Geochemical and O-C-Sr-Nd Isotopic Constraints on the Petrogenetic Link between Aillikites and Carbonatites in the Tarim Large Igneous Province

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.

2021 ◽  
Vol 8 ◽  
Author(s):  
Nordine Bouden ◽  
Johan Villeneuve ◽  
Yves Marrocchi ◽  
Etienne Deloule ◽  
Evelyn Füri ◽  
...  

Secondary ion mass spectrometry (SIMS) is a powerful technique for in situ triple oxygen isotope measurements that has been used for more than 30 years. Since pioneering works performed on small-radius ion microprobes in the mid-80s, tremendous progress has been made in terms of analytical precision, spatial resolution and analysis duration. In this respect, the emergence in the mid-90s of the large-radius ion microprobe equipped with a multi-collector system (MC-SIMS) was a game changer. Further developments achieved on CAMECA MC-SIMS since then (e.g., stability of the electronics, enhanced transmission of secondary ions, automatic centering of the secondary ion beam, enhanced control of the magnetic field, 1012Ω resistor for the Faraday cup amplifiers) allow nowadays to routinely measure oxygen isotopic ratios (18O/16O and 17O/16O) in various matrices with a precision (internal error and reproducibility) better than 0.5‰ (2σ), a spatial resolution smaller than 10 µm and in a few minutes per analysis. This paper focuses on the application of the MC-SIMS technique to the in situ monitoring of mass-independent triple oxygen isotope variations.


Author(s):  
Miaohong He ◽  
Tianyu Chen ◽  
Xi Liu ◽  
Ya-Nan Yang ◽  
Xiaoping Xia ◽  
...  

Accurate oxygen isotopic analysis of aragonite by secondary ion mass spectrometry (SIMS) requires appropriate reference materials to calibrate systems for instrumental mass fractionation. Several hundred SIMS oxygen isotopic analyses were...


Author(s):  
C. Jung ◽  
S. Jung ◽  
E. Hellebrand ◽  
E. Hoffer

ABSTRACTTrace element abundances in garnet from a polyphase migmatite were measured by secondary ion mass spectrometry (SIMS) in order to identify some of the effective variables on the trace element distribution between garnet and melanosome or leucosome. In general, garnet is zoned with respect to REE, in which garnet cores are enriched by a factor of 2–3 relative to the rims. For an inclusion-rich garnet from the melanosome, equilibrium distribution following a simple Rayleigh fractionation is responsible for the decreasing concentrations in REE from core to rim. Inclusion-poor garnet from the same melanosome located in the vicinity of the leucosomes shows distinct enrichment and depletion patterns for REE from core to rim. These features suggest disequilibrium between garnet and the host rock which, in this case, could have been an in-situ derived melt. This would probably indicate a period of open-system behaviour at a time when the garnet, originally nucleated in the metamorphic environment reacted with the melt. In addition, non-gradual variation in trace element abundances between core and rim may suggest variable garnet growth rates. Inclusion-free garnet from the leucosome, interpreted to have crystallised in the presence of a melt, has a small core with high REE abundances and a broad rim with lower REE abundances. Here, crystal-liquid diffusion-controlled partitioning is a likely process to explain the trace element variation.


Minerals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1030
Author(s):  
Zhi Shang ◽  
Yongqing Chen

The Gejiu Anisian alkaline basalts (GAAB), distributed in the southern part of the Emeishan large igneous province (ELIP), are crucial to understand the tectonomagmatic activity during the Triassic. Geochronological, geochemical, and Sr-Nd-Pb isotopic analyses were systematically applied to explore the origin, petrogenesis, and tectonic setting of the GAAB, and how they relate to the ELIP. Zircon U-Pb dating set the eruption date at 244 Ma. Most of the samples belonged to alkaline basalts and had high TiO2 (2.14–3.23 wt.%) and MgO (4.43–19.58 wt.%) contents. Large ion lithophile elements (LILEs) were enriched relative to high field strength elements (HFSEs). The rare earth elements (REEs) and trace element signatures in the normalized diagrams were similar to oceanic island basalts (OIB) and Emeishan high-Ti basalts. These samples had consistent Sr-Nd isotope compositions: the initial 87Sr/86Sr values ranged from 0.7044 to 0.7048 and εNd(t) = 3.25–4.92. The Pb isotopes were more complex, the (206Pb/204Pb)t, (207Pb/204Pb)t, (208Pb/204Pb)t ratios were 17.493–18.197, 15.530–15.722, and 37.713–38.853, respectively. Our results indicate that the GAAB originated from the deeper enriched mantle with 5% to 15% partial melting of garnet lherzolite and a segregation depth of 2 to 4 GPa (60–120 km). During the formation of the GAAB, clinopyroxene and Ti-Fe oxides were fractionally crystallized with insignificant crustal contamination. The GAAB were formed in a extensional regime that was related to the Gejiu-Napo rift event in the Triassic.


2020 ◽  
Author(s):  
Feifei Jia ◽  
Jie Wang ◽  
Yanyan Zhang ◽  
Qun Luo ◽  
Luyu Qi ◽  
...  

<p></p><p><i>In situ</i> visualization of proteins of interest at single cell level is attractive in cell biology, molecular biology and biomedicine, which usually involves photon, electron or X-ray based imaging methods. Herein, we report an optics-free strategy that images a specific protein in single cells by time of flight-secondary ion mass spectrometry (ToF-SIMS) following genetic incorporation of fluorine-containing unnatural amino acids as a chemical tag into the protein via genetic code expansion technique. The method was developed and validated by imaging GFP in E. coli and human HeLa cancer cells, and then utilized to visualize the distribution of chemotaxis protein CheA in E. coli cells and the interaction between high mobility group box 1 protein and cisplatin damaged DNA in HeLa cells. The present work highlights the power of ToF-SIMS imaging combined with genetically encoded chemical tags for <i>in situ </i>visualization of proteins of interest as well as the interactions between proteins and drugs or drug damaged DNA in single cells.</p><p></p>


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