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1.
The paper discusses the results of mineralogical and petrographic studies of spinel lherzolite xenoliths and clinopyroxene megacrysts in basalt from the Jixia region related to the central zone of Cenozoic basaltic magmatism of southeastern China. Spinel lherzolite is predominantly composed of olivine (Fo89.6–90.4), orthopyroxene (Mg# = 90.6–92.7), clinopyroxene (Mg# = 90.3–91.9), and chrome spinel (Cr# = 6.59–14.0). According to the geochemical characteristics, basalt of the Jixia region is similar to OIB with asthenospheric material as a source. The following equilibrium temperatures and pressures were obtained for spinel peridotite: 890–1269°C and 10.4–14.8 kbar. Mg# of olivine and Cr# of chrome spinel are close to the values in rocks of the enriched mantle. It is evident from analysis of the textural peculiarities of spinel lherzolite that basaltic melt interacted with mantle rocks at the xenolith capture stage. Based on an analysis of the P–T conditions of the formation of spinel peridotite and clinopyroxene megacrysts, we show that mantle xenoliths were captured in the course of basaltic magma intrusion at a significantly lower depth than the area of partial melting. However, capture of mantle xenoliths was preceded by low-degree partial melting at an earlier stage.  相似文献   

2.
Optically homogeneous augite xenocrysts, closely associated with spinel–peridotite nodules, occur in alkali basalts from Hannuoba (Hebei province, China). They were studied by electron and X-ray diffraction to define the occurrence and significance of pigeonite exsolution microtextures. Sub-calcic augite (Wo34) exsolved into En62–62Fs25–21Wo13–17 pigeonite and En46–45Fs14–14Wo40–42 augite, as revealed by TEM through diffuse coarser (001) lamellae (100–300 Å) and only incipient (100) thinner ones (<70 Å). C2/c augite and P21/c pigeonite lattices, measured by CCD-XRD, relate through a(Aug)?a(Pgt), b(Aug)?b(Pgt), c(Aug)≠c(Pgt) [5.278(1) vs 5.189(1)Å] and β(Aug)≠β(Pgt) [106.55(1) vs 108.55(2)°]. Cell and site volumes strongly support the hypothesis that the augite xenocrysts crystallised at mantle depth from alkaline melts. After the augite xenocrysts entered the magma, (001) lamellae first formed by spinodal decomposition at a Tmin of about 1,100 °C, and coarsened during very rapid transport to the surface; in a later phase, possibly on cooling, incipient (100) lamellae then formed.  相似文献   

3.
Interaction between natural pargasite [Prg, SiO2 = 43.89 wt %, FeO/(FeO + MgO) = 0.35, (Na + K)A = 0.51] and H2O–NaCl fluid, whose composition (NaCl mole fraction) varied within the range X NaCl = NaCl/(NaCl + H2O) = 0–0.45, was experimentally studied in an internally heated apparatus at 900°C and 500 MPa. Natural pargasite begins to melt at a temperature 120–150°C lower than its synthetic analogue. In the presence of pure H2O, the subliquidus mineral assemblage involves amphibole Hbl 1, whose composition is closely similar to the starting Prg, clinopyroxene Cpx, calcic plagioclase Pl, and minor amounts of hercynite-magnetite spinel. With increasing X NaCl, the subliquidus assemblage systematically changed: calcic plagioclase disappeared and more Fe- rich amphibole Hbl 2 appeared at X NaCl = 0.07; Cpx disappeared at X NaCl = 0.14; and appearance of Na-Phl compositionally close to wonesite and almost complete disappearance of Hbl 1 was observed at X NaCl = 0.31. The composition of the melt also changed: its Na2O gradually increased (from 1.5 to 9–10 wt %), and CaO and SiO2 decreased(from 8.6 to 2 wt % and from 64 to 60 wt %, respectively, in recalculation to the anhydrous basis); at X NaCl ≥ 0.35, the melt was transformed from quartz- to nepheline-normative. The maximum Cl concentration of 1.2 wt % was measured in the melt poorest in SiO2. The experimental products contained spherical objects less than 10 μm in diameter that consisted of material that precipitated from the quenched fluid. These particles are richer than the melt in SiO2 (62–80 wt %) and poorer in Al2O3 (11–19 wt %) in experiments with X NaCl ≤ 0.24, but the differences between the compositions of the melt and particles decreased with increasing XNaCl. The relatively high concentrations of aluminosilicate material in the fluid is most likely explained by the high solubility of the melt in the fluid phase, with the formation in the fluid aqueous Si, Al–Si, Na–Al–Si, and other polymeric species. It is suggested that interaction of host rocks with such fluids, rich in granitic components, might be responsible for granitization (charnockitization) of mafic, and, particularly, ultramafic rocks described in the literature.  相似文献   

4.
A high-pressure single-crystal X-ray diffraction study has been carried out on a P21/c natural Mg-rich pigeonite sample with composition ca. Wo6En76Fs18 using a diamond anvil-cell. The unit-cell parameters were determined at 14 different pressures to 7.14 GPa. The sudden disappearance of the b-type reflections (h + k = odd) and a strong discontinuity (about 2.8%) in the unit-cell volume indicated a first-order P21/c–C2/c phase transition between 4.66 and 4.88 GPa. The P(V) data of the P21/c phase were fitted to 4.66 GPa by a third-order Birch–Murnaghan equation of state (BM3 EoS), whereas the limited number of experimental data collected within the C2/c phase between 4.88 and 7.14 GPa were fitted using the same equation of state but with K′ constrained to the value obtained for the P21/c fitting. The equation of state coefficients are V 0 = 424.66(6) Å3, K T0 = 104(2) GPa and K′ = 8(1) for the P21/c phase, and V 0 = 423.6(1) Å3, K T0 = 112.4(8) GPa, and K′ fixed to 8(1) for the C2/c phase. The axial moduli for a, b, and c for the P21/c phase were obtained using also a BM3-EoS, while for the C2/c phase only a linear calculation could be performed, and therefore the same approach was applied for comparison also to the P21/c phase. In general the C2/c phase exhibits axial compressibilities (β c > β a >> β b) lower than those of the P21/c phase (β b > β c ≈ β a; similar to those found in previous studies in clinopyroxenes and orthopyroxenes). The lower compressibility of the C2/c phase compared with that of the P21/c could be ascribed to the greater stiffness along the b direction. A previously published relationship between P c and M2 average cation radius (i.r.) has been updated using all the literature data on P21/c clinopyroxene containing large cations at M2 site and our new data. The following weighted regression was obtained: P c (GPa) = 26(4) ? 28(5) ×  i.r (Å), R 2 = 0.97. This improved equation can be used to predict the critical pressure of natural P21/c clinopyroxene samples just knowing the composition at M2 site.  相似文献   

5.
Ultramafic-mafic rocks from Makrirrakhi, Central Greece exhibit features of an original ophiolite sequence which contains depleted mantle material, ultramafic containing partial melt textures and possibly the mafic pluton which resulted from the coalescing of these partial melt segregations. Considerable mineralogical variation exists: unzoned olivine crystals range in composition from Fo78–84 (mafics) to Fo88–92 (ultramafics), plagioclases An64–79 (mafics) to An80–90 (ultramafics) and spinel varies from a chromian spinel (ultramafics) to a more aluminous-titaniferous spinel (mafics). Pyroxenes from the ultramafics display a limited range: En89–92 Fs9–8 Wo0–2 (orthopyroxene) and En48–54 Fs1–10 Wo38–50 (clinopyroxene). Mafic rocks display a greater range being richer in ferrosilite En36–65 Fs3–20 Wo33–51. Pyroxenes from within the partial melt segregations have chemical affinities with those from the gabbrotroctolite series. A model of partial melt within the upper mantle, and, a set of criteria to distinguish partial melt textures from cumulate textures, are developed from analytical data and textural evidence.  相似文献   

6.
The basaltic maar of Youkou, situated in the Adamawa Volcanic Massif in the eastern branch of the continental segment of the Cameroon Volcanic Line, contains mantle-derived xenoliths of various types in pyroclastites. Spinel-bearing lherzolite xenoliths from the Youkou volcano generally exhibit protogranular textures with olivine (Fo89.4?90.5), enstatite (En89???91Fs8.7?9.8Wo0.82?1.13), clinopyroxene, spinel (Cr#Sp?=?9.4–13.8), and in some cases amphibole (Mg#?=?88.5–89.1). Mineral equilibration temperatures in the lherzolite xenoliths have been estimated from three–two pyroxene thermometers and range between 835 and 937 °C at pressures of 10–18 kbar, consistent with shallow mantle depths of around 32–58 km. Trends displayed by bulk-rock MgO correlate with Al2O3, indicating that the xenoliths are refractory mantle residues after partial melting. The degree of partial melting estimated from spinel compositions is less than 10%: evidences for much higher degrees of depletion are preserved in one sample, but overprinted by refertilization in others. Trace element compositions of the xenoliths are enriched in highly incompatible elements (LREE, Sr, Ba, and U), indicating that the spinel lherzolites underwent later cryptic metasomatic enrichment induced by plume-related hydrous silicate melts. The extreme fertility (Al2O3?=?6.07–6.56 wt% in clinopyroxene) and the low CaO/Al2O3 ratios in the spinel lherzolites suggest that they could not be a simple residue of partial melting of primitive mantle and must have experienced refertilization processes driven by the infiltration of carbonatite or carbonated silicate melts.  相似文献   

7.
A. B. Vrevskii 《Petrology》2018,26(3):246-254
Numerical modeling of the generation and evolution of parental melts of the komatiite–tholeiite association of the Uraguba structure was carried out using previously obtained geochemical and isotope data. It was established that komatiite, komatiite and tholeiite basalts depleted in LREE and having εNd(Т = 2.79) = +2.9…+3.2 were generated by equilibrium partial melting (F > 15%) of a depleted source (garnet-bearing Ol0.63 + Opx0.22 + Cpx0.06 + Grt0.09 mantle peridotite) at 4–8 GPa, while the genesis of primary melts of LREE-enriched komatiites (LaN/SmN ~ 1.2–1.6) with εNd(Т = 2.79) = +2.5…+2.2 was related to the equilibrium partial melting (F > 20%) of an “enriched mantle peridotite” (EM–Ol0.60 + Opx0.20 + Cpx0.08 + Grt0.12) at pressure of 2.5–4 GPa. Coexistence in space and time of two types of melting products of mantle peridotites formed at different depths is explained by melting of different parts of adiabatically ascending mantle plume.  相似文献   

8.
Exsolution systems in synthetic pyroxenes were studied by transmission electron microscopy. An iron free sample En80Wo20 was prepared by devitrifying glass at 1300°C. Samples with bulk composition En50Fs30Wo20 and En35Fs38Wo27 were given various but well-defined heat treatments. The exsolution systems observed cannot unambiguously be related to the heat treatment. Periodic lamellar exsolution was observed parallel to (001) and (100) with sharp satellite reflections in the diffraction diagram. In more complex exsolution systems coarse (100) lamellae were found together with fine lamellae parallel to (001) and (100). An unusual phenomenon occurs at a (100) twin boundary where both individuals display exsolution lamellae parallel to (001). Pigeonite lamellae in one twin meet augite lamellae of the other individual at the twin boundary and vice-versa. The precise matching is achieved by a change in width near the boundary. Smoothly curved phase boundaries are developed in the obtuse angle of crosshatched (100) and (001) pigeonite lamellae in augite, whereas the boundaries in the acute angle are straight with sharp edges. This is consistent with elastic energy constraints.  相似文献   

9.
The isotopic systematics of noble gases (He and Ar) were studied in Neoarchean and Paleoproterozoic lower crustal xenoliths from the Belomorian mobile belt. The xenolith suite is dominated by garnet granulites (Grt + Cpx + Pl ± Opx ± Qtz ± Kfs ± Phl ± Hbl) and two-pyroxene or garnet pyroxenites (Cpx + Pl ± Grt ± Opx ± Hbl ± Qtz). The xenoliths and the host Devonian ultramafic lamprophyres forming diatremes and explosion dikes contain fluid with similar He and Ar isotopic compositions. It was found that the fluid was trapped by the rocks and xenolith minerals approximately simultaneously with the formation of the lamprophyres. This conclusion is based on the identical K-Ar ages of the majority of xenoliths and ultramafic lamprophyres. When the xenoliths were transported toward the surface by high-temperature ultrabasic melts, the noble gases occurring in them were partly (Ar) or completely (He) lost. The melts were contaminated by meteoric waters during their emplacement in the upper crust, which resulted in that the Ar isotopic composition of lamprophyres approached the composition of atmospheric Ar. The fluid phase that was liberated during melt crystallization severely affected the xenoliths, diminishing the difference between the isotope compositions of He and Ar in the xenoliths and ultramafic lamprophyres. The He isotope composition includes an admixture of mantle 3He, which is suggested by the high measured 3He concentrations, exceeding the calculated values, and high 3He/36Ar ratios in the xenoliths and their host lamprophyres. The fraction of the mantle component in the fluid trapped by the xenoliths was estimated as ～20%.  相似文献   

10.
The Kuznetsk Basin volcanic rocks are close in age (from 252.3 ± 0.6 to 246.2 ± 1.4 Ma) to the traps of the West Siberian Plate and Siberian craton, which formed as a result of the Permo-Triassic plume activity. The geologic and petrographic features evidence that the andesitic basalts exposed in the Karakan and Elbak quarries are effusive rocks; most of them are andesitic basalts, and the rest are trachyandesitic basalts. The mineral composition is as follows: olivine Fo59–66, plagioclase An47–60, and clinopyroxene En47–42Fs25–12Wo42–33; Mg# = 82–63. Using the COMAGMAT 3.5 program, the magma crystallization conditions during the andesitic-basalt formation were determined: 1109–1105 ºC, buffer QFM-NNO. The studied rocks are enriched in LREE ((La/Yb)ch = 4.7–7.5) and are depleted in HREE ((Sm/Yb)ch = 2.0–2.8). A specific geochemical feature of the rocks is strong Nb, Ta, Ti, and Eu negative anomalies ((La/Nb)PM = 4.5–1.6, (La/Ta)PM = 3.2–2.0, Eu/Eu? = 0.7) and a positive U anomaly on their normalized element patterns; ?Nd(T) varies from +2.3 to +3.1. The HREE depletion of the Kuznetsk Basin volcanic rock points to the presence of garnet in the mantle source during their generation. The low Mg# indicates that the parental melts are not of the primary-mantle genesis but are probably the product of differentiation in deep-seated intermediate magma chambers.  相似文献   

11.
Spinel-lherzolite xenoliths in alkali basalts from eastern China have porphyroclastic to equigranular textures displaying varying degrees of deformation and subsolidus re-equilibration. The proportions of minerals in these xenoliths vary from 52 to 72% homogeneous olivine (Fo88-91); 11 to 26% orthopyroxene (Wo0.9.1.6; En88-90; Fs8.7.10.7), with minor discontinuous variations of Al2O3, FeO, and CaO; 6 to 19% clinopyroxene (Wo43.47; En49.51; Fs3.7.6.7); and 1 to 5% spinel, with similar Mg# (79.6 to 82.6), but wider variations of Al2O3 and Cr2O3 (100Cr/(Cr + Al + Fe3+) = 8.1 to 23.6). Although previous trace-element and isotopic studies have shown that at least two distinctly different mantle sources were sampled by Cenozoic basalts, mineralogical heterogeneities seem to be minor within the spinel-peridotite-facies lithosphere beneath eastern China.

These xenoliths experienced limited interaction with the host basaltic magma during eruption. Symplectites of secondary, minute silicates, titanomagnetite, and sulfide have replaced orthopyroxene—and to a lesser extent olivine—at the contact with the basalt. The spinel in the margin of the xenolith is continuously zoned by substitutions of Fe3O4 (magnetite) and Fe2TiO4 (ulvospinel) for MgAl2O3 (spinel), and is rimmed by titanomagnetite with a sharp boundary. However, the compositions of the interior clinopyroxenes were commonly modified by metasomatic partial melting, which resulted in “spongy-textured” rinds on primary clinopyroxene. This secondary assemblage is composed mainly of a refractory, jadeite-poor clinopyroxene, which is largely in optica! continuity with the primary clinopyroxene in addition to interstitial feldspars, with minor titanomagnetite and Fe-Ni sulfides. This assemblage was produced by the introduction of K-rich fluids from the enclosing basaltic magma. The intensity of these secondary reactions appears to have been a function of the residence time of the xenolith in the host basalt. Therefore, all secondary alteration of both external and internal primary minerals in these xenoliths are the result of near-surface metasomatic processes, rather than of mantle phenomena.  相似文献   

12.
A unique clinopyroxene (En19Fs78Wo3), clinoeulite, space group P21/c, $${\text{(Fe}}_{{\text{1}}{\text{.48}}} {\text{Mg}}_{{\text{0}}{\text{.37}}} {\text{Mn}}_{{\text{0}}{\text{.08}}}^{{\text{2 + }}} {\text{Ca}}_{{\text{0}}{\text{.05}}} {\text{Al}}_{{\text{0}}{\text{.01}}} {\text{)}}_{{\text{1}}{\text{.99}}} {\text{ [Si}}_{{\text{2}}{\text{.01}}} {\text{O6],}}$$ contains sharp exsolution lamellae of ferroaugite (En17Fs43Wo40) from which the former presence of a ferropigeonite near En17Fs70Wo13 can be calculated. This two-pyroxene intergrowth is the main component of a eulysite containing also magnetite, olivine (Fo9Fa86Te5), quartz, oligoclase-K feldspar inter-growth, and retrograde cummingtonite with about 76 % grunerite end member. The occurrence of this most unusual rock type in the center of the Vredefort structure is attributed to a period of high-temperature metamorphism (at least 800 °–850 °C) which was followed by hot deformation of the rock during the Vredefort event thus probably preventing the common formation of orthopyroxene through pigeonite exsolution and inversion upon cooling. After this tectonic deformation, the rock recrystallized within the low-temperature stability range of clinoeulite to yield fine annealing textures. Late-stage equilibria at temperatures well below 500 °C include the complete unmixing of a former high-temperature anorthoclase, a Mg/Fe redistribution in the clinoeulite and olivine and, with the introduction of water, the partial formation of cummingtonite through reaction of clinoeulite, olivine, and quartz. During weathering the olivine was transformed to a nearly opaque, anhydrous ferrisilicate which, except for the change of Fe2+ to Fe3+ and the oxygen introduction, largely retained its original chemistry.  相似文献   

13.
Phenocryst and groundmass pyroxenes in 24 rocks of the tholeiitic, alkalic, and nephelinic suites from Haleakala and West Maui volcanoes, Maui, Hawaii, were analyzed quantitatively by electron microprobe. Results and conclusions: i) Tholeiites contain augite, pigeonite, and bronzite; alkalic rocks contain salite, augite, and ferroaugite; and nephelinic rocks have salite, sometimes of Wo>50 mole %. ii) The three suites can be distinguished by Ca contents of pyroxenes: High-Ca pyroxenes of tholeiitic rocks have Wo30–40; those of alkalic rocks have Wo38–48; and those of the nephelinic rocks have Wo47–51; i.e. Wo in clinopyroxene increases from tholeiitic, to alkalic, to nephelinic suites, iii). In the alkalic suite, rock types can be distinguished on the basis of clinopyroxene composition: Alkalic olivine and alkalic basalts have Wo38–45, hawaiites and mugearites have Wo45–48. Trachytes can be distinguished from both groups by higher Fe (Fs22–30) and Ca contents (Wo43–47). iv) Pyroxenes in tholeiitic rocks show higher intrarock variability (e.g. Fs12Wo40-Fs37Wo30) than those of the alkalic and nephelinic suites, v) Na2O bulk-rock content affects Na2O content of the precipitating high-Ca pyroxene; e.g. Na2O in groundmass pyroxene increases from tholeiitic, to alkalic (mafic members only), to nephelinic suites; a similar relationship is present within the differentiated alkalic suite, vi) In tholeiites, changes in groundmass high-Ca pyroxene compositions are related to changes in bulk rock compositions, e.g. FeO/FeO+MgO+CaO in clinopyroxene increases as this ratio increases in the bulk rock; this is not true for alkalic and nephelinic rocks, vii) In groundmass high-Ca pyroxene, Al2O3, Na20, and TiO2 contents increase and MnO content decreases with increasing Wo content from tholeiitic, to alkalic (mafic members only), to nephelinic suites, viii) Groundmass high-Ca pyroxenes are richer in MnO and Na2O and poorer in Cr2O3 compared to coexisting phenocrysts. High-Ca pyroxene phenocrysts in nephelinic rocks and in one mugearite are depleted in SiO2 and enriched in Al2O3 relative to coexisting groundmass clinopyroxene, indicating increased SiO2 activity during crystallization. Some tholeiites show the reverse; this Si—Al relationship is not clear in other samples.  相似文献   

14.
According to isotopic analysis of rocks of the Reft gabbro–diorite–tonalite complex (Middle Urals), gabbro and related diorite and dikes and vein-shaped bodies of plagiogranitoids, crosscutting gabbro, are similar to the depleted mantle substance in εNd(T) = 8.6–9.7 and εHf(T) = 15.9–17.9. Their model Hf ages are correlated with the time of crystallization. Here, the tonalites and quartz diorites constituting most of the Reft massif are characterized by lower values: εNd(T) = 3.7–6.0, εHf(T) = 11.1–12.7, and T DM values significantly exceeding the age datings. This is evidence that Neoproterozoic crustal rocks were a source of parental magma for these rocks. The primary 87Sr/86Sr ratio in rocks of both groups is highly variable (0.70348–0.70495). The data obtained allow us to reach the conclusion that the Reft gabbro–diorite–tonalite complex was formed as a result of nearly synchronous processes occurring in the crust and the mantle within a limited area.  相似文献   

15.
The Al-rich region of the CaO-MgO-Al2O3-SiO2 system was experimentally studied at pressures of 1.0–2.8 GPa and temperatures of 1300–1535°C. The slopes of the lines of the monovariant reactions An + Sp = Cpx + Cor + (Ga) and L = Cpx + Ga + Cor + Sp and the compositions of the phases involved in these reactions are determined. The results are utilized in the topological analysis of the aluminous region of the CaO-MgO-Al2O3-SiO2 system. On this basis, the principal structure of the phase diagram is analyzed, and a phase diagram is constructed for the junction region of the quaternary system and the CaO-Al2O3-SiO2 ternary system. A continuous series of the monovariant eutectic: L = Cpx + Opx + Fo + An, L = Cpx + Opx + An + Sp, L = Cpx + (Ga) + An + Sp, L = Cpx + Cor + (Ga) + An, L = An + Ga + Cpx + Ky and L = Ga + Cpx + Ky + Qz is examined within the pressure range from atmospheric to 3.0 GPa and higher. Analogous “telescoped” eutectic series are of fundamental character for interpreting the evolution of magmatic melts. A physicochemical model is suggested for the evolution of magmatic melts that produce rocks of the calc-alkaline series, with this model underlain by the fact that a change in the composition of magmatic melt at a pressure decrease should correspond to the minimum melting temperatures, i.e., to melts in the fundamental series of eutectic reactions. The comparison of our physicochemical model and rocks of the calc-alkaline series shows that the compositions of rocks of the calc-alkaline series are close to the compositions determined for the eutectic equilibria, and the mineralogical composition of xenoliths and megacrysts in volcanic and dike varieties of the rocks are similar to the subsolidus phases of the established fundamental eutectic system.  相似文献   

16.
The rift system of the Dnieper–Donets trough (DDT) is the largest magmatic area in the East European Platform. Basalts of the Voronezh Crystalline Massif (VCM) are spatially constrained to the eastern shoulder of DDT and occur far away (at a distance of 150–200 km) from the rift axis. The rocks are hosted in the Paleoproterozoic Vorontsovskii terrane and are grouped in a few fields within an area of 200 × 100 km. Basalts at most of the fields were erupted at the boundary between mid- and late Frasnian time in the Late Devonian and can be studied exclusively in core material recovered by boreholes. Newly obtained mineralogical, geochemical, and isotopic-geochemical data show that the Devonian volcanic rocks in VCM are tholeiites (Bas) and basaltic andesites/andesites (ABas). The geological section was examined most exhaustively in the Novokhopersk area (Borehole 175). The bottom of the vertical section is made up of basaltic andesites and andesites (ABas) (thickness 34 m), which rest on an eroded surface of late Frasnian sandstones. The rocks are overlain by a thin (8 m thick) tholeiite sheet (Bas2), which gives way to ABas (13 m) upsection. The top portion of the vertical section is composed of tholeiites with petrography and geochemical evidence of crustal contamination (Bas1) (apparent thickness 5 m). Geochemical parameters of Bas (mg# 42–52 at SiO2 47–51 wt %) are typical of continental tholeiites. The rocks have (87Sr/86Sr)0 = 0.7043–0.7048 and εNd(372) = 2.1–3.5. ABas (mg# 28–31 at SiO2 52–60 wt %) are enriched in Y (48 ppm), and possess Nb/Nb* = 0.7–0.8 and high Zn/Cu = 1.9–2.3. The rocks have (87Sr/86Sr)0 = 0.7034–0.7048 and Nd–εNd(372) = 0.1. Some portions of Bas melts assimilated the upper crustal material, which was similar to Paleoproterozoic granites, and ABas are contaminated in the lower crust with derivatives of Early Cambrian alkaline mafic melts. Petrographic data and simulations of fractional crystallization show that olivine and high-Mg clinopyroxene were the first to crystallize from the melt. After this, clinopyroxene and plagioclase simultaneously crystallized at temperatures from 1070 to 1020°C in Bas and at 1040–900°C at f O2 below QFM + 1 in ABas. The source of ABas was likely a network of hornblendite or amphibole pyroxenite veins in peridotite in the lithospheric mantle or amphibolized peridotite cumulate in an underplating zone; and Bas were derived from spinel peridotites of an asthenospheric diapir. The setting of the basalts relative to the DDT axis and the asymmetric zoning of magmatism in DDT (with kimberlites and other deep rocks constrained to the western shoulder and tholeiites occurring in the axial part of the rift and its eastern shoulder) can be explained by the model of an asymmetric rift structure with a translithospheric detachment gently dipping beneath VCM.  相似文献   

17.
The relative plume thermal power Ka = N/N1 is used (N is the thermal power transferred from the plume base to its conduit and N1 is the thermal power transferred from the plume conduit into the surrounding mantle in the steady-state heat conduction regime). Thermochemical mantle plumes with small (Ka < 1.15) and intermediate (1.15 < Ka < 1.9) thermal powers are formed at the core–mantle boundary beneath cratons in the absence of horizontal free-convection mantle flows beneath them, or in the presence of weak horizontal mantle flows. Thermochemical plumes reach the Earth’s surface when their relative thermal power is Ka > 1.15. The thermal and hydrodynamical structure of the plume conduit ascending from the core–mantle interface to the level from which the magmatic melt erupts on the Earth’s surface is presented. The model of two-stage eruption of the melt from the plume conduit to the surface is considered. The critical height of the massif above the plume roof, at which the eruption conduit supplying magmatic melt to the surface forms, is determined. The volume of melt erupting through the eruption conduit to the surface is estimated. The dependence of depth Δx from which the melt is transported to the surface on the plume diameter for a kinematic viscosity of ν = 0.5–2 m2/s is presented. In the case when the value Δx is larger than the depth starting from which diamond is stable (150 km), the melt from the plume conduit can transport diamonds to the Earth’s surface. The melt flow in the eruption conduit is considered as a turbulent flow in a cylindrical duct. The velocity of the melt flow in the eruption conduit and the time for the melt to be transported to the surface from a depth of Δx = 150 km for a kinematic viscosity of the melt in the eruption conduit νv = 0.01–1 m2/s are determined. Tangential stress on the eruption conduit sidewall is estimated in cases of melt flow both in smooth and rough conduits.  相似文献   

18.
Absorption of the synchrotron emission of the quasar 3C 345 in the continuum and H(93–95)α and H(78–79)α radio recombination lines is studied. The upper limit for absorption in the H(93–95)α lines is Tal/Tac < 0.7%; absorption in the H(78–79)α lines with antenna temperature Tal = 25 mK, linewidth Δf = 5.3 ± 0.08 MHz, and Tal/Tac ≥ 0.3% has been detected. A correction to the redshift Δz = 0.00135 ± 0.00008 (z = 0.59365) has been determined.  相似文献   

19.
Pyroxenes of general stoichiometry Mg(Ge x Si1?x )O3 were encountered in attempts to synthesise Ge-substituted talcs at 0.2 GPa, 650–700 °C. Orthopyroxenes (Pbca) of compositions x = 0.21, 0.30, and 0.34 were identified, and also a P21/c clinopyroxene of composition x = 0.63, and C2/c clinopyroxenes of compositions x = 0.91 and 1. End-member clinoenstatite MgSiO3-P21/c synthesised at 16 GPa, 1300 °C and transformed from C2/c was also included in the study. Crystal structure refinements using single-crystal XRD data showed that unit-cell parameters vary linearly with Si–Ge for the Pbca and P21/c pyroxenes, both of which have two symmetrically non-equivalent tetrahedral chains. Refinement of Si–Ge occupancies at tetrahedral sites showed that the two chains of all primitive pyroxenes have very different compositions, with XGe(TB) ? XGe(TA). This difference arises from the greater flexibility of the B-chain to rotate in response to tetrahedral expansion due to increasing Ge content. The TA-M2 shared polyhedral edge imposes significant constraints on the flexibility of the A-chain, which can accommodate much less Ge than the B-chain. Linear trends of cell parameters, site occupancies, and structural parameters for the primitive pyroxenes, when extrapolated to published data for MgGeO3–Pbca, extend across the entire Si–Ge join.  相似文献   

20.
The crystallization of plagioclase-bearing assemblages in mantle rocks is witness of mantle exhumation at shallow depth. Previous experimental works on peridotites have found systematic compositional variations in coexisting minerals at decreasing pressure within the plagioclase stability field. In this experimental study we present new constraints on the stability of plagioclase as a function of different Na2O/CaO bulk ratios, and we present a new geobarometer for mantle rocks. Experiments have been performed in a single-stage piston cylinder at 5–10 kbar, 1050–1150?°C at nominally anhydrous conditions using seeded gels of peridotite compositions (Na2O/CaO?=?0.08–0.13; X Cr = Cr/(Cr?+?Al)?=?0.07–0.10) as starting materials. As expected, the increase of the bulk Na2O/CaO ratio extends the plagioclase stability to higher pressure; in the studied high-Na fertile lherzolite (HNa-FLZ), the plagioclase-spinel transition occurs at 1100?°C between 9 and 10 kbar; in a fertile lherzolite (FLZ) with Na2O/CaO?=?0.08, it occurs between 8 and 9 kbar at 1100?°C. This study provides, together with previous experimental results, a consistent database, covering a wide range of P–T conditions (3–9 kbar, 1000–1150?°C) and variable bulk compositions to be used to define and calibrate a geobarometer for plagioclase-bearing mantle rocks. The pressure sensitive equilibrium:
$$\mathop {{\text{M}}{{\text{g}}_{\text{2}}}{\text{Si}}{{\text{O}}_{\text{4}}}^{{\text{Ol}}}}\limits_{{\text{Forsterite}}} +\mathop {{\text{CaA}}{{\text{l}}_{\text{2}}}{\text{S}}{{\text{i}}_{\text{2}}}{{\text{O}}_{\text{8}}}^{{\text{Pl}}}}\limits_{{\text{Anorthite}}~} =\mathop {{\text{CaA}}{{\text{l}}_{\text{2}}}{\text{Si}}{{\text{O}}_{\text{6}}}^{{\text{Cpx}}}}\limits_{{\text{Ca-Tschermak}}} +{\text{ }}\mathop {{\text{M}}{{\text{g}}_{\text{2}}}{\text{S}}{{\text{i}}_{\text{2}}}{{\text{O}}_{\text{6}}}^{{\text{Opx}}}}\limits_{{\text{Enstatite}}} ,$$
has been empirically calibrated by least squares regression analysis of experimental data combined with Monte Carlo simulation. The result of the fit gives the following equation:
$$P=7.2( \pm 2.9)+0.0078( \pm 0.0021)T{\text{ }}+0.0022( \pm 0.0001)T{\text{ }}\ln K,$$
$${R^2}=0.93,$$
where P is expressed in kbar and T in kelvin. K is the equilibrium constant K?=?a CaTs × a en/a an × a fo, where a CaTs, a en, a an and a fo are the activities of Ca-Tschermak in clinopyroxene, enstatite in orthopyroxene, anorthite in plagioclase and forsterite in olivine. The proposed geobarometer for plagioclase peridotites, coupled to detailed microstructural and mineral chemistry investigations, represents a valuable tool to track the exhumation of the lithospheric mantle at extensional environments.
  相似文献   

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