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1.
Three stages of Early Proterozoic granitoid magmatism were distinguished in the southwestern margin of the Siberian craton: (1) syncollisional, including the formation of migmatites and granites in the border zone of the Tarak massif; (2) postorogenic, postcollisional, comprising numerous granitoid plutons of diverse composition; and (3) intraplate, corresponding to the development of potassic granitoids in the Podporog massif. Rocks of three petrological and geochemical types (S, I, and A) were found in the granitoid massifs. The S-type granites are characterized by the presence of aluminous minerals (garnet and cordierite), and their trace element distribution patterns and Nd isotopic parameters are similar to those of the country paragneisses and migmatites. Their formation was related to melting under varying H2O activity of aluminous and garnet—biotite gneisses at P ≥ 5 kbar and T < 850°C with a variable degree of melt separation from the residual phases. The I-type tonalites and dioritoids show low relative iron content, high concentrations of CaO and Sr, fractionated REE distribution patterns with (La/Yb)n = 11–42, and variable depletion of heavy REE. Their parental melts were derived at T ≥ 850°C and P > 10 and P < 10 kbar, respectively. According to isotopic data, their formation was related to melting of a Late Archean crustal (tonalite-diorite-gneiss) source with a contribution of juvenile material ranging from 25–55% (tonalites of the Podporog massif) to 50–70% (dioritoids of the Uda pluton). The most common A-type granitoids show high relative iron content; high concentration of high-field-strength elements, Th, and light and heavy REE; and a distinct negative Eu anomaly. Their primary melts were derived at low H2O activity and T ≥ 950°C. The Nd isotopic composition of the granitoids suggests contributions to the magma formation processes from ancient (Early and Late Archean) crustal (tonalite-diorite-gneiss) sources and a juvenile mantle material. The contribution of the latter increases from 0–35% in the granites of the Podporog and Tarak massifs to 40–50% for the rocks of the Uda and Shumikha plutons. The main factors responsible for the diversity of petrological and geochemical types of granitoids in collisional environments are the existence of various fertile sources in the section of the thickened crust of the collisional orogen, variations in magma generation conditions $(\alpha _{H_2 O} , T, and P)$ during sequential stages of granite formation, and the varying fraction of juvenile mantle material in the source region of granitoid melts.  相似文献   

2.
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.  相似文献   

3.
Partial melting of sulfide ores during prograde metamorphism could have been more prevalent than generally accepted. However, identification of such melting is difficult as sulfide melts do not form glasses and the textures generated on quenching are obliterated due to the tendency of sulfides for ready recrystallization. The polymetallic base metal sulfide deposit at Rajpura–Dariba, Rajasthan, India is a typical stratiform ore metamorphosed to the middle amphibolite facies. The peak metamorphic temperature of 600 °C should have been sufficient to initiate sulfide melting as evident from experimental studies in the ZnS–PbS–Cu2S–FeS2–S system. Further, syn-metamorphic melting of the original SEDEX ore was abetted by the high fS2 condition that prevailed as a consequence of barite dissolution. A Zn–Fe–S melt containing minor Pb, Sb and Cu but no Ag fractionated from an initial melt in the above system resulting in a residual immiscible sulfosalt-bearing PbS melt. The final metallic melts, represented by formation of dyscrasite (Ag3Sb) from the sulfosalt-bearing melt and breithauptite (NiSb) or ullmannite (NiSbS) from the sulfosalt-absent melt, were a product of independent fractional crystallization of the immiscible sulfide and PbS–sulfosalt melts.  相似文献   

4.
Melt inclusions and aqueous fluid inclusions in quartz phenocrysts from host felsic volcanics, as well as fluid inclusions in minerals of ores and wall rocks were studied at the Cu-Zn massive sulfide deposits in the Verkhneural’sk ore district, the South Urals. The high-temperature (850–1210°C) magmatic melts of volcanic rocks are normal in alkalinity and correspond to rhyolites of the tholeiitic series. The groups of predominant K-Na-type (K2O/Na2O = 0.3–1.0), less abundant Na-type (K2O/Na2O = 0.15–0.3), and K-type (K2O/Na2O = 1.9–9.3) rhyolites are distinguished. The average concentrations (wt %) of volatile components in the melts are as follows: 2.9 H2O (up to 6.5), 0.13 Cl (up to 0.28), and 0.09 F (up to 0.42). When quartz was crystallizing, the melt was heterogeneous, contained magnetite crystals and sulfide globules (pyrrhotite, pentlandite, chalcopyrite, bornite). High-density aqueous fluid inclusions, which were identified for the first time in quartz phenocrysts from felsic volcanics of the South Urals, provide evidence for real participation of magmatic water in hydrothermal ore formation. The fluids were homogenized at 124–245°C in the liquid phase; the salinity of the aqueous solution is 1.2–6.2 wt % NaCl equiv. The calculated fluid pressure is very high: 7.0–8.7 kbar at 850°C and 5.1–6.8 kbar at 700°C. The LA-ICP-MS analysis of melt and aqueous fluid inclusions in quartz phenocrysts shows a high saturation of primary magmatic fluid and melt with metals. This indicates ore potential of island-arc volcanic complexes spatially associated with massive sulfide deposits. The systematic study of fluid inclusions in minerals of ores and wall rocks at five massive sulfide deposits of the Verkhneural’sk district furnished evidence that ore-forming fluids had temperature of 375–115°C, pressure up to 1.0–0.5 kbar, chloride composition, and salinity of 0.8–11.2 (occasionally up to 22.8) wt % NaCl equiv. The H and O isotopic compositions of sericite from host metasomatic rocks suggest a substantial contribution of seawater to the composition of mineral-forming fluids. The role of magmatic water increases in the central zones of the feeding conduit and with depth. The dual nature of fluids with the prevalence of their magmatic source is supported by S, C, O, and Sr isotopic compositions. The TC parameters of the formation of massive sulfide deposits are consistent with the data on fluid inclusions from contemporary sulfide mounds on the oceanic bottom.  相似文献   

5.
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6.
The El Arenal metagabbros preserve coronitic shells of orthopyroxene ± Fe‐oxide around olivine, as well as three different types of symplectite consisting of amphibole + spinel, clinopyroxene + spinel and, more rarely, orthopyroxene + spinel. The textural features of the metagabbros can be explained by the breakdown of the olivine + plagioclase pair, producing orthopyroxene coronas and clinopyroxene + spinel symplectites, followed by the formation of amphibole + spinel symplectites, reflecting a decrease in temperature and, possibly, an increase in water activity with respect to the previous stage. The metagabbros underwent a complex P–T history consisting of an igneous stage followed by cooling in granulite, amphibolite and greenschist facies conditions. Although the P–T conditions of emplacement of the igneous protolith are still doubtful, the magmatic assemblage suggests that igneous crystallization occurred at a pressure lower than 6 kbar and at 900–1100 °C. Granulitic P–T conditions have been estimated at about 900 °C and 7–8 kbar combining conventional thermobarometry and pseudosection analysis. Pseudosection calculation has also shown that the formation of the amphibole + spinel symplectite could have been favoured by an increase in water activity during the amphibolite stage, as the temperature of formation of this symplectite strongly depends on aH2O (<740 °C for aH2O = 0.5; <790 °C for aH2O = 1). Furthermore, but not pervasive, re‐equilibration under greenschist facies P–T conditions is documented by retrograde epidote and chlorite. The resulting counterclockwise P–T path consists of progressive, nearly isobaric cooling from the igneous stage down to the granulite, amphibolite and greenschist stage.  相似文献   

7.
In this paper, we show that the crystallization of miarolitic pegmatites at K?nigshain started at about 700°C, in melts containing up to 30 mass% water. Such high water concentration at low pressures (1–3 kbar) is only possible if the melts are peralkaline. Such peralkaline melts are highly corrosive, and reacted with the wall rock—here the granite host—forming the graphic granite zone, in part via a magmatic–metasomatic reaction. With cooling, the water concentration in some melt fractions increased up to 50 mass% H2O. The melt-dominated system ends below 600°C and passes into a fluid-dominated system, the beginning of which is characterized by strong pressure fluctuations, caused by the change of OH and CO3 2− in the melt, to molecular water and CO2. We note two generations of smoky quartz, one crystallized above the β–α-transition of quartz (≈573°C), and one below, both of which contain melt inclusions. This indicates that some melt fraction remains during at least the higher-temperature portion of the growth of minerals into the miarolitic cavity, contradicting the view that minerals growing into a pegmatite chamber only do so from aqueous fluids. We show that the K?nigshain miarolitic pegmatites are part of the broad spectrum of pegmatite types, and the processes active at K?nigshain are representative of processes found in most granitic pegmatites, and are thus instructive in the understanding of pegmatite formation in general, and constraining the composition and characteristics of pegmatite-forming melts. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

8.
Major elements, highly siderophile elements (HSE) and Re-Os isotope ratios were analysed in situ on individual sulfide grains in spinel peridotite xenoliths hosted by Miocene intraplate basalts from the Penghu Islands, Taiwan. The xenoliths represent texturally and compositionally different mantle domains, and the geochemical characteristics of the sulfides show changes in HSE distribution and Re-Os isotope systematics, produced as their host rocks were metasomatised by percolating fluids/melts. In prophyroclastic and partly metasomatised peridotites from the Kueipi (KP) locality, the sulfides have subchondritic to superchondritic 187Re/188Os and 187Os/188Os ratios. Many of these sulfides reflect fluid/melt interaction with residual MSS and/or crystallization of fractionated sulfide melts, which produced high contents of Cu and PPGEs and high Re/Os; inferred melt/rock ratios are low. In contrast, sulfides in equigranular and extensively metasomatised peridotites from the Tungchiyu (TCY) locality are mainly more sulfur-rich Ni-(Co)-rich MSS, with subchondritic to chondritic 187Os/188Os and subchondritic 187Re/188Os. These sulfides are interpreted as products of interaction between pre-existing MSS and percolating silicate melts. Melt/rock ratios were high and the percolating melt was less differentiated than the melt that percolated the KP peridotites. Sulfides in a TCY pyroxenite are mainly MSS; they have the lowest HSE contents, subchondritic to superchondritic 187Os/188Os and subchondritic 187Re/188Os, and may have precipitated from sulfide melts that segregated from basaltic melts under S-saturated conditions. In most sulfides melt percolation appears to have induced fractionation among the HSEs and disturbed Re-Os isotope compositions. Despite the metasomatic effects, rare residual MSS, sulfides that from crystallised sulfide melts and sulfides modified by addition of Re (with no evidence for Os addition) can still provide useful chronological information. Such sulfides yield TRD age peaks of 1.9, 1.7-1.6, 1.4-1.3 and 0.9-0.8 Ga, which may record the timing of melt extraction and/or metasomatic events in the mantle. These periods are contemporaneous with the major crustal events recorded by U-Pb dates and Nd and Hf model ages in the overlying crust. This close correspondence indicates that the sulfide TRD ages reflect the timing of lithosphere-scale tectonothermal events (such as melting and metasomatism) that affected both the lithospheric mantle and the overlying crust. The sulfide TRD ages, taken together with the crustal data, suggest that most of the Cathaysia block had formed at least by Paleo-Proterozoic time, and that some domains are Archean in age.  相似文献   

9.
Mantle xenoliths (lherzolites, clinopyroxene dunites, wehrlites, and clinopyroxenites) in the Early Cretaceous volcanic rocks of Makhtesh Ramon (alkali olivine basalts, basanites, and nephelinites) represent metasomatized mantle, which served as a source of basaltic melts. The xenoliths bear signs of partial melting and previous metasomatic transformations. The latter include the replacement of orthopyroxene by clinopyroxene in the lherzolites and, respectively, the wide development of wehrlites and olivine clinopyoroxenites. Metasomatic alteration of the peridotites is accompanied by a sharp decrease in Mg, Cr, and Ni, and increase of Ti, Al, Ca contents and 3+Fe/2+Fe ratio, as well as the growth of trace V, Sc, Zr, Nb, and Y contents. The compositional features of the rocks such as the growth of 3+Fe/2+Fe and the wide development of Ti-magnetite in combination with the complete absence of sulfides indicate the high oxygen fugacity during metasomatism and the low sulfur concentration, which is a distinctive signature of fluid mode during formation of the Makhtesh Ramon alkali basaltic magma. Partial melting of peridotites and clinopyroxenites is accompanied by the formation of basanite or alkali basaltic melt. Clino- and orthopyroxenes are subjected to melting. The crystallization products of melt preserved in the mantle rock are localized in the interstices and consist mainly of fine-grained clinopyroxene, which together with Ti-magnetite, ilmenite, amphibole, rhenite, feldspar, and nepheline, is cemented by glass corresponding to quartz–orthopyroxene, olivine–orthopyroxene, quartz–feldspar, or nepheline–feldspar mixtures of the corresponding normative minerals. The mineral assemblages of xenoliths correspond to high temperatures. The high-Al and high-Ti clinopyroxene, calcium olivine, feldspar, and feldspathoids, amphibole, Ti-magnetite, and ilmenite are formed at 900–1000°. The study of melt and fluid inclusions in minerals from xenoliths indicate liquidus temperatures of 1200–1250°C, solidus temperatures of 1000–1100°C, and pressure of 5.9–9.5 kbar. Based on the amphibole–plagioclase barometer, amphibole and coexisting plagioclase were crystallized in clinopyroxenites at 6.5–7.0 kbar.  相似文献   

10.
In this study, we investigate the metamorphic history of the Assynt and Gruinard blocks of the Archean Lewisian Complex, northwest Scotland, which are considered by some to represent discrete crustal terranes. For samples of mafic and intermediate rocks, phase diagrams were constructed in the Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–O2 (NCKFMASHTO) system using whole‐rock compositions. Our results indicate that all samples equilibrated at similar peak metamorphic conditions of ~8–10 kbar and ~900–1,000°C, consistent with field evidence for in situ partial melting and the classic interpretation of the central region of the Lewisian Complex as representing a single crustal block. Melt‐reintegration modelling was employed in order to estimate probable protolith compositions. Phase equilibria calculated for these modelled undepleted precursors match well with those determined for a subsolidus amphibolite from Gairloch in the southern region of the Lewisian Complex. Both subsolidus lithologies exhibit similar phase relations and potential melt fertility, with both expected to produce orthopyroxene‐bearing hornblende granulites, with or without garnet, at the conditions inferred for the Badcallian metamorphic peak. For fully hydrated protoliths, prograde melting is predicted to first occur at ~620°C and ~9.5 kbar, with up to 45% partial melt predicted to form at peak conditions in a closed‐system environment. Partial melts calculated for both compositions between 610 and 1,050°C are mostly trondhjemitic. Although the melt‐reintegrated granulite is predicted to produce more potassic (granitic) melts at ~700–900°C, the modelled melts are consistent with the measured compositions of felsic sheets from the central region Lewisian Complex.  相似文献   

11.
Dehydration-melting of Biotite Gneiss and Quartz Amphibolite from 3 to 15 kbar   总被引：80，自引：20，他引：60  
We performed vapor-absent melting and crystallization experimentson two bulk compositions that model metamorphic rocks containinga single hydrous phase: a biotite gneiss [37% bio (mg-number55), 34% qtz, 27% plg (An38), 2% ilm] and a quartz amphibolite[54% hbl (mg-number 60), 24% qtz, 20% plg (An38), 2% ilm]. Experimentswere performed at 3 and 5 kbar in internally heated pressurevessels (IHPV), and at 7, 10, 125 and 15 kbar in piston cylinderapparatus (PC), from the vapor-absent solidi to (at least) thetemperature at which the hydrous mineral disappeared. Dehydration-meltingbegins at similar temperatures in both bulk compositions, rangingfrom T850C at P = 3 kbar T930C at P = 15 kbar. The hydrousmineral disappears 50C above the solidus in both systems, exceptin IHPV experiments at f(O2) above Ni–NiO, in which biotitestability extends up to atleast 80C above the solidus. At theT at which the hydrous minerals disappear the biotite gneissproduces 2–3 times more melt than the quartz amphibolite(50–60 wt% vs 20–30 wt%). In both systems, variationsin melt productivity with P are controlled by three competingfactors: (1) the positive d P/dT slopes of the solidi, (2) decreasingH2O activity with increasing P at constant H2O content, and(3) Na2O activity, which increases with P concomitantly withbreakdown of plagioclase. Melt productivities at T = 920–950Care maximized at intermediate pressures (7 kbar). The biotitegneiss produces strongly peraluminous granitic melts (SiO2>70wt%) and residual assemblages of quartz norite (P>125 kbar)or garnet pyroxenite (P>125 kbar). The quartz amphiboliteproduces strongly peraluminous granodioritic melts (SiO2>70wt%) that coexist with clinopyroxene + orthopyroxene + plagioclase+ quartz at P>10 kbar)garnet. The results of coupled meltingand crystallization experiments on the quartz amphibolite suggestthat strongly peraluminous granitoid rocks (e.g. cordierite-bearingand two-mica granites) can be derived from melting of Al-poorprotoliths. KEY WORDS: dehydration-melting; biotite gneiss; amphibolite; felsic magmas *Corresponding author  相似文献   

12.
The P–T evolution of amphibolite facies gneisses and associated supracrustal rocks exposed along the northern margin of the Paleo to MesoArchean Barberton greenstone belt, South Africa, has been reconstructed via detailed structural analysis combined with calculated K(Mn)FMASH pseudosections of aluminous felsic schists. The granitoid‐greenstone contact is characterized by a contact‐parallel high‐strain zone that separates the generally low‐grade, greenschist facies greenstone belt from mid‐crustal basement gneisses. The supracrustal rocks in the hangingwall of this contact are metamorphosed to upper greenschist facies conditions. Supracrustal rocks and granitoid gneisses in the footwall of this contact are metamorphosed to sillimanite grade conditions (600–700 °C and 5 ± 1 kbar), corresponding to elevated geothermal gradients of ～30–40 °C km?1. The most likely setting for these conditions was a mid‐ or lower crust that was invaded and advectively heated by syntectonic granitoids at c. 3230 Ma. Combined structural and petrological data indicate the burial of the rocks to mid‐crustal levels, followed by crustal exhumation related to the late‐ to post‐collisional extension of the granitoid‐greenstone terrane during one progressive deformation event. Exhumation and decompression commenced under amphibolite facies conditions, as indicated by the synkinematic growth of peak metamorphic minerals during extensional shearing. Derived P–T paths indicate near‐isothermal decompression to conditions of ～500–650 °C and 1–3 kbar, followed by near‐isobaric cooling to temperatures below ～500 °C. In metabasic rock types, this retrograde P–T evolution resulted in the formation of coronitic Ep‐Qtz and Act‐Qtz symplectites that are interpreted to have replaced peak metamorphic plagioclase and clinopyroxene. The last stages of exhumation are characterized by solid‐state doming of the footwall gneisses and strain localization in contact‐parallel greenschist‐facies mylonites that overprint the decompressed basement rocks.  相似文献   

13.
Of great importance in the problem of redox evolution of mantle rocks is the reconstruction of scenarios of alteration of Fe0- or Fe3C-bearing rocks by oxidizing mantle metasomatic agents and the evaluation of stability of these phases under the influence of fluids and melts of different compositions. Original results of high-temperature high-pressure experiments (P = 6.3 GPa, T = 1300–1500°С) in the carbide–oxide–carbonate systems (Fe3C–SiO2–(Mg,Ca)CO3 and Fe3C–SiO2–Al2O3–(Mg,Ca)CO3) are reported. Conditions of formation of mantle silicates with metallic or metal–carbon melt inclusions are determined and their stability in the presence of CO2-fluid representing the potential mantle oxidizing metasomatic agent are estimated. It is established that garnet or orthopyroxene and CO2-fluid are formed in the carbide–oxide–carbonate system through decarbonation, with subsequent redox interaction between CO2 and iron carbide. This results in the formation of assemblage of Fe-rich silicates and graphite. Garnet and orthopyroxene contain inclusions of a Fe–C melt, as well as graphite, fayalite, and ferrosilite. It is experimentally demonstrated that the presence of CO2-fluid in interstices does not affect on the preservation of metallic inclusions, as well as graphite inclusions in silicates. Selective capture of Fe–C melt inclusions by mantle silicates is one of the potential scenarios for the conservation of metallic iron in mantle domains altered by mantle oxidizing metasomatic agents.  相似文献   

14.
Dehydration melting of tonalites. Part II. Composition of melts and solids   总被引：6，自引：0，他引：6  
 Dehydration melting of tonalitic compositions (phlogopite or biotite-plagioclase-quartz assemblages) is investigated within a temperature range of 700–1000°C and pressure range of 2–15 kbar. The solid reaction products in the case of the phlogopite-plagioclase(An45)-quartz starting material are enstatite, clinopyroxene and potassium feldspar, with amphiboles occurring occasionally. At 12 kbar, zoisite is observed below 800°C, and garnet at 900°C. The reaction products of dehydration melting of the biotite (Ann50)-plagioclase (An45)-quartz assemblage are melt, orthopyroxene, clinopyroxene, amphibole and potassium feldspar. At pressures > 8 kbar and temperatures below 800°C, epidote is also formed. Almandine-rich garnet appears above 10 kbar at temperatures ≥ 750°C. The composition of melts is granitic to granodioritic, hence showing the importance of dehydration melting of tonalites for the formation of granitic melts and granulitic restites at pressure-temperature conditions within the continental crust. The melt compositions plot close to the cotectic line dividing the liquidus surfaces between quartz and potassium feldspar in the haplogranite system at 5 kbar and a H 2O = 1. The composition of the melts changes with the composition of the starting material, temperature and pressure. With increasing temperature, the melt becomes enriched in Al2O3 and FeO+MgO. Potash in the melt is highest just when biotite disappears. The amount of CaO decreases up to 900°C at 5 kbar whereas at higher temperatures it increases as amphibole, clinopyroxene and more An-component dissolve in the melt. The Na2O content of the melt increases slightly with increase in temperature. The composition of the melt at temperatures > 900°C approaches that of the starting assemblage. The melt fraction varies with composition and proportion of hydrous phases in the starting composition as well as temperature and pressure. With increasing modal biotite from 20 to 30 wt%, the melt proportion increases from 19.8 to 22.3 vol.% (850°C and 5 kbar). With increasing temperature from 800 to 950°C (at 5 kbar), the increase in melt fraction is from 11 to 25.8 vol.%. The effect of pressure on the melt fraction is observed to be relatively small and the melt proportion in the same assemblage decreases at 850°C from 19.8 vol.% at 5 kbar to 15.3 vol.% at 15 kbar. Selected experiments were reversed at 2 and 5 kbar to demonstrate that near equilibrium compositions were obtained in runs of longer duration. Received: 27 December 1995 / Accepted: 7 May 1996  相似文献   

15.
Plagioclase-bearing garnet-omphacite (Grt-Omp) eclogites and garnet-augite eclogite-like (Grt-Aug) schists from the amphibolite and gneiss beds of the Belomorian Mobile Belt have been studied. They are spread over a large area. In most of the studied objects, these rocks have preserved primary concordant relations with the host amphibolite and gneiss strata; they are not disturbed by late tectonic processes and are not genetically related to tectonic-melange zones. Their protoliths were amphibolite lenses in gneisses or large mafic zones composed of amphibolites. The Grt-Omp eclogites formed in the low-pressure field of the eclogite facies (P = 12.5-13.0 kbar, T = 600-630 °C), and the eclogite-like Grt-Aug rocks, at the boundary between the amphibolite and eclogite facies (P = 9.6-11.1 kbar, T = 630-700 °C), under the intense impact of metamorphic fluid on the amphibolites. The compositional evolution of the rock-forming minerals during the formation of Grt-Omp eclogites and eclogite-like Grt-Aug rocks followed the same scheme. The petrographic diversity of apoamphibolite rocks (Grt-Omp eclogites and Grt-Aug schists) might be due to the difference both in the bulk composition of the metabasic protolith and in the ratios of CaO and Na2O activities in the metamorphic fluid. The relatively low content of CaO leads to the formation of Grt-Omp paragenesis in eclogites. Higher CaO contents give rise to eclogite-like Grt-Aug rocks containing jadeite-poor clinopyroxene.  相似文献   

16.
This paper investigates the age, P–T conditions and kinematics of Karakorum Fault (KF) zone rocks in the NW part of the Himalaya–Karakorum belt. Granulite to greenschist facies assemblages were developed within the KF zone during strike-slip shearing. The granulites were formed at high temperature (800 °C, 5.5 kbar), were subsequently retromorphosed into the amphibolite facies (700–750 °C, 4–5 kbar) and the greenschist facies (350–400 °C, 3–4 kbar). The Tangtse granite emplaced syn-kinematically at the contact between a LT and the HT granulite facies. Intrusion occurred during the juxtaposition of the two units under amphibolite conditions. Microstructures observed within the Tangtse granite exhibit a syn-magmatic dextral S–C fabric. Compiled U–Pb and Ar–Ar data show that in the central KF segment, granulite facies metamorphism occurred at a minimum age of 32 Ma, subsequent amphibolite facies metamorphism at 20–18 Ma. Further shearing under amphibolite facies (650–500 °C) was recorded at 13.6 ± 0.9 Ma, and greenschist-facies mica growth at 11 Ma. These data give further constrains to the age of initiation and depth of the Karakorum Fault. The granulite-facies conditions suggest that the KF, accommodating the lateral extrusion of Tibet, could be at least a crustal or even a Lithosphere-scale shear zone comparable to other peri-Himalayan faults.  相似文献   

17.
《International Geology Review》2012,54(13):1715-1734
This study examines the geochemistry of major and trace elements of abyssal peridotites from the Southwest Indian Ridge (SWIR) (53° E amagmatic segment), to determine the influence of mafic melts on mantle peridotites during melt extraction. The results show a great geochemical variability in the ~90 km-long ridge segment, with a degree of mantle melting ranging from 4% to 24%. An ancient melting event may explain the presence of highly depleted peridotites at the ultraslow-spreading ridge. The 53° E segment peridotites show enrichment of light rare earth elements (LREEs) (average LaN/SmN = 1.87) and significant positive anomaly of U and Pb normalized to primitive mantle (PM). The positive correlations between LREEs (La, Ce, Pr, Nd) and high field strength elements (HFSEs; e.g. Nb and Zr) suggest that the enrichment of LREEs is caused by melt refertilization, which is also supported by prevalent magmatic microstructures in the peridotites. The melt refertilization model shows that the addition of 0.02–2.7% basaltic melts to peridotites can be responsible for the LREE enrichment. We suggest that the positive anomaly of U is probably attributed to fluid alteration whereas the enrichment of Pb is probably attributed to both melt refertilization and fluid alteration. Melt refertilization in the 53° E segment peridotites may be a result of melt–rock reaction and crystallization of melts trapped in peridotites. These processes may be enhanced by increased melt permeability in the mantle owing to the refractory peridotites produced by ancient melting and the decreasing efficiency of melt extraction in the cold and thick lithosphere at the 53° E ridge segment. The presence of melt refertilization implies that melt extraction is incomplete in the ridge mantle, which may be one of the reasons for the extremely thin and irregular variation of the crustal thickness at ultraslow-spreading ridges.  相似文献   

18.
Garnet–spinel lherzolites from Antarctica and peridotites from Mongolia were fluid saturated, which is indicated by the presence of fluid inclusions in their minerals. Flows of reactive fluids caused extensive metasomatic alteration of mantle materials. The cryometric and Raman spectroscopic investigation of the Antarctic xenoliths showed that their fluid was a complex mixture of CO2, N2, H2S, and H2O with a density of up to 1.23 g/cm3. The entrapment of fluids was accompanied by the formation of clusters of numerous sulfide inclusions. The compositions of these inclusions correspond to a Ni-rich sulfide melt and a monosulfide solid solution. The partition coefficient of Ni between them (DNi mss/melt) ranges from 0.99 to 3.23, which suggests that the two-phase sulfide assemblages in the partly decrepitated inclusions equilibrated at 920–1060°C. In order to refine the initial P-T conditions of the development of the Antarctic peridotites, the results of our investigation were evaluated in the light of experimental data on (1) the stability field of the two-phase assemblage mss + sulfide melt, (2) the solidus of peridotite + 0.9CO2 + 0.1 H2O, and (3) isochores of 0.8CO2 + 0.2N2 fluid. The obtained parameters are close to 1270–1280°C and 2.2 GPa and lie near the Sp–Gar boundary. The temperature of the existence of sulfide melt at a pressure of 2.2 GPa must be near 1300°C and corresponds to the boundary between the occurrence of carbon as CO2 fluid and carbonate (carbonate melt).  相似文献   

19.
We document the presence of dolomite ± apatite in orogenic peridotites from the Ulten Zone (UZ, Italian Alps), the remnants of a Variscan mantle wedge tectonically coupled with eclogitized continental crust. These dolomite peridotites are associated with dominant carbonate-free amphibole peridotites, which formed in response to infiltration of aqueous subduction fluids lost by the associated crustal rocks during high-pressure (HP) metamorphism and retrogression. Dolomite-free and dolomite-bearing peridotites share the same metamorphic evolution, from garnet- (HP) to spinel-facies (low-pressure, LP) conditions. Dolomite and the texturally coexisting phases display equilibrium redistribution of rare earth elements and of incompatible trace elements during HP and LP metamorphism; clinopyroxene and amphiboles from carbonate-free and carbonate-bearing peridotites have quite similar compositions. These features indicate that the UZ mantle rocks equilibrated with the same metasomatic agents: aqueous CO2-bearing fluids enriched in incompatible elements released by the crust. The P–T crystallization conditions of the dolomite peridotites (outside the field of carbonatite melt + amphibole peridotite coexistence), a lack of textures indicating quench of carbonic melts, a lack of increase in modal clinopyroxene by reaction with such melts and the observed amphibole increase at the expense of clinopyroxene, all suggest that dolomite formation was assisted by aqueous CO2-bearing fluids. A comparison of the trace element compositions of carbonates and amphiboles from the UZ peridotites and from peridotites metasomatized by carbonatite and/or carbon-bearing silicate melts does not help to unambiguously discriminate between the different agents (fluids or melts). The few observed differences (lower trace element contents in the fluid-related dolomite) may ultimately depend on the solute content of the metasomatic agent (CO2-bearing fluid versus carbonatite melt). This study provides strong evidence that C–O–H subduction fluids can produce ‘carbonatite-like’ assemblages in mantle rocks, thus being effective C carriers from the slab to the mantle wedge at relatively low P–T. If transported beyond the carbonate and amphibole solidus by further subduction, dolomite-bearing garnet + amphibole peridotites like the ones from Ulten can become sources of carbonatite and/or C-bearing silicate melts in the mantle wedge. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users. In memory of Lauro Morten 1941–2006.  相似文献   

20.
Abstract Eclogites are distributed for more than 500 km along a major tectonic boundary between the Sino-Korean and Yangtze cratons in central and eastern China. These eclogites usually have high-P assemblages including omphacite + kyanite and/or coesite (or its pseudomorph), and form a high-P eclogite terrane. They occur as isolated lenses or blocks 10 cm to 300 m long in gneisses (Type I), serpentinized garnet peridotites (Type II) and marbles (Type III). Type I eclogites were formed by prograde metamorphism, and their primary metamorphic mineral assemblage consists mainly of garnet [pyrope (Prp) = 15–40 mol%], omphacite [jadeite (Jd) = 34–64 mol%], pargasitic amphibole, kyanite, phengitic muscovite, zoisite, an SiO2 phase, apatite, rutile and zircon. Type II eclogites characteristically contain no SiO2 phase, and are divided into prograde eclogites and mantle-derived eclogites. The prograde eclogites of Type II are petrographically similar to Type I eclogites. The mantle-derived eclogites have high MgO/(FeO + Fe2O3) and Cr2O3 compositions in bulk rock and minerals, and consist mainly of pyrope-rich garnet (Prp = 48–60 mol%), sodic augite (Jd = 10–27 mol%) and rutile. Type III eclogites have an unusual mineral assemblage of grossular-rich (Grs = 57 mol%) garnet + omphacite (Jd = 30–34 mol%) + pargasite + rutile. Pargasitic and taramitic amphiboles, calcic plagioclase (An68), epidote, zoisite, K-feldspar and paragonite occur as inclusions in garnet and omphacite in the prograde eclogites. This suggests that the prograde eclogites were formed by recrystallization of epidote amphibolite and/or amphibolite facies rocks with near-isothermal compression reflecting crustal thickening during continent–continent collision of late Proterozoic age. Equilibrium conditions of the prograde eclogites range from P > 26 kbar and T= 500–750°C in the western part to P > 28 kbar and T= 810–880°C in the eastern part of the high-P eclogite terrane. The prograde eclogites in the eastern part are considered to have been derived from a deeper position than those in the western part. Subsequent reactions, manifested by (1) narrow rims of sodic plagioclase or paragonite on kyanite and (2) symplectites between omphacite and quartz are interpreted as an effect of near-isothermal decompression during the retrograde stage. The conditions at which symplectites re-equilibrated tend to increase from west (P < 10 kbar and T < 580°C) to east (P > 9 kbar and T > 680°C). Equilibrium temperatures of Type II mantle-derived eclogites and Type III eclogite are 730–750°C and 680°C, respectively.  相似文献   

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