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Owing to the paucity of research on synchronous mafic rocks in the Tarim Basin, the late Paleozoic–early Mesozoic tectonic development of this region is not well defined. The Halaqi region is situated on Tarim's northwest edge, and numerous mafic dikes can be found cross-cutting the Permian strata. The whole-rock geochemistry, zircon U–Pb age, and Sr–Nd isotopic signature of these mafic rocks have never been reported before, and this contribution can offer geochronological and petrogenetic investigations that provide fresh insight into the geodynamic development of the area. Major oxide contents in the Halaqi mafic rocks vary, including SiO2 (45.74–50.31 wt.%), Al2O3 (13.28–14.8 wt.%), FeOT (16.48–19.19 wt.%), MgO (7.58–10.32 wt.%), CaO (7.19–12.39 wt.%), Na2O (2.97–4.50 wt.%), K2O (0.24–0.63 wt.%), TiO2 (1.11–1.29 wt.%), MnO (0.14–0.16 wt.%), and P2O5 (0.13–0.17 wt.%). The mafic rocks are enriched in high-field-strength elements (e.g., Zr and Hf) and large-ion lithophile elements (e.g., Sr, Th, and U) but depleted in Nb, Ta, and P. The total REEs in the rocks are lower (ΣREE = 72.80–86.85 ppm), and HREEs are somewhat depleted in comparison to LREEs, with positive Eu anomalies (Eu/Eu* = 1.05–1.17) but weak negative Ce anomalies (Ce/Ce* = 0.91–0.93). Zircon U–Pb ages of 201–247 Ma were obtained from a total of 18 magmatic zircon grains found in the mafic rocks that were studied. These results point to a middle-to-late Triassic emplacement. The mafic dikes exhibit somewhat enriched Nd isotopic compositions (εNd(t) = –1.6~–0.2) and an older Nd model age (TDM = 1.24–1.37 Ga). The Halaqi middle–late Triassic mafic dikes are thought to have originated from the same tectonic background as the Permian Tarim Large Igneous Province, along with similar geochemical and isotopic compositions. This suggests that they are all products of the interaction between asthenospheric and lithospheric mantles in an intraplate extensional environment. Research indicates that the Triassic mafic magmatism in northwest Tarim could be the product of the continuous thermal pulse of the Tarim mantle plume and be a part of the Tarim LIP. [ABSTRACT FROM AUTHOR]

Diamondiferous kimberlites occur in the Wafangdian area in the eastern part of the North China Craton (NCC). In order to better constrain their magmatic source and emplacement time, we have investigated apatite from two kimberlites, i.e., the #110 dike kimberlite and the #50 root-zone kimberlite by measuring in situ their U–Pb and Sr–Nd isotopic compositions. The crystallization ages of the #110 and #50 apatites are 460.9 ± 16.8 Ma and 455.4 ± 19.3 Ma, respectively. For the #50 apatite, 87Sr/86Sr = 0.70453–0.70613 and εNd(t) = −2.74 to −4.52. For the #110 apatite, 87Sr/86Sr = 0.70394–0.70478 and εNd(t) = −3.46 to −5.65. Based on the similar distribution patterns of the rare earth elements (REEs) and the similar Sr-Nd isotope compositions of the apatite, it is believed that the #110 and #50 kimberlites have the same source region and the kimberlite magmas in Wafangdian were derived from an enriched mantle source (EMI). The primary magmatic composition has little effect on the emplacement pattern. It is more likely that the geological environment played an important role in controlling the retention and removal of volatile components (H2O and CO2). This led to the different evolutionary paths of the kimberlite magma in the later period, resulting in differences in the major element compositions of the apatite. High Sr concentrations may be associated with hydrothermal (H2O-rich fluid) overprinting events in the later magmatic period; the higher light rare earth element (LREE) concentration of the #50 apatite reflects the involvement of the REE3+ + SiO44− ⇔ Ca2+ + PO43− replacement mechanism. Two emplacement patterns of the #110 dike kimberlite (#110 apatite, low Sr, and high Si) and the #50 root-zone (#50 apatite, high Sr, and low Si) kimberlites were identified via major element analysis of the #110 apatite and #50 apatite. [ABSTRACT FROM AUTHOR]

During the Ediacaran–Cambrian transition, a series of stratal continuous and well-preserved siliceous rock and phosphorite assemblages developed in Qingzhen, Guizhou Province, China, facilitating research on the biological evolution, marine chemistry, and palaeoecological environment of this period. Therefore, we investigated the paleontology, trace and rare earth elements, total organic carbon, total sulfur content, and Zn isotopes of the phosphorus-bearing rock series in the Taozichong Formation of the Cambrian period in Qingzhen. Geochemical analysis reveals that the sedimentary rocks in this area were formed in the oxygen-rich seawater environment and were not affected by high-temperature hydrothermal activity. The upwelling ocean current provided abundant rare earth elements and other nutrient elements, as well as conditions for the prosperity of biota in Qingzhen. In addition, the δ66Zn value (−0.21‰–0.41‰ range and 0.17‰ mean) in the Qingzhen phosphorous rock series was much lower than that in seawater, indicating a strong level of biological productivity. The variation trend of δ13C, δ18O, and δ66Zn exhibited four stages and three obvious drift events. The results suggest that climate change during this period led to the intermittent flourishing and extinction of organisms, which triggered the negative drift of δ13C and δ18O in the ocean, resulting in a coordinated response of δ66Zn. The unique ecological environment of the Taozichong Formation in Qingzhen also provides favorable conditions for the population continuation of Ediacaran-type benthic soft-bodied metazoon dominated by discoid fossils, Shaanxilithes, worm fossils, and sponge fossils in the Cambrian strata, as well as participation in the global biological explosion events. The study area provides new insights for rebuilding the global Ediacaran–Cambrian ecosystem during the transition period. [ABSTRACT FROM AUTHOR]

Prydz Bay is an important part of the Pan-African high-grade tectonic mobile belt. The focus of this investigation, by applying zircon LA-ICP-MS U-Pb geochronology, zircon Lu-Hf isotope systematics, and whole-rock geochemistry, is on Pan-African pegmatites in the Larsemann Hills of Prydz Bay, East Antarctica, their association with country rocks, and the formation conditions. Based on the obtained results, it is concluded that the pegmatites exhibit elevated levels of silica and alkali and possess peraluminous features. These pegmatites originated during the late Neoproterozoic–Early Cambrian (Pan-African) event, specifically in the D2–D4 stages. The D2 stage occurred between 546 and 562 Ma, followed by D3-stage pegmatites around 534 Ma. The pegmatites from the D2–D3 stages are considered to originate from Paleoproterozoic crustal materials, while there are at least two phases of pegmatites in the D4 stage (~517 Ma and ~521 Ma). The D4-1 pegmatite (~521 Ma) suggested both Paleo–Mesoproterozoic crustal origin, perhaps connected to extension. The D4-2 pegmatite (~517 Ma) originated from the crust layers. In the Larsemann Hills, Pan-African pegmatites formed in a recurring regime of tension. Therefore, the obtained data elucidate that a Pan-African stretching process might have occurred in Prydz Bay. [ABSTRACT FROM AUTHOR]

Geochemical studies of rare earth elements (REEs) as well as major and trace elements were conducted on the beach placer sands from the Kanyakumari coastal region, a well-known high background natural radiation area (HBNRA). For the first time, uranium isotope ratios (234U/238U and 235U/238U) were determined in the study area to investigate the provenance and leaching of U from the beach sands. Inductively coupled plasma mass spectrometry was used for the measurement of REEs and trace elements whereas thermal ionization mass spectrometry (TIMS) was used for the measurement of U isotope ratios. ∑REEs were found to be in the range of 778.93 to 15,007. 54 µg/g, whereas ∑Light REEs were in the range of 770.58 to 14,860.80 µg/g and ∑Heavy REEs varied from 8.35 to 146.74 µg/g. The enrichment factor showed the LREEs Th and U were extremely enriched in the Kanyakumari beach placer sands. The 235U/238U isotope ratios were similar to the natural terrestrial ratio value. The 234U/238U activity ratio varied from 0.995 to 1.071, and showed the prevailing secular equilibrium among them. The δ238U results could, to some extent, explain the U fractionation and source. [ABSTRACT FROM AUTHOR]

The Xinghongpu Formation is very important for understanding the Devonian tectonic evolution of the South Qinling orogenic belt. Geochemical, detrital zircon U-Pb-Hf isotopic studies were carried out on the Late Devonian metasedimentary rocks of the Xinghongpu Formation to constrain the depositional age, the provenance, and the tectonic setting. The detrital zircon U-Pb dating results revealed that the depositional age of the Xinghongpu Formation of the Late Devonian was not earlier than 363.2 Ma. The whole-rock geochemistry suggested that (1) this suite of metasedimentary rocks was mainly derived from quartzose sediments of mature continental provenance, with a small contribution from mafic and intermediate igneous provenance, and (2) the metasedimentary sandstone of the Xinghongpu Formation from the Late Devonian was deposited in an active continental margin to continental arc setting. The detailed detrital zircon U-Pb dating showed that the age spectra of detrital zircon could be divided into four groups: (1) 416–480 Ma, accounting for about 23%; (2) 740–850 Ma, accounting for about 19%; (3) 889–1017 Ma, accounting for about 19%; and (4) 1072–1146 Ma, accounting for about 12%. It also contained a group of Early Proterozoic zircons. The age and Hf isotope of the detrital zircons suggested that the clastic sediment deposited in the Xinghongpu Formation mainly came from the South Qinling Orogenic Belt and the North Qinling Orogenic Belt. The detrital zircon Lu-Hf isotopes indicated that most zircons were the products of the ancient crustal remelting, and the mantle-derived magmatic sources contributed to the provenance. The Xinghongpu Fm. formed in an oceanic basin in a continental margin environment with arc systems. [ABSTRACT FROM AUTHOR]

This paper presents data on the geological position, geochemical features, main mineral composition (micas, feldspars), and melt and fluid inclusions in quartz from Aba high-silica leucocratic granitoids in the western part of the Talitsa batholith, Russian Altai. According to these new geochemical data, the granitoids are classified as S-type, meaning they are formed via the partial melting of metasedimentary source rocks. Geological data and oxygen isotope composition analysis indicate that major-phase granitoid magma evolution took place at the level of intrusion formation, whereas the parent melt of late-phase leucogranite evolved in a deeper chamber. The geochemical features (HFSE and REE, and REE spectra) of the granitoids indicate significantly higher differentiation in the late leucocratic phase. The presence of coexisting syngenetic melt and fluid inclusions shows that leucogranite magma was already saturated with volatiles in the early crystallization stages. Based on the new data presented in this work, the Aba rock formation is associated with the volatile saturation of magmatic melts, the exsolution of a fluid phase, and magma degassing. [ABSTRACT FROM AUTHOR]

The Jinzhuping and Changkeng granites are related to the Helong W–Sn ore field in southern Jiangxi Province, China. Three different phases can be found in the Jinzhuping pluton, and their LA-ICP-MS zircon U–Pb ages are 155.2 ± 0.68 Ma, 154.0 ± 0.56 Ma, and 153.4 ± 0.99 Ma, respectively, indicating two types of granitic rocks. All granites in the Helong ore field have similar geochemical characteristics, they have high contents of SiO2 (73.99 wt.%–77.68 wt.%), and total alkali (7.56 wt.%–8.76 wt.%) and are weakly to strongly peraluminous. They are slightly enriched in HREE and depleted in Eu, Ba, Sr, P, and Ti. Zircon εHf(t) values of the Jinzhuping three granites are from −14.4 to −10.4, from −15.3 to −11.4, and from −18.1 to −10.5, and the Hf TDM model ages range from 1.83 to 2.06 Ga, from 1.89 to 2.14 Ga, and from 1.83 to 2.31 Ga, respectively. Whole-rock geochemistry and Hf isotope analysis indicate that the Helong granites experienced a high degree of differentiation and evolution derived by partial melting of the Late Paleoproterozoic crustal materials, and they formed in a backarc caused by low-angle subduction of the Paleopacific plate. [ABSTRACT FROM AUTHOR]

The Qin-Hang Metallogenic Belt (QHMB), an important metallogenic belt in South China, hosts Cu and W–Sn polymetallic deposits. The Tongshanling ore field in the QHMB is characterized by the coexistence of Cu- and W-bearing polymetallic deposits, which are related to granodiorite and granite porphyry. This study examined whole-rock geochemistry, geochronology, and Sr–Nd–Hf isotopes to determine the genetic relationship between diverse ore-related granitoids (i.e., granodiorite and granite porphyry) and Cu–W metallogeny in the Tongshanling ore field. Zircon LA-ICP-MS U–Pb dating shows that the granodiorite and granite porphyry in the Tongshanling ore field were emplaced at 163.7 ± 0.4 Ma to 154.7 ± 0.6 Ma and 161.1 ± 0.3 Ma, respectively. Geochemically, the granodiorites are classified as oxidized I-type, while the highly evolved granite porphyry is reduced A-type. The Lu–Hf isotopic composition of the granodiorites is characterized by εHf(t) values ranging from –10.49 to –4.99 (average = –7.17), with corresponding TDMC ages ranging from 1524 to 1877 Ma (average = 1682 Ma). In contrast, the granite porphyry has higher εHf(t) values (–3.60 to –1.58, average = –2.78) and younger TDMC (1310–1438 Ma, average = 1387 Ma). The εNd(t) values of granodiorite are −8.06 to −7.37 and the two-stage model ages (TDM2) are 1543–1598 Ma, while the granite porphyry has higher εNd(t) values (−3.0 to −3.4) and younger TDM2 ages (1195–1223 Ma). The results show that the granodiorite and granite porphyry were formed from partial melting of different Mesoproterozoic basement rocks under varying degrees of crust–mantle interaction. Granite porphyry underwent well-recorded fractional crystallization. Compared to the Cu-forming granodiorite, the W-forming granite porphyry has a higher differentiation index, higher crystallization temperatures of zircon (average = 708 °C versus 631 °C), and lower oxygen fugacity (median ΔFMQ = –2.21 versus –1.77). [ABSTRACT FROM AUTHOR]

The Alxa block is located in the southwestern margin of the North China Craton. The Paleoproterozoic tectonic evolution, crustal growth and tectonic affinity of the block remain unknown or controversial. The Longshoushan (LS) area is one of the few areas that outcrop Paleoproterozoic to crystalline basement rocks in the Alxa Block. In this study, we preset whole-rock geochemistry, zircon U-Pb geochronology and Lu-Hf isotope data from metagabbro, metadiorite, quartz syenite, granitic leucosome and pegmatoid leucosome in the LS area. These rocks all are enriched in LREE and LILE, and depleted in HREE and HFSE. Eight new LA-ICP-MS zircon U-Pb ages yielded three magmatic ages of 2044 Ma, 2029 Ma and 1940 Ma, and three metamorphic ages of 1891 Ma, 1848 Ma and 1812 Ma. Lu-Hf analyses reveal that the magmatic zircons and anatectic/metamorphic zircons from all the rock types are characterized by positive eHf(t) (-0.16 to 10.89) and variable eHf(t) (-11.21 to 6.24), respectively. Based on the previous studies and our new data, we conclude that the LS area experienced three magmatic events (2.5-2.45 Ga, ~2.1-2.0 Ga and ~1.95-1.91 Ga) and three regional metamorphism/anataxis events (~1.93-1.89 Ga, ~1.86-1.84 Ga and ~1.81 Ga) in Paleoproterozoic. The age-Hf isotope data establishes two main crustal growth events at ~2.9-2.5 Ga and ~2.2-2.0 Ga in the LS area. These data indicate that the LS area experienced intraplate extensional setting in the middle Paleoproterozoic, and continental subduction, collision and exhumation in the late Paleoproterozoic. Combining the geochronological framework and tectonic evolution, we suggest that the Alxa Block is part of the Khondalite Belt. [ABSTRACT FROM AUTHOR]

The Tongkuangyu copper deposit in Zhongtiaoshan at the southern margin of the North China Craton is one of the oldest porphyry Cu deposits in the world and its metallogenesis and tectonic evolution have been debated. Here, porphyritic intrusion geochemical and geochronological data are reported to identify the diagenetic age, mineralization, tectonic setting, and evolution of the deposit. Geochemical data show that granodiorite porphyry is a peraluminous rock, with low concentrations of Fe (~3.99%) and Ti (~0.29%) and high concentrations of alkali (~6.13%) and high Al (~15.42%) and Mg numbers (~51). The rocks show comparative enrichment of Na, K, and Mg; higher La/Yb ratios, no significant Eu anomaly, and obvious Nb–Ta–Ti negative anomaly, showing similar geochemical characteristics to Archean TTG and sanukitoid. ΣREE vary greatly, ranging from 33.47 × 10−6 to 277.81 × 10−6 (average 137.09 × 10−6). The characteristics of REE show obvious fractionation of LREE and HREE, enrichment of LREE, and depletion of HREE. Some of the LREE (La and Ce) and LILE (K, Rb, and Ba) are enriched, but some of the LILE (Th and U) are depleted. In addition, some of the HFSE (Nb, Ta, P, and Ti) are depleted while some (Zr and Hf) are enriched. High precision LA–MC–ICP MS zircon U–Pb dating yield concordant ages of 2159 ± 19 Ma, which is broadly coeval with ore formation (~2.1 Ga) in the area. Zircon εHf(t) values range from −3.8 to 1.13, with a model age of 2778 to 2959 Ma, indicating that the formation of porphyry is related to the partial melting of Archean crust (~2.7 Ga) with a minor amount of mantle material added. Tongkuangyu granodiorite porphyry formed in the tectonic setting of the post-orogenic extension in the Paleoproterozoic, and Tongkuangyu Cu deposit may be related to the extension of the North China Craton in the Paleoproterozoic. [ABSTRACT FROM AUTHOR]

We present geological, bulk-rock geochemical and Sr–Nd–Hf isotopic data for mafic rocks from the West Philippine Basin (WPB). These mafic rocks comprise pillow basalts characterized by a vesicular structure. The mid-ocean ridge basalt (MORB)-normalized trace element patterns of basalts from the study area display depletions in Nb. In addition, the chondrite-normalized lanthanide patterns of basalts from the WPB are characterized by significant depletions in the light lanthanides and nearly flat Eu to Lu segments. The investigated rocks have initial 87Sr/86Sr ratios (87Sr/86Sr(i)) of 0.703339–0.703455 and high εNd(t) values (8.0 to 8.7). Furthermore, basalts from the WPB have 176Hf/177Hf ratios that range from 0.28318 to 0.28321 and high εHf(t) from 15.2 to 16.3. Semi-quantitative modeling demonstrates that the parental melts of basalts from the study area were derived by ~20% adiabatic decompression melting of a rising spinel-bearing peridotite source. The Sr–Nd–Hf isotopic compositions of basalts from the WPB indicate that their parental magmas were derived from an upper mantle reservoir possessing the so-called Indian-type isotopic anomaly. Interpretation of the isotopic data suggests that the inferred mantle source was most likely influenced by minor inputs of a sediment melt derived from a downgoing lithospheric slab. Collectively, the petrographic and geochemical characteristics of basalts from the study area are analogous to those of mafic rocks with a back-arc basin (BAB)-like affinity. As such, the petrogenesis of basalts from the WPB can be linked to upwelling of an Indian-type mantle source due to lithospheric slab subduction that was followed by back-arc spreading. [ABSTRACT FROM AUTHOR]

The paper presents new geochemical data of the basic to intermediate volcanic rocks from the Hronic unit. The studied rocks are strongly altered and the primary mineral composition (clinopyroxenes, amphiboles, spinels, biotites, and plagioclases) is preserved only in some localities. The clinopyroxene corresponds to augite and primary amphiboles to pargasites. Spinels have a chemical composition similar to spinels from volcanic rocks. According to chemical composition, the studied basalts correspond to rift-related continental tholeiites. 143Nd/144Nd vs. 87Sr/86Sr isotopic ratios of the basalts are scattered around the value of 143Nd/144Nd for CHUR, where 143Nd/144Nd ratios are relatively stable and 87Sr/86Sr values are relatively varied. According to isotopic ratio of 207Pb/204Pb vs. 206Pb/204Pb, the basalt analyses lie in the field of EMII (mantle source enriched with crustal materials). The new results of U-Pb LA-ICP-MS dating of apatite point to an age 254 ± 23 Ma (Lopingian). [ABSTRACT FROM AUTHOR]

Shikoku Basin is unique as being located within a trench-ridge-trench triple junction. Here, we report mineral compositions, major, trace-element, and Sr-Nd-Pb isotopic compositions of bulk-rocks from Sites C0012 (>18.9 Ma) and 1173 (13–15 Ma) of the Shikoku Basin. Samples from Sites C0012 and 1173 are tholeiitic in composition and display relative depletion in light rare earth elements (REEs) and enrichment in heavy REEs, generally similar to normal mid-ocean ridge basalts (N-MORB). Specifically, Site C0012 samples display more pronounced positive anomalies in Rb, Ba, K, Pb and Sr, and negative anomalies in Th, U, Nb, and Ta, as well as negative Nb relative to La and Th. Site 1173 basalts have relatively uniform Sr-Nd-Pb isotopic compositions, close to the end member of depleted mantle, while Site C0012 samples show slightly enriched Sr-Nd-Pb isotopic signature, indicating a possible involvement of enriched mantle 1 (EM1) and EM2 sources, which could be attributed to the metasomatism of the fluids released from the dehydrated subduction slab, but with the little involvement of subducted slab-derived sedimentary component. Additionally, the Shikoku Basin record the formation of the back-arc basin was a mantle conversion process from an island arc to a typical MORB. The formation of the Shikoku Basin is different from that of the adjacent Japan Sea and Parece Vela Basin, mainly in terms of the metasomatized subduction-related components, the nature of mantle source, and partial melting processes. [ABSTRACT FROM AUTHOR]

Mass alkaline magmatic activities in Western Shandong during the late Mesozoic controlled the mineralization processes of gold and rare earth element (REE) polymetallic deposits in the region. The Chishan alkaline complex is closely associated with the mineralization of the Chishan REE deposit, which, as the third largest light REE deposit in China following the Baiyenebo (Inner Mongolia) and Mianning (Sichuan) deposits, is considered a typical example of alkaline rock mineralization throughout the North China Craton. To determine how the Chishan alkaline complex and REE deposit interact with each other, a systematic study was conducted on the petrology, rock geochemistry, zircon U–Pb geochronology, Lu–Hf isotopes of the quartz syenite, and alkali granite contained in the Chishan alkaline complex. The results reveal that the deposits feature similar geochemical characteristics typical of an alkaline rock series—both are rich in alkali, high in potassium, metaluminous, and poor in Ti, Fe, Mg, and Mn. In terms of REEs, the deposits are strongly rich in light REEs but poor in heavy REEs, with weak negative Eu anomalies. In terms of trace elements, they are rich in large ion lithophile elements Ba, Sr, and Rb but poor in high field-strength elements Nb, Ta, and Hf. Zircon LA-ICP-MS U–Pb dating indicated that the quartz syenite and alkali granite formed in Early Cretaceous at 125.8 ± 1.2 Ma and 127.3 ± 1.0 Ma, respectively; their εHf(t) values are −22.67 to −13.19, with depleted model ages (TDM) ranging from 1296 Ma to 1675 Ma and crustal model ages (TDMC) of 2036–2617 Ma. The Chishan alkaline complex originated from partial of the EM I-type (enriched mantle I) lithospheric mantle with assimilation of ancient crustal materials. The complex is of the same origin as the REE deposit, and developed in an extensional setting that resulted from plate subduction and lithospheric thinning and upwelling in the eastern area of the North China Craton. [ABSTRACT FROM AUTHOR]

The Akechukesai IV mafic–ultramafic complex, located in the western segment of the eastern Kunlun orogenic belt (EKOB), represents a newly-discovered complex, containing Ni ores at grades of up to 0.98% Ni. It is dominated by olivine pyroxenite, pyroxenite, and gabbro units. The gabbros are enriched in lithophile elements (e.g., Rb, U, and K) and light rare-earth elements (LREE), with negative anomalies in high field-strength elements, except Zr, Ta. Nb/Ta(∼5) and Zr/Hf (∼10) ratios lower than the primitive mantle and chondrites, respectively, indicate the influence of the mantle metasomatic process or fractionation of accessory mineral phases. Zircon U–Pb dating of the gabbro yielded an age of 423.9 ± 2.6 Ma, indicating that the complex formed contemporaneously with the Xiarihamu Ni deposit (423 ± 1 Ma). The gabbro has negative εHf(t) values (−11.3 to −1.2) with corresponding TDM1 ages of 1535–1092 Ma. The vein-like and disseminated mineralization (i.e., pyrite and pyrrhotite) have δ34S values of 13.1‰–13.4‰ and 5.0‰–8.5‰, respectively, suggesting that the magmas that formed the complex assimilated crustal sulfur. They yield 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb values of 17.323–18.472, 15.422–15.626, and 37.610–38.327, respectively, indicating Pb derived from multiple sources (i.e., mantle crustal sources). Geochemical and Hf–S–Pb isotopic characteristics suggest that the complex formed from a primitive magma derived by partial melting of a spinel- and garnet-bearing lherzolite mantle at variable degree of 5%–10%. This source region was geochemically enriched by previous interaction with slab-related fluids. Tectonic reconstruction suggests that the Akechukesai IV complex was generated in a post-collisional extensional environment. [ABSTRACT FROM AUTHOR]

The Xi'ao Cu-Sn polymetallic deposit is located in the inner alteration zone of the Laoka granite. The ore bodies extend to 400 m in the granite rock and primarily occur with fluorite and potassic alterations. Two cassiterite samples of altered rock-type ore and one tourmaline vein-type ore in the Xi'ao Cu-Sn polymetallic deposit yielded U-Pb ages of 83.3 ± 2.1 Ma, 84.9 ± 1.7 Ma, and 84.0 ± 5.6 Ma, respectively. The Raman spectrum peak values of A1g were shifted to a lower frequency, possibly due to the substitution of Sn with Nb, Ta, Fe, and Mn. Measured δ18O values of cassiterite samples and calculated δ18OH2O values for the ore-forming fluid indicate that the latter was mostly derived from magma. The high Fe and Mn abundances for cassiterite are consistent with those of hydrothermal origin. The Nb, Ta, and Ti contents indicate that cassiterites in the Xi'ao deposit likely formed in a metallogenic environment that was largely affected by granitic magmatism. Therefore, we conclude that the Xi'ao deposit is a magmatic hydrothermal deposit. [ABSTRACT FROM AUTHOR]

The nature and origin of the early Yanshanian granitoids, widespread in the South China Block, shed light on their geodynamic setting; however, understanding their magmatism processes remains a challenge. In this paper, we present both major and trace elements of bulk rock, Sr–Nd–Pb isotopic geochemistry, and zircon U–Pb–Hf isotopes of the low Sr and high Yb A2-type granites, which were investigated with the aim to further constrain their petrogenesis and tectonic implications. Zircon U–Pb dating indicates that these granites were emplaced at ca. 153 Ma. The granites are characterized by high SiO2 (>74 wt.%) and low Al2O3 content (11.0 wt.%–12.7 wt.%; <13.9 wt.%). They are enriched in large ion lithophile elements (LILEs) (e.g., Rb, Th, U, and K) and Yb, but depleted in high field-strength elements (HFSEs) (e.g., Nb, Ta, Zr and Hf), Sr, Ba P, Ti and Eu concentrations. They exhibit enriched rare earth elements (REEs) with pronounced negative Eu anomalies. They have εNd(t) values in a range from −6.5 to −9.3, and a corresponding TDM model age of 1.5 to 1.7 Ga. They have a (206Pb/204Pb)t value ranging from 18.523 to 18.654, a (207Pb/204Pb)t value varying from 15.762 to 15.797, and a (208Pb/204Pb)t value ranging from 39.101 to 39.272. The yield εHf(t) ranges from −6.1 to −2.1, with crustal model ages (TDMC) of 1.3 to 1.6 Ga. These features indicate that the low Sr and high Yb weakly peraluminous A2-type granites were generated by overlying partial melting caused by the upwelling of the asthenosphere in an extensional tectonic setting. The rollback of the Paleo-Pacific Plate is the most plausible combined mechanism for the petrogenesis of A2-type granites, which contributed to the Sn–W polymetallic mineralization along the Shi-Hang zone in South China. [ABSTRACT FROM AUTHOR]

Raman spectroscopy is a powerful tool used to identify mineral phases, study aqueous solutions and gas inclusions as well as providing crystallinity, crystallographic orientation and chemistry of mineral phases. When united with isotopic tracers, the information gained from Raman spectroscopy can be expanded and includes kinetic information on isotope substitution and replacement mechanisms. This review will examine the research to date that utilizes Raman spectroscopy and isotopic tracers. Beginning with the Raman effect and its use in mineralogy, the review will show how the kinetics of isotope exchange between an oxyanion and isotopically enriched water can be determined in situ. Moreover, we show how isotope tracers can help to unravel the mechanisms of mineral replacement that occur at the nanoscale and how they lead to the formation of pseudomorphs. Finally, the use of isotopic tracers as an in situ clock for mineral replacement processes will be discussed as well as where this area of research can potentially be applied in the future. [ABSTRACT FROM AUTHOR]