Fayalite from Fe-rich paralavas of ancient coal fires in the Kuzbass,Russia

Fayalite is a common mineral of Fe-rich paralavas related to spontaneous combustion of coal seams. Fayalite has also been found in parabasalts from burned coal waste piles of the Chelyabinsk coal basin. Among paralavas from different combustion metamorphic (CM) complexes of the world, fayalite is the most widespread in the fused rocks of the Kuznetsk coal basin (Kuzbass) and the Ravat area in Tajikistan. The optimal conditions for fayalite formation as products of coal fires in the Kuzbass and Ravat resulted from a favorable combination of the composition of fused protolith (parental rocks) composed of pelitic and Fe-rich sediments and the redox conditions of the deep subsurface ($ f_{O_2 } $ f_{O_2 } is lower than the QFM buffer). In the Kuzbass, fayalite is commonly hosted in high-silica aluminous Fe-rich paralavas composed of Fe-cordierite (sekaninaite), tridymite, hercynite-magnetite, cristobalite, aluminous clinoferrosilite, and Al-K silicic glass. The composition of all Kuzbass fayalites is close to the Fe₂SiO₄ end member. Kuzbass fayalites are characterized by a negligibly low CaO content and higher MnO and P₂O₅ contents like fayalites from burned rocks of other CM complexes. In Kuzbass paralavas, Fe-olivine is the late phase that crystallized after sekaninaite and tridymite, immediately before melt quenching.     

Monazite as an indicator of formation conditions of quartz veins at the Zhelannoe deposit,the Subpolar Urals

At the Zhelannoe quartz deposit, the content of monazite attains 0.5 wt % in unaltered sericitolite and 18 wt % in hydrothermally altered sericitolite. Two monazite generations, including four varieties, characterize the sequence of formation and alteration of sericitolite bodies at the Zhelannoe deposit. Monazite of the first generation occurs in unaltered sericitolite as prismatic and tabular crystals characterized by (Nd,Ce) > La and enrichment in HREEs and ThO₂ (5–16 wt %). Its formation is accompanied crystallization of milk white quartz. Monazite of the second generation occurs in altered sericitolite as the product of recrystallization of the first-generation monazite. The large drusy crystals of second-generation monazite were formed similarly with Alpine-type veins. Monazite of the second generation is characterized by Ce > (La,Nd), low contents of HREEs and ThO₂ (0.5–7 wt %) and high contents of CaO and SO₃ (up to 3–5 wt %). Monazite of the second generation appeared as a result of local superimposed processes and is a characteristic feature of the Zhelannoe deposit.     

Nature and origin of the protolith succession to the Paleoproterozoic Serra do Navio manganese deposit,Amapa Province,Brazil

Until its closure in 1997, the Serra do Navio deposit, located in Amapá Province, Brazil, was one of the most important sources of high-grade manganese ore to the North American market. The high-grade manganese oxide ores were derived by lateritic weathering from metasedimentary manganese protoliths of the Serra do Navio Formation. The local geological context and nature of this protolith succession are not well understood, due to poor surface outcrop conditions, and intense deformation. However, based on similar age, regional tectonic setting and lithology the Paleoproterozoic volcanosedimentary succession that includes the Serra do Navio Formation is widely believed to be similar in origin and laterally equivalent to the Birimian Supergroup in West Africa. For the present investigation several diamond drill cores intersecting the protolith succession were studied. Detailed petrographic and whole rock geochemical studies permit distinction of two fundamental lithological groups comprising of a total of five lithotypes. Biotite schist and graphitic schist lithotypes are interpreted as former metapelites. A greywacke or pyroclastic protolith cannot be excluded for the biotite schist, whereas the graphitic schist certainly originated as a sulfide-rich carbonaceous mudstone. Rhodochrosite marble, Mn-calcite marble and Mn-silicate rock are grouped together as manganiferous carbonate rocks. Manganese lutite constitutes the most probable protolith for rhodochrosite marble, whereas Mn-calcite marble was derived from Mn-rich marl and Mn-silicate rock from variable mixtures of Mn-rich marl and chert.The sedimentary succession at the Serra do Navio deposit is similar to that encountered at many other black shale and chert-hosted Mn carbonate deposits. A metallogenetic model is proposed, predicting deposition of manganese and closely associated chert in intra-arc basins, in environments that were bypassed by distal siliciclastic (carbonaceous mud) and proximal pyroclastic/siliciclastic detritus. Positive Ce anomalies and δ¹³C_VPDB values of − 4.3 to − 9.4 per mill suggest that manganiferous carbonates derived during suboxic diagenesis from sedimentary Mn⁴⁺ oxyhydroxide precipitates. Metamorphic alteration of manganese carbonate–chert assemblages resulted in the formation of Mn-silicates, most importantly rhodonite and tephroite; porphyroblastic spessartine formed where Mn-carbonate reacted with aluminous clay minerals. Microthermometric studies of fluid inclusions in spessartine porphyroblasts suggests that peak metamorphic conditions reached the upper greenschist facies (1–2 kbars and 400–500 °C). Retrograde metamorphism is marked by partial re-carbonation, expressed by the formation of small volumes of rhodochrosite, and Mn-calcite that are closely associated with quartz, chlorite and minor amounts of sulfides related to post-metamorphic veinlets. It is this metamorphosed succession that sourced the high-grade manganese oxide ores during prolonged lateritic weathering.     

Petrogenesis of Na-rich paralava formed by methane flares associated with mud volcanism, Altyn-Emel National Park, Kazakhstan

High-Na slag-like rocks (paralava) with 4.5–11 % Na₂O from the Altyn-Emel mud volcanic field, Kazakhstan, are the products of melting of sediment + salt mixtures by methane flares associated with mud extrusion. The main minerals of the paralavas are diopside and wollastonite which have quench morphologies. Other high-temperature phases (crystallizing from melt and vapour phase) are tridymite, cristobalite, chlorapatite, alkali feldspar, pyrrhotite, native iron and silicon, iron phosphides, titanite, rutile, and carbon. The paralavas lack the Na–Ca silicates devitrite and combeite, but have high-Na and Na–K glasses that have not been homogenized despite low viscosities of <10^?3.5 Pa s. The large number of ignition foci in the Altyn-Emel mud volcano field indicates gas venting from small, shallow reservoirs. The methane flares are inferred to have been small and the fire events short-lived. Fires were extinguished once overpressure released during eruption, methane venting stopped and melted rocks rapidly quenched. The periodicity of eruptions and methane flaring most likely depends on the recurrence of earthquakes (M < 5) which are frequent in this tectonically active area.     

U–Pb Dating of Hydrothermal Zircons from the Neoproterozoic Liushanyan VMS Cu–Zn Deposit,Central China: Evidence for a Triassic Deformation Event

The Liushanyan deposit is an important volcanic‐host massive sulfide (VMS) Cu–Zn deposit in the Qinling‐Tongbai‐Dabie orogenic belt, central China, with reserve of 2.38 Mt Cu and 16.11 Mt Zn. Orebodies occur in the meta‐quartz keratophyre of the Liushanyan formation. In this paper, we present textural features and laser ablation ICP‐MS U–Pb dating results of zircons from the ore‐bearing mylonitized meta‐quartz keratophyre. The hydrothermal zircons are distinct from metamorphic zircons in this rock, showing low cathodoluminescence (CL) response and hydrothermal rims (black in CL images). They have relatively flat light rare earth element patterns and high La content and low (Sm/La)_N and Ce/Ce* values. These features are typical of hydrothermal zircons. The cores of metamorphic zircons yield a weighted mean ²⁰⁶Pb/²³⁸U age of 900 ± 26 Ma, interpreted as the volcanic and related VMS mineralizing age. Two much younger events are also recorded by zircons in this rock: (i) the Early Silurian amphibolites–greenschist facies metamorphism at 435 ± 26 Ma; and (ii) the growth of hydrothermal zircons at ca. 241 ± 1 Ma, associated with the ductile shear deformation. The Silurian metamorphic event is probably associated with the arc–continent collision, while the Triassic ductile deformation event formed in the final continent–continent collision setting.     

中亚造山带中的燃烧变质事件及其年代学研究

Combustion metamorphic(pyrometamorphic)complexes produced by prehistoric natural coal fires are widespread inCentral Asia,namely at the interfaces between mountain systems and the flanking sedimentary basins.Large-scale and prolonged firesaccompanied the initial orogenic stages as unweathered coal-bearing formations became exposed into the aeration zone.Pyrometamorphic rocks are comparable to sanidinite facies rocks in formation conditions and in alteration of sedimentary material but,unlike these,their protolith underwent different melting degrees to produce either ferrous basic paralavas or glazed clinkers.The phasecomposition of the newly-formed melted rocks are favorable for~(40)Ar/~(39)Ar dating of combustion metamorphic events which are coeval tothe onset of the main stage of recent orogenic events.We suggest a new algorithm providing correct ~(40)Ar/~(39)Ar dating ofpyrometamorphic rocks followed by well-grounded geological interpretation.We studied pyrometamorphic rocks in the western Salairzone of the Kuznetsk coal basin where combustion metamorphism under temperatures above 1000℃acted upon large volumes of coal-bearing sediments.Samples of paralavas were dated by the step heating ~(40)Ar/~(39)Ar method checked against internal(plateau andisochrone ages)and external("criterions of couple")mineralogical criterions,and against preliminary dating from geological andstratigraphic evidence.As a result,we distinguished two groups of dates for combustion metamorphic events.The first one(1.2±0.4Ma)is drawn towards the west boundary of Prokopyevsk-Kiselevsk block of Salair zone,while the second one(0.2±0.3Ma)isconfined to its east boundary.The former ages represent rocks in the western edge of the Prokopievsk-Kiselevsk block of the Salair zoneand the latter ages correspond to those in its eastern edge.The dates record the time when the fault boundaries of the blocks wererejuvenated during recent activity and the block accreted to the Salair orogenic area as a piedmont step.These are the first absolute agesobtained for the onset of uplift of the northern edge of the Ahai-Sayan area,the key event of its neotectonic history.The suggestedapproach to the choice of objects,classification of rocks,and interpretation of~(40)Ar/~(39)Ar data is universal and can be practiced in anyarea subjected to combustion metamorphism.     

Zircon–quartz–calcite segregations in carbonate–alkaline metasomatic rocks of the western Baikal region and their petrogenetic implications

Fine-grained segregations up to 5 mm in size composed of graphic intergrowths of zircon, quartz, calcite and containing up to 0.8 wt % SrO have been found in albite–riebeckite and dolomite–biotite metasomatic rocks formed after alaskite granite. They contain magnetite, titanomagnetite (25.4 wt % TiO₂), cerite-(Ce,Nd), rutile (up to 1.2 wt % Nb₂O₅), as well as rare micrograins of monazite-(Ce), bastnaesite-(Ce), and barite (up to 5.7 wt % SrO). The fine-grained structure of mineral aggregates suggests a metacolloidal nature. It is assumed that the zircon–quartz–calcite assemblage was formed due to exchange decomposition reaction between the salt phase of hydrothermal solution with predominant Na₂CO₃, elevated Zr and, to a lesser extent, Fe, Ti, LREE, Nb contents and dissolved calcium and silica compounds of a Na₂SiO₃ type.     

Implications of geochemistry in support of Palaeo-Proterozoic tectonothermal evolution of bhopalpatnam Granulite Belt, Bastar Craton, Central India

Bhopalpatnam Granulite Belt which occur along SW margin of Bastar Craton and NE shoulder of Pranhita-Godavari Rift comprise of charnockite (enderbitic variety), garnet-sillimanite-biotite gneiss, quartzo-feldspathic gneiss and corundum bearing aluminous gneiss. High La/Yb ratio, low Eu anomaly (Eu/Eu*=1.0), high LREE/HREE ratio with uniform REE pattern, high La/Sc ratio (0.53–6.43), high Th/Sc ratio (0.03–2.56), low Ni (5.52–20.95), low Cr (31.05–117.05) and uniform Zr/Hf distribution pattern indicate a Proterozoic character. Distribution pattern of K₂O, Na₂O and CaO in ternary diagram show quartz-monzonite-granodiorite trend for the bulk rocks indicating that the bulk rock composition is close to TTG of early Archaean, which might have supplied the sediments for the rocks of Bhopalpatnam Granulite Belt. Geochemical and mineralogical evidence indicate an argillaceous protolith for garnet — sillimanite — biotite gneiss and corundum bearing aluminous gneiss, whereas an arkosic protolith for quartzo-feldspathic gneiss. The geochemical signatures also suggest an active continental margin setting for the rocks of Bhopalpatnam Granulite Belt with prominent Nb and Ta anomaly favouring a subduction environment between Bastar Craton and East Dharwar Craton. This is in conformity with the finding of the earlier workers suggesting a clockwise P-T path based on the combined fluid inclusion and mineral phase equilibria. The LILE geochemistry of charnockite suggests a bi-phase evolution. High LREE/HREE ratio portrays a highly evolved nature of the charnockitic melt generated through partial melting of the continental crust at the final stage of the granulite facies metamorphism during collision between Bastar and East Dharwar Cratons.     

Unique Clinkers and Paralavas from a New Nyalga Combustion Metamorphic Complex in Central Mongolia: Mineralogy,Geochemistry, and Genesis

The paper presents mineralogical and geochemical data on clinkers and paralavas and on conditions under which they were formed at the Nyalga combustion metamorphic complex, which was recently discovered in Central Mongolia. Mineral and phase assemblages of the CM rocks do not have analogues in the world. The clinkers contain pyrogenically modified mudstone relics, acid silicate glass, partly molten quartz and feldspar grains, and newly formed indialite microlites (phenocrysts) with a ferroindialite marginal zone. In the paralava melts, spinel microlites with broadly varying Fe concentrations and anorthite–bytownite were the first to crystallize, and were followed by phenocrysts of Al-clinopyroxene ± melilite and Mg–Fe olivine. The next minerals to crystallize were Ca-fayalite, kirschsteinite, pyrrhotite, minerals of the rhönite–kuratite series, K–Ba feldspars (celsian, hyalophane, and Ba-orthoclase, Fe³⁺-hercynite ± (native iron, wüstite, Al-magnetite, and fresnoite), nepheline ± (kalsilite), and later calcite, siderite, barite, celestine, and gypsum. The paralavas contain rare minerals of the rhönite–kuratite series, a new end-member of the rhönite subgroup Ca₄Fe ₈ ²⁺ Fe ₄ ³⁺ O₄ [Si₈Al₄O₃₆], a tobermorite-like mineral Ca₅Si₅(Al,Fe)(OH)O₁₆ · 5H₂O, and high- Ba F-rich mica (K,Ba)(Mg,Fe)₃(Al,Si)₄O₁₀F₂. The paralavas host quenched relics of microemulsions of immiscible residual silicate melts with broadly varying Si, Al, Fe, Ca, K, Ba, and Sr concentrations, sulfide and calcitic melts, and water-rich silicate–iron ± (Mn) fluid media. The clinkers were formed less than 2 Ma ago in various parts of the Choir–Nyalga basin by melting Early Cretaceous mudstones with bulk composition varies from dacitic to andesitic. The pyrogenic transformations of the mudstones were nearly isochemical, except only for volatile components. The CM melt rocks of basaltic andesitic composition were formed via melting carbonate–silicate sediments at temperatures above 1450°C. The Ca- and Fe-enriched and silicaundersaturated paralavas crystallized near the surface at temperatures higher than 900–1100°C and oxygen fugacity \(f_{O_2 }\) between the IW and QFM buffers. In local melting domains of the carbonate–silicate sedimentary rocks and in isolations of the residual melts among the paralava matrix the fluid pressure was higher than the atmospheric one. The bulk composition, mineral and phase assemblages of CM rocks of the Nyalga complex are very diverse (dacitic, andesitic, basaltic andesitic, basaltic, and silica-undersaturated mafic) because the melts crystallized under unequilibrated conditions and were derived by the complete or partial melting of clayey and carbonate–silicate sediments during natural coal fires.     

北大别大山坑二长花岗片麻岩的地球化学特征与锆石 U-Pb年代学

北大别东部大山坑片麻岩主要由钾长石、斜长石和石英组成,少量角闪石、黑云母和褐帘石,成分为二长花岗质。岩石以富碱（Na₂O＋K₂O）尤其是 K₂O、贫Al₂O₃为特征,地球化学性质上表现为富集 K、Rb、Th、La、Ce等大离子亲石元素而亏损Nb、Ta、U等高场强元素及Sr元素,高的Ga含量、强的负Eu异常（δEu＝0．37）和相对较强的轻重稀土分馏程度（（La／Yb）_N＝16．75）。岩石地球化学的总体特征与南大别水吼地区的 A型花岗片麻岩类似,意味着其原岩与南大别的 A型花岗片麻岩一样,可能也是在拉张状态下形成的一套偏碱性的花岗岩。该二长花岗片麻岩的锆石 U-Pb年龄为229．2±5．5 Ma,也与南大别超高压变质的年龄相似,指示北大别正片麻岩印支期可能也经历过超高压变质作用。南、北大别造山带可能具有相同的形成与演化历史,现南、北大别变质带之间的差异可能更多的是后造山历史不同,尤其是燕山期花岗岩侵入对两个带影响的不同造成的。     

Three Types of Apatite in Norilsk Sulfide Ores

Apatite is a concentrator of F and Cl, which play a significant role in the formation of minerals of platinum-group elements of pneumatolitic origin. There are three apatite generations in Norilsk magmatic sulfide ores. Apatite I occurs in sulfide bodies and rims of fluid alteration above sulfide droplets in disseminated ores. Its composition evolved from hydroxyl-chlorapatite to chlorapatite. Apatite I associates with Tiрbiotite, titanomagnetite, ilmenite with baddeleyite lamellae, anhydrite, Ti-poor kaersutite, Cl-bearing hastingsite and edenite, djerfisherite, bartonite, and minerals of the Pt and Au groups. Apatite I contains up to 2.3 wt % lanthanides, primarily Ce, La, and Nd. Apatite I is overgrown and replaced by apatite II, the composition of which evolved from hydroxyl-chlor-fluorapatite to fluorapatite. Apatite II often occurs also as individual crystals in massive sulfides and contains up to 0.9 wt % lanthanides. The pneumatolitic chlorapatite and fluorapatite contain ~0.5 wt % SiO₂. The composition of apatite indicates discrete evolution of fluids released during the crystallization of Norilsk sulfide melts: from water–chloride to chloride at the first state, and from water–chlorite–fluoride to essentially fluoride at the second stage. The lanthanides released during the replacement of chlorapatite I by fluorapatite II were probably incorporated in pneumatolitic zoned orthite-(Ce). In the areas affected by prehnite–pumpellyite metamorphism, apatite I and apatite II within metamorphosed sulfide ores are partly or completely replaced by apatite III, which varies in composition from hydroxyl-chlorapatite to hydroxylapatite poor in fluorine and lanthanides. The lanthanides released during the replacement of apatite I and II by metamorphic hydroxylapatite III were probably incorporated in metamorphic unzoned orthite-(Ce).     

Implications of elemental concentrations for provenance, redox conditions, and metamorphic studies of shales and limestones near Pueblo, CO, USA

Major element and some trace element compositions (including the REE) of shales, carbonate-rich shales, and limestones of Late Cretaceous age have been analyzed at two outcrops near Pueblo, CO. Elemental ratios that are characteristic of the provenance of terrigenous debris that are the least variable with changing percent acid insoluble residue vs. percent calcite are Th/Cr, La/Co, (La/Lu)_cn, and Eu/Eu*. The Ce/Ce*, La/Sc, and La/Cr ratios, however, are only constant when greater than 30% of a sample is composed of acid insoluble residue. At less than 30% acid insoluble residue, these elemental ratios increase markedly. The Th/Co and Th/Sc ratios are fairly constant from nearly 0% to about 60% acid-insoluble residue. Above 60% residue, these ratios increase due to the high concentration of Th in the Graneros to Hartland shales at Everhart Ranch. The average of the Th/Co, Th/Sc, Th/Cr, La/Co, La/Sc, and La/Cr ratios are similar to those of the MCS (mid-continent shales) and PAAS (Post-Archean Australian shales). Thus, these carbonate-rich to carbonate poor rocks analyzed in this study contain terrigenous debris that has been derived from granitoids similar to those that supplied debris to the MCS and PAAS. The Ce/Ce* ratios are lower and the Mn* (Mn*=log[(Mn_sample/Mn_shales)/(Fe_sample/Fe_shales)]) values are more positive in the more calcite-rich Bridge Creek and Ft. Hays limestones than in the other units, suggesting that they formed in an oxidizing environment. The Ce/Ce* are the highest and the Mn* values are the most negative in the Graneros to Hartland shales, suggesting that they formed under more reducing conditions.The elemental concentration of one sample relative to that of another sample over a few meters distance usually vary in small amounts (e.g., medians of the ratios of the same elements between adjacent samples ranges from 1.06 to 1.70). However, the ratio of elemental concentrations between adjacent samples can sometimes be quite large. The least variation of elemental ratios between adjacent samples often occurs within the more carbonate-poor shales; the greatest variation occurs within the limestones. Thus, trying to decipher local movement of elements due to metamorphism in similar carbonate shale-limestone sequences should be done cautiously since local elemental variation due to sedimentary processes can be large.     

Growth of myrmekite coronas by contact metamorphism of granitic mylonites in the aureole of Cima di Vila, Eastern Alps, Italy

In the contact aureole of the Oligocene granodiorite of Cima di Vila, granitic pegmatites of Variscan age were strongly deformed during eo‐Alpine regional metamorphism, with local development of ultramylonites. In the ultramylonite matrix, consisting of quartz, plagioclase, muscovite and biotite, microstructures show grain growth of quartz within quartz ribbons, and development of decussate arrangements of mica. These features indicate that dynamic recrystallization related to mylonite development was followed by extensive static growth during contact metamorphism. K‐feldspar porphyroclasts up to 1.5 cm are mantled by myrmekite that forms a continuous corona with thickness of about 1 mm. In both XZ and YZ sections, myrmekite tubules are undeformed, and symmetrically distributed in the corona, and oligoclase‐andesine hosts have random crystallographic orientation. Myrmekite development has been modelled from the P–T–t evolution of the ultramylonites, assuming that the development of the ultramylonites occurred during eo‐Alpine metamorphism at c. 450 °C, 7.5 kbar, followed by contact metamorphism at c. 530 °C, 2.75 kbar. Phase diagram pseudosections calculated from the measured bulk composition of granitic pegmatite protolith indicate that the equilibrium assemblage changes from Qtz–Phe–Ab ± Zo ± Cpx ± Kfs during the ultramylonite stage to Qtz–Pl(An_30–40)–Ms–Kfs–Bt(Ann₅₅) during the contact metamorphic stage. The thermodynamic prediction of increasing plagioclase mode and anorthite content, change of white mica composition and growth of biotite, occurring during the end of the heating path, are in agreement with the observed microstructures and analysed phase compositions of ultramylonites. Along with microstructural evidence, this supports the model that K‐feldspar replacement by myrmekite took place under static conditions, and was coeval with the static growth accompanying contact metamorphism. Myrmekite associated with muscovite can develop under prograde (up‐temperature) conditions in granites involved in polymetamorphism.     

Elemental mobility in subduction metamorphism: insight from metamorphic rocks of the Franciscan Complex and the Feather River ultramafic belt,California

The degree of element mobility in subduction metamorphism has generated much debate; some workers advocate considerable mobility during metamorphism, whereas others postulate minimal mobility. We assess this issue by examination of major and trace element concentrations and Pb-, Nd-isotopic data for 39 mafic metavolcanic rocks from the Franciscan subduction complex, related units of coastal California, and the Feather River ultramafic belt of the northern Sierra Nevada, California; these samples span a wide range of metamorphic grade. We conclude that these rocks, despite their metamorphism up to eclogite facies, preserve protolith major and trace elemental compositions and isotopic ratios, with the exception of some mobile large ion lithophile elements such as Ba, Pb, and to a smaller extent La, U, and Sr. Thus subduction metamorphism of these metabasalts occurred in a largely closed system. Lack of light rare earth element enrichment in the rocks demonstrates lack of chemical exchange with subducted metasediments. Relatively low SiO₂ content (<48 wt.%) of many of the metamorphic rocks and the lack of correspondence between silica depletion and metamorphic grade suggests that the silica depletion resulted from seafloor hydrothermal alteration before subduction. In spite of demonstrated mobility of Pb, and possible mobility of Nd, isotopic ratios of Pb and Nd were not modified during subduction metamorphism. In contrast to our results from metabasaltic rocks, our analysis of actinolite-rich rinds from high-grade Franciscan mélange blocks suggests some chemical exchange between metachert and the overlying mantle. The increasing enrichment in Ba and Pb with increasing metamorphic grade suggests that Ba- and Pb-rich fluids interacted more intensely with metabasalt at the higher grades of metamorphism. Comparison of these results with studies of the active Mariana forearc suggests that fluids interacting with the mantle wedge up-dip of the region of magma genesis are derived from subducting sediments overlying the down-going plate.     

Petrography and geochemistry of the Mesoarchean Bikoula banded iron formation in the Ntem complex (Congo craton), Southern Cameroon: Implications for its origin

Precambrian banded iron formations (BIFs) represent an important source of mineable iron, as well as an archive recording secular changes in the chemistry of the Earth’s early oceans. Here we report petrographic and geochemical characteristics of unweathered drill core samples from the Bikoula BIF, a virtually uncharacterized oxide facies iron formation, hosted in the Mesoarchean Ntem complex, southern Cameroon. The BIF is cross-cut with syenitic veins. The entire succession is highly deformed and metamorphosed under granulite facies conditions. The BIF is characterized by alternating micro-bands of magnetite, quartz and pyroxene. Sulfides (pyrite, pyrrhotite, and chalcopyrite), oligoclase, ferro-pargasite, biotite and ilmenite occur as minor phases. The presence of pyroxene, ferro-pargasite and oligoclase, relatively high contents of major elements such as Al₂O₃ (0.76–7.52 wt.%), CaO (1.95–4.90 wt.%), MgO (3.78–5.59 wt.%), as well as positive correlations among Al₂O₃, TiO₂, HFSEs, LILEs and transition metals (V, Cr, Ni, Cu and Zn), suggest that the BIF protolith included a significant amount of clastic material. Several samples have preserved seawater-like PAAS-normalized REE-Y patterns, including LREE depletion, and positive La and Y anomalies. Positive Eu anomalies observed in some of the analyzed samples indicate influx of hydrothermal fluids (possibly including Fe and Si) within the basin where the BIF precipitated. However, few samples show unusual negative Eu anomalies that likely result from a large proportion of clastic contamination. The lack of Ce anomalies suggests that the Bikoula BIF was deposited in a basin that was (at least partly) anoxic or suboxic, where it was possible to transport and concentrate dissolved Fe²⁺.     

Genesis for Rare Earth Elements Enrichment in the Permian Manganese Deposits in Zunyi,Guizhou Province,SW China

The Zunyi manganese deposits, which formed during the Middle to Late Permian period and are located in northern Guizhou and adjacent areas, are the core area of a series of large-medium scale manganese enrichment minerogenesis in the southern margin and interior of the Yangtze platform, Southern China. This study reports the universal enrichment of rare earth elements(REEs) in Zunyi manganese deposits and examines the enrichment characteristics, metallogenic environment and genesis of REEs. The manganese ore bodies present stratiform or stratoid in shape, hosted in the silicon–mud–limestones of the Late Permian Maokou Formation. The manganese ores generally present lamellar, massive, banded and brecciated structures, and mainly consist of rhodochrosite, ropperite, tetalite, capillitite, as well as contains paragenetic gangue minerals including pyrite, chalcopyrite, rutile, barite, tuffaceous clay rock, etc. The manganese ores have higher ΣREE contents range from 158 to 1138.9 ppm(average 509.54 ppm). In addition, the ΣREE contents of tuffaceous clay rock in ore beds vary from 1032.2 to 1824.5 ppm(average 1396.42 ppm). The REEs from manganese deposits are characterized by La, Ce, Nd and Y enriched, and existing in the form of independent minerals(e.g., monazite and xenotime), indicating Zunyi manganese deposits enriched in light rare earth elements(LREE). The Ce_(anom) ratios(average-0.13) and lithofacies and paleogeography characteristics indicate that Zunyi manganese deposits were formed in a weak oxidation-reduction environment. The(La/Yb)_(ch), Y/Ho,(La/Nd)_N,(Dy/Yb)_N, Ce/Ce* and Eu/Eu* values of samples from the Zunyi manganese deposits are 5.53–56.92, 18–39, 1.42–3.15, 0.55–2.20, 0.21–1.76 and 0.48–0.86, respectively, indicating a hydrothermal origin for the manganese mineralization and REEs enrichment. The δ~(13) C_(V-PDB)(-0.54 to-18.1‰) and δ~(18) O_(SMOW)(21.6 to 26.0‰) characteristics of manganese ores reveal a mixed source of magmatic and organic matter. Moreover, the manganese ore, tuffaceous clay rock and Emeishan basalt have extremely similar REE fractionation characteristic, suggesting REEs enrichment and manganese mineralization have been mainly origin from hydrothermal fluids.     

Petrography and geochemistry of Jurassic sandstones from the Jhuran Formation of Jara dome,Kachchh basin,India: Implications for provenance and tectonic setting

Sandstones of Jhuran Formation from Jara dome, western Kachchh, Gujarat, India were studied for major, trace and rare earth element (REE) geochemistry to deduce their paleo-weathering, tectonic setting, source rock characteristics and provenance. Petrographic analysis shows that sandstones are having quartz grains with minor amount of K-feldspar and lithic fragments in the modal ratio of Q ₈₉:F ₇:L ₄. On the basis of geochemical results, sandstones are classified into arkose, sub-litharenite, wacke and quartz arenite. The corrected CIA values indicate that the weathering at source region was moderate to intense. The distribution of major and REE elements in the samples normalized to upper continental crust (UCC) and chondrite values indicate similar pattern of UCC. The tectonic discrimination diagram based on the elemental concentrations and elemental ratios of Fe₂O₃ + MgOvs. TiO₂, SiO₂ vs. log(K₂O/Na₂O), Sc/Cr vs. La/Y, Th–Sc–Zr/10, La–Th–Sc plots Jhuran Formation samples in continental rift and collision settings. The plots of Ni against TiO₂, La/Sc vs. Th/Co and V–Ni–Th ?10 reveals that the sediments of Jhuran Formation were derived from felsic rock sources. Additionally, the diagram of (Gd/Yb) _N against Eu/Eu ^? suggest the post-Archean provenance as source possibly Nagar Parkar complex for the studied samples.     

Modal analysis and geochemistry of two sandstones of the Bhander Group (Late Neoproterozoic) in parts of the Central Indian Vindhyan basin and their bearing on the provenance and tectonics

The Neoproterozoic Bhander Group in the Son Valley, central India conformably overlying the Rewa Group, is the uppermost subdivision of the Vindhyan Supergroup dominantly composed of arenites, carbonates and shales. In Maihar-Nagod area, a thick pile of unmetamorphosed clastic sedimentary rocks of Bhander Group is exposed, which provides a unique opportunity to study Neoproterozoic basin development through provenance and tectonic interpretations. The provenance discrimination and tectonic setting interpretations are based on modal analysis and whole rock geochemistry. The average framework composition of the detrital sediments composed of quartz and sedimentary lithic fragments are classified as quartz arenite to sublitharenite. The sandstone geochemically reflects high SiO₂, moderate Al₂O₃ and low CaO and Na₂O type arenite. The high concentration of HFSE such as Zr, Hf, and Th/Sc, Th/U ratios in these sandstones indicate a mixed provenance. The chondrite normalized REE pattern shows moderate to strong negative Eu anomaly which suggests that major part of the sediments were derived from the granitic source area. The sandstone tectonic discrimination diagrams and various geochemical plots suggest that the provenance of the lower and upper Bhander sandstone formations was continental interior to recycled orogen.     

Petrographic and geochemical characteristics of Mesoproterozoic Kumbalgarh clastic rocks,NW Indian shield: implications for provenance,tectonic setting,and crustal evolution

The Kumbalgarh Group of the south Delhi fold belt are the main bedrock series exposed in the axial region of the Aravalli craton. Quartzites and greywackes, the chief clastic constituents of this group, are well exposed. Petrographic and bulk-rock analyses of these rocks permit determination of their provenance, tectonic setting of the basin, and the Archaean to Proterozoic crustal evolution. Greywackes comprise quartz, plagioclase, amphiboles, K-feldspar, and rock fragments. Based on mineralogy, we divided the quartzites into three categories: QTZ1 is chiefly composed of quartz with a silty matrix and a minor quantity of feldspars and QTZ2 contains significant mafic minerals as well as quartz and feldspars, whereas QTZ3 is more feldspathic than the other groups. All the lithounits have SiO₂/Al₂O₃ ratios <～10 suggesting textural immaturity consistent with their sedimentary petrography. Greywackes display the least fractionated rare earth elements (REEs) (La/Yb _N : avg. 2.55) with positive Eu anomalies (avg. Eu/Eu* = 1.34). QTZ1 contains strongly fractionated REE patterns (avg. La/Yb _N : 13.56, avg. Eu/Eu* = 0.60), QTZ2 shows moderate REE fractionation (avg. La/Yb _N : 4.97, avg. Eu/Eu* = 0.61), and QTZ3 possesses the least fractionated V-shaped REE patterns (avg. La/Yb _N : 1.97, avg. Eu/Eu* = 0.51). Weathering attributes including chemical index of alteration (CIA), plagioclase index of alteration (PIA), chemical index of weathering (CIW), and A–CN–K plots assign a low to moderate degree of weathering to the Kumbalgarh sediments under a subtropical climate. Based on our synthesis of the petrographic and geochemical data, we suggest a provenance comprising basalts, tonalite–trondhjemite–granodiorite (TTG), and granite. Geochemical attributes indicate deposition of the detritus in an extensional backarc basin receiving sedimentary input from opposite directions. The opening and then closure of the South Delhi Basin was the last phase of the break-up of the supercontinent, columbia, which began by abortive rifting of the Udaipur belt and culminated in separation of the Aravalli–Bundelkhand–Dharwar block in the east and the East African orogen in the west.     

Genesis of the Maanqiao gold deposit in the western Qinling orogen,central China: Constraints from fluid inclusions and in-situ sulfur isotopes

The western Qinling orogen (WQO) is one of the most important prospective gold provinces in China. The Maanqiao gold deposit, located on the southern margin of the Shangdan suture, is a representative gold deposit in the WQO. The Maanqiao deposit is hosted by the metasedimentary rocks of the Upper Devonian Tongyusi Formation. The EW-trending brittle-ductile shear zone controls the orebodies; they occur as disseminated, and auriferous quartz–sulfide vein. The ore-related hydrothermal alteration comprises silicification, sulfidation, sericitization, chloritization, and carbonatization. Native gold is visible and mainly associated with pyrite and pyrrhotite. Mineralization can be classified into the following three stages: bedding-parallel barren quartz–pyrite–(pyrrhotite) (early-stage), auriferous quartz–polymetallic (middle-stage), and carbonate–(quartz)–sulfide (late-stage).Detailed fluid inclusion (FI) studies revealed three types of inclusions in quartz and calcite: aqueous (W-type), CO₂–H₂O (C-type), and pure carbonic (PC-type) FIs. The primary FIs in the early-stage quartz are C- and PC-type, in the middle-stage quartz are mainly W- and C-type, and in the late-stage calcite are only W-type. During gold mineralization, the total FI homogeneous temperatures evolved from 189–375 °C (mostly 260–300 °C) to 132–295 °C (mostly 180–240 °C) to 123–231 °C (mostly 130–150 °C), and the salinities varied among 2.2–9.1 wt.% NaCl equiv. (mostly 5–8 wt.%) to 0.2–9.0 wt.% NaCl equiv. (mostly 3–6 wt.%) to 0.3–3.6 wt.% NaCl equiv. (mostly 2–4 wt.%). The ore-forming fluid was characterized as an H₂O–NaCl−CO₂−CH₄–(N₂) system with medium-low temperature and low salinity. The fluid immiscibility and fluid-rock interaction may be responsible for the precipitation of the sulfides and gold at the Maanqiao gold deposit. Three types of pyrite corresponding to the three mineralization stages, as well as pyrrhotite and arsenopyrite in the middle stage, are micro-analyzed for in-situ sulfur isotopic composition by LA-ICP-MS. Py1 yield near-zero δ³⁴S values of −2.5‰ to 3.0‰, which are somewhat lower than that of the granite hosted pyrites (Py-g, 4.8‰ to 6.6‰). The result suggests a mixed sulfur source from magmatic-hydrothermal fluids and the metamorphism of diagenetic pyrite. Pyrite + pyrrhotite + arsenopyrite assemblages in the middle-stage have relatively higher δ³⁴S values (6.6‰ to 12.3‰) and are mainly developed due to the metamorphism of the ore-host and underlying Devonian sedimentary sequences. The low δ³⁴S values of the late-stage fracture-filled Py3 (−21.9‰ to −17.0‰) resulted from an increasing oxygen fugacity, which was caused by the inflow of oxidized meteoric waters.Based on our studies, the Maanqiao gold deposit is considered to be an orogenic type and closely related to the Indosinian Qinling orogeny.