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1.
Ninety-seven mineral phases consisting of ten chloritoids, fifteen epidotes, sixteen garnets, four sphenes, seven rutiles, seven pyroxenes, thirteen blue amphiboles, two green amphiboles, eleven phengites, two paragonites, a mariposite, seven chlorites, and two specimens of albite were obtained from the metamorphic rocks of Île de Groix, and their chemical, physical, optical and X-ray properties determined. The chloritoids are all optically positive, monoclinic polymorphs with large 2V, moderate refractive indices and characterized by high densities. Their fluorine contents have been used to propose a new upper limit for OHF substitution in the chloritoid structure, suggesting that partial pressure of fluorine might modify the stability of chloritoids from that determined in pure H2O. The epidotes belong to the Al-Fe epidote series and are epidote sensu stricto. The almandine-rich garnets and the chloromelanites are metastable relics in the glaucophane schists. The grossular contents of the calcareous schist garnets are believed to have become depressed under high CO2 pressure and the low Tschermak's contents of the pyroxenes are to be explained by equilibria involving epidote at high and low temperature when the Tschermak's components will break down to epidote group minerals. The sphenes contain appreciable amounts of combined water, fluorine substituting for oxygen and aluminium substituting for silicon and titanium. The presence of H3O+ is suspected in a specimen of blue amphibole. The barroisite has a composition between glaucophane and hornblende. On account of its high Fe3+ content it is believed to have formed under higher P O 2 than the blue amphiboles. The paragonites which occur in the ohloritoid veins are unstable in the potassium-rich aluminous schists. The phengites show a tendency towards sericitic composition due to post-glaucophanisation readjustments under the lower pressure conditions of the greenschist facies. Some of the Fe3+ contents of the chlorites are interpreted as due to oxidation of ferrous iron, e.g. 2 [Fe(OH)2]2FeOOH + H2. The minerals show strong chemical control of the host rock and their Mn contents are directly related to those of the minerals from which they have evolved through retrogression.Chloritoids and epidotes that are not associated with garnets contain higher amounts of manganese; similarly, the two blue amphiboles with the highest FeMg ratios were obtained from rocks in which garnet has not appeared. It is therefore believed that ottrelite and piemontite would be stable only at the lowest subfacies of the greenschist facies. Also, the ironrich amphiboles must have evolved from low-grade iron-aluminium chlorites, since on the appearance of garnet in a schist iron-aluminium chlorites react with quartz to give almandine and Mg-rich chlorites. The Fe2+Mg ratios of the blue amphiboles therefore reflect the grade of the original schist in which the minerals formed.  相似文献   

2.
Several petrologic experiments have demonstrated that in igneous and metamorphic reactions amphibole minerals can break down by a subsolidus dehydration reaction, but evidence for the reaction in natural rocks has been lacking. Evidence for the breakdown of an edenite-pargasite amphibole by a subsolidus dehydration reaction has now been found in an andesite flow from Garner Mountain, southern Cascase Range. The andesite contains one modal percent of crystal clots formed of crystallites of opx, cpx, plag, K-spar, opaque and quartz. The crystal clots retain the original amphibole morphology and intra-clot pyroxenes are aligned with crystallographic c parallel to c in the amphibole precursor; these conditions would not be duplicated by a melting reaction.Microprobe analyses of the bulk clot and the intra-clot minerals suggest the solid-state reaction: 100 amph+10 SiO2=>55 cpx+33 plag+22 opx+ 1 opq+1 ksparPyroxene thermometry of the andesite groundmass pyroxenes and the intra-clot pyroxenes demonstrates that the amphibole dehydration reaction occurred in the xenocrystic amphiboles as a result of heating by the near-solidus andesite magma.  相似文献   

3.
Ca- and Na-rich pyroxene-amphibole compositions and textures from a range of felsic alkaline rocks have been studied in detail. The data indicate that in a single sample, when amphibole crystallizes, a gap is observed between Ca- and Na-rich pyroxene compositions. This break in composition is analogous to Aoki's (1964) immiscibility gap between Ca-and Na-rich pyroxenes and can be overlooked when considering pyroxene compositions from a suite of rocks. The role of volatiles in governing the stability and composition of amphiboles is discussed. The presence of late crystallizing Na-rich pyroxene is related to the development of peralkinity in the late-stage melts.On extrusion, many alkaline rocks lose their volatiles and amphibole is absent. In these rocks complete zoning from Ca-rich to Na-rich pyroxene compositions are observed within the one sample.  相似文献   

4.
The paper discusses the petrography, mineralogy, petrochemical affinities, P/T crystallization regimes and genetic aspects of four garnet clinopyroxenite inclusions from diatremes in the Gloucester area, New South Wales. Inclusion mineral assemblages (which generally display textural evidence of annealing) include garnet-plagioclase-(sulphur-rich scapolite)-clinopyroxene, garnet-hornblende-orthopyroxene-clinopyroxene and garnet-hornblende-clinopyroxene. The garnet-plagioclase clinopyroxenite inclusion possesses an essentially alkali basaltic chemistry. It probably represents a crystallized basaltic liquid whereas the petrochemical affinities of the two garnet pyroxenites carrying amphiboles are more appropriate to subcalcie clinopyroxenites with variable Mg/Fe ratios. Experimental and other data suggest that the Gloucester garnet clinopyroxenite suite crystallized at pressures of the order of 10–14 kb and temperatures in the vicinity of 1000° C. The chemical compositions of many garnet pyroxenites, occurring either as inclusions in alkali basaltic rocks or as localized facies within some alpine-type peridotites, such as those in the western Mediterranean region, suggest that they can be interpreted as lower temperature heteromorphs of “primitive” subcalcic clinopyroxenites, variable in Al contents and hy/di ratios, but retaining consistently low Ti, Na, K and P. It is suggested that many inclusions of garnet (-spinel) pyroxenite and subcalcie Clinopyroxenite, restricted to alkali basaltic rocks and their associates, originally may have been interleaved with upper mantle aluminous peridotites and that they represent partial melt products of their aluminous peridotitic hosts.  相似文献   

5.
The Wadi Dabr intrusive complex, west of Mersa-Alam, Eastern Desert, Egypt ranges in composition from gabbro to diorite, quartz diorite and tonalite. The gabbroic rocks include pyroxene-horn blend e gabbro, hornblende gabbro, quartz-hornblende gabbro, metagabbro and amphibolite. Mineral chemistry data for the gabbroic rocks indicate that the composition of clinopyroxenes ranges from diopside to augite and the corresponding magma is equivalent to a volcanic-arc basalt. Plagioclase cores range from An75 to An34 for the gabbroic varieties, except for the metagabbro which has An 11–18. The brown amphiboles are primary phases and classified as calcic amphiboles, which range from tschermakitic hornblende to magnesiohornblende. Green hornblende and actinolite are secondary phases. Hornblende barometry and hornblende-plagioclase themometry for the gabbroic rocks estimate crystallisation conditions of 2–5 kb and 885–716°C.The intrusive rocks cover an extensive silica range (47.86–72.54 wt%) and do not exhibit simple straight-line variation on Harker diagrams for many elements (e.g. TiO2, Al2O3, FeO*, MgP, CaO, P2O5, Cr, Ni, V, Sr, Zr and Y). Most of these elements exhibit two geochemical trends suggesting two magma sources.The gabbroic rocks are relatively enriched in large ion lithophile elements (K, Rb, Sr and Ba) and depleted in high field strength elements (Nb, Zr, Ti and Y) which suggest subduction-related magma. Rare earth element (REE) data demonstrate that the gabbroic rocks have a slight enrichment of light REE [(La/Yb)N=2.67−3.91] and depletion of heavy REE ((Tb/Yb)N=1.42−1.47], which suggest the parent magma was of relatively primitive mantle source.The diorites and tonalites are clearly calc-alkaline and have negative anomalies of Nb, Zr, and Y which also suggest subduction-related magma. They are related to continental trondhjemites in terms of Rb---Sr, K---Na---Ca, and to volcanic-arc granites in terms of Rb---and Nb---Y.The Wadi Dabr intrusive complex is analogous to intrusions emplaced in immature ensimatic island-arcs and represents a mixture of mantle (gabbroic rocks) and crustal fusion products (diorites and tonalites) modified by fractional processes.  相似文献   

6.
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   

7.
Experimental studies of the incorporation of chlorine in trioctahedral biotite-like micas, belonging to the series phlogopite-annite, phlogopite-KCo3AlSi3O10(OH)2 and phlogopite-KNi3AlSi3O10(OH)2, were performed at 600°C and 2 kbars, with a duration of two weeks.The results confirm for the incorporation of an anion in a crystal structure, the fundamental role of the dimension of the anion site, as has been established for cations in previous works. In biotites, the dimension of (OH-Cl) site is mainly controlled by the rotation angle α of the tetrahedra around a direction approximately parallel to c1.The experiments were performed using hydrothermal solutions with KCl? 0.5 M; under these conditions, the quantity of incorporated chlorine does not exceed ?0300 ppm in the most receptive mica (annite) and is twenty times less in the less receptive ones (phlogopite, for example).These results are applied to natural biotites in porphyry copper deposits, metamorphic rocks and mafic rocks. We conclude that most natural biotites which have a chlorine content of 1000 ppm or more crystallized in equilibrium with a fluid phase with chloride contents of several molar (minimum 3 M).The consideration of micas applies in the same way to amphiboles. A clear correlation between the Cl content and XFe is observed which can be interpreted in terms of local structure of the minerals. The structural factors which favour the fixation of chlorine, a large anion are the same which favour the fixation of large alkali cations (replacement of Na by K). This explains the observed correlations between Cl and K in natural amphiboles.  相似文献   

8.
Samples located near the Oregon Dome anorthosite massif in the south-central Adirondack Mountains, New York contain the fluid-buffering mineral assemblages: amphibole + clinopyroxene + orthopyroxene + quartz or biotite + quartz + orthopyroxene + K-feldspar. These rocks were metamorphosed under granulite-facies conditions (T=725°–750°C, P=7.5 kbar) during the Grenville orogeny. The Mg-rich nature of amphiboles, micas, and pyroxenes allow accurate calculation of water activities because corrections for the effects of solid solution are relatively small. The activity of water was low during the peak of granulite-facies metamorphism, with H2O0.15±0.14. Wollastonite occurrences indicate that the CO2 was low (<0.3) in nearby rocks, demonstrating that large quantities of CO2 did not infiltrate in a pervasive manner. The combination of low H2O with low CO2 is consistent with the hypothesis that magmatic processes were dominant, generating dry, fluid-absent conditions.Abbreviations fi Fugacity of species i in a fluid - Xi mole fraction of component i in a phase - T temperature - P lithostatic pressure - P F fluid pressure - i x activity of component i phase X  相似文献   

9.
Skarns composed predominantly of Ca pyroxene, Ca amphibole, and biotite occur locally in the Grenville metamorphic terrain of the Canadian pre-Cambrian Shield. The enclosing rocks are Grenville gneisses and limestones, gabbroic rocks, veined gneisses, and granitic rocks. The metamorphic grade of the skarns is identical to that of the enclosing rocks, namely the upper region of the amphibolite facies.

Twelve skarn specimens were selected for chemical study. An investigation is made of the concentrations of Al, Fe, Mg, Mn, Ti, Ca, Na, K, Ba, V, Cr, Zr, Y, and Sc in eleven Ca pyroxenes, ten Ca amphiboles, and eleven biotites.

Consideration is given to the distribution of elements among coexisting minerals. Regular relationships appear when

1. (1) the concentration of an element in a mineral is related to the concentration of the element in a coexisting mineral by a linear or non-linear function

2. (2) the linear or non-linear function is itself a function of the concentration of another element in one or both of the coexisting minerals. These relationships indicate that, for the most part, minerals within each skarn specimen closely approached a state of chemical equilibrium.

A preliminary attempt is made to explain the distribution relationships in terms of crystal chemistry.  相似文献   


10.
The phase relations of pyroxenes, amphiboles and associated minerals in metamorphic rocks of the Franciscan Complex can be graphically depicted on a ternary diagram which has at its apices the metamorphic clinopyroxene end members, viz NaAl-NaFe3+-Ca(Fe2+, Mg). Phases are plotted by projection from a constant subassemblage of minerals. This analysis allows interpretation of the effects of pressure, temperature, bulk rock composition and fluid composition on stability of minerals within the Franciscan.Pyroxenes in meta-igneous rocks and metagraywackes have a limited compositional range and fall into two groups: the omphacites, with 50±5% diopside +hedenbergite component; and the jadeitic pyroxenes with 10±5% diopside+hedenbergite. Pyroxenes intermediate between these two groups are unstable relative to assemblages containing Na-amphibole+other minerals.Coexisting pyroxenes and amphiboles in eclogites and associated coarse blueschists comprise equilibrium assemblages, and the proportion of pyroxene to amphibole is a function of rock composition. Eclogites are stable at higher temperature than regionally developed fine-grained greenstones and blueschists in the Franciscan, and at higher pressure than amphibolites. X H2O fluid is not an important factor in the stability of Franciscan eclogite relative to amphibolite.  相似文献   

11.
Summary Clinopyroxene phenocrysts in six samples, representing the compositional range in the alkaline rocks of the region, range overall from aluminian titanian diopside (mg = Mg/[Mg + Fe t ] = 92) to aegirine (mg = 17), but Ca-pyroxenes are dominant (90% of 851 analyses), Ca-Na pyroxenes minor ( 10%) and Na-pyroxenes rare ( 1%). Pyroxenes in associated subalkaline rocks (dolerites and basalts) are lower-Ca augites of distinct trend. Al and Ti correlate positively in the alkaline rock pyroxenes, but negatively with Si, mirroring decreasing CaTiAl2O6 and CaSiAl2O6 components in more felsic host-rocks. Although the most evolved pyroxenes in each host-rock show increasingna (Na/[Na + Ca]) and Zr and decreasingmg as host-rock mg decreases, the most primitive pyroxenes in each host-rock do not change, implying they are not at equilibrium. Over 40 paired logitudinal and lateral traverses across 21 phenocrysts reveal very complex zoning, in which up to five growth zones can be recognized in one crystal, separated by either sharp contacts or gradual transitions. These individual zones may show one of seven zoning trends:normal (na asmg moving outwards towards the rim),reverse (na asmg ),inverse (na asmg ),converse (na asmg ),unzoned (no change),symmetric (na andmg display complementary and trends), oroscillatory (superimposed on normal, reverse or unzoned). Ten distinct crystal types can also be recognized, showing particular sequences of zoning trends: for example, Type 1 shows a green, relatively sodic core surrounded by a more primitive rim or overgrowth, and has similar longitudinal and lateral zoning; whereas Type 6 shows extremely erratic variations which differ longitudinally and laterally. Up to four of these types were found in one host-rock, with little pattern in their distribution between different host-rocks. These pyroxenes are believed to record an intricate history of stop-start differentiation, complicated by magma-mixing, entry or disappearance of coprecipitating phases, and inheritance of high-pressure precipitates. Apparently random superimposed variations of Al, Ti and Si within some individual growth zones most probably reflect kinetic (disequilibrium) effects, due to rapid growth and/or supercooling.
Alkaligesteine und Karbonatite von Amba Dongar und Umgebung Deccan Alkali-Provinz, Gujarat, Indien. 2. Komplex zonierte Klinopyroxenkristalle
Zusammenfassung Klinopyroxenkristalle in sechs Proben, die das ganze Spektrum der Zusammensetzung der Alkaligesteine des Gebietes repräsentieren, schwanken von Aluminium-Titandiopsid (mg = Mg/[Mg + Fe t ] = 92) bis Aegirin (mg = 17), aber C-Pyroxene dominieren (90% von 851 Analysen). Ca-Na-Pyroxene sind Nebengemengteile (10%) und Na-Pyroxene sind selten ( 1%). Pyroxene in assoziierten subalkalischen Gesteinen (Dolerite und Basalte) sind Ca-arme Augite eines eigenständigen Trendes. Al und Ti korrelieren positiv in den Pyroxenen der Alkaligesteine, aber negativ mit Si, und dies spiegelt abnehmende CaTiAl2O6 und CaSiAl2O6 Komponenten in den mehr felsischen Wirtsgesteinen wider. Obwohl Pyroxene in jedem Wirtsgestein zunehmende na-Werte (Na/[Na + Ca]) und Zr-Gehalte und mit demmg des Wirtsgesteines auch abnehmendemg-Werte zeigen, lassen die primitivsten Pyroxene in jedem Wirtsgestein keine Änderung erkennen. Dies weist darauf hin, daß sie nicht im Gleichgewicht sind. Über vierzig paarweise angelegte Längs- und Quertraversen über 21 Kristalle zeigen sehr komplexen Zonarbau, in dem bis zu fünf Wachstumszonen in einem Kristall erkannt werden können, die entweder von scharfen Kontakten oder von graduellen Übergangszonen getrennt werden. Diese individuellen Zonen können einen der folgenden sieben Trends erkennen lassen: Normal (na ;mg ; von innen gegen den Rand zu), reverse (na ,mg ), invers (na undmg ), konvers (na ,mg ), unzoniert (keine Änderung), symmetrisch (na undmg zeigen komplementäre und Trends), oder oszillierend (überlagert den normalen, reversen oder unzonierten Trend). Weiters können zehn definierte Kristalltypen erkannt werden, die besondere Abfolgen von Trends der Zonierung erkennen lassen. Zum Beispiel zeigt Typ 1 einen grünen, relativ Na-reichen Kern, umgeben von einem mehr primitiven Rand oder Überwachsungen, wobei die Zonierung in Längs- und Querrichtung ähnlich ist. Demgegenüber zeigt Typ 6 außerordentlich unregelmäßige Zonierungen, die in Längs- und Querschnitten verschieden sind. Bis zu vier dieser Typen wurden in einem Wirtsgestein nachgewiesen, und sie ließen keine deutlichen Verteilungsmuster zwischen verschiedenen Wirtsgesteinen erkennen. Es wird angenommen, daß diese Pyroxene eine komplexe geschichte von stop-start Differentiation wiedergeben, die durch Magmamischung, durch die Zufuhr oder das Verschwinden von gleichzeitig ausfallenden Phasen und durch die Übernahme von Hochdruck-Bildungen weiter kompliziert wird. Unregelmäßig überlagerte Variationen von Al, Ti und Si innerhalb einzelner Wachstumszonen reflektieren sehr wahrscheinlich kinetische (Ungleichgewicht) Effekte, die auf sehr rasches Wachstum und/oder Überkühlung zurückgehen.

Deceased

With 11 Figures  相似文献   

12.
大别山典型燕山期侵入体中矿物成分特征及其地质意义   总被引：4，自引：0，他引：4  
分析了大别造山带核部典型燕山期侵入体中的斜长石、黑云母和角闪石的化学成分和成因特点,并从矿物平衡角度讨论了典型侵入体岩石成因。结果表明：（１）石鼓尖侵入岩中,斜长石成分较稳定,共生角闪石和黑云母为岩浆平衡结晶的矿物;（２）天堂寨和九资河侵入岩中,部分斜长石和黑云母可能为深蚀残留矿物,角闪石属于火成岩区的新生矿物,可能为斜长石和黑云母发生融反应所形成;（３）三个侵入体的岩石均为岩浆成因。  相似文献   

13.
Zdeněk Vejnar 《Lithos》1975,8(1):59-68
The chemical composition of Ca-pyroxenes and calcium-rich amphiboles shows that the gabbroic rocks of the Central Bohemian Pluton contain primary igneous mineral associations as well as associations produced by later recrystalization. The partitioning of Mg and Fe between co-existing pyroxenes and hornblendes suggests that the temperature of crystal-liquid equilibrium corresponding to the formation of the gabbro was about 300–400°C higher than the temperature of the later recrystallization.  相似文献   

14.
The migmatitic rocks exposed in Hafafit and Feiran areas exhibit some migmatitic structures as the banded, agmatic, boudinage and schlieren structures. The dominant type of these structures is the stromatic migmatites. Electron microprobe analyses of plagioclases, biotites and amphiboles from Hafafit and Feiran areas, in the Eastern Desert and Sinai, Egypt, are carried out and the metamorphic conditions are discussed. The present study revealed marked differences in the composition of plagioclases, biotites and amphiboles from Hafafit and Feiran localities. The obtained data indicated that plagioclases of the Feiran migmatites are of andesine and oligoclase composition, and display anorthite content from An20 to An38; whereas the Hafafit migmatites show a wider range of plagioclases from An10 to An60, and therefore plagioclases have labradorite, andesine and oligoclase composition. This may be due to the slow rate of the crystallisation processes. The analyses indicated that biotites of the studied areas are of metamorphic origin showing significant variation in Fe–Mg. It is worth mentioning that biotites from Hafafit migmatites have Mg–biotite composition while that of Feiram migmatites have Fe–biotite composition. High Mg and low Fe contents in biotite suggest higher crystallisation temperature. The composition of amphiboles in Hafafit migmatites is ferro-tschermakitic hornblende, while amphiboles from Feiram migmatites are magnesio-hornblende. High Ti content in the hornblende of Feiran migmatites suggests that they were formed at slightly higher temperatures and lower pressure than the Hafafit migmatites (i.e. Feiram migmatites and Hafafit migmatites were formed at granulite and amphibolite facies, respectively). Discrimination diagrams show that the muscovite is of secondary origin. Moreover, the present study confirmed that these migmatites are mainly formed by metamorphic differentiation via partial melting.  相似文献   

15.
Palaeoproterozoic (ca 2,480 Ma) felsic magmatism of Malanjkhand region of central Indian Precambrian shield, referred to as Malanjkhand granitoids (MG), contain xenoliths of country rocks and mesocratic to melanocratic, fine-grained porphyritic microgranular enclaves (ME). The shape of ME is spheroidal, ellipsoidal, discoidal, elongated, and lenticular, varying in size from a few centimeters to about 2 m across. The contact of ME with the host MG is commonly sharp, crenulate, and occasionally diffuse, which we attribute to the undercooling and disaggregation of ME globules within the cooler host MG. The ME as well as MG show hypidiomorphic texture with common mineral Hbl-Bt-Kfs-Pl-Qtz assemblage, but differ in modal proportions. The variation in minerals' composition, presence of apatite needles, elongated biotites, resorbed plagiclase, ocellar quartz, and other mafic–felsic xenocrysts strongly oppose the restite and cognate origins of ME. Compositions of plagioclases (An3–An29), amphiboles (Mg/Mg+Fe2+=0.55–0.69), and biotites (Mg/Mg+Fe2+=0.46–0.60) of ME are slightly distinct or similar to those of MG, which suggest partial to complete equilibration during mafic–felsic magma interactions. Al-in-amphibole estimates the MG pluton emplacement at ca 3.4 ± 0.5 kbar, and therefore, magma mixing and mingling must have occurred at or below this level. The substitution in biotites of ME and MG largely suggests subduction-related, calc–alkaline metaluminous (I-type) nature of felsic melts. Most major and trace elements against SiO2 produce near linear variation trends for ME and MG, probably generated by the mixing of mafic and felsic magmas in various proportions. Trace including rare earth elements patterns of ME–MG pairs, however, show partial to complete equilibration, most likely governed by different degrees of elemental diffusion. The available evidence supports the model of ME origin that coeval mafic (enclave) and felsic (MG) magmas produced a hybrid (ME) magma layer, which injected into cooler, partly crystalline MG, and dispersed, mingled, and undercooled as ME globules in a convectively dynamic magma chamber.  相似文献   

16.
Kinetic studies of isothermal heating experiments (600–800° C) on aluminous pyroxenes (Mg0.942Fe 0.880 2+ Fe 0.068 3+ Mn0.016Ca0.010Al0.084) (Si1.848Al0.152) permit the determination of rate constant of isothermal disordering as 2.5457 E13(±1.4 E13) min?1. The activation energy is determined as 278 (±23) kJ/mol. Data on two other aluminous pyroxenes at 700° C indicate that the rate constant decreases significantly with increasing amount of trivalent cations. There is a similar but reverse correlation between the concentration of trivalent cations and the Fe2+-Mg equilibrium distribution between sites. The site distribution coefficient increases with increasing concentration of trivalent cations at constant temperature.  相似文献   

17.
Gabbroic intrusions of the El-Aradiya area are a part of the Neoproterozoic basement cropping out in the central Eastern Desert of Egypt. They are composed mainly of gabbroic cumulates (diopside-plagioclase cumulate and plagioclase-augite cumulate) and fine-grained noncumulate gabbro. Mineral chemistry data indicate that the plagioclase core compositions of the gabbroic cumulates range between An90 and An60, whereas fine-grained noncumulate gabbro plagioclase core compositions are An61−56 and rim compositions are An54−42. The clinopyroxenes are diopside and augite in the gabbroic cumulate, and augite in the fine-grained noncumulate gabbro. Chemical re-equilibration between pyroxenes of gabbroic cumulates vary from 1150-900°C and for fine-grained noncumulate gabbro range from 1200-1100°C. The amphiboles are calcic, varying from tschermakite and tschermakitic hornblende, and Mg-hornblende in the gabbroic cumulate and only Mg-hornblende in the fine-grained noncumulate gabbro. They indicate an island-arc tholeiitic setting for gabbroic intrusions of the El-Aradiya area. Major and trace element data suggest arc tholeiite characters, a comagmatic suite and subduction-related magma with enrichment of LILE and depletion in HFSE relative to MORB. The estimated parent magma is similar to tholeiitic Aleutian arc primary magma. The gabbroic intrusions are analogous to intrusions emplaced in an immature island-arc setting in which the oceanic crust was thin.  相似文献   

18.
In the Sesia Zone of the Western Alps, Italy, early Alpine blueschist to eclogite facies metamorphism of rocks of quartzofeldspathic composition has produced the same high-pressure assemblage of; quartz, Na-pyroxene, Na-amphibole, paragonite, phengite, zoisite, garnet, magnetite, sphene and Fe-sulphide (=the QFS assemblage) over an area (> 150 km2. Relative gradients in pressure and temperature over this region are reflected in the variations in mineral chemistries of the individual phases of the quartzofeldspathic assemblage through continuous reactions. Mineralogical discontinuities do not occur in the QFS assemblage of this region. Increases in the Jadeite content of the pyroxenes (X Jd 0.48 to X Jd 0.93) and in the glaucophane content of the amphiboles (X Gl 0.89 to X Gl 0.96) occur from the southwest to the northeast of the region studied. Analysis of coexisting garnets and pyroxenes indicate that the compositional variation of amphiboles and pyroxenes is associated with a decrease in the grossular component of the coexisting garnet. Zoned pyroxenes and garnets, together with the regional trends in mineral chemistries suggest that the evolution of the QFS assemblage with increasing pressure may be modelled by pressure-sensitive continuous reactions in which amphibole, zoisite and the more jadeitic pyroxene constitute the high-pressure assemblage. Chemographic constraints permit the positioning in pressure/temperature space of the compositional isopleths of those model continuous reactions involving these phases which meet the textural and chemical criteria observed in the natural assemblages. The low dP/dT slope (–20 bars/° C) of these isopleths causes the continuous reactions to be useful for geobarometric calculations at pressures above the absolute breakdown of albite to jadeite plus quartz. In addition the pseudobinary loops for the other continuous reactions which are potentially useful geobarometers and involve either the NaAlCa–1Mg–1 exchange or the MgCa–1 exchange are calculated. Comparison of mineral chemistries with the isopleths yields a relative barometric scheme for the localities studied. With these barometric observations, it is possible to show that the P-T path which the Sesia body travelled towards the final recorded state was one of increasing pressure. Other blueschist and eclogite occurrences from Syros and Sifnos which contain rocks of quartzofeldspathic composition are also examined.  相似文献   

19.
Abstract Sodic amphiboles are common in Franciscan type II and type III metabasites from Cazadero, California. They occur as (1) vein-fillings, (2) overgrowths on relict augites, (3) discrete tiny crystals in the groundmass, and (4) composite crystals with metamorphic Ca–Na pyroxenes in low-grade rocks. They become coarse-grained and show strong preferred orientation in schistose high-grade rocks. In the lowest grade, only riebeckite to crossite appears; with increasing grade, sodic amphibole becomes, first, enriched in glaucophane component, later coexists with actinolite, and finally, at even higher grade, becomes winchite. Actinolite first appears in foliated blueschists of the upper pumpellyite zone. It occurs (1) interlayered on a millimetre scale with glaucophane prisms and (2) as segments of composite amphibole crystals. Actinolite is considered to be in equilibrium with other high-pressure phases on the basis of its restricted occurrence in higher grade rocks, textural and compositional characteristics, and Fe/Mg distribution coefficient between actinolite and chlorite. Detailed analyses delineate a compositional gap for coexisting sodic and calcic amphiboles. At the highest grade, winchite appears at the expense of the actinolite–glaucophane pair. Compositional characteristics of Franciscan amphiboles from Ward Creek are compared with those of other high P/T facies series. The amphibole trend in terms of major components is very sensitive to the metamorphic field gradient. Na-amphibole appears at lower grade than actinolite along the higher P/T facies series (e.g. Franciscan and New Caledonia), whereas reverse relations occur in the lower P/T facies series (e.g. Sanbagawa and New Zealand). Available data also indicate that at low-temperature conditions, such as those of the blueschist and pumpellyite–actinolite facies, large compositional gaps exist between Ca- and Na-amphiboles, and between actinolite and hornblende, whereas at higher temperatures such as in the epidote–amphibolite, greenschist and eclogite facies, the gaps become very restricted. Common occurrence of both sodic and calcic amphiboles and Ca–Na pyroxene together with albite + quartz in the Ward Creek metabasites and their compositional trends are characteristic of the jadeite–glaucophane type facies series. In New Caledonia blueschists, Ca–Na pyroxenes are also common; Na-amphiboles do not appear alone at low grade in metabasites, instead, Na-amphiboles coexist with Ca-amphiboles throughout the progressive sequence. However, for metabasites of the intermediate pressure facies series, such as those of the Sanbagawa belt, Japan and South Island, New Zealand, Ca–Na pyroxene and glaucophane are not common; sodic amphiboles are restricted to crossite and riebeckite in composition and clinopyroxenes to acmite and sodic augite, and occur only in Fe2O3-rich metabasites. The glaucophane component of Na-amphibole systematically decreases from Ward Creek, New Caledonia, through Sanbagawa to New Zealand. This relation is consistent with estimated pressure decrease employing the geobarometer of Maruyama et al. (1986). Similarly, the decrease in tschermakite content and increase in NaM4 of Ca-amphiboles from New Zealand, through Sanbagawa to New Caledonia is consistent with the geobarometry of Brown (1977b). Therefore, the difference in compositional trends of amphiboles can be used as a guide for P–T detail within the metamorphic facies series.  相似文献   

20.
Amphibolite facies metamorphic grade gives way southward to the granulite grade in southern Karnataka, as acid gneisses develop charnockite patches and streaks and basic enclaves develop pyroxenes. Petrologic investigations in the transitional zone south of Mysore have established the following points:
  1. The transition is prograde. Amphibole-bearing gneisses intimately associated with charnockite at Kabbal and several similar localities are not retrogressive after charnockite, as proved by patchy obliteration of their foliation by transgressive, very coarse-grained charnockite, high fluorine content of biotite and amphibole in gneisses, and high large-ion lithophile element contents in gneisses and charnockites. These features are in contrast to very low fluorine in retrogressive amphiboles and biotites, very low large-ion lithophile element contents, and zonal bleaching of charnockite, in clearly retrogressive areas, as at Bhavani Sagar, Tamil Nadu.
  2. Metamorphic temperatures in the transitional areas were 700°–800° C, pressures were 5–7 kbar, and H2O pressures were 0.1–0.3 times total pressures, based on thermodynamic calculations using mineral analyses. Dense CO2-rich fluid inclusions in the Kabbal rocks confirm the low H2O pressures at the first appearance of orthopyroxene. Farther to the south, in the Nilgiri Hills and adjacent granulite massif areas, peak metamorphic temperatures were 800°–900° C, pressures were 7–9 kbar, and water pressures were very low, so that primary biotites and amphiboles (those with high F contents) are rare.
  3. The incipient granulite-grade metamorphism of the transitional areas was introduced by a wave of anatexis and K-metasomatism. This process was arrested by drying out under heavy CO2 influx. Charnockites so formed are hybrids of anatectic granite and metabasite, of metabasite and immediately adjacent gneiss, or are virtually isochemical with pre-existing gneiss despite gross recrystallization to granulite mineralogy. These features show that partial melting and metasomatism are attendant, rather than causative, in charnockite development. Copious CO2 from a deep-crustal or mantle source pushed ahead of it a wave of more aqueous solutions which promoted anatexis. Granulite metamorphism of both neosome and paleosome followed. The process is very similar to that deduced for the Madras granulites by Weaver (1980). The massif charnockites, for the most part extremely depleted in lithophile minor elements, show many evidences of having gone through the same process.
A major problem remaining to be solved is the origin of the large amount of CO2 needed to charnockitize significant portions of the crust. The most important possibilities include CO2 from carbonate minerals in a mantle “hot spot” or diapir, from emanations from a crystallizing basaltic underplate, or from shelf sediments trapped at the continent-continent interface in continental overthrusting. Ancient granulite massifs may be such suture zones of continental convergence.  相似文献   

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