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1.
Charnockitization of mafic Opx-Cpx-Grt-Hbl-Bt-Pl ± Qtz granulites and Hbl-Opx-Bt hornblendites was studied in the southeastern part of the Lapland Granulite Belt. The evolutionary trends of the whole-rock compositions and mineral assemblages indicate that the rocks were affected by Na-K-Si-H2O-CO2-Cl brines, which came from outside, alkalinized and debasified the granulites, introduced Na, K, and Si into them, and depleted them in Mg, Fe, and Ca prior to the onset of charnockite melting; the latter began in the granulites only in their most extensively debasified domains. In the course of alkaline metasomatism, pyroxene were replaced by secondary hornblende and biotite with high Ti concentrations, analogous to those in the unaltered granulites. This suggests that the pre-charnockite amphibolization and biotitization were induced not by a temperature decrease but by the effect of Na- and K-bearing fluid during the metamorphic culmination. The metasomatically altered granulites, which were transformed into leucocratic disintegrated amphibolite skialiths, were gradually resorbed and dissolved in the charnockite melt, whose bulk composition corresponded to low-alkaline granites and tonalites. Hence, no contamination took place, and the excess Mg, Fe, and Ca amounts with respect to the eutectic composition were removed from the reaction zone. Variation diagrams indicate that the whole-rock composition of the granulites is gradually shifted toward the composition of charnockitoids. In certain instances, however, melanocratic Hbl-Grt-Opx-Cpx-Pl rims were formed along the granulite-charnockite interface, with the bulk composition of these fringes richer in Mg, Fe, and Ca than that of the ambient granulites. The reason for this was the sporadic redeposition of Mg, Fe, and Ca, which were mobilized from during charnbockitization and redeposited immediately in the reaction zone. In addition, rocks around the charnockite veins bear autonomous melanocratic Grt-Opx-Cpx-Hbl ± Mag ± Ilm ± Scp ± Pl ± Qtz veins whose mineral assemblages and bulk composition are close to those of the melanocratic rims around charnockitoids. The veins were formed via the transportation of Mg, Fe, and Ca for long distances outside the charnockitization zones. TWQ thermobarometric calculations indicate that the pre-charnockite alkaline metasomatism and debasification (amphibolization, biotitization, and feldspathization), anatectic formation of charnockite migma or magma, and the development of the melanocratic veins took place at the peak of the high-pressure granulite metamorphism at the same P-T parameters: approximately 800°C and 9–9.5 kbar. The calculated composition of the charnockitizing fluids suggests that they were homogeneous brines with $ X_{H_2 O} = 0.45 $ X_{H_2 O} = 0.45 , $ X_{CO_2 } = 0.10 $ X_{CO_2 } = 0.10 , X NaCl = 0.30, and X KCl = 0.15.  相似文献   

2.
Arrested charnockite formation at Kottavattam, southern India   总被引：7，自引：0，他引：7  
Abstract At Kottavattam, southern Kerala (India), late Proterozoic homogeneous leptynitic garnet–biotite gneisses of granitic composition have been transformed on a decimetric scale into coarse-grained massive charnockite sensu stricto along a set of conjugate fractures transecting the gneissic foliation. Charnockitization post-dates the polyphase deformation, regional high-grade metamorphism and anatexis, and evidently occurred at a late stage of the Pan-African tectonothermal history. Geothermobarometric and fluid inclusion data document textural and chemical equilibration of the gneiss and charnockite assemblages at similar Plith–T conditions (650–700°C, 5–6 kbar) in the presence of carbonic fluids internally buffered by reaction with graphite and opaque mineral phases (XCO2= 0.7–0.6; XH2O= 0.2–0.3; XN2= 0.1; log fO2= -17.5). Mineralogical zonation indicates that charnockitization of the leptynitic gneiss involved first the breakdown of biotite and oxidation of graphite in narrow, outward-migrating transition zones adjacent to the gneiss, followed by the breakdown of garnet and the neoblastesis of hypersthene in the central charnockite zone. Compared to the host gneiss, the charnockite shows higher concentrations of K, Na, Sr, Ba and Zn and lower concentrations of Mg, Fe, Ti, V, Y, Zr and the HREE, with a complementary pattern in the narrow transition zones of biotite breakdown. The Plith–T–XH2O data and chemical zonation patterns indicate charnockitization through subsolidus-dehydration reaction in an open system. Subsequent residence of the carbonic fluids in the charnockite resulted in low-grade alteration causing modification of the syn-charnockitic elemental distribution patterns and the properties of entrapped fluids. We favour an internally controlled process of arrested charnockitization in which, during near-isothermal uplift, the release of carbonic fluids from decrepitating inclusions in the host gneiss into simultaneously developing fracture zones led to a change in the fluid regime from ‘fluid-absent’in the gneiss to ‘fluid-present’in the fracture zones and to the development of an initial fluid-pressure gradient, triggering the dehydration reaction.  相似文献   

3.
Analyses of 80 biotite, alkali feldspar, oligoclase, hornblende, Fe-Ti oxide separates from the coarse-grained granites of a late-hercynian epizonal diapir, the Ploumanac'h complex, Brittany, show that these minerals display a regular concentric cryptic layering related to fractional crystallization. The Ca, Mg, Ba, Sr, Cr, V content of minerals decreases as the Na, Fe, and Rb content increases. Biotites become more dioctahedral towards the outer residual syenogranite, with a correlative K deficiency. Trioctahedral biotites from the inner accumulative monzogranite are secondarily oxidized with a gain of Fe3+ and a loss of OH. This alteration id due to the percolation of exsolved fluids rich in H2O and containing a small amount of CO2, F, S, Cl. During this autometamorphic stage, trace elements like Rb, Sr are completely redistributed on the scale of hand specimens, with a restricted range of partition coefficients between biotite, perthite and oligoclase. This equilibration occurred at a temperature about 550 ° C and a fluid pressure about 1,000 bars, with f H2O probably less than 500 bars. A later stage of fluid circulation along fractures brings up a slight Li metasomatism. Biotites are a sensitive marker of both magmatic and postmagmatic stages of subsolvus or ‘wet’ plutonites.  相似文献   

4.
Multiphase solid inclusions in minerals formed at ultra-high-pressure (UHP) provide evidence for the presence of fluids during deep subduction. This study focuses on barian mica, which is a common phase in multiphase solid inclusions enclosed in garnet from mantle-derived UHP garnet peridotites in the Saxothuringian basement of the northern Bohemian Massif. The documented compositional variability and substitution trends provide constraints on crystallization medium of the barian mica and allow making inferences on its source. Barian mica in the multiphase solid inclusions belongs to trioctahedral micas and represents a solid solution of phlogopite KMg3(Si3Al)O10(OH)2, kinoshitalite BaMg3(Al2Si2)O10(OH)2 and ferrokinoshitalite BaFe3(Al2Si2)O10(OH)2. In addition to Ba (0.24–0.67 apfu), mica is significantly enriched in Mg (XMg ~ 0.85 to 0.95), Cr (0.03–0.43 apfu) and Cl (0.04–0.34 apfu). The substitution vector involving Ba in the I-site which describes the observed chemical variability can be expressed as BaFeIVAlClK?1Mg?1Si?1(OH)?1. A minor amount of Cr and VIAl enters octahedral sites following a substitution vector VI(Cr,Al)2□VI(Mg,Fe)?3 towards chromphyllite and muscovite. As demonstrated by variable Ba and Cl contents positively correlating with Fe, barian mica composition is partly controlled by its crystal structure. Textural evidence shows that barian mica, together with other minerals in multiphase solid inclusions, crystallized from fluids trapped during garnet growth. The unusual chemical composition of mica reflects the mixing of two distinct sources: (1) an internal source, i.e. the host peridotite and its garnet, providing Mg, Fe, Al, Cr, and (2) an external source, represented by crustal-derived subduction-zone fluids supplying Ba, K and Cl. At UHP–UHT conditions recorded by the associated diamond-bearing metasediments (c. 1100 °C and 4.5 GPa) located above the second critical point in the pelitic system, the produced subduction-zone fluids transporting the elements into the overlying mantle wedge had a solute-rich composition with properties of a hydrous melt. The occurrence of barian mica with a specific chemistry in barium-poor mantle rocks demonstrates the importance of its thorough chemical characterization.  相似文献   

5.
The Early Cretaceous Duolong gold‐rich porphyry copper deposit is a newly discovered deposit with proven 5.38 Mt Cu resources of 0.72% Cu and 41 t gold of 0.23 g t?1 in northern Tibet. Granodiorite porphyry and quartz diorite porphyrite are the main ore‐bearing porphyries. A wide range of hydrothermal alteration associated with these porphyries is divided into potassic, argillic and propylitic zones from the ore‐bearing porphyry center outward and upward. In the hydrothermal alteration zones, secondary albite (91.5–99.7% Ab) occurs along the rim of plagioclase phenocryst and fissures. Secondary K‐feldspar (75.1–96.9% Or) replaces plagioclase phenocryst and matrix or occurs in veinlets. Biotite occurs mainly as matrix and veinlet in addition to phenocryst in the potassic zone. The biotite are Mg‐rich and formed under a highly oxidized condition at temperatures ranging from 400°C to 430°C. All the biotites are absent in F, and have high Cl content (0.19–0.26%), with log (XCl/XOH) values of ?2.74 to ?2.88 and IV (Cl) values of ?3.48 to ?3.35, suggesting a significant role of chloride complexes (CuCl2‐ and AuCl2‐) in transporting and precipitating copper and gold. Chlorites are present in all alteration zones and correspond mainly to pycnochlorite. They have similar Fe/(Fe+Mg), Mn/(Mn+Mg) ratios, and a formation temperature range of 280–360°C. However, the formation temperature of chlorite in the quartz‐gypsum‐carbonate‐chlorite vein is between 190°C and 220°C, indicating that it may have resulted from a later stage of hydrothermal activity. Fe3+/Fe2+ ratios of chlorites have negative correlation with AlIV, suggesting oxygen fugacity of fluids increases with decreasing temperature. Apatite mineral inclusions in the biotite phenocrysts show high SO3 content (0.44–0.82%) and high Cl content (1–1.37%), indicating the host magma had a high oxidation state and was enriched in S and Cl. The highest Cl content of apatite in the propylitic zone may have resulted from pressure decrease, and the lowest Cl content of apatite in the argillic zone may have been caused by a low Cl content in the fluids. The low concentration of SO3 content in the hydrothermal apatite compared to the magmatic one may have resulted from the decrease of oxygen fugacity and S content in the hydrothermal fluid, which are caused by the abundant precipitation of magnetite.  相似文献   

6.
The hydroxyl (O(4)) site composition of biotite can in principle be used to retrieve information about fluid composition during fluid–rock interaction; however, due to low F and Cl content, as well as difficulties involved with analyzing the H2O content using in situ techniques, measuring these species in biotite has remained an elusive goal. Here we present high-precision secondary ion mass spectrometry (SIMS) OH–F–Cl measurements from biotite within metapelites from the Western Adamello Tonalite (WAT) contact aureole, Northern Italy. Fluorine, chlorine and hydrogen are analyzed on the SIMS sequentially by peak-hopping at the same biotite spot; H2O, F and Cl content were measured with a precision (1σ) οφ 0.06 ωτ%, 50 ανδ 5 ππµ, ρεσπεχτι?ελψ. The compositions of isolated biotite crystals in andalusite are compared with that of biotite in the matrix, documenting that halogens and H2O behave refractory in biotite during the time scale of contact metamorphism. The H2O and halogen contents of biotite are mostly locked in during the prograde to peak formation of biotite, and are not reset during further heating or cooling, unless significant biotite recrystallization occurs. It also appears that both Ti content and XMg of the biotite from the Western Adamello contact aureole were not significantly reset during cooling. The concentration of F and Cl does not vary systematically with metamorphic grade, which indicates that these species reflect initial compositions. No significant Rayleigh fractionation behavior was observed for these elements. H2O variations in the biotite from samples throughout the Western Adamello contact aureole suggest that Al-oxy substitution partially controls the variations in OH content through charge balance of the type R2+,VI + OH? = Al3+,VI + O2? + H2, while the Ti-oxy substitution does not seem to influence the O(4) site occupation. The main titanium substitution appears to be the Ti-vacancy (\({\text{2}}{{\text{R}}^{{\text{2}}+}}~=~{\text{T}}{{\text{i}}^{{\text{4}}+}}~+\,{\square ^{{\text{VI}}}}\)) exchange. Variations in H2O and halogen concentrations in biotite define sub mm-scale areas of localized equilibration, even for biotite recrystallized during dehydration reactions that produced large amounts of fluid (chlorite or muscovite breakdown). Similar systematics were observed for Ti4+ and Al3+. These findings further support the increasing number of observations that kinetics control much of the mineralogical reactions occurring in contact aureoles, and hence care is advised in using equilibrium thermodynamics in this environment.  相似文献   

7.
A Permo-Triassic pelite-carbonate rock series (with interacalated metabasitic rocks) in the Cordilleras Béticas, Spain, was metamorphosed during the Alpine metamorphism at high pressures (P min near 18 kbar). The rocks show well preserved sedimentary features of evaporites such as pseudomorphs of talc, of kyanite-phengitetalc-biotite, and of quartz after sulfate minerals, and relicts of baryte, anhydrite, NaCl, and KCl, indicating a salt-clay mixture of illite, chlorite, talc, and halite as the original rock. The evaporitic metapelites have a whole rock composition characterized by high Mg/(Mg+Ca) ratios>0.7, variable alkaline and Sr, Ba, contents, but are mostly K2O rich (<8.8 wt%). The F (<2600 ppm), Cl (<3600 ppm), and P2O5 (<0.24 wt%) contents are also high. The pelitic member of this series is a fine grained biotite rock. Kyanite-phengite-talc-biotite aggregates in pseudomorphs developed in the high pressure stage. Albite-rich plagioclase was formed when the rocks crossed the albite stability curve in the early stages of the uplift. Scapolite, rich in NaCl (Ca/(Ca+Na) mol% 24–40) and poor in SO4, with Cl/(Cl+CO3) ratios between 0.6 and 0.8, formed as porphyroblasts, sometimes replacing up to 60% of the rock in a late stage of metamorphism (between 10 and 5 kbar, near 600°C). No reaction with albite is observed, and the scapolite formed from biotite by: $$\begin{gathered} Al - biotite + CaCO_3 + NaCl + SiO_2 \hfill \\ = Al - poor biotite + scapolite + MgCO_3 + KCl \hfill \\ + MgCl_2 + H_2 O \hfill \\ \end{gathered}$$ Calculated fluid composition in equilibrium with scapolite indicates varying salt concentrations in the fluid. Distribution of Cl and F in biotite and apatite also indicates varying fluid compositions.  相似文献   

8.
The Fe-Mg-Ca-distribution was investigated in synthesis experiments and with the mineral assemblage orthopyroxene+clinopyroxene+quartz. The phase compositions were identified by X-ray diffraction and, where possible, by electron microprobe. The attainment of equilibrium in the run products was signalled by the compositions from control runs (different solutions) becoming closely similar, by recycling runs, by the attainment of equilibrium from different directions (depending on the composition of starting phases), and by special kinetic experiments.The study produced the following results: (1) the Ca content of the clinopyroxenes decreases with increasing Fe (mol%) from 48.4 at X Cpx Fe =5 to 39.8 at X Cpx Fe =45 (800° C); from 47.6 at X Cpx Fe = 10 to 41.7 at X Cpx Fe =45 (750° C); increasing temperature expands the stability field of the less calcic clinopyroxenes. (2) The Ca content of orthopyroxenes increases slightly with Fe content from 1.8 at X Opx Fe =20.5 to 3.2 at X Opx Fe =75; the temperature effect on the Ca content under the T, P conditions of the experiment was not large. (3) Fe and Mg distribution between the coexisting ortho-and clinopyroxenes is largely temperature-dependent, particularly in the compositional range X Opx Fe =15–75 mol%; as T increases, Fe redistributes from the rhombic to monoclinic mineral.Preliminary estimates of rock formation temperatures using the obtained data show that most of the known two-pyroxene geothermometers overstate the actual values by 50–150° C.  相似文献   

9.
Baotite occurs as a late phase in the Kval?ya lamproite dyke and in the fenitized granite adjacent to the dyke, suggesting that baotite formed during reactions between rock and fluids derived from a volatile-rich lamproitic magma. Most of the analyzed grains of baotite from the Kval?ya lamproite show compositions close to the ideal Nb-free end-member Ba4Ti8Si4O28Cl. Compilation of all published baotite analyses suggests that the major compositional variations of baotite occur between the Nb-free end member Ba4Ti8Si4O28Cl, and a Nb-rich end member Ba4Ti2Fe2+ 2Nb4Si4O28Cl. However, a Pb-bearing baotite, showing significant concentrations of Ca, Sr, Pb and K, and approximately 3 Ba p.f.u., was also identified from the Kval?ya lamproite. Euhedral fluorapatite formed as an early phase during crystallization of the lamproite magma, while anhedral REE-rich fluorapatite overgrowths on the euhedral grains formed during reactions with the late magmatic fluid. Fluorapatite contains up to 1.2?F p.f.u., but only traces of Cl. Other F-rich, but Cl-poor minerals of the lamproite include fluoro-potassic-magnesio-arfvedsonite, fluoro-phlogopite, and yangzhumingite. The presence of baotite together with a range of high-F, but low-Cl mineral phases suggests that the minerals formed in equilibrium with a high-F, Cl-bearing hydrous fluid. The high Cl-content of baotite demonstrates that Cl is strongly partitioned into this mineral in the presence of a Cl-bearing F-rich hydrous fluid. We suggest that a combination of high aSi, aTi, aBa, and fO2, but low aCa of the fluid enabled baotite formation.  相似文献   

10.
The chemical compositions of rock-forming minerals have been determined for both altered and least-altered igneous rocks spatially associated with numerous mineralized zones (Nucleus Au–Bi–Cu–As deposit, Revenue Au ± Cu and Stoddart Cu–Mo ± W mineral occurrences, and Laforma Au–Ag deposit) across the Freegold Mountain area, Yukon, Canada. Within the study area, K-feldspar has a narrow compositional range (89.4–91% Or), whereas plagioclase spans a wide range (4.4–70.07% An). In all of the investigated samples, T Ab = T An = T Or, suggesting that magmatic equilibrium between the coexisting plagioclase and K-feldspar was maintained. Igneous amphibole phenocrysts from hypabyssal dikes are typically calcic, whereas the Stoddart Cu–Mo ± W, Laforma Au–Ag, and Goldy Au mineralization are associated with Mg-enriched primary amphibole of edenite composition, and Au–Bi–Cu–As mineralization from Nucleus is related to Al-enriched primary amphibole of ferropargasite composition. Primary biotite phenocrysts across the Freegold Mountain area re-equilibrated with oxidized magma (f(O2) values between 10–13 and 10–11.5 bars, lying between the Ni/NiO and the magnetite/haematite buffers). However, biotite and amphibole phenocrysts from Stoddart, Goldy, Laforma, and the Highway zones crystallized from a more oxidized magma, as indicated by their elevated X Mg up to 0.65, relative to biotite and hornblende from Nucleus and Revenue characterized by a lower X Mg (typically < 0.50). This suggests that various sources and (or) rapid emplacement were involved in magma genesis, as further supported by the considerable variation of pressure (1.8–7.3 kb) of amphibole crystallization and of the total Al content in least-altered biotite (2.6–2.9 afu) within the Freegold Mountain area. Biotite and apatite equilibrated within the T range of 520–780°C, consistent with temperatures of equilibration between ilmenite and magnetite, and their compositions indicate that they formed from an oxidized I-type magma. Magma differentiated by fractional crystallization (indicated by the presence of normally zoned plagioclase with Ca-rich cores and Na-enriched outer rims) and multiple magma mixing (supported by the presence of reversed zoned plagioclase and coexistence of normally and reversely zoned plagioclase). Lower X Mg biotite associated with the mineralized (Cu–Mo ± W) potassic alteration incorporated more F and Cl relative to least-altered biotite with higher X Mg. In both Nucleus and Revenue Au–Cu mineralizations, secondary biotite composition varies with respect to the associated alteration mineral assemblages. Although secondary biotite in the skarn re-equilibrated with F-poor fluids, secondary biotite from the pervasive biotitization is related to F- and Cl-enriched fluids, and secondary biotite from the phyllitic zone is related to F-, Cl-, and Mg-depleted fluids, thus consistent with a change in mineralizing fluid composition during mineralization.  相似文献   

11.
Spectacular reaction textures in poikiloblastic scapolitite boudins, within marbles in the continental crust exposed in the Lützow–Holm Complex, East Antarctica, provide insights into the changing fluid composition and movement of fluid along grain boundaries and fractures. Petrographic and geochemical features indicate scapolite formation under contrasting fluid compositions. Core composition of scapolite poikiloblasts (ScpI) are marialitic (Cl = 0.7 apfu) whereas rims in contact with biotite or clinopyroxene are meionite rich. Fine‐grained recrystallized equigranular scapolite (ScpII) shows prominent chemical zoning, with a marialitic core and a meionitic rim (Cl = 0.36 apfu). Scapolite poikiloblasts are traversed by ScpIII reaction zones along fractures with compositional gradients. Pure CO2 fluid inclusions are observed in healed fractures in scapolite poikiloblasts. These negative crystal‐shaped fluid inclusions are moderately dense, and are believed to be coeval with ScpIII formation at temperatures >600 °C and a minimum pressure of c. 3.8 kbar. Grain‐scale LA‐ICPMS studies on trace and rare earth elements on different textural types of scaplolites and a traverse through scapolite reaction zone with compositional gradient suggest a multistage fluid evolution history. ScpI developed in the presence of an internally buffered, brine‐rich fluid derived probably from an evaporite source during prograde to peak metamorphism. Recrystallization and grain size reduction occurred in the presence of an externally sourced carbonate (CaCO3)‐bearing fluid, resulting in the leaching of Cl, K, Rb and Ba from ScpI along fractures and grain boundaries. Movement of fluids was enhanced by micro‐fracturing during the transformation of ScpI to ScpIII. Fractures in fluorapatite are altered to chlorapatite proving evidence for the pathways of escaping Cl‐bearing fluids released from ScpI. The present study thus provides evidence for the usefulness of scapolite in fingerprinting changing volatile composition and trace element contents of fluids that percolate within the continental crust.  相似文献   

12.
Garnet-biotite gneisses, some of which contain sillimanite or hornblende, are widespread within the Otter Lake terrain, a portion of the Grenville Province of the Canadian Shield. The metamorphic grade is upper amphibolite to, locally, lower granulite facies. The atomic ratio Fe2+/(Fe2++ Fe3+) in biotite ranges from 0.79 to 0.89 (ferrous iron determinations in 10 highly pure separates), with a mean of 0.86. Mg and Fe2+ atoms occupy 67–78% of the octahedral sites, the remainder are occupied by Fe3+, Ti, and Al, and some are vacant. Mg/(Mg + Fe2+), denoted X, in the analysed samples ranges from 0.32 to 0.65. Garnet contains 1–24% grossular, 1–12% spessartine and X ranges from 0.07 to 0.34. Compositional variation in biotite and garnet is examined in relation to three mineral equilibria: (I) biotite + sillimanite + quartz = garnet + K-feldspar + H2O; (II) pyrope + annite = almandine + phlogopite; (III) anorthite = grossular + sillimanite + quartz. Measurements of X (biotite) and X (garnet) are used to construct an illustrative model for equilibrium (I) which relates the observed variation in X to a temperature range of 70°C or a range in H2O activity of 0.6; the latter interpretation is preferred. In sillimanite-free gneisses, the distribution of Mg and Fe2+ between garnet (low in Ca and Mn) and biotite is adequately described by a distribution coefficient (KD) of 4.1 (equilibrium II). The observed increase in the distribution coefficient with increasing Ca in garnet is ln KD= 1.3 + 2.5 × 10?2 [Ca] where [Ca] = 100 Ca/(Mg + Fe2++ Mn + Ca). The distribution coefficient is apparently unaffected by the presence of up to 12% spessartine in garnet. In several specimens of garnet-sillimanite-plagioclase gneiss, the Ca contents of garnet and of plagioclase increase in unison, as required by equilibrium (III). The mean pressure calculated from these data (n= 17) is 5.9 kbar, and the 95% confidence limits are ±0.5 kbar.  相似文献   

13.
Garnet–biotite–(sillimanite) gneiss (～700 °C, 7 kbar) of the Otter Lake area in the Western Grenville Province (Canadian Shield) occurs as granitic gneiss (group 4) that forms a large part of the Otter Complex, and as widely distributed, more heterogenous metasedimentary gneiss (group 2). In one sample of group 4 gneiss (Qtz25 Pl34 Kfs28 Bt10 Grt2.5 Sil1) the true diameter (determined by serial grinding) of subhedral garnet crystals ranges from 0.2 to 3.0 mm, with a mode at 1.0 mm. Nearest‐neighbour measurements in this sample, and in surfaces of nine additional samples (all <5% garnet) confirm that garnet crystals are distributed mainly at random; slight clustering was detected in two samples. In one sample of group 4 gneiss, microprobe analyses on sections through crystal centres (obtained by serial slicing), reveal that small crystals and margins to large crystals contain more Fe and Mn and less Mg than the broad central regions of large crystals. Based on these and previous results, together with theoretical considerations, a crystallization model is proposed, in which, (i) garnet was produced by the continuous reaction, Ms + Bt + Qtz → Grt + Kfs + H2O, (ii) nucleation occurred by the random selection of randomly distributed Ms–Bt–Qtz triple junctions, (iii) the rate of linear growth remained constant, and (iv) as temperature increased, the rate of nucleation first increased slowly, then remained nearly constant, and finally declined. Within‐population compositional homogenization was followed, on cooling, by local Fe–Mg–Mn exchange with biotite.  相似文献   

14.
The zonal structure of prograde garnet in pelitic schists from the medium-grade garnet zone and the higher-grade albite-biotite zone was examined to investigate the evolution of prograde P–T paths of the Sanbagawa metamorphism. The garnet studied shows a bell-shaped chemical zoning of the spessartine component, which decreases in abundance from the core towards the rim. Almandine and pyrope contents and XMg [=Mg/(Mg+Fe2+)] increase monotonously outwards. The general scheme of the zonal structure for grossular content [XGrs=Ca/(Fe2++Mn+Mg+Ca)] can be summarized as: (1) XGrs increases outwards (inner segment) and reaches a maximum at an intermediate position between the crystal core and the rim, then decreases towards the outermost rim (outer segment) (2) the inner segment of garnet in the garnet zone samples tends to have a higher XGrs/XSps values for a given XSps than those in the albite–biotite zone samples (3) average XSps at the maximum XGrs position in the albite–biotite zone samples ranges from 0.02 to 0.12 and is lower than that in the garnet zone samples (0.13–0.32) (4) the maximum XGrs in the albite–biotite zone samples (0.34–0.39 on average) tends to be higher than that in the garnet zone samples (0.26–0.36), and (5) differences of XGrs between the maximum and rim in the albite–biotite zone samples are between 0.10 and 0.14 and higher than those in the garnet zone samples (< 0.11). These facts imply that albite–biotite zone materials (a) were recrystallized under lower dP/dT conditions at an early stage of the prograde metamorphism (b) began their exhumation under higher P–T conditions and (c) have been continuously heated during exhumation for a longer duration than the garnet zone materials. The systematic changes of prograde P–T paths can be interpreted as documenting the evolution of the Sanbagawa subduction zone.  相似文献   

15.
阳储岭斑岩型W-Mo矿床位于江南造山带中部,是华南地区最早发现的斑岩型钨钼矿床。已探明WO3资源储量6.13万吨(平均品位0.2%),Mo资源储量1.69万吨(平均品位0.03%～0.06%),其成矿作用与中生代花岗质岩浆活动密切相关。区内发育早期花岗闪长岩和晚期二长花岗斑岩,钨矿体以细脉状和浸染状产于二长花岗斑岩体内,而花岗闪长岩内未见矿化。两期岩浆活动与钨成矿的关系尚不明确,制约其含矿差异性的因素尚不清楚。本文以花岗闪长岩和二长花岗斑岩中的黑云母为研究对象,对比研究两类岩浆结晶分异程度、氧逸度、岩浆流体卤素浓度,探讨其对钨成矿的制约。黑云母主量元素分析结果显示,阳储岭两类岩浆岩均为壳源,但显著不同于S型花岗岩的Mg/(Fe+Mg)和AlVI值,指示其具有I型花岗岩的特征。黑云母的微量元素信息显示,相对于花岗闪长岩中的黑云母(类型一),二长花岗斑岩中的黑云母(类型二)显示低的K/Rb、Nb/Ta比值,高的Rb、Cs、Nb和Ta含量,表明其分异程度较花岗闪长岩更高,更有利于钨的富集。两类黑云母所指示的岩浆氧逸度均在NNO缓冲线附近,表明其母岩...  相似文献   

16.
Minerals of the triphylite-lithiophilite, Li(Fe, Mn)PO4, and the triplite-zwieselite-magniotriplite series, (Mn, Fe, Mg)2PO4F, occur in the late stage period of pegmatite evolution. Unfortunately, neither are the genetic relationships between these phosphates fully understood nor are thermodynamic data known. Consequently, phosphate associations and assemblages from 8 granitic pegmatites — Clementine II, Rubicon II and III, and Tsaobismund (Namibia); Hagendorf-Süd and Rabenstein (Germany); Valmy (France); Viitaniemi (Finland) — have been tested for compositional zoning and intercrystalline partitioning of main elements by electron microprobe techniques. Although the selected pegmatites display varying degrees of fractionation, and the intergrowth textures indicate different genetic relationships between the phosphates, the plots of mole fractions X Fe=Fe/(Fe+Mn+Mg+Ca), X Mn=Mn/(Fe+Mn+Mg+Ca), and X Mg=Mg/(Fe+Mn+Mg+Ca) can be fitted relatively well with smooth curves in Roozeboom diagrams. Their deviations from symmetrical distribution curves are mainly dependent upon X Mg or X Ca, and upon non-ideal solutions. Surprisingly small differences between the partition coefficients were detected for intergrowths of different origin. However, the partitioning of shared components among coexisting phases is clearly dependent upon the conditions of formation. Compositional zoning is observed only when both Fe–Mn phosphates are intergrown mutually or with other Fe–Mn–Mg mineral solid-solutios. Thus, the zoning does not seem to be due to continuous crystallization, but to later diffusion processes. The triplite structure has preference for Mn, Mg, and Ca, while Fe prefers minerals of the triphylite series. A quantification of main element fractionation between minerals of the triphylite and the triplite series is possible in the cases where diffusion can be excluded. For the Fe/(Fe+Mn) ratios of core compositions an equation with a high correlation coefficient (R=0.988) was determined: Fe/(Fe+Mn)Tr=[Fe/(Fe+Mn)Li]/{2.737-(1.737)[Fe/(Fe+Mn)Li]} (Tr=triplite series, Li=triphylite series). Consequently, the Fe/(Fe+Mn) ratio of the triplite series can now also be used in the interpretation of pegmatite evolution, just like that of the triphylite series which has been successfully applied in the past.  相似文献   

17.
Pumpellyite of the general formula W8X4Y8-Z12O56-n(OH)n contains Fe, Al and Mg in two crystallographically different octahedral sites. Three different pumpellyite samples covering the known compositional field from Al- to Fe-rich have been studied to determine the valence state and intracrystalline partitioning of the Fe cations between the two independent octahedral sites. Fe+2 and Fe+3 cation partitioning is interpreted on the basis of results obtained by 57Fe Mössbauer spectroscopy at 293 and 77 K and from Rietveld structure analysis performed on powder X-ray diffraction data. Pumpellyite from low-grade metamorphic rocks typically contains a majority of iron in the Fe+3 oxidation state, which is found in the smaller and less symmetrical octahedral Y-site. Fe+2 was also present in all pumpellyite samples studied and it is located in the larger and more symmetrical octahedral X-site.  相似文献   

18.
Published experimental data including garnet and clinopyroxene as run products were used to develop a new formulation of the garnet–clinopyroxene geothermometer based on 333 garnet–clinopyroxene pairs. Only experiments with graphite capsules were selected because of difficulty in estimating the Fe3+ content of clinopyroxene. For the calibration, a published subregular‐solution model was adopted to express the non‐ideality of garnet. The magnitude of the Fe–Mg excess interaction parameter for clinopyroxene (WFeMgCpx), and differences in enthalpy and entropy of the Fe–Mg exchange reaction were regressed from the accumulated experimental data set. As a result, a markedly negative value was obtained for the Fe–Mg excess interaction parameter of clinopyroxene (WFeMgCpx = ? 3843 J mol?1). The pressure correction is simply treated as linear, and the difference in volume of the Fe–Mg exchange reaction was calculated from a published thermodynamic data set and fixed to be ?120.72 (J kbar?1 mol?1). The regressed and obtained thermometer formulation is as follows: where T = temperature, P = pressure (kbar), A = 0.5 Xgrs (Xprp ? Xalm ? Xsps), B = 0.5 Xgrs (Xprp ? Xalm + Xsps), C = 0.5 (Xgrs + Xsps) (Xprp ? Xalm), Xprp = Mg/(Fe2+ + Mn + Mg + Ca)Grt, Xalm = Fe/(Fe2+ + Mn + Mg + Ca)Grt, Xsps = Mn/(Fe2+ + Mn + Mg + Ca)Grt, Xgrs = Ca/(Fe2+ + Mn + Mg + Ca)Grt, XMgCpx = Mg/(Al + Fetotal + Mg)Cpx, XFeCpx = Fe2+/(Al + Fetotal + Mg)Cpx, KD = (Fe2+/Mg)Grt/(Fe2+/Mg)Cpx, Grt = garnet, Cpx = clinopyroxene. A test of this new formulation to the accumulated data gave results that are concordant with the experimental temperatures over the whole range of the experimental temperatures (800–1820 °C), with a standard deviation (1 sigma) of 74 °C. Previous formulations of the thermometer are inconsistent with the accumulated data set; they underestimate temperatures by about 100 °C at >1300 °C and overestimate by 100–200 °C at <1300 °C. In addition, they tend to overestimate temperatures for high‐Ca garnet (Xgrs ≈ 0.30–0.50). This new formulation has been tested against previous formulations of the thermometer by application to natural eclogites. This gave temperatures some 20–100 °C lower than previous formulations.  相似文献   

19.
The cation exchange reaction Fe3Al2Si3O12 +KMg3AlSi3O10(OH)2 = Mg3Al2Si3O12+KFe3-AlSi3 O10(OH)2 has been investigated by determining the partitioning of Fe and Mg between synthetic garnet, (Fe, Mg)3Al2Si3O12, and synthetic biotite, K(Fe, Mg)3AlSi3O10(OH)2. Experimental results at 2.07 kbar and 550 °–800 ° C are consistent with In [(Mg/Fe) garnet/(Mg/Fe) biotite] = -2109/T(°K) +0.782. The preferred estimates for ¯H and ¯S of the exchange reaction are 12,454 cal and 4.662 e.u., respectively. Mixtures of garnet and biotite in which the ratio garnet/biotite=49/1 were used in the cation exchange experiments. Consequently the composition of garnet-biotite pairs could approach equilibrium values in the experiments with minimal change in garnet composition (few tenths of a mole percent). Equilibrium was demonstrated at each temperature by reversal of the exchange reaction. Numerical analysis of the experimental data yields a geothermometer for rocks containing biotite and garnet that are close to binary Fe-Mg compounds.  相似文献   

20.
黑云母是花岗质岩石中常见的造岩矿物,其成分可以有效指示花岗岩形成的物理化学条件和岩石成因。巴斯铁列克矿床是近年来在新疆阿尔泰造山带南缘发现的首例二叠纪矽卡岩型钨多金属矿床。矿区出露多种类型二叠纪含钨花岗岩。为理清花岗质岩体之间、岩体与钨多金属矿化之间的关系,文章采用电子探针测定了黑云母花岗岩、二长花岗岩、二云母花岗岩和钾长花岗岩中的黑云母成分。结果表明,所有黑云母具有富铁、高铝、贫镁特征,含铁指数(Fe2+/(Mg+Fe2+))为0.66~0.80,二云母花岗岩属铁质黑云母而黑云母花岗岩、二长花岗岩和钾长花岗岩属铁叶黑云母。所有岩石是具有A型特征的I型花岗岩。不同类型岩石中黑云母的成分差异与岩浆来源、分异演化程度有关。二云母花岗岩中黑云母的w(MgO)与结晶温度最高,与黑云母平衡流体的log(fHF/fHCl)值（-1.13~-1.25）最低,log(fH2O/fHF)值（4.64~4.96）最高,母岩浆相对富Cl;黑云母花岗岩中log(fHF/fHCl)值最高,log(fH2O/fHF)最低,与二长花岗岩是同一岩浆房不同演化阶段的产物,与二云母花岗岩和钾长花岗岩属不同的岩浆体系,母岩浆相对富F元素。黑云母花岗岩与W矿化关系更密切。  相似文献   

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