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1.
A new method for primary evaluation of REE ore is based on classification of REE by the level of demand from industry. For their primary evaluation, it is proposed to use an outlook coefficient (Koutl) for REE ores, which is a ratio of the relative amount of critical REE to the relative amount of excess REE: Koutl= (Nd + Eu + Tb + Dy + Er + Y)/REE sum: (Ce + Ho + Tm + Yb + Lu)/REE sum. The use of this coefficient for comparison of REE ores pertaining to various genetic types makes it possible not only to grade newly discovered deposits at the early stage of their study but also to evaluate a possible contribution of well-known deposits, including those currently mined, to output of REE.  相似文献   

2.
Experiments were conducted to evaluate the impact of organic complexation on the development of Ce anomalies and the lanthanide tetrad effect during the adsorption of rare-earth elements (REE) onto MnO2. Two types of aqueous solutions—NaCl and NaNO3—were tested at pH 5 and 7.5. Time-series experiments indicate that a steady-state is reached within less than 10 h when REE occur as free inorganic species, whereas steady state is not reached before 10 d when REE occur as REE-humate complexes. The distribution coefficients (KdREE) between suspended MnO2 and solution show no or only very weak positive Ce anomaly or lanthanide tetrad effect when REE occur as humate complexes, unlike the results obtained in experiments with REE occurring as free inorganic species. Monitoring of dissolved organic carbon (DOC) concentrations show that log KdREEorganic/KdDOC ratios are close to 1.0, implying that the REE and humate remain bound to each other upon adsorption. Most likely, the Ce anomaly reduction/suppression in the organic experiments arises from a combination of two processes: (i) inability of MnO2 to oxidize Ce(III) because of shielding of MnO2 surfaces by humate molecules and (ii) Ce(IV) cannot be preferentially removed from solution due to quantitative complexation of the REE by organic matter. We suggest that the lack of lanthanide tetrad effect arises because the adsorption of REE-humate complexes onto MnO2 occurs dominantly via the humate side of the complexes (anionic adsorption), thereby preventing expression of the differences in Racah parameters for 4f electron repulsion between REE and the oxide surface. The results presented here explain why, despite the development of strongly oxidizing conditions and the presence of MnO2 in the aquifer, no (or insignificant) negative Ce anomalies are observed in organic-rich waters. The present study demonstrates experimentally that the Ce anomaly cannot be used as a reliable proxy of redox conditions in organic-rich waters or in precipitates formed at equilibrium with organic-rich waters.  相似文献   

3.
Partition coefficients for the rare earth elements (REE) Ce, Sm and Tm between coexisting garnets and hydrous liquids have been determined at high pressure and temperatures (30 kbar and 1300 and 1500°C). Two synthetic systems were studied, Mg3Al2Si3O12-H2O and Ca3Al2Si3O12-H2O, in addition to a natural pyrope-bearing system.Deviations from Henry's Law behaviour occur at geologically relevant REE concentrations. At concentrations < 3 ppm Ce, < 12 ppm Sm, < 80 ppm Tm in pyrope and < 100 ppm Ce, < 250 ppm Sm, < 1000 ppm Tm in grossular (at 30 kbar and 1300°C), Dgarnet liquidREE increases as the REE concentration in the garnet decreases. At higher concentrations, DREE is constant. Dgrossular liquidREE also constant when the garnet contains less than about 2 ppm Sm or Tm. The REE concentration at which DREE becomes constant increases with increasing temperature, decreasing REE ionic radius and increasing Ca content of the garnet.Partitioning behaviour of Ce, Sm and Tm between a natural pyrope-rich garnet and hydrous liquid is analogous to that in the synthetic systems and substantiates the substitution model proposed by Harrison and Wood (1980).Values of DREEgarnet/liquid for which Henry's Law is obeyed are systematically higher for grossular than for pyrope (Dpyrope/liquid = 0.067(Ce), 0.108(Sm), 0.155(Tm) and Dgrossular/Liquid = 0.65(Ce), 0.75(Sm), 4.55(Tm).The implications of non-Henry's Law partitioning of REE for models of basalt petrogenesis involving garnet are far-ranging. Deviations from Henry's Law permit refinements to be made to calculated REE abundances once basic model parameters have been defined.  相似文献   

4.
A new mineral species, named naquite(FeSi), is found in the podiform chromitites of the Luobusha ophiolite in Qusong County, Tibet, China. The detailed composition is Fe 65.65, Si 32.57 and Al 1.78 wt%. The mineral is cubic, space group P213. The irregular crystals range from 15 to 50 μm in diameter and form an intergrowth with luobusaite. Naquite is steel grey in color, opaque, with a metallic lustre and gives a grayish-black streak. The mineral is brittle, has a conchoidal fracture and no apparent cleavage. The estimated Mohs hardness is 6.5, and the calculated density is 6.128 g/cm3. Unit-cell parameters are a 4.486 (4) ?, V 90.28 (6) ?3, Z=4. The five strongest powder diffraction lines [d in ? (hkl) (I/I0)] are: 3.1742 (110) (40), 2.5917(111) (43), 2.0076 (210) (100), 1.8307 (211) (65), and 1.1990 (321) (36). Originally called ‘fersilicite’, the species and new name have now been approved by the CNMNC (IMA 2010–010).  相似文献   

5.
Fluorite can be used as a probe for the source of Sr and REE, as well as for the Sr and Nd isotope systematics of mineralizing solutions, allowing characterization of the composition, oxidation state and sources of the fluids. The 87Sr / 86Sr ratios in vein fluorite from the Santa Catarina Fluorite District, southern Brazil, are low (0.720 to 0.745) relative to those of the majority of host granites at the time of mineralization (90 Ma), but are similar to those of less abundant and less evolved Sr- and Ca-rich granites and plagioclases of the heterogeneous Pedras Grandes granite association. Major contributions of Sr from the unradiogenic Parana Basin rocks (87Sr / 86Sr90 Ma = 0.705 to 0.718) are unlikely, considering the radiogenic character of the lower 87Sr / 86Sr end-member in fluorite mixing lines. Estimated fluorite fluid partition coefficients (KdSr-Ca = 0.019 and DSr ≈ 600) indicate a Sr / Ca ratio in the fluorite-forming solution of 0.012, and Sr contents of 0.05 to 0.25 ppm, which are similar to those of present-day granitic geothermal waters. Initial Nd isotopic compositions of the vein fluorites (0.5120 to 0.512) are similar to those of the Pedras Grandes granites. The 143Nd / 144Nd90 Ma of the evolved granites of the Tabuleiro granite association, their accessory fluorites and the Parana Basin rocks are considerably more radiogenic (0.5120 to 0.5127) and these are thus considered to be unlikely sources of the fluids. The REE patterns of vein fluorites, normalized to upper continental crust, show a range of LREE-depleted patterns, with highly variable positive and negative Eu anomalies. The host Pedras Grandes granites show flat to slightly depleted UCC normalized LREE patterns with strong negative Eu anomalies. Depletion of the LREE in fluorites resulted from the mobility of HREE fluoride complexes during fluid migration. A REE fractionation model based on ionic potential ratios indicates that Eu3+ was stable during fluid migration and fluorite precipitation. The coexistence of pyrite and Eu3+ in the mineralizing fluids is consistent with low pH and oxygen fugacities near the hematite-magnetite buffer.  相似文献   

6.
Trace element profiles for common divalent cations (Sr, Zn, Ba), rare-earth elements (REE), Y, U, and Th were measured in fossil bones and teeth from the c. 25 ka Merrell locality, Montana, USA, by using laser-ablation ICP-MS. Multiple traverses in teeth were transformed into 2-D trace element maps for visualizing structural influences on trace element uptake. Trace element compositions of different soils from the fossil site were also analyzed by solution ICP-MS, employing progressive leaches that included distilled H2O, 0.1 M acetic acid, and microwave digestion in concentrated HCl-HNO3. In teeth, trace element uptake in enamel is 2-4 orders of magnitude slower than in dentine, forming an effective trace element barrier. Uptake in dentine parallel to the dentine-enamel interface is enhanced by at least 2 orders of magnitude compared to transverse, causing trace element “plumes” down the tooth core. In bone, U, Ba and Sr are nearly homogeneous, implying diffusivities ∼5 orders of magnitude faster than in enamel and virtually complete equilibration with host soils. In contrast all REE show strong depletions inward, with stepwise linear segments in log-normal or inverse complementary error function plots; these data require a multi-medium diffusion model, with about 2 orders of magnitude difference in slowest vs. fastest diffusivities. Differences in REE diffusivities in bone (slow) vs. dentine (fast) reflect different partition coefficients (Kd’s). Although acid leaches and bulk digestion of soils yield comparable fossil-soil Kd’s among different elements, natural solutions are expected to be neutral to slightly basic. Distilled H2O leachates instead reveal radically different Kd’s in bone for REE than for U-Sr-Ba, suggest orders of magnitude lower effective diffusivities for REE, and readily explain steep vs. flat profiles for REE vs. U-Sr-Ba, respectively. Differences among REE Kd’s and diffusivities may explain inward changes in Ce anomalies. Acid washes and bulk soil compositions yield misleading Kd’s for many trace elements, especially the REE, and H2O-leaches are preferred. Patterns of trace element distributions indicate diagenetic alteration at all scales, including enamel, and challenge the use of trace elements in paleodietary studies.  相似文献   

7.
The competitive binding of rare earth elements (REE) to purified humic acid (HA) and MnO2 was studied experimentally using various HA/MnO2 ratios over a range of pH (3 to 8). MnO2, humic acid and REE solutions were simultaneously mixed to investigate the kinetics of the competitive reactions. Aqueous REE–HA complex is the dominant species whatever the experiment time, pH and HA/MnO2 ratio. The value of the distribution coefficients between MnO2 and solution (log KdRee/Mno2) increases with the HA/MnO2 ratio, indicating that part of the REE–HA complexes are adsorbed onto MnO2. The development of a Ce anomaly appears strongly limited in comparison with inorganic experimental conditions. Throughout the experimental run time, for HA/MnO2 ratios of less than 0.4, MnO2 acts as a competitor leading to a partial dissociation of the REE–HA complex. The majority of the dissociated REE is readsorbed onto the MnO2 surface. The readsorption of REE is expressed by an increased Ce anomaly on the log KdRee/Mno2 pattern as well as a change in shape of the coefficient distribution of REE between soluble HA and solution pattern (log KdRee/HA decrease for the heavy rare earth elements — HREE). Thus, REE are not only bound to MnO2 as a REE–HA complex, but also as REE(III). Moreover, the competition between HA and MnO2 for REE binding is shown to be higher at low pH (< 6) and low DOC/Mn ratio. This study partially confirms previous work that demonstrated the control of REE adsorption by organic matter, while shedding more light on the impact of pH as well as complexation reaction competition on long-term REE partitioning between solid surface and organic solutions. The latter point is important as regards to REE speciation under conditions typical of rock and/or mineral alteration.  相似文献   

8.
High-pressure equilibrium studies were conducted in piston-cylinder apparatus to determine rare earth element (REE) partitioning between garnet and H2O-vapor-saturated liquidus, from 20 kbar/980°C to 30 kbar/1060 °C. Ag capsules were employed to eliminate loss of Fe. Partition coefficients (KD's) were determinined with autoradiographic techniques employing beta-active isotopes of Ce, Sm, and Tm. Major elements in garnet were determined by microprobe analysis. Synthesis and reversal runs of 24 hr or greater duration were used to bracket values of KD's within analytical uncertainty.The KD values for all three REE are constant over the radiogenic concentration range of 1 to 350 ppm, suggesting that the high abundance of natural REE in the starting materials may suppress possible deviations from Henry's Law behavior reported in similar autoradiographic studies of synthetic systems with no natural REE. Changes in KD with increasing pressure and temperature at near-liquidus conditions suggest that the dominant control of KD is the average size of cations occupying the 8-fold sites in garnet. Specifically, the substitution of 8-fold Ca for Mg and Fe causes an increase in KD values greater than that attributable to the coincident effects of pressure and temperature. The inverse correlation of increasing KD with REE ionic radius supports the interpretation that the average size of the 8-fold cation controls the relative variation of KD among REE.These experimental KD values produce less relative fractionation in melts between light REE and heavy REE than do previous KD's derived from data on coexisting natural garnet phenocryst/rockmatrix pairs. Models for the derivation of orogenic andesites from partial melting of subducted basaltic eclogite are qualitatively improved by these new KD's. Existing calculations of KD values necessary for the viability of the eclogite fractionation are also in good agreement with these experimental KD values.  相似文献   

9.
Microhardness (H) and fracture toughness (K 1C) have been studied for the main varieties of shock-resistant cryptocrystalline fluorite, a natural ceramic widespread at the Suran deposit. Suran cryptocrystalline fluorite (SCF) is characterized by high fracture toughness (K 1C), which is 2–5 times higher than K 1C of common fluorite monocrystals. The relationship between K 1C and microhardness H is complex and nonlinear. The SCF varieties from the sellaite-fluorite orebody are distinguished by the highest K 1C = 1.9–2.3 MPa m1/2, which exceeds K 1C = 0.84 MPa m1/2 of porcelain-like fluorite from the main fluorite orebody. Qualitative and quantitative variations of structural point defects in the studied samples exert a much stronger effect on microhardness than on fracture toughness, which mainly depends on the size of crystallites, their mutual crystallographic orientation, and the structure of intergranular boundaries, i.e., on the parameters seemingly related to recrystallization and/or twinning of fluorite. In general, the nature of the Suran deposit of fluorite ceramic with unusual physicomechanical properties remains a geological puzzle in many respects.  相似文献   

10.
Usually it is assumed that the partitioning of trace elements into titanite in metaluminous granitoid plutonic environments takes place under equilibrium conditions and that compositional zoning is due solely to progressive changes in melt chemistry and/or mineral/melt partition coefficients. Examination of titanites from a variety of Caledonian metaluminous granitoids and related rocks has revealed that sector zoning is present, indicating disequilibrium partitioning. The sector zoning in titanites is defined principally by the distribution of the rare earth elements (REE), Y, Nb, Al and Fe. The REE, Y and Nb preferentially occur within the minor (100) sectors relative to the morphologically important (111) sectors. The reverse is true of Al and Fe which preferentially occur within the (111) sectors relative to the (100) sectors. The patterns of sector zoning are complicated by the fact that the relative growth rates of the various crystal faces fluctuated during growth. Sector zoning indicates that crystal-interface kinetics are responsible for the observed patterns of element partitioning. It is concluded that differences in the lateral-layerspreading rates of crystal faces bring about the sector zoning. The results have implications for the use of trace element partition coefficients in the modelling of fractionation processes.  相似文献   

11.
The South Platte pegmatite district is well known for its significant enrichment in the rare earth elements (REE), Y, Nb, F, and for the exceptionally well-developed internal zonation of the complex pegmatites located within a reversely zoned portion of the Pikes Peak batholith. Chemical trends both within and between pegmatites define the behavior of major and trace elements and the role of F in the fractionation of the granitic magma and pegmatitic fluids, suggesting a new model for the evolution of the granite-pegmatite system.Whole-rock XRF and INAA analyses of the host Pikes Peak granite and quartz monzonite and pegmatite wall zones provide strong evidence that all three are related by differentiation. With increasing SiO2, there is systematic enrichment in K2O, Na2O, and Rb, and depletion in CaO, MgO, FeO1, TiO2, P2O5, Ba, Sr, and Sc. REE, Y, Zr, and Th were strongly partitioned out of the wall zone into the final residual fluids where they were concentrated up to an order of magnitude over levels in the granite.Within the district, there is also chemical zonation of F, Nb, Th, U, and REE between groups of pegmatites. Polyzonal quartz-core types typically contain more fluorite, samarskite, HREE-zircon, and yttrian-fluorite than their bizonal composite-core counterparts, which contain only sparse fluorite and allanite.The sequence of magmatic evolution involved: (1) a process of diffusive differentiation and fractional crystallization which produced a chemically stratified magma chamber with a hotter more mafic quartz monzonitic base and a more felsic, granitic top enriched in H2O, F, HREE, Nb, and Y; (2) resurgence of the more mafic lower level crystal mush in to the upper more felsic part of the pluton; and (3) separation of pegmatitic fluids from the juxtaposed magmas giving rise to two compositionally distinct groups of pegmatites.  相似文献   

12.
The giant Bayan Obo REE–Nb–Fe deposit consists of replacement bodies hosted in dolomite marble made up of magnetite, REE fluorocarbonates, fluorite, aegirine, amphibole, calcite and barite. Two or three phase CO2-rich, three phase hypersaline liquid–vapor–solid, and two phase liquid-rich inclusions have been recognized in mineralized fluorite and quartz samples. Microthermometry measurements indicate that the carbonic phase in CO2-rich inclusions is nearly pure CO2. Fluids involving in REE–Nb–Fe mineralization at Bayan Obo might be mainly of H2O–CO2–NaCl–(F–REE) system. Coexistences of brine inclusions and CO2-rich inclusions with similar homogenization temperatures give evidence that immiscibility happened during REE mineralization. An unmixing of an original H2O–CO2–NaCl fluid probably derived from carbonatitic magma. The presence of REE-carbonates as an abundant solid in fluid inclusions shows that the original ore-forming fluids are very rich in REE, and therefore, have the potential to produce economic REE ores at Bayan Obo.  相似文献   

13.
The Silius vein system, located in SE Sardinia (Italy) is analogous to other late- to post-Hercynian mineral systems of this type in Europe. The Silius system consists of two main veins, characterized by several generations of fluorite, calcite and quartz, with initial ribbon-like geometries, followed by breccias and cockade-like textures. In this study, aimed at investigating the REE concentrations in the Silius vein system, a REE average of ~ 800 ppm (locally ΣREE > 1500 ppm) has been observed in the carbonate gangue of the fluorite orebody. These amounts are related to the presence of the REE-bearing minerals synchysite-(Ce) and xenotime-(Y). The chemical composition of synchysite-(Ce) has been obtained by wavelength dispersive spectrometry (WDS). The average synchysite-(Ce) formula, built on the basis of (CO3)2F and 5 negative charges, is Ca1.07(La0.19,Ce0.36,Pr0.04,Nd0.15,Sm0.03,Gd0.03,Y0.13)(CO3)2F. From their geochemical characteristics, and their textural relationships with other gangue phases, it is likely that synchysite-(Ce) and xenotime-(Y) formed at the same P-T-X conditions as the other minerals of the Silius fluorite mineralization. Synchysite-(Ce) and xenotime-(Y) at Silius could be related to a local circulation phenomenon, where the REE are derived from a REE-bearing source rock in the basement of southeastern Sardinia, which has been leached by the same fluids precipitating the fluorite/calcite mineralization. REE concentrations contained in the carbonate gangue of still unexploited parts of the Silius vein deposit, as well as in dumps and tailings accumulated during past fluorite processing, could possibly represent a sub-economic by-product of the fluorite exploitation.  相似文献   

14.
在野外地质调查的基础上,结合室内显微镜观察及电子探针分析测试,对新疆拜城波孜果尔碱性岩中的副矿物的矿物学特征和化学成分进行了研究.发现这些副矿物常以共生组合的形式产在碱性岩中,主要分布在石英二长闪长岩和石英二长岩中.烧绿石中U、Th和REE替代Ca、Na.独居石富含LREE,Th和LREE相互替代;根据独居石中w(La+ Ce) ＞40％和La/Nd比值在1.6～4.5,推断独居石为热液成因.磷钇矿中富含REE,且以HREE为主;w(Th)＞w(U).锆石中Zr/Hf比值在60％以上,符合碱性岩特征;其Th/U比值为0.6,属于岩浆锆石.星叶石中w(Rb2O)、w(Cs2O)较高.萤石中Y、Ce替代Ca.锆石中的钍石w(U)明显高于磁铁矿中钍石w(U).在石英二长岩中,烧绿石的w(CaO)、w(TiO2)、w(ZrO2)、w(U3O8),磷钇矿的w(Y2O3),星叶石的w(TiO2),萤石的w(Ca),氟碳铈镧矿的w(CaO)较丰富;而在石英二长闪长岩中,烧绿石的w(Ce2O3),磷钇矿的REE含量,星叶石的w(Nb2O5)、w(Rb2O),萤石w(Ce)、w(Y)和氟碳铈镧矿的w(La2O3)较高.  相似文献   

15.
The Vergenoeg fluorite deposit in the Bushveld Complex in South Africa is hosted by a volcanic pipe-like body. The distribution characteristics, composition and formation conditions of high-field-strength element (HFSE)-rich minerals in different lithological units of the deposit were investigated by optical and cathodoluminescence microscopy, scanning electron microscopy, X-ray fluorescence, inductively-coupled plasma mass-spectrometry and electron-probe microanalysis. The Vergenoeg host rocks comprise a diverse silica-undersaturated assemblage of fayalite–magnetite–fluorite with variably subordinate apatite and mineral phases enriched in rare-earth elements (REEs). The Sm–Nd isotope systematics of the fluorite from the various lithological units of the pipe support the model that the HFSE budget of the Vergenoeg pipe was likely derived from a Lebowa-type granitic magma. Isotopically, there is no evidence for other REE sources. Formation of the pipe, including development of the fluorite mineralization, occurred within the same time frame as the emplacement of other magmatic rock units of the Bushveld Complex (Sm–Nd isochron age for fluorite separates: 2040 ± 46 Ma). Hydrothermal alteration is manifested in strongly disturbed Rb–Sr isotope systematics of the Vergenoeg deposit, but did not affect its HFSE and REE budget. Whole-rock chondrite-normalized REE + Y distribution patterns of two types were observed: (i) flat patterns characteristic of magnetite–fluorite unit, gossan, metallurgical-grade fluorite (“metspar”) plugs and siderite lenses, and (ii) U-shaped patterns showing enrichment towards the heaviest REE (Tm–Lu) observed in the fayalite-rich units. Common HFSE minerals are complex Nb-rich oxides (samarskite, fergusonite), REE phosphates and fluorocarbonates. Additionally, fluocerite and REE silicates, whose identification requires further work, were found. Most of the HFSE-rich minerals are spatially associated with Fe-rich phases (e.g., pyrite, magnetite, greenalite and hematite). To a smaller extent, they are found finely disseminated or healing micro-fractures in fluorite. The whole-rock REE + Y distribution patterns of the individual lithological units are mainly controlled by the distribution of Yb-rich and Y-rich xenotime in these rocks. The common occurrence of bastnäsite-(Ce) in the gossan, “metspar” plugs and especially in the rhyolitic carapace at the pipe–wall-rock contact, controls the REE + Y distribution patterns of these rocks. HFSE minerals in the Vergenoeg pipe rocks have formed in several stages. Samarskite and coarse fluorapatite belong to the primary mineral assemblage. Fergusonite and Yb-rich xenotime formed during high- to moderate-temperature hydrothermal activity. Significant remobilization of the HFSE from the early-crystallized minerals (breakdown of fluorapatite and possibly allanite with release of REE + Y) and subsequent partial redistribution of these elements into near surface rocks are inferred. The late-stage assemblages are characterized by the presence of fine-grained REE fluorocarbonates, monazite-(Ce), monazite-(La) and xenotime-(Y).  相似文献   

16.
Using our database of the compositions of melt inclusions and quenched glasses of basaltic magmas from mid-ocean ridges (MORB), the average concentrations and ratios of H2O, Cl, F, S, K2O, Ce, and Dy were determined in these magmas. Assuming that the concentration ratios of volatile components to K2O are constant in the MORB magmas and their sources (depleted mantle, DM), and taking an average K2O content in the DM of 72 ppm, the following average contents were estimated for the DM: 158 ppm H2O, 6.6 ppm Cl, and 8.3 ppm F. Using an S/Dy ratio of 212 for MORB melts and a Dy concentration of 0.531 ppm in the DM, the concentration of S in the DM was estimated as 113 ppm. Our value for the average content of Cl is much higher than estimates obtained by other authors. This discrepancy could be due either to the assimilation of crustal (and hydrospheric) Cl by MORB magmas or to the deep mantle recycling of Cl. The latter mechanism is supported by the statistically significant positive correlation of Cl with K2O, H2O, and F. Such a correlation is not consistent with the hypothesis of basaltic magma contamination by seawater-derived chloride brines. Similar to other surface processes, the assimilation of crustal material operates within the existing global correlations and disturbs them. Based on the average integrated degree of mantle melting and the average degree of MORB magma differentiation (0.05), the average contents of potassium and volatile components in N-MORB and E-MORB mantle sources were estimated as 39 and 126 ppm K2O, 103 and 197 ppm H2O, 4.0 and 10.7 ppm Cl, and 3.9 and 9.1 ppm F, respectively. It is not likely that normal MORB magmas can be derived from depleted mantle that experienced a previous partial melting event (for instance, during the extraction of the primordial continental crust in the Early Precambrian), which was referred to as the ultradepleted mantle. Ordinary (not ultradepleted) MORB magmas can be derived either by the melting of a zone enriched DM (for instance, progressively enriched in incompatible components with depth), which is hardly possible, or by the continuous addition (mixing) of an enriched component to the ultradepleted mantle at the expense of sediments and crustal materials involved in deep recycling.  相似文献   

17.
Magnetite-Fluorite Rock:A New Rock Type of Hot Water Sedimentation   总被引：2，自引：0，他引：2  
The new type hot water sedimentary rock -- magnetite-fluorite rock occurs as quasi-layers in flat parts of contact zones between rock body and strata in Bamianshan of Changshan County, Zhejiang Province, China. The main mineral assemblage is fluorite＋magnetite＋cassiterite. The rock shows typical laminated structure and obvious mosaic texture. Its formation temperature is between 123℃-160℃, averaging at 142℃. The major chemical composition of the rock includes CaF2, SiO2, Al2O3, FeO, and Fe2O3; the high-content microelement association includes W, Sn, Be, Rb, Sr, S, and CI; and the total content of REE is low （∑REE between 35.34×10^-6-38.35×10^-6）, showing LREE enrichment type of distribution pattern. Diagenesis： driven by the tectonic stress, the formation water heated in the deep strata had moved along the fissures or fractures in strata and had extracted components from the strata on the way, and finally stagnated in the flat parts of contact zones between rock body and strata. With drop in temperature, magnetite and fluorite were separated from the hot water and precipitated alternately, forming this hot water sedimentary rock with new type mineralogical composition, typical laminated structure, obvious mosaic texture and sub-horizontal occurrence. The characteristics of the new type mineralogical composition, sedimentary tectonic environment and chemical composition are different from that of the well-known traditional hydrothermai sedimentary rocks.  相似文献   

18.
Distributions of the rare-earth elements (REE) in omphacite and garnet and REE behaviors during metamorphic processes were discussed. The REE concentrations of garnet and omphacite in six eclogite samples from the Dabie Mountain, central China, were measured by inductively coupled plasma-mass spectrometry (ICP-MS). The correlation of δEu ratios between garnet and omphacite indicated that chemical equilibrium of REE distribution between garnet and omphacite could be achieved during ultra-high pressure (UHP) metamorphism. Most of the partition coefficients (Kd=CiOmp/CiGrt) of light rare-earth elements (LREE) are higher than 1. However the partition coefficients of heavy rare-earth elements (HREE) are lower than 1. This indicated that the LREE inclined to occupy site M2 in omphacite, but the HREEs tended to occupy eightfold coordinated site in garnet during the eclogite formation. The REE geochemistry of the eclogites indicated that LREE could be partially lost during the prograde metamorphic process of protolith, but be introduced into the rocks during the symplectite formation. LREE are more active than HREE during the UHP metamorphism. The results are favorable to highlighting the REE behavior and evolution of UHP metamorphic rocks.  相似文献   

19.
The Gardar failed-rift Province is world-famous for its (per-)alkaline plutonic rocks. Elevated contents of F in the mantle source and F-enrichment in the parental melts have been suggested to account for the peculiarities of the Gardar rocks (e.g. their rare mineralogy, extreme enrichment of HFSE elements, Be or REE in the Ilímaussaq agpaites, and the formation of the unique Ivigtut cryolite deposit). To constrain the formation and chemical evolution of F-bearing melts and fluids, fluorides (fluorite, cryolite, villiaumite, cryolithionite), calcite and siderite from the Ilímaussaq, Motzfeldt and Ivigtut complexes were analysed for their trace element content focusing on the rare earth elements and yttrium (REE).The various generations of fluorite occurring in the granitic Ivigtut, agpaitic Ilímaussaq and miaskitic to agpaitic Motzfeldt intrusions all share a negative Eu anomaly which is attributed to (earlier) feldspar fractionation in the parental alkali basaltic melts. This interpretation is supported by the abundance of anorthositic xenoliths in many Gardar plutonic rocks.The primary magmatic fluorites from Ilímaussaq and Motzfeldt display very similar REE patterns suggesting a formation from closely related parental melts under similar conditions. Hydrothermal fluorites from these intrusions were used to constrain the multiple effects responsible for the incorporation of trace elements into fluorides: temperature dependence, fluid migration/interaction and complexation resulting in REE fractionation. Generally, the REE patterns of Gardar fluorides reflect the evolution and migration of a F/CO2-rich fluid leading to the formation of fluorite and fluorite/calcite veins. In certain units, this fluid inherited the REE patterns of altered host rocks. In addition, there is evidence of an even younger fluid of high REE abundance which resulted in highly variable REE concentrations (up to three orders of magnitude) within one sample of hydrothermal fluorite.The REE patterns of the granitic Ivigtut intrusion show flat to slightly heavy-REE-enriched patterns characterised by a strong tetrad effect. This effect is interpreted to record extensive fluid–rock interaction in highly fractionated, Si-rich systems.Interestingly, the fluorides appear to record different source REE patterns, as the spatially close Motzfeldt and Ilímaussaq intrusions show strong similarities and contrast with the Ivigtut intrusion located 100 km NE. These variations may be attributed to differences in the tectonic position of the intrusions or mantle heterogeneities.  相似文献   

20.
Shock recovery experiments for single crystal and powdered specimens of TiO2 with the rutile structure were performed in the pressure range up to 72 GPa. Single crystal specimens were shocked parallel to [100], [110] and [001] directions. X-ray powder diffraction analysis showed that the amount of -PbO2 type TiO2 produced by shock-loading depended strongly on the shock propagation direction. The maximum yield (about 70%) was observed for shock loading to 36 GPa parallel to the [100] direction. In the [001] shock direction, the yield is much smaller than that of the [100] direction. This anisotropic yield was consistent with the observed anisotropy of the phase transition pressure in shock compression measurements. However, transformation to the -PbO2 type cannot explain the large volume change observed above about 20 GPa. On the basis of the high pressure behavior of MnF2, we assumed that the high pressure phase was either fluorite or distorted fluorite type and that the phase conversion to the -PbO2 type was induced spontaneously in the pressure reduction process.We present a displacive mechanism of phase transition under shock compression from the rutile structure to the fluorite structure, in which the rutile [100] is shown to correspond to the fluorite [001] or [110] and the rutile [001] to the fluorite [110]. Direct evidence is obtained by examining the [100] shocked specimen by high resolution electron microscopy.  相似文献   

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