Sample records for wolframite

  1. Wolframite Conversion in Treating a Mixed Wolframite-Scheelite Concentrate by Sulfuric Acid

    NASA Astrophysics Data System (ADS)

    Shen, Leiting; Li, Xiaobin; Zhou, Qiusheng; Peng, Zhihong; Liu, Guihua; Qi, Tiangui; Taskinen, Pekka

    2017-12-01

    Complete wolframite conversion in sulfuric acid is significant for expanding the applicability of the sulfuric acid method for producing ammonium paratungstate. In this paper, the conversion of wolframite in treating a mixed wolframite-scheelite concentrate by sulfuric acid was studied systematically. The results show that the conversion of wolframite in sulfuric acid is more difficult than that of scheelite, requiring rigorous reaction conditions. A solid H2WO4 layer forms on the surfaces of the wolframite particles and becomes denser with increasing H2SO4 concentration, thus hindering the conversion. Furthermore, the difficulty in wolframite conversion can be mainly attributed to the accumulation of Fe2+ (and/or Mn2+) in the H2SO4 solution, which can be solved by reducing Fe2+ (and/or Mn2+) concentration through oxidization and/or a two-stage process. Additionally, the solid converted product of the mixed wolframite-scheelite concentrate has an excellent leachability of tungsten in an aqueous ammonium carbonate solution at ambient temperature, with approximately 99% WO3 recovery. This work presents a route for manufacturing ammonium paratungstate by treating the mixed concentrate in sulfuric acid followed by leaching in ammonium carbonate solution.

  2. Wolframite Conversion in Treating a Mixed Wolframite-Scheelite Concentrate by Sulfuric Acid

    NASA Astrophysics Data System (ADS)

    Shen, Leiting; Li, Xiaobin; Zhou, Qiusheng; Peng, Zhihong; Liu, Guihua; Qi, Tiangui; Taskinen, Pekka

    2018-02-01

    Complete wolframite conversion in sulfuric acid is significant for expanding the applicability of the sulfuric acid method for producing ammonium paratungstate. In this paper, the conversion of wolframite in treating a mixed wolframite-scheelite concentrate by sulfuric acid was studied systematically. The results show that the conversion of wolframite in sulfuric acid is more difficult than that of scheelite, requiring rigorous reaction conditions. A solid H2WO4 layer forms on the surfaces of the wolframite particles and becomes denser with increasing H2SO4 concentration, thus hindering the conversion. Furthermore, the difficulty in wolframite conversion can be mainly attributed to the accumulation of Fe2+ (and/or Mn2+) in the H2SO4 solution, which can be solved by reducing Fe2+ (and/or Mn2+) concentration through oxidization and/or a two-stage process. Additionally, the solid converted product of the mixed wolframite-scheelite concentrate has an excellent leachability of tungsten in an aqueous ammonium carbonate solution at ambient temperature, with approximately 99% WO3 recovery. This work presents a route for manufacturing ammonium paratungstate by treating the mixed concentrate in sulfuric acid followed by leaching in ammonium carbonate solution.

  3. Fertility of Rare-Metal Peraluminous Granites and Formation Conditions of Tungsten Deposits

    NASA Astrophysics Data System (ADS)

    Syritso, L. F.; Badanina, E. V.; Abushkevich, V. S.; Volkova, E. V.; Terekhov, A. V.

    2018-01-01

    The tungsten distribution in rocks of the Kukulbei Complex in eastern Transbaikal region results in a high potential of rare-metal peraluminous granites (RPG) for W mineralization and displays a different behavior of W in Li-F and "standard" RPG. These subtypes differ in the behavior of W in melt, spatial localization of mineralization, and the timing of wolframite crystallization relative to the age of the parental granitic rocks. The significant of W concentration is assumed to be due to fractionation of the Li-F melt; however, wolframite mineralization in Li-F enriched granite is not typical in nature. The results of experiments and our calculations of W solubility in granitic melt show that wolframite hardly ever crystallizes directly from melt; it likely migrates in the fluid phase and is then removes from the magma chamber to the host rocks, where secondary concentration takes place in exocontact greisens and quartz-cassiterite-wolframite veins. At the same time, the isotopic age of accessory wolframite (139.5 ± 2.1 Ma) within the Orlovka massif of Li-F granite is close to the formation age of the massif (140.6 ± 2.9 Ma). A different W behavior is recorded in the RPG subtype with a low lithium and fluorine concentration, exemplified by the Spokoininsky massif. There is no significant W gain in the melt. All varieties of wolframite mineralization in the Spokoininsky massif are derived from greisens, veins, and pegmatoids yielding the same crystallization ages (139.5 ± 1.1 Ma), which are 0.9-1.8 Ma later (taking into account the mean-square weighted deviation) than the Spokoininsky granite formation (144.5 ± 1.4 Ma). Perhaps this period corresponds to the time of transition from the magmatic stage to hydrothermal alteration. Comparison of the isotope characteristics (Rb-Sr and Sm-Nd isotope systems) of rocks and the associated ore minerals (wolframite, cassiterite) from all examined deposits shows a depletion in ɛNd values for ore minerals relative to the rock and the opposite behavior for the intial Sr isotope ratios. This may indicate the specific nature of ore matter, where the effect of the juvenile component is definitely expressed. Our geochronological results show that tantalum and tungsten mineralization took place within a narrow age interval, almost synchronously with the crystallization of associated granites. The coeval development of peraluminous magmatism enriched in lithophile rare elements and volatiles with ore complexes located in different structural settings and separated by a considerable distance from each other (up to 500 km) suggests a regional and deep-seated magma source. Rifting and increased thermal flux from the mantle, manifestations of which have been recorded during this period in the territory, may be a deep-seated process.

  4. 40 Ma of hydrothermal W mineralization during the Variscan orogenic evolution of the French Massif Central revealed by U-Pb dating of wolframite

    NASA Astrophysics Data System (ADS)

    Harlaux, Matthieu; Romer, Rolf L.; Mercadier, Julien; Morlot, Christophe; Marignac, Christian; Cuney, Michel

    2018-01-01

    We present U-Pb thermal ionization mass spectrometer (TIMS) ages of wolframite from several granite-related hydrothermal W±Sn deposits in the French Massif Central (FMC) located in the internal zone of the Variscan belt. The studied wolframite samples are characterized by variable U and Pb contents (typically <10 ppm) and show significant variations in their radiogenic Pb isotopic compositions. The obtained U-Pb ages define three distinct geochronological groups related to three contrasting geodynamic settings: (i) Visean to Namurian mineralization (333-327 Ma) coeval with syn-orogenic compression and emplacement of large peraluminous leucogranites (ca. 335-325 Ma), (ii) Namurian to Westphalian mineralization (317-315 Ma) synchronous with the onset of late-orogenic extension and emplacement of syn-tectonic granites (ca. 315-310 Ma) and (iii) Stephanian to Permian mineralization (298-274 Ma) formed during post-orogenic extension contemporaneous with the Permian volcanism in the entire Variscan belt. The youngest ages (276-274 Ma) likely reflect the reopening of the U-Pb isotopic system after wolframite crystallization and may correspond to late hydrothermal alteration (e.g. ferberitization). Our results demonstrate that W(±Sn) mineralization in the FMC formed during at least three distinct hydrothermal events in different tectono-metamorphic settings over a time range of 40 Ma.

  5. Analytical Fingerprint of Wolframite Ore Concentrates.

    PubMed

    Gäbler, Hans-Eike; Schink, Wilhelm; Goldmann, Simon; Bahr, Andreas; Gawronski, Timo

    2017-07-01

    Ongoing violent conflicts in Central Africa are fueled by illegal mining and trading of tantalum, tin, and tungsten ores. The credibility of document-based traceability systems can be improved by an analytical fingerprint applied as an independent method to confirm or doubt the documented origin of ore minerals. Wolframite (Fe,Mn)WO 4 is the most important ore mineral for tungsten and is subject to artisanal mining in Central Africa. Element concentrations of wolframite grains analyzed by laser ablation-inductively coupled plasma-mass spectrometry are used to establish the analytical fingerprint. The data from ore concentrate samples are multivariate, not normal or log-normal distributed. The samples cannot be regarded as representative aliquots of a population. Based on the Kolmogorov-Smirnov distance, a measure of similarity between a sample in question and reference samples from a database is determined. A decision criterion is deduced to recognize samples which do not originate from the declared mine site. © 2017 American Academy of Forensic Sciences.

  6. Tungsten resources of Brazil

    USGS Publications Warehouse

    White, Max Gregg

    1974-01-01

    Brazilian tungsten production, 85 percent of which is exported, comes almost entirely from scheelite-bearing tactites in northeast Brazil, and has reached an annual rate of about 2,000 metric tons (2,200 short tons) of scheelite concentrate with 70 percent WO3. Scheelite ore reserves, located principally in the State of Rio Grande do Norte, are estimated to be as high as 8,300,000 tons (9,100,000 short tons) containing 0.7 percent WO3. Minor deposits (or those about which only minimal information is available) of wolframite, with which some cassiterite is associated, are located in Sao Paulo, Santa Catarina, and Rio Grande do Sul. Both the scheelite and the wolframite deposits are considered . to be late Precambrian A (620 to 900 m.y.) or early Cambrian in age.

  7. Role of the chemical substitution on the luminescence properties of solid solutions Ca{sub (1−x)}Cd{sub (x)}WO{sub 4} (0 ≤ x ≤1)

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Taoufyq, A.; Laboratoire Matériaux et Environnement LME, Faculté des Sciences, Université Ibn Zohr, BP 8106, Cité Dakhla, Agadir; CEA, DEN, Département d'Etudes des Réacteurs, Service de Physique Expérimentale, Laboratoire Dosimétrie Capteurs Instrumentation, 13108 Saint-Paul-lez-Durance

    2015-10-15

    Highlights: • Luminescence can be modified by chemical substitution in solid solutions Ca{sub 1−x}Cd{sub x}WO{sub 4}. • The various emission spectra (charge transfer) were obtained under X-ray excitation. • Scheelite or wolframite solid solutions presented two types of emission spectra. • A luminescence component depended on cadmium substitution in each solid solution. • A component was only characteristic of oxyanion symmetry in each solid solution. - Abstract: We have investigated the chemical substitution effects on the luminescence properties under X-ray excitation of the solid solutions Ca{sub (1−x)}Cd{sub (x)}WO{sub 4} with 0 ≤ x ≤ 1. Two types of wide spectralmore » bands, associated with scheelite-type or wolframite-type solid solutions, have been observed at room temperature. We decomposed each spectral band into several spectral components characterized by energies and intensities varying with composition x. One Gaussian component was characterized by an energy decreasing regularly with the composition x, while the other Gaussian component was only related to the tetrahedral or octahedral configurations of tungstate groups WO{sub 4}{sup 2−} or WO{sub 6}{sup 6−}. The luminescence intensities exhibited minimum values in the composition range x < 0.5 corresponding to scheelite-type structures, then, they regularly increased for cadmium compositions x > 0.5 corresponding to wolframite-type structures.« less

  8. New Insights into the Role of Pb-BHA Complexes in the Flotation of Tungsten Minerals

    NASA Astrophysics Data System (ADS)

    Yue, Tong; Han, Haisheng; Hu, Yuehua; Sun, Wei; Li, Xiaodong; Liu, Runqing; Gao, Zhiyong; Wang, Li; Chen, Pan; Zhang, Chenyang; Tian, Mengjie

    2017-11-01

    Lead ions (lead nitrate) were introduced to modify the surface properties of tungsten minerals, effectively improving the floatability, with benzohydroxamic acid (BHA) serving as the collector. Flotation tests indicated that Pb-BHA complexes were the active species responsible for flotation of the tungsten minerals. The developed Pb-BHA complexes and the novel flotation process effectively increased the recovery of scheelite and wolframite, simplified the technological process, and led to reduced costs. Fourier transform infrared spectra data showed the presence of adsorbed Pb-BHA complexes on the surface of the minerals. The characteristic peaks of BHA shifted by a considerable extent, indicating that chemical adsorption plays an important role in the flotation process. Zeta potential results confirmed physical adsorption of the positively charged Pb-BHA complexes on the mineral surfaces. The synergistic effect between chemical and physical adsorption facilitated the maximum flotation recovery of scheelite and wolframite.

  9. Petrogenesis of the Bosworgey granitic cusp in the SW England tin province and its implications for ore mineral genesis

    NASA Astrophysics Data System (ADS)

    Ball, T. K.; Basham, I. R.

    1984-01-01

    The Bosworgey granite cusp forms an apical portion of the concealed northern extension of the Tregonning-Godolphin granite ridge. It is characterised by unusually high values of B, P, Mn, Fe, As, Cu, Nb, Ta, Bi, Sn, W, U and S which are present largely as tourmaline, apatite, pyrite, arsenopyrite, chalcopyrite, bismuth, columbite, cassiterite, wolframite and uraninite; and low levels of Zr, Hf, Ti and REE present in zircon, ilmenite and monazite. The granite is classified as Sn and W “specialised” (Tischendorf, 1974) and it belongs to the ilmenite series of Japanese workers. The classification of Chappell and White (1974) (“S” and “I” type granites) is shown to be inapplicable to Cornubian rocks although the Bosworgey samples show characteristics of “S” type granites. The accessory mineral assemblages are typical of high temperature lodes (cassiterite, wolframite, arsenopyrite, chalcopyrite) and the assamblage is concluded to be the cusp analogue of hypothermal lodes produced by extreme differentiation and concentration of volatiles. It is speculated that such granites could provide the parent material for the mesothermal crosscourse mineralisation (pitchblende, bismuth, pyrite, galena, sphalerite).

  10. The Black Pearl mine, Arizona - Wolframite veins and stockscheider pegmatite related to an albitic stock

    NASA Technical Reports Server (NTRS)

    Schmitz, Christopher; Burt, Donald M.

    1990-01-01

    Wolframite-bearing quartz veins flanked by greisen alteration occur at and near the Black Pearl mine, Yavapai County, Arizona. The veins are genetically related to a small albitite stock, and cut a series of Proterozoic metasedimentary and intrusive rocks. The largest vein, the only one mined, is located at the apex of the stock. Field relations imply that this stock is a late-stage differentiate of time 1.4-Ga anorogenic Lawler Peak batholith, which crops out about 3 km to the south. The albitites are of igneous origin and have suffered only minor deuteric alteration. A thin (1 to 2 m) pegmatite unit ('stockscheider') occurs at the contact of the Black Pearl Albitite stock with the country rocks. Directional indicators and other evidence suggest that the pegmatite was formed in the presence of a volatile-rich fluid phase close to the time of magma emplacement. The sudden change from coarse-grained microcline-rich pegmatite to fine-grained, albite-rich albitite suggests pressure quenching, possibly due to escape of fluids up the Black Pearl vein. Stockscheider-like textures typically occur near the apical contacts of productive plutons. The presence or absence of this texture is a useful guide in prospecting for lithophile metal deposits.

  11. Mineral resource of the month: tungsten

    USGS Publications Warehouse

    Shedd, Kim B.

    2012-01-01

    The article offers information on tungsten. It says that tungsten is a metal found in chemical compounds such as in the scheelite and ore minerals wolframite. It states that tungsten has the highest melting point and it forms a compound as hard as diamond when combined with carbon. It states that tungsten can be used as a substitute for lead in fishing weights, ammunition, and hunting shot. Moreover, China started to export tungsten materials and products instead of tungsten raw materials.

  12. DOE Office of Scientific and Technical Information (OSTI.GOV)

    Carnahan, T.G.; Kazonich, G.; Raddatz, A.E.

    The U.S. Bureau of Mines conducted a bench-scale study to delineate the important parameters in a three-step process to produce commercial-quality tungsten carbide (WC) directly from tungsten minerals. In the process, tungsten concentrates of wolframite or wolframite and scheelite are decomposed at 1,050{sup 0}C in a molten mixture of NcCl and Na{sub 2}SiO{sub 3} that forms two immiscible phases. Tungsten, as sodium tungstate, reports to the halide phase and is separated from the gangue constituents, which report to the silicate phase. After decanting to separate the two phases, natural gas is sparged into the molten halide phase a 1,070{sup 0}C.more » Submicrometer crystals of WC are initially produced. These crystals grow into thin triangular-shaped plates up to 100 {mu}m on a side or into popcorn-shaped conglomerates. Sparged WC was examined for its suitability for use in sintered carbide products. In physical evaluations, sparged WC ground to an average particle size of 1.52 {mu}m and compacted with 10 pct Co binder into standard 6-by 22-mm test bars had a density of 14.35 and a Rockwell A hardness of 89.6. This compared favorably with 14.39 and 89.7 respectively, for test bars made from a standard commercial 1.52-{mu}m WC powder. Test bars made from Bureau of Mines WC had no C'' porosity or eta phase.« less

  13. Fluid inclusion characteristics and geological significance of the Dajinshan W-Sn polymetallic deposit in Yunfu, Guangdong Province

    NASA Astrophysics Data System (ADS)

    Yu, Zhangfa; Chen, Maohong; Zhao, Haijie

    2015-05-01

    The Dajinshan tungsten-tin polymetallic deposit is a quartz-vein-type ore deposit located in Western Guangdong Province. The ore bodies show a fairly simple shape and mainly occur as tungsten-tin polymetallic-bearing sulfide quartz veins, including quartz vein, quartz-greisens, and sulfide quartz veins, and their distribution is spatially related to Dajinshan granitoids. The formation of the deposit experienced three stages: a wolframite-molybdenite-quartz stage, a wolframite-cassiterite-sulfide-quartz stage, and a fluorite-calcite-carbonate stage. Based on detailed petrographic observations, we conducted microthermometric and Raman microspectroscopic studies of fluid inclusions formed at different ore-forming stages in the Dajinshan tungsten-tin polymetallic deposit, identifying four dominant types of fluid inclusions: aqueous two-phase inclusions, CO2-bearing inclusions, solid or daughter mineral-bearing inclusions, and gas-rich inclusions. The gas compositions of ore-forming fluids in the Dajinshan tungsten-tin polymetallic deposit are mostly CO2, CH4, and H2O. The hydrogen, oxygen, and sulfur isotopic data imply that the ore-forming fluids in the Dajinshan tungsten-tin polymetallic deposit were mainly derived from magmatic fluids, mixed with meteoric water in the ore-formation process. These results indicate that the fluid mixing and boiling led to the decomposition of the metal complex in ore-forming fluids and ore deposition.

  14. Structural, vibrational and luminescence properties of the (1−x)CaWO{sub 4}−xCdWO{sub 4} system

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Taoufyq, A.; Laboratoire Matériaux et Environnement LME, Faculté des Sciences, Université Ibn Zohr, BP 8106, Cité Dakhla, Agadir, Maroc; CEA/DEN, Département d’Études des Réacteurs, Laboratoire Dosimétrie Capteurs Instrumentation, CEA Cadarache, 13108, Saint-Paul-lez-Durance

    2014-11-15

    In the present work, we investigate the structural, microstructural, vibrational and luminescence properties of the system (1−x)CaWO{sub 4}−xCdWO{sub 4} with x ranging between 0 and 1. Polycrystalline samples were elaborated using a coprecipitation technique followed by thermal treatment at 1000 °C. The samples were then characterized using X-ray diffraction, scanning electron microscopy, Raman spectroscopy and luminescence analyses. X-ray diffraction profile analyses using Rietveld method showed that two kinds of solid solutions Ca{sub 1−x}Cd{sub x}WO{sub 4} having scheelite and wolframite structures, with respectively tetragonal and monoclinic crystal cells, were observed, with a biphasic system for compositions x=0.6 and 0.7. The scanningmore » electron microscopy experiments showed a complex evolution of morphologies and crystallite sizes as x increased. The vibration modes of Raman spectra were characteristic of composition-dependent disordered solid solutions with decreasing wavenumbers as x increased. Luminescence experiments were performed under UV-laser light irradiation. The energies of emission bands increased linearly with cadmium composition x. The integrated intensity of luminescence reached a maximum value for the substituted wolframite phase with composition x=0.8. - Graphical abstract: Luminescence on UV excitation (364.5 nm) of (1−x)CaWO{sub 4−x}CdWO{sub 4} system, elaborated from coprecipitation technique at 1000 °C, with 0« less

  15. PHASE EVOLUTION AND MICROWAVE DIELECTRIC PROPERTIES OF (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) CERAMICS WITH ULTRA-LOW SINTERING TEMPERATURES

    NASA Astrophysics Data System (ADS)

    Zhou, Di; Guo, Jing; Yao, Xi; Pang, Li-Xia; Qi, Ze-Ming; Shao, Tao

    2012-11-01

    The (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) ceramics were prepared via the solid state reaction method. The sintering temperature decreased almost linearly from 755°C for (Li0.5Bi0.5)WO4 to 560°C for (Li0.5Bi0.5)MoO4. When the x≤0.3, a wolframite solid solution can be formed. For x = 0.4 and x = 0.6 compositions, both the wolframite and scheelite phases can be formed from the X-ray diffraction analysis, while two different kinds of grains can be revealed from the scanning electron microscopy and energy-dispersive X-ray spectrometer results. High performance of microwave dielectric properties were obtained in the (Li0.5Bi0.5)(W0.6Mo0.4)O4 ceramic sintered at 620°C with a relative permittivity of 31.5, a Qf value of 8500 GHz (at 8.2 GHz), and a temperature coefficient value of +20 ppm/°C. Complex dielectric spectra of pure (Li0.5Bi0.5)WO4 ceramic gained from the infrared spectra were extrapolated down to microwave range, and they were in good agreement with the measured values. The (Li0.5Bi0.5)(W1-xMox)O4(0.0 ≤ x ≤ 1.0) ceramics might be promising for low temperature co-fired ceramic technology.

  16. Fluid evolution and ore genesis of the Dalingshang deposit, Dahutang W-Cu ore field, northern Jiangxi Province, South China

    NASA Astrophysics Data System (ADS)

    Peng, Ning-Jun; Jiang, Shao-Yong; Xiong, Suo-Fei; Pi, Dao-Hui

    2018-02-01

    The Dalingshang W-Cu deposit is located in the North section of the Dahutang ore field, northern Jiangxi Province, South China. Vein- and breccia-style tungsten-copper mineralization is genetically associated with Mesozoic S-type granitic rocks. Infrared and conventional microthermometric studies of both gangue and ore minerals show that the homogenization temperatures for primary fluid inclusions in wolframite ( 340 °C) are similar to those in scheelite ( 330 °C), but about 40 °C higher than those of apatite ( 300 °C) and generally 70 °C higher than those in coexisting quartz ( 270 °C). Laser Raman analysis identifies CH4 and N2 without CO2 in fluid inclusions in scheelite and coexisting quartz, while fluid inclusions in quartz of the sulfide stage have variable CO2 content. The ore-forming fluids overall are characterized by high- to medium-temperature, low-salinity, CH4, N2, and/or CO2-bearing aqueous fluids. Chalcopyrite, muscovite, and sphalerite are the most abundant solids recognized in fluid inclusions from different ores. The H-O-S-Pb isotope compositions favor a dominantly magmatic origin for ores and fluids, while some depleted δ34S values (- 14.4 to - 0.9‰) of sulfides from the sulfide stage are most likely produced by an increase of oxygen fugacity, possibly caused by inflow of oxidized meteoric waters. The microthermometric data also indicate that a simple cooling process formed early scheelite and wolframite. However, increasing involvement of meteoric waters and fluid mixing may trigger a successive deposition of base metal sulfides. Fluid-rock interaction was critical for scheelite mineralization as indicated by in-situ LA-ICP-MS analysis of trace elements in scheelite.

  17. Genesis of the Silsilah tin deposit, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Kamilli, Robert J.; Criss, R.E.

    1996-01-01

    The Silsilah tin deposit (lat 25 degrees 06' N, long 42 degrees 40' E) consists of a group of pervasively greisenized, flat-topped granite cupolas within a 12-km-diam ring complex. The greisens contain varying amounts of disseminated cassiterite and wolframite. Several types of quartz veins are peripheral to the greisens; some of these contain minor wolframite. The deposit is genetically associated with a highly differentiated, peraluminous alkali-feldspar granite (587 + or - 8 Ma) that is part of a mostly peralkaline, igneous ring complex intruded into Late Proterozoic, immature sandstones of the Murdama Group. We recognize four distinct phases of the peraluminous granite. Only the smallest, most highly differentiated cupolas contain significant tin greisen mineralization. Greisens developed beneath aplitic carapaces that overlie the granite and created impermeable barriers to rising volatiles. The geometry of a cupola correlates strongly with the intensity of alteration; cupolas with the smallest cross sectional areas and steepest marginal contacts have the most intensely greisenized apexes. The paragenetic sequence can be divided into five stages: pegmatite formation, locally pervasive albitization, locally pervasive greisenization and deposition of cassiterite, deposition of quartz-wolframite veins, and deposition of quartz veins with minor base metal sulfides. Pressure-corrected fluid inclusion filling temperatures indicate that the hydrothermal system generally cooled as it evolved and that the delta 18O values of the hydrothermal quartz increased from 10.8 to 15.7 per mil. Calculated delta 18O values of the hydrothermal fluid varied concomitantly from the pegmatite stage (delta 18O fluid approximately 8.6ppm; T [asymp] 550 degrees C) to the greisen stage (5.4 and 5.6[ppm; T [asymp] 360 degrees C), the quartz-wolframite vein stage (6.3 and 7.5ppm; T [asymp] 390 degrees C), and the late vein stage (4.0 and 5.1ppm; T [asymp] 270 degrees C). This evolution probably reflects the admixture of generally increasing amounts of meteoric or formation water having a lower delta 18 O value into the cooling magmatic hydrothermal system. In delta 18O-delta 18O plots for mineral separates from fresh to altered samples of the peraluminous granite the values for quartz and feldspar conform to a steep, positive-sloped disequilibrium trend that indicates interaction with high 18O hydrothermal fluid, mirrored by a negative-sloped disequilibrium trend for quartz and mica. These complementary trends suggest strongly that individual granite cupolas were essentially closed systems during alteration. To our knowledge, this is the first oxygen isotope demonstration of a closed-system, hydrothermal metal deposit. The sandstone country rock has whole-rock delta 18O values of 12.4 + or - 2.0 per mil. The highest values (>13ppm) form a approximately 3-km-wide high delta 18O annulus immediately peripheral to the ring complex. The data suggest that the country rocks were pervasively exchanged with an outward-migrating, high delta 18O fluid moving down a temperature gradient. This fluid was probably formation water that flowed radially inward toward the pluton at a deeper level, forming a largely horizontal, unicellular flow system that had fluid-flow lines nearly vertical next to the intrusion, and directed upward and outward at higher levels. Low delta 18O fluids that formed quartz associated with the tin-tungsten mineralization and later veins are inferred to be the result of a subsequent and distinct phase of the hydrothermal system. Almost all the geologic processes necessary for the formation of an economically viable tin deposit occurred at Silsilah, but the lack of a strong localizing mechanism for cassiterite mineralization resulted in an economically marginal deposit. If the greisenized cupolas had been vertically stacked, as are the intrusions and ore zones in Climax-type molybdenum deposits, or if the mineralizing fluids had been channeled into veins, as in the tin deposits in Cornwall, England, a higher grade deposit might have formed. The generally closed-system behavior of the hydrothermal system at Silsilah may have prevented additional scavenging of metals and the formation of a larger, richer deposit.

  18. Photoassisted carbon dioxide reduction and formation of twoand three-carbon compounds. [prebiological photosynthesis

    NASA Technical Reports Server (NTRS)

    Halmann, M.; Aurian-Blajeni, B.; Bloch, S.

    1981-01-01

    The photoassisted reduction of aqueous carbon dioxide in the presence of naturally occurring minerals is investigated as a possible abiotic precursor of photosynthesis. Aqueous carbon dioxide saturated suspensions or surfaces of the minerals nontronite, bentonite, anatase, wolframite, molybdenite, minium, cinnabar and hematite were irradiated with high-pressure mercury lamps or sunlight. Chemical analyses reveal the production of formic acid, formaldehyde, methanol and methane, and the two and three-carbon compounds glyoxal (CHOCHO) and malonaldehyde (CH2(CHO)2). It is suggested that such photosynthetic reactions with visible light in the presence of semiconducting minerals may provide models for prebiological carbon and nitrogen fixation in both oxidized and reduced atmospheres.

  19. Granite-related Yangjiashan tungsten deposit, southern China

    NASA Astrophysics Data System (ADS)

    Xie, Guiqing; Mao, Jingwen; Li, Wei; Fu, Bin; Zhang, Zhiyuan

    2018-04-01

    The Yangjiashan scheelite-bearing deposit (38,663 metric tons of WO3 with an average ore grade of 0.70% WO3) is hosted in quartz veins in a biotite monzogranite intrusion and surrounding slate in the Xiangzhong Metallogenic Province of southern China. The monzogranite has a zircon SHRIMP U-Pb age of 406.6 ± 2.8 Ma (2σ, n = 20, MSWD = 1.4). Cassiterite coexisting with scheelite yields a weighted mean 206Pb/238U age of 409.8 ± 5.9 Ma (2σ, n = 30, MSWD = 0.20), and molybdenite intergrown with scheelite yields a weighted mean Re-Os age of 404.2 ± 3.2 Ma (2σ, n = 3, MSWD = 0.10). These results suggest that the Yangjiashan tungsten deposit is temporally related to the Devonian intrusion. The δD and calculated δ18OH2O values of quartz intergrown with scheelite range from - 87 to - 68‰, and - 1.2 to 3.4‰, respectively. Sulfides have a narrow range of δ34S values of - 2.9 to - 0.7‰ with an average value of - 1.6‰ (n = 16). The integration of geological, stable isotope, and geochronological data, combined with the quartz-muscovite greisen style of ore, supports a magmatic-hydrothermal origin for the tungsten mineralization. Compared to the more common tungsten skarn, quartz-wolframite vein, and porphyry tungsten deposits, as well as orogenic gold deposits worldwide, the Yangjiashan tungsten deposit is an unusual example of a granite-related, gold-poor, scheelite-bearing quartz vein type of deposit. The calcium needed for the formation of scheelite is derived from the sericitization of calcic plagioclase in the monzogranite and Ca-bearing psammitic country rocks, and the relatively high pH, reduced and Ca-rich mineralizing fluid may be the main reasons for the formation of scheelite rather than wolframite at Yangjiashan.

  20. Characterization and timing of the different types of fluids present in the barren and ore-veins of the W-Sn deposit of Panasqueira, Central Portugal

    NASA Astrophysics Data System (ADS)

    Noronha, F.; Doria, A.; Dubessy, J.; Charoy, B.

    1992-01-01

    The Panasqueira W-Sn deposit is the largest quartz-vein type deposit of the Iberian Peninsula and the most important wolframite deposit in Western Europe. The ore-veins are almost exclusively sub-horizontal. Besides ore-bearing sub-horizontal veins, the Panasqueira mine also contains barren quartz veins. There are essentially two generations of barren quartz: quartz, contemporaneous with the earliest regional metamorphism (QI), and recrystallized quartz, contemporaneous with the thermal metamorphism related to the granite intrusion (QII). Fluid inclusion studies (microthermometry and Raman) were undertaken in order to distinguish fluids contemporaneous with the barren quartz from those contemporaneous with the ore-bearing quartz (QIII). Fluid inclusion data indicate that the barren and ore-bearing quartz fluids are dominantly aqueous (93 to 98 mol% H2O), with a nearly constant bulk salinity (8 to 12 wt% eq. NaCl), with the quantity of volatile component (determined by Raman spectrometry) higher in QIII, but never greater than 5 mol%. However, the CO2/CH4 + N2 ratio is different for each type of quartz. Volatiles are dominated by CH4 (10 to 96 mol% ZCH4 and/or N2 (3 to 87 mol% ZN2) in the barren quartz and by CO2 (60 to 73 mol% ZCO2) in ore-bearing quartz. The bulk chemical composition of the fluids in QIII is comparable to that found commonly in hydrothermal fluids associated with wolframite mineralization, where Na>K>Ca and HCO3>Cl>SO4. A dispersion in TH (226 to 350 °C) found in QIII, together with a variation in the degree of filling (0.5 to 0.7) and with the consequent variation of fluid densities (0.70 to 0.79), may result from changes in the fluid pressure regime below lithostatic pressure, suggesting vein filling related to tectonic events.

  1. Dielectric properties and phase transition behaviors in (1-x)PbZrO3-xPb(Mg1/2W1/2)O3 ceramics

    NASA Astrophysics Data System (ADS)

    Vittayakorn, Naratip; Charoonsuk, Piyanut; Kasiansin, Panisara; Wirunchit, Supamas; Boonchom, Banjong

    2009-09-01

    The solid solution of lead zirconate [PbZrO3 (PZ)] and lead magnesium tungstate [Pb(Mg1/2W1/2)O3 (PMW)] has been synthesized by the wolframite precursor method. The crystal structure, phase transformations, dielectric and thermal properties of (1-x)PZ-xPMW, where x =0.00-0.10, were investigated. The crystal structure of sintered ceramics was analyzed by x-ray diffraction. Phase-pure perovskite was obtained for all compositions. Furthermore, a change from orthorhombic to rhombohedral symmetry was observed as the mole fraction of increased PMW. As a result, it was found that PbZrO3-Pb(Mg1/2W1/2)O3 undergoes successive transitions from the antiferroelectric phase to the ferroelectric phase to the paraelectric state. The coexistence of orthorhombic and rhombohedral phases in this binary system is located near the composition x =0.1.

  2. Influences of PZT addition on phase formation and magnetic properties of perovskite Pb(Fe0.5Nb0.5)O3-based ceramics

    NASA Astrophysics Data System (ADS)

    Amonpattaratkit, P.; Jantaratana, P.; Ananta, S.

    2015-09-01

    In this work, the investigation of phase formation, crystal structure, microstructure, microchemical composition and magnetic properties of perovskite (1-x)PFN-xPZT (x=0.1-0.5) multiferroic ceramics derived from a combination of perovskite stabilizer PZT and a wolframite-type FeNbO4 B-site precursor was carried out by using a combination of X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) analyzer and vibrating sample magnetometer (VSM) techniques. The addition of PZT phase and its concentration have been found to have pronounced effects on the perovskite phase formation, densification, grain growth and magnetic properties of the sintered ceramics. XRD spectra from these ceramics reveal transformation of the (pseudo) cubic into the tetragonal perovskite structure. When increasing PZT content, the degree of perovskite phase formation and the tetragonality value of the ceramics increase gradually accompanied with the variation of cell volume, the M-H hysteresis loops, however, become narrower accompanied by the decrease of maximum magnetization (Mmax), remanent polarization (Mr), and coercive field (HC).

  3. Separation of thorium ions from wolframite and scandium concentrates using graphene oxide.

    PubMed

    Jankovský, Ondřej; Sedmidubský, David; Šimek, Petr; Klímová, Kateřina; Bouša, Daniel; Boothroyd, Chris; Macková, Anna; Sofer, Zdeněk

    2015-10-14

    The separation of rare metals from the ores and commercially available compounds is an important issue due to the need of their high purity in advanced materials and devices. Important examples of two highly important elements that co-exist in the ores are scandium and thorium. Scandium containing ores and consequently also commercially available scandium compounds often contain traces of thorium which is very difficult to separate. We used graphene oxide for the selective sorption of thorium ions from scandium and thorium mixtures originating from the mined ores as well as from commercially available scandium salts. Our results showed that graphene oxide has an extreme affinity towards thorium ions. After the sorption process the graphene oxide contained over 20 wt% of thorium while the amount of scandium sorbed on GO was very low. This phenomenon of high sorption selectivity of graphene oxide can be applied in industry for the purification of various chemicals containing scandium and for separation of thorium containing mixtures. Alternatively, this methodology can be used for preconcentration of thorium from low-grade ores and its further use in the new generation of nuclear reactors.

  4. Energy band gap and spectroscopic studies in Mn{sub 1-x}Cu{sub x}WO{sub 4} (0 ≤ x ≤ 0.125)

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Mal, Priyanath; Rambabu, P.; Turpu, G. R.

    2016-05-06

    A study on the effect of nonmagnetic Cu{sup 2+} substitution at Mn{sup 2+} site on the structural and energy band gap of the MnWO{sub 4} is reported. Convenient solid state reaction route has been adopted for the synthesis of Mn{sub 1-x}Cu{sub x}WO{sub 4}. X-ray diffraction (XRD) pattern showed high crystalline quality of the prepared samples. Raman spectroscopic studies were carried out to understand the structural aspects of the doping. 15 Raman active modes were identified out of 18, predicted for wolframite type monoclinic structure of MnWO{sub 4}. UV-visible diffuse reflectance spectra were recorded and analyzed to get energy band gapmore » of the studied system and are found in the range of 2.5 eV to 2.04 eV with a systematic decrease with the increase in Cu{sup 2+} concentration. Energy band gap values are verified by Density Functional Theory calculations based on projector augmented wave (PAW) method. The calculated values are in good agreement with the experimental data.« less

  5. Ba'id al Jimalah tungsten prospect, Najd region, Kingdom of Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Lofts, P. G.

    The Ba'id al Jimalah tungsten prospect is located in the NE of the Arabian Shield, at 25°09'N, 42°41'E. Mineralization is associated with a late-Proterozoic, porphyritic microgranite emplaced in folded, fine-grained clastic rocks of the Murdama group, within an aureole of biotite-rich hornfels. The microgranite forms a 30 m-thick sill and numerous smaller sills and dikes cropping out along two low, sub-parallel ridges and several small hills in an area 700 m square. The form of the intrusion at depth is uncertain. It is slightly to intensely sericitized, in places greisenized, and is enriched in Li, F and Rb. Wolframite occurs with minor cassiterite, scheelite and sulfides in quartz veins cutting both microgranite and hornfelsed wall-rock. The veins have a dominant trend of 110-115°, and are thicker and more numerous in the microgranite. Gangue minerals include plagioclase and potassium feldspar, muscovite, sericite, fluorite and minor siderite. A major Najd fault trending 130-135° probably controlled magma emplacement and subsequent hydrothermal and pneumatolytic activity. A percussion drilling program, restricted to the outcrop of the sill on the north ridge, has outlined 800,000 tonnes grading 0.10% WO 3 and 0.01% Sn.

  6. Fluid inclusion gas studies, carrock fell tungsten deposit, england: implications for regional exploration

    NASA Astrophysics Data System (ADS)

    Shepherd, T. J.; Waters, P.

    1984-10-01

    A fluid inclusion investigation of the Carrock Fell tungsten deposit, Northern England, confirms that the quartz-wolframite-scheelite veins associated with the Caledonian Skiddaw Granite are almost exclusively related to an exocontact hydrothermal system developed at the margin of a local cupola. Fluid circulation, as defined by the spatial variation in temperature and H2O/CO2 ratios for inclusions in vein quartz, reveals a strong structural control. The zone of maximum flow, which extends 0 400 m out from the granite contact, is characterised by high H2O/CO2 ratios and corresponds closely with the known distribution of high-grade oreshoots. Based on the fluid inclusion “gas” signature for the Carrock Fell deposit, a distinction can be made between potentially tungstaniferous quartz veins and those related to Cu-Pb-Zn deposits in the absence of diagnostic ore minerals. Also, a regional survey of quartz veins in the Lake District suggests that at several localities the fluids have a close affinity with those at Carrock Fell. This is interpreted as the high-level, distal expression of tungsten mineralisation at depth. Evidence for similar mineralisation elsewhere in the British Caledonides favours those granites in the paratectonic zones of Ireland and southern Scotland.

  7. The mineral industry of Ethiopia: present conditions and future prospects

    NASA Astrophysics Data System (ADS)

    Assefa, Getaneh

    Despite a record of mineral activity that dates back to Biblical times and the occurrence of a wide variety of minerals, as well as continuing efforts to discover major ore deposits, Ethiopia's mineral resources ahve remained of minor importance in the world economy. Mineral production in the last 20 years, for example, forms less than 1% of the estimated GDP. Well known minerals andmineral products available in the country in commercial quantities are: gold, platinum, manganese ore, natural agas, clays and clay products, feldspars, gypsum and anhydrite, slat, lime, limestone, cement, sand, structural and crushed stones, marble, mineral water and pumice. There are also vast reserves of water and geothermal power. Recently discovered deposits (over the last 20 years), with major reserves that may attain an important role in mineral production in the future, include potash salts, copper ore and diatomites. Minerals which are known to occur in Ethiopia, but of which supplies are deficient, or which have not yet been proved to exist in economic quantities are: nickel, iron, chromium, mineral fuels (oil, coal and uranium), sulphur, asbesttos, mica, talc, barytes, fluorites, borates, soda-ash, phosphates, wolframite, abrasives (garnet), molybdenite and vanadium. Within the last few years there has been an increasing appreciation of the economic significance of a mineral industry and a definite attempt to foster it. Mineral ownership is vested in the state are cotnrolled by the MInistry of Mines, Energy and Water Resources. The law relating to foreign investment in mines is liberal. The plans for the future have to provide for detailed and intensive exploration of the country's mineral resources, manufacture and fabrication.

  8. Strategies for increasing student knowledge and understanding about conflict minerals in a mineralogy class

    NASA Astrophysics Data System (ADS)

    Cook, G. W.

    2014-12-01

    Conflict minerals, including their uses and methods of extraction, are associated with significant societal and environmental issues in today's world. Minerals such as columbite-tantalite (also referred to as COLTAN), wolframite, cassiterite and gold are important in electronics manufacturing and have a wide variety of other usages. Mining practices are frequently unsustainable and have significant impacts on the environment; moreover, in many locations, such as the Democratic Republic of the Congo—the epicenter of the conflict mineral trade—major human rights violations are associated with the extraction and production of these minerals. Because conflict minerals represent a relatively new issue, students in geology classes are frequently unfamiliar with the topic and commonly have little understanding of the concerns. In some cases they are completely unaware of the issues. In an introductory mineralogy class at the University of California, San Diego I have introduced a content module into my otherwise traditional curriculum that introduces students to conflict minerals, explains the issues, and delineates the problems our society will face with the continued uses of these natural resources. Most significantly, an assignment has been created and implemented in class that is paired with the content module and is designed to enhance and reinforce student learning. Its goal is to increase awareness of the societal and environmental issues surrounding conflict minerals. Initial results suggest (based on pre and post-tests) that our students have learned significantly from the combination of content, exercise, and assessment and that they are much better informed on the issues of conflict minerals. This model, including the exercise, can be modified and adapted for other introductory classes and learning settings.

  9. Intensive low-temperature tectono-hydrothermal overprint of peraluminous rare-metal granite: a case study from the Dlhá dolina valley (Gemericum, Slovakia)

    NASA Astrophysics Data System (ADS)

    Breiter, Karel; Broska, Igor; Uher, Pavel

    2015-02-01

    A unique case of low-temperature metamorphic (hydrothermal) overprint of peraluminous, highly evolved rare-metal S-type granite is described. The hidden Dlhá dolina granite pluton of Permian age (Western Carpathians, eastern Slovakia) is composed of barren biotite granite, mineralized Li-mica granite and albitite. Based on whole-rock chemical data and evaluation of compositional variations of rock-forming and accessory minerals (Rb-P-enriched K-feldspar and albite; biotite, zinnwaldite and di-octahedral micas; Hf-(Sc)-rich zircon, fluorapatite, topaz, schorlitic tourmaline), the following evolutionary scenario is proposed: (1) Intrusion of evolved peraluminous melt enriched in Li, B, P, F, Sn, Nb, Ta, and W took place followed by intrusion of a large body of biotite granites into Paleozoic metapelites and metarhyolite tuffs; (2) The highly evolved melt differentiated in situ forming tourmaline-bearing Li-biotite granite at the bottom, topaz-zinnwaldite granite in the middle, and quartz albitite to albitite at the top of the cupola. The main part of the Sn, Nb, and Ta crystallized from the melt as disseminated cassiterite and Nb-Ta oxide minerals within the albitite, while disseminated wolframite appears mainly within the topaz-zinnwaldite granite. The fluid separated from the last portion of crystallized magma caused small scale greisenization of the albitite; (3) Alpine (Cretaceous) thrusting strongly tectonized and mylonitized the upper part of the pluton. Hydrothermal low-temperature fluids enriched in Ca, Mg, and CO2 unfiltered mechanically damaged granite. This fluid-driven overprint caused formation of carbonate veinlets, alteration and release of phosphorus from crystal lattice of feldspars and Li from micas, precipitating secondary Sr-enriched apatite and Mg-rich micas. Consequently, all bulk-rock and mineral markers were reset and now represent the P-T conditions of the Alpine overprint.

  10. Reconnaissance study of the Taylor Mountains pluton, southwestern Alaska

    USGS Publications Warehouse

    Hudson, Travis L.; Miller, Marti L.; Klimasauskas, Edward P.; Layer, Paul W.

    2010-01-01

    The Taylor Mountains pluton is a Late Cretaceous to early Tertiary (median age 65 + or ? 2 Ma) epizonal, composite biotite granite stock located about 235 km (145 mi) northeast of Dillingham in southwestern Alaska. This 30 km2 (12 mi2) pluton has sharp and discordant contacts with hornfels that developed in Upper Cretaceous clastic sedimentary rocks of the Kuskokwim Group. The three intrusive phases in the Taylor Mountains pluton, in order of emplacement, are (1) porphyritic granite containing large K-feldspar phenocrysts in a coarse-grained groundmass, (2) porphyritic granite containing large K-feldspar and smaller, but still coarse, plagioclase, quartz, and biotite phenocrysts in a fine-grained groundmass, and (3) fine-grained, leucocratic, equigranular granite. The porphyritic granites have different emplacement histories, but similar compositions; averages are 69.43 percent SiO2, 1.62 percent CaO, 5.23 percent FeO+MgO, 3.11 percent Na2O, and 4.50 percent K2O. The fine-grained, equigranular granite is distinctly felsic compared to porphyritic granite; it averages 75.3 percent SiO2, 0.49 percent CaO, 1.52 percent FeO+MgO, 3.31 percent Na2O, and 4.87 percent K2O. Many trace elements including Ni, Cr, Sc, V, Ba, Sr, Zr, Y, Nb, La, Ce, Th, and Nd are strongly depleted in fine-grained equigranular granite. Trace elements are not highly enriched in any of the granites. Known hydrothermal alteration is limited to one tourmaline-quartz replacement zone in porphyritic granite. Mineral deposits in the Taylor Mountains area are primarily placer gold (plus wolframite, cassiterite, and cinnabar); sources for these likely include scattered veins in hornfels peripheral to the Taylor Mountain pluton. The granite magmas that formed the Taylor Mountains pluton are thought to represent melted continental crust that possibly formed in response to high heat flow in the waning stage of Late Cretaceous subduction beneath interior Alaska.

  11. Modern Sedimentation along the SE Bangladesh Coast Reveal Surprisingly Low Accumulation Rates

    NASA Astrophysics Data System (ADS)

    McHugh, C.; Mustaque, S.; Mondal, D. R.; Akhter, S. H.; Iqbal, M.

    2016-12-01

    Recent sediments recovered along the SE coast of Bangladesh, from Teknaf to Cox's Bazar and drainage basin analyses reveal sediment sources and very low sedimentation rates of 1mm/year. These low rates are surprisingly low given that this coast is adjacent to the Ganges-Brahmaputra Delta with a yearly discharge of 1GT. The Teknaf anticline (elevation 200 m), part of the western Burma fold-thrust belt dominates the topography extending across and along the Teknaf peninsula. It is thought to have begun evolving since the Miocene (Alam et al. 2003 & Allen et al. 2008). Presently the anticline foothills on the west are flanked by uplifted terraces, the youngest linked to coseismic displacement during the 1762 earthquake (Mondal et al. 2015), and a narrow beach 60-200 m in width. Petrography, semi-quantitative bulk mineralogy and SEM/EDX analyses were conducted on sediments recovered along the west coast from 1-4 m deep trenches and three 4-8 m deep drill holes. GIS mapping of drainage basins and quartz-feldspar-lithic (QFL) ternary plots based on grain counting show mixing of sediments from multiple sources: Himalayan provenance of metamorphic and igneous origin (garnet-mostly almandine, tourmaline, rutile, kyanite, zircon, sillimanite and clinopyroxene) similar to Uddin et al. (2007); Brahmaputra provenance of igneous and metamorphic origin (amphibole, epidote, plagioclase 40% Na and 60% Ca, apatite, ilmenite, magnetite, Cr-spinel and garnet-mostly grossular,) as indicated by Garzanti et al. (2010) & Rahman et al. (2016) and Burmese sources (cassiterite and wolframite) (Zaw 1990 & Searle et al. 2007). Low sedimentation rates are the result of two main factors: 1. Strong longshore currents from the south-east that interact with high tidal ranges as evidenced by the morphology of sand waves and ridge and runnel landforms along the beach. 2. Streams draining the Teknaf anticline are dry during the winter and during summer monsoon rains, the sediments bypass the narrow beach and are washed out offshore. These sedimentation patterns together with the offshore reversing monsoon circulation are shaping the coast by contributing to erosion, mixing of sediments and transporting minerals from the Burma drainage basin in the south.

  12. Genesis of the vein-type tungsten mineralization at Nyakabingo (Rwanda) in the Karagwe-Ankole belt, Central Africa

    NASA Astrophysics Data System (ADS)

    Dewaele, S.; De Clercq, F.; Hulsbosch, N.; Piessens, K.; Boyce, A.; Burgess, R.; Muchez, Ph.

    2016-02-01

    The vein-type tungsten deposit at Nyakabingo in the central Tungsten belt of Rwanda is located in the eastern flank of the complex Bumbogo anticlinal structure. The host rock is composed of alternating sequences of sandstones, quartzites, and black pyritiferous metapelitic rocks. Two types of W-mineralized quartz veins have been observed: bedding-parallel and quartz veins that are at high angle to the bedding, which are termed crosscutting veins. Both vein types have been interpreted to have been formed in a late stage of a compressional deformation event. Both vein types are associated with small alteration zones, comprising silicification, tourmalinization, and muscovitization. Dating of muscovite crystals at the border of the veins resulted in a maximum age of 992.4 ± 1.5 Ma. This age is within error similar to the ages obtained for the specialized G4 granites (i.e., 986 ± 10 Ma). The W-bearing minerals formed during two different phases. The first phase is characterized by scheelite and massive wolframite, while the second phase is formed by ferberite pseudomorphs after scheelite. These minerals occur late in the evolution of the massive quartz veins, sometimes even in fractures that crosscut the veins. The ore minerals precipitated from a H2O-CO2-CH4-N2-NaCl-(KCl) fluid with low to moderate salinity (0.6-13.8 eq. wt% NaCl), and minimal trapping temperatures between 247 and 344 °C. The quartz veins have been crosscut by sulfide-rich veins. Based on the similar setting, mineralogy, stable isotope, and fluid composition, it is considered that both types of W-mineralized quartz veins formed during the same mineralizing event. Given the overlap in age between the G4 granites and the mineralized quartz veins, and the typical association of the W deposits in Rwanda, but also worldwide, with granite intrusions, W originated from the geochemically specialized G4 granites. Intense water-rock interaction and mixing with metamorphic fluids largely overprinted the original magmatic-hydrothermal signature.

  13. Fluid evolution of Au-Cu zones in Um Balad area, North Eastern Desert of Egypt: Implications from mineral chemistry and fluid inclusions

    NASA Astrophysics Data System (ADS)

    Abd El Monsef, Mohamed; Salem, Ibrahim; Slobodník, Marek; Ragab, Ahmed

    2018-07-01

    Scanning electron microscope (SEM), Electron microprobe (EMPA) and fluid inclusion studies of the ore body, as well as geochemical analyses of country rocks were performed to determine the nature and characteristics of the mineralizing fluid responsible for Au-Cu deposits in Um Balad area, Northern Eastern Desert of Egypt. The Um Balad Au-Cu deposits are confined to well developed-quartz veins and veinlets cutting through the hosting country rocks. Petrographic and geochemical investigations of the hosting rocks distinguished between two main rock units; 1) metagabbro-diorite rocks with tholeiitic nature derived in island arc/continental margin tectonic regime, and 2) granodiorite rocks formed from calc-alkaline magma in continental margin regime. Wallrock alterations are represented by propylitic and argillic types. The mineralized quartz veins are striking in NE-SW direction and dipping between (35°-45°) in SE direction, other mineralized mafic dykes enriched with auriferous quartz veinlets are trending NE-SW and dipping 70°/SE. The main ore minerals are represented by gold, chalcopyrite, pyrite, sphalerite, malachite, covellite and goethite. While, geffroyite, cuprite, chrysocolla, pseudomalachite, britholite, wolframite, scheelite, hematite and rutile are detected as minor constituents. Fluid inclusions microthermometry and isochore calculations combined with chlorite geothermometry revealed that the Um Balad deposits were formed at temperature ranging from 305 °C to 325 °C and pressure between (100-500 bar). The mineralization had been developed in the shallow levels, beneath the water table at depth of 350-1760 m, rather than common mesothermal vein-type deposits in Egypt. Magmatic water have been suggested as the main source for the mineralized fluid. The transportation of the gold metal seems to be happen as bisulfide complexes in moderately acidic environment. The deposition was resulted from combination of changes in physico-chemical parameters, temperature and pressure plus the instability of the reduced sulfur complexes. A contamination with metamorphic and/or meteoric water was also proposed that has strong influence during the depositional process.

  14. Geology and mineral deposits of the Jabal ash Shumta quadrangle, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Hummel, C.L.; Ankary, Abdullah O.

    1972-01-01

    Rocks, structures, and mineral deposits which are the result of both the older Halaban petro-tectonic cycle and the younker Najd Wrench Fault deformation are present in the Ash Shumta area. Northward-trending belts of granitic rocks and folded, layered metavolcanic and metasedimentary rocks of the Halaban Formation which they intrude represent the effects of the Halaban cycle. These older rocks are everywhere transected and deformed by northwestward- and northeastward-striking fractures and strike-slip faults and by eastward-striking fractures and fracture-controlled silicic dikes which belong to the Najd Wrench Fault deformation. Several kinds of epigenetic mineral deposits of hydrothermal origin are present throughout the Ash Shumta area. All occur in or ape closely associated with structures of the Najd Wrench Fault deformation. The mineralization which produced the deposits is thought to have taken place during the period of deformation which produced the Najd Wrench Fault structures. The hydrothermal deposits include many metalliferous quartz veins most of which occur in three mineralized areas: two major areas at Jabal Ash Shumta and Jabal El Khom in the northern half of the quadrangle and a minor area along Wadj al Boharah in the southeastern part of the quadrangle. The metalliferous lodes possess the only economic potential in the area of the Jabal Ash Shumta quadrangle. These lodes consist mainly of gold and base metal-bearing quartz veins, some of which were mined for gold in ancient times. The mineralized area at Jabal Ash Shumta has the best of these veins. Higher temperature veins with wolframite as a major constituent and beryl as a minor one occur in a granite cupola in the eastern part of the El Khom area. These veins have altered, gneissen-like wall rocks. Although the grade of the veins is low at the surface, the made could increase at depth. The tungsten-bearing veins and El Khom area possess the greatest economic promise in the Jabal Ash Shumta quadrangle. They deserve detailed surface investigation followed if needed by exploration at depth.

  15. Potential risk assessment in stream sediments, soils and waters after remediation in an abandoned W>Sn mine (NE Portugal).

    PubMed

    Antunes, I M H R; Gomes, M E P; Neiva, A M R; Carvalho, P C S; Santos, A C T

    2016-11-01

    The mining complex of Murçós belongs to the Terras de Cavaleiros Geopark, located in Trás-os-Montes region, northeast Portugal. A stockwork of NW-SE-trending W>Sn quartz veins intruded Silurian metamorphic rocks and a Variscan biotite granite. The mineralized veins contain mainly quartz, cassiterite, wolframite, scheelite, arsenopyrite, pyrite, sphalerite, chalcopyrite, galena, rare pyrrhotite, stannite, native bismuth and also later bismuthinite, matildite, joseite, roosveltite, anglesite, scorodite, zavaritskite and covellite. The exploitation produced 335t of a concentrate with 70% of W and 150t of another concentrate with 70% of Sn between 1948 and 1976. The exploitation took place mainly in four open pit mines as well as underground. Three lakes were left in the area. Remediation processes of confination and control of tailings and rejected materials and phytoremediation with macrophytes from three lakes were carried out between 2005 and 2007. Stream sediments, soils and water samples were collected in 2008 and 2009, after the remediation process. Most stream sediments showed deficiency or minimum enrichment for metals. The sequential enrichment factor in stream sediments W>Bi>As>U>Cd>Sn=Ag>Cu>Sb>Pb>Be>Zn is mainly associated with the W>Sn mineralizations. Stream sediments receiving drainage of a mine dump were found to be significantly to extremely enriched with W, while stream sediments and soils were found to be contaminated with As. Two soil samples collected around mine dumps and an open pit lake were also found to be contaminated with U. The waters from the Murçós W>Sn mine area were acidic to neutral. After the remediation, the surface waters were contaminated with F(-), Al, As, Mn and Ni and must not be used for human consumption, while open pit lake waters must also not be used for agriculture because of contamination with F(-), Al, Mn and Ni. In most waters, the As occurred as As (III), which is toxic and is easily mobilized in the drainage system. The remediation promoted a decrease in metals and As concentrations of soils and waters, however the applied processes were not enough to rehabilitate the area. Copyright © 2016 Elsevier Inc. All rights reserved.

  16. Re-Os, Sm-Nd, U-Pb, and stepwise lead leaching isotope systematics in shear-zone hosted gold mineralization: genetic tracing and age constraints of crustal hydrothermal activity

    NASA Astrophysics Data System (ADS)

    Frei, R.; Nägler, Th. F.; Schönberg, R.; Kramers, J. D.

    1998-06-01

    A combined Re-Os, Sm-Nd, U-Pb, and stepwise Pb leaching (PbSL) isotope study of hydrothermal (Mo-W)-bearing minerals and base metal sulfides from two adjacent shear zone hosted gold deposits (RAN, Kimberley) in the Harare-Shamva greenstone belt (Zimbabwe) constrain the timing of the mineralizing events to two periods. During an initial Late Archean event (2.60 Ga) a first molybdenite-scheelite bearing paragenesis was deposited in both shear zone systems, followed by a local reactivation of the shear systems during an Early Proterozoic (1.96 Ga) tectono-thermal overprint, during which base metal sulfides and most of the gold was (re-)deposited. While PbSL has revealed an open-system behavior of the U-Pb systematics in molybdenite and wolframite from the RAN mine, initial Archean Re-Os ages are still preserved implying that this system in these minerals was more resistant to the overprint. A similar retentivity could be shown for the Sm-Nd system in scheelite and powellite associated with the above ore minerals. Re-Os isotopic data from the Proterozoic mineralization in the Kimberley mine point to a recent gain of Re, most pronouncedly affecting Fe-rich sulfides such as pyrrhotite. A significant Re-loss in powellitic scheelite (an alteration phase of molybdenite-bearing scheelite), coupled with a marked loss of U in W-Mo ore minerals, complements the observation of a major Re uptake in Fe-sulfides during oxidizing conditions in a weathering environment. Pyrrhotite under these conditions behaves as an efficient Re-sink. Lead isotope signatures from PbSL residues of molybdenite, powellite, and quartz indicate a continental crustal source and/or contamination for the mineralizing fluid by interaction of the fluids with older sedimentary material as represented by the direct host country rocks. Our investigation reveals the potential of the Re-Os isotopic system applied to crustal hydrothermal ore minerals for genetic tracing and dating purposes. The simplified chemical separation of Re and Os from geological material used in this study, together with improvements of chemical yields, will enable high precision data to be collected rapidly on crustal material with low Os concentrations in the future.

  17. Textural and structural evidence for a predeformation hydrothermal origin of the Tungsten Queen Deposit, Hamme District, North Carolina

    USGS Publications Warehouse

    Foose, M.P.; Slack, J.F.; Casadevall, T.

    1980-01-01

    The Hamme tungsten district is composed of a series of steeply dipping quartz-wolframite veins in the Piedmont of North Carolina. Veins are concentrated near the border of the lower Paleozoic Vance County pluton, along its western contact with green-schist-facies metapelites and metavolcanic rocks of the Carolina slate belt. One of these quartz veins, the Snead-Walker, hosts the Tungsten Queen deposit. The vein is 0 to 10 m thick and trends N 35 degrees E for approximately 3,500 m through slate belt rocks and the granitic pluton. The deposit has been worked to a depth of nearly 520 m and contains eight en echelon ore lodes that plunge 42 degrees to 65 degrees between S 10 degrees E and S 10 degrees W. Ore lodes commonly are encased in thin lenses of quartz-sericite greisen. The principal ore mineral is huebnerite and is accompanied by scattered occurrences of pyrite, sphalerite, galena, chalcopyrite, and tetrahedrite. The gangue is predominantly quartz with minor amounts of fluorite, sericite, and carbonate.Studies of minor structures and mineral textures indicate that both the wall rock and the ore and gangue minerals within the vein have been deformed by at least two events. The first event produced relatively gentle, open, and shallow-plunging folds; later, an intense episode of right-lateral shearing developed steeply plunging, tight folds and numerous northeast-trending shears. This latter deformation also developed a prominent alignment of ore and gangue minerals oblique to the vein walls and may have formed the en echelon distribution of ore lodes.In relatively undeformed parts of the vein, clusters of euhedral huebnerite crystals are oriented perpendicular to vein layering. Some prismatic crystals have terminations with cappings of sulfides and in polished thin section show concentric growth zones. These features are similar to textures found in unmetamorphosed tungsten-bearing hydrothermal vein deposits such as those at Pasto Bueno, Peru; Carrock Fell, England; and Panasqueria, Portugal. The relationships of mineral textures and minor structures indicate that the Tungsten Queen deposit formed by open-space fillings of linear faults or fractures and was subsequently deformed by at least two episodes of folding and shearing.

  18. Geological setting and timing of the cassiterite vein type mineralization of the Kalima area (Maniema, Democratic Republic of Congo)

    NASA Astrophysics Data System (ADS)

    Dewaele, S.; Muchez, Ph; Burgess, R.; Boyce, A.

    2015-12-01

    The Central African Mesoproterozoic Karagwe-Ankole belt in the Great Lakes area (DRCongo, Rwanda, Burundi, Uganda and Tanzania) forms a metallogenic province that hosts a variety of granite-related mineralization, which contains cassiterite, columbite-tantalite, wolframite/ferberite, spodumene and beryl. The Kalima area in the Maniema province of the DRCongo forms one of the most important areas for cassiterite mineralization in the eastern part of the DRCongo, even after many decades of exploitation. The mineralization dominantly consists of quartz veins that are hosted in Mesoproterozoic metasediments at the contact with granitic rocks of the Kalima granite (Avuanga and Yubuli) or directly crosscutting these granitic rocks (Atondo). Only limited - and mainly unmineralized pegmatites - have been described in the Lutshurukuru area. Mineralized quartz veins - and some granite bodies - intruded following the regional tectonic foliation or existing fracture zones, confirming the late-to post-tectonic origin of the fertile granite system. The emplacement of the quartz veins resulted in an alteration of the metasedimentary and granitic host-rocks, mainly resulting in muscovitization, tourmalinization and silicification. Cassiterite itself formed relatively late during vein formation and is associated with muscovite in fractures in or along the margins of the quartz veins. 40Ar-39Ar age dating of muscovite of an unmineralized pegmatite from the Lutshurukuru area gave an excellent plateau age of 1024 ± 5.5 Ma, while the muscovite associated with mineralization gave plateau ages of 986 ± 5.3 Ma for the Atondo deposit and 992.4 ± 5.4 Ma for the Yubuli deposit. The rather large spread in ages between the supposed parental granite/pegmatite and quartz veins is interpreted to reflect different magmatic events in the evolution of a composite granite system, starting at ∼1020 Ma and ending with mineralized quartz vein formation at ∼990 Ma. The latter age corresponds with the U-Pb age reported for columbite-tantalite in the area (993 ± 1 Ma at Kamisuku), which could be interpreted as the primary formation age of a new generation of mineralized pegmatites in the Kalima area, or as the resetting age of the U-Pb system during the ∼990 Ma mineralizing event. Muscovite of a mineralized greisen sample of Avuanga gave a plateau age with relaxed constraints of 1010.3 ± 5.9 Ma, which has been interpreted as a partially resetting of muscovite formed at ∼1020 Ma age, during the ∼990 Ma event.

  19. The age and thermal history of Cerro Rico de Potosi, Bolivia

    USGS Publications Warehouse

    Cunningham, C.G.; Zartman, R.E.; McKee, E.H.; Rye, R.O.; Naeser, C.W.; Sanjines, V.O.; Ericksen, G.E.; Tavera, V.F.

    1996-01-01

    Cerro Rico de Potosi, Bolivia, is the world's largest silver deposit and has been mined since the sixteenth century for silver, and for tin and zinc during the twentieth century, together with by-product copper and lead. The deposit consists primarily of veins that cut an altered igneous body that we interpret to be a dacitic volcanic dome and its underlying tuff ring and explosion breccia. The deposit is compositionally and thermally zoned, having a core of cassiterite, wolframite, bismuthinite, and arsenopyrite surrounded by a peripheral, lower-temperature mineral assemblage consisting principally of sphalerite, galena, lead sulfosalt, and silver minerals. The low-temperature assemblage also was superim-posed on the high-temperature assemblage in response to cooling of the main hydrothermal system. Both the dacite dome and the ore fluids were derived from a larger magmatic hydrothermal source at depth. The dome was repeatedly fractured by recurrent movement on the fault system that guided its initial emplacement. The dome was extruded at 13.8 ?? 0.2 Ma (2??), based on U-Th-Pb dating of zircon. Mineralization and alteration occurred within about 0.3 my of dome emplacement, as indicated by a 40Ar/39Ar date of 13.76 ?? 0.10 Ma (1??) for sericite from the pervasive quartz-sericite-pyrite alteration associated with the main-stage, high-temperature, mineralization. The last thermal event able to reset zircon fission tracks occurred no later than 12.5 ?? 1.1 Ma (1??). as indicated by fission-tract dating. Minor sericite. and magmatic-steam alunite veins, were episodically formed around 11 Ma and between 8.3 and 5.7 Ma; the younger episodes occurring at the time of extensional fracturing at Cerro Rico and widespread volcanism in the adjacent Los Frailes volcanic field. None of these younger events appear to be signific-ant thermal/mineralizing events: the exceptionally flat thermal release pattern of 39Ar from sericite and the results of the fission-tract dating of zircon show that none of the younger events was hot enough, and lasted long enough, to cause significant loss of Ar or annealing of zircon fission tracks. U-Th-Pb dating of zircon cores dicates a Precambrian progenitor for some zircons, and REE analyses of dated samples of hydrothermally altered dacite show the presence of a prominent positive Eu anomaly, which constrains interpretations of the origin and evolution of the magmatic/hydrothermal system.

  20. Zircon U-Pb ages and Sr-Nd-Hf isotopes of the highly fractionated granite with tetrad REE patterns in the Shamai tungsten deposit in eastern Inner Mongolia, China: Implications for the timing of mineralization and ore genesis

    NASA Astrophysics Data System (ADS)

    Jiang, Si-Hong; Bagas, Leon; Hu, Peng; Han, Ning; Chen, Chun-Liang; Liu, Yuan; Kang, Huan

    2016-09-01

    The Shamai tungsten deposit is located in the eastern part of the Central Asian Orogenic Belt (CAOB). Tungsten mineralization is closely related to the emplacement of fine- to medium-grained biotite monzogranite (G1) and porphyritic biotite monzogranite (G2) in the Shamai Granite. NW-trending joints and faults host orebodies in the Shamai Granite and Devonian hornfels. The mineralization is characterized by a basal veinlet zone progressing upwards to a thick vein zone followed by a mixed zone, a veinlet zone, and a thread vein zone at the top. The ore-related alteration typically consists of muscovite, greisen, and hornfels. In order to constrain the timing of the Shamai mineralization and discuss the ore genesis, muscovite Ar-Ar, molybdenite Re-Os, and zircon U-Pb geochronological, geochemical, and Sr-Nd-Hf isotopic studies were completed on the deposit. The U-Pb zircon dating yielded weighted mean ages of 153 ± 1 Ma for G1 and 146 ± 1 Ma for G2. Muscovite from a wolframite-bearing quartz vein yielded an Ar-Ar plateau age of 140 ± 1 Ma, whereas two molybdenite samples yielded identical Re-Os model ages of 137 ± 2 Ma. These two ages are younger than the two monzogranites, suggesting a prolonged magmatic-hydrothermal interaction during tungsten mineralization. Major and trace element geochemistry shows that both G1 and G2 are characterized by high SiO2 and K2O contents, high A/CNK values (1.08-1.40), a spectacular tetrad effect in their REE distribution patterns, and non-CHARAC (charge-and-radius-controlled) trace element behavior. This suggests that both G1 and G2 are highly differentiated peraluminous rocks with strong hydrothermal interaction. The Nd-Hf isotope data for the Shamai Granite (εNd(t) between - 1.9 and + 7.4, ɛHf(t) from 5.2 to 12.8) are largely compatible with the general scenario for much of the Phanerozoic granite emplaced in the CAOB. It is here suggested that the Shamai Granite originated from partial melting of a juvenile lower crust with minor input of upper crustal material caused by the underplating of mafic magma in an extensional setting. It can also be concluded that the prolonged fractional crystallization and magmatic-hydrothermal interactions have contributed to the formation of the Shamai tungsten deposit.

  1. Magmatism and polymetallic mineralization in southwestern Qinzhou-Hangzhou metallogenic belt, South China

    NASA Astrophysics Data System (ADS)

    Huang, Xudong; Lu, Jianjun; Wang, Rucheng; Ma, Dongsheng

    2016-04-01

    As Neoproterozoic suture zone between the Yangtze Block and Cathaysia Block, Qinzhou-Hangzhou metallogenic belt is one of the 21 key metallogenic belts in China. Intensive multiple-aged felsic magmatism and related polymetallic mineralization take place in this belt. Although Neoproterozoic, Paleozoic, Triassic granites and associated deposits have been found in southwestern Qinzhou-Hangzhou metallogenic belt, Middle-Late Jurassic (150-165 Ma) magmatism and related mineralization is of the most importance. Three major kinds of Middle-Late Jurassic granitoids have been distinguished. (Cu)-Pb-Zn-bearing granitoids are slightly differentiated, calc-alkaline and metaluminous dioritic to granodioritic rocks. Sn-(W)-bearing granites contain dark microgranular enclaves and have high contents of REE and HFSE, suggesting affinities of aluminous A-type (A2) granites. W-bearing granites are highly differentiated and peraluminous rocks. (Cu)-Pb-Zn-bearing granitoids have ɛNd(t) values of -11 ˜ -4 and ɛHf(t) values of -12 ˜ -7, corresponding to TDMC(Nd) from 1.4 to 1.8 Ga and TDMC(Hf) from 1.6 to 2.0 Ga, respectively. The ɛNd(t) values of W-bearing granites vary from -11 to -8 with TDMC(Nd) of 1.6 ˜ 1.9 Ga and ɛHf(t) values change from -16 to -7 with TDMC(Hf) of 1.5 ˜ 2.0 Ga. Compared with (Cu)-Pb-Zn-bearing granitoids and W-bearing granites, the Sn-(W)-bearing granites have higher ɛNd(t) (-8 ˜ -2) and ɛHf(t) (-8 ˜ -2) values and younger TDMC(Nd) (1.1 ˜ 1.6 Ga) and TDMC(Hf) (1.2 ˜ 1.8 Ga) values, showing a more juvenile isotopic character. Sn-(W)-bearing granites originate from partial melting of granulitized lower crust involved with some mantle-derived materials. W-bearing granites are derived from partial melting of crust. (Cu)-Pb-Zn-bearing granitoids are also derived from crust but may be influenced by more mantle-derived materials. For (Cu)-Pb-Zn deposits, skarn and carbonate replacement are the most important mineralization types. Cu ore bodies mainly distribute proximally to the plutons and Pb-Zn ore bodies occur as distal parts. Skarn, greisen and quartz vein are the dominant types for Sn-W mineralization. For Sn mineralization, chloritized granite type is also important. Greisen type and chloritized granite type occur in granites, skarn in contact zone between granites and wall rocks and quartz vein in wall rocks. Studies on spatial distribution of ore bodies, metallogenic chronology and as well S-Pb-H-O isotopic characteristics indicate these mineral deposits are genetically related Middle-Late Jurassic magmatic-hydrothermal systems. Mineralogical studies show that apatite can provide useful information for petrogenesis and relationship between various kinds of metal mineralization and specific types of granites. Mineralogical features of magnetite, titanite, biotite and wolframite in granites show that these minerals may be used as indicators discriminating the rare metal mineralization potential of granites.

  2. The solubility of gallium oxide in vapor and two-phase fluid filtration in hydrothermal systems

    NASA Astrophysics Data System (ADS)

    Bychkov, Andrew; Matveeva, Svetlana; Nekrasov, Stanislav

    2010-05-01

    The solubility of gallium and aluminum oxides in gas phase in the system Ga2O3 (Al2O3)-HCl-H2O was studied at 150-350°C and pressure up to saturated vapor. The concentration of gallium increases with the increasing of HCl pressure. The formulae of gallium gaseous specie was determined as GaOHCl2. The constant of gallium oxide solubility reaction was calculated at 150, 200, 250, 300 and 350°C. The concentration of aluminum in gas phase is insignificant in the same conditions. The possibility of gallium transportation in gas phase with small quantity of Al allow to divide this elements in hydrothermal processes with gas phase. The Ga/Al ratio in muscovite can be used as the indicator of gas phase separation and condensation. This indicator was not considered in the geochemical literature earlier. The separation of gas and liquid phases was determined in Akchatau (Kazahstan) and Spokoinoe (Russia) greisen W deposit by carbon isotope fractionation of carbon dioxide in fluid inclusion. The important feature of both ore mains is heterogenization and boiling of ore-forming fluids. Greisen ore bodies are formed as a result of strongly focused solution flow in the T-P gradient fields. It is possible to divide ore bodies of Akchatau in two types: muscovite and quartz. Muscovite type veins are thin and have small metasyntactic zone. Quartz type veins are localized in fault with large vertical extent (500 m) and content the large quantity of wolframite. These veins formed in condition of significant pressure decreasing from 2.5 to 0.5 kbar with fluid boiling. Gas and liquid phase separation specifies the vertical zonality of quartz type veins. The gas phase with the high gallium concentration is separated from a flow of liquid phase. Liquid phase react with the granites forming greisen metasomatites. Condensation of the gas phase in upper parts of massive produces the increasing of Ga/Al ratio in muscovite 3-5 times more, then in granites and bottom part of vein (from 2×10-4 to 8×10-4 mass ratio). The muscovite type veins has no separation between gas and liquid due to there thickness and small pressure gradient. There is no difference in Ga/Al ratio in muscovite from this veins. The Spokoinoe deposit is classified by mineralized dome type. The heterogenization of fluid occurs in H2O-CO2 system for water phase and carbon dioxide with temperature decreasing. Two-phase flow is separated in granite, forming greisen metosomatites. The Ga/Al ratio in rock increase up to 3 times to the upper part of metasomatitic zone. The Ga/Al ratio in muscovite can be applied for other hydrothermal systems for geochemical indicator of gas phase separation and condensation zone determination. This work is supported by RFBR project 10-05-00670 and 10-05-00320.

  3. A new mineral species rossovskyite, (Fe3+,Ta)(Nb,Ti)O4: crystal chemistry and physical properties

    NASA Astrophysics Data System (ADS)

    Konovalenko, Sergey I.; Ananyev, Sergey A.; Chukanov, Nikita V.; Rastsvetaeva, Ramiza K.; Aksenov, Sergey M.; Baeva, Anna A.; Gainov, Ramil R.; Vagizov, Farit G.; Lopatin, Oleg N.; Nebera, Tatiana S.

    2015-11-01

    A new mineral rossovskyite named after L.N. Rossovsky was discovered in granite pegmatites of the Bulgut occurrence, Altai Mts., Western Mongolia. Associated minerals are microcline, muscovite, quartz, albite, garnet of the almandine-spessartine series, beryl, apatite, triplite, zircon, pyrite, yttrobetafite-(Y) and schorl. Rossovskyite forms flattened anhedral grains up to 6 × 6 × 2 cm. The color of the mineral is black, and the streak is black as well. The luster is semi-metallic, dull. Mohs hardness is 6. No cleavage or parting is observed. Rossovskyite is brittle, with uneven fracture. The density measured by the hydrostatic weighing method is 6.06 g/cm2, and the density calculated from the empirical formula is 6.302 g/cm3. Rossovskyite is biaxial, and the color in reflection is gray to dark gray. The IR spectrum contains strong band at 567 cm-1 (with shoulders at 500 and 600 cm-1) corresponding to cation-oxygen stretching vibrations and weak bands at 1093 and 1185 cm-1 assigned as overtones. The reflection spectrum in visible range is obtained. According to the Mössbauer spectrum, the ratio Fe2+:Fe3+ is 35.6:64.4. The chemical composition is as follows (electron microprobe, Fe apportioned between FeO and Fe2O3 based on Mössbauer data, wt%): MnO 1.68, FeO 5.92, Fe2O3 14.66, TiO2 7.69, Nb2O5 26.59, Ta2O5 37.51, WO3 5.61, total 99.66. The empirical formula calculated on four O atoms is: {{Mn}}_{0.06}^{2 + } {{Fe}}_{0.21}^{2 + } {{Fe}}_{0.47}^{3 + } Ti0.25Nb0.51Ta0.43W0.06O4. The crystal structure was determined using single-crystal X-ray diffraction data. The new mineral is monoclinic, space group P2/ c, a = 4.668(1), b = 5.659(1), c = 5.061(1) Å, β = 90.21(1)º; V = 133.70(4) Å3, Z = 2. Topologically, the structure of rossovskyite is analogous to that of wolframite-group minerals. The crystal-chemical formula of rossovskyite is [(Fe3+, Fe2+, Mn)0.57Ta0.32Nb0.11][Nb0.40Ti0.25Fe0.18Ta0.11W0.06]O4. The strongest lines of the powder X-ray diffraction pattern [ d, Å (I, %) ( hkl)] are as follows: 3.604 (49) (110), 2.938 (100) (-1-11), 2.534 (23) (002), 2.476 (29) (021), 2.337 (27) (200), 1.718 (26) (-202), 1.698 (31) (-2-21), 1.440 (21) (-311). The type specimen of rossovskyite is deposited in the Mineralogical Museum of the Tomsk State University, Tomsk, 634050 Russia, with the inventory number 20927.

  4. The late Variscan ferroan granite magmatism of southern Sardinia: inferences from Mo metallogenesis

    NASA Astrophysics Data System (ADS)

    Naitza, Stefano; Conte, Aida Maria; Cuccuru, Stefano; Fadda, Sandro; Fiori, Maddalena; Oggiano, Giacomo; Secchi, Francesco

    2017-04-01

    Metallogeny is a powerful tool to investigate crustal evolution; a good example is offered by the Variscan basement of Sardinia and its Mo deposits. Mo ores are poorly represented in Variscan metallogenic provinces of Europe: however, in Sardinia, numerous small Mo deposits, often associated to Sn, W and F ores, are present, invariably related to an early Permian intrusive peak bracketed at about 290 Ma (Fadda et al., 2015; Naitza et al., 2017). In Sardinia, two main magmatic peaks have been schematized at pre-300 and 290 Ma. In southern Sardinia, the 290 magmatic peak is made up of several intrusive F-bearing rock-suites (Conte et al., 2016), belonging to ilmenite series, showing a slight peraluminous character and mostly classifiable as ferroan granites (sensu Frost and Frost, 2011). Mo-bearing granites form a distinct suite of relatively small plutons, emplaced at very shallow depth (about 1kb) in an exhumed Variscan low-grade basement. Peculiar characters of Mo-bearing granites are the occurrence of greisenized microgranite and granophyre cupolas, with fayalite-bearing pegmatites, and ilmenite, xenotime-(Y), monazite, fluorite, and local topaz as accessory phases. Recently, Conte et al. (2016) interpreted these granites as originated by partial melting of low crustal felsic metaigneous photoliths enriched in granophiles (Mo, Sn, W). Mo ores occur as: a) endo- and exo- quartz-muscovite greisens with molybdenite±Fe-Cu sulphides, and b) quartz-molybdenite±wolframite±Fe-Cu-Zn sulphides±fluorite±topaz hydrothermal veins and stockworks, hosted in granites or in country rocks. Redox state of magmas exerts a strong control on Mo metallogeny, as in Mo districts worldwide ores are usually hosted by high-fO2 magnetite series intrusions (Ishihara, 1981). The close field association of Sardinian Mo mineralization with ferroan, low-fO2 ilmenite-series granites may be explained in terms of Mo-enriched crustal sources of magmas, and very efficient geochemical concentration processes. Mo concentration occurred during latest intrusive phases in granitic cupolas, as local subsolidus reactions. They involve: 1) leaching of Mo5+ and Mo6+ from their primary hosts (e.g., biotites) by Cl- and F-rich fluids under decreasing pH and increasing fH2O and fO2, and 2) transport of Mo cations towards intrusive contacts, where they quickly reacted with Sulphur from country rocks to be reduced as MoS2. Overall, the late Variscan Mo metallogenic peak in Sardinia is a single event located in a short timespan at around 290 Ma. In the early Permian extensional setting of Corsica-Sardinia batholith, a distinct HT/LP event related to melting of mantle lithosphere (Rossi et al., 2015), triggered partial melting of Mo-bearing deep crustal sources, producing the F-bearing ferroan magmas. The singular concentration of Mo-bearing granites could indicate a peculiar compositional character of the Sardinian lower crust. References: Conte A.M. et al. (2016). Proc. 2nd European Mineralogical Conference, Rimini, Italy, 154. Fadda et al. (2015). Proc. 13th Biennial SGA Meeting, Nancy, France, Vol. 2, 721-724. Frost, C. D. and Frost R. B. (2011). J. Petrol. 52, 39-53. Ishihara S. (1981). Econ. Geol., 75th Anniversary Volume, 458-484. Naitza S. et al. (2017). Ore Geol. Rev. 80, 1259-1278. Rossi et al. (2015). Bull. Soc. Géol. France 186, 171-192.

  5. Late-Hercynian intrusion-related gold deposits: An integrated model on the Tighza polymetallic district, central Morocco

    NASA Astrophysics Data System (ADS)

    Éric, Marcoux; Khadija, Nerci; Yannick, Branquet; Claire, Ramboz; Gilles, Ruffet; Jean-Jacques, Peucat; Ross, Stevenson; Michel, Jébrak

    2015-07-01

    Gold have been recently recognized in the Tighza (formerly Jebel Aouam) district, in the Hercynian belt of central Morocco. This district has long been known for its W mineralization, as well as major Pb-Ag-Zn, and minor Sb-Ba deposits, all geographically associated with late-Hercynian calc-alkaline magmatism. Gold mineralization in the district is mainly hosted by thick W-Au quartz veins located around the "Mine granite" small granitic plug. Within the veins, gold grade is highest (up to 70 g/t) close to the granite but rapidly decreases going outward from the granite, defining a perigranitic zoning. Anomalous gold grades have also been measured in hydrothermal skarn layers close to two other granitic plugs (Kaolin granite and Mispickel granite), associated with disseminated As-Fe sulfides. The paragenetic sequence for the W-Au quartz veins shows three stages: (1) an early oxidized stage with wolframite-scheelite associated with early quartz (Q1), (2) an intermediate Bi-As-Te-Mo-Au sulfide stage with loellingite, bismuth minerals and native gold with a later quartz (Q2), restricted to a narrow distance from the granite, and (3) a late lower temperature As-Cu-Zn-(Pb) stage with abundant massive pyrrhotite, arsenopyrite and sphalerite, locally forming independent veins ("pyrrhotite vein"). Both Q1 hyaline and Q2 saccharoidal gold-bearing quartz display aqua-carbonic fluids with minor H2S and Cu and an homogeneous composition (81 mole% H2O, 18 mole% CO2 and about 1 mole% NaCl). The trapping pressure is estimated to 1.5-2 kbar with temperature ranging from 300 to 350 °C. Q1 inclusions have exploded indicating an uplift of the Tighza block, that lead to saccharoidal Q2 quartz deposition with multiphase NaCl-saturated fluid inclusions. 40Ar/39Ar dating demonstrates that the "Mine granite", tungsten skarnoid, scheelite-molybdenite veins, and very likely gold-bearing veins are coeval, emplaced at 286 ± 1 Ma. Multiple and widespread metal sources are indicated by radiogenic isotope studies. Nd and Sr isotope compositions of scheelite and granites suggest the participation of a juvenile component while lead isotopes demonstrate a major participation of the basement. Both gold mineralization and zoning suggest that the system developed at the end of the magmatic activity, accompanying a major transition in magmatic fluid composition. The morphology of the gold-bearing mineralization is dependent of the permeability and the reactivity of host-rocks: focus circulation of fluids through pre-existing tectonic corridors, reactivated by late-Hercynian intrusions favor the formation of large W-type gold veins, while infiltration of fluid within reactive stratigraphic layers gives rise to skarn mineralization. A 40Ar/39Ar date (W1 north vein: 291.8 ± 0.3 Ma) indicates that hydrothermal circulation predates gold and tungsten deposition in open fractures as well as Mine granite emplacement. The W-Au mineralization preceded the onset of a large convective hydrothermal cell around the intrusion that led to the formation of the Pb-Ag-Zn mined veins. The Tighza polymetallic district displays numerous similarities with the R-IRG model that was defined in the American Cordillera, such as thermal and zonation patterns, carbonic hydrothermal fluids and chronology of intrusion and related deposits, but also provides new insight to the R-IRG model such as wide Au-quartz veins instead of sheeted Au-veins, oxidation state of the magma, and Sr-Nd isotopic data. These results establish a major magmatic contribution and discard a direct genetic relationship between gold mineralization and major neighboring Pb-Ag-Zn veins. A large number of classic Pb-Zn district of the Western Hercynides belong to the same clan.

  6. Beryl-bearing pegmatites in the Ruby Mountains and other areas in Nevada and northwestern Arizona

    USGS Publications Warehouse

    Olson, Jerry C.; Hinrichs, E. Neal

    1960-01-01

    Pegmatite occurs widely in Nevada and northwestern Arizona, but little mining has been done for such pegmatite minerals as mica, feldspar, beryl, and lepidolite. Reconnaissance for beryl-bearing pegmatite in Nevada and in part of Mohave County, Ariz., and detailed studies in the Dawley Canyon area, Elko County, Nev., have shown that beryl occurs in at least 11 districts in the region. Muscovite has been prospected or mined in the Ruby and Virgin Mountains, Nev., and in Mohave County, Ariz. Feldspar has been mined in the southern part of the region near Kingman, Ariz., and in Clark County, Nev. The pegmatites in the region range in age from Precambrian to late Mesozoic or Tertiary. Among the pegmatite minerals found or reported in the districts studied are beryl, chrysoberyl, scheelite, wolframite, garnet, tourmaline, fluorite, apatite, sphene, allanite, samarskite, euxenite, gadolinite, monazite, autunite, columbite-tantalite, lepidolite, molybdenite, and pyrite and other sulflde minerals. The principal beryl-bearing pegmatites examined are in the Oreana and Lakeview (Humboldt Canyon) areas, Pershing County; the Dawley Canyon area in the Ruby Mountains, Elko County, Nev.; and on the Hummingbird claims in the Virgin Mountains, Mohave County, Ariz. Beryl has also been reported in the Marietta district, Mineral County; the Sylvania district, Esmeralda County; near Crescent Peak and near Searchlight, Clark County, Nev.; and in the Painted Desert near Hoover Dam, Mohave County, Ariz. Pegmatites are abundant in the Ruby Mountains, chiefly north of the granite stock at Harrison Pass. In the Dawley Canyon area of 2.6 square miles at least 350 pegmatite dikes more than 1 foot thick were mapped, and beryl was found in small quantities in at least 100 of these dikes. Four of these dikes exceed 20 feet in thickness, and 1 is 55 feet thick. A few pegmatites were also examined in the Corral Creek, Gilbert Canyon, and Hankins Canyon areas in the Ruby Mountains.The pegmatite dikes in the Dawley Canyon area intrude granite and metamorphic rocks which consist chiefly of quartzite and schist of probable Early Cambrian age. The granite is of two types: a biotite-muscovite granite that forms the main mass of the stock and albite granite that occurs in the metamorphic rocks near the borders of the stock. The pegmatites were emplaced chiefly along fractures in the granite and along schistosity or bedding planes in the metamorphic rocks.Many of the Dawley Canyon pegmatite dikes are zoned, having several rock units of contrasting mineralogy or grain size formed successively from the walls inward. Aplitic units occur either as zones or in irregular positions in the pegmatite dikes and are a distinctive feature of the Dawley Canyon pegmatites. Some of the aplitic and fine-grained pegmatite units are characterized by thin layers of garnet crystals, forming many parallel bands on outcrop surfaces. The occurrence of aplitic and pegmatitic textures in the same dike presumably indicates abrupt changes in physical-chemical conditions during crystallization, such as changes in viscosity and in content of volatile constituents. Concentrations of 0.1 percent or more beryl, locally more than 1 percent, occur in certain zones in the Dawley Canyon pegmatites. Spectrographic analyses of 23 samples indicate that the BeO content ranges from 0.0017 to 0.003 percent in the albite granite, from ,0.0013 to 0.039 percent in aplitic units in pegmatite, from 0.0005 to 0.10 percent in coarse-grained pegmatite, and from less than 0.0001 to 0.0004 percent in massive quartz veins. The scheelite-beryl deposits at Oreana and in Humboldt Canyon, Pershing County, are rich in beryllium. Twelve samples from the Lakeview (Humboldt Canyon) deposit range from 0.018 to 0.11 percent BeO, but underground crosscuts have failed to intersect similar rock at depth. Beryl locally constitutes as much as 10 percent of the pegmatitic ore at Oreana. The beryl was not recovered during tungsten mining at Oreana and is now in the tailings of the mill at Toulon, Nev. The percentage of beryl is lower than the Oreana ore because of dilution by tailings from other ores milled at Toulon. Beryl has been found in many pegmatite dikes in the Virgin Mountains. Both beryl and chrysoberyl occur in dikes on the Hummingbird claims, north of Virgin Peak, in Mohave County, Ariz. Spectrographic analyses of 5 representative samples of the principal dike on the Hummingbird claims range from 0.055 to 0.11 percent BeO.

  7. Evidence of Nb-Ta mobility in high temperature F-rich fluids evidenced by the La Bosse quartz-Nb-ferberite stockwork (Echassières, French Massif Central).

    NASA Astrophysics Data System (ADS)

    Marignac, C.; Cuney, M.

    2012-04-01

    In the Echassières district (northern French Massif Central), the 310 Ma Beauvoir granite (a P-rich peraluminous RMG) overprints a quartz-ferberite stockwork. The 900 m-deep GPF1 scientific hole shows that the stockwork is split into two parts by the gently dipping Beauvoir intrusion: the upper section (~ 100m thick) occurs in the La Bosse quarry, , and the lower section (≥ 60 m thick) below the granite floor. The root of the stockwork (hypothetic La Bosse granite) has not been reached. The stockwork comprises flat-lying quartz veins (≤ 0.6 m thick) concordant to the regional schistosity of surrounding micaschists, and steep N10-N50°E quartz veins (≤ 0.2 m thick). The two sets result from hydraulic fracturing, and consistently display crack seal features. A family of aplites and aplo-pegmatites dikes follow the same set of fractures, being either later (with partial dissolution of pre-existing quartz veins) or earlier, than the quartz veins. There is no alteration, nor associated mineral other than ferberite, at the La Bosse quarry, whereas micaceous selvages are observed in the lower section. Ferberite display a trend of ferberite enrichment with increasing depth (0.71 to 0.95 Fb mole%). In the La Bosse quarry, three ferberite habitus are present: acicular, lanceolate and prismatic. Acicular crystals are typically nicely zoned, with alternating Nb-rich (4.95±0.94 % Nb2O5) and Nb-poor (1.57±0.38 % Nb2O5) growth bands. Ta (up to 0.30 Ta2O5), Ti and Sn are also enriched in the Nb-rich bands. Nb and Ta incorporation into the ferberite is in the form of columbite, as either true solid solution or nanoinclusions. Lanceolate crystals have a similarly zoned acicular core and a Nb-poor rim (1.08±0.66 % Nb2O5). Prismatic crystals are unzoned and Nb-poor (0.67±0.20 % Nb2O5). In the lower part of the stockwork, the Nb contents are lower (2.17 % Nb2O5 in the Nb-rich bands, 1.36 % in the Nb-poor bands, 0.08 % in the unzoned cortex, 0.15 % in the unzoned prisms). Thus the unusual Nb content of the La Bosse ferberites is correlated to the apparently very distal setting of this quartz system relatively to the parent granite, in contrast with most quartz-W systems in the French Massif Central (Aïssa et al. 1987). When invaded by aplites or aplopegmatites, the ferberite-bearing quartz veins are dissolved, but the ferberites remain apparently unaffected - they are not dissolved by the granite melt. Yet, the acicular and lanceolate crystals have lost their Nb-zoning and display uniform homogenised Nb content. The emplacement of the Beauvoir granite was associated with late magmatic exsolution of an Al- and F-rich, silica undersaturated, hydrothermal fluid that percolated upwards in the surrounding schists (Cuney et al. 1992). When interacting with the quartz veins of the La Bosse stockwork, this fluid precipitated topazites. Again, included ferberites remain apparently unaffected. However, they display microscopic vuggy cavities, successively filled by a Nb-rich ferberite (up to 8.91% Nb2O5) with significant Ta content (up to 0.35 % Ta2O5), a wolframo-ixiolite and a Ta-rich columbite. Later Li-phengite was precipitated from the same magmatic fluid, and was associated with hubnerite enrichment of pre-existing ferberites along Li-phengite-bearing microcracks (down to 0.20 mole % Fb). Ta and Nb are known for their poor solubility in hydrothermal fluids, but the Nb and Ta enrichments observed in the wolframite of La Bosse stockwork show that they can be transported to some extent by F-rich fluids. Aïssa, M., Marignac, C., Weisbrod, A. (1987). Le stockwerk à ferbérite d'Echassières : évolution spatiale et temporelle; cristallochimie des ferbérites. In : Cuney, M., Autran, A. (eds), Echassières : le forage scientifique d'Echassières (Allier). Une clé pour la compréhension des mécanismes magmatiques et hydrothermaux associés aux granites à métaux rares. Mém. GPF, tome 1, 311-334. M Cuney, C Marignac, A Weisbrod (1992). The Beauvoir topaz-lepidolite albitic granite (Massif Central, France). A highly specialized granite with disseminated Sn-Li-Ta-Nb-Be mineralization of magmatic origin. Economic Geology 87, 1776-1794.

  8. Tin

    USGS Publications Warehouse

    Kamilli, Robert J.; Kimball, Bryn E.; Carlin, James F.; Schulz, Klaus J.; DeYoung,, John H.; Seal, Robert R.; Bradley, Dwight C.

    2017-12-19

    Tin (Sn) is one of the first metals to be used by humans. Almost without exception, tin is used as an alloy. Because of its hardening effect on copper, tin was used in bronze implements as early as 3500 B.C. The major uses of tin today are for cans and containers, construction materials, transportation materials, and solder. The predominant ore mineral of tin, by far, is cassiterite (SnO2).In 2015, the world’s total estimated mine production of tin was 289,000 metric tons of contained tin. Total world reserves at the end of 2016 were estimated to be 4,700,000 metric tons. China held about 24 percent of the world’s tin reserves and accounted for 38 percent of the world’s 2015 production of tin.The proportion of scrap used in tin production is between 10 and 25 percent. Unlike many metals, tin recycling is relatively efficient, and the fraction of tin in discarded products that get recycled is greater than 50 percent.Only about 20 percent of the world’s identified tin resources occur as primary hydrothermal hard-rock veins, or lodes. These lodes contain predominantly high-temperature minerals and almost invariably occur in close association with silicic, peraluminous granites. About 80 percent of the world’s identified tin resources occur as unconsolidated secondary or placer deposits in riverbeds and valleys or on the sea floor. The largest concentration of both onshore and offshore placers is in the extensive tin belt of Southeast Asia, which stretches from China in the north, through Thailand, Burma (also referred to as Myanmar), and Malaysia, to the islands of Indonesia in the south. Furthermore, tin placers are almost always found closely allied to the granites from which they originate. Other countries with significant tin resources are Australia, Bolivia, and Brazil.Most hydrothermal tin deposits belong to what can be thought of as a superclass of porphyry-greisen deposits. The hydrothermal tin deposits are all characterized by a close spatial, temporal, and genetic association with highly differentiated, peraluminous porphyritic granite intrusions. The intrusions form pegmatites; disseminated ore; parallel or subparallel, greisen-bordered sheeted veins that either cross-cut the intrusion or are peripheral to it; skarns; and (or) limestone replacements that contain different amounts of cassiterite, molybdenite, and wolframite.The tectonic settings of tin-bearing granites are relatively well understood and of limited variety. Tin and tungsten deposits and their associated igneous rocks are found mainly in continental settings.Historically, prospecting for tin has been carried out by the time-honored methods of panning, drilling, trenching, and assaying. Geophysical and geochemical surveys have been employed to cover large areas more rapidly, isolating areas of possible tin deposits so that drilling can be more effective and less costly. Elemental concentrations and relationships of the lithophile elements, especially barium, lithium, niobium, potassium, rubidium, and zirconium, are the most reliable chemical indicators of ore-forming processes and tin-bearing potential.The average human diet includes an intake of about 10 milligrams per day of tin. Ingestion of tin in significantly greater amounts than 10 milligrams per day may lead to a stomach ache, anemia, and liver and kidney problems. Exposure to some organo-tin compounds can interfere with brain and nervous system function and, in severe cases, can cause death. Extended inhalation of tin oxide—an issue mainly for those people who work in the tin industry—results in a higher potential to develop stannosis, which is a mild disease of the lungs caused by the inhalation of tin-bearing dust. Inorganic tin is poorly absorbed by the body, and no evidence exists for the carcinogenicity of metallic tin and tin compounds in humans.Most placer tin deposits are mined by open pit and (or) dredging methods. Mining of alluvial placers in modern streambeds and riverbeds is likely to increase the amount of sediment delivered downstream. This, combined with potential diversion of rivers and streams, may negatively affect downstream ecosystems. Many of the placer deposits located in Burma, Indonesia, Malaysia, and Thailand are located offshore. Most offshore placer tin deposits are mined by dredging methods, which have the potential to negatively affect benthic, midwater, and pelagic ecosystems.In a congressionally mandated U.S. Department of Defense study of strategic minerals published in 2013, tin has the greatest shortfall amount (insufficient supply to meet demand) at \\$416 million; this amount is more than twice that of antimony ($182 million), which is the strategic mineral with the next largest shortfall amount (U.S. Department of Defense, 2013). The United States imported 75 percent of its tin supply in 2015. During the period 2012–15, these imports were from, in descending order of amount imported, Peru, Indonesia, Malaysia, and Bolivia.A promising advancement concerning research into the origin of tin deposits is the recent development of a reliable method of analyzing tin isotopes in cassiterite. Although the mechanism of transport and deposition of tin is fairly well understood, the means by which tin is incorporated into the parent magma at the points of magma generation and ascent needs further investigation.Tin metallogenic provinces worldwide are well known. Consequently, any undiscovered tin deposits will likely be spatially close to known deposits or extensions of the same.

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