High-pressure inclusions in tholeiitic basalt and the range of lherzolite-bearing magmas in the Tasmanian volcanic province

Spinel-lherzolite xenoliths have been found in olivine tholeiite near Andover in the Tasmanian Tertiary volcanic province. They show a high-pressure mineralogy of predominant olivine (Mg₉₀), with aluminous enstatite (Mg₉₀) and lesser aluminous diopside and chrome-bearing spinel, and resemble lherzolite xenoliths commonly found in undersaturated lavas. Such xenoliths are unusual in tholeiitic basalts and the occurrence directly attests to a mantle origin for at least some tholeiitic magmas.The lherzolites are accompanied by doleritic and pyroxenitic xenoliths and by olivine, orthopyroxene, clinopyroxene and plagioclase xenocrysts. If near-liquidus phases are represented amongst the xenocrysts, then the magnesian number of the host basalt and its xenocryst assemblage provisionally suggest a magma derived by more than 15–20% partial melting of mantle peridotite, before commencing xenocryst crystallisation at pressures between 8–13 kbar.With this new record, lherzolite-bearing lavas in Tasmania now cover an extremely wide compositional range, extending from highly undersaturated olivine melilitite to olivine tholeiite. They also include a considerable number of fractionated alkaline rocks that are only sparsely reported in the literature as lherzolite hosts. This latter group contains representatives of a previously suggested but unestablished alkaline fractionation series based on olivine nephelinite, viz. calcic olivine nephelinite → sodic olivine nephelinite → potassi-sodic olivine nephelinite → mafic nepheline benmoreite → mafic phonolite.Lherzolite and megacryst-bearing lavas are relatively more abundant in peripheral parts to the main basalt sequences in Tasmania. This suggests that they developed in fringing zones of less intense mantle melting which enhanced stagnation and fractionation of magmas within the mantle before eruption. Calculated crustal thicknesses under these areas suggest that the magmas were generated at pressures exceeding 6–11 kbar, with the Andover tholeiitic magma exceeding 9 kbar.     

Origin of andesite and its bearing on the Island arc structure

The hypothesis that andesite magmas originate from basalt magmas through fractionation is supported for the following reasons: 1) A close association of andesite and dacite with basalt in many volcanoes and a complete gradation in chemistry and mineralogy throughout this suite. 2) Formation of andesite magmas from basalt magmas by differentiation in situ of some intrusive and extrusive bodies. 3) Agreement between the calculated compositions of solid materials to be subtracted from basalt magmas to yield andesite magmas and the observed mineralogy of phenocrysts in these rocks. 4) Higher alkali contents in andesite and dacite associated with high-alumina basalt than in those associated with tholeiite. 5) A complete gradation from the high iron concentration trend of basalt magma fractionation (Skaergaard) to the low or noniron concentration trend (the calc-alkali series) which can be ascribed to the difference of the stage of magnetite crystallization. 6) Similarity between the orogenic rock suite and plateau basalts in the preferential eruption of magmas of middle fractionation stage, givin rise to the great volume of andesite in the orogenic belts and iron-rich basalt in the plateau lavas. Petrological and seismic refraction studies suggest that a great volume of gabbroic materials are present in the lower crust underneath the volcanic belts as a complementary material for the andesite lavas. The island arc structure would develop by repeated eruption of andesite on the surface and by thickening of the oceanic crust underneath the arc due to the addition of gabbroic materials. The suitable portion of the lower crust may be subjected to partial melting to produce granitic magma in the later stage of development of the arc, successively changing it to a part of the adjacent continent.     

Mineralogy and chemistry of modern orogenic lavas — some statistics and implications

Island arc and continental margin (i.e. western Americas) lavas are divided (based on raw data from literature) into basalts (defined by absence of Ca-poor pyroxene, dominated by quartz-normative tholeiites); basaltic andesites and andesites (subdivided on basis of breaks in SiO₂ histogram and taken as <56% and 56–63% SiO₂; Ca-poor pyroxene present; amphibole and biotite absent); and hornblende (±biotite) lavas, which prove to be mainly relatively silicic andesites. Relative proportions of these types are (576 samples): 23% basalts, 29% basaltic andesites; 30% andesites; 18% hornblende andesites. The compilation emphasizes the dominance of calcic plagioclase (labradorite-anorthite) amongst the phenocryst phases. Pyroxenes are largely augite and hypersthene (En_60–75); olivine (Fo_65–85) is common through all compositions. There is an overall close similarity in chemistry and mineralogy between continental margin and island arc lavas, although small consistent differences are apparent (e.g. K₂O, TiO₂, P₂O₅).Modal data indicate that 70% of lavas are phenocryst-rich (20–60 vol.%), and that phenocryst contents show a bimodal distribution. Statistically and petrologically significant correlations are found between mineralogy and rock chemistry, most notably between total rock Al₂O₃ and modal phenocrystic plagioclase (found in all data groups, except hornblende andesites). This, and related data and correlations, indicate that the majority of orogenic magmas are modified by crystal fractionation (including crystal accumulation) processes dominated by plagioclase, and interpreted to occur under relatively low pressures. Dominance of plagioclase suggests phenocryst precipitation occurs typically in water-undersaturated magmas.     

Bimodal tholeiitic and mildly alkalic basalts from Bhir area,central Deccan Volcanic Province,India: Geochemistry and petrogenesis

Bimodal tholeiitic and mildly alkalic basalts occur near Bhir, in the central part of Deccan Volcanic Province (DVP). Major and trace element concentrations show that, of the ten flows, nine are tholeiitic and one is an alkalic basalt. The Bhir basalts have a wide range of chemical composition. Geochemical variations in the stratigraphic section define three distinct phases of evolution (zones 1 to 3). Crystal fractionation of plagioclase, clinopyroxene, olivine and Fe–Ti oxide expanded the compositional range. Low Mg#s (39–55), low concentrations of Ni and Cr and high Zr suggest the evolved nature of the Bhir basalts. Fractionation modeling suggests about 42% fractional crystallization.In spite of the dominant role of fractional crystallization in the evolution of Bhir basalts, some other processes must be sought to explain the chemical variations. Crustal contamination, magma mixing and degree of partial melting are suggested to explain the observed chemical variations. Resorption, reverse zoning and compositional bimodality in plagioclase phenocrysts indicate magma mixing. Samples of flows one and four suspected of being contaminated all have enriched SiO₂ and LILE (K, Rb, and Ba) contents and depletion in Ti and P, believed to be due to ‘granitic’ crustal contamination.As compared to tholeiitic basalts, the alkalic basalts are characterized by low SiO₂ and high TiO₂, Na₂O, K₂O and P₂O₅. Alkalic basalts are richer in LILE (Rb and Ba), HFSE (Nb, Zr, and Y) and REE than the tholeiitic basalts. The alkalic basalt occurrence is important from a petrogenetic point of view and also suggests that the sources of alkalic basalt magmas may be of variable ages under different parts of the DVP. Based on major, trace and rare earth element distributions it is suggested that asthenospheric mantle having affinities with the source of OIB was the source material of the magmas and the range in the composition of tholeiitic and alkalic basalts was probably controlled by different degrees of melting and/or inhomogeneities in the mantle source.     

Evidence for crustal assimilation by turbulently convecting,mafic alkaline magmas: Geochemistry of mantle xenolith-bearing lavas from northern Sardinia

Alkali basalt, trachybasalt and basanite magmas, containing abundant xenoliths of upper mantle origin, were erupted during the Plio-Pleistocene (2.4-0.14 Ma) in northern Sardinia. The magmas are enriched in K, Rb, Th and Ba relative to mid-ocean ridge basalts (MORB) and most ocean island basalts (OIB), resulting in high K/Nb, Th/Nb, Ba/Nb and Rb/Nb ratios. The large number of spinel peridotite inclusions in these lavas suggests that these chemical features cannot be explained by combined assimilation and fractional crystallization within the continental crust. However, volcanic rock chemistry can be explained by the assimilation of sialic rocks by turbulently convecting, mafic magmas during their ascent to the surface. Fractionation of Ba and K from the light rare earth elements (LREE) is required to explain the positive correlation of K/La and Ba/La with ⁸⁷Sr/⁸⁶Sr_(i). Consequently, bulk assimilation of crystalline basement rocks by rising, hot basaltic magmas cannot explain the observed chemical trends, and preferential melting of a low melting quartzo-feldspathic crustal component probably occurred, leaving the REE in residual phases such as apatite, zircon, sphene and amphibole. Alternatively, large ion lithophile element (LILE) enrichment may have been related to interaction of rising mafic lavas with metasomatized lithospheric mantle or enriched asthenosphere.     

On the lateral variations in chemical composition and volume of quaternary volcanic rocks across Japanese arcs

The Fe/Mg+Fe) ratios (X_Fe) of the Quaternary basalts (SiO₂ < 53 wt.%) in the Japanese arcs were examined. The X_XFe of relatively magnesian basalts decreases from the volcanic front toward the Japan Sea across the arcs. Based on the partition coefficient of Mg-Fe²⁺ between olivine and liquid, it is suggested that all the basalts near the volcanic front, which are mostly tholeiitic basalts, are significantly fractionated, whereas many basalts near the Japan Sea, which are mostly alkali basalts, are little fractionated. The K₂ O content in the primary basalt magmas increases toward the Japan Sea. Combining the X_Fe and K₂ O data, it is suggested that relatively large amounts of tholeiitic magmas are produced near the volcanic front, but they fractionate during their ascent, whereas smaller amounts of alkali basalt magmas are formed near the Japan Sea, but they can ascend with less fractionation. The density of primary tholeiite magma is significantly larger than that of primary alkali basalt magmas. It is most likely that primary tholeiite magmas cannot ascend beyond the upper crust and would fractionate to produce less dense tholeiitic magmas near the volcanic front, whereas primary alkali basalt magmas can ascend through the upper crust without fractionation, as far as buoyancy is the principal ascending force. In the Japanese arcs, the stress field may be less compressional near the Japan Sea than near the volcanic front, so that magmas can ascend more rapidly in the latter region than in the former. These two factors may be responsible for the above mentioned chemical variations of basalt magmas across the arcs. The variation in volume of the Quaternary volcanic rocks across the arcs can be explained by the presence of a melt-rich zone above but nearly parallel to the subducted slab.     

The petrochemistry of ophiolite gabbroic complexes. A key for the classification of ophiolites into low-Ti and high-Ti types

Ophiolites have been divided into two groups: high-Ti and low-Ti types. These can be discriminated by studying the fractionation trends of both gabbroic complexes (this work) and lavas and dykes [16], particularly in the TiO₂/M.I. diagram. The first type typically shows MORB-like magmas whereas in the second the magma types have a spectrum of composition from mid-ocean ridge basalts to island arc tholeiites and boninite-like magmas often occur.High-Ti ophiolites are petrologically and geochemically similar to major oceanic and ensialic back-arc basin crusts as well as oceanic crust generated during the intermediate and late-stage opening of intraoceanic back-arc basins.Parental magmas and fractionation processes of low-Ti ophiolites fit with an hypothesis of their formation in the early stage of opening of intraoceanic back-arc basins.     

Geochemistry and geochronology of Late Triassic volcanic rocks in the Chiang Khong region, northern Thailand

The Chiang Khong segment of the Chiang Khong–Lampang–Tak Volcanic Belt is composed of three broadly meridional sub‐belts of mafic to felsic volcanic, volcaniclastic, and associated intrusive rocks. Associated sedimentary rocks are largely non‐marine red beds and conglomerates. Three representative Chiang Khong lavas have Late Triassic (223–220 Ma) laser ablation inductively coupled mass‐spectroscopy U–Pb zircon ages. Felsic‐dominated sequences in the Chiang Khong Western and Central Sub‐belts are high‐K calc–alkaline rocks that range from basaltic to dominant felsic lavas with rare mafic dykes. The Western Sub‐belt lavas have slightly lower high field strength element contents at all fractionation levels than equivalent rocks from the Central Sub‐belt. In contrast, the Eastern Sub‐belt is dominated by mafic lavas and dykes with compositions transitional between E‐mid‐oceanic ridge basalt and back‐arc basin basalts. The Eastern Sub‐belt rocks have higher FeO* and TiO₂ and less light rare earth element enrichment than basalts in the high‐K sequences. Basaltic and doleritic dykes in the Western and Central sub‐belts match the composition of the Eastern Sub‐belt lavas and dykes. A recent geochemical study of the Chiang Khong rocks concluded that they were erupted in a continental margin volcanic arc setting. However, based on the dominance of felsic lavas and the mainly non‐marine associated sediments, we propose an alternative origin, in a post‐collisional extensional setting. A major late Middle to early Late Triassic collisional orogenic event is well documented in northern Thailand and Yunnan. We believe that the paucity of radiometric dates for arc‐like lavas in the Chiang Khong–Lampang–Tak Volcanic Belt that precede this orogenic event, coupled with the geochemistry of the Chiang Khong rocks, and strong compositional analogies with other post‐collisional magmatic suites, are features that are more typical of volcanic belts formed in a rapidly evolving post‐collisional, basin‐and range‐type extensional setting.     

The Zealandia Volcanic Complex: Further evidence of a lower crustal “hot zone” beneath the Mariana Intra‐oceanic Arc,Western Pacific

This paper addresses formation of felsic magmas in an intra‐oceanic magmatic arc. New bathymetric, petrologic, geochemical, and isotopic data for Zealandia Bank and two related volcanoes in the south‐central Mariana arc is presented and interpreted. These three volcanoes are remnants of an older andesitic volcano that evolved for some time and became dormant long enough for a carbonate platform to grow on its summit before reawakening as a rhyodacitic volcano. Zealandia lavas are transitional between low‐ and medium‐K and tholeiitic and calc‐alkaline suites. They define a bimodal suite with a gap of 56–58 wt% SiO₂; this suggests that mafic and felsic magmas have different origins. The magmatic system is powered by mantle‐derived basalts having low Zr/Y and flat rare earth element patterns. Two‐pyroxene thermometry yields equilibration temperatures of 1000–1100 °C for andesites and 900–1000 °C for dacites. Porphyritic basalts and andesites show textures expected for fractionating magmas but mostly fine‐grained felsic lavas do not. All lavas show trace element signatures expected for mantle and crustal sources that were strongly melt‐depleted and enriched by subduction‐related fluids and sediment melts. Sr and Nd isotopic compositions fall in the normal range of Mariana arc lavas. Felsic lavas show petrographic evidence of mixing with mafic magma. Zealandia Bank felsic magmatism supports the idea that a large mid‐ to lower‐crustal felsic magma body exists beneath the south‐central Mariana arc, indicating that MASH (mixing, assimilation, storage, and homogenization) zones can form beneath intra‐oceanic as well as continental arcs.     

The Hasan Dagi stratovolcano (Central Anatolia, Turkey): evolution from calc-alkaline to alkaline magmatism in a collision zone

The Hasan Dagi volcano is one of the two large Plio-Quaternary volcanoes in Cappadocia (Central Anatolia, Turkey). Three stages of edifice construction have been identified for this volcano: Paleovolcano, Mesovolcano and Neovolcano. Most samples from Hasan Dagi volcano are calc-alkaline and define an almost complete trend from basaltic andesite to rhyolite. However, the more recent (Neovolcano) mafic samples are alkaline basalts. The mineralogical and geochemical characteristics of the oldest lavas (Keçikalesi (13 Ma) and Paleo-Hasan Dagi (7 Ma)) are significantly different from those of the younger lavas (Meso- and Neo-Hasan Dagi (<1 Ma)). Calcic plagioclase and pigeonite are typically observed in these older lavas. The Paleovolcano basalts are depleted in alkalis and display a tholeiitic tendency whereas the differentiated lavas are depleted in Na₂O but enriched in K₂O compared to younger lavas. There is an evolution through time towards higher TiO₂, Fe₂O₃^*, MgO, Na₂O and K₂O and lower Al₂O₃ and SiO₂ which is reflected in the basalt compositions. All the basalts display multi-element patterns typical of continental margin magmas with a significant enrichment in LILE (K, Rb, Ba and Th) and LREE and strong (Paleovolcano) to moderate (Meso- and Neovolcano) negative Nb, Zr and Ti anomalies. However, the younger basalts are the most enriched in incompatible elements, in agreement with their alkaline affinities and do not systematically display negative HFSE anomalies. REE data suggest an hydrous amphibole-bearing crystallization history for both Meso- and Neovolcano lavas. The distinction between the older and younger lavas is also apparent in trace element ratios such as Nb/Y, Ti/Y and Th/Y. These ratios indicate the role of a subducted component±crustal contamination in the genesis of the Hasan Dagi lavas, particularly for the oldest lavas (Keçikalesi and Paleo-Hasan Dagi). The decreasing influence of this component through time, over the last 6–7 m.y., has been accompanied by an increasing contribution of melt-enriched lithosphere. Although the range of variation of Sr, Nd and Pb isotopic ratios is small (0.70457–0.70515; 0.51262–0.51273; 18.80–18.94; 15.64–15.69; 38.87–39.10), it also reflects the evolution of the magma sources through time. Indeed, the youngest (Neovolcano) and most primitive basalts display significantly lower ⁸⁷Sr/⁸⁶Sr than the Paleo- and Mesovolcano basalts, whereas the Mesovolcano basalts display more radiogenic Pb than Paleovolcano samples. Magma mixing processes between initially heterogeneous and/or variably contaminated magmas may account for the genesis of the less differentiated and intermediate lavas (48–57% SiO₂). Meso- and Neovolcano differentiated lavas (60–68% SiO₂) are either derived from the analyzed basalts or from more primitive and more depleted magmas by fractional crystallization±some crustal contamination (AFC). Furthermore, the highly differentiated samples (72–75% SiO₂) are not strongly contaminated. The strong calc-alkaline character of Hasan Dagi lavas, in the absence of contemporaneous subduction, must reflect the heritage of the early subduction of the Afro–Arabian plate under the Eurasian plate. The evolution towards alkaline compositions through time is clearly related to the development of extensional tectonics in Central Anatolia in the Late Miocene.     

Subdivision of the Archean lavas of the Abitibi area,Canada, from Fe-Mg-Ni-Cr relations

The lavas of a part of the Archean Abitibi region may be divided into three stratigraphic levels in each of which FeO-MgO-Ni-Cr contents conform to certain broad differentiation trends. Within each stratigraphic level, there is a tendency for rocks to become more felsic upwards. The earliest and stratigraphically lowest subdivision is composed largely of magnesium-rich basaltic lavas called the magnesian suite. In the central part of the pile, where basalts predominate, the lavas contain intermediate MgO concentrations, and display pronounced Fe enrichment in intermediate members similar to conventional tholeiites. In the latest and stratigraphically highest lavas, where andesites predominate, Fe depletion is characteristic; these lavas are grouped into a primitive calcalkaline suite. All of the Abitibi lavas contain unusually high Ni and Cr. Other Archean lava piles appear to be similarly divisible, although all three suites are not always present.Mafic end-members of the three complete differentiation suites are viewed as possible source magmas derived by partial melting in a primitive, olivine-rich parent, probably the Archean mantle. The earliest, and highest temperature magmas precipitated olivine, Al-clinopyroxene, and minor Al-orthopyroxene, and display moderate FeO, TiO₂, MnO, Al₂O₃, and CaO enrichment in more felsic members. The intermediate age lavas, derived originally by less complete melting in the parent, precipitated plagioclase, olivine, and lesser clinopyroxene, and display, as a result, strong Fe enrichment until, in intermediate members, magma volumes became small enough to yield P_f of levels sufficient to form clinopyroxene plus magnetite. The uppermost lavas, derived by relatively small volumetric melting in the parent, contain abundant Fe-Ti oxides in even the most mafic members, along with augite and plagioclase.     

Content and behavior of fluorine in Japanese quaternary volcanic rocks and petrogenetic application

Fluorine contents in about 160 representative Quaternary volcanic rocks and 15 hornblende and biotite phenocrysts in a calc-alkali series in Japan have been determined by a selective ion-electrode method. Tholeiites have the lowest contents and the narrowest range (58–145 ppm), while alkali basalts have the highest contentws and the widest range (301–666 ppm), high-alumina basalts have intermediate values (188–292 ppm). F contents in basalts clearly increase from east to west across the Japanese Islands, as do alkalies, P₂O₅ REE, U, Th and H₂O.The volcanic rocks studied are divided into two groups on the basis of F: (1) witt, increasing % SiO₂ or advancing fractionation, F contents show either progressive enrichment; or (2) with increasing fractionation, F contents show rather constant values. The former is produced by fractionation of anhydrous phases from basalt to mafic andesite magmas; the tholeiite series of Nasu volcanic zone (outer zone), northeastern, Japan is a typical example. The latter group is derived through separation of amphibole-bearing phases from basaltic magmas at various depths from upper mantle (about 30 km) to upper crust; the alkali series in southwestern Japan and the calc-alkali series of Chokai volcanic zone (inner zone), northeastern Japan, are examples.     

Fractionation trends of basalt magmas in lava flows

Chemical compositions of schlieren in basalt flows are compared with those of the host rocks for tracing the fractionation trends of basalt magmas under extrusive conditions. In the Warner high-alumina basalt of California and in the tholeiite of Hawaii and Japan, total iron increases markedly from the host rock to the schlieren whileSiO ₂ is nearly constant. In the high-alumina basalt of Huzi Volcano and in the tholeiite near Catania, Italy, total iron is nearly constant during fractionation whileSiO ₂ increases. In basalts of the hypersthenic rock series or calc-alkali rock series from California, total iron is also nearly constant whileSiO ₂ increases. The difference in fractionation trend in these flows is attributable to the difference of the state of oxidation of iron in the original magmas. Oxygen partial pressure of the magmas would not be maintained constant during the fractionation of extrusive bodies.     

The petrology, phase relations and tectonic setting of basalts from the taupo volcanic zone, New Zealand and the Kermadec Island arc - havre trough, SW Pacific

Volcanism in the Taupo Volcanic Zone (TVZ) and the Kermadec arc-Havre Trough (KAHT) is related to westward subduction of the Pacific Plate beneath the Indo-Australian Plate. The tectonic setting of the TVZ is continental whereas in KAHT it is oceanic and in these two settings the relative volumes of basalt differ markedly. In TVZ, basalts form a minor proportion (< 1%) of a dominant rhyolite (97%)-andesite association while in KAHT, basalts and basaltic andesites are the major rock types. Neither the convergence rate between the Pacific and Indo-Australian Plates nor the extension rates in the back-arc region or the dip of the Pacific Plate Wadati-Benioff zone differ appreciably between the oceanic and continental segments. The distance between the volcanic front and the axis of the back-arc basin decreases from the Kermadec arc to TVZ and the distance between trench and volcanic front increases from around 200 km in the Kermadec arc to 280 km in TVZ. These factors may prove significant in determining the extent to which arc and backarc volcanism in subduction settings are coupled.All basalts from the Kermadec arc are porphyritic (up to 60% phenocrysts) with assemblages generally dominated by plagioclase but with olivine, clinopyroxene and orthopyroxene. A single dredge sample from the Havre Trough back arc contains olivine and plagioclase microphenocrysts in glassy pillow rind and is mildly alkaline (< 1% normative nepheline) contrasting with the tholeiitic nature of the other basalts. Basalts from the TVZ contain phenocryst assemblages of olivine + plagioclase ± clinopyroxene; orthopyroxene phenocrysts occur only in the most evolved basalts and basaltic andesites from both TVZ and the Kermadec Arc.Sparsely porphyritic primitive compositions (Mg/(Mg+Fe²) > 70) are high in Al₂O₃ (>16.5%), and project in the olivine volume of the basalt tetrahedron. They contain olivine (Fo₈₇) phenocrysts and plagioclase (> An₆₀) microphenocrysts. These magmas have ratios of CaO/Al₂O₃, A1₂O₃/TiO₂ and CaO/TiO₂ in the range of MORB and MORB picrites and can evolve to the low-pressure MORB cotectic by crystallisation of olivine±plagiociase. Such rocks may be the parents of other magmas whose evolutionary pathways are complicated by interaction of crystal fractionation, crystal accumulation and mixing processes and the filtering action of crust of variable density and thickness. The interplay of these processes likely accounts for the scatter of data about the cotectic. More evolved rocks from both TVZ and KAHT contain clinopyroxene and orthopyroxene phenocrysts and their compositions merge with basaltic andesites and andesites. Stepwise least-squares modelling using phenocryst assemblages in proportions observed in the rocks suggest that crystal fractionation and accumulation processes can account for much of the diversity observed in the major-element compositions of all lavas.We conclude that the parental basaltic magmas for volcanism in the TVZ and KAHT segments are similar thereby implying grossly similar source mineralogy. We attribute the diversity to secondary processes influencing liquids as they ascended through complex plumbing systems in the sub arc mantle and cross.     

Petrology and geochemistry of alkali basalts and ultramafic inclusions from the palei-aike volcanic field in Southern Chile and the origin of the patagonian plateau lavas

The Palei-Aike volcanic field, the southernmost unit of the Patagonian plateau lavas, consists of Pleistocene to Recent alkali olivine basalts petrologically and geochemically similar to alkali basalts from diverse tectonic environments. The Palei-Aike basalts have lower SiO₂ and Al₂O₃ and higher TiO₂ and P₂O₃ than published analyses of other Patagonian plateau basalts. Garnet, garnet + spinel-, and phlogopite-peridotites, not reported from other Patagonian plateau lavas or from elsewhere in South America, are common inclusions within Palei-Aike lavas along with spinel-lherzolite, dunite, granulites, and aluminous clinopyroxene megacrysts. The inclusion of these high-pressure assemblages indicates a mantle origin for the Palei-Aike lavas. The Patagonian plateau lavas are located in a tectonic position similar to back-arc basins, and their origin may be a consequence of subduction. The origin and distinct chemical features of the Palei-Aike basalts may be due in part to thermal or mechanical perturbations of the mantle related to changes in plate boundaries and motions in the vicinity of the unstable trench-transform triple junction formed by the South American, Antarctic and Scotia plates.     

The transition from calc-alkaline to potassic orogenic magmatism in the Aeolian Islands,Southern Italy

The Aeolian volcanic arc displays a wide range of magmatic products. Mafic lavas range from hypersthene normative calc-alkaline basalts to silica-undersaturated potassic absarokites, although the former are spatially and temporally dominant, consistent with the subduction-zone tectonic setting. In addition, intermediate and acidic members of the various fractionation series may be recognised. Large variations in trace element and isotope ratios accompany the rapid calc-alkaline to potassic transition, and it is argued that these may be largely explained in terms of subduction-zone mantle enrichment involving components derived from both basaltic ocean crust and subducted sediments. In addition, it seems that the mantle wedge itself was substantially heterogeneous prior to the onset of subduction zone processes. Not only are these subduction components similar to those proposed in a number of island arcs, but they also resemble those recognised in the ultra-potassic lavas of the Roman province, supporting recent subduction-related petrogenetic models of the Roman magmatism. Although subducted sediment plays an important role in the generation of some potassic magmatism, it is not uniquely responsible for K₂O-rich lavas, which are also produced without a large sediment contribution.     

Open-system processes in the genesis of silica-oversaturated alkaline rocks of the Rallier-du-Baty Peninsula, Kerguelen Archipelago (Indian Ocean)

The Rallier-du-Baty Peninsula forms the southwestern part of the Kerguelen Archipelago (Indian Ocean), whose magmatic activity is related to the long-lived 115-Ma Kerguelen plume. The peninsula is mostly made of alkaline rocks constituting two well-defined ring complexes. This paper focuses on the northern ring complex, which is not yet known. Recent field studies have revealed seven discrete syenitic ring dykes ranging in age from 6.2 to 4.9 Ma, and two later volcanic systems. ⁴⁰Ar/³⁹Ar dating of a trachytic ignimbrite linked to the Dôme Carva volcano complex yields an age of 26±3 Ka. This represents the last major eruptive event on the Kerguelen Archipelago. The volcanism is bimodal with trachybasalts and trachyandesites constituting the mafic lavas and trachytes and rhyolites constituting the felsic lavas. The volume of erupted felsic magma is by far the larger, and is represented by abundant pyroclastic deposits and lava flows. Boulders of plutonic rocks are found to the northwest of Dôme Carva, and represent intermediate rocks (i.e. monzogabbros and monzonites) that are not present at the surface. Basic rocks are mostly trachybasalts and trachyandesites, while true basalts are scarce. Their mineralogy consists chiefly of plagioclase, olivine, diopside and oxides. Sieve-textured plagioclase is common, as well as corroded olivine and diopside phenocrysts. Peralkaline commenditic trachytes are the most abundant type of acid volcanic rocks. They consist of abundant sanidine, augite and magnetite phenocrysts and interstitial quartz, aegerinic pyroxenes and Na-amphiboles. Ring dykes of quartz-poor alkali feldspar syenites display the same mineralogy, except hornblende is common and replaces diopside. Hornblende is particularly abundant in intermediate monzogabbros. Major and trace element variations of volcanic rocks emphasise the predominant role of fractional crystallisation with a general decrease of MgO, CaO, P₂O₅, TiO₂, FeO, Ba, Sr and Ni from basic to felsic rocks. However, the scattering of the data from the basic rocks indicates that other processes have operated. The overall evolution from trachyte to rhyolite is in agreement with the fractionation of sanidine as the major control. An increase of incompatible elements from trachyte to rhyolite is observed. The felsic lavas display an increase of ⁸⁷Sr/⁸⁶Sr_(i) without any significant variations in the Nd isotopic composition. The genesis of the basic rocks is complex and reflects concomitant processes of fractional crystallisation, mixing between different basic magmas and probable assimilation of Ba-rich oceanic crust. Major and trace element modelling confirms the possibility of producing the trachytes through continuous differentiation from a basaltic alkaline parent. Discrepancies observed for some trace elements can be explained by the crystallisation of amphibole at an intermediate stage of magma evolution. The overall evolution from trachyte to rhyolite is thought to be controlled by crystal fractionation. High ⁸⁷Sr/⁸⁶Sr_(i) of the trachytes is interpreted to reflect interaction with an ocean-derived component, probably during assimilation of hydrothermally altered oceanic crust. Boulders of amphibole-bearing monzonites and monzogabbros found to the northwest of Dôme Carva are thought to represent intermediate magma composition that formed at depths but did not erupt.     

Bimodal volcanism at the Katla subglacial caldera,Iceland: insight into the geochemistry and petrogenesis of rhyolitic magmas

The Katla subglacial caldera is one of the most active and hazardous volcanic centres in Iceland as revealed by its historical volcanic activity and recent seismic unrest and magma accumulation. A petrologic and geochemical study was carried out on a suite of mid-Pleistocene to Recent lavas and pyroclastic rocks originated from the caldera. The whole series is characterised by a bimodal composition, including Fe-Ti transitional alkali basalts and mildly alkalic rhyolites. Variations in trace-element composition amongst the basalts and rhyolites show that their chemical differentiation was mainly controlled by fractional crystallisation and possible assimilation. The petrology and chemistry of the few intermediate extrusive rocks show that they were derived from magma mingling or hybridisation. The absence of extrusive rocks of true intermediate magmatic composition and the occurrence of amphibole-bearing felsic xenoliths support the hypothesis of partial melting of the hydrated basalt crust as the main process leading to the generation of rhyolites. The ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr values of Katla volcanic rocks fit the general isotopic array defined by late Quaternary to Recent lavas from Iceland. A few rock specimens are distinguished by low ¹⁴³Nd/¹⁴⁴Nd values suggesting assimilation and mixing of much older crustal material. Despite their similar whole-rock chemical compositions, the postglacial rhyolitic extrusives differ from the felsic xenoliths by their glass composition and the absence of amphibole. This, together with the general chemical trend of volcanic glasses, indicates that the postglacial rhyolitic extrusives were probably derived by a process involving late reheating and partial melting of crustal material by intrusion of basaltic magmas.     

The origin of intermediate and evolved lavas in the Marquesas archipelago: an example from Nuku Hiva island (French Polynesia)

The Nuku Hiva Pliocene island (Marquesas, French Polynesia) is composed of a large half-collapsed tholeiitic shield volcano (the Tekao edifice), the caldera of which is filled up by the younger Taiohae volcano. The latter edifice is characterised by a complex magmatic association including minor mafic lavas (olivine tholeiites, alkali basalts and basanites), abundant intermediate lavas (hawaiites with subsidiary mugearites, both covering 47% of the surface of the volcano) and lesser amount of evolved lavas (K-rich and Na-rich trachytes and minor benmoreites, covering 25% of the edifice). Most intermediate and evolved Taiohae lavas are amphibole-rich and crystallised under high oxygen fugacities. The mafic Taiohae lavas originated from lower degree of melting of mantle sources more enriched than that of the shield volcano tholeiites. We show that closed-system fractional crystallisation of the Taiohae basaltic magmas can account for the origin of Taiohae hawaiites and mugearites, provided that separation of substantial amount of amphibole and/or apatite occurred during this process. Similarly, fractionation of benmoreitic magmas involving large amounts of amphibole and mica may account for the genesis of K-rich and Na-rich trachytes, respectively. However, fractional crystallisation cannot account for the derivation of benmoreitic magmas from mugearitic ones: since, this process fails to explain the abrupt increase in K₂O from the latter to the former. In addition, the isotopic signature of trachytes and benmoreites is clearly distinct (more EM II-rich) from that of Taiohae basalts, hawaiites and mugearites. Three hypotheses could account for the genesis of benmoreitic magmas: assimilation of oceanic material with a strong EM II signature, differentiation of non-sampled mafic magmas derived from a mantle source having a EM II-rich signature and partial melting at depth of mafic material with a strong EM II signature. The oxidised character of Nuku Hiva lavas, uncommon in oceanic island settings, suggests interaction with water and/or the contribution of an oxidised (altered?) source material to their genesis.     

Flux versus decompression melting at stratovolcanoes in southeastern Guatemala

The major and trace element geochemistry of lavas erupted from four volcanic front (VF) stratovolcanoes in southeastern Guatemala show differences in the relative importance of flux and decompression melting in a continental arc setting. The VF stratovolcanoes exhibit a wide compositional range from basalt to dacite, although modern Pacaya erupts basaltic lavas. The VF basalts have relatively low MgO contents and plot outside the field of primary arc magmas defined by melting experiments on hydrous peridotite. After subtracting the effects of the fractionation, assimilation, and alteration of some VF lavas, separate partial melting and mixing trends were identified for Agua–Pacaya and Tecuamburro–Moyuta.The distinct chemical signatures of the hemipelagic and carbonate sediments subducted off Guatemala provide constraints on material transfer processes that occurred between the slab and mantle wedge. Model fluids and melts from the subducted slab were calculated using recently published mineral–aqueous fluid partition coefficients. Wide separation of the model fluid and melt compositions on a U/La versus Ba/Th diagram creates diagnostic mixing curves with an enriched mid-ocean ridge basalt source. Fluid from mature ocean crust has high U/La, fluid from carbonate sediment has high Ba/Th, and fluid and melt from hemipelagic sediments have both high U/La and Ba/Th. In a simple single-stage model, a mantle metasomatized by fluid originating largely from the oceanic crust with only minor sediment fluid contributions best explains the overall large ion lithophile element composition of the VF lavas. (Th/Rb)_N ratios of ∼1 in the VF lavas from southeastern Guatemala require a component of sediment melting. Therefore, a more realistic two-stage model to describe the Guatemalan arc data involves an initial hemipelagic sediment melt input to the wedge followed by minor fluid additions from the oceanic crust or sediments. Correlation between measures of slab input and extent of melting in the older VF lavas from Tecuamburro and Moyuta favors flux-dominated melting near the base of the mantle wedge. In sharp contrast, the lack of a relationship between slab additions and melting in younger lavas from Agua and Pacaya volcanoes implies a significant role for decompression melting closer to the top of the wedge. In this melting scenario, the rate of crustal extension determines the extent of melting.