Magmatic inclusions in rhyolites,contaminated basalts,and compositional zonation beneath the Coso volcanic field,California

Basaltic lava flows and high-silica rhyolite domes form the Pleistocene part of the Coso volcanic field in southeastern California. The distribution of vents maps the areal zonation inferred for the upper parts of the Coso magmatic system. Subalkalic basalts (<50% SiO₂) were erupted well away from the rhyolite field at any given time. Compositional variation among these basalts can be ascribed to crystal fractionation. Erupted volumes of these basalts decrease with increasing differentiation. Mafic lavas containing up to 58% SiO₂, erupted adjacent to the rhyolite field, formed by mixing of basaltic and silicic magma. Basaltic magma interacted with crustal rocks to form other SiO₂-rich mafic lavas erupted near the Sierra Nevada fault zone.Several rhyolite domes in the Coso volcanic field contain sparse andesitic inclusions (55–61% SiO₂). Pillow-like forms, intricate commingling and local diffusive mixing of andesite and rhyolite at contacts, concentric vesicle distribution, and crystal morphologies indicative of undercooling show that inclusions were incorporated in their rhyolitic hosts as blobs of magma. Inclusions were probably dispersed throughout small volumes of rhyolitic magma by convective (mechanical) mixing. Inclusion magma was formed by mixing (hybridization) at the interface between basaltic and rhyolitic magmas that coexisted in vertically zoned igneous systems. Relict phenocrysts and the bulk compositions of inclusions suggest that silicic endmembers were less differentiated than erupted high-silica rhyolite. Changes in inferred endmembers of magma mixtures with time suggest that the steepness of chemical gradients near the silicic/mafic interface in the zoned reservoir may have decreased as the system matured, although a high-silica rhyolitic cap persisted.The Coso example is an extreme case of large thermal and compositional contrast between inclusion and host magmas; lesser differences between intermediate composition magmas and inclusions lead to undercooling phenomena that suggest smaller T. Vertical compositional zonation in magma chambers has been documented through study of products of voluminous pyroclastic eruptions. Magmatic inclusions in volcanic rocks provide evidence for compositional zonation and mixing processes in igneous systems when only lava is erupted.     

Subsource characterization: Obsidian utilization of subsources of the Coso volcanic field,Coso Junction,California, USA

Six chemical subsource groups were identified in the analysis of 84 obsidian samples collected from subsource locations at Coso volcanic field, California. In prehistoric times, Coso provided obsidian for artifacts found from San Francisco Bay to San Diego to Death Valley to the eastern Mojave Desert. Subsource groups were defined by instrumental neutron activation analysis (INAA) of 29 elements followed by cluster analysis, principal component analysis, and bivariate plotting. The new data are compared to previously published INAA and X‐ray fluorescence data. Characterization of 55 obsidian artifacts from archaeological sites located approximately 100 miles from Coso suggests preferential usage of specific subsources as a function of the directionality of travel. The results are consistent with a bimodal (resident and itinerant) model of procurement. This research illustrates the importance of accurate sourcing of obsidian artifacts when attempting to define subsource usage. © 2004 Wiley Periodicals, Inc.     

Melting in the lithospheric mantle: Inverse modelling of alkali-olivine basalts from the Big Pine Volcanic Field,California

The variations in trace element abundances of a suite of alkali-olivine basalts from the Big Pine volcanic field, California, have been ‘inverted’ following the method of Hofmann and co-workers to obtain source concentration and distribution coefficient data. The high Mg-numbers and ne-normative mineralogy of these lavas allow a simple correction to be made for fractional crystallisation, and together with a limited range in ⁸⁷Sr/⁸⁶Sr (0.7056–0.7064), suggest derivation from a relatively homogeneous source region. Negative correlations between SiO₂ and P₂O₅, and SiO₂ and Rb in the calculated primary magmas imply that both major and trace elements vary in a coherent fashion as a function of the degree of partial melting. The Big Pine lavas are characterised by high ratios of large-ion lithophile to high-field strength elements (Ba/Nb>60), and the inverse procedure demonstrates that this reflects source concentrations, as opposed to a mineralogical control. The calculated mantle source is further characterised by generally high abundances of Sr, Ba, K, and Th relative to Nb and Ta which imply that incompatible element enrichment of the source occurred above a subduction zone. A model Sm/Nd age of 1.8 Ga for this enrichment coincides with the regional crustal formation age. Such features imply that both the major and trace element components of the Big Pine lavas are derived from within lithospheric mantle, perhaps mobilised by the high geothermal gradients which characterise the extensional environment of the Basin and Range Province. A comparison with other Cenozoic mafic lavas throughout the western United States suggests that a substantial proportion of the mantle lithosphere in this area has similar chemical characteristics to the source of the Big Pine lavas. If this is the case, then it implies that convergent margins represent an important tectonic environment for the formation of lithospheric mantle.     

Rhyolite Thermobarometry and the Shallowing of the Magma Reservoir, Coso Volcanic Field, California

The compositionally bimodal Pleistocene Coso volcanic fieldis located at the western margin of the Basin and Range province     

Clinopyroxene zoning patterns in the young alkali basalts of Hungary and their petrogenetic significance

In the Upper Pliocene, during the final phase of igneous activity within the Pannonian Basin, alkali basalts were erupted. Their occurrences are restricted to two main regions in Hungary: 1) Transdanubia; 2) Nógrád County. The clinopyroxene phenocrysts of these rocks are zoned titanaugites which often have distinctive colourless or green cores. Two kinds of green cores can be distinguished: 1. olive-green cores (fassaitic augite and fassaite), and 2. grassgreen cores (salite and ferrosalite). Both types of green cores are comparatively iron-rich and they occur only in the basalts of Nógrád County. The olive-green fassaites probably precipitated from relatively evolved melts which have been mixed into their present host magmas, whereas the grassgreen salites and ferrosalites are xenocrysts derived probably from upper mantle rocks. The clinopyroxene zoning patterns suggest, that after being generated by small-degree partial melting in the mantle the Transdanubian basalts ascended to the surface with little or no modification en route, whereas those of Nógrád County had a more complex evolution, in which fractionation at depth and magma mixing played an important role.     

Lead and strontium isotopic evidence for crustal interaction and compositional zonation in the source regions of Pleistocene basaltic and rhyolitic magmas of the Coso volcanic field,California

The isotopic compositions of Pb and Sr in Pleistocene basalt, high-silica rhyolite, and andesitic inclusions in rhyolite of the Coso volcanic field indicate that these rocks were derived from different levels of compositionally zoned magmatic systems. The 2 earliest rhyolites probably were tapped from short-lived silicic reservoirs, in contrast to the other 36 rhyolite domes and lava flows which the isotopic data suggest may have been leaked from the top of a single, long-lived magmatic system. Most Coso basalts show isotopic, geochemical, and mineralogic evidence of interaction with crustal rocks, but one analyzed flow has isotopic ratios that may represent mantle values (⁸⁷Sr/⁸⁶Sr=0.7036,²⁰⁶Pb/²⁰⁴Pb=19.05,²⁰⁷Pb/²⁰⁴Pb=15.62,²⁰⁸Pb/²⁰⁴Pb= 38.63). The (initial) isotopic composition of typical rhyolite (⁸⁷Sr/⁸⁶Sr=0.7053,²⁰⁶Pb/²⁰⁴Pb=19.29,²⁰⁷Pb/²⁰⁴Pb= 15.68,²⁰⁸Pb/²⁰⁴Pb=39.00) is representative of the middle or upper crust. Andesitic inclusions in the rhyolites are evidently samples of hybrid magmas from the silicic/mafic interface in vertically zoned magma reservoirs. Silicic end-member compositions inferred for these mixed magmas, however, are not those of erupted rhyolite but reflect the zonation within the silicic part of the magma reservoir. The compositional contrast at the interface between mafic and silicic parts of these systems apparently was greater for the earlier, smaller reservoirs.     

Textural evolution and metamorphism of pillow basalts from the Franciscan Complex,western Marin County,California

Petrogenesis of Franciscan pillow basalts from the Franciscan Complex of western Marin County California entails both dynamic crystallization of tholeiitic magma and subsequent low-temperature metamorphism. Brittle deformation during tectonic emplacement of pillow basalts into a chert greywacke terrain is manifested by the shearing of interpillow matrix and polishing of pillow rims, but the igneous textures within pillows are well preserved.The cooling history of pillow basalts can be understood through analysis of morphologic variations of primary olivine and plagioclase from rim to core of the pillow. Crystal sizes and plagioclase dendrite spacings are consisted with a cooling rate which generally decreases inward. Some pillows show a marked asymmetry in plagioclase and olivine morphology suggesting lower cooling rates caused by asymmetric cooling of the pillows. Olivine morphologies, primarily hopper and chain forms, are consistent with cooling rates of 2–10 °C/h for pillow cores and 50–75 °C/h for pillow rims.Low temperature hydrothermal alteration has produced secondary minerals indicative of zeolite facies conditions. Pillow matrix is either chloritic or zeolitic (in part laumontized). Pillow rims display incomplete replacement of calcic palagonite by pumpellyite (Fe₂O₃=9–21 wt%), prehnite (Fe₂O₃=5–7 wt%), sphene and quartz. Metamorphism of pillow interiors, manifested by: (1) veins of quartz, pumpellyite, calcite, or harmotome (BaO=15 wt%); (2) amygdules containing analcime, chlorite or quartz; and (3) replacement of olivine by pumpellyite or smectite/illite, of plagioclase by albite (An3)+sericite, and of glassy groundmass by fine-grained chlorite. Primary augite (Wo3₃₉En₁₃Fs₄₈) was not altered. The described paragenesis may be attributed to oceanfloor and/or Franciscan-type metamorphism.     

Residence, Resorption and Recycling of Zircons in Devils Kitchen Rhyolite, Coso Volcanic Field, California

Zircons from the Devils Kitchen rhyolite in the PleistoceneCoso Volcanic field, California have been analyzed by in situPb/U ion microprobe (SHRIMP-RG) and by detailed cathodoluminescenceimaging. The zircons yield common-Pb-corrected and disequilibrium-corrected²⁰⁶Pb/²³⁸U ages that predate a previously reported K–Arsanidine age by up to 200 kyr, and the range of ages exhibitedby the zircons is also approximately 200 kyr. Cathodoluminescenceimaging indicates that zircons formed in contrasting environments.Most zircons are euhedral, and a majority of the zircons areweakly zoned, but many also have anhedral, embayed cores, witheuhedral overgrowths and multiple internal surfaces that aretruncated by later crystal zones. Concentrations of U and Thvary by two orders of magnitude within the zircon population,and by 10–20 times between zones within some zircon crystals,indicating that zircons were transferred between contrastingchemical environments. A zircon saturation temperature of 750°Coverlaps within error a previously reported phenocryst equilibrationtemperature of 740 ± 25°C. Textures in zircons indicativeof repeated dissolution and subsequent regrowth are probablycaused by punctuated heating by mafic magma input into rhyolite.The overall span of ages and large variation in U and Th concentrations,combined with calculated zircon saturation temperatures andresorption times, are most compatible with crystallization inmagma bodies that were emplaced piecemeal in the crust at Cosoover 200 kyr prior to eruption, and that were periodically rejuvenatedor melted by subsequent basaltic injections. KEY WORDS: zircon geochronology; residence time; rhyolite; ion microprobe; California     

Clinopyroxene chemistry in Tertiary alkaline volcanic rocks from Taleghan,central Alborz,Iran: Implications for two parental melts

In the Taleghan area of Alborz mountain range, two distinct units of alkaline rocks are identified. Whole rock major and trace element data does not provide a clue as to their common or different parental melts. However, major and trace element geochemistry of their included clinopyroxene phenocrysts, combined with the whole rock data, helped to infer that two parental magmas were involved in the evolution of volcanic succession in the Taleghan area.     

Geochemical modelling of basalts from DSDP Leg 65, East Pacific Rise,Gulf of California

Major and rare earth element (REE) data for basalts from Holes 483, 483B, and 485A of DSDP Leg 65, East Pacific Rise, mouth of the Gulf of California, support a simple fractional crystallization model for the genesis of rocks from this suite. The petrography and mineral chemistry (presented in detail elsewhere) provide no evidence for magma mixing, but rather a simple multistage cooling process. Based on its lowest TiO₂ content (0.88%), $\text{FeO}{}^1\text{MgO}$ ratio (0.95 with total Fe as FeO), and Mg# (100 $\text{Mg}\text{Mg + Fe}\text{″ = 70}$), sample 483-17-2-(78–83) has been selected as the most primitive primary magma of the samples analyzed. This is supported by the REE data which show this sample has the lowest total REE content, a $\text{La}\text{Sm}{}_{\mathrm{cn}}$ (chondrite-normalized) = 0.36, and $\text{Eu}\text{Sm}{}_{\mathrm{cn}}$ = 1.05. Because other samples analyzed have higher SiO₂, lower Mg#, and a negative Eu anomaly ($\text{Eu}\text{Sm}{}_{\mathrm{cn}}$ as low as 0.89), they are most likely derivative magmas. Wright-Doherty and trace element modelling support fractional crystallization of 14.1% plagioclase (An₈₈), 6.7% olivine (Fo₈₆), and 4.7% clinopyroxene (Wo₄₁En₄₉Fs₁₀) from 483-17-2-(78–83) to form the least differentiated sample with Mg# = 63. The $\text{La}\text{Sm}{}_{\mathrm{cn}}$ of this derivative magma is almost identical to the parent magma (0.35 to 0.36), but the other samples have higher $\text{La}\text{Sm}{}_{\mathrm{cn}}$ (0.45 to 0.51), more total REE, and lower Mg# (60 to 56). Both Wright-Doherty and trace element modelling indicate that the primary magma chosen cannot produce these more evolved samples. For the major elements, the TiO₂ and P₂O₅ are too low in the calculated versus the observed (1.38 to 1.90; 0.11 to 0.17, respectively, for example). Rayleigh fractionation calculates a lower $\text{La}\text{Sm}{}_{\mathrm{cn}}$ and requires about 60% crystal removal versus 40% for the Wright-Doherty. These more evolved samples must be derived from a parent magma different from the one selected here and, unfortunately, not sampled in this study. A magma formed by a smaller degree of partial melting with slightly more residual clinopyroxene left in the mantle than for sample 483-17-2-(78–83) is required.     

High pressure phase relations of primitive high-alumina basalts from Medicine Lake volcano,northern California

Anhydrous phase relations were determined at 1 atm and 10 to 15 kbar for primitive high-alumina basalts (79–35g and 82–72f) from Giant Crater at Medicine Lake volcano. These compositions are multiply saturated with olivine+augite+plagioclase+spinel+/-orthopyroxene near the liquidus at about 11 kbar. Experiments on mixtures of sample 79–35g with orthopyroxene and olivine determined the location of the multiple saturation boundaries where liquid coexists with the assemblage olivine+augite+orthopyroxene+plagioclase at 10 kbar and olivine+augite+orthopyroxene+spinel at 15 kbar. The mix experiments showed that primitive Medicine Lake high alumina basalts (HABs) are close in composition to liquids in equilibrium with a mantle lherzolite source containing olivine+augite+ orthopyroxene+spinel+plagioclase at 11 kbar. Orthopyroxene observed as a near liquidus phase in an 11 kbar experiment on sample 82–72f supports this conclusion. The most primitive HABs from Medicine Lake are low in K₂O (0.07 wt.%), high in MgO (>10 wt.%) and Ni (231 ppm), and have light-rare earth element depletions and large ion lithophile element enrichments. A model for the origin of these near-primary high-alumina basalts is that they are partial melts of a MORB-like mantle lherzolite source that has been enriched by a fluid component derived from the subducted slab. The HAB magma segregated from its mantle residue just below the base of the crust near the crust-mantle boundary.     

Crustal contamination and mantle source characteristics in continental intra-plate volcanic rocks: Pb, Hf and Os isotopes from central European volcanic province basalts

We report new Os-Pb-Hf isotope data for a suite of alkaline to basaltic (nephelinites, basanites, olivine tholeiites to quartz-tholeiites) lavas from the Miocene Vogelsberg (Germany), the largest of the rift-related continental volcanic complexes of the Central European Volcanic Province (CEVP). ¹⁸⁷Os/¹⁸⁸Os in primitive (high-MgO) alkaline lavas show a much wider range than has been observed in alkaline basalts and peridotite xenoliths from elsewhere in the CEVP, from ratios similar to those in modern MORB and OIB (0.1260-0.1451; 58.9-168 ppt Os) to more radiogenic ratios (0.1908 and 0.2197; 27.6-15.1 ppt Os). Radiogenic Os is associated with high ε_Hf and ε_Nd, low ⁸⁷Sr/⁸⁶Sr and does not correlate with Mg^∗ or incompatible trace elements (e.g. Ce/Pb), suggesting the presence of a radiogenic endmember in the mantle rather than crustal contamination as the source of radiogenic Os. This contrasts with another high-Mg alkaline lava characterized by highly radiogenic ¹⁸⁷Os/¹⁸⁸Os (0.4344, 10.3 ppt Os), lower ε_Hf and ε_Nd, higher ⁸⁷Sr/⁸⁶Sr, and Pb isotope signatures than the other alkaline lavas with similar trace element composition suggestive of contamination with crustal material. Hafnium (ε_Hf: +8.9 to +5.0) and Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb: 19.10-19.61; ²⁰⁷Pb/²⁰⁴Pb: 15.56-15.60) of the alkaline rocks fall within the range of enriched MORB and some OIB. The Vogelsberg tholeiites show even more diverse ¹⁸⁷Os/¹⁸⁸Os, ranging from 0.1487 in Os-rich olivine tholeiite (31.7 ppt) to ratios as high as 0.7526 in other olivine-tholeiites and in quartz-tholeiites with lower Os concentrations (10.3-2.0 ppt). Low-¹⁸⁷Os/¹⁸⁸Os tholeiites show Pb-Hf isotope ratios (²⁰⁶Pb/²⁰⁴Pb:18.81; ²⁰⁷Pb/²⁰⁴Pb: 15.61; ε_Hf: +2.7) that are distinct from those in alkaline lavas with similar ¹⁸⁷Os/¹⁸⁸Os and originate from a different mantle source. By contrast, the combination of radiogenic Os and low ²⁰⁶Pb/²⁰⁴Pb and ε_Hf in the other tholeiites probably reflects crustal contamination.The association at Vogelsberg of primitive alkaline and tholeiitic lavas with a range of MORB- to OIB-like Os-Pb-Hf-Nd-Sr isotopic characteristics requires at least two asthenospheric magma sources. This is consistent with trace element modelling which suggests that the alkaline and tholeiitic parent magmas represent mixtures of melts from garnet and spinel peridotite sources (both with amphibole), implying an origin of the magmas in the garnet peridotite-spinel peridotite transition zone, probably at the asthenosphere-lithosphere interface. We propose that uncontaminated Vogelsberg lavas originated in ‘metasomatized’ mantle, involving a 3-stage model: (1) early carbonatite metasomatism several 10-100 Ma before the melting event (2) deposition of low-degree asthenospheric melts from carbonated peridotite at the lithosphere-asthenosphere thermal boundary produces hydrous amphibole-bearing veins or patches, and (3) remobilization of this modified lithospheric mantle into other asthenospheric melts passing through the same area later. In keeping with ‘metasomatized’ mantle models for other continental basalt provinces, we envisage that stage (2) is short-lived (few Ma), thus producing a prominent lithospheric trace element signature without changing the asthenospheric isotopic signatures. Models of this type can explain the peculiar mix of lithospheric (prominent depletions of Rb and K) and asthenospheric (OIB-like high ¹⁸⁷Os/¹⁸⁸Os, ¹⁴³Nd/¹⁴⁴Nd and ¹⁷⁶Hf/¹⁷⁷Hf) signatures observed in the Vogelsberg and many other continental basalt suites.     

Prograde and retrograde history of the Junction School eclogite,California, and an evaluation of garnet–phengite–clinopyroxene thermobarometry

Quantitative thermobarometry of inclusions in zoned garnet from a Franciscan eclogite block record a counter-clockwise P–T path from blueschist to eclogite and back. Garnet retains prograde zoning from inclusion-rich Alm₅₂Grs₃₀Pyp₆Sps₁₂ cores to inclusion-poor Alm₆₂Grs₂₅Pyp₁₂Sps₁ mantles, with overgrowths of highly variable composition. Barometry using the Waters–Martin version of the garnet–phengite–omphacite thermobarometer yields conditions of 7–15 kbar, 400–500°C (garnet cores), 18–22 kbar, ∼550°C (mantles), and 10–14 kbar, 350–450°C (overgrowths), in agreement with clinozoisite–sphene–rutile–garnet–quartz barometry. These pressures are ∼10–15 kbar less than those obtained using more recent, fully thermodynamic calibrations of the phengite–omphacite–garnet thermobarometer. Low early temperatures suggest that the block was subducted in a thermally mature subduction zone and not at the inception of subduction when prograde temperature is expected to be higher. Franciscan high-grade blocks likely represent crust subducted throughout the history of this convergent margin, rather than only at the inception of the subduction zone.     

Qualitative thermobarometry of inverted metamorphism in the Pelona and Rand Schists, southern California, using calciferous amphibole in mafic schist

Abstract The Rand and Pelona Schists consist of eugeoclinal rock types overlain by continental basement along the Vincent-Chocolate Mountains (VCM) faults. Both schists display inverted metamorphic zonation, defined in part by a systematic variation in composition of calcic to sodic-calcic amphibole in mafic schist structurally upward. The compositional progressions include increase of total A1, A1^IV and Ti, but decrease in the ratios of Na/(Na + Ca) to A1/(A1 + Si), and Na^M4 to (A1^VI+ Fe³⁺+ Ti). These variations imply that structurally high rocks belong to a lower-pressure metamorphic fades series than those at depth. This result is consistent with previous views that the inverted metamorphic zonations represent intact structural sequences.
Amphibole composition is dependent not only on structural position (i.e. P-T ), but also upon bulk-rock composition. The important controls are whole-rock Mg/(Mg + Fe²⁺+ Mn) and Fe³⁺/Fe²⁺. The greatest impact of these factors, however, is on the absolute values of Na and Al, rather than their ratio. Thus, interpretation of facies series is not seriously hindered by compositional variability.
Sodic amphibole in epidote blueschists from the Rand Schist is extensively replaced by sodic-calcic amphibole. Sodic-calcic amphibole in the Rand Schist and Pelona Schist is, itself, rimmed by actinolitic amphibole. Similar blueschist to greenschist transitions in other metamorphic terranes are typically attributed to exhumation. In the Rand and Pelona Schists, the sequence probably formed during burial.     

Clinopyroxene chemistry of the high-Potassium suite from the Alban Hills,Italy

Summary Chemical data on clinopyroxene phenocrysts in twenty-four lava samples from the Alban Hills (Roman comagmatic region) show coexistence, within the same rock, of two core-rim evolution trends: diopside-salite and salite-diopside, respectively. The Alban volcanics can be divided in two groups depending on which type of core predominates.Geochemical mixing tests, conducted with elements showing a different degree of incompatibility, such as Ce, Sr, Th, La, Ta, and Hf, show no evidence of a mixing process which might be responsible for coexistence of both diopside and salite clinopyroxenes within the same lava.Taking into account the results of known experiments on the influence of water on clinopyroxene composition in potassium rich lavas, the reverse zoning trend observed and the consequent predominance of salite cores in some lavas are ascribed to the effect of volatiles, and particularly to water. Changes of water pressure may also be responsible for phenocryst corrosion and salitic clinopyroxene replacement by olivine, phlogopite and titaniferous magnetite.The prominent role of water in the Alban Hills magma evolution is also supported by the high fluorine content found in the Alban products, which enhances water solubility in the magmas, by the frequent occurrence of mica in the rock groundmass and, finally, by the explosive character of Alban volcanism.

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Zusammenfassung Die Ergebnisse chemischer Analysen von Klinopyroxen in vierundzwanzig Lavaproben aus den Albaner Bergen (Römische Komagmatische Region) zeigen die Koexistenz von zwei Kern-Rand-Entwicklungstendenzen: Diopsid-Salit und Salit-Diopsid. Die Vulkanite können auf Grund der Zusammensetzung der Kerne in zwei Gruppen unterteilt werden.Mit Elementen verschiedener Inkompatibilität, wie Ce, Sr, Th, La, Ta und Hf, ausgeführte Mischversuche geben keinen Hinweis dafür, daß ein Mischungsprozeß für die Koexistenz von Diopsid und Salit in derselben Lava verantwortlich sei.In Anbetracht der Ergebnisse von Experimenten über den Einfluß von H₂O auf die Klinopyroxen-Zusammensetzung in K-reichen Laven, werden die beobachtete Zonierung und die daraus folgende Dominanz von Salit-Kernen in bestimmten Lavatypen der Wirkung von volatilen Bestandteilen, besonders Wasser, zugeschrieben. änderungen des H₂O-Drucks können für Phenokristall-Korrosion und Verdrängung der salitischen Klinopyroxene durch Olivin, Phlogopit und Titanomagnetit verantwortlich sein.Die entscheidende Rolle des Wassers in der Entwicklung des Magmas stimmt mit dem hohen Fluor-Gehalt der Produkte, der die H₂O-Löslichkeit in Magmen erhöht, mit der Häufigkeit des Glimmers in der Grundmasse der Gesteine und mit der explosiven Natur des Vulkanismus im Untersuchungsgebiet überein.

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Zur Chemie der Klinopyroxene in den Kali-reichen Gesteinen der Albaner Berge

     

Potassium basalts and picrobasalts from the devonian kimberlite fields of Western Yakutia, Russia, and their relations to kimberlite magmatism

Basic explosion pipes occur along with basic dikes, sills, and chonoliths within the Vilyui—Markha basic dike belt in the northwestern marginal part of the Vilyui Rift, characterized by widespread basaltic magmatism. The explosion pipes are of interest for exploration geology owing to their specific composition and tectonic setting, similar in many respects to the structural localization of kimberlite bodies in the sedimentary cover of the Siberian Platform. The basic explosion pipes from the Mirny district were referred to as tholeiitic and alkali-basaltic petrochemical rock series. Peculiar potassic and ultrapotassic rocks—potassium olivine basalts and picrobasalts—were identified in the alkali-basaltic series. These rocks were regarded as related to the deepest sources among basalts and were recommended for use as a prospecting guide for primary diamond sources. Our investigations allowed us to interpret the elevated K and Mg contents in basic fragments from some explosion pipes and associated intrusive bodies as a result of low-temperature metasomatic alteration. The explosion breccias and metasomatically altered basic rocks probably mark areas favorable for explosion activity and intrusion of both basic and kimberlitic rocks.     

Complementary trace-element fractionation in volcanic and plutonic rocks: imperfect examples from ocean-floor basalts and gabbros

A simple trace-element model that is generalized from one devised by Albarede (1976) can be used to treat plutonic rocks as mixtures of cumulate phases and trapped liquid. The model is based on the Rayleigh fractionation law, mass balance, and modal data and, with certain assumptions, can give estimates of the mass fraction of the liquid component (X ^l) in a cumulate rock and of some of the characteristics of that liquid, including trace-element concentrations and the mass fraction of the original liquid (F) that remained in the magma chamber when some of it was trapped. Application of the model to Cr and Zr data for ten dredged gabbros from the Oceanographer Fracture Zone (OFZ) in the North Atlantic yields results in the range X ^l=0.014–0.17 and F=0.04–0.22. A more complex model extends the equations developed by Greenland (1970) and combines them with constraints from 1-atm experiments on ocean-floor basalts to effectively map phase-saturation boundaries onto trace-element variation diagrams. On a Zr-Sr plot, the model is capable of mimicking mixing chords and differences in liquid lines of descent (or parental compositions) inferred from major-element chemistry for several OFZ basalts. Qualitatively, the associated gabbros can also be rationalized as cumulate/melt mixtures on this diagram, although the allowable range of liquid compositions is large. In addition, there is some suggestion that the Zr-Sr liquid line of descent fitted to the OFZ basalts may have more general relevance to other ocean-floor rocks (e.g., Galapagos and FAMOUS glasses).     

Chemistry and isotope ratios of sulfur in basalts and volcanic gases at Kilauea volcano,Hawaii

Eighteen basalts and some volcanic gases from the submarine and subaerial parts of Kilauea volcano were analyzed for the concentration and isotope ratios of sulfur. By means of a newly developed technique, sulfide and sulfate sulfur in the basalts were separately but simultaneously determined. The submarine basalt has 700 ± 100 ppm total sulfur with δ³⁴S_Σs of $\text{0.7 ± 0.1 ‰}$. The sulfate/sulfide molar ratio ranges from 0.15 to 0.56 and the fractionation factor between sulfate and sulfide is $\text{+7.5 ± 1.5‰}$. On the other hand, the concentration and δ³⁴S_Σs values of the total sulfur in the subaerial basalt are reduced to 150 ± 50 ppm and $\text{?0.8 ± 0.2‰}$, respectively. The sulfate to sulfide ratio and the fractionation factor between them are also smaller, 0.01 to 0.25 and +3.0‰, respectively. Chemical and isotopic evidence strongly suggests that sulfate and sulfide in the submarine basalt are in chemical and isotopic equilibria with each other at magmatic conditions. Their relative abundance and the isotope fractionation factors may be used to estimate the $\text{?o}{}_2$ and temperature of these basalts at the time of their extrusion onto the sea floor. The observed change in sulfur chemistry and isotopic ratios from the submarine to subaerial basalts can be interpreted as degassing of the SO₂ from basalt thereby depleting sulfate and ³⁴S in basalt.The volcanic sulfur gases, predominantly SO₂, from the 1971 and 1974 fissures in Kilauea Crater have δ³⁴S values of 0.8 to 0.9%., slightly heavier than the total sulfur in the submarine basalts and definitely heavier than the subaerial basalts, in accord with the above model. However, the δ³⁴S value of sulfur gases (largely SO₂) from Sulfur Bank is 8.0%., implying a secondary origin of the sulfur. The δ³⁴S values of native sulfur deposits at various sites of Kilauea and Mauna Loa volcanos, sulfate ions of four deep wells and hydrogen sulfide from a geothermal well along the east rift zone are also reported. The high δ³⁴S values (+5 to +6%._o) found for the hydrogen sulfide might be an indication of hot basaltseawater reaction beneath the east rift zone.     

Metamorphism, geochemistry and origin of magnesian volcanic rocks, Klamath Mountains, California

Metabasaltic rocks in the Klamath Mountains of California with ‘komatiitic’ major element concentrations were investigated in order to elucidate the origin of the magnesian signature. Trace-element concentrations preserve relict igneous trends and suggest that the rocks are not komatitic basalts, but immature arc rocks and within-plate alkalic lavas. Correlation of ‘excess’ MgO with the volume per cent hornblende (±clinopyroxene) suggests that the presence of cumulus phases contributes to the MgO-rich compositions. Early submarine alteration produced regional δ¹⁸O values of +10±1.5%_° and shifts in Al₂O₃, Na₂O, and K₂O concentrations. Regional metamorphic grade in the study area varies from biotite-zone greenschist facies (350–550°C, c. 3 kbar) southward to prehnite–actinolite facies (200–400°C, ≤3 kbar), but little isotopic or elemental change occurred during the regional recrystallization. The greenschist facies assemblage is actinolitic hornblende + phengite + epidote + sodic plagioclase + microcline + chlorite + titanite + hematite + quartz in Ti-poor metabasaltic rocks; in addition to these phases biotite is present in Ti-rich analogues. Lower grade greenstones contain prehnite and more nearly stoichiometric actinolite. The moderate to low pressures of regional metamorphism are compatible with P–T conditions in a magmatic arc. Later contact metamorphism at 2–2.9±0.5 kbar and at peak temperatures approaching 600° C around the English Peak and Russian Peak granodiorites produced 3–4–km-wide aureoles typified by gradual, systematic increases in the pargasite content of amphibole, muscovite content of potassic white mica, and anorthite content of plagioclase compositions. Metasomatism during contact metamorphism produced further increases in bulk-rock δ¹⁸O_SMOW of as much as +6%_°. Thus, the unusually MgO-rich nature of the Sawyers Bar rocks may be attributed at least partly to metasomatism and the presence of magnesian cumulus phases.     

Exceptionally Cr-rich basalts in the komatiitic volcanic association of the Archaean Kuhmo greenstone belt, eastern Finland

Summary Exceptionally Cr-rich metabasalts related to a komatiite-dominant volcanic sequence occur in the Archaean Kuhmo greenstone belt, eastern Finland. These basalts contain more chromium (1300–4500 ppm) than any other terrestrial basalts analysed so far, and also have high nickel concentrations (200–1700 ppm). In stratigraphy, these Cr-rich basalts occur above the komatiite and komatiitic basalt units forming the uppermost units of the komatiite sequence. Extremely reducing conditions during magma generation or fractional crystallization are suggested as a reason for these exceptional compositions. Low oxygen fugacity has prevented crystallization of chromite and decreased the olivine/liquid partition coefficient for nickel in olivine fractionation, thus causing the enrichment of Cr and Ni in the residual melt.

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Zusammenfassung Au?ergew?hnlich Cr-reiche Basalte in der komatiitischen vulkanischen Assoziation des Archaischen Kuhmo-Grünsteingürtels in Ostfinnland Im archaischen Kuhmo-Grünsteingürtel in Ostfinnland treten au?ergew?hnlich Cr-reiche Metabasalte auf, die mit einer komatiitdominanten vulkanischen Sequenz verbunden sind. Diese Basalte enthalten mehr Chrom (1300–4500 ppm) als alle anderen terrestrischen Basalte, die bislang analysiert worden sind, und sie weisen zudem auch hohe Nickelkonzentrationen auf (200–1700 ppm). In der Stratigraphie treten die Cr-reichen Basalte über dem Komatiit und den komatiitischen Basalteinheiten auf und bilden die obersten Einheiten der Komatiitsequenz. Extrem reduzierende Bedingungen w?hrend der Magmabildung oder fraktionierte Kristallisation werden als eine Ursache für diese au?ergew?hnlichen Zusammensetzungen vorgeschlagen. Die niedrige Sauerstoff-Fugazit?t hat die Kristallisation des Chromits gehemmt, den Verteilungskoeffizienten Olivin/Schmelze für Nickel bei der Olivinfraktionierung herabgesetzt und dadurch die Anreicherung von Cr und Ni in der Restschmelze verursacht.

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Received November 24, 1997; revised version accepted July 22, 1999