The role and conditions of second-stage mantle melting in the generation of low-Ti tholeiites and boninites: the case of the Manihiki Plateau and the Troodos ophiolite

High-Mg, low-Ti volcanic rocks from the Manihiki Plateau in the Western Pacific share many geochemical characteristics with subduction-related boninites such as high-Ca boninites from the Troodos ophiolite on Cyprus, which are believed to originate by hydrous re-melting of previously depleted mantle. In this paper we compare the Manihiki rocks and Troodos boninites using a new dataset on the major and trace element composition of whole rocks and glasses from these locations, and new high-precision, electron microprobe analyses of olivine and Cr-spinel in these rocks. Our results show that both low-Ti Manihiki rocks and Troodos boninites could originate by re-melting of a previously depleted lherzolite mantle source (20–25% of total melting with 8–10% melting during the first stage), as indicated by strong depletion of magmas in more to less incompatible elements (Sm/Yb < 0.8, Zr/Y < 2, Ti/V < 12) and high-Cr-spinel compositions (Cr# > 0.5). In comparison with Troodos boninites, the low-Ti Manihiki magmas had distinctively lower H₂O contents (< 0.2 vs. > 2 wt% in boninites), ~ 100 °C higher liquidus temperatures at a given olivine Fo-number, lower fO₂ (ΔQFM < + 0.2 vs. ΔQFM > + 0.2) and originated from deeper and hotter mantle (1.4–1.7 GPa, ~ 1440 °C vs. 0.8–1.0 GPa, ~ 1300 °C for Troodos boninites). The data provide new evidence that re-melting of residual upper mantle is not only restricted to subduction zones, where it occurs under hydrous conditions, but can also take place due to interaction of previously depleted upper mantle with mantle plumes from the deep and hotter Earth interior.     

Petrogenesis of a tholeiite-boninite sequence from Ayios Mamas,Troodos ophiolite: evidence for splitting of a volcanic arc?

Lavas and intrusives from Ayios Mamas, at the western end of the Limassol Forest Complex, south of the Arakapas Fault Belt, Troodos, comprise three groups: (A) a basal sequence of pillow lavas (intruded by dikes and sills) with the phenocryst assemblage PLAG+CPX+MT±OL; (B) a middle sequence of pillows and massive flows [CPX+PLAG±OL]; and (C) an upper sequence mostly of pillows and breccia [OL+OPX+CPX+SP]. The lower group is tholeiitic, and the upper two groups boninitic. Group C whole-rock and glass Mg-numbers exceed 72 and range up to 78, with corresponding olivine compositions of Fo₉₂. They are strongly depleted in high-field strength elements, and on the basis of Cr-Y variation and major element mass balances, are interpreted to reflect partial melting of a basalt-depleted (CPX-) harzburgite source. Group A tholeiites, in contrast, are interpreted to derive from a more fertile lherzolite source. Magmaphile and compatible trace element variation is best modelled after an open magma system, involving periodic replenishment, tapping, and fractionation, although neither tholeiites nor boninites represent steady-state compositions. The boninites belong to a CaO-rich, SiO₂-poor variant, resembling those from Guam, but contrasting with those from Bonin and Cape Vogel. MORB-normalized enrichment of low-field strength elements K, Sr, Ba, and Rb in all groups indicates subduction-derived source contamination. It is proposed that the Ayios Mamas section reflects splitting of a volcanic arc, prior to back-arc spreading in an environment analogous to that of the present-day Andaman Sea.     

Potassic primary melts of vulsini (Roman Province): evidence from mineralogy and melt inclusions

The origin and the relationships between the high potassic (HKS) and potassic (KS) suites of the Roman Comagmatic Province and the nature of their primary magmas have been intensively debated over the past 35 years. We have addressed these problems by a study of mineralogy (olivine Fo_92-87, Cr-spinel and diopside) and melt inclusions in olivine phenocrysts from a scoria sample of Montefiascone (Vulsini area). This rock is considered as one of the most primitive (MgO=13.5 wt%, NiO=340 ppm; Cr=1275 ppm) in the northern part of the Roman Comagmatic Province. The compositions of both the olivine and their melt inclusions are controlled by two main processes. In the case of the olivine Fo<90.5, fractional crystallization (olivine + diopside + minor spinel) was the principal mechanism of the magma evolution. The olivine (Fo_92-90.5) and the Cr-spinel (Cr#=100. Cr/(Cr+Al)=63-73) represent a near-primary liquidus assemblage and indicate the mantle origin of their parental magmas. The compositions of melt inclusions in these olivine phenocrysts correspond to those of poorly fractionated H₂O-rich ( 1 wt%) primary melts (MgO=8.4-9.7 wt%,FeO^total=6-7.5 wt%). They evidence a wide compositional range (in wt%: SiO₂=46.5-50, K₂O=5.3-2.8, P₂O₅=0.4-0.2, S=0.26-0.12; Cl=0.05-0.03, and CaO/Al₂O₃= 0.8-1.15), with negative correlations between SiO₂ and K₂O, Al₂O₃ and CaO, as well as positive correlations between K₂O, and P₂O₅, S, Cl, with nearly constant ratios between these elements. These results are discussed in terms of segregation of various mantle-derived melts. The high and constant Mg# [100.Mg/(Mg+Fe²⁺)] 73-75 of studied melts and their variable Si, K, P, Ca, Al, S contents could be explained by the melting of a refractory lithospheric mantle source, heterogeneously enriched in phlogopite and clinopyroxene (veined mantle source).     

Potassic primary melts of Vulsini (Roman Province): evidence from mineralogy and melt inclusions

The online version of the original article can be found at     

Nd-Sr-Pb systematics and age of the Kings River ophiolite,California: implications for depleted mantle evolution

Sm-Nd whole-rock and mineral data for the Kings River ophiolite define two isochrons of 485±21 Ma and 285±45 Ma age with _Nd (483)= +10.7±0.5 and Nd (285)= +9.9±1.1, respectively. The 483 Ma isochron is defined by samples of the main igneous construct. Samples from crosscutting diabase dikes and flaser gabbro sheets within the peridotite unit yield the 285 Ma isochron. The 483 Ma data provide the first evidence of lower Paleozoic oceanic crust in the Sierran ophiolite belt. New U-Pb analyses of zircons from a plagiogranite lying on the 483 Ma Sm-Nd isochron yield upper and lower intercepts with the concordia of 430 _–60 ⁺²⁰⁰ and 183±15 Ma. Published zircon ages have underestimated the primary age of the ophiolite by 200–300 m.y. due to the effects of polymetamorphism. The 483 Ma samples have initial ⁸⁷Sr/⁸⁶Sr=0.7023–0.7030, ²⁰⁶Pb/²⁰⁴Pb=17.14–17.82, ²⁰⁷Pb/²⁰⁴Pb=15.37–15.52, ²⁰⁸Pb/²⁰⁴Pb=36.80–37.38. The 285 Ma samples have similar initial ⁸⁷Sr/⁸⁶Sr, but more radiogenic Pb. The range in Sr and Pb compositions is probably due to introduction of radiogenic Sr and Pb during multiple post-emplacement metamorphic events. The high _Nd, low ⁸⁷Sr/⁸⁶Sr, ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, ²⁰⁸Pb/²⁰⁴Pb of the least disturbed samples are clearly diagnostic of a midocean ridge origin for the 483 Ma portion of the ophiolite. Igneous activity at 285 Ma is thought to have occurred in an arc or back-arc setting, or perhaps along a leaky transform. The initial _Nd (483)=+10.7 is indistinguishable from that of the similar age Trinity Peridotite (Jacobsen et al. 1984). This value is the highest yet reported for the Mesozoic or Paleozoic depleted mantle and requires either a mantle source that was depleted 850 m.y. earlier than average or a source more highly depleted than average. Alternatively, if such values were more typical of the early Paleozoic mantle than is currently thought, then there has been little evolution of the depleted mantle over the last 500 m.y. This requires that the modern mantle has been refluxed by material with low _Nd, such as continental crust.Division Contribution # 4302 (530)     

Thin intergranular melt films and melt pockets in spinel peridotite xenoliths from the Rhön area (Germany): early stage of melt generation by grain boundary melting

Optical microscopy and transmission electron microscopy (TEM) on a porphyroclastic high temperature spinel peridotite from the Rhön area reveal fine, irregular glass layers and pockets along mineral interfaces, cracks in olivine, inside olivine crystals and in spongy rims of clinopyroxene. The chemical composition of the glass deviates significantly from the composition of the host basanite. Electron diffraction technique confirms the amorphous nature of the glass, thus classifying it as a former melt. Every grain or phase boundary shows amorphous intergranular glass layers of variable thickness and characteristic chemical composition with distinct chemical inhomogeneities. Olivine grain boundaries, as the most common type of interfaces, exhibit two different types of melt glasses: (1) Type I melt at olivine grain boundaries, which is characterized by low contents of SiO₂ (～37?wt%) and Al₂O₃ (～5?wt%) and elevated contents of MgO (～31?wt%) and FeO (～22?wt%), is supposed to have formed prior to or during the thermal overprint and the dynamic recrystallisation of the xenolith in the mantle. Melt inclusions inside olivine grains with an average composition of type I melt are suggested to be earlier melt droplets at olivine interfaces, overgrown by migrating olivine grain boundaries during recrystallization in the mantle prior to the uplift of the xenolith. (2) Type II melt, the most common type of melt in the xenolith, shows higher contents of SiO₂ (～48?wt%) and Al₂O₃ (～17?wt%) but lower contents of MgO (～20?wt%) and FeO (～11?wt%). The observation of different types of glass within a single xenolith indicates the development of different chemical melt equilibria at interfaces or triple junctions in the xenolith. The absence of geochemical trends in bivariate plots excludes a unifying process for the genesis of these glasses. Melt inclusions in the spongy rims of clinopyroxene are interpreted to be the product of a potassium-rich metasomatism. The formation of most amorphous intergranular melt layers and pockets at the mineral interfaces including type II melt at olivine grain boundaries is suggested to result from decompression melting during the uplift with the basalt magma. We suggest that these glasses were produced by grain boundary melting due to lattice mismatch and impurity segregation. The observed intergranular amorphous layers or melts represent the very beginning of mineral melting by grain boundary melting.     

Microscopic origins of macroscopic properties of silicate melts and glasses at ambient and high pressure: Implications for melt generation and dynamics

Recent development and advances in solid state NMR, together with theoretical analyses using quantum-chemical calculations and statistical mechanical modeling, have allowed us to estimate and quantify the detailed distributions of cations and anions in model silicate glasses and melts with varying pressure, temperature and composition. How these microscopic, atomic-scale distributions in the melts from NMR and simulations affect the thermodynamic and transport properties relevant to magmatic processes has been extensively explored recently. Here, based on these previous studies, we present a classification scheme to quantify the various aspects of disorder in covalent oxide glasses and melts on scales of less than 1 nm. The scheme includes contributions from both chemical and topological disorder. Chemical disorder can further be divided into [1] connectivity, which quantifies the extent of mixing among framework units (often parameterized by the degree of Al avoidance or phase separation) and the extent of polymerization (mixing between framework and nonframework cations), and [2] nonframework disorder, which denotes the distribution of network-modifying or charge-balancing cations. Topological disorder includes the distribution of bond lengths and angles. We use this framework of disorder quantification to summarize recent progress on the structures of silicate melts and glasses, mainly obtained from 2D triple quantum magic-angle spinning (3QMAS) NMR, as functions of temperature, pressure, and composition.Most glasses and melts studied show a tendency for chemical ordering in connectivity, nonframework disorder and topological disorder at ambient and high pressure. The chemical ordering in framework disorder, a manifestation of energetics in the melts and glasses, contributes to the total negative deviation of activity of oxides from ideal solution in silicate melts (reduced activity). While no definite evidence of clustering among nonframework cations was found, these cations tend to form dissimilar pairs upon mixing with other types of network modifying cations. Topological disorder in silicate glasses and melts tends to increase with increasing pressure, as suggested by increasing bond angle and length distribution, while the chemical order seems to be maintained with pressure. We calculate key macroscopic properties, including the activity coefficient of silica and viscosity, based on the quantitative estimation of the extent of disorder from solid-state NMR, in particular ¹⁷O 3QMAS NMR. Structural ordering in melts may strongly affect the composition of partial melts in equilibrium with solids, increasing the silica composition of partial melts as a result. With increasing chemical order, the configurational entropy decreases, which can be correlated to an increase in viscosity of melts.     

Parental melts of melilitolite and origin of alkaline carbonatite: evidence from crystallised melt inclusions, Gardiner complex

Perovskite and melilite crystals from melilitolites of the ultramafic alkaline Gardiner complex (East Greenland) contain crystallised melt inclusions derived from: (1) melilitite; (2) low-alkali carbonatite; (3) natrocarbonatite. The melilitite inclusion (1) homogenisation temperature of 1060 °C is similar to liquidus temperatures of experimentally investigated natural melilitites. The compositions are peralkaline, low in MgO (ca.␣5 wt%), Ni and Cr, and they are low-pressure fractionates of more magnesian larnite-normative ultramafic lamprophyre-type melts of primary mantle origin. Low-alkali carbonatite compositions (2) homogenise at 1060–1030 °C and are compositionally similar to immiscible calcite carbonatite dykes derived from the melilitolite magma. Natrocarbonatite inclusions (3) homogenise between 1030 and 900 °C and are compositionally similar to natrocarbonatite lava from Oldoinyo Lengai. Nephelinitic to phonolitic dykes which are related to the calcite carbonatite dykes, are very Zr-rich and agpaitic (molecular Na₂O + K₂O/Al₂O₃ > 1.2) and resemble nephelinites of Oldoinyo Lengai. The petrographic, geochemical and temporal relationships indicate unmixing of carbonatite compositions (ca. 10% alkalies) from evolving melilitite melt and continued fractionation of melilitite to nephelinite. It is suggested that the natrocarbonatite compositions represent degassed supercritical high temperature fluid formed in a cooling body of strongly larnite-normative nephelinite or evolved melilitite. The Gardiner complex and similar melilitolite and carbonatite-bearing ultramafic alkaline complexes are believed to represent subvolcanic complexes formed beneath volcanoes comparable to Oldoinyo Lengai and that the suggested origin of natrocarbonatite may be applied to natrocarbonatites of Oldoinyo Lengai. Received: 18 January 1996 / Accepted: 2 September 1996     

Crustal origin for coupled 'ultra-depleted' and 'plagioclase' signatures in MORB olivine-hosted melt inclusions: evidence from the Siqueiros Transform Fault,East Pacific Rise

Geochemical data from melt inclusions in olivine phenocrysts in a picritic basalt from the Siqueiros Transform Fault on the northern East Pacific Rise provide insights into the petrogenesis of mid-ocean ridge basalts (MORB). The fresh lava contains ~10% of olivine phenocrysts (Fo_89.3-91.2) and rare, small (<1 mm) plagioclase phenocrysts with subhedral to irregular shapes with a range of compositions (An_80-90, An_57-63). Melt inclusions in olivine phenocrysts are glassy, generally rounded in shape and vary in size from a few to ~200 µm. Although most of the inclusions have compositions that are generally consistent with being representative of parental melts for the pillow-rim glasses, several inclusions are clearly different. One inclusion, which contains a euhedral grain of high-Al, low-Ti spinel, has a composition unlike any melt inclusions previously described from primitive phenocrysts in MORB. It has a very high Al₂O₃ (~20 wt%), very low TiO₂ (~0.04 wt%) and Na₂O (~1 wt%) contents, and a very high CaO/Na₂O value (~14). The glass inclusion is strongly depleted in all incompatible elements (La =0.052 ppm; Yb =0.34; La/Sm(n) ~0.27), but it has large positive Sr and Eu anomalies (Sr/Sr* ~30; Eu/Eu* ~3) and a negative Zr anomaly. It also has low S (0.015 wt%) and relatively high Cl (180 ppm). We suggest that this unusual composition is a consequence of olivine trapping plagioclase in a hot, strongly plagioclase-undersaturated magma and subsequent reaction between plagioclase and the host olivine producing melt and residual spinel. Two other melt inclusions in a different olivine phenocryst have compositions that are generally intermediate between 'normal' inclusions and the aluminous inclusion, but have even higher CaO and Sr contents. They are also depleted in incompatible elements, but to a lesser degree than the aluminous inclusion, and have smaller Sr and Eu anomalies. Similar inclusions have also been described in high-Fo olivine phenocrysts from Iceland and northern Mid-Atlantic Ridge. We suggest that the compositions of these inclusions represent assimilation of gabbroic material into the hot primitive magma. The localised nature of this assimilation is consistent with it occurring within a crystal mush zone where the porosity is high as primitive magmas pass through earlier formed gabbroic 'cumulates'. In such an environment the contaminants are expected to have quite diverse compositions. Although the interaction of primitive melts with gabbroic material may not affect the compositions of erupted MORB melts on a large scale, this process may be important in some MORB suites and should be accounted for in petrogenetic models. Another important implication is that the observed variability in melt inclusion compositions in primitive MORB phenocrysts need not always to reflect processes occurring in the mantle. In particular, inferences on fractional melting processes based on geochemistry of ultra-depleted melt inclusions may not always be valid.     

Electrical conductivity of hydrous basaltic melts: implications for partial melting in the upper mantle

The Earth’s uppermost asthenosphere is generally associated with low seismic wave velocity and high electrical conductivity. The electrical conductivity anomalies observed from magnetotelluric studies have been attributed to the hydration of mantle minerals, traces of carbonatite melt, or silicate melts. We report the electrical conductivity of both H₂O-bearing (0–6 wt% H₂O) and CO₂-bearing (0.5 wt% CO₂) basaltic melts at 2 GPa and 1,473–1,923 K measured using impedance spectroscopy in a piston-cylinder apparatus. CO₂ hardly affects conductivity at such a concentration level. The effect of water on the conductivity of basaltic melt is markedly larger than inferred from previous measurements on silicate melts of different composition. The conductivity of basaltic melts with more than 6 wt% of water approaches the values for carbonatites. Our data are reproduced within a factor of 1.1 by the equation log σ = 2.172 − (860.82 − 204.46 w ^0.5)/(T − 1146.8), where σ is the electrical conductivity in S/m, T is the temperature in K, and w is the H₂O content in wt%. We show that in a mantle with 125 ppm water and for a bulk water partition coefficient of 0.006 between minerals and melt, 2 vol% of melt will account for the observed electrical conductivity in the seismic low-velocity zone. However, for plausible higher water contents, stronger water partitioning into the melt or melt segregation in tube-like structures, even less than 1 vol% of hydrous melt, may be sufficient to produce the observed conductivity. We also show that ~1 vol% of hydrous melts are likely to be stable in the low-velocity zone, if the uncertainties in mantle water contents, in water partition coefficients, and in the effect of water on the melting point of peridotite are properly considered.     

Fluid+melt intrusions in lechatelierite from the Popigai suevites: A product of dynamic interaction melts and fluids during the shock melting of the target gneiss

The paper presents data on lechatelierite form suevites of the Daldyn Formation in the Popigai astrobleme. Some of the lechatelierite samples show a complicated structure and contain block of diaplectic quartz glass and dynamic “intrusions” of glasses of types I, II, and III. The glasses of types I and II abound in fluid inclusions and display evidence of partial homogenization with lechatelierite. The glasses of type III are clearly separated from all other glasses but show evidence of dynamic interaction with them in the molten state. Fluid inclusions in the glasses of types I and II are syngenetic but have notably different densities from those of completely liquid or gaseous inclusions at 20°C. As is indicated by cryometric data, the liquid phase of the inclusions is aqueous solution of low salinity (5–8 wt % NaCl_equiv). The bulk petrochemistry of the glasses of type I characterizes them as highly silicic (96.04 wt % SiO₂ on average), with elevated K and Na concentrations (Na₂O + K₂O = 0.72 wt % on average), with 0.73 wt % Al₂O₃ (on average) and analytical totals 1.97 wt % less than 100%. The glasses of type II are also rich in SiO₂ (91.51 wt % SiO₂ on average) but contain a broader spectrum of concentrations of major oxides (totaling 5.53 wt % on average) and deficient analytical totals (by 2.96 wt % on average). The glasses of type III are completely equal to impactites produced by melting gneisses of the Popigai astrobleme. The glasses of type I are interpreted to be the intrusion products of the “early” highly mobile and H₂O-rich fluid+melt mixtures, whose protolithic material was K-Na feldspars of the target rocks. The derivation of these melts was associated with the capturing of much silica and water at a highly mobile behavior of K and Na and an inert behavior of Al. The glasses of type II were produced by the extensive mixing of silica and water at the limited involvement of apogneiss melts, and these glasses are sometimes deficient in Al. The glasses of type III are usual mixed apogneiss melts. Excess silica in the glasses of types I and II and their richness in water and deficiency in Al suggest impact anatexis and the selective separation of components during their derivation; the parental fluid-melt mixtures of these glasses were derived from such “hydrous” varieties of the target gneisses as diaphthorized and fractured rocks. The evolution and partial vitrification of lechatelierite and the glasses of types I and II proceeded under residual shock pressures, as follows from data on the dense (from ∼0.5 to 1 g/cm³) aqueous inclusions in these glasses, which suggest that the inclusions were captured in the glasses under pressures from ∼0.8 to 3.3 GPa. It follows that our lechatelierite samples have a complex multistage genesis, and their quenching facilitated the preservation of “intrusions” of various stages of shock melting, including the products of the “early” impact anatexis of the gneisses with the selective separation of components at the active participation of water.     

Chemical homogeneity of high-Cr chromitites as indicator for widespread invasion of boninitic melt in mantle peridotite of Bir Tuluha ophiolite,Northern Arabian Shield,Saudi Arabia

The Bir Tuluha ophiolite is one of the most famous chromitite-bearing occurrences in the Arabian Shield of Saudi Arabia, where chromitite bodies are widely distributed as lensoidal pods of variable sizes surrounded by dunite envelopes, and are both enclosed within the harzburgite host. The bulk-rock geochemistry of harzburgites and dunites is predominately characterized by extreme depletion in compatible trace elements that are not fluid mobile (e.g., Sr, Nb, Ta, Hf, Zr and heavy REE), but variable enrichment in the fluid-mobile elements (Rb and Ba). Harzburgites and dunites are also enriched in elements that have strong affinity for Mg and Cr such as Ni, Co and V. Chromian spinels in all the studied chromitite pods are of high-Cr variety; Cr-ratio (Cr/(Cr + Al) atomic ratio) show restricted range between 0.73 and 0.81. Chromian spinels of the dunite envelopes also show high Cr-ratio, but slightly lower than those in the chromitite pods (0.73–0.78). Chromian spinels in the harzburgite host show fairly lower Cr-ratio (0.49–0.57) than those in dunites and chromitites. Platinum-group elements (PGE) in chromitite pods generally exhibit steep negative slopes of typical ophiolitic chromitite PGE patterns; showing enrichment in IPGE (Os, Ir and Ru), over PPGE (Rh, Pt and Pd). The Bir Tuluha ophiolite is a unimodal type in terms of the presence of Ru-rich laurite, as the sole primary platinum-group minerals (PGM) in chromitite pods. These petrological features indicates that the Bir Tuluha ophiolite was initially generated from a mid-ocean ridge environment that produced the moderately refractory harzburgite, thereafter covered by a widespread homogeneous boninitic melt above supra-subduction zone setting, that produced the high-Cr chromitites and associated dunite envelopes. The Bir Tuluha ophiolite belt is mostly similar to the mantle section of the Proterozoic and Phanerozoic ophiolites, but it is a “unimodal” type in terms of high-Cr chromitites and PGE-PGM distribution.     

Water and carbon dioxide in magmatic melts and peculiarities of the melting process

The solubility of water in acid, basic and ultrabasic magmas, from experimental data at pressures up to 10 kb, increases with increasing . At pressures which apparently correspond to those of the upper mantle, maximum of solubility should be expected. Further increase of pressure decreases the concentration of water in the melt. At pressures up to 5 kb, the solubility of carbon dioxide in magmas of the same composition is considerably less than that of water. The solubility of CO₂ rises with increasing pressure at temperatures above 1000° C. The separation of a fluid phase from magmas during their movement to the earth's surface must be characterised by diminution of part of the CO₂ in the vapor along with decreasing pressure. The solubility of CO₂ at pressures of more than 10–20 kb is expected to be significant and possibly to approach that of the solubility of water. In the field of the low pressures the influence of CO₂ on the temperature of melting of silicates is significantly less than that of water. Increase of CO₂ concentration in the fluid phase with depth determines the rise of temperature minimum on the curve of rock melting. This may be connected with the appearance of processes of local melting. Approximately within the ranges of the Earth crust water separation from magmas of basic and acid composition must be attended by heat absorption and the processes of water dissolution from the environment by heat liberation.Presented at the symposium Recent Advances in the Studies of Rocks and Minerals at High Pressures and Temperatures held in Montreal, 1972. Jointly sponsored by the International Mineralogical Association and the Commission on Experimental Petrology.     

Olivine/melt transition metal partitioning, melt composition, and melt structure—Influence of Al for Si substitution in the tetrahedral network of silicate melts

The influence on olivine/melt transition metal (Mn, Co, Ni) partitioning of substitution in the tetrahedral network of silicate melt structure has been examined at ambient pressure in the 1450-1550 °C temperature range. Experiments were conducted in the systems NaAlSiO₄-Mg₂SiO₄- SiO₂ and CaAl₂Si₂O₈-Mg₂SiO₄-SiO₂ with about 1 wt% each of MnO, CoO, and NiO added. These compositions were used to evaluate how, in silicate melts, substitution and ionization potential of charge-balancing cations affect activity-composition relations in silicate melts and mineral/melt partitioning.The exchange equilibrium coefficient, , is a positive and linear function of melt Al/(Al + Si) at constant degree of melt polymerization, NBO/T. The is negatively correlated with the ionic radius, r, of the M-cation and also with the ionization potential (Z/r², Z = electrical charge) of the cation that serves to charge-balance Al³⁺ in tetrahedral coordination in the melts. The activity coefficient ratio, (γ_M/γ_Mg)^melt, is therefore similarly correlated.These melt composition relationships are governed by the distribution of Al³⁺ among coexisting Q-species in the peralkaline (depolymerized) melts coexisting with olivine. This distribution controls Q-speciation abundance, which, in turn, controls (γ_M/γ_Mg)^melt and . The relations between melt structure and olivine/melt partitioning behavior lead to the suggestion that in natural magmatic systems mineral/melt partition coefficients are more dependent on melt composition and, therefore, melt structure the more alkali-rich and the more felsic the melt. Moreover, mineral/melt partition coefficients are more sensitive to melt composition the more highly charged or the smaller the ionic radius of the cation of interest.     

Geochemical comparison of the subvolcanic appinite suite of the British Caledonides and the durbachite suite of the Central European Hercynides: evidence for associated shoshonitic and Granitic Magmatism

Summary Subvolcanic pyroxenite-hornblendite-kentallenite-diorite-granodiorite masses of the appinite suite that are spatially and temporally associated with the much more voluminous granitic plutons of the British Caledonides have major element proportions and REE patterns indicative of shoshonitic affinities. Hornblendite-monzonite-syenogabbro-pyroxene melasyenite-durbachite-biotite-rich syenite-biotite-rich granite masses of the plutonic durbachite suite of the Bohemian Massif of the Central European Hercynides, that also are spatially and temporally associated with much more voluminous granitic plutons, have geochemical characteristics that generally correspond with those of the appinite suite. Compositionally both suites resemble lamprophyres emplaced during the latter parts of the respective episodes.Both the appinite and durbachite suites show independence of K/Rb and SiO₂ with the two suites having mainly different but somewhat overlapping K/Rb ratios. Other geochemical characters, as shown by fields and trends on K vs Rb, AFM and other plots, point to the durbachite suite representing generally more evolved products of shoshonitic magma than members of the appinite suite. However, there are different geochemical characteristics, including higher Cr/Ni ratios in the durbachite suite and Co present in lower proportions in the appinite suite. These differences are the result of different histories of freezing, remelting and partial separation and remixing of fractionation products and reflect the explosive subvolcanic vs plutonic regimes of the appinitic and durbachitic suites, respectively. Support for this petrogenesis is provided by mineral compositions and comparison of compositions of mineral phases and the rocks in which they occur.

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Ein geochemischer Vergleich der subvulkanischen Appinite der Britischen Kaledoniden und der Durbachite der Mitteleuropäischen Herzyniden: Hinweise für assoziierten shoshonitischen und granitischen Magmatismus

Zusammenfassung Subvulkanische Pyroxenit-Hornblendit-Kentallenit-Diorit-Granodioritmassen der Appinit-Gruppe, die räumlich und zeitlich mit den viel umfangreicheren Granitplutonen der Britischen Kaledoniden assoziiert sind, haben Hauptelementverteilungen und SEE Gehalte, die auf Beziehungen zu Shoshoniten hinweisen. Hornblendit-Monzonit-Syenogabbro-Pyroxen-Melasyenit-Durbachit-Biotit-reiche Syenite-Biotit-reiche Granitmassen der plutonischen Durbachitabfolge des Böhmischen Massivs der Mitteleuropäischen Herzyniden, die auch räumlich und zeitlich mit viel umfangreicheren Granitplutonen assoziiert sind, haben geochemische Charakteristika, die im allgemeinen mit denen der Appinit-Gruppe übereinstimmen. Beide Gruppen sind in ihrer Zusammensetzung Lamprophyren ähnlich, die in späteren Abschnitten der magmatischen Episoden Platz genommen haben.Sowohl in den Appinit-, wie in den Durchbachit-Abfolgen sind K/Rb und SiO₂ voneinander unabhängig, beide Gruppen haben aber verschiedene, wenn auch zum Teil einander überlappende K/Rb Verhältnisse. Andere geochemische Parameter, wie K vs Rb, AFM und andere, weisen darauf hin, daß die Durbachit-Abfolge im allgemeinen weiter entwickelte Produkte shoshonitischen Magmas darstellt, als die Mitglieder der Appinit-Gruppe. Es gibt jedoch verschiedene geochemische Charakteristika, wozu auch höhere Cr/Ni Verhältnisse in den Durbachiten und niedrige CoGehalte in den Appiniten gehren. Diese Unterschiede sind das Ergebnis verschiedener Abkhlung, Aufschmelzung und teilweiser Trennung- und Wiedermischung von Fraktionierungs-Produkten und weisen auf die explosiven subvulkanischen bzw. plutonischen Regimes der beiden Gruppen hin. Diese petrogenetische Interpretation wird durch Mineralzusammensetzungen und deren Vergleich mit den Muttergesteinen unterstützt.

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With 6 Figures     

Migration and accumulation of ultra-depleted subduction-related melts in the Massif du Sud ophiolite (New Caledonia)

The Massif du Sud is a large ophiolitic complex that crops out in the southern region of New Caledonia (SW Pacific). It is dominated by harzburgite tectonite that locally shows a transitional gradation to massive dunite up section. Clinopyroxene, orthopyroxene and plagioclase progressively appear in dunite up to the transition to layered wehrlite and orthopyroxene–gabbro. The dunite–wehrlite and wehrlite–gabbro contacts are parallel and the latter defines the paleo-Moho.Highly depleted modal, mineral and bulk rock compositions indicate that harzburgites are residues after high degrees (20–30%) of partial melting mainly in the spinel-stability field. Their relative enrichment in HFSE, LREE and MREE is due to re-equilibration of melting residues with percolating melts. Dunite formed in the Moho transition zone by reaction between residual mantle harzburgite and olivine-saturated melts that led to pyroxene dissolution and olivine precipitation. Rare clinopyroxene and plagioclase crystallized in interstitial melt pores of dunite from primitive, low-TiO₂, ultra-depleted liquids with a geochemical signature transitional between those of island arc tholeiites and boninites.Ascending batches of relatively high-SiO₂, ultra-depleted melts migrated through the Moho transition zone and generated wehrlite by olivine dissolution and crystallization of clinopyroxene, orthopyroxene and plagioclase in variable amounts. These liquids were more evolved and were produced by higher degrees of melting or from a more depleted source compared with melts that locally crystallized clinopyroxene in dunite. Ultra-depleted magmas, non-cogenetic with those that formed the Moho transition zone, ascended to the lower crust and generated gabbroic cumulates with subduction-related affinity. Thus, the ultramafic and mafic rocks in the Moho transition zone and lower crust of the Massif du Sud ophiolite are not products of fractional crystallization from a single magma-type but are the result of migration and accumulation of different melts in a multi-stage evolution.The record of high partial melting in the mantle section, and migration and accumulation of ultra-depleted subduction-related melts in the Moho transition zone and lower crust support that the Massif du Sud ophiolite is a portion of forearc lithosphere generated in an extensional regime during the early phases of the subduction zone evolution. Our results show the existence of different types of ultra-depleted melt compositions arriving at the Moho transition zone and lower crust of an infant intraoceanic paleo-arc. Ultra-depleted melts may thus be a significant component of the melt budget generated in oceanic spreading forearcs prior to aggregation and mixing of a large range of melt compositions in the crust.     

Liquid immiscibility in deep-seated magmas and the generation of carbonatite melts

This paper reviews the results of investigations of melt inclusions in minerals of carbonatites and spatially associated silicate rocks genetically related to various deep-seated undersaturated silicate magmas of alkaline ultrabasic, alkaline basic, lamproitic, and kimberlitic compositions. The analysis of this direct genetic information showed that all the deep magmas are inherently enriched in volatile components, the most abundant among which are carbon dioxide, alkalis, halides, sulfur, and phosphorus. The volatiles probably initially served as agents of mantle metasomatism and promoted melting in deep magma sources. The derived magmas became enriched in carbon dioxide, alkalis, and other volatile components owing to the crystallization and fractionation of early high-magnesium minerals and gradually acquired the characteristics of carbonated silicate liquids. When critical compositional parameters were reached, the accumulated volatiles catalyzed immiscibility, the magmas became heterogeneous, and two-phase carbonate-silicate liquid immiscibility occurred at temperatures of ≥1280–1250°C. The immiscibility was accompanied by the partitioning of elements: the major portion of fluid components partitioned together with Ca into the carbonate-salt fraction (parental carbonatite melt), and the silicate melt was correspondingly depleted in these components and became more silicic. After spatial separation, the silicate and carbonate-silicate melts evolved independently during slow cooling. Differentiation and fractionation were characteristic of silicate melts. The carbonatite melts became again heterogeneous within the temperature range from 1200 to 800–600°C and separated into immiscible carbonate-salt fractions of various compositions: alkali-sulfate, alkali-phosphate, alkali-fluoride, alkali-chloride, and Fe-Mg-Ca carbonate. In large scale systems, polyphase silicate-carbonate-salt liquid immiscibility is usually manifested during the slow cooling and prolonged evolution of deeply derived melts in the Earth’s crust. It may lead to the formation of various types of intrusive carbonatites: widespread calcite-dolomite and rare alkali-sulfate, alkali-phosphate, and alkali-halide rocks. The initial alkaline carbonatite melts can retain their compositions enriched in P, S, Cl, and F only at rapid eruption followed by instantaneous quenching.     

Progressive metamorphism of the Taitao ophiolite; evidence for axial and off-axis hydrothermal alterations

We estimated metamorphic conditions for the  6 Ma Taitao ophiolite, associated with the Chile triple junction. The metamorphic grade of the ophiolite, estimated from secondary matrix minerals, changes stratigraphically downwards from the zeolite facies, through the prehnite–actinolite facies, greenschist facies and the greenschist–amphibolite transition, to the amphibolite facies. The metamorphic facies series corresponds to the low-pressure type. The metamorphic zone boundaries are subparallel to the internal lithological boundaries of the ophiolite, indicating that the metamorphism was due to axial hydrothermal alteration at a mid-ocean ridge.

Mineral assemblages and the compositions of veins systematically change from quartz-dominated, through epidote-dominated, to prehnite-dominated with increasing depth. Temperatures estimated from the vein assemblages range from  230 °C in the volcanic unit to  380 °C at the bottom of the gabbro unit, systematically  200 °C lower than estimates from the adjoining matrix minerals. The late development of veins and the systematically lower temperatures suggest that the vein-forming alteration was due to off-axis hydrothermal alteration.

Comparison between the Taitao ophiolite with its mid-ocean ridge (MOR) affinity, and other ophiolites and MOR crusts, suggests that the Taitao ophiolite has many hydrothermal alteration features similar to those of MOR crusts. This is consistent with the tectonic history that the Taitao ophiolite was formed at the South Chile ridge system near the South American continent (Anma, R., Armstrong, R., Danhara, T., Orihashi, Y. and Iwano, H., 2006. Zircon sensitive high mass-resolution ion microprobe U–Pb and fission-track ages for gabbros and sheeted dykes of the Taitao ophiolite, Southern Chile, and their tectonic implications. The Island Arc, 15(1): 130–142).