Sources of stream sediments in the granulite terrain of the Walawe Ganga Basin,Sri Lanka,indicated by rare earth element geochemistry

Thirty-eight samples of stream sediments draining high-grade metamorphic rocks in the Walawe Ganga (river) Basin, Sri Lanka, were analysed for their REE contents, together with samples of metamorphic suites from the source region. The metamorphic rocks are enriched in light REE (LREE) compared to heavy REE (HREE) and are characterised by high La/Lu ratios and negative Eu anomalies. The chondrite-normalised patterns for these granulite-grade rocks are similar to that of the average post-Archaean upper crust, but they are slightly enriched with La and Ce. The REE contents of the <63-μm fraction of the stream sediments are similar to the probable source rocks, but the other grain size fractions show more enriched patterns. The <63-μm stream sediments fraction contains lower total REE, more pronouncd negative Eu anomalies, higher Eu_N/Sm_N and lower La _N/Lu_N ratios relative to other fractions. The lower La _N/Lu_N ratio is related to the depletion of heavy minerals in the <63-μm fraction. The 63–125-μm and 125–177-μm grain size fractions of sediments are particularly enriched in LREE (average ΣLREE=2990 μg/g and 3410 μg/g, respectively). The total HREE contents are surprisingly uniform in all size fractions. However, the REE contents in the Walawe Ganga sediments are not comparable with those of the granulite-grade rocks from the source region of the sediments. The enrichment of REE is accounted for by the presence of REE containing accessory mineral phases such as zircon, monazite, apatite and garnet. These minerals are derived from an unknown source, presumably from scattered bodies of granitic pegmatites.     

Application of multi-element relationships in stream sediments to mineral exploration: a case study of Walawe Ganga Basin,Sri Lanka

This study on the application of multi-element relationships in stream sediments to mineral exploration in the Walawe Ganga Basin presents one of the first of its kind in Sri Lanka. In order to determine the nature of these sediments, multi-element analysis of selected grain size (<63 μm, 63–125 μm, 125–177 μm and 177–250 μm) fractions was undertaken. The chemical composition of these fractions were compared with those of the upper continental crust.Some elements, notably Zr, Hf, Th, U, Ce and La, show very high enrichment factors (e.g. 54 for Zr) as compared to the upper crustal abundance. These are presumably associated with heavy minerals such as zircon, rutile and monazite found in abundance in the stream sediments of the Walawe Ganga Basin.Principal Component Analysis (PCA) of the geochemical data show that multi-element relationships could be effectively used to delineate target areas for mineral exploration. With the use of PCA, this study reveals that areas with associations of calc-silicate/marble and charnockitic rocks are probable source regions for mineral occurrences, particularly in the axial regions of anticlines.     

The geochemistry of beryllium and fluorine in the gem fields of Sri Lanka

A study of the abundance of Be in the gem sediments of Sri Lanka shows that Be is found in the range of 1–13 ppm. Be shows an irregular distribution among sediments. It occurs in the silicate form and due to the proximity to the beryllium bearing rocks, namely granites and pegmatites of the Highland and Southwest Groups of Sri Lanka, very little decomposition of the Be-bearing minerals had taken place. This is further aided by the high resistance to weathering of the beryllium minerals, particularly beryl and chrysoberyl.The beryllian granites and pegmatites of the Precambrian of Sri Lanka are presumed to have been formed due to the magmatic activity associated and related to charnockitic rocks abundant in the main gem bearing areas of Sri Lanka.Fluorine is found in the range of 400–2,000 ppm and the F/Be ratios for all the areas studied show a range of 54–441. The analysis of the averages of these ratios do not show any particular anomaly in any of the areas studied. The narrow ranges of the F/Be ratios indicate the similar conditions under which weathering and geochemical transportation had taken place in the gem fields of Sri Lanka.     

Major and trace element geochemistry in upper Ganga river in the Himalayas, India

Chemical weathering and resulting water compositions in the upper Ganga river in the Himalayas were studied. For the first time, temporal and spatial sampling for a 1 year period (monthly intervals) was carried out and analyzed for dissolved major elements, trace elements, Rare Earth Elements (REE), and strontium isotopic compositions. Amounts of physical and chemical loads show large seasonal variations and the overall physical load dominates over chemical load by a factor of more than three. The dominant physical weathering is also reflected in high quartz and illite/mica contents in suspended sediments. Large seasonal variations also occur in major elemental concentrations. The water type is categorized as HCO₃^––SO₄^2––Ca²⁺ dominant, which constitute >60% of the total water composition. On an average, only about 5–12% of HCO₃^– is derived from silicate lithology, indicating the predominance of carbonate lithology in water chemistry in the head waters of the Ganga river. More than 80% Na⁺ and K⁺ are derived from silicate lithology. The silicate lithology is responsible for the release of low Sr with extremely radiogenic Sr (⁸⁷Sr/⁸⁶ Sr>0.75) in Bhagirathi at Devprayag. However, there is evidence for other end-member lithologies for Sr other than carbonate and silicate lithology. Trace elements concentrations do not indicate any pollution, although presence of arsenic could be a cause for concern. High uranium mobilization from silicate rocks is also observed. The REE is much less compared to other major world rivers such as the Amazon, perhaps because in the present study, only samples filtered through <0.2 m were analysed. Negative Eu anomalies in suspended sediments is due to the excess carbonate rock weathering in the source area.     

中国云南哀牢山含海蓝宝石伟晶岩的起源和成岩模拟实验研究

The Ailaoshan aquamarine-bearing pegmatites are associated with Proterozoic metamorphic rocks in the southern portion of the Ailaoshan fault-folded complex.The gem-bearing pegmatite mineralization zones of the region occur in areas generally consistent with the regional tectonic trend.The pegmatites are found in metamorphic rocks,migmatites and in the inner/outer contact zones of gneissoid granites. The Rb-Sr isochron drawn for the pegmatites is 26～31 Ma,(i.e.in Himalayan).The homogenization temperatures of melt and liquid inclusions in minerals vary from 185 to 920℃,which are comparable to the inclusions observed in banded migmatites and ptygmatic quartz veins in the surrounding metamorphic rocks. The mineralization fluids of the pegmatite were rich in HCO_3 and CO_2,and their compositional assemblages are comparable to metamorphic fluids.Results of H,O,C,Si etc.isotopic analyses and REE,and Be analyses indicates that the sources of mineralization components that formed the pegmatites are closely associated with metamorphic fluids and the enclosing metamorphic rocks. A pegmatite structure simulation experiment was conducted at high temperature and pressure(840℃and 1,500×105Pa.),with various metamorphic rock samples in a water-rich and volatile-rich environment.When the liquidus was reached,the temperature was gradually decreased at the rate of 5～10℃/day over a time period of three months.SEM energy-dispersive spectrum analyses were performed on the experimental products.A series of pegmatoid textures were observed including zonal texture,megacryst texture,drusy cavities,crystal druses,and vesicular texture along with more than ten types of minerals including plagioclase,microcline,quartz and biotite.Different metamorphic rock melts generated different mineral assemblages.Experiment results revealed that the partial melting of metamorphic rocks could form melts similar to pegmatite magmas. Based upon the geological characteristics,geochemistry,and pegmatite texture simulation experimental results,it is concluded that the mineralization components of Ailaoshan aquamarine-bearing pegmatites came from metamorphic rocks.The petrogenetic model for the origin of pegmatites is related to ultrametamorphism and metamorphic anatexis.     

Dahab stream sediments, southeastern Sinai, Egypt: a potential source of gold, magnetite and zircon

The stream sediments of Dahab area, southeastern Sinai, Egypt, were studied for their content of economic minerals. These sediments are immature as indicated by poor sorting and other mechanical parameters. They are derived from Precambrian basement rocks, which are mostly represented by granitic rocks in addition to lesser amounts of volcanics and gabbros. The mineralogical investigation revealed that these sediments contain considerable amounts of placer gold, Fe–Ti oxides and zircon.The concentrated Fe–Ti oxides comprise homogeneous magnetite and ilmenite in addition to ilmeno-magnetite, hemo-ilmenite and rutile–hematite intergrowths. Isodynamic separation of some raw samples of SIZE=1 mm revealed that up to 15.12% magnetic minerals can be recovered. Zircon shows remarkable variations in morphology, colour, chemistry and provenance. U-poor and U-rich varieties of zircon were discriminated containing UO₂ in the ranges of 0.04–1.19 and 3.05–3.68 wt.%, respectively. REE-bearing minerals comprise monazite, allanite and La-cerianite.On mineralogical basis, the present work suggests that Dahab stream sediments represent a promising target for further geochemical exploration for precious metals, especially gold. Fire assay data indicate that placer gold in the studied sediments sometimes reaches 15.34 g/t. Narrow gullies and valleys cutting the basement manifest the development and preservation of gold in this arid environment. Background concentration of gold and variation in lithology suggest multiple source of the metal in the investigated sediments.     

Geochemistry and provenance of stream sediments of the Ganga River and its major tributaries in the Himalayan region,India

Major, trace and REE compositions of sediments from the upper Ganga River and its tributaries in the Himalaya have been examined to study the weathering in the Himalayan catchment region and to determine the dominant source rocks to the sediments in the Plains. The Ganga River rises in the Higher Himalaya from the Higher Himalayan Crystalline Series (HHCS) bedrocks and traverses over the Lesser Himalayan Series (LHS) and the Himalayan foreland basin (Siwaliks) rocks before entering into the Gangetic Plains. The major element compositions of sediments, reflected in their low CIA values (45.0–54.7), indicate that silicate weathering has not been an important process in the Himalayan catchment region of the Ganga River. Along the entire traverse, from the HHCS through LHS and the Siwaliks, the sediments from the tributaries and the mainstream Ganga River show higher Na₂O, K₂O, CaO and silica. This, and the higher ratios of La/Sc, Th/Sc and lower ratios of Co/Th, suggest that the source rocks are felsic. The fractionated REE patterns and the significant negative Eu anomalies (Eu/Eu? = 0.27–0.53) indicate highly differentiated source. Moreover, the comparison of the sediments with different source rock lithologies from the HHCS and the LHS for their major elements clearly suggests that the HHCS rocks were the dominant source. Further, comparison of their UCC (upper continental crust) normalized REE patterns suggests that, among the various HHCS rocks, the metasediments (para-gneiss and schist) and Cambro-Ordovician granites have formed the major source rocks. The Bhagirathi and Alaknanda River sediments are dominantly derived from metasediments and those in the Mandakini River from Cambro-Ordovician granites. The resulting composition of the sediments of the Ganga River is due to the mixing of sediments supplied by these tributaries after their confluence at Devprayag. No further change in major, trace and rare earth element compositions of the sediments of the Ganga River after Devprayag up to its exit point to the Plains at Haridwar, suggests little contribution of the Lesser Himalayan and Siwalik rocks to the Ganga River sediments.     

Geochemistry of Mansar Lake sediments, Jammu, India: Implication for source-area weathering, provenance, and tectonic setting

The sediment geochemistry, including REE, of surface and core samples from Mansar Lake, along with mineralogical investigations, have been carried out in order to understand the provenance, source area weathering, hydrolic sorting and tectonic setting of the basin. The geochemical signatures preserved in these sediments have been exploited as proxies in order to delineate these different parameters.The major element log values (Fe₂O₃/K₂O) vs (SiO₂/Al₂O₃) and (Na₂O/K₂O) vs (SiO₂/Al₂O₃) demarcate a lithology remarkably similar to that exposed in the catchment area. The chondrite normalized REE patterns of lake samples are similar to Post Archaean Australian Shale (PAAS) with LREE enrichment, a negative Eu anomaly and almost flat HREE pattern similar to a felsic and/or cratonic sedimentary source. However, the La–Th–Sc plot of samples fall in a mixed sedimentary domain, close to Upper Continental Crust (UCC) and PAAS, suggesting sedimentary source rocks for the Mansar detritus. It also indicates that these elements remained immobile during weathering and transportation. The mineralogical characteristic, REEs, and high field strength elements (HFSE), together with the high percentage of metamorphic rock fragments in the Siwalik sandstone, support a metamorphic source for lower Siwalik sediments. A very weak positive correlation between Zr and SiO₂, poor negative correlation with Al₂O₃, negative correlation of (La/Yb)_N and (Gd/Yb)_N ratios with SiO₂ and positive correlation with Al₂O₃, suggest that Zr does not dominantly control the REE distribution in Mansar sediments. The petrographic character and textural immaturity indicate a short distance transport for the detritus. The distribution of elements in core samples reflect fractionation. The higher Zr/Th and Zr/Yb ratios in coarse sediments and PAAS compared to finer grained detritus indicate sedimentary sorting. Plots of the geochemical data on tectonic discrimination diagrams suggest that the sediments derived from the lower Siwalik were originated within a cratonic interior and later deposited along a passive margin basinal setting. It therefore reveals lower Siwalik depositional history.     

The nature of fluids during pegmatite development in metamorphic terrains: Evidence from Hamadan complex,Sanandaj-Sirjan metamorphic zone,Iran

In the Sanandaj-Sirjan zone of metamorphic belt of Iran, the area south of Hamadan city comprises of metamorphic rocks, granitic batholith with pegmatites and quartz veins. Alvand batholith is emplaced into metasediments of early Mesozoic age. Fluid inclusions have been studied using microthermometry to evaluate the source of fluids from which quartz veins and pegmatites formed to investigate the possible relation between host rocks of pegmatites and the fluid inclusion types. Host minerals of fluid inclusions in pegmatites are quartz, andalusite and tourmaline. Fluid inclusions can be classified into four types. Type 1 inclusions are high salinity aqueous fluids (NaCl_eq >12 wt%). Type 2 inclusions are low to moderate salinity (NaCl_eq <12 wt%) aqueous fluids. Type 3 and 4 inclusions are carbonic and mixed CO₂-H₂O fluid inclusions. The distribution of fluid inclusions indicate that type 1 and type 2 inclusions are present in the pegmatites and quartz veins respectively in the Alvand batholith. This would imply that aqueous magmatic fluids with no detectable CO₂ were present during the crystallization of these pegmatites and quartz veins. Types 3 and 4 inclusions are common in quartz veins and pegmatites in metamorphic rocks and are more abundant in the hornfelses. The distribution of the different types of fluid inclusions suggests that CO₂ fluids generated during metamorphism and metamorphic fluids might also contribute to the formation of quartz veins and pegmatites in metamorphic terrains.     

The gold content of some Archaean rocks and their possible relationship to epigenetic gold-quartz vein deposits

Gold mineralization in Archaean granite-greenstone environments, especially gold-quartz veins, contributes considerably to the world's gold production. The formation of epigenetic gold mineralization in greenstone belts is generally explained by the metamorphic secretion theory. This theory is based on the assumption that the source of the gold may be komatiitic or tholeiitic lavas, pyritic chemical or clastic sediments and even granitic rocks from which, as a result of regional metamorphic overprinting, gold was extracted and concentrated in suitable structures.It has been shown that in proposed potential source rocks, gold is predominantly associated with sulfide minerals and thus relatively easily accessible to secretion and reconstitution processes.A large number of various rock types originating from granite-greenstone terranes of the Kaapvaal and the Rhodesian cratons were geochemically investigated, and the following ranges for gold determined:volcanic rocks (komatiitic and tholeiitic): 0.1–372 ppbgranitic rocks of the basement: 0.3–7.8 ppbiron-rich chemical sediments: 1.0–667 ppbStatistical treatment of the data reveals that volcanic rocks as well as iron-rich chemical sediments are favorable sources for epigenetic gold mineralization formed by metamorphic secretion, while the granitic rocks make less suitable primary gold sources. This finding explains the close spatial relationship which is common between gold-quartz veins and greenstone belts. The conspicuous abundance of epigenetic gold mineralization in the Archaean, however, is attributed to the unique geologic and metamorphic history of the granite-greenstone terranes.     

Geochemistry of coastal sands of Eastern Mediterranean: The case of Nisyros volcanic materials

Coastal sand samples collected from the northern part of Nisyros volcanic island (Dodecanese, Greece) were investigated for first time for their potential in strategic metals and compared with parental rocks of the island which are Quaternary volcanics with alternating lava flows, pyroclastic layers and lava domes and relevant materials located near granitoids of Northern Greece. The PXRD and SEM-EDS study of the sands revealed enhanced content of feldspars, Fe-Mn oxides, magnetite, tourmaline, pyroxenes, ilmenites, along with zircons, apatite and sulfide inclusions. The fresh hydrothermally deposited clayely material collected from the Nisyros caldera crater had a rather different mineralogical composition from the coastal one (alunite, anhydrite, opal-CT, quartz, kaolinite). UCC-normalized spidergrams indicated that the weathering processes contributed to accumulation of heavy minerals (mainly ilmenite), and strategic metals including V (1920 mg/kg) and Nb (245 mg/kg), in the coastal sand. The low REE concentration (ΣREE + Y = 240 mg/kg) could be attributed to the absence of REE-rich minerals. Moreover, the sands exhibit different geochemical patterns compared to the volcanic source rocks of the island, which are especially enriched in Large-Ion Lithophile Elements (LILE) and depleted in High Field Strength Elements (HFSE), such as Nb and Ta. On the other hand, the caldera material is enriched in volatile components, sulfur, chalcophile elements (Se, Bi, Hg, As, Pb) and Ba. Micro-XRF analyses of representative crystals showed that the high Nb content of the sands was associated with the Ti/Fe-rich phases (e.g. ilmenites). The geochemical composition of N Greece sands showed, because of their origin, enrichment not only in HFSE but also in REE.The study of the coastal heavy mineral sands originating from different geological environments of Greece provides information about the association of their mineral components with REE, other elements of economic interest (e.g. Co, Nb, Ta) and natural actinides. In addition, the study of the black sands of Nisyros island could be considered as a characteristic example of those from other parts of Hellenic Volcanic Arc (HVA) and other relevant Mediterranean regions.     

Traceurs sédimentaires des variations du niveau marin et de la mousson sud-est asiatique depuis 450 ka en mer de Chine du Sud

In order to reconstruct the past variations of the Southeast Asian monsoon intensity and estimate the sedimentary system reactivity to climatic changes in Southeast Asia over the last 450 kyr, mineralogical and sedimentological analyses have been performed on the terrigenous fraction of the South China Sea sediment. End-member modelling coupled with grain size data discriminates three end-members that determine the nature and intensity of the main sediment transport vectors. Low sea-level stands are characterized by sediment reworking that allows transportation of a coarse end-member (20–40 μm) to the deep-basin. By contrast, the other end-members (4–6 μm; 9–13 μm) are controlled by the shoreline position (sea level) and/or by changes of the rivers capacity transport (monsoon). Finally, aeolian input to the northern margin of the South China Sea can be considered negligible compared to the massive fluvial input and the reworking of the sediments.     

Evolution of the Yunkai Terrane, South China: Evidence from SHRIMP zircon U–Pb dating, geochemistry and Nd isotope

The Yunkai Terrane is one of the most important pre-Devonian areas of metamorphosed supracrustal and granitic basement rocks in the Cathaysia Block of South China. The supracrustal rocks are mainly schist, slate and phyllite, with local paragneiss, granulite, amphibolite and marble, with metamorphic grades ranging from greenschist to granulite facies. Largely on the basis of metamorphic grade, they were previously divided into the Palaeo- to Mesoproterozoic Gaozhou Complex, the early Neoproterozoic Yunkai ‘Group’ and early Palaeozoic sediments. Granitic rocks were considered to be Meso- and Neoproterozoic, or early Palaeozoic in age. In this study, four meta-sedimentary rock samples, two each from the Yunkai ‘Group’ and Gaozhou Complex, together with three granite samples, record metamorphic and magmatic zircon ages of 443–430 Ma (Silurian), with many inherited and detrital zircons with the ages mainly ranging from 1.1 to 0.8 Ga, although zircons with Archaean and Palaeoproterozoic ages have also been identified in several of the samples. A high-grade sillimanite–garnet–cordierite gneiss contains 242 Ma metamorphic zircons, as well as 440 Ma ones. Three of the meta-sedimentary rocks show large variations in major element compositions, but have similar REE patterns, and have t_DM model ages of 2.17–1.91 Ga and ε_Nd (440 Ma) values of −13.4 to −10.0. Granites range in composition from monzogranite to syenogranite and record t_DM model ages of 2.13–1.42 Ga and ε_Nd (440 Ma) values of −8.4 to −1.2. It is concluded that the Yunkai ‘Group’ and Gaozhou Complex formed coevally in the late Neoproterozoic to early Palaeozoic, probably at the same time as weakly to un-metamorphosed early Palaeozoic sediments in the area. Based on the detrital zircon population, the source area contained Meso- to Neoproterozoic rocks, with some Archaean material. Palaeozoic tectonothermal events and zircon growth in the Yunkai Terrane can be correlated with events of similar age and character known throughout the Cathaysia Block. The lack of evidence for Palaeo- and Mesoproterozoic rocks at Yunkai, as stated in earlier publications, means that revision of the basement geology of Cathaysia is necessary.     

Textures and phase relationships in ferrous granulites from Tidjenouine (Hoggar, Algeria): fayalite–ferrossilite–quartz secondary assemblage

Ferrous granulites in the area of Tidjénouine (Central Hoggar) exhibit a remarkable mineralogical composition characterized by the association orthoferrossilite–fayalite–quartz. These granulites are metamorphosed mafic igneous rocks showing the juxtaposition of different metamorphic parageneses. Peak paragenesis with garnet–clinopyroxene–amphibole–plagioclase–quartz reach to assemblage with orthopyroxene–plagioclase₂. Secondary orthopyroxene reacted with garnet to produce symplectites with fayalite + plagioclase + quartz. The latest stage corresponds to an orthopyroxene–fayalite–quartz–plagioclase assemblage. The metamorphic history of the ferrous granulites is inferred by combining the study of phase relations with the construction of a petrogenetic grid and pseudosection in the CFMASH and CFAS systems using the Thermocalc program of [J. Metamorph. Geol. 6 (1988) 173]. The evolution of paragenetic minerals indicates a metamorphic P–T path through the following conditions: 7.1 ± 1 kbar at 880 °C, 4.9 ± 1.6 kbar at 750 °C and 3–4 kbar at 700 °C, which is consistent with a clockwise P–T path recorded throughout the area.     

Discovery of a c.370 Ma granitic gneiss clast from the Hwanggangri pebble-bearing phyllite in the Okcheon metamorphic belt, Korea

The chemical Th–U total Pb isochron method (CHIME) of dating was carried out on accessory minerals in samples from the Okcheon metamorphic belt in Korea. Dated minerals include xenotime and monazite with overgrown mantles in a granitic gneiss clast from the Hwanggangri Formation, metamorphic allanite in garnet-bearing muscovite–chlorite schist of the Munjuri Formation, and polycrase and monazite in post-tectonic granite from the Hwanggangri area. Overgrowth of mantles took place at 369 ± 10 Ma on c. 1750 Ma cores of xenotime and monazite in the granitic gneiss. Allanite, occurring in textural equilibrium with peak metamorphic minerals, yields a CHIME age of 246 ± 15 Ma that is discriminably older than the polycrase (170 ± 6 Ma) and monazite (170 ± 3 Ma) ages of the post-tectonic granite. These chronological data suggest that some of the metasedimentary rocks in the belt formed through a single stage of metamorphism at c. 250 Ma from post-370 Ma sediments. Late Permian age signatures have also been reported from the Precambrian Gyeonggi and Yeongnam massifs that border the Okcheon metamorphic belt, and indicate that parts of the basement massifs and the metamorphic belt were affected by the same regional metamorphic event.     

Rare earth element mobility during prograde granulite facies metamorphism: significance of fluorine

 Mafic gneisses occur as lenses or thin layers in spatial association with tonalitic leucosomes in a granulite zone of the Quetico subprovince of the Superior Province, Ontario, Canada, and exhibit concentric zoning with a biotite-rich margin, orthopyroxene-rich outer zone, clinopyroxene-rich central zone, and, occasionally, patches of relict amphibolites within the clinopyroxene-rich zone. The granulites (biotite-, orthopyroxene- and clinopyroxene-rich zones) in the mafic gneisses are characterized by significant amounts of rare earth element (REE)-bearing fluorapatite (1–10 vol.%) and other REE-rich minerals (allanite, monazite and zircon). Fluorapatite shows an increase in modal abundance from the biotite- and orthopyroxene-rich zones to the clinopyroxene-rich zone, but is rare in the relict amphibolites. Textural evidence and element partitioning indicate that fluorapatite (and other REE-rich minerals) was part of the peak metamorphic assemblages. Whole-rock geochemical analyses confirm that the granulites in the mafic gneisses contain anomalously high contents of REE and high field strength elements (HFSE), whereas the relict amphibolites are geochemically typical of tholeiitic basalts. Mass-balance calculations reveal that REE and HFSE were introduced into the mafic gneisses during the prograde granulite facies metamorphism, pointing to REE mobility under granulite facies metamorphic conditions. The presence of high F contents in the REE-rich minerals and their associated minerals (e.g. biotite and hornblende) suggests that REE and HFSE may have been transported as fluoride complexes during the granulite facies metamorphism. This conclusion is supported by previously published results of hydrothermal experiments on the partitioning of REE between fluorapatite and F-rich fluids at 700°C and 2 kbar. Received: 2 May 1995 / Accepted: 28 September 1995     

A new simple approach to evaluate pedogenic clay transformation in a Vertic Calcisol

The aim of this study is to characterize the pedogenic clay minerals by using simple approach: mixing mineralogical and geochemical findings.The fine clay fractions (< 0.1 μm) of a Vertic Cambisol profile were studied by means of X-ray diffraction (XRD), infrared spectroscopy (FTIR) and cation exchange capacity (CEC).Qualitative and quantitative mineralogical compositions of the clay mixture were determined.Moreover, chemical equilibria and thermodynamic stabilities of minerals (calcite, gypsum, kaolinite, smectites and illites) were studied using results of ionic activities obtained from total concentration of various aqueous species in water extracts from soil-saturated pastes.XRD analysis shows a good homogeneity in the mineralogical composition of the soil material, with depth of soil profiles. The identified clay minerals are mainly illite–smectite mixed layers (I/S) and kaolinite. The chemical analysis of saturated paste extracts with clay minerals shows a slight undersaturation of the illitic phase while smectites and also calcite and gypsum reach the thermodynamic equilibrium along the soil profile.     

赣南新元古代变质岩稀土矿物及其地球化学特征

近年来赣南地区首次报道了变质岩离子吸附型稀土矿床的发现,为离子吸附型稀土的找矿提供了新思路。赣南地区新元古代变质岩大面积分布,风化壳也广泛发育。文章对30件稀土元素含量(300×10~(-6))高的变质岩矿物样品进行了详细的电子探针分析,旨在查明赣南新元古代不同类型变质岩中的稀土矿物种类及特征,探讨其成因、对全岩稀土元素含量的贡献以及离子吸附型稀土元素的成矿潜力。研究表明,区域上变质岩可大致分为6类,分别是变质凝灰岩类、板岩类、千枚岩类、片岩类、变砂岩类和变粒岩类,不同类型变质岩的稀土矿物组合不同,除了普遍存在的、难风化的独居石、磷钇矿和锆石外,部分岩性中出现易风化的褐帘石、含稀土元素绿泥石和含稀土元素金红石,及表生的水磷酸盐和磷铝酸盐等矿物。这些富稀土矿物贡献了全岩中大部分稀土元素,且部分矿物成因与后期流体作用相关,为成矿提供了良好的条件。文章总结分析认为,赣南地区广泛分布的变质岩中,片岩类、变砂岩类和变质凝灰岩类均具有相对易风化的稀土矿物组合,尤其变质凝灰岩类和变砂岩类,能为离子吸附型稀土成矿提供充足的物质来源,具有可观的离子吸附型稀土成矿潜力。     

Mineralogical and chemical evolution of tantalum–(niobium–tin) mineralisation in pegmatites and granites. Part 2: Worldwide examples (excluding Africa) and an overview of global metallogenetic patterns

Columbite-group minerals (CGM) account for the majority of the production of tantalum, an important metal for high-technology applications. Along with other Ta–Nb oxides such as tapiolite, wodginite, ixiolite and pyrochlore supergroup minerals, CGM are recovered from rare-metal granites and granitic rare-element pegmatites. In this paper mineralogical and geochemical data with a focus on CGM, tapiolite, wodginite and ixiolite are presented for rare-element granites and pegmatites from worldwide occurrences except Africa that has been covered in a previous contribution (Melcher et al., 2015). Major and trace element data of the Ta–Nb oxides are presented and compared for a total of 25 granite/pegmatite provinces, and one carbonatite for comparison. Based on CGM compositions, the data allow to distinguish between various subgroups of Li–Cs–Ta (LCT)-family pegmatites, Nb–Y–F (NYF)-family pegmatites, mixed LCT–NYF pegmatites, and rare-element granites.Each period of Ta-ore formation in Earth history is characterised by peculiar mineralogical and geochemical features. Some of the largest and economically most important rare-element pegmatite bodies are located within Archean terrains and intruded ultramafic and mafic host rocks (e.g., Tanco/Canada, Wodgina and Greenbushes/Western Australia, Kolmozero/Kola). They are highly fractionated, of LCT affinity throughout and yield complex mineralogical compositions. The variety of minor and trace elements incorporated attests to a rather insignificant role of the immediate host rocks to their geochemical signature and rather points to the significance of the composition of the underlying crustal protoliths, internal fractionation and the processes of melt generation. Many of the Archean pegmatites carry significant Li mineralization as spodumene, petalite, and amblygonite, and all of them are also characterised by elevated Li in CGM. In addition, Sb and Bi are important trace elements, also reflected by the occasional presence of stibiotantalite and bismutotantalite. REE_N patterns of CGM are dominated by the MREE or HREE, and range from very low to high total REE concentrations. Negative Eu anomalies are omnipresent. Scandium contents are also highly variable, from very high (Tanco) to very low concentrations (Wodgina, Kolmozero).A second period of worldwide pegmatite formation was in the Paleoproterozoic. All CGM analysed derive from LCT-family pegmatites except samples from the Amazonas region where Ta is mined from rare-metal granites at Pitinga. Pegmatites intruded highly variable lithologies including metasediments, metabasites, gneiss, granite and quartzite within a variety of structural and paleogeographic settings; however, most of them are syn- to post-orogenic with respect to major Paleoproterozoic orogenic events. Minor and trace element signatures are similar to CGM from Archean pegmatites. Some are characterised by considerable REE enrichment (São João del Rei/Brazil; Amapá/Brazil; Finnish Lapland/Finland), whereas others have normal to low total REE concentrations (Black Hills/USA, Bastar/India). Examples with high REE commonly are enriched in Sc and Y as well, and are often transitional to NYF-family pegmatites.The Mesoproterozoic period is comparatively poor in rare-element pegmatites and rare-metal granites. Mineralogical and chemical attributes of ixiolite–wodginite, tapiolite, CGM and rutile from placer material in Colombia point to an unusual pegmatite source of NYF affinity, yielding high total REE, Sc and Th at low Li and Bi. REE patterns have typical negative Eu and Y anomalies.A third major period of pegmatite formation was the Early Neoproterozoic at around 1 Ga, documented in the Grenvillian (North America), the Sveconorwegian (northern Europe) and the Kibaran in central Africa. CGM are present in numerous, mostly small pegmatites, although larger examples also occur (e.g., Manono in the D.R. Congo; Melcher et al., 2015). Pegmatite fields often display a zonal arrangement of mineralised pegmatites with respect to assumed “fertile” parent granites. They intrude metasediments, metabasites, gneiss and granite of middle to upper crustal levels and display a variety of mineralogical and chemical characteristics. Pegmatites of the Sveconorwegian and Grenville domains are usually of the NYF type and CGM are characterised by elevated Y, REE, Th and Sc. In contrast, the pegmatites of central (Kibara Belt) and southwestern Africa (Orange River Belt) are commonly of LCT affinity carrying spodumene, beryl and cassiterite (Melcher et al., 2015). These CGM have elevated conce ntrations of Li, Mg, Sn and Hf. Total REE concentrations are low except for the Sveconorwegian, and exhibit a variety of shapes in normalised diagrams.The fourth major pegmatite-forming event coincides with amalgamation of Gondwana at the Neoproterozoic/Paleozoic boundary around 550 Ma ago. This event is omnipresent in Africa (“Panafrican”) and South America (“Brasiliano event” documented in the Eastern Brazilian pegmatite and Borborema provinces). Pegmatites often intruded high-grade metamorphic terrains composed of metasediments including schist, marble, quartzite, as well as gneiss, amphibolite, ultramafic rocks, and granite. Within the Neoproterozoic, rare-metal granites of NYF affinity are locally abundant. Pegmatites show both LCT and NYF affinities, and mixed types occur in Mozambique. The Alto Ligonha and Madagascar provinces are characterised by abundant REE and Sc both within Ta–Nb-oxides and as separate mineral phases. Notably, some pegmatite provinces are almost devoid of cassiterite, whereas others carry cassiterite in economic amounts.In the Phanerozoic (younger than 542 Ma), pegmatites formed at all times in response to orogenetic processes involving various continents and terranes during the long-time amalgamation of Pangea and the Alpine orogenies. Whereas some activity is related to the Pampean, Acadian and Caledonian orogenies, the Variscan/Hercynian and Alleghanian orogenies are of utmost importance as manifested in pegmatite formation associated with Sn–W mineralised granites in central and western Europe as well as in the Appalachians. Most of the Variscan and Alleghanian pegmatites are of LCT affinity, although NYF and some mixed types have been described as well. Variscan pegmatite formation culminated at ca. 330 to 300 Ma, whereas Alleghanian pegmatites range in age from about 390 Ma to about 240 Ma. Most are syn- to post-orogenic and were emplaced at different crustal levels and into a variety of host rocks. Degree of fractionation as well as minor and trace element geochemistry of Ta–Nb oxides are rather variable and cover the complete field of CGM compositions. REE patterns are characterised by prominent negative Eu anomalies.Some Mesozoic and Cenozoic pegmatites and rare-metal granites from Southeast Asia and the Russian Far East are included in the compilation. Rare-metal granites of the Jos Plateau (Nigeria) were previously investigated (Melcher et al., 2015). The proportion of NYF pegmatites and rare-metal granites in the Mesozoic is striking, i.e. illustrated by Jos, Orlovka, Ulug Tanzek as well as the southeast Asian deposits related to tin granites. CGM from these areas are invariably rich in REE, Sc, Y and Th. In all rare-metal granites, Ta–Nb oxides are characterised by high total REE concentrations and both, negative Eu and Y anomalies in chondrite-normalised REE diagrams.Although constituting a vastly different magmatic system compared to rare metal pegmatites and granites, we included the Upper Fir carbonatite from the Canadian Cordillera, for comparison, because it is characterised by unusal high Ta contents. As expected, the CGM differ from the pegmatitic CGM by having high Mg and Th, and low U concentrations in columbite-(Fe) and lack an Eu anomaly. However, they also show similarities to primitive CGM from rare metal pegmatites of the NYF family in terms of the REE pattern and the increase in #Ta and #Mn towards the margins of the CGM. Our findings support recent results presented in Chudy (2014) indicating that the Ta enrichment in some carbonatites might be attributed to magmatic processes and conditions that are similar to the pegmatitic systems.     

The origin of major talc deposits in the Eastern Desert of Egypt: relict fragments of a metamorphosed carbonate horizon?

Detailed geochemical and mineralogical investigation of four talc deposits in the Eastern Desert of Egypt (Atshan, Abu Gurdi, Darhib and Kashira) suggests that the deposits form a distinct lithological unit within the Shadli metavolcanic rocks. The talc crystallized from the replacement of siliceous carbonate beds locally intercalated with clastic sediments. Th/Yb vs. Ta/Yb ratios of the rocks suggest that the sediments and the host volcanic rocks formed in an active continental margin (ACM) environment. Thus, the talc deposits may represent relict fragments of an ancient, regionally extensive carbonate horizon within the arc-related metavolcanics. The talc-rich rocks, which contain relict carbonate, serpentinized olivine and tremolite, have low (<3 wt%) Al₂O₃, Cr, Ni (<20 ppm), Co and Sc (<15 ppm) concentrations, precluding mafic or felsic igneous protoliths. The deposits were locally affected by contact metamorphism, giving rise to pyroxene-hornfels and granulite facies assemblages, and by regional metamorphism which produced greenschist-amphibolite grade assemblages. Disseminated sulfides commonly occur in the talc-tremolite-rich rocks (having low Al₂O₃ concentrations), suggesting that the metals were probably present in the original carbonate beds, but were remobilized and reconcentrated during the various metamorphic events.