1,721,016 research outputs found
Anhydrite solubility in differentiated arc magmas
Full text linkThe solubility of anhydrite in differentiated arc magmas was experimentally studied at 200MPa and 800-1000°C over a range of oxygen fugacities, from 0.5 log units above the Ni-NiO buffer to the hematite-magnetite buffer. Anhydrite is stable only at oxidizing conditions (fO2≥Re-ReO2), whereas sulfides only form under reducing conditions. The solubility of anhydrite in the melt ultimately regulates the amount of sulfur available to partition between melt and fluid phase during the eruption. At oxidizing conditions, the solubility product of anhydrite increases with temperature, nbo/t and melt water content. We provide a new calibration of the anhydrite solubility product (KSP=XCaO*XSO3), which reproduces all available experimental data with greatly improved accuracy:lnKSPAnhydrite=8.95-146.5nbot-2.696104T(K)+19.72nbot104T(K)+0.409·H2O(wt.%)In this equation, the molar fractions XCaO and XSO3 in the melt as well as the number of non-bridging oxygen atoms per tetrahedron (nbo/t) are calculated on an anhydrous basis (H2O refers to the melt water content, T is temperature in Kelvin). We apply our model to estimate the sulfur yield of some recent volcanic eruptions and we show that the sulfur yield of the 1991 Mt. Pinatubo dacite eruption was unusually large, because only a small fraction of the sulfur was locked up in anhydrite. In general, high sulfur yields are expected when anhydrite solubility in the melt is high, i.e. for somewhat depolymerized melts. For rhyolitic systems, most of the available sulfur will be locked up in anhydrite, so that even very large eruptions may only have a small effect on global surface temperatures. Our model therefore allows improved predictions of the environmental impact of explosive volcanic eruptions
Fluid-melt partitioning of sulfur in differentiated arc magmas and the sulfur yield of explosive volcanic eruptions
Full text linkThe fluid-melt partitioning of sulfur (DSfluid/melt) in differentiated arc magmas has been experimentally investigated under oxidizing conditions (Re-ReO2 buffer) from 800 to 950°C at 200MPa. The starting glasses ranged in composition from trachyte to rhyolite and were synthesized targeting the composition of the residual melt formed after 10-60% crystallization of originally trachy-andesitic, dacitic and rhyodacitic magmas (Masotta and Keppler, 2015). Fluid compositions were determined both by mass balance and by Raman spectroscopy of fluid inclusions. DSfluid/melt increases exponentially with increasing melt differentiation, ranging from 2 to 15 in the trachytic melt, from 20 to 100 in the dacitic and rhyodacitic melts and from 100 to 120 in the rhyolitic melt. The variation of the DSfluid/melt is entirely controlled by the compositional variation of the silicate melt, with temperature having at most a minor effect within the range investigated. Experiments from this study were used together with data from the literature to calibrate the following model that allows predicting DSfluid/melt for oxidized arc magmas: lnDSfluid/melt=9.2-31.4·nbot-1.8·ASI-29.5·Al#+4.2·Ca#where nbot is the non-bridging oxygen atoms per tetrahedron, ASI is the alumina saturation index, Al# and Ca# are two empirical compositional parameters calculated in molar units (Al#=XAl2O3XSiO2+XTiO2+XAl2O3 and Ca#=XCaOXNa2O+XK2O).The interplay between fluid-melt partitioning and anhydrite solubility determines the sulfur distribution among anhydrite, melt and fluid. At increasing melt polymerization, the exponential increase of the partition coefficient and the decrease of anhydrite solubility favor the accumulation of sulfur either in the fluid phase or as anhydrite. On the other hand, the higher anhydrite solubility and lower partition coefficient for less polymerized melts favor the retention of sulfur in the melt. At equilibrium conditions, these effects yield a maximum of the sulfur fraction in the fluid phase for slightly depolymerized melts (nbot= 0.05-0.15). Our data allow quantitative predictions of the sulfur yield of explosive volcanic eruptions over a wide range of magma compositions
In situ observations of bubble growth in basaltic, andesitic and rhyodacitic melts
Full text linkBubble growth strongly affects the physical properties of degassing magmas and their eruption dynamics. Natural samples and products from quench experiments provide only a snapshot of the final state of volatile exsolution, leaving the processes occurring during its early stages unconstrained. In order to fill this gap, we present in situ high-temperature observations of bubble growth in magmas of different compositions (basalt, andesite and rhyodacite) at 1,100 to 1,240 °C and 0.1 MPa (1 bar), obtained using a moissanite cell apparatus. The data show that nucleation occurs at very small degrees of supersaturaturation (<60 MPa in basalt and andesite, 200 MPa in rhyodacite), probably due to heterogeneous nucleation of bubbles occurring simultaneously with the nucleation of crystals. During the early stages of exsolution, melt degassing is the driving mechanism of bubble growth, with coalescence becoming increasingly important as exsolution progresses. Ostwald ripening occurs only at the end of the process and only in basaltic melt. The average bubble growth rate (G R) ranges from 3.4 × 10-6 to 5.2 × 10-7 mm/s, with basalt and andesite showing faster growth rates than rhyodacite. The bubble number density (N B) at nucleation ranges from 7.9 × 104 mm-3 to 1.8 × 105 mm-3 and decreases exponentially over time. While the rhyodacite melt maintained a well-sorted bubble size distribution (BSD) through time, the BSDs of basalt and andesite are much more inhomogeneous. Our experimental observations demonstrate that bubble growth cannot be ascribed to a single mechanism but is rather a combination of many processes, which depend on the physical properties of the melt. Depending on coalescence rate, annealing of bubbles following a single nucleation event can produce complex bubble size distributions. In natural samples, such BSDs may be misinterpreted as resulting from several separate nucleation events. Incipient crystallization upon cooling of a magma may allow bubble nucleation already at very small degrees of supersaturation and could therefore be an important trigger for volatile release and explosive eruptions. © 2014 Springer-Verlag Berlin Heidelberg
Trace Element Partitioning Between Saline Aqueous Fluids and Subducted Metasediments, and the Origin of the “Sediment Fingerprint” in Arc Magmas
No full textAbstract Isotopic and elemental signatures in arc magmas bear similarities to marine sediments from the forearc. Partial melts of subducted sediments were previously invoked as the predominant carrier of material between the slab and mantle wedge, whereas aqueous fluids were deemed too inefficient at mobilizing trace elements to account for arc magma compositions. However, trace element solubility in aqueous fluids may be significantly affected by the formation of chloride complexes. We introduced NaCl into the sediment‐H2O system, and re‐investigated trace element partitioning between aqueous fluids and metasediments in a series of piston cylinder experiments at 2.5–4.5 GPa and 600–700°C. The diamond trap method was employed to separate the fluids, which were analyzed in the frozen state. Trace element compositions of fluids and all solid phases were obtained by LA‐ICP‐MS. We combined our data with published literature to demonstrate that saline fluids and sediment melts have a comparable efficiency in extracting incompatible elements from subducted sediments, producing similar element fractionation during mobile phase expulsion. Accessory phases such as allanite may only be stable in particularly Rare Earth Elements‐enriched lithologies. The Sr, Pb and Nd isotopic signatures of arc magma suggest that the mantle wedge is infiltrated by mobile phases derived from both the sediment and basalt sections of the subducted oceanic crust. Up to several percent of either sediment‐derived saline fluid or melt can account for the isotopic and elemental compositions of most arc magma. Geochemical similarities between arc magma and forearc sediments are not necessarily evidence of slab melting
Going Beyond Counting First Authors in Author Co-citation Analysis
Full text linkThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Variations on the Author
Full text link“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
Full text linkWe provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Dispelling the Myths Behind First-author Citation Counts
Full text linkWe conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued
use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation
counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more
sophisticated methods
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