Parageneses and compositions of amphiboles from Franciscan jadeite–glaucophane type facies series metabasites at Cazadero, California

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.     

Sodic pyroxenes from metabasites in the eastern mediterranean

The compositions of sodic pyroxenes from blueschist metabasites in Northwest Turkey were investigated by electronprobe microanalysis. These are compared with sodic pyroxenes from high-grade blueschist terrains and eclogites with special reference to the island of Syros in Greece. Pyroxenes from lawsonite zone metabasites in Northwest Turkey are chloromelanites, aegerine augites and aegerine jadeites with the acmite contents ranging from 65% down to 30%. Epidote-garnet bearing high-grade blueschist metabasites of Syros on the other hand contain omphacite with the acmite content less than 30%. All the analyzed sodic pyroxenes from eclogites and high-grade blueschists in the literature are also omphacites with low acmite contents. It is argued that the acmite content of the sodic pyroxene decreases with rising temperature of metamorphism. This is almost entirely related to the appearance of epidote as an additional ferric ion bearing phase with an increase in temperature.     

Chemical types of amphiboles from the Tyrnyauz deposit

Based on the results of microprobe analyses, six groups of calcium amphiboles were distinguished for the Tyrnyauz deposit. Group I (mainly edenite) includes amphiboles of hornfels and periskarn rocks. Groups II-VI (actinolite-hastingsite series) are related to post-skarn metasomatic rocks of the productive stage after hornfels (II), the tonalite and plagiogranite complex (III), ultrabasic rocks (IV), pyroxene-plagioclase periskarn rocks (V), and skarn (VI). Group IV is represented by actinolite; group VI, by hastingsite; groups II, III, and V, by hornblende varieties.     

Sodic amphiboles and pyroxenes from fenites in East Africa

During alkali metasomatism of the country-rock associated with ijolite-carbonatite complexes the development of sodic amphibole and/or pyroxene is characteristic. In this paper, some new chemical analyses of these minerals, together with published analyses from fenites of Kenya, Uganda and Tanzania, include those of co-existing pairs of amphibole and pyroxene. The common amphiboles of the fenites are magnesioarfvedsonites with 100 Mg: Mg+Fe+Mn ranging from 67 to 36. They co-exist with aegirines having 0.75 to 0.89 ions Fe⁺³. Most of these minerals are poor in Ca; co-existing pairs tend to show corresponding increases in Ca and in Fe⁺². In the syenitic fenites of Tororo and Budeda, considered to have formed at higher temperatures, the stable mineral is aegirine-augite. New analyses of richterite, magnesioarfvedsonite and aegirine from carbonate-rich rocks are also presented, and the relation between fenites and carbonatites is discussed.     

Greenschist amphiboles from Haast river,New Zealand

A section across the Haast Schist Group in the Southern Alps of New Zealand shows a sequence of metamorphosed eugeosynclinal sediments. Meta-basic rocks (greenschists) have been studied to determine the nature of the actinolite-hornblende transition and to investigate the change in amphibole composition through the Metamorphic Facies Series.Electron microprobe analyses of 21 representative amphiboles, including 3 amphibole pairs can be shown to support theories of a miscibility break in the calciferous amphibole solid solution series. The existence of a miscibility break is further supported by the widespread appearance, even at low metamorphic grades, of exsolution lamellae in actinolite and hornblende amphiboles.Amphibolite facies amphiboles differ from greenschist facies amphiboles in that (a) there are increased amounts of Ti entering the lattice and (b) that there is an increased occupancy of the A site at higher metamorphic grades.     

A new petrogenetic grid for low-grade metabasites

Abstract We have used internally-consistent thermodynamic data to present calculated phase equilibria for the system Na₂O-CaO-MgO-Al₂O₃-SiO₂-H₂O (NCMASH), in the range 0–500° C and 0.1–10 kbar, involving the phases anorthite, glaucophane, grossular, heulandite, jadeite, laumontite, lawsonite, paragonite, prehnite, pumpellyite, stilbite, tremolite, wairakite, zoisite with excess albite, clinochlore, quartz and pure water. Average activity terms derived from published mineral chemical data were included for clinochlore, glaucophane, prehnite, pumpellyite, tremolite, and zoisite. The new petrogenetic grid delineates stability fields and parageneses of common index minerals in zeolite, prehniteactinolite, prehnite-pumpellyite, pumpellyite-actinolite, blueschist and greenschist facies metabasites. The stability fields of mineral assemblages containing prehnite, pumpellyite, epidote, actinolite (+ albite + chlorite + quartz) were analysed in some detail, using activity data calculated from five specific samples. For example, the prehnite-actinolite facies covers a P-T field ranging from about 220 to 320° C at pressures below 4.5 kbar. The transition from the prehnite-actinolite and pumpellyite-actinolite to greenschist facies occurs at about 250–300° C at 1–3 kbar and at about 250–350° C at 3–8 kbar. P-T fields of individual facies overlap considerably due to variations in chemical composition.     

Coexisting amphiboles in an eclogite from the Western Alps: new constraints on the miscibility gap between sodic and calcic amphiboles

Abstract Crystal-chemical relationships between coexisting sodic and calcic amphiboles have been studied in eclogitic metagabbros from the Aosta Valley, Western Alps. Textural analysis gives evidence of three successive high-pressure parageneses:
1. Pre-kinematic high-grade blueschist assemblages, preserved as polymineralic inclusions in garnet cores and made of glaucophane and actinolite (stage A).
2. Synkinematic eclogite assemblages, composed of garnet + omphacite + glaucophane ± actinolite ± white mica ° Clinozoisite + quartz + rutile (stage B).
3. Post-kinematic epitactic overgrowths of barroisitic amphibole on glaucophane and actinolite (stage C).
P–T conditions of the eclogitic metamorphism have been estimated at around 500–550°C, 16 kbar.
Glaucophane and actinolite coexist as discrete grains in stage A and B assemblages. This texture and the chemistry of the amphiboles unambiguously denotes the existence of a miscibility gap between sodic and calcic amphiboles (from Na^M4= 0.80 in actinolite to Na^M4= 1.70 in glaucophane at T = 500–550°C). A comparison with published analyses allows a new solvus along the glaucophane–actinolite join to be drawn.
The later barroisitic amphibole (stage C) exhibits strong chemical zonation indicating disequilibrium growth. This amphibole cannot either be used to define a miscibility gap with glaucophane or actinolite or be considered as an intermediate stage between these two end-members.     

Sub-greenschist facies assemblages of metabasites from south-eastern Peloritani range (NE-Sicily)

Summary Pre-Hercynian magmatic rocks are widespread in the Palaeozoic basement of the Peloritani range. The metabasites of the Mongiuffi-Melia and Gallodoro areas represent the largest and the most important lower-Ordovician magmatic products of this range. These rocks were metamorphosed during the Hercynian event and preserve relict igneous minerals and textures. A detailed study of the metamorphic assemblages has allowed the identification of two stages of metamorphic crystallisation; they are mainly distinguished by the differentXCO₂ of the fluid phase. The first metamorphic event produced three calcite-free sub-greenschist facies assemblages that contain ubiquitous quartz+albite+titanite+chlorite+epidote along with pumpellyite or prehnite or actinolite. The second metamorphic episode produced a Calcite+Chlorite assemblage, non-diagnostic to evaluate P-T conditions of metamorphism. The first stage assemblages are only preserved in small domains of the rock. As even very low amounts of CO₂ in the fluid phase drastically inhibit the formation of diagnostic sub-greenschist facies calc-silicate assemblages, it appears that a more CO₂-rich fluid must have been introduced during the second event. We suggest that this introduction of more CO₂-rich fluid occurred during the development of S₂ crenulation cleavage.

---

Sub-grünschieferfazielle Mineralvergesellschaftungen in Metabasiten der südöstlichen Peloritani Range (NE Sizilien)

Zusammenfassung Prähercynische magmatische Gesteine sind weitverbreitet im paläozoischen Basement der Peloritani Range. Die Metabasite aus dem Mongiuffi-Melia und dem Gallodoro Gebiet sind die größten und wichtigsten magmatischen Produkte des unteren Ordoviziums in diesem Gebiet. Sie wurden während der hercynischen Orogenese metamorphisiert und sie bewahren reliktische magmatische Minerale und Strukturen. Eine Detailstudie der metamorphen Mineralvergesellschaftungen erlaubt die Identifikation von zwei metamorphen Kristallisationsstadien, die sich hauptsächlich im XCO₂ der fluiden Phase unterscheiden. Das erste Ereignis resultierte in der Bildung von drei Calcit-freien sub-grünschieferfaziellen Mineralvergesellschaftungen, die verbreitet Quarz+Albit+Titanit+Chlorit+Epidot mit Pumpellyit oder Prehnit oder Aktinolith führen. Die zweite metamorphe Episode führte zur Bildung der Vergesellschaftung Calcit+Chlorit; diese ist für die Abschätzung der P-T Bedingungen der Metamorphose ungeeignet. Die erste Vergesellschaftung ist nur in kleinen Domänen in den Gesteinen erhalten geblieben. Da bereits sehr geringe Mengen an CO₂ in der fluiden Phase die Bildung der diagnostischen sub-grünschieferfaziellen kalk-silikatischen Mineralassoziation verhindern, scheint es, daß das CO₂-reiche Fluid während des zweiten Stadiums zugeführt wurde. Wir meinen, daß die Zufuhr dieser CO₂-reichen Fluide während der Entwicklung der S2 Krenulationsschieferung erfolgt sein muß.

---

---

With 6 Figures     

Petrology of lawsonite-, pumpellyite- and sodic amphibole-bearing metabasites from north-east Oman

The assemblages chlorite-pumpellyite-lawsonite-albite-quartz, chlorite-lawsonite-quartz-epidote and chlorite-epidote-albite-quartz occur in metabasaltic blocks and veins in a metamorphosed tectonic mélange in the structurally highest unit of the autochthonous and parautochthonous section underlying the Semail ophiolite in Saih Hatat, north-east Oman. The pre-Permian basement of this section contains mafic units characterized by the assemblage crossite-epidote-chlorite-quartz-albite /el actinolite. These assemblages indicate a down-section increase in metamorphic grade from 'lawsonite-albite facies' conditions in the mélange to 'epidote-blueschist' facies conditions in the basement.
Application of empirically and experimentally based thermobarometers as well as petrogenetic grids calculated for a model basaltic system indicates that the P-T conditions of metamorphism ranged from 3 to 6 kbar and 250 to 300 C for the mélange and P > 6.8 kbar, T > 310 C for the basement units. Textural relations interpreted in the context of petrogenetic grids indicate that these units followed clockwise P-T paths of evolution. The estimated P-T conditions and down-section increase in metamorphic grade in central, western and northern Saih Hatat are consistent with the hypothesis relating metamorphism to the Late Cretaceous tectonic loading of the continental margin by an ophiolite slab < 18 km in thickness. These results contrast with field and petrological observations documented for blueschists and eclogites exposed along the eastern coast of Saih Hatat which may have formed at an earlier stage in response to an Early Cretaceous collisional event.     

Shock-metamorphic features in amphiboles from the Xiuyan crater of China

Amphibole-bearing gneiss fragments are common in the impact breccias of the Xiuyan crater, China. Three kinds of amphibole-bearing gneiss fragments with different shock-metamorphic levels have been identified. Shock-metamorphic features of amphiboles in these gneisses were investigated in situ by optical microscope, electron microprobe, Raman spectroscopy, and X-ray diffraction. Amphiboles in the weakly shocked gneiss (shock pressure less than 10 GPa) basically remain intact. Amphiboles in the moderately shocked gneiss (shock pressure range between 35 and 45 GPa) show strong deformation, reduced optical interference color, and partial loss of OH^?. In the strongly shocked gneiss (shock pressure above 50 GPa), amphiboles are completely melted and dendritic pyroxenes crystallize from the melt. The formation of dendritic pyroxenes shows nearly complete loss of water in the amphibole melt at shock-induced high temperature above 1,500 °C. The occurrence of both diopside and pigeonite dendrites crystallized in the same amphibole melt shows inhomogenous melt composition and rapid cooling of the melt.     

Chemical etching of amphiboles and pyroxenes

Chemical etching of defect structures in pyroxenes and amphiboles has been investigated. Many features, such as very thin (～1 micrometer) exsolution lamellae not observed by transmission optical microscopy of thin sections, have been observed in reflected light after chemical etching of cleaved or polished crystal surfaces. A new feature in the microstructure of pyroxenes, not previously reported in the literature, has been revealed by one of the etchants.     

Statistical chemistry of calcic amphiboles

Principal components analysis is used to study the chemistry of 639 calcic amphiboles. Eigenvectors representing multiple partial correlation coefficients give various sets of substitutional relationships. The relative significance of each set can be noted by the percent variation of the data it represents. The highest percent variation (36%) is associated with the substitutions $$Si + Mg \rightleftharpoons Al^{IV} + Al^{VI} + Ti + Fe^{3 + } + Fe^{2 + } + Na + K$$ . Other expected substitutions among the ions such as Al^IV + Na ? Si, the positive correlation between Al^IV and Al^VI etc. are shown statistically. The substitution of Al in T ₁ and T ₂ positions imposes an ordering in the M ₁, M ₂ and M ₃ sites. Variability of OH in the amphiboles is found to be significant. There is no definite correlation between OH and Fe³⁺ but OH and Ti are positively correlated. Under certain conditions and provided the concentration of Al^IV does not change significantly, Fe and Mg may be assumed to mix ideally in the amphibole solid solution.     

Equilibrium coexistence of three amphiboles

Electron probe and wet chemical analyses of amphibole pairs from the sillimanite zone of central Massachusetts and adjacent New Hampshire indicated that for a particular metamorphic grade there should be a restricted composition range in which three amphiboles can coexist stably. An unequivocal example of such an equilibrium three amphibole rock has been found in the sillimanite-orthoclase zone. It contains a colorless primitive clinoamphibole, space group P2₁/m, optically and chemically like cummingtonite with blue-green hornblende exsolution lamellae on (100) and (¯101) of the host; blue-green hornblende, space group C2/m, with primitive cummingtonite exsolution lamellae on (100) and (¯101) of the host; and pale pinkish tan anthophyllite, space group Pnma, that is free of visible exsolution lamellae but is a submicroscopic intergrowth of two orthorhombic amphiboles. Mutual contacts and coarse, oriented intergrowths of two and three host amphiboles indicate the three grew as an equilibrium assemblage prior to exsolution. Electron probe analyses at mutual three-amphibole contacts showed little variation in the composition of each amphibole. Analyses believed to represent most closely the primary amphibole compositions gave atomic proportions on the basis of 23 oxygens per formula unit as follows: for primitive cummingtonite (Na_0.02Ca_0.21 ^– Mn_0.06Fe²⁺ _2.28Mg_4.12Al_0.28) (Al_0.17Si_7.83), for hornblende (Na_0.35Ca_1.56Mn_0.02Fe_1.71Mg_2.85Al_0.92) (Al_1.37Si_6.63), and for anthophyllite (Na_0.10Ca_0.06Mn_0.06Fe_2.25Mg_4.11Al_0.47) (Al_0.47Si_7.53). The reflections violating C-symmetry, on X-ray single crystal photographs of the primitive cummingtonite, are weak and diffuse, and suggest a partial inversion from a C-centered to a primitive clinoamphibole. Single crystal photographs of the anthophyllite show split reflections indicating it is an intergrowth of about 80% anthophyllite and about 20% gedrite which differ in their b crystallographic dimensions. Split reflections are characteristic of all analyzed orthorhombic amphiboles so far examined from Massachusetts and New Hampshire except the most aluminous gedrites, and the relative intensity of the gedrite reflections is roughly proportional to the degree of Na and Al substitution. Thin sections of a few of these anthophyllite specimens show lamellae parallel to (010) that are just resolved with a high power objective.Publication approved by the Director, U.S. Geological Survey.     

Thermodynamic study of calcic amphiboles

The paper reports original thermochemical data on six natural amphibole samples of different composition. The data were obtained by high-temperature melt solution calorimetry in a Tian–Calvet microcalorometer and include the enthalpies of formation from elements for actinolite Ca_1.95(Mg_4.4Fe _0.5 ²⁺ Al₀₁)[Si_8.0O₂₂](OH)₂(–12024 ± 13 kJ/mol) and Ca_2.0(Mg_2.9Fe _1.9 ²⁺ Fe _0.2 ³⁺ )[Si_7.8Al_0.2O₂₂](OH)₂, (–11462 ± 18 kJ/mol), and Na_0.1Ca_2.0(Mg_3.2Fe _1.6 ²⁺ Fe _0.2 ³⁺ )[Si_7.7Al_0.3O₂₂](OH)₂ (–11588 ± 14 kJ/mol); for pargasite Na_0.5K_0.5Ca_2.0-(Mg_3.4Fe _1.8 ²⁺ Al_0.8)[Si_6.2Al_1.8O₂₂](OH)₂ (–12316 ± 10 kJ/mol) and Na_0.8K_0.2Ca_2.0(Mg_2.8Fe _1.3 ³⁺ Al_0.9) [Si_6.1Al_1.9O₂₂](OH)₂ (–12 223 ± 9 kJ/mol); and for hastingsite Na_0.3K_0.2Ca_2.0(Mg_0.4Fe _1.3 ²⁺ Fe _0.9 ³⁺ Al_0.2) [Si_6.4Al_1.6O₂₂](OH)₂ (?10909 ± 11 kJ/mol). The standard entropy, enthalpy, and Gibbs free energy of formation are estimated for amphiboles of theoretical composition: end members and intermediate members of the isomorphic series tremolite–ferroactinolite, edenite–ferroedenite, pargasite–ferropargasite, and hastingsite.     

Clustering of cations in amphiboles

The OH^? stretching frequencies of clino-amphiboles are known to depend on the cations to which the OH^? is co-ordinated, and the intensities of the corresponding infra-red (ir) absorption bands have been used to obtain evidence as to the occupancy of the M1 and M3 sites. However, the possible effects on the method arising from clustering together of like cations, or of the mutual avoidance of like cations (anti-clustering), have not hitherto been explicitly analysed. A model is set up which permits these to be systematically explored. The results are exemplified for occupation of M1 and M3 by (Fe, Mg). Clustering of Fe increases the frequency of both Fe₃ and Mg₃ triads, though not equally, and the effect of anti-clustering is in the opposite sense. The effect on the frequencies of MgFe₂ and Mg₂Fe triads is much more complicated and the sense of the changes depends on both the overall Fe content and on the degree of clustering or anti-clustering.     

Characteristics of asbestiform and non-asbestiform calcic amphiboles

In terms of morphology there are four major types of calcic amphibole; massive, prismatic, finely acicular and asbestos. Representatives of each of these types have been examined by optical microscopy, X-ray diffraction, scanning and transmission electron microscopy, and electron probe microanalysis. Massive specimens (nephrite) consist of randomly oriented clusters of fine, roughly lath-shaped, sub-microscopic crystals; within each cluster the lath lengths (z) are approximately aligned but neighbouring laths are rotated with respect to one another. Finely acicular specimens (“byssolites”) have well-formed crystals bounded mainly by {110} (100) and (010) faces and characteristically have striations parallel to their lengths. Asbestiform varieties range from finer (flexible) to coarser (more brittle) specimens and many specimens contain a mixture of fine and coarse fibrils. The fibrils in a bundle are aligned parallel to z but are in a range of azimuthal orientations. It is inferred that they are formed by multiple independent nucleation and growth parallel to z rather than through parting or cleavage on {110} planes. (100) defect or twin planes, or on (010) planar defects.

The {110} cleavage in amphiboles is well reported but (100) features are rarely mentioned in the literature. Our observations reveal the importance of (100) as a cleavage or parting as well as the tendency in nephrites, byssolites and asbestos towards a lath-like (parallel to z) morphology with flattening on (100). In the latter varieties therefore, the y-direction is that of second fastest crystal growth, after z.

When subjected to moderate grinding, the comminution of asbestos fibres proceeds more by separation of fibrils and less by fracturing to shorter lengths as compared with prismatic and byssolite specimens. Prolonged grinding does, however, shorten lengths of even the least brittle asbestos.

Transmission electron microscopy revealed extensive sub-grain boundaries and dislocation networks (suggesting a deformation history) in all prismatic and nephrite specimens. Fine multiple (100) twinning was observed in asbestos but not in other varieties. Although chain-width defects [on (010)], with visibility enhanced by beam damage, were most abundant in nephrites and fibrous tremolites, there appears to be no completely consistent relationship between such features and morphological type.

Electron probe analyses showed that specimens that contain more than a very small amount of aluminium do not have asbestiform habit. Asbestos specimens also have lower contents of Mn, Na and K and have formulae closer to the ideal Ca₂(Mg,Fe)₅Si₈O₂₂(OH)₂. Small departures from this in asbestos involve Na in the A site compensated by Na for Ca rather than Al for Si whereas the reverse is true in byssolites. Chemical substitutions in prismatic specimens are much less constrained.

The characteristics of the four morphological sub-groups correlate reasonably well with what is known of their geological environments.     

Magmatic-subsolidus and oxidation trends in composition of amphiboles from silica-saturated peralkaline igneous rocks

Summary Sub-calcic alkali amphiboles from silica-saturated peralkaline rocks exhibit two main patterns of compositional variation, which we term the magmatic-subsolidus and oxidation trends. The first is a continuous change from magmatic to subsolidus amphibole from barroisite through richterite to arfvedsonite, involving substitutions under reducing conditions, mainly of the type Al^ivCaSi(Na,K). The second trend is towards riebeckite, under the influence of oxidizing hydrothermal fluids, according to a reaction such as Fe²⁺ SiFe³⁺ Al^vi or (K, Na)^A Fe²⁺Fe³⁺. Textural evidence suggests that fluid characteristics are as important as host-rock compositions in controlling the chemical characteristics of amphiboles in peralkaline intrusive and volcanic rocks.

---

Magmatische Subsolidus-und Oxydations-Trends der Zusammensetzung von Amphibolen aus Si-gesättigten peralkalinen Magmatiten

Zusammenfassung Alkali-Amphibole aus Si-gesättigten peralkalinen Gesteinen zeigen zwei definierte Trends chemischer Variation, die hier als magmatisch-subsolidus und Oxydations-Trend bezeichnet werden. Der erstere stellt einen kontinuerlichen Übergang von magmatischen zu subsolidus Amphibolen dar, und zwar von Barroisit über Richterit bis zu Arfvedsonit, wobei Substitutionen unter reduzierenden Bedingungen, hauptsächlich des Typs Al^iv CaSi(Na,K), zu beobachten sind. Der zweite Trend zeigt, unter dem Einfluß oxydierender hydrothermaler Lösungen, eine Tendenz auf Riebeckit hin, entsprechend einer Reaktion wie z.B. Fe²⁺ Si Fe³⁺ Al^vi oder (K, Na)^AFe²⁺ Fe³⁺. Mikroskopische Befunde weisen darauf hin, daß die Eigenschaften dieser Lösungen genauso wichtig für die chemische Zusammensetzung der Amphibole in peralkalinen Intrusiv-Gesteinen und Vulkaniten sind, wie die Zusammensetzung der Wirtsgesteine.

---

---

With 6 Figures     

Exsolution of Ca-amphibole from glaucophane and the miscibility gap between sodic and calcic amphiboles

Transmission and analytical electron microscopy (TEM/AEM) of glaucophane from glaucophane + Ca-amphibole-bearing blueschist and eclogite from two Vermont localities (Ecologite Brook and Tillotson Peak) and one California locality (Cazadero) has revealed the first evidence from exsolution for the miscibility gap between sodie and calcic amphiboles. The Tillotson Peak samples and the Cazadero samples contain coarsegrained glaucophane—actinolite pairs, while the Eclogite Brook samples contain coexisting glaucophane and actinolitic hornblende. Ca-rich glaucophanes contain abundant fine-scale lamellae of Ca-rich amphibole. These lamellae are usually oriented near (100) and . High-resolution TEM (HRTEM) images show them to be coherent. The exsolution lamellae are so narrow, beyond the resolution of AEM, that their true Ca contents are obscured by analytical contributions from the surrounding host. The AEM data suggest that the lamellae are either winchite or actinolite, depending on the true Ca concentration. In most cases, the exsolution lamellae have very curved interfaces and show variable orientation. This is attributed to the close similarity of unit-cell parameters for the two amphiboles. Three-dimensional optimal phase-boundary calculations using EPLAG (Fleet 1982) show that the observed 100 and orientations are consistent with the minimization of area strain between the two lattices along the interface. Some samples show evidence for incipient exsolution in the form of homogeneously distributed, fine-scale precipitates. These results suggest that Ca-rich glaucophanes from other glaucophane—actinolite assemblages may be exsolved at the TEM scale. The coexisting amphiboles from Eclogite Brook also have been studied using the electron microprobe (EMP). The compositional gap defined by the Eclogite Brook pairs is consistent with previously reported results, but shows a wider break along the glaucophane—actinolite pseudobinary join, suggesting very limited solid solution up to temper-atures of about 500–550°C. The glaucophanes are relatively poor in Ca, except for one anomalous grain containing Ca-amphibole lamellae. Ferric iron, estimated by normalization to fixed cation numbers, is strongly partitioned into the actinolitic hornblende and the glaucophanes are very poor in the riebeckite component.     

Multiple-chain and other unusual faults in amphiboles

A combination of high resolution transmission electron microscopy and computer simulation has revealed the existence of multiple-chain and other faults in nephrite jade. Attention is drawn to the subunit cell reorganization involved with many of these faults, which generally appear to be free from severe structural strain.