Uranium in supergene phosphorites

The distribution of uranium was studied in supergene phosphorites from the zones of the weathering of sedimentary and endogenous rocks, as well as in nonmarine coprolitic phosphorites and, to a lesser extent, phosphorites from ocean islands. These phosphorites show a diversity of the composition of their carbonate-apatite and structural characteristics. The uranium content ranges mostly from 5 to 100 ppm, with minimum and maximum values of 0.5 and 790 ppm. There is no correlation between the uranium content of a phosphorite and the type of rock with which it is connected. Lacustrine coprolitic phosphorites show elevated uranium contents (about 200 ppm). The maximum uranium content was detected in finely laminated phosphorite encrustations. The correlation analysis of the whole data set (63 samples) showed that uranium content is not correlated with any other component of phosphorites at a confidence level of 0.95. In contrast, there is a correlation between U and P₂O₅, CaO, and F for the combined set of samples from southern Siberian deposits. The significant correlation of U with Na₂O and CO₂ is variable both for southern Siberia on the whole and for particular deposits from this region.     

Signature of potassium enrichment in granite of the Chitrial area, Nalgonda district, Andhra Pradesh: Inferences using its U, Th, K2O, Na2O, Rb, Ba and Sr contents

A medium tonnage unconformity proximal uranium deposit has been established at Chitrial by the Atomic Minerals Directorate in the Srisailam sub-basin. In this type of deposits, the association of uranium with potassic alteration (illitization) is well-documented. The present study is directed towards understanding such an association in the Chitrial area for which the uranium mineralized borehole core samples were collected and analyzed. It is observed that the average concentrations of K₂O, Na₂O, Rb, Ba and Sr in the granite of the Chitrial area are 5.35%, 1.78%, 252 ppm, 564 ppm and 52 ppm, respectively, and they show average critical elemental ratios of K/Rb, Ba/Rb and Rb/Sr as 191, 2.37 and 7.13, respectively. The granites show low K/Rb, low Rb/Ba and high Rb/Sr ratios compared to that of the average crust indicating its derivation from crustal source. The samples have higher values of uranium (av. 53 ppm), thorium (av. 66 ppm) and lead (av. 41 ppm). The U/Th ratio in the granite varies from 0.07 to 20.86 with an average of 1.68. They also exhibit high K₂O/Na₂O ratio typical of post-Archaean granite and very high values suggest the possibility of later potassium enrichment.     

Radioactive quartz-pebble conglomerates from western margin of Bonai granite pluton,Sundargarh district,Orissa — A new find

Several radioactive quartz-pebble conglomerate (QPC) occurrences at the western margin of Archaean Bonai granite and overlying Iron Ore Group (IOG) rocks have recently been located over a total strike length of 8–10 km intermittently in a NE-SW to E-W trend with steep dips due north-west to north in parts of Sundargarh district of Orissa. The QPC samples have analysed up to 0.039% U₃O₈ and 0.035% ThO₂ with high concentration of Y (74 to 518 ppm), La(<100 to 880 ppm), Cr ( 126 to 633 ppm), Zr (137 to 1250 ppm) and Pb (31 to 581 ppm). Cellulose Nitrate (CN) film studies of few QPC samples indicated adsorbed uranium over goethite and infiltrated ferruginous material (limonite), secondary uranium as encrustation and fracture filling and discrete sub-rounded grains of monazite, zircon, allanite and rare xenotime in the matrix of QPC as radioactive phases. Higher content of Th over U, elevated concentration of Y and La in QPC eliminates the possibility of its low temperature product by epigenetic processes. Poor correlation of U with elements like Pb, Y, Zr, La and Cr can be explained due to surficial leaching of uranium from QPC after its deposition as reflected by adsorbed U over iron-oxides and low U/Th ratio in QPC in the area.     

The biogeochemical expression of deeply buried uranium mineralization in Saskatchewan, Canada

Ten kilometres from the eastern edge of the Athabasca Sandstone, near McClean Lake, uranium mineralization (locally up to 27% U₃O₈) lies 150 m beneath the surface at the unconformity between the Athabasca and crystalline basement.A biogeochemical survey of the area sampled A_H and B_F soil horizons, peat moss, and plant organs from the dominant species, viz. black spruce (Picea mariana), jack pine (Pinus banksiana), labrador tea (Ledum groenlandicum), and leather leaf (Chamaedaphne calyculata). Uranium concentrations in the ash of various media are surprisingly high: spruce twigs up to 154 ppm U; labrador tea and leather leaf stems around 100 ppm U. Conversely, labrador tea roots yield < 5 ppm U and spruce trunk wood usually < 1 ppm U. Soils give values of 1–3 ppm U. Contoured U values reveal that highest concentrations occur in plants growing above, but laterally displaced from the mineralization. Track-Etch data show a similar pattern. Upward migration of ions along steeply inclined fractures is invoked to explain the phenomenon. Other elements are present in varying concentrations, depending upon the plant species and the plant organ. High concentrations of several elements are recorded, most notably Cd and Ag in the conifers.     

Occurrence of uranium in metasedimentary enclaves within basement granite, near Peddur and Kottur, Karimnagar District, Andhra Pradesh

Several radioactive anomalies due to uranium and thorium, associated with the mesedimentary enclaves (Archaean) within granite (Archaean to Early-Proterozoic) have been recorded in parts of Karimnagar Granulite Terrain, Karimnagar Dist. At Peddur and Kottur, Uraninite has been identified in the samples of metasediments. The metasediment from these two places have been subjected to granulite facies of metamorphism and host high values of uranium with negligible thorium. In Peddur, samples of metasediments have assayed as high as 1.96% U₃O₈ with negligible thorium, and in Kottur up to 0.059% U₃O₈. Leaching studies on these samples have indicated that most of the U₃O₈ present is leachable. This discovery has opened up the possibility of finding uranium mineralisation in Archaean metasediments and thus provides a thrust for uranium exploration in similar geological environs in India. Further, the basement granite along with the metasedimentary enclaves has the potential to act as a provenance for a possible unconformity type or sandstone type U-deposit in the rocks of overlying Pakhal and Gondwana Supergroup, in Pranhita-Godavari Basin, situated to the east of this area.     

Nature of uranium mineralisation in the Kerpura-Tiwari-ka-bas area,Sikar district,Rajasthan

Mineralisation of uraninite and brannerite occurs in the albitised metasedimentary and intrusive igneous rocks of Kerpura-Tiwari-ka-bas area in Sikar district, Rajasthan. Samples collected from well dumps contain 0.016 to 1.52% U₃O₈ with very low ThO₂. The host rocks show wide variation in chemical composition due to varying degree of alkali metasomatism, associated alteration and composition of protoliths. The spatial distribution of uranium in groundwater as well as rock samples from well dumps indicates localisation of the uranium mineralisation along NNE-SSW and NWSE directions in Kerpura block. Petrographic and lithogeochemical studies point towards close genetic relationship between alkali metasomatism and uranium mineralisation. The mineralisation seems to be due to mobilisation of uranium and other LILEs by metasomatising fluids and their deposition along shear zones at a later stage, which may not be spatially related to zones of intense albitisation.     

Two types of uranium mineralization in Gulcheru quartzite: Fracture-controlled in Ambakapalle area and litho-controlled in Tummalapalle area,Cuddapah Basin,Andhra Pradesh,India

The Cuddapah Basin in southern India has a potential for uranium mineralization due to some favorable factors such as its temporal, stratigraphic and tectonic settings. Systematic exploration program conducted by the Atomic Minerals Directorate for Exploration and Research (AMD) within the Cuddapah Basin resulting in the recognition of distinct types of uranium mineralization, viz., strata bound type, fracture/shear-controlled type and tabular type. The Gulcheru Formation which is the lowermost unit of the Cuddapah Basin is dominantly arenitic in nature. During the exploration works, a number of uranium anomalies were identified with dimensions ranging from 1 m to 1.5 km. Gulcheru quartzite hosted uranium mineralization is intermittent and inconsistent in nature. The anomalous outcrops are distributed over a strike length of ca. 60 km between Gandi in the SE and Ambakapallein the NW. Presently, two different types of uranium mineralization are characterized on the basis of field observations, mapping and structural interpretation, petro-mineralogy and geochemistry. Although the host rock is same for both types, the mechanism of uranium enrichment is totally different. The Ambakapalle uranium mineralization is controlled by fault zone and associated hydrothermal activity. Whereas, the Tummalapalle uranium mineralization is litho-controlled in nature influenced by suitable four ‘P’ factors, i.e., provenance, porosity-permeability, precipitation and preservation. The geochemical characterization of Gulcheru quartzite suggest a passive margin type of provenance setting. Petro-mineralogically the quartz arenite suggests enough textural as well as mineralogical maturity. Ambakapalle quartzite is slightly strained and deformed due to faulting. Analysis of selected samples recorded 0.01% to 0.048% U₃O₈ and <0.01% ThO₂. Petrographic observation revealed that the anomalies were appeared due to secondary uranium minerals occurring as surficial encrustations, fracture filling and lesser irregular patches. Structural analysis suggests the mineralization along E-W trace slip fault is possibly consistent in sub-surface. Tummalapalle quartzite is relatively less deformed arenitic in nature with significant enrichment in MREE. The genetic models for the two types of mineralization is totally different.© 2019 China Geology Editorial Office.     

澳大利亚兰杰一号铀矿之生命周期：地质、资源、生产与修复

兰杰一号铀矿及其所属的鳄鱼河铀矿田产于北澳太古宙克拉通内古元古代裂谷背景下发展起来的松溪造山带,矿体产于新太古代—古元古代结晶-变质基底/晚古元古代—中元古代康博尔吉红层建造不整合界面之下,铀矿化分3个时代,U_1为1720～1680Ma,U_2为1420～1040Ma,U_3为474±6Ma,U1是主矿化时代。该矿床于1969年后期通过航空放射性测量被发现,1970’s经勘探圈定了No.1和No.3两个铀矿体,总计资源储量124681t@0.23%U_3O_8。1980年10月正式露采,至2018年12月,总计生产了128739t U_3O_8。1985财年开始,ERA(澳大利亚能源资源有限责任公司)向世界核能市场共计销售了产于兰杰铀矿的119882t U_3O_8。2009年,发现了No.3深部矿,探明资源储量为43857t@0.22%U_3O_8,这部分资源将以地下开采方式利用。预计到2026年,采区地貌景观和生态环境将得到恢复。进一步讨论了澳北元古宙不整合面型铀矿找矿的方向,持续稳定的铀矿开采与生产的意义,以及投资澳大利亚铀矿业需要注意的政治与法律问题。这些内容可以为国内矿业企业及地勘单位合理部署澳洲铀矿勘查与开发提供参考。     

On “Birthmarks” in rare-metal granites of the Losevka pluton,northern Kazakhstan

The Losevka pluton of rare-metal albite granite, which was explored as a possible source of columbite-zircon-malacon ore, is composed of quartz, sodic plagioclase, potassium feldspar, annite, protolithionite, lepidomelane, and Li-muscovite. The average chemical composition of this rock is as follows, wt %: 74.14 SiO₂, 0.04 TiO₂, 14.07 Al₂O₃, 1.05 Fe₂O₃, 0.78 FeO, 0.15 MnO, 0.09 MgO, 0.47 CaO, 4.65 Na₂O, 4.11 K₂O, and 0.03 P₂O₅. The accessory minerals are zircon, malacon, and cyrtolite (874 ppm); apatite (18 ppm); ilmenite (114 ppm); xenotime and monazite (119 ppm); and Nb-columbite (463 ppm). The black inclusions up to 15 cm in size, which are observed in this granite and called “birthmarks” by local geologists, consist of the same rock-forming minerals as the surrounding granite, but are enriched in MnO, MgO, CaO, TiO₂, and F and depleted in SiO₂ relative to the light granite. The black granite is also distinguished by much higher Sr and Ba contents and lower La, Rb, Y, Nb, REE, Cs, Ta, Th, and U contents. The black color is caused by enrichment in manganese oxides, manganoilmenite, and Mn-annite. All rock-forming minerals are pervaded by thin veinlets of Mn-oxides. In addition, bastnaesite, Y-and Th-fluorides, zircon, and malacon have been identified. Aggregates of black-colored minerals are not the products of the fractionation of the initial magma or immiscibility effects, because the structure of the albite-potassium feldspar-quartz-mica matrix is the same both in black and light granites. The percolation of a deep-sourced fluid enriched in Mn and F into a granitic melt might be a more probable origin.     

Unique accessory Ti-Ba-P mineralization in the Kvalöya ultrapotassic dike,Northern Norway

Unusual ultrapotassic dikes were recently found on the Kvalöya Island in Northern Norway. The dikes crosscutting granites 1.8 Ga in age are 0.1–1.0 m thick and consist of phlogopite phenocrysts in a fine-grained groundmass of K-magnesioarfvedsonite, orthoclase, apatite, and secondary chlorite. According to the composition of the rock-forming minerals (4.5–6.0 wt % K₂O and 0.7–3.5 wt % TiO₂ in magnesioarfved-sonite, 1.6–3.6 wt % FeO in orthoclase, 9.2–10.7 wt % Al₂O₃ and 2.1–2.6 wt % TiO₂ in phlogopite) and its bulk chemical composition (K/Na = 2.3–2.9, K/Al = 1.0–1.2, (Na + K)/Al = 1.4–1.7, Mg# V = 65–73, (La/Yb) _n = 100–140, 3.2–4.0 wt % TiO₂, 0.55–1.47 wt % BaO, 2.5–3.0 wt % P₂O₅, 2650–3000 ppm Zr, 900–1260 ppm REE total, 2300–2500 ppm Sr), the rock corresponds to lamproite of the transitional type. The unique chemical composition of the rock resulted in uncommon Ti-Ba-P accessory mineralization, including baotite Ba₄(Ti,Nb)₈Si₄O₂₈Cl (up to 5 vol %), Sr-apatite (5–7 vol %), and previously unknown Na-Mg-Ba phosphate. Baotite forms anhedral elongated and isometric grains 10–500 μm in size. It is characterized by low Nb (0.03–0.05 f.c.); admixtures of K (0.04–0.12 f.c.) and Sr (0.04–0.07) replacing Ba and Fe (0.01–0.03 f.c.); and Al (0.03–0.04 f.c.) substituting Ti. Euhedral elongated zonal apatite crystals are extremely enriched in SrO (8–12 wt %) and REE₂O₃ + Y₂O₃ (6–9 wt %) in the marginal zone. Na-Mg-Ba phosphate occurs as prismatic grains 10–100 μm in size. The atomic ratio of its major cations Na: Mg: Ba: P ～ 2: 1: 1: 2 corresponds to the conventional formula Na₂MgBa(PO4)2; the mineral contains Sr, Mn, Fe, Ca, Si, and Al admixtures.     

Radioelement Mapping and Environmental Monitoring of Surface Deposits using Ground Gamma Ray Spectrometry of the Area Adjacent to El‐Ramlah Village,Southwestern Sinai,Egypt

A ground‐based gamma‐ray survey has been performed in the area close to El‐Ramlah village, southwestern Sinai, Egypt, using a GS‐512 spectrometer. The main objective of this survey was to delineate radioactive anomalies within the surface of the study area and to identify the environmental effects of natural radioelements on the new inhabitants, Bedouins, who live in the recently built village in this region of the Sinai Peninsula. The results show that the maximum radioactivity of the total count component (T.C.) was about 15.7Ur at the northern part of the study area. The average radioelements concentration were 0.4% for potassium, 1.6 ppm for equivalent uranium and 4.5 ppm for equivalent thorium. To identify and map the environmental effects of the concentration of these radioelements on El‐Ramlah village, measurements of potassium (K%), equivalent uranium (eU) and equivalent thorium (eTh) were converted into an equivalent dose rate. The results illustrate that, the levels of effective dose rate of the natural radioactivity of the area of study remains in the safe range without any harm to living organisms, and it stays within the maximum permissible radiation dose rate (1.0 mSv y^?1) recommended by the International Commission of Radiological Protection.     

Evidence of uranium biomineralization in sandstone-hosted roll-front uranium deposits, northwestern China

We show evidence that the primary uranium minerals, uraninite and coffinite, from high-grade ore samples (U₃O₈>0.3%) in the Wuyiyi, Wuyier, and Wuyisan sandstone-hosted roll-front uranium deposits, Xinjiang, northwestern China were biogenically precipitated and psuedomorphically replace fungi and bacteria. Uranium (VI), which was the sole electron acceptor, was likely to have been enzymically reduced. Post-mortem accumulation of uranium may have also occurred through physio-chemical interaction between uranium and negatively-charged cellular sites, and inorganic adsorption or precipitation reactions. These results suggest that microorganisms may have played a key role in formation of the sandstone- or roll-type uranium deposits, which are among the most economically significant uranium deposits in the world.     

Whole-rock chemistry of the Gameleira I uranium deposit,Lagoa Real,Brazil

The Lagoa Real uranium (U) province, referred to as Lagoa Real, is located in the state of Bahia, north-eastern Brazil. Lagoa Real has ∼112,000 metric tonnes and average grade of 2700 ppm of U₃O₈, being one of the largest U deposits in the world and the largest in Brazil. Despite its economic and strategic importance, there are gaps in the geological knowledge of the Lagoa Real U deposits. One of them is the lack of extensive whole-rock chemical data sets. Here, we present whole-rock chemical analyses for major and trace elements, including the rare-earth elements (REE), from barren country rocks to uraniferous ore shoot, systematically sampled from an exploratory drill hole. The chemical data indicate that albitite rocks, with and without uraniferous mineralisation, cannot result from sodic syenitic magmatism, as proposed by recent studies. Petrographical and geochemical evidence supports the previously suggested concept that the Lagoa Real albitite rocks resulted from sodic metasomatism of the granitic country rock, known as the São Timóteo granite. Their ore-mineral assemblages and geochemical characteristics are similar to albitite-hosted U deposits worldwide.     

Petrography and geochemistry of uranium mineralised Precambrian granitic-pegmatitic rocks of Mawlait, West Khasi Hills district, Meghalaya

During radiometric investigation at Mawlait, significant uranium mineralisation (0.024–0.22%U₃O₈) was located mainly within the small pegmatite (garnet bearing quartzofeldspathic rock), which are locally segregated within migmatite at Umiang River section. Pink granite and granite gneisses are the dominant lithounits of the study area showing fertile character and spotty radioactivity at several places. Radioactivity in these rocks is mainly contributed by discrete uraninite grains along with some zircon and xenotime. Granites are peraluminous, low-Ca in nature and their geochemical signatures suggest derivation from a felsic source. Discriminant diagrams using Rb, Nb and Y indicate ‘within plate’ to ‘volcanic arc’ nature of the rock. The uraniferous pegmatitic veins within migmatite appear to have formed due to localised metamorphic segregation during late stage of anatexis. Petromineralogical and geochemical studies suggest that the uranium mineralisation in granitic-pegmatitic rocks of the area is mainly syn-magmatic type.     

Uranium anomalies in paleo-aquifers near sandstone-type uranium deposits in the devonian catskill formation of Pennsylvania

Background values of U and Th in 371 clastic sedimentary rocks from the Catskill Formation correlate negatively with Si and positively with Al and most other major elements because of the low content of U and Th in quartz and the relative enrichment in clays, Fe oxides, and other fine-grained components. Background U also correlates closely with Th. Similar results are obtained from 100 samples from western Colorado near the Uravan mineral belt. Weak anomalies in U are much more easily recognized by study of residuals or deviations from regressions of U against Al or Th than in the raw data.At Penn Haven Junction near Jim Thorpe, Pa., roll-type uranium deposits similar to those in Wyoming are localized around an iron-stained paleo-aquifer of conglomeratic sandstone. Twenty-four rock samples from this paleo-aquifer contain 1–12 ppm U; eight of the samples contain less than 4 ppm U, the background level for shales of the area. Uranium residuals from regressions against Al or Th are clearly anomalous for all samples. Experiments on another group of samples suggest that readily extractable U (H₂O₂-acetic acid leach) would also show the paleo-aquifer to be anomalous.Anomalies of this type in paleo-aquifers should be useful in evaluation of drill holes, outcrops, and radiometric data in prospective districts, especially when paleo-aquifers are difficult to recognize visually. The anomalies also indicate that U is added to sandstones of the paleo-aquifer rather than leached out to form the ore bodies in reduced rocks at the margins of a geochemical cell.     

Geochemistry of Proterozoic Radioactive Arkoses in Khammam District,Andhra Pradesh,India: Evidence for K-rich Evolved Granitoid Upper Crust in the Late Archaean

Geochemical studies on radioactive arkoses (43–153 ppm U and 387–862 ppm Th) of the Proterozoic Pakhal Supergroup from Bangaruchilka, Khammam district, Andhra Pradesh, India, indicate that their gross major and trace element chemistry reflect their mineral composition. Chemically, arkoses are rich in silica (83% to 88% SiO₂) and potassium (3% to 5% K₂O), with consistently high Al₂O₃/Na₂O (36 to 50) and K₂O/Na₂O (18 to 25) ratios, which indicate that they are chemically mature sediments. The arkoses also show higher concentrations of Ti, V, Cr, Ni, Cu, Y, Zr, Nb, La and Pb.The values (60% to 68%) of chemical alteration index (CIA) of studied arkoses are moderate, and indicate that the source rocks have undergone lesser degree of chemical weathering. Tectonic setting discriminate plots of Fe₂O₃ (total)/MgO vs. TiO₂ and Al₂O₃/SiO₂, and K₂O/Na₂O vs. SiO₂ and SiO₂/Al₂O₃ indicate that the Bangaruchilka arkoses represent the sediments that were deposited in passive continental margin (PM), which is further supported by association of platformal type of sediments (quartzites and phyllites) with them. Unlike middle Archaean sedimentary rocks, the studied arkoses are depleted in Na₂O, MgO and CaO, and distinctly enriched in SiO₂ and K₂O. These geochemical features match with post-Archaean clastic sediments, which argues for the involvement of late Archaean granitic crust in supply of detritus of studied arkoses. Enrichment of potassium alongwith abundant microcline and elevated concentrations of Y, Zr, Nb, U, Th, La, etc. in arkoses indicate K-rich evolved granitoid upper crust in the provenance during the late Archaean-early Proterozoic period.Dominance of mechanical weathering over chemical weathering favoured arkose formation, and also transfer of radio-elements with clastic sediments into the Pakhal basin. After sedimentation, uranium seems to have been remobilised from the rocks of Archaean-Pakhal system, consequent to post-sedimentation structural disruptions, and concentrated along suitable structural loci. Therefore, it is likely to encounter significant concentration of uranium in close proximity of unconformable Archaean and Pakhal contacts and tectonic zones, thereby making Pakhal basin and its environs a suitable terrain to search for concealed uranium mineralisation.     

Geochemical behaviour of LREE,Y and Zr in uranium mineralized and non-mineralized granite from Darshanapur area,in the Gogi-Kurlagere fault zone,Bhima basin,Yadgiri district,Karnataka

Granite core samples (n=14) from the Gogi-Kurlagere fault zone in the central part of the Bhima basin were studied in terms of LREE, Y and Zr mobility during uranium mineralization. LREE, Zr and Y along with LILE (Ba, Rb) and P show behavioral differences in the mineralised and the non-mineralised samples. Average ΣLREE in mineralised granite (240 ppm) is higher than in non-mineralised samples (157 ppm). The average Zr and Y in the mineralised granite are 193 ppm and 17 ppm, while the corresponding abundances of these elements in non-mineralised portion are 148 ppm and 11 ppm respectively. Besides enrichment of U, Th, Ba, Pb and Rb and depletion of Sr are observed in mineralized granite in comparison to non-mineralized granite. Hydrothermal alteration has led to the mobility of these elements, which again dependent on the overall geochemical behavior of the migrating fluid. REE and Y in association with uranyl [(UO₂)²⁺] ion were transported as carbonate complexes like [UO₂(CO₃)₃]^4- and [REE (CO₃)₃]^3- and were later incorporated into favourable structural loci by precipitating minerals like pitchblende and coffinite.     

Occurrence of Li,B, Cu and Zn in some Egyptian Nile sediments

Lithium, boron, copper and zinc have been determined on cored and surface sediments from the delta and the drainage valley of the Nile River. The clay size fraction separated from the samples consists of montmorillonite and kaolinite as the predominant clay components, followed by illite and chlorite. Quartz and calcite are the non-clay admixtures.Lithium content varies between 7 and 48 ppm in the bulk sediments and between 28 and 61 ppm in the clay fractions, being clearly enriched in the clay material. In the clay fractions, concentration of lithium in kaolinite is indicated by a close relation between the lithium and kaolinite contents and is further supported by a close correlation with A1₂O₃.Boron in the clay fraction (62–112 ppm) appears to be concentrated in detrital illite.The concentrations of copper (26–900 ppm) and zinc (65–333 ppm) in the clay fractions correlate positively with the CO₂ percentage. Both elements tend to occur in or on the claysized grains of caleite.     

The abundance and distribution of uranium in some oceanic,continental ultramafic inclusions and host basalts

The abundance and distribution of uranium in various continental and oceanic ultramafic inclusions and host basalts are reported. Uranium was determined by neutron activation (fission products, fission tracks and delayed-neutron methods) and alpha-particle autoradiography; data is also reported for the uranium content of various USGS standard rock powders. The concentration of uranium in both oceanic and continental samples is similar, levels are controlled by mineral compositions, and their relative abundance in different rock types. Highest levels are found in feldspathic and lowest in olivine rich inclusions. Uranium is enriched in mylonitised samples and along some inter-crystal boundaries. With the exception of some apatites, highest levels of uranium are in clinopyroxenes (chrome) and lowest in olivines; no enrichment of uranium in orthopyroxenes was observed. Attention is drawn to the problem of obtaining representative samples from the sea floor which have not been altered by saline solutions and the identification of uranium and daughter products present along inter-crystal boundaries. Differences in observed heat flow between continental and oceanic areas may reflect inadequate sampling of representative rock types present below the sea floor and lack of information for the true abundance and distribution of uranium in such rocks.     

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.