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1.
Francisco J. Alcalá Yolanda Cantón Sergio Contreras Ana Were Penélope Serrano-Ortiz Juan Puigdefábregas Albert Solé-Benet Emilio Custodio Francisco Domingo 《Environmental Earth Sciences》2011,62(3):541-557
In the high-permeability, semiarid carbonate aquifer in the Sierra de Gádor Mountains (southeastern Spain), some local springs
draining shallow perched aquifers were of assistance in assessing applicability of the atmospheric chloride mass balance (CMB)
for quantifying total yearly recharge (R
T) by rainfall. Two contrasting hydrological years (October through September) were selected to evaluate the influence of climate
on recharge: the average rainfall year 2003–2004, and the unusually dry 2004–2005. Results at small catchment scale were calibrated
with estimated daily stand-scale R
T obtained by means of a soil water balance (SWB) of rainfall, using the actual evapotranspiration measured by the eddy covariance
(EC) technique. R
T ranged from 0.35 to 0.40 of rainfall in the year, with less than a 5% difference between the CMB and SWB methods in 2003–2004.
R
T varied from less than 0.05 of rainfall at mid-elevation to 0.20 at high elevation in 2004–2005, with a similar difference
between the methods. Diffuse recharge (R
D) by rainfall was quantified from daily soil water content field data to split R
T into R
D and the expected concentrated recharge (R
C) at catchment scale in both hydrological years. R
D was 0.16 of rainfall in 2003–2004 and 0.01 in 2004–2005. Under common 1- to 3-day rainfall events, the hydraulic effect of
R
D is delayed from 1 day to 1 week, while R
C is not delayed. This study shows that the CMB method is a suitable tool for yearly values complementing and extending the
more widely used SWB in ungauged mountain carbonate aquifers with negligible runoff. The slight difference between R
T rates at small catchment and stand scales enables results to be validated and provides new estimates to parameterize R
T with rainfall depth after checking the weight of diffuse and concentrated mechanisms on R
T during moderate rainfall periods and episodes of marked climatic aridity. 相似文献
2.
Konstantin D. Litasov Anton Shatskiy Eiji Ohtani Tomoo Katsura 《Physics and Chemistry of Minerals》2011,38(1):75-84
The H2O content of wadsleyite were measured in a wide pressure (13–20 GPa) and temperature range (1,200–1,900°C) using FTIR method.
We confirmed significant decrease of the H2O content of wadsleyite with increasing temperature and reported first systematic data for temperature interval of 1,400–1,900°C.
Wadsleyite contains 0.37–0.55 wt% H2O at 1,600°C, which may be close to its water storage capacity along average mantle geotherm in the transition zone. Accordingly,
water storage capacity of the average mantle in the transition zone may be estimated as 0.2–0.3 wt% H2O. The H2O contents of wadsleyite at 1,800–1,900°C are 0.22–0.39 wt%, indicating that it can store significant amount of water even
under the hot mantle environments. Temperature dependence of the H2O content of wadsleyite can be described by exponential equation
C\textH2 \textO = 6 3 7.0 7 \texte - 0.00 4 8T , C_{{{\text{H}}_{2} {\text{O}}}} = 6 3 7.0 7 {\text{e}}^{ - 0.00 4 8T} , where T is in °C. This equation is valid for temperature range 1,200–2,100°C with the coefficient of determination R
2 = 0.954. Temperature dependence of H2O partition coefficient between wadsleyite and forsterite (D
wd/fo) is complex. According to our data apparent Dwd/fo decreases with increasing temperature from D
wd/fo = 4–5 at 1,200°C, reaches a minimum of D
wd/fo = 2.0 at 1,400–1,500°C, and then again increases to D
wd/fo = 4–6 at 1,700–1,900°C. 相似文献
3.
Northeast India region is one of the most seismically active areas in the world. Events data for the period 1897–2010, used
in this study has been largely compiled from global ISC, NEIC and GCMT databases. Historical seismicity catalogue of Gupta
et al (1986) and some events data from the bulletins of India Meteorological Department are also used. Orthogonal regression relations
for conversion of body and surface wave magnitudes to M
w,HRVD based on events data for the period 1978–2006 have been derived. An Orthogonal Standard Regression (OSR) relationship has
also been obtained for scaling of intensity estimates to M
w,NEIC using 126 global intensity events with intensity VI or greater during the period 1975–2010. 相似文献
4.
On the Ratios between Elastic Modulus and Uniaxial Compressive Strength of Heterogeneous Carbonate Rocks 总被引:3,自引:3,他引:0
V. Palchik 《Rock Mechanics and Rock Engineering》2011,44(1):121-128
The ratios M
R = E/σ
c for 11 heterogeneous carbonate (dolomites, limestones and chalks) rock formations collected from different regions of Israel
were examined. Sixty-eight uniaxial compressive tests were conducted on weak-to-strong (5 MPa < σ
c < 100 MPa) and very strong (σ
c > 100 MPa) rock samples exhibiting wide ranges of elastic modulus (E = 6100–82300 MPa), uniaxial compressive strength (σ
c = 14–273.9 MPa), Poisson's ratio (ν = 0.13–0.49), and dry bulk density (ρ = 1.7–2.7 g/cm3). The observed range of M
R = 60.9–1011.4 and mean value of M
R = 380.5 are compared with the results obtained by Deere (Rock mechanics in engineering practice, Wiley, London, pp 1–20,
1968) for limestones and dolomites, and the statistical analysis of M
R distribution is performed. Mutual relations between E, σ
c, ρ, M
R for all studied rocks, and separately for concrete rock formations are revealed. Linear multiple correlations between E on the one hand and σ
c and ρ on the other for Nekorot and Bina limestone and Aminadav dolomite are obtained. It is established that the elastic modulus
and M
R in very strong carbonate samples are more correlated with ρ−σ
c combination and ε
a max, respectively, than in weak to strong samples. The relation between M
R and maximum axial strain (ε
a max) for all studied rock samples (weak-to-strong and very strong) is discussed. 相似文献
5.
The equilibrium water content of cordierite has been measured for 31 samples synthesized at pressures of 1000 and 2000 bars
and temperatures from 600 to 750° C using the cold-seal hydrothermal technique. Ten data points are presented for pure magnesian
cordierite, 11 data points for intermediate iron/magnesium ratios from 0.25 to 0.65 and 10 data points for pure iron cordierite.
By representing the contribution of H2O to the heat capacity of cordierite as steam at the same temperature and pressure, it is possible to calculate a standard
enthalpy and entropy of reaction at 298.18° K and 1 bar for,
(Mg,Fe)2Al4Si5O18+H2O ⇄ (Fe,Mg)2Al4Si5O18.H2O
Combining the 31 new data points with 89 previously published experimental measurements gives: ΔH
°
r
=–37141±3520 J and ΔS
°
r
=–99.2±4 J/degree. This enthalpy of reaction is within experimental uncertainty of calorimetric data. The enthalpy and entropy
of hydration derived separately for magnesian cordierite (–34400±3016 J, –96.5±3.4 J/degree) and iron cordierite (–39613±2475,
–99.5±2.5 J/degree) cannot be distinguished within the present experimental uncertainty. The water content as a function of
temperature, T(K), and water fugacity, f(bars), is given by n
H2O=1/[1+1/(K ⋅ f
H2O)] where the equilibrium constant for the hydration reaction as written above is, ln K=4466.4/T–11.906 with the standard state for H2O as the gas at 1 bar and T, and for cordierite components, the hydrous and anhydrous endmembers at P and T.
Received: 2 August 1994/Accepted: 7 February 1996 相似文献
6.
M. Akaogi H. Kojitani H. Yusa R. Yamamoto M. Kido K. Koyama 《Physics and Chemistry of Minerals》2005,32(8-9):603-613
Phase transitions in MgGeO3 and ZnGeO3 were examined up to 26 GPa and 2,073 K to determine ilmenite–perovskite transition boundaries. In both systems, the perovskite
phases were converted to lithium niobate structure on release of pressure. The ilmenite–perovskite boundaries have negative
slopes and are expressed as P(GPa)=38.4–0.0082T(K) and P(GPa)=27.4−0.0032T(K), respectively, for MgGeO3 and ZnGeO3. Enthalpies of SrGeO3 polymorphs were measured by high-temperature calorimetry. The enthalpies of SrGeO3 pseudowollasonite–walstromite and walstromite–perovskite transitions at 298 K were determined to be 6.0±8.6 and 48.9±5.8 kJ/mol,
respectively. The calculated transition boundaries of SrGeO3, using the measured enthalpy data, were consistent with the boundaries determined by previous high-pressure experiments.
Enthalpy of formation (ΔH
f°) of SrGeO3 perovskite from the constituent oxides at 298 K was determined to be −73.6±5.6 kJ/mol by calorimetric measurements. Thermodynamic
analysis of the ilmenite–perovskite transition boundaries in MgGeO3 and ZnGeO3 and the boundary of formation of SrSiO3 perovskite provided transition enthalpies that were used to estimate enthalpies of formation of the perovskites. The ΔH
f° of MgGeO3, ZnGeO3 and SrSiO3 perovskites from constituent oxides were 10.2±4.5, 33.8±7.2 and −3.0±2.2 kJ/mol, respectively. The present data on enthalpies
of formation of the above high-pressure perovskites were combined with published data for A2+B4+O3 perovskites stable at both atmospheric and high pressures to explore the relationship between ΔH
f° and ionic radii of eightfold coordinated A2+ (R
A) and sixfold coordinated B4+ (R
B) cations. The results show that enthalpy of formation of A2+B4+O3 perovskite increases with decreasing R
A and R
B. The relationship between the enthalpy of formation and tolerance factor (
R
o: O2− radius) is not straightforward; however, a linear relationship was found between the enthalpy of formation and the sum of
squares of deviations of A2+ and B4+ radii from ideal sizes in the perovskite structure. A diagram showing enthalpy of formation of perovskite as a function of
A2+ and B4+ radii indicates a systematic change with equienthalpy curves. These relationships of ΔH
f° with R
A and R
B can be used to estimate enthalpies of formation of perovskites, which have not yet been synthesized. 相似文献
7.
Relative humidity (
P\textH 2 \textO P_{{{\text{H}}_{ 2} {\text{O}}}} , partial pressure of water)-dependent dehydration and accompanying phase transitions in NAT-topology zeolites (natrolite,
scolecite, and mesolite) were studied under controlled temperature and known
P\textH 2 \textO P_{{{\text{H}}_{ 2} {\text{O}}}} conditions by in situ diffuse-reflectance infrared Fourier transform spectroscopy and parallel X-ray powder diffraction.
Dehydration was characterized by the disappearance of internal H2O vibrational modes. The loss of H2O molecules caused a sequence of structural transitions in which the host framework transformation path was coupled primarily
via the thermal motion of guest Na+/Ca2+ cations and H2O molecules. The observation of different interactions of H2O molecules and Na+/Ca2+ cations with host aluminosilicate frameworks under high- and low-
P\textH 2 \textO P_{{{\text{H}}_{ 2} {\text{O}}}} conditions indicated the development of different local strain fields, arising from cation–H2O interactions in NAT-type channels. These strain fields influence the Si–O/Al–O bond strength and tilting angles within and
between tetrahedra as the dehydration temperature is approached. The newly observed infrared bands (at 2,139 cm−1 in natrolite, 2,276 cm−1 in scolecite, and 2,176 and 2,259 cm−1 in mesolite) result from strong cation–H2O–Al–Si framework interactions in NAT-type channels, and these bands can be used to evaluate the energetic evolution of Na+/Ca2+ cations before and after phase transitions, especially for scolecite and mesolite. The 2,176 and 2,259 cm−1 absorption bands in mesolite also appear to be related to Na+/Ca2+ order–disorder that occur when mesolite loses its Ow4 H2O molecules. 相似文献
8.
Summary Batiferrite, ideally Ba[Ti2Fe10]O19, was found in the Quaternary volcanic rocks near üdersdorf, Graulai, and Altburg, western Eifel area, Germany. The new mineral
typically occurs as euhedral platy grains in cavities of melilite- and leucite-nephelinite basalts. Associated minerals are
hematite, magnetite, titanite, g?tzenite, clinopyroxene, nepheline, and biotite. It exhibits a hexagonal tabular habit flattened
on {0001}, diameter 0.5–1 mm, thickness 20–125 μm, and {10&1macr;3}, {10&1macr;0} as observable forms. The mineral is opaque, of black
color with submetallic lustre, and shows a ferrimagnetic behavior. VHN50 is 793 with a range of 710–841 from ten indentations. The quantitative reflectance measurements of Ro/Re on oriented grains in air and oil immersion, respectively, are [%]: for 470 nm 22.1/20.1 and 8.4/7.1, for 546 nm 21.0/19.4
and 7.8/6.6, for 589 nm 20.2/18.8 and 7.4/6.3, and for 650 nm 19.3/18.3 and 6.8/5.9. The bireflectance is distinct (air) to
weak (oil), and parallel (0001) a moderate anisotropy with straight extinction can be observed. Typical microprobe analyses
give [wt%] K2O 0.28–0.33, Na2O 0.17–0.20, SrO 0.46–0.55, BaO 11.80–12.17, MgO 1.27–1.47, Al2O3 0.31–0.33, TiO2 13.11–13.63, MnO 2.38–2.57, Fe2O3 61.36–63.12, FeO 5.49–5.86 (Fe3+/Fe2+ calculated for charge compensation), which is equivalent to (Ba0.84Na0.06K0.06Sr0.05)1.01(Fe8.48
3+Fe0.86
2+Ti1.82Mg0.37Mn0.37Al0.06)11.96O19 as the average composition based on 19 oxygen atoms. Batiferrite is a magnetoplumbite-type mineral with hexagonal symmetry,
space group P6
3
/mmc (no. 194), a = 5.909(1) ?, c = 23.369(4) ?, V = 706.6(2) ?3, Z = 2, and a calculated density of 5.016 gcm−3. The structure was refined to R1 = 0.031 for 278 unique reflections with Fo
2 > 4σ (Fo
2) and R1 = 0.079 for all 452 unique observations using single crystal X-ray data. The strongest reflections of the X-ray powder diffraction
pattern are [d
obs, I/Io, (hkl)]: 2.631, 100, (114); 2.799, 80, (107); 1.478, 70, (220); 2.429, 60, (203); 1.672, 50, (217). The new mineral is comparable to the other Ba containing magnetoplumbite-type minerals haggertyite and
hawthorneite, the iron content, however, is much higher and in the range of magnetoplumbite. The large cation site (A) is
dominated by Ba, and four of the five remaining crystallographic cation sites in the structure are dominated by Fe (M1, 2,
3, 5), the octahedrally coordinated M4-site is dominated by Ti. No oxygen vacancy on the O3-site like in plumboferrite can
be observed. Batiferrite is named for its main chemical composition and the relationship to the M-type hexaferrites (polytype
5H).
Received December 14, 1999; accepted March 2, 2000 相似文献
Zusammenfassung Batiferrit, ein neues ferrimagnetisches Mineral des Magnetoplumbit-Typs aus den quart?ren Vulkaniten der West-Eifel, Deutschland Das neue Mineral Batiferrite, mit der Idealformel Ba[Ti2Fe10]O19, wurde an drei Fundpunkten in den Quart?ren Vulkangesteinen der westlichen Eifel, Deutschland, in der N?he von üdersdorf, Graulai und Altburg gefunden. Das neue Mineral tritt typischerweise bl?ttchenf?rmig in kleinen Hohlr?umen von Melilith- und Leucit-Nephelininit Basalten auf. Vergesellschaftete Minerale sind H?matit, Magnetit, Titanit, G?tzenit, Klinopyroxen, Nephelin und Biotit. Der Habitus ist hexagonal tafelig nach {0001}, mit einem Durchmesser von 0.5–1 mm und einer Dicke von 20–125 μm, zus?tzlich k?nnen die Formen {10&1macr;3} und {10&1macr;0} beobachtet werden. Das Mineral ist opak, hat eine schwarze Farbe mit einem leicht metallischen Glanz, und ist ferromagnetisch. Die H?rte VHN50 ist 793 mit einem Bereich von 710–841 aus 10 Eindruckbestimmungen. Die quantitativen Reflexionsmessungen von Ro/Re an orientierten K?rnern in Luft beziehungsweise ?limmersion, ergaben [%]: für 470 nm 22.1/20.1 und 8.4/7.1, für 546 nm 21.0/19.4 und 7.8/6.6, für 589 nm 20.2/18.8 und 7.4/6.3, und für 650 nm 19.3/18.3 und 6.8/5.9. Die Bireflexion ist deutlich (Luft) bis schwach (?l) und parallel (0001) kann eine mittlere Anisotropie mit gerader Ausl?schung beobachtet werden. Eine typische Mikrosondenanalyse ergibt [wt%] K2O 0.28–0.33, Na2O 0.17–0.20, SrO 0.46–0.55, BaO 11.80–12.17, MgO 1.27–1.47, Al2O3 0.31–0.33, TiO2 13.11–13.63, MnO 2.38–2.57, Fe2O3 61.36–63.12, FeO 5.49–5.86 (Fe3+/Fe2+ berechnet zum Ladungsausgleich), die mittlere chemische Formel auf der Basis von 19 Sauerstoffatomen lautet (Ba0.84Na0.06K0.06Sr0.05)1.01 (Fe8.48 3+Fe0.86 2+Ti1.82Mg0.37Mn0.37Al0.06)11.96O 19. Batiferrit ist ein Mineral der Magnetoplumbitgruppe, hat hexagonale Symmetrie mit der Raumgruppe P63/mmc (Nr. 194), a = 5.909(1) ?, c = 23.369(4) ?, V = 706.6(2) ?3, Z = 2, und einer berechneten Dichte von 5.016 gcm−3. Die Struktur wurde aus Einkristall-R?ntgendaten bis zu einem R1-Wert von 0.031 für 278 Fo 2 > 4σ(Fo 2), und einem R1-Wert von 0.079 für alle 452 Fo 2 verfeinert. Die st?rksten Beugungsreflexe der Pulver-R?ntgendaten sind [dobs, I/Io, (hkl)]: 2.631, 100, (114); 2.799, 80, (107); 1.478, 70, (220); 2.429, 60, (203); 1.672, 50, (217). Das neue Mineral weist deutliche ?hnlichkeiten zu den anderen beiden Ba-reichen Mineralen Haggertyit und Hawthorneit der Magnetoplumbit-Gruppe auf, jedoch ist der Eisengehalt wesentlich h?her und im Bereich des Minerals Magnetoplumbit. Der gro?e Kationenplatz (A) ist von Barium dominiert, vier (M1, 2, 3, 5) der restlichen fünf kristallographischen Kationenpl?tze in der Struktur sind fast ausschlie?lich mit Fe, die oktaedrisch koordinierte M4-Position ist überwiegend mit Ti besetzt. An der O3-Position konnte kein Sauerstoffdefizit wie in Plumboferrit festgestellt werden. Batiferrit ist nach seiner chemischen Beschaffenheit und nach seiner Zugeh?hrigkeit zu den M-Typ Hexaferriten (Polytyp 5H) benannt.
Received December 14, 1999; accepted March 2, 2000 相似文献
9.
The melting reaction: albite(solid)+ H2O(fluid) =albite-H2O(melt) has been determined in the presence of H2O–NaCl fluids at 5 and 9.2 kbar, and results compared with those obtained in presence of H2O–CO2 fluids. To a good approximation, albite melts congruently at 9 kbar, indicating that the melting temperature at constant
pressure is principally determined by water activity. At 5 kbar, the temperature (T)- mole fraction (X
(H2O) ) melting relations in the two systems are almost coincident. By contrast, H2O–NaCl mixing at 9 kbar is quite non-ideal; albite melts ∼70 °C higher in H2O–NaCl brines than in H2O–CO2 fluids for X
(H2O) =0.8 and ∼100 °C higher for X
(H2O) =0.5. The melting temperature of albite in H2O–NaCl fluids of X
(H2O)=0.8 is ∼100 °C higher than in pure water. The P–T curves for albite melting at constant H2O–NaCl show a temperature minimum at about 5 kbar. Water activities in H2O–NaCl fluids calculated from these results, from new experimental data on the dehydration of brucite in presence of H2O–NaCl fluid at 9 kbar, and from previously published experimental data, indicate a large decrease with increasing fluid pressure
at pressures up to 10 kbar. Aqueous brines with dissolved chloride salt contents comparable to those of real crustal fluids
provide a mechanism for reducing water activities, buffering and limiting crustal melting, and generating anhydrous mineral
assemblages during deep crustal metamorphism in the granulite facies and in subduction-related metamorphism. Low water activity
in high pressure-temperature metamorphic mineral assemblages is not necessarily a criterion of fluid absence or melting, but
may be due to the presence of low a
(H2O) brines.
Received: 17 March 1995/Accepted: 9 April 1996 相似文献
10.
H2O activity in concentrated NaCl solutions at high pressures and temperatures measured by the brucite-periclase equilibrium 总被引:1,自引:0,他引:1
H2O activities in concentrated NaCl solutions were measured in the ranges 600°–900° C and 2–15 kbar and at NaCl concentrations
up to halite saturation by depression of the brucite (Mg(OH)2) – periclase (MgO) dehydration equilibrium. Experiments were made in internally heated Ar pressure apparatus at 2 and 4.2
kbar and in 1.91-cm-diameter piston-cylinder apparatus with NaCl pressure medium at 4.2, 7, 10 and 15 kbar. Fluid compositions
in equilibrium with brucite and periclase were reversed to closures of less than 2 mol% by measuring weight changes after
drying of punctured Pt capsules. Brucite-periclase equilibrium in the binary system was redetermined using coarsely crystalline
synthetic brucite and periclase to inhibit back-reaction in quenching. These data lead to a linear expression for the standard
Gibbs free energy of the brucite dehydration reaction in the experimental temperature range: ΔG° (±120J)=73418–134.95T(K). Using this function as a baseline, the experimental dehydration points in the system MgO−H2O−NaCl lead to a simple systematic relationship of high-temperature H2O activity in NaCl solution. At low pressure and low fluid densities near 2 kbar the H2O activity is closely approximated by its mole fraction. At pressures of 10 kbar and greater, with fluid densities approaching
those of condensed H2O, the H2O activity becomes nearly equal to the square of its mole fraction. Isobaric halite saturation points terminating the univariant
brucite-periclase curves were determined at each experimental pressure. The five temperature-composition points in the system
NaCl−H2O are in close agreement with the halite saturation curves (liquidus curves) given by existing data from differential thermal
analysis to 6 kbar. Solubility of MgO in the vapor phase near halite saturation is much less than one mole percent and could
not have influenced our determinations. Activity concentration relations in the experimental P-T range may be retrieved for the binary system H2O-NaCl from our brucite-periclase data and from halite liquidus data with minor extrapolation. At two kbar, solutions closely
approach an ideal gas mixture, whereas at 10 kbar and above the solutions closely approximate an ideal fused salt mixture,
where the activities of H2O and NaCl correspond to an ideal activity formulation. This profound pressure-induced change of state may be characterized
by the activity (a) – concentration (X) expression: a
H
2O=X
H
2O/(1+αX
NaCl), and a
NaCl=(1+α)(1+α)[X
NaCl/(1+αX
NaCl)](1+α). The parameter α is determined by regression of the brucite-periclase H2O activity data: α=exp[A–B/ϱH
2O ]-CP/T, where A=4.226, B=2.9605, C=164.984, and P is in kbar, T is in Kelvins, and ϱH
2O is the density of H2O at given P and T in g/cm3. These formulas reproduce both the H2O activity data and the NaCl activity data with a standard deviation of ±0.010. The thermodynamic behavior of concentrated NaCl solutions at
high temperature and pressure is thus much simpler than portrayed by extended Debye-Hückel theory. The low H2O activity at high pressures in concentrated supercritical NaCl solutions (or hydrosaline melts) indicates that such solutions
should be feasible as chemically active fluids capable of coexisting with solid rocks and silicate liquids (and a CO2-rich vapor) in many processes of deep crustal and upper mantle metamorphism and metasomatism.
Received: 1 September 1995 / Accepted: 24 March 1996 相似文献
11.
Summary Elevated P contents of up to 0.086 apfu (1.21 wt.% P2O5) were found in garnet from leucocratic granitic rocks (orthogneisses, granites, barren to highly evolved pegmatites) in the
Moldanubicum and Silesicum, Czech Republic, and in complex granitic pegmatites from southern California, USA, and Australia.
Minor concentrations (0.15–0.55 wt.% P2O5) appear ubiquitous in garnet from leucocratic granitic rocks of different origins and degrees of fractionation. Concentrations
of P are not related to Mn/(Mn + Fe) that vary from 0.12–0.86 and to textural types of garnet (i.e., isolated anhedral to
euhedral grains and nodules, graphic and random garnet–quartz aggregates, subsolidus veins of fine-grained garnet). Garnet
compositions exhibit negative correlations for P/Si and P/R2+ where R2+ = Fe + Mn + Mg + Ca, while Al is constant at ∼2.05 apfu. Concentrations of Na are largely below 0.02 apfu but positively correlate with P. The main substitution may involve A-site vacancy and/or the presence of some light element(s) in the crystal structure. The substitution □P2 R2+ −1Si−2 and/or alluaudite-type Na□P3 R2+ −1Si−3 seem the most likely P-incorporating mechanisms. The partitioning of P among garnet and associated minerals in granitic systems
remains unclear; however, it directly affects the distribution of Y and REEs. 相似文献
12.
I. V. Pekov N. V. Zubkova Ya. E. Filinchuk N. V. Chukanov A. E. Zadov D. Yu. Pushcharovsky E. R. Gobechiya 《Geology of Ore Deposits》2010,52(8):767-777
New minerals, shlykovite and cryptophyllite, hydrous Ca and K phyllosilicates, have been identified in hyperalkaline pegmatite
at Mount Rasvumchorr, Khibiny alkaline pluton, Kola Peninsula, Russia. They are the products of low-temperature hydrothermal
activity and are associated with aegirine, potassium feldspar, nepheline, lamprophyllite, eudialyte, lomonosovite, lovozerite,
tisinalite, shcherbakovite, shafranovskite, ershovite, and megacyclite. Shlykovite occurs as lamellae up to 0.02 × 0.02 ×
0.5 mm in size or fibers up to 0.5 mm in length usually combined in aggregates up to 3 mm in size, crusts, and parallel-columnar
veinlets. Cryptophyllite occurs as lamellae up to 0.02 × 0.1 × 0.2 mm in size intergrown with shlykovite being oriented parallel
to {001} or chaotically arranged. Separate crystals of the new minerals are transparent and colorless; the aggregates are
beige, brownish, light cream, and pale yellowish-grayish. The cleavage is parallel to (001) perfect. The Mohs hardness of
shlykovite is 2.5–3. The calculated densities of shlykovite and cryptophyllite are 2.444 and 2.185 g/cm3, respectively. Both minerals are biaxial; shlykovite: 2V
meas = −60(20)°; cryptophyllite: 2V
meas > 70°. The refractive indices are: shlykovite: α = 1.500(3), β = 1.509(2), γ = 1.515(2); cryptophyllite: α = 1.520(2), β
= 1.523(2), γ = 1.527(2). The chemical composition of shlykovite determined by an electron microprobe (H2O determined from total deficiency) is as follows, wt %: 0.68 Na2O, 11.03 K2O, 13.70 CaO, 59.86 SiO2, 14.73 H2O; the total is 100.00. The empirical formula calculated on the basis of 13 O atoms (OH/H2O calculated from the charge balance) is (K0.96Na0.09)Σ1.05Ca1.00Si4.07O9.32(OH)0.68 · 3H2O. The idealized formula is KCa[Si4O9(OH)] · 3H2O. The chemical composition of cryptophyllite determined by an electron microprobe (H2O determined from the total deficiency) is as follows, wt %: 1.12 Na2O, 17.73 K2O, 11.59 CaO, 0.08 Al2O3, 50.24 SiO2, 19.24 H2O, the total is 100.00. The empirical formula calculated on the basis of (Si,Al)4(O,OH)10 (OH/H2O calculated from the charge balance) is (K1.80Na0.17)Σ1.97Ca0.99Al0.01Si3.99O9.94(OH)0.06 · 5.07H2O. The idealized formula is K2Ca[Si4O10] · 5H2O. The crystal structures of both minerals were solved on single crystals using synchrotron radiation. Shlykovite is monoclinic;
the space group is P21/n; a = 6.4897(4), b = 6.9969(5), c = 26.714(2)?, β = 94.597(8)°, V = 1209.12(15)?3, Z = 4. Cryptophyllite is monoclinic; the space group is P21/n; a = 6.4934(14), b = 6.9919(5), c = 32.087(3)?, β = 94.680(12)°, V= 1451.9(4)?, Z = 4. The strongest lines of the X-ray powder patterns (d, ?-I, [hkl] are: shlykovite 13.33–100[002], 6.67–76[004], 6.47–55[100], 3.469–45[021], 3.068–57[$
\bar 1
$
\bar 1
21], 3.042–45[121], 2.945–62[ 23], 2.912–90[025, 12, 211]; cryptophyllite 16.01–100[002], 7.98–24[004], 6.24–48[101], 3.228–22[$
\bar 1
$
\bar 1
09], 3.197–27[0.0.10], 2.995–47[122], 2.903–84[123, 204, $
\bar 1
$
\bar 1
24, 211], 2.623–20[028, 08, 126]. Shlykovite and cryptophyllite are members of new related structural types. Their structures
are based on a two-layer packet consisting of tetrahedral Si layers linked with octahedral Ca chains. Mountainite, shlykovite
and cryptophyllite could be combined into the mountainite structural family. Shlykovite is named in memory of Russian geologist
V. G. Shlykov (1941–2007); the name cryptophyllite is from the Greek words meaning concealed and leaf that allude to its layered structure (phyllosilicate) in combination with a lamellar habit and intimate intergrowths with
visually indistinguishable shlykovite. Type specimens of the minerals are deposited at the Fersman Mineralogical Museum of
the Russian Academy of Sciences, Moscow. 相似文献
13.
J. J. Hanley J. E. Mungall T. Pettke E. T. C. Spooner C. J. Bray 《Mineralium Deposita》2005,40(3):237-256
We report methane-dominant hydrocarbon (fluid) inclusions (CH4±C2H6–C2H2, C3H8) coexisting with primary brine inclusions and secondary halide melt (solid NaCl) inclusions in Au–Pt-rich quartz-sulfide-epidote
alteration veins associated with the footwall-style Cu–PGE (platinum-group element)–Au deposits at the Fraser Mine (North
Range of the Sudbury Igneous Complex). Evidence for coentrapment of immiscible hydrocarbon–brine, and hydrocarbon–halide melt
mixtures is demonstrated. A primary CH4–brine assemblage was trapped during quartz growth at relatively low T (min. T
trapping∼145–315°C) and P (max. P
trapping∼500 bar), prior to the crystallization of sulfide minerals in the veins. Secondary inclusions contain solid halite and a
mixture of CH4, C2H6–C2H2 and C3H8 and were trapped at a minimum T of ∼710°C. The halite inclusions may represent halide melt that exsolved from crystallizing sulfide ores that texturally
postdate (by replacement) early alteration quartz hosting the primary, lower T brine–CH4 assemblage. Laser ablation ICP-MS analyses show that the brine, hydrocarbon and halide melt inclusions contain significant
concentrations of Cu (0.1–1 wt% range), Au, Bi, Ag and Pt (all 0.1–10 ppm range). Cu:Pt and Cu:Au ratios in the inclusions
are significantly (up to 4 log units) lower than in the host alteration veins and adjacent massive sulfide ore veins, suggesting
either (1) early Cu loss from the volatiles by chalcopyrite precipitation or (2) enhanced Au and Pt solubilities relative
to Cu at the temperatures of entrapment. Concentration ratios between coexisting brine and CH4 inclusions
are lower for Cu, Au, Bi and Ag than for other elements (Na, Ca, Fe, Mn, Zn, Pb) indicating that during interaction with
the brine, the hydrocarbon phase was enriched in ore metals. The high concentrations of ore metals in hydrocarbon, brine and
halide melt phases confirm that both aqueous and non-aqueous volatiles were carriers of precious metals in the Sudbury environment
over a wide range of temperatures. Volatile evolution and magmatic sulfide differentiation were clearly part of a single,
continuous process in the Sudbury footwall. The exsolution of H2O-poor volatiles from fractionated sulfide liquid may have been a principal mechanism controlling the final distribution of
PGE and Au in the footwall ore systems. The study reports the first measurements of precious metal concentrations in fluid
inclusions from a magmatic Ni–Cu–PGE environment (the Sudbury district).
Electronic Supplementary Material Supplementary material is available for this article at 相似文献
14.
Anurag Sharma 《Contributions to Mineralogy and Petrology》1996,125(2-3):263-275
The stability of pargasite in the presence of excess quartz has been determined in the range of 0.5–6.0 kbar and 500–950 °C
in the system Na2O– CaO–MgO–Al2O3–SiO2–H2O, using synthetic minerals. The experimental results from this study indicate the presence of two distinct mineral assemblage
regions: (1) a high temperature supersolidus region containing tremolitic amphibole+melt+quartz; (b) a low temperature subsolidus region consisting of Al-rich amphibole+plagioclase+enstatite+quartz. Compositional reversals have been determined for the
following three equilibria:
(a) 2 pargasite+9 quartz=tremolite+4 plagioclase (An50)+1.5 enstatite+H2O, (b) 2 pargasite+10 quartz=tremolite+4 plagioclase (An50)+talc, and (c) pargasite+diopside+5 quartz=tremolite+2 plagioclase (An50). These experiments indicate a continuous change of amphibole composition from pargasite to tremolite with increasing temperature,
and an opposite effect with increasing pressure. The third equilibria is used to constrain a site-mixing model for the pargasitic
amphiboles, which favor a single-coupled NaA-AlT1 site mixing. The thermochemical data for pargasite estimated from the reversal data of the three equilibrium reactions is
estimated as for ΔG
0
f
,Pg=−12022.11±5.2 kJ mole-1, and S
0
Pg=591.7 ±7.9 JK-1 mole-1.
Received: 31 July 1995/Accepted: 3 June 1996 相似文献
15.
Magnesian metamorphic rocks with metapelitic mineral assemblage and composition are of great interest in metamorphic petrology for their ability to constrain P–T conditions in terranes where metamorphism is not easily visible. Phase–assemblage diagrams for natural and model magnesian metapelites in the system KFMASH are presented to document how phase relationships respond to water activity, bulk composition, pressure and temperature. The phase assemblages displayed on these phase diagrams are consistent with natural mineral assemblages occurring in magnesian metapelites. It is shown that the equilibrium assemblages at high pressure conditions are very sensitive to a(H2O). Specifically, the appearance of the characteristic HP assemblage chloritoid–talc–phengite–quartz (with excess H2O) in the magnesian metapelites of the Monte Rosa nappe (Western Alps) is due to the reduction of a(H2O). Furthermore, the mineral assemblages are determined by the whole-rock FeO/(FeO+MgO) ratio and effective Al content X
A as well as P and T. The predicted mineral associations for the low- and high-X
A model bulk compositions of magnesian metapelites at high pressure are not dependent on the X
A variations as they show a similar sequence of mineral assemblages. Above 20 kbar, the prograde sequence of assemblages associated with phengite (with excess SiO2 and H2O) for low- and high-X
A bulk compositions of magnesian metapelites is: carpholite–chlorite → chlorite–chloritoid → chloritoid–talc → chloritoid–talc–kyanite → talc–garnet–kyanite → garnet–kyanite ± biotite. At low to medium P–T conditions, a low-X
A stabilises the phengite-bearing assemblages associated with chlorite, chlorite + K-feldspar and chlorite + biotite while a high-X
A results in the chlorite–phengite bearing assemblages associated with pyrophyllite, andalusite, kyanite and carpholite. A high-X
A magnesian metapelite with nearly iron-free content stabilises the talc–kyanite–phengite assemblage at moderate to high P–T conditions. Taking into account the effective bulk composition and a(H2O) involved in the metamorphic history, the phase–assemblage diagrams presented here may be applied to all magnesian metapelites that have compositions within the system KFMASH and therefore may contribute to gaining insights into the metamorphic evolution of terranes. As an example, the magnesian metapelites of the Monte Rosa nappe have been investigated, and an exhumation path with P–T conditions for the western roof of the Monte Rosa nappe has been derived for the first time. The exhumation shows first a near-isothermal decompression from the Alpine eclogite peak conditions around 24 kbar and 505°C down to approximately 8 kbar and 475°C followed by a second decompression with concomitant cooling.M. Frey: deceased 相似文献
16.
V. M. Gurevich O. L. Kuskov N. N. Smirnova K. S. Gavrichev A. V. Markin 《Geochemistry International》2009,47(12):1170-1179
The heat capacity of eskolaite Cr2O3(c) was determined by adiabatic vacuum calorimetry at 11.99–355.83 K and by differential calorimetry at 320–480 K. Experimental
data of the authors and data compiled from the literature were applied to calculate the heat capacity, entropy, and the enthalpy
change of Cr2O3 within the temperature range of 0–1800 K. These functions have the following values at 298.15 K: C
p
0 (298.15) = 121.5 ± 0.2 J K−1mol−1, S
0(298.15) = 80.95 ± 0.14 J K−1mol−1, and H
0(298.15)-H
0(0) = 15.30±0.02 kJ mol−1. Data were obtained on the transitions from the antiferromagnetic to paramagnetic states at 228–457 K; it was determined
that this transition has the following parameters: Neel temperature T
N
= 307 K, Δ
tr
S = 6.11 ± 0.12 J K−1mol−1 and δ
tr
H = 1.87 ± 0.04 kJ mol−1. 相似文献
17.
B. C. Schmidt François Holtz Bruno Scaillet Michel Pichavant 《Contributions to Mineralogy and Petrology》1997,126(4):386-400
Solidus temperatures of quartz–alkali feldspar assemblages in the haplogranite system (Qz-Ab-Or) and subsystems in the presence
of H2O-H2 fluids have been determined at 1, 2, 5 and 8 kbar vapour pressure to constrain the effects of redox conditions on phase relations
in quartzofeldspathic assemblages. The hydrogen fugacity (f
H2) in the fluid phase has been controlled using the Shaw membrane technique for moderately reducing conditions (f
H2 < 60 bars) at 1 and 2 kbar total pressure. Solid oxygen buffer assemblages in double capsule experiments have been used to
obtain more reducing conditions at 1 and 2 kbar and for all investigations at 5 and 8 kbar. The systems Qz-Or-H2O-H2 and Qz-Ab-H2O-H2 have only been investigated at moderately reducing conditions (1 and 5 kbar) and the system Qz-Ab-Or-H2O-H2 has been investigated at redox conditions down to IW (1 to 8 kbar). The results obtained for the water saturated solidi are
in good agreement with those of previous studies. At a given pressure, the solidus temperature is found to be constant (within
the experimental precision of ± 5°C) in the f
H2 range of 0–75 bars. At higher f
H2, generated by the oxygen buffers FeO-Fe3O4 (WM) and Fe-FeO (IW), the solidus temperatures increase with increasing H2 content in the vapour phase. The solidus curves obtained at 2 and 5 kbar have similar shapes to those determined for the
same quartz - alkali feldspar assemblages with H2O-CO2- or H2O-N2-bearing systems. This suggests that H2 has the behaviour of an inert diluent of the fluid phase and that H2 solubility in aluminosilicate melts is very low. The application of the results to geological relevant conditions [HM (hematite-magnetite) > f
O2 > WM] shows that increasing f
H2 produces a slight increase of the solidus temperatures (up to 30 °C) of quartz–alkali feldspar assemblages in the presence
of H2O-H2 fluids between 1 and 5 kbar total pressure.
Received: 4 March 1996 / Accepted: 22 August 1996 相似文献
18.
Sandow Mark Yidana 《Environmental Geology》2009,57(4):789-796
Surface water resources play a crucial role in the domestic water delivery system in Ghana. In addition, sustainable food
production is based on the quality and quantity of water resources available for irrigation purposes to supplement rain-fed
agricultural activities in the country. The objective of this research was to determine the main controls on the hydrochemistry
of surface water resources in the southern part of Ghana and assess the quality of water from these basins for irrigation
activities in the area. R-mode factor and cluster analyses were applied to 625 data points from 6 river basins in southern Ghana after the data had
been log transformed and standardized for homogeneity. This study finds that surface water chemistry in the south is controlled
by the chemistry of silicate mineral weathering, chemistry of rainfall, fertilizers from agricultural activities in the area,
as well as the weathering of carbonate minerals. A Gibb’s diagram plotted with total dissolved solids (TDS) on the vertical
axis against (Na+ + K+)/(Ca2+ + K+ + Na+) on the horizontal axis indicates that rock weathering plays a significant role in the hydrochemistry. Activity diagrams
for the CaO–Na2O–Al2O–SiO2–H2O and CaO–MgO–Al2O3–SiO2–H2O systems suggest that kaolinite is the most stable clay mineral phase in the system. In addition, an assessment of the irrigation
quality of water from these basins suggests that the basins are largely low sodium—low to medium salinity basins, delivering
water of acceptable quality for irrigation purposes. 相似文献
19.
Anton Beran Dominik Talla Zdenek Losos Jiri Pinkas 《Physics and Chemistry of Minerals》2010,37(3):159-166
The infrared (IR) spectra of gem-quality baryte crystals from different occurrences are characterized by relatively weak but
strongly pleochroic absorption bands at 3,280, 3,220, 3,155, and 3,115 cm−1. These bands are assigned to anti-symmetric and symmetric OH stretching vibrations of two types of H2O molecules localized on vacant Ba sites. The H–H axis of the H2O I molecule is slightly tilted from the a-axis direction, its twofold axis being nearly parallel to the b-axis, thus defining the plane of the H2O molecule practically parallel to (001). The H2O II molecule has its H–H axis parallel to the b-axis direction, with its plane lying approximately parallel to (101). The values of the total water contents of the baryte
crystals, calculated on the basis of IR spectroscopic data, are ranging from about 1.7–3.8 wt.ppm. The possible presence of
H3O+ ions is also discussed. 相似文献
20.
L. A. Koroleva N. D. Shikina P. G. Kolodina A. V. Zotov B. R. Tagirov Yu. V. Shvarov V. A. Volchenkova Yu. K. Shazzo 《Geochemistry International》2012,50(10):853-859
The hydrolysis of the Pd2+ ion in HClO4 solutions was examined at 25–70°C, and the thermodynamic constants of equilibrium K (1)0 and K (2)0were determined for the reactions Pd2+ + H2O = PdOH+ + H+ and Pd2+ + 2H2O = Pd(OH)20 + 2H+, respectively. The values of log K (1)0 = −1.66 ± 0.5 (25°C) and −0.65 ± 0.25 (50°C) and log K (2)0 = −4.34 ± 0.3 (25°C) and −3.80 ± 0.3 (50°C) were derived using the solubility technique at 0.95 confidence level. The values of log K (1)0 = −1.9 ± 0.6 (25°C), −1.0 ± 0.4 (50°C), and −0.5 ± 0.3 (70°C) were obtained by spectrophotometric techniques. The palladium ion is significantly hydrolyzed at elevated temperatures (50–70°C) even in strongly acidic solutions (pH 1–1.5), and its hydrolysis is enhanced with increasing temperature. 相似文献