Eu Anomalies Research Articles

Jurassic magmatism in the Garzón region of the Colombian Andes: insights from whole-rock geochemistry and zircon isotope analysis of granites and subvolcanic rocks

ABSTRACT New whole-rock geochemical and zircon U – Pb dating and Lu – Hf isotope data are presented for the Garzón granites and related subvolcanic rocks, which formed during widespread Jurassic arc magmatism in the Colombian Andes. This magmatism resulted from the subduction of a proto-Pacific plate under the NW South American margin. Our data indicate that the granitic and related rocks of the Algeciras, Altamira, and Sombrerillo Plutonic Massifs in the Garzón region have crystallization ages ranging from 179 to 169 Ma. These rocks are characterized as high-K alkali-calcic or calc-alkaline, magnesian, with 0.66 ≤ Fe# ≤ 0.94, and metaluminous to slightly peraluminous, with 0.67 ≤ ASI ≤ 1.01, exhibiting geochemical signatures. The trace element patterns normalized to MORB reveal pronounced negative anomalies for Nb, P, and Ti, alongside positive anomalies for Pb, Rb, Sr, Y, Zr, and Ba. The REE patterns display strong LREE fractionation over HREEs, with moderate to absent negative Eu anomalies in mafic to intermediate rocks (0.5 ≤ Eu/Eu* ≤ 1.0) and greater significance in felsic rocks (Eu/Eu* up to 0.6). Most granitic rocks display negative εHf(t)-in-zircon values (−7.7 to −1.2), indicating substantial contributions from ancient continental crust. In contrast, the subvolcanic rocks have a mix of positive and negative εHf(t) values (from −7.9 to + 11.5), reflecting significant input from both juvenile mantle and ancient crustal sources (221 Ma ≤ TDM ≤1516 Ma). After 167 Ma, the magmatic activity diminished and ceased in the Garzón region, while it continued to the west in the Central Cordillera until ca. 129–110 Ma, with a gradual increase in contributions from the mantle, as indicated by systematic zircon Hf isotopes, arguably due to changes in the subduction regimes.

Mineral Chemistry and In Situ LA-ICP-MS Titanite U-Pb Geochronology of the Changba-Lijiagou Giant Pb-Zn Deposit, Western Qinling Orogen: Implications for a Distal Skarn Ore Formation

The giant Changba-Lijiagou (Ch-L) Pb-Zn deposit is in the northeast part of the Xicheng ore cluster, Western Qinling Orogen. The ore genesis remains controversial; it could be either a sedimentary exhalative genetic type or an epigenetic hydrothermal genetic type. Here, in situ titanite U-Pb dating for the two kinds of titanite is presented, yielding ages of 212.8 ± 3.0 Ma in the mineralized skarn ore and 214.6 ± 5.1 Ma in the host rock. These ages conform to the previously reported magmatic zircon age (229–211 Ma) based on the in situ zircon U-Pb dating of plutons in this district and the time of large-scale magmatic–hydrothermal activities in Western Qinling Orogen (229–209 Ma). Titanites occurring in mineralized skarn and those that are calcite-hosted are similar to hydrothermal-origin titanites in major element characteristics. The Eu anomalies in the two types of titanite record oxidizing conditions during the mineralization process. A mineral assemblage of garnet, pyroxene, riebeckite, biotite, and potash feldspar, replacing the albite, is well-developed in the deposit. The mineralogical and geochronological characteristics indicate that the Ch-L Pb-Zn deposit is a distal skarn deposit and the result of intensive tectonomagmatic processes in the Xicheng ore cluster during the process of the Late Triassic orogeny.

The Subduction-Related Metavolcanic Rocks of Maroua, Northern Cameroon: New Insights into a Neoproterozoic Continental Arc Along the Northern Margin of the Central African Fold Belt

The metavolcanic rocks around Maroua in the Far North Region of Cameroon are located at the northern margin of the Central African Fold Belt (CAFB) and have not been studied to date. The petrographic and whole-rock geochemical data presented in this paper highlight their magma genesis and geodynamic evolution. The lavas are characterized by basaltic, andesitic, and dacitic compositions and belong to the calc-alkaline medium-K and low-K tholeiite series. The mafic samples are essentially magnesian, while the felsic samples are ferroan. On a chondrite-normalized REE diagram, mafic and felsic rocks display fractionated patterns, with light REE enrichment and heavy REE depletion (LaN/YbN = 1.41–5.38). The felsic samples display a negative Eu anomaly (Eu/Eu* = 0.59–0.87), while the mafic lavas are characterized by a positive Eu anomaly (Eu/Eu* = 1.03–1.35) or an absence thereof. On a primitive mantle-normalized trace element diagram, the majority of the samples exhibit negative Ti and Nb–Ta anomalies (0.08–0.9 and 0.54–0.74, respectively). These characteristic features exhibited by the metavolcanic rocks of Maroua are similar to those of subduction-zone melts. This subduction would have taken place after the convergence between the Congo craton (Adamawa-Yadé domain) and the Saharan craton (Western Cameroonian domain). Petrological modelling using major and trace elements suggests a derivation of the Maroua volcanics from primitive parental melts generated by the 5–10% partial melting of a source containing garnet peridotite, probably generated during the interaction between the subducted continental crust and the lithospheric mantle and evolved chemically through fractional crystallization and assimilation.

Rare earth element patterns in sediments from the Great Lakes basin

This study presents a comprehensive analysis of rare earth element (REE) concentrations in >100 sediment samples from Lakes Erie and Huron, two of the North American Great Lakes. Significant intra- and inter-lake variability in REE concentrations is observed for both lakes Erie and Huron (<10 μg/g < versus <6 mg/g ƩREE, respectively). Light (L) REE were enriched over heavy (H) REE in surface sediment samples across both lakes, particularly in the North Channel of Lake Huron. Sediment cores from both lakes contained REE concentrations that are equally variable over time and correlated with major elements and other trace metals, reflective of the strong control of sediment accumulation rates on REE concentrations. Sequential extractions show that REE are predominantly associated with the residual (silicate) fraction (>50%) and likely originated from geogenic sources (basin weathering). However, considerable REE fractions (up to 16%) were also associated with oxide, phosphate minerals and organic/reducible material, particularly for the LREE. We attribute this apportionment and LREE enrichment to aqueous complexation and export from the water column. Finally, REE normalization and pattern-fitting reveal positive Ce anomalies (up to 16.2) in specific locations that could be indicative of hypolimnic redox gradients, whereas minor Gd and Eu anomalies (0.9 for Eu, and 1.02 for Gd, on average) likely relate to the parent rock signature. Our findings contribute valuable baseline data and insights into the complex interplay of geological, hydrodynamic, and environmental factors influencing REE distribution patterns in these lake sediments.

Underplating-induced trans-crustal melting and maturation of Neoarchean continental crust in the North China Craton

A global change in granitoid compositions from early predominantly sodic tonalite-trondhjemite-granodiorites (TTGs) to later TTGs and more potassic granites occurred during the late Archean, coupled with a major period of crustal maturation. However, the detailed relationship between granitoid chemical evolution and the maturing crustal process remains enigmatic. Successive granitoid magmatism including late Neoarchean TTGs and high-K granites occurred in the Western Shandong Province granite-greenstone belt (WSP) of the North China Craton and thus preserves crucial clues of the crustal maturation process. In this study, petrology, whole-rock geochemistry, and zircon U-Pb and Lu-Hf isotopes are reported for the late Neoarchean TTG gneisses, monzogranites, and minor metabasaltic to andesitic rocks from the WSP. The ca. 2560−2540 Ma TTG gneisses show low MgO, K2O/Na2O, but high (La/Yb)N, Sr/Y, and absence of Eu anomalies, indicating their derivation from partial melting of the thickened lower mafic crust. The ca. 2530−2500 Ma monzogranites are characterized by systematically high SiO2 and K2O/Na2O, but low MgO and Sr/Y, and moderately negative Eu anomalies, revealing they were formed by intracrustal reworking of local TTGs and sedimentary rocks in the middle to upper crust. Geochemical variations of these crustal-derived granitoids suggest that they were formed by melting at gradually higher crustal levels with the melt zone moved gradationally from the eclogite stability field into the plagioclase stability field. The ca. 2530−2500 Ma calc-alkaline metabasaltic to andesitic rocks sourced from metasomatized mantle outline roles of mantle-derived magma underplating in contributions of heating and trans-crustal melting magmatism. The long-term melting processes facilitated the upward movement of volatiles and heat-producing elements from deep to shallow crustal levels, and introduced K-enriched monzogranites into the upper crust, leaving a refractory, strengthening, and tectonically stable lower crust. Secular compositional evolution of crustal-derived granitoids reveals that continuous crustal reworking drove lithosphere differentiation and paved the way for the maturation of the Archean continental crust.

Rodingitization of Neoproterozoic Al-Barramiya ophiolite metagabbro in the Eastern Desert of Egypt, Arabian-Nubian Shield

ABSTRACT The present work studies the rodingite that is recorded for the first time as being associated to Al-Barramiya Neoproterozoic ophiolite at Eastern Desert of Egypt, Arabian-Nubian Shield (ANS). Al-Barramiya ophiolite is one of the most important ophiolitic sequences exposed in the ANS. It is affected by different styles of alterations included carbonatization, listvenitization, chloritization and rodingitization. The Neoproterozoic ophiolitic rocks of Al-Barramiya district consists of serpentinized peridotite and metagabbros. Serpentinized peridotites are highly altered to assemblages of talc-carbonate rocks, listvenite and magnesite, while metagabbro is partly converted into rodingite. The field studies indicate that serpentinite and rodingite in Al-Barramiya area display high-strain cataclastic deformation. Rodingite consists of garnet, diopside, vesuvianite and chlorite with minor epidote, prehnite, actinolite and opaque minerals. The garnets and vesuvianite are mostly concentrated near the peripheries of the studied rodingite masses, while clinopyroxene, chlorite, epidote and prehnite gradually increase inwards due to progressive decreasing water/rock ratio as fluids originally buffered by serpentinite move towards equilibrium with gabbroic bulk chemistry. Some rodingite samples preserve a few relics of igneous textures of ophiolitic metagabbros. Garnets are distinguished into andradite, hydroandradite and grossular. Pyroxene is represented mainly by secondary clinopyroxene beside primary fresh relics of diopside; the latter has high Mg# (0.92–0.97) similar to ophiolitic clinopyroxene in the ANS. Rodingite is enriched in CaO, Fe2O3 and MgO but depleted in SiO2, Al2O3 and Na2O compared to associated metagabbro. The association of rodingite with serpentinites and metagabbros suggests that Al-Barramiya rodingite is genetically related to serpentinization of ultramafic rocks. The rodingitization occurred during ocean floor alteration contemporaneous with the serpentinization process. The superposition of cataclastic deformation on the altered rocks indicates that alteration preceded obduction and occurred on the seafloor of the suprasubduction zone where Al-Barramiya ophiolite was originally emplaced. During serpentinization the olivine in the peridotite broke down and released Mg2+ in the metasomatic fluids and clinopyroxene broke down producing Ca-rich fluids. These fluids react with the mafic protoliths and enrich them in MgO and CaO. Also, serpentinization fluids react with the plagioclase of the metagabbro, releasing Ca from the mafic source and concentrated it in the rodingitized samples. The positive Eu anomalies beside high Sr contents of the rodingite can be inherited from a plagioclase-rich protolith such as ophiolitic metagabbro. The enrichment of rodingite in Th and U indicates two distinct solutions affected the gabbroic protolith because the alteration of depleted peridotite to serpentinite cannot be an efficient source to enrich these elements. The present study indicates that the rodingitization process underwent lower greenschist facies conditions associating metamorphism that caused serpentinization and released Ca-rich metasomatic fluids.

Late Ordovician Bentonites From the Southern Ordos Basin: Response to the Subduction of the Proto‐Tethys Ocean

ABSTRACTThe connection between the Ordovician bentonites on the southern margin of the Ordos Basin and the Early Palaeozoic volcanic rocks of the North Qinling Orogenic Belt is crucial for understanding the subduction and collisional closure of the Shangdan Ocean during the Early Palaeozoic. This paper investigates zircon U–Pb ages, geochemistry and Lu–Hf isotopic compositions of zircons in the Upper Ordovician Zhaolaoyu Formation bentonites located on the southern margin of the Ordos Basin. U–Pb dating of zircon indicates a coeval age of 453.3 ± 1.4 Ma (MSWD = 0.99), which represents the crystallisation age during the Late Ordovician Katian stage. The bentonites exhibit higher SiO2 (57.94–77.95 wt.%) and Al2O3 (9.21–14.33 wt.%), classifying them within the low‐potassium alkali basalt to medium‐potassium calc‐alkaline series. The parent rock of the bentonites is likely intermediate to felsic volcanic rocks. The rare earth element partitioning curves of the bentonites are right‐dipping, with a more pronounced negative Eu anomaly (δEu = 0.48–0.67). The zircons in the bentonites yield two‐stage model ages ranging from 546 to 956 Ma, along with εHf(t) values between 5.56 and 13.55. These results indicate that the bentonites are products of volcanic arc magma formed in a subduction–collision environment. The interbedded bentonites in the Upper Ordovician limestones of the southern margin of the Ordos Basin may be associated with the northward subduction of the Shangdan Oceanic crust, reflecting the subduction and consumption of the Proto‐Tethys Ocean along the southern margin of the North China Block.

Hydrothermal rutile chemistry and U-Pb age fingerprinting of the formation of the giant Nurkazgan porphyry Cu-Au deposit, Central Kazakhstan

The porphyry Cu-related intrusions commonly comprise multiple phases such as the large Nurkazgan porphyry Cu-Au deposit in Central Kazakhstan, hosted in the Karagandinsky dioritic to granitic intrusive complex. Here, SHRIMP and LA-ICP-MS zircon U-Pb dating on the multiple ore-bearing intrusions from this complex confirms a punctuated magmatic history distributed over 35 m.y., and marked by three episodic porphyry events rather than a single event, with the oldest event being the early granodiorite and quartz diorite porphyries at ca. 437–440 Ma, the second being the quartz diorite porphyry at 429.7 ± 2.1 Ma, and the last being the late granodiorite and quartz diorite porphyries at 402.8 ± 3.7 Ma and 402.0 ± 3.9 Ma, respectively. The mineralization is related to the two younger episodic intrusions of quartz diorite porphyry at ∼ 430 Ma and ∼ 402 Ma, respectively. SIMS U-Pb dating of hydrothermal, Cu-rich (up to 20.9 ppm) rutile from the breccia-type ores directly constrains the timing of porphyry mineralization at 428.9 ± 6.9 Ma, which is coincident with the emplacement age of the ∼ 430 Ma quartz diorite porphyry, and thus demonstrates this porphyry as a causative intrusion generating main-stage mineralization. This close genetic link is also supported by the chondrite-normalized REE patterns of rutile, which show remarkably similar light REE-enrichments and moderate negative Eu anomalies to those of the ∼ 430 Ma quartz diorite porphyry. A molybdenite sample obtained from the main-ore stage vein, however, has a Re-Os age of 418.6 ± 1.8 Ma, which is slightly younger than the U-Pb age determinations of rutile. This indicates that the Re-Os isotope system was disturbed by the second (post-ore) thermal event related to ∼ 402 Ma quartz diorite porphyry. In line with published data, this study suggests that the rutile U-Pb age in combination with its REE patterns can be a powerful tool to trace the causative porphyry. Moreover, the typical LREE-enriched REE patterns coupled with the high Cu anomalies, inherited from the causative porphyry and related exsolving fluids, can be as diagnostic proxies for distinguishing the porphyry Cu-related hydrothermal rutile from those formed in orogenic gold deposits. Based on these two geochemical discriminators and U-Pb ages, rutile can serve as unique fingerprints to help improve porphyry copper exploration in green field or covered terranes to complement detrital zircon fertility indicators.

MINERALOGICAL, PETROGRAPHIC AND GEOCHEMICAL EVIDENCE FOR ZIRCON FORMATION CONDITIONS WITHIN THE BURPALA MASSIF, NORTHERN BAIKAL REGION

This paper reports investigation on zircons from quartz syenite, alkaline and foid syenite, as well as metasomatic rock from the fenitization zone hosted by the Burpala massif. It is performed by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDS), cathodoluminescence (CL), laser ablation inductively coupled plasma mass spectrometry (LA ICP MS), and Raman spectroscopy. Generally, all zircons from igneous rocks show rhythmic, crystal growth zoning or sector zoning (type I) except for some zircons from alkaline syenites (type II) showing patchy zoning. They systematically contain pores or cavities. The REE patterns of magmatic zircons share similar features: e.g. depletion of LREE ((Yb/La)N up to 35000), large positive Ce (Ce/Ce* 6–427) and small negative Eu (Eu/Eu* 0.37–0.93) anomalies. Zircons crystallized from quartz syenites at 830±30 °C at the early stage of rock formation, while zircons from alkaline and foid syenites crystallized at the later stage of rock formation (680–750 °C). Meanwhile, crystallization of zircons with rhythmic zoning (type I) occurs at later magmatic stage, while the formation zircons of type II is probably related to the separation of the highly fluorinated aqueous fluid from the residual melt.Zircons from fenites have a bipyramidal habit holding a heterogeneous mosaic core and a homogeneous (or rhythmic zoning) rim. The cores of zircon show flat REE patterns without significant anomalies, while the rims are characterized by noticeable fractionation of REE ((Yb/La)N 85–615) and show a positive Ce anomaly (Ce/Ce* 4–18). The Raman spectra of the cores show a higher degree of crystallinity than the rims, and their flat REE spectra are probably related to the contamination by micro inclusions. The discordant U-Pb age of 295±3 Ma was obtained for zircon rims, which is consistent with the age of formation of igneous rocks of the Burpala massif (298–291 Ma). The latter supports the syngenetic origin of metasomatic ore mineralization with the main stage of massif formation.

New approach to constraining Cr-mineralization and forearc processes: U-Pb dating and geochemistry of titanites in chromitites of the Dun Mountain ophiolite belt (New Zealand)

Ophiolites provide important insights for understanding of subduction zones and forearc mantle-wedge geodynamics. Specifically, within the mantle section, podiform chromitites may record processes associated with development of highly depleted supra-subduction ophiolites, chromium mineralization and subsequent metasomatism. This study explores the first ever U-Pb isotope and trace-element data obtained from titanites in chromitites of the Dun Mountain ophiolite belt in New Zealand. Titanite is unusual in such geochemically depleted rocks and a low recovery rate attests to its rarity (ca. 190 grains from 100 kg of material from two chromitite samples). Results of U-Pb geochronology and geochemistry for the titanites constrain both the mid-Permian timing of chromitite crystallization (∼283 Ma) and later metasomatism (∼272 Ma). Older titanite grains are depleted in HFSE and have flat REE chondrite-normalized patterns reflecting a high-degree of partial melting in depths greater than the plagioclase stability field (>15 km). Younger titanites show enrichment in HFSE, depletion in LREE and negative Eu anomalies, revealing melt extraction at shallower depths (<15 km) that likely record refertilization of the mantle-wedge. Results highlight the potential of titanites in the acquisition of direct geochronological and geochemical constraints from rocks commonly devoid of minerals suitable for U-Pb dating.

Geochemistry and Mineralogy of Upper Paleozoic Coal in the Renjiazhuang Mining District, Northwest Ordos Basin, China: Evidence for Sediment Sources, Depositional Environment, and Elemental Occurrence

This study aims to investigate the depositional environment, sediment sources, and elemental occurrence of Upper Paleozoic coal in the Renjiazhuang Mining District, Western Ordos Basin. Furthermore, SEM-EDX, optical microscope (OM), ICP-AES, ICP-MS, and AAS were used. Compared with hard coal of the world, M3 coals were enriched in Ga, Li, Zr, Be, Ta, Hf, Nb, Pb, and Th, M5 coals were enriched in Li (CC = 10.21), Ta (CC = 6.96), Nb (CC = 6.95), Be, Sc, Ga, Hf, Th, Pb, Zr, In, and REY, while M9 coals were enriched in Li (CC = 14.79), Ta (CC = 5.41), Ga, W, Hf, Nb, Zr, Pb, and Th. In addition, minerals were mainly composed of kaolinite, dolomite, pyrite, feldspar, calcite, and quartz, locally visible minor amounts of monazite, zircon, clausthalite, chalcopyrite, iron dolomite, albite, fluorite, siderite, galena, barite, boehmite, and rutile. In addition, maceral compositions of M3 coals and M9 coals were dominated by vitrinite (up to 78.50%), while M5 coals were the main inertite (up to 76.26%), and minor amounts of liptinite. REY distribution patterns of all samples exhibited light REY enrichment and negative Eu anomalies. The geochemistry of samples (TiO2 and Al2O3, Nb/Y and Zr × 0.0001/TiO2 ratios, and REY enrichment types) indicates that the sediment sources of samples originated from felsic igneous rocks. Indicator parameters (TPI, GI, VI, GWI, V/I, Sr/Ba, Th/U, and CeN/CeN*) suggest that these coals were formed in different paleopeat swamp environments: M3 coal was formed in a lower delta plain and terrestrial (lacustrine) facies with weak oxidation and reduction, and M5 coal was formed in a terrestrial and dry forest swamp environment with weak oxidation–oxidation, while M9 coal was formed in a seawater environment of humid forest swamps and the transition from the lower delta plain to continental sedimentation with weak oxidation and reduction. Statistical methods were used to study the elemental occurrence. Moreover, Li, Ta, Hf, Nb, Zr, Pb, and Th elements were associated with aluminosilicates, and Ga occurred as silicate.

Geochronology and petrogenesis of Early Mesozoic Rb-mineralized granitic rocks from the Liuzhangshan Rb, West Qinling Orogen Belt, China

ABSTRACT The newly discovered Liuzhangshan (LZS) Rb deposit is a large granite-type deposit in the West Qinling Orogenic Belt (WQOB), spatially associated with biotite monzogranite. Previous research has focused on the geological characteristics and metallogenic conditions of the LZS Rb deposit; however, its geochronology and petrogenesis remain unclear. In this study, monazite U-Pb dating of biotite monzogranite in the LZS deposit yielded a U-Pb age of 200.8 ± 0.9 Ma via laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Combined with the age of magmatic rocks in the WQOB, we propose a potential mineralization event related to Rb around 200 Ma in the WQOB. The biotite monzogranite belongs to weakly peraluminous, high-K calc-alkaline serious, containing high SiO2, Na2O, K2O, and low FeO, MgO, CaO, and P2O5. Compared with primitive mantle and relatively unfractionated granodiorites found in the WQOB, the biotite monzogranite enriched in Rb, Th, U, and Pb, deleted in Ba, Sr, and Ti, and showed negative Eu anomalies, a high Rb/Sr ratio, and a low K/Rb ratio, an ∑REE of 31.3 ppm, an LREE/HREE ratio of 6.48, a LaN/YbN ratio of 2.59, an Mg# of 4.15, and a crystallization temperature of 760°C, the biotite monzogranite also had a high differentiation index (DI = 98.2), apparent tetrad effect (TE 1,3 = 1.12 ~ 1.15), characteristic of highly fractionated I-type granite. Monzoite from the biotite monzogranite in the LZS deposit has negative εNd(t) values ranging from −12.45 to −11.17, and TDM1 of 1569 ~ 2018 Ma, indicating that the LZS biotite monzogranite originated from the partial melting of a Mesoproterozoic ancient basement material, with a minor contribution from mantle-derived melts. Highly differentiated, low Sr and Yb contents, Sr/Yb ratios, and low crystallization temperature magma facilitated the enrichment of Rb.

Trace Element and In Situ O-Nd Isotope Signatures of Apatite from the Bilihe Porphyry Au-only Deposit: Magmatic Constraints on Au Mineralization

Abstract The magmatic controls on the formation of porphyry Au-only deposits are still poorly understood. The Bilihe deposit (&amp;gt; 30 t @ 2.7 g/t Au) located at the northern margin of the North China Craton is such an example, where apatite chemistry from a causative granodiorite intrusion constrains the physicochemical conditions and ore-forming potential of the porphyry-related magmas. Apatite can be subdivided by distinct CL intensities into early CL-bright and late CL-gray/dark sub-types both occurring in fresh (Ap-f), as well as in potassic (Ap-k) and phyllic (Ap-p) altered granodiorite. The mostly euhedral CL-bright apatite shows a homogeneous texture and is enriched in LREE and depleted in Fe, Mg, Mn, Y, and U compared to CL-gray/dark apatite, which develops patchy or oscillatory zoning. The CL-gray/dark apatite exhibits decreasing Fe and Mg contents as well as δ18O values from Ap-f to Ap-k and Ap-p due to consecutive fluid alteration during porphyry evolution, which was generally not observed in CL-bright apatite. We thus conclude that all types of CL-bright apatite but only CL-gray/dark Ap-f inherit the original magma composition. Binary O-Nd isotope mixing simulations suggest that both magmatic CL-bright apatite and CL-gray/dark Ap-f were influenced by crustal sediment assimilation. Our results further indicate that the magma parental to the Bilihe porphyry Au-only deposit was H2O-poor (&amp;lt; 2 wt.%), causing plagioclase fractionation in the absence of hornblende, as evidenced by relatively low Sr/Y (&amp;lt; 0.1) and significantly negative Eu anomalies in magmatic apatite. Pressure estimates by magmatic biotite that record the late crystallization stage yielded 48.9 ± 8.4 MPa, indicating a shallow final emplacement depth of 1.85 ± 0.32 km. The studied apatites formed under volatile-saturated from S deficient magmas at relatively reduced conditions (ΔFMQ + 0.5) compared to porphyry Cu deposits. We thus conclude that these physicochemical parameters together with the low-pressure conditions result in a fertile magmatic-hydrothermal environment for the formation of Au-only porphyry deposits.

Serpentinised Mantle Section of Neoproterozoic Ophiolite at Al‐Barramiya District, North Arabian‐Nubian Shield: Tectono‐Magmatic Evolution and Metamorphism

ABSTRACTThis research focuses on the field observations, petrography, mineral chemistry and geochemistry of the serpentinised peridotite of Al‐Barramiya ophiolitic sequence to place constraints on their magmatic history and their geodynamic evolution. Al‐Barramiya ophiolitic rocks are a dismembered ophiolite which was strongly deformed and metamorphosed under greenschist to lower amphibolite facies. They comprise a mantle section dominated by highly serpentinised peridotite with less metapyroxenite and chromitite, as well as a crustal portion represented by metagabbros. Along shear zones, the ophiolite sequence was affected by several types of alteration. Extensive carbonate alteration is common in the ultramafic section, resulted in talc carbonates, listvenites and magnesite, while rodingitisation is common in the metagabbro resulted in rodingite. Despite the extensive serpentinisation, some fresh relics of primary mantle minerals such as Cr‐spinel, olivine and pyroxenes are preserved sporadically in the serpentinised peridotite. Few Cr‐spinel crystals are sometimes surrounded by subhedral flakes of Cr‐chlorite (kämmererite) that was formed due to replacement of Cr‐spinel during later alteration or regional metamorphism. The serpentinite samples are depleted in the total REE (0.56–1.19 ppm) with slightly negative to slightly positive Eu anomalies (0.89–1.28). The fresh cores of Cr‐spinel have Cr# mostly &gt; 60, and the relics of pyroxenes and olivine are Mg‐rich suggesting that the Al‐Barramiya serpentinites are residual to high degrees of melt extraction. The estimated degrees of partial melting range between 18.2% and 20.7%. All the mineralogical and geochemical characteristics of the ultramafic section of the Al‐Barramiya ophiolites are most consistent with its formation in a fore‐arc setting.

Petrogenesis and tectonic setting of the proto-tethyan dachaidan ophiolite, North China: insights from clinopyroxene chemistry and whole-rock Sr–Nd–Pb and zircon Hf isotopes

IntroductionThe Dachaidan ophiolites outcrop within an ultrahigh-pressure metamorphic belt along the northern margin of the Qaidam Basin. However, their age, source, and tectonic setting remain still in debate.MethodIn this study, we investigated the geochemistry and geochronology of the Dachaidan ophiolitic gabbros.Results and DiscussionZircon U–Pb dating yielded a crystallization age of 510.0 ± 2.8 Ma and 510.0 ± 2.9 Ma for the gabbro. The gabbros have low SiO2 contents (47.15–50.10 wt.%) and high MgO contents (6.35–9.04 wt.%) and Mg# values (55–74). The total rare earth element (∑REE) contents are 8.35–28.07 ppm, lower than those of normal-type mid-ocean ridge basalts (MORBs), and the gabbros exhibit light REE depletion or flat REE patterns, with small positive Eu anomalies (Eu/Eu* = 1.06–1.40). Trace element patterns are depleted to enriched in Nb and Ta, similar to island arc rocks and MORB. Clinopyroxene thermobarometry indicates the parental magma of the gabbros formed by high-temperature (1,318°C–1,363°C) and medium-pressure (1.27–1.64 GPa) partial melting in a mantle wedge. The gabbros have depleted Sr–Nd–Pb-Hf isotopic compositions, with (87Sr/86Sr)i = 0.704586–0.707441, εNd(t) = 4.7–6.6, and zircon εHf(t) = 7.6–11.4. The age-corrected Pb isotope ratios of these volcanic rocks are variable, with 206Pb/204Pb(t) = 18.085–18.253, 207Pb/204Pb(t) = 15.595–15.614, and 208Pb/204Pb(t) = 37.880–38.148, which are similar to the isotopic compositions of typical Indian MORBs. The source of the Dachaidan ophiolite is inferred to have been depleted mantle. The Dachaidan ophiolite likely formed in a forearc oceanic setting along the northern margin of the Qaidam Basin, during the initial subduction of an oceanic plate.

From birth to death: The role of upper-crustal thermal maturation and volcanism in porphyry ore formation revealed in the Yerington district

The current race towards greener energy and its intertwined increase in Cu demand imposes the need to find mineralized centers that are economic despite greater depths. To this end, a better understanding of the processes controlling the metal tonnage of porphyry Cu deposits, the main source of Cu, is needed and the focus of current research and debate. This study provides a comprehensive view of the duration of upper-crustal magmatism and its significance in the degree of metal endowment in porphyry Cu deposits using the Yerington batholith, Nevada, USA, as a case study. The Yerington district constitutes an exceptional example of an exposed porphyry Cu system where the plutonic environment that fed the porphyritic dikes is accessible. Combining trace element geochemistry and high-precision geochronology of zircon from all exposed units, we propose that the thermal maturation of the upper crust by a continuum in magmatic activity without significant hiatuses is a key factor in enabling the formation of large porphyry Cu style mineralization. The Yerington magmatic system transitioned from a volcanically active environment with coeval plutonism to a growing upper-crustal magmatic reservoir that fed the porphyritic dikes and associated mineralized centers to then resume its volcanic activity terminating the ore-forming episode. A relatively high volcanic/plutonic ratio characterized the first expressions of Jurassic magmatism in the district from ∼170 Ma with the coeval eruption of the Artesia Lake volcanics and the protracted emplacement of the McLeod Hill pluton. Geochemically, this period recorded distinctive negative Eu anomalies and a gentle increase in Yb/Dy ratios in zircon with decreasing Ti contents over a large range of zircon crystallization temperatures. This persistent magmatism over ∼2 Myr thermally matured the upper crust, enabling the growth of magmatic reservoirs that formed the Bear and Luhr Hill plutons without known volcanic activity for ∼1.3 Myr. Zircon trace element compositions indicate that this transition occurred as a continuum in decreasing negative Eu anomalies and increasing Yb/Dy with decreasing Ti contents and age across the plutonic units, reaching the more evolved signatures and lowest crystallization temperatures in the zircon from porphyry dikes. An increase in the volcanic/plutonic ratio with the eruption of the Fulstone Spring sequence likely terminated the ore-forming potential of the district. Although many other studies have provided important views on the timing and duration of porphyry Cu deposit formation, the link to their plutonic roots has been limited due to their inaccessibility. Therefore, this study offers the first complete picture into the temporal and chemical evolution of an upper-crustal magmatic system and the roles that factors like prolonged magmatism and volcanism play before and after ore formation. We argue that without the thermal maturation of the upper crust, the construction of a long-lived magmatic reservoir would not have been possible, precluding the formation of porphyry Cu deposits. Under this premise, not only the duration of ore-related magmatic activity, but the occurrence of long-lived precursor magmatism might exercise crucial control on the final tonnage of the deposit and should be considered during exploration for new porphyry deposits.

Europium anomaly as a robust geogenic fingerprint for the geographical origin of aquatic products: A case study of nori (Neopyropia yezoensis) from the Japanese market

Rare earth element (REE) concentration patterns, while essential in geochemistry for tracing sample histories, have yet to be utilised entirely in food origin authentication. This research analysed 13 heavy metal(oid)s and REEs in Japanese edible seaweed Nori sheet samples (Neopyropia yezoensis), showing that the concentrations mirror the laver cultivation area's geological features (island arc-trench systems vs. continental crust). Thresholds for cadmium (0.5 ppm) and thorium (3.3 ppb) differentiate Japanese products from Korean imports. The slope of REE pattern, gadolinium anomalies, and yttrium/holmium ratios were also examined. However, nori samples significantly conveyed europium (Eu) anomalies, aligning with the mariculture hinterland's geochemistry. Both Japan's major seaweed mariculture areas, the Ariake Sea and the Seto Inland Sea, and Korean imports revealed distinct Eu anomalies (Eu/Eu* = 0.81–0.90, 0.58–0.66, 0.71–0.77), underscoring the potential of Eu anomalies as reliable seafood origin verifiers. This was also confirmed by literature values of Chinese samples.

Petrogenesis of episodic volcanic-intrusive rocks in SE China: Crystal-melt segregation and magma mixing

Crystal-melt segregation and magma mixing are key magmatic processes that generate compositional variabilities in igneous rocks. Distinguishing these processes can provide insight into the evolution of volcanic calderas and the driving force of plate subduction. Intensive episodic magmatism occurred in Southeast China during the Cretaceous, producing a series of volcanic-intrusive rocks during different magmatic stages in chain-like calderas. We conducted comprehensive petrological, geochemical, isotopic, and zircon trace element analyses on two representative calderas (Xiaoxiong and Shiniushan).The results show that the magmatism produced multistage volcanic and coexisting intrusive rocks regarding their crystallization ages (102–88 Ma) and NdHf isotopic compositions (zircon ɛHf(t) = −11.7 to −1.8, whole-rock εNd(t) = −8.3 to −2.4). The volcanic and intrusive rocks are related by fractional crystallization.In general, the erupted silicic rhyolitic rocks are characterized by distinctly negative Eu anomalies (δEu = 0.10–0.71) and depletions of Ba, Sr, P, and Ti, while the coexisting intrusive rocks show distinct or complementary geochemical signatures, such as neglectable Eu anomalies (δEu = 0.92–1.09) and positive Ba anomalies. Furthermore, the whole-rock samples from the calderas have variable δ41K values (from −0.14 ‰ to −0.59 ‰) that show strong correlations with indices of fractional crystallization such as Eu anomaly, Sr content, and K2O/Na2O ratios, indicating a key role of plagioclase during crystal-melt segregation. This is also supported by petrographic evidence for crystal accumulation such as the synneusis of plagioclase phenocrysts. Mafic microgranular enclaves in the volcanic-intrusive rocks indicate that magma recharge events occurred in the magma reservoir. Synthesizing these lines of evidence, we argue the multiple magmatism in plate subduction zone can be sustained by recharge events in the magma reservoir along with crystal-melt segregation processes. Particularly, the volcanic rocks tend to have isotopically lighter K than intrusive rocks, and strongly support that the volcanic rocks represent the extracted melt that is complementary to the cumulative intrusive rocks.

The use of combined C[sbnd]Mg isotope compositions of carbonates from orogenic Sb[sbnd]Au deposits as a tracer of fluid interaction with sea-floor altered crust

The Mesoarchaean Murchison Greenstone Belt is composed of a strongly deformed volcano-sedimentary succession metamorphosed up to amphibolite facies and surrounded by metaluminous and peraluminous granitoids in the north of the Kaapvaal Craton of southern Africa. A circa 40 km-long shear-zone of strongly carbonatised rocks (the Antimony Line, or Sb-Line) oriented along the main trend of the greenstone belt (WSW–ENE) hosts important Sb deposits with accessory Au. These commodities mostly occur as stibnite and native gold hosted by quartz‑carbonate rocks at the centre of the Sb-Line, underlining the importance of CO2-rich fluid flow for mineralisation during deformation and metamorphism.In this study, we compare the elemental and stable isotope (C-O-Mg) composition of carbonates from the Sb-Line with regionally distributed carbonates hosted by the volcano-sedimentary succession distal to mineralisation. The carbonates of the Sb-Line and regional rocks have overlapping major element compositions. Both magnesite and dolomite in most Sb-Line samples have marked light-REE-depleted patterns with variable positive Eu anomalies. Carbon isotope ratios define two clusters, with marked δ13C peaks at ca. -5 ‰ for Sb-Line rocks and ca. -2 ‰ for regional rocks, implying separate C-sources. The peak at ca. -2 ‰ likely represents early carbonatisation through sea-floor alteration, whereas the first peak at ca. -5 ‰ is indicative of deep CO2 (mantle, or magma-derived) introduced during tectonic activity of the Sb-Line. Magnesium isotope ratios of regional rocks reveal limited fractionation (bulk δ26Mg = −0.27 ± 0.10 ‰) that overlap with mantle values, but some carbonate-bearing veins present 26Mg-depleted compositions (bulk δ26Mg = −1.91 to −0.40 ‰). Sb-Line carbonated rocks have more fractionated Mg isotope compositions (bulk δ26Mg = −0.8 to 0.0 ‰) and carbonates display marked negative 26Mg values (δ26Mg from −1.46 to −0.31 ‰). We interpret these results in terms of preferential remobilisation of isotopically light Mg during fluid-rock interaction and dissolution of carbonate in the host-rocks. The lack of correlation between δ13C and δ26Mg indicates decoupling of these isotopic systems, implying contribution from isotopically distinct sources of C and Mg to the mineralised zone.Similar to other structurally controlled AuSb mineralisation in Archaean greenstone belts, metal transport and ore deposition in the Murchison Greenstone Belt was closely related to the deep cycle of carbon, linking C-draw-down during sea-floor alteration, carbonate re-mobilisation during metamorphism and CO2 degassing from deep sources along major crustal discontinuities. In contrast to models for orogenic AuSb deposits invoking a purely intra-crustal, metamorphic origin of mineralising fluids, our results underline the importance of deep-sourced fluids originating from an external source from the volcano-sedimentary succession.

New insights on the petrogenesis of the Koktokay No.3 pegmatitic dyke: Petrological and zirconological evidence from the Aral granitic complex (Xinjiang, China)

The Koktokay No.3 pegmatite dyke (KPD), containing numerous Li–Be–Nb–Ta–Cs mineral resources, is among the world’s most famous rare-metal deposits, and attracted much attention. Up to now, over thirty geochronological data have been reported ranging from 332 Ma to 120 Ma for the KPD, which causes uncertainty about the origin and petrogenesis of the pegmatite. In this contribution, whole-rock geochemistry and zircon geochronology have been conducted on the Aral biotite monzogranite (BMG), the Koktokay muscovite alkali-feldspar granite (MAG), and the KPD. Petrological and whole-rock geochemistry results reveal that the BMG is normal granite with medium SiO2 (mean of 67.23 %), enriched in compatible trace elements such as Ba, Sr and Zr, and slight negative Eu anomalies, while the MAG belongs to highly-fractionated granite with high SiO2 (mean of 73.92 %) and extensive negative Eu anomalies, and enriched in incompatible trace elements such as Rb, Ta, and U. Zircon morphology and LA–ICPMS analysis reveal that magmatic zircons from the BMG, hydrothermal zircons from the MAG and KPD yield lower intercept ages at 217.3 ± 2.4 Ma, 197.8 ± 4.7 Ma, and 195.4 ± 2.0 Ma, respectively. Combining with tectonic information and geochronological data of granitic activity and its mineralization in the Altay, this study explains the petrogenetic mechanism of the KPD after Wang et al. (2021)‘s metallogenic model: (1) In late stage of Middle Triassic, the collision between the Siberian plate and the Kazakhstan–Junggar plate caused a large number of thrust nappe faults and crust thickening in the Altay orogenic belt; At ∼217 Ma, the compression reached its peak, the crustal anatexis produced syn-collisional BMG (i.e., the Aral BMG); After the compressive peak, huge amount of granitic magma in deep-seated magma chamber underwent over 20 Myr of fractional crystallization, and the residual magma enriched in ore-forming materials (rare metal elements, volatile components, and aqueous fluids) occurred at the top of the magma chamber; (2) When the regional stress converted from compression to extension, the highly-fractionated residual magma ascended rapidly from the long-lived magma chamber along extensional faults at ∼195 Ma; The huge amount of melt-bearing fluids were exsolved from the residual magma in the course of its emplacement due to sharply decreasing pressure, and intruded into a large cavity generated by extensional fault; Along with slowly decreasing temperature, the melt-enriched fluids crystallized outside-in as (quasi-) concentric pegmatitic zones (i.e., KPD); (3) The residual magma which lost huge amount of fluid filled the lower space of the extensional system, and crystallized as post-collisional MAG (i.e., the Koktokay MAG). Based on the genetic relationship among tectonics, petrogenesis, and metallogeny, the proposed model shows material and energetic conversion processes from syn-collisional granites to post-collisional granites with granitic–pegmatitic deposits