• MakaleAçık Erişim2022Scopus SJRQ1
    Geochemical, isotopic and U-Pb geochronological investigation of the late Cretaceous Karaçayır carbonatite (Sivas, Turkey): Insights into mantle sources within a post-collisional tectonic setting

    Çimen, Okay; Ağrılı, Haşim; Kuebler, Corinne; Simonetti, Antonio; Corcoran, Loretta; Simonetti, Stefanie; Çolak, Turgut; İnal, Sedat; Dönmez, Cahit

    The Karaçayır carbonatite is located within the northeastern edge of the Central Anatolian Crystalline Complex, and represents one of the significant rare earth element (REE) mineralizations in Turkey. The carbonatite intrudes the associated syenite as dikes and veins, and is mainly composed of medium- to coarse-grained calcite, and lesser amounts of apatite, mica, amphibole, pyroxene, and magnetite. This study reports new and combined geochemical, radiogenic (Sr, Pb), stable (O and C), and for the first time B and Nd isotopic ratios and in-situ U-Pb age data from the Karaçayır carbonatite. The carbonate separates from the Karaçayır carbonatite are characterized by high Ba (30 to 484 ppm), Sr (613 to 9106 ppm) and total rare earth element (TREE) concentrations (172 to 2892 ppm), which are consistent with geochemical signatures for mantle-derived carbonate melts. The combined δ18OV-SMOW (+10.7 to +19.0 ‰), δ13CV-PDB (−2.9 to +1.8 ‰) and δ11B (−13.9 to −2.9 ‰) data for a majority of the carbonate separates investigated here in contrast indicate that they are the result of open system behavior involving contamination by the country rock (marble), and/or sub-solidus, low temperature alteration. Based on the combined stable and radiogenic isotopic signatures for the least altered/contaminated samples, the carbonatite magma at Karaçayır most likely represents a low-degree partial melt of an isotopically heterogeneous (metasomatized) mantle source containing EM (enriched mantle)-like components and recycled crustal carbon; the latter finding is consistent with those recorded for young (<300 Ma old) carbonatites worldwide. A weighted mean 206Pb/238U age of 69.3 ± 1.7 Ma is obtained for apatite from the Karaçayır carbonatite, and indicates its emplacement within a post-collisional tectonic setting during the late Cretaceous.

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  • MakaleAçık Erişim2020Scopus SJRQ3
    Geochemical, stable (O, c, and b) and radiogenic (sr, nd, pb) isotopic data from the eskişehir-kızılcaören (nw-anatolia) and the malatya-kuluncak (e-central anatolia) f-ree-th deposits, Turkey: Implications for nature of carbonate-hosted mineralization

    Çimen, Okay; Corcoran, Loretta; Kuebler, Corinne; Simonetti, Stefanie S.; Simonetti, Antonio

    In Turkey, the largest fluorine (F)-rare earth element (REE)-thorium (Th) deposits are located within the Eskişehir-Kızılcaören (north-western Anatolia) and the Malatya-Kuluncak (east-central Anatolia) regions, and these are associated with Oligocene extensional alkaline volcanic and Late Cretecaous-Early Paleocene postcollisional intrusive rocks, respectively. In the Kızılcaören region, the basement units include the Triassic Karakaya Complex and the Late Cretaceous oceanic units (Neotethyan suture) that are cut and overlain by phonolite and carbonatite intrusions and lava flows. In the Kuluncak region, the plutonic rocks are mainly composed of syenite, quartz syenite, and rare monzonite, and these cut the late-Cretaceous Karapınar limestone, which hosts the F-REE-Th mineralization in contact zones. A carbonatite sample from the Kızılcaören region displays both a total rare earth element (TREE) concentration (4795 ppm) and δ11B (–6.83‰) isotope composition consistent with mantle-derived carbonatite; whereas it is characterized by heavier δ13C (+1.43‰) and δ18O (+20.23‰) isotope signatures compared to those for carbonatites worldwide. In contrast, the carbonates which host the F-REE-Th mineralization in the Kuluncak region are characterized by lower TREE concentrations (5.13 to 55.88 ppm), and heavier δ13C (–0.14 to –0.75‰), δ18O (+27.36 to +30.61‰), and δ11B (+5.38 to +6.89‰) isotope ratios compared to mantle-derived carbonatites. Moreover, the combined initial87Sr/86Sr (0.70584 to 0.70759) and143Nd/144Nd (0.512238 to 0.512571) isotope ratios for samples investigated here are distinct and much more radiogenic compared to those for carbonatites worldwide, and therefore indicate significant crustal input and/or hydrothermal metasomatic-related alteration. Overall, stable and radiogenic isotope data suggest that the host carbonate rocks for the F-REE-Th mineralization in both the Kızılcaören and the Kuluncak regions consist of hydrothermally metasomatized carbonatite and limestone, respectively. The mineralization in the Kızılcaören region may potentially be related to carbonatite magmatism, whereas the mineralization in the Kuluncak region, which most likely formed through interactions between the plutonic rocks and surrounding limestone at contact metamorphism zone, involved hydrothermal/magmatic fluids associated with extensive postcollisional magmatism.

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  • MakaleYalnız künye2019Scopus SJRQ1
    Combined boron, radiogenic (Nd, Pb, Sr), stable (C, O) isotopic and geochemical investigations of carbonatites from the Blue River Region, British Columbia (Canada): Implications for mantle sources and recycling of crustal carbon

    Çimen, Okay; Kuebler, Corinne; Simonetti, Stefanie S.; Corcoran, Loretta; Mitchell, Roger; Simonetti, Antonio

    This study reports the combined major, minor and trace element compositions, and stable (C, O), radiogenic (Nd, Pb, and Sr) isotopic compositions, and first δ11B isotopic data for the Fir, Felix, Gum, and Howard Creek carbonatites from the Blue River Region, British Columbia (Canada). These sill-like occurrences were intruded into Late Proterozoic strata during rifting and extensional episodes during the Late Cambrian and Devonian -Mississippian, and subsequently deformed and metamorphosed to amphibolite grade in relation to a collisional-type tectonic environment. The carbonatites at Fir, Gum, and Felix contain both calcite and dolomite, whereas the carbonatite at Howard Creek contains only calcite. The dolomite compositions reported here are consistent with those experimentally determined by direct partial melting of metasomatized peridotitic mantle. The combined major and trace element compositions and δ13CPDB (−5.37 to −4.85‰) and δ18OSMOW (9.14 to 9.62‰) values for all the samples investigated are consistent with those for primary igneous carbonate and support their mantle origin. However, these signatures cannot be attributed to closed system melt differentiation from a single parental melt. The initial Nd, Pb, and Sr isotopic ratios are highly variable and suggest generation from multiple, small degree parental melts derived from a heterogeneous mantle source. The δ11B values for carbonates from Felix, Gum, and Howard Creek vary between −8.67 and −6.36‰, and overlap the range for asthenospheric mantle (−7.1 ± 0.9‰), whereas two samples from Fir yield heavier values of −3.98 and −2.47‰. The latter indicate the presence of recycled crustal carbon in their mantle source region, which is consistent with those for young (<300 Ma) carbonatites worldwide. The radiogenic and B isotope results for the Blue River carbonatites are compared to those from contrasting, anorogenic tectonic settings at Chipman Lake, Fen, and Jacupiranga, and indicate that similar upper mantle sources are being tapped for carbonatite melt generation. The pristine, mantle-like δ11B values reported here for the Blue River carbonatites clearly demonstrate that this isotope system is robust and was not perturbed by post-solidification tectono-metamorphic events. This observation indicates that B isotope signatures are a valuable tool for deciphering the nature of the upper mantle sources for carbonates of igneous origin.

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