1,720,985 research outputs found
Experimental time constraints on the kinetic and chemistry of amphibole at deep crustal levels
No full textAiming to improve the current knowledge about amphibole growth kinetics at deep crustal levels, new amphibole growth rate data are provided. Our findings, indeed, may be useful to correctly interpret the textural features of amphibole-bearing mafic cumulates and rocks, and for a better constraining of the timescales of magmatic processes at upper mantle-lower crustal depths. Experiments were performed to determine the amphibole growth rates in a primitive alkaline basalt from Procida island (Campi Flegrei Volcanic District, southern Italy) at the following conditions: temperature of 1030 and 1080 °C, pressure of 0.8 GPa, water content in the range 3.3-4.2 wt%, and variable dwell time from 0.25 to 9 h. Amphibole growth rates range from 1.5·10-7 to 2.9·10-8 cm·s-1 with increasing the duration of the experiments. It is observed that, keeping a constant dwell time, an increase of the experimental temperature or of the water content results in comparable growth rate increase. Coexisting synthetic amphibole and clinopyroxene show a faster growth rates in favour of amphibole regardless of the dwell time, since the chemical and structural similarities of these minerals cause kinetic competition. Moreover, the chemical composition of amphibole is influenced mainly by the experimental time; in detail, in the shortest (≤3 h) and low temperature runs edenite is the prevailing composition whereas the magnesiohastingsitic term becomes dominant at higher temperature and longer run duration. Based on the interpretation of the Fe-Mg exchange coefficient values between amphibole and coexisting liquid, the magnesiohastingsitic amphibole is considered to be the stable term at the investigated run conditions. Finally, the resulting growth rates have been applied to constrain the crystallization time of natural amphiboles and clinopyroxenes from the Oligo-Miocene cumulates of north-western Sardinia (i.e., Capo Marargiu Volcanic District, Italy), yielding crystallization times in the range 1.46-3.12 yr
Amphibole growth from a primitive alkaline basalt at 0.8 GPa: Time-dependent compositional evolution, growth rate and competition with clinopyroxene
No full textAmphibole growth rates were experimentally determined at hydrous (3.3-4.2 wt% H2O), isobaric (0.8 GPa) conditions, variable temperature (1030 and 1080 °C) and dwell time (0.25, 3, 6, and 9 h), using as starting material a primitive alkaline basalt from Procida island (Campi Flegrei Volcanic District, south Italy). Amphibole growth rates decrease from 1.5·10-7 to 2.9·10-8 cm·s-1 as the duration of our experiments increase from 0.25 to 9 hours. Moreover, increasing both temperature and water content leads to similar growth rate increase at constant dwell time. The comparison between amphibole and clinopyroxene growth rates determined at the same experimental conditions reveals for amphibole a faster growth relatively to the coexisting clinopyroxene, regardless of the dwell time. Furthermore, the experimental time appears to be a critical parameter for the composition of synthetic amphiboles; specifically, edenite is the dominant composition in short experiments (≤3 h), particularly, at low temperature (1030 °C), whereas the magnesiohastingsitic amphibole becomes progressively more important shifting towards longer duration and higher temperature run conditions. The magnesiohastingsite, on the basis of the amphibole-liquid Fe-Mg exchange coefficient values, results to be the compositional term representative of amphibole-melt equilibrium at the investigated P-T-H2O conditions. Finally, experimental growth rates from this study have been used to investigate the crystallization time of natural amphiboles and clinopyroxenes from the Oligo-Miocene cumulates of north-western Sardinia (i.e. Capo Marargiu Volcanic District, Italy), yielding crystallization times of 1.46-3.12 yr
Sulfur and REE zoning in apatite. The example of the Colli Albani magmatic system
No full textWe investigate the distribution of major and trace elements in apatite crystals hosted in granular alkaline rocks composed mainly of leucite and clinopyroxene, representative of the hypabyssal crystallization of a magma body in the Quaternary ultra-potassic Colli Albani Volcanic District (CAVD), which was emplaced into thick limestone units along the Tyrrhenian margin of Italy. Results show that the analyzed crystals are the SrO-richest (up to 4.6 wt%) fluorapatite (F =2.6-3.7 wt%) of the Italian alkaline rocks. The strontium enrichment is caused by the lack of other Sr-compatible mineral phases, such as plagioclase, alkali feldspar and melilite, in these leucite- and clinopyroxene-bearing rocks. The studied samples show core-rim zoning with rims enriched in Si, S, and REE whereas the cores are enriched in Ca and P. The LREE-oxides contents of apatite, reaching 4.2 wt%, represent more than 95% of the total REE budget; SiO2contents range from 1.3 to 3.6 wt%, and SO3concentrations between 0.6 and 1.4 wt%. We support the idea that REE and sulfur enrichment are a response to the crystallization caused by the pressure drop in the magmatic system during the eruption and follow the substitution mechanisms Si4++ REE3+= P5++ Ca2+and S6++ Si4+= 2P5+. The results also suggest the presence of the substitution Th4++ 2Si4+= Ca2++ 2P5+
Experimental re-melting of a continental crust:probing the deep storage zone of Campi Flegrei and Vesuvius magmas
Full text linkMantle magmas interact with surrounding rocks during their ascent and storage in the continental crust, leading to open system processes as wall rock partial melting. In this study, we have experimentally investigated the reactions between a leucosome depleted migmatite and a primitive K-basaltic of Campi Flegrei (Italy). Experiments were carried out at pressure of 0.8 GPa temperatures from 1250 °C to 1050 °C and constant temperature and thermal gradient conditions. The experimental products consist of biotite-free migmatite, glass and crystals of clinopyroxene, olivine, plagioclase and Cr-spinel with proportions that vary as a function of temperature. Open system isothermal experiments indicate that the chemistry of melts and phase relationships are controlled by the high Al2O3 content of leucosome depleted migmatite with the glass composition shifting from K-trachybasalt towards shoshonite as the temperature decreases from 1200 °C to 1125 °C. At temperatures 1150°C, migmatite assimilation is not exclusively due to the assimilation fractional crystallization process because evidence of mingling and mixing is observed. T-gradient experiment shows melt composition ranging from shoshonite to phono-tephrite moving from the slightly crystalline zone (T = 1250 –1210 °C) at the bottom of the capsule towards the highly crystalline zone (T = 1160 –1140 °C). This SiO2-constant trend indicates that at temperature below the basalt solidus, the assimilation of leucosome depleted crust is represented almost exclusively by the biotite breakdown, leading to the increase in Al, Mg, Fe, Ti, and K activities in the system. The shoshonitic composition obtained in our experiments could represent the parental magma for both Campi Flegrei volcanic district and Vesuvius magmatic systems, indicating modification in a deep storage zone through mixing with the partial melts derived from restitic continental crust.</p
Experimental investigation of trace element partitioning between amphibole and alkali basaltic melt: towards a more general partitioning model with implications for amphibole fractionation at deep crustal levels
Full text linkTime-series experiments were carried out in a piston-cylinder apparatus at 0.8 GPa and 1030–1080 °C using a hydrous K-basalt melt as the starting material to determine the element partition coefficients between amphibole and silicate glass. Major, minor, and trace element compositions of amphibole and glass were determined with a combination of electron microprobe and laser ablation inductively coupled plasma mass spectrometry. Results show that the main mineral phase is calcic amphibole, and the coexisting glass compositions range from basaltic trachyandesite to andesite. We estimated the ideal radius, the maximum partition coefficient and the apparent Young’s modulus of the A, M1-M2-M3, and M4-M4′ sites of amphibole. The influence of melt and amphibole composition, temperature, and pressure on the partition coefficients between amphiboles and glasses has also been investigated by comparing our data with a literature data set spanning a wide range of pressures (0.6–2.5 GPa), temperatures (780–1100 °C), and compositions (from basanite to rhyolite). Finally, we modeled a deep fractional crystallization process using the amphibole-melt partition coefficients determined in this study, observing that significant amounts of amphibole crystallization (>30 wt%) well reproduce the composition of an andesitic melt similar to that of the calc-alkaline volcanic products found in Parete and Castelvolturno boreholes (NW of Campi Flegrei, Italy)
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
Experimental study of monazite solubility in haplogranitic melts: a new model for peraluminous and peralkaline melts
No full textAbstract: Monazite is a common accessory mineral in peraluminous, metaluminous and peralkaline granitic/rhyolitic rocks. Considering the importance of monazite in geochemical and geochronological studies, a monazite solubility model that can be applied to a wide compositional range of magmas is desirable. To accomplish this, monazite solubility experiments were performed at atmospheric (1400 C) and crustal pressures (1–3 kbar, 720–850 C, H2O-saturated), using haplogranitic compositions ranging from peraluminous to peralkaline, doped with synthetic pure LaPO4. The concentrations of La in the melts increase sharply with increasing temperature and peralkalinity of the melt. We combined our new data with those of previous studies to describe the solubility of monazite in peralkaline to peraluminous melts. Our new monazite saturation model, which incorporates temperature, pressure, water content, melt and monazite composition is given by: lnRLREE = 12.77(±0.49) + 1.52(±0.15)M + 22 0.44(±0.10)(H2O)0.5 9934(±632)/T 36.79(±6.15)P/T + lnXLREE mnz where RLREE is the sum of the concentrations of La to Sm in monazite-saturated melt, in ppm, M is a dimensionless compositional parameter (Na + K + 2Ca) · Al1 · (Al + Si)1, similar to the compositional parameter used in an earlier model by Montel; Na, K, Ca, Al, Si are in moles, H2O is water content in weight percent, T is the temperature in K, P is the pressure in kbar, and XLREE mnz is the mole fraction of LREE in monazite LREEmnz/ (LREEmnz + Ymnz + Thmnz + Umnz). This model reproduces 76% and >95% of the data to within uncertainties of ±10% and ±20%, respectively. It may be applied to felsic melts poor in CaO + FeO + MgO (<3 wt%) from peraluminous to peralkaline compositions.
Key-words: monazite; solubility; melt composition; agpaitic index; peralkaline; peraluminous; haplogranite; model; experimental petrology
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