Iron isotope fractionation during sulfide liquid evolution in Cu–PGE mineralization of the Eastern Gabbro, Coldwell Complex, Canada

2021 ◽  
pp. 120282
Author(s):  
Matthew J. Brzozowski ◽  
David J. Good ◽  
Changzhi Wu ◽  
Weiqiang Li
Minerals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 464
Author(s):  
Peiyao Wang ◽  
Yaoling Niu ◽  
Pu Sun ◽  
Xiaohong Wang ◽  
Pengyuan Guo ◽  
...  

Many studies have shown that the average iron (Fe) isotope compositions of mantle-derived rocks, mantle peridotite and model mantle are close to those of chondrites. Therefore, it is considered that chondrite values represent the bulk Earth Fe isotope composition. However, this is a brave assumption because nearly 90% of Fe of the Earth is in the core, where its Fe isotope composition is unknown, but it is required to construct bulk Earth Fe isotope composition. We approach the problem by assuming that the Earth’s core separation can be approximated in terms of the Sudbury-type Ni-Cu sulfide mineralization, where sulfide-saturated mafic magmas segregate into immiscible sulfide liquid and silicate liquid. Their density/buoyancy controlled stratification and solidification produced net-textured ores above massive ores and below disseminated ores. The coexisting sulfide minerals (pyrrhotite (Po) > pentlandite (Pn) > chalcopyrite (Cp)) and silicate minerals (olivine (Ol) > orthopyroxene (Opx) > clinopyroxene (Cpx)) are expected to hold messages on Fe isotope fractionation between the two liquids before their solidification. We studied the net-textured ores of the Sudbury-type Jinchuan Ni-Cu sulfide deposit. The sulfide minerals show varying δ56Fe values (−1.37–−0.74‰ (Po) < 0.09–0.56‰ (Cp) < 0.53–1.05‰ (Pn)), but silicate minerals (Ol, Opx, and Cpx) have δ56Fe values close to chondrites (δ56Fe = −0.01 ± 0.01‰). The heavy δ56Fe value (0.52–0.60‰) of serpentines may reflect Fe isotopes exchange with the coexisting pyrrhotite with light δ56Fe. We obtained an equilibrium fractionation factor of Δ56Fesilicate-sulfide ≈ 0.51‰ between reconstructed silicate liquid (δ56Fe ≈ 0.21‰) and sulfide liquid (δ56Fe ≈ −0.30‰), or Δ56Fesilicate-sulfide ≈ 0.36‰ between the weighted mean bulk-silicate minerals (δ56Fe[0.70ol,0.25opx,0.05cpx] = 0.06‰) with weighted mean bulk-sulfide minerals (δ56Fe ≈ −0.30‰). Our study indicates that significant Fe isotope fractionation does take place between silicate and sulfide liquids during the Sudbury-type sulfide mineralization. We hypothesize that significant iron isotope fractionation must have taken place during core–mantle segregation, and the bulk Earth may have lighter Fe isotope composition than chondrites although Fe isotope analysis on experimental sulfide-silicate liquids produced under the varying mantle depth conditions is needed to test our results. We advocate the importance of further research on the subject. Given the close Fe-Ni association in the magmatic mineralization and the majority of the Earth’s Ni is also in the core, we infer that Ni isotope fractionation must also have taken place during the core separation that needs attention.


2019 ◽  
Vol 245 ◽  
pp. 59-78 ◽  
Author(s):  
Bradley J. Peters ◽  
Anat Shahar ◽  
Richard W. Carlson ◽  
James M.D. Day ◽  
Timothy D. Mock

2010 ◽  
Vol 74 (10) ◽  
pp. 2826-2842 ◽  
Author(s):  
A. Kappler ◽  
C.M. Johnson ◽  
H.A. Crosby ◽  
B.L. Beard ◽  
D.K. Newman

2020 ◽  
Vol 55 (8) ◽  
pp. 1515-1534
Author(s):  
M. Moilanen ◽  
E. Hanski ◽  
J. Konnunaho ◽  
T. Törmänen ◽  
S.-H. Yang ◽  
...  

Abstract Using electron probe microanalyzer (EPMA) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), we analyzed major and trace element compositions of iron oxides from Ni-Cu-PGE sulfide deposits hosted by mafic-ultramafic rocks in northern Fennoscandia, mostly focusing on Finland. The main research targets were the Archean Ruossakero Ni-(Cu) deposit; Tulppio dunite and related Ni-PGE mineralization; Hietaharju, Vaara, and Tainiovaara Ni-(Cu-PGE) deposits; and Paleoproterozoic Lomalampi PGE-(Ni-Cu) deposit. In addition, some reference samples from the Pechenga (Russia), Jinchuan (China), and Kevitsa (Finland) Ni-Cu-PGE sulfide deposits, and a barren komatiite sequence in the Kovero area (Finland) were studied. Magnetite and Cr-magnetite show a wide range of trace element compositions as a result of the variation of silicate and sulfide melt compositions and their post-magmatic modification history. Most importantly, the Ni content in oxide shows a positive correlation with the Ni tenor of the sulfide phase in equilibrium with magnetite, regardless of whether the sulfide assemblage is magmatic or post-magmatic in origin. The massive sulfide samples contain an oxide phase varying in composition from Cr-magnetite to magnetite, indicating that Cr-magnetite can crystallize directly from sulfide liquid. The Mg concentration of magnetites in massive sulfide samples is lowest among the samples analyzed, and this can be regarded as a diagnostic feature of an oxide phase crystallized together with primitive Fe-rich MSS (monosulfide solid solution). Our results show that magnetite geochemistry, plotted in appropriate discrimination diagrams, together with petrographical observations could be used as an indicator of potential Ni-(Cu-PGE) mineralization.


2015 ◽  
Vol 400 ◽  
pp. 24-33 ◽  
Author(s):  
Daniel S. Mulholland ◽  
Franck Poitrasson ◽  
Liudmila S. Shirokova ◽  
Aridane G. González ◽  
Oleg S. Pokrovsky ◽  
...  

2018 ◽  
Vol 222 ◽  
pp. 671-684 ◽  
Author(s):  
Hongjie Wu ◽  
Yongsheng He ◽  
Fang-Zhen Teng ◽  
Shan Ke ◽  
Zhenhui Hou ◽  
...  

2011 ◽  
Vol 308 (3-4) ◽  
pp. 317-324 ◽  
Author(s):  
Fang-Zhen Teng ◽  
Nicolas Dauphas ◽  
Rosalind T. Helz ◽  
Shan Gao ◽  
Shichun Huang

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