Melting experiments on a high-magnesian andesite

Melting experiments were conducted on a high-magnesian bronzite olivine andesite (Teraga-Ike andesite) which is considered to be a primary andesite. The high-magnesian andesite magma is in equilibrium with both olivine and orthopyroxene at about 15.5 kbar and 1080°C under H₂O-saturated conditions and at lower pressure and higher temperature under H₂O-undersaturated conditions. This suggests that high-magnesian andesites could be generated by the partial melting of upper mantle peridotite containing a small amount of H₂O.     

Geochemical and petrological constraints on rear-arc magma genesis processes in Ecuador: The Puyo cones and Mera lavas volcanic formations

The Puyo scoria cones and the Mera lava flows, two newly recognized volcanic formations dated between Late Pliocene to Middle Pleistocene, extend the limits of the Ecuadorian rear-arc volcanic province some 100 km to the south. The Puyo scoria cones have erupted K-rich absarokites containing olivine, diopside and phlogopite, whereas the Mera lava flows display a basic andesite composition, with olivine and minor augite phenocrysts. In addition to high contents in LILE, LREE and HFSE, the Puyo absarokites exhibit many characteristics of primitive melts, namely high Cr (590–310 ppm) and Ni (330–154 ppm) contents, high Mg# (64–70) and they contain forsteritic olivine (Fo_82–89). The composition of the most primary Puyo absarokite was used in petrogenetic models, in order to constrain the genesis of these high-K magmas. Major and trace elements models, as well as isotopic data, indicate that the source of Puyo magmas is a hydrated phlogopite- and garnet-bearing lherzolite. Phlogopite crystallization in the mantle wedge is triggered by the metasomatism by 3–5% of a SiO₂-, H₂O-rich liquid generated by slab melting. Partial melting of the subducted oceanic crust beneath Ecuador is allowed by the subduction of the young and warm Carnegie Ridge, which modifies the thermal regime of the Benioff zone. A low degree (1–4%) of partial melting of the metasomatized mantle wedge, leaving a variable garnet (4–7%) ± phlogopite (0–4%) lherzolitic residual assemblage, leads to the compositions of the entire Puyo absarokite series and is consistent with previous petrogenetic models developed for the Ecuadorian volcanic arc. Indeed, the homogeneity of isotopic data across the arc suggests a similar source for the whole Ecuadorian magmas.     

Origin of high-magnesian andesites in the Setouchi volcanic belt,southwest Japan,I. Petrographical and chemical characteristics

High-magnesian andesites of middle Miocene age occur in southwest Japan, forming an obvious volcanic belt. These andesites have low FeO*/MgO ratios (0.546–0.931), and are rich in Ni (101–312 ppm), Co (30.0–45.1 ppm), and Cr (208–756 ppm). They are relatively aphyric (phenocrysts <10 vol.%), and the phenocrysts of magnesian olivine (～Fo₈₈) are in equilibrium with the host high-magnesian andesite magmas on the basis of the Fe-Mg exchange partitioning. These features suggest that the high-magnesian andesites are not differentiated or accumulative; they appear to represent primary andesites generated in the upper mantle. These southwest Japanese high-magnesian andesites are rich in incompatible elements, and show light rare earth enrichment relative to boninites, suggesting that the former is derived from a less depleted mantle source than the latter.     

High-magnesium primary magmas from Haleakala Volcano, east Maui, Hawaii: petrography, nickel, and major-element constraints

For any given volcanic field the compositions of primary melts provide important constraints on models of magmatic processes and volcanic eruptions. In this paper, based on petrography, olivine and bulk rock compositions, two tholeiitic picrites (samples C122 and C123) from Haleakala Volcano, east Maui are evaluated as possible primary melts. Sample C122 (bulk rock MgO = 16.6%) has a high apparent Mg-Fe exchange coefficient, K_D, between olivine phenocrysts and bulk rock (0.6). However, major-elements and Ni mass-balance calculations show that the olivines in C122 are in equilibrium with the residual melt (matrix) after closed-system equilibrium fractionation of 25 wt.% olivine. Therefore, the Mg/Fe ratio, Ca content, and Ni content of C122 are consistent with the hypothesis that the bulk composition of C122 is close to a primary melt formed by partial melting of a mantle containing olivine with composition around Fo₈₉ to Fo₉₁. The uniform composition and small size (mostly 0.2–0.3 mm) of the olivine, and the glass patches in the matrix suggest fast ascent, and rapid cooling at shallow depth for C122. On the contrary, sample C123, which has an apparent K_D (between the most mafic olivine megacrysts and the bulk rock) close to the equilibrium value (0.27), the multiple planar subgrain boundaries in most of the olivine crystals indicate that it may not be a primary melt unless the deformed olivines are generated at magmatic condition as phenocrysts. If the deformed subgrain boundary texture in olivine could indeed be generated at magmatic condition, then the wide compositional range of olivine crystals in C123 (Fo₇₄ to Fo₉₁) suggests multi-stage crystallization over a wide range of cooling temperatures.The compositions of the two picrites, and a differentiated basalt which does not contain xenocrysts suggest that the Haleakala tholeiites are derived from primary melts with at least 16–17 wt.% MgO. Lavas with such high MgO content are rare in Haleakala and other Hawaiian volcanoes; therefore, most Hawaiian tholeiites must have undergone extensive fractionation histories.     

Evidence of magma mixing: Petrological study of Shirouma-Oike calc-alkaline andesite volcano, Japan

Shirouma-Oike volcano, a Quaternary composite volcano in central Japan, consists mostly of calc-alkaline andesitic lavas and pyroclastic rocks. Products of the earlier stage of the volcano (older group) are augite-hypersthene andesite. Hornblende crystallized during the later stage of this older group, whereas biotite and quartz crystallized in the younger group.Assemblages of phenocrysts in disequilibrium, such as magnesian olivine(Fo₃₀)/quartz, iron-rich hypersthene(En₅₅)/iron-poor augite(Wo_43.5, En_42.5, Fs_14.0), and two different types of zoning on the rim of clinopyroxene are found in a number of rocks. Detailed microprobe analyses of coexisting minerals reveal that phenocrysts belong to two distinctly different groups; one group includes magnesian olivine + augite which crystallized from a relatively high-temperature (above 1000°C) basaltic magma; the second group, which crystallized from relatively low temperature (about 800°C) dacitic to andesitic magma, includes hypersthene + hornblende + biotite + quartz + plagioclase + titanomagnetite ± ilmenite (in the younger group) and hypersthene + augite + plagioclase + titanomagnetite ± hornblende (in the older group). The temperature difference between the two magmas is clarified by Mg/Fe partition between clinopyroxene and olivine, and Fe-Ti oxides geothermometer. The compositional zoning of minerals, such as normal zoning of olivine and magnesian clinopyroxene, and reverse zoning of orthopyroxene, indicate that the basaltic and dacitic-andesitic magmas were probably mixed in a magma reservoir immediately before eruption. It is suggested that the basaltic magma was supplied intermittently from a deeper part to the shallower magma reservoir, in in which dacitic-andesitic magma had been fractionating.     

Mineralogical and geochemical evolution of the 1982–1983 Galunggung eruption (Indonesia)

Pyroclastic deposits from the 1982–1983 eruption of Galunggung volcano (Java, Indonesia) reflect preeruptive magmatic evolution which is of interest because of: (1) its duration of nine months, compared to a few hours or days for most historical eruptions; (2) the diversity of eruptive styles, from ash and scoria flows to phreatomagmatic explosions, and to the strombolian activity that marked the end of the eruption; and (3) the progressive variation in chemical composition with time, from andesite (58 wt.% SiO₂) to high-Mg basalt (47 wt.% SiO₂). The 1982–1983 Galunggung basalts are rather primitive: 10 to 12 wt% MgO, 180 to 200 ppm Ni and 550 to 700 ppm Cr. Despite the presence of about 40% phenocrysts, they may represent the most primitive basalts recognized in western Java. Basalts contain phenocrysts of olivine (Fo_90-80), diopside-salite, and plagioclase (An_95-75). Andesites contain plagioclase (An_80–60), augite, hypersthene (En_67-64), and titanomagnetite. The distribution of mineral compositions in each petrographic type is nearly unimodal, although scarce plagioclase and olivine xenocrysts have been observed. Abundance of gabbroic cumulates associated with the pyroclastic flows and evolution of mineral compositions from high-Mg basalts to andesites support crystal fractionation as the main differentiation mechanism, although magma mixing of basaltic andesite and andesite cannot be excluded. Major and trace element trends, which display rough decreases of MgO, CaO, Ni, Cr with increasing degree of differentiation and also linear positive correlations of hygromagmaphile elements, are compatible with both processes. However, some discrepancies are observed between major and trace element modelling, which may be explained to some extent by the influence of in situ crystallization and/or magma mixing. The constancy of ¹⁴³Nd/¹⁴⁴Nd (0.51286±3), ²³⁰Th/²³²Th (0.65±0.02), Th/U (4.08±0.07) ratios, and to a lesser extent ¹⁸O values (+5.8 to +6.4 % SMOW) and ⁸⁷Sr/⁸⁶Sr ratios (0.70440 to 0.70468) is compatible with a magmatic evolution through fractional crystallization without significant crustal contamination. Nevertheless low-¹⁸O and high ⁸⁷Sr/⁸⁶Sr values in basaltic andesites may be due to the introduction of meteoric fluids into the Galunggung magma.     

Crystallization history of Kilauea Iki lava lake as seen in drill core recovered in 1967–1979

Kilauea Iki lava lake formed during the 1959 summit eruption, one of the most picritic eruptions of Kilauea Volcano in the twentieth century. Since 1959 the 110 to 122 m thick lake has cooled slowly, developing steadily thickening upper and lower crusts, with a lens of more molten lava in between. Recent coring dates, with maximum depths reached in the center of the lake, are: 1967 (26.5 m). 1975 (44.2 m), 1976 (46.0 m) and 1979 (52.7 m). These depths define the base of the upper crust at the time of drilling. The bulk of the core consists of a gray, olivine-phyric basalt matrix, which locally contains coarser-grained diabasic segregation veins. The most important megascopic variation in the matrix rock is its variation in olivine content. The upper 15 m of crust is very olivine-rich. Abundance and average size of olivine decrease irregularly downward to 23 m; between 23 and 40 m the rock contains 5–10% of small olivine phenocrysts. Below 40 m. olivine content and average grainsize rise sharply. Olivine contents remain high (20–45%, by volume) throughout the lower crust, except for a narrow (< 6 m) olivine depleted zone near the basalt contact. Petrographically the olivine phenocrysts in Kilauea Iki can be divided into two types. Type 1 phenocrysts are large (1–12 mm long), with irregular blocky outlines, and often contain kink bands. Type 2 crystals are relatively small (0.5–2 mm in length), euhedral and undeformed. The variations in olivine content of the matrix rock are almost entirely variations in the amount of type 1 olivines. Sharp mineral layering of any sort is rare in Kilauea Iki. However, the depth range 41–52 m is marked by the frequent occurrence of steeply dipping (70°–90°) bands or bodies of slightly vuggy olivine-rich rock locally capped with a small cupola of segregation-vein material. In thin section there is clear evidence for relative movement of melt and crystals within these structures. The segregation veins occur only in the upper crust. The most widely distributed (occurring from 4.5–59.4 m) are thin veins (most < 5 cm thick), which cut the core at moderate angles and appear to have been derived from the immediately adjacent wall-rock by filter pressing. There is also a series of thicker (0.1–1.5 m) segregation veins, which recur every 2–3 m, between 20 and 52 m. These have subhorizontal contacts and appear, from similarities in thickness and spacing, to correlate between drill holes as much as 100 m apart. These large veins are not derived from the adjacent wallrock: their mechanism of formation is still problematical. The total thickness of segregation veins in Kilauea Iki is 3–6 m in the central part of the lake, corresponding to 6–11% of the upper crust. Whole-rock compositions for Kilauea Iki fall into two groups: the matrix rock ranges from 20-7.5% MgO, while the segregation veins all contain between 6.0 and 4.5% MgO. There are no whole-rock compositions of intermediate MgO content. Samples from < 12 m show eruption-controlled chemistry. Below that depth, matrix rock compositions have higher Al₂O₃, TiO₂ and alkalies, and lower CaO and FeO, at a given MgO content than do the eruption pumices. The probable causes of this are assimilation of low-melting components from foundered crust, plus removal of olivine, plus removal of minor augite, for rocks with MgO contents of < 8.0%. Given the observed rate of growth of the upper crust, one can infer that significant removal of the type 1 olivine phenocrysts from the upper part of the lake began in 1963 and ceased sometime prior to 1972. The process. probably gravitative settling, appears to have been inhibited earlier by gas streaming from the lower part of the lens of melt. The olivine cumulate zone, which extends into the upper crust, contains relatively few (25–40%) olivine crystals, few of which actually touch each other. The diffuseness of the cumulate zone raises the possibility that the crystals were coated with a relatively visous boundary layer of melt which moved with them. Calculations of the Stokes’ law settling rates of the largest olivine crystals found at the base of the crust in 1975–76 suggest that the «melt» had a viscosity of > 10⁶ poises, and probably had the properties of a Bingham body, rather than a Newtonian fluid, by that date, which was several years after olivine removal ceased.     

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.     

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.     

Chromite in the Paricutin lava flows (1943–1952)

Small euhedral chromite crystals are found in olivine macrophenocrysts (Fo_80–84) from the basaltic andesites (150 ppm Cr) erupted in 1943–1947, and in orthopyroxene macrophenocrysts of the andesites (75 ppm Cr) erupted in 1947–1952. The majority of the chromite octahedra are 5–20 μm in diameter, and some are found in clusters and linear chains of three or more oriented chromite crystals. The composition of the majority of the chromite grains within olivine and orthopyroxene macrophenocrysts is Fe²⁺/(Fe²⁺+Mg)=0.5–0.6, Cr/(Cr+Al)=0.5–0.6 and Fe³⁺/(Fe³⁺+Al+Cr)=0.2–0.3. The chromite crystals in contact with the groundmass are larger, subhedral, and grade in composition from chromite cores to magnetite rims. Comparison of the composition of chromite with those of other volcanic rocks shows that the most primitive Paricutin chromite is richer in total iron and higher in Fe³⁺/(Fe³⁺+Al+Cr) than primary chromite in most lavas. The linear chains of oriented chromite octahedra are found in olivine and orthopyroxene macrophenocrysts, and in the groundmass. These chromite chains are thought to result from diffusion-controlled crystallization because of the very high partition coefficient (1000) of Cr between chromite and melt. We conclude that chromite was a primary phase in the lavas at the time of extrusion and that magnetite only crystallized after extrusion during cooling of the lava flows. The presence of chromite microphenocrysts in andesitic lavas containing as little as 70 ppm Cr can be explained by dissolved H₂O in the melt depressing the liquidus temperature for orthopyroxene such that chromite becomes a liquidus phase. The influence of dissolved H₂O can also explain the lack of plagioclase macrophenocrysts in most of the lavas and the relatively high partition coefficient (20) of Ni between olivine and melt and the high partition coefficient (40) of Cr between orthopyroxene and melt. The liquidus temperature of the basaltic andesite is estimated to have been less than 1140°C, assuming H₂O>1 wt.%, and the log f_O2 to have been above that of the QFM buffer. The chromite and orthopyroxene liquidus temperature of the andesites, assuming H₂O>1 wt.%, is estimated to have been 1100°C or less. The derivation of the later andesites from the earlier basaltic andesites has been explained by a combination of fractional crystallization of olivine, orthopyroxene and plagioclase, and assimilation of xenoliths. The significantly lower Cr, Ni and Mg of the andesites may have been in part due to the separation of olivine macrophenocrysts plus enclosed chromite crystals from the earlier basaltic andesites.     

Ultrasonic measurements of Vp and Qp: relaxation spectrum of complex modulus on basalt melts

Ultrasonic compressional wave velocity V_p and quality factor Q_p have been measured in alkali basalt, olivine basalt and basic andesite melts in the frequency range of 3.4–22 MHz and in the temperature range of 1100–1400°C. Velocity and attenuation of the melts depend on frequency and temperature, showing that there are relaxation mechanisms in the melts. Complex moduli are calculated from the ultrasonic data. The results fit well a complex modulus of Arrhenius temperature dependence with log-normal Gaussian distribution in relaxation times of attenuation. The analysis yields average relaxation time, its activation energy, relaxed modulus, unrelaxed modulus and width of Gaussian distribution in relaxation times. Relaxed modulus is smaller (17.5 GPa) for basic andesite melt of high silica and high alumina contents than for the other two basalt melts (18.1–18.4 GPa). The most probable relaxation times decrease from ～ 3 × 10^?10 s for basic andesite to ～ 10^?11 s for alkali basalt at 1400°C. Activation energies of attenuation, ranging from 270 to 340 kJ mol^?1 in the three melts, are highest in basic andesite. Longitudinal viscosity values and their temperature dependences are also calculated from V_p and Q_p data. The volume viscosity values are estimated from the data using the shear viscosity values. Longitudinal, volume and shear viscosities and their activation energies are highest in the basic andesite melt of the most polymerized structure.     

Origin of high-magnesian andesites in the Setouchi volcanic belt,southwest Japan,II. Melting phase relations at high pressures

Melting phase relations of an augite-olivine high-magnesian andesite and an augite-olivine basalt from the Miocene Setouchi volcanic belt in southwest Japan have been studied under water-saturated, water-undersaturated and under anhydrous conditions. Both the andesite and the basalt are characterized by low FeO*/MgO ratios (0.86 and 0.76 in weight, respectively) and qualify as primary magmas derived from the upper mantle.The andesite melt coexists with olivine, orthopyroxene and clinopyroxene at 15 kbar and 1030°C under water-saturated conditions, and at 10 kbar and 1070°C under water-undersaturated conditions (7 wt.% H₂O in the melt). The basalt-melt also coexists with the above three phases at 11 kbar and 1305°C under anhydrous conditions, and at 15 kbar and 1205°C in the presence of 4 wt.% water.Present studies indicate that high-magnesian andesite magmas may be produced even under water-undersaturated conditions by partial melting of mantle peridotite. It is suggested that two types of high-magnesian andesites in the Setouchi volcanic belt (augite-olivine and bronzite-olivine andesites) were produced by different degrees of partial melting; augite-olivine andesite magmas, whose mantle residual is lherzolite, were formed by lower degrees of partial melting than bronzite-olivine andesite magmas, which coexist with harzburgite. The basalt magmas, which were often extruded in close proximity to the high-magnesian andesite magmas, are not partial melting products of a mantle peridotite which had previously melted to yield high-magnesian andesite magmas.     

Lateral variations of H2O contents in quaternary magmas of Northeastern Japan

Volcanoes of the East Japan volcanic arc are divided into two groups on the basis of their phenocryst assemblages; volcanoes with lavas or pyroclastic rocks containing quartz phenocrysts and no hornblende phenocrysts (type A), and those with rocks containing hornblende phenocrysts and no quartz phenocrysts (type B). Type A volcanoes occur only in the narrow region along the volcanic front, whereas type B volcanoes are distributed in the area closer to the Sea of Japan.Recent experimental studies on calc-alkaline andesite-dacite under H₂O-saturated and -undersaturated conditions indicate that the liquidus temperature (maximum thermal stability limit) of quartz decreases drastically with increasing H₂O content in magma, whereas the liquidus temperatures of hornblende and biotite are relatively constant with variations in the H₂O content and bulk chemical composition of the magma.It is suggested from the lateral variation of mafic phenocryst assemblages [1] and from the above result that the temperature of the parental magmas of these volcanoes increases, and their H₂O contents decrease, towards the volcanic front in the East Japan volcanic arc.Such lateral variations in the H₂O contents of magmas under the East Japan volcanic arc are in agreement with those of other incompatible elements (K, Rb, REE, etc.). If H₂O-undersaturated partial melting of upper mantle peridotite can be represented by the univariant line (olivine, Ca-rich clinopyroxene, orthopyroxene and liquid coexist) in the system H₂OMg₂SiO₄z.sbnd;CaMgSi₂O₆z.sbnd;SiO₂, the decrease of H₂O content in the magma suggests that the melting temperature of the peridotitic mantle may gradually increase, and so the degree of partial melting may increase, towards the volcanic front. The lateral variation of other incompatible elements can also be explained by this model.     

Scapolite phenocrysts in a latite dome,northwest Arizona,U.S.A.

A latite dome in northwest Arizona contains a rare occurrence of primary SO₄-rich scapolite phenocrysts. The total phenocryst assemblage consists of plagioclase (An₂₀?An₃₃), hornblende, biotite, and scapolite (Me₆₈). Microphenocrysts include allanite and oxidized low-Ti magnetite. Electron microprobe analyses show that the scapolite contains about 1.74 wt.% S, which indicates an atomic S/(S + C) of 0.58. Although scapolite occurs in xenoliths in volcanic rocks and diatremes, as well as a metamorphic mineral in granulites, its occurrence as a primary igneous mineral is extremely rare.Ca-rich scapolite has been crystallized experimentally by others from melts with a wide range of SiO₂, CaO, and Na₂O contents, at temperatures above 825°C and pressures ranging from 3 to 15 kbar. Comparison of scapolite from this latite with synthetic scapolite crystallized from nepheline syenite melt suggests that the Arizona phenocrysts crystallized under conditions of 850 to 900°C, 3–6 kbar total pressure, and unusually high ?_CO2 and ?_SO2. The rarity of scapolite as a phenocryst mineral suggests that high partial pressures of CO₂ and SO₂ are rare in the magmatic environment.     

Geobarometry of ultramafic xenoliths from Loihi Seamount,Hawaii, on the basis of CO2 inclusions in olivine

Abundant fluid inclusions in olivine of dunite xenoliths (～1–3 cm) in basalt dredged from the young Loihi Seamount, 30 km southeast of Hawaii, are evidence for three coexisting immiscible fluid phases—silicate melt (now glass), sulfide melt (now solid), and dense supercritical CO₂ (now liquid + gas)—during growth and later fracturing of some of these olivine crystals. Some olivine xenocrysts, probably from disaggregation of xenoliths, contain similar inclusions.Most of the inclusions (2–10 μm) are on secondary planes, trapped during healing of fractures after the original crystal growth. Some such planes end abruptly within single crystals and are termed pseudosecondary, because they formed during the growth of the host olivine crystals. The “vapor” bubble in a few large (20–60 μm), isolated, and hence primary, silicate melt inclusions is too large to be the result of simple differential shrinkage. Under correct viewing conditions, these bubbles are seen to consist of CO₂ liquid and gas, with an aggregate ? = ～ 0.5–0.75 g cm^?3, and represent trapped globules of dense supercritical CO₂ (i.e., incipient “vesiculation” at depth). Some spinel crystals enclosed within olivine have attached CO₂ blebs. Spherical sulfide blebs having widely variable volume ratios to CO₂ and silicate glass are found in both primary and pseudosecondary inclusions, demonstrating that an immiscible sulfide melt was also present.Assuming olivine growth at ～ 1200°C and hydrostatic pressure from a liquid lava column, extrapolation of CO₂P-V-T data indicates that the primary inclusions were trapped at ～ 220–470 MPa (2200–4700 bars), or ～ 8–17 km depth in basalt magma of ? = 2.7 g cm^?3. Because the temperature cannot change much during the rise to eruption, the range of CO₂ densities reveals the change in pressure from that during original olivine growth to later deformation and rise to eruption on the sea floor. The presence of numerous decrepitated inclusions indicates that the inclusion sample studied is biased by the loss of higher-density inclusions and suggests that some part of these olivine xenoliths formed at greater depths.     

The lesser antilles — A discussion of the Island arc magmatism

The active island arc of Lesser Antilles marks the junction between the Atlantic and Carribbean lithospheric plates. With the exception of the alkali basalts of Grenada, the volcanics of the arc can be regarded as belonging to the low-K, island arc, calc-alkaline suite. Although compositions ranging from basalt to rhyolite have been described, porphyritic andesite appears to be the dominant rock type on most volcanoes (intermediate centers). Variable amounts of basalt and basaltic andesite occur and rarely predominate over andesite (latter are basic centers), whereas the more silicic members are only occasionally found. The calc-alkaline suite is characterized by relatively high Al₂O₃ and CaO and low K₂O, Rb and Ni. Variations, especially in the alkali elements, occur both with space and time. A characteristic feature of many of the volcanoes is the occurrence in the basalt and basaltic andesite volcanics of plutonic blocks, often showing cumulate textures. The blocks which ware composed of plagioclase — amphibole — olivine — clinopyroxene — magnetite are thought to be the products of fractionation. The differences between basic and intermediate centers is probably due to the frequency that the magma ascended to the surface or remained in high level chambers where fractionation occurred.     

Volcanic rocks of the Witu Islands,Papua New Guinea: The origin of magmas above the deepest part of the New Britain Benioff zone

The Witu Islands are Quaternary volcanoes that overlie the deepest (about 300–580 km) part of the New Britain Benioff zone. The islands are about 100 km south of the transcurrent-divergent plate boundary that crosses the Bismarck Sea, and they surmount the southeastern end of the Willaumez-Manus Rise. The rocks are olivine- and quartz-normative tholeiitic basalts, low- and high-SiO₂ andesites, dacites, and rhyolites. Alkaline rocks that overlie the deep (greater than 300 km) parts of other Benioff zones have not been found in the Witu Islands. Compared to the Witu Islands rocks, those with similar SiO₂ contents from New Britain volcanoes that overlie progressively shallower parts of the Benioff zone to the south, are, for example, generally poorer in Na+K, Ti, and P, and higher in Ca and Al. There are similar progressive changes in trace-element abundances, but Zr and Nb contents are distinctly richer in Witu Islands rocks.⁸⁷Sr/⁸⁶Sr values range between 0.70311 and 0.7038, which are typical for rocks from New Britain as a whole and from other island arcs in the southwest Pacific. Two¹⁴³Nd/¹⁴⁴Nd values of 0.512211 and 0.512271, taken together with the Sr isotopic results, define a source region equivalent to those for oceanic-island basalts; there is no evidence for sea-water contamination of the sources. Perhaps the most striking feature of the Witu Islands rocks is their compositional diversity. Basalts range from olivine tholeiites similar to marginal-basin basalts from other areas, to quartz tholeiites similar in most respects to those typical of island arcs, and to incompatible-element-enriched tholeiites that are close to silica-undersaturation. Andesites on Unea Island have a strong island-arc signature, but the andesites, dacites, and rhyolite of Garove Island have some features that may be more in common with the silica-oversaturated rocks of oceanic areas. The mineralogy of Witu Islands basalts is characterised by phenocrysts of olivine (Fo_89-54), plagioclase (An_90-55) and Ca-augite. Cr-Al-rich spinels and aluminous magnetites are present as inclusions in some olivine phenocrysts. Groundmass fayalite, alkali feldspar, and dacitic to rhyolitic glasses high in K/Na are found in a few samples. In contrast to basalts from volcanoes above the shallower parts of the New Britain Benioff zone, those of the Witu Islands are characterised by rarity of low-Ca pyroxene, as phenocrysts or in the groundmass. Rocks richer in SiO₂ are characterised by the presence of orthopyroxene phenocrysts and lesser amounts of olivine. Hydrous minerals appear to be absent. Groundmass Fe-Ti oxides define crystallisation temperatures (about 800–1050°C) and oxygen fugacities (fO₂) corresponding to those of the Ni-NiO buffer, but up to two fO₂ log units above it. The suite as a whole is phenocryst-poor compared to most New Britain volcanic rocks. A significant degree of mantle heterogeneity is inferred by the chemical variability of the Witu Islands rocks. However, there are no compelling reasons in support of the interpretation that source heterogeneity is due to the effect of a slab-derived component. The cause of the heterogeneity is unclear, but may be due to mantle differentiation processes related to an anomalous tectonic setting.     

The November 2002 eruption of Piton de la Fournaise,Réunion: tracking the pre-eruptive thermal evolution of magma using melt inclusions

The November 2002 eruption of Piton de la Fournaise in the Indian Ocean was typical of the activity of the volcano from 1999 to 2006 in terms of duration and volume of magma ejected. The first magma erupted was a basaltic liquid with a small proportion of olivine phenocrysts (Fo₈₁) that contain small numbers of melt inclusions. In subsequent flows, olivine crystals were more abundant and richer in Mg (Fo_83–84). These crystals contain numerous melt and fluid inclusions, healed fractures, and dislocation features such as kink bands. The major element composition of melt inclusions in this later olivine (Fo_83–84) is out of equilibrium with that of its host as a result of extensive post-entrapment crystallization and Fe²⁺ loss by diffusion during cooling. Melt inclusions in Fo₈₁ olivine are also chemically out of equilibrium with their hosts but to a lesser degree. Using olivine–melt geothermometry, we determined that melt inclusions in Fo₈₁ olivine were trapped at lower temperature (1,182 ± 1°C) than inclusions in Fo_83–84 olivine (1,199–1,227°C). This methodology was also used to estimate eruption temperatures. The November 2002 melt inclusion compositions suggest that they were at temperatures between 1,070°C and 1,133°C immediately before eruption and quenching. This relatively wide temperature range may reflect the fact that most of the melt inclusions were from olivine in lava samples and therefore likely underwent minor but variable amounts of post-eruptive crystallization and Fe²⁺ loss by diffusion due to their relatively slow cooling on the surface. In contrast, melt inclusions in tephra samples from past major eruptions yielded a narrower range of higher eruption temperatures (1,163–1,181°C). The melt inclusion data presented here and in earlier publications are consistent with a model of magma recharge from depth during major eruptions, followed by storage, cooling, and crystallization at shallow levels prior to expulsion during events similar in magnitude to the relatively small November 2002 eruption.     

The Natash alkaline volcanic field,Egypt: geochemical and mineralogical inferences on the evolution of a basalt to rhyolite eruptive suite

Extensive lava flows were erupted during the Upper Cretaceous in the Wadi Natash of southern Egypt. The lavas are mainly of alkaline (sodium dominated) composition and include alkali olivine basalt (AOB), hawaiite, mugearite, and benmoreite that intruded with acidic volcanics of trachytic to rhyolitic composition. Abundances of major oxides and trace elements including the REE vary systematically through this compositional spectrum. The gradual decrease of CaO with decreasing MgO is consistent with the dominance of phenocrysts of labradoritic plagioclase (An_75–62) and Mg-rich olivine (Fo_84–80) in the AOB and hawaiite. Olivine phenocrysts are normally zoned with cores consistent with crystallization from a magma having the bulk-rock composition. The sharp decrease of alkalis at low MgO contents (∼0.4% MgO) indicates significant alkali feldspar fractionation during the evolution of trachytes and rhyolites. All Natash lavas show steep chondrite-normalized REE patterns with considerable LREE/HREE fractionation and a regular decrease in La/Lu ratios from the least to the most evolved lavas (La/Lu_n=12.5−9.5). The low absolute abundances of HREE in basic members reflects residual garnet in the source. The basic lavas have experienced compositional modifications after they segregated from the source as evidenced by lower averages of Mg^# (51), Ni (134) and Cr (229) in the AOB. Much of this variation can be explained by variable degrees of polybaric fractional crystallization. Petrographic and geochemical data supported by quantitative modelling suggest the evolution of the Natash Lavas from a common AOB parent in multiple, short-lived magma chambers. In agreement with the phenocryst mineralogy of the Natash lavas, the geochemical models suggest that with increasing degree of differentiation, Mg-rich olivine, calcic plagioclase, and augite are joined and progressively substituted by ferrohedenbergite, alkali feldspars and magnetite. The OIB (ocean island basalt)-like nature of the AOB and hawaiite lavas suggests that the volumetrically dominant source component is the asthenospheric mantle. A mantle-plume source is suggested for the Natash basaltic lavas, with the lavas being generated by partial melting of a garnet peridotite in the asthenosphere.     

Petrogenesis of basalts from the project FAMOUS area: experimental study from 0 to 15 kbars

Tholeiitic basalt glasses from the FAMOUS area of the Mid-Atlantic Ridge are among the most primitive basaltic liquids reported from the ocean basins. One of the more primitive of these[Mg/(Mg+Fe²⁺) = 0.68;Ni= 232ppm;TiO₂ = 0.61] glasses (572-1-1) was selected for an experimental investigation. This study found olivine to be the liquidus phase from 1 atm to 10.5 kbar where it is replaced by clinopyroxene. The sequence of appearance of phases at 1 atm pressure is olivine (1268°C), plagioclase (1235°C) and clinopyroxene (1135°C). The sample is multiply saturated at 10.5 kbar with olivine (Fo₈₈), clinopyroxene (Wo₃₂En₆₀Fs₉), and orthopyroxene (Wo₅En₈₃Fs₁₂). From the 1-atm data we have measured (FeO/MgO) olivine/(FeO*/MgO) liquid (K′_D) for olivine-melt pairs equilibrated at 12 temperatures in the range 1268–1205°C.K′_D varies from 0.30 at 1205°C to 0.27 at 1268°C. Analysis of high-pressure olivine melt pairs indicates a systematic increase inK′_D with pressure.Evaluation of the 1-atm experiments reveals that fractionation of olivine followed by olivine + plagioclase can generate much of the variation in major element chemistry observed in the FAMOUS basalt glasses. However, it cannot account for the entire spectrum of glass compositions — particularly with respect to TiO₂ and Na₂O. The variations in these components are such as to require different primary liquids.Comparison of clinopyroxene microphenocrysts/xenocrysts found in oceanic tholeiites with experimental clinopyroxenes reveal that the majority of those in the tholeiites may have crystallized from the magma at pressures greater than ～ 10 kbar and are not accidental xenocrysts. Clinopyroxene fractionation at high pressures may be a viable mechanism for fractionating basaltic magmas.The major and minor element mineral/meltK′_d's from our experiments have been used to model the source region residual mineralogy for given percentages of partial melting. These data suggest that ～20% partial melting of a lherzolite source containing 0–10% clinopyroxene can generate the major and minor element concentrations in the parental magmas of the Project FAMOUS basalt glasses.