The compositions of incipient shock melts in L6 chondrites

Microprobe analyses of 33 melt pocket glasses in five L6d and L6e chondrites show them to be chemically varied but typically enriched in the constituents of plagioclase relative to the host meteorites. This enrichment appears to increase with the degree of melting (0–6.5 vol.%), but other chemical variations among the glasses (sodium depletion, reduction of ferrous iron) appear to be unrelated to shock intensity and melt abundance.Chemical trends for melt pocket glasses differ sharply from those reported for chondrules in ordinary chondrites. Thus partial shock melting of chondritic material is an inadequate explanation for the chemical properties of chondrules.     

Characteristics in naturally and experimentally shocked chondrites: A clue to P-T conditions of impacted asteroids

The aim of this study is to compare the experimentally shock-induced features with those in naturally shocked chondrites and to test the feasibility of experimentally calibrating naturally induced features in shocked H- and L-chondrites. Samples of the Jilin chondrite (H5) were experimentally shock-loaded at the following peak pressures: 12, 27, 39, 53, 78, 83, 93 and 133 GPa respectively. Chondritic melts were first obtained at P>78 GPa and more than 60% melting was achieved at P~133 GPa. No high-pressure phases were observed in any of the shocked samples, neither in the deformed nor in the molten regions. Textural relations and mineral assemblages of the shocked samples are comparable to those encountered in the heavily shocked H-chondrite Yanzhuang but differ considerably from those found in heavily shocked L6 chondrites. Shock melt veins in L6 chondrites contain high-pressure polymorphs of olivine and pyroxene and high pressure liquidus phases. Scaling from shock experiments on millimeter-sized samples to natural shock features on kilometer-sized asteroids poses considerable problems in quantifying the P-T conditions during natural shock events on asteroids.     

Petrogenesis of complex veins in the Chantonnay (L6f) chondrite

Two cross-cutting veins in the Chantonnay (L6f) chondrite illustrate different patterns of fractionation of total chondritic shock melts. The earlier vein, which is dark-colored and bears abundant host rock xenoliths, is strongly reduced and sodium-poor relative to the bulk meteorite. It resembles and may be cogenetic with melt pockets in Chantonnay. The later vein, which is lighter-colored and somewhat vesicular, lacks evidence of either Na loss or reduction but shows modest internal differentiation. Its metal and total iron contents (26.5 wt.%) are higher than normal for L-group chondrites.The trend of chemical fractionation recorded in the earlier Chantonnay vein resembles that reported for chondrules in ordinary chondrites, suggesting that chemical variations among chondrules in part reflect variations among their parental shock melts.     

Fine-grained aggregates in L3 chondrites

The textures and chemical compositions of the constituent minerals of the fine-grained aggregates (FGA's) of L3 chondrites were studied by the backscattered electron image technique, electron probe microanalysis, and transmission electron microscopy. Plagioclase and glass in the interstices between fine grains of olivine and pyroxene indicate that the FGA's once partly melted. Compositional zoning and decomposition texture of pyroxenes are similar to those observed in chondrules, indicating a common cooling history of the FGA's and chondrules. Therefore, the mechanism that caused melting of the FGA's is considered to be the same as for chondrules. Bulk compositions of the FGA's are within the range of those of chondrules, so some chondrules probably were produced by complete melting of the same precursor materials as those of the FGA's. The precursor materials must have included fine olivine and other grains that probably are condensates.     

Petrogenesis of basalts from the project FAMOUS area: experimental study from 0 to 15 kbars

Tholeiitic basalt glasses from the FAMOUS area of the Mid-Atlantic Ridge are among the most primitive basaltic liquids reported from the ocean basins. One of the more primitive of these[Mg/(Mg+Fe²⁺) = 0.68;Ni= 232ppm;TiO₂ = 0.61] glasses (572-1-1) was selected for an experimental investigation. This study found olivine to be the liquidus phase from 1 atm to 10.5 kbar where it is replaced by clinopyroxene. The sequence of appearance of phases at 1 atm pressure is olivine (1268°C), plagioclase (1235°C) and clinopyroxene (1135°C). The sample is multiply saturated at 10.5 kbar with olivine (Fo₈₈), clinopyroxene (Wo₃₂En₆₀Fs₉), and orthopyroxene (Wo₅En₈₃Fs₁₂). From the 1-atm data we have measured (FeO/MgO) olivine/(FeO*/MgO) liquid (K′_D) for olivine-melt pairs equilibrated at 12 temperatures in the range 1268–1205°C.K′_D varies from 0.30 at 1205°C to 0.27 at 1268°C. Analysis of high-pressure olivine melt pairs indicates a systematic increase inK′_D with pressure.Evaluation of the 1-atm experiments reveals that fractionation of olivine followed by olivine + plagioclase can generate much of the variation in major element chemistry observed in the FAMOUS basalt glasses. However, it cannot account for the entire spectrum of glass compositions — particularly with respect to TiO₂ and Na₂O. The variations in these components are such as to require different primary liquids.Comparison of clinopyroxene microphenocrysts/xenocrysts found in oceanic tholeiites with experimental clinopyroxenes reveal that the majority of those in the tholeiites may have crystallized from the magma at pressures greater than ～ 10 kbar and are not accidental xenocrysts. Clinopyroxene fractionation at high pressures may be a viable mechanism for fractionating basaltic magmas.The major and minor element mineral/meltK′_d's from our experiments have been used to model the source region residual mineralogy for given percentages of partial melting. These data suggest that ～20% partial melting of a lherzolite source containing 0–10% clinopyroxene can generate the major and minor element concentrations in the parental magmas of the Project FAMOUS basalt glasses.     

Geobarometry of ultramafic xenoliths from Loihi Seamount,Hawaii, on the basis of CO2 inclusions in olivine

Abundant fluid inclusions in olivine of dunite xenoliths (～1–3 cm) in basalt dredged from the young Loihi Seamount, 30 km southeast of Hawaii, are evidence for three coexisting immiscible fluid phases—silicate melt (now glass), sulfide melt (now solid), and dense supercritical CO₂ (now liquid + gas)—during growth and later fracturing of some of these olivine crystals. Some olivine xenocrysts, probably from disaggregation of xenoliths, contain similar inclusions.Most of the inclusions (2–10 μm) are on secondary planes, trapped during healing of fractures after the original crystal growth. Some such planes end abruptly within single crystals and are termed pseudosecondary, because they formed during the growth of the host olivine crystals. The “vapor” bubble in a few large (20–60 μm), isolated, and hence primary, silicate melt inclusions is too large to be the result of simple differential shrinkage. Under correct viewing conditions, these bubbles are seen to consist of CO₂ liquid and gas, with an aggregate ? = ～ 0.5–0.75 g cm^?3, and represent trapped globules of dense supercritical CO₂ (i.e., incipient “vesiculation” at depth). Some spinel crystals enclosed within olivine have attached CO₂ blebs. Spherical sulfide blebs having widely variable volume ratios to CO₂ and silicate glass are found in both primary and pseudosecondary inclusions, demonstrating that an immiscible sulfide melt was also present.Assuming olivine growth at ～ 1200°C and hydrostatic pressure from a liquid lava column, extrapolation of CO₂P-V-T data indicates that the primary inclusions were trapped at ～ 220–470 MPa (2200–4700 bars), or ～ 8–17 km depth in basalt magma of ? = 2.7 g cm^?3. Because the temperature cannot change much during the rise to eruption, the range of CO₂ densities reveals the change in pressure from that during original olivine growth to later deformation and rise to eruption on the sea floor. The presence of numerous decrepitated inclusions indicates that the inclusion sample studied is biased by the loss of higher-density inclusions and suggests that some part of these olivine xenoliths formed at greater depths.     

SiO2 precipitation in olivine: ATEM investigation of two dunites annealed at 300 MPa in hydrous conditions

Two natural dunites were annealed at pressure P=300 MPa, temperature T=1373, 1473 and 1573 K, and fO₂ within the stability field of olivine. The starting materials contained small amounts of hydroxyls in the form of minor phases of hydrated minerals, which released an aqueous phase during the experiments. A detailed analytical transmission electron microscopy (ATEM) investigation of these materials revealed that small quantities of two types of silica-rich glass formed during heat treatment. The first type of glass, found at triple junctions as rare partially crystallized glass pockets, results from melting dehydration reactions involving the hydrous phases. The second type of glass is found as pure silica precipitates (0.1–0.5 μm in size, for a total of a few 0.1 vol%) within the olivine grains of specimens heated to ≥1473 K. From considerations of the kinetics of the precipitation at 1473 K, we interpret this silica precipitation as resulting from the condensation of olivine metallic vacancies promoted by increasing fluid fugacities during the runs. Our observations, thus, demonstrate that metastable silica can precipitate in olivine from dunites experiencing rapid changes in their thermodynamical environment.     

40Ar-39Ar chronology of isolated phases from Bununu and Malvern howardites

High resolution⁴⁰Ar-³⁹Ar age spectra have been measured on plagioclase and glass from two howardites. Both the plagioclase and glass from the gas-rich Bununu howardite show well-defined age plateaux, yielding distinct ages of 4.42 ± 0.04 and 4.24 ± 0.05 AE, respectively. These age patterns are rather well behaved and are interpreted as representing the distinct times of formation of plagioclase from igneous processes and of glass fragments produced by impact on the meteorite body. The release pattern for the glass from the heavily shocked Malvern howardite is undulating at low and intermediate temperatures but does have a high-temperature plateau. Its age spectrum indicates little apparent diffusion loss, but rather an extensive redistribution of either⁴⁰Ar during the shock event or of³⁹Ar during the neutron irradiation or both. The total K-Ar age of Malvern glass is 3.64 ± 0.04 AE and the high-temperature plateau is 3.73 ± 0.05 AE. The age spectrum of the Malvern plagioclase has an intermediate temperature “plateau” at 3.80 AE that represents 20% of the total⁴⁰Ar content and increases towards a high-temperature plateau at 4.29 ± 0.04 AE containing 26% of the total gas release. It seems likely that the event which formed the Malvern glass also reset part of the plagioclase. The distinct histories observed for the different phases of these howardites are consistent with their formation from a regolith. The present results along with similar young ages for igneous clasts from Kapoeta clearly show that the regoliths were extant on the parent bodies of howardites and that they were subjected to violent impact events at least as recently as 3.7 AE ago.     

The Niger (I) carbonaceous chondrite and implications for the origin of aggregates and isolated olivine grains in C2 chondrites

The origin of olivine grains in C2 carbonaceous chondrites is a controversial topic: directly condensed material or detrital remnants of preexisting chondrules? This study shows that the Niger C2 meteorite is similar to Murchison but reveals several interesting features in relation to the origin of the olivine. Microprobe analysis of olivine (Si, Fe, Mg, Ca, Mn, Cr), glass and nickel-iron inclusions within the grains, and Fe-S-O phase as well as the relationships between the olivine grains in the aggregates, between the grains and the interstitial phyllosilicate matrix, between the inclusions and their host olivine grains, and the morphology of some aggregates all show that two populations of olivine coexist, probably crystallized from chondrule melts rather than by direct condensation from a solar nebula gas. The characteristics of the nickel-iron inclusions within the olivine suggest a magmatic chondrule-making stage from previously condensed materials.     

On the origin of isolated olivine grains in type 2 carbonaceous chondrites

The origin of olivine grains isolated in the matrix of C2 carbonaceous chondrites is an important problem. If these grains are condensates from a solar nebular gas, they contain compositional, isotopic and physical features that further elucidate that process. If, however, they are grains released by the breakup of chondrules, then many important condensation features have been lost during the melting that took place to form chondrules.In evaluating these two possibilities, care must be taken to determine which inclusions in C2 meteorites are actual chondrules and which are aggregates of grains that have never undergone melting. The two main types of aggregates, pyroxene-rich and pyroxene-poor, are forty to fifty times more abundant than chondrules. Four scenarios are presented to account for the kinds of aggregates and isolated grains seen in the Murchison C2 meteorite. An analysis of these scenarios is made in light of olivine crystal morphology, comparison of composition of glass inclusions inside olivine grains with interstitial glass in true chondrules and size distributions of olivines, isolated, in aggregates and in chondrules.It is concluded that no scenario that includes a chondrule-making step can account for the observed population of isolated olivine grains. An origin by direct condensation, partial comminution, aggregation and accretion best accounts for the sizes and morphological features observed.     

Potassium-rich volcanic rocks of the Muriah complex, Java, Indonesia: Products of multiple magma sources?

The extinct Pleistocene volcano Muriah, situated behind the main Pleistocene—Recent Sunda magmatic arc in north-central Java, has erupted at least two contrasted groups of lavas. One group forms a well-defined compositional series (Anhydrous Series) from leucite basanite to tephritic phonolite, with olivine and tschermakitic clinopyroxene the main phenocrysts. The other group, the “Hydrous Series”, includes compositionally variable tephrites and high-K andesites with common plagioclase, biotite and amphibole. Lavas of the Anhydrous Series are much richer in LIL trace elements than the most potassic lavas of neighbouring active volcanoes, but relative HFS element enrichment is less pronounced. REE patterns have almost constant slopes from La (250–600 times chondrites) to Yb (5–10 times chondrites), while those of lavas of active centres are less light-enriched, and show flattening in the heavy REE. Anhydrous Series initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043–0.7046) are lower than those of active centres (0.7047–0.7053). Hydrous Series lavas are intermediate in all these geochemical characteristics.The most mafic A-series leucite basanite, with Mg/(Mg + Fe²⁺) 0.69, 140 ppm Ni and 620 ppm Cr was probably derived from the primary magma for the series by fractionation of only 5 wt.% olivine. Its REE pattern suggests derivation from a garnet-bearing source. Experiments on this basanite, with up to 10% olivine and 20% orthopyroxene added, and in the presence of H₂O and H₂O/CO₂ mixtures, have shown that for all but very high magma water contents, the olivine and garnet liquidus fields are widely separated by fields of phlogopite and clinopyroxene. There is no liquidus field of orthopyroxene. Hence, if magma production involved an equilibrium melting process alone, the most probable sources are of garnet-bearing phlogopite clinopyroxenite type. Alternatively, this magma may represent the end-product of interaction between a low-K basanite magma from a garnet lherzolite source in the asthenosphere and a phlogopite-bearing lherzolite zone in the lower lithosphere. Its production was probably related to crustal doming and extension superimposed on the dominant subduction regime. Hydrous Series magmas may have resulted from mixing between Anhydrous Series magmas and high-K calc-alkaline basaltic to andesitic magmas more directly related to subduction processes.     

On the chondrite—achondrite transition: mineralogy and chemistry of Yamato 74160 (LL7)

We report on the petrology, mineralogic properties and contents of major elements and trace elements Ag, Au, Bi, Cd, Co, Cs, Ga, In, Rb, Se, Te, Tl, U and Zn (determined by radiochemical neutron activation analysis) in Yamato 74160, interpreted as an LL7 chondrite. All properties are consistent with this meteorite having been recrystallized and partially melted locally once at temperatures well above 1090°C under conditions such that some minerals (e.g. plagioclase, euhedral pyroxene, tetrataenite) grew from melt pockets and siderophilic and chalcophilic elements were lost by extraction into eutectic melt that drained away. Inhomogeneous plagioclase compositions and mobile element loss suggest shock as the most likely heat source. Yamato 74160, while inferentially chondritic, is a larval achondrite: even higher temperatures and longer times would have been required to cause the separations necessary to transform it to an identifiable achondrite type.     

Chromite in the Paricutin lava flows (1943–1952)

Small euhedral chromite crystals are found in olivine macrophenocrysts (Fo_80–84) from the basaltic andesites (150 ppm Cr) erupted in 1943–1947, and in orthopyroxene macrophenocrysts of the andesites (75 ppm Cr) erupted in 1947–1952. The majority of the chromite octahedra are 5–20 μm in diameter, and some are found in clusters and linear chains of three or more oriented chromite crystals. The composition of the majority of the chromite grains within olivine and orthopyroxene macrophenocrysts is Fe²⁺/(Fe²⁺+Mg)=0.5–0.6, Cr/(Cr+Al)=0.5–0.6 and Fe³⁺/(Fe³⁺+Al+Cr)=0.2–0.3. The chromite crystals in contact with the groundmass are larger, subhedral, and grade in composition from chromite cores to magnetite rims. Comparison of the composition of chromite with those of other volcanic rocks shows that the most primitive Paricutin chromite is richer in total iron and higher in Fe³⁺/(Fe³⁺+Al+Cr) than primary chromite in most lavas. The linear chains of oriented chromite octahedra are found in olivine and orthopyroxene macrophenocrysts, and in the groundmass. These chromite chains are thought to result from diffusion-controlled crystallization because of the very high partition coefficient (1000) of Cr between chromite and melt. We conclude that chromite was a primary phase in the lavas at the time of extrusion and that magnetite only crystallized after extrusion during cooling of the lava flows. The presence of chromite microphenocrysts in andesitic lavas containing as little as 70 ppm Cr can be explained by dissolved H₂O in the melt depressing the liquidus temperature for orthopyroxene such that chromite becomes a liquidus phase. The influence of dissolved H₂O can also explain the lack of plagioclase macrophenocrysts in most of the lavas and the relatively high partition coefficient (20) of Ni between olivine and melt and the high partition coefficient (40) of Cr between orthopyroxene and melt. The liquidus temperature of the basaltic andesite is estimated to have been less than 1140°C, assuming H₂O>1 wt.%, and the log f_O2 to have been above that of the QFM buffer. The chromite and orthopyroxene liquidus temperature of the andesites, assuming H₂O>1 wt.%, is estimated to have been 1100°C or less. The derivation of the later andesites from the earlier basaltic andesites has been explained by a combination of fractional crystallization of olivine, orthopyroxene and plagioclase, and assimilation of xenoliths. The significantly lower Cr, Ni and Mg of the andesites may have been in part due to the separation of olivine macrophenocrysts plus enclosed chromite crystals from the earlier basaltic andesites.     

Textural evidence bearing on the origin of isolated olivine crystals in C2 carbonaceous chondrites

In some cases the mechanical competence of chondrules in carbonaceous chondrites has been reduced by alteration of their mesostasis glass to friable phyllosilicate, providing a mechanism by which euhedral olivines can be separated from chondrules. Morphological features of isolated olivine grains found in carbonaceous chondrites are similar to those of olivine phenocrysts in chondrules. These observations suggest that the isolated olivine grains formed in chondrules, by crystallization from a liquid, rather than by condensation from a vapor.     

Plagioclase ultraphyric basalts in Iceland: the mush of the rift

Glassy, plagioclase ultraphyric basalts from six locations in Iceland have bimodal phenocryst size distributions where microphenocrysts (ol+plg±cpx±mt) are in equilibrium with the matrix glass, but macrophenocrysts (ol+plg±cpx) are too primitive to be so. Matrix glass compositions are similar to those of other rift zone glasses from Iceland, and oxygen isotope variations suggest they interacted with the Icelandic crust. A lack of negative Eu-anomalies in matrix glasses precludes large amounts of plagioclase crystallisation from their parental liquids. Compositions of glass inclusions in plagioclase and olivine macrophenocrysts indicate that parental magma compositions of the macrophenocryst assemblage are similar to those of primitive, Icelandic rift zone glasses. Temperatures for plagioclase macrophenocryst crystallisation obtained from Linkam^® heating stage experiments, and from glass inclusion compositions corrected for post-entrapment crystallisation, give temperatures up to 1260°C, corresponding to crystallisation at middle to deep crustal levels. Temperature differences of less than 100°C between plagioclase-hosted glass inclusions before and after post-entrapment plagioclase crystallisation show that the macrophenocrysts must have been kept at elevated temperatures prior to incorporation in their present host magmas. We suggest that the macrophenocrysts of the plagioclase ultraphyric basalts accumulated in crystal mush bodies underneath the rift zone and were picked up by their present hosts during a rifting event with increased magma supply from the mantle.     

Crystallization of tholeiitic basalt in Alae Lava Lake,Hawaii

The eruption of Kilauea Volcano August 21–23, 1963, left 600,000 cubic meters of basaltic lava in a lava lake as much as 15 meters deep in Alae pit crater. Field studies of the lake began August 27 and include repeated core drilling, measurements of temperature in the crust and melt, and precise level surveys of the lake surface. The last interstitial melt in the lake solidified late in September 1964; by mid August 1965 the maximum temperature was 690°C at a depth of 11.5 meters. Pumice air-quenched from about 1140°C contains only 5 percent crystals — clinopyroxene, cuhedral olivine (Fo ₈₀), and a trace of plagioclase, (An ₇₀). Drill cores taken from the zone of crystallization in the lake show that olivine continued crystallizing to about 1070°C; below that it reacts with the melt, becoming corroded and mantled by pyroxene and plagioclase. Below 1070°C, pyroxene and plagioclase crystallized at a constant ratio. Ilmenite first appeared at about 1070°C and was joined by magnetite at about 1050°C; both increased rapidly in abundance to 1000°C. Apatite first appeared as minute needles in interstitial glass at 1000°C. Both the abundance and index of refraction of glass quenched from melt decreased nearly linearly with falling temperature. At 1070°C the quenched lava contains about 65 percent dark-brown glass with an index of 1.61; at 980°C it contains about 8 percent colorless glass with an index of 1.49. Below 980°C, the percentage of glass remained constant. Progressive crystallization forced exsolution of gases from the melt fraction; these formed vesicles and angular pores, causing expansion of the crystallizing lava and lifting the surface of the central part of the lake an average of 19.5 cm. The solidified basalt underwent pneumatolitic alteration, including deposition of cristobalite at 800°C, reddish alteration of olivine at 700°C, tarnishing of ilmenite at 550°C, deposition of anhydrite at 250°C, and deposition of native sulfur at 100°C. Ferric-ferrous ratios suggest that oxidation with maximum intensity between 550°C and 610°C moved downward in the crust as it cooled; this was followed by reduction at a temperature of about 100°C. The crystallized basalt is a homogeneous fine-grained rock containing on the average 48.3 percent by volume intergranular pyroxene (augite > pigeonite), 34.2 percent plagioclase laths (An_{60 70}), 7.9 percent interstitial glass, 6.9 percent opaques (ilmenite > magnetite), 2.7 percent olivine (Fo_{70 80}), and a trace of apatite. Chemical analyses of 18 samples, ranging from initially quenched pumice to lava cored more than a year after the eruption from the center and from near the base of the lake, show little variation from silica-saturated tholeiitic basalt containing 50.4 percent SiO₂, 2.4 percent Na₂O, and 0.54 percent K₂O. Apparently there was no significant crystal settling and no appreciable vapor-phase transport of these components during the year of crystallization. However, seven samples of interstitial liquid that had been filter-pressed into gash fractures and drill holes from partly crystalline mush near the base of the crust show large differences from the bulk composition of the solidified crust—lower MgO, CaO, and Al₂O₃; and higher total iron, TiO₂, Na₂O, K₂O, P₂O₅, and F, and, in most samples, SiO₂. The minor elements Ba, Ga, Li, Y, and Yb and possibly Cu tend to be enriched in the filter-pressed liquids, and Cr and possibly Ni tend to be depleted.     

Origin of iron-rich olivine in the matrices of type 3 ordinary chondrites: an experimental study

In order to understand the origin of iron-rich olivine in the matrices of type 3 ordinary chondrites, the reaction of metallic iron and enstatite, with and without forsterite and SiO₂, has been experimentally reproduced at temperatures between 1150° and 800°C and P_O2 between 10⁻¹¹ and 10⁻¹⁶ atm (between the IQF and MW buffers). The olivine produced ranges from Fo₅₈ to Fo₃₄ and this composition does not change significantly with temperature and time of the runs. The magnesian olivine which forms does become more magnesian with increasing forsterite/enstatite ratio of the starting materials. Iron-rich olivine (Fo< 35) cannot be formed by the reaction of enstatite and metallic iron, with or without forsterite as starting materials but it can be formed in the presence of free silica. The composition of olivine becomes more iron-rich with increasing silica/enstatite ratio. The compositional range of olivine formed from each mixture is 25–30 mole% Fo regardless of the temperature, composition, mineral assemblage, and run duration.From these experimental results, two possibilities suggested for the origin of the iron-rich olivine in the matrices of type 3 ordinary chondrites: (1) free silica must have been present if the iron-rich olivine was formed by solid-state reactions under oxidizing condition in the solar nebula; (2) reaction of silicon-rich gas with metallic iron took place under oxidizing condition in the solar nebula. Though it is difficult to define which alternative was dominant, the formation of free silica or silicon-rich gas may be a result of fractional condensation. This is possible if there is a reaction relation between forsterite and gas to produce enstatite. The suggested fractional condensation is supported by the fact that the compositions of the fine-grained matrices of type 3 ordinary chondrites are more silica-rich than the bulk compositions of the chondrites. Though it is not known whether such conditions were established all over the nebula or locally in the nebula, both fractionation and more oxidizing conditions than the average solar nebula are required for the formation of matrix olivine.     

Studies of Brazilian meteorites: III. Origin and history of the Angra dos Reis achondrite

The Angra dos Reis meteorite fell in 1869 and is a unique achondrite. It is an ultramafic igneous rock, pyroxenite, with 93% fassaite pyroxene which has 15.7% Ca-Tschermak's molecule, plus calcic olivine (Fo_53.1; 1.3% CaO), green hercynitic spinel, whitlockite (merrillite), metallic Ni-Fe, troilite, as well as magnesian kirschsteinite (Ks_62.3Mo_37.7), within olivine grains, and celsian (Cs_90.2An_7.7Ab_1.7Or_0.4) which are phases reported in a meteorite for the first time, and plagioclase (An_86.0), baddeleyite, titanian magnetite (TiO₂, 21.9%), and terrestrial hydrous iron oxide which are phases reported for the first time in this meteorite. Petrofabric analysis shows that fassaite has a preferred orientation and lineation which is interpreted as being due to cumulus processes, possibly the effect of post-depositional magmatic current flow or laminar flow of a crystalline mush. The mineral chemistry indicates crystallization from a highly silica-undersaturated melt at low pressure. Since the meteorite formed as a cumulate, pyroxene crystals may have gravitationally settled from a melt which crystallized melilite first. Plagioclase would be unstable in such a highly undersaturated melt, and feldspathoids would be rare or absent due to the very low alkali contents of the melt. The presence of rare grains of plagioclase and celsian may be the result of late-stage crystallization of residual liquids in local segregations. Thus, the Eu anomaly in Angra dos Reis may be the result of pyroxene separation from a melt which crystallized melilite earlier, rather than plagioclase as previously suggested.     

Silicate‐oxide mineral chemistry of mafic–ultramafic rocks as an indicator of the roots of an island arc: The Chilas Complex,Kohistan (Pakistan)

The Chilas Complex is a major lower crustal component of the Cretaceous Kohistan island arc and one of the largest exposed slices of arc magma chamber in the world. Covering more than 8000 km², it reaches a current tectonic width of around 40 km. It was emplaced at 85 Ma during rifting of the arc soon after the collision of the arc with the Karakoram plate. Over 85% of the Complex comprises homogeneous, olivine‐free gabbronorite and subordinate orthopyroxene–quartz diorite association (MGNA), which contains bodies of up to 30 km² of ultramafic–mafic–anorthositic association (UMAA) rocks. Primary cumulate textures, igneous layering, and sedimentary structures are well preserved in layered parts of the UMAA in spite of pervasive granulite facies metamorphism. Mineral analyses show that the UMAA is characterized by more magnesian and more aluminous pyroxene and more calcic plagioclase than those in the MGNA. High modal abundances of orthopyroxene, magnetite and ilmenite (in MGNA), general Mg–Fe–Al spatial variations, and an MFA plot of whole‐rock analyses suggest a calc‐alkaline origin for the Complex. Projection of the pyroxene compositions on the Wo–En–Fs face is akin to those of pyroxenes from island arcs gabbros. The presence of highly calcic plagioclase and hornblende in UMAA is indicative of hydrous parental arc magma. The complex may be a product of two‐stage partial melting of a rising mantle diaper. The MGNA rocks represent the earlier phase melting, whereas the UMAA magma resulted from the melting of the same source depleted by the extraction of the earlier melt phase. Some of the massive peridotites in the UMAA may either be cumulates or represent metasomatized and remobilized upper mantle. The Chilas Complex shows similarities with many other (supra)subduction‐related mafic–ultramafic complexes worldwide.     

Chrome spinel in normal MORB‐type greenstones from the Paleozoic–Mesozoic Mino terrane,East Takayama area,central Japan: Crystallization course with a U‐turn

Phenocrystic chrome spinel crystallized in normal MORB‐type greenstones in the East Takayama area. Associated phenocryst minerals show a crystallization sequence that was olivine first, followed by plagioclase, and finally clinopyroxene. Chrome spinel ranges from 0.54 to 0.77 in Mg/(Mg+Fe²⁺) and 0.21 to 0.53 in Cr/(Cr+Al); the Fe³⁺ content varies from 0.07 to 0.22 p.f.u. (O = 4). Significant compositional differences of spinel were observed among the phenocryst mineral assemblages. Chrome spinel in the olivine–spinel assemblage shows a wide range in Cr/(Cr+Al), and is depleted in Fe²⁺ and Fe³⁺. Chrome spinel in the olivine–plagioclase–clinopyroxene–spinel assemblage is Fe²⁺‐ and Fe³⁺‐rich at relatively high Cr/(Cr+Al) ratios. Basalt with the olivine–plagioclase–spinel assemblage contains both aluminous spinel and Fe²⁺‐ and Fe³⁺‐rich spinel. The assumed olivine–spinel equilibrium suggests that chrome spinel in the olivine–spinel assemblage changed in composition from Cr‐ and Fe²⁺‐rich to Al‐ and Mg‐rich with the progress of fractional crystallization. Chrome spinel in the olivine–plagioclase–clinopyroxene–spinel assemblage, on the other hand, exhibits the reversed variations in Mg/(Mg+Fe²⁺) and in Cr/(Cr+Al) ratios that decrease and increase with the fractional crystallization, respectively. The entire crystallization course of chrome spinel, projected onto the Mg/(Mg+Fe²⁺)–Cr/(Cr+Al) diagram, exhibits a U‐turn, and appears to be set on a double‐lane route. The U‐turn point lies in the compositional field of chrome spinel in the olivine–plagioclase–spinel assemblage, and may be explained by plagioclase fractionation that began during the formation of the olivine–plagioclase–spinel assemblage.