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1.
Summary The mineral chemistry of a Variscan lamprophyre (kersantite) from the Frankenwald, Germany, has been investigated by electron microprobe. This potassic, Si-saturated, mafic rock contains an assemblage of different generations of titanite and allanite-(Ce), Th-rich zircon, and metamict REE–Ti–Zr–Th silicates. The primary ferroan-ceroan titanite contains unusually high contents of REE2O3 (max. (ΣLa to Sm)+Y = 36.8 oxide wt.%), ZrO2 (max. 5.4 wt.%), and ThO2 (max. 3.1 wt.%). Its empirical formula averages to (Ca0.31 La0.17 Ce0.30 Pr0.03 Nd0.08 Sm0.01 Y0.01 Fe2+0.06 Th0.02 Mn0.01)Σ1.00 (Ti0.60 Fe2+0.22 Al0.06 Zr0.07 Mg0.04 Nb0.01)Σ1.00 O1.00(Si0.93 Al0.07)Σ1.00 O4. Element correlations reveal operation of the complex substitution Ca2++Ti4++Th4+ ⇔ REE3++Al3++Zr4+. In comparison to allanite-(Ce), ferroan-ceroan titanite preferentially incorporated the LREE and Th. This finding is inconsistent with previous experimental studies and suggests that both minerals are not cogenetic. High Zr contents in titanite, usually known only from Si-undersaturated alkaline rocks, and the predominance of Fe2+ suggest that the ferroan-ceroan titanite crystallized from an alkali-rich, low-fO2 residual melt.  相似文献   

2.
Al- and F-rich titanite (3.862O3 <9.33 wt%, 0.931(F, OH)1Ti-1O-1 substitution within single crystals, particularly at grain boundaries with omphacite and/or phengite. In-situ ion microprobe U-Pb analysis of titanite domains that have various Al and F contents yielded apparent 206Pb/238U ages scattering between 283 and 153 Ma. Chemical and petrological data are indispensable to interpret this complex age distribution, and the good correlation between 206Pb/238U ratios and Al content indicates that the Al- and F-rich titanite was formed during pre-Alpine metamorphism (𔕑ᆟ Ma). Progressively younger ages are obtained in domains with decreasing Al and F content, suggesting that partial chemical re-equilibration was responsible for the incomplete isotopic resetting during Alpine metamorphism. Petrological and U-Pb data show that Al- and F-rich titanite should be used with caution to infer high-pressure conditions in polymetamorphic carbonate systems.  相似文献   

3.
In metabasites from the high‐grade metamorphic Kimi Complex of the Greek Rhodope, lamellae of quartz and amphibole were observed together with either rutile or titanite precipitates in the cores of clinopyroxene that underwent a prolonged exhumation history from eclogite via granulite and amphibolite facies conditions. Lamellae are crystallographically oriented along clinopyroxene cleavage planes (010) and interpreted as the result of precipitation during a two‐step intracrystalline compositional adjustment from an omphacite‐ to a Ca‐Tschermak‐rich clinopyroxene and finally to diopside. Even though retrograde diffusion profiles develop in clinopyroxene, the diffusion rates of highly charged ions like Si4+, Al3+and Ti4+are too slow, so precipitates rich in Si4+ (quartz), Al3+(amphibole) and Ti4+(rutile or titanite) form as viable kinetic alternatives. These precipitation reactions are not possible isochemically, and additional exchange of ions with the matrix is required for precipitation to occur. This exchange of mainly rapidly diffusing low‐charge ions is postulated to proceed by bulk diffusion (self‐diffusion) and does not require special pathways or fluid, even though these may play an additional role during metamorphism. This hitherto undescribed process of precipitation made possible by diffusional exchange with the matrix through an intact host crystal lattice is termed here as ‘open system precipitation’ (OSP). No prior Ca‐Eskola‐rich (ultrahigh‐pressure, UHP) composition of omphacite is required to explain the observed precipitates. It is proposed that many precipitation phenomena that were hard to explain in a closed‐system scenario can now be explained more readily by OSP. Calculation of an original solid solution composition, as in an UHP phase, from precipitate and host mineral analyses becomes imprecise to the degree that bulk diffusion and hence OSP have been important.  相似文献   

4.
The intermetallic compound Ni3Au and Au-Ni solid solutions (native nickel Au and Au-bearing native Ni) were found in the contact metamorphosed metalliferous sediments of the Triassic chert formation in Sikhote-Alin. The metalliferous rocks are characterized by high contents of Au, Ag, and PGE, as well as the presence of diverse minerals of precious metals. Nickel gold (Au0.91-0.88 Ni0.09-0.12) is found as grains and crystals (3 to 4 im in size) in Au-bearing cherts with hematite, which are conventionally defined as “itabir-ites” and in the altered siliceous rocks of the Dal’nerechensky district (the upper reaches of the Gornya River). The nickel gold is associated with copper Au, pure native Au (Au1.00), and Au-Ag and Au-Ag-Pb solid solutions (Au0.86/0.84Ag0.14_0.16 and Au0.78Ag0.19Pb0.03, respectively). The Au-bearing Ni is found in the metamorphosed carbonaceous mudstones and Au-bearing “itabirites” of the Shirokopadninsky area (Olgin-sky district). The Au content varies from 6.09 wt % (Ni0.98Au0.02) to 11.30 wt % (Ni0.96Au0.04) in some Au-bearing Ni grains (about 10—15 im in diameter) taken from the metamorphosed mudstones. The grains of Au-bearing Ni (Co0.001_0.00Au00.2 - 0.17 Ni 0.98_0.83) in the “itabirites” are also characterized by their heterogeneous composition and the fine impregnation of the Ni3 Au intermetallic compound (Ni2.99Au1.01 based on the microprobe analysis).  相似文献   

5.
The particularity of the formation of the skarn lodes of the Cretaceous-Paleogene Belogorsk deposit is the intense replacement of the early mineral assemblages (the decomposition of garnet, pyroxene, and pyroxenoids) with decreasing temperature, the increase in the amount of magnetite at the expense of Fe released from the decomposed minerals, and the formation of quartz and volatile-rich compounds (calcite, fluorite, amphibole, and sulfides). The geochemical and mineralogical similarity suggests a genetic relation between the manganese skarn lodes of the Belogorsk deposit (the Ol’ginsk ore district) and the stratabound bodies of the manganese silicate rocks (the Triassic contact metamorphosed metalliferous sediments) of the adjacent Shirokaya Pad area (as a source of matter).  相似文献   

6.
Lamellar intergrowths of actinolite and hornblende or aluminous actinolite occur in metamorphosed igneous rocks in the Hitachi metamorphic district, southern Abukuma Plateau. Electron microprobe analyses of five pairs are presented. The Fe-Mg partitioning and the miscibility gap are discussed in terms of an Mg-Fe-AlIV diagram. The Fe-Mg partition coefficients depend on the AlIV contents in hornblendes in a manner indicating that the pairs are close to equilibrium. Calcic amphibole pairs of high Fe/Mg ratio are richer in AlIV than those with low ratio. The AlIV content of the coexisting actinolite first increases with rising temperature, but then decreases as the temperature increases further. On the other hand, the AlIV content of coexisting hornblende-aluminous actinolite successively decreases with rising temperature.  相似文献   

7.
Synthetic titanite, CaTiOSiO4, and the series of (Ca1−x Na x )(Ti1−x Ta x )OSiO4 and Ca(Ti1−2x Ta x Al x )OSiO4 solid solutions have been prepared by ceramic methods, and their crystal structure determined by the Rietveld analysis. At ambient conditions, titanite can contain up to 20 mol% NaTaOSiO4 or 60 mol% Ca(Al0.5Ta0.5)OSiO4. These limits might differ in natural samples due to combination with substitutions involving fluorine and/or hydroxyl replacing oxygen together with vacancies at cationic sites. All cations located at the vii X- and vi Y-sites in the structures of tantalian titanite are disordered. Expansion of the <Si–O> bond from 1.618 to 1.621 Å in CaTi0.8Ta0.1Al0.1OSiO4 and CaTi0.6Ta0.2Al0.2OSiO4 to 1.644 Å in the CaTi0.4Ta0.3Al0.3OSiO4 titanite suggests the possible presence of some Al3+ in the tetrahedral site replacing Si4+ in the latter. All tantalian titanites crystallize in the space group A2/a. This implies that both single-site and complex double-site substitutional schemes induce P21/a → A2/a phase transition(s). The (Ca1−x Na x )(Ti1−x Ta x )OSiO4 substitution scheme incorporates larger cations at both the vii X and vi Y sites, whereas the Ca(Ti1−2x Ta x Al x )OSiO4 scheme involves only vi Y-site (Al3+,Ta5+) cations with a slightly smaller “average” radius. Unit cell dimensions change insignificantly or increase incrementally with increase of average cationic radii in the (Ca1−x Na x )(Ti1−x Ta x )OSiO4 series, and with an insignificant decrease in the viR Y average cationic radii in the Ca(Ti1−2x Ta x Al x )OSiO4 series. Both Ta-doped titanite and CaTiOSiO4 consist of distorted polyhedra with the XO7, YO6 coordination polyhedra and the SiO4 tetrahedron in tantalian titanite being less distorted compared to those of the pure CaTiOSiO4.  相似文献   

8.
Over thirty samples of natural Ti-bearing amphiboles with Ti- and Fe-contents ranging from 0.111 to 0.729 atom per formula unit (a.p.f.u.) and from 0.479 to 2.045 a.p.f.u., respectively, were studied by means of optical absorption spectroscopy and microprobe analysis. Thirteen samples were also studied by Mössbauer spectroscopy. A strong pleochroic absorption edge, causing the dark brown colours of Ti-bearing amphiboles, is attributed to ligand-metal and metal-metal charge transfer transitions involving both iron and titanium ions (O2?→ Fe3+, Fe2+, O2?→ Ti4+ and Fe2+ + Ti4+→ Fe3+ + Ti3+). A broad intense Y-polarized band ～22?000?cm?1 (ν1/2?≈?3700?cm?1) in spectra of two low iron amphiboles with a relatively low Fe3+/Fetotal ratio, both from eclogite-like rocks in kimberlite xenoliths, was attributed to electronic Fe2+(M3) + Ti4+(M2)→Fe3+(M3)+Ti3+(M2) IVCT transitions. The IVCT bands of other possible ion pairs, involving Ti4+ and Fe2+ in M2 and M1, M4 sites, respectively, are presumed to be at higher energies, being obscured by the absorption edge.  相似文献   

9.
Some of the most vanadium-rich silicate minerals known are present in green mica schist from the Hemlo gold deposit, Ontario, Canada. Vanadium-rich silicate minerals include green mica (up to 17.6 wt. % V2O3), phlogopite (10.1 wt. % V2O3), pumpellyite (25.7 wt. % V2O3), garnet (18.5 wt. % V2O3), epidote-group minerals (9.1 wt. % V2O3), antimonian vesuvianite (4.3 wt. % V2O3), and titanite (18.5 wt. % V2O5). In addition, minor amounts of V (<2 wt. % V2O3) are present in tourmaline, chlorite, talc and tremolite in other lithologies of the Hemlo deposit. The principal substitution that incorporates V into most of these silicate minerals is Al3+=V3+ in octahedral positions. Vanadium is incorporated into phlogopite mainly by the two substitutions: 3Mg2+ =2V3++ and VIMg2++IVSi4+=VIV3+ +IVAl3+, and all of the three substitutions Ti4++O2- =V3++(OH,F)-, Ti4+=V4+, and 5Ti4+=4V5+ + may have operated in titanite.Vanadium-enriched green mica schist from the Hemlo gold deposit is characterized by uniform Ti/Zr ratios, systematically low Ti, Ni, Co and Sc abundances, and low levels of incompatible elements Th, U, Hf and Zr and is distinct in these respects from its Cr-enriched counterpart. These geochemical features, along with textural evidence (relict quartz and oligoclase phenocrysts), indicate that the V-enriched green mica schist from Hemlo was most likely derived mainly from quartz-oligoclase porphyry. However, its anomalously high V and Cr contents were probably introduced metasomatically from local maficultramafic sources and were fixed in green mica and oxides during the waning of a second regional metamorphism. Vanadium was further remobilized, and its concentration probably enhanced, during the late hydrothermal alteration, which resulted in the formation of the characteristic V-rich calc-silicate minerals.  相似文献   

10.
A new heterophyllosilicate mineral schüllerite was found in the L?hley basalt quarry in the Eifel volcanic region, Germany, as a member of the late mineral assemblage comprising nepheline, leucite, augite, phlogopite, magnetite, titanite, fresnoite, barytolamprophyllite, fluorapatite, perovskite, and pyrochlore. Flattened brown crystals of schüllerite up to 0.5 × 1 × 2 mm in size and their aggregates occur in miarolic cavities of alkali basalt. The mineral is brittle, with a Mohs hardness 3–4 and perfect cleavage parallel to (001). D calc = 3.974 g/cm3. Its IR spectrum is individual and does not contain bands of OH−, CO32− or H2O. Schüllerite is biaxial (−), α = 1.756(3), β = 1.773(4), γ = 1.780(4), 2V meas = 40(20)°. Dispersion is weak, r < ν. Pleochroism is medium X > Y > Z, brown to dark brown. Chemical composition (electron microprobe, mean of five-point analyses, Fe2+/Fe3+ ratio determined by the X-ray emission spectroscopic data, wt %): 3.55 Na2O, 0.55 K2O, 3.89 MgO, 2.62 CaO, 1.99 ArO, 28.09 BaO, 3.43 FeO, 8.89 Fe2O3, 1.33 Al2O3, 11.17 TiO2, 2.45 Nb2O5, 26.12 SiO2, 2.12 F, −0.89 -O=F2, 98.98 in total. The empirical formula is (Ba1.68Sr0.18K0.11Na1.05Ca0.43Mn0.47Mg0.88Fe0.442+Fe1.023+Ti1.28Nb0.17Al0.24)Σ7.95Si3.98O16.98F1.02. The crystal structure was refined on a single crystal. Schüllerite is triclinic, space group P1, unit cell parameters: a = 5.4027(1), b = 7.066(4), c = 10.2178(1)?, α = 99.816(1), β = 99.624(1), γ = 90.084(1)°, V = 378.75(2) ?3, Z = 1. The strongest lines of the X-ray powder diffraction pattern [d, ?, (I, %)]: 9.96(29), 3.308(45), 3.203(29), 2.867(29), 2.791(100), 2.664(46), 2.609(36), 2.144(52). The mineral was named in honor of Willi Schüller (born 1953), an enthusiastic, prominent amateur mineral collector, and a specialist in the mineralogy of Eifel. Type specimens have been deposited at the Fersman Mineralogical Museum of the Russian Academy of Sciences, Moscow, registration no. 3995/1,2.  相似文献   

11.
Simon et al. (2005) reported low Ti3+/Ti4+ values in Ti-rich pyroxenes in the Wark-Lovering rim (WL) of a Leoville CAI (144A) as compared to the interior of the inclusion. These electron microprobe analyses were interpreted as evidence that the growth of the WL rim is the manifestation of an evolution to a more oxidizing environment. Further work by Simon et al. (2007) used XANES analyses to argue for higher Ti3+ abundances and interpreted the data of Simon et al. (2005) as the result of X-ray contamination by neighboring phases, specifically spinel. Late-stage alteration was also included as a possible explanation.To investigate further the oxidation state of Ti in WL rims, we re-analyzed Leoville 144A to obtain a more complete data set of Ti3+/Ti4+ values in the Wark-Lovering rims. We conducted experiments on spinel-mixing to determine whether this was a plausible explanation for the observed paucity of Ti3+ in WL rims. While we found a wider range of Ti3+/Ti4+ in these WL rim data than in our original study, our new data show that the original conclusion that rims are lower in Ti3+/Ti4+ than interiors remains valid. We conclusively rule out spinel-mixing as an explanation for our data, and we see no clear inconsistency between our electron microprobe data and the XANES data. The WL rim of CAI Ef3 was also analyzed by EMPA and compared to the results of Leoville 144A.To predict compositional consequences of this hypothesis, we constructed a reaction space between Ti-rich pyroxene in the WL rim, perovskite, Mg(g), Ca(g), O2(g), and SiO(g). We find the oxidation of Ti3+, coupled with Ti loss via perovskite formation, explains many features of WL rim EMPA analyses. We maintain that the WL rim pyroxenes are compositionally distinct from those in the interior, and are evidence of a more oxidizing environment during WL rim formation.  相似文献   

12.
Summary Chemical compositions of orthopyroxene and clinopyroxene from the Jinchuan ultramafic intrusion have been obtained by electron microprobe analysis. The Mg number (MgO/(MgO + FeO)) for both pyroxenes falls within narrow ranges, 82–87 for clinopyroxene and 81–85.5 for orthopyroxene, suggesting limited magma differentiation in regard to the present igneous body. The Al2O3 content ranges from 2.44 wt.% to 4.43 wt.% and increases with decreasing Mg of the pyroxenes, i.e., with the more evolved magma. This is attributed to the relatively greater effects of Al2O3, TiO2, Cr2O3 and Fe2O3 than that of SiO2 on pyroxene crystallization.Negative linear relationships between Ti4+ and Si4+, and Al3+ and Si4+ characterize the pyroxenes. In clinopyroxene, regression of Si4+ versus Al3+ results in a straight line with a slope of –1.012, indicating that the decrease of Si4+ in the crystal structure is matched by an increase only in tetrahedral Al3+; octahedral Al3+ has remained relatively constant. The negative linear relationship between Ti4+ and Si4+ in clinopyroxene reflects either a greater tendency of Ti4+ to occupy octahedral sites than Al3+, or that replacement of Al3+ for Si4+ demands a more efficient charge balance. The scatter in plots of Ti4+ versus Si4+ for orthopyroxene indicates that charge balance is not as critical as structure symmetry.The crystallization temperature of pyroxene is calculated to be 1108–1229°C usingWood andBanno's (1973) two pyroxene thermometer, and is within 40°C of that calculated fromWells's (1977) thermometer. The distribution coefficient (Kd) for Mg2+ and Fe2+ between clinopyroxene and orthopyroxene is estimated to be 0.86, which is higher than that of the other intrusions and lower than that of mantle nodules, but still falls within their Kd-1/T trend. This suggests that the Kd value of pyroxene is controlled mainly by temperature.
Mineralchemie der Pyroxene der Jinchuan-Intrusion, China
Zusammenfassung Die chemische Zusammensetzung von Orthopyroxenen und Klinopyroxenen aus der ultramafischen Jinchuan Intrusion wurden mit der Mikrosonde bestimmt. Die Mg-Zahl (MgO/(MgO + FeO)) beider Pyroxene liegt innerhalb enger Grenzen, 82–87 für Klinopyroxen und 81–85.5 für Orthopyroxen. Dies weist auf beschränkte magmatische Differentiation der Intrusion hin. Der Al2O3-Gehalt liegt zwischen 2.44 Gew.%. und 4.43 Gew.%. und nimmt mit der abnehmenden Mg-Zahl der Pyroxene ab, d.h. mit dem mehr entwickelten Magma. Dies wird damit erklärt, daß Al2O3, TiO2, Cr2O3 und Fe2O3 einen größeren Einfluß auf die Kristallisation der Pyroxene ausüben als SiO2.Die Pyroxene werden durch negative lineare Beziehungen zwischen Ti4+ und Si4+, sowie Al3+ und Si4+ charakterisiert. In Klinopyroxenen resultiert die Regression von Si4+ gegen Al3+ in einer geraden Linie mit einer Neigung von –1.012. Dies weist darauf hin, daß die Abnahme der Si4+ Gehalte in die Kristallstruktur durch Zunahme von ausschliesslich tetraedrischem Al3+ kompensiert wird; oktaedrisches Al3+ ist relativ konstant geblieben. Die negative lineare Beziehung zwischen Ti4+ und Si4+ in Klinopyroxenen geht entweder auf eine stärkere Tendenz des Ti4O2, oktaedrische Plätze zu besetzen zurück, oder darauf daß ein Ersatz von Al3+ für Si4+ einen effizienteren Ladungsausgleich verlangt. Die unregelmäßige Verteilung der Plots von Ti4+ gegen Si4+ in Orthopyroxenen läßt erkennen, daß Ladungsausgleich hier nicht so kritisch ist wie die Symmetrie der Struktur.Die Kristallisationstemperatur der Pyroxene wurde mit dem Zwei Pyroxenthermometer nachWood undBanno (1973) mit 1108–1229°C bestimmt. Diese Werte liegen innerhalb von 40°C des vonWells (1977) berechneten. Der Verteilungskoeffizient (Kd) für Mg2+ und Fe2+ zwischen Klinopyroxen und Orthopyroxen wird auf 0.86 berechnet; das ist höher als der aus anderen Intrusionen und niedriger als der von Mantelxenolithen, fällt aber immer noch innerhalb des Kd-1/T Trends derselben. Dies legt den Gedanken nahe, daß der Kd Wert der Pyroxene hauptsächlich durch Temperatur bestimmt wird.

With 6 Figures  相似文献   

13.
A crystal chemical investigation of clinopyroxenes from a suite of nepheline-bearing lavas located in the Nyambeni Range of Kenya has delineated the polyhedral site configurations and related intracrystalline relationships. These are distinct from those determined for the clinopyroxene in an analogous suite of leucite-bearing lavas from the Sabatini volcanoes in the Roman Region of Italy (Dal Negro et al. 1985).The Nyambeni clinopyroxene, varying from salite to hedenbergite, preferentially accepts Na in the M2 site to balance increasing Fe2+ and Si, respectively, whereas the Sabatini clinopyroxene is confined within the salite field and preferentially accepts Aliv to balance the effect of increasing (Fe3++Ti4++Alvi+Cr3+)M1.The Fe2+/Fe3+ and K/Na ratios of the host rocks emerge as significant factors in determining the different polyhedral configurations and evolutions of the clinopyroxene from the two lava suites, respectively. The resulting Mg-Fe2+ order-disorder relationships in M1–M2 are also distinct in the two clinopyroxenes. A high degree of MgFe2+ order in M1–M2 corresponds to the largest configurational, hence energetic, difference between M1 and M2 in the Nyambeni clinopyroxene, whereas the converse applies to the Sabatini clinopyroxene.In view of the significant crystal chemical differences and distinct evolution trends, it is proposed that salites from alkali volcanic rocks may be referred to as Nyambeni-type or Sabatini-type, respectively.  相似文献   

14.
Summary The highest (Nb, Ta) content ever encountered in titanite is reported from the Maríkov 11 pegmatite in northern Moravia, Czech Republic. This dike is a member of a pegmatite swarm of the beryl-columbite subtype, metamorphosed under conditions of the amphibolite facies. The pegmatite carries, i.a., rare tantalian rutile intergrown with titanian ixiolite, titanian columbite-tantalite, fersmite and microlite. Fissures generated in the Nb, Ta oxide minerals during deformation are filled with titanite, formed by reaction of the oxide minerals with metamorphic pore fluids. The titanite displays limited degrees of substitutions Na(Ta > Nb)(CaTi)–1, (Ta > Nb)4Ti–4Si–1 and AI(OH, F)(TiO)–1, but an extensive (and occasionally the sole significant) substitution (Al > Fe3+)(Ta > Nb)Ti–2, responsible for widespread oscillatory zoning. This substitution reduces the proportion of the titanite componentsensu stricto, CaTiSiO4,O, to less than 50 mole % in many analyzed spots. The extreme composition corresponds to (Ca0.994Na0.011)(Ti0.436Sn0.007Al0.280Fe3+ 0.006Ta0.199Nb0.079)Si0.988O4(O0.974F0.026). However, so far this substitution fails to generate compositions that would define a new species.
Zusammenfassung Die AI(Nb, Ta)Ti–2 Substitution im Titanit: Auftauchen einer neuen Mineralspecies? Die höchsten (Nb, Ta) Gehalte, die jemals für Titanit gefunden wurden, werden für den Maríkov II Pegmatit in Nordmähren, Tschechei, berichtet. Der Intrusivgang ist Teil eines Amphibolit-faziell überprägten Pegmatitschwarms vom Beryll-Columbit Subtypus Der Pegmatit führt u.a. seltene tantalbetonte Rutile verwachsen mit titanbetontem Ixiolith, titanbetontem Columbit-Tantalit, Fersmit and Mikrolith. Deformationsbedingte Frakturen in den (Nb, Ta) Oxiden sind mit Titanit, als Folge der Reaktion der metamorphen Porenlösungen mit den Oxidmineralen, verkittet. Titanit zeigt begrenzte Substitutionen Na(Ta > Nb)(CaTi)–1,(Ta > Nb)4Ti–4Si–1 and Al(OH, F)(TiO)–1, aber extensive (und gelegentlich einzig bedeutsame) Substitution (Al >> Fe3+)(Ta > Nb)Ti–2, die eine weitverbreitete, oszillierende Zonierung hervorruft. Diese Substitution verringert den Anteil der Titanit-Komponentesensu stricto, CaTiSiO,O, auf weniger als 50 Mol% in vielen Analysen. Die Extremzusammensetzung entspricht Ca0.994Na0.11) (T10.436Sn0.007Al0.280Fe3+ 0.006Ta0.199Nb0.079)Si0.988O4(O0.974F0.026). Das AusmaB dieser Substitution ist unzureichend, um eine neue Mineralspecies zu definieren.
  相似文献   

15.
Kyzylkumite has been found in Cr-V-bearing metamorphic rocks of the Sludyanka Complex, Southern Baikal region; it has been identified by X-ray powder diffraction method. This is a late secondary mineral developed after Ti-V-oxides (schreyerite, berdesinskiite) and V-bearing rutile and titanite. Kyzylkumite represents a new structural type with composition Ti4V 2 3+ O10(OH)2 corresponding to octahedral coordination of Ti4+ and V3+. Its unit-cell dimensions are: a = 8.4787(1), b = 4.5624(1), c = 10.0330(1) Å, β = 93.174(1)°. The ideal formula of kyzylkumite Ti4V 2 3+ O10(OH)2 corresponds to composition, wt %: 65.56 TiO2, 30.75 V2O3, 3.69 H2O. Indeed, the contents (wt %) of these constituents range from 62 to 70 TiO2 and from 23 to 33 V2O3. Variations in contents and the Ti/V value are caused by partial substitution V3+ for V4+, isovalent substitutions Ti4+ and V3+ for V4+ and Cr3+, respectively, and coupled substitution V3+ + OH? ? Ti4+ + O2?. Smyslova et al. (1981)—the discovereres of kyzylkumite—assumed its composition to be the same as for schreyerite V 2 3+ Ti3O9 that principally different from kyzylkumite from the Sludyanka Complex. Therefore, re-examination of the kyzylkumite holotype or cotype from its type locality is needed.  相似文献   

16.
Activities of titanite (Ttn, CaTiSiO5) and/or rutile (Rt, TiO2) phase components were calculated for 45 well‐characterized natural titanite‐ or rutile‐undersaturated epidote–amphibolites by using the equilibria: (i) 3 anorthite + 2 zoisite/clinozoisite + rutile + quartz = 3 anorthite + titanite + water (referred to as TZARS) and (ii) anorthite + 2 titanite = grossular + 2 rutile + quartz (referred to as GRATiS). In titanite‐bearing and rutile‐absent samples aRt is 0.75 ± 0.26. In titanite‐absent, rutile‐bearing samples aTtn is 0.89 ± 0.16. Mean values derived for aRt/aTtn are 0.92 ± 0.12 for rutile + titanite‐bearing samples and 0.42 ± 0.27 for samples lacking both titanite and rutile. Use of these values with TZARS yields pressure estimates for epidote–amphibolites that differ on average by <0.5 kbar from those recorded by established mineral barometers, even where both titanite and rutile are lacking. Despite rather large uncertainties in the average values obtained for aRt, aTtn or aRt/aTtn, application of TZARS yields pressure estimates that agree with independent estimates to within ±0.5 kbar for titanite‐ and/or rutile‐saturated samples, and to within ±0.8 kbar for samples that contain neither Ti‐phase. The accuracy and precision of the TZARS barometer are comparable to that of many well‐calibrated barometers. TZARS offers a much‐needed barometer for mafic rocks metamorphosed at epidote‐bearing amphibolite and blueschist facies conditions. In addition, the results provide a basis for application of other thermobarometers, such as Ti‐in‐zircon, where rutile activity is required as input.  相似文献   

17.
徐跃通 《地质科学》1998,33(1):39-50
在信江盆地中存在数层和石炭纪海相火山岩及其海底块状硫化物矿层相伴生,与石炭纪地层整合产出的层状硅质岩。由对硅质岩常量元素、微量元素、稀土元素、硅和氧同位素等地球化学特征研究表明,本区硅质岩具有一定的热水沉积硅质岩地球化学特征。在Al-Fe-Mn和Fe-Mn-(Ni+Co+Cu)三角图上,本区硅质岩属热水沉积硅质岩。由硅质岩MnO/TiO2比值、δCe值和δ30Si值分析表明,信江盆地石炭纪硅质岩的沉积环境主要为浅海。  相似文献   

18.
首次在班公湖-怒江缝合带西段去申拉组中发现了泥质硅质岩,呈2个层位产出。为探讨泥质硅质岩的沉积环境、成因及与班-怒特提斯洋西段构造演化的关系,进行岩石学和地球化学分析,结果显示,第一层位泥质硅质岩Al_2O_3/(Al_2O_3+Fe_2O_3)、Ce/Ce~?、(La/Ce)_N、V/(Ni+V)、Ce/La、Ce_(anom)、Eu_(anom)平均值分别为0.60、0.80、1.24、0.72、1.84、-0.08、0.01,第二层位泥质硅质岩相应比值平均值分别为0.65、0.83、1.16、0.77、1.97、-0.07、0.02。结合泥质硅质岩的Fe_2O_3/TiO2-Al_2O_3/(Al_2O_3+Fe_2O_3)、(La/Ce)N-Al_2O_3/(Al_2O_3+Fe_2O_3)、Hf/3-Th-Ta关系图解,表明第一、二层位泥质硅质岩形成于活动大陆边缘,沉积时水-岩界面为水体分层不强烈的厌氧环境。U-Th、Zn-Ni-Co、La-Ce、La/Yb-REE关系图解和稀土元素特征指示了第一、二层位泥质硅质岩为热水成因,热水活动与玄武岩岩浆活动有关,第二层位泥质硅质岩沉积时热水活动更强烈。去申拉组泥质硅质岩的岩石学、地球化学特征表明,狮泉河地区班-怒特提斯洋至少在早白垩世仍具有一定规模的洋盆,其闭合时间应晚于约109Ma,进一步限定了洋盆的闭合时间。  相似文献   

19.
内蒙古阿拉善地区经历数亿年的地质活动,产出颜色丰富且结构致密的戈壁玛瑙。通过常规宝石学测试、偏光显微镜及扫描电镜观察、X射线粉晶衍射、电子探针、红外光谱及紫外-可见光-近红外分光光度计等测试分析方法对绿色戈壁玛瑙的宝石矿物学特征及致色成因进行了深入研究。肉眼观察,阿拉善绿色玛瑙呈深绿色至褐绿色,微透明至不透明,相对密度、折射率、摩氏硬度等均符合石英质玉石的特点。偏光显微镜观察,绿鳞石富集于表层,并向内部呈放射状生长;方解石与石英均为隐晶质结构。扫描电镜观察,绿鳞石呈颗粒状分布于石英及方解石之间。X射线衍射分析结果表明,绿色戈壁玛瑙的物相组成主要为石英、方解石和绿鳞石。电子探针分析结果表明绿鳞石的主要化学组成为SiO2、FeO、Al2O3、K2O和MgO。红外光谱分析也显示存在绿鳞石对应基团的特征峰。表层绿鳞石在紫外-可见光-近红外分光光度计下显示出Fe2+与Fe3+的特征光谱,Fe2+与Fe3+之间的电荷转移是其...  相似文献   

20.
In the metamorphosed manganese oxide ores of India, braunite is ubiquitous in all assemblages from chlorite to sillimanite grades. Chemical analyses of braunite from different prograde assemblages confirm the presence of a fixed R2+ (=Mn2++Mg+Ca) SiO3 molecule in the mineral. Element partitioning between coexisting braunite and bixbyite indicates a near-ideal mixing of Fe+3/ -Mn+3 in the phases. This also indicates that braunite became relatively ferrian while equilibrating with associated phases such as bixbyite, hollandite and jacobsite during prograde reactions. Petrogenetic studies show that as a general trend, prograde lower oxide phases appeared by deoxidation of higher oxide phases. But braunite, a more reduced phase than bixbyite, appeared early from deoxidation of pyrolusite in presence of quartz. Bixbyite could appear later from the reacting pyrolusite-braunite-quartz assemblage. Inferred mineral reaction paths and the general trend of pro-grade deoxidation reactions suggest that the composition of ambient fluid phase was internally buffered during metamorphism.  相似文献   

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