共查询到20条相似文献，搜索用时 565 毫秒
1.
Sudoite, with almost ideal composition of Mg2Al4Si3O10(OH)8, has been found in the Khaki shale of the Witwatersrand Basin, South Africa. The sudoite occurs in aggregates of elongate bundles alternating with muscovite and rarely pyrophyllite, in an assemblage of sudoite-pyrophyllite-muscovite-quartz-rutile-pyrite. The stability of sudoite is attributed to a particularly Mg rich bulk rock composition, elevated sulphur activity, and metamorphic conditions just above the kaolinite to pyrophyllite transition. Nearby low variance chlorite, chloritoid-and pyrophyllite-bearing assemblages represent differing bulk rock compositions at potentially very similar metamorphic conditions. As the first find of sudoite in the Archaean, this occurrence in the Witwatersrand Basin extends the metamorphic setting and age in which sudoite is found to well beyond Phanerozoic belts of crustal thickening. 相似文献
2.
Sudoite, ideally (Mg2Al3)[AlSi3O10](OH)8, was synthesized in small quantities from a number of starting materials using seeds of the natural mineral. Because its powder X-ray diffraction pattern is very similar to that of normal, trioctahedral chlorite, a technique based on relative intensities of 001-peaks of the chlorite-type phases was used, in addition to the standard X-ray method, to determine growth or breakdown of sudoite. Seeded runs indicate that sudoite is more stable than at least five alternative mineral assemblages in the system MgO-Al2O3-SiO-H2O below about 370°–390° C at water pressures up to at least 7 kbar. At higher temperatures sudoite decomposes into assemblages of normal chlorite with an Al2SiO5-phase and either quartz or pyrophyllite. However, the exact locations of the univariant breakdown curves could not be determined due to very low reaction rates. Schreinemakers analyses indicate that the assemblage sudoite+quartz represents the low-temperature equivalent of the common pair chlorite+pyrophyllite, and that sudoite+quartz is limited to water pressures below about 7 kbar because of its reaction to form the high-pressure phase Mg-carpholite; however, in the absence of quartz, the stability fields of sudoite and of Mg-carpholite overlap at pressures above 7 kbar.These stability data are in general agreement with two well-documented sudoite occurrences in quartz veins cutting highly oxidized, low-pressure manganiferous metapelites, and with one occurrence in a silica-deficient high-pressure metamorphic metabauxite. Sudoites may be more common in low-grade metamorphic rocks than known thus far, but they may not be stable under surface conditions. 相似文献
3.
H. J. Tobschall 《Contributions to Mineralogy and Petrology》1969,24(1):76-91
In the middle part of the Cévennes, situated at the south-eastern border of the Massif Central, there are outcrops of micaschists, gneisses and granites in which the increase of metamorphic grade was investigated along the river Beaume. This paper presents the results of the petrographic-geochemical analysis of the micaschists of the greenschist facies.Chemical analyses of the micaschist-samples examined petrographically show their nearly constant composition, a fact which e.g., is expressed by similar CaO/Na2O- and MgO/FeO-proportions. As the average values of the determined oxides approach the respective average values of analyses of graywackes recorded by Pettijohn (1957) the original sediment is likely to have been an argillaceous graywacke deficient in calcite.In enrichments of the phyllosilicates pyrophyllite was detected by X-ray diffraction; its amount is about 2 to 5 weight percent of the rocks.With increasing metamorphic grade the following parageneses were found in the metamorphic zones of the greenschist facies:
Zone Ia: Quartz+chlorite+pyrophyllite+muscovite+clinozoisite.
Zone Ib: Quartz+chlorite+pyrophyllite+muscovite+biotite+clinozoisite.The absence of biotite in Zone Ia, though the chemism of the rocks is practically the same, is obviously due to the different Al2O3-content of the chlorites of Zones Ia and Ib. The chlorite of Zone Ia is more deficient in Al2O3 than the one of Zone Ib. With passage from Zone Ia to Zone Ib the position of the tie line between chlorite and muscovite in the ACF-A'FK-diagram changes in such a way that in Zone Ia, because of purely chemical reasons, biotite cannot occur as coexisting mineral.The beginning of Zone II is characterized by the occurence of almandine, rich in spessartine. The following paragenesis is typical of this zone: Quartz+chlorite+pyrophyllite +muscovite+biotite+almandine+clinozoisite.Additionally the micaschists of these three zones display albite, the greater part of which is concentrated in mm-thin layers with associated minor amounts of quartz and micas. Paragonite whose formation by reaction between albite and pyrophyllite is to be expected based on experimental results (Winkler, 1967, p. 95) could not be proved by X-ray diffraction.In Zone III andalusite occurs instead of pyrophyllite. Furthermore, as chlorite and clinozoisite are absent and oligoclase occurs for the first time this zone is regarded as the first subfacies of the almandine-amphibolite-facies. The chemism and the observed mineral parageneses of the subfacies of the almandine-amphibolite-facies will be treated in a separate publication. 相似文献
4.
《Geochimica et cosmochimica acta》1999,63(19-20):3193-3203
Formation of secondary Ni precipitates is an important mechanism of Ni retention in neutral and alkaline clay/water systems. However, the structure and composition of these secondary phases, and their stability is still disputable. Using existing structure refinement data and new ab-initio FEFF 7 calculations we show that Ni-edge X-ray absorption fine structure spectroscopy alone may not be able to unequivocally discriminate four possible candidate compounds: α-Ni(OH)2, the isostructural but Al-substituted layered double hydroxide (Ni-Al LDH), and 1:1 and 2:1 Ni-containing phyllosilicates. Hence, we investigated the potential of diffuse reflectance spectroscopy (DRS) in determining in situ the Ni phase forming in the presence of four sorbents, pyrophyllite, talc, gibbsite, and amorphous silica. The 3A2g → 3T1g(F) band (ν2) of octahedrally coordinated Ni2+ could be reliably extracted from the reflectance spectra of wet pastes. In the presence of the Al-free talc and amorphous silica, the ν2 band was at ≈14,900 cm−1, but shifted to 15,300 cm−1 in the presence of Al-containing pyrophyllite and gibbsite. This shift suggests that Al is dissolved from the sorbent and substitutes for Ni in brucite-like hydroxide layers of the newly forming precipitate phase, causing a decrease of the Ni-O distances and, in turn, an increase of the crystal-field splitting energy. Comparison with Ni model compounds showed that the band at 14,900 cm−1 is a unique fingerprint of α-Ni(OH)2, and the band at 15,300 cm−1 of Ni-Al LDH. Although the complete transformation of α-Ni(OH)2 into a Ni phyllosilicate causes a significant contraction of the Ni hydroxide sheet as indicated by band positions intermediate to those of α-Ni(OH)2 and Ni-Al LDH, incipient states of silication do not influence Ni-O distances and cannot be detected by DRS. The first evidence for the formation of a precipitate was obtained after 5 min (pyrophyllite), 7 hr (talc), 24 hr (gibbsite), and 3 days (amorphous silica). For both pyrophyllite and talc, where sufficiently long time series were available, the ν2 energy slightly increased as long as the Ni uptake from solution continued (3 days for pyrophyllite, 30 days for talc). This may be explained by a relative decrease of relaxed surface sites due to the growth of crystallites. Our study shows that the formation of both α-Ni(OH)2 and Ni-Al LDH may effectively decrease aqueous Ni concentrations in soils and sediments. However, Ni-Al LDH seems to be thermodynamically favored when Al is available. 相似文献
5.
The Witwatersrand goldfields contain abundant assemblages that include pyrophyllite, chloritoid, chlorite, kaolinite and/or kyanite, with quartz. A chemographic analysis of the system Fe(Mg)-Al-Si-O-H involving these minerals yields 22 potential phase diagrams. Using orientation criteria and thermodynamic calculations as further constraints, this list has been reduced to three possible diagrams. New thermodynamic data favour one of these in particular.
This chemographic analysis demonstrates that formation of chloritoid is not restricted to the breakdown reaction of kaolinite plus chlorite in the F(M)ASH system, as stated by previous studies, but could be from pyrophyllite + chlorite → chloritoid + quartz + H2 O.
The metamorphic temperature variation between Witwatersrand goldfields exceeded 65 C, based on chlorite and chloritoid compositions. The lower and upper pressure limits are constrained by the andalusite to kyanite, and the sudoite/chlorite to carpholite boundaries, i.e. 1.5–2.8, and 7 kbar, respectively. The widespread pyrophyllite, chlorite and Fe-chloritoid in all the Witwatersrand goldfields, and the local occurrence of sudoite indicate a consistent low-pressure environment in which Mg-chloritoid would not be stable. 相似文献
This chemographic analysis demonstrates that formation of chloritoid is not restricted to the breakdown reaction of kaolinite plus chlorite in the F(M)ASH system, as stated by previous studies, but could be from pyrophyllite + chlorite → chloritoid + quartz + H
The metamorphic temperature variation between Witwatersrand goldfields exceeded 65 C, based on chlorite and chloritoid compositions. The lower and upper pressure limits are constrained by the andalusite to kyanite, and the sudoite/chlorite to carpholite boundaries, i.e. 1.5–2.8, and 7 kbar, respectively. The widespread pyrophyllite, chlorite and Fe-chloritoid in all the Witwatersrand goldfields, and the local occurrence of sudoite indicate a consistent low-pressure environment in which Mg-chloritoid would not be stable. 相似文献
6.
The hydroxyl stretching frequencies of four phyllosilicates have been measured at high pressures and temperatures using an externally heated diamond-anvil cell and synchrotron infrared spectroscopy. Spectra were measured up to 26, 31, 21 and 8 GPa at room temperature for samples of talc, pyrophyllite, muscovite and 10-Å phase, respectively. Spectra were also measured in the range 273–500 K at ambient pressure for all samples and at 8–9 GPa for talc and pyrophyllite. The frequency of the Mg3OH band in talc increases with pressure due to the absence of hydrogen bonding. The different orientation of the hydroxyl group in pyrophyllite and muscovite leads to hydrogen bonding and a decrease in the frequency of the Al2OH band with pressure. 10-Å phase is approximately equivalent to talc with the addition of interlayer H2O. In a spectrum of a sample synthesised for 143 h, two hydroxyl stretching bands are clearly resolved on compression. One is the same as the Mg3OH band in talc, indicating the presence of intra-layer hydroxyl in a talc-like environment with no hydrogen bonding. The other, which separates from the talc-like band at 1 GPa, is associated with intra-layer hydroxyl that is hydrogen bonded to interlayer H2O. There are equivalent bands in high-pressure spectra of a sample of deuterated 10-Å phase, synthesised for 400 h. This sample shows a greater extent of hydrogen bonding at ambient pressure than the 143 h sample. For all of the phases studied, increasing temperature leads to a decrease in frequency for every hydroxyl stretching vibration, both at low and high pressures. The shifts in frequency with temperature are an order of magnitude greater than the shifts with pressure when normalised to previously measured structural parameters. 相似文献
7.
Tetsuichi TAKAGI Sang–Mo KOH Moon–Young KIM Kazuki NAITO Sadahisa SUDO 《Resource Geology》2000,50(4):243-256
Abstract: The Milyang pyrophyllite deposit, which is embedded in the Late Cretaceous Yuchon Group of the Kyongsang Supergroup, is one of the largest hydrothermal clay deposits in the Kyongsang basin, southeast Korea. Host rocks of the deposit are porphyritic andesite lava and minor andesitic lapilli tuff. In the Milyang district, a hydrothermally altered zone is about 2 × 3 km in extent; we can recognize the concentric arrangement of advanced argillic, propylitic, and sericitic alteration zones from the central to peripheral parts of the zone. The Milyang pyrophyllite deposit forms a part of the advanced argillic alteration zone. The Milyang pyrophyllite deposit is subdivided into the following four zones based on mineral assemblages: the pyrophyllite zones 1, 2, 3, and the silicified zone. The pyrophyllite zone 1, which occupies the central part of the deposit, comprises mainly pyrophyllite, kaolinite, and diaspore without quartz. Diaspore nodules often concentrate in beds 40–50 cm thick. Andalusite, dumortierite, and tourmaline locally occur as network veins, crack‐filler, or small spherulitic spots. The Al2O3 content of the ore ranges from 27 to 36 wt%. The pyrophyllite zone 2, which constitutes a major part of the deposit, comprises mainly pyrophyllite, kaolinite, and quartz. The Al2O3 content of the ore ranges from 15 to 24 wt%. The pyro‐phyllite zone 3 is the hematite‐rich marginal facies of the deposit. The silicified zone, which occurs as beds and septa, is mostly composed of quartz with minor pyrophyllite and kaolinite; the SiO2 contents range from 79 to 90 wt%. Comparing chemical compositions of the high‐Al ores with those of unaltered host andesite, the Fe, Ca, alkalis, HFSE, and HREE contents are significantly depleted, whereas S, B, As, Sr, and LREE are enriched. The hydrothermal alteration of the Milyang pyrophyllite deposit can be classified into the following four stages: 1) extensive sericitic and propylitic alteration, 2) medium‐temperature (200–250°C) advanced argillic alteration, 3) high‐temperature (250–350°C or more) advanced argillic alteration, and 4) retrograde low‐temperature alteration. The heat and some volatile components such as B and S would be derived from the Pulguksa Granite intruded underneath the deposit. 相似文献
8.
G.N. PHILLIPS 《Journal of Metamorphic Geology》1988,6(3):311-332
Abstract Chloritoid and pyrophyllite occur together in all major goldfields of the Witwatersrand Basin and are widespread in virtually all rock types of the upper Witwatersrand Supergroup, including metaconglomeratic reefs and altered mafic rocks. Both minerals are particularly characteristic of the pelitic horizons intimately associated with reef packages, but they are also developed locally in the regionally persistent metapelites that have basin-wide extent. Pyrophyllite is particularly common in foliated zones, adjacent to quartz veins, and near unconformably overlying auriferous conglomerates. The wide distribution of chloritoid and pyrophyllite in metapelites of the Witwatersrand Basin is attributed to alteration of chlorite-rich shales, rather than to unusual premetamorphic starting materials. This alteration event involved the redistribution of many elements, with up to 40% volume loss, mainly due to removal of silica. Removal of most of the Mg and some Fe accounts for the stabilization of chloritoid and pyrophyllite. Relatively immobile elements included Al, Ti, Nb, Cr, V, P, La and Ce, whereas Si, Fe, Mn, Zn, Co, Ni, Cu, Mg and Ca were lost, and K, Rb and Ba were introduced by an infiltrating fluid. The alteration event is inferred to have been within the chloritoid and pyrophyllite stability field (and thus syn-metamorphic) as bulk chemical changes in metapelites are from chlorite directly towards chloritoid and then pyrophyllite, rather than to lower grade minerals such as kaolinite. Muscovite–chlorite–chloritoid and muscovite–chloritoid–pyrophyllite assemblages are attributed to fluid buffering along appropriate curves, as their production by metamorphism of lower grade mineral mixes is considered unlikely, based on the present bulk rock compositional data. A metamorphic timing for the alteration accounts for the correlation of strongly foliated areas with greater degrees of inferred alteration. The transitions from chlorite to chloritoid to pyrophyllite define zones of increasing alteration. Widespread infiltration as part of peak metamorphism is suggested by the distribution of chloritoid and pyrophyllite, quartz veining and textures. Fluid:rock ratios calculated from a silica budget in one metapelitic horizon exceed 100:1 over many square kilometres. These values need not imply multi-pass fluid flow, as much of the silica migration may be redistribution on a scale of a few metres, from source rocks into veins. Although infiltration during metamorphism may have affected much of the upper Witwatersrand succession, channelized fluid flow within reef packages, along faults and unconformities and in certain metaconglomerates and metapelites is inferred. 相似文献
9.
Holger Kulke 《Contributions to Mineralogy and Petrology》1969,20(2):135-163
The “Stubensandstein” (Middle Keuper) of the Memmingen region (Southern Germany) — the detrital deposit of a nearby granitic red-soil area — was investigated sedimentologically, on the basis of three cores from 2,230, 1,930 and 1,420 metres depth. Shale- and marl-layers are intercalated in beds of coarse grained, immature sandstone. The rare carbonate is predominantly early diagenetic dolomite. The most exceptional result of the diagenesis is the formation of a variously composed claymineral association in the porous sandstones: Kaolinite, sudoite, sudoite/montmorillonitemixed-layers and tosudite (a regular 1∶1 sudoite/montm.-mixed-layer). The detrital component of the clay-minerals (illite and illite/montm.-mixed-layers) is preserved more or less unchanged in the shales, marls and argillaceous sandstones. Two main diagenetic phases can be distinguished:
- The early diagenetic formation of kaolinite out of the solution-products of feldspars in acid environment. Quartz is precipitated in microcrystalline form in the pore space, garnet is partly dissolved.
- In the course of the Neogen deep burial stage kaolinite becomes unstable and sudoite and sudoite/montm. are newformed; the intensity of this phenomenon depends on depth of burial and rock-permeability. Calcite sporadically crystallizes out of an environment that has become alkaline; adjacent feldspar becomes more or less dissolved and is pseudomorphically replaced by calcite. Al(OH)3 is thereby released and is fixed in montmorillonite, thus forming the sudoite of the carbonatic horizons, which never contain kaolinite.
10.
Élisa Morichon Thierry Allard Daniel Beaufort David Quirt 《Physics and Chemistry of Minerals》2010,37(3):145-152
Natural radiation-induced defects were identified in specimens of sudoite (Al–Mg di-trioctahedral chlorite) related to unconformity-type
uranium deposits at the base of the Athabasca Group (Saskatchewan, Canada), using electron paramagnetic resonance (EPR) spectroscopy
at X- and Q-band frequencies. X-band spectra indicate the presence of a main native defect, named the As-center, whose EPR signal is dominated by an axially distorted spectrum with apparent principal components as follows: g
// = 2,051 and g
⊥ = 2,005, and a secondary defect with apparent component g = 2,025. The study of oriented specimens shows that the main defect has its g
// component perpendicular to the (ab) plane of sudoite. The As-center corresponds to an electron hole located on oxygen atoms of the structure and is likely associated with Si, according
to the lack of hyperfine structure. The As-center in sudoite has EPR parameters similar to the A-center in kaolinite and dickite, and the Ai-center in illite. The saturation behavior of EPR spectra as a function of power demonstrates that native defects of sudoite
are different from those known in other clays, such as kaolinite, dickite or smectite, but are similar to those of illite.
The isochronal annealing data suggest that the main defect in sudoite is stable to more than 300°C. The corresponding defects
characterized in sudoite may have the potential for tracing past radionuclide migration around unconformity-type uranium deposits. 相似文献
11.
Thomas D. Hoisch 《Contributions to Mineralogy and Petrology》1991,108(1-2):43-54
Interaction parameters derived using empirical calibration methods indicate strong non-ideality in the mixing of octahedrally-coordinated
cations in muscovite and biotite. The data set used for calibration comprises mineral compositions from 49 samples containing
quartz, muscovite, biotite, garnet, plagioclase and Al2SiO5 (kyanite or sillimanite). Pressures and temperatures in the data set were determined through the simultaneous application
of geothermometry based on the garnet-biotite FeMg1 exchange equilibrium and geobarometry based on the anorthite-breakdown equilibrium. Two equilibria yielded simple expressions
from which binary interaction parameters for octahedrally-coordinated cations in biotite could be directly determined. A four-component
(Fe2+, Mg, Al, Ti) regular symmetric mixing model was assumed for biotite. One equilibrium yielded a simple expression from which
an interaction parameter for the mixing of the MgAl-celadonite component in muscovite could be directly determined. Two sets
of calculations were performed utilizing different calibrations of the garnet-biotite geothermometer and the anothite-breakdown
geobarometer and different garnet activity models. Both placed samples within or near the stability field of the Al2SiO5 phase present in each sample and both yielded similar values for the interaction parameters within narrow uncertainties,
indicating that the values are insensitive to differences in the underlying methods. Using the derived interaction parameters,
activity models were formulated for the annite, phlogopite, eastonite, and siderophyllite components of biotite, and for the
MgAl-celadonite component of muscovite. These were utilized for the empirical calibration of 45 fluid-independent equilibria
involving unique combinations of phase components from the mineral assemblage garnet + plagioclase±biotite±muscovite±quartz.
Forty-three of the equilibria may be applied as geobarometers to equilibrium assemblages of quartz + muscovite + biotite +
garnet + plagioclase when care is taken to insure that applications are restricted to valid compositional ranges. For these,
the calibrations yielded multiple correlation coefficients ranging from 0.953 to 0.998 and standard deviations of the residuals
ranging from 597 to 118 bars. 相似文献
12.
In the Pötürge (Malatya, Turkey) area pyrophyllite occurrences are common in the shear zones, mostly in the form of lenses along faults. Mineralogical investigations (XRD, FTIR and SEM) revealed that pyrophyllite, kaolinite (dickite) and quartz are present in the form of major phases and muscovite (sericite), kyanite, chlorite, and alunite are only present in the form of minor phases. This study revealed that the existence of the kyanite phase points out to high pressure and temperature conditions which the rocks were underwent. On the other hand, the minerals such as pyrophyllite, kaolinite, and alunite are products of a low degree metamorphism (retrograde). The mineral paragenesis in the pyrophyllite deposits suggests that the formation of minerals took place in two ways: (1) the transformation of kyanite into pyrophyllite and quartz through retrograde metamorphism by a high degree temperature, (2) then pyrophyllite and probably muscovite were transformed into kaolinite and alunite through reactions with relatively low temperature hydrothermal fluids. The geochemical data indicate that during the retrograde metamorphism the elements K, Rb, Sr, Ba, S, and Fe were mobile, the elements Si, Al, P moderately mobile to immobile and the HPS elements (Zr, Ti, and Nb) were immobile. It was shown that the formation of pyrophyllite, kaolinite and alunite was associated with depletion in alkalis, Mg, Fe and enrichment of elements including Sr, Ba, and S. Mineralogical and geochemical data suggest that parent rocks (pre-metamorphism) of the Pötürge pyrophyllite were probably kaolinite, Al-rich clays or bauxites. 相似文献
13.
R. P. Wintsch 《Contributions to Mineralogy and Petrology》1980,73(4):421-428
A pE-pH diagram for supercritical aqueous fluids at 500° C and 2 kb total pressure is calculated from thermodynamic data assuming ideal mixing of gas species. The experimental data on the stability of annite-phlogopite solid-solutions (Wones and Eugster 1965) and on the stability of aluminous biotite (Rutherford 1968) have been used to calculate the stability of these biotite solid solutions in sanidine, muscovite and Al2SiO5 bearing assemblages. The resulting pE-pH diagrams show that Al increases the stability field of annite more per atom than does Mg. However, the addition of Al to biotite does not increase the stability of annite in very acid and alkaline solutions. Environments sufficiently acid to render aluminous biotite metastable are probably not found in nature, but the mildly alkaline environments are attainable. At constant f
O
2, f
H
2 and
the Al content of biotite is at a minimum in muscovite + sanidine bearing assemblages, and increases relatively rapidly with increases in pH in the sanidine field, and increases more slowly with decreases in pH through the muscovite and Al2SiO5 fields.These diagrams show that the composition of biotite solid-solutions containing more aluminum than ideal annite-phlogopite and coexisting with sanidine and magnetite cannot be used to infer intensive parameters (T
f
O
2,
) prevailing during the crystallization of the biotite, and that in no case can any biotite composition in muscovite or Al2SiO5 bearing assemblages be used to extract this information. 相似文献
14.
《International Geology Review》2012,54(4):353-367
Metasedimentary and sedimentary rocks that represent the allochthonous Bolkardagi Unit crop out in the Central Taurus Belt. Devonian units include mainly slate, metadolomite, metadolomitic limestone, and metasandstone. Slates with slaty cleavage and chlorite-mica stacks are characterized by phyllosilicate, quartz, calcite, dolomite, feldspar, and goethite. Phyllosilicates consist of 2M1 and lesser amounts of 1M muscovite, IIb chlorite, pyrophyllite, paragonite. PM, C-V, C-S. rectorite, and dickite, and reflect conditions of the low epizone-anchizone. In the Carboniferous-Triassic units, limestone, clayey limestone, dolomitic limestone, marl, shale, and sandstone retaining primary textures are composed of calcite, dolomite, quartz,1Md illite, chlorite, and I-S, and locally smaller quantities of 2M1 muscovite, PM, paragonite, pyrophyllite, and rectorite. In contrast, the Triassic formation is made up of calcite, 1Md illite, I-S, kaolinite, smectite, chlorite, C-S, C-V, dolomite, and quartz. Textural and mineralogical data indicate that development of the diagenetic-metamorphic grade in the Central Taurus was related to sedimentary burial and thrusting; moreover, the metasedimentary rocks were metamorphosed in a typical anticlockwise P-T-t pathway in an extensional setting. 相似文献
15.
Abstract Microprobe analyses of feldspars in granite mylonites containing flame perthite give compositions that invariably plot as three distinct clusters on a ternary feldspar diagram: orthoclase (Or92–97), albite and oligoclase-andesine. The albite occurs as grains in the matrix, as flame-shaped lamellae in orthoclase, and in patches within plagioclase grains. We present a metamorphic model for albite flame growth in the K-feldspar in these rocks that is related to reactions in plagioclase, rather than alkali feldspar exsolution. Flame growth is attributed to replacement and results from a combination of two retrograde reactions and one exchange reaction under greenschist facies conditions. Reaction 1 is a continuous or discontinuous (across the peristerite solvus) reaction in plagioclase, in which the An component forms epidote or zoisite. Most of the albite component liberated by Reaction 1 stays to form albite in the host plagioclase, but some Na migrates to form the flames within the K-feldspar. Reaction 2 is the exchange of K for Na in K-feldspar. Reaction 3 is the retrograde formation of muscovite (as ‘sericite’) and has all of the chemical components of a hydration reaction of K-feldspar. The Si and Al made available in the plagioclase from Reaction 1 are combined with the K liberated from the K-feldspar, to produce muscovite in Reaction 3. The muscovite forms in the plagioclase, rather than the K-feldspar, as a result of the greater mobility of K relative to Al. The composition of the albite flames is controlled by both the peristerite and the alkali feldspar miscibility gaps and depends on the position of these solvi at the pressure and temperature that existed during the reaction. Using an initial plagioclase composition of An20, the total reaction can be summarized as: 20 oligoclase + 1 K-feldspar + 2 H2O = 2 zoisite + muscovite + 2 quartz + 15 albiteplagioclase+ 1 albiteflame. This model does not require that any additional feldspar framework be accreted at replacement sites: Na and K are the only components that must migrate a significant distance (e.g. from one grain to the next), allowing Al to remain within the altering plagioclase grain. The resulting saussuritization is isovolumetric. The temperature and extent of replacement depends on when, and how much, water infiltrates the rock. The fugacity of the water, and therefore the pressure of the fluid, may have been significantly lower than lithostatic during flame growth. 相似文献
16.
David W. Mohr Robert L. Barnett Joanna Michie 《Contributions to Mineralogy and Petrology》1986,92(3):400-411
A detailed study of retrograde alteration of a staurolite porphyroblast and its surrounding matrix of mica schist has made use of petrographic, modal, and microprobe analysis. Retrogression was to the garnet zone of metamorphism and apparently occurred largely after a temperature decline of 70–100° C. The event caused metasomatic removal of Zn but may have been isochemical relative to other analyzed elements. The best estimate of the overall reaction is: 1 staurolite+3.018 biotite+3.550 quartz+0.629 albite +0.014 anorthite+0.678 NaCl+14.004 H2O =3.274 Na-rich muscovite+3.561 chlorite +0.273 ilmenite+0.110 chloritoid+0.039 garnet +0.339 ZnCl2.Non-systematic variation in composition of analyzed minerals is revealed by statistical treatment of replicate analyses. Such variation involves monovalent and divalent cations within many minerals, but is most pronounced within retrograde muscovite. Muscovite variation involves Si and Al as well as FM and alkalis and does not follow a phengite law of charge-coupled substitution.Relative to the core of the retrograded staurolite crystal, zoning is seen in averaged muscovite compositions and in development of incompatible mineral assemblages, which include chloritoid well within retrograded staurolite but biotite within the matrix. A local gradient in the chemical potential of an Al-bearing component was likely present during retrogression.Alteration of staurolite was probably accomplished by reaction and diffusion through the medium of an intergranular fluid phase. Relative to staurolite, migration of elements involved immigration of considerable amounts of Mg, Na, K, and H and expulsion of Al, Fe, Zn, and O. It is inferred that concentration of Al within the fluid phase was considerably lower than those of monovalent and divalent cations.Preservation of considerable staurolite and evidence for a local concentration gradient of Al in the fluid phase suggest that limited amounts of H2O were available. Expulsion of Zn suggests that much water was not consumed locally but exited the terrane. An attempt at resolution of this dilemna involves fracture-channelized infiltration of H2O into the rock. A more regional petrographic study of retrogression suggests that H2O which entered the rock may have been liberated initially by prograde dehydration at a moderately greater depth of 2–3 km.Results of this study, especially the non-phengitic nature of crystal-chemical substitution within muscovite, indicate chemical reaction under conditions of disequilibrium. Apparently, extent of retrogression was controlled by availability of H2O rather than by thermochemical equilibria. 相似文献
17.
浙江青田单斜晶系叶腊石微结构的高分辨透射电镜研究 总被引：2，自引：2，他引：0
采用X射线粉晶衍射(XRD)、高分辨透射电镜(HR-TEM)及X射线荧光光谱(XRF)对青田叶腊石的矿物学特征进行了较为系统的研究。结果表明:叶腊石矿物颗粒微结构中最基本的构成单元为纳米板片,且该板片多呈聚集态,单层板片面积大小不一,厚度为(8±2)nm。XRF分析结果表明青田叶腊石原矿混合物中SiO2与Al2O3的分子个数比为6.2,明显高于纯叶腊石中SiO2与Al2O3的分子个数比4.0。HR-TEM对叶腊石晶体结构的研究证实青田叶腊石具有典型的单斜晶系特征,该结论与叶腊石XRD结论一致;且XRD分析结果证实其伴生矿为石英,该结论与XRF所获得的青田叶腊石的"富硅"特征吻合。此外,叶腊石微结构中存在着较明显的晶体缺陷。在高能电子束辐照作用下,叶腊石晶体结构发生明显的破坏,并最终转变为非晶态结构。 相似文献
18.
A quantitative petrogenetic grid for pelitic schists in the system KFMASH that includes the phases garnet, chlorite, biotite,
chloritoid, cordierite, staurolite, talc, kyanite, andalusite, sillimanite, and pyrophyllite (with quartz, H2O and muscovite or K-feldspar in excess) is presented. The grid is based on thermodynamic data of Berman et al. (1985) and
Berman (1988) for endmember KFASH and KMASH equilibria and natural Fe-Mg partitioning for the KFMASH system. Calculation of
P-T slopes and the change in Fe/(Fe+Mg) along reactions in the KFMASH system were made using the Gibbs method. In addition, the
effect on the grid of MnO and CaO is evaluated quantitatively. The resulting grid is consistent with typical Buchan and Barrovian
parageneses at medium to high grades. At low grades, the grid predicts an extensive stability field for the paragenesis chloritoid+biotite
which arises because of the unusual facing of the reaction chloritoid+biotite + quartz+H2O = garnet+chlorite+muscovite, which proceeds to the right with increasing T in the KFMASH system. However, the reaction proceeds to the left with increasing T in the MnKFASH system so the assemblage chloritoid + biotite is restricted to bulk compositions with high Fe/(Fe+Mg+Mn).
Typical metapelites will therefore contain garnet+chlorite at low grades rather than chloritoid + biotite. 相似文献
19.
叶蜡石化蚀变过程中的元素活动性与流体性质:以山西五台地区白云叶蜡石矿为例 总被引：1，自引：0，他引：1
热液蚀变过程中的元素活动性与流体性质对深入理解矿物稳定性和成矿作用具有重要的意义。本文以华北克拉通中北部山西五台地区的白云叶蜡石矿为例,研究了蚀变过程中元素迁移特征和流体性质。该矿体围岩以绿片岩相酸性火山岩为主,岩性为绢云钠长石英片岩并夹有少量的绿泥钠长片岩。矿区内蚀变分带明显,可分为早期的黄铁绢英岩化(绢云母-石英-黄铁矿)和晚期叠加的叶蜡石化(叶蜡石-伊利石-高岭石-石英),而金矿化则主要发育于黄铁绢英岩化带内。Log fo2-pH相图模拟结果显示,早期黄铁绢云岩化蚀变热液具有弱酸性至偏中性(pH=5.24~5.87)和较低氧逸度(位于黄铁矿+黄铜矿稳定相区内)特征;而引起叶蜡石化蚀变的热液具有强酸性(pH=2.07~2.20)和高氧逸度(位于HM缓冲线以上)特征。质量平衡迁移分析结果显示,随着叶蜡石化蚀变作用的增强,叶蜡石矿石中的Al2O3行为较稳定,SiO2、Na2O和K2O含量相对于围岩绢云钠长石英片岩呈不同程度的迁入,而其余氧化物大量活化迁出。微量元素Nb、Ta、Th、U、Rb和Ga含量相对升高,Th/U比值略有升高;Sr、Ba、Zr、Hf明显亏损,Zr/Hf比值从34~41下降到17~22。稀土元素均发生一定程度的活化迁移,且轻稀土迁出程度更高。Y/Ho比值(28~32)高于球粒陨石的Y/Ho(26~28),表明Y-Ho在叶蜡石化蚀变过程中表现出不同的地球化学行为。Eu负异常明显增大,这可能与长石的分解关系密切。围岩绢云钠长石英片岩中金属元素含量较高且Au与As含量之间呈明显正相关性,但在叶蜡石矿石中大部分金属元素含量均低于检出限,说明金属元素在叶蜡石化蚀变作用过程中发生了强烈的活化迁移,这与岩相学上叶蜡石矿石中可见港湾状细粒赤铁矿而缺乏黄铁矿的特征吻合。本文研究结果表明叶蜡石化过程中,大量的所谓不活动元素(如P、Ti、Zr、Hf、Y和Ho等)发生了显著迁移并导致Zr/Hf和Y/Ho比值的解耦,并伴随着大量金属元素的迁出,说明叶蜡石化不利于金矿化的形成。 相似文献
20.
Hydrothermal alteration of a quartz‐K‐feldspar rock is simulated numerically by coupling fluid flow and chemical reactions. Introduction of CO2 gas generates an acidic fluid and produces secondary quartz, muscovite and/or pyrophyllite at constant temperature and pressure of 300°C and 200 MPa. The precipitation and/or dissolution of the secondary minerals is controlled by either mass‐action relations or rate laws. In our simulations the mass of the primary elements are conserved and the mass‐balance equations are solved sequentially using an implicit scheme in a finite‐element code. The pore‐fluid velocity is assumed to be constant. The change of rock volume due to the dissolution or precipitation of the minerals, which is directly related to their molar volume, is taken into account. Feedback into the rock porosity and the reaction rates is included in the model. The model produces zones of pyrophyllite quartz and muscovite due to the dissolution of K‐feldspar. Our model simulates, in a simplified way, the acid‐induced alteration assemblages observed in various guises in many significant mineral deposits. The particular aluminosilicate minerals produced in these experiments are associated with the gold deposits of the Witwatersrand Basin. 相似文献