Age and geochemistry of the Newania dolomite carbonatites, India: implications for the source of primary carbonatite magma

The Newania carbonatite complex of India is one of the few dolomite-dominated carbonatites of the world. Intruding into Archean basement gneisses, the rocks of the complex have undergone limited diversification and are not associated with any alkaline silicate rock. Although the magmatic nature of the complex was generally accepted, its age of emplacement had remained equivocal because of the disturbed nature of radioisotope systems. Many questions about the nature of its mantle source and mode of origin had remained unanswered because of lack of geochemical and isotopic data. Here, we present results of our effort to date the complex using ¹⁴⁷Sm–¹⁴³Nd, ²⁰⁷Pb–²⁰⁶Pb and ⁴⁰Ar–³⁹Ar dating techniques. We also present mineral chemistry, major and trace element geochemistry and Sr–Nd isotopic ratio data for these carbonatites. Our age data reveal that the complex was emplaced at ~1,473 Ma and parts of it were affected by a thermal event at ~904 Ma. The older ²⁰⁷Pb–²⁰⁶Pb ages reported here (~2.4 Ga) and by one earlier study (~2.3 Ga; Schleicher et al. Chem Geol 140:261–273, 1997) are deemed to be a result of heterogeneous incorporation of crustal Pb during the post-emplacement thermal event. The thermal event had little effect on many magmatic signatures of these rocks, such as its dolomite–magnesite–ankerite–Cr-rich magnetite–magnesio-arfvedsonite–pyrochlore assemblage, mantle like δ¹³C and δ¹⁸O and typical carbonatitic trace element patterns. Newania carbonatites show fractional crystallization trend from high-Mg to high-Fe through high-Ca compositions. The least fractionated dolomite carbonatites of the complex possess very high Mg# (≥80) and have similar major element oxide contents as that of primary carbonatite melts experimentally produced from peridotitic sources. In addition, lower rare earth element (and higher Sr) contents than a typical calcio-carbonatite and mantle like Nb/Ta ratios indicate that the primary magma for the complex was a magnesio-carbonatite melt and that it was derived from a carbonate bearing mantle. The Sr–Nd isotopic data suggest that the primary magma originated from a metasomatized lithospheric mantle. Trace element modelling confirms such an inference and suggests that the source was a phlogopite bearing mantle, located within the garnet stability zone.     

印度南部元古代Cudappah盆地白云岩中的菱镁矿成矿作用及其构造-气候指示意义

Cudappah盆地是位于印度南部的一个元古代盆地,盆地中含有许多矿床,包括菱镁矿和滑石矿。该盆地发育于Chat活动带东部边缘,并发育沙质、粘土质和碳酸盐岩的多期重复沉积旋回。盆地可划分为四个次级盆地,即Papaghni、Nallamalai、Srisailam和Kurnool次级盆地。晶质菱镁矿床赋存于Papashni次级盆地的Vempalli组地层中。每个次级盆地很可能都沿着一系列裂谷中的断块发育,并且这些裂谷形成于中元古代的热事件。每个沉积旋回中发育有相似的沉积岩套表明,在盆地演化过程中具有相同的构造和气候环境。根据盆地中矿床(重晶石矿、菱镁矿和滑石矿)的产出,我们对每个次级盆地均提出了一个多期重复沉积旋回的演化模式,该旋回包括了从角砾岩到白云岩的变化。     

Mineral geochemistry of the Sangan skarn deposit,NE Iran: Implication for the evolution of hydrothermal fluid

The Sangan iron skarn deposit is located in the Sabzevar-Dorouneh Magmatic Belt of northeastern Iran. The skarn contains zoned garnet, clinopyroxene and magnetite. Cores and rims of zoned garnets are generally homogeneous, having a relatively high ΣREE, low ΣLREE/ΣHREE ratios, and positive Eu anomalies. The cores of the zoned clinopyroxenes are exceptionally HREE-rich, with relatively high ΣREE and HREE/LREE ratios, as well as positive Eu anomalies. Clinopyroxene rims are LREE-rich, with relatively low ΣREE contents and HREE/LREE ratios, and do not have Eu anomalies. Magnetite grains are enriched in LREEs in comparison with the HREEs and lack Eu anomalies. Variations of fluid composition and physicochemical conditions rather than YAG-type substitution mechanism are considered to have major control on incorporating trace elements, including REE, into the skarn mineral assemblage. Based on baro-acoustic decrepitation analysis, the calc-silicate and magnetite dominant stages were formed at similar temperatures, around 350–400 °C. In the Sangan skarns, hydrothermal fluids shifted from near-neutral pH, reduced conditions with relatively high ΣREE, low LREE/HREE ratios, and U-rich characteristics towards acidic, oxidized conditions with relatively low ΣREE, high LREE/HREE ratios, and U-poor characteristics.     

Grain growth kinetics of dolomite,magnesite and calcite: a comparative study

The rates of grain growth of stoichiometric dolomite [CaMg(CO₃)₂] and magnesite (MgCO₃) have been measured at temperatures T of 700–800°C at a confining pressure P _c of 300 MPa, and compared with growth rates of calcite (CaCO₃). Dry, fine-grained aggregates of the three carbonates were synthesized from high purity powders by hot isostatic pressing (HIP); initial mean grain sizes of HIP-synthesized carbonates were 1.4, 1.1, and 17 μm, respectively, for CaMg(CO₃)₂, MgCO₃, and CaCO₃, with porosities of 2, 28, and 0.04% by volume. Grain sizes of all carbonates coarsened during subsequent isostatic annealing, with mean values reaching 3.9, 5.1, and 27 μm for CaMg(CO₃)₂, MgCO₃, and CaCO₃, respectively, in 1 week. Grain growth of dolomite is much slower than the growth rates of magnesite or calcite; assuming normal grain growth and n = 3 for all three carbonates, the rate constant K for dolomite (≃5 × 10⁻⁵ μm³/s) at T = 800°C is less than that for magnesite by a factor of ~30 and less than that for calcite by three orders of magnitude. Variations in carbonate grain growth may be affected by differences in cation composition and densities of pores at grain boundaries that decrease grain boundary mobility. However, rates of coarsening correlate best with the extent of solid solution; K is the largest for calcite with extensive Mg substitution for Ca, while K is the smallest for dolomite with negligible solid solution. Secondary phases may nucleate at advancing dolomite grain boundaries, with implications for deformation processes, rheology, and reaction kinetics of carbonates.     

The crystallographic fabric and texture of siderite in concretions: implications for siderite nucleation and growth processes

The crystallographic fabric of siderite in siderite concretions has been determined for upper Carboniferous (Westphalian‐A) non‐marine concretions and lower Jurassic (Pliensbachian) marine concretions. Compositional zoning indicates that individual siderite crystals grew over a period of changing pore water chemistry, consistent with the concretions being initially a diffuse patch of cement, which grew progressively. The siderite crystallographic fabric was analysed using the anisotropy of magnetic susceptibility, which is carried by paramagnetic siderite. The siderite concretions from marine and non‐marine formations exhibit differences in fabric style, although both display increases in the degree of preferred siderite c‐axis orientation towards the concretion margins. The Westphalian non‐marine siderites show a preferred orientation of siderite c‐axes in the bedding plane, whereas the Pliensbachian marine siderites have a preferred orientation of c‐axes perpendicular to the bedding. In addition, a single marine concretion shows evidence of earlier formed, inclined girdle‐type fabrics, which are intergrown with later formed vertical c‐axis siderite fabrics. The marine and non‐marine fabrics are both apparently controlled by substrate processes at the site of nucleation, which was probably clay mineral surfaces. Siderite nucleation processes on the substrate were most probably controlled by the (bio?) chemistry of the pore waters, which altered the morphology and crystallographic orientation of the forming carbonate. The preferred crystallographic orientation of siderite results from the orientation of the nucleation substrate. Fabric changes across the concretions partially mimic the progressive compaction‐induced alignment of the clay substrates, while the concretion grew during burial.     

Petrology,geochemistry and geochronology of the Zhongcang ophiolite,northern Tibet: implications for the evolution of the Bangong-Nujiang Ocean

Ophiolites are widespread along the Bangong-Nujiang suture zone, northern Tibet. However, it is still debated on the formation ages and tectonic evolution process of these ophiolites. The Zhongcang ophiolite is a typical ophiolite in the western part of the Bangong-Nujiang suture zone. It is composed of serpentinized peridotite, cumulate and isotropic gabbros, massive and pillow basalts, basaltic volcanic breccia, and minor red chert. Zircon SHRIMP Ue Pb dating for the isotropic gabbro yielded weighted mean age of 163.4 ± 1.8 Ma. Positive zircon ε Hf(t) values(+15.0 to +20.2) and mantle-like σ~(18)O values(5.29 ±0.21)% indicate that the isotropic gabbros were derived from a long-term depleted mantle source. The isotropic gabbros have normal mid-ocean ridge basalt(N-MORB) like immobile element patterns with high Mg O, low TiO_2 and moderate rare earth element(REE) abundances, and negative Nb,Ti, Zr and Hf anomalies. Basalts show typical oceanic island basalt(OIB) geochemical features, and they are similar to those of OIB-type rocks of the Early Cretaceous Zhongcang oceanic plateau within the Bangong-Nujiang Ocean. Together with these data, we suggest that the Zhongcang ophiolite was probably formed by the subduction of the Bangong-Nujiang Ocean during the Middle Jurassic. The subduction of the Bangong-Nujiang Tethyan Ocean could begin in the Earlye Middle Jurassic and continue to the Early Cretaceous, and finally continental collision between the Lhasa and Qiangtang terranes at the west Bangong-Nujiang suture zone probably has taken place later than the Early Cretaceous(ca. 110 Ma).     

Carbon-oxygen isotopic geochemistry of the Yangla Cu skarn deposit,SW China: Implications for the source and evolution of hydrothermal fluids

The Yangla Cu deposit is the largest Cu skarn deposit in the Jinshajiang tectonic belt. Based on the detailed observation of crosscutting relationships, three mineralization stages (i.e., pre-ore, ore and supergene) have been identified in the Yangla deposit. The pre-ore stage is dominated by prograde skarn. The ore stage is characterized by the precipitation of hydrous silicate minerals, Fe-oxides, Fe-Cu-Mo-sulfides, quartz and calcite, whose mineral assemblages were formed in the early and late sub-ore stages. The early sub-ore stage is marked by retrograde alteration with the deposition of hydrous silicate minerals (e.g., actinolite, epidote and chlorite), Fe-oxides, abundant Fe-Cu-Mo-sulfides, quartz and minor calcite. Whilst, the late sub-ore stage, associated with silicic and carbonate alteration, is represented by widespread thick quartz or calcite veins with disseminated pyrite, chalcopyrite, galena and sphalerite. We present new carbon-oxygen (C-O) isotopic compositions of the ore-hosting marble and hydrothermal calcite of this deposit. The hydrothermal calcite in the Yangla deposit was precipitated from both the early and late sub-ore stages. Calcite I from the early sub-ore stage is anhedral, and occurs as spot in the skarn or locally replaces the skarn minerals. Calcite II from the late sub-ore stage is distinguished by being coarse-grained, subhedral to euhedral and its occurrence in thick veins. Calcite I contains lower δ¹³C_PDB (−7.0‰ to −5.0‰) and δ¹⁸O_SMOW (7.2‰ to 12.7‰) than Calcite II (δ¹³C_PDB = −4.5‰ to −2.3‰; δ¹⁸O_SMOW = 10.7‰ to 19.4‰). In the δ¹³C_PDB vs. δ¹⁸O_SMOW diagram, the Calcite I and Calcite II data fall close to the igneous carbonatite field and between the fields of igneous carbonatite and marine carbonates, respectively. This suggests a dominantly magmatic origin for the early sub-ore fluids, and there might have been increasing carbonate wall rock involvement towards the late sub-ore stage. The ore-hosting marble (δ¹³C_PDB = −4.8‰ to −0.3‰; δ¹⁸O_SMOW = 10.2‰ to 23.9‰) also shows a positive δ¹³C_PDB vs. δ¹⁸O_SMOW correlation, which is interpreted to reflect the decreasing alteration intensity during the interactions between the hydrothermal fluids and ore-hosting carbonates. Simulated calculation suggests that both the Calcite I and Calcite II precipitated at 350 °C to 250 °C and 250 °C to 150 °C, respectively. We proposed that CO₂ degassing and water/rock interactions were likely the two major processes that precipitated the calcite and led to the observed C-O isotopic features of the Yangla Cu deposit.     

A model for the distribution of trace elements between calcite and dolomite

A crystal-growth model is proposed, which allows ions of a trace element to enter the Ca and Mg sites of dolomite in proportion to the size of the ions relative to that of Ca and Mg ions, and which assigns equal portions of the trace element to the Ca site of dolomite and the Ca site of associated calcite. The model produces calcite/dolomite distribution coefficients of 0.79 for Mn and 0.43 for Fe, which may be compared with 0.85 and 0.28 as observed in marble, and a distribution coefficient of 2.0 for Sr and Ba, which may be compared with observed values of 2.3 for Sr and 1.8 for Ba.     

Ultramafic rocks of the Widgiemooltha-Norseman area,Western Australia: Petrological diversity,geochemistry and mineralisation

Mineral exploration of the Widgiemooltha-Norseman region of Western Australia has located massive and disseminated nickel sulphide mineralisation.This paper discusses the geological setting of the nickel sulphide mineralisation with reference to the stratigraphy, structure and metamorphism of the ultramafic sequence and spatially associated rocks. The amphibolite facies metamorphosed ultramafic rocks of the Widgiemooltha area are compared with greenschist metamorphosed ultramafic rocks at Eundynie, which exhibit excellently preserved pseudomorphs of primary igneous textures.Some 2000 ultramafic rock samples were analysed for 13 element/oxides and divided into four major mineralogically and texturally distinct groups. The data were analysed statistically by determination of means and standard deviations and multiple regression analyses.The data suggest differentiation of a magma at depth followed by a vast outpouring of lava to produce picritic-peridotitic rocks. The flows crystallised with upper spinifex zones and lower euhedral-olivine zones in varying proportions dependent on magma composition. The development of spinifex texture is compositionally controlled. This texture is not developed in rocks with MgO contents greater than 26% (± 2%).The comparison of the ultramafics of the Widgiemooltha and Eundynie areas indicates that talc-carbonate formation and serpentinization have modified primary igneous textures and geochemistries, resulting in the production of a diverse group of rock types. Such post-magmatic alteration processes in association with structural elements are considered important in the upgrading of nickel sulphide mineralisation.     

钾长石在碱性条件下的蚀变机制及其蚀变产物托贝莫来石的纳米结构研究

钾长石在碱性流体蚀变过程中会形成层状铝硅酸盐等矿物,前人对其反应机制和反应产物进行了研究,但缺乏微观尺度尤其是纳米尺度的探讨。因此,作者对钾长石在极端碱性条件下(190℃,24h,初始p H=12.4)的蚀变机制及其蚀变产物层状硅酸盐托贝莫来石的显微结构开展了纳米尺度的研究。X射线粉末衍射、扫描电子显微镜、能量色散光谱等观测结果显示,钾长石在碱性条件下水热蚀变所得到的产物主要为托贝莫来石、水钙铝榴石和方解石。高分辨率的透射电镜结果表明,在钾长石与次生矿物相的界面形成了纳米级的多孔非晶质层,且在空间上表现出结构的不连续性。界面溶解-再沉淀(CIDR)机制很好地解释了钾长石与次生矿物相界面的空间不连续性和非晶质层的形成。对蚀变产物中纤维状的托贝莫来石晶体进行显微结构表征,结果表明托贝莫来石的孔隙直径为0～160nm,平均孔径约为40nm;其构成的纳米孔隙和通道有利于增加周围流体中离子和气体的溶解度,并可能会影响局部化学平衡。这为层状铝硅酸盐作为自然界以及工业吸附材料和催化剂的更广泛应用提供了重要依据。     

Timing of orogenic gold mineralisation in northeastern Tasmania: implications for the tectonic and metallogenetic evolution of Palaeozoic SE Australia

New ⁴⁰Ar/³⁹Ar data from sedimentary rock-hosted orogenic gold deposits in northeastern Tasmania constrain most ore formation to between 395 Ma and 385 Ma. These 385–395 Ma ages for the formation of orogenic gold agree well with an inferred Early to Middle Devonian timing for peak deformation and folding across much of northeastern Tasmania. Data from micas within alteration halos in some deposits give dates of ~420–430 Ma; these dates confirm the occurrence of an earlier Silurian phase of deformation and suggest that at least some of the mineralisation was possibly generated during this event. Gold mineralisation hosted by Middle Devonian post-tectonic granites may be genetically related to magmatism following orogeny, but these deposits formed virtually synchronously with peak deformation-related systems. Early to Middle Devonian deformation in northeastern Tasmania also reactivated older structures in western Tasmania, and the formation of quartz vein-hosted gold mineralisation there. Based on geological, structural, tectonic and metallogenetic similarities, northeastern Tasmania is interpreted as a lateral equivalent of the turbidite-dominated fold-thrust belt of the western Lachlan Orogen. However, unlike Victoria, where the sedimentary rock sequence developed on oceanic crust, northeastern Tasmania was probably underlain by thinned Proterozoic crust, either as part of a promontory along the Gondwana margin or as a microcontinental fragment. This may have protected the Palaeozoic succession from large-scale, pre-Devonian orogeny, with collision not beginning until the Middle Devonian. These variations in the structural and tectonic evolution, and the timing of deformation and ore formation can explain the difference in contained gold, and the distribution and number of major orogenic gold deposits within the Palaeozoic of northeastern Tasmania.Electronic supplementary material Supplementary material is available for this article at     

Oxygen isotope geochemistry of the Omeo Metamorphic Complex,Victoria: Implications for metamorphic fluid flow,mineralisation and anatexis

Metamorphosed turbidites from the Omeo Metamorphic Complex show only minor changes in δ¹⁸O values with increasing metamorphic grade from 13.4 ± 1.7% in the chlorite and biotite zones to 12.3 ± 1.0% in the sillimanite + K‐feldspar zone. Rocks within 5 km of the S‐type granite at Hume Dam have δ¹⁸O values of 6.8–8.1% that probably reflect interaction with heated meteoric‐igneous fluids. Interaction with igneous fluids has also occurred close to other I‐ and S‐type granites in this region. However, pervasive metamorphic fluid‐rock interaction in this terrain did not occur, which limits the region's potential for hydrothermal mineralisation. Anatexis at high grades was probably via dehydration‐melting reactions that consumed muscovite and biotite, which is consistent with there being little fluid present during metamorphism. Small (kilometre scale or less) S‐type granites in the sillimanite + K‐feldspar zone have δ¹⁸O values similar to those of the surrounding metasediments and probably formed by melting of those rocks. By contrast, larger (tens of kilometres scale) Ca‐rich, peraluminous, S‐type granites have lower δ¹⁸O values than the surrounding metasediments, and may represent melts of underlying middle to lower crust.     

High-density nitrogen inclusions in barite from a giant siderite vein: implications for Alpine evolution of the Variscan basement of Western Carpathians, Slovakia

Contrasting compositions and densities of fluid inclusions were revealed in siderite–barite intergrowths of the Dro?diak polymetallic vein hosted in Variscan basement of the Gemeric unit (Central European Carpathians). Primary two‐phase aqueous inclusions in siderite homogenized between 101 and 165 °C, total salinity ranged between 18 and 27 wt%, and CaCl₂/(NaCl + CaCl₂) weight ratios were fixed at 0.1–0.3. By contrast, mono‐ and two‐phase aqueous inclusions in barite exhibited total salinities between 2 and 22 wt%, and the CaCl₂/NaCl ratios ranged from NaCl‐ to CaCl₂‐dominated compositions. The aqueous inclusions in barite were closely associated with very high‐density (0.55–0.745 g cm^?3) nitrogen inclusions, in some cases containing up to 16 mol.% CO₂. Crystallization P–T conditions of siderite (175–210 °C, 1.2–1.7 kbar) constrained by the vertical oxygen isotope gradient along the studied vein, isochores of fluid inclusions and the K/Na exchange thermometer corresponded to minimal palaeodepths between 4.3 and 6.3 km, assuming lithostatic load and average crust density of 2.75 g cm^?3. Maximum fluid pressure during barite crystallization attained 3.6–4.4 kbar at 200–300 °C, and the most dense nitrogen inclusions maintained without decrepitation the residual internal pressure of 2.2 kbar at 25 °C. Contrasting fluid compositions, increasing depths of burial (～4–14 km) and decreasing thermal gradients (～40–15 °C km^?1) during initial mineralization stages of the Dro?diak vein reflect Alpine orogenic processes, rather than an incipient Permian rifting suggested in previous metallogenetic models. Siderite crystallized at rising P–T in a closed, rock‐buffered hydrothermal system developed in the Variscan basement during the north‐vergent Cretaceous thrusting and thickening of the Gemeric crustal wedge. Variable salinities of the barite‐hosted inclusions reflect a fluid mixing in open hydrothermal system, and re‐equilibration textures (lengths of decrepitation cracks proportional to fluid inclusion sizes) correspond to retrograde crystallization trajectory coincidental with transpression or unroofing. Maximum recorded fluid pressures indicate ～12‐km‐thick pile of imbricated nappe units accumulated over the Gemeric basement during the Cretaceous collision.     

Oxygen isotope fractionation during synthesis of CaMg-carbonate and implications for sedimentary dolomite formation

Hydrous CaMg-carbonate was synthesized at temperatures of 40°, 60° and 80°C in the laboratory. This material has very similar mineralogical characteristics to natural disordered dolomite from the Coorong region in South Australia. Besides the dolomite variable amounts of amorphous carbonate are present in all samples. The oxygen isotope compositions of synthesized bulk carbonate samples (e.g., amorphous carbonate plus dolomite) plot significantly lower than the Northrop and Clayton (1966) dolomite-water equilibrium. Fractionated degassing of the samples, however, revealed relatively low oxygen isotope values for fast-reacting (using 100% H₃PO₄) amorphous carbonate. In contrast, slow-reacting dolomite has more positive oxygen isotope values, and calculated carbonate-water oxygen isotope fractionation values are close to strongest known dolomite-water oxygen isotope fractionation published earlier on. Variations of reaction/stabilization temperatures during synthesis gave evidence for dolomite formation from hypersaline solutions by a dissolution/reprecipitation process. It is likely that amorphous carbonate has been a problem in defining the dolomite-water fractionation in the past. Moreover, dolomite-associated amorphous carbonate contents probably led to incorrect speculations about lower oxygen isotope fractionation in a so-called protodolomite-water system.     

REE systematics of fluorides,calcite and siderite in peralkaline plutonic rocks from the Gardar Province,South Greenland

The Gardar failed-rift Province is world-famous for its (per-)alkaline plutonic rocks. Elevated contents of F in the mantle source and F-enrichment in the parental melts have been suggested to account for the peculiarities of the Gardar rocks (e.g. their rare mineralogy, extreme enrichment of HFSE elements, Be or REE in the Ilímaussaq agpaites, and the formation of the unique Ivigtut cryolite deposit). To constrain the formation and chemical evolution of F-bearing melts and fluids, fluorides (fluorite, cryolite, villiaumite, cryolithionite), calcite and siderite from the Ilímaussaq, Motzfeldt and Ivigtut complexes were analysed for their trace element content focusing on the rare earth elements and yttrium (REE).The various generations of fluorite occurring in the granitic Ivigtut, agpaitic Ilímaussaq and miaskitic to agpaitic Motzfeldt intrusions all share a negative Eu anomaly which is attributed to (earlier) feldspar fractionation in the parental alkali basaltic melts. This interpretation is supported by the abundance of anorthositic xenoliths in many Gardar plutonic rocks.The primary magmatic fluorites from Ilímaussaq and Motzfeldt display very similar REE patterns suggesting a formation from closely related parental melts under similar conditions. Hydrothermal fluorites from these intrusions were used to constrain the multiple effects responsible for the incorporation of trace elements into fluorides: temperature dependence, fluid migration/interaction and complexation resulting in REE fractionation. Generally, the REE patterns of Gardar fluorides reflect the evolution and migration of a F/CO₂-rich fluid leading to the formation of fluorite and fluorite/calcite veins. In certain units, this fluid inherited the REE patterns of altered host rocks. In addition, there is evidence of an even younger fluid of high REE abundance which resulted in highly variable REE concentrations (up to three orders of magnitude) within one sample of hydrothermal fluorite.The REE patterns of the granitic Ivigtut intrusion show flat to slightly heavy-REE-enriched patterns characterised by a strong tetrad effect. This effect is interpreted to record extensive fluid–rock interaction in highly fractionated, Si-rich systems.Interestingly, the fluorides appear to record different source REE patterns, as the spatially close Motzfeldt and Ilímaussaq intrusions show strong similarities and contrast with the Ivigtut intrusion located 100 km NE. These variations may be attributed to differences in the tectonic position of the intrusions or mantle heterogeneities.     

Mineralogical and geochemical characteristics of hydrothermal alteration of basalt in the Kuroko mine area, Japan: implications for the evolution of a Back Arc Basin hydrothermal system

Basalt in the Furutobe District of the Kuroko mine area in Japan is characterized by abundant chlorite and epidote. Fluid inclusion studies indicate that chlorite is formed at lower temperatures (230–250°C) than epidote (250–280°C). The seawater/basalt mass ratio for the early chlorite-rich alteration was high (max. 40), but that for the later alteration was low (0.1–1.8). The CaO, Na₂O and SiO₂ of the bulk rock correlate negatively with MgO, while FeO and Σ Fe correlate positively with MgO. These changes in the characteristic features of hydrothermal alteration from early to late are generally similar to those for a mid-ocean ridge geothermal system accompanying basalt alteration.The MgO/FeO ratios of chlorite and actinolite and the Fe₂O₃ concentration of epidote from the basalt are greater than those of mid-ocean ridge basalt probably owing to the differences in the Fe₂O₃/FeO and MgO/FeO ratios of the parent rocks. The lower CaO concentration and the higher Na₂O concentration of the bulk rock compared with altered mid-ocean ridge basalt can be interpreted in terms of the difference in original bulk rock compositions.The Furutobe basalt, as well as other submarine back arc basalts, contains more vesicles filled with hydrothermal minerals (epidote, calcite, quartz, chlorite, pyrite) than do the mid-ocean ridge basalts. The abundance of vesicles plays an important role in controlling the secondary mineralogy and geochemistry of hydrothermally altered submarine back arc basin basalts.     

Implications of pyrite geochemistry for gold mineralisation and remobilisation in the Jiaodong gold district,northeast China

The Jiaodong gold district of eastern China, the largest gold producing district in China, is located on the eastern margin of the North China Craton. It consists of three mineralisation belts: the western Zhao-Ye belt, the middle Qixia belt, and the eastern Muping–Rushan (Muru) belt. Over 85% of mineralisation is hosted in the Zhao-Ye belt, which is bordered by the mantle-tapping Tan Lu fault zone. Pyrite crystals from three deposits in the Zhao-Ye belt and three deposits in the Muru belt were studied using a combination of optical petrography, bulk pyrite geochemistry, and in-situ laser ablation ICP-MS. Results show that although mineralisation is broadly similar between the two belts, there are significant differences in ore and gangue mineral textures, pyrite geochemistry, and style of gold mineralisation.Texturally, pyrite grains from the Zhao-Ye belt are generally cubic and do not exhibit zoning. In contrast, Muru pyrite grains are more often pyritohedral, commonly exhibit well-defined concentric zoning, and display textures in ore and gangue minerals indicative of open space growth. Bulk pyrite geochemistry suggests a distinct enrichment in Pb, Bi, Au, Ag and Te in the Zhao-Ye belt, whereas the Muru belt pyrite is significantly enriched in As, Cu and Co. In situ pyrite geochemistry indicates that Au and As are variably correlated in the Zhao-Ye belt, typically only exhibiting correlation at low Au concentrations. Most gold occurs as visible electrum along pyrite fractures and grain boundaries, with a minor generation of invisible gold formed through As-facilitated uptake into pyrite. In the Muru belt, Au and As have a strong correlation and there is limited occurrence of gold particles, indicating that most gold in the Muru belt is invisible gold contained in the crystal structure of As-rich pyrite.The differences in style of gold mineralisation between the belts indicates an inherent difference in timing of gold introduction: in the Zhao-Ye belt, the visible electrum accounting for most of the gold endowment is formed post-pyrite, whereas the invisible gold in the Zhao-Ye and Muru belts is formed syn-pyrite. The heterogeneity in gold distribution in the Jiaodong district is attributed to melting of metallogenically fertile Archean crust at the base of the well-endowed Zhao-Ye belt, and the lack of a similarly fertile source region beneath the Muru belt.     

白钨矿地球化学对皖南竹溪岭和逍遥钨矿成矿流体演化的指示

近年来赣北-皖南地区陆续发现了一批斑岩-矽卡岩钨矿床,构成一个新的世界级钨成矿带——江南钨矿带。位于该成矿带东北段的皖南地区发育大量与弱分异氧化性花岗岩相关的钨多金属矿床,目前这类矿床缺乏基于矿物原位地球化学的精细研究,成矿流体性质和演化认识不清。本文选取皖南地区两个代表性钨多金属矿床——竹溪岭和逍遥矿床为研究对象,开展白钨矿原位成分分析,揭示矽卡岩体系成矿流体性质、物化条件变化以及水岩反应影响,并探讨江南钨矿带内钨成矿条件差异。白钨矿原位成分分析能够精细厘定矽卡岩形成过程的氧逸度、pH值、温度、成矿流体组成变化以及水岩反应等信息。逍遥矿床和竹溪岭矿床的白钨矿均可分为三个阶段：其中早期进变质矽卡岩中白钨矿(Sch-1)的Mo含量最高,REE表现为轻重稀土分异的右倾曲线,具有负Eu异常,与成矿母岩REE配分类似,指示早期流体是相对富Cl的岩浆出溶热液;Sch-2产于退变质矽卡岩阶段,其轻重稀土分异变弱,有一定的正Eu异常,REE和Mo含量较低,推测早期Sch-1结晶摄取大量的LREE,导致后期流体轻重稀土比值降低;脉状产出的白钨矿(Sch-3)形成于晚期石英-硫化物阶段,其REE、Nb、Ta和Y等元素含量显著高于Sch-1和Sch-2,REE表现为轻重稀土分异弱的平坦型曲线,发育弱正Eu异常,暗示晚期流体更加富F。本文研究认为从早期Sch-1到晚期Sch-3,白钨矿Eu异常变化不一定反映氧逸度变化,而更可能反映的是水岩反应制约;此外,白钨矿的Mo含量相对于Eu异常更能够有效地反映体系的氧逸度特征。与逍遥矿床相比,竹溪岭矿床石榴石的钙铁榴石组分含量较低,锰铝榴石组分含量高,白钨矿Mo含量(630×10^-6~18813×10^-6)显著低于逍遥白钨矿(8700×10^-6~74478×10^-6),指示竹溪岭矿床相比于逍遥矿床是相对还原的钨矽卡岩体系。前人认为江南钨矿带中相对于赣北还原型钨矽卡岩矿床,皖南地区矿床总体上属于氧化型,基于竹溪岭矿床和逍遥矿床的对比表明皖南地区钨矿床之间氧化还原状态存在差异。氧逸度和成矿岩浆岩的分异程度是制约皖南地区矿床规模大小的重要因素。

     

The Marl Slate: a model for the precipitation of calcite, dolomite and sulphides in a newly formed anoxic sea

Detailed studies of a new, complete Marl Slate core in South Yorkshire have provided information on isotopic (δ¹³C, δ¹⁸O, δ³⁴S) and geochemical variations (trace elements and C/S ratio) which enable the formulation of a model for carbonate and sulphide precipitation in the Late Permian Zechstein Sea. Calcite and dolomite are intimately associated; the fine lamination, organic character and absence of benthos in the sediments are indicative of anoxic conditions. Lithologically the core can be divided into a lower, predominantly sapropelic Marl Slate (2 m) and an upper Transition Zone (0·65 m) of alternating sapropel and calcite-rich and dolomite-rich carbonates. C/S ratios are 2·22 for the Marl Slate and 1·72 for the Transition Zone respectively, both characteristic of anoxic environments. δ¹⁸O in the carbonates shows a large and systematic variation closely mirrored by variations in calcite/dolomite ratio. The results suggest a fractionation factor equivalent to a depletion of 3·8% for ¹⁸O and 1·5% for ¹³C in calcite. The δ³⁴S values of pyrite are isotopically light (mean value = - 32·7%) suggesting a fractionation factor for the Marl Slate of almost 44%, typical of anoxic basins. The results are related to stratification in the early Zechstein Sea. Calcite was precipitated in oxic upper layers above the halocline. Below the oxic/anoxic boundary framboidal pyrite was precipitated, resulting in lower sulphate concentration and elevated Mg/Ca ratio (due to calcite precipitation). As a result of this, dolomite formation occurred below the oxic/anoxic interface, within the anoxic water column and in bottom sediments. Variations in calcite/dolomite ratios, and isotopic variations, are thus explained by fluctuations in the relative level of the oxic/anoxic boundary in the Zechstein Sea.