Petrographic and chemical characterization of igneous lithic clasts from mesosiderites and howardites and comparison with eucrites and diogenites

Combined petrographic, electron microprobe and instrumental neutron activation analysis (INAA) studies of igneous lithic clasts separated from mesosiderites and howardites and INAA investigation only of whole rock eucrites and diogenites have been performed to help elucidate the differentiation processes that occurred on asteroidal sized bodies. Although similar to eucrites in mineralogy and major element chemistry, trace element abundances in basaltic lithic clasts give evidence for more complex differentiation episodes than have been observed for eucrites. These complex fractionations include sequential melting and expulsion of liquid from the source region and remelting of cumulate materials, followed by a second fractional crystallization episode. Rare earth element (REE) abundances in a basaltic clast from Petersburg suggest that the source region which produced this melt was noticably different from that which produced the eucrites Pasamonte and Bereba.Pyroxenites from mesosiderites show slight enrichments in Sc and Mn when compared with average diogenites. This suggests that the pyroxenites in mesosiderites are not fragments of diogenites sensu stricto. A plagioclase clast from the Johnstown diogenite contains light REE abundances that are not in equilibrium with the pyroxene phase. This implies that some of the plagioclase in diogenites may be a foreign component not directly related to the diogenites. This component probably formed on the same parent body as the diogenites however.The characteristics which are inferred for the heat source are that it was spatially and temporally variable. This suggests that heating of the differentiated meteorite parent bodies may in part have been from outside the parent body.     

Metamorphic reactions in mesosiderites: origin of abundant phosphate and silica

The high modal abundances of merrillite [Ca₃(PO₄)₂] and tridymite in most mesosiderites are not the result of igneous fractionation but are attributed to redox reactions between silicates and P-bearing Fe-Ni metal within a limited T-fO₂ range at low pressure. The Emery mesosiderite is the most tridymite- and merrillite-rich mesosiderite so it is used as the model for this study. Examination of reactions in the system CaO-SiO₂-MgSiO₃-Fe-P-O indicate that essentially all of the present phosphorus in Emery should have been dissolved in the metallic portion (calculated to have contained 0.65 wt% P originally), and that it largely reacted to form phosphate. The thermodynamic calculations predict that the reactions would have occurred between 970°C, log fO₂ = ?16.5 and 1030°C, log fO₂ = ?15.0 for the range of phase compositions in Emery. A narrower range of conditions is expected for other mesosiderites. Phosphide (schreibersite) formed only later at temperatures < 600°C during slow cooling. The recalculated amounts of dissolved P and S in the metallic portion of Emery reduce the temperature of the metal liquidus to < 1350°C and the solidus to < 800°C. Thus mixing of liquid metal with cold silicates near the parent body's surface would not have resulted in substantial melting of the silicates but would have resulted in their metamorphism, which is consistent with the textural relationships observed in Emery. This scenario of redox reactions and redistributions of components between metal and silicates represents a new insight into the complexities of mesosiderite processing that helps unravel the mesosiderite history and recalculate their original components.     

L'Olivine dans les howardites: origine,et implications pour le corps parent de ces météorites achondritiques

Electron microprobe analyses have been performed on 300 olivine grains found in 11 howardites. The olivine compositions almost continuously range from Fa 8 to Fa 89 with two prominent populations at Fa 13 and Fa 30. The tail of the fayalite contents distribution may correspond to the succession of several small clusters of Fe-rich olivine grains. Most howardites have olivine populations in common that would result from the fragmentation of different rocks of the howardites parent body. The distribution of the olivine grains between several groups of different $\text{FeO}\text{MnO}$ ratios indicates olivine crystallization from distinct magmas. The chemical characteristics of the olivines of the pallasites, diogenites and mesosiderites are found among the olivines of the howardites and suggests a common parent body for these different types of meteorites. The differentiation model of the eucrites parent body proposed by Stolper (1977) is extended to the partial fusion of distinct assemblages silicates + metal which could proceed from recrystallizations, under different oxidation-reduction conditions, of a primordial chondritic material depleted in volatile elements.     

Uranium and thorium in achondrites

The abundances of U and Th in 19 achondrites and two pallasite olivines have been measured by radiochemical neutron activation analysis. Brecciated eucrites are enriched relative to chondrites in both elements by factors between 10 and 20, perhaps as a result of a magmatic differentiation process. Two unbrecciated eucrites are far less enriched, possibly due to their origin as igneous cumulates. The diogenites Johnstown and Shalka contain approximately chondritic levels of U and Th, but Ellemeet is 10 times lower. The abundances in three howardites are in good agreement with those expected from major element data for a mixing model with eucrite and diogenite end members. The high O¹⁸ basaltic achondrites Nakhla, Shergotty and Angra dos Reis have a range of U and Th abundances similar to the brecciated eucrites and howardites, but have systematically higher Th/U ratios. The Bishopville aubrite has U and Th abundances and Th/U ratios similar to those of several enstatite chondrites, suggesting a genetic relationship. The Norton County aubrite has a low Th/U, similar to that observed in recrystallized and metamorphosed terrestrial ultrabasic rocks, indicating a more complex history. Pallasite olivines have low U and Th contents (0.5.4 ppb and 1.4.3 ppb, respectively) similar to those in terrestrial dunites. The Goalpara ureilite has very low U (<0–6 ppb) and Th (2.7 ppb) abundance consistent with an origin from carbonaceous chondrites by partial melting.     

Petrology, Mineralogy and Geochemisty of Antarctic Mesosiderite GRV 020175: Implications for Its Complex Formation History

<正>GRV 020175 is an Antarctic mesosiderite,containing about 43 vol%silicates and 57 vol% metal.Metal occurs in a variety of textures from irregular large masses,to veins penetrating silicates, and to matrix fine grains.The metallic portion contains kamacite,troilite and minor taenite.Terrestrial weathering is evident as partial replacement of the metal and troilite veins by Fe oxides.Silicate phases exhibit a porphyritic texture with pyroxene,plagioclase,minor silica and rare olivine phenocrysts embedded in a fine-grained groundmass.The matrix is ophitic and consists mainly of pyroxene and plagioclase grains.Some orthopyroxene phenocrysts occur as euhedral crystals with chemical zoning from a magnesian core to a ferroan overgrowth;others are characterized by many fine inclusions of plagioclase composition.Pigeonite has almost inverted to its orthopyroxene host with augite lamellae, enclosed by more magnesian rims.Olivine occurs as subhedral crystals,surrounded by a necklace of tiny chromite grains(about 2-3μm).Plagioclase has a heterogeneous composition without zoning. Pyroxene geothermometry of GRV 020175 gives a peak metamorphic temperature(～1000℃) and a closure temperature(～875℃).Molar Fe/Mn ratios(19-32) of pyroxenes are consistent with mesosiderite pyroxenes(16-35) and most plagioclase compositions(An_(87.5_96.6)) are within the range of mesosiderite plagioclase grains(An_(88-95)).Olivine composition(Fo_(53.8)) is only slightly lower than the range of olivine compositions in mesosiderites(Fo_(55-90)).All petrographic characteristics and chemical compositions of GRV 020175 are consistent with those of mesosiderite and based on its matrix texture and relatively abundant plagioclase,it can be further classified as a type 3A mesosiderite.Mineralogical, penological,and geochemical studies of GRV 020175 imply a complex formation history starting as rapid crystallization from a magma in a lava flow on the surface or as a shallow intrusion.Following primary igneous crystallization,the silicate underwent varying degrees of reheating.It was reheated to 1000℃,followed by rapid cooling to 875℃.Subsequently,metal mixed with silicate,during or after which,reduction of silicates occurred;the reducing agent is likely to have been sulfur.After redox reaction,the sample underwent thermal metamorphism,which produced the corona on the olivine, rims on the inverted pigeonite phenocrysts and overgrowths on the orthopyroxene phenocrysts,and homogenized matrix pyroxenes.Nevertheless,metamorphism was not extensive enough to completely reequilibrate the GRV 020175 materials.     

Chemical evidence for the genesis of the ureilites, the achondrite Chassigny and the nakhlites

Major element and REE, Cr, Sc, V, Ni, Co, Ir, Au, Sr, Ba abundances were determined in three ureilites and the unique achondrite, Chassigny. Chondritic-normalized REE abundance patterns for the ureilites are v-shaped, similar to pallasites, indicating a possible deep-seated origin. The lithophile trace element abundances and v-shaped REE patterns of the ureilites are consistent with a two-stage formation process, the first of which is an extensive partial melting of chondrite-like matter to yield ureilite precursors in the residual solid, which is enriched in Lu relative to La. The second step consists of an admixture of small and variable amounts of material enriched in the light REE. Such contaminating material may be magmas derived from the first formed melt of partial melting of chondrite-like matter.

In contrast to the ureilites, Chassigny has a chondritic-normalized REE pattern which decreases smoothly from La(1.8 × ) to Lu(0.4 × ) and is parallel to and ˜0.25 × the REE pattern in the nakhlitic achondrites. The composition of the magma from which Chassigny crystallized was highly enriched in the light REE; e.g. chondritic normalized La/Lu ˜ 7. The similarity in the fractionated REE patterns (no Eu anomalies) for the olivine-pyroxene Chassigny and for the nakhlites suggests a genetic relationship.

Siderophile trace element relationships in ureilites can be interpreted by three components: (1) ultramafic silicates enriched in Co relative to Ni, (2) an indigenous metal phase remaining after the partial melting event, and (3) a component of the carbon-rich vein material added after the partial melting.     

Metasomatic alterations of olivine inclusions in the Budulan mesosiderite

Mesosiderites are thermal metamorphic breccias consisting of fragments of pyroxene-plagioclase rocks and FeNi metal. The silicate constituent of mesosiderites has a chemical and oxygen isotopic composition analogous to those of meteorites of the HED group: howardites, eucrites, and diogenites. The hypothesis currently most widely accepted for the genesis of mesosiderites is the impact mixing of the material of a differentiated asteroid and an iron meteorite. In contrast to many other classes of meteorites, mesosiderites exhibit no traces of metasomatic processes. The Budulan mesosiderite is the first meteorite of this type in which traces of metasomatism under the effect of an anhydrous fluid were detected. The metasomatic alterations are manifested as chemical zoning of olivine, aggregates of secondary minerals, and the mobilization and redeposition of iron and nickel in the form of metals and sulfides. These alterations were most probably caused by a reaction of olivine with S- and/or CO-bearing gases of endogenic or supergenic provenance. Traces of such metasomatic alterations were previously found in some meteorites and lunar rocks, and these processes could likely play a certain role in the differentiation of chondritic bodies.     

Intrinsic oxygen fugacities of diogenites and mesosiderite clasts

Oxygen fugacities of diogenite and mesosiderite clast material were measured with the double ZrO₂ cell technique between 800° and 1150°C. The samples were taken from large clasts in the diogenites Johnstown (En₇₃) and Tatahouine (En₇₅), and the mesosiderites Estherville (En₈₁), West Point (Fo₈₈) and Emery (En₆₈). Fugacity values for all except Emery plot near the wüstite-iron buffer curve and are interpreted as indicating similar source regions and environments of crystallization for the two suites. Emery orthopyroxene records a lower fugacity, close to the fayalite-quartz-iron buffer curve, probably as a result of equilibration with the mesosiderite matrix assemblage. The similarity of redox conditions experienced by mesosiderite orthopyroxenite and diogenites is not sufficient to require a single parent body and, if the common achondrites were derived from Vesta, mesosiderites probably came from a different body.     

Mesosiderites—I. Compositions of their metallic portions and possible relationship to other metal-rich meteorite groups

The metal from 17 mesosiderites has been analyzed for Ni, Ga, Ge and Ir by the techniques of atomic-absorption spectrometry and neutron activation. Most mesosiderite metal samples fall in a narrow compositional range: Ni, 7·0–9·0 per cent; Ga, 13–16 ppm; Ge, 47–58 ppm; and Ir, 2·4–4·4 ppm. Most of those falling outside these ranges belong to Powell's (1971) least-metamorphosed type. Mesosiderite metal falls in the same general composition range as IIIAB irons, IIIE irons, pallasites and H-group chondrite metal. There are distinct differences in detail, however, and firm evidence for a close genetic relationship between any of these groups and the mesosiderites is lacking. Metallic portions of Weekeroo-type irons tend to have slightly higher Ni, Ga, Ge and Ir contents than found in mesosiderite metal, and the two groups tend to form a single trend on all plots. The Weekeroo-type silicates closely resemble mesosiderites in terms of orthopyroxene composition and oxygen-isotope ratio. We interpret these similarities to indicate that the silicate and metallic portions of these two groups are closely related; if the mesosiderite silicates and metal were initially formed in separate parent bodies, these were of similar composition and formed at about the same distance from the Sun.     

Orthopyroxene-olivine assemblages in diogenites and mesosiderites

Diogenites contain equilibrated orthopyroxene-olivine assemblages. Mn is very regularly partitioned between olivine and orthopyroxene in pallasites, diogenites and synthetic eucrite melts, with an $\text{FeO}\text{MnO}$ partition ratio for olivine versus orthopyroxene of 1.6 by weight over a very wide range of FeO contents. In contrast to diogenites, Fe and Mn are not regularly partitioned between the olivine and orthopyroxene of mesosiderites and these minerals were not in equilibrium. Mesosiderite olivine differs from diogenite olivine in $\text{Fe}\text{Mn}$ and $\text{Ca}\text{Mn}$ ratios. Lack of olivine-orthopyroxene equilibrium suggests that olivine in mesosiderites was derived not from a pyroxenite component analogous to diogenites but from dunites.     

Composition and evolution of the eucrite parent body: evidence from rare earth elements

Eucrites are extraterrestrial plagioclase-pigeonite basalts. Experimental studies suggest that they were produced by partial melting of an olivine (Fo₆₅)-pigeonite (Wo₅En₆₅)-plagioclase (An₉₄)-spinel-metal source region. Quantitative modeling of the evolution of REE abundances in the eucrites indicates that the main group of eucrites (e.g. Juvinas) may be produced by approximately 10% equilibrium partial melting of a source region with initial REE abundances which were chondritic relative and absolute. Other eucrites appear to represent greater (e.g. Sioux County—15%) or smaller (e.g. Stannern—4%) degrees of melting. Moore County and Serra de Magé appear to be cumulates of pyroxene and plagioclase produced by fractional crystallization of a Juvinas-like melt. Nuevo Laredo may represent a residual liquid after such fractional crystallization. Our calculations are consistent with the conclusion that the eucrites were derived from a single type of source region. The close correspondence of the age of the eucrites (? 4.6 AE) to the age of the solar system appears to preclude the possibility of extensive chemical differentiation of the eucrite parent body prior to the event which produced the eucritic melts. Thus our calculations have yielded not only the mode of the source region but, assuming homogeneous accretion, the mode and hence the bulk composition of the eucrite parent body as well. We are unable to estimate quantitatively the ratio of metal to olivine in the parent body. If no metal is present, the bulk composition (in oxide wt%) is Na₂O—0.04, MgO—29.7, Al₂O₃—1.8, SiO₂—39.0, CaO—1.2, FeO—28.3. If, in contrast, the parent body contained 30% metal, the bulk composition of the silicate portion of the eucrite parent body is Na₂O—0.06, MgO—28.0, Al₂O₃—2.6, SiO₂—41.3, CaO—1.9, FeO—26.3. Relative abundances of the meteorites suggest that the eucrite parent body is still intact. The solar system object most closely resembling the eucrites is asteroid 4 Vesta. Because Vesta is unique among the asteroids, we have license to conclude that it is the source of the eucrites and its bulk composition is close to the analyses given above.     

A study of rare earth element (REE)–SiO2 variations in felsic liquids generated by basalt fractionation and amphibolite melting: a potential test for discriminating between the two different processes

The origin of felsic magmas (>63% SiO₂) in intra-oceanic arc settings is still a matter of debate. Two very different processes are currently invoked to explain their origin. These include fractional crystallization of basaltic magma and partial melting of lower crustal amphibolite. Because both fractionation and melting can lead to similar major element, trace element and isotopic characteristics in felsic magmas, such lines of evidence have been generally unsuccessful in discriminating between the two processes. A commonly under-appreciated aspect of rare earth element (REE) solid–liquid partitioning behavior is that D _REE for most common igneous minerals (especially hornblende) increase significantly with increasing liquid SiO₂ contents. For some minerals (e.g., hornblende and augite), REE partitioning can change from incomptatible (D < 1) at low liquid SiO₂ to compatible (D > 1) at high liquid SiO₂. When this behavior is incorporated into carefully constrained mass-balance models for mafic (basaltic) amphibolite melting, intermediate (andesitic) amphibolite melting, lower or mid to upper crustal hornblende-present basalt fractionation, and mid to upper crustal hornblende-absent basalt fractionation the following general predictions emerge for felsic magmas (e.g., ∼63 to 76% SiO₂). Partial melting of either mafic or intermediate amphibolite should, regardless of the type of melting (equilibrium, fractional, accumulated fractional) yield REE abundances that remain essentially constant and then decrease, or steadily decrease with increasing liquid SiO₂ content. At high liquid SiO₂ contents LREE abundances should be slightly enriched to slightly depleted (i.e., C _l/C _o ∼ 2 to 0.2) while HREE abundances should be slightly depleted (C _l/C _o ∼ 1 to 0.2). Lower crustal hornblende-bearing basalt fractionation should yield roughly constant REE abundances with increasing liquid SiO₂ and exhibit only slight enrichment (C _l/C _o ∼ 1.2). Mid to upper crustal hornblende-bearing basalt fractionation should yield steadily increasing LREE abundances but constant and then decreasing HREE abundances. At high liquid SiO₂ contents LREE abundances may range from non-enriched to highly enriched (C _l/C _o ∼ 1 to 5) while HREE abundances are generally non-enriched to only slightly enriched (C _l/C _o ∼ 1 to 2). Hornblende-absent basalt fractionation should yield steadily increasing REE abundances with increasing liquid SiO₂ contents. At high SiO₂ contents both LREE and HREE are highly enriched (C _l/C _o ∼ 3 to 4). It is proposed that these model predictions constitute a viable test for determining a fractionation or amphibolite melting origin for felsic magmas in intra-oceanic arc environments where continental crust is absent. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.

Olivines and olivine coronas in mesosiderites

Olivines and their surrounding coronas in mesosiderites have been studied texturally and compositionally by optical and microprobe methods. Most olivine is compositionally homogeneous but some is irregularly zoned. It ranges from Fo_58–92 and shows no consistent pattern of distribution within and between mesosiderites. Olivine occurs as large single crystals or as partially recrystallized mineral clasts, except for two lithic clasts. One is in Emery, the other in Vaca Muerta, and they are both shock-modified olivine orthopyroxenites. $\text{FeO}\text{MnO}$ ratios in olivine exhibit a variety of differing trends and range from 22–46, most commonly 35–40. These values are lower than those in olivine from diogenites sensu stricto (45–50) and have therefore experienced a different history. Some of the olivine clasts could have coexisted with some of the large orthopyroxene clasts as equilibrium assemblages, but some could not. Much of the olivine may be derived from mesosiderite olivine orthopyroxenites, which differ from diogenites sensu stricto. More magnesian olivine may be a residue from one or more source rocks, with varying degrees of melting. These events probably occurred in a highly evolved and differentiated parent body.Fine-grained coronas surround olivine, except for those in impact-melt group mesosiderites (Simondium, Hainholz, Pinnaroo) and those without tridymite in their matrices (Bondoc, Veramin). Coronas consist largely of orthopyroxene, plagioclase, clinopyroxene, chromite, merrillite and ilmenite and are similar to the matrix, but lack metal and tridymite. Coronas contain abundant orthopyroxene but are unusually rich in chromite (up to 7%) and merrillite (up to 20%). The outer parts of the corona grade into the matrix, but have little or no metal and tridymite. Texturally the innermost part of the corona can be divided into three stages of development: I Radiating acicular; II Intermediate; III Granular. Stage I is the result of the greatest disequilibrium between olivine and matrix orthopyroxene and Stage III has the least disequilibrium. Coronas are the result of the reaction olivine + tridymite = orthopyroxene, probably because FeO (and MgO) diffuse from olivine to tridymite in the matrix. Absence of metal and concentration of chromite in the corona are probably the result of an FeO potential gradient away from the olivine. Merrillite concentrations are a result of P₂O₅ migration into the corona but are controlled by the availability of calcic pyroxene, or possibly plagioclase. Although the coronas are texturally similar to terrestrial and lunar counterparts, they are unique and represent different kinds of reactions marked by a large degree of intra-corona diffusion under dry conditions. Opaque oxide-silicate-metal buffer assemblages yield apparent equilibration conditions of about 840°C and fO₂ near 10^?20. Poikiloblastic pyroxene textures in some coronas suggest a closing of reaction systems between 900 and 1000°C and such systems may record a higher temperature stage of development.     

Rare earth element geochemistry and petrogenesis of miles (IIE) silicate inclusions

An ion probe study of rare earth element (REE) geochemistry of silicate inclusions in the Miles IIE iron meteorite was carried out. Individual mineral phases among inclusions have distinct REE patterns and abundances. Most silicate grains have homogeneous REE abundances but show considerable intergrain variations between inclusions. A few pyroxene grains display normal igneous REE zoning. Phosphates (whitlockite and apatite) are highly enriched in REEs (50 to 2000 × CI) with a relatively light rare earth element (LREE)-enriched REE pattern. They usually occurred near the interfaces between inclusions and Fe host. In Miles, albitic glasses exhibit two distinctive REE patterns: a highly fractionated LREE-enriched (CI normalized La/Sm ∼15) pattern with a large positive Eu anomaly and a relatively heavy rare earth element (HREE)-enriched pattern (CI-normalized Lu/Gd ∼4) with a positive Eu anomaly and a negative Yb anomaly. The glass is generally depleted in REEs relative to CI chondrites.The bulk REE abundances for each inclusion, calculated from modal abundances, vary widely, from relatively depleted in REEs (0.1 to 3 × CI) with a fractionated HREE-enriched pattern to highly enriched in REEs (10 to 100 × CI) with a relatively LREE-enriched pattern. The estimated whole rock REE abundances for Miles are at ∼ 10 × CI with a relatively LREE-enriched pattern. This implies that Miles silicates could represent the product of a low degree (∼10%) partial melting of a chondritic source. Phenocrysts of pyroxene in pyroxene-glassy inclusions were not in equilibrium with coexisting albitic glass and they could have crystallized from a parental melt with REEs of ∼ 10 × CI. Albitic glass appears to have formed by remelting of preexisting feldspar + pyroxene + tridymite assemblage. Yb anomaly played an important role in differentiation processes of Miles silicate inclusions; however, its origin remains unsolved.The REE data from this study suggest that Miles, like Colomera and Weekeroo Station, formed when a molten Fe ball collided on a differentiated silicate regolith near the surface of an asteroid. Silicate fragments were mixed with molten Fe by the impact. Heat from molten Fe caused localized melting of feldspar + pyroxene + tridymite assemblage. The inclusions remained isolated from one another during subsequent rapid cooling.     

Geochemical Constraints of Sediments on the Provenance, Depositional Environment and Tectonic Setting of the Songliao Prototype Basin

The geochemistry of sediments is primarily controlled by their provenances, and different tectonic settings have distinctive provenance characteristics and sedimentary processes. So, it is possible to discriminate provenances, depositional environments and tectonic settings in the development of a sedimentary basin with the geochemistry of the clastic rocks. The analytical results of the present paper demonstrate that sediments in the Songliao prototype basin are enriched in silica (SiO2=66.48-80.51 %), and their ΣREE are 30-130 dmes of that of chondrite with remarkable Eu anomalies. In discriminating diagrams of Eu/Eu vs eeeeeREE and (La/Yb)N vs ΣREE, most samples locate above the line Eu/ Eu=l, on the right of the line Eu/Eu/ΣREE=1 and under the line La/Yb)N/eeeeeREE=1/8, which indicates that the depositional environment of sediments in the basin was oxidizing. In addition, variations of MgO, TiO2, A12O3, FeO+Fe2O3, Na2O and CaO vs SiO2 reflect a tendency of increasing mineral maturity of sediments     

Major Element Compositions and Rare—earth Element Abundaces of Cenozoic Basalts in Eastern China：Implications for a Pressure Control over LREE／HREE Fractionation in Continental Basalt

Major element compositions and rare-earth element (REE) and transition element(Ni,Cr and V) abundances have been determined on 44 basalt samples from eastern China.These basalts have SiO2 contents ranging from 38.63 to 55.24(wt.%),and Na2O K2O from 3.1 to 9.4(wt.%).Ni and Cr abundances are largely variable,respectively falling in ranges 60-605 and 78-1150 ppm.REE abundances,especially light rare-earth elements(LREE), are highly variable.La/Sm and La/Yb ratios vary 2.8 to 7.6 and 1.8 to 8.1. Although the segregation mainly of olivine and clinopyroxene is requested to account for the vari-able and low MgO,CaO/Al2O3,Cr and Ni characteristic of these basalts studied here,the differ-ences in REE composition of the basalts are still related mainly to the partial melting process.Obvious varations in REE abundances could be principally attributed to the partial melting process.Obvious variations in REE abundances could be principally attributed to the partial melting processes that took place at different depths,in spite of some variations caused by the fractional crystallization processes.REE abundances and La/Sm and La/Yb ratios systematically decrease with increasing SiO2,which probably indicated that the basaltic magma derived from a deeper level has higher LREE and LREE/HREE ratios than that from a shallower level.As viewed from the fact that the D^Yb/D^La ratios of clinopyroxenes in the basaltic system increase with increasing pressure,the increase of LREE/HUEE ratios with increasing melting depth can be interpreted as the pressure dependence of bulk D^HREE/D^LREE ratios of silicate minerals,in addition to the pressure control over the melting degree.     

Geochemistry and petrogenesis of the mandidarla volcanics,northwestern Himalayas

The Proterozoic Mandi-Darla Volcanics (MDV) occur as flows intercalated with the low-grade metasediments of the Sundarnagar Group of the Lesser Himalayas. These volcanics are aphyric and have quenched textures with plagioclase-clinopyroxene skeletal microphenocrysts. They are of tholeiitic composition, and are enriched in FeO^t, TiO₂, incompatible trace and rare earth elements. They have relatively high SiO₂ abundances for their MgO levels, which are attributed to high PH₂O pertaining during melt generation. Fractional crystallisation does not appear to have played any major role in the evolution of their bulk chemistry. Instead, they appear to have been generated by different extents of isobaric partial melting of a non-pyrolitic and heterogeneous source with enriched and variable Fe/Mg ratios. REE modelling suggests that the REE enriched source consisted of variable proportions of at least two end members differing in their MREE and HREE contents, but with similar LREE abundances. The enrichment of the source is attributed to mantle metasomatism by a melt-dominated phase penecontemporaneous with magma generation.     

Experimental petrology of eucritic meteorites

Low pressure melting experiments on eucritic meteorites demonstrate that the compositions of most eucrites can be generated by low pressure fractionation of pigeonite and plagioclase from liquids similar in composition to the Sioux County and Juvinas eucrites. It is unlikely that the liquids with compositions similar to Sioux County and Juvinas were themselves residual liquids produced by extensive fractionation of more magnesian parental liquids. The compositions of Stannern and Ibitira cannot be produced by fractionation of liquids with compositions similar to other known eucrites. Liquid compositions similar to Stannern, Ibitira, and Sioux County could have been generated by increasing degrees of low pressure partial melting of source regions composed of olivine (~Fo65), pigeonite (~Wo5En65), plagioclase (~An94), Cr-rich spinel, and metal. These source assemblages may have been primitive, undifferentiated material of the basaltic achondrite parent body and the eucrites may represent melts produced in early stages of its melting and differentiation. Further melting in these source regions, after exhaustion of plagioclase, may have produced magnesian liquids from which the magnesian pyroxenes and olivines in howardites, diogenites, and mesosiderites crystallized in closed-system plutonic environments. Most of the cumulate eucrites (e.g. Moama, Moore County, Serra de Magé) could not have equilibrated with liquids similar in composition to known eucrites. These cumulates may have accumulated from liquids produced by extensive fractionation of advanced partial melts of the source regions of eucritic liquids. A depletion in Na, K, and Rb in Ibitira is noted.     

Rare earth element–SiO<Subscript>2</Subscript> systematics of island arc crustal amphibolite migmatites from the Asago body of the Yakuno Ophiolite,Japan: a field evaluation of some model predictions

The two most commonly invoked processes for generating silicic magmas in intra-oceanic arc environments are extended fractional crystallization of hydrous island arc basalt magma or dehydration melting of lower crustal amphibolite. Brophy (Contrib Mineral Petrol 156:337–357, 2008) has proposed on theoretical grounds that, for liquids >~65 wt% SiO₂, dehydration melting should yield, among other features, a negative correlation between rare earth element (REE) abundances and increasing SiO₂, while fractional crystallization should yield a positive correlation. If correct, the REE–SiO₂ systematics of natural systems might be used to distinguish between the two processes. The Permian-age Asago body within the Yakuno Ophiolite, Japan, has amphibolite migmatites that contain felsic veins that are believed to have formed from dehydration melting, thus forming an appropriate location for field verification of the proposed REE–SiO₂ systematics for such a process. In addition to a negative correlation between liquid SiO₂ and REE abundance for liquids in excess of ~65 % SiO₂, another important model feature is that, at very high SiO₂ contents (75–76 %), all of the REE should have abundances less than that of the host rock. Assuming an initial source amphibolite that is slightly LREE-enriched relative to the host amphibolites, the observed REE abundances in the felsic veins fully support all theoretical predictions.     

Aubrites and diogenites: Trace element clues to their origin

We have analyzed by RNAA 25 aubrite and 9 diogenite samples for 13 to 29 siderophile, volatile, and lithophile trace elements. Both meteorite classes show a typically igneous siderophile element pattern, with Ir, Os, Re, Ge more depleted than Au, Ni, Pd, Sb. But aubrites tend to have about 10 × higher abundances (10^?3 ? 10 ^{? 4} × Cl for the first 4 and 10^?2?10^?3 × Cl for the last 4 siderophiles), apparently reflecting smaller metal/silicate distribution coefficients at lowerf(O₂), or less complete segregation of metal. Se is surprisingly abundant in aubrites (up to 0.4 × Cl), but Te is less so ($\text{Se}\text{Te}\text{? 5 × Cl}$), apparently due to its stronger siderophile character. Other volatiles (Ag, Zn, In, Cd, Bi, T1) show depletions intermediate between lunar dunite and the Earth's mantle.Of 7 aubrites analyzed for REE (Ce, Nd, Eu, Tb, Yb, Lu), 6 are depleted in REE (0.08?0.5 × Cl) and 5 show negative Eu anomalies (the exceptions are Bishopville and Mt. Egerton silicate). This supports an igneous origin, as already noted by Boynton and Schmitt (1972). No samples of the complementary, basaltic and feldspathic rocks have been found thus far, but one of our samples of Khor Temiki dark is a candidate for the basalt. It is 5?7 × enriched in REE and only slightly less so in Rb, Cs, and U. Though shocked and enriched in siderophiles to ~0.05 × Cl, it apparently represents a new meteorite class.Three diogenites analyzed for REE show very diverse patterns, from strongly depleted in light REE for Tatahouine (Ce = 0.01 × Cl) to flat for Garland (~2.5 × Cl). The data confirm the trends found by Fukuokaet al. (1977) as well as their interpretations.Factor analysis shows several parallel groupings for aubrites and diogenites: siderophiles (Re, Ir, Os, Pd, Ge), chalcophiles (Se, Te), volatiles (Ag, In, Tl) and incompatibles (U, REE, and Cs or Rb). But there are some differences for elements such as Ni, Sb, Cd, Bi, Au, and Zn, most of which behave more sensibly in aubrites than in diogenites.Several element pairs that differ greatly in volatility (Cs-U, Ge-Ir) correlate closely in aubrites, in approximately Cl-chondrite proportions. These correlations, and other lines of evidence, suggest strongly that aubrites originated by igneous processes in their parent body, not by direct nebular condensation. The source material may have resembled EL chondrites in oxidation state and depletion of refractories, metal, and volatiles.