Ar/Ar age and geochemistry of the post-collisional Miocene Yamadağ volcanics in the Arapkir area (Malatya Province), eastern Anatolia, Turkey

The Neogene Yamadağ volcanics occupy a vast area between Sivas and Malatya in eastern Anatolia, Turkey. These volcanic rocks are characterized by pyroclastics comprising agglomerates, tuffs and some small outcrops of basaltic–andesitic–dacitic rocks, overlain upward by basaltic and dacitic rocks, and finally by basaltic lava flows in the Arapkir area, northern Malatya Province. The basaltic lava flows in the Arapkir area yield a ⁴⁰Ar/³⁹Ar age of 15.8 ± 0.2 Ma, whereas the dacitic lava flows give ⁴⁰Ar/³⁹Ar ages ranging from 17.6 through 14.7 ± 0.1 to 12.2 ± 0.2 Ma, corresponding to the Middle Miocene. These volcanic rocks have subalkaline basaltic, basaltic andesitic; alkaline basaltic trachyandesitic and dacitic chemical compositions. Some special textures, such as spongy-cellular, sieve and embayed textures; oscillatory zoning and glass inclusions in plagioclase phenocrysts; ghost amphiboles and fresh biotite flakes are attributable to disequilibrium crystallization related to magma mixing between coeval magmas. The main solidification processes consist of fractional crystallization and magma mixing which were operative during the soldification of these volcanic rocks. The dacitic rocks are enriched in LILE, LREE and Th, U type HFSE relative to the basaltic rocks. The basaltic rocks also show some marked differences in terms of trace-element and REE geochemistry; namely, the alkaline basaltic trachyandesites have pronounced higher HFSE, MREE and HREE contents relative to the subalkaline basalts. Trace and REE geochemical data reveal the existence of three distinct magma sources – one subalkaline basaltic trachyandesitic, one alkaline basaltic and one dacitic – in the genesis of the Yamadağ volcanics in the Arapkir region. The subalkaline basaltic and alkaline basaltic trachyandesitic magmas were derived from an E-MORB type enriched mantle source with a relatively high- and low-degree partial melting, respectively. The magmatic melt of dacitic rocks seem to be derived from an OIB-type enriched lithospheric mantle with a low proportion of partial melting. The enriched lithospheric mantle source reflect the metasomatism induced by earlier subduction-derived fluids. All these coeval magmas were generated in a post-collisional extensional geodynamic setting in Eastern Anatolia, Turkey.     

Early Cretaceous trachybasalt-trachyte-trachyrhyolitic volcanism in the Nyalga basin (Central Mongolia): sources and evolution of continental rift magmas

As shown by geological, mineralogical, and isotope geochemical data, trachybasaltic-trachytic-trachyrhyolitic (TTT) rocks from the Nyalga basin in Central Mongolia result from several eruptions of fractionated magmas within a short time span at about 120 Ma. Their parental basaltic melts formed by partial melting of mantle peridotite which was metasomatized and hydrated during previous subduction events. Basaltic trachyandesites have high TiO₂ and K₂O, relatively high P₂O₅, and low MgO contents, medium ⁸⁷Sr/⁸⁶Sr(₀) ratios (0.70526-0.70567), and almost zero or slightly negative ε_Nd(T) values. The isotope geochemical signatures of TTT rocks are typical of Late Mesozoic basaltic rocks from rift zones of Mongolia and Transbaikalia. The sources of basaltic magma at volcanic centers of Northern and Central Asia apparently moved from a shallower and more hydrous region to deeper and less hydrated lithospheric mantle (from spinel to garnet-bearing peridotite) between the Late Paleozoic and the latest Mesozoic. The geochemistry and mineralogy of TTT rocks fit the best models implying fractional crystallization of basaltic trachyandesitic, trachytic, and trachyrhyodacitic magmas. Mass balance calculations indicate that trachytic and trachydacitic magmas formed after crystallization of labradorite-andesine, Ti-augite, Sr-apatite, Ti-magnetite, and ilmenite from basaltic trachyandesitic melts. The melts evolved from trachytic to trachyrhyodacitic and trachyrhyolitic compositions as a result of prevalent crystallization of K-Na feldspar, with zircon, chevkinite-Ce, and LREE-enriched apatite involved in fractionation. Trachytic, trachyrhyodacitic, and trachyrhyolitic residual melts were produced by the evolution of compositionally different parental melts (basaltic trachyandesitic, trachytic, and trachyrhyodacitic, respectively), which moved to shallower continental crust and accumulated in isolated chambers. Judging by their isotopic signatures, the melts assimilated some crustal material, according to the assimilation and fractional crystallization (AFC) model.     

Storage conditions of Bezymianny Volcano parental magmas: results of phase equilibria experiments at 100 and 700 MPa

The crystallization sequence of a basaltic andesite from Bezymianny Volcano, Kamchatka, Russia, was simulated experimentally at 100 and 700 MPa at various water activities (aH₂O) to investigate the compositional evolution of residual liquids. The temperature (T) range of the experiments was 950–1,150 °C, aH₂O varied between 0.1 and 1, and the log of oxygen fugacity (fO₂) varied between quartz–fayalite–magnetite (QFM) and QFM + 4.1. The comparison of the experimentally produced liquids and natural samples was used to constrain the pressure (P)–T–aH₂O–fO₂ conditions of the Bezymianny parental magma in the intra-crustal magma plumbing system. The phase equilibria constraints suggest that parental basaltic andesite magmas should contain ~2–2.5 wt% H₂O; they can be stored in upper crustal levels at a depth of ~15 km, and at this depth they start to crystallize at ~1,110 °C. The subsequent chemical evolution of this parental magma most probably proceeded as decompressional crystallization occurred during magma ascent. The final depths at which crystallization products accumulated prior to eruption are not well constrained experimentally but should not be shallower than 3–4 km because amphibole is present in natural magmas (>150 MPa). Thus, the major volume of Bezymianny andesites was produced in a mid-crustal magma chamber as a result of decompressional crystallization of parental basaltic andesites, accompanied by mixing with silicic products from the earlier stages of magma fractionation. In addition, these processes are complicated by the release of volatiles due to magma degassing, which occurs at various stages during magma ascent.     

Magnesian andesite and dacite lavas from Mt. Shasta,northern California: products of fractional crystallization of H<Subscript>2</Subscript>O-rich mantle melts

Mt. Shasta andesite and dacite lavas contain high MgO (3.5–5 wt.%), very low FeO*/MgO (1–1.5) and 60–66 wt.% SiO₂. The range of major and trace element compositions of the Shasta lavas can be explained through fractional crystallization (~50–60 wt.%) with subsequent magma mixing of a parent magma that had the major element composition of an H₂O-rich primitive magnesian andesite (PMA). Isotopic and trace element characteristics of the Mt. Shasta stratocone lavas are highly variable and span the same range of compositions that is found in the parental basaltic andesite and PMA lavas. This variability is inherited from compositional variations in the input contributed from melting of mantle wedge peridotite that was fluxed by a slab-derived, fluid-rich component. Evidence preserved in phenocryst assemblages indicates mixing of magmas that experienced variable amounts of fractional crystallization over a range of crustal depths from ~25 to ~4 km beneath Mt. Shasta. Major and trace element evidence is also consistent with magma mixing. Pre-eruptive crystallization extended from shallow crustal levels under degassed conditions (~4 wt.% H₂O) to lower crustal depths with magmatic H₂O contents of ~10–15 wt.%. Oxygen fugacity varied over 2 log units from one above to one below the Nickel-Nickel Oxide buffer. The input of buoyant H₂O-rich magmas containing 10–15 wt.% H₂O may have triggered magma mixing and facilitated eruption. Alternatively, vesiculation of oversaturated H₂O-rich melts could also play an important role in mixing and eruption.     

Sulphur solubility in andesitic to basaltic melts: implications for Hekla volcano

The solubility of sulphur in sulphide-saturated, H₂O-bearing basaltic–andesitic and basaltic melts from Hekla volcano (Iceland) has been determined experimentally at 1,050°C, 300 and 200 MPa, and redox conditions with oxygen fugacity (logfO₂) between QFM−1.2 and QFM+1.1 (QFM is a quartz–fayalite–magnetite oxygen buffer) in the systems containing various amounts of S and H₂O. The S content of the H₂O-rich glasses saturated with pyrrhotite decreases from 2,500 ppm in basalt to 1,500 ppm in basaltic andesite at the investigated conditions. Furthermore, the reduction of water content in the melt at pyrrhotite saturation and fixed T, P and redox conditions leads to a decrease in S concentration from 2,500 to 1,400 ppm for basaltic experiments (for H₂O decrease from 7.8 to 1.4 wt%) and from 1,500 to 900 ppm (for H₂O decrease from 6.7 to 1.7 wt%) for basaltic andesitic experiments. Our experimental data, combined with silicate melt inclusion investigations and the available models on sulphide saturation in mafic magmas, indicate that the parental basaltic melts of Hekla were not saturated with respect to sulphide. During magmatic differentiation, the S content in the residual melts increased and might have reached sulphide saturation with 2,500 ppm dissolved S. With further magma crystallization, the S concentration in the melt was controlled by the sulphide saturation of the magma, decreasing from ~2,500 to 900 ppm S.     

Amphibole as an archivist of magmatic crystallization conditions: problems,potential, and implications for inferring magma storage prior to the paroxysmal 2010 eruption of Mount Merapi,Indonesia

Amphibole is widely employed to calculate crystallization temperature and pressure, although its potential as a geobarometer has always been debated. Recently, Ridolfi et al. (Contrib Mineral Petrol 160:45–66, 2010) and Ridolfi and Renzulli (Contrib Mineral Petrol 163:877–895, 2012) have presented calibrations for calculating temperature, pressure, fO₂, melt H₂O, and melt major and minor oxide composition from amphibole with a large compositional range. Using their calibrations, we have (i) calculated crystallization conditions for amphibole from eleven published experimental studies to examine the problems and the potential of the new calibrations; and (ii) calculated crystallization conditions for amphibole from basaltic–andesitic pyroclasts erupted during the paroxysmal 2010 eruption of Mount Merapi in Java, Indonesia, to infer pre-eruptive conditions. Our comparison of experimental and calculated values shows that calculated crystallization temperatures are reasonable estimates. Calculated fO₂ and melt SiO₂ content yields potentially useful estimates at moderately reduced to moderately oxidized conditions and intermediate to felsic melt compositions. However, calculated crystallization pressure and melt H₂O content are untenable estimates that largely reflect compositional variation in the crystallizing magmas and crystallization temperature and not the calculated parameters. Amphibole from Merapi’s pyroclasts yields calculated conditions of ~200–800 MPa, ~900–1,050 °C, ~NNO + 0.3–NNO + 1.1, ~3.7–7.2 wt% melt H₂O, and ~58–71 wt% melt SiO₂. We interpret the variations in calculated temperature, fO₂, and melt SiO₂ content as reasonable estimates, but conclude that the large calculated pressure variation for amphibole from Merapi and many other arc volcanoes is evidence for thorough mixing of mafic to felsic magmas and not necessarily evidence for crystallization over a large depth range. In contrast, bimodal pressure estimates obtained for other arc magmas reflect amphibole crystallization from mafic and more evolved magmas, respectively, and should not necessarily be taken as evidence for crystallization in two reservoirs at variable depth.     

Magmatic processes that generated the rhyolite of Glass Mountain, Medicine Lake volcano, N. California

Glass Mountain consists of a 1 km³, compositionally zoned rhyolite to dacite glass flow containing magmatic inclusions and xenoliths of underlying shallow crust. Mixing of magmas produced by fractional crystallization of andesite and crustal melting generated the rhyolite of Glass Mountain. Melting experiments were carried out on basaltic andesite and andesite magmatic inclusions at 100, 150 and 200 MPa, H₂O-saturated with oxygen fugacity controlled at the nickel-nickel oxide buffer to provide evidence of the role of fractional crystallization in the origin of the rhyolite of Glass Mountain. Isotopic evidence indicates that the crustal component assimilated at Glass Mountain constitutes at least 55 to 60% of the mass of erupted rhyolite. A large volume of mafic andesite (2 to 2.5 km³) periodically replenished the magma reservoir(s) beneath Glass Mountain, underwent extensive fractional crystallization and provided the heat necessary to melt the crust. The crystalline residues of fractionation as well as residual liquids expelled from the cumulate residues are preserved as magmatic inclusions and indicate that this fractionation process occurred at two distinct depths. The presence and composition of amphibole in magmatic inclusions preserve evidence for crystallization of the andesite at pressures of at least 200 MPa (6 km depth) under near H₂O-saturated conditions. Mineralogical evidence preserved in olivine-plagioclase and olivine-plagioclase-high-Ca clinopyroxene-bearing magmatic inclusions indicates that crystallization under near H₂O-saturated conditions also occurred at pressures of 100 MPa (3 km depth) or less. Petrologic, isotopic and geochemical evidence indicate that the andesite underwent fractional crystallization to form the differentiated melts but had no chemical interaction with the melted crustal component. Heat released by the fractionation process was responsible for heating and melting the crust. Received: 26 March 1996 / Accepted: 14 November 1996     

Fluid history of UHP metamorphism in Dabie Shan, China: a fluid inclusion and oxygen isotope study on the coesite-bearing eclogite from Bixiling

This paper characterizes late Holocene basalts and basaltic andesites at Medicine Lake volcano that contain high pre-eruptive H₂O contents inherited from a subduction related hydrous component in the mantle. The basaltic andesite of Paint Pot Crater and the compositionally zoned basaltic to andesitic lavas of the Callahan flow erupted approximately 1000 ¹⁴C years Before Present (¹⁴C years b.p.). Petrologic, geochemical and isotopic evidence indicates that this late Holocene mafic magmatism was characterized by H₂O contents of 3 to 6 wt% H₂O and elevated abundances of large ion lithophile elements (LILE). These hydrous mafic inputs contrast with the preceding episodes of mafic magmatism (from 10,600 to ∼3000 ¹⁴C years b.p.) that was characterized by the eruption of primitive high alumina olivine tholeiite (HAOT) with low H₂O (<0.2 wt%), lower LILE abundance and different isotopic characteristics. Thus, the mantle-derived inputs into the Medicine Lake system have not always been low H₂O, primitive HAOT, but have alternated between HAOT and hydrous subduction related, calc-alkaline basalt. This influx of hydrous mafic magma coincides temporally and spatially with rhyolite eruption at Glass Mountain and Little Glass Mountain. The rhyolites contain quenched magmatic inclusions similar in character to the mafic lavas at Callahan and Paint Pot Crater. The influence of H₂O on fractional crystallization of hydrous mafic magma and melting of pre-existing granite crust beneath the volcano combined to produce the rhyolite. Fractionation under hydrous conditions at upper crustal pressures leads to the early crystallization of Fe-Mg silicates and the suppression of plagioclase as an early crystallizing phase. In addition, H₂O lowers the saturation temperature of Fe and Mg silicates, and brings the temperature of oxide crystallization closer to the liquidus. These combined effects generate SiO₂-enrichment that leads to rhyodacitic differentiated lavas. In contrast, low H₂O HAOT magmas at Medicine Lake differentiate to iron-rich basaltic liquids. When these Fe-enriched basalts mix with melted granitic crust, the result is an andesitic magma. Since mid-Holocene time, mafic volcanism has been dominated primarily by hydrous basaltic andesite and andesite at Medicine Lake Volcano. However, during the late Holocene, H₂O-poor mafic magmas continued to be erupted along with hydrous mafic magmas, although in significantly smaller volumes. Received: 4 January 1999 / Accepted: 30 August 1999     

Contrasting compositional trends of rocks and olivine-hosted melt inclusions from Cerro Negro volcano (Central America): implications for decompression-driven fractionation of hydrous magmas

Melt inclusions in olivine Fo_83–72 from tephras of 1867, 1971 and 1992 eruptions of Cerro Negro volcano represent a series of basaltic to andesitic melts of narrow range of MgO (5.6–8 wt %) formed by ~46 wt % fractional crystallization of olivine (~6 wt %), plagioclase (~27 wt %), pyroxene (~13 wt %) and magnetite (<1 wt %) from primitive basaltic melt (average SiO₂ = 49 wt %, MgO = 7.6 wt %, H₂O = 6 wt %) as it ascended to the surface from the depth of about 14 km. The crystallization occurred at increasing liquidus temperature from 1,050 to 1,090 °C in the pressure range from 400 to 50 MPa and was induced by release of mixed H₂O–CO₂ fluid from the melt at decreasing pressure. Matrix glass compositions fall at the high-Si end of the melt inclusion trend and represent the final stage of melt crystallization during and after eruption. The bulk compositions of erupted Cerro Negro magmas (tephras and lavas) range from high- to low-MgO (3–10 wt %) basalts, which form a compositional array crossing the trend of melt inclusions so that virtually no rock from Cerro Negro has composition akin to true melt represented by the inclusions. The variations of the bulk magma (rocks) and melt (melt inclusions) compositions can be generated in a dyke connecting a deep primitive magma reservoir with the Cerro Negro edifice. While the melt inclusions represent the compositional trend of instantaneous melts along the magma pathway at decreasing pressure and H₂O content, occurrence of low-Mg to high-Mg basalts reflects the process of phenocryst re-distribution in progressively evolving melt. The crystallization scenario is anticipated to operate everywhere in dykes feeding basaltic volcanoes and can explain the predominance of plagioclase-rich high-Al basalts in island arc as well as typical compositional variations of magmas during single eruptions.     

Relative contributions of crust and mantle to generation of Campanian high-K calc-alkaline I-type granitoids in a subduction setting, with special reference to the Harşit Pluton, Eastern Turkey

We present elemental and Sr–Nd–Pb isotopic data for the magmatic suite (~79 Ma) of the Harşit pluton, from the Eastern Pontides (NE Turkey), with the aim of determining its magma source and geodynamic evolution. The pluton comprises granite, granodiorite, tonalite and minor diorite (SiO₂ = 59.43–76.95 wt%), with only minor gabbroic diorite mafic microgranular enclaves in composition (SiO₂ = 54.95–56.32 wt%), and exhibits low Mg# (<46). All samples show a high-K calc-alkaline differentiation trend and I-type features. The chondrite-normalized REE patterns are fractionated [(La/Yb) _n  = 2.40–12.44] and display weak Eu anomalies (Eu/Eu* = 0.30–0.76). The rocks are characterized by enrichment of LILE and depletion of HFSE. The Harşit host rocks have weak concave-upward REE patterns, suggesting that amphibole and garnet played a significant role in their generation during magma segregation. The host rocks and their enclaves are isotopically indistinguishable. Sr–Nd isotopic data for all of the samples display I _Sr = 0.70676–0.70708, ε _Nd(79 Ma) = −4.4 to −3.3, with T _DM = 1.09–1.36 Ga. The lead isotopic ratios are (²⁰⁶Pb/²⁰⁴Pb) = 18.79–18.87, (²⁰⁷Pb/²⁰⁴Pb) = 15.59–15.61 and (²⁰⁸Pb/²⁰⁴Pb) = 38.71–38.83. These geochemical data rule out pure crustal-derived magma genesis in a post-collision extensional stage and suggest mixed-origin magma generation in a subduction setting. The melting that generated these high-K granitoidic rocks may have resulted from the upper Cretaceous subduction of the Izmir–Ankara–Erzincan oceanic slab beneath the Eurasian block in the region. The back-arc extensional events would have caused melting of the enriched subcontinental lithospheric mantle and formed mafic magma. The underplating of the lower crust by mafic magmas would have played a significant role in the generation of high-K magma. Thus, a thermal anomaly induced by underplated basic magma into a hot crust would have caused partial melting in the lower part of the crust. In this scenario, the lithospheric mantle-derived basaltic melt first mixed with granitic magma of crustal origin at depth. Then, the melts, which subsequently underwent a fractional crystallization and crustal assimilation processes, could ascend to shallower crustal levels to generate a variety of rock types ranging from diorite to granite. Sr–Nd isotope modeling shows that the generation of these magmas involved ~65–75% of the lower crustal-derived melt and ~25–35% of subcontinental lithospheric mantle. Further, geochemical data and the Ar–Ar plateau age on hornblende, combined with regional studies, imply that the Harşit pluton formed in a subduction setting and that the back-arc extensional period started by least ~79 Ma in the Eastern Pontides.     

Processes of the formation of mugearitic and benmoreitic magmas on Nemrut Volcano (East Turkey)

The samples of trachybasalt, mugearite, benmoreite, trachydacite, and comendite from Nemrut Volcano (East Turkey) were studied. Except for trachybasalt, each sample contains partly dissolved mineral xenocrysts from magmas with different compositions. At the precaldera stage of volcanic evolution fractional crystallization of the alkali basaltic melt contaminated with a small amount of material of the upper crust, as well as mixing of trachybasaltic and trachydacitic magmas, could result in the formation of mugearitic magma. At the precaldera stage benmoreitic magma formed as a result of the evolution of trachybasaltic and mugearitic magmas, while at the postcaldera stage—after the mixing of trachybasaltic magma and low-Fe comenditic melt. The presence of relics of postcaldera benmoreitic magma in comendite (glass of trachyrhyodacite–trachyrhyolite composition, xenocrysts of Mg-rich olivine, plagioclase, and augite) allows us to assume that repeated eruptions at the postcaldera stage of volcanic evolution were caused by its eruptions into the low-Fe comenditic magma.     

Crystal Clusters, Feldspar Glomerocrysts, and Magma Envelopes in the Atascosa Lookout Lava Flow, Southern Arizona, USA: Recorders of Magmatic Events

The Atascosa Lookout trachyandesite lava flow is the youngestand most compositionally primitive unit in the middle TertiaryAtascosa–Tumacacori–Cerro Colorado volcanic complex(ATCC). The flow hosts a variety of objects of contrasting origin,including (1) clusters of plagioclase ± chromian diopside,magnesian augite, quartz, hornblende, and orthopyroxene; (2)amoeboid-shaped quartz-bearing enclaves; (3) plagioclase crystalswith a concentric interior zone of small melt inclusions (dustyplagioclase); (4) plagioclase crystals with cores filled withlarge melt inclusions (honeycomb plagioclase); (5) plagioclaseglomerocrysts. The groundmass of the trachyandesitic flow istrachydacite. Some crystal clusters, enclaves, and plagioclaseglomerocrysts are surrounded by diffuse envelopes of trachydacitehigher in K and Mg and lower in Si than the trachydacitic groundmassof the flow. This envelope material is interpreted as foreignmagma that engulfed these objects as it invaded their host magma.Both the crystal clusters and plagioclase glomerocrysts maybe the remains of cumulate crystal layers, disrupted by influxesof magma into their reservoirs. Crystals in the lava flow originatedin at least three distinct magmas and their hybrids. The groundmassof the lava flow preserves evidence for repeated infusion ofenvelope magma into the system. These influxes fueled the invasionof crystal clusters, plagioclase glomerocrysts, enclaves, andswirls of the envelope magma into the groundmass of the AtascosaLookout lava flow. Despite the compositional and textural varietyapparent in the lava flow, the magmas involved in its developmentmay have been genetically closely related. The collection offeatures in the lava flow resulted from the development of compositionallayers in the magma, accumulation of crystal-rich horizons,disturbance of the system by repeated magma influx, and minorcrustal assimilation. KEY WORDS: crystal clusters; enclaves; glomerocrysts; trachyandesite     

Magma storage and ascent during the 1995 eruption of Fogo,Cape Verde Archipelago

The 1995 eruption of Fogo (Cape Verde Islands) differed from previous eruptions by the occurrence of evolved lavas, the SW-orientation of vents, and pre-eruptive seismicity between Fogo and the adjacent (~20 km) island of Brava. We have conducted a thermobarometric and chemical study of this eruption in order to reconstruct its magma plumbing system and to test for possible connections to Brava. The bimodal eruption produced basanites (5.2–6.7 wt% MgO) and phonotephrites (2.4–2.8 wt% MgO) that are related by fractional crystallization. Clinopyroxene-melt-barometry of phenocrysts yields pressure ranges of 460–680 MPa for the basanites and 460–520 MPa for the phonotephrites. Microthermometry of CO₂-dominated fluid inclusions in olivine and clinopyroxene phenocrysts yields systematically lower pressure ranges of 200–310 MPa for basanites and 270–470 MPa for phonotephrites. The combined data indicate pre-eruptive storage of the 1995 magmas within the lithospheric mantle between 16 and 24 km depth. During eruption, the ascending magmas stalled temporarily at 8–11 km depth, within the lower crust, before they ascended to the surface in a few hours as indicated by zonations of olivine phenocrysts. Our data provide no evidence for magma storage at shallow levels (<200 MPa) or lateral magma movements beneath the Fogo-Brava platform. Sr–Nd–Pb isotope ratios of samples from Brava differ significantly from those of the 1995 and older Fogo lavas, which rules out contamination of the 1995 magmas by Brava material and indicates different mantle sources and magma plumbing systems for both islands.     

Amphibole perspective to unravel pre-eruptive processes and conditions in volcanic plumbing systems beneath intermediate arc volcanoes: a case study from Ciomadul volcano (SE Carpathians)

Ciomadul is the youngest volcano in the Carpathian–Pannonian region produced crystal-rich high-K dacites that contain abundant amphibole phenocrysts. The amphiboles in the studied dacites are characterized by large variety of zoning patterns, textures, and a wide range of compositions (e.g., 6.4–15 wt% Al₂O₃, 79–821 ppm Sr) often in thin-section scale and even in single crystals. Two amphibole populations were observed in the dacite: low-Al hornblendes represent a cold (<800 °C) silicic crystal mush, whereas the high-Al pargasites crystallized in a hot (>900 °C) mafic magma. Amphibole thermobarometry suggests that the silicic crystal mush was stored in an upper crustal storage (~8–12 km). This was also the place where the erupted dacitic magma was formed during the remobilization of upper crustal silicic crystal mush body by hot mafic magma indicated by simple-zoned and composite amphiboles. This includes reheating (by ~200 °C) and partial remelting of different parts of the crystal mush followed by intensive crystallization of the second mineral population (including pargasites). Breakdown textures of amphiboles imply that they were formed by reheating in case of hornblendes, suggesting that pre-eruptive heating and mixing could take place within days or weeks before the eruption. The decompression rim of pargasites suggests around 12 days of magma ascent in the conduit. Several arc volcanoes produce mixed intermediate magmas with similar bimodal amphibole cargo as the Ciomadul, but in our dacite the two amphibole population can be found even in a single crystal (composite amphiboles). Our study indicates that high-Al pargasites form as a second generation in these magmas after the mafic replenishment into a silicic capture zone; thus, they cannot unambiguously indicate a deeper mafic storage zone beneath these volcanoes. The simple-zoned and composite amphiboles provide direct evidence that significant compositional variations of amphiboles do not necessarily mean variation in the pressure of crystallization even if the Al-tschermak substitution can be recognized, suggesting that amphibole barometers that consider only amphibole composition may often yield unrealistic pressure variation.     

A petrological and geochemical study on time-series samples from Klyuchevskoy volcano,Kamchatka arc

To understand the generation and evolution of mafic magmas from Klyuchevskoy volcano in the Kamchatka arc, which is one of the most active arc volcanoes on Earth, a petrological and geochemical study was carried out on time-series samples from the volcano. The eruptive products show significant variations in their whole-rock compositions (52.0–55.5 wt.% SiO₂), and they have been divided into high-Mg basalts and high-Al andesites. In the high-Mg basalts, lower-K and higher-K primitive samples (>9 wt.% MgO) are present, and their petrological features indicate that they may represent primary or near-primary magmas. Slab-derived fluids that induced generation of the lower-K basaltic magmas were less enriched in melt component than those associated with the higher-K basaltic magmas, and the fluids are likely to have been released from the subducting slab at shallower levels for the lower-K basaltic magmas than for higher-K basaltic magmas. Analyses using multicomponent thermodynamics indicates that the lower-K primary magma was generated by ~13% melting of a source mantle with ~0.7 wt.% H₂O at 1245–1260?°C and ~1.9 GPa. During most of the evolution of the volcano, the lower-K basaltic magmas were dominant; the higher-K primitive magma first appeared in AD 1932. In AD 1937–1938, both the lower-K and higher-K primitive magmas erupted, which implies that the two types of primary magmas were present simultaneously and independently beneath the volcano. The higher-K basaltic magmas evolved progressively into high-Al andesite magmas in a magma chamber in the middle crust from AD 1932 to ~AD 1960. Since then, relatively primitive magma has been injected continuously into the magma chamber, which has resulted in the systematic increase of the MgO contents of erupted materials with ages from ~AD 1960 to present.     

The importance of fractional crystallization and magma mixing in controlling chemical differentiation at Süphan stratovolcano,eastern Anatolia,Turkey

Süphan is a 4,050 m high Pleistocene-age stratovolcano in eastern Anatolia, Turkey, with eruptive products consisting of transitional calc-alkaline to mildly alkaline basalts through trachyandesites and trachytes to rhyolites. We investigate the relative contributions of fractional crystallization and magma mixing to compositional diversity at Süphan using a combination of petrology, geothermometry, and melt inclusion analysis. Although major element chemistry shows near-continuous variation from basalt to rhyolite, mineral chemistry and textures indicate that magma mixing played an important role. Intermediate magmas show a wide range of pyroxene, olivine, and plagioclase compositions that are intermediate between those of basalts and rhyolites. Mineral thermometry of the same rocks yields a range of temperatures bracketed by rhyolite (~750°C) and basalt (~1,100°C). The linear chemical trends shown for most major and trace elements are attributed to mixing processes, rather than to liquid lines of descent from a basaltic parent. In contrast, glassy melt inclusions, hosted by a wide range of phenocryst types, display curved trends for most major elements, suggestive of fractional crystallization. Comparison of these trends to experimental data from basalts and trachyandesites of similar composition to those at Süphan indicates that melt inclusions approximate true liquid lines of descent from a common hydrous parent at pressures of ~500 MPa. Thus, the erupted magmas are cogenetic, but were generated at depths below the shallow, pre-eruptive magma storage region. We infer that chemical differentiation of a mantle-derived basalt occurred in the mid- to lower crust beneath Süphan. A variety of more and less evolved melts with ≥55 wt% SiO₂ then ascended to shallow level where they interacted. The presence of glomerocrysts in many lavas suggests that cogenetic plutonic rocks were implicated in the interaction process. Blending of diverse, but cogenetic, minerals, and melts served to obscure the true liquid lines of descent in bulk rocks. The fact that chemical variation in melt inclusions preserves deep-seated chemical differentiation indicates that inclusions were trapped in phenocrysts prior to shallow-level blending. Groundmass glasses evolved after mixing and display trends that are distinct from those of melt inclusions.     

Insights into silicic melt generation using plagioclase, quartz and melt inclusions from the caldera-forming Rotoiti eruption, Taupo volcanic zone, New Zealand

The Rotoiti (~120 km³) and Earthquake Flat (~10 km³) eruptions occurred in close succession from the Okataina Volcanic Centre at ~50 ka. While accessory mineral geochronology points to long periods of crystallization prior to eruption (10⁴–10⁵ years) and separate thermal histories for the magmas, little was known about the rates and processes of the final melt production and eruption. Crystal zoning patterns in plagioclase and quartz reveal the thermal and compositional history of the magmatic system leading up to the eruption. The dominant modal phase, plagioclase, displays considerable within-crystal zonation: An_37–74, ~40–227 ppm MgO, 45–227 ppm TiO₂, 416–910 ppm Sr and 168–1164 ppm Ba. Resorption horizons in the crystals are marked by sharp increases (10–30%) in Sr, MgO and X_An that reflect changes in melt composition and are consistent with open system processes. Melt inclusions display further evidence for open system behaviour, some are depleted in Sr and Ba relative to accompanying matrix glass not consistent with crystallization of modal assemblage. MI also display a wide range in XH₂O that is consistent with volatile fluxing. Quartz CL images reveal zoning that is truncated by resorption, and accompanied by abrupt increases in Ti concentration (30–80 ppm) that reflect temperature increases ~50–110°C. Diffusion across these resorption horizons is restricted to zones of <20 μm, suggesting most crystallization within the magma occurred in <2000 years. These episodes are brief compared to the longevity (10⁴–10⁵ year) of the crystal mush zones. All textural and compositional features observed within the quartz and plagioclase crystals are best explained by periodic mafic intrusions repeatedly melting parts of a crystal-rich zone and recharging the system with silicic melt. These periodic influxes of silicic melt would have accumulated to form the large volume of magma that fed the caldera-forming Rotoiti eruption.     

Geochemical constraints on the origin of mafic and silicic magmas at Cordón El Guadal, Tatara-San Pedro Complex, central Chile

The aim of this study is to quantify the crustal differentiation processes and sources responsible for the origin of basaltic to dacitic volcanic rocks present on Cordón El Guadal in the Tatara-San Pedro Complex (TSPC). This suite is important for understanding the origin of evolved magmas in the southern Andes because it exhibits the widest compositional range of any unconformity-bound sequence of lavas in the TSPC. Major element, trace element, and Sr-isotopic data for the Guadal volcanic rocks provide evidence for complex crustal magmatic histories involving up to six differentiation mechanisms. The petrogenetic processes for andesitic and dacitic lavas containing undercooled inclusions of basaltic andesitic and andesitic magma include: (1) assimilation of garnet-bearing, possibly mafic lower continental crust by primary mantle-derived basaltic magmas; (2) fractionation of olivine + clinopyroxene + Ca-rich plagioclase + Fe-oxides in present non-modal proportions from basaltic magmas at ∼4–8 kbar to produce high-Al basalt and basaltic andesitic magmas; (3) vapor-undersaturated (i.e., P _H2O<P _TOTAL) partial melting of gabbroic crustal rocks at ∼3–7 kbar to produce dacitic magmas; (4) crystallization of plagioclase-rich phenocryst assemblages from dacitic magmas in shallow reservoirs; (5) intrusion of basaltic andesitic magmas into shallow reservoirs containing crystal-rich dacitic magmas and subsequent mixing to produce hybrid basaltic andesitic and andesitic magmas; and (6)␣formation and disaggregation of undercooled basaltic andesitic and andesitic inclusions during eruption from shallow chambers to form commingled, mafic inclusion-bearing andesitic and dacitic lavas flows. Collectively, the geochemical and petrographic features of the Guadal volcanic rocks are interpreted to reflect the development of shallow silicic reservoirs within a region characterized by high crustal temperatures due to focused basaltic activity and high magma supply rates. On the periphery of the silicic system where magma supply rates and crustal temperatures were lower, cooling and crystallization were more important than bulk crustal melting or assimilation. Received: 2 July 1997 / Accepted: 25 November 1997     

Mixing and differentiation in the Oruanui rhyolitic magma, Taupo, New Zealand: evidence from volatiles and trace elements in melt inclusions

Large pyroclastic rhyolites are snapshots of evolving magma bodies, and preserved in their eruptive pyroclasts is a record of evolution up to the time of eruption. Here we focus on the conditions and processes in the Oruanui magma that erupted at 26.5 ka from Taupo Volcano, New Zealand. The 530 km³ (void-free) of material erupted in the Oruanui event is comparable in size to the Bishop Tuff in California, but differs in that rhyolitic pumice and glass compositions, although variable, did not change systematically with eruption order. We measured the concentrations of H₂O, CO₂ and major and trace elements in zoned phenocrysts and melt inclusions from individual pumice clasts covering the range from early to late erupted units. We also used cathodoluminescence imaging to infer growth histories of quartz phenocrysts. For quartz-hosted inclusions, we studied both fully enclosed melt inclusions and reentrants (connecting to host melt through a small opening). The textures and compositions of inclusions and phenocrysts reflect complex pre-eruptive processes of incomplete assimilation/partial melting, crystallization differentiation, magma mixing and gas saturation. ‘Restitic’ quartz occurs in seven of eight pumice clasts studied. Variations in dissolved H₂O and CO₂ in quartz-hosted melt inclusions reflect gas saturation in the Oruanui magma and crystallization depths of ∼3.5–7 km. Based on variations of dissolved H₂O and CO₂ in reentrants, the amount of exsolved gas at the beginning of eruption increased with depth, corresponding to decreasing density with depth. Pre-eruptive mixing of magma with varying gas content implies variations in magma bulk density that would have driven convective mixing. Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.     

Compositional and thermal evolution of olivine-hosted melt inclusions in small-volume basaltic eruptions: a “simple” example from Dotsero Volcano,NW Colorado

Olivine-hosted melt inclusions have been analyzed from the young (4,150 ± 300 ybp) Dotsero basaltic (48.2 wt% SiO₂) lava flow in Northwest Colorado, USA. Silicate melt-inclusion compositions have a bimodal distribution (41–46 wt% SiO₂ and 47–50 wt% SiO₂). Low-Si melt inclusions record high pre-eruptive sulfur concentrations (>1,000 ppm S) and variations in their major- and trace-element compositions appears to be related to shallow assimilation of local basement sandstone. Whole-rock compositions are modeled as a contamination of low-Si inclusion compositions with ~10 wt% sandstone. Host olivine crystallization may have accompanied magma injection into a shallow storage chamber. In contrast to the low-Si melt inclusions, the high-Si population is relatively degassed and records late-stage rapid crystallization either during or post-eruption. Hopper or skeletal olivine grains in conjunction with the bimodal inclusion compositions suggest relatively rapid cooling rates at the time of eruption and inclusion entrapment. Inclusion compositions, in conjunction with mineral textures, therefore provide a more complete picture of shallow magma processes, coupling the relative timing of undercooling and crystallization, assimilation and melt compositional evolution. Most of the inclusion and host textural and compositional data indicates late and very shallow petrogenetic processes and does not appear to record deeper (mid-, lower-crustal) processes.