Experimental peridotite–melt reaction at one atmosphere: a textural and chemical study

Sieve-textured clinopyroxene and spinel are common in mantle xenoliths and have been interpreted to be the result of partial melting, mantle metasomatism and host magma–xenolith reaction during transport. In this paper, we test the latter hypothesis with a series of reduced and oxidized experiments at 1,200 and 1,156°C at one atmosphere using a synthetic leucitite melt and discs of natural peridotite. Our results show that sieve texture development on clinopyroxene and spinel in mantle xenoliths is the result of a multistage reaction process. In the first step, orthopyroxene undergoes incongruent dissolution to produce a silica and alkali-rich melt together with olivine. As this melt migrates along grain boundaries it causes incongruent dissolution of clinopyroxene and spinel. The incongruent dissolution mechanism involves complete dissolution of the clinopyroxene or spinel followed by nucleation and growth of a secondary clinopyroxene or spinel once the reacting melt is saturated. The reaction of orthopyroxene, clinopyroxene and spinel with infiltrated host magma results in a range of melt compositions that are very similar to those interpreted to be due to very small degrees of partial melting. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Carbonate-rich melt infiltration in peridotite xenoliths from the Eurasian–North American modern plate boundary (Chersky Range,Yakutia)

A suite of mainly spinel peridotite and subordinate pyroxenite xenoliths and megacrysts were studied in detail, enabling us to characterize upper mantle conditions and processes beneath the modern North American–Eurasian continental plate boundary. The samples were collected from 37-Ma-old basanites cropping out in the Main Collision Belt of the Chersky Range, Yakutia Republic (Russian Far East). The spinel lherzolites reflect a mantle sequence, equilibrated at temperatures of 890–1,025 °C at pressures of 1.1–2 GPa, with melt extraction estimated to be around 2–6 %. The spinel harzburgites are characterized by lower P–T equilibration conditions and estimated melt extraction up to 12 %. Minor cryptic metasomatic processes are recorded in the clinopyroxene trace elements, revealing that percolating hydrous fluid-rich melts and basaltic melts affected the peridotites. One of the lherzolites preserves a unique melt droplet with primary dolomite in perfect phase contact with Na-rich aluminosilicate glass and sodalite. On the basis of the well-constrained P–T frame of the xenolith suite, as well as the rigorously documented melt extraction and metasomatic history of this upper mantle section, we discuss how a carbonated silicate melt infiltrated the lherzolite at depth and differentiated into an immiscible carbonate and silicate liquid shortly before the xenolith was transported to the surface by the host basalt. Decreasing temperatures triggered crystallization of primary dolomite from the carbonate melt fraction and sodalite as well as quenched glass from the Na-rich aluminosilicate melt fraction. Rapid entrainment and transport to the Earth’s surface prevented decarbonatization processes as well as reaction phenomena with the host lherzolite, preserving this exceptional snapshot of upper mantle carbonatization and liquid immiscibility.     

Mafic and silica-rich glasses in mantle xenoliths from Wau-en-Namus,Libya: Textural and geochemical evidence for peridotite–melt reactions

Anhydrous spinel peridotite xenoliths in Quaternary nepheline-basanite and melilite- or sodalite-bearing lavas of the Wau-en-Namus volcano in S Libya range from lherzolites to harzburgites recording melt extraction in a shallow setting (≤ 2 GPa). Primary clinopyroxenes have distinct trace element characteristics documenting LILE (large ion lithophile element) depletion or enrichment events predating the formation of glass pockets and veins in the xenoliths. These glasses are aluminous and alkali-rich, range in composition from ultrabasic to silicic (43–67 wt.% SiO₂) and may contain empty vugs and micro-phenocrysts of olivine, clinopyroxene, spinel, plagioclase, sodalite, apatite that are similar in composition to phenocrysts in the host lavas. Reactions of infiltrating melt and xenolith minerals are documented by diffuse Fe–Ca-rich rims of olivine in contact with glass, and by spongy-textured reaction domains caused by incongruent dissolution of primary pyroxenes and spinel. Some glasses have trace element characteristics similar to that of the host Ne-basanite, suggesting they were derived from the same source during entrainment and transport to the surface. Incompatible element enrichment and Sr–Nd isotopic compositions of the analyzed host lava are similar to HIMU (high μ; μ = ²³⁸Pb/²⁰⁴Pb)-type magmas, but the Pb isotopic composition is less radiogenic compared to other intra-plate Neogene magmatic rocks from N Africa.     

Melt extraction and melt refertilization in mantle peridotite of the Coast Range ophiolite: an LA–ICP–MS study

The middle Jurassic Coast Range Ophiolite (CRO) is one of the most important tectonic elements in western California, cropping out as tectonically dismembered elements that extend 700 km from south to north. The volcanic and plutonic sections are commonly interpreted to represent a supra-subduction zone (SSZ) ophiolite, but models specifying a mid-ocean ridge origin have also been proposed. These contrasting interpretations have distinctly different implications for the tectonic evolution of the western Cordillera in the Jurassic. If an SSZ origin is confirmed, we can use the underlying mantle peridotites to elucidate melt processes in the mantle wedge above the subduction zone. This study uses laser ablation–inductively coupled plasma–mass spectrometry (LA–ICP–MS) to study pyroxenes in peridotites from four mantle sections in the CRO. Trace element signatures of these pyroxenes record magmatic processes characteristic of both mid-ocean ridge and supra-subduction zone settings. Group A clinopyroxene display enriched REE concentrations [e.g., Gd (0.938–1.663 ppm), Dy (1.79–3.24 ppm), Yb (1.216–2.047 ppm), and Lu (0.168–0.290 ppm)], compared to Group B and C clinopyroxenes [e.g., Gd (0.048–0.055 ppm), Dy (0.114–0.225 ppm), Yb (0.128–0.340 ppm), and Lu (0.022–0.05 ppm)]. These patterns are also evident in orthopyroxene. The differences between these geochemical signatures could be a result of a heterogeneous upper mantle or different degrees of partial melting of the upper mantle. It will be shown that CRO peridotites were generated through fractional melting. The shapes of REE patterns are consistent with variable degrees of melting initiated within the garnet stability field. Models call for 3% dry partial melting of MORB-source asthenosphere in the garnet lherzolite field for abyssal peridotites and 15–20% further partial melting in the spinel lherzolite field, possibly by hydrous melting for SSZ peridotites. These geochemical variations and occurrence of both styles of melting regimes within close spatial and temporal association suggest that certain segments of the CRO may represent oceanic lithosphere, attached to a large-offset transform fault and that east-dipping, proto-Franciscan subduction may have been initiated along this transform.     

Melt–peridotite interaction in the shallow lithospheric mantle of the North China Craton: evidence from melt inclusions in the quartz-bearing orthopyroxene-rich websterite from Hannuoba

To better understand the origin, migration, and evolution of melts in the lithospheric mantle and their roles on the destruction of the North China Craton (NCC), we conducted a petrological and geochemical study on a quartz-bearing orthopyroxene-rich websterite xenolith from Hannuoba, the NCC, and its hosted melt and fluid inclusions. Both clinopyroxene and orthopyroxene in the xenolith contain lots of primary and secondary inclusions. High-temperature microthermometry of melt inclusions combined with Raman spectroscopy analyses of coexisting fluid inclusions shows that the entrapment temperature of the densest inclusions was ~1215°C and the pressure ~11.47 kbar, corresponding to a depth of ~38 km, i.e. within the stability of the spinel lherzolite. Intermediate pressure inclusions probably reflect progressive fluid entrapment over a range of depths during ascent, whereas the low-pressure inclusions (P < 2 kbar) may represent decrepitated primary inclusions. In situ laser-ablation ICP-MS analyses of major and trace elements on individual melt inclusions show that the compositions of these silicate melt inclusions in clinopyroxene and orthopyroxene are rich in SiO₂, Al₂O₃, and alkalis but poor in TiO₂ and strongly enriched in light rare earth elements (LREEs) and large ion lithophile elements (LILEs), with negative anomalies of high-field strength elements (HFSEs). These characteristics suggest that the silica-rich melts could be derived from the partial melting of subducted oceanic slab. Therefore, this kind of quartz-bearing orthopyroxene-rich websterite may be produced by interaction between the slab-derived melts with the mantle peridotite. This study provides direct evidence for the origin, migration, and evolution of melts in the lithospheric mantle, which may play an important role in the destruction of the NCC.     

Experiments on melt–rock reaction in the shallow mantle wedge

This experimental study simulates the interaction of hotter, deeper hydrous mantle melts with shallower, cooler depleted mantle, a process that is expected to occur in the upper part of the mantle wedge. Hydrous reaction experiments (~6 wt% H₂O in the melt) were conducted on three different ratios of a 1.6 GPa mantle melt and an overlying 1.2 GPa harzburgite from 1060 to 1260 °C. Reaction coefficients were calculated for each experiment to determine the effect of temperature and starting bulk composition on final melt compositions and crystallizing assemblages. The experiments used to construct the melt–wall rock model closely approached equilibrium and experienced <5% Fe loss or gain. Experiments that experienced higher extents of Fe loss were used to critically evaluate the practice of “correcting” for Fe loss by adding iron. At low ratios of melt/mantle (20:80 and 5:95), the crystallizing assemblages are dunites, harzburgites, and lherzolites (as a function of temperature). When the ratio of deeper melt to overlying mantle is 70:30, the crystallizing assemblage is a wehrlite. This shows that wehrlites, which are observed in ophiolites and mantle xenoliths, can be formed by large amounts of deeper melt fluxing though the mantle wedge during ascent. In all cases, orthopyroxene dissolves in the melt, and olivine crystallizes along with pyroxenes and spinel. The amount of reaction between deeper melts and overlying mantle, simulated here by the three starting compositions, imposes a strong influence on final melt compositions, particularly in terms of depletion. At the lowest melt/mantle ratios, the resulting melt is an extremely depleted Al-poor, high-Si andesite. As the fraction of melt to mantle increases, final melts resemble primitive basaltic andesites found in arcs globally. An important element ratio in mantle lherzolite composition, the Ca/Al ratio, can be significantly elevated through shallow mantle melt–wall rock reaction. Wall rock temperature is a key variable; over a span of <80 °C, reaction with deeper melt creates the entire range of mantle lithologies from a depleted dunite to a harzburgite to a refertilized lherzolite. Together, the experimental phase equilibria, melt compositions, and reaction coefficients provide a framework for understanding how melt–wall rock reaction occurs in the natural system during melt ascent in the mantle wedge.     

Early cretaceous subduction-related adakite-like rocks of the Gangdese Belt,southern Tibet: Products of slab melting and subsequent melt–peridotite interaction?

The limited geochronology and geochemistry data available for the Early Cretaceous igneous rocks of the southern Gangdese Belt, southern Tibet, has resulted in the proposal of conflicting geodynamic models for the generation of the widespread Cretaceous igneous rocks in the middle and northern parts of the belt. To explore this issue, we present SHRIMP U–Pb zircon data and geochemical and Sr–Nd–Pb–Hf isotopic data for the Mamen andesites from the southern margin of the Gangdese Belt. The Mamen andesites, emplaced at 136.5 Ma, are sodic (Na₂O/K₂O = 1.2–2.3) and have geochemical characteristics typical of adakites (i.e., high Al₂O₃, high La/Yb ratios and Sr contents, low Y and HREE contents, and positive Eu anomalies), except for high Cr, Ni, and MgO contents. The andesites have initial (⁸⁷Sr/⁸⁶Sr)_t ratios of 0.70413–0.70513, positive εNd(t) values of 3.7–5.8, and (²⁰⁶Pb/²⁰⁴Pb)_t ratios of 18.37–18.51, (²⁰⁷Pb/²⁰⁴Pb)_t ratios of 15.59–15.65, and (²⁰⁸Pb/²⁰⁴Pb)_t ratios of 38.43–38.72. In situ Hf isotopic analyses of zircons that had previously been dated by SHRIMP yielded positive initial εHf(t) values ranging from +11.0 to +15.5. A model calculation using trace element and Sr–Nd–Pb isotopic data indicates that several percent of subducted sediment is required to generate the Mamen andesites, which were derived via the partial melting of subducted Neo-Tethyan slab (MORB + sediment + fluid) and subsequently hybridized by peridotite in the mantle wedge. Our data indicate that the Neo-Tethyan oceanic crust was subducted northward beneath the Gangdese Belt during the Early Cretaceous at a high angle. Our results are inconsistent with a tectonic model that advocates the low-angle or flat-slab subduction of Neo-Tethyan oceanic crust in generating the widespread Cretaceous magmatism recorded in the Gangdese Belt.     

Multistage melt/fluid-peridotite interactions in the refertilized lithospheric mantle beneath the North China Craton: constraints from the Li–Sr–Nd isotopic disequilibrium between minerals of peridotite xenoliths

Elemental and Li–Sr–Nd isotopic data of minerals in spinel peridotites hosted by Cenozoic basalts allow us to refine the existing models for Li isotopic fractionation in mantle peridotites and constrain the melt/fluid-peridotite interaction in the lithospheric mantle beneath the North China Craton. Highly elevated Li concentrations in cpx (up to 24 ppm) relative to coexisting opx and olivine (<4 ppm) indicate that the peridotites experienced metasomatism by mafic silicate melts and/or fluids. The mineral δ⁷Li vary greatly, with olivine (+0.7 to +5.4‰) being isotopically heavier than coexisting opx (−4.4 to −25.9‰) and cpx (−3.3 to −21.4‰) in most samples. The δ⁷Li in pyroxenes are considerably lower than the normal mantle values and show negative correlation with their Li abundances, likely due to recent Li ingress attended by diffusive fractionation of Li isotopes. Two exceptional samples have olivine δ⁷Li of −3.0 and −7.9‰, indicating the existence of low δ⁷Li domains in the mantle, which could be transient and generated by meter-scale diffusion of Li during melt/fluid-peridotite interaction. The ¹⁴³Nd/¹⁴⁴Nd (0.5123–0.5139) and ⁸⁷Sr/⁸⁶Sr (0.7018–0.7062) in the pyroxenes also show a large variation, in which the cpx are apparently lower in ⁸⁷Sr/⁸⁶Sr and slightly higher in ¹⁴³Nd/¹⁴⁴Nd than coexisting opx, implying an intermineral Sr–Nd isotopic disequilibrium. This is observed more apparently in peridotites having low ⁸⁷Sr/⁸⁶Sr and high ¹⁴³Nd/¹⁴⁴Nd ratios than in those with high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd, suggesting that a relatively recent interaction existed between an ancient metasomatized lithospheric mantle and asthenospheric melt, which transformed the refractory peridotites with highly radiogenic Sr and unradiogenic Nd isotopic compositions to the fertile lherzolites with unradiogenic Sr and radiogenic Nd isotopic compositions. Therefore, we argue that the lithospheric mantle represented by the peridotites has been heterogeneously refertilized by multistage melt/fluid-peridotite interactions.     

Trace element modeling of aqueous fluid – peridotite interaction in the mantle wedge of subduction zones

Recently measured partition coefficients for Rb, Th, U, Nb, La (Ce), Pb, Sr, Sm, Zr, and Y between lherzolite assemblage minerals and H₂O-rich fluid (Ayers et al. 1997; Brenan et al. 1995a,b) are used in a two-component local equilibrium model to assess the effects of interaction between slab-derived aqueous fluids and wedge lherzolite on the trace element and isotopic composition of island arc basalts (IAB). The model includes four steps representing chemical processes, with each process represented by one equation with one adjustable parameter, in which aqueous fluid: (1) separates from eclogite in the subducted slab (Rayleigh distillation, mass fraction of fluid released F  ^fluid); (2) ascends through the mantle wedge in isolated packets, exchanging elements and isotopes with depleted lherzolite (zone refining, the rock/fluid mass ratio n); (3) mixes with depleted lherzolite (physical mixing, the mass fraction of fluid in the mixture X  ^fluid); (4) induces melting to form primitive IAB (batch melting, mass fraction of melt F ^melt). The amount of mantle lherzolite processed by the fluid in step (2) determines its isotopic and trace element signature and the relative contributions of slab and wedge to primitive IAB. Assuming an average depleted lherzolite composition and mineralogy (70% olivine, 26% orthopyroxene, 3% clinopyroxene and 1% ilmenite) and using nonlinear regression to adjust parameter values to obtain an optimal fit to the average composition of IAB (McCulloch and Gamble 1991) yields values of F  ^fluid= 0.20, n= 26, X  ^fluid= 0.17, and F  ^melt= 0.15, with r  ²= 0.995 and the average relative error in trace element concentration = 6%. The average composition of IAB can also effectively be modeled with no contribution from the slab other than H₂O (i.e., skip model step 1): n= 27, X  ^fluid= 0.21, F  ^melt= 0.17, with r  ²= 0.992. By the time the fluid reaches the IAB source, exchange with depleted wedge lherzolite reduces the ⁸⁷Sr/⁸⁶Sr ratio isotopic composition to near-mantle values and the slab contribution to <50% for all but the most incompatible elements (e.g., Pb). The IAB may retain the slab signature for elements such as B and Be that are highly incompatible and that have very low concentrations in the depleted mantle wedge. The relatively high equilibrium D  ^{mineral /   fluid} values measured by Ayers et al. (1997), Brenan et al. (1995a) and Stalder et al. (1998) suggest that large amounts of fluid (>5 wt%) must be added to lherzolite in the IAB source. Decreasing X  ^fluid below 0.05 causes model results to have unacceptably high levels of error and petrologically unreasonable values of F  ^melt. That H₂O contents of IAB are generally <6 wt% suggests that not all of the H₂O that metasomatizes the IAB source remains in the source to dissolve in the subsequently formed melt. Modeling of the compositions of specific primitive IAB from oceanic settings with low sediment input and depleted mantle wedges (Tonga, Marianas) shows a generally lower level of fluid-wedge interaction (low n), and therefore a larger slab component in primitive IAB. Received: 6 October 1997 / Accepted: 8 May 1998     

Interaction of peridotite with Ca-rich carbonatite melt at 3.1 and 6.5 GPa: Implication for merwinite formation in upper mantle,and for the metasomatic origin of sublithospheric diamonds with Ca-rich suite of inclusions

We performed an experimental study, designed to reproduce the formation of an unusual merwinite?+?olivine-bearing mantle assemblage recently described as a part of a Ca-rich suite of inclusions in sublithospheric diamonds, through the interaction of peridotite with an alkali-rich Ca-carbonatite melt, derived from deeply subducted oceanic crust. In the first set of experiments, we studied the reaction between powdered Mg-silicates, olivine and orthopyroxene, and a model Ca-carbonate melt (molar Na:K:Ca?=?1:1:2), in a homogeneous mixture, at 3.1 and 6.5 GPa. In these equilibration experiments, we observed the formation of a merwinite?+?olivine-bearing assemblage at 3.1 GPa and 1200 °C and at 6.5 GPa and 1300–1400 °C. The melts coexisting with this assemblage have a low Si and high Ca content (Ca#?=?molar 100?×?Ca/(Ca?+?Mg)?>?0.57). In the second set of experiments, we investigated reaction rims produced by interaction of the same Ca-carbonate melt (molar Na:K:Ca?=?1:1:2) with Mg-silicate, olivine and orthopyroxene, single crystals at 3.1 GPa and 1300 °C and at 6.5 GPa and 1400 °C. The interaction of the Ca-carbonate melt with olivine leads to merwinite formation through the expected reaction: 2Mg₂SiO₄ (olivine)?+?6CaCO₃ (liquid)?=?Ca₃MgSi₂O₈ (merwinite)?+?3CaMg(CO₃)₂ (liquid). Thus, our experiments confirm the idea that merwinite in the upper mantle may originate via interaction of peridotite with Ca-rich carbonatite melt, and that diamonds hosting merwinite may have a metasomatic origin. It is remarkable that the interaction of the Ca-carbonate melt with orthopyroxene crystals does not produce merwinite both at 3.1 and 6.5 GPa. This indicates that olivine grain boundaries are preferable for merwinite formation in the upper mantle.     

Heterogeneous lithospheric mantle metasomatism in the eastern North China Craton: He–Ar isotopes in peridotite xenoliths from Cenozoic basalts

The abundances and isotopic compositions of Helium and Argon have been analyzed in a suite of fresh spinel peridotite xenoliths in Cenozoic basalts from the eastern North China Craton (NCC) by step-wise heating experiments, to investigate the nature of noble gas reservoirs in the subcontinental lithospheric mantle beneath this region. The xenoliths include one harzburgite collected from Hebi in the interior of the NCC, two lherzolites from Hannuoba at the northern margin of the craton, and three lherzolites from Shanwang and Nushan on the eastern margin. ³He/⁴He ratios in most of the xenoliths are similar to those of mid-ocean ridge basalts (MORB) or slightly lower (2–10.5 Ra, where Ra is the ³He/⁴He ratio of the atmosphere), suggesting mixing of MORB-like and radiogenic components. One olivine separate from Nushan has a helium value of 25.3 Ra, probably suggesting cosmogenic ³He addition. The ⁴⁰Ar/³⁶Ar ratios vary from atmospheric value (296) to 1625, significantly lower than the MORB value. Available data of the peridotite xenoliths indicate the He and Ar isotopic systematics of the mantle reservoirs beneath the NCC can be interpreted as mixtures of at least three end-members including MORB-like, radiogenic and atmospheric components. We suggest that the MORB-like noble gases were derived from the underlying asthenosphere during mantle upwelling, whereas the radiogenic and recycled components probably were incorporated into the lithospheric mantle during circum-craton subduction of oceanic crust. Available data suggest that the MORB-like fluids are better preserved in the interior of the NCC, whereas the radiogenic ones are more prevalent at the margins. The Paleo-Asian ocean subduction system probably was responsible for the enriched and recycled noble gas signatures on the northern margin of the craton, while the Pacific subduction system could account for the observed He–Ar isotopic signatures beneath the eastern part. Therefore, integration of helium and argon isotopes reflects heterogeneous metasomatism in the lithospheric mantle and demonstrates the critical importance of lithospheric mantle modification related to both circum-craton subduction of oceanic crust and asthenospheric upwelling beneath the eastern NCC.     

A micro-scale investigation of melt production and extraction in the upper mantle based on silicate melt pockets in ultramafic xenoliths from the Bakony–Balaton Highland Volcanic Field (Western Hungary)

Mantle xenoliths in Neogene alkali basalts of the Bakony–Balaton Highland Volcanic Field (Western Hungary) frequently have melt pockets that contain silicate minerals, glass, and often carbonate globules. Textural, geochemical and thermobarometric data indicate that the melt pockets formed at relatively high pressure through breakdown of mainly amphibole as a result of temperature increases accompanied, in most cases, by the influx of external metasomatic agents. New elemental and Sr–Nd–Pb isotope data show that in several xenoliths the external agent was either a LIL-enriched aqueous fluid or a CO₂-rich fluid, whereas in other xenoliths the melt pockets were additionally enriched in LREE and sometimes HFSE, suggesting metasomatism by a silicate melt. The compositional character of the external agents might have been inherited by melting of a hydrated and probably carbonated deeper lithospheric component, which itself was metasomatized by melts with significant slab-derived components. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Be-daughter minerals in fluid and melt inclusions: implications for the enrichment of Be in granite–pegmatite systems

The study of re-homogenized melt inclusions in the same growth planes of quartz of pegmatites genetically linked to the Variscan granite of the Ehrenfriedersdorf complex, Erzgebirge, Germany, by ion microprobe analyses has determined high concentrations of Be, up to 10,000 ppm, in one type of melt inclusion, as well as moderate concentrations in the 100 ppm range in a second type of melt inclusion. Generally, the high Be concentrations are associated with the H₂O- and other volatile-rich type-B melt inclusions, and the lower Be concentration levels are connected to H₂O-poor type-A melt inclusions. Both inclusion types, representing conjugate melt pairs, are formed by a liquid–liquid immiscibility separation process. This extremely strong and very systematic scattering in Be provides insights into the origin of Be concentration and transport mechanisms in pegmatite-forming melts. In this contribution, we present more than 250 new analytical data and show with ion microprobe and fs-LA-ICPMS studies on quenched glasses, as well as with confocal Raman spectroscopy of daughter minerals in unheated melt inclusions, that the concentrations of Be may achieve such extreme levels during melt–melt immiscibility of H₂O-, B-, F-, P-, ± Li-enriched pegmatite-forming magmas. Starting from host granite with about 10 ppm Be, melt inclusions with 10,000 ppm Be correspond to enrichment by a factor of over 1,000. This strong enrichment of Be is the result of processes of fractional crystallization and further enrichment in melt patches of pegmatite bodies due to melt–melt immiscibility at fluid saturation. We also draw additional conclusions regarding the speciation of Be in pegmatite-forming melt systems from investigation of the Be-bearing daughter mineral phases in the most H₂O-rich melt inclusions. In the case of evolved volatile and H₂O-rich pegmatite systems, B, P, and carbonates are important for the enrichment and formation of stable Be complexes.     

Small volume andesite magmas and melt–mush interactions at Ruapehu, New Zealand: evidence from melt inclusions

Historical eruptions from Mt. Ruapehu (New Zealand) have been small (<0.001 km³ of juvenile magma) and have often occurred without significant warning. Developing better modelling tools requires an improved understanding of the magma storage and transport system beneath the volcano. Towards that end, we have analysed the volatile content and major element chemistry of groundmass glass and phenocryst-hosted melt inclusions in erupted samples from 1945 to 1996. We find that during this time period, magma has been stored at depths of ~2–9 km, consistent with inferences from geophysical data. Our data also show that Ruapehu magmas are relatively H₂O-poor (<2 wt%) and CO₂-rich (≤1,000 ppm) compared to typical arc andesites. Surprisingly, we find that melt inclusions are often more evolved than their transporting melt (as inferred from groundmass glass compositions). Furthermore, even eruptions that are separated by less than 2 years exhibit distinct major element chemistry, which suggests that each eruption involved magma with a unique ascent history. From these data, we infer that individual melt batches rise through, and interact with, crystal mush zones formed by antecedent magmas. From this perspective, we envision the magmatic system at Ruapehu as frequently recharged by small magma inputs that, in turn, cool and crystallise to varying degrees. Melts that are able to erupt through this network of crystal mush entrain (to a greater or lesser extent) exotic crystals. In the extreme case (such as the 1996 eruption), the resulting scoria contain melt inclusion-bearing crystals that are exotic to the transporting magma. Finally, we suggest that complex interactions between recharge and antecedent magmas are probably common, but that the small volumes and short time scales of recharge at Ruapehu provide a unique window into these processes.     

Ophiolite hosted chromitite formed by supra-subduction zone peridotite –plume interaction

Chromitite bodies hosted in peridotites typical of suboceanic mantle (s.l. ophiolitic) are found in the northern and central part of the Loma Caribe peridotite, in the Cordillera Central of the Dominican Republic. These chromitites are massive pods of small size (less than a few meters across) and veins that intrude both dunite and harzburgite. Compositionally, they are high-Cr chromitites [Cr# ​= ​Cr/(Cr ​+ ​Al) atomic ratio ​= ​0.71–0.83] singularly enriched in TiO₂ (up to 1.25 ​wt.%), Fe₂O₃ (2.77–9.16 ​wt.%) as well as some trace elements (Ga, V, Co, Mn, and Zn) and PGE (up to 4548 ​ppb in whole-rock). This geochemical signature is unknown for chromitites hosted in oceanic upper mantle but akin to those chromites crystallized from mantle plume derived melts. Noteworthy, the melt estimated to be in equilibrium with such chromite from the Loma Caribe chromitites is similar to basalts derived from different source regions of a heterogeneous Caribbean mantle plume. This mantle plume is responsible for the formation of the Caribbean Large Igneous Province (CLIP). Dolerite dykes with back-arc basin basalt (BABB) and enriched mid-ocean ridge basalt (E-MORB) affinities commonly intrude the Loma Caribe peridotite, and are interpreted as evidence of the impact that the Caribbean plume had in the off-axis magmatism of the back-arc basin, developed after the Caribbean island-arc extension in the Late Cretaceous. We propose a model in which chromitites were formed in the shallow portion of the back-arc mantle as a result of the metasomatic reaction between the supra-subduction zone (SSZ) peridotites and upwelling plume-related melts.     

Geochemistry and mineralogy of Platinum-group elements in the Ransko gabbro–peridotite massif,Bohemian Massif (Czech Republic)

The Ransko gabbro-peridotite massif in Eastern Bohemia is a strongly differentiated intrusive complex of Lower Cambrian age. The complex hosts low grade Ni-Cu ores mainly developed close to the contact of olivine-rich rocks with gabbros, in troctolites and, to a much lesser extent, in both pyroxene and olivine gabbros and plagioclase-rich peridotites. The ore zone is characterized by strong serpentinization and uralitization. The total Ni + Cu locally reaches up to 4 wt%. Anomalous concentrations of platinum-group elements (PGE's) (maximum 532 ppb Pd, 182 ppb Pt, 53 ppb Rh, 15 ppb Ru, 41 ppb Ir) were detected in samples of Cu-Ni and Ni-Cu ores (maximum 2.63 wt% Ni and 2.31 wt% Cu) from the Jezírka orebody. The main ore paragenesis includes pyrrhotite, pentlandite, chalcopyrite, cubanite, pyrite, magnetite, mackinawite, valleriite, ilmenite and sphalerite. During this work, michenerite, froodite, sperrylite, gold, native bismuth, altaite, tsumoite, hessite, an unnamed Bi-Ni telluride, cobaltite-gersdorffite and galena were newly identified. The host rocks originated through partial melting of a slightly depleted mantle source with noble metals scavenged from this primitive magma prior to the development of these rocks.     

Composition of a carbonatitic melt in equilibrium with lherzolite at 5.5–6.3 GPa and 1350°C

Generation of ultra-alkaline melts by the interaction of lherzolite with cardonatites of various genesis was simulated at the P–T parameters typical of the base of the subcratonic lithosphere. Experiments with a duration of 150 h were performed at 5.5 and 6.3 GPa and 1350°C. The concentrations of CaO and MgO in melts are buffered by the phases of peridotite, and the concentrations of alkalis and FeO depend on the composition of the starting carbonatite. Melts are characterized by a low (<7 wt %) concentration of SiO₂ and Ca# from 0.40 to 0.47. It is demonstrated that only high-Mg groups of carbonatitic inclusions in fibrous diamonds have a composition close to that of carbonatitic melts in equilibrium with lherzolite. Most likely, the formation of kimberlite-like melts relatively enriched in SiO₂ requires an additional source of heat from mantle plumes and probably H₂O fluid.