Nb–Ta mineralization in Ti-oxide minerals from the Bagolyhegy Metarhyolite Formation (Bükk Mountains, NE Hungary)

The foliated low-grade metamorphic rocks of the Triassic Bagolyhegy Metarhyolite Formation, mainly of pyroclastic origin, host post-metamorphic quartz-albite veins containing abundant tourmaline and occasionally rutile/ilmenite. The study of the Ti-oxide-mineralized veins with SEM-EDX revealed an unusual mineral assemblage comprising fine-grained Nb–Ta-bearing oxides (columbite-tantalite series, fluorcalciomicrolite and other Nb–Ti–Y–Fe-REE-oxide minerals) intergrown with Nb-rich polymorphs of TiO2 (anatase, rutile), ilmenite and zircon enriched with hafnium. This high field strength elements (HFSE)-bearing paragenesis is unexpected in this lithology, and was not described from any formation in the Paleozoic-Mesozoic rock suite of the Bükk Mountains (NE Hungary) before. The host metavolcanics are significantly depleted in all HFSE compared to the typical concentrations in felsic volcanics and the mineralized quartz-albite veins have even lower Ti–Nb–Ta concentration than the host rock, so the mineralization does not mean any enrichment. From proximal outcrops of the Triassic Szentistvánhegy Metavolcanics, potassic metasomatized lenses with albite-quartz vein fillings containing rutile/ilmenite are known. We studied them for comparison, but they only contain REE mineralization (allanite-monazite-xenotime); the Nb–Ta-content of Ti-oxide minerals is undetectably low. LA-ICP-MS measurements for U–Pb dating of Hf-rich zircon of the Nb–Ta-rich mineral assemblage gave 71.5 ± 5.9 Ma as lower intercept age while dating of allanite of the REE mineralized quartz-albite veins gave 113 ± 11 Ma as lower intercept age. The REE-bearing vein fillings formed during a separate mineralization phase in the Early Cretaceous, while the Nb–Ta mineralization was formed by post-metamorphic alkaline fluids in the Late Cretaceous., controlled by fault zones and fractures.

Quantifying metasomatic high-field-strength and rare-earth element transport from alkaline magmas

Alkaline igneous rocks host many global high-field-strength element (HFSE) and rare-earth element (REE) deposits. While HFSEs are commonly assumed to be immobile in hydrothermal systems, transport by late-stage hydrothermal fluids associated with alkaline magmas is reported. However, the magnitude of the flux and the conditions are poorly constrained and yet essential to understanding the formation of REE-HFSE ores. We examined the alteration of country rocks (“fenitization”) accompanying the emplacement of a syenite magma at Illerfissalik in Greenland, through analysis of changes in rock chemistry, mineralogy, and texture. Our novel geochemical maps show a 400-m-wide intrusion aureole, within which we observed typically tenfold increases in the concentrations of many elements, including HFSEs. Textures suggest both pervasive and structurally hosted fluid flow, with initial reaction occurring with the protolith’s quartz cement, leading to increased permeability and enhancing chemical interaction with a mixed Ca-K-Na fenitizing fluid. We estimated the HFSE masses transferred from the syenite to the fenite by this fluid and found ~43 Mt of REEs were mobilized (~12% of the syenite-fenite system total rare-earth-oxide [TREO] budget), a mass comparable to the tonnages of some of the world’s largest HFSE resources. We argue that fenite can yield crucial information about the tipping points in magma evolution because retention and/or loss of volatile-bonded alkali and HFSEs are key factors in the development of magmatic zirconosilicate-hosted HFSE ores (e.g., Kringlerne, at Ilímaussaq), or the formation of the syenite-hosted Nb-Ta-REE (Motzfeldt-type) roof-zone deposits.

Petrography and Geochemistry of Gabbroic Rock from the Penjwin Ophiolite, Kurdistan Region, Northeastern Iraq

The gabbroic rocks as a part of Zagros ophiolite are exposed in northeastern Iraq, Penjwin area. These rocks with granular to ophitic textures are widely distributed without metamorphic halos. The main minerals are plagioclase (An90-99), olivine, clinopyroxene (Wo27-47 En 45-64 Fs8-14) and orthopyroxene (Wo2 En78 Fs20) respectively based on the abundances. The major elements show a broad range of compositional variations, with SiO2 (46.2–50.9 wt. %), and low concentrations Na2O (0.15–0.62 wt. %), K2O (0.01–0.03 wt. %) and TiO2 (0.06–0.2) and high concentrations, Al2O3 (6.4–19.75 wt. %), total Fe2O3 (6.29–11.6 wt. %), MgO (9.63–24.5 wt. %), CaO (8.02–18 wt. %) and low alkali contents (Na2O + K2O = 0.16–0.65 wt. %). On Ti-V diagram, all of the gabbroic samples have Ti/V less than 10 and consequently fall in the low Ti- Island arc tholeiitic. Whole rocks chemistry shows a depletion of High field strength elements in comparison with the primitive mantle with an arched upward rare earth elements pattern, characterized by light rare earth elements depletion (La N/Sm N = 0.05–0.8) and enrichment in the High field strength elements. Whole rocks chemistry, mineral paragenesis and chemistry of these rocks are more consistent with tholeiitic magma series. Based on our findings in this research, the primary magma has been produced from the depleted mantle with a high degree of partial melting.

Supplemental Material: Quantifying metasomatic high-field-strength and rare-earth element transport from alkaline magmas

Petrographic information, parameterization of the Grant model, description of the HFSE tonnage estimation method, and supplemental tables of whole-rock data, standardization, and HFSE volume-tonnage calculations.<br>

Supplemental Material: Quantifying metasomatic high-field-strength and rare-earth element transport from alkaline magmas

Petrographic information, parameterization of the Grant model, description of the HFSE tonnage estimation method, and supplemental tables of whole-rock data, standardization, and HFSE volume-tonnage calculations.<br>

Petrogenesis of Triassic Caojian A-type rhyolites and associated I-type granites in the southeastern Tibetan Plateau: rejuvenation of crystal mush

The orogenic process and crustal growth of the Changning–Menglian Palaeo-Tethys orogenic belt in the southeastern Tibetan Plateau is not fully understood. Triassic Caojian rhyolites and granites occur extensively in this orogenic belt and represent important constraints for this issue. This study aims to examine the relationships between the Triassic Caojian rhyolites and granites and to gain a better understanding of their possible petrogenesis. The study used zircon U–Pb geochronology, trace element analyses and Sr–Nd–Hf isotope data to better understand the relationships and possible origin of the rhyolites and granites. Recent zircon U–Pb ages indicated that the Caojian rhyolites were emplaced at 227.2 Ma, whereas age estimates for Caojian granites were slightly older (233.4–236.9 Ma). The Caojian rhyolites are enriched in large-ion lithophile elements and high-field-strength elements, with elevated FeOtot/MgO and Ga/Al ratios. However, they are significantly depleted in Ba, Sr, Eu, P and Ti. These geochemical characteristics indicate that they have an A-type affinity. Furthermore, the Caojian granites comprise biotite monzogranites and granodiorites and show unfractionated composition. Mineralogically, the Caojian granites were found to contain diagnostic I-type minerals such as hornblende. Geochemical data suggest that the petrogenesis of the Triassic Caojian rhyolites is characterized by rejuvenation of crystal mush represented by the Triassic Caojian granites. The necessary thermal input was supplied by mafic magma. This magmatic evolution was likely related to lithospheric delamination and upwelling of the asthenosphere during the Mid- to Late Triassic, forming post-collisional I-type granites and A-type volcanics in the Changning–Menglian Palaeo-Tethys orogenic belt.

Sediment-Peridotite Reaction Controls Fore-Arc Metasomatism and Arc Magma Geochemical Signatures

Subduction of oceanic crust buries an average thickness of 300–500 m of sediment that eventually dehydrates or partially melts. Progressive release of fluid/melt metasomatizes the fore-arc mantle, forming serpentinite at low temperatures and phlogopite-bearing pyroxenite where slab surface reaches 700–900 °C. This is sufficiently high to partially melt subducted sediments before they approach the depths where arc magmas are formed. Here, we present experiments on reactions between melts of subducted sediments and peridotite at 2–6 GPa/750–1100 °C, which correspond to the surface of a subducting slab. The reaction of volatile-bearing partial melts derived from sediments with depleted peridotite leads to separation of elements and a layered arrangement of metasomatic phases, with layers consisting of orthopyroxene, mica-pyroxenite, and clinopyroxenite. The selective incorporation of elements in these metasomatic layers closely resembles chemical patterns found in K-rich magmas. Trace elements were imaged using LA-ICP-TOFMS, which is applied here to investigate the distribution of trace elements within the metasomatic layers. Experiments of different duration enabled estimates of the growth of the metasomatic front, which ranges from 1–5 m/ky. These experiments explain the low contents of high-field strength elements in arc magmas as being due to their loss during melting of sedimentary materials in the fore-arc.