Geochemical variations in lavas from Kahoolawe volcano,Hawaii: evidence for open system evolution of plume-derived magmas

The Kahoolawe shield volcano produced precaldera and caldera-filling tholeiites and mildly alkalic post-caldera lavas that petrographically and compositionally resemble such lavas from other Hawaiian shield volcanoes. However, Kahoolawe tholeiites display wide ranges in incompatible trace element ratios (e.g., Nb/Th=9–24, Th/Ta=0.6–1.3), ⁸⁷Sr/⁸⁶Sr (0.70379–0.70440), ¹⁴³Nd/¹⁴⁴Nd (0.51273–0.51298), and ²⁰⁶Pb/²⁰⁴Pb (17.92–18.37). The isotopic variation exceeds that at any other Hawaiian shield volcano, and spans about half the range for all Hawaiian tholeiites. Quasi-cyclic temporal evolution of Kahoolawe tholeiites is consistent with combined fractional crystallization and periodic recharge by primitive magmas. Ratios of highly incompatible trace elements and Sr, Nd, and Pb isotopic ratios from coherent sub-trends that reflect recurrent interactions between variably evolved magmas and two other mantle components whose compositions are constrained by intersections between these trends. The most MgO-rich Kahoolawe tholeiites are partial melts of a high Nb/Th (23.5) ascending plume, possibly comprising ancient subducted oceanic lithosphere. Slightly evolved tholeiites experienced combined crystal fractionation and assimilation (AFC) of material derived from a distinct reservoir (Nb/Th 9) of asthenospheric derivation. The most evolved tholeiites display compositional shifts toward a third component, having mid ocean ridge basalt-like isotopic ratios but enriched OIB-like trace element ratios, representing part of the lithospheric mantle (or melts thereof). Periodic recurrence of all three magma variants suggests that eruptions may have tapped coeval reservoirs distributed over a large depth range. Kahoolawe provides new evidence concerning the nature of the Hawaiian plume, the distribution of compositional heterogeneities in the suboeanic mantle, and the processes by which Hawaiian tholeiites form and evolve.     

Neodymium isotopic composition of Quaternary island arc lavas from Indonesia

${}^{143}\text{Nd}{}^{144}\text{Nd}$ ratios measured in Quaternary lavas from Java and the Banda arc of Indonesia range from 0.51242 to 0.51280 and exhibit an inverse correlation with ${}^{87}\text{Sr}{}^{86}\text{Sr}$. Isotopically, the Indonesian samples resemble Andean rather than island arc lavas. The samples from Java plot either within, or adjacent to the mantle array, towards higher ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios. Samples from the Banda arc and the anomalous calc-alkaline volcano Papandajan are characterized by relatively low ${}^{143}\text{Nd}{}^{144}\text{Nd}$ and high ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios. These characteristics are consistent with the interpretation that subducted terrigenous material was involved in the genesis of these lavas. Furthermore the Banda arc samples appear to lie on a mixing line between isotopic compositions characteristic of the mantle and upper continental crust. A high-K trachyte from the alkaline volcano Muriah, Java, has isotopic characteristics of the mantle (${}^{143}\text{Nd}{}^{144}\text{Nd}\text{= 0.51270}$, ${}^{87}\text{Sr}{}^{86}\text{Sr}\text{= 0.70424}$), which implies that the extreme enrichment in large-ion-lithophile elements in its source must have occurred only shortly before its formation. The inferred ${}^{143}\text{Nd}{}^{144}\text{Nd}$ ratio of the unmodified mantle beneath Java and the Banda arc is lower than that observed in mid-ocean ridge basalt, which may have important implications for a better understanding of the geochemical structure of the mantle.     

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.     

Rubidium,strontium content and strontium isotopic composition of strongly alkalic basaltic rocks from the Cape Verde islands

The Cape Verde islands are characterized by the presence of very strongly alkalic lavas. Cenozoic volcanics—covering the broadest compositional range present in the archipelago—and ranging from alkali-basalts to phonolites, associated with plutonic essexites and nepheline syenites, were analyzed for Sr isotopic compositions and concentrations in K, Rb and Sr. The close values of the Sr⁸⁷/Sr⁸⁶ ratios (ranging from 0.7029 to 0.7033) indicate a comagmatic origin for the different rock types; no correlation appears between the Sr isotopic composition and the K-content of the lavas, thus indicating that the lavas with high K₂O/K₂O + Na₂O ratio are generated from a primary magma by differentiation at shallow depths. The values of the Sr isotopic composition are distinctly lower than most values obtained for lavas of other oceanic islands. The origin of the magma type is discussed on the basis of these isotopic compositions and the K/Rb and Rb/Sr ratios: it is suggested that the primary magma has a nephelinitic composition and was formed by partial melting of a small fraction of undepleted mantle peridotite, containing phlogopite; the deeper part of the mantle where this nephelinitic magma generates would have a strontium isotopic ratio of about 0.703 and a Rb/Sr ratio lower than that of the upper part.     

Strontium isotopic and selected trace element variations between two Aleutian volcanic centers (Adak and Atka): implications for the development of arc volcanic plumbing systems

Major and trace element concentrations and initial ⁸⁷Sr/⁸⁶Sr ratios of lavas from the Aleutian volcanic centers of Adak and Atka have been used to study the evolution of their respective lithospheric plumbing systems. The centers are within 150 km of one another and show similar overall silica ranges (47–67%), but Adak (40 km³) is smaller than Atka (200 km³). Adak's lavas are chemically and isotopically heterogeneous (⁸⁷Sr/⁸⁶Sr:0.70285–0.70330) and two units contain lithospheric xenoliths. The lavas of the much larger Atka, on the other hand, have much less variability in major and trace elements as well as ⁸⁷Sr/⁸⁶Sr (0.70320–0.70345). We suggest that these characteristics are a measure of the relative maturity and cleanliness of the lithospheric plumbing systems that supply magma to these centers. Because Aleutian volcanic centers often remain fixed for relatively long periods of time (5 m.y.), once established, magmatic passageways are repeatedly used. Young plumbing systems are relatively cool and contain large amounts of wallrock contaminant, and ascending magmas undergo contamination as well as concurrent crystallization and fractionation. With time, however, heat and mass transfer between ascending magmas and wallrock produce thermal and chemical boundary layers that insulate subsequent magmas. In effect, the plumbing system matures. The chemical heterogeneity displayed by young, dirty systems (like Adak) reflects not only the magma source but also the wallrock encountered during ascent and possibly the effects of extensive crystal fractionation. Thus, it is the petrologic data of mature, clean systems, like Atka, that yield the most direct and unambiguous information on the ultimate origin of the lavas and their near surface evolution.     

Crystallization of primitive basaltic magmas at crustal pressures and genesis of the calc-alkaline igneous suite: experimental evidence from St Vincent,Lesser Antilles arc

Near-liquidus crystallization experiments have been carried out on two basalts (12.5 and 7.8 wt% MgO) from Soufriere, St Vincent (Lesser Antilles arc) to document the early stages of differentiation in calc-alkaline magmas. The water-undersaturated experiments were performed mostly at 4 kbar, with 1.6 to 7.7 wt% H₂O in the melt, and under oxidizing conditions (ΔNNO = −0.8 to +2.4). A few 10 kbar experiments were also performed. Early differentiation of primitive, hydrous, high-magnesia basalts (HMB) is controlled by ol + cpx + sp fractionation. Residual melts of typical high-alumina basalt (HAB) composition are obtained after 30–40% crystallization. The role of H₂O in depressing plagioclase crystallization leads to a direct relation between the Al₂O₃ content of the residual melt and its H₂O concentration, calibrated as a geohygrometer. The most primitive phenocryst assemblage in the Soufriere suite (Fo_89.6 olivine, Mg-, Al- and Ti-rich clinopyroxene, Cr–Al spinel) crystallized from near-primary (Mg# = 73.5), hydrous (∼5 wt% H₂O) and very oxidized (ΔNNO = +1.5–2.0) HMB liquids at middle crustal pressures and temperatures from ∼1,160 to ∼1,060°C. Hornblende played no role in the early petrogenetic evolution. Derivative HAB melts may contain up to 7–8 wt% dissolved H₂O. Primitive basaltic liquids at Soufriere, St Vincent, have a wide range of H₂O concentrations (2–5 wt%).     

Polybaric differentiation of alkali basaltic magmas: evidence from green-core clinopyroxenes (Eifel,FRG)

The Quaternary foidites and basanites of the West Eifel (Germany) contain optically and chemically heterogeneous clinopyroxenes, some of which occur as discrete zones within individual crystals: Most clinopyroxene phenocrysts are made up of a core and a normally zoned comagmatic titanaugite mantle. Most cores are greenish pleochroic and moderately resorbed (fassaitic augite). Some are pale green and strongly resorbed (acmitic augite). Cores of Al-augite composition and of Cr-diopside derived from peridotite xenoliths are rare. The fassaitic augites are similar in trace element distribution pattern to the titanaugites, but are more enriched in incompatible elements. The acmitic augites, in contrast, are clearly different in their trace element composition and are enriched in Na, Mn, Fe and depleted in Al, Ti, Sr, Zr. A model for polybaric magma evolution in the West Eifel is proposed: Primitive alkali basaltic magma rises through the upper mantle precipitating Al-augite en route. It stagnates and differentiates near the crust/mantle boundary crystallizing Fe-rich fassaitic augites. The magma differentiated at high pressure is subsequently mixed with new pulses of primitive magma from which the rims of pyroxene are crystallized. Sporadic alkali pyroxenite xenoliths are interpreted to represent cumulates of cognate phases formed within the crust and not metasomatized upper mantle material (Lloyd and Bailey 1975).     

Volatile-induced transport of HFSE, REE, Th and U in arc magmas: evidence from zirconolite-bearing vesicles in potassic lavas of Lewotolo volcano (Indonesia)

Potassium-rich calc-alkaline lavas of Lewotolo volcano, situated in the East Sunda Arc, Indonesia, contain the rare mineral zirconolite (CaZrTi₂O₇). Samples in which tiny grains of this mineral (3–25 μm in size) were found span the entire range of lava compositions (47–62 wt% SiO₂). To the best of our knowledge, this is the first record of primary zirconolite in juvenile arc volcanics. The mineral forms part of a vesicle-filling assemblage consisting of a network of quenched feldspar crystals and an SiO₂ phase, probably cristobalite. High contents of Th, U and REE (up to 9.3, 4.3 and 15.6 wt% oxide respectively) and very high Fe contents (up to 13.5 wt% Fe₂O₃) distinguish these zirconolites from those of other rock types. The extraction of volatile-rich phases with changing compositions in successive stages is considered to be responsible for the zirconolite formation. We hypothesise that a fluid capable of transporting HFSE, REE, Th and U was extracted from the magma and (partly) crystallised within voids which had formed earlier upon saturation of an aqueous fluid. Assuming that zirconolite compositions largely reflect trace metal contents of the coexisting fluid phase, significant amounts of `immobile' elements must have been transported on a macroscopic scale. Our findings thus point to a late-stage transfer of HFSE, REE, Th and U between different domains in a cooling magma body. Such a volatile-induced redistribution of trace elements at shallow levels of high-K volcanic systems may be significant for conventional geochemical modelling of magma evolution and for Th–U disequilibrium studies. Received: 3 November 1999 / Accepted: 29 February 2000     

Origin of late-cenozoic lavas from the Banda arc,Indonesia: Trace element and Sr isotope evidence

The Banda arc of eastern Indonesia manifests the collision of a continent and an intra-oceanic island arc. The presently active arc is located on what appears to be oceanic crust whereas the associated subduction trench is underlain by continental crust.Recent lavas from the Banda arc are predominantly andesitic and range from tholeiitic in the north through calc-alkaline to high-K calc-alkaline varieties in the southern islands. Defining this regular geochemical variation are significant increases in the abundances of K (2,600–21,000 ppm), Rb (10–90 ppm), Cs (0.5–7.0 ppm), and Ba (100–1,000 ppm) from tholeiitic to high-K calc-alkaline lavas. ⁸⁷Sr/⁸⁶Sr ratios in the tholeiites are relatively low, from 0.7045 to 0.7047. In the calc-alkaline lavas, ⁸⁷Sr/⁸⁶Sr ratios range from 0.7052 to 0.7095, and in the high-K calc-alkaline lavas from 0.7065 to 0.7080. There is no correlation between ⁸⁷Sr/⁸⁶Sr and major and trace element abundances, even among lavas from the same volcano. Late Cenozoic cordierite — bearing lavas from Ambon, north of the presently active arc, are highly enriched in K, Rb and Cs, which together with ⁸⁷Sr/⁸⁶Sr ratios of approximately 0.715 is consistent with their derivation from partial melting of pelitic material in the locally — thick crust.The high ⁸⁷Sr/⁸⁶Sr ratios in the Recent calc-alkaline lavas are interpreted to result from mixing of a sialic component with a mantle derived component. The most likely cause is subduction and subsequent melting of either sea-floor sediments or continental crust. However, it is probably unrealistic to model this type of deep contamination by simple two-component mixing. Such contamination implies that the volcanic rocks from the Banda arc are at least partly a manifestation of melting at or near the Benioff seismic zone. Temperatures of at least 750–800 ° C at the top of the subducted lithospheric slab at depths of approximately 150 km are also implied; temperatures very close to the solidus of hydrous basalt (eclogite) at such pressure. It is concluded that partial melting of the crustal component of the subducted lithospheric slab may play a significant role in island arc petrogenesis.This paper is the result of a cooperative project with the Geological Survey of Indonesia, Ministry of Mines and Energy     

Phase relations governing the derivation of alkaline basaltic magmas from primary magmas at high pressures

A comparison between the variation trend of alkaline basaltic magmas within the CaO-MgO-Al₂O₃-SiO₂ system and experimentally estimated phase relations for this system at high pressures, suggests an olivine reaction relationship, which may explain the transition from primary magmas in equilibrium with olivine to alkaline basaltic magmas in which olivine does not form at high pressures. This reaction relationship is considered to be due to a transition from positive to negative crystallization with respect to olivine along the four phase curve where olivine, diopside, pyrope garnet and liquid are initially in equilibrium. The bimineralic, eclogitic character of alkaline basaltic compositions at high pressures is interpreted as being due to the presence of a thermal minimum on the three phase surface, where dioside and pyrope garnet are in equilibrium with liquid.     

The rheology of crystal-bearing basaltic magmas from Stromboli and Etna

Our ability to forecast volcanic hazards at active volcanoes stems from our knowledge of parameters affecting eruption dynamics. Persistent activity displayed by basaltic volcanic systems, such as Etna and Stromboli, is governed mainly by the textural evolution and rheological properties of eruptive products. Here, we investigate the high temperature (1131 °C < T < 1187 °C) rheological behavior and textural evolution of remelted natural basaltic magmas from Stromboli and Etna volcanic systems upon cooling and crystallization at atmospheric conditions. The pure liquid and subliquidus isothermal viscosities are investigated using a concentric cylinder apparatus by varying strain rate applied to the investigated materials. Detailed textural analysis has been performed in order to evaluate the effect of crystal distribution on the rheological evolution of magmas. At subliquidus conditions, the mineralogical assemblage is dominated by the presence of spinel and plagioclase with the occurrence of stable clinopyroxene only at the lowest temperatures (1157 and 1131 °C for the Stromboli and the Etna samples, respectively). The overall crystal fraction (?) varies between 0.06 and 0.27. In the high T regime the viscous response to applied stress and strain rate is strongly affected by the presence of even small amounts of crystals. Large discrepancies between measured and predicted viscosities obtained using the Einstein-Roscoe (ER) equation are also found at low crystal fractions. We find here that, at the investigated conditions, the physical effect caused by the presence of elongated crystals is orders of magnitude higher than that predicted by existing models which only account for spherical particles. It also appears that a weak shear thinning behavior occurs at the lowest temperatures investigated. Crystal shape and, with it, the strain-rate dependence of the rheological properties appear to play primary roles in influencing the transport properties of these basaltic magmas.     

Mid-Pleistocene lavas from the Seguam volcanic center,central Aleutian arc: closed-system fractional crystallization of a basalt to rhyodacite eruptive suite

In contrast to adjacent volcanic centers of the modern central Aleutian arc, Seguam Island developed on strongly extended arc crust. K-Ar dates indicate that mid-Pleistocene, late-Pleistocene, and Holocene eruptive phases constitute Seguam. This study focuses on the petrology of the mid-Pleistocene, 1.07–07 Ma, Turf Point Formation (TPF) which is dominated by an unusual suite of porphyritic basalt and basaltic andesite lavas with subordinate phenocryst-poor andesite to rhyodacite lavas. Increasing whole-rock FeO^*/MgO from basalt to dacite, the anhydrous Plag+Ol+Cpx±Opx±Mt phenocryst assemblage, groundmass pigeonite, and the reaction Ol+Liq=Opx preserved in the mafic lavas indicate a tholeiitic affinity. Thermometry and comparison to published phase equilibria suggests that most TPF basalts crystallized Plag+Ol+Cpx±Mt at 1160°C between about 3–5 kb (±1–2% H₂O), andesites crystallized Plag+Cpx+Opx±Mt at 1000°C between 3–4 kb with 3–5% H₂O, and dacites crystallized Plag +Cpx±Opx±Mt at 1000°C between 1–2 kb with 2–3% H₂O. All lavas crystallized at f _{o 2} close to the NNO buffer. Mineral compositions and textures indicate equilibrium crystallization of the evolved lavas; petrographic evidence of open-system mixing or assimilation is rare. MgO, CaO, Al₂O₃, Cr, Ni, and Sr abundances decrease and K₂O, Na₂O, Rb, Ba, Zr, and Pb increase with increasing SiO₂ (50–71%). LREE enrichment [(Ce/Yb)_n=1.7±0.2] characterizes most TPF lavas; total REE contents increase and Eu anomalies become more negative with increasing SiO₂. Relative to other Aleutian volcanic centers, TPF basalts and basaltic andesites have lower K₂O, Na₂O, TiO₂, Rb, Ba, Sr, Zr, Y, and LREE abundances. ⁸⁷Sr/⁸⁶Sr ratios (0.70361–0.70375) and ratios of ²⁰⁶Pb/²⁰⁴Pb (18.88–18.97), ²⁰⁷Pb/²⁰⁴Pb (15.58–15.62), ²⁰⁸Pb/²⁰⁴Pb (38.46–38.55) are the highest measured for any suite of lavas in the oceanic portion of the Aleutian arc. Conversely, Nd values (+5.8 to+6.7) are among the lowest from the Aleutians. Sr, Nd, and Pb ratios are virtually constant from basalt through rhyodacite, whereas detectable isotopic heterogenity is observed at most other Aleutian volcanic centers. Major and trace element, REE, and Sr, Nd, and Pb isotopic compositions are consistent with the basaltic andesitic, andesitic, dacitic, and rhyodacitic liquids evolving from TPF basaltic magma via closed-system fractional crystallization alone. Fractionation models suggest that removal of 80 wt% cumulate (61% Plag, 17% Cpx, 12% Opx, 7% Ol, and 3% Mt) can produce 20 wt% rhyodacitic residual liquid per unit mass of parental basaltic liquid. Petrologic and physical constraints favor segregation of small batches of basalt from a larger mid-crustal reservoir trapped below a low-density upper crustal lid. In these small magma batches, the degree of cooling, crystallization, and fractionation are functions of the initial mass of basaltic magma segregated, the thermal state of the upper crust, and the magnitude of extension. Tholeiitic magmas erupted at Seguam evolved by substantially different mechanisms than did calc-alkaline lavas erupted at the adjacent volcanic centers of Kanaga and Adak on unextended arc crust. These variable differentiation mechanisms and liquid lines of descent reflect contrasting thermal and mechanical conditions imposed by the different tectonic environments in which these centers grew. At Seguam, intra-arc extension promoted eruption of voluminous basalt and its differentiates, unmodified by interaction with lower crustal or upper mantle wallrocks.     

Origin and differentiation of recent basaltic magmas from Mount Etna

Summary One hundred and fifty samples of recent Na-alkalic lavas from the south-eastern flank of Mt. Etna, dating from about 5,000 years B.P. to 1886 were analyzed. They grade in time from more acid to more basic lavas, and show an overall range of variation much larger toward the more felsic end than previously known. Chondrite-normalized REE patterns of the least differentiated samples show LREE enrichment and HREE depletion; trace element compositions suggest that Etnean products are similar to WPB, with a weak CAB signature. Sr-isotope ratios ranging from 0.70332 to 0.70355, vary even within samples from the same eruption, and generally tend to increase with time in historic lavas.Our data suggest that processes other than simple crystal fractionation are, in part, responsible for the variation of the analyzed sequence. In fact, RTF processes with successive influxes of mafic melts, each having distinct, slightly different geochemical and isotopic features, into reservoirs of variously differentiated magmas, may explain the overall observed data.The source region for Recent Mongibello lavas is located in the mantle, isotopically zoned, and Rb-depleted with respect to the Bulk Earth composition. Model and experimental data conform well with a low degree (< 5%) modal melting of a garnet Iherzolite source, depleted by an earlier melting event with respect to primitive mantle composition.

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Herkunft und Differentiation von rezenten basaltischen Magmen des Berges Ätna

Zusammenfassung Es wurden 150 Proben von rezenten, Na-alkalischen Laven von der Südflanke des Ätna, die mit 5000 Jahren vor Christus bis 1886 datieren, analysiert. Die Laven zeigen mit der Zeit einen graduellen Übergang von sauer zu zunehmend basisch und weisen generell eine größere Variationsbreite in Richtung sauer auf als bisher angenommen. Chondrit-normalisierte REE Verteilungskurven der am geringsten differentierten Proben zeigen LREE Anreicherung und eine Verarmung der HREE. Die Spurenelement-Zusammensetzungen deuten an, daß die Ätna-Produkte Ähnlichkeit mit WPB mit einer schwachen CAB-Signatur aufweisen. Die Sr-Isotopenverhältnisse reichen von 0.70332 bis 0.70355, variieren sogar innerhalb Proben aus ein und derselben Eruption und tendieren generell zu ansteigenden Werten mit der Zeit.Unsere Daten weisen darauf hin, daß andere Prozesse als einfache Kristallfraktionierung, zumindest teilweise, für die Variation der analysierten Sequenz verantwortlich sind. In der Tat können RTF Prozesse mit sukzessiver Zufuhr von mafischen Schmelzen, jede mit leicht unterschiedlicher Geochemie und definierten Isotopenverhältnissen, in Reservoirs von unterschiedlich differentiierten Magmen, die vorliegenden Daten erklären.Die Herkunftsregion der rezenten Mongibello Laven ist im Mantel angesiedelt, der bezüglich der Isotopenzusammensetzung zoniert und, verglichen mit der Erdzusammensetzung, an Rb verarmt ist. Die Modell- und experimentellen Daten stehen in guter Übereinstimmung mit einem niedrigen Grad ( < 5%) der Aufschmelzung eines Granat-Lherzolites als Ausgangsmaterial, das, im Vergleich zum primitiven Mantel, durch einen früheren Aufschmelzungsvorgang verarmt ist.

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With 9 Figures     

The origin of medium-K ankaramitic arc magmas from Lombok (Sunda arc, Indonesia): Mineral and melt inclusion evidence

High-calcium, nepheline-normative ankaramitic basalts (MgO > 10 wt.%, CaO/Al₂O₃ > 1) from Rinjani volcano, Lombok (Sunda arc, Indonesia) contain phenocrysts of clinopyroxene and olivine (Fo_85–92) with inclusions of spinel (Cr# 58–77) and crystallised melt. Olivine crystals have variable but on average low NiO (0.10–0.23 wt.%) and high CaO (0.22–0.35 wt.%) contents for their forsterite number. The CaO content of Fo_89–91 olivine is negatively correlated with the Al₂O₃ content of enclosed spinel (9–15 wt.%) and positively correlated with the CaO/Al₂O₃ ratios of melt inclusions (0.9–1.5). Major and trace element patterns of melt inclusions are similar to that of the host rock, indicating that the magma could have formed by accumulation of small batches of melt, with compositions similar to the melt inclusions. The liquidus temperature of the magma was  1275 °C, and its oxygen fugacity ≤ FMQ + 2.5. Correlations between K₂O, Zr, Th and LREE in the melt inclusions are interpreted to reflect variable degrees of melting of the source; correlations between Al₂O₃, Na₂O, Y and HREE are influenced by variations in the mineralogy of the source. The melts probably formed from a water-poor, clinopyroxene-rich mantle source.     

Evolution of basaltic and differentiated lavas from Anjouan,Comores Archipelago

Anjouan is one of four volcanic islands comprising the Comores Archipelago. Three (arbitrarily defined) categories of basic magma are recognised on Anjouan: ‘hypersthenenormative’, ‘alkalic’ and ‘basanitic’, which appear in that order with an eruptive sequence involving 1) shield construction, 2) peripheral fissure-controlled activity, and 3) rejuvenescent (posterosional) eruptions. Differentiated magmas have evolved within the three chemical groupings, and trend mainly towards undersaturated trachyte and phonolite. These trends are considered to have developed by initial removal of olivine and clinopyroxene, followed by Fe-Ti oxides, apatite and amphibole from arrested liquid pools within and beneath the volcano. The appearance of feldspar on the liquidus was clearly inhibited by the high contents of normative diopside in most Anjouan magmas, although late stage plagioclase fractionation is probably responsible for development of peralkaline phonolites at shallow depths, assisted eventually by alkali feldspar. Lherzolite-xenolith-bearing lavas are likely to be directly mantle-derived liquids. Three analysed representatives with 100 · Mg/Mg + Fe²⁺ (atomic) ratios approaching 70 are characteristically rich in normative diopside and may confirm the suggestion of primitive ankaramitic melts in mantle regions. High pressure fractional crystallisation may involve fractionation of ‘eclogite’, orthopyroxene or clinopyroxene, with or without olivine. It is believed however that such processes do not adequately explain the compositional change from hypersthene-normative basalt towards basanite, as they imply unacceptable degrees of Fe-enrichment. Problems of large ion element enrichment and fractionation would also remain, while the high contents of Cr and Ni place limits on the extent of crystal fractionation. A partial melting model of magma genesis is able to explain the main features of basalt geochemistry, especially if the upper mantle low velocity zone is regarded as having been severely fractionated due to upward migration of large ion elements. An ‘open’ system of magma production in the context of regional plate movement, and the implied decoupling between lithosphere and asthenosphere, accomodates realistic degrees of partial melting and allows a greater potential volume of mantle available for melting than possible ‘closed’ systems. The model also accounts for the migratory pattern of Comores volcanism.     

Tachylyte in Cenozoic basaltic lavas from the Czech Republic and Iceland: contrasting compositional trends

Mineralogy and Petrology - Tachylytes from rift-related volcanic rocks were recognized as: (i) irregular veinlets in host alkaline lava flows of the Kozákov volcano, Czech Republic, (ii)...     

Temporal evolution of the kerguelen plume: Geochemical evidence from 38 to 82 ma lavas forming the Ninetyeast ridge

Abstract Basaltic basement has been recovered by deep-sea drilling at seven sites on the linear Ninetyeast Ridge in the eastern Indian Ocean. Studies of the recovered lavas show that this ridge formed from ~ 82 to 38 Ma as a series of subaerial volcanoes that were created by the northward migration of the Indian Plate over a fixed magma source in the mantle. The Sr, Nd and Pb isotopic ratios of lavas from the Ninetyeast Ridge range widely, but they largely overlap with those of lavas from the Kerguelen Archipelago, thereby confirming previous inferences that the Kerguelen plume was an important magma source for the Ninetyeast Ridge. Particularly important are the ~ 81 Ma Ninetyeast Ridge lavas from DSDP Site 216 which has an anomalous subsidence history (Coffin 1992). These lavas are FeTi-rich tholeiitic basalts with isotopic ratios that overlap with those of highly alkalic, Upper Miocene lavas in the Kerguelen Archipelago. The isotopic characteristics of the latter which erupted in an intraplate setting have been proposed to be the purest expression of the Kerguelen plume (Weis et al. 1993a,b). Despite the overlap in isotopic ratios, there are important compositional differences between lavas erupted on the Ninetyeast Ridge and in the Kerguelen Archipelago. The Ninetyeast Ridge lavas are dominantly tholeiitic basalts with incompatible element abundance ratios, such as La/Yb and Zr/Nb, which are intermediate between those of Indian Ocean MORB (mid-ocean ridge basalt) and the transitional to alkalic basalts erupted in the Kerguelen Archipelago. These compositional differences reflect a much larger extent of melting for the Ninetyeast Ridge lavas, and the proximity of the plume to a spreading ridge axis. This tectonic setting contrasts with that of the recent alkalic lavas in the Kerguelen Archipelago which formed beneath the thick lithosphere of the Kerguelen Plateau. From ~ 82 to 38 Ma there was no simple, systematic temporal variation of Sr, Nd and Pb isotopic ratios in Ninetyeast Ridge lavas. Therefore all of the isotopic variability cannot be explained by aging of a compositionally uniform plume. Although Class et al. (1993) propose that some of the isotopic variations reflect such aging, we infer that most of the isotopic heterogeneity in lavas from the Ninetyeast Ridge and Kerguelen Archipelago can be explained by mixing of the Kerguelen plume with a depleted MORB-like mantle component. However, with this interpretation some of the youngest, 42–44 Ma, lavas from the southern Ninetyeast Ridge which have²⁰⁶pb/²⁰⁴Pb ratios exceeding those in Indian Ocean MORB and Kerguelen Archipelago lavas require a component with higher²⁰⁶Pb/²⁰⁴Pb, such as that expressed in lavas from St. Paul Island.