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1.
Dalradian metamorphic rocks, Lower Ordovician meta-igneous rocks (MGS) and Caledonian granites of the Connemara complex in SW Connemara all show intense retrograde alteration. Alteration primarily involves sericitization and saussuritization of plagioclase, the alteration of biotite and hornblende to chlorite and the formation of secondary epidote. The alteration is associated with sealed microcracks in all rocks and planes of secondary fluid inclusions in quartz where it occurs, and was the result of a phase of fluid influx into these rocks. In hand specimen K-feldspar becomes progressively reddened with increasing alteration. Mineralogical alteration in the MGS and Caledonian granites took place at temperatures 275±15°C and in the MGS Pfluid is estimated to be 1.5 kbar during alteration. The °D values of alteration phases are:-18 to-29 (fluid inclusions),-47 to-61 (chlorites) and-11 to-31 (epidotes). Chlorite 18O values are +0.2 to +4.3, while 18O values for quartz-K-feldspar pairs show both positively sloped (MGS) and highly unusual negatively sloped (Caledonian granites) arrays, diverging from the normal magmatic field on a - plot. The stable isotope data show that the fluid that caused retrogression continued to be present in most rocks until temperatures fell to 200–140°C. The retrograde fluid had D -20 to-30 in all lithologies, but the fluid 18O varied both spatially and temporally within the range-4 to +7. The fO2 of the fluid that deposited the epidotes in the MGS varied with its 18O value, with the most 18O-depleted fluid being the most oxidizing. The D values, together with low (<0) 18O values for the retrograde fluid in some lithologies indicate that this fluid was of meteoric origin. This meteoric fluid was probably responsible for the alteration in all lithologies during a single phase of fluid infiltration. The variation in retrograde fluid 18O values is attributed to the effects of variable oxygen isotope shifting of this meteoric fluid by fluid-rock interaction. Infiltration of meteoric fluid into this area was most likely accomplished by convection of pore fluids around the heat anomaly of the Galway granite soon after intrusion at 400 Ma. However convective circulation of meteoric water and mineralogical alteration could possible have occurred considerably later.  相似文献   

2.
The Jurassic Notch Peak granitic stock, western Utah, discordantly intrudes Cambrian interbedded pure limestones and calcareous argillites. Contact metamorphosed argillite and limestone samples, collected along traverses away from the intrusion, were analyzed for 18O, 13C, and D. The 13C and 18O values for the limestones remain constant at about 0.5 (PDB) and 20 (SMOW), respectively, with increasing metamorphic grade. The whole rock 18O values of the argillites systematically decrease from 19 to as low as 8.1, and the 13C values of the carbonate fraction from 0.5 to –11.8. The change in 13C values can be explained by Rayleigh decarbonation during calcsilicate reactions, where calculated is about 4.5 permil for the high-grade samples and less for medium and low-grade samples suggesting a range in temperatures at which most decarbonation occurred. However, the amount of CO2 released was not anough to decrease the whole rock 18O to the values observed in the argillites. The low 18O values close to the intrusion suggest interaction with magmatic water that had a 18O value of 8.5. The extreme lowering of 13C by fractional devolatilization and the lowering of 18O in argillites close to the intrusion indicates oxgen-equivalent fluid/rock ratios in excess of 1.0 and X(CO2)F of the fluid less than 0.2. Mineral assemblages in conjunction with the isotopic data indicate a strong influence of water infiltration on the reaction relations in the argillites and separate fluid and thermal fronts moving thru the argillites. The different stable isotope relations in limestones and argillites attest to the importance of decarbonation in the enhancement of permeability. The flow of fluids was confined to the argillite beds (argillite aquifers) whereas the limestones prevented vertical fluid flow and convective cooling of the stock.  相似文献   

3.
The Myall Creek copper prospect is in unmetamorphosed carbonaceous dolosiltstone and sandstone at the base of the late Proterozoic (Adelaidean) Tapley Hill Formation. It contains disseminated, fine-grained chalcopyrite, zincian tennanite, bornite, chalcocite, pyrite, sphalerite and galena, and irregular to straight chalcopyrite-rich veinlets. Some ore minerals rim and/or partially replace pyrite or clastic grains. There is no evidence of hydrothermal activity. The 34SCDT values of pyrite and the other sulfides fall in the wide range –3.6 to +44.2. Dolomite in both mineralised and unmineralised samples has 13CPDB values concentrated around –3, and 18OSMOW values around +25. It is concluded that the mineralising fluids were near-neutral brines which leached metals from the basement and early Adelaidean rocks. They entered the Tapley Hill sediments at moderately low temperatures via permeable strata and faults. The metals were precipitated by biogenic H2S, and also fixed by reaction with iron sulfides and, possibly, organic matter. Continuing ascent of brines into the mineralised strata caused breakdown of detrital feldspars and Fe-Ti oxides, and some solution-remobilisation of early-formed sulfides.  相似文献   

4.
The world-class Idrija mercury deposit (western Slovenia) is hosted by highly deformed Permocarboniferous to Middle Triassic sedimentary rocks within a complex tectonic structure at the transition between the External Dinarides and the Southern Alps. Concordant and discordant mineralization formed concomitant with Middle Triassic bimodal volcanism in an aborted rift. A multiple isotopic (C, O, S) investigation of host rocks and ore minerals was performed to put constraints on the source and composition of the fluid, and the hydrothermal alteration. The distributions of the 13C and 18O values of host and gangue carbonates are indicative of a fracture-controlled hydrothermal system, with locally high fluid-rock ratios. Quantitative modeling of the 13C and 18O covariation for host carbonates during temperature dependent fluid-rock interaction, and concomitant precipitation of void-filling dolomites points to a slightly acidic hydrothermal fluid (13C–4 and 18O+10), which most likely evolved during isotopic exchange with carbonates under low fluid/rock ratios. The 34S values of hydrothermal and sedimentary sulfur minerals were used to re-evaluate the previously proposed magmatic and evaporitic sulfur sources for the mineralization, and to assess the importance of other possible sulfur sources such as the contemporaneous seawater sulfate, sedimentary pyrite, and organic sulfur compounds. The 34S values of the sulfides show a large variation at deposit down to hand-specimen scale. They range for cinnabar and pyrite from –19.1 to +22.8, and from –22.4 to +59.6, respectively, suggesting mixing of sulfur from different sources. The peak of 34S values of cinnabar and pyrite close to 0 is compatible with ore sulfur derived dominantly from a magmatic fluid and/or from hydrothermal leaching of basement rocks. The similar stratigraphic trends of the 34S values of both cinnabar and pyrite suggest a minor contribution of sedimentary sulfur (pyrite and organic sulfur) to the ore formation. Some of the positive 34S values are probably derived from thermochemical reduction of evaporitic and contemporaneous seawater sulfates.Editorial handling: P. Lattanzi  相似文献   

5.
Kuroko-type massive sulfide deposits of the Eastern Black Sea province of Turkey are related to the Upper Cretaceous felsic lavas and pyroclastic rocks, and associated with clay and carbonate alteration zones in the footwall and hangingwall lithologies. A complete upward-vertical section of a typical orebody consists of a stringer-disseminated sulfide zone composed mainly of pyrite and chalcopyrite; a massive pyrite zone; a massive yellow ore consisting mainly of chalcopyrite and pyrite; a black ore made up mainly of galena and sphalerite with minor amounts of chalcopyrite, bornite, pyrite and various sulfosalts; and a barite zone. Most of the deposits in the province are associated with gypsum in the footwall or hangingwall. The paragenetic sequence in the massive ore is pyrite, sphalerite, chalcopyrite, bornite, galena and various sulfosalts, with some overlap between the mineral phases. Massive, stringer and disseminated sulfides from eight kuroko-type VMS deposits of the Eastern Black Sea province have a 34S range of 0–7 per mil, consistent with the 34S range of felsic igneous rocks. Sulfides in the massive ore at Madenköy (4.3–6.1 per mil) differ isotopically from sulfides in the stringer zone (6.3–7.2 per mil) suggesting a slightly increased input of H2S derived from marine sulfate with time. Barite and coarse-grained gypsum have a 34S range of 17.7–21.5 per mil, a few per mil higher than the 34S value of contemporaneous seawater sulfate. The deposits may, therefore, have formed in restricted basins in which bacterial reduction of sulfate was taking place. Fine-grained, disseminated gypsum at Kutlular and Tunca has 34S values (2.6–6.1 per mil) overlapping those of ore sulfides, indicating sulfide oxidation during waning stages of hydrothermal activity.  相似文献   

6.
This paper deals with barite from stratiform, karst, and vein deposits hosted within Lower Paleozoic rocks of the Iglesiente-Sulcis mining district in southwestern Sardinia. For comparison sulfates from mine waters are studied. Stratiform barite displays 34S=28.8–32.1, 18O=12.7–15.6, and 87Sr/86Sr=0.7087, in keeping with an essentially Cambrian marine origin of both sulfate and strontium. Epigenetic barite from post-Hercynian karst and vein deposits is indistinguishable for both sulfur and oxygen isotopes with 34S=15.3–26.4 and 18O=6.6–12.5; 87Sr/86Sr ratios vary 0.7094–0.7140. These results and the microthermometric and salinity data from fluid inclusions concur in suggesting that barite formed at the site of mineralization by oxidation of reduced sulfur from Cambrian-Ordovician sulfide ores in warm, sometimes hot solutions consisting of dilute water and saline brine with different 18O values. The relative proportion of the two types of water may have largely varied within a given deposit during the mineralization. In the karst barite Sr was essentially provided by carbonate host rocks, whereas both carbonate and Lower Paleozoic shale host rocks should have been important sources for Sr of the vein barite. Finally, 34S data of dissolved sulfate provide further support for the mixed seawater-meteoric water composition of mine waters from the Iglesiente area.  相似文献   

7.
New sulphur and sulphate-oxygen isotope measurements for the main discordant and stratiform lead-zinc-barite orebodies at Silvermines Co. Tipperary, allow reappraisal of previously offered differing interpretations (Graham, 1970; Greig et al., 1971) of the bearing of sulphur isotopes on the genesis of this important Irish deposit. The following aspects of the data are confirmed: barite 34 S-values range from 17–21, similar to lower Carboniferous seawater sulphate: stratiform sulphide lens pyrites have 34 S-values ranging from –13 to –36; vein sulphide 34 S-values range from –8 to 4; sulphide 34 S-values increase upwards and outwards respectively in the related discordant and stratiform G orebodies; galena-sphalerite isotope palaeotemperatures are not too consistent, ranging from 40 to 430°C (using the calibration of Czamanske and Rye (1974). New facts are as follows: barite 18O-values range from –13 to –17, stratiform barites ranging from 13 to 14.5; sulphides separated from a single stratiform ore lens hand specimen usually have 34 Ssl > 34 Sga > 34 Spy; the outward decrease in 34 S-values in the stratiform G orebody is confined to the first few hundred feet only; pyrite 34 S-values progressively increase downwards through one stratiform sulphide orebody; yet variations of 13 occur within a single colloform pyrite structure from another stratiform orebody. It is concluded that there were at least two sources of sulphur, seawater sulphate and deep-seated sulphur. The former was the dominant source of all sulphate and, via biogenic reduction, of the sulphur in the bulk of the stratiform sulphide. The latter was the source of the sulphur in the vein sulphides. There was minimal isotopic interaction between the cool seawater sulphate and the warm unwelling ore fluid sulphur species, even though the latter precipitated under near isotopic equilibrium conditions when the temperature dropped and/or the pH and Eh increased. The lack of isotopic equilibrium between pyrite and ore sulphides in the stratiform ore lenses may result from the latter having precipitated slightly later than the former because of solubility relationships. Overall the present isotopic evidence supports considerable geological evidence favoring a syngenetic origin for the stratiform Silvermines orebodies.  相似文献   

8.
Oxygen and hydrogen isotope studies of a number of granite suites and mineral separates from the New England Batholith indicate that O18 can be used to discriminate the major granite protoliths. The granite suites previously subdivided on the basis of mineralogical and geochemical criteria into S-type (sedimentary) and I-type (igneous) have O18 values consistently higher in the S-type granites (10.4–12.5) than in the spatially related I-type plutons (7.7–9.9). There appears to be a systematic variation in O18 from the most S-type to the most I-type granites, the dividing point between the two occuring at O18 equal to 10. A group of leucocratic granites that form about half of the batholith and difficult to classify mineralogically and geochemically is found to have low O18 values (6.4–8.1), suggesting an affinity to the most I-type granites. A single leucogranite pluton with minor muscovite has a O18 of 9.6 which is significantly higher than other leucogranites indicating a different origin perhaps involving amphibole fractionation.The behavior of D in the plutonic rocks is much less systematic than O18. Excluding samples collected adjacent to major faults, the D values show a rough positive correlation with water content similar to, but less pronounced than, the trend previously observed in the Berridale Batholith, southeastern Australia. This relation is considered to reflect an interaction between meteoric water and the granites, the largest effect being observed in samples with the least amount of water. Of note is the generally lower D values of the upper Paleozoic New England Batholith compared with the Silurian Berridale Batholith. This difference may be related to a near equatorial paleolatitude of 22 °S in the Silurian and near polar paleolatitudes in the late Carboniferous that have been inferred for these regions. Granite samples collected from near major faults, and one ignimbrite sample of rhyodacite composition, have very low D values (less than –120) suggesting a much greater degree of interaction with meteoric water.  相似文献   

9.
Stable isotope data have been determined for 13 Mesozoic and Tertiary plutons in eastern Nevada and nearby Utah. In the southern Snake Range of eastern Nevada, where relations are best exposed and have been most intensively studied, D, 18O, and apparent K-Ar ages depend on proximity to the Snake Range decollement. Where stresses resulting from late movement on the decollement have caused cataclasis of Oligocene (37 Ma) granitoid rock, 18O, D, and K-Ar age values as low as –2.5, –155, and 18 Ma, respectively, have been determined. Where there has been no cataclasis, 18O values of Jurassic, Cretaceous, and Oligocene granitoid rocks are apparently unaffected, but both D values and K-Ar ages have been modified for distances of tens of meters below the decollement.Results similar to those in the southern Snake Range have been observed in other eastern Nevada granitoid rocks spatially related to regional thrust faults, as in the Kern Mountains, the Toana Range, and the northern Egan Range. In each of these areas cataclasis or deformation of granitoid rocks has resulted in lowered 18O, D, and K-Ar age values. Where there has been no cataclasis or deformation, 18O values are unaffected, but both D and K-Ar age values have been lowered by stresses resulting from postcrystallization movement along overlying thrust faults.Many of the plutons discussed have not been deeply eroded, and spatially related thrust faults crop out. Where thrust faults are not in evidence and the granitoid rocks give D values lower than about –130 along with spuriously low K-Ar age results, modification of the D and K-Ar age values may have been caused by stresses related to late movement along an overlying (now eroded) thrust fault.  相似文献   

10.
Sulphur isotopic compositions of sulphides within garnet-rich rocks and high-grade ore from the Broken Hill deposit, New South Wales, Australia, have been determined and show a range of values of –3.3 to +6.7 per mil. Thermochemical considerations, including the spread of values of 34S, suggest that the deposit was derived from a mixed source of sulphur in which seawater, reduced by inorganic processes, mixed with magmatic sulphur or that sulphate from contemporaneous seawater was reduced biogenically at low temperatures. Thermochemical considerations also suggest that pyrrhotite formed by desulphidation of pyrite so that the original Fe-S-O assemblage was pyrite ± magnetite.34S measurements show a broad range which is considered to be due to isotopic reequilibration during retrograde metamorphism and analytical and sampling technique. These data should not be used to indicate original temperatures of deposition or metamorphic temperatures associated with the various metamorphic events.  相似文献   

11.
Sulfur isotope ratios have been determined in 27 selected volcanic rocks from Iceland together with their whole rock chemistry. The 34S of analyzed basalts ranges from –2.0 to +0.4 with an average value of –0.8 Tholeiitic and alkaline rocks exhibit little difference in 34S values but the intermediate and acid rocks analyzed have higher 34S values up to +4.2 It is suggested that the overall variation in sulfur isotope composition of the basalts is caused by degassing. The small range of the 34S values and its similarity to other oceanic and continental basalts, suggest that the depleted mantle is homogeneous in its sulfur isotope composition. The 34S of the depleted mantle is estimated to be within the range for undegassed oceanic basalts, –0.5 to +1.0  相似文献   

12.
The oxygen isotope geochemistry and chemical composition of clinopyroxene crystals from Alban Hills pyroclastic deposits constrain the petrological evolution of ultrapotassic Roman-type rocks. Volcanic eruptions in the 560–35 ka time interval produced thick pyroclastic deposits bearing clinopyroxene phenocrysts with recurrent chemical characteristics. Clinopyroxenes vary from Si–Mg-rich to Al–Fe-rich with no compositional break, indicating that they were derived from a continuous process of crystal fractionation. Based on the 18O and trace element data no primitive samples were recovered: monomineralic clinopyroxene cumulates set the oxygen isotope composition of primary magmas in the range of uncontaminated mantle rocks (5.5), but their REE composition resulted from extensive crystal fractionation. Departing from these mantle-like 18OCpx values the effects of crustal contamination of clinopyroxene O-isotope composition were identified and used to monitor chemical variations in the parental magma. 18O values in Si–Mg-rich clinopyroxene are slightly higher than typical mantle values (5.9–6.2), and the low REE contents are representative of early stages of magmatic differentiation. 18O values as high as 8.2 are associated with Al–Fe3+-rich clinopyroxene showing high REE contents. These 18O values are characteristic of crystals formed during the late magmatic stages of each main eruptive phase. Geochemical modelling of 18O values vs. trace element contents indicates that these ultrapotassic magmas were derived from fractional crystallization plus assimilation of limited amounts of carbonate wall rocks starting from a primary melt, and from interaction with CO2 derived from country rocks during crystal fractionation.  相似文献   

13.
Oxygen and carbon isotope compositions were determined for calcites from the Green Tuff formations of Miocene age in Japan. Values of 18O from 24 calcites in altered rocks from 5 districts range from –2 to +16SMOW, in most cases from 0 to +8SMOW. The low 18O values rule out the possibility of their low-temperature origin or any significant contribution of magmatic fluid in the calcite precipitation. These values, coupled with their mineral assemblages, suggest that the calcites formed from meteoric hydrothermal solutions which caused propylitic alteration after the submarine strata became emergent.Values of 13C from the calcites show a wide variation from –17 to 0PDB. Calcites from different districts have different ranges of 13C values, indicating that there was no homogeneous reservoir of carbon at the time the calcite formed, and that the carbon had local sources. Carbon isotopic compositions of calcite within ore deposits in the Green Tuff formations range from –19 to 0PDB, similar to those of calcite in the altered rocks in the same district, suggesting that the carbon in ore calcites was likely supplied from the surrounding rocks through activity of meteoric hydrothermal solutions.  相似文献   

14.
Summary The stable isotope geochemistry of native gold-bearing quartz veins contained within low-grade metasedimentary strata in the central Canadian Rocky Mountains, British Columbia is examined. The data augment previous geological and geochemical studies.Vein pyrite 34S values cluster between + 14.2 and + 16.3 (CDT). Coeval galenas exhibit 34S values between + 11.4 and 13.3. Pyrite-galena geothermometry reveals a mean temperature of mineralization of 300 ± 43°C. Comparison of 34S values for the vein pyrites, with values for pyrite porphyroblasts in country rocks suggests that vein sulfur was probably derived from the host rocks.18O(SMOW) values of host quartzites and pelites cluster between + 12.0 and + 13.5, and + 9.5 and + 10.5, respectively. Auriferous vein quartz exhibits 18O values between + 13.0 and + 15.0. Veins were likely deposited from fluids undergoing post-peak metamorphic cooling.Vein inclusion fluids exhibit values between –105 and –124 (SMOW). Combined O-H-isotope data are most compatible with a source fluid involving chemically- and isotopically-evolved meteoric waters.The critical role of H-isotope data in the evaluation of source fluids for such mesothermal gold lodes is stressed. The paucity of H-isotope data pertaining to the study of lode gold deposits in similar low-grade metasedimentary domains suggests that the involvement of meteoric waters may at times be overlooked.
Der Ursprung metamorphogener Gold-Ganglagerstätten: Bedeutung stabiler Isotopendaten aus den zentralen Rocky Mountains, Kanada
Zusammenfassung Die vorliegende Arbeit befaßt sich mit der Untersuchung der Geochemie stabiler Isotope goldführender Quarzgänge in schwach metamorphen Sedimenten der zentralen Rocky Mountains in Britisch Kolumbien, Kanada. Die Resultate ergänzen früher publizierte geologische und geochemische Daten.Die 34S-Werte von Gang-Pyrit liegen zwischen + 14.2 und + 16.3 (CDT); gleichzeitig gebildeter Bleiglanz hat 34S-Werte von + 11.4 bis + 13.3. Die Isotopengeothermo metrie des Pyrits und Bleiglanzes ergibt eine mittlere Mineralisationstemperatur von 300°C + 43° für diese beiden Minerale. Vergleiche der 8345-Werte des Gang-Pyrits mit denen von Pyrit-Porphyroblasten des Nebengesteins lassen für die Gang-Pyrite eine Herkunft des Schwefels aus dem Nebengestein als wahrscheinlich erscheinen.Die 18O-Werte von Quarziten und Peliten, die als Nebengesteine auftreten, streuen von + 12.0 bis + 13.5 (SMOW), beziehungweise von +9.5 bis + 10.5 Quarz goldführender Gänge hat 18O-Werte, die zwischen + 13.0 und + 15.0 (SMOW) liegen. Er wurde als Gangfüllung wahrscheinlich bei sinkenden Temperaturen aus post metamorphen wäßrigen Lösungen abgesetzt.Flüssigkeitseinschlüsse von Gangmineralien zeigen D-Werte von -105 bis -124 (SMOW). Die H-O-Isotope sind deshalb ein Hinweis dafür, daß als mineralisierende Lösungen isotopisch veränderte meteorische Wässer in Betracht zu ziehen sind. Bei der Deutung der Herkunft der mineralisierenden wäßrigen Lösungen von mesothermalen Goldgängen muß die Kenntnis der H-Isotope als kritisch betrachtet werden. Die Seltenheit mit der H-Isotopendaten dieses Lagerstättentyps in der Literatur diskutiert werden, dürfte ein wesentlicher Grund dafür sein, daß die Rolle meteorischer Wässer bei der Genese mesothermaler, in Metasedimenten liegender Goldgänge, vielfach übersehen wurde.

With 4 Figures  相似文献   

15.
Summary The Ambadungar (Amba Dongar) alkaline carbonatite complex is emplaced in the Deccan traps igneous province. A wide range of carbonatites and alkaline rocks are exposed around Ambadungar. The alkaline rocks have been classified as tinguaite, phonolite and/or phononephelinite, melanephelinite, and syenite and/or nepheline syenite whereas carbonatites vary from calcio-carbonatites to ferro- and silicocarbonatites. The enrichment in large-ion lithophile elements (LILE), P, and rare-earth elements (REE) in carbonatites is considered to result from fractionation of a mantle derived magmatic liquid, i.e. nephelinitic magma, by liquid immiscibility which also produced melanephelinite and/or phononephelinite with high field strength elements (HFSE) such as Ca, Mg, Fe, and Mn in the alkaline silicate liquid fraction. The La:Lu ratios of the carbonatites are typical of igneous rocks and vary between 590 and 1945, similar to many known magmatic carbonatites. The 13C concentration varies between –2 and –8 whereas 18O-values vary between 7.7 and 26.8. The 13C concentration is typical of primary igneous carbonatites but 18O enrichment is thought to be the result of post-magmatic processes such as interaction with meteoric water and re-equilibration with hydrous fluids at low temperatures.
Petrologie, Geochemie und Genese der riftgebundenen Karbonatite von Ambadungar, Indien
Zusammenfassung Der Ambadungar (Amba Dongar) Alkalikarbonatit-Komplex liegt in der magmatischen Deccan Provinz. Er umfaßt eine Vielzahl von karbonatitischen und alkalischen Gesteinen, die in der Umgebung von Ambadungar aufgeschlossen sind. Die Alkaligesteine sind als Tinguaite, Phonolite und/oder Phononephelinite, Melanephelinite, Syenite und/oder Nephelinsyenite zu klassifizieren, die Karbonatite als Calcio-, bis Ferro- and Silicokarbonatite. Die Anreicherung an LIL-Elementen und Seltenen Erden in den Karbonatiten werden als das Ergebnis der Fraktionierung von Mantelschmelzen, i.e. eines nephelinitisches Magmas, infolge von Nichtmischbarkeit interpretiert. Melanephelinite und/oder Phononephelinite and hohe Gehalte an HFS-Elementen (Ca, Mg, Fe and Mn) in der alkalisch-silikatischen Schmelzfraktion sind ebenfalls das Ergebnis dieser Prozesse. Die La/Lu-Verhältnisse sind typisch für magmatische Karbonatite and variieren zwischen 590 and 1945. Die 13C Konzentrationen variieren zwischen -2 and -8 %o, die 18O Werte zwischen 7.7 and 26.8 %0. Während die 13C Konzentration typisch für primär magmatische Karbonatite ist, ist die 18O-Anreicherung mit postmagmatischen Prozessen, wie etwa die Interaktion mit meteorischen Wässern and die Reequilibration mit niedrig temperierten wäßrigen Fluiden, erklärbar.

with 11 figures  相似文献   

16.
Previous studies of galena and sphalerite from Paleozoic MVT deposits in the Viburnum Trend, southeast Missouri documented large variations in 34S values throughout the ore-forming event. The present study of Cu-Fe-sulfides reveals a similar 34S variation that reflects two end-member sulfur reservoirs whose relative importance varied both temporally and spatially. More 34S-enriched sulfides (34S approaching 25) indicate introduction of sulfur from basinal sedimentary sources, whereas more 32S-enriched sulfides (34S < 5) may reflect fluids moving through underlying granitic basement. Two areas containing Precambrian, igneous-hosted FeCu mineralization in southeast Missouri (West and Central Domes of Boss-Bixby) were investigated to elucidate their relationship to Cu-rich MVT orebodies hosted nearby within the overlying Cambrian Bonneterre Dolomite. Mineralization at Boss-Bixby is composed of an early phase of iron oxide deposition followed by Cu-Fe-sulfides. The Central Dome is faulted and its mineralization is more fracture-controlled than the typically podiform ores of the West Dome. The 34S values of West Dome sulfides are 0.9 to 6.5 and pyrite-chalcopyrite indicate a temperature of 525° ± 50 °C. These data indicate an igneous source of sulfur during Precambrian ore deposition. In contrast, 34S values of Central Dome sulfides are 9.4 to 20.0 and pyrite-chalcopyrite indicate temperatures of 275° ± 50 °C. Similar 34S values are obtained for chalcopyrite from the overlying MVT deposits. We speculate that deeply circulating, basin-derived MVT fluids mobilized sulfur and copper from the underlying igneous basement and redeposited them in overlying Curich MVT orebodies, as well as overprinting earlier Precambrian sulfides of the Central Dome with a later, Paleozoic MVT sulfur isotope signature. Many models for MVT fluid circulation in the Midcontinent region of North America assume that igneous basement rocks are an impermeable boundary, but in southeast Missouri, evidence exists for structurally controlled MVT fluid movement > 600 m vertically through underlying Precambrian igneous rocks. Such basement involvement has been suggested for other carbonate-hosted base-metal districts (e.g. Irish base metal deposits) and should be considered an integral part of the ore-forming process in southeast Missouri.  相似文献   

17.
Sulfur isotope analyses were made on 14 alunites from volcanic and sedimentary rocks widely different in chemistry and age from southern Tuscany and northern Latium, central Italy. The 34S values range from +0.7 to +9.6, and appear not to be related to the nature of the host rock. Geological and isotopic evidence suggests that all the alunites formed by supergenic oxidation of sulfides. Sulfides occurring with alunites in the volcanic rocks of Latium can be divided into an isotopically light group of probably magmatic origin (34S=–1.5 to +3.4) and a heavy one with 34S=+6.0 to +10.3, tentatively interpreted as deposited by hydrothermal fluids that leached sulfides of similar 34S/32S from the deep basement. Such an interpretation is consistent with recent studies indicating that in the perityrrhenian belt of Latium exists a continuation, at depth, of the Tuscan stratigraphic series, rich in sulfides with 34 from +6 to +12.  相似文献   

18.
Oxygen-isotope compositions have been measured for whole-rock and mineral samples of host and hydrothermally altered rocks from three massive sulfide deposits, Centennial (CL), Spruce Point (SP), and Anderson Lake (AL), in the Flin Flon — Snow Lake belt, Manitoba. Wholerock 18O values of felsic metavolcanic, host rocks (+8.5 to +16.1) are higher than those of altered rocks from the three deposits. The 18O values of altered rocks are lower in the chlorite zone and muscovite zone-I (CL=+ 5.3; SP=+5.4 to +8.3; AL= +3.7 to +5.9) than in the gradational zone (CL= +9.9 to +11.7; SP= +8.4 to +9.8; AL= + 6.6 to +7.7). Muscovite schist (Muscovite Zone-II) enveloping the Anderson Lake ore body has 18O values of +7.2 to +8.3. Quartz, biotite, muscovite, and chlorite separated from the altered rocks have lower 18O values compared to the same minerals separated from the host rocks. However, isotopic fractionation between mineral-pairs is generally similar in both host and altered rocks.It is interpreted that differences in the oxygen-isotope compositions of the altered and host rocks were produced prior to metamorphism, during hydrothermal alteration related to ore-deposition. Isotopic homogenization during metamorphism occurred on a grain-to-grain scale, over no more than a few meters. The whole-rock 18O values did not change significantly during metamorphism. The generally lower 18O values of altered rocks, the Cu-rich nature of the ore and the occurrence of the muscovite zone-II at Anderson Lake are consistent with the presence of higher temperature hydrothermal fluids at Anderson Lake than at the Centennial and Spruce Point deposits.  相似文献   

19.
Isotopic compositions were determined for quartz, sericite and bulk rock samples surrounding the Uwamuki no. 4 Kuroko ore body, Kosaka, Japan. 18O values of quartz from Siliceous Ore (S.O.), main body of Black Ore B.O.) and the upper layer of B.O. are fairly uniform, +8.7 to +10.5. Formation temperatures calculated from fractionation of 18O between sericite and quartz from B.O. and upper S.O. are 250° to 300° C. The ore-forming fluids had 18O values of +1 and D values of –10, from isotope compositions of quartz and sericite.Tertiary volcanic rocks surrounding the ore deposits at Kosaka have uniform 18O values, +8.1±1.0 (n=50), although their bulk chemical compositions are widely varied because of different degrees of alteration. White Rhyolite, which is an intensely altered rhyolite occurring in close association with the Kuroko ore bodies, has also uniform 18O values, +7.9±0.9 (n=19). Temperatures of alteration are estimated to be around 300° C from the oxygen isotope fractionation between quartz and sericite. Paleozoic basement rocks phyllite and chert, have high 18O values, +18 and +19. The Sasahata formation of unknown age, which lies between Tertiary and Paleozoic formations, has highly variable 18O, +8 to +16 (n=4). High 18O values of the basement rocks and the sharp difference in 18O at their boundary suggest that the hydrothermal system causing Kuroko mineralization was mainly confined within permeable Tertiary rocks. D values of altered Tertiary volcanic rocks are highly variable ranging from –34 to –64% (n=12). The variation of D does not correlate with change of chemical composition, 18O values, nor distance from the ore deposits. The relatively high D values of the altered rocks indicate that the major constituent of the hydrothermal fluid was sea water. However, another fluid having lower D must have also participated. The fluid could be evolved sea water modified by interaction with rocks and the admixture of magmatic fluid. The variation in D may suggest that sea water mixed dispersively with the fluid.  相似文献   

20.
Kyser, O'Neil, and Carmichael (1981, 1982) measured the 18O values of coexisting minerals from peridotite nodules in alkali basalts and kimberlites, interpreting the nodules as equilibrium assemblages. Based mainly on the systematics revealed in 18O-olivinevs. 18O-pyroxene diagrams, we have re-interpreted the Kyser et al. data as non-equilibrium phenomena. On such- diagrams, the mantle nodules exhibit data arrays that cut across the 18O=zero line; these arrays strongly resemble the non-equilibrium quartz-feldspar and feldspar-pyroxene 18O arrays that we now know arediagnostic of hydrothermally altered plutonic igneous rocks. Thus, the peridotites appear to have been open systems that underwent metasomatic exchange with an external, oxygen-bearing fluid (CO2 magma, H2O, etc.); during this event, the relatively inert pyroxenes exchanged at a much slower rate than did the coexisting olivines and spinels. This accounts for the correlation between 18O pyroxene-olivine and the whole-rock 18O of the peridotites, which is a major difficulty with the equilibrium interpretation. The metasomatic18O-enrichments of the peridotites can be related to metasomatic enrichments in LIL elements and the development of amphibole and phlogopite. This type of precursor metasomatic activity can explain the development of alkali basalt magmas, as well as leucitites and nephelinites (all of which tend to be slightly18O-rich relative to MORB, with 18O=+6 to +7.5). Fluids with appropriate 18O values to explain the open-system metasomatic effects can be produced by exchange with ancient subducted oceanic crust (eclogite). However, fluid/rock ratios of about 0.4 to 2.5 are required, indicating that this cannot be a mantle-wide phenomenon. Also, these non-equilibrium effects are apparently transient phenomena, probably associated with the eruptive events that brought the nodules to the surface; at characteristic mantle temperatures, the effects would likely disappear in a few tens of millions of years, or less, implying that the ultramafic nodules are not typical samples of the upper mantle.Contribution No. 4156, Publications of the Division of Geological and Planetary Sciences, California Institute of Technology  相似文献   

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