Sample records for kakul phosphorite deposits

  1. Geochemistry and depositional environments of Paleocene-Eocene phosphorites: Metlaoui Group, Tunisia

    NASA Astrophysics Data System (ADS)

    Garnit, Hechmi; Bouhlel, Salah; Jarvis, Ian

    2017-10-01

    The Late Paleocene-Early Eocene phosphorites of the Metlaoui Group in Tunisia are a world-class phosphate resource. We review the characteristics of phosphorites deposited in three areas: the Northern Basins; Eastern Basins; and Gafsa-Metlaoui Basin. Comprehensive new bulk rock elemental data are presented, together with complementary mineralogical and mineral chemical results. Carbonate fluorapatite (francolite) constitutes the dominant mineral phase in the deposits. Phosphorite samples are enriched in Cd, Sr, U, rare-earth elements and Y, together with environmentally diagnostic trace elements that provide detrital (Cr, Zr), productivity (Cu, Ni, Zn) and redox (Mo, V) proxies. Suboxic bottom-water conditions predominated, with suboxic to anoxic porewaters accompanying francolite precipitation. Phosphorite deposition occurred under increasingly arid climate conditions, accompanying global Paleocene-Eocene warming. The Northern Basins show the strongest Tethys Ocean influence, with surface seawater rare-earth element signatures consistently developed in the phosphorites. Bed-scale compositional variation indicates relatively unstable environmental conditions and episodes of sediment redeposition, with varying detrital supply and a relatively wet local climate. Glauconitic facies in the Northern Basins and the more isolated evaporite-associated phosphorites in the dryer Eastern Basins display the greatest diagenetic influences. The phosphorite - organic-rich marl - diatom-bearing porcelanite facies association in the Gafsa-Metlaoui Basin represents the classic coastal upwelling trinity. Modified Tethyan waters occurred within the Basin during phosphorite deposition, with decreasing marine productivity from NW to SE evidenced by systematically falling enrichment factors for Cu, Ni, Cd and Zn in the phosphorites. Productivity declined in concert with increasing basin isolation during the deposition of the commercial phosphorite beds in the latest Paleocene to earliest

  2. Upper Cretaceous (Campanian) phosphorites in Jordan: implications for the formation of a south Tethyan phosphorite giant

    NASA Astrophysics Data System (ADS)

    Pufahl, Peir K.; Grimm, Kurt A.; Abed, Abdulkader M.; Sadaqah, Rushdi M. Y.

    2003-10-01

    A record of sedimentary, authigenic, and biological processes are preserved within the Upper Cretaceous (Campanian) Alhisa Phosphorite Formation (AP) in central and northern Jordan. The AP formed near the eastern extremity of the south Tethyan Phosphorite Province (STPP), a carbonate-dominated Upper Cretaceous to Eocene "phosphorite giant" that extends from Colombia, North Africa to the Middle East. Multidisciplinary research of the AP and associated cherts, chalks, and oyster buildups indicate that phosphatic strata formed on a highly productive, storm-dominated, east-west trending epeiric platform along the south Tethyan margin. The onset of phosphogenesis and the accumulation of economic phosphorite coincided with a rise in relative sea level that onlapped peritidal carbonates of the Ajlun Group. Pristine phosphates are associated with well-developed micrite concretionary horizons and contain abundant non-keeled spiral planktic foraminifera and a low diversity benthic assemblage of Buliminacean foraminifera, suggesting that pristine phosphates are a condensed facies and phosphogenesis was stimulated by the effects of a highly productive surface ocean and the suboxic diagenesis of sedimentary organic matter. The bulk sediment composition and absence of Fe-bearing authigenic phases such as glauconite, pyrite (including pyrite molds), siderite, and goethite within pristine phosphates suggests that deposition and authigenesis occurred under conditions of detrital starvation and that "iron-pumping" played a minimal role in phosphogenesis. Authigenic precipitation of phosphate occurred in a broad array of sedimentary environments—herein termed a "phosphorite nursery"—that spanned the entire platform. This is a non-uniformitarian phenomenon reflecting precipitation of sedimentary apatite across a wide depositional spectrum in a variety of depositional settings, wherever the conditions were suitable for phosphogenesis. Sedimentologic data indicate that pristine

  3. Marine phosphorites as potential resources for heavy rare earth elements and yttrium

    USGS Publications Warehouse

    Hein, James; Koschinsky, Andrea; Mikesell, Mariah; Mizell, Kira; Glenn, Craig R.; Wood, Ray

    2016-01-01

    Marine phosphorites are known to concentrate rare earth elements and yttrium (REY) during early diagenetic formation. Much of the REY data available are decades old and incomplete, and there has not been a systematic study of REY distributions in marine phosphorite deposits that formed over a range of oceanic environments. Consequently, we initiated this study to determine if marine phosphorite deposits found in the global ocean host REY concentrations of high enough grade to be of economic interest. This paper addresses continental-margin (CM) and open-ocean seamount phosphorites. All 75 samples analyzed are composed predominantly of carbonate fluorapatite and minor detrital and authigenic minerals. CM phosphorites have low total REY contents (mean 161 ppm) and high heavy REY (HREY) complements (mean 49%), while seamount phosphorites have 4–6 times higher individual REY contents (except for Ce, which is subequal; mean ΣREY 727 ppm), and very high HREY complements (mean 60%). The predominant causes of higher concentrations and larger HREY complements in seamount phosphorites compared to CM phosphorites are age, changes in seawater REY concentrations over time, water depth of formation, changes in pH and complexing ligands, and differences in organic carbon content in the depositional environments. Potential ore deposits with high HREY complements, like the marine phosphorites analyzed here, could help supply the HREY needed for high-tech and green-tech applications without creating an oversupply of the LREY.

  4. Depositional setting and geochemistry of phosphorites and metalliferous black shales in the Carboniferous-Permian Lisburne Group, Northern Alaska

    USGS Publications Warehouse

    Dumoulin, Julie A.; Slack, John F.; Whalen, Michael T.; Harris, Anita G.

    2011-01-01

    Phosphatic rocks are distributed widely in the Lisburne Group, a mainly Carboniferous carbonate succession that occurs throughout northern Alaska. New sedimentologic, paleontologic, and geochemical data presented here constrain the geographic and stratigraphic extent of these strata and their depositional and paleogeographic settings. Our findings support models that propose very high oxygen contents of the Permo-Carboniferous atmosphere and oceans, and those that suggest enhanced phosphogenesis in iron-limited sediments; our data also have implications for Carboniferous paleogeography of the Arctic. Lisburne Group phosphorites range from granular to nodular, are interbedded with black shale and lime mudstone rich in radiolarians and sponge spicules, and accumulated primarily in suboxic outer- to middle-ramp environments. Age constraints from conodonts, foraminifers, and goniatite cephalopods indicate that most are middle Late Mississippian (early Chesterian; early late Visean). Phosphorites form 2- to 40-cm-thick beds of sand- to pebble-sized phosphatic peloids, coated grains, and (or) bioclasts cemented by carbonate, silica, or phosphate that occur through an interval =12 m thick. High gamma-ray response through this interval suggests strongly condensed facies related to sediment starvation and development of phosphatic hardgrounds. Phosphorite textures, such as unconformity-bounded coated grains, record multiple episodes of phosphogenesis and sedimentary reworking. Sharp bed bases and local grading indicate considerable redeposition of phosphatic material into deeper water by storms and (or) gravity flows. Lisburne Group phosphorites contain up to 37 weight percent P2O5, 7.6 weight percent F, 1,030 ppm Y, 517 ppm La, and 166 ppm U. Shale-normalized rare earth element (REE) plots show uniformly large negative Ce anomalies Ce/Ce*=0.11 + or - 0.03) that are interpreted to reflect phosphate deposition in seawater that was greatly depleted in Ce due to increased

  5. Campanian-Maastrichtian phosphorites of Iraq

    NASA Astrophysics Data System (ADS)

    Al-Bassam, K. S.; Al-Dahan, A. A.; Jamil, A. K.

    1983-08-01

    Bedded marine sedimentary phosphate rocks of Campanian-Maastrichtian age are exposed in the Western Desert of Iraq, forming part of the Tethyan phosphate province. The studied phosphorites are found in three horizons within carbonate rocks; they are mostly pelletal in texture, associated with bone fragments and detrital quartz grains, and cemented by calcite or chert. The mineralogy of the phosphate is dominated by carbonate-fluorapatite. The phosphate and the associated carbonate rocks are relatively enriched with Cr, Ni, Cu, Zn, V, and organic matter. The apatite is enriched with isotopically light carbon and heavy sulfur. The mode of phosphorite formation seems to have included syngenetic deposition of phosphate under reducing, slightly alkaline conditions in shallow marine environment. Decomposition of organic phosphatic remnants appear to have been the local source of phosphorus enrichment. However, the major tectonic and paleogeographic development of the Tethys Sea during Upper Cretaceous have probably played an important role in providing suitable setting for large scale formation of phosphorite.

  6. Phosphorite-hosted zinc and lead mineralization in the Sekarna deposit (Central Tunisia)

    USGS Publications Warehouse

    Garnit, Hechmi; Bouhel, Salah; Barca, Donatella; Johnson, Craig A.; Chtara, Chaker

    2012-01-01

    The Sekarna Zn–Pb deposit is located in Central Tunisia at the northeastern edge of the Cenozoic Rohia graben. Mineralization comprises two major ore types: (1) disseminated Zn–Pb sulfides that occur as lenses in sedimentary phosphorite layers and (2) cavity-filling zinc oxides (calamine-type ores) that crosscut Late Cretaceous and Early Eocene limestone. We studied Zn sulfide mineralization in the Saint Pierre ore body, which is hosted in a 5-m-thick sedimentary phosphorite unit of Early Eocene age. The sulfide mineralization occurs as replacements of carbonate cement in phosphorite. The ores comprise stratiform lenses rich in sphalerite with minor galena, Fe sulfides, and earlier diagenetic barite. Laser ablation–inductively coupled plasma mass spectrometry analyses of sphalerite and galena show a wide range of minor element contents with significant enrichment of cadmium in both sphalerite (6,000–20,000 ppm) and galena (12–189 ppm). The minor element enrichments likely reflect the influence of the immediate organic-rich host rocks. Fluid inclusions in sphalerite give homogenization temperatures of 80–130°C. The final ice melting temperatures range from −22°C to −11°C, which correspond to salinities of 15–24 wt.% NaCl eq. and suggest a basinal brine origin for the fluids. Sulfur isotope analyses show uniformly negative values for sphalerite (−11.2‰ to −9.3‰) and galena (−16‰ to −12.3‰). The δ34S of barite, which averages 25.1‰, is 4‰ higher than the value for Eocene seawater sulfate. The sulfur isotopic compositions are inferred to reflect sulfur derivation through bacterial reduction of contemporaneous seawater sulfate, possibly in restricted basins where organic matter was abundant. The Pb isotopes suggest an upper crustal lead source.

  7. Phosphorite-hosted zinc and lead mineralization in the Sekarna deposit (Central Tunisia)

    NASA Astrophysics Data System (ADS)

    Garnit, Hechmi; Bouhlel, Salah; Barca, Donatella; Johnson, Craig A.; Chtara, Chaker

    2012-06-01

    The Sekarna Zn-Pb deposit is located in Central Tunisia at the northeastern edge of the Cenozoic Rohia graben. Mineralization comprises two major ore types: (1) disseminated Zn-Pb sulfides that occur as lenses in sedimentary phosphorite layers and (2) cavity-filling zinc oxides (calamine-type ores) that crosscut Late Cretaceous and Early Eocene limestone. We studied Zn sulfide mineralization in the Saint Pierre ore body, which is hosted in a 5-m-thick sedimentary phosphorite unit of Early Eocene age. The sulfide mineralization occurs as replacements of carbonate cement in phosphorite. The ores comprise stratiform lenses rich in sphalerite with minor galena, Fe sulfides, and earlier diagenetic barite. Laser ablation-inductively coupled plasma mass spectrometry analyses of sphalerite and galena show a wide range of minor element contents with significant enrichment of cadmium in both sphalerite (6,000-20,000 ppm) and galena (12-189 ppm). The minor element enrichments likely reflect the influence of the immediate organic-rich host rocks. Fluid inclusions in sphalerite give homogenization temperatures of 80-130°C. The final ice melting temperatures range from -22°C to -11°C, which correspond to salinities of 15-24 wt.% NaCl eq. and suggest a basinal brine origin for the fluids. Sulfur isotope analyses show uniformly negative values for sphalerite (-11.2‰ to -9.3‰) and galena (-16‰ to -12.3‰). The δ34S of barite, which averages 25.1‰, is 4‰ higher than the value for Eocene seawater sulfate. The sulfur isotopic compositions are inferred to reflect sulfur derivation through bacterial reduction of contemporaneous seawater sulfate, possibly in restricted basins where organic matter was abundant. The Pb isotopes suggest an upper crustal lead source.

  8. Composition and origin of Early Cambrian Tiantaishan phosphorite-Mn carbonate ores, Shaanxi Province, China

    USGS Publications Warehouse

    Hein, J.R.; Fan, D.; Ye, J.; Liu, T.; Yeh, H.-W.

    1999-01-01

    The Tiantaishan phosphorite-Mn carbonate ores occur in the Early Cambrian Tananpo Formation in complexly folded and faulted rocks located in southern Shaanxi Province. About 65 x 106 tonnes of 17% P2O5 ore reserves exist and Mn-ore reserves are about 8.3 x 106 tonnes of +18% Mn. The stratigraphic sequence in ascending order consists of black phyllite, black to gray phosphorite ore, black phyllite, rhodochrostone ore, Mn mixed-carbonates, and dolostone. Data are presented from microprobe mineral chemistry, whole-rock chemistry, stable isotopes of carbonates, X-ray mineralogy, petrographic and SEM observations, and statistical analysis of chemical data. The dominant ore-forming minerals are hydroxy- and carbonate fluorapatite and Ca rhodochrosite, with Mg kutnahorite and dolomite comprising the Mn mixed-carbonate section. Pyrite occurs in all rock types and alabandite (MnS) occurs throughout the rhodochrostone section. The mean P2O5 content of phosphorite is 31% and argillaceous phosphorite is 16%, while the mean MnO content of rhodochrostone ore is 37%. Phosphorite ores are massive, spheroidal, laminated, and banded, while rhodochrostone ores have oolitic, spheroidal, and granular fabrics. The most distinguishing characteristics of the ores are high total organic carbon (TOC) contents (mean 8.4%) in the phosphorite and high P2O5 contents (mean 2.7%) in the rhodochrostone ore. The atypically high TOC contents in the Tiantaishan phosphorite probably result from very strong productivity leading to high sedimentation rates accompanied by weak reworking of sediments; poor utilization of the organic matter by bacteria; and/or partial replacement of bacterial or algal mats by the apatite. The depositional setting of the ores was the margin of an epicontinental seaway created as a direct consequence of global processes that included break-up of a supercontinent, formation of narrow seaways, creation of extensive continental shelves, overturn of stagnant, metal-rich deep

  9. Microbial Communities Associated with Phosphorite-bearing Sediments

    NASA Astrophysics Data System (ADS)

    Zoss, R.; Bailey, J.; Flood, B.; Jones, D. S.

    2016-12-01

    Phosphorus is a limiting nutrient in the environment and is an important component of many biological molecules. Calcium phosphate mineral deposits known as phosphorites, are also the primary source of P for agriculture. Understanding phosphorite formation may improve management of P resources. However, the processes that mediate calcium phosphate mineral precipitation in certain marine pore waters remain poorly understood. Phosphogenesis occurs in sediments beneath some oceanic upwelling zones that harbor polyphosphate-accumulating giant sulfur bacteria (GSB). These bacteria may concentrate phosphate in sediment pore waters - creating supersaturated conditions with respect to apatite. However, the relationship between microbes and phosphogenesis is not fully resolved. To further study this relationship, we examined microbial communities from two sources: sediment cores recovered from the shelf of the Benguela region, and DNA extracted from washed phosphorites recovered from those same sediments. We used itag and clone library sequencing of the 16S rRNA gene to examine the microbial communities and their relationship with the environment. We found that many of our sediments shared large numbers of phylotypes with one another, and that the same metabolic guilds were represented at localities across the shelf. Sulfur-reducing bacteria and sulfur-oxidizing bacteria were abundant in our datasets. Phylotypes that are known to carry out nitrification and/or anammox (anaerobic ammonia oxidation) were also well-represented. Our phosphorite extraction, however, contained a distinct microbial community from those observed in the modern sediments. We observed both an enrichment of certain common microbial classes and a complete absence of others. These results could represent an ancient microbial assemblage that was present when the apatite precipitated. While these taxa may or may not have contributed to apatite precipitation, several groups represented in the phosphorite

  10. Domestic phosphate deposits

    USGS Publications Warehouse

    McKelvey, V.E.; Cathcart, J.B.; Altschuler, Z.S.; Swanson, R.W.; Lutz, Katherine

    1953-01-01

    Most of the worlds phosphate deposits can be grouped into six types: 1) igneous apatite deposits; 2) marine phosphorites; 3) residual phosphorites; 4) river pebble deposits; 5) phosphatized rock; and 6) guano. The igneous apatites and marine phosphorites form deposits measurable in millions or billions of tons; the residual deposits are measurable in thousands or millions; and the other types generally only in thousands of tons. Igneous apatite deposits have been mined on a small scale in New York, New Jersey, and Virginia. Marine phosphorites have been mined in Montana, Idaho, Utah, Wyoming, Arkansas, Tennessee, North Carolina, South Carolina, Georgia, and Florida. Residual phosphorites have been mined in Tennessee, Pennsylvania, and Florida. River pebble has been produced in South Carolina and Florida; phosphatized rock in Tennessee and Florida; and guano in New Mexico and Texas. Present production is limited almost entirely to Florida, Tennessee, Montana, Idaho, and Wyoming. Incomplete but recently partly revised estimates indicate the presence of about 5 billion tons of phosphate deposits in the United States that is minable under present economic conditions. Deposits too lean in quality or thickness to compete with those in the western and southeastern fields probably contain tens of billions of tons.

  11. Seawater Phosphorites of the Seamount, Southwestern Pacific

    NASA Astrophysics Data System (ADS)

    Yoo, C.; Moon, J.; Kim, J.; Kim, K.; Lee, K.

    2002-12-01

    Phosphatized carbonate rocks associated with ferromanganese crusts (Fe-Mn crust) were investigated for better understanding of diagenetic evolution of the seamount (one of the Margellan Seamount Trail), southwestern Pacific. Three stages of phosphatization are inferred on the basis of paragenetic relation with Fe-Mn crusts, which are divided into four layers by their textures; 1) layer 1, massive, columnar growth structures with some porosity, 2) layer 2, porous, digitate growth structures with brown Fe-oxide filling, 3) layer 3, digitate and ovoidal growth structures with carbonate sediments filling, 4) layer 4, massive, parallel to undulatory laminated textures. Early phosphatization (phosphorite I) occurred before the formation of the oldest layer 4 crust. Foraminiferal-nannofossil limestones and shallow-water bioclastic limestones, encrusted by layer 4 crusts, are replaced by phosphorite I. Strontium isotope ratios (0.70743 to 0.70766) indicate that this phosphorite is formed at Late Cretaceous (85.2 to 73.5 Ma). Oxygen isotope values (-0.6 to 0.1% PDB) and shale-normalized REE pattern suggest that phosphorite I was formed in normal seawater. Phosphorite I appears as subhedral to euhedral, prismatic hexagonal crystallites approximately less than 5 æm in length. The second phosphorite (phosphorite II) is formed during the cessation of layer 4 crusts. Foraminiferal-nannofossil limestones filling the fractures developed within layer 4 crust are phosphatized during this episode. Age of phospatization II is defined as Late Eocene to Early Oligocene (36.5 to 31.6 Ma) from strontium isotope ratios (0.70777 to 0.70793). Oxygen isotope values (-2.9 to 2.9% PDB) and shale-normalized REE pattern of phosphorite II also suggest normal seawater origin. Phosphorite II replaced carbonate grain appears as anhedral, submicron-sized crystallites, whereas euhedral, prismatic hexagonal crystallites are filling the open space. Global climatic transition from a nonglacial to glacial

  12. Uranium, Thorium and some other trace elements in phosphorites from different provenances

    NASA Astrophysics Data System (ADS)

    Bech, J.; Reverter, F.; Tume, P.; Roca, N.; Suarez, E.; Sepúlveda, G.; Sokolovska, M.

    2012-04-01

    Data on the trace element composition of phosphorites is scarce. Some of them may be harmful at certain concentrations. Special concern is given to the radionuclides U and Th and some other heavy metals such as: Co, Cr, Cu, Ni and V. Phosphorites of different origins can vary significantly in the trace element concentrations. 37 samples of phosphorites from 16 deposits were analyzed for Uranium, Thorium and five potential toxic elements (Co, Cr, Cu, Ni and V) as well as 26 samples of data gathered from the literature. In total 63 samples of phosphorites from 20 deposits of 19 countries were studied: Algeria, Australia, Brazil, Burkina Faso, Chile, Colombia, Egypt, India, Israel, Mongolia, Morocco, New Zealand, Peru, Senegal, Syria, Togo, Tunisia, USA and Venezuela. Aqua regia extracts were used to estimate the "pseudototal" values, following standard procedures (ISO 11466, 2002) and measured by ICP-MS. The median concentrations (mgkg-1) obtained were: U 53 (range 0.20-177), Th 4.05 (range 1-49), Co 4 (range 0.5-159), Cr 100 (range 15-1000), Cu 20 (range 5-213), Ni 21 (range 3-850) and V 70.05 (range 20-591). As 120 mgkg-1 of U concentration of phosphorites is the value considered to be useful as a source of nuclear fuel, we now indicate the deposits with values higher than 120 mgkg-1: Khouribga KIISB (Morocco) 121, Khouribga KIISL (Morocco) 123, Champ mines (Idaho, USA) 131, Noralyn (Central Florida, USA) 138, Bone Valley (Florida, USA) 140, Boucraa BGB (Morocco) 141, Boucraa BGC (Morocco) 152, Negev (Israel) 172 and Chatam Rise (New Zealand) 177. The highest Th concentration found was 49 mgkg-1 at Bijawar Group (India). Uranium shows significant positive correlations with V (r = 0.41) and Cr (r = 0.30), and significant negative correlations with Co (r= -0.47). Other positive correlations are Cr with Cu (r=0.58), Cr with V (r=0.52) and Cr with Ni (r=0.51). Cu correlates positively with Ni (r=0.84) and with V (r=0.63). Ni correlates positively with V (r=0.72).

  13. Geochemistry of Late Cretaceous phosphorites in Egypt: Implication for their genesis and diagenesis

    NASA Astrophysics Data System (ADS)

    Baioumy, H. M.; Tada, R.; Gharaie, M. H. M.

    2007-09-01

    Phosphorite deposits in Egypt, known as the Duwi Formation, are a part of the Middle East to North Africa phosphogenic province of Late Cretaceous to Paleogene age. Phosphatic grains in these deposites are classified into phosphatic mudclasts and phosphatic bioclasts. Phosphatic bioclasts are subdivided into fish bone fragments and shark tooth fragments. All phosphatic grains are composed of francolite. Chemical mapping of the phosphatic grains using Electron Probe Microanalysis (EPMA) indicated that the phosphatic mudclasts are homogeneous in their chemical composition and no concentric texture nor chemical zoning are observed. Some of the bone fragments show Fe and S zoning. No significant difference in chemical composition is observed between the phosphatic mudclasts and bioclasts. Acid-insoluble residues of the phosphorites show lower values of the Chemical Index of Alteration (CIA) compared to the associated rocks. Structural CO 2 contents in the francolites range from 3.32% to 7.21% with an average of 5.3%. The δ13C PDB values range from -4.04‰ to -8.7‰, while the δ18O PDB values range from -4.3‰ to -10.3‰. The compositional homogeneity of the mudclasts, Fe and S zoning in some of the bone fragments and the difference in the Chemical Index of Alteration between the acid-insoluble residues of the phosphorites and the associated rocks suggest that the phosphatic grains in the Duwi Formation are derived from pre-existing authigenic phosphorites, which reworked and concentrated afterward. Negative δ13C values of structural CO 2 suggest that the CO 2 was derived from degradation of organic matter. Low δ18O values of structural CO 2 can be attributed to the influence of meteoric water. Higher CO 2, SO 3 and F contents compared to the recent authigenic phosphorites and negative δ13C and δ18O values of structural CO 2 indicate that diagenesis plays an important role in the modification of the chemical composition of phosphatic grains and that the

  14. Geochemistry and microprobe investigations of Abu Tartur REE-bearing phosphorite, Western Desert, Egypt

    NASA Astrophysics Data System (ADS)

    Awadalla, Gamal S.

    2010-07-01

    Phosphorites in Egypt occur in the Eastern Desert, the Nile Valley and the Western Desert at Abu Tartur area and present in Duwi Formation as a part of the Middle Eastern to North African phosphogenic province of Late Cretaceous to Paleogene age (Campanian-Maastrichtian). The Maghrabi-Liffiya phosphorite sector is considered as the most important phosphorite deposits in the Abu Tartur area due to its large reserve thickness and high-grade of lower phosphorite bed beside high content of REE. Back scattered electron (BSE) images show framboidal pyrite filling the pores of the phosphatic grains, suggesting diagenetic reducing conditions during phosphorites formation. Electron Probe Micro Analyzer (EPMA) chemical mapping was conducted to examine the variation and distributions of selected elements (P, F, La, Fe, Yb, Si, Ce, W, Eu, S, Ca, Y and Er) within the shark teeth, coprolites and bone fragments. In the teeth W, S, Fe are concentrated along the axis of the teeth, the bone fragments show high concentration of W, Yb, Er and Eu, whereas coprolites are nearly homogenous in composition contains S, Er with some Si as micro-inclusions. Fluorapatite is considered as main phosphate mineral whereas pyrite occurs as pore-filling within the phosphatic grains and cement materials. Maghrabi-Liffiya samples show a wide range in the P 2O 5 content, between 19.8 wt.% and 29.8 wt.% with an average of 24.6 wt.% and shows low U content ranging from 15 ppm to 34 ppm with an average of 22 ppm. The total REE content in nine samples representing the Maghrabi-Liffiya ranges from 519 to 1139 ppm with an average of about 879 ppm. The calculation of LREE (La-Gd) show indeed a marked enrichment relative to the HREE (Tb-Lu) where LREE/HREE ratio attains 8.4 indicating a strong fractionation between the LREE and HREE. Chondrite-normalized REE patterns of the studied phosphorite samples show a negative Eu anomaly.

  15. ATLAS of Microorganisms from Ancient Phosphorites of Khubsugul (Mongolia)

    NASA Technical Reports Server (NTRS)

    Zhengallo, Elena A.; Rozanov, Alexei Yu.; Ushatinskaya, Galina T.; Hoover, Richard B.; Gerasimenko, Ludmila M.; Ragozina, Alla L.

    2000-01-01

    A photographic atlas of scanning electron microscope (SEM) images of Cambrian (Tommotian) microfossils from the phosphorites of Khubsugul Mongolia is presented. SEM images of modern cyanobacteria and bacteria are provided for comparison. The importance of bacterial fossils and morphological biomarkers to astrobiology and the understanding of the origin of phosphorites is considered.

  16. 3D-Mapping of Dolomitized Structures in Lower Cambrian Phosphorites

    NASA Astrophysics Data System (ADS)

    Hippler, Dorothee; Stammeier, Jessica A.; Brunner, Roland; Rosc, Jördis; Franz, Gerhard; Dietzel, Martin

    2016-04-01

    Dolomitization is a widespread phenomenon in ancient sedimentary rocks, particularly close to the Precambrian-Cambrian boundary. Dolomite can form in synsedimentary or hydrothermal environments, preferentially via the replacement of solid carbonate precursor phases. Synsedimentary dolomite formation is often associated with microbial activity, such as bacterial sulfate reduction or methanogenesis. In this study, we investigate dolomitic phosphorites from the Lowermost Cambrian Tal Group, Mussoori Syncline, Lesser Himalaya, India, using micro-CT 3D-mapping, in order to unravel the complex diagenetic history of the rocks. The selected sample shows alternating layering of phosphatic mudstones and sparitic dolostone, in which brecciated layers of phosphorite or phosphatic mudstones are immersed in a dolomite-rich matrix. Lamination occurs on a sub-millimetre scale, with lamination sometimes wavy to crinkly. This fabric is interpreted as former microbial mats, providing the environment for early diagenetic phosphatization. Preliminary electron backscatter imaging with scanning microscopy revealed that dolomite crystals often occur in spherical to ellipsoidal structures, typically with a high porosity. This dolomite is associated with botryoidal apatite, organic matter and small amounts of calcite. Micro-CT 3D-mappings reveal that dolomite structures are cigar-shaped, elongated and up to 600 μm long. They are further arranged in a Mikado-like oriented framework spanning a layer thickness of a few millimetres. Analyses of ambient pore space, with similar elongated outlines and filled with organic matter, suggest a potential coherence of ambient pore space and shape of the dolomite structures. Allowing for other associated mineral phases, such as pyrite and silicates, and their spatial distribution, the present approach can be used to unravel distinct diagenetic reaction pathways, and might thus constrain the proxy potential of these Lower Cambrian dolomitic phosphorites

  17. Chemical composition of phosphorites of the Phosphoria Formation

    USGS Publications Warehouse

    Gulbrandsen, R.A.

    1966-01-01

    The chemical composition, both major and minor constituents, of 60 samples of phosphorite from the Phosphoria Formation was determined. Major constituents of the average phosphorite are, by weight per cent: SiO2, 11??9; Al2O3, 1??7; Fe2O3,1??1; MgO, 0??3; CaO, 44??0; Na2O, 0??6; K2O, 0??5; total H2O, 2??2; H2O-, 0??6; TiO2, 0??1; P2O5, 30??5; CO2, 2??2; SO3, 1??8; F, 3??1; organic matter, 2??1; and oil, 0??2. Uranium averages 0??009 per cent. The phosphate mineral is basically apatite, Ca5(PO4)3F, with small but significant and variable substitutions-Na, Sr, U and Th for Ca, and CO3 and SO4 for PO4. Rare metals not associated with apatite are associated principally with the organic-matter component of the rocks. This group includes As, Ag, Cd, Cr, Cu, Mo, Ni, Sb, Se, V and Zn. Chromium is the most abundant, having a modal abundance of 0??1 per cent and a maximum concentration of 0??3 per cent. The average phosphorite is composed of approximately 80 per cent apatite, 10 per cent quartz, 5 per cent muscovite-illite, 2 per cent organic matter, 1 per cent dolomite-calcite, 1 per cent iron oxide, and 1 per cent other components. It is texturally a medium-grained pellet phosphorite. ?? 1966.

  18. Eumetazoan fossils in terminal Proterozoic phosphorites?

    PubMed Central

    Xiao, Shuhai; Yuan, Xunlai; Knoll, Andrew H.

    2000-01-01

    Phosphatic sedimentary rocks preserve a record of early animal life different from and complementary to that provided by Ediacaran fossils in terminal Proterozoic sandstones and shales. Phosphorites of the Doushantuo Formation, South China, contain eggs, egg cases, and stereoblastulae that document animals of unspecified phylogenetic position; small fossils containing putative spicules may specifically record the presence of sponges. Microfossils recently interpreted as the preserved gastrulae of cnidarian and bilaterian metazoans can alternatively be interpreted as conventional algal cysts and/or egg cases modified by diagenetic processes known to have had a pervasive influence on Doushantuo phosphorites. Regardless of this interpretation, evidence for Doushantuo eumetazoans is provided by millimeter-scale tubes that display tabulation and apical budding characteristic of some Cnidaria, especially the extinct tabulates. Like some Ediacaran remains, these small, benthic, colonial fossils may represent stem-group eumetazoans or stem-group cnidarians that lived in the late Proterozoic ocean. PMID:11095754

  19. Ediacaran stromatolites and intertidal phosphorite of the Salitre Formation, Brazil: Phosphogenesis during the Neoproterozoic Oxygenation Event

    NASA Astrophysics Data System (ADS)

    Caird, R. A.; Pufahl, P. K.; Hiatt, E. E.; Abram, M. B.; Rocha, A. J. D.; Kyser, T. K.

    2017-04-01

    The Ediacaran Nova America and Gabriel members of the Salitre Formation are composed of limestone and economic phosphorite that accumulated on an unrimmed epeiric ramp along the margins of the Irecê Basin, Brazil. Deposition occurred during a marine transgression punctuated by higher-order fluctuations in relative sea-level that produced m-scale, shallowing-upward peritidal cycles. Cycles consist of six lithofacies rich in microbial sedimentary structures including subtidal, cross-stratified grainstones and hemispheroidal columnar stromatolite reefs overlain by intertidal flat sediments indicative of decreasing accommodation. Phosphorite is restricted to the paleocoast where digitate stromatolite biostromes colonized tidal flats. Phosphorite accumulation is interpreted to have been associated with biostromes because photosynthetic oxygen production created a redox gradient beneath the seafloor that phosphogenic chemosynthetic bacteria exploited. The concentration of francolite or sedimentary apatite in microbial laminae suggests these bacteria actively stored, released, and concentrated phosphate to promote in situ precipitation. The sealing effect of interbedded, fine-grained tidal deposits was also critical for maintaining the high levels of pore water phosphate required. The absence of francolite in subtidal columnar stromatolite reefs implies phosphogenesis was prevented in deeper, more energetic environments because wave pumping of oxygenated seawater through reefs surrounded by constantly moving grainy sediment promoted the recycling of P directly back to the water column. The Salitre Formation has a complex paragenesis, including hydrothermal alteration that produced Mississippi Valley-type Pb-Zn mineralization. δ18O values of Nova America member dolomites range from - 10.2‰ to - 0.5‰ (mean = - 3.9‰) and δ13C ranges from - 9.2‰ to + 10.0‰ (mean = + 2.8‰). Samples contain varying proportions of low-Mg calcite and saddle dolomite. δ18O values

  20. Rare earth elements in sedimentary phosphate deposits: Solution to the global REE crisis?

    USGS Publications Warehouse

    Emsbo, Poul; McLaughlin, Patrick I.; Breit, George N.; du Bray, Edward A.; Koenig, Alan E.

    2015-01-01

    The critical role of rare earth elements (REEs), particularly heavy REEs (HREEs), in high-tech industries has created a surge in demand that is quickly outstripping known global supply and has triggered a worldwide scramble to discover new sources. The chemical analysis of 23 sedimentary phosphate deposits (phosphorites) in the United States demonstrates that they are significantly enriched in REEs. Leaching experiments using dilute H2SO4 and HCl, extracted nearly 100% of their total REE content and show that the extraction of REEs from phosphorites is not subject to the many technological and environmental challenges that vex the exploitation of many identified REE deposits. Our data suggest that phosphate rock currently mined in the United States has the potential to produce a significant proportion of the world's REE demand as a byproduct. Importantly, the size and concentration of HREEs in some unmined phosphorites dwarf the world's richest REE deposits. Secular variation in phosphate REE contents identifies geologic time periods favorable for the formation of currently unrecognized high-REE phosphates. The extraordinary endowment, combined with the ease of REE extraction, indicates that such phosphorites might be considered as a primary source of REEs with the potential to resolve the global REE (particularly for HREE) supply shortage.

  1. Petro-mineralogical Studies of the Paleoproterozoic Phosphorites in the Sonrai basin, Lalitpur District, Uttar Pradesh, India

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

    Dar, Shamim A., E-mail: sjshamim@gmail.com; Khan, K. F.; Khan, Saif A.

    2015-09-15

    The Paleoproterozoic phosphorites constitute an economically significant component of the Sonrai basin of Lalitpur district. These are associated with ferruginous shale, ironstone, limestone and quartz breccia. Petro-mineralogical studies of samples of the phosphorites, using X-ray diffractometry and scanning electron microscopy, reveal that the collophane (carbonate-fluorapatite) is the dominant phosphate mineral. Calcite, dolomite, quartz, mica and haematite are the dominant gangue constituents. The phosphate minerals occur as oolites mutually replaced by carbonate and silica. The presence of iron oxides has been found in most of the thin sections. There is meagre evidence of organic matter in the form of filaments ofmore » microbial phosphate laminae in the samples of phosphorite. The mineral assemblages, their texture and various forms in these phosphorites may be due to some environmental vicissitudes followed by replacement processes and biogenic activities.« less

  2. Origin of Cretaceous phosphorites from the onshore of Tamil Nadu, India

    NASA Astrophysics Data System (ADS)

    Purnachandra Rao, V.; Kessarkar, Pratima M.; Nagendra, R.; Babu, E. V. S. S. K.

    2007-12-01

    Cretaceous phosphorites from the onshore of Tamil Nadu have been investigated for their origin and compared with those in the offshore. Cretaceous phosphorites occur as light brown to yellowish brown or white nodules in Karai Shale of the Uttatur Group in the onshore Cauvery basin. Nodules exhibit phosphatic nucleus encrusted by a chalky shell of carbonate. The nucleus of the nodules consists of light and dark coloured laminae, phosphate peloids/coated grains and detrital particles interspersed between the laminae. Scanning electron microscope (SEM) studies reveal trapping and binding activity of microbial filaments. A mat structure with linearly arranged microbial filaments and hollow, cell-based coccoid cyanobacterial mat are present. Nodules contain abundant carbonate fluorapatite, followed by minor calcite, quartz and feldspar. The P2O5 content of the phosphorites ranges from 18 to 26%. The CaO/P2O5, Sr and F contents are higher than that of pure carbonate fluorapatite. Concentrations of Si, Al, K, Fe, and Ti are low. We suggest that the nuclei of the nodules represent phosphate clasts related to phosphate stromatolites formed at intertidal conditions. At high energy levels the microbial mats were disintegrated into phosphate clasts, coated with carbonate and then reworked into Karai Shale. On the other hand, Quaternary phosphorites occur as irregular to rounded, grey coloured phosphate clasts at water depths between 180 and 320m on the continental shelf of Tamil Nadu. They exhibit grain-supported texture. Despite Quaternary in age, they also resemble phosphate stromatolites of intertidal origin and reworked as phosphate clasts onto the shelf margin depressions. Benthic microbial mats probably supplied high phosphorus to the sediments. Availability of excess phosphorus seems to be a pre-requisite for the formation of phosphate stromatolites.

  3. Paleoclimatological change in the Late Neoproterozoic: Evidence from oxygen isotopes of phosphorite in Yangtze Platform, China

    NASA Astrophysics Data System (ADS)

    Ling, H.-F.; Jiang, S.-Y.; Feng, H.-Z.; Chen, J.-H.; Chen, Y.-Q.; Yang, J.-H.

    2003-04-01

    section. It is suggested that the phosphorite studied preserved primary oxygen isotopes, whereas d18Odolo values of the dolomite were altered by diagenesis. Potential causes for the overall increase trend of d18Ophos include increase in seawater d18O values and decrease in temperature. During the time span of about 10 ~ 30 Ma for the section deposition when no glaciation occurred, it seems not completely in reality to attribute the variation of more than 4‰ of d18O values to seawater change alone. To cause ~4.3‰ variation of d18Ophos, temperature would decrease about 15-20˚C, which is possible to happen in the Earth history (Lecuyer and Allemand, 2002). The following lines of evidence also support this view. The studied phosphorites were deposited after thaw of the Snowball Earth. During the Snowball Earth period, continental weathering was in minimum due to little precipitation. This, together with existence of volcanic CO2 emitting through the snowball, CO2 accumulated in the atmosphere up to very high level and thus the temperature would be very high soon after thaw of the Snowball Earth. This, combined with more precipitation, would cause progressive weathering. Enhanced weathering of continental rocks would draw down the CO2 of atmosphere and in turn cause cooling, which is consistent with temperature lowering of the period. Increase trend of Pb/Th ratio during the period is in good agreement with enhanced weathering. Pb and Th are both highly particle reactive elements in the ocean. However, their geochemical behaviors in weathering processes are potentially different. Pb is mainly contained in feldspar while Th is mainly hosted in accessory minerals such as monazite. During enhanced weathering processes feldspar can be altered and release Pb whereas monazite would usually survive. Therefore Pb/Th ratio in hydrogenic sediments would be an indicator of weathering intensity. Enhanced weathering would also provide more nutrition elements to ocean, resulting in

  4. Nanoscale petrographic and geochemical insights on the origin of the Palaeoproterozoic stromatolitic phosphorites from Aravalli Supergroup, India.

    PubMed

    Papineau, D; De Gregorio, B; Fearn, S; Kilcoyne, D; McMahon, G; Purohit, R; Fogel, M

    2016-01-01

    Stromatolites composed of apatite occur in post-Lomagundi-Jatuli successions (late Palaeoproterozoic) and suggest the emergence of novel types of biomineralization at that time. The microscopic and nanoscopic petrology of organic matter in stromatolitic phosphorites might provide insights into the suite of diagenetic processes that formed these types of stromatolites. Correlated geochemical micro-analyses of the organic matter could also yield molecular, elemental and isotopic compositions and thus insights into the role of specific micro-organisms among these communities. Here, we report on the occurrence of nanoscopic disseminated organic matter in the Palaeoproterozoic stromatolitic phosphorite from the Aravalli Supergroup of north-west India. Organic petrography by micro-Raman and Transmission Electron Microscopy demonstrates syngeneity of the organic matter. Total organic carbon contents of these stromatolitic phosphorite columns are between 0.05 and 3.0 wt% and have a large range of δ(13) Corg values with an average of -18.5‰ (1σ = 4.5‰). δ(15) N values of decarbonated rock powders are between -1.2 and +2.7‰. These isotopic compositions point to the important role of biological N2 -fixation and CO2 -fixation by the pentose phosphate pathway consistent with a population of cyanobacteria. Microscopic spheroidal grains of apatite (MSGA) occur in association with calcite microspar in microbial mats from stromatolite columns and with chert in the core of diagenetic apatite rosettes. Organic matter extracted from the stromatolitic phosphorites contains a range of molecular functional group (e.g. carboxylic acid, alcohol, and aliphatic hydrocarbons) as well as nitrile and nitro groups as determined from C- and N-XANES spectra. The presence of organic nitrogen was independently confirmed by a CN(-) peak detected by ToF-SIMS. Nanoscale petrography and geochemistry allow for a refinement of the formation model for the accretion and phototrophic growth of

  5. Nanometer-scale characterization of exceptionally preserved bacterial fossils in Paleocene phosphorites from Ouled Abdoun (Morocco).

    PubMed

    Cosmidis, J; Benzerara, K; Gheerbrant, E; Estève, I; Bouya, B; Amaghzaz, M

    2013-03-01

    Micrometer-sized spherical and rod-shaped forms have been reported in many phosphorites and often interpreted as microbes fossilized by apatite, based on their morphologic resemblance with modern bacteria inferred by scanning electron microscopy (SEM) observations. This interpretation supports models involving bacteria in the formation of phosphorites. Here, we studied a phosphatic coprolite of Paleocene age originating from the Ouled Abdoun phosphate basin (Morocco) down to the nanometer-scale using focused ion beam milling, transmission electron microscopy (TEM), and scanning transmission x-ray microscopy (STXM) coupled with x-ray absorption near-edge structure spectroscopy (XANES). The coprolite, exclusively composed of francolite (a carbonate-fluroapatite), is formed by the accumulation of spherical objects, delimited by a thin envelope, and whose apparent diameters are between 0.5 and 3 μm. The envelope of the spheres is composed of a continuous crown dense to electrons, which measures 20-40 nm in thickness. It is surrounded by two thinner layers that are more porous and transparent to electrons and enriched in organic carbon. The observed spherical objects are very similar with bacteria encrusting in hydroxyapatite as observed in laboratory experiments. We suggest that they are Gram-negative bacteria fossilized by francolite, the precipitation of which started within the periplasm of the cells. We discuss the role of bacteria in the fossilization mechanism and propose that they could have played an active role in the formation of francolite. This study shows that ancient phosphorites can contain fossil biological subcellular structures as fine as a bacterial periplasm. Moreover, we demonstrate that while morphological information provided by SEM analyses is valuable, the use of additional nanoscale analyses is a powerful approach to help inferring the biogenicity of biomorphs found in phosphorites. A more systematic use of this approach could considerably

  6. A Geochemical Analysis of Rare Earth Elements Associated with Significant Phosphate Deposits of West-Central Florida

    NASA Astrophysics Data System (ADS)

    Turner, K. M.; Owens, J. D.

    2017-12-01

    Rare earth elements (REEs) such as the lanthanide series as well as yttrium, uranium, and thorium are an important industrial resource for expanding technological sectors; therefore, demand and production will continue to increase. Increased market prices resulting in decreased demand has led to new exploration for REE mineral resources in North America. Phosphorite deposits are being investigated as a possible supply but the overall concentrations, depositional environments, and ages are relatively unexplored. Phosphorite is commonly associated with ocean floor sediment deposition and upwelling; however, it may also form in estuarine and supratidal zones with low wave activity, present along Florida's west coast. Interestingly, it seems that major ancient phosphorite deposits are often, if not always, associated with major icehouse conditions (widespread glaciations) and rarely observed during greenhouse conditions. By analyzing a set of sonic drill cores, spatiotemporal REE concentrations can be better constrained for a wide-age range of the Miocene-Pliocene aged Bone Valley Member of the Peace River Formation, the largest North American phosphate deposit. We present concentrations from a depth-transect of samples collected in West-Central Florida, showing the phosphatic sands and silts of the area are highly enriched sedimentary archives for REE, yielding concentrations up to 200 ppm for some REE. The weathering and transport of igneous and metamorphic minerals from the southern Appalachians to the Florida coast where a series of winnowing events occurred may explain the enrichment seen by our data. Sediment cores showing well-rounded quartz sands, dolomitic silts, teeth, bones, and marine fossils commonly found in a near shore depositional environment support this hypothesis. Previous analysis of phosphate grains, teeth, bones, and bulk sediment indicate REE are not associated with and/or sourcing from biogenic components, but rather entering the lattice

  7. Phosphatized algal-bacterial assemblages in Late Cretaceous phosphorites of the Voronezh Anteclise

    NASA Astrophysics Data System (ADS)

    Maleonkina, Svetlana Y.

    2003-01-01

    Late Cretaceous phosphogenesis of the Voronezh Anteclise has occurred during Cenomanian and Early Campanian. SEM studies show the presence of phosphatized algal-bacterial assemblages both in Cenomanian and Campanian phosphorites. In some Cenomanian nodular phosphorite samples revealed empty tubes 1 - 5 microns in diameter, which are most likely trichomes of cyanobacterial filaments. Other samples contained accumulations of spheres 0,5-3 microns, similar to coccoidal bacteria. Complicated tubular forms with variable diameter 2 - 5 microns occur on surface of some quartz grains in nodules. They are probably pseudomorphs after algae. We found similar formations in the Campanian phosphate grains. Frequently, grain represents a cyanobacterial mat, which is sometimes concentrically coated by phosphatic films. The films of some grains retain the primary structure, their concentric layers are formed by pseudomorphs after different bacterial types and obviously they represent oncolite. In other cases, the primary structure is unobservable because of recrystallization process erases them. Occasionally, the central part retains the coccoidal structure and the recrystallization affects only films. Besides the core of such oncolite can be represented not only by phosphatic grain, but also by grains of other minerals, such as quartz, glauconite and heavy minerals, which serve as a substrate for cyanobacterial colonies. Bacteria also could settle on cavity surfaces and interiors frames of sponge fragments, teeth and bones.

  8. Late Cretaceous to Miocene phosphatic sediments in the Georges Bank Basin, U.S. North Atlantic outer continental shelf

    USGS Publications Warehouse

    Poppe, L.J.; Manheim, F. T.; Popenoe, P.

    1992-01-01

    Phosphorite and phosphatic sediments are present in the Georges Bank Basin in marine, Late Cretaceous to Miocene strata equivalent to the Dawson Canyon Formation and Banquereau Formation of offshore Nova Scotia. The Late Cretaceous to Paleocene phosphorite occurs predominantely as sand- and gravel-sized pellets and as cement in conglomeratic aggregates. The Eocene and Miocene phosphate occurs mainly as fine-very fine sand-size spheroidal-avoidal pellets in unconsolidated clayey silts. The older phosphorites form intraformational conglomerates that are the result of a winnowed finer-grained matrix, leaving lag deposits of phosphorite. We present evidence that most of the Eocene and Miocene phosphate is primary and formed during marine trangressions. Our observations extend the geographic and temporal limits of the major phosphogenic system of the Western North Atlantic northward and through time. However, compared to the well-known phosphorite deposits along the southeastern margin of the U.S.A., these northern deposits are not of commercial scale due to a high terrigenous input and the lack of a mechanism capable of driving persistant upwelling. ?? 1992.

  9. Two major Cenozoic episodes of phosphogenesis recorded in equatorial Pacific seamount deposits

    USGS Publications Warehouse

    Hein, J.R.; Hsueh-Wen, Yeh; Gunn, S.H.; Sliter, W.V.; Benninger, L.M.; Chung-Ho, Wang

    1993-01-01

    The phosphorites occur in a wide variety of forms, but most commonly carbonate fluorapatite (CFA) replaced middle Eocene and older carbonate sediment in a deep water environment (>1000 m). Element ratios distinguish seamount phosphorites from continental margin, plateau, and insular phosphorites. Uranium and thorium contents are low and total rare earch element (REE) contents are generally high. The paleoceanographic conditions initiated and sustained development of phosphorite by accumulation of dissolved phosphorus in the deep sea during relatively stable climatic conditions when oceanic circulation was sluggish. Fluctuations in climate, sealevel, and upwelling that accompanied the climate transitions may have driven cycles of enrichment and depletion of the deep-sea phosphorus reservoir. -from Authors

  10. [Optimization of vermicomposting of organics enriched with phosphorites with participation of phosphate-mobilizing microorganisms].

    PubMed

    Hatsenko, M V; Volkohon, V V

    2010-01-01

    Active strains of microorganisms capable to mobilize phosphorus from poorly soluble compounds were isolated from the vermicompost. Representatives of Pseudomonas genus dominate in assemblages of phosphate-mobilizing humus microbiota. The strains Pseudomonas sp. 17 and Pseudomonas sp. 22, which promote liberation of the greatest quantity of water-soluble phosphorus were selected under vermicomposting of organics enriched with phosphorites with participation of active phosphate-mobilizing microorganisms. The use of compost derived with participation of Pseudomonas sp. 17 in cucumbers growth technologies makes the plants development better and raises the cultures productivity.

  11. Phosphate rock formation and marine phosphorus geochemistry: the deep time perspective.

    PubMed

    Filippelli, Gabriel M

    2011-08-01

    The role that phosphorite formation, the ultimate source rock for fertilizer phosphate reserves, plays in the marine phosphorus (P) cycle has long been debated. A shift has occurred from early models that evoked strikingly different oceanic P cycling during times of widespread phosphorite deposition to current thinking that phosphorite deposits may be lucky survivors of a series of inter-related tectonic, geochemical, sedimentological, and oceanic conditions. This paradigm shift has been facilitated by an awareness of the widespread nature of phosphogenesis-the formation of authigenic P-bearing minerals in marine sediments that contributes to phosphorite formation. This process occurs not just in continental margin sediments, but in deep sea oozes as well, and helps to clarify the driving forces behind phosphorite formation and links to marine P geochemistry. Two processes come into play to make phosphorite deposits: chemical dynamism and physical dynamism. Chemical dynamism involves the diagenetic release and subsequent concentration of P-bearing minerals particularly in horizons, controlled by a number of sedimentological and biogeochemical factors. Physical dynamism involves the reworking and sedimentary capping of P-rich sediments, which can either concentrate the relatively heavy and insoluble disseminated P-bearing minerals or provide an episodic change in sedimentology to concentrate chemically mobilized P. Both processes can result from along-margin current dynamics and/or sea level variations. Interestingly, net P accumulation rates are highest (i.e., the P removal pump is most efficient) when phosphorites are not forming. Both physical and chemical pathways involve processes not dominant in deep sea environments and in fact not often coincide in space and time even on continental margins, contributing to the rarity of high-quality phosphorite deposits and the limitation of phosphate rock reserves. This limitation is becoming critical, as the human demand

  12. Morphology and ultrastructure of epilithic versus cryptic, microbial growth in lower Cambrian phosphorites from the Montagne Noire, France.

    PubMed

    Alvaro, J J; Clausen, S

    2010-03-01

    The lower Cambrian grainy phosphorites of the northern Montagne Noire occur interbedded with grey to black, laminated to massive shales and limestones deposited along the edge of a continental shelf, associated with slope-related facies and unstable substrates. The concentration of phosphate took place by repeated alternations of low sedimentation rates and condensation (hardgrounds), in situ early-diagenetic precipitation of fluorapatite, winnowing and polyphase reworking of previously phosphatized skeletons and hardground-derived clasts. The succession of repeated cycles of sedimentation, phosphate concentration, and reworking led to multi-event phosphate deposits rich in allochthonous particles. Phosphogenesis was primarily mediated by microbial activity, which is evidenced by the abundance of phosphatized putative microbial remains. These occur as smooth and segmented filaments, sheaths, and ovoid-shaped coccoids. These simple morphologies commonly form composite frameworks as a result of their aggregation and entanglement, leading to the record of biofilms, microbial mats, and complex networks. These infested the calcitic skeletonized microfossils that littered the substrate. Microbial activity evidences epilithic (anisotropic coatings on skeletons), euendolithic (perforating skeletal walls), and cryptoendolithic (lining inter- and intraparticulate pores) strategies, the latter dominated by bundles of filaments and globular clusters that grew along the cavities of helcionellids and hyoliths. According to their epilithic versus cryptic strategies, microbial populations that penetrated and dwelled inside hard skeletal substrates show different network and colonial morphologies. These early Cambrian shell concentrations were the loci of a stepwise colonization made by saprophytic to mutualistic, cyanobacterial-fungal consortia. Their euendolithic and cryptoendolithic ecological niches provided microbial refugia to manage the grazing impact mainly led by metazoans.

  13. Microbial pathways and palaeoenvironmental conditions involved in the formation of phosphorite grains, Safaga District, Egypt

    NASA Astrophysics Data System (ADS)

    Salama, Walid; El-Kammar, Ahmed; Saunders, Martin; Morsy, Rania; Kong, Charlie

    2015-07-01

    Phosphatic grains of the shallow marine phosphorite deposits of Egypt are classified as either phosphatic bioclasts preserving biological structure (e.g. skeletal fragments such as fish bones and teeth) or phosphatic peloids and intraclasts. This study describes the destructive and constructive microbial pathways represented by bioerosion of bones by endolithic cyanobacteria and accretion of phosphatic peloids by bacteria. The palaeoenvironmental conditions and post-depositional/diagenetic history of these grains have also been considered. Scanning and transmission electron microscopy showed that the phosphatic peloids under transmitted light microscopy are composed mainly of microspheres (0.5 to 2.5 μm) similar in shape and size to coccoid-like bacteria. Chemical mapping showed that these microspheres are composed of carbonate-fluorapatite (CFA) and surrounded by degraded carbonaceous matrix. These grains are suggested to be reworked from pre-existing microbial mats during transgressive-regressive cycles affecting the southern Tethyan Campanian-Maastrichtian shallow continental shelf. The bioerosion of phosphatic bones is characterized by a network of meandering microborings that penetrated inward from the bone surface by endolithic cyanobacteria. The bioerosion of bones resulted in a gradual centripetal digestion and conversion of bones into micritic phosphate peloids. The bioerosion mechanism is probably started in the acidic sheath surrounding cyanobacteria followed by supersaturation of PO4 and reprecipitation of crystalline CFA as electron dense remineralized rims. Electron microprobe microanalyses showed that the remineralized microbored areas are higher in CaO, P2O5, and F and depleted in Cl, relative to unaltered bones. A gradual demineralization of remineralized rims followed by dissolution of cyanobacterial cells is probably occurred during diagenesis and meteoric water alteration leaving behind empty microborings. Bone exposed to meteoric water

  14. A mid-Permian chert event: widespread deposition of biogenic siliceous sediments in coastal, island arc and oceanic basins

    USGS Publications Warehouse

    Murchey, B.L.; Jones, D.L.

    1992-01-01

    Radiolarian and conodont of Permian siliceous rocks from twenty-three areas in teh the circum-Pacific and Mediterranean regions reveal a widespread Permian Chert Event during the middle Leonardian to Wordian. Radiolarian- and (or) sponge spicule-rich siliceous sediments accumulated beneath high productivity zones in coastal, island arc and oceanic basins. Most of these deposits now crop out in fault-bounded accreted terranes. Biogenic siliceous sediments did not accumulate in terranes lying beneath infertile waters including the marine sequences in terranes of northern and central Alaska. The Permian Chert Event is coeval with major phosphorite deposition along the western margin of Pangea (Phosphoria Formation and related deposits). A well-known analogue for this event is middle Miocene deposition of biogenic siliceous sediments beneath high productivity zones in many parts of the Pacific and concurrent deposition of phosphatic as well as siliceous sediments in basins along the coast of California. Interrelated factors associated with both the Miocene and Permian depositional events include plate reorientations, small sea-level rises and cool polar waters. ?? 1992.

  15. Restoration of Soils and Vegetation on Reclamation Sites of the Kingisepp Phosphorite Field

    NASA Astrophysics Data System (ADS)

    Dmitrakova, Ya. A.; Abakumov, E. V.

    2018-05-01

    Processes of initial soil formation were studied on long-term monitoring plots on dump rocks of quarry no. 3 of the Phosphorite production company in Kingisepp district of Leningrad oblast. Observations were performed in 1998, 2004, and 2014. It was shown that vegetation succession on the plots proceeds relatively quickly, and that the species composition of phytocenoses formed is typical of the areas with soddy-calcareous soils. Soil development proved to be correlated with the development of vegetation. Maximum changes in soil characteristics were observed with an increase in the density of forest vegetation and a decrease in the role of herbs. The molecular composition of humic acids in the studied soils remained stable; in particular, the ratio of aliphatic to alkyl aromatic fragments was virtually constant. This phenomenon could be due to the great amount of aliphatic components in the falloff of coniferous species subjected to humification.

  16. The geology of the Florida land-pebble phosphate deposits

    USGS Publications Warehouse

    Cathcart, J.B.; Blade, L.V.; Davidson, D.F.; Ketner, K.B.

    1952-01-01

    The land-pebble phosphate district is on the Gulf Coastal Plain of Florida. The phosphate deposits are in the Bone Valley formation, dated Pliocene by most writers. These strata overlie the Miocene Hawthorn formation and are overlain by consolidated sands 3 to 20 feet thick. The minable phosphate deposits, called “matrix” in the district, range from a featheredge to about 50 feet in thickness and consist of phosphatic pellets and nodules, quartz sand, and montmorillonitic clay in about equal proportions. Locally the matrix displays cross-bedding and horizontal laminations, but elsewhere it is structureless. The phosphorite particles, composed largely of carbonate-fluorapatite, range in diameter from less than 0.1 mm to about 60 cm and in P2O5 content from 30 to 36 percent. Coarse-pebble deposits, containing 30 to 34 percent P2O5 are found mainly on basement highs; and fine-pebble deposits, containing 32 to 36 percent P2O5 are, are found in basement lows. Deposits in the northern part of the field contain more phosphate particles and their P2O5 content is higher than those in the southern part. The upper part of the phosphatic strata is leached to an advanced degree and consists of quartz sand and clay-sized particules of pseudowavellite and wavellite. The leached zone ranges in thickness from a featheredge to 60 feet. The origin of the land-pebble deposits is incompletely known. Possible modes of origin are a residuum of Miocene age, or a reworked residuum of Pliocene or Quaternary age.

  17. Ferromanganese deposits from the Gulf of Alaska seamount province: mineralogy, chemistry, and origin.

    USGS Publications Warehouse

    Koski, R.A.

    1988-01-01

    Petrographic and chemical data presented and discussed permit the following conclusions regarding the high-latitude Gulf of Alaska (GA) Fe-Mn deposits: 1) thick (10-50 mm) Fe-Mn crusts form on alkali-basalt and volcaniclastic substrates by hydrogenetic processes, contain delta -MnO2 as the principal Mn phase, and have compositions similar to those of seamount crusts from comparable depths in the Hawaiian archipelago. GA crusts have higher Mn/Fe and lower Co contents than crusts from low-altitude, central Pacific seamounts; 2) thin (<10 mm) crusts on tuffaceous conglomerate, sandstone and phosphorite have a high proportion of crystalline Mn oxides and are genetically related to vein deposits; 3) vein deposits of todorokite and cryptomelane form during low-T oxidative diagenesis of volcanogenic sediment. Mn and other transition metals are supplied during the initial palagonitization of basaltic glass. The oxidation of Fe2+ to Fe3+ in palagonite and the dissolution of the diluted microfossil fraction of the sediment lower the Eh of the ambient pore fluid and enhance the solubility of Mn2+. The K released during the formation of palagonite may be redeposited in secondary phyllosilicate minerals, phillipsite, todorokite and cryptomelane; 4) the vein deposits formed soon after the deposition of sediment derived from the erosion and mass wasting of Mill Seamount but before crust deposition. Therefore, the deposition of hydrogenous crusts and the deposition of diagenetic veins are chemically distinct processes in time and space.-J.M.H.

  18. Mineral resources of the Atlantic Exclusive Economic Zone

    USGS Publications Warehouse

    Dillon, William P.

    1984-01-01

    Potential mineral resources of the Atlantic Exclusive Economic Zone (including the Gulf of Mexico and US Caribbean areas) include petroleum, sand and gravel, phosphorite, placer deposits of heavy mineral sands, ferromanganese nodules, and fresh water. Although major efforts have been made to search for petroleum, the oil and gas resources of the region are well known only in the western Gulf Shelf and more exploration is under way. Heavy-mineral placer deposits, which may be sources of titanium, gold, rare earths, etc. , have been sampled, but the extent and, therefore, economic value of the deposits have not been identified. Sand and gravel, phosphorite, and ferromanganese nodules all are represented by fairly well established deposits, and only modified market conditions would be necessary to cause detailed exploration and mining.

  19. The stable isotopic composition of a phosphorite deposit: δ13C, δ34S, and δ18O

    USGS Publications Warehouse

    Piper, D.Z.; Kolodny, Y.

    1987-01-01

    The stable isotopes of carbon and sulfur in a major marine sedimentary phosphate deposit from the northwestern United States (the Phosphoria Formation of Permian age) characterize the chemical properties of the depositional environment. The δ34S and δ13C analyses suggest deposition under conditions of variable redox from a solution the acidity of which was controlled by reaction with carbonate rocks and exchange with seawater. The δ18O concentration of apetite indicates phosphatization in a shallow sea, during three glacial and intervening interglacial stages. These data tend to corroborate the interpretation of field studies by others, that the apatite formed on a continental shelf in an area of intense oceanic upwelling during several episodes of sea level change. 

  20. Petrographic Descriptions of Selected Rock Specimens From the Meade Peak Phosphatic Shale Member, Phosphoria Formation (Permian), Southeastern Idaho

    USGS Publications Warehouse

    Johnson, Edward A.; Grauch, Richard I.; Herring, James R.

    2007-01-01

    structures are absent except in some muddy dolomitized calclithites. Organic claystones, muddy siltstones, and dolomitized calclithites are detrital deposits. Many rocks in the Meade Peak contain calcite and apatite as fracture fillings and vug linings. As expected, peloidal phosphorites are most common in ore zones, and detrital rocks are most common in waste zones. Mine-specific marker beds are mostly composed of dolomitized calclithite.

  1. The controversial "Cambrian" fossils of the Vindhyan are real but more than a billion years older.

    PubMed

    Bengtson, Stefan; Belivanova, Veneta; Rasmussen, Birger; Whitehouse, Martin

    2009-05-12

    The age of the Vindhyan sedimentary basin in central India is controversial, because geochronology indicating early Proterozoic ages clashes with reports of Cambrian fossils. We present here an integrated paleontologic-geochronologic investigation to resolve this conundrum. New sampling of Lower Vindhyan phosphoritic stromatolitic dolomites from the northern flank of the Vindhyans confirms the presence of fossils most closely resembling those found elsewhere in Cambrian deposits: annulated tubes, embryo-like globules with polygonal surface pattern, and filamentous and coccoidal microbial fabrics similar to Girvanella and Renalcis. None of the fossils, however, can be ascribed to uniquely Cambrian or Ediacaran taxa. Indeed, the embryo-like globules are not interpreted as fossils at all but as former gas bubbles trapped in mucus-rich cyanobacterial mats. Direct dating of the same fossiliferous phosphorite yielded a Pb-Pb isochron of 1,650 +/- 89 (2sigma) million years ago, confirming the Paleoproterozoic age of the fossils. New U-Pb geochronology of zircons from tuffaceous mudrocks in the Lower Vindhyan Porcellanite Formation on the southern flank of the Vindhyans give comparable ages. The Vindhyan phosphorites provide a window of 3-dimensionally preserved Paleoproterozoic fossils resembling filamentous and coccoidal cyanobacteria and filamentous eukaryotic algae, as well as problematic forms. Like Neoproterozoic phosphorites a billion years later, the Vindhyan deposits offer important new insights into the nature and diversity of life, and in particular, the early evolution of multicellular eukaryotes.

  2. Paleontologic and stratigraphic relations of phosphate beds in Upper Cretaceous rocks of the Cordillera Oriental, Colombia

    USGS Publications Warehouse

    Maughan, Edwin K.; Zambrano O., Francisco; Mojica G., Pedro; Abozaglo M., Jacob; Pachon P., Fernando; Duran R., Raul

    1979-01-01

    Phosphorite crops out in the Cordillera Oriental of the Colombian Andes in rocks of Late Cretaceous age as strata composed mostly of pelletal carbonate fluorapatite. One stratum of Santonian age near the base of the Galembo Member of the La Luna Formation crops out at many places in the Departments of Santander and Norte de Santander and may be of commercial grade. This stratum is more than one meter thick at several places near Lebrija and near Sardinata, farther south it is locally one meter thick or more near the base of the Guadalupe Formation in the Department of Boyaca. Other phosphorite beds are found at higher stratigraphic levels in the Galembo Member and the Guadalupe Formation, and at some places these may be commercial also. A stratigraphically lower phosphorite occurs below the Galembo Member in the Capacho Formation (Cenomanian age) in at least one area near the town of San Andres, Santander. A phosphorite or pebbly phosphate conglomerate derived from erosion of the Galembo Member forms the base of the Umir Shale and the equivalent Colon Shale at many places. Deposition of the apatite took place upon the continental shelf in marine water of presumed moderate depth between the Andean geosyncline and near-shore detrital deposits adjacent to the Guayana shield. Preliminary calculations indicate phosphorite reserves of approximately 315 million metric tons in 9 areas, determined from measurements of thickness, length of the outcrop, and by projecting the reserves to a maximum of 1,000 meters down the dip of the strata into the subsurface. Two mines were producing phosphate rock in 1969; one near Turmeque, Boyaca, and the other near Tesalia, Huila.

  3. Gondolellid conodonts and depositional setting of the Phosphoria Formation

    USGS Publications Warehouse

    Wardlaw, Bruce R.

    2015-01-01

    The Phosphoria Formation and related rocks were deposited over an 8.9 m.y. interval beginning approximately 274.0Ma and ending approximately 265.1Ma. The Meade Peak Phosphatic Shale Member was deposited in southeastern Idaho and adjacent Wyoming over 5.4 m.y. from approximately 273.2 to 268.6 Ma. The Retort Phosphatic Shale Member was deposited in southwestern Montana and west-central Wyoming over 1.3 m.y. from approximately 267.4 to 266.1Ma. The base of the Roadian Stage of the Middle Permian occurs within the lower phosphate zone of the Meade Peak. The base of the Wordian Stage occurs within the upper phosphate zone of the Meade Peak. The presence of a cool-water brachiopod fauna, cool-water conodont faunas, and the absence of fusulinids throughout the Phosphoria basin indicate the presence of pervasive cool, upwelling waters. Acritarchs are intimately associated with phosphorites and phosphatic shales and may have been the primary organic producer to help drive phosphate production. The gondolellid conodont fauna of the Phosphoria Formation links a geographic cline of Jinogondolella nankingensis from the Delaware basin, West Texas, to the Sverdrup basin, Canadian Arctic, and shows distinct differentiation in species distribution, as do other conodont groups, within the Phosphoria basin. Ten species and two subspecies of gondolellid conodonts are recognized from the Phosphoria Formation and related rocks that belong to Mesogondolella and Jinogondolella.

  4. Geographical coincidence of high heat flow, high seismicity, and upwelling, with hydrocarbon deposits, phosphorites, evaporites, and uranium ores.

    PubMed

    Libby, L M; Libby, W F

    1974-10-01

    Oil deposits occur in deep sediments, and appear to be organic matter that has been transformed through the action of geothermal heat and pressure. Deep sediments, rich in biological remains, are created by ocean upwelling, caused in part by high geothermal heat flow through the sea bottom. Such regions correlate with enhanced seismic activity. We look for correlations of seismicity, high heat flux, petroleum, uranium, phosphates, and salts, deposited from abundant plant life. These may be useful in discovering more petroleum and coal. We estimate that the known world reserves of petroleum and coal are about 10(-4) of the total of buried biogenic carbon.

  5. Geographical Coincidence of High Heat Flow, High Seismicity, and Upwelling, with Hydrocarbon Deposits, Phosphorites, Evaporites, and Uranium Ores

    PubMed Central

    Libby, L. M.; Libby, W. F.

    1974-01-01

    Oil deposits occur in deep sediments, and appear to be organic matter that has been transformed through the action of geothermal heat and pressure. Deep sediments, rich in biological remains, are created by ocean upwelling, caused in part by high geothermal heat flow through the sea bottom. Such regions correlate with enhanced seismic activity. We look for correlations of seismicity, high heat flux, petroleum, uranium, phosphates, and salts, deposited from abundant plant life. These may be useful in discovering more petroleum and coal. We estimate that the known world reserves of petroleum and coal are about 10-4 of the total of buried biogenic carbon. Images PMID:16592185

  6. The controversial “Cambrian” fossils of the Vindhyan are real but more than a billion years older

    PubMed Central

    Bengtson, Stefan; Belivanova, Veneta; Rasmussen, Birger; Whitehouse, Martin

    2009-01-01

    The age of the Vindhyan sedimentary basin in central India is controversial, because geochronology indicating early Proterozoic ages clashes with reports of Cambrian fossils. We present here an integrated paleontologic–geochronologic investigation to resolve this conundrum. New sampling of Lower Vindhyan phosphoritic stromatolitic dolomites from the northern flank of the Vindhyans confirms the presence of fossils most closely resembling those found elsewhere in Cambrian deposits: annulated tubes, embryo-like globules with polygonal surface pattern, and filamentous and coccoidal microbial fabrics similar to Girvanella and Renalcis. None of the fossils, however, can be ascribed to uniquely Cambrian or Ediacaran taxa. Indeed, the embryo-like globules are not interpreted as fossils at all but as former gas bubbles trapped in mucus-rich cyanobacterial mats. Direct dating of the same fossiliferous phosphorite yielded a Pb–Pb isochron of 1,650 ± 89 (2σ) million years ago, confirming the Paleoproterozoic age of the fossils. New U–Pb geochronology of zircons from tuffaceous mudrocks in the Lower Vindhyan Porcellanite Formation on the southern flank of the Vindhyans give comparable ages. The Vindhyan phosphorites provide a window of 3-dimensionally preserved Paleoproterozoic fossils resembling filamentous and coccoidal cyanobacteria and filamentous eukaryotic algae, as well as problematic forms. Like Neoproterozoic phosphorites a billion years later, the Vindhyan deposits offer important new insights into the nature and diversity of life, and in particular, the early evolution of multicellular eukaryotes. PMID:19416859

  7. A review of phosphate mineral nucleation in biology and geobiology.

    PubMed

    Omelon, Sidney; Ariganello, Marianne; Bonucci, Ermanno; Grynpas, Marc; Nanci, Antonio

    2013-10-01

    Relationships between geological phosphorite deposition and biological apatite nucleation have often been overlooked. However, similarities in biological apatite and phosphorite mineralogy suggest that their chemical formation mechanisms may be similar. This review serves to draw parallels between two newly described phosphorite mineralization processes, and proposes a similar novel mechanism for biologically controlled apatite mineral nucleation. This mechanism integrates polyphosphate biochemistry with crystal nucleation theory. Recently, the roles of polyphosphates in the nucleation of marine phosphorites were discovered. Marine bacteria and diatoms have been shown to store and concentrate inorganic phosphate (Pi) as amorphous, polyphosphate granules. Subsequent release of these P reserves into the local marine environment as Pi results in biologically induced phosphorite nucleation. Pi storage and release through an intracellular polyphosphate intermediate may also occur in mineralizing oral bacteria. Polyphosphates may be associated with biologically controlled apatite nucleation within vertebrates and invertebrates. Historically, biological apatite nucleation has been attributed to either a biochemical increase in local Pi concentration or matrix-mediated apatite nucleation control. This review proposes a mechanism that integrates both theories. Intracellular and extracellular amorphous granules, rich in both calcium and phosphorus, have been observed in apatite-biomineralizing vertebrates, protists, and atremate brachiopods. These granules may represent stores of calcium-polyphosphate. Not unlike phosphorite nucleation by bacteria and diatoms, polyphosphate depolymerization to Pi would be controlled by phosphatase activity. Enzymatic polyphosphate depolymerization would increase apatite saturation to the level required for mineral nucleation, while matrix proteins would simultaneously control the progression of new biological apatite formation.

  8. High phosphate availability as a possible cause for massive cyanobacterial production of oxygen in the Paleoproterozoic atmosphere

    NASA Astrophysics Data System (ADS)

    Papineau, Dominic; Purohit, Ritesh; Fogel, Marilyn L.; Shields-Zhou, Graham A.

    2013-01-01

    The deposition of major Precambrian phosphorites was restricted to times of global change and atmospheric oxygenation at both ends of the Proterozoic. Phosphorites formed after highly positive carbon isotope excursions in carbonates deposited during the Paleoproterozoic Lomagundi-Jatuli event and the Neoproterozoic Cryogenian and Ediacaran periods. The correlative step-wise rise in atmospheric oxygen over the Proterozoic has been linked to changes in the carbon cycle. However, the postulated relations between carbon isotope events, phosphorites, and atmospheric oxygenation remain unexplained. Paleoproterozoic carbonates of the Aravalli Supergroup, India, preserve evidence for cyanobacterial blooms in the form of tightly packed stromatolitic columns in the world's oldest significant sedimentary phosphate deposit. Restricted basins of the Lower Aravalli Group with stromatolitic phosphorites in Jhamarkotra, Udaipur, Jhabua, and Sallopat exhibit near-zero δ13Ccarb values and large ranges of δ13Corg values between -33.3‰ and -10.1‰, indicative of a complex carbon cycle. Because phosphate accumulates primarily in oxic sediments, these eutrophic microbial ecosystems likely developed within the photic zone of the shallow, oxygenated marine realm. This is consistent with deposition during the time of increasingly more oxidizing conditions, after the Great Oxidation Event (GOE). Approximately contemporaneous basins without phosphate deposits from Ghasiar, Karouli, Negadia, Umra, and Babarmal exhibit a range of positive δ13Ccarb excursions, some with values up to +11.2‰, that suggest high rates of organic carbon burial, and others with moderately high δ13Ccarb values around +6‰ or +3‰, that suggest smaller carbon cycle perturbations. The δ15N values of all these rocks vary between -0.7‰ and +3.4‰, and are consistent with the predominance of nitrogen fixation during cyanobacterial blooms in all basin types. Such low nitrogen isotope values are interpreted to

  9. Geochemistry of host rocks in the Howards Pass district, Yukon-Northwest Territories, Canada: implications for sedimentary environments of Zn-Pb and phosphate mineralization

    USGS Publications Warehouse

    Slack, John F.; Falck, Hendrik; Kelley, Karen D.; Xue, Gabriel G.

    2017-01-01

    Detailed lithogeochemical data are reported here on early Paleozoic sedimentary rocks that host the large Howards Pass stratiform Zn-Pb deposits in Yukon-Northwest Territories. Redox-sensitive trace elements (Mo, Re, V, U) and Ce anomalies in members of the Duo Lake Formation record significant environmental changes. During the deposition of lower footwall units (Pyritic siliceous and Calcareous mudstone members), bottom waters were anoxic and sulphidic, respectively; these members formed in a marginal basin that may have become increasingly restricted with time. Relative to lower members, a major environmental change is proposed for deposition of the overlying Lower cherty mudstone member, which contains phosphorite beds up to ∼0.8 m thick in the upper part, near the base of the Zn-Pb deposits. The presence of these beds, together with models for modern phosphorite formation, suggests P input from an upwelling system and phosphorite deposition in an upper slope or outer shelf setting. The overlying Active mudstone member contains stratabound to stratiform Zn-Pb deposits within black mudstone and gray calcareous mudstone. Data for unmineralized black mudstone in this member indicate deposition under diverse redox conditions from suboxic to sulphidic. Especially distinctive in this member are uniformly low ratios of light to heavy rare earth elements that are unique within the Duo Lake Formation, attributed here to the dissolution of sedimentary apatite by downward-percolating acidic metalliferous brines. Strata that overlie the Active member (Upper siliceous mudstone member) consist mainly of black mudstone with thin (0.5–1.5 cm) laminae of fine-grained apatite, recording continued deposition on an upper slope or outer shelf under predominantly suboxic bottom waters. Results of this study suggest that exploration for similar stratiform sediment-hosted Zn-Pb deposits should include the outer parts of ancient continental margins, especially at and near

  10. Sulphur bacteria mediated formation of Palaeoproterozoic phosphorites

    NASA Astrophysics Data System (ADS)

    Joosu, Lauri; Lepland, Aivo; Kirsimäe, Kalle

    2014-05-01

    Modern phosphorite formation is typically associated with high productivity in upwelling areas where apatite (Ca-phosphate) precipitation is mediated by sulphur oxidising bacteria [1]. They inhabit the oxic/anoxic interface within the upper few centimetres of sediment column, accumulating phosphate in their cells under oxic conditions and releasing it rapidly when conditions become anoxic. Sulphur bacteria are known to live in close association with a consortium of anaerobic methane oxidising archaea and syntrophic sulphate-reducing bacteria. Paleoproterozoic, c. 2.0 Ga Zaonega Formation in Karelia, Russia contains several P-rich intervals in the upper part of 1500 m thick succession of organic-rich sedimentary rocks interlayered with mafic tuffs and lavas. Apatite in these P-rich intervals forms impure laminae, lenses and round-oval nodules which diameters typically range from 300 to 1000 μm. Individual apatite particles in P-rich laminae and nodules commonly occur as cylinders that are 1-8 μm long and have diameters of 0.5-4 μm. Cross-sections of best preserved cylindrical apatite particles reveal a thin outer rim whereas the internal parts consist of small anhedral elongated crystallites, intergrown with carbonaceous material. During recrystallization the outer rim thickens towards interior and cylinders may attain hexagonal crystal habit, but their size and shape remains largely unchanged [2]. The sizes of Zaonega nodules are similar to giant sulphide-oxidising bacteria known from modern and ancient settings [3, 4]. Individual apatite cylinders and aggregates have shapes and sizes similar to the methanotrophic archaea that inhabit microbial mats in modern seep/vent areas where they operate in close associations with sulphur-oxidising microbial communities [5]. Seep/vent influence during the Zaonega phosphogenesis is indicated by variable, though positive Eu anomaly, expected in magmatically active sedimentary environment experiencing several lava flows

  11. Summary of reconnaissance for radioactive deposits in Alaska, 1945-1954, and an appraisal of Alaskan uranium possibilities

    USGS Publications Warehouse

    Wedow, Helmuth

    1956-01-01

    carnotite-type deposits. The chief of these areas is the Alaska Peninsula-Cook Inlet area which encompasses most of the reported occurrences of the prospectors' carnotite-type samples. Alaska is also potentially favorable for the occurrence of large bodies of the very low-grade uraniferous sedimentary rocks, such as phosphorites and black shales. This type of deposit, however, has not received much study because of the emphasis on the search for bonanza-type high-grade ores. Uraniferous phosphorites similar to those of Idaho, Montana, and Wyoming occur in northern Alaska on the north flank of the Brooks Range; black shales comparable to the uraniferous shales of the Chattanooga formation of southeastern United States have been noted along the Yukon River near the international boundary. Placer deposits in Alaska have some small potential for the production of the radioactive elements as byproducts of gold- and tin-placer mining. the placer area believed to have the relatively greatest potential in Alaska lies in the Kahiltna River valley where concentrates are known to contain such commercial minerals as ilmenite, cassiterite, platinum, and gold in addition to uranothorianite and monazite. The possibilities of the natural fluids--water and petroleum--have not yet been tested in Alaska to any great extent. Studies of fluids are in progress to determine whether they may be used to discover and define areas potentially favorable for the occurrence of uraniferous lodes.

  12. Geological setting of oil shales in the Permian phosphoria formation and some of the geochemistry of these rocks

    USGS Publications Warehouse

    Maughan, E.K.

    1983-01-01

    Recent studies of the Meade Peak and the Retort Phosphatic Shale Members of the Phosphoria Formation have investigated the organic carbon content and some aspects of hydrocarbon generation from these rocks. Phosphorite has been mined from the Retort and Meade Peak members in southeastern Idaho, northern Utah, western Wyoming and southwestern Montana. Organic carbon-rich mudstone beds associated with the phosphorite in these two members also were natural sources of petroleum. These mudstone beds were differentially buried throughout the region so that heating of these rocks has been different from place to place. Most of the Phosphoria source beds have been deeply buried and naturally heated to catagenetically form hydrocarbons. Deepest burial was in eastern Idaho and throughout most of the northeastern Great Basin where high ambient temperatures have driven the catagenesis to its limit and beyond to degrade or to destroy the hydrocarbons. In southwest Montana, however, burial in some areas has been less than 2 km, ambient temperatures remained low and the kerogen has not produced hydrocarbons (2). In these areas in Montana, the kerogen in the carbonaceous mudstone has retained the potential for hydrocarbon generation and the carbon-rich Retort Member is an oil shale from which hydrocarbons can be synthetically extracted. The Phosphoria Formation was deposited in a foreland basin between the Cordilleran geosyncline and the North American craton. This foreland basin, which coincides with the area of deposition of the two organic carbon-rich mudstone members of the Phosphoria, has been named the Sublett basin (Maughan, 1979). The basin has a northwest-southeast trending axis and seems to have been deepest in central Idaho where deep-water sedimentary rocks equivalent to the Phosphoria Formation are exceptionally thick. The depth of the basin was increasingly shallower away from central Idaho toward the Milk River uplift - a land area in Montana, the ancestral Rocky

  13. The Cretaceous glauconitic sandstones of Abu Tartur, Egypt

    NASA Astrophysics Data System (ADS)

    Pestitschek, Brigitte; Gier, Susanne; Essa, Mahmoud; Kurzweil, Johannes

    2010-05-01

    The Abu Tartur mine is located in the Western Desert of Egypt, 50 km west of El Kharga City. Geologically, the Abu Tartur plateau is built by a sequence of Upper Cretaceous (Campanian - Maastrichtian) phosphorites, black shales and glauconitic sandstones. The phosphate deposits are of great economic importance and have been mined since their discovery in 1967. Outcrop sections were measured, sampled, sedimentologically characterized and described. One specific glaucony layer was investigated mineralogically and chemically in detail and compared to a subsurface sample from the mine. Two depositional regimes can be interpreted based on sedimentary architecture and structures: 1) a deeper-water hemipelagic environment, where phosphorites and organic carbon-rich shales were deposited and 2) a shallower, prograding higher energy shelf environment with glauconies. From a sequence stratigraphic perspective 1) was deposited during the transgressive systems tract and the early highstand while 2) was deposited during the remaining highstand and a lowstand prograding wedge (Glenn & Arthur, 1990). Petrographic and SEM investigations show that the glaucony grains are of authochtonous origin. XRF, EMPA and thin-section analyses show that the glaucony grains from the outcrop differ significantly in their chemical composition, morphology and color from the grains of the mine sample. The fresh glauconies are enriched in Fe2O3 and K2O compared to the surface samples. XRD analyses of the clay fraction of the six outcrop samples and the mine sample show that the grains consist of illite(glauconite)/smectite mixed-layers, with more illite layers (80 %) in the mine sample. The charge distribution diagram muscovite-pyrophyllite-celadonite shows a clear trend from smectitic glaucony to illitic glaucony, the mine sample plots exactly in the field for glauconites. All these features indicate that the surface samples are strongly altered by weathering and that glauconite progressively

  14. Phosphorus as a potential guide in the search for extinct life on Mars.

    PubMed

    Weckwerth, G; Schidlowski, M

    1995-03-01

    In contrast to the search for extant organisms, the quest for fossil remains of life on Mars need not be guided by the presence of water and organic compounds on the present surface. An appropriate tracer might be the element phosphorus which is a common constituent of living systems. Utilizing terrestrial analogues, it should preferentially exist in the form of sedimentary calcium phosphate (phosphorites), which would have readily resisted changing conditions on Mars. Moreover, higher ratios of P/Th in phosphorites in comparison to calcium phosphates from magmatic rocks give us the possibility to distinguish them from inorganically formed phosphorus deposits at or close to the Martian surface. Identification of anomalous phosphorus enrichments by remote sensing or in situ analysis could be promising approaches for selecting areas preferentially composed of rocks with remains of extinct life.

  15. Phosphogenesis in the 2460 and 2728 million-year-old banded iron formations as evidence for biological cycling of phosphate in the early biosphere

    PubMed Central

    Li, Yi-Liang; Sun, Si; Chan, Lung S

    2013-01-01

    The banded iron formation deposited during the first 2 billion years of Earth's history holds the key to understanding the interplay between the geosphere and the early biosphere at large geological timescales. The earliest ore-scale phosphorite depositions formed almost at ∼2.0–2.2 billion years ago bear evidence for the earliest bloom of aerobic life. The cycling of nutrient phosphorus and how it constrained primary productivity in the anaerobic world of Archean–Palaeoproterozoic eons are still open questions. The controversy centers about whether the precipitation of ultrafine ferric oxyhydroxide due to the microbial Fe(II) oxidation in oceans earlier than 1.9 billion years substantially sequestrated phosphate, and whether this process significantly limited the primary productivity of the early biosphere. In this study, we report apatite radial flowers of a few micrometers in the 2728 million-year-old Abitibi banded iron formation and the 2460 million-year-old Kuruman banded iron formation and their similarities to those in the 535 million-year-old Lower Cambrian phosphorite. The lithology of the 535 Million-year-old phosphorite as a biosignature bears abundant biomarkers that reveal the possible similar biogeochemical cycling of phosphorus in the Later Archean and Palaeoproterozoic oceans. These apatite radial flowers represent the primary precipitation of phosphate derived from the phytoplankton blooms in the euphotic zones of Neoarchean and Palaoeproterozoic oceans. The unbiased distributions of the apatite radial flowers within sub-millimeter bands do not support the idea of an Archean Crisis of Phosphate. This is the first report of the microbial mediated mineralization of phosphorus before the Great Oxidation Event when the whole biosphere was still dominated by anaerobic microorganisms. PMID:23404127

  16. Phosphogenesis in the 2460 and 2728 million-year-old banded iron formations as evidence for biological cycling of phosphate in the early biosphere.

    PubMed

    Li, Yi-Liang; Sun, Si; Chan, Lung S

    2012-01-01

    The banded iron formation deposited during the first 2 billion years of Earth's history holds the key to understanding the interplay between the geosphere and the early biosphere at large geological timescales. The earliest ore-scale phosphorite depositions formed almost at ∼2.0-2.2 billion years ago bear evidence for the earliest bloom of aerobic life. The cycling of nutrient phosphorus and how it constrained primary productivity in the anaerobic world of Archean-Palaeoproterozoic eons are still open questions. The controversy centers about whether the precipitation of ultrafine ferric oxyhydroxide due to the microbial Fe(II) oxidation in oceans earlier than 1.9 billion years substantially sequestrated phosphate, and whether this process significantly limited the primary productivity of the early biosphere. In this study, we report apatite radial flowers of a few micrometers in the 2728 million-year-old Abitibi banded iron formation and the 2460 million-year-old Kuruman banded iron formation and their similarities to those in the 535 million-year-old Lower Cambrian phosphorite. The lithology of the 535 Million-year-old phosphorite as a biosignature bears abundant biomarkers that reveal the possible similar biogeochemical cycling of phosphorus in the Later Archean and Palaeoproterozoic oceans. These apatite radial flowers represent the primary precipitation of phosphate derived from the phytoplankton blooms in the euphotic zones of Neoarchean and Palaoeproterozoic oceans. The unbiased distributions of the apatite radial flowers within sub-millimeter bands do not support the idea of an Archean Crisis of Phosphate. This is the first report of the microbial mediated mineralization of phosphorus before the Great Oxidation Event when the whole biosphere was still dominated by anaerobic microorganisms.

  17. NONFUEL MINERAL RESOURCES OF THE PACIFIC EXCLUSIVE ECONOMIC ZONE.

    USGS Publications Warehouse

    Clague, David; Bischoff, James; Howell, David

    1984-01-01

    The Pacific Exclusive Economic Zone contains a variety of hard mineral resources. Sand and gravel and their associated placer deposits of heavy minerals are the most likely to be developed in the near future, but offshore and deep water deposits of phosphorite, abyssal manganese nodules, ferromanganese crusts enriched in cobalt, and massive sulfide deposits all represent future resources. The distribution, extent, and formation of these deposits are poorly understood and will be clarified only with additional exploration, framework geologic mapping, and study of the processes by which these resources form. It is pointed out that the initial discovery of most hard-mineral resources in the EEZ was made during routine scientific marine-geologic surveys aimed at understanding the framework geology and geologic processes of an offshore region.

  18. Sedimentary phosphate and associated fossil bacteria in a Paleoproterozoic tidal flat in the 1.85 Ga Michigamme Formation, Michigan, USA

    NASA Astrophysics Data System (ADS)

    Hiatt, Eric E.; Pufahl, Peir K.; Edwards, Cole T.

    2015-04-01

    Phosphorus is a nutrient fundamental to life and when it precipitates in modern environments bacteria are intimately involved in its release, concentration, and mineralization. Preserved fossil bacteria in phosphate crusts and grains from the ca. 1850 million-year-old Bijiki Iron Formation Member of the Michigamme Formation, Michigan provide insight into the longevity and nature of this relationship. The Michigamme Formation accumulated near the end of the Earth's initial phosphogenic episode (ca. 2.2 and 1.8 Ga) to produce one of the first granular phosphorites. Phosphatic lithofacies consist of fine- to medium-sand-sized francolite peloids concentrated on bedding surfaces in peritidal facies. Granular beds are up to 2 cm thick and peloids are often partially to completely replaced by dolomite and chert. The grains contain organic matter and pyrite framboids that suggest bacterial breakdown of organic matter and bacterial sulfate reduction. The peritidal nature of phosphorite in the Michigamme Formation is in sharp contrast to Phanerozoic phosphogenic environments in deeper coastal upwelling settings. Peritidal settings were well suited for phosphogenesis under the very low oxygen and low dissolved sulfate levels of the Paleoproterozoic as cyanobacteria produced oxygen in shallow water and evaporation led to increased sulfate concentrations. Such concomitant processes helped establish focused redox interfaces in the sediment that chemosynthetic bacterial communities (sulfur oxidizers, reducers, forms that concentrate P, and possibly iron oxidizers) could exploit. Phosphate released from organic matter by heterotrophic bacteria and Fe-redox pumping was further concentrated by these chemotrophs; a process that forms late Neoproterozoic to Phanerozoic phosphorites but on a much larger scale. This early example of a granular phosphorite demonstrates that, like their Phanerozoic counterparts, Paleoproterozoic phosphorites are the concentrated indirectly biomineralized

  19. Hierarchy of sedimentary discontinuity surfaces and condensed beds from the middle Paleozoic of eastern North America: Implications for cratonic sequence stratigraphy

    USGS Publications Warehouse

    McLaughlin, P.I.; Brett, Carlton E.; Wilson, M.A.

    2008-01-01

    Sedimentological analyses of middle Paleozoic epeiric sea successions in North America suggest a hierarchy of discontinuity surfaces and condensed beds of increasing complexity. Simple firmgrounds and hardgrounds, which are comparatively ephemeral features, form the base of the hierarchy. Composite hardgrounds, reworked concretions, authigenic mineral crusts and monomictic intraformational conglomerates indicate more complex histories. Polymictic intraformational conglomerates, ironstones and phosphorites form the most complex discontinuity surfaces and condensed beds. Complexity of discontinuities is closely linked to depositional environments duration of sediment starvation and degree of reworking which in turn show a relationship to stratigraphic cyclicity. A model of cratonic sequence stratigraphy is generated by combining data on the complexity and lateral distribution of discontinuities in the context of facies successions. Lowstand, early transgressive and late transgressive systems tracts are representative of sea-level rise. Early and late transgressive systems tracts are separated by the maximum starvation surface (typically a polymictic intraformational conglomerate or condensed phosphorite), deposited during the peak rate of sea-level rise. Conversely the maximum flooding surface, representing the highest stand of sea level, is marked by little to no break in sedimentation. The highstand and falling stage systems tracts are deposited during relative sea-level fall. They are separated by the forced-regression surface, a thin discontinuity surface or condensed bed developed during the most rapid rate of sea-level fall. The lowest stand of sea level is marked by the sequence boundary. In subaerially exposed areas it is occasionally modified as a rockground or composite hardground.

  20. New Insights into an Old Cycle: The Marine Phosphorus Cycle and the Formation of Critical Phosphate Rock Resources (Invited)

    NASA Astrophysics Data System (ADS)

    Filippelli, G. M.

    2010-12-01

    -identified minable reservoirs of ore-grade P are found in the United States, in China, and in Morocco. Numerous less-economic sedimentary deposits exist, but these deposits are more dilute and represent former marine settings without the trifecta of productivity, geochemistry and sedimentology that makes phosphorites economically viable.

  1. Determination of the oxidation state of uranium in apatite and phosphorite deposits

    USGS Publications Warehouse

    Clarke, R.S.; Altschuler, Z.S.

    1958-01-01

    Geological and mineralogical evidence indicate that the uranium present in apatite may proxy for calcium in the mineral structure as U(IV). An experimental investigation was conducted and chemical evidence was obtained that establishes the presence of U(IV) in apatite. The following analytical procedure was developed for the determination of U(IV). Carbonatefluorapatite is dissolved in 1.5 M orthophosphoric acid at a temperature of 5??C or slightly below and fluorapatite is dissolved in cold 1.2 M hydrochloric acid (approximately 5??C) containing 1.5 g of hydroxylamine hydrochloride per 100 ml. Uranium(IV) is precipitated by cupferron using titanium as a carrier. The uranium in the precipitate is separated by use of the ethyl acetate extraction procedure and determined fluorimetrically. The validity and the limitations of the method have been established by spike experiments. ?? 1958.

  2. Manganese and ferromanganese ores from different tectonic settings in the NW Himalayas, Pakistan

    NASA Astrophysics Data System (ADS)

    Tahir Shah, Mohammad; Moon, Charles J.

    2007-02-01

    In Pakistan manganese and ferromanganese ores have been reported from the Hazara area of North West Frontier Province, Waziristan agencies in the Federally Administered Tribal Areas and the Lasbela-Khuzdar regions of Baluchistan. This study is focused on comparison of mineralogy and geochemistry of the continental ferromanganese ores of Hazara and the ophiolitic manganese ores of the Waziristan area of Pakistan. In the Hazara area, ferromanganese ores occur at Kakul, Galdanian and Chura Gali, near Abbottabad, within the Hazira Formation of the Kalachitta-Margala thrust belt of the NW Himalayas of the Indo-Pakistan Plate. The Cambrian Hazira Formation is composed of reddish-brown ferruginous siltstone, with variable amounts of clay, shale, ferromanganese ores, phosphorite and barite. In Waziristan, manganese ores occur at Shuidar, Mohammad Khel and Saidgi, within the Waziristan ophiolite complex, on the western margin of the Indo-Pakistan Plate in NW Pakistan. These banded and massive ores are hosted by metachert and overlie metavolcanics. The ferromanganese ores of the Hazara area contain variable amount of bixbyite, partridgeite, hollandite, pyrolusite and braunite. Bixbyite and partridgeite are the dominant Mn-bearing phases. Hematite dominates in Fe-rich ores. Gangue minerals are iron-rich clay, alumino-phosphate minerals, apatite, barite and glauconite are present in variable amounts, in both Fe-rich and Mn-rich varieties. The texture of the ore phases indicates greenschist facies metamorphism. The Waziristan ores are composed of braunite, with minor pyrolusite and hollandite. Hematite occurs as an additional minor phase in the Fe-rich ores of the Shuidar area. The only silicate phase in these ores is cryptocrystalline quartz. The chemical composition of the ferromanganese ores in Hazara suggests that the Mn-Fe was contributed by both hydrogenous and hydrothermal sources, while the manganese ores of Waziristan originated only from a hydrothermal source. It is

  3. The Itataia phosphate-uranium deposit (Ceará, Brazil) new petrographic, geochemistry and isotope studies

    NASA Astrophysics Data System (ADS)

    Veríssimo, César Ulisses Vieira; Santos, Roberto Ventura; Parente, Clóvis Vaz; Oliveira, Claudinei Gouveia de; Cavalcanti, José Adilson Dias; Nogueira Neto, José de Araújo

    2016-10-01

    ratios. Mineralized zones exhibit a decrease in δ13C and δ18O isotope values and a higher 87Sr/86Sr ratio toward the center of the vein. In conjunction with petrographic studies, these changes contesting the hypothesis of a sedimentary origin for uranium and suggest a radiogenic Sr input by alkaline to peralkaline fluids from fertile granites of the end of Brasiliano/Pan-African orogeny, located outside the deposit. The origin of the phosphorous is associated with phosphorite deposits in the same depositional environment of the neoproterozoic supracrustal quartz-pelite-carbonate sediments of the Itataia Group. Considering the studies conducted here and available geological data, three main mineralizing events can be identified in Itataia: (1) an initial high temperature event connected with a sodium metasomatism-related uranium episode, taking place in Borborema Province and its African counterpart; (2) a second lower temperature stage, consisting of a multiphase cataclastic/hydrothermal event limited to fault and paleokarst zones; and (3) a third and final event, developed in frankly oxidizing conditions. The last two involving mixing of hydrothermal and meteoric fluids.

  4. Origin of dolomite in the phosphatic Hawthorne Group of Florida

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

    Compton, J.S.; Hall, D.L.; Mallinson, D.J.

    1994-07-01

    In addition to large amounts of phosphorite, the Miocene Hawthorn Group of Florida contains abundant dolomite. Dolomite is present as disseminated silt-size rhombs, as friable dolosilt beds, and as pore-filling cement in dolostone beds and clasts. The dolomite formed during early burial diagenesis both in the sulfate-reduction zone, overlapping and extending below sediment depths of phosphorite formation, and in adjacent, nonphosphatic, shallow-water lagoonal environments. Much of the dolomite is closely associated with the fibrous, Mg-rich clay minerals palygorskite and sepiolite. The percent carbonate in the Hawthorn Group increases from north to south; the dominant carbonate mineral in north Florida ismore » dolomite, whereas dolomite and calcite are both abundant in south Florida. The [delta][sup 13]C values of the dolomite, from +1.82 to [minus]6.21[per thousand] PDB, suggest that metastable biogenic carbonate (aragonite and high-Mg calcite) and seawater were the predominant sources of carbonate. However, negative [delta][sup 13]C values of dolomite from northeast Florida suggest that as much as 30--40% of the carbonate was derived from degradation of organic matter. Degradation of organic matter enhanced dolomitization by removing sulfate ion and increasing the carbonate alkalinity of the pore waters. The oxygen and strontium isotopic values along with moderate Na contents indicate a marine origin. Evaporation of seawater or mixing of seawater and meteoric water were apparently not major factors in dolomite formation. The presence of dolomite, along with phosphorite, in reworked sequences can indicate deposition of organic-rich sediments from which most of the organic matter has since been removed.« less

  5. Seawater as the source of minor elements in black shales, phosphorites and other sedimentary rocks

    USGS Publications Warehouse

    Piper, D.Z.

    1994-01-01

    Many of the minor elements in seawater today have a concentration-depth profile similar to that of the biologically essential nutrients, NO-3 and PO3-4. They show a relative depletion in the photic zone and enrichment in the deep ocean. The difference between their surface- and deep-ocean values, normalized to the change in PO3-4, approaches the average of measured minor-element: P ratios in marine plankton, although individual analyses of the latter show extreme scatter for a variety of reasons. Despite this scatter in the minor-element analyses of plankton, agreement between the two sets of data shows unequivocally that an important marine flux of many minor elements through the ocean is in the form of biogenic matter, with a composition approaching that of plankton. This interpretation is further supported by sediment studies, particularly of sediments which accumulate in shelf-slope environments where biological productivity in the photic zone is exceptionally high and organic carbon contents of the underlying sediment elevated. The interelement relations observed for some of these sediments approach the average values of plankton. These same interelement relations are observed in many marine sedimentary rocks such as metalliferous black shales and phosphorites, rocks which have a high content of marine fractions (e.g., organic matter, apatite, biogenic silica and carbonates). Many previous studies of the geochemistry of these rocks have concluded that local hydrothermal activity, and/or seawater with an elemental content different from that of the modern ocean, was required to account for their minor-element contents. However, the similarity in several of the minor-element ratios in many of these formations to minor-element ratios in modern plankton demonstrates that these sedimentary rocks accumulated in environments whose marine chemistry was virtually identical to that seen on continental shelf-slopes, or in marginal seas, of the ocean today. The

  6. A modern vs. Permian black shale - the hydrography, primary productivity, and water-column chemistry of deposition

    USGS Publications Warehouse

    Piper, D.Z.; Perkins, R.B.

    2004-01-01

    The sediment currently accumulating in the Cariaco Basin, on the continental shelf of Venezuela, has an elevated organic-carbon content of approximately 5%; is accumulating under O2-depleted bottom-water conditions (SO42- reduction); is composed dominantly of foraminiferal calcite, diatomaceous silica, clay, and silt; and is dark greenish gray in color. Upon lithification, it will become a black shale. Recent studies have established the hydrography of the basin and the level of primary productivity and bottom-water redox conditions. These properties are used to model accumulation rates of Cd, Cr, Cu, Mo, Ni, V, and Zn on the seafloor. The model rates agree closely with measured rates for the uppermost surface sediment.The model is applied to the Meade Peak Phosphatic Shale Member of the Phosphoria Formation, a phosphate deposit of Permian age in the northwest United States. It too has all of the requisite properties of a black shale. Although the deposit is a world-class phosphorite, it is composed mostly of phosphatic mudstone and siltstone, chert, limestone, and dolomite. It has organic-carbon concentrations of up to 15%, is strongly enriched in several trace elements above a terrigenous contribution and is black. The trace-element accumulation defines a mean primary productivity in the photic zone of the Phosphoria Basin as moderate, at 500 g m-2 year-1 organic carbon, comparable to primary productivity in the Cariaco Basin. The source of nutrient-enriched water that was imported into the Phosphoria Basin, upwelled into the photic zone, and supported primary productivity was an O2 minimum zone of the open ocean. The depth range over which the water was imported would have been between approximately 100 and 600 m. The mean residence time of bottom water in the basin was approximately 4 years vs. 100 years in the Cariaco Basin. The bottom water was O2 depleted, but it was denitrifying, or NO3- reducing, rather than SO42- reducing. Published by Elsevier B.V.

  7. Preliminary geologic map of the Al Jawf Quadrangle, sheet 29D, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Meissner, C.R.; Dini, S.M.; Farasani, A.M.; Riddler, G.P.; Van Eck, Marcel; Aspinall, N.C.

    1989-01-01

    Phosphorite, a commodity of major economic interest in the Sirhan-Turayf basin, is exposed in the map area along escarpments that form the southeastern rim of the basin. The grade of the phosphorite is as much as 21 percent P2O5, but the beds are thin and lenticular.    

  8. Deposit model for volcanogenic uranium deposits

    USGS Publications Warehouse

    Breit, George N.; Hall, Susan M.

    2011-01-01

    The International Atomic Energy Agency's tabulation of volcanogenic uranium deposits lists 100 deposits in 20 countries, with major deposits in Russia, Mongolia, and China. Collectively these deposits are estimated to contain uranium resources of approximately 500,000 tons of uranium, which amounts to 6 percent of the known global resources. Prior to the 1990s, these deposits were considered to be small (less than 10,000 tons of uranium) with relatively low to moderate grades (0.05 to 0.2 weight percent of uranium). Recent availability of information on volcanogenic uranium deposits in Asia highlighted the large resource potential of this deposit type. For example, the Streltsovskoye district in eastern Russia produced more than 100,000 tons of uranium as of 2005; with equivalent resources remaining. Known volcanogenic uranium deposits within the United States are located in Idaho, Nevada, Oregon, and Utah. These deposits produced an estimated total of 800 tons of uranium during mining from the 1950s through the 1970s and have known resources of 30,000 tons of uranium. The most recent estimate of speculative resources proposed an endowment of 200,000 tons of uranium.

  9. Uranium provinces of North America; their definition, distribution, and models

    USGS Publications Warehouse

    Finch, Warren Irvin

    1996-01-01

    Uranium resources in North America are principally in unconformity-related, quartz-pebble conglomerate, sandstone, volcanic, and phosphorite types of uranium deposits. Most are concentrated in separate, well-defined metallogenic provinces. Proterozoic quartz-pebble conglomerate and unconformity-related deposits are, respectively, in the Blind River–Elliot Lake (BRELUP) and the Athabasca Basin (ABUP) Uranium Provinces in Canada. Sandstone uranium deposits are of two principal subtypes, tabular and roll-front. Tabular sandstone uranium deposits are mainly in upper Paleozoic and Mesozoic rocks in the Colorado Plateau Uranium Province (CPUP). Roll-front sandstone uranium deposits are in Tertiary rocks of the Rocky Mountain and Intermontane Basins Uranium Province (RMIBUP), and in a narrow belt of Tertiary rocks that form the Gulf Coastal Uranium Province (GCUP) in south Texas and adjacent Mexico. Volcanic uranium deposits are concentrated in the Basin and Range Uranium Province (BRUP) stretching from the McDermitt caldera at the Oregon-Nevada border through the Marysvale district of Utah and Date Creek Basin in Arizona and south into the Sierra de Peña Blanca District, Chihuahua, Mexico. Uraniferous phosphorite occurs in Tertiary sediments in Florida, Georgia, and North and South Carolina and in the Lower Permian Phosphoria Formation in Idaho and adjacent States, but only in Florida has economic recovery been successful. The Florida Phosphorite Uranium Province (FPUP) has yielded large quantities of uranium as a byproduct of the production of phosphoric acid fertilizer. Economically recoverable quantities of copper, gold, molybdenum, nickel, silver, thorium, and vanadium occur with the uranium deposits in some provinces.Many major epochs of uranium mineralization occurred in North America. In the BRELUP, uranium minerals were concentrated in placers during the Early Proterozoic (2,500–2,250 Ma). In the ABUP, the unconformity-related deposits were most likely

  10. Economic geology of the Isla de Mona Quadrangle, Puerto Rico

    USGS Publications Warehouse

    Briggs, Reginald Peter

    1974-01-01

    Limiting this tableland In the northern part of Isla de Mona are sheer sea cliffs chiefly exposing the Isla de Mona Dolomite. Around the southern part of the island are Irregular cliffs and steep slopes that chiefly expose the Lirio Limestone. The structure of Isla de Mona consists of two gentle complex folds a broad anticline that trends and plunges gently south-southeast through the central and western parts of Isla de Mona, and a parallel syncline through-the eastern part of the Island that also has a chiefly south-southeast plunge. A near-vertical fault that strikes northwest, then north from the central part to the north coast of Isla de Mona displaces bedrock of the eastern block downward about 10 m. Many caves, including one cave system more than 100,000 m2 in total area, are localized in the lower 10 m of the Lirio Limestone, adjacent to the cliffs peripheral to the upland surface, and numerous small caves occur higher in the Lirio. A few small caves also are found In the Isla de Mona Dolomite. However, the total floor area of all caves on Isla de Mona probably is less than 1 percent of the area of the Island. Almost all caves on Isla de Mona contain phosphorite, which was mined extensively during the late 19th and early 20th centuries. Phosphorite accumulation locally may have exceeded 3.5 m in thickness, but probably averaged less than 1.5 m thick. A fair estimate of original reserves of phosphorite in 12 surveyed caves is about 151,000 m3 of which about 125,500 m3 probably has been removed in mining. Original reserves in the entire island are estimated to have been in the range 158,000 to 235,500 m3. Converted to metric tons, remaining reserves of cave phosphorite probably are considerably less than 50,000. The very pure limestone and calcitic dolomite that form the bedrock of Isla de Mona are abundant industrial-mineral resources. In addition, these carbonate rocks and the beach deposits are sources of construction materials for some classes of

  11. A preliminary evaluation of the nonfuel mineral potential of Somalia

    USGS Publications Warehouse

    Greenwood, W.R.

    1982-01-01

    Additional exploration in Somalia is warranted for a wide variety of metallic and nonmetallic deposits. In Precambrian rocks, deposit types favorable for exploration include: a banded iron formation; platinum-bearing mafic-ultramafic complexes; tin-bearing quartz veins; phosphorite; stratabound base-metal deposits; uranium associated with Precambrian(?) syenite; apatite, molybdenum, and alumina in alkalic rocks; Jurassic and Cretaceous black shales; possible bedded-barite and massive base- and precious-metal sulfide deposits; vein barite in Tertiary rocks in fault zones; sepiolite and bentonite for drilling muds and other industrial uses; celestite; possible Tertiary zeolite; and uranium deposits. Several of these deposit types could be Jointly developed and integrated into domestic industries; for example, phosphate and gypsum, or bentonite for pelletized iron from the banded iron deposits. Other deposits such as barite and sepiolite are of value because of their proximity to major drilling operations in the Arabian Gulf. Still other deposits, such as alumina and banded iron, might be marketable because of proximity to aluminum and iron-refining industries now being constructed in Saudi Arabia. Some deposits, such as celestite, can be developed with little capital investment; others, such as the iron deposits, would require large capital commitments. Exploration and evaluation for many of these deposits can be accomplished by Somali geologists with a few advisors. Most of the deposits require feasibility studies conducted by teams of economic geologists, extractive metallurgists, and economists. Some marginal deposits could be exploited if cooperative development schemes could be negotiated with governments in nearby countries.

  12. Mineral resources of Elko County, Nevada

    USGS Publications Warehouse

    Smith, Roscoe Maurice

    1976-01-01

    Of the 66 named mining districts in Elko County, 56 have been productive of one or more of 19 different commodities: 11 metals--copper, gold, silver, lead, zinc, mercury, tungsten, manganese, iron, uranium, and antimony; 8 nonmetals--sand and gravel, stone, barite, diatomite, gems, oil shale, volcanic ash, and clay. In addition to the commodities produced, at least 5 others--beryllium, molybdenum, tin, phosphorite, and petroleum, occur in amounts sufficient to warrant exploration. The other districts have been explored, but no production has been recorded. Total value-when-sold of production recorded through 1969 was nearly $91 million; actual production was considerably greater, especially if sand and gravel, barite, and other nonmetallic products before 1953 are included. In value of metals produced, the five highest districts are Mountain City ($26 million), Tuscarora ($11 million), Jarbidge ($10 million), Aura ($6 million), and Railroad (nearly $5 million). The Rio Tinto copper mine in the Mountain City district yielded $21 million. Of the 17 districts that produced nonmetallic minerals, Bootstrap .is the largest producer, containing the Rossi mine, one of the two largest barite mines in the United States. Most of /he metals produced name from veins and replacement deposits in limestone or dolomite near granitic stocks; exceptions are manganese and mercury, which are not associated with known or inferred stocks; mercury is further excepted because it occurs in volcanic rocks, as do a few deposits of the major metals. The largest deposit--the Rio Tinto lode--was a combination of fissure filling and replacement along a bedding plane shear zone 150 ft wide and 1,200 ft long in carbonaceous shale of the Valmy Formation; this deposit is apparently older than the Mountain City stock and its mineralization may be related to Paleozoic mafic volcanism later than a major thrust fault, inferred to underlie the area at a depth of about 5,000 ft. Most of the nonmetallic

  13. Oceanographic controls on sedimentary and geochemical facies on the Peru outer shelf and upper slope

    USGS Publications Warehouse

    Arthur, Michael A.; Dean, Walter E.

    2013-01-01

    Concentrations and characteristics of organic matter in surface sediments deposited under an intense oxygen-minimum zone (OMZ) on the Peru margin were mapped and studied in samples from deck-deployed box cores and push cores acquired by submersible on two east-west transects spanning depths of 75 to 1,000 meters (m) at 12°S and 13.5°S. On the basis of sampling and analyses of the top 1–2 centimeters (cm) of available cores, three main belts of sediments were identified on each transect with increasing depth: (1) muds rich in organic carbon (OC); (2) authigenic phosphatic mineral crusts and pavements; and (3) glaucony facies.Sediments rich in OC on the 12°S transect were mainly located on the outer shelf and upper slope (150–350 m), but they occurred in much shallower water (approximately 100 m) on the 13.5°S transect. The organic matter is almost entirely marine as confirmed by Rock-Eval pyrolysis and isotopic composition of OC. Concentrations of OC are highest (up to 18 percent) in sediments within the OMZ where dissolved oxygen (DO) concentrations are <5 micromoles per kilogram (μM). Even at these low concentrations of DO, however, the surface sediments from within the OMZ are dominantly unlaminated. Concentrations of DO may have the dominant effect on organic matter characteristics, but reworking of fine-grained sediment and organic matter by strong bottom currents with velocities as high as 30 centimeters per second (cm/s) on the slope between 150 and 300 m and redeposition on the seafloor in areas of lower energy and higher DO concentration also exert important controls on OC concentration and degree of oxidation in this region.Phosphate-rich sediments and crusts occurred at depths of about 300 to 550 m on both transects. Nodular crusts of sediment cemented by carbonate-fluorapatite (CFA; phosphorite) or dolomite form within the OMZ. These phosphorite crusts evolve through cementation from light olive-green, stiff but friable, phosphatized claystone

  14. U.s. Geological survey core drilling on the atlantic shelf.

    PubMed

    Hathaway, J C; Poag, C W; Valentine, P C; Manheim, F T; Kohout, F A; Bothner, M H; Miller, R E; Schultz, D M; Sangrey, D A

    1979-11-02

    The first broad program of scientific shallow drilling on the U.S. Atlantic continental shelf has delineated rocks of Pleistocene to Late Cretaceous age, including phosphoritic Miocene strata, widespread Eocene carbonate deposits that serve as reflective seismic markers, and several regional unconformities. Two sites, off Maryland and New Jersey, showed light hydrocarbon gases having affinity to mature petroleum. Pore fluid studies showed that relatively fresh to brackish water occurs beneath much of the Atlantic continental shelf, whereas increases in salinity off Georgla and beneath the Florida-Hatteras slope suggest buried evaporitic strata. The sediment cores showed engineering properties that range from good foundation strength to a potential for severe loss of strength through interaction between sediments and man-made structures.

  15. Mineralogical characterization of strata of the Meade Peak phosphatic shale member of the Permian Phosphoria Formation: channel and individual rock samples of measured section J and their relationship to measured sections A and B, central part of Rasmussen Ridge, Caribou County, Idaho

    USGS Publications Warehouse

    Knudsen, A.C.; Gunter, M.E.; Herring, J.R.; Grauch, R.I.

    2002-01-01

    The Permian Phosphoria Formation of southeastern Idaho hosts one of the largest phosphate deposits in the world. Despite the economic significance of this Formation, the fine-grained nature of the phosphorite has discouraged detailed mineralogical characterization and quantification studies. Recently, selenium and other potentially toxic trace elements in mine wastes have drawn increased attention to this formation, and motivated additional study. This study uses powder X-ray diffraction (XRD), with Rietveld quantification software, to quantify and characterize the mineralogy of composite channel samples and individual samples collected from the stratigraphic sections measured by the U.S. Geological Survey in the Meade Peak Member of the Permian Phosphoria Formation at the Enoch Valley mine on Rasmussen Ridge, approximately 15 miles northeast of Soda Springs, Idaho.

  16. 20 CFR 703.207 - Kinds of negotiable securities that may be deposited; conditions of deposit; acceptance of deposits.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... amount fixed by the Office under the regulations in this part shall deposit any negotiable securities... deposited; conditions of deposit; acceptance of deposits. 703.207 Section 703.207 Employees' Benefits... AND RELATED STATUTES INSURANCE REGULATIONS Insurance Carrier Security Deposit Requirements § 703.207...

  17. Geochemistry of Israeli oil shales - A review

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

    Shirav, M.; Ginzbury, D.

    1983-02-01

    The oil shales in Israel are widely distributed throughout the country. Outcrops are rare and the information is based on boreholes data. The oil shale sequence is of UpperCampanian - Maastrichtian age and belongs to the Chareb Formation. In places, part of the phosphorite layer below the oil shales is also rich in kerogen. The host rocks are biomicritic limestones and marls, in which the organic matter is generally homogeneously and finely dispersed. The occurrence of authigenic feldspar and the preservation of the organic matter (up to 26% of the total rock) indicate euxinic hypersaline conditions which prevailed in themore » relative closed basins of deposition during the Maastrichtian. Current reserves of oil shales in Israel are about 3,500 million tons, located in the following deposits: Zin, Oron, Ef'e, Hartuv and Nabi-Musa. The 'En Bokek deposit, although thoroughly investigated, is of limited reserves and is not considered for future exploitation. Other potential areas, in the Northern Negev and along the Coastal Plain are under investigation. Future successful utilization of the Israeli oil shales, either by fluidizid-bed combustion or by retorting will contribute to the state's energy balance.« less

  18. Cobalt—Styles of deposits and the search for primary deposits

    USGS Publications Warehouse

    Hitzman, Murray W.; Bookstrom, Arthur A.; Slack, John F.; Zientek, Michael L.

    2017-11-30

    Cobalt (Co) is a potentially critical mineral. The vast majority of cobalt is a byproduct of copper and (or) nickel production. Cobalt is increasingly used in magnets and rechargeable batteries. More than 50 percent of primary cobalt production is from the Central African Copperbelt. The Central African Copperbelt is the only sedimentary rock-hosted stratiform copper district that contains significant cobalt. Its presence may indicate significant mafic-ultramafic rocks in the local basement. The balance of primary cobalt production is from magmatic nickel-copper and nickel laterite deposits. Cobalt is present in several carbonate-hosted lead-zinc and copper districts. It is also variably present in Besshi-type volcanogenic massive sulfide and siliciclastic sedimentary rock-hosted deposits in back arc and rift environments associated with mafic-ultramafic rocks. Metasedimentary cobalt-copper-gold deposits (such as Blackbird, Idaho), iron oxide-copper-gold deposits, and the five-element vein deposits (such as Cobalt, Ontario) contain different amounts of cobalt. None of these deposit types show direct links to mafic-ultramafic rocks; the deposits may result from crustal-scale hydrothermal systems capable of leaching and transporting cobalt from great depths. Hydrothermal deposits associated with ultramafic rocks, typified by the Bou Azzer district of Morocco, represent another type of primary cobalt deposit.In the United States, exploration for cobalt deposits may focus on magmatic nickel-copper deposits in the Archean and Proterozoic rocks of the Midwest and the east coast (Pennsylvania) and younger mafic rocks in southeastern and southern Alaska; also, possibly basement rocks in southeastern Missouri. Other potential exploration targets include—The Belt-Purcell basin of British Columbia (Canada), Idaho, Montana, and Washington for different styles of sedimentary rock-hosted cobalt deposits;Besshi-type VMS deposits, such as the Greens Creek (Alaska) deposit and

  19. Airfoil deposition model

    NASA Technical Reports Server (NTRS)

    Kohl, F. J.

    1982-01-01

    The methodology to predict deposit evolution (deposition rate and subsequent flow of liquid deposits) as a function of fuel and air impurity content and relevant aerodynamic parameters for turbine airfoils is developed in this research. The spectrum of deposition conditions encountered in gas turbine operations includes the mechanisms of vapor deposition, small particle deposition with thermophoresis, and larger particle deposition with inertial effects. The focus is on using a simplified version of the comprehensive multicomponent vapor diffusion formalism to make deposition predictions for: (1) simple geometry collectors; and (2) gas turbine blade shapes, including both developing laminar and turbulent boundary layers. For the gas turbine blade the insights developed in previous programs are being combined with heat and mass transfer coefficient calculations using the STAN 5 boundary layer code to predict vapor deposition rates and corresponding liquid layer thicknesses on turbine blades. A computer program is being written which utilizes the local values of the calculated deposition rate and skin friction to calculate the increment in liquid condensate layer growth along a collector surface.

  20. Security Deposits

    DTIC Science & Technology

    1987-04-01

    security deposit action is described in the regulation as follows: h. Security Deposits (DACF and DACA ). (1) Issue. PCS moves create financial hardships...General Wickham, The Army Chief of Staff, specified a philosophy toward the family in the Army Family White Paper. General Wickham’s action was in...security deposits arose. 1 The Army’s action to the issue of security deposits will be thoroughly discussed in this paper. The Army’s action comes now

  1. 20 CFR 703.306 - Kinds of negotiable securities that may be deposited; conditions of deposit; acceptance of deposits.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... AND RELATED STATUTES INSURANCE REGULATIONS Authorization of Self-Insurers § 703.306 Kinds of negotiable securities that may be deposited; conditions of deposit; acceptance of deposits. A self-insurer or a self-insurer applicant electing to deposit negotiable securities to secure its obligations under...

  2. Sediment-Hosted Copper Deposits of the World: Deposit Models and Database

    USGS Publications Warehouse

    Cox, Dennis P.; Lindsey, David A.; Singer, Donald A.; Diggles, Michael F.

    2003-01-01

    Introduction This publication contains four descriptive models and four grade-tonnage models for sediment hosted copper deposits. Descriptive models are useful in exploration planning and resource assessment because they enable the user to identify deposits in the field and to identify areas on geologic and geophysical maps where deposits could occur. Grade and tonnage models are used in resource assessment to predict the likelihood of different combinations of grades and tonnages that could occur in undiscovered deposits in a specific area. They are also useful in exploration in deciding what deposit types meet the economic objectives of the exploration company. The models in this report supersede the sediment-hosted copper models in USGS Bulletin 1693 (Cox, 1986, and Mosier and others, 1986) and are subdivided into a general type and three subtypes. The general model is useful in classifying deposits whose features are obscured by metamorphism or are otherwise poorly described, and for assessing regions in which the geologic environments are poorly understood. The three subtypes are based on differences in deposit form and environments of deposition. These differences are described under subtypes in the general model. Deposit models are based on the descriptions of geologic environments and physical characteristics, and on metal grades and tonnages of many individual deposits. Data used in this study are presented in a database representing 785 deposits in nine continents. This database was derived partly from data published by Kirkham and others (1994) and from new information in recent publications. To facilitate the construction of grade and tonnage models, the information, presented by Kirkham in disaggregated form, was brought together to provide a single grade and a single tonnage for each deposit. Throughout the report individual deposits are defined as being more than 2,000 meters from the nearest adjacent deposit. The deposit models are presented here as

  3. Regional analysis of spiculite faunas in the permian phosphoria basin: Implications for paleoceanography

    USGS Publications Warehouse

    Murchey, Benita L.

    2004-01-01

    During the Permian, the relative abundance and apparent diversity of siliceous sponges expanded over a wide range of depths in the basins from Nevada and Idaho to the open ocean. Radiolarian preservation and apparent diversity increased in the deeper Cordilleran basins as well. In the Arctic regions, significant sponge spiculites were deposited in epicratonic basins. At the same time that siliceous sponge populations expanded along the northwestern margin of Pangea, warm-water carbonate producers disappeared. Suppression of carbonate-producing organisms along the margin was critical to the accu- mulation and preservation of both the demosponge spiculites in the Eastern Belt and the spicule-rich argillites of the Central Belt. Vigorous thermohaline circulation was the major control on the paleobiogeography of the late Early, Middle, and early Late Permian along northwest Pangea. It was driven by cold, nutrient- and oxygen-rich northern waters and it produced a coastal current that swept down the margin of the supercontinent. The upwelling associated with deposition of world-class phosphorites in the Phosphoria basin was a part of this larger oceanographic system.

  4. Porphyry copper deposit density

    USGS Publications Warehouse

    Singer, Donald A.; Berger, Vladimir; Menzie, W. David; Berger, Byron R.

    2005-01-01

    Estimating numbers of undiscovered mineral deposits has been a source of unease among economic geologists yet is a fundamental task in considering future supplies of resources. Estimates can be based on frequencies of deposits per unit of permissive area in control areas around the world in the same way that grade and tonnage frequencies are models of sizes and qualities of undiscovered deposits. To prevent biased estimates it is critical that, for a particular deposit type, these deposit density models be internally consistent with descriptive and grade and tonnage models of the same type. In this analysis only deposits and prospects that are likely to be included in future grade and tonnage models are employed, and deposits that have mineralization or alteration separated by less than an arbitrary but consistent distance—2 km for porphyry copper deposits—are combined into one deposit. Only 286 deposits and prospects that have more than half of the deposit not covered by postmineral rocks, sediments, or ice were counted.Nineteen control areas were selected and outlined along borders of hosting magmatic arc terranes based on three main features: (1) extensive exploration for porphyry copper deposits, (2) definable geologic settings of the porphyry copper deposits in island and continental volcanic-arc subduction-boundary zones, and (3) diversity of epochs of porphyry copper deposit formation.Porphyry copper deposit densities vary from 2 to 128 deposits per 100,000 km2 of exposed permissive rock, and the density histogram is skewed to high values. Ninety percent of the control areas have densities of four or more deposits, 50 percent have densities of 15 or more deposits, and 10 percent have densities of 35 or more deposits per 100,000 km2. Deposit density is not related to age or depth of emplacement. Porphyry copper deposit density is inversely related to the exposed area of permissive rock. The linear regression line and confidence limits constructed with

  5. What controls deposition rate in electron-beam chemical vapor deposition?

    PubMed

    White, William B; Rykaczewski, Konrad; Fedorov, Andrei G

    2006-08-25

    The key physical processes governing electron-beam-assisted chemical vapor deposition are analyzed via a combination of theoretical modeling and supporting experiments. The scaling laws that define growth of the nanoscale deposits are developed and verified using carefully designed experiments of carbon deposition from methane onto a silicon substrate. The results suggest that the chamber-scale continuous transport of the precursor gas is the rate controlling process in electron-beam chemical vapor deposition.

  6. Environmental significance of Upper Miocene phosphorites at hominid sites in the Lukeino Formation (Tugen Hills, Kenya)

    NASA Astrophysics Data System (ADS)

    Dericquebourg, Perrine; Person, Alain; Ségalen, Loïc; Pickford, Martin; Senut, Brigitte; Fagel, Nathalie

    2015-08-01

    The Lukeino Formation contains an important sedimentary and fossiliferous record of the late Miocene (6.09-5.68 Ma), which has in particular yielded the fossil remains of the oldest East African bipedal hominid called Orrorin tugenensis. This fluvio-lacustrine sedimentary succession crops out in the Kenyan part of the East African Rift. It is mainly composed of clay to sandy clay deposits intercalated with volcanic ash horizons, and localized layers of carbonates and diatomites. A detailed sedimentological and mineralogical study of the Lukeino Formation was conducted to throw light on the environmental conditions in which the hominids lived. Several centimetric, relatively continuous and indurated phosphatic horizons, of sedimentary origin, were identified at two sites (Sunbarua and Kapcheberek). Mineralogical (XRD) and geochemical analyses as well as observations by SEM, which was coupled with an energy dispersive spectroscopy (EDS) microprobe, indicate that the autochthonous phosphate layers are composed of a micritic matrix of francolite (38-93%), with incorporation of silicates in variable proportions from one layer to another. The phosphate matrix contains very well preserved and abundant diatom frustules in the basal phosphate layer. These diatoms are identified as Aulacoseira granulata, implying a pH of 7.8-8.2 for freshwaters of the Palaeolake Lukeino. Calcitic tubular structures, linked to a possible bacterial origin, are also observed locally. Phosphate layers occur abruptly within a thick clay-sandy series, associated with an intense runoff phase during the deposition of this interval of the Lukeino Formation. The massive and cyclic input of phosphorus to the lake promoted productivity to the stage where it caused a diatom bloom. The establishment of several phosphate horizons testifies to successive phases of eutrophication of Palaeolake Lukeino. The diatom cells provided some of the organic matter, which was decomposed by bacterial activity at the

  7. DepositScan, a Scanning Program to Measure Spray Deposition Distributions

    USDA-ARS?s Scientific Manuscript database

    DepositScan, a scanning program was developed to quickly measure spray deposit distributions on water sensitive papers or Kromekote cards which are widely used for determinations of pesticide spray deposition quality on target areas. The program is installed in a portable computer and works with a ...

  8. Lithofacies, Age, and Sequence Stratigraphy of the Carboniferous Lisburne Group in the Skimo Creek Area, Central Brooks Range

    USGS Publications Warehouse

    Dumoulin, Julie A.; Whalen, Michael T.; Harris, Anita G.

    2008-01-01

    The Lisburne Group, a mainly Carboniferous carbonate succession that is widely distributed across northern Alaska, contains notable amounts of oil and gas at Prudhoe Bay. Detailed studies of the Lisburne in the Skimo Creek area, central Brooks Range, delineate its lithofacies, age, conodont biofacies, depositional environments, and sequence stratigraphy and provide new data on its hydrocarbon source-rock and reservoir potential, as well as its thermal history, in this area. We have studied the Lisburne Group in two thrust sheets of the Endicott Mountains allochthon, herein called the Skimo and Tiglukpuk thrust sheets. The southern, Skimo Creek section, which is >900 m thick, is composed largely of even-bedded to nodular lime mudstone and wackestone intercalated with intervals of thin- to thick-bedded bioclastic packstone and grainstone. Some parts of the section are partially to completely dolomitized and (or) replaced by chert. A distinctive, 30-m-thick zone of black, organic-rich shale, lime mudstone, and phosphorite is exposed 170 m below the top of the Lisburne. The uppermost 40 m of section is also distinctive and made up of dark shale, lime mudstone, spiculite, and glauconitic grainstone. The northern, Tiglukpuk Creek section, which is similar to the Skimo Creek section but only ~760 m thick, includes more packstone and grainstone and less organic-rich shale. Analyses of conodonts and foraminifers indicate that both sections range in age from late Early Mississippian (Osagean) through Early Pennsylvanian (early Morrowan) and document a hiatus of at least 15 m.y. at the contact between the Lisburne and the overlying Siksikpuk Formation. No evidence of subaerial exposure was observed along this contact, which may represent a submarine erosional surface. Lithofacies and biofacies imply that the Lisburne Group in the study area was deposited mainly in midramp to outer-ramp settings. Deepest water strata are mud rich and formed below storm or fair-weather wave

  9. 78 FR 56583 - Deposit Insurance Regulations; Definition of Insured Deposit

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-09-13

    ... as a potential global deposit insurer, preserve confidence in the FDIC deposit insurance system, and... the United States.\\2\\ The FDIC generally pays out deposit insurance on the next business day after a... since 2001 and total approximately $1 trillion today. In many cases, these branches do not engage in...

  10. Deposition of Boron in Possible Evaporite Deposits in Gale Crate

    NASA Astrophysics Data System (ADS)

    Gasda, P. J.; Peets, E.; Lamm, S. N.; Rapin, W.; Lanza, N.; Frydenvang, J.; Clark, B. C.; Herkenhoff, K. E.; Bridges, J.; Schwenzer, S. P.; Haldeman, E. B.; Wiens, R. C.; Maurice, S.; Clegg, S. M.; Delapp, D.; Sanford, V.; Bodine, M. R.; McInroy, R.

    2017-12-01

    Boron has been previously detected in Gale crater using the ChemCam instrument on board the NASA Curiosity rover within calcium sulfate fracture fill hosted by lacustrine mudstone and eolian sandstone units. Recent results show that up to 300 ppm B is present in the upper sections of the lacustrine unit. Boron has been detected in both the groundwater-emplaced calcium sulfate fracture fill materials and bedding-parallel calcium sulfate layers. The widespread bedding-parallel calcium sulfate layers within the upper strata of the lacustrine bedrock that Curiosity has encountered recently could be interpreted as primary evaporite deposits. We have two hypotheses for the history of boron in Gale crater. In both hypotheses, borates were first deposited as lake water evaporated, depositing primary evaporates that were later re-dissolved by groundwater, which redistributed the boron into secondary evaporitic calcium sulfate fracture fill deposits. In the first scenario, Gale crater may have undergone a period of perennial lake formation during a drier period of martian history, depositing layers of evaporitic minerals (including borates) among lacustrine mudstone layers. In the second scenario, lake margins could have become periodically exposed during cyclic drops in lake level and subsequently desiccated. Evaporites were deposited and desiccation features were formed in lowstand deposits. Either hypothetical scenario of evaporite deposition would promote prebiotic chemical reactions via wet-dry cycles. Boron may be an important prebiotic element, and as such, its presence in ancient martian surface and groundwater provides evidence that important prebiotic chemical reactions could occur on Mars if organics were present. The presence of boron in ancient Gale crater groundwater also provides additional evidence that a habitable environment existed in the martian subsurface well after the expected disappearance of liquid water on the surface of Mars. We will report on the

  11. The Peru Margin as an Authigenic Mineral Factory, Evidence From Surface Sediments and Oceanography

    NASA Astrophysics Data System (ADS)

    Dean, W. E.; Arthur, M. A.

    2004-12-01

    Characteristics of sediments deposited within an intense oxygen-minimum zone (OMZ) on the Peru continental margin were mapped by submersible, and studied in samples collected in deck-deployed box cores and submersible push cores on two east-west transects over water depths of 75 to 1000 m at 12 degrees and 13.5 degrees S. On the basis of sampling of the top 1-2 cm of available cores, three main belts of sediments were identified in each transect with increasing depth: 1) organic-carbon (OC)-rich muds; 2) authigenic phosphatic mineral crusts; and 3) glaucony facies. These facies patterns are primarily controlled by redox conditions and strength of bottom currents. OC-rich sediments on the 12-degree transect were mainly located on the outer shelf and upper slope (150-350 m), but they occurred in much shallower water (ca. 100 m) on the 13.5-degree transect. The organic matter is almost entirely marine, resulting from very high primary productivity. The OC concentrations are highest (up to 18%) in sediments where intermediate water masses with low dissolved oxygen concentrations (less than 5 micromoles/kg) impinge on the slope at water depths between 75 and 450 m. The region between 175 and 350 m depth is characterized by bedforms stabilized by bacterial mats, extensive authigenic mineral crusts, and (or) thick organic flocs. Currents as high as 30 cm/sec were measured over that depth interval. Current-resuspension of surficial organic matter, activity of organisms, and transport to and from more oxygenated zones contribute to greater oxidation and poorer preservation of organic matter than occur under oxygen-deficient conditions. Phosphate-rich sediments occurred at depths of about 300 to 550 m on both transects. Nodular crusts cemented by carbonate-fluorapatite (CFA; phosphorite) or dolomite form within the OMZ. The crusts start by cementation of sediment near the sediment-water interface forming stiff but friable phosphatizes claystone "protocrusts". The protocrusts

  12. Growth and dielectric properties of ZnO nanoparticles deposited by using electrophoretic deposition

    NASA Astrophysics Data System (ADS)

    Chung, Yoonsung; Park, Hyejin; Kim, Dong-Joo; Cho, Sung Baek; Yoon, Young Soo

    2015-05-01

    The deposition behavior of ZnO nanoparticles on metal plates and conductive fabrics was investigated using electrophoretic deposition (EPD). The deposition kinetics on both metal plates and fabrics were examined using the Hamaker equation. Fabric substrates give more deposited weight than flat substrates due to their rougher shape and higher surface area. The morphologies and the structures of the deposited ZnO layers showed uniform deposition without any preferred orientation on both substrates. The dielectric properties of the ZnO layers formed by using EPD showed values that were reduced, but comparable to those of bulk ZnO. This result suggests that EPD is a convenient method to deposit functional oxides on flexible substrates.

  13. Solution deposition assembly

    DOEpatents

    Roussillon, Yann; Scholz, Jeremy H; Shelton, Addison; Green, Geoff T; Utthachoo, Piyaphant

    2014-01-21

    Methods and devices are provided for improved deposition systems. In one embodiment of the present invention, a deposition system is provided for use with a solution and a substrate. The system comprises of a solution deposition apparatus; at least one heating chamber, at least one assembly for holding a solution over the substrate; and a substrate curling apparatus for curling at least one edge of the substrate to define a zone capable of containing a volume of the solution over the substrate. In another embodiment of the present invention, a deposition system for use with a substrate, the system comprising a solution deposition apparatus; at heating chamber; and at least assembly for holding solution over the substrate to allow for a depth of at least about 0.5 microns to 10 mm.

  14. Multi-chamber deposition system

    DOEpatents

    Jacobson, Richard L.; Jeffrey, Frank R.; Westerberg, Roger K.

    1989-10-17

    A system for the simultaneous deposition of different coatings onto a thin web within a large volume vacuum chamber is disclosed which chamber is provided with a plurality of deposition chambers in which the different layers are deposited onto the film as its moves from a supply roll to a finished take-up roll of coated web. The deposition chambers provided within the large vacuum chamber are provided with separate seals which minimize back diffusion of any dopant gas from adjacent deposition chambers.

  15. Multi-chamber deposition system

    DOEpatents

    Jacobson, Richard L.; Jeffrey, Frank R.; Westerberg, Roger K.

    1989-06-27

    A system for the simultaneous deposition of different coatings onto a thin web within a large volume vacuum chamber is disclosed which chamber is provided with a plurality of deposition chambers in which the different layers are deposited onto the film as its moves from a supply roll to a finished take-up roll of coated web. The deposition chambers provided within the large vacuum chamber are provided with separate seals which minimize back diffusion of any dopant gas from adjacent deposition chambers.

  16. MAPLE deposition of nanomaterials

    NASA Astrophysics Data System (ADS)

    Caricato, A. P.; Arima, V.; Catalano, M.; Cesaria, M.; Cozzoli, P. D.; Martino, M.; Taurino, A.; Rella, R.; Scarfiello, R.; Tunno, T.; Zacheo, A.

    2014-05-01

    The matrix-assisted pulsed laser evaporation (MAPLE) has been recently exploited for depositing films of nanomaterials by combining the advantages of colloidal inorganic nanoparticles and laser-based techniques. MAPLE-deposition of nanomaterials meeting applicative purposes demands their peculiar properties to be taken into account while planning depositions to guarantee a congruent transfer (in terms of crystal structure and geometric features) and explain the deposition outcome. In particular, since nanofluids can enhance thermal conductivity with respect to conventional fluids, laser-induced heating can induce different ablation thermal regimes as compared to the MAPLE-treatment of soft materials. Moreover, nanoparticles exhibit lower melting temperatures and can experience pre-melting phenomena as compared to their bulk counterparts, which could easily induce shape and or crystal phase modification of the material to be deposited even at very low fluences. In this complex scenario, this review paper focuses on examples of MAPLE-depositions of size and shape controlled nanoparticles for different applications highlights advantages and challenges of the MAPLE-technique. The influence of the deposition parameters on the physical mechanisms which govern the deposition process is discussed.

  17. Trouvelot Crater Deposit

    NASA Image and Video Library

    2002-12-04

    Like many of the craters in the Oxia Palus region of Mars, Trouvelot Crater, shown in this NASA Mars Odyssey image, hosts an eroded, light-toned, sedimentary deposit on its floor. Compared with the much larger example in Becquerel Crater to the NE, the Trouvelot deposit has been so eroded by the scouring action of dark, wind-blown sand that very little of it remains. Tiny outliers of bright material separated from the main mass attest to the once, more really extensive coverage by the deposit. A similar observation can be made for White Rock, the best known example of a bright, crater interior deposit. The origin of the sediments in these deposits remains enigmatic but they are likely the result of fallout from ash or dust carried by the thin martian atmosphere. http://photojournal.jpl.nasa.gov/catalog/PIA04017

  18. Sediment-hosted stratabound copper deposit model: Chapter M in Mineral deposit model for resource assessment

    USGS Publications Warehouse

    Hayes, Timothy S.; Cox, Dennis P.; Bliss, James D.; Piatak, Nadine M.; Seal, Robert R.

    2015-01-01

    This report contains a descriptive model of sediment-hosted stratabound copper (SSC) deposits that supersedes the model of Cox and others (2003). This model is for use in assessments of mineral resource potential. SSC deposits are the second most important sources of copper in the world behind porphyry copper deposits. Around 20 percent of the copper in the world is produced from this class of deposits. They are also the most important sources of cobalt in the world, and they are fourth among classes of ore deposits in production of silver. SSC deposits are the basis of the economies of three countries: Democratic Republic of Congo, Poland, and Zambia. This report provides a description of the key features of SSC deposits; it identifies their tectonic-sedimentary environments; it illustrates geochemical, geophysical, and geoenvironmental characteristics of SSC deposits; it reviews and evaluates hypotheses on how these deposits formed; it presents exploration and assessment guides; and it lists some gaps in our knowledge about the SSC deposits. A summary follows that provides overviews of many subjects concerning SSC deposits.

  19. 29 CFR 2200.56 - Depositions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... deposition shall be taken in accordance with the Federal Rules of Civil Procedure, particularly Federal Rule... dismiss. (c) Notice of taking. Any depositions allowed by the Commission or Judge may be taken after 10... borne by the party at whose instance the deposition is taken. (e) Use of depositions. Depositions taken...

  20. 29 CFR 2200.56 - Depositions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... deposition shall be taken in accordance with the Federal Rules of Civil Procedure, particularly Federal Rule... dismiss. (c) Notice of taking. Any depositions allowed by the Commission or Judge may be taken after 10... borne by the party at whose instance the deposition is taken. (e) Use of depositions. Depositions taken...

  1. 24 CFR 26.20 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 24 Housing and Urban Development 1 2011-04-01 2011-04-01 false Depositions. 26.20 Section 26.20... PROCEDURES Hearings Before Hearing Officers Discovery § 26.20 Depositions. (a) Taking oral deposition. A party may take the oral deposition of any person. Reasonable written notice of deposition shall be...

  2. 24 CFR 26.20 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 24 Housing and Urban Development 1 2010-04-01 2010-04-01 false Depositions. 26.20 Section 26.20... PROCEDURES Hearings Before Hearing Officers Discovery § 26.20 Depositions. (a) Taking oral deposition. A party may take the oral deposition of any person. Reasonable written notice of deposition shall be...

  3. Ionized cluster beam deposition

    NASA Technical Reports Server (NTRS)

    Kirkpatrick, A. R.

    1983-01-01

    Ionized Cluster Beam (ICB) deposition, a new technique originated by Takagi of Kyoto University in Japan, offers a number of unique capabilities for thin film metallization as well as for deposition of active semiconductor materials. ICB allows average energy per deposited atom to be controlled and involves impact kinetics which result in high diffusion energies of atoms on the growth surface. To a greater degree than in other techniques, ICB involves quantitative process parameters which can be utilized to strongly control the characteristics of films being deposited. In the ICB deposition process, material to be deposited is vaporized into a vacuum chamber from a confinement crucible at high temperature. Crucible nozzle configuration and operating temperature are such that emerging vapor undergoes supercondensation following adiabatic expansion through the nozzle.

  4. Mechanical characteristics of a tool steel layer deposited by using direct energy deposition

    NASA Astrophysics Data System (ADS)

    Baek, Gyeong Yun; Shin, Gwang Yong; Lee, Eun Mi; Shim, Do Sik; Lee, Ki Yong; Yoon, Hi-Seak; Kim, Myoung Ho

    2017-07-01

    This study focuses on the mechanical characteristics of layered tool steel deposited using direct energy deposition (DED) technology. In the DED technique, a laser beam bonds injected metal powder and a thin layer of substrate via melting. In this study, AISI D2 substrate was hardfaced with AISI H13 and M2 metal powders for mechanical testing. The mechanical and metallurgical characteristics of each specimen were investigated via microstructure observation and hardness, wear, and impact tests. The obtained characteristics were compared with those of heat-treated tool steel. The microstructures of the H13- and M2-deposited specimens show fine cellular-dendrite solidification structures due to melting and subsequent rapid cooling. Moreover, the cellular grains of the deposited M2 layer were smaller than those of the H13 structure. The hardness and wear resistance were most improved in the M2-deposited specimen, yet the H13-deposited specimen had higher fracture toughness than the M2-deposited specimen and heat-treated D2.

  5. An automatic collector to monitor insoluble atmospheric deposition: application for mineral dust deposition

    NASA Astrophysics Data System (ADS)

    Laurent, B.; Losno, R.; Chevaillier, S.; Vincent, J.; Roullet, P.; Bon Nguyen, E.; Ouboulmane, N.; Triquet, S.; Fornier, M.; Raimbault, P.; Bergametti, G.

    2015-07-01

    Deposition is one of the key terms of the mineral dust cycle. However, dust deposition remains poorly constrained in transport models simulating the atmospheric dust cycle. This is mainly due to the limited number of relevant deposition measurements. This paper aims to present an automatic collector (CARAGA), specially developed to sample the total (dry and wet) atmospheric deposition of insoluble dust in remote areas. The autonomy of the CARAGA can range from 25 days to almost 1 year depending on the programmed sampling frequency (from 1 day to 2 weeks respectively). This collector is used to sample atmospheric deposition of Saharan dust on the Frioul islands in the Gulf of Lions in the Western Mediterranean. To quantify the mineral dust mass in deposition samples, a weighing and ignition protocol is applied. Almost 2 years of continuous deposition measurements performed on a weekly sampling basis on Frioul Island are presented and discussed with air mass trajectories and satellite observations of dust. Insoluble mineral deposition measured on Frioul Island was 2.45 g m-2 for February to December 2011 and 3.16 g m-2 for January to October 2012. Nine major mineral deposition events, measured during periods with significant MODIS aerosol optical depths, were associated with air masses coming from the southern Mediterranean Basin and North Africa.

  6. 49 CFR 386.46 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 5 2011-10-01 2011-10-01 false Depositions. 386.46 Section 386.46 Transportation... and Hearings § 386.46 Depositions. (a) When, how, and by whom taken. (1) The deposition of any witness... accordance with § 386.37, for leave to conduct a deposition based on good cause shown. (2) Depositions may be...

  7. 49 CFR 386.46 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 5 2010-10-01 2010-10-01 false Depositions. 386.46 Section 386.46 Transportation... and Hearings § 386.46 Depositions. (a) When, how, and by whom taken. (1) The deposition of any witness... accordance with § 386.37, for leave to conduct a deposition based on good cause shown. (2) Depositions may be...

  8. Physical deposit measures and commercial potential: The case of titanium-bearing heavy-mineral deposits

    USGS Publications Warehouse

    Attanasi, E.D.; DeYoung, J.H.

    1988-01-01

    Physical measures of mineral deposit characteristics, such as grade and tonnage, long have been used in both subjective and analytic models to predict favorability of areas for the occurrence of mineral deposits of particular types. After a deposit has been identified, however, the explorationist must decide whether to continue data collection, begin an economic feasibility study, or abandon the prospect. The decision maker can estimate the probability that a deposit will be commercial by examining physical measures. The amount of sampling data required before such a probability estimate can be considered reliable can be determined. A logit probability model estimated from onshore titanium-bearing heavy-mineral deposit data identifies and quantifies the relative influence of a deposit's physical measures on the chances of the deposit becoming commercial. A principal conclusion that can be drawn from the analysis is that, along with a measure of deposit size, the characteristics most important in predicting commercial potential are grades of the constituent minerals. Total heavy-mineral-bearing sand grade or even total titanium grade (without data on constituent mineral grades) are poor predictors of the deposit's commercial potential. ?? 1988 International Association for Mathematical Geology.

  9. Phosphorus in the ocean and marine sediments: similarities between present and past processes

    NASA Astrophysics Data System (ADS)

    Tamburini, F.

    2004-12-01

    Because phosphorus (P) is an essential nutrient, geochemical research has focused over the years on understanding the different aspects of the P cycle in the oceans, from the global to microbial scale. In the last 40 years, giant phosphorite deposits were largely studied, and their episodic occurrence in the geological record was alternatively interpreted as the product of shallow water environments, high productivity, low-sedimentation rates, and/or changes in sea level. Although research has focused more recently on the oceanic burial fluxes and residence time of P, there is still a general agreement on the need for more data. Thanks to new analytical techniques, allowing the detection of small quantities of phosphate (on the order of ?mol/g), and to the increased availability of sediment cores, P-bearing sediments have been found everywhere beneath the ocean floor. This finding has changed our understanding of P behavior in the ocean, and is redefining the role of P as an important nutrient, for example, over glacial-interglacial time scales. I will present glacial-interglacial reconstructions of burial and benthic fluxes of P, with the goal of understanding to which extent the P cycle is linked to global processes. The data, averaged to the whole ocean, indicate that burial fluxes of reactive P during glacial times are not considerably lower than during interglacials. This observation could lead to the conclusion that no changes occurred in P cycle on glacial-interglacial timescales and, therefore, that C cycle and climate variations were independent of P cycle. However, when the benthic flux estimates are taken into account, a different picture arises. During low sea level periods, the redistribution of sediments from shallow to deep waters, due to the reduction of the continental margin surface, fostered P regeneration during settling of organic matter. Even if P burial fluxes remain fairly constant, the oceanic phosphate inventory of glacial bottom waters

  10. Sedimentary Deposits within Ius Chasma

    NASA Image and Video Library

    2015-07-15

    Sedimentary deposits are common within Valles Marineris. Most larger chasmata contain kilometer-thick light-toned layered deposits composed of sulfates. However, some of the chasmata, like Ius Chasma shown in this image from NASA Mars Reconnaissance Orbiter, lack these deposits or have much thinner deposits. The light-toned deposits in Ius Chasma are observed both along the floor and inner wallrock materials. Some of the light-toned deposits appear to post-date formation of the chasma floor, whereas other deposits appear to lie beneath wallrock materials, indicating they are older. By examining the stratigraphy using digital terrain models and 3D images, it should be possible to decipher the relative ages of the different geologic units. CRISM data may also provide insight into the mineralogy, which will tell scientists about the aqueous conditions that emplaced the light-toned deposits. http://photojournal.jpl.nasa.gov/catalog/PIA19855

  11. Mineral deposits of Central America, with a section on manganese deposits of Panama

    USGS Publications Warehouse

    Roberts, Ralph Jackson; Irving, Earl Montgomery; Simons, F.S.

    1957-01-01

    The mineral deposits of Central America were studied between 1942 and 1945, in cooperation with the United States Department of State and the Foreign Economic Administration. Emphasis was originally placed on the study of strategic-mineral deposits, especially of antimony, chromite, manganese, quartz, and mica, but deposits of other minerals that offered promise of significant future production were also studied. A brief appraisal of the base-metal deposits was made, and deposits of iron ore in Honduras and of lead and zinc ores in Guatemala were mapped. In addition, studies were made of the regional geology of some areas, data were collected from many sources, and a new map of the geology of Central America was compiled.

  12. 14 CFR 13.125 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 14 Aeronautics and Space 1 2011-01-01 2011-01-01 false Depositions. 13.125 Section 13.125....125 Depositions. Depositions for investigative purposes may be taken at the discretion of the Presiding Officer with reasonable notice to the party under investigation. Such depositions shall be taken...

  13. 14 CFR 13.125 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 14 Aeronautics and Space 1 2010-01-01 2010-01-01 false Depositions. 13.125 Section 13.125....125 Depositions. Depositions for investigative purposes may be taken at the discretion of the Presiding Officer with reasonable notice to the party under investigation. Such depositions shall be taken...

  14. 46 CFR 502.287 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 9 2011-10-01 2011-10-01 false Depositions. 502.287 Section 502.287 Shipping FEDERAL... Investigations § 502.287 Depositions. The Commission, or its duly authorized representative, may order testimony to be taken by deposition in any investigation at any stage of such investigation. Such depositions...

  15. 7 CFR 47.16 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 2 2010-01-01 2010-01-01 false Depositions. 47.16 Section 47.16 Agriculture... Depositions. (a) Application for taking deposition. Upon the application of a party to the proceeding, the... of testimony by deposition. The application shall be in writing, shall be filed with the Hearing...

  16. 16 CFR 2.10 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 16 Commercial Practices 1 2010-01-01 2010-01-01 false Depositions. 2.10 Section 2.10 Commercial... Inquiries; Investigations; Compulsory Processes § 2.10 Depositions. In investigations other than those... taken by deposition at any stage of such investigation. Such depositions may be taken before any person...

  17. 46 CFR 502.287 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 9 2010-10-01 2010-10-01 false Depositions. 502.287 Section 502.287 Shipping FEDERAL... Investigations § 502.287 Depositions. The Commission, or its duly authorized representative, may order testimony to be taken by deposition in any investigation at any stage of such investigation. Such depositions...

  18. 22 CFR 18.17 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 22 Foreign Relations 1 2010-04-01 2010-04-01 false Depositions. 18.17 Section 18.17 Foreign... Administrative Enforcement Proceedings § 18.17 Depositions. Depositions for use at a hearing may, with the... Director General or the respondent or their duly authorized representatives. Depositions may be taken upon...

  19. 22 CFR 18.17 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 22 Foreign Relations 1 2011-04-01 2011-04-01 false Depositions. 18.17 Section 18.17 Foreign... Administrative Enforcement Proceedings § 18.17 Depositions. Depositions for use at a hearing may, with the... Director General or the respondent or their duly authorized representatives. Depositions may be taken upon...

  20. 7 CFR 47.16 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 7 Agriculture 2 2011-01-01 2011-01-01 false Depositions. 47.16 Section 47.16 Agriculture... Depositions. (a) Application for taking deposition. Upon the application of a party to the proceeding, the... of testimony by deposition. The application shall be in writing, shall be filed with the Hearing...

  1. 16 CFR 2.10 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 16 Commercial Practices 1 2011-01-01 2011-01-01 false Depositions. 2.10 Section 2.10 Commercial... Inquiries; Investigations; Compulsory Processes § 2.10 Depositions. In investigations other than those... taken by deposition at any stage of such investigation. Such depositions may be taken before any person...

  2. Reactive polymer fused deposition manufacturing

    DOEpatents

    Kunc, Vlastimil; Rios, Orlando; Love, Lonnie J.; Duty, Chad E.; Johs, Alexander

    2017-05-16

    Methods and compositions for additive manufacturing that include reactive or thermosetting polymers, such as urethanes and epoxies. The polymers are melted, partially cross-linked prior to the depositing, deposited to form a component object, solidified, and fully cross-linked. These polymers form networks of chemical bonds that span the deposited layers. Application of a directional electromagnetic field can be applied to aromatic polymers after deposition to align the polymers for improved bonding between the deposited layers.

  3. 31 CFR 8.65 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 31 Money and Finance: Treasury 1 2010-07-01 2010-07-01 false Depositions. 8.65 Section 8.65 Money..., TOBACCO AND FIREARMS Disciplinary Proceedings § 8.65 Depositions. Depositions for use at a hearing may... or the respondent or their authorized representatives. Depositions may be taken upon oral or written...

  4. 7 CFR 900.61 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Depositions. 900.61 Section 900.61 Agriculture... Governing Proceedings on Petitions To Modify or To Be Exempted From Marketing Orders § 900.61 Depositions. (a) Procedure in lieu of deposition. Before any party may have testimony taken by deposition, said...

  5. 29 CFR 2200.56 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 9 2010-07-01 2010-07-01 false Depositions. 2200.56 Section 2200.56 Labor Regulations... Prehearing Procedures and Discovery § 2200.56 Depositions. (a) General. Depositions of parties, intervenors... Judge following the filing of a motion of a party stating good and just reasons. All depositions shall...

  6. 29 CFR 2200.56 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 9 2011-07-01 2011-07-01 false Depositions. 2200.56 Section 2200.56 Labor Regulations... Prehearing Procedures and Discovery § 2200.56 Depositions. (a) General. Depositions of parties, intervenors... Judge following the filing of a motion of a party stating good and just reasons. All depositions shall...

  7. 7 CFR 900.61 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 7 Agriculture 8 2011-01-01 2011-01-01 false Depositions. 900.61 Section 900.61 Agriculture... Governing Proceedings on Petitions To Modify or To Be Exempted From Marketing Orders § 900.61 Depositions. (a) Procedure in lieu of deposition. Before any party may have testimony taken by deposition, said...

  8. 31 CFR 8.65 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 31 Money and Finance: Treasury 1 2011-07-01 2011-07-01 false Depositions. 8.65 Section 8.65 Money..., TOBACCO AND FIREARMS Disciplinary Proceedings § 8.65 Depositions. Depositions for use at a hearing may... or the respondent or their authorized representatives. Depositions may be taken upon oral or written...

  9. Becquerel Crater Deposit

    NASA Technical Reports Server (NTRS)

    2002-01-01

    (Released 28 May 2002) The finely layered deposit in Becquerel crater, seen in the center of this THEMIS image, is slowly being eroded away by the action of windblown sand. Dark sand from a source north of the bright deposit is collecting along its northern edge, forming impressive barchan style dunes. These vaguely boomerang-shaped dunes form with their two points extending in the downwind direction, demonstrating that the winds capable of moving sand grains come from the north. Grains that leave the dunes climb the eroding stair-stepped layers, collecting along the cliff faces before reaching the crest of the deposit. Once there, the sand grains are unimpeded and continue down the south side of the deposit without any significant accumulation until they fall off the steep cliffs of the southern margin. The boat-hull shaped mounds and ridges of bright material called yardangs form in response to the scouring action of the migrating sand. To the west, the deposit has thinned enough that the barchan dunes extend well into the deeply eroded north-south trending canyons. Sand that reaches the south side collects and reforms barchan dunes with the same orientation as those on the north side of the deposit. Note the abrupt transition between the bright material and the dark crater floor on the southern margin. Steep cliffs are present with no indication of rubble from the obvious erosion that produced them. The lack of debris at the base of the cliffs is evidence that the bright material is readily broken up into particles that can be transported away by the wind. The geological processes that are destroying the Becquerel crater deposit appear active today. But it is also possible that they are dormant, awaiting a particular set of climatic conditions that produces the right winds and perhaps even temperatures to allow the erosion to continue.

  10. Precambrian Sulphide Deposits

    NASA Astrophysics Data System (ADS)

    Doe, Bruce R.

    1984-04-01

    This book is dedicated to Howard S. Robinson, who was born and educated in the United States, but who spent his professional career in Canada with McIntyre Porcupine Mines, concentrating on Precambrian mineral deposits. Although his career in mineral exploration was distinguished, his major contribution to earth science was probably as one of the founders of the Geological Association of Canada, an institution to which he made a bequest in his will. With this background, the strong emphasis on Canadian Precambrian mineral deposits should come as no surprise; of the 23 papers in this book, 21 are solely or primarily devoted to Canadian deposits. The two exceptions—those describing the Balmat, N.Y., zinc mines (at times the largest zinc producer in the United States) and the Crandon, Wisconsin, volcanogenic zinc-copper massive-sulfide deposit (the largest deposit of its kind found in the 1970s)—are each within a couple of hundred kilometers of the Canadian border. Although the title of the book is more expansive than the actual topics discussed, Canada is rich in Precambrian rocks and ore bodies, and Canadian scientists have been especially alert to tectonic influences in the formation of mineral deposits. These features, plus the fact that the country contains a very well exposed expanse of Archean rocks which is the largest in the world, facilitate the study of early crustal evolution and make the book of particular interest to geophysicists.

  11. ESTIMATES OF CLOUD WATER DEPOSITION AT MOUNTAIN DEPOSITION AT MOUNTAIN ACID DEPOSITION PROGRAM SITES IN THE APPALACHIAN MOUNTAINS

    EPA Science Inventory

    Cloud water deposition was estimated at three high elevation sites in the Appalachian Mountains of the eastern United States (Whiteface Mountain, NY, Whitetop Mountain, VA, and Clingrnan's Dome, TN) from 1994 through 1999 as part of the Mountain Acid Deposition Program (MADPro). ...

  12. Quartz-pebble-conglomerate gold deposits: Chapter P in Mineral deposit models for resource assessment

    USGS Publications Warehouse

    Taylor, Ryan D.; Anderson, Eric D.

    2018-05-17

    Quartz-pebble-conglomerate gold deposits represent the largest repository of gold on Earth, largely due to the deposits of the Witwatersrand Basin, which account for nearly 40 percent of the total gold produced throughout Earth’s history. This deposit type has had a controversial history in regards to genetic models. However, most researchers conclude that they are paleoplacer deposits that have been modified by metamorphism and hydrothermal fluid flow subsequent to initial sedimentation.The deposits are found exclusively within fault-bounded depositional basins. The periphery of these basins commonly consists of granite-greenstone terranes, classic hosts for lode gold that source the detrital material infilling the basin. The gold reefs are typically located along unconformities or, less commonly, at the top of sedimentary beds. Large quartz pebbles and heavy-mineral concentrates are found associated with the gold. Deposits that formed prior to the Great Oxidation Event (circa 2.4 giga-annum [Ga]) contain pyrite, whereas younger deposits contain iron oxides. Uranium minerals and hydrocarbons are also notable features of some deposits.Much of the gold in these types of deposits forms crystalline features that are the product of local remobilization. However, some gold grains preserve textures that are undoubtedly of detrital origin. Other heavy minerals, such as pyrite, contain growth banding that is truncated along broken margins, which indicates that they were transported into place as opposed to forming by in situ growth in a hydrothermal setting.The ore tailings associated with these deposits commonly contain uranium-rich minerals and sulfides. Oxidation of the sulfides releases sulfuric acid and mobilizes various metals into the environment. The neutralizing potential of the tailings is minimal, since carbonate minerals are rare. The continuity of the tabular ore bodies, such as those of the Witwatersrand Basin, has allowed these mines to be the deepest in

  13. Ni-Co laterite deposits

    USGS Publications Warehouse

    Marsh, Erin E.; Anderson, Eric D.

    2011-01-01

    Nickel-cobalt (Ni-Co) laterite deposits are an important source of nickel (Ni). Currently, there is a decline in magmatic Ni-bearing sulfide lode deposit resources. New efforts to develop an alternative source of Ni, particularly with improved metallurgy processes, make the Ni-Co laterites an important exploration target in anticipation of the future demand for Ni. This deposit model provides a general description of the geology and mineralogy of Ni-Co laterite deposits, and contains discussion of the influences of climate, geomorphology (relief), drainage, tectonism, structure, and protolith on the development of favorable weathering profiles. This model of Ni-Co laterite deposits represents part of the U.S. Geological Survey Mineral Resources Program's effort to update the existing models to be used for an upcoming national mineral resource assessment.

  14. 25 CFR 571.11 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 25 Indians 2 2010-04-01 2010-04-01 false Depositions. 571.11 Section 571.11 Indians NATIONAL... INVESTIGATIONS Subpoenas and Depositions § 571.11 Depositions. (a) Any party wishing to depose a witness shall... shown. A Commissioner or a presiding official may order testimony to be taken by deposition in any...

  15. 19 CFR 210.28 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 19 Customs Duties 3 2010-04-01 2010-04-01 false Depositions. 210.28 Section 210.28 Customs Duties... ADJUDICATION AND ENFORCEMENT Discovery and Compulsory Process § 210.28 Depositions. (a) When depositions may be... investigation, any party may take the testimony of any person, including a party, by deposition upon oral...

  16. 30 CFR 44.25 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 30 Mineral Resources 1 2011-07-01 2011-07-01 false Depositions. 44.25 Section 44.25 Mineral... Depositions. (a) Purpose. For reasons of unavailability or for purpose of discovery, the testimony of any witness may be taken by deposition. (b) Form. Depositions may be taken before any person having the power...

  17. 45 CFR 501.5 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 45 Public Welfare 3 2011-10-01 2011-10-01 false Depositions. 501.5 Section 501.5 Public Welfare..., DEPARTMENT OF JUSTICE RULES OF PRACTICE SUBPOENAS, DEPOSITIONS, AND OATHS § 501.5 Depositions. (a) Application to take. (1) An application to take a deposition must be in writing setting forth the reason why...

  18. 39 CFR 955.17 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 39 Postal Service 1 2011-07-01 2011-07-01 false Depositions. 955.17 Section 955.17 Postal Service... APPEALS § 955.17 Depositions. (a) When depositions permitted. After an appeal has been docketed and... for good cause shown, order the taking of testimony of any person by deposition upon oral examination...

  19. 15 CFR 904.241 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 15 Commerce and Foreign Trade 3 2010-01-01 2010-01-01 false Depositions. 904.241 Section 904.241... and Appeal Procedures Discovery § 904.241 Depositions. (a) Notice. If a motion for deposition is granted, and unless otherwise ordered by the Judge, the party taking the deposition of any person must...

  20. 45 CFR 501.5 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 45 Public Welfare 3 2010-10-01 2010-10-01 false Depositions. 501.5 Section 501.5 Public Welfare..., DEPARTMENT OF JUSTICE RULES OF PRACTICE SUBPOENAS, DEPOSITIONS, AND OATHS § 501.5 Depositions. (a) Application to take. (1) An application to take a deposition must be in writing setting forth the reason why...

  1. 30 CFR 44.25 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 1 2010-07-01 2010-07-01 false Depositions. 44.25 Section 44.25 Mineral... Depositions. (a) Purpose. For reasons of unavailability or for purpose of discovery, the testimony of any witness may be taken by deposition. (b) Form. Depositions may be taken before any person having the power...

  2. 15 CFR 904.241 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 15 Commerce and Foreign Trade 3 2011-01-01 2011-01-01 false Depositions. 904.241 Section 904.241... and Appeal Procedures Discovery § 904.241 Depositions. (a) Notice. If a motion for deposition is granted, and unless otherwise ordered by the Judge, the party taking the deposition of any person must...

  3. 16 CFR 1605.7 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 16 Commercial Practices 2 2011-01-01 2011-01-01 false Depositions. 1605.7 Section 1605.7... Inquiries § 1605.7 Depositions. (a) The Commission may order and, by subpoena, may compel testimony to be taken by deposition at any stage of any investigation. Such depositions may be taken before any person...

  4. 20 CFR 901.46 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 20 Employees' Benefits 3 2011-04-01 2011-04-01 false Depositions. 901.46 Section 901.46 Employees... § 901.46 Depositions. Depositions for use at a hearing may, with the written approval of the... representatives. Depositions may be taken upon oral or written interrogatories, upon not less than 10 days written...

  5. 19 CFR 210.28 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 19 Customs Duties 3 2011-04-01 2011-04-01 false Depositions. 210.28 Section 210.28 Customs Duties... ADJUDICATION AND ENFORCEMENT Discovery and Compulsory Process § 210.28 Depositions. (a) When depositions may be... investigation, any party may take the testimony of any person, including a party, by deposition upon oral...

  6. 16 CFR 1118.6 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 16 Commercial Practices 2 2011-01-01 2011-01-01 false Depositions. 1118.6 Section 1118.6..., Inspections, and Inquiries § 1118.6 Depositions. (a) The Commission by subpoena may require testimony to be taken by deposition at any stage of any investigation. Depositions may be taken before any person who is...

  7. 39 CFR 955.17 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 39 Postal Service 1 2010-07-01 2010-07-01 false Depositions. 955.17 Section 955.17 Postal Service... APPEALS § 955.17 Depositions. (a) When depositions permitted. After an appeal has been docketed and... for good cause shown, order the taking of testimony of any person by deposition upon oral examination...

  8. 16 CFR 1118.6 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 16 Commercial Practices 2 2010-01-01 2010-01-01 false Depositions. 1118.6 Section 1118.6..., Inspections, and Inquiries § 1118.6 Depositions. (a) The Commission by subpoena may require testimony to be taken by deposition at any stage of any investigation. Depositions may be taken before any person who is...

  9. 27 CFR 71.125 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 2 2010-04-01 2010-04-01 false Depositions. 71.125... Miscellaneous § 71.125 Depositions. The administrative law judge may take or order the taking of depositions by... testimony shall be reduced to writing by the person taking the deposition, or under his direction, and the...

  10. 20 CFR 901.46 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 20 Employees' Benefits 3 2010-04-01 2010-04-01 false Depositions. 901.46 Section 901.46 Employees... § 901.46 Depositions. Depositions for use at a hearing may, with the written approval of the... representatives. Depositions may be taken upon oral or written interrogatories, upon not less than 10 days written...

  11. 25 CFR 571.11 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 25 Indians 2 2011-04-01 2011-04-01 false Depositions. 571.11 Section 571.11 Indians NATIONAL... INVESTIGATIONS Subpoenas and Depositions § 571.11 Depositions. (a) Any party wishing to depose a witness shall... shown. A Commissioner or a presiding official may order testimony to be taken by deposition in any...

  12. 27 CFR 71.125 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 2 2011-04-01 2011-04-01 false Depositions. 71.125... Miscellaneous § 71.125 Depositions. The administrative law judge may take or order the taking of depositions by... testimony shall be reduced to writing by the person taking the deposition, or under his direction, and the...

  13. 16 CFR 1605.7 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 16 Commercial Practices 2 2010-01-01 2010-01-01 false Depositions. 1605.7 Section 1605.7... Inquiries § 1605.7 Depositions. (a) The Commission may order and, by subpoena, may compel testimony to be taken by deposition at any stage of any investigation. Such depositions may be taken before any person...

  14. 39 CFR 3001.33 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 39 Postal Service 1 2011-07-01 2011-07-01 false Depositions. 3001.33 Section 3001.33 Postal... Applicability § 3001.33 Depositions. (a) When permissible. The testimony of a witness may be taken by deposition... the hearing is closed. An authorization to take the deposition of a witness will be issued only if (1...

  15. 33 CFR 20.605 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 33 Navigation and Navigable Waters 1 2010-07-01 2010-07-01 false Depositions. 20.605 Section 20....605 Depositions. (a) The ALJ may order a deposition only upon a showing of good cause and upon a... preserved for presentation at the hearing. (b) Testimony may be taken by deposition upon approval of the ALJ...

  16. 33 CFR 20.605 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 33 Navigation and Navigable Waters 1 2011-07-01 2011-07-01 false Depositions. 20.605 Section 20....605 Depositions. (a) The ALJ may order a deposition only upon a showing of good cause and upon a... preserved for presentation at the hearing. (b) Testimony may be taken by deposition upon approval of the ALJ...

  17. 39 CFR 3001.33 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 39 Postal Service 1 2010-07-01 2010-07-01 false Depositions. 3001.33 Section 3001.33 Postal... Applicability § 3001.33 Depositions. (a) When permissible. The testimony of a witness may be taken by deposition... the hearing is closed. An authorization to take the deposition of a witness will be issued only if (1...

  18. Probabilistic estimates of number of undiscovered deposits and their total tonnages in permissive tracts using deposit densities

    USGS Publications Warehouse

    Singer, Donald A.; Kouda, Ryoichi

    2011-01-01

    Empirical evidence indicates that processes affecting number and quantity of resources in geologic settings are very general across deposit types. Sizes of permissive tracts that geologically could contain the deposits are excellent predictors of numbers of deposits. In addition, total ore tonnage of mineral deposits of a particular type in a tract is proportional to the type’s median tonnage in a tract. Regressions using size of permissive tracts and median tonnage allow estimation of number of deposits and of total tonnage of mineralization. These powerful estimators, based on 10 different deposit types from 109 permissive worldwide control tracts, generalize across deposit types. Estimates of number of deposits and of total tonnage of mineral deposits are made by regressing permissive area, and mean (in logs) tons in deposits of the type, against number of deposits and total tonnage of deposits in the tract for the 50th percentile estimates. The regression equations (R2 = 0.91 and 0.95) can be used for all deposit types just by inserting logarithmic values of permissive area in square kilometers, and mean tons in deposits in millions of metric tons. The regression equations provide estimates at the 50th percentile, and other equations are provided for 90% confidence limits for lower estimates and 10% confidence limits for upper estimates of number of deposits and total tonnage. Equations for these percentile estimates along with expected value estimates are presented here along with comparisons with independent expert estimates. Also provided are the equations for correcting for the known well-explored deposits in a tract. These deposit-density models require internally consistent grade and tonnage models and delineations for arriving at unbiased estimates.

  19. Variable temperature semiconductor film deposition

    DOEpatents

    Li, X.; Sheldon, P.

    1998-01-27

    A method of depositing a semiconductor material on a substrate is disclosed. The method sequentially comprises (a) providing the semiconductor material in a depositable state such as a vapor for deposition on the substrate; (b) depositing the semiconductor material on the substrate while heating the substrate to a first temperature sufficient to cause the semiconductor material to form a first film layer having a first grain size; (c) continually depositing the semiconductor material on the substrate while cooling the substrate to a second temperature sufficient to cause the semiconductor material to form a second film layer deposited on the first film layer and having a second grain size smaller than the first grain size; and (d) raising the substrate temperature, while either continuing or not continuing to deposit semiconductor material to form a third film layer, to thereby anneal the film layers into a single layer having favorable efficiency characteristics in photovoltaic applications. A preferred semiconductor material is cadmium telluride deposited on a glass/tin oxide substrate already having thereon a film layer of cadmium sulfide.

  20. Variable temperature semiconductor film deposition

    DOEpatents

    Li, Xiaonan; Sheldon, Peter

    1998-01-01

    A method of depositing a semiconductor material on a substrate. The method sequentially comprises (a) providing the semiconductor material in a depositable state such as a vapor for deposition on the substrate; (b) depositing the semiconductor material on the substrate while heating the substrate to a first temperature sufficient to cause the semiconductor material to form a first film layer having a first grain size; (c) continually depositing the semiconductor material on the substrate while cooling the substrate to a second temperature sufficient to cause the semiconductor material to form a second film layer deposited on the first film layer and having a second grain size smaller than the first grain size; and (d) raising the substrate temperature, while either continuing or not continuing to deposit semiconductor material to form a third film layer, to thereby anneal the film layers into a single layer having favorable efficiency characteristics in photovoltaic applications. A preferred semiconductor material is cadmium telluride deposited on a glass/tin oxide substrate already having thereon a film layer of cadmium sulfide.

  1. Post-depositional fracturing and subsidence of pumice flow deposits: Lascar Volcano, Chile.

    PubMed

    Whelley, Patrick L; Jay, J; Calder, E S; Pritchard, M E; Cassidy, N J; Alcaraz, S; Pavez, A

    Unconsolidated pyroclastic flow deposits of the 1993 eruption of Lascar Volcano, Chile, have, with time, become increasingly dissected by a network of deeply penetrating fractures. The fracture network comprises orthogonal sets of decimeter-wide linear voids that form a pseudo-polygonal grid visible on the deposit surface. In this work, we combine shallow surface geophysical imaging tools with remote sensing observations and direct field measurements of the deposit to investigate these fractures and their underlying causal mechanisms. Based on ground penetrating radar images, the fractures are observed to have propagated to depths of up to 10 m. In addition, orbiting radar interferometry shows that deposit subsidence of up to 1 cm/year -1 occurred between 1993 and 1996 with continued subsidence occurring at a slower rate thereafter. In situ measurements show that 1 m below the surface, the 1993 deposits remain 5°C to 15°C hotter, 18 years after emplacement, than adjacent deposits. Based on the observed subsidence as well as estimated cooling rates, the fractures are inferred to be the combined result of deaeration, thermal contraction, and sedimentary compaction in the months to years following deposition. Significant environmental factors, including regional earthquakes in 1995 and 2007, accelerated settling at punctuated moments in time. The spatially variable fracture pattern relates to surface slope and lithofacies variations as well as substrate lithology. Similar fractures have been reported in other ignimbrites but are generally exposed only in cross section and are often attributed to formation by external forces. Here we suggest that such interpretations should be invoked with caution, and deformation including post-emplacement subsidence and fracturing of loosely packed ash-rich deposits in the months to years post-emplacement is a process inherent in the settling of pyroclastic material.

  2. On the mineral characteristics and geochemistry of the Florida phosphate of Four Corners and Hardee County mines

    NASA Astrophysics Data System (ADS)

    Baghdady, Ashraf R.; Howari, Fares M.; Al-Wakeel, Mohamed I.

    2016-08-01

    The Florida phosphate deposits in Four Corners and Hardee County mines are composed mainly of phosphate minerals and quartz in addition to subordinate proportions of feldspars, dolomite, calcite, gypsum, kaolinite, attapulgite and montmorillonite. These phosphorites contain three structurally different types of mudclasts: massive mudclasts, mudclasts with concentric structure and mudclasts consisting of agglomerates of apatite microparticles. The latter are represented by particles resembling phosphatized fossil bacteria associated with microbial filaments, and hollow apatite particles having surfacial coatings and connected to microbial filaments. The Florida phosphate particles are reworked and vary in mineral composition, color and shape. They are composed of a mixture of well-crystalline species including carbonate fluorapatite (francolite), carbonate apatite and fluorapatite. The color variation of the phosphate particles is related to difference in mineral composition, extent of diagenetic effects and reworking. The light-colored mudclasts are characterized by the presence of carbonate apatite and aluminum hydroxide phosphate minerals, whereas the dark mudclasts are rich in iron aluminum hydroxide phosphate minerals. The Florida phosphorites are suggested to be formed partially by authigenetic precipitation, replacement of the sea floor carbonate and diatomite, and microbial processes. With respect to elemental geochemistry, the analyzed particles contain small percentages of sulfur and iron which are related to the occurrence of pyrite. Traces of silica and alumina are recorded which may be attributed to the diagenetic. Some of the tested particles are relatively rich in phosphorous, fluorine, calcium, and magnesium, while poor in silicon, potassium and sulfur. Whereas, the bioclasts (especially teeth) are relatively rich in calcium, phosphorous and fluorine while poor in silicon, aluminum, magnesium and potassium. Hence, the microchemical analyses revealed

  3. 29 CFR 18.22 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 1 2011-07-01 2011-07-01 false Depositions. 18.22 Section 18.22 Labor Office of the... ADMINISTRATIVE LAW JUDGES General § 18.22 Depositions. (a) When, how, and by whom taken. The deposition of any witness may be taken at any stage of the proceeding at reasonable times. Depositions may be taken by oral...

  4. 29 CFR 18.22 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 1 2010-07-01 2010-07-01 true Depositions. 18.22 Section 18.22 Labor Office of the... ADMINISTRATIVE LAW JUDGES General § 18.22 Depositions. (a) When, how, and by whom taken. The deposition of any witness may be taken at any stage of the proceeding at reasonable times. Depositions may be taken by oral...

  5. Low-fluorine Stockwork Molybdenite Deposits

    USGS Publications Warehouse

    Ludington, Steve; Hammarstrom, Jane; Piatak, Nadine M.

    2009-01-01

    Low-fluorine stockwork molybdenite deposits are closely related to porphyry copper deposits, being similar in their tectonic setting (continental volcanic arc) and the petrology (calc-alkaline) of associated igneous rock types. They are mainly restricted to the Cordillera of western Canada and the northwest United States, and their distribution elsewhere in the world may be limited. The deposits consist of stockwork bodies of molybdenite-bearing quartz veinlets that are present in and around the upper parts of intermediate to felsic intrusions. The deposits are relatively low grade (0.05 to 0.2 percent Mo), but relatively large, commonly >50 million tons. The source plutons for these deposits range from granodiorite to granite in composition; the deposits primarily form in continental margin subduction-related magmatic arcs, often concurrent with formation of nearby porphyry copper deposits. Oxidation of pyrite in unmined deposits or in tailings and waste rock during weathering can lead to development of acid-rock drainage and limonite-rich gossans. Waters associated with low-fluorine stockwork molybdenite deposits tend to be nearly neutral in pH; variable in concentrations of molybdenum (10,000 ug/L); below regulatory guidelines for copper, iron, lead, zinc, and mercury; and locally may exceed guidelines for arsenic, cadmium, and selenium.

  6. Deposition, Chapter 3

    Treesearch

    K.C. Weathers; J.A. Lynch

    2011-01-01

    To determine the effects of air pollution on ecological systems using the critical load approach, accurate estimates of total nitrogen (N) deposition are essential. Empirical critical loads are set by relating observed ecosystem responses to N deposition (measured, experimentally manipulated, or modeled).

  7. Developing Depositional Models for Mercury Contaminated Floodplain Deposits Using Geomorphic Mapping and GIS in South River, Virginia

    NASA Astrophysics Data System (ADS)

    Barbieri, A.; Pizzuto, J.; O'Neal, M. A.; Rhoades, E.

    2007-12-01

    Mercury was introduced into the South River from the 1930s to the 1950s from an industrial plant in Waynesboro, Virginia. Mercury contamination in fish tissue continues to exceed acceptable levels. The contaminated sediments in the river's floodplains are probably the present source of mercury to the South River ecosystem. Locating and determining the extent and depositional history of these deposits are important for understanding the mercury cycle in the river as well as for remediation plans. The South River is a sinuous, single thread alluvial river with frequent bedrock exposures along its bed and banks. Overbank deposits are discontinuous and thin. Rates of lateral migration by the South River are extremely low, averaging 0.02 m/yr, and the river has been influenced by mill dams along a 19 km study reach. This 19 km section of the 37 km river reach was selected for the study because of its high concentration of Hg. Six different categories of floodplain deposits dating from 1937-2005 have been identified throughout the river using studies of historical aerial photographs in a GIS framework, field mapping, dendro- and radionuclide dating, grain size and Hg analysis. Not surprisingly, traditional depositional models of meandering rivers do not apply. Floodplain depositional units include mill dam deposits, point bar/bench deposits, concave bank bench deposits, islands, cattle deposits, and tributary confluences deposits. The most important deposits for sequestering historic mercury are those that also store the most silt and clay. These include mill dam deposits, point bar/bench deposits, concave bank deposits, and tributary confluence deposits. Many of these deposits represent reservoirs of mercury-contaminated sediments that could supply significant amounts of mercury into the river presently and in the future.

  8. Early Proterozoic (2.04 GA) Phoshorites of Pechenga Greenstone Belt and Their Origin

    NASA Technical Reports Server (NTRS)

    Rozanov, Alexei Yu.; Astafieva, Marina M.; Hoover, Richard B.

    2007-01-01

    No principal differences have been found between microfossils described from Cambrian and Phanerozoic and the 2000 Ma phosphorites. Numerous samples revealed diverse microbial microstructures interpreted as cyanobacterial mats consisting of filamentous (1-3 microns in diameter, 20 microns in length), coccoidal (0.8-1.0 microns) and ellipsoidal or rod-shaped microfossils (0.8 microns in diameter, around 2 microns in length) which morphologically resemble modern Microcoleus and Siphonophycus, Thiocapsa, and Rhabdoderma, respectively, reported from alkali ne or saline environment_ The sequence of the early Palaeoproterozoic events which point to a significant oxidation of the hydrosphere, including the formation of phosphorites and changes in the phosphorous cycle, mimics the sequence which was repeated at the Neoproterozoic-Cembrian transition, implying that oxidation of the terrestrial atmosphere-hydrosphere system experienced an irregular cyclic development.

  9. A deposit model for carbonatite and peralkaline intrusion-related rare earth element deposits: Chapter J in Mineral deposit models for resource assessment

    USGS Publications Warehouse

    Verplanck, Philip L.; Van Gosen, Bradley S.; Seal, Robert R.; McCafferty, Anne E.

    2014-01-01

    The greatest environmental challenges associated with carbonatite and peralkaline intrusion-related rare earth element deposits center on the associated uranium and thorium. Considerable uncertainty exists around the toxicity of rare earth elements and warrants further investigation. The acid-generating potential of carbonatites and peralkaline intrusion-related deposits is low due to the dominance of carbonate minerals in carbonatite deposits, the presence of feldspars and minor calcite within the alkaline intrusion deposits, and only minor quantities of potentially acid-generating sulfides. Therefore, acid-drainage issues are not likely to be a major concern associated with these deposits. Uranium has the potential to be recovered as a byproduct, which would mitigate some of its environmental effects. However, thorium will likely remain a waste-stream product that will require management since progress is not being made towards the development of thorium-based nuclear reactors in the United States or other large scale commercial uses. Because some deposits are rich in fluorine and beryllium, these elements may be of environmental concern in certain locations.

  10. Deposits of the Peruvian Pisco Formation compared to layered deposits on Mars

    NASA Astrophysics Data System (ADS)

    Sowe, M.; Bishop, J. L.; Gross, C.; Walter, S.

    2013-09-01

    Deposits of the Peruvian Pisco Formation are morphologically similar to the mounds of Juventae Chasma at the equatorial region on Mars (Fig. 1). By analyzing these deposits, we hope to gain information about the environmental conditions that prevailed during sediment deposition and erosion, hence conditions that might be applicable to the Martian layered and hydrated deposits. Mariner 9 data of the Martian mid-latitudes have already shown evidence of the wind-sculptured landforms that display the powerful prevailing eolian regime [1]. In addition, [2] reported on similarities between Martian erosional landforms and those of the rainless coastal desert of central Peru from the Paracas peninsula to the Rio Ica. As indicated by similar erosional patterns, hyper-arid conditions and unidirectional winds must have dominated at least after deposition of the sediments, which are intermixed volcaniclastic materials and evaporate minerals at both locations. Likewise, variations in composition are displayed by alternating layers of different competence. The Pisco formation bears yardangs on siltstones, sandstones and clays with volcaniclastic admixtures [3] whereas the presence of sulphate minerals and the omnipresent mafic mineralogy has been reported for the layered mounds of Juventae Chasma equally [4]. Likewise, a volcanic airfall deposition and lacustrine formation have been proposed for the sulphate-rich deposits of Juventae Chasma [5,6]. In order to find out about potential spectral similarities, we performed a detailed spectral analysis of the surface by using LANDSAT and Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) VNIR/ SWIR data (visible to near-infrared and shortwave infrared region).

  11. Porphyry deposits of the Canadian Cordillera

    USGS Publications Warehouse

    McMillan, W.J.; Thompson, J.F.H.; Hart, C.J.R.; Johnston, S.T.

    1996-01-01

    Porphyry deposits are intrusion-related, large tonnage low grade mineral deposits with metal assemblages that may include all or some of copper, molybdenum, gold and silver. The genesis of these deposits is related to the emplacement of intermediate to felsic, hypabyssal, generally porphyritic intrusions that are commonly formed at convergent plate margins. Porphyry deposits of the Canadian Cordillera occur in association with two distinctive intrusive suites: calc-alkalic and alkalic. In the Canadian Cordillera, these deposits formed during two separate time periods: Late Triassic to Middle Jurassic (early Mesozoic), and Late Cretaceous to Eocene (Mesozoic-Cenozoic). Deposits of the early Mesozoic period occur in at least three different arc terranes (Wrangellia, Stikinia and Quesnellia) with a single deposit occurring in the oceanic assemblage of the Cache Creek terrane. These terranes were located outboard from continental North America during formation of most of their contained early Mesozoic porphyry deposits. Some of the deposits of this early period may have been emplaced during terrane collisions. Metal assemblages in deposits of the calc-alkalic suite include Mo-Cu (Brenda), Cu-Mo (Highland Valley, Gibraltar), Cu-Mo-Au-Ag (Island Copper, Schaft Creek) and Cu-Au (Kemess, Kerr).The alkalic suite deposits are characterized by a Cu-Au assemblage (Copper Mountain, Afton-Ajax, Mt. Milligan, Mount Polley, Galore Creek). Although silver is recovered from calc-alkalic and alkalic porphyry copper mining operations, silver data are seldom included in the published reserve figures. Those available are in the range of 1-2 grams per tonne (g??t-1). Alkalic suite deposits are restricted to the early Mesozoic and display distinctive petrology, alteration and mineralization that suggest a similar tectonic setting for both Quesnellia and Stikinia in Early Jurassic time. The younger deposits, late Mesozoic to Cenozoic in age, formed in an intracontinental setting, after the

  12. Statistical guides to estimating the number of undiscovered mineral deposits: an example with porphyry copper deposits

    USGS Publications Warehouse

    Singer, Donald A.; Menzie, W.D.; Cheng, Qiuming; Bonham-Carter, G. F.

    2005-01-01

    Estimating numbers of undiscovered mineral deposits is a fundamental part of assessing mineral resources. Some statistical tools can act as guides to low variance, unbiased estimates of the number of deposits. The primary guide is that the estimates must be consistent with the grade and tonnage models. Another statistical guide is the deposit density (i.e., the number of deposits per unit area of permissive rock in well-explored control areas). Preliminary estimates and confidence limits of the number of undiscovered deposits in a tract of given area may be calculated using linear regression and refined using frequency distributions with appropriate parameters. A Poisson distribution leads to estimates having lower relative variances than the regression estimates and implies a random distribution of deposits. Coefficients of variation are used to compare uncertainties of negative binomial, Poisson, or MARK3 empirical distributions that have the same expected number of deposits as the deposit density. Statistical guides presented here allow simple yet robust estimation of the number of undiscovered deposits in permissive terranes. 

  13. Breakthrough to Non-Vacuum Deposition of Single-Crystal, Ultra-Thin, Homogeneous Nanoparticle Layers: A Better Alternative to Chemical Bath Deposition and Atomic Layer Deposition

    PubMed Central

    Liao, Yu-Kuang; Liu, Yung-Tsung; Hsieh, Dan-Hua; Shen, Tien-Lin; Hsieh, Ming-Yang; Tzou, An-Jye; Chen, Shih-Chen; Tsai, Yu-Lin; Lin, Wei-Sheng; Chan, Sheng-Wen; Shen, Yen-Ping; Cheng, Shun-Jen; Chen, Chyong-Hua; Wu, Kaung-Hsiung; Chen, Hao-Ming; Kuo, Shou-Yi; Charlton, Martin D. B.; Hsieh, Tung-Po; Kuo, Hao-Chung

    2017-01-01

    Most thin-film techniques require a multiple vacuum process, and cannot produce high-coverage continuous thin films with the thickness of a few nanometers on rough surfaces. We present a new ”paradigm shift” non-vacuum process to deposit high-quality, ultra-thin, single-crystal layers of coalesced sulfide nanoparticles (NPs) with controllable thickness down to a few nanometers, based on thermal decomposition. This provides high-coverage, homogeneous thickness, and large-area deposition over a rough surface, with little material loss or liquid chemical waste, and deposition rates of 10 nm/min. This technique can potentially replace conventional thin-film deposition methods, such as atomic layer deposition (ALD) and chemical bath deposition (CBD) as used by the Cu(In,Ga)Se2 (CIGS) thin-film solar cell industry for decades. We demonstrate 32% improvement of CIGS thin-film solar cell efficiency in comparison to reference devices prepared by conventional CBD deposition method by depositing the ZnS NPs buffer layer using the new process. The new ZnS NPs layer allows reduction of an intrinsic ZnO layer, which can lead to severe shunt leakage in case of a CBD buffer layer. This leads to a 65% relative efficiency increase. PMID:28383488

  14. Dual Nitrate Isotopes in Dry Deposition: Utility for Partitioning Nox Source Contributions to Landscape Nitrogen Deposition

    EPA Science Inventory

    Dry deposition is a major component of total nitrogen deposition and thus an important source of bioavailable nitrogen to ecosystems. However, relative to wet deposition, less is known regarding the sources and spatial variability of dry deposition. This is in part due to diffi...

  15. 12 CFR 622.10 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... Formal Hearings § 622.10 Depositions. (a) Application to take deposition. Any party desiring to take the... or debate) shall be recorded by or under the direction of the person before whom the deposition is...

  16. 12 CFR 622.10 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... Formal Hearings § 622.10 Depositions. (a) Application to take deposition. Any party desiring to take the... or debate) shall be recorded by or under the direction of the person before whom the deposition is...

  17. Radionuclide deposition control

    DOEpatents

    Brehm, William F.; McGuire, Joseph C.

    1980-01-01

    The deposition of radionuclides manganese-54, cobalt-58 and cobalt-60 from liquid sodium coolant is controlled by providing surfaces of nickel or high nickel alloys to extract the radionuclides from the liquid sodium, and by providing surfaces of tungsten, molybdenum or tantalum to prevent or retard radionuclide deposition.

  18. The influences of target properties and deposition times on pulsed laser deposited hydroxyapatite films

    NASA Astrophysics Data System (ADS)

    Bao, Quanhe; Chen, Chuanzhong; Wang, Diangang; Liu, Junming

    2008-11-01

    Hydroxyapatite films were produced by pulsed laser deposition from three kinds of hydroxyapatite targets and with different deposition times. A JXA-8800R electron probe microanalyzer (EPMA) with a Link ISIS300 energy spectrum analyzer was used to give the secondary electron image (SE) and determine the element composition of the films. The phases of thin film were analyzed by a D/max-γc X-ray diffractometer (XRD). The Fourier-transform infrared spectroscopy (FT-IR) was used to characterize the hydroxyl, phosphate and other functional groups. The results show that deposited films were amorphous which mainly composed of droplet-like particles and vibration of PO 43- groups. With the target sintering temperature deposition times increasing, the density of droplets is decreased. While with deposition times increasing, the density of droplets is increased. With the target sintering temperature and deposition time increasing, the ratio of Ca/P is increasing and higher than that of theoretical value of HA.

  19. Advanced deposition model for thermal activated chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Cai, Dang

    Thermal Activated Chemical Vapor Deposition (TACVD) is defined as the formation of a stable solid product on a heated substrate surface from chemical reactions and/or dissociation of gaseous reactants in an activated environment. It has become an essential process for producing solid film, bulk material, coating, fibers, powders and monolithic components. Global market of CVD products has reached multi billions dollars for each year. In the recent years CVD process has been extensively used to manufacture semiconductors and other electronic components such as polysilicon, AlN and GaN. Extensive research effort has been directed to improve deposition quality and throughput. To obtain fast and high quality deposition, operational conditions such as temperature, pressure, fluid velocity and species concentration and geometry conditions such as source-substrate distance need to be well controlled in a CVD system. This thesis will focus on design of CVD processes through understanding the transport and reaction phenomena in the growth reactor. Since the in situ monitor is almost impossible for CVD reactor, many industrial resources have been expended to determine the optimum design by semi-empirical methods and trial-and-error procedures. This approach has allowed the achievement of improvements in the deposition sequence, but begins to show its limitations, as this method cannot always fulfill the more and more stringent specifications of the industry. To resolve this problem, numerical simulation is widely used in studying the growth techniques. The difficulty of numerical simulation of TACVD crystal growth process lies in the simulation of gas phase and surface reactions, especially the latter one, due to the fact that very limited kinetic information is available in the open literature. In this thesis, an advanced deposition model was developed to study the multi-component fluid flow, homogeneous gas phase reactions inside the reactor chamber, heterogeneous surface

  20. Stratiform chromite deposit model

    USGS Publications Warehouse

    Schulte, Ruth F.; Taylor, Ryan D.; Piatak, Nadine M.; Seal, Robert R.

    2010-01-01

    Stratiform chromite deposits are of great economic importance, yet their origin and evolution remain highly debated. Layered igneous intrusions such as the Bushveld, Great Dyke, Kemi, and Stillwater Complexes, provide opportunities for studying magmatic differentiation processes and assimilation within the crust, as well as related ore-deposit formation. Chromite-rich seams within layered intrusions host the majority of the world's chromium reserves and may contain significant platinum-group-element (PGE) mineralization. This model of stratiform chromite deposits is part of an effort by the U.S. Geological Survey's Mineral Resources Program to update existing models and develop new descriptive mineral deposit models to supplement previously published models for use in mineral-resource and mineral-environmental assessments. The model focuses on features that may be common to all stratiform chromite deposits as a way to gain insight into the processes that gave rise to their emplacement and to the significant economic resources contained in them.

  1. Gemstone deposits of Serbia

    NASA Astrophysics Data System (ADS)

    Miladinović, Zoran; Simić, Vladimir; Jelenković, Rade; Ilić, Miloje

    2016-06-01

    Gemstone minerals in Serbia have never been regarded as an interesting and significant resource. Nevertheless, more than 150 deposits and occurrences have been recorded and some of them preliminarily explored in the last 50 years. The majority of deposits and occurrences are located within the Serbo-Macedonian metallogenic province and the most significant metallogenic units at the existing level of knowledge are the Fruska Gora ore district, Cer ore district, Sumadija metallogenic zone, Kopaonik metallogenic zone and Lece-Halkidiki metallogenic zone. The most important genetic type of deposits is hydrothermal, particularly in case of serpentinite/peridotite as host/parent rock. Placer deposits are also economically important. The dominant gemstones are silica minerals: chalcedony (Chrysoprase, carnelian, bluish chalcedony etc.), jasper (picture, landscape, red etc.), common opal (dendritic, green, milky white etc.), silica masses (undivided), and quartz (rock crystal, amethyst etc.). Beside silica minerals significant gemstones in Serbia include also beryl (aquamarine), garnet (almandine and pyrope), tourmaline, fluorite, rhodochrosite, carbonate-silica breccia, carbonate-silica onyx, silicified wood, howlite, serpentinite, marble onyx, and kyanite. This paper aims to present an overview of Serbian gemstone deposits and occurrences and their position based on a simplified gemstone metallogenic map of Serbia, as well as genetic-industrial classification of gemstone deposits and gemstone varieties.

  2. To what extent can intracrater layered deposits that lack clear sedimentary textures be used to infer depositional environments?

    NASA Astrophysics Data System (ADS)

    Cadieux, Sarah B.; Kah, Linda C.

    2015-03-01

    Craters within Arabia Terra, Mars, contain hundreds of meters of layered strata showing systematic alternation between slope- and cliff-forming units, suggesting either rhythmic deposition of distinct lithologies or similar lithologies that experienced differential cementation. On Earth, rhythmically deposited strata can be examined in terms of stratal packaging, wherein the interplay of tectonics, sediment deposition, and base level (i.e., the position above which sediment accumulation is expected to be temporary) result in changes in the amount of space available for sediment accumulation. These predictable patterns of sediment deposition can be used to infer changes in basin accommodation regardless of the mechanism of deposition (e.g. fluvial, lacustrine, or aeolian). Here, we analyze sedimentary deposits from three craters (Becquerel Crater, Danielson Crater, Crater A) in Arabia Terra. Each crater contains layered deposits that are clearly observed in orbital images. Although orbital images are insufficient to specifically determine the origin of sedimentary deposits, depositional couplets can be interpreted in terms of potential accommodation space available for deposition, and changes in the distribution of couplet thickness through stratigraphy can be interpreted in terms of changing base level and the production of new accommodation space. Differences in stratal packaging in these three craters suggest varying relationships between sedimentary influx, sedimentary base level, and concomitant changes in accommodation space. Previous groundwater upwelling models hypothesize that layered sedimentary deposits were deposited under warm climate conditions of early Mars. Here, we use observed stacking patterns to propose a model for deposition under cold climate conditions, wherein episodic melting of ground ice could raise local base level, stabilize sediment deposition, and result in differential cementation of accumulated strata. Such analysis demonstrates that

  3. Seasonal atmospheric deposition variations of polychlorinated biphenyls (PCBs) and comparison of some deposition sampling techniques.

    PubMed

    Birgül, Askın; Tasdemir, Yücel

    2011-03-01

    Ambient air and bulk deposition samples were collected between June 2008 and June 2009. Eighty-three polychlorinated biphenyl (PCB) congeners were targeted in the samples. The average gas and particle PCB concentrations were found as 393 ± 278 and 70 ± 102 pg/m(3), respectively, and 85% of the atmospheric PCBs were in the gas phase. Bulk deposition samples were collected by using a sampler made of stainless steel. The average PCB bulk deposition flux value was determined as 6,020 ± 4,350 pg/m(2) day. The seasonal bulk deposition fluxes were not statistically different from each other, but the summer flux had higher values. Flux values differed depending on the precipitation levels. The average flux value in the rainy periods was 7,480 ± 4,080 pg/m(2) day while the average flux value in dry periods was 5,550 ± 4,420 pg/m(2) day. The obtained deposition values were lower than the reported values given for the urban and industrialized areas, yet close to the ones for the rural sites. The reported deposition values were also influenced by the type of the instruments used. The average dry deposition and total deposition velocity values calculated based on deposition and concentration values were found as 0.23 ± 0.21 and 0.13 ± 0.13 cm/s, respectively.

  4. Geochronology of the Thompson Creek Mo Deposit: Evidence for the Formation of Arc-related Mo Deposits

    NASA Astrophysics Data System (ADS)

    Lawrence, C. D.; Coleman, D. S.; Stein, H. J.

    2016-12-01

    The Thompson Creek Mo deposit in central ID, has been categorized as an arc-related Mo deposit due to the location, grade of Mo, and relative lack of enrichments in F, Rb, and Nb, compared to the Climax-type Mo deposits. Geochronology from this arc-related deposit provides an opportunity to compare and contrast magmatism, and mineralization to that in Climax-type deposits. Distinct pulses of magmatism were required to form the Thompson Creek Mo deposit, which is consistent with recent geochronology from Climax-type deposits. Molybdenite Re-Os geochronology from five veins requires at least three pulses of magmatism and mineralization between 89.39 +/- 0.37 and 88.47 +/- 0.16 Ma. Zircon U-Pb ages from these mineralized samples overlap with molybdenite mineralization, but show a much wider range (91.01 +/- 0.37 to 87.27 +/- 0.69). Previous work from Climax-type Mo deposits suggest a correlation between a super eruption, and the subsequent rapid (<1 Ma) onset, and completion of Mo mineralizing intrusions. The longer life (3-4 Ma) for the Thompson Creek Mo deposit suggests that the mineralizing intrusions for arc-related Mo deposits may not need to have as high [Mo] as the Climax-type deposits. This study also finds a shift in the source of magmatism from the pre- to syn-mineralizing intrusions. Zircons from pre-mineralizing intrusions have much higher (15-60 pg) concentrations of radiogenic Pb than zircons from mineralized intrusions, which all have less than 15 pg, though whole rock [U] are similar.

  5. 7 CFR 47.16 - Depositions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... which the deposition is to be conducted (telephone, audio-visual telecommunication, or by personal...) The place of the deposition; (iii) The manner of the deposition (telephone, audio-visual... shall be conducted in the manner (telephone, audio-visual telecommunication, or personal attendance of...

  6. Effect of heat treatment on the characteristics of tool steel deposited by the directed energy deposition process

    NASA Astrophysics Data System (ADS)

    Park, Jun Seok; Lee, Min-Gyu; Cho, Yong-Jae; Sung, Ji Hyun; Jeong, Myeong-Sik; Lee, Sang-Kon; Choi, Yong-Jin; Kim, Da Hye

    2016-01-01

    The directed energy deposition process has been mainly applied to re-work and the restoration of damaged steel. Differences in material properties between the base and the newly deposited materials are unavoidable, which may affect the mechanical properties and durability of the part. We investigated the effect of heat treatment on the characteristics of tool steel deposited by the DED process. We prepared general tool steel materials of H13 and D2 that were deposited onto heat-treated substrates of H13 and D2, respectively, using a direct metal tooling process. The hardness and microstructure of the deposited steel before and after heat treatment were investigated. The hardness of the deposited H13 steel was higher than that of wrought H13 steel substrate, while that of the deposited D2 was lower than that of wrought D2. The evolution of the microstructures by deposition and heat treatment varied depending on the materials. In particular, the microstructure of the deposited D2 steel after heat treatment consisted of fine carbides in tempered martensite and it is expected that the deposited D2 steel will have isotropic properties and high hardness after heat treatment.

  7. Modeling surficial sand and gravel deposits

    USGS Publications Warehouse

    Bliss, J.D.; Page, N.J.

    1994-01-01

    Mineral-deposit models are an integral part of quantitative mineral-resource assessment. As the focus of mineral-deposit modeling has moved from metals to industrial minerals, procedure has been modified and may be sufficient to model surficial sand and gravel deposits. Sand and gravel models are needed to assess resource-supply analyses for planning future development and renewal of infrastructure. Successful modeling of sand and gravel deposits must address (1) deposit volumes and geometries, (2) sizes of fragments within the deposits, (3) physical characteristics of the material, and (4) chemical composition and chemical reactivity of the material. Several models of sand and gravel volumes and geometries have been prepared and suggest the following: Sand and gravel deposits in alluvial fans have a median volume of 35 million m3. Deposits in all other geologic settings have a median volume of 5.4 million m3, a median area of 120 ha, and a median thickness of 4 m. The area of a sand and gravel deposit can be predicted from volume using a regression model (log [area (ha)] =1.47+0.79 log [volume (million m3)]). In similar fashion, the volume of a sand and gravel deposit can be predicted from area using the regression (log [volume (million m3)]=-1.45+1.07 log [area (ha)]). Classifying deposits by fragment size can be done using models of the percentage of sand, gravel, and silt within deposits. A classification scheme based on fragment size is sufficiently general to be applied anywhere. ?? 1994 Oxford University Press.

  8. 7 CFR 15.116 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 1 2010-01-01 2010-01-01 false Depositions. 15.116 Section 15.116 Agriculture Office... Depositions. Upon such terms as may be just, the hearing officer, in his discretion, may authorize the testimony of any witness to be taken by deposition. ...

  9. 7 CFR 15.116 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 7 Agriculture 1 2011-01-01 2011-01-01 false Depositions. 15.116 Section 15.116 Agriculture Office... Depositions. Upon such terms as may be just, the hearing officer, in his discretion, may authorize the testimony of any witness to be taken by deposition. ...

  10. Deposited films with improved microstructures

    DOEpatents

    Patten, James W.; Moss, Ronald W.; McClanahan, Edwin D.

    1984-01-01

    Methods for improving microstructures of line-of-sight deposited films are described. Columnar growth defects ordinarily produced by geometrical shadowing during deposition of such films are eliminated without resorting to post-deposition thermal or mechanical treatments. The native, as-deposited coating qualities, including homogeneity, fine grain size, and high coating-to-substrate adherence, can thus be retained. The preferred method includes the steps of emitting material from a source toward a substrate to deposit a coating non-uniformly on the substrate surface, removing a portion of the coating uniformly over the surface, again depositing material onto the surface, but from a different direction, and repeating the foregoing steps. The quality of line-of-sight deposited films such as those produced by sputtering, progressively deteriorates as the angle of incidence between the flux and the surface becomes increasingly acute. Depositing non-uniformly, so that the coating becomes progressively thinner as quality deteriorates, followed by uniformly removing some of the coating, such as by resputtering, eliminates the poor quality portions, leaving only high quality portions of the coating. Subsequently sputtering from a different direction applies a high quality coating to other regions of the surface. Such steps can be performed either simultaneously or sequentially to apply coatings of a uniformly high quality, closed microstructure to three-dimensional or large planar surfaces.

  11. 14 CFR 16.215 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 14 Aeronautics and Space 1 2010-01-01 2010-01-01 false Depositions. 16.215 Section 16.215... PRACTICE FOR FEDERALLY-ASSISTED AIRPORT ENFORCEMENT PROCEEDINGS Hearings § 16.215 Depositions. (a) General... deposition and that the witness produce documentary evidence in connection with such testimony. Generally, an...

  12. 14 CFR 16.215 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 14 Aeronautics and Space 1 2011-01-01 2011-01-01 false Depositions. 16.215 Section 16.215... PRACTICE FOR FEDERALLY-ASSISTED AIRPORT ENFORCEMENT PROCEEDINGS Hearings § 16.215 Depositions. (a) General... deposition and that the witness produce documentary evidence in connection with such testimony. Generally, an...

  13. 45 CFR 81.76 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 45 Public Welfare 1 2011-10-01 2011-10-01 false Depositions. 81.76 Section 81.76 Public Welfare... 80 OF THIS TITLE Hearing Procedures § 81.76 Depositions. Upon such terms as may be just, for the... of any witness to be taken by deposition. ...

  14. 45 CFR 81.76 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Depositions. 81.76 Section 81.76 Public Welfare... 80 OF THIS TITLE Hearing Procedures § 81.76 Depositions. Upon such terms as may be just, for the... of any witness to be taken by deposition. ...

  15. 49 CFR 510.6 - Administrative depositions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 6 2011-10-01 2011-10-01 false Administrative depositions. 510.6 Section 510.6... ADMINISTRATION, DEPARTMENT OF TRANSPORTATION INFORMATION GATHERING POWERS § 510.6 Administrative depositions. (a... entity to provide information as a witness at an administrative deposition. These depositions are for the...

  16. 40 CFR 1610.4 - Deposition Transcripts.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 32 2010-07-01 2010-07-01 false Deposition Transcripts. 1610.4 Section... INVESTIGATIONS § 1610.4 Deposition Transcripts. (a) Transcripts of depositions of witnesses compelled by subpoena... by the person conducting the deposition. (b) Such a witness, after completing the compelled testimony...

  17. 40 CFR 1610.4 - Deposition Transcripts.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 33 2011-07-01 2011-07-01 false Deposition Transcripts. 1610.4 Section... INVESTIGATIONS § 1610.4 Deposition Transcripts. (a) Transcripts of depositions of witnesses compelled by subpoena... by the person conducting the deposition. (b) Such a witness, after completing the compelled testimony...

  18. Ore Deposits Mined for Critical Elements

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

    Verplanck, Philip; Kelley, Karen

    Summary of deposit types containing critical elements, including, cobalt, gallium, germanium, indium, niobium, PGE, REE, rhenium, selenium, and tellurium. Includes information about ore deposit type, mineralogy, geologic setting, example deposits and districts, concentration ranges per reported resource, grade, and additional deposit notes. References are also included.

  19. Global deposition of airborne dioxin.

    PubMed

    Booth, Shawn; Hui, Joe; Alojado, Zoraida; Lam, Vicky; Cheung, William; Zeller, Dirk; Steyn, Douw; Pauly, Daniel

    2013-10-15

    We present a global dioxin model that simulates one year of atmospheric emissions, transport processes, and depositions to the earth's terrestrial and marine habitats. We map starting emission levels for each land area, and we also map the resulting deposits to terrestrial and marine environments. This model confirms that 'hot spots' of deposition are likely to be in northern Europe, eastern North America, and in parts of Asia with the highest marine dioxin depositions being the northeast and northwest Atlantic, western Pacific, northern Indian Ocean and the Mediterranean. It also reveals that approximately 40% of airborne dioxin emissions are deposited to marine environments and that many countries in Africa receive more dioxin than they produce, which results in these countries being disproportionately impacted. Since human exposure to dioxin is largely through diet, this work highlights food producing areas that receive higher atmospheric deposits of dioxin than others. Copyright © 2013 Elsevier Ltd. All rights reserved.

  20. Mineral deposit densities for estimating mineral resources

    USGS Publications Warehouse

    Singer, Donald A.

    2008-01-01

    Estimates of numbers of mineral deposits are fundamental to assessing undiscovered mineral resources. Just as frequencies of grades and tonnages of well-explored deposits can be used to represent the grades and tonnages of undiscovered deposits, the density of deposits (deposits/area) in well-explored control areas can serve to represent the number of deposits. Empirical evidence presented here indicates that the processes affecting the number and quantity of resources in geological settings are very general across many types of mineral deposits. For podiform chromite, porphyry copper, and volcanogenic massive sulfide deposit types, the size of tract that geologically could contain the deposits is an excellent predictor of the total number of deposits. The number of mineral deposits is also proportional to the type’s size. The total amount of mineralized rock is also proportional to size of the permissive area and the median deposit type’s size. Regressions using these variables provide a means to estimate the density of deposits and the total amount of mineralization. These powerful estimators are based on analysis of ten different types of mineral deposits (Climax Mo, Cuban Mn, Cyprus massive sulfide, Franciscan Mn, kuroko massive sulfide, low-sulfide quartz-Au vein, placer Au, podiform Cr, porphyry Cu, and W vein) from 108 permissive control tracts around the world therefore generalizing across deposit types. Despite the diverse and complex geological settings of deposit types studied here, the relationships observed indicate universal controls on the accumulation and preservation of mineral resources that operate across all scales. The strength of the relationships (R 2=0.91 for density and 0.95 for mineralized rock) argues for their broad use. Deposit densities can now be used to provide a guideline for expert judgment or used directly for estimating the number of most kinds of mineral deposits.

  1. 49 CFR 1114.22 - Deposition.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 8 2010-10-01 2010-10-01 false Deposition. 1114.22 Section 1114.22 Transportation... TRANSPORTATION RULES OF PRACTICE EVIDENCE; DISCOVERY Discovery § 1114.22 Deposition. (a) Purpose. The testimony of any person, including a party, may be taken by deposition upon oral examination. (b) Request. A...

  2. 10 CFR 2.1019 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 1 2011-01-01 2011-01-01 false Depositions. 2.1019 Section 2.1019 Energy NUCLEAR... Geologic Repository § 2.1019 Depositions. (a) Any party or interested governmental participant desiring to take the testimony of any person by deposition on oral examination shall, without leave of the...

  3. 10 CFR 2.1019 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 1 2010-01-01 2010-01-01 false Depositions. 2.1019 Section 2.1019 Energy NUCLEAR... Geologic Repository § 2.1019 Depositions. (a) Any party or interested governmental participant desiring to take the testimony of any person by deposition on oral examination shall, without leave of the...

  4. 34 CFR 101.76 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 34 Education 1 2011-07-01 2011-07-01 false Depositions. 101.76 Section 101.76 Education... PRACTICE AND PROCEDURE FOR HEARINGS UNDER PART 100 OF THIS TITLE Hearing Procedures § 101.76 Depositions... officer may authorize or direct the testimony of any witness to be taken by deposition. ...

  5. 49 CFR 1114.22 - Deposition.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 8 2011-10-01 2011-10-01 false Deposition. 1114.22 Section 1114.22 Transportation... TRANSPORTATION RULES OF PRACTICE EVIDENCE; DISCOVERY Discovery § 1114.22 Deposition. (a) Purpose. The testimony of any person, including a party, may be taken by deposition upon oral examination. (b) Request. A...

  6. 34 CFR 101.76 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 34 Education 1 2010-07-01 2010-07-01 false Depositions. 101.76 Section 101.76 Education... PRACTICE AND PROCEDURE FOR HEARINGS UNDER PART 100 OF THIS TITLE Hearing Procedures § 101.76 Depositions... officer may authorize or direct the testimony of any witness to be taken by deposition. ...

  7. 37 CFR 11.51 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2011-07-01 2011-07-01 false Depositions. 11.51 Section 11... Disciplinary Proceedings; Jurisdiction, Sanctions, Investigations, and Proceedings § 11.51 Depositions. (a) Depositions for use at the hearing in lieu of personal appearance of a witness before the hearing officer may...

  8. Translocation of the retinal pigment epithelium and formation of sub-retinal pigment epithelium deposit induced by subretinal deposit

    PubMed Central

    Zhao, Lian; Wang, Zhenfang; Liu, Yun; Song, Ying; Li, Yiwen; Laties, Alan M.

    2007-01-01

    Purpose A cardinal pathological feature of age-related macular degeneration (AMD) is the deposition of extracellular material between the retinal pigment epithelium (RPE) and Bruch's membrane, pathologically described as sub-RPE deposits. Both the presence and local organization of these deposits contribute to the clinical manifestations of AMD, including localized deposits clinically recognized as drusen. The biogenesis of sub-RPE deposits remains elusive. This work explores the pathological processes of sub-RPE deposit formation. Methods Matrigel was injected to the subretinal space of rats to create an amorphous deposit. Tissue sections were examined by light or confocal microscopy. Results In the presence of the subretinal deposit of Matrigel, RPE cells leave Bruch's membrane to migrate toward photoreceptors and then form a new layer between the deposit and photoreceptors, resulting in RPE translocation. The new RPE layer displaces the deposit to the sub-RPE location and therefore it becomes a sub-RPE deposit. The RPE mobilization requires the presence of photoreceptors. Bruch's membrane devoid of RPE attachment becomes vulnerable to invasion by new blood vessels from the choroid. Conclusions Our work supports a novel model of sub-RPE deposit formation in which excessive material first accumulates in the subretinal space, disrupting the physical contact between RPE cells and photoreceptors. To restore the contact, RPE cells migrate toward photoreceptors and form a new layer. The subretinal material is consequently displaced to the sub-RPE location and becomes sub-RPE deposit. Our data also provide evidence that the presence of sub-RPE deposit is sufficient to induce choroidal neovascularization to penetrate Bruch's membrane. PMID:17615538

  9. Chemical bath deposited and dip coating deposited CuS thin films - Structure, Raman spectroscopy and surface study

    NASA Astrophysics Data System (ADS)

    Tailor, Jiten P.; Khimani, Ankurkumar J.; Chaki, Sunil H.

    2018-05-01

    The crystal structure, Raman spectroscopy and surface microtopography study on as-deposited CuS thin films were carried out. Thin films deposited by two techniques of solution growth were studied. The thin films used in the present study were deposited by chemical bath deposition (CBD) and dip coating deposition techniques. The X-ray diffraction (XRD) analysis of both the as-deposited thin films showed that both the films possess covellite phase of CuS and hexagonal unit cell structure. The determined lattice parameters of both the films are in agreement with the standard JCPDS as well as reported data. The crystallite size determined by Scherrer's equation and Hall-Williamsons relation using XRD data for both the as-deposited thin films showed that the respective values were in agreement with each other. The ambient Raman spectroscopy of both the as-deposited thin films showed major emission peaks at 474 cm-1 and a minor emmision peaks at 265 cm-1. The observed Raman peaks matched with the covellite phase of CuS. The atomic force microscopy of both the as-deposited thin films surfaces showed dip coating thin film to be less rough compared to CBD deposited thin film. All the obtained results are presented and deliberated in details.

  10. Chemotrophic Microbial Mats and Their Potential for Preservation in the Rock Record

    NASA Astrophysics Data System (ADS)

    Bailey, Jake V.; Orphan, Victoria J.; Joye, Samantha B.; Corsetti, Frank A.

    2009-11-01

    Putative microbialites are commonly regarded to have formed in association with photosynthetic microorganisms, such as cyanobacteria. However, many modern microbial mat ecosystems are dominated by chemotrophic bacteria and archaea. Like phototrophs, filamentous sulfur-oxidizing bacteria form large mats at the sediment/water interface that can act to stabilize sediments, and their metabolic activities may mediate the formation of marine phosphorites. Similarly, bacteria and archaea associated with the anaerobic oxidation of methane (AOM) catalyze the precipitation of seafloor authigenic carbonates. When preserved, lipid biomarkers, isotopic signatures, body fossils, and lithological indicators of the local depositional environment may be used to identify chemotrophic mats in the rock record. The recognition of chemotrophic communities in the rock record has the potential to transform our understanding of ancient microbial ecologies, evolution, and geochemical conditions. Chemotrophic microbes on Earth occupy naturally occurring interfaces between oxidized and reduced chemical species and thus may provide a new set of search criteria to target life-detection efforts on other planets.

  11. Simultaneous ion sputter polishing and deposition

    NASA Technical Reports Server (NTRS)

    Rutledge, S.; Banks, B.; Brdar, M.

    1981-01-01

    Results of experiments to study ion beam sputter polishing in conjunction with simultaneous deposition as a mean of polishing copper surfaces are presented. Two types of simultaneous ion sputter polishing and deposition were used in these experiments. The first type utilized sputter polishing simultaneous with vapor deposition, and the second type utilized sputter polishing simultaneous with sputter deposition. The etch and deposition rates of both techniques were studied, as well as the surface morphology and surface roughness.

  12. 24 CFR 891.635 - Security deposits.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 24 Housing and Urban Development 4 2013-04-01 2013-04-01 false Security deposits. 891.635 Section... Assistance § 891.635 Security deposits. The general requirements for security deposits on assisted units are... a security deposit equal to one month's rent payable by the family. (b) The Borrower shall maintain...

  13. 16 CFR 3.33 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 16 Commercial Practices 1 2010-01-01 2010-01-01 false Depositions. 3.33 Section 3.33 Commercial... ADJUDICATIVE PROCEEDINGS Discovery; Compulsory Process § 3.33 Depositions. (a) In general. Any party may take a deposition of any named person or of a person or persons described with reasonable particularity, provided...

  14. 16 CFR 3.33 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 16 Commercial Practices 1 2011-01-01 2011-01-01 false Depositions. 3.33 Section 3.33 Commercial... ADJUDICATIVE PROCEEDINGS Discovery; Compulsory Process § 3.33 Depositions. (a) In general. Any party may take a deposition of any named person or of a person or persons described with reasonable particularity, provided...

  15. 49 CFR 604.39 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 7 2011-10-01 2011-10-01 false Depositions. 604.39 Section 604.39 Transportation... TRANSPORTATION CHARTER SERVICE Hearings. § 604.39 Depositions. (a) For good cause shown, the PO may order that the testimony of a witness may be taken by deposition and that the witness produce documentary...

  16. 29 CFR 2700.57 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 9 2010-07-01 2010-07-01 false Depositions. 2700.57 Section 2700.57 Labor Regulations... § 2700.57 Depositions. (a) Generally. Any party, without leave of the Judge, may take the testimony of any person, including a party, by deposition upon oral examination or written interrogatories. (b...

  17. 29 CFR 2700.57 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 9 2011-07-01 2011-07-01 false Depositions. 2700.57 Section 2700.57 Labor Regulations... § 2700.57 Depositions. (a) Generally. Any party, without leave of the Judge, may take the testimony of any person, including a party, by deposition upon oral examination or written interrogatories. (b...

  18. 49 CFR 604.39 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 7 2010-10-01 2010-10-01 false Depositions. 604.39 Section 604.39 Transportation... TRANSPORTATION CHARTER SERVICE Hearings. § 604.39 Depositions. (a) For good cause shown, the PO may order that the testimony of a witness may be taken by deposition and that the witness produce documentary...

  19. Aerosol Deposition in Health and Disease

    PubMed Central

    2012-01-01

    Abstract The success of inhalation therapy is not only dependent upon the pharmacology of the drugs being inhaled but also upon the site and extent of deposition in the respiratory tract. This article reviews the main mechanisms affecting the transport and deposition of inhaled aerosol in the human lung. Aerosol deposition in both the healthy and diseased lung is described mainly based on the results of human studies using nonimaging techniques. This is followed by a discussion of the effect of flow regime on aerosol deposition. Finally, the link between therapeutic effects of inhaled drugs and their deposition pattern is briefly addressed. Data show that total lung deposition is a poor predictor of clinical outcome, and that regional deposition needs to be assessed to predict therapeutic effectiveness. Indeed, spatial distribution of deposited particles and, as a consequence, drug efficiency is strongly affected by particle size. Large particles (>6 μm) tend to mainly deposit in the upper airway, limiting the amount of drugs that can be delivered to the lung. Small particles (<2 μm) deposit mainly in the alveolar region and are probably the most apt to act systemically, whereas the particle in the size range 2–6 μm are be best suited to treat the central and small airways. PMID:22686623

  20. Mississippi Valley-Type Lead-Zinc Deposit Model

    USGS Publications Warehouse

    Leach, David L.; Taylor, Ryan D.

    2009-01-01

    Mississippi Valley-type (MVT) lead-zinc (Pb+Zn) deposits are found throughout the world, and these deposits are characteristically distributed over hundreds of square kilometers that define individual ore districts. The median size of individual MVT deposits is 7.0 million tonnes with grades of about 7.9 percent Pb+Zn metal. However, MVT deposits usually occur in extensive districts consisting of several to as many as 400 deposits. Nearly one-quarter of the world's sedimentary and volcanic rock-hosted Pb+Zn resources are found in these deposits, with by-product commodities including silver (Ag), copper (Cu), and indium (In) for some deposits. Environmentally, MVT deposits are less of a concern than other types of mineral deposits since the carbonate-host rocks mitigate many environmental concerns.

  1. Template-directed deposition of amyloid

    NASA Astrophysics Data System (ADS)

    Ha, Chanki

    The formation of amyloid plaques in tissue is a pathological feature of many neurodegenerative diseases. Amyloid deposition, the process of amyloid plaque growth by the association of individual soluble amyloid molecules with a pre-existing amyloid template (i.e. plaque), is known to be critical for amyloid formation in vivo. In order to characterize amyloid deposition, we developed novel, synthetic amyloid templates like amyloid plaques in the human Alzheimer's brain by attaching amyloid seeds covalently onto an N-hydroxysuccinimide-activated surface. Amyloid plaques with a characteristic beta-sheet structure formed through a conformational rearrangement of soluble insulin or Abeta monomers upon interaction with the template. The amyloid deposition rate followed saturation kinetics with respect to insulin concentration in the solution. According to visualization of temporal evolution of Abeta plaque deposition on a template, it was found that mature amyloid plaques serve as a sink of soluble Abeta in a solution as well as a reservoir of small aggregates such as oligomers and protofibrils. Quantitative analysis of seeding efficiencies of three different Abeta species revealed that oligomeric forms of Abeta act more efficiently as seeds than monomers or fibrils do. Furthermore, studies on the interaction between Abeta40 and 42 showed an important role of Abeta42 in amyloid deposition. A slightly acidic condition was found to be unfavorable for amyloid plaque formation. Effects of metal ions on amyloid deposition indicated that Fe3+, but not Cu3 and Zn2+, is important for the deposition of amyloid plaques. The binding of Fe3+ to Abeta42 peptide was confirmed by using SIMS analysis. Zn2+ induced nonfibrillar amorphous aggregates, but the release of Zn2+ from Abeta42 deposits by Fe3+ triggered the formation of amyloid fibers. Effects or metal ion chelators such as ethylenediamine tetraacetic acid, deferoxamine, and clioquinol on amyloid deposition were tested to

  2. 50 CFR 259.34 - Minimum and maximum deposits; maximum time to deposit.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... B objective. A time longer than 10 years, either by original scheduling or by subsequent extension... OCEANIC AND ATMOSPHERIC ADMINISTRATION, DEPARTMENT OF COMMERCE AID TO FISHERIES CAPITAL CONSTRUCTION FUND...) Minimum annual deposit. The minimum annual (based on each party's taxable year) deposit required by the...

  3. 12 CFR 19.171 - Deposition subpoenas.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Deposition subpoenas. 19.171 Section 19.171... PROCEDURE Discovery Depositions and Subpoenas § 19.171 Deposition subpoenas. (a) Issuance. At the request of... at a discovery deposition under paragraph (a) of this section. The attendance of a witness may be...

  4. 31 CFR 15.737-22 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 31 Money and Finance: Treasury 1 2010-07-01 2010-07-01 false Depositions. 15.737-22 Section 15.737... INTEREST Administrative Enforcement Proceedings § 15.737-22 Depositions. Depositions for use at a hearing.... Depositions may be taken upon oral or written interrogatories, upon not less than 10 days' written notice to...

  5. 12 CFR 19.171 - Deposition subpoenas.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Deposition subpoenas. 19.171 Section 19.171... PROCEDURE Discovery Depositions and Subpoenas § 19.171 Deposition subpoenas. (a) Issuance. At the request of... at a discovery deposition under paragraph (a) of this section. The attendance of a witness may be...

  6. 31 CFR 15.737-22 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 31 Money and Finance: Treasury 1 2011-07-01 2011-07-01 false Depositions. 15.737-22 Section 15.737... INTEREST Administrative Enforcement Proceedings § 15.737-22 Depositions. Depositions for use at a hearing.... Depositions may be taken upon oral or written interrogatories, upon not less than 10 days' written notice to...

  7. 12 CFR 19.170 - Discovery depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Discovery depositions. 19.170 Section 19.170... PROCEDURE Discovery Depositions and Subpoenas § 19.170 Discovery depositions. (a) General rule. In any... deposition of an expert, or of a person, including another party, who has direct knowledge of matters that...

  8. 12 CFR 19.170 - Discovery depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 1 2011-01-01 2011-01-01 false Discovery depositions. 19.170 Section 19.170... PROCEDURE Discovery Depositions and Subpoenas § 19.170 Discovery depositions. (a) General rule. In any... deposition of an expert, or of a person, including another party, who has direct knowledge of matters that...

  9. 46 CFR 287.11 - Time deposits.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 8 2014-10-01 2014-10-01 false Time deposits. 287.11 Section 287.11 Shipping MARITIME... OF CONSTRUCTION RESERVE FUNDS § 287.11 Time deposits. Deposits in the construction reserve fund not invested in securities may be placed in time deposits when, in the judgment of the taxpayer, it is...

  10. 46 CFR 287.11 - Time deposits.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 46 Shipping 8 2012-10-01 2012-10-01 false Time deposits. 287.11 Section 287.11 Shipping MARITIME... OF CONSTRUCTION RESERVE FUNDS § 287.11 Time deposits. Deposits in the construction reserve fund not invested in securities may be placed in time deposits when, in the judgment of the taxpayer, it is...

  11. 46 CFR 287.11 - Time deposits.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 8 2011-10-01 2011-10-01 false Time deposits. 287.11 Section 287.11 Shipping MARITIME... OF CONSTRUCTION RESERVE FUNDS § 287.11 Time deposits. Deposits in the construction reserve fund not invested in securities may be placed in time deposits when, in the judgment of the taxpayer, it is...

  12. 46 CFR 287.11 - Time deposits.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 8 2013-10-01 2013-10-01 false Time deposits. 287.11 Section 287.11 Shipping MARITIME... OF CONSTRUCTION RESERVE FUNDS § 287.11 Time deposits. Deposits in the construction reserve fund not invested in securities may be placed in time deposits when, in the judgment of the taxpayer, it is...

  13. Metallogenic evolution of uranium deposits in the Middle East and North Africa deposits

    NASA Astrophysics Data System (ADS)

    Howari, Fares; Goodell, Philip; Salman, Abdulaty

    2016-02-01

    This paper is briefly involved in classification and distributions of the Middle East and North Africa (MENA) uranium deposits. The study of these mineral systems can significantly contribute to our further understanding of the metallogeny of known and poorly explored deposits. This provides contribution to, and further enhancement of, current classifications and metallogenic models of uranium systems, allowing researchers to emphasize on unknown or poorly studied mineral systems found in MENA. The present study identified eight metallogenic types of uranium associated with: 1) the Archean rocks and intra-cratonic basins, 2) the Pan-African granites and rhyolites which are characterized by igneous activity, 3) Phanerozoic (Paleozoic) clastics, these deposits are the sedimentological response to Pan African magmatism, 4) Mesozoic (basal) clastics type e.g. Nubia sandstones which are characterized by uranium minerals, 5) regional sedimentary phosphate deposits which are categorized as geosynclinal, or continental margin deposits, on the shelf of the Tethys Ocean, 6) Cenozoic Intracratonic Felsic Magmatism of the Tibesti and Hoggar, and the sandstone U deposits of adjoining Niger. These are similar to the Pan-African magmatism metallogenic, 7) Calcretes, and 8) Resistate minerals which are often enriched in rare earth elements, sometimes including uranium. They are thus sometimes considered as U resources but poorly explored in the MENA region. These metallogenic types are described and discussed in the current paper.

  14. 8 CFR 341.3 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 8 Aliens and Nationality 1 2011-01-01 2011-01-01 false Depositions. 341.3 Section 341.3 Aliens and... Depositions. If satisfied that a witness whose testimony is essential is not available for examination in the United States, the assigned officer may authorize the taking of a deposition abroad by written...

  15. 10 CFR 590.307 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 4 2011-01-01 2011-01-01 false Depositions. 590.307 Section 590.307 Energy DEPARTMENT OF... RESPECT TO THE IMPORT AND EXPORT OF NATURAL GAS Procedures § 590.307 Depositions. (a) Upon motion filed by... witness by deposition. Unless otherwise directed in the authorization issued, a witness being deposed may...

  16. 28 CFR 68.22 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 28 Judicial Administration 2 2010-07-01 2010-07-01 false Depositions. 68.22 Section 68.22 Judicial... IMMIGRATION-RELATED EMPLOYMENT PRACTICES, AND DOCUMENT FRAUD § 68.22 Depositions. (a) Notice. Any party desiring to take the deposition of a witness shall give notice in writing to the witness and other parties...

  17. 14 CFR 13.53 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 14 Aeronautics and Space 1 2011-01-01 2011-01-01 false Depositions. 13.53 Section 13.53... INVESTIGATIVE AND ENFORCEMENT PROCEDURES Rules of Practice for FAA Hearings § 13.53 Depositions. After the respondent has filed a request for hearing and an answer, either party may take testimony by deposition in...

  18. 8 CFR 342.6 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 8 Aliens and Nationality 1 2010-01-01 2010-01-01 false Depositions. 342.6 Section 342.6 Aliens and... CERTIFICATES, DOCUMENTS, OR RECORDS § 342.6 Depositions. Upon good cause shown, the testimony of any witness may be taken by depositions, either orally or upon written interrogatories before a person having...

  19. 8 CFR 341.3 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 8 Aliens and Nationality 1 2010-01-01 2010-01-01 false Depositions. 341.3 Section 341.3 Aliens and... Depositions. If satisfied that a witness whose testimony is essential is not available for examination in the United States, the assigned officer may authorize the taking of a deposition abroad by written...

  20. 14 CFR 13.53 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 14 Aeronautics and Space 1 2010-01-01 2010-01-01 false Depositions. 13.53 Section 13.53... INVESTIGATIVE AND ENFORCEMENT PROCEDURES Rules of Practice for FAA Hearings § 13.53 Depositions. After the respondent has filed a request for hearing and an answer, either party may take testimony by deposition in...

  1. 8 CFR 342.6 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 8 Aliens and Nationality 1 2011-01-01 2011-01-01 false Depositions. 342.6 Section 342.6 Aliens and... CERTIFICATES, DOCUMENTS, OR RECORDS § 342.6 Depositions. Upon good cause shown, the testimony of any witness may be taken by depositions, either orally or upon written interrogatories before a person having...

  2. 28 CFR 68.22 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 28 Judicial Administration 2 2011-07-01 2011-07-01 false Depositions. 68.22 Section 68.22 Judicial... IMMIGRATION-RELATED EMPLOYMENT PRACTICES, AND DOCUMENT FRAUD § 68.22 Depositions. (a) Notice. Any party desiring to take the deposition of a witness shall give notice in writing to the witness and other parties...

  3. 39 CFR 957.18 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 39 Postal Service 1 2010-07-01 2010-07-01 false Depositions. 957.18 Section 957.18 Postal Service... SUSPENSION FROM CONTRACTING § 957.18 Depositions. (a) Not later than 7 days prior to the scheduled date of the hearing any party may file application with the Recorder for the taking of testimony by deposition...

  4. 24 CFR 180.515 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 24 Housing and Urban Development 1 2010-04-01 2010-04-01 false Depositions. 180.515 Section 180... Depositions. (a) Notice. Upon written notice to the witness and to all other parties, a party may take the testimony of a witness by deposition and may request the production of specified documents or materials by...

  5. 39 CFR 959.20 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 39 Postal Service 1 2011-07-01 2011-07-01 false Depositions. 959.20 Section 959.20 Postal Service... STATUTES § 959.20 Depositions. (a) Not later than 5 days after the filing of respondent's answer, any party may file an application with the Recorder for the taking of testimony by deposition. In support of...

  6. 24 CFR 180.515 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 24 Housing and Urban Development 1 2011-04-01 2011-04-01 false Depositions. 180.515 Section 180... Depositions. (a) Notice. Upon written notice to the witness and to all other parties, a party may take the testimony of a witness by deposition and may request the production of specified documents or materials by...

  7. 29 CFR 1921.19 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 7 2010-07-01 2010-07-01 false Depositions. 1921.19 Section 1921.19 Labor Regulations...' COMPENSATION ACT Miscellaneous § 1921.19 Depositions. (a) When, how, and by whom taken. For good cause shown, the testimony of any witness may be taken by deposition in any proceeding, when a complaint has been...

  8. 14 CFR 302.26 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 14 Aeronautics and Space 4 2011-01-01 2011-01-01 false Depositions. 302.26 Section 302.26... Proceedings § 302.26 Depositions. (a) For good cause shown, the DOT decisionmaker or administrative law judge assigned to a proceeding may order that the testimony of a witness be taken by deposition and that the...

  9. 39 CFR 959.20 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 39 Postal Service 1 2010-07-01 2010-07-01 false Depositions. 959.20 Section 959.20 Postal Service... STATUTES § 959.20 Depositions. (a) Not later than 5 days after the filing of respondent's answer, any party may file an application with the Recorder for the taking of testimony by deposition. In support of...

  10. 43 CFR 4.827 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false Depositions. 4.827 Section 4.827 Public... the Interior-Effectuation of Title VI of the Civil Rights Act of 1964 Procedures § 4.827 Depositions. (a) A party may take the testimony of any person, including a party, by deposition upon oral...

  11. 43 CFR 4.827 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 1 2011-10-01 2011-10-01 false Depositions. 4.827 Section 4.827 Public... the Interior-Effectuation of Title VI of the Civil Rights Act of 1964 Procedures § 4.827 Depositions. (a) A party may take the testimony of any person, including a party, by deposition upon oral...

  12. 29 CFR 1921.19 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 7 2011-07-01 2011-07-01 false Depositions. 1921.19 Section 1921.19 Labor Regulations...' COMPENSATION ACT Miscellaneous § 1921.19 Depositions. (a) When, how, and by whom taken. For good cause shown, the testimony of any witness may be taken by deposition in any proceeding, when a complaint has been...

  13. 14 CFR 302.26 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 14 Aeronautics and Space 4 2010-01-01 2010-01-01 false Depositions. 302.26 Section 302.26... Proceedings § 302.26 Depositions. (a) For good cause shown, the DOT decisionmaker or administrative law judge assigned to a proceeding may order that the testimony of a witness be taken by deposition and that the...

  14. 39 CFR 957.18 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 39 Postal Service 1 2011-07-01 2011-07-01 false Depositions. 957.18 Section 957.18 Postal Service... SUSPENSION FROM CONTRACTING § 957.18 Depositions. (a) Not later than 7 days prior to the scheduled date of the hearing any party may file application with the Recorder for the taking of testimony by deposition...

  15. 49 CFR 604.39 - Depositions.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... deposition is deemed necessary to perpetuate the testimony of the witness; or (3) The taking of the...; (2) The time and place for the taking of the proposed deposition; (3) The reasons why such deposition... waive the signing, or the witness is ill, cannot be found, or refuses to sign. The reporter shall note...

  16. 49 CFR 604.39 - Depositions.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... deposition is deemed necessary to perpetuate the testimony of the witness; or (3) The taking of the...; (2) The time and place for the taking of the proposed deposition; (3) The reasons why such deposition... waive the signing, or the witness is ill, cannot be found, or refuses to sign. The reporter shall note...

  17. 49 CFR 604.39 - Depositions.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... deposition is deemed necessary to perpetuate the testimony of the witness; or (3) The taking of the...; (2) The time and place for the taking of the proposed deposition; (3) The reasons why such deposition... waive the signing, or the witness is ill, cannot be found, or refuses to sign. The reporter shall note...

  18. A study of carbon deposition on fuel cell power plants — morphology of deposited carbon and catalytic metal in carbon deposition reactions on stainless steel

    NASA Astrophysics Data System (ADS)

    Sone, Yuko; Kishida, Haruo; Kobayashi, Makoto; Watanabe, Takao

    Carbon deposited on SUS304 stainless steel (18Cr 8Ni) has been observed by two different methods. One method was Field Emission Transmission Electron Microscopy (FE-TEM), with developed preparation for in situ observation of a cross-section of the deposited carbon from the base (SUS) to the top. The other method was X-ray Photoelectron Spectroscopy (XPS), obtaining composition-depth profiles by argon ion sputtering. Carbon was deposited on SUS304, 550°C, 1 atm, H 2/CO/CO 2=75/15/10, after drained the steam-reformed natural gas composition. One result from FE-TEM identified the major form of deposited carbon was tubular in shape with a variety of diameters, ranging from approximately 7 to 100 nm. Some tubes contained metallic particles which were about 20 nm in size at their tips. Therefore, it can be established that the carbon deposition mechanism is similar to that reported for metals such as Fe, Ni, and that the deposited carbon can grow after the SUS surface is covered with deposits under the above conditions. Observations from EDX attached to FE-TEM also determined that most of the particles consisted of Fe and from XPS, that the content of Fe on the surface of the reaction plate was lower than on the unreacted sample. This indicates that carbon deposition on stainless steel was influenced by Fe rather than Ni and Cr.

  19. Hydroxyapatite Deposition Disease

    DTIC Science & Technology

    2006-11-01

    site of HADD is the hip, where calcifications are usually found in the gluteus medius tendon or along the femur at various sites of tendinous ...characterized by deposition of calcium phosphate crystals in periarticular tissues. The deposits frequently occur in tendons near their osseous...attachments, most commonly involving the supraspinatus tendon . The etiology of HADD is unclear, but may be related to repetitive trauma or metabolic

  20. Mechanics of hydrogenated amorphous carbon deposits from electron-beam-induced deposition of a paraffin precursor

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

    Ding, W.; Dikin, D.A.; Chen, X.

    2005-07-01

    Many experiments on the mechanics of nanostructures require the creation of rigid clamps at specific locations. In this work, electron-beam-induced deposition (EBID) has been used to deposit carbon films that are similar to those that have recently been used for clamping nanostructures. The film deposition rate was accelerated by placing a paraffin source of hydrocarbon near the area where the EBID deposits were made. High-resolution transmission electron microscopy, electron-energy-loss spectroscopy, Raman spectroscopy, secondary-ion-mass spectrometry, and nanoindentation were used to characterize the chemical composition and the mechanics of the carbonaceous deposits. The typical EBID deposit was found to be hydrogenated amorphousmore » carbon (a-C:H) having more sp{sup 2}- than sp{sup 3}-bonded carbon. Nanoindentation tests revealed a hardness of {approx}4 GPa and an elastic modulus of 30-60 GPa, depending on the accelerating voltage. This reflects a relatively soft film, which is built out of precursor molecular ions impacting the growing surface layer with low energies. The use of such deposits as clamps for tensile tests of poly(acrylonitrile)-based carbon nanofibers loaded between opposing atomic force microscope cantilevers is presented as an example application.« less

  1. EDITORIAL: Atomic layer deposition Atomic layer deposition

    NASA Astrophysics Data System (ADS)

    Godlewski, Marek

    2012-07-01

    The growth method of atomic layer deposition (ALD) was introduced in Finland by Suntola under the name of atomic layer epitaxy (ALE). The method was originally used for deposition of thin films of sulphides (ZnS, CaS, SrS) activated with manganese or rare-earth ions. Such films were grown for applications in thin-film electroluminescence (TFEL) displays. The ALE mode of growth was also tested in the case of molecular beam epitaxy. Films grown by ALD are commonly polycrystalline or even amorphous. Thus, the name ALE has been replaced by ALD. In the 80s ALD was developed mostly in Finland and neighboring Baltic countries. Deposition of a range of different materials was demonstrated at that time, including II-VI semiconductors (e.g. CdTe, CdS) and III-V (e.g. GaAs, GaN), with possible applications in e.g. photovoltaics. The number of publications on ALD was slowly increasing, approaching about 100 each year. A real boom in interest came with the development of deposition methods of thin films of high-k dielectrics. This research was motivated by a high leakage current in field-effect transistors with SiO2-based gate dielectrics. In 2007 Intel introduced a new generation of integrated circuits (ICs) with thin films of HfO2 used as gate isolating layers. In these and subsequent ICs, films of HfO2 are deposited by the ALD method. This is due to their unique properties. The introduction of ALD to the electronics industry led to a booming interest in the ALD growth method, with the number of publications increasing rapidly to well above 1000 each year. A number of new applications were proposed, as reflected in this special issue of Semiconductor Science and Technology. The included articles cover a wide range of possible applications—in microelectronics, transparent electronics, optoelectronics, photovoltaics and spintronics. Research papers and reviews on the basics of ALD growth are also included, reflecting a growing interest in precursor chemistry and growth

  2. Aerosol deposition on plant leaves

    Treesearch

    James B. Wedding; Roger W. Carlson; James J. Stukel; Fakhri A. Bazzaz

    1976-01-01

    An aerosol generator and wind tunnel system designed for use in aerosol deposition is described. Gross deposition on rough pubescent leaves was nearly 7 times greater than on smooth, waxy leaves. Results suggest that aerosol deposition, on a per unit area basis, for single horizontal streamlining leaves is similar to that for arrays of leaves under similar flow...

  3. Hydroquinone-ZnO nano-laminate deposited by molecular-atomic layer deposition

    NASA Astrophysics Data System (ADS)

    Huang, Jie; Lucero, Antonio T.; Cheng, Lanxia; Hwang, Hyeon Jun; Ha, Min-Woo; Kim, Jiyoung

    2015-03-01

    In this study, we have deposited organic-inorganic hybrid semiconducting hydroquinone (HQ)/zinc oxide (ZnO) superlattices using molecular-atomic layer deposition, which enables accurate control of film thickness, excellent uniformity, and sharp interfaces at a low deposition temperature (150 °C). Self-limiting growth of organic layers is observed for the HQ precursor on ZnO surface. Nano-laminates were prepared by varying the number of HQ to ZnO cycles in order to investigate the physical and electrical effects of different HQ to ZnO ratios. It is indicated that the addition of HQ layer results in enhanced mobility and reduced carrier concentration. The highest Hall mobility of approximately 2.3 cm2/V.s and the lowest n-type carrier concentration of approximately 1.0 × 1018/cm3 were achieved with the organic-inorganic superlattice deposited with a ratio of 10 ZnO cycles to 1 HQ cycle. This study offers an approach to tune the electrical transport characteristics of ALD ZnO matrix thin films using an organic dopant. Moreover, with organic embedment, this nano-laminate material may be useful for flexible electronics.

  4. Method for gas-metal arc deposition

    DOEpatents

    Buhrmaster, Carol L.; Clark, Denis E.; Smartt, Herschel B.

    1990-01-01

    Method and apparatus for gas-metal arc deposition of metal, metal alloys, and metal matrix composites. The apparatus contains an arc chamber for confining a D.C. electrical arc discharge, the arc chamber containing an outlet orifice in fluid communication with a deposition chamber having a deposition opening in alignment wiht the orifice for depositing metal droplets on a coatable substrate. Metal wire is passed continuously into the arc chamber in alignment with the orifice. Electric arcing between the metal wire anode and the orifice cathode produces droplets of molten metal from the wire which pass through the orifice and into the deposition chamber for coating a substrate exposed at the deposition opening. When producing metal matrix composites, a suspension of particulates in an inert gas enters the deposition chamber via a plurality of feed openings below and around the orifice so that reinforcing particulates join the metal droplets to produce a uniform mixture which then coats the exposed substrate with a uniform metal matrix composite.

  5. Apparatus for gas-metal arc deposition

    DOEpatents

    Buhrmaster, Carol L.; Clark, Denis E.; Smartt, Herschel B.

    1991-01-01

    Apparatus for gas-metal arc deposition of metal, metal alloys, and metal matrix composites. The apparatus contains an arc chamber for confining a D.C. electrical arc discharge, the arc chamber containing an outlet orifice in fluid communication with a deposition chamber having a deposition opening in alignment with the orifice for depositing metal droplets on a coatable substrate. Metal wire is passed continuously into the arc chamber in alignment with the orifice. Electric arcing between the metal wire anode and the orifice cathode produces droplets of molten metal from the wire which pass through the orifice and into the deposition chamber for coating a substrate exposed at the deposition opening. When producing metal matrix composites, a suspenion of particulates in an inert gas enters the deposition chamber via a plurality of feed openings below and around the orifice so that reinforcing particulates join the metal droplets to produce a uniform mixture which then coats the exposed substrate with a uniform metal matrix composite.

  6. 12 CFR 347.206 - Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 4 2011-01-01 2011-01-01 false Domestic retail deposit activity requiring... Banks § 347.206 Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank. (a) Domestic retail deposit activity. To initiate or conduct domestic retail deposit activity...

  7. 12 CFR 347.206 - Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 5 2014-01-01 2014-01-01 false Domestic retail deposit activity requiring... Banks § 347.206 Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank. (a) Domestic retail deposit activity. To initiate or conduct domestic retail deposit activity...

  8. 12 CFR 347.206 - Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 5 2013-01-01 2013-01-01 false Domestic retail deposit activity requiring... Banks § 347.206 Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank. (a) Domestic retail deposit activity. To initiate or conduct domestic retail deposit activity...

  9. 12 CFR 347.206 - Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 5 2012-01-01 2012-01-01 false Domestic retail deposit activity requiring... Banks § 347.206 Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank. (a) Domestic retail deposit activity. To initiate or conduct domestic retail deposit activity...

  10. 12 CFR 347.206 - Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 4 2010-01-01 2010-01-01 false Domestic retail deposit activity requiring... Banks § 347.206 Domestic retail deposit activity requiring deposit insurance by U.S. branch of a foreign bank. (a) Domestic retail deposit activity. To initiate or conduct domestic retail deposit activity...

  11. Ion beam sputter deposited diamond like films

    NASA Technical Reports Server (NTRS)

    Banks, B. A.; Rutledge, S. K.

    1982-01-01

    A single argon ion beam source was used to sputter deposit carbon films on fused silica, copper, and tantalum substrates under conditions of sputter deposition alone and sputter deposition combined with simultaneous argon ion bombardment. Simultaneously deposited and ion bombarded carbon films were prepared under conditions of carbon atom removal to arrival ratios of 0, 0.036, and 0.71. Deposition and etch rates were measured for films on fused silica substrates. Resulting characteristics of the deposited films are: electrical resistivity of densities of 2.1 gm/cu cm for sputter deposited films and 2.2 gm/cu cm for simultaneously sputter deposited and Ar ion bombarded films. For films approximately 1700 A thick deposited by either process and at 5550 A wavelength light the reflectance was 0.2, the absorptance was 0.7, the absorption coefficient was 67,000 cm to the -1 and the transmittance was 0.1.

  12. Giant landslide deposits in northwest Argentina

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

    Fauque, L.; Strecker, M.R.; Bloom, A.L.

    1985-01-01

    Giant Quaternary landslide deposits occur along mountain fronts in the structural transition zone between the high-angle reverse-fault-bounded Sierras Pampeanas and the low-angle thrust belt of the Sierras Subandinas. There are two modes of occurrence: (1) chaotic masses without distinct geometry, and (2) masses with distinct lobate geometry similar to glacial moraines. Type (1) deposits occur where the moving rock mass followed a narrow valley and blocked the drainage. Many of these caused subsequent formation of lakes and changed the sedimentation processes on pediments at the mountain fronts. In type (2) deposits, lateral and frontal ridges are up to 10 mmore » higher than the interior parts; in some places pressure ridges within the lobes are well preserved. Type (2) deposits show reverse grading and were deposited on relatively smooth pediments or alluvial fans. The lobate geometry strongly suggests that type (2) deposits are a product of flowage and are debris stream or sturzstrom deposits (sense of Heim, 1932 and Hsu, 1975). All investigated deposits occur in areas of demonstrated Quaternary faulting and are interpreted as the result of tectonic movements, although structural inhomogeneities in the source area may have been a significant factor for some of the landslides. No datable materials have yet been found associated with the deposits.« less

  13. Chemical vapor deposition growth

    NASA Technical Reports Server (NTRS)

    Ruth, R. P.; Manasevit, H. M.; Kenty, J. L.; Moudy, L. A.; Simpson, W. I.; Yang, J. J.

    1976-01-01

    A chemical vapor deposition (CVD) reactor system with a vertical deposition chamber was used for the growth of Si films on glass, glass-ceramic, and polycrystalline ceramic substrates. Silicon vapor was produced by pyrolysis of SiH4 in a H2 or He carrier gas. Preliminary deposition experiments with two of the available glasses were not encouraging. Moderately encouraging results, however, were obtained with fired polycrystalline alumina substrates, which were used for Si deposition at temperatures above 1,000 C. The surfaces of both the substrates and the films were characterized by X-ray diffraction, reflection electron diffraction, scanning electron microscopy optical microscopy, and surface profilometric techniques. Several experiments were conducted to establish baseline performance data for the reactor system, including temperature distributions on the sample pedestal, effects of carrier gas flow rate on temperature and film thickness, and Si film growth rate as a function of temperature.

  14. SAMPLE SIZE FOR SEASONAL MEAN CONCENTRATION, DEPOSITION VELOCITY AND DEPOSITION: A RESAMPLING STUDY

    EPA Science Inventory

    Methodologies are described to assign confidence statements to seasonal means of concentration (C), deposition velocity (V J, and deposition categorized by species/parameters, sites, and seasons in the presence of missing data. Estimators of seasonal means with missing weekly dat...

  15. A radon progeny deposition model

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

    Rielage, Keith; Elliott, Steven R; Hime, Andrew

    2010-12-01

    The next generation low-background detectors operating underground aim for unprecedented low levels of radioactive backgrounds. Although the radioactive decays of airborne radon (particularly {sup 222}Rn) and its subsequent progeny present in an experiment are potential backgrounds, also problematic is the deposition of radon progeny on detector materials. Exposure to radon at any stage of assembly of an experiment can result in surface contamination by progeny supported by the long half life (22 y) of {sup 210}Pb on sensitive locations of a detector. An understanding of the potential surface contamination from deposition will enable requirements of radon-reduced air and clean roommore » environments for the assembly of low background experiments. It is known that there are a number of environmental factors that govern the deposition of progeny onto surfaces. However, existing models have not explored the impact of some environmental factors important for low background experiments. A test stand has been constructed to deposit radon progeny on various surfaces under a controlled environment in order to develop a deposition model. Results from this test stand and the resulting deposition model are presented.« less

  16. Estimates of cloud water deposition at Mountain Acid Deposition Program sites in the Appalachian Mountains.

    PubMed

    Baumgardner, Ralph E; Isil, Selma S; Lavery, Thomas F; Rogers, Christopher M; Mohnen, Volker A

    2003-03-01

    Cloud water deposition was estimated at three high-elevation sites in the Appalachian Mountains of the eastern United States (Whiteface Mountain, NY; Whitetop Mountain, VA; and Clingman's Dome, TN) from 1994 through 1999 as part of the Mountain Acid Deposition Program (MADPro). This paper provides a summary of cloud water chemistry, cloud liquid water content, cloud frequency, estimates of cloud water deposition of sulfur and nitrogen species, and estimates of total deposition of sulfur and nitrogen at these sites. Other cloud studies in the Appalachians and their comparison to MADPro are also summarized. Whiteface Mountain exhibited the lowest mean and median concentrations of sulfur and nitrogen ions in cloud water, while Clingman's Dome exhibited the highest mean and median concentrations. This geographic gradient is partly an effect of the different meteorological conditions experienced at northern versus southern sites in addition to the difference in pollution content of air masses reaching the sites. All sites measured seasonal cloud water deposition rates of SO4(2-) greater than 50 kg/ha and NO3(-) rates of greater than 25 kg/ha. These high-elevation sites experienced additional deposition loading of SO4(2-) and NO3(-) on the order of 6-20 times greater compared with lower elevation Clean Air Status and Trends Network (CASTNet) sites. Approximately 80-90% of this extra loading is from cloud deposition.

  17. Electroless atomic layer deposition

    DOEpatents

    Robinson, David Bruce; Cappillino, Patrick J.; Sheridan, Leah B.; Stickney, John L.; Benson, David M.

    2017-10-31

    A method of electroless atomic layer deposition is described. The method electrolessly generates a layer of sacrificial material on a surface of a first material. The method adds doses of a solution of a second material to the substrate. The method performs a galvanic exchange reaction to oxidize away the layer of the sacrificial material and deposit a layer of the second material on the surface of the first material. The method can be repeated for a plurality of iterations in order to deposit a desired thickness of the second material on the surface of the first material.

  18. A suitable deposition method of CdS for high performance CdS-sensitized ZnO electrodes: Sequential chemical bath deposition

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

    Chen, Haining; Li, Weiping; Liu, Huicong

    2010-07-15

    A suitable deposition method of CdS is necessary for the high performance CdS-sensitized ZnO electrodes. In this paper, chemical bath deposition (CBD) and sequential chemical bath deposition (S-CBD) methods were used to deposit CdS on ZnO mesoporous films for ZnO/CdS electrodes. The analysis results of XRD patterns and UV-vis spectroscopy indicated that CBD deposition method leaded to the dissolving of ZnO mesoporous films in deposition solution and thickness reduction of ZnO/CdS electrodes. Absorption in visible region by the ZnO/CdS electrodes with CdS deposition by S-CBD was enhanced as deposition cycles increased due to the stability of ZnO mesoporous films inmore » the S-CBD deposition solutions. The results of photocurrent-voltage (I-V) measurement showed that the performance of ZnO/CdS electrodes with CdS deposition by CBD first increased and then decreased as deposition time increased, and the greatest short-circuit current (J{sub sc}) was obtained at the deposition time of 4 min. The performance of ZnO/CdS electrodes with CdS deposition by S-CBD increased as deposition cycles increased, and both open-circuit voltage (V{sub oc}) and J{sub sc} were greater than those electrodes with CdS deposition by CBD when the deposition cycles of S-CBD were 10 or greater. These results indicated that S-CBD is a more suitable method for high performance ZnO/CdS electrodes. (author)« less

  19. An upwelling model for the Phosphoria sea: A Permian, ocean-margin sea in the northwest United States

    USGS Publications Warehouse

    Piper, D.Z.; Link, P.K.

    2002-01-01

    The Permian Phosphoria Formation, a petroleum source rock and world-class phosphate deposit, was deposited in an epicratonic successor basin on the western margin of North America. We calculate the seawater circulation in the basin during deposition of the lower ore zone in the Meade Peak Member from the accumulation rates of carbonate fluorapatite and trace elements. The model gives the exchange rate of water between the Phosphoria sea and the open ocean to the west in terms of an upwelling rate (84 m yr-1) and residence time (4.2 yr) of seawater in the basin. These hydrographic properties supported a mean rate of primary productivity of 0.87 g m-2 d-1 of carbon in the uppermost few tens of meters of the water column (the photic zone) and denitrifying redox conditions in the bottom water (below approximately 150 m depth). High rain rates, onto the sea floor, of the organic matter that hosted the phosphate and several trace elements contributed to the accumulation of phosphorite, chert, and black shales and mudstones. Evaporation in the Goose Egg basin to the east of the Phosphoria basin ensured the import of surface seawater from the Phosphoria sea. Budgets of water, salt, phosphate, and oxygen, plus the minor accumulation of the biomarker gammacerane, show that exchange of water between the two basins was limited, possibly by the shallow carbonate platform that separated the two basins.

  20. Estimated variability of National Atmospheric Deposition Program/Mercury Deposition Network measurements using collocated samplers

    USGS Publications Warehouse

    Wetherbee, G.A.; Gay, D.A.; Brunette, R.C.; Sweet, C.W.

    2007-01-01

    The National Atmospheric Deposition Program/Mercury Deposition Network (MDN) provides long-term, quality-assured records of mercury in wet deposition in the USA and Canada. Interpretation of spatial and temporal trends in the MDN data requires quantification of the variability of the MDN measurements. Variability is quantified for MDN data from collocated samplers at MDN sites in two states, one in Illinois and one in Washington. Median absolute differences in the collocated sampler data for total mercury concentration are approximately 11% of the median mercury concentration for all valid 1999-2004 MDN data. Median absolute differences are between 3.0% and 14% of the median MDN value for collector catch (sample volume) and between 6.0% and 15% of the median MDN value for mercury wet deposition. The overall measurement errors are sufficiently low to resolve between NADP/MDN measurements by ??2 ng??l-1 and ??2 ????m-2?? year-1, which are the contour intervals used to display the data on NADP isopleths maps for concentration and deposition, respectively. ?? Springer Science+Business Media B.V. 2007.

  1. Deposition and clearance of inhaled particles.

    PubMed Central

    Stuart, B O

    1984-01-01

    Theoretical models of respiratory tract deposition of inhaled particles are compared to experimental studies of deposition patterns in humans and animals, as governed principally by particle size, density, respiratory rate and flow parameters. Various models of inhaled particle deposition make use of approximations of the respiratory tract to predict fractional deposition caused by fundamental physical processes of particle impaction, sedimentation, and diffusion. These models for both total deposition and regional (nasopharyngeal, tracheobronchial, and pulmonary) deposition are compared with early and recent experimental studies. Reasonable correlation has been obtained between theoretical and experimental studies, but the behavior in the respiratory tract of very fine (less than 0.1 micron) particles requires further investigation. Properties of particle shape, charge and hygroscopicity as well as the degree of respiratory tract pathology also influence deposition patterns; definitive experimental work is needed in these areas. The influence upon deposition patterns of dynamic alterations in inspiratory flow profiles caused by a variety of breathing patterns also requires further study, and the use of differing ventilation techniques with selected inhaled particle sizes holds promise in diagnosis of respiratory tract diseases. Mechanisms of conducting airway and alveolar clearance processes involving the pulmonary macrophage, mucociliary clearance, dissolution, transport to systemic circulation, and translocation via regional lymphatic vessels are discussed. PMID:6376108

  2. Method for gas-metal arc deposition

    DOEpatents

    Buhrmaster, C.L.; Clark, D.E.; Smartt, H.B.

    1990-11-13

    Method and apparatus for gas-metal arc deposition of metal, metal alloys, and metal matrix composites are disclosed. The apparatus contains an arc chamber for confining a D.C. electrical arc discharge, the arc chamber containing an outlet orifice in fluid communication with a deposition chamber having a deposition opening in alignment with the orifice for depositing metal droplets on a coatable substrate. Metal wire is passed continuously into the arc chamber in alignment with the orifice. Electric arcing between the metal wire anode and the orifice cathode produces droplets of molten metal from the wire which pass through the orifice and into the deposition chamber for coating a substrate exposed at the deposition opening. When producing metal matrix composites, a suspension of particulates in an inert gas enters the deposition chamber via a plurality of feed openings below and around the orifice so that reinforcing particulates join the metal droplets to produce a uniform mixture which then coats the exposed substrate with a uniform metal matrix composite. 1 fig.

  3. A new pulsed laser deposition technique: scanning multi-component pulsed laser deposition method.

    PubMed

    Fischer, D; de la Fuente, G F; Jansen, M

    2012-04-01

    The scanning multi-component pulsed laser deposition (PLD) method realizes uniform depositions of desired coatings by a modified pulsed laser deposition process, preferably with a femto-second laser-system. Multi-component coatings (single or multilayered) are thus deposited onto substrates via laser induced ablation of segmented targets. This is achieved via horizontal line-scanning of a focused laser beam over a uniformly moving target's surface. This process allows to deposit the desired composition of the coating simultaneously, starting from the different segments of the target and adjusting the scan line as a function of target geometry. The sequence and thickness of multilayers can easily be adjusted by target architecture and motion, enabling inter/intra layer concentration gradients and thus functional gradient coatings. This new, simple PLD method enables the achievement of uniform, large-area coatings. Case studies were performed with segmented targets containing aluminum, titanium, and niobium. Under the laser irradiation conditions applied, all three metals were uniformly ablated. The elemental composition within the rough coatings obtained was fixed by the scanned area to Ti-Al-Nb = 1:1:1. Crystalline aluminum, titanium, and niobium were found to coexist side by side at room temperature within the substrate, without alloy formation up to 600 °C. © 2012 American Institute of Physics

  4. Nickel-cobalt laterites: a deposit model: Chapter H in Mineral deposit models for resource assessment

    USGS Publications Warehouse

    Marsh, Erin; Anderson, Eric J.; Gray, Floyd

    2013-01-01

    Nickel-cobalt (Ni-Co) laterite deposits are supergene enrichments of Ni±Co that form from intense chemical and mechanical weathering of ultramafic parent rocks. These regolith deposits typically form within 26 degrees of the equator, although there are a few exceptions. They form in active continental margins and stable cratonic settings. It takes as little as one million years for a laterite profile to develop. Three subtypes of Ni-Co laterite deposits are classified according to the dominant Ni-bearing mineralogy, which include hydrous magnesium (Mg)-silicate, smectite, and oxide. These minerals form in weathering horizons that begin with the unweathered protolith at the base, saprolite next, a smectite transition zone only in profiles where drainage is very poor, followed by limonite, and then capped with ferricrete at the top. The saprolite contains Ni-rich hydrous Mg-silicates, the Ni-rich clays occur in the transition horizon, and Ni-rich goethite occurs in the limonite. Although these subtypes of deposits are the more widely used terms for classification of Ni-Co laterite deposits, most deposits have economic concentrations of Ni in more than one horizon. Because of their complex mineralogy and heterogeneous concentrations, mining of these metallurgically complex deposits can be challenging. Deposits range in size from 2.5 to about 400 million tonnes, with Ni and Co grades of 0.66–2.4 percent (median 1.3) and 0.01–0.15 percent (median 0.08), respectively. Modern techniques of ore delineation and mineralogical identification are being developed to aid in streamlining the Ni-Co laterite mining process, and low-temperature and low-pressure ore processing techniques are being tested that will treat the entire weathered profile. There is evidence that the production of Ni and Co from laterites is more energy intensive than that of sulfide ores, reflecting the environmental impact of producing a Ni-Co laterite deposit. Tailings may include high levels of

  5. Copper Deposits in Sedimentary and Volcanogenic Rocks

    USGS Publications Warehouse

    Tourtelot, Elizabeth B.; Vine, James David

    1976-01-01

    Copper deposits occur in sedimentary and volcanogenic rocks within a wide variety of geologic environments where there may be little or no evidence of hydrothermal alteration. Some deposits may be hypogene and have a deep-seated source for the ore fluids, but because of rapid cooling and dilution during syngenetic deposition on the ocean floor, the resulting deposits are not associated with hydrothermal alteration. Many of these deposits are formed at or near major tectonic features on the Earth's crust, including plate boundaries, rift valleys, and island arcs. The resulting ore bodies may be stratabound and either massive or disseminated. Other deposits form in rocks deposited in shallow-marine, deltaic, and nonmarine environments by the movement and reaction of interstratal brines whose metal content is derived from buried sedimentary and volcanic rocks. Some of the world's largest copper deposits were probably formed in this manner. This process we regard as diagenetic, but some would regard it as syngenetic, if the ore metals are derived from disseminated metal in the host-rock sequence, and others would regard the process as epigenetic, if there is demonstrable evidence of ore cutting across bedding. Because the oxidation associated with diagenetic red beds releases copper to ground-water solutions, red rocks and copper deposits are commonly associated. However, the ultimate size, shape, and mineral zoning of a deposit result from local conditions at the site of deposition - a logjam in fluvial channel sandstone may result in an irregular tabular body of limited size; a petroleum-water interface in an oil pool may result in a copper deposit limited by the size and shape of the petroleum reservoir; a persistent thin bed of black shale may result in a copper deposit the size and shape of that single bed. The process of supergene enrichment has been largely overlooked in descriptions of copper deposits in sedimentary rocks. However, supergene processes may be

  6. Possible Roles of Fluoride and Carbonate in Biochemical Carbonated Apatite Formation

    NASA Astrophysics Data System (ADS)

    Meouch, Orysia; Omelon, Sidney

    2016-04-01

    Marine phosphorites are predominantly composed of carbonated fluorapatite (CFA = Ca10-a-b-cNaaMgb(PO4)6-x(CO3)x-y-z(CO3.F)y(SO4)zF2, where x=y+a+2c, and c represents the number of Ca vacancies, with a P2O5 content that ranges from 18-40 %. Sulphur-oxidizing bacteria of the Beggiatoa genus concentration phosphorous as intracellular polyphosphate ((PO3-)n) which is depolymerized into inorganic orthophosphate (Pi). Consequently, an increase in pore water Pi concentration favours carbonated apatite precipitation. The carbonate and fluoride that is characteristic of phosphorite CFA is also located in the vertebrate skeleton. This similarity suggests a biochemical pathway for CFA precipitation. Preliminary Raman spectroscopy and powder x-ray diffraction results that suggest a role for fluoride, and possibly carbonate, in the biochemical depolymerisation of polyphosphates with alkaline phosphatase will be presented.

  7. Particle formation in SiOx film deposition by low frequency plasma enhanced chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Yamaguchi, Tomoyo; Sakamoto, Naoshi; Shimozuma, Mitsuo; Yoshino, Masaki; Tagashira, Hiroaki

    1998-01-01

    Dust particle formation dynamics in the process of SiOx film deposition from a SiH4 and N2O gas mixture by a low frequency plasma enhanced chemical vapor deposition have been investigated using scanning electron microscopy and laser light scattering. The deposited films are confirmed to be SiOx from the measurements of Auger electron spectroscopy, x-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy. It is observed by scanning electron microscopy that particles are deposited on Si substrate at the plasma power frequency f=5 kHz and above both with and without substrate heating (400 °C), while no particle is deposited below f=1 kHz. Moreover, the laser light scattering indicates that particles are generated at the plasma power frequency of f=3 kHz and above in the gas phase, and that they are not generated in the gas phase at below f=3 kHz. Properties (the refractive index, resistivity, and Vickers hardness) of the films with particles are inferior to those of the films without particles. This article has revealed experimentally the effect of plasma power frequency on SiOx particle formation and makes a contribution to the explication of the particle formation mechanism. We suggest that high-quality film deposition with the low frequency plasma enhanced chemical vapor deposition method is attained at f=1 kHz or less without substrate heating.

  8. 12 CFR 347.203 - Deposit insurance required for all branches of foreign banks engaged in domestic retail deposit...

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... foreign banks engaged in domestic retail deposit activity in the same State. 347.203 Section 347.203 Banks... engaged in domestic retail deposit activity in the same State. The FDIC will not insure deposits in any... foreign bank in the same state that engages in domestic retail deposit activity will be an insured branch. ...

  9. 12 CFR 347.203 - Deposit insurance required for all branches of foreign banks engaged in domestic retail deposit...

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... foreign banks engaged in domestic retail deposit activity in the same State. 347.203 Section 347.203 Banks... engaged in domestic retail deposit activity in the same State. The FDIC will not insure deposits in any... foreign bank in the same state that engages in domestic retail deposit activity will be an insured branch. ...

  10. 12 CFR 347.203 - Deposit insurance required for all branches of foreign banks engaged in domestic retail deposit...

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... foreign banks engaged in domestic retail deposit activity in the same State. 347.203 Section 347.203 Banks... engaged in domestic retail deposit activity in the same State. The FDIC will not insure deposits in any... foreign bank in the same state that engages in domestic retail deposit activity will be an insured branch. ...

  11. 12 CFR 347.203 - Deposit insurance required for all branches of foreign banks engaged in domestic retail deposit...

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... foreign banks engaged in domestic retail deposit activity in the same State. 347.203 Section 347.203 Banks... engaged in domestic retail deposit activity in the same State. The FDIC will not insure deposits in any... foreign bank in the same state that engages in domestic retail deposit activity will be an insured branch. ...

  12. 12 CFR 347.203 - Deposit insurance required for all branches of foreign banks engaged in domestic retail deposit...

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... foreign banks engaged in domestic retail deposit activity in the same State. 347.203 Section 347.203 Banks... engaged in domestic retail deposit activity in the same State. The FDIC will not insure deposits in any... foreign bank in the same state that engages in domestic retail deposit activity will be an insured branch. ...

  13. Stratigraphy of Upper Cretaceous and Cenozoic deposits of the Bakchar iron ore deposit (southwestern Siberia): New data

    NASA Astrophysics Data System (ADS)

    Lebedeva, N. K.; Kuzmina, O. B.; Sobolev, E. S.; Khazina, I. V.

    2017-01-01

    The results of complex palynological and microfaunistic studies of Upper Cretaceous and Cenozoic deposits of the Bakchar iron ore deposit are presented. Geochronologically, the age of the deposits varies from Campanian to Quaternary. It was established that the Slavgorod, Gan'kino, and Jurki (?) formations contain four biostratons in the rank of beds with dinocysts and three biostratons in the rank of beds with spores and pollen. The Cenozoic continental deposits contain four biostratons in the rank of beds, containing spores and pollen. As a result of the study, a large stratigraphic gap in the Cretaceous-Paleogene boundary deposits, covering a significant part of the Maastrichtian, Paleocene, Ypresian, and Lutetian stages of the Eocene, was established. The remnants of a new morphotype of heteromorphic ammonites of genus Baculites were first described in deposits of the Slavgorod Formation (preliminarily, upper Campanian). The distribution features of the different palynomorph groups in the Upper Cretaceous-Cenozoic deposits in the area of study due to transgressive-regressive cycles and climate fluctuations were revealed.

  14. Descriptive and geoenvironmental model for Co-Cu-Au deposits in metasedimentary rocks: Chapter G in Mineral deposit models for resource assessment

    USGS Publications Warehouse

    Slack, John F.; Johnson, Craig A.; Causey, J. Douglas; Lund, Karen; Schulz, Klaus J.; Gray, John E.; Eppinger, Robert G.; Slack, John F.

    2013-01-01

    Additional geologically and compositionally similar deposits are known, but have average Co grades less than 0.1 percent. Most of these deposits contain cobalt-rich pyrite and lack appreciable amounts of distinct Co sulfide and (or) sulfarsenide minerals. Such deposits are not discussed in detail in the following sections, but these deposits may be revelant to the descriptive and genetic models presented below. Examples include the Scadding Au-Co-Cu deposit in Ontario, Canada; the Vähäjoki Co-Cu-Au deposit in Finland; the Tuolugou Co-Au deposit in Qinghai Province, China; the Lala Co-Cu-UREE deposit in Sichuan Province, China; the Guelb Moghrein Cu-Au-Co deposit in Mauritania; and the Great Australia Co-Cu, Greenmount Cu-Au-Co, and Monakoff Cu-Au-Co-UAg deposits in Queensland, Australia. Detailed information on these deposits is presented in appendix 2.

  15. Sinks for inorganic nitrogen deposition in forest ecosystems with low and high nitrogen deposition in China.

    PubMed

    Sheng, Wenping; Yu, Guirui; Fang, Huajun; Jiang, Chunming; Yan, Junhua; Zhou, Mei

    2014-01-01

    We added the stable isotope (15)N in the form of ((15)NH4)2SO4 and K(15)NO3 to forest ecosystems in eastern China under two different N deposition levels to study the fate of the different forms of deposited N. Prior to the addition of the (15)N tracers, the natural (15)N abundance ranging from -3.4‰ to +10.9‰ in the forest under heavy N deposition at Dinghushan (DHS), and from -3.92‰ to +7.25‰ in the forest under light N deposition at Daxinganling (DXAL). Four months after the tracer application, the total (15)N recovery from the major ecosystem compartments ranged from 55.3% to 90.5%. The total (15)N recoveries were similar under the ((15)NH4)2SO4 tracer treatment in both two forest ecosystems, whereas the total (15)N recovery was significantly lower in the subtropical forest ecosystem at DHS than in the boreal forest ecosystem at DXAL under the K(15)NO3 tracer treatment. The (15)N assimilated into the tree biomass represented only 8.8% to 33.7% of the (15)N added to the forest ecosystems. In both of the tracer application treatments, more (15)N was recovered from the tree biomass in the subtropical forest ecosystem at DHS than the boreal forest ecosystem at DXAL. The amount of (15)N assimilated into tree biomass was greater under the K(15)NO3 tracer treatment than that of the ((15)NH4)2SO4 treatment in both forest ecosystems. This study suggests that, although less N was immobilized in the forest ecosystems under more intensive N deposition conditions, forest ecosystems in China strongly retain N deposition, even in areas under heavy N deposition intensity or in ecosystems undergoing spring freezing and thawing melts. Compared to ammonium deposition, deposited nitrate is released from the forest ecosystem more easily. However, nitrate deposition could be retained mostly in the plant N pool, which might lead to more C sequestration in these ecosystems.

  16. Dry deposition fluxes and deposition velocities of trace metals in the Tokyo metropolitan area measured with a water surface sampler.

    PubMed

    Sakata, Masahiro; Marumoto, Kohji

    2004-04-01

    Dry deposition fluxes and deposition velocities (=deposition flux/atmospheric concentration) for trace metals including Hg, Cd, Cu, Mn, Pb, and Zn in the Tokyo metropolitan area were measured using an improved water surface sampler. Mercury is deposited on the water surface in both gaseous (reactive gaseous mercury, RGM) and particulate (particulate mercury, Hg(p)) forms. The results based on 1 yr observations found that dry deposition plays a significant if not dominant role in trace metal deposition in this urban area, contributing fluxes ranging from 0.46 (Cd) to 3.0 (Zn) times those of concurrent wet deposition fluxes. The deposition velocities were found to be dependent on the deposition of coarse particles larger than approximately 5 microm in diameter on the basis of model calculations. Our analysis suggests that the 84.13% diameter is a more appropriate index for each deposited metal than the 50% diameter in the assumed undersize log-normal distribution, because larger particles are responsible for the flux. The deposition velocities for trace metals other than mercury increased exponentially with an increase in their 84.13% diameters. Using this regression equation, the deposition velocities for Hg(p) were estimated from its 84.13% diameter. The deposition fluxes for Hg(p) calculated from the estimated velocities tended to be close to the mercury fluxes measured with the water surface sampler during the study periods except during summer.

  17. Preliminary Model of Porphyry Copper Deposits

    USGS Publications Warehouse

    Berger, Byron R.; Ayuso, Robert A.; Wynn, Jeffrey C.; Seal, Robert R.

    2008-01-01

    The U.S. Geological Survey (USGS) Mineral Resources Program develops mineral-deposit models for application in USGS mineral-resource assessments and other mineral resource-related activities within the USGS as well as for nongovernmental applications. Periodic updates of models are published in order to incorporate new concepts and findings on the occurrence, nature, and origin of specific mineral deposit types. This update is a preliminary model of porphyry copper deposits that begins an update process of porphyry copper models published in USGS Bulletin 1693 in 1986. This update includes a greater variety of deposit attributes than were included in the 1986 model as well as more information about each attribute. It also includes an expanded discussion of geophysical and remote sensing attributes and tools useful in resource evaluations, a summary of current theoretical concepts of porphyry copper deposit genesis, and a summary of the environmental attributes of unmined and mined deposits.

  18. Wet Dust Deposition Across Texas, USA

    NASA Astrophysics Data System (ADS)

    Collins, J. D., Jr.; Ponette-González, A.; Gill, T. E.; Glass, G. A.; Weathers, K. C.

    2016-12-01

    Atmospheric dust deposition is of critical importance in terrestrial biogeochemical cycles, supplying essential limiting nutrients, such as calcium and phosphorus as well as pollutants, such as lead, to ecosystems. Dust particles are delivered to terrestrial ecosystems directly as dry deposition or in precipitation (wet deposition) as a result of rainout (particles incorporated into cloud droplets) and washout (particles that collide with raindrops as they fall). Compared to dry deposition, wet dust deposition (dissolved + particulate) is a poorly understood yet potentially significant pathway for dust input, especially in humid regions. We quantified wet dust deposition to two National Atmospheric Deposition Monitoring (NADP) sites across Texas-one in west (Guadalupe Mountains) and one in east (near Houston) Texas-with contrasting climate/dust regimes and land cover. We focused on 2012 during one of the most severe droughts in Texas since 1895. Dust event days (DEDs) were identified using meteorological data for stations within 150 km of the NADP sites where wet deposition was sampled weekly. DEDs were defined using the following criteria: visibility <10 km, <30% relative humidity, and wind speed >50 km, supplemented with other Saharan dust incursion and dust observations. A total of 34 DEDs (20 sample weeks) were identified for the west and 5 DEDs (4 sample weeks) for the east Texas sites. Bulk elemental composition of washout particles is analyzed using Particle Induced X-ray Emission (PIXE) spectroscopy and X-ray Fluorescence (XRF) spectroscopy. Using these data, we will examine differences in the chemical composition of rainwater and aerosol particles filtered from rain samples for dust versus non-dust event days at each study site. Deposition fluxes for dust and non-dust event weeks are also compared. Quantifying the magnitude of wet dust deposition is necessary to improve evaluation of dust impacts on biogeochemical cycles.

  19. 17 CFR 10.44 - Depositions and interrogatories.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 17 Commodity and Securities Exchanges 1 2011-04-01 2011-04-01 false Depositions and... OF PRACTICE Prehearing Procedures; Prehearing Conferences; Discovery; Depositions § 10.44 Depositions... that the absence of the witness was procured by the party seeking to take the deposition), (2) His...

  20. 17 CFR 10.44 - Depositions and interrogatories.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 17 Commodity and Securities Exchanges 1 2010-04-01 2010-04-01 false Depositions and... OF PRACTICE Prehearing Procedures; Prehearing Conferences; Discovery; Depositions § 10.44 Depositions... that the absence of the witness was procured by the party seeking to take the deposition), (2) His...

  1. Chemical vapor deposition of epitaxial silicon

    DOEpatents

    Berkman, Samuel

    1984-01-01

    A single chamber continuous chemical vapor deposition (CVD) reactor is described for depositing continuously on flat substrates, for example, epitaxial layers of semiconductor materials. The single chamber reactor is formed into three separate zones by baffles or tubes carrying chemical source material and a carrier gas in one gas stream and hydrogen gas in the other stream without interaction while the wafers are heated to deposition temperature. Diffusion of the two gas streams on heated wafers effects the epitaxial deposition in the intermediate zone and the wafers are cooled in the final zone by coolant gases. A CVD reactor for batch processing is also described embodying the deposition principles of the continuous reactor.

  2. STRONTIUM 90: ESTIMATION OF WORLDWIDE DEPOSITION.

    PubMed

    VOLCHOK, H L

    1964-09-25

    The relation between the worldwide deposition of strontium-90, as calculated by many investigators over the last decade, and that observed in rainfall in New York City has been relatively constant. On the average, for each millicurie of strontium-90 per square mile deposited in New York City, 0.055 megacurie has been deposited on the earth's total surface. Cumulative deposits of strontium-90 on the earth's surface at various intervals over the last 10 years have been computed from this ratio. From the mean quarterly fraction of the annual strontium-90 fallout in New York City for the last 9 years, the worldwide deposition of this nuclide, equal to 2.48 megacuries, is predicted for 1964.

  3. Diverse Deposits in Melas Chasma

    NASA Image and Video Library

    2015-07-29

    This scene captured by NASA Mars Reconnaissance Orbiter includes chaotic deposits with a wide range of colors. The deposits are distinctive with both unique colors and small-scale textures such as fracture patterns. These are probably sedimentary rocks, transported and deposited in water or air. The original layers may have been jumbled in a landslide. Dark or reddish sand dunes cover some of the bedrock. http://photojournal.jpl.nasa.gov/catalog/PIA19860

  4. 5 CFR 1201.75 - Taking depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 5 Administrative Personnel 3 2011-01-01 2011-01-01 false Taking depositions. 1201.75 Section 1201.75 Administrative Personnel MERIT SYSTEMS PROTECTION BOARD ORGANIZATION AND PROCEDURES PRACTICES AND PROCEDURES Procedures for Appellate Cases Discovery § 1201.75 Taking depositions. Depositions may be taken by...

  5. 38 CFR 18b.55 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 38 Pensions, Bonuses, and Veterans' Relief 2 2010-07-01 2010-07-01 false Depositions. 18b.55... Procedures § 18b.55 Depositions. Upon such terms as may be just, for the convenience of the parties or of the... be taken by deposition. ...

  6. 38 CFR 18b.55 - Depositions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 38 Pensions, Bonuses, and Veterans' Relief 2 2011-07-01 2011-07-01 false Depositions. 18b.55... Procedures § 18b.55 Depositions. Upon such terms as may be just, for the convenience of the parties or of the... be taken by deposition. ...

  7. 5 CFR 1201.75 - Taking depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 5 Administrative Personnel 3 2010-01-01 2010-01-01 false Taking depositions. 1201.75 Section 1201.75 Administrative Personnel MERIT SYSTEMS PROTECTION BOARD ORGANIZATION AND PROCEDURES PRACTICES AND PROCEDURES Procedures for Appellate Cases Discovery § 1201.75 Taking depositions. Depositions may be taken by...

  8. 48 CFR 6101.15 - Depositions [Rule 15].

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 48 Federal Acquisition Regulations System 7 2010-10-01 2010-10-01 false Depositions [Rule 15..., GENERAL SERVICES ADMINISTRATION CONTRACT DISPUTE CASES 6101.15 Depositions [Rule 15]. (a) When depositions... deposition upon oral examination or written questions before an officer authorized to administer oaths at the...

  9. 48 CFR 6101.15 - Depositions [Rule 15].

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 48 Federal Acquisition Regulations System 7 2011-10-01 2011-10-01 false Depositions [Rule 15..., GENERAL SERVICES ADMINISTRATION CONTRACT DISPUTE CASES 6101.15 Depositions [Rule 15]. (a) When depositions... deposition upon oral examination or written questions before an officer authorized to administer oaths at the...

  10. Sediment-hosted Pb-Zn Deposits: a global perspective

    USGS Publications Warehouse

    Leach, David L.; Sangster, Donald F.; Kelley, Karen D.; Large, R; Garven, G.; Allen, Craig R.

    2005-01-01

    Sediment-hosted Pb-Zn deposits contain the world's greatest lead and zinc resources and dominate world production of these metals. They are a chverse group of ore deposits hosted by a wide variety of carbonate and siliciclastic roch that have no obviolls genetic association with igneous activity. A nmge of ore-fortl1ing processes in a vmiety of geologic and tectonic environments created these deposits over at least two billion years of Earth history. The metals were precipitated by basinal brines in synsedimentary and early diagenetic to low-grade metamorphic environments. The deposits display a broad range of relationships to enclosing host rocks that includes stratiform, strata-bound, and discordant ores. These ores are divided into two broad subt)1Jes: Mississippi Valley-type (MVT) and sedimentmy exhalative (SEDEX), Despite the "exhalative" component inherent in the term "SEDEX," in this manusclipt, direct evidence of an exhalite in the ore or alteration component is not essential for a deposit to be classified as SEDEX. The presence of laminated sulfides parallel to bedding is assumed to be permissive evidence for exhalative ores. The chstinction between some SEDEX and MVT depOSits can be quite subjective because some SEDEX ores replaced carbonate, whereas some MVT depOSits formed in an early diagenetic environment and display laminated ore textures. Geologic and resource information are presented for 248 depositS that provide a framework to describe ,mel compare these deposits. Nine of tlle 10 largest sediment-hosted Pb-Zn deposits are SEDEX, Of the deposits that contain at least 2.5 million metric tons (Mt), there are 35 SEDEX (excluding Broken Hill-type) deposits and 15 MVT (excluding Iris-type) deposits. Despite the skewed distribution of the deposit size, the two deposits types have an excellent correlation between total tonnage and tonnage of contained metal (Pb + Zn), with a fairly consistent ratio of about lO/l, regardless of the size of the deposit or

  11. 47 CFR 32.4040 - Customers' deposits.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 47 Telecommunication 2 2010-10-01 2010-10-01 false Customers' deposits. 32.4040 Section 32.4040... FOR TELECOMMUNICATIONS COMPANIES Instructions for Balance Sheet Accounts § 32.4040 Customers' deposits. (a) This account shall include the amount of cash deposited with the company by customers as security...

  12. 24 CFR 891.775 - Security deposits.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 24 Housing and Urban Development 4 2013-04-01 2013-04-01 false Security deposits. 891.775 Section 891.775 Housing and Urban Development REGULATIONS RELATING TO HOUSING AND URBAN DEVELOPMENT (CONTINUED... Individuals-Section 162 Assistance § 891.775 Security deposits. The general requirements for security deposits...

  13. 24 CFR 891.775 - Security deposits.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 24 Housing and Urban Development 4 2010-04-01 2010-04-01 false Security deposits. 891.775 Section 891.775 Housing and Urban Development Regulations Relating to Housing and Urban Development (Continued... Individuals-Section 162 Assistance § 891.775 Security deposits. The general requirements for security deposits...

  14. Hydrodynamic and Chemical Modeling of a Chemical Vapor Deposition Reactor for Zirconia Deposition

    NASA Astrophysics Data System (ADS)

    Belmonte, T.; Gavillet, J.; Czerwiec, T.; Ablitzer, D.; Michel, H.

    1997-09-01

    Zirconia is deposited on cylindrical substrates by flowing post-discharge enhanced chemical vapor deposition. In this paper, a two dimensional hydrodynamic and chemical modeling of the reactor is described for given plasma characteristics. It helps in determining rate constants of the synthesis reaction of zirconia in gas phase and on the substrate which is ZrCl4 hydrolysis. Calculated deposition rate profiles are obtained by modeling under various conditions and fits with a satisfying accuracy the experimental results. The role of transport processes and the mixing conditions of excited gases with remaining ones are studied. Gas phase reaction influence on the growth rate is also discussed.

  15. Water evaporation in silica colloidal deposits.

    PubMed

    Peixinho, Jorge; Lefèvre, Grégory; Coudert, François-Xavier; Hurisse, Olivier

    2013-10-15

    The results of an experimental study on the evaporation and boiling of water confined in the pores of deposits made of mono-dispersed silica colloidal micro-spheres are reported. The deposits are studied using scanning electron microscopy, adsorption of nitrogen, and adsorption of water through attenuated total reflection-infrared spectroscopy. The evaporation is characterized using differential scanning calorimetry and thermal gravimetric analysis. Optical microscopy is used to observe the patterns on the deposits after evaporation. When heating at a constant rate and above boiling temperature, the release of water out of the deposits is a two step process. The first step is due to the evaporation and boiling of the surrounding and bulk water and the second is due to the desorption of water from the pores. Additional experiments on the evaporation of water from membranes having cylindrical pores and of heptane from silica deposits suggest that the second step is due to the morphology of the deposits. Copyright © 2013 Elsevier Inc. All rights reserved.

  16. Dry deposition models for radionuclides dispersed in air: a new approach for deposition velocity evaluation schema

    NASA Astrophysics Data System (ADS)

    Giardina, M.; Buffa, P.; Cervone, A.; De Rosa, F.; Lombardo, C.; Casamirra, M.

    2017-11-01

    In the framework of a National Research Program funded by the Italian Minister of Economic Development, the Department of Energy, Information Engineering and Mathematical Models (DEIM) of Palermo University and ENEA Research Centre of Bologna, Italy are performing several research activities to study physical models and mathematical approaches aimed at investigating dry deposition mechanisms of radioactive pollutants. On the basis of such studies, a new approach to evaluate the dry deposition velocity for particles is proposed. Comparisons with some literature experimental data show that the proposed dry deposition scheme can capture the main phenomena involved in the dry deposition process successfully.

  17. Salicylic acid deposition from wash-off products: comparison of in vivo and porcine deposition models.

    PubMed

    Davies, M A

    2015-10-01

    Salicylic acid (SA) is a widely used active in anti-acne face wash products. Only about 1-2% of the total dose is actually deposited on skin during washing, and more efficient deposition systems are sought. The objective of this work was to develop an improved method, including data analysis, to measure deposition of SA from wash-off formulae. Full fluorescence excitation-emission matrices (EEMs) were acquired for non-invasive measurement of deposition of SA from wash-off products. Multivariate data analysis methods - parallel factor analysis and N-way partial least-squares regression - were used to develop and compare deposition models on human volunteers and porcine skin. Although both models are useful, there are differences between them. First, the range of linear response to dosages of SA was 60 μg cm(-2) in vivo compared to 25 μg cm(-2) on porcine skin. Second, the actual shape of the SA band was different between substrates. The methods employed in this work highlight the utility of the use of EEMs, in conjunction with multivariate analysis tools such as parallel factor analysis and multiway partial least-squares calibration, in determining sources of spectral variability in skin and quantification of exogenous species deposited on skin. The human model exhibited the widest range of linearity, but porcine model is still useful up to deposition levels of 25 μg cm(-2) or used with nonlinear calibration models. © 2015 Society of Cosmetic Scientists and the Société Française de Cosmétologie.

  18. 20 CFR 725.458 - Depositions; interrogatories.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 20 Employees' Benefits 3 2010-04-01 2010-04-01 false Depositions; interrogatories. 725.458 Section... MINE SAFETY AND HEALTH ACT, AS AMENDED Hearings § 725.458 Depositions; interrogatories. The testimony of any witness or party may be taken by deposition or interrogatory according to the rules of...

  19. 20 CFR 725.458 - Depositions; interrogatories.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 20 Employees' Benefits 3 2011-04-01 2011-04-01 false Depositions; interrogatories. 725.458 Section... FEDERAL MINE SAFETY AND HEALTH ACT, AS AMENDED Hearings § 725.458 Depositions; interrogatories. The testimony of any witness or party may be taken by deposition or interrogatory according to the rules of...

  20. 49 CFR 1114.24 - Depositions; procedures.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 8 2010-10-01 2010-10-01 false Depositions; procedures. 1114.24 Section 1114.24... OF TRANSPORTATION RULES OF PRACTICE EVIDENCE; DISCOVERY Discovery § 1114.24 Depositions; procedures... objections made at the time of the examination to the qualifications of the officer taking the deposition, or...

  1. 43 CFR 4.115 - Discovery-depositions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false Discovery-depositions. 4.115 Section 4.115... Discovery—depositions. (a) General policy and protective orders. The parties are encouraged to engage in voluntary discovery procedures. In connection with any deposition or other discovery procedure, the board...

  2. 49 CFR 1114.24 - Depositions; procedures.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 8 2011-10-01 2011-10-01 false Depositions; procedures. 1114.24 Section 1114.24... OF TRANSPORTATION RULES OF PRACTICE EVIDENCE; DISCOVERY Discovery § 1114.24 Depositions; procedures... objections made at the time of the examination to the qualifications of the officer taking the deposition, or...

  3. 22 CFR 92.64 - Filing depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 22 Foreign Relations 1 2010-04-01 2010-04-01 false Filing depositions. 92.64 Section 92.64 Foreign Relations DEPARTMENT OF STATE LEGAL AND RELATED SERVICES NOTARIAL AND RELATED SERVICES Depositions and Letters Rogatory § 92.64 Filing depositions. (a) Preparation and transmission of envelope. The notice or...

  4. 22 CFR 92.64 - Filing depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 22 Foreign Relations 1 2011-04-01 2011-04-01 false Filing depositions. 92.64 Section 92.64 Foreign Relations DEPARTMENT OF STATE LEGAL AND RELATED SERVICES NOTARIAL AND RELATED SERVICES Depositions and Letters Rogatory § 92.64 Filing depositions. (a) Preparation and transmission of envelope. The notice or...

  5. 12 CFR 19.170 - Discovery depositions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 1 2012-01-01 2012-01-01 false Discovery depositions. 19.170 Section 19.170 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY RULES OF PRACTICE AND PROCEDURE Discovery Depositions and Subpoenas § 19.170 Discovery depositions. (a) General rule. In any...

  6. Deposition of ozone to tundra

    NASA Technical Reports Server (NTRS)

    Jacob, D. J.; Fan, S.-M.; Wofsy, S. C.; Spiro, P. A.; Bakwin, P. S.; Ritter, J. A.; Browell, E. V.; Gregory, G. L.; Fitzjarrald, D. R.; Moore, K. E.

    1992-01-01

    Eddy correlation measurements of O3 deposition fluxes to tundra during the Arctic Boundary Layer Expedition (ABLE 3A) are reported. The mean O3 deposition velocity was 0.24 cm/s in the daytime and 0.12 cm/s at night. The day-to-day difference in deposition velocity was driven by both atmospheric stability and surface reactivity. The mean surface resistance to O3 deposition was 2.6 s/cm in the daytime and 3.4 s/cm at night. The relatively low surface resistance at night is attributed to light-insensitive uptake of O3 at dry upland tundra surfaces. The small day-tonight difference in surface resistance is attributed to additional stomatal uptake by wet meadow tundra plants in the daytime. The mean O3 deposition flux to the world north of 60 deg N in July-August is estimated at 8.2 x 10 exp 10 molecules/sq cm/s. Suppression of photochemical loss by small anthropogenic inputs of nitrogen oxides could have a major effect on O3 concentrations in the summertime Arctic troposphere.

  7. Venus - Landslide Deposits

    NASA Technical Reports Server (NTRS)

    1992-01-01

    The Magellan spacecraft has observed remnant landslide deposits apparently resulting from the collapse of volcanic structures. This image, centered at 45.2 degrees south latitude, 201.4 degrees east longitude, shows a collapse deposit 70 kilometers (43 miles) across. The bright, highly textured deposit near the center of the image probably consists of huge blocks of fractured volcanic rock, many as large as several hundred meters across. A remnant of the volcano itself, about 20 kilometers (12.4 miles) across, is seen at the center of the image. The distorted radar appearance of the volcano is a result of extremely steep slopes on the 'scars' from which the landslide material originated. A field of numerous small volcanic domes can be seen in the northern half of the image. The bright irregular lineaments trending to the north-northwest are ridges caused by regional tectonic deformation of the upper layers of the Venusian crust.

  8. Depositional processes in large-scale debris-flow experiments

    USGS Publications Warehouse

    Major, J.J.

    1997-01-01

    This study examines the depositional process and characteristics of deposits of large-scale experimental debris flows (to 15 m3) composed of mixtures of gravel (to 32 mm), sand, and mud. The experiments were performed using a 95-m-long, 2-m-wide debris-flow flume that slopes 31??. Following release, experimental debris flows invariably developed numerous shallow (???10 cm deep) surges. Sediment transported by surges accumulated abruptly on a 3?? runout slope at the mouth of the flume. Deposits developed in a complex manner through a combination of shoving forward and shouldering aside previously deposited debris and through progressive vertical accretion. Progressive accretion by the experimental flows is contrary to commonly assumed en masse sedimentation by debris flows. Despite progressive sediment emplacement, deposits were composed of unstratified accumulations of generally unsorted debris; hence massively textured, poorly sorted debris-flow deposits are not emplaced uniquely en masse. The depositional process was recorded mainly by deposit morphology and surface texture and was not faithfully registered by interior sedimentary texture; homogeneous internal textures could be misinterpreted as the result of en masse emplacement by a single surge. Deposition of sediment by similar, yet separate, debris flows produced a homogenous, massively textured composite deposit having little stratigraphic distinction. Similar deposit characteristics and textures are observed in natural debris-flow deposits. Experimental production of massively textured deposits by progressive sediment accretion limits interpretations that can be drawn from deposit characteristics and casts doubt on methods of estimating flow properties from deposit thickness or from relations between particle size and bed thickness.

  9. 4 CFR 22.11 - Depositions [Rule 11].

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 4 Accounts 1 2011-01-01 2011-01-01 false Depositions [Rule 11]. 22.11 Section 22.11 Accounts... OFFICE CONTRACT APPEALS BOARD § 22.11 Depositions [Rule 11]. (a) When depositions may be taken. After an... of any person by deposition upon oral examination or written questions, for the purpose of discovery...

  10. 4 CFR 22.11 - Depositions [Rule 11].

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 4 Accounts 1 2010-01-01 2010-01-01 false Depositions [Rule 11]. 22.11 Section 22.11 Accounts... OFFICE CONTRACT APPEALS BOARD § 22.11 Depositions [Rule 11]. (a) When depositions may be taken. After an... of any person by deposition upon oral examination or written questions, for the purpose of discovery...

  11. Magma ascent, fragmentation and depositional characteristics of "dry" maar volcanoes: Similarities with vent-facies kimberlite deposits

    NASA Astrophysics Data System (ADS)

    Berghuijs, Jaap F.; Mattsson, Hannes B.

    2013-02-01

    Several maar craters within the Lake Natron-Engaruka monogenetic volcanic field (LNE-MVF) of northern Tanzania show compelling evidence for magmatic fragmentation and dry deposition. This is in contradiction of the common belief that most maars are formed through the explosive interaction between ascending magma and ground- or surface water. We here present a detailed study on the eruptive and depositional characteristics of the Loolmurwak and Eledoi maar volcanoes, two of the largest craters in the LNE-MVF, focusing on high-resolution stratigraphy, sedimentology, grain size distribution, pyroclast textures and morphologies, bulk geochemistry and mineral chemistry. At both maars, ejected material has been emplaced by a combination of pyroclastic surges and fallout. Indicators of phreatomagmatic fragmentation and wet deposition, such as impact sags, accretionary lapilli, vesiculated tuffs and plastering against obstacles, are absent in the deposits. Juvenile material predominantly occurs as fluidal-shaped vesicular melt droplets and contains no glass shards produced by the breakage of bubble walls. The Eledoi deposits comprise a large amount of inversely graded beds and lenses, which result from grain flow in a dry depositional environment. Preferential deposition of fine material toward the northern side of its crater can be related to effective wind winnowing in a dry eruption plume. This large variety of observations testifies to the dominance of magmatic fragmentation as well as dry deposition at the Loolmurwak and Eledoi maars, which is in line with what has been found for other structures in the LNE-MVF but contrasts with current ideas on maar formation. We infer that a volatile-rich, olivine melilitic magma was formed by small amounts of partial melting at upper mantle depths. With minimum average ascent rates of 5.3 m s- 1 for Loolmurwak and 26.2 m s- 1 for Eledoi, this magma rapidly moved toward the surface and exsolved a substantial amount of volatiles

  12. Climax-Type Porphyry Molybdenum Deposits

    USGS Publications Warehouse

    Ludington, Steve; Plumlee, Geoffrey S.

    2009-01-01

    Climax-type porphyry molybdenum deposits, as defined here, are extremely rare; thirteen deposits are known, all in western North America and ranging in age from Late Cretaceous to mainly Tertiary. They are consistently found in a postsubduction, extensional tectonic setting and are invariably associated with A-type granites that formed after peak activity of a magmatic cycle. The deposits consist of ore shells of quartz-molybdenite stockwork veins that lie above and surrounding the apices of cupola-like, highly evolved, calc-alkaline granite and subvolcanic rhyolite-porphyry bodies. These plutons are invariably enriched in fluorine (commonly >1 percent), rubidium (commonly >500 parts per million), and niobium-tantalum (Nb commonly >50 parts per million). The deposits are relatively high grade (typically 0.1-0.3 percent Mo) and may be very large (typically 100-1,000 million tons). Molybdenum, as MoS2, is the primary commodity in all known deposits. The effect on surface-water quality owing to natural influx of water or sediment from a Climax-type mineralized area can extend many kilometers downstream from the mineralized area. Waste piles composed of quartz-silica-pyrite altered rocks will likely produce acidic drainage waters. The potential exists for concentrations of fluorine or rare metals in surface water and groundwater to exceed recommended limits for human consumption near both mined and unmined Climax-type deposits.

  13. Rare earth element deposits in China

    USGS Publications Warehouse

    Xie, Yu-Ling; Hou, Zeng-qian; Goldfarb, Richard J.; Guo, Xiang; Wang, Lei

    2016-01-01

    China is the world’s leading rare earth element (REE) producer and hosts a variety of deposit types. Carbonatite- related REE deposits, the most significant deposit type, include two giant deposits presently being mined in China, Bayan Obo and Maoniuping, the first and third largest deposits of this type in the world, respectively. The carbonatite-related deposits host the majority of China’s REE resource and are the primary supplier of the world’s light REE. The REE-bearing clay deposits, or ion adsorption-type deposits, are second in importance and are the main source in China for heavy REE resources. Other REE resources include those within monazite or xenotime placers, beach placers, alkaline granites, pegmatites, and hydrothermal veins, as well as some additional deposit types in which REE are recovered as by-products. Carbonatite-related REE deposits in China occur along craton margins, both in rifts (e.g., Bayan Obo) and in reactivated transpressional margins (e.g., Maoniuping). They comprise those along the northern, eastern, and southern margins of the North China block, and along the western margin of the Yangtze block. Major structural features along the craton margins provide first-order controls for REE-related Proterozoic to Cenozoic carbonatite alkaline complexes; these are emplaced in continental margin rifts or strike-slip faults. The ion adsorption-type REE deposits, mainly situated in the South China block, are genetically linked to the weathering of granite and, less commonly, volcanic rocks and lamprophyres. Indosinian (early Mesozoic) and Yanshanian (late Mesozoic) granites are the most important parent rocks for these REE deposits, although Caledonian (early Paleozoic) granites are also of local importance. The primary REE enrichment is hosted in various mineral phases in the igneous rocks and, during the weathering process, the REE are released and adsorbed by clay minerals in the weathering profile. Currently, these REE-rich clays are

  14. 12 CFR 263.53 - Discovery depositions.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 4 2014-01-01 2014-01-01 false Discovery depositions. 263.53 Section 263.53... Discovery depositions. (a) In general. In addition to the discovery permitted in subpart A of this part, limited discovery by means of depositions shall be allowed for individuals with knowledge of facts...

  15. 12 CFR 263.53 - Discovery depositions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 4 2012-01-01 2012-01-01 false Discovery depositions. 263.53 Section 263.53... Discovery depositions. (a) In general. In addition to the discovery permitted in subpart A of this part, limited discovery by means of depositions shall be allowed for individuals with knowledge of facts...

  16. Focused helium-ion-beam-induced deposition

    NASA Astrophysics Data System (ADS)

    Alkemade, P. F. A.; Miro, H.

    2014-12-01

    The recent introduction of the helium ion microscope (HIM) offers new possibilities for materials modification and fabrication with spatial resolution below 10 nm. In particular, the specific interaction of He+ ions in the tens of keV energy range with materials—i.e., minimal deflection and mainly energy loss via electronic excitations—renders the HIM a special tool for ion-beam-induced deposition. In this work, an overview is given of all studies of helium-ion-beam-induced deposition (He-IBID) that appeared in the literature before summer 2014. Continuum models that describe the deposition processes are presented in detail, with emphasis on precursor depletion and replenishment. In addition, a Monte Carlo model is discussed. Basic experimental He-IBID studies are critically examined. They show deposition rates of up to 0.1 nm3/ion. Analysis by means of a continuum model yields the precursor diffusion constant and the cross sections for beam-induced precursor decomposition and beam-induced desorption. Moreover, it is shown that deposition takes place only in a small zone around the beam impact point. Furthermore, the characterization of deposited materials is discussed in terms of microstructure and resistivity. It is shown that He-IBID material resembles more electron-beam-induced-deposition (EBID) material than Ga-ion-beam-induced-deposition (Ga-IBID) material. Nevertheless, the spatial resolution for He-IBID is in general better than for EBID and Ga-IBID; in particular, proximity effects are minimal.

  17. Axial distribution of plasma fluctuations, plasma parameters, deposition rate and grain size during copper deposition

    NASA Astrophysics Data System (ADS)

    Gopikishan, S.; Banerjee, I.; Pathak, Anand; Mahapatra, S. K.

    2017-08-01

    Floating potential fluctuations, plasma parameters and deposition rate have been investigated as a function of axial distance during deposition of copper in direct current (DC) magnetron sputtering system. Fluctuations were analyzed using phase space, power spectra and amplitude bifurcation plots. It has been observed that the fluctuations are modified from chaotic to ordered state with increase in the axial distance from cathode. Plasma parameters such as electron density (ne), electron temperature (Te) and deposition rate (Dr) were measured and correlated with plasma fluctuations. It was found that more the deposition rate, greater the grain size, higher the electron density, higher the electron temperature and more chaotic the oscillations near the cathode. This observation could be helpful to the thin film technology industry to optimize the required film.

  18. 22 CFR 92.62 - Captioning and certifying depositions.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 22 Foreign Relations 1 2011-04-01 2011-04-01 false Captioning and certifying depositions. 92.62... SERVICES Depositions and Letters Rogatory § 92.62 Captioning and certifying depositions. The notarizing officer should prepare a caption for every deposition; should certify on the deposition that the witness...

  19. 22 CFR 92.62 - Captioning and certifying depositions.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 22 Foreign Relations 1 2010-04-01 2010-04-01 false Captioning and certifying depositions. 92.62... SERVICES Depositions and Letters Rogatory § 92.62 Captioning and certifying depositions. The notarizing officer should prepare a caption for every deposition; should certify on the deposition that the witness...

  20. 12 CFR 217.101 - Premiums on deposits.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... AGAINST THE PAYMENT OF INTEREST ON DEMAND DEPOSITS (REGULATION Q) Interpretations § 217.101 Premiums on... from paying interest on a demand deposit. Premiums, whether in the form of merchandise, credit, or cash... exceed $10 for deposits of less than $5,000 or $20 for deposits of $5,000 or more. The costs of premiums...

  1. Laser assisted deposition

    NASA Technical Reports Server (NTRS)

    Dutta, S.

    1983-01-01

    Applications of laser-based processing techniques to solar cell metallization are discussed. Laser-assisted thermal or photolytic maskless deposition from organometallic vapors or solutions may provide a viable alternative to photovoltaic metallization systems currently in use. High power, defocused excimer lasers may be used in conjunction with masks as an alternative to direct laser writing to provide higher throughput. Repeated pulsing with excimer lasers may eliminate the need for secondary plating techniques for metal film buildup. A comparison between the thermal and photochemical deposition processes is made.

  2. Sinks for Inorganic Nitrogen Deposition in Forest Ecosystems with Low and High Nitrogen Deposition in China

    PubMed Central

    Sheng, Wenping; Yu, Guirui; Fang, Huajun; Jiang, Chunming; Yan, Junhua; Zhou, Mei

    2014-01-01

    We added the stable isotope 15N in the form of (15NH4)2SO4 and K15NO3 to forest ecosystems in eastern China under two different N deposition levels to study the fate of the different forms of deposited N. Prior to the addition of the 15N tracers, the natural 15N abundance ranging from −3.4‰ to +10.9‰ in the forest under heavy N deposition at Dinghushan (DHS), and from −3.92‰ to +7.25‰ in the forest under light N deposition at Daxinganling (DXAL). Four months after the tracer application, the total 15N recovery from the major ecosystem compartments ranged from 55.3% to 90.5%. The total 15N recoveries were similar under the (15NH4)2SO4 tracer treatment in both two forest ecosystems, whereas the total 15N recovery was significantly lower in the subtropical forest ecosystem at DHS than in the boreal forest ecosystem at DXAL under the K15NO3 tracer treatment. The 15N assimilated into the tree biomass represented only 8.8% to 33.7% of the 15N added to the forest ecosystems. In both of the tracer application treatments, more 15N was recovered from the tree biomass in the subtropical forest ecosystem at DHS than the boreal forest ecosystem at DXAL. The amount of 15N assimilated into tree biomass was greater under the K15NO3 tracer treatment than that of the (15NH4)2SO4 treatment in both forest ecosystems. This study suggests that, although less N was immobilized in the forest ecosystems under more intensive N deposition conditions, forest ecosystems in China strongly retain N deposition, even in areas under heavy N deposition intensity or in ecosystems undergoing spring freezing and thawing melts. Compared to ammonium deposition, deposited nitrate is released from the forest ecosystem more easily. However, nitrate deposition could be retained mostly in the plant N pool, which might lead to more C sequestration in these ecosystems. PMID:24586688

  3. 12 CFR 263.53 - Discovery depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 12 Banks and Banking 3 2011-01-01 2011-01-01 false Discovery depositions. 263.53 Section 263.53... depositions. (a) In general. In addition to the discovery permitted in subpart A of this part, limited discovery by means of depositions shall be allowed for individuals with knowledge of facts material to the...

  4. 12 CFR 263.53 - Discovery depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 3 2010-01-01 2010-01-01 false Discovery depositions. 263.53 Section 263.53... depositions. (a) In general. In addition to the discovery permitted in subpart A of this part, limited discovery by means of depositions shall be allowed for individuals with knowledge of facts material to the...

  5. 49 CFR 510.6 - Administrative depositions.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    .... (4) Objections to the qualifications of the officer taking the deposition, or to the manner of taking... the objections. Errors and irregularities occurring at a deposition in the manner of the taking of the... reasonable objection is made thereto at the taking of the deposition. (5) If the witness refuses to answer...

  6. 24 CFR 891.435 - Security deposits.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 24 Housing and Urban Development 4 2013-04-01 2013-04-01 false Security deposits. 891.435 Section... Security deposits. This section shall apply to capital advances under the Section 202 Program and the... subpart E of this part, the requirements in § 891.635 also apply. (a) Collection of security deposits. At...

  7. 26 CFR 2.1-11 - Time deposits.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 26 Internal Revenue 14 2012-04-01 2012-04-01 false Time deposits. 2.1-11 Section 2.1-11 Internal... CONSTRUCTION RESERVE FUND § 2.1-11 Time deposits. Deposits in the construction reserve fund not invested in securities may be placed in time deposits when, in the judgment of the taxpayer, it is desirable and feasible...

  8. 26 CFR 2.1-11 - Time deposits.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 26 Internal Revenue 14 2014-04-01 2013-04-01 true Time deposits. 2.1-11 Section 2.1-11 Internal... CONSTRUCTION RESERVE FUND § 2.1-11 Time deposits. Deposits in the construction reserve fund not invested in securities may be placed in time deposits when, in the judgment of the taxpayer, it is desirable and feasible...

  9. 26 CFR 2.1-11 - Time deposits.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 26 Internal Revenue 14 2013-04-01 2013-04-01 false Time deposits. 2.1-11 Section 2.1-11 Internal... CONSTRUCTION RESERVE FUND § 2.1-11 Time deposits. Deposits in the construction reserve fund not invested in securities may be placed in time deposits when, in the judgment of the taxpayer, it is desirable and feasible...

  10. Deposition of intranasal glucocorticoids--preliminary study.

    PubMed

    Rapiejko, Piotr; Sosnowski, Tomasz R; Sova, Jarosław; Jurkiewicz, Dariusz

    2015-01-01

    Intranasal glucocorticoids are the treatment of choice in the therapy of rhinitis. The differences in efficiency of particular medications proven by therapeutic index may result from differences in composition of particular formulations as well as from diverse deposition in nasal cavities. Intranasal formulations of glucocorticoids differ in volume of a single dose in addition to variety in density, viscosity and dispenser nozzle structure. The aim of this report was to analyze the deposition of most often used intranasal glucocorticoids in the nasal cavity and assessment of the usefulness of a nose model from a 3D printer reflecting anatomical features of a concrete patient. Three newest and most often used in Poland intranasal glucocorticoids were chosen to analysis; mometasone furoate (MF), fluticasone propionate (FP) and fluticasone furoate (FF). Droplet size distribution obtained from the tested formulations was determined by use of a laser aerosol spectrometer Spraytec (Malvern Instruments, UK). The model of the nasal cavity was obtained using a 3D printer. The printout was based upon a tridimensional reconstruction of nasal cavity created on the basis of digital processing of computed tomography of paranasal sinuses. The deposition of examined medications was established by a method of visualization combined with image analysis using commercial substance which colored itself intensively under the influence of water being the dominant ingredient of all tested preparations. On the basis of obtained results regions of dominating deposition of droplets of intranasal medication on the wall and septum of the nasal cavity were compared. Droplet size of aerosol of tested intranasal medications typically lies within the range of 25-150 µm. All tested medications deposited mainly on the anterior part of inferior turbinate. FP preparation deposited also on the anterior part of the middle nasal turbinate, marginally embracing a fragment of the central part of this

  11. Ultraviolet optical properties of aluminum fluoride thin films deposited by atomic layer deposition

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

    Hennessy, John, E-mail: john.j.hennessy@jpl.nasa.gov; Jewell, April D.; Balasubramanian, Kunjithapatham

    2016-01-15

    Aluminum fluoride (AlF{sub 3}) is a low refractive index material with promising optical applications for ultraviolet (UV) wavelengths. An atomic layer deposition process using trimethylaluminum and anhydrous hydrogen fluoride has been developed for the deposition of AlF{sub 3} at substrate temperatures between 100 and 200 °C. This low temperature process has resulted in thin films with UV-optical properties that have been characterized by ellipsometric and reflection/transmission measurements at wavelengths down to 200 nm. The optical loss for 93 nm thick films deposited at 100 °C was measured to be less than 0.2% from visible wavelengths down to 200 nm, and additional microstructural characterization demonstrates thatmore » the films are amorphous with moderate tensile stress of 42–105 MPa as deposited on silicon substrates. X-ray photoelectron spectroscopy analysis shows no signature of residual aluminum oxide components making these films good candidates for a variety of applications at even shorter UV wavelengths.« less

  12. Gold in placer deposits

    USGS Publications Warehouse

    Yeend, Warren; Shawe, Daniel R.; Wier, Kenneth L.

    1989-01-01

    Man most likely first obtained gold from placer deposits, more than 6,000 years ago. Placers account for more than two-thirds of the total world gold supply, and roughly half of that mined in the States of California, Alaska, Montana, and Idaho.Placer deposits result from weathering and release of gold from lode deposits, transportation of the gold, and concentration of the gold dominantly in stream gravels. Unless preserved by burial, a placer subsequently may be eroded, and either dispersed or reconcentrated.California has produced more than 40 million troy ounces of gold from placers, both modern and fossil (Tertiary). The source of the great bulk of the gold is numerous quartz veins and mineralized zones of the Mother Lode and related systems in the western Sierra Nevada region. The gold-bearing lodes were emplaced in Carboniferous and Jurassic metamorphic rocks intruded by small bodies of Jurassic and Cretaceous igneous rocks. Mineralization occurred probably in Late Cretaceous time. Significant amounts of placer gold also were mined along the Salmon and Trinity Rivers in northern California. Source of the gold is lode deposits in Paleozoic and Mesozoic metamorphic rocks that were intruded by Mesozoic igneous rocks.Alaska has produced roughly 21 million ounces of gold from placer deposits. Most (about 13 million ounces) has come from the interior region, including 7,600,000 ounces from the Fairbanks district and 1,300,000 ounces from the Iditarod district. Lode sources are believed to be mostly quartz veins in Precambrian or Paleozoic metamorphic rocks intruded by small igneous bodies near Fairbanks, and shear zones in Tertiary(?) quartz monzonite stocks at Iditarod. The Seward Peninsula has produced more than 6 million ounces of placer gold, including about 4,000,000 ounces from the Nome district. Most of the gold was derived from raised beach deposits. Source of the gold probably is Tertiary-mineralized faults and joints in metamorphic rocks of late

  13. Study on electrochemically deposited Mg metal

    NASA Astrophysics Data System (ADS)

    Matsui, Masaki

    An electrodeposition process of magnesium metal from Grignard reagent based electrolyte was studied by comparing with lithium. The electrodeposition of magnesium was performed at various current densities. The obtained magnesium deposits did not show dendritic morphologies while all the lithium deposits showed dendritic products. Two different crystal growth modes in the electrodeposition process of magnesium metal were confirmed by an observation using scanning electron micro scope (SEM) and a crystallographic analysis using X-ray diffraction (XRD). An electrochemical study of the deposition/dissolution process of the magnesium showed a remarkable dependency of the overpotential of magnesium deposition on the electrolyte concentration compared with lithium. This result suggests that the dependency of the overpotential on the electrolyte concentration prevent the locally concentrated current resulting to form very uniform deposits.

  14. 29 CFR 102.30 - Examination of witnesses; deposition.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 2 2010-07-01 2010-07-01 false Examination of witnesses; deposition. 102.30 Section 102.30..., Depositions, and Subpoenas § 102.30 Examination of witnesses; deposition. Witnesses shall be examined orally... by deposition. (a) Applications to take depositions shall be in writing setting forth the reasons why...

  15. 29 CFR 102.30 - Examination of witnesses; deposition.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 2 2011-07-01 2011-07-01 false Examination of witnesses; deposition. 102.30 Section 102.30..., Depositions, and Subpoenas § 102.30 Examination of witnesses; deposition. Witnesses shall be examined orally... by deposition. (a) Applications to take depositions shall be in writing setting forth the reasons why...

  16. Ambient Ammonium Contribution to total Nitrogen Deposition ...

    EPA Pesticide Factsheets

    There has been a wealth of evidence over the last decade illustrating the rising importance of reduced inorganic nitrogen (NHx = ammonia gas, NH3, plus particulate ammonium, p-NH4) in the overall atmospheric mass balance and deposition of nitrogen as emissions of oxidized nitrogen have decreased throughout a period of stable or increasing NH3 emissions. In addition, the fraction of ambient ammonia relative to p-NH4 generally has risen as a result of decreases in both oxides of nitrogen and sulfur emissions. EPA plans to consider ecological effects related to deposition of nitrogen, of which NHx is a contributing component, in the review of secondary National Ambient Air Quality Standards (NAAQS) for oxides of nitrogen and sulfur (NOx/SOx standard). Although these ecological effects are associated with total nitrogen deposition, it will be important to understand the emissions sources contributing to the total nitrogen deposition and to understand how much of the total nitrogen deposition is from deposition of NHx versus other nitrogen species. Because p-NH4 contributes to nitrogen deposition and can also be a significant component of particulate matter, there is a potential overlap in addressing nitrogen based deposition effects in the secondary PM and NOx/SOx NAAQS. Consequently, there is a policy interest in quantifying the contribution of p-NH4 to total nitrogen deposition. While dry deposition of p-NH4 is calculated through a variety of modeling app

  17. Improved mapping of National Atmospheric Deposition Program wet-deposition in complex terrain using PRISM-gridded data sets

    USGS Publications Warehouse

    Latysh, Natalie E.; Wetherbee, Gregory Alan

    2012-01-01

    High-elevation regions in the United States lack detailed atmospheric wet-deposition data. The National Atmospheric Deposition Program/National Trends Network (NADP/NTN) measures and reports precipitation amounts and chemical constituent concentration and deposition data for the United States on annual isopleth maps using inverse distance weighted (IDW) interpolation methods. This interpolation for unsampled areas does not account for topographic influences. Therefore, NADP/NTN isopleth maps lack detail and potentially underestimate wet deposition in high-elevation regions. The NADP/NTN wet-deposition maps may be improved using precipitation grids generated by other networks. The Parameter-elevation Regressions on Independent Slopes Model (PRISM) produces digital grids of precipitation estimates from many precipitation-monitoring networks and incorporates influences of topographical and geographical features. Because NADP/NTN ion concentrations do not vary with elevation as much as precipitation depths, PRISM is used with unadjusted NADP/NTN data in this paper to calculate ion wet deposition in complex terrain to yield more accurate and detailed isopleth deposition maps in complex terrain. PRISM precipitation estimates generally exceed NADP/NTN precipitation estimates for coastal and mountainous regions in the western United States. NADP/NTN precipitation estimates generally exceed PRISM precipitation estimates for leeward mountainous regions in Washington, Oregon, and Nevada, where abrupt changes in precipitation depths induced by topography are not depicted by IDW interpolation. PRISM-based deposition estimates for nitrate can exceed NADP/NTN estimates by more than 100% for mountainous regions in the western United States.

  18. Improved mapping of National Atmospheric Deposition Program wet-deposition in complex terrain using PRISM-gridded data sets.

    PubMed

    Latysh, Natalie E; Wetherbee, Gregory Alan

    2012-01-01

    High-elevation regions in the United States lack detailed atmospheric wet-deposition data. The National Atmospheric Deposition Program/National Trends Network (NADP/NTN) measures and reports precipitation amounts and chemical constituent concentration and deposition data for the United States on annual isopleth maps using inverse distance weighted (IDW) interpolation methods. This interpolation for unsampled areas does not account for topographic influences. Therefore, NADP/NTN isopleth maps lack detail and potentially underestimate wet deposition in high-elevation regions. The NADP/NTN wet-deposition maps may be improved using precipitation grids generated by other networks. The Parameter-elevation Regressions on Independent Slopes Model (PRISM) produces digital grids of precipitation estimates from many precipitation-monitoring networks and incorporates influences of topographical and geographical features. Because NADP/NTN ion concentrations do not vary with elevation as much as precipitation depths, PRISM is used with unadjusted NADP/NTN data in this paper to calculate ion wet deposition in complex terrain to yield more accurate and detailed isopleth deposition maps in complex terrain. PRISM precipitation estimates generally exceed NADP/NTN precipitation estimates for coastal and mountainous regions in the western United States. NADP/NTN precipitation estimates generally exceed PRISM precipitation estimates for leeward mountainous regions in Washington, Oregon, and Nevada, where abrupt changes in precipitation depths induced by topography are not depicted by IDW interpolation. PRISM-based deposition estimates for nitrate can exceed NADP/NTN estimates by more than 100% for mountainous regions in the western United States.

  19. 76 FR 7740 - Amendments to Deposit Insurance Regulations: Deposit Insurance Coverage Training; SMDIA Notification

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-11

    ... accounts and/ or respond to customer questions about FDIC insurance coverage (hereafter ``employees... new deposit account, inquire whether the customer has an ownership interest in any other account at the IDI and, if so, whether the customer's aggregate ownership interest in deposit accounts, including...

  20. Simulating ozone dry deposition at a boreal forest with a multi-layer canopy deposition model

    NASA Astrophysics Data System (ADS)

    Zhou, Putian; Ganzeveld, Laurens; Rannik, Üllar; Zhou, Luxi; Gierens, Rosa; Taipale, Ditte; Mammarella, Ivan; Boy, Michael

    2017-01-01

    A multi-layer ozone (O3) dry deposition model has been implemented into SOSAA (a model to Simulate the concentrations of Organic vapours, Sulphuric Acid and Aerosols) to improve the representation of O3 concentration and flux within and above the forest canopy in the planetary boundary layer. We aim to predict the O3 uptake by a boreal forest canopy under varying environmental conditions and analyse the influence of different factors on total O3 uptake by the canopy as well as the vertical distribution of deposition sinks inside the canopy. The newly implemented dry deposition model was validated by an extensive comparison of simulated and observed O3 turbulent fluxes and concentration profiles within and above the boreal forest canopy at SMEAR II (Station to Measure Ecosystem-Atmosphere Relations II) in Hyytiälä, Finland, in August 2010. In this model, the fraction of wet surface on vegetation leaves was parametrised according to the ambient relative humidity (RH). Model results showed that when RH was larger than 70 % the O3 uptake onto wet skin contributed ˜ 51 % to the total deposition during nighttime and ˜ 19 % during daytime. The overall contribution of soil uptake was estimated about 36 %. The contribution of sub-canopy deposition below 4.2 m was modelled to be ˜ 38 % of the total O3 deposition during daytime, which was similar to the contribution reported in previous studies. The chemical contribution to O3 removal was evaluated directly in the model simulations. According to the simulated averaged diurnal cycle the net chemical production of O3 compensated up to ˜ 4 % of dry deposition loss from about 06:00 to 15:00 LT. During nighttime, the net chemical loss of O3 further enhanced removal by dry deposition by a maximum ˜ 9 %. Thus the results indicated an overall relatively small contribution of airborne chemical processes to O3 removal at this site.

  1. Friction and Wear of Ion-Beam-Deposited Diamondlike Carbon on Chemical-Vapor-Deposited, Fine-Grain Diamond

    NASA Technical Reports Server (NTRS)

    Miyoshi, Kazuhisa; Wu, Richard L. C.; Lanter, William C.

    1996-01-01

    Friction and wear behavior of ion-beam-deposited diamondlike carbon (DLC) films coated on chemical-vapor-deposited (CVD), fine-grain diamond coatings were examined in ultrahigh vacuum, dry nitrogen, and humid air environments. The DLC films were produced by the direct impact of an ion beam (composed of a 3:17 mixture of Ar and CH4) at ion energies of 1500 and 700 eV and an RF power of 99 W. Sliding friction experiments were conducted with hemispherical CVD diamond pins sliding on four different carbon-base coating systems: DLC films on CVD diamond; DLC films on silicon; as-deposited, fine-grain CVD diamond; and carbon-ion-implanted, fine-grain CVD diamond on silicon. Results indicate that in ultrahigh vacuum the ion-beam-deposited DLC films on fine-grain CVD diamond (similar to the ion-implanted CVD diamond) greatly decrease both the friction and wear of fine-grain CVD diamond films and provide solid lubrication. In dry nitrogen and in humid air, ion-beam-deposited DLC films on fine-grain CVD diamond films also had a low steady-state coefficient of friction and a low wear rate. These tribological performance benefits, coupled with a wider range of coating thicknesses, led to longer endurance life and improved wear resistance for the DLC deposited on fine-grain CVD diamond in comparison to the ion-implanted diamond films. Thus, DLC deposited on fine-grain CVD diamond films can be an effective wear-resistant, lubricating coating regardless of environment.

  2. Automatic chemical vapor deposition

    NASA Technical Reports Server (NTRS)

    Kennedy, B. W.

    1981-01-01

    Report reviews chemical vapor deposition (CVD) for processing integrated circuits and describes fully automatic machine for CVD. CVD proceeds at relatively low temperature, allows wide choice of film compositions (including graded or abruptly changing compositions), and deposits uniform films of controllable thickness at fairly high growth rate. Report gives overview of hardware, reactants, and temperature ranges used with CVD machine.

  3. Deposit formation in hydrocarbon rocket fuels

    NASA Technical Reports Server (NTRS)

    Roback, R.; Szetela, E. J.; Spadaccini, L. J.

    1981-01-01

    An experimental program was conducted to study deposit formation in hydrocarbon fuels under flow conditions that exist in high-pressure, rocket engine cooling systems. A high pressure fuel coking test apparatus was designed and developed and was used to evaluate thermal decomposition (coking) limits and carbon deposition rates in heated copper tubes for two hydrocarbon rocket fuels, RP-1 and commercial-grade propane. Tests were also conducted using JP-7 and chemically-pure propane as being representative of more refined cuts of the baseline fuels. A parametric evaluation of fuel thermal stability was performed at pressures of 136 atm to 340 atm, bulk fuel velocities in the range 6 to 30 m/sec, and tube wall temperatures in the range 422 to 811 K. Results indicated that substantial deposit formation occurs with RP-1 fuel at wall temperatures between 600 and 800 K, with peak deposit formation occurring near 700 K. No improvements were obtained when deoxygenated JP-7 fuel was substituted for RP-1. The carbon deposition rates for the propane fuels were generally higher than those obtained for either of the kerosene fuels at any given wall temperature. There appeared to be little difference between commercial-grade and chemically-pure propane with regard to type and quantity of deposit. Results of tests conducted with RP-1 indicated that the rate of deposit formation increased slightly with pressure over the range 136 atm to 340 atm. Finally, lating the inside wall of the tubes with nickel was found to significantly reduce carbon deposition rates for RP-1 fuel.

  4. Glacial-eustatic/climatic model for Upper Pennsylvanian marine and nonmarine cyclothems in the Appalachian basin

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

    Heckel, P.H.

    1992-01-01

    Only glacial-eustatic sea-level fluctuations can account for all the characteristics of Upper Pennsylvanian marine cyclothems in the Midcontinent. Because this control is global, it must have affected deposition during this time everywhere. In the Appalachian basin widespread well developed paleosols represent long-term sea-level lowstand. During Conemaugh marine incursions, rising sea level ponded fresh-water influx to form peat swamps that migrated landward ahead of transgression and produced early transgressive coals. Marine highstand deposits commonly are conodont-rich limestones, typically skeletal packstone with glaucony and phosphorite. Regression resulted in progradation of detrital shorelines with local delta cycles, followed eventually by more paleosol formationmore » and local erosional incision that removed older sediments including the marine units in places. Fluvial sands filled many of these channels. During Monongahela deposition when marine incursions no longer entered the Appalachian basin, the climatic fluctuations recognized by Cecil can reasonably be related to sea-level fluctuations nearby, but with shifts in climatic significance of gross lithotopes. Coal swamps would more likely have formed at maximum marine highstand when the nearby sea would have provided both high base level and an abundant source of rainfall. Nonmarine limestones would more likely have formed at maximum lowstand when the sea was most distant and the climate driest. The intervening detrital deposits between the coals and limestones formed under intermediate seasonal rainfall regimes during both marine transgression and regression farther west in the Midcontinent. Conemaugh and Allegheny coals without overlying marine units probably also represent mainly marine highstand elsewhere, and nonmarine limestones of these ages typically are associated with lowstand paleosols.« less

  5. Structural characterization of MAPLE deposited lipase biofilm

    NASA Astrophysics Data System (ADS)

    Aronne, Antonio; Ausanio, Giovanni; Bloisi, Francesco; Calabria, Raffaela; Califano, Valeria; Fanelli, Esther; Massoli, Patrizio; Vicari, Luciano R. M.

    2014-11-01

    Lipases (triacylglycerol ester hydrolases) are enzymes used in several industrial applications. Enzymes immobilization can be used to address key issues limiting widespread application at industrial level. Immobilization efficiency is related to the ability to preserve the native conformation of the enzyme. MAPLE (Matrix Assisted Pulsed Laser Evaporation) technique, a laser deposition procedure for treating organic/polymeric/biomaterials, was applied for the deposition of lipase enzyme in an ice matrix, using near infrared laser radiation. Microscopy analysis showed that the deposition occurred in micrometric and submicrometric clusters with a wide size distribution. AFM imaging showed that inter-cluster regions are uniformly covered with smaller aggregates of nanometric size. Fourier transform infrared spectroscopy was used for both recognizing the deposited material and analyzing its secondary structure. Results showed that the protein underwent reversible self-association during the deposition process. Actually, preliminary tests of MAPLE deposited lipase used for soybean oil transesterification with isopropyl alcohol followed by gas chromatography-mass spectrometry gave results consistent with undamaged deposition of lipase.

  6. Vapor-deposited porous films for energy conversion

    DOEpatents

    Jankowski, Alan F.; Hayes, Jeffrey P.; Morse, Jeffrey D.

    2005-07-05

    Metallic films are grown with a "spongelike" morphology in the as-deposited condition using planar magnetron sputtering. The morphology of the deposit is characterized by metallic continuity in three dimensions with continuous and open porosity on the submicron scale. The stabilization of the spongelike morphology is found over a limited range of the sputter deposition parameters, that is, of working gas pressure and substrate temperature. This spongelike morphology is an extension of the features as generally represented in the classic zone models of growth for physical vapor deposits. Nickel coatings were deposited with working gas pressures up 4 Pa and for substrate temperatures up to 1000 K. The morphology of the deposits is examined in plan and in cross section views with scanning electron microscopy (SEM). The parametric range of gas pressure and substrate temperature (relative to absolute melt point) under which the spongelike metal deposits are produced appear universal for other metals including gold, silver, and aluminum.

  7. Texture and depositional history of near-surface alluvial deposits in the central part of the western San Joaquin Valley, California

    USGS Publications Warehouse

    Laudon, Julie; Belitz, Kenneth

    1989-01-01

    Saline conditions and associated high levels of selenium and other soluble trace elements in soil, shallow ground water, and agricultural drain water of the western San Joaquin Valley, California, have prompted a study of the texture of near-surface alluvial deposits in the central part of the western valley. Texture is characterized by the percentage of coarse-grained sediment present within a specified subsurface depth interval and is used as a basis for mapping the upper 50 feet of deposits. Resulting quantitative descriptions of the deposits are used to interpret the late Quaternary history of the area. Three hydrogeologic units--Coast Range alluvium, flood-basin deposits, and Sierran sand--can be recognized in the upper 50 feet of deposits in the central part of the western San Joaquin Valley. The upper 30 feet of Coast Range alluvium and the adjacent 5 to 35 feet of flood-basin deposits are predominantly fine grained. These fine-grained Coast Range deposits are underlain by coarse-grained channel deposits. The fine-grained flood basin deposits are underlain by coarse-grained Sierran sand. The extent and orientation of channel deposits below 20 feet in the Coast Range alluvium indicate that streams draining the Coast Range may have been tributary to the axial stream that deposited the Sierran sand and that streamflow may have been to the southeast. The fining-upward stratigraphic sequence in the upper 50 feet of deposits and the headward retreat of tributary stream channels from the valley trough with time support a recent hypothesis of climatic control of alluviation in the western San Joaquin Valley.

  8. Origin of bonebeds in Quaternary tank deposits

    NASA Astrophysics Data System (ADS)

    Araújo-Júnior, Hermínio Ismael de; Porpino, Kleberson de Oliveira; Bergqvist, Lílian Paglarelli

    2017-07-01

    Tank deposits are an exceptional type of fossiliferous deposit and bear a remarkably fossil record of the Pleistocene megafauna of South America, particularly of Brazil. The taphonomy of vertebrate remains preserved in this type of environmental context was clearly driven by climate, similarly to most of the Quaternary continental fossil record. The formation of the vertebrates fossil record in tank deposits was influenced by the climate seasonality typical of arid climate. The taphonomic history of most tank deposits is a consequence of this seasonality and, as a result, the paleoecological data preserved in their fossil assemblages is reliable with respect to paleobiological and paleoenvironmental settings of the Quaternary ecosystems of the Brazilian Intertropical Region (BIR). Other tank deposits experienced an unusual taphonomic history that, besides climate, was affected by recurrent events of reworking produced by the depositional agents dominant in the surrounding alluvial plains. The conclusions obtained here concerning the main taphonomic settings and formative processes that characterize fossil vertebrate assemblages of tank deposits will help further studies aimed to recover information on the paleoecology of Quaternary fauna collected in such deposits by allowing a better understanding of their time and spatial resolutions and other potential biases.

  9. Gigantic landslides versus glacial deposits: on origin of large hummock deposits in Alai Valley, Northern Pamir

    NASA Astrophysics Data System (ADS)

    Reznichenko, Natalya

    2015-04-01

    As glaciers are sensitive to local climate, their moraines position and ages are used to infer past climates and glacier dynamics. These chronologies are only valid if all dated moraines are formed as the result of climatically driven advance and subsequent retreat. Hence, any accurate palaeoenvironmental reconstruction requires thorough identification of the landform genesis by complex approach including geomorphological, sedimentological and structural landform investigation. Here are presented the implication of such approach for the reconstruction of the mega-hummocky deposits formation both of glacial and landslide origin in the glaciated Alai Valley of the Northern Pamir with further discussion on these and similar deposits validity for palaeoclimatic reconstructions. The Tibetan Plateau valleys are the largest glaciated regions beyond the ice sheets with high potential to provide the best geological record of glacial chronologies and, however, with higher probabilities of the numerous rock avalanche deposits including those that were initially considered of glacial origin (Hewitt, 1999). The Alai Valley is the largest intermountain depression in the upper reaches of the Amudarja River basin that has captured numerous unidentified extensive hummocky deposits descending from the Zaalai Range of Northern Pamir, covering area in more than 800 km2. Such vast hummocky deposits are usually could be formed either: 1) glacially by rapid glacial retreat due to the climate signal or triggered a-climatically glacial changes, such as glacial surge or landslide impact, or 2) during the landslide emplacement. Combination of sediment tests on agglomerates forming only in rock avalanche material (Reznichenko et al., 2012) and detailed geomorphological and sedimentological descriptions of these deposits allowed reconstructing the glacial deposition in the Koman and Lenin glacial catchments with identification of two gigantic rock avalanches and their relation to this glacial

  10. Effects of deposition temperature and ammonia flow on metal-organic chemical vapor deposition of hexagonal boron nitride

    NASA Astrophysics Data System (ADS)

    Rice, Anthony; Allerman, Andrew; Crawford, Mary; Beechem, Thomas; Ohta, Taisuke; Spataru, Catalin; Figiel, Jeffrey; Smith, Michael

    2018-03-01

    The use of metal-organic chemical vapor deposition at high temperature is investigated as a means to produce epitaxial hexagonal boron nitride (hBN) at the wafer scale. Several categories of hBN films were found to exist based upon precursor flows and deposition temperature. Low, intermediate, and high NH3 flow regimes were found to lead to fundamentally different deposition behaviors. The low NH3 flow regimes yielded discolored films of boron sub-nitride. The intermediate NH3 flow regime yielded stoichiometric films that could be deposited as thick films. The high NH3 flow regime yielded self-limited deposition with thicknesses limited to a few mono-layers. A Langmuir-Hinshelwood mechanism is proposed to explain the onset of self-limited behavior for the high NH3 flow regime. Photoluminescence characterization determined that the intermediate and high NH3 flow regimes could be further divided into low and high temperature behaviors with a boundary at 1500 °C. Films deposited with both high NH3 flow and high temperature exhibited room temperature free exciton emission at 210 nm and 215.9 nm.

  11. Thin Film Deposition Using Energetic Ions

    PubMed Central

    Manova, Darina; Gerlach, Jürgen W.; Mändl, Stephan

    2010-01-01

    One important recent trend in deposition technology is the continuous expansion of available processes towards higher ion assistance with the subsequent beneficial effects to film properties. Nowadays, a multitude of processes, including laser ablation and deposition, vacuum arc deposition, ion assisted deposition, high power impulse magnetron sputtering and plasma immersion ion implantation, are available. However, there are obstacles to overcome in all technologies, including line-of-sight processes, particle contaminations and low growth rates, which lead to ongoing process refinements and development of new methods. Concerning the deposited thin films, control of energetic ion bombardment leads to improved adhesion, reduced substrate temperatures, control of intrinsic stress within the films as well as adjustment of surface texture, phase formation and nanotopography. This review illustrates recent trends for both areas; plasma process and solid state surface processes. PMID:28883323

  12. Increasing aeolian dust deposition to snowpacks in the Rocky Mountains inferred from snowpack, wet deposition, and aerosol chemistry

    USGS Publications Warehouse

    Clow, David W.; Williams, Mark W.; Schuster, Paul F.

    2016-01-01

    Mountain snowpacks are a vital natural resource for ∼1.5 billion people in the northern Hemisphere, helping to meet human and ecological demand for water in excess of that provided by summer rain. Springtime warming and aeolian dust deposition accelerate snowmelt, increasing the risk of water shortages during late summer, when demand is greatest. While climate networks provide data that can be used to evaluate the effect of warming on snowpack resources, there are no established regional networks for monitoring aeolian dust deposition to snow. In this study, we test the hypothesis that chemistry of snow, wet deposition, and aerosols can be used as a surrogate for dust deposition to snow. We then analyze spatial patterns and temporal trends in inferred springtime dust deposition to snow across the Rocky Mountains, USA, for 1993–2014. Geochemical evidence, including strong correlations (r2 ≥ 0.94) between Ca2+, alkalinity, and dust concentrations in snow deposited during dust events, indicate that carbonate minerals in dust impart a strong chemical signature that can be used to track dust deposition to snow. Spatial patterns in chemistry of snow, wet deposition, and aerosols indicate that dust deposition increases from north to south in the Rocky Mountains, and temporal trends indicate that winter/spring dust deposition increased by 81% in the southern Rockies during 1993–2014. Using a multivariate modeling approach, we determined that increases in dust deposition and decreases in springtime snowfall combined to accelerate snowmelt timing in the southern Rockies by approximately 7–18 days between 1993 and 2014. Previous studies have shown that aeolian dust emissions may have doubled globally during the 20th century, possibly due to drought and land-use change. Climate projections for increased aridity in the southwestern U.S., northern Africa, and other mid-latitude regions of the northern Hemisphere suggest that aeolian dust emissions may continue to

  13. Mercury from mineral deposits and potential environmental impact

    USGS Publications Warehouse

    Rytuba, J.J.

    2003-01-01

    Mercury deposits are globally distributed in 26 mercury mineral belts. Three types of mercury deposits occur in these belts: silica-carbonate, hot-spring, and Almaden. Mercury is also produced as a by-product from several types of gold-silver and massive sulfide deposits, which account for 5% of the world's production. Other types of mineral deposits can be enriched in mercury and mercury phases present are dependent on deposit type. During processing of mercury ores, secondary mercury phases form and accumulate in mine wastes. These phases are more soluble than cinnabar, the primary ore mineral, and cause mercury deposits to impact the environment more so than other types of ore deposits enriched in mercury. Release and transport of mercury from mine wastes occur primarily as mercury-enriched particles and colloids. Production from mercury deposits has decreased because of environmental concerns, but by-product production from other mercury-enriched mineral deposits remains important.

  14. 27 CFR 53.157 - Deposit requirement for deposits made for calendar quarters prior to July 1, 1995.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... calendar quarter, the person deposits any underpayment for the month by the 9th day of the second month... quarter, the person deposits any underpayment for such month by the 9th day of the second month following... month in a calendar quarter, the person deposits any underpayment for such month by the 9th day of the...

  15. The quantitative determination of calcite associated with the carbonate-bearing apatites

    USGS Publications Warehouse

    Silverman, Sol R.; Fuyat, Ruth K.; Weiser, Jeanne D.

    1951-01-01

    The CO2 combined as calcite in carbonate-bearing apatites as been distinguished from that combined as carbonate-apatite, or present in some form other than calcite, by use of X-ray powder patterns, differential thermal analyses, and differential solubility tests. These methods were applied to several pure apatite minerals, to one fossil bone, and to a group of phosphorites from the Phosphoria formation of Permian age from Trail Canyon and the Conda mine, Idaho, and the Laketown district, Utah. With the exceptions of pure fluorapatite, pure carbonate-flueorapatite, and one phosphorite from Trail Canyon, these substances contain varying amounts of calcite, but in all the samples an appreciable part of the carbonite content is not present as calcite. The results of solubility tests, in which the particle size of sample and the length of solution time were varied, imply that the carbonate content is not due to shielded calcite entrapped along an internal network of surfaces.

  16. MODELING DEPOSITION OF INHALED PARTICLES

    EPA Science Inventory

    Modeling Deposition of Inhaled Particles: ABSTRACT

    The mathematical modeling of the deposition and distribution of inhaled aerosols within human lungs is an invaluable tool in predicting both the health risks associated with inhaled environmental aerosols and the therapeut...

  17. Phanerozoic Rifting Phases And Mineral Deposits

    NASA Astrophysics Data System (ADS)

    Hassaan, Mahmoud

    2016-04-01

    In North Africa occur Mediterranean and Red Sea metallogenic provinces. In each province distribute 47 iron- manganese- barite and lead-zinc deposits with tectonic-structural control. The author presents in this paper aspects of position of these deposits in the two provinces with Phanerozoic rifting . The Mediterranean Province belongs to two epochs, Hercynian and Alpine. The Hercynian Epoch manganese deposits in only Moroccoa- Algeria belong to Paleozoic tectonic zones and Proterozoic volcanics. The Alpine Epoch iron-manganese deposits are of post-orogenic exhalative-sedimentary origin. Manganese deposits in southern Morocco occur in Kabil-Rief quartz-chalcedony veins controlled by faults in andesitic sheets and in bedded pelitic tuffs, strata-form lenses and ore veins, in Precambrian schist and in Triassic and Cretaceous dolomites. Disseminated manganese with quartz and barite and effusive hydrothermal veins are hosted in Paleocene volcanics. Manganese deposits in Algeria are limited and unrecorded in Tunisia. Strata-form iron deposits in Atlas Heights are widespread in sub-rift zone among Jurassic sediments inter-bedding volcanic rocks. In Algeria, Group Beni-Saf iron deposits are localized along the Mediterranean coast in terrigenous and carbonate rocks of Jurassic, Cretaceous and Eocene age within faults and bedding planes. In Morocco strata-form hydrothermal lead-zinc deposits occur in contact zone of Tertiary andesite inter-bedding Cambrian shale, Lias dolomites and Eocene andesite. In both Algeria and Tunisia metasomatic Pb-Zn veins occur in Campanian - Maastrichtian carbonates, Triassic breccia, Jurassic limestone, Paleocene sandstones and limestone and Neogene conglomerates and sandstones. The Red Sea metallogenic province belongs to the Late Tertiary-Miocene times. In Wadi Araba hydrothermal iron-manganese deposits occur in Cretaceous sediments within 320°and 310 NW faults related to Tertiary basalt. Um-Bogma iron-manganese deposits are closely

  18. Chemistry of Non-Equilibrium Film Deposition.

    DTIC Science & Technology

    1985-12-01

    titanium isopropoxide mixed with water solutions of lanthanum and lead nitrate. The gels were dehydrated, then fired to 600C to remove all organics...OW- ’so IRO $Va. ame Thin films; titanium dioxide; -PuZT,- ion beam deposition; annealing,’ trnmiso electron microscopy. 4 - . - S \\AISST 0A ZT *Can...Deposition....... . ... *.... .. ... .. ..... .. . .... 2 C. Nonequilibrium Physical Deposition.................... 3 1. Titanium Oxide Films

  19. Electrochemical deposited nickel nanowires: influence of deposition bath temperature on the morphology and physical properties

    NASA Astrophysics Data System (ADS)

    Sofiah, A. G. N.; Kananathan, J.; Samykano, M.; Ulakanathan, S.; Lah, N. A. C.; Harun, W. S. W.; Sudhakar, K.; Kadirgama, K.; Ngui, W. K.; Siregar, J. P.

    2017-10-01

    This paper investigates the influence of the electrolytic bath temperature on the morphology and physical properties of nickel (Ni) nanowires electrochemically deposited into the anodic alumina oxide porous membrane (AAO). The synthesis was performed using nickel sulfate hexahydrate (NiSO4.6H2O) and boric acid (H3BO3) as an electrolytic bath for the electrochemical deposition of Ni nanowires. During the experiment, the electrolyte bath temperature varied from 40°C, 80°C, and 120°C. After the electrochemical deposition process, AAO templates cleaned with distilled water preceding to dissolution in sodium hydroxide (NaOH) solution to obtain free-standing Ni nanowires. Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive Spectroscopy (EDX) and X-ray Diffraction (XRD) analysis were employed to characterize the morphology and physical properties of the synthesized Ni nanowires. Finding reveals the electrodeposition bath temperature significantly influences the morphology and physical properties of the synthesized Ni nanowires. Rougher surface texture, larger crystal size, and longer Ni nanowires obtained as the deposition bath temperature increased. From the physical properties properties analysis, it can be concluded that deposition bath temperature influence the physical properties of Ni nanowires.

  20. A special issue devoted to gold deposits in northern Nevada: Part 2. Carlin-type Deposits

    USGS Publications Warehouse

    Hofstra, Albert H.; John, David A.; Theodore, Ted G.

    2003-01-01

    Despite the similar age, tectonic setting, alteration types, mineral parageneses, and geochemical signatures of the deposits studied, these papers do not lead to consensus regarding genetic models for Carlin-type deposits. Rather, the separate investigations by different workers, utilizing both similar and unlike approaches, result in markedly different conclusions. Some of this disparity probably is due to real differences in the origin of different districts; however, the opposing conclusions arrived at by investigations on neighboring deposits in a single district are more problematic and most likely are due to difficulties resulting from the superposition of different types and ages of gold mineralization or to substantial variations in the hydrology and proportions of fluid components derived from deep and shallow sources in each deposit. Further work is needed to validate and understand the significance of these differences.

  1. The influence of spray properties on intranasal deposition.

    PubMed

    Foo, Mow Yee; Cheng, Yung-Sung; Su, Wei-Chung; Donovan, Maureen D

    2007-01-01

    While numerous devices, formulations, and spray characteristics have been shown to influence nasal deposition efficiency, few studies have attempted to identify which of these interacting factors plays the greatest role in nasal spray deposition. The deposition patterns of solutions with a wide range of surface tensions and viscosities were measured using an MRI-derived nasal cavity replica. The resulting spray plumes had angles between 29 degrees and 80 degrees and contained droplet sizes (D(v50)) from 37-157 microm. Each formulation contained rhodamine 590 as a fluorescent marker for detection. Administration angles of 30 degrees , 40 degrees , or 50 degrees above horizontal were tested to investigate the role of user technique on nasal deposition. The amount of spray deposited within specific regions of the nasal cavity was determined by disassembling the replica and measuring the amount of rhodamine retained in each section. Most of the spray droplets were deposited onto the anterior region of the model, but sprays with small plume angles were capable of reaching the turbinate region with deposition efficiencies approaching 90%. Minimal dependence on droplet size, viscosity, or device was observed. Changes in inspiratory flow rate (0-60 L/min) had no significant effect on turbinate deposition efficiency. Both plume angle and administration angle were found to be important factors in determining deposition efficiency. For administration angles of 40 degrees or 50 degrees , maximal turbinate deposition efficiency (30-50%) occurred with plume angles of 55-65 degrees , whereas a 30 degrees administration angle gave an approximately 75% deposition efficiency for similar plume angles. Deposition efficiencies of approximately 90% could be achieved with plume angles <30 degrees using 30 degrees administration angles. Both the plume angle and administration angle are critical factors in determining deposition efficiency, while many other spray parameters, including

  2. SnS thin films deposited by chemical bath deposition, dip coating and SILAR techniques

    NASA Astrophysics Data System (ADS)

    Chaki, Sunil H.; Chaudhary, Mahesh D.; Deshpande, M. P.

    2016-05-01

    The SnS thin films were synthesized by chemical bath deposition (CBD), dip coating and successive ionic layer adsorption and reaction (SILAR) techniques. In them, the CBD thin films were deposited at two temperatures: ambient and 70 °C. The energy dispersive analysis of X-rays (EDAX), X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM) and optical spectroscopy techniques were used to characterize the thin films. The electrical transport properties studies on the as-deposited thin films were done by measuring the I-V characteristics, DC electrical resistivity variation with temperature and the room temperature Hall effect. The obtained results are deliberated in this paper.

  3. Physical vapor deposition and metalorganic chemical vapor deposition of yttria-stabilized zirconia thin films

    NASA Astrophysics Data System (ADS)

    Kaufman, David Y.

    Two vapor deposition techniques, dual magnetron oblique sputtering (DMOS) and metalorganic chemical vapor deposition (MOCVD), have been developed to produce yttria-stabilized zirconia (YSZ) films with unique microstructures. In particular, biaxially textured thin films on amorphous substrates and dense thin films on porous substrates have been fabricated by DMOS and MOCVD, respectively. DMOS YSZ thin films were deposited by reactive sputtering onto Si (native oxide surface) substrates positioned equidistant between two magnetron sources such that the fluxes arrived at oblique angles with respect to the substrate normal. Incident fluxes from two complimentary oblique directions were necessary for the development of biaxial texture. The films displayed a strong [001] out-of-plane orientation with the <110> direction in the film aligned with the incident flux. Biaxial texture improved with increasing oblique angle and film thickness, and was stronger for films deposited with Ne than with Ar. The films displayed a columnar microstructure with grain bundling perpendicular to the projected flux direction, the degree of which increased with oblique angle and thickness. The texture decreased by sputtering at pressures at which the flux of sputtered atoms was thermalized. These results suggested that grain alignment is due to directed impingement of both sputtered atoms and reflected energetic neutrals. The best texture, a {111} phi FWHM of 23°, was obtained in a 4.8 mum thick film deposited at an oblique angle of 56°. MOCVD YSZ thin films were deposited in a vertical cold-wall reactor using Zr(tmhd)4 and Y(tmhd)3 precursors. Fully stabilized YSZ films with 9 mol% could be deposited by controlling the bubbler temperatures. YSZ films on Si substrates displayed a transition at 525°C from surface kinetic limited growth, with an activation energy of 5.5 kJ/mole, to mass transport limited growth. Modifying the reactor by lowering the inlet height and introducing an Ar baffle

  4. The Pulsed Cylindrical Magnetron for Deposition

    NASA Astrophysics Data System (ADS)

    Korenev, Sergey

    2012-10-01

    The magnetron sputtering deposition of films and coatings broadly uses in microelectronics, material science, environmental applications and etc. The rate of target evaporation and time for deposition of films and coatings depends on magnetic field. These parameters link with efficiency of gas molecules ionization by electrons. The cylindrical magnetrons use for deposition of films and coatings on inside of pipes for different protective films and coatings in oil, chemical, environmental applications. The classical forming of magnetic field by permanent magnets or coils for big and long cylindrical magnetrons is complicated. The new concept of pulsed cylindrical magnetron for high rate deposition of films and coating for big and long pipes is presented in this paper. The proposed cylindrical magnetron has azimuthally pulsed high magnetic field, which allows forming the high ionized plasma and receiving high rate of evaporation material of target (central electrode). The structure of proposed pulsed cylindrical magnetron sputtering system is given. The main requirements to deposition system are presented. The preliminary data for forming of plasma and deposition of Ta films and coatings on the metal pipers are discussed. The comparison of classical and proposed cylindrical magnetrons is given. The analysis of potential applications is considered.

  5. 7 CFR 1.148 - Depositions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... (telephone, audio-visual telecommunication, or personal attendance of those who are to participate in the... that conducting the deposition by audio-visual telecommunication: (i) Is necessary to prevent prejudice... determines that a deposition conducted by audio-visual telecommunication would measurably increase the United...

  6. Hybrid inorganic–organic superlattice structures with atomic layer deposition/molecular layer deposition

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

    Tynell, Tommi; Yamauchi, Hisao; Karppinen, Maarit, E-mail: maarit.karppinen@aalto.fi

    2014-01-15

    A combination of the atomic layer deposition (ALD) and molecular layer deposition (MLD) techniques is successfully employed to fabricate thin films incorporating superlattice structures that consist of single layers of organic molecules between thicker layers of ZnO. Diethyl zinc and water are used as precursors for the deposition of ZnO by ALD, while three different organic precursors are investigated for the MLD part: hydroquinone, 4-aminophenol and 4,4′-oxydianiline. The successful superlattice formation with all the organic precursors is verified through x-ray reflectivity studies. The effects of the interspersed organic layers/superlattice structure on the electrical and thermoelectric properties of ZnO are investigatedmore » through resistivity and Seebeck coefficient measurements at room temperature. The results suggest an increase in carrier concentration for small concentrations of organic layers, while higher concentrations seem to lead to rather large reductions in carrier concentration.« less

  7. Improvements in Ionized Cluster-Beam Deposition

    NASA Technical Reports Server (NTRS)

    Fitzgerald, D. J.; Compton, L. E.; Pawlik, E. V.

    1986-01-01

    Lower temperatures result in higher purity and fewer equipment problems. In cluster-beam deposition, clusters of atoms formed by adiabatic expansion nozzle and with proper nozzle design, expanding vapor cools sufficiently to become supersaturated and form clusters of material deposited. Clusters are ionized and accelerated in electric field and then impacted on substrate where films form. Improved cluster-beam technique useful for deposition of refractory metals.

  8. Dry deposition of gaseous oxidized mercury in Western Maryland.

    PubMed

    Castro, Mark S; Moore, Chris; Sherwell, John; Brooks, Steve B

    2012-02-15

    The purpose of this study was to directly measure the dry deposition of gaseous oxidized mercury (GOM) in western Maryland. Annual estimates were made using passive ion-exchange surrogate surfaces and a resistance model. Surrogate surfaces were deployed for seventeen weekly sampling periods between September 2009 and October 2010. Dry deposition rates from surrogate surfaces ranged from 80 to 1512 pgm(-2)h(-1). GOM dry deposition rates were strongly correlated (r(2)=0.75) with the weekly average atmospheric GOM concentrations, which ranged from 2.3 to 34.1 pgm(-3). Dry deposition of GOM could be predicted from the ambient air concentrations of GOM using this equation: GOM dry deposition (pgm(-2)h(-1))=43.2 × GOM concentration-80.3. Dry deposition velocities computed using GOM concentrations and surrogate surface GOM dry deposition rates, ranged from 0.2 to 1.7 cms(-1). Modeled dry deposition rates were highly correlated (r(2)=0.80) with surrogate surface dry deposition rates. Using the overall weekly average surrogate surface dry deposition rate (369 ± 340 pg m(-2)h(-1)), we estimated an annual GOM dry deposition rate of 3.2 μg m(-2)year(-1). Using the resistance model, we estimated an annual GOM dry deposition rate of 3.5 μg m(-2)year(-1). Our annual GOM dry deposition rates were similar to the dry deposition (3.3 μg m(-2)h(-1)) of gaseous elemental mercury (GEM) at our site. In addition, annual GOM dry deposition was approximately 1/2 of the average annual wet deposition of total mercury (7.7 ± 1.9 μg m(-2)year(-1)) at our site. Total annual mercury deposition from dry deposition of GOM and GEM and wet deposition was approximately 14.4 μg m(-2)year(-1), which was similar to the average annual litterfall deposition (15 ± 2.1 μg m(-2)year(-1)) of mercury, which was also measured at our site. Copyright © 2012 Elsevier B.V. All rights reserved.

  9. The Myszkow porphyry copper-molybdenum deposit, Poland

    USGS Publications Warehouse

    Chaffee, M.A.; Eppinger, R.G.; Lason, K.; Slosarz, J.; Podemski, M.

    1994-01-01

    The porphyry copper-molybdenum deposit at Myszkow, south-central Poland, lies in the Cracow-Silesian orogenic belt, in the vicinity of a Paleozoic boundary between two tectonic plates. The deposit is hosted in a complex that includes early Paleozoic metasedimentary rocks intruded in the late Paleozoic by a predominantly granodioritic pluton. This deposit exhibits many features that are typical of porphyry copper deposits associated with calc-alkaline intrusive rocks, including ore- and alteration-mineral suites, zoning of ore and alteration minerals, fluid-inclusion chemistry, tectonic setting, and structural style of veining. Unusual features of the Myszkow deposit include high concentrations of tungsten and the late Paleozoic (Variscan) age. -Authors

  10. Progress in the Study of Coastal Storm Deposits

    NASA Astrophysics Data System (ADS)

    Xiong, Haixian; Huang, Guangqing; Fu, Shuqing; Qian, Peng

    2018-05-01

    Numerous studies have been carried out to identify storm deposits and decipher storm-induced sedimentary processes in coastal and shallow-marine areas. This study aims to provide an in-depth review on the study of coastal storm deposits from the following five aspects. 1) The formation of storm deposits is a function of hydrodynamic and sedimentary processes under the constraints of local geological and ecological factors. Many questions remain to demonstrate the genetic links between storm-related processes and a variety of resulting deposits such as overwash deposits, underwater deposits and hummocky cross-stratification (HCS). Future research into the formation of storm deposits should combine flume experiments, field observations and numerical simulations, and make full use of sediment source tracing methods. 2) Recently there has been rapid growth in the number of studies utilizing sediment provenance analysis to investigate the source of storm deposits. The development of source tracing techniques, such as mineral composition, magnetic susceptibility, microfossil and geochemical property, has allowed for better understanding of the depositional processes and environmental changes associated with coastal storms. 3) The role of extreme storms in the sedimentation of low-lying coastal wetlands with diverse ecosystem services has also drawn a great deal of attention. Many investigations have attempted to quantify widespread land loss, vertical marsh sediment accumulation and wetland elevation change induced by major hurricanes. 4) Paleostorm reconstructions based on storm sedimentary proxies have shown many advantages over the instrumental records and historic documents as they allow for the reconstruction of storm activities on millennial or longer time scales. Storm deposits having been used to establish proxies mainly include beach ridges and shelly cheniers, coral reefs, estuary-deltaic storm sequences and overwash deposits. Particularly over the past few

  11. 46 CFR 502.204 - Depositions upon written interrogatories.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 9 2011-10-01 2011-10-01 false Depositions upon written interrogatories. 502.204... PRACTICE AND PROCEDURE Depositions, Written Interrogatories, and Discovery § 502.204 Depositions upon written interrogatories. (a) Serving interrogatories; notice. A party desiring to take the deposition of...

  12. 46 CFR 502.204 - Depositions upon written interrogatories.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 9 2010-10-01 2010-10-01 false Depositions upon written interrogatories. 502.204... PRACTICE AND PROCEDURE Depositions, Written Interrogatories, and Discovery § 502.204 Depositions upon written interrogatories. (a) Serving interrogatories; notice. A party desiring to take the deposition of...

  13. ATMOSPHERIC DEPOSITION MODELING AND MONITORING OF NUTRIENTS

    EPA Science Inventory

    This talk presents an overview of the capabilities and roles that regional atmospheric deposition models can play with respect to multi-media environmental problems. The focus is on nutrient deposition (nitrogen). Atmospheric deposition of nitrogen is an important contributor to...

  14. Atomic layer deposition of copper thin film and feasibility of deposition on inner walls of waveguides

    NASA Astrophysics Data System (ADS)

    Yuqing, XIONG; Hengjiao, GAO; Ni, REN; Zhongwei, LIU

    2018-03-01

    Copper thin films were deposited by plasma-enhanced atomic layer deposition at low temperature, using copper(I)-N,N‧-di-sec-butylacetamidinate as a precursor and hydrogen as a reductive gas. The influence of temperature, plasma power, mode of plasma, and pulse time, on the deposition rate of copper thin film, the purity of the film and the step coverage were studied. The feasibility of copper film deposition on the inner wall of a carbon fibre reinforced plastic waveguide with high aspect ratio was also studied. The morphology and composition of the thin film were studied by atomic force microscopy and x-ray photoelectron spectroscopy, respectively. The square resistance of the thin film was also tested by a four-probe technique. On the basis of on-line diagnosis, a growth mechanism of copper thin film was put forward, and it was considered that surface functional group played an important role in the process of nucleation and in determining the properties of thin films. A high density of plasma and high free-radical content were helpful for the deposition of copper thin films.

  15. Ti-doped hydrogenated diamond like carbon coating deposited by hybrid physical vapor deposition and plasma enhanced chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Lee, Na Rae; Sle Jun, Yee; Moon, Kyoung Il; Sunyong Lee, Caroline

    2017-03-01

    Diamond-like carbon films containing titanium and hydrogen (Ti-doped DLC:H) were synthesized using a hybrid technique based on physical vapor deposition (PVD) and plasma enhanced chemical vapor deposition (PECVD). The film was deposited under a mixture of argon (Ar) and acetylene gas (C2H2). The amount of Ti in the Ti-doped DLC:H film was controlled by varying the DC power of the Ti sputtering target ranging from 0 to 240 W. The composition, microstructure, mechanical and chemical properties of Ti-doped DLC:H films with varying Ti concentrations, were investigated using Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), nano indentation, a ball-on-disk tribometer, a four-point probe system and dynamic anodic testing. As a result, the optimum composition of Ti in Ti-doped DLC:H film using our hybrid method was found to be a Ti content of 18 at. %, having superior electrical conductivity and high corrosion resistance, suitable for bipolar plates. Its hardness value was measured to be 25.6 GPa with a low friction factor.

  16. Atmospheric nitrogen deposition in south-east Scotland: Quantification of the organic nitrogen fraction in wet, dry and bulk deposition

    NASA Astrophysics Data System (ADS)

    González Benítez, Juan M.; Cape, J. Neil; Heal, Mathew R.; van Dijk, Netty; Díez, Alberto Vidal

    Water soluble organic nitrogen (WSON) compounds are ubiquitous in precipitation and in the planetary boundary layer, and therefore are a potential source of bioavailable reactive nitrogen. This paper examines weekly rain data over a period of 22 months from June 2005 to March 2007 collected in 2 types of rain collector (bulk deposition and "dry + wet" deposition) located in a semi-rural area 15 km southwest of Edinburgh, UK (N55°51'44″, W3°12'19″). Bulk deposition collectors are denoted in this paper as "standard rain gauges", and they are the design used in the UK national network for monitoring precipitation composition. "Dry + wet" deposition collectors are flushing rain gauges and they are equipped with a rain detector (conductivity array), a spray nozzle, a 2-way valve and two independent bottles to collect funnel washings (dry deposition) and true wet deposition. On average, for the 27 weekly samples with 3 valid replicates for the 2 types of collectors, dissolved organic nitrogen (DON) represented 23% of the total dissolved nitrogen (TDN) in bulk deposition. Dry deposition of particles and gas on the funnel surface, rather than rain, contributed over half of all N-containing species (inorganic and organic). Some discrepancies were found between bulk rain gauges and flushing rain gauges, for deposition of both TDN and DON, suggesting biological conversion and loss of inorganic N in the flushing samplers.

  17. Surface morphology of a modified ballistic deposition model.

    PubMed

    Banerjee, Kasturi; Shamanna, J; Ray, Subhankar

    2014-08-01

    The surface and bulk properties of a modified ballistic deposition model are investigated. The deposition rule interpolates between nearest- and next-nearest-neighbor ballistic deposition and the random deposition models. The stickiness of the depositing particle is controlled by a parameter and the type of interparticle force. Two such forces are considered: Coulomb and van der Waals type. The interface width shows three distinct growth regions before eventual saturation. The rate of growth depends more strongly on the stickiness parameter than on the type of interparticle force. However, the porosity of the deposits is strongly influenced by the interparticle force.

  18. Chemical-Vapor Deposition Of Silicon Carbide

    NASA Technical Reports Server (NTRS)

    Cagliostro, D. E.; Riccitiello, S. R.; Ren, J.; Zaghi, F.

    1993-01-01

    Report describes experiments in chemical-vapor deposition of silicon carbide by pyrolysis of dimethyldichlorosilane in hydrogen and argon carrier gases. Directed toward understanding chemical-kinetic and mass-transport phenomena affecting infiltration of reactants into, and deposition of SiC upon, fabrics. Part of continuing effort to develop method of efficient and more nearly uniform deposition of silicon carbide matrix throughout fabric piles to make improved fabric/SiC-matrix composite materials.

  19. Laser ablation and deposition of wide bandgap semiconductors: plasma and nanostructure of deposits diagnosis

    NASA Astrophysics Data System (ADS)

    Sanz, M.; López-Arias, M.; Rebollar, E.; de Nalda, R.; Castillejo, M.

    2011-12-01

    Nanostructured CdS and ZnS films on Si (100) substrates were obtained by nanosecond pulsed laser deposition at the wavelengths of 266 and 532 nm. The effect of laser irradiation wavelength on the surface structure and crystallinity of deposits was characterized, together with the composition, expansion dynamics and thermodynamic parameters of the ablation plume. Deposits were analyzed by environmental scanning electron microscopy, atomic force microscopy and X-ray diffraction, while in situ monitoring of the plume was carried out with spectral, temporal and spatial resolution by optical emission spectroscopy. The deposits consist of 25-50 nm nanoparticle assembled films but ablation in the visible results in larger aggregates (150 nm) over imposed on the film surface. The aggregate free films grown at 266 nm on heated substrates are thicker than those grown at room temperature and in the former case they reveal a crystalline structure congruent with that of the initial target material. The observed trends are discussed in reference to the light absorption step, the plasma composition and the nucleation processes occurring on the substrate.

  20. Modeling physical vapor deposition of energetic materials

    DOE PAGES

    Shirvan, Koroush; Forrest, Eric C.

    2018-03-28

    Morphology and microstructure of organic explosive films formed using physical vapor deposition (PVD) processes strongly depends on local surface temperature during deposition. Currently, there is no accurate means of quantifying the local surface temperature during PVD processes in the deposition chambers. This study focuses on using a multiphysics computational fluid dynamics tool, STARCCM+, to simulate pentaerythritol tetranitrate (PETN) deposition. The PETN vapor and solid phase were simulated using the volume of fluid method and its deposition in the vacuum chamber on spinning silicon wafers was modeled. The model also included the spinning copper cooling block where the wafers are placedmore » along with the chiller operating with forced convection refrigerant. Implicit time-dependent simulations in two- and three-dimensional were performed to derive insights in the governing physics for PETN thin film formation. PETN is deposited at the rate of 14 nm/s at 142.9 °C on a wafer with an initial temperature of 22 °C. The deposition of PETN on the wafers was calculated at an assumed heat transfer coefficient (HTC) of 400 W/m 2 K. This HTC proved to be the most sensitive parameter in determining the local surface temperature during deposition. Previous experimental work found noticeable microstructural changes with 0.5 mm fused silica wafers in place of silicon during the PETN deposition. This work showed that fused silica slows initial wafer cool down and results in ~10 °C difference for the surface temperature at 500 μm PETN film thickness. It was also found that the deposition surface temperature is insensitive to the cooling power of the copper block due to the copper block's very large heat capacity and thermal conductivity relative to the heat input from the PVD process. Future work should incorporate the addition of local stress during PETN deposition. Lastly, based on simulation results, it is also recommended to investigate the impact of wafer

  1. Modeling physical vapor deposition of energetic materials

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

    Shirvan, Koroush; Forrest, Eric C.

    Morphology and microstructure of organic explosive films formed using physical vapor deposition (PVD) processes strongly depends on local surface temperature during deposition. Currently, there is no accurate means of quantifying the local surface temperature during PVD processes in the deposition chambers. This study focuses on using a multiphysics computational fluid dynamics tool, STARCCM+, to simulate pentaerythritol tetranitrate (PETN) deposition. The PETN vapor and solid phase were simulated using the volume of fluid method and its deposition in the vacuum chamber on spinning silicon wafers was modeled. The model also included the spinning copper cooling block where the wafers are placedmore » along with the chiller operating with forced convection refrigerant. Implicit time-dependent simulations in two- and three-dimensional were performed to derive insights in the governing physics for PETN thin film formation. PETN is deposited at the rate of 14 nm/s at 142.9 °C on a wafer with an initial temperature of 22 °C. The deposition of PETN on the wafers was calculated at an assumed heat transfer coefficient (HTC) of 400 W/m 2 K. This HTC proved to be the most sensitive parameter in determining the local surface temperature during deposition. Previous experimental work found noticeable microstructural changes with 0.5 mm fused silica wafers in place of silicon during the PETN deposition. This work showed that fused silica slows initial wafer cool down and results in ~10 °C difference for the surface temperature at 500 μm PETN film thickness. It was also found that the deposition surface temperature is insensitive to the cooling power of the copper block due to the copper block's very large heat capacity and thermal conductivity relative to the heat input from the PVD process. Future work should incorporate the addition of local stress during PETN deposition. Lastly, based on simulation results, it is also recommended to investigate the impact of wafer

  2. Vapor deposition routes to conformal polymer thin films

    PubMed Central

    Moni, Priya; Al-Obeidi, Ahmed

    2017-01-01

    Vapor phase syntheses, including parylene chemical vapor deposition (CVD) and initiated CVD, enable the deposition of conformal polymer thin films to benefit a diverse array of applications. This short review for nanotechnologists, including those new to vapor deposition methods, covers the basic theory in designing a conformal polymer film vapor deposition, sample preparation and imaging techniques to assess film conformality, and several applications that have benefited from vapor deposited, conformal polymer thin films. PMID:28487816

  3. Thermal release of D2 from new Be-D co-deposits on previously baked co-deposits

    NASA Astrophysics Data System (ADS)

    Baldwin, M. J.; Doerner, R. P.

    2015-12-01

    Past experiments and modeling with the TMAP code in [1, 2] indicated that Be-D co-deposited layers are less (time-wise) efficiently desorbed of retained D in a fixed low-temperature bake, as the layer grows in thickness. In ITER, beryllium rich co-deposited layers will grow in thickness over the life of the machine. Although, compared with the analyses in [1, 2], ITER presents a slightly different bake efficiency problem because of instances of prior tritium recover/control baking. More relevant to ITER, is the thermal release from a new and saturated co-deposit layer in contact with a thickness of previously-baked, less-saturated, co-deposit. Experiments that examine the desorption of saturated co-deposited over-layers in contact with previously baked under-layers are reported and comparison is made to layers of the same combined thickness. Deposition temperatures of ∼323 K and ∼373 K are explored. It is found that an instance of prior bake leads to a subtle effect on the under-layer. The effect causes the thermal desorption of the new saturated over-layer to deviate from the prediction of the validated TMAP model in [2]. Instead of the D thermal release reflecting the combined thickness and levels of D saturation in the over and under layer, experiment differs in that, i) the desorption is a fractional superposition of desorption from the saturated over-layer, with ii) that of the combined over and under -layer thickness. The result is not easily modeled by TMAP without the incorporation of a thin BeO inter-layer which is confirmed experimentally on baked Be-D co-deposits using X-ray micro-analysis.

  4. The zeolite deposits of Greece

    USGS Publications Warehouse

    Stamatakis, M.G.; Hall, A.; Hein, J.R.

    1996-01-01

    Zeolites are present in altered pyroclastic rocks at many localities in Greece, and large deposits of potential economic interest are present in three areas: (1) the Evros region of the province of Thrace in the north-eastern part of the Greek mainland; (2) the islands of Kimolos and Poliegos in the western Aegean; and (3) the island of Samos in the eastern Aegean Sea. The deposits in Thrace are of Eocene-Oligocene age and are rich in heulandite and/or clinoptilolite. Those of Kimolos and Poliegos are mainly Quaternary and are rich in mordenite. Those of Samos are Miocene, and are rich in clinoptilolite and/or analcime. The deposits in Thrace are believed to have formed in an open hydrological system by the action of meteoric water, and those of the western Aegean islands in a similar way but under conditions of high heat flow, whereas the deposits in Samos were formed in a saline-alkaline lake.

  5. Massive CO2 Ice Deposits Sequestered in the South Polar Layered Deposits of Mars

    USGS Publications Warehouse

    Phillips, Roger J.; Davis, Brian J.; Tanaka, Kenneth L.; Byrne, Shane; Mellon, Michael T.; Putzig, Nathaniel E.; Haberle, Robert M.; Kahre, Melinda A.; Campbell, Bruce A.; Carter, Lynn M.; Smith, Isaac B.; Holt, John W.; Smrekar, Suzanne E.; Nunes, Daniel C.; Plaut, Jeffrey J.; Egan, Anthony F.; Titus, Timothy N.; Seu, Roberto

    2011-01-01

    Shallow Radar soundings from the Mars Reconnaissance Orbiter reveal a buried deposit of carbon dioxide (CO2) ice within the south polar layered deposits of Mars with a volume of 9500 to 12,500 cubic kilometers, about 30 times that previously estimated for the south pole residual cap. The deposit occurs within a stratigraphic unit that is uniquely marked by collapse features and other evidence of interior CO2 volatile release. If released into the atmosphere at times of high obliquity, the CO2 reservoir would increase the atmospheric mass by up to 80%, leading to more frequent and intense dust storms and to more regions where liquid water could persist without boiling.

  6. CORRECTION FACTORS FOR COVARIANCE BETWEEN CONCENTRATION AND DEPOSITION VELOCITY ON CASTNET HNO3 DEPOSITION ESTIMATES

    EPA Science Inventory

    The covariance between hourly concentration (C) and deposition velocity (V) for various atmospheric; species may act to bias the, deposition (D) computed from the product of the weekly average C and 'V. This is a potential problem for the CASTNet filter pack (FP) species, nitric...

  7. Assessment of Global Mercury Deposition through Litterfall.

    PubMed

    Wang, Xun; Bao, Zhengduo; Lin, Che-Jen; Yuan, Wei; Feng, Xinbin

    2016-08-16

    There is a large uncertainty in the estimate of global dry deposition of atmospheric mercury (Hg). Hg deposition through litterfall represents an important input to terrestrial forest ecosystems via cumulative uptake of atmospheric Hg (most Hg(0)) to foliage. In this study, we estimate the quantity of global Hg deposition through litterfall using statistical modeling (Monte Carlo simulation) of published data sets of litterfall biomass production, tree density, and Hg concentration in litter samples. On the basis of the model results, the global annual Hg deposition through litterfall is estimated to be 1180 ± 710 Mg yr(-1), more than two times greater than the estimate by GEOS-Chem. Spatial distribution of Hg deposition through litterfall suggests that deposition flux decreases spatially from tropical to temperate and boreal regions. Approximately 70% of global Hg(0) dry deposition occurs in the tropical and subtropical regions. A major source of uncertainty in this study is the heterogeneous geospatial distribution of available data. More observational data in regions (Southeast Asia, Africa, and South America) where few data sets exist will greatly improve the accuracy of the current estimate. Given that the quantity of global Hg deposition via litterfall is typically 2-6 times higher than Hg(0) evasion from forest floor, global forest ecosystems represent a strong Hg(0) sink.

  8. 17 CFR 201.233 - Depositions upon oral examination.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 17 Commodity and Securities Exchanges 2 2010-04-01 2010-04-01 false Depositions upon oral... RULES OF PRACTICE Rules of Practice Initiation of Proceedings and Prehearing Rules § 201.233 Depositions... deposition shall make a written motion setting forth the reasons why such deposition should be taken...

  9. 46 CFR 502.203 - Depositions upon oral examination.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 9 2010-10-01 2010-10-01 false Depositions upon oral examination. 502.203 Section 502... PROCEDURE Depositions, Written Interrogatories, and Discovery § 502.203 Depositions upon oral examination. (a) Notice of examination. (1) A party desiring to take the deposition of any person upon oral...

  10. 17 CFR 201.233 - Depositions upon oral examination.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 17 Commodity and Securities Exchanges 2 2011-04-01 2011-04-01 false Depositions upon oral... RULES OF PRACTICE Rules of Practice Initiation of Proceedings and Prehearing Rules § 201.233 Depositions... deposition shall make a written motion setting forth the reasons why such deposition should be taken...

  11. 46 CFR 502.203 - Depositions upon oral examination.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 9 2011-10-01 2011-10-01 false Depositions upon oral examination. 502.203 Section 502... PROCEDURE Depositions, Written Interrogatories, and Discovery § 502.203 Depositions upon oral examination. (a) Notice of examination. (1) A party desiring to take the deposition of any person upon oral...

  12. 12 CFR 390.296 - Money Market Deposit Accounts.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 12 Banks and Banking 5 2013-01-01 2013-01-01 false Money Market Deposit Accounts. 390.296 Section 390.296 Banks and Banking FEDERAL DEPOSIT INSURANCE CORPORATION REGULATIONS AND STATEMENTS OF GENERAL... Affecting All State Savings Associations § 390.296 Money Market Deposit Accounts. (a) Money Market Deposit...

  13. 12 CFR 390.296 - Money Market Deposit Accounts.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 12 Banks and Banking 5 2012-01-01 2012-01-01 false Money Market Deposit Accounts. 390.296 Section 390.296 Banks and Banking FEDERAL DEPOSIT INSURANCE CORPORATION REGULATIONS AND STATEMENTS OF GENERAL... Affecting All State Savings Associations § 390.296 Money Market Deposit Accounts. (a) Money Market Deposit...

  14. 12 CFR 390.296 - Money Market Deposit Accounts.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 12 Banks and Banking 5 2014-01-01 2014-01-01 false Money Market Deposit Accounts. 390.296 Section 390.296 Banks and Banking FEDERAL DEPOSIT INSURANCE CORPORATION REGULATIONS AND STATEMENTS OF GENERAL... Affecting All State Savings Associations § 390.296 Money Market Deposit Accounts. (a) Money Market Deposit...

  15. Method and apparatus for removing and preventing window deposition during photochemical vapor deposition (photo-CVD) processes

    DOEpatents

    Tsuo, S.; Langford, A.A.

    1989-03-28

    Unwanted build-up of the film deposited on the transparent light-transmitting window of a photochemical vacuum deposition (photo-CVD) chamber is eliminated by flowing an etchant into the part of the photolysis region in the chamber immediately adjacent the window and remote from the substrate and from the process gas inlet. The respective flows of the etchant and the process gas are balanced to confine the etchant reaction to the part of the photolysis region proximate to the window and remote from the substrate. The etchant is preferably one that etches film deposit on the window, does not etch or affect the window itself, and does not produce reaction by-products that are deleterious to either the desired film deposited on the substrate or to the photolysis reaction adjacent the substrate. 3 figs.

  16. Method and apparatus for removing and preventing window deposition during photochemical vapor deposition (photo-CVD) processes

    DOEpatents

    Tsuo, Simon; Langford, Alison A.

    1989-01-01

    Unwanted build-up of the film deposited on the transparent light-transmitting window of a photochemical vacuum deposition (photo-CVD) chamber is eliminated by flowing an etchant into the part of the photolysis region in the chamber immediately adjacent the window and remote from the substrate and from the process gas inlet. The respective flows of the etchant and the process gas are balanced to confine the etchant reaction to the part of the photolysis region proximate to the window and remote from the substrate. The etchant is preferably one that etches film deposit on the window, does not etch or affect the window itself, and does not produce reaction by-products that are deleterious to either the desired film deposited on the substrate or to the photolysis reaction adjacent the substrate.

  17. 10 CFR 590.307 - Depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 4 2010-01-01 2010-01-01 false Depositions. 590.307 Section 590.307 Energy DEPARTMENT OF ENERGY (CONTINUED) NATURAL GAS (ECONOMIC REGULATORY ADMINISTRATION) ADMINISTRATIVE PROCEDURES WITH RESPECT TO THE IMPORT AND EXPORT OF NATURAL GAS Procedures § 590.307 Depositions. (a) Upon motion filed by...

  18. 49 CFR 821.19 - Depositions and other discovery.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 7 2011-10-01 2011-10-01 false Depositions and other discovery. 821.19 Section... Depositions and other discovery. (a) Depositions. After a petition for review or a complaint is filed, any party may take the testimony of any person, including a party, by deposition, upon oral examination or...

  19. 37 CFR 2.124 - Depositions upon written questions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2011-07-01 2011-07-01 false Depositions upon written... Depositions upon written questions. (a) A deposition upon written questions may be taken before any person before whom depositions may be taken as provided by Rule 28 of the Federal Rules of Civil Procedure. (b...

  20. 49 CFR 821.19 - Depositions and other discovery.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 49 Transportation 7 2010-10-01 2010-10-01 false Depositions and other discovery. 821.19 Section... Depositions and other discovery. (a) Depositions. After a petition for review or a complaint is filed, any party may take the testimony of any person, including a party, by deposition, upon oral examination or...

  1. 37 CFR 2.124 - Depositions upon written questions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2010-07-01 2010-07-01 false Depositions upon written... Depositions upon written questions. (a) A deposition upon written questions may be taken before any person before whom depositions may be taken as provided by Rule 28 of the Federal Rules of Civil Procedure. (b...

  2. 4 CFR 28.44 - Taking of depositions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 4 Accounts 1 2010-01-01 2010-01-01 false Taking of depositions. 28.44 Section 28.44 Accounts GOVERNMENT ACCOUNTABILITY OFFICE GENERAL PROCEDURES GOVERNMENT ACCOUNTABILITY OFFICE PERSONNEL APPEALS BOARD... Procedures Discovery § 28.44 Taking of depositions. Depositions may be taken before any person not interested...

  3. 4 CFR 28.44 - Taking of depositions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 4 Accounts 1 2011-01-01 2011-01-01 false Taking of depositions. 28.44 Section 28.44 Accounts GOVERNMENT ACCOUNTABILITY OFFICE GENERAL PROCEDURES GOVERNMENT ACCOUNTABILITY OFFICE PERSONNEL APPEALS BOARD... Procedures Discovery § 28.44 Taking of depositions. Depositions may be taken before any person not interested...

  4. Effect of deposition pressure on the morphology and structural properties of carbon nanotubes synthesized by hot-filament chemical vapor deposition.

    PubMed

    Arendse, C J; Malgas, G F; Scriba, M R; Cummings, F R; Knoesen, D

    2007-10-01

    Hot-filament chemical vapor deposition has developed into an attractive method for the synthesis of various carbon nanostructures, including carbon nanotubes. This is primarily due to its versatility, low cost, repeatability, up-scalability, and ease of production. The resulting nano-material synthesized by this technique is dependent on the deposition conditions which can be easily controlled. In this paper we report on the effect of the deposition pressure on the structural properties and morphology of carbon nanotubes synthesized by hot-filament chemical vapor deposition, using Raman spectroscopy and high-resolution scanning electron microscopy, respectively. A 10 nm-thick Ni layer, deposited on a SiO2/Si substrate, was used as catalyst for carbon nanotube growth. Multi-walled carbon nanotubes with diameters ranging from 20-100 nm were synthesized at 500 degrees C with high structural perfection at deposition pressures between 150 and 200 Torr. Raman spectroscopy measurements confirm that the carbon nanotube deposit is homogeneous across the entire substrate area.

  5. The Increasing Importance of Deposition of Reduced Nitrogen ...

    EPA Pesticide Factsheets

    Rapid development of agricultural activities and fossil fuel combustion in the United States has led to a great increase in reactive nitrogen (Nr) emissions in the second half of the twentieth century. These emissions have been linked to excess nitrogen (N) deposition (i.e. deposition exceeding critical loads) in natural ecosystems through dry and wet deposition pathways. U.S. efforts to reduce nitrogen oxides (NOx) emissions since the 1970s have substantially reduced nitrate deposition, as evidenced by decreasing trends in long-term wet deposition data. These decreases in nitrate deposition along with increases in wet ammonium deposition have altered the balance between oxidized (nitrate) and reduced (ammonium) nitrogen deposition. Across most of the U.S., wet deposition has transitioned from being nitrate dominated in the 1980s to ammonium dominated in recent years. Because ammonia has not been a regulated air pollutant in the U.S., it has historically not been commonly measured. Recent measurement efforts, however, provide a more comprehensive look at ammonia concentrations across several regions of the U.S. These data, along with more routine measurements of gas phase nitric acid and fine particle ammonium and nitrate, permit new insight into the balance of oxidized and reduced nitrogen in the total (wet + dry) U.S. inorganic reactive nitrogen deposition budget. Utilizing two years of N-containing gas and fine particle observations from 37 U.S. monitoring si

  6. Mesoscale Particle-Based Model of Electrophoretic Deposition

    DOE PAGES

    Giera, Brian; Zepeda-Ruiz, Luis A.; Pascall, Andrew J.; ...

    2016-12-20

    In this paper, we present and evaluate a semiempirical particle-based model of electrophoretic deposition using extensive mesoscale simulations. We analyze particle configurations in order to observe how colloids accumulate at the electrode and arrange into deposits. In agreement with existing continuum models, the thickness of the deposit increases linearly in time during deposition. Resulting colloidal deposits exhibit a transition between highly ordered and bulk disordered regions that can give rise to an appreciable density gradient under certain simulated conditions. The overall volume fraction increases and falls within a narrow range as the driving force due to the electric field increasesmore » and repulsive intercolloidal interactions decrease. We postulate ordering and stacking within the initial layer(s) dramatically impacts the microstructure of the deposits. Finally, we find a combination of parameters, i.e., electric field and suspension properties, whose interplay enhances colloidal ordering beyond the commonly known approach of only reducing the driving force.« less

  7. Metal organic chemical vapor deposition of environmental barrier coatings for the inhibition of solid deposit formation from heated jet fuel

    NASA Astrophysics Data System (ADS)

    Mohan, Arun Ram

    Solid deposit formation from jet fuel compromises the fuel handling system of an aviation turbine engine and increases the maintenance downtime of an aircraft. The deposit formation process depends upon the composition of the fuel, the nature of metal surfaces that come in contact with the heated fuel and the operating conditions of the engine. The objective of the study is to investigate the effect of substrate surfaces on the amount and nature of solid deposits in the intermediate regime where both autoxidation and pyrolysis play an important role in deposit formation. A particular focus has been directed to examining the effectiveness of barrier coatings produced by metal organic chemical vapor deposition (MOCVD) on metal surfaces for inhibiting the solid deposit formation from jet fuel degradation. In the first part of the experimental study, a commercial Jet-A sample was stressed in a flow reactor on seven different metal surfaces: AISI316, AISI 321, AISI 304, AISI 347, Inconel 600, Inconel 718, Inconel 750X and FecrAlloy. Examination of deposits by thermal and microscopic analysis shows that the solid deposit formation is influenced by the interaction of organosulfur compounds and autoxidation products with the metal surfaces. The nature of metal sulfides was predicted by Fe-Ni-S ternary phase diagram. Thermal stressing on uncoated surfaces produced coke deposits with varying degree of structural order. They are hydrogen-rich and structurally disordered deposits, spherulitic deposits, small carbon particles with relatively ordered structures and large platelets of ordered carbon structures formed by metal catalysis. In the second part of the study, environmental barrier coatings were deposited on tube surfaces to inhibit solid deposit formation from the heated fuel. A new CVD system was configured by the proper choice of components for mass flow, pressure and temperature control in the reactor. A bubbler was designed to deliver the precursor into the reactor

  8. Annealing dependence of residual stress and optical properties of TiO2 thin film deposited by different deposition methods.

    PubMed

    Chen, Hsi-Chao; Lee, Kuan-Shiang; Lee, Cheng-Chung

    2008-05-01

    Titanium oxide (TiO(2)) thin films were prepared by different deposition methods. The methods were E-gun evaporation with ion-assisted deposition (IAD), radio-frequency (RF) ion-beam sputtering, and direct current (DC) magnetron sputtering. Residual stress was released after annealing the films deposited by RF ion-beam or DC magnetron sputtering but not evaporation, and the extinction coefficient varied significantly. The surface roughness of the evaporated films exceeded that of both sputtered films. At the annealing temperature of 300 degrees C, anatase crystallization occurred in evaporated film but not in the RF ion-beam or DC magnetron-sputtered films. TiO(2) films deposited by sputtering were generally more stable during annealing than those deposited by evaporation.

  9. Role of Mineral Deposits in Global Geochemical Cycles

    NASA Astrophysics Data System (ADS)

    Kesler, S.; Wilkinson, B.

    2009-12-01

    Mineral deposits represent the most extreme degree of natural concentration for most elements and their formation and destruction are important parts of global geochemical cycles. Quantitative estimates of the role that mineral deposits play in these geochemical cycles has been limited, however, by the lack of information on actual amounts of elements that are concentrated in these deposits, and their rates of formation and destruction at geologic time scales. Recent use of a “tectonic diffusion” model for porphyry copper deposits, the most important source of world copper, in conjunction with estimates of their copper content (Kesler and Wilkinson, 2008), allows an assessment of the role of copper deposits in Earth’s global copper cycles. These results indicate that ~4.5*10^8 Gg of Cu have been concentrated in porphyry copper deposits through Phanerozoic time, that deposits containing ~2.8*10^8 Gg of Cu have been removed by uplift and erosion over the same time period, and that deposits containing ~1.7*10^8 Gg remain in Earth’s crust. If styles of formation and destruction of other copper-bearing mineral deposits are similar, then all crustal deposits contain ~3*10^8 Gg of copper. This constitutes about 0.03% of the copper that resides in crustal rocks and provides a first-ever estimate of the rate at which natural geochemical cycles produce the extreme concentrations that constitute mineral deposits. Another ~8*10^8 Gg of copper have been destroyed during the uplift and erosion of mineral deposits over Phanerozoic time, a flux amounting to an annual contribution of about 1.5 Gg of copper to the near-surface environment. This amount is similar in magnitude to copper released by volcanic outgassing, but only ~2.5% of the 56 Gg of copper estimated to be released annually by weathering of average crustal rocks (Rauch and Graedel, 2007). The amount of copper removed from mineral deposits by mining, 1.1*10^4 Gg/year, is much larger than any natural

  10. The Grainsize Characteristics of Coignimbrite Deposits

    NASA Astrophysics Data System (ADS)

    Engwell, Samantha; Eychenne, Julia

    2015-04-01

    Due to their long atmospheric residence time, identifying the source and understanding the dispersion processes of fine-grained ash is of great importance when considering volcanic hazard and risk. An exceptionally efficient mechanism to supply large volumes of fine-grained ash to the stratosphere is the formation of co-ignimbrite plumes. Such plumes form as air is entrained at the top of propagating pyroclastic density currents, allowing a neutrally buoyant package of gas and ash to loft to high altitudes, consequently dispersing over large areas. The study of ash deposits on land and in deep sea cores has demonstrated that such events have played a major role during ignimbrite-forming eruptions, including the Tambora 1815, the Minoan (Santorini), the Campanian Ignimbrite, and the Younger Toba Tuff eruptions, as well as during more recent, pyroclastic flow-forming, intermediate sized eruptions (Vulcanian to Plinian in style), e.g. Mount St. Helens 1980, Fugen-dake (Unzen) 1991, Pinatubo 1991, Montserrat 1997 and Tungurahua 2006 eruptions. Published, as well as new results from the study of co-ignimbrite deposits, show that co-ignimbrite plumes can rise to high altitudes into the atmosphere (the co-ignimbrite plumes from the May 18, 1980 Mount St Helens blast and the Campanian Ignimbrite eruptions reached 30 - 35 km a.s.l,), potentially distribute enormous volumes of ash (the 75 ka Toba eruption and the Minoan eruption of Santorini settled >800 km3 and >25 km3 of co-ignimbrite ash, respectively), and contribute much of the ash to very large (60±6 vol% of the Campanian fallout deposit 130 to 900 km from vent), as well as intermediate size (up to 58 wt% and 52 wt% in the 2006 Tungurahua and May 18, 1980 Mount St. Helens fallout deposits, respectively) explosive eruptions. Comparison of new data with those from the published record shows that co-ignimbrite deposits are strikingly similar, regardless of eruption conditions, and have distinct grain size characteristics

  11. 5 CFR 842.307 - Deposits for military service.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 5 Administrative Personnel 2 2010-01-01 2010-01-01 false Deposits for military service. 842.307... Deposits for military service. (a) Eligibility to make a deposit. (1) An employee or Member subject to FERS may make a deposit for any distinct period of military service by filing an application in a form...

  12. The role of deposits in tsunami risk assessment

    USGS Publications Warehouse

    Jaffe, B.

    2008-01-01

    An incomplete catalogue of tsunamis in the written record hinders tsunami risk assessment. Tsunami deposits, hard evidence of tsunami, can be used to extend the written record. The two primary factors in tsunami risk, tsunami frequency and magnitude, can be addressed through field and modeling studies of tsunami deposits. Recent research has increased the utility of tsunami deposits in tsunami risk assessment by improving the ability to identify tsunami deposits and developing models to determine tsunami magnitude from deposit characteristics. Copyright ASCE 2008.

  13. 76 FR 41392 - Interest on Deposits; Deposit Insurance Coverage

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-14

    ... the statutory prohibition against the payment of interest on demand deposits, effective one year from... continues to read as follows: 12 U.S.C. 1813(l), 1813(m), 1817(i), 1818(q), 1819(Tenth), 1820(f), 1821(a...

  14. Magmatic sulfide-rich nickel-copper deposits related to picrite and (or) tholeiitic basalt dike-sill complexes-A preliminary deposit model

    USGS Publications Warehouse

    Schulz, Klaus J.; Chandler, Val W.; Nicholson, Suzanne W.; Piatak, Nadine M.; Seal, Robert R.; Woodruff, Laurel G.; Zientek, Michael L.

    2010-01-01

    Magmatic sulfide deposits containing nickel (Ni) and copper (Cu), with or without (?) platinum-group elements (PGEs), account for approximately 60 percent of the world's Ni production and are active exploration targets in the United States and elsewhere. On the basis of their principal metal production, magmatic sulfide deposits in mafic rocks can be divided into two major types: those that are sulfide-rich, typically with 10 to 90 percent sulfide minerals, and have economic value primarily because of their Ni and Cu contents; and those that are sulfide-poor, typically with 0.5 to 5 percent sulfide minerals, and are exploited principally for PGE. Because the purpose of this deposit model is to facilitate the assessment for undiscovered, potentially economic magmatic Ni-Cu?PGE sulfide deposits in the United States, it addresses only those deposits of economic significance that are likely to occur in the United States on the basis of known geology. Thus, this model focuses on deposits hosted by small- to medium-sized mafic and (or) ultramafic dikes and sills that are related to picrite and tholeiitic basalt magmatic systems generally emplaced in continental settings as a component of large igneous provinces (LIPs). World-class examples (those containing greater than 1 million tons Ni) of this deposit type include deposits at Noril'sk-Talnakh (Russia), Jinchuan (China), Pechenga (Russia), Voisey's Bay (Canada), and Kabanga (Tanzania). In the United States, this deposit type is represented by the Eagle deposit in northern Michigan, currently under development by Kennecott Minerals.

  15. 8 CFR 1003.35 - Depositions and subpoenas.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 8 Aliens and Nationality 1 2011-01-01 2011-01-01 false Depositions and subpoenas. 1003.35 Section... PROVISIONS EXECUTIVE OFFICE FOR IMMIGRATION REVIEW Immigration Court-Rules of Procedure § 1003.35 Depositions and subpoenas. (a) Depositions. If an Immigration Judge is satisfied that a witness is not reasonably...

  16. 8 CFR 1003.35 - Depositions and subpoenas.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 8 Aliens and Nationality 1 2010-01-01 2010-01-01 false Depositions and subpoenas. 1003.35 Section... PROVISIONS EXECUTIVE OFFICE FOR IMMIGRATION REVIEW Immigration Court-Rules of Procedure § 1003.35 Depositions and subpoenas. (a) Depositions. If an Immigration Judge is satisfied that a witness is not reasonably...

  17. Enzymatic control of biological deposits in papermaking.

    PubMed

    Hatcher, H J

    1984-01-01

    Deposit control in the pulp and paper industry has traditionally been accomplished by the use of toxic biocides. A method has been found whereby biological deposits can be controlled by the use of an enzyme-based product. Numerous field studies have been conducted successfully and photographs prepared illustrating the process. The dynamics of deposit formation and problems associated with such formations have been the subject of considerable study. Development and control of deposit problems under different paper mill conditions using the chemical-biochemical approach will be discussed.

  18. A preliminary deposit model for lithium brines

    USGS Publications Warehouse

    Bradley, Dwight; Munk, LeeAnn; Jochens, Hillary; Hynek, Scott; Labay, Keith A.

    2013-01-01

    This report is part of an effort by the U.S. Geological Survey to update existing mineral deposit models and to develop new ones. The global transition away from hydrocarbons toward energy alternatives increases demand for many scarce metals. Among these is lithium, a key component of lithium-ion batteries for electric and hybrid vehicles. Lithium brine deposits account for about three-fourths of the world’s lithium production. Updating an earlier deposit model, we emphasize geologic information that might directly or indirectly help in exploration for lithium brine deposits, or for assessing regions for mineral resource potential. Special attention is given to the best-known deposit in the world—Clayton Valley, Nevada, and to the giant Salar de Atacama, Chile.

  19. Tellurium, a guide to mineral deposits

    USGS Publications Warehouse

    Watterson, J.R.; Gott, G.B.; Neuerburg, G.J.; Lakin, H.W.; Cathrall, J.B.

    1977-01-01

    Te dispersion patterns are useful in exploring for different types of mineral deposits and in providing additional information about known ore deposits. The Te content of rocks is given for five mining districts in the western United States: Coeur d'Alene, Idaho; Robinson, near Ely, Nevada; Montezuma, Colorado; Crater Creek area, Colorado; Cripple Creek, Colorado. Many of the analyses were obtained by use of a new analytical method sensitive to 0.001 ppm Te. The principal ore deposits in the Coeur d'Alene district, Idaho, are Pb-Zn-Ag replacement veins in Precambrian rocks of the Belt Supergroup. Te dispersion patterns show the outlines of the original mineral belts, the effects of intrusive events, the location of ore deposits, the displacements caused by post-ore faulting, and the borders of the 780-km2 district. The disseminated porphyry Cu deposits of the Robinson mining district, Nevada, are associated with Cretaceous quartz monzonite stocks that have intruded Palaeozoic carbonate rocks. Te is present in rock samples in concentrations as high as 10,000 ppm and forms a halo around the areas containing the Cu deposits. The alteration zones in the porphyry Mo district near Montezuma, Colorado, are developed around several small Tertiary intrusions occurring along a regional shear zone. Te haloes reflect the locations of porphyry intrusives, individual deposits and their ore shoots, and the pattern and intensity of adjacent alteration. The Te content of soils over the Montezuma stock is higher than, and varies independently from, the Te content of adjacent outcrops. Soils generally contain more Te than adjacent outcropping rocks. Soil may collect gaseous Te compounds from mineral deposits. The Crater Creek area is a northwestern extension of the Summitville mining district, Colorado. Te dispersion patterns radiate out from exposed Cu-Pb-Zn veins, from an outcrop of molybdenite stockwork veins and from associated iron-stained altered rock. Te haloes intensify

  20. Characterizing avulsion stratigraphy in ancient alluvial deposits

    NASA Astrophysics Data System (ADS)

    Jones, H. L.; Hajek, E. A.

    2007-11-01

    Guidelines for identifying ancient avulsion deposits were set forth by Kraus and Wells [Kraus, M.J., Wells, T.M., 1999. Recognizing avulsion deposits in the ancient stratigraphical record. In: Smith, N.D., Rogers, J. (Eds.), Fluvial Sedimentology VI, Special Publication of the International Association of Sedimentologists, vol. 28, pp. 251-268], building on the study by Smith et al. [Smith, N.D., Cross, T.A., Dufficy, J.P., Clough, S.R., 1989. Anatomy of an avulsion. Sedimentology 36, 1-23] of the modern Saskatchewan River system (Cumberland Marshes, central Canada), and serve to characterize avulsion depositional sequences in the ancient Willwood and Fort Union Formations (Paleogene, Bighorn Basin, NW Wyoming, USA). We recognize, however, that the model is not universally applicable to avulsion-dominated successions, specifically systems which lack defining "heterolithic avulsion deposits", set forth by Kraus and Wells [Kraus, M.J., Wells, T.M., 1999. Recognizing avulsion deposits in the ancient stratigraphical record. In: Smith, N.D., Rogers, J. (Eds.), Fluvial Sedimentology VI, Special Publication of the International Association of Sedimentologists, vol. 28, pp. 251-268]. Observations in several fluvial intervals suggest that the avulsion stratigraphy outlined by Kraus and Wells [Kraus, M.J., Wells, T.M., 1999. Recognizing avulsion deposits in the ancient stratigraphical record. In: Smith, N.D., Rogers, J. (Eds.), Fluvial Sedimentology VI, Special Publication of the International Association of Sedimentologists, vol. 28, pp. 251-268] represents one category of avulsion stratigraphy found in the rock record, but does not capture the nature of avulsion deposits everywhere. Based on observations (using measured sections, outcrop photo-panels, and aerial photographs) in the Willwood Formation (Eocene, Wyoming) and Ferris Formation (Cretaceous/Paleogene, Wyoming), we present two end-member categories of avulsion stratigraphy in ancient deposits; stratigraphically

  1. 12 CFR 217.3 - Interest on demand deposits.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... on a time deposit for not more than ten calendar days; (1) Where the member bank has provided in the time deposit contract that, if the deposit or any portion thereof is withdrawn not more than ten... maturity date and the date of renewal of the deposit, provided that such certificate is renewed within ten...

  2. 47 CFR 1.318 - The taking of depositions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 47 Telecommunication 1 2011-10-01 2011-10-01 false The taking of depositions. 1.318 Section 1.318... and Preservation of Evidence § 1.318 The taking of depositions. (a) Persons before whom depositions may be taken. Depositions shall be taken before any judge of any court of the United States; any U.S...

  3. 47 CFR 1.318 - The taking of depositions.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 47 Telecommunication 1 2010-10-01 2010-10-01 false The taking of depositions. 1.318 Section 1.318... and Preservation of Evidence § 1.318 The taking of depositions. (a) Persons before whom depositions may be taken. Depositions shall be taken before any judge of any court of the United States; any U.S...

  4. The talc, soapstone, and asbestos deposits of Massachusetts

    USGS Publications Warehouse

    Chute, Newton Earl

    1969-01-01

    Several talc and soapstone deposits were worked in Massachusetts from about 1810 to 1922. Most of these deposits are in the Chester Amphibolite, or in serpentine lenses in or adjacent to the amphibolite along a belt that extends north-south across the State from Rowe to West Granville; it appears to be a continuation of the Vermont talc belt. The only deposits outside of this belt that have been worked are a talc and soapstone deposit in the north-west corner of Hinsdale and soapstone deposits on the east side of Soapstone Hill in the western part of Petersham. Very little asbestos has been produced in Massachusetts. A small amount of anthophyllite asbestos was obtained from the deposit in Hinsdale, and from a deposit in southwestern Pelham. The talc and soapstone deposits of Massachusetts were formed from serpentine and possibly from amphibolite, schist, and dolomitic limestone. Those fromed from serpentine are mainly at the ends of the serpentine bodies, and those that appear to have been formed from amphibolite or schist are on the faults and folds.

  5. CMAS Interactions with Advanced Environmental Barrier Coatings Deposited via Plasma Spray- Physical Vapor Deposition

    NASA Technical Reports Server (NTRS)

    Harder, B. J.; Wiesner, V. L.; Zhu, D.; Johnson, N. S.

    2017-01-01

    Materials for advanced turbine engines are expected to have temperature capabilities in the range of 1370-1500C. At these temperatures the ingestion of sand and dust particulate can result in the formation of corrosive glass deposits referred to as CMAS. The presence of this glass can both thermomechanically and thermochemically significantly degrade protective coatings on metallic and ceramic components. Plasma Spray- Physical Vapor Deposition (PS-PVD) was used to deposit advanced environmental barrier coating (EBC) systems for investigation on their interaction with CMAS compositions. Coatings were exposed to CMAS and furnace tested in air from 1 to 50 hours at temperatures ranging from 1200-1500C. Coating composition and crystal structure were tracked with X-ray diffraction and microstructure with electron microscopy.

  6. Surface Finish after Laser Metal Deposition

    NASA Astrophysics Data System (ADS)

    Rombouts, M.; Maes, G.; Hendrix, W.; Delarbre, E.; Motmans, F.

    Laser metal deposition (LMD) is an additive manufacturing technology for the fabrication of metal parts through layerwise deposition and laser induced melting of metal powder. The poor surface finish presents a major limitation in LMD. This study focuses on the effects of surface inclination angle and strategies to improve the surface finish of LMD components. A substantial improvement in surface quality of both the side and top surfaces has been obtained by laser remelting after powder deposition.

  7. 76 FR 21265 - Interest on Deposits; Deposit Insurance Coverage

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-15

    ... of interest on demand deposits, effective one year from the date of the DFA's enactment, July 21... COVERAGE 2. The authority for part 330 continues to read as follows: 12 U.S.C. 1813(l), 1813(m), 1817(i...

  8. 10 CFR 2.1019 - Depositions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... Applicable to Proceedings for the Issuance of Licenses for the Receipt of High-Level Radioactive Waste at a... the failure to sign, and shall promptly transmit an electronic copy of the deposition to the Secretary of the Commission for entry into the electronic docket. (e) Where the deposition is to be taken on...

  9. 10 CFR 2.1019 - Depositions.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... Issuance of Licenses for the Receipt of High-Level Radioactive Waste at a Geologic Repository § 2.1019... the failure to sign, and shall promptly transmit an electronic copy of the deposition to the Secretary of the Commission for entry into the electronic docket. (e) Where the deposition is to be taken on...

  10. 10 CFR 2.1019 - Depositions.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... Issuance of Licenses for the Receipt of High-Level Radioactive Waste at a Geologic Repository § 2.1019... the failure to sign, and shall promptly transmit an electronic copy of the deposition to the Secretary of the Commission for entry into the electronic docket. (e) Where the deposition is to be taken on...

  11. Geology of the manganese deposits of Cuba

    USGS Publications Warehouse

    Simons, Frank S.; Straczek, John A.

    1958-01-01

    Deposits of manganese ore have been found in five of the six provinces of Cuba and have been reported from the sixth.  Only Oriente and Pinar del Rio provinces have more than a few known deposits and only the deposits of Oriente have yielded any appreciable amount of ore.

  12. 46 CFR 287.20 - Obligation of deposits.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 8 2010-10-01 2010-10-01 false Obligation of deposits. 287.20 Section 287.20 Shipping... OPERATORS ESTABLISHMENT OF CONSTRUCTION RESERVE FUNDS § 287.20 Obligation of deposits. (a) Time for obligation. Within three years from the date of any deposit in a construction reserve fund, unless extension...

  13. Atmospheric deposition maps for the Rocky Mountains

    USGS Publications Warehouse

    Nanus, L.; Campbell, D.H.; Ingersoll, G.P.; Clow, D.W.; Mast, M.A.

    2003-01-01

    Variability in atmospheric deposition across the Rocky Mountains is influenced by elevation, slope, aspect, and precipitation amount and by regional and local sources of air pollution. To improve estimates of deposition in mountainous regions, maps of average annual atmospheric deposition loadings of nitrate, sulfate, and acidity were developed for the Rocky Mountains by using spatial statistics. A parameter-elevation regressions on independent slopes model (PRISM) was incorporated to account for variations in precipitation amount over mountainous regions. Chemical data were obtained from the National Atmospheric Deposition Program/National Trends Network and from annual snowpack surveys conducted by the US Geological Survey and National Park Service, in cooperation with other Federal, State and local agencies. Surface concentration maps were created by ordinary kriging in a geographic information system, using a local trend and mathematical model to estimate the spatial variance. Atmospheric-deposition maps were constructed at 1-km resolution by multiplying surface concentrations from the kriged grid and estimates of precipitation amount from the PRISM model. Maps indicate an increasing spatial trend in concentration and deposition of the modeled constituents, particularly nitrate and sulfate, from north to south throughout the Rocky Mountains and identify hot-spots of atmospheric deposition that result from combined local and regional sources of air pollution. Highest nitrate (2.5-3.0kg/ha N) and sulfate (10.0-12.0kg/ha SO4) deposition is found in northern Colorado.

  14. Sputter deposition for multi-component thin films

    DOEpatents

    Krauss, A.R.; Auciello, O.

    1990-05-08

    Ion beam sputter-induced deposition using a single ion beam and a multicomponent target is capable of reproducibly producing thin films of arbitrary composition, including those which are close to stoichiometry. Using a quartz crystal deposition monitor and a computer controlled, well-focused ion beam, this sputter-deposition approach is capable of producing metal oxide superconductors and semiconductors of the superlattice type such as GaAs-AlGaAs as well as layered metal/oxide/semiconductor/superconductor structures. By programming the dwell time for each target according to the known sputtering yield and desired layer thickness for each material, it is possible to deposit composite films from a well-controlled sub-monolayer up to thicknesses determined only by the available deposition time. In one embodiment, an ion beam is sequentially directed via a set of X-Y electrostatic deflection plates onto three or more different element or compound targets which are constituents of the desired film. In another embodiment, the ion beam is directed through an aperture in the deposition plate and is displaced under computer control to provide a high degree of control over the deposited layer. In yet another embodiment, a single fixed ion beam is directed onto a plurality of sputter targets in a sequential manner where the targets are each moved in alignment with the beam under computer control in forming a multilayer thin film. This controlled sputter-deposition approach may also be used with laser and electron beams. 10 figs.

  15. Sputter deposition for multi-component thin films

    DOEpatents

    Krauss, Alan R.; Auciello, Orlando

    1990-01-01

    Ion beam sputter-induced deposition using a single ion beam and a multicomponent target is capable of reproducibly producing thin films of arbitrary composition, including those which are close to stoichiometry. Using a quartz crystal deposition monitor and a computer controlled, well-focused ion beam, this sputter-deposition approach is capable of producing metal oxide superconductors and semiconductors of the superlattice type such as GaAs-AlGaAs as well as layered metal/oxide/semiconductor/superconductor structures. By programming the dwell time for each target according to the known sputtering yield and desired layer thickness for each material, it is possible to deposit composite films from a well-controlled sub-monolayer up to thicknesses determined only by the available deposition time. In one embodiment, an ion beam is sequentially directed via a set of X-Y electrostatic deflection plates onto three or more different element or compound targets which are constituents of the desired film. In another embodiment, the ion beam is directed through an aperture in the deposition plate and is displaced under computer control to provide a high degree of control over the deposited layer. In yet another embodiment, a single fixed ion beam is directed onto a plurality of sputter targets in a sequential manner where the targets are each moved in alignment with the beam under computer control in forming a multilayer thin film. This controlled sputter-deposition approach may also be used with laser and electron beams.

  16. Fog deposition to the Atacama desert

    NASA Astrophysics Data System (ADS)

    Westbeld, A.; Klemm, O.; Griessbaum, F.; Sträter, E.; Larrain, H.; Osses, P.; Cereceda, P.

    2010-07-01

    In the Atacama Desert, one of the driest places on earth, fog deposition plays an important role for the water balance and for the survival of vulnerable ecosystems. The eddy covariance method, previously applied for the quantification of fog deposition to forests in various parts of the world, was used for the first time to measure deposition of fog water to a desert. We estimated the amount of water available for the ecosystem by deposition and determined the relevant processes driving fog deposition. This is especially important for the species Tillandsia landbecki living in coastal Atacama at the limit of plant existence with fog and dew being the only sources of liquid water. Between 31 July and 19 August, 2008, measurements were realized in a 31 ha large Tillandsia carpet at Cerro Guanaco, located 15 km south of Iquique, northern Chile. Several data quality assurance procedures were applied. For the values in compliance with the applied criteria, the mean total deposition per hour was determined (0.04 L per m2) for foggy periods. This number was applied to estimate the amount of water deposited during the measuring period, during the entire month of August 2008, and throughout a whole year. For August 2008, a frequency of fog of 16 %, as established during the measuring period, was assumed. The frequency for a whole year was estimated from the differences of the collected amount of water obtained with standard fog collectors installed at Cerro Guanaco in an earlier study. Calculations resulted in an amount of 2.5 L per m2 of deposited fog water for the measuring period. During the entire August, 4.4 L per m2 have likely been available, and for a whole year, a total of 25 L per m2 was estimated to have reached the surface. Inaccuracies could have been caused by the low amount of data applied, and by a possible underestimation of the deposition due to additional formation of radiation fog during the fog events. Three days were used for further analysis because

  17. Deposition of adherent Ag-Ti duplex films on ceramics in a multiple-cathode sputter deposition system

    NASA Technical Reports Server (NTRS)

    Honecy, Frank S.

    1992-01-01

    The adhesion of Ag films deposited on oxide ceramics can be increased by first depositing intermediate films of active metals such as Ti. Such duplex coatings can be fabricated in a widely used three target sputter deposition system. It is shown here that the beneficial effect of the intermediate Ti film can be defeated by commonly used in situ target and substrate sputter cleaning procedures which result in Ag under the Ti. Auger electron spectroscopy and wear testing of the coatings are used to develop a cleaning strategy resulting in an adherent film system.

  18. Physical Vapor Deposition of Thin Films

    NASA Astrophysics Data System (ADS)

    Mahan, John E.

    2000-01-01

    A unified treatment of the theories, data, and technologies underlying physical vapor deposition methods With electronic, optical, and magnetic coating technologies increasingly dominating manufacturing in the high-tech industries, there is a growing need for expertise in physical vapor deposition of thin films. This important new work provides researchers and engineers in this field with the information they need to tackle thin film processes in the real world. Presenting a cohesive, thoroughly developed treatment of both fundamental and applied topics, Physical Vapor Deposition of Thin Films incorporates many critical results from across the literature as it imparts a working knowledge of a variety of present-day techniques. Numerous worked examples, extensive references, and more than 100 illustrations and photographs accompany coverage of: * Thermal evaporation, sputtering, and pulsed laser deposition techniques * Key theories and phenomena, including the kinetic theory of gases, adsorption and condensation, high-vacuum pumping dynamics, and sputtering discharges * Trends in sputter yield data and a new simplified collisional model of sputter yield for pure element targets * Quantitative models for film deposition rate, thickness profiles, and thermalization of the sputtered beam

  19. Vacuum-deposited polymer/silver reflector material

    NASA Astrophysics Data System (ADS)

    Affinito, John D.; Martin, Peter M.; Gross, Mark E.; Bennett, Wendy D.

    1994-09-01

    Weatherable, low cost, front surface, solar reflectors on flexible substrates would be highly desirable for lamination to solar concentrator panels. The method to be described in this paper may permit such reflector material to be fabricated for less the 50$CNT per square foot. Vacuum deposited Polymer/Silver/Polymer reflectors and Fabry-Perot interference filters were fabricated in a vacuum web coating operation on polyester substrates. Reflectivities were measured in the wavelength range from .4 micrometers to .8 micrometers . It is hoped that a low cost substrate can be used with the substrate laminated to the concentrator and the weatherable acrylic polymer coating facing the sun. This technique should be capable of deposition line speeds approaching 1500 linear feet/minute2. Central to this technique is a new vacuum deposition process for the high rate deposition of polymer films. This polymer process involves the flash evaporation of an acrylic monomer onto a moving substrate. The monomer is subsequently cured by an electron beam or ultraviolet light. This high speed polymer film deposition process has been named the PML process- for Polymer Multi- Layer.

  20. Method for deposition of a conductor in integrated circuits

    DOEpatents

    Creighton, J.R.; Dominguez, F.; Johnson, A.W.; Omstead, T.R.

    1997-09-02

    A method is described for fabricating integrated semiconductor circuits and, more particularly, for the selective deposition of a conductor onto a substrate employing a chemical vapor deposition process. By way of example, tungsten can be selectively deposited onto a silicon substrate. At the onset of loss of selectivity of deposition of tungsten onto the silicon substrate, the deposition process is interrupted and unwanted tungsten which has deposited on a mask layer with the silicon substrate can be removed employing a halogen etchant. Thereafter, a plurality of deposition/etch back cycles can be carried out to achieve a predetermined thickness of tungsten. 2 figs.

  1. Method for deposition of a conductor in integrated circuits

    DOEpatents

    Creighton, J. Randall; Dominguez, Frank; Johnson, A. Wayne; Omstead, Thomas R.

    1997-01-01

    A method is described for fabricating integrated semiconductor circuits and, more particularly, for the selective deposition of a conductor onto a substrate employing a chemical vapor deposition process. By way of example, tungsten can be selectively deposited onto a silicon substrate. At the onset of loss of selectivity of deposition of tungsten onto the silicon substrate, the deposition process is interrupted and unwanted tungsten which has deposited on a mask layer with the silicon substrate can be removed employing a halogen etchant. Thereafter, a plurality of deposition/etch back cycles can be carried out to achieve a predetermined thickness of tungsten.

  2. 31 CFR 344.4 - What are Time Deposit securities?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... LOCAL GOVERNMENT SERIES Time Deposit Securities § 344.4 What are Time Deposit securities? Time Deposit... 31 Money and Finance: Treasury 2 2010-07-01 2010-07-01 false What are Time Deposit securities? 344...? The issuer must fix the maturity periods for Time Deposit securities, which are issued as follows: (1...

  3. 31 CFR 344.4 - What are Time Deposit securities?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... LOCAL GOVERNMENT SERIES Time Deposit Securities § 344.4 What are Time Deposit securities? Time Deposit... 31 Money and Finance:Treasury 2 2011-07-01 2011-07-01 false What are Time Deposit securities? 344...? The issuer must fix the maturity periods for Time Deposit securities, which are issued as follows: (1...

  4. 31 CFR 344.4 - What are Time Deposit securities?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... LOCAL GOVERNMENT SERIES Time Deposit Securities § 344.4 What are Time Deposit securities? Time Deposit... 31 Money and Finance:Treasury 2 2013-07-01 2013-07-01 false What are Time Deposit securities? 344...? The issuer must fix the maturity periods for Time Deposit securities, which are issued as follows: (1...

  5. 31 CFR 344.4 - What are Time Deposit securities?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... LOCAL GOVERNMENT SERIES Time Deposit Securities § 344.4 What are Time Deposit securities? Time Deposit... 31 Money and Finance:Treasury 2 2012-07-01 2012-07-01 false What are Time Deposit securities? 344...? The issuer must fix the maturity periods for Time Deposit securities, which are issued as follows: (1...

  6. Method of depositing a high-emissivity layer

    DOEpatents

    Wickersham, Charles E.; Foster, Ellis L.

    1983-01-01

    A method of depositing a high-emissivity layer on a substrate comprising RF sputter deposition of a carbide-containing target in an atmosphere of a hydrocarbon gas and a noble gas. As the carbide is deposited on the substrate the hydrocarbon gas decomposes to hydrogen and carbon. The carbon deposits on the target and substrate causing a carbide/carbon composition gradient to form on the substrate. At a sufficiently high partial pressure of hydrocarbon gas, a film of high-emissivity pure carbon will eventually form over the substrate.

  7. The modelling routes for the chemical vapour deposition process: application to Si 1- xGe x deposition

    NASA Astrophysics Data System (ADS)

    Pons, M.; Bernard, C.; Rouch, H.; Madar, R.

    1995-10-01

    The purpose of this article is to present the modelling routes for the chemical vapour deposition process with a special emphasis on mass transport models with near local thermochemical equilibrium imposed in the gas-phase and at the deposition surface. The theoretical problems arising from the linking of the two selected approaches, thermodynamics and mass transport, are shown and a solution procedure is proposed. As an illustration, selected results of thermodynamic and mass transport analysis and of the coupled approach showed that, for the deposition of Si 1- xGe x solid solution at 1300 K (system SiGeClHAr), the thermodynamic heterogeneous stability of the reactive gases and the thermal diffusion led to the germanium depletion of the deposit.

  8. 24 CFR 291.535 - Earnest money deposit.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 24 Housing and Urban Development 2 2012-04-01 2012-04-01 false Earnest money deposit. 291.535... Next Door Sales Program § 291.535 Earnest money deposit. (a) General. The earnest money deposit is the sum of money that must be paid by the law enforcement officer, teacher, or firefighter/emergency...

  9. 24 CFR 291.535 - Earnest money deposit.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 24 Housing and Urban Development 2 2014-04-01 2014-04-01 false Earnest money deposit. 291.535... Next Door Sales Program § 291.535 Earnest money deposit. (a) General. The earnest money deposit is the sum of money that must be paid by the law enforcement officer, teacher, or firefighter/emergency...

  10. 24 CFR 291.535 - Earnest money deposit.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 24 Housing and Urban Development 2 2011-04-01 2011-04-01 false Earnest money deposit. 291.535... Next Door Sales Program § 291.535 Earnest money deposit. (a) General. The earnest money deposit is the sum of money that must be paid by the law enforcement officer, teacher, or firefighter/emergency...

  11. 24 CFR 291.535 - Earnest money deposit.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 24 Housing and Urban Development 2 2013-04-01 2013-04-01 false Earnest money deposit. 291.535... Next Door Sales Program § 291.535 Earnest money deposit. (a) General. The earnest money deposit is the sum of money that must be paid by the law enforcement officer, teacher, or firefighter/emergency...

  12. 24 CFR 291.535 - Earnest money deposit.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 24 Housing and Urban Development 2 2010-04-01 2010-04-01 false Earnest money deposit. 291.535... Next Door Sales Program § 291.535 Earnest money deposit. (a) General. The earnest money deposit is the sum of money that must be paid by the law enforcement officer, teacher, or firefighter/emergency...

  13. 45 CFR 501.5 - Depositions.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... is expected the witness will testify, and the time and place proposed for the taking of the... served upon all parties at least 10 days prior to the date of the taking of the deposition. (b) Who may... the time and place specified in the Commission's order, the officer taking the deposition will permit...

  14. 45 CFR 501.5 - Depositions.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... is expected the witness will testify, and the time and place proposed for the taking of the... served upon all parties at least 10 days prior to the date of the taking of the deposition. (b) Who may... the time and place specified in the Commission's order, the officer taking the deposition will permit...

  15. 45 CFR 501.5 - Depositions.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... is expected the witness will testify, and the time and place proposed for the taking of the... served upon all parties at least 10 days prior to the date of the taking of the deposition. (b) Who may... the time and place specified in the Commission's order, the officer taking the deposition will permit...

  16. 22 CFR 92.52 - “Deposition on notice” defined.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 22 Foreign Relations 1 2011-04-01 2011-04-01 false âDeposition on noticeâ defined. 92.52 Section... Depositions and Letters Rogatory § 92.52 “Deposition on notice” defined. A deposition on notice is a deposition taken before a competent official after reasonable notice has been given in writing by the party...

  17. 22 CFR 92.52 - “Deposition on notice” defined.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 22 Foreign Relations 1 2010-04-01 2010-04-01 false âDeposition on noticeâ defined. 92.52 Section... Depositions and Letters Rogatory § 92.52 “Deposition on notice” defined. A deposition on notice is a deposition taken before a competent official after reasonable notice has been given in writing by the party...

  18. Sputter-deposited fuel cell membranes and electrodes

    NASA Technical Reports Server (NTRS)

    Narayanan, Sekharipuram R. (Inventor); Jeffries-Nakamura, Barbara (Inventor); Chun, William (Inventor); Ruiz, Ron P. (Inventor); Valdez, Thomas I. (Inventor)

    2001-01-01

    A method for preparing a membrane for use in a fuel cell membrane electrode assembly includes the steps of providing an electrolyte membrane, and sputter-depositing a catalyst onto the electrolyte membrane. The sputter-deposited catalyst may be applied to multiple sides of the electrolyte membrane. A method for forming an electrode for use in a fuel cell membrane electrode assembly includes the steps of obtaining a catalyst, obtaining a backing, and sputter-depositing the catalyst onto the backing. The membranes and electrodes are useful for assembling fuel cells that include an anode electrode, a cathode electrode, a fuel supply, and an electrolyte membrane, wherein the electrolyte membrane includes a sputter-deposited catalyst, and the sputter-deposited catalyst is effective for sustaining a voltage across a membrane electrode assembly in the fuel cell.

  19. A lithium deposition system for tokamak devices*

    NASA Astrophysics Data System (ADS)

    Graziul, Christopher; Majeski, Richard; Kaita, Robert; Hoffman, Daniel; Timberlake, John; Card, David

    2002-11-01

    The production of a lithium deposition system using commercially available components is discussed. This system is intended to provide a fresh lithium wall coating between discharges in a tokamak. For this purpose, a film 100-200 Å thick is sufficient to ensure that the plasma interacts solely with the lithium. A test system consisting of a lithium evaporator and a deposition monitor has been designed and constructed to investigate deposition rates and coverage. A Thermionics 3kW e-gun is used to rapidly evaporate small amounts of solid lithium. An Inficon XTM/2 quartz deposition monitor then measures deposition rate at varying distances, positions and angles relative to the e-gun crucible. Initial results from the test system will be presented. *Supported by US DOE contract #DE-AC02-76CH-03073

  20. Combustion system processes leading to corrosive deposits

    NASA Technical Reports Server (NTRS)

    Stearns, C. A.; Kohl, F. J.; Rosner, D. E.

    1981-01-01

    Degradation of turbine engine hot gas path components by high temperature corrosion can usually be associated with deposits even though other factors may also play a significant role. The origins of the corrosive deposits are traceable to chemical reactions which take place during the combustion process. In the case of hot corrosion/sulfidation, sodium sulfate was established as the deposited corrosive agent even when none of this salt enters the engine directly. The sodium sulfate is formed during the combustion and deposition processes from compounds of sulfur contained in the fuel as low level impurities and sodium compounds, such as sodium chloride, ingested with intake air. In other turbine and power generation situations, corrosive and/or fouling deposits can result from such metals as potassium, iron, calcium, vanadium, magnesium, and silicon.

  1. Electron beam induced deposition of silacyclohexane and dichlorosilacyclohexane: the role of dissociative ionization and dissociative electron attachment in the deposition process.

    PubMed

    P, Ragesh Kumar T; Hari, Sangeetha; Damodaran, Krishna K; Ingólfsson, Oddur; Hagen, Cornelis W

    2017-01-01

    We present first experiments on electron beam induced deposition of silacyclohexane (SCH) and dichlorosilacyclohexane (DCSCH) under a focused high-energy electron beam (FEBID). We compare the deposition dynamics observed when growing pillars of high aspect ratio from these compounds and we compare the proximity effect observed for these compounds. The two precursors show similar behaviour with regards to fragmentation through dissociative ionization in the gas phase under single-collision conditions. However, while DCSCH shows appreciable cross sections with regards to dissociative electron attachment, SCH is inert with respect to this process. We discuss our deposition experiments in context of the efficiency of these different electron-induced fragmentation processes. With regards to the deposition dynamics, we observe a substantially faster growth from DCSCH and a higher saturation diameter when growing pillars with high aspect ratio. However, both compounds show similar behaviour with regards to the proximity effect. With regards to the composition of the deposits, we observe that the C/Si ratio is similar for both compounds and in both cases close to the initial molecular stoichiometry. The oxygen content in the DCSCH deposits is about double that of the SCH deposits. Only marginal chlorine is observed in the deposits of from DCSCH. We discuss these observations in context of potential approaches for Si deposition.

  2. Nanostructure templating using low temperature atomic layer deposition

    DOEpatents

    Grubbs, Robert K [Albuquerque, NM; Bogart, Gregory R [Corrales, NM; Rogers, John A [Champaign, IL

    2011-12-20

    Methods are described for making nanostructures that are mechanically, chemically and thermally stable at desired elevated temperatures, from nanostructure templates having a stability temperature that is less than the desired elevated temperature. The methods comprise depositing by atomic layer deposition (ALD) structural layers that are stable at the desired elevated temperatures, onto a template employing a graded temperature deposition scheme. At least one structural layer is deposited at an initial temperature that is less than or equal to the stability temperature of the template, and subsequent depositions made at incrementally increased deposition temperatures until the desired elevated temperature stability is achieved. Nanostructure templates include three dimensional (3D) polymeric templates having features on the order of 100 nm fabricated by proximity field nanopatterning (PnP) methods.

  3. Nitrogen deposition in California forests: a review

    Treesearch

    Andrzej Bytnerowicz; Mark E. Fenn

    1996-01-01

    Atmospheric concentrations and deposition of the major nitrogenous (N) compounds and their biological effects in California forests are reviewed. Climatic characteristics of California are summarized in light of their effects on pollutant accumulation and transport. Over large areas of the state dry deposition is of greater magnitude than wet deposition due to the arid...

  4. An Introduction to Atomic Layer Deposition

    NASA Technical Reports Server (NTRS)

    Dwivedi, Vivek H.

    2017-01-01

    Atomic Layer Deposition has been instrumental in providing a deposition method for multiple space flight applications. It is well known that ALD is a cost effective nanoadditive-manufacturing technique that allows for the conformal coating of substrates with atomic control in a benign temperature and pressure environment. Through the introduction of paired precursor gases, thin films can be deposited on a myriad of substrates from flat surfaces to those with significant topography. By providing atomic layer control, where single layers of atoms can be deposited, the fabrication of metal transparent films, precise nano-laminates, and coatings of nano-channels, pores and particles is achievable. The feasibility of this technology for NASA line of business applications range from thermal systems, optics, sensors, to environmental protection. An overview of this technology will be presented.

  5. Perspective: Highly stable vapor-deposited glasses

    NASA Astrophysics Data System (ADS)

    Ediger, M. D.

    2017-12-01

    This article describes recent progress in understanding highly stable glasses prepared by physical vapor deposition and provides perspective on further research directions for the field. For a given molecule, vapor-deposited glasses can have higher density and lower enthalpy than any glass that can be prepared by the more traditional route of cooling a liquid, and such glasses also exhibit greatly enhanced kinetic stability. Because vapor-deposited glasses can approach the bottom of the amorphous part of the potential energy landscape, they provide insights into the properties expected for the "ideal glass." Connections between vapor-deposited glasses, liquid-cooled glasses, and deeply supercooled liquids are explored. The generality of stable glass formation for organic molecules is discussed along with the prospects for stable glasses of other types of materials.

  6. Perspective: Highly stable vapor-deposited glasses

    DOE PAGES

    Ediger, M. D.

    2017-12-07

    This paper describes recent progress in understanding highly stable glasses prepared by physical vapor deposition and provides perspective on further research directions for the field. For a given molecule, vapor-deposited glasses can have higher density and lower enthalpy than any glass that can be prepared by the more traditional route of cooling a liquid, and such glasses also exhibit greatly enhanced kinetic stability. Because vapor-deposited glasses can approach the bottom of the amorphous part of the potential energy landscape, they provide insights into the properties expected for the “ideal glass”. Connections between vapor-deposited glasses, liquid-cooled glasses, and deeply supercooled liquidsmore » are explored. The generality of stable glass formation for organic molecules is discussed along with the prospects for stable glasses of other types of materials.« less

  7. Perspective: Highly stable vapor-deposited glasses

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

    Ediger, M. D.

    This paper describes recent progress in understanding highly stable glasses prepared by physical vapor deposition and provides perspective on further research directions for the field. For a given molecule, vapor-deposited glasses can have higher density and lower enthalpy than any glass that can be prepared by the more traditional route of cooling a liquid, and such glasses also exhibit greatly enhanced kinetic stability. Because vapor-deposited glasses can approach the bottom of the amorphous part of the potential energy landscape, they provide insights into the properties expected for the “ideal glass”. Connections between vapor-deposited glasses, liquid-cooled glasses, and deeply supercooled liquidsmore » are explored. The generality of stable glass formation for organic molecules is discussed along with the prospects for stable glasses of other types of materials.« less

  8. 14 CFR 16.215 - Depositions.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... testimony of the witness; or (3) The taking of the deposition is necessary to prevent undue and excessive... application shall include: (1) The name and residence of the witness; (2) The time and place for the taking of... found, or refuses to sign. The reporter shall note the reason for failure to sign. (e) Depositions of...

  9. Electrical and optical performance of transparent conducting oxide films deposited by electrostatic spray assisted vapour deposition.

    PubMed

    Hou, Xianghui; Choy, Kwang-Leong; Liu, Jun-Peng

    2011-09-01

    Transparent conducting oxide (TCO) films have the remarkable combination of high electrical conductivity and optical transparency. There is always a strong motivation to produce TCO films with good performance at low cost. Electrostatic Spray Assisted Vapor Deposition (ESAVD), as a variant of chemical vapour deposition (CVD), is a non-vacuum and low-cost deposition method. Several types of TCO films have been deposited using ESAVD process, including indium tin oxide (ITO), antimony-doped tin oxide (ATO), and fluorine doped tin oxide (FTO). This paper reports the electrical and optical properties of TCO films produced by ESAVD methods, as well as the effects of post treatment by plasma hydrogenation on these TCO films. The possible mechanisms involved during plasma hydrogenation of TCO films are also discussed. Reduction and etching effect during plasma hydrogenation are the most important factors which determine the optical and electrical performance of TCO films.

  10. Modeling of aircraft deicing fluids deposition

    DOT National Transportation Integrated Search

    2000-06-18

    Glycol deposition near aircraft during deicing operations has become an important consideration at major airports. A sampling process was used to quantify glycol deposition from deicing operations at a major international airport. The resulting data ...

  11. A Hybrid Approach for Estimating Total Deposition in the ...

    EPA Pesticide Factsheets

    Atmospheric deposition of nitrogen and sulfur causes many deleterious effects on ecosystems including acidification and excess eutrophication. Assessments to support development of strategies to mitigate these effects require spatially and temporally continuous values of nitrogen and sulfur deposition. In the U.S., national monitoring networks exist that provide values of wet and dry deposition at discrete locations. While wet deposition can be interpolated between the monitoring locations, dry deposition cannot. Additionally, monitoring networks do not measure the complete suite of chemicals that contribute to total sulfur and nitrogen deposition. Regional air quality models provide spatially continuous values of deposition of monitored species as well as important unmeasured species. However, air quality modeling values are not generally available for an extended continuous time period. Air quality modeling results may also be biased for some chemical species. We developed a novel approach for estimating dry deposition using data from monitoring networks such as the Clean Air Status and Trends Network (CASTNET), the National Atmospheric Deposition Program (NADP) Ammonia Monitoring Network (AMoN), and the Southeastern Aerosol Research and Characterization (SEARCH) network and modeled data from the Community Multiscale Air Quality (CMAQ) model. These dry deposition values estimates are then combined with wet deposition values from the NADP National Trends Networ

  12. A Novel Hybrid Approach for Estimating Total Deposition in ...

    EPA Pesticide Factsheets

    Atmospheric deposition of nitrogen and sulfur causes many deleterious effects on ecosystems including acidification and excess eutrophication. Assessments to support development of strategies to mitigate these effects require spatially and temporally continuous values of nitrogen and sulfur deposition. In the U.S., national monitoring networks exist that provide values of wet and dry deposition at discrete locations. While wet deposition can be interpolated between the monitoring locations, dry deposition cannot. Additionally, monitoring networks do not measure the complete suite of chemicals that contribute to total sulfur and nitrogen deposition. Regional air quality models provide spatially continuous values of deposition of monitored species as well as important unmeasured species. However, air quality modeling values are not generally available for an extended continuous time period. Air quality modeling results may also be biased for some chemical species. We developed a novel approach for estimating dry deposition using data from monitoring networks such as the Clean Air Status and Trends Network (CASTNET), the National Atmospheric Deposition Program (NADP) Ammonia Monitoring Network (AMoN), and the Southeastern Aerosol Research and Characterization (SEARCH) network and modeled data from the Community Multiscale Air Quality (CMAQ) model. These dry deposition values estimates are then combined with wet deposition values from the NADP National Trends Networ

  13. Seismic stratigraphy and depositional history of late Quaternary deposits at the eastern Yellow Sea shelf

    NASA Astrophysics Data System (ADS)

    Yoo, Dong-Geun; Lee, Gwang-Soo; Kim, Gil-Young; Chang, Se-Won; Kim, Kyoung-Jin

    2017-04-01

    The late Quaternary stratigraphy and sedimentation at the eastern Yellow Sea shelf was studied using a dense network of high-resolution, single-channel seismic reflection profiles and sediment data. The shelf sequence in this area consists of six seismic units formed since the LGM. During the LGM, the study area was completely exposed, resulting in subaerial erosion associated with paleo-channel incision by the Huanghe and Korean Rivers. As the shelf was flooded, the incised channels were backfilled fluvial or coastal sediments, forming incised channel-fill deposits (SU1). The paleo-river may have supplied abundant terrigenous sediments to the study area around the paleo-river mouth and adjacent area. These sediments were trapped within the paleo-estuary and formed SU2, regarded as an estuarine deposit. Two types of serial sand ridges (SU3 and SU5) which correspond to transgressive deposits developed. SU3 on the southern part, west of Jeju Island (80 110 m deep) is regarded as a moribund-type mainly formed during the early to middle stage of transgression. These are thought to have ceased growing and remobilizing. In contrast, SU5 (occurring 30 50 m deep off the Korean Peninsula) is generally regarded as active sand ridges deposited during the late stage of transgression and is partly modified by modern tidal currents. As the transgression continued, the near-surface sediments were reworked and redistributed by shelf erosion, resulting in a thin veneer of transgressive sands (SU4). The uppermost unit (SU6) formed the Heuksan Mud Belt (HMB), which is one of the most prominent mud deposits in the Yellow Sea. The lower part of the HMD corresponds to shelf-mud deposited during the late stage of transgression, whereas the upper part consists of a recent shelf-delta developed after the highstand sea level at about 7 ka BP.

  14. Annealing-Based Electrical Tuning of Cobalt-Carbon Deposits Grown by Focused-Electron-Beam-Induced Deposition.

    PubMed

    Puydinger Dos Santos, Marcos V; Velo, Murilo F; Domingos, Renan D; Zhang, Yucheng; Maeder, Xavier; Guerra-Nuñez, Carlos; Best, James P; Béron, Fanny; Pirota, Kleber R; Moshkalev, Stanislav; Diniz, José A; Utke, Ivo

    2016-11-30

    An effective postgrowth electrical tuning, via an oxygen releasing method, to enhance the content of non-noble metals in deposits directly written with gas-assisted focused-electron-beam-induced deposition (FEBID) is presented. It represents a novel and reproducible method for improving the electrical transport properties of Co-C deposits. The metal content and electrical properties of Co-C-O nanodeposits obtained by electron-induced dissociation of volatile Co 2 (CO) 8 precursor adsorbate molecules were reproducibly tuned by applying postgrowth annealing processes at 100 °C, 200 °C, and 300 °C under high-vacuum for 10 min. Advanced thin film EDX analysis showed that during the annealing process predominantly oxygen is released from the Co-C-O deposits, yielding an atomic ratio of Co:C:O = 100:16:1 (85:14:1) with respect to the atomic composition of as-written Co:C:O = 100:21:28 (67:14:19). In-depth Raman analysis suggests that the amorphous carbon contained in the as-written deposit turns into graphite nanocrystals with size of about 22.4 nm with annealing temperature. Remarkably, these microstructural changes allow for tuning of the electrical resistivity of the deposits over 3 orders of magnitude from 26 mΩ cm down to 26 μΩ cm, achieving a residual resistivity of ρ 2K /ρ 300 K = 0.56, close to the value of 0.53 for pure Co films with similar dimensions, making it especially interesting and advantageous over the numerous works already published for applications such as advanced scanning-probe systems, magnetic memory, storage, and ferroelectric tunnel junction memristors, as the graphitic matrix protects the cobalt from being oxidized under an ambient atmosphere.

  15. Dust and Ice Deposition in the Martian Geologic Record

    USGS Publications Warehouse

    Tanaka, K.L.

    2000-01-01

    The polar layered deposits of Mars demonstrate that thick accumulations of dust and ice deposits can develop on the planet if environmental conditions are favorable. These deposits appear to be hundreds of millions of years old, and other deposits of similar size but of greater age in nonpolar regions may have formed by similar processes. Possible relict dust deposits include, from oldest to youngest: Noachian intercrater materials, including Arabia mantle deposits, Noachian to Early Hesperian south polar pitted deposits, Early Hesperian Hellas and Argyre basin deposits, Late Hesperian Electris deposits, and the Amazonian Medusae Fossae Formation. These deposits typically are hundreds of meters to a couple kilometers thick and cover upward of a million or more square kilometers. The apparent persistence of dust sedimentation at the south pole back to the Early Hesperian or earlier and the early growth of Tharsis during the Late Noachian and perhaps earlier indicates that extensive polar wandering is unlikely following the Middle Noachian. A scenario for the overall history of dust and perhaps ice deposition on Mars includes widespread, voluminous accumulations perhaps planetwide during the Noachian as impacts, volcanism, and surface processes generated large amounts of dust; the Arabia deposits may have formed as ice availability and dust accumulation waned. During the Early Hesperian, thick dust sedimentation became restricted to the south pole and the deep Hellas and Argyre basins; the north polar sedimentary record prior to the Amazonian is largely obscured. Deposits at Electris and Medusae Fossae may have resulted from local sources of fine-grained material - perhaps volcanic eruptions.

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