The TiO2–K2O–P2O5 diagram: A method of discriminating between oceanic and non-oceanic basalts

The TiO₂–K₂O–P₂O₅ ternary diagram is proposed as a method of discriminating between oceanic and non-oceanic (continental) basalts. This diagram is effective for non-alkaline “primitive” basalts: fractionated rocks cannot be adequately discriminated. Suitable analyses are those which have total alkalies ≤ 20% in an (Fe₂O₃ + FeO)–MgO–(Na₂O + K₂O) diagram. The proposed dividing line separates 93% of 222 ocean-floor and ocean-ridge basalts into the oceanic field and > 80% of continental basalt analyses into the non-oceanic field. Two exceptions are the Tertiary basalts of Greenland and the Deccan Traps which have oceanic affinities. “Continental” suites displaying an oceanic affinity in the TiO₂–K₂O–P₂O₅ diagram may be a result of abortive attempts to generate new sea floor. Preliminary results for dike swarms and Archean basalts suggest preponderant oceanic affinities. Alteration and metamorphism of oceanic basalts generally occasion enrichment of K₂O relative to TiO₂ and P₂O₅.     

The petrochemistry of ophiolite gabbroic complexes. A key for the classification of ophiolites into low-Ti and high-Ti types

Ophiolites have been divided into two groups: high-Ti and low-Ti types. These can be discriminated by studying the fractionation trends of both gabbroic complexes (this work) and lavas and dykes [16], particularly in the TiO₂/M.I. diagram. The first type typically shows MORB-like magmas whereas in the second the magma types have a spectrum of composition from mid-ocean ridge basalts to island arc tholeiites and boninite-like magmas often occur.High-Ti ophiolites are petrologically and geochemically similar to major oceanic and ensialic back-arc basin crusts as well as oceanic crust generated during the intermediate and late-stage opening of intraoceanic back-arc basins.Parental magmas and fractionation processes of low-Ti ophiolites fit with an hypothesis of their formation in the early stage of opening of intraoceanic back-arc basins.     

Geological setting of basaltic rocks in an accretionary complex,Khangai–Khentei Belt,Mongolia

We describe the mode of occurrence and geochemical characteristics of basalts, in the Khangai–Khentei belt in Mongolia, overlain by Middle Paleozoic radiolarian chert in an extensive accretionary complex. These basalts are greatly enriched in K, Ti, Fe, P, Rb, Ba, Th, and Nb in comparison to the composition of the mid‐ocean ridge basalts, indicative of within‐plate alkaline type. Ti/Y vs Nb/Y and MnO/TiO₂/P₂O₅ ratios of the basalts also suggest within‐plate affinities. Considering the geochemical characteristics as well as the conformable relationship with the overlying radiolarian chert, the alkaline basalts were clearly not continental but formed a pelagic oceanic island. The mode of occurrence and geochemistry of the basalts show that the alkaline basaltic volcanic activity had taken place to form an oceanic island in the Paleozoic pelagic region sufficiently far from continents to allow radiolarian ooze accumulation.     

Fractionation of abyssal tholeiites: Samples from the oceanographer Fracture Zone (35°N, 35°W)

Chemical analyses of 48 fresh abyssal tholeiite specimens sampled from two dredge localities clearly define systematic chemical differences which indicate a moderate iron-enrichment trend of fractionation oblique to the FeO^*₂O, P₂O₅ and TiO₂. These results suggest that fractionation may be important in controlling the chemistry of abyssal tholeiites along sections of the mid-oceanic ridge.     

Estimates of possible diffusional effects in trace element separations

Igneous material dredged from the Rio Grande rise, South Atlantic Ocean, includes basaltic rocks, some having mafic nodules and megacrysts, and volcanic breccias composed largely of basaltic fragments. These samples represent the only volcanic rocks recovered from this aseismic rise. Bulk compositions show alkalic basalt, trachybasalt, and trachyandesite; the rock types are similar to those of nearby Tristan da Cunha, Gough, and the Walvis ridge. Microprobe analyses show basaltic groundmass to have olivine, Fo₈₅, pyroxene, Fs₁₃Wo₄₆, feldspar, An₇₁, plus interstitial alkali feldspar. Mafic nodules and megacrysts have olivine, Fo_86–90 and pyroxene Fs_6–7.5Wo_45–46; Al₂O₃ 2.5–4 wt.%.The Rio Grande rise rocks have compositional characteristics of an alkalic basaltic suite, and not of mid-ocean ridge tholeiite. Based on mineral compositions, nodules and megacrysts in basalt are interpreted as cognate inclusions. Because oceanic alkalic basaltic rocks are almost invariably associated with islands and seamounts, the Rio Grande rise probably represents a series of alkalic-basalt islands that formed and eventually subsided during rifting of the South Atlantic; the dredged volcanic breccias are probably slump deposits from those volcanoes. This interpretation lends support to the Rio Grande rise having formed at a hot spot, but the possibility of alkalic rocks having formed along fracture zones should not be discounted.     

An outline of the geology and geochemistry,and the possible petrogenetic evolution of the volcanic rocks of the Tonga-Kermadec-New Zealand island arc

The Pleistocene-Recent volcanism of this arc extends nearly linearly NNE from northern New Zealand for some 2800 km. Along its western margin lies an active marginal basin (Lau Basin and Havre Trough) which has its southern termination in the Taupo volcanic zone (TVZ, New Zealand). The New Zealand arc segment is developed within a continental crust, whereas the Tonga-Kermadec segments are developed on a ridge system within the oceanic basin. Submarine morphology suggests that the Kermadec volcanoes represent a less advanced stage of evolution relative to those of Tonga.Magmas erupted within the TVZ are dominantly rhyolitic (≈16,000 km³) with subordinate andesites and rare high-alumina tholeiites and dacites. The Kermadec Islands are dominated by tholeiites and basaltic andesites, with subordinate andesites and dacites. The Tongan Islands are dominated by basaltic andesites, with locally developed andesites and dacites. These Tonga-Kermadec lavas are characterised by subcalcic groundmass clinopyroxenes, whereas the younger group of TVZ andesites contain groundmass hypersthene and augite.Geochemically, the TVZ andesites are systematically enriched (relative to those of Tonga-Kermadec) in “incompatible” elements (e.g. K, Rb, Cs, Ba, light REE, U, Th, Zr, Pb), are less Fe-enriched, and contain more radiogenic Sr and Pb (excepting certain ²⁰⁷Pb/²⁰⁴Pb compositions). The evidence points to crustal equilibration of the TVZ andesites prior to eruption.A complete overlap of major and trace element chemistry (including TiO₂) is observed between the Kermadec-TVZ tholeiites and basaltic andesites, and the ocean floor tholeiites of the Lau Basin. Compared to the Tongan lavas, those of the Kermadecs exhibit a greater degree of chemical variability, also reflected in the greater heterogeneity in their Pb isotopic compositions. Moreover, many of the Tonga-Kermadec basaltic andesites exhibit more depleted “incompatible” trace element abundances than the Kermadec and TVZ tholeiites.The “primary” magmas of this arc are interpreted to be of basaltic andesite type, derived from Benioff zone melting (essentially anhydrous), but extensively modified by low-pressure crystal fractionation processes. The Kermadec tholeiites are explained as products of relatively shallow upper mantle partial fusion induced during the earlier stages of diapiric rise of Benioff zone-derived magmas, which are sufficiently hot to intersect the peridotite solidus. This should result in the production and intermixing of a series of magmas extending from olivine tholeiite to basaltic andesite composition. The voluminous rhyolites of TVZ are interpreted as the products of crustal fusion involving Mesozoic sediments.     

Mineralogy and chemistry of modern orogenic lavas — some statistics and implications

Island arc and continental margin (i.e. western Americas) lavas are divided (based on raw data from literature) into basalts (defined by absence of Ca-poor pyroxene, dominated by quartz-normative tholeiites); basaltic andesites and andesites (subdivided on basis of breaks in SiO₂ histogram and taken as <56% and 56–63% SiO₂; Ca-poor pyroxene present; amphibole and biotite absent); and hornblende (±biotite) lavas, which prove to be mainly relatively silicic andesites. Relative proportions of these types are (576 samples): 23% basalts, 29% basaltic andesites; 30% andesites; 18% hornblende andesites. The compilation emphasizes the dominance of calcic plagioclase (labradorite-anorthite) amongst the phenocryst phases. Pyroxenes are largely augite and hypersthene (En_60–75); olivine (Fo_65–85) is common through all compositions. There is an overall close similarity in chemistry and mineralogy between continental margin and island arc lavas, although small consistent differences are apparent (e.g. K₂O, TiO₂, P₂O₅).Modal data indicate that 70% of lavas are phenocryst-rich (20–60 vol.%), and that phenocryst contents show a bimodal distribution. Statistically and petrologically significant correlations are found between mineralogy and rock chemistry, most notably between total rock Al₂O₃ and modal phenocrystic plagioclase (found in all data groups, except hornblende andesites). This, and related data and correlations, indicate that the majority of orogenic magmas are modified by crystal fractionation (including crystal accumulation) processes dominated by plagioclase, and interpreted to occur under relatively low pressures. Dominance of plagioclase suggests phenocryst precipitation occurs typically in water-undersaturated magmas.     

Volcanism in the Sumisu Rift, I. Major element, volatile, and stable isotope geochemistry

A bimodal volcanic suite with KAr ages of 0.05–1.40 Ma was collected from the Sumisu Rift using alvin. These rocks are contemporaneous with island arc tholeiite lavas of the Izu-Ogasawara arc 20 km to the east, and provide a present day example of volcanism associated with arc rifting and back-arc basin initiation. Major element geochemistry of the basalts is most similar to that of basalts found in other, more mature back-arc basins, which indicates that back-arc basins need not begin their magmatic evolution with lavas bearing strong arc signatures.Volatile concentrations distinguish Sumisu Rift basalts from island arc basalts and MORB. H₂O contents, which are at least four times greater than in MORB, suppress plagioclase crystallization. This suppression results in a more mafic fractionating assemblage, which prevents Al₂O₃ depletion and delays the initiation of Fe₂O_3^(tot) and TiO₂ enrichment. However, unlike arc basalts,Fe^3+/ΣFe ratios are only slightly higher than in MORB and are insufficient to cause magnetite saturation early enough to suppress Fe₂O_3^(tot) and TiO₂ enrichment. Thus, major element trends are more similar to those of MORB than arcs.H₂O, CO₂ and S are undersaturated relative to pure phase solubility curves, indicating exsolution of an H₂O-rich mixed gas phase. HighH₂O/S, highδD, and low (MORB-like)δ³⁴S ratios are considered primary and distinctive of the back-arc basin setting.     

Oxygen isotope variations in marginal basin and ocean-ridge basalts

Oxygen isotope analyses have been made on 27 tholeiitic basalts from the Lau and Mariana marginal ocean basins and from mid-ocean ridges. The ¹⁸O values are related to the extent of hydration by submarine weathering as indicated by H₂O^? and total water content. Extrapolation to zero H₂O^? content gives a δ¹⁸O value of 5.5‰ on the SMOW scale for unaltered marginal basin basalts, in exact agreement with the oxygen isotope “signature” of ocean-ridge tholeiites. Three alkali basalts from seamount provinces also fit the tholeiite relationship. A Lau Basin gabbro has the tholeiitic ¹⁸O content, but an Indian Ocean gabbro is unusually light (δ¹⁸O = 4.0 for whole rock, plagioclase, and amphibole), and resembles the low -¹⁸O Iceland basalts. The basalt data confirm petrologic and chemical evidence for origin of marginal basins by extensional processes with production of basalts from depleted mantle material isotopically identical to the source of ocean-ridge tholeiites.     

Subdivision of the Archean lavas of the Abitibi area,Canada, from Fe-Mg-Ni-Cr relations

The lavas of a part of the Archean Abitibi region may be divided into three stratigraphic levels in each of which FeO-MgO-Ni-Cr contents conform to certain broad differentiation trends. Within each stratigraphic level, there is a tendency for rocks to become more felsic upwards. The earliest and stratigraphically lowest subdivision is composed largely of magnesium-rich basaltic lavas called the magnesian suite. In the central part of the pile, where basalts predominate, the lavas contain intermediate MgO concentrations, and display pronounced Fe enrichment in intermediate members similar to conventional tholeiites. In the latest and stratigraphically highest lavas, where andesites predominate, Fe depletion is characteristic; these lavas are grouped into a primitive calcalkaline suite. All of the Abitibi lavas contain unusually high Ni and Cr. Other Archean lava piles appear to be similarly divisible, although all three suites are not always present.Mafic end-members of the three complete differentiation suites are viewed as possible source magmas derived by partial melting in a primitive, olivine-rich parent, probably the Archean mantle. The earliest, and highest temperature magmas precipitated olivine, Al-clinopyroxene, and minor Al-orthopyroxene, and display moderate FeO, TiO₂, MnO, Al₂O₃, and CaO enrichment in more felsic members. The intermediate age lavas, derived originally by less complete melting in the parent, precipitated plagioclase, olivine, and lesser clinopyroxene, and display, as a result, strong Fe enrichment until, in intermediate members, magma volumes became small enough to yield P_f of levels sufficient to form clinopyroxene plus magnetite. The uppermost lavas, derived by relatively small volumetric melting in the parent, contain abundant Fe-Ti oxides in even the most mafic members, along with augite and plagioclase.     

Mineral chemistry and petrogenesis of chromitites from the Khoy ophiolite complex,Northwestern Iran: Implications for aggregation of two ophiolites

The Khoy ophiolitic complex in Northwestern Iran is a part of the Tethyan ophiolite belt, and is divided into two sections: the Eastern ophiolite in Qeshlaq and Kalavanes (Jurassic–Cretaceous) and the Western ophiolite in Barajouk, Chuchak and Hessar (Late Cretaceous). Our chromitites can be clearly classified into two groups: high‐Al chromitites (Cr# = 0.38–0.44) from the Eastern ophiolite, and high‐Cr chromitites (Cr# = 0.54–0.72) from the Western ophiolite. The chromian spinels in high‐Al chromitite include primary mineral inclusions mainly as Na‐bearing diopside and pargasite with subordinate rutile and their formation was probably related to reaction between a MORB (mid‐ocean‐ridge basalt)‐like melt with depleted harzburgite, possibly in a back‐arc setting. Their host harzburgites contain clinopyroxene with higher contents of Al₂O₃, Na₂O, Cr₂O₃, and TiO₂ relative to Western harzburgites and are possibly residue after moderate partial melting (~15 %) whereas the Western harzburgite is residue after high partial melting (~25 %). The chromian spinel in the Western Khoy chromitites contains inclusions such as clinopyroxene, olivine and platinum group mineral‐bearing sulfides. These Western chromitites were possibly formed at two stages during arc growth and are divided into the moderately high‐Cr# chromitites (Barajouk and Hessar) and the high‐Cr# chromitites (Chuchak A and C). The former crystallized from island‐arc‐tholeiite (IAT) melts during reaction with the host depleted harzburgites, whereas the latter crystallized from boninitic melts (second stage melt) during reaction with highly depleted harzburgite in a supra‐subduction‐zone environment. Based on the mineral chemistry of chromian spinels, pyroxenes, and mineral inclusions, the chromitites and the host peridotites from the Eastern and Western Khoy ophiolites were formed in a back‐arc basin and arc‐related setting, respectively. The Khoy ophiolitic complex is a tectonic aggregate of the two different ophiolites formed in two different tectonic settings at different ages.     

The relationship between major element chemistry and tectonic environment of basic and intermediate volcanic rocks

This work reports the preliminary results of a study of the relationship between tectonic environment and major element chemistry of volcanic rocks. Using a file of 8400 analyses of rocks of varying ages and geographic distribution it has been found that a simple ternary plot of MgOFeO(total)Al₂O₃ may be used to distinguish five tectonic environments: ocean ridge and floor, ocean island, continental, orogenic, and spreading center island. Subalkaline “basaltic-andesites” (51–56% SiO₂ calculated anhydrous) are used in this study. Alkaline rocks do not generally show the simple patterns of tholeiitic or subalkaline rocks. The ocean island suite is bimodal with one mode tholeiitic and the other alkaline. A bimodal age/chemistry relationship in the continental suite is tentatively related to different conditions during and after active breaking up of continents (rifting and drifting stages).Most of the Archean rocks in our file generally do not fall in the orogenic field. It is unlikely that modern island arc models can be generally applied to Archean greenstone belts. Locally, however, there may be Archean rocks analogous in some respect to modern calc-alkali rocks.     

Mineralogical and geochemical study of a newly discovered mafic granulite, northwest China: Implications for tectonic evolution of the Altay Orogenic Belt

Abstract A mafic granulite body was newly discovered in the Altay Orogenic Belt, northwest China. The rocks comprise a suite of coarse‐grained and fine‐grained granulites. Orthopyroxenes (hypersthenes) in the rocks have high X_Mg and low Al₂O₃ contents, whereas clinopyroxenes have low TiO₂ and Al₂O₃ contents. Amphiboles and biotites have a high Mg/(Mg + Fe²⁺) ratio and low contents of F and Cl. The peak metamorphic pressure–temperature (P–T) conditions are estimated as 750–780°C and 6–7 kbar, and retrograde P–T conditions are in the range of 590–620°C and 2.3–3.7 kbar, indicating significant decompression. Metamorphic reactions and P–T estimates define a clockwise P–T path. Geochemically, the rocks are high in Mg/(Mg + Fe) and Al₂O₃, depleted in U, Th, K and Rb, and characterized by light rare earth element enrichment and a weak positive Eu anomaly. The Altay mafic granulite shows depleted Nb, P and Ti contents in the mid‐oceanic ridge basalt normalized spider diagram. The geochemical characteristics suggest that the protolith of the Altay mafic granulite was calc‐alkaline basalt and andesite with an island‐arc affinity. The rock has a high ¹⁴³Nd/¹⁴⁴Nd ratio with ?Nd(0) > 0, indicating derivation from a mantle‐depleted source. In the present study, a two‐stage model for the evolution of the Altay mafic granulite is proposed: an early stage in which calc‐alkaline basalt and andesite with island‐arc affinity were subducted into a deeper level of the crust and subjected to granulite‐facies metamorphism generating the mafic granulite, followed by the later stage exhumation of the system into the upper crust by the late Paleozoic thrusting.     

Basalt-andesite-rhyolite-H2O: Crystallization intervals with excess H2O and H2O-undersaturated liquidus surfaces to 35 kolbras,with implications for magma genesis

Three rocks representing the calc-alkaline rock series gabbro-tonalite-granite or basalt-andesite-rhyolite were reacted with varying percentages of water in sealed capsules between 600 and 1300°C and pressures to 36 kbars, corresponding to depths of more than 120 km within the earth. For each rock we present complete P-T diagrams with excess water, and the water-undersaturated liquids surface projected from P-T-X_H2O space mapped with contours for constant H₂O contents and with the fields for near-liquidus minerals. All changes in liquidus and solidus slopes can be correlated with changes in mineralogy from less dense to more dense, or with expansion of crystallization fields, without appeal to changes in molar volume of H₂O in liquid and vapor phases. The results indicate that tholeiites and andesites of the calc-alkaline series with compositions similar to the rocks studied are not primary magmas from mantle peridotite at depths greater than about 50 km. Primary andesitic magmas from shallower levels would require very high water contents and we do not believe such magmas could normally reach the surface. The liquids results are consistent with the derivation of andesites with little dissolved water as primary magmas from subducted ocean crust (quartz eclogite), but multi-stage models are preferred. Temperatures required for the generation of andesites by fusion of continental crust are higher than considered reasonable. The evidence precludes the generation of primary rhyolites or granites from the mantle of subducted oceanic crust at mantle depths. Primary rhyolite or granite magmas with moderate water contents (saturated or undersaturated) can be generated in the crust at reasonable temperatures, and could reach near-surface levels before vesiculation. Water-undersaturated granite liquid with residual crustal minerals could constitute plutonic magmas of intermediate composition.     

Glass inclusions as samples of early magmatic liquid: determinative method and application to a south atlantic basalt

Silicate melt inclusions in phenocrysts are not directly representative of trapped magmatic liquid because chemical interaction between inclusions and host crystals usually occurs after melt entrapment. However, if more than one phenocryst type in a suite of rocks contains melt inclusions, the original trapped-liquid composition can be accurately fixed by the intersection of host-mineral fractionation lines in a triangular oxide plot of inclusion analyses. When plotted on a CaO—MgO—Al₂O₃ triangular diagram, analyses of inclusions in plagioclase, olivine, and clinopyroxene from a basalt dredged off Bouvet Island fall along crystal fractionation lines that intersect at a single point. This point represents an initial trapped liquid composition rich in CaO and MgO, and low in TiO₂ and total alkalies. The composition is transitional between tholeiite and basaltic komatiite, and may be indicative of extensive melting of clinopyroxene in the mantle.     

Great-circle Rayleigh wave attenuation and group velocity,Part IV: Regionalization and pure-path models for shear velocity and attenuation

Pure-path averages for group velocities and specific attenuation have been calculated from individual observations and from path averages for two regionalizations; one original to this study and the other previously devised by Wu. Both are based on four upper-mantle provinces: ocean basin, continent, island arc and mid-ocean ridge. Pure-path group velocities and specific attenuation have also been calculated for combinations of regions and provide well separated regional measurements for such composite regions.Shear-velocity models for pure and combined regions have been derived by a controlled Monte Carlo inversion procedure and indicates that a low-velocity zone is required beneath the oceans, but is not required beneath continents. Models have been produced for pure and combined ocean, ocean-ridge, continent and continent-arc provinces.Q^?1_R determined from pure-path average group velocities and attenuation coefficients has been regionalized successfully for 2- and 3-region combinations. The resulting pure-path Q^?1_R for continents is much lower than that for ocean basins and ocean-ridge provinces. Inversion of Q^?1_R for ocean-ridge provinces shows that the average Q_β for the upper 200 km of these regions is between 85 and 100.     

Petrochemistry and origin of pleistocene volcanic rocks from northern Taiwan

The Pleistocene volcanic rocks from northern Taiwan include the Tatun volcano group and the Chilung volcano group. Three rock types occur in this area: Tatun volcano group yield high-alumina basalt and andesites, whereas the chilung volcano group mainly consists of dacites. In addition, amphibole-rich nodules have also been found in different cruptive units of the former volcano group. Around seventy sample of various rock types have been conducted for geochemical studies, including analyses of major elements and trace elements such as Co, Cr, Cu, Li, Ni, Zn, Zr, V, Rb and Sr. Results of Al₂O₃, MnO, TiO₂ total alkali content, MgO/ΣFeO and K₂O/Na₂O ratios and AMF diagram indicate that these Pleistocene volcanic rocks belong to typical calalkaline rock series. Detailed study of the trace elements reveals that these volcanic rocks are closely correlated with rocks of continental margin type with respect to Rb, Cu, Co, Ni, V and Cr contents, and K/Rb and Ni/Co ratios. These rocks are most probably derived from the fractionation of basaltic magma controlled mainly by the crystallization of amphibole and plagioclase with magnetite playing a minor role.     

Evidence for crustal assimilation by turbulently convecting,mafic alkaline magmas: Geochemistry of mantle xenolith-bearing lavas from northern Sardinia

Alkali basalt, trachybasalt and basanite magmas, containing abundant xenoliths of upper mantle origin, were erupted during the Plio-Pleistocene (2.4-0.14 Ma) in northern Sardinia. The magmas are enriched in K, Rb, Th and Ba relative to mid-ocean ridge basalts (MORB) and most ocean island basalts (OIB), resulting in high K/Nb, Th/Nb, Ba/Nb and Rb/Nb ratios. The large number of spinel peridotite inclusions in these lavas suggests that these chemical features cannot be explained by combined assimilation and fractional crystallization within the continental crust. However, volcanic rock chemistry can be explained by the assimilation of sialic rocks by turbulently convecting, mafic magmas during their ascent to the surface. Fractionation of Ba and K from the light rare earth elements (LREE) is required to explain the positive correlation of K/La and Ba/La with ⁸⁷Sr/⁸⁶Sr_(i). Consequently, bulk assimilation of crystalline basement rocks by rising, hot basaltic magmas cannot explain the observed chemical trends, and preferential melting of a low melting quartzo-feldspathic crustal component probably occurred, leaving the REE in residual phases such as apatite, zircon, sphene and amphibole. Alternatively, large ion lithophile element (LILE) enrichment may have been related to interaction of rising mafic lavas with metasomatized lithospheric mantle or enriched asthenosphere.     

The fragment of Paleo-Tethys ophiolite from central Qiangtang, Tibet:Geochemical evidence of meta-basites in Guoganjianian

N-MORB-type metabasites are discovered in the Guoganjianian area, central Qiangtang, Tibet, which are mainly metagabbro with cumulate structure and metabasalt. The rocks are distributed nearly from west to east unconformably underlying the Wanghuling Group of upper Triassic. On the basis of geo- chemical analysis, we find that the content of SiO2 is 43.03%―53.42%, and TiO2 1%―2.67%, Al2O3 16.75%―21.52%, CaO 7.03%―11.13%, K2O 0.05%―0.38%; the REE pattern is slight depletion or flat, and the trace spider diagram is like that of N-MORB, so we consider that the metabasite was formed under the setting of mid-ocean ridge or adult back-arc basin, and it is the fragment of Paleo-Tethys ophiolite.     

Melting of the silica isotypes SiO 2, BeF 2 and GeO 2 at elevated pressures

The melting curves of the structural analogues SiO ₂, BeF ₂ and GeO ₂ have been studied at pressures ?40 kbar in a piston-cylinder apparatus. The initial slopes dT_m/dP of the β-quartz-liquid boundaries for SiO ₂ and BeF ₂ are ～35° while the slope of the rutile-liquid boundary for GeO ₂ is approximately 32°C/kbar. These large values of dT/dP reflect the unusually low entropies of fusion for these compounds in which strong structural similarities exist between the crystalline phases and the melt. Implications for the extended phase diagram of silica are discussed and it is concluded that either: (1) a maximum exists on the coesite melting curve, or (2) estimates of the melting temperature of stishovite need to be revised upwards.