Mineral/melt partition coefficients of oceanic alkali basalts determined on natural samples using laser ablation-inductively coupled plasma-mass spectrometry (LAM-ICP-MS)

2000 ◽  
Vol 64 (1) ◽  
pp. 85-94 ◽  
Author(s):  
G. M. Thompson ◽  
J. Malpas
Keyword(s):  
Trace Elements ◽  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Partition Coefficients ◽  
Dominant Factor ◽  
Alkali Basalts ◽  
Compositional Evolution ◽  
Icp Ms ◽  
D Values ◽  
The Impact

AbstractIn order to limit the range of possible differentiation mechanisms and the impact of these processes on the trace element signatures of igneous suites, it is important to be able to predict or model the compositional evolution of the primary and/or parental magmas. Part of the problem in understanding these relationships in basalts from ocean islands is the paucity of reliable trace element mineral/melt partition coefficients, particularly for undersaturated magmas. Consequently, we have measured mineral/groundmass partition coefficients for Rb, Sr, Y, Zr, Nb, Hf, Ta, Th and REE, in situ, in clinopyroxene, Fe-Ti oxides and olivine in primitive basalts from Rarotonga, Cook Islands using LAM-ICP-MS.Analyses of these mafic rocks show high concentrations of most incompatible trace elements (e.g. Sr, Th, Y, REE, etc.) in pyroxenes relative to the other phases, suggesting that fractionation of pyroxenes was the dominant factor in the distribution of these trace elements during crystal fractionation. In such cases, the highly incompatible elements (D <0.01) are Ba, Cs and Nb. Elements that could also be classified as strongly incompatible (D <0.1) are Rb, Ta and Th. The remaining trace elements have bulk partition coefficient values that range from ∼.0.1 up to ∼.0.8 (Sr, Hf, Zr, Y and REE). Magnetites incorporate greater amounts of Nb and Ta than the titanaugites, and any significant fractionation of magnetite would have affected the bulk distribution of Nb and Ta. The LREE have lower Kd values than other REE, with the HREE having Kd values close to unity. Consequently, with the separation of titanaugite an overall enrichment of REE in the residual liquid with an increase in the La/Yb ratio is produced.

scholarly journals Trace Elements in Magnetite from the Pagoni Rachi Porphyry Prospect, NE Greece: Implications for Ore Genesis and Exploration

Minerals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 725 ◽  
Author(s):  
Constantinos Mavrogonatos ◽  
Panagiotis Voudouris ◽  
Jasper Berndt ◽  
Stephan Klemme ◽  
Federica Zaccarini ◽  
...  
Keyword(s):  
Trace Elements ◽  
Laser Ablation ◽  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Ore Deposits ◽  
Hydrothermal Conditions ◽  
Northern Greece ◽  
Icp Ms ◽  
Accessory Phase ◽  
Granodiorite Porphyry

Magnetite is a common accessory phase in various types of ore deposits. Its trace element content has proven to have critical implications regarding petrogenesis and as guides in the exploration for ore deposits in general. In this study we use LA-ICP-MS (laser ablation-inductively coupled plasma-mass spectrometry) analyses of trace elements to chemically characterize magnetite from the Pagoni Rachi Cu–Mo–Re–Au porphyry-style prospect, Thrace, northern Greece. Igneous magnetite mostly occurs as euhedral grains, which are commonly replaced by hematite in fresh to propylitic-altered granodiorite porphyry, whereas, hydrothermal magnetite forms narrow veinlets or is disseminated in sodic/potassic-calcic altered (albite + K-feldspar + actinolite + biotite + chlorite) granodiorite porphyry. Magnetite is commonly associated with chalcopyrite and pyrite and locally exhibits martitization. Laser ablation ICP-MS analyses of hydrothermal magnetite yielded elevated concentrations in several trace elements (e.g., V, Pb, W, Mo, Ta, Zn, Cu, and Nb) whereas Ti, Cr, Ni, and Sn display higher concentration in its magmatic counterpart. A noteworthy enrichment in Mo, Pb, and Zn is an unusual feature of hydrothermal magnetite from Pagoni Rachi. High Si, Al, and Ca values in a few analyses of hydrothermal magnetite imply the presence of submicroscopic or nano-inclusions (e.g., chlorite, and titanite). The trace element patterns of the hydrothermal magnetite and especially the decrease in its Ti content reflect an evolution from the magmatic towards the hydrothermal conditions under decreasing temperatures, which is consistent with findings from analogous porphyry-style deposits elsewhere.

scholarly journals Simultaneous Quantification of Forsterite Content and Minor–Trace Elements in Olivine by LA–ICP–MS and Geological Applications in Emeishan Large Igneous Province

Minerals ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 634
Author(s):  
Shitou Wu ◽  
Yadong Wu ◽  
Yueheng Yang ◽  
Hao Wang ◽  
Chao Huang ◽  
...  
Keyword(s):  
Trace Elements ◽  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Large Igneous Province ◽  
Emeishan Large Igneous Province ◽  
Inductively Coupled ◽  
Minor Elements ◽  
Icp Ms ◽  
Igneous Province ◽  
Peridotitic Mantle

Olivine forsterite contents [Fo = 100 × Mg/(Mg + Fe) in mol%] and minor–trace element concentrations can aid our understanding of the Earth’s mantle. Traditionally, these data are obtained by electron probe microanalysis for Fo contents and minor elements, and then by laser ablation–inductively coupled plasma–mass spectrometry (LA–ICP–MS) for trace elements. In this study, we demonstrate that LA–ICP–MS, with a simplified 100% quantification approach, allows the calculation of Fo contents simultaneously with minor–trace elements. The approach proceeds as follows: (1) calculation of Fo contents from measured Fe/Mg ratios; (2) according to the olivine stoichiometric formula [(Mg, Fe)2SiO4] and known Fo contents, contents of Mg, Fe and Si can be computed, which are used as internal standards for minor–trace element quantification. The Fo content of the MongOLSh 11-2 olivine reference material is 89.55 ± 0.15 (2 s; N = 120), which agrees with the recommended values of 89.53 ± 0.05 (2 s). For minor–trace elements, the results matched well with the recommended values, apart from P and Zn data. This technique was applied to olivine phenocrysts in the Lijiang picrites from the Emeishan large igneous province. The olivine compositions suggest that the Lijiang picrites have a peridotitic mantle source.

Paleoredox conditions, hydrothermal history, and target vectoring in the Macmillan Pass base-metal district, Yukon, Canada: 2 – Pyrite paragenesis and mineral chemistry

2021 ◽  
Vol 59 (5) ◽  
pp. 1233-1259
Author(s):  
Claire Leighton ◽  
Daniel Layton-Matthews ◽  
Jan M. Peter ◽  
Michael G. Gadd ◽  
Alexandre Voinot ◽  
...  
Keyword(s):  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Mineral Chemistry ◽  
Hydrothermal Activity ◽  
Unconsolidated Sediments ◽  
Lateral Migration ◽  
Sulfide Mineralization ◽  
Ambient Seawater ◽  
Clastic Sediment ◽  
Icp Ms

ABSTRACT The MacMillan Pass district in Yukon, Canada, hosts the Tom and Jason clastic sediment-hosted Zn-Pb-Ag-(Ba) deposits. Pyrite-bearing drill core samples were collected from seven drill holes that intersected sulfide mineralization and time-stratigraphically equivalent rocks at varied spatial distances extending up to 3 km away from the deposits to assess the relative timing of pyrite mineralization and the chemistry of pyrite paragenesis. There are four pyrite morphologies: framboids and polyframboids (Py1), subhedral to euhedral inclusion-free crystals (Py2a), silicate inclusion-bearing nodules with serrated edges (Py2b), and euhedral idiomorphic overgrowths on preexisting pyrite morphologies (Py3). These morphological varieties correspond in time from syngenetic to earliest diagenetic growth (Py1), early to late diagenetic growth (Py2a, Py2b), and metamorphic crystallization and/or recrystallization of previous textural varieties (Py3). A representative subset of pyrite grains was analyzed for trace element contents and distributions by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). Analyses by LA-ICP-MS reveal that each textural variety of pyrite has a distinct trace element composition that also varies depending on stratigraphic unit. A suite of clastic sediment-hosted sulfide mineralization-related elements was incorporated into Py2 within sulfide mineralized units at greater abundances than that in unmineralized units (e.g., Zn, As, Pb, Tl, Bi). Lead abundances and Pb/Se and As/Mo values in pyrite are the most robust vectoring tools documented. The timing for clastic sediment-hosted Zn-Pb mineralization was syn and/or post late diagenesis (Py2b). A Ba-enriched horizon was identified in rocks and this is interpreted to be the distal time-stratigraphic equivalent unit to Zn-Pb mineralization. The Ba-enriched horizon contains Py2 with anomalous metal (Tl, Co, Mn, Cd, Zn, Sb) contents and abundant macroscopic baryte, and it is interpreted to represent the distal expression of sulfide mineralization-forming hydrothermal activity. Four genetic models for mineralization are reviewed; however, the only model that is consistent with our whole rock and pyrite geochemistry involves venting of buoyant hydrothermal fluid, mixing with ambient seawater, and remaining or sinking into unconsolidated sediments, with lateral migration up to 2–3 km from the vent source.

scholarly journals Using trace elements to identify the geographic origin of migratory bats

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e10082
Author(s):  
Jamin G. Wieringa ◽  
Juliet Nagel ◽  
David M. Nelson ◽  
Bryan C. Carstens ◽  
H. Lisle Gibbs
Keyword(s):  
Trace Elements ◽  
Wind Energy ◽  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Geographic Origin ◽  
Lasiurus Borealis ◽  
Inductively Coupled ◽  
Plasma Mass Spectrometry ◽  
Trace Element Profiles ◽  
Geographic Sources

The expansion of the wind energy industry has had benefits in terms of increased renewable energy production but has also led to increased mortality of migratory bats due to interactions with wind turbines. A key question that could guide bat-related management activities is identifying the geographic origin of bats killed at wind-energy facilities. Generating this information requires developing new methods for identifying the geographic sources of individual bats. Here we explore the viability of assigning geographic origin using trace element analyses of fur to infer the summer molting location of eastern red bats (Lasiurus borealis). Our approach is based on the idea that the concentration of trace elements in bat fur is related through the food chain to the amount of trace elements present in the soil, which varies across large geographic scales. Specifically, we used inductively coupled plasma–mass spectrometry to determine the concentration of fourteen trace elements in fur of 126 known-origin eastern red bats to generate a basemap for assignment throughout the range of this species in eastern North America. We then compared this map to publicly available soil trace element concentrations for the U.S. and Canada, used a probabilistic framework to generate likelihood-of-origin maps for each bat, and assessed how well trace element profiles predicted the origins of these individuals. Overall, our results suggest that trace elements allow successful assignment of individual bats 80% of the time while reducing probable locations in half. Our study supports the use of trace elements to identify the geographic origin of eastern red and perhaps other migratory bats, particularly when combined with data from other biomarkers such as genetic and stable isotope data.

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