scholarly journals Co-magmatic sulfides and sulfates in the Udachnaya-East pipe (Siberia): sulfur speciation and isotopic composition in kimberlites and their mantle sources

2017 ◽  
Vol 455 ◽  
pp. 315-330 ◽  
Author(s):  
Yumi Kitayama ◽  
Emilie Thomassot ◽  
Αlbert Galy ◽  
Alexander Golovin ◽  
Andrey Korsakov ◽  
...  

2020 ◽  
Author(s):  
Andrea Giuliani ◽  
Janne M. Koornneef ◽  
Peter Barry ◽  
Patrizia Will ◽  
Henner Busemann ◽  
...  

<p>Kimberlites are the deepest melts that reach Earth’s surface and, therefore, can provide unique insights into the composition and evolution of the convective mantle through time. Application of isotope geochemistry to trace the composition of kimberlite sources has thus far been hindered by the ubiquitous alteration and incorporation of xenocrystic material in kimberlite rocks. Bulk-kimberlite analyses are typically considered reliable for Nd and Hf isotopes due to their overwhelmingly higher concentrations in kimberlite melts compared to common mantle and crustal contaminants. Conversely, Sr and Pb isotope compositions of bulk kimberlite samples are seldom considered representative of their parental melts thus requiring analysis of robust magmatic phases, primarily perovskite. Addressing the primary (i.e. magmatic) isotopic composition of volatile elements, such as N and noble gases, requires analyses of volatile-rich phases, and fluid inclusions in olivine represent a typical primary target in mantle-derived magmas. However, fluid inclusions in kimberlitic olivine are dominantly secondary in origin. Secondary inclusions can form at any time after crystallisation of their mineral host, which requires assessment of the origin of trapped fluids (i.e. pristine magmatic fluids, crustal fluids of external derivation, or combination thereof) before their isotopic composition can be used to make inferences about kimberlite mantle sources.</p><p>Here we present trace-element and Sr-Nd-Pb-He-N isotopic compositions of multiple olivine aliquots representing two different magmatic units of the ~88 Ma Wesselton kimberlite (Kimberley, South Africa). The Sr and Nd isotopic composition of olivine analysed by isotope-dilution (ID) TIMS are within the narrow range of perovskite <sup>87</sup>Sr/<sup>86</sup>Sr (0.7043-0.7046) and whole-rock <sup>143</sup>Nd/<sup>144</sup>Nd (eNd<sub>i</sub> = 0.4–2.2) for the Kimberley kimberlites. These results indicate that the secondary fluid inclusions, which dominate the incompatible trace-element budget of olivine separates, have a pristine magmatic origin devoid of crustal contribution.</p><p>Helium isotope compositions were measured by laser heating of 1.6 to 9.8 mg of olivine using an ultrahigh-sensitivity compressor-source noble gas mass spectrometer. <sup>3</sup>He/<sup>4</sup>He ratios are between 1.6 R<sub>A</sub> and 3.7 R<sub>A</sub> (where R<sub>A</sub> indicates the atmospheric <sup>3</sup>He/<sup>4</sup>He ratio), values more radiogenic than MORBs but comparable to HIMU OIBs. These results indicate a high time-integrated (U+Th)/He ratio in the source of the Kimberley kimberlites, which is consistent with the moderately high (i.e. HIMU-like) time-integrated U/Pb ratio implied by elevated initial <sup>206</sup>Pb/<sup>204</sup>Pb in Wesselton olivine (19.1-19.5), Kimberley kimberlites (up to 19.9) and megacrysts in southern African Cretaceous kimberlites (up to 20.5). The combination of low <sup>3</sup>He/<sup>4</sup>He, moderately radiogenic <sup>87</sup>Sr/<sup>86</sup>Sr, and negative d<sup>34</sup>S values (-2.6‰ to -5.7‰) require a contribution from subducted recycled material in the source of the Kimberley kimberlites. Conversely, a preliminary N isotope analysis of Wesselton olivine by in-vacuo crushing using a noble gas mass spectrometer returned a mantle-like d<sup>15</sup>N of -2.9‰, which might suggest limited recycling of surface N (d<sup>15</sup>N >0‰) in the source of these kimberlites. We conclude that the combination of Sr-Nd-Pb and He-N isotope tracing of fluid inclusions in olivine can provide a robust new approach to address the composition of kimberlite sources and, therefore, the evolution of the deep mantle through time.</p>


2007 ◽  
Vol 254 (1-2) ◽  
pp. 77-89 ◽  
Author(s):  
Ralf Halama ◽  
William F. McDonough ◽  
Roberta L. Rudnick ◽  
Jörg Keller ◽  
Jurgis Klaudius

1997 ◽  
Vol 34 (4) ◽  
pp. 489-503 ◽  
Author(s):  
Steven B. Shirey

Picrites and tholeiites from the Mamainse Point Formation, a 5.3 km thick section of Keweenawan (1100 Ma) volcanic and sedimentary fill on the eastern flank of the central portion of the Midcontinent rift system, contain a nearly continuous record of rift magmatic activity. Picrites occur primarily in the lowermost two units of the formation. In this study, they are compared to rarely exposed, slightly older Keweenawan basalts from the North Shore Volcanic Group and the Powder Mill Group to constrain mantle source compositions during early phases of rift magmatic activity. The most primitive picrites analyzed have low Re content (0.069–0.18 ppb), high Os content (0.8–2.1 ppb), and low 187Re/188Os (0.28–1.18). A Re–Os isochron with an age of 1128 ± 54 Ma and an initial 187Os/188Os of 0.1267 ± 0.0013 (γOs = +5.7) was obtained from a 24-point isochron on all but two analyzed samples. The Re–Os data, regressed separately for the older basalts, and the groups 1 and 2 samples from the Mamainse Point Formation, have barely resolvable initial 187Os/188Os that decrease up-stratigraphy from initial γOs(1100) of +12.2 to +6.2 and +4.2, respectively, and couple with changes in initial Nd isotopic composition. These data can be explained by mixing of melts of an enriched mantle plume and unradiogenic continental lithospheric mantle. A radiogenic initial Os isotopic composition (γOs of +8 or higher) for the Keweenawan plume marks the first known appearance of demonstrably radiogenic plume-derived magmas on Earth. Plume-derived magmas with radiogenic Os signatures are more common later. The radiogenic Os signatures of Keweenawan plume magmas may mark the appearance of melts derived from mantle containing recycled slab components from late Archean subduction.


2015 ◽  
Vol 79 (2) ◽  
pp. 219-241 ◽  
Author(s):  
K. Bell ◽  
A. N. Zaitsev ◽  
J. Spratt ◽  
S. Fröjdö ◽  
A. S. Rukhlov

AbstractGalena from four REE-rich (Khibina, Sallanlatvi, Seblyavr, Vuoriyarvi) and REE-poor (Kovdor) carbonatites, as well as hydrothermal veins (Khibina) all from the Devonian Kola Alkaline Province of northwestern Russia was analysed for trace elements and Pb and S isotope compositions. Microprobe analyses show that the only detectable elements in galena are Bi and Ag and these vary from not detectable to 2.23 and not detectable to 0.43 wt.% respectively. Three distinct galena groups can be recognized using Bi and Ag contents, which differ from groupings based on Pb isotope data. The Pb isotope ratios show significant spread with 206Pb/204Pb ratios (16.79 to 18.99), 207Pb/204Pb (15.22 to 15.58) and 208Pb/204Pb ratios (36.75 to 38.62). A near-linear array in a 207Pb/204Pb vs.206Pb/204Pb ratio diagram is consistent with mixing between distinct mantle sources, one of which formed during a major differentiation event in the late Archaean or earlier. The S isotopic composition (δ34S) of galena from carbonatites is significantly lighter (–6.7 to –10.3% Canyon Diablo Troilite (CDT) from REE-rich Khibina, Seblyavr and Vuoriyarvi carbonatites, and – 3.2% CDT from REE-poor Kovdor carbonatites) than the mantle value of 0%. Although there is no correlation between S and any of the Pb isotope ratios, Bi and Ag abundances correlate negatively with δ34S values. The variations in the isotopic composition of Pb are attributed to partial melting of an isotopically heterogeneous mantle source, while those of δ34S (together with Bi and Ag abundances) are considered to be process driven. Although variation in Pb isotope values between complexes might reflect different degrees of interaction between carbonatitic melts and continental crust or metasomatized lithosphere, the published noble gas and C, O, Sr, Nd and Hf isotopic data suggest that the variable Pb isotope ratios are best attributed to isotopic differences preserved within a sub-lithospheric mantle source. Different Pb isotopic compositions of galena from the same complex are consistent with a model of magma replenishment by carbonatitic melts/fluids each marked by quite different Pb isotopic compositions.


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