High-grade regional metamorphism of ultramafic and mafic rocks from the Archaean Sargur terrane,Karnataka, South India

Deformed and metamorphic ultramafic to mafic rocks emplaced into the Archaean Sargur supracrustal series (>3.0 Ga) in Karnataka, southern India, represent layered igneous bodies. The terrane has been affected by several episodes of deformation and metamorphism in the time span from 3.4 to 2.5 Ga ago.During the regional metamorphism about 2.5 Ga ago the igneous bodies re-equilibrated partly or completely at conditions of the upper amphibolite to granulite facies. The development of sagvandites with enstatite + magnesite and anthophyllite + magnesite-bearing assemblages, and of mafic garnet—pyroxene charnockites indicates the presence of CO₂-rich intergranular fluids (X_CO2 ? 0.5) in these rocks during metamorphism.The physical conditions of metamorphism have been estimated by applying methods of geothermobarometry to the recrystallized ultramafic assemblages with olivine, pyroxenes and spinel and to the charnockitic assemblages with garnet, pyroxenes, plagioclase and quartz. A best temperature estimate of 700 ± 30°C was derived with the geothermometers of Evans and Frost (Ol—Spi), Fabriès (Ol—Spi), Wells (Opx—Cpx), Powell (Opx—Cpx), Ellis and Green (Gra—Cpx), Lal and Raith (Gra—Opx), and Danckwerth and Newton (Al₂O₃-content in opx). A mean pressure estimate of 8.6 ± 0.8 kbar has been obtained with the models of Perkins and Newton (Gar—Opx/Cpx—Plag—Qtz). The P—T data indicate a minimum crustal thickness of about 35 km at c. 2.5 Ga in this part of the South Indian Archaean craton.     

Petrogenesis of garnet-bearing ultramafic rocks and associated eclogites in the Su-Lu ultrahigh-P metamorphic terrane, eastern China

Ultramafic blocks that themselves contain eclogite lenses in the Triassic Su-Lu ultrahigh-P terrane of eastern China range in size from hundreds of metres to kilometres. The ultramafic blocks are enclosed in quartzofeldspathic gneiss of early Proterozoic age. Ultramafic rocks include garnetiferous lherzolite, wehrlite, pyroxenite, and hornblende peridotite. Garnet lherzolites are relatively depleted in Al₂O₃ (<3.8wt%), CaO (<3.2%) and TiO₂ (<0.11 wt%), and are low in total REE contents (several p.p.m.), suggesting that the rocks are residual mantle material that was subjected to low degrees of partial melting. The eclogite lenses or layers within the ultramafic rocks are characterized by higher MgO and CaO, lower Al₂O₃ and TiO₂ contents, and a higher CaO/Al₂O₃ ratio compared to eclogites enclosed in the quartzofeldspathic gneiss. Scatter in the plots of major and trace elements vs. MgO, REE patterns and La, Sm and Lu contents suggest that some eclogites were derived from melts formed by various degrees (0.05–0.20) of partial melting of peridotite, and that other eclogites formed by accumulation of garnet and clinopyroxene ± trapped melt in the upper mantle. Both ultramafic and eclogitic rocks have experienced a complex metamorphic history. At least six stages of recrystallization occurred in the ultramafic rocks based on an analysis of reaction textures and mineral compositions. Stage I is a high temperature protolith assemblage of Ol + Opx + Cpx + Spl. Stage II consists of the ultrahigh-pressure assemblage Ol + Cpx + Opx + Grt. Stage III is manifested by the appearance of fine-grained garnet after coarse-grained garnet. Stage IV is characterized by formation of kelyphitic rims of fibrous Opx and Cpx around garnet, and replacement of garnet by spinel and pargasitic-hornblende. Stage V is represented by the assemblage Ol + Opx + Prg-Hbl + Spl. The mineral assemblages of stages VI_A and VI_B are Ol + Tr-Amp + Chl and Serp + Chl ± talc, respectively. Garnet and orthopyroxene all show a decrease in MgO with retrogressive recrystallization and Na₂O in clinopyroxene also decreases throughout this history. Eclogites enclosed within ultramafic blocks consist of Grt + Omp + Rt ± Qtz ± Phn. A few quartz-bearing eclogites contain rounded and oval inclusion of polycrystalline quartz aggregates after coesite in garnet and omphacite. Minor retrograde features include thin symplectic rims or secondary amphiboles after Cpx, and ilmenite after rutile. P-T estimates indicate that the ultrahigh-metamorphism (stage II) of ultramafic rocks occurred at 820-900d? C and 36-41 kbar and that peak metamorphism of eclogites occurred at 730-900d? C and >28 kbar. Consonant with earlier plate tectonic models, we suggest that these rocks were underplated at the base of the continental crust. The rocks then underwent ultrahigh-pressure metamorphism and were tectonically emplaced into thickened continental crust during the Triassic collision between the Sino-Korean and Yangtze cratons.     

A petrogenetic grid for aluminous granulite facies metapelites in the KFMASH system

Due to the retrograde cation exchange problems experienced by conventional geothermobarometers above their closure temperatures, petrogenetic grids are a potentially powerful alternative to unravelling the P–T evolution of ultrahigh‐T granulite terranes. A new qualitative KFMASH (K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O) petrogenetic grid for Mg–Al rich metapelites containing K‐feldspar, sillimanite and quartzofeldspathic melt that successfully accounts for the majority of assemblages composed of variations of sapphirine, spinel, garnet, orthopyroxene, cordierite, biotite and quartz is developed. Univariant reactions are predicted utilizing a newly derived ‘melt projection’ and these reactions are entirely consistent with algebraically calculated reaction coefficients obtained using a set of standard phase compositions. Based upon observations of commonly associated mineral assemblages in natural lithologies the [Spr, Spl], [Qtz, Spl], [Bt, Spl], [Opx, Spr], [Opx, Qtz] and [Bt, Opx] invariant points are assumed to be stable, whilst the [Grt, Spr], [Grt, Qtz], [Spr, Qtz] and [Crd, Qtz] are assumed to be metastable. Biotite‐bearing assemblages are confined to the lowest temperatures, and sapphirine + quartz to the highest temperatures. Orthopyroxene + sillimanite ± quartz assemblages are confined to the highest pressures, whilst spinel‐bearing assemblages are stabilized by lower pressures. The alternative choice of invariant point stability leads to significant differences between this grid and previously proposed topologies. Spinel cannot be stable along with the orthopyroxene and sillimanite assemblage as previously proposed. Further, more subtle differences in topology result from the treatment of H₂O in the chemographic projection used to deduce univariant reactions, and projecting from a water‐bearing quartzofeldspathic melt does not yield the same reaction coefficients as projection from H₂O. The new grid allows reinterpretation of previously proposed evolutionary P–T paths for Mg–Al rich granulites from the Napier Complex and Rauer Group, East Antarctica, and In Ouzzal, Algeria.     

An example of ultrahigh-temperature metamorphism: orthopyroxene–sillimanite–garnet, sapphirine–quartz and spinel–quartz parageneses in Al–Mg granulites from In Hihaou, In Ouzzal, Hoggar

Quartz Al–Mg granulites exposed at In Hihaou, In Ouzzal (NW Hoggar), preserve an unusual high-grade mineral association stable at temperatures up to 1050°C, involving the parageneses orthopyroxene–sillimanite–garnet–quartz, sapphirine–quartz and spinel–quartz. The phase relationships within the FMAS system show that a continuum exists between the earlier prograde reaction textures and those of the later decompressive event. The following mineral reactions involving sillimanite are deduced: (1) Grt+Qtz→Opx+Sil, (2) Opx+Sil→Grt+Spr+Qtz, (3) Grt+Sil+Qtz→Crd, (4) Grt+Sil→Crd+Spr, (5) Grt+Sil+Spr→Crd+Spl, (6) Grt+Sil→Crd+Spl, (7) Grt+Crd+Sil→Spl+Qtz and (8) Grt+Sil→Spl+Qtz. Minerals in quartz Al–Mg granulites display compositional variations consistent with the observed reactions. The Mg/(Mg+Fe²⁺) range of the main minerals is as follows: cordierite (0.81–0.97), sapphirine (0.77–0.88), orthopyroxene (0.65–0.81), garnet (0.33–0.64) and spinel (0.23–0.56). The reaction textures and the evolution of the mineral assemblages in the quartz Al–Mg granulites indicate a clockwise P–T trajectory characterized by peak conditions of at least 10 kbar and 1050°C, followed by decompression from 10 to 6 kbar at a temperature of at least 900°C.     

Metamorphic history of high-pressure granulites in Payer Land, Greenland Caledonides

A high‐P granulite facies gneiss complex occurs in north‐west Payer Land (74°28′?74°47′N) in the central part of the East Greenland Caledonian (Ordovician–Devonian) orogen. High‐P metamorphism of the Payer Land gneiss complex resulted in formation of the assemblages Grt + Cpx + Amp + Qtz + Ru ± Pl in mafic rocks, and Grt + Ol + Cpx + Opx + Spl in rare ultramafic pods. Associated metapelites experienced anatexis in the kyanite stability field. Peak metamorphic assemblages formed around 800–850 °C at pressures of c. 1.4–1.7 GPa, corresponding to crustal depths of c. 50 km. Mafic granulites contain abundant reaction textures, including the replacement of garnet by symplectites of Opx + Spl + Pl, indicating that the high‐P event was followed by decompression while the granulites remained at elevated temperatures. Charnockitic gneisses from Payer Land show evidence of late Archean (c. 2.8–2.4 Ga) crustal growth and subsequent Palaeoproterozoic (c. 1.85 Ga) metamorphism. The gneiss complex experienced intense reworking during the Caledonian continental collision. On the basis of Caledonian monazite ages recorded from the high‐P anatectic metapelites, the clockwise P–T evolution and formation of the high‐P granulite facies assemblages is related to Caledonian crustal thickening, which resulted in formation of eclogites approximately 300 km north of Payer Land. The Payer Land granulites comprise a metamorphic core complex, which is separated from the overlying low‐grade supracrustal rocks (the Neoproterozoic Eleonore Bay Supergroup) by a late Caledonian extensional fault zone, the Payer Land Detachment. The steep, nearly isothermal, unloading P–T path recorded by the granulites can be explained by erosional and tectonic unroofing along the Payer Land Detachment.     

Two-stage decompression in garnet-bearing mafic granulites from Sostrene Island, Prydz Bay, East Antarctica

Mafic garnet-bearing granulites from Sostrene Island, 150 km southwest of Davis Station on the coast of Prydz Bay, East Antarctica, exhibit two-stage symplectic coronas on garnet, formed after peak metamorphic conditions (M1). An outer corona of Opx (Mg₆₆) + Pl (An_94–97) + minor Hbl mantles a finer-grained inner corona of Opx (Mg₆₇) + Pl (An_95–96) + Spl (Mg₃₆). Both symplectites contain minor ilmenite–magnetite intergrowths. The finer-grained symplectite also occurs along a fracture cleavage in the garnet. The outer corona originated during a second metamorphic event (M2) via the reaction Grt + Cpx (Hbl) + SiO₂= Opx + Pl (1), whereas the inner corona formed later in response to decompression and minor deformation, resulting in the fracture cleavage in the garnet, according to the reaction Grt = Opx + Pl + Spl (2). The grossular content of the garent (X_Grs= 0.168) is almost exactly that which is required for the stoichiometric breakdown by reaction (2) (calculated X_Grs= 0.167). The mafic rocks are silica undersaturated, and the SiO₂ for reaction (1) was most probably derived externally from the surrounding felsic gneisses. Preferred P–T estimates for M1 based on garnet core (Prp₄₀Alm₄₂Grs₁₇Sps₁)–matrix Opx–Cpx–Hbl pairs are c. 10 kbar at 980°C. The fine-grained symplectite formed post-peak M2 at c. 7 kbar and 850°C. The enclosing felsic gneisses yield pressure estimates of between 5 and 7 kbar, which compare with conditions of c. 6 kbar and 775°C in the nearby Bolingen Islands. These lower P–T estimates are considered to be representative of the widespread 1100-Ma metamorphic event recognized in outcrops along the Prydz Bay coast. The high-P, high-T estimates derived from the garnet relics provide evidence for an earlier, possibly Archaean, high-grade metamorphic event.     

Modeling of deep-seated high-alumina parageneses on the basis of the stability fields of corundum- and spinel-normative assemblages of the system CaO–MgO–Al2O3–SiO2

To elaborate physicochemical models for the origin of crystalline rocks, experimental studies of the field of high-alumina assemblages of the system CaO–MgO–Al₂O₃–SiO₂ were carried out at 10–30 kbar and 1250–1535 °C. We have determined the phase relations between the melt (L) and An, Sp, Cpx, Cor, and Ga, the slope of the rays of the monovariant reactions An + Sp = Cpx + Cor + (Ga) and L = Cpx +Ga + Cor + Sp, the position of the nonvariant point (An, Sp, Cpx, Cor, Ga, L), and the compositions of phases participating in these reactions. Based on a topological analysis of the studied segment of the system CaO–MgO–Al₂O₃–SiO₂, we have substantiated that “eclogitization” must follow the reaction Opx + An + Sp = Cpx + Ga. A fundamental continuous series of eutectic monovariant equilibria was observed: L = Cpx + Opx + Fo + An, L = Cpx + Opx + An + Sp, L = Cpx (+ Ga) + An + Sp, and L = Cpx + Cor (+ Ga) + An. A change in the melt composition in this series of eutectic reactions depending on pressure must reflect the most likely magma genesis trend in nature. Comparision of the composition fields in which the above series of reactions is observed with the composition fields of the rocks of magmatic formations showed that this series is most similar to the alkali-earth series of rocks. The mineralogical compositions of cumulates and phenocrysts found in the effusive and dike varieties of these rocks correspond to unique sets of subsolidus phase associations and individual subsolidus phases crystallizing in this fundamental eutectic series.     

Reworking of deep-seated gabbros and associated contact metamorphosed paragneisses in the southeastern part of the Seiland Igneous Province, northern Norway

The Seiland Igneous Province of the North Norwegian Caledonides consists of a suite of deep-seated rift-related magmatic rocks emplaced into paragneisses during late Precambrian to Ordovician time. In the south-eastern part of the province, contact metamorphism of the paragneisses and later reworking of intrusives and associated contact aureoles have resulted in the development of three successive metamorphic stages. The contact metamorphic assemblage (M1) Opx + Grt + Qtz + Pl + Kfs + Hc + Ilm ± Crd is preserved in xenolithic rafts of paragneiss within metagabbro. Geothermobarometric calculations yield 930-960d? C and 5-6.5 kbar for the contact metamorphism. M1 was followed by cooling, accompanied by strong shearing, formation of the gneiss foliation and recrystallization at intermediate-P granulite facies conditions (M2). Stable M2 phases are Cpx + Opx + Pl +Ilm ± Hbl in metagabbro and Grt ± Sil ± Opx + Kfs + Qtz + Pl ± Bt + Ilm in host paragneiss. The M2 conditions are estimated to 700-750d? C and 5-7 kbar. A subsequent pressure increase is recorded in the M3 episode, which is associated with recrystallization in narrow ductile shear zones and secondary growth on M2 minerals. M3 is defined by the assemblages Grt + Cpx ± Opx + Pl + Ru + Qtz in metagabbro, and Grt ± Ky + Qtz + Pl ± Kfs + Bt + Ru in host paragneiss. M3 conditions are estimated to 650-700d? C and 8-10 kbar. The substantial pressure increase related to the M2 → M3 transition is interpreted to be a result of (early?) Caledonian overthrusting. Chemical zoning in cordierite and biotite suggest rapid cooling following the M3 event. The proposed P-T-t evolution implies that the tectonic evolution of the Seiland Igneous Province was long (at least 330 Ma) and complex and involved initial rifting and extension followed by crustal thickening and compression.     

Opx–Cpx exsolution textures in lherzolites of the Cretaceous Purang Ophiolite (S. Tibet,China), and the deep mantle origin of Neotethyan abyssal peridotites

ABSTRACT

We investigated lherzolitic peridotites in the Cretaceous Purang ophiolite along the Yarlung Zhangbo suture zone (YZSZ) in SW Tibet to constrain their mantle–melt evolution history. Coarse-grained Purang lherzolites contain orthopyroxene (Opx) and olivine (Ol) porphyroclasts with embayments filled by small olivine (Ol) neoblasts. Both clinopyroxene (Cpx) and Opx display exsolution textures represented by lamellae structures. Opx exsolution (Opx1) in clinopyroxene (Cpx1) is made of enstatite, whose compositions (Al₂O₃ = 3.85–4.90 wt%, CaO = <3.77 wt%, Cr₂O₃ = 0.85–3.82 wt%) are characteristic of abyssal peridotites. Host clinopyroxenes (Cpx1) have higher Mg#s and Na₂O, with lower TiO₂ and Al₂O₃ contents than Cpx2 exsolution lamellae in Opx, and show variable LREE patterns. Pyroxene compositions of the lherzolites indicate 10–15% partial melting of a fertile mantle protolith. P–T estimates (1.3–2.3 GPa, 745–1067°C) and the trace element chemistry of pyroxenes with exsolution textures suggest crystallization depths of ~75 km in the upper mantle, where the original pyroxenes became decomposed, forming exsolved structures. Further upwelling of lherzolites into shallow depths in the mantle resulted in crystal–plastic deformation of the exsolved pyroxenes. Combined with the occurrence of microdiamond and ultrahigh-pressure (UHP) mineral inclusions in chromites of the Purang peridotites, the pyroxene exsolution textures reported here confirm a multi-stage partial melting history of the Purang lherzolites and at least three discrete stages of P-T conditions in the course of their upwelling through the mantle during their intra-oceanic evolution.     

Experimental Study on the Solubility of Cr^2 in Olivine,Orthopyroxene and Spinel Solid Solutions

Experiments have been performed on the system MgO-SiO2-Cr-O at 0-2.88 GPa and 1100-1450℃,focusing on the stability of Cr^2 in olivine(O1),orthopyroxene(Opx) and spinel(Sp) and its partitioning between these phases.Analytical reagent grade chemicals,MgO,SiO2,Cr2O3.and Cr were used to make starting mixtures.Excess Cr(50%) was then added in these mixtures to ensure that the resultant phases were in equilibrium with the metal Cr.Flux of BaO B2O3(%) was added for facilitating experimental equilibrium and crystal growth.Cr was used as capsule material.All phases in the product were identified by X-ray and analyzed by electron microprobe,The contents of CrO in the different phases(O1,Opx and Sp)were calculated according to stoichiometry.The obtained results of calculation indicate that Cr^3 in Ol and Opx is negligible.The experimental results show;(a) with increasing temperature and decreasing pressure,Cr^2 solubility in Ol,Opx and Sp increases;(b) with in creasing temperature,the partitioning coefficient of Mg and Cr^2 between Ol and Opx decreases,that between Opx and Sp increases,and that between Ol and Sp remains almost unchanged;(c) the effect of pressure on all partitioning coefficients is negligible.     

Liquid compositions from low-pressure experimental melting of pelitic rock from Morton Pass, Wyoming, USA

Low‐pressure crystal‐liquid equilibria in pelitic compositions are important in the formation of low‐pressure, high‐temperature migmatites and in the crystallization of peraluminous leucogranites and S‐type granites and their volcanic equivalents. This paper provides data from vapour‐present melting of cordierite‐bearing pelitic assemblages and augments published data from vapour‐present and vapour‐absent melting of peraluminous compositions, much of which is at higher pressures. Starting material for the experiments was a pelitic rock from Morton Pass, Wyoming, with the major assemblage quartz‐K feldspar‐biotite‐cordierite, approximately in the system KFMASH. A greater range in starting materials was obtained by addition of quartz and sillimanite to aliquots of this rock. Sixty‐one experiments were carried out in cold‐seal apparatus at pressures of 1–3.5 kbar (particularly 2 kbar) and temperatures from 700 to 840 °C, with and without the addition of water. In the vapour‐present liquidus relations at 2 kbar near the beginning of melting, the sequence of reactions with increasing temperature is: Qtz + Kfs + Crd + Sil + Spl + V = L; Qtz + Kfs + Crd + Spl + Ilm + V = Bt + L; and Qtz + Bt + V = Crd + Opx + Ilm + L. Vapour‐absent melting starts at about 800 °C with a reaction of the form Qtz + Bt = Kfs + Crd + Opx + Ilm + L. Between approximately 1–3 kbar the congruent melting reaction is biotite‐absent, and biotite is produced by incongruent melting, in contrast to higher‐pressure equilibria. Low pressure melts from pelitic compositions are dominated by Qtz‐Kfs‐Crd. Glasses at 820–840 °C have calculated modes of approximately Qtz₄₂Kfs₄₆Crd₁₂. Granites or granitic leucosomes with more than 10–15% cordierite should be suspected of containing residual cordierite. The low‐pressure glasses are quite similar to the higher‐pressure glasses from the literature. However, X_Mg increases from about 0.1–0.3 with increasing pressure from 1 to 10 kbar, and the low‐temperature low‐pressure glasses are the most Fe‐rich of all the experimental glasses from pelitic compositions.     

Partial melting and the formation of granulite facies assemblages in Namaqualand, South Africa

Abstract Dehydration-melting reactions, in which water from a hydrous phase enters the melt, leaving an anhydrous solid assemblage, are the dominant mechanism of partial melting of high-grade rocks in the absence of externally derived vapour. Equilibria involving melt and solid phases are effective buffers of aH₂,o. The element-partitioning observed in natural rocks suggests that dehydration melting occurs over a temperature interval during which, for most cases, aH₂o is driven to lower values. The mass balance of dehydration melting in typical biotite gneiss and metapelite shows that the proportion of melt in the product assemblage at T± 850°C is relatively small (10–20%), and probably insufficient to mobilize a partially melted rock body. Granulite facies metapelite, biotite gneiss and metabasic gneiss in Namaqualand contain coarse-grained, discordant, unfoliated, anhydrous segregations, surrounded by a finer grained, foliated matrix that commonly includes hydrous minerals. The segregations have modes consistent with the hypothesis that they are the solid and liquid products of the dehydration-melting reactions: Bt + Sil + Qtz + PI = Grt ° Crd + Kfs + L (metapelite), Bt + Qtz + Pl = Opx + Kfs + L (biotite gneiss), and Hbl + Qtz = Opx + Cpx + Pl + L (metabasic gneiss). The size, shape, distribution and modes of segregations suggest only limited migration and extraction of melt. Growth of anhydrous poikiloblasts in matrix regions, development of anhydrous haloes around segregations and formation of dehydrated margins on metabasic layers enclosed in migmatitic metapelites all imply local gradients in water activity. Also, they suggest that individual segregations and bodies of partially melted rock acted as sinks for soluble volatiles. The preservation of anhydrous assemblages and the restricted distribution of late hydrous minerals suggest that retrograde reaction between hydrous melt and solids did not occur and that H₂O in the melt was released as vapour on crystallization. This model, combined with the natural observations, suggests that it is possible to form granulite facies assemblages without participation of external fluid and without major extraction of silicate melt.     

Melt-producing and melt-consuming reactions in the Achankovil cordierite gneisses, South India

Migmatitic cordierite gneisses within the Achankovil Zone (AZ) of southern Pan‐African India record melt‐producing and subsequent melt‐consuming mineral reactions. Early mineral assemblages Bt‐Sil‐Qtz and Bt‐Sil‐Spl, deduced from inclusion textures in garnet prophyroblasts, break down via successive dehydration melting reactions to high‐T phase assemblages (e.g. Grt‐Crd‐Liq, Opx‐Liq, Spl‐Crd‐Liq). Later back reactions between the restite and the in situ crystallizing melt resulted in thin cordierite coronas separating garnet from the leucosome, and partial resorption of garnet to Opx‐Crd or Crd‐Bt‐Qtz symplectites. Leucosomes generally display a moderate (low‐strain gneisses) to strong (high‐strain gneisses) depletion of alkali feldspar attributed to mineral‐melt back reactions partly controlled by the degree of melt segregation. Using a KFMASH partial petrogenetic grid that includes a melt phase, and qualitative pseudosections for microdomains of high and low Al/Si ratios, the successive phase assemblages and reaction textures are interpreted in terms of a clockwise P–T path culminating at about 6–7 kbar and 900–950 °C. This P–T path is consistent with, but more detailed than published results, which suggests that taking a melt phase into account is not only a valid, but also a useful approach. Comparing P–T data and lithological and isotopic data for the AZ with adjacent East Gondwana fragments, suggests the presence of a coherent metasedimentary unit exposed from southern Madagascar via South India (AZ) and Sri Lanka (Wanni Complex) to the Lützow–Holm Bay in Eastern Antarctica.     

滇东南马关木厂新生代玄武岩中橄榄岩包体的含水性

对来自滇东南马关木厂的尖晶石二辉橄榄岩中名义上无水矿物(NAMs)进行显微傅里叶变换红外光谱(Micro-FTIR)分析,结果显示,单斜辉石、斜方辉石和橄榄石中均含有以羟基形式存在的结构水,单斜辉石的水含量为160×10~(-6)~557×10~(-6)(质量分数,下同),斜方辉石的水含量为85×10~(-6)~207×10~(-6),橄榄石的水含量为5×10~(-6)~12×10~(-6),根据矿物百分比含量估算的全岩水含量为46×10~(-6)~137×10~(-6);元素地球化学特征表明,本次研究的橄榄岩包体是岩石圈地幔经历较低程度部分熔融的残余;低(La/Yb)N值(0.22~0.57)以及高Ti/Eu比值(4 076~6 772)暗示橄榄岩可能经历了以硅酸盐熔体为交代介质的微弱地幔交代作用;单斜辉石的微量元素组成比较单一,整体表现出高场强元素、大离子亲石元素以及轻稀土元素的同步亏损;结合中国东部地区已经发表的橄榄岩包体含水量数据来看,滇东南马关木厂岩石圈地幔具有明显富水的特征,可能与该区自中生代以来遭受的新特提斯洋壳大规模俯冲流体交代作用有关;与华北克拉通含水量的明显差异有可能反映的是两地岩石圈地幔正处于不同的演化阶段。     

High-temperature metamorphic imprint on calc-silicate granulites of Rayagada,Eastern Ghats,India: implication for the isobaric cooling path

 Calc-silicate granulites from Rayagada, north-central sector of Eastern Ghats granulite belt show a wide range of mineral assemblages and chemical compositions, which can be grouped as Gr. I (grossular- rich garnet-wollastonite-scapolite-calcite-clinopyroxene), Gr. II (andradite-rich garnet-scapolite-calcite-clinopyr- oxene), and Gr. III (scapolite-calcite-clinopyroxene-plagioclase) assemblages. Petrographic features suggest the following several reactions in the CaO–Al₂O₃–SiO₂-vapor system: Mei+4Wo+Cal=3Grs+Qtz +2CO₂, Mei+3Wo+2Cal=3Grs+CO₂, Mei= 3An+Cal, Wo+CO₂=Cal+Qtz, Mei+5Wo =3Grs+2Qtz+CO₂, An+Wo=Grs+Qtz, Mei+ 5Cal+3Qtz=3Grs+6CO₂, and the following reactions in the CaO–FeO–MgO–Al₂O₃–SiO₂-vapor system: Cpx_ss+Scp+Wo=Grt_ss+Qtz+CO₂, 4Hd+ 2Cal+O₂=2Adr+2Qtz+2CO₂, Cpx_ss+Scp= Grt_ss+Cal+Qtz. These reactions have been used to estimate peak T-X _CO2 condition for these granulites. A maximum temperature of ∼920 °C has been calculated at an estimated pressure of 9 kbar. A T-X _CO2 diagram shows an isobaric cooling from ∼920 °C to ∼815 °C. A range of X _CO2 (0.50 at 920 °C to 0.25 at 815 °C) has been observed for Gr. I calc-silicate granulites based on the reaction sequences including coronal garnet-forming reactions. This sequence is suggestive of internal fluid buffering rather than external fluid influx and the differences in X _CO2 conditions has been thought to be due to local buffering of fluid phases. Group II and Gr. III calc-silicate granulites, on the other hand, exhibit relatively lower temperature conditions. Received: 11 September 1995/Accepted: 20 June 1996     

超高温变质作用：以华北内蒙古土贵乌拉地区为例

超高温麻粒岩(富Mg-Al)是指温度高于900℃、压力为0.7~1.3GPa条件下形成的麻粒岩相变质岩,它记录了下地壳超高温极端变质作用的地质信息。富Mg-Al典型超高温矿物组合有:假蓝宝石+石英,尖晶石+石英,大隅石+石榴石,斜方辉石+夕线石+石英,高氟黑云母和钙镁闪石,刚玉+石英。目前世界上发现的超高温麻粒岩带(块)地区有非洲阿尔及利亚、南非、东南极、巴西中部、澳大利亚中部、印度南部和东南部等地。我们在华北克拉通北部内蒙古中南部地区孔兹岩区中发现了超高温麻粒岩,岩性主要为灰黑色条带状夕线石榴黑云片麻岩,其中含有尖晶石+石英、假蓝宝石+石英、斜方辉石+夕线石+石英以及刚玉+尖晶石+石榴石等超高温矿物组合,指示温度达1000℃,压力超过1.0GPa的变质作用。独居石定年获得了(1927±11)Ma以及(1819±11)Ma两个峰期年龄,代表变质年龄。华北克拉通北部超高温麻粒岩的发现对研究华北克拉通与哥伦比亚超大陆的演化关系有重要意义。     

The assemblage orthopyroxene+cummingtonite+quartz. The low-temperature stability limit

The monovariant reaction Opx+H₂O Cum+Ol+Q and the Cum+Opx+Q stability field were studied under hydrothermal conditions at P _total=2940, 4900 bar and the oxygen fugacity of the QFM buffer. Under these conditions, the Opx lower stability brackets were 730°±10° and 740°±5° C, respectively. The kinetics of the reactions in the Cum+ Opx+Q mixture showed that there were only minor differences in the equilibrium compositions of the coexisting Opx and Cum over the 740°–780° C range. At T=780°, 760° and 740° C, the FeO/FeO+MgO ratio, in mol% was: Opx_52.5–Cum_49.5, Opx₆₂–Cum₅₇, Opx₇₂–Cum₆₆ (P=2940 bar) and Opx₆₂–Cum_58.5 Opx_71.5–Cum_66.5, Opx₈₀–Cum₇₅ (P= 4900 bar). The results are in good agreement with earlier studies in the Opx+Ol+Q and Cum+Ol+Q assemblages.Abbreviations Opx Orthopyroxene - Ol olivine - Cum cummingtonite - Mt magnetite - Q quartz - tk talc     

Oriented growth of garnet by topotactic reactions and epitaxy in high‐pressure,mafic garnet granulite formed by dehydration melting of metastable hornblende‐gabbronorite (Jijal Complex,Kohistan Complex,north Pakistan)

Garnet growth in high‐pressure, mafic garnet granulites formed by dehydration melting of hornblende‐gabbronorite protoliths in the Jijal complex (Kohistan palaeo‐island arc complex, north Pakistan) was investigated through a microstructural EBSD‐SEM and HRTEM study. Composite samples preserve a sharp transition in which the low‐pressure precursor is replaced by garnet through a millimetre‐sized reaction front. A magmatic foliation in the gabbronorite is defined by mafic‐rich layering, with an associated magmatic lineation defined by the shape‐preferred orientation (SPO) of mafic clusters composed of orthopyroxene (Opx), clinopyroxene (Cpx), amphibole (Amp) and oxides. The shape of the reaction front is convoluted and oblique to the magmatic layering. Opx, Amp and, to a lesser extent, Cpx show a strong lattice‐preferred orientation (LPO) characterized by an alignment of [001] axes parallel to the magmatic lineation in the precursor hornblende‐gabbronorite. Product garnet (Grt) also displays a strong LPO. Two of the four 〈111〉 axes are within the magmatic foliation plane and the density maximum is subparallel to the precursor magmatic lineation. The crystallographic relationship 〈111〉_Grt // [001]_Opx,Cpx,Amp deduced from the LPO was confirmed by TEM observations. The sharp and discontinuous modal and compositional variations observed at the reaction front attest to the kinetic inhibition of prograde solid‐state reactions predicted by equilibrium‐phase diagrams. The P–T field for the equilibration of Jijal garnet granulites shows that the reaction affinities are 5–10 kJ mol.^?1 for the Grt‐in reaction and 0–5 kJ mol.^?1 for the Opx‐out reaction. Petrographic and textural observations indicate that garnet first nucleated on amphibole at the rims of mafic clusters; this topotactic replacement resulted in a strong LPO of garnet. Once the amphibole was consumed in the reaction, the parallelism of [001] axes of the mafic‐phase reactants favoured the growth of garnet crystals with similar orientations over a pyroxene substrate. These aggregates eventually sintered into single‐crystal garnet. In the absence of deformation, the orientation of mafic precursor phases conditioned the nucleation site and the crystallographic orientation of garnet because of topotaxial transformation reactions and homoepitaxial growth of garnet during the formation of high‐pressure, mafic garnet‐granulite after low‐pressure mafic protoliths.     

Ultra-high-temperature metamorphism and multistage decompressional evolution of sapphirine granulites from the Palni Hill Ranges, southern India

Sapphirine granulites from a new locality in the Palni Hill Ranges, southern India, occur in a small enclave of migmatitic, highly magnesian metapelites (mg=85–72) within massive enderbitic orthogneiss. They show a variety of multiphase reaction textures that partially overprint a coarse-grained high-pressure assemblage of Bt+Opx+Ky+Grt+Pl+Qtz. The sequence of reactions as deduced from the corona and symplectite assemblages, together with petrogenetic grid considerations, records a clockwise P–T evolution with four distinct stages. (1) Equilibration of the initial high-P assemblage in deep overthickened crust (12 kbar/800–900 °C) was followed by a stage of near-isobaric heating, presumably as a consequence of input of extra heat provided by the voluminous enderbitic intrusives. During heating, kyanite was converted to sillimanite, and biotite was involved in a series of vapour-phase-absent melting reactions, which resulted in the ultra-high-temperature assemblage Opx+Crd+Kfs+Spr±Sil, Grt, Qtz, Bt, coexisting with melt (equilibration at c. 950–1000° C/11–10 kbar). (2) Subsequently, as a result of decompression of the order of 4 kbar at ultra-high temperature, a sequence of symplectite assemblages (Opx+Sil+Spr/Spr+Crd→Opx+Spr+Crd→Opx+Crd→Opx+Crd+Spl/Crd+Spl) developed at the expense of garnet, orthopyroxene and sillimanite. This stage of near-isothermal decompression implies rapid ascent of the granulites into mid-crustal levels, possibly due to extensional collapse and erosion of the overthickened crust. (3) Development of late biotite through back-reaction of melt with residual garnet indicates a stage of near-isobaric cooling to c. 875 °C at 7–8 kbar, i.e. relaxation of the rapidly ascended crust to the stable geotherm. (4) A second period of near-isothermal exhumation up to c. 6–5 kbar/850 °C is indicated by the partial breakdown of late biotite through volatile phase-absent melting reactions. Available isotope data suggest that the early part of the evolutionary history (stages 1–3) is presumably coeval with the early Proterozoic metamorphism in the extended granulite terrane of the Nilgiri, Biligirirangan and Shevaroy Hills to the north, while the exhumation of the granulites from mid-crustal levels (stage 4) occurred only during the Pan-African thermotectonic event, which led to the accretion of the Kerala Khondalite Belt to the south.     

胶北南山口古元古代高压基性麻粒岩和钙硅酸盐岩的岩石地球化学特征探讨

胶北莱西古元古代的高压基性麻粒岩和钙硅酸盐岩的基本矿物组合分别为以铁铝榴石为主的石榴石-普通辉石-铁紫苏辉石和钙铝榴石-黝帘石-葡萄石-钠长石.矿物岩石学研究表明钙硅酸盐岩是由含石榴石高压基性麻粒岩经退变质和钙质交代作用形成.南山口高压基性麻粒岩记录了麻粒岩相变质作用前、麻粒岩相变质作用、退变质和钙硅酸盐岩化共同作用以及完全钙硅酸盐岩化的四个阶段的地质作用,其矿物组合分别为Cpx+ Pl+ Qtz(M1),Grt+ Cpx+ Rt+ Qtz(M2),Cpx+Pl+ Opx+ Ilm+ Mgt+ Ep(M3)和Grs+ Zo+ Prh+ Ab+ Cal(M4).微量元素研究表明,高压基性麻粒岩中大离子亲石元素Ba、Rb、K、Rb、Th富集,而高场强元素Nb、Zr、Ti、Y亏损,具有轻稀土富集的右倾型稀土配分曲线.稀土元素和微量元素配分图解显示了岛孤拉斑玄武岩的特征.主元素、微量元素的构造判别图解进一步分析表明高压基性麻粒岩及其钙硅酸盐岩的原岩形成于大陆边缘的岛弧环境.综合高压基性麻粒岩岩石学、元素地球化学特征认为,莱西高压基性麻粒岩的原岩是拉斑玄武岩质岩石,可能是形成于孤后扩张背景下基性的侵入岩或喷出岩.岩石形成以后,在胶-辽-吉带碰撞闭合过程中,经历了麻粒岩相变质作用,又在后来的抬升过程中经历退变质和钙硅酸盐岩化作用.