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.     

Coarsening kinetics of the exsolution microstructure in alkali feldspar

Actinolite, hornblende and biotite coexisting in greenschist mafic metagreywackes have been analysed with the electron microprobe to obtain information on their chemical relationship during metamorphism. As in some other parts of the world, the two calcic amphiboles coexist in the greenschist facies because of a miscibility gap between them which is observed under conditions of low-pressure regional metamorphism; it is thought that the two amphiboles are in equilibrium, or at least that the actinolite participated in hornblendeforming reactions. Contact metamorphism by granitic intrusives of these metagreywackes has converted them to hornblende hornfelses with the assemblage hornblende, andesine, quartz, biotite±cummingtonite; the hornblendes of the hornfelses are found to have compositions between actinolite and hornblende of the greenschists, and frequently show fine exsolution lamellae of cummingtonite as a result of oversaturation in this component. The distribution of Fe-Mg between hornblende and biotite changes from the greenschist to the hornblende hornfels facies, and the K _D is probably dependent on Al^VI in the hornblende.     

Oceanic ridge metamorphism of the East Taiwan Ophiolite

Brecciated mafic+ultramafic plutonic rocks of the East Taiwan Ophiolite occur as detritus and slide blocks in the Pliocene Lichi Mélange. These plutonic rocks have been subjected to two stages of post-magmatic recrystallization: (I) pre-brecciation ridge-type metamorphism attended by high-grade greenschist and rare amphibolite facies physical conditions; and (II) later off-axis metamorphism under zeolite to lowest greenschist facies conditions that postdated brecciation, submarine talus accumulation and deposition of associated pelagic sediments. The effects of the earlier ridge metamorphism are the main concern of this paper. (I) Dominant antigorite together with chlorite and talc in some ultramafics suggests that these rocks recrystallized at T>350 ° C. The primary compositions of gabbroic calcic plagioclase have been modified from An 45–70 to An 13–38, and the igneous clinopyroxenes and hornblendes partly replaced by actinolite+chlorite. Stable mineral assemblages in the metagabbros are thus ∼oligoclase+actinolite+chlorite±very rare epidote+sphene, and intermediate plagioclase +actinolite+chlorite+sphene. Amphibolites are less common and consist of more calcic plagioclase (An 25–49)+hornblende. The presence of assemblages transitional between greenschist and amphibolite facies for basaltic compositions is suggestive of very low-pressure thermal metamorphism such as would be appropriate to the crustal portions of an oceanic spreading center. (II) The occurrence of vein albite+actinolite+ chlorite near the base of the brecciated plutonic sequence and vein prehnite+laumontite in the upper part suggests that the brecciated plutonic rocks were later feebly retrograded under conditions of the greenschist and zeolite facies respectively-probably some distance removed from the thermal regime of a mid-oceanic ridge. The East Taiwan Ophiolite probably represents the western termination of the Philippine Sea lithospheric plate. Portions of this oceanic crust and underlying mantle were incorporated in the Lichi Mélange of the Coastal Range of eastern Taiwan as a consequence of antithetic faulting and erosion. This process evidently accompanied east-directed underflow of the Asiatic (South China Sea) plate.     

Short life-span of the ore-forming system at the Porgera gold deposit, Papua New Guinea: laser 40Ar/39Ar dates for roscoelite, biotite, and hornblende

The Porgera gold deposit, Papua New Guinea, is associated with sodic-alkalic, hypabyssal intrusions of alkali basaltic to mugearitic composition. The intrusions were emplaced into Cretaceous mudstones and siltstones in the latest Miocene, and both igneous and sedimentary rocks are mineralized. Three types of veins occur: (1) magnetite-sulfide - Au-carbonate veins; (2) base-metal sulfide - Au-carbonate veins; and, economically most important, (3) quartz-roscoelite-Au veins and breccias. Magmatic hornblende and biotite, hydrothermal biotite from alteration selvages associated with the magnetite-sulfide - Au veins, and roscoelite were dated using the laser ⁴⁰Ar/³⁹Ar step-heating technique. Magmatic biotite yielded a date of 5.99ǂ.11 Ma (2C error; MSWD=3.7), and two samples of magmatic hornblende provided dates of 6.35ǂ.23 Ma (MSWD=1.0) and 6.3ǂ.7 Ma (MSWD=2.6). Hydrothermal biotite provided a date of 5.98ǂ.13 Ma (MSWD=2.7), and analyses of two roscoelite samples yielded dates of 5.92ǂ.09 Ma (MSWD=2.0) and 5.92ǂ.17 Ma (MSWD=2.0). The date of the magmatic biotite is interpreted to represent the age of the intrusions more accurately than the hornblende dates because small amounts of excess ⁴⁰Ar were present in the hornblende samples. The date for hydrothermal biotite is interpreted to be the age of the alteration associated with the magnetite-sulfide - Au veins (the paragenetically earliest veins), and thus reflects the age of the onset of the mineralizing activity at Porgera. Based on the two dates for roscoelite, the age of the main ore deposition event is interpreted to be 5.92ǂ.08 Ma. The apparent ages for the intrusive and the mineralizing events are thus identical within error, and suggest that the magmatic and ore-forming system at Porgera was short-lived.     

峨眉山玄武岩的辉石研究

本文研究的峨眉山玄武岩的辉石均为单斜辉石。东川碱性火山岩中以透辉石为主,显示碱性岩系辉石的特征,但相对贫 LREE、Ti 等不相容元素,结晶时的 fO₂较高;攀枝花岩带主要是透辉石质普通辉石;其他剖面和地区多为普通辉石,且具拉斑质岩系富钙辉石的成分和演化特点。攀枝花带和西岩区辉石在化学成分上比较原始,而东岩区和中岩区辉石的成分演化程度相对较高。含 Ti 的“其他”阳离子对在各岩区（带）的辉石中均限重要,暗示它们的形成与火山弧环境无关。     

High temperature alteration of Abyssal ultramafics from the Islas Orcadas Fracture Zone,South Atlantic

Ultramafic rocks dredged from the Islas Orcadas Fracture Zone, along the SW Indian Ocean Ridge (6° E and 54° S), show evidence of progressive hydration beginning at temperatures greater than 600° C (and perhaps as high as 900° C) and continuing to less than 50° C. There are two principal types of alteration present in the ultramafic rocks, both of which are the result of hydration reactions. The first type of alteration involves hydration of original clinopyroxene, orthopyroxene and olivine to amphibole, talc, secondary olivine, and serpentine. The second is a vein type of alteration and results in the formation of veins of amphibole, chlorite, talc and serpentine. — The alteration appears to be episodic. The sequence of events suggested by the petrography is: 1) clinopyroxene altering to amphibole; 2) orthopyroxene altering to talc, or talc + olivine; 3) supersolvus hornblende veining; 4) coexisting actinolite + hornblende veining; 5) chlorite, chlorite + actinolite, or chlorite + secondary clinopyroxene veining; 6) talc veining; 7) serpentine veining; and 8) pervasive serpentinization. — The alteration fluid is most likely seawater. It is suggested that the high temperature alterations may reflect seawater circulation into the upper mantle.     

TEM and FESEM characterization of asbestiform and non-asbestiform actinolite fibers in hydrothermally altered dolerites (France)

This paper provides new mineralogical and morphological characterizations of calcic amphiboles from hydrothermally altered dolerites from France to discuss their potential to contain naturally occurring asbestos (NOA) and to release elongated mineral particles corresponding to asbestos fibers, or asbestos-like fibers, into the air. The calcic amphiboles were characterized using electron microprobe analysis, scanning and transmission electron microscopy. The results underline that fibrous occurrences of actinolite and ferro-actinolite regularly occur in hydrothermally altered dolerites, both in the groundmass and in quartz veins. In the groundmass, actinolitic amphiboles crystallize at the expense of magmatic clinopyroxenes and are rarely fibrous. Conversely, actinolite and ferro-actinolite fibers from quartz veins are potentially asbestiform to clearly asbestiform. The identification of quartz veins in hydrothermally altered dolerites is, therefore, an important parameter which should draw attention to the possible presence of asbestiform actinolite fibers. The mineralogical characterization of such veins as well as the estimation of their thickness and density is an important point to consider during studies involving NOA issues. Moreover, the degree of weathering of the dolerites, which directly affects the ability of non-asbestiform actinolite crystals to dissociate into very thin fibers, regarded as cleavage fragments instead of as asbestos, is also a key parameter to consider. Hydrothermally altered dolerites are common rocks likely to be exploited by the quarrying industry to produce aggregates or to be affected by construction works. Due to the abundance of actinolite fibers that they may contain locally, these rocks become priority targets to be monitored in terms of geological characterization and airborne fiber emission to ensure the protection of populations and workers.     

Petrology of the Kurancali Phlogopitic Metagabbro: An Island Arc-Type Ophiolitic Sliver in the Central Anatolian Crystalline Complex

The Kurancali metagabbro occurs as an isolated body in the central part of the Central Anatolian Crystalline Complex. It has been emplaced along a steep S-vergent thrust-plane onto the uppermost units of the Central Anatolian Metamorphics. The main body of the Kurancali metagabbro is characterized by distinct compositional layering. The layered gabbros comprise pyroxene and hornblende gabbros. Phlogopite-rich, plagioclase-hornblende gabbro occurs mainly as pegmatitic dikes intruding the layered gabbro sequence. The layered gabbros, in general, consist mainly of diopsidic augites, brown hornblendes, and plagioclase. Secondary phases are phlogopitic mica, brownish-green hornblende replacing clinopyroxenes, and fibrous, greenish actinolitic hornblende partially or completely replacing brown hornblende. The primary dark micas are phlogopitic in the range of phlogopite_(57-70) and annite_(30-43). The analyzed pyroxenes are diopsidic (En₃₂Fs₁₉Wo₄₉-En₃₅Fs₁₈Wo₄₈).

The whole-rock geochemistry of the gabbros indicates the presence of two distinct groups of rocks; a less pronounced group of phlogopite gabbro with island-arc calc-alkaline affinities, and a dominating layered gabbro sequence with island-arc tholeiite characteristics. They are extremely enriched in LILE, indicative of alkaline metasomatism in the source region, and display geochemical features of transitional backarc-basin basalts (BABB)/island-arc basalts (IAB)—and IAB-type oceanic crust. Based on their geochemical similarities to modern island-arc basements, we suggest that the Kurancali metagabbro may represent the basement of an initial island arc, generated in a suprasubduction zone setting within the Izmir-Ankara branch of Neotethys.     

Amphibolitization of metagabbros in the Scottish Highlands

Abstract Compositions of actinolite, hornblende and cummingtonite, together with pyroxene and plagioclase, are studied in basic intrusions in the Dalradian of north-east Scotland, and the Glen Scaddle complex in the West Moine. Amphibolitization is due to influx of water from the country rocks. Pyroxene compositions are found to have adjusted to the regional metamorphic environment. Owing to the difficulty of diffusion of Al and Si, calcic amphiboles are zoned and commonly contain quartz blebs. Discontinuities in zoning give rise to actinolite-hornblende pairs. Compared with north-east Scotland, disequilibrium is less strong in the Glen Scaddle area: in the latter, plagioclase compositions have been greatly changed, Na partition between hornblende and plagioclase is close to equilibrium, the maximum Al content of hornblende is lower and zoning patterns are more consistent. The Fe/Mg ratio in calcic amphiboles varies with Al content, while approaching equilibrium partition with other minerals. Both zoning patterns and Fe/Mg partition with cummingtonite suggest that Fe/Mg of the calcic amphiboles increases more strongly with increasing (Al^vi+Fe³⁺) than can be explained simply by substitution of Al,Fe³⁺ for Mg on M2. Model reactions for amphibole formation are constructed. Cummingtonite formed at lower chemical potential of CaO than actinolite: Ca was exchanged for Mg,Fe between orthopyroxene-derived and clinopyroxene-derived local systems. Both cummingtonite and actinolite were formed because of kinetic constraints, as intermediate reaction products: actinolite-hornblende pairs represent disequilibrium. This work suggests that many occurrences of actinolite with hornblende, where the minerals are zoned, may also be due to diffusion kinetics.     

Glaucophane-bearing assemblage overprinted by greenschist-facies metamorphism in the Variscan Kaczawa complex, Sudetes, Poland

An Early Palaeozoic (Ordovician ?) metamudstone sequence near Wojcieszow, Kaczawa Mts, Western Sudetes, Poland, contains numerous metabasite sills, up to 50 m thick. These subvolcanic rocks are of within-plate alkali basalt type. Primary igneous phases in the metabasites, clinopyroxene (salite) and kaersutite, are veined and partly replaced by complex metamorphic mineral assemblages. Particularly, the kaersutite is corroded and rimmed by zoned sodic, sodic–calcic and calcic amphiboles. The matrix is composed of actinolite, pycnochlorite, albite (An ≤ 0.5%), epidote (Ps 27–33), titanite, calcite, opaques and, occasionally, biotite, phengite and stilpnomelane. The sodic amphiboles are glaucophane to crossite in composition with Na^B from 1.9 to 1.6. They are rimmed successively by sodic–calcic and calcic amphiboles with compositions ranging from magnesioferri-winchite to actinolite. No compositions between Na^B= 0.92 and Na^B= 1.56 have been ascertained. The textures may be interpreted as representing a greenschist facies overprint on an earlier blueschist (or blueschist–greenschist transitional) assemblage. The presence of glaucophane and no traces of a jadeitic pyroxene + quartz association indicate pressures between 6 and 12 kbar during the high-pressure episode. Temperature is difficult to assess in this metamorphic event. The replacement of glaucophane by actinolite + chlorite + albite, with associated epidote, allows restriction of the upper pressure limit of the greenschist recrystallization to <8 kbar, between 350 and 450°C. The mineral assemblage representing the greenschist episode suggests the P–T conditions of the high-pressure part of the chlorite or lower biotite zone. The latest metamorphic recrystallization, under the greenschist facies, may have taken place in the Viséan.     

The origin of brown hornblende in the Artfjället gabbro and dolerites

Brown hornblende occurs in minor amounts in the Artfjället gabbro and dolerites, except in quartz-dolerites where a pale green hornblende occurs. In the gabbro, brown hornblende is mostly Ti-bearing pargasite or kaersutite. It occurs along veins of orthopyroxene, as rims around and blebs in pyroxenes, with orthopyroxene in coronas between olivine and plagioclase and in coronas between ilmenite and plagioclase. In the olivine-dolerites and orthopyroxene-dolerites brown hornblende is ferroan titanian pargasite or ferroan kaersutite. The pale green hornblende in the quartz-dolerites is a magnesio-hornblende. The hornblendes in the dolerites are interstitial or granular, in some dolerites occurring as coarse oikocrysts. It is proposed that under certain conditions the Ti content of hornblende can be used as a thermometer, derived from experimental data of Helz (1973). Microstructures, compositions and formation temperatures (< 1,040° C) show that the brown hornblende in the gabbro is not magmatic, but of subsolidus origin. Probably it formed as a result of the introduction of water into the gabbro during a deformation event that occurred early in the cooling history of the gabbro. Least-squares modelling of hornblende formation indicates that all magmatic minerals must have participated in the reaction and that the reaction probably was not isochemical. Microstructures, compositions and formation temperatures (1,030-965° C) of brown hornblende in the dolerites are consistent with late-stage crystallization from the magma. For the pale green hornblende in the quartz-dolerites a magmatic origin is likely, but cannot be proven.     

Alteration patterns and structural controls of the El Espino IOCG mining district,Chile

The El Espino IOCG mining district is characterized by several mineralized bodies the largest of which is the El Espino deposit, which has an estimated geologic resource of 123 Mt at 0.66 % Cu and 0.24 g/t Au. Mineralized bodies are distributed in a 7?×?10 km² area throughout a 1,000-m vertical section. They range from single veins to stockworks and breccias to manto-type deposits. The ore bodies are hosted primarily by volcanic, volcaniclastic, and sedimentary rocks of the Early Cretaceous Arqueros and Quebrada Marquesa formations, with a few mineralized zones within Late Cretaceous dioritic intrusions. The fault and vein architecture shows that El Espino IOCG system was localized within a dilatational jog along a major transtensional dextral fault system. Sodic alteration (albite) is the most extensive style of alteration in the district, and it is bounded by major NS–NNE trending faults. Sodic–calcic (epidote–albite) alteration occurs at deep to medium elevations (1,000–500 m) and grades inward into calcic alteration. Calcic alteration surrounds dioritic intrusions of the Llahuin plutonic suite. Significant iron oxides are associated with later calcic alteration associations (actinolite–epidote–hematite). The upper portions of the alteration system (0–500 m) display hydrolytic alteration associations with abundant hematite. Hydrolytic veins are feeders to zones of manto-type alteration and mineralization within favorable volcano-sedimentary lithologies that formed El Espino deposit. Sulfides are largely confined to calcic and hydrolytic alteration associations. Hydrothermal fluids responsible for hematite and sulfide mineralization had salinities between 32 and 34 wt% NaCl_eq and temperature of approximately 425 °C at an estimated depth of 3–4 km. Geochronological U–Pb and ⁴⁰Ar/³⁹Ar data indicate that hydrothermal alteration was coeval with magmatic intrusive activity. One particular dioritic intrusion (88.5 Ma) preceded the calcic stage (88.4 Ma), which was accompanied by iron oxide copper and gold mineralization. Hydrolytic alteration, related to economic iron oxide copper and gold mineralization, came immediately after at 87.9 Ma.     

Metamorphic differentiation at Einasleigh,Northern Queensland

Biotite‐muscovite‐garnet gneisses at Einasleigh contain quartz‐feldspar veins composed of the same minerals as found in the enclosing rock. The vein‐gneiss boundaries are commonly irregular and on a microscopic scale, gradational.

Certain amphibolite layers contain quartz‐feldspar veins composed of the same minerals as found in the amphibolite. Hornblende‐rich extraction zones surround these veins, and material balance calculations show that all or nearly all of the vein‐forming matter was locally derived. Variation in the abundance of hornblende and plagioclase in the amphibolite as a function of distance from a quartz‐feldspar vein can be expressed by error‐function curves, thus suggesting that the mineral‐segregation process was diffusion‐controlled. During the mineral rearrangement, the Na and Ca contents of plagioclase have evidently remained unchanged, but the vein hornblende has become slightly richer in Fe+3, Mg, and Ca, and poorer in Si and Al relative to hornblende in the adjacent amphibolite.

A certain biotite‐plagioclase rock forms layers and boudins in the gneisses and contains pegmatite veins composed of the same minerals as found in the host rock. The plagioclase in these veins is more sodic than that in the host rock while the biotite contains slightly more Ti and Fe+² and less Si and Mg than the biotite of the enclosing rock.

The data indicate that significant portions of the vein‐forming matter at Einasleigh were locally derived. The chemistry of some minerals has changed slightly during the segregation process, resulting possibly from different diffusion rates for the different mineral‐forming constituents.     

Orthopyroxene-bearing, mafic migmatites at Cone Peak, California: evidence for the formation of migmatitic granulites by anatexis in an open system

Abstract Orthopyroxene-bearing migmatites, exposed at the summit of Cone Peak in the Santa Lucia Range, California, offer an opportunity to explore potential links between granulite facies metamorphism and migmatite formation. Geothermobarometry indicates that the metamorphic temperatures and pressures were in the approximate ranges of 700–750° C and 7.0–7.5 kbar. The rocks at the summit comprise three domains: relatively coarse-grained, leucocratic veins; relatively fine-grained, biotite-enriched zones at the margins of the veins; and a biotite–hornblende-bearing host rock. Orthopyroxene is concentrated in the veins, which have also the highest ratio of anhydrous to hydrous minerals of the three rock types. The composition of the veins, together with their textures and modes, suggest that they formed through anatexis involving a dehydration-melting reaction which consumed hornblende and produced orthopyroxene. Variability in mineralogy and composition indicates that there was some local migration of magma along the veins before their final solidification. The biotite-enriched zones formed either by the concentration of residual biotite at the margins of the vein, or through the metasomatic conversion of hornblende (and/or pyroxene) to biotite, or by a combination of the two processes. Significant differences in the chemistry of the neosome (vein + biotite-enriched zone) and the host rock rule out simple dehydration melting in a local closed system. The model that explains best the mineralogical and chemical patterns involves triggering of melting by an influx of a low- a _H2O mixed fluid which added K and Si to and removed Ca from the neosome.     

A Report on a Biotite-Calcic Hornblende Geothermometer

This paper presents a biotite-calcic hornblende geothermometer which was empirically calibrated based on the gamet-biotite geothermometer and the gamet-plagioclase-hornblende-quartz geobarometer, in the ranges of 560-800℃ (T) and 0.26-1.4 GPa (P) using the data of metadolerite, amphibolite, metagabbro, and metapelite collected from the literature. Biotite was treated as symmetric Fe-Mg-AlVI-Ti quaternary solid solution, and calcic hornblende was simplified as symmetric Fe-Mg binary solid solution. The resulting thermometer may rebuild the input garnet-biotite temperatures well within an uncertainty of ±50℃. Errors of ±0.2 GPa for input pressure, along with analytical errors of ?% for the relevant mineral compositions, may lead to a random error of ±16℃ for this thermometer, so that the thermometer is almost independent of pressure estimates. The thermometer may clearly discriminate different rocks of lower amphibolite, upper amphibolite and granulite facies on a high confidence level. It is assume     

赛马-柏林川碱性杂岩常量组分变异的分离结晶制约

赛马－柏林川碱性杂岩体为侵位于古元古宙与新元古宙之间的缓倾斜岩席状岩体,缓倾的张裂隙制约了分异岩浆的侵位和含矿溶液的流通,交代富集的上地幔产生的富碱岩浆与富集的地壳产生的岩浆以不同比例混合,形成了正长质岩浆和霞石正长质岩浆。含地壳组分较高的正长质岩浆,受富钙辉石、角闪石和镁质较高黑云母的结晶分离制约向硅酸过饱和方向演化;霞石正长质岩浆受富钙辉石—霓辉石、白榴石、含Ｆｅ较高黑云母、黑榴石的分离结晶制约发生分异。稀土元素矿床是霞石正长质岩浆分异残余熔体的产物,侵位于岩体最高层位。     

Stable isotope evidence for magmatic fluid input during large-scale Na–Ca alteration in the Cloncurry Fe oxide Cu–Au district, NW Queensland, Australia

Sodic–calcic alteration is common in mineralized hydrothermal systems, yet the relative importance of igneous vs. basinal fluid sources remains controversial. One of the most extensive volumes of sodic–calcic rocks occurs near Cloncurry, NW Queensland, and was formed by overlapping hydrothermal systems that were active synchronously with emplacement of mid‐crustal batholithic granitoids (c. 1.55–1.50 Ga). Altered rocks contain albite–oligoclase, actinolite, diopside, titanite and magnetite. Alteration was localized by: (A) composite veins and breccias containing crystallized magma intimately intergrown with hydrothermal precipitates; (B) intrusions that host setting A veins and breccias; and (C) extensive breccia and vein systems linked to regional fault systems. Isotope analyses of actinolites in settings A and B indicate calculated δ¹⁸O_H2O (+8.2 to +10.6‰) and variably depleted δD_H2O (?130 to ?54‰) compared with typical magmatic fluids, whereas those from setting C typically indicate calculated δ¹⁸O_H2O (+8.0 to +12.8‰) and δD_H2O (?29 to ?99‰). The lowest δD_H2O values are interpreted as representing residual fluids after significant (> 90%) open‐system magmatic degassing. Overall the stable isotope, field, geochronological and geobarometric data suggest that these sodic–calcic alteration systems were formed by the episodic incursion of magmatic fluids that underwent minor isotopic modification as a result of varying degrees of interaction with country rocks.     

Platinum-group minerals from the Jinbaoshan Pd–Pt deposit,SW China: evidence for magmatic origin and hydrothermal alteration

The Jinbaoshan Pt–Pd deposit in Yunnan, SW China, is hosted in a wehrlite body, which is a member of the Permian (∼260 Ma) Emeishan Large Igneous Province (ELIP). The deposit is reported to contain one million tonnes of Pt–Pd ore grading 0.21% Ni and 0.16% Cu with 3.0 g/t (Pd + Pt). Platinum-group minerals (PGM) mostly are ∼10 μm in diameter, and are commonly Te-, Sn- and As-bearing, including moncheite (PtTe₂), atokite (Pd₃Sn), kotulskite (PdTe), sperrylite (PtAs₂), irarsite (IrAsS), cooperite (PtS), sudburyite (PdSb), and Pt–Fe alloy. Primary rock-forming minerals are olivine and clinopyroxene, with clinopyroxene forming anhedral poikilitic crystals surrounding olivine. Primary chromite occurs either as euhedral grains enclosed within olivine or as an interstitial phase to the olivine. However, the intrusion has undergone extensive hydrothermal alteration. Most olivine grains have been altered to serpentine, and interstitial clinopyroxene is often altered to actinolite/tremolite and locally biotite. Interstitial chromite grains are either partially or totally replaced by secondary magnetite. Base-metal sulfides (BMS), such as pentlandite and chalcopyrite, are usually interstitial to the altered olivine. PGM are located with the BMS and are therefore also interstitial to the serpentinized olivine grains, occurring within altered interstitial clinopyroxene and chromite, or along the edges of these minerals, which predominantly altered to actinolite/tremolite, serpentine and magnetite. Hydrothermal fluids were responsible for the release of the platinum-group elements (PGE) from the BMS to precipitate the PGM at low temperature during pervasive alteration. A sequence of alteration of the PGM has been recognized. Initially moncheite and atokite have been corroded and recrystallized during the formation of actinolite/tremolite, and then, cooperite and moncheite were altered to Pt–Fe alloy where they are in contact with serpentine. Sudburyite occurs in veins indicating late Pd mobility. However, textural evidence shows that the PGM are still in close proximity to the BMS. They occur in PGE-rich layers located at specific igneous horizons in the intrusion, suggesting that PGE were originally magmatic concentrations that, within a PGE-rich horizon, crystallized with BMS late in the olivine/clinopyroxene crystallization sequence and have not been significantly transported during serpentinization and alteration.     

Thermodynamics of multicomponent pyroxenes: II. Phase relations in the quadrilateral

The model for the thermodynamic properties of multicomponent pyroxenes (Part I) is calibrated for ortho- and clinopyroxenes in the quadrilateral subsystem defined by the end-member components Mg₂Si₂O₆, CaMgSi₂O₆, CaFeSi₂O₆, and Fe₂Si₂O₆. This calibration accounts for: (1) Fe-Mg partitioning relations between orthopyroxenes and augites, and between pigeonites and augites, (2) miscibility gap features along the constituent binary joins CaMgSi₂O₆-Mg₂Si₂O₆ and CaFeSi₂O₆-Fe₂Si₂O₆, (3) calorimetric data for CaMgSi₂O₆-Mg₂Si₂O₆ pyroxenes, and (4) the P-T-X systematics of both the reaction pigeonite=orthopyroxene+augite, and miscibility gap featurs, over the temperature and pressure ranges 800–1500°C and 0–30 kbar. The calibration is achieved with the simplifying assumption that all regular-solution-type parameters are constants independent of temperature. It is predicated on the assumptions that: (1) the Ca-Mg substitution is more nonideal in Pbca pyroxenes than in C2/c pyroxenes, and (2) entropies of about 3 and 6.5 J/K-mol are associated with the change of Ca from 6- to 8-fold coordination in the M2 site in magnesian and iron C2/c pyroxenes, respectively. The model predicts that Fe²⁺-Mg²⁺ M1-M2 site preferences in C2/c pyroxenes are highly dependent on Ca and Mg contents, with Fe²⁺ more strongly preferring M2 sites both in Ca-rich C2/c pyroxenes with a given Fe/(Fe+Mg) ratio, and in magnesian C2/c pyroxenes with intermediate Ca/(Ca+Fe+Mg) ratios.The proposed model is internally consistent with our previous analyses of the solution properties of spinels, rhombohedral oxides, and Fe-Mg olivines and orthpyroxenes. Results of our calibration extend an existing database to include estimates for the thermodynamic properties of the C2/c and Pbca pyroxene end-members clinoenstatite, clinoferrosilite, hedenbergite, orthodiopside, and orthohedenbergite. Phase relations within the quadrilateral and its constitutent subsystems are calculated for temperatures and pressures over the range 800–1700°C and 0–50 kbar and compare favorably with experimental constraints.     

Two different pyroxene crystallisation trends in the trough bands of the Skaergaard Intrusion,East Greenland

Pyroxenes and olivines from the trough bands in the Upper Zone (UZa) of Skaergaard Intrusion have been investigated, together with previously analysed pyroxenes (Brown, 1957; Brown and Vincent, 1963) and olivines from the Layered Series ferrodiorites. The electron microprobe, electron microscope, and analytical electron microscope EMMA-4 were used. Results show a striking difference between the cumulus and intercumulus trends of the trough-band pyroxenes. The cumulus trend follows that of the main Layered Series whereas the intercumulus trend shows a shrinking of the miscibility gap together with great enrichment in the Fs molecule, the miscibility gap being symmetrical about ～Wo₂₄. The shrinking appears to be a function of the different crystallisation conditions in the intercumulus liquid which was closed off in “cells” from the main mass of supernatant liquid. Enrichment in the Fs molecule is due to the much lower crystallisation temperatures of the intercumulus pyroxenes. Iron enrichment is also reflected in the intercumulus olivines. For the cumulus trend, Brown's calcium-poor pyroxene trend (1957) has been extended into more iron-rich parts of the pyroxene quadrilateral, well after olivine has reappeared and subsequent to the increase in calcium of the ferroaugites. The subsolidus trend for pyroxenes in the Fs-rich region has also been established.