Constraints from melt inclusions and their host olivines on the petrogenesis of Oligocene-Early Miocene Xindian basalts, Chifeng area, North China Craton

The geochemical characteristics of melt inclusions and their host olivines provide important information on the processes that create magmas and the nature of their mantle and crustal source regions. We report chemical compositions of melt inclusions, their host olivines and bulk rocks of Xindian basalts in Chifeng area, North China Craton. Compositions of both bulk rocks and melt inclusions are tholeiitic. Based on petrographic observations and compositional variation of melt inclusions, the crystallizing sequence of Xindian basalts is as follows: olivine (at MgO > ~5.5 wt%), plagioclase (beginning at MgO = ~5.5 wt%), clinopyroxene and ilmenite (at MgO < 5.0 wt%). High Ni contents and Fe/Mn ratios, and low Ca and Mn contents in olivine phenocrysts, combining with low CaO contents of relatively high MgO melt inclusions (MgO > 6 wt%), indicate that Xindian basalts are possibly derived from a pyroxenite source rather than a peridotite source. In the CS-MS-A diagram, all the high MgO melt inclusions (MgO > 6.0 wt%) project in the field between garnet + clinopyroxene + liquid and garnet + clinopyroxene + orthopyroxene + liquid near 3.0 GPa, further suggesting that residual minerals are mainly garnet and clinopyroxene, with possible presence of orthopyroxene, but without olivine. Modeling calculations using MELTS show that the water content of Xindian basalts is 0.3–0.7 wt% at MgO = 8.13 wt%. Using 20–25 % of partial melting estimated by moderately incompatible element ratios, the water content in the source of Xindian basalts is inferred to be ≥450 ppm, much higher than 6–85 ppm in dry lithospheric mantle. The melting depth is inferred to be ~3.0 GPa, much deeper than that of tholeiitic lavas (<2.0 GPa), assuming a peridotite source with a normal mantle potential temperature. Such melting depth is virtually equal to the thickness of lithosphere beneath Chifeng area (~100 km), suggesting that Xindian basalts are derived from the asthenospheric mantle, if the lithospheric lid effect model is assumed.     

A garnet–hornblende geothermometer: calibration, testing, and application to the Pelona Schist, Southern California

Abstract A garnet–hornblende Fe–Mg exchange geothermometer has been calibrated against the garnet–clinopyroxene geothermometer of Ellis & Green (1979) using data on coexisting garnet + hornblende + clinopyroxene in amphibolite and granulite facies metamorphic assemblages. Data for the Fe–Mg exchange reaction between garnet and hornblende have been fitted to the equation. In K_D=Δ (X_Ca,g) where K_D is the Fe–Mg distribution coefficient, using a robust regression approach, giving a thermometer of the form: with very satisfactory agreement between garnet–hornblende and garnet–clinopyroxene temperatures. The thermometer is applicable below about 850°C to rocks with Mn-poor garnet and common hornblende of widely varying chemistry metamorphosed at low a_O2. Application of the garnet–hornblende geothermometer to Dalradian garnet amphibolites gives temperatures in good agreement with those predicted by pelite petrogenetic grids, ranging from 520°C for the lower garnet zone to 565–610°C for the staurolite to kyanite zones. These results suggest that systematic errors introduced by closure temperature problems in the application of the garnet–clinopyroxene geothermometer to the ‘calibration’data set are not serious. Application to ‘eclogitic’garnet amphibolites suggests that garnet and hornblende seldom attain Fe–Mg exchange equilibrium in these rocks. Quartzo-feldspathic and mafic schists of the Pelona Schist on Sierra Pelona, Southern California, were metamorphosed under high pressure greenschist, epidote–amphibolite and (oligoclase) amphibolite facies beneath the Vincent Thrust at pressures deduced to be 10±1 kbar using the phengite geobarometer, and 8–9kbar using the jadeite content of clinopyroxene in equilibrium with oligoclase and quartz. Application of the garnet–hornblende thermometer gives temperatures ranging from about 480°C at the garnet isograd through 570°C at the oligoclase isograd to a maximum of 620–650°C near the thrust. Inverted thermal gradients beneath the Vincent Thrust were in the range 170 to 250°C per km close to the thrust.     

Ca-Eskola incorporation in clinopyroxene: limitations and petrological implications for eclogites and related rocks

Clinopyroxene is an essential mineral in eclogitic rocks. It commonly contains minor amounts of the defect-bearing Ca-Eskola (CaEs, Ca_0.5□_0.5AlSi₂O₆) component, with higher concentrations generally considered to indicate a high-pressure origin at least within the coesite stability field. Changes in pressure and temperature conditions can lead to exsolution of this component as a free SiO₂ phase, which may have a number of petrological implications. This makes it important to understand the factors that maximize CaEs incorporation in clinopyroxene. We have undertaken a series of experiments at high pressures and temperatures (4–10 GPa and 1000–1350 °C) to further investigate the systematics of CaEs incorporation in eclogite-like clinopyroxene and the factors responsible for maximizing CaEs contents. Two simple chemical systems were chosen that allow unambiguous interpretation of the results: (1) CMAS + H₂O and (2) two compositions in the NCMAS system. All experimental products contained clinopyroxene and garnet along with either a free SiO₂ phase or a silicate melt. Coexisting garnet is grossular-rich, generally with X _gr ≥ 0.67. Compositional variations are attributable to the presence or absence of melt and changes in modal amounts of garnet at different pressure–temperature conditions. Even small amounts of H₂O lower the solidus temperature and the presence of a melt reduces the SiO₂ activity, which destabilizes the CaEs component in clinopyroxene. The CaEs and the Ca-Tschermaks (CaTs, CaAl₂SiO₆) components in clinopyroxene decrease with increasing jadeite mole fraction, which is also a function of pressure and bulk Al content. Modeling X-ray powder diffraction data yields a molar volume for the CaEs endmember of V _CaEs = 60.87(63) cm³, which reasonably agrees with a literature value that was estimated from natural samples. In the presence of coexisting coesite, the CaEs and CaTs do not vary independently of each other, being controlled by the internal equilibrium 2CaEs = CaTs + 3SiO₂ (coesite). This relation, observed in simple systems (i.e., CMAS ± Na), is also obeyed by clinopyroxene in more complex, natural analog bulk compositions. An assessment of available experimental data reveals a maximum of 15–18 mol% CaEs in eclogitic clinopyroxene at conditions corresponding to 130–180 km depth. CaEs contents are maximized at high temperatures; i.e., at or near the solidus in the presence of coesite. Thus, this study supports the role of CaEs exsolution in contributing to melt generation during upwelling of eclogite bodies in the mantle, albeit with some caveats. Somewhat higher maximum CaEs contents (~20 mol%) are found in Ca and Al-rich bulk compositions, such as grospydite xenoliths. Such bulk compositions also seem to require the coexistence of kyanite. Other Ca and Al-rich rock types, like rodingites, should have the potential of containing CaEs-rich clinopyroxenes, except that they are SiO₂-undersaturated. This emphasizes the further role of bulk composition, in addition to high temperatures, in achieving maximum CaEs contents in high-pressure clinopyroxene.     

Ultrahigh-pressure metamorphism and exhumation of garnet-bearing ultramafic rocks from the Lanterman Range (northern Victoria Land, Antarctica)

Northern Victoria Land is a key area for the Ross Orogen – a Palaeozoic foldbelt formed at the palaeo‐Pacific margin of Gondwana. A narrow and discontinuous high‐ to ultrahigh‐pressure (UHP) belt, consisting of mafic and ultramafic rocks (including garnet‐bearing types) within a metasedimentary sequence of gneisses and quartzites, is exposed at the Lanterman Range (northern Victoria Land). Garnet‐bearing ultramafic rocks evolved through at least six metamorphic stages. Stage 1 is defined by medium‐grained garnet + olivine + low‐Al orthopyroxene + clinopyroxene, whereas finer‐grained garnet + olivine + orthopyroxene + clinopyroxene + amphibole constitutes the stage 2 assemblage. Stage 3 is defined by kelyphites of orthopyroxene + clinopyroxene + spinel ± amphibole around garnet. Porphyroblasts of amphibole replacing garnet and clinopyroxene characterize stage 4. Retrograde stages 5 and 6 consist of tremolite + Mg‐chlorite ± serpentine ± talc. A high‐temperature (～950 °C), spinel‐bearing protolith (stage 0), is identified on the basis of orthopyroxene + clinopyroxene + olivine + spinel + amphibole inclusions within stage 1 garnet. The P–T estimates for stage 1 are indicative of UHP conditions (3.2–3.3 GPa and 764–820 °C), whereas stage 2 is constrained between 726–788 °C and 2.6–2.9 GPa. Stage 3 records a decompression up to 1.1–1.3 GPa at 705–776 °C. Stages 4, 5 and 6 reflect uplift and cooling, the final estimates yielding values below 0.5 GPa at 300–400 °C. The retrograde P–T path is nearly isothermal from UHP conditions up to deep crustal levels, and becomes a cooling–unloading path from intermediate to shallow levels. The garnet‐bearing ultramafic rocks originated in the mantle wedge and were probably incorporated into the subduction zone with felsic and mafic rocks with which they shared the subsequent metamorphic and geodynamic evolution. The density and rheology of the subducted rocks are compatible with detachment of slices along the subduction channel and gravity‐driven exhumation.     

Partial melting of lower crust at 10–15 kbar: constraints on adakite and TTG formation

The pressure–temperature (P–T) conditions for producing adakite/tonalite–trondhjemite–granodiorite (TTG) magmas from lower crust compositions are still open to debate. We have carried out partial melting experiments of mafic lower crust in the piston-cylinder apparatus at 10–15 kbar and 800–1,050 °C to investigate the major and trace elements of melts and residual minerals and further constrain the P–T range appropriate for adakite/TTG formation. The experimental residues include the following: amphibolite (plagioclase + amphibole ± garnet) at 10–15 kbar and 800 °C, garnet granulite (plagioclase + amphibole + garnet + clinopyroxene + orthopyroxene) at 12.5 kbar and 900 °C, two-pyroxene granulite (plagioclase + clinopyroxene + orthopyroxene ± amphibole) at 10 kbar and 900 °C and 10–12.5 kbar and 1,000 °C, garnet pyroxenite (garnet + clinopyroxene ± amphibole) at 13.5–15 kbar and 900–1,000 °C, and pyroxenite (clinopyroxene + orthopyroxene) at 15 kbar and 1,050 °C. The partial melts change from granodiorite to tonalite with increasing melt proportions. Sr enrichment occurs in partial melts in equilibrium with <20 wt% plagioclase, whereas depletions of Ti, Sr, and heavy rare earth elements (HREE) occur relative to the starting material when the amounts of residual amphibole, plagioclase, and garnet are >20 wt%, respectively. Major elements and trace element patterns of partial melts produced by 10–40 wt% melting of lower crust composition at 10–12.5 kbar and 800–900 °C and 15 kbar and 800 °C closely resemble adakite/TTG rocks. TiO₂ contents of the 1,000–1,050 °C melts are higher than that of pristine adakite/TTG. In comparison with natural adakite/TTG, partial melts produced at 10–12.5 kbar and 1,000 °C and 15 kbar and 1,050 °C have elevated HREE, whereas partial melts at 13.5–15 kbar and 900–1,000 °C in equilibrium with >20 wt% garnet have depressed Yb and elevated La/Yb and Gd/Yb. It is suggested that the most appropriate P–T conditions for producing adakite/TTG from mafic lower crust are 800–950 °C and 10–12.5 kbar (corresponding to a depth of 30–40 km), whereas a depth of >45–50 km is unfavorable. Consequently, an overthickened crust and eclogite residue are not necessarily required for producing adakite/TTG from lower crust. The lower crust delamination model, which has been embraced for intra-continental adakite/TTG formation, should be reappraised.     

Decompression and unmixing of crystals included in diamonds from the mantle transition zone

A suite of exceptional mineral inclusions in diamonds from the São Luiz river, Juina province, Brazil, shows a wide range of garnet/majorite mineral compositions co-existing with clinopyroxene; the overall bulk compositions are eclogitic. The inclusions have a wide variety of textural arrangements, but crystallographic data obtained by EBSD shows that each inclusion consists of a single garnet with constant crystallographic orientation whilst clinopyroxene grains have preferred orientation with relation to garnet {110} and <111>. This suggests that the inclusions were originally single phase majoritic garnets, and that they preserve various states of progressive unmixing (exsolution) into lower pressure garnet and clinopyroxene compositions during transport of the host diamonds towards the Earth’s surface. On the basis of high pressure–temperature experimental data some of the original majoritic garnets must have come from depths of 450 km or more, and therefore resided in the transition zone and asthenospheric upper mantle. Particularly extensive re-equilibration of many inclusions took place at depths of ca 180–200 km (probably close to the base of the continental lithosphere). The partially unmixed state of the inclusions provides a unique opportunity for using mineral diffusion data to roughly estimate the rate of transport through the asthenospheric upper mantle, and within error this rate is found to be broadly compatible with expected transport rates by upper mantle convection or plume flow.     

Paleozoic subduction of the southern Dunhuang Orogenic Belt,northwest China: metamorphism and geochronology of the Shuixiakou area

Amphibolites in the Shuixiakou area of the southern Dunhuang Orogenic Belt, southernmost Central Asian Orogenic Belt (CAOB), occur as lenses within hornblende-biotite-plagioclase gneiss or pelitic schist, exhibiting block-in-matrix feature of tectonic mélange. Three generations of metamorphic mineral assemblages (M1, M2, and M3) have been recognized in the garnet-bearing amphibolite lenses. The metamorphic prograde assemblage (M1) is documented with inclusion trails (hornblende + plagioclase + quartz) within garnet porphyroblasts, and are estimated to be formed under 610–690 °C and 6.5–10.2 kbar. The metamorphic peak assemblage (M2) consists of garnet + hornblende + clinopyroxene + plagioclase + quartz in the matrix and records metamorphic peak P-T conditions of 720–750 °C and 13.4–14.7 kbar. The retrograde assemblage (M3) is represented by the symplectic assemblage (hornblende + plagioclase + quartz ± biotite ± magnetite) rimming the garnet porphyroblast, formed in the decompression stage under P-T conditions of 630–730 °C and 3.8–7.2 kbar. The derived metamorphic P-T paths show similar tight clockwise loops including nearly isothermal decompression processes, typical of orogenic metamorphism. SIMS dating of metamorphic zircons from the amphibolites confirm that the high-pressure metamorphism (M2) occurred at ca. 438–398 Ma.     

Internally consistent geothermometers for garnet peridotites and pyroxenites

Mutual relationships among temperatures estimated with the most widely used geothermometers for garnet peridotites and pyroxenites demonstrate that the methods are not internally consistent and may diverge by over 200°C even in well-equilibrated mantle xenoliths. The Taylor (N Jb Min Abh 172:381–408, 1998) two-pyroxene (TA98) and the Nimis and Taylor (Contrib Mineral Petrol 139:541–554, 2000) single-clinopyroxene thermometers are shown to provide the most reliable estimates, as they reproduce the temperatures of experiments in a variety of simple and natural peridotitic systems. Discrepancies between these two thermometers are negligible in applications to a wide variety of natural samples (≤30°C). The Brey and Köhler (J Petrol 31:1353–1378, 1990) Ca-in-Opx thermometer shows good agreement with TA98 in the range 1,000–1,400°C and a positive bias at lower T (up to +90°C, on average, at T _TA98 = 700°C). The popular Brey and Köhler (J Petrol 31:1353–1378, 1990) two-pyroxene thermometer performs well on clinopyroxene with Na contents of ~0.05 atoms per 6-oxygen formula, but shows a systematic positive bias with increasing Na_Cpx (+150°C at Na_Cpx = 0.25). Among Fe–Mg exchange thermometers, the Harley (Contrib Mineral Petrol 86:359–373, 1984) orthopyroxene–garnet and the recent Wu and Zhao (J Metamorphic Geol 25:497–505, 2007) olivine–garnet formulations show the highest precision, but systematically diverge (up to ca. 150°C, on average) from TA98 estimates at T far from 1,100°C and at T < 1,200°C, respectively; these systematic errors are also evident by comparison with experimental data for natural peridotite systems. The older O’Neill and Wood (Contrib Mineral Petrol 70:59–70, 1979) version of the olivine–garnet Fe–Mg thermometer and all popular versions of the clinopyroxene–garnet Fe–Mg thermometer show unacceptably low precision, with discrepancies exceeding 200°C when compared to TA98 results for well-equilibrated xenoliths. Empirical correction to the Brey and Köhler (J Petrol 31:1353–1378, 1990) Ca-in-Opx thermometer and recalibration of the orthopyroxene–garnet thermometer, using well-equilibrated mantle xenoliths and TA98 temperatures as calibrants, are provided in this study to ensure consistency with TA98 estimates in the range 700–1,400°C. Observed discrepancies between the new orthopyroxene–garnet thermometer and TA98 for some localities can be interpreted in the light of orthopyroxene–garnet Fe³⁺ partitioning systematics and suggest localized and lateral variations in mantle redox conditions, in broad agreement with existing oxybarometric data. Kinetic decoupling of Ca–Mg and Fe–Mg exchange equilibria caused by transient heating appears to be common, but not ubiquitous, near the base of the lithosphere.     

Mineral evolution of a garnet-pyroxenite nodule within eclogite, eastern Sulu ultrahigh-pressure metamorphic terrane, East China

Detailed microtextural observations and bulk chemical analysis were undertaken on a garnet‐pyroxenite nodule within retrograde eclogites from the NE Sulu ultrahigh‐pressure metamorphic (UHPM) terrane. The results suggest that the protolith was a cumulate from a gabbroic body. The nodule consists primarily of coarse clinopyroxene grains with a very high content of the Ca‐Tschermakite molecule. Microscopic observations and back‐scattered electron images (BSE) demonstrate a complicated intergrowth of clinopyroxene, garnet and ilmenite, which represents the peak metamorphic assemblage. The primary clinopyroxene grains are armoured with a thin garnet corona up to 0.5 mm wide that forms an interconnected network. Within the clinopyroxene grains, four sets of garnet lamellae are distributed along crystallographic planes; locally, a vermicular intergrowth of garnet and diopside is developed. Besides the garnet, parallel arrays of ilmenite blebs are common within the clinopyroxene. Hydrous minerals such as amphibole, zoisite and titanite formed at later stages, and replaced diopside, garnet and ilmenite respectively. The P–T conditions determined for the formation of the garnet lamellae indicate that the garnet pyroxenite experienced UHP metamorphism at the same peak P–T condition as its host eclogite. The very high Ca‐Tschermakite content (31–34 mol.%) of the primary clinopyroxene indicates crystallization at about 9–17 kbar and 1250–1450 °C, and together with the microtextural observations, suggests that the protolith of the garnet pyroxenite was a cumulate from a former gabbroic body, in which case, the host eclogite might represent the gabbroic body.     

Chronology of the high-pressure metamorphism of Norwegian garnet peridotites/pyroxenites

Eclogite facies mineral assemblages are variably preserved in mafic and ultramafic rocks within the Western Gneiss Region (WGR) of Norway. Mineralogical and microstructural data indicate that some Mg–Cr-rich, Alpine-type peridotites have had a complex metamorphic history. The metamorphic evolution of these rocks has been described in terms of a seven-stage evolutionary model; each stage is characterized by a specific mineral assemblage. Stages II and III both comprise garnet-bearing mineral assemblages. Garnet-bearing assemblages are also present in Fe–Ti-rich peridotites which commonly occur as layers in mafic complexes. Sm–Nd isotopic results are reported for mineral and whole rock samples from both of these types of peridotites and related rocks. The partitioning of Sm and Nd between coexisting garnet and clinopyroxene is used to assess chemical equilibrium. One sample of Mg–Cr-type peridotite shows non-disturbed partitioning of Sm and Nd between Stage II garnet and clinopyroxene pairs and yields a garnet–clinopyroxene–whole-rock date of 1703 ± 29 Ma (I= 0.51069, MSWD = 0.04). This is the best estimate for the age of the Stage II high-P assemblage. Other Stage II garnet–clinopyroxene pairs reflect later disturbance of the Sm–Nd system and yield dates in the range 1303 to 1040 Ma. These dates may not have any geological significance. Stage III garnet–clinopyroxene pairs typically have equilibrated Sm–Nd partitioning and two samples yield dates of 437 ± 58 and 511 ± 18 Ma. This suggests that equilibration of the Stage III high-P assemblage is related to the Caledonian orogeny and is more or less contemporaneous with high-P metamorphism of ‘country-rock’eclogites in the surrounding gneisses. The Sm–Nd mineral data for the Fe–Ti-rich garnet peridotites and for a superferrian eclogite, which occurs as a dyke within the Gurskebotn Mg–Cr-type peridotite, are consistent with a Palaeozoic high-P metamorphism. Finally a synoptic P–T–t path is proposed for the Mg–Cr-type peridotites which is consistent with the petrological and geochronological data.     

Phlogopite in mantle xenoliths and kimberlite from the Grib pipe,Arkhangelsk province,Russia:Evidence for multi-stage mantle metasomatism and origin of phlogopite in kimberlite

We present petrography and mineral chemistry for both phlogopite,from mantle-derived xenoliths(garnet peridotite,eclogite and clinopyroxene-phlogopite rocks)and for megacryst,macrocryst and groundmass flakes from the Grib kimberlite in the Arkhangelsk diamond province of Russia to provide new insights into multi-stage metasomatism in the subcratonic lithospheric mantle(SCLM)and the origin of phlogopite in kimberlite.Based on the analysed xenoliths,phlogopite is characterized by several generations.The first generation(Phil)occurs as coarse,discrete grains within garnet peridotite and eclogite xenoliths and as a rock-forming mineral within clinopyroxene-phlogopite xenoliths.The second phlogopite generation(Phl2)occurs as rims and outer zones that surround the Phil grains and as fine flakes within kimberlite-related veinlets filled with carbonate,serpentine,chlorite and spinel.In garnet peridotite xenoliths,phlogopite occurs as overgrowths surrounding garnet porphyroblasts,within which phlogopite is associated with Cr-spinel and minor carbonate.In eclogite xenoliths,phlogopite occasionally associates with carbonate bearing veinlet networks.Phlogopite,from the kimberlite,occurs as megacrysts,macrocrysts,microcrysts and fine flakes in the groundmass and matrix of kimberlitic pyroclasts.Most phlogopite grains within the kimberlite are characterised by signs of deformation and form partly fragmented grains,which indicates that they are the disintegrated fragments of previously larger grains.Phil,within the garnet peridotite and clinopyroxene-phlogopite xenoliths,is characterised by low Ti and Cr contents(TiO_21 wt.%,Cr_2 O_31 wt.% and Mg# = 100 × Mg/(Mg+ Fe)92)typical of primary peridotite phlogopite in mantle peridotite xenoliths from global kimberlite occurrences.They formed during SCLM metasomatism that led to a transformation from garnet peridotite to clinopyroxene-phlogopite rocks and the crystallisation of phlogopite and high-Cr clinopyroxene megacrysts before the generation of host-kimberlite magmas.One of the possible processes to generate low-Ti-Cr phlogopite is via the replacement of garnet during its interaction with a metasomatic agent enriched in K and H_2O.Rb-Sr isotopic data indicates that the metasomatic agent had a contribution of more radiogenic source than the host-kimberlite magma.Compared with peridotite xenoliths,eclogite xenoliths feature low-Ti phlogopites that are depleted in Cr_2O_3 despite a wider range of TiO_2 concentrations.The presence of phlogopite in eclogite xenoliths indicates that metasomatic processes affected peridotite as well as eclogite within the SCLM beneath the Grib kimberlite.Phl2 has high Ti and Cr concentrations(TiO_22 wt.%,Cr_2O_31 wt.% and Mg# = 100× Mg/(Mg + Fe)92)and compositionally overlaps with phlogopite from polymict brecc:ia xenoliths that occur in global kimberlite formations.These phlogopites are the product of kimberlitic magma and mantle rock interaction at mantle depths where Phl2 overgrew Phil grains or crystallized directly from stalled batches of kimberlitic magmas.Megacrysts,most macrocrysts and microcrysts are disintegrated phlogopite fragments from metasomatised peridotite and eclogite xenoliths.Fine phlogopite flakes within kimberlite groundmass represent mixing of high-Ti-Cr phlogopite antecrysts and high-Ti and low-Cr kimberlitic phlogopite with high Al and Ba contents that may have formed individual grains or overgrown antecrysts.Based on the results of this study,we propose a schematic model of SCLM metasomatism involving phlogopite crystallization,megacryst formation,and genesis of kimberlite magmas as recorded by the Grib pipe.     

Metasomatic parageneses in deep-seated xenoliths from pipes Udachnaya and Komsomol'skaya-Magnitnaya as indicators of fluid transfer through the mantle lithosphere of the Siberian craton

The petrography, major element, and trace element (TE) compositions of minerals from two types of modal metasomatites (metasomatized peridotites and pyroxenites) from kimberlite pipes Udachnaya and Komsomol'skaya-Magnitnaya, Yakutia, have been studied. It is shown that texturally and chemically equilibrated metasomatites A consist of a set of superimposed minerals: phlogopite + diopside ± ilmenite ± apatite ± sulfides ± graphite. Their major and trace element compositions have specific features. The contents of TEs in garnet and clinopyroxene from these metasomatites are close to those in garnet and clinopyroxene from low-temperature coarse-grained peridotites richest in TEs. The distribution of a significant portion of TEs between garnet and clinopyroxene from A-type metasomatites and from coarse-grained lherzolites rich in TEs is close to experimental values reported for minerals coexisting with carbonatitic and basaltic fluids. We assume that this metasomatic process was nearly synchronous with the global metamorphism and cratonization of the mantle lithosphere and that high-density silicate–carbonate fluidmelts were metasomatizing agents.Another large mantle metasomatism process in the lithosphere of the Siberian craton was associated with the Middle Paleozoic kimberlite magmatic event, induced by the Yakutian thermochemical plume. Metasomatic minerals (Mg phlogopite + Cr diopside + chromite ± sulfides ± graphite) intensely replaced the minerals of the primary paragenesis, particularly, garnet. These reaction metasomatites show a sine-shaped REE pattern in garnet and disequilibrium between garnet and clinopyroxene. It is supposed that the reaction metasomatism in the mantle lithosphere of the Siberian craton was associated with ingress of reduced asthenospheric fluids at early stages of the kimberlite formation cycle. Metasomatic graphite formed in metasomatites of both types, and this fact evidences for two diamond formation epochs in the history of the mantle lithosphere of the Siberian craton.     

Separate or shared metamorphic histories of eclogites and surrounding rocks? An example from the Bohemian Massif

Eclogite boudins occur within an orthogneiss sheet enclosed in a Barrovian metapelite‐dominated volcano‐sedimentary sequence within the Velké Vrbno unit, NE Bohemian Massif. A metamorphic and lithological break defines the base of the eclogite‐bearing orthogneiss nappe, with a structurally lower sequence without eclogite exposed in a tectonic window. The typical assemblage of the structurally upper metapelites is garnet–staurolite–kyanite–biotite–plagioclase–muscovite–quartz–ilmenite ± rutile ± silli‐manite and prograde‐zoned garnet includes chloritoid–chlorite–paragonite–margarite, staurolite–chlorite–paragonite–margarite and kyanite–chlorite–rutile. In pseudosection modelling in the system Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O (NCKFMASH) using THERMOCALC, the prograde path crosses the discontinuous reaction chloritoid + margarite = chlorite + garnet + staurolite + paragonite (with muscovite + quartz + H₂O) at 9.5 kbar and 570 °C and the metamorphic peak is reached at 11 kbar and 640 °C. Decompression through about 7 kbar is indicated by sillimanite and biotite growing at the expense of garnet. In the tectonic window, the structurally lower metapelites (garnet–staurolite–biotite–muscovite–quartz ± plagioclase ± sillimanite ± kyanite) and amphibolites (garnet–amphibole–plagioclase ± epidote) indicate a metamorphic peak of 10 kbar at 620 °C and 11 kbar and 610–660 °C, respectively, that is consistent with the other metapelites. The eclogites are composed of garnet, omphacite relicts (jadeite = 33%) within plagioclase–clinopyroxene symplectites, epidote and late amphibole–plagioclase domains. Garnet commonly includes rutile–quartz–epidote ± clinopyroxene (jadeite = 43%) ± magnetite ± amphibole and its growth zoning is compatible in the pseudosection with burial under H₂O‐undersaturated conditions to 18 kbar and 680 °C. Plagioclase + amphibole replaces garnet within foliated boudin margins and results in the assemblage epidote–amphibole–plagioclase indicating that decompression occurred under decreasing temperature into garnet‐free epidote–amphibolite facies conditions. The prograde path of eclogites and metapelites up to the metamorphic peak cannot be shared, being along different geothermal gradients, of about 11 and 17 °C km^?1, respectively, to metamorphic pressure peaks that are 6–7 kbar apart. The eclogite–orthogneiss sheet docked with metapelites at about 11 kbar and 650 °C, and from this depth the exhumation of the pile is shared.     

Garnet–clinopyroxene intermediate granulites in the St. Leonhard massif of the Bohemian Massif: ultrahigh‐temperature metamorphism at high pressure or not?

Garnet–clinopyroxene intermediate granulites occur as thin layers within garnet–kyanite–K–feldspar felsic granulites of the St. Leonhard granulite body in the Bohemian Massif. They consist of several domains. One domain consists of coarser‐grained coexisting ternary feldspar, clinopyroxene, garnet, quartz and accessory rutile and zircon. The garnet has 16–20% grossular, and the clinopyroxene has 9% jadeite and contains orthopyroxene exsolution lamellae. Reintegrated ternary feldspar and the Zr‐in‐rutile thermometer give temperatures higher than 950 °C. Mineral equilibria modelling suggests crystallization at 14 kbar. The occurrence and preservation of this mineral assemblage is consistent with crystallization from hot dry melt. Between these domains is a finer‐grained deformed matrix made up of diopsidic clinopyroxene, orthopyroxene, plagioclase and K‐feldspar, apparently produced by reworking of the coarser‐grained domains. Embedded in this matrix, and pre‐dating the reworking deformation, are garnet porphyroblasts that contain clinopyroxene, feldspar, quartz, rutile and zircon inclusions. In contrast with the garnet in the coarser‐grained domains, the garnet generally has >30% grossular, the included clinopyroxene has 7–27% jadeite and the Zr content of rutile indicates much lower temperatures. Some of these high‐grossular garnet show zoning in Fe/(Fe + Mg), decreasing from 0.7 in the core to 0.6 and then increasing to 0.7 at the rim. These garnet are enigmatic, but with reference to appropriate pseudosections are consistent with localized new mineral growth from 650 to 850 °C and 10 to 17 kbar, or with equilibration at 20 kbar and 770 °C, modified by two‐stage diffusional re‐equilibration of rims, at 10–15 and 8 kbar. The strong pervasive deformation has obscured relationships that might have aided the interpretation of the origin of these porphyroblasts. The evolution of these rocks is consistent with formation by igneous crystallization and subsequent metamorphism to high‐T and high‐P, rather than an origin by ultrahigh‐T metamorphism. Regarding the petrographic complexity, combination of the high grossular garnet with the ternary feldspar to infer ultrahigh‐T metamorphism at high pressure is not justified.     

Partial melting of secondary pyroxenite at 1 and 1.5 GPa,and its role in upwelling heterogeneous mantle

We performed partial melting experiments at 1 and 1.5 GPa, and 1180–1400 °C, to investigate the melting under mantle conditions of an olivine-websterite (GV10), which represents a natural proxy of secondary (or stage 2) pyroxenite. Its subsolidus mineralogy consists of clinopyroxene, orthopyroxene, olivine and spinel (+garnet at 1.5 GPa). Solidus temperature is located between 1180 and 1200 °C at 1 GPa, and between 1230 and 1250 °C at 1.5 GPa. Orthopyroxene (±garnet), spinel and clinopyroxene are progressively consumed by melting reactions to produce olivine and melt. High coefficient of orthopyroxene in the melting reaction results in relatively high SiO₂ content of low melt fractions. After orthopyroxene exhaustion, melt composition is controlled by the composition of coexisting clinopyroxene. At increasing melt fraction, CaO content of melt increases, whereas Na₂O, Al₂O₃ and TiO₂ behave as incompatible elements. Low Na₂O contents reflect high partition coefficient of Na between clinopyroxene and melt (\(D_{{{\text{Na}}_{ 2} {\text{O}}}}^{{{\text{cpx}}/{\text{liquid}}}}\)). Melting of GV10 produces Quartz- to Hyperstene-normative basaltic melts that differ from peridotitic melts only in terms of lower Na₂O and higher CaO contents. We model the partial melting of mantle sources made of different mixing of secondary pyroxenite and fertile lherzolite in the context of adiabatic oceanic mantle upwelling. At low potential temperatures (T _P < 1310 °C), low-degree melt fractions from secondary pyroxenite react with surrounding peridotite producing orthopyroxene-rich reaction zones (or refertilized peridotite) and refractory clinopyroxene-rich residues. At higher T _P (1310–1430 °C), simultaneous melting of pyroxenite and peridotite produces mixed melts with major element compositions matching those of primitive MORBs. This reinforces the notion that secondary pyroxenite may be potential hidden components in MORB mantle source.     

The influence of Fe<Superscript>3+</Superscript> on garnet–orthopyroxene and garnet–olivine geothermometers

Applying Fe²⁺–Mg exchange geothermometers to natural samples may lead to incorrect temperature estimates if significant Fe³⁺ is present. In order to quantify this effect, high-pressure experiments were carried out in a belt apparatus in a natural system close to CFMAS at 5 GPa and 1,100–1,400 °C. The oxygen fugacity in the experiments was at or below the Re–ReO₂ buffer. This is at significantly more oxidized conditions than in previous experiments, and, as consequence, higher Fe³⁺/Fe²⁺ ratios were generated. The Fe³⁺ content of garnet in the experiments was quantified by electron microprobe using the flank method. Making the usual assumption that Fe_total = Fe²⁺, the two-pyroxene thermometer of Brey and Köhler (J Pet 31:1353–1378, 1990) reproduced the experimental temperature to ±35 °C and the garnet–clinopyroxene Fe²⁺–Mg exchange thermometer of Krogh (Contrib Miner Pet 99:44–48, 1988) overestimated the temperatures on average by only 25 °C. On the other hand, application of the garnet–olivine (O’Neill and Wood in Contrib Miner Pet 70:59–70, 1979) and garnet–orthopyroxene (Harley in Contrib Miner Pet 86:359–373, 1984) exchange geothermometers yielded an underestimation in calculated temperatures of >200 °C. However, making explicit accounting for Fe³⁺ in garnet (i.e. using only measured Fe²⁺) leads to a vast improvement in the agreement between calculated and experimental temperatures, generally to within ±70 °C for the garnet–orthopyroxene geothermometer as well as noticeable improvement of calculated temperatures for the garnet–olivine geothermometer. Our results demonstrate that the two-pyroxene and garnet–clinopyroxene thermometers are rather insensitive to the presence of Fe³⁺ whilst direct accounting of Fe³⁺ in garnet is essential when applying the garnet–olivine and garnet–orthopyroxene thermometers.     

Tectonic implications of garnet-bearing mantle xenoliths exhumed by Quaternary magmatism in the Hangay dome, central Mongolia

Garnet-bearing mantle xenoliths have been recovered from Quaternary alkali basalts, both within and peripheral to the Hangay dome of central Mongolia. Microfabric analysis and thermobaromery, combining empirical thermobarometers and the self-consistent dataset of THERMOCALC, indicate that garnet websterites from the Shavaryn-Tsaram volcanic centre at the dome core were formed in the spinel-lherzolite upper mantle at pressures of 17–18 kbars and temperatures of 1,070–1,090°C, whereas garnet lherzolites were derived from greater depths (18–20 kbars). Garnet lherzolites from the Baga Togo Uul vents near the dome edge were formed at 18–22 kbars under significantly cooler conditions (960–1,000°C). These xenoliths reveal reaction coronas of (1) orthopyroxene, clinopyroxene, plagioclase and spinel mantling garnets; (2) spongy rims of olivine replacing orthopyroxene and (3) low-Na, low-Al clinopyroxene replacing primary clinopyroxene. Trace-element abundances indicate that clinopyroxene from these coronas is in chemical equilibrium with the host magma. The thermobarometric and textural data suggest that lherzolite xenoliths from both sites were derived from depths of 60–70 km and entrained in magma at 1,200–1,300°C. The average rate of ascent, as determined by olivine zoning, lies in the range 0.2–0.3 m s⁻¹. The contrast in thermal profiles of the upper mantle between the two sites is consistent with a mantle plume beneath the Hangay dome with elevated thermal conditions beneath the core of the dome being comparable to estimates of the Pleistocene geotherm beneath the Baikal rift.     

Phlogopite- and clinopyroxene-dominated fractional crystallization of an alkaline primitive melt: petrology and mineral chemistry of the Dariv Igneous Complex,Western Mongolia

We present field relationships, petrography, and mineral major and trace element data for the Neoproterozoic Dariv Igneous Complex of the Altaids of Western Mongolia. This unique complex of high-K plutonic rocks is composed of well-exposed, km-scale igneous intrusions of wehrlites, phlogopite wehrlites, apatite-bearing phlogopite clinopyroxenites, monzogabbros, monzodiorites, and clinopyroxene-bearing monzonites, all of which are intruded by late stage lamprophyric and aplitic dikes. The biotite-dominated igneous complex intrudes depleted harzburgitic serpentinite. The observed lithological variability and petrographic observations suggest that the plutonic rocks can be ascribed to a fractionation sequence defined by olivine + clinopyroxene ± Fe–Ti oxides → phlogopite + apatite → K-feldspar + plagioclase → amphibole + quartz. Notably, phlogopite is the dominant hydrous mafic mineral. Petrogenesis of the observed lithologies through a common fractionation sequence is supported by a gradual decrease in the Mg# [molar Mg/(Fe_total + Mg) × 100] of mafic minerals. Crystallization conditions are derived from experimental phase petrology and mineral chemistry. The most primitive ultramafic cumulates crystallized at ≤0.5 GPa and 1,210–1,100 °C and oxygen fugacity (fO₂) of +2–3 ?FMQ (log units above the fayalite–quartz–magnetite buffer). Trace element modeling using clinopyroxene and apatite rare earth element compositions indicates that the dominant mechanism of differentiation was fractional crystallization. The trace element composition of a parental melt was calculated from primitive clinopyroxene compositions and compares favorably with the compositions of syn-magmatic lamprophyres that crosscut the fractionation sequence. The parental melt composition is highly enriched in Th, U, large ion lithophile elements, and light rare earth elements and has a pronounced negative Nb–Ta depletion, suggestive of an alkaline primitive melt originating from a subduction-imprinted mantle. Comparison with a global compilation of primitive arc melts demonstrates that Dariv primitive melts are similar in composition to high-K primitive melts found in some continental arcs. Thus, the high-K fractionation sequence exposed in the Dariv Igneous Complex may be a previously unrecognized important fractionation sequence resulting in alkali-rich upper crustal granitoids in continental arc settings.     

Fe–Mg interdiffusion rates in clinopyroxene: experimental data and implications for Fe–Mg exchange geothermometers

Chemical interdiffusion of Fe–Mg along the c-axis [001] in natural diopside crystals (X _Di = 0.93) was experimentally studied at ambient pressure, at temperatures ranging from 800 to 1,200 °C and oxygen fugacities from 10^?11 to 10^?17 bar. Diffusion couples were prepared by ablating an olivine (X _Fo = 0.3) target to deposit a thin film (20–100 nm) onto a polished surface of a natural, oriented diopside crystal using the pulsed laser deposition technique. After diffusion anneals, compositional depth profiles at the near surface region (~400 nm) were measured using Rutherford backscattering spectroscopy. In the experimental temperature and compositional range, no strong dependence of D ^Fe–Mg on composition of clinopyroxene (Fe/Mg ratio between Di₉₃–Di₆₅) or oxygen fugacity could be detected within the resolution of the study. The lack of fO₂-dependence may be related to the relatively high Al content of the crystals used in this study. Diffusion coefficients, D ^Fe–Mg, can be described by a single Arrhenius relation with $$D^{{{\text{Fe}} - {\text{Mg}}}} = 2. 7 7\pm 4. 2 7\times 10^{ - 7} {\text{exp(}}-3 20. 7\pm 1 6.0{\text{ kJ}}/{\text{mol}}/{\text{RT)m}}^{ 2} /{\text{s}}.$$ D ^Fe–Mg in clinopyroxene appears to be faster than diffusion involving Ca-species (e.g., D ^Ca–Mg) while it is slower than D ^Fe–Mg in other common mafic minerals (spinel, olivine, garnet, and orthopyroxene). As a consequence, diffusion in clinopyroxene may be the rate-limiting process for the freezing of many geothermometers, and compositional zoning in clinopyroxene may preserve records of a higher (compared to that preserved in other coexisting mafic minerals) temperature segment of the thermal history of a rock. In the absence of pervasive recrystallization, clinopyroxene grains will retain compositions from peak temperatures at their cores in most geological and planetary settings where peak temperatures did not exceed ~1,100 °C (e.g., resetting may be expected in slowly cooled mantle rocks, many plutonic mafic rocks, or ultra-high temperature metamorphic rocks).     

Eclogites in the Makuti gneisses of Zimbabwe: implications for the tectonic evolution of the Zambezi Belt in southern Africa

The gneisses of the Makuti Group in north-west Zimbabwe are characterized by complex geometries that resulted from intense non-coaxial deformation in a crustal scale high-strain zone that accommodated extensional deformation along the axis of the Zambezi Belt at c. 800 Ma. Within low-strain domains in the Makuti gneisses, undeformed metagabbroic lenses preserve eclogite and granulite facies assemblages, which record a part of the metamorphic history that predates Pan-African events. Eclogitic rocks can be subdivided into: (1) corona-textured metagabbros that preserve igneous textures, and (2) garnet–omphacite rocks in which primary textures are destroyed. The lenses of eclogitic rocks are enveloped in a mantle of garnet–clinopyroxene–hornblende gneiss, which is a common rock type in the Makuti gneisses. The eclogites preserve multi-staged, domainal, symplectic reaction textures that developed progressively as the rocks experienced loading followed by decompression–heating. In the metagabbros, the original clinopyroxene, plagioclase and olivine domains acted separately during the peak of metamorphism, with plagioclase being replaced by garnet and kyanite, and olivine being replaced by orthopyroxene and possibly omphacite. The peak assemblage was overprinted by: (1) the multi-mineralic corona assemblage pargasite–orthopyroxene–spinel–plagioclase replacing garnet–kyanite–clinopyroxene (possibly at c. 19 kbar, 760±25 °C); (2) orthopyroxene–pargasite–plagioclase–scapolite coronas replacing orthopyroxene (15±1.5 kbar, 750±50 °C); and (3) moats of orthopyroxene–plagioclase replacing garnet (10±1 kbar, 760±50 °C). The garnet–omphacite rocks record similar peak conditions (15±1.1 kbar, 760±60 °C). Garnet–clinopyroxene–hornblende–plagioclase gneisses envelop the eclogites and record matrix conditions of 11±1.5 kbar at 730±50 °C using assemblages that are oriented in the regional fabric. These rocks are characterized by decompression-heating textures, reflecting temperature increases during exhumation of the Makuti gneisses. The eclogite facies rocks formed during a collisional event prior to 850 Ma. Their formation could be related to a suture zone that developed along the axis of the Zambezi Belt during the formation of Rodinia (between 1400 and 850 Ma). The main deformation-metamorphism in the Makuti gneisses occurred around 800 Ma and involved extension and exhumation of the high-P rocks (break-up of Rodinia), which experienced a high-T metamorphic overprint. Around 550–500 Ma, a collisional event associated with the formation of Gondwana resulted in renewed burial and metamorphic recrystallization of the Makuti gneisses.