Abundance and isotopic composition of noble gases in metal and graphite of the Bohumilitz IAB iron meteorite

Abstract— Abundances and isotopic compositions of noble gases in metal and graphite of the Bohumilitz IAB iron meteorite were measured. The abundance ratios of spallogenic components in metal reveal a ³He deficiency which is due to the diffusive loss of parent isotopes, that is, tritium (Tilles, 1963; Schultz, 1967). The diffusive loss likely has been induced by thermal heating by the Sun during cosmic‐ray exposure (～160 Ma; Lavielle et al, 1999). Thermal process such as impact‐induced partial loss may have affected the isotopic composition of spallogenic Ne. The ¹²⁹Xe/¹³¹Xe ratio of cosmogenic components in the metal indicates an enhanced production of epi‐thermal neutrons. The abundance ratios of spallogenic components in the graphite reveal that it contained small amounts of metal and silicates. The isotopic composition of heavy noble gases in graphite itself was obtained from graphite treated with HF/HCl. The isotopic composition of the etched graphite shows that it contains two types of primordial Xe (i.e., Q‐Xe and El Taco Xe). The isotopic heterogeneity preserved in the Bohumilitz graphite indicates that the Bohumilitz graphite did not experience any high‐temperature event and, consequently, must have been emplaced into the metal at subsolidus temperatures. This situation is incompatible with an igneous model as well as the impact melting models for the IAB‐IIICD iron meteorites as proposed by Choi et al. (1995) and Wasson et al (1980).     

Fluid inclusions in upper mantle xenoliths from Northern Patagonia,Argentina: Evidence for an upper mantle diapir

Summary Three generations of fluid inclusions can be recognized in upper mantle xenoliths from alkali basalts of the Somoncura Massif, Northern Patagonia, Argentina. The first (early, primary) one consists of dense CO₂ inclusions which were trapped in the mantle-crust boundary zone (22–36 km minimum trapping depth). Their co-genetic relationship with silicate melt inclusions enables us to constrain their minimum trapping temperature at 1200°C, indicating a high temperature event in a cooler environment. The late (pseudosecondary and secondary) generations of fluid inclusions were classified in accordance with their homogenization temperature to liquid CO₂ (L1) and vapor CO₂ (L2) phase. The minimum trapping depth for the first of the late inclusions (L1) is about 16 km. In spite of the uncertainties related to this value, L1 inclusions indicate that the upper mantle rocks, of which samples were delivered by the basalts, had some residence time in the middle crust where they experienced a metasomatic event. The fact that this event did not destroy the earlier inclusions, places severe constraints on its duration. The second late inclusions (L2) are low-pressure CO₂ inclusions with a minimum trapping depth of only 2 km, presumably a shallow magma chamber of the host basalts. The succession of fluid inclusions strongly points toward a fairly fast uprising upper mantle underneath Northern Patagonia. The petrology and mineral chemistry of the peridotitic xenoliths support this view. Extensive partial melting and loss of these melts is indicated by the preponderance of harzburgites in the upper mantle underneath Northern Patagonia, a fairly unusual feature for a continental upper mantle. That depletion event as well as several metasomatic events — including those which left traces of fluid inclusions — are possibly related to a high-speed diapiric uprise of the upper mantle in this area. The path can be traced from the garnet peridotite stability field into the middle crust, a journey which must have been unusually fast. Differences in rock, mineral, and fluid inclusion properties between geographic locations suggest a diffuse and differential type of diapirism. Future studies will hopefully help to map the full extent and the highs and lows of this diapir and elucidate questions related to its origin and future.

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Fluid-Einschlüsse in Erdmantel-Xenolithen von Nord-Patagonien: Evidenz für einen Diapir im oberen Erdmantel

Zusammenfassung Erdmantel - Xenolithe in Alkali-Basalten des Somoncure Massivs, Nord-Patagonien, Argentinien, führen drei Generationen von Fluid-Einschlüssen. Die erste (frühe, primäre) Generation besteht aus dichten CO₂-Einschlüssen, welche offenbar in der Mantel-Kruste Grenzzone (22–36 km Minimum-Tiefe) eingeschlossen wurden. CO₂-Einschlüsse sind kogenetisch mit Silikat-Schmelzeinschlüssen. Dies erlaubt die Abschätzung der Einschließ-Temperatur mit minimal 1200°C, was auf ein Hochtemperatur-Ereignis in einer deutlich kühleren Umgebung hinweist. Die späten (pseudosekundäre und sekundäre) CO₂- Fluid-Einschlüsse bilden zwei Generationen von denen die eine in die flüssige (L1), die andere in die Dampfphase (L2) homogenisieren. Die minimale Einschließ-Tiefe für die L1 Generation ist etwa 16 km. Dies bedeutet - auch bei Berücksichtigung der mit diesem Wert verbundenen Ungenauigkeit - daß diese Erdmantel-Gesteine einige Zeit in der mittleren Erdkruste verbrachten und ein metasomatisches Ereignis erlebten, bevor sie von den Basalten zur Erdoberfläche gebracht wurden. Die Tatsache, daß dieses Ereignis die frühen Einschlüsse nicht zerstörte, kann nur bedeuten, daß es von kurzer Dauer war. Die L2-Generation besteht aus Niedrigdruck CO₂-Einschlüssen mit einer Minimum-Einschließtiefe von nur 2 km. Dies könnte in einer seichten Magmakammer des Wirt Basaltes geschehen sein.Die Abfolge von Fluid-Einschlüssen deutet auf einen relativ schnell aufsteigenden oberen Erdmantel unterhalb von Patagonien hin. Die Petrologie und Mineralchemie der peridotitischen Xenolithe unterstützen das. Die Vorherrschaft von Harzburgiten im Erdmantel unterhalb von Nord-Patagonien deutet auf umfangreiche Bildung partieller Schmelzen und deren Abfuhr hin — eine für einen kontinentalen Mantel ungewöhnliche Situation. Sowohl die Verarmungsereignisse, als auch die metasomatischen Veränderungen (einschließlich jene, welche Spuren in Form von Fluid Einschlüssen hinterließen) machen das Vorhandensein eines schnell aufsteigenden Daipirs im oberen Erdmantel dieser Gegend wahrscheinlich. Der Aufstieg kann vom Stabilitätsbereich der Granat-Peridotite bis in die mittlere Kruste verfolgt werden und muß daher relativ schnell erfolgt sein. Unterschiede in Gesteins-, Mineral und Fluid-Eigenschaften zwischen verschiedenen Lokalitäten legen einen diffusen und differenziellen Diapirismus nahe. Zukünftige Studien sollten es ermöglichen, das Gesamtausmaß und die unterschiedlichen Aufstiegshöhen des Diapirs zu kartieren und Hinweise auf seine Entstehung und zukünftige Entwicklung zu erhalten.

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Pyroxene chemistry and evolution of alkali basaltic rocks from Burgenland and Styria,Austria

Summary The mineral chemistry of several Pliocene alkali basaltic rocks from Burgenland and Styria (Eastern Austria) have been investigated in order to determine the evolution path of the basalt magmas prior to eruption. With their wide range of substitutions, clinopyroxenes provide the best records of the evolution history of rocks. Pyroxene phenocrysts of the investigated basalts show both concentric and sector zoning. The investigation of sector zoned crystals shows, that not only Ti, Al and Fe contents are different in different sectors but there can be significant differences also in their Cr content. This fact apparently suggests that the distribution of Cr between clinopyroxene and melt could be influenced by crystallization kinetics.The depth of crystallization and differentiation of the basalts can be estimated from Ti and Al contents of clinopyroxene phenocrysts. From a combination of data on clinopyroxene composition, compatible trace element contents and mg-values of the rocks, it is concluded, that the alkali basalts of Pauliberg and Steinberg underwent slight olivine and clinopyroxene fractionation in shallow magma chambers prior to eruption, while the nephelinite of Stradnerkogel evolved mainly through clinopyroxene fractionation under high pressure conditions, probably in the upper mantle.

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Chemie der Pyroxene und Entwicklung von Alkalibasalten aus dem Burgenland und der Steiermark, Österreich

Zusammenfassung Einige pliozäne alkalibasaltische Gesteine aus dem Burgenland und der Steiermark wurden mineral-chemisch untersucht, um Aufschluß über ihre Evolution vor der Eruption zu erhalten. Klinopyroxene mit ihren vielfältigen Subtitutionsmöglichkeiten erlauben am besten eine Abschätzung der Evolution der Basalte. Pyroxen-Einsprenglinge der Basalte zeigen sowohl konzentrischen als auch sektoralen Zonarbau. Die von uns untersuchten Einsprenglinge zeigen in den verschiedenen Sektoren nicht nur unterschiedliche Gehalte an Ti, Al und Fe, sondern vielfach auch unterschiedliche Cr-Gehalte. Dies macht es wahrscheinlich, daß die Verteilung von Cr zwischen Klinopyroxen und Schmelze von der Kristallisations-Kinetik beeinflußt wird.Die Tiefe in der die Basalte kristallisierten und differenzierten kann von den Ti- und Al-Gehalten der Klinopyroxen- Einsprenglinge abgeschätzt werden. Die Zusammensetzung der Klinopyroxene im Verein mit den Gehalten an kompatiblen Spurenelementen und denmg-Werten der Gesteine erlauben den Schluß, daß die Alkalibasalte von Pauliberg und Steinberg vor ihrer Eruption eine geringfügige Olivinund Klinopyroxen-Fraktionierung in einer seichten Magmakammer erlebten. Der Nephelinit vorn Stradnerkogel hingegen erfuhr hauptsächlich eine Klinopyroxen Fraktionierung unter Hochdruck-Bedingungen, möglicherweise im oberen Erdmantel.

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A new calcium-aluminate from a refractory inclusion in the Leoville carbonaceous chondrite

The first meteoritic occurrence of CaAl₄O₇ is described from a Ca-Al-rich inclusion (CAI) in the Leoville carbonaceous chondrite. This CAI consists mainly of gehlenitic melilite, spinel, perovskite, and hibonite. CaAl₄O₇ is a minor component and occurs within melilite preferentially in portions rich in perovskite.The CAI is enveloped by a succession of three rims (from inside out): (a) hibonite+melilite+spinel+perovskite, (b) diopside, and (c) olivine.On the basis of mineral associations found and from the presence of moderately volatile elements (Fe and Cr) we conclude that the CaAl₄O₇-bearing CAI from Leoville is of residual nature. CaAl₄O₇ is apparently stable in the very Mg- and Si-poor environment of this CAI and is probably of igneous origin.The rims are interpreted as products of partial evaporation (rim (a)) and associated re-condensation (rims (b) and (c)).     

Chemical composition of lunar meteorites and the lunar crust

The paper presents the first analyses of major and trace elements in 19 lunar meteorites newly found in Oman. These and literature data were used to assay the composition of highland, mare, and transitional (highland-mare interface) regions of the lunar surface. The databank used in the research comprises data on 44 meteorites weighing 11 kg in total, which likely represent 26 individual falls. Our data demonstrate that the lunar highland crust should be richer in Ca and Al but poorer in mafic and incompatible elements than it was thought based on studying lunar samples and the first orbital data. The Ir concentration in the highland crust and the analysis of lunar crater population suggest that most lunar impactites were formed by a single major impact event, which predetermined the geochemical characteristics of these rocks. Lunar mare regions should be dominated by low-Ti basalts, which are, however, enriched in LREEs compared to those sampled by lunar missions. The typical material of mare-highland interface zones can contain KREEP and magnesian VLT basalts. The composition of the lunar highland crust deduced from the chemistry of lunar meteorites does not contradict the model of the lunar magma ocean, but the average composition of lunar mare meteorites is inconsistent with this concept and suggests assimilation of KREEP material by basaltic magmas. The newly obtained evaluations of the composition of the highland crust confirm that the Moon can be enriched in refractory elements and depleted in volatile and siderophile elements.     

Foreign meteoritic material of howardites and polymict eucrites

Howardites and polymict eucrites are fragments of regolith breccias ejected from the surface of a differentiated (eucritic) parent body, perhaps, of the asteroid Vesta. The first data are presented demonstrating that howardites contain, along with foreign fragments of carbonaceous chondrites, also fragments of ordinary chondrites, enstatite meteorites, ureilites, and mesosiderites. The proportions of these types of foreign meteoritic fragments in howardites and polymict eucrites are the same as in the population of cosmic dust particles obtained from Antarctic and Greenland ice. The concentrations of siderophile elements in howardites and polymict eucrites are not correlated with the contents of foreign meteoritic particles. It is reasonable to believe that cosmogenic siderophile elements are concentrated in howardites and polymict eucrites mostly in submicrometer-sized particles that cannot be examined mineralogically. The analysis of the crater population of the asteroid Vesta indicates that the flux of chondritic material to the surface of this asteroid should have been three orders of magnitude higher than the modern meteoritic flux and have been comparable with the flux to the moon’s surface during its intense meteoritic bombardment. This provides support for the earlier idea about a higher meteoritic activity in the solar system as a whole at approximately 4 Ga. The lithification of the regolith (into regolith breccia) of the asteroid Vesta occurred then under the effect of thermal metamorphism in the blanket of crater ejecta. Thus, meteorite fragments included in howardites provide record of the qualitative composition of the ancient meteorite flux, which was analogous to that of the modern flux at the Earth surface.     

Lithic fragments,glasses and chondrules from Luna 16 fines

Bulk compositions of igneous and microbreccia lithic fragments, glasses, and chondrules from Luna 16 fines as well as compositions of minerals in basaltic lithic fragments were determined with the electron microprobe. Igneous lithic fragments and glasses are divided into two groups, the anorthositic-noritic-troctolitic (hereafter referred to as ANT) and basaltic groups. Chondrules are always of ANT composition and microbreccia lithic fragments are divided into groups 1 and 2. The conclusions reached may be summarized as follows: (1) Luna 16 fines are more similar in composition to Apollo 11 than to Apollo 12 and 14 materials (e.g. Apollo 11 igneous lithic fragments and glasses fall into similar ANT and basaltic groups; abundant norites in Luna 16 and Apollo 11 are not KREEP as in Apollo 12 and 14; Luna 16 basaltic lithic fragments may represent high-K and low-K suites as is the case for Apollo 11; rare colorless to greenish, FeO-rich and TiO₂-poor glasses were found in both Apollo 11 and Luna 16; Luna 16 spinels are similar to Apollo 11 spinels but unlike those from Apollo 12). (2) No difference was noted in the composition of lithic fragments, glasses and chondrules from Luna 16 core tube layers A and D. (3) Microbreccia lithic fragments of group 1 originated locally by mixing of high proportions of basaltic with small proportions of ANT materials. (4) Glasses are the compositional analogs to the lithic fragments and not to the microbreccias; most glasses were produced directly from igneous rocks. (5) Glasses show partial loss of Na and K due to vaporization in the vitrification process. (6) Luna 16 chondrules have ANT but not basaltic composition. It is suggested that either liquid droplets of ANT composition are more apt to nucleate from the supercooled state; or basaltic droplets have largely been formed in small and ANT droplets in large impact events (in the latter case, probability for homogeneous and inhomogeneous nucleation is larger. (7) No evidence for ferric iron and water-bearing minerals was found. (8) Occurrence of a great variety of igneous rocks in Luna 16 samples (anorthosite, noritic anorthosite, anorthositic norite, olivine norite, troctolite, and basalt) confirm our earlier conclusion that large-scale melting or partial melting to considerable depth and extensive igneous differentiation must have occurred on the moon.     

Depleted lithosphere from the mantle wedge beneath Tres Lagos, southern Patagonia, Argentina

Anhydrous spinel lherzolite and harzburgite xenoliths from Tres Lagos, situated inboard of the Volcanic Arc Gap (VAG) in southernmost Patagonia, are samples of a depleted lithospheric mantle and can be divided into two major groups: metasomatized and non-metasomatized. Metasomatized samples, which are the minority, are partly mylonitized and their metasomatism is related to this tectonic process. A group of non-metasomatized samples have enriched whole rock LREE-abundances that are not consistent with the depleted LREE-abundances in their clinopyroxenes. Intergranular host basalt infiltration could be responsible for the whole rock LREE enrichments. Their Sr- and Nd-isotopic ratios have also been affected by host basalt infiltration, whereas their high Sr-isotopic ratios point to subsequent contamination by ground-water and/or Ca-rich surface solutions. Similar contamination is thought to cause the decoupling of Sr- and Nd-isotopes (high Sr- and Nd-isotopic ratios) observed in the non-metasomatized samples with depleted whole rock LREE. A two-stage partial melting process could be responsible for the origin of the Tres Lagos xenoliths. Model calculations have shown that in the first stage, 2% of batch melting took place in the garnet peridotite field and subsequently the residue experienced 2–8% batch melting in the spinel peridotite field. The Tres Lagos peridotites have not been affected by subduction-related metasomatic processes and they could represent an old lithospheric mantle.     

Petrology of some lithic fragments of alkalic high-alumina basalt composition from Apollo 12 coarse fines

Summary The mineralogy and petrology of three lithic fragments of alkalic highalumina basalt (Kreep) composition from the Apollo 12 coarse fines was studied in detail, using an electron microprobe, in order to gain insight into their crystallization histories. Most rocks of this composition are brecciated and our study indicates that a variety of environments of crystallization can be distinguished for mineral fragments and matrices. Mineral fragments are derived from members of the ANT suite (probably troctolites) in fragments 2 and 5, and the alkalic high-alumina basalt suite in fragment 3. The rocks from which they were derived were coarse-grained, recrystallized and equilibrated, as indicated by major, and especially, minor elements. Minor elements in plagioclase, olivine, pyroxene, and zircon are consistently lower in mineral fragments as compared with matrix minerals. The origin of large zircon fragments is problematic but they are probably from the alkalic high-alumina basalt suite. Mineral fragments may have been derived from plutonic rocks (none have yet been recognized from the alkalic high-alumina basalt suite), but possibly also from breccia fragments which were recrystallized in hot, thick ejecta blankets. The matrix of the lithic fragments is of alkalic high-alumina basalt composition and is either igneous or metamorphic, or both. Hence, lithic fragments 2 and 5 are polymict breccias whereas fragment 3 is a monomict breccia. Matrix glasses in fragments 2 and 3 represent melts fractionated along the orthopyroxeneplagioclase cotectic in the olivine-anorthite-silica pseudoternary system. If these liquids could be separated from the residuum and crystallized they would be, as yet, unrecognized members of the alkalic high-alumina basalt suite. The alkalic high-alumina basalt mixing component of fragment 5 (a polymict breccia) has such a composition and may be derived from such a fractionated rock. A mineral fragment of pyroxene intergrown with ilmenite, approximately parallel to (001), is interpreted as decorated shock lamellae rather than as a deep-seated intergrowth, as found in kimberlites. A glass coating on one side of fragment 3 has SiO₂-rich and feldspathic schlieren and appears to be derived, by impact melting, from a rock of granite composition.

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Petrologie einiger Gesteinsfragmente mit alkalic high-alumina basalt Chemismus aus dem Grobanteil von Apollo 12 Bodenproben

Zusammenfassung Drei Gesteinsfragmente mit alkalic high-alumina basalt (Kreep) Chemismus aus der Grobraktion von Apollo 12 Bodenproben wurden mittels einer Elektronenstrahl-Mikrosonde einer detaillierten Studie unterzogen, um Einblick in ihre Genese zu gewinnen. Der überwiegende Teil von Gesteinen dieser Zusammensetzung ist brekziös und unsere Studie zeigt, daß unterschiedliche Kristallisationsbedingungen für die Mineralfragmente und Matrizes herrschten. Die Mineralfragmente in den Fragmenten 2 und 5 stammen von Gesteinen der ANT- (Anorthositisch-Noritisch-Troctolitischen) Reihe (wahrscheinlich von Troctoliten) und in Fragment 3 von Gesteinen der alkalic high-alumina basalt-Reihe.Die Verteilung der Haupt- und Nebenelemente in den Mineralfragmenten zeigt, daß diese von rekristallisierten und equilibrierten, grobkörnigen Gesteinen stammen. Die Konzentrationen der Nebenelemente sind in allen Mineralfragmenten (Plagioklas, Olivin und Zirkon) deutlich geringer als in den Mineralen der Matrix. Die Herkunft der großen Zirkon-Fragmente ist nicht genau zu klären. Sie stammen jedoch wahrscheinlich von Gesteinen der alkalic high-alumina basalt-Reihe. Alle Mineralfragmente könnten von plutonischen Gesteinen stammen (solche sind von der alkalic highalumina basalt-Reihe zur Zeit noch nicht bekannt), sie könnten ihren Ursprung jedoch auch in prä-existenten Brekzien haben, welche in dichten, heißen Auswurfdecken rekristallisierten. Die Matrix der Gesteinsfragmente hat durchwegs eine alkalic high-alumina basalt Zusammensetzung und ist entweder magmatisch oder metamorph, oder beides. Die Fragmente 2 und 5 sind daher als polymikte und das Fragment 3 als monomikte Brekzie zu bezeichnen.Die Matrixgläser in den fragmenten 2 und 3 repräsentieren Rest-schmelzen, welche entlang der Orthopyroxen-Plagioklas-Kotektik im Olivin-Anorthit-SiO₂-System fraktionierten. Diese Schmelzen würden-könnten sie vom System getrennt werden-bisher noch nicht bekannte Glieder der alkalic high-alumina basalt-Reihe darstellen. Eine derartige Zusammensetzung hat jedoch die Mischkomponente im Fragment 5 (eine polymikte Brekzie), welche von einem auf diesem Wege fraktioniertem Gestein stammen könnte.Ilmenit-Lamellen [subparallel zu (001)] in einem Pyroxenfragment stellen eher dekorierte Schocklamellen als Verwachsungen, wie sie aus Kimberliten bekannt sind, dar. Fragment 3 ist einseitig mit einem schlierigen Glas bedeckt, dessen Schlieren angenähert die Zusammensetzung von Alkalifeldspat und reinem SiO₂ haben. Dieses Glas ist offensichtlich eine Impakt-Schmelze eines Gesteines von granitischer Zusammensetzung.

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The non‐igneous genesis of angrites: Support from trace element distribution between phases in D'Orbigny

Abstract— D'Orbigny is an exceptional angrite. Chemically, it resembles other angrites such as Asuka‐881371, Sahara 99555, Lewis Cliff (LEW) 87051, and LEW 86010, but its structure and texture are peculiar. It has a compact and porous lithology, abundant glasses, augite‐bearing druses, and chemical and mineralogical properties that are highly unusual for igneous rocks. Our previous studies led us to a new view on angrites: they can possibly be considered as CAIs that grew to larger sizes than the ones we know from carbonaceous chondrites. Thus, angrites may bear a record of rare and special conditions in some part of the early solar nebula. Here we report trace element contents of D'Orbigny phases. Trace element data were obtained from both the porous and the compact part of this meteorite. We have confronted our results with the popular igneous genetic model. According to this model, if all phases of D'Orbigny crystallized from the same system, as an igneous origin implies, a record of this genesis should be expressed in the distribution of trace elements among early and late phases. Our results show that the trace element distribution of the two contemporaneous phases olivine and plagioclase, which form the backbone of the rock, seem to require liquids of different composition. Abundances of highly incompatible elements in all olivines, including the megacrysts, indicate disequilibrium with the bulk rock and suggest liquids very rich in these elements (>10,000 x CI), which is much richer than any fractional crystallization could possibly produce. In addition, trace element contents of late phases are incompatible with formation from the bulk system's residual melt. These results add additional severe constraints to the many conflicts that existed previously between an igneous model for the origin of angrites and the mineralogical and chemical observations. This new trace element content data, reported here, corroborate our previous results based on the shape, structure, mineralogy, chemical, and isotopic data of the whole meteorite, as well as on a petrographic and chemical composition study of all types of glasses and give strength to a new genetic model that postulates that D'Orbigny (and possibly all angrites) could have formed in the solar nebula under changing redox conditions, more akin to chondritic constituents (e.g., CAIs) than to planetary differentiated rock.