High Oxygen Fugacity Research Articles

Garnet clinopyroxenite formation via amphibole-dehydration in continental arcs: Evidence from Fe isotopes

Lower-crustal garnet clinopyroxenite (sometimes termed “arclogite”) fractionation in thick-crustal (>35 km) arc settings presents a compelling model to explain Fe-depletion trends, high oxygen fugacity, and evidence of recent delamination observed in many continental arcs. However, the origin of the garnet clinopyroxenites via igneous or metamorphic processes remains unclear. Due to the preferential incorporation of light Fe isotopes in garnet relative to clinopyroxene or amphibole, Fe isotopes are ideally suited for studying the effects of garnet fractionation on magmatic systems. Here, we present whole-rock and mineral Fe isotope data from a suite of lower to mid/upper-crustal Andean xenoliths from Mercaderes, Colombia. This data is combined with petrography, major and trace element mineral and whole-rock chemistry, geothermobarometry, and thermodynamic modeling to explore the xenoliths' petrogenesis and the Northern Andes' crustal structure. Whole-rock samples display a narrow range of Fe isotope compositions (δ56Fe = –0.02 to +0.11 ‰), which do not correlate with lithology, chemistry, or pressure-temperature conditions. This result is inconsistent with previous studies predicting the existence of an isotopically light Fe reservoir in the garnet-rich lower Andean crust. Through thermodynamic modeling, we show that the lack of isotopic fractionation in the Mercaderes xenoliths is more consistent with the suite representing a prograde metamorphic sequence, in which amphibole dehydration reactions drive metamorphism of mid/upper-crustal diorite protoliths. While our data do not preclude the presence of garnet clinopyroxenite cumulates at the base of the Andean crust, or that the delamination of such cumulates played an important role in the evolution of the Andes, they do indicate that not all garnet clinopyroxenites are cumulate in origin. Instead, the lower Andean crust represents an amalgamation of igneous and metamorphic rock, with metamorphism of mid-crustal lithologies and partial melting of mafic cumulate roots acting in tandem to drive densification and delamination of the lower crust in a self-feeding mechanism.

Mineralization processes in the Bainaimiao Cu-Au deposit in Inner Mongolia, China: Constraints from geology, geochronology, and mineralogy

The Central Asian Orogenic Belt underwent complex tectonic processes and is one of the most intensely accretionary areas globally. Porphyry copper deposits within the belt were likely subjected to deformation during tectonic processes. The Bainaimiao Cu-Au deposit is a typical example of a deformed porphyry deposit whose formation processes include a porphyry emplacement (Event I), a greenschist facies metamorphism (Event II), and a brittle deformation (Event III). Geochronology and trace element geochemistry of zircon, volatiles of magmatic apatite, along with the assemblages, textures, abundances, and compositions of phyllosilicates from these three events were investigated to unveil the physicochemical conditions under which the key geological events relevant to the deposit formation took place. LA-ICP-MS zircon U-Pb dating shows that the granodiorite porphyry in the northern and southern zones formed at 447.4 ± 1.6 to 445.8 ± 3.6 Ma and 436.1 ± 3.8 to 434.1 ± 3.3 Ma, respectively. The granodiorite porphyry in the northern zone has higher oxygen fugacity and Clmelt content but similar Smelt and Fmelt contents compared to the granodiorite porphyry in the southern zone. Microscopic and mineralogic observations point to Event I to be of high plagioclase (22–67 vol%) and quartz (6–40 vol%) content with a range of hydrothermal minerals related to potassic, phyllic, and propylitic alterations. Event II features high amphibole (38–83 vol%) or epidote-chlorite (up to 77 vol%) content with minerals precipitating along the schistosity planes. Event III is characterized by wide veins (3–80 cm) and the highest quartz (61–65 vol%) and calcite (12–19 vol%) content. Geothermometry results show the temperature of potassic and phyllic alterations of Event I to be ∼622 °C and ∼288 °C, respectively. Based on geothermometry and P-T pseudosections, the temperatures of metamorphism and metallic precipitation of Event II were ∼271–634 °C and 297–328 °C, respectively. Both mechanical and chemical mobilization of metallic elements results in Cu mineralization during Event II. The metallic precipitation temperatures of Event III spanned from 297 to 328 °C according to chlorite geothermometry. The ratios of Fe3+/Fetotal and Mg/(Mg + Fetotal) of biotite, chlorite Fe/(Fe + Mg), and white K-mica composition show the mineralizing fluid of Event III to be the most oxidized while that of Event II is the most reduced, F-rich and features the lowest water/rock ratio. This study suggests that deformation processes can increase the Cu mineralization grade of the deformed porphyry deposits through mobilization and re-precipitation of metallic elements.

An estimate of chlorine fugacity in the low water fluid of the system С-О-(Н)-NaCl in the cumulus of ultrabasic-basic intrusions

At high PT parameters of the cumulates of ultramafic-mafic intrusions at low fO2 (below the QFM buffer), platinum dissolves in the fluid with CO as a carbonyl complex of the native metal. The high solubility of platinum as PtCl2 in brines with NaCl, which is associated with the formation of low-sulfide PGE deposits, is achieved at high oxygen fugacity (above the NNO buffer). It is assumed that at low oxygen fugacity in the low water CO–CO2 fluid, native Pt can also be converted into a cation-soluble form by chlorination. Experimental data (Р = 200 MPa, Т = 950oC, fO2 QFM and fluid CO–CO2) on the reaction of NaCl with magnetite and chromite, accessor minerals of mafic-ultramafic intrusions, with the formation of iron and chromium chlorides are presented. As shown by thermodynamic calculations, the equilibrium in the FeCl3–FeCl2 pair provides the high chlorine fugacity (fCl2). This fugacity is only 3–4 orders of magnitude lower than fCl2 in the Pt–PtCl2 equilibrium and 2.5–3 orders of magnitude higher than in the aqueous fluid 1 M HCl at the same P–T–fO2 parameters.

Geochemical characteristics of olivine and clinopyroxene in parental mafic–ultramafic rocks from the Yuanshishan Ni-Co laterite deposit in Qinghai Province, NW China

Yuanshishan is a Ni-Co laterite deposit that occurs in the Lajishan tectonic zone of the South Qilian orogenic belt, NW China. Ni–Co mineralization took place during the weathering of the parental mafic–ultramafic rocks. Little is known about the petrogenesis of these parent rocks. Therefore, field and petrographic investigations, together with in situ major and trace element analyses, were carried out on olivine and clinopyroxene from unweathered mafic–ultramafic rocks in the Yuanshishan Ni-Co deposit. The results show that olivine (Ni 963–2674 ppm, Co 52.7–245 ppm) is richer in Co and Ni than clinopyroxene (Ni 155–203 ppm, Co 23.1–32.5 ppm) in the Yuanshishan mafic–ultramafic rocks. The chromite (Ni 98.8–892 ppm, Co 836–1062 ppm) show higher Co and Ni than clinopyroxene, but has lower Ni but higher Co than olivine. Therefore, olivine and chromite are two main Co and Ni rich minerals in the parent rocks of Yuanshishan. A compositional comparison of olivine and clinopyroxene from the Yuanshishan deposit to those from other magmatic sulfide deposits reveals that the Yuanshishan parent magma is relatively poor in Ni and rich in Co. Olivine in the dunite of Yuanshishan has a quite high Fo value (95.2–98.3). The Yuanshishan olivine grains also show a positive correlation between Ni content and Ni/Co or Co content, and the correlation with Fo value is not obvious. The Co content shows a negative correlation with the Ni content and Fo value, which are consistent with the mantle olivine characteristics. Furthermore, the Li, Sc, V contents in olivine are lower than 10 ppm, indicating that the magma originated from the mantle. The Al, Si, Ti, Ca, and Na contents in clinopyroxene indicate that the original magma may have been subalkaline basaltic melt. Using an olivine-spinel thermometer, the Yuanshishan magma crystallization temperatures are calculated to be 1256–1376 °C. The AlⅣ:AlⅥ ratio (0.7–6.0) and Eu/Eu* value (0.9–1.4) of the clinopyroxene indicate that the Yuanshishan mafic–ultramafic rocks were formed under conditions of low to medium pressure and high oxygen fugacity. Moreover, the geochemical discriminant diagrams of clinopyroxene indicate that these rocks possibly formed in an island arc setting.

The Yadovitaya fumarole, Tolbachik volcano: A comprehensive mineralogical and geochemical study and driving factors for mineral diversity

Active volcanic fumaroles are one of the most spectacular natural objects in terms of mineral diversity. The Great Tolbachik Fissure Eruption (GTFE) (Kamchatka) fumaroles are renowned for its exceptional number of mineral species. The total number of minerals that have been reliably identified from this particular locality exceeds 400, which is approximately 6.5 % of all known minerals to date. In this study, we employ a comprehensive approach (bulk chemistry, microprobe analysis, powder X-ray diffraction, HR X-ray computed tomography, and 34S, 18O, and 65Cu isotope measurements) to study the distribution of primary exhalation and secondary mineral assemblages and to reveal the driving factors responsible for the unique mineral diversity in the Yadovitaya fumarole. High oxygen fugacity, the interaction of minerals with atmospheric oxygen and water from seasonal precipitation (leading to abundant hydrated mineral associations), temperature conditions controlling the spatial distribution of mineral-forming components, gas-rock interactions, and basaltic scoria morphology perfect for the crystallization of various minerals are some of the factors revealed. The combination of these factors caused a stepwise mineralization resulting in 12 zones of the Yadovitaya fumarole with characteristic mineral assemblages. The described mineralogy of the Yadovitaya fumarole demonstrates a consistent spatial evolution of fumarolic mineral assemblages that vary in complexity, chemistry, and interaction patterns with the surrounding environment. The examination of mineralogical and geochemical data yields novel insights into the active volcanic systems that are associated with the formation of distinct oxidation-type fumaroles.

Geochronology and Geochemistry of Granodiorite Porphyry in the Baoshan Cu-Pb-Zn Deposit, South China: Insights into Petrogenesis and Metallogeny

The Baoshan Cu-Pb-Zn deposit is situated at the intersection of the Qin-Hang Cu polymetallic and Nanling W-Sn polymetallic metallogenic belts. The age, lithology, petrogenesis, and tectonic setting of granodiorite porphyry within the deposit remain subjects of debate. Additionally, there is a lack of comparative studies with the W-Sn-related granites in the region. This study conducted whole-rock major and trace element analysis, Sr-Nd isotope analysis, and zircon U-Pb dating on the Baoshan granodiorite porphyry. The zircon U-Pb age of the granodiorite porphyry is 162 ± 1 Ma. The whole-rock SiO2 and K2O contents range from 65.87 to 68.21 wt.% and 3.42 to 5.62 wt.%, respectively, indicating that the granodiorite porphyry belongs to high-potassium calc-alkaline I-type granite. The granodiorite porphyry is characterized by enrichment in LREE and depletion in HREE (LREE/HREE ratio = 6.2–21.2). The samples of granodiorite porphyry generally exhibit weak negative Eu anomalies or no Eu anomalies (δEu = 0.62–1.04, mean = 0.82). The (87Sr/86Sr)i and εNd(t) values are 0.707717–0.709506 and −7.54 to −4.87, respectively. The whole-rock geochemical composition and Sr-Nd isotopic values indicate that the magma originated from the partial melting of the Mesoproterozoic ancient crust and Neoproterozoic mafic juvenile lower crust, with the addition of high oxygen fugacity and water-rich lithospheric mantle melts. The source of the granodiorite porphyry in the Baoshan deposit is significantly different from the crust-derived metapelite source of the W-Sn-related granite in the area, indicating that different magma sources might be the main reason for the co-spatial and nearly contemporaneous development of Cu-Pb-Zn and W-Sn mineralization in the southern Hunan region.

Two-stage mineralization of the Jinkeng Sn-Cu deposit in Eastern Guangdong, Southeast China: Response to magmatic activities and tectonic transformation

The Jinkeng Sn-Cu polymetallic deposit in South China consists of two different types of orebodies: 1) NE-striking skarn- and vein-type Cu-Pb-Zn-Sn orebodies in volcanic rocks suffering subsequent ductile shear deformation, and 2) NW-striking quartz-cassiterite-sulfide veins filled in the faults at the porphyritic granodiorite outward from the fine-grained granite which does not exhibit deformation. The relationships among Sn-Cu polymetallic mineralization, regional magmatism, and deformation metamorphism are still controversial. To address it, the geochronological, whole-rock and mineral geochemical research along with the detailed field investigation were conducted in this study. Our zircon U-Pb dating results show that the volcanic rocks formed at 158–162 Ma, earlier than the porphyritic granodiorite which yields the emplacement age of 146–147 Ma. In-situ LA-ICP-MS U-Pb dating of cassiterite from the deformed skarn ores indicates the early-stage mineralization occurred at 146 ∼ 148 Ma, which is similar to the emplacement age of the porphyritic granodiorite, but earlier than the formation of quartz-cassiterite-sulfide veins and the fine-grained granite (141∼144 Ma). Further, the whole-rock and biotite geochemistry, and zircon Hf isotope compositions suggest that the porphyritic granodiorite exhibits a lower degree of magma differentiation, higher oxygen fugacity, higher Cl and lower F contents than the fine-grained granite. The porphyritic granodiorite might provide the most Cu-Pb-Zn budget accompanied by minor Sn for early-stage mineralization. Overall, our study suggests that the Jinkeng Sn-Cu polymetallic deposit formed in two scenarios where the early dominated Cu-Pb-Zn and minor Sn mineralization related to the emplacement of the porphyritic granodiorite is superimposed by the late vein-type Sn-dominated mineralization related to the emplacement of the fine-grained granite. The two isolated mineralizing events (∼147 Ma and ∼141 Ma, respectively) in Jinkeng were probably responded to the regional magmatic activities triggered by the tectonic transformation where two extensional tectonic events were separated by a short contractional event (147–144 Ma).

Vanadium isotope records of the transformation from carbonated melt to alkali basalt

Volcanic clasts from the International Ocean Discovery Program Site U1431 in the South China Sea (SCS) were analyzed for V isotopic compositions in this study. These volcanic clasts represent mantle-derived carbonated melts and record the transition from carbonated melts to alkali basalts. Based on the formation sequence, these clast samples were divided into early-stage (> 8.3 Ma) and late-stage (< 8.3 Ma) clasts. The early-stage volcanic clasts have δ51V values of −0.76‰ to −0.67‰, which provide an estimate for the V isotopic composition of primary carbonated melts. Their V isotopic compositions are slightly heavier than those of mid-ocean ridge basalts (−0.84‰ ± 0.10‰) and bulk silicate Earth (−0.86‰ to −0.91‰), reflecting the control of low-degree partial melting under conditions of high oxygen fugacity. The late-stage volcanic clasts have δ51V values ranging from −0.62‰ to 0.29‰, which are systematically heavier than those of early-stage volcanic clasts. The carbonated melts rose through and reacted with the lithospheric mantle and were transformed into alkali basalts by dissolving orthopyroxene and precipitating olivine and/or clinopyroxene. Because the reactants and reaction products do not lead to significant V isotope fractionation, the V isotopes show limited variations during transformation from carbonated melts to alkali basalts. The alkali basalts were emplaced into shallow crust by multiple pulses, in which the magma experienced variable degrees of magma differentiation, with δ51V values close to those of the initial alkali basalts or increasing due to fractional crystallization of FeTi oxides. The change in V isotopic compositions from early-stage volcanic clasts to late-stage volcanic clasts was driven by the varying magnitude of influence exerted by different magmatic processes en route from the deep mantle to the shallow crust.

Geochronology, Petrogenesis, and Metallogenic Implications of Quartz Monzonite Porphyry in the Shanlixu Copper–Gold Deposit in the Lujiang–Chuzhou Area, Middle–Lower Yangtze River Valley Metallogenic Belt, China

The Lujiang–Chuzhou Metallogenic Area is an important component of the Middle–Lower Yangtze River Valley Metallogenic Belt. Despite being an important copper–gold deposit in this area, the Shanlixu skarn Cu-Au deposit has not yet been systematically studied. According to LA-ICP-MS zircon U-Pb dating, the quartz monzonite porphyry from the Shanlixu deposit is aged 137.5 ± 1.7 Ma: while it differs from the timing of the magmatism and related mineralization in the Lujiang–Chuzhou Area, it is consistent with magmatic activity elsewhere in the Middle–Lower Yangtze River Valley Metallogenic Belt. The Ce4+/Ce3+ values of zircon in the quartz monzonite porphyry vary from 204.5 to 886.5, indicating that the intrusion might have formed in an environment with high oxygen fugacity. Additionally, the quartz monzonite porphyry exhibits high contents of Al2O3, Sr, Ba, and Mg# (Mg# = Mg2+/(Mg2+ + Fe2+)) and low ratios of Y, Nb, Ta, and K2O/Na2O, showing geochemical characteristics similar to those of adakitic rocks. Based on these characteristics, it is suggested that the intrusion might have been derived from the partial melting of subducted oceanic crust under a continental arc margin setting. Furthermore, it is strongly indicated that the quartz monzonite porphyry from the Shanlixu deposit, in the Lujiang–Chuzhou Area, is closely related to Cu-Au mineralization, as suggested by the age of the intrusion, which is approximately 137 Ma. These findings provide a new direction for research and exploration in this region.

Melting at the base of a terrestrial magma ocean controlled by oxygen fugacity

Heat delivered from accretionary impacts is thought to have led to extensive melting of early Earth’s silicate mantle, resulting in a deep magma ocean covering the surface. The mantle’s oxygen fugacity is thought to have increased over accretion and core formation due to increasingly oxidated impactors and lower mantle self-oxidation, but the influence of this on the solidus of deep primitive mantle materials has not been well constrained. Here we assess the effect of oxygen fugacity on conditions at the bottom of a magma ocean by experimentally determining the solidus of mantle pyrolite at pressures of 16–26 GPa at high oxygen fugacities. We find that over this pressure range, the solidus in experiments conducted under oxidizing conditions is at least 230–450 °C lower than in experiments conducted under more reducing conditions. Assuming constant magma ocean temperature, this would imply a magma ocean floor that deepens by about 60 km for each log unit increase in mantle oxygen fugacity. The strong influence of oxygen fugacity on mantle melting suggests that models of early Earth thermal evolution and geochemical models of core formation should be reassessed.

Mineral chemistry of chrome-diopside bearing lamprophyre from Mesoproterozoic Settupalle igneous complex of Prakasam alkaline province: insights on the magma dynamics at shallow lithospheric mantle beneath the NE margin of the Cuddapah basin, Southern India

The Eastern Dharwar Craton shows considerable variations in the activity of kimberlite, lamproite and lamprophyre and their related lithospheric thickness, thermal structure and magmatic source characteristics from the innermost core to the margin. These variations have been revealed through seismic studies and the analysis of xenoliths, and xenocrysts carried in alkaline magmas, particularly kimberlites. This study reports the occurrence of chrome-diopside phenocrysts from a lamprophyre of the Settupalle pluton, located on the northeastern margin of the Cuddapah basin, Prakasam alkaline province in South India. Studied lamprophyre are characterized by phenocrystic clinopyroxene (Cpx) and biotite, embedded in a groundmass of amphibole, biotite, opaques, calcite, feldspar, nepheline and sodalite, with the latter minerals forming ocellar structures. Clinopyroxene displays normal zoning, with a high Mg–Cr rich diopside core (up to 1.92 wt%) and a Na 2 O-, Al 2 O 3 , FeO and TiO 2 -enriched salite rim. These chemical variations, along with elemental substitutions from core to rim, indicate the significant role of fractionation in the evolution of lamprophyre magma. The lack of chemical disparity among the studied Cpx suggests closed system fractionation, under high oxygen fugacity conditions. Thermobarometry results indicate polybaric crystallization for the Cpx (1206–1269°C, 11.82–18.04 kbar) and biotite (825–856°C, 3.49–6.94 kbar). The gradient inferred from the pressure of the Cpx suggests that its crystallization occurred at a depth of 43–66 km, implying shallow lithospheric magma contribution for the genesis of the lamprophyre magma.

Copper migration and enrichment in the mantle wedge: Insights from orogenic peridotites and pyroxenites

The refertilized mantle wedge is an important source of ore-forming metals in subduction-related Cu–Au deposits. However, the source and migration of Cu in the mantle wedge are poorly constrained. Here, we present a combined study of the Cu elemental and isotopic compositions (δ65Cu) as well as Fe3+/∑Fe ratios on a well-characterized suite of the Mg-lherzolites, Fe-rich peridotites and pyroxenites from the Bohemian Massif in a Variscan subduction zone. The Mg-lherzolites represent melting residues moderately affected by metasomatism of slab-derived melts/fluids. The Fe-rich peridotites and pyroxenites are, respectively, results of Mg-lherzolite-melt reaction and crystalline products of evolved melts in the lithospheric mantle.The peridotites and pyroxenites display higher Fe3+/∑Fe ratios (0.14–0.56) than the cratonic peridotites and mid-ocean ridge basalts, indicating that the mantle wedge was oxidized by slab-derived components. The Mg-lherzolites have relatively low Cu contents (7.35–39.6 μg/g) and normal mantle-like δ65Cu values (−0.13 to 0.26 ‰), suggesting an insignificant slab-to-mantle wedge Cu transfer. In contrast, the Fe-rich peridotites and pyroxenites have variable but overall high Cu contents (37.0–513 μg/g) and heavier δ65Cu values (up to 0.83 ‰). These signatures are ascribed to secondary sulfide precipitation from the evolved Cu- and 65Cu-enriched melts, which were produced by reaction of Mg-lherzolites with subduction-related oxidative SiO2‐undersaturated basaltic melts. Such melt-peridotite reaction at high oxygen fugacity can cause the partial oxidative decomposition of primary sulfides in peridotites with the preferential release of 65Cu into the evolved melts. Our results thus demonstrate that oxidative melt-rock reaction can result in the Cu migration, redistribution and its local enrichment in the mantle wedge, which may serve as an important source of Cu for subduction-related porphyry copper deposits.

Mineral chemistry and garnet U-Pb dating in the Bizmişen iron skarn deposit, Erzincan, East-Central Türkiye

In Bizmişen area, Middle Eocene (46.3–42.0 Ma) plutonic rocks (quartz diorite) were intruded into Triassic-Cretaceous limestones and Upper Cretaceous ophiolites and caused to skarn zones containing prograde (garnet, clinopyroxene) and retrograde (amphibole, epidote, calcite, magnetite, phlogopite, serpentinite and chlorite) minerals. Due to contact relationships of quartz diorites with both serpentinized ultramafic rocks and limestone blocks, the mineralogical associations represent calcic (grossular/andradite, amphibole, chlorite and epidote) as well as magnesian (diopside, serpentine, phlogopite, talc) skarns. During the skarnization process, garnet, diopside, epidote, scapolite and amphibole minerals developed in the endoskarn zone within quartz-diorite, and diopside, tremolite, serpentine, phlogopite, talc, Mg-chlorite and calcite minerals developed in the exoskarn zones in ophiolites (serpantinite and listwaenite) and limestones. Skarn and magmatic clinopyroxenes in serpentinized ultramafic hosted exoskarn zone have a compositional range of Wo45-53En35-53Fs0–15 and Wo24-51En38-76Fs0–11, and classified as diopside and augite, respectively. The end members of garnets are Adr46–54Grs43–50Prp1–2Sps1.1–5 in amphibole-epidote-calcite-garnet skarn in endoskarn zone, whereas Adr40–93Grs4–57Prp0.2–2.3Sps0.9–2 in epidote-calcite-garnet skarn in exoskarn zone, and classified as andradite-rich grandite garnets. FeO, MnO and partially MgO contents gradually increase from the edges to the center in zoned garnet grains. Amphibole compositions represent to calcic (Ca >1 atoms per formula unit) group (pargasite) and indicate the high oxygen fugacity conditions which caused the increase in the rate of magnetite crystallization. Al2O3 and FeO contents of epidotes range 23.68–27.63 and 9.10–14.45 wt%, respectively, correspond to composition of epidote and clinozoisite. The iron oxide contents (FeO, wt%) of magnetites change from 91.72 to 98.36 correspond to structural Fe3+1.88–1.97 and Fe2+0.91–1.0 values. The contents of Ti, divalent and trivalent metal cations correspond to ulvospinel-magnetite compositional line at the magnetite end-member. The mineral chemistry of skarn minerals shows similarities to those of most iron skarn deposits. Garnet U-Pb ages (46.95–45.63 Ma) are consistent with the cooling ages of the Bizmişen pluton. The prograde stage of skarn should be occurred syn-intrusion, whereas retrograde stage should be developed later than youngest garnet age (45.6 Ma) and before the oldest late stage argillic alteration (37.5 Ma).

Mineralogy and Geochemistry of Titaniferous Iron Ores in El-Baroud Layered Gabbros: Fe-Ti Ore Genesis and Tectono-Metallogenetic Setting

The Neoproterozoic pyroxene gabbros and gabbronorites in the El-Baroud mafic intrusion in the Northern Eastern Desert (NED) of Egypt host Fe-Ti oxide ore deposits. This study discusses the major and trace elements of both titaniferous iron ores and their host rocks, along with the mineral chemistry (major and in situ trace elements) of interstitial clinopyroxene (Cpx), to gain a deeper understanding of the Fe-Ti oxide genesis. These ores occur as disseminated (55–60 vol.% of Fe-Ti oxides) and massive types (85–95 vol.%) in the form of the dyke, layer, and lens. They are composed of titanomagnetite (80–87 vol.%) with subordinate ilmenite (10–15 vol.%) and magnetite (3–5 vol.%), in accordance with their high Fe2O3 (75.66 wt.% on average) and TiO2 contents (16.30–17.60 wt.%). The Cpx in the investigated ores is diopside composition (Mg#; 0.72–0.83) and exhibits a nearly convex upward REE pattern, similar to Cpxs in the ferropicrite that originated from the primitive mantle. Melts in equilibrium with this Cpx resemble Greenstone ferropicrite melts; the parent melt of El-Baroud gabbros is possibly a ferropicritic melt that was derived from the lithospheric mantle during plume interaction. The El-Baroud gabbroic rocks were generated during the arc rifting and crystallized under a high oxygen fugacity at a temperature of 800–1000 °C and a pressure of 3 kbar with a depth of 12 km. The Fe-Ti oxide ores have been formed from ferropicritic parent melts by two processes, including in situ crystallization that leads to the formation of disseminated Fe-Ti oxides in the iron-rich gabbros at the bottom and liquid immiscibility that is responsible for the formation of thick Fe-Ti ore lenses and layers at the top of the gabbroic intrusion. Initially, titanomagnetite crystallized from the primary Ti-rich oxide melt. As cooling progressed, some of the excess titanium in this melt was exsolved in the form of the exsolution ilmenite lamellae within the titanomagnetite. The Fe-Ti oxide layers in the NED follow the trend of NW-SE (Najd trend), where their distribution is possibly controlled by the composition of parent melts (rich in Ti and Fe), high oxygen fugacity, and the structure related to the Najd fault system. The distribution of Fe-Ti oxide ores increases from the NED to the Southern Eastern Desert (SED), suggesting the dominant mantle plumes and/or shear zones in the SED relative to the NED.

Petrogenesis of the Dalaku’an Mafic–Ultramafic Intrusion in the East Kunlun, Xinjiang: Constraints from the Mineralogy of Amphiboles

The Dalaku’an mafic–ultramafic intrusion, located in the western segment of the East Kunlun, presents conducive conditions for the magmatic Cu-Ni sulfide deposits. According to the detailed petrographic observation, the amphiboles within distinct rock types were analyzed by EPMA analysis. The crystallization conditions, such as temperature, pressure, oxygen fugacity, and water content of the magma, were calculated to explore the genesis of the intrusion. The amphiboles were divided into three types: Amp-I, characterized by low silicon content but enrichment of aluminum, titanium, and alkali, predominantly comprising Tschermakitic hornblende and Magnesio-hornblende with mantle-derived traits; Amp-II, exhibiting elevated silicon content but diminished levels of aluminum, titanium, and alkali, primarily constituted of Magnesio-hornblende; whereas Amp-III manifests as Actinolitic hornblende, indicative of crustal origins. The calculated temperatures of amphiboles ranged between Amp-I (955–880) °C, Amp-II (852–774) °C, and Amp-III (761–760) °C; the pressures ranged between Amp-I (454–274) MPa, Amp-II (194–93) MPa, and Amp-III (101–84) MPa; the oxygen fugacities (△NNO) ranged between Amp-I (0.93–2.17), Amp-II (1.55–2.52), and Amp-III (1.89); and the water contents (H2Omelt) ranged from (6.69–8.67) to (5.90–7.32). The magma experienced multiple stages of crystallization and underwent complex magma evolution at different depths. The high oxygen fugacity and water content could be attributed to the subduction of the oceanic crust. The magma source of the Dalaku’an intrusion was metasomatized by fluids from subducting plates, thereby originating within a post-collision extension.

Geochronology and petrogenesis of multiple magmatic events in the Tianbaoshan orefield, NE China: Implications for tectonic evolution

Recent studies have shown that multistage magmatic and metallogenic events in NE China were dominated by the Paleo-Asian Ocean tectonic regime and the Paleo-Pacific Ocean tectonic regime. However, outstanding questions remain on the petrogenesis and fertility of ore-causative magma in each metallogenic event. In this study, we report new geochronologic and geochemical data on ore-causative intrusions from the Tianbaoshan orefield in the east Jilin-Heilongjiang belt (EJHB), aiming to identify their petrogenesis, magma fertility, and their implications for the geodynamic evolution of the EJHB. Middle Permian Lishan ore-causative quartz monzodiorites with abundant mafic microgranular enclaves (MMEs) were emplaced at ca. 264.9 ± 2.6 Ma. Petrographic and geochemical characteristics (87Sr/86Sr(i) = 0.7049–0.7053, εNd(t) = 2.9–3.7, and εHf(t) = 4.7–11.7) indicate a juvenile crust source injected by a slab-metasomatized mantle component. The Early Jurassic Beishan monzogranites (ca. 192.5 ± 1.8 Ma) were generated by the partial melting of the juvenile underplating basaltic lower crust with subsequent fractional crystallization in response to their highly evolved geochemical features, combined with their depleted Sr-Nd-Hf isotopic signature (ISr = 0.7032–0.7037, εNd(t) = 2.8–3.3, and εHf(t) = 7.2–12.2). Based on the zircon trace element geochemistry, we infer that the Middle Permian quartz monzodiorites had a high oxygen fugacity (Ce4+/Ce3+ = 40–216), potentially generating the Pb-Zn-Cu mineralization. Early Jurassic Beishan monzogranites had a lower magmatic oxygen fugacity (Ce4+/Ce3+ = 14–106), which may account for the Mo-dominated mineralization. A combination of this study and previous results corroborates that the Tianbaoshan orefield records the superposition of different tectonic regimes during metallogenesis.

Texture and Geochemistry of Multi‐stage Hydrothermal Scheelite in the Mamupu Cu‐Au‐Mo(‐W) Deposit, Eastern Tibet: Implications for Tungsten Mineralization in the Yulong Belt

AbstractMultistage tungsten mineralization was recently discovered in the Mamupu copper‐polymetallic deposit in the southern Yulong porphyry copper belt (YPCB), Tibet. This study reports the results of cathodoluminescence, trace element and Sr isotope analyses of Mamupu scheelite samples, undertaken in order to better constrain the mechanism of W mineralization and the sources of the ore‐forming fluids. Three different types of scheelite are identified in the Mamupu deposit: scheelite A (Sch A) mainly occurs in breccias during the prograde stage, scheelite B (Sch B) forms in the chlorite‐epidote alteration zone in the retrograde stage, while scheelite C (Sch C) occurs in distal quartz sulfide veins. The extremely high Mo content and negative Eu anomaly in Sch A represent high oxygen fugacity in the prograde stage. Compared with ore‐related porphyries, Sch A has a similar REE pattern, but with higher ΣREE, more depleted HREE and slightly lower (87Sr/86Sr)i ratios. These features suggest that Sch A is genetically related to ore‐related porphyries, but extensive interaction with carbonate surrounding rocks affects the final REE and Sr isotopic composition. Sch B shows dark (Sch B‐I) and light (Sch B‐II) domains under CL imaging. From Sch B‐I to Sch B‐II, LREEs are gradually depleted, with MREEs being gradually enriched. Sch C has the highest LREE/HREE ratio, which indicates that it inherited the geochemical characteristics of fluids after the precipitation of HREE‐rich minerals, such as diopside and garnet, in the early prograde stage. The Mo content in Sch B and Sch C gradually decreased, indicating that the oxygen fugacity of the fluids changed from oxidative in the early stages to reductive in the later, the turbulent Eu anomaly in Sch B and Sch C indicating that the Eu anomaly in the Mamupu scheelite is not solely controlled by oxygen fugacity. The extensive interaction of magmatic‐hydrothermal fluids and carbonate provides the necessary Ca2+ for the precipitation of scheelite in the Mamupu deposit.

Magmatic and hydrothermal evolution of the superlarge Dashui goldfield in the West Qinling Orogen, China

Gold (Au) is a precious metal that has played an important role in the development of the global economy. It is therefore important to better define the genesis of Au mineralisation as an aid to focus exploration as the consumption of Au increases. The Dashui goldfield contains a super large Au resource of over 120 t (tonnes) in the West Qinling Orogen, central China. Despite several studies have focused on the genesis of the Dashui goldfield, the original physico–chemical natures of magmatic and hydrothermal evolution remain unclear. Biotite and apatite in the mineralised diorite porphyry of the goldfield are sensitive to the changes in the physico–chemical conditions and the evolution of magmatic and hydrothermal fluids, and thus provide important keys to address these issues. Hence, we conducted detailed in–situ major and trace element studies of biotite and apatite from the ore–bearing diorite porphyry in the Dashui goldfield. Our aim is to elucidate the physico–chemical conditions, magma source, and magmatic and hydrothermal evolution processes during the deposition of the gold, and to enhance the understanding of the Au genesis in the West Qinling Au province. Using the geochemistry of magmatic apatite, and magmatic and hydrothermal biotite, we have found that the crystallisation temperature and pressure along with emplacement depth of diorite porphyry were constrained at ∼ 737–791 °C, 1.08–1.73 kbar, and 3.94–6.30 km. The diorite porphyry has the geochemical affinities with calcium alkaline orogenic suites derived from a mixed crustal and mantle source. During the early emplacement of diorite porphyry, the melt had a high oxygen fugacity and was highly enriched in Au. During the late magma crystallisation of diorite porphyry, the magma was enriched continuously in most elements with the Ba/Rb ratios in the biotite varying from 10 to 5, and most of the Au was hosted by pyrite. Additionally, elements were continuously dissolved into fluids generating Cl–rich hydrothermal fluids during the evolution of the magma. During hydrothermal evolution, Au is migrated with As and Sb in the vapour phases of fluids, whereas Au migrated with Cl in the liquid phase. When temperatures dropped to ∼ 200–400 °C, Au started to combine with S and Si in the liquid phase of fluids. Subsequently, hydrothermal fluids interacted with host carbonate to form the Dashui goldfield, Au during this stage was also transported and hosted in magnetite, hematite, and quartz within the carbonate rocks.

A-type tonian granite in the northwest of the gavião block: Record of within-plate magmatism precursor to the continental rifting of the São Francisco paleoplate?

The Early Tonian period in the São Francisco Craton represents the development of an intracontinental rift across the northern and central Espinhaço regions, playing a crucial role in understanding the tectonic evolution of the Neoproterozoic Period within this craton and its adjacent orogens. This rift is associated with the breakup of the São Francisco paleoplate, marked by the formation of several rifts, some of which were aborted (e.g. Santo Onofre Rift), and magmatism associated. Field investigations, coupled with petrographic, lithogeochemical, and U–Pb geochronological data of the Serra do Meio Suite, elucidate key characteristics and offer significant insights into the Tonian tectonic evolution of the São Francisco Craton and its relationship with Santo Onofre Rift. The suite comprises metagranitoids exhibiting a mineralogical composition spanning from alkali-feldspar granites to granites and its petrogenesis and tectonic characteristics reveal an alkaline to calc-alkalic signature, exhibiting extreme ferroan geochemistry and indications of moderate to high oxygen fugacity. Pressure estimations suggest low-pressure conditions during magma crystallization, implying shallow crustal emplacement. The suite's evolution involves complex petrogenetic processes, likely influenced by fractional crystallization and contamination by country rocks from a quartz-feldspathic crustal source, as well as a possible contribution from juvenile tholeiitic mantle sources associated with rift environments, showcasing a signature typical of A1-type granite. The U–Pb SHRIMP age, determined as 930 ± 2 Ma (MSWD = 0.34), is interpreted as the crystallization age of the rock and allows us to connect it to the opening of the Santo Onofre-Macaúbas Rift in the São Francisco Craton.

First identification of the Early Cretaceous Suolong Cu-rich porphyry in the Geji area, central Tibet: A new clue for regional porphyry Cu exploration

The Tibetan Plateau hosts the majority of porphyry Cu deposits in China. There are two large metallogenic belts, the Gangdese and Bangong-Nujiang belts, in the Lhasa Terrane, Central Tibet. The Lhasa Terrane experienced multistage magmatic activity from the Mesozoic to Cenozoic, and the subaerial volcanic areas of the western part of the terrane are regarded as favorable targets of porphyry Cu deposits. In this paper, we describe the geology of our newly identified Early Cretaceous Suolong Cu-rich porphyry in the western Lhasa Terrane and present new U–Pb ages, trace element and Hf isotopic compositions of zircon and whole-rock elemental and Sr–Nd isotopic compositions. The Suolong porphyry contains zircon grains with ages ranging from 136 to 135 Ma, εHf(t) values ranging from −1.5 ∼ +2.7 and logfO2 values ranging from −16.27 ∼ −9.92. Geochemically, the porphyry rocks are peraluminous in nature, with whole-rock εNd(t) values of −5.7 ∼ −5.4. We infer that the Suolong porphyry originated from a mixture of ∼53 % enriched lithospheric mantle and ∼47 % ancient lower crustal melt, triggered by the roll-back of the northward-subducting Neo-Tethyan Ocean. The conditions of high oxygen fugacity and water content and tectonic transition promoted the formation of the Suolong Cu-rich porphyry, but the condition of a thinned crust may have constrained the mineralization scale of the Cu deposits. This new identification of Early Cretaceous mineralization event provides important clues for identifying new potential exploration targets for porphyry Cu deposits in the western segment of the Lhasa Terrane.