大别山北部超高压变质大理岩及其地质意义

岩石学研究表明 ,大别山北部镁铁 超镁铁质岩带中白云质大理岩至少经历过三期变质阶段 :(1)榴辉岩相峰期变质阶段 ,矿物组合主要为方解石 +白云石 +金红石 +镁橄榄石 +钛 斜硅镁石 +富镁的钛铁矿±文石±石榴子石 ;(2 )麻粒岩相退变质阶段 ,矿物组合主要为方解石 +白云石 +金云母 +镁橄榄石 +透辉石 +钛铁矿 +尖晶石±斜方辉石等 ;(3)角闪岩相退变质阶段 ,主要矿物组合为方解石 +白云石 +磷灰石 +磁铁矿+榍石等。它的峰期变质矿物组合 ,类似于苏 鲁超高压大理岩 ,形成压力至少大于 2 .5GPa。这进一步证明 ,大别山北部大多数高级变质岩 (包括大理岩等 )都曾经过超高压变质作用 ,应属于印支期扬子俯冲陆壳的一部分。     

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.     

Well-preserved garnet growth zoning in granulite from the Dabie Mountains, central China

Ultra-high pressure eclogites and granulites both occur in the Dabie Mountains, central China. A garnet porphyroblast from felsic granulite in the Dabie Mountains has been analysed for compositional zoning by electron microprobe. Two segments of the porphyroblast have opposite compositional variations. Segment I (from centre outward 9  mm to analytical point 18) has decreasing X_Sps and increasing X_Pyr, while Segment II (from analytical point 18, 1  mm outward to the rim) has increasing X_Sps and X_Alm and decreasing X_Pyr and X_Grs. The compositional zoning in segment I is considered as growth zoning and that in Segment II as diffusive retrograde zoning. Garnet growth zoning records a P–T  path prior to the peak granulite metamorphism. The minimum P – T  conditions are estimated to be 1.35  GPa and 850  °C for peak metamorphism, based on the highest Mg/(Fe+Mg) composition in the garnet (analytical point 18) and matrix hypersthene, biotite and plagioclase. A symplectitic corona surrounds the porphyroblast and appears to have formed at 0.6  GPa and 700  °C. The well-preserved growth zoning in garnet suggests a short residence time for the granulite at peak metamorphism and thus rapid tectonic uplift history. The P–T  path is consistent with that of ultra-high-pressure eclogite in the area. Tectonic movements during a collisional event could have brought both the granulite and the eclogite to their present positions.     

Petrochemical constraints for dual origin of garnet peridotites from the Dabie-Sulu UHP terrane, eastern-central China

Garnet peridotites occur as lenses, blocks or layers within granulite–amphibolite facies gneiss in the Dabie-Sulu ultra-high-pressure (UHP) terrane and contain coesite-bearing eclogite. Two distinct types of garnet peridotite were identified based on mode of occurrence and petrochemical characteristics. Type A mantle-derived peridotites originated from either: (1) the mantle wedge above a subduction zone, (2) the footwall mantle of the subducted slab, or (3) were ancient mantle fragments emplaced at crustal depths prior to UHP metamorphism, whereas type B crustal peridotite and pyroxenite are a portion of mafic–ultramafic complexes that were intruded into the continental crust as magmas prior to subduction. Most type A peridotites were derived from a depleted mantle and exhibit petrochemical characteristics of mantle rocks; however, Sr and Nd isotope compositions of some peridotites have been modified by crustal contamination during subduction and/or exhumation. Type B peridotite and pyroxenite show cumulate structure, and some have experienced crustal metasomatism and contamination documented by high ⁸⁷Sr/⁸⁶Sr ratios (0.707–0.708), low ε_Nd( t ) values (−6 to −9) and low δ¹⁸O values of minerals (+2.92 to +4.52). Garnet peridotites of both types experienced multi-stage recrystallization; some of them record prograde histories. High- P–T  estimates (760–970 °C and 4.0–6.5±0.2 GPa) of peak metamorphism indicate that both mantle-derived and crustal ultramafic rocks were subducted to profound depths >100 km (the deepest may be ≥180–200 km) and experienced UHP metamorphism in a subduction zone with an extremely low geothermal gradient of <5 °C km⁻¹.     

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.     

Steady-diffusion modelling of a reaction zone between a metamorphosed basic dyke and a marble from Hirao-dai, Fukuoka, Japan

A reaction zone between a metamorphosed basic dyke and marble at Hirao-dai, north Kyushu, Japan, consists of well-organized sequential zones of diopside, garnet and wollastonite; textures are characteristic of diffusion-controlled structures. The reaction zone formed during contact metamorphism associated with intrusion of a Cretaceous granodiorite at ∼300 MPa and 700 °C. The metamorphosed basic dyke consists of diopside, biotite and plagioclase ( X _Ab = 0.4–0.8), whereas the marble is almost pure calcite. The initial boundary between the dyke and the marble is probably located within the current diopside zone, as calcite occurs as remnants among diopside grains in areas close to the boundary with the garnet zone. This observation provides a criterion to judge the stability of the zonal sequence in our modelling. The formation of the reaction zone is attributed to a single-stage steady-state process with five overstepping reactions. CaO, MgO, FeO, SiO₂ and AlO_3/2 are the reaction-controlling components that are necessary to describe the growth of the reaction zone. An isochemical steady-diffusion model cannot reproduce the measured phase ratios of product minerals; this indicates open-system behaviour of the reaction zone. The choice of closure components is an essential task in the treatment of open-system modelling, together with determination of phase ratios (Ashworth & Birdi model) or estimation of boundary fluxes (Johnson & Carlson model). Of all the possible combinations of closure components, closure conditions for CaO and MgO provide the best results for both models. The stability of the zonal sequence is limited at relatively large values of L _SiSi/ L _CaCa. Similar results from the two models confirm their consistency under the same closure conditions.     

Calculated mineral equilibria for eclogites in CaO–Na2O–FeO–MgO–Al2O3–SiO2–H2O: application to the Pouébo Terrane, Pam Peninsula, New Caledonia

The high- P , medium- T  Pouébo terrane of the Pam Peninsula, northern New Caledonia includes barroisite- and glaucophane-bearing eclogite and variably rehydrated equivalents. The metamorphic evolution of the Pouébo terrane is inferred from calculated P–T  and P–T  – X H2O pseudosections for bulk compositions appropriate to these rocks in the model system CaO–Na₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O. The eclogites experienced a clockwise P–T  path that reached P ≈19  kbar and T  ≈600  °C. The eclogitic mineral assemblages are preserved because reaction consequent upon decompression consumed the rocks' fluid. Extensive reaction occurred only in rocks with fluid influx during decompression of the Pouébo terrane.     

Carbonate-hosted talc deposits in the contact aureole of an igneous intrusion (Hwanggangri mineralized zone,South Korea): geochemistry,phase relationships,and stable isotope studies

Many talc deposits occur in the Hwanggangri Mineralized Zone (HMZ) in dolomitic marbles of the Cambro-Ordovician Samtaesan Formation within 1 km of the contact with the Cretaceous Muamsa Granite. Talc commonly forms fine-grained, fibrous aggregates, or pseudomorphs after tremolite; abundant tremolite is included as impurities in the talc ore. Talc generally was derived from tremolite in calc-silicate rock within the dolomitic marble. Calc-silicate rock, consisting mainly of tremolite and diopside, was generated from silicic metasomatism during the prograde stage, which promoted decarbonation reactions until dolomite was exhausted locally. Hydrothermal alteration of calc-silicate rock to talc is marked by the addition of Mg and Si, and the leaching of Ca; Cr, Co, and Ni were relatively immobile during the retrograde stage. Contact metamorphism related to the granite intrusion generated the successive appearance of tremolite, diopside, and forsterite, or wollastonite-bearing assemblages in the marble, depending on the bulk rock composition. The X_CO2 content of the metamorphic fluids rose initially above X_CO2=0.6, and decreased steadily toward a water-rich composition with increasing temperature above 600 °C in the calcitic marble, while buffered reaction of the dolomitic marble occurred at higher X_CO2 conditions above 600 °C. Talc mineralization developed under metastable conditions with infiltration of large amounts of igneous fluids along a fault-shattered zone during the retrograde stage and is characterized by the loss of Ca²⁺ with the addition of Mg²⁺. Oxygen and carbon isotopic variations of carbonate and calc-silicate minerals are in agreement with theoretical relationships determined for decarbonation products of contact metamorphism. Talc formation temperatures obtained from oxygen isotope fractionation, T–X_CO2 relationships, and activity diagrams range from 380 to 400 °C.     

Timing and exhumation of eclogite facies shear zones, Musgrave Block, central Australia

Timing constraints on shear zones can provide an insight into the kinematic and exhumation evolution of metamorphic belts. In the Musgrave Block, central Australia, granulite facies gneisses have been affected, to varying degrees, by mylonitic deformation, some of which attained eclogite facies. The Davenport Shear Zone is a dominant strike-slip system that formed at eclogite facies conditions ( T  ≈650  °C and P ≈12.0  kbar). Sm–Nd mineral isochrons obtained from equilibrated high-pressure assemblages, as well as ⁴⁰Ar–³⁹Ar data, show that the eclogite and greenschist facies high-strain overprints were coeval, at c .  550  Ma. Mylonitic processes do not appear to have reset the U–Pb system in zircon, but may have partially disturbed it. The thermal gradient in the Musgrave Block crust at c .  550  Ma was c .  16  °C  km⁻¹ and at c .  535  Ma was c .  18  °C  km⁻¹, based on P – T  estimates of eclogite and greenschist facies shear zones, respectively. These estimates are similar to present-day geothermal gradients in many stable continental shield areas, suggesting that the region did not undergo a significant transient perturbation of the geotherm. Therefore, in the Musgrave Block, cooling subsequent to eclogite facies metamorphism appears to have been controlled by exhumation, rather than by the removal of a heat source. Estimated exhumation rates in the range 0.2 to ≥1.5  mm year⁻¹ are comparable with other orogenic belts, rather than cratonic areas elsewhere.     

Fluid-rock history of granulite facies humite-marbles from Ambasamudram, southern India.

An extensive humite‐bearing marble horizon within a supracrustal sequence at Ambasamudram, southern India, was studied using petrological and stable isotopic techniques to define its metamorphic history and fluid characteristics. At peak metamorphic temperatures of 775±73°C, based on calcite‐graphite carbon isotope thermometry, the mineral assemblages suggest layer‐by‐layer control of fluid compositions. Clinohumite + calcite‐bearing assemblages suggest X_CO2 < 0.4 (at 700°C and 5 kbar), calcite + forsterite + K‐feldspar‐bearing assemblages suggest X_CO2>0.9 (at 790°C); and local wollastonite + scapolite + grossular‐bearing zones formed at X_CO2 of c. 0.3. Retrograde reaction textures such as scapolite + quartz symplectites after feldspar and calcite and replacement of dolomite + diopside or tremolite+dolomite after calcite+forsterite or calcite+clinohumite are indicative of retrogression under high X_CO2 conditions. Calcite preserves late Proterozoic carbon and oxygen isotopic signatures and the marble lacks evidence for extensive retrograde fluid infiltration, while during prograde metamorphism the possible infiltration of aqueous fluids did not produce significant isotopic resetting. Isotopic zonation of calcite and graphite grains was likely produced by localized CO₂ fluid infiltration during retrogression. Contrary to the widespread occurrence of humite‐marbles related to retrograde aqueous fluid infiltration, the Ambasamudram humite‐marbles record a prograde‐to‐peak metamorphic humite formation and retrogression under conditions of low X_H2O.     

韩国春川软玉的矿物学研究

采用常规宝石学测试、偏光显微镜观察与电子探针(EPMA)分析对具有矿化分带的韩国春川软玉进行研究。结果表明,春川软玉主要矿物组成为透闪石,其次有透辉石、方解石、白云石、滑石等。矿化分带分为大理岩带、蚀变带、软玉+蚀变带、软玉带,是白云质大理岩经过多次交代与变质作用形成的。     

The Fluid Evolution Related to Talc Mineralization in the Hwanggangri Area, South Korea

Abstract: Scores of talc deposits distributed in the Hwanggangri Mineralized Zone, South Korea are interpreted to have resulted from the contact metamorphic process related to the igneous intrusion of the Muamsa Granite. Talc usually occurs as an alteration product from tremolite, which is crystallized during the prograde stage. It commonly forms fine–grained, fibrous aggregates, or pseudomorphs after tremolite, and abundant tremolite is included as impurities in the talc ore. Quantitative X-ray diffraction analysis has shown that the ores can be divided into three types depending on the concentrations of talc; talc-tremolite ore (talc > 50 %), tremolite-talc ore (10 % < talc < 50 %), and tremolite (talc < 10 %) ores. Oxygen isotope compositions of those talc ores become higher from 10.9–12.1 through 11.6–12.3 to 11.9–13.2% with increasing tremolite concentrations, while hydrogen isotope compositions are not so variable, –73 to –69%. The high value of the calculated δ¹⁸O_H2O of the fluids equilibrated with the tremolite may have resulted from the mixing of magmatic water with ¹⁸O–enriched CO₂ evolved from the decarbonation reaction during the prograde stage. However, as the decarbonation reaction ceased during the retrograde stage, the inferred oxygen isotope compositions of talc-forming fluids show similar values to those of the igneous fluids.     

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).     

Cr-rich magnesiochloritoid eclogites from the Monviso ophiolites (Western Alps, Italy)

Cr-rich magnesiochloritoid in the eclogitized ophiolites of the Monviso massif occurs in the least differentiated rocks of the gabbroic sequence (troctolites to melatroctolites). Chloritoid ( X _Mg=0.63–0.85; Cr≤0.55, atoms) co-exists with omphacite, talc and garnet. Minor, syn-eclogitic minerals are chromite, rutile and sometimes magnesite and Cr–Ti oxides.
Coronitic textures, indicative of a static recrystallization, characterize the analysed samples. Layers of variable mineral composition develop among igneous plagioclase, olivine, clinopyroxene and spinel. The minerals in the coronitic layers display sharp compositional zonings. The igneous minerals are commonly not preserved; their presence in the original assemblage is inferred from the mineralogical composition of the pseudomorphs.
Syn-eclogitic volatile components are indicated by the development of OH-bearing minerals (e.g. chloritoid & talc) and carbonates (e.g. magnesite), and supported by the presence of coarse-grained and fibrous mineral growths. The complex pseudomorphic replacements of igneous minerals suggest that these rocks changed their mineralogical composition prior to the eclogite facies recrystallization, most likely during ocean-floor metamorphism. It is suggested that syn-eclogitic fluids formed by breakdown reactions of pre-eclogitic volatile-bearing minerals.
Geothermobarometry indicates that the investigated rocks recrystallized at a depth corresponding to 2.4  GPa and temperatures of 620±50  °C. The attainment of high-pressure conditions is supported by the presence of magnesiochloritoid, magnesite and garnet with high pyrope content (up to 58  mol%). P–T  estimates point to a very low thermal gradient (about 9  °C km⁻¹), comparable to that deduced in the adjacent Dora-Maira ultra-high pressure unit.     

Metamorphic evolution of the Naga Hills eclogite and blueschist, Northeast India: implications for early subduction of the Indian plate under the Burma microplate

Tectonic slices and lenses of eclogite within mafic and ultramafic rocks of the Early Cretaceous–Eocene Naga Hills ophiolite were studied to constrain the physical conditions of eastward subduction of the Indian plate under the Burma microplate and convergence rate prior to the India–Eurasia collision. Some of the lenses are composed of eclogite, garnet-blueschist, glaucophanite and greenschist from core to margin, representing a retrograde hydrothermal alteration sequence. Barroisite, garnet, omphacite and epidote with minor chlorite, phengite, rutile and quartz constitute the peak metamorphic assemblage. In eclogite and garnet-blueschist, garnet shows an increase in Mg and Fe and decrease in Mn from core to rim. In chlorite in eclogite, Mg increases from core to rim. Inclusions of epidote, glaucophane, omphacite and quartz in garnet represent the pre-peak assemblage. Glaucophane also occurs profusely at the rims of barroisite. The matrix glaucophane and epidote represent the post-peak assemblage. The Fe³⁺ content of garnet-hosted omphacite is higher than that of matrix omphacite, and Fe³⁺ increases from core to rim in matrix glaucophane. Albite occurs in late stage veins. P – T pseudosection analysis indicates that the Naga Hills eclogites followed a clockwise P – T path with prograde metamorphism beginning at ∼1.3 GPa/525 °C and peaking at 1.7–2.0 GPa/580–610 °C, and subsequent retrogression to ∼1.1 GPa/540 °C. A comparison of these P – T conditions with numerical thermal models of plate subduction indicates that the Naga Hills eclogites probably formed near the top of the subducting crust with convergence rates of ∼ 55–100 km Myr⁻¹, consistent with high pre-collision convergence rates between India and Eurasia.     

Hot contacts of garnet peridotites in middle/upper crustal levels: new constraints on the nature of the late Variscan high-T/low-P event in the Moldanubian (Central Vosges/NE France)

P–T  paths based on parageneses in the immediate vicinity of former high-temperature contact zones between mantle peridotites and granulitic country rocks of the Central Vosges (NE France) were derived by applying several conventional thermometers and thermobarometric calculations with an internally consistent dataset. The results indicate that former garnet peridotites and garnet–spinel peridotites were welded together with crustal rocks at depths corresponding to 1–1.2 GPa. The temperature of the crustal rocks was about 650–700 °C at this stage, whereas values of 1100 °C (garnet peridotites) and 800–900 °C (garnet–spinel peridotites) were calculated for the ultramafic rocks. After emplacement of the mantle rocks, exhumation of the lower crust took place to a depth corresponding to 0.2–0.3 GPa. The temperatures of the incorporated peridotite slices were still high (900–1000 °C) at this stage. This is indicated by the presence of high- T  /low- P parageneses ( c . 800 °C, 0.2–0.3 GPa) in a small (1–10 m) contact aureole around a former garnet peridotite. Crustal rocks distant to the peridotites equilibrated in the same pressure range at lower temperature (650–700 °C). High cooling rates (10²–10³ °C Ma⁻¹) were calculated for a garnet–biotite rock inclusion in the peridotites and for the crustal rocks at the contact by applying garnet–biotite diffusion modelling. Minimum rates of 0.75–7.5 cm a⁻¹ are required for vertical ascent of rock units (30 km vertical distance) derived from the crust–mantle boundary, resulting in a late Variscan (340 Ma) high- T  /low- P event.     

Aragonite and magnesite in eclogites from the Jæren nappe,SW Norway: disequilibrium in the system CaCO3–MgCO3 and petrological implications

Eclogites from the Jæren nappe in the Caledonian orogenic belt of SW Norway contain aragonite, magnesite and dolomite in quartz‐rich layers. The carbonates comprise composite grains that occur interstitially between phases of the eclogite facies assemblage: garnet + omphacite + zoisite + clinozoisite + quartz + apatite + rutile ± dolomite ± kyanite ± phengite. Pressure and temperature conditions for the main eclogite stage are estimated to be 2.3–2.8 GPa and 585–655 °C. Published ultrahigh pressure (UHP) experiments on CaO‐, MgO‐ and CO₂‐bearing systems have shown that equilibrium assemblages of aragonite and magnesite form as a result of dolomite breakdown at pressures >5 GPa. As a result, recognition of magnesite and aragonite in eclogite facies rocks has been used as an indicator for UHP conditions. However, petrological testing showed that the samples studied here have not experienced such conditions. Aragonite and magnesite show disequilibrium textures that indicate replacement of magnesite by aragonite. This process is inferred to have occurred via a coupled dissolution–precipitation reaction. The formation of aragonite is constrained to eclogite facies conditions, which implies that the studied rocks have experienced metasomatic, reactive fluid flow during their residence at high pressure (HP) conditions. During decompression, the bimineralic carbonate aggregates were overgrown by rims of dolomite, which partially reacted with aragonite to form Mg‐calcite. The well‐preserved carbonate assemblages and textures observed in the studied samples provide a detailed record of the reaction series that affected the rocks during and after their residence at P–T conditions near the coesite stability field. Recognition of the HP mechanism of magnesite replacement by aragonite provides new insight into metasomatic processes that occur in subduction zones and illustrates how fluids facilitate HP carbonate reactions that do not occur in dry systems at otherwise identical physiochemical conditions. This study documents that caution is warranted in interpreting aragonite‐magnesite associations in eclogite facies rocks as evidence for UHP metamorphic conditions.     

Source of coesite inclusions within inherited magmatic zircon from Sulu UHP rocks, eastern China, and their bearing for fluid–rock interaction and SHRIMP dating

The 5-km deep Chinese Continental Scientific Drilling Main Hole penetrated a sequence of ultrahigh pressure (UHP)-metamorphic rocks consisting mainly of eclogite, gneiss and garnet-peridotite with minor schist and quartzite. Zircon separates taken from thin layers of schist and gneiss within eclogite were investigated. Cathodoluminescence images of zircon grains show that they have oscillatory zoned magmatic cores and unzoned to patchy zoned metamorphic rims. Zircon rims contain rare coesite and calcite inclusions whereas cores contain inclusions of both low- P minerals (e.g. feldspar, biotite and quartz) and coesite and other eclogite-facies minerals such as phengite and jadeite. The zircon cores give highly variable ²⁰⁶Pb/²³⁸U ages ranging from 760 to 431 Ma for schist and from 698 to 285 Ma for gneiss, and relatively high but variable Th/U ratios (0.16–1.91). We suggest that the coesite and other eclogite facies mineral inclusions in zircon cores were not magmatic but formed through metasomatic processes caused by fluids during UHP metamorphism, and that the fluids contain components of SiO₂, Al₂O₃, K₂O, FeO, MgO, Na₂O and H₂O. Metasomatism of the Sulu UHP rocks during continental subduction to mantle depths has partly altered magmatic zircon cores and reset isotopic systems. This study provides key evidence that mineral inclusions within magmatic zircon domains are not unequivocal indicators of the formation conditions of the respective domain. This finding leads us to conclude that the routine procedure for dating of metamorphic events solely based on the occurrence of mineral inclusions in zoned zircon could be misleading and the data should be treated with caution.     

Graphite deformation in marble and mylonitic marble, Grenville Province, Canadian Shield

In the southern Grenville Province of the Canadian Shield (Otter Lake area), high-grade marble, gneiss and amphibolite have been folded about north- to north-east-trending axes; mylonite zones, parallel to layering and 0.1–10  cm wide, are locally present in marble.
In nonmylonitic marble, graphite occurs as c . 1–mm hexagonal prisms, which are commonly accompanied by a relatively few crystals that have been deformed, resulting in cleavage separation and the formation of folds and kink bands. Fracture-filled calcite contains less Mg and Fe than surrounding calcite (e.g. <0.30 compared with 1.8–2.7  wt% MgO, and 0.02–0.12 compared with 0.13–0.18  wt% FeO); the composition of fracture-filled dolomite is similar to that of the surrounding dolomite. In semimylonite, graphite forms elongate streaks of fragmented crystals and, in mylonite, further fragmentation has occurred to produce extremely small particles. The fragmentation has not destroyed the atomic structure (hexagonal modification) of graphite.
The behaviour of biotite was similar to that of graphite, but extreme fragmentation did not occur. Dolomite was more rigid than calcite, and in mylonite it occurs more commonly as relics. Amphibole and pyroxene crystals remained undeformed but are locally replaced by calcite.
The numerous microprocesses that have evidently occurred in marble and mylonitic marble of the study area are: coarsening (calcite, graphite), twinning (calcite, dolomite), slip (calcite, dolomite, graphite, biotite), strain-induced recrystallization (calcite), microfolding and kink-band formation (graphite, biotite), fragmentation (graphite) and the pressure-induced transport of calcite and dolomite to voids in graphite and biotite.     

Partial high-pressure aragonitization of micritic limestones in an accretionary complex, Tavşanlı Zone, NW Turkey

Pelagic micritic limestones within an upper Cretaceous accretionary complex in the Tavşanlı Zone, NW Turkey, preserve textures indicating incomplete prograde transformation of micritic calcite to aragonite, representing the only known example of this type. Aragonitization starts at the central parts of the micritic limestone beds and advances towards the lower and upper parts of the layers at the expense of micrite. Micrite is very fine grained (<0.003 mm) and contains radiolaria, foraminifera and thin shell fragments. Aragonite forms large crystals, up to 3 cm across, with straight grain boundaries and c-axis mostly subparallel to the carbonate beds. Relict micritic portions are devoid of any aragonite grain. Stylolites characterized by the accumulation of clay minerals, Fe-Mn-hydroxides and quartz are concentrated in the upper and lower parts of the beds. Stylolite formation precedes aragonitization. Conditions of aragonitization are estimated as 200 ± 50 °C and 0.45–0.65 GPa, based on metamorphic mineral assemblages observed in associated basalts. Several features such as (i) constant composition of micritic calcite (98–99 mol.% CaCO₃) throughout individual beds, (ii) enormous grain size difference between micritic calcite and aragonite (up to 1200 times), and (iii) absence of any aragonite grains within the relict micritic portions suggest that kinetic rather than thermodynamic factors controlled selective aragonite formation in the central portions of carbonate layers.