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1.
M Santosh 《Journal of Earth System Science》1986,95(1):91-102
Major and trace element geochemistry of coexisting hornblendes and biotites from the Ambalavayal granite, northern Kerala, are presented. The hornblendes correspond to edenitic composition, whereas the biotites correspond to annite. The hornblendes typically show high Al2O3 contents (9·69–11·89%) comparable with those from anorogenic granites. The biotites are characteristically low Mg-type, similar to those reported from alkaline rocks. The distribution coefficients calculated for all the major and trace elements are presented and an evaluation of the nature of variation indicate near-chemical equilibrium conditions during the crystallization of the two minerals. The hornblende-biotite tie lines in the Fe3+?Fe2+?Mg compositional triangle, lie parallel to those of buffered biotites, indicating crystallization in an environment closed to oxygen and well above the Ni?NiO buffer. It is inferred that thefH2O increased towards the residual stage andfO2 values were high, in the range of 10?15 bars. 相似文献
2.
N.C.N. Stephenson 《Lithos》1979,12(2):73-87
Garnet-biotite (-cordierite) phase relations in high-grade gneisses of the south coast of Western Australia reflect at least two metamorphic episodes. Chemical uniformity of the interiors of garnet and cordierite grains suggest thorough equilibration during a major phase of metamorphism. Narrow Mg-depleted rims on garnet grain boundaries in contact with biotite or cordierite, and complementary Mg-enriched rims on contiguous cordierites are the result of subsequent retrograde re-equilibration. The absence of reaction zoning in biotites suggests more complete retrograde modification of this mineral.Comparison between granulite and amphibolite facies garnet-biotite pairs shows that Mn contents of both minerals are higher, and Ti contents of the biotites are lower, in the lower-grade rocks. These differences, although not entirely unrelated to grade, are more directly controlled by variations in host rock chemistry and modal amounts of garnet and biotite.Partitioning of Mg, Fe2+ and Mn between garnet and biotite is fairly uniform, with no clear differences between granulite and amphibolite facies pairs. Application of the Mg-Fe2+ distributions to the geothermometers devised by Perchuk, Thompson, and Goldman & Albee yields variable T estimates of 600–680°C, 580–780°C, and 475–715°C respectively, for the main metamorphism. These estimates are low compared with the T indicated for the granulite facies rocks by other evidence (i.e. > 750°C at 5 kb PT). The Mg-Fe2+ distributions between contiguous garnet-biotite rims suggest that retrograde re-equilibration occurred at least 20–140°C below the T of the main metamorphism. 相似文献
3.
Summary The chemical characteristics of coexisting biotites and hornblendes and host rocks are examined and discussed. The field data indicate that biotite derives from hornblende at decreasing metamorphism. A chemical equilibrium has been reached for Fe2+, Mg and Mn and approached, but not reached, for tetrahedral ions, Fe3+, Alvi and Ti. The disequilibrium is mainly dependent on biotite and is tentatively ascribed to the oxidizing conditions of the environment, at the time of biotite crystallization. The composition of biotite is thus partly related to that of hornblende and partly to the environment, while intracrystalline variations of hornblende are related to the chemical composition of the host rock and to varying metamorphic grade.
With 7 Figures 相似文献
Amphibole und Biotite der Hornblendegneise in einem Gebiet nordöstlich des Qagssit-Fjordes, Frederikshåb-Distrikt, Südwest-Grönland
Zusammenfassung Der Chemismus koexistierender Biotite und Hornblenden sowie von deren Muttergesteinen wird untersucht und diskutiert. Die Felddaten weisen darauf hin, daß der Biotit aus Hornblende bei abnehmender Metamorphose entsteht. Ein chemisches Gleichgewicht wurde für Fe2+, Mg und Mn erreicht; für die tetraedrisch koordinierten Ionen sowie Fe3+, Alvi und Ti fand eine Annäherung in seine Richtung statt, es wurde aber nicht erreicht. Das Ungleichgewicht hängt im wesentlichen mit dem Biotitgehalt zusammen, und es wird versuchsweise den Oxidationsbedingungen der Umgebung bei der Biotitkristallisation zugeschrieben. Die Zusammensetzung des Biotits hängt folglich teilweise mit jener der Hornblende und teilweise mit der Umgebung zusammen, während die intrakristallinen Variationen der Hornblende von der chemischen Zusammensetzung des Muttergesteins und dem variierenden Metamorphosegrad abhängen.
With 7 Figures 相似文献
4.
《International Geology Review》2012,54(6):681-690
On the basis of 135 pairs of chemical analyses of coexisting hornblendes and biotites, we have established a relationship between the contents of AlIV, AlVI, Fe3+, Mg, Ti, Na, and K and the overall iron index in the hornblendes and the depth of granitoid formation. This relationship has been emphasized by the R-method of factor analysis. We have examined the strength and nature of the correlations between the elements in the hornblendes and have considered the types of Isomorphism in the amphiboles according to depth, from the viewpoint of crystal chemistry. A regular increase in the amounts of AIV in hornblende from <0.8 to > 1.6 formula units; of (AlVI + Fe3+ + Ti) from <0.5 to >1. 0 formula units; of (K + Na) from <0.35 to >0. 64 formula units; and of Group A from <0.24 to >0.51 formula units has been recorded from the near-surface granitoids to the ultra-abyssal types. Biotites In this respect display no adequately clear and reliable information.—Authors. 相似文献
5.
J. P. Bard 《Contributions to Mineralogy and Petrology》1970,28(2):117-134
This paper attempts to illustrate the chemical variations of metamorphic hornblendes regarding host rocks and prograde variations. Changes related to bulk chemistry (orthoamphibolites) mainly concern Si, Al, Mg, Fetot and Ca. The Mg, Fe2+ and Fe3+ contents of hornblendes are, however, not strictly related to host rook compositions and Mg enrichments are correlated with increasing Fe3+ contents in the amphiboles. Thus, variations of oxygen fugacity may control the Mg contents of the Ca amphiboles studied but this does not show clear relations with the prograde metamorphism. The most sensitive but irregular variation related to the metamorphic conditions is the prograde enrichment of the alkalis into the A vacant position and an increase of the (Na+K)tot/Na+K+Ca ratios of the amphiboles. Increasing Ti and AlIV contents as well as decreasing AlVI concentrations are also, but much less evidently, related to increasing T and P. A variation trend from tschermakitic to edenitic hornblendes may be drawn using Shido's end members calculation; this tendency and the relative deficiency of AlVI contents in the low-grade members suggests that the amphiboles studied were subjected to conditions of a low-pressure metamorphism type. Such a conclusion is in agreement with the occurrence of andalusite-cordierite/sillimanite-cordierite associations in the metapelitic rocks, and the absence of Fe-rich garnet and epidote from the orthoamphibolites of the amphibolite facies at Aracena. Comparisons with Ca amphiboles from other metamorphic areas show, in agreement with various authors, that Abukuma hornblendes are similar to those encountered in high-grade thermal aureoles and tonalitic intrusives but different from the hornblendes of Barrovian metamorphism types. 相似文献
6.
Complete chemical analyses, structural formulae and trace elementdata are presented for 9 hornblendes and 12 biotites from thecharnockitic and associated rock types of Kondapalli (AndhraPradesh, India), some 200 miles north of the type area nearMadras. The chemical characteristics of the hornblendes are:very high [Al]4, nearly constant Ca, very high and nearly constanttotal alkalis (Na2O > K2O in the hornblendes of ultrabasiccharnockites and Na2O < K2O in those of basic charnockites),very high F and Cl, low total water, and Ni in amount greaterthan Co. The biotites are characterized by high Ti and F, lowMn, total absence of Ca, exceptionally high amounts of Cl, lowtotal water, and have Ni > Co; the biotites from differentgroups of host rocks have different Al and Fe3+ contents. Thevariations in composition of these minerals are interpretedas due to the change in bulk rock chemistry and mineralogy andnot to the change in temperatures of crystallization. The element distributional relationships in hornblende-biotite,hornblende-orthopyroxene, hornblende-clinopyroxene, biotite-orthopyroxene,and biotite-clinopyroxene pairs from the Kondapalli charnockitesare evaluated, with particular attention to the partition ofFe2+, Mg, Mn, Ti, Cr, Ni, Co, and V, and comparisons are madewith similar data available for corresponding mineral pairs.Highly consistent and uniform distribution coefficients forFe2+ and Mg (and a small range of distribution coefficientsfor many of the trace elements) are obtained for most of thedifferent sets of mineral pairs from Kondapalli, suggestingthat equilibrium distribution of the elements between the phaseshad been attained. 相似文献
7.
用置换矢量概念解释了115个天然 Fe-Li 云母化学成分的变化。Fe-Li 云母是三八面体 Li-Fe-Al 云母,其基本置换是四锂云母置换。由于 Al-Li 白云母置换和白云母置换的影响,其化学组成变化的基本趋势呈明显的非线性,因而 Fe-Li 云母不是真正的二元系。作为 Fe-Li 云母,富铁黑云母和铁叶云母都是最富铁的成员,因而建议称 Fe-Li 云母为黑云母-锂云母系列。根据化学成分,晶胞参数和折光率的异常变化还提出了该系列自然分类的方案。 相似文献
8.
河北矾山杂岩体中单斜辉石的研究 总被引：3，自引：1，他引：2
河北矾山杂岩体属于二氧化硅不饱和的超钾质碱性-过碱性岩浆系列,由单斜辉石岩、辉石正长岩和碱长正长岩等不同类型岩石组成。各类型岩石主要组成矿物为单斜辉石、黑云母、石榴石和正长石。本文利用电子探针对单斜辉石进行了详细研究,发现所有单斜辉石属于高钙透辉石,随着岩浆的演化,主要表现为Fe2+对Mg2+的替代关系,结晶趋势为透辉石→钙铁辉石,这揭示矾山杂岩体岩浆体系的特点是高温、中等大小的氧逸度、贫硅、富碱（尤其是钾）。辉石中的AlIV含量取决于岩浆的硅饱和度,硅越不饱和,AlIV含量越高;AlVI含量则与体系中的Al含量呈正相关关系。由Al对Si的替代引起的电荷不平衡主要由八面体位置的Fe3+来补偿,其次为少量的Ti4+和更少量的Al3+。体系中的Ti含量与体系的温度呈正相关关系,而Na含量则与辉石中的Ti和Fe3+含量成正相关关系。不同类型岩石中单斜辉石从核部到边部随着Mg#的降低,Al、Ti含量呈现不同的演化趋势,这是因为它们于岩浆演化的不同阶段开始结晶,经历了不同的岩浆演化史。碱性岩中高钙辉石的出现和成分环带的普遍发育是由岩浆的贫硅富钾特征决定的。单斜辉石的成分不仅受控于结晶时的温度、压力条件,也受控于岩浆的总成分及其变异。 相似文献
9.
赣杭构造带灵山花岗岩体黑云母的矿物化学特征及其对岩石成因的指示意义 总被引：1，自引：0，他引：1
灵山花岗岩体在平面上为一环状分布的侵入体,中心为角闪石黑云母花岗岩,外围为黑云母花岗岩。在角闪石黑云母花岗岩中分布有大量的暗色镁铁质微粒包体。黑云母是大多数中酸性火成岩中比较重要的一种镁铁质矿物,它能很好地反映寄主岩浆的属性和成岩时的物理、化学条件,因此,本文对这两种花岗岩及镁铁质微粒包体中的黑云母开展了系统的岩相学观察和电子探针化学组成研究,探讨灵山岩体的物质来源、成岩条件和岩浆的混合作用过程。研究结果表明两种花岗岩体的黑云母具有不同化学成分,而暗色镁铁质微粒包体中黑云母的化学成分则变化较大。三种黑云母均在低氧逸度条件下晶出。两种花岗岩中的黑云母均富Fe贫Mg,属于铁质黑云母,含铁系数[(Fe~(3+)+Fe~(2+))/(Fe~(3+)+Fe~(2+)+Mg~(2+))]分别为0.65~0.70,0.72~0.78,FeOT/MgO均接近7.04。MF值[2×Mg/(Fe~(2+)+Mg+Mn)]分别为0.64~0.76和0.48~0.60,指示两种花岗岩的物质来源都是以壳源为主。镁铁质微粒包体中黑云母的MF值变化范围比较大,为0.63~1.06,为铁质黑云母到镁质黑云母,暗示包体岩浆经历过不同程度的岩浆混合作用。镁铁质微粒包体中部分黑云母与角闪石黑云母花岗岩中黑云母的结晶条件相似,而部分则有明显差异,推测是由于基性的镁铁质包体岩浆注入到酸性的花岗岩浆是一个连续多阶段的过程。 相似文献
10.
Discovery and Genetic Mechanism of Basic Granulite in the Altay Orogenic Belt, Xinjiang, NW China 总被引：1，自引：0，他引：1
LI Zilong CHEN Hanlin YANG Shufeng DONG Chuanwan XIAO Wenjiao LI Jiliang YE Ying WANG JianDepartment of Earth Sciences Faculty of Science Zhejiang University Hangzhou Institute of Geology Geophysics Chinese Academy of Sciences Beijing 《《地质学报》英文版》2004,78(1):177-185
Altay granulite (AG), which represents the product of high-grade metamorphism in the lower crust, was newly found in the Wuqiagou area, Fuyun County in the Altay orogenic belt, Northwest China. It is composed mainly of hypersthene, augite, basic plagioclase, amphibole and brown biotite. Its mineral compositions of amphibole and biotite are rich in Mg/(Mg+Fe2+) and Ti. Geochemically, the AG is enriched in Mg/(Mg+Fe2+) and A12O3, and poor in CaO, with depletion of U, Th, K and Rb contents. Furthermore, geochemical data reflect that the protolith of the AG is igneous-genetic calc-alkaline basalt formed under an island arc environment. The AG has ZREE of 92.38-96.58 ppm and enriched LREE model with weak positive Eu anomaly of 1.09-1.15. In the MORB normalized spider diagram, the AG shows tri-doming pattern with a strong negative Nb anomaly and medium negative P and Ti anomalies, reflecting that the AG has tectonic relation with subduction or subduction-related materials. The P-T conditions of peak metamorphi 相似文献
11.
湘南宝山矿床花岗闪长斑岩中黑云母的矿物学特征及其指示意义 总被引：8，自引：2，他引：6
湖南宝山矿床处于坪宝矿带的北端,是湘南地区最大的铜多金属矿床。为了进一步探讨矿区内花岗质岩石的形成条件及成矿潜力,文章在详细的野外地质和岩相学观察的基础上,对与成矿密切相关的花岗闪长斑岩中的黑云母进行了详细的矿物化学分析。电子探针分析结果表明:宝山花岗闪长斑岩中的黑云母为铁质黑云母和镁质黑云母,其中,Ti介于0.18~0.30,且Mg/(Mg+Fe2+)值介于0.42~0.58,属于典型的岩浆成因黑云母;黑云母的氧化系数为0.16~0.26,w(Mg O)为8.17%~11.72%,平均9.3%,MF值范围为0.38~0.50,指示其岩体属于壳幔混源型的I型花岗岩;岩体中以黑云母的全铝含量计算的结晶压力为97~174 MPa,相应的结晶深度为3.67~6.57 km,平均深度为5.12 km。其log f(O2)变化范围为-14.5~-12.8,表明黑云母是在较高氧逸度条件下结晶形成的,有利于铜矿的形成。 相似文献
12.
RALPH KRETZ 《Journal of Metamorphic Geology》1990,8(5):493-506
Garnet-biotite gneisses, some of which contain sillimanite or hornblende, are widespread within the Otter Lake terrain, a portion of the Grenville Province of the Canadian Shield. The metamorphic grade is upper amphibolite to, locally, lower granulite facies. The atomic ratio Fe2+/(Fe2++ Fe3+) in biotite ranges from 0.79 to 0.89 (ferrous iron determinations in 10 highly pure separates), with a mean of 0.86. Mg and Fe2+ atoms occupy 67–78% of the octahedral sites, the remainder are occupied by Fe3+, Ti, and Al, and some are vacant. Mg/(Mg + Fe2+), denoted X, in the analysed samples ranges from 0.32 to 0.65. Garnet contains 1–24% grossular, 1–12% spessartine and X ranges from 0.07 to 0.34. Compositional variation in biotite and garnet is examined in relation to three mineral equilibria: (I) biotite + sillimanite + quartz = garnet + K-feldspar + H2O; (II) pyrope + annite = almandine + phlogopite; (III) anorthite = grossular + sillimanite + quartz. Measurements of X (biotite) and X (garnet) are used to construct an illustrative model for equilibrium (I) which relates the observed variation in X to a temperature range of 70°C or a range in H2O activity of 0.6; the latter interpretation is preferred. In sillimanite-free gneisses, the distribution of Mg and Fe2+ between garnet (low in Ca and Mn) and biotite is adequately described by a distribution coefficient (KD) of 4.1 (equilibrium II). The observed increase in the distribution coefficient with increasing Ca in garnet is ln KD= 1.3 + 2.5 × 10?2 [Ca] where [Ca] = 100 Ca/(Mg + Fe2++ Mn + Ca). The distribution coefficient is apparently unaffected by the presence of up to 12% spessartine in garnet. In several specimens of garnet-sillimanite-plagioclase gneiss, the Ca contents of garnet and of plagioclase increase in unison, as required by equilibrium (III). The mean pressure calculated from these data (n= 17) is 5.9 kbar, and the 95% confidence limits are ±0.5 kbar. 相似文献
13.
A. I. Okay 《Contributions to Mineralogy and Petrology》1980,72(3):243-255
Glaucophane-lawsonite facies blueschists representing a metamorphosed sequence of basic igneous rocks, cherts and shales have been investigated northeast of the district of Tav?anli in Northwest Turkey. Sodic amphiboles are rich in magnesium reflecting the generally high oxidation states of the blueschists. Lawsonite has a very uniform composition with up to 2.5 wt.% Fe2O3. Sodic pyroxenes show an extensive range of compositions with all the end-members represented. Chlorites are uniform in their Al/(Al+Fe+Mg) ratio but show variable Fe/ (Fe+Mg) ratios. Garnets from metacherts are rich in spessartine (>50%) whereas those from metabasites are largely almandine. Pistacite rich epidote is found in metacherts coexisting with lawsonite. Phengites are distinctly higher in their Fe, Mg and Si contents than those from greenschist facies. Hematites with low TiO2 are ubiquitous in metacherts. Fe2+/Mg partitioning between chlorite and sodic amphibole is strongly controlled by the calcium content of the sodic amphibole and ranges from 1.1 for low calcium substitution to 0.8 for higher calcium substitution. The Al/Fe3+ partition coefficient between sodic amphibole and sodic pyroxene is 2.1. A model system has been constructed involving projections from lawsonite, iron-oxide and quartz onto a tetrahedron with Na, Al, Fe2+ and Mg at its apices. Calcite is treated as an indifferent phase. The model system illustrates the incompatibility of the sodic pyroxene with chlorite in the glaucophanelawsonite facies; this assemblage is represented by sodic amphibole. Sodic amphibole compositions are plotted in terms of coexisting ferromagnesian minerals. Five major areas on the sodic amphibole compositional field are delineated, each associated with one of the following minerals: chlorite, stilpnomelane, talc, almandine, deerite. 相似文献
14.
Experiments from 640 to 680?°C, 200 MPa H2O at?f O2?≈?NNO, employing a natural?F-rich?vitrophyric rhyolite from Spor Mountain, Utah, assessed the effect of variable Mg′ [100Mg/(Mg?+?Mn?+?Fe)] on the partitioning of fluorine and chlorine between biotite (Bt) and melt. Over this temperature interval, Bt (?±?fluorite, ?±?quartz) is the sole liquidus phase. Partition coefficients for fluorine between biotite and glass (DF Bt/melt) show a strong dependence on the Mg′ of Bt.?DF Bt/melt varies from???1.5 to 7.2 over the range of Mg′ from 21 to 76. A strong linear correlation between?DF Bt/melt?and Mg′ has a slope of 9.4 and extrapolates through the origin (i.e., DF Bt/melt?≈?0 at Mg′?=?0, an annite-siderophyllite solid solution in these experiments). DCl Bt/melt values (???1 to 6) in the same experiments vary inversely with Mg′. The Al-content of biotite does not vary with the aluminum saturation index (ASI?=?molar Al2O3/Σ alkali and alkaline earth oxides) of melt, but two exchange mechanisms involving Al appear to operate in these micas: (1) Alvi?+?Aliv?? Siiv?+?Mgiv, and Mgiv?+?2Aliv? 2Siiv?+?□iv. The effects of other components such as Li or other intensive parameters including f O2 have yet to be evaluated?systematically. At comparable Mg′ of Bt, however, the Spor Mountain rhyolite yields higher DF Bt/melt values than an Li-rich, strongly peraluminous melt previously investigated. The results indicate that the Mg′ of Bt exerts the principal control on halogen partitioning, with ASI and T as second-order variables. The experimental partition coefficients compare well with other experimental results but not with most volcanic rocks. Magmatic Bt from most rhyolites records higher DF Bt/melt due to reequilibration with degassed (H2O-depleted) magma and perhaps with F2O?1 exchange that may accompany oxidation ([Fe3+O] [Fe2+OH]?1). This behavior is evident in magmatic biotite from a zoned peraluminous rhyolite complex near Morococala, Bolivia: Bt is sharply zoned with F-rich rims, but Bt(core)-melt inclusion pairs fall on our experimental curve for DF Bt/melt. These experimental data can be used in part to assess the preservation of magmatic volatile contents in plutonic or volcanic silicic rocks. For plutonic rocks, the actual F-content of melt, not a relative activity ratio involving HF species, can be reasonably estimated if the mica has not undergone subsolidus reequilibration. This information is potentially useful for some shallow-level Ca-poor magmas that are thought to be rich in F (e.g., A- and S-type granites) but do not conserve F well as rocks. 相似文献
15.
Structural formulae of many Ti-rich hornblendes and biotites exhibit cation deficiencies that increase with Ti content. These deficiencies may be caused by the presence of trivalent instead of tetravalent Ti, of oxygen replacing hydroxyl, or of vacancies on octahedral cation sites. In order to determine the oxidation state of their Ti, electron energy-loss spectra of natural, Ti-rich hornblende and biotites are compared with spectra of natural and synthetic Ti-bearing oxides and silicates. Spectra of Ti2O3 and TiO2 demonstrate that the Ti L 2,3 edge for Ti3+ is shifted by ca. 2 eV to lower energy relative to the edge for Ti4+. Oxidation states of Ti determined by energy-loss spectroscopy for several minerals agree with data from other techniques: tetravalent for Ti-omphacite, perovskite, ilmenite and titanite; trivalent for NaTi3+Si2O6 pyroxene and fassaite from the Allende meteorite. The energy-loss spectra of the hornblende and biotite show that their Ti is tetravalent and cannot be the cause of the cation deficiencies. The relations between Ti contents and the number of deficiencies differ for hornblende and biotite. Hornblende shows a 2:1 relation between Ti content and deficiencies, suggesting Ti is coupled to an oxygen that is replacing hydroxyl (Ti-oxyhornblende substitution). Biotite shows a 1:1 relation, consistent with coupling of Ti to a vacant octahedral cation site (Ti-vacancy substitution) or to a variable combination of such vacancies and two oxygens replacing hydroxyls (Ti-oxybiotite substitution). 相似文献
16.
Suzanne Y. Wass 《Lithos》1979,12(2):115-132
Geochemical and textural data on clinopyroxenes in individual alkali basaltic flows from provinces in eastern Australia and the Massif Central can be used to differentiate four different modes of origin (three at high pressure) for these clinopyroxenes. Many single flows from the two provinces contain clinopyroxenes of three, or even four, of these origins. Rare flows contain core clinopyroxene with overgrowths of clinopyroxenes of two distinct generation. Each of the overgrowth is compositionally analogous to clinopyroxenes occurring in xenoliths or as discrete crystals in the same host lava. Such rimming relationships provide evidence that the host magma has undergone high pressure crystallisation and confirm that some xenoliths and megacrysts are cognate. With decreasing pressure the major changes in clinopyroxene chemistry are an increase in the ratio Allv/Alvi, a linear increase of atomic proportions of Ti and Al with decreasing Si, and an increase in the Ti: (100 Mg/(Mg + Σ Fe)) ratio of the pyroxenes. Al2O2 wt, % is an unreliable potential geobarometric indicator; consideration of tetrahedral and octahedral site occupancies by Al (Allv/Alvl ratio) is necessary. High-pressure fractionation dominated by clinopyroxene is postulated for some basaltic-composition, resulting in SiO2 depletion, alkali enrichment and decrease in the Mg/(Mg + Fe2+) value of the host magma. 相似文献
17.
G. E. Eleftheriadis 《Mineralogy and Petrology》1988,38(2):117-126
Summary In the zoned clinopyroxene phenocrysts from the volcanic rocks of Almopia the Mg/Fe ratio and the contents of Mn, and mostly of Na, increase from the core towards the rim of the crystals, whereas the Fe3+/Fe2+ ratio, and in many cases the contents of Ca, decrease. On the contrary, the content of Si decreases from inside outwards or remains almost constant whereas Al and Ti increase.The high Ca-content of the clinopyroxenes, low Ti, and limited Fe-enrichment, with a trend from Ca43.3: Mg47.0: (Fe + Mn)9.7 to Ca46.6: Mg42.2: (Fe + Mn)11.2, illustrate the shoshonitic to cale-alkaline nature of the parental magma.The composition of the clinopyroxenes indicates that, of all possible controlling factors, the high water-vapour pressure is considered to play an important role for the AlIV fluctuations during the crystallization.
Zonierte klinopyroxene der vulkanite von almopia (Voras-Gebirge), Zentral-Mazedonien, Griechenland
Zusammenfassung Bei den zonierten Klinopyroxeneinsprenglingen der Vulkanite von Almopia nehmen das Mg/Fe-Verhältnis und die Gehalte an Mn und meistens an Na in den einzelnen Zonen vom Kern zum Rand zu, während das Fe3+/Fe2+-Verhältnis, und in vielen Fällen die Gehalte an Ca, abnehmen. Im Gegensatz dazu nimmt der Gehalt an Si von innen nach außen ab oder bleibt fast konstant, während Al und Ti zunehmen.Der hohe Ca-Gehalt und gleichzeitig niedrige Ti-Gehalt der Klinopyroxene, zusammen mit ihrer begrenzten Fe-Anreicherung und einem Trend von Ca43.3: Mg47.0: (Fe + Mn)9.7 bis Ca46.6: Mg42.2: (Fe + Mn)11.2 weisen auf die shoshonitische bis kalk-alkalische Natur des Stammagmas hin. Die Zusammensetzung der Klinopyroxene weist darauf hin, daß der hohe Wasserdampfdruck im Magma auch eine wichtige Rolle für Schwankungen im AlIV-Gehalt während der Kristallisation darstellt.相似文献
18.
The effect of whole-rock MnO content on the stability of garnet in pelitic schists during metamorphism 总被引：6，自引：1，他引：6
Garnet-bearing mineral assemblages are commonly observed in pelitic schists regionally metamorphosed to upper greenschist and amphibolite facies conditions. Modelling of thermodynamic data for minerals in the system Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O, however, predicts that garnet should be observed only in rocks of a narrow range of very high Fe/Mg bulk compositions. Traditionally, the nearly ubiquitous presence of garnet in medium- to high-grade pelitic schists is attributed qualitatively to the stabilizing effect of MnO, based on the observed strong partitioning of MnO into garnet relative to other minerals. In order to quantify the dependence of garnet stability on whole-rock MnO content, we have calculated mineral stabilities for pelitic rocks in the system MnO–Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O for a moderate range of MnO contents from a set of non-linear equations that specify mass balance and chemical equilibrium among minerals and fluid. The model pelitic system includes quartz, muscovite. albite, pyrophyllite, chlorite, chloritoid, biotite, garnet, staurolite, cordierite, andalusite, kyanite. sillimanite, K-feldspar and H2O fluid. In the MnO-free system, garnet is restricted to high Fe/Mg bulk compositions, and commonly observed mineral assemblages such as garnet–chlorite and garnet–kyanite are not predicted at any pressure and temperature. In bulk compositions with XMn= Mn/(Fe + Mg + Mn) > 0.01, however, the predicted garnet-bearing mineral assemblages are the same as the sequence of prograde mineral assemblages typically observed in regional metamorphic terranes. Temperatures predicted for the first appearance of garnet in model pelitic schist are also strongly dependent on whole-rock MnO content. The small MnO contents of normal pelitic schists (XMn= 0.01–0.04) are both sufficient and necessary to account for the observed stability of garnet. 相似文献
19.
Kåre Kullerud 《Contributions to Mineralogy and Petrology》1995,120(1):42-59
Barium-, Cl- and Ti-rich biotite occurs together with garnet, plagioclase and amphibole within narrow shear zones in 1800 Ma old noritic granulites in the Flakstadøy Basic Complex, Lofoten, north Norway. The granulite facies assemblage, plagioclase, clinopyroxene, orthopyroxene, biotite and ilmenite, was replaced by an amphibolite facies mineral assemblage including Ba-, Cl- and Ti-rich biotite during ductile deformation. Biotite shows complex compositional variations with respect to the contents of Ba, K, Cl, Ti, Al, Fe, Mg and Si. There are correlations between Si, AlIV, K, Ba and Cl and between AlVI and Ti. Titanium and Cl are uncorrelated. The Fe and Mg are correlated to both Cl and Ti. Multivariate analysis shows that most of the compositional variation of biotite can be described by two exchange reactions. This indicates that most of the variation in biotite composition was controlled by two chemical variables of the system. The content of the first exchange component (Ti1.0 Fe0.6 Al
-1.1
VI
Mg-0.8) in biotite can be related to the original distribution of Ti-bearing minerals in the igneous protolith. The content of the second exchange component (Al
0.4
IV
Fe0.8 Ba0.5 Cl1.0 Si-0.4 Mg-1.0 K-0.5 OH-1.0) is related to compositional variations of an externally derived Ba- and Cl-bearing fluid in equilibrium with biotite.The initially low Cl-content of the externally derived fluid was increasing during bioite forming reactions, because OH was preferentially incorporated, relative to Cl, into biotite. Continued hydration/chloridisation reactions resulted in a gradual consumption of the free fluid phase, resulting in local fluid-absent conditions. The composition of biotite reflects the composition of the last fluid in equilibrium with the mineral, i.e. the composition of the fluid immediately before the grain boundaries were fluid-undersaturated. Thus, the variations in biotite composition reflect how the fluid was gradually consumed throughout the shear zone rock. The correlations between Fe, Mg, Ba, K and Cl can be attributed to differences between the structure of the crystal lattices and the sizes of the cation sites of OH-phlogopite and Cl-annite. The dependency of the Fe/Mg ratios of biotite on the Cl-and Ti-content has a strong effect on the Fe–Mg partitioning between biotite and garnet. The relationship between lnKD, X
Ti
Bt
and X
Cl
Bt
can be expressed by the regression equation: lnK
D
=-1.82+2.60X
Ti
Bt
+5.67X
Cl
Bt 相似文献
20.
Chemial analyses of twelve amphiboles from the area around Terakanambi are presented. Results indicate that they are ferro-hornblende
and ferro-pargasitic hornblende types in banded iron formations; magnesio hornblende in ultramafic rocks and edenite; and
ferroan pargasite and ferroan pargasitic hornblende types in calcamphibolites. Titanium content in the amphiboles of the present
study is relatively low compared to results from similar zones elsewhere. The lower titanium content of the amphiboles may
be attributed to either bulk chemical composition or to low oxygen fugacity. Mg/Fe ratios vary considerably and it is mainly
controlled by host rock composition. The plots of calcic amphiboles on (lOONa/Ca + Na)/(100 Al/Si + Al) and Aliv/Alvi diagrams indicate that they are of medium to low pressure type. 相似文献