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1.
Abstract. Talnakhite occurs in an andradite skarn forming adjacent to a leucocratic quartz monzonite dike intruded into limestone at Fuka. The mineral densely contains exsolution lamellae of chalcopyrite, and the talnakhite-chalcopyrite inter-growth is intimately associated with bornite that contains chalcopyrite as a lattice-form exsolution. The chemical composition of the talnakhite acquired on an electron probe microanalyzer corresponds to Cu9.00 Fe8.08 S15.92 , very close to the ideal chemical formula Cu9 Fe8 S16 . Nickel is not detected. The X-ray powder diffraction lines are well indexed on a body-centered cubic cell with a = 10.589 Å. The characteristic (110) reflection of talnakhite is clearly observed at 7.49 Å. The present talnakhite retains the chalcopyrite-like colored polished surface without tarnish in air more than a month.
Talnakhite at Fuka is likely to be derived from breakdown of Cu-rich intermediate solid solution ( iss ), which was in equilibrium with Fe-rich bornite at elevated temperatures. Talnakhite thus formed has survived the subsequent cooling processes, probably because the ƒs 2 was maintained in suitable levels preventing its decomposition into bornite and chalcopyrite. 相似文献
Talnakhite at Fuka is likely to be derived from breakdown of Cu-rich intermediate solid solution ( iss ), which was in equilibrium with Fe-rich bornite at elevated temperatures. Talnakhite thus formed has survived the subsequent cooling processes, probably because the ƒ
2.
On the Occurrence of Silician Magnetites 总被引：2，自引：0，他引：2
Hidehiko Shimazaki 《Resource Geology》1998,48(1):23-29
Abstract: About 120 specimens of magnetite from various localities are examined by an electron microprobe analyzer. Magnetites containing more than one weight percent of silica but lack of any other components than ferrous and ferric iron, called silician magnetites in the present paper, are recognized in 23 skarn, one vein and one thermally metamorphosed massive sulfide deposits. Thus it is confirmed that this mineral occurs in nature much more frequently than so far expected. Besides silician magnetites, magnetites with appreciable amounts of Al2 O3 , CaO, MgO and other components along with silica, are also recognized in some skarn deposits. Magnetites with such unusual compositions are found only in hydrothermal environments, and it is suggested that precipitation mechanisms seem to be responsible for their formation.
In silician magnetites, excess electric charge brought by the replacement of ferric iron in tetrahedral site by silicon, could be compensated by the replacement of ferric iron in octahedral site by ferrous iron, known as γ–Fe2 SiO4 component. The natural occurrence of silician magnetites, however, gives no positive support to the existence of this component at crustal pressures. Instead a preliminary Mössbauer experiment demonstrates that one silician magnetite has a maghemite –like structure by the omission of ferrous iron from octahedral site. 相似文献
In silician magnetites, excess electric charge brought by the replacement of ferric iron in tetrahedral site by silicon, could be compensated by the replacement of ferric iron in octahedral site by ferrous iron, known as γ–Fe
3.
Abstract Microprobe analysis of the continuous chemical evolution of coexisting biotite-garnet and biotite-garnet-staurolite has been undertaken from interbedded micaschists of the volcanodetrital group of the Vilaine. A thermobarometric study using pertinent mineralogical equilibria reveals a complex P-T evolution, continuous throughout time, from high pressure, medium temperature (kyanite zone) to medium pressure, high temperature (sillimanite zone), then low pressure, medium temperature (andalusite zone). The T, P, fH 2 o and XH 2 o variations have been calculated from coexisting biotite-garnet pairs, and from the equilibria: paragonite (in white mica) + quartz ± albite (in plagioclase) + Al silicate + H2 O; and, 3 anorthite ± grossular + 2 Alsilicate + quartz. The P-T evolution is correlated with the continuous change in composition of minerals (using P–XMg and T–XMg diagrams) and with the evolution of assemblages. This continuous P-T-time evolution, correlated with the successive formation of S1 -S2 foliations, allows us to propose a P-T-time-deformation path for the micaschists and to relate the growth of its mineral components to tectonic processes. 相似文献
4.
Abstract Andalusite-bearing veins formed during contact metamorphism in the aureole of the Vedrette di Ries tonalite. In the veins, quartz crystals that are completely armoured by andalusite or that occur in strain shadow areas contain three generations of fluid inclusions: low-salinity H2 O-CO2 -CH4 mixtures with CH4 /(CO2 + CH4 ) ± 0.35 (type A); low-salinity aqueous fluids (type B); H2 O-free, CO2 -CH4 fluids with the same carbonic speciation as A (type C). Carbonic types A and C typically have a dark appearance, which is attributed to graphite coatings on inclusion walls. Microstructural analysis of the host quartz and calculated densities indicate that type A inclusions were likely trapped during vein formation. These inclusions underwent strain-assisted re-equilibration during cooling that resulted in density increases without change of composition. After the rocks had cooled below about 350 ° C, type C inclusions appear to have formed from one of the immiscible fractions after unmixing of the H2 O-CO2 -CH4 fluid mixtures. Aqueous type B inclusions, apparently trapped between 225 and 350 ° C, could represent an independent fluid, or could be the H2 O-rich fraction of unmixed type A fluids. Taking account of the uncertainties, the composition and density of the complex type A inclusion fluids are in good agreement with the properties of primary fluids calculated from the petrological data. The fluid inclusion data support the model of vein formation by hydrofracturing as a result of dehydration of graphitic metapelites. These new results also demonstrate the importance of considering strain in the interpretation of metamorphic fluid inclusions. 相似文献
5.
Oxygen Isotopic Characteristics of Granitic Intrusions Related to Haobugao Zn-Pb-Cu-Sn Skarn Deposit, East Inner Mongolia, China 总被引：2，自引：0，他引：2
Jingbin Wang Lijuan Wang Yuwang Wang Tiejun Li Hidehiko Shimazaki 《Resource Geology》2004,54(2):205-208
Abstract. Granitic rocks related to the formation of Haobugao Zn-Pb-Cu-Sn skarn deposit, Inner Mongolia, China, show unusual low whole-rock δ18 O values down to -8.8 % (V-SMOW), whereas separated quartz crystals from those rocks give positive δ18 O values of+4.1 to +9.9 %. Chemical analyses and microscopic observation of those granitic rocks confirm that they suffered hydrothermal alteration. Some skarn specimens and quartz from the Haobugao deposit also show negative δ18 O values. The isotopic evidence indicates that intensive meteoric water circulation occurred at the time of granitic intrusion, and caused the pervasive hydrothermal alteration of granitic rocks and the precipitation of skarn deposit in this area. 相似文献
6.
Bhaskar Chandra ACHARYA Prasanta Kumar PANIGRAHY Binod Bihari NAYAK Rama Krishna SAHOO 《Resource Geology》1998,48(2):125-136
Abstract: Ilmenite, hematite, garnet, monazite, zircon, rutile, magnetite, sillimanite, pyroxene and amphibole from the beach sands of Ekakula, Gahiramatha coast, Orissa, India are reported here for the first time. Their total concentration varies from 26. 4 to 100%. Ilmenite, monazite and zircon are between 100 and 300 um in size and are well rounded in shape. Ilmenite-hematite intergrowth is common. Ilmenite has 50. 02–54. 73% TiO2 , 42. 42–46. 90% FeO (total Fe) and small amounts of Al, Mn, Mg, Ca, Ba, Si, V, Cr, and Zn. The bulk samples contain 10. 63–41. 42 % TiO2 , 6. 15–26. 07 % FeO, 5. 86–16. 75 % Fe2 O3 , 7. 41–61. 74 % SiO2 , 1. 39–12. 83% A12 O3 , 0. 32–4. 97% CaO, 0. 53–4. 24% P2 O5 , 0. 17–3. 27% MgO, 0. 15–2. 97% Na2 O, 0. 07–2. 34% K2 O, and 0. 05–0. 71% V2 O5 together with appreciable amounts of La, Ce, Pr, Nd, Sm, Eu, Y, U, Th, Zr, and trace amounts of Pb, Zn, Cu, Ni, Co, and Cr. Khondalite, charnockite, calc-silicate granulite, leptynite, migmatite, gneiss, basic granulite and pegmatite of the Eastern Ghats appear to be the major source for the above heavy mineral assemblages. The samples are amenable to gravity and magnetic methods of beneficiation. 相似文献
7.
Determinations of the absolute age of cleavage formation can provide fundamental information about the evolution of orogenic belts. However, when applied to cleavages in slates and phyllites, conventional dating methods are complicated by problems related to mineral separation and the presence of multiple cleavage generations. In situ high-spatial-resolution 40 Ar/39 Ar laser microprobe geochronology and microstructural observations indicate that the age of cleavage formation in slates and phyllites can be constrained by analysing zones of tightly packed cleavage domains. Three regionally developed cleavages (S2 , S3 , and S4 ) are present in the northern Taconic Allochthon of Vermont and New York. Representative samples were studied from a variety of localities where these cleavages, which are defined by white micas, are well developed. In the suite of samples, only S3 and S4 are expressed as domains that are sufficiently wide and spatially isolated in thin section to permit quantitative 40 Ar/39 Ar geochronology. Mean 40 Ar/39 Ar laser microprobe ages for these domains are 370.7 ± 1.0 Myr for S3 and 345.5 ± 1.7 Myr for S4 . Because estimates of the Ar closure temperature for white micas are substantially higher than the inferred growth temperatures of the micas defining S3 and S4 , these values are interpreted as periods since cleavage formation. This interpretation is consistent with independent geochronological constraints on the age of the Acadian orogeny in the region. 相似文献
8.
Abstract Clinopyroxenes and garnets from 11 blueschist-facies Fe-rich eclogite samples from the Voltri Group show a wide range of chemical compositions. Detailed analyses of single pyroxene and garnet grains show wide and scattered chemical inhomogeneity, the KD (KD = (Fe2+ /Mg)Gt /(Fe2+ /Mg)Cpx ) ranges from 20 to 87 based on rim analyses only. The data obtained indicate that the mineral pairs never attained equilibrium under uniform P-T conditions and that the compositions of the metamorphic minerals were influenced mainly by the composition of the pre-metamorphic minerals and by topotactical reactions. 相似文献
9.
Viorica Morogan 《地学学报》1994,6(2):166-176
Ijolite-carbonatite complexes are ubiquitously surrounded of an aureole of metasomatically altered rocks. The process of alteration is termed fenitization and is generally caused by peralkaline fluids emanating from cooling alkaline, i.e. ijolite and carbonatite magmas. Ijolites and carbonatites normally occur together and attempts to determine the source of the fenitizing fluids may therefore lead to controversial, if not erroneous, conclusions.
Mineralogical and chemical data of fenites from Oldoinyo Lengai (Tanzania), Fen (Norway), and Alnö (Sweden) are reviewed in the present paper in order to reveal the main factors controlling the fenitization around ijolite and carbonatite. Despite the overall alkaline nature of the process, variables such as XCO2 of the fluid, activity gradients of SiO2 , Al2 O3 and CaO, FeO/MgO ratio, f O2 and temperature gradients may differ, producing distinctive patterns of fenitization around the two magmatic sources. The ijolitic-type fluid has low XCO2 , high activities of alkalies, SiO2 and Al2 O3 , and low activity of CaO. The f O2 evolves along the hm-mt buffer conditions and the temperature falls gradually with distance from the magmatic source. The carbonatitic-type fluid has high XCO2 , high activities of alkalies and CaO, and low activities of SiO2 and Al2 O3 . Temperatures and f O2 are initially high, but decrease sharply with distance from the source. Moreover, the CO2 -rich fluid may complex and transport the REE. 相似文献
Mineralogical and chemical data of fenites from Oldoinyo Lengai (Tanzania), Fen (Norway), and Alnö (Sweden) are reviewed in the present paper in order to reveal the main factors controlling the fenitization around ijolite and carbonatite. Despite the overall alkaline nature of the process, variables such as XCO
10.
Abstract: A strange, unidentified, Cu-Fe bearing zinc sulfide occurs in the Laloki massive sulfide deposit, Papua New Guinea. The mineral is optically uniform in texture but is chemically variable and zoned even within a single grain. Copper contents vary from 0.1 up to 8.85 wt%. Iron reaches 18.31 wt% at maximum and decreases as Cu increases. It is remarkable, however, that the total Fe+Cu remains essentially unchanged between roughly 18 and 20 wt%. Zn and S are least variable, giving 45.85–47.84 wt% and 33.48–34.58 wt%, respectively. Other trace elements such as Cd and Mn are in general less than 0.2 wt%. It is strongly suggested that the mineral in question constitutes a unique Fe-Cu substitutional solid solution series belonging essentially to the Zn–Fe–Cu–S system.
The ideal chemical formula of the solid solution series can well be presented as Zn10 (Fe, Cu)5 S15 or Zn2 (Fe, Cu)S3 , where Fe is always greater than Cu. It is intriguing that chalcopyrite blebs are recognizable restrictively only in nearby portions of the Cu-rich end member with the ideal composition close to Zn10 Fe3 Cu2 S15. It has been confirmed by vacuum-sealed heating experiments that this mineral is decomposed to produce chalcopyrite and Fe-bearing normal sphalerite at temperatures below 200C. This would provide another evidence for the existence of such distinct phase as suggested here. 相似文献
The ideal chemical formula of the solid solution series can well be presented as Zn
11.
Vesna Zajkova Paneva Katarina Cundeva Trajce Stafilov 《Geostandards and Geoanalytical Research》2007,31(1):51-60
A method for the selective separation of Ag, Cd, Cr, Cu, Ni, Pb and Zn in traces from solutions of calcite (CaCO3 ), dolomite (CaMg(CO3 )2 ) and gypsum (CaSO4 .2H2 O) before their determination by inductively coupled plasma-atomic emission spectrometry (ICP-AES) is presented. The expected interferences of Ca and Mg on intensities of trace analytes were removed by collecting the elements of interest with cobalt(III) hexamethylenedithiocar-bamate, Co(HMDTC)3 . The flotation of aqueous solutions (1 l) of calcite, dolomite and gypsum was performed at pH 6.0, by 1.5 mg l−1 Co and 0.6 mmol l−1 HMDTC− . To minimise the effect of the reaction between Ca/Mg, which restrains the function of the surfactant, careful selection of the most suitable foaming reagent was necessary. The accuracy of the method was established by analysing natural alkaline-earth minerals by the standard addition method as well as using the dolomite reference materials GBW 07114 and GSJ JDo-1. The ICP-AES limits of detection following flotation on different minerals were found to be 0.080 μg g−1 for Cd, 0.105 μg g−1 for Ag, 0.142 μg g−1 for Cu, 0.195 μg g−1 for Cr, 0.212 μg g−1 for Ni, 0.235 μg g−1 for Zn and 0.450 μg g−1 for Pb. 相似文献
12.
The chemical analysis by EMPEDS of 140 samples in cores from six Red Sea troughs and basins has led to the discovery in the Nereus Deep of high vanadium concentrations (up to 1.3% V2 O3 ) in several bulk samples, and to the isolation of a major magnetite phase. This vanado-magnetite, remarkable for its high content of vanadium (mean = 1.45% V2 O3 ) and its lack of titanium, is frequently zoned, the V-content decreasing toward the outer zones. Oxides with up to 42% V2 O3 , have also been found. Since the origin of the magnetite is clearly authigenic, its high vanadium and low titanium concentrations are traced back to the differential hydrothermal leaching of Fe—Ti-oxides which occur profusely in basic eruptive rock clasts, actually present in some of the overlying seams. 相似文献
13.
Yoshinobu Aramaki Takushi Yokoyama Yoshihiro Okaue Akira Imai Koichiro Watanabe 《Resource Geology》2005,55(3):281-284
Abstract. Silica scales containing large amounts of smectite were recently found in the pipelines for geothermal water at a geothermal power plant. To elucidate the mechanism of smectite formation, seven silica scale samples were characterized by powder X-ray diffraction, chemical analysis and 27 A1 MAS NMR. Smectite was present in samples with MgO levels above 10 wt% and Al2 O3 levels below 10 wt%. In 27 A1 MAS NMR spectra, peaks assigned to both tetrahedrally and octahedrally coordinated aluminum (Al(4) and Al(6)) were observed for Mg-rich samples, whereas a peak due to Al(4) alone appeared in Mg-poor samples. From these observation and comparison between 27 A1 MAS NMR spectra for synthesized precipitates of Al2 O3 -SiO2 containing MgO and not containing MgO, it is concluded that magnesium plays an important role in the stabilization of Al(6), and results in the formation of smectite 相似文献
14.
Abstract: To determine the geochemical characteristics of the Imgok creek impacted by acid mine drainage (AMD) generated from the abandoned Youngdong coal mine in Korea, chemical analyses of water samples and precipitates and the geochemical modelling of the precipitates were conducted. Acid mine drainage drained from the mine adit and coal refuse piles shows a low pH, high conductivity and high concentrations of Fe, Al, SO4 and heavy metals such as Co, Cu, Ni and Zn. In the Imgok creek, the concentrations of heavy metals and major cations besides Fe are decreased by dilution, but concentrations of Fe are decreased by the formation of precipitates as well as dilution. From the results of geochemical modelling, goethite is oversaturated, and schwertmannite is the most stable solid phase in the Imgok creek. Yellowish red Fe-precipitates collected at the Imgok creek are recognized as amorphous or poorly crystallized minerals from XRD patterns and Feox /Fetot ratios, and as containing chemically bonded SO4 and OH by an IR analysis. The mole ratios of Fe/S in these precipitates, which are determined by EPMA, are 5. 1 and 6. 1. 相似文献
15.
黑龙江省老柞山金矿床位于兴蒙造山带东段佳木斯地块的中北部,是佳木斯金多金属成矿区的一座大型矿床,金主要赋存在NW向、NWW向的张性断裂及花岗岩和钙质大理岩、钙质片麻岩的接触构造带内,成矿与矽卡岩密切伴生。根据野外和室内研究,成矿阶段可划分为矽卡岩阶段、氧化物阶段、早期石英硫化物阶段、晚期石英硫化物阶段和石英-方解石阶段。为揭示流体演化过程,本文选择石榴子石、石英和方解石开展了流体包裹体研究。包裹体岩相学显示,流体包裹体类型有含子晶三相、气液两相（富液相、富气相）、纯液相和纯气相包裹体。测温结果表明：从早到晚均一温度依次为448~462、240~509、166~480、118~360和57~230℃;在矽卡岩阶段盐度（w（NaCl））为9.21%~10.37%,在氧化物阶段为1.73%~13.77%,中低盐度,在早期石英硫化物阶段为1.73%~23.71%和23.64%~39.66%,在晚期石英硫化物阶段为3.05%~6.44%,在石英-方解石阶段为1.73%~11.95%。高温中低盐度且富含CO2、H2O和少量CH4的初始成矿流体,在氧化物阶段流体"沸腾",CO2逃逸,生成磁铁矿;在早期石英硫化物阶段流体持续沸腾,pH值升高,由氧化转化为还原,卸载金和毒砂、黄铁矿等硫化物;在晚期石英硫化物阶段温度降低,卸载方铅矿、闪锌矿等低温矿物和金。因此,推测老柞山金矿床属于矽卡岩型金矿床。 相似文献
16.
Abstract: The Karlapat bauxite deposit occurs in the Eastern Ghat Group of rocks in Orissa and has developed in the khondalites. Mineralogical and physical observations on bore hole samples reflect the presence of a maximum of six weathered zones from top to bottom. These zones are termed as topsoil, siliceous laterite, ferruginous laterite, bauxite, lithomarge and altered khondalite. Four-dimensional trend surface models are developed for the data of 45 and 36 bore holes from north and south blocks, respectively, on Al2 O3 and SiO2 to delineate the zones of metallurgical grade bauxite (SiO2 5 % and Al2 O3 40 %). The results indicate about 15 m thickness of bauxite in the north block while it could be up to 20 m thick in the south block, leaving about 10 m of lat-erites at the top of each block. High grade bauxite (>47 % Al2 O3 ) is also encountered at specific locations. 相似文献
17.
新疆维宝铅锌矿床位于东昆仑祁漫塔格地区西段,铅锌矿体受地层及岩性控制,多呈层状、似层状赋存于蓟县纪狼牙山组中下部条带状绿帘石（透辉石）矽卡岩中,矿石类型主要为绿帘石-透辉石矽卡岩型铅锌（铜）矿石。矿石矿物主要为方铅矿、闪锌矿、黄铜矿等,脉石矿物主要为透辉石、绿帘石、方解石、绿泥石、石榴子石等。金属硫化物电子探针分析表明,闪锌矿中Fe质量分数为2.206%~2.679%,贫Ga、Ge、Cd,Zn/Cd为143~150,方铅矿中Ag质量分数较低（0.163%~0.210%）,具有与岩浆热液有关的金属硫化物特征。流体包裹体以富气相两相包裹体和富液相两相包裹体为主,均一温度平均值分别为268.2和273.1 ℃,含有CO2、CH4、N2、H2等成分,成矿流体可能来源于岩浆流体,具中温、高盐度、低密度的特征,成矿过程中发生了不混溶作用。金属硫化物的δ34SV-CDT为0.49‰~2.41‰,主要来源于岩浆;金属硫化物的206Pb/204Pb为18.254~18.336,207Pb/204Pb为15.556~15.664,208Pb/204Pb为38.060~38.367,主要来源于区内深源岩浆活动,有少量地壳铅的混染。综合分析认为维宝铅锌矿床为与印支期岩浆作用有关的层控矽卡岩型矿床。 相似文献
18.
A sequence of regional metamorphic isograds indicating a range from prehnite-pumpellyite to lower amphibolite facies was mapped in metabasites near Flin Flon, Manitoba. The lowest grade rocks contain prehnite + pumpellyite and are cut by younger brittle faults containing epidote + chlorite + calcite. Isobaric temperature- X CO2 and pressure-temperature (constant X CO2 ) diagrams were calculated to quantify the effects of CO2 in the metamorphic fluid on the stability of prehnite-pumpellyite facies minerals in metabasites containing excess quartz and chlorite. Prehnite and, to a lesser extent, pumpellyite are stable only in fluids with X co2 <0.002. For X co2 >0.002, epidote + chlorite + calcite assemblages are stable. Our calculated phase relations are consistent with regional metamorphism in the Flin Flon area in the presence of an H2 O-rich fluid and a more CO2 -rich fluid in the later fault zones. We believe that the potential effects of small amounts of CO2 in the metamorphic fluid should be assessed when considering the pressure-temperature implications of mineral assemblages in low-grade metabasites. 相似文献
19.
J.LR. Touret 《地学学报》1992,4(1):87-98
The CO2 atmospheric content has shown large variations over geological times. High contents (up to one order of magnitude more than present-day values) ultimately correspond to discrete episodes of mantle degassing, either juvenile, or subduction-related (carbon recycling). A number of arguments (e.g. the continuous volume increase of carbonate-bearing sediments with time) suggest that, throughout the Earth's history, juvenile CO2 has formed a major contribution to the global carbon budget of the Earth.
The absence of a direct relationship between major volcanic episodes and the average CO2 atmospheric content suggests that volcanoes might not be the only way by which mantle CO2 is transported to the surface. It is proposed that large quantities of juvenile CO2 could temporarily be stored in the lower continental crust during major episodes of granulite formation. These are primarily caused by magmatic underplating and they result in a vertical accretion of the crust by accumulation of CO2 -bearing, mantle-derived magmas. Most of the CO2 migrates through the crust during post-metamorphic evolution and isostatic restoration of the normal continental thickness. However, large quantities of CO2 can still be present in some areas, notably as high-density fluids enclosed in minerals. 相似文献
The absence of a direct relationship between major volcanic episodes and the average CO
20.
J. V. WALTHER 《Journal of Metamorphic Geology》1992,10(6):789-797
The equilibrium constant, K a , of the association reaction to form ion pairs from charged solute species in supercritical solutions can be calculated from a model based on published equations. Log K a at constant pressure is a linear function of the inverse in the dielectric constant of the fluid times temperature. The dielectric properties of H2 O and CO2 at supercritical pressures and temperatures can also be evaluated using the Kirkwood equation. Using Looyenga mixing rules, the dielectric constant of H2 O–CO2 mixtures can be obtained and the change in log K a with addition of CO2 in aqueous solutions evaluated. These changes in log K a with addition of CO2 are consistent with measured changes of log K a with addition of Ar in supercritical H2 O–Ar solutions.
Log Ka of KCl and NaCl increase to an increasing extent as the mole fraction of CO2 increases in H2 O–CO2 solutions. For instance, at 2 kbar and constant temperature between 400 and 600° C, log K a of KCl increases by about two orders of magnitude whilst that of NaCl increases by over four orders of magnitude as the CO2 mole fraction increases from 0.0 to 0.35. Such changes in log K a will have dramatic effects on the solubility of minerals in CO2 -rich environments. 相似文献
Log K