Major Element, REE, and Other Trace Element Behavior in Amphibolite Weathering under Semiarid Conditions in Southern India

2000 ◽  
Vol 108 (4) ◽  
pp. 487-496 ◽  
Author(s):  
Anupam Sharma ◽  
V. Rajamani
Keyword(s):  
Trace Element ◽  
Major Element ◽  
Southern India ◽  
Semiarid Conditions

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 Element, Trace Element, Nutrient, and Radionuclide Mobility in a Mining By-Product-Amended Soil

2012 ◽  
Vol 41 (6) ◽  
pp. 1818-1834 ◽  
Author(s):  
G. Douglas ◽  
J. Adeney ◽  
K. Johnston ◽  
L. Wendling ◽  
S. Coleman
Keyword(s):  
Trace Element ◽  
Major Element ◽  
Amended Soil

XVII.—The Major Ultrabasic and Basic Intrusions of St Kilda, Outer Hebrides

1967 ◽  
Vol 66 (17) ◽  
pp. 419-444 ◽  
Author(s):  
R. R. Harding
Keyword(s):  
Trace Element ◽  
Major Element ◽  
Layered Intrusion ◽  
Fine Grained ◽  
Outer Hebrides ◽  
Crystal Accumulation

AbstractThe structures and mineralogy of the Tertiary ultrabasic and basic intrusions are described. The ultrabasic rocks are thought to be remnants of a layered intrusion which once extended from Hirta to Boreray, and which probably formed by crystal accumulation. The eucrites may represent higher levels of this intrusion. A 350 feet-thick, fine-grained margin is described from the East Glen Bay Gabbro. The metamorphism of the ultrabasic and eucritic rocks, and the formation of the Glacan Mor Complex, probably occurred in a basic environment, before intrusion of the first acid rocks on St. Kilda. Five major-element and twenty-two trace-element analyses are presented.

scholarly journals Miocene and Pliocene Silicic Coromandel Volcanic Zone Tephras from ODP Site 1124-C: Petrogenetic Applications and Temporal Evolution

2021 ◽  
Author(s):  
◽  
Matthew Thomas Stevens
Keyword(s):  
Trace Element ◽  
Mantle Wedge ◽  
Major Element ◽  
Volcanic Glass ◽  
Fractional Crystallisation ◽  
Volcanic Zone ◽  
Arc Magmas ◽  
Glass Shard ◽  
Tephra Layers ◽  
Glass Shards

<p>The Coromandel Volcanic Zone (CVZ) was the longest-lived area of volcanism in New Zealand hosting the commencement of large explosive rhyolitic and ignimbrite forming eruptions. The NW trending Coromandel Peninsula is the subaerial remnant of the Miocene-Pliocene CVZ, which is regarded as a tectonic precursor to the Taupo Volcanic Zone (TVZ), currently the most dynamic and voluminous rhyolitic volcanic centre on Earth. This study presents new single glass shard major and trace element geochemical analyses for 72 high-silica volcanic tephra layers recovered from well-dated deep-sea sediments of the SW Pacific Ocean by the Ocean Drilling Program (ODP) Leg 181. ODP Site 1124, ~720 km south and east from the CVZ, penetrated sediments of the Rekohu Drift yielding an unprecedented record of major explosive volcanic eruptions owing to the favourable location and preservation characteristics at this site. This record extends onshore eruptive sequences of CVZ explosive volcanism that are obscured by poor exposure, alteration, and erosion and burial by younger volcanic deposits. Tephra layers recovered from Site 1124 are well-dated through a combination of biostratigraphic and palaeomagnetic methods allowing the temporal geochemical evolution of the CVZ to be reconstructed in relation to changes in the petrogenesis of CVZ arc magmas from ~ 10 to 2 Ma. This thesis establishes major and trace element geochemical "fingerprints" for all Site 1124-C tephras using well-established (wavelength dispersive electron probe microanalysis) and new (laser ablation inductively coupled plasma mass spectrometry) in situ single glass shard microanalytical techniques. Trace element analysis of Site 1124-C glass shards (as small as 20 um) demonstrate that trace element signatures offer a more specific, unequivocal characterisation for distinguishing (and potentially correlating) between tephras with nearly identical major element compositions. The Site 1124-C core contains 72 unaltered Miocene-Pliocene volcanic glass-shard-bearing laminae > 1 cm thick that correspond to 83 or 84 geochemical eruptive units. Revised eruptive frequencies based on the number of geochemical eruptive units identified represent at least one eruption every 99 kyr for the late Miocene and one per 74 kyr for the Pliocene. The frequency of tephra deposition throughout the history of the CVZ has not been constant, rather reflecting pulses of major explosive eruptions resulting in closely clustered groups of tephra separated by periods of reduced activity, relative volcanic quiescence or non-tephra deposition. As more regular activity became prevalent in the Pliocene, it was accompanied by more silicic magma compositions. Rhyolitic volcanic glass shards are characterised by predominantly calc-alkaline and minor high-K enriched major element compositions. Major element compositional variability of the tephras deposited between 10 Ma and 2 Ma reveals magma batches with pre-eruptive compositional gradients implying a broad control by fractional crystallisation. Trace element characterisation of glass shards reveals the role of magmatic processes that are not readily apparent in the relatively homogeneous major element compositions. Multi-element diagrams show prominent negative Sr and Ti anomalies against primitive mantle likely caused by various degrees of plagioclase and titanomagnetite fractional crystallisation in shallow magma chambers. Relative Nb depletion, characteristic of arc volcanism, is moderate in CVZ tephras. HFSEs (e.g. Nb, Zr, Ti) and HREEs (e.g. Yb, Lu) remain immobile during slab fluid flux suggesting they are derived from the mantle wedge. LILE (e.g. Rb, Cs, Ba, Sr) and LREE (e.g. La, Ce) enrichments are consistent with slab fluid contribution. B/La and Li/Y ratios can be used as a proxy for the flux of subducting material to the mantle wedge, they suggest there is a strong influence from this component in the generation of CVZ arc magmas, potentially inducing melting. CVZ tephra show long-term coherent variability in trace element geochemistry. Post ~ 4 Ma tephras display a more consistent, less variable, chemical fingerprint that persists up to and across the CVZ/TVZ transition at ~ 2 Ma. Initiation of TVZ volcanism may have occurred earlier than is presently considered, or CVZ to TVZ volcanism may have occurred without significant changes in magma generation processes.</p>

scholarly journals TephraNZ: a major and trace element reference dataset for prominent Quaternary rhyolitic tephras in New Zealand and implications for correlation

2020 ◽  
Author(s):  
Jenni L. Hopkins ◽  
Janine E. Bidmead ◽  
David J. Lowe ◽  
Richard J. Wysoczanski ◽  
Bradley J. Pillans ◽  
...  
Keyword(s):  
New Zealand ◽  
Trace Element ◽  
Major Element ◽  
Chemical Compositions ◽  
Volcanic Centre ◽  
Reference Dataset ◽  
Future Studies ◽  
Glass Shard ◽  
Tephra Deposits ◽  
Glass Shards

Abstract. Although analyses of tephra-derived glass shards have been undertaken in New Zealand for nearly four decades (pioneered by Paul Froggatt), our study is the first to systematically develop a formal, comprehensive, open access, reference dataset of glass-shard compositions for New Zealand tephras. These data will provide an important reference tool for future studies to identify and correlate tephra deposits and for associated petrological and magma-related studies within New Zealand and beyond. Here we present the foundation dataset for TephraNZ, an open access reference dataset for selected tephra deposits in New Zealand. Prominent, rhyolitic, tephra deposits from the Quaternary were identified, with sample collection targeting original type sites or reference locations where the tephra's identification is unequivocally known based on independent dating or mineralogical techniques. Glass shards were extracted from the tephra deposits and major and trace element geochemical compositions were determined. We discuss in detail the data reduction process used to obtain the results and propose that future studies follow a similar protocol in order to gain comparable data. The dataset contains analyses of twenty-three proximal and twenty-seven distal tephra samples characterising 45 eruptive episodes ranging from Kaharoa (636 &amp;pm; 12 cal. yrs BP) to the Hikuroa Pumice member (2.0 &amp;pm; 0.6 Ma) from six or more caldera sources, most from the central Taupō Volcanic Zone. We report 1385 major element analyses obtained by electron microprobe (EMPA), and 590 trace element analyses obtained by laser ablation (LA)-ICP-MS, on individual glass shards. Using PCA, Euclidean similarity coefficients, and geochemical investigation, we show that chemical compositions of glass shards from individual eruptions are commonly distinguished by major elements, especially CaO, TiO2, K2O, FeOt (Na2O+ K2O and SiO2/K2O), but not always. For those tephras with similar glass major-element signatures, some can be distinguished using trace elements (e.g. HFSEs: Zr, Hf, Nb; LILE: Ba, Rb; REE: Eu, Tm, Dy, Y, Tb, Gd, Er, Ho, Yb, Sm), and trace element ratios (e.g. LILE / HFSE: Ba / Th, Ba / Zr, Rb / Zr; HFSE / HREE: Zr / Y, Zr / Yb, Hf / Y; LREE / HREE: La / Yb, Ce / Yb). Geochemistry alone cannot be used to distinguish between glass shards from the following tephra groups: Taupō (Unit Y in the post-Ōruanui eruption sequence of Taupō volcano) and Waimihia (Unit S); Poronui (Unit C) and Karapiti (Unit B); Rotorua and Rerewhakaaitu; and Kawakawa/Ōruanui, Okaia, and Unit L (of the Mangaone subgroup eruption sequence). Other characteristics can be used to separate and distinguish all of these otherwise-similar eruptives except Poronui and Karapiti. Bimodality caused by K2O variability is newly identified in Poihipi and Tahuna tephras. Using glass shard compositions, tephra sourced from Taupō Volcanic Centre (TVC) and Mangakino Volcanic Centre (MgVC) can be separated using bivariate plots of SiO2/K2O vs. Na2O+K2O. Glass shards from tephras derived from Kapenga Volcanic Centre, Rotorua Volcanic Centre, and Whakamaru Volcanic Centre have similar major- and trace-element chemical compositions to those from the MgVC, but can overlap with glass analyses from tephras from Taupō and Okataina volcanic centres. Specific trace elements and trace element ratios have lower variability than the heterogeneous major element and bimodal signatures, making them easier to geochemically fingerprint.

The Geochemistry of the Granitic Rocks of Halifax County, Nova Scotia

1974 ◽  
Vol 11 (5) ◽  
pp. 650-657 ◽  
Author(s):  
T. E. Smith
Keyword(s):  
Nova Scotia ◽  
Trace Element ◽  
Major Element ◽  
Biotite Granite ◽  
Granitic Rocks ◽  
Trace Element Chemistry ◽  
Quartz Monzonite ◽  
Lower Palaeozoic ◽  
Element Variation

Studies of part of a large batholith in southwest Nova Scotia show that granitic rocks of two different ages penetrate the Lower Palaeozoic metasediments of the Meguma Group. They are distinguished by their field relationships, mineralogy, and petrology from an older series, varying from biotite granodiorite through quartz monzonite to muscovite biotite granite, which is penetrated by younger large dikes, up to 1.5 km wide, of alaskite. Rb–Sr whole rock isochron ages show that the older series was emplaced approximately 415 m.y. ago and that the younger alaskite dikes were emplaced about 350 m.y. ago. Major and trace element chemistry shows that the older series of granitic rocks were formed by differentiation of a calc-alkali magma in situ. The younger dikes are all highly silicic, show limited major element variation, and have been affected by hydrothermal metasomatism.

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.

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