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1.
The Adamello gabbro exposed on the summit of Cornone di Blumone, Western Alps, Italy, has been fused by lightning strikes to form magnetite-rich fulgurites produced by melting of magnetite, hornblende, calcic plagioclase and minor clinopyroxene. The composition of quench magnetite in the fulgurite is 44.4 Fe3O4; 27.5 MgFe2O4; 15.1 FeAl2O4; 7.9 Fe2TiO4; 2.5 Fe2SiO4; 1.9 CaFe2O4; 0.8 MnFe2O4 and is inferred to have crystallized from a low-Si, Fe-rich melt under high oxidation conditions of about 1 log unit below the log10?O2 of hematite–magnetite. The low Si, Fe-rich melt is considered to have been produced from fusion of magnetite + hornblende-rich areas of the host gabbro and/or possible separation of an immiscible high Fe2O3/FeO Fe-rich, low-Si melt from a more siliceous glass during superheating. Skeletal-dendritic morphologies of magnetite in the fulgurite indicate crystallization under conditions of extreme supercooling. Juxtaposition of areas exhibiting different growth habits and crystal sizes of magnetite may reflect compositionally different local melt domains and/or small differences in the delicate balance between nucleation and growth in domains that had slightly different, although ultrafast, cooling rates.  相似文献   

2.
《Applied Geochemistry》1993,8(2):177-187
The bulk geochemistry of unconsolidated sands from river terraces in two drainage basins of contrasting geology in the Limagne rift valley, France, was studied. Data processing and interpretation was done with multivariate statistics, notably factor analysis. In the Allier drainage basin, underlain by volcanic rocks and crystalline basement, the abundance of basaltic rock fragments causes significantly higher bulk concentrations of TiO2, Al2O3, Fe2O3, MgO, CaO, P2O5, V, Cr, Ni, Zn, Sr, Zr and Nb. In the Dore basin, underlain only by crystalline basement, sands have a significantly higher SiO2, K2O, Rb and Pb content, originating from quartz, K-feldspars and micas. Comparison between different terrace levels shows the impact of weathering and changes in supplied sediment composition over time. Approximately 65% of the total variance in the basaltic element content in the Allier terrace sands can be explained by the combined effect of parent material and weathering. The effect of grain size on sediment composition is only significant for Al2O3, Na2O and Rb content in the Allier sands, and for TiO2, Fe2O3 and Nb content in the Dore sands. Approximately 60% of the total variability in these elements is grain-size related. These results show that the technique of studying the bulk geochemical composition of stream sediments has direct applications for mineral exploration and Quaternary research.  相似文献   

3.
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4.
The Zambales ophiolite is the major source of chromite ore in the Philippines. The chromitites are concordant cumulates and are associated with distinct chromitite-bearing sequences within the mantle peridotites. Refractory and metallurgical chromite deposits are spatially separated and related to different lithologic associations, which crystallized from different parental magmas. — Refractory chromite ores (30–44 wt% Cr2O3; 20–30 wt% Al2O3) are linked with the peridotite-troctolite-olivine gabbro lineage. Two main types were found: (1) Al-rich refractory ores associated with harzburgites and feldspathic periodotites and (2) more Cr-rich varieties associated with lherzolites. — Metallurgical chromite ores (45–53 wt% Cr2O3; 12–18 wt% Al2O3) are linked with the peridotite-pyroxenite-norite lineage. Two main types were also found: (1) Cr-rich metallurgical ores associated with orthopyroxenites and (2) more Al-rich varieties related to clinopyroxenites. — The chemical composition of chromite within the deposits varies depending on the chromite/silicate ratios of the ore types and grades continuously into accessory chrome spinels in the wall-rock peridotites. — The geochemistry of accessory chrome spinels in various peridotites and mafic cumulates depends on the mineralogical composition and the stratigraphic position of their host rocks.New address: BEB Erdgas und Erdöl GmbH, Riethorst 12, D-3000 Hannover 51The terms chrome-spinels and chromite are used as follows: 1. Chrome-spinel is only used for those occuring as accessory minerals in various ultramafic and mafic rocks (= accessory chrome-spinels). Their chemical composition has been determined only by microprobe analysis. — 2. Chromite is used for ore and ore deposits (=chromitites); the chemical composition has been determined by wet chemistry (AAS) or by microprobe analysis  相似文献   

5.
After its initial synthesis as the new compound Mg2Al3B2O9(OH) (Daniels et al. 1997) pseudosinhalite has now been discovered as a new mineral. It occurs, together with hydrotalcite, as a replacement product of sinhalite, MgAlBO4, in an impure marble of the contact metasomatic iron boron deposit of Tayozhnoye in the Aldan Shield of Siberia. Its chemical composition determined by electron microprobe is (wt%): Al2O3 46.88; MgO 25.12; FeO 1.99; B2O3 (calculated) 21.75; H2O (calculated) 2.81 giving a total of 98.55 and leading to the empirical formula (Mg2.00 Fe2+ 0.09)Σ=2.09 Al2.94 B2O9(OH). The small deviation from the ideal stoichiometry with (Mg?+?Fe2+):Al?≠?2:3 may be caused by either solid solution towards, or submicroscopic interlayering with lamellae of, the structurally similar mineral sinhalite. The underlying substitution involving also B and H would be (Mg?+?Fe)+?B=Al+2H. Pseudosinhalite is monoclinic, space group P21/c, with a=7.49(1), b=4.33(1), c=9.85(2) Å; β=110.7(1)°; V?=?299(1) Å3; Z?=?2. Calculated density is 3.508?g/cm3. Pseudosinhalite is colourless with white streak and has a vitreous lustre. It is transparent; no fluorescence was detected. There is no cleavage and parting; fractures are concoidal. Optical constants could not be measured properly due to polysynthetic microtwinning, but α<1.72<γ. For synthetic pseudosinhalite α=1.691(1); β=1.713(1); γ=1.730(1); Δ=0.039; 2?V=80°. The temperature of pseudosinhalite formation was below about 400?°C at low pressures and with a hydrous, CO2-bearing fluid participating in the reaction.  相似文献   

6.
Aqualite, a new eudialyte-group mineral from hydrothermally altered peralkaline pegmatites of the Inagli alkaline pluton (Sakha-Yakutia, Russia) is described in this paper. Natrolite, microcline, eckermanite, aegirine, batisite, innelite, lorezenite, thorite, and galena are associated minerals. Aqualite occurs as isometric crystals up to 3-cm across. The color is pale pink, with a white streak and vitreous luster. The mineral is transparent. The fracture is conchoidal. The mineral is brittle; no cleavage or parting is observed. The Mohs’ hardness is 4 to 5. The density is 2.58(2) g/cm3 (measured by the volumetric method) and 2.66 g/cm3 (calculated). Aqualite is optically uniaxial (+), α = 1.569(1) and β = 1.571(1). The mineral is pleochroic from colorless to pale pink on X and pink on Y, α < β. Aqualite is weakly fluorescent with a dull yellow color under ultraviolet light. The mineral is stable in 50% HCl and HNO3 at room temperature. Weight loss after ignition at 500°C is 9.8%. Aqualite is monoclinic, and the space group is R3. The unit-cell dimensions are a = 14.078(3) Å, c = 31.24(1) Å, V = 5362 Å3, and Z = 3. The strongest reflections in the X-ray powder pattern [d, Å (I)(hkl)] are: 4.39(100)(2005), 2.987(100)(315), 2.850(79)(404), 10.50(44)(003), 6.63(43)(104), 7.06(42)(110), 3.624(41)(027), and 11.43(39)(101). The chemical composition (electron microprobe, H2O determined with the Penfield method) is as follows (wt %): 2.91 Na2O, 1.93 K2O, 11.14 CaO, 1.75 SrO, 2.41 BaO, 0.56 FeO, 0.30 MnO, 0.17 La2O3, 0.54 Ce2O3, 0.36 Nd2O3, 0.34 Al2O3, 52.70 SiO2, 12.33 ZrO2, O.78 TiO2, 0.15 Nb2O5; 1.50 Cl, 9.93 H2O,-O=Cl2 0.34; where the total is 99.46. The empirical formula calculated on the basis of Si + Zr + Ti + Al + Nb = 29 apfu is as follows: [(H3O)7.94Na2.74K1.20Sr0.49Ba0.46Fe0.23Mn0.12]Σ13.18(Ca5.79REE0.19)Σ5.98 (Zr2.92Ti0.08)Σ3.0(Si25.57Ti0.21Al0.19Nb0.03)S26.0[O66.46(OH)5.54]Σ72.0 [(OH)2.77Cl1.23]Σ4.0. The simplified formula is (H3O)8(Na,K,Sr)5Ca6Zr3Si26O66(OH)9Cl. Aqualite differs from typical eudialyte by the extremely low contents of Na and Fe, with more than 50% Na being replaced with the (H3O)+ group. The presence of oxonium ions is confirmed by IR spectroscopic and X-ray single-crystal diffraction analysis. The mineral is compared with five structurally studied high-oxonium analogues from alkaline plutons of other regions. All of these minerals were formed at a relatively low temperature through the ion-exchange transformation of “protoeudialytes”; the successor minerals inherited the principal structural and compositional features of the precursor minerals. The name aqualite is derived from the Latin aqua in reference to its specific chemical composition. The type material of aqualite is deposited in the Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow.  相似文献   

7.
《Applied Geochemistry》2002,17(6):683-698
The compositional variability of the phenocryst-poor member of the 12.8 Ma Topopah Spring Tuff at the potential repository level was assessed by duplicate analysis of 20 core samples from the cross drift at Yucca Mountain, Nevada. Previous analyses of outcrop and core samples of the Topopah Spring Tuff showed that the phenocryst-poor rhyolite, which includes both lithophysal and nonlithophysal zones, is relatively uniform in composition. Analyses of rock samples from the cross drift, the first from the actual potential repository block, also indicate the chemical homogeneity of this unit excluding localized deposits of vapor-phase minerals and low-temperature calcite and opal in fractures, cavities, and faults. The possible influence of vapor-phase minerals and calcite and opal coatings on rock composition at a scale sufficiently large to incorporate these heterogeneously distributed deposits was evaluated and is considered to be relatively minor. Therefore, the composition of the phenocryst-poor member of the Topopah Spring Tuff is considered to be adequately represented by the analyses of samples from the cross drift. The mean composition as represented by the 10 most abundant oxides in wt.% or g/100 g is: SiO2, 76.29; Al2O3, 12.55; FeO, 0.14; Fe2O3, 0.97; MgO, 0.13; CaO, 0.50; Na2O, 3.52; K2O, 4.83; TiO2, 0.11; and MnO, 0.07.  相似文献   

8.
The compositional dependence of the redox ratio (FeO/FeO1.5) has been experimentally determined in K2O-Al2O3-SiO2-Fe2O3-FeO (KASFF) and K2O-CaO-Al2O3-SiO2-Fe2O3-FeO (KCASFF) silicate melts. Compositions were equilibrated at 1,450° C in air, with 78 mol % SiO2. KASFF melts have from 1 to 5 mol % Fe2O3 and include both peraluminous (K2O2O3) and peralkaline (K2O>Al2O3) compositions. KCASFF melts have 1 mol % Fe2O3 encompassing peraluminous, metaluminous (CaO+K2O>Al2O3) and peralkaline compositions. Peralkaline KASFF melts with 1 mol % Fe2O3 have low and constant values for the redox ratio, whereas in peraluminous melts the redox ratio increases with increasing (K2O/Al2O3). Increasing total iron concentration increases the redox ratio in peraluminous melts and slightly decreases the redox ratio in peralkaline melts. Substituting CaO for K2O at fixed total iron (1 mol %) increases the redox ratio in both peraluminous and metaluminous KCASFF melts; however, the redox ratio in peralkaline KCASFF melts is not affected by this exchange. These data indicate that Fe3+ is in four-fold coordination, with K+ or Ca2+ providing local charge balance. The tetrahedral ferric species is most stable in peralkaline melts and least stable in peraluminous melts, due to the competition between Al3+ and Fe3+ for charge balancing cations in the latter melt. Tetrahedral Fe3+ is also less stable when Ca2+ provides local charge balance. The data are consistent with a network modifying role for Fe2+ in the melt.The data are interpreted to reflect the effects of melt composition on the partitioning of K+ and Ca2+ and Fe3+ and Al3+ between various species in the melt. These relationships are discussed in terms of homogeneous equilibria between various iron-bearing and iron-free melt species. The results also reflect the effect of liquid composition on the exchange potentials Fe3+ Al–1 and Ca0.5K–1. The exchange potentials are relatively constant in peralkaline melts, but decrease in metaluminous and peraluminous melts as both (CaO+K2O)/(CaO+K2O+Al2O3) and K2O/CaO decrease. These qualitative observations imply that minerals exhibiting these exchanges will also be similarly affected as liquid composition changes. Present address: Department of Geological Sciences, Virginia Tech, Blacksburg, VA 24061, USA  相似文献   

9.
Crystalline and melt inclusions were studied in large (up to 2 cm across) dipyramidal quartz phenocrysts from Miocene dacites in the area of the Rosia Montana Au-Ag deposit in Romania. Data were obtained on the homogenization of fluid inclusions and the composition of crystalline inclusions and glasses in more than 40 melt inclusions, which were analyzed on a electron microprobe. The minerals identified in the crystalline inclusions are plagioclase (An 51–62), orthoclase, micas (biotite and phengite), zircon, magnetite (TiO2 = 2.8 wt %), and Fe sulfide. Two types of the melts were distinguished when studying the glasses of the melt inclusions. Type 1 of the melts is unusual in composition. The average composition of 20 inclusions is as follows (wt %): 76.1 SiO2, 0.39 TiO2, 6.23 Al2O3, 4.61 FeO, 0.09 MnO, 1.64 MgO, 3.04 CaO, 2.79 Na2O, 3.79 K2O (Na2O/K2O = 0.74), 0.07 P2O5, 0.02 Cl. The composition of type 2 of the melts is typical of acid magmas. The average of 23 inclusion analyses is (wt %) 79.3 SiO2, 0.16 TiO2, 10.27 Al2O3, 0.63 FeO, 0.08 MnO, 0.29 MgO, 1.83 CaO, 3.56 Na2O, 2.79 K2O (Na2O/K2O = 1.28), 0.08 P2O5, 0.05 Cl. The compositions of these melts significantly differ in concentrations of Ti, Al, Fe, Mg, Ca, Na, and K. The high analytical totals of the analyses (close to 100 wt %, more specifically 98.9 and 99.0 wt %, respectively) testify that the melts were generally poor in water. Two inclusions of type 1 and two inclusions of type 2 were analyzed on an ion probe, and their analyses show remarkable differences in the concentrations of certain trace elements. These concentrations (in ppm) are for the melts of types 1 and 2, respectively, as follows: 10.0 and 0.69 for Be, 29.3 and 5.7 for B, 6.4 and 1.4 for Cr, 146 and 6.9 for V, 74 and 18 for Cu, 92 and 29 for Rb, 45 and 15 for Zr, 1.7 and 0.6 for Hf, 10.3 and 2.3 for Pb, and 52 and 1.3 for U. The Th/U ratio of these two melt types are also notably different: 0.04 and 0.19 for type 1 and 2.0 and 2.9 for type 2. These data led us to conclude that the magmatic melts were derived from two different sources. Our data on the melts of type 1 testify that the magmatic chamber was contaminated with compositionally unusual crustal rocks (perhaps, sedimentary, metamorphic, or hydrothermal rocks enriched in Si, Fe, Mg, U, and some other components). This can explain the ore-forming specifics of magmatic chambers in the area.  相似文献   

10.
Scapolite at Mary Kathleen (North-Western Queensland) occurs in calcareous and non-calcareous metapelites, acid and basic metavolcanics and metadolerites. Graphical treatment of the relationship between scapolite composition (Me%) and the host rock oxide ratios CaO/Na2O and Al2O3/(CaO + Na2O) reveals the following points:
  1. The calcareous metapelites are also very sodic.
  2. Scapolite in calcareous metapelites is more marialitic than that in low-calcium equivalents.
  3. In graphs of Me% against CaO/Na2O and Al2O3/(CaO + Na2O) the metasediments and the metaigneous rocks show markedly different trends.
It is concluded that scapolite in the metasediments originated by isochemical metamorphism of shales and marls containing evaporitic halite. The local abundance of halite was the main control on the composition and distribution of the scapolite, but the relative abundance of CaO and Na2O was a modifying factor. In the metaigneous rocks scapolite formed metasomatically during regional metamorphism by the introduction of volatile-rich fluids derived from the adjacent evaporitic sediments. The relative availability of CO2 and Cl2 again appears to have been the primary control on scapolite composition and may in turn have been controlled by bulk rock composition.  相似文献   

11.
The geochemistry of major and trace elements (including heavy metals and rare earth elements) of the fresh and weathered black shales, and the soils derived from black shales in the Ganziping mine area in western Hunan province (China) were studied using the following techniques: X-ray fluorescence (XRF), inductively coupled plasma mass spectrometer (ICP-MS) and X-ray diffraction (XRD). The results show that the black-shale soils are significantly enriched with Al2O3 and Fe2O3, and depleted of mobile elements CaO, Na2O and K2O. The soils are also highly enriched with heavy metals U, V, Ni, Ba, Cu, Zn and Pb, that may cause potential heavy-metal contamination of the soils. Composition of the soils is homogeneous compared to the weathered black shales, for which the concentrations of major elements except CaO and Na2O, and trace elements except heavy metals (U, V, Ni, Ba, Cu, Zn and Pb) as well as the mobile Sr, show lower variations than in the weathered black shales. Ratios of Zr/Hf, Ta/Nb, Y/Ho, Nd/Sm, and Ti/(Ti + Zr), of the soils are also less variable, with values constantly similar to that of the fresh and weathered black shales correspondingly. Thus, components of the soils are believed to be contributed from the parent black shales through weathering and pedogenesis. It is concluded that the soils were formed by at least two stages of geochemical processes: the early stage of chemical differentiation and the later stage of chemical homogenization. The chemical differentiation that was taken during black-shale weathering might have caused the depletion of CaO and Na2O, and the enrichment of Al2O3 and Fe2O3; while the chemical homogenization that was taken during pedogenesis led to the depletion of SiO2 and K2O, and to the further enrichment of Al2O3 and Fe2O3. The heavy-metal enrichment (contamination) of the soils was then genetically related to the enrichment of Al2O3 and Fe2O3 in the soils.  相似文献   

12.
ABSTRACT

The Boein–Miandasht Complex (BMC) is a part of the Sanandaj–Sirjan metamorphic basement and is cut by gabbroic to granitoid bodies. These intrusive bodies comprise gabbro, gabbro–diorite associated with fine-grained, in part porphyritic leucocratic granitoids. Zircon U–Pb dating of representative gabbro–diorite samples yielded ages of 166.4 ± 1.8 Ma and 163.5 ± 6.3 Ma (Callovian, the latest stage of the Middle Jurassic). Mineral chemistry of the gabbro–diorites shows a homogeneous composition of the main minerals, main augite to diopside clinopyroxene and plagioclase (~An17–59). Moreover, low AlZ/TiO2 ratios of the clinopyroxene grains suggest that the rocks were generated in a within-plate tectonic regime. The SiO2 contents of the gabbro-diorite rocks are between 46.36 and 55.61 wt. %, Al2O3 ranges from 7.57 to 17.98 wt. %. The TiO2 contents vary from 1.18 to 3.65 wt. %, Fe2O3 from 7.41 to 12.95 wt. %, the MgO ranges between 3.49 and 15.75 wt. %, Na2O from 0.65 to 5.08 wt. % and K2O from 0.48 to 1.08 wt. %. These rocks mostly plot in the alkali-gabbro field. Compared to chondrite are characterized by enrichment of LREEs over HREE, enrichment of LIL elements (e.g. Rb, Sr and Ba) and obvious positive anomalies of Nb and Ti. Based on the chemical composition, and mineral composition, this complex was generated in an extensional tectonic regime by partial melting of the hot asthenospheric mantle which is not more consistent with previous models which have suggested for SaSZ evolution in before.  相似文献   

13.
The crystal structure of ludwigite from Vranovac ore deposit (Boranja Mt., Serbia) was refined using the X-ray powder diffraction (XRPD) Rietveld method in the space group Pbam to a final RB=7.45% and RF=5.26%. It has the unit cell dimensions of: a=9.2515(2) ?; b=12.3109(2) ?; c=3.03712(7) ?; and V=345.91(1) ?3. The calculated distances and angles are mostly in good agreement with the Mg2+-Fe2+ substitutions across the M(1) and M(3) sites, as well as with the Fe3+-Al3+ replacement in the M(4) site. However, the mean observed M(2)-O distance is considerably shorter than prescribed, due to a slight increase of the Fe3+ content in the M(2) site. Such replacement was compensated by slight increase of the Fe2+ content in the M(4) site, resulting in the (Mg1.48Fe2+0.46Fe3+0.05Mn0.02)2.01(Fe3+0.94Fe2+0.04Al0.02)1.00B1.00O5 composition. The formation temperature was estimated to be about 500–600°C. The influences of the various chemical compositions to the crystallographic parameters, M-O distances, M(3) and M(4) sites shift, distortion parameters and estimated valences, were also studied and compared with other reference samples.  相似文献   

14.
Saprolites are residual soils which preserve the textures of their parent rocks and thus have evolved by an isovolumetric process of weathering (MILLOT, 1970, The Geology of Clays, Springer). Using bulk density, saprolite elemental analyses can be converted to units of g cm?3. Furthermore, an empirical reaction progress diagram can be constructed for a suite of saprolite samples by plotting element concentrations (in g cm?3) against bulk density (B.D.). Our data for a granite saprolite show that Al2O3 and SiO2 decrease in a linear fashion from B.D. 2.1g cm?3 to 1.5g cm?3 but that K2O follows a curvilinear trend such that it decreases from 75% of its fresh rock value at B.D. 1.6 g cm?3 to nearly zero at B.D. 1.5 g cm?3. The only hypothetical reaction paths that are compatible with these B.D. vs A12O3, SiO2 and K2O constraints are those in which orthoclase alters to kaolinite through an intermediate potassium phase similar to KAl3Si3O10(OH)2 or KAl2Si2O6(OH)3 (hypothetical K-kaolinite). Normative mineral calculations, X-ray diffraction data and structural H2O data are employed to test this conclusion.  相似文献   

15.
Ten dolerite dikes intruded into Triassic fault troughs in the Piedmont area of North Carolina have been analyzed for the contents of major elements plus selected trace elements. The average composition of the initial magma, as indicated by four chill margins for major elements and three for trace elements, is: SiO2, 48.6%; Al2O3, 16.9%; TiO2, 0.57%; Fe2O3, 3.30%; FeO, 6.72%; MgO, 10.59; CaO, 10.42%; Na2O, 2.03%; K2O, 0.20%; MnO, 0.20%; Rb, 2.6 ppm; Sr, 133 ppm; Zr, 46 ppm; Th, 0.4 ppm; and U, below detection limit of approximately 0.1 ppm. One large dike (BP) exhibits a Palisades-type of differentiation by crystal settling of olivine, and the comparatively thick JY dike shows development of micropegmatite toward the center; the smaller dikes, however, are relatively homogeneous across their width. Study of the relationship between SiO2 content and the ratio FeO+Fe2O3/MgO+ FeO+Fe2O3 indicates that most dikes crystallize under conditions of decreasing oxygen pressure, but the differentiation trend of the JY, RD, and RS dikes indicates either constant or increasing oxygen pressure during their evolution.Statistical comparison of the composition of the initial dolerite magmas with a variety of basalt types around the world suggests that the North Carolina dolerites are far more similar to oceanic or oceanic margin tholeiites than to continental tholeiites. The North Carolina rocks are distinctly different from plateau basalts but are similar to the chill zones of the Precambrian Bushveld and Stillwater lopoliths. The comparatively low contents of Th, U, and Sr, plus the relatively high K/Rb ratio all support the possibility that the magmas for the North Carolina dolerites evolved in a dominantly oceanic environment. It seems distinctly possible that continental-type crust and mantle did not exist in the Appalachian Piedmont area in Triassic time, even after major orogeny and the concurrent formation of granitic intrusions.  相似文献   

16.
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   

17.
Melt inclusions in olivine and plagioclase phenocrysts from rocks (magnesian basalt, basaltic andesite, andesite, ignimbrite, and dacite) of various age from the Gorely volcanic center, southern Kamchatka, were studying by means of their homogenization and by analyzing the glasses in 100 melt inclusions on an electron microprobe and 24 inclusions on an ion probe. The SiO2 concentrations of the melts vary within a broad range of 45–74 wt %, as also are the concentrations of other major components. According to their SiO2, Na2O, K2O, TiO2, and P2O5 concentrations, the melts are classified into seven groups. The mafic melts (45–53 wt % SiO2) comprise the following varieties: potassic (on average 4.2 wt % K2O, 1.7 wt % Na2O, 1.0 wt % TiO2, and 0.20 wt % P2O5), sodic (3.2% Na2O, 1.1% K2O, 1.1% TiO2, and 0.40% P2O5), and titaniferous with high P2O5 concentrations (2.2% TiO2, 1.1% P2O5, 3.8% Na2O, and 3.0% K2O). The melts of intermediate composition (53–64% SiO2) also include potassic (5.6% K2O, 3.4% Na2O, 1.0% TiO2, and 0.4% P2O5) and sodic (4.3% Na2O, 2.8% K2O, 1.3% TiO2, and 0.4% P2O5) varieties. The acid melts (64–74% SiO2) are either potassic (4.5% K2O, 3.6% Na2O, 0.7% TiO2, and 0.15% P2O5) or sodic (4.5% Na2O, 3.1% K2O, 0.7% TiO2, and 0.13% P2O5). A distinctive feature of the Gorely volcanic center is the pervasive occurrence of K-rich compositions throughout the whole compositional range (silicity) of the melts. Melt inclusions of various types were sometimes found not only in a single sample but also in the same phenocrysts. The sodic and potassic types of the melts contain different Cl and F concentrations: the sodic melts are richer in Cl, whereas the potassic melts are enriched in F. We are the first to discover potassic melts with very high F concentrations (up to 2.7 wt %, 1.19 wt % on average, 17 analyses) in the Kuriles and Kamchatka. The average F concentration in the sodic melts is 0.16 wt % (37 analyses). The melts are distinguished for their richness in various groups of trace elements: LILE, REE (particularly HREE), and HFSE (except Nb). All of the melts share certain geochemical features. The concentrations of elements systematically increase from the mafic to acid melts (except only for the Sr and Eu concentrations, because of active plagioclase fractionation, and Ti, an element contained in ore minerals). The paper presents a review of literature data on volcanic rocks in the Kurile-Kamchatka area in which melt inclusions with high K2O concentrations (K2O/Na2O > 1) were found. K-rich melts are proved to be extremely widespread in the area and were found on such volcanoes as Avachinskii, Bezymyannyi, Bol’shoi Semyachek, Dikii Greben’, Karymskii, Kekuknaiskii, Kudryavyi, and Shiveluch and in the Valaginskii and Tumrok Ranges.  相似文献   

18.
Melt inclusions were studied in chrome diopside from the Inagli deposit of gemstones in the Inagli massif of alkaline ultrabasic rocks of potassic affinity in the northwestern Aldan shield, Yakutia, Russia. The chrome diopside is highly transparent and has an intense green color. Its Cr2O3 content varies from 0.13 to 0.75 wt %. Primary and primary-secondary polyphase inclusions in chrome diopside are dominated by crystal phases (80–90 vol %) and contain aqueous solution and a gas phase. Using electron microprobe analysis and Raman spectroscopy, the following crystalline phases were identified. Silicate minerals are represented by potassium feldspar, pectolite [NaCa2Si3O8(OH)], and phlogopite. The most abundant minerals in the majority of inclusions are sulfates: glaserite (aphthitalite) [K3Na(SO4)2], glauberite [Na2Ca(SO4)2], aluminum sulfate, anhydrite (CaSO4), gypsum (CaSO4 × 2H2O), barite (BaSO4), bloedite [Na2Mg(SO4)2 × 4H2O], thenardite (NaSO4), polyhalite [K2Ca2Mg(SO4)4 × 2H2O], arcanite (K2SO4), and celestite (SrSO4). In addition, apatite was detected in some inclusions. Chlorides are probably present among small crystalline phases, because some analyses of aggregates of silicate and sulfate minerals showed up to 0.19–10.3 wt % Cl. Hydrogen was identified in the gas phase of polyphase inclusions by Raman spectroscopy. The composition of melt from which the chrome diopside crystallized was calculated on the basis of the investigation of silicate melt inclusions. This melt contains 53.5 wt % SiO2, considerable amounts of CaO (16.3 wt %), K2O (7.9 wt %), Na2O (3.5 wt %), and SO3 (1.4 wt %) and moderate amounts of Al2O3 (7.5 wt %), MgO (5.8 wt %), FeO (1.1 wt %), and H2O (0.75 wt %). The content of Cr2O3 in the melt was 0.13 wt %. Many inclusions were homogenized at 770–850°C, when all of the crystals and the gas phase were dissolved. The material of inclusions heated up to the homogenization temperature became heterogeneous even during very fast quenching (two seconds) producing numerous small crystals. This fact implies that most of the inclusions contained a salt (rather than silicate) melt of sulfate-dominated composition. Such inclusions were formed from salt globules (with a density of about 2.5 g/cm3) occurring as an emulsion in the denser (2.6 g/cm3) silicate melt from which the chrome diopside crystallized.  相似文献   

19.
Generally, P–T pseudosections for reduced compositional systems, such as K2O–FeO–MgO–Al2O3–SiO2–H2O, Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O and MnO–K2O–FeO–MgO–Al2O3–SiO2–H2O, are well suited for inferring detailed P–T paths, comparing mineral assemblages observed in natural rocks with those calculated. Examples are provided by P–T paths inferred for four metapelitic samples from a 1 m2 wide outcrop of the Herbert Mountains in the Shackleton Range, Antarctica. The method works well if the bulk composition used is reconstituted from average mineral modes and mineral compositions (AMC) or when X‐ray fluorescence (XRF) data are corrected for Al2O3 and FeO. A plagioclase correction is suitable for Al2O3. Correction for FeO is dependent on additional microscopic observations, e.g. the kind and amount of opaque minerals. In some cases, all iron can be treated as FeOtot, whereas in others a magnetite or hematite correction yields much better results. Comparison between calculated and observed mineral modes and mineral compositions shows that the AMC bulk composition is best suited to the interpretation of rock textures using P–T pseudosections, whereas corrected XRF data yield good results only when the investigated sample has few opaque minerals. The results indicate that metapelitic rocks from the Herbert Mountains of the Northern Shackleton Range underwent a prograde P–T evolution from about 600 °C/5.5 kbar to 660 °C/7 kbar, followed by nearly adiabatic cooling to about 600 °C at 4.5 kbar.  相似文献   

20.
Coexisting garnets and ilmenites have been synthesized at high pressure (21–40 kb) within the temperature range between 900 and 1100 °C from pyrolite-less-40% olivine and olivine basanite with various water contents. The two compositions yield phases with a range in the 100 Mg/Mg+Fe ratio for both garnet (41–76) and ilmenite (15–47). The distribution coefficient for iron and magnesiaum (K D(Fe, Mg) ilm-ga = 4.0±0.5) for coexisting phases does not appear to vary with change in the bulk composition or temperature of synthesis. The synthesized ilmenites are of similar composition to those of kimberlites in 100 Mg/Mg+Fe ratio and Al2O3 and Cr2O3 solid solution. Cr2O3 content in ilmenite is dependent on Cr2O3 in the bulk composition and also on Fe2O3 content of ilmenite. Fe2O3 content of ilmenite is very sensitive to f O2 and natural ilmenites from peridotites have formed under low f O2. Al2O3 solid solution in ilmenite as well as TiO2 in coexisting garnet tend to be higher with higher temperature. All the variety of compositions of ilmenites from kimberlites may be obtained from rocks rather close in composition to those used in experiments, within the same range of pressure and temperature but at variable oxygen fugacities.  相似文献   

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