Ultra-high-pressure (UHP) marble and eclogite in the Su-Lu UHP terrane, eastern China

A large mass of dolomitic marble including many eclogite blocks occurs in orthogneisses of the Rongcheng area of the Su-Lu province, eastern China. The marble consists mainly of dolomite, calcite (formerly aragonite), graphite, forsterite, diopside, talc, tremolite and phlogopite. Aggregates of talc and calcite occur at the boundary between dolomite and diopside. Tremolite is a reaction product between talc and calcite. Eclogite blocks are rimmed by dark green amphibolite. The primary mineral assemblage in the core of eclogite is Na-bearing garnet (up to 0.2  wt% Na₂O), omphacitic pyroxene, clintonite and rutile. Secondary minerals are pargasitic/edenitic amphibole, plagioclase, sodic diopside, chlorite, zoisite and titanite. The peak metamorphic conditions, based on stability of the dolomite+forsterite+aragonite (now calcite)+graphite assemblage, under conditions where tremolite is unstable, are estimated at T  =610–660 °C and P =2.5–3.5  GPa (for X _{CO=0.001). A reaction between dolomite and diopside to form talc under tremolite-unstable conditions indicates a temperature decrease under ultra-high-pressure conditions (} P >2.4  GPa, X _{CO<0.0013). The formation of secondary tremolite is consistent with a nearly adiabatic pressure decrease post-dating the ultra-high-pressure metamorphism. The temperature decrease under ultra-high-pressure conditions preceding decompression may reflect the underplating of a cold slab, and the rapid decompression probably corresponds to the upwelling stage promoted by the delamination of a downwelling lithospheric root. The} P – T  conditions of the amphibolitization stage are estimated at <0.9  GPa and <460 °C, and are similar to conditions recorded by the surrounding orthogneisses.     

P-T-X (CO2) conditions in mafic and calc-silicate hornfelses from Oberon, New South Wales, Australia

Abstract The Rockley Volcanics from near Oberon, New South Wales occur within the aureole of the Carboniferous Bathurst Batholith and have been contact metamorphosed at P ∼ 100 ± 50MPa (10.5kbar) and a maximum T ∼ 565°C in the presence of a C–O–H fluid. Prior to contact metamorphism the volcanics were regionally metamorphosed and altered with the extensive development of actinolite, chlorite, plagioclase, quartz and calcite. The contact metamorphosed equivalents of these rocks have been subdivided into: Ca-poor (cordierite + gedrite), Mg-rich (amphibole + olivine + spinel), mafic (amphibole + plagioclase) and Ca-rich (amphibole + garnet + diopside; diopside + plagioclase; garnet + diopside + wollastonite) rocks.
The chemistry of the minerals in the hornfelses was controlled by the bulk rock chemistry and fluid composition. Pargasites and hastingsites as well as an unusual phlogopite with blue green pleochroism, are found in Ca-rich hornfelses. A comparison of the assemblages with experimentally derived equilibria suggests that the fluid phase associated with the Ca-rich hornfelses was water-rich (X_co2= 0.1 to 0.3) while that associated with the Mg-rich hornfelses was enriched in CO₂ (X_co2 > 0.7). The different hornfels types have reacted to contact metamorphism independently in both their solid and fluid chemistries.     

湖南省柿竹园矽卡岩矿床中石榴石特征

通过野外与显微镜观察和电子探针分析, 对柿竹园多金属矿床矽卡岩中石榴石的特征进行了研究.根据石榴石的产出状态、矿物的共生组合, 矽卡岩可分为4个带: 磁铁矿-辉石-石榴石带、辉石-石榴石带、符山石-石榴石带、矽卡岩化大理岩带.从成分上的变化, 探讨了石榴石在各矽卡岩带中的特征.柿竹园矿床矽卡岩中的石榴石可分为早、晚两期, 早期形成的石榴石颜色为暗棕色, 并且在垂直和水平方向上有明显的变化规律.从磁铁矿-辉石-石榴石带到矽卡岩化大理石带, 随着石榴石中Fe₂O₃含量的减少, Al₂O₃含量的增加, 由钙铁榴石向钙铝榴石变化; 石榴石晶体具有从核部向边缘由均质性向非均质性变化的规律.早期石榴石形成于较氧化的条件下, 温度为520~620℃, 压力为1000×105Pa, 由富含Si, Al, Fe, Cl, F组分的热液和泥盆纪佘田桥组灰岩反应交代形成.当温度降至450~ 540℃, pH, Eh值降低时, 晚期石榴石形成的同时使白钨矿沉淀.晚期石榴石颜色比早期形成的石榴石浅, 为红色.结晶颗粒较大, 并且, 普遍可以观察到石榴石环带结构.      

Diffusion-controlled corona reaction and overstepping of equilibrium in a garnet granulite, Yenisey Ridge, Siberia

Diffusion modelling is applied to layered garnet–pyroxene–quartz coronas, formed by a pressure-induced reaction between plagioclase and primary pyroxene in a metabasic granulite. The reconstructed reaction involves some change in composition of reactant minerals. The distribution of minerals between layers is satisfactorily explained by diffusion-controlled reaction with local equilibrium, in which the diffusion coefficient for Al was smaller than those for Fe, Mg and Ca by a factor of approximately four. Diffusion of Mg towards plagioclase implies a chemical-potential gradient for MgO component in a direction opposite to the changing Mg content of garnet; this is explained by the influence of Al₂O₃ on the chemical potential of the pyrope end-member. Grain-boundary diffusion is suggested to have operated, possibly with composition gradients different from those in the bulk minerals. Chemical-potential differences across the corona are estimated from the variation in garnet composition, enabling affinity (the free energy change driving the reaction) to be estimated as 6.9±1.8  kJ per 24-oxygen mole of garnet produced. This implies that the pressure for equilibrium among the minerals was overstepped by 1.4±0.4  kbar. The probable P–T conditions of reaction were in the range 650–790  °C, 8–10  kbar. Assuming a timescale of reaction between 10⁶ and 10⁸ years, estimated diffusion coefficients for Fe, Mg and Ca are in the range 9×10⁻²³ to 5×10⁻²⁰ m² s⁻¹. These are consistent with experimental values in the literature for solid-state diffusion, including grain-boundary diffusion.     

Impure marbles from the UHP Brossasco-Isasca Unit (Dora-Maira Massif, western Alps): evidence for Alpine equilibration in the diamond stability field and evaluation of the X(CO2) fluid evolution

Two impure ultrahigh-pressure (UHP) marbles, a calcite marble with the peak assemblage Grt + Phe + Cpx + Rt + (Arg) and a dolomite marble with the peak assemblage Crn + Chl + Rt + Dol (±Arg), from the same lens from the polymetamorphic complex of the Brossasco-Isasca Unit (BIU) (southern Dora-Maira Massif) have been petrologically investigated and modelled by calculating P – T phase-diagram projections for H₂O–CO₂ mixed-volatile systems. Thermobarometric data obtained from the calcite marble suggest Alpine peak conditions in the diamond stability field (4.0 GPa at 730 °C), and allow reconstruction of the earlier portion of the Alpine retrograde P – T path, which is characterized by a significant decompression coupled with a moderate and continuous cooling to 650 °C at 2.50 GPa. The modelled fluid compositions at peak conditions point to 0.025 ≤  X (CO₂) ≤ 0.10 and X (CO₂) ≤ 0.0012 in the calcite marble and dolomite marble, respectively, suggesting fluid heterogeneity at the local scale and an internally buffered fluid evolution of the studied impure marbles. The lack of micro-diamond in the BIU marbles is explained by the very-low X (CO₂) values, which favoured relatively high f O₂-conditions, preventing the formation of diamond at the UHP peak metamorphic conditions.     

Contrasting mineral parageneses in high-temperature calc-silicate granulites: examples from the Eastern Ghats, India

Abstract Three types of mineral associations are described from calc-silicate granulites from the Eastern Ghats, India, where geothermobarometry in associated rocks suggests extremely high P–T conditions of metamorphism ( c . 9 ± 1 kbar, 950° C). These mineral associations are: (i) calcite + quartz + scapolite + plagioclase, (ii) calcite + scapolite + wollastonite + porphyroblastic garnet + coronal garnet and (iii) calcite + quartz + wollastonite + scapolite + porphyroblastic garnet + coronal garnet, all coexisting with K-feldspar, titanite and clinopyroxene. The first two associations evolved through nearly isobaric cooling retrograde paths, whereas the third evolved through a nearly isothermal decompression path followed by an isobaric cooling retrograde path. Textural and compositional characteristics suggest the following mineral reactions in the calc-silicate granulites: calcite + quartz = wollastonite + CO₂, calcite + plagioclase = scapolite, calcite + scapolite + wollastonite = porphyroblastic garnet ± quartz + CO₂, CaTs + wollastonite = coronal garnet (association ii) and wollastonite + scapolite = coronal garnet (association iii) + quartz + CO₂. Andradite content in garnet was buffered by the redox equilibria wollastonite + hedenbergite + O₂= andradite + quartz (association iii) and wollastonite + andradite + CaTs + scapolite = hedenbergite + calcite + grossular + O₂ (association ii). The contrasting mineral parageneses have been ascribed to interplay of variables such as X _CO2, f _O2, f _HCl in the fluid, bulk Na content and the nature of the retrograde P–T–X _CO2 paths through which the rocks evolved.     

A ternary solid solution model for omphacite and its application to geothermobarometry of eclogites from the Middle Adula nappe (Central Alps, Switzerland)

A ternary solid solution model for omphacite with the end-members jadeite (NaAlSi₂O₆), diopside (CaMgSi₂O₆) and hedenbergite (CaFeSi₂O₆) was derived from experimental data from the literature. The subregular solution model, fitted by linear programming, is best suited to omphacites with very little aegirine component in common eclogites. Applying this solution model to the calculation of equilibrium phase diagrams of eclogites from the Adula nappe (Central Alps, Switzerland) results in large stability fields for common eclogite assemblages (garnet+omphacite+quartz+H₂O±kyanite). Within this field the compositions of garnet and omphacite show very little variation. A precise determination of the peak-pressure and temperature is not possible. The occurrence of amphibole, overgrowing the peak-pressure assemblage in fresh eclogite, suggests retrograde re-equilibration, still under eclogite facies conditions. The computation of isopleths for garnet and pyroxene end-members allows the estimation of the pressure and temperature conditions of this re-equilibration event (19–21  kbar, c .  700 °C).     

Wollastonite and scapolite in Precambrian calc-silicate granulites from Australia and Antarctica

Abstract Scapolite, wollastonite, calcite, diopside, grossular-andradite garnet and sphene occur in calc-silicate rocks in the granulite terrain of the Arunta Block, central Australia. This assemblage buffers the CO₂ activity at a low value, so that any coexisting fluid phase must be H₂O rich and CO₂ poor ( X _co2 = 0.2-0.3). In contrast, the H₂O activity in the surrounding felsic and mafic granulites was low. Thus fluid activities during granulite facies metamorphism were locally buffered in various rock units and fluid flow appears to have been restricted or fluid may have been absent. Late retrograde rims of garnet and garnet-quartz separate phases formed in the high-grade stage. Formation of these rims would have required either an influx of water-rich fluid or a decrease in pressure. Evidence from the surrounding granulites shows that in one locality, the calc-silicate rocks had undergone late isobaric hydration; in another locality, minor uplift had occurred soon after peak P-T conditions. In both, scapolite had partly broken down to plagioclase-calite. A calc silicate rock from the granulite terrain of Enderby Land, Antarctica, contains scapolite, wollastonite, calcite, diopside, quartz and sphene; this assemblage also indicates low CO₂ activities. In this rock, wollastonite has broken down to calcite-quartz, to indicate isobaric cooling without influx of hydrous fluid.     

Calcite–graphite isotope thermometry in amphibolite facies marble, Bancroft, Ontario

This study presents calcite–graphite carbon isotope fractionations for 32 samples from marble in the northern Elzevir terrane of the Central Metasedimentary Belt, Grenville Province, southern Ontario, Canada. These results are compared with temperatures calculated by calcite–dolomite thermometry (15 samples), garnet–biotite thermometry (four samples) and garnet–hornblende thermometry (three samples). Δ_cal‐gr values vary regularly across the area from >6.5‰ in the south to 4.0‰ in the north, which corresponds to temperatures of 525 °C in the south to 650 °C in the north. Previous empirical calibration of the calcite–graphite thermometer agrees very well with calcite–dolomite, garnet–biotite and garnet–hornblende thermometry, whereas, theoretical calibrations compare less well with the independent thermometry. Isograds in marble based on the reactions rutile + calcite + quartz =titanite and tremolite + calcite + quartz = diopside, span temperatures of 525–600 °C and are consistent with calculated temperature–X(CO₂) relations. Results of this study compare favourably with large‐scale regional isotherms, however, local variation is greater than that revealed by large‐scale sampling strategies. It remains unclear whether the temperature–Δ_cal‐gr relationship observed in natural materials below 650 °C represents equilibrium fractionations or not, but the regularity and consistency apparent in this study demonstrate its utility for thermometry in amphibolite facies marble.     

Petrological characterization and tectonic significance of retrogressed garnet peridotites, Raobazhai area, North Dabie Complex, east-central China

The Raobazhai ultramafic body of the North Dabie Complex is re-interpreted as a mantle-derived peridotitic slice enclosed in, and isofacially metamorphosed with, surrounding granulite-to-amphibolite facies gneisses. The ultramafic sheet consists mainly of metaharzburgite, but includes subunits of metadunite and mylonitic lherzolite. The rocks contain spinel but neither garnet nor plagioclase. However, in the mylonitic lherzolite, fine-grained intergrowths of spinel, orthopyroxene and clinopyroxene outline domains resembling the habit of garnet in two dimensions; broad-beam microprobe analyses imply pseudomorphs after a pyropic garnet precursor. The mineral assemblage of the metadunite and metaharzburgite is: olivine (Fo₉₂)+orthopyroxene (En₉₂)+tremolitic-to-magnesiohornblende+Mg–Al-chromite, indicating amphibolite facies recrystallization. The mineral assemblage of the mylonitic lherzolite is: olivine (Fo₉₀)+orthopyroxene (En₉₀)+clinopyroxene+Cr-bearing spinel+pargasitic amphibole, indicative of granulite-to-amphibolite facies metamorphism. Phase equilibria and geothermometric estimations show that the Raobazhai meta-ultramafics have undergone at least three stages of recrystallization: (I) 950–990 °C, (II) 750–860 °C, and (III) 670–720 °C, assuming equilibrium in the spinel peridotite stability field ( c. 6–15 kbar), although an early, high-pressure stage (≥18 kbar) is probable, based on the inferred garnet pseudomorphs. Petrochemical and geothermobarometric data suggest that the ultramafic slice represents a fragment of the mantle wedge, tectonically incorporated into subducted continental crust and re-equilibrated at granulite-to-amphibolite facies conditions while being exhumed to shallow levels.     

Geochemical self-organization of olivine-grade contact metamorphosed chert nodules in dolomite marble, Kilchrist, Skye

Chert nodules in dolostones in the aureole of the Tertiary Beinn an Dubhaich granite, Skye, have developed  mm-scale concentric monomineralic bands of alternating calcite and olivine during breakdown of a diopside core by the reaction 3 Dol+Di=4 Cal+2Fo+2 CO₂. A simple textural progression from thin (<1 cm) homogeneous olivine-calcite rims close to the olivine-in isograd, to total replacement of the diopside core by a ≤10 cm thick well-banded rim close to the carbonate-granite contact demonstrates the developmental stages of the patterning. Correlation of olivine grain size with band spacing, and a greater olivine grain size in banded compared with homogeneous rims support pattern development by post-nucleation geochemical self-organization.     

Reaction textures in calc-silicate granulites from the Bolingen Islands, Prydz Bay, East Antarctica: implications for the retrograde P–T path

Calc-silicate granulites from the Bolingen Islands, Prydz Bay, East Antarctica, exhibit a sequence of reaction textures that have been used to elucidate their retrograde P–T path. The highest temperature recorded in the calc-silicates is represented by the wollastonite- and scapolite-bearing assemblages which yield at least 760°C at 6 kbar based on experimental results. The calc-silicates have partially re-equilibrated at lower temperatures (down to 450°C) as evidenced by the successive reactions: (1) wollastonite + scapolite + calcite = garnet + CO₂, (2) wollastonite + CO₂= calcite + quartz, (3) wollastonite + plagioclase = garnet + quartz, (4) scapolite = plagioclase + calcite + quartz, (5) garnet + CO₂+ H₂O = epidote + calcite + quartz, and (6) clinopyroxene + CO₂+ H₂O = tremolite + calcite + quartz.
The reaction sequence observed indicates that a CO₂ was relatively low in the wollastonite-bearing rocks during peak metamorphic conditions, and may have been further lowered by local infiltration of H₂O from the surrounding migmatitic gneisses on cooling. Fluid activities in the Bolingen calc-silicates were probably locally variable during the granulite facies metamorphism, and large-scale CO₂ advection did not occur.
A retrograde P–T path, from the sillimanite stability field ( c. 760°C at 6 kbar) into the andalusite stability field ( c. 450°C at <3 kbar), is suggested by the occurrence of secondary andalusite in an adjacent cordierite–sillimanite gneiss in which sillimanite occurs as inclusions in cordierite.     

Anti-clockwise P–T paths in the lower crust: an example from a kyanite-bearing regional aureole, George Sound, New Zealand

The George Sound Paragneiss (GSP) represents a rare Permo-Triassic unit in Fiordland that occurs as a km-scale pillar to gabbroic and dioritic gneiss of c . 120 Ma Western Fiordland Orthogneiss (WFO). It is distinguished from Palaeozoic paragneiss common in western Fiordland (Deep Cove Gneiss) by SHRIMP and laser-ablation U–Pb ages as young as c . 190 Ma and ¹⁷⁶Hf/¹⁷⁷Lu >0.2828 for detrital zircon grains. The Mesozoic age of the GSP circumvents common ambiguity in the interpretation of Cretaceous v. Palaeozoic metamorphic assemblages in the Deep Cove Gneiss. A shallowly dipping S₁ foliation is preserved in the GSP distal to the WFO, cut by 100 m scale migmatite contact zones. All units preserve a steeply dipping S₂ foliation. S₁ staurolite and sillimanite inclusions in the cores of metapelitic garnet grains distal to the WFO preserve evidence for prograde conditions of T  <   650 °C and P <  8 kbar. Contact aureole and S₂ assemblages include Mg-rich, Ca-poor cores to garnet grains in metapelitic schist that reflect WFO emplacement at ≈760 °C and ≈6.5 kbar. S₂ kyanite-bearing matrix assemblages and Ca-enriched garnet rims reflect ≈650 °C and ≈11 kbar. Poorly oriented muscovite–biotite intergrowths and rare paragonite reflect post-S₂ high- P retrogression and cooling. Pseudosection modelling in NCKFMASH defines a high- P anti-clockwise P–T history for the GSP involving: (i) mid- P amphibolite facies conditions; preceding (ii) thermal metamorphism adjacent to the WFO; followed by (iii) burial to high- P and (iv) high- P cooling induced by tectonic juxtaposition of cooler country rock.     

Active skarn formation beneath Lascar Volcano, northern Chile: a petrographic and geochemical study of xenoliths in eruption products

Calcsilicate xenoliths occur in large numbers in some lavas and pyroclastic flows of Lascar Volcano. Their whole-rock major element and REE compositions indicate that the protolith was the Upper Cretaceous Yacoraite Formation, which crops out extensively in NW Argentina. The whole-rock major element compositions of the xenoliths fall into specific groups suggesting a strong geochemical zonation in the skarn zone. Three geochemical zones have been identified; (1) an outer metamorphic zone rich in wollastonite; (2) a middle zone rich in pyroxene and garnet; (3) an inner zone rich in pyroxene and magnetite. The two innermost zones have developed from the wollastonite zone by infiltration of metasomatic fluids rich in Fe, Mn, Mg, Ti and Al. Whole-rock REE patterns have not changed significantly during prograde metamorphism and metasomatism, indicating REE immobility in the altering fluids. Retrograde alteration by acid-sulphate fluids produced anhydrite skarns and secondary calcite and wilkeite veins in the wollastonite zone. The carbon and oxygen isotopic compositions of this calcite indicate that it formed by Rayleigh crystallization from a low-temperature (<200 °C) fluid containing dissolved H₂CO₃. The calculated δ¹⁸O of the water in this fluid suggests a magmatic origin whereas the calculated δ¹³C of the dissolved carbonate is consistent with derivation from rocks of the Yacoraite Formation at 350 °C. It is suggested that the magmatic acid-sulphate fluid was responsible for leaching carbonate from the surrounding carbonate rocks and redepositing it in the skarn zone. REEs were mobilized during the retrograde acid-sulphate and acid-carbonate alteration. A negative Ce anomaly associated with this carbonate and sulphate indicates high oxygen fugacities in the mineralizing fluids.     

Metamorphic phase relations in orthopyroxene-bearing granitoids: implication for high-pressure metamorphism and prograde melting in the continental crust

In this work, the factors controlling the formation and preservation of high-pressure mineral assemblages in the metamorphosed orthopyroxene-bearing metagranitoids of the Sandmata Complex, Aravalli-Delhi Mobile Belt (ADMB), northwestern India have been modelled. The rocks range in composition from farsundite through quartz mangerite to opdalite, and with varying K₂O, Ca/(Ca + Na)_rock and FeO_tot + MgO contents. A two stage metamorphic evolution has been recorded in these rocks.
An early hydration event stabilized biotite with or without epidote at the expense of magmatic orthopyroxene and plagioclase. Subsequent high-pressure granulite facies metamorphism (∼15 kbar, ∼800 °C) of these hydrated rocks produced two rock types with contrasting mineralogy and textures. In the non-migmatitic metagranitoids, spectacular garnet ± K-feldspar ± quartz corona was formed around reacting biotite, plagioclase, quartz and/or pyroxene. In contrast, biotite ± epidote melting produced migmatites, containing porphyroblastic garnet incongruent solids and leucosomes.
Applying NCKFMASHTO T–M (H₂O) and P–T pseudosection modelling techniques, it is demonstrated that the differential response of these magmatic rocks to high-pressure metamorphism is primarily controlled by the scale of initial hydration. Rocks, which were pervasively hydrated, produced garnetiferous migmatites, while for limited hydration, the same metamorphism formed sub-solidus garnet-bearing coronae. Based on the sequence of mineral assemblage evolution and the mineral compositional zoning features in the two metagranitoids, a clockwise metamorphic P–T path is constrained for the high-pressure metamorphic event. The finding has major implications in formulating geodynamic model of crustal amalgamation in the ADMB.     

滇西福贡亚五夺透闪玉矿物学特征及成因

在滇西福贡亚五夺地区普遍发育有规模不等的透闪石玉矿(化)体,呈不规则大脉状产于片麻岩、片岩的大理岩夹层与糜棱岩化花岗岩的接触部位。本文在系统调查矿床(体)地质的基础上,采用化学分析、粉晶X衍射及能谱分析等方法,研究了区内透辉石玉的宝石学、矿物学特征,进而对其成因进行探讨。透闪石玉矿石折射率1.60,硬度5.6,密度2.9g/cm~3±,达到玉石品质的指标要求,可作为一种新类型的软玉矿床开发;其主要矿物组成(体积分数)为透闪石(45%)、透辉石(40%),并含方解石(5%)、石英(5%),以及少量的长石、石榴石、磷灰石、榍石、独居石等;透闪石的SiO_2、CaO、MgO含量(质量分数)分别54.54%、22.32%、18.62%,并有少量的Fe_2O_3、Na_2O、Al_2O_3,其晶胞参数a0、b0、c0及β分别为0.978×10~(-10) m、1.785×10~(-10) m、5.284×10~(-10) m及104.45°。结合矿床地质特征以及矿石与围岩稀土元素示踪分析,该透闪石玉矿床仍属变质热液型矿床,但其是在区域性同岩浆同变形时期的拉张阶段,变质流体混合岩浆残余热液沿裂隙充填而成的,应是一种新的矿床成因类型。其成矿时期与碧罗雪山—崇山变形带喜马拉雅中晚期大规模的走滑剪切作用相关大体时限为22~15Ma。本区域具有同等地质背景和成矿条件的地段范围巨大,具有很大的找矿前景。     

Ultra-high-pressure metamorphism of carbonate rocks in the Dabie Mountains, central China

Abstract Widespread ultra-high-P assemblages including coesite, quartz pseudomorphs after coesite, aragonite, and calcite pseudomorphs after aragonite in marble, gneiss and phengite schist are present in the Dabie Mountains eclogite terrane. These assemblages indicate that the ultra-high-P metamorphic event occurred on a regional scale during Triassic collision between the Sino-Korean and Yangtze cratons. Marble in the Dabie Mountains is interlayered with coesite-bearing eclogite and gneiss and as blocks of various size within gneiss. Discontinuous boudins of eclogite occur within marble layers. Marble contains an ultra-high-P assemblage of calcite/aragonite, dolomite, clinopyroxene, garnet, phengite, epidote, rutile and quartz/coesite. Coesite, quartz pseudomorphs after coesite, aragonite and calcite pseudomorphs after aragonite occur as fine-grained inclusions in garnet and omphacite. Phengites contain about 3.6 Si atoms per formula unit (based on 11 oxygens). Similar to the coesite-bearing eclogite, marble exhibits retrograde recrystallization under amphibolite–greenschist facies conditions generated during uplift of the ultra-high-P metamorphic terrane. Retrograde minerals are fine grained and replace coarse-grained peak metamorphic phases. The most typical replacements are: symplectic pargasitic hornblende + epidote after garnet, diopside + plagioclase (An₁₈) after omphacite, and fibrous phlogopite after phengite. Ferroan pargasite + plagioclase, and actinolite formed along grain boundaries between garnet and calcite, and calcite and quartz, respectively. The estimated peak P–T conditions for marble are comparable to those for eclogite: garnet–clinopyroxene geothermometry yields temperatures of 630–760°C; the garnet–phengite thermometer gives somewhat lower temperatures. The minimum pressure of peak metamorphism is 27 kbar based on the occurrence of coesite. Such estimates of ultra-high-P conditions are consistent with the coexistence of grossular-rich garnet + rutile, and the high jadeite content of omphacite in marble. The fluid for the peak metamorphism was calculated to have a very low X_CO2 (<0.03). The P–T conditions for retrograde metamorphism were estimated to be 475–550°C at <7 kbar.     

Geochemistry of the Uintjiesberg kimberlite, South Africa: petrogenesis of an off-craton, group I, kimberlite

The Uintjiesberg kimberlite diatreme occurs within the Proterozoic Namaqua–Natal Belt, South Africa, approximately 60 km to the southwest of the Kaapvaal craton boundary. It is a group I, calcite kimberlite that has an emplacement age of 100 Ma. Major and trace element data, in combination with petrography, are used to evaluate its petrogenesis and the nature of its source region. Macrocryst phases are predominantly olivine with lesser phlogopite, with very rare garnet and Cr-rich clinopyroxene. Geochemical variation amongst the macrocrystic samples (Mg# 0.85–0.87, SiO₂=27.0–29.3%, MgO=26.1–30.5%, CaO=10.9–13.5%) is shown to result from 10% to 40% entrainment and partial assimilation of peridotite xenoliths, whereas that shown by the aphanitic samples (Mg# 0.80–0.83, SiO₂=19.1–23.0%, MgO=17.9–23.9%, CaO=16.5–23.7%) is consistent with 7–25% crystal fractionation of olivine and minor phlogopite. Changing trajectories on chemical variation diagrams allow postulation of a primary magma composition with 25% SiO₂, 26% MgO, 2.3% Al₂O₃, 5%H₂O, 8.6% CO₂ and Mg#=0.85.

Forward melting models, assuming 0.5% melting, indicate derivation of the primary Uintjiesberg kimberlite magma from a source enriched in light rare earth elements (LREE) by 10× chondrite and heavy REE (HREE) by 0.8–2× chondrite, the latter being dependent on the proportion of residual garnet. Significant negative Rb, K, Sr, Hf and Ti anomalies present in the inferred primary magma composition are superimposed on otherwise generally smooth primitive mantle-normalized trace element patterns, and are inferred to be a characteristic of the primary magma composition. The further requirement for a source with chondritic or lower HREE abundances, residual olivine with high Fo content (Fo₉₄) suggests derivation from a mantle previously depleted in mafic melt but subsequently enriched in highly incompatible elements prior to kimberlite genesis. These requirements are interpreted in the context of melting of continental lithospheric mantle previously enriched by metasomatic fluids derived from a sublithospheric (plume?) source.     

A new occurrence of garnetiferous skarn rocks in Saudi Arabia: a case study from Bahrah area, Jeddah–Makkah Al Mukaramah highway

Metacarbonate rocks (including marble and skarn deposits) at Bahrah area are confined to a Precambrian island-arc suite made up mostly of massive basalts and volcaniclastics aligned in a NE-trending belt. The marbles are either pure (almost made up of calcite) or contain considerable amounts of tremolite, actinolite, epidote, and diopside. Garnet-bearing rocks at Bahrah area are classified into garnetiferous marble and skarn calc-silicate assemblages that are described here for the first time. The calc-silicates become more abundant when the marble becomes interbedded with foliated metabasalt. Such contact is delineated by an epidote zone of variable thickness. Microscopically, the skarns are enriched in Ca-bearing minerals such as grossular garnet, epidote, titanite, diopside, and augitic salite. There are evidence that calc-silicate skarns were formed due to a thermal effect of a concealed underground shallow granitic intrusion. The basaltic rocks furnished Mg²⁺, Fe²⁺, Ti⁴⁺, and Al³⁺ that were first concentrated in the epidote zone. This was followed by pervasive replacement of epidote by large idiomorphic garnet (grossularite) that attains up to ～1.5 cm wide. It is evident that diopside is earlier than garnet with no replacement fabrics between the two minerals. Two types of titanite (sphene) can be distinguished: The first is secondary in the metabasalt host where titanite develops after titanomagnetite during regional metamorphism (i.e., metamorphic). On the other hand, the second type of titanite is found in the garnet-bearing calc-silicate skarn where it is typically euhedral with no link to any opaque phase and it is believed to be formed due to the event of superimposed thermal metamorphism (i.e., metasomatic). There are several evidence of the thermal metamorphic effect such as distinct granoblastic and annealing textures and K-metasomatism and formation of phlogopite at the expense of tremolite in the marble, in addition to poikiloblastic hornblende in the metabasalt host with distinct recrystallization. Also, there are some evidence of shearing such as brecciation along microshear planes, microfolding, introduction of fine euhedral pyrite, and presence of injected silica postdating crystallization of garnet in the calc-silicates.     

内蒙古大青山地区孔兹岩系中大理岩岩组的地球化学特征及原岩建造

大理岩岩组是内蒙古大青山地区孔兹岩系3个岩组中最上部的一个岩组,该岩组是一套富镁质的大理岩系,以巨厚的、大面积分布的白云质大理岩的发育为特征,底部有少量碎屑岩沉积,矿物组成除白云石外,普遍含蛇纹石化橄榄石、透辉石、金云母等一种或多种富镁硅酸盐矿物。岩石地球化学以富CaO、MgO和LOI为特征,反映了碳酸盐岩的地球化学特征,CaO＋MgO含量达44.96%以上,且CaO/MgO比值较小（1.37～10.94）,其原岩应为一套碎屑含量极低的白云岩,以化学沉积为主。原岩建造的沉积环境：由初期的陆海过渡的三角洲相,过渡到滨海-浅海相,最后到干燥气候条件下有障蔽岛相隔的封闭海盆相。构造环境也从亚稳定状态过渡到稳定构造环境,表明该套变质沉积地层的原岩可能形成于被动大陆边缘,但更类似于中元古界长城系、蓟县系这样的克拉通内裂陷槽或裂谷沉积。