Magma mingling in the ∼50 ka Rotoiti eruption from Okataina Volcanic Centre: implications for geochemical diversity and chronology of large volume rhyolites

Examination of glass and crystal chemistry in the Rotoiti Pyroclastics (>100 km³ of magma) demonstrates that compositional diversity was produced by mingling of the main rhyolite magma body with small volumes of other magmas that had been crystallizing in separate stagnant magma chambers. Most (>90%) of the Rotoiti deposits were derived from a low-K₂O, cummingtonite-bearing, rhyolitic magma (T1) discharged throughout the eruption sequence. T1 magma is homogeneous in composition (melt SiO₂=77.80±0.28 wt.%), temperature (766±13 °C) and oxygen fugacity (NNO+0.92±0.09). Most T1 phenocrysts formed in a shallow (∼200 MPa), near water-saturated (a_water=0.8) storage chamber shortly before eruption. Basaltic scoria erupted immediately before the rhyolites, and glass-bearing microdiorite inclusions within the rhyolite deposits, suggest that basalt emplaced on the floor of the chamber drove vigorous convection to produce the well-mixed T1 magma. Lithic lag breccias contain melt-bearing biotite granitoid inclusions that are compositionally distinct from T1 magma. The breccias which overlie the voluminous T1 pyroclastic flow deposits resulted from collapse of the syn-Rotoiti caldera. Post-collapse Rotoiti pumices contain T1 magma mingled with another magma (T2) that is characterized by high-K glass and biotite, and was cooler and less oxidised (712±16 °C; NNO−0.16±0.16). The mingled clasts contain bimodal disequilibrium populations of all crystal phases. The granitoid inclusions and the T2 magma are interpreted as derived from high-K magma bodies of varying ages and states of crystallization, which were adjacent to but not part of the large T1 magma body. We demonstrate that these high-K magmas contaminated the erupting T1 magma on a single pumice clast scale. This contamination could explain the reported wide range of zircon U–Th ages in Rotoiti pumices, rather than slow crystallization of a single large magma body.     

Ultramafic inclusions in anorthite megacrysts from the Isle of Skye

1–15 μm diameter ultramafic inclusions in anorthitic plagioclase megacrysts from Skye were analyzed by electron microprobe and tentatively identified as sub-calcic augite, or sub-calcic augite submicroscopically intergrown with amphibole. The inclusions nucleated in Ca-Al-depleted, Fe-Mg-H₂O-enriched magma adjacent to the interface between plagioclase crystals and basalt and were rapidly enveloped by the growing plagioclase. The inclusions may be important in the fractional crystallization of the Skye alkali olivine basalt suite.     

Megacrysts in the Cenozoic basalt of the Tuoyun Basin,Southwest Tianshan

Abundant megacrysts of clinopyroxene, amphibole, anorthoclase, and phlogopite are found together with deep-seated xenoliths in the Cenozoic basalt of the Tuoyun Basin, Southwest Tianshan. The megacrysts are mainly in the cone sheet formed at the early stage of the volcanic activity. Clinopyrox-ene megacrysts are located in the lower part of the profile, with amphibole and phlogopite megacrysts in the middle part and anorthoclase megacrysts in the upper part. The crystal integrity, absence of de-formation fabric and their relation to the host basalt suggest that they were crystallized from the host magma and quickly transported to the surface. The mineralogical studies imply that the clinopyroxene megacrysts are of Al-augite with higher Al2O3 (>9%). Amphibole megacrysts are kaersutite rich in TiO2 (>4.5%). Sulfide inclusions such as pyrrhotite occur in some clinopyroxene and amphibole megacrysts. Thermodynamic calculations reveal that pyroxene megacrysts formed under the temperature of 1185.85―1199.85℃ and the pressure between 1.53 and 1.64 GPa comparable to the crust-mantle boundary and amphibole megacrysts crystallized under the pressure of around 0.85 GPa, temperature about 1000℃ comparable to the depth of 30 km. Anorthoclase megacrysts crystallized under the pressure between 0.8―1 GPa,temperature about 900℃.The absence of Ti-rich inclusions such as rutile can be considered as an evidence of quick magma ascending. The P-T conditions estimated via py-roxene megacrysts and phenocrysts compose a P-T path with a steep slope. It can be considered as another evidence of quick magma ascending. However, the estimated temperatures for amphibole megacrysts are markedly lower than those for pyroxene megacrysts given the same pressure. It probably shows that the amphiboles have crystallized at the vanguard of magma and under the vola-tile-rich condition. Thus, we can conclude that the Cenozoic basalts are produced in an extensional tectonic setting and the processes governing crystallization and ascending of the megacrysts are very complex.     

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.     

Silicate systems bearing on the crystallization courses in alkali basalts

Phase-equilibrium studies of the nepheline normative portion of the basalt tetrahedron nepheline-forsterite-silica-diopside ofYoder andTilley have shown that during the course of crystallization the composition of the liquid phase leaves this tetrahedron. When the tetrahedron is expanded to nepheline-forsterite-silica-Ca₂SiO₄ the courses of crystallization and composition of the liquid can be and have been followed by studying a series of joins within this expanded tetrahedron. These studies show that the ultimate goal of crystallization is the quaternary invariant point diopsidic pyroxene + nepheline solid solution + sodic plagioclase + wollastonite solid solution + liquid at 950 ± 5°"C. Attention is called to this low melting point in a dry system. With perfect equilibrium between the solid phases and liquid all melilite disappears by reaction with liquid below 1065 ± 5°C, the temperature of the quaternary reaction point with diopsidic pyroxene + melilite + nepheline solid solution + wollastonite solid solution + liquid. A flow sheet showing the reactions between all quaternary invariant points in the geologically interesting portion of the expanded tetrahedron is presented. This shows the interrelations (daughter-parent relations) between a large number of rock types found in intrusive and extrusive nepheline normative compositions as well as in the quartz normative tholeiitic basalts.     

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.     

Potassium enrichment by magma mixing and vapor exsolution: an example in the miocene volcanism of eastern Morocco

Miocene volcanism in eastern Morocco is comprised of potash rich calc-alkalic and alkaline rocks. In the southern part of the area, at the base of the Guilliz massif, basic inclusions are found in latites. From a petrological, geochemical and mineralogical study of both latites and their inclusions, it appear that the inclusions represent a basic liquid quenched in the latitic magma, inside the magma chamber. As a result of the drop in pressure and crystallization, a K-rich vapour phase separated from the inclusion-forming liquid and percolated the latitic magma, increasing the K₂O content of the latter and possibly triggering eruptions. The mixing process between the two magmas seems supported by density and viscosity estimations. Calculations show that for temperatures ranging from 700 °C to 1000 °C and H₂O contents from 1.6 to 5%, the inclusion forming liquid is less dense than the latitic liquid and can therefore ascend into the latitic magma by interface disequilibrium and flotation.     

Did boninite originate from the heterogeneous mantle with recycled ancient slab?

Boninites are widely distributed along the western margin of the Pacific Plate extruded during the incipient stage of the subduction zone development in the early Paleogene period. This paper discusses the genetic relationships of boninite and antecedent protoarc basalt magmas and demonstrates their recycled ancient slab origin based on the T–P conditions and Pb–Hf–Nd–Os isotopic modeling. Primitive melt inclusions in chrome spinel from Ogasawara and Guam islands show severely depleted high‐SiO₂, MgO (high‐silica) and less depleted low‐SiO₂, MgO (low‐silica and ultralow‐silica) boninitic compositions. The genetic conditions of 1 346 °C at 0.58 GPa and 1 292 °C at 0.69 GPa for the low‐ and ultralow‐silica boninite magmas lie on adiabatic melting paths of depleted mid‐ocean ridge basalt mantle with a potential temperature of 1 430 °C in Ogasawara and of 1 370 °C in Guam, respectively. This is consistent with the model that the low‐ and ultralow‐silica boninites were produced by remelting of the residue of the protoarc basalt during the forearc spreading immediately following the subduction initiation. In contrast, the genetic conditions of 1 428 °C and 0.96 GPa for the high‐silica boninite magma is reconciled with the ascent of more depleted harzburgitic source which pre‐existed below the Izu–Ogasawara–Mariana forearc region before the subduction started. Mixing calculations based on the Pb–Nd–Hf isotopic data for the Mariana protoarc basalt and boninites support the above remelting model for the (ultra)low‐silica boninite and the discrete harzburgite source for the high‐silica boninite. Yb–Os isotopic modeling of the high‐Si boninite source indicates 18–30 wt% melting of the primitive upper mantle at 1.5–1.7 Ga, whereas the source mantle of the protoarc basalt, the residue of which became the source of the (ultra)low‐Si boninite, experienced only 3.5–4.0 wt% melt depletion at 3.6–3.1 Ga, much earlier than the average depleted mid‐ocean ridge basalt mantle with similar degrees of melt depletion at 2.6–2.2 Ga.     

Phenocryst-hosted melt inclusions record stalling of magma during ascent in the conduit and upper magma reservoir prior to vulcanian explosions, Soufrière Hills volcano, Montserrat, West Indies

The mechanics of explosive eruptions influence magma ascent pathways. Vulcanian explosions involve a stop–start mechanism that recurs on various timescales, evacuating the uppermost portions of the conduit. During the repose time between explosions, magma rises from depth and refills the conduit and stalls until the overpressure is sufficient to generate another explosion. We have analyzed major elements, Cl, S, H₂O, and CO₂ in plagioclase-hosted melt inclusions, sampled from pumice erupted during four vulcanian events at Soufrière Hills volcano, Montserrat, to determine melt compositions prior to eruption. Using Fourier transform infrared spectroscopy, we measured values up to 6.7 wt.% H₂O and 80 ppm CO₂. Of 42 melt inclusions, 81 % cluster between 2.8 and 5.4 wt.% H₂O (57 to 173 MPa or 2–7 km), suggesting lower conduit to upper magma reservoir conditions. We propose two models to explain the magmatic conditions prior to eruption. In Model 1, melt inclusions were trapped during crystal growth in magma that was stalled in the lower conduit to upper magma reservoir, and during trapping, the magma was undergoing closed-system degassing with up to 1 wt.% free vapor. This model can explain the melt inclusions with higher H₂O contents since these have sampled the upper parts of the magma reservoir. However, the model cannot explain the melt inclusions with lower H₂O because the timescale for plagioclase crystallization and melt inclusion entrapment is longer than the magma residence time in the conduit. In Model 2, melt inclusions were originally trapped at deeper levels of the magma chamber, but then lost hydrogen by diffusion through the plagioclase host during periodic stalling of the magma in the lower conduit system. In this second scenario, which we favor, the melt inclusions record re-equilibration depths within the lower conduit to upper magma reservoir.     

Rifting episode in north iceland in 1874–1875 and the eruptions of askja and sveinagja

In 1874 and 1875 the fissure swarm of Askja central volcano was activated during a major rifting episode. This rifting resulted in a fissure eruption of 0.3 km³ basaltic magma in Sveinagja graben, 50 to 70 km north of Askja and subsequent caldera collapse forming the Oskjuvatn caldera within the main Askja caldera. Five weeks after initial collapse, an explosive mixed magma eruption took place in Askja. On the basis of matching chemistry, synchronous activity and parallels with other rifted central volcanoes, the events in Askja and its lissure swarm are attributed to rise of basaltic magma into a high-level reservoir in the central volcano, subsequent rifting of the reservoir and lateral flow magma within the fissure swarm to emerge in the Sveinagja eruption. This lateral draining of the Askja reservoir is the most plausible cause for caldera collpse. The Sveinagja basalt belong to the group of evolved tholejites characteristie of several Icelandic central volcanoes and associated fissure swarms. Such tholeiites, with Mgvalues in the 40 to 50 tange, represent magmas which have suffered extensive fractional crystallization within the crust. The 12% porphyritic Sveinagja basalt contains phenocrysts of olivine (Fo_62–67), plagioclase (An_57–62), clinopyroxene (Wo₃₈En₄₆Wo₁₆) and titanomagnetite. Extrusion temperature of the lava, calculated on the basis of olivine and plagioclase geothermometry, is found to be close to 1150°C.     

Plagiogranites as late-stage immiscible liquids in ophiolite and mid-ocean ridge suites: An experimental study

Chemical studies of two ophiolite suites and of selected mid-oceanic rift (MOR) regions indicate the presence of certain magmatic compositions: basalt, Fe-enriched basalt, and sodium granite (plagiogranite). There is a notable lack of evidence for melts of intermediate composition (i.e. 50–60 wt.% SiO₂). To determine possible relationships between basic rocks (basalts and gabbros) and acidic rocks (plagiogranites) a primitive basalt was fractionated at low pressure, under anhydrous conditions, and at different oxygen fugacities near the iron-wustite buffer and slightly above the quartz-fayalite-magnetite buffer. Samples of this basalt were taken to slightly above liquidus temperatures and then cooled at rates ranging from 1 to 2°C/hr. A liquid line of descent characterized by an Fe enrichment was delineated by quenching these experiments from a final temperature in the range of 1200 to 1000°C and analyzing the residual liquid (glass). After 95% crystallization of olivine, plagioclase, calcium pyroxene, and ilmenite, the residual liquid was an Fe-enriched basalt. This Fe-enriched basalt became immiscible at a temperature of about 1010°C. The immiscible phases produced were a more Fe-enriched basaltic liquid and a granitic liquid. The granitic liquid is similar in composition to the naturally occurring plagiogranites found in small volumes in ophiolites and in certain MOR regions. It is therefore concluded that silicate liquid immiscibility could be the petrogenetic process responsible for producing plagiogranite in some MOR regions and in some ophiolites. On the other hand, plagiogranites in ophiolites and MOR rock suites having andesitic and dacitic composition rocks may have evolved under conditions more closely approximating equilibrium crystallization and/or they may have evolved at high water pressures. The available experimental data suggest that amphibole would crystallize early and yield SiO₂-enriched liquids at depths greater than 4.5 km for P_H2O's in the range 0.6–1.0 P_total.The major problem in interpreting any of the natural plagiogranites as products of silicate liquid immiscibility is the fact that neither the Fe-enriched conjugate liquid or its crystalline equivalent has been described in the ophiolite or MOR literature. The identification of this Fe-rich conjugate magma is essential in any rock suite if a completely convincing case for silicate liquid immiscibility is to be made.     

Experimental crystallization of chrome spinel in FAMOUS basalt 527-1-1

FAMOUS basalt 527-1-1 (a high-Mg oceanic pillow basalt) has three generations of spinel which can be distinguished petrographically and chemically. The first generation (Group I) have reaction coronas and are high in Al₂O₃. The second generation (Group II) have no reaction coronas and are high in Cr₂O₃ and the third generation (Group III) are small, late-stage spinels with intermediate Al₂O₃ and Cr₂O₃. Experimental synthesis of spinels from fused rock powder of this basalt was carried out at temperatures of 1175–1270°C and oxygen fugacities of 10^?5.5 to 10^?10 atm at 1 atm pressure. Spinel is the liquidus phase at oxygen fugacities of 10^?8.5 atm and higher but it does not crystallize at any temperature at oxygen fugacities less than 10^?9.5. The composition of our spinels synthesized at 1230–1250°C and 10^?9 atmf_O2 are most similar to the high-Cr spinels (Group II) found in the rock. Spinels synthesized at 1200°C and 10^?8.5 atm_O2 are chemically similar to the Group III spinels in 527-1-1. We did not synthesize spinel at any temperature or oxygen fugacity that are similar to the high-Al (Group I) spinel found in 527-1-1. These results indicate that the high-Cr (Group II) spinel is the liquidus phase in 527-1-1 at low pressure and Group III spinel crystallize below the liquidus (～1200°C) after eruption of the basalt on the sea floor. The high-Al spinel (Group I) could have crystallized at high pressure or from a magma enriched in Al and perhaps Mg compared to 527-1-1.     

Magma chambers beneath the Klyuchevskoy volcanic group (Kamchatka)

A 3D velocity model of the Earth’s crust beneath the Klyuchevskoy volcanic group has been constructed using the seismic tomography method. Anomalies of the velocity parameters related to the zones of magma supply to active volcanoes have been distinguished. Petrological data on the composition, temperature, and pressure of generation and crystallization of parental melts of Klyuchevskoy volcano magnesian basalts have been obtained. The parental melt corresponds to picrite (MgO = 13–14 wt %) with an ultimate saturation of SiO₂ (49–50 wt %), a high H₂O content (2.2–2.9%), and incompatible elements (Sr, Rb, Ba). This melt is formed at pressures of 15–20 kbar and temperatures of 1280–1320°C. Its further crystallization proceeds in intermediate magma chambers at two discrete pressure levels (i.e., greater than 6, and 1–2 kbar). The results of the petrological studies are in good agreement with the seismotomographic model.     

An experimental facility for investigating hydromagmatic eruptions at high-pressure and high-temperature with application to the importance of magma porosity for magma-water interaction

An experimental facility has been developed to investigate magma-water interaction (MWI). The facility operates in a high-pressure and high-temperature environment, with temperatures up to 1,200°C and pressures up to 200 MPa. Cylindrical sample-holders (20 by 180 mm in size) are heated conductively to yield a three phase (melt, crystals and gas) system, and then water (or other fluid) is injected into the sample through a capillary tube (diameter 0.5 mm, length ca. 1,000 mm) under controlled conditions. Pressure, volume and temperature changes are continuously recorded during every phase of the experiments. To test this facility, MWI is studied at subliquidus temperatures (800 and 900°C) and pressure (8 MPa), using a leucite tephrite sample with two different initial grain sizes. Because of the grain-size dependence of sintering, the two starting materials produce magmas with different textures at the same temperature: porous magma for large initial grain sizes and dense magma for small initial grain sizes. In these experiments 1.5 g of water at room temperature is injected into 6.0 g of partially molten sample at velocities ranging from 1 to 3 m/s. We find that the extent of fragmentation and transport caused by MWI are mainly controlled by the texture of the interacting sample with explosive interaction occurring only for porous magmas.     

Experimental studies of melt-peridotite reactions at 1–2 GPa and 1250–1400°C and their implications for transforming the nature of lithospheric mantle and for high-Mg signatures in adakitic rocks

Experiments of the melt-peridotite reaction at pressures of 1 and 2 GPa and temperatures of 1250–1400°C have been carried out to understand the nature of the peridotite xenoliths in the Mesozoic high-Mg diorites and basalts of the North China Craton,and further to elucidate the processes in which the Mesozoic lithospheric mantle in this region was transformed.We used Fuxin alkali basalt,Feixian alkali basalt,and Xu-Huai hornblende-garnet pyroxenite as starting materials for the reacting melts,and lherzolite xenoliths and synthesized harzburgite as starting materials for the lithospheric mantle.The experimental results indicate that:(1)the reactions between basaltic melts and lherzolite and harzburgite at 1–2 GPa and 1300–1400°C tended to dissolve pyroxene and precipitate low-Mg#olivine(Mg#=83.6–89.3),forming sequences of dunite-lherzolite(D-L)and duniteharzburgite(D-H),respectively;(2)reactions between hornblende-garnet pyroxenite and lherzolite at 1 GPa and 1250°C formed a D-H sequence,whereas reactions at 2 GPa and 1350°C formed orthopyroxenite layers and lherzolite;and(3)the reaction between a partial melt of hornblende-garnet pyroxenite and harzburgite resulted in a layer of orthopyroxenite at the boundary of the pyroxenite and harzburgite.The reacted melts have higher MgO abundances than the starting melts,demonstrating that the melt-peridotite reactions are responsible for the high-Mg#signatures of andesites or adakitic rocks.Our experimental results support the proposition that the abundant peridotite and pyroxenite xenoliths in western Shandong and the southern Taihang Mountains might have experienced multiple modifications in reaction to a variety of melts.We suggest that melt-peridotite reactions played important roles in transforming the nature of the Mesozoic lithospheric mantle in the region of the North China Craton.     

Simultaneous crystallization and melting at both the roof and floor of crustal magma chambers: Experimental study using NH4Cl–H2O binary eutectic system

Thermal and compositional evolution of magmas after emplacement of basalt into continental crust has been investigated by means of fluid dynamic experiments using a cold solid mixture with eutectic composition and a hot liquid with higher salinity in the NH₄Cl–H₂O binary eutectic system. The experiments were designed to simulate cases where crystallization of a basalt magma is accompanied by melting at both the roof and floor of a crustal magma chamber. The results show that thermal and compositional convection occur simultaneously in the solution; the thermal convection is driven by cooling at the roof and the compositional convection is driven by melting and crystallization at the floor. The roof was rapidly melted by the convective heat flux, which resulted in formation of a separate eutectic melt layer (the upper liquid layer) with negligible mixing of the underlying liquid (the lower liquid layer). On the other hand, a mushy layer formed at the floor. The compositional convection at the floor carried a low heat flux, so that the heat transfer at the floor was basically explained by simple heat conduction. The thermal boundary layer in the lower liquid layer at the interface with the upper liquid layer became thicker with time and subsequently temperature decreased upward throughout the lower liquid layer. Compositional gradient with NH₄Cl content decreasing upward formed by compositional convection in the lower liquid layer. The formation of these gradients resulted in formation of double-diffusive convecting layers in the lower liquid layer. The upward heat transfer was suppressed when compared with the case where the liquid region is homogenized by vigorous convection.These experimental results imply that, when a basalt magma is emplaced in continental crust, floor melting does not always enhance the cooling of the magma, but it may even reduce the total heat loss from the magma to the crusts due to suppression of convection by formation of a stabilizing compositional gradient.     

The mineral chemistry of pyroxenite xenoliths in the volcanic rocks of Hoh Xil and their significance

The pyroxenite xenoliths in the volcanic rocks of Hoh Xil consist of clinopyroxenes and orthopyroxenes. The mineral composition of these pyroxenes is similar to that of mantle xenoliths including peridotite and pyroxenite from China and abroad, and different from that of granulites. The pyroxenes formed at 1101–1400°C (averaging 1250°C) and under 30–60 kb (averaging 46 kb). We deduced that the magma was derived from the mantle at a depth of more than 150 km, which fits in with the geophysical conclusion that the low-velocity layer existed in the mantle under 150 km.

     

Apatite and phosphorus in mantle source regions: An experimental study of apatite/melt equilibria at pressures to 25 kbar

The solubility of fluorapatite in a wide variety of basic magmatic liquids was experimentally determined over a range of upper mantle P-T conditions (8–25 kbar, 1275–1350°C). Fluorapatite is stable over the entire range of conditions investigated, but its solubility in melts is variable, depending negatively on SiO₂ content of the melt and positively upon temperature, with relatively little sensitivity to pressure above 8 kbar. At upper mantle pressures and a temperature of 1250°C, molten basalt (50% SiO₂) will dissolve 3–4 wt.% P₂O₅ before saturation in apatite is reached. For a magma 100°C cooler or containing 10 wt.% more SiO₂, apatite saturation occurs at less than 2 wt.% dissolved P₂O₅. The observed high solubility of apatite in basic magmas at their normal near-liquidus temperatures virtually precludes the occurrence of residual apatite in mantle source regions. If relatively low-temperature melting conditions prevail (e.g., 1100°C), as might be possible in H₂O-bearing regions of the upper mantle, apatite could remain in the residue, but only in amounts too small to have significant effects on the rare earth patterns of the liquids.Because of the high solubility of apatite in basic magmas, phosphorus can be confidently treated as an incompatible element in peridotite melting models. Such models, in combination with observed characteristics of basic lavas, indicate that the upper mantle contains ～200 ppm of phosphorus, much less than the chondritic abundance of ～900 ppm.     

The petrology and geochemistry of the Handkerchief Mesa mixed magma complex, San Juan Mountains, Colorado

The Handkerchief Mesa mixed magma complex is one of several late Cenozoic volcanic complexes in the southeastern San Juan Mountains characterized by mingling and limited mixing of basalt and rhyodacite. Stratigraphy in the dissected vent complex at Handkerchief Mesa records three phases of volcanism, the first and third displaying evidence for coeruption of mafic and silicic magmas. Phases 1 and 2 erupted silicic pyroclastics and basaltic lava flows, respectively. Phase-3 eruptions were dominated by rhyodacite lava flows, rhyodacite dikes, and abundant mingled and mixed hybrid lavas.Pre- and syneruptive basalt-rhyodacite mixing of phase-3 eruptions is shown by: (1) inclusions of quenched basalt in rhyodacite; (2) partially disaggregated basalt inclusions in mixed hybrids and rhyodacites; (3) interfingering lenses of mixed hybrid lavas and rhyodacite. Whole-rock major- and trace-element analyses support a two-component mixing model whereby intermediate hybrids are produced by mixing of basalt and rhyodacite (up to 30% basalt: 70% rhyodacite). Disequilibrium phenocryst textures and mineral compositions are consistent with multistage mixing culminating in an eruptive mixing event. Protracted mixing along a boundary zone at the base of a rhyodacite magma chamber may be responsible for stabilizing Fe-rich olivine phenocrysts in some hybrids.Basalt-rhyodacite mixing is inhibited by rapid crystallization in the basalt shortly after inclusion within the lower temperature melt. The degree to which mechanical dispersion and blending ensues is a critical function of the initial temperature contrast (ΔT_i) between the two magmas. Thermal models, simulating the conductive cooling histories for basalt spheres in rhyodacite reservoirs, suggest that at large ΔT_i's (> 200°) rapid cooling of the inclusion leads to disequilibrium crystallization with concomitant depression of equilibrium solidi, grain boundary wetting by residual liquids, and limited disaggregation of the inclusion imposed by movement of the host. For small ΔT_i's (< 100°) temperatures within the inclusion can be maintained above the solidus for prolonged time periods, enhancing the possibility of producing homogeneous mixed hybrids through mechanical blending and diffusion. Both mechanisms operated at Handkerchief Mesa and contributed to the range of observed textures and compositions.     

Petrology of clinopyroxene-amphibole inclusions from the roque nublo volcanics,gran canaria,canary islands

Inclusions consisting of clinopyroxene, amphibole, Fe-Ti oxides and apatitc are abundant in the Roque Nublo volcanics, a unit of Late Tertiary age that is widespread on Gran Canaria Island. The unit includes alkalic basalts and breccias. Mafic minerals in several inclusions and in one basalt host have been analysed with the electron microprobe. Although the inclusions vary in size, texture and mineralogy, they show certain common teatures. The pyroxenes analyzed are all salites-augites and their position in the Ca-Fe Mg quadrilateral suggests that they are early formed representatives of the pyroxene crystallization trend characteristic of alkaliolivine basalt. The amphibole is invariably kaersutite. A common variety of inclusion is composed largely of kaersutite and titaniferous clinopyroxene. The kaersutite (TiO₂ 5.27%, K₂O 1.58%) is homogeneous, except for slight iron enrichment in the margins of crystals. The clinopyroxene is an hourglass-zoned, brownish titansalite, Ca 50 Mg 35 Fe 15, TiO₂ 3.08%, with a green core of Ca 49 Mg 38 Fe 13, TiO₂ 2.15%. Compositions of coexisting titanilerous magnetite and ilmenite, Usp 44 Mt 56 and Ilm 85 Hem 15, respectively, indicate they formed at approximately 975°C and pO, 10^?10.5 atm. In another type of inclusion and its host basalt, pyroxene relations are more complex. Inclusion pyroxene is markedly but diffusely zoned. Predominant is a green salite, Ca 47 Mg 38 Fe 15, TiO₂ 1.11%, which has small, patchy core zones of brownish. Ti-rich salite. Ca 48 Mg 35 Fe 17, TiO₂ 1.94%. Cores of crystals in the host basalt are Ca 47 Mg 41 Fe 12, TiO₂ 2.23%; rims are pale green, Cr-rich diopsidic augite, Ca 44 Mg 45 Fe 11, TiO₂ 1.32%, Cr₂O₃ 0.48%. This «reverse» Fe-Mg zoning is attributed to increasing partial pressure of oxygen as crystallization proceeded. Kaersutite similar to that mentioned above occurs in both the inclusion and its host, in which it is highly resorbed. The available field and analytical evidence strongly suggests that the inclusions and the associated basalts are genetically related. Resorption of the kaersutite at depth may have given rise to the alkalic basalts of the Roque Nublo series.