In situ trace element and Sm-Nd isotope analysis of accessory minerals in an Eoarchean tonalitic gneiss from Greenland: Implications for Hf and Nd isotope decoupling in Earth's ancient rocks

2019 ◽  
Vol 524 ◽  
pp. 394-405 ◽  
Author(s):  
Johannes Hammerli ◽  
Anthony I.S. Kemp ◽  
Martin J. Whitehouse
2019 ◽  
Vol 43 (4) ◽  
pp. 543-565 ◽  
Author(s):  
Yue‐Heng Yang ◽  
Fu‐Yuan Wu ◽  
Qiu‐Li Li ◽  
Yamirka Rojas‐Agramonte ◽  
Jin‐Hui Yang ◽  
...  
Keyword(s):  

2020 ◽  
Author(s):  
Johannes Hammerli

<p>The long-lived radiogenic isotope systems Lu-Hf and Sm-Nd have been widely used by geochemists to study magma sources and crustal residential times of (igneous) rocks in order to understand how early crust formed and to model the production rate and volume of continental crust on global and regional-scales during the last ~4.4 Ga. However, while throughout most of Earth’s history Nd and Hf isotope signatures in terrestrial rocks are well correlated due to their very similar geochemical behavior, some of Earth’s oldest rocks show an apparent inconsistency in their Nd and Hf isotope signatures. While Hf isotopes in early Archean rocks are generally (near) chondritic, Nd isotope signatures can be distinctly super- or sub-chondritic. The super-chondritic Nd isotope values in Eoarchean samples would suggest that these rocks are derived from a mantle reservoir depleted by prior crust extraction. The chondritic Hf isotope values, on the other hand, support a mantle source from which no significant volume of crust had been extracted. While a range of different processes, some of them speculative, might explain this Hf-Nd isotope paradox, recent research [1, 2] has shown that relatively simple, post-magmatic, open-system processes can explain decoupling of the typically correlative Hf-Nd isotope signatures. This talk will focus on the importance of identifying Nd-bearing accessory minerals in (Archean) rocks to understand how the Sm-Nd isotope system is controlled and how in situ isotope and trace element analyses by LA-(MC)-ICP-MS in combination with detailed petrographic observations help to understand when and via which processes the two isotope systems become decoupled. Reconstructing the isotopic evolution of the different isotope systems since formation of the protoliths has important implications for our understanding of early crust formation and questions some of the proposed current models for early crust extraction from the mantle.</p><p> </p><p>[1] Hammerli et al. (2019) Chem. Geol 2; [2] Fisher et al. (2020) EPSL</p>


2006 ◽  
Vol 70 (18) ◽  
pp. A479 ◽  
Author(s):  
N.J. Pearson ◽  
S.Y. O’Reilly ◽  
W.L. Griffin ◽  
O. Alard ◽  
E. Belousova

2009 ◽  
Vol 260 (1-2) ◽  
pp. 73-86 ◽  
Author(s):  
Courtney J. Gregory ◽  
Christopher R.M. McFarlane ◽  
Jörg Hermann ◽  
Daniela Rubatto

2022 ◽  
Author(s):  
Chao Wang ◽  
et al.

Text S1: Analytical methods. Figure S1: Zr versus selected element variation diagrams to highlight the effects of alteration and metamorphism for the basalts from Langjiexue area. Figure S2: (A) Ti/Y vs. TiO2, and (B) Ti/Y vs. MgO diagrams for the basalt samples from the Langjiexue in Tethyan Himalaya. Table S1: Representative Permian-Triassic magmatic events along the Tethyan Himalaya. Table S2: Zircon LA-ICP-MS U-Pb in-situ analyzing results for zircons from the Langjiexue basalts. Table S3: Whole-rock major, trace element and Sr-Nd isotope data of Langjiexue basalts.


Author(s):  
Changhong Wang ◽  
Zhaochong Zhang ◽  
Andrea Giuliani ◽  
Zhiguo Cheng ◽  
Bingxiang Liu ◽  
...  

Abstract Aillikites are carbonate-rich ultramafic lamprophyres often associated with carbonatites. Despite their common field relationships, the petrogenetic links, if any, between aillikites and carbonatites remain controversial. To address this question, this study reports the results of a detailed geochemical and isotopic examination of the Permian Wajilitag aillikites in the northwestern Tarim large igneous province, including bulk-rock major-, trace-element and Sr-Nd isotope compositions, olivine major- and trace-element and (in-situ secondary ion mass spectrometry) oxygen isotope compositions, oxygen isotope data for clinopyroxene separates, and bulk-carbonate C-O isotopic analyses. Olivine in the aillikites occurs in two textural types: (i) microcrysts, 0.3-5 mm; and (ii) macrocrysts, 0.5-2.5 cm. The microcrysts exhibit well-defined linear correlations between Fo (79-89), minor and trace elements (e.g., Ni = 1304-3764 μg/g and Mn = 1363-3042 μg/g). In contrast, the olivine macrocrysts show low Fo79-81, Ni (5.3-442 μg/g) and Ca (477-1018 μg/g) and very high Mn (3418-5123 μg/g) contents, and are displaced from the compositional trend of the microcrysts. The microcrysts are phenocrysts crystallized from the host aillikite magmas. Conversely, the lack of mantle-derived xenoliths in these aillikites suggests that the macrocrysts probably represent cognate crystals (i.e., antecrysts) that formed from earlier, evolved aillikite melts. Olivine phenocrysts in the more primitive aillikite dykes (Dyke 1) have relatively higher Fo82-89 and mantle-like oxygen isotope values, whereas those in the more evolved dykes (Dyke 2 and 3) exhibit lower Fo79-86 and oxygen isotope values that trend toward lower than mantle δ18O values. The decreasing δ13C values of carbonate from Dyke 1 through to Dyke 2 and 3, coupled with the indistinguishable Sr-Nd isotopes of these dykes, suggest that the low δ18O values of olivine phenocrysts in Dyke 2 and 3 resulted from carbonate melt/fluid exsolution from a common progenitor melt. These lines of evidence combined with the overlapping emplacement ages and Sr-Nd isotope compositions of the aillikites and carbonatites in this area suggest that these exsolved carbonate melts probably contributed to the formation of the Tarim carbonatites thus supporting a close petrogenetic relationship between aillikites and carbonatites.


2008 ◽  
Vol 254 (3-4) ◽  
pp. 197-215 ◽  
Author(s):  
Michael J. Jercinovic ◽  
Michael L. Williams ◽  
Edward D. Lane

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