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1.
Exsolution lamellae of pyroxene in garnet (grt), coesite in titanite and omphacite from UHPM terranes are widely accepted as products of decompression. However, interpretation of oriented lamellae of phyllosilicates, framework silicates and oxides as a product of decompression of pyroxene is very often under debate. Results are presented here of FIB‐TEM, FEG‐EMP and synchrotron‐assisted infrared (IR) spectroscopy studies of phlogopite (Phlog) and phlogopite + quartz (Qtz) lamellae in diamond‐bearing clinopyroxene (Cpx) from ultra‐high pressure (UHP) marble. These techniques allowed collection of three‐dimensional information from the grain boundaries of both the single (phlogopite), two‐phase lamellae (phlogopite + quartz), and fluid inclusions inside of diamond included in K‐rich Cpx and understanding their relationships and mechanisms of formation. The Cpx grains contain in their cores lamellae‐I, which are represented by topotactically oriented extremely thin lamellae of phlogopite (that generally are two units cell wide but locally can be seen to be somewhat broader) and microdiamond. The core composition is: (Ca0.94K0.04Na0.02) (Al0.06Fe0.08Mg0.88) (Si1.98Al0.02)O6.00. Fluid inclusions rich in K and Si are recognized in the core of the Cpx, having no visible connections to the lamellae‐I. Lamellar‐II inclusions consist of micron‐size single laths of phlogopite and lens‐like quartz or slightly elongated phlogopite + quartz intergrowths; all are situated in the rim zone of the Cpx. The composition of the rim is (Ca0.95Fe0.03Na0.02) (Al0.05Fe0.05Mg0.90)Si2O6, and the rim contains more Ca, Mg then the core, with no K there. Such chemical tests support our microstructural observations and conclusion that the phlogopite lamellae‐I are exsolved from the K‐rich Cpx‐precursor during decompression. It is assumed that Cpx‐precursor was also enriched in H2O, because diamond included in the core of this Cpx contains fluid inclusions. The synchrotron IR spectra of such diamond record the presence of OH? stretching and H2O bending motion regions. Lamellar‐II inclusions are interpreted as forming partly because of modification of the lamellae‐I in the presence of fluid enriched in K, Fe and Si during deformation of the host diopside; the latter is probably related to the shallower stage of exhumation of the UHP marble. This study emphasizes that in each case to understand the mechanism of lamellar inclusion formation more detailed studies are needed combining both compositional, structural and three‐dimensional textural features of lamellar inclusions and their host.  相似文献   

2.
The Jiangzhuang ultrahigh‐pressure (UHP) metamorphic peridotite from south Sulu, eastern China occurs as a layer within gneiss with eclogite blocks, and consists of coarse‐grained garnet porphyroblasts and a fine‐grained matrix assemblage of garnet + forsterite + enstatite + diopside ± phlogopite ± Ti‐clinohumite ± magnesite. Both types of garnet are characterized by high MgO content and depletion of light rare earth element (LREE) and enrichment of heavy rare earth element, but the matrix garnet has lower MgO, TiO2 and higher Cr2O3 and REE contents. Diopside displays LREE enrichment, and has low but variable large‐ion lithophile element (LILE) contents. Phlogopite is a major carrier of LILE. Ti‐clinohumite contains high Nb, Ta, Cr, Ni, V and Co contents. The P–T conditions of 4.5–6.0 GPa and 850–950 °C were estimated for matrix mineral assemblages. Most peridotites are depleted in Al2O3, CaO and TiO2, and enriched in SiO2, K2O, REE and LILE. In contrast to phlogopite‐free peridotites, the phlogopite‐bearing peridotites have higher K2O, Zr, REE and LILE contents. Zircon occurs only in the phlogopite‐bearing peridotites, shows no zoning, with low REE contents and Th/U ratios, and yields tight U–Pb ages of 225–220 Ma, indicating the peridotites experienced consistent Triassic UHP metamorphism with subducted supercrustal rocks. These data demonstrate that the Jiangzhuang peridotites were derived from the depleted mantle wedge of the North China Craton, and experienced various degrees of metasomatism. The phlogopite‐free peridotites may have been subjected to an early cryptic metasomatism at UHP conditions of the mantle wedge, whereas the phlogopite‐bearing peridotites were subjected to a subsequent strong metasomatism, characterized by distinctly enrichment in LILE, LREE, Zr and K as well as the growth of zircon and volatile‐bearing minerals at UHP subduction conditions. The related metasomatism may have resulted from the filtration of fluids sourced mainly from deeply subducted supracrustal rocks.  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.
An unusually iron-rich, strongly peralkaline dyke occurring near the Ilimaussaq intrusion, south Greenland, is described. The dyke has developed two facies characterised respectively by the mafic assemblages pyroxene+amphibole+aemigmatite, and pyroxene+magnetite. The differences can be explained as an effect of loss of up to 4% Na1O from the magnetite-bearing facies (relative to the magnetite-free facies). The effect is in accordance with the phase relations at 1 atm in the synthetic system Na2OAl2O2Fe2O2SiO2. Continued alkali loss and magnetic precipitation will change the differentiation trend from agpaitic with iron enrichment towards miaskitic with iron depletion. It is suggested that the extreme degree of iron enrichment in the dyke resulted from the coincidence of low oxygen fugacity and strong peralkalinity tending to stabilise both ferrous and ferric iron in the liquid.  相似文献   

5.
The K‐rich granitoids of the southern Mt Angelay igneous complex belong to the younger phases of the Williams and Naraku Batholiths (<1540 Ma) in the Cloncurry district. Granitoids of the complex form a series of I‐type, K‐rich, metaluminous monzodiorite to subaluminous syenogranite. These intrusions have geochemical affinities akin to ‘A‐type’ granites and contain plagioclase, alkali feldspar, quartz, biotite, hornblende and typically accessory magnetite, titanite, apatite and zircon. With increasing SiO2 the granitoids vary from alkaline to subalkaline, and exhibit a decrease in TiO2, Al2O3, Fe2O3*, MnO, MgO, CaO, P2O5, Cu, Sr, Zr, LREE and Eu, with an increase in Na2O, K2O, Rb, Pb, Th, U, Y and HREE. This suite of relatively oxidised granitoids (<1.0 log units above NNO) were emplaced after the peak of metamorphism and pre‐ to post‐D3, a major east‐west horizontal‐shortening event. The synchronous emplacement of high‐temperature mafic (>960°C) and foliated felsic (>900°C) granitoids formed zones of mingled and mixed monzonite and quartz monzonite to monzogranite containing abundant rapakivi K‐feldspar. These intrusions are interpreted to have been derived from source rocks of different compositions, and probably by different degrees of partial melting. The unfoliated felsic granitoids are considered to represent the fractionated equivalents of older foliated felsic granitoids. All granitoids possess a Sr‐depleted and Y‐undepleted signature, which suggests that the source material probably contained plagioclase and no garnet, restricting magma production to <800–1000 MPa (～24–30 km). Underplating of mantle‐derived mafic material into mid‐crustal levels is considered the most viable mechanism to produce these high‐temperature K‐rich granitoids at these pressures. The composition of the felsic granitoids is consistent with derivation from a crustal source with a tonalitic to granodioritic composition. However, the mafic granitoids require a more mafic, possibly gabbroic source, which may have been supplemented with minor mantle‐derived material. These granitoids are also enriched in Th, U, LREE and depleted in Ba, Ti, Nb and Sr and compare closely to the Mesoproterozoic granitoids of the Gawler Craton. The economic significance of these styles of granitoids may also be highlighted by the close spatial relationship of hematitic K‐feldspar, magnetite, fluorite and pyrite‐rich veins, alteration and filled miarolitic cavities with the least‐evolved felsic intrusions. This style of veining has a probable magmatic origin and is similar to the gangue assemblage associated with Ernest Henry‐style Fe‐oxide‐(Cu–Au) mineralisation, which suggests that these granitoids represent prospective sources of fluids associated with Cu–Au mineralisation in the district.  相似文献   

6.
Phlogopite-amphibole-pyroxenite xenoliths contained in the alkali basic-ultrabasic subvolcanic complex in Langao, Shaanxi Province, are composed of diopside, Ti-rich pargasite, phlogopite apatite, sphene and ilmenite, which have subsolidus metamorphism-deformation textures such as triple-points, cataclastic boundaries and kink-bands. Mineral chemical characteristics show that the diposide, Ti-rich paragasite and phlogopite are derived from the mantle and are the products of mantle metasomatism. Compared with normal mantle-derived spinel-lherzolites, the xenoliths are enriched in TiO2, Fe2O3, CaO, Na2O and K2O, with apparent depletion in MgO. Chondrite-normalized REE patterns and primordial-mantle normalized trace elements data show that they are enriched in REE (especially LREE) and incompatible trace elements. The petrographic, mineralogical and petrochemical characteristics indicate that the xenoliths are metasomatized mantle xenoliths, which offers the evidence for mantle metasomatism and represents the anomalous mantle beneath the Early Paleozoic rift in northern Daba Mountains. The agents of mantle metasomatism are probably derived from the rising of mantle hot plumes. The processes of metasomatism varied from limited-range fluid metasomatism in deep mantle (>90 km) to pervasive metasomatism of silicate melt. This project was financially supported by the National Natural Science Foundation of China (No. 49402035).  相似文献   

7.
Lightly altered Al-rich inclusions in amoeboid olivine aggregates have cores containing primary melilite + fassaite + spinel + perovskite and no secondary alteration products. In moderately altered inclusions, whose cores now contain only fassaite + spinel + perovskite, melilite was replaced by a fine-grained mixture of grossular + anorthite + feldspathoids and perovskite was partially replaced by ilmenite. In heavily altered inclusions, fassaite has been replaced by a mixture of phyllosilicates + ilmenite and the remaining primary phases are spinel ± perovskite. In very heavily altered inclusions, no primary phases remain, the spinel having reacted to form either phyllosilicates or a mixture of olivine + feldspathoids. This sequence of alteration reactions may reflect successively lower solar nebular equilibration temperatures. During alteration, SiO2, Na2O, K2O, FeO, Cr2O3, H2O and Cl were introduced into the inclusions and CaO was lost. MgO may have been lost during the melilite reaction and added during formation of phyllosilicates. Electron microprobe analyses indicate that the phyllosilicates are a mixture of Na-rich phlogopite and chlorite or Alrich serpentine. Thermodynamic calculations suggest that, at a solar nebular water fugacity of 10−6, Na-rich phlogopite could have formed from fassaite at ~470 K and chlorite from Na-rich phlogopite at ~328 K. Olivine mantling Al-rich inclusions is not serpentinized, suggesting that these objects stopped equilibrating with the nebular gas above 274 K.  相似文献   

8.
Geochemical characteristics of the Chagande’ersi molybdenum deposit in Inner Mongolia and its genesis were analyzed in this study using rock mineralography and rock geochemical testing. The mineralized country rocks of the Chagande’ersi molybdenum deposit consist mainly of medium-to fine-grained monzogranite,medium-to fine-grained rich-K granite,with minor fine-grained K-feldspar granite veins and quartz veins.The rocks are characterized by high silica,rich alkali,high potassium,which are favorable factors for molybdenum mineralization.The rocks have the Rittmann index ranging from 1.329 to 1.961,an average Na2O+K2O value of 7.41,and Al2O3/（CaO+Na2O+K2O）>1,suggesting that the rocks belong to the high-K calc-alkaline peraluminous granite.The typical rock samples are enriched in Rb,Th,K and light rare earth elements,depleted in Sr,Ba,Nb,P and Ti, and these features are similar to that of the melt granite resulting from collision of plate margins.TheδEu of the rocks falls the zone between the crust granite and crust-mantle granite,and are close to that of the crust granite;（La/Lu）N indicates the formation environment of granite is a continental margin setting.The Nb/Ta ratios are close to that of the average crust（10）;the Zr/Hf ratios of monzogranite are partly below the mean mantle（34-60）,while the Zr/Hf ratio of K-feldspar granite are close to the mean value in the crust.Comprehensive analyses show that the granite in this area formed during the transition period between tectonic collision and post-collision.During the plate collision and orogeny,the crust and mantle material were mixed physically,remelting into lava and then crystal fractionation,finally gave rise to the formation of the rock body in this area.This has close spatial and temporal relation with the molybdenum mineralization.  相似文献   

9.
Systematic analysis and comparative study of the chemical compositons of rocks and ores from the main types of zeolite deposits in the surroundings of the Songliao Basic have shown that the process of formation of zeolite from volcanic and pyroclastic rocks is generally characterized by the relative purification of SiO2,i.e.,SiO2/Al2O3 ratios tend to increase,alkali eart elements (CaO MgO)and H2O are relatively enriched,and the alkali metals(K2O Na2O)are depleted in their total amount.The alkali metals K and Na follow different rules of migration and enrichment during the formation of mordenite and clinoptilolite.In the process of formation of mordenite more Na^ will be imported and K^ will be lost remarkably.On the contrary,in the process of formation clinoptilolite more K^ will be incorporated and Na^ will become obviously depleted.  相似文献   

10.
We experimentally investigated the phase relations of a peralkaline phonolitic dyke rock associated with the Ilímaussaq plutonic complex (South Greenland). The extremely evolved and iron-rich composition (magnesium number = 2, alkalinity index = 1.44, FeO* = 12 wt%) may represent the parental magma of the Ilímaussaq complex. This dyke rock is therefore perfectly suited for performing phase-equilibrium experiments, since in contrast to the plutonic rocks of the complex, no major cumulate formation processes complicate defining a reasonable starting composition. Experiments were carried out in hydrothermal rapid-quench cold-seal pressure vessels at P = 100 MPa and T = 950–750 °C. H2O contents ranging from anhydrous to H2O saturated (~5 wt% H2O) and varying fO2 (~ΔlogFMQ ?3 to +1; where FMQ represents the fayalite–magnetite–quartz oxygen buffer) were applied. Reduced and dry conditions lead to substantial crystallization of alkali feldspar, nepheline, hedenbergite-rich clinopyroxene, fayalite-rich olivine and minor amounts of ulvøspinel-rich magnetite, which represent the phenocryst assemblage of the natural dyke rock. Oxidized and H2O-rich conditions, however, suppress the crystallization of olivine in favor of magnetite and clinopyroxene with less or no alkali feldspar and nepheline formation. Accordingly, combined low fO2 and aH2O force the evolution of the residual melt toward decreasing SiO2, increasing FeO* and alkalinity index (up to 3.55). On the contrary, high fO2 and aH2O produce residual melts with relatively low FeO*, high SiO2 and a relatively constant alkalinity index. We show that variations of aH2O and fO2 lead to contrasting trends regarding the liquid lines of descent of iron-rich silica-undersaturated peralkaline compositions. Moreover, the increase in FeO* and alkalinity index (reduced and dry conditions) in the residual melt is an important prerequisite to stabilize late-magmatic minerals of the dyke rock, for example, aenigmatite (Na2Fe5TiSi6O20), coexisting with the most evolved melts at 750 °C. Contrary to what might be expected, experiments with high aH2O and interlinked high fO2 exhibit higher liquidus T’s compared with experiments performed at low aH2O and fO2 for experiments where magnetite is liquidus phase. This is because ulvøspinel-poor magnetite crystallizes at higher fO2 and has a higher melting point than ulvøspinel-rich magnetite, which is favored at lower fO2.  相似文献   

11.
An absarokite from a phlogopite lherzolite source   总被引：1，自引：0，他引：1  
An absarokite (SiO2 47.72 wt %, K2O 3.41 wt %) occurs in the Katamata volcano, SW Japan. The rock carries phenocrysts of olivine, phlogopite, clinopyroxene, and hornblende. Chemical compositions of bulk rock (FeO*/ MgO 0.73) and minerals (Mg-rich olivine and phlogopite, Cr-rich chromite) suggest that the absarokite is not differentiated. Melting experiments at high pressures on the Katamata absarokite have been conducted. The completely anhydrous absarokite melt coexists with olivine, orthopyroxene, and clinopyroxene at 1310° C and 1.0 GPa. The melt with 3.29 wt % of H2O also coexists with the above three phases at 1230° C and 1.4 GPa; phlogopite appears at temperatures more than 80° C below the liquidus. On the other hand, the melt is not saturated with lherzolite minerals in the presence of 5.13 wt % of H2O and crystallizes olivine and phlogopite as liquidus phases; the stability limit of phlogopite is little affected at least by the present variation of H2O content in the absarokite melt. It is suggested that the absarokite magma was segregated from the upper mantle at 1170° C and 1.7 GPa leaving a phlogopite lherzolite as a residual material on the basis of the above experimental results and the petrographical observation that olivine and phlogopite crystallize at an earlier stage of crystallization sequence than clinopyroxene. The contribution of phlogopite at the stage of melting processes is also suggested by the geochemical characteristics that the absarokite is more enriched in Rb, K, and Ba and depleted in Ca and Na than a typical alkali olivine basalt from the same volcanic field.  相似文献   

12.
A dike–vein complex of potassic type of alkalinity recently discovered in the Baikal ledge, western Baikal area, southern Siberian craton, includes calcite and dolomite–ankerite carbonatites, silicate-bearing carbonatite, phlogopite metapicrite, and phoscorite. The most reliable 40Ar–39Ar dating of the rocks on magnesioriebeckite from alkaline metasomatite at contact with carbonatite yields a statistically significant plateau age of 1017.4 ± 3.2 Ma. The carbonatite is characterized by elevated SiO2 concentrations and is rich in K2O (K2O/Na2O ratio is 21 on average for the calcite carbonatite and 2.5 for the dolomite–ankerite carbonatite), TiO2, P2O5 (up to 9 wt %), REE (up to 3300 ppm), Nb (up to 400 ppm), Zr (up to 800 ppm), Fe, Cr, V, Ni, and Co at relatively low Sr concentrations. Both the metapicrite and the carbonatite are hundreds of times or even more enriched in Ta, Nb, K, and LREE relative to the mantle and are tens of times richer in Rb, Ba, Zr, Hf, and Ti. The high (Gd/Yb)CN ratios of the metapicrite (4.5–11) and carbonatite (4.5–17) testify that their source contained residual garnet, and the high K2O/Na2O ratios of the metapicrite (9–15) and carbonatite suggest that the source also contained phlogopite. The Nd isotopic ratios of the carbonatite suggest that the mantle source of the carbonatite was mildly depleted and similar to an average OIB source. The carbonatites of various mineral composition are believed to be formed via the crystallization differentiation of ferrocarbonatite melt, which segregated from ultramafic alkaline melt.  相似文献   

13.
丹池成矿带是我国重要锡多金属成矿带,过去对丹池成矿带成岩成矿研究主要集中在大厂矿田及五圩矿田,而对丹池成矿带北部的芒场矿田岩浆作用时代、源区特征及其成矿性缺少分析。芒场矿田岩浆活动强烈,发育隐伏斑状花岗岩及有关的花岗斑岩脉和隐伏细粒花岗斑岩及有关的白云母花岗斑岩脉。本文分析花岗斑岩脉U-Pb年龄及花岗斑岩脉和白云母花岗斑岩脉主、微量元素组成,以探讨岩浆活动时代、岩浆源区特征及其成矿潜力。芒场矿田花岗斑岩脉锆石U-Pb年龄为89.1±0.9Ma (MSWD=0.9),和丹池成矿带内大厂矿田岩浆活动时代相近,表明丹池成矿带岩浆活动时代都发生于90Ma左右。白云母花岗斑岩脉具高A/CNK比值(2.69～2.88),含高铝硅酸盐矿物白云母及在Th-Rb图上沿S型花岗岩趋势线分布,和大厂矿田S型黑云母花岗岩的特征基本一致,表明其主要为S型花岗岩。花岗斑岩脉形成时代晚于白云母花岗斑岩脉,但其具有更低的SiO_2含量和更高的MgO、Fe_2O_3~T、CaO和TiO_2含量,且在SiO_2与TiO_2、Fe_2O_3~T、Al_2O_3和P_2O_5关系图中分布于不同区域,没有线性变化关系,显示两者不是同一岩浆结晶分异演化形成的,而为不同沉积变质岩部分熔融形成的。白云母花岗斑岩脉富Al_2O_3、K_2O、Rb、Cs、Sn、W、Nb和Ta,在Rb/Ba-Rb/Sr图上位于富粘土源区,为强风化作用形成的富粘土质富稀有金属源区部分熔融形成的产物。华南西部基底发育经强风化作用形成的富粘土质富稀有金属元素沉积变质源区,为华南西南缘大规模锡矿床的形成提供了物质基础。  相似文献   

14.
Fluorine contents in about 300 samples of various types of basalts and related rocks from continental (southwestern U.S.A.; Zaire; Deccan and South Africa) and oceanic regions (Hawaii and Mid-Atlantic Ridge between 23° N and 40° N) were determined by a selective ion-electrode method.Of all of the major components in these basaltic rocks, F shows good correlation only with K2O. It increases regularly from tholeiite to perpotassic basalt on continents, and from tholeiite to nephelinite on Hawaii. In the F-K2O diagram all the basaltic rocks from continents and Hawaii plot between the origin of the coordinate axes and the field of phlogopite in peridotite xenoliths in South African kimberlites. Accordingly, the major proportions of F, K2O and also H2O in these basaltic magmas are derived from phlogopite at the source regions in the upper mantle. On the other hand, F in abyssal tholeiites is relatively higher than that of the other tholeiites at equal K2O content, and it is suggested that most of F, K2O and H2O are derived from pargasites.When it is assumed that the upper mantle phlogopite contains about 10% K2O, 0.4% (0.3–0.5%) F and 4% H2O, H2O content in basaltic magmas from continental including island arc and oceanic island regions can be qualitatively estimated based on their proportions of K2OFH2O. Similarly, H2O content in abyssal basaltic rocks is also estimated on the basis of FH2O in pargasites (Table 2).A suite of Deccan tholeiites shows remarkable F enrichment with increasing K2O due to separation of anhydrous and K-free minerals during fractionation. F in tholeiitic and alkali basalt magmas in Hawaii also increases regularly with K2O during progressive fractionation until the later stages, where rhyodacite and trachyte exhibit a relative decrease owing to the effective subtraction of F-bearing amphibole and apatite in addition to anhydrous minerals.  相似文献   

15.
Mineralogical and geochemical data suggest that chloride components play an important role in the transformation and partial melting of upper mantle peridotites. The effect of KCl on the transformation of hydrous peridotite rich in Al2O3, CaO, and Na2O was examined in experiments aimed at studying interaction between model NCMAS peridotite with H2O-KCl fluid under a pressure of 1.9 GPa, temperatures of 900–1200°C, and various initial H2O/KCl ratios. The experimental results indicate that KCl depresses the solidus temperature of the hydrous peridotite: this temperature is <900°C at 1.9 GPa, which is more than 100°C lower than the solidus temperature (1000–1025°C) of hydrous peridotite in equilibrium with KCl-free fluid. The reason for the decrease in the melting temperature is that the interaction of KCl with silicates prevails over the effect of chloride on the water activity in the fluid. Experimental data highlight the key role of Al2O3 as a component controlling the whole interaction process between peridotite and H2O-KCl fluid. Garnet, spinel, and pargasite-edenite amphibole in association with aluminous orthopyroxene are unstable in the presence of H2O-KCl fluid at a chloride concentration in the fluid as low as approximately 2 wt % and are replaced by Cl-bearing phlogopite (0.4–1.1 wt % Cl). Interaction with H2O-KCl fluid does not, however, affect clinopyroxene and forsterite, which are the Al poorest phases of the system. Chlorine stabilizes phlogopite at relatively high temperatures in equilibrium with melt at temperatures much higher than the solidus (>1200°C). The compositional evolution of melt generated during the melting of model peridotite in the presence of H2O-KCl fluid is controlled, on the one hand, by the solubility of the H2O-KCl fluid in the melt and, on the other hand, by phlogopite stability above the solidus. At temperatures below 1050°C, at which phlogopite does not actively participate in melting reactions, fluid dissolution results in SiO2-undersaturated (35–40 wt %) and MgO-enriched (up to 45 wt %) melts containing up to 4–5 wt % K2O and 2–3 wt % Cl. At higher temperatures, active phlogopite dissolution and, perhaps, also the separation of immiscible aqueous chloride liquid give rise to melts containing >10 wt % K2O and 0.3–0.5 wt % Cl. Our experimental results corroborate literature data on the transformation of upper mantle peridotites into phlogopite-bearing associations and the formation of ultrapotassic and highly magnesian melts.  相似文献   

16.
东北黑龙江小古里河-科洛-五大连池-二克山火山岩带是我国近代保存最好的火山群之一,此带火山岩的岩石化学特点全都强碱富钾,K2O/Na2O>1.2,属于一套高钾过碱性火山岩。通过对东北钾质火山岩及金云母橄榄岩地幔捕虏体中钾质矿物金云母、白榴石的成分、结晶环境与岩浆成分及来源关系的研究,认为在岩石圈伸展构造背景下,地幔金云母橄榄岩的低度部分熔融形成钾质岩浆,钾质岩浆上升到地壳浅部经历了白榴石的结晶作用。岩浆演化晚期,因钾质矿物大量晶出导致岩浆相对富钠而出现他形霞石和方钠石等填隙矿物。火山岩及地幔捕虏体中富挥发分矿物金云母、白榴石、磷灰石、霞石和方钠石还提供了钾质岩浆富含H2O、F、Cl、P等挥发分的证据。  相似文献   

17.
Occurrence of carbonatite is reported from the Munnar area, Kerala, where an alkali granite-syenite-carbonatite association is seen emplaced along the intersection zone of the Attur and Kerala fault-lineaments. The carbonatites are of two varieties, a calcite-rich sovite and a very coarse grained, calcite and dolomite bearing alvikite. Higher levels of SiO2, Al2O3 and CaO are characteristic of these as compared to the composition of typical carbonatites. The transition element levels are high whereas the incompatible elements show lower values. The low Sr values, lower amount of apatite and absence of rare metal minerals preclude a primary carbonatite magma. The associated syenite and alkali granite have higher K2O, K2O/Na2O, K/Rb, K/Ba and transition element levels. Petrochemical features suggest the rock association to be a result of separation of an immiscible fraction of less viscous carbonate liquid during cooling and ascent from a more viscous polymerized alkali silicate phase. The pre-requisites for melt equilibration and liquid immiscibility were achieved through volatile degassing related to crustal warping and rifting. The unique alkaline association of Munnar, which shows spatial relationships with deep-seated faults as well as a probable triple-point junction, is suggested to be a signature of late Precambrian alkaline magmatism which manifested in the Indian shield as a precursor to the rifting of the continental margin.  相似文献   

18.
胶东招掖郭家岭型花岗岩锆石SHRIMP年代学研究   总被引：48，自引：1，他引：47       下载免费PDF全文
关康 《地质科学》1998,33(3):318-328
采用世界上最先进的SHRIMP锆石U-Pb测年技术,对招掖地区郭家岭型花岗岩及成矿后花岗斑岩脉进行了年代学研究,精确地测定了郭家岭型花岗岩的年龄为130-126Ma,成矿后花岗斑岩脉的年龄为120±2Ma,金矿化被限定在126-120Ma之间。结合岩体年龄和与金矿化密切的空间关系及地球化学上的亲缘关系,认为郭家岭型花岗岩属造山晚期花岗岩,金矿化主要与郭家岭型花岗岩有关。该花岗岩异常高的Ba、Sr含量可作为太古宙绿岩地体环境下判别与金矿化有关花岗岩的地球化学标志。  相似文献   

19.
The magmatic oxygen fugacity (fO2) of a thirty foot wide feldspathic peridotite dyke has been determined using the experimental method of Fudali (1965). Determinations were made on samples from both the marginal and central portions of the dyke and a difference of approximately one order of magnitude in fO2 was observed. This difference is attributed to the increase in the H2O content of the liquid as crystallization proceeded and to diffusion of hydrogen out of the dyke. It is concluded that the dyke was emplaced with an fO2 between 10–8 and 10–9 atmospheres. Data on the absorbtion of Fe by the silver/palladium sample containers during the experiments are given in an appendix.  相似文献   

20.
The paper discusses the mineralogy and geochemistry of altered rocks associated with calcite and dolomite–ankerite carbonatites of the Onguren dyke–vein complex in the Western Transbaikal Region. The alteration processes in the Early Proterozoic metamorphic complex and synmetamorphic granite hosting carbonatite are areal microclinization and riebeckitization; carbonates, phlogopite, apatite, and aegirine occur in the near-contact zones of the dolomite–ankerite carbonatite veins; and silicification is displayed within separated zones adjacent to the veins. In aluminosilicate rocks, microclinization was accompanied by an increasing content of K, Fe3+, Ti, Nb (up to 460 ppm), Th, Cu, and REE; Na, Ti, Fe3+, Mg, Nb (up to 1500 ppm), Zr (up to 2800 ppm), Ta, Th, Hf, and REE accumulated in the inner zone of the riebeckitization column. High contents of Ln Ce (up to 11200 ppm), U (23 ppm), Sr (up to 7000 ppm), Li (up to 400 ppm), Zn (up to 600 ppm), and Th (up to 700 ppm) are typical of apatite–phlogopite–riebeckite altered rock; silicified rock contains up to (ppm): 2000 Th, 20 U, 13000 Ln Ce, and 5000 Ва. Ilmenite and later rutile are the major Nb carriers in alkali altered rocks. These minerals contain up to 2 and 7 wt % Nb2O5, respectively. In addition, ferrocolumbite and aeschynite-(Ce) occur in microcline and riebeckite altered rocks. Fluorapatite containing up to 2.7 wt % (Ln Ce)2O3, monazite-(Ce), cerite-(Ce), ferriallanite-(Ce), and aeschynite-(Ce) are the REE carriers in riebeckite altered rock. Bastnäsite-(Ce), rhabdophane-group minerals, and xenotime-(Y) are typical of silicified rock. Thorite, monazite-(Ce), and rhabdophane-group minerals are the Th carriers.  相似文献   

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