Silicate-carbonate-salt liquid immiscibility and origin of the sodalite-haüyne rocks: study of melt inclusions in olivine foidite from Vulture volcano, S. Italy

Melt inclusions in clinopyroxenes of olivine foidite bombs from Serra di Constantinopoli pyroclastic flows of the Vulture volcano (Southern Italy) were studied in detail. The rocks contain abundant zoned phenocrysts and xenocrysts of clinopyroxene, scarce grains of olivine, leucite, haüyne, glass with microlites of plagioclase and K-feldspar. The composition of clinopyroxene in xenocrysts (Cpx I), cores (Cpx II), and in rims (Cpx III) of phenocrysts differs in the content of Mg, Fe, Ti, and Al. All clinopyroxenes contain two types of primary inclusion-pure silicate and of silicate-carbonate-salt composition. This fact suggests that the phenomena of silicate-carbonate immiscibility took place prior to crystallization of clinopyroxene. Homogenization of pure silicate inclusions proceeded at 1 225 – 1 190°C. The composition of conserved melts corresponded to that of olivine foidite in Cpx I, to tephrite-phonolite in Cpx II, and phonolite-nepheline trachyte in Cpx III. The amount of water in them was no more than 0.9 wt.%. Silicate-carbonate inclusions decrepitated on heating. Salt globules contained salts of alkali-sulphate, alkali-carbonate, and Ca-carbonate composition somewhat enriched in Ba and Sr. This composition is typical of carbonatite melts when decomposed into immiscible fractions. The formation of sodalite-haüyne rocks from Vulture is related to the presence of carbonate-salt melts in magma chamber. The melts conserved in clinopyroxenes were enriched in incompatible elements, especially in Cpx III. High ratios of La, Nb, and Ta in melts on crystallization of Cpx I and Cpx II suggest the influence of a carbonatite melt as carbonatites have extremely high La/Nb and Nb/Ta and this is confirmed by the appearance of carbonatite melts in magma chamber. Some anomalies in the concentrations and relatives values of Eu and especially Ga seems typical of Italian carbonatite related melts. The mantle source for initial melts was, most likely, rather uniform, undepleted and was characterized by a low degree of melting and probable presence of garnet in restite.     

大同新生代火山岩浆的快速喷发——来自橄榄石地幔捕掳晶的证据

量化研究幔源岩浆从源区运移至喷发或者侵位的时间尺度，对理解基性岩浆作用具有重要意义。然而，对于岩浆的喷发和就位的时间尺度研究仍缺乏有效的约束，位于我国华北克拉通北部山西大同新生代火山岩群是理想的研究地区。本文以该火山群～0.2 Ma喷发的神泉寺碱性玄武岩为研究对象，重点研究其中携带的地幔橄榄石捕掳晶来约束喷发前的时间尺度。通过对其开展详细的矿物化学研究，发现地幔捕掳晶核部的Fo值高达97.7,为极富镁橄榄石，结合其极低的Ca、Mn和Ni含量特征，认为它们捕获自被交代的地幔橄榄岩。另外，地幔橄榄石捕掳晶发育明显的CaO成分环带，表明其在地壳岩浆系统内经历了复杂的岩浆演化过程。地幔橄榄石捕掳晶反应边宽度变化很大，说明它们在源区被捕获时及在运移过程中经过了多次破碎过程。橄榄石捕掳晶最边缘的Fo值为70左右，平衡计算表明它们在边部已与主岩浆(碱性玄武岩)达到平衡。Fe-Mg元素扩散计时结果显示，橄榄石地幔捕掳晶仅在岩浆中滞留了几个月的时间。对于40～70 km的岩石圈地幔厚度来说，岩浆平均上升速率最快可能超过500 m/d。     

阿尔泰南缘中泥盆统北塔山组火山岩的矿物学研究

阿尔泰山南缘中泥盆统北塔山组火山岩极为发育。本文对富辉橄玄岩和玄武岩中的单斜辉石和橄榄石斑晶进行了矿物化学分析,并结合矿物的地质温压计和岩浆结晶模拟,约束了两种岩石中矿物的形成过程,推测了原始岩浆的演化过程。提出富辉橄玄岩和玄武岩的原始岩浆属于拉斑玄武系列,富辉橄玄岩中的高压单斜辉石来源于深部（40～50 km）,其结晶早于橄榄石;玄武岩中单斜辉石大多属于岩浆房结晶产物（30～40km）,其结晶晚于橄榄石;两种岩石中橄榄石均属于岩浆房结晶产物（30～40 km）。     

Clinopyroxene phenocrysts (with green salite cores) in trachybasalts: implications for two magma chambers under the Kokchetav UHP massif, North Kazakhstan

Clinopyroxene phenocrysts in the Kokchetav trachybasalts are variable in composition and textures. Two distinctive cores are recognized: diopside cores and green salite cores. The diopside cores with Mg# of 80–90 are mantled by colorless salite rims with Mg# of 70–80. The green salite cores have especially low Mg# (<70) but high Al and Ti contents. A Mg-rich band (Mg#=82–90) usually occurs between a green salite core and its rim, and/or between a colorless salite mantle and its rim. Dissolution surfaces are observed on all textural variants. Two magma chambers are needed to explain the observed clinopyroxene phenocrysts. A deep chamber at about 120 km in the upper mantle in which diopside cores crystallized, and a shallow chamber at depths of less than 40 km in which diopside cores were resorbed and overgrown by salite rims or mantles. Magma mixing in the shallow chamber is responsible for the formation of dissolution surfaces between the diopside bands and the colorless salite mantles. The dissolution surfaces on the diopside cores formed in the shallow chamber as a result of pressure decrease. This magma evolution scenario is complicated by the occurrence of the crustal-origin green salite cores in diopsides. These green cores likely represent the relics of continental materials, which were captured in the deep chamber and partially re-melted. Our observations indicate that subducted continental materials were returned to the Earth's surface as a result of magmatism. This study therefore provides direct evidence of a link between subducted continental materials (slab) and magmatism in this orogenic belt.     

Multiple timescale constraints for high-flux magma chamber assembly prior to the Late Bronze Age eruption of Santorini (Greece)

The rhyodacitic magma discharged during the 30–80 km³ DRE (dense rock equivalent) Late Bronze Age (LBA; also called ‘Minoan’) eruption of Santorini caldera is known from previous studies to have had a complex history of polybaric ascent and storage prior to eruption. We refine the timescales of these processes by modelling Mg–Fe diffusion profiles in orthopyroxene and clinopyroxene crystals. The data are integrated with previously published information on the LBA eruption (phase equilibria studies, melt inclusion volatile barometry, Mg-in-plagioclase diffusion chronometry), as well as new plagioclase crystal size distributions and the established pre-LBA history of the volcano, to reconstruct the events that led up to the assembly and discharge of the LBA magma chamber. Orthopyroxene, clinopyroxene and plagioclase crystals in the rhyodacite have compositionally distinct rims, overgrowing relict, probably source-derived, more magnesian (or calcic) cores, and record one or more crystallization (plag???opx?>?cpx) events during the few centuries to years prior to eruption. The crystallization event(s) can be explained by the rapid transfer of rhyodacitic melt from a dioritic/gabbroic region of the subcaldera pluton (mostly in the 8–12 km depth range), followed by injection, cooling and mixing in a large melt lens at 4–6 km depth (the pre-eruptive magma chamber). Since crystals from all eruptive phases yield similar timescales, the melt transfer event(s), the last of which took place less than 2 years before the eruption, must have involved most of the magma that subsequently erupted. The data are consistent with a model in which prolonged generation, storage and segregation of silicic melts were followed by gravitational instability in the subcaldera pluton, causing the rapid interconnection and amalgamation of melt-rich domains. The melts then drained to the top of the pluton, at fluxes of up to 0.1–1 km³ year^??1, where steep vertical gradients of density and rheology probably caused them to inject laterally, forming a short-lived holding chamber prior to eruption. This interpretation is consistent with growing evidence that some large silicic magma chambers are transient features on geological timescales. A similar process preceded at least one earlier caldera-forming eruption on Santorini, suggesting that it may be a general feature of this rift-hosted magmatic system.     

A complex magmatic system beneath the Devès volcanic field,Massif Central,France: evidence from clinopyroxene megacrysts

Clinopyroxene megacrysts and mineral aggregates with clinopyroxene occur in the volcanic deposits at Mont Briançon and Marais de Limagne, which are located in the northern part of the Devès volcanic field (Massif Central, France). The clinopyroxenes can be subdivided into five groups based upon their major and trace element chemistry. Types 1a, 1b and 1c have mg# ～0.80 and are relatively Al-rich and low in Na and Fe³⁺. Subdivision into three groups is based on differing trace element signatures. Type 2 clinopyroxenes have mg# = 0.63–0.65 and higher Na and Fe³⁺ (Fe³⁺/ΣFe > 0.4) contents and may contain apatite inclusions. A type 3 megacryst is Fe-rich (mg# = ～0.52) and has the highest Na and Fe³⁺ contents, as well as containing titanite and apatite inclusions. High Fe³⁺ contents in all clinopyroxenes investigated emphasises the need to consider Fe³⁺/Fe²⁺ when assessing the petrologic origin of such megacrysts. The large range in mg# means that the clinopyroxenes could not all have crystallised from the same melt; in fact comparison with the basanitic host lavas from the two localities reveal that nearly all of the megacrysts are xenocrystic in the strict sense. The clinopyroxenes are mostly genetically related, having crystallised from related melts within the magmatic system that had undergone various degrees of differentiation. Similarities in clinopyroxene chemistry indicate that both volcanic centres are linked to the same magmatic system at depth. Assessing the depth of crystallisation reveals that types 1a and 1b formed in the lithospheric mantle, near the asthenosphere–lithosphere boundary, whereas types 1c, 2 and 3 formed in crustal magma chambers or conduits. Eruption was induced by a pulse of Mg-rich magma from the asthenosphere that entered the existing magmatic system, entraining clinopyroxene as megacrysts at several stages of ascent, before erupting at the surface. The style of eruption at Mont Briançon (cinder cone) and Marais de Limagne (maar) is different and most likely reflects local differences in near-surface hydrology. The essentially identical variety in megacrysts at the two localities suggests that eruption must have been nearly contemporaneous.     

Evidence from Antarctic mantle peridotite xenoliths for changes in mineralogy, geochemistry and geothermal gradients beneath a developing rift

Garnet and spinel peridotite xenoliths associated with the Phanerozoic Lambert-Amery Rift in eastern Antarctica contain evidence for several stages in the development of the mantle beneath the rift. Despite the fact that equilibria were only partly attained, a combination of petrography, whole-rock geochemistry, mineral chemistry and thermobarometry can be used to decipher four stages prior to entrainment of the xenoliths in the host magma during the initial stages of the breakup of Antarctica, India and Madagascar. The first chronological stage is represented by harzburgitic protoliths represented by rare occurrences of low-Ca olivines and orthopyroxenes in spinel lherzolites: these yield the lowest temperatures of 830-850 °C, and are also characterized by distinct trace element contents; lower Ti, Cr, V and Zn in olivine and orthopyroxene, and additionally lower Cu, Ni, Ga and Li in orthopyroxene. Some garnets are subcalcic, indicating that the spinel-garnet lherzolites also formed from harzburgitic protoliths. The second stage is the formation of garnet due to a pressure increase probably related to collision at 1.1 Ga. The third stage is marked by the growth of clinopyroxene, demonstrably in cpx-poor spinel lherzolites but probably in all xenolith groups: equilibrium of clinopyroxene with olivine and orthopyroxene was not attained in all samples, so that the non-judicious use of thermobarometers can produce bewildering results. The fourth stage is an enrichment episode that affected all spinel-garnet peridotites and about half of the spinel peridotites. During this stage, reaction rims were produced on the clinopyroxenes that formed during stage 3, the modal content of olivine and Mg/(Mg + Fe) in the rocks was reduced, CaO, Al₂O₃ and trace elements were enriched, and garnets were almost completely transformed to kelyphites. A later stage is documented by interstitial glasses and films around spinels related to infiltration of melt from the host magma. These post-date, and are more enriched in alkalies than, partially melted rims on clinopyroxenes, demonstrating that all the three earlier episodes were pre-entrainment events. Pressures indicated by the spinel + garnet lherzolites are restricted to 20-24 kbar at 1040-1180 °C. Early harzburgitic assemblages are interpreted to represent an earlier, cooler geotherm, whereas the kelyphite assemblages indicate temperatures 180-200 °C hotter than the main xenolith geotherm. This event also caused recrystallization of the clinopyroxene rims and is attributed to heating during rifting, but not due to the host magma itself. The preservation of evidence for three progressively hotter geotherms can be related to the upward movement of isotherms during the development of the sub-rift mantle.     

An Experimental Melting—crystallization Study on Basalt at High Pressures

A series of melting-crystallization experiments on alkali basalt samples from Minqing, Fujian Province was carried out in dry and waterbearing systems at high pressures. A high-pressure melting curve was obtained. The results indicate that clinopyroxene crystallized from basalt melt at 13.5–23.7 kbar. spinel at 23.7–28.6 kbar and garnet at > 28.6 kbar. With increasing pressure, the CaSiO₃ contents of clinopyroxenes increase; and the FeSiO₃ decreases, but the chemical composition of garnet does not show any significant difference. The minerals are larger and euhedral in the water-bearing system. Therefore, we consider that natural megacrysts of the basalt can crystallize from the water-bearing basalt magma at high pressure. So the megacrysts may be derived from the upper mantle as a result of magmatic crystallization-fractionation under high pressure. This project was financially supported by the National Natural Science Foundation of China.     

Tectonic implications of garnet-bearing mantle xenoliths exhumed by Quaternary magmatism in the Hangay dome, central Mongolia

Garnet-bearing mantle xenoliths have been recovered from Quaternary alkali basalts, both within and peripheral to the Hangay dome of central Mongolia. Microfabric analysis and thermobaromery, combining empirical thermobarometers and the self-consistent dataset of THERMOCALC, indicate that garnet websterites from the Shavaryn-Tsaram volcanic centre at the dome core were formed in the spinel-lherzolite upper mantle at pressures of 17–18 kbars and temperatures of 1,070–1,090°C, whereas garnet lherzolites were derived from greater depths (18–20 kbars). Garnet lherzolites from the Baga Togo Uul vents near the dome edge were formed at 18–22 kbars under significantly cooler conditions (960–1,000°C). These xenoliths reveal reaction coronas of (1) orthopyroxene, clinopyroxene, plagioclase and spinel mantling garnets; (2) spongy rims of olivine replacing orthopyroxene and (3) low-Na, low-Al clinopyroxene replacing primary clinopyroxene. Trace-element abundances indicate that clinopyroxene from these coronas is in chemical equilibrium with the host magma. The thermobarometric and textural data suggest that lherzolite xenoliths from both sites were derived from depths of 60–70 km and entrained in magma at 1,200–1,300°C. The average rate of ascent, as determined by olivine zoning, lies in the range 0.2–0.3 m s⁻¹. The contrast in thermal profiles of the upper mantle between the two sites is consistent with a mantle plume beneath the Hangay dome with elevated thermal conditions beneath the core of the dome being comparable to estimates of the Pleistocene geotherm beneath the Baikal rift.     

Lithium elemental and isotopic variations in rock-melt interaction

Despite the occurrence of highly variable lithium (Li) elemental distribution and isotopic fractionation in mantle mineral, the mechanism of Li heterogeneity and fractionation remains a controversial issue. We measured Li contents and isotopic compositions of olivine and clinopyroxene xenocrysts and phenocrysts from kamafugite host lavas, as well as minerals in melt pockets occurring as metasomatic products in peridotite xenoliths from the Western Qinling, central China. The olivine xenocrysts in the kamafugites show compositional zonation. The cores have high Mg# (100 × Mg/(Mg+Fe); 91.0–92.2) and Li abundances (5.63–21.7 ppm), low CaO contents (≤0.12 wt%) and low δ⁷Li values (−39.6 to −6.76‰), which overlap with the compositional ranges of the olivines in the melt pockets as well as those in peridotite xenoliths. The rims of the olivine xenocrysts display relatively low Mg# (85.9–88.2), high CaO contents (0.19–0.38 wt%) and high δ⁷Li values (18.3–26.9‰), which are comparable to the olivine phenocrysts (Mg#: 86.4–87.1; CaO: 0.20–0.28 wt%; Li: 12.4–36.8 ppm; δ⁷Li: 18.1–26.0‰) and the silicate-melt metasomatized olivines. The clinopyroxene phenocrysts and clinopyroxenes in the melt pockets have no distinct characteristics with respect to the Li abundances and δ⁷Li values, but show higher and lower CaO contents, respectively, than the clinopyroxenes from silicate and carbonatite metasomatized samples. These features indicate that Li concentration and isotopic signatures of the cores of the xenocrysts recorded carbonatite melt-peridotite reaction (carbonatite metasomatism) at mantle depth, and the variations in the rims probably resulted from xenocryst–host magma interaction during ascent. Our results reveal that the interaction with carbonatite and silicate melts gave rise to an increase in Li abundance in minerals of peridotite xenoliths at mantle depth or during transportation. In terms of δ⁷Li, the carbonatite and silicate melts produced remarkably contrasting δ⁷Li variations in olivine. Based on the systematic variations of Li abundances and Li isotopes in olivines, we suggest that the δ⁷Li value of olivine is a more important indicator than that of clinopyroxene in discriminating carbonatite and silicate melt interaction agents with peridotites.     

Mineral chemistry of submarine lavas from Hilo Ridge, Hawaii: implications for magmatic processes within Hawaiian rift zones

The crustal history of volcanic rocks can be inferred from the mineralogy and compositions of their phenocrysts which record episodes of magma mixing as well as the pressures and temperatures when magmas cooled. Submarine lavas erupted on the Hilo Ridge, a rift zone directly east of Mauna Kea volcano, contain olivine, plagioclase, augite ±orthopyroxene phenocrysts. The compositions of these phenocryst phases provide constraints on the magmatic processes beneath Hawaiian rift zones. In these samples, olivine phenocrysts are normally zoned with homogeneous cores ranging from ∼ Fo₈₁ to Fo₉₁. In contrast, plagioclase, augite and orthopyroxene phenocrysts display more than one episode of reverse zoning. Within each sample, plagioclase, augite and orthopyroxene phenocrysts have similar zoning profiles. However, there are significant differences between samples. In three samples these phases exhibit large compositional contrasts, e.g., Mg# [100 × Mg/(Mg+Fe⁺²)] of augite varies from 71 in cores to 82 in rims. Some submarine lavas from the Puna Ridge (Kilauea volcano) contain phenocrysts with similar reverse zonation. The compositional variations of these phenocrysts can be explained by mixing of a multiphase (plagioclase, augite and orthopyroxene) saturated, evolved magma with more mafic magma saturated only with olivine. The differences in the compositional ranges of plagioclase, augite and orthopyroxene crystals between samples indicate that these samples were derived from isolated magma chambers which had undergone distinct fractionation and mixing histories. The samples containing plagioclase and pyroxene with small compositional variations reflect magmas that were buffered near the olivine + melt ⇒Low-Ca pyroxene + augite + plagioclase reaction point by frequent intrusions of mafic olivine-bearing magmas. Samples containing plagioclase and pyroxene phenocrysts with large compositional ranges reflect magmas that evolved beyond this reaction point when there was no replenishment with olivine-saturated magma. Two of these samples contain augite cores with Mg# of ∼71, corresponding to Mg# of 36–40 in equilibrium melts, and augite in another sample has Mg# of 63–65 which is in equilibrium with a very evolved melt with a Mg# of ∼30. Such highly evolved magmas also exist beneath the Puna Ridge of Kilauea volcano. They are rarely erupted during the shield building stage, but may commonly form in ephemeral magma pockets in the rift zones. The compositions of clinopyroxene phenocryst rims and associated glass rinds indicate that most of the samples were last equilibrated at 2–3 kbar and 1130–1160 °C. However, in one sample, augite and glass rind compositions reflect crystallization at higher pressures (4–5 kbar). This sample provides evidence for magma mixing at relatively high pressures and perhaps transport of magma from the summit conduits to the rift zone along the oceanic crust-mantle boundary. Received: 8 July 1998 / Accepted: 2 January 1999     

An experimental study of a minette from the Milk River area, southern Alberta, Canada

Buhlmann et al. (Can J Earth Sci 37: 1629–1650, 2000) studied the minettes and xenoliths from the Milk River area of southern Alberta, Canada. Based on previous work, they hypothesized that the minettes were derived from a source containing phlogopite?+?clinopyroxene?±?olivine, at pressures ≥1.7?GPa. To test this hypothesis, liquidus experiments were performed on a primitive minette between 1.33 and 2.21?GPa and between 1,300 and 1,400?°C to constrain the mineralogy of its source region. We found a multiple saturation point along the liquidus at 1.77 GPa and 1,350?°C, where the liquid coexists with orthopyroxene and olivine. Neither phlogopite nor clinopyroxene were found to be liquidus phases, which is inconsistent with Buhlmann et al.’s hypothesis. We suggest that our minette is not primary, but had re-equilibrated with harzburgitic mantle subsequent to formation. In such a scenario, partial melting of a veined source containing mica and clinopyroxene occurred at or near the base of the Wyoming craton (~200?km). Minimal heating or the introduction of hydrous fluids into the source would be required to induce partial melting. Rapid ascent rates, coupled with slow cooling rates, of the “primary minette magma” would preserve the high temperature observed in our experiments. At ~58?km, our “primary minette magma” likely stalled and re-equilibrated with the harzburgite surroundings.     

Deep Fractionation of Clinopyroxene in the East Pacific Rise 13°N: Evidence from High MgO MORB and Melt Inclusions

Mid-ocean ridge basalts (MORBs) from East Pacific Rise (EPR) 13°N are analysed for major and trace elements, both of which show a continuous evolving trend. Positive MgO–Al2O3 and negative MgO–Sc relationships manifest the cotectic crystallization of plagioclase and olivine, which exist with the presence of plagioclase and olivine phenocrysts and the absence of clinopyroxene phenocrysts. However, the fractionation of clinopyroxene is proven by the positive correlation of MgO and CaO. Thus, MORB samples are believed to show a “clinopyroxene paradox”. The highest magnesium-bearing MORB sample E13-3B (MgO=9.52%) is modelled for isobaric crystallization with COMAGMAT at different pressures. Observed CaO/Al2O3 ratios can be derived from E13-3B only by fractional crystallization at pressure >4 ±1 kbar, which necessitates clinopyroxene crystallization and is not consistent with cotectic crystallization of olivine plus plagioclase in the magma chamber (at pressure ~1 kbar). The initial compositions of the melt inclusions, which could represent potential parental magmas, are reconstructed by correcting for post-entrapment crystallization (PEC). The simulated crystallization of initial melt inclusions also produce observed CaO/Al2O3 ratios only at >4±1 kbar, in which clinopyroxene takes part in crystallization. It is suggested that MORB magmas have experienced clinopyroxene fractionation in the lower crust, in and below the Moho transition zone. The MORB magmas have experienced transition from clinopyroxene+plagioclase+olivine crystallization at >4±1 kbar to mainly olivine+plagioclase crystallization at <1 kbar, which contributes to the explanation of the “clinopyroxene paradox”.     

Successive episodes of reactive liquid flow through a layered intrusion (Unit 9, Rum Eastern Layered Intrusion,Scotland)

We present a detailed microstructural and geochemical study of reactive liquid flow in Unit 9 of the Rum Eastern Layered Intrusion, Scotland. Unit 9 comprises an underlying lens-like body of peridotite overlain by a sequence of troctolite and gabbro (termed allivalite), with some local and minor anorthosite. The troctolite is separated from the overlying gabbro by a distinct, sub-horizontal, undulose horizon (the ‘major wavy horizon’). Higher in the stratigraphy is another, similar, horizon (the ‘minor wavy horizon’) that separates relatively clinopyroxene-poor gabbro from an overlying gabbro. To the north of the peridotite lens, both troctolite and gabbro grade into poikilitic gabbro. Clinopyroxene habit in the allivalite varies from thin rims around olivine in troctolite to equigranular crystals in gabbro and to oikocrysts in poikilitic gabbro. The poikilitic gabbros contain multiple generations of clinopyroxene, with Cr-rich (~1.1 wt% Cr₂O₃) anhedral cores with moderate REE concentrations (core1) overgrown by an anhedral REE-depleted second generation with moderate Cr (~0.7 wt% Cr₂O₃) (core2). These composite cores are rimmed by Cr-poor (~0.2 wt% Cr₂O₃) and REE-poor to -moderate clinopyroxene. We interpret these microstructures as a consequence of two separate episodes of partial melting triggered by the intrusion of hot olivine-phyric picrite to form the discontinuous lenses that comprise the Unit 9 peridotite. Loss of clinopyroxene-saturated partial melt from the lower part of the allivalite immediately following the early stages of sill intrusion resulted in the formation of clinopyroxene-poor gabbro. The spatial extent of clinopyroxene loss is marked by the minor wavy horizon. A second partial melting event stripped out almost all clinopyroxene from the lowest allivalite to form a troctolite, with the major wavy horizon marking the extent of melting during this episode. The poikilitic gabbro formed from clinopyroxene-saturated melt moving upwards and laterally through the remobilized cumulate pile and precipitating clinopyroxene en route. This process, called reactive liquid flow, is potentially important in open magma chambers.     

Melt inclusion constraints on petrogenesis of the 2014–2015 Holuhraun eruption,Iceland

The 2014–2015 Holuhraun eruption, on the Bárðarbunga volcanic system in central Iceland, was one of the best-monitored basaltic fissure eruptions that has ever occurred, and presents a unique opportunity to link petrological and geochemical data with geophysical observations during a major rifting episode. We present major and trace element analyses of melt inclusions and matrix glasses from a suite of ten samples collected over the course of the Holuhraun eruption. The diversity of trace element ratios such as La/Yb in Holuhraun melt inclusions reveals that the magma evolved via concurrent mixing and crystallization of diverse primary melts in the mid-crust. Using olivine–plagioclase–augite–melt (OPAM) barometry, we calculate that the Holuhraun carrier melt equilibrated at 2.1?±?0.7 kbar (7.5?±?2.5 km), which is in agreement with the depths of earthquakes (6?±?1 km) between Bárðarbunga central volcano and the eruption site in the days preceding eruption onset. Using the same approach, melt inclusions equilibrated at pressures between 0.5 and 8.0 kbar, with the most probable pressure being 3.2 kbar. Diffusion chronometry reveals minimum residence timescales of 1–12 days for melt inclusion-bearing macrocrysts in the Holuhraun carrier melt. By combining timescales of diffusive dehydration of melt inclusions with the calculated pressure of H₂O saturation for the Holuhraun magma, we calculate indicative magma ascent rates of 0.12–0.29 m s^?1. Our petrological and geochemical data are consistent with lateral magma transport from Bárðarbunga volcano to the eruption site in a shallow- to mid-crustal dyke, as has been suggested on the basis of seismic and geodetic datasets. This result is a significant step forward in reconciling petrological and geophysical interpretations of magma transport during volcano-tectonic episodes, and provides a critical framework for the interpretation of premonitory seismic and geodetic data in volcanically active regions.     

Origin of zircon in jadeitite from the Nishisonogi metamorphic rocks,Kyushu, Japan

On the basis of internal structures, laser ablation U–Pb ages and trace element compositions, the origin of zircon in jadeitite in the Nishisonogi metamorphic rocks was examined. The zircon comprises euhedral zoned cores overgrown by euhedral rims. The cores contain inclusions of muscovite, quartz, albite and possibly K‐feldspar, yield ²³⁸U–²⁰⁶Pb ages of 126 ± 6 Ma (±2 SD, n = 45, MSWD = 1.0), and have Th/U ratios of 0.48–1.64. The rims contain inclusions of jadeite, yield ²³⁸U–²⁰⁶Pb ages of 84 ± 6 Ma (±2 SD, n = 14, MSWD = 1.1), and have Th/U ratios of <0.06. The cores are richer in Y, Th, Ti and rare earth elements (REEs), but the rims are richer in Hf and U. Chondrite‐normalized REE patterns of the cores indicate higher Sm_N/La_N ratios, lower Yb_N/Gd_N ratios and larger positive Ce anomalies compared with those of the rims. Thus, the cores and rims have different ²³⁸U–²⁰⁶Pb ages and trace element compositions, suggesting two stages of zircon growth. Although the ²³⁸U–²⁰⁶Pb ages of the rims are consistent with the reported ⁴⁰Ar/³⁹Ar spot‐fusion ages of matrix muscovite in the jadeitite, the ²³⁸U–²⁰⁶Pb ages of the cores are older. The mineral inclusions and high Th/U ratios in the cores are best explained by crystallization from felsic magma. Therefore, the cores are considered relicts from igneous precursor rocks. The rims surrounding the inherited cores possibly precipitated from aqueous fluids during jadeitite formation. The elevated U concentrations in the rims suggest that infiltration of external fluids was responsible for the precipitation. This study provides an example of jadeitite formation by metasomatic replacement of a protolith.     

Chemical zoning of Ca-amphiboles in amphibolites,from the Hamedan area,West Iran

Amphibolite layers of the Hamedan area (Sanandaj-Sirjan zone, west Iran) contain amphibole crystals with strong optical zoning. These amphibolites occur as interlayers in middle Jurassic, Buchan-type andalusite-garnet-staurolite and sillimanite-garnet-andalusite schist of the area that were intruded by late Jurassic magmatic bodies of the Alvand plutonic complex. Electron microprobe analyses results show that the zoned amphiboles have ferrohornblende cores that change to ferroedenite toward the rims. The core-to rim increase of Al, Fe, Na, and K and decrease of Si and Mg along with edenitic substitution in amphiboles is consistent with increase in metamorphic grade. Thermobarometry calculations based on amphibole composition and hornblende-plagioclase thermometry provided 492 to 508 ^o C and 4.3 to 4.9 kbar for the inner cores, 495 to 514 ^o C and 4.5 to 5.1 kbar for the outer cores, 538 to 564 ^o C and 5.3 to 5.8 kbar for the inner rims and 552 to 573 ^o C and 5.5 to 5.9 kbar for the outer rims, respectively. These results point to a nearly isobaric prograde P-T path for the Hamedan area amphibolites, compatible with a metamorphic evolution dominated by the thermal perturbation associated with the late Jurassic magmatism of the northern Sanandaj-Sirjan zone.     

Insights into the petrogenesis of the West Kimberley lamproites from trace elements in olivine

The Miocene lamproites of the West Kimberley region, Western Australia include olivine-leucite lamproites (≤10 wt% MgO) containing olivine and leucite microphenocrysts, and diamondiferous olivine lamproites (20–30 wt% MgO) containing olivine phenocrysts and larger (1–10 mm) olivine as mantle xenocrysts and dunite micro-xenoliths. Olivine phenocrysts and thin (<100 μm) magmatic rims define trends of decreasing Cr and Ni, and increasing Ca and Mn, with decreasing olivine Mg#, consistent with fractional crystallisation of olivine (and minor chromite). Many phenocrysts are zoned, and those with cores of similar Mg# and trace element abundances to the mantle xenocrysts may be xenocrysts overgrown by later olivine crystallised from the lamproite magma. Magmatic olivines Mg#_91–92 are estimated to have been in equilibrium with olivine lamproite magma(s) containing ~22–24 wt% MgO. The xenocrystic mantle olivines Mg_90–92.5 in the olivine lamproites are inferred from trace element abundances to be mostly derived from garnet peridotite with equilibration temperatures estimated from the Al-in-olivine thermometer (Bussweiler et al. 2017) to be ~1000–1270 °C at depths of 115–190 km. Olivines from the deeper lithosphere are less depleted (lower Mg#, higher Na, Al, P, Ti, Zr etc) than those at shallower depths, a feature suggested to reflect the combined effects of metasomatic re-enrichment of the craton roots (Ti, Fe, Zr etc) and increasing temperature with depth of origin (Na, Al, Ca). The West Kimberley lamproite olivines are not enriched in Li, as might be expected if their source regions contained continental sedimentary material as has been previously inferred from lamproite large-ion-lithophile trace elements, and Sr and Pb isotopes.

     

Der petrogenetische Werdegang der Klinopyroxene in den tertiären Vulkaniten der Hocheifel

The course of crystallization of basalt forming clinopyroxenes in the olivine-basalt-hawaiite-mugearite-trachyte-and basanitoid (= basanite)-series from the Hocheifel area (Western Germany) has been presented by the author in two earlier papers (Hucken-holz, 1965 a, 1965 b). The present paper deals with the evolution of clinopyroxenes from the ankaramites in the same area. The ankaramites are richer in olivines and clinopyroxenes than the normal olivine basalts and may be a product of accumulation of olivines and clinopyroxenes in an olivine basalt magma. The first clinopyroxene formed in the ankaramites is a greenish chromian salite Ca_47.1 Mg_40.9 Fe_12.0 which is preserved in the cores of the phenocrysts. Strongly zoned brown titansalite Ca₄₅ Mg₄₂Fe₁₃ surrounds the chromian salite (HF 5) or appears in independent microphenocrysts (HF53). The groundmass clinopyroxene is titansalite Ca₄₅Mg₃₇Fe₁₈ with a small optic axial angle. Phenocrysts of nickel-rich olivine Fe_12–14 and chrome spinell were formed together with chromium clinopyroxene. The same minerals together with orthopyroxenes have been observed in the olivine basalts, hawaiites and basanitoids (= basanites). This paragenesis indicates high pressure and high temperature in the alkali basalts of the Hocheifel during an initial stage of magmatic evolution. With the decrease of pressure, mineral reaction occurred with the alkali basalt melt. The high pressure clinopyroxenes of the ankaramites and basanitoids (= basanites) were changed to a larger extent than the clinopyroxenes of the olivine basalts and hawaiites or were completely destroyed (HF 53) because they are in contact with the hot magma for a longer period of time. This favours the reaction between the solids and the melt, and the high pressure garnet and/or enstatite components in the clinopyroxenes are substituted by Ca-Tschermak’s and titanaugite molecules.      

攀西裂谷南段鸡街碱性超基性岩矿物学与岩石化学

对攀西裂谷南段云南鸡街碱性超基性岩的岩相学、矿物化学和岩石化学进行了详细研究。单斜辉石和霞石是该岩体的主要造岩矿物,两者互为消长,在霞霓钠辉岩、霓霞岩和磷霞岩中以不同比例组合。辉石多见环带结构,辉石包裹橄榄石的包裹结构和反应边结构发育,共同指示岩浆的快速侵入结晶过程。橄榄石捕掳晶的Fo=75.43～77.42,明显高于同期结晶橄榄石的Fo值(72.02～72.95),可初步判定母岩浆经历了早期的橄榄石分异。通过对全岩主要化学成分及相关组合参数(M、CA、AR、SI、DI)的研究,判定母岩浆系钠质强碱性Si不饱和岩浆。在Harker图解上MgO与其他氧化物均呈良好的相关关系,指示岩浆演化过程中经历了橄榄石和单斜辉石控制的分离结晶作用。lgSI与主量氧化物成分间具有良好的相关关系,指示岩浆演化过程中很少或未受到大陆地壳混染作用。