Revisiting the compositions and volatile contents of olivine-hosted melt inclusions from the Mount Shasta region: implications for the formation of high-Mg andesites

Primitive chemical characteristics of high-Mg andesites (HMA) suggest equilibration with mantle wedge peridotite, and they may form through either shallow, wet partial melting of the mantle or re-equilibration of slab melts migrating through the wedge. We have re-examined a well-studied example of HMA from near Mt. Shasta, CA, because petrographic evidence for magma mixing has stimulated a recent debate over whether HMA magmas have a mantle origin. We examined naturally quenched, glassy, olivine-hosted (Fo_87–94) melt inclusions from this locality and analyzed the samples by FTIR, LA-ICPMS, and electron probe. Compositions (uncorrected for post-entrapment modification) are highly variable and can be divided into high-CaO (>10 wt%) melts only found in Fo > 91 olivines and low-CaO (<10 wt%) melts in Fo 87–94 olivine hosts. There is evidence for extensive post-entrapment modification in many inclusions. High-CaO inclusions experienced 1.4–3.5 wt% FeO^T loss through diffusive re-equilibration with the host olivine and 13–28 wt% post-entrapment olivine crystallization. Low-CaO inclusions experienced 1–16 wt% olivine crystallization with <2 wt% FeO^T loss experienced by inclusions in Fo > 90 olivines. Restored low-CaO melt inclusions are HMAs (57–61 wt% SiO₂; 4.9–10.9 wt% MgO), whereas high-CaO inclusions are primitive basaltic andesites (PBA) (51–56 wt% SiO₂; 9.8–15.1 wt% MgO). HMA and PBA inclusions have distinct trace element characteristics. Importantly, both types of inclusions are volatile-rich, with maximum values in HMA and PBA melt inclusions of 3.5 and 5.6 wt% H₂O, 830 and 2,900 ppm S, 1,590 and 2,580 ppm Cl, and 500 and 820 ppm CO₂, respectively. PBA melts are comparable to experimental hydrous melts in equilibrium with harzburgite. Two-component mixing between PBA and dacitic magma (59:41) is able to produce a primitive HMA composition, but the predicted mixture shows some small but significant major and trace element discrepancies from published whole-rock analyses from the Shasta locality. An alternative model that involves incorporation of xenocrysts (high-Mg olivine from PBA and pyroxenes from dacite) into a primary (mantle-derived) HMA magma can explain the phenocryst and melt inclusion compositions but is difficult to evaluate quantitatively because of the complex crystal populations. Our results suggest that a spectrum of mantle-derived melts, including both PBA and HMA, may be produced beneath the Shasta region. Compositional similarities between Shasta parental melts and boninites imply similar magma generation processes related to the presence of refractory harzburgite in the shallow mantle.     

High-Mg# andesitic lavas of the Shisheisky Complex,Northern Kamchatka: implications for primitive calc-alkaline magmatism

Primitive arc magmatism and mantle wedge processes are investigated through a petrologic and geochemical study of high-Mg# (Mg/Mg + Fe > 0.65) basalts, basaltic andesites and andesites from the Kurile-Kamchatka subduction system. Primitive andesitic samples are from the Shisheisky Complex, a field of Quaternary-age, monogenetic cones located in the Aleutian–Kamchatka junction, north of Shiveluch Volcano, the northernmost active composite volcano in Kamchatka. The Shisheisky lavas have Mg# of 0.66–0.73 at intermediate SiO₂ (54–58 wt%) with low CaO (<8.8%), CaO/Al₂O₃ (<0.54), and relatively high Na₂O (>3.0 wt%) and K₂O (>1.0 wt%). Olivine phenocryst core compositions of Fo90 appear to be in equilibrium with whole-rock ‘melts’, consistent with the sparsely phyric nature of the lavas. Compared to the Shisheisky andesites, primitive basalts from the region (Kuriles, Tolbachik, Kharchinsky) have higher CaO (>9.9 wt%) and CaO/Al₂O₃ (>0.60), and lower whole-rock Na₂O (<2.7 wt%) and K₂O (<1.1 wt%) at similar Mg# (0.66–0.70). Olivine phenocrysts in basalts have in general, higher CaO and Mn/Fe and lower Ni and Ni/Mg at Fo88 compared to the andesites. The absence of plagioclase phenocrysts from the primitive andesitic lavas contrasts the plagioclase-phyric basalts, indicating relatively high pre-eruptive water contents for the primitive andesitic magmas compared to basalts. Estimated temperature and water contents for primitive basaltic andesites and andesites are 984–1,143°C and 4–7 wt% H₂O. For primitive basalts they are 1,149–1,227°C and 2 wt% H₂O. Petrographic and mineral compositions suggest that the primitive andesitic lavas were liquids in equilibrium with mantle peridotite and were not produced by mixing between basalts and felsic crustal melts, contamination by xenocrystic olivine, or crystal fractionation of basalt. Key geochemical features of the Shisheisky primitive lavas (high Ni/MgO, Na₂O, Ni/Yb and Mg# at intermediate SiO₂) combined with the location of the volcanic field above the edge of the subducting Pacific Plate support a genetic model that involves melting of eclogite or pyroxenite at or near the surface of the subducting plate, followed by interaction of that melt with hotter peridotite in the over-lying mantle wedge. The strongly calc-alkaline igneous series at Shiveluch Volcano is interpreted to result from the emplacement and evolution of primitive andesitic magmas similar to those that are present in nearby monogenetic cones of the Shisheisky Complex.     

Evolution of parental magmas of Miocene shield basalts of Gran Canaria (Canary Islands): constraints from crystal,melt and fluid inclusions in minerals

 Picritic units of the Miocene shield volcanics on Gran Canaria, Canary Islands, contain olivine and clinopyroxene phenocrysts with abundant primary melt, crystal and fluid inclusions. Composition and crystallization conditions of primary magmas in equilibrium with olivine Fo_90-92 were inferred from high-temperature microthermometric quench experiments, low-temperature microthermometry of fluid inclusions and simulation of the reverse path of olivine fractional crystallization based on major element composition of melt inclusions. Primary magmas parental for the Miocene shield basalts range from transitional to alkaline picrites (14.7–19.3 wt% MgO, 43.2–45.7 wt% SiO₂). Crystallization of these primary magmas is believed to have occurred over the temperature range 1490–1150° C at pressures ≈5 kbar producing olivine of Fo_80.6-90.2, high-Ti chrome spinel [Mg/ (Mg+Fe²⁺)=0.32–0.56, Cr/(Cr+Al)=0.50–0.78, 2.52–8.58 wt% TiO₂], and clinopyroxene [Mg/(Mg+Fe)=0.79–0.88, Wo_44.1-45.3, En_43.9-48.0, Fs_6.8-11.0] which appeared on the liquidus together with olivine≈Fo₈₆. Redox conditions evolved from intermediate between the QFM and WM buffers to late-stage conditions of NNO+1 to NNO+2. The primary magmas crystallized in the presence of an essentially pure CO₂ fluid. The primary magmas originated at pressures >30 kbar and temperatures of 1500–1600° C, assuming equilibrium with mantle peridotite. This implies melting of the mantle source at a depth of ≈100 km within the garnet stability field followed by migration of melts into magma reservoirs located at the boundary between the upper mantle and lower crust. The temperatures and pressures of primary magma generation suggest that the Canarian plume originated in the lower mantle at depth ≈900 km that supports the plume concept of origin of the Canary Islands. Received: 23 October 1995/Accepted: 21 February 1996     

Plagioclase-free andesites from Zitácuaro (Michoacán), Mexico: petrology and experimental constraints

Approximately 150 km west of Mexico City in the central part of the Mexican Volcanic Belt (MVB) near Zitácuaro, Mexico, young volcanism has produced shield volcanoes, large volume silicic deposits, and fault-related basalt and andesite lava flows and cinder cones. This paper concerns a small cluster of Pleistocene andesite cones and flows which can be separated into two distinct groups: high-magnesium andesites (>6% MgO, 57–59% SiO₂), conveniently called basaltic andesites, with phenocrysts of orthopyroxene and augite, or augite and olivine; and andesites (60–62% SiO₂, <4.6% MgO), which have phenocrysts of orthopyroxene and augite, and ghosts of relict hornblende. Remarkably, plagioclase phenocrysts are absent, and evenly distributed but sparse (0.5–3.5%) quartz xenocrysts are present in all the lavas. In order to establish the conditions under which early crystallizing plagioclase is suppressed in these lavas, water saturated experiments up to 3 kbars were performed on one of the basaltic andesites. The conditions required to reproduce the phenocryst assemblages (either olivine + augite or opx + augite) are temperatures in excess of 1000 °C, with water saturated liquids (>3 wt%) at pressures of about 1 kbar. Compared to basaltic andesites of western Mexico, the Zitácuaro basaltic andesites have ∼2 wt% lower Al₂O₃ concentrations, which causes plagioclase to precipitate at significantly lower temperatures, and it therefore follows the crystallization sequence: olivine, augite, and orthopyroxene. Based on ubiquitous quartz xenocrysts, with glassy rhyolitic inclusions, a reasonable conclusion is that substantial mixing of a quartz-bearing rhyolitic magma with a parental basaltic andesite has occurred at low pressure (shallow depth), and this would account for the low Al₂O₃ concentrations in the Zitácuaro basaltic andesites. Whatever the mechanism of incorporation, the quartz xenocrysts are evidence of contamination of basaltic magma with more siliceous material, thus making it difficult to use these magmas as indicators of mantle melting processes. Received: 29 July 1997 / Accepted: 29 January 1998     

The origin of high-Mg magmas in Mt Shasta and Medicine Lake volcanoes,Cascade Arc (California): higher and lower than mantle oxygen isotope signatures attributed to current and past subduction

We report the oxygen isotope composition of olivine and orthopyroxene phenocrysts in lavas from the main magma types at Mt Shasta and Medicine Lake Volcanoes: primitive high-alumina olivine tholeiite (HAOT), basaltic andesites (BA), primitive magnesian andesites (PMA), and dacites. The most primitive HAOT (MgO > 9 wt%) from Mt. Shasta has olivine δ¹⁸O (δ¹⁸O_Ol) values of 5.9–6.1‰, which are about 1‰ higher than those observed in olivine from normal mantle-derived magmas. In contrast, HAOT lavas from Medicine Lake have δ¹⁸O_Ol values ranging from 4.7 to 5.5‰, which are similar to or lower than values for olivine in equilibrium with mantle-derived magmas. Other magma types from both volcanoes show intermediate δ¹⁸O_Ol values. The oxygen isotope composition of the most magnesian lavas cannot be explained by crustal contamination and the trace element composition of olivine phenocrysts precludes a pyroxenitic mantle source. Therefore, the high and variable δ¹⁸O_Ol signature of the most magnesian samples studied (HAOT and BA) comes from the peridotitic mantle wedge itself. As HAOT magma is generated by anhydrous adiabatic partial melting of the shallow mantle, its 1.4‰ range in δ¹⁸O_Ol reflects a heterogeneous composition of the shallow mantle source that has been influenced by subduction fluids and/or melts sometime in the past. Magmas generated in the mantle wedge by flux melting due to modern subduction fluids, as exemplified by BA and probably PMA, display more homogeneous composition with only 0.5‰ variation. The high-δ¹⁸O values observed in magnesian lavas, and principally in the HAOT, are difficult to explain by a single-stage flux-melting process in the mantle wedge above the modern subduction zone and require a mantle source enriched in ¹⁸O. It is here explained by flow of older, pre-enriched portions of the mantle through the slab window beneath the South Cascades.     

Coexistence of two distinct mantle sources during formation of ophiolites: a case study of primitive pillow-lavas from the lowest part of the volcanic section of the Troodos Ophiolite, Cyprus

We present a detailed mineralogical, petrological and melt inclusion study of unusually fresh, primitive olivine + clinopyroxene phyric Lower Pillow Lavas (LPL) found near Analiondas village in the northeastern part of the Troodos ophiolite (Cyprus). Olivine phenocrysts in these primitive LPL show a wide compositional range (Fo_82–92) and have higher CaO contents than those from the Upper Pillow Lavas (UPL). Cr-spinel inclusions in olivine are significantly less Cr-rich (Cr/Cr + Al = 28–67 mol%) compared to those from the UPL (Cr# = 70–80). These features reflect differences in melt compositions between primitive LPL and the UPL, namely higher CaO and Al₂O₃ and lower FeO* compared to the UPL at a given MgO. LPL parental melts (in equilibrium with Fo₉₂) had ∼10.5 wt% MgO and crystallization temperatures ∼1210 °C, which are significantly lower than those previously published for the UPL (14–15 wt% MgO and ∼1300 °C for Fo₉₂). The fractionation path of LPL parental melts is also different from that of the UPL. It is characterized initially by olivine + clinopyroxene cotectic crystallization joined by plagioclase at ∼9 wt% MgO, whereas UPL parental melts experienced a substantial interval of olivine-only crystallization. Primitive LPL melts were formed from a mantle source which was more fertile than that of tholeiites from well-developed intra-oceanic arcs, but broadly similar in its fertility to that of Mid-Ocean Ridge Basalt (MORB) and Back Arc Basin Basalts (BABB). The higher degrees of melting during formation of the LPL primary melts compared to average MORB were caused by the presence of subduction-related components (H₂O). Our new data on the LPL coupled with existing data for the UPL support the existing idea that the LPL and UPL primary melts originated from distinct mantle sources, which cannot be related by progressive source depletion. Temperature differences between these sources (∼150 °C), their position in the mantle (∼10 kbar for the colder LPL source vs 15–18 kbar for the UPL source), and temporal succession of Troodos volcanism, all cannot be reconciled in the framework of existing models of mantle wedge processes, thermal structure and evolution, if a single mantle source is invoked. Possible tectonic settings for the origin of the Troodos ophiolite (forearc regions of intra-oceanic island arc, propagation of backarc spreading into arc lithosphere) are discussed. Received: 20 May 1996 / Accepted: 25 March 1997     

Quaternary volcanism near the Valley of Mexico: implications for subduction zone magmatism and the effects of crustal thickness variations on primitive magma compositions

The Valley of Mexico and surrounding regions of Mexico and Morelos states in central Mexico contain more than 250 Quaternary eruptive vents in addition to the large, composite volcanoes of Popocatépetl, Iztaccíhuatl, and Nevado de Toluca. The eruptive vents include cinder and lava cones, shield volcanoes, and isolated andesitic and dacitic lava flows, and are most numerous in the Sierra Chichináutzin that forms the southern terminus of the Valley of Mexico. The Chichináutzin volcanic field (CVF) is part of the E-W-trending Mexican Volcanic Belt (MVB), a subduction-related volcanic arc that extends across Mexico. The crustal thickness beneath the CVF (∼50 km) is the greatest of any region in the MVB and one of the greatest found in any arc worldwide. Lavas and scoriae erupted from vents in the CVF include alkaline basalts and calc-alkaline basaltic andesites, andesites, and dacites. Both alkaline and calc-alkaline groups contain primitive varieties that have whole rock Mg#, MgO, and Ni contents, and liquidus olivine compositions (≤Fo₉₀) that are close to those expected of partial melts from mantle peridotite. Primitive varieties also show a wide range of incompatible trace element abundances (e.g. Ba 210–1080 ppm; Ce 25–100 ppm; Zr 130–280 ppm). Data for primitive calc-alkaline rocks from both the CVF and other regions of the MVB to the west are consistent with magma generation in an underlying mantle wedge that is depleted in Ti, Zr, and Nb and enriched in large ion lithophile (K, Ba, Rb) and light rare earth (La, Ce) elements. Extents of partial melting estimated from Ti and Zr data are lower for primitive calc-alkaline magmas in the CVF than for those from the regions of the MVB to the west where the crust is thinner. The distinctive major element compositions (low CaO and Al₂O₃, high SiO₂) of the primitive calc-alkaline magmas in the CVF indicate a more refractory mantle source beneath this region of thick crust. In contrast, primitive alkaline magmas from the CVF and other regions of the MVB show compositional similarities to intraplate-type alkali basalts erupted behind the arc in the Mexican Basin and Range province. These similarities are consistent with the hypothesis that slab-induced convection in the mantle wedge beneath the MVB causes advection of asthenospheric mantle from behind the arc to the region of magma generation. Trace element systematics of primitive magmas in the MVB reveal substantial variability in both the extent of mantle wedge enrichment by subduction processes and in the composition of mantle heterogeneities that are related to previous extraction of alkaline to sub-alkaline basaltic melts. Received: 23 June 1998 / Accepted: 23 December 1998     

Absarokites from the western Mexican Volcanic Belt: constraints on mantle wedge conditions

We have investigated the near liquidus phase relations of a primitive absarokite from the Mascota region in western Mexico. Sample M.102 contains ~11.6 wt% MgO, Mg#=0.73 and the lava contains Fo₉₀ olivine phenocrysts, indicating near equilibrium with the mantle. High-pressure experiments on a synthetic analogue of the absarokite composition containing low and high H₂O abundances of (~2 and ~5 wt%, respectively) were performed in a piston cylinder apparatus over the pressure range of 1.2 to 2.0 GPa. The composition containing ~2 wt% H₂O is multiply saturated with olivine and orthopyroxene at 1.6 GPa and 1,400 °C. At the same pressure, clinopyroxene appears 30 °C below the liquidus. At an H₂O content of ~5 wt% the multiple saturation with olivine and orthopyroxene occurs at 1.7 GPa and 1,300 °C. Assuming a batch-melting process, we suggest that the primitive absarokite was segregated from a depleted lherzolite or harzburgite residue at ~50 km, placing the depth of origin well within the mantle wedge beneath the Jalisco Block. A low degree (<5 %wt%) batch-melt of an original metasomatized depleted lherzolite or harzburgite source would contain the observed trace element abundances found in M.102. The liquidus phase relations are not consistent with the presence of non-peridotitic veins at the depth of last equilibration. Therefore, we propose that the Mascota absarokites segregated at an apparent melt fraction of less than 5% from a depleted peridotitic source. Melting first began at a greater depth as a small degree H₂O- and trace element- rich melt of a metasomatized peridotite that ascended into the overlying wedge and re-equilibrated with shallower, hotter mantle.Editorial responsibility: J. Hoefs     

Quaternary minettes and associated volcanic rocks of Mascota,western Mexico: a consequence of plate extension above a subduction modified mantle wedge

 Pleistocene-Holocene volcanism in the Jalisco block of western Mexico is confined to two conspicuous grabens, where potassic eruptives range from absarokites (48–52% SiO₂) and minettes (49–54% SiO₂) through basaltic andesites (53–57% SiO₂), the most voluminous type, to andesites and their lamprophyric equivalent spessartite (58–62% SiO₂); there are no contemporary rhyolitic rocks. This suite has high concentrations of Mg, Cr (<550 ppm) and Ni (<450 ppm) accompanied by large concentrations of K, P, Ba (<4000 ppm) and Sr (<5000 ppm) and elements such as LREE and Zr (<600 ppm). No combination of crystal fractionation and/or crustal contamination can reproduce the compositional range of these magmas, which nevertheless are believed to be genetically related because of their proximity in time and space. Hydrous minerals in the lamprophyres and the typical absence of plagioclase phenocrysts in both basaltic andesites and andesites reflect the relatively high concentrations of water in the magmas, which suppressed the crystallisation of feldspar. Experimental verification of the minimal amounts of water required to reproduce the phenocryst assemblages in selected rocks range from 3.5 to 6%. During ascent in a volcanic conduit, andesitic magma may lose water and consequently precipitate plagioclase, or it may ascend more rapidly, retaining more of its initial water, which stabilises phenocrysts of hornblende at the expense of plagioclase. Our estimates of water concentrations, which are consistent with the various low pressure phenocryst assemblages, will be minimal for the magmas in their source regions, and the process of magmatic dewatering on ascent may be typical in well established volcanic conduits. In accord with the compositions of phenocrystic olivine in the basaltic andesites and the minettes, the values of FeO and Fe₂O₃ of the bulk lavas and scoriae are demonstrably pristine. As a consequence, there are two characteristic features of the Mascota suite: the high range of relative oxygen fugacities (ΔNNO=1–5) and the high Mg# (MgO/MgO+FeO) that ranges from 0.70 to 0.91 (with only one andesite as low as 0.66). From the evidence of phlogopite phenocrysts, a partial melt involving phlogopite would have a higher Mg# than one from olivine (Fo₉₀) and pyroxene alone. As the Mascota series shows a correlation between K₂O and Mg#, we conclude that it was generated by partial fusion of the mantle wedge, with a variable contribution of phlogopite and apatite from veins throughout the lherzolitic assemblage. In conformity with an origin by varying increments of partial fusion of a phlogopite-bearing mantle, all incompatible elements vary linearly with Ti (or K) as if phlogopite (+apatite) in the source dominated their contribution to the partial melts. Fluids from dehydration of the subducting slab presumably deposit hydrous and other minerals in veins in the mantle wedge and also increase its redox state. As the Mascota volcanism occurs in grabens closer to the trench than the main andesite arc, it is concluded that the eruption of these small volumes of hydrous magmas require the tectonically favored ascent paths offered by the extensional grabens to reach the surface from their mantle sources. Received: 24 January 1995 / Accepted: 21 February 1996     

The role of slab melting in the petrogenesis of high-Mg andesites: evidence from Simbo Volcano,Solomon Islands

The petrogenesis of high-Mg andesites (HMA) in subduction zones involves shallow melting of refractory mantle sources or, alternatively, the interaction of ascending slab-derived melts with mantle peridotite. To unravel the petrogenesis of HMA, we report major, trace element and Sr–Nd–Hf–Pb isotope data for a newly found occurrence of HMA in the New Georgia group, Solomon Islands, SW-Pacific. Volcanism in the Solomon Islands was initiated by subduction of the Pacific plate beneath the Indian–Australian plate until a reversal of subduction polarity occurred ca. 10 Ma ago. Currently, the Indian–Australian plate is subducted northeastwards along the San Cristobál trench, forming the younger and still active southwestern Solomon island arc. However, a fossil slab of Pacific crust is still present beneath the arc. The edifice of the active volcano Simbo is located directly in the San Cristobál trench on top of the subducting Indian–Australian plate. Simbo Island lies on top of a strike-slip fault of the adjacent Woodlark spreading centre that is subducted beneath the Pacific plate. Geochemical and petrological compositions of volcanic rocks from Simbo are in marked contrast to those of volcanic rocks from islands north of the trench (mostly arc basalts). Simbo-type rocks are opx-bearing HMA, displaying 60–62 wt% SiO₂ but rather primitive Mg–Ni–Cr characteristics with 4–6 wt% MgO, up to 65 ppm Ni, up to 264 ppm Cr and Mg# from 67 to 75. The compositions of the Simbo andesites are explained by a binary mixture of silicic and basaltic melts. Relict olivine phenocrysts with Fo_88–90 and reaction-rims of opx also support a mixing model. The basaltic endmember is similar to back-arc basalts from the Woodlark Ridge. A slab melt affinity of the silicic mixing component is indicated by Gd_(N)/Yb_(N) of up to 2.2 that is higher if compared to MORB and other arc basalts from the Solomon Islands. ⁸⁷Sr/⁸⁶Sr, ɛNd and ɛHf values in the analysed rocks range from 0.7035 to 0.7040, +6.4 to +7.9 and +12 to +14.4, respectively. These values reveal the presence of the Indian–Australian mantle domain beneath Simbo (i.e. the Indian–Australian plate) and also beneath all other volcanic islands of the New Georgia group, which are located north of the San Cristobál trench. ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb values (18.43–18.52, 15.49–15.55 and 18.13–18.34, respectively) confirm the presence of slab melts from the subducted Pacific plate beneath southern Simbo where the highest Gd_(N)/Yb_(N) ratios are reported. A spatial shift towards an Indian–Australian slab signature is observed when approaching the active San Cristobál trench on northern Simbo, reflecting the decreasing influence of slab melts from the old subducted Pacific plate.     

Hydrous peridotites with Ti-rich chromian spinel as a low-temperature forearc mantle facies: evidence from the Happo-O’ne metaperidotites (Japan)

The Happo-O’ne peridotite complex is situated in the northeastern part of the Hida Marginal Tectonic Zone, central Japan, characterized by the high-P/T Renge metamorphism, and is considered as a serpentinite mélange of Paleozoic age. Peridotitic rocks, being massive or foliated, have been subjected to hydration and metamorphism. Their protoliths are mostly lherzolites to harzburgites with subordinate dunites. We found a characteristic mineral assemblage, olivine + orthopyroxene + tremolite + chlorite + chromian spinel, being stable at low-T, from 650 to 750°C, and high-P, from 16 to 20 kbar, tremolite–chlorite peridotites of the tremolite zone. Olivines are Fo₈₈–Fo_91, and orthopyroxenes (Mg# = 0.91) show low and homogenous distributions of Al₂O₃ (up to 0.25 wt%), Cr₂O₃ (up to 0.25 wt%), CaO (up to 0.36 wt%) and TiO₂ (up to 0.06 wt%) due to the low equilibration temperature. Chromian spinels, which are euhedral and enclosed mainly in the orthopyroxenes, have high TiO_2, 3.1 wt% (up to 5.7 wt%) on average, and high Cr# [=Cr/(Cr + Al) atomic ratio], 0.95 on average but low Fe³⁺ [=Fe³⁺/(Cr + Al + Fe³⁺) atomic ratio, <0.3]. The bulk-rock chemistry shows that the Happo-O’ne metaperidotites with this peculiar spinel are low in TiO₂ (0.01–0.02 wt%), indicating no addition of TiO₂ from the outside source during the metamorphism; the high TiO₂ of the peculiar spinel has been accomplished by Ti release from Ti-bearing high-T pyroxenes during the formation of low-T, low-Ti silicates (<0.1 wt% TiO₂) during cooling. Some dunites are intact from hydration: their olivine is Fo₉₂ and spinel shows high Cr#, 0.72. The Happo-O’ne metaperidotites (tremolite–chlorite peridotites), being in the corner of the mantle wedge, are representative of a hydrous low-T, high-P mantle peridotite facies transitional from a higher T anhydrous peridotite facies (spinel peridotites) formed by in situ retrograde metamorphism influenced by fluids from the subducting slab. They have suffered from low-T (<600°C) retrogressive metamorphism to form antigorite and diopside during exhumation of the Renge metamorphic belt.     

The hydrous phase equilibria (to 3 kbar) of an andesite and basaltic andesite from western Mexico: constraints on water content and conditions of phenocryst growth

We have conducted high pressure (to 3 kbar), water saturated melting experiments on an andesite (62 wt% SiO₂) and a basaltic andesite (55 wt% SiO₂) from western Mexico. A close comparison between the experimental phase assemblages and their compositions, and the phenocryst assemblages of the lavas, is found in water saturated liquids, suggesting that the CO₂ content was minimal in the fluid phase. Thus the historic lavas from Volcan Colima (with phenocrysts of orthopyroxene, augite, plagioclase, and hornblende) were stored at a temperature between 950–975 °C, at a pressure between 700–1500 bars, and with a water content of 3.0–5.0 wt%. A hornblende andesite (spessartite) from Mascota, of nearly identical composition but with only amphibole phenocrysts, had a similar temperature but equilibrated at a minimum of 2000 bars pressure with a dissolved water content of at least 5.5 wt% in the liquid. Experiments on the basaltic andesite show that the most common natural phenocryst assemblages (olivine, ±augite, ±plagioclase) could have precipitated at temperatures from 1000–1150 °C, in liquids with a wide range of dissolved water content (∼2.0–6.0 wt%) and a corresponding pressure range. A lava of the same bulk composition with phenocrysts of hornblende, olivine, plagioclase, and augite is restricted to temperatures below 1000 °C and pressures below 2500 bars, corresponding to <5.5 wt% water in the residual liquid. Although there is some evidence for mixing in the andesites (sporadic olivine phenocrysts), the broad theme of the history of both lava types is that the phenocryst assemblages for both the andesitic magmas and basaltic andesitic magmas are generated from degassing and reequilibration on ascent of initially hydrous parents containing greater than 6 wt% water. Indeed andesitic magmas could be related to a basaltic andesite parent by hornblende-plagioclase fractionation under the same hydrous conditions. Received: 10 December 1996 / Accepted: 21 August 1997     

Mineralogy and proposed P-T paths of basaltic lavas from Rabaul caldera,Papua New Guinea

Rabaul caldera is a large volcanic depression at the north-east tip of New Britain, Papua New Guinea. The lavas range in composition from basalt to rhyolite and have a calc-alkalic affinity but also display features typical of tholeiites, including moderate absolute iron enrichment in flows cropping out around the caldera. The basalts contain phenocrysts of plagioclase and clinopyroxene with less abundant olivine and titanomagnetite. In the basaltic andesites olivine is rare, while orthopyroxene and titanomagnetite are common along with plagioclase and clinopyroxene. Orthopyroxene is also found mantling olivine in some of the basalts while in both rock types pigeonitic augite is a fairly common constituent of the groundmass. Plagioclase in both basalt and basaltic andesite often exhibits sieve texture and analysis of the glass blebs show them to be of similar composition to the bulk rock. Phenocrystic clinopyroxene is a diopsidic augite in both basalt and basaltic andesite. Al₂O₃ content of the clinopyroxene is moderately high (4%) and often shows considerable variation in any one grain. Calculations show that the microphenocrysts probably crystallised near the surface, while phenocrysts crystallised at around 7 kb (21 km). Neither the basalts nor the basaltic andesites would have been in equilibrium at any geologically reasonable P and T with quartz eclogite. Equilibration between mantle peridotite and a. typical Rabaul basaltic liquid could have occurred around 35 kb and 1270 °C. A basaltic andesite liquid yields a temperature of 1263 °C and a pressure of 28 kb for equilibration with mantle peridotite.Partial melting of sufficient volumes of mantle peridotite at these P's and T's requires about 15% H₂O, but there is no evidence that these magmas ever contained large amounts of water. It is proposed that the Rabaul magmas were initially generated by partial melting of subducted lithosphere and subsequently modified by minor partial melting as they passed through the overlying mantle peridotite.     

Experimental study of the phase and melting relations of homogeneous basalt + peridotite mixtures and implications for the petrogenesis of flood basalts

Flood basalt provinces may constitute some of the most catastrophic volcanic events in the Earth's history. A popular model to explain them involves adiabatic ascent of plumes of anomalously hot peridotite from a thermal boundary layer deep in the mantle, across the peridotite solidus. However, peridotitic plumes probably require unreasonably high potential temperatures to generate sufficient volumes of magma and high enough melting rates to produce flood volcanism. This lead to the suggestion that low melting eclogitic or pyroxenitic heterogeneities may be present in the source regions of the flood basalts. In order to constrain petrogenetic models for flood basalts generated in this way, an experimental investigation of the melting relations of homogeneous peridotite + oceanic basalt mixtures has been performed. Experiments were conducted at 3.5 GPa on a fertile peridotite (MPY90)–oceanic basalt (GA1) compositional join. The hybrid basalt + peridotite compositions crystallised garnet lherzolite at subsolidus temperatures plus quenched ne-normative picritic liquids at temperatures just above the solidus, over the compositional range MPY90 to GA1₅₀MPY90₅₀. The solidus temperature decreased slightly from ∼1500 °C for MPY90 to ∼1450 °C for GA1₅₀MPY90₅₀. Compositions similar to GA1₃₀MPY90₇₀ have 100% melting compressed into a melting interval which is approximately 50–60% smaller than that for pure MPY90, due to a liquidus minimum. During adiabatic ascent of hybrid source material containing a few tens of percent basalt in peridotite, the lower solidus and compressed solidus–liquidus temperature interval may conspire to substantially enhance melt productivity. Mixtures of recycled oceanic crust and peridotite in mantle plumes may therefore provide a viable source for some flood volcanics. Evidence for this would include higher than normal Fe/Mg values in natural primary liquids, consistent with equilibration with more Fe-rich olivine than normal pyrolitic olivine (i.e. <Fo_89–92). Modelling of fractionation trends in West Greenland picrites is presented to demonstrate that melts parental to the Greenland picrites were in equilibrium at mantle P–T conditions with olivine with Fo_84–86, suggesting an Fe-enriched source compared with normal peridotite, and consistent with the presence of a basaltic component in the source. Received: 29 October 1999 / Accepted: 3 February 2000     

Cumulate xenoliths from St. Vincent, Lesser Antilles Island Arc: a window into upper crustal differentiation of mantle-derived basalts

In order to shed light on upper crustal differentiation of mantle-derived basaltic magmas in a subduction zone setting, we have determined the mineral chemistry and oxygen and hydrogen isotope composition of individual cumulus minerals in plutonic blocks from St. Vincent, Lesser Antilles. Plutonic rock types display great variation in mineralogy, from olivine–gabbros to troctolites and hornblendites, with a corresponding variety of cumulate textures. Mineral compositions differ from those in erupted basaltic lavas from St. Vincent and in published high-pressure (4–10 kb) experimental run products of a St. Vincent high-Mg basalt in having higher An plagioclase coexisting with lower Fo olivine. The oxygen isotope compositions (δ¹⁸O) of cumulus olivine (4.89–5.18‰), plagioclase (5.84–6.28‰), clinopyroxene (5.17–5.47‰) and hornblende (5.48–5.61‰) and hydrogen isotope composition of hornblende (δD = −35.5 to −49.9‰) are all consistent with closed system magmatic differentiation of a mantle-derived basaltic melt. We employed a number of modelling exercises to constrain the origin of the chemical and isotopic compositions reported. δ¹⁸O_Olivine is up to 0.2‰ higher than modelled values for closed system fractional crystallisation of a primary melt. We attribute this to isotopic disequilibria between cumulus minerals crystallising at different temperatures, with equilibration retarded by slow oxygen diffusion in olivine during prolonged crustal storage. We used melt inclusion and plagioclase compositions to determine parental magmatic water contents (water saturated, 4.6 ± 0.5 wt% H₂O) and crystallisation pressures (173 ± 50 MPa). Applying these values to previously reported basaltic and basaltic andesite lava compositions, we can reproduce the cumulus plagioclase and olivine compositions and their associated trend. We conclude that differentiation of primitive hydrous basalts on St. Vincent involves crystallisation of olivine and Cr-rich spinel at depth within the crust, lowering MgO and Cr₂O₃ and raising Al₂O₃ and CaO of residual melt due to suppression of plagioclase. Low density, hydrous basaltic and basaltic andesite melts then ascend rapidly through the crust, stalling at shallow depth upon water saturation where crystallisation of the chemically distinct cumulus phases observed in this study can occur. Deposited crystals armour the shallow magma chamber where oxygen isotope equilibration between minerals is slowly approached, before remobilisation and entrainment by later injections of magma.     

The origin of hydrous,high-δ<Superscript>18</Superscript>O voluminous volcanism: diverse oxygen isotope values and high magmatic water contents within the volcanic record of Klyuchevskoy volcano,Kamchatka, Russia

Klyuchevskoy volcano, in Kamchatka’s subduction zone, is one of the most active arc volcanoes in the world and contains some of the highest δ¹⁸O values for olivines and basalts. We present an oxygen isotope and melt inclusion study of olivine phenocrysts in conjunction with major and trace element analyses of ¹⁴C- and tephrochronologically-dated tephra layers and lavas spanning the eruptive history of Klyuchevskoy. Whole-rock and groundmass analyses of tephra layers and lava samples demonstrate that both high-Mg (7–12.5 wt% MgO) and high-Al (17–19 wt% Al₂O₃, 3–6.5 wt% MgO) basalt and basaltic andesite erupted coevally from the central vent and flank cones. Individual and bulk olivine δ¹⁸O range from normal MORB values of 5.1‰ to values as high as 7.6‰. Likewise, tephra and lava matrix glass have high-δ¹⁸O values of 5.8–8.1‰. High-Al basalts dominate volumetrically in Klyuchevskoy’s volcanic record and are mostly high in δ¹⁸O. High-δ¹⁸O olivines and more normal-δ¹⁸O olivines occur in both high-Mg and high-Al samples. Most olivines in either high-Al or high-Mg basalts are not in oxygen isotopic equilibrium with their host glasses, and Δ¹⁸O_{olivine–glass} values are out of equilibrium by up to 1.5‰. Olivines are also out of Fe–Mg equilibrium with the host glasses, but to a lesser extent. Water concentrations in olivine-hosted melt inclusions from five tephra samples range from 0.4 to 7.1 wt%. Melt inclusion CO₂ concentrations vary from below detection (<50 ppm) to 1,900 ppm. These values indicate depths of crystallization up to ~17 km (5 kbar). The variable H₂O and CO₂ concentrations likely reflect crystallization of olivine and entrapment of inclusions in ascending and degassing magma. Oxygen isotope and Fe–Mg disequilibria together with melt inclusion data indicate that olivine was mixed and recycled between high-Al and high-Mg basaltic melts and cumulates, and Fe–Mg and δ¹⁸O re-equilibration processes were incomplete. Major and trace elements in the variably high-δ¹⁸O olivines suggest a peridotite source for the parental magmas. Voluminous, highest in the world with respect to δ¹⁸O, and hydrous basic volcanism in Klyuchevskoy and other Central Kamchatka depression volcanoes is explained by a model in which the ascending primitive melts that resulted from the hydrous melt fluxing of mantle wedge peridotite, interacted with the shallow high-δ¹⁸O lithospheric mantle that had been extensively hydrated during earlier times when it was part of the Kamchatka forearc. Following accretion of the Eastern Peninsula terrains several million years ago, a trench jump eastward caused the old forearc mantle to be beneath the presently active arc. Variable interaction of ascending flux-melting-derived melts with this older, high-δ¹⁸O lithospheric mantle has produced mafic parental magmas with a spectrum of δ¹⁸O values. Differentiation of the higher δ¹⁸O parental magmas has created the volumetrically dominant high-Al basalt series. Both basalt types incessantly rise and mix between themselves and with variable in δ¹⁸O cumulates within dynamic Klyuchevskoy magma plumbing system, causing biannual eruptions and heterogeneous magma products. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Experimental constraints on the origins of primitive potassic lavas from the Trans-Mexican Volcanic Belt

Primitive magmas in the Trans-Mexican Volcanic Belt (TMVB) span a wide geochemical range that includes calc-alkaline basalt and basaltic andesite, potassic shoshonites, and intraplate alkaline basalts, indicating that the subarc mantle wedge is chemically heterogeneous. The aim of this study is to experimentally constrain the origins of potassic lavas that have erupted along the volcanic front in the TMVB. We used a piston-cylinder apparatus to determine the P–T–H₂O near-liquidus phase relations for two primitive potassic lavas: a hornblende trachybasalt (shoshonite) from Cerro La Pilita in the central TMVB and a high-K calc-alkaline basalt from Ayutla in the western TMVB. Experiments were conducted at mantle pressures (0.8–2.5 GPa) and temperatures (1,100–1,400 °C) with 1.5–6 wt% H₂O. Results show that both samples were last equilibrated with an olivine + clinopyroxene assemblage at upper mantle pressures. Integrating our results with trace element characteristics, we conclude that the potassic magmas formed by a complex, multistage process in which melts from the hottest part of the mantle wedge either reequilibrated with clinopyroxene-rich veins in the shallow upper mantle or caused melting of such veins by advective heating. We combine our results with previous experiments on TMVB lavas to provide an along-arc perspective of melt equilibration depths in the mantle wedge. The results suggest that although melts may initially form deep in the wedge, they commonly reequilibrate with heterogeneous mantle at shallower depths. Primitive, medium-K basaltic andesites in the TMVB form by reequilibration with harzburgite, which we infer to be a common lithology in the upper mantle, whereas some potassic magmas like the ones studied here form through reequilibration with or melting of veins of olivine + clinopyroxene ± phlogopite. Though somewhat rare at the volcanic front relative to the more abundant medium-K volcanic rocks, the potassic magmas are an important lava type for revealing mantle chemical heterogeneities.     

Silicic melts produced by reaction between peridotite and infiltrating basaltic melts: ion probe data on glasses and minerals in veined xenoliths from La Palma, Canary Islands

Mantle xenoliths hosted by the historic Volcan de San Antonio, La Palma, Canary Islands include veined spinel harzburgites and spinel dunites. Glasses and associated minerals in the vein system of veined xenoliths show a gradual transition in composition from broad veins to narrow veinlets. Broad veins contain alkali basaltic glass with semi-linear trace element patterns enriched in strongly incompatible elements. As the veins become narrower, the SiO₂-contents in glass increase (46 → 67 wt% SiO₂ in harzburgite, 43 → 58 wt% in dunite) and the trace element patterns change gradually to concave patterns depleted in moderately incompatible elements (e.g. HREE, Zr, Ti) relative to highly incompatible ones. The highest SiO₂-contents (ca. 68% SiO₂, low Ti-Fe-Mg-Ca-contents) and most extreme concave trace element patterns are exhibited by glass in unveined peridotite xenoliths. Clinopyroxenes shift from LREE-enriched augites in basaltic glass, to REE-depleted Cr-diopside in highly silicic glass. Estimates indicate that the most silicic glasses represent melts in, or near, equilibrium with their host peridotites. The observed trace element changes are compatible with formation of the silicic melts by processes involving infiltration of basaltic melts into mantle peridotite followed by reactions and crystallization. The Fe-Mg interdiffusion profiles in olivine porphyroclasts adjacent to the veins indicate a minimum period of diffusion of 600 years, implying that the reaction processes have taken place in situ in the upper mantle. The CaO-TiO₂-La/Nd relationships of mantle rocks may be used to discriminate between metasomatism caused by carbonatitic and silicic melts. Unveined mantle xenoliths from La Palma and Hierro (Canary Islands) show a wide range in La/Nd ratios with relatively constant, low-CaO contents which is compatible with metasomatism of “normal” abyssal peridotite by silicic melts. Peridotite xenoliths from Tenerife show somewhat higher CaO and TiO₂ contents than those from the other islands and may have been affected by basaltic or carbonatitic melts. The observed trace element signatures of ultramafic xenoliths from La Palma and other Canary Islands may be accounted for by addition of small amounts (1–7%) of highly silicic melt to unmetasomatized peridotite. Also ultramafic xenoliths from other localities, e.g. eastern Australia, show CaO-TiO₂-La/Nd relationships compatible with metasomatism by silicic melts. These results suggest that silicic melts may represent important metasomatic agents. Received: 15 November 1998 / Accepted: 17 May 1999     

Contemporaneous eruption of calc-alkaline and alkaline lavas in a continental arc (Eastern Mexican Volcanic Belt): chemically heterogeneous but isotopically homogeneous source

Nearly contemporaneous eruption of alkaline and calc-alkaline lavas occurred about 900 years BP from El Volcancillo paired vent, located behind the volcanic front in the Mexican Volcanic Belt (MVB). Emission of hawaiite (Toxtlacuaya) was immediately followed by calc-alkaline basalt (Río Naolinco). Hawaiites contain olivine microphenocrysts (Fo_67–72), plagioclase (An_56–60) phenocrysts, have 4–5 wt% MgO and 49.6–50.9 wt% SiO₂. In contrast, calc-alkaline lavas contain plagioclase (An_64–72) and olivine phenocrysts (Fo_81–84) with spinel inclusions, and have 8–9 wt% MgO and 48.4–49.4 wt% SiO₂. The most primitive lavas in the region (Río Naolinco and Cerro Colorado) are not as primitive as parental melts in other arcs, and could represent either (a) variable degrees of melting of a subduction modified, garnet-bearing depleted mantle source, followed by AFC process, or (b) melting of two distinct mantle sources followed by AFC processes. These two hypotheses are evaluated using REE, HFSE, and Sr, Os and Pb isotopic data. The Toxtlacuaya flow and the Y & I lavas can be generated by combined fractional crystallization and assimilation of gabbroic granulite, starting with a parental liquid similar to the Cerro Colorado basalt. Although calc-alkaline and alkaline magmas commonly occur together in other areas of the MVB, evidence for subduction component in El Volcancillo magmas is minimal and limited to <1%, which is a unique feature in this region further from the trench. El Volcancillo lavas were produced from two different magma batches: we surmise that the injection of calc-alkaline magma into an alkaline magma chamber triggered the eruption of hawaiites. Our results suggest that the subalkaline and hawaiitic lavas were formed by different degrees of partial melting of a similar, largely depleted mantle source, followed by later AFC processes. This model is unusual for arcs, where such diversity is usually explained by melting of heterogeneous (enriched and depleted) and subduction-modified mantle.     

Magnesian andesites in north Xinjiang,China

Middle Devonian magnesian andesites (MAs) are widely distributed in south Altay and Carboniferous MAs are present in Alataoshan and west- and east-Tianshan in the north Xinjiang region. These MAs are andesitic rocks with 53–65% SiO₂,<1% (0.21–1.08%; average of 0.72%) TiO₂, and ≥50 Mg^#. Magnesian dacites and diorites, with 52.38–66.91% SiO₂, <0.30% TiO₂ and ≥42 Mg^# commonly occur with these MAs. Relative to boninites, MAs have lower MgO contents (average 6.39%) but higher Ti, K and Na. They have characteristic flat chondrite-normalized REE patterns with weak to no Eu anomalies (Eu depletion, or Eu/Eu* = 0.65–1.15), low (La/Yb)_N (0.98–6.4, mostly 4±) and low total REE contents (15–95 ppm). They also have high contents of compatible elements Cr and Ni (72–790 and 29–276 ppm, respectively). Their relative depletion in high field strength elements Nb, Ta and Ti, and relative enrichment in mobile large-ion lithophile elements Rb, K and Pb are evident on primitive mantle-normalized trace element spidergrams. If magnesian andesites are melts coming from the subducted oceanic crust, as proposed elsewhere, then the relatively high Y contents (>15 ppm), low Sr/Y ratios (4.4–6.2), low (La/Yb)N, and high Mg^# of the MAs in north Xinjiang provide evidence of interaction of such melts with mantle wedge peridotite. New petrographic, chemical and isotopic [(¹⁴³Nd/¹⁴⁴Nd)I = 0.51221–0.51255 (εNd(t) +0.28 to +7.2); (⁸⁷Sr/⁸⁶Sr)I = 0.7029–0.7065] data suggest that the petrogenesis of the MAs in the north Xinjiang region may have involved: (1) multiple source materials including subducted oceanic slab, juvenile crustal materials (mainly volcanic-volcanoclassic rocks with low maturity and clear mantle geochemical signatures) coming from the forearc accretionary prism and mantle wedge peridotite; (2) a combination of different petrogenetic processes including partial melting of subducted oceanic slab and juvenile crustal materials, followed by interaction of slab melts with the mantle wedge peridotite; (3) high geothermal gradient creating a high temperature (>1,000°C) environment in a volatile-rich source region; (4) unique tectonic settings including oblique subduction, slab break off resulting in slab window formation and asthenosphere upwelling, and subduction erosion resulting in transfer of forearc accretionary materials into the source region of MA magma.