf die Existenz einer laurentischen ultrapotassischen Superprovinz hin.
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16.
Four epithermal vein deposits (i.e. Dawn, Central Extended, Rose's Pride and Klondyke) in the Cracow gold field, central Queensland were investigated in terms of paragenesis, mineralogy, vein textures, fluid inclusions and stable isotopes. The Cracow epithermal field is confined to an area approximately 6 by 5 kilometers. All the deposits are hosted by the massive Camboon Andesite of Upper Carboniferous to Lower Permian age, occur as open-space vein fillings, and have similar paragenesis. However, significant variations in mineralogy, textures of quartz and adularia, and fluid geochemistry were found for a main mineralisation stage (Stage II) of each individual deposits. At Rose's Pride and Klondyke, basemetal sulphides are virtually absent, but significant amounts of calcite and quartz with minor adularia are widely distributed. Replacement textures are distinct, and mineralisation temperature is less than 220 °C and salinity less than 0.2 wt%. The
18O values of quartz and calcite range from –2.65 to –2.06 and from –6.66 to –6.34%. respectively, and calculated
18OH2O value is about –17%. which represents a nearly unshifted palaeo-meteoric water. Gold mineralisation is best developed at Central Extended among the studied deposits, where patches rich in electrum are often observed in polished thin sections and where gold grades exceeding 10 g/t are frequently indicated by assays. Base-metal sulphides are only present locally and rarely exceed 5 volume percent of the vein samples. Quartz is the dominant gangue mineral, but significant amounts of rhombic adularia and chlorite are widely distributed. Various primary and recrystallisation textures possibly inherited from silica gel are well developed and widespread. At individual sites where crustiform bands developed from both walls of a fissure, temperatures could drop sharply from 275 °C to less than 220 °C. The ore-forming fluid at Central Extended, compared with that at Rose's Pride and Klondyke, was isotopically shifted from meteoric water with
18OH2O value of –13.5 calculated in equilibrium with quartz (
18O values of –3.09 to –1.44%.). The orebodies at Dawn are rich in base-metal sulphides which are commonly coarse-grained and form up to 20 volume percent of the vein materials. Quartz is the predominant gangue mineral, and commonly shows a coarse comb texture. The ore-forming fluid was 275 ± 10 °C and low salinity (0.4 to 0.7 wt%). The
18O values of quartz range from –3.97 to –3.22%., and calculated
18OH2O value is about –12, indicating large isotopic shifts from palaeo-meteoric water. A depth zoning in typical boiling epithermal systems, corresponding to different fluid compositions, wall rock permeability and boiling behaviors, was invoked to explain different characteristics of these selected epithermal veins. 相似文献
17.
For the first time 18O and 13C values from carbonates and D values of individual n-alkanes were used to reconstruct palaeohydrological conditions in a lagoon at the southern margin of the Central European Zechstein Basin (CEZB). A 12-m core covering the complete Ca2 interval and adjacent anhydrites (A1 and A2) was analyzed for 18O and 13C values of dolomitized carbonates and D values of individual n-alkanes. 18Ocarb values (+2 to +5 vs. VPDB) were strongly influenced by evaporation and temporal freshwater input into the lagoon. The 13Ccarb values (–1 to +4 vs. VPDB) were controlled mainly by changes in primary production. Both isotopic ratios show an inverse relationship throughout most of the core, contradicting diagenetic alteration, since 13Ccarb values are not altered significantly during dolomitization. Assuming a temperature range of 35–40 °C in the lagoon, 18Ocarb values of +2.5 to +8 (vs. VSMOW) for the lagoonal water can be reconstructed. The lagoon may have desiccated twice during the Ca2 interval, as indicated by very high 18Ocarb and low 13Ccarb values, coinciding with increasing amount of anhydrite in the analyzed sample. These events seem to reflect not just local but a regional intra-Ca2 cyclicity. Measured D values of the short-chain n-alkanes, namely n-C16 and n-C18 which are widely used as indicators for photosynthetic bacterial and algal input, reflect the isotopic composition of the lagoonal water. Assuming constant fractionation during incorporation of hydrogen into lipids of –160, an average D value of +70 (vs. VSMOW) can be reconstructed for the lagoonal water, accounting for very arid conditions. The long-chain n-alkanes n-C27, n-C28, n-C29 and n-C30, thought to be derived from the leaf waxes of terrestrial higher plants, were shown to be depleted in D relative to the short-chain alkanes, therefore indicating a different hydrogen source. Terrestrial plants in arid areas mainly use water supplied by precipitation. By using a smaller fractionation of –120 due to evaporation processes in the leaves, reconstructed values vary between –74 and –9 (vs. VSMOW). These values are not indicating extremely arid conditions, implying that the long-chain n-alkanes were transported trough wind and/or rivers into the lagoon at the Zechstein Sea coast. Dwater values, reconstructed using the n-C16 alkane and 18O water values, independently reconstructed on the same sample using the temperature dependant fractionation for dolomites are good agreement and suggest high amounts of evaporation affecting the coastal lagoon. Altogether, our results indicate that hydrogen isotopic ratios of n-alkanes give information on their origin and are a useful proxy for palaeoclimatic reconstruction. 相似文献
18.
Dr. Dora Bedlivy Dr. E. J. Llambías Lic. J. F. H. Astarloa 《Mineralogy and Petrology》1972,17(2):65-75
Zusammenfassung Rooseveltit findet sich in der Oxidationszone der Lagerstätten San Francisco de los Andes und Cerro Negro de la Aguadita, in der Provinz San Juan, Argentinien, auf 30°22 S und 69°33 W. Er bildet sehr feinkörnige, weiß-graue, nach Bismuthinit pseudomorphe Aggregate. Die Brechungsindizes liegen zwischenn=2,10 und 2,30. Die Vickershärte beträgt 513 (4–5 der Mohs'schen Härteskala). Mittels Elektronenmikrosonde wurde folgende chemische Zusammensetzung bestimmt: As=21,5±1%, Bi=60,9±2%. Rooseveltit ist monoklin mita
0=6,878(1)Å, b0=7,163(1) Å, c0=6,735(1) Å, =104° 46±1, Z=4, calc.=6,94 g·cm–3, RaumgruppeP 21/n.Rooseveltit wurde nach drei verschiedenen Methoden synthetisiert. Die Pulverdiagramme der synthetischen Produkte stimmen mit dem des Minerals überein. Die Brechungsindizes wurden mitn
=2,13(2) bzw. n=2,25(2) und die Dichte mit obs.=7,01 g·cm–3 bestimmt. Zellparameter: a0-6,882(1) Å, b0=7,164(1) Å, c0=6,734(1) Å, =104° 50,5±0,7, calc.=6,94 g·cm–3. Das synthetische Material schmilzt um 950°C. Selbst nach mehrstündigem Erhitzen auf 920°C läßt sich keine Veränderung im Pulverdiagramm des Minerals festellen.Es wird versucht, die natürliche Bildung des Rooseveltits zu erklären.
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Rooseveltite from San Francisco de los Andes and Cerro Negro de la Aguadita, San Juan, Argentina
Summary Rooseveltite occurs in the weathering zone of the San Francisco de los Andes and Cerro Negro de la Aguadita mines, located in the San Juan Province, Argentina, at 30° 22S and 69° 33W. It appears in grey, finegrained aggregates pseudomorph after bismuthinite. Refraction index ranges fromn=2.10 to 2.30. The Vickers microhardness is 513 (4–5 of Mohs' scale). Chemical composition from electron micro probe measurements is As 21.5±1% and Bi 60.9±2%. Rooseveltite is monoclinic, with a0=6.878(1) Å, b0=7.163(1) Å, c0=6.735(1) Å, =104° 46±1, Z=4, calc.=6,94 g·cm–3, space groupP 21/n.The synthetic compound was prepared by three different methods. The powder pattern are the same as that of the mineral. Refraction index n=2.13(2) and n=2.25(2). The measured specific gravity is pobs.=7,01 g·cm–3. Cell parameters: a0=6.882(1) Å, b0=7.164(1) Å,c 0=6.734(1) Å, =104° 50.5±0.7, calc.=6,94 g·cm–3. The synthetic material melts at about 950°C. After heating to 920°C no variations were observed in the powder diagram of the mineral.It is tried to explain the formation of rooseveltite in natural environment.
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19.
Isotopic compositions of carbon and oxygen are studied in different (rhodochrosite, calcareous-rhodochrosite, and chlorite–rhodochrosite) types of manganese carbonate ores from the Usa deposit (Kuznetskii Alatau). The 13C value varies from –18.4 to –0.7, while the 18O value ranges between 18.4 and 23.0. Host rocks are characterized by higher values of 13C (–1.9 to 1.0) and 18O (21.2 to 24.3). The obtained isotope data suggest an active participation of oxidized organic carbon in the formation of manganese carbonates. Manganese carbonate ores of the deposit are probably related to metasomatic processes. 相似文献
20.
Ida Valeton 《Contributions to Mineralogy and Petrology》1954,4(1-2):207-216
Zusammenfassung Der primare klastische Anteil des mittleren Muschelkalks besitzt ein Maximum in den Korngrößen von 6–20, Ø , das über weite Strecken konstant bleibt. Der Mineralgehalt besteht aus Quarz, Feldspat, Glimmer und vielleieht Kaolinit.Bei der Diagenese warden Quarz und Feldspat teils korrodiert, teils wurden Quarz und Albit neu gebildet. In Randgebieten entstand Glaukonit vermutlich aus Glimmern.Durch Grundwassereinwirkung bildete rich ein zweites Maximum zwischen 0–2 Ø aus. Dabei ist in diesen Korngrößen eine Zunahme an Illit und Kaolinit und das Neuauftreten von Montmorillonit zu verzeichnen.Bei der Verwitterung verschwand das Maximum zwischen 6–20 Ø zugunsten eines Maximums zwischen 0–2 Ø . Damit verschwand auch der primäre Mineralgehalt fast völlig. Die Fraktionen unter 2 Ø setzen sich aus einem illitähnlichen Mineral zusammen.Durch Grundwassertätigkeit und Oberflächenverwitterung wurde also nicht nur der lösliche Anteil des mm ausgelaugt, sondern es sind auch deutliche Veränderungen des klastischen Anteils wahrzunehmen.Herrn Professor Dr.Carl W. Correns zum 60. Geburtstag gewidmet. 相似文献