Episodic tourmaline growth and re-equilibration in mica pegmatite from the Bihar Mica Belt, India: major- and trace-element variations under pegmatitic and hydrothermal conditions

2016 ◽  
Vol 154 (1) ◽  
pp. 68-86 ◽  
Author(s):  
PRANJIT HAZARIKA ◽  
DEWASHISH UPADHYAY ◽  
KAMAL LOCHAN PRUSETH
Keyword(s):  
Trace Elements ◽  
Trace Element ◽  
Major Element ◽  
Element Composition ◽  
Coarse Grained ◽  
Partial Replacement ◽  
Type I ◽  
Type Ii ◽  
Hydrothermal Conditions ◽  
Major Element Composition

AbstractMica pegmatites from the Bihar Mica Belt contain three distinct generations of tourmaline. The major-element composition, substitution vectors and trajectories within each group are different, which indicates that the three types of tourmalines are not a part of one evolutionary series. Rather, the differences in their chemistries as well their mutual microtextural relations, can be best explained by growth of tourmaline from pegmatitic melts followed by episodic re-equilibration during discrete geological events. The euhedral, coarse-grained brown type I tourmaline cores have relatively high Ca, Mg (XMgc. 0.37) and Al with correlated variation in Sr, Sc, Ti, Zr, Y, Cr, Pb and Rare Earth elements (REEs). They are inferred to have crystallized from pegmatitic melts. Monazites included within these tourmalines give chemical ages of 1290−1242 Ma interpreted to date the crystallization of the pegmatitic tourmaline. The bluish type II and greyish type III tourmalines with low Ca and Mg contents (XMg = 0.16−0.27) and high Zn, Sn, Nb, Ta and Na, formed by pseudomorphic partial replacement of the pegmatitic tourmaline via fluid-mediated coupled dissolution–reprecipitation, are ascribed to a hydrothermal origin. The ages obtained from monazites included in these tourmalines indicate two alteration events at c. 1100 Ma and c. 950 Ma. The correlated variation of Ca, Mg and Fe and the trace elements Sr, Sn, Sc, Zn and REE within the tourmalines indicates that the trace-element concentrations of tourmaline are controlled not only by the fluid chemistry but also by coupled substitutions with major-element ions.

Kyanite-bearing eclogite xenoliths from the Udachnaya kimberlite, Siberian craton, Russia

2017 ◽  
Vol 188 (1-2) ◽  
pp. 7 ◽  
Author(s):  
Ioana-Bogdana Radu ◽  
Bertrand Moine ◽  
Dmitri Ionov ◽  
Andrey Korsakov ◽  
Alexander Golovin ◽  
...  
Keyword(s):  
Siberian Craton ◽  
Major Element ◽  
Kimberlite Pipe ◽  
West African ◽  
Coarse Grained ◽  
Chemical Compositions ◽  
Type I ◽  
Type Ii ◽  
Major Element Composition ◽  
Subducted Oceanic Crust

Xenoliths brought up by kimberlite magmas are rare samples of otherwise inaccessible lithospheric mantle. Eclogite xenoliths are found in most cratons and commonly show a range of mineral and chemical compositions that can be used to better understand craton formation. This study focuses on five new kyanite-bearing eclogites from the Udachnaya kimberlite pipe (367±5 Ma). They are fine-to coarse-grained and consist mainly of “cloudy” clinopyroxene (cpx) and garnet (grt). The clinopyroxene is Al,Na-rich omphacite while the garnet is Ca-rich, by contrast to typical bi-mineral (cpx+grt) eclogites that contain Fe- and Mg-rich garnets. The Udachnaya kyanite eclogites are similar in modal and major element composition to those from other cratons (Dharwar, Kaapvaal, Slave, West African). The kyanite eclogites have lower REE concentrations than bi-mineral eclogites and typically contain omphacites with positive Eu and Sr anomalies, i.e. a “ghost plagioclase signature”. Because such a signature can only be preserved in nonmetasomatised samples, we infer that they were present in the protoliths of the eclogites. It follows that subducted oceanic crust is present at the base of the Siberian craton. Similar compositions and textures are also seen in kyanite eclogites from other cratons, which we view as evidence for an Archean, subduction-like formation mechanism related to craton accretion. Thus, contrary to previous work that classifies all kyanite eclogites as type I (IK), metasomatized by carbonatite/kimberlitic fluids, we argue that some of them, both from this work and those from other cratons, belong to the non-metasomatized type II (IIB). The pristine type IIB is the nearest in composition to protoliths of mantle eclogites because it contains no metasomatic enrichments.

Provenance of basaltic tephra from Vatnajökull subglacial volcanoes, Iceland, as determined by major- and trace-element analyses

The Holocene ◽  
2011 ◽  
Vol 21 (7) ◽  
pp. 1037-1048 ◽  
Author(s):  
Bergrún Arna Óladóttir ◽  
Olgeir Sigmarsson ◽  
Gudrún Larsen ◽  
Jean-Luc Devidal
Keyword(s):  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Major Element ◽  
Element Composition ◽  
Major Element Composition ◽  
Volcanic System ◽  
The Holocene ◽  
Inductively Coupled ◽  
Ice Cap ◽  
The North

The Holocene eruption history of subglacial volcanoes in Iceland is largely recorded by their tephra deposits. The numerous basaltic tephra offer the possibility to make the tephrochronology in the North Atlantic area more detailed and, therefore, more useful as a tool not only in volcanology but also in environmental and archaeological studies. The source of a tephra is established by mapping its distribution or inferred via compositional fingerprinting, mainly based on major-element analyses. In order to improve the provenance determinations for basaltic tephra produced at Grímsvötn, Bárdarbunga and Kverkfjöll volcanic systems in Iceland, 921 samples from soil profiles around the Vatnajökull ice-cap were analysed for major-element concentrations by electron probe microanalysis. These samples are shown to represent 747 primary tephra units. The tephra erupted within each of these volcanic system has similar chemical characteristics. The major-element results fall into three distinctive compositional groups, all of which show regular decrease of MgO with increasing K2O concentrations. The new analyses presented here considerably improve the compositional distinction between products of the three volcanic systems. Nevertheless, slight overlap of the compositional groups for each system still remains. In situ trace-element analyses by laser-ablation-inductively-coupled-plasma-mass-spectrometry were applied for better provenance identification for those tephra having similar major-element composition. Three trace-element ratios, Rb/Y, La/Yb and Sr/Th, proved particularly useful. Significantly higher La/Yb distinguishes the Grímsvötn basalts from those of Bárdarbunga and Rb/Y values differentiate the basalts of Grímsvötn and Kverkfjöll. Additionally, the products of Bárdarbunga, Grímsvötn and Kverkfjöll form distinct compositional fields on a Sr/Th versus Th plot. Taken together, the combined use of major- and trace-element analyses in delineating the provenance of basaltic tephra having similar major-element composition significantly improves the Holocene tephra record as well as the potential for correlations with tephra from outside Iceland.

Major- and trace-element characterization, expanded distribution, and a new chronology for the latest Pleistocene Glacier Peak tephras in western North America

2009 ◽  
Vol 71 (2) ◽  
pp. 201-216 ◽  
Author(s):  
Stephen C. Kuehn ◽  
Duane G. Froese ◽  
Paul E. Carrara ◽  
Franklin F. Foit ◽  
Nicholas J.G. Pearce ◽  
...  
Keyword(s):  
North America ◽  
Trace Element ◽  
Late Pleistocene ◽  
Major Element ◽  
Element Composition ◽  
Western North America ◽  
Major Element Composition ◽  
Element Abundances ◽  
Southern Alberta ◽  
Tephra Beds

AbstractThe Glacier Peak tephra beds are among the most widespread and arguably some of the most important late Pleistocene chronostratigraphic markers in western North America. These beds represent a series of closely-spaced Plinian and sub-Plinian eruptions from Glacier Peak, Washington. The two most widespread beds, Glacier Peak ‘G’ and ‘B’, are reliably distinguished by their glass major and trace element abundances. These beds are also more broadly distributed than previously considered, covering at least 550,000 and 260,000 km2, respectively. A third bed, the Irvine bed, known only from southern Alberta, is similar in its major-element composition to the Glacier Peak G bed, but it shows considerable differences in trace element concentrations. The Irvine bed is likely considerably older than the G and B tephras and probably records an additional Plinian eruption, perhaps also from Glacier Peak but from a different magma than G through B. A review of the published radiocarbon ages, new ages in this study, and consideration in a Bayesian framework suggest that the widespread G and B beds are several hundred years older than widely assumed. Our revised age is about 11,600 14C yr BP or a calibrated age (at 2 sigma) of 13,710–13,410 cal yr BP.

scholarly journals Some Aspects of Multilayer Ceramic Chip Capacitors for Hybrid Circuits

1978 ◽  
Vol 5 (1) ◽  
pp. 33-40 ◽  
Author(s):  
W. Noorlander
Keyword(s):  
Partial Replacement ◽  
Type I ◽  
Type Ii ◽  
Multilayer Ceramic ◽  
Ceramic Dielectrics ◽  
Silver Palladium

It is shown that both European and American standardization committees specify the dimensions in the same grid and that there is no standardization of the thickness in relation to the capacitance.Of the ceramic dielectrics, special attention is paid to the instability of capacitance and losses of type II materials due to temperature and voltage treatment.The conductivity of the inner electrodes determines the losses at 1 MHz in type I dielectrics. It is shown that the economically interesting partial replacement of Pd by Ag can cause an increase in the losses: other substitute metals seem more promising.The last aspect discussed is the end terminations of the capacitors. In the case of silver/palladium end terminations the Ag/Pd ratio should be smaller than two.

scholarly journals Linking Cellulose Fiber Sediment Methyl Mercury Levels to Organic Matter Decay and Major Element Composition

AMBIO ◽  
2014 ◽  
Vol 43 (7) ◽  
pp. 878-890 ◽  
Author(s):  
Olof Regnell ◽  
Mark Elert ◽  
Lars Olof Höglund ◽  
Anna Helena Falk ◽  
Anders Svensson
Keyword(s):  
Organic Matter ◽  
Methyl Mercury ◽  
Major Element ◽  
Cellulose Fiber ◽  
Element Composition ◽  
Major Element Composition

scholarly journals Multivariate Statistical Analysis of Trace Elements in Pyrite: Prediction, Bias and Artefacts in Defining Mineral Signatures

Minerals ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 61 ◽  
Author(s):  
Marija Dmitrijeva ◽  
Nigel J. Cook ◽  
Kathy Ehrig ◽  
Cristiana L. Ciobanu ◽  
Andrew V. Metcalfe ◽  
...  
Keyword(s):  
Trace Elements ◽  
Statistical Analysis ◽  
Trace Element ◽  
South Australia ◽  
Large Datasets ◽  
Ore Deposits ◽  
Partial Replacement ◽  
Multivariate Statistical ◽  
Wide Range ◽  
Olympic Dam

Pyrite is the most common sulphide in a wide range of ore deposits and well known to host numerous trace elements, with implications for recovery of valuable metals and for generation of clean concentrates. Trace element signatures of pyrite are also widely used to understand ore-forming processes. Pyrite is an important component of the Olympic Dam Cu–U–Au–Ag orebody, South Australia. Using a multivariate statistical approach applied to a large trace element dataset derived from analysis of random pyrite grains, trace element signatures in Olympic Dam pyrite are assessed. Pyrite is characterised by: (i) a Ag–Bi–Pb signature predicting inclusions of tellurides (as PC1); and (ii) highly variable Co–Ni ratios likely representing an oscillatory zonation pattern in pyrite (as PC2). Pyrite is a major host for As, Co and probably also Ni. These three elements do not correlate well at the grain-scale, indicating high variability in zonation patterns. Arsenic is not, however, a good predictor for invisible Au at Olympic Dam. Most pyrites contain only negligible Au, suggesting that invisible gold in pyrite is not commonplace within the deposit. A minority of pyrite grains analysed do, however, contain Au which correlates with Ag, Bi and Te. The results are interpreted to reflect not only primary patterns but also the effects of multi-stage overprinting, including cycles of partial replacement and recrystallisation. The latter may have caused element release from the pyrite lattice and entrapment as mineral inclusions, as widely observed for other ore and gangue minerals within the deposit. Results also show the critical impact on predictive interpretations made from statistical analysis of large datasets containing a large percentage of left-censored values (i.e., those falling below the minimum limits of detection). The treatment of such values in large datasets is critical as the number of these values impacts on the cluster results. Trimming of datasets to eliminate artefacts introduced by left-censored data should be performed with caution lest bias be unintentionally introduced. The practice may, however, reveal meaningful correlations that might be diluted using the complete dataset.

Deconvolution of the composition of fine-grained pyrite in sedimentary matrix by regression of time-resolved LA-ICP-MS data

2020 ◽  
Vol 105 (6) ◽  
pp. 820-832 ◽  
Author(s):  
Aleksandr S. Stepanov ◽  
Leonid V. Danyushevsky ◽  
Ross R. Large ◽  
Indrani Mukherjee ◽  
Irina A. Zhukova
Keyword(s):  
Trace Elements ◽  
Regression Analysis ◽  
Trace Element ◽  
Sedimentary Rocks ◽  
Trace Element Composition ◽  
Element Composition ◽  
Silicate Matrix ◽  
Time Resolved ◽  
Icp Ms ◽  
Wide Range

Abstract Pyrite is a common mineral in sedimentary rocks and is the major host for many chalcophile trace elements utilized as important tracers of the evolution of the ancient hydrosphere. Measurement of trace element composition of pyrite in sedimentary rocks is challenging due to fine-grain size and intergrowth with silicate matrix and other sulfide minerals. In this contribution, we describe a method for calculation of trace element composition of sedimentary pyrite from time-resolved LA-ICP-MS data. The method involves an analysis of both pyrite and pyrite-free sediment matrix, segmentation of LA-ICP-MS spectra, normalization to total, regression analysis of dependencies between the elements, and calculation of normalized composition of the mineral. Sulfur is chosen as an explanatory variable, relative to which all regressions are calculated. The S content value used for calculation of element concentrations from the regressions is calculated from the total, eliminating the need for independent constraints. The algorithm allows efficient measurement of concentrations of multiple chalcophile trace elements in pyrite in a wide range of samples, including quantification of detection limits and uncertainties while excluding operator bias. The data suggest that the main sources of uncertainties in pyrite composition are sample heterogeneity and counting statistics for elements of low abundance. The analysis of regression data of time-resolved LA-ICP-MS measurements could provide new insights into the geochemistry of the sedimentary rocks and minerals. It allows quantification of ratios of elements that do not have reference material available (such as Hg) and provides estimates on the content of non-sulfidic Fe in the silicate matrix. Regression analysis of the mixed LA-ICP-MS signal could be a powerful technique for deconvolution of phase compositions in complex multicomponent samples.

The geochemistry of hydrothermal and pelagic sediments from the Galapagos Hydrothermal Mounds Field, D.S.D.P. Leg 70

1983 ◽  
Vol 47 (344) ◽  
pp. 291-300 ◽  
Author(s):  
S. A. Moorby ◽  
D.S. Cronan
Keyword(s):  
Major Element ◽  
Hydrothermal Solution ◽  
Element Composition ◽  
Pelagic Sediment ◽  
Solution Composition ◽  
Major Element Composition ◽  
Sediment Samples ◽  
Mn Oxide ◽  
Formation Conditions ◽  
Metal Ratios

AbstractOver 200 sediment samples taken from ten holes drilled in the Galapagos Hydrothermal Mounds Field during D.S.D.P. Leg 70 have been analysed for twenty-one elements. The three main sediment lithologies recognized are siliceous carbonate ooze, Mn-oxide crust, and an Fe-rich silicate (nontronite), the latter two being of hydrothermal origin. The major element composition of the hydrothermal deposits is similar in each mound hole, suggesting that formation conditions and hydrothermal solution composition have been constant both geographically and with time. The large variations which occur in the concentration of some trace elements in the Mn-oxide crusts and in transition metal ratios in the nontronite compared with the pelagic ooze suggests a hydrothermal supply to the mounds of Li, Mo, Pb, and Ba in addition to Mn, Fe, and silica.The data are compatible with suggestions that the nontronite formed at depth in the pelagic sediment blanket by replacement of biogenic ooze, whilst the Mn crusts formed at or near the sediment-water interface. Pelagic sediments in the mounds which have not been replaced are similar in composition to pelagic sediments from non-mounds holes.

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