冀东太平寨地区麻粒岩及有关岩石的辉石研究

冀东早太古代迁西群是由火山-沉积岩系变质生成的一套变质杂岩。它的主体是麻粒岩类以及退变质生成的斜长角闪岩类的岩石。该套变质岩系的下部夹有层状和透镜状变质超镁铁质岩(变橄辉岩、变辉橄岩、变辉石岩及变闪辉岩),而上部为变质的含铁岩系。以石渣子山和娄子山为例,它们的含铁岩层分别为辉石磁铁石英岩和英榴易熔岩。 本区的麻粒岩和斜长角闪岩在岩相学上呈渐变关系。绝对不含角闪石和/或富钛黑云母的麻粒岩是很少的。本文将以角闪石和斜长石为主要组成矿物的岩石归为斜长角闪岩类。在斜长角闪岩类岩石中,角闪石含量大大超过辉石,另外常见被角闪石交代的辉石残晶。     

A statistical-chemical and thermodynamic approach to the study of lunar mineralogy

Principal components analysis is used to study the chemical compositions of pyroxenes of five Apollo 12 specimens. Important correlations recognized in the variation of oxide weight per cent are: MGO, Al₂O₃, SiO₂| CaO, TiO₂, FeO MgO, Al₂O₃, SiO₂| FeO MgO, SiO₂, FeO | Al₂O₃, CaO, TiO₂ where the oxides on one side of the bar are correlated positively with each other and negatively with the oxides on the other side. Several other similarly distinct relationships with significantly less variance could be noted. These correlations indicating substitutional relationships can be interpreted as representative of stable and metastable trends of crystallization by using crystal-chemical and thermodynamic information. The per cent variance of pyroxene groups with characteristic trends in each specimen can be evaluated and interpreted in terms of history of crystallization. Distribution of Fe and Mg in certain pairs of olivine and pyroxene, which are found in contact in the rock and which may have crystallized simultaneously, is useful in recognizing the tendency towards chemical equilibrium in FeMg distribution during a limited interval in the liquidus or subsolidus stages.     

Acebuches amphibolites in the Aracena hercynian metamorphic belt (southwest Spain): Geochemical variations and basaltic affinities

A 1500–2000 m sequence of amphibolites exhibits progressively increasing metamorphic grade from greenschist to the amphibolite/granulite facies transition. The chemical variations are considered to be principally inherited from the basaltic parent. The appearance of clinopyroxene is related to P,T and to bulk-rock composition during metamorphism. Excluding some basal rocks in the orthopyroxene zone, chemical variations related to metamorphism are minor. The small decrease in the K₂O content from 0.3% to 0.1% with increasing grade suggests that the low K content was a characteristic of the basaltic precursor. These amphibolites have affinities with abyssal tholeiites.     

Phase relations of pyroxene and amphibole in greenstone,blueschist and eclogite of the Franciscan Complex,California

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.     

Mg,Fe2+ site occupancies in coexisting pyroxenes

The separate distributions for MgSiO₃ and FeSiO₃ in coexisting pyroxenes from the Skaergaard and Bushveld intrusions and charnockites, which were introduced in an earlier communication, indicate directly that significant amounts of both Fe²⁺ and Mg were present in the M(2) site of the Ca-rich pyroxene at the temperature of final intercrystalline equilibration. The calculated Fe²⁺ M(2) site occupancy in the Ca-rich pyroxene increases markedly with decrease in total MgSiO₃ content but the corresponding Mg site occupancy appears largely independent of MgSiO₃. The mean value of the distribution constant for intracrystalline exchange in the Ca-rich pyroxene decreases, away from unity, with decreasing temperature of equilibration. Occupancy of Mg and Fe²⁺ in the M (2) site of the Ca-rich pyroxene effectively compensates for the expected variation in K _D with composition resulting from intracrystalline partition in Ca-poor pyroxene, and this largely accounts for the difference in K _D between igneous and metamorphic pyroxenes. The variation of the augite limb of the pyroxene solvus within the pyroxene quadrilateral is developed as a possible geothermometer.     

集安岩群石榴石成分特征及其动力学意义

集安岩群石榴石以富铁为特征，均属铁铝榴石。形成于高角闪岩相的石榴石成分比较稳定，＜ＦｅＯ＞平均含量３２．２０％，ＭｇＯ５．１７％，Ｘ＿（Ｍｇ）平均值０．２３；结晶于低角闪岩相的石榴石（ＦｅＯ＋ＭｇＯ）含量３３．５０％，（ＭｎＯ＋ＣａＯ）６．９１％。石榴石微区成分不均匀，晶体内具有一些微区成分环带，这种环带不是各进变质作用阶段ｐ－Ｔ条件平衡或近平衡的产物。石榴石边缘存在着明显的扩散环带，表现为晶体边缘相对晶体核部，Ｃａ含量和＜ＦｃＯ＞含量增高，ＭｇＯ含量降低，Ｘ＿（Ｍｇ）值变小，反映本区变质峰期后经历的是一个近等压冷却的地质动力学过程。     

The Lac Cornu retrograded eclogites (Aiguilles Rouges massif,Western Alps,France): evidence of crustal origin and metasomatic alteration

Metabasic rocks interbedded in amphibolite facies supracrustal gneisses outcrop around Lac Carnu in the Aiguilles Rouges massif (Western Alps). The cores of the thickest boudinaged lenses are made up of eclogitic amphibolites grading outwards into amphibolites. The common assemblage is unzoned garnet + symplectitic clinopyroxebe + hornblende + plagioclase. In a slightly amphibolitized sample, minimum P and T conditions of equilibrium between garnet and omphacite inclusions are 780°C and 11 Kb. A polymetamorphic pre-Alpine evolution of the massif is thus demonstrated. Eclogitic amphibolites show variations in major element composition similar to the Skaergaard evolution in the Al₂O₃ ? FeO + Fe₂O₃ ? MgO triangle. Variation diagrams in which Zr is taken as differentiation index also indicate magmatic trends for Mn, Ti, P, Ni, Co, Y, V and Cr, Ca, K, Na, Sr, Rb and Si were mobile during the evolution of the rocks. The igneous trend can be described by a quantitative model of fractional crystallization in which a noritic assemblage separated in the initial stage. This provides evidence of crustal P, T conditions of differentiation for the original materoal and in situ evolution for the eclogites. A second group of amphibolites shows banded structure and transitional terms with the surrounding gneisses. A volcano-sedimentary origin is suggested though the process cannot be modelled. The rocks may result from complex interactions of magnetic, metasomatic and sedimentary processes. It is concluded that Lac Cornu metabasites were originally continental tholeiites, though several geochemical criteria tend to indicate an oceanic origin. This casts some doubt on the validity of these criteria, when applied to metamorphic rocks.     

Petrology of mafic inclusions from Itinome-gata,Japan

Various types of mafic inclusions up to 30 cm in size occur in lapilli tuff of alkali basalt at Itinome-gata crater, northeastern Japan. They are divided into the following four groups: amphibolite, hornblendite—hornblende gabbro, leucogabbro, and pyroxene gabbro. Also occurring with the mafic inclusions are lherzolite and websterite inclusions and megacrysts of Mg-rich olivine and chromian diopside. New analyses are presented for twenty five representative mafic inclusions, eight clinopyroxenes, six orthopyroxenes, and fifteen brown hornblendes. There are conspicuous chemical differences between the mafic inclusions and lherzolite and websterite inclusions: the former have higher TiO₂, Al₂O₃, total FeO, CaO, Na₂O, and K₂O, and lower MgO than the lherzolites and higher TiO₂, Al₂O₃, total FeO, and alkalis, and lower MgO than the websterites. The petrographic and chemical gradations among these three are not easily recognized. It is indicated that the Moho in this region is a boundary between mafic and ultramafic phases. The mineral assemblages of the mafic inclusions and the compositions of their essential minerals show that all of them recrystallized or crystallized under approximately the same temperature — pressure conditions, within the range of 600–1000° C and 6–9 kb. The following is hypothetically considered. The old and thick tholeiites or high-alumina basalts (may be pre-Silurian) making up the basement of the Japanese Islands had been subjected to the high T/P type metamorphism during Cretaceous time, and changed to amphibolites. In the cataclastic stage, complete melting of the lower part of the amphibolites occured locally and formed a gabbro magma. This gabbro magma moved upward slightly and produced hornblendite, hornblende gabbro and leucogabbro magmas by differentiation under wet conditions and a pyroxene gabbro magma under less wet conditions. Namely, the mafic inclusions are thought to be of fragments of the lower crust.     

An application of R-mode factor analysis to the study of metamorphic petrogenesis

R-mode factor analysis of modal and chemical data clarifies the trends of mineralogical evolution and associated chemical variations in amphibolites from the Northwest Adirondack Mountains, New York and the Willyama Complex, Broken Hill District. In both areas the principal mineralogical reaction attending metamorphism, as described by the first factor, appears to have been Hornblende + Quartz → Calcic pyroxene + Orthopyroxene + Plagioclase. For the Adirondack amphibolites, the derived reaction coefficients viewed against the modal contents of the pyroxenes suggest another hornblende breakdown reaction producing calcic pyroxene, which is corroborated by the first appearance of the phase a little NE of Emeryville. The other factors extracted reveal the underlying parameters responsible for the development of biotite, sphene, opaques and quartz in the Adirondack metabasites and albite, anorthite, ilmenite and quartz in the Willyama Complex amphibolites.The analysis also demonstrates that the principal mineralogical reactions in both the areas have been combinations of thermal and ionic types and further that to decipher the net mineralogical changes in high grade metamorphic basic and pelitic rocks it is necessary to extend the integration of the ‘part reactions’ occurring in different domains to the level of a hand specimen.     

Petrology and Rare Earth Elements Mineral Chemistry of Chadegan Metabasites (Sanandaj-Sirjan Zone,Iran): Evidence for Eclogite-Facies Metamorphism during Neotethyan Subduction

The metabasites of Chadegan, including eclogite, garnet amphibolite and amphibolite, are forming a part of Sanandaj–Sirjan Zone. These rocks have formed during the subduction of the Neo–Tethys ocean crust under Iranian plate. This subduction resulted in a subduction metamorphism under high pressuremedium temperature of eclogite and amphibolites facies condition. Then the metamorphic rocks were exhumed during the continental collision between the Afro–Arabian continent and the Iranian microcontinent. In the metabasite rocks, with typical MORB composition, garnet preserved a compositional zoning occurred during metamorphism. The magnesium (X_Mg) gradually increases from core to rim of garnets, while the manganese (X_Mn) decreases towards the rim. Chondrite–normalized Rare Earth Element patterns for these garnets exhibit core–to–rim increases in Light Rare Earth Elements. The chondrite–normalized REE patterns of garnets, amphiboles and pyroxenes display positive trend from LREEs to Heavy Rare Earth Elements (especially in garnet), which suggests the role of these minerals as the major controller of HREE distribution. The geochemical features show that the studied eclogite and associated rocks have a MORB origin, and probably formed in a deep–seated subduction channel environment. The geothermometry estimation yields average pressure of ~22 kbar and temperature of 470–520°C for eclogite fomation. The thermobarometry results gave T = 650–700°C and P ≈ 10–11 kbar for amphibolite facies.     

Geochemistry and palaeotectonic setting of amphibolites from the Western Tatra Mountains,southern Poland

Amphibolites from the crystalline basement of the Western Tatra Mountains, which are found as small lenses within migmatitic gneisses and mica schists, were formed during pre‐ or early Variscan amphibolite‐facies metamorphic events, and subsequently intruded by the post‐metamorphic Variscan Tatra Granite. The amphibolites occur in both the upper and lower metamorphic complexes, which are separated by a major subhorizontal shear zone in the Western Tatra Mountains. The amphibolites can be divided into three types: massive, striped and garnetiferous. The striped and massive amphibolites, concordant with a dominant S₁ foliation, and the garnet amphibolites, which cross‐cut the S₁ banding in the gneisses, were all originally intrusive dolerites. The striped amphibolites (consisting primarily of hornblende, andesine and quartz), and later, cross‐cutting garnet‐hornblende‐andesine‐quartz‐bearing amphibolites, predominate in the lower part of the dominantly migmatitic upper complex, and are exposed mainly on the ridges. The massive amphibolites, which contain a similar mineral assemblage, mainly occur in the usual unmigmatized lower structural unit. Chemical studies indicate that three amphibolite suites are present, which probably originated as a series of enriched tholeiites, similar to more recent plume‐influenced magmas, which were derived by partial melting of a spinel lherzolite with primitive mantle composition and compositionally slightly modified by crustal contamination. The amphibolites were intruded as dolerites into clastic sediments which had accumulated in an extensional basin floored by attenuated continental crust, a situation similar to that of amphibolites found in metamorphic complexes within the Variscan belt, e.g. in the Orlica–Snieznik area of the Sudetes, where amphibolites chemically similar to those in the Western Tatra also occur. Copyright © 2000 John Wiley & Sons, Ltd.     

Evolution of pyroxene in peralkaline magmatic system: An example of an agpaitic syenite dyke complex and the Niva intrusion,Kola Peninsula

The paper presents pioneering data on the composition of pyroxenes and the distribution of trace elements in this mineral in small geological bodies that were formed by single magma injections and their subsequent rapid crystallization: the Niva intrusion and an agpaitic syenite dyke. The pyroxene is highly alkaline and shows continuous compositional trends with an increase in the aegirine concentration. The Ti concentrations of the pyroxene are much higher than in pyroxenes in agpaitic syenites in other alkaline complexes. In spite of the fact that the pyroxene is hosted in small bodies, the evolution of these pyroxenes was similar to that of pyroxenes in the Lovozero and Khibina alkaline massifs.     

Compositional evolution in Ca-amphibole in the Karmutsen metabasites, Vancouver Island, British Columbia, Canada

Abstract The 6-km-thick Karmutsen metabasites, exposed over much of Vancouver Island, were thermally metamorphosed by intrusions of Jurassic granodiorite and granite. Observations of about 800 thin sections from the Campbell River and Buttle Lake area show that the metabasites provide a complete succession of mineral assemblages ranging from the zeolite to pyroxene hornfels facies around the intrusion. The most important observations are as follows. (1) The compositional change of Ca-amphiboles with increasing metamorphic grade is not straightforward. The tremolite component decreases from the prehnite–actinolite facies to the greenschist facies with a compensating tschermak component increase, but the tendency is not clear thereafter. Instead, the edenite component increases from the amphibolite facies to the pyroxene hornfels facies. (2) The most pargasitic Ca-amphibole occurs in high-Fe²⁺/Mg metabasite from the greenschist/amphibolite transition zone. (3) The reasons for such irregular compositional trends, even in the rather uniform MORB-like composition of the Karmutsen metabasites, are non-ideal solid solutions of Ca-amphibole at low temperature and the effective control by bulk rock composition in the amphibolite facies. (4) The data from this study support, but do not prove, a transition loop for the actinolite–hornblende compositional gap rather than a solvus. If the gap is a solvus, its shape is asymmetric, and is highly dependent on the other compositional parameters such as Fe³⁺/Al and Fe²⁺/Mg. (5) The X_NaA/X_A±X_Ab) ratios between Ca-amphibole and plagioclase are most useful as an indicator of metamorphic grade even within the amphibolite facies, and these change systematically from 0.2 to 0.5 from the greenschist to pyroxene hornfels facies. (6) The compositional trend of Ca-amphibole from the Karmutsen metabasites indicates a typical low-P/T metamorphic facies series on a Rbk–Gln–Tr–Ts diagram.     

Geochemistry and tectonic significance of metamorphic sole rocks beneath the Beyşehir–Hoyran ophiolite (SW-Turkey)

The Beyşehir–Hoyran ophiolite is situated in the western part of the Tauride belt (SW Turkey) and crops out at two localities north of the lake Beyşehir. It mainly comprises harzburgitic peridotites that were tectonically emplaced to their present position during the Late Eocene. The ophiolites themselves are tectonically overlain by either slope basin deposits with lava blocks (Eğirler formation) or massive Triassic limestone blocks (Deliktaş formation). High-grade sub-ophiolitic metamorphic rocks, i.e. epidote amphibolite, amphibolite, and pyroxene amphibolite, together with minor quartzite and calcschist, are observed at the base of the ophiolite sequence, where they occur as thin tectonic slices with an inverted metamorphic gradient. Average P–T conditions of 630–770 °C and c. 6 ± 1.5 kbar are calculated for the metamorphism of the amphibolites by conventional geothermobarometry, corresponding to a burial depth of 18–20 km. Both the sub-ophiolitic metamorphic rocks and the overlying mantle tectonites were intruded by isolated tholeiitic (Nb/Y = 0.041–0.108) diabase dikes, which do not transect the tectonic contact between the two units. Geochemical investigations of the amphibolites of the sub-ophiolitic rock suite show two different geochemical affinities, with the first group being alkaline in character (Nb/Y = 1–3.86) and the second one being tholeiitic (Nb/Y = 0.064–0.13). REE patterns, trace element plots and tectonomagmatic discrimination diagrams indicate that the most probable protoliths for alkaline amphibolites are within-plate type alkali basalts, whereas those of the tholeiitic group resemble tholeiitic island arc basalts. Similarities between the geochemical characteristics of the amphibolites and those of the volcanic rocks of the Eğirler formation strongly suggest that the latter are the protoliths of the amphibolites.     

Pyroxene in enclaves and syenites of the Red Hill complex,New Hampshire: an ion and electron microprobe study

The Red Hill complex, New Hampshire, contains both silica-undersaturated and silica-saturated to oversaturated syenites. Ion microprobe analyses of pyroxene from the Nepheline Sodalite Syenite (NSS) and its enclaves reveal that the REE abundances increase in a systematic manner from low values in the enclave pyroxenes to higher values in the NSS host rock pyroxenes. This variation is interpreted to have resulted from differentiation and coupled with previously published mineral and bulk-rock compositions, suggests that the enclaves represent samples of NSS parental liquids that intruded into residual, syenitic liquids in a zoned magma chamber. Pyroxene analyses of the Garland Peak Syenite (GPS) and its enclaves indicate that the enclaves are of several populations: some may be related to the GPS, others are not. The GPS itself is heterogeneous and pyroxene trace element zoning is difficult to explain by fractionation processes. The silica-oversaturated Outer Coarse Syenite (OCS) contains pyroxenes with trace element characteristics that are distinct from the NSS. The low V concentrations suggest that the OCS exprienced magnetite fractionation prior to pyroxene growth. It is proposed that high f O₂in the OCS magma caused Fe-Ti oxide crystallization, which in turn, influenced magmatic silica activity. The chondrite normalized REE patterns of OCS pyroxenes are also suggestive of titanite crystallization, another indication of high f O₂. In contrast to the influence of magnetite crystallization, the high and rimwardly increasing Y and Yb concentrations in both the NSS and the OCS pyroxenes suggest that amphibole fractionation was not the major influence on silica activity. Therefore, it is unlikely that the OCS was derived by amphibole fractionation from a NSS precursor magma.     

Metamorphic history of eclogites and country rock gneisses in the Aktyuz area,Northern Tien‐Shan,Kyrgyzstan: a record from initiation of subduction through to oceanic closure by continent–continent collision

Eclogites and related high‐P metamorphic rocks occur in the Zaili Range of the Northern Kyrgyz Tien‐Shan (Tianshan) Mountains, which are located in the south‐western segment of the Central Asian Orogenic Belt. Eclogites are preserved in the cores of garnet amphibolites and amphibolites that occur in the Aktyuz area as boudins and layers (up to 2000 m in length) within country rock gneisses. The textures and mineral chemistry of the Aktyuz eclogites, garnet amphibolites and country rock gneisses record three distinct metamorphic events (M1–M3). In the eclogites, the first MP–HT metamorphic event (M1) of amphibolite/epidote‐amphibolite facies conditions (560–650 °C, 4–10 kbar) is established from relict mineral assemblages of polyphase inclusions in the cores and mantles of garnet, i.e. Mg‐taramite + Fe‐staurolite + paragonite ± oligoclase (An_<16) ± hematite. The eclogites also record the second HP‐LT metamorphism (M2) with a prograde stage passing through epidote‐blueschist facies conditions (330–570 °C, 8–16 kbar) to peak metamorphism in the eclogite facies (550–660 °C, 21–23 kbar) and subsequent retrograde metamorphism to epidote‐amphibolite facies conditions (545–565 °C and 10–11 kbar) that defines a clockwise P–T path. thermocalc (average P–T mode) calculations and other geothermobarometers have been applied for the estimation of P–T conditions. M3 is inferred from the garnet amphibolites and country rock gneisses. Garnet amphibolites that underwent this pervasive HP–HT metamorphism after the eclogite facies equilibrium have a peak metamorphic assemblage of garnet and pargasite. The prograde and peak metamorphic conditions of the garnet amphibolites are estimated to be 600–640 °C; 11–12 kbar and 675–735 °C and 14–15 kbar, respectively. Inclusion phases in porphyroblastic plagioclase in the country rock gneisses suggest a prograde stage of the epidote‐amphibolite facies (477 °C and 10 kbar). The peak mineral assemblage of the country rock gneisses of garnet, plagioclase (An_11–16), phengite, biotite, quartz and rutile indicate 635–745 °C and 13–15 kbar. The P–T conditions estimated for the prograde, peak and retrograde stages in garnet amphibolite and country rock are similar, implying that the third metamorphic event in the garnet amphibolites was correlated with the metamorphism in the country rock gneisses. The eclogites also show evidence of the third metamorphic event with development of the prograde mineral assemblage pargasite, oligoclase and biotite after the retrograde epidote‐amphibolite facies metamorphism. The three metamorphic events occurred in distinct tectonic settings: (i) metamorphism along the hot hangingwall at the inception of subduction, (ii) subsequent subduction zone metamorphism of the oceanic plate and exhumation, and (iii) continent–continent collision and exhumation of the entire metamorphic sequences. These tectonic processes document the initial stage of closure of a palaeo‐ocean subduction to its completion by continent–continent collision.     

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.     

The garnets of the eastern area of the Sierra de Guadarrama,Sistema Central,Spain

Electron-probe microanalysis of a series of garnets in metapelitic rocks of the chloritoid staurolite, kyanite and sillimanite metamorphic zones, eastern area of the Sierra de Guadarrama, Sistema Central, Spain, manifest the well-known cryptozonation commonly observed in these minerals, with MgO and FeO increasing and MnO and CaO decreasing from the center to the outer rim of the crystals.The differences in composition of the garnets, from one metamorphic zone to another, is mainly a result of small differences in composition of the host-rock, since: (1) the amounts of MnO in the garnet are controlled by the amounts of SiO₂, Al₂O₃ and FeO present in the host-rock; and (2) the percentages of MnO and MgO of the parent-rock influence in some way the concentration of CaO in the garnet, and those of MnO, Al₂O₃ and CaO influence the concentration of FeO. Nevertheless, the amount of FeO in the garnet is finally controlled, due to the diadochy, by the concentration of MnO + CaO in this mineral.     

Contributions to the mineral chemistry of Hawaiian rocks

Phenocryst and groundmass pyroxenes in 24 rocks of the tholeiitic, alkalic, and nephelinic suites from Haleakala and West Maui volcanoes, Maui, Hawaii, were analyzed quantitatively by electron microprobe. Results and conclusions: i) Tholeiites contain augite, pigeonite, and bronzite; alkalic rocks contain salite, augite, and ferroaugite; and nephelinic rocks have salite, sometimes of Wo>50 mole %. ii) The three suites can be distinguished by Ca contents of pyroxenes: High-Ca pyroxenes of tholeiitic rocks have Wo_30–40; those of alkalic rocks have Wo_38–48; and those of the nephelinic rocks have Wo_47–51; i.e. Wo in clinopyroxene increases from tholeiitic, to alkalic, to nephelinic suites, iii). In the alkalic suite, rock types can be distinguished on the basis of clinopyroxene composition: Alkalic olivine and alkalic basalts have Wo_38–45, hawaiites and mugearites have Wo_45–48. Trachytes can be distinguished from both groups by higher Fe (Fs_22–30) and Ca contents (Wo_43–47). iv) Pyroxenes in tholeiitic rocks show higher intrarock variability (e.g. Fs₁₂Wo₄₀-Fs₃₇Wo₃₀) than those of the alkalic and nephelinic suites, v) Na₂O bulk-rock content affects Na₂O content of the precipitating high-Ca pyroxene; e.g. Na₂O in groundmass pyroxene increases from tholeiitic, to alkalic (mafic members only), to nephelinic suites; a similar relationship is present within the differentiated alkalic suite, vi) In tholeiites, changes in groundmass high-Ca pyroxene compositions are related to changes in bulk rock compositions, e.g. FeO/FeO+MgO+CaO in clinopyroxene increases as this ratio increases in the bulk rock; this is not true for alkalic and nephelinic rocks, vii) In groundmass high-Ca pyroxene, Al₂O₃, Na₂0, and TiO₂ contents increase and MnO content decreases with increasing Wo content from tholeiitic, to alkalic (mafic members only), to nephelinic suites, viii) Groundmass high-Ca pyroxenes are richer in MnO and Na₂O and poorer in Cr₂O₃ compared to coexisting phenocrysts. High-Ca pyroxene phenocrysts in nephelinic rocks and in one mugearite are depleted in SiO₂ and enriched in Al₂O₃ relative to coexisting groundmass clinopyroxene, indicating increased SiO₂ activity during crystallization. Some tholeiites show the reverse; this Si—Al relationship is not clear in other samples.     

陈蔡岩群下河图斜长角闪岩年代学、地球化学特征及其构造意义

浙江诸暨市下河图村的陈蔡岩群中出露一套斜长角闪岩,空间上与块状大理岩相伴产出。地球化学研究表明,下河图斜长角闪岩SiO_2含量为43.22%~46.56%,MgO为3.23%~7.87%,TiO_2为1.90%~2.98%,与碱性洋岛玄武岩特征类似。稀土元素总量为114.47×10~(-6)~192.39×10~(-6),(La/Yb)N为5.93~12.13,稀土元素球粒陨石标准化配分模式为轻稀土元素富集的右倾型;原始地幔标准化微量元素蛛网图表现出向上隆起的富集形态,微量元素特征表明其可能形成于洋岛构造环境,陆壳物质对其混染的可能性较小,岩石成分主要受熔融源区控制。推测下河图斜长角闪岩原岩很可能形成于靠近消减带的海山环境,来源于洋壳俯冲过程中增生的海山碎片,陈蔡岩群很可能为一套俯冲增生杂岩。LA-ICP-MS锆石U-Pb法获得斜长角闪岩变质年龄为420.6±1.8 Ma,可能代表了扬子和华夏两大地块碰撞拼合的时代。