Trace elements in various genetic types of zircon from syenite of the Sakharjok massif,Kola Peninsula

Zircon is an accessory mineral in alkali and nepheline syenites of the Neoarchean Sakharjok intrusion. Zircon in association with britholite and pyrochlore forms orebodies in nepheline syenite of this massif. Zircon crystals reveal an inhomogeneous zonal, occasionally mosaic structure comprising fragments and zones related to magmatic, hydrothermal, and metamorphic stages of mineral formation. Magmatic zircon differs by a high REE concentration (1769 ppm, on average), distinct Ce maximum (Ce/Ce* = 105, on average), and Eu minimum (Eu/Eu* = 0.19) as compared with other genetic types. No correlation between these parameters has been established. Hydrothermal zircon is characterized by a low Ce/Ce* ratio (0.7–3.9 and 2.0, on average), elevated LREE contents, and lowered ratios of MREE and HREE to La. Metamorphic zircon differs from magmatic by a sharply lower REE concentration (385 ppm, on average), lowered Th/U (0.32) and Ce/Ce* (31.9, on average) ratios. In the Ce/Ce* versus MREE/La plot, the lowest values of these ratios are typical of hydrothermal zircon, while the intermediate and maximum values are inherent to metamorphic and magmatic zircons, respectively. These variations make it possible to delineate reliable fields of their compositions. The distribution of data points in the above-mentioned plots shows that REE chemical activity depends on the redox conditions of zircon crystallization.     

Magmatic-to-hydrothermal crystallization in the W–Sn mineralized Mole Granite (NSW, Australia): Part II: Evolving zircon and thorite trace element chemistry

The Sn–W mineralized Mole Granite in Eastern Australia hosts zircon populations that crystallized at several stages during a protracted magmatic to hydrothermal evolution. Thirty-four elements have been quantified by laser-ablation inductively-coupled-plasma mass-spectrometric microanalysis with the aim of relating the chemistry of zircon to its growth environment. Trace element contents are highly variable for all textural occurrences. Zircon inclusions in earliest quartz phenocryst suggest that zircon was a liquidus phase that crystallized probably deep in the crust. Trace element contents are conspicuously high, showing only a slight positive Ce anomaly but a pronounced negative Eu-anomaly. Successive crystallization stages of magmatic zircon are characterized by progressive depletion in trace element contents, notably the rare earth elements, with an increasingly important positive Ce-anomaly. This evolution reflects saturation of REE accepting minerals such as monazite, thorite, xenotime and possibly apatite and is affected little by the exsolution of a magmatic–hydrothermal fluid. Zircon that is interpreted to have precipitated from aqueous fluids in Sn–W-bearing quartz veins shows REE patterns indistinguishable from those of late magmatic zircon. When combined with experimental evidence on the fluid–melt partitioning of REE, it indicates that the REE distribution coefficients for zircon/melt and zircon/fluid are largely comparable.

The second example of hydrothermal zircon crystallized some 2 My after the host granite. These crystals reveal an intragranular zonation of increasing trace element concentrations from core to rim. Therefore, REE abundances and patterns alone are not conclusive indicators of the geological environment in which zircon crystallized. Nevertheless, variations in trace element contents of zircon that relate to the chemistry of the melt or fluid from which zircon crystallized, as measured in cogenetic melt and fluid inclusions, are promising for future petrogenetic modeling.

Lead and Cs are strongly incompatible in hydrothermal zircon, with estimated zircon–fluid distribution coefficients D ≤ 0.001, while Sn and Li are moderately incompatible, D_Sn  0.6 and D_Li  0.1, and Ce is compatible, D_Ce  14. Moreover, hydrothermal zircon has a more pronounced negative Eu-anomaly and higher Ta/Nb and U/Th ratios than the magmatic zircons of the Mole Granite.     

Mineral chemistry and Ti in zircon thermometry: Insights into magmatic evolution of the Sangan igneous rocks,NE Iran

The Sangan Magmatic complex (SMC) is, a large I-type magmatic complex, located in the northeastern Iran. Zircons extracted from the intrusive and volcanic rocks within the SMC record a similar Hf compositions and REE patterns, indicating that these chemical signatures have likely been inherited from the same source and simple history of magmatic crystallization during the evolution of the orogeny. The zircon from volcanic rocks yield Ti-in-zircon crystallization temperatures of 667–1145?°C with average temperatures of 934?°C while those from granitoids indicate crystallization temperatures of 614–898?°C with an average of 812?°C. Ti-in-zircon, Ti in biotite thermometries also indicates that the crystallization temperatures of volcanic rocks are relatively higher than those of granitoids. The biotite chemistry studies reveal that this mineral crystallized at approximately 725°–800?°C and 758° to 816?°C for granitoid and volcanic rocks, respectively, which is similar to obtained temperatures by Zir-saturation of Eq. (1). T_zicsat and T_magma trend lines on the T-SiO₂ diagram cross at high silica contents of ～68?wt.%, at which temperature the magma becomes zircon-saturated and new zircons are crystallized. The zircon REE data including Ce/Ce*, Eu/Eu*, and Th/U ratios suggest that SMC igneous rocks are formed from oxidized magma. However, the zircon Th/U and Hf data suggest that the SMC became progressively more oxidized and also indicate lower temperatures from volcanic and plutonic rock with decreasing time.     

Ti in zircon from the Boggy Plain zoned pluton: implications for zircon petrology and Hadean tectonics

The understanding of zircon crystallization, and of the Ti-in-zircon thermometer, has been enhanced by Ti concentration measurements of zircon from a small, concentrically zoned pluton in south-eastern Australia, the Boggy Plain zoned pluton (BPZP). Zircon crystals from rocks ranging in composition from gabbro to aplite were analysed for U–Th–Pb dating and Ti concentrations by an ion microprobe. Geochronological data yield a ²⁰⁶Pb/²³⁸U age of 417.2 ± 2.0 Ma (95% confidence) and demonstrate the presence of older inherited or xenocrystic zircon. Titanium measurements (n = 158) yield a mean Ti concentration of 11.7 ± 6.1 ppm (2SD) which corresponds to a mean crystallization temperature of 790°C for an α-TiO₂ = 0.74 (estimated using mineral equilibria), or 760°C for an α-TiO₂ = 1.0. Apparent zircon crystallization temperatures are similar in all intrusive phases, although the gabbro yields slightly higher values, indicating that crystallization occurred at the same temperature in all rock types. This finding is consistent with previous work on the BPZP, which indicates that liquid–crystal sorting (crystal fractionation) was the dominant control on chemical differentiation, and that late, differentiated liquids were similar in composition for all rock types. A simple forward model approximately predicts the range of crystallization temperatures, but not the shape of the distributions, due to sampling biases and complexities in the cooling and crystallization history of the pluton. The distribution of Ti concentrations has a mode at a higher Ti (higher temperature) than the sample set of Hadean detrital zircon. This is consistent with the hypothesis that the skew to low-T in the Hadean dataset is due to the presence of zircon that crystallized from wet anatectic melts.     

Geochemistry of magmatic and hydrothermal zircon from the highly evolved Baerzhe alkaline granite: implications for Zr–REE–Nb mineralization

The Baerzhe alkaline granite pluton hosts one of the largest rare metal (Zr, rare earth elements, and Nb) deposits in Asia. It contains a geological resource of about 100 Mt at 1.84 % ZrO₂, 0.30 % Ce₂O₃, and 0.26 % Nb₂O₅. Zirconium, rare earth elements (REE), and Nb are primarily hosted by zircon, yttroceberysite, fergusonite, ferrocolumbite, and pyrochlore. Three types of zircon can be identified in the deposit: magmatic, metamict, and hydrothermal. Primary magmatic zircon grains occur in the barren hypersolvus granite and are commonly prismatic, with oscillatory zones and abundant melt and mineral inclusions. The occurrence of aegirine and fluorite in the recrystallized melt inclusions hosted in the magmatic zircon indicates that the parental magma of the Baerzhe pluton is alkali- and F-rich. Metamict zircon grains occur in the mineralized subsolvus granite and are commonly prismatic and murky with cracks, pores, and mineral inclusions. They commonly show dissolution textures, indicating a magmatic origin with later metamictization due to deuteric hydrothermal alteration. Hydrothermal zircon grains occur in mineralized subsolvus granite and are dipyramidal with quartz inclusions, with murky CL images. They have 608 to 2,502 ppm light REE and 787 to 2,521 ppm Nb, much higher than magmatic zircon. The texture and composition of the three types of zircon indicate that they experienced remobilization and recrystallization during the transition from a magmatic to a hydrothermal system. Large amounts of Zr, REE, and Nb were enriched and precipitated during the transitional period to form the giant low-grade Baerzhe Zr–REE–Nb deposit.     

河西走廊晚泥盆世地层中冥古宙碎屑锆石的发现

河西走廊地区晚泥盆统中宁组地层中,利用LA-ICP-MS法测年获得了3.9Ga和4.0Ga两颗碎屑锆石,其Th/U依次为1.01和0.58,均为岩浆锆石。两颗锆石稀土元素呈轻稀土(LREE)亏损、重稀土(HREE)富集,均具有Ce正异常,其中4.0Ga锆石具有Eu负异常,3.9Ga锆石无Eu负异常。利用锆石中⁴⁹Ti的含量计算原岩岩浆温度分别为792±36℃(3.9Ga)和967±45℃(4.0Ga)。3.9Ga锆石获得原位Hf同位素结果,¹⁷⁶Hf/¹⁷⁷Hf_i=0.280169,ε_Hf(t)=-3.6,t_DM=4139Ma, t_DM^C=4319Ma。这两颗>3.9Ga碎屑锆石为西北地区首次发现,其微量元素特征说明在冥古宙时地球上可能存在地壳;结合前人古生物和古地磁研究结果,说明河西走廊在晚泥盆世时同澳大利亚西北部可能具有亲缘性。     

Magmatic and hydrothermal zircon growth during multiple orogenic cycles in an evolving mantle wedge

The Hongseong area of the Hongseong-Imjingang Belt in the central-western Korean Peninsula forms part of a subduction-collision system that is correlated with the Qinling-Dabie-Sulu Belt in China. Several serpentinized ultramafic bodies carrying blocks of metamorphosed mafic rocks occur in this area. Here we investigate zircon grains in serpentinites from Bibong(BB) and Wonnojeon(WNJ), and high-pressure(HP) mafic granulite from Baekdong(BD) localities based on U-Pb, REE and Lu-Hf analyses. The zircons from BD HP mafic granulite show distinct age peaks at 838 Ma, 617 Ma and 410 Ma, with minor peaks at1867 Ma, 1326 Ma and 167 Ma. The Neoproterozoic age peaks in these rocks as well as in the serpentinites suggest subduction-related melt-fluid interaction in the mantle wedge at this time. The older zircon grains ranging in age from the Early to Middle Paleoproterozoic might represent detrital grains from the basement rocks transferred to the wedge mantle through sediment subduction. The BD HP mafic granulite shows a Middle Paleozoic age peak(Devonian; 410 Ma). The 242-245 Ma age peaks in the compiled age data of zircon grains serpentinites from BB and WNJ correspond to a major Triassic event that further added melts and fluids into the ancient mantle wedge to crystallize new zircons. In the chondrite normalized rare earth element diagram, the magmatic zircon grains from the studied rocks show LREE depletion and HREE enrichment with sharply negative Eu and Pr anomalies and positive Ce and Sm anomalies. The REE patterns of hydrothermal zircons show LREE enrichment, and relatively flat patterns with negative Eu anomaly. Zircon Hf signature from the WNJ serpentinite show negative εHf(t)(-18.5 and-23.5) values indicating an enriched mantle source with TDM in the range of 1614 Ma and1862 Ma. Zircons from the BD HP mafic granulite also show slightly negative εHf(t)(average-4.3) and TDM in the range of 1365-1935 Ma. Our study provides evidence for multiple zircon growth in an evolving mantle wedge that witnessed melt and fluid interaction during different orogenic cycles.     

Host rock compositional controls on zircon trace element signatures in metabasites from the Austroalpine basement

Zircon populations of Neoproterozoic and early Paleozoic age occur in metabasites of a high-pressure amphibolite-facies unit of the Austroalpine basement south of the Tauern Window. The host rocks for these zircons are eclogitic amphibolites of N-MORB-type character, hornblende gneisses with volcanic-arc basalt signature, and alkaline within-plate-basalt amphibolites. Bulk rock magmatic trace element patterns were preserved during amphibolite-facies high-pressure and subsequent high-temperature events, as well as a greenschist-facies overprint. Positive Ce and negative Eu anomalies and enrichment of HREE in normalized zircon REE patterns, as analysed by LA-ICP-MS, are typical for an igneous origin of these zircon suites. Zircon Y is well correlated to HREE, Ce, Th, U, Nb, and Ta and allows discrimination of compositional fields for each host rock type. Low Th/U ratios are correlated to low Y and HREE abundances in zircon from low bulk Th/U host rocks. This is likely a primary igneous characteristic that cannot be attributed to metamorphic recrystallization. Variations of zircon/host rock element ratios confirm that ionic radii and charges control abundances of many trace elements in zircon. The trace element ratios—presented as mineral/melt distribution coefficients—indicate a selectively inhibited substitution of Zr and Si by HREE and Y in zircon which crystallized from a N-MORB melt. Correlated host rock and zircon trace element concentrations indicate that the metabasite zircons are not xenocrysts but crystallized from mafic melts, represented by the actual host rocks.     

General relations in the trace-element composition of zircons from eclogites with implications for the age of eclogites in the belomorian mobile belt

Analysis of currently available data (877 individual high-precision zircon analyses) on the composition of zircons from eclogite complexes worldwide reveals general relations in the zircon composition: an anomalous decrease in the Th concentration (no higher than 3 ppm on average) and the Th/U ratio (0.33 on average), a significant decrease in the concentrations of all REE (to 22 ppm) and particularly LREE (<2 ppm), and relatively low concentrations of Y (34 ppm), U (100 ppm), and P (41 ppm) at an elevated Hf concentration (11 400 ppm on average). The REE patterns of eclogitic zircons are noted for pronounced flat HREE patterns, poorly pronounced (if any) negative Eu anomalies, strongly reduced positive Ce anomalies (Ce/Ce* = 11 on average), and U-shaped configurations of LREE patterns up to the development of negative Nd anomalies. The relations detected in the distribution of trace elements and REE in eclogitic zircons are of universal nature and occur irrespective of the rock type (metabasites, metaultrabasites, or gneisses) and the metamorphic pressure (eclogites of high and ultrahigh pressure). The application of the aforementioned criteria makes it possible to reliable distinguish eclogitic zircons from those of magmatic or metamorphic genesis (not related to high-pressure metamorphism). Eclogites in the Belomorian Mobile Belt (in the Salma and Gridino areas) were determined to contain zircons in metagabbro eclogites; the cores of these zircons have an age of 2.8?C2.9 Ga and are of magmatic genesis, whereas their outer metamorphic zones have an age of 1.9 Ga and a trace-element composition typical of eclogitic zircons. Hence, the Belomorian Mobile Belt was affected only by single (Svecofennian, at ??1.9 Ga) episode of eclogite metamorphism of Archean rocks.     

Geochemistry and U–Pb age of zircons from the Vurechuaivench massif,Monchegorsk complex,Kola region

The paper presents data on the geochemical and geochronological characteristics of zircons from mafic rocks of part of the Monchegorsk layered complex represented by the Vurechuaivench massif. Ages of zircons (SHRIMP-II) from samples V-l-09 (anorthosite) and V-2-09 (gabbronorite) are dated back to 2508 ± 7 and 2504 ± 8 Ma, respectively. The chondrite-normalized REE patterns confirm the magmatic nature of zircons. The data unequivocally indicate that the U–Pb age of zircon from both gabbronorite and anorthosite corresponds to the age of melt crystallization in a magmatic chamber. The mantle origin of gabbroic rocks of the Vurechuaivench massif is confirmed by the REE patterns of three zircon generations with different crystallization sequences. The wide range of the Ce/Ce* ratio (9.96–105.24) established for zircons from gabbroic rocks of the Vurechuaivench massif indicates sharply oxidative conditions of zircon crystallization. For deepseated mantle rocks, these data can only be explained by significant contamination of the melt with country rock material.     

Formation Process of Zircon Associated with REE‐Fluorocarbonate and Niobium Minerals in the Nechalacho REE Deposit,Thor Lake,Canada

The two drill holes, which penetrated sub‐horizontal rare earth element (REE) ore units at the Nechalacho REE in the Proterozoic Thor Lake syenite, Canada, were studied in order to clarify the enrichment mechanism of the high‐field‐strength elements (HFSE: Zr, Nb and REE). The REE ore units occur in the albitized and potassic altered miaskitic syenite. Zircon is the most common REE mineral in the REE ore units, and is divided into five types as follows: Type‐1 zircon occurs as discrete grains in phlogopite, and has a chemical character similar to igneous zircon. Type‐2 zircon consists of a porous HREE‐rich core and LREE–Nb–F‐rich rim. Enrichment of F in the rim of type‐2 zircon suggests that F was related to the enrichment of HFSE. The core of type‐2 zircon is regarded to be magmatic and the rim to be hydrothermal in origin. Type‐3 zircon is characterized by euhedral to anhedral crystals, which occur in a complex intergrowth with REE fluorocarbonates. Type‐3 zircon has high REE, Nb and F contents. Type‐4 zircon consists of porous‐core and ‐rim, but their chemical compositions are similar to each other. This zircon is a subhedral crystal rimmed by fergusonite. Type‐5 zircon is characterized by smaller, porous and subhedral to anhedral crystals. The interstices between small zircon grains are filled by fergusonite. Type‐4 and type‐5 zircon grains have low REE, Nb and F contents. Type‐1 zircon is only included in one unit, which is less hydrothermally altered and mineralized. Type‐2 and type‐3 zircon grains mainly occur in the shallow units, while those of type‐4 and type‐5 are found in the deep units. The deep units have high HFSE contents and strongly altered mineral textures (type‐4 and type‐5) compared to the shallow units. Occurrences of these five types of zircon are different according to the depth and degree of the hydrothermal alteration by solutions rich in F and CO₃, which permit a model for the evolution of the zircon crystallization in the Nechalacho REE deposit as follows: (i) type‐1 (discrete magmatic zircon) is formed in miaskitic syenite. (ii) LREE–Nb–F‐rich hydrothermal zircon formed around HREE‐rich magmatic zircon (type‐2). (iii) type‐3 zircon crystallized through the F and CO₃‐rich hydrothermal alteration of type‐2 zircon which formed the complex intergrowth with REE fluorocarbonates; (iv) the CO₃‐rich hydrothermal fluid corroded type‐3, forming REE–Nb‐poor zircon (type‐4). Niobium and REE were no longer stable in the zircon structure and crystallized as fergusonite around the REE–Nb‐leached zircon (type‐4); (v) type‐5 zircon is formed by the more CO₃‐rich hydrothermal alteration of type‐4 zircon, suggested by the fact that type‐4 and type‐5 zircon grains are often included in ankerite. Type‐3 to type‐5 zircon grains at the Nechalacho REE deposit were continuously formed by leaching and/or dissolution of type‐2 zircon in the presence of F‐ and/or CO₃‐rich hydrothermal fluid. These mineral associations indicate that three representative hydrothermal stages were present and related to HFSE enrichment in the Nechalacho REE deposit: (i) F‐rich hydrothermal stage caused the crystallization of REE–Nb‐rich zircon (type‐2 rim and type‐3), with abundant formation of phlogopite and fluorite; (ii) F‐ and CO₃‐rich hydrothermal stage led to the replacement of a part of REE–Nb–F‐rich zircon by REE fluorocarbonate; and (iii) CO₃‐rich hydrothermal stage resulted in crystallization of the REE–Nb–F‐poor zircon and fergusonite, with ankerite. REE and Nb in hydrothermal fluid at the Nechalacho REE deposit were finally concentrated into fergusonite by way of REE–Nb–F‐rich zircon in the hydrothermally altered units.     

Rare earth element and stable isotope (O, S) geochemistry of barite from the Bijgan deposit, Markazi Province, Iran

The Bijgan barite deposit, which is located northeast of Delijan in Markazi Province of Iran, occurs as a small lenticular body at the uppermost part of an Eocene volcano-sedimentary rock unit. The presence of fossiliferous and carbonaceous strata suggests that the host rocks were deposited in a quiet marine sedimentary environment. Barite, calcite, iron oxides and carbonaceous clay materials are found as massive patches as well as thin layers in the deposit. Barite is marked by very low concentrations of Sr (1–2%) and total amounts of rare earth elements (REEs) (6.25–17.39?ppm). Chondrite-normalized REE patterns of barite indicate a fractionation of light REEs (LREEs) from La to Sm, similar to those for barite of different origins from elsewhere. The La_CN/Lu_CN ratios and chondrite-normalized REE patterns reveal that barite in the Bijgan deposit is enriched in LREE relative to heavy rare earth elements (HREEs). The similarity between the Ce/La ratios in the barite samples and those found in deep-sea barite supports a marine origin for barite. Lanthanum and Gd exhibit positive anomalies, which are common features of marine chemical sediments. Cerium shows a negative anomaly in most samples that was inherited from the negative Ce anomaly of hydrothermal fluid that mixed with seawater at the time of barite precipitation. The δ¹⁸O values of barites show a narrow range of 9.1–11.4‰, which is close to or slightly lower than that of contemporaneous seawater at the end of the Eocene. This suggests a contribution of oxygen from seawater in the barite-forming solution. The δ³⁴S values of barites (9.5–15.3‰) are lower than that of contemporaneous seawater, which suggests a contribution of magmatic sulfur to the ore-forming solution. The oxygen and sulfur isotope ratios indicate that submarine hydrothermal vent fluids are a good analog for solutions that precipitated barite, due to similarities in the isotopic composition of the sulfates. The available data including tectonic setting, host rock characteristics, REE geochemistry, and oxygen and sulfur isotopic compositions support a submarine hydrothermal origin for the Bijgan barite deposit. At the seafloor, barite deposition occurred where ascending Ba-bearing hydrothermal fluids encountered seawater. Sulfate was derived from the sulfate-bearing marine waters, and, to a lesser extent, by oxidized H₂S, which was derived from magmatic hydrothermal fluids.     

Origin of natural sulfur-metal chimney in the Tangyin hydrothermal field,Okinawa Trough: constraints from rare earth element and sulfur isotopic compositions

For the first time, we present the rare earth element (REE) and sulfur isotopic composition of hydrothermal precipitates recovered from the Tangyin hydrothermal field (THF), Okinawa Trough at a water depth of 1206 m. The natural sulfur samples exhibit the lowest ΣREE concentrations (ΣREE= 0.65×10^–6–4.580×10^–6) followed by metal sulfides (ΣREE=1.71×10^–6–11.63×10^–6). By contrast, the natural sulfur-sediment samples have maximum ΣREE concentrations (ΣREE=11.54×10^–6–33.06×10^–6), significantly lower than those of the volcanic and sediment samples. Nevertheless, the δEu, δCe, (La/Yb)_N, La/Sm, (Gd/Yb)_N and normalized patterns of the natural sulfur and metal sulfide show the most similarity to the sediment. Most hydrothermal precipitate samples are characterized by enrichments of LREE (LREE/HREE=10.09–24.53) and slightly negative Eu anomalies or no anomaly (δEu=0.48–0.99), which are different from the hydrothermal fluid from sediment-free mid-oceanic ridges and back-arc basins, but identical to the sulfides from the Jade hydrothermal field. The lower temperature and more oxidizing conditions produced by the mixing between seawater and hydrothermal fluids further attenuate the leaching ability of hydrothermal fluid, inducing lower REE concentrations for natural sulfur compared with metal sulfide; meanwhile, the negative Eu anomaly is also weakened or almost absent. The sulfur isotopic compositions of the natural sulfur (δ³⁴S=3.20‰–5.01‰, mean 4.23‰) and metal sulfide samples (δ³⁴S=0.82‰–0.89‰, mean 0.85‰) reveal that the sulfur of the chimney is sourced from magmatic degassing.     

Zircon U-Pb geochronology and geochemistry of Late Devonian–Carboniferous granitoids in NW Iran: implications for the opening of Paleo-Tethys

ABSTRACT

We present zircon U-Pb crystallization ages combined with bulk rock major and trace element geochemistry and Sr-Nd-Pb and zircon in-situ Hf isotopic compositions of the Amand and Moro granitoid intrusions in northwest Iran. The Amand and Moro plutons include granite and syeno-diorite with LA-ICP-MS U-Pb zircon ages of 367 ± 6.8 Ma and 351 ± 1.3 Ma, respectively, representative of Late Devonian-Early Carboniferous magmatic activity in NW Iran. Geochemical characteristics such as typical enrichments in alkalis, Nb, Zr, Ga and Y, depletion in P and Sr and fractionated REE patterns with high Ga/Al ratios and Eu negative anomalies are consistent with A-type magmatic signatures. The granitoids are classified as A₂-type and within-plate granitoids. The bulk rock geochemistry (enrichments in Th, Nb and, high Th/Yb, Zr/Y ratios) along with low variation of ¹⁴³Nd/¹⁴⁴Nd_(i) and ⁸⁷Sr/⁸⁶Sr_(i) ratios and positive zircon εHf_(t) support the role of a mantle plume component for the evolution of the Amand and Moro A-type granitoids in an extensional tectonic environment. In fitting with wider regional knowledge, this magmatism occurred during Paleo-Tethys opening in northern Gondwana.     

Neoarchean crust-mantle interactions in the Yishui Terrane,south-eastern margin of the North China Craton: Constraints from geochemistry and zircon U-Pb-Hf isotopes of metavolcanic rocks and high-K granitoids

The Neoarchean Yishui Terrane (YST) is situated in the east of Western Shandong Province (WSP), south-eastern margin of the North China Craton (NCC). The metavolcanic rocks of the YST are fine-grained hornblende plagioclase gneisses (Group #1) and fine-grained amphibolites (Group #2) in the Yangzhuangzhen area and fine- to medium-grained amphibolites (Group #3) in the Leigushan area. The high-K granitoids associated with Groups #1 and 2 are dominated by fine- to medium-grained monzogranitic gneisses. Zircon LA-ICP-MS U-Pb dating reveals that the magmatic precursors of Groups #1 and #2 were formed at 2641 Ma and the magmatic precursors of concomitant monzogranitic gneisses were emplaced from 2615 to 2575 Ma, whereas Group #3 represents a later 2500 Ma volcanic eruption, and all these metamorphic volcanic rocks and monzogranitic gneisses were subjected to subsequent 2470–2460 Ma metamorphism.The metamorphic volcanic rock samples in Group #1 exhibit the chemical compositions of calc-alkaline andesites, showing fractionated chondrite-normalized REE patterns ((La/Yb)_N = 10.48–19.30) and negative Nb, Ta and Ti anomalies ((Nb/La)_PM = 0.13–0.22), which are akin to those of typical high-Mg andesites (HMAs) in the subduction-related settings. The magmatic precursors of the Group #1 samples were derived from partial melting of a fluid- or melt-metasomatized depleted mantle wedge at deep levels in the upper mantle. Samples in Group #2 show calc-alkaline chemical compositions with less fractionated chondrite-normalized REE patterns ((La/Yb)_N = 2.24–3.34) and negative Nb, Ta and Ti anomalies ((Nb/La)_PM = 0.47–0.76), which are consistent with those of the volcanic rocks in the Aleutian island arc. The magmatic precursors of Group #2 were generated by partial melting of a fluid-metasomatized depleted mantle wedge at shallow levels in the upper mantle. The monzogranitic gneisses exhibit high SiO₂ and K₂O contents with high-K calc-alkaline affinities and peraluminous characteristics. Based on their distinct HREE contents and chondrite-normalized REE patterns, these granitoid samples are subdivided into low-Yb monzogranitic gneisses (LYMGs) and high-Yb monzogranitic gneisses (HYMGs). The LYMG magma was derived from partial melting of a mixed source of juvenile two-mica pelites and minor basic-intermediate igneous rocks at lower crustal levels with pyroxene + amphibole + garnet as the main residual phases, and the HYMG magma was derived from partial melting of multi-sourced juvenile two-mica pelites at middle to lower crustal levels with pyroxene + amphibole and subordinate plagioclase and garnet as the main residual phases. In addition, Group #3 resembles tholeiitic back-arc basalts in the Okinawa Trough and displays flat chondrite-normalized REE patterns ((La/Yb)_N = 1.22–2.08) and slightly negative Nb and Ta anomalies ((Nb/La)_PM = 0.35–0.59). This group was most likely derived from partial melting of a depleted mantle source that had been modified by the addition of subducted slab-derived fluids at shallow levels in the upper mantle. These metavolcanic rocks and concomitant high-K granitoids record important Neoarchean crust-mantle interactions involving the first modification and partial melting of the lithospheric mantle induced by oceanic crust subduction; then, upwelling and underplating of mantle-derived magmas triggered partial melting of the middle to lower crust and mixing between crust- and mantle-derived magmas. These processes imply that Neoarchean crust-mantle interaction played a crucial role in the evolution of the southeastern margin of the NCC.Available whole-rock Sm-Nd and zircon Lu-Hf isotopic data from metamorphic volcanic rocks and plutonic granitoids from this study and previous studies reveal that YST experienced three crucial juvenile crustal growth events from ~2.78–2.69 Ga, ~2.64–2.56 Ga and ~2.54–2.50 Ga.     

Ion-microprobe zircon geochemistry as an indicator of mineral genesis during geochronological studies

This paper considers the distribution of trace elements (including rare earth elements) in zircons dated by the ion-microprobe U-Th-Pb isotope method and its genetic implications. Two problems were addressed on the basis of the investigation of trace element compositions of zircons: (1) genesis of zircons from subalkaline magmatic rocks, sysenites, and sanukitoids and their comparison with tonalites as exemplified by the rocks of the Karelian region, and (2) determination of trace element signatures of zircons from the oldest granulite-facies rocks of the Ukrainian shield. It was shown that the REE distribution patterns of the tonalites, which crystallized in equilibrium with melt, are strictly governed by crystal-chemical laws. The REE distribution patterns show a positive slope with an increase from La to Lu, a positive Ce anomaly, and a negative Eu anomaly. Similar patterns were observed in zircons from the syenites. The trace element contents of zircons are related to those of melts through partition coefficients. Zircons from the sanukitoids show a considerable LREE enrichment, which is inconsistent with the calculated zircon/melt partition coefficients and presumably related to the inherently imperfect zircon structure. Such a structure was formed during zircon crystallization from melt at high temperatures and the anomalous fluid regime that is characteristic, in particular, of sanukitoid melts. The REE distribution patterns of zircons that crystallized under granulite-facies conditions are sharply different from typical distributions in HREE depletion, which was caused by the competitive growth of garnet during zircon crystallization.     

1.74 Ga crustal melting after rifting at the northern Indian margin: investigation of mylonitic orthogneisses in the Kathmandu area,central Nepal

ABSTRACT

Mylonitic orthogneisses in the Kathmandu area, central Nepal have been investigated using whole-rock and mineral chemistry, Rb-Sr isotopes, and zircon U-Pb age dating. Zircon REE patterns determined from orthogneisses are characterized by enriched HREE patterns and the prominent Eu anomalies, consistent with a magmatic origin. The U-Pb zircon age dating and Ti-in-zircon thermometry revealed crystallization took place ca. 1.74 Ga at temperatures of 705–765℃; typical of felsic magmatism in the crust. Whole-rock data from most orthogneisses in this study and from similar rocks in previous studies span the ‘syn-collisional’ and ‘post-collisional’ fields on various tectonic discrimination diagrams, while some data also plot in rift-related magmatism fields. The peraluminous compositions, very high Sr isotopic ratios (0.865–3.585) and high Th and U concentrations for all orthogneisses in this study indicate that mylonitic orthogneisses are largely of S-type crustal origins. The new data presented herein, combined with that of previous studies, outline at least two Palaeoproterozoic magmatic episodes: 1) ca. 1.92–1.90 Ga rift-related magmatism derived from mantle melting and 2) 1.84–1.74 Ga crustal melting, resulting from burial of the Indian basement during thermal subsidence after rifting. This two-stage Palaeoproterozoic magmatism in Nepal occurred along the northern passive margin of the Indian basement during and/or after the breakup of the Columbia supercontinent.     

LA-ICP-MS U-Pb zircon dating of the Bozhushan granite in Southeast Yunnan

The LA-ICP-MS U-Pb zircon dating of eight typical samples from four units of the Bozhushan granite intrusion in southeastern Yunnan Province, constrains the age of acidic magmatic intrusion in this area. Both the oscillatory zoning and chondrite-normalized REE patterns characterized by LREE-depletion and HREE-enrichment with positive Ce anomaly and negative Eu anomaly indicate the magmatic genesis of these zircons. Eight zircon samples from the Bozhushan granite yielded a mean 206 Pb/ 238 U age of (85.58±1.0) Ma (MSWD=4.1) to (88.10±0.66) Ma (MSWD=1.8). These chronology data suggest an accurate isotopic age for the intrusion of the Bozhushan granite, and are different from the published age data of 48 to 111.5 Ma. The geochronology data of the Gejiu, Dulong and Dachang super-large deposits and related Yanshanian granites indicated that there occurred large-scale granitic magmatism and mineralization events in western Nanling region during the Late Cretaceous.     

华北地台北缘鞍山白家坟奥长花岗岩地球化学特征、锆石U-Pb年龄及意义

太古宙TTG岩石的成因及年代学研究是理解前板块构造和板块构造开始及其演化过程的关键,是陆壳增生的重要标志,为太古宙地质体研究的热点和难点之一。对鞍山地区的白家坟岩体进行了地球化学研究和锆石U-Pb测年。数据结果显示,该岩体具有正片麻岩特征,Si、Na含量高,TFeO、MgO、CaO含量低,轻、重稀土元素分异程度低,且具有一定变化。稀土元素总量偏低(12.6×10~(-6)～119.34×10~(-6)),LREE/HREE值为8.98～13.11。微量元素富集K、Rb、Ba,亏损Nb、Ce、Zr、Sm、Ti、Y、Yb;K/Rb平均值为229.37,Rb/Sr平均值为0.58,Ba/Sr平均值为3.28,Y/Nb平均值为3.36。表明该岩体为岩浆作用的产物,也有部分为壳内再循环的产物或受到陆壳物质影响。测得~(207)Pb/~(206)Pb年龄加权平均值为3816±14Ma,锆石具有清晰的振荡环带结构,所有核部锆石分析点的Th/U值在0.05～0.54之间,具有岩浆锆石的特点,代表了白家坟奥长花岗质岩石的结晶时代。3613～3651Ma和3331Ma两组年龄数据代表早太古代的一次岩浆事件及重要的陆壳增生时期的热事件。