Mineralization of the Tuwu Porphyry Cu Deposit in Eastern Tianshan, NW China: Insights From In Situ Trace Elements of Chlorite and Pyrite

The Tuwu porphyry copper deposit is located on the Dananhu-Haerlik island arc in eastern Tianshan, NW China. Based on geology, petrology, and in situ trace element studies of pyrite and chlorite, we redefined the characteristics of hydrothermal fluids and the following three mineralization stages: premineralization stage (stage Ⅰ), porphyry metallogenic stage (stage Ⅱ), and superimposed transformation stage (stage Ⅲ). Pyrite stage Ⅰ (Py-I) has the highest Co/Ni ratios, and the precipitation crystallization of chlorite (Chl-I2) has the similar rare earth element distribution patterns with those of volcanic rocks Carboniferous Qieshan (CQ), indicating intense volcanic hydrothermal activity. The Co/Ni ratios of Py-II1 and Py-II2 (stage Ⅱ) tend to decrease over time. Moreover, the rare earth element (REE) distribution patterns of Chl-II have similar LREE enrichment, and the Eu anomalies in Chl-II1, Chl-II2, and Chl-II3 range from positive to negative. The initial ore-forming fluid was mainly magmatic hydrothermal fluid, and with the late-stage addition of meteoric water and continuous sulfide precipitation, the trace element composition of the fluid changed, and the whole system became more oxidizing. Py-III (stage Ⅲ) has the lowest Co/Ni ratios, and the REE distribution pattern of Chl-III is characterized by LREE enrichment. Moreover, the Chl-III shows obvious shear deformation characteristics. The results indicate that the host rocks experienced intensely superimposed reformation. By combining and integrating our results with the regional evolution processes in the eastern Tianshan, we propose that the Tuwu porphyry deposit has undergone magmatic hydrothermal and metamorphic hydrothermal processes. Volcanism (stage Ⅰ) provided the space and initial conditions for the emplacement of the metallogenic body. With the emplacement of the plagiogranite porphyry (stage Ⅱ), the main copper mineralization occurred in the porphyry and surrounding rocks. After porphyry mineralization (stage Ⅲ), regional ductile shearing and collisional compression led to a copper reaction, and its accumulation along the faults formed an ore shoot.

Ediacaran initial subduction and Cambrian slab rollback of the Junggar Ocean: New evidence from igneous tectonic blocks and gabbro enclave in Early Palaeozoic accretionary complexes, southern West Junggar, NW China

New zircon U–Pb ages and whole-rock chemical data from four adakitic and two non-adakitic igneous rocks as tectonic blocks in the southern West Junggar accretionary complexes, northwestern China and one gabbro enclave in adakitic block provide further constraints on the initial subduction and following rollback process of the Junggar Ocean as part of southern Palaeo-Asian Ocean. The oldest adakitic monzonite in Tangbale is intruded by the non-adakitic quartz monzonite at 549 Ma, and the youngest adakitic diorite in Tierekehuola formed at 520 Ma. The Ediacaran–Cambrian magmatism show a N-wards younger trend. The high-SiO2 adakitic rocks have high Sr (300–663 ppm) and low Y (6.68–12.2 ppm), with Sr/Y = 40–84 and Mg no. = 46–60, whereas the non-adakitic rocks have high Y (13.2–22.7 ppm) and Yb (2.32–2.92 ppm), with Mg no. = 36–40. The gabbro has high MgO (14.81–15.11 wt%), Co (45–48 ppm), Cr (1120–1360 ppm) and Ni (231–288 ppm), with Mg no. = 72–73. All the samples show similar large-ion lithophile element (LILE) and light rare earth element (LREE) enrichment and Nb, Ta, Ti and varying Zr and Hf depletion, suggesting that they were formed in a subduction-related setting. The adakitic rocks were produced by partial melting of subducted oceanic slab, but the melts were modified by mantle wedge and slab-derived fluids; the non-adakitic rocks were likely derived from partial melts of the middle-lower arc crust; and the gabbro originated from the mantle wedge modified by slab-derived fluids. The magmatism could have been generated during the Ediacaran initial subduction and Cambrian slab rollback of the Junggar Ocean.

Combined In Situ Chemical and Sr Isotopic Compositions and U–Pb Ages of the Mushgai Khudag Alkaline Complex: Implications of Immiscibility, Fractionation, and Alteration

The Mushgai Khudag complex consists of numerous silicate volcanic-plutonic rocks including melanephelinites, theralites, trachytes, shonkinites, and syenites and also hosts numerous dykes and stocks of magnetite-apatite-enriched rocks and carbonatites. It hosts the second largest REE–Fe–P–F–Sr–Ba deposit in Mongolia, with REE mineralization associated with magnetite-apatite-enriched rocks and carbonatites. The bulk rock REE content of these two rock types varies from 21,929 to 70,852 ppm, which is much higher than that of syenites (716 ± 241 ppm). Among these, the altered magnetite-apatite-enriched rocks are characterized by the greatest level of REE enrichment (58,036 ± 13,313 ppm). Magmatic apatite from magnetite-apatite-enriched rocks is commonly euhedral with purple luminescence, and altered apatite displays variable purple to blue luminescence and shows fissures and hollows with deposition of fine-grained monazite aggregates. Most magmatic apatite within syenite is prismatic and displays oscillatory zoning with variable purple to yellow luminescence. Both magmatic and altered apatite from magnetite-apatite-enriched rocks were dated using in situ U–Pb dating and found to have ages of 139.7 ± 2.6 and 138.0 ± 1.3 Ma, respectively, which supports the presence of late Mesozoic alkaline magmatism. In situ 87Sr/86Sr ratios obtained for all types of apatite and calcite within carbonatite show limited variation (0.70572–0.70648), which indicates derivation from a common mantle source. All apatite displays steeply fractionated chondrite-normalized REE trends with significant LREE enrichment (46,066 ± 71,391 ppm) and high (La/Yb)N ratios ranging from 72.7 to 256. REE contents and (La/Yb)N values are highly variable among different apatite groups, even within the same apatite grains. The variable REE contents and patterns recorded by magmatic apatite from the core to the rim can be explained by the occurrence of melt differentiation and accompanying fractional crystallization. The Y/Ho ratios of altered apatite deviate from the chondritic values, which reflects alteration by hydrothermal fluids. Altered apatite contains a high level of REE (63,912 ± 31,785 ppm), which are coupled with increased sulfur and/or silica contents, suggesting that sulfate contributes to the mobility and incorporation of REEs into apatite during alteration. Moreover, altered apatite is characterized by higher Zr/Hf, Nb/Ta, and (La/Yb)N ratios (179 ± 48, 19.4 ± 10.3, 241 ± 40, respectively) and a lack of negative Eu anomalies compared with magmatic apatite. The distinct chemical features combined with consistent Sr isotopes and ages for magmatic and altered apatite suggest that pervasive hydrothermal alterations at Mushgai Khudag are most probably being induced by carbonatite-evolved fluids almost simultaneously after the alkaline magmatism.

Mineralogy of Dolomite Carbonatites of Sevathur Complex, Tamil Nadu, India

The main mass of the Sevathur carbonatite complex (Tamil Nadu, India) consists of dolomite carbonatite with a small number of ankerite carbonatite dikes. Calcite carbonatite occurs in a very minor amount as thin veins within the dolomite carbonatite. The age (207Pb/204Pb) of the Sevathur carbonatites is 801 ± 11 Ma, they are emplaced within the Precambrian granulite terrains along NE–SW trending fault systems. Minor minerals in dolomite carbonatite are fluorapatite, phlogopite (with a kinoshitalite component), amphibole and magnetite. Pyrochlore (rich in UO2), monazite-Ce, and barite are accessory minerals. Dolomite carbonatite at the Sevathur complex contains norsethite, calcioburbankite, and benstonite as inclusions in primary calcite and are interpreted as primary minerals. They are indicative of Na, Sr, Mg, Ba, and LREE enrichment in their parental carbonatitic magma. Norsethite, calcioburbankite, and benstonite have not been previously known at Sevathur. The hydrothermal processes at the Sevathur carbonatites lead to alteration of pyrochlore into hydropyrochlore, and Ba-enrichment. Also, it leads to formation of monazite-(Ce) and barite-II.

The petrological and geochemical study of granitoid rocks from Mashhad area, Iran: Evidence for the Late Triassic Collisional Belt Northeast of Iran

<p>Mashhad granitoid complex is part of the northern slope of the Binalood Structural Zone (BSZ), Northeast of Iran, which is composed of granitoids and metamorphic rocks. This research presents new petrological and geochemical whole-rock major and trace elements analyses in order to determine the origin of granitoid rocks from Mashhad area. Field and petrographic observations indicate that these granitoid rocks have a wide range of lithological compositions and they are categorized into intermediate to felsic intrusive rocks (SiO<sub>2</sub>: 57.62-74.39 Wt.%). Qartzdiorite, tonalite, granodiorite and monzogranite are common granitoids with intrusive pegmatite and aplitic dikes and veins intruding them. Based on geochemical analyses, the granitoid rocks are calc-alkaline in nature and they are mostly peraluminous. On geochemical variation diagrams (major and minor oxides versus silica) Na<sub>2</sub>O and K<sub>2</sub>O show a positive correlation with silica while Al<sub>2</sub>O<sub>3</sub>, TiO<sub>2</sub>, CaO, Fe<sub>2</sub>O<sub>3</sub>, and MgO show a negative trend. Therefore fractional crystallization played a considerable role in the evolution of Mashhad granitoids. Based on the spider diagrams, there are enrichments in LILE and depletion in HFSE. Low degrees of melting or crustal contamination may be responsible for LILE enrichment. Elements such as Pb, Sm, Dy and Rb are enriched, while Ba, Sr, Nd, Zr, P, Ti and Yb (in monzogranites) are all depleted. LREE enrichment and HREE depletion are observed in all samples on the Chondrite-normalized REE diagram. Similar trends may be evidence for the granitoids to have the same origin. Besides, LREE enrichment relative to HREE in some samples can indicate the presence of garnet in their source rock. Negative anomalies of Eu and Yb are observed in monzogranites. Our results show that Mashhad granitoid rocks are orogenic related and tectonic discrimination diagrams mostly indicate its syn-to-post collisional tectonic setting. No negative Nb anomaly compared with MORB seems to be an indication of non-subduction zone related magma formation. According to the theory of thrust tectonics of the Binalood region, the oceanic lithosphere of the Palo-Tethys has subducted under the Turan microplate. Since the Mashhad granitoid outcrops are settled on the Iranian plate, this is far from common belief that these granitoid rocks are related to the subduction zones and the continental arcs. The western Mashhad granitoids show more mafic characteristics and are possibly crystallized from a magma with sedimentary and igneous origin. Thus, Western granitoid outcrops in Mashhad are probably hybrid type and other granitoid rocks, S and SE Mashhad are S-type. Evidences suggest that these continental collision granitoid rocks are associated with the late stages of the collision between the Iranian and the Turan microplates during the Paleo-Tethys Ocean closure which occurred in the Late Triassic.</p>

Distribution of rare-earth elements in rock-forming minerals of corundum-bearing rocks of the Khitoostrov deposit (North Karelia)

The distribution of rare-earth elements (SIMS method) in minerals from the rocks of the Khitoostrov occurrence (Belomorian mobile belt of Eastern Fennoscandia) was studied: corundum-bearing metasomatites with anomalous isotopically light oxygen and hydrogen and garnet amphibolites after gabbro with normal isotopic composition. The study was accompanied by estimates of P-T parameters of rock formation using multi-equilibrium thermobarometry (TWEEQU method). Temperatures calculated for garnet amphibolites after gabbro fall within the range of 730–770 ° C, pressures - 13–14 kbar; for corundum-bearing rocks, temperatures were 680–710 ° C, pressures - 6.5–7.5 kbar. Corundum-bearing rocks were formed at slightly lower temperatures and at significantly lower pressures than garnet amphibolites after gabbro. The REE distribution spectra in garnets from apogabbroic amphibolites are characterized by a clearly pronounced slope from light to heavy REE, while in garnets from corundum-bearing rocks they have a less pronounced positive slope, which is associated with a noticeable enrichment of garnets in LREE and an insignificant depletion of HREE. Calcium amphiboles from corundum-bearing rocks are significantly enriched in rare-earth elements as compared to amphiboles from garnet amphibolites after gabbro, especially LREE (by more than an order of magnitude) and, to a lesser extent, MREE. Plagioclases from corundum-bearing rocks are also enriched in LREE against the background of garnet amphibolites. Thus, in all the studied minerals of corundum-bearing rocks LREE enrichment is recorded. It isn’t manifested in the minerals of amphibolites and, obviously, isn’t related to the difference in P-T parameters of rock formation. Consequently, LREE was transferred by a specific fluid during mineral-forming processes, which led to the formation of metasomatites with an anomalous isotopic composition of oxygen and hydrogen.

Geochemical and Geochronological Constraints on the Genesis of Ion-Adsorption-Type REE Mineralization in the Lincang Pluton, SW China

Granites are assumed to be the main source of heavy rare-earth elements (HREEs), which have important applications in modern society. However, the geochemical and petrographic characteristics of such granites need to be further constrained, especially as most granitic HREE deposits have undergone heavy weathering. The LC batholith comprises both fresh granite and ion-adsorption-type HREE deposits, and contains four main iRee (ion-adsorption-type REE) deposits: the Quannei (QN), Shangyun (SY), Mengwang (MW), and Menghai (MH) deposits, which provide an opportunity to elucidate these characteristics The four deposits exhibit light REE (LREE) enrichment, and the QN deposit is also enriched in HREEs. The QN and MH deposits were chosen for study of their petrology, mineralogy, geochemistry, and geochronology to improve our understanding of the formation of iRee deposits. The host rock of the QN and MH deposits is granite that includes REE accessory minerals, with monazite, xenotime, and allanite occurring as euhedral inclusions in feldspar and biotite, and thorite, fluorite(–Y), and REE fluorcarbonate occurring as anhedral filling in cavities in quartz and feldspar. Zircon U–Pb dating analysis of the QN (217.8 ± 1.7 Ma, MSWD = 1.06; and 220.3 ± 1.2 Ma, MSWD = 0.71) and MH (232.2 ± 1.7 Ma, MSWD = 0.58) granites indicates they formed in Late Triassic, with this being the upper limit of the REE-mineral formation age. The host rock of the QN and MH iRee deposits is similar to most LC granites, with high A/CNK ratios (>1.1) and strongly peraluminous characteristics similar to S-type granites. The LC granites (including the QN and MH granites) have strongly fractionated REE patterns (LREE/HREE = 1.89–11.97), negative Eu anomalies (Eu/Eu* = 0.06–0.25), and are depleted in Nb, Zr, Hf, P, Ba, and Sr. They have high 87Sr/86Sr ratios (0.710194–0.751763) and low 143Nd/144Nd ratios (0.511709–0.511975), with initial Sr and Nd isotopic compositions of (87Sr/86Sr)i = 0.72057–0.72129 and εNd(220 Ma) = −9.57 to −9.75. Their initial Pb isotopic ratios are: 206Pb/204Pb = 18.988–19.711; 208Pb/204Pb = 39.713–40.216; and 207Pb/204Pb = 15.799–15.863. The Sr–Nd–Pb isotopic data and TDM2 ages suggest that the LC granitic magma had a predominantly crustal source. The REE minerals are important features of these deposits, with feldspars and micas altering to clay minerals containing Ree3+ (exchangeable REE), whose concentration is influenced by the intensity of weathering; the stronger the chemical weathering, the more REE minerals are dissolved. Secondary mineralization is also a decisive factor for Ree3+ enrichment. Stable geology within a narrow altitudinal range of 300–600 m enhances Ree3+ retention.

Lithospheric mantle beneath the Mid-German Crystalline High Variscan unit: Breitenborn (Vogelsberg, Central Germany) case study

<p>The Cenozoic volcanic field of Vogelsberg (part of CEVP in Central Germany) is located at the northern extension of the Upper Rhine Graben. Three Variscan basement units underlie Vogelsberg from NW to SE: the Rheno-Hercynian Zone, the Northern Phyllite Zone and the Mid-German Crystalline High. Xenoliths from the Breitenborn basanite sample lithospheric mantle (LM) beneath the Mid-German Crystalline High.</p><p>The Breitenborn suite comprises xenoliths of 3-7.5 cm in diameter: clinopyroxene-poor spinel lherzolites, spinel harzburgites and clinopyroxenites. Peridotites exhibit different degrees of deformation: porphyroclastic textures, foliation development and grain size reduction. Mineral components are chemically homogenous at the grain and xenolith scale. Forsterite content (Fo) in olivine ranges between 89.8 and 91.5% with exception of Fo ~89.0% in one xenolith. Orthopyroxene (opx) is characterized by Mg# of 0.900-0.923 and 0.06-0.18 atoms of Al pfu, whereas clinopyroxene (cpx) by Mg# of 0.894-0.931 and 0.11-0.23 atoms of Al pfu. Spinel Cr# ranges from 0.18 to 0.45. Clinopyroxenites exhibit protogranular textures with no deformation. They are significantly less magnesian (cpx Mg# 0.834-0.863) and more aluminous (0.25-0.31 atoms of Al pfu) than peridotites.</p><p>Peridotite cpx REE patterns show different degree of enrichment in LREE, except two xenoliths being strongly depleted in LREE. Opx from those two xenoliths exhibits patterns steeply depleted from HREE to LREE. The remaining opx shows mild depletion in LREE relative to HREE or slight LREE enrichment.</p><p>Temperatures calculated using REE content (T<sub>REE</sub>) [1] range between 1030 and 1130°C for most of the xenoliths and show that pyroxenes are in REE equilibrium. Exceptions are LREE-depleted xenoliths which have 940-975°C and exhibit no LREE equilibrium. Temperatures calculated on the basis of pyroxene major element contents (T<sub>BKN</sub>) [2] are ~40-140°C lower than T<sub>REE</sub>.</p><p>During Cenozoic rifting which formed the Upper Rhine Graben, a diversity of melts interacted with the LM beneath Vogelsberg. LREE-enriched cpx and opx patterns suggest metasomatic alteration of LM by alkaline melts, which is typical of other studied sites in the area. A calculated hypothetical melt in equilibrium with clinopyroxenite cpx patterns resembles those of basanites and alkaline basalts occurring in Vogelsberg, which were possibly involved in the alkaline metasomatism of the LM. Varying discrepancy between T<sub>REE</sub> and T<sub>BKN</sub> indicate that the xenoliths experienced cooling after melt metasomatism of the LM, which was not followed by recrystallisation. Different degrees of LREE enrichment and gradual changes in major element compositions of peridotite minerals indicate the chromatographic character of the alkaline metasomatism. Strongly LREE-depleted cpx and opx patterns probably are effects of metasomatism by melts derived from depleted MORB mantle, which are typical products of advanced melting in continental rifting environments.</p><p> </p><p>The study was funded by Polish National Science Centre to MZ (project UMO-2018/29/N/ST10/00259). EPMA analyses were done within the frame of the Polish-Austrian project WTZ PL 08/2018. MZ acknowledges the DAAD fellowship at the Goethe University in Frankfurt.</p><p> </p><p>References</p><p>[1] Liang Y. et al. (2013). GeochimCosmochimAc 102, 246–260.</p><p>[2] Brey G. & Köhler T. (1990). JPetrol 31, 1353–1378.</p>

Petrogenesis of high Ba–Sr plutons with high Sr/Y ratios in an intracontinental setting: evidence from Early Cretaceous Fushan monzonites, central North China Craton

Geochronological, major and trace element, and Sr–Nd–Hf isotopic data are reported for the monzonitic rocks of the Fushan pluton in the Taihang Mountains, central North China Craton, in order to investigate their sources, petrogenesis and tectonic implications. Zircon U–Pb dating results reveal that the Fushan pluton was emplaced during the Early Cretaceous (∼126–124 Ma). The monzonites and quartz monzonites are mainly characterized by calc-alkaline and magnesian features and display light rare earth element (LREE) enrichment and flat heavy REE (HREE) patterns with slightly positive Eu anomalies. They have similar whole-rock initial 87Sr/86Sr ratios (0.70653–0.70819), εNd(t) values (−13.6 to −18.6) and zircon εHf(t) values (−21.8 to −17.3). The primary magma of the Fushan pluton was derived from the partial melting of a spinel-facies amphibole-bearing ancient enriched lithospheric mantle. The monzonitic rocks also have high Ba–Sr and low Y and Yb contents, with high Sr/Y and La/Yb ratios. These geochemical features of monzonitic rocks are not only inherited from the magma source but also significantly enhanced by crystal fractionation during magmatic evolution; e.g. hornblende fractionation increased the Ba–Sr concentrations and Sr/Y ratios. During the Early Cretaceous, the slab sinking and roll-back of the Palaeo-Pacific Plate could have created an ancient big mantle wedge beneath East Asia and induced a lithospheric extensional process in the central North China Craton within an intracontinental setting.