We conducted a series of melting experiments in the join forsterite–diopside–leucite under 0.1 and 2.3 GPa and in the join forsterite–leucite–åkermanite under 2.3 GPa to understand paragenetic relationships amongst different types of lamproitic and lamprophyric magmas with K-rich mafic and ultramafic volcanic (kamafugitic) rocks. Both the joins were studied in the presence of excess water. The experimental results of the join forsterite–diopside–leucite at 0.1 GPa show that the five-phase point of forsterite (Fo)ss + diopside (Di)ss + leucite (Lc)ss + liquid (Liq) + vapour (V) (equivalent to ugandite lava) occurs at Fo2Di50Lc48 at 880 ± 5 °C. Phlogopite appears as the last phase at 830 ± 15 °C. The final crystalline assemblage of forsteritess + diopsidess + leucitess + phlogopite is similar to the phenocryst assemblage of missourite lava. Present study suggests that an olivine leucitite (ugandite) can be derived from an olivine italite, a slightly potassic peridotite and a leucitite magma.
A study of the join Fo–Di–Lc [P(H2O) = P(Total)] at 2.3 GPa shows that liquid compositions penetrate the primary phase volumes of forsteritess, phlogopitess, kalsilitess, K-feldsparss and diopsidess. It has the following three five-phase points: 1) one occurring at Fo9Di49Lc42 and 1005 ± 5 °C, where liquid and vapour coexists with forsteritess, phlogopitess and diopsidess (phlogopite-bearing madupite), 2) the second one at Fo4Di50Lc46 and 990 ± 10 °C, where diopsidess, K-feldsparss and phlogopitess coexist with liquid and vapour (pyroxene-bearing minette), and 3) the third one at Fo3Di21Lc76 and 775 ± 5 °C, where phlogopitess, kalsilitess and K-feldsparss are in equilibrium with liquid plus vapour (kalsilite-bearing minette).
The experimental results of the join Fo–Lc–åkermanite (Ak) show that the join 40 penetrates the primary phase volumes of forsteritess, phlogopitess, kalsilite, K-feldsparss, diopsidess and merwinitess. The data indicate the presence of four five-phase points: 1) one occurring at Fo7Lc42Ak51 and 1165 ± 5 °C, where phlogopitess, forsteritess, diopsidess coexists with liquid and vapour (olivine-bearing madupite), 2) the second one at Fo3Lc49Ak48 and 1140 ± 10 °C, where a liquid is in equilibrium with phlogopitess, K-feldsparss, diopsidess and vapour (pyroxene-bearing minette), 3) the third one at Fo18Lc21Ak61 and 1255 ± 10 °C, where merwinitess, forsteritess and diopsidess are in equilibrium with liquid and vapour (merwinite-bearing wherlite), and 4) the fourth one at Fo5Lc73.5Ak21.5 and 770 ± 5 °C, where kalsilitess, phlogopitess and K-feldspar coexist with liquid and vapour (kalsilite-bearing minette). The present data suggest that high pressure heteromorphic equivalent of a katungite magma is represented by a kalsilite-bearing minette, a pyroxene-bearing minette, or an olivine-bearing madupite. 相似文献
New evidence for high-pressure, eclogite facies metamorphism in the crystalline basement of the Tisza Megaunit (southern Hungary) is reported. The retrogressed mafic eclogite forms a small lens in the orthogneiss and it was found in the borehole near Jánoshalma. The carbonated eclogite contains the peak metamorphic assemblage omphacite + garnet + phengite + kyanite + clinozoizite + rutile + K-feldspar + quartz. Omphacite (Xjd0.40–0.41Xdio0.52–0.53Xhd0.05Xaug1.55–2.85) occurs in the matrix and as inclusions in garnet (Xpy0.37–0.38Xgrs0.21–0.22Xalm0.39–0.40Xsps0–0.01Xadr0–0.01) and kyanite. Thermobarometry based on net-transfer reactions between garnet, omphacite, kyanite and phengite yields P–T conditions of 710 ± 10 °C and 2.6 ± 0.75 GPa. Retrogression during decompression is manifested by formation of symplectites; the most typical are diopside + plagioclase after omphacite, corundum + spinel + plagioclase after kyanite and biotite + plagioclase after phengite. Carbonatization along the veins of the retrogressed eclogite was probably coeval with formation of these symplectites. At places where carbonate is absent the rock was completely hydrated and retrogressed down to the greenschist facies with the development of actinolite. Similar eclogites together with abundant orthogneisses occur mainly in the eastern parts of the Tisza Megaunit, suggesting the existence of an ancient (possibly Variscan) subduction/accretionary complex. 相似文献
A pressure-volume-temperature data set has been obtained for lawsonite [CaAl2Si2O7(OH)2.H2O], using synchrotron X-ray diffraction and an externally heated diamond anvil cell. Unit-cell volumes were measured to 9.4
GPa and 767 K by angle dispersive X-ray diffraction using imaging plates. Phase changes were not observed within this pressure-temperature
range, and lawsonite compressed almost isotropically at constant temperature. The P-V-T data have been analyzed using a Birch-
Murnaghan equation of state and a linear equation of state expressed as β=–1/V0 (∂V/∂P)T. At room temperature, the derived equation of state parameters are: K0=124.1 (18) GPa K'0 set to 4) and β–1=142.0(24) GPa, respectively. Our results are intermediate between previously reported measurements. The high-temperature
data show that the incompressibility of lawsonite decreases with increasing temperature to ∼500 K and then increases above.
Hence, the second order temperature derivative of the bulk modulus is taken into account in the equation of state; a fit of
the volume data yields K0=123.9(18) GPa, (∂K/∂T)P=–0.111(3) GPa K–1, (∂2K/∂T2)P=0.28(6) 10–3 GPa K–2, α0=3.1(2) 10–5 K–1, assuming K'0=4.
Received: 2 June 1998 / Revised, accepted: 12 Ocotber 1998 相似文献
Infrared absorption spectra of brucite Mg (OH)2 were measured under high pressure and high temperature from 0.1 MPa 25 °C to 16 GPa 360 °C using infrared synchrotron radiation
at BL43IR of Spring-8 and a high-temperature diamond-anvil cell. Brucite originally has an absorption peak at 3700 cm−1, which is due to the OH dipole at ambient pressure. Over 3 GPa, brucite shows a pressure-induced absorption peak at 3650 cm−1. The pressure-induced peak can be assigned to a new OH dipole under pressure. The new peak indicates that brucite has a new
proton site under pressure and undergoes a high-pressure phase transition. From observations of the pressure-induced peak
under various P–T condition, a stable region of the high-pressure phase was determined. The original peak shifts to lower wavenumber at −0.25 cm−1 GPa−1, while the pressure-induced peak shifts at −5.1 cm−1 GPa−1. These negative dependences of original and pressure-induced peak shifts against pressure result from enhanced hydrogen bond
by shortened O–H···O distance, and the two dependences must result from the differences of hydrogen bond types of the original
and pressure-induced peaks, most likely from trifurcated and bent types, respectively. Under high pressure and high temperature,
the pressure-induced peak disappears, but a broad absorption band between 3300 and 3500 cm−1 was observed. The broad absorption band may suggest free proton, and the possibility of proton conduction in brucite under
high pressure and temperature.
Received: 16 July 2001 / Accepted: 25 December 2001 相似文献
Pressure–temperature conditions of tourmaline breakdown in a metapelite were determined by high-pressure experiments at 700–900°C
and 4–6 GPa. These experiments produced an eclogite–facies assemblage of garnet, clinopyroxene, phengite, coesite, kyanite
and rare rutile. The modal proportions of tourmaline clearly decreased between 4.5 and 5 GPa at 700°C, between 4 and 4.5 GPa
at 800°C, and between 800 and 850°C at 4 GPa, with tourmaline that survived the higher temperature conditions appearing corroded
and thus metastable. Decreases in the modal abundance of tourmaline are accompanied by decreasing modal abundance of coesite,
and increasing that of clinopyroxene, garnet and kyanite; the boron content of phengite increases significantly. These changes
suggest that, with increasing pressure and temperature, tourmaline reacts with coesite to produce clinopyroxene, garnet, kyanite,
and boron-bearing phengite and fluid. Our results suggest that: (1) tourmaline breakdown occurs at lower pressures and temperatures
in SiO2-saturated systems than in SiO2-undersaturated systems. (2) In even cold subduction zones, subducting sediments should release boron-rich fluids by tourmaline
breakdown before reaching depths of 150 km, and (3) even after tourmaline breakdown, a significant amount of boron partitioned
into phengite could be stored in deeply subducted sediments. 相似文献