Upper mantle source for some hawaiites,mugearites and benmoreites

Chemical analyses of over seventy lavas or dykes containing spinel lherzolite inclusions of high pressure mineralogy, show that most host magmas are of alkali olivine basalt or basanite composition with relatively rare olivine nephelinites, and olivine melilitites. The 100 Mg/Mg+Fe⁺⁺ ratios of host magmas display a strong maximum at about Mg₇₀ consistent with partial melting of source peridotite with olivine of Fo_88–90. In contrast to these primary magmas, there occur some host magmas with 100 Mg/Mg+Fe⁺⁺<60 and with chemical compositions resembling those of classical hawaiite, mugearite, and nepheline benmoreite magmas. It is inferred that these magmas have been produced by crystal fractionation, within the upper mantle, of parental basanites or alkali olivine basalts. The presence of kaersutitic hornblende xenocrysts accompanying the lherzolite inclusions, and the nature of the chemical variation between associated basanites and nepheline benmoreites suggests that crystal fractionation has been dominated by kaersutitic hornblende, together with olivine and, in some cases, probably clinopyroxene. The mantle-derived nepheline benmoreite magmas also show similarities to some plutonic nepheline syenites.     

Petrologic Evolution of Anorthoclase Phonolite Lavas at Mount Erebus, Ross Island, Antarctica

Mount Erebus, Ross Island, Antarctica, is an active, intraplate,alkaline volcano. The strongly undersaturated sodic lavas rangefrom basanite to anorthoclase phonolite, and are termed theErebus lineage (EL). The lavas are porphyritic with olivine(Fo₈₈–51), clinopyroxene (Wo₄₅–53En₃₆–41Fs₈–30),opaque oxides (Usp₃₁–76), feldspar (An₇₂–11), andapatite. Rare earth element (REE) contents increase only slightlywith increasing differentiation compared with other incompatibleelements. The light REE are enriched (La_N/Yb_N= 14–20)and there are no significant Eu anomalies. ⁸⁷Sr/⁸⁶Sr is uniformand low ({small tilde} 0.7030) throughout the EL, suggestingderivation of the basanites from a depleted asthenospheric mantlesource, and lack of significant crustal contamination duringfractionation of the basanite. Regular geochemical trends indicatethat the EL evolved from the basanites by fractional crystallization.Major element mass balance calculations and trace element modelsshow that fractionation of 16% olivine, 52% clinopyroxene, 14%Fe-Ti oxides, 11% feldspar, 3% nepheline, and 3% apatite froma basanite parent leaves 23.5% anorthoclase phonolite. Minor volumes of less undersaturated, more iron-rich benmoreite,phonolite, and trachyte are termed the enriched iron series(EFS). The trachytes have ⁸⁷Sr/⁸⁶Sr of 0.704, higher than otherEFS and EL rocks, and they probably evolved by a combined assimilation-fractionalcrystallization process. The large volume of phonolite at Mt. Erebus requires significantbasanite production. This occurs by low degrees of partial meltingin a mantle plume (here termed the Erebus plume) rising at arate of about 6 cm/yr.     

Magma storage and ascent during the 1995 eruption of Fogo,Cape Verde Archipelago

The 1995 eruption of Fogo (Cape Verde Islands) differed from previous eruptions by the occurrence of evolved lavas, the SW-orientation of vents, and pre-eruptive seismicity between Fogo and the adjacent (~20 km) island of Brava. We have conducted a thermobarometric and chemical study of this eruption in order to reconstruct its magma plumbing system and to test for possible connections to Brava. The bimodal eruption produced basanites (5.2–6.7 wt% MgO) and phonotephrites (2.4–2.8 wt% MgO) that are related by fractional crystallization. Clinopyroxene-melt-barometry of phenocrysts yields pressure ranges of 460–680 MPa for the basanites and 460–520 MPa for the phonotephrites. Microthermometry of CO₂-dominated fluid inclusions in olivine and clinopyroxene phenocrysts yields systematically lower pressure ranges of 200–310 MPa for basanites and 270–470 MPa for phonotephrites. The combined data indicate pre-eruptive storage of the 1995 magmas within the lithospheric mantle between 16 and 24 km depth. During eruption, the ascending magmas stalled temporarily at 8–11 km depth, within the lower crust, before they ascended to the surface in a few hours as indicated by zonations of olivine phenocrysts. Our data provide no evidence for magma storage at shallow levels (<200 MPa) or lateral magma movements beneath the Fogo-Brava platform. Sr–Nd–Pb isotope ratios of samples from Brava differ significantly from those of the 1995 and older Fogo lavas, which rules out contamination of the 1995 magmas by Brava material and indicates different mantle sources and magma plumbing systems for both islands.     

Melt evolution during the crystallization of basanites of the Tergesh pipe,northern Minusinsk Depression

In this paper we describe the mineralogy and geochemistry of basanites and melt inclusions in minerals from the Tergesh pipe, northern Minusinsk Depression. The rocks are composed of olivine and clinopyroxene phenocrysts and a groundmass of olivine, clinopyroxene, titanomagnetite, plagioclase, apatite, ilmenite, and glass. Melt inclusions were found only in the olivine and clinopyroxene phenocrysts. Primary melt inclusions in olivine contain glass, rh?nite, clinopyroxene, a sulfide globule, and low-density fluid. The phase composition of melt inclusions in clinopyroxene is glass + low-density fluid ± xenogenous magnetite. According to thermometric investigations, the olivine phenocrysts began crystallizing at T = 1280–1320°C and P > 3.5 kbar, whereas groundmass minerals were formed under near-surface conditions at T ≤ 1200°C. The oxygen fugacity gradually changed during basanite crystallization from oxidizing (NNO) to more reducing conditions (QFM). The investigation of glass compositions (heated and unheated inclusions in phenocrysts and groundmass) showed that the evolution of a basanite melt during its crystallization included mainly an increase in SiO₂, Al₂O₃, and alkalis, while a decrease in femic components, and the melt composition moved gradually toward tephriphonolite and trachyandesite. Geochemical evidence suggests that the primary basanite melt was derived from a mantle source affected by differentiation. Original Russian Text ? T.Yu. Timina, V.V. Sharygin, A.V. Golovin, 2006, published in Geokhimiya, 2006, No. 8, pp. 814–833.     

Cognate clinopyroxene from Paleogene mantle xenolith-bearing basanite lavas (East Serbia, SE Europe): the role of dissolution of mantle orthopyroxene

The study focuses on clinopyroxene from mantle xenolith-bearing East Serbian basanites and suggests that dissolution of mantle orthopyroxene played an important role in at least some stages of the crystallization of these alkaline magmas. Five compositional types of clinopyroxene are distinguished, some of them having different textural forms: megacrysts (Type-A), green/colourless-cored phenocrysts (Type-B), overgrowths and sieve-textured cores (Type-C), rims and matrix clinopyroxene (Type-D), and clinopyroxene from the reaction rims around orthopyroxene xenocrysts (Type-E). Type-A is high-Al diopside that probably crystallized at near-liquidus conditions either directly from the host basanite or from compositionally similar magmas in previous magmatic episodes. Type-B cores show high ^VIAl/^IVAl≥1 and low Mg# of mostly <75 and are interpreted as typical xenocrysts. Type-C, D and E are interpreted as typical cognate clinopyroxene. Type-D has Mg#<78, Al₂O₃?=?6–13?wt.%, TiO₂?=?1.5–4.5?wt.%, and Na₂O?=?0.4–0.8?wt.% and compositionally similar clinopyroxene is calculated by MELTS as a phase in equilibrium with the last 30?% of melt starting from the average host lava composition. Type-C has Mg#?=?72–89, Al₂O₃?=?4.5–9.5?wt.%, TiO₂?=?1–2.5?wt.%, Na₂O?=?0.35–1?wt.% and Cr₂O₃?=?0.1–1.5?wt.%. This clinopyroxene has some compositional similarities to Type-E occurring exclusively around mantle orthopyroxene. Cr/Al vs Al/Ti and Cr/Al vs Na/Ti plots revealed that Type-C clinopyroxene can crystallize from a mixture of the host basanite magma and 2–20?wt.% mantle orthopyroxene. Sieve-textured Type-C crystals show characteristics of experimentally produced skeletal clinopyroxene formed by orthopyroxene dissolution suggesting that crystallization of Type-C was both texturally and compositionally controlled by orthopyroxene breakdown. According to FeO/MgO^cpx/melt modelling the first clinopyroxene precipitating from the host basanite was Type-A (T?~?1250?°C, p?~?1.5?GPa). Dissolution of orthopyroxene produced decreasing FeO/MgO^melt and crystallization of Type-E and sieve-textured Type-C clinopyroxene (0.3–0.8?GPa and 1200–1050?°C). The melt composition gradually shifted towards higher FeO/MgO^melt ratios precipitating more evolved Type-C and Type-D approaching near-solidus conditions (<0.3?GPa; ~950?°C).     

Petrogenesis and evolution of Mt. Vulture alkaline volcanism (Southern Italy)

Summary The Late Pleistocene Mt. Vulture strato-volcano developed at the intersection of NE-SW and NW-SE lithospheric fault systems, on the easternmost border of the Apennine compressional front overthrust onto the Apulian foreland. The initial phase of the volcanic activity is represented by pyroclastic deposits, including lava blocks, and subordinate eccentric domes, mostly phonolitic in composition. The later stages of activity formed the bulk of the strato-volcano (pyroclastic products and subordinate lavas), mostly tephritic in composition, with minor intercalations of basanite, mela-foidite and melilitite lavas and dikes. Variations in rock and mineral composition suggest that the volumetrically predominant basanite-tephrite (foidite)-phonotephrite-phonolite series can be accounted for by fractional crystallization processes starting from basanitic parental magmas, in agreement with the remarkably constant ⁸⁷Sr/⁸⁶Sr isotopes (0.70586–0.70581). Mass-balance calculations indicate that the variably differentiated magmas may have been produced by removal of wehrlite, clinopyroxenite and syenite cumulates, some of which are occasionally found as cognate xenoliths in the volcanics. Fractionation processes probably developed in multiple-zoned magma chambers, at depths of 3–5 km, corresponding to the tectonic discontinuity between the allochthonous Apennine formations and the underlying Apulian platform. Highly differentiated phonolitic magmas capping the magma chambers and their conduits thus appear to have fed the initial volcanic activity, whereas dominantly tephritic products were erupted in later stages. The least evolved mafic magmas, namely basanites, mela-foidites and melilitites, are characterized by diverse Na/K ratios and critical SiO₂-undersaturation, which indicate their derivation as independent melts generated from distinct, heterogeneously enriched mantle sources and by variable partial melting degrees. Primitive mantle-normalized incompatible element patterns of Vulture mafic lavas invariably share analogies with both orogenic subduction-related magmas (high Low Field Strength Elements/High Field Strength Elements ratios, K, Rb and Th contents and marked Ti and Nb negative anomalies) and alkaline lavas from within-plate and rift settings (high Light Rare Earth Elements, P, Zr, Nb and Na). These geochemical features may be accounted for by magma generation from deep lithospheric mantle sources, enriched in Na-alkali silicate/carbonatite anorogenic components, subsequently affected by orogenic subduction-related K-metasomatism, analogous to that which modified magma sources of the Roman Magmatic Province along the internal Apennine Chain. Received April 12, 2000; revised version accepted June 7, 2001     

Western Kamchatka-Koryak continental-margin volcanogenic belt: Age,composition, and sources

The isotope-geochemical study of the Eocene-Oligocene magmatic rocks from the Western Kamchatka-Koryak volcanogenic belt revealed a lateral heterogeneity of mantle magma sources in its segments: Western Kamchatka, Central Koryak, and Northern Koryak ones. In the Western Kamchatka segment, magmatic melts were generated from isotopically heterogeneous (depleted and/or insignificantly enriched) mantle sources significantly contaminated by quartz-feldspathic sialic sediments; higher ⁸⁷Sr/⁸⁶Sr (0.70429–0.70564) and lower ¹⁴³Nd/¹⁴⁴Nd(ɛ_Nd(T) = 0.06–2.9) ratios in the volcanic rocks from the Central Koryak segment presumably reflect the contribution of enriched mantle source; the high positive ɛ_Nd(T) and low ⁸⁷Sr/⁸⁶Sr ratios in the magmatic rocks from the Northern Koryak segment area indicate their derivation from isotopically depleted mantle source without significant contamination by sialic or mantle material enriched in radiogenic Sr and Nd. Significantly different contamination histories of the Eocene-Oligocene mantle magmas in Kamchatka and Koryakia are related to their different thermal regimes: the higher heat flow beneath Kamchatka led to the crustal melting and contamination of mantle suprasubduction magmas by crustal melts. The cessation of suprasubduction volcanism in the Western Kamchatka segment of the continentalmargin belt was possibly related to the accretion of the Achaivayam-Valagin terrane 40 Ma ago, whereas suprasubduction activity in the Koryak segment stopped due to the closure of the Ukelayat basin in the Oligocene time.     

Geochemistry of Pliocene/Pleistocene basalts along the Central Anatolian Fault Zone (CAFZ), Turkey

Abstract

Pliocene-Pleistocene volcanism accompanied strike-slip-related transtensional deformation along the K?z?l?rmak fault segment of the Central Anatolian fault zone (CAFZ) in the west of ?ark??la (Sivas-central Turkey). These volcanic rocks are represented by alkali olivine basalts. They can be divided into four different sub-groups on the basis of their Zr, Nb, TiO₂ contents. A primitive mantle-normalized incompatible trace element diagram for four subgroups shows close similarity to typical OIB pattern. Some of the incompatible trace element ratios (Ce/Y, Zr/Nb, La/Ba, La/Nb) are also akin to OIB values. Highly fractionated REE patterns (La/Yb_N=24.7–9.2) with no Eu anomaly are the main features of the alkali basalts and are comparable to alkaline volcanism in continental rift zones. On the basis of Al₂O₃/TiO₂, Nb/Y, Zr/Y Zr/Nb ratios, the geochemical differences among four sub-groups can be explained by variable degrees of partial melting of compositionally similar mantle source. Th/Nb, Th/Y, Nb/Y ratios and the primitive mantle-normalized trace element diagram suggests significant amount of crustal involvement for most of the alkali olivine basalts erupted along the CAFZ. Rupture of the continental lithosphere by strike-slip-related transtensional deformation might have caused decompressional partial melting of the asthenospheric mantle and generating alkali olivine basalts in this region. © 2001 Éditions scientifiques et médicales Elsevier SAS.     

The Geochemistry and Experimental Petrology of Sodic Alkaline Basalts from Oatlands, Tasmania

Sodic basalts of Oligocene-Early Micene age occur within anEarly Tertiary graben in the Oatlands district of Tasmania.They include olivine tholeiites, alkali olivine basalts, basanites,transitional nephelinites, nepheline hawaiites, and nephelinemugearites. They have compositional characteristics in commonwith sodic alkaline basalt suites from other parts of the world.With decreasing SiO₂, concentrations of CaO, alkalis, P₂O₅,and incompatible trace elements increase. Compositional and experimental data for the basalts are consistentwith their derivation by polybaric partial melting of a garnetlherzolite source enriched in P₂O₅, light rare earths, Nb, andother incompatible trace elements. Experimental data for a primitivenepheline basanite from the Oatlands district indicate thatconcentrations of H₂O+CO₂ need not have been more than 6?5 wt.%for the original basanite magma to have derived from an amphibole-bearinggarnet lherzolite source. In the case of more SiO₂-undersaturatedolivine melilitites from the neighbouring Central Plateau, theexperimental evidence is consistent with either higher concentrationsof H₂O+CO₂ (approaching 14 wt.%), or higher pressures of origin(>35 kb). Petrographic and geochemical evidence suggeststhat the latter is the more probable of the alternatives.     

Geochemical characteristics of the high- and low-Ti basaltic rocks from the uplifted shoulder of the Ohře (Eger) Rift,Western Bohemia

High-Ti melanephelinite (3.8–5.9 wt% TiO₂), medium-Ti (phono)tephrite (2.7–3.1 wt% TiO₂), and low-Ti olivine melanephelinite/basanite (1.9–2.3 wt.% TiO₂) are subordinate rock types in the central European Cenozoic Volcanic Province. A contrasting melanephelinite to (phono)tephrite series occurs in the Lou?ná–Oberwiesenthal Volcanic Centre (37–28 Ma) and also as satellite volcanic bodies (26–12 Ma) together with olivine melanephelinite/basanite (17–20 Ma) on the southwestern periphery of the Kru?né hory mountains (Erzgebirge). The volcanic rocks intrude the Variscan basement of the uplifted shoulder of the Oh?e/Eger Rift in the Kru?né hory mountains of the Bohemian Massif. Low Mg# (44–59) and Cr, Ni contents and enrichment of LILE, Zr, Hf, Nb, Ta, U, Th and LREE in the high-Ti melanephelinites contrast with the composition of primitive low-Ti olivine melanephelinites/basanites displaying high Mg# (63–74) and high contents of compatible elements. The high-Ti melanephelinites reveal a wide range in initial ⁸⁷Sr/⁸⁶Sr of ca. 0.7034–0.7038 and ε_Nd of 2.4–4.9. The low-Ti melanephelinites show an overlapping range of initial ⁸⁷Sr/⁸⁶Sr of ca. 0.7035–0.7036 and ε_Nd of 4.3–5.5. The large variation in initial ⁸⁷Sr/⁸⁶Sr ratios at similar ε_Nd values in those rock types is interpreted as evidence for melting of metasomatized lithospheric mantle sources comprising K-bearing phases with radiogenic Sr. Modification of the olivine-free alkali basaltic magmas by differentiation or crustal contamination could give rise to the medium-Ti (phono) tephrites. The initial isotope ratios of all samples are consistent with HIMU-mantle sources and contributions from lithospheric mantle. The olivine-free melanephelinitic rocks often contain alkali pyroxenite–ijolite xenoliths with initial ⁸⁷Sr/⁸⁶Sr ratios of ca. 0.7036 and ε_Nd of 3.0. We interpret these xenoliths as samples of an intra-crustal alkali complex derived from similar mantle sources as those for the basaltic volcanic rocks.     

Average composition of basic magmas and mantle sources of island arcs and active continental margins estimated from the data on melt inclusions and quenched glasses of rocks

Based on the generalization of data on melt inclusions and quenched glasses, the average compositions of subduction (island arc and active continental margin settings) basic magmas were estimated. The main geochemical features of the average composition of these magmas are significant depletion in Nb and Ta, less significant depletion in Ti, Zr, and Sm, and enrichment in Cl, H₂O, F, and P in the primitive mantlenormalized patterns. The average normalized contents of moderately incompatible HREE in these magmas are close to those in the basic magmas of other geodynamic settings. Subduction basic magmas exhibit negative correlation of Li, Y, Dy, Er, Yb, Lu, and Ti contents with MgO content. Most of incompatible elements (Nb, Ta, U, Th, LREE) do not correlate with MgO, but correlate with each other and K₂O. Variations in element contents are related to crystallization differentiation, magma mixing, and possibly, participation of several sources. The water content in the island arc basic magmas varies from almost zero value to more than 6 wt %. Most compositions are characterized by weak negative correlation between H₂O and MgO contents, but some compositions define a negative correlation close to that in magmas of mid-ocean ridges (MOR). Considered magmas demonstrate distinct positive correlation between MgO content and homogenization temperature, practically coinciding with that of MOR magmas. Modeling of phase equilibria revealed widening of crystallization field of olivine in the magmas of subduction zones compared to MOR magmas. This can be related to the high water content in subduction magmas. Simultaneous liquidus crystallization of olivine and clinopyroxene in subduction magmas occurs at pressure approximately 5 kbar higher than that of MOR magmas. Based on the average ratios of trace element to K2O content, we determined the average compositions for subduction magma sources. Relative to depleted mantle, they are enriched in all incompatible elements, with positive anomalies of U, Rb, Ba, B, Pb, Cl, H₂O, F, and S, and negative anomalies of Th, K, Be, Nb, Ta, Li, Nd, Pb, and Ti. A general elevated content of incompatible elements indicates a reworking of the rocks of mantle wedge by fluids and melts that were released from the upper layers of subducted plate.     

Regional Variations in the Mineralogy of Metasomatic Assemblages in Mantle Xenoliths from the West Eifel Volcanic Field, Germany

Xenoliths record two distinct events in the mantle below theQuarternary West Eifel Volcanic Field, Germany. The first, duringthe Hercynian Orogeny, led to widespread formation of secondary,Ti-poor amphibole, clinopyroxene and phlogopite. The signatureof the second event, related to Quaternary volcanism, variesacross the field. At Dreiser Weiher and Meerfelder Maar, thisevent is characterized by amphibole–phlogopite–clinopyroxeneveins, hosted in lherzolite and harzburgite xenoliths broughtto the surface by sodic olivine nephelinite–basanite suitelavas. These veins formed from crystallization of sodic magmathat flowed along fractures in the mantle. At Rockeskyller Kopf,Gees and Baarley, the Quaternary event is characterized by wehrlitexenoliths, many of which have phlogopite–clinopyroxeneveins, that were transported by potassic foid suite lavas. Wehrliteformed by reaction of lherzolite–harzburgite, with a largevolume of potassic magma that flowed along grain boundariesrather than in fractures. During reaction, orthopyroxene wasconsumed and secondary clinopyroxene, olivine and phlogopiteprecipitated. Veins formed in wehrlites only during periodicover-pressure events. The composition of the magmas parentalto the veins is similar to the lavas that carried the xenolithsto surface, indicating that the source of foid and olivine nephelinite–basanitesuite magma is domainal, as was the flow regime and magma flux. KEY WORDS: Eifel; mantle xenoliths; metasomatism; trace elements     

Meimechites, porphyritic alkaline picrites, and melanephelinites of Siberia: Conditions of crystallization, parental magmas, and sources

The investigation of rocks, minerals, and melt inclusions showed that porphyritic alkaline picrites and meimechites crystallized from different parental magmas. At a similar ultrabasic composition, the alkaline picrite melts were enriched in K₂O relative to Na₂O, and contained up to 0.12–0.13 wt % F and less Cr, Ni, and H₂O (only 0.01–0.16 wt % H₂O, versus 0.6–1.6 wt % in the meimechite melts) compared with the meimechite magmas. The crystallization of alkaline picrite melts occurred under stable conditions at relatively low temperatures without abrupt changes: olivine and clinopyroxene crystallized at 1340–1285 and 1230–1200°C, respectively, as compared with 1600–1450 and 1230–1200°C in the meimechites. The alkaline picrite melts evolved toward melanephelinite, nephelinite, tephrite, and trachydolerite; whereas the meimechite magmas gave rise to subalkaline picritic rocks. The partitioning of vanadium between olivine and melt suggests that the meimechite magma crystallized under more oxidizing conditions compared with the alkaline picrite melts: the K_DV values for the meimechite melts (0.011–0.016) were three times lower than those for the alkaline picrite melts (0.045–0.052). The parental magmas of the alkaline picrites and meimechites were enriched in trace elements relative to mantle levels by factors of tens to hundreds. The alkaline picrite magma showed lower LILE and LREE contents compared with the meimechite magma. The magmas had also different indicator ratios of incompatible elements, including those immobile in aqueous fluids. It was concluded that the meimechite and alkaline picrite melts were derived from different mantle sources. The former were generated at lower degrees of melting of an undepleted mantle source, and the meimechite melts were produced by high-degree melting of a probably lherzolite-harzburgite source.     

Petrological and trace element geochemical features of the Okete Volcanics,western North Island,New Zealand

The Okete Volcanics form small volume monogenetic volcanoes situated around the flanks of larger tholeiitic cones of the Plio-Pleistocene Alexandra Volcanics, in the back-arc tectonic environment of western North Island, New Zealand. The lavas and tuffs of the Okete Volcanics have compositions which include basanites, alkali olivine basalts, olivine tholeiites, and hawaiites. Most rocks have Mg numbers >66, >250 p.p.m. Ni, >500 p.p.m. Cr, and often contain ultramafic xenoliths, which indicate that they are very close to being primary magmas. The Okete Volcanics show geochemical trends, from basanite to hawaiite, of progressive depletion of both compatible and incompatible trace elements, progressive increase in Al₂O₃, and heavy REE and Y enrichment with crossingover REE patterns in the hawaiites. These geochemical trends can be accounted for by varying degrees of partial melting of a light REE enriched garnet peridotite with subsequent modification of the melts near source or during ascent by fractional crystallization of olivine and minor clinopyroxene. Mass balance calculations cannot quantitatively constrain the degree of partial melting or fractional crystallization, but nevertheless indicate that the Okete alkali olivine basalts, olivine tholeiites, and hawaiites have been derived by successively larger degrees of partial melting relative to basanites, and have also been progressively more modified by fractional crystallization than have the basanites. Sources of the alkalic melts lay at depths corresponding to >20 kb, and most of the ultramafic xenoliths, apart from some which may be cognate cumulates, are unrelated to the magmas that brought them to the surface. Magmas have changed in composition with time from older smaller-volume volcanoes of basanite or alkali olivine basalt compositions, to younger and more voluminous volcanoes which contain hawaiites. The geochemical trends shown by the Okete Volcanics and their spatial association with voluminous tholeiitic volcanism, are features which are different from those observed elsewhere in the Pliocene to Recent basaltic fields of northern North Island, and may be related to their unique tectonic setting, situated in a distinct structural domain.     

Geochemistry of Neogene magmatism at Spitsbergen Island

Petrological and geochemical data obtained on Neogene magmatism restricted to a deep fault in Andree Land at Spitsbergen Island, which was related to the overall restyling of the Arctic territory at 25–20 Ma, indicate that the derivation of the Neogene magmas was significantly affected by the continental pyroxenite mantle. The Neogene basalts are noted for a radiogenic isotopic composition of Pb (²⁰⁷Pb/²⁰⁴Pb= 15.5–15.55, ²⁰⁶Pb/²⁰⁴Pb = 18.4–18.6, ²⁰⁸Pb/²⁰⁴ Pb = 38.4–38.6) and Sr(⁸⁷Sr/⁸⁶Sr = 0.7038–0.7048) at low ¹⁴³Nd/¹⁴⁴Nd = 0.5129. Melts of this type are the extremely enriched end member of the isotopic mixing of a depleted and enriched sources and determine a geochemical trend that passes through the compositions of alkaline magmas from Quaternary volcanoes at Spitsbergen and weakly enriched tholeiites of the Knipovich Ridge, which started to develop simultaneously with the onset of Neogene magmatism in the western part of Spitsbergen. The composition of the liquidus olivine (which is rich in NiO) indicates that melting occurred in the olivine-free mantle. Our data thus testify that a significant role in the genesis of the Neogene magmas was played by continental pyroxenite mantle.     

Origin and evolution of Neogene alkali-basaltic magmas in the southwestern flank of the Baikal rift system (Heven lava plateau,northern Mongolia)

The Heven lava plateau in the Hövsgöl field of the South-Baikal igneous province formed in the Early–Middle Miocene between 20 and 15.5 Ma. It consists of Early Miocene hawaiites and trachybasalts and Middle Miocene basanites erupted, correspondingly, during two major events in its history. The Heven alkali-basaltic lavas are compositionally similar to their counterparts from other volcanic fields in the southern flank of the Baikal rift system and are richer in Ba, K, Pb, and Sr than oceanic island basalts (OIB). The basanitic, hawaiitic, and trachybasaltic magmas were generated at pressures from 25 to 15 kbar and at temperatures in the range from 1434 to 1358 ºC. The magma sources occurred at 74 to 41 km in asthenospheric and lithospheric mantle and were ~200 ºC hotter than the ambient lithospheric mantle in the surrounding areas and the continental geotherm. The crystallization history of dark-colored began with liquidus highly magnesian olivine and Cr-spinel, and then several other parageneses formed successively as pressures and temperatures decreased: Ol + Cpx and Ol + Cpx + TiMgt ± Pl phenocrysts and subphenocrysts, Cpx + TiMgt + Ilm + Pl microphenocrysts, and finally interstitial Ne + Kfs alkali aluminosilicates. There were two crystallization stages with different mineral chemistry trends. The chemistry of minerals changed as the rising magmas first reached the crust–mantle region and then moved to shallow depths, erupted, and solidified. The generation of the Heven hawaiite–trachybasalt and basanite magmas was controlled by the depth of the reservoirs and the melt fraction in garnet-bearing asthenospheric and lithospheric mantle associated with progressive and regressive dynamics of the lower heterogeneous mantle plume consisting of PREMA and EMI components.     

The primary geochemistry of the monaro alkaline volcanics,southeastern Australia — evidence for upper mantle heterogeneity

The Mg numbers [100 Mg/(Mg+Fe) atomic ratios] of the Tertiary Monaro alkaline volcanics in southeastern Australia indicate that many of these alkali basalts, basanites and nephelinites have undergone only limited crystal fractionation, and that a few may represent unmodified, unfractionated primary magmas. Fractionation involves essentially olivine and clinopyroxene; fractionation trends are identified by plotting trace-element abundances against Mg number, and are then extrapolated linearly back into the primary magma field to yield estimates of the primary geochemistry of the three rock types.The nephelinites, basanites and alkali basalts are interpreted as a partial melting series derived from a peridotitic upper mantle. The estimated primary abundances of Pb,Th, Ga, V, Cr and Ni are essentially the same for the three rock types, but the estimated primary abundances of K₂O, Rb, Sr, Ba, TiO₂, Zr, Nb, P₂O₅, La Ce, Pr Nd, Y, Cu, and Zn-overlap considerably between the three rock types and the coherence of the incompatible elements as a group is not preserved in the overlaps. These patterns are best accounted for by postulating a patchy distribution of accessory phases such as amphibole, mica and apatite, in the source regions for the Monaro volcanics. Heterogeneities of this kind allow local variation in the volume of partial melt generated at the solidus, and offer a possible solution to magma segregation problems in the upper mantle.     

Eocene tonalite–granodiorite from the Havza (Samsun) area,northern Turkey: adakite-like melts of lithospheric mantle and crust generated in a post-collisional setting

ABSTRACT

Eocene intermediate to felsic plutons of different sizes and compositions are widespread in the Eastern Pontides Orogenic Belt in northern Turkey. Of these, the Ta?l?k Tepe pluton in the Havza (Samsun) area is fine-to-medium-grained, with granular, porphyritic, and micrographic textures, and include mafic microgranular enclaves (MMEs). LA-ICP-MS U-Pb zircon dating yielded emplacement ages of 42.9 (± 1.4) and 40.5 (± 1.3) Ma for the host granodioritic pluton and the dioritic MMEs, respectively. Petrochemically, the host pluton has I-type, high-K calc-alkaline, and metaluminous-to-slightly peraluminous features (A/CNK = 0.95–1.06). The host pluton also shows geochemical features of adakite-like rocks with high SiO₂ (67–68 wt%) and Al₂O₃ (15.5–16.0 wt%) content and Ba/La (17–23), Sr/Y (40.7–61.6), and La_N/Yb_N (14.4–23.7) ratios and low Y (8.2–9.9 ppm) and Yb_N (3.1–4.4) contents. Whole-rock major and trace element variations suggest that fractional crystallisation played a significant role in the pluton evolution. The N-MORB normalised trace element patterns of the pluton are similar to those of MMEs with enrichment in large-ion lithophile elements, Th and Ce, and negative Nb and Ti anomalies. Chondrite-normalised rare earth element plots show moderate-to-highly enriched concave patterns (La_N/Lu_N = 14.2–21.6) with insignificant negative Eu anomalies (Eu_N/Eu* = 0.86–1.14), all of which imply hornblende fractionation during magmatic evolution. The pluton samples have ⁸⁷Sr/⁸⁶Sr ratios of 0.704767 to 0.704927, ¹⁴³Nd/¹⁴⁴Nd ratios of 0.512767–0.512774, εNd values of (+2.52) – (+2.65), and δ¹⁸O values of 7.9–9.7‰. The isotopic compositions of the host pluton and MMEs are similar to I-type granitoids derived from mantle sources. The MMEs show incomplete magma mixing/mingling, representing small bodies of mafic parental magma. Combined with regional studies, these new data suggest that the parental magma of the studied adakite-like pluton was generated from the lithospheric mantle and then modified by fractional crystallisation and assimilation in a post-collisional setting.     

Petrogenesis of the Mesoproterozoic (1.23?Ga) Sudbury dyke swarm and its questionable relationship to plate separation

The Mesoproterozoic (~1.23 Ga) Sudbury dyke swarm was emplaced at equatorial latitudes and cross-cuts the Grenville, Southern and Superior Provinces of the Canadian Shield. The dyke swarm has been linked to the break-up of the Mesoproterozoic supercontinent Columbia (1.8 to 1.3 Ga). The Sudbury dykes are alkaline olivine diabases that extend ~300 km to the W and NW from the Grenville Front. Major element trends and MELTS modeling indicate fractional crystallization of olivine and plagioclase. Detailed mineral chemical analyses across a 90-m-wide dyke shows a symmetric M-shaped pattern indicating vertical flow differentiation. The highest measured Fo value of olivine from the chilled margin of one dyke is 70, suggesting the parental magmas of the dykes were evolved. Unlike other dykes of the Canadian Shield, the Sudbury dykes do not show significant chemical variation across the length of the swarm. The Sudbury dykes have high Sr/Y (>10), La/Yb_N (>5) and Sm/Yb_PM (>2.4) values indicating they originated from a garnet-bearing source. The low Th/Nb (<1.5) values contrast with the low Nb/La (<0.6) and La/Ba (~0.4) values, suggesting a possible lithospheric mantle or subduction-modified mantle source. In the context of Grenvillian tectonics, the Sudbury dykes intruded the Laurentian craton and parautochthonous rocks. The dykes occupy pre-existing west to northwest trending faults, suggesting that they exploited regional structural heterogeneities during the closure of the Elzevir basin (i.e., 1,250 to 1,190 Ma). The alkaline composition, limited spatial-chemical variation, volume, geometry and regional geological context suggest that the dykes are not likely related to a mantle plume or the break-up of a supercontinent.     

Mafic potassic lavas of the Quaternary West Eifel volcanic field

Major and trace element analyses for 103 volcanoes of the Quaternary West Eifel volcanic field show the lavas to be dominantly primitive (MgO>7 wt.%) and potassic (Na₂O/K₂O∼1). The rocks are divided into (1) a foidite (F)-suite, volumetrically dominant and consisting of four types: leucitites and nephelinites, melilite-bearing foidites, olivine-free foidites, sodalite-bearing melilite-free foidites, and (2) a younger olivine-nephelinite and basanite (ONB)-suite, concentrated in the southeastern part of the field. Dominantly cpx-phyric F-suite magmas differ from the dominantly ol-phyric ONB-suite mainly in higher K₂O/ Na₂O and CaO/Al₂O₃-ratios, higher Rb, Cu, H₂O, CO₂ and LREE concentrations and slightly lower Sr, Ni and Y contents. Most magmas have fractionated small amounts of olivine, clinopyroxene, and minor phlogopite. Systematic compositional variations within volcanoes or volcano groups are rare. Five more differentiated volcanoes (2 tephrites, 3 phonolites) occur in the center of the field. Their magmas are interpreted to have formed by fractionation within crustal magma chambers. Chemical differences between primary magmas (43% of volcanoes sampled) within both suites can be explained by different degrees of crystal fractionation at high pressures in the ascending magma column and possibly by varying degrees of partial melting (about 2–8%) in a garnetlherzolite mantle source. Distinct isotope ratios, parallel element variations, and different ratios of similarly incompatible elements, however, indicate a heterogeneous mantle beneath the West Eifel. The F-suite magmas originated from a mantle source more strongly enriched in alkalis and incompatible elements than the ONB-suite mantle source. The following model is proposed, based also on experimental studies and geophysical data: Within a large low velocity body of garnet-lherzolite, enriched in fluids and LIL elements (metasomatized mantle) between about 50 and 150 km depth, two different magma types were produced at different depths. Above a detachment level at about 50 km depth, these magmas rose to different stagnation levels or rapidly directly to the surface along vertical, dominantly NW-SE orientated fissures. The F-suite magmas probably formed in a phlogopite-bearing, CO₂-rich, strongly metasomatized source at about 100 km, the ON-Bmagmas from an amphibole-bearing, CO₂-poorer melting anomaly at about 60–75 km depth.