The corrosion of basaltic dykes in evaporites: Ar–Sr–Nd isotope and rare earth elements evidence

1999 ◽  
Vol 153 (1-4) ◽  
pp. 259-279 ◽  
Author(s):  
Marc Steinmann ◽  
Peter Stille ◽  
Walter Bernotat ◽  
Bernhard Knipping
2018 ◽  
Vol 484 ◽  
pp. 120-135 ◽  
Author(s):  
Emilie Janots ◽  
Håkon Austrheim ◽  
Carl Spandler ◽  
Johannes Hammerli ◽  
Claudia A. Trepmann ◽  
...  

Mineralogia ◽  
2007 ◽  
Vol 38 (1) ◽  
pp. 29-45 ◽  
Author(s):  
Elena Balaganskaya ◽  
Hilary Downes ◽  
Daniel Demaiffe

Ree and Sr-Nd Isotope Compositions of Clinopyroxenites, Phoscorites and Carbonatites of the Seblyavr Massif, Kola Peninsula, RussiaClinopyroxenites, phoscorites and carbonatites from the Devonian Seblyavr intrusion (Kola Peninsula, Russia) have petrographic characteristics indicating that they are accumulative in origin. Their geochemical (major and rare earth elements) compositions can be accounted for by mixtures of their major rock-forming minerals and accessory phases, i.e. they reflect the record of mineral accumulation. All of the analysed Seblyavr rocks are strongly LREE-enriched with (La/Yb)N mostly ranging from 38 to 189. However, a dolomite carbonatite with hydrothermal LREE-Sr mineralization has an extreme (La/Yb)N value of 1659. Such late-stage dolomite carbonatites were formed by hydrothermal (rather than magmatic) processes. Whole-rock samples of representative magmatic lithologies from Seblyavr have initial 87Sr/86Sr and εNd that fall in a very narrow range from 0.7031 to 0.7033 and +4.9 to +5.9, respectively. We therefore conclude that clinopyroxenites, phoscorites and carbonatites were formed by differentiation and crystallization of a single batch of melt. The parental melt was derived from a depleted upper mantle source that had been meta-somatised prior to melting.


2013 ◽  
Vol 151 (4) ◽  
pp. 573-590 ◽  
Author(s):  
PETER DAHLIN ◽  
ÅKE JOHANSSON ◽  
ULF B. ANDERSSON

AbstractThe geochemical and isotopic characteristics of metamorphosed Svecofennian mafic dykes from the Dannemora area in the NE part of the Bergslagen region in central Sweden were investigated and compared to mafic intrusive rocks in their vicinity. The dykes, with an inferred age of c. 1860–1870 Ma, are calc-alkaline, sub-alkaline and basaltic in composition and have a mixed subduction and within-plate geochemical affinity. They are the result of mixing of at least three mantle source components with similar basaltic major element composition, but different concentrations of incompatible trace elements. Magma M1 is strongly enriched both in Rare Earth Elements (REE) and High-Field-Strength Elements (HFSE); magma M2 is highly enriched in Large-Ion Lithophile Elements (LILE, except Sr) with only moderate enrichment in HFSE and REE (particularly low in Heavy Rare Earth Elements); and magma M3 is enriched in Sr and has a flat REE profile. Magma M3 also has a somewhat more positive (depleted) initial εNd value of +1.8, compared to +0.4 to +0.5 for magmas M1 and M2. The magma evolution was controlled by a mixture of fractionation (mainly affecting the compatible elements) and mixing, best seen in the incompatible element concentrations and the Nd isotope data. The basaltic overall composition indicates little or no wholesale contamination by upper continental crust, but the dykes have undergone later metasomatic changes mainly affecting the alkali elements.


Minerals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1141
Author(s):  
Tiancheng Zhou ◽  
Xuefa Shi ◽  
Mu Huang ◽  
Miao Yu ◽  
Dongjie Bi ◽  
...  

Rare earth elements (REEs) and yttrium (Y), together known as REY, are extremely enriched in deep-sea pelagic sediments, attracting much attention as a promising new REY resource. To understand the influence of hydrothermal processes on the enrichment of REY in deep-sea sediments from the eastern South Pacific Ocean, we conducted detailed lithological, bulk sediment geochemical, and in situ mineral geochemical analyses on gravity core sample S021GC17 from the Yupanqui Basin of eastern South Pacific. The REY-rich muds of S021GC17 are dark-brown to black zeolitic clays with REY contents (ΣREY) ranging from 1057 to 1882 ppm (average 1329 ppm). The REY-rich muds display heavy rare earth elements (HREE) enriched patterns, with obvious depletions in Ce, and positive anomalies of Eu in Post-Archean Australian Shale (PAAS)-normalized REE diagrams. In contrast, the muds of S021GC17 show light rare earth elements (LREE) enriched patterns and positive anomalies of Ce and Eu in the seawater-normalized REE diagrams. Total REY abundances in the core show positive correlations with CaO, P2O5, Fe2O3, and MnO concentrations. In situ analyses of trace element contents by laser ablation-inductively coupled plasma–mass spectrometry (LA-ICP-MS) demonstrate that bioapatite fossils contain high REY concentrations (998 to 22,497 ppm, average 9123 ppm), indicating that they are the primary carriers of REY. The in situ Nd isotope values of bioapatites are higher than the average values of seawater in Pacific Ocean. Fe–Mn micronodules are divided into hydrogenetic and diagenetic types, which have average REY concentrations of 1586 and 567 ppm, respectively. The high contents of Fe-Mn-Ba-Co-Mo, the positive correlations between ΣREY and Fe-Mn, the ratios of Fe/Ti and Al/(Al + Fe + Mn), and the LREE-enriched patterns in the REY-rich muds, combined with high Nd isotope values shown by bioapatite fossils, strongly indicate that the hydrothermal fluids have played an important role in the formation of the REY-rich sediments in the eastern South Pacific Ocean.


1962 ◽  
Vol 18 (4) ◽  
pp. 1127-1153
Author(s):  
V FASSEL ◽  
R CURRY ◽  
R KNISELEY

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