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1.
Abstract Mineral equilibria in the system CaO–MgO–Al2O3–SiO2–H2O provide a basis for mapping of four reaction isograds and one bathograd in the low-pressure transition from subgreenschist to greenschist facies. Most of the Matachewan area of the Abitibi greenstone belt is in the lower-pressure bathozone, as indicated by the widespread occurrences of the subassemblage Prh–Chl. The higher-pressure bathozone is indicated by two occurrences of Pmp–Act–Ep–Qtz, but in these samples the bathograd is displaced to anomalously low pressure by the high Fe content of the coexisting minerals. This illustrates the need to analyse coexisting minerals, calculate activities of end-member species, and compute P–T curves for individual samples before interpreting the isograd/bathograd pattern. Petrographic and microprobe analysis indicates that great care must be taken in the selection of ‘equilibrium’ assemblages. Pyroxene phenocrysts in one sample are replaced by the assemblage Pmp–Act–Ep–Chl–Qtz, whereas Prh–Act–Ep–Chl–Qtz occurs in the groundmass. Compositional variation may be more cryptic, as in a sample of metabasaltic hyaloclastite that contains two spatially distinct ‘univariant’ assemblages, Prh–Pmp–Ep–Chl–Qtz and Prh–Act–Ep–Chl–Qtz, within the devitrified matrix. Whereas chlorite compositions are similar in both assemblages, prehnite and epidote in the latter assemblage are significantly richer in Fe and poorer in Al. Accordingly, the rock is interpreted to contain two distinct ‘univariant’ assemblages, rather than one ‘invariant’ assemblage (Prh–Pmp–Act–Ep–Chl–Qtz). The displaced ‘univariant’ curves for this sample intersect at 2.2 kbar and 250°C. Taking account of all thermobarometric implications, the low-grade limit of the greenschist facies is at 250–270°C and 2–2.5 kbar, corresponding to depths of 7–8 km. Comparison of apparent P–T conditions on both sides of the Larder Lake – Cadillac break, a regional CO2-metasomatized fault zone that is spatially associated with many Archaean gold deposits, provides an upper limit of not more than c. 1 km for post-metamorphic south-side-up, dip-slip displacement.  相似文献   

2.
Fluid infiltration into retrograde granulites of the Southern Marginal Zone(Limpopo high grade terrain)is exemplified by hydration reactions.shear zone hosted metasomatism,and lode gold mineralisation.Hydration reactions include the breakdown of cordierite and orthopyroxene to gedrite kyanite,and anthophyllite,respectively.Metamorphic petrology,fluid inclusions,and field data indicate that a low H_2O-activity carbon-saturated CO_2-rich and a saline aqueous fluid infiltrated the Southern Marginal Zone during exhumation.The formation of anthophyllite after orthopyroxene eslablished a regional retrograde anthophyllite-in isograd and occurred at P-T conditions of- 6 kbar and 610 C,which fixes the minimum mole fraction of II.0 in the CO_2-rich fluid phase at- 0.1.The maximum H_2O mole fraction is hxed by the lower temperature limit(~800℃) for partial melting at ~0.3.C-O-H fluid calculations show that the CO_2-rich fluid had an oxygen fugacity that was 0.6 log10 units higher than that of the fayalite-magnetitequartz buffer and that the CO_2/(CO_2+CH_4) mole ratio of this fluid was 1.The presence of dominantly relatively low density CO_2-rich fluid inclusions in the hydrated granulites indicates that the fluid pressure was less than the lithostatic pressure.This can be explained by strike slip faulting and/or an increase of the rock permeability caused by hydration reactions.  相似文献   

3.
ABSTRACT The metasedimentary sequence of the Deep Freeze Range (northern Victoria Land, Antarctica) experienced high-T/low-F metamorphism during the Cambro-Ordovician Ross orogeny. The reaction Bt + Sil + Qtz = Grt + Crd + Kfs + melt was responsible for the formation of migmatites. Peak conditions were c. 700–750° C, c. 3.5–5 kbar and xH2Oc. 0.5). Distribution of fluid inclusions is controlled by host rock type: (1) CO2-H2O fluid inclusions occur only in graphite-free leucosomes; (2) CO2–CH4± H2O fluid inclusions are the most common type in leucosomes, and in graphite-bearing mesosomes and gneiss; and (3) CO2–N2–CH4 fluid inclusions are observed only in the gneiss, and subordinately in mesosomes. CO2–H2O mixtures (41% CO2, 58% H2O, 1% Nad mol.%) are interpreted as remnants of a synmig-matization fluid; their composition and density are compatible P–T–aH2O conditions of migmatization (c. 750° C, c. 4 kbar, xH2Oc. 0.5). CO2-H2O fluid in graphite-free leucosomes cannot originate via partial melting of graphite-bearing mesosomes in a closed system; this would have produced a mixed CO2–CH4 fluid in the leucosomes by a reaction such as Bt + Sil + Qtz + C ± H2O = Grt + Crd + Kfs + L + CO2+ CH4. We conclude that an externally derived oxidizing CO2-H2O fluid was present in the middle crust and initiated anatexis. High-density CO2-rich fluid with traces of CH4 characterizes the retrograde evolution of these rocks at high temperatures and support isobaric cooling (P–T anticlockwise path). In unmigmatized gneiss, mixed CO2–N2–CH4 fluid yields isochores compatible with peak metamorphic conditions (c. 700–750° C, c. 4–4.5 kbar); they may represent a peak metamorphic fluid that pre-dated the migmatization.  相似文献   

4.
Metapelites, migmatites and granites from the c. 2 Ga Mahalapye Complex have been studied for determining the P–T–fluid influence on mineral assemblages and local equilibrium compositions in the rocks from the extreme southwestern part of the Central Zone of the Limpopo high‐grade terrane in Botswana. It was found that fluid infiltration played a leading role in the formation of the rocks. This conclusion is based on both well‐developed textures inferred to record metasomatic reactions, such as Bt ? And + Qtz + (K2O) and Bt ± Qtz ? Sil + Kfs + Ms ± Pl, and zonation of Ms | Bt + Qtz | And + Qtz and Grt | Crd | Pl | Kfs + Qtz reflecting a perfect mobility (Korzhinskii terminology) of some chemical components. The conclusion is also supported by the results of a fluid inclusion study. CO2 and H2O ( = 0.6) are the major components of the fluid. The fluid has been trapped synchronously along the retrograde P–T path. The P–T path was derived using mineral thermobarometry and a combination of mineral thermometry and fluid inclusion density data. The Mahalapye Complex experienced low‐pressure granulite facies metamorphism with a retrograde evolution from 770 °C and 5.5 kbar to 560 °C and 2 kbar, presumably at c. 2 Ga.  相似文献   

5.
The Smartville Complex is a late Jurassic, rifted volcanic arc in the northern Sierra Nevada, California. Near Auburn, California, it consists of a lower volcanic unit, dominated by basaltic flows, and an upper volcanic unit of andesitic volcaniclastic rocks, both of which have been intruded by dykes and irregular bodies of diabase. These rocks contain relict igneous minerals, and the metamorphic minerals albite, chlorite, quartz, pumpellyite, prehnite, epidote, amphibole, titanite, garnet, biotite, K-feldspar, white mica, calcite, and sulphide and oxide minerals.
Prehnite–pumpellyite (PrP), prehnite–actinolite (PrA), and greenschist (GS) zones have been identified. The pumpellyite-out isograd separates the PrP and PrA zones, and the prehnite-out isograd separates the PrA and GS zones. The minerals Ab + Qtz + Mt + Tn are common to most assemblages in all three zones. The MgO/(MgO + FeO) ratio of the effective bulk composition has an important and systematic effect on the observed mineral assemblages in the PrP zone. Prehnite-bearing assemblages contain the additional minerals, Pmp + Amp + Ep + Chl in MgO-rich rocks, and either Pmp + Ep + Chl or Amp + Ep + Chl in less magnesian rocks. Subcalcic to calcic amphibole is common in the PrP zone. The mineral assemblage Prh + Act + Ep + Chl, without Pmp, characterizes the PrA zone, and the mineral assemblage Act + Ep + Chl, without Prh or Pmp, characterizes the GS zone. The disappearance of pumpellyite and prehnite occurred by continuous reactions.
The sequence of mineral assemblages was produced by burial metamorphism at P–T conditions of 300° 50°C at approximately 2.5 ± 0.5 kbar. During metamorphism, the composition of the fluid phase was nearly 100% H2O and the oxygen fugacity was between the hematite–magnetite and quartz–fayalite–magnetite buffers.  相似文献   

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

7.
Contact metamorphism of siliceous dolomite in the southern partof the metamorphic aureole of the Alta stock (Utah, USA) producedthe prograde isograd sequence: talc (Tc), tremolite (Tr), forsterite(Fo), and periclase (Per). Calcite (Cc)–dolomite (Do)geothermometry and phase equilibria define a general progradeT–X(CO2) path of decreasing X(CO2) with rising temperaturefor the dolomite. High-variance assemblages typify the aureole.Per + Cc and Fo + Cc + Do characterize the inner aureole (Perand Fo zones), and Tr + Do + Cc and Tc + Do + Cc are widespreadin the outer aureole (Tr and Tc zones). Low-variance assemblagesare rare and the thickness of reaction zones (coexisting reactantand product minerals) at the isogradic reaction fronts are narrow(tens of metres or less). The mineral assemblages, calculatedprogress of isograd reactions, and the prograde T–X(CO2)path all indicate that massive dolomite was infiltrated by significantfluxes of water-rich fluids during prograde metamorphism, andthat the fluid flow was down-temperature and laterally awayfrom the igneous contact. Fluid infiltration continued throughat least the initial retrograde cooling of the periclase zone.Down-T fluid flow is also consistent with the results of Cc–Dogeothermometry and patterns of 18O depletion in this area. Theclose spatial association of reacted and unreacted chert nodulesin both the tremolite and talc zones plus the formation of tremoliteby two reactions indicate that the outer aureole varied in X(CO2),and imply that fluid flow in the outer aureole was heterogeneous.The occurrence of dolomite-rich and periclase (brucite)-absent,high-  相似文献   

8.
In the inner aureole of the Bufa del Diente alkali syenite (north-east Mexico), thin calcareous argillite bands horizontally embedded in impure marbles acted as contact-metamorphic aquifers for hypersaline brines of magmatic origin. Thick-bedded marbles were largely impervious. From 180 m up to the intrusion contact, argillites were completely decarbonated, resulting in melilite + wollastonite + phlogopite + perovskite-bearing parageneses. In marbles, this assemblage is confined to a narrow 7-12-m-wide infiltration zone adjacent to the contact. Up to this distance, calcite + wollastonite + diopside + alkali feldspar + titanite was stable, indicating that the fluid evolution in these marbles was internally buffered. Brine infiltration from the metaargillite aquifer into the marbles occurred perpendicular to the marble-metaargillite boundaries and was confined to a zone 4-6 cm wide above the boundaries. This is documented by the three reactions Cc + Di = Mel + CO2, (1) Cc + Kfs + Di + H2O = Phl + Wo + CO2, (2) Cc + Ttn = Prv + Wo + CO2, (3) Melilites (Ak32-45Gh13-32Sm32-40 to Ak52-72Gh0-1Sm28-48) occur as rims around diopsides and become continuously thicker towards the metaargillite beds. Fluid inclusion observations suggest that the infiltrating brine was hypersaline (NaCl + KClcq～ 65 wt%) and that the reactions took place at the water-rich side of the H2O-CO2-salts immiscibility field at about 600d? C (2, 3) and 660 to 680d? C (1) at P～ 1200 bar and Xco2～ 0.02. Mass balance calculations show that the amount of brine infiltrated from the aquifer into the marble was very low and decreased continuously with increasing distance from the boundary. The maximum width of brine infiltration was about 6 cm. This confirms that brine flow was largely parallel to the aquifer, not perpendicular to it. The CO2 produced by the decarbonation reactions probably escaped as an immiscible low-density H2O-CO2 fluid of Xco2≤ 0.5 into overlying marble via grain-edge flow. The metaargillite-marble boundary acted as a semipermeable membrane 6 cm in thickness keeping back the brine in the aquifer and losing the in-situ produced low-density CO2-rich fluid.  相似文献   

9.
Felsic to mafic granulite xenoliths from late Neogene basalt pyroclastics in four localities of the western Pannonian Basin (Beistein, Kapfenstein, Szigliget and Káptalantóti (Sabar-hegy) were studied to find out their metamorphic and fluid history. The characteristic mineral assemblage of the granulites consists of Pl + Opx + Qtz ± Cpx ± Bt ± Grt ± Kfs. Based on abundant magmatic relic microstructural domains occurring in these rocks, the potential precursors might have been predominantly felsic igneous or high to ultrahigh temperature rocks. Ternary feldspar thermometry provides a rough estimate of temperatures of about 920–1070 °C. The first fluid invasion event, which is linked with this early high to ultrahigh temperature stage is characterised by primary pure CO2 inclusions in apatite and zircon. The densest primary CO2 inclusions indicate 0.52–0.64 GPa pressure at the estimated temperature range of crystallization. According to mineral equilibria and geothermobarometry, the high to ultrahigh temperature rock cooled and crystallized to granulite of predominantly felsic composition at about 750–870 °C and 0.50–0.75 GPa in the middle crust, between 20 and 29 km depths. The second fluid invasion event is recorded by primary CO2-rich fluid inclusions hosted in the granulitic mineral assemblage (plagioclase, quartz and orthopyroxene). In addition to CO2, Raman spectroscopy revealed the presence of minor N2, H2S, CO and H2O in these inclusions. Partial melting of biotite-bearing assemblages could be connected to the next fluid invasion shown by secondary CO2-rich fluids recorded along with healed fractures in plagioclase, clinopyroxene and orthopyroxene. This event could have happened at depths similar to the previous ones. The final step in the granulite evolution was the sampling in the middle crust and transportation to the surface in form of xenoliths by mafic melt. This event generated temperature increase and pressure decrease and thus, limited melting of the xenoliths. The youngest fluid inclusion generation, observed mostly in healed fractures of felsic minerals, could be associated with this event.  相似文献   

10.
Synorogenic veins from the Proterozoic Eastern Mount Isa Fold Belt contain three different types of fluid inclusions: CO2-rich, aqueous two-phase and rare multiphase. Inclusions of CO2 without a visible H2O phase are particularly common. The close association of CO2-rich inclusions with aqueous two-phase, and possibly multiphase inclusions suggests that phase separation of low- to -moderate salinity CO2-rich hydrothermal fluids led to the selective entrapment of the CO2. Microthermometric results indicate that CO2-rich inclusions homogenize between –15.5 and +29.9 °C which corresponds to densities of 0.99 to 0.60 g.cm−3. The homogenization temperatures of the associated aqueous two-phase inclusions are 127–397 °C, with salinities of 0.5 to 18.1 wt.% NaCl equivalent. The rarely observed multiphase inclusions homogenize between 250 and 350 °C, and have salinities ranging from 34.6 to 41.5 wt.% NaCl equivalent. Evidence used to support the presence of fluid immiscibility in this study is mainly derived from observations of coexisting H2O-rich and CO2-rich inclusions in groups and along the same trail. In addition, these two presumably unmixed fluids are also found on adjacent fractures where monophase CO2-rich inclusions are closely related to H2O-rich inclusions. Similar CO2-rich inclusions are widespread in mineral deposits in this region, which are simply metal-enriched synorogenic veins. Therefore, we argue that fluid immiscibility caused volatile species such as CO2 and H2S to be lost from liquid, thus triggering ore deposition by increasing the fluid pH and decreasing the availability of complexing ligands. Received: 28 April 1997 / Accepted: 4 January 1999  相似文献   

11.
Omphacite and garnet coronas around amphibole occur in amphibolites in the Hong'an area, western Dabie Mountains, China. These amphibolites consist of an epidote–amphibolite facies assemblage of amphibole, garnet, albite, clinozoisite, paragonite, ilmenite and quartz, which is incompletely overprinted by an eclogite facies assemblage of garnet, omphacite and rutile. Coronas around amphibole can be divided into three types: an omphacite corona; a garnet–omphacite–rutile corona; and, a garnet–omphacite corona with less rutile. Chemographic analysis for local reaction domains in combination with petrographical observations show that reactions Amp + Ab + Pg = Omp +Czo + Qtz + H2O, and Amp + Ab = Omp ± Czo + Qtz + H2O may lead to the development of omphacite coronas. The garnet–omphacite–rutile corona was formed from the reaction Amp + Ab + Czo + Ilm ± Qtz = Omp + Grt + Rt + H2O. In garnet–omphacite coronas, the garnet corona grew during an early stage of epidote amphibolite facies metamorphism, whereas omphacite probably formed by the reactions forming the omphacite corona during the eclogite facies stage. It is estimated that these reactions occurred at 0.8–1.4 GPa and 480–610 °C using the garnet–clinopyroxene thermometer and omphacite barometer in the presence of albite.  相似文献   

12.
Non-aqueous CO2 and CO2-rich fluid inclusions are found in the vein quartz hosting mesothermal gold-sulphide mineralization at Bin Yauri, northwestern Nigeria. Although mineralizing fluids responsible for gold mineralization are thought to be CO2-rich, the occurrence of predominantly pure to nearly pure CO2 inclusions is nevertheless unusual for a hydrothermal fluid system. Many studies of similar CO2-rich fluid inclusions, mainly in metamorphic rocks, proposed preferential loss (leakage) of H2O from H2O-CO2 inclusions after entrapment. In this study however, it is proposed that phase separation (fluid immiscibility) of low salinity CO2-rich hydrothermal fluids during deposition of the gold mineralization led to the loss of the H2O phase and selective entrapment of the CO2. The loss of H2O to the wallrocks resulted in increasing oxidizing effects. There is evidence to suggest that the original CO2-rich fluid was intrinsically oxidized, or perhaps in equilibrium with oxidizing conditions in the source rocks. The source of the implicated fluid is thought to be subducted metasediments, subjected to dehydration and devolatilization reactions along a transcurrent Anka fault/shear system, which has been described as a Pan-African (450–750 Ma) crustal suture.  相似文献   

13.
Thermodynamic and phase equilibrium data for scapolite have been used to calculate CO2 activities (aCO2) and to evaluate the presence or absence of a fluid phase in high-grade scapolite bearing meta-anorthosite, granulites, calc-silicates, and mafix xenoliths. The assemblage scapolite-plagioclase-garnet±quartz may be used to calculate or limit aCO2 by the reaction Meionite+Quartz = Grossular+Anorthite+CO2. Granulites from four high-grade terranes (Grenville Province, Canada; Sargut Belt, India; Furua Complex, Tanzania; Bergen Arcs, Norway) yield aCO2=0.4-1, with most >0.7. For scapolite-bearing granulites from the Furua Complex, in which aCO2≥0.9, calculated H2O activities (aH2O) based on phlogopite dehydration equilibria are uniformly low (0.1–0.2). The aCO2 calculated for meta-anorthosite from the Grenville Province, Ontario, ranges from 0.2 to 0.8. For Grenville meta-anorthosite also containing epidote, the aH2O calculated from clinozoisite dehydration ranges from 0.2 to 0.6. Calc-silicates from the Grenville, Sargur, and Furua terranes mostly yield aCO2< 0.5. The presence of calcite and/or wollastonite provides additional evidence for the low aCO2 in calc-silicates. Samples from six xenolith localities (Lashaine, Tanzania; Eifel, W. Germany; Lesotho; Delegate, Gloucester, and Hill 32, Australia) yield a wide range of aCO2 (0.1 to >1). The calculated fluid activities are consistent with metamorphism (1) in the presence of a mixed CO2−H2O fluid phase in which CO2 is the dominant fluid species but other C−O−H−S species are minor, (2) in the absence of a bulk fluid phase (“fluid-absent metamorphism”), or (3) in the presence of a fluid-bearing melt phase. The results for many granulites and Grenville meta-anorthosite are consistent with the presence of a CO2-rich, mixed CO2−H2O fluid phase. In contrast the relatively restricted and low values of aCO2 for calc-silicates require an H2O-rich fluid or absence of a fluid phase during metamorphism. The range of values for xenoliths are most consistent with absence of a fluid phase. The primary implication of these results is that a CO2-rich fluid accounts for the reduced aH2O in scapolite-bearing granulites. However, scapolite may be stable with a wide range of fluid compositions or in the absence of a fluid phase, and the presence of scapolite is not a priori evidence of a CO2-rich fluid phase. In addition, close association of scapolite-free mafic granulites with scapolite-bearing granulites having identical mineral compositions in the Furua Complex, and the absence of scapolite from most granulite terranes implies that a CO2-rich fluid phase is not pervasive on an outcrop scale or common to all granulite terranes. Contribution No. 474 from the Mineralogical Laboratory, University of Michigan  相似文献   

14.
胶北莱西古元古代的高压基性麻粒岩和钙硅酸盐岩的基本矿物组合分别为以铁铝榴石为主的石榴石-普通辉石-铁紫苏辉石和钙铝榴石-黝帘石-葡萄石-钠长石.矿物岩石学研究表明钙硅酸盐岩是由含石榴石高压基性麻粒岩经退变质和钙质交代作用形成.南山口高压基性麻粒岩记录了麻粒岩相变质作用前、麻粒岩相变质作用、退变质和钙硅酸盐岩化共同作用以及完全钙硅酸盐岩化的四个阶段的地质作用,其矿物组合分别为Cpx+ Pl+ Qtz(M1),Grt+ Cpx+ Rt+ Qtz(M2),Cpx+Pl+ Opx+ Ilm+ Mgt+ Ep(M3)和Grs+ Zo+ Prh+ Ab+ Cal(M4).微量元素研究表明,高压基性麻粒岩中大离子亲石元素Ba、Rb、K、Rb、Th富集,而高场强元素Nb、Zr、Ti、Y亏损,具有轻稀土富集的右倾型稀土配分曲线.稀土元素和微量元素配分图解显示了岛孤拉斑玄武岩的特征.主元素、微量元素的构造判别图解进一步分析表明高压基性麻粒岩及其钙硅酸盐岩的原岩形成于大陆边缘的岛弧环境.综合高压基性麻粒岩岩石学、元素地球化学特征认为,莱西高压基性麻粒岩的原岩是拉斑玄武岩质岩石,可能是形成于孤后扩张背景下基性的侵入岩或喷出岩.岩石形成以后,在胶-辽-吉带碰撞闭合过程中,经历了麻粒岩相变质作用,又在后来的抬升过程中经历退变质和钙硅酸盐岩化作用.  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.
Geothermometry and geobarometry of plagioclase-hornblende bearing assemblages   总被引：10，自引：0，他引：10  
The reaction Hb+Zo(Ep)+H2O+CO2⇌Pl+ Chl+Cc+Q was studied under hydrothermal conditions at P total=2, 4, 6 and 8 kb at . The continious transition from tremolite (actinolite) to Al-rich hornblende was fixed along the equilibrium curve of the reaction, providing a complete solid solution in the calcic amphibole series. A dependence of Al content in Ca-amphiboles and coexisting plagioclases on PT-conditions of their crystallization, determined for a wide range of temperature (450–650° C) and pressure (2–8 kb), has been used for construction of the experimental geothermobarometer. This may be employed to deduce temperature and pressure conditions of metamorphism of the albite-epidote-amphibolite and the amphibolite facies metabasites, including zoisite (or epidote)-bearing assemblages. An application of the Hb-Pl geothermobarometer is illustrated on the Patom Highland amphibolites and also on the well-known mafic schists of Vermont.  相似文献   

17.
Four assemblages from calcic pelitic schists from South Strafford,Vermont, have been studied in detail to determine the relationshipbetween reaction history and compositional zoning of minerals.The lowest-grade assemblage is garnet + biotite + chlorite +plagioclase + epidote + quartz + muscovite + graphite + fluid.Along a path of isobaric heating, the net reaction is Chl +Ms + Ep + Gr = Grt + Bt + Pl + fluid. Garnet grows with decreasingFe/(Fe + Mg) and XSpa, (from 0•2 to 0•05), XGra staysnearly constant between 0•20 and 0•25, and plagioclasegrows with XAn increasing from peristerite to 0•2–0•5. The subsequent evolution depends on whether chlorite or epidotereacts out first. If chlorite is removed from the assemblagefirst, the net reaction along an isobaric heating path becomesGrt + Ms + Ep + Qtz + Gr = Bt + Pl + fluid. XAn of plagioclaseincreases to 0•20–0•70, depending on the bulk-rockcomposition and changes in pressure and temperature. If epidoteis removed first, the assemblage becomes a simple pelite andthe net reaction becomes Chl + Pl + Ms + Qtz = Grt + Bt + H2O.Plagioclase is consumed to provide Ca for growing garnet, andXAn, Fe/(Fe + Mg) of garnet, XGra, and XSpa all decrease. Afterboth chlorite and epidote are removed, continued heating upto the metamorphic peak of {small tilde}600C produces littleprogress of the reaction Grt + Ms = Bt + Pl; and XAn increases. The four assemblages have been numerically modeled using theGibbs method starting with measured compositions. The modelssuccessfully predict the observed compositional zoning and trendsof mineral growth and consumption along the computed P–Tpaths. The models also predict the compositional mineral zoningthat would have resulted from other P–T paths. * Present address: Department of Geology, University of Alabama, Tuscaloosa, Alabama 35487  相似文献   

18.
Abstract Fluid evolution paths in the COHN system can be calculated for metamorphic rocks if there are relevant data regarding the mineral assemblages present, and regarding the oxidation and nitrodation states throughout the entire P-T loop. The compositions of fluid inclusions observed in granulitic rocks from Rogaland (south-west Norway) are compared with theoretical fluid compositions and molar volumes. The fluid parameters are calculated using a P-T path based on mineral assemblages, which are represented by rocks within the pigeonite-in isograd and by rocks near the orthopyroxene-in isograd surrounding an intrusive anorthosite massif. The oxygen and nitrogen fugacities are assumed to be buffered by the coexisting Fe-Ti oxides and Cr-carlsbergite, respectively. Many features of the natural fluid inclusions, including (1) the occurrence of CO2-N2-rich graphite-absent fluid inclusions near peak M2 metamorphic conditions (927° C and 400 MPa), (2) the non-existence of intermediate ternary CO2-CH4-N2 compositions and (3) the low-molar-volume CO2-rich fluid inclusions (36–42 cm3 mol?1), are reproduced in the calculated fluid system. The observed CO2-CH4-rich inclusions with minor N2 (5 mol%) should also include a large proportion of H2O according to the calculations. The absence of H2O from these natural high-molar-volume CO2-CH4-rich inclusions and the occurrence of natural CH4-N2-rich inclusions are both assumed to result from preferential leakage of H2O. This has been previously experimentally demonstrated for H2O-CO2-rich fluid inclusions, and has also been theoretically predicted. Fluid-deficient conditions may explain the relatively high molar volumes, but cannot be used to explain the occurrence of CH4-N2-rich inclusions and the absence of H2O.  相似文献   

19.
An amphibole-bearing gneiss from the Seward Peninsula, Alaska,underwent local dehydration to two-pyroxene gneiss. Dehydrationwas driven isothermally and isobarically, close to the metamorphicmaximum, by a small amount of CO2-rich fluid evolved from anunderlying impure marble layer. Stable isotope evidence indicatesthat the CO2 diffused 85 cm into the gneiss through a stationarypore fluid that was seldom fully connected. This created a gradientin H2O activity from 0.20 to 0.24 within the two-pyroxene alterationzone. Whole-rock analyses and mineral mass balances suggestthat, apart from loss of H2O, the change proceeded isochemically,a conclusion that differs from some of the more recent detailedchemical studies of outcrop-scale charnockitic alteration. Hornblendereacted out according to the reaction Hbl+1.86 Qtz=1.26 Cpx+1.36Opx+0.96 An65+0.29 Kfs+0.23 Ilm+H2O. Biotite was largely conserved.Clinopyroxene, orthopyroxene, and new-formed plagioclase occurin relatively fine-grained granular aggregates. New-formed K-feldsparoccurs as replacement antiperthite. It is argued that the reactiondid not involve the production of anatectic melt. We suggestthat CO2-induced dehydration in its simplest form is isochemical.We further suggest that the sequence of disappearance of biotiteand hornblende in prograde granulite terranes may be indicativeof the process of simple dehydration (at low aH2O) or vapor-absentdehydration melting (at higher T and aH2O). Our observationsmay be helpful in interpreting cases where the evidence forintroduced CO2 is more ambiguous.  相似文献   

20.
Beryl crystals from the stockscheider pegmatite in the apical portion of the Li-F granite of the Orlovka Massif in the Khangilay complex, a tantalum deposit, contain an assemblage of melt and fluid inclusions containing two different and mutually immiscible silicate melts, plus an aqueous CO2-rich supercritical fluid. Pure H2O and CO2 inclusions are subordinate. Using the terminology of Thomas R, Webster JD, Heinrich W. Contrib Mineral Petrol 139:394–401 (2000) the melt inclusions can be classified as (i) water-poor type-A and (ii) water-rich type-B inclusions. Generally the primary trapped melt droplets have crystallized to several different mineral phases plus a vapor bubble. However, type-B melt inclusions which are not crystallized also occur, and at room temperature they contain four different phases: a silicate glass, a water-rich solution, and liquid and gaseous CO2. The primary fluid inclusions represent an aqueous CO2-rich supercritical fluid which contained elemental sulfur. Such fluids are extremely corrosive and reactive and were supersaturated with respect to Ta and Zn. From the phase compositions and relations we can show that the primary mineral-forming, volatile-rich melt had an extremely low density and viscosity and that melt-melt-fluid immiscibility was characteristic during the crystallization of beryl. The coexistence of different primary inclusion types in single growth zones underlines the existence of at least three mutually immiscible phases in the melt in which the large beryl crystals formed. Moreover, we show that the inclusions do not represent an anomalous boundary layer.  相似文献   

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