Evidence for heterogeneous enriched shergottite mantle sources in Mars from olivine-hosted melt inclusions in Larkman Nunatak 06319

Larkman Nunatak (LAR) 06319 is an olivine-phyric shergottite whose olivine crystals contain abundant crystallized melt inclusions. In this study, three types of melt inclusion were distinguished, based on their occurrence and the composition of their olivine host: Type-I inclusions occur in phenocryst cores (Fo_77-73); Type-II inclusions occur in phenocryst mantles (Fo_71-66); Type-III inclusions occur in phenocryst rims (Fo_61-51) and within groundmass olivine. The sizes of the melt inclusions decrease significantly from Type-I (∼150-250 μm diameter) to Type-II (∼100 μm diameter) to Type-III (∼25-75 μm diameter). Present bulk compositions (PBC) of the crystallized melt inclusions were calculated for each of the three melt inclusion types based on average modal abundances and analyzed compositions of constituent phases. Primary trapped liquid compositions were then reconstructed by addition of olivine and adjustment of the Fe/Mg ratio to equilibrium with the host olivine (to account for crystallization of wall olivine and the effects of Fe/Mg re-equilibration). The present bulk composition of Type-I inclusions (PBC1) plots on a tie-line that passes through olivine and the LAR 06319 whole-rock composition. The parent magma composition can be reconstructed by addition of 29 mol% olivine to PBC1, and adjustment of Fe/Mg for equilibrium with olivine of Fo₇₇ composition. The resulting parent magma composition has a predicted crystallization sequence that is consistent with that determined from petrographic observations, and differs significantly from the whole-rock only in an accumulated olivine component (∼10 wt%). This is consistent with a calculation indicating that ∼10 wt% magnesian (Fo_77-73) olivine must be subtracted from the whole-rock to yield a melt in equilibrium with Fo₇₇. Thus, two independent estimates indicate that LAR 06319 contains ∼10 wt% cumulate olivine.The rare earth element (REE) patterns of Type-I melt inclusions are similar to that of the LAR 06319 whole-rock. The REE patterns of Type-II and Type-III melt inclusions are also broadly parallel to that of the whole-rock, but at higher absolute abundances. These results are consistent with an LAR 06319 parent magma that crystallized as a closed-system, with its incompatible-element enrichment being inherited from its mantle source region. However, fractional crystallization of the reconstructed LAR 06319 parent magma cannot reproduce the major and trace element characteristics of all enriched basaltic shergottites, indicating local-to-large scale major- and trace-element variations in the mantle source of enriched shergottites. Therefore, LAR 06319 cannot be parental to the enriched basaltic shergottites.     

Peridotite Melting at 1 GPa: Reversal Experiments on Partial Melt Compositions Produced by Peridotite-Basalt Sandwich Experiments

One of the goals of igneous petrology is to use the subtle andmore obvious differences in the geochemistry of primitive basaltsto place constraints on mantle composition, melting conditionsand dynamics of mantle upwelling and melt extraction. For thisgoal to be achieved, our first-order understanding of mantlemelting must be refined by high-quality, systematic data oncorrelated melt and residual phase compositions under knownpressures and temperatures. Discrepancies in earlier data onmelt compositions from a fertile mantle composition [MORB (mid-oceanridge basalt) Pyrolite mg-number 87] and refractory lherzolite(Tinaquillo Lherzolite mg-number 90) are resolved here. Errorsin earlier data resulted from drift of W/Re thermocouples at1 GPa and access of water, lowering liquidus temperatures by30–80°C. We demonstrate the suitability of the ‘sandwich’technique for determining the compositions of multiphase-saturatedliquids in lherzolite, provided fine-grained sintered oxidemixes are used as the peridotite starting materials, and thechanges in bulk composition are considered. Compositions ofliquids in equilibrium with lherzolitic to harzburgitic residueat 1 GPa, 1300–1450°C in the two lherzolite compositionsare reported. Melt compositions are olivine + hypersthene-normative(olivine tholeiites) with the more refractory composition producinga lower melt fraction (7–8% at 1300°C) compared withthe model MORB source (18–20% at 1300°C). KEY WORDS: mantle melting; sandwich experiments; reversal experiments; anhydrous peridotite melting; thermocouple oxidation; olivine geothermometry     

橄榄石微量元素原位分析的现状及其应用

随着高精度EMPA和LA-ICP-MS分析技术的发展和矿物微量元素测试精度的提高,利用橄榄石中的微量元素示踪地幔部分熔融、地幔交代作用、岩浆早期结晶过程等地质问题成为近年来一个新兴的研究方向。一系列开拓性的研究发现也被陆续的发表,主要涉及橄榄石中Ni、Co、Al、Cr、Zn、Ti、Li、V、Sc、Mn、Ca和P等元素的示踪使用。一些卓有成效的示踪方法为:Ca、Al、Ti、Ni及Mn能够很好的用于区分橄榄石捕掳晶和斑晶;橄榄石-尖晶石地幔演化趋势线(OSMA:olivine-spinel mantle array)图解可以用于表征岩浆源区的亏损程度;玄武岩中橄榄石斑晶的Li同位素及Li含量可以很有效地指示岩浆源区是否存在地壳物质再循环及地幔交代作用;橄榄石斑晶中Ni、Ca、Mn、Cr和Al协变关系图解可以识别岩浆的辉石岩源区;利用橄榄石捕掳晶中Zr和Sc的含量差异特征可将橄榄岩中三种最主要的类型(尖晶石橄榄岩、石榴石橄榄岩以及尖晶石-石榴石橄榄岩)区分开来;一些元素的比值或组合(例如Ni/Co、Fe/Mn、V/Sc、Zr和Sc、Ca和Ti)可以指示源区交代作用、岩浆作用过程及氧化状态;基于橄榄石中Al、Cr及Ca的地质温度计可以为推算地幔热状态提供新方法;基于橄榄石分离结晶Fo-NiO演化线的原始岩浆计算模型可以较好的推算原始岩浆成分;利用橄榄石的环带及微量元素的扩散机制可以判别更多岩石成因信息,如识别交代介质、熔体类型以及地质构造背景等。基于上述最新研究的相关资料和已有成果,本文对橄榄石微量元素的地球化学示踪方法做系统性的归纳整理,并对橄榄石微量元素赋存状况、橄榄石微量元素测试方法、橄榄石微量元素的使用条件及需注意的问题等进行讨论,为读者在做相关研究时提供参考。     

Olivine-hosted melt inclusions in Pliocene–Quaternary lavas from the Qorveh–Bijar volcanic belt,western Iran: implications for source lithology and cooling history

ABSTRACT

Silicate melt inclusions (SMIs) are small droplets of magma that become trapped in minerals during crystal growth. SMIs in olivine crystals can provide critical information on the range of melt compositions and processes that occur during melt generation, evolution, transport, and eruption. The Pliocene–Quaternary volcanic rocks in the Qorveh–Bijar volcanic belt of western Iran show porphyritic and microlithic textures, with olivine and clinopyroxene being the dominant minerals. Magnesian olivines in these volcanic rocks contain primary SMIs. The composition and characteristic of olivine-hosted SMI of these rocks are investigated to constrain the source lithology for mafic volcanism. Bulk compositions of the SMIs overlap those of their host rocks and extend to higher CaO/Al₂O₃ values. The estimated entrapment pressures and temperatures of the studied SMIs are 9.1–10.3 kbar and 1220–1355°C. The calculated mafic parental melt contains 42.36 wt.% SiO₂, low total alkalis (3.22 wt.%), and high MgO (16.1 wt.%). Exploratory calculations using pMELTS show that this parental composition underwent variable degrees of fractional crystallization, as reflected by the variable compositions of the SMIs. Several lines of evidence including pyroxene xenocrysts and high FeO/MnO, FC3MS (FeO/CaO – 3*MgO/SiO2), and Zn/Fe ratios (14–21), suggest that a metasomatized pyroxenitic source contributed to the genesis of the parental melt. Amphibole in the SMIs indicates a high volatile content in the parental melt, which we conclude was generated from a metasomatized lithospheric mantle source. The pyroxenite source also contained garnet. Our geochemical results lead us to propose a new petrogenetic model. Specifically, we infer that a dense and unstable portion of the lithosphere underwent localized laminar detachment and downward flow, i.e. lithospheric drip. This drip underwent volatile-enhanced partial melting during descent through the underlying hot asthenosphere and generated the studied volcanic rocks.     

Petrological constraints on the origin of arc picrites,New Georgia Group,Solomon Islands

Subduction related picrites from the New Georgia archipelago (Solomon Islands) range in bulk MgO from 13 to 30 wt%. Two generations of olivine are identified based on CaO contents: High-CaO olivine phenocrysts from the picritic parental melt and low-CaO olivine xenocrysts incorporated from either lithospheric or asthenospheric upper mantle. There is also evidence that some of the low-CaO olivines are boninitic in origin. The bulk MgO range in the picrites is largely controlled by assimilation of low-CaO olivine xenocrysts. Oxidation states of the melt (FMQ+2.2), calculated from magnetite activities in liquidus chromites, constrain the MgO content of the parental melt to 13 wt%, assuming Fe–Mg exchange equilibrium between melt and liquidus olivine composition. The dry liquidus temperature of the parent melt based on this MgO content is 1340°C, about 80°C above the temperature obtained with the olivine–clinopyroxene Ca-exchange thermobarometer. The residence time of the low-CaO olivine xenocrysts in the magma, estimated from Ca- and Fe–Mg interdiffusion profiles, did not exceed 1 year.     

Conditions of crystallization of olivine shonkinites in the Inagli massif (Central Aldan)

The olivine shonkinites localized among dunites and alkali gabbroids in the northern part of the alkaline ultrabasic Inagli massif (northwestern part of Central Aldan) have been studied. The obtained data on the chemical and trace-element compositions of the rocks and minerals and the results of melt inclusion study showed that the olivine shonkinites crystallized from alkaline basanite melt enriched in Cl, S, CO2, and trace elements. Clinopyroxene crystallized at 1180-1200 °C from a homogeneous silicate-salt melt, which was probably separated into immiscible silicate and carbonate-salt fractions with temperature decreasing. The composition of the silicate fraction evolved from alkaline basanite to alkaline trachyte. The carbonate-salt fraction had an alkaline carbonate composition and was enriched in S and Cl. The same trend of evolution of clinopyroxene-hosted melts and the igneous rocks of the Inagli massif suggests that the alkali gabbroids, melanocratic alkali syenites, and pulaskites formed from the same magma, which had a near-alkaline basanite composition during its crystallization differentiation. The geochemical studies showed that the olivine shonkinites and glasses of homogenized melt inclusions in clinopyroxene grains have similar contents of trace elements, one or two orders of magnitude higher than those in the primitive mantle. The high contents of LILE (K, Rb, and Sr) and LREE in the olivine shoshonites and homogenized inclusions suggest the enriched mantle source, and the negative anomalies of HFSE and Ti are a specific feature of igneous rocks formed with the participation of crustal material. The slight depletion in HREE relative to LREE and the high (La/Yb)_n ratios in the rocks and inclusion glasses (10.0-11.4 and 4.7-6.2, respectively) suggest the presence of garnet in the mantle source.     

张广才岭地块早-中二叠世镁铁质侵入岩体的年代学、地球化学及岩石成因

双凤山基性侵入岩体位于松嫩-张广才岭地块南缘,其岩石组成主要为橄榄辉长岩.锆石LA-ICP-MS U-Pb定年显示该岩体形成于279±4 Ma.岩石矿物组成主要为橄榄石、单斜辉石、斜方辉石、高An值（80.1~87.9）斜长石以及以反应边形式存在的角闪石,矿物学特征指示其母岩浆为经历过充分流体交代的富水岩浆.全岩主微量元素组成揭示其源区物质组成为石榴子石二辉橄榄岩,部分熔融程度约20%,岩浆演化过程中经历了斜长石堆晶作用以及斜方辉石的结晶分异作用.全岩Sr-Nd同位素及锆石Hf同位素研究显示其（87Sr/86Sr）_i=0.705 2~0.706 1,并具有正的ε_Nd（t）值（0.9~1.3）和ε_Hf（t）值（0~10.2）,表明其来源于亏损的地幔源区,并且岩浆上升过程中没有经历明显的地壳混染.微量元素和同位素特征综合反映岩浆源区经历了古亚洲洋俯冲沉积物熔体和流体交代作用的改造,但起主导作用的是流体.其地球化学特征总体显示MORB以及弧型玄武岩过渡的特征,暗示其形成于弧后伸展环境.研究区基性侵入岩地幔源区的不均一性主要受到古亚洲洋多期次俯冲作用析出熔/流体对上覆地幔楔不同程度的改造.      

Geochemistry and oxygen isotopic composition of olivine in kimberlites from the Arkhangelsk province: Contribution of mantle metasomatism

The paper presents data on the composition of olivine macrocrysts from two Devonian kimberlite pipes in the Arkhangelsk diamond province: the Grib pipe (whose kimberlite belongs to type I) and Pionerskaya pipe (whose kimberlite is of type II, i.e., orangeite). The dominant olivine macrocrysts in kimberlites from the two pipes significantly differ in geochemical and isotopic parameters. Olivine macrocrysts in kimberlite from the Grib pipe are dominated by magnesian (Mg# = 0.92–0.93), Ti-poor (Ti < 70 ppm) olivine possessing low Ti/Na (0.05–0.23), Zr/Nb (0.28–0.80), and Zn/Cu (3–20) ratios and low Li concentrations (1.2–2.0 ppm), and the oxygen isotopic composition of this olivine δ¹⁸O = 5.64‰ is higher than that of olivine in mantle peridotites (δ¹⁸O = 5.18 ± 0.28‰). Olivine macrocrysts in kimberlite from the Pionerskaya pipe are dominated by varieties with broadly varying Mg# = 0.90–0.93, high Ti concentrations (100–300 ppm), high ratios Ti/Na (0.90–2.39), Zr/Nb (0.31–1.96), and Zn/Cu (12–56), elevated Li concentrations (1.9–3.4 ppm), and oxygen isotopic composition δ¹⁸O = 5.34‰ corresponding to that of olivine in mantle peridotites. The geochemical and isotopic traits of low-Ti olivine macrocrysts from the Grib pipe are interpreted as evidence that the olivine interacted with carbonate-rich melts/fluids. This conclusion is consistent with the geochemical parameters of model melt in equilibrium with the low-Ti olivine that are similar to those of deep carbonatite melts. Our calculations indicate that the variations in the δ¹⁸O of the olivine relative the “mantle range” (toward both higher and lower values) can be fairly significant: from 4 to 7‰ depending on the composition of the carbonate fluid. These variations were formed at interaction with carbonate fluid, whose δ¹⁸O values do not extend outside the range typical of mantle carbonates. The geochemical parameters of high-Ti olivine macrocrysts from the Grib pipe suggest that their origin was controlled by the silicate (water–silicate) component. This olivine is characterized by a zoned Ti distribution, with the configuration of this distribution between the cores of the crystals and their outer zones showing that the zoning of the cores and outer zones is independent and was produced during two episodes of reaction interaction between the olivine and melt/fluid. The younger episode (when the outer zone was formed) likely involved interaction with kimberlite melt. The transformation of the composition of the cores during the older episode may have been of metasomatic nature, as follows from the fact that the composition varies from grain to grain. The metasomatic episode most likely occurred shortly before the kimberlite melt was emplaced and was related to the partial melting of pyroxenite source material.     

A mantle or mafic crustal source for Proterozoic anorthosites?

Calculations of fractional crystallization (FC) and assimilation fractional crystallization (AFC) at 11 kb for a variety of primitive magmatic compositions and a mafic assimilant demonstrate that none of them has a bulk composition suitable to be parental to massif anorthosites. Mafic compositions thought to be parental to massif anorthosites have Mg′ values of 0.6 to 0.4 and form coherent arrays with moderately steep slopes on plots of TiO₂, K₂O, and P₂O₅ versus Mg′. The calculated liquid lines of descent (LLD) of basaltic magmas undergoing FC or AFC processes pass through the arrays of anorthosite parent magma compositions with much shallower slopes than the natural arrays, which indicates that the arrays of natural parental magmas were produced by a process other than FC/AFC. Also, by the time most crystallizing basaltic magmas with or without assimilation reach plagioclase saturation, their residual liquids have Mg′ values that are too low to be parental to anorthosites. MORB-like olivine tholeiites and high-aluminum olivine tholeiites (HAOT) from convergent plate margins do reach plagioclase saturation while sufficiently magnesian, but their Wo (Wollastonite) contents are too high such that they reach plagioclase saturation coexisting only with augite and do not reach orthopyroxene saturation (if at all) until Mg′ is too low. Calculations show it is not possible to produce a high-Al melt from typical mantle peridotites that has sufficient TiO₂ to make andesine-type anorthosite.

Calculation of partial melting for an average mafic crustal composition at 11 kbar provides a much closer match to the array of natural parental compositions in terms of minor element concentrations and proportions of mineral components. However, accounting for the entire array requires a more magnesian source composition. Such compositions exist in several crustal xenolith localities. Similar results were obtained using the bulk composition of the Stillwater Complex, which is used as a model mafic source (here the premise is that overdense crustal intrusions might sink back into the mantle). As with the terrain composition, this particular layered intrusion composition is not sufficiently magnesian, however, the fit improves when mixtures of early and late stage portions of the complex (i.e., the denser portions) were run as potential source regions.     

Volatile (Cl,F and S) and major element constraints on subduction-related mantle metasomatism along the alkaline basaltic backarc,Payenia, Argentina

We present data on volatile (S, F and Cl) and major element contents in olivine-hosted melt inclusions (MIs) from alkaline basaltic tephras along the Quaternary Payenia backarc volcanic province (~34°S–38°S) of the Andean Southern Volcanic Zone (SVZ). The composition of Cr-spinel inclusions and host olivines in Payenia are also included to constrain any variations in oxygen fugacity. The variation of potassium, fluorine and chlorine in MIs in Payenia can be modelled by partial melting (1–10%) of a variously metasomatised mantle. The high chlorine contents in MIs (up to 3200 ppm) from Northern Payenia require addition of subduction-related fluids to a mantle wedge, whereas volatile signatures in the southern Payenia are consistent with derivation from an enriched OIB source. Cl and Cl/K ratios define positive correlations with host olivine fosterite content (Fo_80-90) that cannot be explained by olivine fractionation, degassing and/or degree of mantle melting. Neither can the correlation between SiO₂ and TiO₂ in the MIs and host olivine Fo-content be explained by magmatic differentiation processes. Instead these correlations essentially require a south to north mantle source transition from a low Mg# pyroxenite (from recycled eclogite) to a high Mg# fluid metasomatised peridotite. The Cl/K and S/K ratios in Payenia MIs extend from enriched OIB-like signatures (south) to Andean SVZ arc like signatures (north). We show that the northward increase in S, Cl and S/K is coupled to a northward increase in melt oxidation states and thus in Fe³⁺/Fe^tot ratios in the magmas. The increase in oxidation state also correlates with an increase of Mn/Fe (olivine) ratios. We calculate that 25% of the apparent north–south pyroxenite–peridotite source variation in Payenia (based on olivine Mn/Fe ratios) can be explained by the south to north variation in melt oxidation states.     

Petrology of the parental melts and mantle sources of Siberian trap magmatism

Based on the investigation of olivine phenocrysts and melt and spinel inclusions in them from the picrites of the Gudchikhinsky Formation and olivine phenocrysts and the whole-rock geochemistry from the Tuklonsky and Nadezhdinsky formations of the Noril’sk region, the compositions and conditions of formation and evolution of the parental melts and mantle sources of Siberian trap magmatism were evaluated. Olivine phenocrysts from the samples studied are enriched in Ni and depleted in Mn compared with olivines equilibrated with the products of peridotite melting, which suggests a considerable role of a nonperidotitic component (olivine-free pyroxenite) in their mantle source. The onset of Siberian trap magmatism (Gudchikhinsky Formation) was related to the melting of pyroxenite produced by the interaction of ancient recycled oceanic crust with mantle peridotite. During the subsequent evolution of the magmatic system (development of the Tuklonsky and Nadezhdinsky formations), the fraction of the pyroxenite component in the source region decreased rapidly (to 40 and 60%, respectively) owing to the entrainment of peridotite material into the melting zone. The formation of magmas was significantly affected by the contamination by continental crustal material. The primitive magmas of the Gudchikhinsky Formation crystallized under near-surface conditions at temperatures of 1250–1170°C and oxygen fugacities 2.5–3.0 orders of magnitude below the Ni-NiO buffer. Simultaneously, the magmas were contaminated by continental silicic rocks and evaporites. The parental magmas of the Gudchikhinsky rocks corresponded to tholeiitic picrites with 11–14 wt % MgO. They were strongly undersaturated in sulfur, contained less than 0.25 wt % water and carbon dioxide, and were chemically similar to the Hawaiian tholeiites. They were produced by melting of a pyroxenite source at depths of 130–180 km in a mantle plume with a potential temperature of 1500–1580°C. The presence of low melting temperature pyroxenite material in the source of Siberian trap magmas promoted the formation of considerable volumes of melt under the thick continental lithosphere, which could trigger its catastrophic collapse. The contribution of pyroxenite-derived melt to the magmas of the Siberian trap province was no less than 40–50%. This component, whose solid residue was free of sulfides and olivine, played a key role in the origin of high contents of Ni, Cu, and Pt-group elements and low sulfur contents in the parental trap magmas and prevented the early dispersion of these elements at the expense of sulfide melt fractionation. The high contents of Cl in the magmas resulted in considerable HCl emission into the atmosphere and could be responsible for the mass extinction at the Paleozoic-Mesozoic boundary.     

Petrogenesis of olivine-phyric shergottite Larkman Nunatak 06319: Implications for enriched components in martian basalts

We report on the petrography and geochemistry of the newly discovered olivine-phyric shergottite Larkman Nunatak (LAR) 06319. The meteorite is porphyritic, consisting of megacrysts of olivine (?2.5 mm in length, Fo_77-52) and prismatic zoned pyroxene crystals with Wo₃En₇₁ in the cores to Wo_8-30En_23-45 at the rims. The groundmass is composed of finer grained olivine (<0.25 mm, Fo_62-46), Fe-rich augite and pigeonite, maskelynite and minor quantities of chromite, ulvöspinel, magnetite, ilmenite, phosphates, sulfides and glass. Oxygen fugacity estimates, derived from the olivine-pyroxene-spinel geo-barometer, indicate that LAR 06319 formed under more oxidizing conditions (QFM -1.7) than for depleted shergottites. The whole-rock composition of LAR 06319 is also enriched in incompatible trace elements relative to depleted shergottites, with a trace-element pattern that is nearly identical to that of olivine-phyric shergottite NWA 1068. The oxygen isotope composition of LAR 06319 (Δ¹⁷O = 0.29 ±0.03) confirms its martian origin.Olivine megacrysts in LAR 06319 are phenocrystic, with the most Mg-rich megacryst olivine being close to equilibrium with the bulk rock. A notable feature of LAR 06319 is that its olivine megacryst grains contain abundant melt inclusions hosted within the forsterite cores. These early-trapped melt inclusions have similar trace element abundances and patterns to that of the whole-rock, providing powerful evidence for closed-system magmatic behavior for LAR 06319. Calculation of the parental melt trace element composition indicates a whole-rock composition for LAR 06319 that was controlled by pigeonite and augite during the earliest stages of crystallization and by apatite in the latest stages. Crystal size distribution and spatial distribution pattern analyses of olivine indicate at least two different crystal populations. This is most simply interpreted as crystallization of megacryst olivine in magma conduits, followed by eruption and subsequent crystallization of groundmass olivine.LAR 06319 shows close affinity in mineral and whole-rock chemistry to olivine-phyric shergottite, NWA 1068 and the basaltic shergottite NWA 4468. The remarkable features of these meteorites are that they have relatively similar quantities of mafic minerals compared with olivine-phyric shergottites (e.g., Y-980459, Dho 019), but flat and elevated rare earth element patterns more consistent with the LREE-enriched basaltic shergottites (e.g., Shergotty, Los Angeles). This relationship can be interpreted as arising from partial melting of an enriched mantle source and subsequent crystal-liquid fractionation to form the enriched olivine-phyric and basaltic shergottites, or by assimilation of incompatible-element enriched martian crust. The similarity in the composition of early-trapped melt inclusions and the whole-rock for LAR 06319 indicates that any crustal assimilation must have occurred prior to crystallization of megacryst olivine, restricting such processes to the deeper portions of the crust. Thus, we favor LAR06319 forming from partial melting of an “enriched” and oxidized mantle reservoir, with fractional crystallization of the parent melt upon leaving the mantle.     

Olivine Tholeiites from Krafla, Iceland: Evidence for Variations in Melt Fraction within a Plume

Olivine tholeiites (8–10 wt. % MgO) from Krafla show significantcorrelations between major elements (notably Fe) and incompatibletrace elements. In particular, the samples with the highestFe contents are the most enriched in elements such as K, Ti,and light rare earth elements (LREE_s). The observed trends cannotbe explained by fractional crystallization of olivine, plagioclase,or clinopyrox-ene from a single primary magma, nor are theylikely to result from crustal contamination. The simplest explanationfor the compositional variations is that they result from imperfectmixing of primary melts, produced at different levels in theupwelling asthenosphere, which later underwent olivine fractionation.Nd and Sr isotopic data hint at the possibility that some mixingbetween two (plume and non-plume) mantle sources may also berequired. The average olivine tholeiite composition is comparedwith the average compositions of melts, predicted from parameterizationsof melting experiments, produced from mantle with differentpotential temperatures. The predicted compositions were correctedfor fractional crystallization before the comparison was made.The data compare well with the predicted average compositionof melt from mantle with a potential temperature of {small tilde}1580C. Differences between the observed and predicted compositions(notably higher Fe and lower Na in the Krafla basalts) are ascribedeither to errors related to the modelling or to the effect oftemperature- and velocity-structure of the mantle plume beneathIceland. The average REE composition of the olivine tholeiiteswas then inverted to obtain the variation of melt fraction withdepth. The predicted melt fraction rises from 00 at a depthof {small tilde} 140 km (consistent with a potential temperatureclose to 1580 C) to a maximum value of {small tilde} 03 atthe surface. The predicted melt thickness ({small tilde}22 kmwhen corrected for fractional crystallization) is consistentwith geophysical estimates of crustal thickness.     

Petrology, Mineralogy and Geochemistry of the Emeishan Continental Flood Basalts, SW China: Evidence for Activity of Mantle Plumes

Electronic microprobe analyses for olivine, clinopyroxene and Cr-spinel in picrites, which we have discovered recently in the Emeishan continental flood basalt province (ECFBP), show that the olivine is rich in Mg, and that Cr-spinel is rich in Cr. Based on the olivine-melt equilibrium, the primary parental melt compositions are calculated. The high-Mg olivine-hosted picrite can be regarded as parental melt. Thus, the melting temperature and pressure are estimated: T=1600℃ and P=4.5 GPa. It suggests that the picrites are connected with the activity of mantle plumes. Their major element composition is comparable to many other CFBs by their high Fe8, (CaO/Al2O3)8 and low Na8, indicating a high pressure. All rocks display a similar chondrite-normalized REE patterns, i.e., enrichment of LREE, relative depletion of HFSE and absence of negative Nb and Ta but depletion in P and K. Some incompatible element ratios, such as La/Ta, La/ Sm, (La/Nb)PM, (Th/Ta)PM, are in a limited range, show that they were derived     

Meimechites, porphyritic alkaline picrites, and melanephelinites of Siberia: Conditions of crystallization, parental magmas, and sources

The investigation of rocks, minerals, and melt inclusions showed that porphyritic alkaline picrites and meimechites crystallized from different parental magmas. At a similar ultrabasic composition, the alkaline picrite melts were enriched in K₂O relative to Na₂O, and contained up to 0.12–0.13 wt % F and less Cr, Ni, and H₂O (only 0.01–0.16 wt % H₂O, versus 0.6–1.6 wt % in the meimechite melts) compared with the meimechite magmas. The crystallization of alkaline picrite melts occurred under stable conditions at relatively low temperatures without abrupt changes: olivine and clinopyroxene crystallized at 1340–1285 and 1230–1200°C, respectively, as compared with 1600–1450 and 1230–1200°C in the meimechites. The alkaline picrite melts evolved toward melanephelinite, nephelinite, tephrite, and trachydolerite; whereas the meimechite magmas gave rise to subalkaline picritic rocks. The partitioning of vanadium between olivine and melt suggests that the meimechite magma crystallized under more oxidizing conditions compared with the alkaline picrite melts: the K_DV values for the meimechite melts (0.011–0.016) were three times lower than those for the alkaline picrite melts (0.045–0.052). The parental magmas of the alkaline picrites and meimechites were enriched in trace elements relative to mantle levels by factors of tens to hundreds. The alkaline picrite magma showed lower LILE and LREE contents compared with the meimechite magma. The magmas had also different indicator ratios of incompatible elements, including those immobile in aqueous fluids. It was concluded that the meimechite and alkaline picrite melts were derived from different mantle sources. The former were generated at lower degrees of melting of an undepleted mantle source, and the meimechite melts were produced by high-degree melting of a probably lherzolite-harzburgite source.     

鲁西中生代高镁辉石闪长岩中超镁铁质捕虏体成因:氧化态和铂族元素证据

鲁西莱芜晚中生代高镁闪长岩中含丰富的超镁铁质捕虏体,主要为纯橄岩(>80%),少量方辉橄榄岩(<5%)和橄榄辉石岩(<15%)。测定了代表性捕虏体的亲铁、亲铜元素含量,根据其矿物化学成分计算了捕虏体的氧化-还原状态。方辉橄榄岩遭受了不同程度富Si熔体的交代,全岩富含Cr、Co、Ni和IPGE,高IPGE/PPGE值,是地幔深度部分熔融的残留。纯橄岩由铬铁矿和高Mg橄榄石组成,全岩富含Cr、Co、Ni,贫IPGE,低IPGE/PPGE值,可能为一种镁铁质熔体的堆晶岩。纯橄岩中橄榄石成分表现出一定的变化范围,局部镁橄榄石（Fo）成分高达94,可能是堆晶中橄榄石与足够的铬铁矿反应的结果,原始熔体可能为玻镁安山质岩浆。方辉橄榄岩和纯橄岩都显示高f_O2值,FMQ+1.4~+2.4,与研究区早古生代相对还原的陆下岩石圈地幔(f_O2低于C-CO₂缓冲反应)形成鲜明对比。数据表明,中生代扬子大陆和华北克拉通碰撞之前,特提斯大洋板块和扬子大陆边缘相继俯冲到华北克拉通东缘之下,导致当时岩石圈地幔的f_O2陡升。     

Gabbro-norite cumulates from strongly depleted MORB melts in the Alpine–Apennine ophiolites

Hundred-meter wide cumulate bodies and decimetric dykelets of gabbro-norites are widespread within the distal ophiolitic peridotites from the Jurassic Ligure-Piemontese oceanic basin, now emplaced in the Alpine–Apennine orogenic system. These peridotites derived from the sub-continental mantle of the pre-Triassic Europe–Adria lithosphere and underwent profound modifications of their structural and compositional characteristics via melt–rock interaction during diffuse percolation by porous flow of upwelling asthenospheric melts. Gabbro-norite cumulates show the peculiar association of high forsteritic olivine, high-Mg# clinopyroxenes and orthopyroxenes and high anorthitic plagioclase with respect to mineral compositions in common ophiolitic and oceanic MORB gabbros. Abundance and early crystallization of magnesian orthopyroxene suggests that parental magmas of the gabbro-noritic cumulates were relatively silica-rich basaltic liquids. Clinopyroxenes and plagioclase have anomalously low Sr and LREE, resulting in highly fractionated C1-normalized LREE patterns in clinopyroxenes and negatively fractionated C1-normalized LREE patterns in plagioclases.Modal mineralogy and mineral major and trace element compositions indicate that these gabbro-norites crystallized from MORB-type basaltic liquids that were strongly depleted in Na, Ti, Zr, Sr and other incompatible trace elements relative to any erupted liquids of MORB-type ophiolites and modern oceanic lithosphere. Computed melt compositions in equilibrium with gabbro-norite clinopyroxenes are closely similar to depleted MORB-type single melt increments after 5–7% of fractional melting of a DM asthenospheric mantle source under spinel-facies conditions.Present knowledge on the ophiolitic peridotites of Monte Maggiore indicate that they were formed by interaction of lithospheric mantle protoliths with depleted, MORB-type single melt increments produced by the ascending asthenosphere. Their composition was progressively modified from olivine-saturated to orthopyroxene-saturated by the early reactive melt–peridotite interaction (i.e., pyroxene dissolution and olivine precipitation).Gabbro-norite cumulates marked the change from diffuse porous flow percolation to intrusion and crystallization when cooling by conducive heat loss became dominant on heating by melt percolation. Progressive upwelling and cooling of the host peridotite during rifting caused transition to more brittle conditions and to hydration and serpentinization.The Monte Maggiore peridotite body was then intruded along fractures by variably evolved, Mg–Al- to Fe–Ti-rich gabbroic dykes. Computed melt compositions in equilibrium with clinopyroxenes from less evolved gabbro dykes are closely similar to aggregated MORBs. The event of gabbro intrusion indicates that aggregated MORB-type liquids: i) migrated through and stagnated in the mantle lithosphere and ii) underwent evolution into shallow ephemeral magma chambers to form the parental magmas of the gabbroic dykes and the basaltic lava flows of the Ligurian oceanic crust.     

The origin and evolution of the parental magmas of frontal volcanoes in Kamchatka: Evidence from magmatic inclusions in olivine from Zhupanovsky volcano

The paper presents data on naturally quenched melt inclusions in olivine (Fo 69–84) from Late Pleistocene pyroclastic rocks of Zhupanovsky volcano in the frontal zone of the Eastern Volcanic Belt of Kamchatka. The composition of the melt inclusions provides insight into the latest crystallization stages (∼70% crystallization) of the parental melt (∼46.4 wt % SiO₂, ∼2.5 wt % H₂O, ∼0.3 wt % S), which proceeded at decompression and started at a depth of approximately 10 km from the surface. The crystallization temperature was estimated at 1100 ± 20°C at an oxygen fugacity of ΔFMQ = 0.9–1.7. The melts evolved due to the simultaneous crystallization of olivine, plagioclase, pyroxene, chromite, and magnetite (Ol: Pl: Cpx: (Crt-Mt) ∼ 13: 54: 24: 4) along the tholeiite evolutionary trend and became progressively enriched in FeO, SiO₂, Na₂O, and K₂O and depleted in MgO, CaO, and Al₂O₃. Melt crystallization was associated with the segregation of fluid rich in S-bearing compounds and, to a lesser extent, in H₂O and Cl. The primary melt of Zhupanovsky volcano (whose composition was estimated from data on the most primitive melt inclusions) had a composition of low-Si (∼45 wt % SiO₂) picrobasalt (∼14 wt % MgO), as is typical of parental melts in Kamchatka and other island arcs, and was different from MORB. This primary melt could be derived by ∼8% melting of mantle peridotite of composition close to the MORB source, under pressures of 1.5 ± 0.2 GPa and temperatures 20–30°C lower than the solidus temperature of “dry” peridotite (1230–1240°C). Melting was induced by the interaction of the hot peridotite with a hydrous component that was brought to the mantle from the subducted slab and was also responsible for the enrichment of the Zhupanovsky magmas in LREE, LILE, B, Cl, Th, U, and Pb. The hydrous component in the magma source of Zhupanovsky volcano was produced by the partial slab melting under water-saturated conditions at temperatures of 760–810°C and pressures of ∼3.5 GPa. As the depth of the subducted slab beneath Kamchatkan volcanoes varies from 100 to 125 km, the composition of the hydrous component drastically changes from relatively low-temperature H₂O-rich fluid to higher temperature H₂O-bearing melt. The geothermal gradient at the surface of the slab within the depth range of 100–125 km beneath Kamchatka was estimated at 4°C/km.     

Experimental data at 3 kbars pressure on parental magma to the Bushveld Complex

Experimental studies, mainly under 3 kbars pressure, have been undertaken on representative samples to determine if any of these compositions could be parental magma to the Bushveld Complex. One such composition, with 12.5% MgO, Mg/(Mg + Fe) of 0.72 and quartz-normative, crystallizes olivine, Fo₈₈, as liquidus mineral, at about 1,300° C, followed at only slightly lower temperature by orthopyroxene at 3 kbars pressure. There is a temperature drop of over 100° C before the appearance of plagioclase and finally clinopyroxene. This crystallization sequence is in excellent agreement with the observed sequence in the lower part of the Bushveld Complex.Results at higher pressures show that this composition cannot be a partial melt from mantle peridotite because olivine is replaced by orthopyroxene as the liquidus mineral at lower crustal pressures. A combination of olivine fractionation and contamination was probably involved in the early evolution of this magma.Experimental data on the other compositions show that they are not suitable as parental magma to the lowest portion of the complex. However, the data are used to construct phase diagrams within the basalt tetrahedron at 3 kbars pressure, which are of relevance to the crystallization of basic magmas in the upper crust.Research undertaken at the Grant Institute of Geology, University of Edinburgh, Scotland     

Garnet-Pyroxenite-Derived End-Member Magma Type in Kamchatka: Evidence from Composition of Olivine and Olivine-Hosted Melt Inclusions in Holocene Rocks of Kekuknaisky Volcano

Late Quaternary volcanoes of Sredinny Range (Kamchatka) attract geoscientists’ attention by their unusual geochemical features and geodynamic setting. They produced volcanic rocks that are enriched relative to N-MORB in most of incompatible trace elements (except HREE), including strong enrichment in large-ion lithophile elements, and show a negative Nb–Ta anomaly, which is typical for rocks formed in supra-subduction settings. However, modern subduction of the Pacific Plate does not reach the most part of Sredinny Range, as inferred by mapping of Wadati–Benioff zone or seismic tomography. We constrain the source of parental magmas for Sredinny Range volcanic rocks by combining major and trace element geochemical data for olivine and naturally quenched olivine-hosed melt inclusions for Holocene tephra layers of the Kekuknaisky field. Composition of the most magnesian olivine (Ni > 2000 ppm, Fe/Mn ≈ 75 at Mg# ~ 84–85 mol %) and geochemical characteristics of the most primitive melts (FC3MS = 0.61 ± 0.04 (2s)) are consistent with their derivation from a pyroxenite source, while elevated LREE/HREE ratios in lavas indicate that it contained garnet. This garnet-bearing pyroxenite likely originated from the lower crust or lithospheric mantle. Its melting could have occurred due to delamination and sinking into the hotter mantle.