Conditions and timing of high-pressure Variscan metamorphism in the South Carpathians, Romania   总被引：2，自引：0，他引：2  

Gordon Medaris Jr.  Mihai Ducea  Ed Ghent  Viorica Iancu 《Lithos》2003,70(3-4):141-161

High-pressure (HP) metamorphic rocks, including garnet peridotite, eclogite, HP granulite, and HP amphibolite, are important constituents of several tectonostratigraphic units in the pre-Alpine nappe stack of the Getic–Supragetic (GS) basement in the South Carpathians. A Variscan age for HP metamorphism is firmly established by Sm–Nd mineral–whole-rock isochrons for garnet amphibolite, 358±10 Ma, two samples of eclogite, 341±8 and 344±7 Ma, and garnet peridotite, 316±4 Ma.

A prograde history for many HP metamorphic rocks is documented by the presence of lower pressure mineral inclusions and compositional zoning in garnet. Application of commonly accepted thermobarometers to eclogite (grt+cpx±ky±phn±pg±zo) yields a range in “peak” pressures and temperatures of 10.8–22.3 kbar and 545–745 °C, depending on tectonostratigraphic unit and locality. Zoisite equilibria indicate that activity of H₂O in some samples was substantially reduced, ca. 0.1–0.4. HP granulite (grt+cpx+hb+pl) and HP amphibolite (grt+hbl+pl) may have formed by retrogression of eclogites during high-temperature decompression. Two types of garnet peridotite have been recognized, one forming from spinel peridotite at ca. 1150–1300 °C, 25.8–29.0 kbar, and another from plagioclase peridotite at 560 °C, 16.1 kbar.

The Variscan evolution of the pre-Mesozoic basement in the South Carpathians is similar to that in other segments of the European Variscides, including widespread HP metamorphism, in which P–T–t characteristics are specific to individual tectonostratigraphic units, the presence of diverse types of garnet peridotite, diachronous subduction and accretion, nappe assembly in pre-Westphalian time due to collision of Laurussia, Gondwana, and amalgamated terranes, and finally, rapid exhumation, cooling, and deposition of eroded debris in Westphalian to Permian sedimentary basins.  相似文献   

Status report on stability of K-rich phases at mantle conditions   总被引：1，自引：0，他引：1  

George E. Harlow  Rondi Davies 《Lithos》2004,77(1-4):647-653

Experimental research on K-rich phases and observations from diamond inclusions, UHP metamorphic rocks, and xenoliths provide insights about the hosts for potassium at mantle conditions. K-rich clinopyroxene (Kcpx–KM³⁺Si₂O₆) can be an important component in clinopyroxenes at P>4 GPa, dependent upon coexisting K-bearing phases (solid or liquid) but not, apparently, upon temperature. Maximum Kcpx content can reach 25 mol%, with 17 mol% the highest reported in nature. Partitioning ^(K)D_(cpx/liquid) above 7 GPa=0.1–0.2 require ultrapotassic liquids to form highly potassic cpx or critical solid reactions, e.g., between Kspar and Di. Phlogopite can be stable to about 8 GPa at 1250 °C where either amphibole or liquid forms. When fluorine is present, it generally increases in Phl upon increasing P (and probably T) to about 6 GPa, but reactions forming amphibole and/or KMgF₃ limit F content between 6 and 8 GPa. The perovskite KMgF₃ is stable up to 10 GPa and 1400 °C as subsolidus breakdown products of phlogopite upon increasing P. ^(M4)K-substituted potassic richterite (ideally K(KCa)Mg₅Si₈O₂₂(OH,F)₂) is produced in K-rich peridotites above 6 GPa and in Di+Phl from 6 to 13 GPa. K content of amphibole is positively correlated with P; Al and F content decrease with P. In the system 1Kspar+1H₂O K-cymrite (hydrous hexasanidine–KAlSi₃O₈·nH₂O–Kcym) is stable from 2.5 GPa at 400 to 1200 °C and 9 GPa; Kcym can be a supersolidus phase. Formation of Kcym is sensitive to water content, not forming within experiments with H₂O2O>Kspar. Phase X, a potassium di-magnesium acid disilicate ((K_1−x−n)₂(Mg_1−nM_n³⁺)₂Si₂O₇H_2x), forms in mafic compositions at T=1150–1400 °C and P=9–17 GPa and is a potential host for K and H₂O at mantle conditions with a low-T geotherm or in subducting slabs. The composition of phase-X is not fixed but actually represents a solid solution in the stoichiometries □₂Mg₂Si₂O₇H₂–(K□)Mg₂Si₂O₇H–K₂Mg₂Si₂O₇ (□=vacancy), apparently stable only near the central composition. K-hollandite, KAlSi₃O₈, is possibly the most important K-rich phase at very high pressure, as it appears to be stable to conditions near the core–mantle boundary, 95 GPa and 2300 °C. Other K-rich phases are considered.  相似文献   

Effect of Fe on garnet–melt trace element partitioning: experiments in FCMAS and quantification of crystal-chemical controls in natural systems     

Wim van Westrenen  Jonathan D. Blundy  Bernard J. Wood 《Lithos》2000,53(3-4):189-201

Garnet–melt trace element partitioning experiments were performed in the system FeO–CaO–MgO–Al₂O₃–SiO₂ (FCMAS) at 3 GPa and 1540°C, aimed specifically at studying the effect of garnet Fe²⁺ content on partition coefficients (D^Grt/Melt). D^Grt/Melt, measured by SIMS, for trivalent elements entering the garnet X-site show a small but significant dependence on garnet almandine content. This dependence is rationalised using the lattice strain model of Blundy and Wood [Blundy, J.D., Wood, B.J., 1994. Prediction of crystal–melt partition coefficients from elastic moduli. Nature 372, 452–454], which describes partitioning of an element i with radius r_i and valency Z in terms of three parameters: the effective radius of the site r₀(Z), the strain-free partition coefficient D₀(Z) for a cation with radius r₀(Z), and the apparent compressibility of the garnet X-site given by its Young's modulus E_X(Z). Combination of these results with data in Fe-free systems [Van Westrenen, W., Blundy, J.D., Wood, B.J., 1999. Crystal-chemical controls on trace element partitioning between garnet and anhydrous silicate melt. Am. Mineral. 84, 838–847] and crystal structure data for spessartine, andradite, and uvarovite, leads to the following equations for r₀(3+) and E_X(3+) as a function of garnet composition (X) and pressure (P):Accuracy of these equations is shown by application to the existing garnet–melt partitioning database, covering a wide range of P and T conditions (1.8 GPa<P<5.0 GPa; 975°C<T<1640°C). D^Grt/Melt for all 3+ elements entering the X-site (REE, Sc and Y) are predicted to within 10–40% at given P, T, and X, when D^Grt/Melt for just one of these elements is known. In the absence of such knowledge, relative element fractionation (e.g. D_Sm^Grt/Melt/D_Nd^Grt/Melt) can be predicted. As an example, we predict that during partial melting of garnet peridotite, group A eclogite, and garnet pyroxenite, r₀(3+) for garnets ranges from 0.939±0.005 to 0.953±0.009 Å. These values are consistently smaller than the ionic radius of the heaviest REE, Lu. The above equations quantify the crystal-chemical controls on garnet–melt partitioning for the REE, Y and Sc. As such, they represent a major advance en route to predicting D^Grt/Melt for these elements as a function of P, T and X.  相似文献   

Experimental calibration of sapphirine–spinel Fe–Mg exchange thermometer: Implication for constraints on P–T condition of Howard Hills, Napier Complex, East Antarctica     

Kei Sato  Tomoharu Miyamoto  Toshisuke Kawasaki 《Gondwana Research》2006,9(4):398-408

The Fe²⁺–Mg distribution coefficients between sapphirine and spinel:were experimentally determined at pressures of 9–13 kbar and temperatures of 950–1150 °C using a natural ultrahigh-temperature (UHT) granulite with paragenesis of these minerals from the Napier Complex in East Antarctica [X_Mg = Mg / (Fe + Mg); X_Fe = Fe / (Fe + Mg)]. A new sapphirine–spinel geothermometer has been obtained as:

We applied the exchange thermometer to UHT or high-grade metamorphic rocks that were reported from various complexes in the world. If the K_D values of 2.63–4.34 obtained from low-Cr mineral pairs such as X_Cr^Spr < 0.016 and X_Cr^Spl < 0.047 were substituted into the equation, their temperature conditions would be estimated as 806–1050 °C at 11 kbar. The X_Cr means Cr / (Al + Cr(+ Fe³⁺)). These temperatures are reasonable retrograde or near peak metamorphic condition.  相似文献   

Titanian clinohumite–garnet–pyroxene rock from the Su-Lu UHP metamorphic terrane, China: chemical evolution and tectonic implications     

Jian-Jun Yang   《Lithos》2003,70(3-4):359-379

A garnet–pyroxene rock containing abundant Ti-clinohumite (ca. 40 vol.%) occurs along with eclogites as small blocks in quartzo-feldsparthic gneiss in the southern end of the Chinese Su-Lu ultrahigh-pressure (UHP) metamorphic terrane. It consists of three aggregates: (1) Ti-clinohumite-dominated aggregate with interstitial garnet and pyroxene, (2) garnet+pyroxene aggregate with Ti-clinohumite inclusions, and (3) Ti-clinohumite-free aggregate dominated by garnet. Apatite, phlogopite, zircon, hematite, pentlandite, and an unknown Ni-Fe-volatile-Si (NFVS) mineral, which is replaced by Ni-greenalite, occur as accessories. Serpentine is the major secondary mineral. Garnet (Prp_63.9–64.6Alm_25.8–26.9Grs_1.4–7.9Uva_0.5–7.6Sps_1.0) in all three aggregates is pyrope-rich with very low grossular component, with that in the aggregate (2) most enriched in Cr (Cr₂O₃=2.55 wt.%). Orthopyroxene is depleted in Al (Al₂O₃=0.16 wt.% in the cores) and Ca (CaO=0.06–0.09 wt.% in the cores), with X_Mg (Mg/(Mg+Fe)) values at ca. 0.900. Clinopyroxene is chromian diopside with Fe³⁺≥Fe²⁺. Matrix clinopyroxene has a lower X_Mg (0.862) than that (0.887) included in Ti-clinohumite. The rock contains modest amount of heavy rare earth elements (HREE) (10 to 12×C1 chondrite), with significant enrichment in Cr, Co, Ni, V, Sr, and light rare earth elements (LREE) (22 to 33×C1 chondrite). The clinopyroxene is very enriched in Cr (Cr₂O₃ is up to 2.09 wt.% in the cores) and Sr (ca. 350 ppm) and LREE (Ce_N/Yb_N=157.7). Ti-clinohumite is enriched in Ni (1981 ppm), Co (123 ppm), and Nb (85 ppm).

While it is possible to enrich ultramafites in incompatible elements in a subducted slab, the high Al, Fe, Ti, and low Si, Ca, and Na contents in the Ti-clinohumite rock are difficult to account for by crustal metasomatism of an ultramafite. On the other hand, the similarity in major and trace element compositions and their systematic variations between the Ti-clinohumite-garnet-pyroxene rock of this study and those of Mg-metasomatised Fe–Ti gabbros reported in the literature suggest that crustal metasomatism occurred in a gabbroic protolith, which resulted in addition of Cr, Co, Ni, and Mg and removal of Si, Ca, Na, Al, and Fe. This implies that the rock was in contact with an ultramafite at low pressure. During subsequent subduction, the metagabbro was thrust into the country gneiss, where gneiss-derived hydrous fluids caused enrichment of Sr and LREE in recrystallised clinopyroxene. P–T estimates for the high-pressure assemblage are ca. 4.2 GPa and ca. 760 °C, compatible with those for the eclogites and gneisses in this terrane. It is possible that the Ti-clinohumite-garnet-pyroxene rock and associated eclogites represent remnants of former oceanic crust that was subducted to a great depth.  相似文献   

Spinel–sapphirine–quartz bearing composite inclusion within garnet from an ultrahigh-temperature pelitic granulite: Implications for metamorphic history and P–T path     

Toshiaki Tsunogae  M. Santosh 《Lithos》2006,92(3-4):524-536

We report here a multiphase mineral inclusion composed of quartz, plagioclase, K-feldspar, sapphirine, spinel, orthopyroxene, and biotite, in porphyroblastic garnet within a pelitic granulite from Rajapalaiyam in the Madurai Granulite Block, southern India. In this unique textural association, hitherto unreported in previous studies, sapphirine shows four occurrences: (1) as anhedral mineral between spinel and quartz (Spr-1), (2) subhedral to euhedral needles mantled by quartz (Spr-2), (3) subhedral to anhedral mineral in orthopyroxene, and (4) isolated inclusion with quartz (Spr-4). Spr-1, Spr-2, and Spr-4 show direct grain contact with quartz, providing evidence for ultrahigh-temperature (UHT) metamorphism at temperatures exceeding 1000 °C. Associated orthopyroxene shows high Mg/(Fe + Mg) ratio ( 0.75) and Al₂O₃ content (up to 9.6 wt.%), also suggesting T > 1050 °C and P > 10 kbar during peak metamorphism.

Coarse spinel (Spl-1) with irregular grain morphology and adjacent quartz grains are separated by thin films of Spr-1 and K-feldspar, suggesting that Spl-1 and quartz were in equilibrium before the stability of Spr-1 + quartz. This texture implies that the P–T conditions of the rock shifted from the stability field of spinel + quartz to sapphirine + quartz. Petrogenetic grid considerations based on available data from the FMAS system favour exhumation along a counterclockwise P–T trajectory. The irregular shape of the inclusion and chemistry of the inclusion minerals are markedly different from the matrix phases suggesting the possibility that the inclusion minerals could have equilibrated from cordierite-bearing silicate-melt pockets during the garnet growth at extreme UHT conditions.  相似文献   

Carbonatite melt–CO₂ fluid inclusions in mantle xenoliths from Tenerife, Canary Islands: a story of trapping, immiscibility and fluid–rock interaction in the upper mantle     

Maria Luce Frezzotti  Tom Andersen  Else-Ragnhild Neumann  Siri Lene Simonsen 《Lithos》2002,64(3-4):77-96

Three types of fluid inclusions have been identified in olivine porphyroclasts in the spinel harzburgite and lherzolite xenoliths from Tenerife: pure CO₂ (Type A); carbonate-rich CO₂–SO₂ mixtures (Type B); and polyphase inclusions dominated by silicate glass±fluid±sp±silicate±sulfide±carbonate (Type C). Type A inclusions commonly exhibit a “coating” (a few microns thick) consisting of an aggregate of a platy, hydrous Mg–Fe–Si phase, most likely talc, together with very small amounts of halite, dolomite and other phases. Larger crystals (e.g. (Na,K)Cl, dolomite, spinel, sulfide and phlogopite) may be found on either side of the “coating”, towards the wall of the host mineral or towards the inclusion center. These different fluids were formed through the immiscible separations and fluid–wall-rock reactions from a common, volatile-rich, siliceous, alkaline carbonatite melt infiltrating the upper mantle beneath the Tenerife. First, the original siliceous carbonatite melt is separated from a mixed CO₂–H₂O–NaCl fluid and a silicate/silicocarbonatite melt (preserved in Type A inclusions). The reaction of the carbonaceous silicate melt with the wall-rock minerals gave rise to large poikilitic orthopyroxene and clinopyroxene grains, and smaller neoblasts. During the metasomatic processes, the consumption of the silicate part of the melt produced carbonate-enriched Type B CO₂–SO₂ fluids which were trapped in exsolved orthopyroxene porphyroclasts. At the later stages, the interstitial silicate/silicocarbonatite fluids were trapped as Type C inclusions. At a temperature above 650 °C, the mixed CO₂–H₂O–NaCl fluid inside the Type A inclusions were separated into CO₂-rich fluid and H₂O–NaCl brine. At T<650 °C, the residual silicate melt reacted with the host olivine, forming a reaction rim or “coating” along the inclusion walls consisting of talc (or possibly serpentine) together with minute crystals of NaCl, KCl, carbonates and sulfides, leaving a residual CO₂ fluid. The homogenization temperatures of +2 to +25 °C obtained from the Type A CO₂ inclusions reflect the densities of the residual CO₂ after its reactions with the olivine host, and are unrelated to the initial fluid density or the external pressure at the time of trapping. The latter are restricted by the estimated crystallization temperatures of 1000–1200 °C, and the spinel lherzolite phase assemblage of the xenolith, which is 0.7–1.7 GPa.  相似文献   

Experimental study of the joins forsterite–diopside–leucite– and forsterite–leucite–åkermanite up to 2.3 GPa [P(H₂O) = P(Total)] and variable temperatures: Its petrological significance     

Kaustav Nag  Makoto Arima  Alok K. Gupta 《Lithos》2007,98(1-4):177-194

We conducted a series of melting experiments in the join forsterite–diopside–leucite under 0.1 and 2.3 GPa and in the join forsterite–leucite–åkermanite under 2.3 GPa to understand paragenetic relationships amongst different types of lamproitic and lamprophyric magmas with K-rich mafic and ultramafic volcanic (kamafugitic) rocks. Both the joins were studied in the presence of excess water. The experimental results of the join forsterite–diopside–leucite at 0.1 GPa show that the five-phase point of forsterite (Fo)_ss + diopside (Di)_ss + leucite (Lc)_ss + liquid (Liq) + vapour (V) (equivalent to ugandite lava) occurs at Fo₂Di₅₀Lc₄₈ at 880 ± 5 °C. Phlogopite appears as the last phase at 830 ± 15 °C. The final crystalline assemblage of forsterite_ss + diopside_ss + leucite_ss + phlogopite is similar to the phenocryst assemblage of missourite lava. Present study suggests that an olivine leucitite (ugandite) can be derived from an olivine italite, a slightly potassic peridotite and a leucitite magma.

A study of the join Fo–Di–Lc [P(H₂O) = P(Total)] at 2.3 GPa shows that liquid compositions penetrate the primary phase volumes of forsterite_ss, phlogopite_ss, kalsilitess, K-feldspar_ss and diopside_ss. It has the following three five-phase points: 1) one occurring at Fo₉Di₄₉Lc₄₂ and 1005 ± 5 °C, where liquid and vapour coexists with forsterite_ss, phlogopite_ss and diopside_ss (phlogopite-bearing madupite), 2) the second one at Fo₄Di₅₀Lc₄₆ and 990 ± 10 °C, where diopside_ss, K-feldspar_ss and phlogopite_ss coexist with liquid and vapour (pyroxene-bearing minette), and 3) the third one at Fo₃Di₂₁Lc₇₆ and 775 ± 5 °C, where phlogopite_ss, kalsilite_ss and K-feldspar_ss are in equilibrium with liquid plus vapour (kalsilite-bearing minette).

The experimental results of the join Fo–Lc–åkermanite (Ak) show that the join 40 penetrates the primary phase volumes of forsterite_ss, phlogopite_ss, kalsilite, K-feldspar_ss, diopside_ss and merwinite_ss. The data indicate the presence of four five-phase points: 1) one occurring at Fo₇Lc₄₂Ak₅₁ and 1165 ± 5 °C, where phlogopite_ss, forsterite_ss, diopside_ss coexists with liquid and vapour (olivine-bearing madupite), 2) the second one at Fo₃Lc₄₉Ak₄₈ and 1140 ± 10 °C, where a liquid is in equilibrium with phlogopite_ss, K-feldspar_ss, diopside_ss and vapour (pyroxene-bearing minette), 3) the third one at Fo₁₈Lc₂₁Ak₆₁ and 1255 ± 10 °C, where merwinite_ss, forsterite_ss and diopside_ss are in equilibrium with liquid and vapour (merwinite-bearing wherlite), and 4) the fourth one at Fo₅Lc_73.5Ak_21.5 and 770 ± 5 °C, where kalsilite_ss, phlogopite_ss and K-feldspar coexist with liquid and vapour (kalsilite-bearing minette). The present data suggest that high pressure heteromorphic equivalent of a katungite magma is represented by a kalsilite-bearing minette, a pyroxene-bearing minette, or an olivine-bearing madupite.  相似文献   

Fluid inclusions in granulites, granulitized eclogites and garnet clinopyroxenites from the Dabie–Sulu terranes, eastern China     

Bin Fu  Jacques L.R Touret  Yong-Fei Zheng  Bor-ming Jahn 《Lithos》2003,70(3-4):293-319

Minor granulites (believed to be pre-Triassic), surrounded by abundant amphibolite-facies orthogneiss, occur in the same region as the well-documented Triassic high- and ultrahigh-pressure (HP and UHP) eclogites in the Dabie–Sulu terranes, eastern China. Moreover, some eclogites and garnet clinopyroxenites have been metamorphosed at granulite- to amphibolite-facies conditions during exhumation. Granulitized HP eclogites/garnet clinopyroxenites at Huangweihe and Baizhangyan record estimated eclogite-facies metamorphic conditions of 775–805 °C and ≥15 kbar, followed by granulite- to amphibolite-facies overprint of ca. 750–800 °C and 6–11 kbar. The presence of (Na, Ca, Ba, Sr)-feldspars in garnet and omphacite corresponds to amphibolite-facies conditions. Metamorphic mineral assemblages and P–T estimates for felsic granulite at Huangtuling and mafic granulite at Huilanshan indicate peak conditions of 850 °C and 12 kbar for the granulite-facies metamorphism and 700 °C and 6 kbar for amphibolite-facies retrograde metamorphism. Cordierite–orthopyroxene and ferropargasite–plagioclase coronas and symplectites around garnet record a strong, rapid decompression, possibly contemporaneous with the uplift of neighbouring HP/UHP eclogites.

Carbonic fluid (CO₂-rich) inclusions are predominant in both HP granulites and granulitized HP/UHP eclogites/garnet clinopyroxenites. They have low densities, having been reset during decompression. Minor amounts of CH₄ and/or N₂ as well as carbonate are present. In the granulitized HP/UHP eclogites/garnet clinopyroxenites, early fluids are high-salinity brines with minor N₂, whereas low-salinity fluids formed during retrogression. Syn-granulite-facies carbonic fluid inclusions occur either in quartz rods in clinopyroxene (granulitized HP garnet clinopyxeronite) or in quartz blebs in garnet and quartz matrices (UHP eclogite). For HP granulites, a limited number of primary CO₂ and mixed H₂O–CO₂(liquid) inclusions have also been observed in undeformed quartz inclusions within garnet, orthopyroxene, and plagioclase which contain abundant, low-density CO₂±carbonate inclusions. It is suggested that the primary fluid in the HP granulites was high-density CO₂, mixed with a significant quantity of water. The water was consumed by retrograde metamorphic mineral reactions and may also have been responsible for metasomatic reactions (“giant myrmekites”) occurring at quartz–feldspar boundaries. Compared with the UHP eclogites in this region, the granulites were exhumed in the presence of massive, externally derived carbonic fluids and subsequently limited low-salinity aqueous fluids, probably derived from the surrounding gneisses.  相似文献   

Coesite inclusions and prograde compositional zonation of garnet in whiteschist of the HP-UHPM Kokchetav massif, Kazakhstan: a record of progressive UHP metamorphism   总被引：3，自引：0，他引：3  

Chris D. Parkinson   《Lithos》2000,52(1-4):215-233

Coarse-grained whiteschist, containing the assemblage: garnet+kyanite+phengite+talc+quartz/coesite, is an abundant constituent of the ultrahigh-pressure metamorphic (UHPM) belt in the Kulet region of the Kokchetav massif of Kazakhstan.

Garnet displays prograde compositional zonation, with decreasing spessartine and increasing pyrope components, from core to rim. Cores were recrystallized at T=380°C (inner) to 580°C (outer) at P<10 kbar (garnet–ilmenite geothermometry, margarite+quartz stability), and mantles at T=720–760°C and P_H20=34–36 kbar (coesite+graphite stability, phengite geobarometer, KFMASH system reaction equilibria). Textural evidence indicates that rims grew during decompression and cooling, within the Qtz-stability field.

Silica inclusions (quartz and/or coesite) of various textural types within garnets display a systematic zonal distribution. Cores contain abundant inclusions of euhedral quartz (type 1 inclusions). Inner mantle regions contain inclusions of polycrystalline quartz pseudomorphs after coesite (type 2), with minute dusty micro-inclusions of chlorite, and more rarely, talc and kyanite in their cores; intense radial and concentric fractures are well developed in the garnet. Intermediate mantle regions contain bimineralic inclusions with coesite cores and palisade quartz rims (type 3), which are also surrounded by radial fractures. Subhedral inclusions of pure coesite without quartz overgrowths or radial fractures (type 4) occur in the outer part of the mantle. Garnet rims are silica-inclusion-free.

Type 1 inclusions in garnet cores represent the low-P, low-T precursor stage to UHPM recrystallization, and attest to the persistence of low-P assemblages in the coesite-stability field. Coesites in inclusion types 2, 3, and 4 are interpreted to have sequentially crystallized by net transfer reaction (kyanite+talc=garnet+coesite+H₂O), and were sequestered within the garnet with progressively decreasing amounts of intragranular aqueous fluid.

During the retrograde evolution of the rock, all three inclusion types diverged from the host garnet P–T path at the coesite–quartz equilibrium, and followed a trajectory parallel to the equilibrium boundary resulting in inclusion overpressure. Coesite in type 2 inclusions suffered rapid intragranular H₂O-catalysed transformation to quartz, and ruptured the host garnet at about 600°C (when inclusion P27 kbar, garnet host P9 kbar). Instantaneous decompression to the host garnet P–T path, passed through the kyanite+talc=chlorite+quartz reaction equilibrium, resulting in the dusty micro-assemblage in inclusion cores. Type 3 inclusions suffered a lower volumetric proportion transformation to quartz at the coesite–quartz equilibrium, and finally underwent rupture and decompression when T<400°C, facilitating coesite preservation. Type 4 coesite inclusions are interpreted to have suffered minimal transformation to quartz and proceeded to surface temperature conditions along or near the coesite–quartz equilibrium boundary.  相似文献   

First Report of Sapphirine+Quartz Assemblage from Southern India: Implications for Ultrahigh-temperature Metamorphism   总被引：1，自引：0，他引：1  

Keiko Tateishi  Toshiaki Tsunogae  M. Santosh  A.S. Janardhan 《Gondwana Research》2004,7(4):899-912

We report here for the first time, the occurrence of sapphirine+quartz assemblage in textural equilibrium from quartzo-feldspathic and pelitic granulites from southern India. The sapphirine-bearing rocks occur as layered gneisses associated with pink granite within massive charnockite in Rajapalaiyam area in the southern part of Madurai Block. Sapphirine occurs in three associations: (i) fine-grained subhedral mineral associated with quartz enclosed in garnet, (ii) intergrowth with Al-rich orthopyroxene (up to 9.7 wt.% Al₂O₃), and (iii) in symplectitic intergrowth with orthopyroxene (Al₂O₃= 5.9–6.7 wt.%) and cordierite surrounding garnet. The sapphirine in association with quartz is slightly magnesian (X_Mg = 0.79–0.80) and low in Si content (1.55–1.56 pfu) as compared with those associated with orthopyroxene and cordierite (X_Mg= 0.77–0.79, Si = 1.59–1.63 pfu). The sapphirine+quartz assemblage suggests that the granulites underwent T>1050 °C peak metamorphism. Cores of porphyroblastic orthopyroxene in the sapphirine-bearing rocks shows high-Al₂O₃ content of up to 9.7 wt.%, suggesting T = 1040–1060°C and P = 8 kbar. FMAS reaction of sapphirine+quartz→garnet+sillimanite+cordierite indicates a cooling from sapphirine+quartz stability field after the peak ultrahigh-temperature metamorphism. Slightly lower temperature estimates from ternary feldspar and sapphirine-spinel geothermometers (T = 950–1000°C) also support a post-peak isobaric cooling. Corona textures of orthopyroxene+cordierite (±sapphirine), orthopyroxene+sapphirine, and cordierite+spinel around garnet suggest subsequent decompression. The sapphirine-quartz association and related textures reported in this study have important bearing on the ultrahigh-temperature metamorphism and exhumation history of the Madurai Block as well as on the tectonic evolution of the continental deep crust in southern India.  相似文献   

A hydrothermal investigation of the system FeO, Fe₂O₃, TiO₂     

Anders Lindh 《Lithos》1972,5(4):325-343

Phase relations in the system FeO---Fe₂O₃---TiO₂, at temperatures ranging between 300°C and 700°C, have been investigated experimentally with special refference to the reaction Fe₃O₄ + TiO₂ = Fe₂O₃ + FeTiO₃. Pressure was varied between 500 and 2000 bars but its effect was negligible. Magnetite and rutile are the stable assemblage at temperatures above 550 dgC, and hematite and ilmenite are stable for lower temperatures. The equilibrium oxygen fugacity is estimated to be 10^−17.5 bars at equilibrium temperature. It is suggested that intermediate hematite-ilmenite solid solutions are inhomogeneous, consisting of ‘domains’ of hematite and ilmenite. The ‘domains’ are too small to be resolved by X-ray diffraction techniques. The top of the solvus curve in the hematite-ilmenite solution corresponds to a temperature of 660°C. Regular solution theory is not applicable to the solid solution.  相似文献   

Reactions and textures in grossular–wollastonite–scapolite calc–silicate granulites from Maligawila, Sri Lanka: evidence for high-temperature isobaric cooling in the meta-sediments of the Highland Complex     

V. Mathavan  G. W. A. R. Fernando   《Lithos》2001,59(4):217-232

Grossular–wollastonite–scapolite calc–silicate granulites from Maligawila in the Buttala klippe, which form part of the overthrusted rocks of the Highland Complex of Sri Lanka, preserve a number of spectacular coronas and replacement textures that could be effectively used to infer their P–T–fluid history. These textures include coronas of garnet, garnet–quartz, and garnet–quartz–calcite at the grain boundaries of wollastonite, scapolite, and calcite as well as calcite–plagioclase and calcite–quartz symplectites or finer grains after scapolite and wollastonite respectively. Other textures include a double rind of coronal scapolite and coronal garnet between matrix garnet and calcite. The reactions that produced these coronas and replacement textures, except those involving clinopyroxene, are modelled in the CaO–Al₂O₃–SiO₂–CO₂ system using the reduced activities. Calculated examples of T–X_CO2 and P–X_CO2 projections indicate that the peak metamorphic temperature of about 900–875 °C at a pressure of 9 kbar and the peak metamorphic fluid composition is constrained to be low in X_CO2 (0.1<X_CO2<0.30). Interpretation of the textural features on the basis of the partial grids revealed that the calc–silicate granulites underwent high-temperature isobaric cooling, from about 900–875 °C to a temperature below 675 °C, following the peak metamorphism. The late-stage cooling was accompanied by an influx of hydrous fluids. The calc–silicate granulites provide evidence for high-temperature isobaric cooling in the meta-sediments of the Highland Complex, earlier considered by some workers to be confined exclusively to the meta-igneous rocks. The coronal scapolite may have formed under open-system metasomatism.  相似文献   

The Homestead kimberlite, central Montana, USA: mineralogy, xenocrysts, and upper-mantle xenoliths     

B. Carter Hearn Jr.   《Lithos》2004,77(1-4):473-491

The Homestead kimberlite was emplaced in lower Cretaceous marine shale and siltstone in the Grassrange area of central Montana. The Grassrange area includes aillikite, alnoite, carbonatite, kimberlite, and monchiquite and is situated within the Archean Wyoming craton. The kimberlite contains 25–30 modal% olivine as xenocrysts and phenocrysts in a matrix of phlogopite, monticellite, diopside, serpentine, chlorite, hydrous Ca–Al–Na silicates, perovskite, and spinel. The rock is kimberlite based on mineralogy, the presence of atoll-textured groundmass spinels, and kimberlitic core-rim zoning of groundmass spinels and groundmass phlogopites.

Garnet xenocrysts are mainly Cr-pyropes, of which 2–12% are G10 compositions, crustal almandines are rare and eclogitic garnets are absent. Spinel xenocrysts have MgO and Cr₂O₃ contents ranging into the diamond inclusion field. Mg-ilmenite xenocrysts contain 7–11 wt.% MgO and 0.8–1.9 wt.% Cr₂O₃, with (Fe⁺³/Fe^tot) from 0.17–0.31. Olivine is the only obvious megacryst mineral present. One microdiamond was recovered from caustic fusion of a 45-kg sample.

Upper-mantle xenoliths up to 70 cm size are abundant and are some of the largest known garnet peridotite xenoliths in North America. The xenolith suite is dominated by dunites, and harzburgites containing garnet and/or spinel. Granulites are rare and eclogites are absent. Among 153 xenoliths, 7% are lherzolites, 61% are harzburgites, 31% are dunites, and 1% are orthopyroxenites. Three of 30 peridotite xenoliths that were analysed are low-Ca garnet–spinel harzburgites containing G10 garnets. Xenolith textures are mainly coarse granular, and only 5% are porphyroclastic.

Xenolith modal mineralogy and mineral compositions indicate ancient major-element depletion as observed in other Wyoming craton xenolith assemblages, followed by younger enrichment events evidenced by tectonized or undeformed veins of orthopyroxenite, clinopyroxenite, websterite, and the presence of phlogopite-bearing veins and disseminated phlogopite. Phlogopite-bearing veins may represent kimberlite-related addition and/or earlier K-metasomatism.

Xenolith thermobarometry using published two-pyroxene and Al-in-opx methods suggest that garnet–spinel peridotites are derived from 1180 to 1390 °C and 3.6 to 4.7 GPa, close to the diamond–graphite boundary and above a 38 mW/m² shield geotherm. Low-Ca garnet–spinel harzburgites with G10 garnets fall in about the same T and P range. Most spinel peridotites with assumed 2.0 GPa pressure are in the same T range, possibly indicating heating of the shallow mantle. Four of 79 Cr diopside xenocrysts have P–T estimates in the diamond stability field using published single-pyroxene P–T calculation methods.  相似文献   

Tracing high-pressure metamorphism in marbles: Phase relations in high-grade aluminous calcite–dolomite marbles from the Greek Rhodope massif in the system CaO–MgO–Al₂O₃–SiO₂–CO₂ and indications of prior aragonite     

A. Proyer  E. Mposkos  I. Baziotis  G. Hoinkes 《Lithos》2008,104(1-4):119-130

Four different types of parageneses of the minerals calcite, dolomite, diopside, forsterite, spinel, amphibole (pargasite), (Ti–)clinohumite and phlogopite were observed in calcite–dolomite marbles collected in the Kimi-Complex of the Rhodope Metamorphic Province (RMP). The presence of former aragonite can be inferred from carbonate inclusions, which, in combination with an analysis of phase relations in the simplified system CaO–MgO–Al₂O₃–SiO₂–CO₂ (CMAS–CO₂) show that the mineral assemblages preserved in these marbles most likely equilibrated at the aragonite–calcite transition, slightly below the coesite stability field, at ca. 720 °C, 25 kbar and a_CO2 ~ 0.01. The thermodynamic model predicts that no matter what activity of CO₂, garnet has to be present in aluminous calcite–dolomite-marble at UHP conditions.  相似文献   

Mineral chemistry and thermobarometry of inclusions from De Beers Pool diamonds, Kimberley, South Africa     

D. Phillips  J.W. Harris  K.S. Viljoen 《Lithos》2004,77(1-4):155-179

Silicate and oxide mineral inclusions in diamonds from the geologically and historically important De Beers Pool kimberlites in Kimberley, South Africa, are characterised by harzburgitic compositions (>90%), with lesser abundances from eclogitic and websteritic parageneses. The De Beers Pool diamonds contain unusually high numbers of inclusion intergrowths, with garnet+orthopyroxene±chromite±olivine and chromite+olivine assemblages dominant. More unusual intergrowths include garnet+olivine+magnesite and an eclogitic assemblage comprising garnet+clinopyroxene+rutile. The mineral chemistry of the De Beers Pool inclusions overlaps that of most worldwide localities. Peridotitic garnet inclusions exhibit variable CaO (<5.8 wt.%) and Cr₂O₃ contents (3.0–15.0 wt.%), although the majority are harzburgitic with very low calcium concentrations (<2 wt.% CaO). Eclogitic garnet inclusions are characterised by a wide range in CaO (3.3–21.1 wt.%) with low Cr₂O₃ (<1 wt.%). Websteritic garnets exhibit intermediate compositions. Most chromite inclusions contain 63–67 wt.% Cr₂O₃ and <0.5 wt.% TiO₂. Olivine and orthopyroxene inclusions are magnesium-rich with Mg-numbers of 93–97. Olivine inclusions in chromite exhibit the highest Mg-numbers and also contain elevated Cr₂O₃ contents up to 1.0 wt.%. Peridotitic clinopyroxene inclusions are Cr-diopsides with up to 0.8 wt.% K₂O. Eclogitic and websteritic clinopyroxene inclusions exhibit overlapping compositions with a wide range in Mg-numbers (66–86).

Calculated temperatures for non-touching inclusion pairs from individual diamonds range from 1082 to 1320 °C (average=1197 °C), whereas pressures vary from 4.6 to 7.7 GPa (average=6.3 GPa). Touching inclusion assemblages are characterised by equilibration temperatures of 995 to 1182 °C (average=1079 °C) and pressures of 4.2–6.8 GPa (average=5.4 GPa). Provided that the non-touching inclusions represent equilibrium assemblages, it is suggested that these inclusions record the conditions at the time of diamond crystallisation (1200 °C; 3.0 Ga). The lower average temperatures for touching inclusions are attributed to re-equilibration in a cooling mantle (1050 °C) prior to kimberlite eruption at 85 Ma. Pressure estimates for touching garnet–orthopyroxene inclusions are also skewed towards lower values than most non-touching inclusions. This apparent difference may be an artefact of the Al-exchange geobarometer and/or the result of sampling bias, due to limited numbers of non-touching garnet–orthopyroxene inclusions. Alternatively pressure differences could be caused by differential uplift in the mantle or possibly variations in thermal compressibility between diamond and silicate inclusions. However, thermodynamic modelling suggests that thermal compressibility differences would cause only minor changes in internal inclusion pressures (<0.2 GPa/100 °C).  相似文献   

Petrogenesis of Al–silicate-bearing trondhjemitic migmatites from NE Sardinia, Italy     

Gabriele Cruciani  Marcello Franceschelli  Franco Marco Elter  Mariano Puxeddu  Daniela Utzeri 《Lithos》2008,102(3-4):554-574

The migmatites from Punta Sirenella (NE Sardinia) are layered rocks containing 3–5 vol.% of centimeter-sized stromatic leucosomes which are mainly trondhjemitic and only rarely granitic in composition. They underwent three deformation phases, from D₁ to D₃. The D₁ deformation shows a top to the NW shear component followed by a top to the NE/SE component along the XZ plane of the S₂ schistosity. Migmatization started early, during the compressional and crustal thickening stage of Variscan orogeny and was still in progress during the following extensional stage of unroofing and exhumation.

The trondhjemitic leucosomes, mainly consisting of quartz, plagioclase, biotite ± garnet ± kyanite ± fibrolite, retrograde muscovite and rare K-feldspar, are locally bordered by millimeter-sized biotite-rich melanosomes. The rare granitic leucosomes differ from trondhjemitic ones only in the increase in modal content of K-feldspar, up to 25%. Partial melting started in the kyanite field at about 700–720 °C and 0.8–0.9 GPa, and was followed by re-equilibration at 650–670 °C and 0.4–0.6 GPa, producing fibrolite–biotite intergrowth and coarse-grained muscovite.

The leucosomes have higher SiO₂, CaO, Na₂O, Sr and lower Al₂O₃, Fe₂O₃, MgO, TiO₂, K₂O, P₂O₅, Rb, Ba, Cr, V, Zr, Nb, Zn and REE content with respect to proximal hosts and pelitic metagreywackes. Sporadic anomalous high content of calcium and ferromagnesian elements in some leucosomes is due to entrainment of significant amounts of restitic plagioclase, biotite and accessory phases. The rare granitic leucosomes reveal peritectic K-feldspar produced by muscovite-dehydration melting. Most leucosomes show low REE content, moderately fractionated REE patterns and marked positive Eu anomaly. Proximal hosts and pelitic metagraywackes are characterized by higher REE content, more fractionated REE patterns and slightly negative Eu anomaly.

The trondhjemitic leucosomes were generated by H₂O-fluxed melting at 700 °C of a greywacke to pelitic–greywacke metasedimentary source-rock. The disequilibrium melting process is the most reliable melting model for Punta Sirenella leucosomes.  相似文献   

The interpretation of reaction textures in Fe‐rich metapelitic granulites of the Musgrave Block,central Australia: constraints from mineral equilibria calculations in the system K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3     

R. W. White  Roger Powell  G. L. Clarke 《Journal of Metamorphic Geology》2002,20(1):41-55

Fe‐rich metapelitic granulites of the Musgrave Block, central Australia, contain several symplectic and coronal reaction textures that post‐date a peak S2 metamorphic assemblage involving garnet, sillimanite, spinel, ilmenite, K‐feldspar and quartz. The earliest reaction textures involve spinel‐ and quartz‐bearing symplectites that enclose garnet and to a lesser extent sillimanite. The symplectic spinel and quartz are in places separated by later garnet and/or sillimanite coronas. The metamorphic effects of a later, D3, event are restricted to zones of moderate to high strain where a metamorphic assemblage of garnet, sillimanite, K‐feldspar, magnetite, ilmenite, quartz and biotite is preserved. Quantitative mineral equilibria calculations in the system K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–Fe₂O₃ (KFMASHTO) using Thermocalc 3.0 and the accompanying internally consistent dataset provide important constraints on the influence of TiO₂ and Fe₂O₃ on biotite‐bearing and spinel‐bearing equilibria, respectively. Biotite‐bearing equilibria are shifted to higher temperatures and spinel‐bearing equilibria to higher pressures and lower temperatures in comparison to the equivalent equilibria in K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O (KFMASH). The sequence of reaction textures involving spinel is consistent with a D2 P–T path that involved a small amount of decompression followed predominantly by cooling within a single mineral assemblage stability field. Thus, the reaction textures reflect changes in modal proportions within an equilibrium assemblage rather than the crossing of a univariant reaction. The D3 metamorphic assemblage is consistent with lower temperatures than those inferred for D2.  相似文献   

Prograde garnet-bearing ultramafic rocks from the Tromsø Nappe, northern Scandinavian Caledonides     

Erling J.K. Ravna  Kre Kullerud  Edel Ellingsen 《Lithos》2006,92(3-4):336-356

Garnet-bearing peridotitic rocks closely associated with eclogite within the Tromsø Nappe of the northern Scandinavian Caledonides show good evidence for prograde metamorphism. Early stages are recognized as inclusions of hornblende and chlorite in the cores of large garnet poikiloblasts. Closer to the garnet rim, clinopyroxene and Cr-poor spinel appear as additional inclusion phases. Four suites of spinel inclusions can be distinguished based on optical properties and chemical composition. The innermost suite (suite 1) has the lowest Cr# and highest Mg#. Further rimward, the spinel inclusions gradually change in composition, with increasing Cr# and decreasing Mg#. Spinel is rare in the matrix, but locally chromitic spinel occurs as larger grains. Garnet poikiloblasts are rimmed by a kelyphite zone consisting of Hbl + Cr-poor Spl or Opx ± Cpx + Cr-poor Spl, and locally an inner zone of Na-rich Hbl + Chl. Matrix assemblage in the garnet-bearing peridotitic rocks is Hbl + Chl + Cpx + Ol ± Cr-rich spinel, defining a strong foliation wrapping around garnets and associated kelyphites. Thin layers of garnet-orthopyroxenite and garnet–hornblende–zoisite–chlorite rocks are presumably coeval with the matrix foliation of the peridotitic rocks.

In dunitic to harzburgitic compositions large undulatory grains of Ol + Opx ± Chl + Spl apparently define the maximum-P conditions. This assemblage is succeeded by a recrystallized assemblage of Ol ± Tlc ± Mgs, which in turn is overgrown by strain-free poikiloblasts of orthopyroxene, indicating a temperature increase. This is postdated by Tlc + Ath ± Mgs, and finally serpentine.

P–T estimates for the inclusion suites of clinopyroxene and spinel in garnet clearly indicate garnet growth and spinel consumption in a regime of increasing P. The inner suite (suite 1) apparently was in equilibrium with garnet, clinopyroxene and olivine at 1.40 GPa, 675 °C, whereas included spinel with maximum Cr# (suite 4) indicate 2.40 GPa at 740 °C. Grt + Opx from garnet-orthopyroxenite give 1.5–1.9 GPa at 740–770 °C, and Grt + Hbl + Zo + Chl from a zoisite-rich rock give 1.75 ± 0.25 GPa at 740 ± 30 °C, interpreted to represent recrystallization during uplift. In dunitic to harzburgitic compositions, early Ol + Opx ± Chl + Spl is succeeded by Ol ± Tlc ± Mgs, which in turn is overgrown by neoblasts of strain-free orthopyroxene, indicating temperature increase. This is postdated by Tlc + Ath ± Mgs, and finally serpentine.

The ultramafic rocks in the Tromsø Nappe were locally strongly hydrated before subduction along with associated eclogites and metasedimentary rocks during the early (Ordovician) stages of the Caledonian orogeny.  相似文献   

The origin of garnet and clinopyroxene in “depleted” Kaapvaal peridotites     

Nina S. C. Simon  Gordon J. Irvine  Gareth R. Davies  D. Graham Pearson  Richard W. Carlson 《Lithos》2003,71(2-4):289-322

A detailed petrographic, major and trace element and isotope (Re–Os) study is presented on 18 xenoliths from Northern Lesotho kimberlites. The samples represent typical coarse, low-temperature garnet and spinel peridotites and span a P–T range from 60 to 150 km depth. With the exception of one sample (that belongs to the ilmenite–rutile–phlogopite–sulphide suite (IRPS) suite first described by [B. Harte, P.A. Winterburn, J.J. Gurney, Metasomatic and enrichment phenomena in garnet peridotite facies mantle xenoliths from the Matsoku kimberlite pipe, Lesotho. In: Menzies, M. (Ed.), Mantle metsasomatism. Academic Press, London 1987, 145–220.]), all samples considered here have high Mg# and show strong depletion in CaO and Al₂O₃. They have bulk rock Re depletion ages (T_RD) >2.5 Ga and are therefore interpreted as residua from large volume melting in the Archaean. A characteristic of Kaapvaal xenoliths, however, is their high SiO₂ concentrations, and hence, modal orthopyroxene contents that are inconsistent with a simple residual origin of these samples. Moreover, trace element signatures show strong overall incompatible element enrichment and REE disequilibrium between garnet and clinopyroxene. Textural and subtle major element disequilibria were also observed. We therefore conclude that garnet and clinopyroxene are not co-genetic and suggest that (most) clinopyroxene in the Archaean Kaapvaal peridotite xenoliths is of metasomatic origin and crystallized relatively recently, possibly from a melt precursory to the kimberlite.

Possible explanations for the origin of garnet are exsolution from a high-temperature, Al- and Ca-rich orthopyroxene (indicating primary melt extraction at shallow levels) or a majorite phase (primary melting at >6 GPa). Mass balance calculations, however, show that not all garnet observed in the samples today is of a simple exsolution origin. The extreme LREE enrichment (sigmoidal REE pattern in all garnet cores) is also inconsistent with exsolution from a residual orthopyroxene. Therefore, extensive metasomatism and probably re-crystallization of the lithosphere after melt-depletion and garnet exsolution is required to obtain the present textural and compositional features of the xenoliths. The metasomatic agent that modified or perhaps even precipitated garnet was a highly fractionated melt or fluid that might have been derived from the asthenosphere or from recycled oceanic crust. Since, to date, partitioning of trace elements between orthopyroxene and garnet/clinopyroxene is poorly constrained, it was impossible to assess if orthopyroxene is in chemical equilibrium with garnet or clinopyroxene. Therefore, further trace element and isotopic studies are required to constrain the timing of garnet introduction/modification and its possible link with the SiO₂ enrichment of the Kaapvaal lithosphere.  相似文献