Chemical and stable isotope composition of the high grade metamorphic rocks from the Arendal area,Southern Norway

A group of high grade metamorphic rocks from the Arendal area in Southern Norway has been analyzed for bulk geochemistry, and carbon and sulfur isotopic composition. A good correspondence between the composition of the Arendal rocks and common unmetamorphosed sedimentary and magmatic rocks suggests that except for some volatile compounds no mass transport took place during metamorphism. The high grade mafic rocks interlayered with the metasediments originate from basaltic tuffs and/or intrusives.Carbon occurs as graphite and also in small amounts in a still unidentified form. The carbon of the silicic metasedimentary rocks is isotopically light with an average ¹³C of –20.2, but significantly heavier than carbonaceous matter from unmetamorphosed Precambrian sediments. This is probably due to thermal pyrolysis of the original sedimentary organic matter and to the escape of a gas phase enriched in light carbon by reactions with the graphitic substance during metamorphism.Both the metasediments and the high grade mafic rocks have relatively high sulfur contents. The mean ³⁴S values are 3.3 and 1.8, respectively. This can be explained by isotopically heavy sulfur in the original sediment. Some migration of sulfur probably has occurred from the metasediments into the metamafic rocks.No influence of the hypersthene isograd on the chemical and stable isotope composition could be detected.     

大别山低级变质岩的构造背景

大别山南北两侧的浅变质岩是碰撞造山以前洋壳俯冲造山阶段的重要组成部分。木兰山片岩或张八岭群是俯冲的洋壳;苏家河群、信阳群和佛子岭群是由洋壳俯冲形成的海沟沉积,并因俯冲过程中的前进变形而形成增生楔;杨山煤系和梅山群是石炭纪弧前盆地沉积,并因俯冲过程中的前进变形而被增生楔逆掩。宿松群是扬子大陆被动边缘沉积,不是俯冲造山带的成员。因洋壳俯冲形成的弧和弧后盆地可能已被新生界沉积物掩盖。高压—超高压变质带是碰撞造山后期从深部折返的外来体。高压—超高压变质带正好处于洋壳和增生楔之间,破坏了早期洋壳俯冲造山带的完整性,使得洋壳俯冲造山阶段的特征被破坏,因而不易辨别。俯冲造山阶段应为奥陶纪到泥盆纪,碰撞造山阶段应从二叠纪开始。     

大别山低级变质岩的构造背景

大别山南北两侧的浅变质岩是碰撞造山以前洋壳俯冲造山阶段的重要组成部分。木兰山片岩或张八岭群是俯冲的洋壳;苏家河群、信阳群和佛子岭群是由洋壳俯冲形成的海沟沉积,并因俯冲过程中的前进变形而形成增生楔;杨山煤系和梅山群是石炭纪弧前盆地沉积,并因俯冲过程中的前进变形而被增生楔逆掩。宿松群是扬子大陆被动边缘沉积,不是俯冲造山带的成员。因洋壳俯冲形成的弧和弧后盆地可能已被新生界沉积物掩盖。高压—超高压变质带是碰撞造山后期从深部折返的外来体。高压—超高压变质带正好处于洋壳和增生楔之间,破坏了早期洋壳俯冲造山带的完整性,使得洋壳俯冲造山阶段的特征被破坏,因而不易辨别。俯冲造山阶段应为奥陶纪到泥盆纪,碰撞造山阶段应从二叠纪开始。     

Crystal chemistry and reaction relations of piemontites and thulites from highly oxidized low grade metamorphic rocks at Vitali,Andros Island,Greece

Piemontite- and thulite-bearing assemblages from highly oxidized metapelitic and metacalcareous schists associated with braunite quartzites at Vitali, Andros island, Greece, were chemically investigated. The Mn-rich metasediments are intercalated in a series of metapelitic quartzose schists, marbles, and basic metavolcanites which were affected by a regional metamorphism of the highP/T type (T=400–500° C,P>9 kb) and a later Barrovian-type greenschist metamorphism (T=400–500° C,P～-5–6 kb). Texturally and chemically two generations of piemontite (I and II) can be distinguished which may show complex compositional zoning. Piemontite I coexisted at highP/T conditions with braunite, manganian phengite (alurgite), Mn³⁺-Mn²⁺-bearing Na-pyroxene (violan), carbonate, quartz, hollandite, and hematite. Zoned grains generally exhibit a decreasing Mn³⁺ and an increasing Fe³⁺ and Al content towards the rim. Chemical compositions of piemontite I range from 2.0 to 32.1 mole % Mn³⁺, 0 to 25.6 mole % Fe³⁺, and 60.2 to 81.2 mole % Al. Up to 12.5 mole % Ca on the A(2) site can be substituted by Sr. Piemontites formed in contact or close to braunite (±hematite) attained maximum (Mn³⁺+Fe³⁺)Al_?1 substitution corrresponding to about 33 mole % Mn³⁺+Fe³⁺ in lowiron compositions and up to about 39 mole % Mn³⁺+ Fe³⁺ at intermediate Fe³⁺/(Fe³⁺+Mn³⁺) ratios. Piemontite II which discontinuously overgrows piemontite I or occurs as separate grains may have been formed by greenschist facies decomposition of manganian Na-pyroxenes according to the reaction: (1) $$\begin{gathered} {\text{Mn}}^{{\text{3 + }}} - Mn^{2 + } - bearing omphacite/chloromelanite \hfill \\ + CO_2 + H_2 O + HCl \pm hermatite \hfill \\ = piemontite + tremolite + albite + chlorite \hfill \\ + calcite + quartz + NaCl \pm O_2 . \hfill \\ \end{gathered} $$ Thulites crystallized in coexistence with Al-rich piemontite II. All thulites analysed are low-Fe³⁺ manganian orthozoisites with Mn^tot～-Mn³⁺ substituting for Al on the M(3) site. Their compositions range from 2.9 to 7.2 mole % Mn³⁺, 0 to 1.2 mole % Fe³⁺, and 91.8 to 96.7 mole % Al. Piemontites II in thulite-bearing assemblages range from 5.8 to 15.9 mole % Mn³⁺, 0 to 3.7 mole % Fe³⁺, and 83.7 to 93.6 mole % Al. By contrast, piemontites II in thulite-free assemblages are similarly enriched in Mn³⁺ + Fe³⁺ — and partially in Sr²⁺ — as core compositions of piemontite I (21.1 to 29.6 mole % Mn³⁺, 2.0 to 16.5 mole % Fe³⁺, 60.6 to 68.4 mole % Al, 0 to 29.4 mole % Sr in the A(2) site). The analytical data presented in this paper document for the first time a continuous low-Fe³⁺ piemontite solid solution series from 5.8 to 32.1 mole % Mn³⁺. Aluminous piemontite II is enriched by about 3 mole % Mn³⁺+Fe³⁺ relative to coexisting thulite in Fe³⁺-poor samples and by about 6 mole % Mn³⁺+Fe³⁺ in more Fe³⁺-rich samples. Mineral pairs from different samples form a continuous compositional loop. Compositional shift of mineral pairs is attributed to the effect of a variable fluid composition at constantP _fluid andT on the continuous reaction: (2) $$\begin{gathered} piemontite + CO_2 \hfill \\ = thulite + calcite + quartz \hfill \\ + Mn^{2 + } Ca_{ - 1} [calcite] + H{_2} O + O{_2} \hfill \\ \end{gathered} $$ Further evidence for a variable \(x_{H_2 O} \) and/or \(f_{O_2 } \) possibly resulting from fluid infiltration and local buffering during the greenschist metamorphism is derived from the local decomposition of piemontite, braunite, and rutile to form spessartine, calcite, titanite, and hematite by the reactions: (3) $$\begin{gathered} piemontite + braunite + CO_2 \hfill \\ = sperssartine + calcite + quartz \pm hermatite \hfill \\ + H{_2} O + O{_2} \hfill \\ \end{gathered} $$ and more rarely: (4) $$\begin{gathered} piemontite + quartz + rutile + braunite \hfill \\ = spessartine + titanite + hematite + H{_2} O + O{_2} . \hfill \\ \end{gathered} $$      

Phase equilibria among pumpellyite,lawsonite, epidote and associated minerals in low grade metamorphic rocks

Phase relations of pumpellyite, epidote, lawsonite, CaCO₃, paragonite, actinolite, crossite and iron oxide are analysed on an Al-Ca-Fe³⁺ diagram in which all minerals are projected from quartz, albite or Jadeite, chlorite and fluid. Fe²⁺ and Mg are treated as a single component because variation in Fe²⁺/Mg has little effect on the stability of phases on the diagram. Comparison of assemblages in the Franciscan, Shuksan, Sanbagawa, New Caledonia, Southern Italian, and Otago metamorphic terranes reveals several reactions, useful for construction of a petrogenetic grid:

1. lawsonite+crossite + paragonite = epidote+chlorite + albite + quartz + H₂O
2. lawsonite + crossite = pumpellyite + epidote + chlorite + albite+ quartz + H₂O
3. crossite + pumpellyite + quartz = epidote + actinolite + albite + chlorite + H₂O
4. crossite + epidote + quartz = actinolite + hematite + albite + chlorite + H₂O
5. calcite + epidote + chlorite + quartz = pumpellyite + actinolite + H₂O + CO₂
6. pumpellyite + chlorite + quartz = epidote + actinolite + H₂O

     

Dolomitic marbles from the ultrahigh-pressure metamorphic Kimi complex in Rhodope, N.E. Greece

Summary Dolomitic marbles from the Organi and Pandrosos areas of the ultrahigh-pressure (UHP) metamorphic Kimi complex in East Rhodope, N.E. Greece have the mineral assemblage: Cal + Dol + Ol + Phl ± Di ± Hbl ± Spl ± Ti–Chu + retrograde Srp and Chl. Several generations of calcite and dolomite with variable composition and texture represent different stages of the P–T evolution: The first stage is represented by matrix dolomite ( = 0.48) and relic domains of homogenous composition in matrix calcite ( = 0.11–0.13); the second stage is evident from precipitation of lath-shaped and vermicular dolomite in matrix calcite. The third stage is represented by veinlets of almost pure CaCO₃ and domainal replacement of prior calcite by nearly pure CaCO₃ + Ca-rich dolomite ( = 0.34–0.43). Matrix dolomite adjacent to CaCO₃ veinlets also becomes Ca-rich ( = 0.42). In fact, Ca-rich dolomites with in the range of 0.40–0.34 are reported for the first time from metamorphic marbles. Coexisting Ca-rich dolomite and Mg-poor calcite cannot be explained by the calcite-dolomite miscibility gap. This assemblage rather suggests that Mg-poor calcite was aragonite originally, which formed together with Ca-rich dolomite according to the reaction Mg–Cal → Arg + Dol (1) at ultrahigh pressures and temperatures above at least 850 °C, when dolomite becomes disordered and incorporates more Ca than coexisting aragonite does in terms of Mg. The simplest explanation of these observations probably is to suggest two metamorphic events: The first one represented by relic matrix carbonates at relatively low to moderate pressures and temperatures of ca. 750 °C, and the second one limited by the minimum temperatures for dolomite disorder (ca. 850 °C) and in the aragonite + dolomite stability field, i.e. at a minimum pressure of 3 GPa and, if the presence of diamond-bearing metapelites nearby is considered, at conditions of at least 850 °C and 4.3 GPa in the diamond stability field. As there is hardly any back-reaction of Ca-rich dolomite + Mg-poor calcite to Mg-rich calcite, peak temperatures remained below the reaction (1) and the exhumation path probably crossed the aragonite-calcite transition at much lower than peak temperature. Cooling and decompression must have both occurred extremely fast in order for the μm-sized Ca-rich dolomite textures to be preserved. An alternative explanation of the formation of “UHP”-textures and compositions is by a fluid influx that not only caused serpentinisation and chloritisation of silicates but also Mg-leaching from carbonates, particularly from Mg-rich calcite and its fine grained dolomite-precipitates, thus transforming them into Mg-poor calcite + Ca-rich dolomite.     

Corundum- and zoisite-bearing marbles in the Rhodope Zone,Xanthi Area (N. Greece): Estimation of the fluid phase pomposition

Summary In the area of Xanthi, N. Greece, regionally metamorphosed marbles which belong to the Upper Tectonic Unit of the Rhodope Zone occur as intercalations within gneisses and amphibolites. In one marble horizon abundant Al-rich minerals like corundum (ruby), spinel, Al-rich pargasite, zoisite, and anorthite were found. In some cases, spinel occurs as a rim around corundum and was formed as a reaction product of corundum + dolomite. Zoisite often coexists in equilibrium with anorthite and calcite. These relationships permit the calculation of the fluid phase composition which is found to be relatively poor in CO₂, thus indicating that abundant water was available-at least on a local scale-during the last, Barrow-type metamorphism. This water was probably supplied from the metapelites by dehydration reactions during the amphibolite facies overprint and invaded the rocks through fractures and shear zones and along the contacts between different rock types.

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Korund- und zoisit führende Marmore der Rhodope-Zone, Xanthi Gebiet (N-Griechenland): bestimmung der zusammensetzung der fluiden phase

Zusammenfassung Regionalmetamorphe Marmore, die zur oberen tektonischen Einheit der Rhodope-Zone gehören, kommen in der Xanthi-Region (N-Griechenland) als Einschaltungen in Gneisen und Amphiboliten vor. In einem dieser Marmorhorizonte konnten Al-reiche Minerale, wie Korund (Rubin), Spinell, Al-reicher Pargasit, Zoisit und Anorthit, gefunden werden. Spinell tritt bisweilen als Rand um den Korund auf, was auf eine Entstehung als Reaktionsprodukt von Korund + Dolomit hinweist. Zoisit koexistiert meist mit Anorthit und Calcit. Diese Paragenesen erlauben eine Abschätzung der Zusammensetzung der fluiden Phase: sie ist relativ arm an CO₂. Dies weist darauf hin, daß, zumindest lokal, während der Barrow-Metamorphose genügend Wasser verfügbar gewesen ist. Das Wasser stammt vermutlich aus Metapeliten, aus denen es durch Dehydrationsreaktionen während der amphibolitfaziellen Überpr:agung ausgepreßt wurde. Entlang von Bruch- und Scherzonen, bzw. an Kontakten unterschiedlicher Gesteinstypen, ist das Wasser in die betreffenden Gesteine eingewandert.

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With 3 Figures     

包含变质岩分类三要素的主要变质岩分类表

变质岩分类的三要素是:变质岩的物质成分(化学成分、矿物成分)、变质岩的组构(结构、构造)和变质岩的成因(变质作用类型和形成变质岩的物理化学条件).由于变质岩的化学成分、矿物成分、组构特征和形成变质岩的地质环境十分复杂,致使至今尚无以变质岩分类三要素为基础的、内容比较完善的分类方案.本文中主要变质岩的分类是以其分类三要素为基础编制的,首次将不同成因的变质岩类并列于同一表中、将鉴定变质岩的主要标志性矿物成分和组构特征列入同一分类表中.该分类对鉴定变质岩石具有可操作性和实用性,分类表中涵盖了自然界主要的变质岩石.     

P-T estimates and timing of the sapphirine-bearing metamorphic overprint in kyanite eclogites from Central Rhodope, northern Greece

Sapphirine-bearing symplectites that replace kyanite in eclogites from the Greek Rhodope Massif have previously been attributed to a high-pressure granulite-facies metamorphic event that overprinted the eclogitic peak metamorphic assemblage. The eclogitic mineralogy consisted of garnet, omphacitic pyroxene, rutile and kyanite and is largely replaced by low-pressure minerals. Omphacite was initially replaced by symplectites of diopside and plagioclase that were subsequently replaced by symplectites of amphibole and plagioclase. Garnet reacted during decompression to form a corona of plagioclase, amphibole and magnetite. Rutile was partly transformed to ilmenite and kyanite decomposed to produce a high-variance mineral assemblage of symplectitic spinel, sapphirine, plagioclase and corundum. The presence of quartz and corundum in the kyanite eclogites is evidence for the absence of bulk equilibrium and obviates a conventional analysis of phase equilibria based on the bulk-rock composition. To circumvent this difficulty we systematically explored the pressure-temperature-composition (P-T-X) space of a thermodynamic model for the symplectites in order to establish the pressure-temperature (P-T) conditions at which the symplectites were formed after kyanite. This analysis combined with conventional thermometry indicates that the symplectites were formed at amphibolite-facies conditions. The resulting upper-pressure limit (～0.7 GPa) of the sapphirine-producing metamorphic overprint is roughly half the former estimate for the lower pressure limit of the symplectite forming metamorphic event. Temperature was constrained (T ～ 720°C) using garnet-amphibole mineral thermometry. The P-T conditions inferred here are consistent with thermobarometry from other lithologies in the Rhodope Massif, which show no evidence of granulite-facies metamorphism. Regional geological arguments and ion-probe (SHRIMP) zircon dating place the post-eclogite-facies metamorphic evolution in Eocene times.     

Chemical mineralogy and illite crystallinity in low grade metasediments,Zarouchla Group,northern Peloponnesus,Greece

Summary Low grade metasediments from the Zarouchla Group of the Phyllite-Quartzite series in northern Peloponnesus have been investigated. Mineralogically, there is a clear distinction between the lowermost and the overlying formations. Rocks of the former contain characteristic minerals such as chloritoid or garnet whereas the other formations contain the assemblage muscovite + chlorite + qz ± paragonite ± paragonite/muscovite. Illite crystallinity values are low to middle anchizone in the uppermost formation and increase progressively through upper anchizone values in the intermediate formations, reaching low epizone values in the lowermost formation. Pumpellyite-actinolite facies metabasic rocks are sandwiched between metaclastites with upper anchizone or anchizone-epizone illite crystallinity values; and chloritoid bearing quartzites with low epizone illite crystallinity values. Although geothermometric data obtained from metasediments of the lowermost formation do not support a simple burial-related pattern of metamorphism, illite crystallinity data point to a progressive increase in metamorphic grade with stratigraphic depth.

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Chemische Mineralogie und Illitkristallinität in niedriggradigen Metasedimenten, Zarouchla, Gruppe, nördlicher Peleponnes, Griechenland

Zusammenfassung In Metasedimenten niedrigen Metamorphosegrades aus der Zarouchla Gruppe der Phyllit-Quarzit-Serien im nördlichen Peleponnes bestehen klare mineralogische Unterschiede zwischen der tiefsten und den darüber-liegenden Formationen. Gesteine der ersteren enthalten als charakteristische Minerale Chloritoid oder Granat, während die darüberliegenden Formationen weithin durch die Paragenese Muskovit + Chlorit + Quarz + Paragonit + Paragonit/Muskovit gekennzeichnet werden. Die Werte der Illit-Kristallinität entsprechen in der obersten Formation der unteren bis mittleren Anchizone und nehmen graduell zu: Werte der oberen Anchizone wurden in den dazwischenliegenden Formationen registriert um schließlich Werte der unteren Epizone zu erreichen. Metabasite in Pumpellyit-Aktinolith-Fazies treten zwischen Metaklastiten mit Illit-Kristallinitätwerten der oberen Anchizone oder des Bereiches Anchizone-Epizone und chloritoid-führenden Quarziten mit Illit-Kristallinität der niedrigen Epizone auf. Obwohl geothermometrische Daten, die von Metasedimenten der untersten Formation gewonnen wurden nicht ein einfaches Schema der Überlagerungs-Metamorphose unterstützen, weist die Illit-Kristallinität doch auf eine progressive Zunahme des metamorphen Grades mit stratigraphischer Tiefe hin.

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With 6 Figures     

The stability of osumilite in high grade metamorphic rocks

Osumilite, approximate composition K(Mg,Fe)₂ Al₅Si₁₀O₃₀, has been reported recently from two granulite localities. The mineral has been synthesised in a model pelitic composition at 1000 and 1100 ° C and 3.6–6.3 kb under conditions of low water and oxygen fugacity. Osumilite coexists, apparently stably, with hypersthene, cordierite and quartz (?) thus duplicating the mineral assemblage of one of the natural occurrences. Osumilite is in a divariant reaction relationship with cordierite and hypersthene i.e. osumilite ? cordierite + hypersthene + orthoclase+quartz. This reaction runs to the right with increasing pressure. Experimental data and field observations suggest that the joins osumilite-garnet and osumilite-sillimanite are not stable. It is suggested osumilite is involved in an invariant point in the system K₂O-MgO-FeO-A1₂O₃-SiO₂ with the phases cordierite, hypersthene, sapphirine, spinel, orthoclase and quartz. The invariant point should occur at 1000 ± 100 °C and 7± 2kb.     

Chemical composition of biotite in the metamorphic and granitic rocks of Richughuta,district Palamau,Bihar (India)

Partial chemical analyses of eighteen biotite samples along with complete analyses of the respective host rocks were carried out on some metamorphic and granitic rocks of the area around Richughuta in the Palamau district of Bihar. Chemical changes in the biotites show an increase of Ti, Fe, Mn and alkali contents with decrease of Al, Mg and MgO/FeO ratio from schist to granite. The ratio MgO/FeO increases with increase in the oxidation ratio of the host rock.     

Distribution of elements between coexisting phengite and chlorite from low grade rocks from Skiros Island,Greece

Summary The distribution of Fe²⁺ and Mg between coexisting phengite and chlorite has been examined in a suite of low-grade rocks. The distribution coefficientK _D(Mg) is influenced in part by the content of tetrahedral or octahedral Al of either chlorite or phengite and in part byX _Mg of phengite. The tie lines for the mineral pairs on a SAF triangular diagram show a subparallel trend.

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Elementarverteilung zwischen koexistierenden Phengit und Chlorit aus niedrig metamorphen Gesteinen von der Insel Skiros, Griechenland

Zusammenfassung Es wird untersucht, wie Fe²⁺ und Mg zwischen koexistierenden Phengit und Chlorit aus einer Folge schwach metamorpher Gesteine verteilt sind. Der VerteilungskoeffizientK _D(Mg) wird teils durch den Gehalt an tetraedrischem bzw. oktaedrischem Al in Chlorit oder in Phengit und teils durch dasX _Mg vom Phengit beeinflußt. Die Konoden zwischen den Mineralpaaren in einem SAF-Dreieckdiagramm zeigen subparallelen Verlauf.

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With 4 Figures     

Preliminary note on deerite from high-pressure metamorphic rocks of Sifnos,Greece

A new occurrence of deerite-bearing quartzites from blueschist metamorphic rocks of the Greek island of Sifnos is described, and analytical and X-ray data on deerite are presented.     

High-pressure metamorphism in gneisses and pelitic schists in the East Rhodope zone (N. Greece)

Summary The high-alumina metapelites and the orthogneisses of the lower tectonic unit of East Rhodope underwent high P/T metamorphism followed by partial reequilibration during decompression under epidote-amphibolite/amphibolite facies to greenschist facies conditions. The high P/T mineral paragenesis in the orthogneisses is: quartz + albite + microcline + phengite (Si_max = 7 atoms p.f.u.) + biotite and in the high alumina metapelites: garnet + chloritoid + chlorite + phengite (Si_max. = 6.85 atoms p.f u.) + paragonite + quartz. Pressures between 14 and 15.5 kbar, for T_min = 550°C, are estimated for the high P/T metamorphism. During continuing uplift, staurolite + chlorite, staurolite + biotite and finally andalusite + Fe-ripidolite are grown at the expense of chloritoid in metapelites, while in the orthogneisses oligoclase, still coexisting with albite, is formed; in both rock types the Si content of white K-mica decreases considerably from almost pure phengite to pure muscovite.

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Hochdruck-Metamorphose in Gneisen und pelitischen Schiefern der östlichen RhodopeZone, Nord-Griechenland

Zusammenfassung Die Aluminium-reichen Metapelite und die Orthogneise der unteren tektonischen Einheit der östlichen Rhodope-Zone wurde unter hohen Drucken und Temperaturen metamorphosiert. Darauf folgte eine teilweise Reequilibration unter Druck-Entlastung bei Bedingungen der Epidot-Amphibolit/Amphibolit bis Grünschiefer Fazies. Die Hoch-P/T Mineral-Assoziation in den Orthogneisen besteht aus: Quarz + Albit + Mikroklin + Phengit (Si_max = 7 atoms p.f.u.) + Biotit und in den Aluminium-reichen Metapeliten: Granat + Chloritoid + Chlorit + Phengit (Si_max = 6.85 atoms p.f.u.) + Paragonit + Quarz. Drucke zwischen 14 and 15.5 kbar für T_min = 550°C wurden für die Hoch- P/T Metamorphose berechnet. Während andauernder Anhebung bildeten sich Staurolit + Chlorit, Staurolit + Biotit und schließlich Andalusit + Fe-Ripidolit auf Kosten von Chloritoid in den Metapeliten, während in den Orthogneisen Oligoklas der noch mit Albit koexistiert, gebildet wurde; in beiden Gesteinstypen nimmt der Si-Gehalt heller Kaliglimmer von fast reinem Phengit bis zu reinem Muskowit ab.

     

Cymrite and celsian in manganese-rich metamorphic rocks from Andros Island/Greece

Manganese-rich rocks from the island of Andros (Cyclades/Greece) contain cymrite (BaAl₂Si₂O₈·H₂O) and celsian. The textural relationships indicate replacement of celsian by cymrite. Several microprobe analyses of cymrites show a solid solution of 0.7–6.1 mole% KAlSi₃O₈·H₂O. The relic celsians have similar K contents. Thus the described rocks from Andros represent the first natural example for the reaction celsian+water= cymrite. The rocks from Andros underwent an Eocene high pressure metamorphism. Lateron, the high pressure parageneses were nearly effaced by a Late Oligocene Barrovian type metamorphism. It is assumed that both cymrite and celsian were formed at conditions near the reaction curve celsian_ss+water= cymrite_ss during the Barrovian type event.     

Paleozoic rocks in infrastructure of the metamorphic core, the Greater Caucasus Main Range zone

Granitoid orthogneisses and migmatites are widespread in the lower, deeply metamorphosed gneiss-migmatite complex of the pre-Alpine basement (infrastructure) exposed within northern part of the Greater Caucasus Main Range zone. Like the other rocks of the complex, they have been traditionally attributed to the Proterozoic, but the U-Pb dating revealed the Late Paleozoic age of migmatites and Devonian age of orthogneiss protolith. Bodies of blastomylonitic apogranite gneisses, which are confined to boundary between gneiss-migmatite complex and overlying Makera Complex of supracrustal rocks, turned out to be of the Late Paleozoic age as well. The dating results suggest synchronism and, apparently, genetic interrelations between the high-T/low-P metamorphism and granite formation in the Main Range zone of the Greater Caucasus.