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1.
Pegmatite quartz from different occurrences in Norway and Namibia was investigated by a combination of ICP-MS, Electron Spin Resonance (ESR), Capillary Ion Analysis (CIA) and Gas Chromatography (GC) to quantify trace elements in very low concentrations and to determine their position in the quartz structure.The studied quartz samples show similar geochemical characteristics with low contents of most trace elements. Remarkable are the elevated concentrations of Al (36-636 ppm), Ti (1.6-25.2 ppm), Ge (1.0-7.1 ppm), Na (5.2 to >50 ppm), K (1.6 to >100 ppm) and Li (2.1-165.6 ppm). These elements are preferentially incorporated into the quartz lattice on substitutional (Al, Ti, Ge) and interstitial (Li, Na, K) positions. Li+ was found to be the main charge compensating ion for Al, Ge and Ti, whereas some ppm of Na and K may also be hosted by fluid inclusions. Ti may be incorporated as substitutional ion for Si or bound on mineral microinclusions (rutile). The results of the ESR measurements show that there may be a redistribution of alkali ions during irradiation. The diamagnetic [AlO4/M+]0 center transforms into the paramagnetic [AlO4]0 center, whilst the compensating ions diffuse away and may be captured by the diamagnetic precursor centers of [GeO4]0 and [TiO4]0 to form paramagnetic centers ([TiO4/Li+]0, [GeO4/Li+]0).In general, fluid inclusions in pegmatite quartz can be classified as H2O-CO2-NaCl type inclusions with water as the predominant volatile. Among the main elements hosted by fluid inclusions in quartz are Na, K, NH4, Ca, Mg and the anionic complexes Cl−, NO3−, HCO3− and SO42−. Gas analysis of trapped fluids shows volatile components in the following order of abundance: H2O > CO2 > N2(+) ≥ CH4 > COS > C2 and C3 hydrocarbons. Additionally, traces of Co, Ni, Zn, Pb, and Cu were detected by CIA in fluid inclusions of some samples. There are indications that the REE and Rb are also bound in fluid inclusions, however, the concentrations of these elements are too low to be measured by CIA. Assuming that the REE preferentially occur in fluid inclusions, the typical chondrite normalized REE distribution patterns with tetrad effects and a distinct negative Eu anomaly would reflect the composition of the mineralizing fluid.For a number of elements, especially those with extremely low concentrations, the “type” of incorporation in quartz could not directly be determined. We conclude that these ions either are too large to substitute for the small Si4+ ion or they are not soluble in the mineralizing fluids to be hosted by fluid inclusions. Some of these elements, which are concentrated in the specific mineralization of certain pegmatites, are not present in elevated concentrations in the paragenetic pegmatite quartz itself. This was observed, for instance, for Be, Cs and Rb in the Li (Be-Cs-Rb) pegmatites of Rubicon or for Nb and Ta for Nb-Ta bearing pegmatites from Norway. It may be concluded that the concentrations of these trace elements in quartz do not reflect the mineralization and that these elements thus, cannot be used as petrogenetic indicator.  相似文献   

2.
《Applied Geochemistry》2006,21(8):1322-1334
The Ervedosa Mine, in north-eastern Portugal, has Sn-bearing quartz veins containing cassiterite and sulphides that cut Silurian schists and a Sn-bearing muscovite granite. These veins were mined for Sn and As2O3 until 1969. Cassiterite, the main Sn ore, has alternate lighter and darker growth-zones. The darker zones are richer in Fe, Nb, Ta and Ti, but poorer in Sn than the adjoining lighter zones. Exsolution blebs of ferrocolumbite, manganocolumbite, Ti ixiolite, rutile, ilmenite and rare wolframite were found in the darker zones. Arsenopyrite is the most abundant sulphide and contains inclusions of pyrrhotite, bismuth, bismuthinite and matildite. Other sulphides are pyrite, sphalerite, chalcopyrite and stannite. Secondary solid phases consisting mainly of hydrate sulphate complexes of Al, Fe, Ca and Mg (aluminocopiapite, copiapite, halotrichite, pickeringite, gypsum and alunogen, meta-alunogen) occur at the surface of the Sn-bearing quartz veins and their wall rocks (granite and schist), while oxides, hydroxides, arsenates and residual mineral phases (albite, muscovite and quartz) occur in mining tailings. Toxic acid mine waters (acid mine drainage AMD), which have high conductivity and significant concentrations of As, SO4 and metal (Cu, Zn, Pb, Fe, Mn, Cd, Ni and Co), occur in an area directly affected by the mine. Surface stream waters outside this area have low conductivity and a pH that is almost neutral. Metal and As concentrations are also lower. Stream waters within the impact area have an intermediate composition, falling between that of the AMD and the natural stream waters outside impact area. Waters associated directly with mineralised veins must not be used for human consumption or agriculture.  相似文献   

3.
Nanometric solid inclusions in diamond incorporated in garnet and zircon from felsic gneiss of the Kokchetav massif, Kazakhstan, have been examined utilizing electron microscopy and focused ion beam techniques. Host garnet and zircon contain numerous pockets of multiple inclusions, which consist of 1–3 diamond crystals intergrown with quartz, phengite, phlogopite, albite, K‐feldspar, rutile, apatite, titanite, biotite, chlorite and graphite in various combinations. Recalculation of the average chemical composition of the entrapped fluid represented by multiple inclusion pockets indicates that such fluid contained a low wt% of SiO2, suggesting a relatively low‐temperature fluid rather than a melt. Transmission electron microscopy revealed that the diamond contains abundant nanocrystalline inclusions of oxides, rare carbonates and silicates. Within the 15 diamond crystals studied, abundant inclusions were found of SiO2, TiO2, FexOy, Cr2O3, ZrSiO4, and single grains of ThxOy, BaSO4, MgCO3, FeCr2O4 and a stoichiometric Fe‐rich pyroxene. The diversity of trace elements within inclusions of essentially the same stoichiometry suggests that the Kokchetav diamond crystallized from a fluid containing variable amounts of Si, Fe, Ti, Cr, Zr, Ba, Mg and Th and other minor components such as K, Na, P, S, Pb, Zn, Nb, Al, Ca, Cl. Most of the components in crystals included in diamond appear to have their origin in the subducted metasediments, but some of them probably originate from the mantle. It is concluded that Kokchetav diamond most likely crystallized from a COH‐rich multicomponent supercritical fluid at a relatively low temperature (hence the apparently low content of rock‐forming elements), and that the diversity of major and minor components suggests interactions between subducted metasediments and mantle components.  相似文献   

4.
Fluid inclusions in the Merensky Reef quartz and later pegmatite veins crosscutting the Platreef rocks of the Bushveld Complex are studied by a suite of advanced high-precision methods. Based on the conducted studies, we identify a few types of fluids, some having been separated during the crystallization of volatile matter-rich residual melt of original basic magma, while others are derivatives of later felsic (granite) melts that formed crosscutting veins in fully devitrified ultrabasic and basic rocks. The earliest fluid is captured by quartz in symplectitic intergrowths with intercumulus plagioclase from the Merensky Reef pyroxenite occurs as a homogenous dense dry reduced gas (CH4–N2 ± CO2) mixture separated from the aluminosilicate melt at 800–900°C and 3050 bar. The following heterophase highly concentrated fluids (60–80 wt % NaCl eq.) separated at over 550°C and below 3050 bar transport a large number of metals. Major saline components of such fluids included Na, K, Fe, Ca, and Mn chlorides, Ca and Na sulphates and carbonates. According to LA ICP-MS analysis data, inclusions of these fluids contain high concentrations of Fe, Cr, K, and Na at the level of a few wt % and also significant contents of Cu, Sn, Sb, Mo, Au, Ag, Bi, and Ni in a concentration range from a few to thousands of ppm. Relatively lower-temperature (much higher than 450°C) fluids accompanying the crystallization of crosscutting quartz–feldspar pegmatite veins at the Platreef are also highly concentrated (from 70–80% to 40–14 wt % NaCl eq.), oxidized and metal-bearing. High concentrations of metals such as Na, K, Ca, Mn, Fe, and Pb at the level of wt % and also Ni, Co, Cu, As, Mo, Sn, Sb, and Bi (1–500 ppm) in inclusions in quartz of later pegmatite veins suggest the possible participation of magmatogene fluids related to later felsic intrusions in the redistribution of primary magmatic concentrations of metals. The oxidation of reduced heterophase fluids may be the most important geochemical barrier invoking the crystallization of solid mineral phases from heterophase fluids.  相似文献   

5.
《Applied Geochemistry》2000,15(9):1265-1290
Massive sulphide deposits of the northern Iberian Pyrite Belt (IPB) are mainly hosted by felsic volcanic rocks of rhyolitic to dacitic composition. Beneath most of the massive ores of this area (e.g., Concepción, San Miguel, Aguas Teñidas Este or San Telmo deposits) there is usually a wide hydrothermal alteration halo associated with stockwork-type mineralization. Within these alteration envelopes there are two principal rock types: (1) chlorite-rich rocks, linked to the inner and more intensely altered zones and dominantly comprising chlorite+pyrite+quartz+sericite (+carbonate+rutile+zircon+chalcopyrite), and (2) sericite-rich rocks, more common in the peripheral zones and showing a dominant paragenesis of sericite+quartz+pyrite+chlorite (+carbonate+rutile+zircon+sphalerite). Mass-balance calculations comparing altered and least-altered felsic volcanic rocks suggest that sericitization was accompanied by moderate enrichment in Mg, Fe and H2O, with depletion in Si, Na and K, and a slight net mass loss of about 3%. Chloritization shows an overall pattern which is similar to that of the sericitic alteration, but with large gains in Fe, Mg and H2O (and minor enrichment in Si, S and Mn), and a significant loss of Na and K and a minor loss of Ca and Rb. However, chloritization has involved a much larger net mass change (mass gain of about 28%). Only a few elements such as Nb, Y, Zr, Ti, P and LREE appear to have remained inert during hydrothermal alteration, whilst Ti and Al have undergone very minor mobilization. The results point to the severity of the physico-chemical conditions that prevailed during the waxing stage of the ore-forming hydrothermal systems. Further, mineralogical and geochemical studies of the altered footwall rocks in the studied deposits indicate that hydrothermal ore-bearing fluids reacted with host rocks in a multi-stage process which produced a succession of mineralogical and chemical changes as the temperature increased.  相似文献   

6.
作为战略性矿产资源之一,高纯石英已广泛应用于集成电路、半导体芯片、太阳能等高新技术产业中,但是能够生产高纯石英的原料矿床极为稀缺,我国尤为紧缺高纯石英原料矿。鄂东南地区是湖北省脉石英矿床的主要分布区。本文针对鄂东南付家山脉石英矿床,通过光学显微镜、扫描电子显微镜观察了脉石英的脉石矿物类型和包裹体特征,采用电感耦合等离子发射光谱法(ICP-OES)对原矿进行了微量元素分析,旨在获得付家山脉石英矿床的杂质元素特征,进而评价矿床用作高纯石英原料的潜力。结果表明,付家山脉石英矿石SiO2含量大于99.95%,杂质元素主要为Al、K、Fe、Ti、Ca等,脉石矿物主要有白云母、钾长石、铁氧化物等,流体包裹体较为发育。杂质元素分析结果表明,付家山脉石英原矿质量达到低端高纯石英标准,经传统工艺提纯后,可能具有生产中高端高纯石英的潜力。  相似文献   

7.
川西甲基卡二云母花岗岩和伟晶岩内发育大量原生熔体包裹体和富晶体流体包裹体。为了查明甲基卡成矿熔体、流体性质与演化特征,运用激光拉曼光谱和扫描电镜鉴定了甲基卡花岗伟晶岩型锂矿床中二云母花岗岩及伟晶岩脉不同结构带内的原生熔体、流体包裹体的固相物质。分析结果表明,甲基卡二云母花岗岩石英内熔体包裹体的矿物组合为磷灰石+白云母、白云母+钠长石、白云母+石墨;伟晶岩绿柱石内富晶体流体包裹体的矿物组合主要为刚玉、富铝铁硅酸盐+刚玉+锂辉石、锂辉石+石英+锂绿泥石;伟晶岩锂辉石内富晶体流体包裹体的矿物组合主要为磷灰石、锡石、磁铁矿、石英+钠长石+锂绿泥石、萤石、富钙镁硅酸盐+富铁铝硅酸盐+富铁硅酸盐+石英;花岗岩浆熔体与伟晶岩浆熔体(流体)具有一定的差异,成矿熔体、流体成分总体呈现出碱质元素(Na、Si、Al)、挥发分(F、P、CO_2)含量增高及基性元素(Fe、Mg、Ca)降低的特征;包裹体中子矿物与主矿物的化学成分具有一定的差别,揭示出伟晶岩熔体(流体)存在局部岩浆分异作用,具不混溶性及非均匀性。因此认为,伟晶岩熔浆(流体)为岩浆分异与岩浆不混溶共同作用的产物,挥发分含量的增高(F、P、CO_2)使伟晶岩能够与稀有金属组成各类络合物或化合物,这对于稀有金属成矿起到了至关重要的作用。  相似文献   

8.
流体包裹体LA-ICP-MS(激光剥蚀-电感耦合等离子体质谱仪)分析具有高精度、低检测限、多元素同时微区原位检测的特点,因此在精细刻画成矿过程、深入揭示成矿机理方面具有传统方法无可比拟的优势。通过人工合成石英Na Cl-H2O-Rb-Cs和Na Cl-KCl-Ca Cl2-H2O-Rb-Cs流体包裹体,使用NIST610为外标、显微测温Na Cl等效盐度(电价平衡方法)为内标,建立了流体包裹体L A-ICP-MS分析方法。分析结果的相对误差在±16%以内,绝大部分在±10%以内,相对标准偏差(RSD)小于7%。同时结合国际上推荐的石英标样,使用NIST610为外标、无内标法,建立了石英微量元素LA-ICP-MS分析方法。分析结果表明,石英中主要元素Li、Al和Ti的相对误差在±10%以内,相对标准偏差小于5%。利用建立的方法对鲁西早白垩世王家庄Cu-Mo矿开展了应用研究,结果显示该矿富气相包裹体更富Cu,而含子矿物包裹体富Mo,暗示Cu和Mo可能具有不同的搬运机制,Cu更倾向于气相,Mo则倾向于进入液相,结合流体沸腾现象的存在,这可能是导致该矿上铜下钼分带沉淀的重要因素。此外,从早期岩浆成因石英到成矿期热液石英以及成矿期后石英,微量元素具有明显的Ti降低而Al升高的趋势,暗示成矿元素Cu、Mo的沉淀可能同时还受到温度和流体酸碱度变化的控制。  相似文献   

9.
西天山敦德铁矿床磁铁矿原位LA-ICP-MS元素分析及意义   总被引：5，自引：3，他引：2  
敦德铁矿床是天山成矿带内新近发现并勘查的一处大型海相火山岩型铁矿床。该矿床的矿石可划分为浸染状、稠密浸染状、条带状和块状4种主要类型。其中的条带状矿石包括磁铁矿_矽卡岩条带和磁铁矿_方解石条带2种亚类型。块状矿石内出现围岩或矽卡岩角砾时则构成角砾状矿石,其磁铁矿的成因无甚差异。根据野外观察和矿相显微研究,认为磁铁矿形成于早期矽卡岩阶段后的退化蚀变阶段,之后又被更晚的硫化物阶段和绿泥石_碳酸盐阶段的矿物叠加。敦德磁铁矿内主要发生了Al、Mn、Mg和Zn的类质同象置换,此外,也含有Ti、Si、Ca等次要元素以及Na、K、V、Cr、Ni、Co等多种可检测到的微量元素。磁铁矿内元素含量在空间上显示出直观的差异,由深部到浅部,Mn、Zn含量升高,Si、Ca、Na、K、Pb、Ba、Sr、Sb、Cu等含量降低。在Ti O2_Al2O3_Mg O图解、Ti O2_Al2O3_(Mg O+Mn O)图解和Ca+Al+Mn_Ti+V图解上,敦德磁铁矿的分析数据均投影于热液交代(矽卡岩)成因区域。综上认为,该矿床的磁铁矿可能为热液充填交代成因。  相似文献   

10.
Fluid inclusions and F, Cl concentration of hydrous minerals were analysed in the coesite-pyrope quartzite, the interlayered jadeite quartzite and their country-rock gneiss from the Dora-Maira massif using a combination of microthermometry, Raman spectrometry, synchrotron X-ray microfiuorescence and electron microprobe analysis. Three populations of fluid inclusions were recognized texturally and can be related to distinct metamorphic stages. A low-salinity aqueous fluid occurs in the retrogressed country gneiss and as late secondary inclusions in jadeite quartzite and chloritized pyrope. An earlier secondary population is found in matrix quartz of the jadeite- and pyro-pe-quartzites. This population can be related to the early decompression and so to incipient breakdown of garnet into phlogopite-bearing assemblages. The inclusion fluid is highly saline (up to 84 wt% equivalent NaCl) and contains Na, Ca, Fe, Cu and Zn as major cations. In pyrope quartzite, additional K was found in these brines, which locally coexist with CO2-rich inclusions. The oldest fluid inclusions are preserved in kyanite grains included in fresh pyrope and in pyrope itself. In pyrope, all inclusions have decrepitated and contain magnesite, an Mg-phosphate, sheet-silicate(s), a chloride and an opaque phase, with no fluid preser ved. In contrast, the kyanite inclusions in pyrope preserve primary H2O-CO2 low-salinity fluid inclusions, probably owing to the low compressibility of the kyanite inclusions and host garnet. In spite of in-situ re-equilibration, these inclusions can be interpreted as relics of the dehydration fluid that attended pyrope growth. These correlations between textural and chemical fluid inclusion data and metamorphic stages are consistent with the fluid composition calculated from the halogen content of different generations of phlogopite and biotite. The preservation of different fluid compositions, both in time and space, is evidence for local control and possibly origin of the fluids, in agreement with isotopic data. These results, in particular the absence of CO2 in the jadeite quartzite, are best interpreted in terms of a fluid-melt system evolution. With increasing metamorphism, partitioning of H2O, Na, Ca, Fe and heavy metals into melt (jadeite quartzite) and Mg, Na/K, F, CO2 and P(?) into a residual aqueous fluid can account for depletion in Na, Ca and Fe of the pyrope quartzite. During the retrograde path, a H 2 O rose as melt crystallized, generating the two populations of hypersaline and water-rich fluids that were highly reactive to pyrope. The process of fluid-melt interaction envisioned here coupled with models of melt extraction in subduction zones provides an attractive opportunity for the instantaneous ( < 1 Ma) and selective transport of elements between a downgoing slab and the overlying mantle wedge.  相似文献   

11.
A Fe-Ti-Mn-silicate microspherule from the heavy mineral fraction of crushed geological samples from an underground mine (Kellyam gold deposit, Yakutia) was examined by transmission electron microscopy. The 400-μm microspherule has a complex chemical composition and contains the following elements (in order of decreasing content): O, Ti, Si, Mn, Fe, Al, Mg, Ca, and K. The material of the micro-spherule shows a polyphase structure and chemical heterogeneity with separation into amorphous oxide-silicate (SiO2) and crystalline metallic (α-Ti + FeTi) constituents. The spherical shape and the character of internal heterogeneity suggest that the microspherule was formed owing to the rapid solidification of a melt droplet. The nanoscale heterogeneity of the microspherule is a consequence of a two-stage process. (1) Liquid immiscibility in the initial melt droplet before its solidification resulted in the incomplete spatial separation of Si + Al and Ti + Fe + Mn and appearance of SiO2 globules with admixtures of Al, Ca, K, Mg, Ti, Fe, and Mn approximately 100 nm in size. (2) Chemical heterogeneity developed subsequently both within the globules and within the matrix at the stage of melt solidification or after the solidification. The second-stage chemical heterogeneity was manifested in (a) the separation of heavy minor element oxides (Ti, Fe, and Mn) from the light elements Si, Al, K, Ca, and Mg(?) within the globules and (b) the separation of the matrix material into crystalline metallic (α-Ti + FeTi) and amorphous oxide-silicate [SiO2-MgO-Mn3O4(?)-Fe2O3(?)-TiO2(?)] parts. The obtained results do not rule out the possibility of formation of such microspherules during drilling operations.  相似文献   

12.
Four overbank profiles from the three terraces of different age were sampled in 10 to 20 cm intervals for the bulk content of major and minor (Ca, Mg, Fe, Ti, Al, Na, K and P) and trace (Mo, Cu, Pb, Zn, Ni, Co, Mn, As, U, Th, Sr, Cd, Sb, V, La, Cr, Ba, W, Zr, Ce, Sn, Y, Nb, Ta, Sc, Li, Rb and Hf) elements in the minus 0.125 mm fraction. Univariate statistics together with analysis of variance discriminated between the lower-lying carbonate (CA) population dominantly composed of carbonates and the overlying silicate (SI) population being dominantly of silicate mineralogy. This stratified pattern resulted from the intensive erosive action of melting glaciers exerted on limestones and dolomites in the alpine region, followed by local inputs mainly of silicate composition. Elements exhibiting the greatest between-population variability are Ca and Mg being enriched in the CA population and Fe, Mn, P, Sr, Al, Na, K, Li, Rb, Y, Zr, Ni, Cr and Ti being enriched in the SI population. Anomalously high Hg, Pb and Ba concentrations (maximum values: 6,500±2,860 ppb, 225±13 ppm and 1,519±91 ppm, respectively) in the lowermost part of the profile S7, which is nearest to the Croatian-Slovenian border, derive from the mineralized Slovenian catchment area. This profile also contains trimodal frequency distributions of Fe, Mn and P whose highest concentrations coincide with increased values of Zn and Cu which are bimodally distributed. Geochemical patterns of majority of elements in all four profiles consistently reflect the average compositions of the upstream drainage basins.  相似文献   

13.
Melt inclusions were examined in phenocrysts in basalt, andesite, dacite, and rhyodacite from the Karymskii volcanic center in Kamchatka and dacite form Golovnina volcano in Kunashir Island, Kuriles. The inclusions were examined by homogenization and by analyzing glasses in more than 80 inclusions on an electron microscope and ion microprobe. The SiO2 concentrations in the melt inclusions in plagioclase phenocrysts from basalts from the Karymskii volcanic center vary from 47.4 to 57.1 wt %, these values for inclusions in plagioclase phenocrysts from andesites are 55.7–67.1 wt %, in plagioclase phenocrysts from the dacites and rhyodacites are 65.9–73.1 wt %, and those in quartz in the rhyodacites are 72.2–75.7 wt %. The SiO2 concentrations in melt inclusions in quartz from dacites from Golovnina volcano range from 70.2 to 77.0 wt %. The basaltic melts are characterized by usual concentrations of major components (wt %): TiO2 = 0.7–1.3, FeO = 6.8–11.4, MgO = 2.3–6.1, CaO = 6.7–10.8, and K2O = 0.4–1.7; but these rocks are notably enriched in Na2O (2.9–7.4 wt % at an average of 5.1 wt %, with the highest Na2O concentration detected in the most basic melts: SiO2 = 47.4–52.0 wt %. The concentrations of volatiles in the basic melts are 1.6 wt % for H2O, 0.14 wt % for S, 0.09 wt % for Cl, and 50 ppm for F. The andesite melts are characterized by high concentrations (wt %) of FeO (6.5 on average), CaO (5.2), and Cl (0.26) at usual concentrations of Na2O (4.5), K2O (2.1), and S (0.07). High water concentrations were determined in the dacite and rhyodacite melts: from 0.9 to 7.3 wt % (average of 15 analyses equals 4.5 wt %). The Cl concentration in these melts is 0.15 wt %, and those of F and S are 0.06 and 0.01 wt %, respectively. Melt inclusions in quartz from the dacites of Golovnina volcano are also rich in water: they contain from 5.0 to 6.7 wt % (average 5.6 wt %). The comparison of melt compositions from the Karymskii volcanic center and previously studied melts from Bezymyannyi and Shiveluch volcanoes revealed their significant differences. The former are more basic, are enriched in Ti, Fe, Mg, Ca, Na, and P but significantly depleted in K. The melts of the Karymskii volcanic center are most probably less differentiated than the melts of Bezymyannyi and Shiveluch volcanoes. The concentrations of water and 20 trace elements were measured in the glasses of 22 melt inclusions in plagioclase and quartz from our samples. Unusually high values were obtained for Li concentrations (along with high Na concentrations) in the basaltic melts from the Karymskii volcanic center: from 118 to 1750 ppm, whereas the dacite and rhyolite melts contain 25 ppm Li on average. The rhyolite melts of Golovnina volcano are much poorer in Li: 1.4 ppm on average. The melts of the Karymskii volcanic center are characterized by relative minima at Nb and Ti and maxima at B and K, as is typical of arc magmas.  相似文献   

14.
利用电子显微镜(EM)及能谱仪(EDS),分析研究了变生热液形成的载金石英的化学成分、离子扩散作用以及金在石英中的赋存状态等问题,探讨了它们的形成和变化机理。研究结果表明:Al~(3+)、Ti~(3+)、TFe、Na~(+)、K~(+)、Ca~(2+)等在石英中为类质同像混入物;石英和黄铁矿之间的离子相互扩散作用,表现为石英中Al离子的带出和Fe离子的带入,黄铁矿中Fe离子的带出和Al离子的带入;石英中呈分散状态分布的金主要为离子金,它们充填在石英结构中,起平衡电价的作用。  相似文献   

15.
Mechanisms of the incorporation of isomorphic impurities of Al, Ti, and Ge into quartz were studied by EPR techniques. For this purpose, laboratory experiments were carried out on quartz annealing, which allowed us to model the processes of impurity atom introduction into the quartz lattice. The investigation of the kinetics of these processes showed that they are described by diffusion-controlled reactions. In many samples, a proportional relationship was observed between the concentrations of Al and Ti impurities incorporated into the quartz structure during laboratory annealing. A comparison of the experimental results with the character of the natural distribution of isomorphic impurities in quartz revealed their similarity. Based on the analysis of the results of our investigations, two main mechanisms were proposed for isomorphic substitutions in quartz. One of them is referred to as the capture mechanism and corresponds to the incorporation of isomorphic impurities during mineral formation. The second, diffusion mechanism operates after the crystallization of quartz. The isomorphic impurities incorporated into the quartz structure by this mechanism are either formed through the decomposition and transformation of composite complexes or as a result of diffusion from crystalline and gas-liquid inclusions. It was suggested that both mechanisms are responsible for the incorporation of Al and Ge impurities into the mineral lattice, whereas Ti is introduced mainly by the diffusion mechanism. The accounting for the mechanisms of isomorphic substitutions provides a means to significantly increase the reliability of the interpretation of genetic information recorded in the distribution of structural impurities in quartz. Original Russian Text ? L.T. Rakov, 2006, published in Geokhimiya, 2006, No. 10, pp. 1085–1096.  相似文献   

16.
The Soufrière Hills volcano on Montserrat has for the past 12 years been erupting andesite with basaltic to basaltic–andesite inclusions. The andesite contains a wide variety of phenocryst textures and strongly zoned microlites. Analysis of minor elements in both phenocrysts and microlites allows us to put detailed constraints on their origins. Compositions of clinopyroxene, from overgrowth rims on quartz and orthopyroxene and coarse-grained breakdown rims on hornblende, are identical to those from the mafic inclusions, indicating that these rims form during interaction with mafic magma. In contrast, resorbed quartz and reversely zoned orthopyroxenes form during heating. Microlites of plagioclase and orthopyroxene are chemically distinct from the phenocrysts, being enriched in Fe and Mg, and Al and Ca respectively. However, microlites of plagioclase, orthopyroxene and clinopyroxene are indistinguishable from the compositions of these phases in the mafic inclusions. We infer that the inclusions disaggregated under conditions of high shear stress during ascent in the conduit, transferring mafic material into the andesite groundmass. The mafic component of the system is therefore greater than previously thought. The presence of mafic-derived microlites in the andesite groundmass also means that care must be taken when using this as a starting material for phase equilibrium experiments.  相似文献   

17.
Trace elements (Al, K, Ti, Fe), growth and deformation pattern in quartz of the multiple deformed Carcoar, Barry and Sunset Hills granites were investigated by electron micro probe and cathodoluminescence. Zoned quartz phenocrysts with high Ti concentrations (>70 ppm) that show blue cathodoluminescence originated from the early stage of magma crystallisation. Multiple deformation of quartz causes the redistribution of Al and K in the quartz lattice, which results in the accumulation of these elements in submicroscopic inclusions (<0.5 µm) of muscovite-like composition. In contrast, structural Ti in quartz is mostly kept in the lattice. Common halos of defect-poor, secondary quartz around fluid inclusions result from re-equilibration of fluid inclusions because of differences between fluid pressure and lithostatic pressure, e.g. during uplift (isothermal decompression) and/or !/#-transition of quartz. During healing, defect-poor secondary quartz grows at the cost of the host quartz and releases or replaces defect centres. The results of micro-structural investigations combined with Al-in-hornblende thermobarometry allow the reconstruction of regional processes. Carcoar and Barry granodiorites and Sunset Hills granite were intruded in the Late Ordovician-Early Silurian at depths of 4-8.6 and 10-12 km, respectively. In contrast to the continuous crystallisation of the granodiorite magmas, the magma of the Sunset Hills granite ascended in a stepwise fashion, causing multiple quartz nucleation. The two granodiorites were multiple, post-magmatically deformed, first, during Early Devonian under more brittle conditions at temperatures of 350-400 °C, whereas the Sunset Hills granite experienced more ductile deformation at temperatures of around 550 °C.  相似文献   

18.
We analyzed 85 fluid inclusions from seven samples from the porphyry Cu–Mo deposit in Butte, MT, using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). The Butte deposit formed at unusually great depth relative to most porphyry deposits, and fluid inclusions in deep veins trapped a low-salinity, CO2-bearing, magmatically derived, supercritical fluid as a single aqueous phase. This fluid is interpreted to be the parent fluid that cooled, decompressed, unmixed, and reacted with wall rock to form the gigantic porphyry Cu deposit at Butte. Few previous analyses of such fluids exist.Low-salinity, aqueous fluids from the earliest veins at Butte are trapped in deep veins with biotite-rich alteration envelopes (EDM veins). These veins, and the Butte quartz monzonite surrounding them, host much of the Butte porphyry Cu mineralization. Twenty fluid inclusions in one EDM quartz vein are dominated by Na, K, Fe (from 0.1 to 1 wt.%) and contain up to 1.3 wt.% Cu. These inclusions contain only small amounts (tens of ppm) of Pb, Zn, and Mn, and typically contain Li, B, Ca, As, Mo, Ag, Sn, Sb, Ba, and W in less than detectable quantities. The abundance of Cu in early fluids indicates that a low-salinity, Cu-rich, aqueous ore fluid can be directly produced by aqueous fluid separation from a granitic magma. Similar inclusions (eight) in an early deep quartz–molybdenite vein with a K-feldspar selvage have similar compositions but contain significantly less Cu than most inclusions in the biotite-altered vein. Analyzed inclusions in both veins contain less than detectable concentrations of Mo even though one is molybdenite-bearing.Low-salinity, CO2-bearing aqueous fluids are also trapped in pyrite–quartz veins with sericitic selvages. These veins cut both of the above vein types and contain inclusions that were trapped at lower pressure and temperature. Thirty-nine inclusions in two such veins have compositions similar to early fluids, but are enriched by up to a factor of 10 in Mn, Pb, and Zn relative to early fluids, and are slightly depleted in Fe. Many of these inclusions contain as much or more Cu than early fluids, although little chalcopyrite is found in or around pyrite–quartz veins.Eighteen halite-bearing inclusions from three veins from both chalcopyrite-bearing and barren veins with both K-silicate and sericitic selvages were analyzed as well. Halite-saturated inclusions are dominated by Na, K, Fe, and in some inclusions Ca. Whereas these inclusions are significantly enriched in Ca, Mn, Fe, Zn, and Pb, fluids in all three veins contain significantly less Cu than early, high temperature, low-salinity inclusions.Analyses of all inclusion types show that whereas bulk-salinity of the hydrothermal fluid must be largely controlled by the magma, fluid–rock interactions have a significant role in controlling fluid compositions and metal ratios. Cu concentrations range over an order of magnitude, more than any other element, in all four samples containing low-salinity inclusions. We infer that variations are the result of fluid trapping after different amounts of fluid–rock reaction and chalcopyrite precipitation. Enrichment, relative to early fluids, of Mn, Pb, and Zn in fluids related to sericitic alteration is also likely the result of fluid–rock reaction, whereby these elements are released from biotite and feldspars as they alter to sericite. In halite-bearing inclusions, concentrations of Sr, Ca, Pb, and Ba are elevated in inclusions from the pyrite–quartz vein with sericitic alteration relative to halite-bearing inclusions from unaltered and potassically altered samples. Such enrichment is likely caused by the breakdown of plagioclase and K-feldspar in the alteration envelope, releasing Sr, Ca, Pb, and Ba.  相似文献   

19.
We report petrological, cathodoluminescence (CL), major and trace element analyses and fluid inclusion studies on scheelite (W)-mineralized granodiorite porphyries from Dongyuan and Zhuxiling, southern Anhui Province (China). In Dongyuan, the larger part of the granodiorite porphyry body is mineralized with W concentrations up to 1140 g/t (total WO3 reserves >140 000 tonnes), whereas in Zhuxiling mineralization is spatially more limited. All mineralized rocks are strongly altered, containing abundant calcite and no fresh plagioclase. W-mineralized rocks show higher K, Pb and lower Na, Sr, Ti contents compared to the non-mineralized ones. Co-variations between mobile elements (K, Na, Pb, Sr, Rb, etc.) and W, combined with petrological observations, demonstrate that fluid alteration must have controlled the mineralization. In quartz from both deposits 4 types of fluid inclusions have been recognized, i.e., aqueous-carbonic (WC-type), aqueous (W-type, subdivided into Wm-type containing minor detected CO2 and Wn containing no CO2), carbonic (pure CO2, C-type) and late secondary aqueous inclusions (LW-type). WC- and LW-type inclusions represent the original magmatic fluids and meteoric waters, respectively. The other inclusions represent evolved magmatic fluids which are closely related to alteration and mineralization. WC-, Wm- and Wn-type inclusions show higher salinity and lower homogenization temperatures, indicating fluid immiscibility with CO2 effervescence. Additionally, during plagioclase alteration and precipitation of K-feldspar and sericite the K/Na ratio is lowered and Ca released. The precipitation of scheelite must have been promoted by increasing Ca contents in the fluid and also by increasing pH due to CO2 loss. The present study demonstrates that for granitic rocks without calcareous wall rock, plagioclase breakdown must have been the key factor for scheelite mineralization. The presence of CO2-rich fluid indicates that both deposits formed in the same intracontinental extension setting as those in the Nanling region. Thus, the Yanshanian granites from southern Anhui Province may have a great potential for W mineralization, especially the blind ones in deep levels.  相似文献   

20.
Numerous pegmatite dikes occur in the Sparrow pluton (muscovite-biotite granite) and in the adjacent cordierite-zone schist-hornfels of the Yellowknife Supergroup. Where pegmatite dikes cut granite, the adjacent granite is enriched in muscovite and apatite, and depleted in K-feldspar. Mass transfer calculations, based on rock, mineral, and modal analyses, indicate that H, P, and locally B, Ti, Fe, and Ca were added, and K, Sr, Ba, and locally Na were removed (hydrogen metasomatism). In one alteration zone (8 cm wide) the calculated change (in terms of mols/gram of unaltered granite) is, 600 K-feldspar+24 biotite+190 plagioclase +[770 H+36 P+3 Ti+13 Fe+13 Ca] 400 muscovite+1100 quartz +11 apatite+[240 Na+260 K]. Where pegmatite dikes cut schist-hornfels (biotite-plagioclase-quartz), the adjacent rock is, in places, enriched in tourmaline, apatite, and quartz, and depleted in biotite and plagioclase. These alteration zones are variable in width; most are less than 20 cm wide. Mass transfer calculations, based on rock, mineral, and modal analyses, indicate that B, P, Zn, and locally Ca, Fe, and Al were added, and that Na, K, Fe, Rb, Sr, Ba, and locally Mg and Si were removed (boron metasomatism). In one zone, 2 cm wide, the calculated reaction (in units of mols/gram of unaltered schist) is, 730 biotite+1530 plagioclase +[1080 B+600 H+430 P+360 Ca] 480 tourmaline+480 quartz+115 apatite +[3630 Si+870 Na+590 K+110 Fe]. Changes in the volume fraction of muscovite, K-feldspar, tourmaline, and biotite, relative to distance from pegmatite, are progressive, and in most alteration zones may be expressed by use of an error-function equation. Some tourmaline zones are more complex. Zone formation is considered in terms of a steady-state reaction model in which grainboundary diffusion is the transport mechanism.  相似文献   

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