Science.gov

Sample records for al contrib mineral

  1. Lherzolitic versus harzburgitic garnet trends: sampling of extended depth versus extended composition. Reply to the comment by Ivanic et al. 2015

    NASA Astrophysics Data System (ADS)

    Kopylova, M.; Hill, P. J. A.; Russell, J. K.; Cookenboo, H.

    2016-02-01

    Using the Hill et al. (Contrib Mineral Petrol 169:13, 2015. doi: 10.1007/s00410-014-1102-7) modeling technique, we have tested the idea of Ivanic et al. (Contrib Mineral Petrol 164:505-520, 2012) that decompression and metamorphic re-equilibration of garnet with spinel causes garnet zoning perpendicular to the Cr-Ca harzburgitic trend in garnet composition. The modeling confirms that garnet zoning across the harzburgitic trend cannot form without spinel buffering. The harzburgitic trend is very rare because it results from extreme compositional heterogeneity of the mantle at the same depth. In contrast, the common lherzolitic trend requires less diversity in the bulk composition of the mantle, as it can be established with only a few samples of metamorphically re-equilibrated mantle peridotite deriving from a variety of depths.

  2. Thermal magnetic behaviour of Al-substituted haematite mixed with clay minerals and its geological significance

    NASA Astrophysics Data System (ADS)

    Jiang, Zhaoxia; Liu, Qingsong; Zhao, Xiangyu; Jin, Chunsheng; Liu, Caicai; Li, Shihu

    2015-01-01

    Clay minerals and Al-substituted haematite (Al-hm) usually coexist in soils and sediments. However, effects of clay minerals on Al-hm during thermal magnetic measurements in argon environment have not been well studied. In order to quantify such effects, a series of Al-hm samples were synthesized, and were then mixed with clay minerals (illite, chlorite, kaolinite and Ca-montmorillonite). The temperature dependence of magnetic susceptibility curves in an argon environment showed that Al-substituted magnetite was produced during the thermal treatment via the reduction of Al-hm by the clay mineral, which leads to a significant magnetic enhancement of the thermal products. In addition, the reductive capacity varies among different types of clay minerals, that is, illite > chlorite > kaolinite > Ca-montmorillonite. Furthermore, the iron content in the clay minerals and Al content of Al-hm are two predominant factors controlling the reduced haematite content. The iron is released from the clay minerals and provides the reducing agent, while Al decreases the crystallinity of haematite and thus facilitates the chemical reaction. Therefore, the thermal magnetic measurements can be used to quantify the Al content of Al-hm in natural samples. Our study provides significant information for palaeomagnetism and environmental magnetism studies, such as thermal magnetic analysis and palaeomagnetic intensity reconstruction using ancient pottery and kilns.

  3. Cavitation pitting and erosion of Al 6061-T6 in mineral oil and water

    NASA Technical Reports Server (NTRS)

    Rao, B. C. S.; Buckley, D. H.

    1983-01-01

    The authors are currently carrying out a study of the cavitation erosion of different bearing metals and alloys in mineral oils were studied. The variations of weight loss, the pit diameter and depth due to cavitation erosion on Al 6061-T6 in mineral oil and water are presented.

  4. Al-bearing dense hydrous minerals under mantle transition zone and uppermost lower mantle conditions

    NASA Astrophysics Data System (ADS)

    Inoue, T.; Hayashi, K.; Yurimoto, H.

    2013-12-01

    Subducting slabs are supplying water into the deep mantle, and some hydrous minerals may be present in the mantle transition zone and even in the uppermost lower mantle. The water storage capacities of mantle minerals are supposed to be significantly coupled with Al by a substitution with Mg2+, Si4+ or Mg2+ + Si4+, because Al3+ is the trivalent cation, and H+ is the monovalent cation. In this study, we have examined the effect of Al for the water content and the stability of some hydrous phases in the system MgO - Al2O3 - SiO2 - H2O in the mantle transition zone and the uppermost lower mantle condition. The experiments were conducted at 20 - 25 GPa and 1873 - 2273K by MA8-type (KAWAI-type) high pressure apparatus. The samples were sealed by AuPd capsule to prevent the loss of water, and the temperatures were measured by WRe thermocouple. The charges were heated for 1 hour in the desired P-T conditions, and then quenched at the rate of ~1000K/sec by tuning off the electric power supply. After releasing the press load for several hours, the run products were recovered, and then the recovered samples were polished to measure the chemical composition and the H2O contents.. We succeeded to synthesize the Al-bearing hydrous minerals (Al-bearing phase B, Al-bearing superhydrous phase B, Mg-Si bearing δ-AlOOH), and found that the significant coupling of H and Al were occurred in these minerals. The chemical compositions and the lattice parameters are examined by SEM-EDS and microfocus-XRD, and the H2O contents were measured by SIMS. The present chemical formula and the lattice parameters were compared to discuss about the difference between the pure chemical forms. Still more, the substitution mechanisms were considered basically by the chemical compositions and the information of the crystal structures. Our study suggests that water can be stored in the mantle transition zone and the uppermost lower mantle in the form of Al-bearing hydrous minerals or nominally anhydrous

  5. Minerals

    MedlinePlus

    Minerals are important for your body to stay healthy. Your body uses minerals for many different jobs, including keeping your bones, muscles, heart, and brain working properly. Minerals are also important for making enzymes and hormones. ...

  6. Oxygen isotope heterogeneity of the mantle beneath the Canary Islands: a discussion of the paper of Gurenko et al.

    NASA Astrophysics Data System (ADS)

    Day, James M. D.; Macpherson, Colin G.; Lowry, David; Pearson, D. Graham

    2012-07-01

    Gurenko et al. (Contrib Mineral Petrol 162:349-363, 2011) report laser-assisted fluorination (LF) and secondary ionization mass spectrometry (SIMS) 18O/16O datasets for olivine grains from the Canary Islands of Gran Canaria, Tenerife, La Gomera, La Palma and El Hierro. As with prior studies of oxygen isotopes in Canary Island lavas (e.g. Thirlwall et al. Chem Geol 135:233-262, 1997; Day et al. Geology 37:555-558, 2009, Geochim Cosmochim Acta 74:6565-6589, 2010), these authors find variations in δ18Ool (~4.6-6.0 ‰) beyond that measured for mantle peridotite olivine (Mattey et al. Earth Planet Sci Lett 128:231-241, 1994) and interpret this variation to reflect contributions from pyroxenite-peridotite mantle sources. Furthermore, Gurenko et al. (Contrib Mineral Petrol 162:349-363, 2011) speculate that δ18Ool values for La Palma olivine grains measured by LF (Day et al. Geology 37:555-558, 2009, Geochim Cosmochim Acta 74:6565-6589, 2010) may be biased to low values due to the presence of altered silicate, possibly serpentine. The range in δ18Ool values for Canary Island lavas are of importance for constraining their origin. Gurenko et al. (Contrib Mineral Petrol 162:349-363, 2011) took a subset (39 SIMS analyses from 13 grains from a single El Hierro lava; EH4) of a more extensive dataset (321 SIMS analyses from 110 grains from 16 Canary Island lavas) to suggest that δ18Ool is weakly correlated ( R 2 = 0.291) with the parameter used by Gurenko et al. (Earth Planet Sci Lett 277:514-524, 2009) to describe the estimated weight fraction of pyroxenite-derived melt ( Xpx). With this relationship, end-member δ18O values for HIMU-peridotite (δ18O = 5.3 ± 0.3 ‰) and depleted pyroxenite (δ18O = 5.9 ± 0.3 ‰) were defined. Although the model proposed by Gurenko et al. (Contrib Mineral Petrol 162:349-363, 2011) implicates similar pyroxenite-peridotite mantle sources to those proposed by Day et al. (Geology 37:555-558, 2009, Geochim Cosmochim Acta 74:6565-6589, 2010

  7. Effects of Al on mineralogy and kinetics of precipitation of silica minerals under crustal conditions

    NASA Astrophysics Data System (ADS)

    Saishu, H.; Okamoto, A.; Tsuchiya, N.

    2011-12-01

    Silica is a dominant component in the Earth's crust. Dissolution and precipitation processes of silica minerals play significant roles on the spatial and temporal distributions of fluids and rock strength in the crusts. Quartz veins occur ubiquitously in the vicinity of seismogenic zones. However the rate equation of silica precipitation is important to consider the sealing of fractures by quartz on the earthquake cycle, it has not been determined except for precipitation rates on surface reactions (Rimstidt and Barnes, 1980) because of the following reasons: cristobalite and amorphous silica occur in the geothermal areas (Alekseyev et al., 2009) whereas quartz is stable in the crust, precipitation of silica minerals occurs not only on quartz surfaces but also via nucleation processes in fluids, and trace elements including Al, Na and K in solutions affect on the species and kinetics of silica precipitation (Okamoto et al., 2010). In the crust, feldspars are dominant constituents, thus the effects of these minor components are crucial for considering the silica precipitation. We conducted the hydrothermal flow-through experiments to investigate the overall precipitation rate of silica minerals and the effects of Al in the solutions under crustal conditions (430 °C and 31 MPa). The experimental apparatus is similar to that in Okamoto et al. (2010). A blank vessel without any rock/mineral substrates was used for precipitation of silica minerals. The Si-supersaturated solutions (C/Ceq = 3-3.5) were prepared by dissolution of quartz at 350 °C, and the concentration of Al in the input solution was controlled from 0 to 7 ppm by dissolution of albite with different temperatures. The experiments in pure Si solution revealed that the precipitation via nucleation in fluids was approximated as the third-order reaction whereas the precipitation on the pre-existing quartz surfaces was determined as the first-order reaction in Rimstidt and Barnes (1980). Activation energy of

  8. The mineral resource potential of the Wadi al Jarir and Al Jurdhawiyah quadrangles, sheets 25/42C and 25/42D, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Fenton, Michael D.

    1983-01-01

    Areas with potential for metallic mineral deposits in the Wadi al Jarir and Al Jurdhawiyah quadrangles, northeastern Arabian Shield, have been identified by reconnaissance rock geochemistry, inspection of ancient prospects, and interpretation of previous work. The ancient prospects of Abraq Shawfan, Abraq Shawfan South, Ad Du'ibi, Ad Du'ibi West, and Ad Dirabi are not recommended for further study. The Bald al Jimalah East ancient lead-silver mine should be drilled to investigate its mineral potential at depth and to.determine its apparent relationship to the nearby Baid al Jimalah West tungsten-tin prospect. High precious metal and copper contents confirmed at the Jarrar ancient prospect suggest additional study. Preliminary results of core and percussion drilling at the Bald al Jimalah West tungsten-tin prospect indicate that the mineralized rocks decrease in grade with depth and are not suitable for current economic exploitation. Geochemically anomalous areas in both plutonic and layered volcanic and clastic terrane are possible sites of significant base metal, molybdenum, tin, tungsten, and rare-earth element mineralization.

  9. Metallic-mineral assessment of the Aban Al Ahmar quadrangle, sheet 25F, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Kamilli, Robert J.; Arnold, Mark A.; Cole, James C.; Kleinkopf, M. Dean; Lee, Keenan; Miller, William R.; Raines, Gary L.; ,; ,

    1990-01-01

    Comprehensive detailed interdisciplinary study assesses the metallic-mineral-resource potential in the Aban Al Ahmar Quadrangle of the Kingdom of Saudi Arabia, located in the eastern margin of the northeastern Arabian Shield, utilizing techniques of geophysics, geologic mapping, remote sensing and geochemistry. The landscape of the study area is characterized by isolated mountain groups, inselbergs, and local tracts of dissected hills separated by broad, low-relief peneplain. Topics covered include mining and exploration history; geological setting; interpretation of geophysical anomalies; limonitic hydrothermally altered and mineralized rocks; geochemical interpretation; mineral resource potential; skarn deposiits associated with intermediate igneous rocks; gold deposits; tin/tungsten skarn deposits; etc. 

  10. Modification of Ti6Al4V Substrates with Well-defined Zwitterionic Polysulfobetaine Brushes for Improved Surface Mineralization

    PubMed Central

    2015-01-01

    Osteoconductive mineral coatings are beneficial for improving the osteointegration of metallic orthopedic/dental implants, but achieving adequate structural integration between the surface minerals and underlying metallic substrates has been a significant challenge. Here, we report covalent grafting of zwitterionic poly(sulfobetaine methacrylate) (pSBMA) brushes on the Ti6Al4V substrates to promote the surface-mineralization of hydroxyapatite with enhanced surface mineral coverage and mineral-substrate interfacial adhesion. We first optimized the atom transfer radical polymerization (ATRP) conditions for synthesizing pSBMA polymers in solution. Well-controlled pSBMA polymers (relative molecular weight up to 26kD, PDI = 1.17) with high conversions were obtained when the ATRP was carried out in trifluoroethanol/ionic liquid system at 60 °C. Applying identical polymerization conditions, surface-initiated atom transfer radical polymerization (SI-ATRP) was carried out to graft zwitterionic pSBMA brushes (PDI < 1.20) from the Ti6Al4V substrates, generating a stable superhydrophilic and low-fouling surface coating without compromising the bulk mechanic property of the Ti6Al4V substrates. The zwitterionic pSBMA surface brushes, capable of attracting both cationic and anionic precursor ions during calcium phosphate apatite mineralization, increased the surface mineral coverage from 32% to 71%, and significantly reinforced the attachment of the apatite crystals on the Ti6Al4V substrate. This facile approach to surface modification of metallic substrates can be exploited to generate multifunctional polymer coatings and improve the performance of metallic implants in skeletal tissue engineering and orthopedic and dental care. PMID:24828749

  11. Mineral replacement reactions and element mobilization

    NASA Astrophysics Data System (ADS)

    Putnis, Christine V.; Ruiz-Agudo, Encarnacion; King, Helen E.; Hövelmann, Jörn; Renard, François

    2016-04-01

    When a mineral is out of equilibrium with an aqueous fluid, reactions will take place in an attempt to reach a new equilibrium. Commonly in the Earth dissolution at a mineral-fluid interface initiates a coupled reaction involving dissolution and precipitation (Ruiz-Agudo et al., 2014). This is a ubiquitous reaction during such processes as metamorphism, metasomatism and weathering. When rock-forming minerals such as feldspars, olivine, pyroxenes are in contact with aqueous fluids (typically NaCl-rich) resultant new phases are formed and elements present in the parent mineral are released to the fluid and therefore mobilized for transport elsewhere. This has been shown in a number of systems such as the albitisation of feldspars (Hövelmann et al., 2010) when a Ca-bearing plagioclase is replaced by albite (NaAlSi3O8). However during this reaction not only is Ca released to the fluid but most other minor elements, such as Mg, Pb, rare earth elements amongst others, are almost totally mobilized and removed in solution. This interface-coupled dissolution-precipitation reaction has many implications for the redistributon of elements in the crust of the Earth. It is also of note that albitisation occurs often in areas of high mineralization, such as in the Curnamona Province in S. Australia (Au-Cu and Ag-Pb-Zn deposits) and the Bamble District of S. Norway. Secondly atomic force microscopy (AFM) has been used to image these reactions at a nanoscale, especially at the calcite-fluid interface, such as the formation of apatite from phosphate-bearing solutions, and the sequestration of toxic elements, eg., Se and As. References Ruiz-Agudo E., Putnis C.V., Putnis A. (2014) Coupled dissolution and precipitation at mineral-fluid interfaces. Chemical Geology, 383, 132-146. Putnis C.V. and Ruiz-Agudo E. (2013) The mineral-water interface: where minerals react with the environment. Elements, 9, 177-182. Hövelmann J., Putnis A., Geisler T., Schmidt B.C., Golla-Schindler U. (2009

  12. Mineral resource assessment of selected areas in Clark and Nye Counties, Nevada [Chapters A-L

    USGS Publications Warehouse

    Ludington, Steve

    2006-01-01

    During 2004-2006, the U.S. Geological Survey conducted a mineral resource assessment of selected areas administered by the Bureau of Land Management in Clark and Nye Counties, Nevada. The purpose of this study is to provide the BLM with information for land planning and management and, specifically, to determine mineral resource potential in accordance with regulations in 43 CFR 2310, which governs the withdrawal of public lands. The Clark County Conservation of Public Land and Natural Resources Act of 2002 (Public Law 107-282) temporarily withdraws a group of areas designated as Areas of Critical Environmental Concern (ACECs) from mineral entry, pending final approval of an application for permanent withdrawal by the BLM. This study provides information about mineral resource potential of the ACECs. Existing information was compiled about the ACECs, including geology, geophysics, geochemistry, and mineral-deposit information. Field examinations of selected areas and mineral occurrences were conducted to determine their geologic setting and mineral potential.

  13. Distribution of Water in Nominally Anhydrous Minerals during Metamorphic Reactions

    NASA Astrophysics Data System (ADS)

    Van Lankvelt, A.; Seaman, S. J.; Williams, M. L.

    2014-12-01

    Nominally anhydrous minerals are a reservoir for water in otherwise dry rocks. This water may play a role in facilitating metamorphic reactions and enhancing deformation. In this study, we examined orthopyroxene-bearing granites from the Athabasca Granulite terrane in northern Saskatchewan. These rocks intruded the lower crust (pressures of 1 GPa) at circa 2.6 Ga at temperatures of > 900 ºC and were subsequently metamorphosed at granulite facies conditions (700 ºC and 1 GPa) in the Paleoproterozoic (Williams et al., 2000). One of the primary reactions recorded by these rocks is locally known as the "Mary" reaction and involves the anhydrous reaction: orthopyroxene + Ca-plagioclase = clinopyroxene + garnet + Na-plagioclase. Measurements of water concentrations in both product and reactant assemblages were performed using a Bruker Vertex 70 Fourier transform infrared spectrometer and revealed that there is a slight excess of water in product minerals over reactant minerals. There are two possible explanations for this. The first is that water was derived from an external source, possibly hydrous, likely contemporaneous, mafic dikes. This interpretation is supported by higher concentrations of K, which is essentially absent from the reactant minerals, in the Na-rich rims of plagioclase. However, only modest amounts of external fluids could have been introduced, or amphiboles would have been stabilized at the expense of clinopyroxene (Moore & Carmichael, 1998). An alternative interpretation is that slightly more water-rich minerals reacted more readily, releasing water that was then incorporated into their products, whereas the water-poorer minerals failed to react. Support for this interpretation comes from very low water concentrations in orthopyroxene and plagioclase from an unreacted and undeformed sample. This interpretation suggests that water in anhydrous minerals may catalyze metamorphic reactions, and a lack of water may be critical for preserving metastable

  14. Low keV electron probe analysis of silicate minerals for Mg, Al, and Si using pure-element standards

    NASA Technical Reports Server (NTRS)

    Cunningham, G. G.

    1972-01-01

    Accurate electron probe values for Mg, Al, and Si in silicate minerals may be obtained with pure-element standards. Analysis must be done at low (6 kV) accelerating potential and for best results, the average atomic number of the sample should be within about plus or minus 1 of the atomic number of the pure-element standard. This last requirement is automatically fulfilled for most common silicate minerals, as their average atomic numbers usually fall within the 11 to 15 range. Examples studied include a wet-chemically analyzed cordierite containing 17.71 weight percent Al, for which a value of 17.6 plus or minus 0.3 percent was obtained with the electron probe, and a hornblende containing 19.15 percent Si, which gave 19.0 plus or minus 0.3 percent using the probe method.

  15. Improved source assessment of Si, Al and related mineral components to PM10 based on a daily sampling procedure.

    PubMed

    Peng, Ge; Puxbaum, Hans; Bauer, Heidi; Jankowski, Nicole; Shi, Yao

    2010-01-01

    Samples obtained from an industrialized valley in the East Alpine region were collected daily for a half year and analyzed using X-ray fluorescence to examine the elements Si, Al, Fe, Ca, Mg, Na, K, Zn, P, S and Cl. Some factors affecting the changes of these elements were considered, including time, elemental correlations, weekday, weekend and seasonal changes. Diagnostic analysis provided an insight into a decoupling behavior that occursin siliceous and carbonates minerals. A decrease in Si and Al and an increase in carbonates, Na, K, Zn and P were observed during the cold season. However, a consistently high correlation of Si and Al was observed in all seasons. It was established that such high levels originated from street surface abrasion. The increase in variability and absolute levels of carbonates during the cold season was demonstrated by adding carbonates to the street surface as gritting material to increase the grip on snowy surfaces. A marked increase in Na and Cl was observed in winter which may have been caused by thaw salt that is widely used in winter in Austria. This was associated with a significant increase in K, Zn, and P in the cold season that was the result of domestic space heating with wood. PM10 levels in December were 12 microg/m3 and were higher than levels detected in July. It was established that such high levels originated from mineral oxides, wood smoke, and inorganic ionic material(s).

  16. The relationship between water content and Al-content in the MTZ and the lower mantle minerals

    NASA Astrophysics Data System (ADS)

    Inoue, T.; Yabuki, T.; Yurimoto, H.

    2011-12-01

    Water is an important volatile component in the Earth mantle, and many high pressure experiments have been conducted so far to determine the stability region of both dense hydrous magnesium silicate (DHMS) and nominally anhydrous minerals with some water. Al3+ is supposed to be coupled with H+ by a substitution with Mg2+, Si4+ or Mg2+ + Si4+. To clarify the degree of the substitution, the water contents and the chemical compositions of Al-bearing minerals in the mantle transition zone and the lower mantle were determined in the systems pyrope - enstatite with H2O of 11.3 wt% and 18.7 wt% at pressures of 20-26 GPa and temperatures of 1473-1873 K, corresponding to the mantle transition zone (MTZ) and the lower mantle. High pressure experiments were conducted by Kawai-type high pressure apparatuses at Ehime University. Starting materials were the mixtures of MgO and SiO2 oxides, and Mg(OH)2 and Al(OH)3 hydroxides with appropriate proportions. We selected the molar ratios of Mg:Si:Al:H = 3:3:1:9 and 3:3:1:5, which H2O contents were 18.7 and 11.3 wt%, respectively, as the starting compositions. The sample was sealed by an AuPd capsule. The recovered charges were polished, and identified by micro-RAMAN spectroscopy, and the chemical compositions for Mg, Si and Al were measured by SEM-EDS at Ehime University. The water contents were measured by secondary ion mass spectrometry (SIMS) at Hokkaido University. In all experimental conditions, hydrous liquid was observed. At 20 GPa, garnet and stishovite was observed, but above 22.5 GPa, phase D was observed instead of garnet in the wide range of the present experimental conditions. At 26 GPa and 1873 K, perovskite was observed. The present phase D included a large amount of Al2O3 (~12-21 wt%), and the Mg/Si molar ratios were ~0.7-0.8. The Al content increased and the Mg/Si ratio decreased, with increasing temperature. Frost and Fei (1998) first reported phase D in the MgO-SiO2-H2O system. Our Mg/Si ratio is ~0.1 larger than

  17. Electron probe microanalysis for high pressure minerals investigation

    NASA Astrophysics Data System (ADS)

    Lavrentiev, Y. G.; Sobolev, N. V.; Korolyuk, V. N.; Usova, L. V.

    2007-12-01

    In the early 1968 in Siberian Branch of the Academy of Sciences of USSR, Novosibirsk, electron probe microanalyzer MS-46 was installed and started to operate for high pressure minerals EPMA investigation. In collaboration with Geophysical Laboratory of Carnegie Institution (Drs. F.R. Boyd, F. Schairer) a set of standards for silicates analysis was developed. Technique for quantitative analysis was developed (Lavrentiev et al., 1974, Zavodsk. Lab., v. 40, p. 657-661) and applied for the first in the USSR analyses of pyropes, associated with Siberian diamonds both as inclusions and xenoliths of diamondiferous peridotites (Sobolev et al., 1969, Dokl. Akad. Nauk SSSR, v. 188, p. 1141-1143; v. 189, p. 162-165). As a result of that research, unique Cr-rich subcalcic pyropes with high knorringite content were found in diamond-bearing kimberlites only and new mineralogical criteria for diamond exploration were developed (Sobolev 1971, Geol. Geofiz., v. 12, p. 70-80) which are still in use worldwide. Further development of electron probe instruments (JXA-5A, Camebax Micro, JXA-8100) and computers, as well as development of analysis technique led to creation of large analytical database. In another field of EPMA - determination of small concentrations of elements - for the first time importance of 0.01-0.3% Na2O admixtures in garnets (Sobolev, Lavrentiev, 1971, Contrib. Min. Petr., v. 31, p. 1-12) and K2O in clinopyroxenes (Sobolev et al., 1970, Dokl. Akad. Nauk SSSR, v. 192, p. 1349-1352) were demonstrated. Since then, determination of sodium content in EPMA of garnets and potassium in pyroxenes became a routine technique. Last generation analyzer (JXA-8100) provided record results down to 6 ppm in detection limit of Ni in pyropes (Lavrentiev et al., Rus. Geol. Geophys., 2006, v. 47, p. 1090-1093). As a result, application of EPMA for single mineral geothermometry (currently based mainly on PIXE method) becomes possible.

  18. Elasticity of Hydrous Aluminosilicate Mineral, Topaz-OH (Al2SiO4(OH)2) at High Pressures

    NASA Astrophysics Data System (ADS)

    Hariharan, A.; Mookherjee, M.; Tsuchiya, J.

    2015-12-01

    We examined the equation of state and high-pressure elasticity of the hydrous aluminosilicate mineral topaz-OH (Al2SiO4(OH)2) using first principles simulation. Topaz-OH is a hydrous phase in the Al2O3-SiO2-H2O (ASH) ternary system, which is relevant for the mineral phase relations in the hydrated sedimentary layer of subducting slabs. Based on recent experiments, it is known that the protons in the topaz-OH exhibit positional disorder with half occupancy over two distinct crystallographic sites. In order to adequately depict the proton environment in the topaz-OH, we examined five crystal structure models with distinct configuration for the protons. Upon full geometry optimization, we find that there are two distinct crystal structures for the topaz-OH. The first crystal structure has an orthorhombic Pbnm space group symmetry, and the second crystal structure has a monoclinic P21/c space group symmetry. At static conditions, the monoclinic (P21/c) topaz-OH has lower energy compared to the orthorhombic (Pbnm) topaz-OH. The energy of the monoclinic (P21/c) topaz-OH remains stable at least up to 40 GPa, i.e., pressures beyond the thermodynamic stability of the topaz-OH. Based on the results from first principles simulation, the equation of state for the monoclinic topaz-OH is well represented by a third-order Birch-Murnaghan formulation, with V0 = 348.63 (±0.04) Å3, K0 = 164.7 (±0.04) GPa, and K'0 = 4.24 (±0.05). The equation of state for the orthorhombic topaz-OH is well represented by a third-order Birch-Murnaghan formulation, with V0 = 352.47 (±0.04) Å3, K0 = 166.4 (±0.06) GPa, and K'0 = 4.03 (±0.04). While the bulk modulus is very similar for both the monoclinic and orthorhombic topaz-OH, the shear elastic moduli are very sensitive to the position of the proton and the orientation of the hydroxyl (O-H) groups. In the hydrated sedimentary layer of a subducting slab, transformation of a mineral assemblage consisting of coesite (SiO2) and diaspore (AlOOH) to

  19. Pseudosinhalite: discovery of the hydrous MgAl-borate as a new mineral in the Tayozhnoye, Siberia, skarn deposit

    NASA Astrophysics Data System (ADS)

    Schreyer, W.; Pertsev, N. N.; Medenbach, O.; Burchard, M.; Dettmar, D.

    After its initial synthesis as the new compound Mg2Al3B2O9(OH) (Daniels et al. 1997) pseudosinhalite has now been discovered as a new mineral. It occurs, together with hydrotalcite, as a replacement product of sinhalite, MgAlBO4, in an impure marble of the contact metasomatic iron boron deposit of Tayozhnoye in the Aldan Shield of Siberia. Its chemical composition determined by electron microprobe is (wt%): Al2O3 46.88; MgO 25.12; FeO 1.99; B2O3 (calculated) 21.75; H2O (calculated) 2.81 giving a total of 98.55 and leading to the empirical formula (Mg2.00 Fe2+0.09)Σ=2.09 Al2.94 B2O9(OH). The small deviation from the ideal stoichiometry with (Mg+Fe2+):Al≠2:3 may be caused by either solid solution towards, or submicroscopic interlayering with lamellae of, the structurally similar mineral sinhalite. The underlying substitution involving also B and H would be (Mg+Fe)+B=Al+2H. Pseudosinhalite is monoclinic, space group P21/c, with a=7.49(1), b=4.33(1), c=9.85(2) Å β=110.7(1)° V=299(1) Å3 Z=2. Calculated density is 3.508g/cm3. Pseudosinhalite is colourless with white streak and has a vitreous lustre. It is transparent; no fluorescence was detected. There is no cleavage and parting; fractures are concoidal. Optical constants could not be measured properly due to polysynthetic microtwinning, but α<1.72<γ. For synthetic pseudosinhalite α=1.691(1) β=1.713(1) γ=1.730(1) Δ=0.039 2V=80°. The temperature of pseudosinhalite formation was below about 400°C at low pressures and with a hydrous, CO2-bearing fluid participating in the reaction.

  20. Surface mineralization of Ti6Al4V substrates with calcium apatites for the retention and local delivery of recombinant human bone morphogenetic protein-2.

    PubMed

    Liu, Pingsheng; Smits, Jonathan; Ayers, David C; Song, Jie

    2011-09-01

    Titanium alloys are prevalently used as orthopedic prosthetics. Inadequate bone-implant interactions can lead to premature prosthetic loosening and implant failure. Local delivery of osteogenic therapeutics promoting osteointegration of the implant is an attractive strategy to address this clinical challenge. Given the affinity of calcium apatites for bone matrix proteins we hypothesize that titanium alloys surface mineralized with calcium apatites should be explored for the retention and local delivery of osteogenic recombinant human bone morphogenetic protein-2 (rhBMP-2). Using a heterogeneous surface nucleation and growth process driven by the gradual pH elevation of an acidic solution of hydroxyapatite via thermal decomposition of urea, Ti6Al4V substrates were surface mineralized with calcium apatite domains exhibiting good affinity for the substrate. The microstructures, size and surface coverage of the mineral domains as a function of the in vitro mineralization conditions were examined by light and scanning electron microscopy and the surface calcium ion content quantified. An optimal mineralization condition was identified to rapidly (<10h) achieve surface mineral coverage far superior to those accomplished by week long incubation in simulated body fluids. In vitro retention-release profiles of rhBMP-2 from the mineralized and unmineralized Ti6Al4V, determined by an enzyme-linked immunosorbent assay, supported a higher degree of retention of rhBMP-2 on the mineralized substrate. The rhBMP-2 retained on the mineralized substrate after 24h incubation in phosphate-buffered saline remained bioactive, as indicated by its ability to induce osteogenic transdifferentiation of C2C12 myoblasts attached to the substrate. This mineralization technique could also be applied to the surface mineralization of calcium apatites on dense tantalum and titanium and porous titanium substrates.

  1. Geology and mineralization of the Jabal Umm Al Suqian albitized apogranite, southern Najd region, Kingdom of Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Bokhari, M. Madani; Jackson, Norman J.; Al Oweidi, Khalid

    A porphyritic muscovite—albite—microcline microgranite crops out at Jabal Umm Al Suqian, 80 km NE of Bishah. It intrudes alkali-feldspar granite, quartz diorite and a conglomerate composed of dioritic clasts, and is enveloped by a shell of hydrothermally altered, albitized, greisenized and microclinized country rocks. The principal chemical features of the microgranite are: 5-7% Na 2O, Na 2O/K 2O = 1.7, Rb 978 ppm, Sn 94 ppm, and low Ba, Ce, Sr and Zr. Albitized microgranite is highly enriched in F, Nb and Y, and the greisenized assemblages are enriched in F, Li, Rb, Sn and Zn. Mineralization consists of small veins and lenses of fluorite and disseminated minerals such as ixiolite, monazite, bastnaesite, betafite and fluorite, but is not economically significant. The microgranite is probably an apogranite cupola in the roof of an alkali-feldspar granite. Crystallization at about 1 kb total volatile pressure was controlled by (1) variable (0-3 wt. %) F contents which significantly reduced the freezing temperature of the melt and resulted in an albite-rich residue; and (2) progressive decrease in K, which also produced a sodic residuum. K- and F-rich hydrothermal fluids produced the envelope of phyllic alteration. Repetitive increase and decrease in volatile pressure produced rhythmic banding of quartz and alkali feldspar in the upper part of the cupola.

  2. An SEM, EDS and vibrational spectroscopic study of the silicate mineral meliphanite (Ca,Na)2Be[(Si,Al)2O6(F,OH)

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; López, Andrés; Theiss, Frederick L.; Romano, Antônio Wilson; Scholz, Ricardo

    2015-02-01

    The mineral meliphanite (Ca,Na)2Be[(Si,Al)2O6(F,OH)] is a crystalline sodium calcium beryllium silicate which has the potential to be used as piezoelectric material and for other ferroelectric applications. The mineral has been characterized by a combination of scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS) and vibrational spectroscopy. EDS analysis shows a material with high concentrations of Si and Ca and low amounts of Na, Al and F. Beryllium was not detected. Raman bands at 1016 and 1050 cm-1 are assigned to the SiO and AlOH stretching vibrations of three dimensional siloxane units. The infrared spectrum of meliphanite is very broad in comparison with the Raman spectrum. Raman bands at 472 and 510 cm-1 are assigned to OSiO bending modes. Raman spectroscopy identifies bands in the OH stretching region. Raman spectroscopy with complimentary infrared spectroscopy enables the characterization of the silicate mineral meliphanite.

  3. Simmonsite, Na2LiAlF6, a new mineral from the Zapot amazonite-topazzinnwaldite pegmatite, Hawthorne, Nevada, U.S.A

    USGS Publications Warehouse

    Foord, E.E.; O'Connor, J. T.; Hughes, J.M.; Sutley, S.J.; Falster, A.U.; Soregaroli, A.E.; Lichte, F.E.; Kile, D.E.

    1999-01-01

    Simmonsite, Na2LiAlF6, a new mineral of pegmatitic-hydrothermal origin, occurs in a late-stage breccia pipe structure that cuts the Zapot amazonite-topaz-zinnvvaldite pegmatite located in the Gillis Range, Mineral Co., Nevada, U.S.A. The mineral is intimately intergrown with cryolite, cryolithionite and trace elpasolite. A secondary assemblage of other alumino-fluoride minerals and a second generation of cryolithionite has formed from the primary assemblage. The mineral is monoclinic, P21 or P21/m, a = 7.5006(6) A??, b = 7.474(1) A??, c = 7.503(1) A??, ??= 90.847(9) ??, V=420.6(1) A??3, Z = 4. The four strongest diffraction maxima [d(A??), likl, I/I100] are (4.33, 111 and 111, 100); (1.877, 400 and 004, 90); (2.25, 13T, 113, 131 and 311, 70); and (2.65, 220, 202, 022, 60). Simmonsite is pale buff cream with white streak, somewhat greasy, translucent to transparent, Mohs hardness of 2.5-3, no distinct cleavage, subconchoidal fracture, no parting, not extremely brittle, Dm is 3.05(2) g/cm3, and Dc is 3.06(1) g/cm3. The mineral is biaxial, very nearly Isotropie, N is 1.359(1) for ?? = 589 nm, and birefringence is 0.0009. Electron microprobe analyses gave (wt%) Na = 23.4, Al = 13.9, F = 58.6, Li = 3.56 (calculated), with a total of 99.46. The empirical formula (based on 6 F atoms) is Na1.98Li1.00 ooAl|ooF6. The crystal structure was not solved, presumably because of unit-cell scale twinning, but similarities to the perovskite-type structure exist. The mineral is named for William B. Simmons, Professor of Mineralogy and Petrology, University of New Orleans, New Orleans.

  4. Temperature assisted radiative and non-radiative recombination mechanisms in sillimanite (Al2SiO5) mineral

    NASA Astrophysics Data System (ADS)

    Kalita, J. M.; Wary, G.

    2017-03-01

    Temperature assisted luminescence in sillimanite (Al2SiO5) mineral was studied using thermoluminescence (TL). TL characteristics were studied in un-annealed and different annealed samples. Analysis showed that in the un-annealed sample, there was four electron trapping sites at depths 0.56, 0.87, 1.08, 1.32 eV and a hole trapping site at depth 3.63 eV from the conduction band acting as a recombination center. Further analysis on the annealed samples showed that the 0.56 eV trapping site was a pressure induced surface trap and it disappeared after annealing. However, the other trapping and recombination sites were found to be stable under thermal treatment. Due to this trap distribution, three partially overlapping glow peaks were observed. The glow peaks were found to be affected by thermal quenching. The thermal quenching parameters were evaluated from the composite glow curves by using Computerized Resolved Peak (CRP) technique. The activation energies for thermal quenching (W) estimated from the three peaks were found to be 0.69 ± 0.05, 0.92 ± 0.06 and 1.15 ± 0.03 eV respectively and the pre-exponential factors (C) were 1.12 × 108, 2.65 × 1010 and 9.23 × 1011 respectively. Based on the analysis, a band model was proposed and the whole radiative and non-radiative recombination mechanisms were discussed.

  5. A vibrational spectroscopic study of the silicate mineral analcime - Na2(Al4SiO4O12)·2H2O - A natural zeolite

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; López, Andrés; Theiss, Frederick L.; Romano, Antônio Wilson; Scholz, Ricardo

    2014-12-01

    We have studied the mineral analcime using a combination of scanning electron microscopy with energy dispersive spectroscopy and vibrational spectroscopy. The mineral analcime Na2(Al4SiO4O12)·2H2O is a crystalline sodium silicate. Chemical analysis shows the mineral contains a range of elements including Na, Al, Fe2+ and Si. The mineral is characterized by intense Raman bands observed at 1052, 1096 and 1125 cm-1. The infrared bands are broad; nevertheless bands may be resolved at 1006 and 1119 cm-1. These bands are assigned to SiO stretching vibrational modes. Intense Raman band at 484 cm-1 is attributed to OSiO bending modes. Raman bands observed at 2501, 3542, 3558 and 3600 cm-1 are assigned to the stretching vibrations of water. Low intensity infrared bands are noted at 3373, 3529 and 3608 cm-1. The observation of multiple water bands indicate that water is involved in the structure of analcime with differing hydrogen bond strengths. This concept is supported by the number of bands in the water bending region. Vibrational spectroscopy assists with the characterization of the mineral analcime.

  6. A vibrational spectroscopic study of the silicate mineral analcime - Na2(Al4SiO4O12)·2H2O - a natural zeolite.

    PubMed

    Frost, Ray L; López, Andrés; Theiss, Frederick L; Romano, Antônio Wilson; Scholz, Ricardo

    2014-12-10

    We have studied the mineral analcime using a combination of scanning electron microscopy with energy dispersive spectroscopy and vibrational spectroscopy. The mineral analcime Na2(Al4SiO4O12)·2H2O is a crystalline sodium silicate. Chemical analysis shows the mineral contains a range of elements including Na, Al, Fe(2+) and Si. The mineral is characterized by intense Raman bands observed at 1052, 1096 and 1125cm(-1). The infrared bands are broad; nevertheless bands may be resolved at 1006 and 1119cm(-1). These bands are assigned to SiO stretching vibrational modes. Intense Raman band at 484cm(-1) is attributed to OSiO bending modes. Raman bands observed at 2501, 3542, 3558 and 3600cm(-1) are assigned to the stretching vibrations of water. Low intensity infrared bands are noted at 3373, 3529 and 3608cm(-1). The observation of multiple water bands indicate that water is involved in the structure of analcime with differing hydrogen bond strengths. This concept is supported by the number of bands in the water bending region. Vibrational spectroscopy assists with the characterization of the mineral analcime.

  7. Arangasite, Al2(PO4)(SO4)F · 7.5H2O, a new mineral from the Alyaskitovy deposit, Eastern Yakutia, Russia

    NASA Astrophysics Data System (ADS)

    Gamyanin, G. N.; Zayakina, N. V.; Galenchikova, L. T.

    2014-12-01

    A new hydrous aluminum sulfate-phosphate-fluoride arangasite, Al2(PO4)(SO4)F · 7.5H2O, has been found in cassiterite-silicate-sulfide ore at the Alyaskitovy deposit, Indigirka River basin, eastern Sakha (Yakutia) (64°39' N, 142°70' E). The new mineral was named after its type locality, Arangas Creek. It belongs to the secondary minerals of the oxidation zone and occurs in cavities within quartz-muscovite-tourmaline-sulfide veins and adjacent greisen. Arangasite is associated with other secondary minerals: phosphorscorodite, fluellite, gypsum, colquiriite, strengite, mansfieldite, and sinkankasite. Arangasite forms white compact segregations composed of fine-lamellar aggregates. This paper reports data on its chemical composition, optical, radiographic, thermal, and IR-spectroscopic characteristics.

  8. SEM, EDX and vibrational spectroscopic study of the mineral tunisite NaCa2Al4(CO3)4Cl(OH)8.

    PubMed

    Frost, Ray L; López, Andrés; Scholz, Ricardo; de Oliveira, Fernando A N

    2015-02-05

    The mineral tunisite has been studied by using a combination of scanning electron microscopy with energy dispersive X-ray fluorescence and vibrational spectroscopy. Chemical analysis shows the presence of Na, Ca, Al and Cl. SEM shows a pure single phase. An intense Raman band at 1127 cm(-1) is assigned to the carbonate ν1 symmetric stretching vibration and the Raman band at 1522 cm(-1) is assigned to the ν3 carbonate antisymmetric stretching vibration. Infrared bands are observed in similar positions. Multiple carbonate bending modes are found. Raman bands attributable to AlO stretching and bending vibrations are observed. Two Raman bands at 3419 and 3482 cm(-1) are assigned to the OH stretching vibrations of the OH units. Vibrational spectroscopy enables aspects of the molecular structure of the carbonate mineral tunisite to be assessed.

  9. Raman spectroscopy of the multi-anion mineral schlossmacherite (H 3O,Ca)Al 3(AsO 4,PO 4,SO 4) 2(OH) 6

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; Palmer, Sara J.; Xi, Yunfei

    2012-02-01

    The mineral schlossmacherite (H 3O,Ca)Al 3(AsO 4,PO 4,SO 4) 2(OH) 6, a multi-cation-multi-anion mineral of the beudantite mineral subgroup has been characterised by Raman spectroscopy. The mineral and related minerals functions as a heavy metal collector and is often amorphous or poorly crystalline, such that XRD identification is difficult. The Raman spectra are dominated by an intense band at 864 cm -1, assigned to the symmetric stretching mode of the AsO 43- anion. Raman bands at 809 and 819 cm -1 are assigned to the antisymmetric stretching mode of AsO 43-. The sulphate anion is characterised by bands at 1000 cm -1 ( ν1), and at 1031, 1082 and 1139 cm -1 ( ν3). Two sets of bands in the OH stretching region are observed: firstly between 2800 and 3000 cm -1 with bands observed at 2850, 2868, 2918 cm -1 and secondly between 3300 and 3600 with bands observed at 3363, 3382, 3410, 3449 and 3537 cm -1. These bands enabled the calculation of hydrogen bond distances and show a wide range of H-bond distances.

  10. Lead exchange into zeolite and clay minerals: A [sup 29]Si, [sub 27]Al, [sup 23]Na solid-state NMR study

    SciTech Connect

    Liang, J.J.; Sherriff, B.L. )

    1993-08-01

    Chabazite, vermiculite, montmorillonite, hectorite, and kaolinite were used to remove Pb, through ion exchange, from 0.01 M aqueous Pb(NO[sub 3])[sub 2] solutions. These minerals contained 27 (Na-chabazite), 16, 9, 9, and 0.5 wt % of Pb, respectively, after equilibration with the solutions. Ion exchange reached equilibrium within 24 h for Na-chabazite and vermiculite, but in less than 5 min for montmorillonite and hectorite. Na-chabazite took up more Pb than natural (Ca, Na)-chabazite (7 wt % Pb), whereas no such difference was observed in different cation forms of the clay minerals. Calcite impurities, associated with the clay minerals, effectively removed Pb from the aqueous solutions by the precipitation of cerussite (PbCO[sub 3]). [sup 29]Si, [sup 27]Al, and [sup 23]Na magic angle spinning (MAS) nuclear magnetic resonance (NMR), [sup 23]Na double rotation (DOR) NMR, and [sup 23]Na variable-temperature MAS NMR were used to study the ion exchange mechanisms. In Na-chabazite, cations in all three possible sites take part in the fast chemical exchange. The chemical exchange passes from the fast exchange regime to the slow regime at [minus]80 to [minus]100[degrees]C. One site contains a relatively low population of exchangeable cations. The other two more shielded sites contain most of the exchangeable cation. The exchangeable cations in chabazite and vermiculite were found to be close to the SiO[sub 4] and AlO[sub 4] tetrahedra, while those in the other clay minerals were more distant. Two sites (or groups of sites) for exchangeable cations were observed in hectorite. Lead tended to occupy the one which corresponds to the [minus]8 ppM peak on the [sup 23]Na MAS NMR spectrum. The behavior of the exchangeable cations in the interlayer sites was similar in all the clay minerals studied. 27 refs., 7 figs., 4 tabs.

  11. Ab initio calculations of Li and B equilibrium isotope fractionation between high -P and -T minerals and aqueous fluids

    NASA Astrophysics Data System (ADS)

    Kowalski, P.; Jahn, S.; Wunder, B.

    2011-12-01

    : staurolite-fluid-mica-spodumene for Li [1] and fluid-tourmaline-B[4] micas for B [2], and reproduce the measured values within accuracy of the measurements and chosen ab initio method. In order to investigate the compression and expansion effects, which influence the fractionation process in high -T and -P materials in the proposed computational approach we treat solids and fluids as continuous media. This allows for modelling the variation of isotope fractionation with the coordination environment of the fractionating element and with pressure and temperature. Our approach is tested by obtaining a good agreement with recent high pressure (P=8GPa) measurements of Li isotopes for spodumene [3] and measurements of B isotopes in differently coordinated states in solids and fluids [2]. [1] Wunder B. et al. (2006) Contrib. Mineral. Petrol. 151, 112-120; Wunder B. et al. (2007) Chem. Geol. 238, 277-290. [2] Meyer et al. (2008) Contrib. Mineral. Petrol. 156, 259-267; Wunder et al. (2005) Lithos 84, 206-216 [3] Wunder, B., Meixner, A., Romer, R. L. and Jahn, S. (2011) Eur. Mineral., in press. DOI: 10.1127/0935-1221/2011/022-2095

  12. Comparison of bio-mineralization behavior of Ti-6Al-4V-1Nb and Zr-1Nb nano-tubes formed by anodization

    NASA Astrophysics Data System (ADS)

    Choi, Yong; Hong, Sun I.

    2014-12-01

    Nano-tubes of titanium and zirconium alloys like Ti-6Al-4V-1Nb and Zr-1Nb were prepared by anodization followed by coating with hydroxylapatite (HA) and their bio-mineralization behaviors were compared to develop a bio-compatible material for implants in orthopedics, dentistry and cardiology. Ti-6Al-4V-1Nb weight gain in a simulated body solution increased gradually. The bigger tube diameter was, the heavier HA was deposited. Surface roughness of both alloys increased highly with the increasing diameter of nano-tube. Their surface roughness decreased by HA deposition due to the removal of the empty space of the nano-tubes. Zr-1Nb alloy had faster growth of nano-tubes layers more than Ti-6Al-4V-1Nb alloy.

  13. A vibrational spectroscopic study of the phosphate mineral vantasselite Al4(PO4)3(OH)3·9H2O

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; Scholz, Ricardo; Belotti, Fernanda Maria; López, Andrés; Theiss, Frederick L.

    2015-08-01

    We have studied the phosphate mineral vantasselite Al4(PO4)3(OH)3·9H2O using a combination of SEM with EDX and Raman and infrared spectroscopy. Qualitative chemical analysis shows Al, Fe and P. Raman bands at 1013 and 1027 cm-1 are assigned to the PO43- ν1 symmetric stretching mode. The observation of two bands suggests the non-equivalence of the phosphate units in the vantasselite structure. Raman bands at 1051, 1076 and 1090 cm-1 are attributed to the PO43- ν3 antisymmetric stretching vibration. A comparison is made with the spectroscopy of wardite. Strong infrared bands at 1044, 1078, 1092, 1112, 1133, 1180 and 1210 cm-1 are attributed to the PO43- ν3 antisymmetric stretching mode. Some of these bands may be due to δAl2OH deformation modes. Vibrational spectroscopy offers a mechanism for the study of the molecular structure of vantasselite.

  14. Using remote sensing techniques and field-based structural analysis to explore new gold and associated mineral sites around Al-Hajar mine, Asir terrane, Arabian Shield

    NASA Astrophysics Data System (ADS)

    Sonbul, Abdullah R.; El-Shafei, Mohamed K.; Bishta, Adel Z.

    2016-05-01

    Modern earth resource satellites provide huge amounts of digital imagery at different resolutions. These satellite imageries are considered one of the most significant sources of data for mineral exploration. Image processing techniques were applied to the exposed rocks around the Al-Aqiq area of the Asir terrane in the southern part of the Arabian Shield. The area under study has two sub-parallel N-S trending metamorphic belts of green-schist facies. The first belt is located southeast of Al-Aqiq, where the Al-Hajar Gold Mine is situated. It is essentially composed of metavolcanics and metasedimentary rocks, and it is intruded by different plutonic rocks of primarily diorite, syenite and porphyritic granite. The second belt is located northwest of Al-Aqiq, and it is composed of metavolcanics and metasedimentary rocks and is intruded by granite bodies. The current study aimed to distinguish the lithological units, detect and map the alteration zones, and extract the major fault lineaments around the Al-Hajar gold prospect. Digital satellite imageries, including Landsat 7 ETM + multispectral and panchromatic and SPOT-5 were used in addition to field verification. Areas with similar spectral signatures to the prospect were identified in the nearby metamorphic belt; it was considered as a target area and was inspected in the field. The relationships between the alteration zones, the mineral deposits and the structural elements were used to locate the ore-bearing zones in the subsurface. The metasedimentary units of the target area showed a dextral-ductile shearing top-to-the-north and the presence of dominant mineralized quartz vein-system. The area to the north of the Al-Hajar prospect showed also sub-parallel shear zones along which different types of alterations were detected. Field-based criteria such as hydrothermal breccia, jasper, iron gossans and porphyritic granite strongly indicate the presence of porphyry-type ore deposits in Al-Hajar metamorphic belt that

  15. Raman spectroscopic study of the mineral qingheiite Na2(Mn2+,Mg,Fe2+)2(Al,Fe3+)(PO4)3, a pegmatite phosphate mineral from Santa Ana pegmatite, Argentina.

    PubMed

    Frost, Ray L; Xi, Yunfei; Scholz, Ricardo; López, Andrés; Moreira, Caio; de Lena, Jorge Carvalho

    2013-10-01

    The pegmatite mineral qingheiite Na2(Mn(2+),Mg,Fe(2+))2(Al,Fe(3+))(PO4)3 has been studied by a combination of SEM and EMP, Raman and infrared spectroscopy. The studied sample was collected from the Santa Ana pegmatite, Argentina. The mineral occurs as a primary mineral in lithium bearing pegmatite, in association with beausite and lithiophilite. The Raman spectrum is characterized by a very sharp intense Raman band at 980 cm(-1) assigned to the PO4(3-) symmetric stretching mode. Multiple Raman bands are observed in the PO4(3-) antisymmetric stretching region, providing evidence for the existence of more than one phosphate unit in the structure of qingheiite and evidence for the reduction in symmetry of the phosphate units. This concept is affirmed by the number of bands in the ν4 and ν2 bending regions. No intensity was observed in the OH stretching region in the Raman spectrum but significant intensity is found in the infrared spectrum. Infrared bands are observed at 2917, 3195, 3414 and 3498 cm(-1) are assigned to water stretching vibrations. It is suggested that some water is coordinating the metal cations in the structure of qingheiite.

  16. Raman spectroscopic study of the mineral qingheiite Na2(Mn2+,Mg,Fe2+)2(Al,Fe3+)(PO4)3, a pegmatite phosphate mineral from Santa Ana pegmatite, Argentina

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; Xi, Yunfei; Scholz, Ricardo; López, Andrés; Moreira, Caio; de Lena, Jorge Carvalho

    2013-10-01

    The pegmatite mineral qingheiite Na2(Mn2+,Mg,Fe2+)2(Al,Fe3+)(PO4)3 has been studied by a combination of SEM and EMP, Raman and infrared spectroscopy. The studied sample was collected from the Santa Ana pegmatite, Argentina. The mineral occurs as a primary mineral in lithium bearing pegmatite, in association with beausite and lithiophilite. The Raman spectrum is characterized by a very sharp intense Raman band at 980 cm-1 assigned to the PO43- symmetric stretching mode. Multiple Raman bands are observed in the PO43- antisymmetric stretching region, providing evidence for the existence of more than one phosphate unit in the structure of qingheiite and evidence for the reduction in symmetry of the phosphate units. This concept is affirmed by the number of bands in the ν4 and ν2 bending regions. No intensity was observed in the OH stretching region in the Raman spectrum but significant intensity is found in the infrared spectrum. Infrared bands are observed at 2917, 3195, 3414 and 3498 cm-1 are assigned to water stretching vibrations. It is suggested that some water is coordinating the metal cations in the structure of qingheiite.

  17. Vibrational spectroscopic characterization of the phosphate mineral kulanite Ba(Fe2+,Mn2+,Mg)2(Al,Fe3+)2(PO4)3(OH)3

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; López, Andrés; Xi, Yunfei; Granja, Amanda; Scholz, Ricardo

    2013-11-01

    The mineral kulanite BaFe2Al2(PO4)3(OH)3, a barium iron aluminum phosphate, has been studied by using a combination of electron microscopy and vibrational spectroscopy. Scanning electron microscopy with EDX shows the mineral is homogenous with no other phases present. The Raman spectrum is dominated by an intense band at 1022 cm-1 assigned to the PO43- ν1 symmetric stretching mode. Low intensity Raman bands at 1076, 1110, 1146, 1182 cm-1 are attributed to the PO43 - ν3 antisymmetric stretching vibrations. The infrared spectrum shows a complex spectral profile with overlapping bands. Multiple phosphate bending vibrations supports the concept of a reduction in symmetry of the phosphate anion. Raman spectrum at 3211, 3513 and 3533 cm-1 are assigned to the stretching vibrations of the OH units. Vibrational spectroscopy enables aspects on the molecular structure of kulanite to be assessed.

  18. The molecular structure of the phosphate mineral senegalite Al2(PO4)(OH)3ṡ3H2O - A vibrational spectroscopic study

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; López, Andrés; Xi, Yunfei; Murta, Natália; Scholz, Ricardo

    2013-09-01

    We have studied the mineral senagalite, a hydrated hydroxy phosphate of aluminium with formula Al2(PO4)(OH)3ṡ3H2O using a combination of electron microscopy and vibrational spectroscopy. Senegalite crystal aggregates shows tabular to prismatic habitus and orthorhombic form. The Raman spectrum is dominated by an intense band at 1029 cm-1 assigned to the PO43- ν1 symmetric stretching mode. Intense Raman bands are found at 1071 and 1154 cm-1 with bands of lesser intensity at 1110, 1179 and 1206 cm-1 and are attributed to the PO43- ν3 antisymmetric stretching vibrations. The infrared spectrum shows complexity with a series overlapping bands. A comparison is made with spectra of other aluminium containing phosphate minerals such as augelite and turquoise. Multiple bands are observed for the phosphate bending modes giving support for the reduction of symmetry of the phosphate anion. Vibrational spectroscopy offers a means for the assessment of the structure of senagalite.

  19. REE Mineralization in Kiruna-type Magnetite-Apatite Ore Deposits: Magmatism and Metasomatism

    NASA Astrophysics Data System (ADS)

    Harlov, D. E.

    2015-12-01

    Magnetite-apatite ore bodies of the Kiruna type occur worldwide and are generally associated with volcanic rocks or volcanism. They also show strong evidence of extensive metasomatism over a wide P-T range. Notable examples include the Kiirunavaara ore body, northern Sweden (Harlov et al., 2002, Chem. Geol., 191, 47-72); the Grängesberg ore body, central Sweden (Jonsson et al., 2010, NGF abstracts, vol 1, 88-89); the Mineville ore body, Adirondacks, New York, USA (McKeown and Klemc, 1956, U.S. Geol Sur Bull (1956), pp. 9-23); the Pea Ridge ore body, SE Missouri, USA (Kerr, 1998, MS Thesis, Univ. Windsor, Windsor, Ontario, Canada 113 pp); the Jurassic Marcona ore body in south-central Peru (Chen et al., 2010, Econ Geol, 105, 1441-1456); and a collection of ore bodies from the Bafq Region, central Iran (Daliran et al., 2010, Geol. Assoc. Canada, Short Course Notes, v. 20, p.147-159). In these ore bodies, low Th and U monazite, xenotime, allanite, REE carbonates, and/or REE fluorides are commonly associated with the apatite as inclusions, rim grains, or as independent grains in the surrounding mineral matrix. High contrast BSE imaging, coupled with EMPA and LA-ICPMS, indicates that the apatite has experienced fluid-induced alteration in the form of (Y+REE) + Na + Si + Cl depletion implying that it served as the source for the (Y+REE) (e.g. Kiirunavaara, northern Sweden; Harlov et al., 2002). Formation of monazite and xenotime associated with fluorapatite, as inclusions or rim grains, has experimentally been demonstrated to originate from the fluorapatite as the result of fluid-aided, coupled dissolution-reprecipitation processes (Harlov et al., 2005, Contrib. Mineral. Petrol. 150, 268-286). This is explains the low Th and U content of the monazite and xenotime. Fluid sources could range from 700-900 °C, residual, acidic (HCl, H2HSO4) grain boundary fluids, remaining after the last stages of ore body crystallization, to later stage, cooler (< 600 °C) (H2O-CO2-(Na

  20. Layered double hydroxide of Cd-Al/C for the Mineralization and De-coloration of Dyes in Solar and Visible Light Exposure

    NASA Astrophysics Data System (ADS)

    Khan, Shahid Ali; Khan, Sher Bahadar; Asiri, Abdullah M.

    2016-11-01

    Cd-Al/C layered double hydroxide (Cd-Al/C-LDH) and Cd-Sb/C nanocatalyst are reported here for the de-coloration and mineralization of organic dyes. These catalysts were largely characterized by FESEM, EDS, XRD, FTIR, XPS, PL and DRS. The diffuse reflectance data showed a band gap at 2.92 and 2.983 eV for Cd-Al/C-LDH and Cd-Sb/C respectively. The band gap suggested that both catalysts work well in visible range. The photoluminescence spectra indicated a peak at 623 nm for both the catalysts which further support the effectiveness of the respective catalyst in visible range. Both catalysts also showed good recyclability and durability till 4th cycle. Five dyes, acridine orange (AO), malachite green (MG), crystal violet (CV), congo red (CR) and methyl orange (MO) were used in this experiment. Various parameters of different light intensity such as visible, ultraviolet, sunlight and dark condition are observed for the de-coloration of these dyes. The de-coloration phenomenon was proceeded through adsorption assisted phot-degradation. The low cost, abundant nature, good recyclability and better dye removal efficiency make these catalysts suitable candidates for the de-coloration and mineralization of organic dyes.

  1. Layered double hydroxide of Cd-Al/C for the Mineralization and De-coloration of Dyes in Solar and Visible Light Exposure

    PubMed Central

    Khan, Shahid Ali; Khan, Sher Bahadar; Asiri, Abdullah M.

    2016-01-01

    Cd-Al/C layered double hydroxide (Cd-Al/C-LDH) and Cd-Sb/C nanocatalyst are reported here for the de-coloration and mineralization of organic dyes. These catalysts were largely characterized by FESEM, EDS, XRD, FTIR, XPS, PL and DRS. The diffuse reflectance data showed a band gap at 2.92 and 2.983 eV for Cd-Al/C-LDH and Cd-Sb/C respectively. The band gap suggested that both catalysts work well in visible range. The photoluminescence spectra indicated a peak at 623 nm for both the catalysts which further support the effectiveness of the respective catalyst in visible range. Both catalysts also showed good recyclability and durability till 4th cycle. Five dyes, acridine orange (AO), malachite green (MG), crystal violet (CV), congo red (CR) and methyl orange (MO) were used in this experiment. Various parameters of different light intensity such as visible, ultraviolet, sunlight and dark condition are observed for the de-coloration of these dyes. The de-coloration phenomenon was proceeded through adsorption assisted phot-degradation. The low cost, abundant nature, good recyclability and better dye removal efficiency make these catalysts suitable candidates for the de-coloration and mineralization of organic dyes. PMID:27841277

  2. Ferroindialite (Fe2+,Mg)2Al4Si5O18, a new beryl-group mineral from the Eifel volcanic region, Germany

    NASA Astrophysics Data System (ADS)

    Chukanov, N. V.; Aksenov, S. M.; Pekov, I. V.; Ternes, B.; Schüller, W.; Belakovskiy, D. I.; Van, K. V.; Blass, G.

    2014-12-01

    A new mineral, ferroindialite, a Fe2+-dominant analog of indialite, has been found in a pyrometamorphosed xenolith of pelitic rock hosted in alkaline basalts. Associated minerals are phlogopite, sanidine, sillimanite, pyroxenes of the enstatite-ferrosilite series, wagnerite, fluorapatite, tridymite, zircon and almandine. Ferroindialite forms brown-purple to gray with a violet-blue tint short prismatic or thick tabular hexagonal crystals up to 1.5 mm in size. The new mineral is brittle, with a Mohs' hardness of 7. Cleavage is not observed. D meas = 2.66(1), D calc = 2.667 g/cm3. IR spectrum shows neither H2O nor OH groups. Ferroindialite is anomalously biaxial (-), α = 1.539(2), β = 1.552(2), γ = 1.554(2), 2 V meas = 30(10)°. The mineral is weakly pleochroic, ranging from colorless on X to pale violet on Z. Dispersion is weak, r < v. The chemical composition (electron microprobe, mean of five point analyses, wt %) is as follows: 0.14 Na2O, 0.46 K2O, 4.95 MgO, 1.13 MnO, 12.66 FeO, 2.64 Fe2O3, 30.45 Al2O3, 47.22 SiO2, total is 99.65. The distribution of total iron content between Fe2+ and Fe3+ was carried out according to structural data. The empirical formula of ferroindialite is: (K0.06Na0.03)(Fe{1.12/2+}Mg0.78Mn0.10)Σ2.00(Al3.79Fe{0.21/3+})Σ4.00Si4.98O18. The simplified formula is: (Fe2+,Mg)2Al4Si5O18. The crystal structure has been refined on a single crystal, R = 0.049. Ferroindialite is hexagonal, space group P6/ mcc; a = 9.8759(3), c = 9.3102(3) Å, V = 786.40(3) Å3, Z = 2. The strongest lines in the X-ray powder diffraction pattern [ d, Å ( I, %) ( hkl)] are: 8.59 (100) (100), 4.094 (27) (102), 3.390 (35) (112), 3.147 (19) (202), 3.055 (31) (211), 2.657 (12) (212), 1.695 (9) (224). The type specimen of ferroindialite is deposited in the Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow, registration number 4400/1.

  3. Vibrational spectroscopic study of the copper silicate mineral ajoite (K,Na)Cu7AlSi9O24(OH)6·3H2O

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; Xi, Yunfei

    2012-06-01

    Ajoite (K,Na)Cu7AlSi9O24(OH)6·3H2O is a mineral named after the Ajo district of Arizona. Raman and infrared spectroscopy were used to characterise the molecular structure of ajoite. The structure of the mineral shows disorder which is reflected in the difficulty of obtaining quality Raman spectra. The Raman spectrum is characterised by a broad spectral profile with a band at 1048 cm-1 assigned to the ν1 (A1g) symmetric stretching vibration. Strong bands at 962, 1015 and 1139 cm-1 are assigned to the ν3 SiO4 antisymmetric stretching vibrations. Multiple ν4 SiO4 vibrational modes indicate strong distortion of the SiO4 tetrahedra. Multiple AlO and CuO stretching bands are observed. Raman spectroscopy and confirmed by infrared spectroscopy clearly shows that hydroxyl units are involved in the ajoite structure. Based upon the infrared spectra, water is involved in the ajoite structure, probably as zeolitic water.

  4. Clay Minerals

    SciTech Connect

    Mueller, Karl T.; Sanders, Rebecca L.; Washton, Nancy M.

    2014-03-14

    Clay minerals are important components of the environment and are involved or implicated in processes such as the uptake of pollutants and the release of nutrients and as potential platforms for a number of chemical reactions. Owing to their small particle sizes (typically, on the order of microns or smaller) and mixing with a variety of other minerals and soil components, advanced characterization methods are needed to study their structures, dynamics, and reactivities. In this article, we describe the use of solid-state NMR methods to characterize the structures and chemistries of clay minerals. Early one-pulse magic-angle spinning (MAS) NMR studies of 27Al and 29Si have now been enhanced and extended with new studies utilizing advanced methodologies (such as Multiple Quantum MAS) as well as studies of less-sensitive nuclei. In additional work, the issue of reactivity of clay minerals has been addressed, including studies of reactive surface area in the environment. Utilizations of NMR-sensitive nuclides within the clay minerals themselves, and in molecules that react with specific sites on the clay mineral surfaces, have aided in understanding the reactivity of these complex aluminosilicate systems.

  5. Raman and infrared spectroscopic study of the mineral goyazite SrAl3(PO4)2(OH)5·H2O

    NASA Astrophysics Data System (ADS)

    López, Andrés; Xi, Yunfei; Frost, Ray L.

    2013-12-01

    We have studied the mineral goyazite using Raman and infrared spectroscopy. Goyazite is a member of the crandallite subgroup of the alunite supergroup. The crystal structure is of the alunite-type and consists of sheets of corner-sharing AlO6 octahedra parallel to (0 0 0 1). The octahedrally coordinated Sr2+ cations occupy cavities between pairs of octahedral sheets and are surrounded by six oxygen atoms from the Al3+O6 octahedra. The very intense sharp band at 983 cm-1 is assigned to the ν1PO43- symmetric stretching mode. The observation of a single band supports the concept that all the phosphate units are equivalent in the structure of goyazite. Raman bands observed at 1029 cm-1 and 1037 cm-1 are assigned to the ν3PO43- antisymmetric stretching vibrations. Two Raman bands at 895 and 927 cm-1 are attributed to the stretching vibrations of H2PO4; thus indicating some hydrogen phosphate units in the structure of goyazite. Raman bands at 556, 581, 596 and 612 cm-1 are assigned to the ν4PO43- bending modes, suggesting a reduction of symmetry of phosphate units. Two sharp Raman bands at 3609 and 3631 cm-1 are attributed to OH stretching vibrations from the goyazite hydroxyl units. Broad Raman bands at 2924, 3043, 3210, 3429 and 3511 cm-1 are assigned to water stretching vibrations. This research shows that from a vibrational spectroscopic point of view, the formula SrAl3(H PO4,PO4)2(OH)6ṡH2O is a better formulation for the mineral goyazite. Vibrational spectroscopy enables subtle details of the molecular structure of goyazite to be determined.

  6. A vibrational spectroscopic study of the phosphate mineral lulzacite Sr2Fe2+(Fe2+,Mg)2Al4(PO4)4(OH)10

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; López, Andrés; Belotti, Fernanda M.; Xi, Yunfei; Scholz, Ricardo

    2014-06-01

    The mineral lulzacite from Saint-Aubin des Chateaux mine, France, with theoretical formula Sr2Fe2+(Fe2+,Mg)2Al4(PO4)4(OH)10 has been studied using a combination of electron microscopy with EDX and vibrational spectroscopic techniques. Chemical analysis shows a Sr, Fe, Al phosphate with minor amounts of Ga, Ba and Mg. Raman spectroscopy identifies an intense band at 990 cm-1 with an additional band at 1011 cm-1. These bands are attributed to the PO43-ν1 symmetric stretching mode. The ν3 antisymmetric stretching modes are observed by a large number of Raman bands. The Raman bands at 1034, 1051, 1058, 1069 and 1084 together with the Raman bands at 1098, 1116, 1133, 1155 and 1174 cm-1 are assigned to the ν3 antisymmetric stretching vibrations of PO43- and the HOPO32- units. The observation of these multiple Raman bands in the symmetric and antisymmetric stretching region gives credence to the concept that both phosphate and hydrogen phosphate units exist in the structure of lulzacite. The series of Raman bands at 567, 582, 601, 644, 661, 673 and 687 cm-1 are assigned to the PO43-ν2 bending modes. The series of Raman bands at 437, 468, 478, 491, 503 cm-1 are attributed to the PO43- and HOPO32-ν4 bending modes. No Raman bands of lulzacite which could be attributed to the hydroxyl stretching unit were observed. Infrared bands at 3511 and 3359 cm-1 are ascribed to the OH stretching vibration of the OH units. Very broad bands at 3022 and 3299 cm-1 are attributed to the OH stretching vibrations of water. Vibrational spectroscopy offers insights into the molecular structure of the phosphate mineral lulzacite.

  7. A vibrational spectroscopic study of the phosphate mineral whiteite CaMn(++)Mg2Al2(PO4)4(OH)2·8(H2O).

    PubMed

    Frost, Ray L; Scholz, Ricardo; López, Andrés; Xi, Yunfei

    2014-04-24

    Vibrational spectroscopy enables subtle details of the molecular structure of whiteite to be determined. Single crystals of a pure phase from a Brazilian pegmatite were used. The infrared and Raman spectroscopy were applied to compare the molecular structure of whiteite with that of other phosphate minerals. The Raman spectrum of whiteite shows an intense band at 972 cm(-1) assigned to the ν1PO4(3-) symmetric stretching vibrations. The low intensity Raman bands at 1076 and 1173 cm(-1) are assigned to the ν3PO4(3-) antisymmetric stretching modes. The Raman bands at 1266, 1334 and 1368 cm(-1) are assigned to AlOH deformation modes. The infrared band at 967 cm(-1) is ascribed to the PO4(3-)ν1 symmetric stretching vibrational mode. The infrared bands at 1024, 1072, 1089 and 1126 cm(-1) are attributed to the PO4(3-)ν3 antisymmetric stretching vibrations. Raman bands at 553, 571 and 586 cm(-1) are assigned to the ν4 out of plane bending modes of the PO4(3-) unit. Raman bands at 432, 457, 479 and 500 cm(-1) are attributed to the ν2 PO4 and H2PO4 bending modes. In the 2600 to 3800 cm(-1) spectral range, Raman bands for whiteite are found 3426, 3496 and 3552 cm(-1) are assigned to AlOH stretching vibrations. Broad infrared bands are also found at 3186 cm(-1). Raman bands at 2939 and 3220 cm(-1) are assigned to water stretching vibrations. Raman spectroscopy complimented with infrared spectroscopy has enabled aspects of the structure of whiteite to be ascertained and compared with that of other phosphate minerals.

  8. Identification of montgomeryite mineral [Ca4MgAl4(PO4)6·(OH)4·12H2O] found in the Jenolan Caves-Australia.

    PubMed

    Frost, Ray L; Xi, Yunfei; Palmer, Sara J; Pogson, Ross E

    2012-08-01

    In this paper, we report on many phosphate containing natural minerals found in the Jenolan Caves - Australia. Such minerals are formed by the reaction of bat guano and clays from the caves. Among these cave minerals is the montgomeryite mineral [Ca(4)MgAl(4)(PO(4))(6)·(OH)(4)·12H(2)O]. The presence of montgomeryite in deposits of the Jenolan Caves - Australia has been identified by X-ray diffraction (XRD). Raman spectroscopy complimented with infrared spectroscopy has been used to characterise the crystal structure of montgomeryite. The Raman spectrum of a standard montgomeryite mineral is identical to that of the Jenolan Caves sample. Bands are assigned to H(2)PO(4)(-), OH and NH stretching vibrations. By using a combination of XRD and Raman spectroscopy, the existence of montgomeryite in the Jenolan Caves - Australia has been proven. A mechanism for the formation of montgomeryite is proposed.

  9. Raman and infrared spectroscopic characterization of the phosphate mineral paravauxite Fe2+Al2(PO4)2(OH)2ṡ8H2O

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; Scholz, Ricardo; Lópes, Andrés; Xi, Yunfei; Gobac, Željka Žigovečki; Horta, Laura Frota Campos

    2013-12-01

    We have undertaken a vibrational spectroscopic study of paravauxite the Siglo XX mine, Bustillo Province, northern of Potosí department, Bolivia. This mine is important source for rare and unusual secondary phosphate minerals and is the type locality for a number of rare phosphates such as vauxite, sigloite, metavauxite and for jeanbandyite. The chemical formula of the studied sample was determined as Fe0.952+,(Al0.07)Σ1.02(Al)2.09(PO4)1.97(OH)1.98·7.90(H2O). The Raman spectrum is dominated by an intense Raman band at 1020 cm-1 assigned to the PO43-ν1 symmetric stretching mode. Low intensity Raman bands found at 1058, 1115 and 1148 cm-1 are assigned to the PO43-ν3 antisymmetric stretching vibrations. Raman bands of paravauxite at 537, 570, 609 and 643 cm-1 are assigned to the ν4PO43- bending modes whilst the Raman bands at 393 and 420 cm-1 are due to the ν2PO43- bending modes. The Raman spectral profile of paravauxite in the hydroxyl stretching region is broad with component bands resolved at 3086, 3215, 3315, 3421, 3505 and 3648 cm-1. Vibrational spectroscopy enables the assessment of the molecular structure of paravauxite to be undertaken.

  10. Nevadaite, (Cu2+, Al, V3+)6 [Al8 (PO4)8 F8] (OH 2 (H2O)22, a new phosphate mineral species from the Gold Quarry mine, Carlin, Eureka County, Nevada: description and crystal structure

    USGS Publications Warehouse

    Cooper, M.A.; Hawthorne, F.C.; Roberts, Andrew C.; Foord, E.E.; Erd, Richard C.; Evans, H.T.; Jensen, M.C.

    2004-01-01

    Nevadaite, (Cu2+, ???, Al, V3+)6 (PO4)8 F8 (OH)2 (H2O)22, is a new supergene mineral species from the Gold Quarry mine, near Carlin, Eureka County, Nevada, U.S.A. Nevadaite forms radiating clusters to 1 mm of prismatic crystals, locally covering surfaces more that 2 cm across; individual crystals are elongate on [001] with a length:width ratio of > 10:1 and a maximum diameter of ???30 ??m. It also occurs as spherules and druses associated with colorless to purple-black fluellite, colorless wavellite, strengitevariscite, acicular maroon-to-red hewettite, and rare anatase, kazakhstanite, tinticite, leucophosphite, torbernite and tyuyamunite. Nevadaite is pale green to turquoise blue with a pale powder-blue streak and a vitreous luster; it does not fluoresce under ultra-violet light. It has no cleavage, a Mohs hardness of ???3, is brittle with a conchoidal fracture, and has measured and calculated densities of 2.54 and 2.55 g/cm3, respectively. Nevadaite is biaxial negative, with ?? 1.540, ?? 1.548, ?? 1.553, 2V(obs.) = 76??, 2V(calc.) = 76??, pleochroic with X pale greenish blue, Y very pale greenish blue, Z blue, and with absorption Z ??? X > Y and orientation X = c, Y = a, Z = b. Nevadaite is orthorhombic, space group P21mn, a 12.123(2), b 18.999(2), c 4.961(1) A?? , V 1142.8(2) A??3, Z = 1, a:b:c = 0.6391:1:0.2611. The strongest seven lines in the X-ray powder-diffraction pattern [d in A??(I)(hkl)] are: 6.077(10)(200), 5.618(9)(130), 9.535(8)(020), 2.983(6)(241), 3.430(4)(041), 2.661(4)(061 , and 1.844(4)(352). A chemical analysis with an electron microprobe gave P2O5 32.54, Al2O3 27.07, V2O3 4.24, Fe2O3 0.07, CuO 9.24, ZnO 0.11, F 9.22, H2O (calc.) 23.48, OH ??? F -3.88, sum 102.09 wt.%; the valence states of V and Fe, and the amount of H2O, were determined by crystal-structure analysis. The resulting empirical formula on the basis of 63.65 anions (including 21.65 H2O pfu) is (CU2+2.00 Zn0.02 V3+0.98 Fe3+0.01 Al1.15)??4.16 Al8 P7.90 O32 [F8.37 (OH 1.63]??10 (H2O

  11. Vibrational spectroscopy of the phosphate mineral lazulite--(Mg, Fe)Al2(PO4)2·(OH)2 found in the Minas Gerais, Brazil.

    PubMed

    Frost, Ray L; Xi, Yunfei; Beganovic, Martina; Belotti, Fernanda Maria; Scholz, Ricardo

    2013-04-15

    This research was done on lazulite samples from the Gentil mine, a lithium bearing pegmatite located in the municipality of Mendes Pimentel, Minas Gerais, Brazil. Chemical analysis was carried out by electron microprobe analysis and indicated a magnesium rich phase with partial substitution of iron. Traces of Ca and Mn, (which partially replaced Mg) were found. The calculated chemical formula of the studied sample is: (Mg0.88, Fe0.11)Al1.87(PO4)2.08(OH)2.02. The Raman spectrum of lazulite is dominated by an intense sharp band at 1060 cm(-1) assigned to PO stretching vibrations of of tetrahedral [PO4] clusters presents into the HPO4(2-) units. Two Raman bands at 1102 and 1137 cm(-1) are attributed to both the HOP and PO antisymmetric stretching vibrations. The two infrared bands at 997 and 1007 cm(-1) are attributed to the ν1PO4(3-) symmetric stretching modes. The intense bands at 1035, 1054, 1081, 1118 and 1154 cm(-1) are assigned to the ν3PO4(3-) antisymmetric stretching modes from both the HOP and tetrahedral [PO4] clusters. A set of Raman bands at 605, 613, 633 and 648 cm(-1) are assigned to the ν4 out of plane bending modes of the PO4, HPO4 and H2PO4 units. Raman bands observed at 414, 425, 460, and 479 cm(-1) are attributed to the ν2 tetrahedral PO4 clusters, HPO4 and H2PO4 bending modes. The intense Raman band at 3402 and the infrared band at 3403 cm(-1) are assigned to the stretching vibration of the OH units. A combination of Raman and infrared spectroscopy enabled aspects of the molecular structure of the mineral lazulite to be understood.

  12. Application of the Ti-in-quartz thermobarometer to rutile-free systems. Reply to: a comment on: `TitaniQ under pressure: the effect of pressure and temperature on the solubility of Ti in quartz' by Thomas et al.

    NASA Astrophysics Data System (ADS)

    Thomas, Jay B.; Bruce Watson, E.

    2012-08-01

    The premise of the Wilson et al. comment is that the Ti-in-quartz solubility calibration (Thomas et al. in Contrib Mineral Petrol 160:743-759, 2010) is fundamentally flawed. They reach this conclusion because P- T estimates using the Ti-in-quartz calibration differ from their previous interpretations for crystallization conditions of the Bishop and Oruanui rhyolites. If correct, this assertion has far-reaching implications, so a careful assessment of the Wilson et al. reasoning is warranted. Application of the Ti-in-quartz calibration as a thermobarometer in rutile-free rocks requires an estimation of TiO2 activity in the liquid ( a_{{{{TiO}}_{ 2} }} (liquid-rutile); referenced to rutile saturation) and an independent constraint on either P or T to obtain the crystallization temperature or pressure, respectively. The foundation of Wilson et al.'s argument is that temperature estimates obtained from Fe-Ti oxide thermometry accurately reflect crystallization conditions of quartz in the two rhyolites discussed. We maintain that our experimental approach is sound, the thermodynamic basis of the Ti-in-quartz calibration is fundamentally correct, and our experimental results are robust and reproducible. We suggest that the reason Wilson et al. obtain implausible pressure estimates is because estimates for T and a_{{{{TiO}}_{ 2} }} they used as input values for the Ti-in-quartz calibration are demonstrably too high. Numerous studies show that Fe-Ti oxide temperature estimates of some rhyolites are substantially higher than those predicted by well-constrained phase equilibria. In this reply, we show that when reasonable input values for T and a_{{{{TiO}}_{ 2} }} (liquid-rutile) are used, pressure estimates obtained from the Ti-in-quartz calibration are well aligned with phase equilibria and essentially identical to melt inclusion volatile saturation pressures.

  13. Experimental constraints on mineral-melt reactions in the Middle Zone of the Skaergaard intrusion

    NASA Astrophysics Data System (ADS)

    Veksler, I. V.; Nielsen, T. F.

    2009-12-01

    The Eocene Skaergaard intrusion (East Greenland) is the classical example of the Fe enrichment trend in tholeitic magma. Despite numerous attempts to reproduce the trend experimentally, its direction in the Middle Zone (MZ) of the intrusion remains contentious. It remains unclear whether the strong Fe enrichment of the magma continued after the start of ilmenite and magnetite crystallization. Thy et al. (2009) recently showed that the modal ratio of Fe-Ti oxide minerals to Fe-Mg silicates in average Skaergaard rocks was lower than the experimentally determined cotectic proportions. In our view, the difference probably resulted from mineral-melt post-cumulus reactions. Cumulus assemblage in the MZ comprised plagioclase, high- and low-Ca pyroxenes, ilmenite and magnetite. Olivine is locally present as an inter-cumulus phase. All the minerals and the liquid were involved in continuous and discontinuous reaction series. Traces of the reactions are ubiquitous throughout the intrusion, and especially prominent around autolithic blocks (Irvine et al., 1998; McBirney, 2009). We examined experimental constraints on the reactions from 67 experimental equilibria compiled from 25 publications, in which dry silicate melts coexisted with plagioclase, olivine, and two pyroxenes. The experiments had been carried out at 1 atm, temperatures between 1040 and 1180 °C, and variable fO2. We found that the 4-mineral assemblage did not constrain a narrow range of liquid compositions. For example, SiO2 in the liquids varies broadly from 42 to 66 wt.%. Cotectic proportions of the crystal phases vary accordingly. FeO and alkalis impose strong and opposite effects on the cotectic proportions and equilibrium melt compositions. Thus, alkali-poor liquids evolve to FeO concentrations of up to 30 wt. %. We propose that the mineral-melt reactions compounded by migration of FeO and alkalis in the liquid may explain poorly understood phenomena such as the reverse evolution of plagioclase towards

  14. Enthalpies of formation of low albite (NaAlSi3O8), gibbsite (Al(OH)3), and NaAlO2; revised values for ΔH°f,298 and ΔG°f,298 of some aluminosilicate minerals

    USGS Publications Warehouse

    Hemingway, Bruce S.; Robie, Richard A.

    1977-01-01

    The enthalpies of formation from the elements ΔH°t, of low albite, analbite, NaAlSi3O8 glass, gibbsite (Al(OH)3), and NaAlO2, have been determined by hydrofluoric acid solution calorimetry from measurements of the heats of solution, ΔH°soln, of low albite, NaAlO2, SiO2, Al(OH)3, Al, H2O, NaCl, and HC1-12.731H2O in 20.1 weight percent HF(aq) at temperatures between 303.15 and 348.15 K. At 298.15 K the enthalpies of formation, ΔH°f,298, for low albite, analbite, NaAlSi3O8 glass, gibbsite (Al(OH)3), and NaAlO2 are -3 935 115±3415, -3 924 235±3640, -3 875 455±3700, ±1293130±1190, and 1135 990±1255 J mol-1, respectively. Our values for the enthalpies of formation of low albite, analbite, and for NaAlSi3O8 glass are approximately 13 810 J mol-1 more negative than the values calculated by D. R. Waldbaum in 1968. Our value for the enthalpy of formation of gibbsite at 298.15 K is 11234 J more negative than the value of R. Barany and K. K. Kelley obtained in 1961. The standard Gibbs free energies of formation, ΔG°f,298 for low albite, analbite, and gibbsite calculated from the above enthalpies and the appropriate entropy data are -3 711 715±3435, -3 706 500±3660, and -1154 890±1200 J mol-1, respectively. The enthalpy of solution of Standard Reference Material 1654, α-quartz (37 to 74 μm), in 20.1 wt percent HF(aq) is -137 737±209 J mol-1 at 333.15 K. This value is approximately 1255 J less negative than the value obtained by King in 1951 and 1952 for material that has a mean particle diameter of less than 5 μm and that has been used by the U.S. Bureau of Mines in their determinations of the enthalpies of formation of many silicates. Revised values of the enthalpies and Gibbs free energies of formation are presented for some aluminosilicate minerals, based upon this new data for ΔH°f,298 of gibbsite and the heat of solution of α-quartz.

  15. Reply to Comment by Xu et al. on "Sr-Nd isotope composition and clay mineral assemblages in eolian dust from the central Philippine Sea over the last 600 kyr: Implications for the transport mechanism of Asian dust" by Seo et al.

    NASA Astrophysics Data System (ADS)

    Seo, Inah; Lee, Yong Il; Yoo, Chan Min; Kim, Hyung Jeek; Hyeong, Kiseong

    2016-12-01

    Against Xu et al. (2016), who argued that East Asian Desert (EAD) dust that traveled on East Asian Winter Monsoon winds dominates over Central Asian Desert (CAD) dust in the Philippine Sea with presentation of additional data, we reconfirm Seo et al.'s (2014) conclusion that CAD dust carried on the Prevailing Westerlies and Trade Winds dominates over EAD dust in overall dust budget of the central Philippine Sea. The relative contribution of dust from EADs and CADs using clay mineral composition should be evaluated with elimination of mineralogical contribution from the volcanic end-member which is enriched in kaolinite and overestimate the contribution of EAD dust.

  16. Experimental transport of Si, Al and Mg in hydrothermal solutions: an application to vein mineralization during high-pressure, low-temperature metamorphism in the French Alps

    NASA Astrophysics Data System (ADS)

    Goffé, Bruno; Murphy, William M.; Lagache, Martine

    1987-12-01

    A study of hydrothermal vein mineralization in meta-argillites subjected to high-pressure, low-temperature metamorphism reveals that ferromagnesian (e.g., chlorite) and pure aluminosilicate (e.g., pyrophyllite) mineralization can be correlated with regimes of increasing and decreasing temperature, respectively. An experimental study of the transport of silica, aluminum and magnesium in hydrothermal solutions has been undertaken to simulate variations in the physical conditions during metamorphism and the accompanying mass transport in a closed system. Thermodynamic and kinetic analysis of the experimental results indicates that local equilibrium among aqueous and mineral phases controls the distribution and composition of hydrothermal vein mineralization and that vein mineralogy can be used to infer the sense of variation of pressure and temperature during metamorphism.

  17. Mineral oils

    NASA Technical Reports Server (NTRS)

    Furby, N. W.

    1973-01-01

    The characteristics of lubricants made from mineral oils are discussed. Types and compositions of base stocks are reviewed and the product demands and compositions of typical products are outlined. Processes for commercial production of mineral oils are examined. Tables of data are included to show examples of product types and requirements. A chemical analysis of three types of mineral oils is reported.

  18. Vladimirivanovite, Na6Ca2[Al6Si6O24](SO4,S3,S2,Cl)2 · H2O, a new mineral of sodalite group

    NASA Astrophysics Data System (ADS)

    Sapozhnikov, A. N.; Kaneva, E. V.; Cherepanov, D. I.; Suvorova, L. F.; Levitsky, V. I.; Ivanova, L. A.; Reznitsky, L. Z.

    2012-12-01

    The results of an examination of vladimirivanovite, a new mineral of the sodalite group, found at the Tultui deposit in the Baikal region are discussed. The mineral occurs in the form of outer rims (0.01-3 mm thick) of lazurite, elongated segregations without faced crystals (0.2 to 3-4 mm in size; less frequently, 4 × 12-15 × 20 mm), and rare veinlets (up to 5 mm) hosted in calciphyre and marble. Vladimirivanovite is irregular and patchy dark blue. The mineral is brittle; on average, the microhardness VHN is 522-604, 575 kg/mm2; and the Mohs hardness is 5.0-5.5. The measured and calculated densities are 2.48(3) and 2.436 g/cm3, respectively. Vladimirivanovite is optically biaxial; 2 V meas = 63(±1)°, 2 V calc = 66.2°; the refractive indices are α = 1.502-1.507 (±0.002), N m = 1.509-1.514 (±0.002), and N g = 1.512-1.517 (±0.002). The chemical composition is as follows, wt %: 32.59 SiO2, 27.39 Al2O3, 7.66 CaO, 17.74 Na2O, 11.37 SO3, 1.94 S, 0.12 Cl, and 1.0 H2O; total is 99.62. The empirical formula calculated based on (Si + Al) = 12 with sulfide sulfur determined from the charge balance is Na6.36Ca1.52(Si6.03Al5.97)Σ12O23.99(SO4)1.58(S3)0.17(S2)0.08 · Cl0.04 · 0.62H2O; the idealized formula is Na6Ca2[Al6Si6O24](SO4,S3,S2,Cl)2 · H2O. The new mineral is orthorhombic, space group Pnaa; the unit-cell dimensions are a = 9.066, b = 12.851, c = 38.558 Å, V = 4492 Å3, and Z = 6. The strongest reflections in the X-ray powder diffraction pattern ( dÅ— I[ hkl]) are: 6.61-5[015], 6.43-11[020, 006], 3.71-100[119, 133], 2.623-30[20.12, 240], 2.273-6[04.12], 2.141-14[159, 13.15], 1.783-9[06.12, 04.18], and 1.606-6[080, 00.24]. The crystal structure has been solved with a single crystal. The mineral was named in memoriam of Vladimir Georgievich Ivanov (1947-2002), Russian mineralogist and geochemist. The type material of the mineral is deposited at the Mineralogical Museum of St. Petersburg State University, St. Petersburg, Russia.

  19. Vibrational spectroscopic study of the sulphate mineral glaucocerinite (Zn,Cu)10Al6(SO4)3(OH)32ṡ18H2O - A natural layered double hydroxide

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; Theiss, Frederick L.; López, Andrés; Scholz, Ricardo

    2014-06-01

    We have studied the molecular structure of the mineral glaucocerinite (Zn,Cu)5Al3(SO4)1.5(OH)16ṡ9(H2O) using a combination of Raman and infrared spectroscopy. The mineral is one of the hydrotalcite supergroup of natural layered double hydroxides. The Raman spectrum is characterised by an intense Raman band at 982 cm-1 with a low intensity band at 1083 cm-1. These bands are attributed to the sulphate symmetric and antisymmetric stretching mode. The infrared spectrum is quite broad with a peak at 1020 cm-1. A series of Raman bands at 546, 584, 602, 625 and 651 cm-1 are assigned to the ν4 (SO4)2- bending modes. The observation of multiple bands provides evidence for the reduction in symmetry of the sulphate anion from Td to C2v or even lower symmetry. The Raman band at 762 cm-1 is attributed to a hydroxyl deformation mode associated with AlOH units. Vibrational spectroscopy enables aspects of the molecular structure of glaucocerinite to be determined.

  20. Microbially mediated mineral carbonation

    NASA Astrophysics Data System (ADS)

    Power, I. M.; Wilson, S. A.; Dipple, G. M.; Southam, G.

    2010-12-01

    Mineral carbonation involves silicate dissolution and carbonate precipitation, which are both natural processes that microorganisms are able to mediate in near surface environments (Ferris et al., 1994; Eq. 1). (Ca,Mg)SiO3 + 2H2CO3 + H2O → (Ca,Mg)CO3 + H2O + H4SiO4 + O2 (1) Cyanobacteria are photoautotrophs with cell surface characteristics and metabolic processes involving inorganic carbon that can induce carbonate precipitation. This occurs partly by concentrating cations within their net-negative cell envelope and through the alkalinization of their microenvironment (Thompson & Ferris, 1990). Regions with mafic and ultramafic bedrock, such as near Atlin, British Columbia, Canada, represent the best potential sources of feedstocks for mineral carbonation. The hydromagnesite playas near Atlin are a natural biogeochemical model for the carbonation of magnesium silicate minerals (Power et al., 2009). Field-based studies at Atlin and corroborating laboratory experiments demonstrate the ability of a microbial consortium dominated by filamentous cyanobacteria to induce the precipitation of carbonate minerals. Phototrophic microbes, such as cyanobacteria, have been proposed as a means for producing biodiesel and other value added products because of their efficiency as solar collectors and low requirement for valuable, cultivable land in comparison to crops (Dismukes et al., 2008). Carbonate precipitation and biomass production could be facilitated using specifically designed ponds to collect waters rich in dissolved cations (e.g., Mg2+ and Ca2+), which would allow for evapoconcentration and provide an appropriate environment for growth of cyanobacteria. Microbially mediated carbonate precipitation does not require large quantities of energy or chemicals needed for industrial systems that have been proposed for rapid carbon capture and storage via mineral carbonation (e.g., Lackner et al., 1995). Therefore, this biogeochemical approach may represent a readily

  1. Alloriite, Na5K1.5Ca(Si6Al6O24)(SO4)(OH)0.5 · H2O, a new mineral species of the cancrinite group

    NASA Astrophysics Data System (ADS)

    Chukanov, N. V.; Rastsvetaeva, R. K.; Pekov, I. V.; Zadov, A. E.

    2007-12-01

    Alloriite, a new mineral species, has been found in volcanic ejecta at Mt. Cavalluccio (Campagnano municipality, Roma province, Latium region, Italy) together with sanidine, biotite, andradite, and apatite. The mineral is named in honor of Roberto Allori (b. 1933), an amateur mineralogist and prominent mineral collector who carried out extensive and detailed field mineralogical investigations of volcanoes in the Latium region. Alloriite occurs as short prismatic and tabular crystals up to 1.5 × 2 mm in size. The mineral is colorless, transparent, with a white streak and vitreous luster. Alloriite is not fluorescent and brittle; the Mohs’ hardness is 5. The cleavage is imperfect parallel to {10overline 1 0}. The density measured with equilibration in heavy liquids is 2.35g/cm3 and calculated density ( D calc) is 2.358 g/cm3 (on the basis of X-ray single-crystal data) and 2.333 g/cm3 (from X-ray powder data). Alloriite is optically uniaxial, positive, ω = 1.497(2), and ɛ = 1.499(2). The infrared spectrum is given. The chemical composition (electron microprobe, H2O determined using the Penfield method, CO2, with selective sorption, wt %) is: 13.55 Na2O, 6.67 K2O, 6.23 CaO, 26.45 Al2O3, 34.64 SiO2, 8.92 SO3, 0.37 Cl, 2.1 H2O, 0.7 CO2, 0.08-O = Cl2, where the total is 99.55. The empirical formula ( Z = 1) is Na19.16K6.21Ca4.87(Si25.26Al22.74O96)(SO4)4.88(CO3)0.70Cl0.46(OH)0.76 · 4.73H2O. The simplified formula (taking into account the structural data, Z = 4) is: [Na(H2O)][Na4K1.5(SO4)] · [Ca(OH,Cl)0.5](Si6Al6O24). The crystal structure has been studied ( R = 0.052). Alloriite is trigonal, the space group is P31 c; the unit-cell dimensions are a = 12.892(3), c = 21.340(5) Å, and V = 3071.6(15) Å3. The crystal structure of alloriite is based on the same tetrahedral framework as that of afghanite. In contrast to afghanite containing clusters [Ca-Cl]+ and chains ...Ca-Cl-Ca-Cl..., the new mineral contains clusters [Na-H2O]+ and chains ...Na-H2O-Na-H2O.... The

  2. A vibrational spectroscopic study of the silicate mineral harmotome--(Ba,Na,K)1-2(Si,Al)8O16⋅6H2O--a natural zeolite.

    PubMed

    Frost, Ray L; López, Andrés; Wang, Lina; Romano, Antônio Wilson; Scholz, Ricardo

    2015-02-25

    The mineral harmotome (Ba,Na,K)1-2(Si,Al)8O16⋅6H2O is a crystalline sodium calcium silicate which has the potential to be used in plaster boards and other industrial applications. It is a natural zeolite with catalytic potential. Raman bands at 1020 and 1102 cm(-1) are assigned to the SiO stretching vibrations of three dimensional siloxane units. Raman bands at 428, 470 and 491 cm(-1) are assigned to OSiO bending modes. The broad Raman bands at around 699, 728, 768 cm(-1) are attributed to water librational modes. Intense Raman bands in the 3100 to 3800 cm(-1) spectral range are assigned to OH stretching vibrations of water in harmotome. Infrared spectra are in harmony with the Raman spectra. A sharp infrared band at 3731 cm(-1) is assigned to the OH stretching vibration of SiOH units. Raman spectroscopy with complimentary infrared spectroscopy enables the characterization of the silicate mineral harmotome.

  3. A vibrational spectroscopic study of the silicate mineral harmotome - (Ba,Na,K)1-2(Si,Al)8O16ṡ6H2O - A natural zeolite

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; López, Andrés; Wang, Lina; Romano, Antônio Wilson; Scholz, Ricardo

    2015-02-01

    The mineral harmotome (Ba,Na,K)1-2(Si,Al)8O16ṡ6H2O is a crystalline sodium calcium silicate which has the potential to be used in plaster boards and other industrial applications. It is a natural zeolite with catalytic potential. Raman bands at 1020 and 1102 cm-1 are assigned to the SiO stretching vibrations of three dimensional siloxane units. Raman bands at 428, 470 and 491 cm-1 are assigned to OSiO bending modes. The broad Raman bands at around 699, 728, 768 cm-1 are attributed to water librational modes. Intense Raman bands in the 3100 to 3800 cm-1 spectral range are assigned to OH stretching vibrations of water in harmotome. Infrared spectra are in harmony with the Raman spectra. A sharp infrared band at 3731 cm-1 is assigned to the OH stretching vibration of SiOH units. Raman spectroscopy with complimentary infrared spectroscopy enables the characterization of the silicate mineral harmotome.

  4. Sb(III) and Sb(V) Sorption onto Al-Rich Phases: Hydrous Al Oxide and the Clay Minerals Kaolinite KGa-1b and Oxidized and Reduced Nontronite NAu-1

    SciTech Connect

    Ilgen, Anastasia G.; Trainor, Thomas P.

    2012-11-13

    We have studied the immobilization of Sb(III) and Sb(V) by Al-rich phases - hydrous Al oxide (HAO), kaolinite (KGa-1b), and oxidized and reduced nontronite (NAu-1) - using batch experiments to determine the uptake capacity and the kinetics of adsorption and Extended X-ray Absorption Fine Structure (EXAFS) Spectroscopy to characterize the molecular environment of adsorbed Sb. Both Sb(III) and Sb(V) are adsorbed in an inner-sphere mode on the surfaces of the studied substrates. The observed adsorption geometry is mostly bidentate corner-sharing, with some monodentate complexes. The kinetics of adsorption is relatively slow (on the order of days), and equilibrium adsorption isotherms are best fit using the Freundlich model. The oxidation state of the structural Fe within nontronite affects the adsorption capacity: if the clay is reduced, the adsorption capacity of Sb(III) is slightly decreased, while Sb(V) uptake is increased significantly. This may be a result of the presence of dissolved Fe(II) in the reduced nontronite suspensions or associated with the structural rearrangements in nontronite due to reduction. These research findings indicate that Sb can be effectively immobilized by Al-rich phases. The increase in Sb(V) uptake in response to reducing structural Fe in clay can be important in natural settings since Fe-rich clays commonly go through oxidation-reduction cycles in response to changing redox conditions.

  5. Esperanzaite, NaCa2Al2(As5+O4)2F4(OH)*2H2O, a new mineral species from the La Esperanza mine, Mexico: descriptive mineralogy and atomic arrangement

    USGS Publications Warehouse

    Foord, E.E.; Hughes, J.M.; Cureton, F.; Maxwell, C.H.; Falster, A.U.; Sommer, A.J.; Hlava, P.F.

    1999-01-01

    Esperanzaite, ideally NaCa2Al2(As5+O4)2F4(OH)??2H2O, Z = 2, is a new mineral species from the La Esperanza mine, Durango State, Mexico. The mineral occurs as blue-green botryoidal crystalline masses on rhyolite, with separate spheres up to 1.5 mm in diameter. The Mohs hardness is 4 1/2 , and the specific gravity, 3.24 (obs.) and 3.36(3) (calc.). Optical properties were measured in 589 nm light. Esperanzaite is biaxial (-), X = Y = Z = colorless, ?? 1.580(1), ?? 1.588(1), and ?? 1.593(1); 2V(obs) is 74(1)??and 2V(calc) is 76.3??. The dispersion is medium, r < v, and the optic axes are oriented according to a ?? Z = +50.5??, b = Y, c ?? X = +35??. The strongest five X-ray-diffraction maxima in the powder pattern [d in A??(I)(hkl)] are: 2.966(100)(131, 311, 031), 3.527(90)(220), 2.700(90)(221,002,040), 5.364(80)(001,020) and 4.796(80)(011). Esperanzaite is monoclinic, a 9.687(5), b 10.7379(6), c 5.5523(7) A??, ?? 105.32(1)??, space group P21/m. The atomic arrangement of esperanzaite was solved by direct methods and Fourier analysis (R = 0.032). The Fundamental Building Block (FBB) is formed of [001] stacks of heteropolyhedral tetramers; the tetramers are formed of two arsenate tetrahedra and two Al octahedra, corner-linked in four-member rings. The FBBs are linked by irregular Na??5 and Ca??8 polyhedra.

  6. Lunar highland rocks - Element partitioning among minerals. II - Electron microprobe analyses of Al, P, Ca, Ti, Cr, Mn and Fe in olivine

    NASA Technical Reports Server (NTRS)

    Smith, J. V.; Hansen, E. C.; Steele, I. M.

    1980-01-01

    Lunar olivines from anorthosites, granulitic impactites, and rocks in the Mg-rich plutonic trend were subjected to electron probe measurements for Al, P, Ca, Ti, Cr and Mn, which show that the FeO/MnO ratio for lunar olivines lies between 80 and 110 with little difference among the rock types. The low values of Ca in lunar olivines indicate slow cooling to subsolidus temperatures, with blocking temperatures of about 750 C for 67667 and 1000 C for 60255,73-alpha determined by the Finnerty and Boyd (1978) experiments. An important paradox is noted in the low Ti content of Fe-rich olivines from anorthosites, although both Ti and Fe tend to become enriched in liquid during fractional distillation. Except for Ca and Mn, olivine from anorthosites has lower minor element values than other rock types. Formation from a chemically distinct system is therefore implied.

  7. Esperanzaite, NaCa(2)Al(2)(As(5+)O(4))[As(5+)O(3)(OH)](OH)(2)F(4)(H(2)O), A New Mineral From Mina La Esperanza, Mexico: Descriptive Mineralogy and Atomic Arrangement

    SciTech Connect

    Cureton, F.; Falster, A.U.; Foord, E.E.; Hlava, P.F.; Hughes, J.M.; Maxwell, C.H.

    1998-11-09

    Esperanzaite, ideally NaCazA12(As5+0.i)[As5+03 (OH)] (OH)2FJH20), Z =2, is a new mineral from the Mina h Esperarq Durango State, Mexico. The mineral occurs as blue-green botryoidal crystalline masses on rhyolite, with separate spheres up to 1.5 mm Y Deceased in diameter. Mobs hardness is 4.5, specific gravity 3.240h, and 3.36( 3)C.IC. Optical properties were measured in 589 nm light. Esperanzaite is biaxial (-), .Y= Y = Z= colorless, a 1.580(1), ~ 1.588( 1), and y 1.593(1 ); 2V0hs is 74(1 ~ and 2 }'CUIC is 76.3". Dispersion is medium, r < v, and optic axes are oriented as a A Z = +50.5o, b = Y, c P. X = +35". The five strongest X-ray diffraction maxima in the powder pattern are (~ /, hk~: 2.966,100, 13 i, 31 i, 031 ; 3.527,90, 220; 2.700,90,221,002, 040; 5.364>80, 001, 020; 4.796,80,011. Esperanzaite is monoclinic, u 9.687(5), b 10.7379(6), c 5.5523(7)& ~ 105.32( 1 )", space group P21/nz. The atomic arrangement of esperanzaite was solved by Direct Methods and Fourier analysis (R= 0.03 1). The Fundamental Building Block is formed of stacks of heteropolyhedral tetramers; the tetramers are formed of two arsenate tetrahedral and two Al octahedra, comer-linked in 4-member rings. The Fundamental Building Blocks are linked by irregular lda~j and Ca@ polyhedra.

  8. Industrial Minerals

    ERIC Educational Resources Information Center

    Bradbury, James C.

    1978-01-01

    The past year is seen as not particularly good for industrial minerals and for industry in general. Environmental concerns continued to trouble the industry with unacceptable asbestos concentrations and chlorofluorocarbon effects on ozone. A halting U.S. economy also affected industrial progress. (MA)

  9. Thermodynamic modeling of non-ideal mineral-fluid equilibria in the system Si-Al-Fe-Mg-Ca-Na-K-H-O-Cl at elevated temperatures and pressures: Implications for hydrothermal mass transfer in granitic rocks

    NASA Astrophysics Data System (ADS)

    Dolejš, David; Wagner, Thomas

    2008-01-01

    We present the results of thermodynamic modeling of fluid-rock interaction in the system Si-Al-Fe-Mg-Ca-Na-H-O-Cl using the GEM-Selektor Gibbs free energy minimization code. Combination of non-ideal mixing properties in solids with multicomponent aqueous fluids represents a substantial improvement and it provides increased accuracy over existing modeling strategies. Application to the 10-component system allows us to link fluid composition and speciation with whole-rock mineralogy, mass and volume changes. We have simulated granite-fluid interaction over a wide range of conditions (200-600 °C, 100 MPa, 0-5 m Cl and fluid/rock ratios of 10-2-104) in order to explore composition of magmatic fluids of variable salinity, temperature effects on fluid composition and speciation and to simulate several paths of alteration zoning. At low fluid/rock ratios (f/r) the fluid composition is buffered by the silicate-oxide assemblage and remains close to invariant. This behavior extends to a f/r of 0.1 which exceeds the amount of exsolved magmatic fluids controlled by water solubility in silicate melts. With increasing peraluminosity of the parental granite, the Na-, K- and Fe-bearing fluids become more acidic and the oxidation state increases as a consequence of hydrogen and ferrous iron transfer to the fluid. With decreasing temperature, saline fluids become more Ca- and Na-rich, change from weakly acidic to alkaline, and become significantly more oxidizing. Large variations in Ca/Fe and Ca/Mg ratios in the fluid are a potential geothermometer. The mineral assemblage changes from cordierite-biotite granites through two-mica granites to chlorite-, epidote- and zeolite-bearing rocks. We have carried out three rock-titration simulations: (1) reaction with the 2 m NaCl fluid leads to albitization, chloritization and desilication, reproducing essential features observed in episyenites, (2) infiltration of a high-temperature fluid into the granite at 400 °C leads to hydrolytic

  10. Mineral bioprocessing

    SciTech Connect

    Torma, A.E.

    1993-05-01

    In the last 25 years, the introduction of biotechnological methods in hydrometallurgy has created new opportunities and challenges for the mineral processing industry. This was especially true for the production of metal values from mining wastes and low-and-complex-grade mineral resources, which were considered economically not amenable for processing by conventional extraction methods. Using bio-assisted heap, dump and in-situ leaching technologies, copper and uranium extractions gained their first industrial applications. The precious metal industries were the next to adopt the bio-preoxidation technique in the extraction of gold from refractory sulfide-bearing ores and concentrates. A variety of other bioleaching opportunities exist for nickel, cobalt, cadmium and zinc sulfide leaching. Recently developed bioremediation methods and biosorption technologies have shown a good potential for industrial applications to remove trace heavy metal and radionuclide concentrations from contaminated soils, and mining and processing effluents.

  11. Biachellaite, (Na,Ca,K)8(Si6Al6O24)(SO4)2(OH)0.5 · H2O, a new mineral species of the cancrinite group

    NASA Astrophysics Data System (ADS)

    Chukanov, N. V.; Rastsvetaeva, R. K.; Pekov, I. V.; Zadov, A. E.; Allori, R.; Zubkova, N. V.; Giester, G.; Puscharovsky, D. Yu.; van, K. V.

    2009-12-01

    Biachellaite, a new mineral species of the cancrinite group, has been found in a volcanic ejecta in the Biachella Valley, Sacrofano Caldera, Latium region, Italy, as colorless isometric hexagonal bipyramidal-pinacoidal crystals up to 1 cm in size overgrowing the walls of cavities in a rock sample composed of sanidine, diopside, andradite, leucite and hauyne. The mineral is brittle, with perfect cleavage parallel to {10 bar 1 0} and imperfect cleavage or parting (?) parallel to {0001}. The Mohs hardness is 5. Dmeas = 2.51(1) g/cm3 (by equilibration with heavy liquids). The densities calculated from single-crystal X-ray data and from X-ray powder data are 2.515 g/cm3 and 2.520 g/cm3, respectively. The IR spectrum demonstrates the presence of SO{4/2-}, H2O, and absence of CO{3/2-}. Biachellaite is uniaxial, positive, ω = 1.512(1), ɛ = 1.514(1). The weight loss on ignition (vacuum, 800°C, 1 h) is 1.6(1)%. The chemical composition determined by electron microprobe is as follows, wt %: 10.06 Na2O, 5.85 K2O, 12.13 CaO, 26.17 Al2O3, 31.46 SiO2, 12.71 SO3, 0.45 Cl, 1.6 H2O (by TG data), -0.10 -O=Cl2, total is 100.33. The empirical formula ( Z = 15) is (Na3.76Ca2.50K1.44)Σ7.70(Si6.06Al5.94O24)(SO4)1.84Cl0.15(OH)0.43 · 0.81H2O. The simplified formula is as follows: (Na,Ca,K)8(Si6Al6O24)(SO4)2(OH)0.5 · H2O. Biachellaite is trigonal, space group P3, a =12.913(1), c = 79.605(5) Å; V = 11495(1) Å3. The crystal structure of biachellaite is characterized by the 30-layer stacking sequence ( ABCABCACACBACBACBCACBACBACBABC)∞. The tetrahedral framework contains three types of channels composed of cages of four varieties: cancrinite, sodalite, bystrite (losod) and liottite. The strongest lines of the X-ray powder diffraction pattern [ d, Å ( I, %) ( hkl)] are as follows: 11.07 (19) (100, 101), 6.45 (18) (110, 111), 3.720 (100) (2.1.10, 300, 301, 2.0.16, 302), 3.576 (18) (1.0.21, 2.0.17, 306), 3.300 (47) (1.0.23, 2.1.15), 3.220 (16) (2.1.16, 222). The type material of

  12. Tatarinovite Ca3Al(SO4)[B(OH)4](OH)6 · 12H2O, a new ettringite-group mineral from the Bazhenovskoe deposit, Middle Urals, Russia, and its crystal structure

    NASA Astrophysics Data System (ADS)

    Chukanov, N. V.; Kasatkin, A. V.; Zubkova, N. V.; Britvin, S. N.; Pautov, L. A.; Pekov, I. V.; Varlamov, D. A.; Bychkova, Ya. V.; Loskutov, A. B.; Novgorodova, E. A.

    2016-12-01

    A new mineral, tatarinovite, ideally Ca3Al(SO4)[B(OH)4](OH)6 · 12H2O, has been found in cavities of rhodingites at the Bazhenovskoe chrysotile asbestos deposit, Middle Urals, Russia. It occurs (1) colorless, with vitreous luster, bipyramidal crystals up to 1 mm across in cavities within massive diopside, in association with xonotlite, clinochlore, pectolite and calcite, and (2) as white granular aggregates up to 5 mm in size on grossular with pectolite, diopside, calcite, and xonotlite. The Mohs hardness is 3; perfect cleavage on (100) is observed. D meas = 1.79(1), D calc = 1.777 g/cm3. Tatarinovite is optically uniaxial (+), ω = 1.475(2), ɛ = 1.496(2). The IR spectrum contains characteristic bands of SO4 2-, CO3 2-, B(OH)4 -, B(OH)3, Al(OH)6 3-, Si(OH)6 2-, OH-, and H2O. The chemical composition of tatarinovite (wt %; ICP-AES; H2O was determined by the Alimarin method; CO2 was determined by selective sorption on askarite) is as follows: 27.40 CaO, 4.06 B2O3, 6.34 A12O3, 0.03 Fe2O3, 2.43 SiO2, 8.48 SO3, 4.2 CO2, 46.1 H2O, total is 99.04. The empirical formula (calculated on the basis of 3Ca apfu) is H31.41Ca3.00(Al0.76Si0.25)Σ1.01 · (B0.72S0.65C0.59)Σ1.96O24.55. Tatarinovite is hexagonal, space gr. P63, a = 11.1110(4) Å, c = 10.6294(6) Å, V = 1136.44(9) A3, Z = 2. Its crystal chemical formula is Ca3(Al0.70Si0.30) · {[SO4]0.34[B(OH)4]0.33[CO3]0.24}{[SO4]0.30[B(OH)4]0.34[CO3]0.30[B(OH)3]0.06}(OH5·73O0.27) · 12H2O. The strongest reflections of the powder X-ray diffraction pattern [ d, Å ( I, %) ( hkl)] are 9.63 (100) (100), 5.556 (30) (110), 4.654 (14) (102), 3.841 (21) (112), 3.441 (12) (211), 2.746 (10) (302), 2.538 (12) (213). Tatarinovite was named in memory of the Russian geologist and petrologist Pavel Mikhailovich Tatarinov (1895-1976), a well-known specialist in chrysotile asbestos deposits. Type specimens have been deposited at the Fersman Mineralogical Museum of the Russian Academy of Sciences, Moscow.

  13. Lavoisierite, Mn2+ 8[Al10(Mn3+Mg)][Si11P]O44(OH)12, a new mineral from Piedmont, Italy: the link between "ardennite" and sursassite

    NASA Astrophysics Data System (ADS)

    Orlandi, Paolo; Biagioni, Cristian; Pasero, Marco; Mellini, Marcello

    2013-03-01

    The new mineral species lavoisierite, ideally Mn2+ 8[Al10(Mn3+Mg)][Si11P]O44(OH)12, has been discovered in piemontite-bearing micaschists belonging to the Piedmontese Nappe from Punta Gensane, Viù Valley, Western Alps, Italy. It occurs as yellow-orange acicular to prismatic-tabular crystals up to a few millimeters in length, with white streak and vitreous luster, elongated along [010] and flattened on {001}. Lavoisierite is associated with quartz, "mica," sursassite, piemontite, spessartine, braunite, and "tourmaline." Calculated density is 3.576 g cm-3. In plane-polarized light, it is transparent, pleochroic, with pale yellow parallel to [010] and yellow-orange normal to this direction; extinction is parallel and elongation is positive. Birefringence is moderate; the calculated average refraction index n is 1.750. Lavoisierite is orthorhombic, space group Pnmm, with a 8.6891(10), b 5.7755(3), c 36.9504(20) Å, V 1854.3(2) Å3, Z = 2. Calculated main diffraction lines of the X-ray powder diffraction pattern are [ d in Å, ( I), ( hkl); relative intensities are visually estimated]: 4.62 (m) (112), 2.931 (vs) (11 10), 2.765 (s) (11 11), 2.598 (s) (310), 2.448 (ms) (028). Chemical analyses by electron microprobe give (in wt%) P2O5 2.08, V2O5 0.37, SiO2 34.81, TiO2 0.13, Al2O3 22.92, Cr2O3 0.32, Fe2O3 0.86, Mn2O3 6.92, MnO 19.09, MgO 5.73, CaO 1.94, Na2O 0.01, H2O 5.44, sum 100.62 wt%. H2O content was calculated from structure refinement. The empirical formula, based on 56 anions, is (Mn{5.340/2+}Mg1.810Ca0.686Na0.006)Σ=7.852(Al8.921Mn{1.739/3+}Mg1.010Fe{0.214/3+}Cr0.084Ti0.032)Σ=12.000(Si11.496P0.582V0.081)Σ=12.159O43.995(OH)12.005. The crystal structure of lavoisierite was solved by direct methods and refined on the basis of 1743 observed reflections to R 1 = 4.6 %. The structure is characterized by columns of edge-sharing octahedra running along [010] and linked to each other by means of [SiO4], [Si2O7], and [Si3O10] groups. Lavoisierite, named after the French

  14. Rocks and Minerals.

    ERIC Educational Resources Information Center

    Naturescope, 1987

    1987-01-01

    Provides background information on rocks and minerals, including the unique characteristics of each. Teaching activities on rock-hunting and identification, mineral configurations, mystery minerals, and growing crystals are provided. Reproducible worksheets are included for two of the activities. (TW)

  15. Mineral spirits poisoning

    MedlinePlus

    Mineral spirits are liquid chemicals used to thin paint and as a degreaser. Mineral spirits poisoning occurs ... be found in: Mineral spirits ( Stoddard solvent ) Some paints Some floor and furniture waxes and polishes Some ...

  16. Vitamins and Minerals

    MedlinePlus

    ... and Minerals? What Do Vitamins and Minerals Do? Fuel for Growth Common Concerns en español Vitaminas y minerales Breakfast cereals advertise that they're packed with vitamins and minerals. Sports drinks claim they can rev up your flagging energy with a jolt of vitamins or minerals (sorry, ...

  17. Minerals in our environment

    USGS Publications Warehouse

    Weathers, Judy; Galloway, John; Frank, Dave

    2000-01-01

    Minerals are found everywhere in our daily lives. This poster depicts numerous items found throughout a home, and the mineral(s) or mineral resources used in the ingredients of, or construction/manufacturing of those items. Designed for K-8 Teachers this poster can be scaled and is printable at 36" x 60" and legible at 11" x 17" in size.

  18. Diagnosing ALS

    MedlinePlus

    ... that a person diagnosed with ALS seek a second opinion from an ALS "expert" - someone who diagnoses and treats many ALS patients and has training in this medical specialty. The ALS Association maintains a list of recognized experts in the field of ALS. See ALS Association Certified Centers of ...

  19. A Developed Spectral Identification Tree for Mineral Mapping using Hyperspectral Data

    NASA Astrophysics Data System (ADS)

    Gan, Fuping; Wang, Runsheng; Yan, Bokun; Shang, Kun

    2016-04-01

    The relationship between the spectral features and the composition of minerals are the basis of mineral identification using hyperspectral data. The reflectance spectrum of minerals results from the systematic combination of several modes of interaction between electromagnetic energy and mineral particles in the form of reflection and absorption. Minerals tend to have absorbing features at specific wavelengths with a characteristic shape, which can be used as diagnostic indicators for identification. The spectral identification tree (SIT) method for mineral identification is developed in our research to map minerals accurately and applied in some typical mineral deposits in China. The SIT method is based on the diagnostic absorption features of minerals through comparing and statistically analyzing characteristic spectral data of minerals. We establish several levels of identification rules for the type, group and species of minerals using IF-THEN rule according to the spectral identification criteria so that the developed SIT can be further used to map minerals at different levels of detail from mineral type to mineral species. Identifiable minerals can be grouped into six types: Fe2+-bearing, Fe3+-bearing, Mn2+-bearing, Al-OH-bearing, Mg-OH-bearing and carbonate minerals. Each type can be further divided into several mineral groups. Each group contains several mineral species or specific minerals. A mineral spectral series, therefore, can be constructed as "type-group-species-specific mineral (mineral variety)" for mineral spectral identification. It is noted that the mineral classification is based mainly on spectral reflectance characteristics of minerals which may not be consistent with the classification in mineralogy. We applied the developed SIT method to the datasets acquired at the Eastern Tianshan Mountains of Xinjiang (HyMap data) and the Qulong district of Xizang (Hyperion data). In Xinjiang, the two major classes of Al-OH and Mg-OH minerals were

  20. Computer simulation studies of minerals

    NASA Astrophysics Data System (ADS)

    Oganov, Artem Romaevich

    Applications of state-of-the-art computer simulations to important Earth- and rock-forming minerals (Al2SiO5 polymorphs, albite (NaAlSi3O8), and MgSiO3 perovskite) are described. Detailed introductions to equations of state and elasticity, phase transitions, computer simulations, and geophysical background are given. A new general classification of phase transitions is proposed, providing a natural framework for discussion of structural, thermodynamic, and kinetic aspects of phase transitions. The concept of critical bond distances is introduced. For Si-O bonds this critical distance is 2.25 A. Using atomistic simulations, anomalous Al-Si antiordering in albite is explained. A first-order isosymmetric transition associated with a change in the ordering scheme is predicted at high pressures. A quantum-mechanical study is presented for the Al2SiO5 polymorphs: kyanite, andalusite, sillimanite, and hypothetical pseudobrookite-like and V3O5-like phases (the latter phase was believed to be the main Al mineral of the lower mantle). It is shown that above 11 GPa all the Al2SiO5 phases break down into the mixture of oxides: corundum (Al2O3) and stishovite (SiO2). Atomisation energies, crystal structures and equations of state of all the Al2SiO5 polymorphs, corundum, stishovite, quartz (SiO2) have been determined. Metastable pressure-induced transitions in sillimanite and andalusite are predicted at ~30-50 GPa and analysed in terms of structural changes and lattice dynamics. Sillimanite (Pbnm) transforms into incommensurate and isosymmetric (Pbnm) phases; andalusite undergoes pressure-induced amorphisation. Accurate quantum-mechanical thermal equation of state is obtained for MgSiO3 perovskite, the main Earth-forming mineral. Results imply that a pure-perovskite mantle is unlikely. I show that MgSiO3 perovskite is not a Debye-like solid, contrary to a common assumption. First ever ab initio molecular dynamics calculations of elastic constants at finite temperatures are

  1. Crystal structure of the mineral (Na,Ca,K){sub 2}(Ca,Na){sub 4}(Mg,Fe){sub 5}(Mg,Fe,Ti){sub 5}[Si{sub 12}Al{sub 4}O{sub 44}](F,O){sub 4}: a triclinic representative of the amphibole family

    SciTech Connect

    Rastsvetaeva, R. K. Aksenov, S. M.

    2012-05-15

    A mineral belonging to the amphibole family found at the Rothenberg paleovolcano (Eifel, Germany) was studied by single-crystal X-ray diffraction. The triclinic pseudomonoclinic unit-cell parameters are a = 5.3113(1) Angstrom-Sign , b = 18.0457(3) Angstrom-Sign ; c = 9.8684(2) Angstrom-Sign , {alpha} = 90.016(2) Degree-Sign , {beta} = 105.543(4) Degree-Sign , {gamma} = 89.985(2) Degree-Sign . The structure was solved by direct methods in sp. gr. P1 and refined to the R factor of 2.7% based on 6432 reflections with |F| > 3{sigma}(F) taking into account twinning. The mineral with the idealized formula (Na,Ca,K){sub 2}(Ca,Na){sub 4}(Mg,Fe){sub 5}(Mg,Fe,Ti){sub 5}[Si{sub 12}Al{sub 4}O{sub 44}](F,O){sub 4} has some symmetry and structural features that distinguish it from other minerals of this family.

  2. Some problems of bacterial mineralization and sedimentation

    NASA Astrophysics Data System (ADS)

    Rozanov, Alexei Y.

    2003-01-01

    Owing to the latest investigations in bacterial paleontology and geomicrobiology a number of minerals known to be formed with the participation of micro-organisms increases continuously. 12 - 15 years ago we know nearly 20 minerals: carbonates (calcite, aragonite, monohydrocalcite), phosphates (dalite, francolite, struvite, vivianite, and some other), sulfates (jarosite), ferric oxides (magnetite, ferrohydrite), sulfides (pyrite, hydrotroilite, sphalerite, wurtzite, and some others) (Lowernstan, Weiner, 1989). Now their number is several times greater. Quartz cristobalite, pyrolusite, silicates (including layer ones), and feldspars are of special interest (Geomicrobiology..., 1997; Tazaki et al., 1997; Geptner et al., 1997; Bacterial paleontology, 2002).

  3. Aluminum Trichloride Inhibits the Rat Osteoblasts Mineralization In Vitro.

    PubMed

    Song, Miao; Huo, Hui; Cao, Zheng; Han, Yanfei; Gao, Li

    2017-01-01

    Aluminum (Al) is an accumulative toxic metal. Excessive Al accumulation inhibits osteoblasts mineralization and induces osteoporosis. However, the inhibition mechanism of Al on the mineralization is not fully understood. Thus, in this study, the rat osteoblasts were cultured and exposed to 0 mmol L(-1) (control group, CG) and 0.52 mmol L(-1) aluminum trichloride (AlCl3, treatment group, TG) for 7, 14, and 21 days, respectively. We found that mineralized matrix nodules, the activity of bone alkaline phosphatase, the concentration of extracellular calcium, the mRNA expression of type-I collagen, the mRNA and protein expressions of osteopontin, osteocalcin, and bone sialoprotein were all decreased, while the concentration of extracellular phosphorus was increased in TG compared with CG with time prolonged. Taken together, these results indicated that AlCl3 inhibited osteoblasts mineralization in vitro.

  4. Bartering for Minerals.

    ERIC Educational Resources Information Center

    May, Kathie

    2002-01-01

    Presents an activity in which students are assigned occupations that rely on specific minerals. To obtain the needed minerals, students learn how to trade services and commodities. Includes details on preparation, modeling behaviors, and printed materials. (DDR)

  5. Mineral Spirits Purification Process.

    DTIC Science & Technology

    the mineral spirits to decompose 1,2- propanediol dinitrate and remove hydrogen cyandide and other gaseous decomposition produces, and then distill the mineral spirits from the remaining contaminants.

  6. Possible uranium mineralization, Mineral Mountains, Utah

    USGS Publications Warehouse

    Miller, W. Roger; McHugh, John B.; Ficklin, Walter H.

    1979-01-01

    The Mineral Mountains block in west-central Utah is a horst whose core stands structurally high relative to all nearby basin-and-range fault blocks. Rocks of the Mineral Mountains range from Precambrian to Quaternary in age, but mostly consist of Tertiary granitic rocks. The range lies with the Wah Wah-Tusher mineral belt. Lead, silver, gold, and tungsten have been mined commercially. During a geochemical survey conducted in the summer of 1978, 30 water samples and 29 stream-sediment samples were collected from the Mineral Mountains area. The interpretation of simple plots of uranium concentrations and the results of a Q-mode factor analysis indicate that potential exists for uranium mineral deposits within the Mineral Mountains. The most favorable areas are in the granitic pluton near its contacts with sedimentary and metamorphic rocks. The most likely source of the uranium anomalies is uraninite-bearing epigenic veins along faults and fractures within the pluton. Three hypothetical models are proposed to account for the uranium mineralization.

  7. Minerals leasing for landowners

    SciTech Connect

    Not Available

    1983-01-01

    This report delineates the provisions of the legal codes of the 13 Southeastern states relating to minerals leasing. The introduction explains land ownership and land leasing in terms of mineral rights, and describes the basic elements which a lease conveyance must contain to be valid. A checklist gives the terms which must be included in all mineral leases.

  8. ALS Association

    MedlinePlus

    ... toward a world without ALS! Walk to Defeat ALS® Walk to Defeat ALS® draws people of all ... We need your help. I Will Advocate National ALS Registry The National ALS Registry is a congressionally ...

  9. Moon's Pink Mineral

    NASA Astrophysics Data System (ADS)

    Martel, L. M. V.; Taylor, G. J.

    2014-12-01

    Since the 2010 remote-sensing discovery of lunar regolith rich in Mg-Al spinel on the rims and central peaks of impact craters and inner rings of basins on the Moon, researchers have been designing experiments to better understand the origin and formation history of spinel-rich rocks and what they mean for the construction of the lunar crust. The newly detected rock type is referred to as pink spinel anorthosite, or PSA, due to high plagioclase and low abundance (<5%) of mafic minerals such as olivine and pyroxene. Two recent studies tested specific hypotheses of PSA production on the Moon. Juliane Gross (American Museum of Natural History and the Lunar and Planetary Institute, LPI) and colleagues at the LPI, University of Hawaii, and NASA Johnson Space Center conducted experiments to model the crystallization of spinel in impact melts from impact events. Tabb Prissel (Brown University) and colleagues from Brown conducted experiments to model a plutonic formation of spinel from magma-wallrock interactions. In each study, comparisons of the remote sensing data with Apollo lunar samples or lunar meteorites were crucial for testing the PSA formation hypotheses with the experimental results. Definitive answers aren't in yet. PSA could form from impact melting of the right target rocks. Equally likely is PSA formation by reaction of basaltic magma and crust. One big unknown is the effect space weathering has in determining the amount of spinel in the PSA..

  10. Mineral particles, mineral fibers, and lung cancer

    SciTech Connect

    Churg, A.; Wiggs, B.

    1985-08-01

    The total fibrous and nonfibrous mineral content of the lung has been analyzed in a series of 14 men with lung cancer but no history of occupational dust exposure, and in a series of 14 control men matched for age, smoking history, and general occupational class. The lung cancer patients had an average of 525 +/- 369 X 10(6) exogenous mineral particles and 17.4 +/- 19.6 X 10(6) exogenous mineral fibers/g dry lung, while the controls had averages of 261 +/- 175 mineral particles and 4.7 +/- 3.2 X 10(6) mineral fibers/g dry lung. These differences are statistically significant for both particles and fibers. Kaolinite, talc, mica, feldspars, and crystalline silica comprised the majority of particles of both groups. Approximately 90% of the particles were smaller than 2 micron in diameter and approximately 60% smaller than 1 micron. In both groups, patients who had smoked more than 35 pack years had greater numbers of particles than patients who had smoked less than 35 pack years. It is concluded that, in this study, lungs from patients with lung cancer had statistically greater numbers of mineral particles and fibers than lungs from controls, and that smoking influences total long-term retention of particles from all sources.

  11. Distinct Mineral Weathering Behaviors of the Novel Mineral-Weathering Strains Rhizobium yantingense H66 and Rhizobium etli CFN42

    PubMed Central

    Chen, Wei; Luo, Long; He, Lin-Yan; Wang, Qi

    2016-01-01

    ABSTRACT Bacteria play important roles in mineral weathering, soil formation, and element cycling. However, little is known about the interaction between silicate minerals and rhizobia. In this study, Rhizobium yantingense H66 (a novel mineral-weathering rhizobium) and Rhizobium etli CFN42 were compared with respect to potash feldspar weathering, mineral surface adsorption, and metabolic activity during the mineral weathering process. Strain H66 showed significantly higher Si, Al, and K mobilization from the mineral and higher ratios of cell numbers on the mineral surface to total cell numbers than strain CFN42. Although the two strains produced gluconic acid, strain H66 also produced acetic, malic, and succinic acids during mineral weathering in low- and high-glucose media. Notably, higher Si, Al, and K releases, higher ratios of cell numbers on the mineral surface to total cell numbers, and a higher production of organic acids by strain H66 were observed in the low-glucose medium than in the high-glucose medium. Scanning electron microscope analyses of the mineral surfaces and redundancy analysis showed stronger positive correlations between the mineral surface cell adsorption and mineral weathering, indicated by the dissolved Al and K concentrations. The results showed that the two rhizobia behaved differently with respect to mineral weathering. The results suggested that Rhizobium yantingense H66 promoted potash feldspar weathering through increased adsorption of cells to the mineral surface and through differences in glucose metabolism at low and high nutrient concentrations, especially at low nutrient concentrations. IMPORTANCE This study reported the potash feldspar weathering, the cell adsorption capacity of the mineral surfaces, and the metabolic differences between the novel mineral-weathering Rhizobium yantingense H66 and Rhizobium etli CFN42 under different nutritional conditions. The results showed that Rhizobium yantingense H66 had a greater ability

  12. Magnetic susceptibilities of minerals

    USGS Publications Warehouse

    Rosenblum, Sam; Brownfield, I.K.

    2000-01-01

    Magnetic separation of minerals is a topic that is seldom reported in the literature for two reasons. First, separation data generally are byproducts of other projects; and second, this study requires a large amount of patience and is unusually tedious. Indeed, we suspect that most minerals probably are never investigated for this property. These data are timesaving for mineralogists who concentrate mono-mineralic fractions for chemical analysis, age dating, and for other purposes. The data can certainly be used in the ore-beneficiation industries. In some instances, magnetic-susceptibility data may help in mineral identification, where other information is insufficient. In past studies of magnetic separation of minerals, (Gaudin and Spedden, 1943; Tille and Kirkpatrick, 1956; Rosenblum, 1958; Rubinstein and others, 1958; Flinter, 1959; Hess, 1959; Baker, 1962; Meric and Peyre, 1963; Rojas and others, 1965; and Duchesne, 1966), the emphasis has been on the ferromagnetic and paramagnetic ranges of extraction. For readers interested in the history of magnetic separation of minerals, Krumbein and Pettijohn (1938, p. 344-346) indicated nine references back to 1848. The primary purpose of this paper is to report the magnetic-susceptibility data on as many minerals as possible, similar to tables of hardness, specific gravity, refractive indices, and other basic physical properties of minerals. A secondary purpose is to demonstrate that the total and best extraction ranges are influenced by the chemistry of the minerals. The following notes are offered to help avoid problems in separating a desired mineral concentrate from mixtures of mineral grains.

  13. 43 CFR 19.8 - Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest...

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 1 2014-10-01 2014-10-01 false Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest Wilderness. 19.8 Section 19.8 Public Lands: Interior... § 19.8 Prospecting, mineral locations, mineral patents, and mineral leasing within National...

  14. 43 CFR 19.8 - Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest...

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 1 2012-10-01 2011-10-01 true Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest Wilderness. 19.8 Section 19.8 Public Lands: Interior... § 19.8 Prospecting, mineral locations, mineral patents, and mineral leasing within National...

  15. 43 CFR 19.8 - Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest...

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest Wilderness. 19.8 Section 19.8 Public Lands: Interior... § 19.8 Prospecting, mineral locations, mineral patents, and mineral leasing within National...

  16. 43 CFR 19.8 - Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest...

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 1 2013-10-01 2013-10-01 false Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest Wilderness. 19.8 Section 19.8 Public Lands: Interior... § 19.8 Prospecting, mineral locations, mineral patents, and mineral leasing within National...

  17. 43 CFR 19.8 - Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest...

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 1 2011-10-01 2011-10-01 false Prospecting, mineral locations, mineral patents, and mineral leasing within National Forest Wilderness. 19.8 Section 19.8 Public Lands: Interior... § 19.8 Prospecting, mineral locations, mineral patents, and mineral leasing within National...

  18. Reagan issues mineral policy

    NASA Astrophysics Data System (ADS)

    The National Materials and Minerals Program plan and report that President Reagan sent to Congress on April 5 aims to ‘decrease America's minerals vulnerability’ while reducing future dependence on potentially unstable foreign sources of minerals. These goals would be accomplished by taking inventory of federal lands to determine mineral potential; by meeting the stockpile goals set by the Strategic and Critical Material Stockpiling Act; and by establishing a business and political climate that would encourage private-sector research and development on minerals.Now that the Administration has issued its plan, the Subcommittee on Mines and Mining of the House Committee on Interior and Insular Affairs will consider the National Minerals Security Act (NMSA), which was introduced 1 year ago by subcommittee chairman Jim Santini (D-Nev.) [Eos, May 19, 1981, p. 497]. The bill calls for establishing a three-member White-House-level council to coordinate the development of a national minerals policy; amending tax laws to assist the mining industry to make capital investments to locate and produce strategic materials; and creating a revolving fund for the sale and purchase of strategic minerals. In addition, the NMSA bill would allow the secretary of the interior to make previously withdrawn public lands available for mineral development. The subcommittee will hold a hearing on the Administration's plan on May 11. Interior Secretary James Watt has been invited to testify.

  19. Mineral Processing Sector

    EPA Pesticide Factsheets

    Find environmental regulatory and compliance information for the nonmetallic mineral processing sector (NAICS 327), including NESHAPs for asbestos and hazardous waste, and wastewater permit information.

  20. Elemental composition of biomineralized amorphous mineral granules isolated from ants: correlation with ingested mineral particles from the soil.

    PubMed

    Carneiro, Fabricia G; Keim, Carolina N; Acosta-Avalos, Daniel; Farina, Marcos

    2013-01-01

    Amorphous mineral granules are formed by concentric mineral layers containing polyphosphate, pyrophosphate and/or orthophosphate and several metallic cations such as Mg(2+), Ca(2+), K(+), Mn(2+), Fe(3+), Cu(2+), and Zn(2+). In this work, we analyzed amorphous mineral granules isolated from the ant species Camponotus abdominalis, Camponotus sp., Acromyrmex subterraneus and Pachycondyla marginata by energy-dispersive X-ray analysis. The elemental composition of the granules was compared to that of mineral particles, probably soil particles, to access the influence of the environment and of specific characteristics of each ant species in the elemental composition of the amorphous mineral granules. Both the granules and mineral particles presented Mg, Ca, Fe, and Zn in the four species. Additionally, Al tended to be present in both (or none) of the two types of material in a given ant species, suggesting that the aluminum found in the amorphous mineral granules could be derived from ingested soil particles. On the other hand, Sr was found in the amorphous mineral granules of some of the studied ant species, but not in the mineral particles. The fact that 3/4 of the elements found in the granules were found also in the mineral particles suggests that the mineral composition of the soil plays a fundamental role in the accumulation of some elements in the amorphous mineral granules of ants. These results suggest a major role of soil particles as a source of micronutrients for the four ant species.

  1. ALS - resources

    MedlinePlus

    Resources - ALS ... The following organizations are good resources for information on amyotrophic lateral sclerosis : Muscular Dystrophy Association -- www.mda.org/disease/amyotrophic-lateral-sclerosis National Amyotrophic Lateral Sclerosis (ALS) ...

  2. 36 CFR 293.14 - Mineral leases and mineral permits.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 36 Parks, Forests, and Public Property 2 2010-07-01 2010-07-01 false Mineral leases and mineral... AGRICULTURE WILDERNESS-PRIMITIVE AREAS § 293.14 Mineral leases and mineral permits. (a) All laws pertaining to mineral leasing shall extend to each National Forest Wilderness for the period specified in the...

  3. 36 CFR 293.14 - Mineral leases and mineral permits.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 36 Parks, Forests, and Public Property 2 2011-07-01 2011-07-01 false Mineral leases and mineral... AGRICULTURE WILDERNESS-PRIMITIVE AREAS § 293.14 Mineral leases and mineral permits. (a) All laws pertaining to mineral leasing shall extend to each National Forest Wilderness for the period specified in the...

  4. 36 CFR 293.14 - Mineral leases and mineral permits.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 36 Parks, Forests, and Public Property 2 2012-07-01 2012-07-01 false Mineral leases and mineral... AGRICULTURE WILDERNESS-PRIMITIVE AREAS § 293.14 Mineral leases and mineral permits. (a) All laws pertaining to mineral leasing shall extend to each National Forest Wilderness for the period specified in the...

  5. 36 CFR 293.14 - Mineral leases and mineral permits.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 36 Parks, Forests, and Public Property 2 2014-07-01 2014-07-01 false Mineral leases and mineral... AGRICULTURE WILDERNESS-PRIMITIVE AREAS § 293.14 Mineral leases and mineral permits. (a) All laws pertaining to mineral leasing shall extend to each National Forest Wilderness for the period specified in the...

  6. 36 CFR 293.14 - Mineral leases and mineral permits.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 36 Parks, Forests, and Public Property 2 2013-07-01 2013-07-01 false Mineral leases and mineral... AGRICULTURE WILDERNESS-PRIMITIVE AREAS § 293.14 Mineral leases and mineral permits. (a) All laws pertaining to mineral leasing shall extend to each National Forest Wilderness for the period specified in the...

  7. Mineral Fiber Toxicology

    EPA Science Inventory

    The chemical and physical properties of different forms of mineral fibers impact biopersistence and pathology in the lung. Fiber chemistry, length, aspect ratio, surface area and dose are critical factors determining mineral fiber-associated health effects including cancer and as...

  8. Digging into Minnesota Minerals.

    ERIC Educational Resources Information Center

    Minnesota State Dept. of Natural Resources, St. Paul.

    This publication presents students with facts about geology and several learning activities. Topics covered include rocks and minerals, volcanoes and earthquakes, fossils, exploration geology, mining in Minnesota, environmental issues related to mining, mineral uses, mining history, and the geology of Minnesota's state parks. A geologic timetable…

  9. Mineral physics abroad

    NASA Astrophysics Data System (ADS)

    Liebermann, Robert

    During the 1983-1984 academic year, I spent a sabbatical leave in France, during which I had the opportunity to visit several mineral physics laboratories in Europe and meet many of our colleagues there. The purpose of this item is to report briefly on developments of interest to the U.S. mineral physics community.

  10. Mineral commodity summaries 2016

    USGS Publications Warehouse

    Ober, Joyce A.

    2016-01-01

    This report is the earliest Government publication to furnish estimates covering 2015 nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for more than 90 individual minerals and materials

  11. Vitamins, Minerals, and Mood

    ERIC Educational Resources Information Center

    Kaplan, Bonnie J.; Crawford, Susan G.; Field, Catherine J.; Simpson, J. Steven A.

    2007-01-01

    In this article, the authors explore the breadth and depth of published research linking dietary vitamins and minerals (micronutrients) to mood. Since the 1920s, there have been many studies on individual vitamins (especially B vitamins and Vitamins C, D, and E), minerals (calcium, chromium, iron, magnesium, zinc, and selenium), and vitamin-like…

  12. Mineral Wool Insulation Binders

    NASA Astrophysics Data System (ADS)

    Kowatsch, Stefan

    Mineral wool is considered the best known insulation type among the wide variety of insulation materials. There are three types of mineral wool, and these consist of glass, stone (rock), and slag wool. The overall manufacturing processes, along with features such as specifications and characteristics for each of these types, as well as the role of the binder within the process are described.

  13. Mineral Commodity Summaries 2002

    USGS Publications Warehouse

    ,

    2002-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  14. Mineral Commodity Summaries 2005

    USGS Publications Warehouse

    ,

    2005-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  15. Mineral Commodity Summaries 2001

    USGS Publications Warehouse

    ,

    2001-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  16. Mineral Commodity Summaries 2007

    USGS Publications Warehouse

    ,

    2007-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  17. Mineral Commodity Summaries 2006

    USGS Publications Warehouse

    ,

    2006-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  18. Mineral Commodity Summaries 1998

    USGS Publications Warehouse

    ,

    1998-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  19. Mineral Commodity Summaries 1997

    USGS Publications Warehouse

    ,

    1997-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials

  20. Mineral Commodity Summaries 1999

    USGS Publications Warehouse

    ,

    1999-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  1. Mineral Commodity Summaries 2003

    USGS Publications Warehouse

    ,

    2003-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  2. Mineral Commodity Summaries 2004

    USGS Publications Warehouse

    ,

    2004-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  3. Mineral Commodity Summaries 2000

    USGS Publications Warehouse

    ,

    2000-01-01

    Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.

  4. Mineral commodity summaries 2017

    USGS Publications Warehouse

    Ober, Joyce A.

    2017-01-31

    This report is the earliest Government publication to furnish estimates covering 2016 nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for more than 90 individual minerals and materials.

  5. Mineral Commodity Summaries 2011

    USGS Publications Warehouse

    ,

    2011-01-01

    Each chapter of the 2011 edition of the U.S. Geological Survey (USGS) Mineral Commodity Summaries (MCS) includes information on events, trends, and issues for each mineral commodity as well as discussions and tabular presentations on domestic industry structure, Government programs, tariffs, 5-year salient statistics, and world production and resources. The MCS is the earliest comprehensive source of 2010 mineral production data for the world. More than 90 individual minerals and materials are covered by two-page synopses. For mineral commodities for which there is a Government stockpile, detailed information concerning the stockpile status is included in the two-page synopsis. Mineral Commodity Summaries 2011 contains new chapters on iron oxide pigments, wollastonite, and zeolites. The chapters on mica (natural), scrap and flake and mica (natural), sheet have been combined into a single chapter - mica (natural). Abbreviations and units of measure, and definitions of selected terms used in the report, are in Appendix A and Appendix B, respectively. "Appendix C - Reserves and Resources" has been divided into "Part A - Resource/Reserve Classification for Minerals" and "Part B - Sources of Reserves Data," including some information that was previously in this introduction. A directory of USGS minerals information country specialists and their responsibilities is Appendix D. The USGS continually strives to improve the value of its publications to users. Constructive comments and suggestions by readers of the MCS 2011 are welcomed.

  6. Underground mineral extraction

    NASA Technical Reports Server (NTRS)

    Miller, C. G.; Stephens, J. B.

    1980-01-01

    A method was developed for extracting underground minerals such as coal, which avoids the need for sending personnel underground and which enables the mining of steeply pitched seams of the mineral. The method includes the use of a narrow vehicle which moves underground along the mineral seam and which is connected by pipes or hoses to water pumps at the surface of the Earth. The vehicle hydraulically drills pilot holes during its entrances into the seam, and then directs sideward jets at the seam during its withdrawal from each pilot hole to comminute the mineral surrounding the pilot hole and combine it with water into a slurry, so that the slurried mineral can flow to a location where a pump raises the slurry to the surface.

  7. Mechanism of aluminium bio-mineralization in the apoferritin cavity

    NASA Astrophysics Data System (ADS)

    Chiarpotto, M.; Ciasca, G.; Vassalli, M.; Rossi, C.; Campi, G.; Ricci, A.; Bocca, B.; Pino, A.; Alimonti, A.; De Sole, P.; Papi, M.

    2013-08-01

    Many experimental evidences point out the correlation between the presence of aluminum-ferritin complex and neursopathological disorders. In these complexes, two different ranges of Aluminium (Al) atoms are usually found, i.e., just few atoms or several hundreds. Here, we investigated the in-vitro Al-apoferritin binding, with the aim to elucidate the mechanism behind the formation of Al-ferritin complexes in-vivo. To this purpose, we studied the mineralization of Al in its ionic and complexed form with citrate demonstrating that high Al levels found in clinical studies can be obtained only conveying Al by small physiological ligands.

  8. {sup 13}C chemical shift anisotropies for carbonate ions in cement minerals and the use of {sup 13}C, {sup 27}Al and {sup 29}Si MAS NMR in studies of Portland cement including limestone additions

    SciTech Connect

    Sevelsted, Tine F.; Herfort, Duncan

    2013-10-15

    {sup 13}C isotropic chemical shifts and chemical shift anisotropy parameters have been determined for a number of inorganic carbonates relevant in cement chemistry from slow-speed {sup 13}C MAS or {sup 13}C({sup 1}H) CP/MAS NMR spectra (9.4 T or 14.1 T) for {sup 13}C in natural abundance. The variation in the {sup 13}C chemical shift parameters is relatively small, raising some doubts that different carbonate species in Portland cement-based materials may not be sufficiently resolved in {sup 13}C MAS NMR spectra. However, it is shown that by combining {sup 13}C MAS and {sup 13}C({sup 1}H) CP/MAS NMR carbonate anions in anhydrous and hydrated phases can be distinguished, thereby providing valuable information about the reactivity of limestone in cement blends. This is illustrated for three cement pastes prepared from an ordinary Portland cement, including 0, 16, and 25 wt.% limestone, and following the hydration for up to one year. For these blends {sup 29}Si MAS NMR reveals that the limestone filler accelerates the hydration for alite and also results in a smaller fraction of tetrahedrally coordinated Al incorporated in the C-S-H phase. The latter result is more clearly observed in {sup 27}Al MAS NMR spectra of the cement–limestone blends and suggests that dissolved aluminate species in the cement–limestone blends readily react with carbonate ions from the limestone filler, forming calcium monocarboaluminate hydrate. -- Highlights: •{sup 13}C chemical shift anisotropies for inorganic carbonates from {sup 13}C MAS NMR. •Narrow {sup 13}C NMR chemical shift range (163–171 ppm) for inorganic carbonates. •Anhydrous and hydrated carbonate species by {sup 13}C MAS and {sup 13}C({sup 1}H) CP/MAS NMR. •Limestone accelerates the hydration for alite in Portland – limestone cements. •Limestone reduces the amount of aluminium incorporated in the C-S-H phase.

  9. Minerals yearbook, 1993. Volume 1. Metals and minerals. Annual report

    SciTech Connect

    1993-12-31

    This edition of the Mineral Yearbook discusses the performance of the worlwide minerals and materials industry during 1993 and provides background information to assist in interpreting that performance. Volume 1, Metals and Minerals, contains chapters on virtually all metallic and industrial mineral commodities important to the U.S. economy. A chapter on survey methods with a statistical summary of nonfuel minerals, and a chapters on trends in mining and quarrying in the metals and industrial mineral industries are also included.

  10. Minerals Yearbook, centennial edition 1981. Volume I. Metals and minerals

    SciTech Connect

    Not Available

    1983-01-01

    This edition of the Minerals Yearbook Marks the centennial of the first annual publication of comprehensive mineral industry statistics by the Federal Government. This volume of the Minerals Yearbook, covering metals and minerals, contains 71 commodity or commodity group chapters with data on approximately 90 minerals that were obtained as a result of the mineral information gathering activities of the Bureau of Mines. In addition, the volume contains a chapter on mining and quarrying trends and a statistical summary.

  11. Elastic properties of minerals

    SciTech Connect

    Aleksandrov, K.S.; Prodaivoda, G.T.

    1993-09-01

    Investigations of the elastic properties of the main rock-forming minerals were begun by T.V. Ryzhova and K.S. Aleksandrov over 30 years ago on the initiative of B.P. Belikov. At the time, information on the elasticity of single crystals in general, and especially of minerals, was very scanty. In the surveys of that time there was information on the elasticity of 20 or 30 minerals. These, as a rule, did not include the main rock-forming minerals; silicates were represented only by garnets, quartz, topaz, tourmaline, zircon, beryl, and staurolite, which are often found in nature in the form of large and fairly high-quality crystals. Then and even much later it was still necessary to prove a supposition which now seems obvious: The elastic properties of rocks, and hence the velocities of elastic (seismic) waves in the earth`s crust, are primarily determined by the elastic characteristics of the minerals composing these rocks. Proof of this assertion, with rare exceptions of mono-mineralic rocks (marble, quartzite, etc.) cannot be obtained without information on the elasticities of a sufficiently large number of minerals, primarily framework, layer, and chain silicates which constitute the basis of most rocks. This also served as the starting point and main problem of the undertakings of Aleksandrov, Ryzhova, and Belikov - systematic investigations of the elastic properties of minerals and then of various rocks. 108 refs., 7 tabs.

  12. Mineral facilities of Europe

    USGS Publications Warehouse

    Almanzar, Francisco; Baker, Michael S.; Elias, Nurudeen; Guzman, Eric

    2010-01-01

    This map displays over 1,700 records of mineral facilities within the countries of Europe and western Eurasia. Each record represents one commodity and one facility type at a single geographic location. Facility types include mines, oil and gas fields, and plants, such as refineries, smelters, and mills. Common commodities of interest include aluminum, cement, coal, copper, gold, iron and steel, lead, nickel, petroleum, salt, silver, and zinc. Records include attributes, such as commodity, country, location, company name, facility type and capacity (if applicable), and latitude and longitude geographical coordinates (in both degrees-minutes-seconds and decimal degrees). The data shown on this map and in table 1 were compiled from multiple sources, including (1) the most recently available data from the U.S. Geological Survey (USGS) Minerals Yearbook (Europe and Central Eurasia volume), (2) mineral statistics and information from the USGS Minerals Information Web site (http://minerals.usgs.gov/minerals/pubs/country/europe.html), and (3) data collected by the USGS minerals information country specialists from sources, such as statistical publications of individual countries, annual reports and press releases of operating companies, and trade journals. Data reflect the most recently published table of industry structure for each country at the time of this publication. Additional information is available from the country specialists listed in table 2.

  13. A review of mineral resources in Malawi: With special reference to aluminium variation in mineral deposits

    NASA Astrophysics Data System (ADS)

    Dill, H. G.

    2007-03-01

    The lithology of Malawi is characterized by Precambrian metamorphic and igneous rocks which form part of the polyphase East African Orogen. Rift-related sedimentation and igneous activity during the late Paleozoic (Karoo System) and the late Mesozoic (Chilwa Province) have produced a great variety of rocks that underwent strong chemical weathering and erosion when the entire region received its final shape by peneplanation and fluvial incision during the Cenozoic under (sub)tropical climatic conditions. Aluminum is a dominating element in minerals (e.g., corundum, kyanite, beryl, gibbsite) in this region. Some minerals were concentrated in deposits bound to Al-enriched host rocks (zircon, pyrochlore, eudialyte, uranium minerals) with high A/CNK ratios, whereas others, e.g., asbestos, chalcedony, monazite, kaolinite, ilmenite and garnet have host rocks of a low A/CNK ratio. Aluminum was used to categorize these various mineral deposits. The abundance of aluminum and accumulations of Nb, Zr, Ti, REE, Sr and Ba point for some mineralisations to similar subcrustal carbonatite-forming systems that were operative during periods of the Precambrian and the Mesozoic in Malawi. Aluminum variation does not only reflect differentiation in the various igneous rock series but it is also visible in the sedimentary realm during transport and weathering. In context with other elements such as Ti and P, Al provides an opportunity to reveal chemical relationships between rocks and mineral deposits. Spinel and Al-enriched silicate minerals can be used as pathfinder minerals in the stream sediments to guide the exploration geologist to non-metallic deposits.

  14. Minerals Management Service: Strategic plan

    SciTech Connect

    1997-09-30

    This plan addresses the management of the mineral resources on the Outer Continental Shelf in an environmentally sound and safe manner and the timely collection, verification, and distribution of mineral revenues from Federal and Indian lands. The Minerals Management Service (MMS) manages the Nation`s natural gas, oil and other mineral resources on the Outer Continental Shelf (OCS), and collects, accounts for, and disburses revenues from offshore federal mineral leases and from onshore mineral leases on Federal and Indian lands.

  15. Australian Mineral Foundation.

    ERIC Educational Resources Information Center

    Crowe, D. S.

    1980-01-01

    Provides details on the philosophy and operation of the Australian Mineral Foundation, established in 1970 to update professionals in the mining and petroleum industries. Services in continuing education courses and to secondary school teachers and students are described. (CS)

  16. Biological effects of minerals

    SciTech Connect

    Guthrie, G.D. Jr.

    1991-09-01

    In general, clay materials exhibit a range of biological activities, from apparently inactive or slightly active, such as hematite, to highly fibrogenic and carcinogenic, such as fibrous brucite (nemalite). The zeolites also exhibit such as range, with some mordenite being slightly active and erionite being highly active; however, erionite is the only zeolite that has been studied extensively. The diversity of mineral species holds great potential for probing these mechanisms, especially when mineralogical data are integrated with biological data. Unfortunately, many of the studies reporting data on the biological effects of clays and zeolites fail to report detailed mineralogical information; hence, it is difficult at present to interpret the biological activities of minerals in terms of their physical and chemical properties. Important mineralogical data that are only rarely considered in biological research include exact mineralogy of the specimen (i.e., identification and abundance of contaminants), physical and chemical properties of minerals, and surface properties of minerals. 141 refs., 1 fig., 8 tabs.

  17. Crystal structure of the NaCa(Fe{sup 2+}, Al, Mn){sub 5}[Si{sub 8}O{sub 19}(OH)](OH){sub 7} {center_dot} 5H{sub 2}O mineral: A new representative of the palygorskite group

    SciTech Connect

    Rastsvetaeva, R. K. Aksenov, S. M.; Verin, I. A.

    2012-01-15

    A specimen of a new representative of the palygorskite-sepiolite family from Aris phonolite (Namibia) is studied by single-crystal X-ray diffraction. The parameters of the triclinic (pseudomonoclinic) unit cell are as follows: a = 5.2527(2) Angstrom-Sign , b = 17.901(1) Angstrom-Sign , c = 13.727(1) Angstrom-Sign , {alpha} = 90.018(3) Degree-Sign , {beta} = 97.278(4) Degree-Sign , and {gamma} = 89.952(3) Degree-Sign . The structure is solved by the direct methods in space group P1-bar and refined to R = 5.5% for 4168 |F| > 7{sigma}(F) with consideration for twinning by the plane perpendicular to y (the ratio of the twin components is 0.52: 0.48). The crystal chemical formula (Z = 1) is (Na{sub 1.6}K{sub 0.2}Ca{sub 0.2})[Ca{sub 2}(Fe{sub 3.6}{sup 2+}Al{sub 1.6}Mn{sub 0.8})(OH){sub 9}(H{sub 2}O){sub 2}][(Fe{sub 3.9}{sup 2+}Ti{sub 0.1})(OH){sub 5} (H{sub 2}O){sub 2}][Si{sub 16}O{sub 38}(OH){sub 2}] {center_dot} 6H{sub 2}O, where the compositions of two ribbons of octahedra and a layer of Si tetrahedra are enclosed in brackets. A number of specific chemical, symmetrical, and structural features distinguish this mineral from other minerals of this family, in particular, from tuperssuatsiaite and kalifersite, which are iron-containing representatives with close unit cell parameters.

  18. Fluorescent minerals, a review

    USGS Publications Warehouse

    Modreski, P.J.; Aumente-Modreski, R.

    1996-01-01

    Fluorescent minerals are more than just an attractive novelty, and collecting them is a speciality for thousands of individuals who appreciate their beauty, rarity, and scientific value. Fluorescent properties can be used as an aid to mineral identification, locality determination, and distinction between natural and synthetic gemstones. This article gives an overview of those aspects of fluorescence that are of most interest to collectors, hobbyists, and mineralogists. -from Authors

  19. [Synthetic mineral fibers].

    PubMed

    Boillat, M A

    1999-03-27

    The group of man-made mineral fibres includes slagwool, glasswool, rockwool, glass filaments and microfibres, as well as refractory ceramic fibres. The toxicity of mineral fibres is determined by several factors such as the diameter (< or = 3-3.5 microns) and the length of the fibres (< 100 microns), their biopersistence, which is much shorter for man-made mineral fibres than for asbestos fibres, their physicochemical structure and surface properties, and the exposure level. The chemical composition of the various types of man-made mineral fibres depends directly on the raw material used to manufacture them. While naturally occurring fibres are crystalline in structure, most man-made mineral fibres are amorphous silicates combined with various metal oxides and additives. Observations using intracavitary administration have provided evidence that some types of man-made mineral fibres are bioactive in cellular and animal experiments and may induce lung tumours and mesothelioma. It is difficult to extrapolate these results to humans since they bypass inhalation, deposition, clearance and translocation mechanisms. Inhalation studies show more realistic results but differences are observed between animal species regarding their sensibility to tumours. There is no firm evidence that exposure to various wools is associated with lung fibrosis, pleural lesions or nonspecific respiratory disease in humans. A possible exception may be mentioned for refractory ceramic fibres. A slightly elevated standard mortality ratio for lung cancer has been documented in large cohorts of workers (USA, Europe and Canada) exposed to man-made mineral fibres, especially in the early technological phase. It is not possible to determine from these data whether the risk of lung cancer is due to the man-made mineral fibres themselves, in particular due to the lack of data on smoking habits. No increased risk of mesothelioma has been demonstrated in these cohorts. Epidemiological data are

  20. Biomineralization of magnetic minerals

    NASA Astrophysics Data System (ADS)

    Moskowitz, Bruce M.

    1995-07-01

    New developments and discoveries in biomineralization have occurred almost continuously in the intervening decade since the previous IUGG quadrennial report on biomineralization and biomagnetism was published [Kirschvink, 1983]. Biomineralization is widespread in the biosphere and over 60 different inorganic minerals are produced by a variety of organisms from bacteria to humans [Lowenstam and Weiner, 1989]. The literature on biomineralization is interdisplinary, combining research in microbiology, biotechnology, physics, geology, and paleomagnetism. For paleomagnetism and rock magnetism, iron biomineralization of magnetic minerals is of prime importance. From a paleomagnetism perspective, biogenic magnetic minerals can be deposited in sediments and acquire a natural remanent magnetization that preserves a record of the ancient geomagnetic field. From a rock magnetism perspective, biogenic magnetic minerals provide novel sources of magnetic material for experimental studies in fine particle magnetism. Both perspectives are interrelated through a common goal of developing magnetic techniques to detect biogenic magnetic minerals in sediments and soils. For example, the extent to which iron biominerals contribute to the fine-grained magnetic mineral assemblages in freshwater and marine sediments is important for identifying and interpreting the magnetic record of environmental change [Oldfield, 1992; Reynolds and King, this issue].

  1. Mineral commodity summaries 2014

    USGS Publications Warehouse

    ,

    2014-01-01

    Each chapter of the 2014 edition of the U.S. Geological Survey (USGS) Mineral Commodity Summaries (MCS) includes information on events, trends, and issues for each mineral commodity as well as discussions and tabular presentations on domestic industry structure, Government programs, tariffs, 5-year salient statistics, and world production and resources. The MCS is the earliest comprehensive source of 2013 mineral production data for the world. More than 90 individual minerals and materials are covered by two-page synopses. For mineral commodities for which there is a Government stockpile, detailed information concerning the stockpile status is included in the two-page synopsis. Abbreviations and units of measure, and definitions of selected terms used in the report, are in Appendix A and Appendix B, respectively. “Appendix C—Reserves and Resources” includes “Part A—Resource/Reserve Classification for Minerals” and “Part B—Sources of Reserves Data.” A directory of USGS minerals information country specialists and their responsibilities is Appendix D. The USGS continually strives to improve the value of its publications to users. Constructive comments and suggestions by readers of the MCS 2014 are welcomed.

  2. Mineral commodity summaries 2013

    USGS Publications Warehouse

    ,

    2013-01-01

    Each chapter of the 2013 edition of the U.S. Geological Survey (USGS) Mineral Commodity Summaries (MCS) includes information on events, trends, and issues for each mineral commodity as well as discussions and tabular presentations on domestic industry structure, Government programs, tariffs, 5-year salient statistics, and world production and resources. The MCS is the earliest comprehensive source of 2012 mineral production data for the world. More than 90 individual minerals and materials are covered by two-page synopses. For mineral commodities for which there is a Government stockpile, detailed information concerning the stockpile status is included in the two-page synopsis. Abbreviations and units of measure, and definitions of selected terms used in the report, are in Appendix A and Appendix B, respectively. “Appendix C—Reserves and Resources” includes “Part A—Resource/Reserve Classification for Minerals” and “Part B—Sources of Reserves Data.” A directory of USGS minerals information country specialists and their responsibilities is Appendix D. The USGS continually strives to improve the value of its publications to users. Constructive comments and suggestions by readers of the MCS 2013 are welcomed.

  3. Minerals: the resource gap

    SciTech Connect

    Velocci, T.

    1980-10-01

    US imports of important non-fuel minerals may have contributed to a false sense of security that could have serious economic and defense consequences. Imports account for over 90 percent of the chromite, manganese ore, and cobalt, and 90 percent of the platinum group metals. The primary sources for many of these minerals are the Soviet Union and Africa, a price and supply vulnerability which rivals Middle East oil and of which the American public is unaware. The Soviet shift to a net minerals importer will intensify competition for minerals and could lead to confrontation. The decline in US mineral production is blamed on escalating costs, largely from regulations, that prevent plant and equipment modernization and land withdrawal policies. A strategic stockpile planned for over 90 materials was established in 1939 for defense purposes, but eratic goals and planning as well as economic changes have kept the plan from being implemented. The first steps of an appropriate policy would promote domestic minerals production and open up Federal lands for exploration and development. (DCK)

  4. Minerals yearbook, 1982. volume 1. metals and minerals

    SciTech Connect

    Not Available

    1984-01-01

    This volume of the Minerals Yearbook, covering metals and minerals, contains 73 commodity or commodity group chapters with data on approximately 90 minerals that were obtained as a result of the mineral information gathering activities of the Bureau of Mines. In addition, the volume contains a chapter on mining and quarrying trends and a statistical summary.

  5. Minerals yearbook, 1983. Volume 1. Metals and minerals

    SciTech Connect

    Not Available

    1984-01-01

    This volume of the Minerals Yearbook, covering metals and minerals, contains 73 commodity or commodity group chapters with data on approximately 90 minerals that were obtained as a result of the mineral information gathering activities of the Bureau of Mines. In addition, the volume contains a chapter on mining and quarrying trends and a statistical summary.

  6. [Sorption and desorption of phenanthrene by organo-mineral complexes with different bridge cations].

    PubMed

    Ni, Jin-zhi; Luo, Yong-ming; Wei, Ran; Li, Xiu-hua; Qian, Wei

    2008-12-01

    Sorption and desorption of phenanthrene by organo-mineral complexes with Ca2+, Fe3+ and Al3+ as bridge cations were studied according to the association type between organic matter and minerals in natural soils. The results showed that the data of phenanthrene sorption and desorption by different cation saturated montmorillonite and their corresponding humic acid and mineral complexes could be fitted with Freundlich model, and the order of the sorption capacities (Kf) were Ca-Mont (0.184) > Fe-Mont (0.028) > Al-Mont (0.015) and Fe-Mont-HA (2.341) > Ca-Mont-HA (1.557) > Al-Mont-HA (1.136), respectively. The Kf values of humic acid and mineral complexes were far greater than those of minerals, which demonstrated that humic acid made great contributions to the sorption of phenanthrene in the organo-mineral complexes. However, the Kf values of the organo-mineral complexes with different bridge cations were not consistent with their organic carbon content, which indicated that both the organic carbon content and the combined types between organic matter and mineral could affect the sorption capacity of phenanthrene by the organo-mineral complexes. The desorption hysteresis of phenanthrene was significant for Ca2+ and Al3+ bridged organo-mineral complexes. Desorption hysteresis of phenanthrene was mainly from the sorption of phenanthrene by organic matter, and the contributions of mineral to the desorption hysteresis were not significant.

  7. Minerals Yearbook, 1989. Volume i. Metals and Minerals

    SciTech Connect

    Not Available

    1989-01-01

    The edition of the Minerals Yearbook discusses the performance of the worldwide mineral industry during 1989 and provides background information to assist in interpreting that performance. Volume I, Metals and Minerals, contains chapters on virtually all metallic and industrial mineral commodities important to the U.S. economy. A chapter on advanced materials also has been added to the Minerals Yearbook series beginning with the 1989 volume. In addition, a chapter on survey methods used in data collection with a statistical summary of nonfuel minerals and a chapter on trends in mining and quarrying in the metals and industrial mineral industries are included.

  8. Minerals yearbook, 1993. Volume 1. Metals and minerals. Annual report

    SciTech Connect

    1993-12-31

    This edition of the Minerals Yearbook discusses the performance of the worldwide minerals and materials industry during 1993 and provides background information to assist in interpreting that performance. It contains chapters on virtually all metallic and industrial mineral commodities important to the U.S. economy. A chapter on survey methods with a statistical summary of nonfuel minerals, and a chapter on trends in mining and quarrying in the metals and industrial mineral industries are also included.

  9. Minerals yearbook, 1994. Volume 1. Metals and minerals. Annual report

    SciTech Connect

    1994-12-31

    The edition of the Minerals Yearbook discusses the performance of the worldwide minerals and materials industry during 1994 and provides background information to assist in interpreting that performance. The volume I, Metals and Minerals, contains chapters on virtually all metallic and industrial mineral commodities important to the U.S. economy. The volume also contains chapters on Survey Methods, a Statistical Summary of Nonfuel Minerals, and Trends in Mining and Quarrying.

  10. The mineral economy of Brazil--Economia mineral do Brasil

    USGS Publications Warehouse

    Gurmendi, Alfredo C.; Barboza, Frederico Lopes; Thorman, Charles H.

    1999-01-01

    This study depicts the Brazilian government structure, mineral legislation and investment policy, taxation, foreign investment policies, environmental laws and regulations, and conditions in which the mineral industry operates. The report underlines Brazil's large and diversified mineral endowment. A total of 37 mineral commodities, or groups of closely related commodities, is discussed. An overview of the geologic setting of the major mineral deposits is presented. This report is presented in English and Portuguese in pdf format.

  11. Measuring the Hardness of Minerals

    ERIC Educational Resources Information Center

    Bushby, Jessica

    2005-01-01

    The author discusses Moh's hardness scale, a comparative scale for minerals, whereby the softest mineral (talc) is placed at 1 and the hardest mineral (diamond) is placed at 10, with all other minerals ordered in between, according to their hardness. Development history of the scale is outlined, as well as a description of how the scale is used…

  12. Animal...Vegetable...or Mineral?

    ERIC Educational Resources Information Center

    Cameron, Eugene

    1973-01-01

    Outlines the problems facing the United States with mineral reserves being depleted, and the consumption of minerals outstripping production. Expresses concern about the deteriorating mineral position, and the ignorance and confusion of the public with respect to mineral production and supply, energy requirements, and environmental consequences.…

  13. American Strategic Minerals

    NASA Astrophysics Data System (ADS)

    DeYoung, John H., Jr.; Chidester, Alfred H.

    American Strategic Minerals is a collection of six papers that were presented in December 1982 at a conference organized by the Center for the Study of Marine Policy at the University of Delaware. According to editor Gerard J. Mangone, director of the center, the papers were commissioned “to investigate not only the objective resource situation, but also past United States policy on strategic minerals and future options open to Washington.” The authors and their chapter titles are John C. Kraft, University of Delaware: “Strategic minerals and world stability” V. Anthony Cammarota, Jr., U.S. Bureau of Mines: “America's dependence on strategic minerals” John D. Morgan, U.S. Bureau of Mines: “Future demands of the United States for strategic minerals” J. Robert Moore, University of Texas: “Alternative sources of strategic minerals from the seabed” Allan I. Mendelowitz and John E. Watson, U.S. General Accounting Office: “U.S. mining investments in developing countries” and James W. Curlin, Nautilus Press: “The political dimensions of strategic minerals.”

  14. Hydrated Minerals in the Martian Southern Highlands

    NASA Astrophysics Data System (ADS)

    Wray, James J.; Seelos, F. P.; Murchie, S. L.; Squyres, S. W.

    2008-09-01

    Hydrated minerals including sulfates, phyllosilicates, and hydrated silica have been observed on the surface of Mars by the orbital near-infrared spectrometers OMEGA and CRISM [1,2]. Global maps from OMEGA [3,4] show that km-scale and larger exposures of these minerals are scattered widely throughout the planet's low and mid latitudes, but are relatively rare. Yet CRISM has found hundreds to thousands of Fe/Mg-phyllosilicate exposures in the highlands of Terra Tyrrhena alone [2], suggesting that smaller exposures may be much more common. To search for such exposures, we have surveyed the browse products from all PDS-released CRISM targeted observations (as of July 2008) across a large fraction of the Southern highlands, including the Noachis, Cimmeria, and Sirenum regions. Sulfates are observed in Noachian-aged terrains in each of these regions, including as far South as -63º latitude, suggesting that sulfate formation may have occurred locally or regionally throughout a large fraction of Martian history. Some of our strongest phyllosilicate detections occur adjacent to inferred chloride-bearing deposits [5] in Terra Sirenum. Also in Sirenum, the D 100 km Columbus crater contains light-toned, hydrated sulfate-bearing layers overlying materials that contain both a kaolin group clay and Fe/Mg-smectite clay, in different locations. However, phyllosilicates do not appear predominantly associated with impact craters in the regions surveyed, in contrast with Terra Tyrrhena [2]. We are currently searching for additional hydrated mineral exposures using CRISM multispectral data, providing further detail on their global distribution and identifying local areas of interest for future focused studies. [1] Bibring, J.-P. et al. (2005) Science 307, 1576-1581. [2] Mustard, J. F. et al. (2008) Nature 454, 305-309. [3] Bibring, J.-P. et al. (2006) Science 312, 400-404. [4] Poulet, F. et al. (2007) Mars 7, Abs. #3170. [5] Osterloo M. M. et al. (2008) Science 319, 1651-1654.

  15. Thorium in mineral products.

    PubMed

    Collier, D E; Brown, S A; Blagojevic, N; Soldenhoff, K H; Ring, R J

    2001-01-01

    Many ores contain low levels of thorium. When these ores are processed, the associated radioactivity can be found in mineral concentrates, intermediates and final products. There is an incentive for industries to remove radioactivity from mineral products to allow the movement and sale of these materials, both nationally and internationally, without the need for licensing. Control of thorium in various products involves the development and optimisation of process steps to be able to meet product specifications. The Australian Nuclear Science and Technology Organisation (ANSTO) has undertaken a range of R & D programmes targeting the treatment of thorium-bearing minerals. This paper discusses the application of a microprobe technique for siting radioactivity in zircon and ilmenite and the problems experienced in measuring the concentrations in solid rare earth products.

  16. Mineral mining installations

    SciTech Connect

    Werner, G.; Wisniewski, P.

    1983-12-15

    A mineral mining installation serves to win mineral by explosive blasting. The installation employs a shuttle conveyor arranged alongside a mineral face. Roof supports stand side-by-side at the side of the conveyor remote from the conveyor. The roof supports are connected to the conveyor through shifting rams and have roof-engageable caps or the like supported on hydraulic props. The pans of the conveyor have upstanding walls at the rear side nearest the roof supports which carry rails at their upper ends. The roof caps have wall components pivoted thereto and hydraulic piston and cylinder units serve to swing the wall components up and down. When explosive blasting takes place the wall components are swung down to engage on the walls of the conveyor pans to form a screen between the winning region and the access region of the working.

  17. Mineral find highlights cruise

    NASA Astrophysics Data System (ADS)

    Katzoff, Judith A.

    Heavy minerals with potential commercial value were discovered last month by the U.S. Geological Survey (USGS) in seafloor deposits off the coasts of Virginia and Georgia. The USGS sent the research vessel J. W. Powell on a 25-day cruise along the East Coast to assess the concentrations of commercially important minerals in that segment of the U.S. Exclusive Economic Zone (EEZ).Assistant Secretary of the Interior Robert Broadbent called the findings of the Powell “promising” and said they served as a “reminder of just how little we do know about the seafloor resources just a few miles offshore.”

  18. Minerals Yearbook 1989: Boron

    SciTech Connect

    Lyday, P.A.

    1990-08-01

    U.S. production and sales of boron minerals and chemicals decreased during the year. Domestically, glass fiber insulation was the largest use for borates, followed by sales to distributors, textile-grade glass fibers, and borosilicate glasses. California was the only domestic source of boron minerals. The United States continued to provide essentially all of its own supply while maintaining a strong position as a source of sodium borate products and boric acid exported to foreign markets. Supplementary U.S. imports of Turkish calcium borate and calcium-sodium borate ores, borax, and boric acid, primarily for various glass uses, continued.

  19. The Perils of Partition: Erroneous Results from Applying D Mineral/Magma to Rocks that Equilibrated Without Magma

    NASA Astrophysics Data System (ADS)

    Treiman, A. H.

    1995-09-01

    10 x CI, no LREE enrichment, and no Eu depletion (Figure 1). The petrogenesis and planetologic implications of this "parent magma" must be fundamentally different from those of the original simple basalt. If the rock equilibrated at a temperature far below its solidus, each mineral species would appear to have had a different parent magma (because of the various temperature dependencies of the Dmineral/mineral(s)). In the above example, using deep-subsolidus Dmineral/mineral [6,7,8] and Dmineral/basalt, one would infer that each mineral had a distinct parent magma, with REE abundances in the order [whitlockite magma] ~? [augite magma] > [opx magma] > [plag magma]. This order looks like, but is not, the order of igneous crystallization. Figure 1: Calculated REE abundances in minerals of a eucrite basalt (CREE = 10 X CI), chemically equilibrated without magma present just below its solidus temperature. Also shown are calculated REE abundances in the "parent magma" that would be inferred by assuming that the mineral compositions reflected equilibration with a magma. References: [1] Jones J. H. (1995) ch. 7, Handbook of Physical Constants, Vol. 3, Chapter 7, AGU. [2] Barnes S. J. (1986) Contrib. Mineral. Petrol., 93, 524-531. [3] Consolmagno G. J. and Drake M. J. (1977) GCA, 41, 1271-1282. [4] Treiman A. H., GCA, submitted. [6] Floss C. (1991) Ph.D. thesis, Washington University, St. Louis, Missouri. [7] Pun A. and Papike J. J. (1994) LPS XXV, 1111-1112. [8] Stosch H.-G. (1982) GCA, 46, 793-811.

  20. Mineral Mapping with AVIRIS and EO-1 Hyperion

    NASA Technical Reports Server (NTRS)

    Kruse, Fred A.

    2004-01-01

    Imaging Spectrometry data or Hyperspectral Imagery (HSI) acquired using airborne systems have been used in the geologic community since the early 1980 s and represent a mature technology (Goetz et al., 1985; Kruse et al., 1999). The solar spectral range, 0.4 to 2.5 m, provides abundant information about many important Earth-surface minerals (Clark et al., 1990). In particular, the 2.0 to 2.5 m (SWIR) spectral range covers spectral features of hydroxyl-bearing minerals, sulfates, and carbonates common to many geologic units and hydrothermal alteration assemblages. Previous research has proven the ability of airborne and spaceborne hyperspectral systems to uniquely identify and map these and other minerals, even in sub-pixel abundances (Kruse and Lefkoff, 1993; Boardman and Kruse, 1994; Boardman et al., 1995; Kruse, et al., 1999). This paper describes a case history for a site in northern Death Valley, California and Nevada along with selected SNR calculations/results for other sites around the world. Various hyperspectral mineral mapping results for this site have previously been presented and published (Kruse, 1988; Kruse et al., 1993, 1999, 2001, 2002, 2003), however, this paper presents a condensed summary of key details for hyperspectral data from 2000 and 2001 and the results of accuracy assessment for satellite hyperspectral data compared to airborne hyperspectral data used as ground truth.

  1. Impact of Particle Generation Method on the Apparent Hygroscopicity of Insoluble Mineral Particles

    SciTech Connect

    Sullivan, Ryan; Moore, Meagan J.; Petters, Markus D.; Kreidenweis, Sonia M.; Qafoku, Odeta; Laskin, Alexander; Roberts, Greg C.; Prather, Kimberly A.

    2010-07-28

    Atmospheric mineral dust particles represent a major component of tropospheric aerosol mass and provide a reactive surface for heterogeneous reactions with trace atmospheric gases (Dentener et al. 1996).Heterogeneous processes alter the chemical balance of the atmosphere and also modify the physicochemical properties of mineral dust particles (Bauer et al. 2004). Organic and inorganic vapors can react with or partition to dust particles and alter their chemical composition (Al-Hosney et al. 2005; Laskin et al. 2005a, 2005b; Liu et al. 2008; Sullivan et al. 2007, 2009a; Sullivan and Prather 2007; Usher et al. 2003). Calcite (CaCO3) is one of the most reactive components of mineral dust, readily reacting with acidic gases. The fraction of CaCO3 in total dust mineralogy displays large variations between desert regions and other regions of the world as well as between individual mineral particles (Claquin et al. 1999; Jeong 2008; Laskin et al. 2005b; Sullivan et al. 2007). Through reactions with acidic gases CaCO3 can be converted to soluble hygroscopic products including CaCl2 and Ca(NO3)2, and sparingly soluble, non-hygroscopic products including CaSO4 and CaC2O4 (Krueger et al. 2004; Liu et al. 2008; Sullivan et al. 2009a, 2009b).

  2. Heterogeneity of Mg Isotopes and Variable ^26Al/^27Al Ratio in FUN CAIs

    NASA Astrophysics Data System (ADS)

    Park, C.; Nagashima, K.; Hutcheon, I. D.; Wasserburg, G. J.; Papanastassiou, D. A.; Davis, A. M.; Huss, G. R.; Krot, A. N.

    2013-09-01

    We report high-precision Mg-isotope data of individual minerals from the Axtell 2271, BG82DH8, EK1-4-1, C1, TE, and CG14 FUN CAIs, which shows variations in both Mg-isotope ratio and ^26Al/^27Al ratio.

  3. Hydrothermal and Diagenetic Mineralization on Mars

    NASA Astrophysics Data System (ADS)

    Ehlmann, B. L.; Quinn, D. P.

    2015-12-01

    Predicted by geophysical modeling, the mineraolgic record of early Mars groundwater has only recently been discovered. First, rover exploration in sedimentary basins reveals diagenesis. At Meridiani, sandstone porosity is occluded by precipitation of secondary sulfates, hematite, and silica. Multiple alteration episodes are indicated by crystal vugs, disruption of preexisting textures by hematite concretions, and grain coatings (e.g. McLennan et al., 2005). At Gale crater, raised ridges in mudstones, interpreted to be early diagenetic features, are crossed by later-emplaced hydrated calcium sulfate veins (e.g. Grotzinger et al., 2014). Waters in Gale were likely circumneutral while jarosite mineralogy at Meridiani implies acidic waters. Second, systems of raised ridges at 100-m scale are observed from orbit in multiple Martian sedimentary rock units. An outstanding example is sulfate-bearing sediments exhumed at the northern margin of the Syrtis Major lavas (e.g. Quinn & Ehlmann, 2015). Polygonal and with no clearly preferred orientation, the ridges rise 5-30 m above the surrounding terrain. Parallel light-toned grooves with dark interiors (indicative of isopachous fills) and jarosite in ridge mineralogy point to mineralization by acidic waters. Third, some mineral assemblages observed from orbit represent the products of subsurface aqueous alteration at elevated temperatures (Ehlmann et al., 2011). These are globally distributed, exposed in scarps and by impact cratering. Mineral assemblages variously include (a) serpentine and carbonate; (b) prehnite and chlorite, and (c) zeolites. Collectively, these datasets indicate that groundwaters were spatially widespread on ancient Mars, contributing to the sustenance of lakes and to the alteration of bedrock to >1 km depths. While the Martian surface may have always been relatively inhospitable, a warmer, wetter subsurface provided a long-term potentially habitable environment. Key outstanding questions remaining include

  4. Novel biological approaches to carbon mineralization

    NASA Astrophysics Data System (ADS)

    Power, Ian; Kenward, Paul; Harrison, Anna; Dipple, Gregory; Raudsepp, Mati; Wilson, Siobhan; Southam, Gordon

    2015-04-01

    supersaturated solutions in tens of days. Precipitates were positively identified as magnesite using transmission electron microscopy and selected area electron diffraction of a thin section produced by focus ion beam milling. These experiments represent an acceleration in magnesite formation of several orders of magnitude in comparison to naturally occurring magnesite at near-surface conditions and without requiring energy input (e.g., high temperature reactions). Our current focus is to further elucidate this reaction pathway and upscale precipitation for sequestering anthropogenic CO2. [1] Power et al. (2013) Rev. Mineral. Geochem. 77: 305-360. [2] Power et al. (2013) Int. J. Greenh. Gas Control. 16: 145-155. [3] Harrison et al. (2013) Environ. Sci. Technol. 47: 126-134. [4] Power et al. (2007) Geochem. Trans. 8, 13. [5] Hänchen et al. (2008) Chem. Eng. Sci. 63: 1012-1028. [6] Roberts et al. (2013) Proc. Natl. Acad. Sci. U.S.A.. 110: 14540-14545. [7] Kenward et al. (2009) Geobiology 7: 556-565.

  5. Mechanisms of primary mineral weathering inferred from B isotopes

    NASA Astrophysics Data System (ADS)

    Voinot, A.; Turpault, M.-P.; Chabaux, F.; Lemarchand, D.

    2012-04-01

    Silicate weathered minerals result from a combination of dissolution/precipitation or transformation reactions. Despite their chemical and isotopic compositions as well as their mineralogy record the physico-chemical conditions of their formation and history, the determination of the current state of weathering in soils still remains very challenging. The main difficulties come from a difficult access to the mineral sites actually active during primary mineral transformation and from non-stoichiometric release of site-forming cations. To better characterize how minerals record the conditions of their formation, we coupled analyses of mineralogy with major elements and boron isotopes in a series of primary minerals (biotite, muscovite, K-feldspar and plagioclase) associated in varying amount with their replacement phases (vermiculite, kaolinite, illite…). The minerals are sampled along an acid Alocrisoil profile developed on granitic bedrock from the Breuil-Chenue forest (France). Previous studies have demonstrated that boron occupies different minerals sites (tetrahedron in substitution of Si, or interfoliar sites possibly in direct contact with the surrounding fluid, Williams et al. 2001, Muttik et al. 2011, Voinot et al., in prep.). Voinot et al. (in prep.) have also demonstrated that boron isotopes are very sensitive to silicate transformation or dissolution reactions. In deeper soil layers (100 to 130 cm), kaolinite is found in biotite mineral habitus. Examination of the boron isotopes distribution in those weathered agglomerates points to a boron depletion and a rapid isotopic equilibration with the surrounding soil solution as kaolinite fraction increases. The same - but magnified - trend is observed during shallow weathering mechanisms (20 to 30 cm) of fine particles of biotite (< 200 µm). By contrast, coarse biotite minerals (> 200 µm) evolve to a vermiculite-like product that tends to be enriched in boron (up to three times the initial biotite

  6. Identification of Minerals

    ERIC Educational Resources Information Center

    Allison, Diane

    2005-01-01

    The lab described in this article was developed to satisfy two major goals. First, the activity is designed to show students the proper techniques used to identify the seven characteristics of all minerals. Second, the lab gives students a glimpse into the life of a professional field geologist. The author has students complete this lab at the end…

  7. New mineral physics panels

    NASA Astrophysics Data System (ADS)

    The AGU Committee on Mineral Physics has formed itself into six panels. The committee chairman is Orson L. Anderson of the Department of Earth and Space Sciences, University of California, Los Angeles; foreign secretary is Robert Liebermann, Department of Earth and Space Sciences, State University of New York, Stony Brook. The six panels are as follows.

  8. Mineral composition of basidiomes of Amanita species.

    PubMed

    Vetter, János

    2005-06-01

    Basidiomes of 43 samples of eight Amanita species were gathered from different habitats of Hungary. The mineral composition (22 elements) was analysed by the ICP method in three independent replications, and mineral compositions found as discussed and compared. The Amanita species analysed were very different in As-, Cd-, Cr-, Mo-, Mn-, Se- and mainly in V-content. Other elements (Al, B, Ba, Ca, Co, Cu, Fe, Mg, Na, Ni, Sr, Ti, Zn) occur in the basidiomes in balanced concentrations. The K and P contents have the lowest differences. Summarizing all the data (n = 43), the average mineral status of species of Amanita can be deduced. The lowest variability measured was for K and P, and the highest for chromium, nickel and vanadium. Specific, significant accumulation was found only for vanadium, due to the previously demonstrated occurrence of a binding molecule 'amavadine' in the basidiomes of A. muscaria. Remarkable Cd-levels were estimated in A. pantherina and A. muscaria (11.4 and 12.3 mg kg(-1) D.M., respectively). The higher contents of other elements (e.g. K, practically in all species; Se in A. strobiliformis) are analytical facts but, not accumulations. The mineral compositions of the ectomycorrhizal genus Amanita, of litter decomposing Agaricus and of wood decaying Trametes were compared. Some significant differences were found (AsAmanita < AsAgaricus; CdAmanita < CdAgaricus; CuAmanita < CuAgaricus; PAmanita KTrametes; PAmanita > PTrametes) but it seems that the mineral composition of the basidiomes is practically independent of the ectomycorrhizal habit. The specificities of the fungi-tree symbiotic interactions are known, and well documented (higher uptake and transport of certain elements first of all of P), however, the differences found in the mineral components are due to other factors (e.g. substrates, accumulating ability) and not to the mycorrhizal status.

  9. Minerals yearbook 1977. Volume I. Metals and minerals

    SciTech Connect

    Not Available

    1980-01-01

    This report contains chapters on virtually all metallic and nonmetallic mineral commodities important to the domestic economy. In addition, it includes a general review chapter on the mineral industries, a chapter on mining and quarrying trends, and a statistical summary.

  10. Minerals yearbook, 1985. Volume 1. Metals and minerals

    SciTech Connect

    Not Available

    1987-01-01

    This volume of the 1985 Minerals Yearbook, covering metals and minerals, contains 72 commodity or commodity group chapters with data on approximately 90 minerals that were obtained as a result of the mineral information gathering activities of the Bureau of Mines. In addition, the volume contains a chapter on mining and quarrying trends, a chapter discussing the statistical surveying methods used by the Bureau of Mines, and a statistical summary.

  11. Minerals yearbook, 1984. Volume 1. Metals and minerals

    SciTech Connect

    Not Available

    1985-01-01

    The volume of the Minerals Yearbook, covering metals and minerals, contains 72 commodity or commodity group chapters with data on approximately 90 minerals that were obtained as a result of the mineral information gathering activities of the Bureau of Mines. In addition, the volume contains a chapter on mining and quarrying trends, a chapter discussing the statistical surveying methods used by the Bureau of Mines, and a statistical summary.

  12. Minerals Yearbook, 1988. Volume 1. Metals and minerals

    SciTech Connect

    Not Available

    1990-01-01

    Volume I of the 1988 Minerals Yearbook, covering metals and minerals, contains 79 commodity or commodity group chapters with data on approximately 90 minerals that were obtained as a result of the mineral information gathering activities of the U.S. Bureau of Mines. In addition, the volume contains chapters on mining and quarrying trends and on the statistical surveying methods used by the Bureau of Mines and a statistical summary.

  13. Adsorption of RNA on mineral surfaces and mineral precipitates

    PubMed Central

    Biondi, Elisa; Furukawa, Yoshihiro; Kawai, Jun

    2017-01-01

    The prebiotic significance of laboratory experiments that study the interactions between oligomeric RNA and mineral species is difficult to know. Natural exemplars of specific minerals can differ widely depending on their provenance. While laboratory-generated samples of synthetic minerals can have controlled compositions, they are often viewed as "unnatural". Here, we show how trends in the interaction of RNA with natural mineral specimens, synthetic mineral specimens, and co-precipitated pairs of synthetic minerals, can make a persuasive case that the observed interactions reflect the composition of the minerals themselves, rather than their being simply examples of large molecules associating nonspecifically with large surfaces. Using this approach, we have discovered Periodic Table trends in the binding of oligomeric RNA to alkaline earth carbonate minerals and alkaline earth sulfate minerals, where those trends are the same when measured in natural and synthetic minerals. They are also validated by comparison of co-precipitated synthetic minerals. We also show differential binding of RNA to polymorphic forms of calcium carbonate, and the stabilization of bound RNA on aragonite. These have relevance to the prebiotic stabilization of RNA, where such carbonate minerals are expected to have been abundant, as they appear to be today on Mars. PMID:28382177

  14. Oxygen Extraction from Minerals

    NASA Technical Reports Server (NTRS)

    Muscatello, Tony

    2017-01-01

    Oxygen, whether used as part of rocket bipropellant or for astronaut life support, is a key consumable for space exploration and commercialization. In Situ Resource Utilization (ISRU) has been proposed many times as a method for making space exploration more cost effective and sustainable. On planetary and asteroid surfaces the presence of minerals in the regolith that contain oxygen is very common, making them a potential oxygen resource. The majority of research and development for oxygen extraction from minerals has been for lunar regolith although this work would generally be applicable to regolith at other locations in space. This presentation will briefly survey the major methods investigated for oxygen extraction from regolith with a focus on the current status of those methods and possible future development pathways. The major oxygen production methods are (1) extraction from lunar ilmenite (FeTiO3) with either hydrogen or carbon monoxide, (2) carbothermal reduction of iron oxides and silicates with methane, and (3) molten regolith electrolysis (MRE) of silicates. Methods (1) and (2) have also been investigated in a two-step process using CO reduction and carbon deposition followed by carbothermal reduction. All three processes have byproducts that could also be used as resources. Hydrogen or carbon monoxide reduction produce iron metal in small amounts that could potentially be used as construction material. Carbothermal reduction also makes iron metal along with silicon metal and a glass with possible applications. MRE produces iron, silicon, aluminum, titanium, and glass, with higher silicon yields than carbothermal reduction. On Mars and possibly on some moons and asteroids, water is present in the form of mineral hydrates, hydroxyl (-OH) groups on minerals, andor water adsorbed on mineral surfaces. Heating of the minerals can liberate the water which can be electrolyzed to provide a source of oxygen as well. The chemistry of these processes, some key

  15. Internal and External Validity Issues with Motivation to Manage Research: A Reply to Miner, Smith, and Ebrahimi.

    ERIC Educational Resources Information Center

    Bartol, Kathryn M.; And Others

    1985-01-01

    Addresses issues of internal and external validity in the Miner et al. motivation to manage research. Discusses difficulties with the scoring manual, possible sex bias in the Miner Sentence Completion Scale, and the fact that Miner's thesis rests on comparisons with a single sample from a single university. (BH)

  16. Mineral oil soluble borate compositions

    SciTech Connect

    Dulat, J.

    1981-09-15

    Alkali metal borates are reacted with fatty acids or oils in the presence of a low hlb value surfactant to give a stable mineral oil-soluble product. Mineral oil containing the borate can be used as a cutting fluid.

  17. Effect of aluminium on dissolved organic matter mineralization in an allophanic and kaolinitic temperate rain forest soil

    NASA Astrophysics Data System (ADS)

    Merino, Carolina; Matus, Francisco; Fontaine, Sebastien

    2016-04-01

    Aluminium (Al) and it influence on the mineralization of dissolved organic matter (DOM) and thus on carbon (C) sequestration in forest soils is poorly understood. We hypothesized that an addition of Al to the soil solution beyond a molar Al:C ratio of 0.1, induces precipitation of the organic matter which leads to an excess Al in the soil solution causing an inhibitory effect for growing microorganisms. We investigated the effect of Al concentrations for the potential of C biodegradation at different Al:C ratios from DOM and Ah mineral soil horizons from two temperate rain forest soils from southern Chile. Dissolved organic matter and surface mineral horizons were incubated with initial molar Al:C ratio from 0.08 to 1.38 found under at field conditions. Mineralization was quantified by measurement of C-CO2 evolved during 15 days. Increasing the initial Al:C ratio > 0.12, led to a considerable reduction in mineralization (up to 70%). For Al:C ratio < 0.12, the mineralization rates from DOM and mineral soils were unaffected. Consequently, there would be a considerable reduction in the biodegradation of DOM and thus an increased in the C sequestration in mineral soils with molar Al:C ratio > 0.12. The observed DOM losses in the stream water of pristine southern forests can be explained by increasing the bioavailability of organic C for Al:C ratio < 0.12. Aluminium concentration had a marked effect at the spectral ART-FTIR bands assigned to cellulose-like and aromatic compounds in Ah mineral soil, diminishing the mineralization. The present results were also confirmed by the Al fluorescence using a confocal microscopy.

  18. Radioactive minerals - Multimedias strategies for their divulgation

    NASA Astrophysics Data System (ADS)

    Cabral, João; Gomes, Ana; Aldano, Ana; Fonseca, Pedro; Cabral, Tiago; Nobre, José

    2014-05-01

    The region corresponding to Sortelha-Penalobo - Bendada, located deep in the transition zone between the Hesperian massif and the Cova da Beira in the central part of Portugal, more specifically in the Mountainous region of the province of Beira Alta, county Sabugal. This region is characterized by great mineral wealth combined with geomorphology of recognized landscape value. Under the scientific point of view, this region is the origin of the mineral sabugalite (HAl(UO2)4(PO4)4.16H2O) that was described by the famous American mineralogist Clifford Frondel (1907-2002) in the fifties of the 20th century. Uranium minerals of Sabugal region were also associated with the radioactivity studies made by the well-known French physicist Marie Curie (1867-1934). In 2007, U. Kolitsch et al described the Bendadaite (Fe (AsO4) 2 (OH) 2 • 4H2O), which corresponds to a new mineral from the group arthurite. The mineral wealth of this region is responsible for a rich history of mining and to highlight the importance until the 1990s the extraction of uranium minerals. The main uranium minerals extracted were the tobernite (Cu (UO2) 2 (PO4) 2 • 12 H2O), the metatobernite (Cu (UO2) 2 (PO4) 2 • 8 H 2 O), the autonite (Ca (UO2) 2 (PO4 ) 2 • 12H2O-10) and sabugalite (HAL (UO2) 4 (PO4) 4 16H2O). Due to the high radioactivity of these minerals, their handling becomes infeasible for disclosure purposes. An integrated and multidisciplinary museological strategy aims to access 3D images by QR codes, using multitouch as the primary means of interaction with the user, and can handle even the virtual samples, access various magnifications and enjoy explanations supplied by a mascot, in a fun way. All this framework and geological environment becomes an asset for the scientific, educational and economic development of the region. On the other hand, it has a vital importance in the context of a strategy of forming a geological park, in the point of view of tourism, research and

  19. Mineral bridges in nacre.

    PubMed

    Checa, Antonio G; Cartwright, Julyan H E; Willinger, Marc-Georg

    2011-12-01

    We confirm with high-resolution techniques the existence of mineral bridges between superposed nacre tablets. In the towered nacre of both gastropods and the cephalopod Nautilus there are large bridges aligned along the tower axes, corresponding to gaps (150-200nm) in the interlamellar membranes. Gaps are produced by the interaction of the nascent tablets with a surface membrane that covers the nacre compartment. In the terraced nacre of bivalves bridges associated with elongated gaps in the interlamellar membrane (>100nm) have mainly been found at or close to the edges of superposed parental tablets. To explain this placement, we hypothesize that the interlamellar membrane breaks due to differences in osmotic pressure across it when the interlamellar space below becomes reduced at an advanced stage of calcification. In no cases are the minor connections between superimposed tablets (<60nm), earlier reported to be mineral bridges, found to be such.

  20. Mixtures and Mineral Reactions

    NASA Astrophysics Data System (ADS)

    Rumble, D.

    The monograph Mixtures and Mineral Reactions contains a large amount of information of value to mineralogists, petrologists, and geochemists. The first four chapters are a succinct account of the thermodynamic description of crystalline solutions. In these early chapters a comparison is made between different mathematical treatments of activitycomposition models, there is a discussion of the unmixing by exsolution of a single solution into two phases, and methods of computing phase equilibria in assemblages of different minerals are given. If the reader is perplexed by the discussion of standard states (cf. Figure 1.3), not to worry. That is a normal condition for anyone forced to choose between equivalent reference frames yet knowing, somewhere down the line, that the choice will ultimately make one's computational life more or less difficult.

  1. Clay Mineral: Radiological Characterization

    SciTech Connect

    Cotomacio, J. G.; Silva, P. S. C.; Mazzilli, B. P

    2008-08-07

    Since the early days, clays have been used for therapeutic purposes. Nowadays, most minerals applied as anti-inflammatory, pharmaceutics and cosmetic are the clay minerals that are used as the active ingredient or, as the excipient, in formulations. Although their large use, few information is available in literature on the content of the radionuclide concentrations of uranium and thorium natural series and {sup 40}K in these clay minerals.The objective of this work is to determine the concentrations of {sup 238}U, {sup 232}Th, {sup 226}Ra, {sup 228}Ra, {sup 210}Pb and {sup 40}K in commercial samples of clay minerals used for pharmaceutical or cosmetic purposes. Two kinds of clays samples were obtained in pharmacies, named green clay and white clay.Measurement for the determination of {sup 238}U and {sup 232}Th activity concentration was made by alpha spectrometry and gamma spectrometry was used for {sup 226}Ra, {sup 228}Ra, {sup 210}Pb and {sup 40}K determination. Some physical-chemical parameters were also determined as organic carbon and pH. The average activity concentration obtained was 906{+-}340 Bq kg{sup -1} for {sup 40}K, 40{+-}9 Bq kg{sup -1} for {sup 226}Ra, 75{+-}9 Bq kg{sup -1} for {sup 228}Ra, 197{+-}38 Bq kg{sup -1} for {sup 210}Pb, 51{+-}26 Bq kg{sup -1} for {sup 238}U and 55{+-}24 Bq kg{sup -1} for {sup 232}Th, considering both kinds of clay.

  2. The Indian Mineral Development Act.

    ERIC Educational Resources Information Center

    Houle, Antoinette

    1986-01-01

    Discusses the objectives of the Indian Mineral Development Act of 1982 (IMDA) and the possible effects it may have on Indian mineral development. Explains how the provisions of IMDA work to provide Indian tribes with greater flexibility for the development and sale of their mineral resources. (ML)

  3. 76 FR 6110 - Conflict Minerals

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-03

    .... 34-63793; File No. S7-40-10] RIN 3235-AK84 Conflict Minerals AGENCY: Securities and Exchange... 1934 (the ``Exchange Act'') and would require any such issuer for which conflict minerals are necessary... that issuer to disclose in the body of its annual report whether its conflict minerals originated...

  4. Major issues in miner health.

    PubMed Central

    Joyce, S

    1998-01-01

    As recently as the last few decades, thousands of miners died in explosions, roof collapses, fires, and floods each year, and lung disease caused by inhaling mineral dusts was ubiquitous. Miners worked virtually unprotected, and were often treated as expendable bodies fulfilling critical roles in this important industry, which in the United States comprises about 5% of the gross domestic product. PMID:9799195

  5. Culture systems: mineral oil overlay.

    PubMed

    Morbeck, Dean E; Leonard, Phoebe H

    2012-01-01

    Mineral oil overlay microdrop is commonly used during in vitro fertilization (IVF) procedures. Though mineral oil appears homogeneous, it is an undefined product that can vary in quality. Here, we describe the history, chemistry, processing, and optimal use of mineral oil for IVF and embryo culture.

  6. Reducing miner absenteeism

    SciTech Connect

    Peters, R.H.; Clingan, M.R.; Randolph, R.F.

    1989-01-01

    The U. S. Bureau of Mines has prepared this report on strategies for maintaining high job attendance among underground coal miners because high absenteeism is a threat to miners' safety and seriously hampers productivity. A substantial number of research studies on the effectiveness of various strategies for reducing absenteeism among the employees of nonmining industries have been reported in the literature. These strategies have aimed at improving job attendance through one or more of the following: (1) improving employment procedures, (2) overcoming problems that adversely affect one's ability to attend work, and (3) increasing miners' motivation to attend work. Many of these strategies appear applicable to the mining industry, and are reviewed in the first half of this report. The second half of this report describes how one could develop and implement a program for maintaining high attendance at underground coal mines. The steps include measuring and evaluating attendance levels, formulating attendance goals and an absenteeism policy, developing and implementing an attendance promotion program and periodically going through the preceding steps (known as recycling).

  7. Biological impact on mineral dissolution: Application of the lichen model to understanding mineral weathering in the rhizosphere

    PubMed Central

    Banfield, Jillian F.; Barker, William W.; Welch, Susan A.; Taunton, Anne

    1999-01-01

    Microorganisms modify rates and mechanisms of chemical and physical weathering and clay growth, thus playing fundamental roles in soil and sediment formation. Because processes in soils are inherently complex and difficult to study, we employ a model based on the lichen–mineral system to identify the fundamental interactions. Fixed carbon released by the photosynthetic symbiont stimulates growth of fungi and other microorganisms. These microorganisms directly or indirectly induce mineral disaggregation, hydration, dissolution, and secondary mineral formation. Model polysaccharides were used to investigate direct mediation of mineral surface reactions by extracellular polymers. Polysaccharides can suppress or enhance rates of chemical weathering by up to three orders of magnitude, depending on the pH, mineral surface structure and composition, and organic functional groups. Mg, Mn, Fe, Al, and Si are redistributed into clays that strongly adsorb ions. Microbes contribute to dissolution of insoluble secondary phosphates, possibly via release of organic acids. These reactions significantly impact soil fertility. Below fungi–mineral interfaces, mineral surfaces are exposed to dissolved metabolic byproducts. Through this indirect process, microorganisms can accelerate mineral dissolution, leading to enhanced porosity and permeability and colonization by microbial communities. PMID:10097050

  8. Minerals yearbook, 1992. Volume 1. Metals and minerals. Annual report

    SciTech Connect

    Not Available

    1992-01-01

    This edition of the Minerals Yearbook discusses the performance of the worldwide mineral and materials industry during 1992 and provides background information to assist in interpreting that performance. Content of the individual Yearbook volumes follows: Volume I, Metals and Minerals, contains chapters on virtually all metallic and industrial mineral commodities important to the U.S. economy. Chapters on advanced materials, nonrenewable organic materials, and nonferrous metals recycling also were added to the Minerals Yearbook series beginning with the 1989, 1990, and 1991 volumes, respectively. A new chapter on materials recycling has been initiated in this 1992 volume. In addition, a chapter on survey methods used in data collection with a statistical summary of nonfuel minerals and a chapter on trends in mining and quarrying in the metals and industrial mineral industries are included.

  9. Minerals yearbook, 1991. Volume 1. Metals and minerals. Annual report

    SciTech Connect

    1991-12-31

    This edition of the Mineral Yearbook discusses the performance of the worlwide minerals and materials industry during 1991 and provides background information to assist in interpreting that performance. Volume 1, Metals and Mineral, contains chapters on virtually all metallic and industrial mineral commodities important to the U.S. economy. Chapters on advanced materials and nonrenewable organic materials also were added to the Minerals Yearbook series beginning with the 1989 and 1990 volumes, respectively. A new chapter on nonferrous metals recycling has been initiated in this 1991 volume. In addition, a chapter on survey methods used in data collection with a statistical summary of nonfuel minerals and a chapter on trends in mining and quarrying in the metals and industrial mineral industries are included.

  10. Raman spectroscopy of garnet-group minerals

    USGS Publications Warehouse

    Mingsheng, P.; Mao, Ho-kwang; Dien, L.; Chao, E.C.T.

    1994-01-01

    The Raman spectra of the natural end members of the garnet-group minerals, which include pyrope, almandine and spessarite of Fe-Al garnet series and grossularite, andradite and uvarovite of Ca-Fe garnet series, have been studied. Measured Raman spectra of these minerals are reasonably and qualitatively assigned to the internal modes, translational and rotatory modes of SiO4 tetrahedra, as well as the translational motion of bivalent cations in the X site. The stretch and rotatory Alg modes for the Fe-Al garnet series show obvious Raman shifts as compared with those for the Ca-Fe garnet series, owing to the cations residing in the X site connected with SiO4 tetrahedra by sharing the two edges. The Raman shifts of all members within either of the series are attributed mainly to the properties of cations in the X site for the Fe-Al garnet series and in the Y site for the Ca-Fe garnet series. ?? 1994 Institute of Geochemistry, Chinese Academy of Sciences.

  11. AL Amyloidosis

    PubMed Central

    2012-01-01

    Definition of the disease AL amyloidosis results from extra-cellular deposition of fibril-forming monoclonal immunoglobulin (Ig) light chains (LC) (most commonly of lambda isotype) usually secreted by a small plasma cell clone. Most patients have evidence of isolated monoclonal gammopathy or smoldering myeloma, and the occurrence of AL amyloidosis in patients with symptomatic multiple myeloma or other B-cell lymphoproliferative disorders is unusual. The key event in the development of AL amyloidosis is the change in the secondary or tertiary structure of an abnormal monoclonal LC, which results in instable conformation. This conformational change is responsible for abnormal folding of the LC, rich in β leaves, which assemble into monomers that stack together to form amyloid fibrils. Epidemiology AL amyloidosis is the most common type of systemic amyloidois in developed countries with an estimated incidence of 9 cases/million inhabitant/year. The average age of diagnosed patients is 65 years and less than 10% of patients are under 50. Clinical description The clinical presentation is protean, because of the wide number of tissues or organs that may be affected. The most common presenting symptoms are asthenia and dyspnoea, which are poorly specific and may account for delayed diagnosis. Renal manifestations are the most frequent, affecting two thirds of patients at presentation. They are characterized by heavy proteinuria, with nephrotic syndrome and impaired renal function in half of the patients. Heart involvement, which is present at diagnosis in more than 50% of patients, leading to restrictive cardiopathy, is the most serious complication and engages prognosis. Diagnostic methods The diagnosis relies on pathological examination of an involved site showing Congo red-positive amyloid deposits, with typical apple-green birefringence under polarized light, that stain positive with an anti-LC antibody by immunohistochemistry and/or immunofluorescence. Due to the

  12. Enzymatic mineralization of silk scaffolds.

    PubMed

    Samal, Sangram K; Dash, Mamoni; Declercq, Heidi A; Gheysens, Tom; Dendooven, Jolien; Van Der Voort, Pascal; Cornelissen, Ria; Dubruel, Peter; Kaplan, David L

    2014-07-01

    The present study focuses on the alkaline phosphatase (ALP) mediated formation of apatitic minerals on porous silk fibroin protein (SFP) scaffolds. Porous SFP scaffolds impregnated with different concentrations of ALP are homogeneously mineralized under physiological conditions. The mineral structure is apatite while the structures differ as a function of the ALP concentration. Cellular adhesion, proliferation, and colonization of osteogenic MC3T3 cells improve on the mineralized SFP scaffolds. These findings suggest a simple process to generate mineralized scaffolds that can be used to enhanced bone tissue engineering-related utility.

  13. Low bone mineral density among young healthy adult Saudi women

    PubMed Central

    Zeidan, Zeidan A.; Sultan, Intisar E.; Guraya, Shaista S.; Al-Zalabani, Abdulmohsen H.; Khoshhal, Khalid I.

    2016-01-01

    Objectives: To screen for low bone mineral density among young adult Saudi women using quantitative ultrasound (QUS) and exploring the high risk groups. Methods: A cross-sectional study was performed on 279, 20-36 years old female students and employees of Taibah University, Al Madinah Al Munawwarah, Kingdom of Saudi Arabia between January and May 2014. The study included bone status assessed using QUS, a structured self-reported questionnaire, anthropometric measurements, and evaluation of bone markers of bone metabolism. Results: The prevalence of low bone mineral density was 9%. Serum osteocalcin was found significantly higher in candidates with low bone mineral density, 20.67 ng/ml versus 10.7 ng/ml, and it was negatively correlated with T-scores. At any given point in time the exposed subjects to low calcium intake and inadequate sun exposure in the population were 11 times and 3 times more likely to have low bone mineral density, (adjusted odds ratio [OR], 11.0; 95%confidence interval [CI]=3.16, 38.34; p=0.001) and (adjusted OR, 3.32, 95%CI=1.27, 8.66, p<0.01). Conclusion: Early detection screening programs for low bone mineral density are needed in Saudi Arabia as it affects young Saudi women specially the high-risk group that includes young women with insufficient calcium intake and insufficient sun exposure. Serum osteocalcin as a biomarker for screening for low bone mineral density could be introduced. PMID:27761561

  14. Water, mineral waters and health.

    PubMed

    Petraccia, Luisa; Liberati, Giovanna; Masciullo, Stefano Giuseppe; Grassi, Marcello; Fraioli, Antonio

    2006-06-01

    The authors focus on water resources and the use of mineral waters in human nutrition, especially in the different stages of life, in physical activity and in the presence of some morbid conditions. Mineral water is characterized by its purity at source, its content in minerals, trace elements and other constituents, its conservation and its healing properties recognized by the Ministry of Health after clinical and pharmacological trials. Based on total salt content in grams after evaporation of 1l mineral water dried at 180 degrees C (dry residues), mineral waters can be classified as: waters with a very low mineral content, waters low in mineral content, waters with a medium mineral content, and strongly mineralized waters. Based on ion composition mineral waters can be classified as: bicarbonate waters, sulfate waters, sodium chloride or saltwater, sulfuric waters. Based on biological activity mineral waters can be classified as: diuretic waters, cathartic waters, waters with antiphlogistic properties. Instructions for use, doses, and current regulations are included.

  15. Systems genetics of mineral metabolism.

    PubMed

    Fleet, James C; Replogle, Rebecca; Salt, David E

    2011-03-01

    Minerals are essential and toxic elements that have an impact on human health. Although we have learned a tremendous amount about the metabolism, biological roles, and health effects of minerals with the tools of biochemistry, cell biology, and molecular genetics, there are gaps in our knowledge of mineral biology that will benefit from new approaches. Forward genetics, whereby variations in phenotypes are mapped to natural genetic variation in the genome, has been successfully used to increase our understanding of many biologically important traits but has not yet been used extensively for mineral metabolism. In addition, the well-appreciated existence of interactions between minerals justifies a broader, systems approach to the study of mineral metabolism, i.e., ionomics. This short review will explain the value of forward genetics and ionomics as tools for exploring mammalian mineral metabolism.

  16. Electron microprobe mineral analysis guide

    NASA Technical Reports Server (NTRS)

    Brown, R. W.

    1980-01-01

    Electron microprobe mineral analysis guide is a compilation of X-ray tables and spectra recorded from various mineral matrices. Spectra were obtained using electron microprobe, equipped with LiF geared, curved crystal X-ray spectrometers, utilizing typical analytical operating conditions: 15 Kv acceleration potential, 0.02 microampere sample current as measured on a clinopyroxene standard (CP19). Tables and spectra are presented for the majority of elements, fluorine through uranium, occurring in mineral samples from lunar, meteoritic and terrestrial sources. Tables for each element contain relevant analytical information, i.e., analyzing crystal, X-ray peak, background and relative intensity information, X-ray interferences and a section containing notes on the measurement. Originally intended to cover silicates and oxide minerals the tables and spectra have been expanded to cover other mineral phases. Electron microprobe mineral analysis guide is intended as a spectral base to which additional spectra can be added as the analyst encounters new mineral matrices.

  17. Hearing protection for miners

    SciTech Connect

    Schulz, T.

    2008-10-15

    A NIOSH analysis showed that at age 50 approximately 90% of coal miners have a hearing impairment, yet noise included hearing loss is 100% preventable. The article discusses requirements of the MSHA regulations, 30 CFR Part 62 - occupational noise exposure (2000) and a 2008-MSHA document describing technologically achievable and promising controls for several types of mining machinery. Hearing protection is still required for exposure to greater than 90 dBA. These are now commercially available ways to determine how much attenuation an individual gets from a given hearing protector, known as 'fit testing'. 3 refs., 1 fig., 1 tab., 1 photo.

  18. Mineral mining installation

    SciTech Connect

    Plevak, L.; Weirich, W.

    1982-04-20

    A longwall mineral mining installation has a longwall conveyor and a plurality of roof support units positioned side-by-side at the goaf side of the conveyor. The hydraulic appliances of the roof support units, such as their hydraulic props, hydraulic advance rams and hydraulic control valves, are supplied with pressurized hydraulic fluid from hydraulic supply lines which run along the goaf side of the conveyor. A plurality of flat, platelike intermediate members are provided at the goaf side of the conveyor. These intermediate members are formed with internal ducts for feeding the hydraulic fluid from the supply lines to the hydraulic appliances of the roof support units.

  19. Recommended nomenclature for zeolite minerals: report of the subcommittee on zeolites of the International Mineralogical Association, Commission of New Minerals and Mineral Names

    USGS Publications Warehouse

    Coombs, D.S.; Alberti, A.; Armbruster, T.; Artioli, G.; Colella, C.; Galli, E.; Grice, Joel D.; Liebau, F.; Mandarino, J.A.; Minato, H.; Nickel, E.H.; Passaglia, E.; Peacor, D.R.; Quartieri, S.; Rinaldi, R.; Ross, M.; Sheppard, R.A.; Tillmanns, E.; Vezzalini, G.

    1998-01-01

    This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association Commission of New Minerals and Mineral Names. In a working definition of a zeolite mineral used for review, interrupted tetrahedral framework structures are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is allowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundance in atomic proportions. To name these, the appropriate chemical symbol is attached by a hyphen to the series name as a suffix except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely on Si:Al ratio except for heulandite (Si:Al < 4.0) and clinoptilolite (Si:Al ??? 4.0). Dehydration, partial hydration, and over-hydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of a zeolite. Newly recognized species in compositional series are as follows: brewsterite-Sr.-Ba: chabazite-Ca.-Na.-K; clinoptilolite-K, -Na, -Ca: dachiardite-Ca, -Na; erionite-K, -Ca: faujasite-Na, -Ca, -Na: paulingite-K. -Ca; phillipsite-Na, -Ca, -Ka; stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data. IZA structure-type symbols, space-group symmetry; unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species, and three of doubtful status. Herschelite, leonhardite, svetlozarite, and wellsite are discredited as mineral species names. Obsolete and

  20. Fe-Impregnated Mineral Colloids for Peroxide Activation: Effects of Mineral Substrate and Fe Precursor.

    PubMed

    Li, Yue; Machala, Libor; Yan, Weile

    2016-02-02

    Heterogeneous iron species at the mineral/water interface are important catalysts for the generation of reactive oxygen species at circumneutral pH. One significant pathway leading to the formation of such species arises from deposition of dissolved iron onto mineral colloids due to changes in redox conditions. This study investigates the catalytic properties of Fe impregnated on silica, alumina, and titania nanoparticles (as prototypical mineral colloids). Fe impregnation was carried out by immersing the mineral nanoparticles in dilute Fe(II) or Fe(III) solutions at pH 6 and 3, respectively, in an aerobic environment. The uptake of iron per unit surface area follows the order of nTiO2 > nAl2O3 > nSiO2 for both types of Fe precursors. Impregnation of mineral particles in Fe(II) solutions results in predominantly Fe(III) species due to efficient surface-mediated oxidation. The catalytic activity of the impregnated solids to produce hydroxyl radical (·OH) from H2O2 decomposition was evaluated using benzoic acid as a probe compound under dark conditions. Invariably, the rates of benzoic acid oxidation with different Fe-laden particles increase with the surface density of Fe until a critical density above which the catalytic activity approaches a plateau, suggesting active Fe species are formed predominantly at low surface loadings. The critical surface density of Fe varies with the mineral substrate as well as the aqueous Fe precursor. Fe impregnated on TiO2 exhibits markedly higher activity than its Al2O3 and SiO2 counterparts. The speciation of interfacial Fe is analyzed with diffuse reflectance UV-vis analysis and interpretation of the data in the context of benzoic oxidation rates suggests that the surface activity of the solids for ·OH generation correlates strongly with the isolated (i.e., mononuclear) Fe species. Therefore, iron dispersed on mineral colloids is a significant form of reactive iron surfaces in the aquatic environment.

  1. Spectroscopic characterization of manganese minerals.

    PubMed

    Lakshmi Reddy, S; Padma Suvarna, K; Udayabhaska Reddy, G; Endo, Tamio; Frost, R L

    2014-01-03

    Manganese minerals ardenite, alleghanyite and leucopoenicite originated from Madhya Pradesh, India, Nagano prefecture Japan, Sussex Country and Parker Shaft Franklin, Sussex Country, New Jersey respectively are used in the present work. In these minerals manganese is the major constituent and iron if present is in traces only. An EPR study of on all of the above samples confirms the presence of Mn(II) with g around 2.0. Optical absorption spectrum of the mineral alleghanyite indicates that Mn(II) is present in two different octahedral sites and in leucophoenicite Mn(II) is also in octahedral geometry. Ardenite mineral gives only a few Mn(II) bands. NIR results of the minerals ardenite, leucophoenicite and alleghanyite are due to hydroxyl and silicate anions which confirming the formulae of the minerals.

  2. Mineral Time Capsules on Mars?

    NASA Technical Reports Server (NTRS)

    Schirber, Michael

    2006-01-01

    Like dinosaur-age insects trapped in amber, biomolecules sequestered in million-year-old sulfate minerals could provide a glimpse into the past, say researchers who've recently analyzed such minerals from N orth America. The same minerals have recently been discovered on Mars , so they may be a good place to look for traces of past life on the red planet, the researchers say.

  3. Microelectrophoresis of selected mineral particles

    NASA Technical Reports Server (NTRS)

    Herren, B. J.; Tipps, R. W.; Alexander, K. D.

    1982-01-01

    Particle mobilities of ilmenite, labradorite plagioclase, enstatite pyroxene, and olivine were measured with a Rank microelectrophoresis system to evaluate indicated mineral separability. Sodium bicarbonate buffer suspension media with and without additives (0.0001 M DTAB and 5 percent v/v ethylene glycol) were used to determine differential adsorption by mineral particles and modification of relative mobilities. Good separability between some minerals was indicated; additives did not enhance separability.

  4. Clay minerals for advanced ceramics

    SciTech Connect

    Murray, H.H. )

    1989-11-01

    The author describes new and improved beneficiation techniques available to allow the production of clay minerals of exceptionally high purity. This is particularly true for kaolins and smectites. Wet processing techniques include particle size separation, high intensity magnetic separation, chemical leaching, flotation, and selective flocculation. The blending of clay minerals with other minerals provides opportunities to make special ceramic materials such as cordierite and other minerals that have very special ceramic properties including low heat expansion, high fired strength, low absorption, and other desired qualities.

  5. New AGU mineral physics committee

    NASA Astrophysics Data System (ADS)

    Bell, Peter M.

    A new Committee on Mineral Physics consisting of Orson Anderson (chairman), Peter Bell, Raymond Jeanloz, Robert Lieberman, Murli Manghnani, Alexandra Navrotsky, Tom Shankland, Joseph E. Smith, and Donald Weidner has been approved by the AGU Executive Committee.The increasing number of research groups in an area that combines the study of mineral properties and solid state sciences (materials research) created the impetus for this new committee. At AGU meetings, mineral physics studies have been included in recent years in sessions of Volcanology, Petrology, and Geochemistry and sessions of Tectonophysics. A portion of the charter for the new committee includes arranging special sessions for mineral physics that would bridge the two sections.

  6. Minerals Bill introduced in House

    NASA Astrophysics Data System (ADS)

    Richman, Barbara T.

    A bill that aims to strengthen a national minerals policy and to establish a three-member White-House-level council to coordinate the development of this policy was introduced in the House of Representatives on April 30 by James D. Santini (D-Nev.). Entitled the National Minerals Security Act (NMSA), the legislation, if passed, also would amend tax laws to assist the mining industry to make capital investments to locate and produce strategic minerals; it would provide the means for the Secretary of the Interior to make withdrawn public lands available for mineral development; and it would create a revolving fund for the sale and purchase of strategic minerals.Santini estimates that 4 billion tons of minerals are needed annually to sustain the nation's economy. Much of the minerals are supplied by other nations, however; Santini wants to see an end to the United States' dependence on foreign countries, especially those that seem relatively unstable politically. ‘The U.S. has placed its national security in the hands of a few foreign nations,’ Santini said in a recent press conference. ‘We are heavily dependent on the region of southern Africa for 76% of our cobalt, 93% of our platinum, 48% of our chromium, and a host of other strategic and critical minerals. Without these minerals, we cannot build jet aircraft, weapons, or other military hardware vitally important to our national security.’

  7. Mineralization by nanobacteria

    NASA Astrophysics Data System (ADS)

    Kajander, E. Olavi; Bjorklund, Michael; Ciftcioglu, Neva

    1998-07-01

    Nanobacteria are the smallest cell-walled bacteria, only recently discovered in human and cow blood and in commercial cell culture serum. In this study, we identified with energy-dispersive x-ray microanalysis and chemical analysis that all growth phases of nanobacteria produce biogenic apatite on their cell envelope. Fourier transform IR spectroscopy revealed the mineral as carbonate apatite. Previous models for stone formation have lead to a hypothesis that an elevated pH due to urease and/or alkaline phosphatase activity are important lithogenic factors. Our results indicate that carbonate apatite can be formed without these factors at pH 7.4 at physiological phosphate and calcium concentrations. Due to their specific macromolecules, nanobacteria can produce apatite very efficiency in media mimicking tissue fluids and glomerular filtrate and rapidly mineralizing most of available calcium and phosphate. This can be also monitored by (superscript 85)Sr incorporation and provides a unique model for in vitro studies on calcification. Recently, bacteria have been implicated in the formation of carbonate (hydroxy)fluorapatite in marine sediments. Apatite grains are found so commonly in sedimentary rocks that apatite is omitted in naming the stone. To prove that apatite and other minerals are formed by bacteria would implicate that the bacteria could be observed and their actions followed in stones. We have started to approach this in two ways. Firstly, by the use of sensitive methods for detecting specific bacterial components, like antigens, muramic acid and nucleic acids, that allow for detecting the presence of bacteria and, secondly, by follow-up of volatile bacterial metabolites observed by continuous monitoring with ion mobility spectrometry, IMCELL, working like an artificial, educatable smelling nose. The latter method might allow for remote real time detection of bacterial metabolism, a signature of life, in rocks via fractures of drillholes with or without

  8. Thermodynamic properties of minerals

    USGS Publications Warehouse

    Robie, Richard A.

    1962-01-01

    In the ten years since the publication of the national Bureau of Standards comprehensive tables of thermochemical properties, by Rossini and other (1952), a very large body of modern calorimetric and equilibrium data has become available. Because of the complex interrelations among many thermochemical data and the necessity for internal consistency among these values, a complete revision of this standard reference is required. This is also true of the summaries of thermochemical data for the sulfides (Richardson and Jeffes 1952) and for the oxides (Coughlin 1954). The following tables present critically selected values for the heat and free energy of formation, the logarithm of the equilibrium constant of formation Log Kf, the entropy and the molar volume, at 298.15°K (25.0°C) and one atmosphere for minerals.

  9. The minerals of milk.

    PubMed

    Gaucheron, Frédéric

    2005-01-01

    The salt of milk constitutes a small part of milk (8-9 g.L(-1)); this fraction contains calcium, magnesium, sodium and potassium for the main cations and inorganic phosphate, citrate and chloride for the main anions. In milk, these ions are more or less associated between themselves and with proteins. Depending on the type of ion, they are diffusible (cases of sodium, potassium and chloride) or partially associated with casein molecules (cases of calcium, magnesium, phosphate and citrate), to form large colloidal particles called casein micelles. Today, our knowledge and understanding concerning this fraction is relatively complete. In this review, the different models explaining (i) the nature and distribution of these minerals (especially calcium phosphate) in both fractions of milk and (ii) their behaviour in different physico-chemical conditions, are discussed.

  10. The Mineral Physics Committee

    NASA Astrophysics Data System (ADS)

    Mineral Physics Committee members for the period July 1, 1986, to J ne 30, 1988, have been announced. They are Murli H. Manghnani (Hawaii Institute of Geophysics, Honolulu), and Orson L. Anderson (University of California, Los Angeles), Thomas J. Ahrens (California Institute of Technology, Pasadena, Calif.), Subir K. Banerjee (University of Minnesota, Minneapolis), William A. Bassett (Cornell University, Ithaca, N.Y.), Gordon E. Brown, Jr. (Stanford University, Stanford, Calif.), Michael Brown (University of Washington, Seattle), Robert M. Hazen (Geophysical Laboratory, Washington, D.C.), Raymond F. Jeanloz (University of California, Berkeley), Robert C. Liebermann (State University of New York (SUNY),(Stony Brook), Alexandra Navrotsky (Princeton University, Princeton, N.J.), Robert N. Schock (Lawrence Livermore National Laboratory, Livermore, Calif.), and Donald J. Weidner (SUNY Stony Brook).

  11. The Brazilian mineral resources

    NASA Astrophysics Data System (ADS)

    Beurlen, Hartmut; Cassedanne, Jacques Pierre

    1981-04-01

    The activity of the first generation of Brazilian geologists began in the early sixties. Systematic exploration work since then has evidenced some important new mineral reserves in Brazil. The most important examples are the 18 × 10 9 tons of high-grade iron ore (Carajás District), formed by supergene enrichment on iron formations older than 1800 m.y., the 2.5 × 10 9 tons of bauxite and similar reserves of kaolinite as residual enrichment in Cenozoic sediments in the Amazonas Basin (Oriximina, Capim); the potash and magnesium-rich evaporites near Aracajú(Sergipe); the large residual concentrations of phosphate, anatase, pyrochlore and rare earths related to Cretaceous alkaline complexes with carbonatites; and some garnierite and asbestos deposits related to ultramafic rocks in the states of Goiás and Piauí.

  12. Minerals yearbook, 1988: Thorium

    SciTech Connect

    Hedrick, J.B.

    1988-01-01

    Mine production of monazite, the principal source of thorium, decreased slightly in 1988. Associated Minerals (USA) Inc. was the only domestic monazite producer. Monazite produced in the United States was exported, and the thorium products used domestically were derived from imported materials, existing company stocks, and thorium nitrate released from the National Defense Stockpile. Major nonenergy uses were in refractory applications, ceramics, and mantles for incandescent lanterns. The only energy use of thorium in the United States was in the high-temperature gas-cooled (HTGC) nuclear reactor at Fort St. Vrain, CO. Topics discussed in the report include domestic data coverage, legislation and government programs, domestic production, consumption and uses, stocks, prices, foreign trade, world capacity, and world review--(Australia, Brazil, Madagascar, Mozambique).

  13. Protein- mediated enamel mineralization

    PubMed Central

    Moradian-Oldak, Janet

    2012-01-01

    Enamel is a hard nanocomposite bioceramic with significant resilience that protects the mammalian tooth from external physical and chemical damages. The remarkable mechanical properties of enamel are associated with its hierarchical structural organization and its thorough connection with underlying dentin. This dynamic mineralizing system offers scientists a wealth of information that allows the study of basic principals of organic matrix-mediated biomineralization and can potentially be utilized in the fields of material science and engineering for development and design of biomimetic materials. This chapter will provide a brief overview of enamel hierarchical structure and properties as well as the process and stages of amelogenesis. Particular emphasis is given to current knowledge of extracellular matrix protein and proteinases, and the structural chemistry of the matrix components and their putative functions. The chapter will conclude by discussing the potential of enamel for regrowth. PMID:22652761

  14. Mineral Detector for Igneous Rocks

    NASA Astrophysics Data System (ADS)

    Ishikawa, S. T.; Hart, S. D.; Gulick, V. C.

    2010-12-01

    We present a Raman spectral analysis tool that uses machine learning algorithms to classify pure minerals in igneous rocks. Experiments show greater than 90% accuracy classifying a test set of pure minerals against a database of similar reference minerals using an artificial neural network. Efforts are currently underway to improve this tool for use as a mineral detector in rock samples, an important milestone toward autonomously classifying rocks based on spectral, and previous imaging work. Although pure mineral classification has been widely successful, applying the same methods to rocks is difficult because the spectra may represent a combination of multiple, and often competing, mineral signatures. In such cases some minerals may appear with more intensity than others resulting in masking of weaker minerals. Furthermore, with our particular spectrometer (852 nm excitation, ~50 micron spot size), minerals such as potassium feldspar fluoresce, both obscuring its characteristic Raman features and suppressing those of weaker minerals. For example, plagioclase and quartz, two key minerals for determining the composition of igneous rocks, are often hidden by minerals such as potassium feldspar and pyroxene, and are consequently underrepresented in the spectral analysis. These technicalities tend to skew the perceived composition of a rock from its actual composition. Despite these obstacles, an experiment involving a training set of 26 minerals (plagioclase, potassium feldspar, pyroxene, olivine, quartz) and a test set of 57 igneous rocks (basalt, gabbro, andesite, diorite, dacite, granodiorite, rhyolite, granite) shows that generalizations derived from their spectral data are consistent with expected trends: as rock composition goes from felsic to mafic there is a marked increase in the detection of minerals such as plagioclase and pyroxene along with a decrease in the detection of minerals such as quartz and potassium feldspar. The results suggest that phaneritic

  15. [Species Determination and Spectral Characteristics of Swelling Clay Minerals in the Pliocene Sandstones in Xinghai, Qinghai].

    PubMed

    Wang, Chao-wen; Chen, Jiang-jun; Fang, Qian; Yin, Ke; Hong, Han-lie

    2015-10-01

    X-ray diffraction (XRD) and Fourier infrared absorption spectroscopy (FTIR) were conducted to deepen our research on specific species and spectral characteristics of swelling clay minerals in the Pliocene sandstones in Xinghai, Qinghai province. XRD results show that swelling clay minerals are dominant clay minerals in the sandstones, which can be up to 97% in percentage. XRD patterns show 060 reflections of the samples occur both remarkably at 1.534 Å and 1.498 Å, indicating the samples contain physical mixtures of trioctahedral and dioctahedral swelling clay minerals, respectively. Further treatment of Li-300 degrees C heat and glycerol saturation shows the swelling clay minerals collapse to 9.3-9.9 Å with a partial expansion to -18 Å. This indicates the swelling clay minerals dominate montmorillonite and contain minor saponite. The montmorillonite shows no swelling after Li-300 degrees C heat and glycerol saturation because of Li+ inserting into the octahedral layers, which balances the layer charge caused by the substitution of Mg to Al. FTIR results show the samples are composed of a kind of phyllosilicate with absorbed and structural water, which is in agreement with the results of XRD. Absorbed peaks at 913, 842, 880 cm(-1), corresponding to OH associated with Al-Al, Al-Mg, and Al-Fe pairs, further indicates the minerals are dominant dioctahedron in structure. Meanwhile, absorbed peaks at 625 and 519 cm(-1), corresponding to coupled Si-O and Al-O-Si deformation, indicates parts of Si is replaced by Al in tetrahedron. The spectral characteristics of the samples are against the presence of beidellite and nontronite based on the results of XRD and FTIR, while demonstrating an,existence of montmorillonite. This study, to distinguish the specific species of swelling clay species in clay minerals, would be of great importance when using clay mineralogy to interpret provenance and climatic information.

  16. Scientific basis for creation of construction materials based on titanium and alumina minerals

    NASA Astrophysics Data System (ADS)

    Kotova, O.; Shmakova, A.; Ponaryadov, A.

    2017-02-01

    Currently there is a need in affordable and accessible materials with specific physical and chemical properties. Al- and Ti-minerals are excellent test objects for correlation between structure and physical properties of mineral. For example, corundum and ilmenite are related to the same structural type (rhombohedral lattice R3) and possess various physical properties. With the help of modern equipment we studied titanium- and aluminum-containing concentrates of natural raw and also products of various kinds of influences on them, which showed signs of nanostructuring. We observed methods of directional change of physical and chemical characteristics of Al- and Ti-minerals and creation of new commercial products.

  17. A Retrievable Mineral Microcosm for Examining Microbial Colonization and Mineral Precipitation at Seafloor Hydrothermal Vents

    NASA Astrophysics Data System (ADS)

    Dunn, E. E.; Holloway, J. R.; Cary, S.; Voglesonger, K. M.; Ashbridge, D. A.; O'Day, P. A.

    2002-12-01

    Although seafloor hydrothermal vent environments are known to support thriving ecosystems, the microscale physical and chemical environment suitable for microbial colonization and the identity of pioneering organisms is unknown. Because of the fragility of young chimneys and their ephemeral nature, novel methods for sample retrieval and analysis are required. The mineral microcosm consists of four titanium mesh chambers containing crushed minerals mounted on a titanium base that allows for fluid flow through the chambers. The chambers can be filled with different minerals or mineral mixtures (or no minerals) to supply different substrates for microbial colonization and different local microenvironments as minerals react with the surrounding fluids. The device sets on top of an active hydrothermal vent for a period of days to weeks to allow colonization and mineral reaction. The mineral microcosm was deployed during the Atlantis/Alvin Extreme 2001 Cruise (Oct.- Nov.,2001) to 9° 50'N on the East Pacific Rise a total of three times, for ~ 24, ~ 96, and ~ 48 hours each. It was deployed in two different environments, twice in lower temperature (<300°C), diffuse-flow environments and once (for ~96 hours) in a higher temperature black smoker environment (>350°C).Seed minerals included sulfides, sulfates, magnetite, apatite, and quartz, both individually and in mixtures. In the first 24-hour deployment, dissolution of anhydrite but not sulfide minerals within the chambers indicated high temperatures in chamber interiors and rapid reaction rates. Temperatures measured on chamber exteriors before retrieval ranged from 4° -98°C. The 96-hour deployment on a hot vent (fluid ~370°C before deployment) resulted in extensive mineral precipitation and chimney growth inside the mineral chambers, on the outer surfaces of the chambers, and on the platform as a whole, creating micro-chimneys several centimeters tall. The young chimneys were mainly composed of pyrite with lesser

  18. From Mountain Men to Miners.

    ERIC Educational Resources Information Center

    Stevens, Robert L.; Fogel, Jared A.

    1999-01-01

    Examines three of the changes wrought by coal mining: (1) the miner's working conditions; (2) the establishment of company towns; and (3) the violence that ensued when miners from Harlan County, Kentucky, referred to as "Bloody Harlan," tried to better their lives by joining labor unions. (CMK)

  19. Minerals From the Marine Environment

    NASA Astrophysics Data System (ADS)

    Cruickshank, Michael J.

    The current interest in minerals centering on, among other things, potential shortages, long-term needs, and deep seabed nodules, accentuates the usefulness and timeliness of this little book authored by a former chairman of the British National Environmental Research Council.In less than 100 pages, the author puts into perspective the potential for producing minerals from offshore areas of the world. After introducing the reader to the ocean environment and the extraordinary variety of the nature of the seabed, the author describes in some detail the variety of minerals found there. This is done in seven separate chapters entitled ‘Bulk and Non-Metallic Minerals From the Seas’ ‘Metals From the Shallow Seas’ ‘Metals From the Deep Oceans’ ‘Minerals From Solution’ ‘Oil and Gas from the Shallow Seas’ ‘Oil and Gas From Deep Waters’ and ‘Coal Beneath the Sea.’ The remaining chapters give a brief regional review of marine minerals distribution for eight areas of significant socioeconomic structure, and a short recapitulation of special problems of mineral recovery in the marine environment including such matters as the effect of water motion on mineral processing and of international law on investments. Glossaries of geological periods and technical terms, a short list of references, and an index complete the work.

  20. Investigating Minerals: Promoting Integrated Inquiry

    ERIC Educational Resources Information Center

    Thompson, Rudi; Carmack, Elizabeth

    2007-01-01

    "Mineral Detectives!" is one of eighteen lessons in the "Private Whys?" integrated science unit, which uses a guided inquiry investigation to teach students in grades three through five about the role of minerals in our lives. The University of North Texas developed "Private Whys?" with funding from the Copper…

  1. A Mineral Processing Field Course

    ERIC Educational Resources Information Center

    Carmody, Maurice

    2014-01-01

    This article describes a field course in Cornwall looking at mineral processing with the focus on the chemistry involved. The course was split into two parts. The first looked at tin mining based around Penzance. This involved visiting mines, hunting for mineral samples, carrying out a stream survey and visiting the Camborne School of Mines…

  2. Plant macro- and micronutrient minerals

    Technology Transfer Automated Retrieval System (TEKTRAN)

    All plants must obtain a number of inorganic mineral elements from their environment to ensure successful growth and development of both vegetative and reproductive tissues. A total of fourteen mineral nutrients are considered to be essential. Several other elements have been shown to have beneficia...

  3. Mineral Resources and the Environment.

    ERIC Educational Resources Information Center

    National Academy of Sciences, Washington, DC.

    This report presents the findings and recommendations of panels created by the Committee on Mineral Resources and the Environment (COMRATE) to study four topic areas of mineral resources and the environment. The topic areas studied by the panels were: technology, supply, the environment, and demand. Section I, the report of the technology panel,…

  4. Aluminum trichloride inhibits osteoblast mineralization via TGF-β1/Smad signaling pathway.

    PubMed

    Sun, Xudong; Cao, Zheng; Zhang, Qiuyue; Li, Miao; Han, Lulu; Li, Yanfei

    2016-01-25

    Osteoporosis is a major global public health problem. Aluminum (Al) exposure inhibits osteoblast mineralization and induces osteoporosis. However, the exact mechanism is not fully understood. The transforming growth factor β1 (TGF-β1)/Smad pathway is a major signaling cascade in regulating osteoblast mineralization. To investigate whether TGF-β1/Smad signaling pathway was involved in the Al-induced inhibition of osteoblast mineralization, osteoblasts were cultured and exposed to different concentrations of aluminum trichloride (AlCl3) (containing 0, 0.01, 0.02 and 0.04 mg/mL Al(3+)) for 24 h. We found that mineralized matrix nodules, mRNA expressions of alkaline phosphatase (ALP), type I collagen (Col I), TGF-β1, TGF-β type I receptor, TGF-β type II receptor and Smad4, protein expressions of TGF-β1 and p-Smad2/3, Smad2/3/4 trimeric complex were all decreased, whereas the mRNA expressions of Smad7 were increased in the AlCl3-treated groups compared with those in control. In conclusion, these results indicated that AlCl3 inhibited osteoblast mineralization via TGF-β1/Smad signaling pathway in rat osteoblasts. Our findings could provide novel insights into the mechanisms of action of AlCl3 in osteoporosis.

  5. Reliable Quantitative Mineral Abundances of the Martian Surface using THEMIS

    NASA Astrophysics Data System (ADS)

    Smith, R. J.; Huang, J.; Ryan, A. J.; Christensen, P. R.

    2013-12-01

    The following presents a proof of concept that given quality data, Thermal Emission Imaging System (THEMIS) data can be used to derive reliable quantitative mineral abundances of the Martian surface using a limited mineral library. The THEMIS instrument aboard the Mars Odyssey spacecraft is a multispectral thermal infrared imager with a spatial resolution of 100 m/pixel. The relatively high spatial resolution along with global coverage makes THEMIS datasets powerful tools for comprehensive fine scale petrologic analyses. However, the spectral resolution of THEMIS is limited to 8 surface sensitive bands between 6.8 and 14.0 μm with an average bandwidth of ~ 1 μm, which complicates atmosphere-surface separation and spectral analysis. This study utilizes the atmospheric correction methods of both Bandfield et al. [2004] and Ryan et al. [2013] joined with the iterative linear deconvolution technique pioneered by Huang et al. [in review] in order to derive fine-scale quantitative mineral abundances of the Martian surface. In general, it can be assumed that surface emissivity combines in a linear fashion in the thermal infrared (TIR) wavelengths such that the emitted energy is proportional to the areal percentage of the minerals present. TIR spectra are unmixed using a set of linear equations involving an endmember library of lab measured mineral spectra. The number of endmembers allowed in a spectral library are restricted to a quantity of n-1 (where n = the number of spectral bands of an instrument), preserving one band for blackbody. Spectral analysis of THEMIS data is thus allowed only seven endmembers. This study attempts to prove that this limitation does not prohibit the derivation of meaningful spectral analyses from THEMIS data. Our study selects THEMIS stamps from a region of Mars that is well characterized in the TIR by the higher spectral resolution, lower spatial resolution Thermal Emission Spectrometer (TES) instrument (143 bands at 10 cm-1 sampling and 3

  6. Ex situ aqueous mineral carbonation.

    PubMed

    Gerdemann, Stephen J; O'Connor, William K; Dahlin, David C; Penner, Larry R; Rush, Hank

    2007-04-01

    The U.S. Department of Energy's National Energy Technology Laboratory (NETL) located in Albany, OR (formerly the Albany Research Center) has studied ex situ mineral carbonation as a potential option for carbon dioxide sequestration. Studies focused on the reaction of Ca-, Fe-, and Mg-silicate minerals with gaseous CO2 to form geologically stable, naturally occurring solid carbonate minerals. The research included resource evaluation, kinetic studies, process development, and economic evaluation. An initial cost estimate of approximately $69/ton of CO2 sequestered was improved with process improvements to $54/ton. The scale of ex situ mineral carbonation operations, requiring 55 000 tons of mineral to carbonate, the daily CO2 emissions from a 1-GW, coal-fired power plant, may make such operations impractical.

  7. Mineral induced mechanochemical degradation: the imazaquin case.

    PubMed

    Nasser, Ahmed; Buchanovsky, Nadia; Gerstl, Zev; Mingelgrin, Uri

    2009-03-01

    The potential role of mechanochemical processes in enhancing degradation of imazaquin by soil components is demonstrated. The investigated components include montmorillonite saturated with Na(+), Ca(2+), Cu(2+)and Al(3+), Agsorb (a commercial clay mix), birnessite and hematite. The mechanical force applied was manual grinding of mixtures of imazaquin and the minerals, using mortar and pestle. The degradation rates of imazaquin in these mixtures were examined as a function of the following parameters: time of grinding, herbicide load (3.9, 8.9, 16.7 and 26.6 mg imazaquin per g mineral), temperature (10, 25, 40 and 70 degrees C), acidic/basic conditions, and dry or wet grinding. Dry grinding of imazaquin for 5 min with Al-montmorillonite or with hematite resulted in 56% and 71% degradation of the imazaquin, respectively. Wet grinding slightly reduced the degradation rate with hematite and entirely cancelled the enhancing effect of grinding with Al-montmorillonite. Wet grinding in the presence of the transition metals: Ni(2+), Cu(2+), Fe(3+) added as chlorides was carried out. Addition of Cu(2+) to Na-montmorillonite loaded with imazaquin was the most effective treatment in degrading imazaquin (more than 90% of the imazaquin degraded after 5 min of grinding). In this treatment, Cu-montmorillonite formation during the grinding process was confirmed by XRD and accordingly, grinding with Cu-montmorillonite gave similar degradation values. LC-MS analysis revealed that the mechanochemical transformation of imazaquin resulted in the formation of a dimer and several breakdown products. The reported results demonstrate once again that mechanochemical procedures offer a remediation avenue applicable to soils polluted with organic contaminants.

  8. Spatial Arrangment of Organic Compounds on a Model Mineral Surface: Implications for Soil Organic Matter Stabilization

    SciTech Connect

    Petridis, Loukas; Ambaye, Haile Arena; Jagadamma, Sindhu; Kilbey, S. Michael; Lokitz, Bradley S; Lauter, Valeria; Mayes, Melanie

    2014-01-01

    The complexity of the mineral organic carbon interface may influence the extent of stabilization of organic carbon compounds in soils, which is important for global climate futures. The nanoscale structure of a model interface was examined here by depositing films of organic carbon compounds of contrasting chemical character, hydrophilic glucose and amphiphilic stearic acid, onto a soil mineral analogue (Al2O3). Neutron reflectometry, a technique which provides depth-sensitive insight into the organization of the thin films, indicates that glucose molecules reside in a layer between Al2O3 and stearic acid, a result that was verified by water contact angle measurements. Molecular dynamics simulations reveal the thermodynamic driving force behind glucose partitioning on the mineral interface: The entropic penalty of confining the less mobile glucose on the mineral surface is lower than for stearic acid. The fundamental information obtained here helps rationalize how complex arrangements of organic carbon on soil mineral surfaces may arise

  9. 43 CFR 3816.1 - Mineral locations.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false Mineral locations. 3816.1 Section 3816.1..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LANDS AND MINERALS SUBJECT TO LOCATION Mineral Locations in Reclamation Withdrawals § 3816.1 Mineral locations. The Act of April 23, 1932 (47 Stat. 136;...

  10. 43 CFR 3816.1 - Mineral locations.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false Mineral locations. 3816.1 Section 3816.1..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LANDS AND MINERALS SUBJECT TO LOCATION Mineral Locations in Reclamation Withdrawals § 3816.1 Mineral locations. The Act of April 23, 1932 (47 Stat. 136;...

  11. 43 CFR 3816.1 - Mineral locations.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false Mineral locations. 3816.1 Section 3816.1..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LANDS AND MINERALS SUBJECT TO LOCATION Mineral Locations in Reclamation Withdrawals § 3816.1 Mineral locations. The Act of April 23, 1932 (47 Stat. 136;...

  12. 43 CFR 3815.1 - Mineral locations.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false Mineral locations. 3815.1 Section 3815.1..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LANDS AND MINERALS SUBJECT TO LOCATION Mineral Locations in Stock Driveway Withdrawals § 3815.1 Mineral locations. Under authority of the provisions of...

  13. 43 CFR 3815.1 - Mineral locations.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false Mineral locations. 3815.1 Section 3815.1..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LANDS AND MINERALS SUBJECT TO LOCATION Mineral Locations in Stock Driveway Withdrawals § 3815.1 Mineral locations. Under authority of the provisions of...

  14. 43 CFR 3816.1 - Mineral locations.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false Mineral locations. 3816.1 Section 3816.1..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LANDS AND MINERALS SUBJECT TO LOCATION Mineral Locations in Reclamation Withdrawals § 3816.1 Mineral locations. The Act of April 23, 1932 (47 Stat. 136;...

  15. 43 CFR 3815.1 - Mineral locations.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false Mineral locations. 3815.1 Section 3815.1..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LANDS AND MINERALS SUBJECT TO LOCATION Mineral Locations in Stock Driveway Withdrawals § 3815.1 Mineral locations. Under authority of the provisions of...

  16. 43 CFR 3815.1 - Mineral locations.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false Mineral locations. 3815.1 Section 3815.1..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LANDS AND MINERALS SUBJECT TO LOCATION Mineral Locations in Stock Driveway Withdrawals § 3815.1 Mineral locations. Under authority of the provisions of...

  17. 30 CFR 57.5070 - Miner training.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 1 2010-07-01 2010-07-01 false Miner training. 57.5070 Section 57.5070 Mineral... Agents, and Diesel Particulate Matter Diesel Particulate Matter-Underground Only § 57.5070 Miner training. (a) Mine operators must provide annual training to all miners at a mine covered by this part who...

  18. Mineral Commodity Profiles: Selenium

    USGS Publications Warehouse

    Butterman, W.C.; Brown, R.D.

    2004-01-01

    Overview -- Selenium, which is one of the chalcogen elements in group 16 (or 6A) of the periodic table, is a semiconductor that is chemically similar to sulfur for which it substitutes in many minerals and synthetic compounds. It is a byproduct of copper refining and, to a much lesser extent, lead refining. It is used in many applications, the major ones being a decolorizer for glass, a metallurgical additive to free-machining varieties of ferrous and nonferrous alloys, a constituent in cadmium sulfoselenide pigments, a photoreceptor in xerographic copiers, and a semiconductor in electrical rectifiers and photocells. Refined selenium amounting to more than 1,800 metric tons (t) was produced by 14 countries in 2000. Japan, Canada, the United States, and Belgium, which were the four largest producers, accounted for nearly 85 percent of world production. An estimated 250 t of the world total is secondary selenium, which is recovered from scrapped xerographic copier drums and selenium rectifiers; the selenium in nearly all other uses is dissipated (not recoverable as waste or scrap). The present selenium reserve bases for the United States and the world (including the United States), which are associated with copper deposits, are expected to be able to satisfy demand for selenium for several decades without difficulty.

  19. Universal ripper miner

    DOEpatents

    Morrell, Roger J.; Larson, David A.

    1991-01-01

    A universal ripper miner used to cut, collect and transfer material from an underground mine working face includes a cutter head that is vertically movable in an arcuate cutting cycle by means of drive members, such as hydraulically actuated pistons. The cutter head may support a circular cutter bit having a circular cutting edge that may be indexed to incrementally expose a fresh cutting edge. An automatic indexing system is disclosed wherein indexing occurs by means of a worm gear and indexing lever mechanism. The invention also contemplates a bi-directional bit holder enabling cutting to occur in both the upstroke and the downstroke cutting cycle. Another feature of the invention discloses multiple bits arranged in an in-line, radially staggered pattern, or a side-by-side pattern to increase the mining capacity in each cutting cycle. An on-board resharpening system is also disclosed for resharpening the cutting edge at the end of cutting stroke position. The aforementioned improvement features may be used either singly, or in any proposed combination with each other.

  20. Longwall mineral mining installation

    SciTech Connect

    Becker, K.; Beyer, H.

    1982-09-14

    A longwall mineral mining installation comprises a scraper-chain conveyor having a scraper assembly, a first straight conveyor portion extending along the longwall working, a second straight conveyor portion extending along a roadway positioned at one end of the longwall working, and a curved conveyor section connecting the two straight conveyor portions. A guide assembly is provided for guiding the scraper assembly around the curved conveyor section. A guide is fixed to the face side of the first straight conveyor portion, and a winning machine is reciprocable along the guide. A drive station is mounted on the goaf side of the first straight conveyor portion in the region of the curved conveyor section. A drive sprocket is rotatably mounted on the face side of the first straight conveyor portion in said region. The drive sprocket drives the winning machine via a drive chain. A drive shaft drivably connects the drive station and the drive sprocket. The drive station includes a drive motor whose axis of rotation is substantially parallel to the longitudinal axis of the first straight conveyor portion, and the guide is angled away from the first straight conveyor portion in said region.

  1. The roles of organic anion permeases in aluminium resistance and mineral nutrition.

    PubMed

    Delhaize, Emmanuel; Gruber, Benjamin D; Ryan, Peter R

    2007-05-25

    Soluble aluminium (Al(3+)) is the major constraint to plant growth on acid soils. Plants have evolved mechanisms to tolerate Al(3+) and one type of mechanism relies on the efflux of organic anions that protect roots by chelating the Al(3+). Al(3+) resistance genes of several species have now been isolated and found to encode membrane proteins that facilitate organic anion efflux from roots. These proteins belong to the Al(3+)-activated malate transporter (ALMT) and multi-drug and toxin extrusion (MATE) families. We review the roles of these proteins in Al(3+) resistance as well as their roles in other aspects of mineral nutrition.

  2. The role of secondary mineral precipitates on radionuclide sequestration at the Hanford Site

    SciTech Connect

    Um, Wooyong; Serne, R. Jeffrey; Yabusaki, Steven B.; Freedman, Vicky L.; Samson, Sherry D.; Nagy, Kathryn L.

    2004-06-27

    The effects of secondary mineral precipitates on radionuclide sequestration at the Hanford Site were investigated by reacting quartz and Hanford sediment (Warden Soil) with caustic solution of high ionic strength (2 M NaNO3), high pH (~13), high temperature (~90oC), and dissolved Al(0.01 M Al(NO3)3). Continuous Si dissolution and concomitant secondary mineral precipitation were the principal reactions observed. Nitrate-cancrinite was the dominant secondary precipitate on mineral surfaces after 3-10 days reaction time. The presence of dissolved Al in the simulated tank fluid was found to depress the net Si dissolved concentration. Based on batch equilibrium sorption results, secondary precipitates (cancrinite) at the primary mineral surfaces enhanced the sorption capacity of typical Hanford sediment for radionuclides of major concern at the Hanford Site such as 129I, 79Se, 99Tc, and 90Sr.

  3. Experimental dynamic metamorphism of mineral single crystals

    USGS Publications Warehouse

    Kirby, S.H.; Stern, L.A.

    1993-01-01

    This paper is a review of some of the rich and varied interactions between non-hydrostatic stress and phase transformations or mineral reactions, drawn mainly from results of experiments done on mineral single crystals in our laboratory or our co-authors. The state of stress and inelastic deformation can enter explicitly into the equilibrium phase relations and kinetics of mineral reactions. Alternatively, phase transformations can have prominent effects on theology and on the nature of inelastic deformation. Our examples represent five types of structural phase changes, each of which is distinguished by particular mechanical effects. In increasing structural complexity, these include: (1) displacive phase transformations involving no bond-breaking, which may produce anomalous brittle behavior. A primary example is the a-?? quartz transition which shows anomalously low fracture strength and tertiary creep behavior near the transition temperature; (2) martensitic-like transformations involving transformation strains dominated by shear deformation. Examples include the orthoenstatite ??? clinoenstatite and w u ??rtzite ??? sphalerite transformations; (3) coherent exsolution or precipitation of a mineral solute from a supersaturated solid-solution, with anisotropy of precipitation and creep rates produced under nonhydrostatic stress. Examples include exsolution of corundum from MgO ?? nAl2O3 spinels and Ca-clinopyroxene from orthopyroxene; (4) order-disorder transformations that are believed to cause anomalous plastic yield strengthening, such as MgO - nAl2O3 spinels; and (5) near-surface devolatilization of hydrous silicate single-crystals that produces a fundamental brittleness thought to be connected with dehydration at microcracks at temperatures well below nominal macroscopic dehydration temperatures. As none of these interactions between single-crystal phase transformations and non-hydrostatic stress is understood in detail, this paper serves as a challenge to

  4. [Study on the Influence of Mineralizer on the Preparation of Calcium Aluminates Based on Infrared Spectroscopy].

    PubMed

    Fan, Wei; Wang, Liang; Zheng, Huai-li; Chen, Wei; Tang, Xiao-min; Shang, Juan-fang; Qian, Li

    2015-05-01

    In this study, effect of mineralizer on the structure and spectraproperties of calcium aluminates formation was extensively studied. Medium or low-grade bauxite and calcium carbonate were used as raw material and mineralizer CaF2 as additive. Calcium aluminates can be obtained after mixing fully, calcination and grinding. The prepared calcium aluminates can be directly used for the production of polyaluminiumchloride (PAC), polymeric aluminum sulfate, sodium aluminate and some other water treatment agents. The calcium aluminates preparation technology was optimized by investigating the mass ratio of raw materials (bauxiteand calcium carbonate) and mineralizer CaF2 dosage. The structure and spectra properties of bauxite and calcium aluminates were characterized by Fourier transform infrared(FTIR) spectroscopy analysis and the mineralization mechanism of the mineralizer was studied. FTIR spectra indicated that the addition of mineralizer promoted the decomposition and transformation of the diaspore, gibbsite and kaolinite, the decomposition of calcium carbonate, and more adequately reaction between bauxite and calcium carbonate. In addition, not only Ca in calcium carbonate and Si in bauxite were more readily reacted, but also Si-O, Si-O-Al and Al-Si bonds in the bauxite were more fractured which contributed to the release of Al in bauxite, and therefore, the dissolution rate of Al2O3 could be improved. The dissolution rate of Al2O3 can be promoted effectively when the mineralizer CaF2 was added in a mass ratio amount of 3%. And the mineralizer CaF2 cannot be fully functioned, when its dosage was in a mass percent of 1. 5%. Low-grade bauxite was easier to sinter for the preparation of calcium aluminates comparing with the highgrade one. The optimum material ratio for the preparation of calcium aluminates calcium at 1 250 °C was the mass ratio between bauxite and calcium carbonate of 1 : 0. 6 and mineralizer CaF2 mass ratio percent of 3%.

  5. Economic drivers of mineral supply

    USGS Publications Warehouse

    Wagner, Lorie A.; Sullivan, Daniel E.; Sznopek, John L.

    2003-01-01

    The debate over the adequacy of future supplies of mineral resources continues in light of the growing use of mineral-based materials in the United States. According to the U.S. Geological Survey, the quantity of new materials utilized each year has dramatically increased from 161 million tons2 in 1900 to 3.2 billion tons in 2000. Of all the materials used during the 20th century in the United States, more than half were used in the last 25 years. With the Earth?s endowment of natural resources remaining constant, and increased demand for resources, economic theory states that as depletion approaches, prices rise. This study shows that many economic drivers (conditions that create an economic incentive for producers to act in a particular way) such as the impact of globalization, technological improvements, productivity increases, and efficient materials usage are at work simultaneously to impact minerals markets and supply. As a result of these economic drivers, the historical price trend of mineral prices3 in constant dollars has declined as demand has risen. When price is measured by the cost in human effort, the price trend also has been almost steadily downward. Although the United States economy continues its increasing mineral consumption trend, the supply of minerals has been able to keep pace. This study shows that in general supply has grown faster than demand, causing a declining trend in mineral prices.

  6. Thermal Conductivity Measurement of Synthesized Mantle Minerals

    NASA Astrophysics Data System (ADS)

    Asimow, P. D.; Luo, S.; Mosenfelder, J. L.; Liu, W.; Staneff, G. D.; Ahrens, T. J.; Chen, G.

    2002-12-01

    Direct thermal conductivity (k) measurement of mantle minerals is crucial to constrain the thermal profile of the Earth as well as geodynamic studies of the mantle (e.g., to determine the Rayleigh number). We have embarked on systematic multi-anvil syntheses of dense polycrystalline specimens of mantle phases of adequate size and zero porosity for precise thermal conductivity measurements by the 3ω method (\\textit{Cahill and Pohl, Phys. Rev. B, 1987}) under elevated temperatures (T). Coesite and stishovite (see \\textit{Luo et al., GRL, 2002}) as well as majorite and wadsleyite have been synthesized; ringwoodite and perovskite are scheduled. Preliminary thermal conductivity measurements at ambient pressure on coesite (120 - 300 K, 9.53 Wm-1K-1 at 300 K) are consistent with prior room temperature data (\\textit{Yukutake & Shimada, PEPI, 1978}), while our stishovite data at 300 K appear to be low (1.96 Wm-1K-1). Efforts are being made to extend the measurement to higher temperatures (e.g., above Debye temperature Θ D), thus allowing determination of k(T) relationship (say, k~ T-n); success will depend on the decomposition kinetics of these metastable phases. The pressure dependence of k of these synthesized samples can also be measured (\\textit{e.g., Osako et al., HPMPS-6, 2002; Xu et al., EOS, 2001}). Recent thermal conductivity measurement on LiF and Al2O_3 from shock wave loading (\\textit{Holland & Ahrens, 1998}) is consistent with the modeling on MgO and Al2O_3 (\\textit{Manga & Jeanloz, JGR, 1997}) with classical theories. Thus, k values at modest pressures and T (say, above Θ D) would allow extrapolation of k to appropriate mantle conditions.

  7. Mineral induction by immobilized phosphoproteins

    NASA Technical Reports Server (NTRS)

    Saito, T.; Arsenault, A. L.; Yamauchi, M.; Kuboki, Y.; Crenshaw, M. A.

    1997-01-01

    Dentin phosphoproteins are thought to have a primary role in the deposition of mineral on the collagen of dentin. In this study we determined the type of binding between collagen and phosphoproteins necessary for mineral formation onto collagen fibrils and whether the phosphate esters are required. Bovine dentin phosphophoryn or phosvitin from egg yolk were immobilized on reconstituted skin type I collagen fibrils by adsorption or by covalent cross-linking. In some samples the ester phosphate was removed from the covalently cross-linked phosphoproteins by treatment with acid phosphatase. All samples were incubated at 37 degrees C in metastable solutions that do not spontaneously precipitate. Reconstituted collagen fibrils alone did not induce mineral formation. The phosphoproteins adsorbed to the collagen fibrils desorbed when the mineralization medium was added, and mineral was not induced. The mineral induced by the cross-linked phosphoproteins was apatite, and the crystals were confined to the surface of the collagen fibrils. With decreasing medium saturation the time required for mineral induction increased. The interfacial tensions calculated for apatite formation by either phosphoprotein cross-linked to collagen were about the same as that for phosphatidic acid liposomes and hydroxyapatite. This similarity in values indicates that the nucleation potential of these highly phosphorylated surfaces is about the same. It is concluded that phosphoproteins must be irreversibly bound to collagen fibrils for the mineralization of the collagen network in solutions that do not spontaneously precipitate. The phosphate esters of phosphoproteins are required for mineral induction, and the carboxylate groups are not sufficient.

  8. Glycine Polymerization on Oxide Minerals

    NASA Astrophysics Data System (ADS)

    Kitadai, Norio; Oonishi, Hiroyuki; Umemoto, Koichiro; Usui, Tomohiro; Fukushi, Keisuke; Nakashima, Satoru

    2016-07-01

    It has long been suggested that mineral surfaces played an important role in peptide bond formation on the primitive Earth. However, it remains unclear which mineral species was key to the prebiotic processes. This is because great discrepancies exist among the reported catalytic efficiencies of minerals for amino acid polymerizations, owing to mutually different experimental conditions. This study examined polymerization of glycine (Gly) on nine oxide minerals (amorphous silica, quartz, α-alumina and γ-alumina, anatase, rutile, hematite, magnetite, and forsterite) using identical preparation, heating, and analytical procedures. Results showed that a rutile surface is the most effective site for Gly polymerization in terms of both amounts and lengths of Gly polymers synthesized. The catalytic efficiency decreased as rutile > anatase > γ-alumina > forsterite > α- alumina > magnetite > hematite > quartz > amorphous silica. Based on reported molecular-level information for adsorption of Gly on these minerals, polymerization activation was inferred to have arisen from deprotonation of the NH3 + group of adsorbed Gly to the nucleophilic NH2 group, and from withdrawal of electron density from the carboxyl carbon to the surface metal ions. The orientation of adsorbed Gly on minerals is also a factor influencing the Gly reactivity. The examination of Gly-mineral interactions under identical experimental conditions has enabled the direct comparison of various minerals' catalytic efficiencies and has made discussion of polymerization mechanisms and their relative influences possible Further systematic investigations using the approach reported herein (which are expected to be fruitful) combined with future microscopic surface analyses will elucidate the role of minerals in the process of abiotic peptide bond formation.

  9. Mineral Commodity Profiles -- Rubidium

    USGS Publications Warehouse

    Butterman, W.C.; Reese, R.G.

    2003-01-01

    Overview -- Rubidium is a soft, ductile, silvery-white metal that melts at 39.3 ?C. One of the alkali metals, it is positioned in group 1 (or IA) of the periodic table between potassium and cesium. Naturally occurring rubidium is slightly radioactive. Rubidium is an extremely reactive metal--it ignites spontaneously in the presence of air and decomposes water explosively, igniting the liberated hydrogen. Because of its reactivity, the metal and several of its compounds are hazardous materials, and must be stored and transported in isolation from possible reactants. Although rubidium is more abundant in the earth?s crust than copper, lead, or zinc, it forms no minerals of its own, and is, or has been, produced in small quantities as a byproduct of the processing of cesium and lithium ores taken from a few small deposits in Canada, Namibia, and Zambia. In the United States, the metal and its compounds are produced from imported raw materials by at least one company, the Cabot Corporation (Cabot, 2003). Rubidium is used interchangeably or together with cesium in many uses. Its principal application is in specialty glasses used in fiber optic telecommunication systems. Rubidium?s photoemissive properties have led to its use in night-vision devices, photoelectric cells, and photomultiplier tubes. It has several uses in medical science, such as in positron emission tomographic (PET) imaging, the treatment of epilepsy, and the ultracentrifugal separation of nucleic acids and viruses. A dozen or more other uses are known, which include use as a cocatalyst for several organic reactions and in frequency reference oscillators for telecommunications network synchronization. The market for rubidium is extremely small, amounting to 1 to 2 metric tons per year (t/yr) in the United States. World resources are vast compared with demand.

  10. Mineral Losses During Extreme Environmental Conditions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Advisory groups that make recommendations for mineral intakes continue to identify accurate determinations of sweat mineral losses during physical activity as a critical void in their deliberations. Although estimates of sweat mineral concentrations are available, they are highly variable. Practica...

  11. Mineral catalysis of a potentially prebiotic aldol condensation

    NASA Technical Reports Server (NTRS)

    De Graaf, R. M.; Visscher, J.; Xu, Y.; Arrhenius, G.; Schwartz, A. W.

    1998-01-01

    Minerals may have played a significant role in chemical evolution. In the course of investigating the chemistry of phosphonoacetaldehyde (PAL), an analogue of glycolaldehyde phosphate, we have observed a striking case of catalysis by the layered hydroxide mineral hydrotalcite ([Mg2Al(OH)6][Cl.nH2O]). In neutral or moderately basic aqueous solutions, PAL is unreactive even at a concentration of 0.1 M. In the presence of a large excess of NaOH (2 M), the compound undergoes aldol condensation to produce a dimer containing a C3-C4 double-bond. In dilute neutral solutions and in the presence of the mineral, however, condensation takes place rapidly, to produce a dimer which is almost exclusively the C2-C3 unsaturated product.

  12. Biologically enhanced mineral weathering: what does it look like, can we model it?

    NASA Astrophysics Data System (ADS)

    Schulz, M. S.; Lawrence, C. R.; Harden, J. W.; White, A. F.

    2011-12-01

    The interaction between plants and minerals in soils is hugely important and poorly understood as it relates to the fate of soil carbon. Plant roots, fungi and bacteria inhabit the mineral soil and work symbiotically to extract nutrients, generally through low molecular weight exudates (organic acids, extracelluar polysachrides (EPS), siderophores, etc.). Up to 60% of photosynthetic carbon is allocated below ground as roots and exudates, both being important carbon sources in soils. Some exudates accelerate mineral weathering. To test whether plant exudates are incorporated into poorly crystalline secondary mineral phases during precipitation, we are investigating the biologic-mineral interface. We sampled 5 marine terraces along a soil chronosequence (60 to 225 ka), near Santa Cruz, CA. The effects of the biologic interactions with mineral surfaces were characterized through the use of Scanning Electron Microscopy (SEM). Morphologically, mycorrhizal fungi were observed fully surrounding minerals, fungal hyphae were shown to tunnel into primary silicate minerals and we have observed direct hyphal attachment to mineral surfaces. Fungal tunneling was seen in all 5 soils by SEM. Additionally, specific surface area (using a nitrogen BET method) of primary minerals was measured to determine if the effects of mineral tunneling are quantifiable in older soils. Results suggest that fungal tunneling is more extensive in the primary minerals of older soils. We have also examined the influence of organic acids on primary mineral weathering during soil development using a geochemical reactive transport model (CrunchFlow). Addition of organic acids in our models of soil development at Santa Cruz result in decreased activity of Fe and Al in soil pore water, which subsequently alters the spatial extent of primary mineral weathering and kaolinite precipitation. Overall, our preliminary modeling results suggest biological processes may be an important but underrepresented aspect of

  13. Geology and regional setting of the Al Masane ancient mine area, southeastern Arabian Shield, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Conway, Clay M.

    1985-01-01

    Chemical characteristics of volcanic rocks at Al Masane and elsewhere, along with features such as zinc-copper-iron sulfide mineralization, rhyolite-basalt bimodality, and the quartz phenocryst-rich nature of the felsic rocks, are compatible with an unusually primitive tholeiitic island-arc origin for the strata and mineral deposits of the Habawnah mineral belt.

  14. Definitions of Health Terms: Minerals

    MedlinePlus

    ... Zinc is found in a wide variety of foods, and is found in most multivitamin/mineral supplements. Source : ... 20894 U.S. Department of Health and Human Services National Institutes of Health Page last updated ...

  15. GHGRP Minerals Sector Industrial Profile

    EPA Pesticide Factsheets

    EPA's Greenhouse Gas Reporting Program periodically produces detailed profiles of the various industries that report under the program. The profiles available for download below contain detailed analyses for the Minerals industry.

  16. Designing Clothing for Coal Miners

    ERIC Educational Resources Information Center

    Watkins, Susan M.

    1977-01-01

    Describes procedures taken by apparel design students, working in an industrial setting, in designing functional clothing for coal miners as part of the Armco Steel Corporation's Student Design Program. (TA)

  17. Shock-induced modifications of magnetic minerals from impact structures

    NASA Astrophysics Data System (ADS)

    Kontny, A. M.

    2013-05-01

    Meteorite impact structures are an important feature of most planetary surfaces. The effects of shock waves on the intrinsic magnetic properties of minerals and rocks are therefore essential for the understanding of magnetization processes related to impact events on Earth and other planetary bodies. Despite numerous observations on natural settings (Carporzen et al. 2005; Mang et al. 2012), and experimental studies (Louzada et al. 2010, 2011; Gattacecca et al 2007; Gilder et al. 2004; Mang et al. 2013) there remain uncertainties concerning the rock magnetic properties and the magnetization process related to natural impact structures on Earth. In general, the magnetic signature of terrestrial impact structures is a combined effect between disrupted main regional magnetic trends due to shock and / or thermal demagnetization and high-amplitude, short-wavelength magnetic anomalies in the centre of intermediate to large impact structures. Some large structures (>40 km) are reported to exhibit central high-amplitude anomalies but the dominant magnetic feature is a magnetic low (Pilkington and Grieve 1992). The latter observation is especially important for the giant non-magnetized impact basins on Mars. Therefore numerous studies focused on the understanding of the demagnetization processes during shock pressure (Gilder et al. 2004; Louzada et al. 2010, 2011; Rochette et al. 2003). Many investigations of terrestrial impact structures, however, demonstrated that a natural remanent magnetization (NRM), which is imprinted into terrestrial rocks by the Earth magnetic field, is the main cause of the observed magnetic anomalies. Magnetic signatures of impact structures on Earth are therefore thought to be a combination of three parameters: (1) composition and magnetic properties of the target rocks, (2) modification of rocks and magnetic minerals (fracturing and melting) due to impact-related p-T conditions, (3) acquisition of new natural remanent magnetization (TRM, SRM or

  18. Mineral and water nutrition.

    PubMed

    Beede, D K

    1991-07-01

    In providing minerals to dairy cattle it is important to distinguish between dietary requirements and feeding recommendations. The requirement is the absolute amount of an element needed to meet the animal's metabolic needs for maintenance, growth, pregnancy, and lactation divided by the coefficient of absorption; this is estimated by the factorial method. Actual estimates of requirements for lactating dairy cattle have been determined for Ca and P. The major difficulties in relying on the requirement estimate are that dry matter intake varies and the true absorption coefficient of the mixture of feeds in the ration generally is unknown. Therefore, feeding recommendations, based on feeding graded concentrations of an element, often offer more applicable information. With the exception of Ca and P, the current feeding recommendations for the other macrominerals, Mg, Na, K, Cl and S, have resulted from feeding trials. With certain environmental and physiologic situations the feeding recommendations may vary. For example, during heat stress the dietary K recommendation for the lactating cow should be higher than in cool weather because of increased sweating and decreased feed intake. Another example may be that the source of supplemental Mg may affect what dietary inclusion rate will yield optimal performance and should be recommended. An important consideration in dairy ration formulation in the future will address the interrelationships of the various macrominerals. There is accumulating evidence that shows that different concentrations of Na, Cl, and K may interrelate and affect lactational performance. Many times the naturally occurring concentrations of one or more of these elements may have to be associated with varying concentrations of the others in order to optimize animal performance and health. Much experimentation likely will examine these interrelationships in the future. Supplementation of trace elements in diets of dairy cattle is common practice. This

  19. 77 FR 56273 - Conflict Minerals

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-09-12

    ...We are adopting a new form and rule pursuant to Section 1502 of the Dodd-Frank Wall Street Reform and Consumer Protection Act relating to the use of conflict minerals. Section 1502 added Section 13(p) to the Securities Exchange Act of 1934, which requires the Commission to promulgate rules requiring issuers with conflict minerals that are necessary to the functionality or production of a......

  20. The Zapot pegmatite mineral county

    USGS Publications Warehouse

    Foord, E.E.; Soregaroli, A.E.; Gordon, H.M.

    1999-01-01

    The Zapot pegmatite is currently being mined for mineral specimens (chiefly amazonite, topaz and smoky quartz in miarolitic cavities), for gemstones (topaz and smoky quartz) and for decorative rock (amazonite). The deposit is owned and operated by Harvey Gordon Minerals of Reno, Nevada, and is the only amazonite-topaz mining operation in the state. Thousands of specimens from this operation have reached the collector market.

  1. Post-shock temperatures in minerals

    NASA Technical Reports Server (NTRS)

    Raikes, S. A.; Ahrens, T. J.

    1979-01-01

    An experimental technique for the measurement of post-shock temperatures in minerals is presented, and silicate post-shock temperature measurements are compared with theoretical calculations. The technique involves the use of infrared detectors to determine the brightness temperatures at 4.5 to 5.75 microns and 7 to 14 microns of samples shocked to between 5 and 30 GPa. Results obtained for aluminum 2024 and stainless steel 304, as well as for Bamble bronzite and synthetic crystal forsterite are found at low pressures to be considerably in excess of the temperatures predicted assuming a hydrodynamic rheology and isentropic release parallel to the Hugoniot. The results are shown to be in better agreement, however, with values calculated assuming elastoplastic behavior, and the post-shock temperatures of crystalline quartz are found to be in good agreement with those calculated by Mashimo et al. (1979) from release adiabat data.

  2. Aerated concrete with mineral dispersed reinforcing additives

    NASA Astrophysics Data System (ADS)

    Berdov, G. I.; Ilina, L. V.; Mukhina, I. N.; Rakov, M. A.

    2015-01-01

    To guarantee the production of aerated concrete with the lowest average density while ensuring the required strength it is necessary to use a silica component with a surface area of 250-300 m2 / kg. The article presents experimental data on grinding the silica component together with clinker to the optimum dispersion. This allows increasing the strength of non-autoclaved aerated concrete up to 33%. Furthermore, the addition to aerated concrete the mixture of dispersed reinforcing agents (wollastonite, diopside) and electrolytes with multiply charged cations and anions (1% Fe2 (SO4)3; Al2 (SO4)3) provides the growth of aerated concrete strength at 30 - 75%. As a cohesive the clinker, crushed together with silica and mineral supplements should be used. This increases the strength of aerated concrete at 65% in comparing with Portland cement.

  3. Hunting for eruption ages in accessory minerals

    NASA Astrophysics Data System (ADS)

    Vazquez, J. A.

    2012-12-01

    A primary goal in geochronology is to provide precise and accurate ages for tephras that serve as chronostratigraphic markers for constraining the timing and rates of volcanism, sedimentation, climate change, and catastrophic events in Earth history. Zircon remains the most versatile accessory mineral for dating silicic tephras due to its common preservation in distal pyroclastic deposits, as well as the robustness of its U-Pb and U-series systems even after host materials have been hydrothermally altered or weathered. Countless studies document that zircon may be complexly zoned in age due to inheritance, contamination, recycling of antecrysts, protracted crystallization in long-lived magma reservoirs, or any combination of these. Other accessory minerals such as allanite or chevkinite can retain similar records of protracted crystallization. If the goal is to date the durations of magmatic crystallization, differentiation, and/or magma residence, then these protracted chronologies within and between accessory minerals are a blessing. However, if the goal is to date the timing of eruption with high precision, i.e., absolute ages with millennial-scale uncertainties, then this age zoning is a curse. Observations from ion microprobe 238U-230Th dating of Pleistocene zircon and allanite provide insight into the record of near-eruption crystallization in accessory minerals and serve as a guide for high-precision whole-crystal dating. Although imprecise relative to conventional techniques, ion probe analysis allows high-spatial resolution 238U-230Th dating that can document multi-millennial age distributions at the crystal scale. Analysis of unpolished rims and continuous depth profiling of zircon from small and large volume eruptions (e.g., Coso, Mono Craters, Yellowstone) reveals that the final several micrometers of crystallization often yield ages that are indistinguishable from associated eruption ages from the 40Ar/39Ar or (U-Th)/He methods. Using this approach, we

  4. Mineral phases in the Comet Halley dust particles

    NASA Astrophysics Data System (ADS)

    Dikov, Iu. P.; Evlanov, E. N.; Zubkov, B. V.; Mukhin, L. M.; Nazarov, M. A.; Prilutskii, O. F.; Sagdeev, R. Z.; Fomenkova, M. N.

    1991-06-01

    Results are presented of the analyses of mass spectra of 517 grains collected from the Comet Halley dust, which were performed by the dust-impact mass spectrometers Puma 1,2 on board Vega. The results indicate the presence of H, C, N, O, Na, Mg, Al, Si, S, Ca, Cr, and Fe, distributed among silicates; oxides and hydroxides; carbonates and bicarbonates; sulfates and sulfides; and nitrates, cyanides, and rhodanides. These mineral components form various mixtures with organic matter.

  5. Andic soils : mineralogical effect onto organic matter dynamics, organic matter effect onto mineral dynamics, or both?

    NASA Astrophysics Data System (ADS)

    Basile-Doelsch, Isabelle; Amundson, Ronald; Balesdent, Jérome; Borschneck, Daniel; Bottero, Jean-Yves; Colin, Fabrice; de Junet, Alexis; Doelsch, Emmanuel; Legros, Samuel; Levard, Clément; Masion, Armand; Meunier, Jean-Dominique; Rose, Jérôme

    2014-05-01

    From a strictly mineralogical point of view, weathering of volcanic glass produces secondary phases that are short range ordered alumino-silicates (SRO-AlSi). These are imogolite tubes (2 to 3 nm of diameter) and allophane supposedly spheres (3.5 to 5 nm). Their local structure is composed of a curved gibbsite Al layer and Si tetrahedra in the vacancies (Q0). Proto-imogolites have the same local structure but are roof-shape nanoparticles likely representing the precursors of imogolite and allophanes (Levard et al. 2010). These structures and sizes give to the SRO-AlSi large specific surfaces and high reactivities. In some natural sites, imogolites and allophanes are formed in large quantities. Aging of these phases may lead to the formation of more stable minerals (halloysite, kaolinite and gibbsite) (Torn et al 1997). In natural environments, when the weathering of volcanic glass is associated with the establishment of vegetation, the soils formed are generally andosols. These soils are particularly rich in organic matter (OM), which is explained by the high ability of SRO-AlSi mineral phases to form bonds with organic compounds. In a first order "bulk" approach, it is considered that these bonds strongly stabilize the organic compounds as their mean age can reach more than 10 kyrs in some studied sites (Basile-Doelsch et al. 2005; Torn et al. 1997). However, the structure of the mineral phases present in andosols deserves more attention. Traditionally, the presence in the SRO-AlSi andosols was shown by selective dissolution approaches by oxalate and pyrophosphate. Using spectroscopic methods, mineralogical analysis of SRO-AlSi in andosols samples showed that these mineral phases were neither imogolites nor allophanes as originally supposed, but only less organized structures remained in a state of proto-imogolites (Basile-Doelsch al. 2005 ; Levard et al., 2012). The presence of OM would have an inhibitory effect on the formation of secondary mineral phases, by

  6. Mineral commodity profiles: nitrogen

    USGS Publications Warehouse

    Kramer, Deborah A.

    2004-01-01

    Overview -- Nitrogen (N) is an essential element of life and a part of all animal and plant proteins. As a part of the DNA and RNA molecules, nitrogen is an essential constituent of each individual's genetic blueprint. As an essential element in the chlorophyll molecule, nitrogen is vital to a plant's ability to photosynthesize. Some crop plants, such as alfalfa, peas, peanuts, and soybeans, can convert atmospheric nitrogen into a usable form by a process referred to as 'fixation.' Most of the nitrogen that is available for crop production, however, comes from decomposing animal and plant waste or from commercially produced fertilizers. Commercial fertilizers contain nitrogen in the form of ammonium and/or nitrate or in a form that is quickly converted to the ammonium or nitrate form once the fertilizer is applied to the soil. Ammonia is generally the source of nitrogen in fertilizers. Anhydrous ammonia is commercially produced by reacting nitrogen with hydrogen under high temperatures and pressures. The source of nitrogen is the atmosphere, which is almost 80 percent nitrogen. Hydrogen is derived from a variety of raw materials, which include water, and crude oil, coal, and natural gas hydrocarbons. Nitrogen-based fertilizers are produced from ammonia feedstocks through a variety of chemical processes. Small quantities of nitrates are produced from mineral resources principally in Chile. In 2002, anhydrous ammonia and other nitrogen materials were produced in more than 70 countries. Global ammonia production was 108 million metric tons (Mt) of contained nitrogen. With 28 percent of this total, China was the largest producer of ammonia. Asia contributed 46 percent of total world ammonia production, and countries of the former U.S.S.R. represented 13 percent. North America also produced 13 percent of the total; Western Europe, 9 percent; the Middle East, 7 percent; Central America and South America, 5 percent; Eastern Europe, 3 percent; and Africa and Oceania

  7. The phosphate mineral arrojadite-(KFe) and its spectroscopic characterization

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; Xi, Yunfei; Scholz, Ricardo; Horta, Laura Frota Campos

    2013-05-01

    The arrojadite-(KFe) mineral has been analyzed using a combination of scanning electron microscopy and a combination of Raman and infrared spectroscopy. The origin of the mineral is Rapid Creek sedimentary phosphatic iron formation, northern Yukon. The formula of the mineral was determined as KNaCaNa(FeMgMn)Al(PO)10.85(POOH)(OH)2. The complexity of the mineral formula is reflected in the spectroscopy. Raman bands at 975, 991 and 1005 cm-1 with shoulder bands at 951 and 1024 cm-1 are assigned to the PO43- ν1 symmetric stretching modes. The Raman bands at 1024, 1066, 1092, 1123, 1148 and 1187 cm-1 are assigned to the PO43- ν3 antisymmetric stretching modes. A series of Raman bands observed at 540, 548, 557, 583, 604, 615 and 638 cm-1 are attributed to the ν4 out of plane bending modes of the PO4 and H2PO4 units. The ν2 PO4 and H2PO4 bending modes are observed at 403, 424, 449, 463, 479 and 513 cm-1. Hydroxyl and water stretching bands are readily observed. Vibrational spectroscopy enables new information about the complex phosphate mineral arrojadite-(KFe) to be obtained.

  8. [Mineral water as a cure].

    PubMed

    Nocco, Priska Binz

    2008-01-01

    The treatment of diseases with mineral spring water belongs to the oldest medical therapies. The "remedy" mineral water is therefore of importance also within the pharmacy. The present pharmacy historical work examines the impact of the use of mineral waters, as well as of their dried components, as therapeutic agents in the 19th and early 20th centuries, i.e. from approx. 1810 to 1930, as well as the contributions given by pharmacists in the development and analysis of mineral water springs. Beside these aspects, the aim here is also to describe the role played by pharmacists in the production of artificial mineral water as well as in the sale and wholesale of natural and artificial mineral water. In the first part of this work the situation in Switzerland and its surrounding countries, such as Germany, France, Italy and Austria, is discussed. The second part contains a case-study of the particular situation in the Canton Tessin. It is known from the scientific literature published at that time that information on mineral water was frequently reported. Starting from the beginning of the 19th century the number of such publications increased tremendously. The major part of them were publications in scientific journals or contributions to medical and pharmaceutical manuals and reference books. In particular the spa-related literature, such as spa-guides, was of growing interest to a broad public. The inclusion of monographs into the Swiss, the Cantonal as well the foreign pharmacopoeias granted a legal frame for the mineral waters and their dried components. These works are of major importance from a pharmacy historical standpoint and represent a unique proof of historical evidence of the old medicinal drug heritage. The most frequently used therapies based on mineral waters were drinking and bath cures. Several diseases, particularly those of a chronic character, were treated with mineral waters. The positive influence of these cures on the recovery of the patients

  9. Microbial mineral colonization across a subsurface redox transition zone

    SciTech Connect

    Converse, Brandon J.; McKinley, James P.; Resch, Charles T.; Roden, Eric E.

    2015-08-28

    Here our study employed 16S rRNA gene amplicon pyrosequencing to examine the hypothesis that chemolithotrophic Fe(II)-oxidizing bacteria (FeOB) would preferentially colonize the Fe(II)-bearing mineral biotite compared to quartz sand when the minerals were incubated in situ within a subsurface redox transition zone (RTZ) at the Hanford 300 Area site in Richland, WA, USA. The work was motivated by the recently documented presence of neutral-pH chemolithotrophic FeOB capable of oxidizing structural Fe(II) in primary silicate and secondary phyllosilicate minerals in 300 Area sediments and groundwater (Benzine et al., 2013). Sterilized portions of sand+biotite or sand alone were incubated in situ for 5 months within a multilevel sampling (MLS) apparatus that spanned a ca. 2-m interval across the RTZ in two separate groundwater wells. Parallel MLS measurements of aqueous geochemical species were performed prior to deployment of the minerals. Contrary to expectations, the 16S rRNA gene libraries showed no significant difference in microbial communities that colonized the sand+biotite vs. sand-only deployments. Both mineral-associated and groundwater communities were dominated by heterotrophic taxa, with organisms from the Pseudomonadaceae accounting for up to 70% of all reads from the colonized minerals. These results are consistent with previous results indicating the capacity for heterotrophic metabolism (including anaerobic metabolism below the RTZ) as well as the predominance of heterotrophic taxa within 300 Area sediments and groundwater. Although heterotrophic organisms clearly dominated the colonized minerals, several putative lithotrophic (NH4+, H2, Fe(II), and HS- oxidizing) taxa were detected in significant abundance above and within the RTZ. Such organisms may play a role in the coupling of anaerobic microbial metabolism to oxidative pathways with attendant impacts on elemental cycling and redox-sensitive contaminant

  10. Microbial mineral colonization across a subsurface redox transition zone

    DOE PAGES

    Converse, Brandon J.; McKinley, James P.; Resch, Charles T.; ...

    2015-08-28

    Here our study employed 16S rRNA gene amplicon pyrosequencing to examine the hypothesis that chemolithotrophic Fe(II)-oxidizing bacteria (FeOB) would preferentially colonize the Fe(II)-bearing mineral biotite compared to quartz sand when the minerals were incubated in situ within a subsurface redox transition zone (RTZ) at the Hanford 300 Area site in Richland, WA, USA. The work was motivated by the recently documented presence of neutral-pH chemolithotrophic FeOB capable of oxidizing structural Fe(II) in primary silicate and secondary phyllosilicate minerals in 300 Area sediments and groundwater (Benzine et al., 2013). Sterilized portions of sand+biotite or sand alone were incubated in situ formore » 5 months within a multilevel sampling (MLS) apparatus that spanned a ca. 2-m interval across the RTZ in two separate groundwater wells. Parallel MLS measurements of aqueous geochemical species were performed prior to deployment of the minerals. Contrary to expectations, the 16S rRNA gene libraries showed no significant difference in microbial communities that colonized the sand+biotite vs. sand-only deployments. Both mineral-associated and groundwater communities were dominated by heterotrophic taxa, with organisms from the Pseudomonadaceae accounting for up to 70% of all reads from the colonized minerals. These results are consistent with previous results indicating the capacity for heterotrophic metabolism (including anaerobic metabolism below the RTZ) as well as the predominance of heterotrophic taxa within 300 Area sediments and groundwater. Although heterotrophic organisms clearly dominated the colonized minerals, several putative lithotrophic (NH4+, H2, Fe(II), and HS- oxidizing) taxa were detected in significant abundance above and within the RTZ. Such organisms may play a role in the coupling of anaerobic microbial metabolism to oxidative pathways with attendant impacts on elemental cycling and redox-sensitive contaminant behavior in the vicinity of the RTZ.« less

  11. Microbial mineral colonization across a subsurface redox transition zone

    PubMed Central

    Converse, Brandon J.; McKinley, James P.; Resch, Charles T.; Roden, Eric E.

    2015-01-01

    This study employed 16S rRNA gene amplicon pyrosequencing to examine the hypothesis that chemolithotrophic Fe(II)-oxidizing bacteria (FeOB) would preferentially colonize the Fe(II)-bearing mineral biotite compared to quartz sand when the minerals were incubated in situ within a subsurface redox transition zone (RTZ) at the Hanford 300 Area site in Richland, WA, USA. The work was motivated by the recently documented presence of neutral-pH chemolithotrophic FeOB capable of oxidizing structural Fe(II) in primary silicate and secondary phyllosilicate minerals in 300 Area sediments and groundwater (Benzine et al., 2013). Sterilized portions of sand+biotite or sand alone were incubated in situ for 5 months within a multilevel sampling (MLS) apparatus that spanned a ca. 2-m interval across the RTZ in two separate groundwater wells. Parallel MLS measurements of aqueous geochemical species were performed prior to deployment of the minerals. Contrary to expectations, the 16S rRNA gene libraries showed no significant difference in microbial communities that colonized the sand+biotite vs. sand-only deployments. Both mineral-associated and groundwater communities were dominated by heterotrophic taxa, with organisms from the Pseudomonadaceae accounting for up to 70% of all reads from the colonized minerals. These results are consistent with previous results indicating the capacity for heterotrophic metabolism (including anaerobic metabolism below the RTZ) as well as the predominance of heterotrophic taxa within 300 Area sediments and groundwater. Although heterotrophic organisms clearly dominated the colonized minerals, several putative lithotrophic (NH4+, H2, Fe(II), and HS- oxidizing) taxa were detected in significant abundance above and within the RTZ. Such organisms may play a role in the coupling of anaerobic microbial metabolism to oxidative pathways with attendant impacts on elemental cycling and redox-sensitive contaminant behavior in the vicinity of the RTZ. PMID

  12. Mineral-resource data bases

    USGS Publications Warehouse

    ,

    1997-01-01

    Data bases are essential for modern scientific research. The new and exciting work being done in the Mineral Resource Program in the U.S. Geological Survey (USGS) usually begins with the question, "Where are the known deposits?" A mineral-resource data base containing this type of information and more can be useful not just to USGS scientists, but to anyone who needs such data. Users of the data bases from outside the USGS include mining and exploration companies, environmental groups, academia, other Federal Agencies, and the general public. At present, the USGS has two large mineral-resource data bases, MRDS (Mineral Resource Data System) and MAS (Minerals Availability System). MRDS was built and is mamtained by the USGS, and MAS was built and maintained by the Bureau of Mines. In 1996, after the Bureau was abolished, MAS was transferred to the USGS. The two data bases were compiled for different purposes and contain very different mformation. For instance, MAS contains information on costs, details of mining methods, and feasibility studies. MRDS has mineralogical and geologic data that are not contained in MAS. Because they are both mineral-resource data bases, however, they contain some information in common, such as location, name(s) of sites, and commodities present. Both data bases are international in scope, and both are quite large. MRDS contains over 110,000 records, while MAS has over 220,000. One reason that MAS has more records is that it contains information on smelters, mill sites, and fossil fuel sites, as well as mineral- resource sites. The USGS is working to combine the information in both data bases. This is a large undertaking that will require some years to complete. In the interim, information from both data bases will still be available

  13. Biomineralization: mineral formation by organisms

    NASA Astrophysics Data System (ADS)

    Addadi, Lia; Weiner, Steve

    2014-09-01

    Organisms form many different types of minerals, with diverse shapes and sizes. These minerals fulfill a variety of functions. Inspired by the late H A Lowenstam, Steve Weiner and Lia Addadi have addressed many questions that relate to the mechanisms by which biological organisms produce these mineral phases and how their structures relate to their functions. Addadi and Weiner have explored the manner in which macromolecules extracted from mineralized tissues can interact with some crystal planes and not others, how these macromolecules can be occluded inside the forming crystals residing preferentially on specific crystal planes, and how they can induce one polymorph of calcium carbonate and not another to nucleate. Addadi and Weiner have also identified a novel strategy used by the sea urchin to form its smooth and convoluted mineralized skeletal elements. The strategy involves the initial production by cells of a highly disordered mineral precursor phase in vesicles, and then the export of this so-called amorphous phase to the site of skeletal formation, where it crystallizes. This strategy is now known to be used by many different invertebrate phyla, as well as by vertebrates to build bones and teeth. One of the major current research aims of the Weiner--Addadi group is to understand the biomineralization pathways whereby ions are extracted from the environment, are transported and deposited inside cells within vesicles, how these disordered phases are then transferred to the site of skeletal formation, and finally how the so-called amorphous phase crystallizes. Biology has clearly evolved unique strategies for forming crystalline minerals. Despite more than 300 years of research in this field, many challenging questions still remain unanswered.

  14. The maximum water storage capacities in nominally anhydrous minerals in the mantle transition zone and lower mantle

    NASA Astrophysics Data System (ADS)

    Inoue, T.; Yurimoto, H.

    2012-12-01

    Water is the most important volatile component in the Earth, and affects the physicochemical properties of mantle minerals, e.g. density, elastic property, electrical conductivity, thermal conductivity, rheological property, melting temperature, melt composition, element partitioning, etc. So many high pressure experiments have been conducted so far to determine the effect of water on mantle minerals. To clarify the maximum water storage capacity in nominally anhydrous mantle minerals in the mantle transition zone and lower mantle is an important issue to discuss the possibility of the existence of water reservoir in the Earth mantle. So we have been clarifying the maximum water storage capacity in mantle minerals using MA-8 type (KAWAI-type) high pressure apparatus and SIMS (secondary ion mass spectroscopy). Upper mantle mineral, olivine can contain ~0.9 wt% H2O in the condition just above 410 km discontinuity in maximum (e.g. Chen et al., 2002; Smyth et al., 2006). On the other hand, mantle transition zone mineral, wadsleyite and ringwoodite can contain significant amount (about 2-3 wt.%) of H2O (e.g. Inoue et al., 1995, 1998, 2010; Kawamoto et al., 1996; Ohtani et al., 2000). But the lower mantle mineral, perovskite can not contain significant amount of H2O, less than ~0.1 wt% (e.g. Murakami et al., 2002; Inoue et al., 2010). In addition, garnet and stishovite also can not contain significant amount of H2O (e.g. Katayama et al., 2003; Mookherjee and Karato, 2010; Litasov et al., 2007). On the other hand, the water storage capacities of mantle minerals are supposed to be significantly coupled with Al by a substitution with Mg2+, Si4+ or Mg2+ + Si4+, because Al3+ is the trivalent cation, and H+ is the monovalent cation. To clarify the degree of the substitution, the water contents and the chemical compositions of Al-bearing minerals in the mantle transition zone and the lower mantle were also determined in the Al-bearing systems with H2O. We will introduce the

  15. Melting phase relations of a mica-clinopyroxenite from the Milk River area, southern Alberta, Canada

    NASA Astrophysics Data System (ADS)

    Funk, Sean P.; Luth, Robert W.

    2013-08-01

    Melting experiments were conducted on a mica-clinopyroxenite xenolith brought up in a minette dyke in southern Alberta, Canada, near Milk River. Both the minettes and mica-clinopyroxenite xenoliths were studied by Buhlmann et al. (Can J Earth Sci 37:1629-1650, 2000), who hypothesized that the minettes formed by partial melting of a mantle source containing clinopyroxene + phlogopite ± olivine, at pressures ≥1.7 GPa. In liquidus experiments performed on the most primitive minette in our previous study (Funk and Luth in Contrib Mineral Petrol 164:999-1009, 2012), we found a multiple saturation point where olivine and orthopyroxene coexisted with liquid at 1.77 GPa and 1,350 °C. We argued that the minette originally formed by partial melting of clinopyroxene + phlogopite, but had re-equilibrated with a harzburgite during ascent. In the current study, we wanted to test both the source region hypothesis of Buhlmann et al. and our re-equilibration hypothesis by studying the near-solidus phase equilibria of a mica + clinopyroxene assemblage. We found the solidus for our xenolith has a steep slope in P-T space and lies at temperatures above those of a normal cratonic geotherm, implying that this mica-clinopyroxenite is stable in the cratonic mantle. Melting could occur at greater depths, where the solidus is extrapolated to cross the geotherm or must be induced either by raising the temperatures of the surrounding rocks or by introducing hydrous fluids into the source. Our melts are in equilibrium with clinopyroxene and olivine. The compositions of the liquids derived from melting this xenolith are similar to madupitic lamproites from the Leucite Hills, Wyoming, studied by Carmichael (Contrib Mineral Petrol 15:24-66, 1967) and Barton and Hamilton (Contrib Mineral Petrol 66:41-49, 1978; Contrib Mineral Petrol 69:133-142, 1979). Barton and Hamilton (Contrib Mineral Petrol 69:133-142, 1979) proposed that the madupitic lamproites may have come from a source containing mica

  16. What Is ALS?

    MedlinePlus

    ... Javits, actor David Niven, “Sesame Street” creator Jon Stone, boxing champion Ezzard Charles, NBA Hall of Fame ... Help for People with ALS and Caregivers Read stories from families living with ALS Forms of ALS ...

  17. 43 CFR 3861.3 - Mineral surveyors.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false Mineral surveyors. 3861.3 Section 3861.3..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) MINERAL PATENT APPLICATIONS Surveys and Plats § 3861.3 Mineral surveyors....

  18. 21 CFR 573.680 - Mineral oil.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 6 2012-04-01 2012-04-01 false Mineral oil. 573.680 Section 573.680 Food and... Listing § 573.680 Mineral oil. Mineral oil may be safely used in animal feed, subject to the provisions of this section. (a) Mineral oil, for the purpose of this section, is that complying with the...

  19. 43 CFR 8.5 - Mineral rights.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false Mineral rights. 8.5 Section 8.5 Public... INTERIOR AND OF THE ARMY RELATIVE TO RESERVOIR PROJECT LANDS § 8.5 Mineral rights. Mineral, oil and gas..., but mineral rights not acquired will be subordinated to the Government's right to regulate...

  20. 21 CFR 573.680 - Mineral oil.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Mineral oil. 573.680 Section 573.680 Food and... Listing § 573.680 Mineral oil. Mineral oil may be safely used in animal feed, subject to the provisions of this section. (a) Mineral oil, for the purpose of this section, is that complying with the...

  1. 43 CFR 8.5 - Mineral rights.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 1 2013-10-01 2013-10-01 false Mineral rights. 8.5 Section 8.5 Public... INTERIOR AND OF THE ARMY RELATIVE TO RESERVOIR PROJECT LANDS § 8.5 Mineral rights. Mineral, oil and gas..., but mineral rights not acquired will be subordinated to the Government's right to regulate...

  2. 21 CFR 573.680 - Mineral oil.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Mineral oil. 573.680 Section 573.680 Food and... Listing § 573.680 Mineral oil. Mineral oil may be safely used in animal feed, subject to the provisions of this section. (a) Mineral oil, for the purpose of this section, is that complying with the...

  3. 43 CFR 8.5 - Mineral rights.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 1 2011-10-01 2011-10-01 false Mineral rights. 8.5 Section 8.5 Public... INTERIOR AND OF THE ARMY RELATIVE TO RESERVOIR PROJECT LANDS § 8.5 Mineral rights. Mineral, oil and gas..., but mineral rights not acquired will be subordinated to the Government's right to regulate...

  4. 21 CFR 573.680 - Mineral oil.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Mineral oil. 573.680 Section 573.680 Food and... Listing § 573.680 Mineral oil. Mineral oil may be safely used in animal feed, subject to the provisions of this section. (a) Mineral oil, for the purpose of this section, is that complying with the...

  5. 43 CFR 8.5 - Mineral rights.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 1 2012-10-01 2011-10-01 true Mineral rights. 8.5 Section 8.5 Public... INTERIOR AND OF THE ARMY RELATIVE TO RESERVOIR PROJECT LANDS § 8.5 Mineral rights. Mineral, oil and gas..., but mineral rights not acquired will be subordinated to the Government's right to regulate...

  6. 43 CFR 3861.3 - Mineral surveyors.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false Mineral surveyors. 3861.3 Section 3861.3..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) MINERAL PATENT APPLICATIONS Surveys and Plats § 3861.3 Mineral surveyors....

  7. 43 CFR 3861.3 - Mineral surveyors.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false Mineral surveyors. 3861.3 Section 3861.3..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) MINERAL PATENT APPLICATIONS Surveys and Plats § 3861.3 Mineral surveyors....

  8. 43 CFR 3861.3 - Mineral surveyors.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false Mineral surveyors. 3861.3 Section 3861.3..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) MINERAL PATENT APPLICATIONS Surveys and Plats § 3861.3 Mineral surveyors....

  9. 21 CFR 573.680 - Mineral oil.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 6 2014-04-01 2014-04-01 false Mineral oil. 573.680 Section 573.680 Food and... Listing § 573.680 Mineral oil. Mineral oil may be safely used in animal feed, subject to the provisions of this section. (a) Mineral oil, for the purpose of this section, is that complying with the...

  10. 43 CFR 3830.10 - Locatable minerals.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false Locatable minerals. 3830.10 Section 3830..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LOCATING, RECORDING, AND MAINTAINING MINING CLAIMS OR SITES; GENERAL PROVISIONS Mining Law Minerals § 3830.10 Locatable minerals....

  11. 43 CFR 8.5 - Mineral rights.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 1 2014-10-01 2014-10-01 false Mineral rights. 8.5 Section 8.5 Public... INTERIOR AND OF THE ARMY RELATIVE TO RESERVOIR PROJECT LANDS § 8.5 Mineral rights. Mineral, oil and gas..., but mineral rights not acquired will be subordinated to the Government's right to regulate...

  12. 43 CFR 3830.10 - Locatable minerals.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false Locatable minerals. 3830.10 Section 3830..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LOCATING, RECORDING, AND MAINTAINING MINING CLAIMS OR SITES; GENERAL PROVISIONS Mining Law Minerals § 3830.10 Locatable minerals....

  13. 43 CFR 3830.10 - Locatable minerals.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false Locatable minerals. 3830.10 Section 3830..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LOCATING, RECORDING, AND MAINTAINING MINING CLAIMS OR SITES; GENERAL PROVISIONS Mining Law Minerals § 3830.10 Locatable minerals....

  14. 43 CFR 3830.10 - Locatable minerals.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false Locatable minerals. 3830.10 Section 3830..., DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) LOCATING, RECORDING, AND MAINTAINING MINING CLAIMS OR SITES; GENERAL PROVISIONS Mining Law Minerals § 3830.10 Locatable minerals....

  15. 1996 annual report on Alaska's mineral resources

    USGS Publications Warehouse

    Schneider, Jill L.

    1997-01-01

    This is the fifteenth annual report that has been prepared in response to the Alaska National Interest Lands Conservation Act. Current Alaskan mineral projects and events that occurred during 1995 are summarized. For the purpose of this document, the term 'minerals' encompasses both energy resources (oil and gas, coal and peat, uranium, and geothermal) and nonfuel-mineral resources (metallic and industrial minerals).

  16. Portable Radiometer Identifies Minerals in the Field

    NASA Technical Reports Server (NTRS)

    Goetz, A. F. H.; Machida, R. A.

    1982-01-01

    Hand-held optical instrument aids in identifying minerals in field. Can be used in exploration for minerals on foot or by aircraft. The radiometer is especially suitable for identifying clay and carbonate minerals. Radiometer measures reflectances of mineral at two wavelengths, computes ratio of reflectances, and displays ratio to user.

  17. Considerations on the Mo mineralization from the Mraconia perimeter

    NASA Astrophysics Data System (ADS)

    Anason, M. A.; Marincea, S. T.; Dumitras, D. G.; Iancu, A. M.

    2012-04-01

    The molybdenum contents recorded in the prelaramic magmatite from the area, using emission spectroscopy, do not exceed in general the values of 3 ppm (Vlad et al., 1984, Vieru et al., 1990) placing them around the average of 2.5 ppm gave by Sandell si Goldich 1943 (fide Rankama, Sahama, 1968) for " salicylic magmatite". Two samples of porphyry granodiorites collected from the Mraconia Valley 7th gallery make an exception from the values just mentioned. The Mo contents of this two are 3.5 ppm and 42 ppm respectively (Vlad et al., 1984). Clearly these contents are insignificants in the crystalline limstones case because of the calcophile extreme of the molybdenite mineral. The preveous data argues, in a satisfactory way, the exclusive presence of the molybdenite mineral in the "quartz und molibdenum" formation. Apart from the field work, geological research involves and laboratory studies of the collected material and its analysis by applying various methods of analysis: physical, chemical or using a combination of these. The rock samples with molybdenum mineralization were collected from different parts of the Mraconia Valley. They have been observed both, macroscopic, directly in the field, and microscopic using a Carl Zeiss Jenapol petro-graphic microscope. For the determination of Mo contents was used the spectrographic emission method on 16 samples. The molybdenite mineral (MoS2) appears as being characteristic to the hypo-mesothermal phases in the hydrothermal formation called "quartz und molybdenum", located, with maximum frequency at the contact of the granite bodies and quarto-chlorite schist, belongs to the Corbu crystalline, but sometimes appears as impregnations in the granodiorites and metasomatites mass. The macroscopic observations have revealed that the molybdenite mineral dos not form relationship with other sulphides, except pyrite, which prevents the crystallizations compared with other minerals. The presence in some associations is due to the late

  18. Recommended nomenclature for zeolite minerals: report of the subcommittee on zeolites of the International Mineralogical Association, Commission on new Minerals and Mineral names

    USGS Publications Warehouse

    Coombs, D.S.; Alberti, A.; Armbruster, T.; Artioli, G.; Colella, C.; Galli, E.; Grice, Joel D.; Liebau, F.; Mandarino, J.A.; Minato, H.; Nickel, E.H.; Passaglia, E.; Peacor, D.R.; Quartieri, S.; Rinaldi, R.; Ross, M.; Sheppard, R.A.; Tillmanns, E.; Vezzalini, G.

    1997-01-01

    This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association, Commission on New Minerals and Mineral Names. In a working definition of a zeolite mineral used for this review, structures containing an interrupted framework of tetrahedra are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is allowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundant in atomic proportions. To name these, the appropriate chemicalsymbol is attached by a hyphen to the series name as a suffix, except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely on the ratio Si:Al except for heulandite (Si:Al < 4.0) and clinoptilolite (Si:Al ??? 4.0). Dehydration, partial hydration, and overhydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of a zeolite. newly recognized species in compositional series are as follows: brewsterite-Sr, -Ba, chabazite-Ca, -Na, -K, clinoptilolite-K, -Na, -Ca, dachiardite-Ca, -Na, erionite-Na, erionite-Na, -K, -Ca, faujasite-Na, -Ca, -Mg, ferrierite-Mg, -K, -Na, gmelinite-Na, -Ca, -K, heulandite-Ca, -Na, -K, -Sr, levyne-Ca, -Na, paulingite-K, -Ca, phillipsite-Na, -Ca, -K, and stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data, IZA structure-type symbols, space-group symmetry, unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species

  19. Recommended nomenclature for zeolite minerals: Report of the Subcommittee on Zeolites of the International Mineralogical Association, Commission on New Minerals and Mineral Names

    USGS Publications Warehouse

    Coombs, D.S.; Alberti, A.; Armbruster, T.; Artioli, G.; Colella, C.; Galli, E.; Grice, Joel D.; Liebau, F.; Mandarino, J.A.; Minato, H.; Nickel, E.H.; Passaglia, E.; Peacor, D.R.; Quartieri, S.; Rinaldi, R.; Ross, M.; Sheppard, R.A.; Tillmanns, E.; Vezzalini, G.

    1998-01-01

    This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association Commission on New Minerals and Mineral Names. In a working definition of a zeolite mineral used for this review, structures containing an interrupted containing an interrupted framework of tetrahedra are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is alloowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundant in atomic proportions. To name these, the appropriate chemical symbol is attached by a hyphen to the series name as a suffix, except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely in Si:Al ratio except for heulandite (Si:Al < 4.0) and clinoptilolite (Si:Al ??? 4.0). Dehydration, partial hydration and over-hydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of zeolite. Newly recognized species in compositional series are as follows: brewsterite-Sr, -Ba; chabazite-Ca, -Na, -K; clinoptilolite-K, -Na, -Ca; dechiardite-Ca, -Na; erionite-Na, -K, -Ca,; faujasite-Na, -Ca, -Mg; ferrierite-Mg, -K, -Na; gmelinite-Na, -Ca, -K; heulandite-Ca, -Na, -K, -Sr; levyne-Ca, -Na; paulingite-K, -Ca; phillipsite-Na, -Ca, -K stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data, IZA structure-type symbols, space-group symmetry, unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral

  20. CRYSTAL CHEMISTRY OF HYDROUS MINERALS

    SciTech Connect

    Y. ZHAO; ET AL

    2001-02-01

    Hydrogen has long been appreciated for its role in geological processes of the Earth's crust. However, its role in Earth's deep interior has been neglected in most geophysical thinking. Yet it is now believed that most of our planet's hydrogen may be locked up in high pressure phases of hydrous silicate minerals within the Earth's mantle. This rocky interior (approximately 7/8 of Earth's volume) is conjectured to contain 1-2 orders of magnitude more water than the more obvious oceans (the ''hydrosphere'') and atmosphere. This project is aimed at using the capability of neutron scattering from hydrogen to study the crystal chemistry and stability of hydrogen-bearing minerals at high pressures and temperatures. At the most basic level this is a study of the atomic position and hydrogen bond itself. We have conducted experimental runs on hydrous minerals under high pressure and high temperature conditions. The crystallographic structure of hydrous minerals at extreme conditions and its structural stability, and hydrogen bond at high P-T conditions are the fundamental questions to be addressed. The behavior of the hydrous minerals in the deep interior of the Earth has been discussed.

  1. Traditional Methods for Mineral Analysis

    NASA Astrophysics Data System (ADS)

    Ward, Robert E.; Carpenter, Charles E.

    This chapter describes traditional methods for analysis of minerals involving titrimetric and colorimetric procedures, and the use of ion selective electrodes. Other traditional methods of mineral analysis include gravimetric titration (i.e., insoluble forms of minerals are precipitated, rinse, dried, and weighed) and redox reactions (i.e., mineral is part of an oxidation-reduction reaction, and product is quantitated). However, these latter two methods will not be covered because they currently are used little in the food industry. The traditional methods that will be described have maintained widespread usage in the food industry despite the development of more modern instrumentation such as atomic absorption spectroscopy and inductively coupled plasma-atomic emission spectroscopy (Chap. 24). Traditional methods generally require chemicals and equipment that are routinely available in an analytical laboratory and are within the experience of most laboratory technicians. Additionally, traditional methods often form the basis for rapid analysis kits (e.g., Quantab®; for salt determination) that are increasingly in demand. Procedures for analysis of minerals of major nutritional or food processing concern are used for illustrative purposes. For additional examples of traditional methods refer to references (1-6). Slight modifications of these traditional methods are often needed for specific foodstuffs to minimize interferences or to be in the range of analytical performance. For analytical requirements for specific foods see the Official Methods of Analysis of AOAC International (5) and related official methods (6).

  2. Hyperspectral analysis of clay minerals

    NASA Astrophysics Data System (ADS)

    Janaki Rama Suresh, G.; Sreenivas, K.; Sivasamy, R.

    2014-11-01

    A study was carried out by collecting soil samples from parts of Gwalior and Shivpuri district, Madhya Pradesh in order to assess the dominant clay mineral of these soils using hyperspectral data, as 0.4 to 2.5 μm spectral range provides abundant and unique information about many important earth-surface minerals. Understanding the spectral response along with the soil chemical properties can provide important clues for retrieval of mineralogical soil properties. The soil samples were collected based on stratified random sampling approach and dominant clay minerals were identified through XRD analysis. The absorption feature parameters like depth, width, area and asymmetry of the absorption peaks were derived from spectral profile of soil samples through DISPEC tool. The derived absorption feature parameters were used as inputs for modelling the dominant soil clay mineral present in the unknown samples using Random forest approach which resulted in kappa accuracy of 0.795. Besides, an attempt was made to classify the Hyperion data using Spectral Angle Mapper (SAM) algorithm with an overall accuracy of 68.43 %. Results showed that kaolinite was the dominant mineral present in the soils followed by montmorillonite in the study area.

  3. Understanding mineral dusts from the Middle East

    NASA Astrophysics Data System (ADS)

    Engelbrecht, J. P.; McDonald, E.; Gillies, J. A.; Jayanty, J.; Casuccio, G.; Gertler, A.

    2012-12-01

    The purpose of the program was to provide scientifically founded information on the chemical and physical properties of airborne mineral dust collected during a period of approximately one year, largely in 2006, at Djibouti, Afghanistan (Bagram, Khowst), Qatar, United Arab Emirates, Iraq (Balad, Baghdad, Tallil, Tikrit, Taji, Al Asad), and Kuwait (Northern, Central, Coastal, and Southern regions). To fully understand mineral dusts, their chemical and physical properties as well as mineralogical interrelationships were accurately established. Three collocated low volume particulate samplers, one each for the total suspended (TSP), less than 10 μm in aerodynamic diameter (PM10), and less than 2.5 μm in aerodynamic diameter (PM2.5) particulate matter were deployed at each of the 15 sites, operating on a "1 in 6 day" sampling schedule. A total of 3,136 filter samples were collected on a 1-in-6 day schedule, along with one-time bulk soil samples, at each of the 15 sites. Sample media included Teflon® membrane and quartz fiber filters for chemical analysis (71 species), and Nuclepore® filters for individual particle analysis by Scanning Electron Microscopy (SEM). The provisional study of the data revealed three broad air pollution sources: geological dust, smoke from burn pits, and until now unidentified lead-zinc smelters and battery-processing facilities. SEM results and secondary electron imagery show that quartz and other silicate minerals and, to a lesser extent, dolomite and calcite particles are coated by a thin Si-Al-Mg layer, probably the clay minerals palygorskite and/or montmorillonite/illite. Positive Matrix Factorization (PMF) was performed on aerosol samples collected at six military sites in Iraq (Balad, Baghdad, Tallil, Tikrit, Taji, and Al Asad). PMF results reflect chemical differences amongst sources impacting at individual sites, further complicated by the regional geomorphology and meteorology. Sampling sites are seldom impacted by one source at

  4. Respiratory disability in coal miners

    SciTech Connect

    Morgan, W.K.C.; Lapp, N.L.; Seaton, D.

    1980-06-20

    It has been suggested that the assessment of ventilatory capacity alone is inadequate for the determination of disabling occupational respiratory impairment in coal miners. The Department of Labor has accepted this view and now routinely requests blood gas analyses in those claimants not meeting the ventilatory criteria. We tested the validity of this contention by selecting two groups of coal miners claiming total disability. The first consisted of 150 claimants who were referred for spirometry, while the second consisted of 50 claimants who had been referred for blood gas studies. Of those in group 1, eight met the extant criteria for disability, while only two of those in group 2 satisfied the criteria, and, in both, cardiac disease was responsible. We conclude that blood gas analyses are unnecessary in the determination of pulmonary disability in coal miners.

  5. 43 CFR 3873.1 - Segregation of mineral from non-mineral land.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false Segregation of mineral from non-mineral...) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) ADVERSE CLAIMS, PROTESTS AND CONFLICTS Segregation § 3873.1 Segregation of mineral from non-mineral land. Where a survey...

  6. 43 CFR 3873.1 - Segregation of mineral from non-mineral land.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false Segregation of mineral from non-mineral...) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) ADVERSE CLAIMS, PROTESTS AND CONFLICTS Segregation § 3873.1 Segregation of mineral from non-mineral land. Where a survey...

  7. 43 CFR 3873.1 - Segregation of mineral from non-mineral land.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false Segregation of mineral from non-mineral...) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) ADVERSE CLAIMS, PROTESTS AND CONFLICTS Segregation § 3873.1 Segregation of mineral from non-mineral land. Where a survey...

  8. 43 CFR 3873.1 - Segregation of mineral from non-mineral land.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false Segregation of mineral from non-mineral...) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000) ADVERSE CLAIMS, PROTESTS AND CONFLICTS Segregation § 3873.1 Segregation of mineral from non-mineral land. Where a survey...

  9. Geochemical processes at mineral surfaces

    SciTech Connect

    Davis, J.A.; Hayes, K.F.

    1986-01-01

    This volume includes 32 papers which were presented at a symposium on geochemical processes at mineral-water interfaces in 1985 and which bring to bear on this area a very wide range of expertise. The discontinuities in properties which occur at the mineral-water interface have profound effects on the movement of naturally occurring ions. Weathering and precipitation processes control the concentrations and speciation of ions in natural waters and the movements of these within the hydrosphere; both classes of processes take place at mineral-water interfaces. After an introductory overview, the book is divided into seven major sections, each dealing with one of the aspects of the processes occurring at the mineral-water interface. Five papers deal with the physical properties of the mineral-water interface; these represent a well-balanced mix of experimental and theoretical (mathematical modeling) work. Adsorption phenomena are dealt with in another five papers; these are largely experimental in character. Ion-exchange processes are discussed in four papers, one of which addresses the use of relaxation methods to study ion exchange kinetics at the microscopic level. Spectroscopic techniques (including electron-spin resonance and Moessbauer spectroscopy) are utilized in four papers. Chemical reactions, mainly redox processes, at mineral-water interfaces are treated in four papers, one of which deals with non-biological organic reactions. Solid-solution formation and equilibria are the subjects of another set of four articles, and the last group of papers deals with the processes involved in precipitation and dissolution, including weathering.

  10. Metamorphism and gold mineralization in the Blue Ridge, Southernmost Appalachians

    USGS Publications Warehouse

    Stowell, H.H.; Lesher, C.M.; Green, N.L.; Sha, P.; Guthrie, G.M.; Sinha, A.K.

    1996-01-01

    Lode gold mineralization in the Blue Ridge of the southernmost Appalachians is hosted by metavolcanic rocks (e.g., Anna Howe mine, AL; Royal Vindicator mine, GA), metaplutonic rocks (e.g., Hog Mountain mine, AL), and metasedimentary rocks (e.g., Lowe, Tallapoosa, and Jones Vein mines, AL). Most gold occurs in synkinematic quartz ?? plagioclase ?? pyrite ?? pyrrhotite ?? chlorite veins localized along polydeformational faults that juxtapose rocks with significantly different peak metamorphic mineral assemblages. Mineralogy, chemistry, and O and H isotope studies suggest that the three types of host rocks have undergone differing amounts and types of alteration during mineralization. Limited wall-rock alteration in metavolcanic- and metasediment-hosted deposits, and relatively extensive wall-rock alteration in granitoid-hosted deposits, suggests that most deposits formed from fluids that were close to equilibrium with metavolcanic and metasedimentary rocks. Stable isotope compositions of the fluids calculated from vein minerals and vein selvages are consistent with a predominantly metasedimentary fluid source, but vary from deposit to deposit (-22 to -47??? ??D, 4-5??? ??18O, and 5-7??? ??34S at Anna Howe and Royal Vindicator; -48 to -50??? ??D, 9-13??? ??18O, and ca. 19??? ??34S at Lowe and Jones Vein; and -22 to -23??? ??D, 8-11??? ??18O, 9-10??? ??34S, and -6 ??13C at Hog Mountain). Silicate mineral thermobarometry of vein, vein selvage, and wall-rock mineral assemblages indicate that mineralization and regional metamorphism occured at greenschist to amphibolite facies (480?? ?? 75??C at Anna Howe, 535?? ?? 50??C at 6.4 ?? 1 kbars at Lowe, 530?? ?? 50??C at 6.9 ?? 1 kbars at Tallapoosa, and 460?? ?? 50??C at 5.5 ?? 1 kbars at Hog Mountain). Oxygen isotope fractionation between vein minerals and selvage minerals consistently records equilibration temperatures that are similar to or slightly lower than those estimated from silicate thermometry. Auriferous veins

  11. Wollastonite : a versatile industrial mineral

    USGS Publications Warehouse

    ,

    2001-01-01

    Wollastonite is a chemically simple mineral named in honor of English mineralogist and chemist Sir W.H. Wollaston (1766–1828). It is composed of calcium (Ca) and silicon and oxygen (SiO2, silica) with the chemical formula CaSiO3. Although much wollastonite is relatively pure CaSiO3, it can contain some iron, magnesium, manganese, aluminum, potassium, sodium, or strontium substituting for calcium in the mineral structure. Pure wollastonite is bright white; the type and amount of impurities can produce gray, cream, brown, palegreen, or red colors.

  12. Abu al-Layth al-Libi

    DTIC Science & Technology

    2015-02-01

    Introduction In the tradition of post-9/11 senior Arab militant figures operating in Khurasan (the Afghanistan-Pakistan region), there is little doubt as to...the standing of Libyan jihadi commander Abu al-Layth al-Libi. If Usama bin Ladin and Ayman al-Zawahiri came to be the most prominent Arab -Afghan...Libi, a longtime leader of the Libyan Islamic Fighting Group (LIFG), who rapidly established himself as the champion of the Arab -Afghan milieu after

  13. Reactivity of clay minerals with acids and alkalies

    USGS Publications Warehouse

    Carroll, D.; Starkey, H.C.

    1971-01-01

    One-g samples of a montmorillonite, a metabentonite, an illite, two kaolinites, and three halloysites were treated with 50 ml of hydrochloric acid (6??45 N, 1:1), acetic acid (4??5 N, 1:3), sodium hydroxide (2??8 N), sodium chloride solution (pH 6??10; Na = 35???; Cl = 21??5???), and natural sea water (pH 7??85; Na = 35??5???; Cl = 21??5???) for a 10-day period in stoppered plastic vials. The supernatant solutions were removed from the clay minerals and analyzed for SiO2, Al2O3, CaO, MgO, Na2O, and K2O. All the solutions removed some SiO2, Al2O3, and Fe2O3 from the samples, but the quantities were small. Sodium hydroxide attacked the kaolin group minerals more strongly than it did montmorillonite, metabentonite, or illite. Halloysite was more strongly attacked by hydrochloric acid than was any of the other experimental minerals. Hydrochloric acid removed iron oxide coatings from soil clay minerals, but acetic acid did not remove them completely. The samples most strongly attacked by HCl and NaOH were examined by X-ray diffraction. Acid treatment did not destroy the structure of the clays, but the halloysite structure was partially destroyed. Sodium hydroxide attacked the halloysite structure, as shown by chemical analysis and X-ray diffraction. These experiments show that treatment in dilute acids has no harmful effect in the preparation of clays for X-ray diffraction. Acetic acid is preferred to hydrochloric acid for this purpose. Hydrochloric acid cleans clay minerals by removing free iron oxide from the surface; acetic acid is less effective. ?? 1971.

  14. Nuclear Melt Glass Dissolution and Secondary Mineral Precipitation at 40 to 200C

    SciTech Connect

    Zavarin, M; Roberts, S; Viani, B; Pawloski, G; Rose, T

    2004-06-14

    Most long-lived radionuclides associated with an underground nuclear test are initially incorporated into melt glass and become part of the hydrologic source term (HST) only upon their release via glass dissolution (Pawloski et al., 2001). As the melt glass dissolves, secondary minerals precipitate. The types of secondary minerals that precipitate influence the water chemistry in and around the melt glass. The secondary minerals also provide a sorption sink to the released radionuclides. The changing water chemistry affects the rate of glass dissolution; it also affects the sorption behavior of the released radionuclides. This complex nature of glass dissolution and its important role in defining the HST requires a thorough understanding of glass dissolution and secondary mineral precipitation. The identity of secondary minerals formed at temperatures from 40 to 200 C are evaluated in this report to assist in that understanding.

  15. Can the dissolution rates of individual minerals be used to describe whole rock dissolution?

    NASA Astrophysics Data System (ADS)

    Critelli, Teresa; Marini, Luigi; Schott, Jacques; Mavromatis, Vasileios; Apollaro, Carmine; Rinder, Thomas; De Rosa, Rosanna; Oelkers, Eric H.

    2014-05-01

    There have been an exhaustive number of laboratory studies determining the dissolution rates of individual minerals, but few have focused on the dissolution rates of minerals in multi-mineralic rocks. As a result, geochemical modeling of the temporal evolution of water-rock interaction is generally based on the assumption that the dissolution rate of minerals within a rock is equal to that measured in the laboratory on individual minerals. To verify this hypothesis, we have determined experimentally the dissolution rates of a well characterized metabasalt rock (Apollaro et al., 2011; Bloise et al., 2012) from the Mt. Reventino area (Southern Italy) at 25°C in mixed flow reactors. From these experiments and rock modal analysis we have deduced the dissolution rates of the minerals present in the rock (actinolite, albite, chlorite, epidote, and phengite). The major observation of this effort include: (i) only small differences in the dissolution rates of the individual minerals were observed; these rates are close to the whole-rock dissolution rate and (ii) the dissolution rates of albite and chlorite are in close agreement with laboratory rates obtained from individual mineral dissolution experiments, whereas those of actinolite, phengite, and epidote are not consistent with those reported in literature by 1-2 orders of magnitude. These results demonstrate that the dissolution rate of a given mineral in a multi-phase rock can be affected by the presence of the other minerals. Rock dissolution kinetics are likely constrained by the dissolution rates of the more abundant, lesser reactive mineral or minerals in the rock. These unreactive minerals can prevent the dissolution of the more rapidly dissolving mineral grains by keeping them out of contact with the aqueous phase. This implies that the overall weathering rate of rocks cannot be modelled from the measured dissolution rates of its individual minerals. If confirmed through further studies, this conclusion may

  16. MX Siting Investigation. Mineral Resources Survey, Seven Additional Valleys, Nevada/Utah Siting Area. Volume II.

    DTIC Science & Technology

    1981-06-23

    AO-AI13 14𔃾 ERTEC WESTERN INC LONG BEACH CA F/6 7/4 MX SITING INVESTIGATION. MINERAL RESOURCES SURVEY, SEVEN ADDITI-ETC(U) JUN Al F04704-80-C-OGO6...DTIC-DDA-2 FORM DOCUMENT PROCESSING SHEET DTIC ocT :g 70A -- ~’ .9 ’I K ii I / "~1 - i~ / . . ..1’ ~ ~- .. ~ ~1 I E-TR-50 MINERAL RESOURCES SURVEY...144 ERTEC WESTERN INC. LONG BEACH CA F/6 7/4 MX SITING INVESTIGATION. MINERAL RESOURCES SURVEY. SEVEN AOOITI-ETCIU) JUN 81 FON7O-80-C-0006

  17. Mysterious Lava Mineral on Mars

    NASA Technical Reports Server (NTRS)

    2004-01-01

    This graph or spectrum captured by the Moessbauer spectrometer onboard the Mars Exploration Rover Spirit shows the presence of three different iron-bearing minerals in the soil at the rover's landing site. One of these minerals has been identified as olivine, a shiny green rock commonly found in lava on Earth. The other two have yet to be pinned down. Scientists were puzzled by the discovery of olivine because it implies the soil consists at least partially of ground up rocks that have not been weathered or chemically altered. The black line in this graph represents the original data; the three colored regions denote individual minerals and add up to equal the black line.

    The Moessbauer spectrometer uses two pieces of radioactive cobalt-57, each about the size of pencil erasers, to determine with a high degree of accuracy the composition and abundance of iron-bearing minerals in martian rocks and soil. It is located on the rover's instrument deployment device, or 'arm.'

  18. Mineral of the month: indium

    USGS Publications Warehouse

    George, Micheal W.

    2004-01-01

    Indium was discovered in Germany in 1863. Although it is a lustrous silver-white color, the finders named the new material for the “indigo” spectral lines the mineral created on the spectrograph. Indium ranks 61st in abundance in Earth’s crust and is about three times more abundant than silver or mercury.

  19. Mineral of the month: titanium

    USGS Publications Warehouse

    Gambogi, Joseph

    2004-01-01

    From paint to airplanes, titanium is important in a number of applications. Commercial production comes from titanium-bearing ilmenite, rutile and leucoxene (altered ilmenite). These minerals are used to produce titanium dioxide pigment, as well as an assortment of metal and chemical products.

  20. Mineral of the month: rhenium

    USGS Publications Warehouse

    Magyar, Michael J.

    2005-01-01

    Rhenium, an exotic, heat-resistant metal, has grown in importance since its discovery nearly 80 years ago. First isolated by a team of German chemists studying a platinum ore, the mineral was named for the Rhine River. From then until the 1960s, only 2 metric tons of rhenium were produced worldwide. In 2004, worldwide production was 40 metric tons.

  1. Mineral of the month: aggregates

    USGS Publications Warehouse

    Tepordei, Valentin V.

    2005-01-01

    Natural aggregates, consisting of crushed stone, and sand and gravel, are a major contributor to economic health, and have an amazing variety of uses. Aggregates are among the most abundant mineral resources and are major basic raw materials used by construction, agriculture and other industries that employ complex chemical and metallurgical processes.

  2. Mineral of the month: boron

    USGS Publications Warehouse

    Lyday, Phyllis A.

    2005-01-01

    What does boron have to do with baseball, apple pie, motherhood and Chevrolet? Boron minerals and chemicals are used in the tanning of leather baseballs and gloves; in micro-fertilizer to grow apples and in the glass and enamels of bakewares to cook apple pie; in boron detergents for soaking baby clothes and diapers; and in fiberglass parts for the Chevrolet Corvette.

  3. Mineral evolution and Earth history

    USGS Publications Warehouse

    Bradley, Dwight C.

    2015-01-01

    The field of mineral evolution—a merger of mineralogy and Earth history—coalesced in 2008 with the first of several global syntheses by Robert Hazen and coworkers in the American Mineralogist. They showed that the cumulative abundance of mineral species has a stepwise trend with first appearances tied to various transitions in Earth history such as the end of planetary accretion at ca. 4.55 Ga and the onset of bio-mediated mineralogy at ca. >2.5 Ga. A global age distribution is best established for zircon. Observed abundance of zircon fluctuates through more than an order of magnitude during successive supercontinent cycles. The pulse of the Earth is also recorded, albeit imperfectly, by the 87Sr/86Sr composition of marine biogenic calcite; the Sr-isotopic ratio of this mineral reflects the balance of inputs of primitive strontium at mid-ocean ridges and evolved strontium that drains off the continents. A global mineral evolution database, currently in the works, will greatly facilitate the compilation and analysis of extant data and the expansion of research in mineralogy outside its traditional bounds and into more interdisciplinary realms.

  4. IR spectroscopic determination of OH defects in spinel group minerals

    NASA Astrophysics Data System (ADS)

    Halmer, M. M.; Libowitzky, E.; Beran, A.

    2003-04-01

    Previous experimental studies showed that spinel phases, likely to occur in the transition zone of the Earth's mantle, contain essential amounts of water in form of OH groups. The g-Mg_2SiO_4 phase is reported to contain 27000 wt.ppm H_2O. The corresponding IR spectrum shows very broad absorption bands centered at 3645 and 3345cm-1 with a shoulder at 3120cm-1 (Kohlstedt et al., 1996). Thus, it is evident that under high-pressure conditions the spinel structure is capable to incorporate OH groups. Up to present, hydrogen contents of spinels from upper Earth's mantle and from crustal occurrences have not been reported in the literature. It is the aim of this study to prove the presence of OH defects in spinels of naturally occurring paragenesis and to develop some ideas on the structural incorporation mode based on promising results obtained from synthetic phases. Highly disordered non-stoichiometric Verneuil-grown MgAl spinels are characterized by two significant bands centered at 3355cm-1 and 3510cm-1, which show variations in band intensities. Synthetic H_ high-temperature treated intermediate compounds in the spinel-magnesioferrite (MgFe_2O_4), spinel-hercynite (FeAl2O4) and spinel-franklinite (ZnFe2O4) system from Andreozzi et al. (2001) indicate variable behavior. Whereas some of the spectra, which may be also correlated to d-d transitions of IVFe2+ (Skogby and Halenius, 2003) show broad absorptions in the 3500-3100cm-1 range, a pure MgAl2O4 end member sample is characterized by a rather sharp mode at 3450cm-1. Naturally occurring gahnite crystals (ZnAl2O_4) show significantly broad absorption band at 3400cm-1, which resembles some of the bands of the former synthetic samples. Based on the calibration of Libowitzky and Rossman (1997) the analytical H_2O content of the natural gahnite sample was determined to 580 wt.ppm. The position of the absorption bands implies weak hydrogen bonding of the OH defects in the spinel structure. This work was partly supported by

  5. Detrital shocked minerals: microstructural provenance indicators of impact craters

    NASA Astrophysics Data System (ADS)

    Cavosie, A. J.

    2014-12-01

    The study of detrital shocked minerals (DSMs) merges planetary science, sedimentology, mineralogy/crystallography, accessory mineral geochemistry, and geochronology, with the goal of identifying and determining provenance of shock metamorphosed sand grains. Diagnostic high-pressure impact-generated microstructures (planar fractures, planar deformation features) are readily identified on external grain surfaces using standard SEM imaging methods (BSE), and when found, unambiguously confirm an impact origin for a given sand grain. DSMs, including quartz, zircon, monazite, and apatite, have thus far been documented at the Vredefort Dome [1,2,3], Sudbury [4], Rock Elm [5], and Santa Fe [6,7] impact structures. DSMs have been identified in alluvium, colluvium, beach sand, and glacial deposits. Two main processes are recognized that imply the global siliciclastic record contains DSMs: they survive extreme distal transport, and they survive 'deep time' lithification. Distal transport: In South Africa, shocked minerals are preserved in alluvium from the Vaal River >750 km downstream from the Vredefort impact; SHRIMP U-Pb geochronology has confirmed the origin of detrital shocked zircon and monazite from shocked Vredefort bedrock [2]. Vredefort-derived shocked zircons have also been found at the mouth of the Orange River on the Atlantic coast, having travelled ~2000 km downriver from Vredefort [8]. Deep time preservation: Vredefort-derived shocked zircon and quartz has been documented in glacial diamictite from the 300 Myr-old Dwyka Group in South Africa. Shocked minerals were thus entrained and transported in Paleozoic ice sheets that passed over Vredefort [9]. An impact crater can thus be viewed as a unique 'point source', in some cases for billions of years [2,4]; DSMs thus have applications in studying eroded impact craters, sedimentary provenance, landscape evolution, and long-term sediment transport processes throughout the geologic record. This work was supported by

  6. Microbial mat mineralization in Great Salt Lake (Utah, USA)

    NASA Astrophysics Data System (ADS)

    PACE, Aurélie; Bouton, Anthony; Bourillot, Raphaël; Vennin, Emmanuelle; Visscher, Pieter; Dupraz, Christophe; Thomazo, Christophe; Serge, Galaup; Sophie, Leleu; Anna, Kwasniewski; Léa, Pigot; Michel, Franceschi

    2015-04-01

    Great Salt Lake is located in the Basin and Range province of Utah (USA). Its average surface is 4480 Km2 and its maximum depth is of about 15m. It is a partly rainfed endorheic hypersaline lake (average salinity: 140g/L). Due to the high salinity, little or no grazing organisms are present, favoring the development of microbialites that cover the margin of the lake. This work aims to understand the products and processes of mineralization in recent and modern microbialites on the western margin of Antelope Island. The distribution of microbialites and their morphology has been studied along lakeshore to center transects, showing a contrasting spatial distribution in bay versus headland. Fossil microbialites show a great diversity of macro- and microfabrics, some microbialites being essentially built by microbial-mediated carbonate precipitation, while other show the predominance of trapping and binding processes. The nature and composition of the microbial carbonates have been determined through polarizing, cathodoluminescence, reflected fluorescence microscopy, X-Ray diffractometry and isotope geochemistry (δ 18O and δ13C) in order to investigate the preservation of environmental signals in microbialites. Petrophysics analysis such as permeability and porosimetry, have been done to observe the structure of the microbialite. Microprobe and silver foils method have been used respectively to characterize oxygen production and sulfate reduction in living microbial mats. Mineralization zones seem to coincide with sulfate reduction hotspots. This mineralization results in mixed clotted-laminated fabric at the macro- and microscale. Several analysis such as Cryo-SEM, environmental SEM and raman spectroscopy three phases of mineralization allowed us to distinguish three type of minerals inside the mat: (1) a Mg and Si-rich clay developing on the organic matrix; (2) an intracellular Al-rich clay. (3) aragonite clots replacing the organic matrixes and embedding bacteria

  7. Organo-mineral Interactions in Ultisols and Andosols with Contrasting Mineralogy

    NASA Astrophysics Data System (ADS)

    Sparks, D. L.

    2015-12-01

    Organo-mineral associations play an important role in long-term stabilization of soil organic matter. To understand the role of soil minerals and major cations in organo-mineral interactions, we applied STXM-NEXAFS spectroscopy at C, N, Al and Si K-edges, as well as Ca and Fe L-edges, to conduct submicron-level investigations of the associations of C and C forms with Ca, Fe, Al and Si in soil clay fraction of Ultisols and Andosols with contrasting mineralogy. Ultisols were under agricultural use receiving input of limestone and mushroom compost, whereas Andosols were under natural vegetation. The poorly crystalline minerals such as allophane and ferrihydrite were rich in Andosols, while Ultisols were dominated by vermiculite, illite and kaolinite. STXM analysis showed a high spatial correlation between C and Ca in the Utisols. The major Ca forms in agricultural Ultisols were organic Ca. A variety of C forms such as phenols, heterocyclic compounds, carboxylamides were found in Ca-rich "hot spots" in Ultisols. In contrast a relatively uniform distribution of C and C forms on mineral surfaces was observed in Andosols, revolutionizing our view of heterogeneous distribution of OM in natural soil. The C forms associated with minerals were aromatic and carboxyl C. These results demonstrates the importance of Ca containing organic compounds in soil C sequestration in agricultural Ultisols, and highlights the important role of the poorly-crystalline soil minerals in soil organic matter sequestration in Andosols.

  8. Elastic Properties of Mantle Minerals

    NASA Astrophysics Data System (ADS)

    Duffy, T. S.; Stan, C. V.

    2012-12-01

    The most direct information about the interior structure of the Earth comes from seismic wave velocities. Interpretation of seismic data requires an understanding of how sound velocities and elastic properties of minerals vary with pressure, temperature, crystal structure, and composition as well as the role of anelasticity, melts, etc. More generally, elastic moduli are important for understanding many solid-state phenomena including mechanical stability, interatomic interactions, material strength, compressibility, and phase transition mechanisms. The database of mineral elasticity measurements has been growing rapidly in recent years. In this work, we report initial results of an ongoing survey of our current knowledge of mineral elasticity at both ambient conditions and high pressures and temperatures. The analysis is selective, emphasizing single crystal measurements but also incorporating polycrystalline measurements and volume compression data as appropriate. The goal is to synthesize our current understanding of mineral elasticity in terms of structure and composition, and to identify the major remaining needs for experimental and theoretical work. Clinopyroxenes (Cpx) provide an example of our approach. A wide range of clinopyroxene compositions are found geologically and Mg-, Ca-, and Na-rich clinopyroxenes are expected to be important components in the upper mantle. The single-crystal elastic properties of a number of endmember Cpx compositions have been measured and these exhibit a range of ~25% in shear velocity. Those with monovalent cations (spodumene, jadeite) in the M2 site exhibit the highest velocities while Fe-rich (hendenbergit, acmite) compositions have the lowest velocities. The effects on velocity due to a wide range of chemical substitutions can be defined, but there are important discrepancies and omissions in the database. New measurements of omphacites, intermediate diopside-hedenbergite compositions, aegerine/acmite, augite, etc. are

  9. Interfacial tension between immiscible melts in the system K2O - FeO - Fe2O3 - Al2O3 - SiO2

    NASA Astrophysics Data System (ADS)

    Kaehn, J.; Veksler, I. V.; Franz, G.; Dingwell, D. B.

    2009-12-01

    and Kohlstedt, 1991), or 20-40 times lower than the surface tension of natural lavas in air (Walker and Mullins, 1981). Interfacial tension between natural, less compositionally contrasting ferrobasaltic and rhyolitic melts should be even lower by a factor of 2 or 3. Very low interfacial tension implies easy nucleation of immiscible liquid droplets, and very slow coarsening of silicate emulsions. The results of interfacial tension measurements corroborate protracted stability of sub-micron immiscible silicate emulsions that we observed in our previous immiscibility experiments. References Naslund H.R. (1983) Am. J. Sci. 283, 1034-1059. Philpotts A.R. (1982) Contrib. Mineral. Petrol. 80, 201-218. Walker D. and Mullins Jr. O. (1981) Contrib. Mineral. Petrol. 76, 455-462. Wanamaker B.J. and Kohlstedt D.L. (1991) Phys. Chem. Minerals, 18, 26-36.

  10. Genesis and evolution of the Baid al Jimalah tungsten deposit, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Kamilli, Robert J.

    1986-01-01

    Baid al Jimalah is similar in character and origin to other tungsten-tin greisen deposits in the world, especially the Hemerdon deposit in Devon, England. It is also analogous to Climax-type molybdenum deposits, which contain virtually identical mineral assemblages, but with the relative intensities of the molybdenum and tungsten mineralization reversed.

  11. Mineral dissolution and secondary precipitation on quartz sand in simulated Hanford tank solutions affecting subsurface porosity

    NASA Astrophysics Data System (ADS)

    Wang, Guohui; Um, Wooyong

    2012-11-01

    Highly alkaline nuclear waste solutions have been released from underground nuclear waste storage tanks and pipelines into the vadose zone at the US Department of Energy's Hanford Site in Washington, causing mineral dissolution and re-precipitation upon contact with subsurface sediments. High pH caustic NaNO3 solutions with and without dissolved Al were reacted with quartz sand through flow-through columns stepwise at 45, 51, and 89 °C to simulate possible reactions between leaked nuclear waste solution and primary subsurface mineral. Upon reaction, Si was released from the dissolution of quartz sand, and nitrate-cancrinite [Na8Si6Al6O24(NO3)2] precipitated on the quartz surface as a secondary mineral phase. Both steady-state dissolution and precipitation kinetics were quantified, and quartz dissolution apparent activation energy was determined. Mineral alteration through dissolution and precipitation processes results in pore volume and structure changes in the subsurface porous media. In this study, the column porosity increased up to 40.3% in the pure dissolution column when no dissolved Al was present in the leachate, whereas up to a 26.5% porosity decrease was found in columns where both dissolution and precipitation were observed because of the presence of Al in the input solution. The porosity change was also confirmed by calculation using the dissolution and precipitation rates and mineral volume changes.

  12. Mineral Dissolution and Secondary Precipitation on Quartz Sand in Simulated Hanford Tank Solutions Affecting Subsurface Porosity

    SciTech Connect

    Wang, Guohui; Um, Wooyong

    2012-11-23

    Highly alkaline nuclear waste solutions have been released from underground nuclear waste storage tanks and pipelines into the vadose zone at the U.S. Department of Energy’s Hanford Site in Washington, causing mineral dissolution and re-precipitation upon contact with subsurface sediments. High pH caustic NaNO3 solutions with and without dissolved Al were reacted with quartz sand through flow-through columns stepwise at 45, 51, and 89°C to simulate possible reactions between leaked nuclear waste solution and primary subsurface mineral. Upon reaction, Si was released from the dissolution of quartz sand, and nitrate-cancrinite [Na8Si6Al6O24(NO3)2] precipitated on the quartz surface as a secondary mineral phase. Both steady-state dissolution and precipitation kinetics were quantified, and quartz dissolution apparent activation energy was determined. Mineral alteration through dissolution and precipitation processes results in pore volume and structure changes in the subsurface porous media. In this study, the column porosity increased up to 40.3% in the pure dissolution column when no dissolved Al was present in the leachate, whereas up to a 26.5% porosity decrease was found in columns where both dissolution and precipitation were observed because of the presence of Al in the input solution. The porosity change was also confirmed by calculation using the dissolution and precipitation rates and mineral volume changes.

  13. U.S. Geological Survey Mineral Resources Program—Mineral resource science supporting informed decisionmaking

    USGS Publications Warehouse

    Wilkins, Aleeza M.; Doebrich, Jeff L.

    2016-09-19

    The USGS Mineral Resources Program (MRP) delivers unbiased science and information to increase understanding of mineral resource potential, production, and consumption, and how mineral resources interact with the environment. The MRP is the Federal Government’s sole source for this mineral resource science and information. Program goals are to (1) increase understanding of mineral resource formation, (2) provide mineral resource inventories and assessments, (3) broaden knowledge of the effects of mineral resources on the environment and society, and (4) provide analysis on the availability and reliability of mineral supplies.

  14. The geology of aluminium phosphates and sulphates of the alunite group minerals: a review

    NASA Astrophysics Data System (ADS)

    Dill, Harald G.

    2001-03-01

    Aluminium phosphates and sulphates of the alunite supergroup (APS minerals) occur in a wide range of environments of formation covering the metamorphic, igneous and sedimentary realms. Supergene processes, including mineral dressing and dumping when sulphide ores are mined, as well as hypogene alteration are also responsible for the precipitation of APS minerals. In these environments, complex solid solution series (s.s.s.) can form. The general formula of these alunite minerals is AB 3 (XO 4) 2(OH) 6, where A is a large cation (Na, U, K, Ag, NH 4, Pb, Ca, Ba, Sr, REE). B sites are occupied by cations of the elements Al, Fe, Cu and Zn. In nature, the anion (XO 4) x- is dominated by P and S. Mineral dressing and identification of APS minerals often needs a combination of highly sophisticated measures including Atterberg settling methods, XRD, DTA, TGA, TEM-EDX, SEM, EMPA and XRF. In sedimentary rocks APS minerals occur in various rocks and environments of deposition: calcareous, phosphorite-bearing, argillaceous-carbonaceous, arenaceous, coal-bearing environments, in soils and paleosols, in saprolite (bauxites, laterites) and in calcareous-argillaceous sequences hosting Carlin-type SHDG deposits. In igneous rocks, APS minerals may be encountered mainly in acidic through intermediate pyroclastic, volcanic and subvolcanic rocks. They occur in barren volcanic rocks and porphyry-type intrusions that have sparked epithermal Au-Ag-base metal deposits, Au-Sb mineralization, APS-bearing argillite and alunite deposits in their immediate surroundings. Granitic and pegmatitic rocks are rarely host of supergene APS mineralization. During low-grade stage regional metamorphism, peraluminous parent rocks originating from a sedimentary or igneous protolith may also give rise to APS mineralization. Peraluminous parent rocks enriched in S and/or P are a prerequisite for the formation of APS minerals that are stable up to a temperature of 400°C at moderately high fluid pressure of up

  15. Structure and physical properties of Hydrogrossular mineral series

    NASA Astrophysics Data System (ADS)

    Adhikari, Puja

    The mineral hydrogrossular series (Ca3Al2(SiO 4)3-x(OH)4x; 0 ≤ x ≤ 3) are important water bearing minerals found in the upper and lower part of the Earth's mantle. They are vital to the planet's hydrosphere under different hydrothermal conditions. The composition and structure of this mineral series are important in geoscience and share many commonalities with cement and clay materials. Other than the end members of the series x = 0 (grossular) and x = 3 (katoite) which have a cubic garnet structure, the structure of the series is totally unknown. We used large-scale ab initio modeling to investigate the structures and properties for hydrogrossular series for x = 0, 0.5, 1, 1.5, 2, 2.5, 3. Results indicate that for x > 0 and x < 3, the structures are tetragonal. This shows that there is structural change related to the lowering of overall symmetry associated with the composition of SiO4 tetrahedra and AlO6 octahedra. Total Bond order also explains the reason behind the change in the compressibility of the series. The electronic structure, mechanical and optical properties of the hydrogrossular series are calculated and the results for grossular and katoite are in good agreement with the available experimental data. The x--dependence of these physical properties for the series supports the notion of the aforementioned structural transition from cubic to tetragonal.

  16. Characterization and Thermodynamics Studies of Feldspar and Feldspathoid Minerals

    NASA Astrophysics Data System (ADS)

    Rudow, M.; Lilova, K.

    2015-12-01

    The application of thermal analysis and calorimetry for the studies of minerals has a history as long as the existence of the thermal methods themselves. New advanced calorimetric techniques have been developed for more accurate characterization of both bulk and nano materials thus impacting their design, processing, and applications. TG-DTA and TG-DSC are used to characterize the composition of complex minerals (e.g. [KxNa1-x(AlSi3)O8]) based on the weight changes and phase transformations observed with temperature increase. Additionally, those techniques allow to determine the quantity of the different types of water contained in natural feldspars and feldspathoids (absorbed, interlayer, structural). The results for several clays will be discussed. The geochemical properties and thermal stability of another class of minerals - aluminosilicate frameworks (alkali sodalities, natrolites, etc.) as related to high-level nuclear waste treatment facilities, radioactive waste storage and management were studied. The natural sodalite Na8[Al6Si6O24]Cl2 and similar frameworks with different anions are part of sodium-aluminosilicate (NAS) low activity radioactive waste produced during steam reforming process treatment. The enthalpies and entropies of formation and the hydration enthalpies of the above-mentioned feltspathoids are obtained and the effect of the different cations and anions on the thermodynamic stability was studied. The results will allow to predict the long term behavior of the compounds in the environment under different conditions.

  17. Exchangeable and secondary mineral reactive pools of aluminium in coastal lowland acid sulfate soils.

    PubMed

    Yvanes-Giuliani, Yliane A M; Waite, T David; Collins, Richard N

    2014-07-01

    The use of coastal floodplain sulfidic sediments for agricultural activities has resulted in the environmental degradation of many areas worldwide. The generation of acidity and transport of aluminium (Al) and other metals to adjacent aquatic systems are the main causes of adverse effects. Here, a five-step sequential extraction procedure (SEP) was applied to 30 coastal lowland acid sulfate soils (CLASS) from north-eastern New South Wales, Australia. This enabled quantification of the proportion of aluminium present in 'water-soluble', 'exchangeable', 'organically-complexed', 'reducible iron(III) (oxyhydr)oxide/hydroxysulfate-incorporated' and 'amorphous Al mineral' fractions. The first three extractions represented an average of 5% of 'aqua regia' extractable Al and their cumulative concentrations were extremely high, reaching up to 4000 mg·kg(-1). Comparison of Al concentrations in the final two extractions indicated that 'amorphous Al minerals' are quantitatively a much more important sink for the removal of aqueous Al derived from the acidic weathering of these soils than reducible Fe(III) minerals. Correlations were observed between soil pH, dissolved and total organic carbon (DOC and TOC) and Al concentrations in organic carbon-rich CLASS soil horizons. These results suggest that complexation of Al by dissolved organic matter significantly increases soluble Al concentrations at pH values >5.0. As such, present land management practices would benefit with redefinition of an 'optimal' soil from pH ≥5.5 to ~4.8 for the preservation of aquatic environments adjacent to organic-rich CLASS where Al is the sole or principle inorganic contaminant of concern. Furthermore, it was observed that currently-accepted standard procedures (i.e. 1 M KCl extraction) to measure exchangeable Al concentrations in these types of soils severely underestimate exchangeable Al and a more accurate representation may be obtained through the use of 0.2 M CuCl2.

  18. Authigenic Mineral Cycling in Roman Seawater Concrete with Campi Flegrei Pumiceous Ash Pozzolan

    NASA Astrophysics Data System (ADS)

    Jackson, M. D.; Mulcahy, S. R.; Chen, H.; Li, Q.; Cappelletti, P.; Carraro, C.; Wenk, H. R.

    2015-12-01

    Alteration of Campi Flegrei pumiceous ash in Roman concrete harbor structures along the central Italian coast produced zeolite and Ca-silicate minerals that have reinforced cementitious fabrics for >2000 years. X-ray microdiffraction experiments and electron microprobe analyses show that diverse alteration paths produced authigenic phillipsite and Al-tobermorite in the pyroclasts, pores, and cementing matrix of mortars in Romacons drill cores from Portus Cosanus, Portus Neronis, and Baianus Sinus. These minerals have cation exchange capabilities for some radionuclides and heavy metal cations and are candidate sorbents for concrete waste encapsulations. Compositions of phillipsite in certain Portus Cosanus and Portus Neronis pumice clasts are similar to those in the Neapolitan Yellow Tuff. Dissolution of this phillipsite and alkali feldspar produced new, authigenic phillipsite with less Si, greater Al and Ca, Al-tobermorite, and poorly-crystalline binder in pumice vesicles. Conversely, alteration of trachytic glass to clay mineral (nontronite) in a Baianus Sinus tuff clast is associated with new, authigenic phillipsite and Al-tobermorite in the tuff and cementing matrix. The Al-tobermorite has lower Al/(Si+Al) and Ca/(Si+Al) compared to Al-tobermorite in relict lime clasts. These more siliceous crystals, similar to those in hydrothermally-altered basalt, have 11.3 Å d-spacing in [001]. Raman spectra show symmetrical bending of Si-O-Si and Si-O-Al linkages, Si-O and Si-Al symmetrical stretching, and possible Q3 Si and Al tetrahedral peaks that suggest cross-linking of silicate chains-an important factor in cation exchange. The authigenic crystals refine pore space, contribute to binding in interfacial zones, and obstruct microcrack propagation. The well-constrained history of temperature variations and seawater immersion could provide further information for understanding alteration in volcanoclastic deposits and predicting regenerative processes in high performance

  19. [Treatment of infectious diseases in al-Andalus].

    PubMed

    Casal, M T; Casal, M

    2004-12-01

    The treatment used in Islamic Spain, al-Andalus, for a number of infectious diseases such as leprosy, tuberculosis, gonococcal disease, diarrhea, smallpox, measles, parasitic diseases, etc., is reviewed briefly. The different remedies of plant, animal and mineral extracts employed by renowned physicians of the time, such as Isaac, Arib ibn Said, Abulcasis, al-Gafiqi and Averroes among others, are analyzed briefly to provide an understanding of the approach to the treatment of infectious diseases nowadays known to be caused by microorganisms.

  20. Thermodynamics of Minerals Stable Near the Earth's Surface

    SciTech Connect

    Navrotsky, Alexandra

    2003-02-01

    OAK B262 Research & Education Activities We are working on developing calorimetric techniques for sulfide minerals. We have completed calorimetric studies of (Na, K, H3O) jarosites, of Na and K jarosite -alunite solid solutions, and of Cr6+ - containing jarosites. We are now working on phases containing As and Pb. These studies are important to issues of heavy metal pollution in the environment. A number of postdocs, graduate students, and undergrads have participated in the research. We have active collaboration with Dirk Baron, faculty at California State University, Bakersfield. In a collaboration with Peter Burns, Notre Dame University, we are working on thermochemistry of U6+ minerals. Navrotsky has participated in a number of national workshops that are helping to define the interfaces between nanotechnology and earth/environmental science. Major Findings Our first finding on uranyl minerals shows that studtite, a phase containing structural peroxide ion, is thermodynamically unstable in the absence of a source of aqueous peroxide ion but is thermodynamically stable in contact with a solution containing peroxide concentrations expected for the radiolysis of water in contact with spent nuclear fuel. This work is in press in Science. We have a consistent thermodynamic data set for the (Na, K, H3O) (Al, Fe) jarosite, alunite minerals and for Cr6+ substituting for S6+ in jarosite. The latter phases represent one of the few solid sinks for trapping toxic Cr6+ in groundwater. Contributions within Discipline Better understanding of thermodynamic driving for and constraints on geochemical and environmental processes.

  1. Np and Pu Sorption to Manganese Oxide Minerals

    SciTech Connect

    Zhao, P; Johnson, M R; Roberts, S K; Zavarin, M

    2005-08-30

    Manganese oxide minerals are a significant component of the fracture lining mineralogy at Yucca Mountain (Carlos et al., 1993) and within the tuff-confining unit at Yucca Flat (Prothro, 1998), Pahute Mesa (Drellack et al., 1997), and other locations at the Nevada Test Site (NTS). Radionuclide sorption to manganese oxide minerals was not included in recent Lawrence Livermore National Laboratory (LLNL) hydrologic source term (HST) models which attempt to predict the migration behavior of radionuclides away from underground nuclear tests. However, experiments performed for the Yucca Mountain Program suggest that these minerals may control much of the retardation of certain radionuclides, particularly Np and Pu (Triay et al., 1991; Duff et al., 1999). As a result, recent HST model results may significantly overpredict radionuclide transport away from underground nuclear tests. The sorption model used in HST calculations performed at LLNL includes sorption to iron oxide, calcite, zeolite, smectite, and mica minerals (Zavarin and Bruton 2004a; 2004b). For the majority of radiologic source term (RST) radionuclides, we believe that this accounts for the dominant sorption processes controlling transport. However, for the case of Np, sorption is rather weak to all but the iron and manganese oxides (Figure 1). Thus, we can expect to significantly reduce predicted Np transport by accounting for Np sorption to manganese oxides. Similarly, Pu has been shown to be predominantly associated with manganese oxides in Yucca Mountain fractured tuffs (Duff et al., 1999). Recent results on colloid-facilitated Pu transport (Kersting and Reimus, 2003) also suggest that manganese oxide coatings on fracture surfaces may compete with colloids for Pu, thus reducing the effects of colloid-facilitated Pu transport (Figure 1b). The available data suggest that it is important to incorporate Np and Pu sorption to manganese oxides in reactive transport models. However, few data are available for

  2. Effects of aluminum and nicotinic acid on bone minerals and growth in chicks

    SciTech Connect

    Johnson, N.E.; Dunn, M.A.; Ross, E.; Zierold, C. )

    1991-03-15

    One-day old Brown Leghorn-Cross male chicks were divided into three groups of ten chicks for each of the following experimental treatments: control; .05% Al and AlCl{sub 3}; 1.5% nicotinic acid (nic); .05% Al + 1.5% nic (Alnic). A standard corn-soybean meal chick starter diet served as the basal diet. Feed consumption and growth rates were recorded during the 14-day study. Chicks were sacrificed at the end of the study. Tibias were taken, weighed, ashed and dissolved in dilute acid. The acid digests were analyzed for mineral content (P, Ca, Mg, Fe, Zn) using induction-coupled-plasma emission spectroscopy. There were no significant differences between treatments based on mineral content per gram of bone. Bone weights of the Alnic group were decreased by 33% as compared to the control and all other groups; control being 6.49 {plus minus} 1.28g and Alnic being 4.37 {plus minus} 1.32. Body weight was decreased by 21% in the Alnic group. Although Al or nic had no effect on mineral content of bone, the combination of Al and nic caused a decrease in bone weight of the chicks. The combination was more toxic than administrative of either Al or nic alone. This finding may be relevant to the use of nicotinic acid as a supplement when Al containing substances are ingested at the same time.

  3. Mineral Resources, Geological Structure and Landform Surveys

    NASA Technical Reports Server (NTRS)

    Short, M. N.

    1973-01-01

    Significant results are presented of ERTS-1 investigations of landform surveys, mineral resources, and geological structures. The report covers four areas: (1) mapping investigations; (2) dynamic surface processes and landforms; (3) structural elements; and (4) mineral deposits.

  4. Mineral Resources, Economic Growth, and World Population

    ERIC Educational Resources Information Center

    Brooks, David B.; Andrews, P. W.

    1974-01-01

    World mineral supply and demand is discussed. The economics of future mineral availability in terms of effects on pollution, land use, energy consumption, human settlements, and the international distribution of income are emphasized. (DT)

  5. Effect of gallium on in vitro aortic valve cusp mineralization - EDXRF studies

    NASA Astrophysics Data System (ADS)

    Wróbel, A.; Goncerz, G.; Kunz, J.; Podolec, P.; Rokita, E.

    2004-01-01

    The present studies were designed to determine the effect of gallium on the aortic valve cusp mineralization. The studies were conducted on aortic valves collected at autopsy from 35 donors. Each sample was incubated for 21 days in the mineralization-promoting medium, containing Ga at concentrations ranging from 0.0 to 8.0 μg/ml. The elemental compositions of the samples were measured using energy dispersive X-ray fluorescence (EDXRF) method. The concentrations of 14 elements were determined: Mg, Al, S, Cl, K, Ca, Mn, Fe, Ni, Cu, Zn, Ga, Br and Sr. Calcium contents and Ca/P ratios were considered as markers of the mineralization process. The aortic valves could be divided into two groups depending on the advancement of the mineralization process. The first group in which the process progressed and the second one which was resistant to mineralization. Ga was accumulated in both groups. The results demonstrated that Ga reduced the aortic valve mineralization in dose-dependent manner in the first group and did not influence the mineralization in the mineralization-resistant aortic valves.

  6. /Cu-Al System

    NASA Astrophysics Data System (ADS)

    Kish, Orel; Froumin, Natalya; Aizenshtein, Michael; Frage, Nachum

    2014-05-01

    Wettability and interfacial interaction of the Ta2O5/Cu-Al system were studied. Pure Cu does not wet the Ta2O5 substrate, and improved spreading is achieved when relatively a high fraction of the active element (~40 at.% Al) was added. The Al2O3 and AlTaO4 phases were observed at the Ta2O5/Cu-Al interface. A thermodynamic evaluation allowed us to suggest that the lack of wetting bellow 40 at.% Al is due to the presence of a native oxide, which covers the drop. The conditions of the native oxide decomposition and the formation of the volatile Al2O suboxide strongly depend on the vacuum level during sessile drop experiments and the composition of the Cu-Al alloy. In our case, Al contents greater than 40% provides thermodynamic conditions for the formation of Al2O (as a result of Al reaction with Al2O3) and the drop spreading. It was suggested that the final contact angle in the Ta2O5/Cu-Al system (50°) is determined by Ta adsorption on the newly formed alumina interlayer.

  7. Re-evaluation of Non-regulatory Asbestos Group Minerals for Regulatory Agencies

    NASA Astrophysics Data System (ADS)

    Dogan, M.; Dogan, A.

    2013-05-01

    There are established rules and regulations for some asbestos group minerals - amphibole group minerals of actinolite, amosite, anthophyllite, crocidolite, tremolite; and serpentine group minerals of chrysotile- called "regulatory". There are also "non-regulatory" naturally occurring asbestos (NOA) group minerals as constituent of rocks and soil, including richterite, winchite, fluoro-edenite, balangeroite, carlosturanite, gageite, arfvedsonite, and magnesio-arfvedsonite. Strong evidences for carcinogenicity of these NOA minerals in later cohorts of cancer patients demonstrated the risks associated with these minerals. In addition, although the chrysotile asbestos regulated by some organizations such as WHO, World Trade Organization, United Nations, US EPA, International Labour Organization, and EU Countries; however, controversies still continue surrounding the use of chrysotile. Determinations of polymineralic fibrous veins, mixed particles, amphibole cleavage fragments, and genetic predisposition are also important issues (i.e. Dogan et al., 2006).Therefore, accurate characterizations of chemical composition, morphology, structure, and defects are necessary in order to find out mechanism(s) of carcinogenicity of all asbestos group minerals. Calculation methods of chemical composition are still under debate because of assumption of no vacancies at any sites and intergrowth of minerals. Substitution(s) may cause deviations from the ideal chemical formula and wide variations in chemical compositions. Detail morphological and chemical quantification of individual asbestos group minerals in micro- and nano-scale may help to evaluate its true carcinogenetic mechanism(s), and consequently prevention and possibly treatment of related diseases. we propose that nonregulatory asbestos minerals and the chrysotile should be re-evaluated. The amount of fibers inhaled, in terms of weight percent and number, need also be re-evaluated by mineralogists. Finally, Regulatory

  8. Strategic Minerals in the New World Order

    DTIC Science & Technology

    1993-11-30

    mineral scarcity does not exist; for an Neconomic price any product will be available in the world market. The domestic mining industry and those...shipping, and domestic mining industry efforts to establish subsidies for U.S. mineral production, using foreign flag hulls to import the minerals and...seeking to prevent further mining Industry damage; and those who saw the strategic minerals debate as but another politically incorrect effort to

  9. Mine and mineral occurrences of Afghanistan

    USGS Publications Warehouse

    Orris, G.J.; Bliss, J.D.

    2002-01-01

    This inventory of more than 1000 mines and mineral occurrences in Afghanistan was compiled from published literature and the files of project members of the National Industrial Minerals project of the U.S. Geological Survey. The compiled data have been edited for consistency and most duplicates have been deleted. The data cover metals, industrial minerals, coal, and peat. Listings in the table represent several levels of information, including mines, mineral showings, deposits, and pegmatite fields.

  10. Minerals yearbook, 1991: Massachusetts. Annual report

    SciTech Connect

    Harrison, D.K.; Sinnott, J.A.

    1993-05-01

    The value of nonfuel mineral production in 1991 was $111.6 million, a decrease of $16 million compared with the 1990 value. The decrease in 1991 was largely attributable to lower sales of construction sand and gravel and crushed stone, the State's two leading mineral commodities. Other mineral commodities produced included common clay, industrial sand, dimension stone, lime, and peat. Nationally, the State ranked 41st in the production of nonfuel minerals. It ranked fifth of 34 States that produced dimension stone.

  11. Nanoindentation hardness of mineralized tissues.

    PubMed

    Oyen, Michelle L

    2006-01-01

    A series elastic and plastic deformation model [Sakai, M., 1999. The Meyer hardness: a measure for plasticity? Journal of Materials Research 14(9), 3630-3639] is used to deconvolute the resistance to plastic deformation from the plane strain modulus and contact hardness parameters obtained in a nanoindentation test. Different functional dependencies of contact hardness on the plane strain modulus are examined. Plastic deformation resistance values are computed from the modulus and contact hardness for engineering materials and mineralized tissues. Elastic modulus and plastic deformation resistance parameters are used to calculate elastic and plastic deformation components, and to examine the partitioning of indentation deformation between elastic and plastic. Both the numerical values of plastic deformation resistance and the direct computation of deformation partitioning reveal the intermediate mechanical responses of mineralized composites when compared with homogeneous engineering materials.

  12. Initial Symptoms of ALS

    MedlinePlus

    ... Chapters Certified Centers and Clinics Support Groups About ALS About Us Our Research In Your Community Advocate ... Diagnosis En español Symptoms The initial symptoms of ALS can be quite varied in different people. One ...

  13. Lou Gehrig's Disease (ALS)

    MedlinePlus

    ... 1930s. People in England and Australia call ALS motor neurone disease (MND). The French refer to it ... about ALS in 1869. Lou Gehrig's disease damages motor neurons in the brain and spinal cord. Motor ...

  14. In situ visualisation and characterisation of the capacity of highly reactive minerals to preserve soil organic matter (SOM) in colloids at submicron scale.

    PubMed

    Xiao, Jian; Wen, Yongli; Li, Huan; Hao, Jialong; Shen, Qirong; Ran, Wei; Mei, Xinlan; He, Xinhua; Yu, Guanghui

    2015-11-01

    Mineral-organo associations (MOAs) are a mixture of identifiable biopolymers associated with highly reactive minerals and microorganisms. However, the in situ characterization and correlation between soil organic matter (SOM) and highly reactive Al and Fe minerals are still unclear for the lack of technologies, particularly in the long-term agricultural soil colloids at submicron scale. We combined several novel techniques, including nano-scale secondary ion mass spectrometry (NanoSIMS), X-ray absorption near edge structure (XANES) and confocal laser scanning microscopy (CLSM) to characterise the capacity of highly reactive Al and Fe minerals to preserve SOM in Ferralic Cambisol in south China. Our results demonstrated that: (1) highly reactive minerals were strongly related to SOM preservation, while SOM had a more significant line correlation with the highly reactive Al minerals than the highly reactive Fe minerals, according to the regions of interest correlation analyses using NanoSIMS; (2) allophane and ferrihydrite were the potential mineral species to determine the SOM preservation capability, which was evaluated by the X-ray photoelectron spectroscopy (XPS) and Fe K-edge XANES spectroscopy techniques; and (3) soil organic biopolymers with dominant compounds, such as proteins, polysaccharides and lipids, were distributed at the rough and clustered surface of MOAs with high chemical and spatial heterogeneity according to the CLSM observation. Our results also promoted the understanding of the roles played by the highly reactive Al and Fe minerals in the spatial distribution of soil organic biopolymers and SOM sequestration.

  15. Evaporites, petroleum and mineral resources

    SciTech Connect

    Melvin, J.L.

    1991-01-01

    This book illustrates the expanding knowledge of evaporites as important reservoir seals, fluid aquitards, ore-hosting sediments, and economically viable sediments in their own right. Researchers, oil and gas professionals, minerals resource professionals, environmental specialists and others within geology and the other earth sciences shall utilize the information within this book in their understanding of the many recent discoveries and concepts involved in the field of evaporite sedimentology.

  16. Mineral of the month: garnet

    USGS Publications Warehouse

    Olson, Donald

    2005-01-01

    Garnet is the general name given to a group of complex silicate minerals, all with isometric crystal structure, similar properties and chemical compositions. Garnet occurs in every color of the spectrum except blue, but it is most commonly red, purple, brown and green. Garnet necklaces dating from the Bronze Age have been found in graves and also among the ornaments adorning the oldest Egyptian mummies.

  17. Legionella pneumophila in coal miners.

    PubMed Central

    Davies, D H; Hill, E C; Howells, C H; Ribeiro, C D

    1985-01-01

    Legionnaires' disease was diagnosed in three mineworkers at a colliery. Investigation of water samples from various sites at the colliery did not discover a source of the infection. Results of serological surveys undertaken on the workmates of the patients and other miners showed only one additional positive Legionella indirect fluorescent antibody test. There was, therefore, no justification for any alteration in the water supply or the ventilation at the colliery. Images PMID:3890934

  18. Sequence of mineral assemblages in differentiated granitic pegmatites.

    USGS Publications Warehouse

    Norton, J.J.

    1983-01-01

    The sequence of mineral assemblages in internally zoned granitic pegmatites recognized by Cameron et al. (1949) is modified here to account for an observed vertical component, especially in feldspar compositions, in addition to the recognized outer contact-to-inner core differentiation process, and the importance of primary lithium minerals other than spodumene, such as petalite. The zonal patterns of 11 well-known granitic pegmatites are consistent with this revised sequence, with additional explanations for the repeated monomineralic zones of quartz or pollucite, etc. The crystallization history of zoned pegmatites is described in general terms, beginning with the magmatic crystallization which produces the outer zones. Aqueous fluid is exsolved continuously from the magma as relatively anhydrous phases precipitate, and plays an important role in the formation of the inner zones; its evolution is thought to be a major cause of pegmatite differentiation.-J.E.S.

  19. The Extraction of Altered Minerals by use of Hyperspectral and Aster Data and Their Comparison Research in Beketan, Altyn

    NASA Astrophysics Data System (ADS)

    Yi, H.; Li, J. Q.; Ren, G. L.; Yang, M.; Han, H. H.; Gao, T.; Yang, J. L.

    2016-11-01

    Hyperspectral remote sensing technology has played an important role in the field of geological application in recent years. Based on the reflectance of typical altered minerals and the spectral characteristics of rocks, we tried to identify and extract the altered minerals such as calcite, dolomite, epidote, chlorite, moscovite, limonite, hematite, etc. by using of CASI/SASI data in Beketan, Altyn. Moreover, we extracted Mg-OH/CO32-/Al-OH/Fe3+/Ferric oxide from Aster data by the ratio method. Combined with known geological background and the field investigation, we found that the extracted altered mineral information was consistent with the actual distribution of the field. The altered mineral information extracted by Hyperspectral data dispalyed more mineral distribution in details. It showed that the hyperspectral remote sensing technology could provide accurate hydrothermal altered mineral information which is helpful for geological mapping work.

  20. 36 CFR 331.17 - Minerals.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 36 Parks, Forests, and Public Property 3 2014-07-01 2014-07-01 false Minerals. 331.17 Section 331..., KENTUCKY AND INDIANA § 331.17 Minerals. All activities in connection with prospecting, exploration, development, mining or other removal or the processing of mineral resources and all uses reasonably...

  1. 36 CFR 331.17 - Minerals.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 36 Parks, Forests, and Public Property 3 2013-07-01 2012-07-01 true Minerals. 331.17 Section 331..., KENTUCKY AND INDIANA § 331.17 Minerals. All activities in connection with prospecting, exploration, development, mining or other removal or the processing of mineral resources and all uses reasonably...

  2. 36 CFR 331.17 - Minerals.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 36 Parks, Forests, and Public Property 3 2012-07-01 2012-07-01 false Minerals. 331.17 Section 331..., KENTUCKY AND INDIANA § 331.17 Minerals. All activities in connection with prospecting, exploration, development, mining or other removal or the processing of mineral resources and all uses reasonably...

  3. 36 CFR 331.17 - Minerals.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 36 Parks, Forests, and Public Property 3 2011-07-01 2011-07-01 false Minerals. 331.17 Section 331..., KENTUCKY AND INDIANA § 331.17 Minerals. All activities in connection with prospecting, exploration, development, mining or other removal or the processing of mineral resources and all uses reasonably...

  4. Raising Environmental Awareness among Miners in Iran

    ERIC Educational Resources Information Center

    Mozaffari, Ezatollah

    2013-01-01

    Generation of waste is inevitable but controllable in minerals industry. The aim of this research is to find ways for raising environmental awareness among miners. Miners' attitude towards environmental mining has been investigated. A survey has been done collecting mine managers' point of view coupled with current trend on mine waste management…

  5. Is Struvite a Prebiotic Mineral?

    PubMed Central

    Gull, Maheen; Pasek, Matthew A.

    2013-01-01

    The prebiotic relevance of mineral struvite, MgNH4PO4·6H2O, was studied experimentally as a phosphorylating reagent and, theoretically, to understand the geochemical requirements for its formation. The effectiveness of phosphorylation by the phosphate mineral, monetite, CaHPO4, was also studied to compare to the efficiency of struvite. The experiments focused on the phosphorylation reactions of the minerals with organic compounds, such as nucleosides, glycerol and choline chloride, and heat at 75 °C for about 7–8 days and showed up to 28% phosphorylation of glycerol. In contrast, the compositional requirements for the precipitation of struvite are high ammonium and phosphate concentrations, as well as a little Ca2+ dissolved in the water. Combined, these requirements suggest that it is not likely that struvite was present in excess on the early Earth to carry out phosphorylation reactions. The present study focuses on the thermodynamic aspects of struvite formation, complementing the results given by Orgel and Handschuh (1973), which were based on the kinetic effects. PMID:25369744

  6. Minerals

    MedlinePlus

    ... meat, such as beef tuna and salmon eggs beans baked potato with skins dried fruits, like raisins ... low-fat milk and yogurt legumes, such as beans, split peas, and lentils Zinc Zinc helps your ...

  7. Minerals

    MedlinePlus

    ... whole and enriched grains, like wheat or oats Potassium Potassium (say: puh-TAH-see-um) keeps your muscles ... system working properly. Which foods are rich in potassium? bananas tomatoes potatoes and sweet potatoes, with skins ...

  8. Minerals

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Over the past two decades, the aquaculture industry has expanded rapidly throughout the world and is expected to continue to grow in the years to come due to the high cost of harvesting fish from the oceans, the un-sustainability of ocean fishing methods, and the increased demand for fish as a resul...

  9. Characteristics of Hydrothermal Mineralization in Ultraslow Spreading Ridges

    NASA Astrophysics Data System (ADS)

    Zhou, H.; Yang, Q.; Ji, F.; Dick, H. J.

    2014-12-01

    Hydrothermal activity is a major component of the processes that shape the composition and structure of the ocean crust, providing a major pathway for the exchange of heat and elements between the Earth's crust and oceans, and a locus for intense biological activity on the seafloor and underlying crust. In other hand, the structure and composition of hydrothermal systems are the result of complex interactions between heat sources, fluids, wall rocks, tectonic controls and even biological processes. Ultraslow spreading ridges, including the Southwest Indian Ridge, the Gakkel Ridge, are most remarkable end member in plate-boundary structures (Dick et al., 2003), featured with extensive tectonic amagmatic spreading and frequent exposure of peridotite and gabbro. With intensive surveys in last decades, it is suggested that ultraslow ridges are several times more effective than faster-spreading ridges in sustaining hydrothermal activities. This increased efficiency could attributed to deep mining of heat and even exothermic serpentinisation (Baker et al., 2004). Distinct from in faster spreading ridges, one characteristics of hydrothermal mineralization on seafloor in ultraslow spreading ridges, including the active Dragon Flag hydrothermal field at 49.6 degree of the Southwest Indian Ridge, is abundant and pervasive distribution of lower temperature precipitated minerals ( such as Fe-silica or silica, Mn (Fe) oxides, sepiolite, pyrite, marcasite etc. ) in hydrothermal fields. Structures formed by lower temperature activities in active and dead hydrothermal fields are also obviously. High temperature precipitated minerals such as chalcopyrite etc. are rare or very limited in hydrothermal chimneys. Distribution of diverse low temperature hydrothermal activities is consistence with the deep heating mechanisms and hydrothermal circulations in the complex background of ultraslow spreading tectonics. Meanwhile, deeper and larger mineralization at certain locations along the

  10. 25 CFR 215.25 - Other minerals and deep-lying lead and zinc minerals.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 25 Indians 1 2013-04-01 2013-04-01 false Other minerals and deep-lying lead and zinc minerals. 215.25 Section 215.25 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR ENERGY AND MINERALS LEAD AND ZINC MINING OPERATIONS AND LEASES, QUAPAW AGENCY § 215.25 Other minerals and deep-lying...

  11. 25 CFR 215.25 - Other minerals and deep-lying lead and zinc minerals.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 25 Indians 1 2014-04-01 2014-04-01 false Other minerals and deep-lying lead and zinc minerals. 215.25 Section 215.25 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR ENERGY AND MINERALS LEAD AND ZINC MINING OPERATIONS AND LEASES, QUAPAW AGENCY § 215.25 Other minerals and deep-lying...

  12. 25 CFR 215.25 - Other minerals and deep-lying lead and zinc minerals.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 25 Indians 1 2012-04-01 2011-04-01 true Other minerals and deep-lying lead and zinc minerals. 215.25 Section 215.25 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR ENERGY AND MINERALS LEAD AND ZINC MINING OPERATIONS AND LEASES, QUAPAW AGENCY § 215.25 Other minerals and deep-lying...

  13. 25 CFR 215.25 - Other minerals and deep-lying lead and zinc minerals.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 25 Indians 1 2011-04-01 2011-04-01 false Other minerals and deep-lying lead and zinc minerals. 215.25 Section 215.25 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR ENERGY AND MINERALS LEAD AND ZINC MINING OPERATIONS AND LEASES, QUAPAW AGENCY § 215.25 Other minerals and deep-lying...

  14. 25 CFR 215.25 - Other minerals and deep-lying lead and zinc minerals.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 25 Indians 1 2010-04-01 2010-04-01 false Other minerals and deep-lying lead and zinc minerals. 215.25 Section 215.25 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR ENERGY AND MINERALS LEAD AND ZINC MINING OPERATIONS AND LEASES, QUAPAW AGENCY § 215.25 Other minerals and deep-lying...

  15. A detailed study of ice nucleation by feldspar minerals

    NASA Astrophysics Data System (ADS)

    Whale, T. F.; Murray, B. J.; Wilson, T. W.; Carpenter, M. A.; Harrison, A.; Holden, M. A.; Vergara Temprado, J.; Morris, J.; O'Sullivan, D.

    2015-12-01

    Immersion mode heterogeneous ice nucleation plays a crucial role in controlling the composition of mixed phase clouds, which contain both supercooled liquid water and ice particles. The amount of ice in mixed phase clouds can affect cloud particle size, lifetime and extent and so affects radiative properties and precipitation. Feldspar minerals are probably the most important minerals for ice nucleation in mixed phase clouds because they nucleate ice more efficiently than other components of atmospheric mineral dust (Atkinson et al. 2013). The feldspar class of minerals is complex, containing numerous chemical compositions, several crystal polymorphs and wide variations in microscopic structure. Here we present the results of a study into ice nucleation by a wide range of different feldspars. We found that, in general, alkali feldspars nucleate ice more efficiently than plagioclase feldspars. However, we also found that particular alkali feldspars nucleate ice relatively inefficiently, suggesting that chemical composition is not the only important factor that dictates the ice nucleation efficiency of feldspar minerals. Ice nucleation by feldspar is described well by the singular model and is probably site specific in nature. The alkali feldspars that do not nucleate ice efficiently possess relatively homogenous structure on the micrometre scale suggesting that the important sites for nucleation are related to surface topography. Ice nucleation active site densities for the majority of tested alkali feldspars are similar to those found by Atkinson et al (2013), meaning that the validity of global aerosol modelling conducted in that study is not affected. Additionally, we have found that ice nucleation by feldspars is strongly influenced, both positively and negatively, by the solute content of droplets. Most other nucleants we have tested are unaffected by solutes. This provides insight into the mechanism of ice nucleation by feldspars and could be of importance

  16. Mineral resource of the month: Vermiculite

    USGS Publications Warehouse

    Tanner, Arnold O.

    2014-01-01

    Vermiculite comprises a group of hydrated, laminar magnesium-aluminum-iron silicate minerals resembling mica. They are secondary minerals, typically altered biotite, iron-rich phlogopite or other micas or clay-like minerals that are themselves sometimes alteration products of amphibole, chlorite, olivine and pyroxene. Vermiculite deposits are associated with volcanic ultramafic rocks rich in magnesium silicate minerals, and flakes of the mineral range in color from black to shades of brown and yellow. The crystal structure of vermiculite contains water molecules, a property that is critical to its processing for common uses.

  17. Review of Distribution Coefficients for Radionuclides in Carbonate Minerals

    SciTech Connect

    Sutton, M

    2009-08-14

    An understanding of the transport of radionuclides in carbonate minerals is necessary to be able to predict the fate of (and potentially remediate) radionuclides in the environment. In some environments, carbonate minerals such as calciate, aragonite, dolomite and limestone are present and an understanding of the sorption of radionuclides in these carbonate minerals is therefore advantageous. A list of the radionuclides of interest is given in Table 1. The distribution coefficient, K{sub d} is defined as the ratio of the contaminant concentration bound on the solid phase to the contaminant concentration remaining in the liquid phase at equilibrium. Some authors report distribution coefficients and other report partition coefficients, the data presented in this work assumes equality between these two terms, and data are presented and summarized in this work as logarithmic distribution coefficient (log K{sub D}). Published literature was searched using two methods. Firstly, the JNC Sorption Database, namely Shubutani et al (1999), and Suyama and Sasamoto (2004) was used to select elements of interest and a number of carbonate minerals. Secondly, on-line literature search tools were used to locate relevant published articles from 1900 to 2009. Over 300 data points covering 16 elements (hydrogen, carbon, calcium, nickel, strontium, technetium, palladium, iodine, cesium, samarium, europium, holmium, uranium, neptunium, plutonium and americium) were used to calculate an average and range of log K{sub d} values for each element. Unfortunately, no data could be found for chlorine, argon, krypton, zirconium, niobium, tin, thorium and curium. A description of the data is given below, together with the average, standard deviation, minimum, maximum and number of inputs for radionuclide K{sub d} values for calcite, aragonate, limestone, dolomite and unidentified carbonate rocks in Table 2. Finally, the data are condensed into one group (carbonate minerals) of data for each

  18. The nanophase iron mineral(s) in Mars soil

    NASA Technical Reports Server (NTRS)

    Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Gehring, A. U.

    1992-01-01

    Iron-enriched smectites have been suggested as important mineral compounds of the Martian soil. They were shown to comply with the chemical analysis of the Martian soil, to simulate many of the findings of the Viking Labeled Release Experiments on Mars, to have spectral reflectance in the VIS-NIR strongly resembling the bright regions on Mars. The analogy with Mars soil is based, in a number of aspects, on the nature and behavior of the iron oxides and oxyhydroxides deposited on the surface of the clay particles. A summary of the properties of these iron phases and some recent findings are presented. Their potential relevance to Mars surface processes is discussed.

  19. Mineral and trace metal supplement for use with synthetic diets based on comminuted chicken.

    PubMed

    Thorn, J M; Aggett, P J; Delves, H T; Clayton, B E

    1978-12-01

    Earlier studies (Alexander et al., 1974; Lawson et al., 1977) suggested a suitable composition for a mineral and trace metal supplement for use with synthetic diets containing some natural food. Such a mixture has been evaluated in patients receiving a diet based on comminuted chicken and has been shown to be adequate. This conclusion was based on balance experiments measuring Zn, Cu, Mn, Fe, Ca, Mg, N, and P.

  20. TitaniQ recrystallized: experimental confirmation of the original Ti-in-quartz calibrations

    NASA Astrophysics Data System (ADS)

    Thomas, Jay B.; Watson, E. Bruce; Spear, Frank S.; Wark, D. A.

    2015-03-01

    Several studies have reported the P- T dependencies of Ti-in-quartz solubility, and there is close agreement among three of the four experimental calibrations. New experiments were conducted in the present study to identify potential experimental disequilibrium, and to determine which Ti-in-quartz solubility calibration is most accurate. Crystals of quartz, rutile and zircon were grown from SiO2-, TiO2-, and ZrSiO4-saturated aqueous fluids in an initial synthesis experiment at 925 °C and 10 kbar in a piston-cylinder apparatus. A range of quartz crystal sizes was produced in this experiment; both large and small examples were analyzed by electron microprobe to determine whether Ti concentrations are correlated with crystal size. Cathodoluminescence images and EPMA measurements show that intercrystalline and intracrystalline variations in Ti concentrations are remarkably small regardless of crystal size. The average Ti-in-quartz concentration from the synthesis experiment is 392 ± 1 ppmw Ti, which is within 95 % confidence interval of data from the 10 kbar isobar of Wark and Watson (Contrib Mineral Petrol 152:743-754, 2006) and Thomas et al. (Contrib Mineral Petrol 160:743-759, 2010). As a cross-check on the Ti-in-quartz calibration, we also measured the concentration of Zr in rutile from the synthesis experiment. The average Zr-in-rutile concentration is 4337 ± 32 ppmw Zr, which is also within the 95 % confidence interval of the Zr-in-rutile solubility calibration of Ferry and Watson (Contrib Mineral Petrol 154:429-437, 2007). The P- T dependencies of Ti solubility in quartz and Zr solubility in rutile were applied as a thermobarometer to the experimental sample. The average Ti-in-quartz isopleth calculated from the calibration of Thomas et al. (Contrib Mineral Petrol 160:743-759, 2010) and the average Zr-in-rutile isopleth calculated from the calibration of Tomkins et al. (J Metamorph Geol 25:703-713, 2007) cross at 9.5 kbar and 920 °C, which is in excellent

  1. Structure-mechanics relationships in mineralized tendons.

    PubMed

    Spiesz, Ewa M; Zysset, Philippe K

    2015-12-01

    In this paper, we review the hierarchical structure and the resulting elastic properties of mineralized tendons as obtained by various multiscale experimental and computational methods spanning from nano- to macroscale. The mechanical properties of mineralized collagen fibres are important to understand the mechanics of hard tissues constituted by complex arrangements of these fibres, like in human lamellar bone. The uniaxial mineralized collagen fibre array naturally occurring in avian tendons is a well studied model tissue for investigating various stages of tissue mineralization and the corresponding elastic properties. Some avian tendons mineralize with maturation, which results in a graded structure containing two zones of distinct morphology, circumferential and interstitial. These zones exhibit different amounts of mineral, collagen, pores and a different mineral distribution between collagen fibrillar and extrafibrillar space that lead to distinct elastic properties. Mineralized tendon cells have two phenotypes: elongated tenocytes placed between fibres in the circumferential zone and cuboidal cells with lower aspect ratios in the interstitial zone. Interestingly some regions of avian tendons seem to be predestined to mineralization, which is exhibited as specific collagen cross-linking patterns as well as distribution of minor tendon constituents (like proteoglycans) and loss of collagen crimp. Results of investigations in naturally mineralizing avian tendons may be useful in understanding the pathological mineralization occurring in some human tendons.

  2. Decorin modulates matrix mineralization in vitro

    NASA Technical Reports Server (NTRS)

    Mochida, Yoshiyuki; Duarte, Wagner R.; Tanzawa, Hideki; Paschalis, Eleftherios P.; Yamauchi, Mitsuo

    2003-01-01

    Decorin (DCN), a member of small leucine-rich proteoglycans, is known to modulate collagen fibrillogenesis. In order to investigate the potential roles of DCN in collagen matrix mineralization, several stable osteoblastic cell clones expressing higher (sense-DCN, S-DCN) and lower (antisense-DCN, As-DCN) levels of DCN were generated and the mineralized nodules formed by these clones were characterized. In comparison with control cells, the onset of mineralization by S-DCN clones was significantly delayed; whereas it was markedly accelerated and the number of mineralized nodules was significantly increased in As-DCN clones. The timing of mineralization was inversely correlated with the level of DCN synthesis. In these clones, the patterns of cell proliferation and differentiation appeared unaffected. These results suggest that DCN may act as an inhibitor of collagen matrix mineralization, thus modulating the timing of matrix mineralization.

  3. Mineralization of Carbon Dioxide: Literature Review

    SciTech Connect

    Romanov, V; Soong, Y; Carney, C; Rush, G; Nielsen, B; O'Connor, W

    2015-01-01

    CCS research has been focused on CO2 storage in geologic formations, with many potential risks. An alternative to conventional geologic storage is carbon mineralization, where CO2 is reacted with metal cations to form carbonate minerals. Mineralization methods can be broadly divided into two categories: in situ and ex situ. In situ mineralization, or mineral trapping, is a component of underground geologic sequestration, in which a portion of the injected CO2 reacts with alkaline rock present in the target formation to form solid carbonate species. In ex situ mineralization, the carbonation reaction occurs above ground, within a separate reactor or industrial process. This literature review is meant to provide an update on the current status of research on CO2 mineralization. 2

  4. Biofortifying crops with essential mineral elements.

    PubMed

    White, Philip J; Broadley, Martin R

    2005-12-01

    Humans require more than 22 mineral elements, which can all be supplied by an appropriate diet. However, the diets of populations subsisting on cereals, or inhabiting regions where soil mineral imbalances occur, often lack Fe, Zn, Ca, Mg, Cu, I or Se. Traditional strategies to deliver these minerals to susceptible populations have relied on supplementation or food fortification programs. Unfortunately, these interventions have not always been successful. An alternative solution is to increase mineral concentrations in edible crops. This is termed 'biofortification'. It can be achieved by mineral fertilization or plant breeding. There is considerable genetic variation in crop species that can be harnessed for sustainable biofortification strategies. Varieties with increased mineral concentrations in their edible portions are already available, and new genotypes with higher mineral densities are being developed.

  5. Multifaceted role of clay minerals in pharmaceuticals

    PubMed Central

    Khurana, Inderpreet Singh; Kaur, Satvinder; Kaur, Harpreet; Khurana, Rajneet Kaur

    2015-01-01

    The desirable physical and physiochemical properties of clay minerals have led them to play a substantial role in pharmaceutical formulations. Clay minerals like kaolin, smectite and palygorskite-sepiolite are among the world's most valuable industrial minerals and of considerable importance. The elemental features of clay minerals which caused them to be used in pharmaceutical formulations are high specific area, sorption capacity, favorable rheological properties, chemical inertness, swelling capacity, reactivity to acids and inconsiderable toxicity. Of course, these are highly cost effectual. This special report on clay minerals provides a bird's eye view of the chemical composition and structure of these minerals and their influence on the release properties of active medicinal agents. Endeavor has been made to rope in myriad applications depicting the wide acceptability of these clay minerals. PMID:28031881

  6. The Minerals of Aureum Chaos

    NASA Technical Reports Server (NTRS)

    2008-01-01

    [figure removed for brevity, see original site] Click on image for animation of 3-dimensional model with 5x vertical exaggeration

    This image of chaotic terrain in the Aureum Chaos region of Mars was taken by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) at 0858UTC (3:58 a.m. EST) on January 24, 2008, near 3.66 degrees south latitude, 26.5 degrees west longitude. The image was taken in 544 colors covering 0.36-3.92 micrometers, and shows features as small as 18 meters (60 feet) across. The image is about 10 kilometers (6.2 miles) wide at its narrowest point.

    Aureum Chaos is a 368 kilometer (229 mile) wide area of chaotic terrain in the eastern part of Valles Marineris. The chaotic terrain is thought to have formed by collapse of the surrounding Margaritifer Terra highland region. Aureum Chaos contains heavily eroded, randomly oriented mesas, plateaus, and knobs many revealing distinct layered deposits along their slopes. These deposits may be formed from remnants of the collapsed highlands, sand carried by Martian winds, dust or volcanic ash that settled out of the atmosphere, or sediments laid down on the floor of an ancient lake.

    The top panel in the montage above shows the location of the CRISM image on a mosaic taken by the Mars Odyssey spacecraft's Thermal Emission Imaging System (THEMIS). The CRISM data cover a narrow plateau near the edge of the chaotic terrain, that stretches across from the southwest to the northeast.

    The lower left image, an infrared false color image, reveals the plateau and several eroded knobs of varying sizes. The plateau's layer-cake structure is similar to that of other layered outcrops in Valles Marineris.

    The lower right image reveals the strengths of mineral spectral features overlain on a black-and-white version of the infrared image. Areas shaded in red hold more of the mineral pyroxene, a primary component of basaltic rocks that are prevalent in the highlands. Spots of green

  7. Origin of secondary sulfate minerals on active andesitic stratovolcanoes

    USGS Publications Warehouse

    Zimbelman, D.R.; Rye, R.O.; Breit, G.N.

    2005-01-01

    Sulfate minerals in altered rocks on the upper flanks and summits of active andesitic stratovolcanoes result from multiple processes. The origin of these sulfates at five active volcanoes, Citlalte??petl (Mexico), and Mount Adams, Hood, Rainier, and Shasta (Cascade Range, USA), was investigated using field observations, petrography, mineralogy, chemical modeling, and stable-isotope data. The four general groups of sulfate minerals identified are: (1) alunite group, (2) jarosite group, (3) readily soluble Fe- and Al-hydroxysulfates, and (4) simple alkaline-earth sulfates such as anhydrite, gypsum, and barite. Generalized assemblages of spatially associated secondary minerals were recognized: (1) alunite+silica??pyrite??kaolinite?? gypsum??sulfur, (2) jarosite+alunite+silica; (3) jarosite+smectite+silica??pyrite, (4) Fe- and Al-hydroxysulfates+silica, and (5) simple sulfates+silica??Al-hydroxysulfates??alunite. Isotopic data verify that all sulfate and sulfide minerals and their associated alteration assemblages result largely from the introduction of sulfur-bearing magmatic gases into meteoric water in the upper levels of the volcanoes. The sulfur and oxygen isotopic data for all minerals indicate the general mixing of aqueous sulfate derived from deep (largely disproportionation of SO2 in magmatic vapor) and shallow (oxidation of pyrite or H2S) sources. The hydrogen and oxygen isotopic data of alunite indicate the mixing of magmatic and meteoric fluids. Some alunite-group minerals, along with kaolinite, formed from sulfuric acid created by the disproportionation of SO2 in a condensing magmatic vapor. Such alunite, observed only in those volcanoes whose interiors are exposed by erosion or edifice collapse, may have ??34S values that reflect equilibrium (350??50 ??C) between aqueous sulfate and H2S. Alunite with ??34S values indicating disequilibrium between parent aqueous sulfate and H2S may form from aqueous sulfate created in higher level low

  8. Fungal biomineralization of montmorillonite and goethite to short-range-ordered minerals

    NASA Astrophysics Data System (ADS)

    Li, Huan; Hu, Shuijin; Polizzotto, Matthew L.; Chang, Xiaoli; Shen, Qirong; Ran, Wei; Yu, Guanghui

    2016-10-01

    Highly reactive nano-scale minerals, e.g., short-range-ordered minerals (SROs) and other nanoparticles, play an important role in soil carbon (C) retention. Yet, the mechanisms that govern biomineralization from bulk minerals to highly reactive nano-scale minerals remain largely unexplored, which critically hinders our efforts toward managing nano-scale minerals for soil C retention. Here we report the results from a study that explores structural changes during Aspergillus fumigatus Z5 transformation of montmorillonite and goethite to SROs. We examined the morphology and structure of nano-scale minerals, using high-resolution transmission electron microscopy, time-resolved solid-state 27Al and 29Si NMR, and Fe K-edge X-ray absorption fine structure spectroscopy combined with two dimensional correlation spectroscopy (2D COS) analysis. Our results showed that after a 48-h cultivation of montmorillonite and goethite with Z5, new biogenic intracellular and extracellular reactive nano-scale minerals with a size of 3-5 nm became abundant. Analysis of 2D COS further suggested that montmorillonite and goethite were the precursors of the dominant biogenic nano-scale minerals. Carbon 1s near edge X-ray absorption fine structure (NEXAFS) spectra and their deconvolution results demonstrated that during fungus Z5 growth, carboxylic C (288.4-289.1 eV) was the dominant organic group, accounting for approximately 34% and 59% in the medium and aggregates, respectively. This result suggested that high percentage of the production of organic acids during the growth of Z5 was the driving factor for structural changes during biomineralization. This is, to the best of our knowledge, the first report of the structural characterization of nano-scale minerals by 2D COS, highlighting its potential to elucidate biomineralization pathways and thus identify the precursors of nano-scale minerals.

  9. Mineral Influence on Microbial Survival During Carbon Sequestration

    NASA Astrophysics Data System (ADS)

    Santillan, E. U.; Shanahan, T. M.; Wolfe, W. W.; Bennett, P.

    2012-12-01

    CO2 sequestered in a deep saline aquifer will perturb subsurface biogeochemistry by acidifying the groundwater and accelerating mineral diagenesis. Subsurface microbial communities heavily influence geochemistry through their metabolic processes, such as with dissimilatory iron reducing bacteria (DIRB). However, CO2 also acts as a sterilant and will perturb these communities. We investigated the role of mineralogy and its effect on the survival of microbes at high PCO2 conditions using the model DIRB Shewanella oneidensis MR-1. Batch cultures of Shewanella were grown to stationary phase and exposed to high PCO2 using modified Parr reactors. Cell viability was then determined by plating cultures after exposure. Results indicate that at low PCO2 (2 bar), growth and iron reduction are decreased and cell death occurs within 1 hour when exposed to CO2 pressures of 10 bar or greater. Further, fatty acid analysis indicates microbial lipid degradation with C18 fatty acids being the slowest lipids to degrade. When cultures were grown in the presence of rocks or minerals representative of the deep subsurface such as carbonates and silicates and exposed to 25 bar CO2, survival lasted beyond 2 hours. The most effective protecting substratum was quartz sandstone, with cultures surviving beyond 8 hours of CO2 exposure. Scanning electron microscope images reveal biofilm formation on the mineral surfaces with copious amounts of extracellular polymeric substances (EPS) present. EPS from these biofilms acts as a reactive barrier to the CO2, slowing the penetration of CO2 into cells and resulting in increased survival. When biofilm cultures were grown with Al and As to simulate the release of toxic metals from minerals such as feldspars and clays, survival time decreased, indicating mineralogy may also enhance microbial death. Biofilms were then grown on iron-coated quartz sand to determine conversely what influence biofilms may have on mineral dissolution during CO2 perturbation

  10. Evaluating biodiversity of mineral lands

    SciTech Connect

    Wade, G.L.; Tritton, L.M.

    1997-12-31

    Increasingly, lands intended for mining, or lands that have been mined and reclaimed, are being evaluated in terms of biological diversity (biodiversity). The concept of biodiversity includes die variety and number of living organisms, their organizations, and the environments that support them. This paper presents a framework for discussing and evaluating biodiversity and for constructing checklists for evaluating biodiversity before and after mining. This framework identifies some of the different types of biodiversity applicable to mineral lands, die ranges of scale at which they are applicable, and the social stakes and stakeholders relevant across scale and diversity types.

  11. Draft Genome Sequence of Ensifer adhaerens M78, a Mineral-Weathering Bacterium Isolated from Soil

    PubMed Central

    Wang, Yuanli; Chen, Wei; He, Linyan; Wang, Qi

    2016-01-01

    Ensifer adhaerens M78, a bacterium isolated from soil, can weather potash feldspar and release Fe, Si, and Al from rock under nutrient-poor conditions. Here, we report the draft genome sequence of strain M78, which may facilitate a better understanding of the molecular mechanism involved in mineral weathering by the bacterium. PMID:27609930

  12. Draft Genome Sequence of Ensifer adhaerens M78, a Mineral-Weathering Bacterium Isolated from Soil.

    PubMed

    Wang, Yuanli; Chen, Wei; He, Linyan; Wang, Qi; Sheng, Xia-Fang

    2016-09-08

    Ensifer adhaerens M78, a bacterium isolated from soil, can weather potash feldspar and release Fe, Si, and Al from rock under nutrient-poor conditions. Here, we report the draft genome sequence of strain M78, which may facilitate a better understanding of the molecular mechanism involved in mineral weathering by the bacterium.

  13. Luna 20 - Mineral chemistry of spinel, pleonaste, chromite, ulvospinel, ilmenite and rutile.

    NASA Technical Reports Server (NTRS)

    Haggerty, S. E.

    1973-01-01

    Review of some of the results of a reflection microscopy and electron microprobe study performed on a part of the Luna 20 soil sample designated as the East Coast Consortium aliquot. The study is restricted to analyses of the oxides of Fe, Ti, Mg, Mn, Cr, and Al in this sample. The spinel mineral group, ilmenite and rutile only are discussed.

  14. Inclusions of crichtonite group minerals in pyropes from the Internatsionalnaya kimberlite pipe, Yakutia

    NASA Astrophysics Data System (ADS)

    Rezvukhin, D. I.; Malkovets, V. G.; Sharygin, I. S.; Kuzmin, D. V.; Gibsher, A. A.; Litasov, K. D.; Pokhilenko, N. P.; Sobolev, N. V.

    2016-02-01

    The results of study of crichtonite group minerals in pyropes from the Internatsionalnaya kimberlite pipe are reported. Most of the studied samples are characterized by high concentrations of Sr, Ca, Na, and LREEs in comparison with minerals of the LIMA series from kimberlites of South Africa, whereas the average concentrations of Ba and K are significantly lower. Crichtonite group minerals in pyropes are characterized by predomination of Na over K in most samples and by a high concentration of Al2O3 (up to 4.5 wt %). Findings of inclusions of crichtonite group minerals with high concentrations of incompatible elements provide evidence for the metasomatic origin of host chromium-rich pyropes.

  15. Structure and chemical characteristics of natural mineral deposit Terbunskaya (Lipetsk region, Russia)

    NASA Astrophysics Data System (ADS)

    Motyleva, S.; Shchuchka, R.; Gulidova, V.; Mertvishcheva, M.

    2015-07-01

    New knowledge about the mineralogical features Terbunsky mineral. Investigated 5 fractions isolated from the incision (2-2,5 m). Terbunskaya deposit belongs to minerals Santonian age. Scanning electron microscopy and energy dispersive analysis of fractions isolated studied in detail. In the coarse fractions found ancient organic remains of algae and micro-organisms that have been sedimented together with the mineral component during geological periods. The share of organic inclusions does not exceed 1.5%. Chemical composition confirms the presence of silicon and carbonate organisms. Advantageously proportion of minerals having a layered structure with a plurality of micro and nano pore size 600 - 80-nm and an average chemical composition (wt%): Na (0,64), Mg (0,54), Al (13.48), Si (27 57), K (2.39) Ca (0.75).

  16. Physiology of bone: Mineral compartment proteins as candidates for environmental perturbation by lead

    SciTech Connect

    Sauk, J.J.; Somerman, M.J. )

    1991-02-01

    Termine et al. first demonstrated that sequential dissociative extraction and fractionation procedures with protease inhibitors could provide a convenient approach for the study of mineral compartment constituents. The primary extraction regimen used 4 M guanidine HCl to remove most of the protein from the nonmineralized phase of bone. Subsequently, EDTA-guanidine was used to remove the mineral-phase components. These methods discriminate on the basis of physical-chemical association with a mineral phase rather than on the specific gene products of a particular cell. In the present discussion emphasis is directed at a group of divalent cation binding proteins isolated from the mineral compartment of bone. The localization, synthesis, and chemical characteristics of osteonectin, bone sialoproteins I and II, and bone acidic glycoprotein-75 are discussed and offered as possible sites for perturbation by the environment with lead exposure.

  17. Structure and chemical characteristics of natural mineral deposit Terbunskaya (Lipetsk region, Russia)

    SciTech Connect

    Motyleva, S. Mertvishcheva, M.; Shchuchka, R.; Gulidova, V.

    2015-07-22

    New knowledge about the mineralogical features Terbunsky mineral. Investigated 5 fractions isolated from the incision (2-2,5 m). Terbunskaya deposit belongs to minerals Santonian age. Scanning electron microscopy and energy dispersive analysis of fractions isolated studied in detail. In the coarse fractions found ancient organic remains of algae and micro-organisms that have been sedimented together with the mineral component during geological periods. The share of organic inclusions does not exceed 1.5%. Chemical composition confirms the presence of silicon and carbonate organisms. Advantageously proportion of minerals having a layered structure with a plurality of micro and nano pore size 600 - 80-nm and an average chemical composition (wt%): Na (0,64), Mg (0,54), Al (13.48), Si (27 57), K (2.39) Ca (0.75)

  18. Determination of minerals extracted from several commercial teas (Camellia sinensis) to hot water (infusion).

    PubMed

    Gezgin, Sait; Ozcan, Mehmet Musa; Atalay, Emine

    2006-01-01

    Mineral contents of some tea and their infusions drunk in Turkey were established by inductively coupled plasma atomic emission spectrometry. The Al, Ca, K, Mg, Mn, P, and S contents were very high in both infusions and tea (i.e., pieces of the tea plant). The As, Cd, Cr, Li, Pb, and Se contents of infusion and tea were found to be very low. The level of K of all samples is higher than those of other minerals. Generally, mineral contents of tea were found to be higher than those of tea infusions. In addition, the health benefits of teas and knowledge of their mineral contents are of great interest and may be useful for further study of enzyme systems and vital biochemical functions.

  19. Physiology of bone: mineral compartment proteins as candidates for environmental perturbation by lead.

    PubMed Central

    Sauk, J J; Somerman, M J

    1991-01-01

    Termine et al. first demonstrated that sequential dissociative extraction and fractionation procedures with protease inhibitors could provide a convenient approach for the study of mineral compartment constituents. The primary extraction regimen used 4 M guanidine HCl to remove most of the protein from the nonmineralized phase of bone. Subsequently, EDTA-guanidine was used to remove the mineral-phase components. These methods discriminate on the basis of physical-chemical association with a mineral phase rather than on the specific gene products of a particular cell. In the present discussion emphasis is directed at a group of divalent cation binding proteins isolated from the mineral compartment of bone. The localization, synthesis, and chemical characteristics of osteonectin, bone sialoproteins I and II, and bone acidic glycoprotein-75 are discussed and offered as possible sites for perturbation by the environment with lead exposure. Images FIGURE 1. FIGURE 2. FIGURE 2. FIGURE 2. FIGURE 3. FIGURE 3. FIGURE 3. FIGURE 3. PMID:2040255

  20. A Film Depositional Model of Permeability for Mineral Reactions in Unsaturated Media.

    SciTech Connect

    Freedman, Vicky L.; Saripalli, Prasad; Bacon, Diana H.; Meyer, Philip D.

    2004-11-15

    A new modeling approach based on the biofilm models of Taylor et al. (1990, Water Resources Research, 26, 2153-2159) has been developed for modeling changes in porosity and permeability in saturated porous media and implemented in an inorganic reactive transport code. Application of the film depositional models to mineral precipitation and dissolution reactions requires that calculations of mineral films be dynamically changing as a function of time dependent reaction processes. Since calculations of film thicknesses do not consider mineral density, results show that the film porosity model does not adequately describe volumetric changes in the porous medium. These effects can be included in permeability calculations by coupling the film permeability models (Mualem and Childs and Collis-George) to a volumetric model that incorporates both mineral density and reactive surface area. Model simulations demonstrate that an important difference between the biofilm and mineral film models is in the translation of changes in mineral radii to changes in pore space. Including the effect of tortuosity on pore radii changes improves the performance of the Mualem permeability model for both precipitation and dissolution. Results from simulation of simultaneous dissolution and secondary mineral precipitation provides reasonable estimates of porosity and permeability. Moreover, a comparison of experimental and simulated data show that the model yields qualitatively reasonable results for permeability changes due to solid-aqueous phase reactions.

  1. 30 CFR 281.8 - Rights to minerals.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false Rights to minerals. 281.8 Section 281.8 Mineral Resources MINERALS MANAGEMENT SERVICE, DEPARTMENT OF THE INTERIOR OFFSHORE LEASING OF MINERALS OTHER THAN OIL, GAS, AND SULPHUR IN THE OUTER CONTINENTAL SHELF General § 281.8 Rights to minerals. (a)...

  2. Mineral Resource Information System for Field Lab in the Osage Mineral Reservation Estate

    SciTech Connect

    Carroll, H.B.; Johnson, William I.

    1999-04-27

    The Osage Mineral Reservation Estate is located in Osage County, Oklahoma. Minerals on the Estate are owned by members of the Osage Tribe who are shareholders in the Estate. The Estate is administered by the Osage Agency, Branch of Minerals, operated by the U.S. Bureau of Indian Affairs (BIA). Oil, natural gas, casinghead gas, and other minerals (sand, gravel, limestone, and dolomite) are exploited by lessors. Operators may obtain from the Branch of Minerals and the Osage Mineral Estate Tribal Council leases to explore and exploit oil, gas, oil and gas, and other minerals on the Estate. Operators pay a royalty on all minerals exploited and sold from the Estate. A mineral Resource Information system was developed for this project to evaluate the remaining hydrocarbon resources located on the Estate. Databases on Microsoft Excel spreadsheets of operators, leases, and production were designed for use in conjunction with an evaluation spreadsheet for estimating the remaining hydrocarbons on the Estate.

  3. H4 and H5 chondrites from the Rub'al Khali desert

    NASA Astrophysics Data System (ADS)

    Krot, A. N.

    1993-06-01

    Based on texture and mineral composition, the highly weathered al-Jimshan chondrite is classed as an S2-shock stage H4 chondrite. The Bir-Hadi and ad-Dahbubah H chondrites are probably not paired with al-Jimshan, and are here respectively classified as H5, shock stage S3 and H5, shock stage S2.

  4. H4 and H5 chondrites from the Rub'al Khali desert

    NASA Technical Reports Server (NTRS)

    Krot, Aleksandr N.

    1993-01-01

    Based on texture and mineral composition, the highly weathered al-Jimshan chondrite is classed as an S2-shock stage H4 chondrite. The Bir-Hadi and ad-Dahbubah H chondrites are probably not paired with al-Jimshan, and are here respectively classified as H5, shock stage S3 and H5, shock stage S2.

  5. Geostatistical Analysis of Spatial Variability of Mineral Abundance and Kd in Frenchman Flat, NTS, Alluvium

    SciTech Connect

    Carle, S F; Zavarin, M; Pawloski, G A

    2002-11-01

    LLNL hydrologic source term modeling at the Cambric site (Pawloski et al., 2000) showed that retardation of radionuclide transport is sensitive to the distribution and amount of radionuclide sorbing minerals. While all mineralogic information available near the Cambric site was used in these early simulations (11 mineral abundance analyses from UE-5n and 9 from RNM-l), these older data sets were qualitative in nature, with detection limits too high to accurately measure many of the important radionuclide sorbing minerals (e.g. iron oxide). Also, the sparse nature of the mineral abundance data permitted only a hypothetical description of the spatial distribution of radionuclide sorbing minerals. Yet, the modeling results predicted that the spatial distribution of sorbing minerals would strongly affect radionuclide transport. Clearly, additional data are needed to improve understanding of mineral abundances and their spatial distributions if model predictions in Frenchman Flat are to be defensible. This report evaluates new high-resolution quantitative X-Ray Diffraction (XRD) data on mineral distributions and their abundances from core samples recently collected from drill hole ER-5-4. The total of 94 samples from ER-5-4 were collected at various spacings to enable evaluation of spatial variability at a variety of spatial scales as small as 0.3 meters and up to hundreds of meters. Additional XRD analyses obtained from drillholes UE-Sn, ER-5-3, and U-11g-1 are used to augment evaluation of vertical spatial variability and permit some evaluation of lateral spatial variability. A total of 163 samples are evaluated. The overall goal of this study is to understand and characterize the spatial variation of sorbing minerals in Frenchman Flat alluvium using geostatistical techniques, with consideration for the potential impact on reactive transport of radionuclides. To achieve this goal requires an effort to ensure that plausible geostatistical models are used to

  6. Constraints on the Mineral Evolution of Terrestrial Planets Using Statistical Correlations Among the Mineral-Forming Elements

    NASA Astrophysics Data System (ADS)

    Hummer, D. R.; Hazen, R. M.; Golden, J.; Downs, R. T.

    2015-12-01

    The mineralogy of terrestrial planets is governed not only by size, bulk chemical composition, planetary differentiation processes, and secondary geochemical processes, but also by the fundamental way in which a planet's constituent elements parse themselves into mineral species. To gain insight into which elements tend to associate with each other to form minerals, we have used the IMA mineralogical database (rruff.info/ima) to conduct a statistical analysis of the number of known mineral species containing each of the 72 mineral-forming elements, as well as how many species contain both X and Y for every possible X-Y pair of elements. The frequency with which elements X and Y occur together in the nominal chemical formulae of minerals was compared with the expected rate of co-occurrence (assuming that elements are distributed among mineral species randomly). The results reveal that among the most strongly correlated element pairs are H-O, Na-Si, Al-Si, S-Ag, O-Si, Si-Ca, and O-Ca. Examples of strongly anti-correlated pairs are O-S, O-Ag, Si-S, O-Sb, O-Se, H-Ag, and Si-As. The strength of these correlations and anti-correlations varied by many orders of magnitude (as measured by their p-value in a chi-squared test for variable dependence), ranging from near 1 to an astounding 10-304. Out of 2520 unique element pairs, 1688 were statistically significant (p-value <0.05). These pair correlations can be attributed to an array of geochemical factors, including but not limited to 1) the mutual exclusivity of sulfide vs. silicate anionic groups, 2) crystal chemical considerations of size and charge similarities among cations, especially within silicate structures, 3) group relationships on the periodic table, and 4) soft vs. hard ion relationships. These principles, along with the specific correlations they produce, can serve as a valuable guide in explaining the mineral evolution of Earth's crust, and predicting the mineralogy of terrestrial planets even when the bulk

  7. Analysis of aquifer mineralization by paleodrainage channels

    USGS Publications Warehouse

    Rubin, H.; Buddemeier, R.W.

    2003-01-01

    Mineralization of groundwater resources is a problem in south-central Kansas, due to the penetration of saline water from Permian bedrock formations into the overlying alluvial aquifer. One of the mechanisms involved in the mineralization involves small bedrock features of high permeability located in places occupied by streams and rivers in past geological eras. These geological features are termed 'paleodrainage channels'. The permeability of the overlying aquifer can be significantly smaller than that of the channel fill material. The comparatively fast migration of saline water through these channels of high permeability is associated with the transfer of minerals into the overlying freshwater aquifer. This study applies a set of boundary layer approaches to quantify the process of mineral transfer from the channels into the aquifer. The methods used in the present study provide quick estimation and evaluation of the dilution of the channel flow, as well as mineral concentration profile changes in the mineralized zone created in the overlying aquifer. More generally, the method can also be useful for the analysis and evaluation of various types of groundwater contamination in heterogeneous aquifers. The application of the method is exemplified by a complete set of calculations characterizing the possible mineralization process at a specific channel in south central Kansas. Sensitivity analyses are performed and provide information about the importance of the various parameters that affect the mineralization process. Some possible scenarios for the aquifer mineralization phenomena are described and evaluated. It is shown that the channel mineralization may create either several stream tubes of the aquifer with high mineral concentration, or many stream tubes mineralized to a lesser extent. Characteristics of these two patterns of aquifer mineralization are quantified and discussed. ?? 2003 Published by Elsevier Science B.V.

  8. Minerals, fibrosis, and the lung.

    PubMed Central

    Heppleston, A G

    1991-01-01

    Determinants of pulmonary fibrosis induced by inhaled mineral dusts include quantity retained, particle size, and surface area, together with their physical form and the reactive surface groups presented to alveolar cells. The outstanding problem is to ascertain how these factors exert their deleterious effects. Both compact and fibrous minerals inflict membrane damage, for which chemical mechanisms still leave uncertainty. A major weakness of cytotoxicity studies, even when lipid peroxidation and reactive oxygen species are considered, lies in tacitly assuming that membrane damage suffices to account for fibrogenesis, whereas the parallel occurrence of such manifestations does not necessarily imply causation. The two-phase procedure established that particles, both compact and fibrous, induce release of a macrophage factor that provokes fibroblasts into collagen synthesis. The amino acid composition of the macrophage fibrogenic factor was characterized and its intracellular action explained. Fibrous particles introduce complexities respecting type, durability, and dimensions. Asbestotic fibrosis is believed to depend on long fibers, but scrutiny of the evidence from experimental and human sources reveals that a role for short fibers needs to be entertained. Using the two-phase system, short fibers proved fibrogenic. Other mechanisms, agonistic and antagonistic, may participate. Growth factors may affect the fibroblast population and collagen production, with cytokines such as interleukin-1 and tumor necrosis factor exerting control. Immune involvement is best regarded as an epiphenomenon. Downregulation of fibrogenesis may follow collagenase release from macrophages and fibroblasts, while augmented type II cell secretion of lipid can interfere with the macrophage-particle reaction. PMID:1954926

  9. Mineral Resources Data System (MRDS)

    USGS Publications Warehouse

    Mason, G.T.; Arndt, R.E.

    1996-01-01

    The U.S. Geological Survey (USGS) operates the Mineral Resources Data System (MRDS), a digital system that contained 111,955 records on Sept. 1, 1995. Records describe metallic and industrial commodity deposits, mines, prospects, and occurrences in the United States and selected other countries. These records have been created over the years by USGS commodity specialists and through cooperative agreements with geological surveys of U.S. States and other countries. This CD-ROM contains the complete MRDS data base, several subsets of it, and software to allow data retrieval and display. Data retrievals are made by using GSSEARCH, a program that is included on this CD-ROM. Retrievals are made by specifying fields or any combination of the fields that provide information on deposit name, location, commodity, deposit model type, geology, mineral production, reserves, and references. A tutorial is included. Retrieved records may be printed or written to a hard disk file in four different formats: ascii, fixed, comma delimited, and DBASE compatible.

  10. Raman Spectroscopy of Mineral Inclusions in Diamonds from Yakutia

    NASA Astrophysics Data System (ADS)

    Ugap'eva, Sargylana; Goryainov, Sergey; Afanasiev, Valentine

    2016-10-01

    New data on the study of residual pressure in mineral inclusions in diamonds from kimberlite pipes and placers of Yakutia obtained using Raman Spectroscopy are presented. Calculated values of residual pressure in olivine and coesite inclusions in kimberlite diamonds according to works of Israeli et al [1] and Sobolev et al [2] indicate that the host crystal crystallized at the depth not less than 165 km, at pressure of 4.8-5.0 GPa and temperature T=1200 °C. Comparative analysis of Raman spectra of olivine inclusions in diamonds from placers of Ebelyakh river on inclusions, contained in diamond and then brought to the surface, showed that olivine inclusions are less stressed. The structural orientation of olivine inclusions in diamonds from placers of Ebelyakh river possibly plays a role in these differences of Raman spectra.

  11. Pacific subduction and Mesozoic mineralization in eastern China

    NASA Astrophysics Data System (ADS)

    Sun, W.; Ling, M.; Liang, H.; Ding, X.; Fan, W.; Yang, X.

    2009-12-01

    Northeastern China is well known for the removal of subcontinental lithosphere mantle of the North China craton in the Late Mesozoic and the Cretaceous giant igneous event, while southeastern China is famous for its large scale magmatism and mineralization from the Late Jurassic to the Early Cretaceous. All these can be plausibly interpreted by the interaction between eastern China and the subducting Pacific plate. From Jurassic to Cretaceous, Eastern China was related to the subduction of the Pacific plate under Eurasia in the south, concurrent with oblique subduction of the Izanagi plate in the north (Maruyama et al., 1997; Li and Li, 2007; Sun et al., 2007; Zhou et al., 2000). Cretaceous tectonic evolution of eastern China matches remarkably well with the drifting history of the Pacific plate. The most pronounced phenomena are: (1) eastern China large-scale orogenic lode gold (Au) mineralisation occurred contemporaneously with an abrupt change of ~80 degree in the drifting direction of the subducting Pacific plate, concurrent with the formation of the Ontong Java Plateau (Sun et al., 2007); (2) the subduction of the ridge between the Pacific and Izanagi Plates can plausibly explain the mineralization and rock distribution of the Lower Yangtze River mineralization belt (Ling et al., 2009); (3) southwestward subduction of the Pacific plate and corresponding slab rollback can feasibly interprete the formation of the late Mesozoic (180-125 Ma) magmatism and metallogenic events in SE China. Reference Li, Z. X., and Li, X. H., 2007, Formation of the 1300-km-wide intracontinental orogen and postorogenic magmatic province in Mesozoic South China: A flat-slab subduction model: Geology, v. 35, p. 179-182. Ling, M. X., Wang, F. Y., Ding, X., Hu, Y. H., Zhou, J. B., Zartman, R. E., Yang, X. Y., and Sun, W. D., 2009, Cretaceous ridge subduction along the Lower Yangtze River Belt, eastern China: Economic Geology, v. 104, p. 303-321. Maruyama, S., 1997, Pacific-type orogeny

  12. Chemistry and mineralogy of clay minerals in Asian and Saharan dusts and the implications for iron availability

    NASA Astrophysics Data System (ADS)

    Jeong, G. Y.; Achterberg, E. P.

    2014-06-01

    Mineral dust supplied to remote ocean regions stimulates phytoplankton growth through delivery of micronutrients, notably iron (Fe). Although attention is usually paid to Fe (hydr)oxides as major sources of available Fe, Fe-bearing clay minerals are typically the dominant phase in mineral dust. The mineralogy and chemistry of clay minerals in dust particles, however, are largely unknown. We conducted microscopic identification and chemical analysis of the clay minerals in Asian and Saharan dust particles. Cross-sectional slices of dust particles were prepared by focused ion beam (FIB) techniques and analyzed by transmission electron microscopy (TEM) combined with energy dispersive X-ray spectroscopy (EDXS). TEM images of FIB slices revealed that clay minerals occurred as either nano-thin platelets or relatively thick plates. The nano-thin platelets included illite, smectite, illite-smectite mixed layers and their nanoscale mixtures (illite-smectite series clay minerals, ISCMs) which could not be resolved with an electron microbeam. EDXS chemical analysis of the clay mineral grains revealed that the average Fe content was 5.8% in nano-thin ISCM platelets assuming 14% H2O, while the Fe content of illite and chlorite was 2.8 and 14.8%, respectively. In addition, TEM and EDXS analyses were performed on clay mineral grains dispersed and loaded on microgrids. The average Fe content of clay mineral grains was 6.7 and 5.4% in Asian and Saharan dusts, respectively. A comparative X-ray diffraction analysis of bulk dusts showed that Saharan dust was more enriched in clay minerals than in Asian dust, while Asian dust was more enriched in chlorite. The average Fe / Si, Al / Si and Fe / Al molar ratios of the clay minerals, compared to previously reported chemistries of mineral dusts and leached solutions, indicated that dissolved Fe originated from clay minerals. Clay minerals, in particular nanocrystalline ISCMs and Fe-rich chlorite are important sources of available Fe in

  13. The nanosphere iron mineral(s) in Mars soil

    NASA Technical Reports Server (NTRS)

    Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Mancinelli, R. L.; Gehring, A. U.

    1993-01-01

    A series of surface-modified clays containing nanophase (np) iron/oxyhydroxides of extremely small particle sizes, with total iron contents as high as found in Mars soil, were prepared by iron deposition on the clay surface from ferrous chloride solution. Comprehensive studies of the iron mineralogy in these 'Mars-soil analogs' were conducted using chemical extractions, solubility analyses, pH and redox, x ray and electron diffractometry, electron microscopic imaging specific surface area and particle size determinations, differential thermal analyses, magnetic properties characterization, spectral reflectance, and Viking biology simulation experiments. The clay matrix and the procedure used for synthesis produced nanophase iron oxides containing a certain proportion of divalent iron, which slowly converts to more stable, fully oxidized iron minerals. The noncrystalline nature of the iron compounds precipitated on the surface of the clay was verified by their complete extractability in oxalate. Lepidocrocite (gamma-FeOOH) was detected by selected area electron diffraction. It is formed from a double iron Fe(II)/Fe(III) hydroxyl mineral such as 'green rust', or ferrosic hydroxide. Magnetic measurements suggested that lepidocrocite converted to the more stable meaghemite (gamma-Fe203) by mild heat treatment and then to nanophase hematite (aplha-Fe203) by extensive heat treatment. Their chemical reactivity offers a plausible mechanism for the somewhat puzzling observations of the Viking biology experiments. Their unique chemical reactivities are attributed to the combined catalytic effects of the iron oxide/oxyhydroxide and silicate phase surfaces. The mode of formation of these (nanophase) iron oxides on Mars is still unknown.

  14. The nanosphere iron mineral(s) in Mars soil

    NASA Astrophysics Data System (ADS)

    Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Mancinelli, R. L.; Gehring, A. U.

    1993-11-01

    A series of surface-modified clays containing nanophase (np) iron/oxyhydroxides of extremely small particle sizes, with total iron contents as high as found in Mars soil, were prepared by iron deposition on the clay surface from ferrous chloride solution. Comprehensive studies of the iron mineralogy in these 'Mars-soil analogs' were conducted using chemical extractions, solubility analyses, pH and redox, x ray and electron diffractometry, electron microscopic imaging specific surface area and particle size determinations, differential thermal analyses, magnetic properties characterization, spectral reflectance, and Viking biology simulation experiments. The clay matrix and the procedure used for synthesis produced nanophase iron oxides containing a certain proportion of divalent iron, which slowly converts to more stable, fully oxidized iron minerals. The noncrystalline nature of the iron compounds precipitated on the surface of the clay was verified by their complete extractability in oxalate. Lepidocrocite (gamma-FeOOH) was detected by selected area electron diffraction. It is formed from a double iron Fe(II)/Fe(III) hydroxyl mineral such as 'green rust', or ferrosic hydroxide. Magnetic measurements suggested that lepidocrocite converted to the more stable meaghemite (gamma-Fe203) by mild heat treatment and then to nanophase hematite (aplha-Fe203) by extensive heat treatment. Their chemical reactivity offers a plausible mechanism for the somewhat puzzling observations of the Viking biology experiments. Their unique chemical reactivities are attributed to the combined catalytic effects of the iron oxide/oxyhydroxide and silicate phase surfaces. The mode of formation of these (nanophase) iron oxides on Mars is still unknown.

  15. Soapstone (steatite) cookware as a source of minerals.

    PubMed

    Quintaes, K D; Amaya-Farfan, J; Morgano, M A; Mantovani, D M B

    2002-02-01

    Steatite or soapstone, is a soft metamorphic rock composed mainly of talc, dolomite and actinolite, which is abundantly found and used for the manufacture of cookware in south-east Brazil. The study estimates its usage for cookware among dwellers of Ouro Preto, and assesses the possible toxicological or nutritional impact on food preparation. Pans made of steatite were purchased both in the crude (n = 6) and 'cured'forms (n = 6). Migration of Ca, Fe, Mg, Mn, Co, Al, Cr, Ni, Pb and Cd was determined for 20 sequential cooking trials, using 3 and 5% acetic acid as a food simulant. Analytical determinations were carried out by inductively coupled plasma atomic-emission spectrometry and the data treated by an individual model of random effects, simple linear regression and Pearson's correlation. About 81% of Ouro Preto's native population own soapstone cookware and, of these, 79% use the pans regularly. Mineral migration followed the general solubility of the crystalline components of the rock. Therefore, Ca, Mg, Fe and Mn were, in that order, the elements that exhibited highest migration, whereas the remaining were seen in negligible levels, except for Ni in the crude pans. The 5% solution favoured migration, whereas curing tended to restrict migration and extend durability of the pan. It is concluded that while cured soapstone pans do not offer mineral toxicity, they may contribute to the mineral nutrition of human beings.

  16. Contributions to Industrial-Minerals Research

    USGS Publications Warehouse

    Bliss, James D.; Moyle, Phillip R.; Long, Keith R.

    2003-01-01

    Contributions to Industrial-Minerals Research, an ongoing series of U.S. Geological Survey (USGS) Bulletin chapters, presents research strategies, results, and updates of investigations of industrial minerals by USGS scientists and cooperators. Industrial minerals are defined as valuable nonmetallic, nonfuel geologic materials, generally rocks or minerals, used in a wide range of construction and industrial applications-for example, sand, gravel, and crushed rock used as aggregate for construction; limestone used for cement; phosphate for fertilizers and insecticides; and diatomite used for filtration, fillers, and abrasives. The term also comprises some processed materials, such as cement and metallic compounds with major utilization in nonmetallic forms. For example, titanium is commonly grouped with industrial minerals because more than 90 percent of it is sold and utilized in the form of the oxide (TiO2) rather than as Ti metal. Other metals and metallic compounds commonly grouped with industrial minerals include Mn, Cr, Fe oxides, and rare-earth elements (REEs).

  17. Regulation of bone mineral loss during lactation

    NASA Technical Reports Server (NTRS)

    Brommage, R.; Deluca, H. F.

    1985-01-01

    The effects of varyng dietary calcium and phosphorous levels, vitamin D deficiency, oophorectomy, adrenalectomy, and simultaneous pregnancy on bone mineral loss during lactation in rats are studied. The experimental procedures and evaluations are described. The femur ash weight of lactating and nonlactating rats are calculated. The data reveals that a decrease in dietary calcium of 0.02 percent results in an increased loss of bone mineral, an increase in calcium to 1.4 percent does not lessen bone mineral loss, and bone mineral loss in vitamin D deficient rats is independent of calcium levels. It is observed that changes in dietary phosphorous level, oophorectomy, adrenalectomy, and simultaneous pragnancy do not reduce bone mineral loss during lactation. The analysis of various hormones to determine the mechanism that triggers bone mineral loss during lactation is presented.

  18. Mortality from stomach cancer in Ontario miners.

    PubMed Central

    Kusiak, R A; Ritchie, A C; Springer, J; Muller, J

    1993-01-01

    An excess of mortality from stomach cancer has been found in Ontario gold miners (observed (obs) 104, standardised mortality ratio (SMR) 152, 95% confidence interval (95% CI) 125-185) and no excess of stomach cancer could be detected in other miners in Ontario (obs 74, SMR 102, 95% CI 80-128). The excess of stomach cancer appeared five to 19 years after the miners began gold mining in Ontario. In that interval, similar patterns of excess mortality from stomach cancer were found in miners born in north America (obs 14, SMR 268, CI 147-450) and in miners born outside north America (obs 12, SMR 280, 95% CI 145-489). Twenty or more years after the miners began mining gold, an excess of mortality from stomach cancer was found in gold miners born outside of north American (obs 41, SMR 160, 95% CI 115-218) but not in gold miners born in north America (obs 37, SMR 113, 95% CI 80-156). The excess of stomach cancer in gold miners under the age of 60 (obs 45, SMR 167, 95% CI 122-223) seems larger than the excess in gold miners between the ages of 60 and 74 (obs 59, SMR 143, 95% CI 109-184). Exposures to arsenic, chromium, mineral fibre, diesel emissions, and aluminium powder were considered as possible explanations of the excess of stomach cancer in Ontario gold miners. Exposure to diesel emissions and aluminium powder was rejected as gold miners and uranium miners were exposed to both agents but an excess of stomach cancer was noted only in gold miners. The association between the excess of stomach cancer and the time since the miner began mining gold suggested that duration of exposure to dust in gold mines ought to be weighted according to the time since the exposure to dust occurred and that an appropriate time weighting function would be one in the interval five to 19 years after each year of exposure to dust and zero otherwise. A statistically significant association between the relative risk of mortality from stomach cancer and the time weighted duration of exposure to

  19. Mineralization related to Alvand pluton in the Hamadan, western Iran

    NASA Astrophysics Data System (ADS)

    Salehi, M. H.; Doosti, E. A.; Ahadnejad, V.

    2009-04-01

    The Alvand (Hamadan) plutonic batholith is one of the largest plutonic bodies in the Sanandaj-Sirjan metamorphic belt. This complex is consist of mafic part (gabbro-diorite-tonalite), intermediate (granite-granodiorite porphyroids), and hololeucocratic granitoids. Previous studies have shown that S-type granite-granodiorites are mostly peraluminous and calc-alkaline; the gabbro-diorite-tonalite suite is mostly metaluminous and tholeiitic to calc-alkaline (Sepahi, 2008). High initial 87Sr-86Sr ratios (0.7081 to 0.7115), low epsilon Nd values (-1.0 to -3.3), and peraluminous character reflects a different origin for the granites, possibly crustal sources (Ghalamghash et al, 2007). Aplite-pegmatite dikes are intruded in granitoide rocks, metamorphic rocks and the contact of Alvand granite with metamorphic rocks. The contact of Alvand granite with metamorphic rocks is sharp. By using heavy mineral studies on the alluvium of Alvand complex, it is recognized 28 minerals amongst Scheelite, Cassiterite, Ilmenite, Zircon and Garnet. Different geostatistical studies such as variant, bivariant and multivariant studies have been done on rough data of heavy minerals. They showed normal concentration of gold in studied rocks and low enrichment of tin and tungsten. The index of the ore elements average, frequeney distribution criteria of elements, the ratio of elements index and multielements show that Alvand granite is barren. Mineralography studies did not recognized any tin and tungsten minerals. The grains of gold was recognized in some of the microscopic thin sections. Calcopyrotite is the most important ore mineral that is accompanied with oxides and iron carbonates. The contacts of aplite-pegmatite dikes with granitoide rocks mostly are not prolific. For recognizing Scheelite, some samples of rocks studied by ultraviolet and few Scheelite is recognized in the samples. Some alteration zone observed in this area but they are not accompany with main mineralization. Although

  20. Geochemical constraints on the presence of clay minerals in the Burns formation, Meridiani Planum, Mars

    NASA Astrophysics Data System (ADS)

    Cino, C. D.; Dehouck, E.; McLennan, S. M.

    2017-01-01

    Burns formation sandstones, deposited by aeolian processes and preserved at Meridiani Planum, Mars, contain abundant sulfate minerals. These sedimentary rocks are thought to be representative of a sulfate-rich geological epoch during late Noachian - early Hesperian time that followed an earlier clay-rich epoch. Twenty Burns formation targets, abraded by the Rock Abrasion Tool (RAT) and for which alpha-particle X-ray spectrometry (APXS) and Mössbauer spectroscopy data are available, were selected for geochemical modeling. A linear unmixing modeling approach was employed. Mineralogical constituents quantitatively constrained by Mössbauer and Mini-TES spectroscopy and interpreted to be chemically precipitated from aqueous fluids during deposition and/or early diagenesis were subtracted from the bulk chemistry. Resulting residual chemical compositions, interpreted to be dominated by detrital siliciclastic components and representing ∼21-35% of the rocks, were then geochemically evaluated to constrain the potential for the presence of clay minerals or their poorly-crystalline or non-crystalline precursors/chemical equivalents. Calculations incorporated a robust estimate of the uncertainties in mineral abundances. On Al2O3 - (CaO+Na2O) - K2O (A-CN-K) and Al2O3 - (CaO+Na2O+K2O) - (FeOtotal+MgO) (A-CNK-FM) molar ternary diagrams, removal of chemical constituents resulted in a shift from igneous-like compositions to compositions consistent with secondary mineral assemblages containing significant aluminous clay mineral components. All of the residual compositions are corundum-normative, further supportive of the presence of highly aluminous phases. On the A-CNK-FM diagram, clay minerals plotting closest to the residual field are natural montmorillonites but could also represent mixtures of various Mg/Fe-rich phyllosilicates, such as nontronite or saponite, and other more Al-rich minerals such as Al-montmorillonite, kaolinite or illite. Depending on the age of clay

  1. Hydrothermal Mineral-Assisted Organic Transformations of Carboxylic Acids

    NASA Astrophysics Data System (ADS)

    Johnson, K. N.; Gould, I.; Williams, L. B.; Hartnett, H. E.; Shock, E.

    2014-12-01

    The purpose of our research is to probe the varieties of reactions possible in a hydrothermal system in which both organic compounds and minerals interact. We performed experiments at physical conditions representative of deep-sea and subsurface systems (300°C and 1000 bar) and analyzed the effect of the mineral magnetite (Fe3O4) in systems with carboxylic acids, either phenylacetic acid or hydrocinnamic acid (a.k.a., phenylpropanoic acid). Control experiments were also conducted with the same organic compounds in the absence of magnetite. Whereas previous studies of carboxylic acid reactivity with minerals have focused exclusively on simple molecules such as acetic acid and valeric acid (Bell et al. 1994; McCollom et al. 2003), the carboxylic acids used in our study differ from previous experimental compounds by the addition of a phenyl ring, which allows for the investigation of the specific mechanistic pathways of product formation. Decarboxylation (i.e., RCO2H → RH + CO2) is one of the major reaction pathways for carboxylic acids in hydrothermal conditions without minerals. Under our experimental conditions, decarboxylation leads to the ~80% conversion of phenylacetic acid into toluene within ~50 hours and the ~8% conversion of hydrocinnamic acid to ethyl benzene within ~190 hours. We found that magnetite had a different effect on the two organic compounds studied. In experiments with phenylacetic acid, the presence of magnetite did not enhance the rate of toluene production from decarboxylation but did activate additional product pathways that include diphenyl alkanes, alkenes, and ketones, as well as benzoic acid, a carboxylic acid one carbon length shorter than the parent compound. Magnetite had even more noticeable effects on the hydrocinnamic acid system leading to an increase of its consumption at 190 hours from ~9% in magnetite's absence to ~35% in the mineral's presence. Products of the experiments with magnetite included an enhanced rate of

  2. Mineral Distributions at the Developing Tendon Enthesis

    PubMed Central

    Schwartz, Andrea G.; Pasteris, Jill D.; Genin, Guy M.; Daulton, Tyrone L.; Thomopoulos, Stavros

    2012-01-01

    Tendon attaches to bone across a functionally graded interface, “the enthesis”. A gradient of mineral content is believed to play an important role for dissipation of stress concentrations at mature fibrocartilaginous interfaces. Surgical repair of injured tendon to bone often fails, suggesting that the enthesis does not regenerate in a healing setting. Understanding the development and the micro/nano-meter structure of this unique interface may provide novel insights for the improvement of repair strategies. This study monitored the development of transitional tissue at the murine supraspinatus tendon enthesis, which begins postnatally and is completed by postnatal day 28. The micrometer-scale distribution of mineral across the developing enthesis was studied by X-ray micro-computed tomography and Raman microprobe spectroscopy. Analyzed regions were identified and further studied by histomorphometry. The nanometer-scale distribution of mineral and collagen fibrils at the developing interface was studied using transmission electron microscopy (TEM). A zone (∼20 µm) exhibiting a gradient in mineral relative to collagen was detected at the leading edge of the hard-soft tissue interface as early as postnatal day 7. Nanocharacterization by TEM suggested that this mineral gradient arose from intrinsic surface roughness on the scale of tens of nanometers at the mineralized front. Microcomputed tomography measurements indicated increases in bone mineral density with time. Raman spectroscopy measurements revealed that the mineral-to-collagen ratio on the mineralized side of the interface was constant throughout postnatal development. An increase in the carbonate concentration of the apatite mineral phase over time suggested possible matrix remodeling during postnatal development. Comparison of Raman-based observations of localized mineral content with histomorphological features indicated that development of the graded mineralized interface is linked to endochondral

  3. Mineral distributions at the developing tendon enthesis.

    PubMed

    Schwartz, Andrea G; Pasteris, Jill D; Genin, Guy M; Daulton, Tyrone L; Thomopoulos, Stavros

    2012-01-01

    Tendon attaches to bone across a functionally graded interface, "the enthesis". A gradient of mineral content is believed to play an important role for dissipation of stress concentrations at mature fibrocartilaginous interfaces. Surgical repair of injured tendon to bone often fails, suggesting that the enthesis does not regenerate in a healing setting. Understanding the development and the micro/nano-meter structure of this unique interface may provide novel insights for the improvement of repair strategies. This study monitored the development of transitional tissue at the murine supraspinatus tendon enthesis, which begins postnatally and is completed by postnatal day 28. The micrometer-scale distribution of mineral across the developing enthesis was studied by X-ray micro-computed tomography and Raman microprobe spectroscopy. Analyzed regions were identified and further studied by histomorphometry. The nanometer-scale distribution of mineral and collagen fibrils at the developing interface was studied using transmission electron microscopy (TEM). A zone (∼20 µm) exhibiting a gradient in mineral relative to collagen was detected at the leading edge of the hard-soft tissue interface as early as postnatal day 7. Nanocharacterization by TEM suggested that this mineral gradient arose from intrinsic surface roughness on the scale of tens of nanometers at the mineralized front. Microcomputed tomography measurements indicated increases in bone mineral density with time. Raman spectroscopy measurements revealed that the mineral-to-collagen ratio on the mineralized side of the interface was constant throughout postnatal development. An increase in the carbonate concentration of the apatite mineral phase over time suggested possible matrix remodeling during postnatal development. Comparison of Raman-based observations of localized mineral content with histomorphological features indicated that development of the graded mineralized interface is linked to endochondral

  4. Mineral resource of the month: Mica

    USGS Publications Warehouse

    Willett, Jason C.

    2014-01-01

    The mica mineral group includes 34 phyllosilicate minerals, all with a layered, platy texture. The mineral has been known for millennia: Mica was first mined in India about 4,000 years ago, where it was used primarily in medicines. The Mayans used it for decorative effect in stucco to make their temples sparkle in the sun. Today it is used in everything from electrical products to makeup.

  5. Correlation of ameloblastin with enamel mineral content

    PubMed Central

    Teepe, John D.; Schmitz, James E.; Hu, Yuanyuan; Yamada, Yoshihiko; Fajardo, Roberto J.; Smith, Charles E.; Chun, Yong-Hee P.

    2015-01-01

    In enamel formation, the deposition of minerals as crystallites starts when the mineralization front first forms at the start of the secretory stage. During maturation, the enamel layer accumulates significant amounts of new mineral as the crystallites grow in volume. Inversely related to mineral gain is loss of protein and water from the forming enamel. Both ameloblastin (Ambn) and enamelin are essential components for formation of a functional enamel layer. The aim of this study was to quantify the proportion of mineral and non-mineral material present in developing enamel relative to Ambn concentration using Ambn mutant mice mated with others overexpressing full-length Ambn from the mouse amelogenin promoter at lower (+), similar (++) or higher (+++) concentration than normal. Mandibular incisors (age: 7 weeks, n=8) were imaged by micro-computed tomography and the enamel was analyzed from the apical region to the incisal edge in sequential 1.0 mm volumes of interest. Mineral density was determined using a series of hydroxyapatite (HA) phantoms to calibrate enamel density measurements. At the site where the mandibular incisor emerged into the oral cavity, the enamel volume, mineral weight, and mineral density were reduced when Tg Ambn was expressed at lower or higher levels than normal. While in wild-type the % mineral was >95%, it was negligible in Ambn−/−, 22.3% in Ambn−/−, Tg(+), 75.4% in Ambn−/−, Tg(++), and 45.2% in Ambn−/−, Tg(+++). These results document that the deposition of mineral and removal of non-mineral components are both very sensitive to expressed Ambn concentrations. PMID:25158178

  6. The role of reaction affinity and secondary minerals in regulating chemical weathering rates at the Santa Cruz Soil Chronosequence, California

    SciTech Connect

    Maher, K.; Steefel, C. I.; White, A.F.; Stonestrom, D.A.

    2009-02-25

    In order to explore the reasons for the apparent discrepancy between laboratory and field weathering rates and to determine the extent to which weathering rates are controlled by the approach to thermodynamic equilibrium, secondary mineral precipitation and flow rates, a multicomponent reactive transport model (CrunchFlow) was used to interpret soil profile development and mineral precipitation and dissolution rates at the 226 ka marine terrace chronosequence near Santa Cruz, CA. Aqueous compositions, fluid chemistry, transport, and mineral abundances are well characterized (White et al., 2008, GCA) and were used to constrain the reaction rates for the weathering and precipitating minerals in the reactive transport modeling. When primary mineral weathering rates are calculated with either of two experimentally determined rate constants, the nonlinear, parallel rate law formulation of Hellmann and Tisser and [2006] or the aluminum inhibition model proposed by Oelkers et al. [1994], modeling results are consistent with field-scale observations when independently constrained clay precipitation rates are accounted for. Experimental and field rates, therefore, can be reconciled at the Santa Cruz site. Observed maximum clay abundances in the argillic horizons occur at the depth and time where the reaction fronts of the primary minerals overlap. The modeling indicates that the argillic horizon at Santa Cruz can be explained almost entirely by weathering of primary minerals and in situ clay precipitation accompanied by undersaturation of kaolinite at the top of the profile. The rate constant for kaolinite precipitation was also determined based on model simulations of mineral abundances and dissolved Al, SiO{sub 2}(aq) and pH in pore waters. Changes in the rate of kaolinite precipitation or the flow rate do not affect the gradient of the primary mineral weathering profiles, but instead control the rate of propagation of the primary mineral weathering fronts and thus total

  7. Genetic testing in ALS

    PubMed Central

    McLaughlin, Russell L.; Heverin, Mark; Thorpe, Owen; Abrahams, Sharon; Al-Chalabi, Ammar; Hardiman, Orla

    2017-01-01

    Objective: To determine the degree of consensus among clinicians on the clinical use of genetic testing in amyotrophic lateral sclerosis (ALS) and the factors that determine decision-making. Methods: ALS researchers worldwide were invited to participate in a detailed online survey to determine their attitudes and practices relating to genetic testing. Results: Responses from 167 clinicians from 21 different countries were analyzed. The majority of respondents (73.3%) do not consider that there is a consensus definition of familial ALS (FALS). Fifty-seven percent consider a family history of frontotemporal dementia and 48.5% the presence of a known ALS genetic mutation as sufficient for a diagnosis of FALS. Most respondents (90.2%) offer genetic testing to patients they define as having FALS and 49.4% to patients with sporadic ALS. Four main genes (SOD1, C9orf72, TARDBP, and FUS) are commonly tested. A total of 55.2% of respondents would seek genetic testing if they had personally received a diagnosis of ALS. Forty-two percent never offer presymptomatic testing to family members of patients with FALS. Responses varied between ALS specialists and nonspecialists and based on the number of new patients seen per year. Conclusions: There is a lack of consensus among clinicians as to the definition of FALS. Substantial variation exists in attitude and practices related to genetic testing of patients and presymptomatic testing of their relatives across geographic regions and between experienced specialists in ALS and nonspecialists. PMID:28159885

  8. Interaction of root exudates with the mineral soil constituents and their effect on mineral weathering

    NASA Astrophysics Data System (ADS)

    Mimmo, T.; Terzano, R.; Medici, L.; Lettino, A.; Fiore, S.; Tomasi, N.; Pinton, R.; Cesco, S.

    2012-04-01

    Plants release significant amounts of high and low molecular weight organic compounds into the rhizosphere. Among these exudates organic acids (e.g. citric acid, malic acid, oxalic acid), phenolic compounds (e.g. flavonoids), amino acids and siderophores of microbial and/or plant origin strongly influence and modify the biogeochemical cycles of several elements, thus causing changes in their availability for plant nutrition. One class of these elements is composed by the trace elements; some of them are essential for plants even if in small concentrations and are considered micronutrients, such as Fe, Zn, Mn. Their solubility and bioavailability can be influenced, among other factors, by the presence in soil solution of low molecular weight root exudates acting as organic complexing agents that can contribute to the mineral weathering and therefore, to their mobilization in the soil solution. The mobilized elements, in function of the element and of its concentration, can be either important nutrients or toxic elements for plants. The objective of this study was to assess the influence of several root exudates (citric acid, malic acid, oxalic acid, genistein, quercetin and siderophores) on the mineralogy of two different soils (an agricultural calcareous soil and an acidic polluted soil) and to evaluate possible synergic or competitive behaviors. X-ray diffraction (XRD) coupled with Electron Probe Micro Analysis (EPMA) was used to identify the crystalline and amorphous phases which were subjected to mineral alteration when exposed to the action of root exudates. Solubilization of trace metals such as Cu, Zn, Ni, Cr, Pb, Cd as well as of major elements such as Si, Al, Fe and Mn was assessed by means of Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). Soil microorganisms have proven to decrease mineral weathering by reducing the concentration of active root exudates in solution. Results obtained are an important cornerstone to better understand the

  9. Multiphase Sequestration Geochemistry: Model for Mineral Carbonation

    SciTech Connect

    White, Mark D.; McGrail, B. Peter; Schaef, Herbert T.; Hu, Jian Z.; Hoyt, David W.; Felmy, Andrew R.; Rosso, Kevin M.; Wurstner, Signe K.

    2011-04-01

    Carbonation of formation minerals converts low viscosity supercritical CO2 injected into deep saline reservoirs for geologic sequestration into an immobile form. Until recently the scientific focus of mineralization reactions with reservoir rocks has been those that follow an aqueous-mediated dissolution/precipitation mechanism, driven by the sharp reduction in pH that occurs with CO2 partitioning into the aqueous phase. For sedimentary basin formations the kinetics of aqueous-mediated dissolution/precipitation reactions are sufficiently slow to make the role of mineralization trapping insignificant over a century period. For basaltic saline formations aqueous-phase mineralization progresses at a substantially higher rate, making the role of mineralization trapping significant, if not dominant, over a century period. The overlooked mineralization reactions for both sedimentary and basaltic saline formations, however, are those that occur in liquid or supercritical CO2 phase; where, dissolved water appears to play a catalyst role in the formation of carbonate minerals. A model is proposed in this paper that describes mineral carbonation over sequestration reservoir conditions ranging from dissolved CO2 in aqueous brine to dissolved water in supercritical CO2. The model theory is based on a review of recent experiments directed at understanding the role of water in mineral carbonation reactions of interest in geologic sequestration systems occurring under low water contents.

  10. Mineral-Based Amendments for Remediation

    PubMed Central

    O’Day, Peggy A.; Vlassopoulos, Dimitri

    2011-01-01

    Amending soils with mineral-based materials to immobilize contaminants is both old and new. Although mineral amendments have been used for decades in agriculture, new applications with a variety of natural and reprocessed materials are emerging. By sequestering contaminants in or on solid phases and reducing their ability to partition into water or air, amendments can reduce the risk of exposure to humans or biota. A variety of mineral types are commonly used to amend contaminated soils, with different modes of molecular-scale sequestration. Regulatory, social, and economic factors also influence decisions to employ mineral amendments as a treatment technology. PMID:22203887

  11. Minerals yearbook, 1992: Louisiana. Annual report

    SciTech Connect

    White, D.H.; Marsalis, W.E.

    1994-03-01

    Louisiana's nonfuel mineral production in 1992 totaled $309.3 million. This was a $42.5 million decline in value from that reported by the mineral industry in 1991. Although there was an increase in the value of gemstones, lime, and industrial sand and gravel, it failed to offset a decline in the demand and sales of gypsum, construction sand and gravel, salt, crushed stone, and sulfur. The values of these five mineral commodities fell $53.9 million between 1991 and 1992. The State ranked 32d nationally in mineral value and accounted for 35% of the Nation's salt tonnage and 42% of the Frasch sulfur production.

  12. MINER: software for phylogenetic motif identification.

    PubMed

    La, David; Livesay, Dennis R

    2005-07-01

    MINER is web-based software for phylogenetic motif (PM) identification. PMs are sequence regions (fragments) that conserve the overall familial phylogeny. PMs have been shown to correspond to a wide variety of catalytic regions, substrate-binding sites and protein interfaces, making them ideal functional site predictions. The MINER output provides an intuitive interface for interactive PM sequence analysis and structural visualization. The web implementation of MINER is freely available at http://www.pmap.csupomona.edu/MINER/. Source code is available to the academic community on request.

  13. Mineral Facilities of Latin America and Canada

    USGS Publications Warehouse

    Bernstein, Rachel; Eros, Mike; Quintana-Velazquez, Meliany

    2006-01-01

    This data set consists of records for over 900 mineral facilities in Latin America and Canada. The mineral facilities include mines, plants, smelters, or refineries of aluminum, cement, coal, copper, diamond, gold, iron and steel, nickel, platinum-group metals, salt, and silver, among others. Records include attributes such as commodity, country, location, company name, facility type and capacity if applicable, and generalized coordinates. The data were compiled from multiple sources, including the 2003 and 2004 USGS Minerals Yearbooks (Latin America and Candada volume), data to be published in the 2005 Minerals Yearbook Latin America and Canada Volume, minerals statistics and information from the USGS minerals information Web site (minerals.usgs.gov/minerals), and data collected by USGS minerals information country specialists. Data reflect the most recent published table of industry structure for each country. Other sources include statistical publications of individual countries, annual reports and press releases of operating companies,and trade journals. Due to the sensitivity of some energy commodity data, the quality of these data should be evaluated on a country-by-country basis. Additional information and explanation is available from the country specialists.

  14. Plasmid-mediated mineralization of 4-chlorobiphenyl.

    PubMed Central

    Shields, M S; Hooper, S W; Sayler, G S

    1985-01-01

    Strains of Alcaligenes and Acinetobacter spp. were isolated from a mixed culture already proven to be proficient at complete mineralization of monohalogenated biphenyls. These strains were shown to harbor a 35 X 10(6)-dalton plasmid mediating a complete pathway for 4-chlorobiphenyl (4CB) oxidation. Subsequent plasmid curing of these bacteria resulted in the abolishment of the 4CB mineralization phenotype and loss of even early 4CB metabolism by Acinetobacter spp. Reestablishment of the Alcaligenes plasmid, denoted pSS50, in the cured Acinetobacter spp. via filter surface mating resulted in the restoration of 4CB mineralization abilities. 4CB mineralization, however, proved to be an unstable characteristic in some subcultured strains. Such loss was not found to coincide with any detectable alteration in plasmid size. Cultures capable of complete mineralization, as well as those limited to partial metabolism of 4CB, produced 4-chlorobenzoate as a metabolite. Demonstration of mineralization of a purified 14C-labeled chlorobenzoate showed it to be a true intermediate in 4CB mineralization. Unlike the mineralization capability, the ability to produce a metabolite has proven to be stable on subculture. These results indicate the occurrence of a novel plasmid, or evolved catabolic plasmid, that mediates the complete mineralization of 4CB. Images PMID:2993249

  15. TUCS/phosphate mineralization of actinides

    SciTech Connect

    Nash, K.L.

    1997-10-01

    This program has as its objective the development of a new technology that combines cation exchange and mineralization to reduce the concentration of heavy metals (in particular actinides) in groundwaters. The treatment regimen must be compatible with the groundwater and soil, potentially using groundwater/soil components to aid in the immobilization process. The delivery system (probably a water-soluble chelating agent) should first concentrate the radionuclides then release the precipitating anion, which forms thermodynamically stable mineral phases, either with the target metal ions alone or in combination with matrix cations. This approach should generate thermodynamically stable mineral phases resistant to weathering. The chelating agent should decompose spontaneously with time, release the mineralizing agent, and leave a residue that does not interfere with mineral formation. For the actinides, the ideal compound probably will release phosphate, as actinide phosphate mineral phases are among the least soluble species for these metals. The most promising means of delivering the precipitant would be to use a water-soluble, hydrolytically unstable complexant that functions in the initial stages as a cation exchanger to concentrate the metal ions. As it decomposes, the chelating agent releases phosphate to foster formation of crystalline mineral phases. Because it involves only the application of inexpensive reagents, the method of phosphate mineralization promises to be an economical alternative for in situ immobilization of radionuclides (actinides in particular). The method relies on the inherent (thermodynamic) stability of actinide mineral phases.

  16. Minerals yearbook, 1990: Massachusetts. Annual report

    SciTech Connect

    Harrison, D.K.; Sinnott, J.A.

    1992-09-01

    The value of nonfuel mineral production in 1990 was $127.5 million, a decrease of $16.6 million compared with the 1989 value. The combined value of crushed stone and construction sand and gravel, the State's two leading mineral commodities, accounted for 83% of the value. In 1990, the State ranked eighth among 34 States that produced dimension stone. Other commodities produced included common clay, industrial sand, lime, and peat. Industrial minerals processed or manufactured in the State included abrasives, graphite, gypsum, perlite, and vermiculite. The report presents statistical information on the state's mineral industries.

  17. Mineral resources, environmental issues, and land use.

    PubMed

    Hodges, C A

    1995-06-02

    Contrary to predictions from the 1950s through the mid-1980s, persistent shortages of nonfuel minerals have not occurred, despite prodigious consumption, and world reserves have increased. Global availability of raw materials is relevant to policy decisions regarding mineral development and land use. Justification for environmental protection may exceed that for mining a specific ore body. Demand for environmental accountability is rising worldwide, and new technologies are enabling internalization of costs. Mineral-rich developing nations plagued by inefficient state-owned mining enterprises, high population growth rates, and environmental degradation could realize substantial benefit by reforming government policies to encourage foreign investment in resources and by appropriate allocation of mineral rents.

  18. Citrate bridges between mineral platelets in bone.

    PubMed

    Davies, Erika; Müller, Karin H; Wong, Wai Ching; Pickard, Chris J; Reid, David G; Skepper, Jeremy N; Duer, Melinda J

    2014-04-08

    We provide evidence that citrate anions bridge between mineral platelets in bone and hypothesize that their presence acts to maintain separate platelets with disordered regions between them rather than gradual transformations into larger, more ordered blocks of mineral. To assess this hypothesis, we take as a model for a citrate bridging between layers of calcium phosphate mineral a double salt octacalcium phosphate citrate (OCP-citrate). We use a combination of multinuclear solid-state NMR spectroscopy, powder X-ray diffraction, and first principles electronic structure calculations to propose a quantitative structure for this material, in which citrate anions reside in a hydrated layer, bridging between apatitic layers. To assess the relevance of such a structure in native bone mineral, we present for the first time, to our knowledge, (17)O NMR data on bone and compare them with (17)O NMR data for OCP-citrate and other calcium phosphate minerals relevant to bone. The proposed structural model that we deduce from this work for bone mineral is a layered structure with thin apatitic platelets sandwiched between OCP-citrate-like hydrated layers. Such a structure can explain a number of known structural features of bone mineral: the thin, plate-like morphology of mature bone mineral crystals, the presence of significant quantities of strongly bound water molecules, and the relatively high concentration of hydrogen phosphate as well as the maintenance of a disordered region between mineral platelets.

  19. Dietary Supplements and Sports Performance: Minerals

    PubMed Central

    Williams, Melvin H

    2005-01-01

    Minerals are essential for a wide variety of metabolic and physiologic processes in the human body. Some of the physiologic roles of minerals important to athletes are their involvement in: muscle contraction, normal hearth rhythm, nerve impulse conduction, oxygen transport, oxidative phosphorylation, enzyme activation, immune functions, antioxidant activity, bone health, and acid-base balance of the blood. The two major classes of minerals are the macrominerals and the trace elements. The scope of this article will focus on the ergogenic theory and the efficacy of such mineral supplementation. PMID:18500950

  20. Dietary supplements and sports performance: minerals.

    PubMed

    Williams, Melvin H

    2005-06-11

    Minerals are essential for a wide variety of metabolic and physiologic processes in the human body. Some of the physiologic roles of minerals important to athletes are their involvement in: muscle contraction, normal hearth rhythm, nerve impulse conduction, oxygen transport, oxidative phosphorylation, enzyme activation, immune functions, antioxidant activity, bone health, and acid-base balance of the blood. The two major classes of minerals are the macrominerals and the trace elements. The scope of this article will focus on the ergogenic theory and the efficacy of such mineral supplementation.

  1. High concentration of residual aluminum oxide on titanium surface inhibits extracellular matrix mineralization.

    PubMed

    Canabarro, A; Diniz, M G; Paciornik, S; Carvalho, L; Sampaio, E M; Beloti, M M; Rosa, A L; Fischer, R G

    2008-12-01

    In the present study we characterized titanium (Ti) surfaces submitted to different treatments and evaluated the response of osteoblasts derived from human alveolar bone to these surfaces. Five different surfaces were evaluated: ground (G), ground and chemical etched (G1-HF for 60 s), sand blasted (SB-Al(2)O(3) particles 65 mum), sand blasted and chemical etched (SLA1-HF for 60 s and SLA2-HF for 13 s). Surface morphology was evaluated under SEM and roughness parameters by contact scanning instrument. The presence of Al(2)O(3) was detected by EDS and the amount calculated by digital analyses. Osteoblasts were cultured on these surfaces and it was evaluated: cell adhesion, proliferation, and viability, alkaline phosphatase activity, total protein content, and matrix mineralization formation. Physical and chemical treatments produced very different surface morphologies. Al(2)O(3) residues were detected on SB and SLA2 surfaces. Only matrix mineralization formation was affected by different surface treatments, being increased on rough surface (SLA1) and reduced on surface with high amount of Al(2)O(3) residues (SB). On the basis of these findings, it is possible to conclude that high concentration of residual Al(2)O(3) negatively interfere with the process of matrix mineralization formation in contact with Ti implant surfaces.

  2. Ventilatory Control in ALS

    PubMed Central

    Nichols, Nicole L.; Van Dyke, J.; Nashold, L.; Satriotomo, I.; Suzuki, M.; Mitchell, G.S.

    2015-01-01

    Amyotrophic lateral sclerosis (ALS) is a fatal, progressive neurodegenerative disease. ALS selectively causes degeneration in upper and lower (spinal) motor neurons, leading to muscle weakness, paralysis and death by ventilatory failure. Although ventilatory failure is generally the cause of death in ALS, little is known concerning the impact of this disorder on respiratory motor neurons, the consequences of respiratory motor neuron cell death, or the ability of the respiratory control system to “fight back” via mechanisms of compensatory respiratory plasticity. Here we review known effects of ALS on breathing, including possible effects on rhythm generation, respiratory motor neurons, and their target organs: the respiratory muscles. We consider evidence for spontaneous compensatory plasticity, preserving breathing well into disease progression despite dramatic loss of spinal respiratory motor neurons. Finally, we review current and potential therapeutic approaches directed toward preserving the capacity to breathe in ALS patients. PMID:23692930

  3. Mineral phases and metals in baghouse dust from secondary ...

    EPA Pesticide Factsheets

    Baghouse dust (BHD) is a solid waste generated by air pollution control systems during secondary aluminum processing (SAP). Management and disposal of BHD can be challenging in the U.S. and elsewhere. In this study, the mineral phases, metal content and metal leachability of 78 BHD samples collected from 13 different SAP facilities across the U.S. were investigated. The XRD semi-quantitative analysis of BHD samples suggests the presence of metallic aluminum, aluminum oxide, aluminum nitride and its oxides, spinel, elpasolite as well as diaspora. BHD also contains halite, sylvite and fluorite, which are used as fluxes in SAP activities. Total aluminum (Al) in the BHD samples averaged 18% by weight. Elevated concentrations of trace metals (>100 µgL-1 As; >1000 µgL-1 Cu, Mn, Se, Pb, Mn and Zn) were also detected in the leachate. The U.S. toxicity characteristic leaching procedure (TCLP) results showed that some samples leached above the toxicity limit for Cd, Pb and Se. Exceeding the TCLP limits in all sample is independent of facilities generating the BHD. From the metal content perspective only, it appears that BHD has a higher potential to exhibit toxicity characteristics than salt cake (the largest waste stream generated by SAP facilities). The objective of this study was to investigate BHD from SAP facilities in the U.S. by determining the mineral phases and the metal (Al, As, Ca, Cd, Cr, Cu, Fe, K, Mg, Mn, Na, Pb, Se and Zn) content of the sample

  4. Chladniite: A New Mineral Honoring the Father of Meteoritics

    NASA Astrophysics Data System (ADS)

    McCoy, T. J.; Steele, I. M.; Keil, K.; Leonard, B. F.; Endress, M.

    1993-07-01

    cell. A total of 17 lines were observed in the powder pattern. Chladniite is hexagonal, R 3(bar), a = 14.967 angstroms, c = 42.595 angstroms, beta = 120 degrees. Attempts to determine the structure of chladniite are in progress. Chladniite is named for Ernst Florens Friedrich Chladni (1756-1827), who is widely regarded as the "Father of Meteoritics." After his initial training as a lawyer, Chladni turned his attention to science, particularly problems in acoustics. He was not, however, able to obtain a permanent position and embarked upon the life of a nomad, traveling among the great cities of Europe lecturing about acoustics. During these travels, he eventually gained an interest in meteoritics. It was Chladni's pioneering book of 1794 that, for the first time, presented strong evidence for an extraterrestrial origin of meteoritic stones and irons [5]. In addition, Chladni argued that meteorites must have been the building blocks of all planets and argued that a large iron core must exist inside the Earth. During his extensive travels, Chladni also established a meteorite collection that can still be seen at Humboldt University in Berlin. It is appropriate that a mineral be named in his honor as we approach the 200th anniversary of the publication of his monumental work. References: [1] McCoy et al. (1993) Meteoritics, in press. [2] Fuchs et al. (1967) GCA, 21, 1711-1719. [3] Araki and Moore (1981) Am. Mineral., 66, 827-842. [4] Livingstone (1980) Min. Mag., 43, 833-836. [5] Chladni (1794) Riga, J. F. Hartknoch (in German); reprinted (with introduction by G. Hoppe) by Akad. Verlagsgesellschaft Geest & Portig K.-G. (1982) (in German).

  5. Mineral particles in the lungs of subjects resident in the Rome area and not occupationally exposed to mineral dust

    SciTech Connect

    Paoletti, L.; Batisti, D.; Caiazza, S.; Petrelli, M.G.; Taggi, F.; De Zorzi, L.; Dina, M.A.; Donelli, G.

    1987-10-01

    We studied the inorganic particulate contained in the lung parenchyma of 10 subjects (5 males and 5 females) residing in an urban area and not occupationally exposed to dusts. A total of 17 mineral types were identified, along with 16 metal elements in the form of oxides and sulfides. Approximately 70% of the minerals were made up of phyllosilicates, in particular clay, mica, and talc; three metal elements, Fe, Al, and Ti, accounted for more than 75% of the recovered oxide particles. The mean concentration of the observed inorganic particles was approximately 1.8 X 10(5) pp/mg dry tissue. No significant differences were observed in terms of total particulate concentration in the various areas of the lungs and between the right and left lung. Instead we observed a larger concentration of fibrous particles in the upper lobes. The analysis of the data made it possible to determine the presence of a high degree of correlation between the concentrations of silicates and the concentrations of metal oxides and sulfides, implying the existence of a ubiquitous environmental source of these mineral particles. The frequent observation of tremolite fibers is remarkable. This finding, confirmed elsewhere, indicates that the magnitude of the sources of these fibers in the environment, constituted by contaminated talc dusts, has been underestimated until today.

  6. Shock waves data for minerals

    NASA Technical Reports Server (NTRS)

    Ahrens, Thomas J.; Johnson, Mary L.

    1994-01-01

    Shock compression of the materials of planetary interiors yields data which upon comparison with density-pressure and density-sound velocity profiles constrain internal composition and temperature. Other important applications of shock wave data and related properties are found in the impact mechanics of terrestrial planets and solid satellites. Shock wave equation of state, shock-induced dynamic yielding and phase transitions, and shock temperature are discussed. In regions where a substantial phase change in the material does not occur, the relationship between the particle velocity, U(sub p), and the shock velocity, U(sub s), is given by U(sub s) = C(sub 0) + S U(sub p), where C(sub 0) is the shock velocity at infinitesimally small particle velocity, or the ambient pressure bulk sound velocity. Numerical values for the shock wave equation of state for minerals and related materials of the solar system are provided.

  7. Terminal particle from Stardust track 130: Probable Al-rich chondrule fragment from comet Wild 2

    NASA Astrophysics Data System (ADS)

    Joswiak, D. J.; Nakashima, D.; Brownlee, D. E.; Matrajt, G.; Ushikubo, T.; Kita, N. T.; Messenger, S.; Ito, M.

    2014-11-01

    A 4 × 6 μm terminal particle from Stardust track 130, named Bidi, is composed of a refractory assemblage of Fo97 olivine, Al- and Ti-bearing clinopyroxene and anorthite feldspar (An97). Mineralogically, Bidi resembles a number of components found in primitive chondritic meteorites including Al-rich chondrules, plagioclase-bearing type I ferromagnesian chondrules and amoeboid olivine aggregates (AOAs). Measured widths of augite/pigeonite lamellae in the clinopyroxene indicate fast cooling rates suggesting that Bidi is more likely to be a chondrule fragment than an AOA. Bulk element concentrations, including an Al2O3 content of 10.2 wt%, further suggests that Bidi is more akin to Al-rich rather than ferromagnesian chondrules. This is supported by high anorthite content of the plagioclase feldspar, overall bulk composition and petrogenetic analysis using a cosmochemical Al2O3-Ca2SiO4-Mg2SiO4 phase diagram. Measured minor element abundances of individual minerals in Bidi generally support an Al-rich chondrule origin but are not definitive between any of the object types. Oxygen isotope ratios obtained from olivine (+minor high-Ca pyroxene)fall between the TF and CCAM lines and overlap similar minerals from chondrules in primitive chondrites but are generally distinct from pristine AOA minerals. Oxygen isotope ratios are similar to some minerals from both Al-rich and type I ferromagnesian chondrules in unequilibrated carbonaceous, enstatite and ordinary chondrites. Although no single piece of evidence uniquely identifies Bidi as a particular object type, the preponderance of data, including mineral assemblage, bulk composition, mineral chemistry, inferred cooling rates and oxygen isotope ratios, suggest that Bidi is more closely matched to Al-rich chondrules than AOAs or plagioclase-bearing type I ferromagnesian chondrules and likely originated in a chondrule-forming region in the inner solar system.

  8. Change in mineral weathering behaviors of a bacterium Chitinophaga jiangningensis JN53 under different nutrition conditions.

    PubMed

    Cheng, Cheng; Wang, Qi; He, Linyan; Sheng, Xiafang

    2017-04-01

    Bacteria play important roles in mineral weathering and soil formation. However, little is known about the nutrition-related changes in mineral weathering potential and pattern of bacteria. In this study, mineral weathering behaviors of a novel mineral-weathering bacterium Chitinophaga jiangningensis JN53 were characterized in the presence of three contrasting biotite or potassium feldspar-added media. C. jiangningensis JN53 increased more Fe release from the minerals in the M-BHm (nutrition-poor medium) than in the SSKM (nutrition-rich medium) and BHm (nutrition-moderate medium), while C. jiangningensis JN53 released more Al from the minerals and Si from biotite in the SSKM. Similar Si release from potassium feldspar by C. jiangningensis JN53 was observed in the SSKM, BHm, and M-BHm. K releasing ability of C. jiangningensis JN53 was significantly higher in the biotite-added M-BHm. Highest and lowest growth of C. jiangningensis JN53 was observed in the SSKM and M-BHm, respectively. In the presence of the minerals, C. jiangningensis JN53 mainly produced gluconic acid in the SSKM and acetic acid in the BHm and M-BHm. C. jiangningensis JN53 also produced large amount of succinic acid in the biotite-added SSKM and oxalic acid in the potassium feldspar-added M-BHm. The results showed the growth, production of organic acids, and mineral weathering ability of C. jiangningensis JN53 in the three contrasting nutrition conditions. The results also suggested the change in the mineral weathering behaviors of C. jiangningensis JN53 under different levels of nutrition conditions.

  9. Controls on radium transport by adsorption to iron minerals

    NASA Astrophysics Data System (ADS)

    Chen, M.; Wang, T.; Kocar, B. D.

    2015-12-01

    Radium is a naturally occurring radioactive metal found in many subsurface environments. Radium isotopes are generated by uranium and thorium decay, and are particularly abundant within groundwaters where minimal porewater flux leads to accumulation. These isotopes are used as natural tracers for estimating submarine groundwater discharge (SGD) [1], allowing for large scale estimation of GW fluxes into and out of the ocean [2]. They also represent a substantial hazard in wastewater produced after hydraulic fracturing for natural gas extraction [3], resulting in a significant risk of environmental release to surface and near-surface waters, and increased cost for water treatment or disposal. Adsorption to mineral surfaces represents a dominant pathway of radium retention in subsurface environments. For SGD studies, adsorption processes impact estimates of GW fluxes, while in hydraulic fracturing, radium adsorption to aquifer solids mediates wastewater radium activities. Analysis of past sorption studies revealed large variability in partition coefficients [4], while examination of radium adsorption kinetics and surface complexation have only recently started [5]. Accordingly, we present the results of sorption and column experiments of radium with a suite of iron minerals representative of those found within deep saline and near-surface (freshwater) aquifers, and evaluate impacts of varying salinity solutions through artificial waters. Further, we explore the impacts of pyrite oxidation and ferrihydrite transformation to other iron-bearing secondary minerals on the transport and retention of radium. These results will provide critical information on the mineralogical controls on radium retention in subsurface environments, and will therefore improve predictions of radium groundwater transport in natural and contaminated systems. [1] Charette, M.A., Buesseler, K.O. & Andrews, J.E., Limnol. Oceanogr. (2001). [2] Moore, W.S., Ann. Rev. Mar. Sci. (2010). [3] Vengosh, A

  10. Was Mineral Surface Complexity and Toxicity an Impetus for Evolution of Microbial Extracellular Polymeric Substances?

    NASA Astrophysics Data System (ADS)

    Sahai, N.; Xu, J.; Zhu, C.; Campbell, J.; Hickey, W.; Zhang, N.

    2011-12-01

    Modern ecological niches are teeming with an astonishing diversity of microbial life closely associated with mineral surfaces, highlighting the remarkable success of microorganisms in conquering the challenges and capitalizing on the benefits presented by the mineral-water interface. Such community-living is enabled by an extracellular, polymeric, biofilm matrix developed at cell surfaces. Despite the energetic penalties, biofilm formation capability likely evolved on early Earth because of crucial cell survival functions, of which recognized roles include facilitating cell-attachment at mineral surfaces, intercellular signaling and lateral gene transfer, protection from dessication in tidal pools, and screening toxic UV light and toxic soluble metals. Cell-attachment to mineral surfaces was likely critical for cell survival and function, but the potential toxicity of mineral surfaces towards cells and the complexities of the mineral-water-cell interface in promoting biofilm formation, have not been fully appreciated. We examined the effects of nanoparticulate oxides (amorphous SiO2, anatase β-TiO2, and γ-Al2O3) on EPS- and biofilm-producing wild-type strains and their isogenic knock-out mutants which are defective in EPS-producing ability. In detail, we used Gram-negative wild-type Pseudomonas aeruginosa PAO1 and its EPS knock-out mutant Δ-psl, and the Gram-positive wild-type Bacillus subtilis NCIB3610 and its EPS-knock-out mutant yhxBΔ. We conducted bacterial growth experiments in the presence of each oxide in order to determine the viability of each cell type relative to oxide-free controls. The amount of EPS generated in the presence of oxides was also quantified and qualitatively analyzed by fluorescent stains. The results indicated a previously unrecognized role for microbial extracellular polymeric substances (EPS) in shielding both Gram-negative and Gram-positive cells against the toxic effects of mineral surfaces. This role is distinct from the

  11. Fluorine in the Mantle: the Role of Nominally Anhydrous Minerals

    NASA Astrophysics Data System (ADS)

    Mosenfelder, J. L.; Rossman, G. R.

    2012-12-01

    indicated by experimental studies [3,4,7], which consistently find mineral-melt partition coefficients following the order cpx>opx>gt>ol. 3) Contrary to the study of Beyer et al. [3] but in accord with the results of Dalou et al. [4], we find no overall correlation between Al and F in pyroxenes. 4) Results so far suggest that H and F co-substitute in garnets, but are decoupled in other NAMs. Beyer et al. [3] have suggested that the F budget of the mantle can be entirely accommodated by F incorporation in NAMs, and our results are in accord with their calculations. We speculate that F within mantle NAMs may exert an important influence on melting, but probably has much less of an effect compared to hydrogen - or even no effect at all - on other processes or properties such as deformation, chemical diffusion, viscosity, and electrical conductivity. [1] Smith et al. (1981), Lithos, 14, 133-147. [2] Hervig and Bell (2005), Fall AGU 2005 abstract [3] Beyer et al. (2012), EPSL, 337-338, 1-9 [4] Dalou et al. (2012), CMP [5] Bell and Rossman , 1992, Science, 255, 1391-1397 [6] Mosenfelder et al. (2011), 96, 1725-1741. [7] Hauri et al. (2006), EPSL, 248, 715-734.

  12. Minerals Yearbook, 1988. The mineral industries of the Arabian Peninsula and Persian Gulf countries. International review

    SciTech Connect

    Michalski, B.; Antonides, L.E.; Morgan, G.A.

    1988-01-01

    The document contains commodity reviews (metals, mineral fuels, industrial minerals where applicable) for the following countries: Bahrain, Iran, Iraq, Kuwait, Oman, Qatar, Saudi Arabia, United Arab Emirates, People's Democratic Republic of Yeman, and Yeman Arab Republic.

  13. Diamond and Unusual Minerals Discovered from the Chromitite in Polar Ural: A First Report

    NASA Astrophysics Data System (ADS)

    Yang, J.; Bai, W.; Fang, Q.; Meng, F.; Chen, S.; Zhang, Z.

    2007-12-01

    Ultrahigh pressure (UHP) minerals, such as diamond, coesite, and pseudomorphs of octahedral olivine, and as well as about 80 other mineral species have been recovered from podiform chromitites of the Luobusa ophiolite, southern Tibet, and a new mineral, Luobusaite (Fe0.82Si2), has been approved recently by CNMMN. The UHP minerals from Luobusa are controversial because they have not found in situ and because ophiolites are currently believed to form at shallow levels above oceanic spreading centers. More detailed study and experimental work are needed to understand the origin and significance of these unusual minerals and investigations of other ophiolites are needed to determine if such minerals occur elsewhere. For this purpose, we collected about 1500 kg of chromitite from two orebodies in an ultramafic body in the Polar Urals. Thus far, more than 60 different mineral species have been separated from these ores. The most exciting discovery is the common occurrence of diamond, a typical UHP mineral in the Luobusa chromitites. Diamonds from Ural chromitite are clear, colorless, well-developed crystals with octahedral morphology, generally 0.2-0.3 mm in size. Attached with the diamonds and perhaps also occurring as inclusions within them are many minerals as chromite, MnNiCrFe alloy, native Si and Ta, corundum, zircon, feldspar, garnet, moissanite, confirming their natural origin and suggesting a long residence time in the mantle. Other mineral group include: (1) native elements: Cr, W, Ni, Co, Si, Al and Ta; (2) carbides: SiC and WC; (3) alloys: Cr-Fe, Si-Al-Fe, Ni-Cu, Ag-Au, Ag-Sn, Fe-Si, Fe-P, and Ag-Zn-Sn; (4) oxides: NiCrFe, PbSn, REE, rutile and Si- bearing rutile, ilmenite, corundum, chromite, MgO, and SnO2; (5) silicates: kyanite, pseudomorphs of octahedral olivine, zircon, garnet, feldspar, and quartz,; (6) sulfides of Fe, Ni, Cu, Mo, Pb, Ab, AsFe, FeNi, CuZn, and CoFeNi; and (7) iron groups: native Fe, FeO, and Fe2O3. These minerals are very similar in

  14. Cancrinite-group minerals behavior at non-ambient conditions

    NASA Astrophysics Data System (ADS)

    Lotti, Paolo; Gatta, G. Diego; Kahlenberg, Volker; Merlini, Marco; Alvaro, Matteo; Cámara, Fernando

    2014-05-01

    Cancrinite-group minerals occur in the late stages of alkaline (SiO2)-undersaturated magmatism and in related effusive or contact rocks. So far only few studies have been devoted to the description of the thermo-elastic behavior, phase-stability and P /T -structure evolution (at the atomic scale) of this mineral group. Cancrinite-group minerals have an open-framework structure characterized by the [CAN]-topology. The [CAN]-framework shows large 12-ring channels, parallel to the c crystallographic axis, bound by columns of cages, the so-called can units. While very limited chemical variation is observed in the framework composition (the composition is almost always [Si6Al6O24]) a remarkable chemical variability is reported for the extraframework components in the cancrinite-group minerals. Two subgroups can be identified according to the extraframework content of the can units: the cancrinite- and the davyne-subgroups, showing Na-H2O and Ca-Cl chains, respectively. The channels are stuffed by cations, anions and molecules. We aimed to model the thermo-elastic behavior and the mechanisms of the (P ,T)-induced structure evolution of cancrinite-group minerals, with special interest on the role played by the extraframework population. The study was restricted to the following (CO3)-rich and (SO4)-rich end-members: cancrinite sensu stricto {[(Na,Ca)6(CO3)1.2-1.7][Na2(H2O)2][Al6Si6O24]}, vishnevite {[(Na,Ca,K)6(SO4)][Na2(H2O)2][Al6Si6O24]}, balliranoite {[(Na,Ca)6(CO3)1.2-1.7][Ca2Cl2][Al6Si6O24]} and davyne {[(Na,Ca,K)6((SO4),Cl)][Ca2Cl2][Al6Si6O24]}. Their high-P and low-T (T < 293 K) behavior was investigated by means of in-situ single-crystal X-ray diffraction, using diamond-anvil cells and (N2)-cryosystems, respectively. The high-T behavior of cancrinite has also been studied by means of in-situ single-crystal X-ray diffraction with a resistive heater. Cancrinite minerals share a similar volume compressibility and thermal expansivity at ambient conditions (cancrinite

  15. The nanophase iron mineral(s) in Mars soil

    NASA Technical Reports Server (NTRS)

    Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Mancinelli, R. L.; Gehring, A. U.

    1993-01-01

    A series of surface-modified clays containing nanophase (np) iron oxide/oxyhydroxides of extremely small particle sizes, with total iron contents as high as found in Mars soil, were prepared by iron deposition on the clay surface from ferrous chloride solution. Comprehensive studies of the iron mineralogy in these "Mars-soil analogs" were conducted using chemical extractions, solubility analyses, pH and redox, x ray and electron diffractometry, electron microscopic imaging, specific surface area and particle size determinations, differential thermal analyses, magnetic properties characterization, spectral reflectance, and Viking biology simulation experiments. The clay matrix and the procedure used for synthesis produced nanophase iron oxides containing a certain proportion of divalent iron, which slowly converts to more stable, fully oxidized iron minerals. The clay acted as an effective matrix, both chemically and sterically, preventing the major part of the synthesized iron oxides from ripening, i.e., growing and developing larger crystals. The precipitated iron oxides appear as isodiametric or slightly elongated particles in the size range 1-10 nm, having large specific surface area. The noncrystalline nature of the iron compounds precipitated on the surface of the clay was verified by their complete extractability in oxalate. Lepidocrocite (gamma-FeOOH) was detected by selected area electron diffraction. It is formed from a double iron Fe(II)/Fe(III) hydroxy mineral such as "green rust," or ferrosic hydroxide. Magnetic measurements suggested that lepidocrocite converted to the more stable maghemite (gamma-Fe2O3) by mild heat treatment and then to nanophase hematite (alpha-Fe2O3) by extensive heat treatment. After mild heating, the iron-enriched clay became slightly magnetic, to the extent that it adheres to a hand-held magnet, as was observed with Mars soil. The chemical reactivity of the iron-enriched clays strongly resembles, and offers a plausible mechanism

  16. The Moon: Determining Minerals and their Abundances with Mid-IR Spectral Deconvolution II

    NASA Astrophysics Data System (ADS)

    Kozlowski, Richard W.; Donaldson Hanna, K.; Sprague, A. L.; Grosse, F. A.; Boop, T. S.; Warell, J.; Boccafola, K.

    2007-10-01

    We determine the mineral compositions and abundances at three locations on the lunar surface using an established spectral deconvolution algorithm (Ramsey 1996, Ph.D. Dissertation, ASU; Ramsey and Christiansen 1998, JGR 103, 577-596) for mid-infrared spectral libraries of mineral separates of varying grain sizes. Spectral measurements of the lunar surface were obtained at the Infrared Telescope Facility (IRTF) on Mauna Kea, HI with Boston University's Mid-Infrared Spectrometer and Imager (MIRSI). Our chosen locations, Aristarchus, Grimaldi and Mersenius C, have been previously observed in the VIS near-IR from ground-based telescopes and spacecraft (Zisk et al. 1977, The Moon 17, 59-99; Hawke et al. 1993, GRL 20, 419-422; McEwen et al. 1994, Science 266, 1858-1862; Peterson et al. 1995, 22, 3055-3058; Warell et al. 2006, Icarus 180, 281-291), however there are no sample returns for analysis. Surface mineral deconvolutions of the Grimaldi Basin infill are suggestive of anorthosite, labradorite, orthopyroxene, olivine, garnet and phosphate. Peterson et al. (1995) indicated the infill of Grimaldi Basin has a noritic anorthosite or anorthositic norite composition. Our spectral deconvolution supports these results. Modeling of other lunar locations is underway. We have also successfully modeled laboratory spectra of HED meteorites, Vesta, and Mercury (see meteorites and mercurian abstracts this meeting). These results demonstrate the spectral deconvolution method to be robust for making mineral identifications on remotely observed objects, in particular main-belt asteroids, the Moon, and Mercury. This work was funded by NSF AST406796.

  17. U.S. Geological Survey Minerals Yearbook—Metals and Minerals

    USGS Publications Warehouse

    ,

    2016-01-01

    This edition of the U.S. Geological Survey (USGS) Minerals Yearbook discusses the performance of the worldwide minerals and materials industries during 2012 and provides background information to assist in interpreting that performance. Content of the individual Minerals Yearbook volumes follows:• Volume I, Metals and Minerals, contains chapters about virtually all metallic and industrial mineral commodities important to the U.S. economy. Chapters on survey methods, summary statistics for domestic nonfuel minerals, and trends in mining and quarrying in the metals and industrial mineral industries in the United States are also included.• Volume II, Area Reports: Domestic, contains a chapter on the mineral industry of each of the 50 States and Puerto Rico and the Administered Islands. This volume also has chapters on survey methods and summary statistics of domestic nonfuel minerals.• Volume III, Area Reports: International, is published as four separate reports. These regional reports contain the latest available minerals data on more than 180 foreign countries and discuss the importance of minerals to the economies of these nations and the United States. Each report begins with an overview of the region’s mineral industries during the year. It continues with individual country chapters that examine the mining, refining, processing, and use of minerals in each country of the region and how each country’s mineral industry relates to U.S. industry. Most chapters include production tables and industry structure tables, information about Government policies and programs that affect the country’s mineral industry, and an outlook section.The USGS continually strives to improve the value of its publications to users. Constructive comments and suggestions by readers of the Minerals Yearbook are welcomed.

  18. Minerals yearbook: Mineral industries of Africa. Volume 3. 1992 international review

    SciTech Connect

    Not Available

    1992-01-01

    The 53 countries that constituted Africa in 1992 accounted for a significant portion of total world output of a number of mineral commodities. Among the most significant mineral commodities produced in Africa were andalusite, antimony, asbestos, bauxite, chromite, coal, cobalt, copper, diamond, fluorspar, gold, lithium minerals, manganese, phosphate, platinum-group metals, the titanium minerals-ilmenite and rutile, vanadium, vermiculite, uranium, and zircon. Chromite, cobalt, and manganese, were not mined in the Untied States.

  19. Weathering of Fe-bearing minerals under Martian conditions, investigated by Mössbauer spectroscopy

    NASA Astrophysics Data System (ADS)

    Schröder, C.; Klingelhöfer, G.; Tremel, W.

    2004-09-01

    The surface of Mars is covered by weathered material. Mars' rusty red colour in particular is commonly ascribed to ferric iron-bearing minerals. The planet's surface is generally iron rich. Mössbauer spectroscopy is a powerful tool for quantitative mineralogical analysis of Fe-bearing minerals. Consequently, the miniaturized Mössbauer spectrometer MIMOS II is part of the payload of NASA's twin Mars Exploration Rovers "Spirit" and "Opportunity", and ESA's ill-fated Mars Express lander "Beagle 2". Both Mars Exploration Rovers are currently conducting successful surface operations on Mars. In this paper, we give a brief insight into mission operations with respect to the reconstruction of local weathering scenarios at the landing sites, which in turn will help to illuminate the climatic history of the planet. Mössbauer spectra obtained in preparation of the mission from the SNC meteorites Nakhla, Dar al Gani 476, and Sayh al Uhaymir, show weathering and other alteration features. Preliminary results of laboratory weathering experiments on Fe-bearing minerals (olivine and pyroxene) show the importance of analysing individual minerals to understand weathering of more complex mineral assemblages like, e.g., basalt.

  20. Double layer hydroxide minerals as host structures for bioorganic molecules. [Abstract only

    NASA Technical Reports Server (NTRS)

    Lee, Ton; Arrhenius, Meichia L.; Hui, Stella S.-Y.; Ring, Ken M.; Gedulin, Benjamin I.; Orgel, Leslie E.; Arrhenius, Gustaf

    1994-01-01

    A central problem in molecular evolution concerns the selective concentration from dilute, multicomponent solution of source molecules into a reactive environment, where formation of larger molecular assemblages can take place. Minerals consisting of positively charged, separable metal hydroxide sheets have proven capable of these functions. This common structural type is represented by minerals such as pyroaurite (Mg-Fe(3+) hydroxide), hydrotalcite (Mg-Al), green rust Fe(2+)-Fe(3+) and others. Effective interlayer sorption is demonstrated for orthophosphate and condensed phosphates, anionic alkyl compounds, polypeptides, nucleic acids, cyanide complexes and glycolaldehyde phosphate, the latter shown to readily oligomerize to form and selectively retain racemic hexose -2, 4, 6-phosphates, preferentially of altrose (Pitsch, et al, 1993). The selective aldomerization and retention effects correlate with the charge distribution in the host mineral structure and the stereochemistry of the substrate molecules. Interaction between nucleic acid bases, and between the cyanide groups of glycolaldehyde phosphate nitrile at the low water activity in the mineral interlayer is indicated by doubling of the monomeric separation of the hydroxide mineral sheets.

  1. 43 CFR 3594.5 - Minerals soluble in water; brines; minerals taken in solution.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... water; brines; minerals taken in solution. (a) In mining or prospecting deposits of sodium, potassium or other minerals soluble in water, all wells, shafts, prospecting holes and other openings shall be... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false Minerals soluble in water;...

  2. 43 CFR 3594.5 - Minerals soluble in water; brines; minerals taken in solution.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... water; brines; minerals taken in solution. (a) In mining or prospecting deposits of sodium, potassium or other minerals soluble in water, all wells, shafts, prospecting holes and other openings shall be... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false Minerals soluble in water;...

  3. 43 CFR 3594.5 - Minerals soluble in water; brines; minerals taken in solution.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... water; brines; minerals taken in solution. (a) In mining or prospecting deposits of sodium, potassium or other minerals soluble in water, all wells, shafts, prospecting holes and other openings shall be... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false Minerals soluble in water;...

  4. 43 CFR 3000.8 - Management of Federal minerals from reserved mineral estates.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false Management of Federal minerals from reserved mineral estates. 3000.8 Section 3000.8 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000)...

  5. 43 CFR 3000.8 - Management of Federal minerals from reserved mineral estates.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false Management of Federal minerals from reserved mineral estates. 3000.8 Section 3000.8 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000)...

  6. 43 CFR 3594.5 - Minerals soluble in water; brines; minerals taken in solution.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false Minerals soluble in water; brines; minerals taken in solution. 3594.5 Section 3594.5 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000)...

  7. 43 CFR 3000.8 - Management of Federal minerals from reserved mineral estates.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false Management of Federal minerals from reserved mineral estates. 3000.8 Section 3000.8 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000)...

  8. 43 CFR 3000.8 - Management of Federal minerals from reserved mineral estates.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false Management of Federal minerals from reserved mineral estates. 3000.8 Section 3000.8 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR MINERALS MANAGEMENT (3000)...

  9. Bone mineral measurement from Apollo experiment M-078. [derangement of bone mineral metabolism in spacecrews

    NASA Technical Reports Server (NTRS)

    Vogel, J. M.; Rambaut, P. C.; Smith, M. C., Jr.

    1974-01-01

    Loss of mineral from bone during periods of immobilization, recumbency, or weightlessness is examined. This report describes the instrumentation, technique, and bone mineral changes observed preflight and postflight for the Apollo 14, 15, and 16 missions. The bone mineral changes documented during the Apollo Program are reviewed, and their relevance to future missions is discussed.

  10. ALS2 mutations

    PubMed Central

    Schneider, Susanne A.; Carr, Lucinda; Deuschl, Guenther; Hopfner, Franziska; Stamelou, Maria; Wood, Nicholas W.; Bhatia, Kailash P.

    2014-01-01

    Objective: To determine the genetic etiology in 2 consanguineous families who presented a novel phenotype of autosomal recessive juvenile amyotrophic lateral sclerosis associated with generalized dystonia. Methods: A combination of homozygosity mapping and whole-exome sequencing in the first family and Sanger sequencing of candidate genes in the second family were used. Results: Both families were found to have homozygous loss-of-function mutations in the amyotrophic lateral sclerosis 2 (juvenile) (ALS2) gene. Conclusions: We report generalized dystonia and cerebellar signs in association with ALS2-related disease. We suggest that the ALS2 gene should be screened for mutations in patients who present with a similar phenotype. PMID:24562058

  11. Mineral losses during extreme environmental conditions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Minerals are nutrients that are conserved by the body. During exposure to environmental stimuli, such as heat and/or exercise, the excretion of minerals, macro (Na, K, Ca, Mg) and micro (Cu, Fe, Zn), occurs through the body surface in the form of cellular desquamation and sweat, as well as in the u...

  12. Earth mineral resource of the month: asbestos

    USGS Publications Warehouse

    Virta, Robert L.

    2010-01-01

    The article discusses the characteristics and feature of asbestos. According to the author, asbestos is a generic name for six needle-shaped minerals that possess high tensile strengths, flexibility, and resistance to chemical and thermal degradation. These minerals are actinolite, amosite, anthophyllite, chrysolite, crocilodite and tremolite. Asbestos is used for strengthening concrete pipe, plastic components, and gypsum plasters.

  13. Mineral resource of the month: tantalum

    USGS Publications Warehouse

    ,

    2011-01-01

    The article offers information on a rare transition metal called tantalum. It says that the blue-gray mineral resource was discovered in 1801 or 1802 and was used for capacitors in 1940. It adds that the tantalite ore and other minerals in the ore should be separated in order to generate concentrates of tantalum. The use of tantalum are also cited.

  14. ASEAN Mineral Database and Information System (AMDIS)

    NASA Astrophysics Data System (ADS)

    Okubo, Y.; Ohno, T.; Bandibas, J. C.; Wakita, K.; Oki, Y.; Takahashi, Y.

    2014-12-01

    AMDIS has lunched officially since the Fourth ASEAN Ministerial Meeting on Minerals on 28 November 2013. In cooperation with Geological Survey of Japan, the web-based GIS was developed using Free and Open Source Software (FOSS) and the Open Geospatial Consortium (OGC) standards. The system is composed of the local databases and the centralized GIS. The local databases created and updated using the centralized GIS are accessible from the portal site. The system introduces distinct advantages over traditional GIS. Those are a global reach, a large number of users, better cross-platform capability, charge free for users, charge free for provider, easy to use, and unified updates. Raising transparency of mineral information to mining companies and to the public, AMDIS shows that mineral resources are abundant throughout the ASEAN region; however, there are many datum vacancies. We understand that such problems occur because of insufficient governance of mineral resources. Mineral governance we refer to is a concept that enforces and maximizes the capacity and systems of government institutions that manages minerals sector. The elements of mineral governance include a) strengthening of information infrastructure facility, b) technological and legal capacities of state-owned mining companies to fully-engage with mining sponsors, c) government-led management of mining projects by supporting the project implementation units, d) government capacity in mineral management such as the control and monitoring of mining operations, and e) facilitation of regional and local development plans and its implementation with the private sector.

  15. Minerals yearbook, 1990: Idaho. Annual report

    SciTech Connect

    Minarik, R.J.; Gillerman, V.S.

    1992-09-01

    The 1990 Annual Report is on the Mineral Industry of Idaho. Idaho ranked 26th nationally for total mineral production value compared with 28th in 1989. The State was first in the Nation in antimony and garnet production; second in silver and vandaium production; and third in output of lead, molybdenum, and marketable phosphate rock.

  16. Killer clays! Natural antibacterial clay minerals

    USGS Publications Warehouse

    Williams, L.B.; Holland, M.; Eberl, D.D.; Brunet, T.; De Courrsou, L. B.

    2004-01-01

    The clay chemical properties that may be important in medicine were investigated. It was found that natural clay minerals can have striking and very specific effects on microbial populations. The effects can range from potentially enhanced microbial growth to complete sterilization. This paper presents evidence that natural clay minerals can be effective antimicrobial agents.

  17. 36 CFR 292.18 - Mineral resources.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 36 Parks, Forests, and Public Property 2 2011-07-01 2011-07-01 false Mineral resources. 292.18 Section 292.18 Parks, Forests, and Public Property FOREST SERVICE, DEPARTMENT OF AGRICULTURE NATIONAL RECREATION AREAS Sawtooth National Recreation Area-Federal Lands § 292.18 Mineral resources. (a)...

  18. 43 CFR 9239.5 - Minerals.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 43 Public Lands: Interior 2 2012-10-01 2012-10-01 false Minerals. 9239.5 Section 9239.5 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR TECHNICAL SERVICES (9000) TRESPASS Kinds of Trespass § 9239.5 Minerals....

  19. 43 CFR 9239.5 - Minerals.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 43 Public Lands: Interior 2 2014-10-01 2014-10-01 false Minerals. 9239.5 Section 9239.5 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR TECHNICAL SERVICES (9000) TRESPASS Kinds of Trespass § 9239.5 Minerals....

  20. Mineral composition of serial slaughter Holstesin carcasses

    Technology Transfer Automated Retrieval System (TEKTRAN)

    In order to determine the mineral requirements of cattle it is necessary to understand the quantity of minerals that are retained in the tissues of the animal as it grows. However, the data currently used to estimate these values by the National Research Council is over 60 years old and probably doe...

  1. 36 CFR 292.18 - Mineral resources.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 36 Parks, Forests, and Public Property 2 2014-07-01 2014-07-01 false Mineral resources. 292.18 Section 292.18 Parks, Forests, and Public Property FOREST SERVICE, DEPARTMENT OF AGRICULTURE NATIONAL RECREATION AREAS Sawtooth National Recreation Area-Federal Lands § 292.18 Mineral resources. (a)...

  2. 43 CFR 9239.5 - Minerals.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 2 2011-10-01 2011-10-01 false Minerals. 9239.5 Section 9239.5 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR TECHNICAL SERVICES (9000) TRESPASS Kinds of Trespass § 9239.5 Minerals....

  3. 43 CFR 9239.5 - Minerals.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 43 Public Lands: Interior 2 2013-10-01 2013-10-01 false Minerals. 9239.5 Section 9239.5 Public Lands: Interior Regulations Relating to Public Lands (Continued) BUREAU OF LAND MANAGEMENT, DEPARTMENT OF THE INTERIOR TECHNICAL SERVICES (9000) TRESPASS Kinds of Trespass § 9239.5 Minerals....

  4. 76 FR 44892 - Information Collection; Locatable Minerals

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-27

    ... Geology Management Staff, Mail Stop 1126, 1601 N. Kent Street, 5th Floor, Arlington, VA 22209. Comments... may inspect comments received at USDA Forest Service, Minerals and Geology Management Staff, 1601 N...: Tony Ferguson, Director, Minerals and Geology Management, at 703-605-4785. Individuals who...

  5. Mineral Resource of the Month: Graphite

    USGS Publications Warehouse

    Olson, Donald W.

    2008-01-01

    Graphite, a grayish black opaque mineral with a metallic luster, is one of four forms of pure crystalline carbon (the others are carbon nanotubes, diamonds and fullerenes). It is one of the softest minerals and it exhibits perfect basal (one-plane) cleavage. Graphite is the most electrically and thermally conductive of the nonmetals, and it is chemically inert.

  6. Mineral resource of the month: potash

    USGS Publications Warehouse

    Jasinski, Stephen M.

    2011-01-01

    The article offers basic information about the mineral resource potash. According to the author, potash is the generic term for a variety of mined and manufactured salts that contain the mineral potassium in a water-soluble form. The author adds that potash is used in fertilizers, soaps and detergents, glass and ceramics, and alkaline batteries.

  7. A Cooperative Approach To Teaching Mineral Identification.

    ERIC Educational Resources Information Center

    Constantopoulos, Terri Lynn

    1994-01-01

    Describes Jigsaw Teaching, a cooperative learning approach, in relation to mineral identification. This technique may also be applied to rock identification. Students work in groups of four and learn to identify 20 minerals, becoming an "expert" on five of them. Helping to teach other students reinforces what each student has learned.…

  8. Mineral resource of the month: Strontium

    USGS Publications Warehouse

    Ober, Joyce A.

    2014-01-01

    Strontium occurs commonly in nature, ranking as the 15th most abundant chemical element on Earth. Only two minerals contain sufficient strontium, however, to be used commercially to produce strontium compounds: Strontianite (strontium carbonate) has a higher strontium content, but celestite (strontium sulfate) is by far the most abundant strontium mineral.

  9. ELECTROCHEMICAL PROPERTIES OF ROCKS AND MINERALS.

    USGS Publications Warehouse

    Olhoeft, Gary R.

    1985-01-01

    Many phenomena and processes in the earth sciences are a result of the electrochemical properties of rocks and minerals. Examples include formation of mineral deposits and petroleum reservoirs control of drilling muds, and success or failure of toxic waste isolation barriers. Such phenomena can be observed at a distance using geophysical techniques to measure various electrical properties of the earth.

  10. Mineral resource of the month: Phosphate rock

    USGS Publications Warehouse

    Jasinski, Stephen M.

    2013-01-01

    As a mineral resource, “phosphate rock” is defined as unprocessed ore and processed concentrates that contain some form of apatite, a group of calcium phosphate minerals that is the primary source for phosphorus in phosphate fertilizers, which are vital to agriculture.

  11. Monitoring genotoxic exposure in uranium miners

    SciTech Connect

    Sram, R.J.; Binkova, B.; Dobias, L.; Roessner, P.T.; Topinka, J.; Vesela, D.; Vesely, D.; Stejskalova, J.; Bavorova, H.; Rericha, V. )

    1993-03-01

    Recent data from deep uranium mines in Czechoslovakia indicated that in addition to radon daughter products, miners are also exposed to chemical mutagens. Mycotoxins were identified as a possible source of mutagenicity present in the mines. Various methods of biomonitoring were used to examine three groups of miners from different uranium mines. Cytogenetic analysis of peripheral lymphocytes, unscheduled DNA synthesis (UDS) in lymphocytes, and lipid peroxidation (LPO) in both plasma and lymphocytes were studied on 66 exposed miners and 56 controls. Throat swabs were taken from 116 miners and 78 controls. Significantly increased numbers of aberrant cells were found in all groups of miners, as well as decreased UDS values in lymphocytes and increased LPO plasma levels in comparison to controls. Molds were detected in throat swabs from 27% of miners, and 58% of these molds were embryotoxic. Only 5% of the control samples contained molds and none of them was embryotoxic. The following mycotoxins were isolated from miners' throat swab samples: rugulosin, sterigmatocystin, mycophenolic acid, brevianamid A, citreoviridin, citrinin, penicilic acid, and secalonic acid. These data suggest that mycotoxins are a genotoxic factor affecting uranium miners.

  12. Dehydration-induced luminescence in clay minerals

    NASA Technical Reports Server (NTRS)

    Coyne, L. M.; Lahav, N.; Lawless, J. G.

    1981-01-01

    Reports of triboluminescent phenomena in organic crystalline materials prompted a search for related processes in clay minerals. The reported extensive mechanical distortion produced on freezing and drying of montmorillonite was particularly interesting because of studies of condensation reactions in a wet/dry cycled reaction sequence. The discovery of an unusual luminescent process in several clay minerals is reported and its characteristics are described.

  13. The Interfacial Behavior between Biochar and Soil Minerals and Its Effect on Biochar Stability.

    PubMed

    Yang, Fan; Zhao, Ling; Gao, Bin; Xu, Xiaoyun; Cao, Xinde

    2016-03-01

    In this study, FeCl3, AlCl3, CaCl2, and kaolinite were selected as model soil minerals and incubated with walnut shell derived biochar for 3 months and the incubated biochar was then separated for the investigation of biochar-mineral interfacial behavior using XRD and SEM-EDS. The XPS, TGA, and H2O2 oxidation were applied to evaluate effects of the interaction on the stability of biochar. Fe8O8(OH)8Cl1.35 and AlCl3·6H2O were newly formed on the biochar surface or inside of the biochar pores. At the biochar-mineral interface, organometallic complexes such as Fe-O-C were generated. All the 4 minerals enhanced the oxidation resistance of biochar surface by decreasing the relative contents of C-O, C═O, and COOH from 36.3% to 16.6-26.5%. Oxidation resistance of entire biochar particles was greatly increased with C losses in H2O2 oxidation decreasing by 13.4-79.6%, and the C recalcitrance index (R50,bicohar) in TGA analysis increasing from 44.6% to 45.9-49.6%. Enhanced oxidation resistance of biochar surface was likely due to the physical isolation from newly formed minerals, while organometallic complex formation was probably responsible for the increase in oxidation resistance of entire biochar particles. Results indicated that mineral-rich soils seemed to be a beneficial environment for biochar since soil minerals could increase biochar stability, which displays an important environmental significance of biochar for long-term carbon sequestration.

  14. Control of Vertebrate Skeletal Mineralization by Polyphosphates

    PubMed Central

    Omelon, Sidney; Georgiou, John; Henneman, Zachary J.; Wise, Lisa M.; Sukhu, Balram; Hunt, Tanya; Wynnyckyj, Chrystia; Holmyard, Douglas; Bielecki, Ryszard; Grynpas, Marc D.

    2009-01-01

    Background Skeletons are formed in a wide variety of shapes, sizes, and compositions of organic and mineral components. Many invertebrate skeletons are constructed from carbonate or silicate minerals, whereas vertebrate skeletons are instead composed of a calcium phosphate mineral known as apatite. No one yet knows why the dynamic vertebrate skeleton, which is continually rebuilt, repaired, and resorbed during growth and normal remodeling, is composed of apatite. Nor is the control of bone and calcifying cartilage mineralization well understood, though it is thought to be associated with phosphate-cleaving proteins. Researchers have assumed that skeletal mineralization is also associated with non-crystalline, calcium- and phosphate-containing electron-dense granules that have been detected in vertebrate skeletal tissue prepared under non-aqueous conditions. Again, however, the role of these granules remains poorly understood. Here, we review bone and growth plate mineralization before showing that polymers of phosphate ions (polyphosphates: (PO3−)n) are co-located with mineralizing cartilage and resorbing bone. We propose that the electron-dense granules contain polyphosphates, and explain how these polyphosphates may play an important role in apatite biomineralization. Principal Findings/Methodology The enzymatic formation (condensation) and destruction (hydrolytic degradation) of polyphosphates offers a simple mechanism for enzymatic control of phosphate accumulation and the relative saturation of apatite. Under circumstances in which apatite mineral formation is undesirable, such as within cartilage tissue or during bone resorption, the production of polyphosphates reduces the free orthophosphate (PO43−) concentration while permitting the accumulation of a high total PO43− concentration. Sequestering calcium into amorphous calcium polyphosphate complexes can reduce the concentration of free calcium. The resulting reduction of both free PO43− and free

  15. High spectral resolution reflectance spectroscopy of minerals

    NASA Technical Reports Server (NTRS)

    Clark, Roger N.; King, Trude V. V.; Klejwa, Matthew; Swayze, Gregg A.; Vergo, Norma

    1990-01-01

    The reflectance spectra of minerals are studied as a function of spectral resolution in the range from 0.2 to 3.0 microns. Selected absorption bands were studied at resolving powers as high as 2240. At resolving powers of approximately 1000, many OH-bearing minerals show diagnostic sharp absorptions at the resolution limit. At low resolution, some minerals may not be distinguishable, but as the resolution is increased, most can be easily identified. As the resolution is increased, many minerals show fine structure, particularly in the OH-stretching overtone region near 1.4 micron. The fine structure can enhance the ability to discriminate between minerals, and in some cases the fine structure can be used to determine elemental composition.

  16. Two centuries of mineral policy in Wisconsin

    SciTech Connect

    Ostrom, M.E.

    1983-01-01

    Wisconsin has experienced several major shifts in mineral policy which reflect changing public attitudes about resources. Early law either encouraged mineral development or was mute during the territory and early statehood period because the prevalent attitude was for rapid development to generate capital which would foster economic growth and development. The development push of the 19th century was followed by a slow shift to environmental and social consciousness. This shift subverted Wisconsin's relationship to and dependence on outside sources of mineals and its posture with regard to mineral developent. Development is now strongly controlled by laws, land access, and social responsibility. Increased mineral dependence and high consumer prices are the price which society pays for such policies, and the author suggests the need for a national minerals policy to serve as a model for the states. 3 references.

  17. Destabilization of emulsions by natural minerals.

    PubMed

    Yuan, Songhu; Tong, Man; Wu, Gaoming

    2011-09-15

    This study developed a novel method to destabilize emulsions and recycle oils, particularly for emulsified wastewater treatment. Natural minerals were used as demulsifying agents, two kinds of emulsions collected from medical and steel industry were treated. The addition of natural minerals, including artificial zeolite, natural zeolite, diatomite, bentonite and natural soil, could effectively destabilize both emulsions at pH 1 and 60 °C. Over 90% of chemical oxygen demand (COD) can be removed after treatment. Medical emulsion can be even destabilized by artificial zeolite at ambient temperature. The mechanism for emulsion destabilization by minerals was suggested as the decreased electrostatic repulsion at low pH, the enhanced gathering of oil microdroplets at elevated temperature, and the further decreased surface potential by the addition of minerals. Both flocculation and coalescence were enhanced by the addition of minerals at low pH and elevated temperature.

  18. [Research progress of traditional mineral Chinese medicine].

    PubMed

    Chen, Bing-Chun; Zheng, Li-Li; Wang, Hai-Yan; Dong, Wei; Fu, Xian-Jun; Wang, Yu

    2014-01-01

    Traditional mineral Chinese medicine is a characteristic part of Chinese medicine, in the development of traditional Chinese medicine has its unique role. With the development of science and technology and the increase of the medical level, traditional mineral medicine research is gradually thorough and wide-ranging. In recent years, traditional mineral Chinese medicine research mainly includes the physical properties of mineral medicine, structure, chemical composition, pharmacology and treatment mechanism research. The above several aspects of research in the mineral medicine has important practical and theoretical significance. The above several aspects of research status and the problems existing in the research were briefly summarized and reviewed in this paper, and its development were discussed, to provide reference for further studies in the future.

  19. Mineral exploration with ERTS imagery. [Colorado

    NASA Technical Reports Server (NTRS)

    Nicolais, S. M.

    1974-01-01

    Ten potential target areas for metallic mineral exploration were selected on the basis of a photo-lineament interpretation of the ERTS image 1172-17141 in central Colorado. An evaluation of bias indicated that prior geologic knowledge of the region had little, if any, effect on target selection. In addition, a contoured plot of the frequency of photo-lineament intersections was made to determine what relationships exist between the photo-lineaments and mineral districts. Comparison of this plot with a plot of the mineral districts indicates that areas with a high frequency of intersections commonly coincide with known mineral districts. The results of this experiment suggest that photo-lineaments are fractures or fracture-controlled features, and their distribution may be a guide to metallic mineral deposits in Colorado, and probably other areas as well.

  20. Underground coal miners' foot and boot problems.

    PubMed

    Wood, G; Marr, S; Berry, G; Nubé, V; Cole, J

    1999-11-01

    The New South Wales (NSW) Joint Coal Board Health and Safety Trust funded an investigation into foot problems reported by 400 randomly selected underground coal miners from 15 mines in NSW. Miners were interviewed and their responses were entered directly into laptop computers. Digital cameras were also used to take pictures of skin conditions and miners' posture. Observations of the skin results indicate that miners find gumboots to be hot, sweaty and uncomfortable. Skin breakdown and tinea, is frequent and disabling and responsible for absences from the workforce that are costly for both miner and employer. A more comfortable and better designed boot is needed, fabricated in waterproof leather together with socks that 'wick' the moisture away from the foot. Socks worn were of varying components and washed at irregular intervals, indicating a need for regular changes of socks and improved hygiene.