The geochemical and petrological characteristics of prenatal caldera volcano: a case of the newly formed small dacitic caldera,Hijiori, Northeast Japan     

Isoji?MiyagiEmail authorView author&#;s OrcID profile  Noriko?Kita  Yuichi?Morishita 《Contributions to Mineralogy and Petrology》2017,172(9):79

Evaluating the magma depth and its physical properties is critical to conduct a better geophysical assessment of magma chambers of caldera volcanoes that may potentially cause future volcanic hazards. To understand pre-eruptive conditions of a magma chamber before its first appearance at the surface, this paper describes the case of Hijiori caldera volcano in northeastern Japan, which emerged approximately 12,000 years ago at a place where no volcano ever existed. We estimated the depth, density, bulk modulus, vesicularity, crystal content, and bulk H\(_2\)O content of the magma chamber using petrographic interpretations, bulk and microchemical compositions, and thermodynamic calculations. The chemical mass balance calculations and thermodynamic modeling of the erupted magmas indicate that the upper portion of the Hijiori magmatic plumbing system was located at depths between 2 and 4 km, and had the following characteristics: (1) pre-eruptive temperature: about 780 \(^{\circ }\)C; (2) bulk magma composition: 66 ± 1.5 wt% SiO\(_{2}\); (3) bulk magmatic H\(_2\)O: approximately 2.5 wt%, and variable characteristics that depend on depth; (4) crystal content: \(\le\)57 vol%; (5) bulk modulus of magma: 0.1–0.8 GPa; (6) magma density: 1.8–2.3 g/cm³; and (7) amount of excess magmatic H\(_2\)O: 11–32 vol% or 48–81 mol%. The range of melt water contents found in quartz-hosted melt inclusions (2–9 wt%) suggests the range of depth phenocrysts growth to be wide (2\(\sim\)13 km). Our data suggest the presence of a vertically elongated magma chamber whose top is nearly solidified but highly vesiculated; this chamber has probably grown and re-mobilized by repeated injections of a small amount of hot dacitic magma originated from the depth.  相似文献   

Reaction-induced grain boundary cracking and anisotropic fluid flow during prograde devolatilization reactions within subduction zones     

Atsushi?OkamotoEmail author  Hiroyuki?Shimizu  Jun-ichi?Fukuda  Jun?Muto  Takamoto?Okudaira 《Contributions to Mineralogy and Petrology》2017,172(9):75

Devolatilization reactions during prograde metamorphism are a key control on the fluid distribution within subduction zones. Garnets in Mn-rich quartz schist within the Sanbagawa metamorphic belt of Japan are characterized by skeletal structures containing abundant quartz inclusions. Each quartz inclusion was angular-shaped, and showed random crystallographic orientations, suggesting that these quartz inclusions were trapped via grain boundary cracking during garnet growth. Such skeletal garnet within the quartz schist formed related to decarbonation reactions with a positive total volume change (?V _t > 0), whereas the euhedral garnet within the pelitic schists formed as a result of dehydration reaction with negative ?V _t values. Coupled hydrological–chemical–mechanical processes during metamorphic devolatilization reactions were investigated by a distinct element method (DEM) numerical simulation on a foliated rock that contained reactive minerals and non-reactive matrix minerals. Negative ?V _t reactions cause a decrease in fluid pressure and do not produce fractures within the matrix. In contrast, a fluid pressure increase by positive ?V _t reactions results in hydrofracturing of the matrix. This fracturing preferentially occurs along grain boundaries and causes episodic fluid pulses associated with the development of the fracture network. The precipitation of garnet within grain boundary fractures could explain the formation of the skeletal garnet. Our DEM model also suggests a strong influence of reaction-induced fracturing on anisotropic fluid flow, meaning that dominant fluid flow directions could easily change in response to changes in stress configuration and the magnitude of differential stress during prograde metamorphism within a subduction zone.  相似文献   

How do granitoid magmas mix with each other? Insights from textures,trace element and Sr–Nd isotopic composition of apatite and titanite from the Matok pluton (South Africa)     

Oscar?LaurentEmail author  Armin?Zeh  Axel?Gerdes  Arnaud?Villaros  Katarzyna?Gros  Ewa?S?aby 《Contributions to Mineralogy and Petrology》2017,172(9):80

In plutonic systems, magma mixing is often modelled by mass balance based on whole-rock geochemistry. However, magma mixing is a chaotic process and chemical equilibration is controlled by non-linear diffusive–advective processes unresolved by the study of bulk samples. Here we present textural observations, LA-(MC-)ICP-MS trace element and Sr–Nd isotopic data of accessory apatites and titanites from a hybrid granodiorite of the Neoarchean Matok pluton (South Africa), collected in a zone of conspicuous mixing between mafic and felsic magmas. Apatite grains mostly show a pronounced zoning in CL images, corresponding to abrupt changes in REE and HFSE concentrations recording their transfer through compositionally different melt domains during mixing. These grains crystallized early, at temperatures of 950–1000 °C. Titanite grains crystallized at temperatures of 820–900 °C (Zr-in-sphene thermometry). They show limited intra-grain chemical variations but huge inter-grain compositional scatter in REE and HFSE, pinpointing crystallization within a crystal mush, from isolated melt pockets having different composition from one another owing to incomplete chemical homogenization and variable Rayleigh fractionation. These chemical–textural characteristics, in combination with partitioning models and Polytopic Vector Analysis, point to “self-mixing” between co-genetic dioritic and granodioritic/granitic magmas. Both resulted from differentiation of mantle-derived mafic melts, showing that mixing does not necessarily involve magmas from contrasted (crust vs. mantle) sources. Systematic variations in εNd _t (?4.5 to ?2.5) and ⁸⁷Sr/⁸⁶Sr_(i) (0.703–0.707) of titanite and apatite grains/domains crystallized from the two magmas point to an isotopically inhomogeneous mantle source, which is not resolved by bulk-rock isotopic data. Interaction between the two magmas must have occurred at relatively high temperatures (ca. 900°C) so that their viscosity contrast remained low, allowing efficient mechanical mixing. Despite this, chemical homogenization was incomplete, as recorded by diffusive fractionation between REE–HFSE and Sr. Modelling thereof reveals that chemical exchange between the liquid phases of the two mixed magmas did not last more than a few tens to hundreds of years. The chemical equilibration between mixed magmas thus strongly depends on the considered elements and observational length scales.  相似文献   

Correction to: The effect of CO<Subscript>2</Subscript> and N<Subscript>2</Subscript> on phase relations,fluid composition,and quartz solubility in amphibolite facies metamorphic rocks     

Margaret?V.?ArtimenkoEmail author 《Contributions to Mineralogy and Petrology》2017,172(11-12):91

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Effects of CO<Subscript>2</Subscript> flushing on crystal textures and compositions: experimental evidence from recent K-trachybasalts erupted at Mt. Etna     

Marisa?Giuffrida  Francois?Holtz  Francesco?Vetere  Marco?ViccaroEmail author 《Contributions to Mineralogy and Petrology》2017,172(11-12):90

Changes in magmatic assemblages and crystal stability as a response of CO₂-flushing in basaltic systems have rarely been directly addressed experimentally, making the role of CO₂ in magma dynamics still controversial and object of scientific debate. We conducted a series of experiments to understand the response of magmas from Etna volcano to CO₂ flushing. We performed a first experiment at 300 MPa to synthesize a starting material composed of crystals of some hundreds of µm and melt pools. This material is representative of an initial magmatic assemblage composed of plagioclase, clinopyroxene and a water-undersaturated melt with 1.6 wt% H₂O. In a second step, the initial assemblage was equilibrated at 300 and 100 MPa with fluids having different XCO ₂ ^fl (CO₂/(H₂O + CO₂)). At low XCO ₂ ^fl (< 0.2 to 0.4), plagioclase is completely dissolved and clinopyroxene show dissolution textures. For relatively high XCO ₂ ^fl (0.9 at 300 MPa), the flushing of a CO₂-rich fluid phase leads to an increase of the amount of clinopyroxene and a decrease of the abundance of plagioclase at 300 MPa. This decrease of plagioclase proportion is associated with a change in An content. Our experiments demonstrate that flushing basaltic systems with fluids may drastically affect crystal textures and phase equilibria depending on proportions of H₂O and CO₂ in the fluid phase. Since texture and crystal proportions are among the most important parameters governing the rheology of magmas, fluid flushing will also influence magma ascent to the Earth’s surface. The experimental results open new perspectives to decipher the textural and compositional record of minerals observed in volcanic rocks from Mt. Etna, and at the same time offer the basis for interpreting the information preserved in minerals from other basaltic volcanoes erupting magmas enriched in CO₂.  相似文献   

High temperature gas–solid reactions in calc–silicate Cu–Au skarn formation; Ertsberg,Papua Province,Indonesia     

Richard?W.?HenleyEmail authorView author&#;s OrcID profile  Frank?J.?Brink  Penelope?L.?King  Clyde?Leys  Jibamitra?Ganguly  Terrance?Mernagh  Jill?Middleton  Christian?J.?Renggli  Melanie?Sieber  Ulrike?Troitzsch  Michael?Turner 《Contributions to Mineralogy and Petrology》2017,172(11-12):106

The 2.7–3 Ma Ertsberg East Skarn System (Indonesia), adjacent to the giant Grasberg Porphyry Copper deposit, is part of the world’s largest system of Cu–Au skarn deposits. Published fluid inclusion and stable isotope data show that it formed through the flux of magma-derived fluid through contact metamorphosed carbonate rock sequences at temperatures well above 600° C and pressures of less than 50 MPa. Under these conditions, the fluid has very low density and the properties of a gas. Combining a range of micro-analytical techniques, high-resolution QEMSCAN mineral mapping and computer-assisted X-ray micro-tomography, an array of coupled gas–solid reactions may be identified that controlled reactive mass transfer through the ~ 1 km³ hydrothermal skarn system. Vacancy-driven mineral chemisorption reactions are identified as a new type of reactive transport process for high-temperature skarn alteration. These gas–solid reactions are maintained by the interaction of unsatisfied bonds on mineral surfaces and dipolar gas-phase reactants such as SO₂ and HCl that are continuously supplied through open fractures and intergranular diffusion. Principal reactions are (a) incongruent dissolution of almandine-grossular to andradite and anorthite (an alteration mineral not previously recognized at Ertsberg), and (b) sulfation of anorthite to anhydrite. These sulfation reactions also generate reduced sulfur with consequent co-deposition of metal sulfides. Diopside undergoes similar reactions with deposition of Fe-enriched pyroxene in crypto-veins and vein selvedges. The loss of calcium from contact metamorphic garnet to form vein anhydrite necessarily results in Fe-enrichment of wallrock, and does not require Fe-addition from a vein fluid as is commonly assumed.  相似文献   

Petrological and experimental evidence for differentiation of water-rich magmas beneath St. Kitts,Lesser Antilles     

Elena?MelekhovaEmail author  Jon?Blundy  Rita?Martin  Richard?Arculus  Michel?Pichavant 《Contributions to Mineralogy and Petrology》2017,172(11-12):98

St. Kitts lies in the northern Lesser Antilles, a subduction-related intraoceanic volcanic arc known for its magmatic diversity and unusually abundant cognate xenoliths. We combine the geochemistry of xenoliths, melt inclusions and lavas with high pressure–temperature experiments to explore magma differentiation processes beneath St. Kitts. Lavas range from basalt to rhyolite, with predominant andesites and basaltic andesites. Xenoliths, dominated by calcic plagioclase and amphibole, typically in reaction relationship with pyroxenes and olivine, can be divided into plutonic and cumulate varieties based on mineral textures and compositions. Cumulate varieties, formed primarily by the accumulation of liquidus phases, comprise ensembles that represent instantaneous solid compositions from one or more magma batches; plutonic varieties have mineralogy and textures consistent with protracted solidification of magmatic mush. Mineral chemistry in lavas and xenoliths is subtly different. For example, plagioclase with unusually high anorthite content (An_≤100) occurs in some plutonic xenoliths, whereas the most calcic plagioclase in cumulate xenoliths and lavas are An₉₇ and An₉₅, respectively. Fluid-saturated, equilibrium crystallisation experiments were performed on a St. Kitts basaltic andesite, with three different fluid compositions (XH₂O = 1.0, 0.66 and 0.33) at 2.4 kbar, 950–1025 °C, and fO₂ = NNO ? 0.6 to NNO + 1.2 log units. Experiments reproduce lava liquid lines of descent and many xenolith assemblages, but fail to match xenolith and lava phenocryst mineral compositions, notably the very An-rich plagioclase. The strong positive correlation between experimentally determined plagioclase-melt Kd_Ca–Na and dissolved H₂O in the melt, together with the occurrence of Al-rich mafic lavas, suggests that parental magmas were water-rich (> 9 wt% H₂O) basaltic andesites that crystallised over a wide pressure range (1.5–6 kbar). Comparison of experimental and natural (lava, xenolith) mafic mineral composition reveals that whereas olivine in lavas is predominantly primocrysts precipitated at low-pressure, pyroxenes and spinel are predominantly xenocrysts formed by disaggregation of plutonic mushes. Overall, St. Kitts xenoliths and lavas testify to mid-crustal differentiation of low-MgO basalt and basaltic andesite magmas within a trans-crustal, magmatic mush system. Lower crustal ultramafic cumulates that relate parental low-MgO basalts to primary, mantle -derived melts are absent on St. Kitts.  相似文献   

CrystalMom: a new model for the evolution of crystal size distributions in magmas with the quadrature-based method of moments     

Colucci?SimoneEmail authorView author&#;s OrcID profile  de’?Michieli?Vitturi?Mattia  Landi?Patrizia 《Contributions to Mineralogy and Petrology》2017,172(11-12):100

Nucleation and growth of crystals, and the resulting crystal size distribution, play a fundamental role in controlling the physical properties of magmas and consequently the dynamics of the eruptions. In the past decades, laboratory experiments demonstrated that size and shape of crystals strongly control the physical properties of magma and lava. Additionally, natural and experimental samples are usually characterized in terms of their crystal size distribution to link it with physical processes that are not directly observable, such as cooling or decompression mechanisms. In this paper, we present CrystalMoM, a new predictive model, based on the quadrature-based method of moments, developed for studying the kinetic of crystallization in volcanic systems. The quadrature-based method of moments, well established in the field of chemical engineering, represents a mesoscale modelling approach that rigorously simulates the space–time evolution of a distribution of particles, by considering its moments. The method is applied here, for the first time, for studying the equilibrium/disequilibrium crystallization in magma, modelling the temporal evolution of the moments of a crystal size distribution. The model, verified against numerical and experimental data, represents a valuable tool to infer the cooling and decompression rates from the crystal size distribution observed in natural samples.  相似文献   

Abyssal and hydrated mantle wedge serpentinised peridotites: a comparison of the 15$$^\circ$$20$$'$$′N fracture zone and New Caledonia serpentinites     

Fiona?Elizabeth?Mothersole  Katy?EvansEmail authorView author&#;s OrcID profile  B.?Ronald?Frost 《Contributions to Mineralogy and Petrology》2017,172(8):69

Subduction of serpentinised mantle transfers oxidised and hydrated mantle lithosphere into the Earth, with consequences for the oxidation state of sub-arc mantle and the genesis of arc-related ore deposits. The role of subducted serpentinised mantle lithosphere in earth system processes is uncertain because subduction fluxes are poorly constrained. Most subducted serpentinised mantle is serpentinised on the ocean floor settings. Yet this material is poorly represented in the literature because it is difficult to access. Large volumes of accessible serpentinite are available in ophiolite complexes, and most interpretations of subduction fluxes associated with ultramafic rocks are based on ophiolite studies. Seafloor and ophiolite serpentinisation can occur under different conditions, so it is necessary to assess if ophiolite serpentinites are a good proxy for seafloor serpentinites. Serpentinites sampled during ODP cruise 209 were compared with serpentinites from New Caledonia. The ODP209 serpentinites were serpentinised by modified seawater in a shallow hydrothermal seafloor setting. The New Caledonia serpentinites were serpentinised in a mantle wedge setting by slab-derived fluids, with possible contributions from oceanic serpentinisation and post-obduction serpentinisation. Petrological, whole rock and mineralogical analyses were combined to compare the two sample sets. Petrologically, the evolution of serpentinisation was close to identical in the two environments. However, more oxidised iron, Cl, S and C is present in serpentine from the ODP209 serpentinites relative to the New Caledonia serpentinites. Given these observations, the use of serpentinites from different geodynamic settings as a proxy for abyssal serpentinites from spreading settings must be undertaken with caution.  相似文献   

Monazite trumps zircon: applying SHRIMP U–Pb geochronology to systematically evaluate emplacement ages of leucocratic,low-temperature granites in a complex Precambrian orogen     

Agnieszka?M.?PiechockaEmail authorView author&#;s OrcID profile  Courtney?J.?Gregory  Jian-Wei?Zi  Stephen?Sheppard  Michael?T.?D.?Wingate  Birger?Rasmussen 《Contributions to Mineralogy and Petrology》2017,172(8):63

Although zircon is the most widely used geochronometer to determine the crystallisation ages of granites, it can be unreliable for low-temperature melts because they may not crystallise new zircon. For leucocratic granites U–Pb zircon dates, therefore, may reflect the ages of the source rocks rather than the igneous crystallisation age. In the Proterozoic Capricorn Orogen of Western Australia, leucocratic granites are associated with several pulses of intracontinental magmatism spanning ~800 million years. In several instances, SHRIMP U–Pb zircon dating of these leucocratic granites either yielded ages that were inconclusive (e.g., multiple concordant ages) or incompatible with other geochronological data. To overcome this we used SHRIMP U–Th–Pb monazite geochronology to obtain igneous crystallisation ages that are consistent with the geological and geochronological framework of the orogen. The U–Th–Pb monazite geochronology has resolved the time interval over which two granitic supersuites were emplaced; a Paleoproterozoic supersuite thought to span ~80 million years was emplaced in less than half that time (1688–1659 Ma) and a small Meso- to Neoproterozoic supersuite considered to have been intruded over ~70 million years was instead assembled over ~130 million years and outlasted associated regional metamorphism by ~100 million years. Both findings have consequences for the duration of associated orogenic events and any estimates for magma generation rates. The monazite geochronology has contributed to a more reliable tectonic history for a complex, long-lived orogen. Our results emphasise the benefit of monazite as a geochronometer for leucocratic granites derived by low-temperature crustal melting and are relevant to other orogens worldwide.  相似文献