Mass transfer and porosity evolution during low temperature water–rock interaction in gneisses of the simano nappe: Arvigo,Val Calanca,Swiss Alps

Late Alpine fissures and fractures in amphibolite-facies basement gneisses at Arvigo (Val Calanca, Swiss Alps) show distinct cm-sized reaction selvages parallel to the fracture walls that composed of subgreenschist facies assemblages produced by the interaction of water present in the fracture porosity with the old high-grade gneiss assemblages. The process of selvage or reaction-vein formation occurred in the brittle deformation regime and at temperatures characteristic of, first the prehnite-pumpellyite facies and then later of the zeolite facies. The vein formation occurred during uplift and cooling at very late stages of the Alpine orogeny. The reaction veins are composed of a selvage of altered gneiss on both sides of the central fracture and a central zone with fissure minerals that have been growing in the open fracture pore space. The central zone of the Arvigo veins contains an early assemblage with epidote, prehnite and chlorite and a late succession sequence of various species of zeolite. The veins of the Arvigo quarry are convincing evidence that fracture fluids in gneiss and granite have the potential to precipitate Ca–zeolite. This is an important find because many fluids recovered from deep continental drill holes and from geothermal energy exploration are found to be oversaturated in respect to a number of Ca–zeolite species. Vein formation during late uplift and cooling of the Alps occurred at continuously decreasing T and at hydrostatic pressure: (1) coexisting prehnite/epidote records temperatures of 330–380°C, (2) chlorite formation at temperature of 333 ± 32°C and (3) formation of zeolites <250°C. In the selvages the prime reaction is the replacement of plagioclase by albite along a sharp reaction front that separates the selvage from unaltered gneiss. In addition to albitisation, chloritisation of biotite is the second important reaction in the alteration process. The reactions release components for the formation of Ca–Al silicates. The water–rock interaction is associated with a depletion of Al, Si, Ca, Fe and K in the altered wall rock. The overall reaction is associated with an increase in porosity of up to 14.2 ± 2.2% in the selvage zone (altered wall rock), caused by the volume decrease during albitisation and the removal of biotite. The propagation of the sharp reaction front through the gneiss matrix occurred via a dissolution-reprecipitation mechanism. Zeolite formation is tied to the plagioclase alteration reaction in the rock matrix, which releases components for zeolite formation to a CO₂-poor aqueous liquid.     

Stable isotope and fluid inclusion evidence for the origin of the Brandberg West area Sn–W vein deposits, NW Namibia

The Brandberg West region of NW Namibia is dominated by poly-deformed turbidites and carbonate rocks of the Neoproterozoic Damara Supergoup, which have been regionally metamorphosed to greenschist facies and thermally metamorphosed up to mid-amphibolite facies by Neoproterozoic granite plutons. The meta-sedimentary rocks host Damaran-age hydrothermal quartz vein-hosted Sn–W mineralization at Brandberg West and numerous nearby smaller deposits. Fluid inclusion microthermometric studies of the vein quartz suggests that the ore-forming fluids at the Brandberg West mine were CO₂-bearing aqueous fluids represented by the NaCl–CaCl₂–H₂O–CO₂ system with moderate salinity (mean=8.6 wt% NaCl_equivalent).Temperatures determined using oxygen isotope thermometry are 415–521°C (quartz–muscovite), 392–447°C (quartz–cassiterite), and 444–490°C (quartz–hematite). At Brandberg West, the oxygen isotope ratios of quartz veins and siliciclastic host rocks in the mineralized area are lower than those in the rocks and veins of the surrounding areas suggesting that pervasive fluid–rock interaction occurred during mineralization. The O- and H-isotope data of quartz–muscovite veins and fluid inclusions indicate that the ore fluids were dominantly of magmatic origin, implying that mineralization occurred above a shallow granite pluton. Simple mass balance calculations suggest water/rock ratios of 1.88 (closed system) and 1.01 (open system). The CO₂ component of the fluid inclusions had similar δ ¹³C to the carbonate rocks intercalated with the turbidites. It is most likely that mineralization at Brandberg West was caused by a combination of an impermeable marble barrier and interaction of the fluids with the marble. The minor deposits in the area have quartz veins with higher δ ¹⁸O values, which is consistent with these deposits being similar geological environments exposed at higher erosion levels.     

Geological Implications for the Deep-Derived Mafic Enclaves from Cenozoic Shoshonitic Rocks in Jianchuan-Dali Area,West Yunnan

1ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅＡｉｌａｏｓｈａｎ ＪｉｎｓｈａｊｉａｎｇＣｅｎｏｚｏｉｃａｌｋａｌｉ ｒｉｃｈｐｏｔａｓｓｉｃｍａｇｍａｔｉｃｂｅｌｔｅｘｔｅｎｄｓｏｖｅｒａｄｉｓｔａｎｃｅｏｆ370 0ｋｍｉｎｔｈｅＮＷ ＮＷＷｄｉｒｅｃｔｉｏｎ (ＺｈａｎｇＹｕｑｕａｎａｎｄＸｉｅＹｉｎｇｗｅｎ ,1 997) .Ｓｔｕｄｉｅｓｏｆｐｅｔｒｏｌｏｇｙａｎｄｇｅｏｃｈｅｍｉｓｔｒｙｉｎｄｉｃａｔｅｔｈａｔｔｈｅｉｎｔｅｒｍｅｄｉａｔｅｔｏｉｎｔｅｒｍｅｄｉａｔｅ ａｃｉｄａｌｋａｌｉ ｒｉｃｈｐｏｒｐｈｙｒｙｇｒ…     

Rock—Forming and Ore—Forming Temperatures of Lianhuashan Tungsten Deposit,Guangdong Province

The Lianhuashan tungsten deposit occurs in the volcanic terrain in the coastal area of Southeast China,where rhyolite,quartz porphyry and granite consitute a complee magmatic series.The orebodies are located in the endo-and exo-contacts between the quartz porphyry and the metasandstone of the Xiaoping coal measues.Hongenization temperatures of melt inclusions in zircon and quartz are 1100℃and 1050℃ for rhyolite,1000℃ and 860℃for quartz porphyry,and 950-1000℃and 820℃ for granite,respectively,demonstrating that the rockforming temperatures dropped successively from the eruptive to the intrusive rocks and that the homogenization temperatures of melt inclusions in zircon are 50-180℃higher than those in quartz.Homogenization temperatures of gas-liquid inclusions in quartz are 230-520℃（mostly 230-270℃）for quartz porphyry,200-450℃（mostly 200-360℃）for ore-bearing quartz veins,150-210℃for granite 170-200℃ for the vein quartz in it.Quartz from the quartz porphyry and from the ore-earing quartz veins show similar characteristics in inclusion type and homogenization temperature,indicating that intergranular solutions must have been formed upon cooling of magma and that ore-forming solutions for the tungstem mineralization were evolved mainly from ore-bearing intergranular solutions in the quartz porphyry.     

Petrology and thermobarometry of eclogite rocks in the Krasnaya Guba dike field,belomorian mobile belt

A sequence of mineral associations was examined in eclogitized basites of the Krasnaya Guba dike field in the Belomorian Mobile Belt. Two morphological types of eclogite and eclogite-like rocks were recognized: (1) eclogite rocks that developed after ferrogabbro dikes and completely replaced these dikes from contact to contact and (2) eclogite-like rocks that developed after gabbronorites in zones of ductile deformations and shearing. According to data mineral geothermobaromety, both rock types were formed within temperature and pressure ranges corresponding to high-pressure and high-temperature amphibolite facies at T = 700 ± 40°C and P = 10.0 ± 0.5 kbar. The peak metamorphic parameters of the host gneisses are analogous. The decompressional stage, which is unambiguously identified by reaction textures, occurred at 630–660°C and 7.9–8.2 kbar. As the temperature and, first of all, pressure decreased, the SiO₂ activity in the fluid systematically varied. The eclogitization of the basites took place locally in relation to fluid fluxes, which were restricted to zones of intense deformations, at variable SiO₂ activity. The rocks show evidence of two stages of post-eclogite amphibolization. Older amphibolization 1 was coeval with the late prograde metamorphic stage (T = 650°C, P = 10–11 kbar). Younger amphibolization 2 affected eclogitized basite dikes and unaltered gabbronorites (together with their host gneisses) over large areas. This process coincided with decompression (T = 580°C, P = 7–8 kbar) and was likely accompanied by the exhumation of deep zones of BMB to upper-middle crustal levels.     

Fluid transfer of gold,palladium, and rare earth elements and genesis of ore occurrences in the Subpolar Urals

To estimate the behavior of Au, Pd, REE, and Y in magmatic and postmagmatic processes, a series of experimental studies on the solubility of noble metals and REE in magma, magmatic fluid, and hydrothermal solutions has been performed in wide temperature and pressure ranges (300–400°C, 860–1350°C; 1–14 kbar). The coefficients of Au and Pd partitioning (D ^F/L) between fluid and tholeiitic melt have been determined. Depending on P, T, and the composition of the system, they vary from 1 to 11 for Au and 0.02 to 1 for Pd. The phase solubility technique was used to determine Au and Pd solubility in hydrothermal fluid. The effects of temperature, composition, and fluid acidity on Au and Pd solubility have been estimated. The high solubility of these metals in aqueous chloride solutions has been established for both Au (28–803 mg/kg at T = 300°C, 305–1123 mg/kg at T = 350°C, and 330–1400 mg/kg at T = 400°C) and Pd (40–126 mg/kg at T = 300°C, 62–152 mg/kg at T = 350°C, and 20–210 mg/kg at T = 400°C). The coefficients of REE and Y partitioning (D ^F/L) between fluid and tholeiitic or alkaline melts have been determined. They vary from 0.00n to 2 depending on P, T, and fluid composition. The experimental data on Au and Pd solubility in solutions and magmatic fluids and the wide variation of REE D ^F/L between fluid and melt show that magmatic and hydrothermal fluids are efficient agents of Au, Pd, and REE transfer and fractionation. The obtained experimental data were used for elucidating sources of fluids and their role in the genesis of Au-Pd-REE occurrences in the Subpolar Urals.     

The petrogenesis of basic and ultrabasic alkaline rocks of western Makhtesh Ramon,Israel: geochemistry,melt and fluid inclusion study

The basic and ultrabasic alkaline rocks of western Makhtesh Ramon, Israel crop out in numerous lava flows and subvolcanic bodies. The rock suite is composed of tephrite, basanite, basanitic nephelinite, analcimite, olivine nephelinite, and melilite-olivine nephelinite and in many outcrops is represented by glass-bearing varieties. Melt and fluid inclusions have been studied in olivine, clinopyroxene, and plagioclase phenocrysts. The EP, SIMS and microthermometry methods were used for inclusion study. The geochemical data obtained on glasses of melt inclusions (major, REE, trace elements, volatiles) are compared with the data on whole-rock and groundmass glass compositions. The compositions of melt inclusions reflect the different stages of rock crystallization: the initial products of crystallization are similar to whole-rock compositions whereas final portions of melts are usually enriched in SiO₂, Al₂O₃, and alkalis, and depleted in mafic components. The data on contemporaneous melt and CO₂ inclusions were used for the evaluation of the P–T conditions of rock generation. The following parameters were obtained: tephrite: P = 6.3–7.7 kbar and T = 1,150–1,250°C; basanite: P = 6.6–9.2 kbar and T = 1,150–1,250°C; olivine and analcime-olivine nephelinite: P = 5.6–8.2 kbar and T = 1,150–1,250°C; melilite-olivine nephelinite: 4.0–5.4 kbar and T mainly between 1,150 and 1,200°C. Magma genesis was restricted to P–T conditions of spinel- and plagioclase-lherzolite fields. These data suggest the shallowest depth of magma genesis occurred in Makhtesh Ramon compared to other occurrences of Early Cretaceous magmatism at the Middle East. Differences in the degree of batch partial melting of the same source rocks best explain the diversity of the igneous suite in western Makhtesh Ramon.     

Problems of pressure estimation in high temperature experiments using solid media apparatus with particular reference to piston-cylinder and anvil-with-hole apparatus (Part I)

The high albite (Ab)⇄jadeite (Jd)+quartz(Q) reaction (1) and the quartz(Q)⇄coesite (Cs) transformation (2) have been determined within the temperature range of 1000–1100°C and 1000–1400°C respectively under variable pressures using an anvil-with-hole apparatus. The equilibrium curves for the two reactions as a function ofP andT are as follows: P=−1·33+0·0296T (reaction 1);P=18·949+0·0111T(reaction 2). These two lines intersect at 31·1±0·5kb and 1096°C. The possibility of using an anvil-with-hole apparatus for conducting current investigations is discussed in this paper.     

Metamorphic evolution of eclogite facies rocks in Northern Hubei and Southern Henan, China

Eclogite fades rocks in this area are diverse in rock type. The field occurrence and rock-chemistry reflect theirin-situ origin. Based on their regional geology and field occurrence, two groups of eclogites are divided in terms of their peak temperature of metamorphism. Medium-temperature eclogites (MT), as Group B, occur in the Dabie Group. They were formed from epidote-amphibolite facies. The metamorphism of eclogite facies has two stages: the coesite eclogite facies stage (the peak condition:T = 600 -700°C,P = 2.7-3.0 GPa) and the glaucophane eclogite facies stage (the pressure decreases, may be lower than 2.5 GPa while the temperature has little change). Low temperature eclogites (LT), as Group C, occur in the Qijiaoshan Formation. They were formed from blue schist facies (the peak condition:T = 490–560°C,P< 1.5 GPa). The appearance of hydrous minerals in the eclogites indicates the important role of water in metamorphism. Medium-temperature eclogites are different from low-temperature ones in metamorphism. At last, the evolution of the high-pressure metamorphic belt is discussed as well. This research project was financially supported by the National Natural Science Foundation of China (No. 49372100).     

Tracing the high pressure stage in the polymetamorphic Texel Complex (Austroalpine basement unit, Eastern Alps): P–T–t–d constraints

Summary Integration of new mineral chemical, geochronological and structural data from the Texel Complex yielded information on (re)crystallization and deformation processes in metapelites, eclogites and tonalitic orthogneisses during eclogite facies metamorphism. Maximum P–T conditions reached 1.2 to 1.4 GPa and 540–620 °C in the Upper Cretaceous. In tonalitic orthogneisses and metapelites, substantial garnet growth took place prior to eclogite facies metamorphism and Sm–Nd data indicate the presence of pre-Cretaceous mineral relics. In contrast, complex garnet-growth and -resorption processes are inferred for eclogites, which produced characteristic atoll microstructures and occurred close to the pressure peak of a single, coherent high pressure event. Garnet Sm–Nd data indicate eclogite facies crystallization at 85 ± 5 Ma. While eclogites retained information on the maximum burial stage, matrix phases in metapelites and orthogneisses were intensely recrystallized during the amphibolite facies metamorphic decompression. All the meso- and macro-scale deformation structures formed during the high pressure event and subsequent exhumation. The major mylonitic foliation is represented by the high pressure phases but was refolded during amphibolite facies exhumation. A biotite-whole-rock Rb–Sr age of 70–80 Ma indicates that cooling below about 300 °C occurred in the Upper Cretaceous. Supplementary material to this paper is available in electronic form at Appendix available as electronic supplementary material     

Metamorphic reactions between fluid inclusions and mineral hosts. I. Progress of the reaction calcite+quartz=wollastonite+CO2 in natural wollastonite-hosted fluid inclusions

 At the Bufa del Diente contact-metamorphic aureole, brine infiltration through metachert layers embedded in limestones produced thick wollastonite rims, according to Cc+Qz=Wo+CO₂. Fluid inclusions trapped in recrystallized quartz hosts include: (1) high salinity four phase inclusions [Th(V-L)=460–573° C; Td(salts)=350–400° C; (Na+K)_Cleq=64–73 wt%; X _{CO 2}≤0.02]; (2) low density vapour-rich CO₂-bearing inclusions [Th(L-V)≈500±100° C; X _{CO 2}=0.22–0.44; X _NaCl≤0.01], corresponding to densities of 0.27± 0.05 gcm⁻³. Petrographical observations, phase compositions and densities show that the two fluids were simultaneously trapped in the solvus of the H₂O-CO₂-salts system at 500–600° C and 700±200 bars. The low density fluid was generated during brine infiltration at the solvus via the wollastonite producing reaction. Identical fluid types were also trapped as inclusion populations in wollastonite hosts 3 cm adjacent to quartz crystals. At room temperature, both fluid types additionally contain one quartz and one calcite crystal, generated by the back-reaction Wo+CO₂=Cc+Qz of the host with the CO₂-proportion of the fluid during retrogression. All of the CO₂ was removed from the fluid. On heating in the microstage, the reaction progress of the prograde reaction was estimated via volume loss of the calcites. In vapour-rich fluids, 50% progress is reached at 490–530° C; 80% at 520–560° C; and 100% at 540–590° C, the latter representing the trapping temperatures of the original fluid at the two fluid solvus. The progress is volume controlled. With knowledge of compositions and densities from unmodified inclusions in quartz and using the equation of state of Duan et al. (1995) for H₂O-CO₂-NaCl, along with f _{CO 2}-values extracted from it, the reaction progress curve was recalculated in the P-T-X-space. The calculated progress curve passes through the two fluid solvus up to 380° C/210 bars, continues in the one fluid field and meets the solvus again at trapping conditions. The P-T slope is steep, most of the reaction occurs above 450° C and there is high correspondence between calculated and measured reaction progress. We emphasize that with the exception of quartz, back-reactions between inclusion fluids and mineral hosts is a common process. For almost any prograde metamorphic mineral that was formed by a devolatilization reaction and that trapped the equilibrium fluid or any peak metamorphic fluid as an inclusion, a fluid-host back-reaction exists which must occur somewhere along the retrograde path. Such retrograde reactions may cause drastic changes in density and composition of the fluid. In most cases, however, evidence of the evolving mineral assemblages is not given for they might form submicroscopical layers at the inclusion walls. Received: 15 March 1995 / Accepted: 1 June 1995     

Subduction-related P–T path for eclogites and garnet glaucophanites from the Samaná Peninsula basement complex, northern Hispaniola

Eclogite and garnet glaucophanite lenses from the Punta Balandra unit of the Samaná basement complex (northern Hispaniola) preserve information of the early metamorphic and tectonic history of subduction in the Caribbean island-arc and its collision with the North America plate. For this reason, P–T paths were reconstructed from the interpretation of meso- and microfabrics, mineral assemblages and chemistry, with the aid of equilibrium phase diagrams calculated for specific bulk compositions in the CKNFMASH system and isopleths for selected solution end-members. The obtained results suggest that the subduction-related prograde path evolved from garnet-free and garnet-bearing lawsonite-blueschist facies, to phengite eclogite facies conditions at P=22–24 kbar and T=610–625°C, with a probable intermediate stage of low-P lawsonite eclogite facies. The subsequent retrograde P–T path entered the epidote-blueschist (garnet-free) facies and ended within the greenschist facies field, similar to the prograde evolution at low-P. Eclogites and garnet glaucophanites formed in a subduction zone in which oceanic lithosphere was subducted WSW/W beneath the Caribbean plate.     

Metabasites with eclogite facies relics from Variscides in Sardinia,Italy: a review

Metabasites with eclogite facies relics occur in northern Sardinia as massive to strongly foliated lenses or boudins embedded within low- to medium-grade rocks (Anglona) and migmatites (NE Sardinia). U–Pb zircon dating yielded 453 ± 14, 457 ± 2 and 460 ± 5 Ma as the protolith ages; 400 ± 10 and 403 ± 4 Ma have been interpreted as the ages of the HP event and 352 ± 3 and 327 ± 7 Ma as the ages of the main Variscan retrograde events. A pre-eclogite stage is documented by the occurrence of tschermakite, zoisite relics within garnet porphyroblasts (Punta de li Tulchi) and an edenite–andesine inclusion within a relict kyanite porphyroblast (Golfo Aranci). Four main metamorphic stages have been distinguished in the eclogite evolution: (1) eclogite stage, revealed by the occurrence of armoured omphacite relics within garnet porphyroblasts. The Golfo Aranci eclogites also include kyanite, Mg-rich garnet and pargasite; (2) granulite stage, producing orthopyroxene and clinopyroxene–plagioclase symplectites replacing omphacite. At Golfo Aranci, the symplectitic rims around relict kyanite consist of sapphirine, anorthite, corundum and spinel; (3) amphibolite stage, leading to the formation of amphibole–plagioclase kelyphites between garnet porphyroblasts and pyroxene–plagioclase symplectites and to the growth of cummingtonite on orthopyroxene. Tschermakite to Mg-hornblende, plagioclase, cummingtonite, ilmenite, titanite and biotite are coexisting phases; (4) greenschist to sub-greenschist stage, defined by the appearance of actinolite, chlorite, epidote ss, titanite, sericite and prehnite. The following P–T ranges have been estimated for the different stages. Eclogite stage 550–700°C; 1.3–1.7 GPa; granulite stage 650–900°C; 0.8–1.2 GPa, clustering in the range 1.0–1.2 GPa; amphibolite stage 550–740°C; 0.3–0.7 GPa; greenschist stage 300–400°C; 0.2–0.3 GPa. Comparable ranges characterise the other Variscan massifs in Europe; eclogite stage: T = 530–800°C; P from 0.7–1.1 to 1.7 ± 0.3 GPa; granulite stage T = 760–870°C and P from 1.1–1.4 to 7.2–9.9 GPa, clustering around 1.0–1.2 GPa. Whole-rock chemistry: Sardinian eclogites are N- to T-MORB; European ones N- to E-MORB or calc-alkaline.     

熊耳山沙坡岭钼矿辉钼矿Re-Os定年及东秦岭晚侏罗世钼矿化的识别

河南沙坡岭矿床位于华北克拉通南缘的熊耳地体,产在燕山期花岗岩与围岩太华超群的外接触带,为东秦岭最近发现的细脉浸染型钼矿床。矿体受断裂或围岩裂隙控制,呈细脉、网脉状产出,矿石类型包括细脉状、浸染状和块状。为确定沙坡岭钼矿床成矿时代,本文利用辉钼矿Re-Os同位素定年,研究表明:采集的6件辉钼矿样品Re-Os单样年龄为158.3±1.5~160.7±1.2 Ma,其加权平均值为160±1 Ma(2σ误差,MSWD=2.1),指示沙坡岭钼矿化发生于晚侏罗世,且早于花山岩基约30 Ma,指示与花岗岩基无关。另外,一件产于花山复式岩体的团块状辉钼矿样品Re-Os单样年龄为130.5±1.0 Ma,与赋矿的花山岩体成岩时代一致,同样与前人报道的辉钼矿年龄(125.4~129.4 Ma)基本一致,且不存在明显的单颗粒辉钼矿187Os迁移,表明部分钼矿化形成于早白垩世。因此,辉钼矿Re-Os同位素定年显示沙坡岭矿床存在晚侏罗世和早白垩世两期钼矿化。结合矿床地质特征、成矿构造演化,认为沙坡岭钼矿与熊耳地体的花山岩基、花岗斑岩以及相关热液矿床,均属于秦岭造山带陆陆碰撞过程中挤压向伸展转变体制的产物。     

Geochemical characteristics and origin of Yangchuling porphyry W-Mo deposit

The Yangchuling porphyry W-Mo deposit is a new-type tungsten deposit discovered recently in southern China. Being of certain economic significance, this type of deposits promises some new prospects for the availability of increasing tungsten resource. The ore-bearing rock mass, intermediate to acid in composition, is a composite rock body resulting from comagmatic, multiple-stage intrusion during Middle-Late Yenshanian Period. Spatially, the rock mass is controlled by the Guangji—Anqing—Nanjing deep fault. As a typical porphyry deposit, the ore-bearing rocks (granodiorite porphyry, mozonitic granite porphyry and camouflage breccia) belong to sub-volcanic facies characteristic of near-surface environment. The rocks have suffered strong hydrothermal alteration which is closely related to mineralization. The deposit is classified as meso-epithermal deposit and our study shows that W and Mo come from the granodiorite, granodiorite porphyry and mozonitic granodiorite porphyry, which are believed to be derived through remelting from some W-rick basement rocks contaminated with minor amounts of upper mantle materials.     

Characterization of non-equilibrium and equilibrium occurrences of paragonite/muscovite intergrowths in an eclogite from the Sesia–Lanzo Zone (Western Alps, Italy)

 Coexisting muscovite and paragonite have been observed in an eclogite from the Sesia–Lanzo Zone (Western Alps, Italy). The P-T conditions of this eclogite reached 570–650 °C and 19–21 kbar and the rocks show several stages of mineral growth during their retrograde path, ranging from the subsequent lower-P eclogite facies to the blueschist facies and then the greenschist facies. Muscovite and paragonite are very common in these rocks and show two texturally different occurrences indicating equilibrium and non-equilibrium states between them. In one mode of occurrence they coexist in equilibrium in the lower-P eclogite facies. In the same rock muscovite ± albite also replaced paragonite during a greenschist-facies overprint, as evidenced by unique across – (001) layer boundaries. The chemical compositions of the lower-P eclogite-facies micas plot astride the muscovite – paragonite solvus, whereas the compositions of the greenschist-facies micas lie outside the solvus and indicate disequilibrium. The TEM observations of the textural relations of the greenschist-facies micas imply structural coherency between paragonite and muscovite along the layers, but there is a sharp discontinuity in the composition of the octahedral and tetrahedral sheets across the phase boundary. We propose that muscovite formed through a dissolution and recrystallization process, since no gradual variations toward the muscovite – paragonite interfaces occur and no intermediate, homogeneous Na-K phase has been observed. Because a solid-state diffusion mechanism is highly unlikely at these low temperatures (300–500 °C), especially with respect to octahedral and tetrahedral sites, it is assumed that H₂O plays an important role in this process. The across-layer boundaries are inferred to be characteristic of such non-equilibrium replacement processes. The characterization of these intergrowths is crucial to avoiding erroneous assumptions regarding composition and therefore about the state of equilibrium between both micas, which in turn may lead to misinterpretations of thermometric results. Received: 3 February 1999 / Accepted: 19 October 1999     

Link between convection and meridional gradient of sea surface temperature in the Bay of Bengal

We use daily satellite estimates of sea surface temperature (SST) and rainfall during 1998–2005 to show that onset of convection over the central Bay of Bengal (88–92°E, 14–18°N) during the core summer monsoon (mid-May to September) is linked to the meridional gradient of SST in the bay. The SST gradient was computed between two boxes in the northern (88–92°E, 18–22°N) and southern (82–88°E, 4–8°N) bay; the latter is the area of the cold tongue in the bay linked to the Summer Monsoon Current. Convection over central bay followed the SST difference between the northern and southern bay (ΔT) exceeding 0.75°C in 28 cases. There was no instance of ΔT exceeding this threshold without a burst in convection. There were, however, five instances of convection occurring without this SST gradient. Long rainfall events (events lasting more than a week) were associated with an SST event (ΔT ≥ 0.75°C); rainfall events tended to be short when not associated with an SST event. The SST gradient was important for the onset of convection, but not for its persistence: convection often persisted for several days even after the SST gradient weakened. The lag between ΔT exceeding 0.75°C and the onset of convection was 0–18 days, but the lag histogram peaked at one week. In 75% of the 28 cases, convection occurred within a week of ΔT exceeding the threshold of 0.75°C. The northern bay SST, T _N , contributed more to ΔT, but it was a weaker criterion for convection than the SST gradient. A sensitivity analysis showed that the corresponding threshold for T _N was 29°C. We hypothesise that the excess heating (∼1°C above the threshold for deep convection) required in the northern bay to trigger convection is because this excess in SST is what is required to establish the critical SST gradient.     

Franciscan eclogite revisited: Reevaluation of the P–T evolution of tectonic blocks from Tiburon Peninsula, California, U.S.A.

Summary High-grade blocks in the Franciscan complex at Tiburon, California, record relatively low temperature eclogite-facies metamorphism and blueschist-facies overprinting. The eclogite-facies mineral assemblage contains prograde-zoned garnet + omphacite + epidote ± hornblende (katophoritic and barroisitic Ca–Na amphibole) ± glaucophane + phengite (∼3.5 Si p.f.u.) ± paragonite + rutile + quartz. The blueschist-facies mineral assemblage contains chlorite + titanite + glaucophane + epidote ± albite ± phengite (∼3.3 Si p.f.u.). Albite is not stable in the eclogite stage. New calculations based on garnet-omphacite-phengite thermobarometry and THERMOCALC average-P–T calculations yield peak eclogite-facies P–T conditions of P = 2.2–2.5 GPa and T = 550–620 °C; porphyroclastic omphacite with inclusions of garnet and paragonite yields an average-P–T of 1.8 ± 0.2 GPa at 490 ± 70 °C for the pre-peak stage. The inferred counterclockwise hairpin P–T trajectory suggests prograde eclogitization of a relatively “cold” subducting slab, and subsequent exhumation and blueschist-facies recrystallization by a decreasing geotherm. Although an epidote-garnet amphibolitic assemblage is ubiquitous in some blocks, P–T pseudosection analyses imply that the epidote-garnet amphibolitic assemblage is stable during prograde eclogite-facies metamorphism. Available geochronologic data combined with our new insight for the maximum pressure suggest an average exhumation rate of ∼5 km/Ma, as rapid as those of some ultrahigh pressure metamorphic terranes.     

Theoretical Modelling of Water—Rock δD—δ18O Isotopic Exchange System and Source of OreForming Fluid：A Case Study on Jinduicheng Superlarge—Scale Molybdenum Deposti,Central China

Based on the theoretical modelling of water-rock δD-δ¹⁸O isotopic exchange process, the evolution and sources of ore-forming fluid in four metallogenic epochs of the Jinduicheng superlarge-scale porphyry-type molybdenum deposit were investigated. It was revealed that in the pre-metallogenic and early-metallogenic epochs, the ore-forming fluid was a residual fluid derived from magmatic water-wall rock interaction at middle to high temperatures (T = 250–500°C) and lower W/R ratios (0.1> = W/R>0.001), while in the metallogenic and postmetallogenic epochs, the ore-forming fluid was a residual fluid derived from meteoric water-wall rock interaction at middle to lower temperatures (T = 150–310°C) and relatively high W/R ratios (0.5>W/R≥0.1). The meteoric water played an important role in molybdenum mineralization, and at the main metallogenic epoch the W/R ratio reached its maximum value. This project was financially supported by both the National Natural Science Foundation of China and the Key Research Project of the Ministry of Geology and Mineral Resources of China.     

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.