The origin of variable-δ18O zircons in Jurassic and Cretaceous Mo-bearing granitoids in the eastern Xing–Meng Orogenic Belt,Northeast China

This study reports new zircon U–Pb ages, Lu–Hf isotope data, and oxygen isotope data for Mesozoic Mo-bearing granitoids in the eastern Xing–Meng Orogenic Belt (XMOB) of Northeast China, within the eastern Central Asian Orogenic Belt. Combining these new laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) zircon U–Pb ages with the results of previous research indicates that two stages of Mo-bearing granitoid magmatism occurred in the eastern XMOB, during the Early–Middle Jurassic (200–165 Ma) and the Early Cretaceous (ca. 111 Ma). The eastern XMOB also contains Mo-bearing granitoids with variable δ¹⁸O compositions that record variations in source oxygen isotopic compositions. Combining δ¹⁸O data with zircon U–Pb and Hf isotopic data provides evidence of the origin of these granitoids. Three types of zircon have been identified within these granitoids. Type 1 zircons formed during the Mesozoic and having high δ¹⁸O values (5.71–7.05‰) that are consistent with the compositions of magmatic zircons from the Luming, Jiapigou, and Kanchuangou areas. These zircons suggest that the Mo-bearing granitoids were derived from a source containing supracrustal materials. The type 2 zircons have extremely low and heterogeneous δ¹⁸O values (4.64–4.89‰) that are consistent with the compositions of magmatic zircons from the Jidetun and Fuanpu areas. These magmas were generated by the remelting of juvenile crustal material that was previously significantly modified by interaction with fluids. Type 3 zircons generally have mantle-like δ¹⁸O values (5.42–5.57‰), with several zircons yielding higher δ¹⁸O values, suggesting that these intrusions formed from mantle-derived magmas that assimilated and were metasomatized by crustal material. Combining these geochemical data with the geology of this region indicates that the Mo-bearing granitoids were generated as a result of subduction of the Palaeo-Pacific Plate beneath the Eurasian continent.     

Magmatic garnet in the Triassic (215 Ma) Dehnow pluton of NE Iran and its petrogenetic significance

The Triassic Dehnow pluton of NE Iran is a garnet-bearing I-type calc-alkaline metaluminous diorite-tonalite-granodiorite intrusion. The parental magma formed as the result of partial melting of intermediate to felsic rocks in the lower crust. Petrological and geochemical evidence, which indicates a magmatic origin for the garnet, includes: large size (~10–20 mm) of crystals, absence of reaction rims, a distinct composition from garnet in adjacent metapelitic rocks, and similarity in the composition of mineral inclusions (biotite, hornblende) in the garnet and in the matrix. Absence of garnet-bearing enclaves in the pluton and lack of sillimanite (fibrolite) and cordierite inclusions in magmatic garnet suggests that the garnet was not produced by assimilation of meta-sedimentary country rocks. Also, the δ¹⁸O values of garnet in the pluton (8.3–8.7‰) are significantly lower than δ¹⁸O values of garnet in the metapelitic rocks (12.5–13.1‰). Amphibole-plagioclase and garnet-biotite thermometers indicate crystallization temperatures of 708°C and 790°C, respectively. A temperature of 692°C obtained by quartz-garnet oxygen isotope thermometry points to a closure temperature for oxygen diffusion in garnet. The composition of epidote (X_ep) and garnet (X_adr) indicates ~800°C for the crystallization temperature of these minerals. Elevated andradite content in the rims of garnet suggests that oxygen fugacity increased during crystallization.     

Oxygen isotope composition of syngenetic inclusions in diamond from the Finsch Mine,RSA

Oxygen isotope data have been obtained for silicate inclusions in diamonds, and similar associated minerals in peridotitic and eclogitic xenoliths from the Finsch kimberlite by laser-fluorination. Oxygen isotope analyses of syngenetic inclusions weighing 20–400 μg have been obtained by laser heating in the presence of ClF₃. ¹⁸O/¹⁶O ratios are determined on oxygen converted to CO₂ over hot graphite and, for samples weighing less than 750 μg (producing <12 μmoles O₂) enhanced CO production in the graphite reactor causes a systematic shift in both δ¹³C and δ¹⁸O that varies as a function of sample weight. A “pressure effect” correction procedure, based on the magnitude of δ¹³C (CO₂) depletion relative to δ¹³C (graphite), is used to obtain corrected δ¹⁸O values for inclusions with an accuracy estimated to be ±0.3‰ for samples weighing 40 μg.Syngenetic inclusions in host diamonds with similar δ¹³C values (−8.4‰ to −2.7‰) have oxygen isotope compositions that vary significantly, with a clear distinction between inclusions of peridotitic (+4.6‰ to +5.6‰) and eclogitic paragenesis (+5.7‰ to +8.0‰). The mean δ¹⁸O composition of olivine inclusions is indistinguishable from that of typical peridotitic mantle (5.25 ± 0.22‰) whereas syngenetic purple garnet inclusions possess relatively low δ¹⁸O values (5.00 ± 0.33‰). Reversed oxygen isotope fractionation between olivine and garnet in both diamond inclusions and diamondiferous peridotite xenoliths suggests that garnet preserves subtle isotopic disequilibrium related to genesis of Cr-rich garnet and/or exchange with the diamond-forming fluid. Garnet in eclogite xenoliths in kimberlite show a range of δ¹⁸O values from +2.3‰ to +7.3‰ but garnets in diamondiferous eclogites and as inclusions in diamond all have values >4.7‰.     

A Nd- and O-isotope study of the REE-rich peralkaline Strange Lake granite: implications for Mesoproterozoic A-type magmatism in the Core Zone (NE-Canada)

It is well established that A-type granites enriched in high field strength elements, such as Zr, Nb and the REE, form in anorogenic tectonic settings. The sources of these elements and the processes controlling their unusual enrichment, however, are still debated. They are addressed here using neodymium and oxygen isotope analyses of samples from the 1.24 Ga Strange Lake pluton in the Paleoproterozoic Core Zone of Québec-Labrador, an A-type granitic body characterized by hyper-enrichment in the REE, Zr, and Nb. Age-corrected εNd values for bulk rock samples and sodic amphiboles (mainly arfvedsonite) from the pluton range from ?0.6 to ?5.7, and ?0.3 to ?5.3, respectively. The εNd values for the Napeu Kainiut quartz monzonite, which hosts the pluton, range from ?4.8 to ?8.1. The ¹⁴⁷Sm/¹⁴⁴Nd ratios of the suite and the host quartz monzonite range from 0.0967 to 0.1659, large variations that can be explained by in situ fractionation of early LREE-minerals (Strange Lake), and late hydrothermal HREE remobilization. Oxygen isotope analyses of quartz of both Strange Lake and the host yielded δ¹⁸O values between +8.2 and +9.1, which are considerably higher than the mantle value of 5.7 ± 0.2‰. Bulk rock oxygen isotope analyses of biotite-gneisses in the vicinity of the Strange Lake pluton yielded δ¹⁸O values of 6.3, 8.6 and 9.6‰. The negative εNd values and positive δ¹⁸O values of the Strange Lake and Napeu Kainiut samples indicate that both magmas experienced considerable crustal contamination. The extent of this contamination was estimated, assuming that the contaminants were sedimentary-derived rocks from the underlying Archean Mistinibi (para-) gneiss complex, which is characterized by low εNd and high δ¹⁸O values. Mixing of 5–15% of a gneiss, having an εNd value of ?15 and a δ¹⁸O value of +11, with a moderately enriched mantle source (εNd = +0.9, δ¹⁸O = +6.3) would produce values similar to those obtained for the Strange Lake granites. Based on analogies between the Nain Plutonic Suite and the Gardar alkaline igneous province (SW-Greenland), we conclude that the Strange Lake pluton and associated REE-mineralized anorogenic bodies formed from a combination of subduction-induced fertilization of the sublithospheric mantle, crustal extension and in situ magma evolution.     

Local distribution of oxygen isotopes and fluid exchange during genesis of the corundum-bearing rocks of Khitostrov Island

New data are presented on the distribution of oxygen isotopes and conditions of the local isotope equilibrium in high-Al rocks rocks of Khitostrov Island showing abnormally low δ¹⁸O values (below–25‰). The temperatures of isotope equilibrium are within 400–475°C. The minimum δ¹⁸O values have been registered in the in plagioclase, whereas the same phases in kyanite-bearing rocks lacking corundum demonstrate δ¹⁸O values usually 3–5‰ higher. The fluid δ¹⁸O value varies from–22 to–16‰ at 475 ± 15°C, from–18 to–23‰ at 425 ± 25°C, and from–17 to–22‰ at 380 ± 15°C. The results obtained do not require abnormal depletion of δ¹⁸O values owing to the infiltration of an external fluid under the Svecofennian transformations. The association of corundum-bearing rocks with the basic intrusions, the presence of zircon cores of older ages compared to these rocks, and the peculiarities of rock chemistry may be ascribed to the fact that lower crustal layers of ancient rocks depleted in δ¹⁸O before metamorphism were captured by basite melts.     

Oxygen isotope signatures in olivines from São Miguel (Azores) basalts: implications for crustal and mantle processes

Oxygen isotope ratios were measured in olivines from eight São Miguel basalt lavas. With one exception (4.57‰), the olivines are indistinguishable from one another with an average δ¹⁸O of 4.92±0.03‰ (1σ). This value is slightly lower than that characteristic of upper mantle peridotite and MORB olivines (5.2±0.2‰). Assimilation of ≥10–20% of high-temperature altered lower oceanic crust or 4–9% hydrothermally altered volcanic edifice rocks could produce the low δ¹⁸O signatures in the São Miguel olivines; both of these assimilation models are permitted by the trace element and radiogenic isotope variations in the São Miguel basalts. However, the limited variation in δ¹⁸O despite eruption of the basalts through compositionally and tectonically variable lithosphere, and the lack of correlation of δ¹⁸O with olivine forsterite content, are more easily explained if the olivine δ¹⁸O signatures are inherited from their mantle source. If the δ¹⁸O signatures reflect mantle source compositions, then the relatively low and uniform δ¹⁸O signatures allow constraints to be placed on the origin of the mantle sources beneath São Miguel. Extreme variations in radiogenic isotope signatures have previously been attributed to two component source mixing between a predominant Azores plume source with mild HIMU-like characteristics, and an EMII-type mantle with very radiogenic Sr. The low δ¹⁸O signatures in the São Miguel basalt olivines suggest that the predominant Azores plume source contains >10% hydrothermally altered recycled oceanic crust. The limited variation in δ¹⁸O is consistent with a component of recycled sediment in the São Miguel EMII-type source, although, unlike the case for other EMII OIB (e.g. Samoa and Society), the relatively low δ¹⁸O signatures in São Miguel restrict any involvement of recycled sediment to <2% of a relatively low δ¹⁸O and very radiogenic Sr or high Rb/Sr sediment. Involvement of several percent metasomatized subcontinental lithospheric mantle could alternatively produce the EMII-type Sr–Nd–Pb isotope signatures without significantly affecting the plume-related low δ¹⁸O signatures. The São Miguel δ¹⁸O data are thus consistent with mixing between a low δ¹⁸O Azores plume source with a component of subducted, hydrothermally altered lower oceanic crust, and either minor recycled sediment or localized EMII-rich delaminated subcontinental lithospheric mantle. The latter could have been introduced into the lithosphere or shallow asthenosphere during opening of the Atlantic ocean basin.     

Ediacaran Águas Belas pluton,Northeastern Brazil: Evidence on age,emplacement and magma sources during Gondwana amalgamation

Ediacaran syenogranites from the Águas Belas pluton, Borborema Province, Northeastern Brazil were investigated in this work. The studied granitoids show high SiO₂, Fe# [FeO / (FeO + MgO)], total alkalis (K₂O + Na₂O) and BaO contents and medium Sr and low Nb contents. They show gentle fractionated rare earth patterns with discrete Eu negative anomalies. Major and trace element data point to chemical features of transitional high-K calc-alkaline to alkaline post-collisional magmatism. Structural data coupled with geochronological data suggest that NNE–SSW-trending sinistral movements at shear zones were initiated at ca. 590 Ma and have activated E–W pre-existing structures at the current crustal level. The synchronism of these shear zones allowed the dilation to generate the necessary space for the emplacement of the Águas Belas pluton.U–Pb SHRIMP zircon data show a cluster of ages around 588 ± 4 Ma which is interpreted as the crystallization age. Some zircon grain cores yielded ages within 2060–1860 Ma and 1670–1570 Ma intervals. Oxygen isotope compositions of zircon grains with distinct ages were measured using SHRIMP techniques. Twenty three analyses in the same zircon spots previously analyzed for U–Pb show δ¹⁸O values ranging from 5.79‰ to 10.30‰ SMOW. This large range of values results from variations both between grains and within grains (core–mantle/rim), and is interpreted as the result of mixing of components with distinct oxygen isotope compositions. The U–Pb zircon ages and the δ¹⁸O values associated with Paleoproterozoic Nd T_DM model ages suggest that the protolith of these granitoids involved a mantle component (Paleoproterozoic lithospheric mantle), Paleoproterozoic and Mesoproterozoic igneous rocks. Interactions with Mesoproterozoic or Neoproterozoic supracrustal rocks, may have occurred during the intrusion. The resulting magma evolved through biotite and K-feldspar fractionation.     

Sub-arc mantle heterogeneity in oxygen isotopes: evidence from Permian mafic–ultramafic intrusions in the Central Asian Orogenic Belt

Integrated zircon–olivine O–Hf isotope data have been successfully used to unravel the nature of the source mantle for the early Permian post-collisional mafic–ultramafic intrusive rocks in the southern margin of the Central Asian Orogenic Belt in NW China. Olivine crystals with forsterite (Fo) contents varying from 91 to 87 mol% from the Permian Pobei mafic–ultramafic complex in the region yield highly elevated δ¹⁸O from 6.0 to 7.2‰. These values are much higher than typical mantle values (~?5.3‰) and are apparently at odds with the mantle-like ε_Nd(t) values of whole rocks (4.9–5.4). Magmatic zircon crystals from troctolite and gabbroic rocks show divergent oxygen and hafnium isotopic compositions: mantle-like ε_Hf(t) values from 5.1 to 11.9 and crust-like δ¹⁸O values from 7.6 to 10.1‰. The observed increase of δ¹⁸O values from olivine (an early crystallizing phase) to zircon (a late crystallizing phase) in the mafic–ultramafic rocks is generally consistent with an AFC process. However, this process cannot fully explain the highly elevated δ¹⁸O values (6–7‰) for the most primitive olivine containing Fo as high as mantle olivine (>?90 mol%) and the mantle-like Hf isotope composition of zircon. Mixing calculation indicates that such highly unusual isotope compositions can be explained by the previous source mantle contamination with subducted sediment-derived melts and slab-derived fluids. Our results show that the combination of zircon O–Hf isotopes and olivine oxygen isotopes is more effective than the data of zircon or olivine alone to distinguish the effect of AFC process from source contamination. The results from this study provide a new line of evidence that the sub-arc mantle is not homogeneous in oxygen isotopes.     

Oxygen isotopic study of Late Mesozoic cooling of the Mount Barcroft area,central White Mountains,eastern California

The Middle Jurassic Barcroft mafic granodiorite and Late Cretaceous, ternary-minimum McAfee Creek Granite are important components of the igneous arc sited along the SW North American margin. Bulk-rock analyses of 11 samples of the metaluminous, I-type Barcroft comagmatic suite have an average δ¹⁸O value of 7.4±0.6‰ (all values±1σ). Four Barcroft specimens average ε_Nd=?3.6±1.8, ⁸⁷Sr/⁸⁶Sr=0.707±0.001. The pluton consists of petrochemically gradational, Ca-amphibole-rich gabbro/diorite, granodiorite, metadiorite, and rare alaskite–aplite; for most of the pluton, oxygen isotope exchange of quartz, feldspar(s), biotite, and Ca-amphibole accompanied local deuteric alteration. Eight specimens of slightly peraluminous granitic rocks of the muscovite-bearing McAfee Creek series have an average δ¹⁸O of 8.6±0.5‰. Four McAfee-type samples average ε_Nd=?7.8±1.7, ⁸⁷Sr/⁸⁶Sr=0.711±0.004. For both plutons, bulk-rock evidence of exchange with near-surface water is lacking, suggesting ~5–10 km cooling depths. Barcroft minerals exhibit regular oxygen isotopic partitioning from high to low δ¹⁸O in the sequence quartz>plagioclase>K-feldspar>>amphibole≥biotite. Along the SE margin of the pluton, quartz and biotite in Lower Cambrian quartzites are higher in δ¹⁸O, and show slightly larger fractionations than igneous analogues. Exchange with fluids derived from these heated, contact-metamorphosed country rocks increased bulk ¹⁸O/¹⁶O ratios of Barcroft border rocks (and constituent plagioclase+subsolidus tremolite–actinolite), especially of granitic dikes transecting the wall rocks. Oxygen isotope thermometry for seven Barcroft pluton quartz–amphibole and six quartz–biotite pairs indicate apparent subsolidus temperatures averaging 519±49 °C. Quartz–plagioclase pairs from two Barcroft granodiorites yield values of 519 and 515 °C. A quartz–biotite pair from a quartzite adjacent to the Barcroft pluton yields an apparent temperature of 511 °C, in agreement with estimates based on contact metamorphic parageneses. Except for its SE margin, Barcroft pluton silicates evidently exchanged oxygen isotopes under local deuteric conditions. Compatible with Ca-amphibole thermobarometric analyses, areal distributions for quartz–plagioclase, quartz–amphibole, and quartz–biotite pairs reveal that putative annealing temperatures are lowest in NE-trending axial portions of the Barcroft body, so it simply cooled inwards. Intrusion ~70 million years later by the McAfee Creek Granite had no discernable effect on δ¹⁸O values of Barcroft minerals and bulk rocks.     

Genesis of metapelitic migmatites in the Adirondack Mountains, New York

Oxygen isotope ratios and rare earth element (REE) concentrations provide independent tests of competing models of injection v. anatexis for the origin of migmatites from amphibolite and granulite facies metasedimentary rocks of the Adirondack Mountains, New York. Values of δ¹⁸O and REE profiles were measured by ion microprobe in garnet–zircon pairs from 10 sample localities. Prior U–Pb SIMS dating of zircon grains indicates that inherited cores (1.7–1.2 Ga) are surrounded by overgrowths crystallized during the Grenville orogenic cycle (～1.2–1.0 Ga). Cathodoluminescence imaging records three populations of zircon: (i) featureless rounded ‘whole grains’ (interpreted as metamorphic or anatectic), and rhythmically zoned (igneous) cores truncated by rims that are either (ii) discordant rhythmically zoned (igneous) or (iii) unzoned (metamorphic or anatectic). These textural interpretations are supported by geochronology and oxygen isotope analysis. In both the amphibolite facies NW Adirondacks and the granulite facies SE Adirondacks, δ¹⁸O_(Zrc) values in overgrowths and whole zircon are highly variable for metamorphic zircon (6.1–13.4‰; n = 95, 10 μm spot). In contrast, garnet is typically unzoned and δ¹⁸O_(Grt) values are constant at each locality, differing only between leucosomes and corresponding melanosomes. None of the analysed metamorphic zircon–garnet pairs attained oxygen isotope equilibrium, indicating that zircon rims and garnet are not coeval. Furthermore, REE profiles from zircon rims indicate zircon growth in all regions was prior to significant garnet growth. Thus, petrological estimates from garnet equilibria (e.g. P–T) cannot be associated uncritically with ages determined from zircon. The unusually high δ¹⁸O values (>10‰) in zircon overgrowths from leucocratic layers are distinctly different from associated metaigneous rocks (δ¹⁸O_(Zrc) < 10‰) indicating that these leucosomes are not injected magmas derived from known igneous rocks. Surrounding melanosomes have similarly high δ¹⁸O_(Zrc) values, suggesting that leucosomes are related to surrounding melanosomes, and that these migmatites formed by anatexis of high δ¹⁸O metasedimentary rocks.     

Oxygen Isotopic Study on the Date‐Nagai Skarn‐Type Tungsten Deposit,Northeastern Japan

The skarn‐type tungsten deposit of the Date‐Nagai mine is genetically related to the granodiorite batholith of the Iidateyama body. Skarn is developed along the contact between pelitic hornfels and marble that remains as a small roof pendant body directly above the granodiorite batholith. Zonal arrangement of minerals is observed in skarn. The zonation consists of wollastonite, garnet, garnet‐epidote, and vesuvianite‐garnet zones, from marble to hornfels. Sheelite is included in garnet, garnet‐epidote, and vesuvianite‐garnet zones. The oxygen isotope values of skarn minerals were obtained as δ¹⁸O = 4.2–7.7‰ for garnet, 5.9–6.9‰ for vesuvianite, ?0.3–3.4‰ for scheelite, 6.0–10.9‰ for quartz, and 8.2‰ for muscovite. The temperature of skarn‐formation was calculated from oxygen isotopic values of scheelite‐quartz pairs to be 288°C. Calculated oxygen isotope values of fluid responsible for skarn minerals were 6.1–9.5‰ for garnet, 1.2–4.8‰ for scheelite, ?1.3‐3.6‰ for quartz, and 4.5‰ for muscovite. Garnet precipitated from the fluids of different δ¹⁸O values from scheelite, quartz, and muscovite. These δ¹⁸O values suggest that the origin of fluid responsible for garnet was magmatic water, while evidence for the presence of a meteoric component in the fluids responsible for middle to later stages minerals was confirmed.     

Petrogenesis and tectonic implications of early Silurian high-K calc-alkaline granites and their potassic microgranular enclaves,western Kunlun orogen,NW Tibetan Plateau

The western Kunlun orogen occupies a key position along the tectonic junction between the Pan-Asian and Tethyan domains, reflecting Proto- and Palaeo-Tethys subduction and terrane collision during early Palaeozoic to early Mesozoic time. We present the first detailed zircon U–Pb chronology, major and trace element, and Sr–Nd–O–Hf isotope geochemistry of the Qiukesu pluton and its microgranular enclaves from this multiple orogenic belt. SHRIMP zircon U–Pb dating shows that the Qiukesu pluton was emplaced in the early Silurian (ca. 435 Ma). It consists of weakly peraluminous high-K calc-alkaline monzogranite and syenogranite, with initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7131–0.7229, ?_Nd(T) of –4.1 to –5.7, δ¹⁸O of 8.0–10.8‰, and ?_Hf(T) (in situ zircon) of –4.9. Elemental and isotopic data suggest that the granites formed by partial melting of lower-crustal granulitized metasedimentary-igneous Precambrian basement triggered by underplating of coeval mantle-derived enclave-forming intermediate magmas. Fractional crystallization of these purely crustal melts may explain the more felsic end-member granitic rocks, whereas such crustal melts plus additional input from coeval enclave-forming intermediate magma could account for the less felsic granites. The enclaves are intermediate (SiO₂ 57.6–62.2 wt.%) with high K₂O (1.8–3.6 wt.%). They have initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7132–0.7226, ?_Nd(T) of –5.0 to –6.0, δ¹⁸O of 6.9–9.9‰, and ?_Hf(T) (in situ zircon) of –8.1. We interpret the enclave magmas as having been derived by partial melting of subduction-modified mantle in the P–T transition zone between the spinel and spinel-garnet stability fields. Our new data suggest that subduction of the Proto-Tethyan oceanic crust was continuous to the early Silurian (ca. 435 Ma); the final closure of the Proto-Tethys occurred in the middle Silurian.     

Oxygen Isotopic Compositions of the Cape Ashizuri Granitoids in Southwest Japan

Oxygen isotopic composition was determined on representative samples of the Cape Ashizuri plutonic rocks, in order to estimate the genetic background of the biotite granite and alkaline granitoids. The biotite granite (70.1–76.1% SiO₂) ranged from 8.61 to 9.30‰ δ¹⁸O and averaged as 8.9‰ δ¹⁸O (n = 3), which is much smaller than the same Miocene granitoids of the Okueyama (avg. 10.1‰) and Takakumayama (11.6‰) granitic bodies, which are associated with tin mineralization. Among the alkaline granitoids, quartz syenites also have values as low as 7.14–8.70‰, with an average of 8.0‰ (n = 3), and monzonite and gabbro vary from 6.14 to 7.86‰, with an average of 7.0‰ (n = 3). These alkaline granitoids may be lower crustal in origin. The gabbroids containing 12.5% MgO at the maximum with low Sr initial ratio, are considered to be derived from the upper mantle through the fore‐arc tectonic break‐up on the subducting slab.     

Constraints from zircon U–Pb ages, O and Hf isotopic compositions on the origin of Neoproterozoic peraluminous granitoids from the Jiangnan Fold Belt, South China

Zircon textures and micro-chemical compositions precisely record the origin and petrogenesis of granitoids, which are crucial for evaluating crustal growth and reworking, thermal and geodynamic evolution. Zircons in peraluminous granitoids from the three largest 820 Ma complexes (Guibei, Yueyang and Jiuling) in the Jiangnan Fold Belt in South China are used to constrain their sources and petrogenetic processes. Zircons in the Guibei granitoids have complex internal structures. Nearly all magmatic and inherited zircons have similar εHf (?6.8 to +5.6) and δ¹⁸O values (8.8–11.6 ‰) and dominantly lie between εHf evolution vectors for a crust created between 1.7 and 2.1 Ga, suggesting that the Guibei granitoids were produced by partial melting of recycled heterogeneous supracrustal material. However, the Yueyang granitoids contain zircons with high εHf (?0.5 to +9.7) and relatively low δ¹⁸O values (5.9–8.4 ‰) and two-stage model ages of 1.1–1.8 Ga, and thus may have been formed by melting of mafic rocks from the lower crust. The Jiuling granitoids and their enclaves contain more complex zircons with more variable εHf (?7.2 to +9.7) and δ¹⁸O values (7.0–10.6 ‰), and lie along the mixing trend between the above-proposed infracrustal and supracrustal granitoids. Therefore, the Neoproterozoic peraluminous granitoids in the Jiangnan Fold Belt were produced by melting and mixing of continental crust. Compared with extremely low (≤4 ‰) and negative δ¹⁸O values of Neoproterozoic igneous zircons formed in its northern active continental margin, the high δ¹⁸O peraluminous granitoids in the southeastern Yangtze Block are considered to have been formed by melting of hydrothermally unaltered continental crust triggered by asthenosphere upwelling in the Nanhua back-arc basin.     

Protomylonite evolution potentially revealed by the 3D depiction and fractal analysis of chemical data from a feldspar

Tourmalinization associated with peraluminous granitic intrusions in metapelitic host-rocks has been widely recorded in the Iberian Peninsula, given the importance of tourmaline as a tracer of granite magma evolution and potential indicator of Sn-W mineralizations. In the Penamacor-Monsanto granite pluton (Central Eastern Portugal, Central Iberian Zone), tourmaline occurs: (1) as accessory phase in two-mica granitic rocks, muscovite-granites and aplites, (2) in quartz (±mica)-tourmaline rocks (tourmalinites) in several exocontact locations, and (3) as a rare detrital phase in contact zone hornfels and metapelitic host-rocks. Electron microprobe and stable isotope (δ¹⁸O, δD, δ¹¹B) data provide clear distinctions between tourmaline populations from these different settings: (a) schorl–oxyschorl tourmalines from granitic rocks have variable foititic component (^X□ = 17–57 %) and Mg/(Mg + Fe) ratios (0.19–0.50 in two-mica granitic rocks, and 0.05–0.19 in the more differentiated muscovite-granite and aplites); granitic tourmalines have constant δ¹⁸O values (12.1 ± 0.1 ‰), with wider-ranging δD (?78.2 ± 4.7 ‰) and δ¹¹B (?10.7 to ?9.0 ‰) values; (b) vein/breccia oxyschorl [Mg/(Mg + Fe) = 0.31–0.44] results from late, B- and Fe-enriched magma-derived fluids and is characterized by δ¹⁸O = 12.4 ‰, δD = ?29.5 ‰, and δ¹¹B = ?9.3 ‰, while replacement tourmalines have more dravitic compositions [Mg/(Mg + Fe) = 0.26–0.64], close to that of detrital tourmaline in the surrounding metapelitic rocks, and yield relatively constant δ¹⁸O values (13.1–13.3 ‰), though wider-ranging δD (?58.5 to ?36.5 ‰) and δ¹¹B (?10.2 to ?8.8 ‰) values; and (c) detrital tourmaline in contact rocks and regional host metasediments is mainly dravite [Mg/(Mg + Fe) = 0.35–0.78] and oxydravite [Mg/(Mg + Fe) = 0.51–0.58], respectively. Boron contents of the granitic rocks are low (<650 ppm) compared to the minimum B contents normally required for tourmaline saturation in granitic melts, implying loss of B and other volatiles to the surrounding host-rocks during the late-magmatic stages. This process was responsible for tourmalinization at the exocontact of the Penamacor-Monsanto pluton, either as direct tourmaline precipitation in cavities and fractures crossing the pluton margin (vein/breccia tourmalinites), or as replacement of mafic minerals (chlorite or biotite) in the host-rocks (replacement tourmalinites) along the exocontact of the granite. Thermometry based on ¹⁸O equilibrium fractionation between tourmaline and fluid indicates that a late, B-enriched magmatic aqueous fluid (av. δ¹⁸O ~12.1 ‰, at ~600 °C) precipitated the vein/breccia tourmaline (δ¹⁸O ~12.4 ‰) at ~500–550 °C, and later interacted with the cooler surrounding host-rocks to produce tourmaline at lower temperatures (400–450 °C), and an average δ¹⁸O ~13.2 ‰, closer to the values for the host-rock. Although B-metasomatism associated with some granitic plutons in the Iberian Peninsula seems to be relatively confined in space, extending integrated studies such as this to a larger number of granitic plutons may afford us a better understanding of Variscan magmatism and related mineralizations.     

Oxygen isotope and fluid inclusion study of the Sorkhe-Dizaj iron oxide-apatite deposit,NW Iran

The Sorkhe-Dizaj orebody is located 32 km southeast of Zanjan within the Tarom subzone of the Alborz-Azarbaijan structural zone. It is hosted mainly in quartz monzonite-monzodiorite and, to a lesser extent, in volcanoclastic rocks. Mineralization occurs in the form of stockwork and veins, comprising predominantly magnetite and actinolite, with minor pyrite and chalcopyrite. Two generations of magnetite and apatite are inferred: the first as disseminations in the host rock and the second mainly as an alteration product of actinolite, secondary K-feldspar, silica, sericite, chlorite and epidote. Fluid inclusion studies were carried out on second-generation apatite, and late-stage quartz to understand the geochemical evolution of the ore-bearing fluids. Fluid inclusions are of three types, i.e. primary, secondary, and pseudo-secondary. These inclusions are liquid or vapour single-phase, two-phase rich in liquid or vapour, and three-phase. Homogenization temperatures of second-generation apatite are inferred to be between 209°C and 520°C (mostly between 290°C and 320°C), indicating salinities of 9.08–21.61 wt.% NaCl equiv. At 342°C, the δ¹⁸O values range from 9‰ to 11.32‰ for the second-generation magnetite associated with coeval apatite. Fluid inclusions in the late-stage quartz veins are inferred to have homogenized between 186°C and 263°C, with δ¹⁸O values ranging between 2.5‰ and 7.4‰ at 220°C. Oxygen isotopes in the late-stage carbonate veins have values of 3.28–6.14‰ at 100°C. These data in the late-stage veins imply introduction of a cooler, less saline, isotopically depleted fluid, probably meteoric water. Field observations, mineral parageneses, and fluid inclusion?+?oxygen isotope data suggest that the magnetite-apatite veins formed from a predominantly magmatic-derived fluid. Introduction of cooler meteoric water in the final stage of mineralization reduced δ¹⁸O values, facilitating precipitation of sulphides, quartz, and carbonate veins.     

Polymetamorphism of the Chupa Sequence of the Belomorian mobile belt (Fennoscandia): Evidence from the isotope-geochemical (U-Pb,REE, O) study of zircon

U-Pb age and isotope-geochemical features were determined for zircon from kyanite gneisses and amphibolites of the Chupa Sequence of the Belomorian mobile belt (BMB) of the Fennoscandian shield. The cores of the zircon from the gneisses marks the Neoarchean events within 2700–2800 Ma known in the BMB, while those of the amphibolites correspond to the age of magmatic crystallization (2775 ± 12 Ma). The inner rims of zircon from the amphibolites and gneisses likely record two different Neoarchean metamorphic events (2650 ± 8 and 2599 ± 10 Ma, respectively). The outer rims record Paleoproterozoic metamorphism with an age of 1890 Ma, which formed the modern appearance and mineral assemblages of the rock association. The value of δ18O in the zircon from the gneiss is 8.6‰ in cores, slightly decreases to 8.0‰ in inner rims, and sharply decreases to 3.9‰ in outer rims. The value of δ¹⁸O in the zircon from the amphibolite is around 6.2‰ in cores, increases up to 8.6 in inner rims, and decreases to 5.2‰ in outer rims. A significant decrease of δ¹⁸O is likely related to the anomalous composition of Svecofennian metamorphic fluid restricted to local shear zones. The geochemical features of the zircons in combination with their morphology and anatomy make it possible to distinguish zircon generations of different age and change in metamorphic environments.     

Isotope geochemistry and geochronology of the Niujuan silver deposit,northern North China Craton: Implications for magmatism and metallogeny in an extensional tectonic setting

The Niujuan breccia-type silver deposit forms part of the North Hebei metallogenic belt along the northern margin of the North China Craton. The Hercynian Baiyingou coarse-grained granite and the Yanshanian Er’daogou fine-grained granite are the major Mesozoic intrusions exposed in this region. Here we investigate the salient characteristics of the mineralization and evaluate its genesis through zircon U-Pb and fluorite Sm-Nd age data, and Pb, S, O, H, He and Ar isotope data. The orebodies of the Niujuan silver deposit are hosted in breccias, which contain angular fragments of the Baiyingou and Er’daogou granitoids. The δ³⁴S values of pyrite from the silver mineralized veins range from 2.4‰ to 5.3‰. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios of the sulfide minerals show ranges of 16.837–16.932, 15.420–15.501 and 37.599–37.950, respectively. The ³He/⁴He and ⁴⁰Ar/³⁶Ar ratios of the fluids trapped in pyrite are 0.921–4.81Ra and 299.34–303.84, respectively. The δ¹⁸O and δ¹⁸D_w values of the ore-forming fluids range from 0.6‰ to −4.15‰ and from −119.4‰ to −98.7‰, respectively. Our isotopic data suggest that the ore-forming fluids were originally derived from the subvolcanic plutons and evolved into a mixture of magmatic and meteoric water during the main hydrothermal stage. The ore-forming materials were primarily derived from the lower crust with limited incorporation of mantle materials. The emplacement time of the Er’daogou granite is constrained by LA-ICP-MS zircon U-Pb geochronology at 145.5 ± 2.1 Ma. Five fluorite samples from the last hydrothermal stage yielded a Sm-Nd isochron age of 139.2 ± 3.8 Ma, indicating the upper age limit for the silver mineralization. These ages correlate with the formation of the Niujuan deposit in an extensional setting associated with the closure of the Mongol-Okhotsk Ocean and the subduction of the Paleo-Pacific oceanic plate beneath the North China Craton.     

Mineral compositions and fluid evolution of the Tonglushan skarn Cu–Fe deposit,SE Hubei,east-central China

The Tonglushan Cu–Fe deposit (1.12 Mt at 1.61% Cu, 5.68 Mt at 41% Fe) is located in the westernmost district of the Middle–Lower Yangtze River metallogenic belt. As a typical polymetal skarn metallogenic region, it consists of 13 skarn orebodies, mainly hosted in the contact zone between the Tonglushan quartz-diorite pluton (140 Ma) and Lower Triassic marine carbonate rocks of the Daye Formation. Four stages of mineralization and alterations can be identified: i.e. prograde skarn formation, retrograde hydrothermal alteration, quartz-sulphide followed by carbonate vein formation. Electron microprobe analysis (EMPA) indicates garnets vary from grossular (Ad_20.2–41.6Gr_49.7–74.1) to pure andradite (Ad_47.4–70.7Gr_23.9–45.9) in composition, and pyroxenes are represented by diopsides. Fluid inclusions identify three major types of fluids involved during formation of the deposit within the H₂O–NaCl system, i.e. liquid-rich inclusions (Type I), halite-bearing inclusions (Type II), and vapour-rich inclusions (Type III). Measurements of fluid inclusions reveal that the prograde skarn minerals formed at high temperatures (>550°C) in equilibrium with high-saline fluids (>66.57 wt.% NaCl equivalent). Oxygen and hydrogen stable isotopes of fluid inclusions from garnets and pyroxenes indicate that ore-formation fluids are mainly of magmatic-hydrothermal origin (δ¹⁸O = 6.68‰ to 9.67‰, δD = –67‰ to –92‰), whereas some meteoric water was incorporated into fluids of the retrograde alteration stage judging from compositions of epidote (δ¹⁸O = 2.26‰ to 3.74‰, δD= –31‰ to –73‰). Continuing depressurization and cooling to 405–567°C may have resulted in both a decrease in salinity (to 48.43–55.36 wt.% NaCl equivalent) and the deposition of abundant magnetite. During the quartz-sulphide stage, boiling produced sulphide assemblage precipitated from primary magmatic-hydrothermal fluids (δ¹⁸O = 4.98‰, δD = –66‰, δ³⁴S values of sulphides: 0.71–3.8‰) with an extensive range of salinities (4.96–50.75 wt.% NaCl equivalent), temperatures (240–350°C), and pressures (11.6–22.2 MPa). Carbonate veins formed at relatively low temperatures (174–284°C) from fluids of low salinity (1.57–4.03 wt.% NaCl equivalent), possibly reflecting the mixing of early magmatic fluids with abundant meteoric water. Boiling and fluid mixing played important roles for Cu precipitation in the Tonglushan deposit.     

Carbon and Oxygen Isotope Compositions of Calcite and Rhodochrosite from Geothermal Exploratory Drills TH‐4 and TH‐6 near the Toyoha Deposit,Hokkaido, Japan

We studied calcite and rhodochrosite from exploratory drill cores (TH‐4 and TH‐6) near the Toyoha deposit, southwestern Hokkaido, Japan, from the aspect of stable isotope geochemistry, together with measuring the homogenization temperatures of fluid inclusions. The alteration observed in the drill cores is classified into four zones: ore mineralized zone, mixed‐layer minerals zone, kaolin minerals zone, and propylitic zone. Calcite is widespread in all the zones except for the kaolin minerals zone. The occurrence of rhodochrosite is restricted in the ore mineralized zone associated with Fe, Mn‐rich chlorite and sulfides, the mineral assemblage of which is basically equivalent to that in the Toyoha veins. The measured δ¹⁸O_SMOW and δ¹³C_PDB values of calcite scatter in the relatively narrow ranges from ?2 to 5‰ and from ?9 to ?5‰, respectively; those of rhodochrosite from 3 to 9‰ and from ?9 to ?5‰, excluding some data with large deviations. The variation of the isotopic compositions with temperature and depth could be explained by a mixing process between a heated surface meteoric water (100°C δ¹⁸O =?12‰, δ¹³C =?10‰) and a deep high temperature water (300°C, δ¹⁸O =?5‰, δ¹³C =?4‰). Boiling was less effective in isotopic fractionation than that of mixing. The plots of δ¹⁸O and δ¹³C indicate that the carbonates precipitated from H₂CO₃‐dominated fluids under the conditions of pH = 6–7 and T = 200–300°C. The sequential precipitation from calcite to rhodochrosite in a vein brought about the disequilibrium isotopic fractionation between the two minerals. The hydrothermal fluids circulated during the precipitation of carbonates in TH‐4 and TH‐6 are similar in origin to the ore‐forming fluids pertaining to the formation of veins in the Toyoha deposit.