1,720,962 research outputs found
Cold subduction of oceanic crust: Implications from a lawsonite eclogite from the Dominican Republic
Lawsonite eclogite is a rare rock type that has been described from only five natural occurrences. In contrast, laboratory experiments and thermal models predict that lawsonite eclogite should be widespread in subducted oceanic crust deeper than 1.5 GPa. Here we report a new lawsonite eclogite find from the Dominican Republic that provides constraints on the conditions of subducted crust and on its return to the surface. In this sample, lawsonite coexisting with omphacite occurs as both inclusions in garnet and as porphyroblasts, the latter being partly replaced at their margins by epidote and zoisite. Peak pressure conditions estimated from lawsonite-phengite-omphacite-garnet assemblages were ca 1.6 GPa at a temperature of 360degreesC, implying formation under a geotherm of ca. 8degreesC/km. Peak temperature conditions of 410-450degreesC were in the zoisite eclogite field, suggesting that the sample crossed from the stability field of lawsonite eclogite into that of zoisite eclogite as a result of increasing temperature. A comparison with other reported occurrences indicates that most lawsonite eclogite exhumed at the Earth's surface formed in accretionary wedges. The rarity of lawsonite eclogite at the Earth's surface may be principally due to two factors: (i) that in 'normal' subduction settings lawsonite eclogite enters the subduction factory and hence is usually not exhumed; and (ii) that in accretionary wedge settings, where the PT path leaves the stability field of lawsonite eclogite due to heating, lawsonite eclogite is only preserved if the exhumation path is constrained to a narrow window where the terminal stability of lawsonite is not crossed
Going Beyond Counting First Authors in Author Co-citation Analysis
The 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
“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
We 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
We 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
A crystal chemical re-evaluation of amphibole/melt and amphibole/clinopyroxene D-Ti values in petrogenetic studies
Constraints on the calculation and use of mineral/melt and two-mineral partition coefficients for Ti (D-Ti) have been derived from current knowledge of the distinct crystal-chemical mechanisms for the incorporation of Ti4+ in the amphibole structure as follows: (1) mineral/melt partition coefficients for Ti, and other tetravalent high field-strength elements (HFSE), can be compared only when considering the fraction of Ti4+ that enters the same structural site; (2) accurate two-mineral partition coefficients can be obtained only when considering the fraction of Ti4+ that is involved in the same crystal-chemical mechanism in the two relevant phases (i.e., Ti-M2(4+) and Ti-M1(4+) for amphibole and clinopyroxene, respectively). The complete crystal-chemical characterization of synthetic titanian pargasite and kaersutite and of synthetic richterite tall crystallized under P, T, X, f(O2) conditions of interest for upper-mantle studies) shows that the site preference of Zr and Hf differs between the two amphibole compositions; these elements are essentially ordered at M2 in pargasite and kaersutite, but preferentially enter M1 in richterite. In the latter case, Ti segregates into the split M1' site with distorted coordination and shorter Ti-O3 distances, whereas Zr and Hf most likely prefer the larger and more regular M1 site. The observed site preference is strongly controlled by the relative dimensions of the available sites. The crystal-chemical mechanisms that govern the incorporation of octahedral high-charge cations are the local charge balance of Al-[IV] (by R-3,R-4+ at M2) and of dehydrogenation (by R-3,R-4+ at M1); thus the incorporation of Zr and Hf depends on distinct intensive parameters in the two amphibole compositions. Calculation of partition coefficients and of elastic-site parameters under the assumption that all Ti and other HFSE4+ order at the M2 site in amphibole, as is currently done in geochemical studies, is strongly biased. In the presence of significant dehydrogenation, amphibole/melt D-0 values obtained from modeling based on the elastic-strain theory starting from the more-accurate site populations for Ti may be only 1/4 of those obtained by using the total Ti content, and the derived site parameters E and r(0) are more consistent with octahedral coordination. This result has important consequences for the prediction of D values under P-T conditions different from those of the experimental work. Applying the above concepts to data from natural assemblages, we obtained a significantly narrower (0.3-2.4 vs. 1.5-8.9) and more reasonable range of variation for amphibole/clinopyroxene D-Ti. A relationship between these values for D, and pressure is also now apparent
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