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1.
We have investigated the effect of Fe on the stabilities of carbonate (carb) in lherzolite assemblages by determining the partitioning of Fe and Mg between silicate (olivine; ol) and carbonates (magnesite, dolomite, magnesian calcite) at high pressures and temperatures. Fe enters olivine preferentially relative to magnesite and ordered dolomite, but Fe and Mg partition almost equally between disordered calcic carbonate and olivine. Measurement of K d (X Fe carb X Mg ol /X Fe ol X Mg carb ) as a function of Fe/ Mg ratio indicates that Fe–Mg carbonates deviate only slightly from ideality. Using the regular solution parameter for olivine W FeMg ol of 3.7±0.8 kJ/mol (Wiser and Wood 1991) we obtain for (FeMg)CO3 a W FeMg carb of 3.05±1.50 kJ/mol. The effect of Ca–Mg–Fe disordering is to raise K d substantially enabling us to calculate W CaMg carb -W CaFe carb of 5.3±2.2 kJ/mol. The activity-composition relationships and partitioning data have been used to calculate the effect of Fe/Mg ratio on mantle decarbonation and exchange reactions. We find that carbonate (dolomite and magnesian calcite) is stable to slightly lower pressures (by 1 kbar) in mantle lherzolitic assemblages than in the CaO–MgO–SiO2(CMS)–CO2 system. The high pressure breakdown of dolomite + orthopyroxene to magnesite + clinopyroxene is displaced to higher pressures (by 2 kbar) in natural compositions relative to CMS. CO2. We also find a stability field of magnesian calcite in lherzolite at 15–25 kbar and 750–1000°C.  相似文献   

2.
Temperature and H2O activity can be determined with high precision using metamorphic mineral assemblages that define both a dehydration equilibrium and a temperature-sensitive cation-exchange equilibrium. Such determinations are obtained by applying the Gibbs method and then integrating two resulting differential equations, as illustrated here for the assemblage garnet-chlorite-quartz. The first equation, a geothermometer that monitors temperature based upon Fe–Mg exchange between garnet and chlorite, was calibrated using rocks at Pecos Baldy, New Mexico: 0=0.05 P(bars)–19.02 T(K)+4607 ln K D+24,156 with errors of ±8°C based upon analytical precision. The second equation monitors differences in the activity of water between specimens (1) and (2): 0=(0.1 X Mg–chl, 1 – 2.05)(P 2 – P 1) +[–33.02+5.96 ln(X Fe–chl, 1/X alm, 1)][T 2–T 1 –2.67 RT 1ln[a(H2O)2/a(H2O)1] +5.96 T 1ln(X Fe–chl, 2 X alm, 1/X Fe–chl, 1 X alm, 2).For samples equilibrated at the same pressure and temperature, microprobe analytical errors of 1% limit precision to ±0.01 a(H2O). For samples equilibrated at the same pressure but variable temperature, uncertainty of ±8°C limits precision to ±0.06 a(H2O). Extreme presure sensitivity requires that the H2O-barometer be applied only to rocks where pressure gradients are absent or well-constrained. The geothermometer gives temperatures in agreement with two other garnet-chlorite geothermometers (Dickenson and Hewitt 1986; Ghent et al. 1987) and with garnet-biotite geothermometry (ferry and Spear 1978) over the temperature range 350–520°C. Application of the relative H2O barometer shows variations in the activity of water approaching 0.30 in several study areas. Either pelitic schists commonly equilibrate with a fluid that is not pure H2O, or some pelitic rocks undergo metamorphism in the absence of a free fluid phase.  相似文献   

3.
The diffusion coefficients of Fe2+ and Mg in aluminous spinel at ∼20 kb, 950 to 1325°C, and at 30 kb, 1125°C have been determined via diffusion couple experiments and numerical modeling of the induced diffusion profiles. The oxygen fugacity, fO2, was constrained by graphite encapsulating materials. The retrieved self-diffusion coefficients of Fe2+ and Mg at ∼20 kb, 950 to 1325°C, fit well the Arrhenian relation, D = D0exp(−Q/RT), where Q is the activation energy, with D0(Fe) = 1.8 (±2.8) × 10−5, D0(Mg) = 1.9 (±1.4) × 10−5 cm2/s, Q(Fe) = 198 ± 19, and Q(Mg) = 202 ± 8 kJ/mol. Comparison with the data at 30 kb suggests an activation volume of ∼5 cm3/mol. From analysis of compositional zoning in natural olivine-spinel assemblages in ultramafic rocks, previous reports concluded that D(Fe-Mg) in spinel with Cr/(Cr + Al) ≤0.5 is ∼10 times that in olivine. The diffusion data in spinel and olivine have been applied to the problems of preservation of Mg isotopic inhomogeneity in spinel within the plagioclase-olivine inclusions in Allende meteorite and cooling rates of terrestrial ultramafic rocks.  相似文献   

4.
Garnet-bearing mineral assemblages are commonly observed in pelitic schists regionally metamorphosed to upper greenschist and amphibolite facies conditions. Modelling of thermodynamic data for minerals in the system Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O, however, predicts that garnet should be observed only in rocks of a narrow range of very high Fe/Mg bulk compositions. Traditionally, the nearly ubiquitous presence of garnet in medium- to high-grade pelitic schists is attributed qualitatively to the stabilizing effect of MnO, based on the observed strong partitioning of MnO into garnet relative to other minerals. In order to quantify the dependence of garnet stability on whole-rock MnO content, we have calculated mineral stabilities for pelitic rocks in the system MnO–Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O for a moderate range of MnO contents from a set of non-linear equations that specify mass balance and chemical equilibrium among minerals and fluid. The model pelitic system includes quartz, muscovite. albite, pyrophyllite, chlorite, chloritoid, biotite, garnet, staurolite, cordierite, andalusite, kyanite. sillimanite, K-feldspar and H2O fluid. In the MnO-free system, garnet is restricted to high Fe/Mg bulk compositions, and commonly observed mineral assemblages such as garnet–chlorite and garnet–kyanite are not predicted at any pressure and temperature. In bulk compositions with XMn= Mn/(Fe + Mg + Mn) > 0.01, however, the predicted garnet-bearing mineral assemblages are the same as the sequence of prograde mineral assemblages typically observed in regional metamorphic terranes. Temperatures predicted for the first appearance of garnet in model pelitic schist are also strongly dependent on whole-rock MnO content. The small MnO contents of normal pelitic schists (XMn= 0.01–0.04) are both sufficient and necessary to account for the observed stability of garnet.  相似文献   

5.
Abstract Chloritoid-bearing metasedimentary rocks occur in close proximity to blueschists and eclogites in the Tertiary high-pressure metamorphic belt of northern New Caledonia. The typical assemblage of chloritoid-bearing rocks in the epidote zone is quartzchlorite-muscovite-garnet-chloritoid. In the omphacite zone, epidote is an additional member of the chloritoid-bearing assemblage. Paragonite is rare, plagioclase was not detected, and rutile and ilmenite are the Fe-Ti oxide phases. Chloritoid-glaucophane is not a common assemblage. Chloritoid-bearing rocks have relatively low (Ca+K+Na)/Al ratios and the chloritoids are relatively Mg-rich with Mg/ (Mg+Fe) up to about 0.4. A comparison of the mineral assemblages and mineral chemistry with experimental and computed phase equilibria suggest an upper temperature limit near 560° C in the omphacite zone and a minimum temperature limit near 450° C at 10 kbar. An empirical garnet-chlorite Fe-Mg exchange thermometer does not yield consistent results for the higher-grade rocks, suggesting T s ranging from 390 to 535° C in the omphacite zone and 420–465° C in the epidote zone. The distribution coefficient K D = (Fe/Mg)ctd/(Fe/Mg)chl for chloritoid and chlorite ranges from 3.9 to 6.4, values which are lower than those (=10) from lower greenschist facies rocks, but are near those of upper greenschist facies and albite-epidote amphibolite facies.  相似文献   

6.
Aluminous parageneses containing gedrite, cordierite, garnet, staurolite, biotite, sillimanite, kyanite, quartz or spinel plus corundum are found as dark colored lenses in the polymetamorphic, multideformed Archean complex at Ajitpura in northwest peninsular India. Staurolite, like kyanite, is a relict phase of earlier metamorphism and is excluded as a paragenetic mineral in view of its incompatibility with quartz and gedrite and its lower X Mg values than for garnet of the assemblage. Its stability here is attributed to zinc content of up to 3 wt%. The XMg in other ferromagnesian minerals decreases in the order: cordierite, biotite, gedrite, garnet, as found elsewhere in high grade rocks.The textural criteria and systematic partitioning of Fe and Mg in the ferromagnesian phases, excluding staurolite, indicate attainment of equilibrium during the second metamorphism. From tie line configurations in the phase diagrams, X Mg ratios in the constituent minerals, and other petrographic criteria, it is suggested that gedrite — cordierite-garnet — sillimanite — biotite assemblage has been produced by the reactions: Biotite+Sillimanite+Quartz = Cordierite+Garnet+K-feldspar+Vapor (1) and Biotite+Sillimanite+Quartz = Cordierite +Gedrite+K-feldspar+Vapor (2) which occurred during partial melting of the rocks at fixed P and T conditions.By isothermal P-X(Fe-Mg) sections it has been demonstrated that release of FeO, SiO2 and other components modified the composition of the reactant biotite presumably by the substitution FeSi2 Al, whereby reaction 1 was replaced by reaction 2. Cordierite with higher X Mg was produced with gedrite instead of with garnet, whose X Mg is less than X Mg of gedrite. Reaction 2 has been tentatively located in T-P space from the intersection of some continuous loops in the P-X(Fe-Mg) diagram at 700°C and also by other constraints. The discontinuous reaction 2 is located about 1–2 kilobars higher than reaction 1, which implies that it is difficult to distinguish between effects of pressure and those of melting on the X Mg ratios of the reaction phases.The P-T calibrations of garnet — cordierite, garnet — biotite and garnet — plagioclase equilibria and the calibrations from other dehydration curves give temperatures near 700°C and pressure (assuming ) about 6 kilobars.  相似文献   

7.
We report here that some of the pelitic rocks from the Wanni and Highland Complexes of Sri Lanka reacted with CO2-rich fluids to produce a wide range of unusual secondary carbonate-silicate-oxide-sulphide assemblages. These enable the depth, temperature and fluid compositions of CO2 reactions to be calculated more rigorously than is generally possible for the patches of arrested charnockite that have been described from Sri Lanka. Magnesite-andalusite-quartz has partially replaced primary cordierite, and siderite-rutile replaced ilmenite. Paragenetic sequences involving primary pyrrhotite, ilmenite and magnetite and secondary pyrite-siderite-rutile-magnetite-(hematite) demonstrate the control which carbonate equilibria have upon evolving fluid compositions during cooling. Direct evidence for the role of graphite as a source of CO2 is found in the Highland Complex where primary graphite partially reacted with silicates to form secondary siderite assemblages. It is proposed that following peak metamorphism, continued uplift along a clockwise P-T-t path was accompanied by a series of devolatilization reactions involving breakdown of graphite and the continuous production of secondary CO2-rich fluids. The limited extent of disseminated secondary carbonate reflects the small amount of graphite inferred to have been present in the source rocks. These rocks demonstrate that CO2-rich fluids, as found in disseminated fluid inclusions, need not form during peak granulite metamorphism but may be an inevitable consequence of continued uplift along a clockwise P-T-t path. The arrested charnockite which overprinted some of the hornblende-bearing felsic-intermediate composition rocks in Sri Lanka most likely formed by the same process. Received: 4 May 1994 / Accepted: 25 October 1996  相似文献   

8.
Staurolite and corundum are found as inclusions in tourmaline in a talc-phlogopite-chlorite-albite chist near Mount Bernstein (71°37S, 163°07E), northern Victoria Land, Antarctica. These inclusions are interpreted as relics of a staurolite-talc-corundum-chlorite assemblage that was stable during an early stage in the metamorphic cycle and subsequently armored by tourmaline, probably during the middle stage. Pressures and temperatures during the middle stage are estimated to be 650–700°C and 5.5–6.4 kbar. The transition from the early to the middle stage represents a roughly isothermal decrease in pressure of 2–3 kbar. During a late retrograde stage (T=300–370°C, P=3–5 kbar), staurolite was partly replaced by a muscovitic aggregate containing clinozoisite, pumpellyite, and margarite.The staurolite is unusually Si-poor (26.77, 25.85 weight % SiO2 or 7.275, 7.091 Si per formula unit for 46 oxygens anhydrous), Al-rich (58.00, 57.85% Al2O3, 18.579, 18.702 Al), low in divalent cations (Fe+Mg+Mn+Zn=3.301, 3.560) and magnesian (atomic Mg/(Mg+Fe)=0.42, 0.40). Ion microprobe analysis of the first grain indicates about 0.2% Li2O (0.219 Li) is present. The following substitutions are proposed to explain the unusual chemistry of this staurolite (crystallographic site notation of Smith 1968, in bold letters): Al(Si)+Al(Al(3A,B))Si(Si)+Fe(Fe), Li(Fe)+Al(Al(3A,B))2 Fe(Fe), and 2 Al(Al(3A,B)) 3 Fe(Fe).According to a pressure-temperature diagram constructed by the method of Schreinemakers for the model system FeO-MgO-Al2O3-SiO2 (H2O in excess), the talc-staurolite assemblage should be stable only in quartz-free rocks at temperatures near 700° C and pressures of 8 kbar or more. The rarity of the staurolite-talc assemblage even in Mg-Al-rich rocks metamorphosed at the appropriate pressure-temperature conditions is attributed to the appearance of anthophyllite or, in Na2O-bearing rocks, gedrite. Orthoamphibole-cordierite and orthoamphibolekyanite assemblages with chlorite or corundum are incompatible with staurolite-talc±albite. In rocks lacking corundum and formed at pressures above the stability limit of cordierite, staurolite-talc may be metastable relative to orthoamphibole-kyanite, while in corundum-bearing rocks, staurolite-talc may appear under certain conditions, possibly at higher water activities than the orthoamphibole-kyanite assemblage.  相似文献   

9.
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10.
The East Hebei terrane of North China Craton is characterized by the dome-and-keel structure, a common feature in most Archean cratons, where supracrustal rocks of granulite facies commonly occur as enclaves or rafts in tonalite–trondhjemite–granodiorite (TTG) gneisses. The metamorphic P–T paths of the granulites are significant for addressing the Archean tectonic regimes. Two types of granulite facies paragneiss with pelitic and greywacke compositions from the western margin of Qian'an gneiss dome are documented for their petrography, mineral chemistry, phase equilibria modelling using thermocalc, and zircon dating. Anticlockwise P–T paths involving the pre-peak pressure increase to the ultra-high temperature peak conditions and post-peak cooling and decompression processes were recognized. The pre-peak pressure increase process was constrained for a pelitic granulite mainly based on the spinel and cordierite inclusions in garnet and rutile corona around ilmenite, where the transition from spinel to garnet is modelled at 6–7 kbar at a fixed T = 1,000°C. For greywacke granulite, the pre-peak pressure increase evolution can be ascertained from the textural relation that orthopyroxene is surrounded by garnet, and the outwards increasing grossular (from 0.03 to 0.05) in the core of the atoll-like garnet (Grt-A), to occur from ~7 kbar at ~1,000°C. The peak P–T conditions for pelitic granulite are roughly limited to 7–11 kbar/890–1,050°C on the basis of the stability of the inferred peak assemblage involving garnet, perthite, sillimanite, rutile/ilmenite, and quartz. The peak P–T condition for greywacke granulite can be well constrained as 9–10 kbar/>1,000°C on the basis of the maximum grossular content (XGrs = 0.045–0.050) in the core of subhedral garnet (Grt-B) and the mantle of Grt-A together with an average re-integrated anorthite content (XAn = 0.07) in K-feldspar. The peak temperature condition is consistent with the ternary feldspar thermometer results mostly of 950–1,020°C for antiperthite and perthite in greywacke granulite, and in accordance with the development of oriented needle-like exsolution of Ti±Fe oxides in garnet from pelitic granulite. The post-peak cooling and decompression process was consistent with the decreasing XGrs in the mantle of Grt-A and core of Grt-B in greywacke sample, and the final-stage cooling conditions can be well constrained from the stability of final assemblages marked by the later growth of biotite, as 8–9 kbar/820–880°C for pelitic granulite and 6–9 kbar/840–890°C for greywacke granulite. Zircon dating yields provenance ages from 3.34 to 2.57 Ga and metamorphic ages of c. 2.50 Ga for the two types of granulite. The metamorphic ages overlap the final pulse of the Neoarchean magmatic activity of TTGs that ranges from c. 2.56 to c. 2.48 Ga with a peak at c. 2.52 Ga. Combining the development of dome-and-keel structures, the penecontemporaneity between the metamorphism of supracrustal rocks and TTG magmatic activity, and also the unique anticlockwise P–T paths, we prefer a vertical sagduction regime to interpret the tectonic evolution of the East Hebei terrane, which may be also significant for other Archean cratons.  相似文献   

11.
High-pressure, low-temperature metamorphic Mn-rich quartzites from Andros and Evvia (Euboea) islands, Greece, situated in the Eocene blueschist belt of the Hellenides, reveal different Mn-Al-Ca-Mg-silicate assemblages in response to variable metamorphic grade. On Evvia, piemontite- and/or braunite-rich quartzites which are associated with low-grade blueschists (T<400° C, P> 8 kbar) show the principle mineral assemblage quartz + montite + sursassite + braunite + Mg-chlorite + hematite + rutile + titanite. The Mn-Al-silicate sursassite, basically (Mn2+, Ca)4 Al2(Al, Fe3+, Mn3+, Mg)4Si6O21(OH)7, thus far reported as a rare mineral, locally occurs as a rockforming mineral in cm- to m-thick layers. On Andros, higher-grade quartzites (T450–500° C, P>10 kbar) of similar composition contain the assemblage quartz + piemontite + spessartine + braunite + Mg-chlorite+hematite + phengite+ phlogopite + rutile. Rare sursassite is present only as a relict phase. Additional, mostly accessory minerals in quartzites from Evvia and Andros are ardennite, Na-amphibole, acmitic clinopyroxene, albite, apatite, and tourmaline. The chemical composition of the main phases is characterized in detail.Disequilibrium textures and mineral compositions in some samples from Andros and Evvia imply the reactions sursassite + braunite + quartz = spessartine+clinochlore±hematite + H2O + O2 (1) sursassite + braunite + phengite + quartz = spessartine + phlogopite±hematite + H2O + O2 (2) and in braunite-free assemblages sursassite + Mn3+Fe –1 3+ [hematite, piemontite] + hematite + quartz = spessartine + clinochlore + H2O+O2 (3) Reactions (1) to (3) have positive P-T slopes. They are considered to account for the breakdown of sursassite and the formation of spessartine during prograde metamorphism of the piemontite quartzites and related rocks. P-T data from Andros and Evvia and geological data from few other occurrences reported suggest sursassite+ quartz±braunite to be stable at T<400–450° C over a considerable pressure interval at least up to 10 kbar. Theoretical phase relations among Mn3+-Mn2+-silicates in the pseudoquaternary system Al-Mn-Ca-Mg with excess quartz, H2O, and O2 indicate that low-grade assemblages containing sursassite (±braunite±pumpellyite±viridine±piemontite + quartz) are likely precursors of higher-grade assemblages including spessartine, Mg-chlorite, braunite, viridine, and piemontite reported from greenschist-, amphibolite-, and high-grade blueschist-facies rocks of appropriate composition.  相似文献   

12.
Eclogites from the Jæren nappe in the Caledonian orogenic belt of SW Norway contain aragonite, magnesite and dolomite in quartz‐rich layers. The carbonates comprise composite grains that occur interstitially between phases of the eclogite facies assemblage: garnet + omphacite + zoisite + clinozoisite + quartz + apatite + rutile ± dolomite ± kyanite ± phengite. Pressure and temperature conditions for the main eclogite stage are estimated to be 2.3–2.8 GPa and 585–655 °C. Published ultrahigh pressure (UHP) experiments on CaO‐, MgO‐ and CO2‐bearing systems have shown that equilibrium assemblages of aragonite and magnesite form as a result of dolomite breakdown at pressures >5 GPa. As a result, recognition of magnesite and aragonite in eclogite facies rocks has been used as an indicator for UHP conditions. However, petrological testing showed that the samples studied here have not experienced such conditions. Aragonite and magnesite show disequilibrium textures that indicate replacement of magnesite by aragonite. This process is inferred to have occurred via a coupled dissolution–precipitation reaction. The formation of aragonite is constrained to eclogite facies conditions, which implies that the studied rocks have experienced metasomatic, reactive fluid flow during their residence at high pressure (HP) conditions. During decompression, the bimineralic carbonate aggregates were overgrown by rims of dolomite, which partially reacted with aragonite to form Mg‐calcite. The well‐preserved carbonate assemblages and textures observed in the studied samples provide a detailed record of the reaction series that affected the rocks during and after their residence at P–T conditions near the coesite stability field. Recognition of the HP mechanism of magnesite replacement by aragonite provides new insight into metasomatic processes that occur in subduction zones and illustrates how fluids facilitate HP carbonate reactions that do not occur in dry systems at otherwise identical physiochemical conditions. This study documents that caution is warranted in interpreting aragonite‐magnesite associations in eclogite facies rocks as evidence for UHP metamorphic conditions.  相似文献   

13.
Early Archean (3.46 Ga) hydrothermally altered basaltic rocks exposed near Marble Bar, eastern Pilbara Craton, have been studied in order to reveal geological and geochemical natures of seafloor hydrothermal carbonatization and to estimate the CO2 flux sunk into the altered oceanic crust by the carbonatization. The basaltic rocks are divided into basalt and dolerite, and the basalt is further subdivided into type I, having original igneous rock textures, and type II, lacking these textures due to strong hydrothermal alteration. Primary clinopyroxene phenocrysts are preserved in some part of the dolerite samples, and the alteration mineral assemblage of dolerite (chlorite + epidote + albite + quartz ± actinolite) indicates that the alteration condition was typical greenschist facies. In other samples, all primary minerals were completely replaced by secondary minerals, and the alteration mineral assemblage of the type I and type II basalts (chlorite + K-mica + quartz + carbonate minerals ± albite) is characterized by the presence of K-mica and carbonate minerals and the absence of Ca-Al silicate minerals such as epidote and actinolite, suggesting the alteration condition of high CO2 fugacity. The difference of the alteration mineral assemblages between basalt and dolerite is probably attributed to the difference of water/rock ratio that, in turn, depends on their porosity.Carbonate minerals in the carbonatized basalt include calcite, ankerite, and siderite, but calcite is quite dominant. The δ13C values of the carbonate minerals are −0.3 ± 1.2‰ and mostly within the range of marine carbonate, indicating that the carbonate minerals were formed by seafloor hydrothermal alteration and that carbonate carbon in the altered basalt was derived from seawater. Whole-rock chemical composition of the basaltic rocks is essentially similar to that of modern mid-ocean ridge basalt (MORB) except for highly mobile elements such as K2O, Rb, Sr, and Ba. Compared to the least altered dolerite, all altered basalt samples are enriched in K2O, Rb, and Ba, and are depleted in Na2O, reflecting the presence of K-mica replacing primary plagioclase. In addition, noticeable CO2 enrichment is recognized in the basalt due to the ubiquitous presence of carbonate minerals, but there was essentially neither gain nor loss of CaO. This suggests that the CO2 in the hydrothermal fluid (seawater) was trapped by using Ca originally contained in the basalt. The CaO/CO2 ratios of the basalt are generally the same as that of pure calcite, indicating that Ca in the basalt was almost completely converted to calcite during the carbonatization, although Mg and Fe were mainly redistributed into noncarbonate minerals such as chlorite.The carbon flux into the Early Archean oceanic crust by the seafloor hydrothermal carbonatization is estimated to be 3.8 × 1013 mol/yr, based on the average carbon content of altered oceanic crust of 1.4 × 10-3 mol/g, the alteration depth of 500 m, and the spreading rate of 1.8 × 1011 cm2/yr. This flux is equivalent to or greater than the present-day total carbon flux. It is most likely that the seafloor hydrothermal carbonatization played an important role as a sink of atmospheric and oceanic CO2 in the Early Archean.  相似文献   

14.
Summary At the northeastern flank of Gebel Yelleq, northern Sinai, pure limestones of Upper Cretaceous age were subjected to a thermal overprint, caused by a c. 80m thick Tertiary olivine dolerite sill. Metasomatic supply of Si, Al, Fe, Mg and Ti was greater to the c. 7m wide upper than to the c. 25m wide lower thermal aureole. The greater width of the lower aureole is possibly due to a longer duration of the thermal overprint at this contact. Mineral assemblages in both aureoles are (from the contact outward):(i) clinopyroxene + garnet ± wollastonite + calcite(ii) garnet ± wollastonite + calcite;(iii) wollastonite + calcite.In places, late stage xenoblasts of apophyllite and witherite overgrow these assemblages. Garnets are grandites to melanites with Grs56–86Adr14–42Sch0–2Sps0–0.2Prp0 in the lower, and Grs29–94Adr5–64Sch0–12Sps0–0.2Prp0–1.7 in the upper aureole. Close to the upper contact, clinopyroxene is virtually pure diopside with X Mg = Mg/(Mg + Fe2+) = 0.97–1.0, whereas clinopyroxenes farther away from the upper contact and in the lower aureole have X Mg-values of 0.49 and 0.53, respectively.The minimum temperatures reached during contact metamorphism in the upper and lower aureole are defined by the lower stability limit of wollastonite. The temperatures are inferred with a calculated T-X(CO2) projection in the system CMASCH and are estimated at c. 290 °C and 380 °C for X(CO2) values of 0.05 and 0.25, respectively. A pressure of roughly 100 bar is estimated for the lower dolerite-limestone contact. As indicated by one-dimensional thermal modelling, a maximum temperature of 695 °C was attained at this contact, assuming a magma temperature of 1150 °C. Further modelling results indicate (i) wollastonite, which occurs first 13 m away from the lower contact, formed at a maximum temperature of c. 575 °C, (ii) there, wollastonite formation lasted for approximately 170 years and, (iii) at the outer rim of the lower aureole, the maximum temperature reached was 480 °C, and temperatures sufficient for wollastonite formation lasted for about 140 years.  相似文献   

15.
The stability of merwinite (Mw) and its equivalent assemblages, akermanite (Ak)+calcite (Cc), diopside (Di)+calcite, and wollastonite (Wo)+monticellite (Mc)+calcite was determined at T=500–900° C and P f=0.5–2.0 kbar under H2O–CO2 fluid conditions with X CO 2=0.5, 0.1, 0.05, and 0.02. Merwinite is stable at P f=0.5 kbar with T>700° C and X CO 2<0.1. At P f=2.0 kbar, the assemblage Di+Cc replaces merwinite at all T and X CO 2 conditions. At intermediate P f=1 kbar, the assemblage Ak+Cc is stable above 707° C and Wo+Mc+Cc is stable below 707° C. The univariant curve for the reaction Di+Cc=Wo+Mc+CO2 is almost parallel to the T axis and shifts to low P f with increasing X CO 2, with the assemblage Di+Cc on the high-P f side. The implications of the experimental results in regard to contact metamorphism of limestone are discussed using the aureole at Crestmore, California as an example.  相似文献   

16.
Coexisting garnet blueschist and eclogite from the Chinese South Tianshan high‐pressure (HP)–ultrahigh‐pressure (UHP) belt consist of similar mineral assemblages involving garnet, omphacite, glaucophane, epidote, phengite, rutile/sphene, quartz and hornblendic amphibole with or without paragonite. Eclogite assemblages generally contain omphacite >50 vol.% and a small amount of glaucophane (<5 vol.%), whereas blueschist assemblages have glaucophane over 30 vol.% with a small amount of omphacite which is even absent in the matrix. The coexisting blueschist and eclogite show dramatic differences in the bulk‐rock compositions with higher X(CaO) [=CaO/(CaO + MgO + FeOtotal + MnO + Na2O)] (0.33–0.48) and lower A/CNK [=Al2O3/(CaO + Na2O + K2O)] (0.35–0.56) in eclogite, but with lower X(CaO) (0.09–0.30) and higher A/CNK (0.65–1.28) in garnet blueschist. Garnet in both types of rocks has similar compositions and exhibits core–rim zoning with increasing grossular and pyrope contents. Petrographic observations and phase equilibria modelling with pseudosections calculated using thermocalc in the NCKMnFMASHO system for the coexisting garnet blueschist and eclogite samples suggest that the two rock types share similar P–T evolutional histories involving a decompression with heating from the Pmax to the Tmax stage and a post‐Tmax decompression with slightly cooling stage, and similar P–T conditions at the Tmax stage. The post‐Tmax decompression is responsible for lawsonite decomposition, which results in epidote growth, glaucophane increase and omphacite decrease in the blueschist, or in an overprinting of the eclogitic assemblage by a blueschist assemblage. Calculated P–X(CaO), P–A/CNK and P–X(CO2) pseudosections indicate that blueschist assemblages are favoured in rocks with lower X(CaO) (<0.28) and higher A/CNK (>0.75) or fluid composition with higher X(CO2) (>0.15), but eclogite assemblages preferentially occur in rocks with higher X(CaO) and lower A/CNK or fluid composition with lower X(CO2). Moreover, phase modelling suggests that the coexistence of blueschist and eclogite depends substantially on P–T conditions, which would commonly occur in medium temperatures of 500–590 °C under pressures of ~17–22 kbar. The modelling results are in good accordance with the measured bulk‐rock compositions and modelled temperature results of the coexisting garnet blueschist and eclogite from the South Tianshan HP–UHP belt.  相似文献   

17.
The regional distribution of metamorphic mineral assemblages in Mesozoic carbonate rocks of the Western Hohe Tauern allows the mapping of isograds based on the appearance of biotite+calcite and biotite+zoisite+calcite. The latter isograd corresponds approximately to the thermal maximum of the alpidic metamorphism in the central part of this area. An estimate of P, T, X fluid conditions can be obtained from phase relations among muscovite, biotite, chlorite, margarite, tremolite, zoisite, anorthite, quartz, calcite, and dolomite in the system K2O-CaO-MgO-Al2O3-SiO2-H2O-CO2 which approximates the composition of marls. Calculations based on various experimental and thermodynamic data have been made with emphasis on phase relations pertinent to a group of carbonate rocks with very low Fe and Na contents in non-opaque minerals. Significant and opposite deviations from the phase relations for stochiometric end member mineral compositions are due to the substitutions F-OH and Mg+Si-2Al. Consistency of observed and calculated phase relations is favoured by high F-contents. For the majority of carbonate rocks in the high metamorphic zone, maximum temperatures around 550° C, minimum pressures of 4–6 kb, and relatively low XCO2 values within the stability field of zoisite and of biotite+calcite+quartz are indicated.  相似文献   

18.
《Applied Geochemistry》1988,3(5):499-516
“Stratabound” disseminated pyritic Au ore bodies were produced by reactions between wall rocks and through-flowing fluids in Mesozoic epigenetic Au quartz vein systems in the Sierra Nevada metamorphic belt. Equilibrium relations among Fe-bearing carbonate and sulfide minerals were critical in determining which rock types were likely to host disseminated mineralization along portions of discordant veins. The compositions of metasomatic carbonates in hydrothermally altered wall rocks at Alleghany, California, U.S.A., were larely predetermined by the relative proportions of Fe, Mg and Ca in the unaltered wall rocks. Thus, coexisting solid solutions in the magnesite-siderite and dolomite-ankerite series from a variety of different wall rocks yield an empirical phase diagram for a large part of the Ca CO3MgCO3FeCO3 system at the temperature of metasomatism (325 ± 50°C). Because Fe,Mg-silicates were unstable in alteration zones adjacent to the veins, wall rock Fe was partitioned between carbonates and sulfides. Pyritization and disseminated Au mineralization occur in a variety of igneous and metasedimentary wall rocks in which the initial molar Fe/(Fe + Mg) ≧ 0.5. In altered wall rocks with initial molar Fe/(Fe + Mg) ≦ 0.5, Fe was incorporated almost entirely within Mg-rich carbonates (XFeCO3 ≦ 0.6 in magnesite-siderite solutions). It is proposed that the CO2-rich vein fluid responsible for the alteration and mineralization was partially buffered with respect to H2S/CO2/H2 ratios by equilibrium between pyrite and Mg0.4Fe0.6CO3 (+graphite?) as it traversed and altered intermediate volcanic and sedimentary rocks. This fluid then locally reacted with lower Fe/(Fe + Mg) rocks to form Fe-bearing dolomite + magnesite assemblages, and reacted with higher Fe/(Fe + Mg) rocks to form ankerite + pyrite assemblages. Gold precipitated from saturated solutions of bisulfide complexes partly in response to fluid desulfidation and reduction caused by the pyritization reactions. In terranes dominated by intermediate metavolcanic and metasedimentary rocks, favorable host rocks for this type of mineralization need not have high Fe contents, but do require high Fe/(Fe + Mg) ratios. They may include felsic volcanic and plutonic rocks, Fe-rich tholeiitic differentiates, banded Fe formations, and a variety of siliceous and argillaceous sedimentary rocks. Rocks which tend not to be heavily sulfidized because they have low initial Fe/(Fe + Mg) ratios include ultramafic and mafic igneous rocks, and some argillaceous sedimentary rocks. Exploration guidelines based on these principles may be useful elsewhere in the Sierra Nevada and in other comparable heterogeneous metamorphic terranes, if modified to reflect the dominant buffering rock types in a given fluid flow path. Carbonate-sulfide equilibria are capable of approximately buffering the carbonate-sulfide ratios of CO2-rich vein fluids (fCO2≧ 102.8 at 325°C, 200MPa or 2000 bar). The Alleghany fluid (fCO2 ≈ 103.2, or ∼ 10 mol % CO2) had a molar CO2/H2S ratio of approximately 103, assuming graphite saturation. At lower CO2 fugacities, Fe-bearing silicates entered the buffering assemblages. Carbonatization reactions could potentially de-sulfidize some wall rocks, releasing S (and associated metals?) to the fluid. This would be most likely to occur in pyrite-bearing mafic and ultramafic rocks and some argillites.  相似文献   

19.
The metamorphic paragenesis of cordierite in pelitic rocks   总被引：2，自引：0，他引：2  
A petrogenetic grid is constructed for mineral assemblages occurring in metapelitic rocks, particularly those involved in the paragenesis of cordierite. The most useful assemblages for estimating pressures and temperatures are staurolite-cordierite, cordierite-biotite-Al2SiO5 and cordierite-hypersthene. Cordierite is stable with kyanite, sillimanite or andalusite. At high pressures cordierite is Mg-rich so that pelitic rocks typically do not contain the phase. Cordierite is stable at temperatures less than 500° C but does not commonly appear in metapelitic rocks until the garnet-chlorite, chlorite-staurolite or chlorite-Al2SiO5 tie-lines are broken. At high metamorphic grades, the assemblage garnet-hypersthene-cordierite indicates relatively low pressures, and the assemblage hypersthene-cordierite-sillimanite relatively high pressures. It is clear however, that the absence of cordierite is of little use in characterizing a metamorphic facies unless an alternate mineral assemblage can be shown to be more stable.  相似文献   

20.
The pumpellyite–actinolite facies proposed by Hashimoto is defined by the common occurrence of the pumpellyite–actinolite assemblage in basic schists. It can help characterize the paragenesis of basic and intermediate bulk compositions, which are common constituents of various low-grade metamorphic areas. The dataset of mutually consistent thermodynamic properties of minerals gives a positive slope for the boundary between the pumpellyite–actinolite and prehnite–pumpellyite facies in P–T space. In the Sanbagawa belt in Japan, the mineral parageneses of hematite-bearing and -free basic schists, as well as pelitic schists have been well documented. The higher temperature limit of this facies is defined by the disappearance of the pumpellyite+epidote+actinolite+chlorite assemblage in hematite-free basic schists with XFe3+ of epidote around 0.20–0.25 and the appearance of epidote+actinolite+chlorite assemblage with XEpFe3+≤0.20. In hematite-bearing basic schists, there is a continuous change of paragenesis to higher grade, epidote–glaucophane or epidote–blueschist facies. In pelitic schists, the albite+lawsonite+chlorite assemblage does occur but only rarely, and its assemblage cannot be used to determine the regional thermal structure. The lower temperature equivalence of the pumpellyite–actinolite assemblage is not observed in the field. The Mikabu Greenstone complex and the northern margin of the Chichibu complex, which are located to the south of the Sanbagawa belt, are characterized by clinopyroxene+chlorite or lawsonite+actinolite assemblages, which are lower temperature assemblages than the pumpellyite+actinolite assemblage. These three metamorphic complexes belong to the same subduction-metamorphic complex. The pumpellyite–actinolite facies or subfacies can be useful to help reveal the field thermal structure of metamorphic complexes  相似文献   

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