Geochronology and mineralogy of the Weishan carbonatite in Shandong province,eastern China

The Weishan REE deposit is located at the eastern part of North China Craton (NCC), western Shandong Province. The REE-bearing carbonatite occur as veins associated with aegirine syenite. LA-ICP-MS bastnaesite Th-Pb ages (129 Ma) of the Weishan carbonatite show that the carbonatite formed contemporary with the aegirine syenite. Based on the petrographic and geochemical characteristics of calcite, the REE-bearing carbonatite mainly consists of Generation-1 igneous calcite (G-1 calcite) with a small amount of Generation-2 hydrothermal calcite (G-2 calcite). Furthermore, the Weishan apatite is characterized by high Sr, LREE and low Y contents, and the carbonatite is rich in Sr, Ba and LREE contents. The δ¹³C_V-PDB (−6.5‰ to −7.9‰) and δ¹³O_V-SMOW (8.48‰–9.67‰) values are similar to those of primary, mantle-derived carbonatites. The above research supports that the carbonatite of the Weishan REE deposit is igneous carbonatite. Besides, the high Sr/Y, Th/U, Sr and Ba of the apatite indicate that the magma source of the Weishan REE deposit was enriched lithospheric mantle, which have suffered the fluid metasomatism. Taken together with the Mesozoic tectono-magmatic activities, the NW and NWW subduction of Izanagi plate along with lithosphere delamination and thinning of the North China plate support the formation of the Weishan REE deposit. Accordingly, the mineralization model of the Weishan REE deposit was concluded: The spatial-temporal relationships coupled with rare and trace element characteristics for both carbonatite and syenite suggest that the carbonatite melt was separated from the CO₂-rich silicate melt by liquid immiscibility. The G-1 calcites were crystallized from the carbonatite melt, which made the residual melt rich in rare earth elements. Due to the common origin of G-1 and G-2 calcites, the REE-rich magmatic hydrothermal was subsequently separated from the melt. After that, large numbers of rare earth minerals were produced from the magmatic hydrothermal stage.     

U-Pb zircon geochronology, geochemistry and kinetics of the Huaniushan A-type granite in Northwest China

The Huaniushan granite is located at the Beishan orogenic belt, northwestern China. At the contact zone between the granite and marble, a hydrothermal Pb-Zn and skarn Au deposit is formed. LA-ICP-MS zircon U-Pb dating yielded a weighted mean 206Pb/238U age of 229.5±2.6 Ma (MSDW=0.93) for the Huaniushan granite, imply-ing its Late Triassic intrusion. Geochemistry analyses show that the Huaniushan granite is enriched in Si, K, Na, and REE, and depleted in Mg and Ca, with contents of SiO2 (70.8% to 74.4%), Na2O+K2O (8.8% to 10.2%), CaO (0.93% to 1.44%), and MgO (0.14% to 0.48%). REE is characterized by obvious negative Eu anomaly. Rb, Th, U, K, Pb, Nb, Zr and Hf elements are rich in the granite while Ba, Sr, P, Ti and Eu are deplete. The granite has a high (Zr+Nb+Ce+Y) abundance and 104 Ga/Al ratios. Petrology, major and trace elements data all indicate that the Hua-niushan granite is A-type granite which intruded in a post-collisional extensional tectonic setting. The magma was dominantly sourced from partial melting of crustal intermediate-felsic igneous rocks. Intensive magmatic activities and Au-Cu-Mo mineralization occurred throughout the Beishan orogenic belt during the period from ca. 240 to 220 Ma.     

Characteristic Features of REE and Pb–Zn–Ag Mineralizations in the Na Son Deposit,Northeastern Vietnam

The Na Son deposit is a small‐scale Pb–ZnPb–Zn–Ag deposit in northeast Vietnam and consists of biotite–chlorite schist, reddish altered rocks, quartz veins and syenite. The biotite–chlorite schist is intruded by syenite. Reddish altered rocks occur as an alteration halo between the biotite–allanite‐bearing quartz veins and the biotite–chlorite schist. Allanite occurs in the biotite–allanite‐bearing quartz veins and in the proximal reddish altered rocks. Rare earth element (REE) fluorocarbonate minerals occur along fractures or at rim of allanite crystals. The later horizontal aggregates of sulfide veins and veinlets cut the earlier reddish altered rocks. The earlier Pb–Zn veins consist of a large amount of galena and lesser amounts of sphalerite, pyrite and molybdenite. The later Cu veins cutting the Pb–Zn veins include chalcopyrite and lesser amounts of tetrahedrite and pyrite. The occurrences of two‐phase H₂O–CO₂ fluid inclusions in quartz from biotite–allanite‐bearing quartz veins and REE‐bearing fluorocarbonate minerals in allanite suggest the presence of CO₂ and F in the hydrothermal fluid. The oxygen isotopic ratios of the reddish altered rocks, biotite–chlorite schist, and syenite range from +13.9 to +14.9 ‰, +11.5 to +13.3 ‰, and +10.1 to +11.6 ‰, respectively. Assuming an isotopic equilibrium between quartz (+14.6 to +15.8 ‰) and biotite (+8.6 ‰) in the biotite–allanite‐bearing quartz vein, formation temperature was estimated to be 400°C. At 400°C, δ¹⁸O values of the hydrothermal fluid in equilibrium with quartz and biotite range from +10.5 to +11.7 ‰. These δ¹⁸O values are consistent with fluid that is derived from metamorphism. Assuming an isotopic equilibrium between galena (+1.5 to +1.7 ‰) and chalcopyrite (+3.4 ‰), the formation temperature was estimated to be approximately 300°C. The formation temperature of the Na Son deposit decreased with the progress of mineralization. Based on the geological data, occurrence of REE‐bearing minerals and oxygen isotopic ratios, the REE mineralization is thought to result from interaction between biotite–chlorite schist and REE‐, CO₂‐ and F‐bearing metamorphic fluid at 400°C under a rock‐dominant condition.     

The world-class Natalka gold deposit, northeast Russia: REE patterns, fluid inclusions, stable oxygen isotopes, and formation conditions of ore

REE patterns of hydrothermally altered rocks, fluid inclusions, and stable oxygen isotopes of quartz were studied at the Natalka gold deposit. Metasomatic rocks formed under decompression reveal gradual depletion in LREE and HREE relative to siltstone of the protolith. The HREE patterns of metasomatic rocks formed under decompression are uniform; an insignificant removal of LREE can be noted. The progressive extraction of REE with increasing alteration of rocks could have been due to the effect of magmatogenic or meteoric fluid. Because a Ce anomaly is absent, the participation of oxidized meteoric water was limited. The inverse correlation between the total REE content and the Eu anomaly value in altered rocks indicates a substantial role of magmatogenic fluid. The REE patterns of altered rocks formed under compression show that the role of metamorphic fluid was not great. All metasomatic rocks are enriched in LREE, so that the enrichment of fluid in LREE as well may be suggested. Three fluid compositions were captured as fluid inclusions: (1) H₂O-CO₂-NaCl-MgCl₂ with a salinity of 1.0–4.9 wt % NaCl equiv, (2) CO₂-CH₄, and (3) H₂O-NaCl-MgCl₂ with a salinity of 7.0–5.6 wt % NaCl equiv. Compositions (1) and (2) coexisted in the mineral-forming system at 250–350°C and 1.1–2.4 kbar as products of phase separation under conditions of decreasing P and T. The interaction of this fluid with host rocks resulted in the formation of extensive halos of beresitized rocks with sulfide disseminations. The precipitation of arsenopyrite and pyrite led to the substantial depletion of mineral-forming fluid in H₂S and destabilization of the Au(HS)^2? complex. The fluid with the third composition arose due to the boiling of the H₂O-CO₂-CH₄-NaCl-MgCl₂ liquid and was responsible for metasomatic alteration of host rocks. The late mineral assemblages were deposited from this fluid at the initial stage of ore formation. The high methane concentrations in the ore-forming fluid were likely caused by interaction of hydrothermal ore-bearing solutions with carbonaceous host rocks. The δ¹⁸O values of quartz from quartz-scheelite-pyrite-arsenopyrite and sulfide-sulfosalt mineral assemblages vary from +11.6 to +14.1‰ and +11.2 to +13.5‰, respectively. The parental fluids of the early and late mineral assemblages probably were derived from a magmatic source and were characterized by $ \delta ^{18} O_{H_2 O} REE patterns of hydrothermally altered rocks, fluid inclusions, and stable oxygen isotopes of quartz were studied at the Natalka gold deposit. Metasomatic rocks formed under decompression reveal gradual depletion in LREE and HREE relative to siltstone of the protolith. The HREE patterns of metasomatic rocks formed under decompression are uniform; an insignificant removal of LREE can be noted. The progressive extraction of REE with increasing alteration of rocks could have been due to the effect of magmatogenic or meteoric fluid. Because a Ce anomaly is absent, the participation of oxidized meteoric water was limited. The inverse correlation between the total REE content and the Eu anomaly value in altered rocks indicates a substantial role of magmatogenic fluid. The REE patterns of altered rocks formed under compression show that the role of metamorphic fluid was not great. All metasomatic rocks are enriched in LREE, so that the enrichment of fluid in LREE as well may be suggested. Three fluid compositions were captured as fluid inclusions: (1) H₂O-CO₂-NaCl-MgCl₂ with a salinity of 1.0–4.9 wt % NaCl equiv, (2) CO₂-CH₄, and (3) H₂O-NaCl-MgCl₂ with a salinity of 7.0–5.6 wt % NaCl equiv. Compositions (1) and (2) coexisted in the mineral-forming system at 250–350°C and 1.1–2.4 kbar as products of phase separation under conditions of decreasing P and T. The interaction of this fluid with host rocks resulted in the formation of extensive halos of beresitized rocks with sulfide disseminations. The precipitation of arsenopyrite and pyrite led to the substantial depletion of mineral-forming fluid in H₂S and destabilization of the Au(HS)²⁻ complex. The fluid with the third composition arose due to the boiling of the H₂O-CO₂-CH₄-NaCl-MgCl₂ liquid and was responsible for metasomatic alteration of host rocks. The late mineral assemblages were deposited from this fluid at the initial stage of ore formation. The high methane concentrations in the ore-forming fluid were likely caused by interaction of hydrothermal ore-bearing solutions with carbonaceous host rocks. The δ¹⁸O values of quartz from quartz-scheelite-pyrite-arsenopyrite and sulfide-sulfosalt mineral assemblages vary from +11.6 to +14.1‰ and +11.2 to +13.5‰, respectively. The parental fluids of the early and late mineral assemblages probably were derived from a magmatic source and were characterized by = +6.3 to +8.8‰ at 350°C and +3.6 to +5.9‰ at 280°C, respectively. The narrow interval of oxygen isotopic compositions shows that this source was homogeneous. The data obtained allow us to suggest that the deposit formation was related to magmatic activity, including the direct supply of ore components from a magma chamber and mobilization of these components in the processes of dehydration and decarbonation during contact and regional metamorphism. Original Russian Text ? N.A. Goryachev, O.V. Vikent’eva, N.S. Bortnikov, V.Yu. Prokof’ev, V.A. Alpatov, V.V. Golub, 2008, published in Geologiya Rudnykh Mestorozhdenii, 2008, Vol. 50, No. 5, pp. 414–444.     

Stable isotope evidence for magmatic fluid input during large-scale Na–Ca alteration in the Cloncurry Fe oxide Cu–Au district, NW Queensland, Australia

Sodic–calcic alteration is common in mineralized hydrothermal systems, yet the relative importance of igneous vs. basinal fluid sources remains controversial. One of the most extensive volumes of sodic–calcic rocks occurs near Cloncurry, NW Queensland, and was formed by overlapping hydrothermal systems that were active synchronously with emplacement of mid‐crustal batholithic granitoids (c. 1.55–1.50 Ga). Altered rocks contain albite–oligoclase, actinolite, diopside, titanite and magnetite. Alteration was localized by: (A) composite veins and breccias containing crystallized magma intimately intergrown with hydrothermal precipitates; (B) intrusions that host setting A veins and breccias; and (C) extensive breccia and vein systems linked to regional fault systems. Isotope analyses of actinolites in settings A and B indicate calculated δ¹⁸O_H2O (+8.2 to +10.6‰) and variably depleted δD_H2O (?130 to ?54‰) compared with typical magmatic fluids, whereas those from setting C typically indicate calculated δ¹⁸O_H2O (+8.0 to +12.8‰) and δD_H2O (?29 to ?99‰). The lowest δD_H2O values are interpreted as representing residual fluids after significant (> 90%) open‐system magmatic degassing. Overall the stable isotope, field, geochronological and geobarometric data suggest that these sodic–calcic alteration systems were formed by the episodic incursion of magmatic fluids that underwent minor isotopic modification as a result of varying degrees of interaction with country rocks.     

Stable isotope compositions of tourmalines from granites and related hydrothermal rocks of the Karagwe-Ankolean belt,northwest Tanzania

Tourmaline is a ubiquitous mineral in the Mid-Proterozoic, peraluminous, syn- to post-tectonic granites and aplites and the related hydrothermal rocks of the Karagwe-Ankolean belt in northwest Tanzania. Electron microprobe analysis indicates that tourmalines from all of the intrusive and hydrothermal lithologies: (1) belong to the schorl-dravite solid-solution series; and (2) plot within the field occupied by tourmaline from Li-poor granitoids on the Fe-Al-Mg classification diagram. Oxygen isotope compositions range from +12.2 to +11.6‰ (SMOW) for magmatic tourmalines and from +10.8 to +9.8‰ for those of hydrothermal origin. Hydrogen isotope compositions vary from −79 to − 65‰ (SMOW) for magmatic tourmalines and from −99 to −84‰ for hydrothermal tourmalines. Water contents measured by manometry are constant at 3.0–3.2 wt.%. Within the broad grouping there arc systematic variations in both chemical [particularly Fe_tot/(Fe_tot + Mg ratio)] and isotopic composition that relate to evolving magmatic and hydrothermal conditions. Igneous differentiation [increasing Fe_tot/(Fe_tot + Mg) in magmatic tourmaline] has produced trends with higher δ¹⁸O in quartz, lower δ¹⁸O in tourmaline, and larger Δ_QTZ.−TOUR.-values, that reflect a combination of a reduction of crystallization temperature and an increase of Fe_tot/ (Fe_tot + Mg) in the residual melt. Subsequent cooling and interaction of an exsolved, B-rich magmatic fluid with the pelitic country rocks, resulted in the deposition of hydrothermal tourmaline with increasing Fe_tot/(Fe_tot + Mg) ratios, and progressively lower δ¹⁸O and δD -values.     

Geochemistry of granitization and magmatic replacement of basic volcanic rocks in the contact aureole of the Yurchik gabbronorite intrusion, Ganal Range, Kamchatka

Geological and geochemical data indicate that the formation of the granulite-like rocks in the contact aureole of the Yurchik gabbronorite intrusion of the Ganal Range, Kamchatka, was caused by the contact metamorphism, metasomatism, and local melting of the initial volcanosedimentary rocks of the Vakhtalka Sequence of the Ganal Group. The temperature in the inner part of the aureole reached 700–800°C and caused the transformation of the basic volcanic rocks of the sequence into two pyroxene-plagioclase, clinopyroxene-amphibole-plagioclase, and amphibole-plagioclase hornfelses, while sedimentary rocks were converted into garnet-biotite ± cordierite hornfelses. The hornfelsed basic volcanic rocks were locally subjected to metasomatic alteration and magmatic replacement with formation of biotite-orthopyroxene-plagioclase metasomatic bodies containing biotite-orthopyroxene-plagioclase ± garnet veinlets and aggregates. During these processes, sedimentary interlayers were converted into garnet enderbites at 700–800°C and 3.2–4.8 kbar. The comparison of the chemical composition of basic volcanic rocks of the Vakhtalka Sequence and their transformation products indicates that the metasomatic alteration and magmatic replacement correspond to siliceous-alkaline metasomatism (granitization) and cause subsequent and uneven influx of SiO₂, Al₂O₃, Na₂O, K₂O, Rb, Ba, Zr, Nb, and Cl and removal of Fe, Mg, Mn, Ca, Cr, Co, Ti, Y, and S. REE data on basic metavolcanic rocks, hornfelses, and metasomatites suggest that the processes of hornfelsation, metasomatism, and magmatic replacement of the initial volcanic rocks were accompanied by significant increase in LREE and slight decrease in HREE. The Sr and Nd isotope study of the rocks in the aureole showed that the initial basic volcanic rocks of the Vakhtalka Sequence are isotopically close to both mature island arc tholeiites and mid-ocean ridge basalts. The metasomatic alteration and magmatic replacement of volcanic rocks in the aureole lead to the decrease of ¹⁴³Nd/¹⁴⁴Nd and increase of ⁸⁷Sr/⁸⁶Sr approximately parallel to mantle array. Pb isotopic ratios in the studied rocks become more radiogenic from initial metavolcanic rocks to metasomatites. It is suggested that the processes of metamorphism, metasomatism, and magmatic replacement were caused by highly mineralized mantle fluids, which percolated along magmatic channels serving as pathways for gabbroid magma.     

Geochemistry of granulite‐facies granitic rocks from Battye Glacier,northern Prince Charles Mountains,East Antarctica

Proterozoic basement outcrops in the vicinity of Battye Glacier, northern Prince Charles Mountains, are dominated by granulites and gneisses derived from felsic (granitoid) intrusive igneous rocks, and by pegmatites. Felsic orthopyroxene granulites, garnet leucogneisses and garnet pegmatites have major and trace element compositions of highly felsic, but not strongly fractionated, granites. The garnet leucogneisses and garnet pegmatites have S‐type characteristics, whereas the felsic granulites are probably I‐type, although their high Zr+Nb+Y+Ce abundances suggest possible A‐type affinities. Intermediate orthopyroxene ± clinopyroxene granulites mostly resemble I‐type quartz diorites, except for a small subgroup of samples (characterised by low Na₂O and K₂O, and high MgO, Ni, Cr and HREE) of uncertain affinities and significance. Element ratios involving LILE (e.g. K/Rb, Rb/Ba, Rb/Sr, K/La, La/Th) closely match those typical of the inferred granitoid protoliths, suggesting that these rocks have experienced relatively little LILE depletion (except possibly for U) during regional metamorphism. It is therefore inferred that metamorphism was probably broadly isochemical. Because the felsic and intermediate granulites and garnet leucogneisses are Sr‐depleted, Y‐undepleted and mostly have negative Eu anomalies they are inferred to be the products of partial melting of felsic crustal sources leaving plagioclase‐bearing residua. Plagioclase fractionation during crystallisation could also account for these characteristics, but K/Rb, Rb/Ba and Rb/Sr ratios in these rocks are not consistent with strong fractionation of feldspar. Garnet pegmatites differ chemically from garnet leucogneisses mainly in their lower Fe, Ti, Nb, Zn, Zr, Th and REE abundances and positive Eu anomalies, related to lower garnet, ilmenite and zircon contents in the garnet pegmatites. A genetic link between these two rock types, probably involving fractionation of these minerals during partial melting or crystallisation, is inferred. Incompatible‐element abundances suggest that generation of the Battye Glacier granitic magmas from felsic crust might have occurred in a mature continental magmatic arc possibly well removed from an active subduction trench or, perhaps, in an intracontinental setting.     

Metasomatism of a depleted granulite facies terrain in the Arunta Block,central Australia

Geochemical investigations in the Utralanama Block, an intermediate pressure granulite facies terrain in the Arunta Block, central Australia, has revealed several anomalous features, not consistent with the depletion of granitophile components generally considered to accompany granulite facies metamorphism. However, other geochemical features are indicative of depletion. The mean K₂O for the Utralanama Block is exceptionally low relative to most other granulite facies terrains, but Rb contents are comparatively high. Consequently, the mean K/Rb ratio is relatively low for granulite facies terrains as is the mean Ba/Rb ratio, whilst mean K/Sr and Rb/Sr ratios are much higher than usual for such terrains. Only the K/Ba ratio shows equivalent values to depleted terrains elsewhere.Comparison of these ratios for the three main compositional groups of rocks in the Utralanama Block reveals that for mafic rocks all the above ratios are characteristic of extreme depletion, whereas, for all but the K/Ba ratio, mean ratios for the pelitic rocks, and to a lesser extent for the quartzofeldspathic rocks approach normal crustal values or values for metasomatic rocks. The abnormally high Rb/Sr ratios of these rocks compared to average crustal rocks suggest, however, that metasomatism is the cause of the anomalous geochemical features of the Utralanama Block, and this is supported by field and microstructural evidence. Thus, Rb/Sr ratios appear to be useful indicators of metasomatism where no gross mineralogical or microstructural evidence for metasomatism is obvious, and under such conditions the K/Ba ratio may be more reliable than the K/Rb ratio for indicating prior depletion of the terrain.     

Genesis and formation conditions of deposits in the unique Strel’tsovka Molybdenum-Uranium ore field: New mineralogical,geochemical, and physicochemical evidence

The ambiguity of genetic interpretations of uranium ore formation at Mo-U deposits of the Strel’tsovka ore field led us to perform additional geochemical, mineralogical, and thermobarogeochemical studies. As a result, it has been established that closely related U and F were progressively gained in the Late Mesozoic volcanic rocks from the older basic volcanics (170 Ma) to the younger silicic igneous rocks (140 Ma). The Early Cretaceous postmagmatic hydrothermal epoch (140–125 Ma) is subdivided into preore, uranium ore, and first and second postore stages. The primary brannerite-pitchblende ore was formed in association with fluorite. At the first postore stage, this assemblage was replaced by a U-Si metagel, which was previously identified as coffinite. The metagel shows a wide compositional variation; its fine structure has been studied. The preore metasomatic alteration and related veined mineralization were formed under the effect of sodium (bicarbonate)-chloride solution at a temperature of 250–200°C. The uranium ore formation began with albitization and hematitization of rocks affected by supercritical fluid at 530–500°C; brannerite and pitchblende precipitated at 350–300°C. The chondrite-normalized REE patterns of pitchblende hosted in trachybasalt, trachydacite, and granite demonstrate a pronounced Sm-Nd discontinuity and a statistically significant tetrad effect of W type. These attributes were not established in REE patterns of rhyolites derived from the upper crustal magma chamber. This circumstance and a chronological gap of 5 Ma between silicic volcanism and ore formation do not allow us to suggest that uranium was derived from this magma chamber. According to the proposed model, the evolved silicic Li-F magma was a source of uranium. U⁴⁺, together with REE, was fractionated into the fluid phase as complex fluoride compounds. The uranium mineralization was deposited at a temperature barrier. It is suggested that hydromica alteration and the formation of molybdenum mineralization were genetically unrelated to the uranium ore formation.     

Chronology of hydrothermal and magmatic activity in the Dukat gold-silver ore field

The previously published and newly obtained geological and geochronological (Rb-Sr and Ar-Ar) data show that the igneous rocks and products of hydrothermal alteration in the Dukat ore field pertain to two ore-forming magmatic-hydrothermal systems (OMHSs). The igneous rocks of the Early Cretaceous rift-related OMHS are represented by potassium rhyolites of the Askol’d Formation with Rb-Sr ages of 124 ± 3 and 119.3 ± 3.4 Ma and intercalating amygdaloidal basalts. The products of the hydrothermal activity of this OMHS are the metasomatic anatase-chlorite assemblage of the root zone, which replaces potassium rhyolites, and shallow-seated quartz-adularia and quartz-carbonate-feldspar veinlets retained in rhyolite fragments in Late Cretaceous conglomerate and breccia. The Late Cretaceous OMHS was related to the origination of the Okhotsk-Chukotka volcanic belt and consists of calc-alkaline basaltic andesites of the Tavvatum Formation and moderately silicic K-Na rhyolites of the Nayakhan Formation with a Rb-Sr age of 84 ± 4 Ma. The Late Cretaceous postmagmatic hydrothermal activity in the Dukat ore field resulted in the formation of preore metasomatic rocks and orebodies of the unique Dukat Au-Ag deposit. The first stage of the Late Cretaceous hydrothermal activity gave birth to preore propylites with a Rb-Sr isochron age of adularia samples estimated at 85 ± 1 Ma and quartz-chlorite-sulfide and Ag-bearing quartz-chlorite-adularia orebodies with Rb-Sr isochron ages of adularia estimated at 84 ± 1 and 86.1 ± 4 Ma. The second stage was marked by the formation of garnet-bearing propylites and quartz-rhodonite orebodies with a Rb-Sr age of 73 ± 3 Ma. Further hydrothermal activity occurred after a break related to structural rearrangement of the ore field and was expressed in the replacement of propylites by products of argillin alteration and Ag-bearing Mn hydroxides. Paleogene basaltic dikes and related subeconomic mineralization concluded magmatic and hydrothermal processes in the Dukat ore field.     

Geochemical characteristics of iron ore deposits in central eastern Turkey: an approach to their genesis

ABSTRACT

Economically the most important iron deposits of Turkey occur as: (1) skarn-hosted (SH)-type ore deposits, occurring along the contacts between syenitic-monzonitic intrusives and limestone or serpentine; (2) vein-type deposits, found between the serpentine and limestone (SLH); or (3) ore deposits that are entirely within the limestone (LH).

Elemental associations are defined as: Fe+Ni+Cr+U+Bi+Rb+Mg+Ga for the SH-type ores; Fe+Cr+Mn+Nb+V for the SLH-type ores; and Fe+Ag+Au+Cr+Ba+As+Pb+Sb+Ni for the LH-type ores. Positive correlations between Fe, U, Bi, and Rb for the SH type indicate that late magmatic hydrothermal input was related to monzonitic intrusions. Chondrite-normalized rare earth element (REE) patterns of the 14 deposits show very weak light/heavy REE (LREE/HREE) fractionation. Similarities of REE patterns, particularly between the SH and LH types, may indicate a common source of REEs and Fe. Ce depletion in the LH ores indicates long-term fluid flow and interaction with marine sediments. Ni, Cr, and V enrichment of all deposits indicates that iron was scavenged from the serpentinized ultra-basic-basic rocks and transported along fracture zones by hydrothermal solutions driven by intrusions. The iron deposits were formed around the magmatic bodies, or tectonic contacts between the serpentine and the limestone.     

Rubidium Isotope Ratios of International Geological Reference Materials

In this study we determined rubidium isotope ratios in twenty-one commonly used international geological reference materials, including igneous, sedimentary and metamorphic rocks, as well as an IAPSO seawater reference material. All δ⁸⁷Rb results were obtained relative to the NIST SRM 984 reference material. For most reference materials, Rb was purified using a single column loaded with Sr-spec resin. For reference materials containing low Rb but high mass fractions of matrix elements (such as basic rock and seawater), Rb was purified using two-column chromatography, with the first column packed with AGMP-50 resin and the second column packed with Sr-spec resin. Two methods for instrumental mass bias correction, sample-standard bracketing (SSB) mode, and the combined sample-standard bracketing and Zr internal normalisation (C-SSBIN) method, were compared for Rb isotopic measurements by multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). The long-term reproducibility of Rb isotopic measurements using both methods was similar, better than 0.06‰ (2s, standard deviation) for NIST SRM 984. Significant Rb isotopic fractionation was observed among the reference materials, with an overall variation in δ⁸⁷Rb values of approximately 0.5‰. The δ⁸⁷Rb values of igneous rocks ranged from -0.28‰ to +0.06‰, showing a trend from heavier isotopic compositions in mafic rocks to lighter δ⁸⁷Rb values in the more evolved felsic rocks. The sedimentary and metamorphic rocks had Rb isotope ratios similar to those of igneous rocks. The δ⁸⁷Rb values of the reference materials related to low-temperature geological processes showed a wider range than those of high-temperature processes. Notably, the IAPSO seawater reference material had a δ⁸⁷Rb value of +0.14‰, which deviated from that of igneous rocks, and represents the heaviest reservoir of Rb isotopes found thus far on Earth. The comprehensive dataset presented here has the potential to serve for quality assurance purposes, and provide a framework for interlaboratory comparisons of Rb isotope ratios.     

Geochemistry and petrogenesis of acid volcano-plutonic rocks of the Siner area, Siwana Ring Complex, Northwestern Peninsular India

Petrochemical studies on acid plutonic (granite, microgranite) and volcanic (rhyolite, trachyte) rocks occurring in the Siner area of the Siwana Ring Complex, Malani Igneous Suite have been carried out. These rocks are characterized by high concentrations of SiO₂, Na₂O, K₂O, Zr, Nb, Y and REE (except Eu) but low in MgO, Fe₂O₃(t), CaO, Cr, Ni, Sr; indicating their A-type affinity. Field studies in conjunction with the geochemical characteristic indicate that the magmatism in the Siner area is generally represented by peralkaline suite of rocks which are formed due to rift tectonics. It is also suggested that these acidic rocks could have been derived by low degree partial melting of crustal material. Characteristics of certain pathfinder elements such as Rb, Ba, Sr, K, Zr, Nb, REE and the ratios of K/Rb, Zr/Rb, Ba/Rb along with the multi elemental primitive mantle normalized spidergrams suggest that the Siner peralkaline granites and microgranites have the potential for rare metal and rare earth mineralizations.     

The Northeast Kingdom batholith,Vermont: magmatic evolution and geochemical constraints on the origin of Acadian granitic rocks

Five Devonian plutons (West Charleston, Echo Pond, Nulhegan, Derby, and Willoughby) that constitute the Northeast Kingdom batholith in Vermont show wide ranges in elemental abundances and ratios consistent with major crustal contributions during their evolution. The batholith consists of metaluminous quartz gabbro, diorite and quartz monzodiorite, peraluminous granodiorite and granite, and strongly peraluminous leucogranite. Contents of major elements vary systematically with increasingSiO<₂ (48 to 77 wt.%). The batholith has calc-alkaline features, for example a Peacock index of 57, and values for K<₂O/Na₂O (<1), K/Rb (60–350), Zr/Hf (30–50), Nb/Ta (2–22), Hf/Ta (up to 10), and Rb/Zr (<2) in the range of plutonic rocks found in continental magmatic ares. Wide diversity and high values of minor- and trace-element ratios, including Th/Ta (0.5–22), Th/Yb (0–27), Ba/La (0–80), etc., are attributed to intracrustal contributions. Chondrite-normalized REE patterns of metaluminous and relatively mafic intrusives have slightly negative slopes (La/Yb_cn<10) and negative Eu anomalies are small orabsent. The metaluminous to peraluminous inter-mediate plutons are relatively enriched in the light REE (La/Yb_cn>40) and have small negative Eu anomalies. The strongly peraluminous Willoughby leucogranite has unique trace-element abundances and ratios relative to the rest of the batholith, including low contents of Hf, Zr, Sr, and Ba, low values of K/Rb (80–164), Th/Ta (<9), Rb/Cs (7–40), K/Cs (0.1–0.5), Ce/Pb (0.5–4), high values of Rb/Sr (1–18) low to moderate REE contents and light-REE enriched patterns (with small negative Eu anomalies). Flat REE patterns (with large negative Eu anomalies) are found in a small, hydrothermally-altered area characterized by high abundances of Sn (up to 26 ppm), Rb (up to 670 ppm), Li (up to 310 ppm), Ta (up to 13.1 ppm), and U (up to 10 ppm). There is no single mixing trend, fractional crystallization assemblage, or assimilationscheme that accounts for all trace elementvariations from quartz gabbro to granite in the Northeast Kingdom batholith. The plutons originated by mixing mantle-derived components and crustal melts generated at different levels in the heterogeneous lithosphere in a continental collisional environment. Hybrid rocks in the batholith evolved by fractional crystallization and assimilation of country rocks (<50% by mass), and some of the leucogranitic rocks were subsequently disturbed by a mild hydrothermal event that resulted in the deposition of small amounts of sulfide minerals.     

岩浆(型)碳酸岩研究进展

主要从岩石学，矿物学，岩石分类，C，O，Sr同位素，碳酸岩与矿化的关系等各方面对（碱性）碳酸岩的研究进行了较为全面的总结，并结合近20年来实验岩石等，流体包裹体研究，CO2^- H2O－NaCl流体体系的性质的研究，对碳酸岩岩浆的来源及成因，岩浆－热液的演化进行了分析和探讨，碳酸岩形成至少经历了三个阶段，即岩浆阶段，岩浆期后阶段（气相碳酸岩／岩浆热液阶段），交代碳酸岩阶段，而作为与碳酸岩在空间和成因上有密切联系的基性，超基性岩，碱性岩杂岩体，则经历了碳酸岩成岩阶段以前的岩浆不混熔作用，结晶分异作用，岩浆结晶作用以及碳酸岩形成之后的围岩蚀变（霓长岩化）作用。     

Iron isotope, major and trace element characterization of early Archean supracrustal rocks from SW Greenland: Protolith identification and metamorphic overprint

The iron isotope, trace and major element compositions of Eoarchean supracrustal rocks from southern West Greenland (Isua Supracrustal Belt, the islands of Akilia and Innersuartuut) were analyzed in order to identify protoliths and characterize the imprints of metamorphism and metasomatism. Banded iron formations (BIFs) from the Isua Supracrustal Belt (ISB) have trace element characteristics that are consistent with seawater derivation, including high Y/Ho ratios, positive Eu/Eu^∗ anomalies, positive La/La^∗ anomalies, and concave upward REE patterns. These rocks also have heavy Fe isotopic compositions relative to surrounding igneous rocks (∼+0.4‰/amu). The most likely interpretation is that this signature was inherited from partial oxidation in a marine setting of Fe emanating from a source similar to modern mid-ocean ridge hydrothermal vents (∼−0.15‰/amu).Banded quartz-rich rocks from the island of Akilia with high Fe/Ti ratios share many similarities with bona fide BIFs from Isua (heavy Fe isotopic compositions up to +0.4‰/amu, elevated Y/Ho ratios compared to igneous rocks, sometimes positive Eu/Eu^∗ anomalies) suggesting a chemical sedimentary origin.Iron-poor metacarbonates from the southwestern part of the ISB have light Fe isotopic compositions (∼−0.4‰/amu). This is consistent with derivation of these rocks by fluid flow through surrounding ultramafic rocks and deposition as metasomatic carbonates. Iron-rich metacarbonates from the northwest and northeast parts of the ISB have Fe isotopic compositions (from +0.1 to +0.4‰/amu) and trace element patterns (high Y/Ho ratios, positive Eu/Eu^∗ and La/La^∗ anomalies, and concave upward REE) similar to associated BIFs. The most likely interpretation is that these iron-rich metacarbonates were derived from mobilization of Fe in BIFs by metasomatic fluids.     

Petrology,geochemistry and geochronology of the Chilka Lake igneous complex,Orissa state,India

The Chilka Lake igneous complex of Orissa, the largest known anortosite massif of the Indian Shield, occurs in a catazonal environment of high-grade metamorphics of the Eastern Ghats Precambrian Orogenic Province. The syntectonic massif consists of the anorthositic Balugaon dome, leuconoritic Rambha lobe and quartz-mangeritic Kallikota cover. A completely gradational suite comprising anorthosite-leuconorite-norite-minor jotunite (the anorthositic suite) constitutes most of the complex. The subordinate of suite of acid rocks spatially associated with this is of a broad quartz-mangeritic lithology with minor granitic rocks (the acidic suite). Geochemical evolution of the complex in the sequence anorthosite-leuconorite-norite-jotunite-acidic rocks shows moderate iron enrichment in the noritic-jotunitic stage and is marked by an overall decrease in Al₂O₃, CaO, MgO, Ni/Co, Sr/Ba, K/Rb and increase in SiO₂, K₂O, V/Ni, K/Ba and Rb/Sr. Such progressive variation in geochemical parameters appears (i) essentially gradual and frequently overlapping in rock members of the intergradational anorthositic suite and (ii) rather abrupt across transition zones between the anorthositic suite and the acidic suite due to near absence of intervening intermediate lithologies. RbSr whole rock isochron studies indicate that the complex was emplaced ca. 1400 Ma ago. The initial ⁸⁷Sr/⁶⁸Sr (0.70661) implies limited hybridisation of the parent magma prior to emplacement. A critical appraisal of all the available evidence suggests that (i) the anorthositic suite of rocks form a perfectly consanguinous and comagmatic assemblage and (ii) the spatially associated acidic suite emerged through a convergence of magmatic and metasomatic processes (the latter brought about by contact anatexis of the host rocks). The complex as well as the host metamorphics are intruded by an atectonic suite of noritic dykes emplaced ca 850 Ma ago.     

Ree minerals of alkaline metasomatic rocks in the Main Sayan Fault

The composition of accessory REE minerals (allanite, chevkinite, fergusonite, and REE carbonates) in alkaline metasomatic rocks of the Main Sayan Fault (quartz-albite-microcline-riebeckite-aegirine, quartzalbite-microcline-magnetite, and clinopyroxene-albite) was studied using back-scattered scanning electron microscopy. Chevkinite occurs only in quartz-albite-microline metasomatic rock. The paragenesis of allanite and titanite is stable in clinopyroxene-albite metasomatic rocks. Allanite and fergusonite are typical of all zones of the metasomatic column. Chevkinite and allanite are often altered due to interaction with hydrothermal fluid and lose some amount of LREE. Secondary bastnaesite, synchysite, and ancylite are formed after allanite, while secondary monazite is developed after chevkinite. Presumably, the low-temperature alteration of allanite and chevkinite under effect of F^?, CO ₃ ^2? , and P ₄ ^3? -bearing fluids had not any significant manifestation in the total REE content in metasomatic rocks.     

安徽沙坪沟斑岩钼矿床赋矿岩体钾质交代作用及其微量元素和Sr-Nd同位素响应

以沙坪沟钼矿主要的赋矿岩石——石英正长岩和花岗斑岩为对象,通过对比不同蚀变强度岩石的岩相学、岩石地球化学和同位素特征,研究该矿床的钾质交代作用-矿化特征,探讨不同热液蚀变的元素组合、蚀变过程中的元素迁移和Sr-Nd同位素的变化及其成因、不同蚀变的物理化学条件差异及其与矿化的关系,进而揭示蚀变-成矿热液流体的特征和起源。研究表明,石英正长岩和花岗斑岩的地球化学特征总体相似,显示其属同源岩浆演化产物,二者均受到钾质蚀变,但蚀变强度相差较大。钾质蚀变岩石的化学成分表现为高K_2O、Rb和低Na_2O、CaO、Sr、Ba,不同蚀变强度的岩石Rb/Sr和Sr同位素组成差别较大,花岗斑岩样品数据更显离散,甚至出现异常低的锶同位素初始值,表明热液蚀变强烈改造了Rb-Sr同位素体系,而Sm-Nd体系基本保持稳定。这一现象在东秦岭-大别钼矿带中典型的斑岩钼矿床也有出现,显示该成矿带具有相似的蚀变类型、热液起源和演化特征。而且钾长石化后期至黄铁云(绢)英岩化阶段也是最主要的钼成矿期,表明这期间流体系统pH值的降低致使Mo元素从流体中沉淀成矿。对比斑岩铜、铜-钼矿床和钼矿床的蚀变特征及其过程中元素和同位素的变化可以发现,这3种矿床均发育碱质交代作用,但蚀变强度、热液的Rb-Sr分异程度及其对原岩的改造程度存在较大差异,这暗示了各自特有的成岩、成矿物质和流体来源及大地构造背景。