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1.
Single-crystal Raman spectra of synthetic end-member uvarovite (Ca3Cr2Si3O12) and of a binary solution (59% uvarovite, 41% andradite) have been measured using single crystal techniques. For each of these garnets, 22 and 21 of the 25 Raman modes were located, respectively. The spectra for uvarovite garnets closely resemble those of the other calcic garnets, grossular, and andradite. The modes for uvarovites do not fit into the same trends as established by the other five anhydrous end-member garnets: the high energy “internal” Si–O modes do not depend on lattice constant in uvarovite. They exceed frequencies for both andradite and grossular. This is likely due to the large crystal field stabilization energy of trivalent chromium. The low energy and midrange modes are at similar frequencies to the other calcic garnets.  相似文献   

2.
This work considers the studies of melt and fluid inclusions in spinel of ultramafic rocks in the mantle wedge beneath Avacha volcano (Kamchatka). The generations of spinel were identified: 1 is spinel (Sp-I) of the “primary” peridotites, has the highest magnesium number (#0.69–0.71), highest contents of Al2O3 and lowest contents of Cr2O3 (26.2–27.1 and 37.5–38.5 wt %, respectively), and the absence in it of any fluid and melt inclusions; 2 is spinel (Sp-II) of the recrystallized peridotites, has lower magnesium number (Mg# 0.64–0.61) and the content of Al2O3 (18–19 wt %), a higher content of Cr2O3 (45.4–47.2 wt %) and the presence of primary fluid inclusions; 3 is spinel (Sp-III) that is characterized by the highest content of Cr2O3 (50.2–55.4 wt %), the lowest content of Al2O3 (13.6–16.6 wt %), and the presence of various types of primary melt inclusions. The data obtained indicate that metasomatic processing of “primary” peridotites occurred under the influence of high concentrated fluids of mainly carbonate-water-chloride composition with influx of the following petrogenic elements: Si, Al, Fe, Ca, Na, K, S, F, etc. This process was often accompanied by a local melting of the metasomatized substrate at a temperature above 1050°C with the formation of melts close to andesitic.  相似文献   

3.
Summary Fe-Ti-P-rich rocks (FTP) are unusual with respect to their mineralogy and bulk composition. Varieties of these rocks are mostly related to Proterozoic massif-type anorthosites and to a lesser extent to the upper parts of mafic-ultramafic intracratonic layered complexes and other igneous rock suites. We present results on the geology, mineralogy and geochemistry of a new occurrence of FTP, associated with mafic rocks in the northwestern part of Iran. The Qareaghaj mafic-ultramafic intrusion (QMUI) is a small igneous body situated between Palaeozoic sedimentary rocks and a Precambrian low grade metamorphic complex. The QMUI is composed mainly of non-mineralized mafic and apatite- and Fe-Ti oxide-rich ultramafic rocks. The mafic rocks, mainly coarse-grained gabbro, microgabbro and amphibolite, have a simple mineral assemblage (plagioclase + clinopyroxene + ilmenite) and based on field observations, mineralogy and chemical composition are comagmatic. The ultramafic rocks with high proportion of olivine (∼40–66 vol.%), apatite (∼0.1–16 vol.%), ilmenite (∼11–19 vol.%) and magnetite (∼2–13 vol.%), have unusual bulk compositions (e.g., SiO2 ∼ 21–30 wt.%, total iron expressed as Fe2O3 tot ∼ 26–42 wt.%, TiO2 ∼ 5–11 wt.%, MgO ∼ 9–20 wt.%, P2O5 up to 5.1 wt.%, Cr ∼ 40–160 ppm, Ni ∼ 7–73 ppm). The FTP forms numerous sill-like layers, ranging in thickness from ∼5 cm to few meters. These rocks, totally enclosed in mafic rocks with sharp and concordant contacts, show a magmatic lamination and follow the general NW–SE trend of QMUI. The apatite-rich ultramafic rocks makes up 90–95% of the total ultramafic outcrops and contain Mg-poor olivine (Mg# ∼ 40–58) and low-Mg spinel (Mg# ∼ 30–44) in contrast to apatite-poor ones (∼60–63 and ∼43–46, respectively). Field relationships, mineral compositions and geochemical data suggested that the FTP are not related to the mafic host rocks. On the contrary, they intruded latter into the gabbros during plastic, high temperature deformation in local shear zones. Fractional crystallization of P-rich ferrobasaltic parental magma at depth, probably in an open magmatic system, not far from the QMUI magma chamber, is considered as responsible for the formation of the evolved FTP in QMUI.  相似文献   

4.
Summary ?Post-magmatic garnets occur in volcanic breccias at the base of the Neapolitan Yellow Tuff (NYT) formation in the north-western area of the Phlegraean Fields. We report the results of a comprehensive study of these grandites. Garnet is found on the surfaces of tuffaceous blocks or inside their micropores, and is associated with sodalite, sanidine, marialite and amorphous silica. Garnet samples were examined by scanning electron microscopy (SEM), electron probe microanalysis (EPMA), powder and single-crystal X-ray diffraction (XRD) and infrared spectroscopy (IR). SEM observations on morphology showed typical dodecahedral and icositetrahedral habits. EPM analysis showed that they are close to grossular or andradite end members, with only moderate solid solution between them. X-ray study of single crystals showed cubic cell dimensions ao of 11.86 ? (grossular) and 12.04 ? (andradite). IR spectroscopy confirmed the presence of hydroxyls in coexisting garnet and sanidine, 0.06 wt% H2O (garnet) and 0.05–0.07 wt% H2O (sanidine), respectively. Well-crystallized sanidine of an earlier generation showed significantly higher water contents, in the range 0.13–0.23 wt% H2O. Type of occurrence and mineralogical features suggest a post-magmatic (pneumatolitic) genesis for these garnets. This is consistent with the physico-chemical processes linked to the eruptive dynamics of the breccias. Experimental studies of garnet synthesis at 550 °C and 2 kbar provide further support for this concept. Received January 16, 2002; accepted March 18, 2002  相似文献   

5.
Small hypabyssal intrusives of biotite pyroxenite and biotiteperidotite are described from part of theGardar alkaline province.The intrusives, composed essentially of diopside, olivine, phlogopiteand Fe-Ti oxides (and numerous accessory minerals) are inferredto have crystallized from silica-undersaturated ultramafic magmasof similar bulk composition. Crystallization occurred at anestimated depth of 3–4 km. Despite relatively rapid consolidation(probably attendant on a partial devolatilization) producingtypically fine-grained and sometimes porphyritic rocks, small-scaledifferentiation nevertheless occurred. The differentiates, asveins, pegmatoidal patches and roofing-facies tend to be olivine-poorphlogopite+ferriandiopside+ Fe-Ti oxide rocks, in which perovskite,andradite, apatite and sphene are significant components. Pyroxenecompositions in the ultramafites are consistent with the thesisthat the rocks formed from soda-deficient magmas in stronglyoxidizing conditions. Relative potassium enrichment (averageK2O: Na2O wt. % = 1.6) is expressed modally in the ubiquitouspresence of phlogopite and normatively by an average of 6.9%or and/or Ic. Despite compositional affinity with certain olivinemelilitites, melilite is absent, a fact that may be attributableto the comparatively high hydrostatic pressure (c. 1 kb) pertainingduring crystallization. Petrographic and geochemical evidencesuggests that the ultramafic magmas were residua after fractionationof forsteritic olivine from more magnesian magmas of kimberlitetype. It is proposed that the latter may in turn have been residuafrom eclogite fractionation of Fe-Ti rich primary magmas inthe upper mantle.  相似文献   

6.
The results of melt inclusion study are reported for chromites of the Klyuchevsky ultramafic massif, which is the most representative of all Ural ultramafic massifs localized beyond the Main Ural Fault Zone. The massif is composed of a dunite-harzburgite complex (tectonized mantle peridotite) and a dunite-wehrlite-clinopyroxenite-gabbro complex (layered portion of the ophiolitic section). The studied Kozlovsky chromite deposit is located in the southeastern part of the Klyuchevsky massif and hosted in serpentinized dunite as a series of lenticular bodies and layers up to 7–8 m thick largely composed of disseminated and locally developed massive ore. Melt inclusions have been detected in chromites of both ore types. The heated and then quenched into glass melt inclusions and host minerals were analyzed on a Camebax-Micro microprobe. The glasses of melt inclusions contain up to 1.06 wt % Na2O + K2O and correspond to melts of normal alkalinity. In SiO2 content (49–56 wt %), they fit basalt and basaltic andesite. The melt inclusions are compared with those from chromites of the Nurali massif in the southern Urals and the Karashat massif in southern Tuva. The physicochemical parameters of magmatic systems related to the formation of disseminated and massive chromite ores of the Klyuchevsky massif are different. The former are characterized by a wider temperature interval (1185–1120°C) in comparison with massive chromite ore (1160–1140°C).  相似文献   

7.
 The thermoelastic parameters of natural andradite and grossular have been investigated by high-pressure and -temperature synchrotron X-ray powder diffraction, at ESRF, on the ID30 beamline. The P–V–T data have been fitted by Birch-Murnaghan-like EOSs, using both the approximated and the general form. We have obtained for andradite K 0=158.0(±1.5) GPa, (dK/dT )0=−0.020(3) GPa K−1 and α0=31.6(2) 10−6 K−1, and for grossular K 0=168.2(±1.7) GPa, (dK/dT)0=−0.016(3) GPa K−1 and α0=27.8(2) 10−6 K−1. Comparisons between the present issues and thermoelastic properties of garnets earlier determined are carried out. Received: 7 July 2000 / Accepted: 20 October 2000  相似文献   

8.
In western part of the CEIM (Central-East Iranian Microcontinent) (Bayazeh area, Isfahan province, Iran), a series of Paleozoic basaltic rocks, occur. Major minerals of these basalts are olivine, clinopyroxene (diopside, augite), plagioclase (albite), sanidine, amphibole (kaersutite), phlogopite, ilmenite and magnetite. Secondary minerals include epidote, pumpellyite, albite, calcite and chlorite. Olivine and clinopyroxene are as phenocryst, while feldspars are restricted to groundmass. Chemical composition of clinopyroxenes indicates crystallization during ascending of magma. Geochemical analysis of whole rock samples shows that these rocks are characterized by low SiO2 (43.21–48.45 wt %), high TiO2 (1.81–3.00 wt %) and P2O5 (0.18–0.34 wt %). Petrography, chemistry of clinopyroxenes and whole rock analyses reveal an alkaline nature of these basalts. They are enriched in alkalis (Na2O + K2O = 4.1–7.7 wt %), LILE, HFSE and LREE. The Bayazeh alkali-basalts present strong enrichment in LREE relative to HREE (La/Lu ratio = 77.6–119.6) and were dominantly derived from partial melting of a metasomatized asthenospheric garnet-amphibole lherzolite. Field relationships reveal that junction of faults in west of the Bayazeh prepared a suitable path for ascending of magma from deep regions to surface and intra-plate continental magmatism. The Paleo-Tethys subduction from lower to upper Paleozoic is too enough for mantle enrichment in volatiles and basaltic alkaline magmatisrn in upper Paleozoic of Bayazeh area.  相似文献   

9.
The compression of synthetic pyrope Mg3Al2 (SiO4)3, almandine Fe3Al2(SiO4)3, spessartine Mn3Al2 (SiO4)3 grossular Ca3Al2(SiO4)3 and andradite Ca3Fe2 (SiO4)3 was studied by loading the crystals together in a diamond anvil cell. The unit-cell parameters were determined as a function of pressure by X-ray diffraction up to 15 GPa using neon as a pressure transmitting medium. The unit-cell parameters of pyrope and almandine were measured up to 33 and 21 GPa, respectively, using helium as a pressure medium. The bulk moduli, K T 0, and their first pressure derivatives, K T 0 ′, were simultaneously determined for all five garnets by fitting the volume data to a third order Birch-Murnaghan equation of state. Both parameters can be further constrained through a comparison of volume compressions between pairs of garnets, giving for K T 0 and K T 0 ′ 171(2) GPa and 4.4(2) for pyrope, 185(3) GPa and 4.2(3) for almandine, 189(1) GPa and 4.2 for spessartine, 175(1) GPa and 4.4 for grossular and 157(1) GPa and 5.1 for andradite, where the K T 0 ′ are fixed in the case of spessartine, grossular and andradite. Direct comparisons of the unit-cell volumes determined at high pressures between pairs of garnets reveal anomalous compression behavior for Mg2+ in the 8-fold coordinated triangular dodecahedron in pyrope. This agrees with previous studies concerning the compression behaviors of Mg2+ in 6-fold coordinated polyhedra at high pressures. The results show that simple bulk modulus–volume systematics are not obeyed by garnets. Received: 29 July 1998 / Revised, accepted: 7 April 1999  相似文献   

10.
 High-pressure and high-temperature Raman spectra of CaGeO3 tetragonal garnet have been collected to 11.5 GPa and 1225 K, respectively, in order to investigate possible intrinsic anharmonic behaviour in this phase. The Raman peak positions were observed to vary linearly with pressure and temperature within the ranges studied, with the higher-energy peaks showing larger P- and T-induced shifts than the low energy modes. The observed T-induced shifts are similar to those reported for grossular and andradite, while the observed P-induced shifts are generally larger than those of aluminosilicate and MgSiO3 majorite garnets (Gillet et al. 1992; Rauch et al. 1996) due to the larger bulk modulus of CaGeO3 garnet. The observed mode shifts of CaGeO3 garnet were used to determine the isothermal and isobaric mode Grüneisen parameters for this phase. These parameters are similar in value to those reported previously for grossular and andradite (Gillet et al. 1992). The calculated intrinsic anharmonic parameters, a i , for CaGeO3 garnet were determined to be nonzero, indicating significant anharmonic behaviour for this phase. These values, which range from −3.8 × 10−5 K−1 to −1.3 × 10−5 K−1, are also similar to those reported for andradite and grossular, but smaller than those determined for pyrope (Gillet et al. 1992). Hence, we expect MgSiO3 majorite to show greater anharmonicity than the germanate analogue studied by us. The anharmonic parameters determined for CaGeO3 tetragonal garnet may now be introduced into quasiharmonic vibrational heat capacity models to account for the observed anharmonic behaviour. Received: 21 April 1999 / Revised, accepted: 11 September 1999  相似文献   

11.
The investigation of stable and radiogenic isotopes and of platinum-group (PGE) and rare earth elements (REE) in chromitites and associated ultramafic rocks of the Kempirsai Massif, southern Urals, gives strong evidence for a multistage formation of giant ophiolitic-podiform chromite deposits present in the southeastern part of the massif. The Kempirsai ophiolite massif is divided by a shear zone into two parts: in the northwestern area, small bodies of Al-rich chromite formed from basaltic melts between 420 to 400 Ma, according to Sm-Nd mineral isochrons of harzburgite, pyroxenite, websterite and gabbro. Harzburgites and pyroxenites in this area are enriched in light REE and have ɛNd(400) > +6 and ɛSr(400) ∼ +5. Chromitites have scattered PGE distributions (Pd/Ir, 0.4–7.0), being partly enriched in Pd and Pt. γOs(400) of one chromitite is −4.4. The southeastern part of the Kempirsai Massif, well-known for its world-class deposits of podiform low-Al magnesiochromite, is characterized by harzburgite and dunite enriched in light REE with very low ɛNd(400) (+4.3 to –17.1) and positive ɛSr(400) (>+10) values. Chromitites are strongly enriched in Ir, Os and Ru and depleted in Pd and Pt. γOs(400) of three chromitites is uniform and approaches C1 and DMM compositions. In veins and pods postdating crystallization of massive chromite, pargasitic amphibole formed in equilibrium with fluid-inclusion-bearing chromite at temperatures close to 1000 °C. These amphiboles give 40Ar/39Ar stepwise heating ages of 365 to 385 Ma and are characterized by low ɛNd(400) (+0.6 to −4.6) and general enrichment in REE. The cooling ages correspond to a 379.3 ± 1.6 Ma Rb-Sr mineral isochron produced from amphibole and phlogopite of a pyroxenite vein in the western part of the massif. From these data it is concluded that parts of the Kempirsai Massif have been pervasively metasomatized by large amounts of fluids and melts derived from a subducted slab composed of oceanic crust and sediments. Subduction occurred at least 15–35 Ma after a melting event that produced a typical ophiolitic sequence in the Paleozoic Sakmara Zone. We conclude that large chromite orebodies formed from second-stage high-Mg melts that interacted with depleted mantle and fluids on their way upward in a suprasubduction zone regime, and in a fore-arc position to the Magnitogorsk island arc. Received: 21 January 1998 / Accepted: 24 August 1998  相似文献   

12.
This contribution addresses contact metamorphism and fluid flow in calcareous rocks of the Neoproterozoic Shaler Supergroup on Victoria Island, Arctic Canada. These processes occurred due to intrusion of gabbroic sills and dykes at c. 720 Ma during the Franklin magmatic event, which was associated with the break‐up of Rodinia. The intrusive sheets (sills and dykes) are a few metres to ～50 m thick. Metasedimentary rocks were examined in three locations with very good exposures of vertical dykes feeding horizontal sills, the Northern Feeder Dyke (NFD) complex, the Southern Feeder Dyke (SFD) complex and the Uhuk Massif. In the NFD and SFD complexes, protoliths were limestones and dolostones with minor silicates, and at the Uhuk Massif, the protoliths were silty dolostones. At the time of magma emplacement, these locations were at depths of 1–4 km. The widths of contact aureoles are only several decametres wide, commensurate with thicknesses of the dykes and sills. Splays of tremolite mark incipient metamorphism. Highest grade rocks in the NFD and SFD complexes contain the prograde assemblage diopside + phlogopite whereas at Uhuk they contain the assemblage vesuvianite + garnet + diopside. The assemblages are successfully modelled with T–X(CO2)fluid pseudosections that suggest achievement of CO2‐rich fluid compositions due to early decarbonation reactions, followed by influx of aqueous fluids after peak metamorphism. Rapid heating of host rocks and short near‐peak temperature intervals are demonstrated by the prevalent morphology of diopside as radial splays of acicular crystals that appear to pseudomorph tremolite and by incomplete recrystallization of calcite in marbles. Calcsilicates in the roof of one sill at Uhuk experienced metasomatic influx of Fe that is evidenced by nearly pure andradite rims on grossular garnet. Vesuvianite, which overgrew the grossular portions of garnet, also contains ferric iron. Vesuvianite was partially consumed during retrograde growth of serpentine and andradite. The occurrence of serpentine in high‐grade portions of aureoles is consistent with eventual levelling‐off of temperatures between 350 and 400 °C, an inference that is supported by modelled conductive heat transfer from the cooling magma sheets. Focused fluid flow near intrusion‐wall rock contacts is demonstrated by narrow zones of anomalously low δ13C and δ18O values of carbonate minerals. Although the up to 5‰ decrease of both δ13C and δ18O values from sedimentary values is much smaller than is typical for calcsilicate aureoles around large plutons, it is greater than what could have been achieved by decarbonation alone. The decrease in δ13C is attributed to fluid‐mediated exchange with organic low‐13C carbon that is dispersed through the unmetamorphosed rocks and the decrease in δ18O is attributed to fluid‐mediated isotopic exchange with the gabbroic intrusive sheets. This study shows that when gabbroic sills and dykes intrude a sedimentary basin, (i) contact aureoles are likely to be narrow, only on the scale of several decametres; (ii) short high‐temperature regimes prevent achievement of equilibrium metamorphic textures; and (iii) T–X(CO2)fluid paths in calcareous contact aureoles are likely to be complex, reflecting a transition from prograde decarbonation reactions to influx of aqueous fluids during cooling.  相似文献   

13.
The equilibrium phase relations of a mafic durbachite (53 wt.% SiO2) from the Třebíč pluton, representative of the Variscan ultrapotassic magmatism of the Bohemian Massif (338–335 Ma), have been determined as a function of temperature (900–1,100°C), pressure (100–200 MPa), and H2O activity (1.1–6.1 wt.% H2O in the melt). Two oxygen fugacity ranges were investigated: close to the Ni–NiO (NNO) buffer and 2.6 log unit above NNO buffer (∆NNO + 2.6). At 1,100°C, olivine is the liquidus phase and co-crystallized with phlogopite and augite at 1,000°C for the whole range of investigated pressure and water content in the melt. At 900°C, the mineral assemblage consists of augite and phlogopite, whereas olivine is not stable. The stability field of both alkali feldspar and plagioclase is restricted to low pressure (100 MPa) at nearly water-saturated conditions (<3–4 wt.% H2O) and T < 900°C. A comparison between experimental products and natural minerals indicates that mafic durbachites have a near-liquidus assemblage of olivine, augite, Ti-rich phlogopite, apatite and zircon, followed by alkali feldspar and plagioclase, similar to the mineral assemblage of minette magma. Natural amphibole, diopside and orthopyroxene were not reproduced experimentally and probably result from sub-solidus reactions, whereas biotite re-equilibrated at low temperature. The crystallization sequence olivine followed by phlogopite and augite reproduces the sequence inferred in many mica-lamprophyre rocks. The similar fractionation trends observed for durbachites and minettes indicate that mafic durbachites are probably the plutonic equivalents of minettes and that K- and Mg-rich magmas in the Bohemian Massif may have been generated from partial melting of a phlogopite–clinopyroxene-bearing metasomatized peridotite. Experimental melt compositions also suggest that felsic durbachites can be generated by simple fractionation of a more mafic parent and mixing with mantle-derived components at mid crustal pressures.  相似文献   

14.
The massif-type anorthosite complex at Bolangir in the northern part of the Eastern Ghats belt occurs in a milieu of predominantly supracrustal granulite-grade rocks. The massif is separated from the host gneisses by coarse-grained garnetiferous granitoid gneisses which are interpreted as coeval crustallyderived melts. Melanocratic ferrodiorite rocks occur at the immediate contact with the anorthosite massif which they intrude in cross-cutting dikes and sheets. The emplacement age of the anorthosite diapir and the associated igneous suites is deemed to be pre-D2. Recrystallization of the igneous assemblages of the ferrodiorite suite (750–800°C, 7–8kbar, ) during a period of near-isobaric cooling from the igneous crystallization stage to the regionalP-T regime led to extensive development of coronitic garnet at the interface of plagioclase phenocrysts with the mafic matrix assemblage (opx + fay + cpx + ilm ± amph, bio). Abundant accessory phases are zircon, apatite and thorite. The mafic phases have extremely ferrous compositions (XFe gar: 0.93-0.87, fay: 0.90-0.87, opx: 0.80-0.60, cpx: 0.70-0.47, amph: 0.81-0.71) reflecting the low Mg-number (16-8) of the rocks. Compared to worldwide occurrences of similar rocks, the Bolangir ferrodiorites (SiO2 36–58 wt.%, FeO*: 39-10 wt.%) are characterized by exceptionally high concentrations of HFSE and REE (TiO2: 4.8-1.0 wt.%, P2O5: 1.7-0.5 wt.%, Zr: 5900-1300 ppm, Y: 240-80 ppm, La: 540-100 ppm, Ce: 1100-200 ppm, Yb: 22-10 ppm, Th: 195-65 ppm). Well defined linear variation trends for major and trace elements reflect progressive plagioclase accumulation towards the felsic members of the suite. The ferrodiorites are interpreted to represent residual liquids of anorthosite crystallization which after segregation and extraction from the ascending diapir became enriched in HFSE and REE through selective assimilation of accessory phases (zircon, monazite, apatite) from crustal felsic melts. Ferromonzodioritic rock presumably formed through hybridization between the ferrodiorite and overlying felsic melts.  相似文献   

15.
Almost pure andradite and intermediate members of the andradite-grossular series (gros40–49, and 47–54, py0–3, alm0–3, spess0–2, hydrogarnet0–3), often framboidal in habit, are widespread in metabasites including lavas, minor intrusions, and volcanic sandstones and breccias metamorphosed under prehnite-pumpellyite and pumpellyite-actinolite facies conditions, possibly extending into the zeolite facies. Coexisting phases include iron-rich epidotes (100 Fe*/Fe*+Al=22–34), pumpellyite, prehnite, actinolite, and chlorite, electron microprobe analyses of which are given, as well as quartz, albite, and calcite. Zoisite (100 Fe*/Fe*+Al=1–5) and iron-poor epidote (100 Fe*/Fe*+Al=11–18) occur in 2 rocks in pseudomorphs after plagioclase together with more iron-rich epidote, but not in close association with the garnets. Coexisting pumpellyite is iron-rich (FeO* 9–14%) in the prehnite-pumpellyite facies and iron-poor (FeO* 5%) in the pumpellyiteactinolite facies. Chlorites and actinolites vary widely and sympathetically in FeO/MgO+FeO ratio. Andradite is also described from a stilpnomelane-actinolite-hematite-bearing andradite quartzite of the pumpellyite-actinolite facies. Conditions of formation involved temperatures of 300 to 400 ° or less, at pressures up to a few kilobars. A wide range of oxygen fugacities is possible, but in the fluid phase was low. Grandite and chlorite are incompatible in the pumpellyite-actinolite and greenschist facies in the presence of quartz but the 2 minerals occur together in some pumpellyite-actinolite facies assemblages as a result of incomplete reaction and/or local deficiency in silica. In the greenschist facies the association is replaced by epidote-actinolite±hematite and sodic amphibole. Whereas at medium to high grades of metamorphism andradite and grandite are characteristic of skarns irrespective of , at very low grades they are found in mafic volcanic rocks and volcanogenic sediments as well as in certain cherty rocks of unusual composition, rodingites, and serpentinites, where was very low.  相似文献   

16.
Summary ?In order to evaluate the stability of Mg–Ca garnets at P = 2.5 GPa/T = 800–1500 °C, some experiments were performed using both natural and synthetic starting materials. Particular attention was paid to the investigation of the Ca rich side of the pyrope–grossular join and the maximum pyrope content in grossular was found to be about 10 mol.%. The addition of Cr to the system only slightly increases the observed pyrope solubility in grossular whereas Na stabilises melilite and merwinite. Clinopyroxene with a composition lying on the diopside – Ca Tschermak join appears to be the only stable crystalline phase in the middle part of the pyrope–grossular join. Received August 28, 2001; revised version accepted July 23, 2002 Published online February 24, 2003  相似文献   

17.
Summary We have conducted electron microprobe (EMP) analysis of 158 grains of platinum-group minerals (PGM; 0.1–1 mm in size) from 11 placer samples collected from Holocene fluvial placers and buried paleochannel placers at various localities in British Columbia. These grains principally comprise Pt-Fe-(Cu) alloy minerals: Fe-rich platinum [ΣPGE:(Fe + Cu + Ni) = 3.6–7.6], Pt3Fe-type alloy (isoferroplatinum or Fe-rich platinum), subordinate “Pt2Fe”-type alloy (probably, a compositional variant of Fe-rich platinum) and the tulameenite-tetraferroplatinum series. Less-abundant are iridium [Ir-dominant Ir-Os-(Pt) alloy] and osmium [Os-dominant Os-Ir-(Pt) alloy]. Ruthenium [Ru-dominant Ru-Ir-Os alloy] occurs as a single grain. One of these Pt-Fe alloy grains is unusually zoned; its core zone is: Pt74.0Fe20.4Cu1.9Ir1.5Rh1.1Pd1.0Os0.08Ru0.01Ni0.01 (in at%) [ΣPGE:(Fe + Cu + Ni) = 3.5], and its rim zone is: Pt78.5Fe15.5Cu1.7Ir1.5Rh1.4 Pd1.2Ni0.15Os0.06Ru<0.01 [ΣPGE:(Fe + Cu + Ni) = 4.8]. This zoning indicates late-stage removal of Fe and corresponding addition of Pt, probably as a result of interaction with a late fluid phase. Various combinations of minor elements: Ir-Rh, Rh-Pd, and Ir-Rh-Pd are observed in the analysed Pt-Fe-Cu alloys. However, the Ir-Pd pair appears to be prohibited because of crystallochemical factors. Minute PGM inclusions in Pt-Fe alloy grains, likely derived from the Tulameen complex, comprise: hongshiite (Pt1.04Pd0.02 Cu0.93), sperrylite (Pt0.93Ir0.03)Σ0.96(As2.02Sb0.01)Σ2.03, hollingworthite-platarsite (Rh0.74 Pt0.21Fe0.02Pd0.02Ir0.01)Σ1.00S0.91As1.10, cuprorhodsite-malanite (Cu0.91Fe0.03Ni<0.01)Σ0.95 (Rh1.06Pt0.89Ir<0.01)Σ1.95S4.10, a rare Te-rich isomertieite (Pd10.96Fe0.03)Σ10.99(Sb1.13 Te0.94)Σ2.07As1.93, and an unusual Pt-Pd-Rh antimonide [(Pt + Pd + Rh):(Sb + As) = 1.2–1.25], related to genkinite. This antimonide may exhibit a minor solid solution extending from genkinite toward stumpflite. In addition, 20 grains of diopside [Ca46.4–49.1Mg42.8–48.2Fe3.1–8.1; ≤0.59 wt% Cr2O3] and 20 grains of olivine [Fo86.8–91.5 Fa7.9–12.5], from a PGM-bearing placer located in the vicinity of the Tulameen complex, were analysed. The compositional ranges of these placer silicates are comparable to those of clinopyroxene and olivine in the olivine clinopyroxenite and dunite units of the Tulameen complex. The majority of the analysed placer PGM grains were probably derived from Alaskan-type source rocks, whereas an ophiolitic source, associated with the Atlin ophiolite complex, is suggested for the placer PGM deposits in the Atlin area, northern British Columbia. Authors’ addresses: Andrei Y. Barkov, Robert F. Martin, Department of Earth and Planetary Sciences, McGill University, 3450 University Street, Montreal, Quebec H3A 2A7, Canada; Michael E. Fleet, Department of Earth Sciences, University of Western Ontario, London, Ontario, N6A 5B7, Canada; Graham T. Nixon and Victor M. Levson, B.C. Geological Survey, Ministry of Energy, Mines and Petroleum Resources, PO Box 9320 Stn. Prov. Govt., Victoria, British Columbia V8W 9N3, Canada  相似文献   

18.
Titanium in phengite: a geobarometer for high temperature eclogites   总被引：1，自引：1，他引：0  
Phengite chemistry has been investigated in experiments on a natural SiO2–TiO2-saturated greywacke and a natural SiO2–TiO2–Al2SiO5-saturated pelite, at 1.5–8.0 GPa and 800–1,050°C. High Ti-contents (0.3–3.7 wt %), Ti-enrichment with temperature, and a strong inverse correlation of Ti-content with pressure are the important features of both experimental series. The changes in composition with pressure result from the Tschermak substitution (Si + R2+ = AlIV + AlVI) coupled with the substitution: AlVI + Si = Ti + AlIV. The latter exchange is best described using the end-member Ti-phengite (KMgTi[Si3Al]O10(OH)2, TiP). In the rutile-quartz/coesite saturated experiments, the aluminoceladonite component increases with pressure while the muscovite, paragonite and Ti-phengite components decrease. A thermodynamic model combining data obtained in this and previous experimental studies are derived to use the equilibrium MgCel + Rt = TiP + Cs/Qz as a thermobarometer in felsic and basic rocks. Phengite, rutile and quartz/coesite are common phases in HT-(U)HP metamorphic rocks, and are often preserved from regression by entrapment in zircon or garnet, thus providing an opportunity to determine the T–P conditions of crystallization of these rocks. Two applications on natural examples (Sulu belt and Kokchetav massif) are presented and discussed. This study demonstrates that Ti is a significant constituent of phengites that could have significant effects on phase relationships and melting rates with decreasing P or increasing T in the continental crust.  相似文献   

19.
秦岭造山带内的山阳-柞水古生代弧前盆地中出露有池沟、小河口、冷水沟、园子街、下官坊及双元沟等CuMo、CuFe(Au)矿床,与这些矿床具有成因联系的岩体为形成于150~140Ma的高钾钙碱性和钾玄岩系列花岗岩,为华北和扬子大陆碰撞后伸展阶段壳、幔混合岩浆的产物。矿化主要发生在岩体与泥盆、石炭纪地层中碳酸盐岩的接触带附近,主要类型为矽卡岩型,少量为斑岩型,部分矿床具有统一的矽卡岩-斑岩型成矿系统,矿化组合主要为CuMo、CuFe(Au)和Cu矿化。外接触带主要发育有矽卡岩和角岩化蚀变,内接触带主要为岩体内部的硅化、钾化、绢云母化、绿泥石化及粘土化,内矽卡岩不发育。矽卡岩矿物主要有石榴石、透辉石、绿帘石、透闪石,阳起石等,其中石榴子石主要为钙铁榴石和钙铝榴石,透辉石是辉石的主体,早期形成的石榴石和透辉石等无水矿物组合常被后期的绿帘石、透闪石和阳起石等含水矿物及石英、方解石等所交代。金属矿物比较简单,最主要的含铜矿物为黄铜矿和斑铜矿,铁矿化主要为磁铁矿和镜铁矿。尽管这些矿床以矽卡岩型矿化为主,但部分矿床中已发现有斑岩型矿化和蚀变特征,这可能暗示了该区可能具有统一的矽卡岩-斑岩型成矿系统,进而表明山阳-柞水矿集区深部具有寻找斑岩型矿床的巨大潜力。  相似文献   

20.
A critical study of 311 published WR chemical analyses, isotopic and mineral chemistry of anorthosites and associated rocks from eight Proterozoic massif anorthosite complexes of India, North America and Norway indicates marked similarities in mineralogy and chemistry among similar rock types. The anorthosite and mafic-leucomafic rocks (e.g., leuconorite, leucogabbro, leucotroctolite, anorthositic gabbro, gabbroic anorthosite, etc.) constituting the major part of the massifs are characterized by higher Na2O + K2O, Al2O3, SiO2, Mg# and Sr contents, low in plagioclase incompatible elements and REE with positive Eu anomalies. Their δ 18O‰ (5.7–7.5), initial 87Sr/86Sr (0.7034–0.7066) and ɛ Nd values (+1.14 to +5.5) suggest a depleted mantle origin. The Fe-rich dioritic rocks occurring at the margin of massifs have isotopic, chemical and mineral composition more close to anorthosite-mafic-leucomafic rocks. However, there is a gradual decrease in plagioclase content, An content of plagioclase and XMg of orthopyroxene, and an increase in mafic silicates, oxide minerals content, plagioclase incompatible elements and REE from anorthosite-mafic-leucomafic rocks to Fe-rich dioritic rocks. The Fe-rich dioritic rocks are interpreted as residual melt from mantle derived high-Al gabbro melt, which produced the anorthosite and mafic-leucomafic rocks. Mineralogically and chemically, the K-rich felsic rocks are distinct from anorthosite-mafic-leucomafic-Fe-rich dioritic suite. They have higher δ 18O values (6.8–10.8‰) and initial 87Sr/86Sr (0.7067–0.7104). By contrast, the K-rich felsic suites are products of melting of crustal precursors.  相似文献   

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