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1.
The phase transition between the
and
phases of anorthite has been studied at elevated pressure by single-crystal X-ray diffraction in a diamond-anvil cell. The
phase transition is shown to be first-order in character for both end-member anorthite (CaAl2Si2O8) and for an anorthite with a small amount of albite component (NaAlSi3O8) in solid solution. Reversals of the transition across the phase boundary at three other compositions show that the transition
pressure (P
Tr) increases with increasing albite content. This behaviour is compared with that observed at elevated temperatures, and is
analysed in terms of Landau theory. 相似文献
2.
Electron diffraction and electron microscopic evidence is presented for a dynamical and reversible
phase transition in anorthite at T
c=516 K. Antiphase boundaries with a displacement vector, R=1/2[111] become unstable at T
c, while other antiphase boundary loops with the same displacement vector are formed. These interfaces are very mobile and vibrate with a frequency which increases strongly with temperature. At temperatures considerably above T
c, a shimmering effect is observed on imaging in dark field using diffuse c reflections. These observations are in agreement with the interpretation of the high temperature body-centered phase as a statistical dynamical average of very small c type antiphase domains of primitive anorthite. We propose that the c type antiphase domains in primitive anorthite originate from ordered and anti-ordered configurations around Ca2+ ions at (ooo) and (oio) [likewise (zoo) and (zio)] positions. The dynamical model for the transition involves a two-stage mechanism: a softmode mechanism causing the aluminosilicate framework to approach body-centered symmetry, followed by an orderdisorder of the Ca2+ ion configurations. Close to T
c, statistical fluctuations set in and breathing motion type lattice vibrations of the aluminosilicate framework cause the configurations around Ca (ooo) and Ca(oio) [likewise Ca(zoo) and Ca(zio)] in the
configuration to dynamically interchange through an intermediate
configuration. The dynamical nature of the phase transition in anorthite is comparable to the — phase transition in quartz. 相似文献
3.
The oxygen fugacity (
) of a C-O-H fluid in equilibrium with graphite has been determined in the range 10–30 kbar by equilibrating solid
-buffer assemblages in graphite capsules containing C-O-H fluid. By using different buffers (FexO-Fe3O4, Ni-NiO, Co-CoO, Mo-MoO2), the
of the graphite-saturated fluid is bracketed within a narrow range. This technique produces a calibration for the
imposed on a sample contained within a graphite capsule. To achieve a thermodynamically-invariant system at fixed P and T,
the
was imposed on the system with an external buffer and the double-capsule technique. The experiments were performed in solid-media,
high pressure apparatus with 19 mm tale-pyrex assemblies. A series of experiments at 10, 15, 20, 25, and 30 kbar, 800–1600°
C, with
imposed by the Fe2O3-Fe3O4-H2O equilibrium were conducted. The experimental results have been fitted to the following equation:
|
相似文献
4.
Chang-Jo F. Chung 《Mathematical Geology》1993,25(7):851-865
Multivariate statistical analyses have been extensively applied to geochemical measurements to analyze and aid interpretation of the data. Estimation of the covariance matrix of multivariate observations is the first task in multivariate analysis. However, geochemical data for the rare elements, especially Ag, Au, and platinum-group elements, usually contain observations the below detection limits. In particular, Instrumental Neutron Activation Analysis (INAA) for the rare elements produces multilevel and possibly extremely high detection limits depending on the sample weight. Traditionally, in applying multivariate analysis to such incomplete data, the observations below detection limits are first substituted, for example, each observation below the detection limit is replaced by a certain percentage of that limit, and then the standard statistical computer packages or techniques are used to obtain the analysis of the data. If a number of samples with observations below detection limits is small, or the detection limits are relatively near zero, the results may be reasonable and most geological interpretations or conclusions are probably valid. In this paper, a new method is proposed to estimate the covariance matrix from a dataset containing observations below multilevel detection limits by using the marginal maximum likelihood estimation (MMLE) method. For each pair of variables, sayY andZ whose observations containing below detection limits, the proposed method consists of three steps: (i) for each variable separately obtaining the marginal MLE for the means and the variances,
,
,
, and
forY andZ: (ii) defining new variables by
and
and lettingA=C+D andB=C–D, and obtaining MLE for variances,
and
forA andB; (iii) estimating the correlation coefficient YZ by
and the covariance
YZ
by
. The procedure is illustrated by using a precious metal geochemical data set from the Fox River Sill, Manitoba, Canada. 相似文献
5.
Single crystal Raman spectra of pyrite-type RuS2, RuSe2, OsS2, OsSe2, PtP2, and PtAs2 are presented and discussed with reference to the energies of the X-X stretching modes
x-x (A
g, F
g) and the X2 librations
(E, 2Fg). The main results obtained are (i) strong Raman resonance effects, (ii) different sequences for
x-x (A
g) and
(E
g), i.e.,
R_{x_2 } $$
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for PtP2 and PtAs2 and
R_{x_2 } $$
" align="middle" border="0">
for OsS2, owing to the interplay of intraionic and interionic lattice forces, (iii) greater strengths for the intraionic P-P and As-As bonds compared to the S-S and Se-Se bonds, respectively, and (iv) a strong influegnce of the metal ions on the strength of the X-X bonds.This is contribution LXI of a series of papers on lattice vibration spectra 相似文献
6.
Titania, TiO2, precipitation in natural blue sapphire (Fe, Ti: -Al2O3) has been investigated using high resolution and analytical transmission electron microscopy. The structure and habit of the TiO2 precipitate depends on both the Ti4+ concentration and the temperature at which the precipitate formed. Tetragonal TiO2 (Rutile) grows at 1350° C but at 1150° C an orthorhombic non-equilibrium TiO2 polymorph precipitates. Both TiO2 polymorphs nucleate in the (0001)s plane as lens shaped discs twinned along their diameter. The crystallographic alignment of each type of TiO2 precipitate with respect to the -Al2O3 host matrix provides a high degree of structural coherency with minimal lattice mismatch. Electron diffraction analysis established the following precipitate/host orientation relationships: tetragonal TiO2: {011}r {11
07B;100}r(0001)s and 01
r10
0s twinned along the (011)r planeand orthorhombic TiO2: {021}{11
0}s, {100}(0001)s and 0
2 10
0s twinned along the (021) plane. 相似文献
7.
Zusammenfassung Die chemische Analyse des neuen Minerals Johillerit mit der Elektronenmikrosonde ergab: Na2O 5,4, MgO 18,3, ZnO 5,4, CuO 15,8 und As2O5 55,8, Summe 100.7%. Aus diesem Ergebnis wurde die idealisierte Formel Na(Mg, Zn)3 Cu(AsO4)3 abgeleitet. Johillerit ist monoklin mit der RaumgruppeC2/c. Die Gitterkonstanten sind:a=11,870 (3),b=12,755 (3),c=6,770 (2) , =113,42 (2)°,Z=4. Die stärksten Linien des Pulverdiagramms sind: 4,06 (5) (22
), 3,50 (4) (310), 3,25 (8) (11
), 2,75 (10) (330, 240), 2,64 (5) (311, 13
, 40
), 1,952 (4) (13
, 35
), 1,682 (4) (20
, 460), 1,660 (5) (40
, 71
, 550, 64
), 1,522 (4) (442, 153, 13
). Es bestehen enge strukturelle Beziehungen zwischen Johillerit und O'Danielit, Na(Zn, Mg)3H2(AsO4)3, sowie einigen synthetischen. Verbindungen.Johillerit ist violett durchscheinend. Die Spaltbarkeit nach {010} ist ausgezeichnet und nach {100} und {001} gut.H (Mohs)3.D=4,15 undD
X
=4,21 g·cm–3. Das Mineral ist optisch zweiachsig positiv, 2V80 (5)°. Die Werte der Lichtbrechung sindn
=1,715 (4),n
=1,743 (4) undn
=1,783 (4). Die Auslöschung istn
b und auf (010)n
c16°. Johillerit ist stark pleochroitisch mit den AchsenfarbenX=violett-rot,Y = blauviolett undZ = grünblau. Das neue Mineral kommt in radialstrahligen Massen gemeinsam mit kupferhaltigem Adamin und Konichalcit in zersetzem Kupfererz von Tsumeb, Namibia, vor. Die Benennung erfolgte nach Prof. Dr.J.-E. Hiller (1911–1972).
Johillerite, Na(Mg, Zn) 3 Cu(AsO 4 ) 3 , a new mineral from Tsumeb, Namibia Summary Electron microprobe analysis of the new mineral johillerite gave Na2O 5.4, MgO 18.3, ZnO 5.4, CuO 15.8, and As2O5 55.8, total 100.7%. From this result, the ideal formula is given as Na(Mg, Zn)3 Cu(AsO4)3. Johillerite crystallizes monoclinic,C2/c. The unit cell dimensions are:a=11.870(3),b=12.755 (3),c=6.770 (2) , =113.42 (2)°,Z=4. The strongest lines on the X-ray powder diffraction pattern are: 4,06 (5) (22 ), 3,50 (4) (310), 3,25 (8) (11 ), 2,75 (10) (330, 240), 2,64 (5) (311, 13 , 40 ), 1,952 (4) (13 , 35 ), 1,682 (4) (20 , 460), 1,660 (5) (40 , 71 , 550, 64 ), 1,522 (4) (442, 153, 13 ). There is a close relationship between johillerite, o'danielite, Na(Zn, Mg)3H2(AsO4)3, and some synthetic compounds. Johillerite is violet in colour, transparent. Cleavage is {010} perfect, {100} and {001} good.H (Mohs)3.D=4.15 andD X =4.21 g·cm–3. The mineral is optically biaxial positive, 2V80 (5)°. The refractive indices are:n =1.715 (4),n =1.743 (4),n =1.783 (4). The extinction isn b and on (010)n c16°. Strongly pleochroic with axial coloursX=violet-red,Y=bluish violet andZ=greenish blue. The new mineral was found in radiated masses together with cuprian adamite and conichalcite in an oxidized copper ore from Tsumeb, Namibia. It is named in honour of Prof. Dr.J.-E. Hiller (1911–1972). Mit 1 Abbildung 相似文献 8.
To investigate the point defect chemistry and the kinetic properties of manganese olivine Mn2SiO4, electrical conductivity () of single crystals was measured along either the [100] or the [010] direction. The experiments were carried out at temperatures T=850–1200 °C and oxygen fugacities
atm under both Mn oxide (MO) buffered and MnSiO3 (MS) buffered conditions. Under the same thermodynamic conditions, charge transport along [100] is 2.5–3.0 times faster than along [010]. At high oxygen fugacities, the electrical conductivity of samples buffered against MS is 1.6 times larger than that of samples buffered against MO; while at low oxygen fugacities, the electrical conductivity is nearly identical for the two buffer cases. The dependencies of electrical conductivity on oxygen fugacity and temperature are essentially the same for conduction along the [100] and [010] directions, as well as for samples coexisting with a solid-state buffer of either MO or MS. Hence, it is proposed that the same conduction mechanisms operate for samples of either orientation in contact with either solid-state buffer.The electrical conductivity data lie on concave upward curves on a log-log plot of vs
, giving rise to two
regimes with different oxygen fugacity exponents. In the low-
regime
, the
exponent, m, is 0, the MnSiO3-activity exponent, q, is 0, and the activation energy, Q, is 45 kJ/mol. In the high
regime
10^{ - 7} {\text{atm}}} \right)$$
" align="middle" border="0">
, m=1/6, q=1/4–1/3, and Q=45 and 200 kJ/mol for T<1100 °c=" and=">T>1100 °C, respectively. 相似文献
9.
Zusammenfassung Colquiriit tritt in Vergesellschaftung mit Ralstonit, Gearksutit, Zinkblende, Madocit und Pyrit im Bereich der Zinnlagerstätte von Colquiri in Bolivien auf. Das als selten zu betrachtende Mineral bildet maximal cm-große xenomorphe durchscheinende bis durch-sichtige Körner von weißlicher Farbe. Es zeigt keine Spaltbarkeit. Härte ca. 4; Dichte (gem.) 2,94, (ber.) 2,95 g/cm3;n
1,385±0.002,n
1,388±0,002, einachsig oder schwach zweiachsig, negativ. Colquiriit kristallisiert trigonal, Raumgruppe
oderP31c,a
0 5,02,c
0 9,67 Å,Z=2. Stärkste Linien des Pulverdiagramms: 3,98(7)
; 3,23(10)
; 2,22(9)
; 1,736(8)
. Eine chemische Analyse ergab: Li 3,1, Na 0,34, Mg 0,55, Ca 22,8, Al 13,4, F 58,0, Gewichtsverlust (105 °C) 0,5, Summe 98,69%, woraus sich die idealisierte Formel LiCaAlF6 ableiten läßt. Beim Erhitzen wird das Gitter zwischen 800 und 900°C zerstört.
Colquiriite, a new fluoride mineral from the Colquiri tin deposit in Bolivia Summary Colquiriite occurs at the Colquiri tin deposit in Bolivia and is associated with ralstonite, gearksutite, sphalerite, madocite and pyrite. The mineral, which probably is a rare species, forms anhedral translucent to transparent white grains reaching up to 1 cm in size. No cleavage; hardness about 4; density (meas.) 2.94, density (calc.) 2.95 g/cm3;n 1.385±0.002,n 1.388±0.002, uniaxial or weakly biaxial, negative. Colquiriite is trigonal,a 0 5.02,c 0 9.67 Å, space group orP31c,Z=2. The strongest lines of the powder pattern are: 3.98(7) ; 3.23(10) ; 2.22(9) ; 1.736(8) . The chemical analysis gave: Li 3.1, Na 0.34, Mg 0.55, Ca 22.8, Al 13.4, F 58.0, weight loss (105 °C) 0.5, sum 98.69%, leading to the idealized formula LiCaAlF6. Heating experiments show that the lattice breaks down between 800 and 900 °C. The new mineral and its name have been approved by the I.M.A. Commission on New Minerals and Mineral Names.相似文献 10.
Zusammenfassung Die Gefüge von Pyrrhotinerzen von vier Lagerstätten wurden mit einem Röntgentexturgoniometer untersucht. Alle Proben zeigen eine Einregelung von (0001) ± parallel zur Ebene der Lagigkeit (s) der Erze. Die Gefügediagramme der (10
2)-, (11
0)- und (10
0)-Reflexe von drei Fundpunkten haben orthorhombische Symmetrie. Die gleichen Diagramme der vierten Lagerstätte sind hexagonal.Die orthorhombischen Gefüge werden durch eine Deformation mit einfacher Scherung erklärt. Mit Hilfe eines Rechenprogrammes wurden entsprechende synthetische Gefügediagramme erzeugt. Ihre Ähnlichkeit mit der Mehrzahl der natürlichen Texturen macht das angenommene Modell wahrscheinlich. Auch kann geschlossen werden, daß die Proben — ausgenommen diejenigen mit nicht hinreichend deutbarer hexagonaler Symmetrie — durch eine Scherverformung entstanden sind.Gelegentlich scheint es möglich, durch Gefügeuntersuchungen an Erzen Rückschlüsse auf die tektonische Geschichte der Lagerstätte bzw. auf deren Beanspruchung zu ziehen.
The fabrics of pyrrhotite ores from four deposits are determined by means of an X-ray texture goniometer. All specimens show (0001) ± parallel to the plane of schistosity (s) of the ores. The pole figures of the (10 2)-, (11 0)-, and (10 0)-reflections from samples of three localities are of orthorhombic symmetry. The same pole figures from the fourth deposit show hexagonal symmetry.The fabrics of pyrrhotite with orthorhombic symmetry are explained assuming a model with a deformation by simple shear. Synthetic diagrams are plotted using a program which simulates the conditions of this model. The synthetic diagrams are in good agreement with most of the measured ones, and this argues for the validity of the suggested model on the one hand and on the other hand confirms that these pyrrhotite fabrics may have been formed by simple shear. The fabrics with hexagonal symmetry seem to be produced by a quite different mechanism.In some cases one may infer from the results of the fabric analysis of ores to the tectonical history and the mode of deformation of the ore deposit.相似文献 11.
Otto Zedlitz 《Mineralogy and Petrology》1965,10(1-4):130-139
Zusammenfassung Die von Dr.Baumann, Heidelberg, synthetisierten Quarze zeichnen sich nicht nur durch eine außerordentliche Klarheit, sondern auch durch eine auffallende Morphologie aus. Es werden drei grundsätzlich verschiedene Typen beschrieben. Typ I ist pseudorhombisch; eine der a-Achsen verleiht ihm stark polare Gestalt. Als größte Fläche ist das re. trig. Prisma II. St.
, entwickelt. Das Trapezoeder
erscheint an zwei Stellen vizinal. Typ II ist nach einer der Winkelhalbierenden der a-Achsen gestreckt. In dieser Richtung betrachtet erscheint der Kristall tetragonal, da auf diese Weise die unter rechtem Winkel stehenden Flächen
, (0001),
und
das Quadrat begrenzen. Dies sind zugleich die größtentwickelten Flächen. Typ III ist isometrisch; sämtliche Flächen (Prismen, beide Rhomboeder sowie das Basisendflächenpaar) sind etwa gleich stark entwickelt. In Richtung auf das pos. Rhomboeder betrachtet, erweckt dieser Typ den Eindruck eines kubischen Kristalles. Hier fehlen trig. Prisma und das Trapezoeder.
Summary Quarz crystals, grown by Dr.Baumann, Heidelberg, are remarkable not only for their extraordinary transparency but also for a conspicuous morphology. Three completely different types are described. Type I is pseudo-orthorhombic; one of the a-axes causes a strongly polar appearance. Largest face is the right trig. prism II. position . The trapezohedron appears in two positions as vicinals. Type II is alongated parallel to one of the bisectrices of the a-axes. Viewed in this direction the crystal seems to be tetragonal, as the faces , (0001), and , which are at right angles to each other, form a square; these faces are at the same time the largest ones. Typ III is isometric; all the faces (prisms, both rhombohedrons, and the pinacoid) are of approximately the same size. Viewed in the direction upon the pos. rhombohedron this type appears to be cubic. The trig. prism and the trapezohedron are here missing. Mit 4 Figuren und 3 Textabbildungen Herrn Professor Dr.F. Machatschki zum 70. Geburtstag gewidmet. 相似文献 12.
Zur Bestimmung einer definierten mittleren Lichtbrechung optisch einachsiger Minerale im Dünnschliff
Prof. Dr. Rudolf Mosebach 《Contributions to Mineralogy and Petrology》1954,4(3):269-287
Zusammenfassung Durch Gangunterschiedsbestimmungen in der auf dem Drehtisch eingemessenen Kreisschnittebene optisch einachsiger Kristalle läßt rich eine mittlere Lichtbrechung
theoretisch ableiten and experimentell direkt bestimmen. Ein graphisches and ein rechnerisches Verfahren zur Gewinnung der
aus den Ganguntersehieden wird entwickelt and an Quarz, Korund, Zirkon, Turmalin und Eisenorthoklas ausprobiert. Man erhält für die mittlere Lichtbrechung Werte, die günstigenfalls mit der Immersionsmethode an Genauigkeit vergleichbar sind. 相似文献
13.
Pr. Heinz Meixner 《Mineralogy and Petrology》1954,4(1-4):277-282
Zusammenfassung Die nach einer Scheinbasis tafeligen Magnesitkristalle von Asturreta (und ebenso ähnliche Dolomitkristalle aus den Magnesitlagerstätten Sunk, Oberdorf und Lanersbach) liefern bei Einbettung in den meisten üblichen Immersionsmitteln bei konoskopischer Beobachtung nicht ein, sondern drei einachsige Achsenbilder. Die Erscheinung wird nicht etwa durch Verzwillingung verursacht, sondern, da die Scheinbasis aus zahlreichen winzigen, streng parallelen r
aufgebaut ist, durch einen Summeneffekt der symmetriebedingten
-Flächenlagen in Abhängigkeit vom Einbettungsmittel. Das konnte durch Rechnung und Messung bewiesen werden.Mit 4 Textabbildungen. 相似文献
14.
Jeffrey A. Grambling 《Contributions to Mineralogy and Petrology》1986,94(2):149-164
Two metamorphic isograds cut across graphitic schist near Pecos Baldy, New Mexico. The southern isograd marks the first coexistence of staurolite with biotite, whereas the northern isograd marks the first coexistence of andalusite with biotite. The isograds do not record changes in temperature or pressure. Instead, they record a regional gradient in the composition of the metamorphic fluid phase. Ortega Quartzite, which contains primary hematite, lies immediately north of the graphitic schist. Mineral compositions within the schist change gradually toward the quartzite, reflecting gradients in
and
. The chemical potential gradients, locally as high as 72 cal/m in
and 9 cal/m in
, controlled the positions of the two mapped isograds. The staurolite-biotite isograd records where
fell below 0.80, at
near 10–23 bars; the andalusite-biotite isograd records where
fell below 0.25, at
near 10–22 bars. Dehydration and oxidation were coupled by graphite-fluid equilibrium.The chemical potential gradients apparently formed during metamorphism, as graphite in schist reacted with hematite in quartzite. Local oxidation of graphite formed CO2 which triggered dehydration reactions along the schistquartzite contact. This process created a C-O-H fluid which infiltrated into overlying rocks. Upward infiltration, local fluid-rock equilibration and additional infiltration proceeded until the composition of the infiltrating fluid evolved to that in equilibrium with the infiltrated rock. This point occurs very close to the staurolite-biotite isograd. Pelitic rocks structurally above this isograd show no petrographic evidence of infiltration, even though calculations indicate that volumetric fluid/rock ratios may have exceeded 15 and thin, rare calc-silicate beds show extensive K-metasomatism and quartz veining. 相似文献
15.
J. W. Jones 《Contributions to Mineralogy and Petrology》1972,37(4):291-306
In the Rogers Pass area of British Columbia the almandine garnet isograd results from a reaction of the form: 5.31 ferroan-dolomite+8.75 paragonite+4.80 pyrrhotite+3.57 albite+16.83 quartz+1.97 O2=1.00 garnet+16.44 andesine+1.53 chlorite+2.40 S2+1.90 H2O+10.62 CO2. The coefficients of this reaction are quite sensitive to the Mn content of ferroan-dolomite.Experimental data applied to mineral compositions present at the isograd, permits calculation of two intersecting P, T equilibrium curves. P=29088–39.583 T is obtained for the sub-system paragonite-margarite (solid-solution), plagioclase, quartz, ferroan-dolomite, and P=28.247 T–14126 is obtained for the sub-system epidote, quartz, garnet, plagioclase. These equations yield P=3898 bars and T=638° K (365° C). These values are consistent with the FeS content of sphalerite in the assemblage pyrite, pyrrhotite, sphalerite and with other estimates for the area.At these values of P and T the composition of the fluid phase in equilibrium with graphite in the system C-O-H-S during the formation of garnet is estimated as:
bars,
bars,
bars,
bars,
bars,
bars,
bars,
bars,
, bars,
bars. 相似文献
16.
D. S. Coombs Y. Kawachi B. F. Houghton G. Hyden I. J. Pringle J. G. Williams 《Contributions to Mineralogy and Petrology》1977,63(3):229-246
Almost pure andradite and intermediate members of the andradite-grossular series (gros40–49, and 47–54, py0–3, alm0–3, spess0–2, hydrogarnet0–3), often framboidal in habit, are widespread in metabasites including lavas, minor intrusions, and volcanic sandstones and
breccias metamorphosed under prehnite-pumpellyite and pumpellyite-actinolite facies conditions, possibly extending into the
zeolite facies. Coexisting phases include iron-rich epidotes (100 Fe*/Fe*+Al=22–34), pumpellyite, prehnite, actinolite, and
chlorite, electron microprobe analyses of which are given, as well as quartz, albite, and calcite. Zoisite (100 Fe*/Fe*+Al=1–5)
and iron-poor epidote (100 Fe*/Fe*+Al=11–18) occur in 2 rocks in pseudomorphs after plagioclase together with more iron-rich
epidote, but not in close association with the garnets. Coexisting pumpellyite is iron-rich (FeO* 9–14%) in the prehnite-pumpellyite
facies and iron-poor (FeO* 5%) in the pumpellyiteactinolite facies. Chlorites and actinolites vary widely and sympathetically
in FeO/MgO+FeO ratio. Andradite is also described from a stilpnomelane-actinolite-hematite-bearing andradite quartzite of
the pumpellyite-actinolite facies.
Conditions of formation involved temperatures of 300 to 400 ° or less, at pressures up to a few kilobars. A wide range of
oxygen fugacities is possible, but
in the fluid phase was low. Grandite and chlorite are incompatible in the pumpellyite-actinolite and greenschist facies in
the presence of quartz but the 2 minerals occur together in some pumpellyite-actinolite facies assemblages as a result of
incomplete reaction and/or local deficiency in silica. In the greenschist facies the association is replaced by epidote-actinolite±hematite
and sodic amphibole.
Whereas at medium to high grades of metamorphism andradite and grandite are characteristic of skarns irrespective of
, at very low grades they are found in mafic volcanic rocks and volcanogenic sediments as well as in certain cherty rocks
of unusual composition, rodingites, and serpentinites, where
was very low. 相似文献
17.
Trace element analyses of 1-atm and high-pressure experiments show that in komatiite and peridotite, the olivine (OL)/liquid (L) distribution coefficient for Al2O3 (
) increases with pressure and temperature. Olivine in equilibrium with liquid accepts as much as 0.2 wt% Al2O3 in solution at 6 GPa. Convergence to equilibrium compositions at this high level is shown by cation diffusion of Al into synthetic forsterite crystals of low-Al contents in the presence of melt. Convergence to low-Al equilibrium compositions at lower P and T is shown by diffusion of Al out of synthetic forsterite with high initial Al content. Isobaric and isothermal experimental data subsets reveal that temperature and pressure variations both have real effects on
. Variation in silicate melt composition has no detectable effect on
within the limited range of experimentally investigated mixtures. Least-squares regression for 24 experiments, using komatiite and peridotite, performed at 1 atm to 6 GPa and 1300 to 1960°C, gives the best fit equation:
Increase in
with increasingly higher-pressure melting is consistent with incorporation of a spinel-like component of low molar volume into olivine, although other substitutions possibly involving more complex coupling cannot be ruled out. High P-T ultrabasic melting residues, if pristine, may be recognized by the high
calculated from microprobe analyses of Al2O3 concentrations in residual olivines and estimated Al2O3 concentration in the last liquid removed. In general the low levels of Al in natural olivine from mantle xenoliths suggest that pristine residues are rarely recovered. 相似文献
18.
Prof. Dr. K. Walenta 《Mineralogy and Petrology》1977,24(3):125-132
Zusammenfassung Machatschkiit ist ein neues wasserhaltiges Calciumarsenat, das in der Grube Anton bei Schiltach im mittleren Schwarzwald (BRD) 1960 gefunden wurde. Es kommt zusammen mit Gips, Pharmakolith, Pikropharmakolith und Sainfeldit als Sekundärbildung krustenförmig auf Granit vor.Als charakteristische Form tritt das Rhomboeder
auf. Keine Spaltbarkeit, Bruch muschelig, Härte 2–3,G=2,5 bis 2,6 g·cm–3,D
x
=2,50 g·cm–3, farblos, durchsichtig bis durchscheinend. Optische Daten:n
=1,585±0,002,n
=1,593±0,002, einachsig oder schwach zweiachsig, negativ.Gitterkonstanten:a
0=15,10,c
0=22,59 Å,a
0c
0=11,4960,Z=12;a
rh
=11,52 Å, =81°52,Z=4. Mögliche Raumgruppen:R32,R3m,
. Stärkste Linien des Pulverdiagramms: 8,59 (10)
(110), 5,34 (8)
(210), 3,59 (8)
. Eine chemische Analyse ergab nach Umrechnung folgende Zusammensetzung: CaO 29,5%, As2O5 40,8%, SO3 0,5%, H2O 29,2%, Summe 100,0%. Dies kommt der Formel Ca3(AsO4)2 · 9 H2O sehr nahe. In verdünnter HCl und HNO3 ist der Machatschkiit leicht löslich.
Machatschkiite, a new arsenate mineral from the Anton Mine in the Heubach valley near Schiltach (Black Forest, Federal Republic of Germany) Summary Machatschkiite is a new hydrous calcium arsenate which was found 1960 in the Anton Mine near Schiltach in the central Black Forest. It is a secondary mineral which occurs in crusts on granite in association with gypsum, pharmacolite, picropharmacolite and sainfeldite.The characteristic form is the rhombohedron . No cleavage, fracture conchoidal, hardness 2–3,G=2.5–2.6 g·cm–3,D x =2.50 g·cm–3, colourless, transparent to translucent. Optical data:n =1.585±0.002,n =1.593±0.002, uniaxial or weakly biaxial, negative.Unit-cell dimensions:a 0=15.10,c 0=22.59 Å,a 0c 0=11.4960,Z=12;a rh =11.52 Å, =81°52,Z=4. Possible space groups:R32,R3m, . Strongest lines of the powder pattern: 8.59 (10) (110), 5.34 (8) (210), 3.59 (8) . A chemical analysis gave the following composition after recalculation: CaO 29.5%, As2O5 40.8%, SO3 0.5%, H2O 29.2%, total 100.0%. This agrees well with the formula Ca3(AsO4)2 · 9 H2O. Machatschkiite is easily soluble in diluted HCl and HNO3. Mit 3 Abbildungen 相似文献 19.
Near-liquidus phase relationships of a spinel lherzolite-bearing olivine melilitite from Tasmania were investigated over a P, T range with varying
,
, and
. At 30 kb under MH-buffered conditions, systematic changes of liquidus phases occur with increasing
(
= CO2/CO2 +H2O+olivine melilitite). Olivine is the liquidus phase in the presence of H2O alone and is joined by clinopyroxene at low
. Increasing
eliminates olivine and clinopyroxene becomes the only liquidus phase. Further addition of CO2 brings garnet+orthopyroxene onto the liquidus together with clinopyroxene, which disappears with even higher CO2. The same systematic changes appear to hold at higher and lower pressures also, only that the phase boundaries are shifted to different
. The field with olivine- +clinopyroxene becomes stable to higher
with lower pressure and approaches most closely the field with garnet+orthopyroxene+clinopyroxene at about 27 kb, 1160 °C,
0.08 and
0.2 (i.e., 6–7% CO2+ 7–8% H2O). Olivine does not coexist with garnet+orthopyroxene+clinopyroxene under these MH-buffered conditions. Lower oxygen fugacities do not increase the stability of olivine to higher
and do not change the phase relationships and liquidus temperatures drastically. Thus, it is inferred that olivine melilitite 2927 originates as a 5% melt (inferred from K2
O and P2O5 content) from a pyrolite source at about 27kb, 1160 dg with about 6–7% CO2 and 7–8% H2O dissolved in the melt. The highly undersaturated character of the melt and the inability to find olivine together with garnet and orthopyroxene on the liquidus (in spite of the close approach of the respective liquidus fields) can be explained by reaction relationships of olivine and clinopyroxene with orthopyroxene, garnet and melt in the presence of CO2. 相似文献
20.
On the basis of ore-forming periods and stages of the Dachang ore field, the pH and
conditions and the S isotopic systematics during ore formation have been thcrmodynamically treated in this paper. Calculations
show a progressively decreased pH, an increased oxidation regime and an intensified activity of sulfur from the early to the
late stage. Owing to the unreliability of inferring the S source from δ34Smin,
has been calculated using the Ohmoto’s model. Results indicate that the δ34
min frequency distribution is more concentrated than that of δ34Smin and the peak value shifts to negative region by 2.5%. The sulfur in the whole ore field seems to be of multiple source, i.e.,
different deposits have their own S sources. But the S isotopic composition pertaining to each stage is nearly constant, suggesting
that the ore-forming system be open to sulfur and the supply of sulfur be sufficient. The conclusions deduced from calculations
are supported by many lines of geological evidence. 相似文献
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