The basal ash deposit of the Sovana Eruption (Vulsini Volcanoes, central Italy): the product of a dilute pyroclastic density current

A low aspect ratio, decimeter-thick ash deposit, axisymmetrically distributed around the Latera Caldera (Western Vulsini Volcanoes, central Italy) has been studied by means of field and laboratory investigations. Field studies comprise facies analysis at centimeter scale and maximum clast size and deposit thickness measurements. Grain size and component distribution, chemical composition and particle morphoscopic features have been determined on selected samples. We discuss the co-ignimbrite ash fall vs. pyroclastic surge origin of the deposit and the hydrovolcanic vs. magmatic eruption nature. Complex facies association, textural features and grain size data rule out an ash fall origin for the whole deposit. The hydrovolcanic nature of the eruption has been discarded on the grounds of componentry and morphoscopic features of vitric fragments. We propose that the main body of the ash deposit formed from a radially expanding, dilute, turbulent pyroclastic density current, originated by a continuous collapse of a low-altitude (a few kilometers) eruptive column with a possible radial jet component.     

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.     

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

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

A model that helps explain Sr-isotope disequilibrium between feldspar phenocrysts and melt in large-volume silicic magma systems

Feldspar phenocrysts of silicic volcanic rocks are commonly in Sr-isotopic disequilibrium with groundmass. In some cases the feldspar is more radiogenic, and in others it is less radiogenic. Several explanations have been published previously, but none of these is able to accommodate both senses of disequilibrium. We present a model by which either more- or less-radiogenic feldspar (or even both within a single eruptive unit) can originate. The model requires a magma body open to interaction with biotite- and feldspar-bearing wall rock. Magma is incrementally contaminated as wall rock melts incongruently. Biotite preferentially melts first, followed by feldspar. Such melting behavior, which is supported by both field and experimental studies, first contaminates magma with a relatively radiogenic addition, followed by a less-radiogenic addition. Feldspar phenocrysts lag behind melt (groundmass of volcanic rock) in incorporating the influx of contaminant, thus resulting in Sr-isotopic disequilibrium between the crystals and melt. The sense of disequilibrium recorded in a volcanic rock depends on when eruption quenches the contamination process. This model is testable by isotopic fingerprinting of individual feldspar crystals. For a given set of geologic boundary conditions, specific core-to-rim Sr-isotopic profiles are expectable. Moreover, phenocrysts that nucleate at different times during the contamination process should record different and predictable parts of the history. Initial results of Sr-isotopic fingerprinting of sanidine phenocrysts from the Taylor Creek Rhyolite are consistent with the model. More tests of the model are desirable.     

Debris-avalanche deposits of the Milo Lahar sequence and the opening of the Valle del Bove on Etna volcano (Italy)

Previously undescribed debris-avalanche deposits occur in two locations downslope from the open end of the Valle del Bove. These outcrops comprise unstratified, ungraded deposits of metre-scale lava blocks in a matrix of weathered and fractured lava clasts. The avalanche deposits are unconformably overlain by matrix- to clast-supported conglomerates, representing debris-flow and interbedded fluvial deposits, that constitute most of the Milo Lahar sequence. We present evidence that the Milo Lahar sequence, which crops out just at the exit of the Valle del Bove, formed during the opening and enlargement of this depression. The presence of the avalanche deposits at the base of the Milo Lahar sequence indicates that catastrophic landslides were involved in the formation of the Valle del Bove. The composition of lavas in the debris avalanche deposits is similar to that of most of the Ellittico volcanic sequence exposed along the northern wall of the Valle del Bove. Radiocarbon dates of 8400 and 5300 years BP from the base and top, respectively, of the debris-flow sequence indicate that the Milo Lahars are correlative with the exposed part of the Chiancone deposit. The basal lahars of the Chiancone, which contain lava blocks whose compositions partially overlap that of blocks in the avalanche deposits, may have formed by water concentration in the distal end of the avalanche causing transformation to debris, or alternatively by reworking of the avalanche deposit.     

Generation of pyroclastic flows and surges by hot-rock avalanches from the dome of Mount St. Helens volcano,USA

Several hot-rock avalanches have occurred during the growth of the composite dome of Mount St. Helens, Washington between 1980 and 1987. One of these occurred on 9 May 1986 and produced a fan-shaped avalanche deposit of juvenile dacite debris together with a more extensive pyroclastic-flow deposit. Laterally thinning deposits and abrasion and baking of wooden and plastic objects show that a hot ash-cloud surge swept beyond the limits of the pyroclastic flow. Plumes that rose 2–3 km above the dome and vitric ash that fell downwind of the volcano were also effects of this event, but no explosion occurred. All the facies observed originated from a single avalanche. Erosion and melting of craterfloor snow by the hot debris caused debris flows in the crater, and a small flood that carried juvenile and other clasts north of the crater. A second, broadly similar event occured in October 1986. Larger events of this nature could present a significant volcanic hazard.     

Contributions of slab fluid and sediment melt components to magmatism in the Mariana Arc–Trough system: Evidence from geochemical compositions and Sr,Nd, and noble gas isotope systematics

This study presents new major and trace element, mineral, and Sr, Nd, and noble gas isotope geochemical analyses of basalts, gabbro, and clinopyroxenite from the Mariana Arc (Central Islands and Southern Seamount provinces) including the forearc, and the Mariana Trough (Central Graben and Spreading Ridge). Mantle source compositions beneath the Mariana Arc and the Mariana Trough indicate a mantle source that is depleted in high field strength elements relative to MORB (mid‐oceanic ridge basalt). Samples from the Mariana Arc, characterized by high ratios of Ba/Th, U/Th, ⁸⁴Kr/⁴He and ¹³²Xe/⁴He, are explained by addition of fluid from the subducted slab to the mantle wedge. Correlations of noble gas data, as well as large ion lithophile elements, indicate that heavy noble gases (Ar, Kr, and Xe) provide evidence for fluid fluxing into the mantle wedge. On the other hand, major elements and Sr, Nd, He, and Ne isotopic data of basalts from the Mariana Trough are geochemically indistinguishable from MORB. Correlations of ³He/⁴He and ⁴⁰Ar/³⁶Ar in the Mariana Trough samples are explained by mixing between MORB and atmosphere. One sample from the Central Graben indicates extreme enrichment in ²⁰Ne/²²Ne and ²¹Ne/²²Ne, suggesting incorporation of solar‐type Ne in the magma source. Excess ¹²⁹Xe is also observed in this sample suggesting primordial noble gases in the mantle source. The Mariana Trough basalts indicate that both fluid and sediment components contributed to the basalts, with slab‐derived fluids dominating beneath the Spreading Ridge, and that sediment melts, characterized by high La/Sm and relatively low U/Th and Zr/Nb, dominate in the source region of basalts from the Central Graben.