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1.
Topaz granite is alkali-feldspar granite that contains essential albite, quartz, K-feldspar, lithium-mica, and topaz. As a group topaz granites are characterized by their extreme enrichment in F (up to 3 wt%) and a wide variety of lithophile elements. They can be subdivided into a 'low-P2O5 subtype' (P2O5 < 0.1 wt%, Al2O3 < 14.5 wt%, SiO2 > 73 wt%) and a 'high-P2O5 subtype' (P2O5 > 0.4 wt%, Al2O3 > 14.5 wt%, SiO2 < 73 wt%), the δ18O values of which indicate a dichotomy of source rock: the low-P2O5 subtype (δ18O < 10‰) having a meta-igneous protolith and the high-P2O5 subtype (δ18O > 10 ‰) a source with a significant component of pelitic material. The unusually high F contents enhance the efficacy of melt segregation and crystal-melt fractionation and so facilitate extreme differentiation in topaz granite magmas. Very low melt volumes restrict the bulk composition of the partial melts regardless of the nature of the source; and extreme fractionation forces them along a path of magmatic convergence, to produce a group of granitic rocks with near-minimum compositions so enriched in a variety of lithophile elements (Li, Nb, Ta, Sn) that economic mineralization often results.  相似文献   

2.
Abstract: Ilmenite, hematite, garnet, monazite, zircon, rutile, magnetite, sillimanite, pyroxene and amphibole from the beach sands of Ekakula, Gahiramatha coast, Orissa, India are reported here for the first time. Their total concentration varies from 26. 4 to 100%. Ilmenite, monazite and zircon are between 100 and 300 um in size and are well rounded in shape. Ilmenite-hematite intergrowth is common. Ilmenite has 50. 02–54. 73% TiO2, 42. 42–46. 90% FeO (total Fe) and small amounts of Al, Mn, Mg, Ca, Ba, Si, V, Cr, and Zn. The bulk samples contain 10. 63–41. 42 % TiO2, 6. 15–26. 07 % FeO, 5. 86–16. 75 % Fe2O3, 7. 41–61. 74 % SiO2, 1. 39–12. 83% A12O3, 0. 32–4. 97% CaO, 0. 53–4. 24% P2O5, 0. 17–3. 27% MgO, 0. 15–2. 97% Na2O, 0. 07–2. 34% K2O, and 0. 05–0. 71% V2O5 together with appreciable amounts of La, Ce, Pr, Nd, Sm, Eu, Y, U, Th, Zr, and trace amounts of Pb, Zn, Cu, Ni, Co, and Cr. Khondalite, charnockite, calc-silicate granulite, leptynite, migmatite, gneiss, basic granulite and pegmatite of the Eastern Ghats appear to be the major source for the above heavy mineral assemblages. The samples are amenable to gravity and magnetic methods of beneficiation.  相似文献   

3.
Abstract In granulite facies metapelitic rocks in the Musgrave Complex, central Australia, reaction between S1 garnet and sillimanite involves the development in S2 of both garnet + cordierite + hercynitic spinel + biotite and hercynitic spinel + cordierite + sillimanite + biotite. The S2 assemblages occur either in coronas and symplectites, mainly around garnet, or, in rocks in which S2 is more strongly developed, as recrystallized assemblages. Ignoring the presence of biotite and ilmenite, the mineral textures can be accounted for qualitatively by a consideration of the model system FeO-MgO-Al2O3-SiO2 (FMAS); the textural relationships accord with decompression accompanying the change from S1 to S2. However, since biotite and ilmenite are involved in the assemblages, the parageneses are better accounted for in terms of equilibria in the expanded model system K2O-FeO-MgO-Al2O3-SiO2-H2-TiO2-Fe2O3 (KFMASHTO), i.e. AFM + TiO2+ Fe2O3. The coronas reflect the tectonic unroofing of at least part of the Musgrave Complex from peak S1 conditions of about 8 kbar to S2 conditions of about 4 kbar.  相似文献   

4.
Magnesian metapelites of probable Archaean age from Forefinger Point, SW Enderby Land, East Antarctica, contain very-high-temperature granulite facies mineral assemblages, which include orthopyroxene (8–9.5 wt% Al2O3)–sillimanite ± garnet ± quartz ± K-feldspar, that formed at 10 ± 1.5 kbar and 950 ± 50°C. These assemblages are overprinted by symplectite and corona reaction textures involving sapphirine, orthopyroxene (6–7 wt% Al2O3), cordierite and sometimes spinel at the expense of porphyroblastic garnet or earlier orthopyroxene–sillimanite. These textures mainly pre-date the development of coarse biotite at the expense of initial mesoperthite, and the subsequent formation of orthopyroxene (4–6 wt% Al2O3)–cordierite–plagioclase rinds on late biotite.
The early reaction textures indicate a period of near-isothermal decompression at temperatures above 900°C. Decompression from 10 ± 1.5 kbar to 7–8 kbar was succeeded by biotite formation at significantly lower temperatures (800–850°C) and further decompression to 4.5 ± 1 kbar at 700–800°C.
The later parts of this P–T evolution can be ascribed to the overprinting and reworking of the Forefinger Point granulites by the Late-Proterozoic ( c . 1000 Ma) Rayner Complex metamorphism, but the age and timing of the early high-temperature decompression is not known. It is speculated that this initial decompression is of Archaean age and therefore records thinning of the crust of the Napier Complex following crustal thickening by tectonic or magmatic mechanisms and preceding the generally wellpreserved post-deformational near-isobaric cooling history of this terrain.  相似文献   

5.
Arenites in the low-grade metasedimentary rocks of the Stirling-Barren Group, Western Australia, contain discrete spaced cleavages. These in part are pure white mica, but up to 30% of the cleavage zones consists of fine-grained quartz resulting from crystal plastic deformation. A modified Gresens analysis shows that the cleavage domains formed by a 50% volume loss associated primarily with SiO2 and MgO concentration decreases of 58% and 37%, respectively, and a 12% decrease in Fe2O3. Mössbauer spectroscopy shows that the Fe2+: Fe3+ ratio from lithon to cleavage changed from 50:SO to 15:85. This substantial difference cannot be accounted for by loss of iron. The data are best explained by the focusing of a highly oxidizing fluid through the cleavage domains where volumetric fluid rock ratios around 150 to 1 are indicated. In this example advectic processes appear to be important in low-grade regional metamorphism.  相似文献   

6.
A ternary solid solution model for omphacite with the end-members jadeite (NaAlSi2O6), diopside (CaMgSi2O6) and hedenbergite (CaFeSi2O6) was derived from experimental data from the literature. The subregular solution model, fitted by linear programming, is best suited to omphacites with very little aegirine component in common eclogites. Applying this solution model to the calculation of equilibrium phase diagrams of eclogites from the Adula nappe (Central Alps, Switzerland) results in large stability fields for common eclogite assemblages (garnet+omphacite+quartz+H2O±kyanite). Within this field the compositions of garnet and omphacite show very little variation. A precise determination of the peak-pressure and temperature is not possible. The occurrence of amphibole, overgrowing the peak-pressure assemblage in fresh eclogite, suggests retrograde re-equilibration, still under eclogite facies conditions. The computation of isopleths for garnet and pyroxene end-members allows the estimation of the pressure and temperature conditions of this re-equilibration event (19–21  kbar, c .  700 °C).  相似文献   

7.
New data from a geochemical, geochronological and isotopic study of the Late Precambrian Timna igneous complex suggest the formation of alkali granites from a LIL-enriched, mantle derived, sanukitoid-type monzodiorite (a silica oversaturated rock with Mg# >60). These data also provide new insights into the petrology, timing and regional tectonic control of the transition from the calc-alkaline to the alkaline magmatic activity in the northern Arabian-Nubian Shield (ANS) during the Late Precambrian.

The Timna alkali granite was formed by fractional crystallization from the monzodioritic magma in a quasi-stratified magmatic cell which formed 610 Ma ago in the 625 Ma old calc-alkaline, porphyritic granite crust. These monzodiorites are mantle-derived, as demonstrated by their high Mg# (63), Cr (230 ppm), and Ni (120 ppm). They are characterized by initial 87Sr/86Sr of 0.7034, ε-Nd (610 Ma) = +3.4, and are enriched in K2O (2.9%), Sr (840 ppm), Ba (1290 ppm) and LREE [(La/Lu)n= 10–25]. The chemical characteristics and REE patterns of the monzodiorites and andesitic dykes of Timna are very similar to Dokhan andesites from northeastern Egypt and the Archean sanukitoids from Canada. The isotopic, geochemical and geochronologic data all indicate that Timna monzodiorites are comagmatic with the alkali granite. The alkali granite is a typical post-orogenic, borderline A-type granite. It is enriched in potassium (K2O=4.68–6.64%), has a negative europium anomaly (Eu/Eu*=0.058–0.38) and ε-Nd (610 Ma) of +3.9. The calc-alkaline granite is a typical I-type granite with a small positive europium anomaly (Eu/Eu*=1.02–1.16). Its age and the Sr, Nd and Pb isotopic characteristics with ε-Nd (625 Ma) of +5.6 to +5.9 are significantly different from these of the alkali granite and monzodiorites, and indicate little interaction with the monzodiorite during the formation of the alkali granite.

The alkali granites are correlative with the post-collisional extensional granites in Jordan and Egypt while the porphyritic granites can be correlated with the late orogenic types. Crustal thickening associated with orogenic compression resulted in crustal anatexis to form the I-type granitic rocks, whereas crustal thinning associated with extension allowed LIL-enriched mantle melts to rise very near to the surface, where space was available for these to pond and fractionate to alkali granite.  相似文献   


8.
The proposed geothermobarometer is based on an empirical calibration which takes account of two equilibria involving the tremolite, edenite, pargasite and hastingsite components in amphiboles. It has applications to assemblages found in metabasic rocks of widely different chemical compositions (magnesian to Fe-rich metabasalts), and for metamorphism ranging from lower greenschist to highest amphibolite facies. Knowing the Si(T1), Aliv, Alvi, Fe3+, Fe2+, Mg, Ca, NaM4, NaA and A vacancy in an amphibole, and the Al3+ and X Mg in coexisting epidote and chlorite, it is possible to calculate two values of In K d for this assemblage. These equilibria involve edenite-tremolite and (pargasite/hastingsite)-tremolite end-members in amphibole (the calculation program is given). For these equilibria, the isopleths (iso-values of K d) have been calculated for 0.27 < X Mg < 0.75 and 0 < X Fe3+= Fe3+/(Fe3++ Alvi) < 0.8. It is then possible to determine pressure and temperature directly when X Mg, X Fe3+, In K d for tremoliteedenite and In K d for (pargasite/hastingsite)-tremolite are known. Application of this geothermobarometer is limited to Ca-free plagioclase assemblages, and complete P–T paths can be drawn only if all the minerals are considered together. Phase relations at successive stages of crystallization can be constrained by studying the relationships between the coexisting minerals, their zoning and the metamorphic fabrics.  相似文献   

9.
A second natural occurrence of yoderite   总被引：3，自引：0，他引：3  
A second example of yoderite has been discovered in whiteschists from the Southern Chewore Hills of northern Zimbabwe. The mineral is pale green in colour and occurs in an equilibrium assemblage with talc+chlorite+kyanite+dravite+hematite. There is no quartz present. Recalculated microprobe analyses give a structural formula of Mg2Al5.7Fe0.3Si4O18(OH)2, similar to that obtained for the type locality at Mautia Hill, Tanzania, i.e. Mg2Al5.6Fe0.4Si4O18(OH)2. Textural relationships and relative proportions of minerals suggest that the yoderite was formed by reaction between talc, chlorite, kyanite and hematite. Experimental evidence suggests high-water-pressure metamorphic conditions at temperatures exceeding a reaction curve that extends between 13  kbar at 590  °C and 21  kbar at 650  °C. The yoderite-bearing whiteschist is associated with a 1.4  Ga dismembered ophiolite. It is proposed that this yoderite occurrence is associated with a relict subduction/suture zone.  相似文献   

10.
In order to determine whether gas (steam) containing a small amount of dissolved alkali chloride is effective in promoting base exchange of Na+ and K+ among alkali feldspars and coexisting brine or brine plus solid salt, experiments were carried out at 400–700°C and steam densities ranging down to less than 0.05. For bulk compositions rich in potassium, the low pressure results are close to previous high-pressure results in composition of the fluid and coexisting solid phase. However, when the bulk composition is more sodic, alkali feldspars are relatively richer in potassium at low pressure than at high pressure. This behaviour corresponds to enrichment of potassium in the gas phase relative to coexisting brine and precipitation of solid NaCl when the brine plus gas composition becomes moderately sodic.

The gas phase is very effective in promoting base exchange between coexisting alkali feldspars at high temperature and low water pressure. This suggests that those igneous rocks which contain coexisting alkali feldspars out of chemical equilibrium either remained very dry during the high-temperature part of their cooling history or that the pore fluid was a gas containing very little potassium relative to sodium.  相似文献   


11.
Abstract A deerite-bearing rock occurs at the boundary between quartzite and metabasites within the 'schistes lustrés'of eastern Corsica. It contains the typomorphic assemblage pyroxene, blue amphibole, hematite and magnetite. Pyroxene shows homogeneous composition close to the aegirine end-member and blue amphibole is zoned from crossite core to riebeckite rim. The bulk chemical analysis of the rock is remarkable by its very high iron content and the presence of an unusually large amount of Zn which is concentrated in both deerite and amphibole. Electron microprobe analyses of the Corsican deerite are compared with those published in the literature; as shown by deerite from the Fransciscan iron formation, the principal substitution for Fe2+ is Mn whereas the amount of substitution for Fe3+ is low. In the system SiO2-FeO-Fe2O3-Al2O3-Na2O-MgO-H2O the typomorphic paragenesis can be described by an univariant reaction interpreted as the result of a pressure decrease. P-T conditions of metamorphism, previously estimated to be 8 kbar and 300°C, are in good agreement with present knowledge of the deerite stability field. The occurrence of hematite and magnetite in equilibrium permits an estimation of the oxygen fugacity (log f o2= -29.41 bar). Oxidation conditions are higher than those previously mentioned in the literature for similar assemblages.  相似文献   

12.
SHRIMP锆石U-Pb年龄测定表明,辽东半岛弟兄山岩体的侵位时代为三叠纪（205.2±2.1 Ma）,是华北东部三叠纪花岗岩的一部分.全岩岩石化学分析结果显示,弟兄山花岗岩具有高SiO2、Al2O3、K2O,低TiO2、Na2、MnO和CaO的特征,K2O+Na2变化范围为7.88%~9.28%,K2O/Na2 ≥ 1.16~1.46;CaO/Na2=0.08~0.23,铝指数A/CNK=0.95~1.10,并且在矿物组合中出现白云母,属准铝-过铝质花岗岩.在SiO2-Zr图解中,所有样品点均落在S型花岗岩区域中.以上特征均显示该花岗岩为准铝-过铝质S型花岗岩.稀土曲线和稀土参数表现出强烈的轻、重稀土分异特征和明显的Eu负异常特征,反映源区岩浆形成后发生过斜长石或其他富Ca矿物的分离结晶作用,是典型准铝-过铝质花岗岩的稀土元素特征.在原始地幔标准化的微量元素蛛网图上,所有花岗岩均富集Rb、Th,明显亏损Nb、Ta、Sr和Ti.所有样品的Rb=133×10-6~360×10-6,绝大多数样品高于花岗岩的平均值（200×10-6）;Sr（25×10-6~135×10-6）和Ba（48×10-6~507×10-6）明显低于花岗岩的平均值（Sr 300×10-6,Ba 830×10-6）,Ba、Sr亏损反映岩浆经历了较为完全的分离结晶作用;大离子亲石元素Rb、Th富集,Nb和Ta亏损显示陆壳物质为岩浆的源岩.上述特征表明岩浆物质来源于陆源碎屑岩石.结合区域构造演化历史,认为弟兄山岩体是库拉-太平洋板块向欧亚大陆俯冲的产物,是印支晚期华北岩石圈处于弱伸展状态背景的响应.  相似文献   

13.
Abstract. Vein type tungsten mineralization at Degana is genetically and spatially associated with the Degana Granite. The deposit is characterized by pervasive wall rock alteration around the mineralized quartz veins. Laterally three different alteration zones, greisen, silicification and potassic zones, are marked based on the field features, mineral assemblages and geo-chemical characteristics. In the present paper, systematic mineralogical and chemical variation in these alteration zones is reported. Thick mono-mineralic (zinnwaldite) selvages around the veins characterize the deposit. Plagioclase and alkali feldspar are low in the greisen zones while K-feldspar shows more increase than plagioclase in the potassic zone. Quartz is uniformly high in all the alteration zones, but it shows an anomalous value in the silicification zone. Al2O3 concentration shows initial depletion in greisen zone with gradual increase away from the contact. MgO and FeO are higher in greisen zone than silicification and potassic zones. The potassic zone is characterized by the depletion of Na2O and higher value of K2O.
The common presence of topaz and fluorite as both primary and secondary minerals and fluorine-bearing micas suggest fluorine partitioning in substantial amount between granitic melt and coexisting aqueous fluid phase and higher HF activity during the evolution of hydrothermal fluid. The mutual relationship of the fluorine minerals (topaz and fluorite) in the different alteration zones suggests an increase in the Ca2+ activity and decrease of H+ activity during the fluid evolution from greisenization towards alkali-metasomatised granite and the fluid is assumed to change from low to high activity ratio of Ca2+/H+.  相似文献   

14.
Some recent experiments on the determination of Au and the platinum-group elements (PGE) in geochemical samples are reviewed. Emphasis is given to the determination of ultra-low levels of PGE concentrations in resistant matrices, including chromites, molybdenites and ultrabasic ores. The problems and features of PGE determination in samples of various chemical composition are considered. For each sample type studied, a series of sample preparation techniques are proposed. These techniques included acid digestion, fusion with sodium peroxide, cold sintering with an oxidizing mixture of Na2O2+ Na2CO3 and also oxidizing fluorination with bromine trifluoride. A new approach for preparing geochemical material prior to digestion, based on mechano-chemical activation with simultaneous hyperfine grinding, is proposed and studied. The instrumental determination of PGE contents was carried out directly by AAS from extracted organic phases. It was found that a combination of digestion processes was required to achieve geochemical background levels of Au and PGE concentrations with the following detection limits: Pd, Rh - 1 ng g−1, Pt, Ru - 10 ng g−1, Au - 0.2 ng g−1, Ag - 0.1 ng g−1. The uncertainty in PGE and Au determination in geochemical samples is dependent on metal concentration, and also on their distribution in samples. The total analytical uncertainty of the proposed method is between 15-30%.  相似文献   

15.
Abstract: A strange, unidentified, Cu-Fe bearing zinc sulfide occurs in the Laloki massive sulfide deposit, Papua New Guinea. The mineral is optically uniform in texture but is chemically variable and zoned even within a single grain. Copper contents vary from 0.1 up to 8.85 wt%. Iron reaches 18.31 wt% at maximum and decreases as Cu increases. It is remarkable, however, that the total Fe+Cu remains essentially unchanged between roughly 18 and 20 wt%. Zn and S are least variable, giving 45.85–47.84 wt% and 33.48–34.58 wt%, respectively. Other trace elements such as Cd and Mn are in general less than 0.2 wt%. It is strongly suggested that the mineral in question constitutes a unique Fe-Cu substitutional solid solution series belonging essentially to the Zn–Fe–Cu–S system.
The ideal chemical formula of the solid solution series can well be presented as Zn10(Fe, Cu)5S15 or Zn2(Fe, Cu)S3, where Fe is always greater than Cu. It is intriguing that chalcopyrite blebs are recognizable restrictively only in nearby portions of the Cu-rich end member with the ideal composition close to Zn10Fe3Cu2S15. It has been confirmed by vacuum-sealed heating experiments that this mineral is decomposed to produce chalcopyrite and Fe-bearing normal sphalerite at temperatures below 200C. This would provide another evidence for the existence of such distinct phase as suggested here.  相似文献   

16.
Abstract: Major and rare earth element contents are reported for Late Archean banded iron formations (BIFs) in the Bababudan Group of the Dharwar Craton, South India. The BIFs are mostly composed of SiO2 (average1ρ = 54.88.1 wt%) and Fe2O3* (44.38.2 wt%). The Al2O3 and TiO2 contents are remarkably low, suggesting that detrital components were starved during the BIF deposition. The BIFs have a LREE-enriched pattern with a relatively high (La/Yb)N (6.644.07). Total REE concentrations (RE) vary from 5.2 to 65.3 ppm. The REE patterns are characterized by the presence of a very large negative Ce anomaly (Ce/Ce*: 0.13-0.83) and a positive Eu anomaly (Eu/Eu*: 0.96-2.45). The Eu/Eu* decreases and (La/Yb)N increases with a increase of RE. These correlations of REE indices are similar to those of modern hydrothermal iron-rich sediments near a mid-ocean ridge (MOR). Greenstones associated with the BIFs have MORB-like geochemical features. These geochemical and geological lines of evidence indicate that the depositional site of the BIFs was remote from a continent and/or island arc and that the BIFs were in situ hydrothermal sediments near a MOR. A striking negative Ce anomaly in the BIFs indicates that oxygenated deep-sea environments emerged at 2.9-2.7 Ga. The existence of contemporaneous Mn deposits in the Dharwar Craton supports this assertion. Our scenario of oxygen in the Earth's surface of the Late Archean is different from long-held notion that the atmosphere and ocean were persistently anoxic throughout the Archean.  相似文献   

17.
Oxygen isotope geothermometers for metamorphic rocks   总被引：10，自引：1，他引：10  
The Chicago mineral-carbonate oxygen isotope fractionation curves have been combined with mineral-water fractionation data for jadeite, zoisite and rutile and new data for grossular-water to provide a set of self-consistent mineral-pair calibrations. The A coefficients in the equation 1000 In α= A × 106T-2 of the new mineral-pair fractionations are
Jadeite Zoisite Grossular Rutile
Quartz 1.69 2.00 3.03 5.02
Jadeite 0.31 1.34 3.33
Zoisite 1.03 3.02
Grossular 1.99
The isotopic fractionation properties of natural pyralspite garnet [(Ca, Fe, Mg, Mn)3Al2Si3O12] can be approximated by those of the grossular end-member. Appropriate substitutions also yield coefficients for the solid-solution minerals: sodic pyroxene and epidote, e.g.
A quartz-sodic pyroxene= 2.75 - 1.06Xjd,
A quartz-epidote= 2.00 + 0.75Xps
where X Jd and X Ps are the mole fractions of the jadeite and pistacite components, respectively.
The new data set is particularly suitable for the geothermometry of metamorphic rocks. δ18O data from minerals of the high-pressure metamorphic rocks of the Sesia Zone of Italy and Cyclades Complex of Greece yield well-constrained mean temperatures of 572 and 478 C, respectively. Type III blueschist metabasalts of the Franciscan Formation of California give mean quartz-garnet temperatures of 354 C.  相似文献   

18.
We have developed a set of four synthetic standards for the rare earth and high field strength elements designed for use in the determination of those elements in silicates. The base material is a glass nominally at the eutectic of the MgO-Al2O3-SiO2 ternary system. The nominal doping level was 2 wt% of the elements as oxides. To avoid problems associated with peak interference, the elements were doped in four separate glasses.  相似文献   

19.
东天山阿拉塔格花岗岩体地球化学特征及其构造意义   总被引：2，自引：0，他引：2  
位于中天山地块南缘大黑山地区的阿拉塔格花岗岩体,岩性主要由花岗闪长岩、二长花岗岩、似斑状花岗岩组成,岩石具有高硅(w（SiO2）为66.29%~77.47%)、富碱(w（Na2O+K2O）为6.75%~9.93%)、高铝(w（Al2O3）为10.97%~14.40%)、低Sr(w（Sr）为（28.78~153.00）×10-6,平均为99.23×10-6)、低Ti（w（TiO2）为0.09％~0.77％）的特征。岩石的A/CNK值为1.19~1.50,为钙碱性过铝质岩石;岩石Eu亏损（δEu＝0.19~0.51）、LREE富集(LREE/HREE= 6.80~8.45,(La/Yb)N= 6.06~9.03),明显富集Rb、Th、K、Hf(Zr) 等大离子亲石元素(LILE),亏损Nb、Ta、P、Ti等高场强元素(HFSE);岩石的Ba含量较低,并具有明显的Sr负异常。结合区域地质特征,通过岩石的地球化学和Sr、Nd同位素综合分析,认为该花岗岩形成于后碰撞环境,且为壳幔混源的岩浆多期次侵位的复合岩体。  相似文献   

20.
Abstract A Hercynian charnockite occurs within high-grade gneisses in the Agly Massif, French Pyrenees. Its thermal history has been evaluated using the Fe-Mg distribution coefticient ( K D) between garnet and biotite. These minerals have different origins but similar compositions in the charnockites and host gneisses. In the charnockite, the Bi–Ga pairs are the retrograde products of Opx alteration. This Opx reaction with feldspar can be written. Opx + PI + Fluid 1(H2O + Al + K + Fe + Ti) = Bi + Ga + Q + Fluid 2(H2O + Na). The garnets are relatively Ca poor (4–2.5% grossular); they are automorphic and zoned in the gneisses and poikiloblastic in the charnockites. Both types show a retrograde rim (of few hundred microns'width) across which Fe and Mn increase as Mg decreases. The biotites show a good correlation between the octahedral cations (Ti4++ Fe2+) and (Mg2++ Al3+VI); Ti and Fe both increase, whereas Mg and AlVI decrease. There is an inverse linear correlation between Fe2+ and Mg2+ and the Fe/Mg ratio increases as Ti increases. The relation between Ti and K Ga-BiDFe-Mg is less clear: it seems that K D slightly decreases as Ti increases. The equilibration temperatures of Ga–Bi pairs are discussed: the charnockite Ga-Bi pairs have equilibrated between 550°C and 600°C; whereas those of the gneisses have equilibrated between 550°C and 650°C. Two main thermal steps appear: one in the gneisses between 600-650°C and a second one in both the gneisses and the charnockites between 550°C and 600°C.  相似文献   

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