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Sample records for rapid lead isotope

  1. Rapid lead isotope analysis of archaeological metals by multiple-collector inductively coupled plasma mass spectrometry

    DEFF Research Database (Denmark)

    Baker, J.A.; Stos, S.; Waight, Tod Earle

    2006-01-01

    Lead isotope ratios in archaeological silver and copper were determined by MC-ICPMS using laser ablation and bulk dissolution without lead purification. Laser ablation results on high-lead metals and bulk solution analyses on all samples agree within error of TIMS data, suggesting that problems...... from isobaric interferences and/or mass bias variations due to the presence of matrix elements are insignificant. Inaccurate laser ablation analyses on low-lead copper reflect erroneous mass bias corrections from use of a non-matrix matched standard. However, in most cases, silver and copper...... are analysable for lead isotopes by bulk dissolution or laser ablation MC-ICPMS with simplified sample preparation....

  2. Rapid Lead Screening Test

    Science.gov (United States)

    ... Vitro Diagnostics Tests Used In Clinical Care Rapid Lead Screening Test Share Tweet Linkedin Pin it More ... reducing the need for a follow-up visit. Lead Risk Links Centers for Disease Control and Prevention ( ...

  3. Lead Isotopes in Highway Runoff

    Science.gov (United States)

    Ferreira, M.; Lau, S.; Green, P. G.; Stenstrom, M. K.

    2011-12-01

    Lead (Pb) isotopes have been used extensively to study the provenance of lead pollution on air, water, and sediments. In this study, we measured Pb isotopes and Pb aqueous concentration in highway runoff in three west Los Angeles sites. Those three sites, part of a long-term study sponsored by the California Department of Transportation, represent small catchment areas, and host heavy traffic. In addition, there were no inputs of sand or salt to the highway because the sites are almost completely impervious and also due to the lack of snow to be controlled. Highway runoff from the three sites was collected for 7 storms during the 2004-2005 Winter. Grab samples were collected every 15 minutes during the first hour, and hourly afterwards. A total of 202 samples were collected and filtered into five size fractions (100μm). Aqueous concentration of Pb range from 0.08μg/L to 46.95μg/L (7.98±10.89μg/L) and it is not correlated with any of the lead isotope ratios. The 208Pb/206Pb ratio ranges from 1.983 to 2.075 (2.024±0.026) and there is no statistical difference for the mean value of the 208Pb/206Pb ratio for the four particulate size fractions (0.45-8μm, 8-20μm, 20-100μm, >100μm). However, the 208Pb/206Pb ratio of nearby soils yield 2.060±0.021 and it is statistically different from the ratios obtained for the highway runoff. This hints that the lead present in highway runoff does not come from local soils. The 207Pb/206Pb ratio ranges from 0.804 to 0.847 (0.827±0.011) and there is no statistical difference for the mean value of the 207Pb/206Pb ratio for the four particulate size fractions (0.45-8μm, 8-20μm, 20-100μm, >100μm). Surprisingly, there is also no statistical difference with the 207Pb/206Pb ratio of nearby soils (0.833±0.009).

  4. Lead isotopes as a supplementary tool in the routine evaluation of household lead hazards.

    OpenAIRE

    Gwiazda, R H; Smith, D. R.

    2000-01-01

    The advent of magnetic sector inductively coupled plasma-mass spectrometry (ICP-MS) allows rapid, accurate, and precise measurement of lead isotopes in environmental and biological samples at a lower cost than traditional methods. This may increase the feasibility of including lead isotope measurements as a routine tool to identify household sources of lead exposure to children. Here, we present three household case studies to illustrate how lead hazard evaluations by an environmental special...

  5. Worldwide lead-isotope ratio in bivalves and sediments

    DEFF Research Database (Denmark)

    Larsen, Martin Mørk; Jacobsen, Gitte; Strand, Jakob

    The lead-isotope ratio have been used to assess and identify impact of leaded gasoline, coal combustion and  mineral activities[ref 1] due to the difference in 206Pb (~52%), 207Pb (~24%) and 208Pb (~23%) isotope ratios. The source of these differences is the decaying of the parent isotopes of 238U...

  6. Discovery of the thallium, lead, bismuth, and polonium isotopes

    Science.gov (United States)

    Fry, C.; Thoennessen, M.

    2013-05-01

    Forty-two thallium, forty-two lead, forty-one bismuth, and forty-two polonium isotopes have so far been observed; the discovery of these isotopes is described. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  7. Discovery of the thallium, lead, bismuth, and polonium isotopes

    CERN Document Server

    Fry, C

    2012-01-01

    Currently, forty-two thallium, forty-two lead, forty-one bismuth, and forty-two polonium isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

  8. Historical record of lead accumulation and source in the tidal flat of Haizhou Bay, Yellow Sea: Insights from lead isotopes.

    Science.gov (United States)

    Zhang, Rui; Guan, Minglei; Shu, Yujie; Shen, Liya; Chen, Xixi; Zhang, Fan; Li, Tiegang

    2016-05-15

    In order to investigate the historical records of lead contamination and source in coastal region of Haizhou Bay, Yellow Sea, a sediment core was collected from tidal flat, dated by (210)Pb and (137)Cs. Lead and its stable isotopic ratios were determined. The profiles of enrichment factor (EF) and Pb isotope ratios showed increasing trend upward throughout the core, correlating closely with the experience of a rapid economic and industrial development of the catchment. According to Pb isotopic ratios, coal combustion emission mainly contributed to the Pb burden in sediments. Based on end-member model, coal combustion emission dominated anthropogenic Pb sources in recent decades contributing from 48% to 67% in sediment. And the contribution of leaded gasoline was lower than 20%. A stable increase of coal combustion source was found in sediment core, while the contribution of leaded gasoline had declined recently, with the phase-out of leaded gasoline in China.

  9. Tables for determining lead, uranium, and thorium isotope ages

    Science.gov (United States)

    Schonfeld, E.

    1974-01-01

    Tables for determining lead, uranium, and thorium isotope ages are presented in the form of computer printouts. Decay constants, analytical expressions for the functions evaluated, and the precision of the calculations are briefly discussed.

  10. Stable lead isotopic analyses of historic and contemporary lead contamination of San Francisco Bay estuary

    Science.gov (United States)

    Ritson, P.I.; Bouse, R.M.; Flegal, A.R.; Luoma, S.N.

    1999-01-01

    Variations in stable lead isotopic composition (240Pb, 206Pb, 207Pb, 208Pb) in three sediment cores from the San Francisco Bay estuary document temporal changes in sources of lead during the past two centuries. Sediment, with lead from natural geologic sources, and relatively homogeneous lead isotopic compositions are overlain by sediments whose isotopic compositions indicate change in the sources of lead associated with anthropogenic modification of the estuary. The first perturbations of lead isotopic composition in the cores occur in the late 1800s concordant with the beginning of industrialization around the estuary. Large isotopic shifts, toward lower 206Pb/207Pb, occur after the turn of the century in both Richardson and San Pablo Bays. A similar relationship among lead isotopic compositions and lead concentrations in both Bays suggest contamination from the same source (a lead smelter). The uppermost sediments (post 1980) of all cores also have a relatively homogenous lead isotopic composition distinct from pre-anthropogenic and recent aerosol signatures. Lead isotopic compositions of leachates from fourteen surface sediments and five marsh samples from the estuary were also analyzed. These analyses suggest that the lead isotopic signature identified in the upper horizons of the cores is spatially homogeneous among recently deposited sediments throughout the estuary. Current aerosol lead isotopic compositions [Smith, D.R., Niemeyer, S., Flegal, A.R., 1992. Lead sources to California sea otters: industrial inputs circumvent natural lead biodepletion mechanisms. Environmental Research 57, 163-175] are distinct from the isotopic compositions of the surface sediments, suggesting that the major source of lead is cycling of historically contaminated sediments back through the water column. Both the upper core sediments and surface sediments apparently derive their lead predominantly from sources internal to the estuary. These results support the idea that

  11. The identification of lead ammunition as a source of lead exposure in First Nations: The use of lead isotope ratios

    Energy Technology Data Exchange (ETDEWEB)

    Tsuji, Leonard J.S. [Department of Environment and Resource Studies, University of Waterloo, Waterloo, Ontario, N2L 3G1 (Canada)], E-mail: ljtsuji@fes.uwaterloo.ca; Wainman, Bruce C. [Faculty of Health Sciences, McMaster University, Hamilton, Ontario, L8N 3Z5 (Canada); Martin, Ian D. [Department of Environment and Resource Studies, University of Waterloo, Waterloo, Ontario, N2L 3G1 (Canada); Sutherland, Celine [Attawapiskat First Nation Health Services, Attawapiskat, Ontario, P0L 1A0 (Canada); Weber, Jean-Philippe; Dumas, Pierre [Centre de toxicologie, Institut national de sante publique du Quebec, Quebec City, Quebec, G1V 5B3 (Canada); Nieboer, Evert [Faculty of Health Sciences, McMaster University, Hamilton, Ontario, L8N 3Z5 (Canada); Institute of Community Medicine, University of Tromso, Tromso N-9037 (Norway)

    2008-04-15

    The use of lead shotshell to hunt water birds has been associated with lead-contamination in game meat. However, evidence illustrating that lead shotshell is a source of lead exposure in subsistence hunting groups cannot be deemed definitive. This study seeks to determine whether lead shotshell constitutes a source of lead exposure using lead isotope ratios. We examined stable lead isotope ratios for lichens, lead shotshell and bullets, and blood from residents of Fort Albany and Kashechewan First Nations, and the City of Hamilton, Ontario, Canada. Data were analyzed using ANOVA and regression analyses. ANOVA of isotope ratios for blood revealed significant differences with respect to location, but not sex. Hamilton differed from both Kashechewan and Fort Albany; however, the First Nations did not differ from each other. ANOVA of the isotope ratios for lead ammunition and lichens revealed no significant differences between lichen groups (north and south) and for the lead ammunition sources (pellets and bullets). A plot of {sup 206}Pb/{sup 204}Pb and {sup 206}Pb/{sup 207}Pb values illustrated that lichens and lead ammunition were distinct groupings and only the 95% confidence ellipse of the First Nations group overlapped that of lead ammunition. In addition, partial correlations between blood-lead levels (adjusted for age) and isotope ratios revealed significant (p < 0.05) positive correlations for {sup 206}Pb/{sup 204}Pb and {sup 206}Pb/{sup 207}Pb, and a significant negative correlation for {sup 208}Pb/{sup 206}Pb, as predicted if leaded ammunition were the source of lead exposure. In conclusion, lead ammunition was identified as a source of lead exposure for First Nations people; however, the isotope ratios for lead shotshell pellets and bullets were indistinguishable. Thus, lead-contaminated meat from game harvested with lead bullets may also be contributing to the lead body burden.

  12. The identification of lead ammunition as a source of lead exposure in First Nations: the use of lead isotope ratios.

    Science.gov (United States)

    Tsuji, Leonard J S; Wainman, Bruce C; Martin, Ian D; Sutherland, Celine; Weber, Jean-Philippe; Dumas, Pierre; Nieboer, Evert

    2008-04-15

    The use of lead shotshell to hunt water birds has been associated with lead-contamination in game meat. However, evidence illustrating that lead shotshell is a source of lead exposure in subsistence hunting groups cannot be deemed definitive. This study seeks to determine whether lead shotshell constitutes a source of lead exposure using lead isotope ratios. We examined stable lead isotope ratios for lichens, lead shotshell and bullets, and blood from residents of Fort Albany and Kashechewan First Nations, and the City of Hamilton, Ontario, Canada. Data were analyzed using ANOVA and regression analyses. ANOVA of isotope ratios for blood revealed significant differences with respect to location, but not sex. Hamilton differed from both Kashechewan and Fort Albany; however, the First Nations did not differ from each other. ANOVA of the isotope ratios for lead ammunition and lichens revealed no significant differences between lichen groups (north and south) and for the lead ammunition sources (pellets and bullets). A plot of (206)Pb/(204)Pb and (206)Pb/(207)Pb values illustrated that lichens and lead ammunition were distinct groupings and only the 95% confidence ellipse of the First Nations group overlapped that of lead ammunition. In addition, partial correlations between blood-lead levels (adjusted for age) and isotope ratios revealed significant (pleaded ammunition were the source of lead exposure. In conclusion, lead ammunition was identified as a source of lead exposure for First Nations people; however, the isotope ratios for lead shotshell pellets and bullets were indistinguishable. Thus, lead-contaminated meat from game harvested with lead bullets may also be contributing to the lead body burden.

  13. Tracing source pollution in soils using cadmium and lead isotopes.

    Science.gov (United States)

    Cloquet, C; Carignan, J; Libourel, G; Sterckeman, T; Perdrix, E

    2006-04-15

    Tracing the source of heavy metals in the environment is of key importance for our understanding of their pollution and natural cycles in the surface Earth reservoirs. Up to now, most exclusively Pb isotopes were used to effectively trace metal pollution sources in the environment. Here we report systematic variations of Cd isotope ratios measured in polluted topsoils surrounding a Pb-Zn refinery plant in northern France. Fractionated Cd was measured in soil samples surrounding the refinery, and this fractionation can be attributed to the refining processes. Despite the Cd isotopic ratios being precisely measured, the obtained uncertainties are still large compared to the total isotopic variation. Nevertheless, for the first time, Cd isotopically fractionated by industrial processes may be traced in the environment. On the same samples, Pb isotope systematics suggested that materials actually used by the refinery were not the major source of Pb in soils, probably because refined ore origins changed over the 100 years of operation. On the other hand, Cd isotopes and concentrations measured in topsoils allowed identification of three main origins (industrial dust and slag and agriculture), assuming that all Cd ores are not fractionated, as suggested by terrestrial rocks so far analyzed, and calculation of their relative contributions for each sampling point. Understanding that this refinery context was an ideal situation for such a study, our results lead to the possibility of tracing sources of anthropogenic Cd and better constrain mixing processes, fluxes, transport, and phasing out of industrial input in nature.

  14. Worldwide lead-isotope ratio in bivalves and sediments

    DEFF Research Database (Denmark)

    Larsen, Martin Mørk; Jacobsen, Gitte; Strand, Jakob

    The lead-isotope ratio have been used to assess and identify impact of leaded gasoline, coal combustion and  mineral activities[ref 1] due to the difference in 206Pb (~52%), 207Pb (~24%) and 208Pb (~23%) isotope ratios. The source of these differences is the decaying of the parent isotopes of 238U...... to 206Pb, 235U to 207Pb and 232Th to 208Pb. 204Pb is the only stable Pb isotope usually contributing 1% of the total Pb. Differences in 206Pb/207Pb ratio ranges from 1.06 to 1.10 in old Pb ores (e.g. the time of the roman empire), whereas recent mining from radiogenic (high U and Th contents) ores can.......35% with recoveries of  98.50 to 100.03%. Geographical differences and comparison with literature values for the different regions will be presented, together with a discussion on the suitability of ICP-quadropole-MS for isotope ratio determinations. ...

  15. Monitoring steel bridge renovation using lead isotopic tracing.

    Science.gov (United States)

    Salome, Fred; Gulson, Brian; Chiaradia, Massimo; Davis, Jeffrey; Morris, Howard

    2017-05-01

    Monitoring removal of lead (Pb) paint from steel structures usually involves analysis of environmental samples for total lead and determination of blood Pb levels of employees involved in the Pb paint removal. We used high precision Pb isotopic tracing for a bridge undergoing Pb paint removal to determine if Pb in the environmental and blood samples originated from the bridge paint. The paint system on the bridge consisted of an anti-corrosive red Pb primer top-coated with a Micaceous Iron Oxide (MIO) alkyd. Analysis of the red Pb primer gave uniform isotopic ratios indicative of Pb from the geologically-ancient Broken Hill mines in western New South Wales, Australia. Likewise waste abrasive material, as anticipated, had the same isotopic composition as the paint. The isotopic ratios for other samples lay on 2 separate linear arrays on a(207)Pb/(204)Pb versus (206)Pb/(204)Pb diagram, one largely defined by gasoline and the majority of the ambient air data, and the other by data for one sample each of gasoline and ambient air and underwater sediments. Isotopic ratios in background ambient air samples for the project were characteristic of leaded gasoline. Air sampling during paint removal showed a contribution of paint Pb ranging from about 20 to 40%. Isotopic ratios in the blood of 8 employees prior to the commencement of work showed that 6 of these had been previously exposed to the Broken Hill Pb possibly from earlier bridge paint removal projects. One subject appeared to have increased exposure to Pb probably from the paint renovations.

  16. Lead Isotope Characterization of Petroleum Fuels in Taipei, Taiwan

    Directory of Open Access Journals (Sweden)

    Pei-Hsuan Yao

    2015-04-01

    Full Text Available Leaded gasoline in Taiwan was gradually phased out from 1983 to 2000. However, it is unclear whether unleaded gasoline still contributes to atmospheric lead (Pb exposure in urban areas. In this study, Pb isotopic compositions of unleaded gasolines, with octane numbers of 92, 95, 98, and diesel from two local suppliers in Taipei were determined by multi-collector inductively coupled plasma mass spectrometry with a two-sigma uncertainty of ± 0.02 %. Lead isotopic ratios of vehicle exhaust (208Pb/207Pb: 2.427, 206Pb/207Pb: 1.148, as estimated from petroleum fuels overlap with the reported aerosol data. This agreement indicates that local unleaded petroleum fuels, containing 10–45 ng·Pb·g−1, are merely one contributor among various sources to urban aerosol Pb. Additionally, the distinction between the products of the two companies is statistically significant in their individual 208Pb/206Pb ratios (p-value < 0.001, t test. Lead isotopic characterization appears to be applicable as a “fingerprinting” tool for tracing the sources of Pb pollution.

  17. Tracing changes in atmospheric sources of lead contamination using lead isotopic compositions in Australian red wine.

    Science.gov (United States)

    Kristensen, Louise Jane; Taylor, Mark Patrick; Evans, Andrew James

    2016-07-01

    Air quality data detailing changes to atmospheric composition from Australia's leaded petrol consumption is spatially and temporally limited. In order to address this data gap, wine was investigated as a potential proxy for atmospheric lead conditions. Wine spanning sixty years was collected from two wine regions proximal to the South Australian capital city, Adelaide, and analysed for lead concentration and lead and strontium isotopic composition for source apportionment. Maximum wine lead concentrations (328 μg/L) occur prior to the lead-in-air monitoring in South Australia in the later 1970s. Wine lead concentrations mirror available lead-in-air measurements and show a declining trend reflecting parallel reductions in leaded petrol emissions. Lead from petrol dominated the lead in wine ((206)Pb/(207)Pb: 1.086; (208)Pb/(207)Pb: 2.360) until the introduction of unleaded petrol, which resulted in a shift in the wine lead isotopic composition closer to vineyard soil ((206)Pb/(207)Pb: 1.137; (208)Pb/(207)Pb: 2.421). Current mining activities or vinification processes appear to have no impact with recent wine samples containing less than 4 μg/L of lead. This study demonstrates wine can be used to chronicle changes in environmental lead emissions and is an effective proxy for atmospherically sourced depositions of lead in the absence of air quality data.

  18. Lead isotope ratios as a tracer for lead contamination sources: A lake Andong case study

    Directory of Open Access Journals (Sweden)

    Kim Y. H

    2013-04-01

    Full Text Available The objective of this study was to evaluate stable Pb isotope signatures as a tracer for Pb contamination in Lake Andong. For Pb isotope analysis, we collected water and sediment from Lake Andong, particles in the air, soils, and stream water, mine tailings, sludge and wastewater from zinc smelting around lake Andong watershed. The results showed that Pb isotope ratios (206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb for zinc concentrate were 18.809 ± 0.322, 15.650 ± 0.062, and 38.728 ± 0.421, respectively. In wastewater, isotopic ratio values (206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb were 17.363 ± 0.133, 15.550 ± 0.025, and 37.217 ± 0.092, respectively. Additionally, isotopic ratio values (206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb for sludge were 17.515 ± 0.155, 15.537 ± 0.018, and 37.357 ± 0.173, respectively. These values were similar to those in zinc and lead concentrate originated from Canada and South America. In contrast, Pb isotope ratios of soil, tailings and sediment from Lake Andong were similar to those of Korean ore. Atmospheric particles showed different patterns of Pb isotope ratios from sediments, soils, and zinc smelting and this needs further investigation in order to identify atmospheric Pb sources.

  19. Intruder bands and configuration mixing in the lead isotopes

    OpenAIRE

    Fossion, R.; Heyde, K.; Thiamova, G.; Van Isacker, P.(GANIL, CEA/DSM–CNRS/IN2P3, Bd Henri Becquerel, BP 55027, F-14076 Caen Cedex 5, France)

    2003-01-01

    A three-configuration mixing calculation is performed in the context of the interacting boson model with the aim to describe recently observed collective bands built on low-lying $0^+$ states in neutron-deficient lead isotopes. The configurations that are included correspond to the regular, spherical states as well as two-particle two-hole and four-particle four-hole excitations across the Z=82 shell gap.

  20. Lead isotopes in soils near five historic American lead smelters and refineries.

    Science.gov (United States)

    Rabinowitz, Michael B

    2005-06-15

    This survey of soil lead in the vicinity of old industrial sites examines how the stable isotope patterns vary among the sites according to the sources of the lead ore processed at each site. Lead smelters and refineries, which closed down decades ago, are the basis of this investigation. Samples were taken from near five old factory sites in Collinsville and Alton (Illinois), Ponderay (Idaho), East Chicago (Indiana) and Omaha (Nebraska). Historical records were searched for accounts of the sources of the lead. Lead concentrations were measured by atomic absorption flame spectrophotometry, and stable isotopic analysis was done by plasma ionization mass spectrometry. At every site visited, remnants of the old factories, in terms of soil lead pollution, could be found. In spite of potential complications of varying smelter feedstock sourced from mines of different geological age, it was possible to match the isotopic patterns in the soils with the documented sources of the ores. The Collinsville and Alton sites resembled Missouri lead. The Ponderay value was higher than major Bunker Hill, Idaho deposits, but closer to the minor, nearby Oreille County, Washington ores. Mostly Utah ore was used in East Chicago. The Omaha soil reflects lead from Mexico, Colorado and Montana.

  1. Lead isotopes and trace metals in dust at Yucca Mountain

    Science.gov (United States)

    Kwak, Loretta; Neymark, Leonid A.; Peterman, Zell E.

    2008-01-01

    Lead (Pb)-isotope compositions and trace-metal concentrations were determined for samples of dust collected from underground and surface locations at and near the proposed radioactive waste repository at Yucca Mountain, Nevada. Rare earth element concentrations in the dust samples from the underground tunnels are similar to those in wholerock samples of the repository host rocks (Miocene Tiva Canyon Tuff and Topopah Spring Tuff), supporting interpretation that the subsurface dust is mainly composed of rock comminuted during tunnel construction. Other trace metals (arsenic, cadmium, cobalt, chromium, copper, manganese, nickel, lead, antimony, thallium, and zinc) are variably enriched in the subsurface dust samples relative to the average concentrations in the host rocks. Average concentrations of arsenic and lead in dust samples, high concentrations of which can cause corrosion of waste canisters, have enrichment factors from 1.2 to 1.6 and are insignificant relative to the range of concentrations for these metals observed in the host rock samples. Most dust samples from surface sites also are enriched in many of these trace metals relative to average repository host rocks. At least some of these enrichments may be artifacts of sampling. Plotted on a 208Pb/206Pb-207Pb/206Pb graph, Pb-isotope compositions of dust samples from underground sites form a mixing line extending from host-rock Pb-isotope compositions towards compositions of many of the dust samples from surface sites; however, combined Pb concentration and isotope data indicate the presence of a Pbenriched component in the subsurface dust that is not derived from host rock or surface dust and may derive from anthropogenic materials introduced into the underground environment.

  2. Lead sources and transfer in the coastal Mediterranean: evidence from stable lead isotopes in marine particles

    Science.gov (United States)

    Alleman, L. Y.; Hamelin, B.; Véron, A. J.; Miquel, J.-C.; Heussner, S.

    Time series of settling and suspended particles have been collected by sediment traps and in situ pumps respectively, under contrasted hydrographic conditions in the Gulf of Lions and the Ligurian Sea, northwestern Mediterranean. Lead concentrations measured in sediment trap samples vary from 41±7 ppm in the Ligurian Sea to 58±10 ppm in the Gulf of Lions. These concentrations, 2-10 times lower than those measured previously in the Gulf of Lions, reflect the reduction of lead fallout from gasoline during the last decade. While atmospheric lead still originates mainly from anthropogenic emissions (automotive and industrial exhausts), stable lead isotopes demonstrate that anthropogenic and lithogenic lead are in similar proportions in the marine particles from the northwestern Mediterranean. Sequential extraction analyses performed on trap samples suggest that the isotopic variations can be explained by a three-component mixing between anthropogenic, natural soluble, and natural refractory sources. In the suspended particulate matter from the Gulf of Lions, lead concentrations range from 0.2 to 30 ng/ l, with isotopic compositions comparable to those of the settling particles ( 206Pb/ 207Pb from 1.165 to 1.178). This indicates a common origin in these two types of particles, probably mainly controlled by the Rhône River discharge and by resuspension processes on the continental shelf. By contrast, lead concentrations are lower in the suspended matter samples from the Ligurian Sea (0.5 to 1.7 ng/ l). In this case, the isotopic signature (1.165±0.002) is in equilibrium with the dissolved fraction, as previously found in other oligotrophic sites in the open ocean, where the suspended particles are mainly of biological origin and lead essentially authigenic in these particles.

  3. Laser photochemical lead isotopes separation for harmless nuclear power engineering

    Science.gov (United States)

    Bokhan, P. A.; Fateev, N. V.; Kim, V. A.; Zakrevsky, D. E.

    2016-09-01

    The collisional quenching of the metastable 3 P 1,2 and 1 D 2 lead atoms is studied experimentally in the gas flow of the lead atoms, reagent-molecules and a carrier gas Ar. The experimental parameters were similar to the conditions that are required in the operation of the experimental setup for photochemical isotope separation. Excited atoms are generated under electron impact conditions created by a gas glow discharge through the mixture of gases and monitored photoelectrically by attenuation of atomic resonance radiation from hollow cathode 208Pb lamp. The decay of the excited atoms has been studied in the presence various molecules and total cross section data are reported. The flow tube measurements has allowed to separate the physical and chemical quenching channels and measure the rates of the chemical reaction excited lead with N2O, CH2Cl2, SF6 and CuBr molecules. These results are discussed in the prospects of the obtaining isotopically modified lead as a promising coolant in the reactors on the fast-neutron.

  4. Australian atmospheric lead deposition reconstructed using lead concentrations and isotopic compositions of archival lichen and fungi.

    Science.gov (United States)

    Wu, Liqin; Taylor, Mark Patrick; Handley, Heather K; Wu, Michael

    2016-01-01

    Lead concentrations and their isotopic compositions were measured in lichen genera Cladonia and Usnea and fungi genus Trametes from the Greater Sydney region (New South Wales, Australia) that had been collected and archived over the past 120 years. The median lead contents were elevated in lichens and fungi prior to the introduction of leaded petrol (Cladonia 12.5 mg/kg; Usnea 15.6 mg/kg; Trametes 1.85 mg/kg) corresponding to early industrial development. During the use of leaded petrol for automobiles in Australia from 1932 to 2002, total median lead concentrations rose: Cladonia 18.8 mg/kg; Usnea 21.5 mg/kg; Trametes 4.3 mg/kg. Following the cessation of leaded petrol use, median total lead concentrations decreased sharply in the 2000s: Cladonia 4.8 mg/kg; Usnea 1.7 mg/kg. The lichen and fungi isotopic compositions reveal a significant decrease in (206)Pb/(207)Pb values from the end of 19th century to the 1970s. The following decades were characterised by lower allowable levels of lead additive in fuel and the introduction of unleaded petrol in 1985. The environmental response to these regulatory changes was that lichen and fungi (206)Pb/(207)Pb values increased, particularly from 1995 onwards. Although the lead isotope ratios of lichens continued to increase in the 2000s they do not return to pre-leaded petrol values. This demonstrates that historic leaded petrol emissions, inter alia other sources, remain a persistent source of anthropogenic contamination in the Greater Sydney region.

  5. A new method for stable lead isotope extraction from seawater

    Energy Technology Data Exchange (ETDEWEB)

    Zurbrick, Cheryl M., E-mail: CZurbric@ucsc.edu [WIGS, Department of Microbiology and Environmental Toxicology, University of California Santa Cruz, 1156 High Street, Santa Cruz, CA 95064 (United States); Gallon, Céline [Institute of Marine Sciences, University of California Santa Cruz, 1156 High Street, Santa Cruz, CA 95064 (United States); Flegal, A. Russell [WIGS, Department of Microbiology and Environmental Toxicology, University of California Santa Cruz, 1156 High Street, Santa Cruz, CA 95064 (United States); Institute of Marine Sciences, University of California Santa Cruz, 1156 High Street, Santa Cruz, CA 95064 (United States)

    2013-10-24

    Graphical abstract: -- Highlights: •We present a relatively fast (2.5–6.5 h), semi-automated system to extract Pb from seawater. •Extraction requires few chemicals and has a relatively low blank (0.7 pmol kg{sup −1}). •We compare analyses of Pb isotopes by HR ICP-MS with those by MC-ICP-MS. -- Abstract: A new technique for stable lead (Pb) isotope extraction from seawater is established using Toyopearl AF-Chelate 650 M{sup ®} resin (Tosoh Bioscience LLC). This new method is advantageous because it is semi-automated and relatively fast; in addition it introduces a relatively low blank by minimizing the volume of chemicals used in the extraction. Subsequent analyses by HR ICP-MS have a good relative external precision (2σ) of 3.5‰ for {sup 206}Pb/{sup 207}Pb, while analyses by MC-ICP-MS have a better relative external precision of 0.6‰. However, Pb sample concentrations limit MC-ICP-MS analyses to {sup 206}Pb, {sup 207}Pb, and {sup 208}Pb. The method was validated by processing the common Pb isotope reference material NIST SRM-981 and several GEOTRACES intercalibration samples, followed by analyses by HR ICP-MS, all of which showed good agreement with previously reported values.

  6. Heavy metals and lead isotopes in sdB stars

    CERN Document Server

    O'Toole, S

    2006-01-01

    We present a detailed abundance analysis of high-resolution ultraviolet echelle spectra of five subdwarf B stars obtained with HST-STIS The goal of our observations was to test the hypothesis that pulsations in sdBs are correlated to the surface abundances of iron-group elements. We study two pulsators and three non-pulsators and determined abundances for 25 elements including the iron group and even heavier elements such as tin and lead using LTE spectrum synthesis techniques. We find strong enrichments of heavy elements up to 2.9dex with respect to solar which are probably caused by atomic diffusion processes. No clear-cut correlation between pulsations and metal abundances becomes apparent. Abundances for lead isotopes are derived from very high resolution spectra using an UV line of triply ionised lead. As Pb terminates the s-process sequence Pb isotopic abundance ratios yield important constraints. It is very difficult to measure them in hot stars. For the first time we were able to measure them in two s...

  7. Lead contamination and transfer in urban environmental compartments analyzed by lead levels and isotopic compositions.

    Science.gov (United States)

    Hu, Xin; Sun, Yuanyuan; Ding, Zhuhong; Zhang, Yun; Wu, Jichun; Lian, Hongzhen; Wang, Tijian

    2014-04-01

    Lead levels and isotopic compositions in atmospheric particles (TSP and PM2.5), street dust and surface soil collected from Nanjing, a mega city in China, were analyzed to investigate the contamination and the transfer of lead in urban environmental compartments. The lead contents in TSP and PM2.5 are significantly higher than them in the surface soil and street dust (p atmospheric particles. The plots of (206)Pb/(207)Pb vs.(208)Pb/(206)Pb and (206)Pb/(207)Pb vs. 1/Pb imply that the street dust and atmospheric particles (TSP and PM2.5) have very similar lead sources. Coal emissions and smelting activities may be the important lead sources for street dust and atmospheric particles (TSP and PM2.5), while the deposition of airborne lead is an important lead source for urban surface soil.

  8. DEVELOPMENT OF LEAD SLOWING DOWN SPECTROMETER FOR ISOTOPIC FISSILE ASSAY

    Directory of Open Access Journals (Sweden)

    SANG JOON AHN

    2014-12-01

    Full Text Available A lead slowing down spectrometer (LSDS is under development for analysis of isotopic fissile material contents in pyro-processed material, or spent fuel. Many current commercial fissile assay technologies have a limitation in accurate and direct assay of fissile content. However, LSDS is very sensitive in distinguishing fissile fission signals from each isotope. A neutron spectrum analysis was conducted in the spectrometer and the energy resolution was investigated from 0.1eV to 100keV. The spectrum was well shaped in the slowing down energy. The resolution was enough to obtain each fissile from 0.2eV to 1keV. The detector existence in the lead will disturb the source neutron spectrum. It causes a change in resolution and peak amplitude. The intense source neutron production was designed for ∼E12 n's/sec to overcome spent fuel background. The detection sensitivity of U238 and Th232 fission chamber was investigated. The first and second layer detectors increase detection efficiency. Thorium also has a threshold property to detect the fast fission neutrons from fissile fission. However, the detection of Th232 is about 76% of that of U238. A linear detection model was set up over the slowing down neutron energy to obtain each fissile material content. The isotopic fissile assay using LSDS is applicable for the optimum design of spent fuel storage to maximize burnup credit and quality assurance of the recycled nuclear material for safety and economics. LSDS technology will contribute to the transparency and credibility of pyro-process using spent fuel, as internationally demanded.

  9. Variations in lead isotopic abundances in Sprague-Dawley rat tissues: possible reason of formation.

    Directory of Open Access Journals (Sweden)

    Duojian Liu

    Full Text Available It has been reported in previous research that the lead isotopic composition of blood, urine and feces samples statistically differed from the given lead sources in Sprague-Dawley (SD rats. However, the reason for this phenomenon is still unclear. An animal experiment was performed to investigate the lead isotope fractionation in diverse biological samples (i.e., lungs, liver, kidneys, bone and to explore the possible reasons. SD rats were intratracheally instilled with lead acetate at the concentrations of 0, 0.02, 0.2, and 2 mg/kg body weight. Biological samples were collected for lead isotope analysis using an inductively coupled plasma mass spectrometry (ICP-MS. Significant differences are observed in lead isotope abundances among the diverse biological samples. The lead isotope abundances ((206Pb, (207Pb and (208Pb in diverse biological samples show different degrees and directions of departure from the given lead source. The results suggest that differences in enrichment or depletion capacity for each lead isotope in the various tissues might lead to the variation in lead isotopic abundances in tissues. Moreover, a nonlinear relationship between the blood lead level and the lead isotope abundances in liver and bone is observed. When the whole-blood level is higher than 50 ng/mL, the lead isotopic compositions of biological samples tend to be the same. Thus, the data support the speculation of a fractionation functional threshold.

  10. Lead and zinc dust depositions from ore trains characterised using lead isotopic compositions.

    Science.gov (United States)

    Kristensen, L J; Taylor, M P; Morrison, A L

    2015-03-01

    This study investigates an unusual source of environmental lead contamination - the emission and deposition of lead and zinc concentrates along train lines into and out of Australia's oldest silver-lead-zinc mine at Broken Hill, Australia. Transport of lead and zinc ore concentrates from the Broken Hill mines has occurred for more than 125 years, during which time the majority was moved in uncovered rail wagons. A significant amount of ore was lost to the adjoining environments, resulting in soil immediately adjacent to train lines elevated with concentrations of lead (695 mg kg(-1)) and zinc (2230 mg kg(-1)). Concentrations of lead and zinc decreased away from the train line and also with depth shown in soil profiles. Lead isotopic compositions demonstrated the soil lead contained Broken Hill ore in increasing percentages closer to the train line, with up to 97% apportioned to the mined Broken Hill ore body. SEM examination showed ceiling dusts collected from houses along the train line were composed of unweathered galena particles, characteristic of the concentrate transported in the rail wagons. The loss of ore from the uncovered wagons has significantly extended the environmental footprint of contamination from local mining operations over an area extending hundreds of kilometres along each of the three train lines.

  11. Metallogeny and lead isotope data from the Oslo Paleorift

    Science.gov (United States)

    Bjørlykke, A.; Ihlen, P. M.; Olerud, S.

    1990-06-01

    The Permian Oslo Paleorift, situated at the southwestern margin of the Baltic shield, includes the Oslo Region and its southward extension under Skagerak. The exposed part of the paleorift comprises two half-grabens (Vestfold and Akershus graben segments) filled with Permian sediments, volcanics and intrusive rocks as well as Cambrc-Silurian sedimentary rocks. The evolution of the Oslo Rift can be divided into a rifting stage, a caldera stage and a batholith stage. The rifting stage is characterized by weak mineralization of native copper in basalts. The caldera stage includes Fe-Ti cumulates in subvolcanic layered alkali gabbros, Nb-REE disseminations in aphyric trachytes, and epigenetic Mo-mineralizations. The batholith stage includes porphyry and intraplutonic vein deposits of Mo and contact metasomatic deposits of Fe, W, Mo, Be, Zn, Pb, Cu, Bi, As and F. Along the rift margin in Precambrian gneisses and amphibolites there are vein deposits of Fe-oxides, base metals and native silver. The relationship between the rift margin deposits and the evolution of the rift is still unclear, but many deposits are spatially related to Permian dolerite dykes. Lead isotope data from hydrothermal deposits in the Oslo Rift fall into two main groups. The first group comprises the rift margin deposits. They are very radiogenic and reflect an upper crustal source for the metals. The source of the silver deposits generally has a lower μ-value and a higher w- value than the base metal deposits. The rift margin deposits are therefore not a product of metal zonation from a single hydrothermal solution. The second group comprises deposits associated with granitic intrusions in the Oslo Graben and reflects a lower to intermediate crustal source for the metals. Deposits in the Vestfold graben segment are generally more radiogenic than deposits in the Akershus graben segment and this difference may be explained by a small contribution of highly radiogenic lead from underlying Precambrian

  12. Rapid accurate isotopic measurements on boron in boric acid and boron carbide.

    Science.gov (United States)

    Duchateau, N L; Verbruggen, A; Hendrickx, F; De Bièvre, P

    1986-04-01

    A procedure is described whereby rapid and accurate isotopic measurements can be performed on boron in boric acid and boron carbide after fusion of these compounds with calcium carbonate. It allows the determination of the isotopic composition of boron in boric acid and boron carbide and the direct assay of boron or the (10)B isotope in boron carbide by isotope-dilution mass spectrometry.

  13. Identification of sources of lead exposure in French children by lead isotope analysis: a cross-sectional study

    Directory of Open Access Journals (Sweden)

    Lucas Jean-Paul

    2011-08-01

    Full Text Available Abstract Background The amount of lead in the environment has decreased significantly in recent years, and so did exposure. However, there is no known safe exposure level and, therefore, the exposure of children to lead, although low, remains a major public health issue. With the lower levels of exposure, it is becoming more difficult to identify lead sources and new approaches may be required for preventive action. This study assessed the usefulness of lead isotope ratios for identifying sources of lead using data from a nationwide sample of French children aged from six months to six years with blood lead levels ≥25 μg/L. Methods Blood samples were taken from 125 children, representing about 600,000 French children; environmental samples were taken from their homes and personal information was collected. Lead isotope ratios were determined using quadrupole ICP-MS (inductively coupled plasma - mass spectrometry and the isotopic signatures of potential sources of exposure were matched with those of blood in order to identify the most likely sources. Results In addition to the interpretation of lead concentrations, lead isotope ratios were potentially of use for 57% of children aged from six months to six years with blood lead level ≥ 25 μg/L (7% of overall children in France, about 332,000 children, with at least one potential source of lead and sufficiently well discriminated lead isotope ratios. Lead isotope ratios revealed a single suspected source of exposure for 32% of the subjects and were able to eliminate at least one unlikely source of exposure for 30% of the children. Conclusions In France, lead isotope ratios could provide valuable additional information in about a third of routine environmental investigations.

  14. Sargipali galenas: Unusual lead-isotope data from eastern India

    Science.gov (United States)

    Vishwakarma, Rajesh K.; Ulabhaje, A. V.

    1991-04-01

    The Sargipali sulphide deposit, hosted by a sequence of metasediments of the Precambrian Gangpur Series, represents the stratiform and stratabound Pb-Cu mineralization. Lead-isotope analyses obtained from six galena samples of different forms and stratigraphical levels, yielded a model Pb age of 1665 Ma, which predates the episodes of deformation and metamorphism (˜ 850 Ma) as well as syn-to late-tectonic magmatism. The model Pb age, on the contrary, shows a relationship to the closing phase of the Gangpur sedimentation (1700 Ma) in a shallow-water marine environment. The notable paucity of the interlayered volcanic rock in the deposit and its Pb-rich nature possibly point to its being the sedimentary exhalative (SEDEX) type. Documentary evidence for the Pb component from the geological environment of the “upper continental crust” is revealed by an exceptionally high μ(= 238U/204Pb) and the slightly above average W(= 232Th/238U) values. These indicate that the source rock was initially rich in U-Th-Pb concentration. For the Sargipali ore Pb, the parent is assumed to be late Archean-lower Proterozoic soda granite.

  15. Constraining recent lead pollution sources in the North Pacific using ice core stable lead isotopes

    Science.gov (United States)

    Gross, B. H.; Kreutz, K. J.; Osterberg, E. C.; McConnell, J. R.; Handley, M.; Wake, C. P.; Yalcin, K.

    2012-08-01

    Trends and sources of lead (Pb) aerosol pollution in the North Pacific rim of North America from 1850 to 2001 are investigated using a high-resolution (subannual to annual) ice core record recovered from Eclipse Icefield (3017 masl; St. Elias Mountains, Canada). Beginning in the early 1940s, increasing Pb concentration at Eclipse Icefield occurs coevally with anthropogenic Pb deposition in central Greenland, suggesting that North American Pb pollution may have been in part or wholly responsible in both regions. Isotopic ratios (208Pb/207Pb and 206Pb/207Pb) from 1970 to 2001 confirm that a portion of the Pb deposited at Eclipse Icefield is anthropogenic, and that it represents a variable mixture of East Asian (Chinese and Japanese) emissions transported eastward across the Pacific Ocean and a North American component resulting from transient meridional atmospheric flow. Based on comparison with source material Pb isotope ratios, Chinese and North American coal combustion have likely been the primary sources of Eclipse Icefield Pb over the 1970-2001 time period. The Eclipse Icefield Pb isotope composition also implies that the North Pacific mid-troposphere is not directly impacted by transpolar atmospheric flow from Europe. Annually averaged Pb concentrations in the Eclipse Icefield ice core record show no long-term trend during 1970-2001; however, increasing208Pb/207Pb and decreasing 206Pb/207Pb ratios reflect the progressive East Asian industrialization and increase in Asian pollutant outflow. The post-1970 decrease in North American Pb emissions is likely necessary to explain the Eclipse Icefield Pb concentration time series. When compared with low (lichen) and high (Mt. Logan ice core) elevation Pb data, the Eclipse ice core record suggests a gradual increase in pollutant deposition and stronger trans-Pacific Asian contribution with rising elevation in the mountains of the North Pacific rim.

  16. Using Lead Concentrations and Stable Lead Isotope Ratios to Identify Contamination Events in Alluvial Soils

    Directory of Open Access Journals (Sweden)

    Diane Saint-Laurent

    2010-01-01

    Full Text Available Soils contaminated with hydrocarbons (C10–C50, polycyclic aromatic hydrocarbons (PAHs, and other contaminants (e.g., As, Cd, Cu, Pb were recently discovered on the banks of the Saint-François and Massawippi rivers. Alluvial soils are contaminated over a distance of 100 kilometers, and the level of the contaminated-hydrocarbon layer in the soil profiles is among the highest at the Windsor and Richmond sites. Concentrations of lead and stable lead isotope ratios (204Pb/206Pb, 207Pb/206Pb, 208Pb/206Pb are also used to identify contamination events. The maximum and minimum values detected in soil profiles for arsenic, cadmium, and lead vary from 3.01 to 37.88 mg kg-1 (As, 0.11 to 0.81 mg kg-1 (Cd 12.32 to 149.13 mg kg-1 (Pb, respectively, while the 207Pb/206Pb isotopic ratio values are between 0.8545 and 0.8724 for all the profiles. The highest values of trace elements (As, Pb and Zn were detected in the hydrocarbon layer (C10–C50, most often located at the bottom of the profiles (160, 200, and 220 cm in depth. The various peaks recorded in the soils and the position of the profiles suggest that various contaminants were transported by the river on several occasions and infiltrated the soil matrix or deposited on floodplains during successive floods. Atmospheric particles which entered the river or deposited on riverbanks must also be considered as another source of pollution recorded in soils.

  17. Tracing the transport of anthropogenic lead in the atmosphere and in soils using isotopic ratios

    Science.gov (United States)

    Erel, Yigal; Veron, Alain; Halicz, Ludwik

    1997-11-01

    The isotopic composition of lead in aerosols and soils in Israel is used to characterize the sources of anthropogenic lead in the region, to ascertain the isotopic composition of natural, rock-derived lead in specific areas, and to determine rates of anthropogenic lead migration in soils. The isotopic composition of lead currently emitted from cars in Israel ( 206Pb /207Pb = 1.115 ± 2 ) is controlled by alkyl-lead produced in France and Germany. In addition to petrol-lead, two more sources of anthropogenic lead can be detected in sampled aerosols: the first one has low concentrations of lead (˜4 ng/m 3) and 206Pb /207Pb ˜ 1.157 , and is most likely lead, emitted in Turkey, that traveled across the eastern Mediterranean basin; the second type of aerosols contains a mixture of lead emitted in several countries including Turkey, Greece, and Ukraine ( 206Pb /207Pb value of 1.155-1.160; [Pb] ˜ 20-30 ng/m 3). Anthropogenic lead is more accessible for acid leaching than natural lead, therefore, it is more labile in the soil. The isotopic composition of lead in the acid-leached fraction of near-road soil profiles record the histor of alkyl-lead emission in the country. Based on changes in the isotopic composition of lead with soil depth, it is estimated that anthropogenic lead migrates into the soil at approximately 0.5 cm/y. A soil profile from a relatively remote area is less contaminated by anthropogenic lead and displays a different distribution of lead isotopic values with depth. The isotopic composition of lead suggests that natural lead in soils developed on carbonate bedrock is derived from clays, either from the rock-esidue (the clay fraction in the carbonate bedrock), or from airborne clay, but not from lead released from the carbonate fraction in the rock.

  18. Linking cases of illegal shootings of the endangered California condor using stable lead isotope analysis

    Energy Technology Data Exchange (ETDEWEB)

    Finkelstein, Myra E., E-mail: myraf@ucsc.edu [Microbiology and Environmental Toxicology Department, University of California, Santa Cruz, CA 95064 (United States); Kuspa, Zeka E. [Microbiology and Environmental Toxicology Department, University of California, Santa Cruz, CA 95064 (United States); Welch, Alacia [National Park Service, Pinnacles National Park, 5000 Highway 146, Paicines, CA 95043 (United States); Eng, Curtis; Clark, Michael [Los Angeles Zoo and Botanical Gardens, 5333 Zoo Drive, Los Angeles, CA 90027 (United States); Burnett, Joseph [Ventana Wildlife Society, 19045 Portola Dr. Ste. F-1, Salinas, CA 93908 (United States); Smith, Donald R. [Microbiology and Environmental Toxicology Department, University of California, Santa Cruz, CA 95064 (United States)

    2014-10-15

    Lead poisoning is preventing the recovery of the critically endangered California condor (Gymnogyps californianus) and lead isotope analyses have demonstrated that ingestion of spent lead ammunition is the principal source of lead poisoning in condors. Over an 8 month period in 2009, three lead-poisoned condors were independently presented with birdshot embedded in their tissues, evidencing they had been shot. No information connecting these illegal shooting events existed and the timing of the shooting(s) was unknown. Using lead concentration and stable lead isotope analyses of feathers, blood, and recovered birdshot, we observed that: i) lead isotope ratios of embedded shot from all three birds were measurably indistinguishable from each other, suggesting a common source; ii) lead exposure histories re-constructed from feather analysis suggested that the shooting(s) occurred within the same timeframe; and iii) two of the three condors were lead poisoned from a lead source isotopically indistinguishable from the embedded birdshot, implicating ingestion of this type of birdshot as the source of poisoning. One of the condors was subsequently lead poisoned the following year from ingestion of a lead buckshot (blood lead 556 µg/dL), illustrating that ingested shot possess a substantially greater lead poisoning risk compared to embedded shot retained in tissue (blood lead ∼20 µg/dL). To our knowledge, this is the first study to use lead isotopes as a tool to retrospectively link wildlife shooting events. - Highlights: • We conducted a case-based analysis of illegal shootings of California condors. • Blood and feather Pb isotopes were used to reconstruct the illegal shooting events. • Embedded birdshot from the three condors had the same Pb isotope ratios. • Feather and blood Pb isotopes indicated that the condors were shot in a common event. • Ingested shot causes substantially greater lead exposure compared to embedded shot.

  19. Lead (Pb) Isotope Baselines for Studies of Ancient Human Migration and Trade in the Maya Region

    National Research Council Canada - National Science Library

    Sharpe, Ashley E; Kamenov, George D; Gilli, Adrian; Hodell, David A; Emery, Kitty F; Brenner, Mark; Krigbaum, John

    2016-01-01

    .... We analyzed 60 rock samples for lead isotope ratios and a representative subset of samples for lead, uranium, and thorium concentrations across the Maya region, including the Northern Lowlands...

  20. A lead isotopic study of the human bioaccessibility of lead in urban soils from Glasgow, Scotland

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, John G., E-mail: J.G.Farmer@ed.ac.uk [School of GeoSciences, University of Edinburgh, Edinburgh, EH9 3JN, Scotland (United Kingdom); Broadway, Andrew [School of GeoSciences, University of Edinburgh, Edinburgh, EH9 3JN, Scotland (United Kingdom); Cave, Mark R.; Wragg, Joanna [British Geological Survey, Keyworth, Nottingham NG12 5GG, England (United Kingdom); Fordyce, Fiona M. [British Geological Survey, Edinburgh, EH9 3LA, Scotland (United Kingdom); Graham, Margaret C.; Ngwenya, Bryne T. [School of GeoSciences, University of Edinburgh, Edinburgh, EH9 3JN, Scotland (United Kingdom); Bewley, Richard J.F. [URS Corporation Ltd, Manchester, M1 6HS, England (United Kingdom)

    2011-11-01

    The human bioaccessibility of lead (Pb) in Pb-contaminated soils from the Glasgow area was determined by the Unified Bioaccessibility Research Group of Europe (BARGE) Method (UBM), an in vitro physiologically based extraction scheme that mimics the chemical environment of the human gastrointestinal system and contains both stomach and intestine compartments. For 27 soils ranging in total Pb concentration from 126 to 2160 mg kg{sup -1} (median 539 mg kg{sup -1}), bioaccessibility as determined by the 'stomach' simulation (pH {approx} 1.5) was 46-1580 mg kg{sup -1}, equivalent to 23-77% (mean 52%) of soil total Pb concentration. The corresponding bioaccessibility data for the 'stomach + intestine' simulation (pH {approx} 6.3) were 6-623 mg kg{sup -1} and 2-42% (mean 22%) of soil Pb concentration. The soil {sup 206}Pb/{sup 207}Pb ratios ranged from 1.057 to 1.175. Three-isotope plots of {sup 208}Pb/{sup 206}Pb against {sup 206}Pb/{sup 207}Pb demonstrated that {sup 206}Pb/{sup 207}Pb ratios were intermediate between values for source end-member extremes of imported Australian Pb ore (1.04) - used in the manufacture of alkyl Pb compounds (1.06-1.10) formerly added to petrol - and indigenous Pb ores/coal (1.17-1.19). The {sup 206}Pb/{sup 207}Pb ratios of the UBM 'stomach' extracts were similar (< 0.01 difference) to those of the soil for 26 of the 27 samples (r = 0.993, p < 0.001) and lower in 24 of them. A slight preference for lower {sup 206}Pb/{sup 207}Pb ratio was discernible in the UBM. However, the source of Pb appeared to be less important in determining the extent of UBM-bioaccessible Pb than the overall soil total Pb concentration and the soil phases with which the Pb was associated. The significant phases identified in a subset of samples were carbonates, manganese oxides, iron-aluminium oxyhydroxides and clays. - Highlights: {yields} We determined the human bioaccessibility of Pb in urban soils by in vitro extraction. {yields} We

  1. The lead isotopic age of the Earth can be explained by core formation alone.

    Science.gov (United States)

    Wood, Bernard J; Halliday, Alex N

    2010-06-10

    The meaning of the age of the Earth defined by lead isotopes has long been unclear. Recently it has been proposed that the age of the Earth deduced from lead isotopes reflects volatile loss to space at the time of the Moon-forming giant impact rather than partitioning into metallic liquids during protracted core formation. Here we show that lead partitioning into liquid iron depends strongly on carbon content and that, given a content of approximately 0.2% carbon, experimental and isotopic data both provide evidence of strong partitioning of lead into the core throughout the Earth's accretion. Earlier conclusions that lead is weakly partitioned into iron arose from the use of carbon-saturated (about 5% C) iron alloys. The lead isotopic age of the Earth is therefore consistent with partitioning into the core and with no significant late losses of moderately volatile elements to space during the giant impact.

  2. Speleothem isotopic evidence for rapid human-induced expansion of grasslands in Madagascar at 890 CE

    Science.gov (United States)

    Burns, S. J.; Godfrey, L.; Faina, P.; McGee, D.; Hardt, B. F.; Ranivoharimanana, L.; Randrianasy, J.

    2015-12-01

    The degree to which human activity impacted the landscape, vegetation and fauna of Madagascar remains under debate. Since the early 1920's, the prevailing hypothesis has been that the savannah grasslands that now cover 70% of Madagascar were the result of deforestation, which has also been tied to the disappearance of much of the island's endemic megafauna. Other studies suggest that Madagascar's grasslands are largely natural and that megafaunal extinctions may be climatically induced, leading some authors to question the entire narrative of extensive alteration of the landscape by early human activity. We collected two stalagmites, M14-AB2 and M14-AB3, from Anjohibe Cave in northwestern Madagascar (15.55°S, 46.89°E, 100 masl). Age models were constructed using 8 U/Th age determinations from AB2 and 10 from AB3. The samples began to grow at ~500 CE and were active at the time of collection. Carbon and oxygen stable isotope ratios were measured on 266 samples from AB2 and 173 samples from AB3, yielding sub-decadal temporal resolution. A rapid, more than 10 per mil increase in stalagmite carbon stable isotope ratios documents an almost complete transformation of the landscape from one with a flora dominated by C3 plants to a C4 grassland system. This transformation, well replicated in both stalagmites, occurred at approximately 890 +/- 20 CE and was complete in 100 years. Further, relatively constant oxygen isotope ratios across the carbon isotope transition demonstrate that landscape alteration was not related to changes in climate. We hypothesize that the transformation was caused primarily by expansion of the use of fire by early inhabitants of Madagascar to promote agriculture and the growth of grass as fodder for cattle. The resulting loss of forest habitat very likely increased environmental pressures on Madagascar's megafauna and accelerated their disappearance.

  3. Origin of the mysterious Yin-Shang bronzes in China indicated by lead isotopes

    Science.gov (United States)

    Sun, Wei-dong; Zhang, Li-peng; Guo, Jia; Li, Cong-ying; Jiang, Yu-hang; Zartman, Robert E.; Zhang, Zhao-feng

    2016-01-01

    Fine Yin-Shang bronzes containing lead with puzzlingly highly radiogenic isotopic compositions appeared suddenly in the alluvial plain of the Yellow River around 1400 BC. The Tongkuangyu copper deposit in central China is known to have lead isotopic compositions even more radiogenic and scattered than those of the Yin-Shang bronzes. Most of the Yin-Shang bronzes are tin-copper alloys with high lead contents. The low lead and tin concentrations, together with the less radiogenic lead isotopes of bronzes in an ancient smelting site nearby, however, exclude Tongkuangyu as the sole supplier of the Yin-Shang bronzes. Interestingly, tin ingots/prills and bronzes found in Africa also have highly radiogenic lead isotopes, but it remains mysterious as to how such African bronzes may have been transported to China. Nevertheless, these African bronzes are the only bronzes outside China so far reported that have lead isotopes similar to those of the Yin-Shang bronzes. All these radiogenic lead isotopes plot along ~2.0–2.5 Ga isochron lines, implying that deposits around Archean cratons are the most likely candidates for the sources. African cratons along the Nile and even micro-cratons in the Sahara desert may have similar lead signatures. These places were probably accessible by ancient civilizations, and thus are the most favorable suppliers of the bronzes. PMID:26988425

  4. A lead isotopic assessment of tree bark as a biomonitor of contemporary atmospheric lead

    Energy Technology Data Exchange (ETDEWEB)

    Patrick, Gavin J. [School of GeoSciences, University of Edinburgh, West Mains Road, Edinburgh EH9 3JN, Scotland (United Kingdom); Farmer, John G. [School of GeoSciences, University of Edinburgh, West Mains Road, Edinburgh EH9 3JN, Scotland (United Kingdom)], E-mail: J.G.Farmer@ed.ac.uk

    2007-12-15

    The outermost bark layer of trees, predominantly Scots pine (Pinus sylvestris), was sampled at 82 non-urban locations from six arbitrarily designated areas (Northwest, Northeast, Central Highlands, Central and East, Central and Southwest, Southeast), throughout Scotland during 2002-2003 and analysed for lead concentration and stable lead isotopes by flame atomic absorption spectrometry (AAS) and inductively coupled plasma-mass spectrometry (ICP-MS), respectively. The mean lead concentration and mean {sup 206}Pb/{sup 207}Pb ratio ({+-} 1 standard deviation, SD) for bark samples from the areas were as follows: Northwest (8.0 mg kg{sup -1}, 1.121 {+-} 0.014, n = 17), Northeast (8.9 mg kg{sup -1}, 1.117 {+-} 0.012, n = 12), Central Highlands (11.3 mg kg{sup -1}, 1.130 {+-} 0.010, n = 11), Central and East (35.3 mg kg{sup -1}, 1.120 {+-} 0.007, n = 10), Central and Southwest (20.6 mg kg{sup -1}, 1.125 {+-} 0.018, n = 22) and Southeast (34.4 mg kg{sup -1}, 1.120 {+-} 0.005, n = 10), with an overall mean lead concentration of 18.5 mg kg{sup -1} (range 0.6-146 mg kg{sup -1}, median 8.4 mg kg{sup -1}) and an overall mean {sup 206}Pb/{sup 207}Pb ratio of 1.122 {+-} 0.014 (range 1.089-1.168, median 1.122). The overall mean {sup 206}Pb/{sup 207}Pb ratio for bark was therefore significantly lower (p < 0.01, t test) than the mean atmospheric {sup 206}Pb/{sup 207}Pb ratio of 1.154 {+-} 0.006 (range 1.144-1.167, n = 50) and 1.154 {+-} 0.010 (range 1.134-1.171, n = 26) as determined in rainwater collected routinely at Glensaugh, Central Highlands, during 2002 and 2003, respectively. The bark {sup 206}Pb/{sup 207}Pb values, 90% of which lay between 1.10 and 1.14, were more akin to those recorded for the atmosphere (via rainwater, atmospheric particulates, moss, etc.) at various locations throughout Scotland during the 1990s, a decade over which the use of leaded petrol (mean {sup 206}Pb/{sup 207}Pb ratio = 1.076 {+-} 0.011) declined markedly before its complete withdrawal in 2000

  5. Simple, rapid method for the preparation of isotopically labeled formaldehyde

    Energy Technology Data Exchange (ETDEWEB)

    Hooker, Jacob Matthew [Port Jefferson, NY; Schonberger, Matthias [Mains, DE; Schieferstein, Hanno [Aabergen, DE; Fowler, Joanna S [Bellport, NY

    2011-10-04

    Isotopically labeled formaldehyde (*C.sup..sctn.H.sub.2O) is prepared from labeled methyl iodide (*C.sup..sctn.H.sub.3I) by reaction with an oxygen nucleophile having a pendant leaving group. The mild and efficient reaction conditions result in good yields of *C.sup..sctn.H.sub.2O with little or no *C isotopic dilution. The simple, efficient production of .sup.11CH.sub.2O is described. The use of the .sup.11CH.sub.2O for the formation of positron emission tomography tracer compounds is described. The reaction can be incorporated into automated equipment available to radiochemistry laboratories. The isotopically labeled formaldehyde can be used in a variety of reactions to provide radiotracer compounds for imaging studies as well as for scintillation counting and autoradiography.

  6. Differentiating sources of dissolved lead in mine waters using lead isotope techniques, Sullivan Mine, British Columbia

    Science.gov (United States)

    Lepitre, M. E.; Allen, D. M.; Mortensen, J. K.; Gabites, J. E.

    2003-01-01

    This study investigates the use of Pb isotopes in acid rock drainage studies and outlines a protocol for sampling and analysis of dissolved Pb in mine waters. Groundwaters and surface waters were sampled at the Sullivan Mine, British Columbia, to quantify Pb isotope ratios and to identify possible sources of Pb in mine effluent and back groundwaters, respectively. The Sullivan Deposit is a sediment-hosted Fe-Pb-Zn massive sulphide deposit with a well-defined homogeneous Pb isotopic composition, which provided a suitable end-member for the isotopic study. The Pb isotopic compositions of water samples define a mixing line between the homogeneous Pb isotopic signature of the Sullivan Ore and at least one other more radiogenic end-member. This end-member may correspond to Pb in the host rocks (Aldridge Formation), Pb from aerosols that have infiltrated the local surficial deposits with recharge, or Pb from the surficial deposits themselves. Further study is needed to more completely characterize the composition of potential isotopic end-members in the study area. The study demonstrates that different source regions for Pb have distinct and measurable isotopic compositions, which enable "fingerprinting" sources of Pb contamination that result from ore deposits or from other sources.

  7. Assessment of pollution aerosols sources above the Straits of Dover using lead isotope geochemistry.

    Science.gov (United States)

    Deboudt, K; Flament, P; Weis, D; Mennessier, J P; Maquinghen, P

    1999-09-15

    We assess the capability of lead isotopes to study the transport of pollution aerosols above the Straits of Dover by collecting atmospheric aerosols above the Eastern Channel and the Southern Bight of the North Sea. During the same period, we characterized the lead isotopic signature of the main industrial sources on the French coast near the Straits of Dover. Urban and automobile-derived aerosols were also collected. Due to the phasing out of lead in gasoline, the urban isotopic composition (206Pb/207Pb = 1.158 +/- 0.003) has become more radiogenic, although it is highly variable. On a regional scale, major industrial emissions have a well-defined isotopic composition (1.13 isotopic compositions, it can be shown that lead aerosols originating from eastern Europe have an isotopic signature (1.145 isotopic composition of west-European lead aerosols (1.111 < 206Pb/207Pb < 1.142). The influence of remote North American sources is suggested, with caution, due to uncertainties in meteorological calculations.

  8. Lead isotopic evidence for selective uptake of radium in illite

    Energy Technology Data Exchange (ETDEWEB)

    Hidaka, H.; Horie, K. [Department of Earth and Planetary Systems Science, Hiroshima University Higashi-Hiroshima 739-8526 (Japan); Gauthier-Lafaye, F. [Centre de Geochimie de la Surface, UMR7517-CNRS-ULP, 67084 Strasbourg (France)

    2005-07-01

    Full text of publication follows: Radium has no stable isotopes. {sup 226}Ra having the longest half-life (T{sub 1/2} = 1600 year) among radium radioisotopes exists as a precursor of decay product from {sup 238}U in nature, and finally decays to the stable isotope {sup 206}Pb. Long-lived nuclides such as {sup 226}Ra may be profoundly fractionated from their parents in association with intense geochemical events in the terrestrial environments. Enrichment of Ra resulted from vegetation cycle and selective uptake into clay minerals has been reported [1,2]. It is of particular interest to understand the geochemical behaviors of Ra from the viewpoint of long-termed repository safety of radio-nuclear waste. We report here geochemical evidence of selective uptake of Ra ({sup 226}Ra) into clay minerals studied from the Pb isotopic compositions. The sample from sandstone layer at underground drift close to natural reactor zone 13 at the Oklo uranium deposits, Gabon. Several tiny illite grains sized about 100 {mu}m were found in fine calcite veins with 0.1 to 2 mm width in quartz matrix texture. Isotopic analyses of Pb and some related elements (U, Rb, Sr, Cs and Ba) in individual minerals were carried out by a Sensitive High Resolution Ion Microprobe (SHRIMP) at Hiroshima University. The Pb isotopic data of quartz and calcite in the sample provide the geochronological information corresponding to the formation of 2.15 billion year-old basement rocks and the occurrence of later hydrothermal activity in this region at 0.88 billion years, respectively. On the other hand, illite shows high enrichment of {sup 206}Pb, which cannot be explained simply from normal U decays. {sup 206}Po-enriched illite grains also show a strong enrichment of Ba. Such an enrichment of Ba is not observed in the neighboring minerals of illite grains. Considering that Ba has been used as a chemical tracer of {sup 226}Ra because of the chemical similarities between Ba and Ra, our result strongly

  9. Lead Contamination in Cocoa and Cocoa Products: Isotopic Evidence of Global Contamination

    National Research Council Canada - National Science Library

    Charley W. Rankin; Jerome O. Nriagu; Jugdeep K. Aggarwal; Toyin A. Arowolo; Kola Adebayo; A. Russell Flegal

    2005-01-01

    In this article we present lead concentrations and isotopic compositions from analyses of cocoa beans, their shells, and soils from six Nigerian cocoa farms, and analyses of manufactured cocoa and chocolate products...

  10. Lead isotopes and the origin of granulite and eclogite inclusions in deep-seated pipes

    Science.gov (United States)

    Lovering, J.F.; Tatsumoto, M.

    1968-01-01

    The isotopic composition of lead and the concentrations of lead, uranium, and thorium in Delegate basic pipes from Australia and in South African kimberlite pipes have been determined. The observed 238U/204Pb and observed 232Th/238U of eclogite inclusions in the pipes range from 2.9 to 18.7 and from 3.5 to 5.9, respectively. This result as well as the isotopic composition of lead suggests that the upper mantle is chemically heterogeneous with regard to the trace elements. Pyrochemically extracted leads from eclogite inclusions in the Delegate basic pipes and in a South African kimberlite pipe appear to be different in isotopic compositions from leads extracted from the host rock (matrix). These data are consistent with the hypothesis that the eclogitic inclusions in deep-seated pipes are of "accidental" origin and represent upper mantle materials caught up in the host materials during their intrusion. Lead extracted from a two-pyroxene granulite inclusion in one of the Delegate pipes has an isotopic composition indistinguishable from lead in the host rock. This observation is consistent either with a "cognate" origin for the granulite inclusion or with a modified "accidental" origin in which the isotopic composition of the original lead in the inclusion has been contaminated by lead from the host magma. Other evidence would indicate that an "accidental" origin be preferred. ?? 1968.

  11. Application of lead and strontium isotope ratio measurements for the origin assessment of uranium ore concentrates.

    Science.gov (United States)

    Varga, Zsolt; Wallenius, Maria; Mayer, Klaus; Keegan, Elizabeth; Millet, Sylvain

    2009-10-15

    Lead and strontium isotope ratios were used for the origin assessment of uranium ore concentrates (yellow cakes) for nuclear forensic purposes. A simple and low-background sample preparation method was developed for the simultaneous separation of the analytes followed by the measurement of the isotope ratios by multicollector inductively coupled plasma mass spectrometry (MC-ICPMS). The lead isotopic composition of the ore concentrates suggests applicability for the verification of the source of the nuclear material and by the use of the radiogenic (207)Pb/(206)Pb ratio the age of the raw ore material can be calculated. However, during data interpretation, the relatively high variation of the lead isotopic composition within the mine site and the generally high contribution of natural lead as technological contamination have to be carefully taken into account. The (87)Sr/(86)Sr isotope ratio is less prone to the variation within one mine site and less affected by the production process, thus it was found to be a more purposeful indicator for the origin assessment and source verification than the lead. The lead and strontium isotope ratios measured and the methodology developed provide information on the initial raw uranium ore used, and thus they can be used for source attribution of the uranium ore concentrates.

  12. Lead isotopic evolution of Archean continental crust, Northern Tanzania

    Science.gov (United States)

    Bellucci, J. J.; McDonough, W. F.; Rudnick, R. L.; Walker, R. J.

    2010-12-01

    The continental crust is stratified in composition; the upper crust is generally enriched in highly incompatible trace elements relative to the lower crust [1]. The Western Granulite section of the Mozambique Belt of Northern Tanzania yields Archean Nd model ages and has zircons with U-Pb ages of ~2.6 Ga [2,3], but was strongly re-worked during the Pan-African Orogeny, ca. 560 Ma [2,3,4]. Here we use time-integrated Pb isotopic modeling for lower and middle crustal xenoliths, as well as upper crustal granulites to determine the timing of, and degree of intra-crustal differentiation. The Pb isotopic compositions of most feldspars in the lower crustal samples, measured via LA-MC-ICPMS, fall on the trend defined by the Tanzanian Craton [5] and therefore, were most likely extracted from the mantle at a similar time, ca. 2.7 Ga. However, some xenoliths fall off this trend and show enrichment in 207Pb/204Pb, which we interpret as reflecting derivation from more heterogeneous mantle than that sampled in the Tanzanian Craton. In contrast to lower crustal xenoliths from the Tanzanian Craton [5], we see no single feldspar Pb-Pb isochrons, which indicates complete re-homogenization of the Pb isotopic composition of the feldspars in the lower crust of the Mozambique Belt during the Pan-African Orogeny, and heating to > 600°C [5]. Using time integrated Pb modeling, the upper crust of the Western Granulites is enriched in U by ˜ 2.5 relative to that of the lower crust, which must have taken place around the time of mantle extraction (ca. 2.7 Ga). In addition, these calculations are consistent with a Th/U ratio of ˜ 4 for the bulk lower crust and ˜ 3 for the bulk upper crust. The common Pb isotopic composition of a single middle crustal xenolith implies a Th/U of 20, but is unlikely to be generally representative of the middle crust. [1] Rudnick, R. L. and Gao, S. (2003). In the Crust, vol. 3, Treatise on Geochemistry:1-64. [2] Mansur, A. (2008) Masters Thesis, University of

  13. Lead (Pb) Isotope Baselines for Studies of Ancient Human Migration and Trade in the Maya Region.

    Science.gov (United States)

    Sharpe, Ashley E; Kamenov, George D; Gilli, Adrian; Hodell, David A; Emery, Kitty F; Brenner, Mark; Krigbaum, John

    2016-01-01

    We examined the potential use of lead (Pb) isotopes to source archaeological materials from the Maya region of Mesoamerica. The main objectives were to determine if: 1) geologic terrains throughout the Maya area exhibit distinct lead isotope ratios (206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb), and 2) a combination of lead and strontium ratios can enhance sourcing procedures in the Mesoamerica region. We analyzed 60 rock samples for lead isotope ratios and a representative subset of samples for lead, uranium, and thorium concentrations across the Maya region, including the Northern Lowlands of the Mexican Yucatan Peninsula, the Southern Lowlands of Guatemala and Belize, the Volcanic Highlands, the Belizean Maya Mountains, and the Metamorphic Province/Motagua Valley. Although there is some overlap within certain sub-regions, particularly the geologically diverse Metamorphic Province, lead isotopes can be used to distinguish between the Northern Lowlands, the Southern Lowlands, and the Volcanic Highlands. The distinct lead isotope ratios in the sub-regions are related to the geology of the Maya area, exhibiting a general trend in the lowlands of geologically younger rocks in the north to older rocks in the south, and Cenozoic volcanic rocks in the southern highlands. Combined with other sourcing techniques such as strontium (87Sr/86Sr) and oxygen (δ18O), a regional baseline for lead isotope ratios can contribute to the development of lead isoscapes in the Maya area, and may help to distinguish among geographic sub-regions at a finer scale than has been previously possible. These isotope baselines will provide archaeologists with an additional tool to track the origin and movement of ancient humans and artifacts across this important region.

  14. Stable lead isotopes in environmental health with emphasis on human investigations

    Energy Technology Data Exchange (ETDEWEB)

    Gulson, Brian [Graduate School of the Environment, Macquarie University, Sydney NSW 2109 (Australia); CSIRO Exploration and Mining North Ryde NSW 1670 (Australia)], E-mail: bgulson@gse.mq.edu.au

    2008-08-01

    There has been widespread use of stable lead isotopes in the earth sciences for more than 40 years focussed on the origin and age of rocks and minerals with lesser application in environmental investigations where the emphasis has been directed typically to the source of lead in environmental media such as air, water and soils. In contrast, the number of environmental health investigations focussed on humans (and primates) is limited in spite of the demonstrated utility of the approach in pioneering studies in the early 1970's. This paper reviews the status of lead isotopes in human investigations especially over the past 2 decades, the period over which most activity has taken place. Following a brief introduction to the method, examples are provided illustrating the use of lead isotopes in a wide spectrum of activities including sources and pathways of lead in diverse environments from urban to mining communities, various applications associated with pregnancy, the contribution of bone lead to blood lead including in the elderly, the half-life of lead in blood, and lead in bones and other media. A brief outline of critical research on non-human primates is also given. The lead isotope method is a powerful technique for tracing lead and could be employed more widely in human investigations.

  15. Origins of inhabitants from the 16th century Sala (Sweden) silver mine cemetery – a lead isotope perspective

    DEFF Research Database (Denmark)

    Price, T. Douglas; Frei, Robert; Bäckström, Ylva

    2017-01-01

    however. Here we utilize lead isotopes as an additional isotopic tracer to identify origins. The lead isotope investigations pinpoint several areas outside of the Sala region where some of the inhabitants originated. In addition, the study documents the benefits of using lead isotopes in human...... these grave types, as well as harsh conditions of life. Strontium and oxygen isotopes have been used previously to investigate the place of origin of the cemetery inhabitants and clear differences among the types of graves were seen in the isotope results. Place of origin was more difficult to ascertain...

  16. Provenance of dust to Antarctica: A lead isotopic perspective

    Science.gov (United States)

    Gili, Stefania; Gaiero, Diego M.; Goldstein, Steven L.; Chemale, Farid, Jr.; Koester, Edinei; Jweda, Jason; Vallelonga, Paul; Kaplan, Michael R.

    2016-03-01

    Antarctic ice preserves an ~800 kyr record of dust activity in the Southern Hemisphere. Major efforts have been dedicated to elucidate the origin of this material in order to gain greater insight into the atmospheric dust cycle. On the basis of Pb isotopes in Antarctic dust samples and potential sources, this contribution demonstrates for the first time that Patagonia is the main contributor of dust to Antarctica during interglacial periods as well as glacials, although the potential importance of Tierra del Fuego remains unclear because of its geochemical similarities to Patagonia. An important new finding is that the Puna-Altiplano sector of the continent is a second important dust source to eastern Antarctica during both glacials and interglacials, being more prominent during interglacials. The data indicate South America is the primary dust source to Antarctica during both glacials and interglacials.

  17. Regional variations in the lead isotopic composition of galena from southern Korea with implications for the discrimination of lead provenance

    Science.gov (United States)

    Jeong, Youn-Joong; Cheong, Chang-sik; Shin, Dongbok; Lee, Kwang-Sik; Jo, Hui Je; Gautam, Mukesh Kumar; Lee, Insung

    2012-11-01

    This study presents a comprehensive database (n = 215) of lead isotopes in galena from the southern Korean peninsula using new and published data. Of the 69 metal mines examined, predominantly skarn- and hydrothermal-type Pb-Zn-Au-Ag-Cu deposits were observed and were associated with Mesozoic magmatic activities. Galena samples from each geotectonic unit showed discrete lead isotopic signatures. The Gyeongsang basin samples were characteristically unradiogenic and had restricted variations in lead isotopic composition (206Pb/204Pb = 18.16-18.59, 207Pb/204Pb = 15.48-15.64, 208Pb/204Pb = 37.87-38.77). Their 208Pb/204Pb range indicated an involvement of source materials less thorogenic than the associated granites. The galena samples from Cambro-Ordovician carbonate rocks of the northeastern Yeongnam massif and eastern Taebaeksan basin had the most radiogenic 206Pb/204Pb (19.28 ± 0.14) and 207Pb/204Pb (15.833 ± 0.027) ratios. Their lead isotopic trend indicated a combined contribution of ore lead from granitic magmas, Precambrian basements, and overlain host rocks. Less radiogenic galena samples from the middle to southwestern parts of the Yeongnam massif and Okcheon belt showed limited lead isotopic variations (206Pb/204Pb = 18.332 ± 0.065, 207Pb/204Pb = 15.693 ± 0.012, 208Pb/204Pb = 38.93 ± 0.07 on average), probably resulted from mixing with a common crustal basement. The differences in lead isotopes between the radiogenic and unradiogenic groups from the Yeongnam massif and Okcheon belt may reflect the spatial dissimilarity of involved crustal rocks. The old crust appears to have significantly contributed ore lead to galenas from the western Gyeonggi massif, but the geochronological meaning of their steep 207Pb/204Pb-206Pb/204Pb trend is not clear. The comprehensive database constructed by the present study suggests that lead province in the southern Korean peninsula may be subdivided into four discrete zones. Linear discriminant analysis showed that more

  18. Isotopic source signatures for atmospheric lead: the Southern Hemisphere

    Science.gov (United States)

    Bollhöfer, A.; Rosman, K. J. R.

    2000-10-01

    Aerosols collected between 1994 and 1999 at more than 70 different sites affecting the Southern Hemisphere have been measured for their 206Pb/ 207Pb, 208Pb/ 207Pb and 206Pb/ 204Pb ratios and Pb concentrations. Lower ratios are found at the southern tips of Africa, Australia and South America probably due to the supply of alkyllead from a common supplier such as Associated Octel. The ratios increase in a northerly direction probably due to a changing market share in alkyllead or an increasing industrial Pb contribution. The geographical variations in isotopic signatures made it possible to broadly characterize the different regions that influence the Southern Hemisphere. Brazil and Argentina exhibited 206Pb/ 207Pb, 208Pb/ 207Pb and 206Pb/ 204Pb ratios in aerosols of 1.141-1.184, 2.416-2.442 and 17.77-18.57, respectively. Mexican aerosols had values of 1.188-1.197, 2.452-2.463 and 18.46-18.73. Aerosols sampled in Chile had low ratios in the South of 1.063-1.094, 2.337-2.373 and 16.46-17.13 which increased in a northerly direction. Emissions from South Africa were characterized by ratios 1.067-1.090, 2.340-2.358 and 16.53-16.99. In 1994-1995 Australia and New Zealand had ratios of 1.060-1.193, 2.324-2.445 and 16.08-18.54. In 1997 however, the range was narrower: 1.072-1.112, 2.342-2.398 and 16.55-17.36, respectively. These isotopic signatures are potentially useful for tracing sources of pollution and the movement of air-masses on a global scale.

  19. Rapidly assessing changes in bone mineral balance using natural stable calcium isotopes

    Science.gov (United States)

    Morgan, Jennifer L. L.; Skulan, Joseph L.; Gordon, Gwyneth W.; Romaniello, Stephen J.; Smith, Scott M.; Anbar, Ariel D.

    2012-06-01

    The ability to rapidly detect changes in bone mineral balance (BMB) would be of great value in the early diagnosis and evaluation of therapies for metabolic bone diseases such as osteoporosis and some cancers. However, measurements of BMB are hampered by difficulties with using biochemical markers to quantify the relative rates of bone resorption and formation and the need to wait months to years for altered BMB to produce changes in bone mineral density large enough to resolve by X-ray densitometry. We show here that, in humans, the natural abundances of Ca isotopes in urine change rapidly in response to changes in BMB. In a bed rest experiment, use of high-precision isotope ratio MS allowed the onset of bone loss to be detected in Ca isotope data after about 1 wk, long before bone mineral density has changed enough to be detectable with densitometry. The physiological basis of the relationship between Ca isotopes and BMB is sufficiently understood to allow quantitative translation of changes in Ca isotope abundances to changes in bone mineral density using a simple model. The rate of change of bone mineral density inferred from Ca isotopes is consistent with the rate observed by densitometry in long-term bed rest studies. Ca isotopic analysis provides a powerful way to monitor bone loss, potentially making it possible to diagnose metabolic bone disease and track the impact of treatments more effectively than is currently possible.

  20. Lead isotope determinations from sulfide mineral occurrences--Russian Far East

    Science.gov (United States)

    Church, Stanley E.; Goryachev, Nikolai A.; Shpikerman, Vladimir I.

    2013-01-01

    The lead isotope database for sulfide deposits and occurrences in the Russian Far East was funded by the Mineral Resources Program, U.S. Geological Survey (USGS) in conjunction with the collaborative studies of mineral resources by the Russian Academy of Sciences and the U. S. Geological Survey (Nokleberg and others, 1996). Comparisons of these data with similar lead isotope data from Alaska published in Church, Delevaux, and others (1987) and Gaccetta and Church (1989) provide a basis for the following three-fold project objectives: 1. To utilize lead isotope signatures, in conjunction with regional mapping, to assess the relative ages and to categorize the types of mineral deposits studied, 2. To relate the lead isotope and trace-element geochemical signatures of specific deposits and occurrences to ore-forming processes, and 3. To use the lead isotope data to correlate lithotectonic terranes within the northern Cordillera (Alaska, Yukon Territories and British Columbia in Canada, and the western Cordillera of the United States). The report by Church, Gray, and others (1987) shows how this fingerprinting methodology can be applied to trace the offset of lithotectonic (or lithostratigraphic as labeled by some authors) terranes.The lead isotope data presented in table 1 represent the work completed on sulfide mineral deposits located in the Russian Far East from 1993 to 1995, when this study was terminated due to lack of funding. The lead isotope data are reported here for use by investigators who may find them of value in mineral exploration. No attempt is made to summarize the voluminous literature on these mineral deposits.

  1. Asian industrial lead inputs to the North Pacific evidenced by lead concentrations and isotopic compositions in surface waters and aerosols.

    Science.gov (United States)

    Gallon, Céline; Ranville, Mara A; Conaway, Christopher H; Landing, William M; Buck, Clifton S; Morton, Peter L; Flegal, A Russell

    2011-12-01

    Recent trends of atmospheric lead deposition to the North Pacific were investigated with analyses of lead in aerosols and surface waters collected on the fourth Intergovernmental Oceanographic Commission Contaminant Baseline Survey from May to June, 2002. Lead concentrations of the aerosols varied by 2 orders of magnitude (0.1-26.4 pmol/m(3)) due in part to variations in dust deposition during the cruise. The ranges in lead aerosol enrichment factors relative to iron (1-119) and aluminum (3-168) were similar, evidencing the transport of Asian industrial lead aerosols across the North Pacific. The oceanic deposition of some of those aerosols was substantiated by the gradient of lead concentrations of North Pacific waters, which varied 3-fold (32.7-103.5 pmol/kg), were highest along with the Asian margin of the basin, and decreased eastward. The hypothesized predominance of Asian industrial lead inputs to the North Pacific was further corroborated by the lead isotopic composition of ocean surface waters ((206)Pb/(207)Pb = 1.157-1.169; (208)Pb/(206)Pb = 2.093-2.118), which fell within the range of isotopic ratios reported in Asian aerosols that are primarily attributed to Chinese industrial lead emissions.

  2. Rubidium isotopes in primitive chondrites: Constraints on Earth's volatile element depletion and lead isotope evolution

    Science.gov (United States)

    Nebel, O.; Mezger, K.; van Westrenen, W.

    2011-05-01

    The bulk silicate Earth (BSE) shows substantial deficits in volatile elements compared to CI-chondrites and solar abundances. These deficits could be caused by pre-accretionary depletion in the solar nebula during condensation of solids, or by later heat-driven evaporation during collision of small bodies that later accreted to form the Earth. The latter is considered to result in isotope fractionation for elements with low condensation temperatures that correlates with the degree of depletion. Here, we report first high-precision isotope ratio measurements of the moderately volatile and lithophile trace element Rb. Data from seventeen chondrite meteorites show that their Rb isotope abundances are nearly indistinguishable from Earth, not deviating more than 1 per mil in their 87Rb/85Rb. The almost uniform solar system Rb isotope pool suggests incomplete condensation or evaporation in a single stage is unlikely to be the cause of the volatile element deficit of the Earth. As Rb and Pb have similar condensation temperatures, we use their different degrees of depletion in the BSE to address the mechanisms and timing of terrestrial volatile depletion. The Rb isotope data are consistent with a scenario in which the volatile budget of the Earth was generated by a mixture of a highly volatile-element depleted early Proto-Earth with undepleted material in the course of terrestrial accretion. Observed Pb and Rb abundances and U-Pb and Rb-Sr isotope systematics suggest that volatile addition occurred at approximately the same time at which last core-mantle equilibration was achieved. In line with previous suggestions, this last equilibration involved a second stage of Pb (but not Rb) depletion from the BSE. The timing of this second Pb loss event can be constrained to ~ 110 Ma after the start of the solar system. This model supports a scenario with core storage of Pb in the aftermath of a putative Moon forming giant impact that also delivered the bulk of the volatile

  3. The Rosetta Stone of isotope science and the uranium/lead system.

    Science.gov (United States)

    De Laeter, John

    2011-01-01

    The nucleosynthetic characteristics of U and Pb, together with the interconnectivity between these elements by two radioactive decay chains, are the foundation on which the U/Pb system was able to make a unique contribution to isotope science. The Rosetta Stone is an ancient Egyptian tablet that enabled previously indecipherable hieroglyphics to be translated. In a similar manner, the isotopic investigation of the U/Pb system, by a variety of mass spectrometric instrumentation, has led to our knowledge of the age of the Earth and contributed to thermochronology. In a similar manner, climate change information has been garnered by utilizing the U-Disequilibrium Series to measure the ages of marine archives. The impact of Pb in the environment has been demonstrated in human health, particularly at the peak of leaded petrol consumption in motor vehicles in the 1970s. Variations in the isotopic composition of lead in samples enable the source of the lead to be "fingerprinted" so as to trace the history of the Pb in ice cores and aerosols. The discovery of nuclear fission of (235)U led to the development of nuclear reactors and the isotopic investigation of the Oklo natural reactors. The mass spectrometer is the modern Rosetta Stone of isotope science, which has enabled the isotopic hieroglyphics of the U/Pb system to be investigated to reveal new horizons in our understanding of nature, and to address a number of societal and environmental problems.

  4. Shergottite Lead Isotope Signature in Chassigny and the Nakhlites

    Science.gov (United States)

    Jones, J. H.; Simon, J. I.

    2017-01-01

    The nakhlites/chassignites and the shergottites represent two differing suites of basaltic martian meteorites. The shergottites have ages less than or equal to 0.6 Ga and a large range of initial Sr-/Sr-86 and epsilon (Nd-143) ratios. Conversely, the nakhlites and chassignites cluster at 1.3-1.4 Ga and have a limited range of initial Sr-87/Sr-86 and epsilon (Nd-143). More importantly, the shergottites have epsilon (W-182) less than 1, whereas the nakhlites and chassignites have epsilon (W-182) approximately 3. This latter observation precludes the extraction of both meteorite groups from a single source region. However, recent Pb isotopic analyses indicate that there may have been interaction between shergottite and nakhlite/chassignite Pb reservoirs.Pb Analyses of Chassigny: Two different studies haveinvestigated 207Pb/204Pb vs. 206Pb/204Pb in Chassigny: (i)TIMS bulk-rock analyses of successive leaches and theirresidue [3]; and (ii) SIMS analysis of individual minerals[4]. The bulk-rock analyses fall along a regression of SIMSplagioclase analyses that define an errorchron that is olderthan the Solar System (4.61±0.1 Ga); i.e., these define amixing line between Chassigny’s principal Pb isotopic components(Fig. 1). Augites and olivines in Chassingy (notshown) also fall along or near the plagioclase regression [4].This agreement indicates that the whole-rock leachateslikely measure indigenous, martian Pb, not terrestrial contamination[5]. SIMS analyses of K-spars and sulfides definea separate, sub-parallel trend having higher 207Pb/206Pbvalues ([4]; Fig. 1). The good agreement between the bulkrockanalyses and the SIMS analyses of plagioclases alsoindicates that the Pb in the K-spars and sulfides cannot be amajor component of Chassigny.The depleted reservoir sampled by Chassigny plagioclaseis not the same as the solar system initial (PAT) andrequires a multi-stage origin. Here we show a two-stagemodel (Fig. 1) with a 238U/204Pb (µ) of 0.5 for 4.5-2.4 Gaand a µ of

  5. Lead Isotopic Composition and Lead Source of the Huogeqi Cu-Pb-Zn Deposit, Inner Mongolia, China

    Institute of Scientific and Technical Information of China (English)

    ZHU Xiaoqing; ZHANG Qian; HE Yuliang; ZHU Chaohui

    2006-01-01

    The Huogeqi orefield located on the northern side of Mt. Langshan, Inner Mongolia occurs in the Middle Proterozoic Langshan Group metamorphic rocks, and the orebodies are stratiform. In the past twenty years, many Chinese geologists have conducted researches on the Huogeqi Cu-Pb-Zn deposit, but there has been still a controversy on its origin. Some advocate that the deposit is of sedimentary-metamorphic reworking origin, some hold that it is of sea-floor SEDEX origin, and others have a preference for magmatic superimposition origin. The crux of the controversy is that there is no common understanding about the source of ore-forming materials. In this paper, the Pb isotopic compositions of regional Achaean-Early Proterozoic basement rocks, various types of sedimentarymetamorphic rocks and volcanic rocks in the mining district, Late Proterozoic and Hercynian magmatic rocks are introduced and compared with the ore-lead composition, so as to constrain the source of the ore lead. The result indicates that (1) sulfides in the ores have homogeneous Pb isotopic compositions, showing a narrow variation range. Their 206Pb/204Pb ratios are within a range of 17.027-17.317; 207pb/204pb ratios, 15.451-15.786 and 208Pb/204pb ratios, 36.747-37.669; (2) the Pb isotopic compositions of the regional Achaean-Early Proterozoic basement rocks are characteristic of the old Pb isotopic composition at the early-stage evolution of the Earth, which varies over a wider range,reflecting significant differences in Pb isotopic compositions of the ores. All this indicates that the source of ore lead has no bearing on the basement rocks; (3) the sedimentary-metamorphic rocks in the mining district are characterized by highly variable and more radiogenic Pb isotopic compositions and their Pb isotopic ratios are obviously higher than those of ores, demonstrating that ore lead did not result from metamorphic reworking of these rocks; (4) Pb isotopic compositions of Late Proterozoic diorite-gabbro and

  6. Lead isotope studies of the Guerrero composite terrane, west-central Mexico: implications for ore genesis

    Science.gov (United States)

    Potra, Adriana; Macfarlane, Andrew W.

    2014-01-01

    New thermal ionization mass spectrometry and multi-collector inductively coupled plasma mass spectrometry Pb isotope analyses of three Cenozoic ores from the La Verde porphyry copper deposit located in the Zihuatanejo-Huetamo subterrane of the Guerrero composite terrane are presented and the metal sources are evaluated. Lead isotope ratios of 3 Cenozoic ores from the El Malacate and La Esmeralda porphyry copper deposits located in the Zihuatanejo-Huetamo subterrane and of 14 ores from the Zimapan and La Negra skarn deposits from the adjoining Sierra Madre terrane are also presented to look for systematic differences in the lead isotope trends and ore metal sources among the proposed exotic tectonostratigraphic terranes of southern Mexico. Comparison among the isotopic signatures of ores from the Sierra Madre terrane and distinct subterranes of the Guerrero terrane supports the idea that there is no direct correlation between the distinct suspect terranes of Mexico and the isotopic signatures of the associated Cenozoic ores. Rather, these Pb isotope patterns are interpreted to reflect increasing crustal contribution to mantle-derived magmas as the arc advanced eastward onto a progressively thicker continental crust. The lead isotope trend observed in Cenozoic ores is not recognized in the ores from Mesozoic volcanogenic massive sulfide and sedimentary exhalative deposits. The Mesozoic ores formed prior to the amalgamation of the Guerrero composite terrane to the continental margin, which took place during the Late Cretaceous, in intraoceanic island arc and intracontinental marginal basin settings, while the Tertiary deposits formed after this event in a continental arc setting. Lead isotope ratios of the Mesozoic and Cenozoic ores appear to reflect these differences in tectonic setting of ore formation. Most Pb isotope values of ores from the La Verde deposit (206Pb/204Pb = 18.674-18.719) are less radiogenic than those of the host igneous rocks, but plot within the

  7. Effectiveness of leaded petrol phase-out in Tianjin, China based on the aerosol lead concentration and isotope abundance ratio

    Energy Technology Data Exchange (ETDEWEB)

    Wang Wan [Chinese Research Academy of Environmental Sciences, Beijing 100012 (China); Liu Xiande [Chinese Research Academy of Environmental Sciences, Beijing 100012 (China)]. E-mail: liuxdlxd@hotmail.com; Zhao Liwei [Tianjin Environmental Monitoring Center, Tianjin, 300190 (China); Guo, Dongfa [Beijing Research Institute of Uranium Geology, Beijing 100029 (China); Tian Xiaodan [University of Antwerp, UA, B-2610 Wilrijk-Antwerpen (Belgium); Adams, Freddy [University of Antwerp, UA, B-2610 Wilrijk-Antwerpen (Belgium)

    2006-07-01

    The phase-out of leaded petrol has been a measure widely used to reduce atmospheric lead pollution. Since the 1980s, China began to promote unleaded petrol. In order to assess the effectiveness of the measure an isotope fingerprint technique was applied for aerosol samples in the city of Tianjin. After dilute acid leaching, the lead concentration and isotope abundance ratios were determined for 123 samples collected in Tianjin during eight years (1994-2001). The {sup 206}Pb / {sup 207}Pb ratio was lower in summer, when coal combustion emission was low and vehicle exhaust became more important, indicating that the {sup 206}Pb / {sup 207}Pb ratio of leaded petrol in Tianjin is lower than that of aerosol samples. The {sup 206}Pb / {sup 207}Pb ratio gradually increased from 1994 to 2001, a trend that suggests that the contribution from vehicle exhaust was diminishing. Overall, the measurements matched well with national statistical data of leaded and unleaded petrol production. After the nationwide switch to unleaded gasoline, comprehensive control measures are urgently needed to reduce air lead pollution in China, as aerosol lead reduced slightly but remains at a relatively high level.

  8. Effectiveness of leaded petrol phase-out in Tianjin, China based on the aerosol lead concentration and isotope abundance ratio

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Wan; Liu, Xiande [Chinese Research Academy of Environmental Sciences, Beijing 100012 (China); Zhao, Liwei [Tianjin Environmental Monitoring Center, Tianjin, 300190 (China); Guo, Dongfa [Beijing Research Institute of Uranium Geology, Beijing 100029 (China); Tian, Xiaodan; Adams, Freddy [University of Antwerp, UA, B-2610 Wilrijk-Antwerpen (Belgium)

    2006-07-01

    The phase-out of leaded petrol has been a measure widely used to reduce atmospheric lead pollution. Since the 1980s, China began to promote unleaded petrol. In order to assess the effectiveness of the measure an isotope fingerprint technique was applied for aerosol samples in the city of Tianjin. After dilute acid leaching, the lead concentration and isotope abundance ratios were determined for 123 samples collected in Tianjin during eight years (1994-2001). The {sup 206}Pb/{sup 207}Pb ratio was lower in summer, when coal combustion emission was low and vehicle exhaust became more important, indicating that the {sup 206}Pb/{sup 207}Pb ratio of leaded petrol in Tianjin is lower than that of aerosol samples. The {sup 206}Pb/{sup 207}Pb ratio gradually increased from 1994 to 2001, a trend that suggests that the contribution from vehicle exhaust was diminishing. Overall, the measurements matched well with national statistical data of leaded and unleaded petrol production. After the nationwide switch to unleaded gasoline, comprehensive control measures are urgently needed to reduce air lead pollution in China, as aerosol lead reduced slightly but remains at a relatively high level. (author)

  9. Identification of the sources of metal (lead) contamination in drinking waters in north-eastern Tasmania using lead isotopic compositions.

    Science.gov (United States)

    Harvey, P J; Handley, H K; Taylor, M P

    2015-08-01

    This study utilises a range of scientific approaches, including lead isotopic compositions, to differentiate unknown sources of ongoing lead contamination of a drinking water supply in north-eastern Tasmania, Australia. Drinking water lead concentrations are elevated above the Australian Drinking Water Guideline (10 μg/L), reaching 540 μg/L in the supply network. Water lead isotopic compositions from the town of Pioneer ((208)Pb/(207)Pb 2.406, (206)Pb/(207)Pb 1.144 to (208)Pb/(207)Pb 2.360, (206)Pb/(207)Pb 1.094) and Ringarooma ((208)Pb/(207)Pb 2.398, (206)Pb/(207)Pb 1.117) are markedly different from the local bedrock ((208)Pb/(207)Pb 2.496, (206)Pb/(207)Pb 1.237). The data show that the lead in the local waters is sourced from a combination of dilapidated drinking water infrastructure, including lead jointed pipelines, end-of-life polyvinyl chloride pipes and household plumbing. Drinking water is being inadvertently contaminated by aging infrastructure, and it is an issue that warrants investigation to limit the burden of disease from lead exposure.

  10. Regional lead isotope study of a polluted river catchment: River Wear, Northern England, UK.

    Science.gov (United States)

    Shepherd, Thomas J; Chenery, Simon R N; Pashley, Vanessa; Lord, Richard A; Ander, Louise E; Breward, Neil; Hobbs, Susan F; Horstwood, Matthew; Klinck, Benjamin A; Worrall, Fred

    2009-08-15

    High precision, lead isotope analyses of archived stream sediments from the River Wear catchment, northeast England (1986-88), provide evidence for three main sources of anthropogenic lead pollution; lead mining, industrial lead emissions and leaded petrol. In the upper catchment, pollution is totally controlled and dominated by large lead discharges from historic mining centres in the North Pennine Orefield ((208)Pb/(206)Pb, (207)Pb/(206)Pb ratios range from 2.0744-2.0954 and 0.8413-0.8554 respectively). In the lower catchment, co-extensive with the Durham Coalfield and areas of high population density, pollution levels are lower and regionally more uniform. Isotope ratios are systematically higher than in the upper catchment ((208)Pb/(206)Pb, (207)Pb/(206)Pb ratios range from 2.0856-2.1397 and 0.8554-0.8896 respectively) and far exceed values determined for the geogenic regional background. Here, the pollution is characterised by the atmospheric deposition of industrial lead and petrol lead. Lead derived from the combustion of coal, although present, is masked by the other two sources. Recent sediments from the main channel of the River Wear are isotopically indistinguishable from older, low order stream sediments of the North Pennine Orefield, indicating that contamination of the river by lead mining waste (up to several 1000 mg/kg Pb at some locations) continues to pose an environmental problem; a pattern that can be traced all the way to the tidal reach. Using within-catchment isotope variation and sediment lead concentrations, estimates can be made of the discharges from discrete mines or groups of mines to the overall level of lead pollution in the River Wear. As well as providing information pertinent to source apportionment and on-going catchment remediation measures, the database is a valuable resource for epidemiologists concerned with the health risks posed by environmental lead.

  11. Regional lead isotope study of a polluted river catchment: River Wear, Northern England, UK

    Energy Technology Data Exchange (ETDEWEB)

    Shepherd, Thomas J., E-mail: shepherdtj@aol.com [Department of Earth Sciences, University of Durham, Science Laboratories, Durham DH1 3LE (United Kingdom); Chenery, Simon R.N. [British Geological Survey, Nicker Hill, Keyworth, Nottingham NG12 5GG (United Kingdom); Pashley, Vanessa [NERC Isotope Geosciences Laboratory, Kingsley Dunham Centre, Keyworth, Nottingham NG12 5GG (United Kingdom); Lord, Richard A. [School of Science and Technology, University of Teesside, Middlesbrough, Tees Valley TS1 3BA (United Kingdom); Ander, Louise E.; Breward, Neil; Hobbs, Susan F. [British Geological Survey, Nicker Hill, Keyworth, Nottingham NG12 5GG (United Kingdom); Horstwood, Matthew [NERC Isotope Geosciences Laboratory, Kingsley Dunham Centre, Keyworth, Nottingham NG12 5GG (United Kingdom); Klinck, Benjamin A. [British Geological Survey, Nicker Hill, Keyworth, Nottingham NG12 5GG (United Kingdom); Worrall, Fred [Department of Earth Sciences, University of Durham, Science Laboratories, Durham DH1 3LE (United Kingdom)

    2009-08-15

    High precision, lead isotope analyses of archived stream sediments from the River Wear catchment, northeast England (1986-88), provide evidence for three main sources of anthropogenic lead pollution; lead mining, industrial lead emissions and leaded petrol. In the upper catchment, pollution is totally controlled and dominated by large lead discharges from historic mining centres in the North Pennine Orefield ({sup 208}Pb/{sup 206}Pb, {sup 207}Pb/{sup 206}Pb ratios range from 2.0744-2.0954 and 0.8413-0.8554 respectively). In the lower catchment, co-extensive with the Durham Coalfield and areas of high population density, pollution levels are lower and regionally more uniform. Isotope ratios are systematically higher than in the upper catchment ({sup 208}Pb/{sup 206}Pb, {sup 207}Pb/{sup 206}Pb ratios range from 2.0856-2.1397 and 0.8554-0.8896 respectively) and far exceed values determined for the geogenic regional background. Here, the pollution is characterised by the atmospheric deposition of industrial lead and petrol lead. Lead derived from the combustion of coal, although present, is masked by the other two sources. Recent sediments from the main channel of the River Wear are isotopically indistinguishable from older, low order stream sediments of the North Pennine Orefield, indicating that contamination of the river by lead mining waste (up to several 1000 mg/kg Pb at some locations) continues to pose an environmental problem; a pattern that can be traced all the way to the tidal reach. Using within-catchment isotope variation and sediment lead concentrations, estimates can be made of the discharges from discrete mines or groups of mines to the overall level of lead pollution in the River Wear. As well as providing information pertinent to source apportionment and on-going catchment remediation measures, the database is a valuable resource for epidemiologists concerned with the health risks posed by environmental lead.

  12. Lead contamination in cocoa and cocoa products: isotopic evidence of global contamination.

    Science.gov (United States)

    Rankin, Charley W; Nriagu, Jerome O; Aggarwal, Jugdeep K; Arowolo, Toyin A; Adebayo, Kola; Flegal, A Russell

    2005-10-01

    In this article we present lead concentrations and isotopic compositions from analyses of cocoa beans, their shells, and soils from six Nigerian cocoa farms, and analyses of manufactured cocoa and chocolate products. The average lead concentration of cocoa beans was cocoa and chocolate products were as high as 230 and 70 ng/g, respectively, which are consistent with market-basket surveys that have repeatedly listed lead concentrations in chocolate products among the highest reported for all foods. One source of contamination of the finished products is tentatively attributed to atmospheric emissions of leaded gasoline, which is still being used in Nigeria. Because of the high capacity of cocoa bean shells to adsorb lead, contamination from leaded gasoline emissions may occur during the fermentation and sun-drying of unshelled beans at cocoa farms. This mechanism is supported by similarities in lead isotopic compositions of cocoa bean shells from the different farms (206Pb/207Pb = 1.1548-1.1581; 208Pb/207Pb = 2.4344-2.4394) with those of finished cocoa products (206Pb/207Pb = 1.1475-1.1977; 208Pb/207Pb = 2.4234-2.4673). However, the much higher lead concentrations and larger variability in lead isotopic composition of finished cocoa products, which falls within the global range of industrial lead aerosols, indicate that most contamination occurs during shipping and/or processing of the cocoa beans and the manufacture of cocoa and chocolate products.

  13. Rapid isotopic changes in groundwater, upper Rio Guanajuato catchment, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Cortes, Alejandra; Durazo, Jaime [Departamento de recursos naturales, Instituto de Geofisica, Universidad Nacional Autonoma de Mexico, Mexico, D.F. (Mexico); Kralisch, Stefanie [Posgrado en Ciencias de la Tierra, Universidad Nacional Autonoma de Mexico, Mexico, D.F. (Mexico)

    2007-01-15

    Significant changes in the isotopic composition of groundwater in the upper catchment of Rio Guanajuato, Mexico, were detected in two independent sets of samplers for 3 % of the 1600 high-production wells in the area. Sampling was done in December 1998 (53 samples), and in July - August 2003 (41 samples). Average deuterium concentration did not change between 1998 and 2003 but the average oxygen-18 concentration suggested a generalized dilution from deep water from infiltrated local precipitation. This regional change occurred within 56 months, indicating a highly dynamic hydrogeologic system. Fast replenishment of aquifer storage, or non sustainable over-pumping of old aquifer reserves, are possible explanations. [Spanish] Cambios isotopicos significativos en el agua subterranea de la cuenca alta del Rio Guanajuato, Mexico, fueron detectados en dos conjuntos independientes de muestras que incluyeron al 3% de los 1600 pozos de alta produccion del area. Los muestreos se realizaron en diciembre de 1998 (53 muestras) y en julio - agosto del 2003 (41 muestras). La concentracion promedio del deuterio no cambio entre 1998 y 2003, pero la del oxigeno-18 sugiere una dilucion generalizada del agua profunda por infiltracion de la precipitacion local. Este cambio regional ocurrio dentro de 56 meses, indicando un sistema hidrogeologico muy dinamico. La rapida recuperacion del almacenamiento acuifero o el bombeo insostenible de reservas acuiferas viejas son explicaciones posibles.

  14. RAPID SEPARATION METHOD FOR 237NP AND PU ISOTOPES IN LARGE SOIL SAMPLES

    Energy Technology Data Exchange (ETDEWEB)

    Maxwell, S.; Culligan, B.; Noyes, G.

    2010-07-26

    A new rapid method for the determination of {sup 237}Np and Pu isotopes in soil and sediment samples has been developed at the Savannah River Site Environmental Lab (Aiken, SC, USA) that can be used for large soil samples. The new soil method utilizes an acid leaching method, iron/titanium hydroxide precipitation, a lanthanum fluoride soil matrix removal step, and a rapid column separation process with TEVA Resin. The large soil matrix is removed easily and rapidly using this two simple precipitations with high chemical recoveries and effective removal of interferences. Vacuum box technology and rapid flow rates are used to reduce analytical time.

  15. Contaminated lead environments of man: reviewing the lead isotopic evidence in sediments, peat, and soils for the temporal and spatial patterns of atmospheric lead pollution in Sweden.

    Science.gov (United States)

    Bindler, Richard

    2011-08-01

    Clair Patterson and colleagues demonstrated already four decades ago that the lead cycle was greatly altered on a global scale by humans. Moreover, this change occurred long before the implementation of monitoring programs designed to study lead and other trace metals. Patterson and colleagues also developed stable lead isotope analyses as a tool to differentiate between natural and pollution-derived lead. Since then, stable isotope analyses of sediment, peat, herbaria collections, soils, and forest plants have given us new insights into lead biogeochemical cycling in space and time. Three important conclusions from our studies of lead in the Swedish environment conducted over the past 15 years, which are well supported by extensive results from elsewhere in Europe and in North America, are: (1) lead deposition rates at sites removed from major point sources during the twentieth century were about 1,000 times higher than natural background deposition rates a few thousand years ago (~10 mg Pb m(-2) year(-1) vs. 0.01 mg Pb m(-2) year(-1)), and even today (~1 mg Pb m(-2) year(-1)) are still almost 100 times greater than natural rates. This increase from natural background to maximum fluxes is similar to estimated changes in body burdens of lead from ancient times to the twentieth century. (2) Stable lead isotopes ((206)Pb/(207)Pb ratios shown in this paper) are an effective tool to distinguish anthropogenic lead from the natural lead present in sediments, peat, and soils for both the majority of sites receiving diffuse inputs from long range and regional sources and for sites in close proximity to point sources. In sediments >3,500 years and in the parent soil material of the C-horizon, (206)Pb/(207)Pb ratios are higher, 1.3 to >2.0, whereas pollution sources and surface soils and peat have lower ratios that have been in the range 1.14-1.18. (3) Using stable lead isotopes, we have estimated that in southern Sweden the cumulative anthropogenic burden of

  16. Lead isotopic compositions of common arsenical pesticides used in New England

    Science.gov (United States)

    Ayuso, Robert; Foley, Nora; Robinson, Gilpin; Wandless, Gregory; Dillingham, Jeremy

    2004-01-01

    The three most important arsenical pesticides and herbicides that were extensively used on apple, blueberry, and potato crops in New England from mid-1800s to recent times are lead arsenate, calcium arsenate, and sodium arsenate. Lead arsenate was probably the most heavily used of the arsenical pesticides until it was banned in 1988. Other metal-arsenic pesticides were also used but in lesser amounts. A recent report identified areas in New England where arsenical pesticides were used extensively (Robinson and Ayuso, 2004). On the basis of factor analysis of metal concentrations in stream sediment samples, a positive correlation with pesticide use was shown in regions having stream sediment sample populations that contained concentrations of high arsenic and lead. Lead isotope compositions of stream sediments from areas with heavy use of the pesticides could not be entirely explained by lead originating from rock sulfides and their weathering products. An industrial lead contribution (mostly from atmospheric deposition of lead) was suggested in general to explain the lead isotopic distributions of the stream sediments that could not be accounted for by the natural lead in the environment. We concluded that when agricultural land previously contaminated with arsenical pesticides is urbanized, pesticide residues in the soils and stream sediments could be released into the groundwater. No lead isotopic data characterizing the compositions of pesticides were available for comparison. We have determined the lead isotopic compositions of commonly used pesticides in New England, such as lead arsenate, sodium metaarsenite, and calcium arsenate, in order to assist in future isotopic comparisons and to better establish anthropogenic sources of Pb and As. New data are also presented for copper acetoarsenite (or Paris green), methyl arsonic acid and methane arsonic acid, as well as for arsanilic acid, all of which are used as feed additives to promote swine and poultry growth

  17. Lead isotope systematics of some igneous rocks from the Egyptian Shield

    Science.gov (United States)

    Gillespie, J. G.; Dixon, T. H.

    1983-01-01

    Lead isotope data on whole-rock samples and two feldspar separates for a variety of Pan-African (late Precambrian) igneous rocks for the Egyptian Shield are presented. It is pointed out that the eastern desert of Egypt is a Late Precambrian shield characterized by the widespread occurrence of granitic plutons. The lead isotope ratios may be used to delineate boundaries between Late Precambrian oceanic and continental environments in northeastern Africa. The samples belong to three groups. These groups are related to a younger plutonic sequence of granites and adamellites, a plutonic group consisting of older tonalites to granodiorites, and the Dokhan volcanic suite.

  18. Temporal variations in lead concentrations and isotopic composition in the Southern California Bight

    Energy Technology Data Exchange (ETDEWEB)

    Sanudo-Wilhelmy, S.A.; Flegal, A.R. (Univ. of California, Santa Cruz, CA (United States))

    1994-08-01

    Lead concentrations in surface waters of the Southern California Bight appear to have decreased threefold (from >170 to <60 pM) since they were initially measured by Clair Patterson and his associates in the 1970s. The decrease parallels a threefold decline in anthropogenic inputs of industrial lead to the bight over the past two decades. Moreover, mass balance calculations indicate that the primary source of lead to the bight now is upwelling. This is evidenced by the isotopic compositions of surface waters in the bight, which are most characteristic of Asian industrial lead aerosols (0.4793 [le] [sup 206]Pb/[sup 208]Pb [le] 0.4833) deposited in oceanic waters of the North Pacific. While the decrease in surface water lead concentrations in the bight reflects the reduction in industrial lead emissions from the United States, the isotopic compositions of surface waters in the southern reach of the bight reflect a concurrent increase in industrial lead emissions from Mexico (0.4852 [le] [sup 206]Pb/[sup 208]Pb [le] 0.4877). The isotopic composition ([sup 208]Pb/[sup 207]Pb [approximately] 2.427) of elevated lead concentrations of surface waters in San Diego Bay indicate that lead is being remobilized from contaminated sediments within that bay.

  19. Lead isotopes in sediments of the Loire River (France): natural versus anthropogenic origin

    Science.gov (United States)

    Negrel, Ph.; Petelet-Giraud, E.

    2012-04-01

    Sediments along the Loire River (central France) were investigated by means of lead isotopes determined on the labile sediment fraction, or acid-extractable matter (AEM). The combination of trace elements and lead isotopes allows deciphering the origin of the elements (i.e. natural or anthropogenic) and their history, both in the sediment and soil from two small watersheds (one draining basalt, the other one granite-gneiss gneiss in the upper part of the catchment), in present-day suspended matter in Loire River water, and in sediment from the Loire estuary. Fe-Mn oxides act as the main carrier phase of the elements in the AEM extracted by cold HBr, Th and Pb concentrations were determined by ICP-MS and lead isotopes by ICP-MS-MC Neptune. Thorium displays mostly insoluble behaviour in hydrosystems, but the small amount of dissolved Th shows a strong tendency to be adsorbed onto oxyhydroxides. Therefore, Mn and Th (as well as other trace elements) correlate well in AEM, the correlations of Mn, and Pb with Th as a typical indicator of crustal weathering points to their derivation from the silicate basement of the upstream part of the catchment. Crustal weathering, as confirmed by the Pb-isotope ratios for most sample points, is the main natural source of lead in the upstream part of the Loire River, as well as that transported in the middle part of the basin and up to the estuary. Among anthropogenic sources, the use of Pb-isotopic compositions shows an influence of agricultural lead-derived inputs and a large input from lead as a gasoline additive, particularly in the estuary due to harbour activities and for one downstream tributary river that is strongly marked by this type of lead input.

  20. Lead shot contribution to blood lead of First Nations people: The use of lead isotopes to identify the source of exposure

    Energy Technology Data Exchange (ETDEWEB)

    Tsuji, Leonard J.S. [Department of Environment and Resource Studies, University of Waterloo, Waterloo, Ontario, N2L 3G1 (Canada)], E-mail: ljtsuji@fes.uwaterloo.ca; Wainman, Bruce C. [Faculty of Health Sciences, McMaster University, Hamilton, Ontario, L8N 3Z5 (Canada); Martin, Ian D. [Department of Environment and Resource Studies, University of Waterloo, Waterloo, Ontario, N2L 3G1 (Canada); Sutherland, Celine [Attawapiskat First Nation Health Services, Attawapiskat, Ontario, P0L 1A0 (Canada); Weber, Jean-Philippe; Dumas, Pierre [Centre de toxicologie, Institut national de sante publique du Quebec, Quebec City, Quebec, G1V 5B3 (Canada); Nieboer, Evert [Faculty of Health Sciences, McMaster University, Hamilton, Ontario, L8N 3Z5 (Canada); Institute of Community Medicine, University of Tromso, Tromso N-9037 (Norway)

    2008-11-01

    Although lead isotope ratios have been used to identify lead ammunition (lead shotshell pellets and bullets) as a source of exposure for First Nations people of Canada, the actual source of lead exposure needs to be further clarified. Whole blood samples for First Nations people of Ontario, Canada, were collected from participants prior to the traditional spring harvest of water birds, as well as post-harvest. Blood-lead levels and stable lead isotope ratios prior to, and after the harvest were determined by ICP-MS. Data were analyzed by paired t-tests and Wilcoxon Signed-Ranks tests. All participants consumed water birds harvested with lead shotshell during the period of study. For the group excluding six males who were potentially exposed to other sources of lead (as revealed through a questionnaire), paired t-tests and Wilcoxon Signed-Ranks tests showed consistent results: significant (p < 0.05) increases in blood-lead concentrations and blood levels of {sup 206}Pb/{sup 204}Pb and {sup 206}Pb/{sup 207}Pb towards the mean values we previously reported for lead shotshell pellets; and a significant decrease in {sup 208}Pb/{sup 206}Pb values towards the mean for lead shotshell pellets. However, when we categorized the group further into a group that did not use firearms and did not eat any other traditional foods harvested with lead ammunition other than waterfowl, our predictions for {sup 206}Pb/{sup 204}Pb, {sup 206}Pb/{sup 207}Pb and {sup 208}Pb/{sup 206}Pb hold true, but there was not a significant increase in blood-lead level after the hunt. It appears that the activity of hunting (i.e., use of a shotgun) was also an important route of lead exposure. The banning of lead shotshell for all game hunting would eliminate a source of environmental lead for all people who use firearms and/or eat wild game.

  1. Lead shot contribution to blood lead of First Nations people: the use of lead isotopes to identify the source of exposure.

    Science.gov (United States)

    Tsuji, Leonard J S; Wainman, Bruce C; Martin, Ian D; Sutherland, Celine; Weber, Jean-Philippe; Dumas, Pierre; Nieboer, Evert

    2008-11-01

    Although lead isotope ratios have been used to identify lead ammunition (lead shotshell pellets and bullets) as a source of exposure for First Nations people of Canada, the actual source of lead exposure needs to be further clarified. Whole blood samples for First Nations people of Ontario, Canada, were collected from participants prior to the traditional spring harvest of water birds, as well as post-harvest. Blood-lead levels and stable lead isotope ratios prior to, and after the harvest were determined by ICP-MS. Data were analyzed by paired t-tests and Wilcoxon Signed-Ranks tests. All participants consumed water birds harvested with lead shotshell during the period of study. For the group excluding six males who were potentially exposed to other sources of lead (as revealed through a questionnaire), paired t-tests and Wilcoxon Signed-Ranks tests showed consistent results: significant (plead concentrations and blood levels of (206)Pb/(204)Pb and (206)Pb/(207)Pb towards the mean values we previously reported for lead shotshell pellets; and a significant decrease in (208)Pb/(206)Pb values towards the mean for lead shotshell pellets. However, when we categorized the group further into a group that did not use firearms and did not eat any other traditional foods harvested with lead ammunition other than waterfowl, our predictions for (206)Pb/(204)Pb, (206)Pb/(207)Pb and (208)Pb/(206)Pb hold true, but there was not a significant increase in blood-lead level after the hunt. It appears that the activity of hunting (i.e., use of a shotgun) was also an important route of lead exposure. The banning of lead shotshell for all game hunting would eliminate a source of environmental lead for all people who use firearms and/or eat wild game.

  2. Tracing lead pollution sources in abandoned mine areas using stable Pb isotope ratios.

    Science.gov (United States)

    Yoo, Eun-Jin; Lee, Jung-A; Park, Jae-Seon; Lee, Khanghyun; Lee, Won-Seok; Han, Jin-Seok; Choi, Jong-Woo

    2014-02-01

    This study focused on Pb isotope ratios of sediments in areas around an abandoned mine to determine if the ratios can be used as a source tracer. For pretreatment, sediment samples were dissolved with mixed acids, and a multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS, Nu plasma II) was used to investigate the Pb isotopic composition of the samples. The measured isotope ratios were then corrected for instrumental mass fractionation by measuring the (203)Tl/(205)Tl ratio. Repeated measurements with the NIST SRM 981 reference material showed that the precision of all ratios was below 104 ppm (±2σ) for 50 ng/g. The isotope ratios ((207)Pb/(206)Pb) found were 0.85073 ± 0.0004~0.85373 ± 0.0003 for the main stream, while they were 0.83736 ± 0.0010 for the tributary and 0.84393 ± 0.0002 for the confluence. A binary mixing equation for isotope ratios showed that the contributions of mine lead to neighboring areas were up to 60%. Therefore, Pb isotope ratios can be a good source tracer for areas around abandoned mines.

  3. Identification of historical lead sources in roof dusts and recent lake sediments from an industrialized area: indications from lead isotopes.

    Science.gov (United States)

    Chiaradia, M; Chenhall, B E; Depers, A M; Gulson, B L; Jones, B G

    1997-10-20

    X-ray fluorescence and stable lead (Pb) isotopic analyses have been undertaken on dusts, known from microscopic investigation to contain significant quantities of industrially- and urban-derived particulate matter, present in the roof cavities of houses in the Illawarra region (N.S.W., Australia), with the objective of examining the historic record of Pb pollution. All investigated houses contained in excess of 250 micrograms g-1 Pb, with dwellings close to a copper smelter, in a large industrial complex including a major steelworks, containing higher (> 2500 micrograms g-1) Pb concentrations. The isotopic composition in the dusts, expressed here as 206Pb/204Pb, is relatively constant at 17.0, irrespective of dwelling age or distance from the industrial complex. Contamination of the dusts by Pb sourced from paint cannot explain the isotopic uniformity of the dust samples. Isotopic modelling indicates that the dusts contain Pb derived from the copper smelter, gasoline-air Pb and a minor contribution from coal-utilising sources. Lead loading was also investigated in the adjacent lagoon, which acts as a natural sink for particulate matter in the Illawarra region. Isotopic data and modelling indicate that one natural and four anthropogenic sources contribute to the Pb burden of this lagoon. The natural source consists of Permian rocks cropping out in the catchment area which have a 206Pb/204Pb of approximately 18.7. The suggested anthropogenic sources are an old disbanded base-metal (Pb) smelter (206Pb/204Pb approximately 16.2-16.3), the copper smelter (206Pb/204Pb approximately 17.9), gasoline-air derived Pb (206Pb/204Pb approximately 16.4-16.5) and industries utilising coal, for example the recently closed thermal coal-fired power station (206Pb/204Pb approximately 18.9). The relative contributions of the base-metal (mainly lead) smelter and gasoline-air Pb in the sediment can only be partly assessed due to the isotopic similarity of these sources. Likewise the

  4. Microcalorimeter Q-spectroscopy for rapid isotopic analysis of trace actinide samples

    Energy Technology Data Exchange (ETDEWEB)

    Croce, M.P., E-mail: mpcroce@lanl.gov [Los Alamos National Laboratory, Los Alamos, NM (United States); Bond, E.M.; Hoover, A.S.; Kunde, G.J.; Mocko, V.; Rabin, M.W.; Weisse-Bernstein, N.R.; Wolfsberg, L.E. [Los Alamos National Laboratory, Los Alamos, NM (United States); Bennett, D.A.; Hays-Wehle, J.; Schmidt, D.R.; Ullom, J.N. [National Institute of Standards and Technology, Boulder, CO (United States)

    2015-06-01

    We are developing superconducting transition-edge sensor (TES) microcalorimeters that are optimized for rapid isotopic analysis of trace actinide samples by Q-spectroscopy. By designing mechanically robust TESs and simplified detector assembly methods, we have developed a detector for Q-spectroscopy of actinides that can be assembled in minutes. We have characterized the effects of each simplification and present the results. Finally, we show results of isotopic analysis of plutonium samples with Q-spectroscopy detectors and compare the results to mass spectrometry.

  5. Lead isotopic evidence for evolutionary changes in magma-crust interaction, Central Andes, southern Peru

    Energy Technology Data Exchange (ETDEWEB)

    Barreiro, B.A. (California Univ., Santa Barbara (USA). Dept. of Geological Sciences); Clark, A.H. (Queen' s Univ., Kingston, Ontario (Canada). Dept. of Geological Sciences)

    1984-07-01

    Lead isotopic measurements were made on Andean igneous rocks of Jurassic to Recent age in Moquegua and Tacna Departments, southernmost Peru, to clarify the petrogenesis of the rocks and, in particular, to investigate the effect of crustal thickness on rock composition. This location in the Cordillera Occidental is ideal for such a study because the ca. 2 Ga Precambrian basement rocks (Arequipa massif) have a distinct Pb isotopic signature which is an excellent tracer of crustal interaction, and because geomorphological research has shown that the continental crust was here thickened drastically in the later Tertiary.

  6. Insights into past atmospheric lead emissions using lead concentrations and isotopic compositions in historic lichens and fungi (1852-2008) from central and southern Victoria, Australia

    Science.gov (United States)

    Wu, Liqin; Taylor, Mark Patrick; Handley, Heather K.; Gulson, Brian L.

    2016-08-01

    Lead concentrations and lead isotopic compositions were determined in historic central and southern Victoria, Australia lichen (Cladonia and Usnea) and fungi (Trametes) samples collected between 1852 and 2008 to evaluate long-term atmospheric lead contamination sources. The data are grouped into four time intervals of 1850-1931, 1932-1984, 1985-2001 and 2002-2008 corresponding to the history of leaded petrol use in Australia. Elevated lichen and fungi lead concentrations and relatively high isotopic compositions from the period 1850-1931 are attributed to lithogenic sources, gold mining activities and early industrialisation. Significant increases in lichen and fungi lead concentrations and concomitant lower lead isotopic compositions correspond to the marked increase in lead emissions from leaded petrol use after 1932. Following the end of leaded petrol use in 2002 lead isotopic composition values 'recover' toward more lithogenic values. However, the lead isotopic composition data indicate that the environmental impact from leaded petrol emissions persists in contemporary samples dated to 2002-2008. Overall, the data reveal that herbarium lichens and fungi from central and southern Victoria can be used as proxies for environmental lead emissions over the past 150 years.

  7. Ancient bronze coins from Mediterranean basin: LAMQS potentiality for lead isotopes comparative analysis with former mineral

    Energy Technology Data Exchange (ETDEWEB)

    Torrisi, L., E-mail: Lorenzo.Torrisi@unime.it [Department of Physics Science - MIFT, Messina University, V.le F.S. d’Alcontres 31, 98166 S. Agata, Messina (Italy); Italiano, A. [INFN, Sezione di Catania, Gruppo collegato di Messina (Italy); Torrisi, A. [Institute of Optoelectronics, Military University of Technology, 2 Kaliskiego Str., 00-908 Warsaw (Poland)

    2016-11-30

    Highlights: • Surface and bulk compositional elements in ancient bronze coins were investigated using XRF analysis. • Lead stable isotope {sup 204}Pb, {sup 206}Pb, {sup 207}Pb and {sup 208}Pb were measured in ancient coins with LAMQS analysis. • Lead ratios {sup 208}Pb/{sup 206}Pb and {sup 207}Pb/{sup 206}Pb, measured by LAMQS, were compared with Brettscaife.net geological database relative to the minerals in different mines of Mediterranean basin. • Bronze coins were correlated to possible ancient mining sites of minerals from which lead was extracted. - Abstract: Bronze coins coming from the area of the Mediterranean basin, dated back the II–X Cent. A.D., were analyzed using different physical analytical techniques. Characteristic X-ray fluorescence was used with electrons and photons, in order to investigate the elemental composition of both the surface layers and bulk. Moreover, the quadrupole mass spectrometry coupled to laser ablation (LAMQS technique) in high vacuum was used to analyse typical material compounds from surface contamination. Mass spectrometry, at high resolution and sensitivity, extended up to 300 amu, allowed measuring the {sup 208}Pb/{sup 206}Pb and {sup 207}Pb/{sup 206}Pb isotopic ratios into the coins. Quantitative relative analyses of these isotopic ratios identify the coin composition such as a “fingerprint” depending on the mineral used to extract the lead. Isotopic ratios in coins can be compared to those of the possible minerals used to produce the bronze alloy. A comparison between the measured isotope ratios in the analyzed coins and the literature database, related to the mineral containing Pb as a function of its geological and geophysical extraction mine, is presented. The analysis, restricted to old coins and the mines of the Mediterranean basin, indicates a possible correlation between the coin compositions and the possible geological sites of the extracted mineral.

  8. Sulfur and lead isotopic evidence of relic Archean sediments in the Pitcairn mantle plume

    Science.gov (United States)

    Delavault, Hélène; Chauvel, Catherine; Thomassot, Emilie; Devey, Colin W.; Dazas, Baptiste

    2016-11-01

    The isotopic diversity of oceanic island basalts (OIB) is usually attributed to the influence, in their sources, of ancient material recycled into the mantle, although the nature, age, and quantities of this material remain controversial. The unradiogenic Pb isotope signature of the enriched mantle I (EM I) source of basalts from, for example, Pitcairn or Walvis Ridge has been variously attributed to recycled pelagic sediments, lower continental crust, or recycled subcontinental lithosphere. Our study helps resolve this debate by showing that Pitcairn lavas contain sulfides whose sulfur isotopic compositions are affected by mass-independent fractionation (S-MIF down to Δ33S = -0.8), something which is thought to have occurred on Earth only before 2.45 Ga, constraining the youngest possible age of the EM I source component. With this independent age constraint and a Monte Carlo refinement modeling of lead isotopes, we place the likely Pitcairn source age at 2.5 Ga to 2.6 Ga. The Pb, Sr, Nd, and Hf isotopic mixing arrays show that the Archean EM I material was poor in trace elements, resembling Archean sediment. After subduction, this Archean sediment apparently remained stored in the deep Earth for billions of years before returning to the surface as Pitcairńs characteristic EM I signature. The presence of negative S-MIF in the deep mantle may also help resolve the problem of an apparent deficit of negative Δ33S anomalies so far found in surface reservoirs.

  9. Use of isotope ratios to identify sources contributing to pediatric lead poisoning in Peru.

    Science.gov (United States)

    Naeher, Luke P; Rubin, Carol S; Hernandez-Avila, Mauricio; Noonan, Gary P; Paschal, Dan; Narciso, Juan; Lain, Rocio Espinoza; Gastanaga, Carmen; Almeyda, Rosa; Jarrett, Jeff; Caldwell, Kathleen L; McGeehin, Michael

    2003-09-01

    In 1998, a school-based blood lead level (BLL) survey of 2,510 children, conducted in Lima and Callao, Peru, revealed elevated BLLs in children from 2 Callao schools (mean BLL = 25.6 microg/dl; n = 314) and in children from Callao overall (mean BLL = 15.2 microg/dl; n = 898), compared with children from Lima (mean BLL = 7.1 microg/dl; n = 1,612). Public health officials at Peru's Direccion General de Salud Ambiental (DIGESA) hypothesized that a possible source of the elevated pediatric BLLs observed in Callao was a large depository near the port where mineral concentrates are stored prior to shipment. The U.S. Centers for Disease Control and Prevention worked with DIGESA to identify source(s) that contributed to the pediatric lead poisonings by comparing isotopic profiles of lead in blood, mineral, gasoline, and air filter samples. The lead isotope ratio (IR) observed in mineral samples from the depository in Callao differed from those in gasoline samples from Lima and Callao. The blood lead IRs of children living near the depository were similar to the IRs of the mineral samples and different from the IRs of the gasoline samples, suggesting that lead from the depository-and not gasoline-was the primary source of lead in these children. Lead IR analysis of regional air filter samples supported these findings.

  10. Lead Contamination in Cocoa and Cocoa Products: Isotopic Evidence of Global Contamination

    OpenAIRE

    Rankin, Charley W.; Nriagu, Jerome O.; Aggarwal, Jugdeep K.; Arowolo, Toyin A.; Adebayo, Kola; Flegal, A. Russell

    2005-01-01

    In this article we present lead concentrations and isotopic compositions from analyses of cocoa beans, their shells, and soils from six Nigerian cocoa farms, and analyses of manufactured cocoa and chocolate products. The average lead concentration of cocoa beans was ≤ 0.5 ng/g, which is one of the lowest reported values for a natural food. In contrast, lead concentrations of manufactured cocoa and chocolate products were as high as 230 and 70 ng/g, respectively, which are consistent with mark...

  11. Lead concentration and isotope chronology in two coastal environments in Western and South East Asia

    Science.gov (United States)

    Carrasco, G. G.; Chen, M.; Boyle, E. A.; Zhao, N.; Nurhati, I. S.; Gevao, B.; al Ghadban, A.; Switzer, A.; Lee, J. M.

    2014-12-01

    Lead is a trace metal that is closely related to anthropogenic activity, mainly via leaded gasoline and coal combustion. The study of lead concentrations and isotopes in seawater, sediments, corals and aerosols allows for a systematic look at its sources and their time evolution in a natural environment. We will discuss results from two projects in Western and South East Asia, regions that have seen dramatic socio-economical changes over the past half-century that may have left environmental signals. These results highlight the usefulness of the method, indicate the degree of complexity of these systems, and point to the need for a continuous monitoring of anthropogenic trace metals in the small-medium coastal scale to be able to asses the larger scale effects of human activity. On the one hand, coastal Kuwait is heavily influenced by the Shat al-Arab river and shows a clear anthropogenic signature from Kuwait city. A mix of two sources can be tracked through the coral and sediment chronological records, with Pb206/Pb207 ratios (1.202 and 1.151) that approach the suspected source values (1.21 and 1.12) and eliminate the possibility of other sources. Through a wide sediment geographic distribution, the strength of the anthropogenic signature is modulated. On the other hand, Singapore offers a more complex system, where an apparent mix of two sources (extreme isotope ratios 1.215 and ~1.14) occurs also, but where either an unresolved potentially important third source (isotope ratio ~1.18), or an isotope exchange process should be invoked. The sediment and coral records allows us to track the changes through time; however, there seems to be incongruence with the aerosol isotope record. Further potential sources are being explored currently and will be discussed.

  12. GEMAS: a new view of the lead isotopic soil landscape at the European continental scale

    Science.gov (United States)

    Reimann, Clemens; Négrel, Philippe; Flem, Belinda; Fabian, Karl; Birke, Manfred; Ladenberger, Anna; Hoogewerff, Jurian

    2014-05-01

    Soil formation through weathering of bedrock and sediments is an extremely slow process, and soils must be considered an essential and non-renewable resource. Knowledge and extrapolation of threats to soils, e.g., changes in element concentrations and the reasons thereof are of primary importance for society as recently diffuse contamination has been identified as one of the major threats to soil quality. In this frame the addition of isotope tracing at the continental scale is an important supplementary constraint on the origin and behaviour of elements in soils. Lead has been mined and utilized by humans for several thousand years. The accumulated world production is estimated to be over 300 Mt. Detailed studies on environmental samples (e.g., peat bogs, ice cores, sediment cores) suggest a major Pb contamination of the northern hemisphere since ancient times. In spite of its importance the continental scale distribution of lead and lead isotopes combined has never been documented for any geochemical sample material. As the result of a combined effort of the European Geological Surveys, backed by the European metals industry, we present the first continental investigation of Pb concentration and Pb isotope ratios (206Pb,207Pb, 208Pb) landscape using agricultural soil samples (Ap-horizon, 0-20 cm) collected at an average density of 1 site/2500 km2 (2211 samples in total). Thus we here provide the first geochemical reference maps of Pb concentrations combined with Pb isotope ratios at the European scale against which the impact of contamination can be realistically judged. The maps localize the major concentration anomalies of Pb in soils and help to identify the processes that generate the observed distribution patterns. The European continental-scale patterns of Pb concentrations and Pb isotopes show a high variability dominated by geology and influenced by climate. Positive Pb concentration anomalies mark most of the known mineralized areas throughout Europe

  13. Zn/Cd ratios and cadmium isotope evidence for the classification of lead-zinc deposits.

    Science.gov (United States)

    Wen, Hanjie; Zhu, Chuanwei; Zhang, Yuxu; Cloquet, Christophe; Fan, Haifeng; Fu, Shaohong

    2016-04-28

    Lead-zinc deposits are often difficult to classify because clear criteria are lacking. In recent years, new tools, such as Cd and Zn isotopes, have been used to better understand the ore-formation processes and to classify Pb-Zn deposits. Herein, we investigate Cd concentrations, Cd isotope systematics and Zn/Cd ratios in sphalerite from nine Pb-Zn deposits divided into high-temperature systems (e.g., porphyry), low-temperature systems (e.g., Mississippi Valley type [MVT]) and exhalative systems (e.g., sedimentary exhalative [SEDEX]). Our results showed little evidence of fractionation in the high-temperature systems. In the low-temperature systems, Cd concentrations were the highest, but were also highly variable, a result consistent with the higher fractionation of Cd at low temperatures. The δ(114/110)Cd values in low-temperature systems were enriched in heavier isotopes (mean of 0.32 ± 0.31‰). Exhalative systems had the lowest Cd concentrations, with a mean δ(114/110)Cd value of 0.12 ± 0.50‰. We thus conclude that different ore-formation systems result in different characteristic Cd concentrations and fraction levels and that low-temperature processes lead to the most significant fractionation of Cd. Therefore, Cd distribution and isotopic studies can support better understanding of the geochemistry of ore-formation processes and the classification of Pb-Zn deposits.

  14. Lead isotope and trace element composition of urban soils in Mongolia

    Science.gov (United States)

    Tserenpil, Sh.; Sapkota, A.; Liu, C.-Q.; Peng, J.-H.; Liu, B.; Segebade, P. Chr.

    2016-08-01

    Lead (Pb) pollution in and around Ulaanbaatar is of national concern, given that the Mongolian capital is home to nearly half of the country's entire population. By comparison, Mongolian countryside is a pristine environment because of its sparse population and low industrial activity. The concentration of Pb in urban soils (average of 39.1 mg kg-1) was twice the values found (average 18.6 mg kg-1) in background territories (i.e., Mongolian rural sites). Furthermore, Pb contamination was examined by using Pb stable isotopic composition, and covariance of Pb isotopic ratios showed two groups between rural and urban soils as pristine and disturbed sites. The 206Pb/207Pb ratio, the most prominent fingerprint for Pb pollution, was 1.163-1.185 for the urban whereas values for rural soils (1.186-1.207) were analogue to the regional Pb isotopic signatures. Local coal sources and their combustion products, one of the potential Pb pollution sources in Ulaanbaatar, have significant radiogenic properties in terms of Pb isotopic composition and revealed an average of 1.25 for 206Pb/207Pb and 19.551 for 206Pb/204Pb ratios. Thus, contributions from coal firing activity to Pb pollution lower than it was assumed, and smaller range of these values measured in urban soils may be attributed to the mixing of less radiogenic Pb as a constituent of the leaded gasolines.

  15. Lead isotope composition of Central American volcanoes: Influence of the Galapagos plume

    Science.gov (United States)

    Feigenson, Mark D.; Carr, Michael J.; Maharaj, Susan V.; Juliano, Scott; Bolge, Louise L.

    2004-06-01

    Lead isotopic analyses of lavas from Central America, both along and behind the volcanic arc, help to clarify source components in the mantle wedge. Analysis of previous Pb isotopic data had implied that little or no marine sediment lead was added to the Central American source region, as all samples fell within the MORB field, in contrast to other information (e.g., Ba/La, 10Be, 87Sr/86Sr) that indicated a high subduction component. The data presented here include several analyses of local marine sediment, showing it to be exceptionally unradiogenic in Pb and thus permitting high sediment contributions to the mantle source region without significant changes in Pb isotopes. Combined Pb-Nd and Pb-Sr isotopic diagrams clearly illustrate the influence of crustal contamination for samples from Guatemala and Honduras, and of subducted sediment for all lavas of the volcanic front. Samples collected behind the volcanic front are derived from mixing between enriched and depleted mantle sources, and in central Costa Rica (extending to the back arc) overlap Pb, Sr and Nd isotope values for both Cocos Island and some components of the Galapagos hot spot. The restricted geographical occurrence of the enriched mantle signature in Central America, coupled with the persistence of the signal well into the back arc region, imply that these lavas are sampling Galapagos plume-influenced mantle. The presence of this plume component beneath southern Central America and extending to the northeast beneath the Caribbean confirms a Galapagos hot spot origin for this part of Caribbean Plate.

  16. Lead isotopic studies of lunar soils - Their bearing on the time scale of agglutinate formation

    Science.gov (United States)

    Church, S. E.; Tilton, G. R.; Chen, J. H.

    1976-01-01

    Fines (smaller than 75 microns) and bulk soil were studied to analyze loss of volatile lead; losses of the order of 10% to 30% radiogenic lead during the production of agglutinates are assessed. Lead isotope data from fine-agglutinate pairs are analyzed for information on the time scale of micrometeorite bombardment, from the chords generated by the data in concordia diagrams. Resulting mean lead loss ages were compared to spallogenic gas exposure ages for all samples. Labile parentless radiogenic Pb residing preferentially on or in the fines is viewed as possibly responsible for aberrant lead loss ages. Bulk soils plot above the concordia curve (in a field of excess radiogenic Pb) for all samples with anomalous ages.

  17. Copper and lead isotopic and metallic pollution record in soils from the Kombat mining area, Namibia

    Science.gov (United States)

    Mihaljevic, Martin; Ettler, Vojtech; Vanek, Ales; Chrastny, Vladislav; Kribek, Bohdan; Penizek, Vit; Sracek, Ondrej

    2013-04-01

    Copper (Cu) and lead (Pb) concentration, isotopic composition (206Pb/207Pb, 65Cu/63Cu) and speciation were studied in soils from the Kombat mining area. The Cu and Pb concentrations in the studied soils ranged between 21 mg/kg - 757 mg/kg, and 19 mg/kg - 815 mg/kg respectively. In the sequential extractions, the largest part of soil Cu appeared in the residual and reducible fractions and Pb was predominantly bound in reducible and residual fractions and was more mobile compared to Cu. Copper and Pb concentration are higher in soils close to the slime deposit. Concentration of both metals increased with increasing soil depth in irrigated and cultivated soils. In soils not contaminated by dust eroded from the slime deposit, Cu and Pb contents are not dependent on the soil depth. The Pb isotopic signatures (206Pb/207Pb) ranged between 1.15 - 1.21 in soils from the Kombat area. In most of soil samples, surface horizons exhibited lower 206Pb/207Pb ratio, which originates from the slime dust pollution (206Pb/207Pb ~ 1.15) compared to deeper soil horizons, with lithogenic Pb signatures (206Pb/207Pb > 1.2). Isotopic composition of Cu differs on contaminated and uncontaminated sites and cultivated and non-cultivated sites. The δ65Cu in the studied soil horizon ranged between -0.373 ‰ and 0.561 ‰. The most pronounced variations occurred in contaminated non cultivated and non-irrigated soils (0.529 ‰). The contaminated top horizons are enriched in isotopically heavier Cu (tailing materials), and δ65Cu decreased with depth. Irrigated (cultivated) and contaminated soils exhibited heavier Cu in the surface horizons (originated from tailing dust δ65Cu = 0.260), decrease of δ65Cu in Bt horizons (biological uptake of light isotope by crop, and their incorporation in this horizons) and increase of δ65Cu in Bc horizons. The Bc horizons of cultivated and irrigated Phaeozems are enriched in Mn nodules (0.2 - 1.5 cm diameter, prevailing Mn phase pyrochroite Mn(OH)2) which

  18. The Use of Lead Isotope and Rare Earth Element Geochemistry for Forensic Geographic Provenancing

    Science.gov (United States)

    Carey, A.; Darrah, T.; Harrold, Z.; Prutsman-Pfeiffer, J.; Poreda, R.

    2008-12-01

    Lead isotope and rare earth element composition of modern human bones are analyzed to explore their utility for geographical provenancing. DNA analysis is the standard for identification of individuals. DNA analysis requires a DNA match for comparison. Thus, DNA analysis is of limited use in cases involving unknown remains. Trace elements are incorporated into bones and teeth during biomineralization, recording the characteristics of an individual's geochemical environment. Teeth form during adolescence, recording the geochemical environment of an individual's youth. Bones remodel throughout an individual's lifetime. Bones consist of two types of bone tissue (cortical and trabecular) that remodel at different rates, recording the geochemical environment at the time of biomineralization. Cortical bone tissue, forming the outer surface of bones, is dense, hard tissue that remodels in 25-30 yrs. Conversely, trabecular bone tissue, the inner cavity of bones, is low density, porous and remodels in 2-5 years. Thus, analyzing teeth and both bone tissues allows for the development of a geographical time line capable of tracking immigration patterns through time instead of only an individual's youth. Geochemical isotopic techniques (Sr, O, C, N) have been used for geographical provenancing in physical anthropology. The isotopic values of Sr, C, O, N are predominantly a function of soil compositions in areas where food is grown or water is consumed. Application of these provenancing techniques has become difficult as an individual's diet may reflect the isotopic composition of foods obtained at the local grocer as opposed to local soil compositions. Thus, we explore the use of REEs and Pb isotopes for geographical provenancing. Pb and REEs are likely more reliable indicators of modern geographical location as their composition are high in bio-available sources such as local soils, atmospheric aerosols, and dust as opposed to Sr, C, O, N that are controlled by food and

  19. Ancient bronze coins from Mediterranean basin: LAMQS potentiality for lead isotopes comparative analysis with former mineral

    Science.gov (United States)

    Torrisi, L.; Italiano, A.; Torrisi, A.

    2016-11-01

    Bronze coins coming from the area of the Mediterranean basin, dated back the II-X Cent. A.D., were analyzed using different physical analytical techniques. Characteristic X-ray fluorescence was used with electrons and photons, in order to investigate the elemental composition of both the surface layers and bulk. Moreover, the quadrupole mass spectrometry coupled to laser ablation (LAMQS technique) in high vacuum was used to analyse typical material compounds from surface contamination. Mass spectrometry, at high resolution and sensitivity, extended up to 300 amu, allowed measuring the 208Pb/206Pb and 207Pb/206Pb isotopic ratios into the coins. Quantitative relative analyses of these isotopic ratios identify the coin composition such as a "fingerprint" depending on the mineral used to extract the lead. Isotopic ratios in coins can be compared to those of the possible minerals used to produce the bronze alloy. A comparison between the measured isotope ratios in the analyzed coins and the literature database, related to the mineral containing Pb as a function of its geological and geophysical extraction mine, is presented. The analysis, restricted to old coins and the mines of the Mediterranean basin, indicates a possible correlation between the coin compositions and the possible geological sites of the extracted mineral.

  20. Rapid and Sensitive Quantification of Isotopic Mixtures Using a Rapidly-Swept External Cavity Quantum Cascade Laser

    Energy Technology Data Exchange (ETDEWEB)

    Brumfield, Brian E.; Taubman, Matthew S.; Phillips, Mark C.

    2016-05-23

    A rapidly-swept external-cavity quantum cascade laser with an open-path Herriott cell is used to quantify gas-phase chemical mixtures of D2O and HDO at an update rate of 40 Hz (25 ms measurement time). The chemical mixtures were generated by evaporating D2O liquid near the open-path Herriott cell, allowing the H/D exchange reaction with ambient H2O to produce HDO. Fluctuations in the ratio of D2O and HDO on timescales of < 1 s due to the combined effects of plume transport and the H/D exchange chemical reaction are observed. Noise equivalent concentrations (1σ) (NEC) of 147.0 ppbv and 151.6 ppbv in a 25 ms measurement time are estimated for D2O and HDO respectively with a 127 m optical path. These NECs are reduced to 23.0 and 24.0 ppbv with a 1 s averaging time for D2O and HDO respectively. NECs < 200 ppbv are also estimated for N2O, F134A, CH4, Acetone, and SO2 for a 25 ms measurement time. Based on the NECs obtained for D2O and HDO, the isotopic precision for measurement of the [D2O]/[HDO] concentration ratio was studied. An isotopic precision of 33‰ and 5‰ was calculated for the current experimental conditions for measurement times of 25 ms and 1 s, respectively.

  1. Re-evaluation of lead isotopic data, southern Massif Central, France

    Science.gov (United States)

    Sinclair, A. J.; Macquar, J. C.; Rouvier, H.

    1993-04-01

    Three independent Pb isotope homogenizing processes operating on large volumes of rock material during limited intervals in the Phanerozoic have been used to define a unique evolutionary curve for rock and ore lead isotopic compositions of the southern Massif Central, France. The model is 126_2004_Article_BF00196336_TeX2GIFE1.gif begin{gathered}{text{ x}}_{text{t}} = 18.641{text{ }} - {text{ 9}}{text{.56(e}}^{{text{L1*t}}} - 1{text{)}} {text{y}}_{text{t}} = 15.678{text{ }} - {text{ 0}}{text{.06934(e}}^{{text{L2*t}}} - 1{text{)}} {text{ z}}_{text{t}} = 38.701{text{ }} - {text{ 30}}{text{.8(e}}^{{text{L3*t}}} - 1{text{)}} where xt, yt and zt are the calculated isotopic ratios (206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb respectively) at time t years ago and L1, L2 and L3 are the decay constants of 238U, 235U and 232Th respectively. The model gives the following ages for averages of the three sets of data used in its generation: age of mineralization for carbonate-hosted lead-zinc ore of Les Malines, ca. 150 Ma; emplacement of the Saint-Guiral-Liron granite, ca. 290 Ma; and an estimated average age of a group of Cambrian syngenetic deposits, ca. 520 Ma. These ages are in close agreement with ages determined by independent methods.

  2. Lead Isotopes and Temporal Records of Atmospheric Aerosol and Pollutants in Lichens

    Science.gov (United States)

    Getty, S. R.; Nash, T.; Asmerom, Y.

    2001-05-01

    Lichens are useful receptors of atmospheric particulate matter (PM) and pollutants due to their retention of body parts (unlike plants), slow growth rates, fairly uniform morphologies, lack of a vascular system, and sessile character over decades to centuries. Lichen biomonitoring has been used widely to map patterns of aerosol deposition, yet few studies have tested whether lichens can preserve a temporal record of airborne PM and pollutants. We show with U-Pb data that epilithic lichens (rock as host) can retain in their porous structure an integrated, decadal-scale history of changing aerosol inputs to desert ecosystems. Three lichens resided along an 80-km transect from a copper smelter (Douglas, AZ) closed in early 1987, to the ENE into adjacent New Mexico. For the radially growing lichen (Xanthoparmelia sp.), U-Pb data were obtained along cm-scale transects in the growth direction on a single thallus. Profiles from lichen rim to interior show increasing [Pb] and [U], or net accumulation with thallus age. Total lead contents are highest near the smelter. In contrast, each lead isotope profile (206Pb/207Pb) is flat during smelter operation, showing low ratios near the smelter (1.152) and high ratios (1.175) 80 km away. This suggests comparable mixtures of crust and smelter lead per locality over decades. Since smelter closure, lichens 80 km from the smelter show a sharp upturn in lead ratio in the recently grown lichen rim, indicating that smelter lead is either dispersed by aeolian recycling, or suppressed in desert soils. The amplitude and position of the isotope signal suggests a soil recovery "half-life" of about 13 yrs, a radial growth rate of 0.57+/-0.1 mm/yr, and a total lichen age of 105+/-18 yrs. Lichens near the smelter have no upturn in isotope ratio, indicating continued aeolian recylcing of lead from soils about 11 yrs after closure. Results at a far-removed desert site (c. New Mexico) also argue that isotope profiles reflect aerosol deposition

  3. Rapid Determination of Plutonium Isotopes in Environmental Samples Using Sequential Injection Extraction Chromatography and Detection by Inductively Coupled Plasma Mass Spectrometry

    DEFF Research Database (Denmark)

    Qiao, Jixin; Hou, Xiaolin; Roos, Per

    2009-01-01

    by detection of isolated analytes with inductively coupled plasma mass spectrometry (ICP-MS). The method has been devised for the determination of Pu isotopes at environmentally relevant concentrations, whereby it has been successfully applied to the analyses of large volumes/amounts of samples, for example......This article presents an automated method for the rapid determination of 239Pu and 240Pu in various environmental samples. The analytical method involves the in-line separation of Pu isotopes using extraction chromatography (TEVA) implemented in a sequential injection (SI) network followed....... The analytical results of Pu isotopes in the reference materials showed good agreement with the certified or reference values at the 0.05 significance level. Chemical yields of Pu ranged from 80 to 105%, and the decontamination factors for uranium, thorium, mercury and lead were all above 104. The duration...

  4. Authenticity of Benin metalworks evaluated by inductively coupled plasma mass spectrometry and lead isotope analyses

    Science.gov (United States)

    Fabbri, E.; Soffritti, C.; Merlin, M.; Vaccaro, C.; Garagnani, G. L.

    2017-05-01

    Two metal plaques and a cock statuette belonging to a private collection and stylistically consistent with the Royal Art of Benin (Nigeria) were investigated in order to verify their authenticity. The characterization of alloys and patinas were carried out by inductively coupled plasma mass spectrometry, optical microscopy, scanning electron microscopy and energy dispersion spectroscopy, and X-Ray diffraction spectrometry. Furthermore, thermal ionization mass spectrometry was used to assess the abundances of lead isotopes and to attempt a dating by the measurement of 210Pb/204Pb ratio. The results showed that all three artefacts were mainly composed of low lead-brass alloys, with relatively high concentrations of zinc, antimony, cadmium and aluminum in the solid copper solution. Microstructures were mostly dendritic, typical of as-cast brasses, and characterized by recrystallized non-homogeneous twinned grains in areas corresponding to surface decorations, probably due to multiple hammering steps followed by partial annealing treatments. The matrix was composed of a cored α-Cu solid solution together with non-metallic inclusions, lead globules and Sn-rich precipitates in interdendritic spaces. On the surface of all metalworks, both copper and zinc oxides, a non-continuous layer of sulphur-containing contaminants and chloride-containing compounds, were identified. The lead isotope results were consistent with brasses produced shortly before or after 1900 CE. Overall, the data obtained by different techniques supported the hypothesis that the three artefacts were not authentic.

  5. Potential of Opuntia ficus-indica for air pollution biomonitoring: a lead isotopic study.

    Science.gov (United States)

    El Hayek, Eliane; El Samrani, Antoine; Lartiges, Bruno; Kazpard, Veronique; Benoit, Mathieu; Munoz, Marguerite

    2015-11-01

    Opuntia ficus-indica (Ofi) is a long-domesticated cactus that is widespread throughout arid and semiarid regions. Ofi is grown for both its fruits and edible cladodes, which are flattened photosynthetic stems. Young cladodes develop from mother cladodes, thus forming series of cladodes of different ages. Therefore, successive cladodes may hold some potential for biomonitoring over several years the local atmospheric pollution. In this study, cladodes, roots, dust deposited onto the cladodes, and soil samples were collected in the vicinity of three heavily polluted sites, i.e., a fertilizer industry, the road side of a highway, and mine tailings. The lead content was analyzed using atomic absorption spectroscopy (AAS) and inductively coupled plasma-mass spectrometry (ICP-MS). Scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDX) was used to characterize the cladode surfaces and the nature of dust deposit, and the lead isotopes were analyzed to identify the origin of Pb. The results show that (i) Ofi readily bioaccumulates Pb, (ii) the lead isotopic composition of cladodes evidences a foliar pathway of lead into Ofi and identifies the relative contributions of local Pb sources, and (iii) an evolution of air quality is recorded with successive cladodes, which makes Ofi a potential biomonitor to be used in environmental and health studies.

  6. Tracing geogenic and anthropogenic sources in urban dusts: Insights from lead isotopes

    Science.gov (United States)

    Del Rio-Salas, R.; Ruiz, J.; De la O-Villanueva, M.; Valencia-Moreno, M.; Moreno-Rodríguez, V.; Gómez-Alvarez, A.; Grijalva, T.; Mendivil, H.; Paz-Moreno, F.; Meza-Figueroa, D.

    2012-12-01

    Tracing the source of metals in the environment is critical to understanding their pollution level and fate. Geologic materials are an important source of airborne particulate matter, but the contribution of contaminated soil to concentrations of Pb in airborne dust is not yet widely documented. To examine the potential significance of this mechanism, surface soil samples were collected, as well as wind-transported dust trapped at 1 and 2 m height at seven different locations including residential, industrial, high-traffic and rural sites. Samples of dust deposited on roofs from 24 schools were also obtained and analyzed for Pb isotope ratios. Spatial distribution of Pb of airborne and sedimented dust suggests a process dominated by re-suspension/sedimentation, which was controlled by erosion, traffic and topography of the urban area. Anthropogenic lead input in the city grades outward the urban zone toward geogenic values. Our results shows that Pb-isotopic signatures of leaded gasoline are imprinted in dust sedimented on roofs. Considering that leaded-gasoline has not been in use in Mexico since two decades ago, this signature shows not only a Pb-legacy in soil, but also a re-suspension process affecting air column below 3 m in height. The combination of the 207Pb/206Pb data of the surrounding rocks and urban dust, reveal three well-defined zones with remarkable anthropogenic influence, which correspond to the oldest urban sectors. This work highlights the importance of spatial characterization of metals in particles suspended below a height of 3 m of the airborne column, a fact that should be considered to identify exposure paths to humans and the potential risks. Lead isotope signatures allowed the identification of geogenic and anthropogenic emission sources for dust, a matter that deserves consideration in the efforts to control airborne metal emissions.

  7. Lead isotopes and trace metal ratios of aerosols as tracers of Pb pollution sources in Kanpur, India

    Science.gov (United States)

    Sen, Indra; Bizimis, Michael; Tripathi, Sachchida; Paul, Debajyoti; Tyagi, Swati; Sengupta, Deep

    2015-04-01

    The anthropogenic flux of Pb in the Earth's surface is almost an order of magnitude higher than its corresponding natural flux [1]. Identifying the sources and pathways of anthropogenic Pb in environment is important because Pb toxicity is known to have adverse effects on human health. Pb pollution sources for America, Europe, and China are well documented. However, sources of atmospheric Pb are unknown in India, particularly after leaded gasoline was phased out in 2000. India has a developing economy with a rapidly emerging automobile and high temperature industry, and anthropogenic Pb emission is expected to rise in the next decade. In this study, we report on the Pb- isotope compositions and trace metal ratios of airborne particulates collected in Kanpur, an industrial city in northern India. The Pb concentration in the airborne particulate matter varies between 14-216 ng/m3, while the other heavy metals vary by factor of 10 or less, e.g. Cd=0.3-3 ng/m3, As=0.4-3.5 ng/m3, Zn=36-161 ng/m3, and Cu=3-22 ng/m3. The 206Pb/207Pb, 208Pb/206Pb, and 208Pb/207Pb vary between 1.112 - 1.129, 2.123-2.141, and 2.409-2.424 respectively, and are highly correlated with each other (R2>0.9). Pb isotopes and trace metal data reveals that coal combustion is the major source of anthropogenic Pb in the atmosphere, with limited contribution from mining and smelting processes. We further conclude that combination of Pb isotope ratios and V/Pb ratios are powerful tracers for Pb source apportionment studies, which is otherwise difficult to differentiate based only on Pb systematics [1] Sen and Peucker-Ehrenbrink (2012), Environ. Sci. Technol.(46), 8601-8609

  8. Rapid collection of iron hydroxide for determination of Th isotopes in seawater.

    Science.gov (United States)

    Okubo, Ayako; Obata, Hajime; Magara, Masaaki; Kimura, Takaumi; Ogawa, Hiroshi

    2013-12-04

    This work introduces a novel method of recovery of iron hydroxide using a DIAION CR-20 chelating resin column to determine Th isotopes in seawater with a sector field (SF) inductively coupled plasma mass spectrometer (ICP-MS). Thorium isotopes in seawater were co-precipitated with iron hydroxide, and this precipitate was sent to chelating resin column. Ferric ions in the iron hydroxide were bonded to functional groups of the chelating resin directly, resulting in a pH increase of the effluent by release of hydroxide ion from the iron hydroxide. The co-precipitated thorium isotopes were quantitatively collected within the column, which indicated that thorium was retained on the iron hydroxide remaining on the chelating column. The chelating column quantitatively collected (232)Th with iron hydroxide in seawater at flow rates of 20-25 mL min(-1). Based on this flow rate, a 5 L sample was processed within 3-4 h. The >20 h aging of iron hydroxide tends to reduce the recovery of (232)Th. The rapid collection method was successfully applied to the determination of (230)Th and (232)Th in open-ocean seawater samples. Copyright © 2013 Elsevier B.V. All rights reserved.

  9. A rapid method for the sampling of atmospheric water vapour for isotopic analysis.

    Science.gov (United States)

    Peters, Leon I; Yakir, Dan

    2010-01-01

    Analysis of the stable isotopic composition of atmospheric moisture is widely applied in the environmental sciences. Traditional methods for obtaining isotopic compositional data from ambient moisture have required complicated sampling procedures, expensive and sophisticated distillation lines, hazardous consumables, and lengthy treatments prior to analysis. Newer laser-based techniques are expensive and usually not suitable for large-scale field campaigns, especially in cases where access to mains power is not feasible or high spatial coverage is required. Here we outline the construction and usage of a novel vapour-sampling system based on a battery-operated Stirling cycle cooler, which is simple to operate, does not require any consumables, or post-collection distillation, and is light-weight and highly portable. We demonstrate the ability of this system to reproduce delta(18)O isotopic compositions of ambient water vapour, with samples taken simultaneously by a traditional cryogenic collection technique. Samples were collected over 1 h directly into autosampler vials and were analysed by mass spectrometry after pyrolysis of 1 microL aliquots to CO. This yielded an average error of system provides a rapid and reliable alternative to conventional cryogenic techniques, particularly in cases requiring high sample throughput or where access to distillation lines, slurry maintenance or mains power is not feasible.

  10. Using trace element content and lead isotopic composition to assess sources of PM in Tijuana, Mexico

    Science.gov (United States)

    Salcedo, D.; Castro, T.; Bernal, J. P.; Almanza-Veloz, V.; Zavala, M.; González-Castillo, E.; Saavedra, M. I.; Perez-Arvízu, O.; Díaz-Trujillo, G. C.; Molina, L. T.

    2016-05-01

    PM2.5 samples were collected at two urban sites (Parque Morelos (PQM) and CECyTE (CEC)) in Tijuana during the Cal-Mex campaign from May 24 to June 5, 2010. Concentration of trace elements (Mg, Al, Ti, V, Mn, Fe, Co, Ni, Zn, Cu, Ga, As, Se, Rb, Sr, Mo, Cd, Sn, Sb, Ba, La, Ce, and Pb), and Pb isotopic composition were determined in order to study the sources of PM impacting each site. Other chemical analysis (gravimetric, elemental and organic carbon (EC/OC), and polycyclic aromatic hydrocarbons (PAHs)), were also performed. Finally, back-trajectories were calculated to facilitate the interpretation of the chemical data. Trace elements results show that CEC is a receptor site affected by mixed regional sources: sea salt, mineral, urban, and industrial. On the other hand, PQM seems to be impacted mainly by local sources. In particular, Pb at CEC is of anthropogenic, as well as crustal origin. This conclusion is supported by the lead isotopic composition, whose values are consistent with a combination of lead extracted from US mines, and lead from bedrocks in the Mexican Sierras. Some of the time variability observed can be explained using the back-trajectories.

  11. GCM Analysis of the collective properties of lead isotopes with exact projection on particle numbers

    CERN Document Server

    Heenen, P H; Bender, M; Bonche, P; Flocard, Hubert

    2001-01-01

    We present a microscopic analysis of the collective behaviour of the lead isotopes in the vicinity of Pb208. In this study, we rely on a coherent approach based on the Generator Coordinate Method including exact projection on N and Z numbers within a collective space generated by means of the constrained Hartree-Fock BCS method. With the same Hamiltonian used in HF+BCS calculations, we have performed a comprehensive study including monopole, quadrupole and octupole excitations as well as pairing vibrations. We find that, for the considered nuclei, the collective modes which modify the most the conclusions drawn from the mean-field theory are the octupole and pairing vibrations.

  12. Lead isotopic evidence for evolutionary changes in magma-crust interaction, Central Andes, southern Peru

    Science.gov (United States)

    Barreiro, Barbara A.; Clark, Alan H.

    1984-07-01

    Lead isotopic measurements were made on Andean igneous rocks of Jurassic to Recent age in Moquegua and Tacna Departments, southernmost Peru, to clarify the petrogenesis of the rocks and, in particular, to investigate the effect of crustal thickness on rock composition. This location in the Cordillera Occidental is ideal for such a study because the ca. 2 Ga Precambrian basement rocks (Arequipa massif) have a distinct Pb isotopic signature which is an excellent tracer of crustal interaction, and because geomorphological research has shown that the continental crust was here thickened drastically in the later Tertiary. Seven samples of quartz diorites and granodiorites from the Ilo and Toquepala intrusive complexes, and seven samples of Toquepala Group subaerial volcanics were analyzed for Pb isotopic compositions. The plutonic rocks range in age from Jurassic to Eocene; the volcanic rocks are all Late Cretaceous to Eocene. With one exception, the Pb isotopic ratios are in the ranges 206Pb/ 204Pb= 18.52-18.75, 207Pb/ 204Pb= 15.58-15.65, and 208Pb/ 204Pb= 38.53-38.74. The data reflect very little or no interaction with old continental material of the Arequipa massif type. Lead from four Miocene Huaylillas Formation ash-flow tuffs, two Pliocene Capillune Formation andesites and five Quaternary Barroso Group andesites has lower 206Pb/ 204Pb than that in the pre-Miocene rocks, but relatively high 207Pb/ 204Pb and 208Pb/ 204Pb ( 206Pb/ 204Pb= 18.16-18.30, 207Pb/ 204Pb= 15.55-15.63, 208Pb/ 204Pb= 38.45-38.90). Tilton and Barreiro [9] have shown that contamination by Arequipa massif granulites can explain the isotopic composition of the Barosso Group lavas, and the new data demonstrate that this effect is evident, to varying degrees, in all the analysed Neogene volcanic rocks. The initial incorporation of such basement material into the magma coincided with the Early Miocene uplift of this segment of the Cordillera Occidental [32], and thus with the creation of a thick

  13. Rapid acceleration leads to rapid weakening in earthquake-like laboratory experiments

    Science.gov (United States)

    Chang, Jefferson C.; Lockner, David A.; Reches, Z.

    2012-01-01

    After nucleation, a large earthquake propagates as an expanding rupture front along a fault. This front activates countless fault patches that slip by consuming energy stored in Earth’s crust. We simulated the slip of a fault patch by rapidly loading an experimental fault with energy stored in a spinning flywheel. The spontaneous evolution of strength, acceleration, and velocity indicates that our experiments are proxies of fault-patch behavior during earthquakes of moment magnitude (Mw) = 4 to 8. We show that seismically determined earthquake parameters (e.g., displacement, velocity, magnitude, or fracture energy) can be used to estimate the intensity of the energy release during an earthquake. Our experiments further indicate that high acceleration imposed by the earthquake’s rupture front quickens dynamic weakening by intense wear of the fault zone.

  14. Rapid chelometric determination of lead in lubricating oils via mercaptoacetate extraction.

    Science.gov (United States)

    Banerjee, S; Dutta, R K

    1973-01-01

    A rapid complexometric method for the estimation of lead in lubricating oil has been developed. The lead naphthenate present in the oil is extracted with a mixture of dilute thioglycollic acid and nitric acid. The aqueous extract containing lead mercaptoacetate is titrated with EDTA at pH 5 with Xylenol Orange as indicator. The lead content can be determined within 15-20 min.

  15. Formation of black and white smokers in the North Fiji Basin: Sulfur and lead isotope constraints

    Science.gov (United States)

    Kim, J.; Lee, I.; Lee, K.; Yoo, C.; Ko, Y.

    2004-12-01

    The hydrothermal chimneys were recovered from 16o50¡_S triple junction area in the North Fiji Basin. The chimney samples are divided into three groups according to their mineralogy and metal contents; 1) Black smoker, 2) White smoker, 3) Transitional type. Black smoker chimneys are mainly composed of chalcopyrite and pyrite, and are enriched in high temperature elements such as Cu, Co, Mo, and Se. White smoker chimneys consist of sphalerite and marcasite with trace of pyrite and chalcopyrite, and are enriched in low temperature elements (Zn, Cd, Pb, As, and Ga). Transitional chimneys show intermediate characteristics in mineralogy and composition between black and white smokers. Basaltic rocks sampled from the triple junction show wide variation in geochemistry. Trace elements composition of basaltic rocks indicates that the magma genesis in the triple junction area was affected by mixing between N-MORB and E-MORB sources. The sulfur and lead isotope compositions of hydrothermal chimneys show distinct differences between the black and white smokers. Black smokers are depleted in 34S (Øä34S = +0.4 to +4.8) and are low in lead isotope composition (206Pb/204Pb = 18.082 to 18.132; 207Pb/204Pb = 15.440 to 15.481; 208Pb/204Pb = 37.764 to 37.916) compared to white smoker and transitional chimneys (Øä34S = +2.4 to +5.6; 206Pb/204Pb = 18.122 to 18.193; 207Pb/204Pb = 15.475 to 15.554; 208Pb/204Pb = 37.882 to 38.150). The heavier sulfur isotopic fractionation in white smoker can be explained by boiling of hydrothermal fluids and mixing with ambient seawater. The lead isotope compositions of the hydrothermal chimneys indicate that the metal in black and white smokers come from hydrothermal reaction with N-MORB and E-MORB, respectively. Regarding both black and white smoker are located in the same site, the condition of phase separation of hydrothermal fluid that formed white smokers might result from P-T condition of high temperature reaction zone below the hydrothermal

  16. Lead isotopic composition and lead source of the Tongchanghe basalt-type native copper-chalcocite deposit in Ninglang, western Yunnan, China

    Institute of Scientific and Technical Information of China (English)

    ZHANG Qian; ZHU Xiaoqing; ZHANG Zhengwei

    2006-01-01

    The Tongchanghe native copper-chalcocite deposit at Ninglang occurs in low-Ti basalts of western Yunnan, and the mode of fault-filling & metasomatism metallogenesis indicates that this deposit is of late-stage hydrothermal origin. This makes it more complicated to define the source of ore-forming materials. This paper introduces the Pb isotope data of Himalayan alkali-rich porphyries, regional Early-Middle Proterozoic metamorphic rock basement and various types of rocks of the mining district in western Yunnan with an attempt to constrain the origin of the Tongchanghe native copper-chalcocite deposit at Ninglang.The results showed that the ores are relatively homogeneous in Pb isotopic composition, implying a simple ore-forming material source. The three sets of Pb isotopic ratios in the Himalayan alkali-rich porphyries are all higher than those of the ores; the regional basement metamorphic rocks show a wide range of variations in Pb isotopic ratio, quite different from the isotopic composition of ore lead; the Pb isotopic composition of the Triassic sedimentary rocks and mudstone and siltstone interbeds in the Late Permian Heinishao Formation (corresponding to the forth cycle of basaltic eruption) in the mining district has the characteristics of radiogenic lead and is significantly different from the isotopic composition of ore lead; like the ores, the Emeishan basalts in the mining district and those regionally distributed possess the same Pb isotopic composition, showing a complete overlap with respect to their distribution range. From the above, the possibilities can be ruled out that the ore-forming materials of the Tongchanghe deposit were derived from the basement, a variety of Himalayan magmatic activities, etc. It is thereby defined that the ore-forming materials were derived largely from the Emeishan basalts. From the data available it is deduced that the native cupper-chalcocite-type metallogenesis that occurred in the Emeishan basalt-distributed area

  17. Holocene elemental, lead isotope and charcoal record from peat in southern Poland

    Directory of Open Access Journals (Sweden)

    K. Tudyka

    2017-03-01

    Full Text Available This article presents a mid-resolution elemental, isotopic and charcoal record from 10700 BC to AD 500 in a peat core located in Żyglin (southern Poland. The objective is to give insight into the proxies with emphasis on lead (Pb sources in this minerogenic peat deposit. During the Early Holocene (10700–7550 BC the average 206Pb/207Pb quotient was around 1.196. This isotopic signature is consistent with natural dust derived from long-distance soil and rock weathering. The Mid-Holocene period (7550–3200 BC shows a significant change in the peat accumulation conditions. The growth rate is approximately 0.04 mm yr-1 and the 206Pb/207Pb quotients are shifted toward values that are found in local galena ores. This is simultaneous with a significantly increased lead flux which further confirms local sources of material in this peat deposit. In the Late Holocene period (3200 BC–AD 500 a large quantity of charcoal particles with diameters ranging from 2 mm up to 3 cm is found; also, Pb, Zn and Cu fluxes reach their highest values. This period corresponds to the Eneolithic, Bronze and Iron Ages, and human impact is recorded as charcoal.

  18. {ital E}3 transition probabilities in the platinum, mercury, and lead isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Egido, J.L.; Martin, V.; Robledo, L.M.; Sun, Y. [Departamento de Fisica Teorica C-XI, Universidad Autonoma de Madrid, E-28049 Madrid (Spain)]|[Analisis Numerico, Facultad de Informatica, Universidad Politecnica de Madrid, E-28660 Madrid (Spain)]|[Department of Physics and Atmospheric Science, Drexel University, Philadelphia, Pennsylvania 19104 (United States)]|[Joint Institute for Heavy Ion Research, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 (United States)

    1996-06-01

    Spectroscopical properties of the platinum, mercury, and lead isotopes are studied within the Hartree-Fock plus BCS framework with the finite range density-dependent Gogny force. These properties are also studied beyond mean-field theory by combining the use of generator-coordinate-method-like wave functions with the angular momentum projection technique as to generate many-body correlated wave functions that are at the same time eigenstates of the angular momentum operator. We apply this formalism to the calculation of reduced transition probabilities {ital B}({ital E}3) from the lowest-lying octupole collective state to the ground state of several isotopes of the platinum, mercury, and lead nuclei whose experimental {ital B}({ital E}3) values present a peculiar behavior. The projected calculations show a large improvement over the unprojected ones when compared with the experimental data. The unprojected calculations are unable to predict any structure in the {ital B}({ital E}3). {copyright} {ital 1996 The American Physical Society.}

  19. Comparison of lead isotopes with source apportionment models, including SOM, for air particulates.

    Science.gov (United States)

    Gulson, Brian; Korsch, Michael; Dickson, Bruce; Cohen, David; Mizon, Karen; Davis, J Michael

    2007-08-01

    We have measured high precision lead isotopes in PM(2.5) particulates from a highly-trafficked site (Mascot) and rural site (Richmond) in the Sydney Basin, New South Wales, Australia to compare with isotopic data from total suspended particulates (TSP) from other sites in the Sydney Basin and evaluate relationships with source fingerprints obtained from multi-element PM(2.5) data. The isotopic data for the period 1998 to 2004 show seasonal peaks and troughs that are more pronounced in the rural site for the PM(2.5).samples but are consistent with the TSP. The Self Organising Map (SOM) method has been applied to the multi-element PM(2.5) data to evaluate its use in obtaining fingerprints for comparison with standard statistical procedures (ANSTO model). As seasonal effects are also significant for the multi-element data, the SOM modelling is reported as site and season dependent. At the Mascot site, the ANSTO model exhibits decreasing (206)Pb/(204)Pb ratios with increasing contributions of fingerprints for "secondary smoke" (industry), "soil", "smoke" and "seaspray". Similar patterns were shown by SOM winter fingerprints for both sites. At the rural site, there are large isotopic variations but for the majority of samples these are not associated with increased contributions from the main sources with the ANSTO model. For two winter sampling times, there are increased contributions from "secondary industry", "smoke", "soil" and seaspray with one time having a source or sources of Pb similar to that of Mascot. The only positive relationship between increasing (206)Pb/(204)Pb ratio and source contributions is found at the rural site using the SOM summer fingerprints, both of which show a significant contribution from sulphur. Several of the fingerprints using either model have significant contributions from black carbon (BC) and/or sulphur (S) that probably derive from diesel fuels and industrial sources. Increased contributions from sources with the SOM summer

  20. Impact on the environment from steel bridge paint deterioration using lead isotopic tracing, paint compositions and soil deconstruction.

    Science.gov (United States)

    Gulson, Brian; Chiaradia, Massimo; Davis, Jeffrey; O'Connor, Gary

    2016-04-15

    Deterioration and repair of lead paint on steel structures can result in contamination of the ambient environment but other sources of lead such as from past use of leaded paint and gasoline and industrial activities can also contribute to the contamination. Using a combination of high precision lead isotopic tracing, detailed paint examination, including with scanning electron microscopy, and soil deconstruction we have compared paint on a steel bridge and bulk soil and lead-rich particles separated from soil. The majority of Pb found in the paint derives from Australian sources but some also has a probable US origin. The isotopic data for the bulk soils and selected particles lie on a mixing line with end members the geologically ancient Broken Hill lead and possible European lead which is suggested to be derived from old lead paint and industrial activities. Data for gasoline-derived particulates lie on this array and probably contribute to soil Pb. Although paint from the bridge can be a source of lead in the soils, isotopic tracing, paint morphology and mineralogical identification indicate that other sources, including from paint, gasoline and industrial activities, are contributing factors to the lead burden. Even though physical characteristics and elemental composition are the same in some particles, the isotopic signatures demonstrate that the sources are different. Plots using (206)Pb/(208)Pb vs (206)Pb/(207)Pb ratios, the common representation these days, do not allow for source discrimination in this investigation.

  1. Lead concentrations and isotope ratios in street dust determined by electrothermal atomic absorption spectrometry and inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Nageotte, S M; Day, J P

    1998-01-01

    A major source of environmental lead, particularly in urban areas, has been from the combustion of leaded petrol. Street dust has previously been used to assess urban lead contamination, and the dust itself can also be a potential source of lead ingestion, particularly to children. The progressive reduction of lead in petrol, in recent years, would be expected to have been reflected in a reduction of lead in urban dust. We have tested this hypothesis by repeating an earlier survey of Manchester street dust and carrying out a comparable survey in Paris. Samples were collected from streets and parks, lead was extracted by digestion with concentrated nitric acid and determined by electrothermal atomic absorption spectrometry. Lead isotope ratios were measured by inductively coupled plasma mass spectrometry. Results for Manchester show that lead concentrations have fallen by about 40% (street dust averages, 941 micrograms g-1 (ppm) in 1975 down to 569 ppm in 1997). In Paris, the lead levels in street dust are much higher and significant differences were observed between types of street (not seen in Manchester). Additionally, lead levels in parks were much lower than in Manchester. Samples collected under the Eiffel Tower had very high concentrations and lead isotope ratios showed that this was unlikely to be fallout from motor vehicles but could be due to the paint used on the tower. Isotope ratios measurements also revealed that lead additives used in France and the UK come from different sources.

  2. Lead Isotope Constraints on the Sources of Ore Metals in SW Mexican Deposits

    Science.gov (United States)

    Potra, A.; Macfarlane, A. W.

    2007-12-01

    Lead isotope ratios from mineral deposits in southern Mexico increase with distance from the trench from 206Pb/204Pb values between 18.597 and 18.650 in the coastal area to values between 18.712 and 19.069 approximately 800 km east from the trench. This variation has been attributed to increasing assimilation of radiogenic lead from the crust with increasing distance from the trench. New sampling was undertaken in this area to provide a clearer picture of the potential sources of ore metals in this arc system, and also, if possible, to examine whether ore metal sources differ among the proposed tectonostratigraphic exotic terranes of southern Mexico. New TIMS lead isotope analyses are presented for samples from the metamorphic basement rocks of the Guerrero Terrane, the Late Cretaceous clastic sedimentary rocks from the Upper Mesozoic Assemblage, and for mid-Cretaceous igneous rocks, as well as for samples from the Oligocene La Verde, Esmeralda, and El Malacate copper prospects. Whole rock samples of schist from the Jurassic-Cretaceous Arteaga Complex and phyllite and slate from the Tierra Caliente Complex contain radiogenic lead relative to bulk earth models, with 206Pb/204Pb ranging from 18.981-19.256. These values are substantially more radiogenic than published values of analyses of metagabbro and charnockite from the Grenvillian-age Oaxaca Terrane. Sedimentary rocks (sandstones, siltstones, and marls) belonging to the Huetamo Sequence have 206Pb/204Pb values ranging between 18.630 to 18.998, close to the published data for the sediments from IPOD-DSDP Sites 487 and 488, Cocos Plate. Whole rock analyses of igneous rocks (granodiorite) collected from La Verde and El Malacate have 206Pb/204Pb ranging from 18.764 to 18.989, clustering between the fields represented by the sedimentary and the metamorphic rocks, suggesting assimilation of lead from these components. Ore samples from La Verde and Esmeralda have 206Pb/204Pb between 18.685 and 18.731 and plot within

  3. A lead isotope study of mineralization in the Saudi Arabian Shield

    Science.gov (United States)

    Stacey, J.S.; Doe, B.R.; Roberts, R.J.; Delevaux, M.H.; Gramlich, J.W.

    1980-01-01

    New lead isotope data are presented for some late Precambrian and early Paleozoic vein and massive sulfide deposits in the Arabian Shield. Using the Stacey Kramers (1975) model for lead isotope evolution, isochron model ages range between 720 m.y. and 420 m.y. Most of the massive sulfide deposits in the region formed before 680 m.y. ago, during evolution of the shield. Vein type mineralization of higher lead content occurred during the Pan African event about 550 m.y. ago and continued through the Najd period of extensive faulting in the shield that ended about 530 m.y. ago. Late post-tectonic metamorphism may have been responsible for vein deposits that have model ages less than 500 m.y. Alternatively some of these younger model ages may be too low due to the mineralizing fluids acquiring radiogenic lead from appreciably older local crustal rocks at the time of ore formation. The low207Pb/204Pb ratios found for the deposits in the main part of the shield and for those in north-eastern Egypt, indicate that the Arabian craton was formed in an oceanic crustal environment during the late Precambrian. Involvement of older, upper-crustal material in the formation of the ore deposits in this part of the shield is precluded by their low207Pb/204Pb and208Pb/204Pb characteristics. In the eastern part of the shield, east of longitude 44??20???E towards the Al Amar-Idsas fault region, lead data are quite different. They exhibit a linear207Pb/204Pb-206Pb/204Pb relationship together with distinctly higher208Pb/204Pb characteristics. These data imply the existence of lower crustal rocks of early Proterozoic age that apparently have underthrust the shield rocks from the east. If most of the samples we have analyzed from this easterly region were mineralized 530 m.y. ago, then the age of the older continental rocks is 2,100??300 m.y. (2??). The presence of upper crustal rocks, possibly also of early Proterozoic age, is indicated by galena data from Hailan in South Yemen and also

  4. Impact of historical mining assessed in soils by kinetic extraction and lead isotopic ratios

    Energy Technology Data Exchange (ETDEWEB)

    Camizuli, E., E-mail: estelle.camizuli@u-bourgogne.fr [UMR 6298, ArTeHiS, Université de Bourgogne — CNRS — Culture, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France); Monna, F. [UMR 6298, ArTeHiS, Université de Bourgogne — CNRS — Culture, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France); Bermond, A.; Manouchehri, N.; Besançon, S. [Institut des sciences et industries du vivant et de l' environnement (AgroParisTech), Laboratoire de Chimie Analytique, 16, rue Claude Bernard, 75231 Paris Cedex 05 (France); Losno, R. [UMR 7583, LISA, Universités Paris 7-Paris 12 — CNRS, 61 av. du Gal de Gaulle, 94010 Créteil Cedex (France); Oort, F. van [UR 251, Pessac, Institut National de la Recherche Agronomique, Centre de Versailles-Grignon, RD 10, 78026 Versailles Cedex (France); Labanowski, J. [UMR 7285, IC2MP, Université de Poitiers — CNRS, 4, rue Michel Brunet, 86022 Poitiers (France); Perreira, A. [UMR 6298, ArTeHiS, Université de Bourgogne — CNRS — Culture, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France); Chateau, C. [UFR SVTE, Université de Bourgogne, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France); Alibert, P. [UMR 6282, Biogeosciences, Université de Bourgogne — CNRS, 6 bd Gabriel, Bat. Gabriel, 21000 Dijon (France)

    2014-02-01

    The aim of this study is to estimate the long-term behaviour of trace metals, in two soils differently impacted by past mining. Topsoils from two 1 km{sup 2} zones in the forested Morvan massif (France) were sampled to assess the spatial distribution of Cd, Cu, Pb and Zn. The first zone had been contaminated by historical mining. As expected, it exhibits higher trace-metal levels and greater spatial heterogeneity than the second non-contaminated zone, supposed to represent the local background. One soil profile from each zone was investigated in detail to estimate metal behaviour, and hence, bioavailability. Kinetic extractions were performed using EDTA on three samples: the A horizon from both soil profiles and the B horizon from the contaminated soil. For all three samples, kinetic extractions can be modelled by two first-order reactions. Similar kinetic behaviour was observed for all metals, but more metal was extracted from the contaminated A horizon than from the B horizon. More surprising is the general predominance of the residual fraction over the “labile” and “less labile” pools. Past anthropogenic inputs may have percolated over time through the soil profiles because of acidic pH conditions. Stable organo-metallic complexes may also have been formed over time, reducing metal availability. These processes are not mutually exclusive. After kinetic extraction, the lead isotopic compositions of the samples exhibited different signatures, related to contamination history and intrinsic soil parameters. However, no variation in lead signature was observed during the extraction experiment, demonstrating that the “labile” and “less labile” lead pools do not differ in terms of origin. Even if trace metals resulting from past mining and metallurgy persist in soils long after these activities have ceased, kinetic extractions suggest that metals, at least for these particular forest soils, do not represent a threat for biota. - Highlights: • Trace

  5. Strange behavior of rapidity dependent strangeness enhancement of particles containing and not containing leading quarks

    Science.gov (United States)

    Dey, Kalyan; Bhattacharjee, B.

    2017-09-01

    Rapidity dependent strangeness enhancement factors for the identified particles have been studied with the help of a string based hadronic transport model UrQMD-3.3 (Ultra-relativistic Quantum Molecular Dynamics) at FAIR energies. A strong rapidity dependent strangeness enhancement could be observed with our generated data for Au + Au collisions at the beam energy of 30A GeV. The strangeness enhancement is found to be maximum at mid-rapidity for the particles containing leading quarks while for particles consisting of produced quarks only, the situation is seen to be otherwise. Such rapidity dependent strangeness enhancement could be traced back to the dependence of rapidity width on centrality or otherwise on the distribution of net-baryon density.

  6. Rapid directional solidification in Sn-Cu lead-free solder

    Institute of Scientific and Technical Information of China (English)

    Jun Shen; Yongchang Liu; Houxiu Gao

    2006-01-01

    An experimental study on the microstructures of a rapid directionally solidified metallo-eutectic Sn-Cu alloy was carried out.This material is an important alloy that is used as a lead-free solder. The results showed that the kinetic undercooling due to the rapid solidification process led to the formation of a pseudoeutectic zone, whereas the hypereutectic reaction produced the regular lamellar structure in the hypereutectic Sn-1.0Cu alloy. The corresponding arm spacing in the obtained lamellar phases decreased gradually with the increase of the applied cooling rate, which corresponded well with the prediction of a rapid directional solidification model.

  7. Rapid determination of plutonium isotopes in environmental samples using sequential injection extraction chromatography and detection by inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Qiao, Jixin; Hou, Xiaolin; Roos, Per; Miró, Manuel

    2009-10-01

    This article presents an automated method for the rapid determination of 239Pu and 240Pu in various environmental samples. The analytical method involves the in-line separation of Pu isotopes using extraction chromatography (TEVA) implemented in a sequential injection (SI) network followed by detection of isolated analytes with inductively coupled plasma mass spectrometry (ICP-MS). The method has been devised for the determination of Pu isotopes at environmentally relevant concentrations, whereby it has been successfully applied to the analyses of large volumes/amounts of samples, for example, 100-200 g of soil and sediment, 20 g of seaweed, and 200 L of seawater following analyte preconcentration. The investigation of the separation capability of the assembled SI system revealed that up to 200 g of soil or sediment can be treated using a column containing about 0.70 g of TEVA resin. The analytical results of Pu isotopes in the reference materials showed good agreement with the certified or reference values at the 0.05 significance level. Chemical yields of Pu ranged from 80 to 105%, and the decontamination factors for uranium, thorium, mercury and lead were all above 10(4). The duration of the in-line extraction chromatographic run was determination of Pu isotopes in environmental risk assessment and emergency preparedness scenarios.

  8. Isotopically constrained lead sources in fugitive dust from unsurfaced roads in the southeast Missouri mining district

    Science.gov (United States)

    Witt, Emitt C.; Pribil, Michael; Hogan, John P; Wronkiewicz, David

    2016-01-01

    The isotopic composition of lead (Pb) in fugitive dust suspended by a vehicle from 13 unsurfaced roads in Missouri was measured to identify the source of Pb within an established long-term mining area. A three end-member model using 207Pb/206Pb and concentration as tracers resulted in fugitive dust samples plotting in the mixing field of well characterized heterogeneous end members. End members selected for this investigation include the 207Pb/206Pb for 1) a Pb-mixture representing mine tailings, 2) aerosol Pb-impacted soils within close proximity to the Buick secondary recycling smelter, and 3) an average of soils, rock cores and drill cuttings representing the background conditions. Aqua regia total concentrations and 207Pb/206Pb of mining area dust suggest that 35.4–84.3% of the source Pb in dust is associated with the mine tailings mixture, 9.1–52.7% is associated with the smelter mixture, and 0–21.6% is associated with background materials. Isotope ratios varied minimally within the operational phases of sequential extraction suggesting that mixing of all three Pb mixtures occurs throughout. Labile forms of Pb were attributed to all three end members. The extractable carbonate phase had as much as 96.6% of the total concentration associated with mine tailings, 51.8% associated with smelter deposition, and 34.2% with background. The next most labile geochemical phase (Fe + Mn Oxides) showed similar results with as much as 85.3% associated with mine tailings, 56.8% associated with smelter deposition, and 4.2% associated with the background soil.

  9. Isotopically constrained lead sources in fugitive dust from unsurfaced roads in the southeast Missouri mining district.

    Science.gov (United States)

    Witt, Emitt C; Pribil, Michael J; Hogan, John P; Wronkiewicz, David J

    2016-09-01

    The isotopic composition of lead (Pb) in fugitive dust suspended by a vehicle from 13 unsurfaced roads in Missouri was measured to identify the source of Pb within an established long-term mining area. A three end-member model using (207)Pb/(206)Pb and concentration as tracers resulted in fugitive dust samples plotting in the mixing field of well characterized heterogeneous end members. End members selected for this investigation include the (207)Pb/(206)Pb for 1) a Pb-mixture representing mine tailings, 2) aerosol Pb-impacted soils within close proximity to the Buick secondary recycling smelter, and 3) an average of soils, rock cores and drill cuttings representing the background conditions. Aqua regia total concentrations and (207)Pb/(206)Pb of mining area dust suggest that 35.4-84.3% of the source Pb in dust is associated with the mine tailings mixture, 9.1-52.7% is associated with the smelter mixture, and 0-21.6% is associated with background materials. Isotope ratios varied minimally within the operational phases of sequential extraction suggesting that mixing of all three Pb mixtures occurs throughout. Labile forms of Pb were attributed to all three end members. The extractable carbonate phase had as much as 96.6% of the total concentration associated with mine tailings, 51.8% associated with smelter deposition, and 34.2% with background. The next most labile geochemical phase (Fe + Mn Oxides) showed similar results with as much as 85.3% associated with mine tailings, 56.8% associated with smelter deposition, and 4.2% associated with the background soil.

  10. Use of Lead Isotopes to Identify Sources of Metal and Metalloid Contaminants in Atmospheric Aerosol from Mining Operations

    Science.gov (United States)

    Félix, Omar I.; Csavina, Janae; Field, Jason; Rine, Kyle P.; Sáez, A. Eduardo; Betterton, Eric A.

    2014-01-01

    Mining operations are a potential source of metal and metalloid contamination by atmospheric particulate generated from smelting activities, as well as from erosion of mine tailings. In this work, we show how lead isotopes can be used for source apportionment of metal and metalloid contaminants from the site of an active copper mine. Analysis of atmospheric aerosol shows two distinct isotopic signatures: one prevalent in fine particles (< 1 μm aerodynamic diameter) while the other corresponds to coarse particles as well as particles in all size ranges from a nearby urban environment. The lead isotopic ratios found in the fine particles are equal to those of the mine that provides the ore to the smelter. Topsoil samples at the mining site show concentrations of Pb and As decreasing with distance from the smelter. Isotopic ratios for the sample closest to the smelter (650 m) and from topsoil at all sample locations, extending to more than 1 km from the smelter, were similar to those found in fine particles in atmospheric dust. The results validate the use of lead isotope signatures for source apportionment of metal and metalloid contaminants transported by atmospheric particulate. PMID:25496740

  11. The lead (Pb) isotope signature, behaviour and fate of traffic-related lead pollution in roadside soils in The Netherlands

    NARCIS (Netherlands)

    Walraven, N.; van Os, B.J.H.; Klaver, G.Th.; Middelburg, J.J.; Davies, G.R.

    2014-01-01

    In this study the origin, behaviour and fate of anthropogenic Pb in sandy roadside soils were assessed by measuring soil characteristics, Pb isotope composition and content. In 1991 and 2003 samples were taken at different depth intervals at approximately 8 and 75 m from two highways in The

  12. Isotopic equilibration between dissolved and suspended particulate lead in the Atlantic Ocean - Evidence from Pb-210 and stable Pb isotopes

    Science.gov (United States)

    Sherrell, Robert M.; Boyle, Edward A.; Hamelin, Bruno

    1992-01-01

    Vertical profiles of, on one hand, the stable Pb isotopic composition, and on the other, the ratio of total Pb to Pb-210 in suspended particles, are noted to closely track contemporaneous depth variations in these ratios for dissolved Pb throughout the upper 2 km of the Sargasso Sea near Bermuda. A simple flux model suggests that the effect of deep ocean scavenging processes on the flux and isotopic composition of Pb sinking on large particles was minor throughout the preanthropogenic, and most of the anthropogenic era: but it has become more important as surface inputs decrease to preleaded gasoline levels, perhaps exceeding the contribution of surface-derived Pb flux in the next decade.

  13. The lead (Pb) isotope signature, behaviour and fate of traffic-related lead pollution in roadside soils in The Netherlands.

    Science.gov (United States)

    Walraven, N; van Os, B J H; Klaver, G Th; Middelburg, J J; Davies, G R

    2014-02-15

    In this study the origin, behaviour and fate of anthropogenic Pb in sandy roadside soils were assessed by measuring soil characteristics, Pb isotope composition and content. In 1991 and 2003 samples were taken at different depth intervals at approximately 8 and 75 m from two highways in The Netherlands. The Pb isotope composition of the litter layer ((206)Pb/(207)Pb=1.12-1.14) differs from the deeper soil samples ((206)Pb/(207)Pb=1.20-1.21). Based on a mixing model it is concluded that the samples contain two Pb sources: natural Pb and anthropogenic Pb, the latter mainly derived from gasoline. (206)Pb/(207)Pb ratios demonstrate that the roadside soils were polluted to a depth of ~15 cm. Within this depth interval, anthropogenic Pb content is associated with organic matter. Although Pb pollution only reached a depth of ~15 cm, this does not mean that the topsoils retain all anthropogenic Pb. Due to the low pH and negligible binding capacity of soils at depths >15 cm, anthropogenic Pb migrated towards groundwater after reaching depths of >15 cm. The Pb isotope composition of the groundwater ((206)Pb/(207)Pb=1.135-1.185) establishes that groundwater is polluted with anthropogenic Pb. The contribution of anthropogenic Pb to the groundwater varies between ~30 and 100%. Based on the difference in soil Pb content and Pb isotope compositions over a period of 12 years, downward Pb migration is calculated to vary from 72 ± 95 to 324 ± 279 mg m(-2)y(-1). Assuming that the downward Pb flux is constant over time, it is calculated that 35-90% of the atmospherically delivered Pb has migrated to the groundwater.

  14. Electron–Rotor Interaction in Organic–Inorganic Lead Iodide Perovskites Discovered by Isotope Effects

    Energy Technology Data Exchange (ETDEWEB)

    Gong, Jue; Yang, Mengjin; Ma, Xiangchao; Schaller, Richard D.; Liu, Gang; Kong, Lingping; Yang, Ye; Beard, Matthew C.; Lesslie, Michael; Dai, Ying; Huang, Baibiao; Zhu, Kai; Xu, Tao

    2016-08-04

    We report on the carrier-rotor coupling effect in perovskite organic-inorganic hybrid lead iodide (CH3NH3PbI3) compounds discovered by isotope effects. Deuterated organic-inorganic perovskite compounds including CH3ND3PbI3, CD3NH3PbI3, and CD3ND3PbI3 were synthesized. Devices made from regular CH3NH3PbI3 and deuterated CH3ND3PbI3 exhibit comparable performance in band gap, current-voltage, carrier mobility, and power conversion efficiency. However, a time-resolved photoluminescence (TRPL) study reveals that CH3NH3PbI3 exhibits notably longer carrier lifetime than that of CH3ND3PbI3, in both thin-film and single-crystal formats. Furthermore, the comparison in carrier lifetime between CD3NH3PbI3 and CH3ND3PbI3 single crystals suggests that vibrational modes in methylammonium (MA+) have little impact on carrier lifetime. In contrast, the fully deuterated compound CD3ND3PbI3 reconfirmed the trend of decreasing carrier lifetime upon the increasing moment of inertia of cationic MA+. Polaron model elucidates the electron-rotor interaction.

  15. Roman road pollution assessed by elemental and lead isotope geochemistry in East Belgium

    Energy Technology Data Exchange (ETDEWEB)

    Renson, Virginie [U.R. Argiles et Paleoclimats, University of Liege, Allee du 6 Aout, B18, Sart Tilman, 4000 Liege (Belgium)], E-mail: vrenson@vub.ac.be; Fagel, Nathalie [U.R. Argiles et Paleoclimats, University of Liege, Allee du 6 Aout, B18, Sart Tilman, 4000 Liege (Belgium); Mattielli, Nadine [Departement des Sciences de la Terre et de l' Environnement, Universite Libre de Bruxelles, CP160/02, Avenue F.D. Roosevelt, 1050 Brussels (Belgium); Nekrassoff, Serge [Station Scientifique des Hautes Fagnes 137, Rue de Botrange, 4950 Robertville (Belgium); Streel, Maurice [U.R.P.P.M., University of Liege, Allee du 6 Aout, B18, Sart Tilman, 4000 Liege (Belgium); De Vleeschouwer, Francois [U.R. Argiles et Paleoclimats, University of Liege, Allee du 6 Aout, B18, Sart Tilman, 4000 Liege (Belgium)

    2008-12-15

    The ability of inorganic geochemistry to record environmental change and especially human impact has been evidenced by several studies across Europe, especially in peat, where it is possible to record the impact of agriculture, mining and other industries. However, despite the numerous investigations on the impact of ancient human activities such as ore mining and smelting, little attention has been paid to geochemistry as a tool to solve problems of palaeopollution in the surroundings of archaeological sites. This paper presents geochemical evidence of the impact of a possible early Roman road built in SE Belgian peatland. Increased Zn and Pb concentrations suggest that Pb-Zn ores were transported on the road. Lead isotope analyses suggest that these ores are locally derived, being compatible with those found in the nearby Pb-Zn ore deposits from East Belgium. Present results provide direct evidence that East Belgian Pb-Zn ores were already being mined during Roman times, i.e. earlier than previously suspected (i.e. 14th century) and that Zn appears to be relatively immobile here. On a broader scale, it also demonstrates that such an early road already had an impact on the environment in terms of metal pollution. This paper enlarges on the range of possibilities offered by geochemistry in the field of geoarchaeology.

  16. Lead isotope ratios in tree bark pockets: An indicator of past air pollution in the Czech Republic

    Energy Technology Data Exchange (ETDEWEB)

    Conkova, M. [Charles University, Faculty of Natural Sciences, Benatska 8, Prague 1 (Czech Republic)], E-mail: conkova@chmi.cz; Kubiznakova, J. [Czech Hydrometeorogical Institute, Na Sabatce 17, Prague 4 (Czech Republic)], E-mail: kubiznakova@chmi.cz

    2008-10-15

    Tree bark pockets were collected at four sites in the Czech Republic with differing levels of lead (Pb) pollution. The samples, spanning 1923-2005, were separated from beech (Fagus sylvatica) and spruce (Picea abies). Elevated Pb content (0.1-42.4 {mu}g g{sup -1}) reflected air pollution in the city of Prague. The lowest Pb content (0.3-2.6 {mu}g g{sup -1}) was found at the Kosetice EMEP 'background pollution' site. Changes in {sup 206}Pb/{sup 207}Pb and {sup 208}Pb/{sup 206}Pb isotope ratios were in agreement with operation times of the Czech main anthropogenic Pb sources. Shortly after the Second World War, the {sup 206}Pb/{sup 207}Pb isotope ratio in bark pockets decreased from 1.17 to 1.14 and the {sup 208}Pb/{sup 206}Pb isotope ratio increased from 2.12 to 2.16. Two dominant emission sources responsible for these changes, lignite and leaded petrol combustion, contributed to the shifts in Pb isotope ratios. Low-radiogenic petrol Pb ({sup 206}Pb/{sup 207}Pb of 1.11) lead to lower {sup 206}Pb/{sup 207}Pb in bark pockets over time. High-radiogenic lignite-derived Pb ({sup 206}Pb/{sup 207}Pb of 1.18 to 1.19) was detected in areas affected by coal combustion rather than by traffic.

  17. Rapid and Highly Sensitive Detection of Lead Ions in Drinking Water Based on a Strip Immunosensor

    Directory of Open Access Journals (Sweden)

    Chuanlai Xu

    2013-03-01

    Full Text Available In this study, we have first developed a rapid and sensitive strip immunosensor based on two heterogeneously-sized gold nanoparticles (Au NPs probes for the detection of trace lead ions in drinking water. The sensitivity was 4-fold higher than that of the conventional LFA under the optimized conditions. The visual limit of detection (LOD of the amplified method for qualitative detection lead ions was 2 ng/mL and the LOD for semi-quantitative detection could go down to 0.19 ng/mL using a scanning reader. The method suffered from no interference from other metal ions and could be used to detect trace lead ions in drinking water without sample enrichment. The recovery of the test samples ranged from 96% to 103%. As the detection method could be accomplished within 15 min, this method could be used as a potential tool for preliminary monitoring of lead contamination in drinking water.

  18. Rapid and highly sensitive detection of lead ions in drinking water based on a strip immunosensor.

    Science.gov (United States)

    Kuang, Hua; Xing, Changrui; Hao, Changlong; Liu, Liqiang; Wang, Libing; Xu, Chuanlai

    2013-03-28

    In this study, we have first developed a rapid and sensitive strip immunosensor based on two heterogeneously-sized gold nanoparticles (Au NPs) probes for the detection of trace lead ions in drinking water. The sensitivity was 4-fold higher than that of the conventional LFA under the optimized conditions. The visual limit of detection (LOD) of the amplified method for qualitative detection lead ions was 2 ng/mL and the LOD for semi-quantitative detection could go down to 0.19 ng/mL using a scanning reader. The method suffered from no interference from other metal ions and could be used to detect trace lead ions in drinking water without sample enrichment. The recovery of the test samples ranged from 96% to 103%. As the detection method could be accomplished within 15 min, this method could be used as a potential tool for preliminary monitoring of lead contamination in drinking water.

  19. Lead isotopes in iron and manganese oxide coatings and their use as an exploration guide for concealed mineralization

    Science.gov (United States)

    Gulson, B.L.; Church, S.E.; Mizon, K.J.; Meier, A.L.

    1992-01-01

    Lead isotopes from Fe and Mn oxides that coat stream pebbles from around the Mount Emmons porphyry molybdenum deposit in Colorado were studied to assess the feasibility of using Pb isotopes to detect concealed mineral deposits. The Fe/Mn oxide coatings were analyzed to determine their elemental concentrations using ICP-AES. The Pb isotope compositions of solutions from a selected suite of samples were measured, using both thermal ionization and ICP mass spectrometry, to compare results determined by the two analytical methods. Heavy mineral concentrates from the same sites were also analyzed to compare the Pb isotope compositions of the Fe/Mn coatings with those found in panned concentrates. The Fe/Mn and 206Pb/204Pb ratios of the oxide coatings are related to the lithology of the host rocks; Fe/Mn oxide coatings on pebbles of black shale have higher Fe/Mn values than do the coatings on either sandstone or igneous rocks. The shale host rocks have a more radiogenic signature (e.g. higher 206Pb/ 204Pb) than the sandstone or igneous host rocks. The Pb isotope data from sandstone and igneous hosts can detect concealed mineralized rock on both a regional and local scale, even though there are contributions from: (1) metals from the main-stage molybdenite ore deposit; (2) metals from the phyllic alteration zone which has a more radiogenic Pb isotope signature reflecting hydrothermal leaching of Pb from the Mancos Shale; (3) Pb-rich base metal veins with a highly variable Pb isotope signature; and (4) sedimentary country rocks which have a more radiogenic Pb isotope signature. An investigation of within-stream variation shows that the Pb isotope signature of the molybdenite ore zone is retained in the Fe/Mn oxide coatings and is not camouflaged by contributions from Pb-rich base-metal veins that crop out upstream. In another traverse, the Pb isotope data from Fe/Mn oxide coatings reflect a complex mixing of Pb from the molybdenite ore zone and its hornfels margin, Pb

  20. A Portable and Power-Free Microfluidic Device for Rapid and Sensitive Lead (Pb2+) Detection

    OpenAIRE

    Lianhui Wang; Shiping Song; Gang Liu; Shijiang He; Chunhui Fan

    2012-01-01

    A portable and power-free microfluidic device was designed for rapid and sensitive detection of lead (Pb2+). 11-mercaptoundecanoic acid (MUA)-functionalized gold nanoparticles (MUA-AuNPs) aggregated in the presence of Pb2+ for the chelation mechanism. When we performed this analysis on a polydimethylsiloxane (PDMS) microfluidic chip, the aggregations deposited onto the surface of chip and formed dark lines along the laminar flows in the zigzag micr...

  1. Rapidity evolution of Wilson lines at the next-to-leading order

    Energy Technology Data Exchange (ETDEWEB)

    Balitsky, Ian [JLAB, Old Dominion U.; Chirilli, Giovanni [LBL

    2013-12-01

    At high energies particles move very fast so the proper degrees of freedom for the fast gluons moving along the straight lines are Wilson-line operators - infinite gauge factors ordered along the line. In the framework of operator expansion in Wilson lines the energy dependence of the amplitudes is determined by the rapidity evolution of Wilson lines. We present the next-to-leading order hierarchy of the evolution equations for Wilson-line operators.

  2. Silica cycling and isotopic composition in northern Marguerite Bay on the rapidly-warming western Antarctic Peninsula

    Science.gov (United States)

    Annett, Amber L.; Henley, Sian F.; Venables, Hugh J.; Meredith, Michael P.; Clarke, Andrew; Ganeshram, Raja S.

    2017-05-01

    The Southern Ocean is a key region for silica (Si) cycling, and the isotopic signatures established here influence the rest of the world's oceans. The climate and ecosystem of the Southern Ocean are changing rapidly, with the potential to impact Si cycling and isotope dynamics. This study examines high-resolution time-series dataset of dissolved Si concentrations and isotopic signatures, particulate Si concentrations and diatom speciation at a coastal site on the western Antarctic Peninsula (WAP), in order to characterise changes in Si cycling with respect to changes occurring in productivity and diatom assemblages. Dissolved and particulate Si phases reflect the dominant control of biological uptake, and combined with isotopic fractionation were consistent with a season of low/intermediate productivity. Biogenic Si is tightly coupled to both chlorophyll and particulate organic carbon at the sampling site, consistent with diatom-dominated phytoplankton assemblages along the WAP. Variability in diatom speciation has a negligible impact on the isotopic signature of dissolved Si in surface waters, although this is unlikely to hold for sediments due to differential dissolution of diatom species. A continued decline in diatom productivity along the WAP would likely result in an increasing unused Si inventory, which can potentially feed back into Si-limited areas, promoting diatom growth and carbon drawdown further afield.

  3. Lead and its isotopes in the sediment of three sites on the Lebanese coast: Identification of contamination sources and mobility

    Energy Technology Data Exchange (ETDEWEB)

    Abi-Ghanem, C., E-mail: carine.a.ghanem@hotmail.fr [Centre National des Sciences Marines, CNRSL, P.O. Box 534, Batroun (Lebanon); Chiffoleau, J.F. [Ifremer, LBCM, Centre de Nantes, BP 21105, F.44311 Nantes cedex 3 (France); Bermond, A. [Agro-ParisTech, 16, rue C. Bernard, F.75231 Paris cedex 5 (France); Nakhle, K.; Khalaf, G. [Centre National des Sciences Marines, CNRSL, P.O. Box 534, Batroun (Lebanon); Borschneck, D. [CEREGE CNRS, Aix-Marseille University, Europole Mediterraneen de l' Arbois, BP 80, 13545 Aix-en-Provence (France); Cossa, D. [Ifremer, LBCM, Centre de Nantes, BP 21105, F.44311 Nantes cedex 3 (France)

    2009-10-15

    Lead concentrations and isotopic composition of sediment samples collected from three sites within the Lebanese coastal zones were measured: at Akkar, Dora and Selaata. Akkar is located far from any direct source of contamination, while Dora and Selaata receive urban and industrial wastes, respectively. Low Pb concentrations (6-16 {mu}g g{sup -1}) were detected in the Akkar sediments, and high concentrations of Pb (70-101 {mu}g g{sup -1}) were detected in the Dora sediments. Measuring stable isotope ratios of Pb makes it possible to identify the principal sources of Pb in the Akkar sediments as Pb emitted from gasoline combustion and Pb originating from natural sources. On the other hand, Pb stable isotopic ratios in Dora sediments indicate that they are more highly influenced by anthropogenic sources. Isotopic Pb ratios in the Selaata deposits, where Pb concentrations range between 5 and 35 {mu}g g{sup -1}, have an exceptional radiogenic signature for marine sediments 1.25 < {sup 206}Pb/{sup 207}Pb < 1.6 and 0.5 < {sup 206}Pb/{sup 208}Pb < 0.67, which shows the impact of the phosphogypsum discharged by Selaata's chemical plant. Isotopic Pb analysis applied to EDTA extracts, to test the mobility of Pb, shows that that this mobility is high (>60%) after 24 h of extraction, and that the extracted Pb is less radiogenic than the residual Pb.

  4. Contrasting origins of the upper mantle revealed by hafnium and lead isotopes from the Southeast Indian Ridge.

    Science.gov (United States)

    Hanan, Barry B; Blichert-Toft, Janne; Pyle, Douglas G; Christie, David M

    2004-11-04

    The origin of the isotopic signature of Indian mid-ocean ridge basalts has remained enigmatic, because the geochemical composition of these basalts is consistent either with pollution from recycled, ancient altered oceanic crust and sediments, or with ancient continental crust or lithosphere. The radiogenic isotopic signature may therefore be the result of contamination of the upper mantle by plumes containing recycled altered ancient oceanic crust and sediments, detachment and dispersal of continental material into the shallow mantle during rifting and breakup of Gondwana, or contamination of the upper mantle by ancient subduction processes. The identification of a process operating on a scale large enough to affect major portions of the Indian mid-ocean ridge basalt source region has been a long-standing problem. Here we present hafnium and lead isotope data from across the Indian-Pacific mantle boundary at the Australian-Antarctic discordance region of the Southeast Indian Ridge, which demonstrate that the Pacific and Indian upper mantle basalt source domains were each affected by different mechanisms. We infer that the Indian upper-mantle isotope signature in this region is affected mainly by lower continental crust entrained during Gondwana rifting, whereas the isotope signature of the Pacific upper mantle is influenced predominantly by ocean floor subduction-related processes.

  5. Carbon isotopes characterize rapid changes in atmospheric carbon dioxide during the last deglaciation

    Science.gov (United States)

    Bauska, Thomas K.; Baggenstos, Daniel; Brook, Edward J.; Mix, Alan C.; Marcott, Shaun A.; Petrenko, Vasilii V.; Schaefer, Hinrich; Lee, James E.

    2016-01-01

    An understanding of the mechanisms that control CO2 change during glacial–interglacial cycles remains elusive. Here we help to constrain changing sources with a high-precision, high-resolution deglacial record of the stable isotopic composition of carbon in CO2 (δ13C-CO2) in air extracted from ice samples from Taylor Glacier, Antarctica. During the initial rise in atmospheric CO2 from 17.6 to 15.5 ka, these data demarcate a decrease in δ13C-CO2, likely due to a weakened oceanic biological pump. From 15.5 to 11.5 ka, the continued atmospheric CO2 rise of 40 ppm is associated with small changes in δ13C-CO2, consistent with a nearly equal contribution from a further weakening of the biological pump and rising ocean temperature. These two trends, related to marine sources, are punctuated at 16.3 and 12.9 ka with abrupt, century-scale perturbations in δ13C-CO2 that suggest rapid oxidation of organic land carbon or enhanced air–sea gas exchange in the Southern Ocean. Additional century-scale increases in atmospheric CO2 coincident with increases in atmospheric CH4 and Northern Hemisphere temperature at the onset of the Bølling (14.6–14.3 ka) and Holocene (11.6–11.4 ka) intervals are associated with small changes in δ13C-CO2, suggesting a combination of sources that included rising surface ocean temperature. PMID:26976561

  6. Unhealthy maternal lifestyle leads to rapid infant weight gain: prevention of future chronic diseases.

    Science.gov (United States)

    Oyama, Mari; Nakamura, Kazutoshi; Tsuchiya, Yasuo; Yamamoto, Masaharu

    2009-01-01

    Infants' rapid (catch-up) weight gain is associated with later obesity and chronic adult diseases. The aim of this study was to determine maternal and environmental factors related to rapid weight gain at one month and 18 months after full-term birth in Japan. Subjects were 1,524 infants and their mothers who visited the 18-month check-up in Niigata City between October 1, 2007 and September 30, 2008. An anonymous questionnaire elicited information on the infant's weight (at birth, 1 month, and 18 months), sex, feeding method, presence of food allergy, gestational age, and caregiver. Mother's information was height, pre-pregnancy weight, pregnancy weight gain, age at delivery, pregnancy toxicosis, number of daily meals during pregnancy, smoking and drinking habits. Some questionnaire items were obtained from a maternal and child health handbook. Independence of predictors for rapid weight gain (vs. slow or average weight gain), i.e. a score gain of 0.67 SD, during the first month and first 18 months was tested by multiple logistic regression analysis. In the first month, having a meal once or twice daily during pregnancy (P = 0.0016) and daily smoking in pre-pregnancy (P = 0.0175) were associated with rapid weight gain. In the first 18 months, use of daycare (P = 0.0083) and daily drinking in pre-pregnancy (P = 0.0130) were associated with rapid weight gain. We conclude that mother's pre-pregnancy smoking and drinking, dieting during pregnancy, and infant daycare attendance lead to rapid infant weight gain. Controlling these factors may prevent future chronic adult lifestyle-related diseases.

  7. The effects of succimer on the absorption of lead in adults determined by using the stable isotope [sup 204]Pb

    Energy Technology Data Exchange (ETDEWEB)

    Smith, D.R. (Univ. of California, San Francisco, CA (United States) Univ. of California, Santa Cruz, CA (United States)); Markowitz, M.E.; Rosen, J.F. (Albert Einstein College of Medicine, Bronx, NY (United States)); Crick, J.; Flegal, A.R. (Univ. of California, Santa Cruz, CA (United States))

    1994-10-01

    The chelating agent succimer (meso-2,3-dimercaptosuccine acid) is orally effective at inducing a urinary lead diuresis and a decrease in blood lead levels in lead poisoned children and adults. However, there are concerns that succimer may increase the absorption of lead from the gastrointestinal (GI) tract during treatment, particularly in cases of continuing lead exposure, which would compromise its effectiveness in reducing whole body lead stores. This preliminary study investigated the effects of succimer on the absorption of lead in adults using a stable lead isotopic tracer ([sup 204]Pb). Twelve male subjects were divided into control (no succimer), 10, and 30 mg succimer/kg body wt treatment groups of 4 individuals each. All subjects ingested a single tracer dose (200 [mu]g) of [sup 204]Pb, followed by a single oral dose of placebo (control) or succimer. Whole blood was collected at intervals of 0, 2, 4, and [approx] 26 hr following ingestion of the [sup 204]Pb tracer, and composite urine and feces samples were collected over the duration of the study ([approx] 26 hr). Mean intestinal excretion of [sup 204]Pb was reduced in the succimer-treated groups compared to the control (placebo), whereas urinary diuresis of [sup 204]Pb was higher in the succimer groups. The amount of lead [sup 204]Pb tracer accounted for at the end of the study was lower in the succimer-treated groups. These results suggest that GI lead absorption was enhanced by succimer and that succimer mediated the redistribution of lead from the circulation to other tissues. However, none of the differences between treatment groups were statistically significant (P < 0.05, t test) because of the relatively large within-group variability. This study demonstrates the utility of microgram doses of a stable lead isotopic tracer to assess the efficacy of clinical chelating agents in humans. 39 refs., 1 fig., 2 tabs.

  8. A "Tail" Of Two Mines: Determining The Sources Of Lead In Mine Waters Using Pb Isotopes

    Science.gov (United States)

    Cousens, B. L.; Allen, D. M.; Lepitre, M. E.; Mortensen, J. K.; Gabites, J. E.; Nugent, M.; Fortin, D.

    2004-12-01

    Acid mine drainage can be a significant environmental problem in regions where mine tailings are exposed to surface water and shallow groundwater flow. Whereas high metal concentrations in surface waters and groundwaters indicate that metals are being mobilized, these data do not uniquely identify the source of the contamination. The isotopic composition of Pb in mine waters is a superb tracer of Pb sources, because the isotopic composition of ore Pb is usually significantly different from that of host rocks, other surficial deposits, and aerosols. We have investigated metal mobility at two abandoned Pb-Zn mines in different geological settings: the sediment-hosted Sullivan Mine in southeastern British Columbia, and the New Calumet Mine of western Quebec that is hosted in metamorphic rocks of the Grenville Province. Ores from both mines have homogeneous Pb isotopic compositions that are much less radiogenic than surrounding host rocks. At Sullivan, the Pb isotopic compositions of water samples define a mixing line between Sullivan ore and at least one other more radiogenic end-member. Water samples with high Pb concentrations (0.002 to 0.3 mg/L) generally are acidic and have Pb isotope ratios equal to Sullivan ore, whereas waters with low Pb contents have near-neutral pH and have variably more radiogenic Pb isotope ratios. Thus not all the waters collected in the study area originate from Sullivan ore or mining operations, as previously thought. The dominant source of ore Pb in mine waters are the waste rock dumps. Based on their isotopic compositions, host shales or aerosols from the local Pb smelter are potential sources of non-Sullivan ore Pb; local glacial tills are an unlikely source due to their heterogeneous Pb isotopic composition. Similarly, at the New Calumet mine, water samples collected in direct contact with either ore at the surface or tailings have high Pb concentrations (up to 0.02 mg/L) and Pb isotope ratios equal to New Calumet Pb-Zn ore. However

  9. Lead isotopes tracing the life cycle of a catchment: From source rock via weathering to human impact

    Science.gov (United States)

    Negrel, P. J.; Petelet-Giraud, E.; Guerrot, C.; Millot, R.

    2015-12-01

    Chemical weathering of rocks involves consumption of CO2, a greenhouse gas with a strong influence on climate. Among rocks exposed to weathering, basalt plays a major role in the carbon cycle as it is more easily weathered than other crystalline silicate rocks. This means that basalt weathering acts as a major atmospheric CO2 sink. The present study investigated the lead isotopes in rock, soil and sediment for constraining the life cycle of a catchment, covering source rocks, erosion processes and products, and anthropogenic activities. For this, we investigated the Allanche river drainage basin in the Massif Central, the largest volcanic areas in France, that offers opportunities for selected geochemical studies since it drains a single type of virtually unpolluted volcanic rock, with agricultural activity increasing downstream. Soil and sediment are derived exclusively from basalt weathering, and their chemistry, coupled to isotope tracing, should shed light on the behavior of chemical species during weathering from parental bedrock. Bedrock samples of the basin, compared to regional bedrock of the volcanic province, resulted from a complex history and multiple mantle reservoir sources and mixing. Regarding soils and sediments, comparison of Pb and Zr normalized to mobile K shows a linear evolution of weathering processes, whereby lead enrichment from atmospheric deposition is the other major contributor. Lead-isotope ratios showed that most of the lead budget in sediment and soil results from bedrock weathering with an influence of past mining and mineral processing of ores in the Massif Central, and deposition of lead-rich particles from gasoline combustion, but no lead input from agricultural activity. A classic box model was used to investigate the dynamics of sediment transfer at the catchment scale, the lead behavior in the continuum bedrock-soil-sediment and the historical evolution of anthropogenic aerosol emissions.

  10. A stable lead isotopic investigation of the use of sycamore tree rings as a historical biomonitor of environmental lead contamination.

    Science.gov (United States)

    Patrick, Gavin J; Farmer, John G

    2006-06-01

    The validity of the use of sycamore (Acer pseudoplatanus) tree-rings for the reconstruction of atmospheric lead pollution histories was investigated. Tree cores spanning 1892-2003 were collected from several sycamores from the eastern shore of Loch Lomond, Scotland, an area with no local point sources of lead emission. The lead concentration and 206Pb/207Pb profiles of the Loch Lomond region cores were compared with corresponding data for the 210Pb-dated loch sediment, and also with data for moss of known age from a Scottish herbarium collection. Two of the seven sycamore cores showed the same lead concentration trend as the lead flux to the loch, the rest having no similarity to either each other or the loch sediment record. Two further sycamore cores showed some similarity in their temporal 206Pb/207Pb trends to those seen in the sediment and moss records, but only in part of their profiles, whilst the 206Pb/207Pb ratios of the other sycamore cores remained relatively unchanged for the majority of the time covered, or exhibited an opposite trend. The 206Pb/207Pb ratios of the tree cores were also mostly higher than those of the previously established records for any given time period. Tree cores covering 1878-2002 were also collected along transects from Wanlockhead and Tyndrum, two areas of former lead mining and smelting associated with distinct 206Pb/207Pb ratios of 1.170 and 1.144, respectively. The Wanlockhead tree cores exhibited a generally decreasing trend in lead concentration with both time and distance from the lead mine. The characteristic 206Pb/207Pb ratio of 1.170 was observed in samples close to the mine but a decrease in the influence of the mine-derived lead was observed in more distant samples. The tree sampled at Tyndrum showed elevated lead concentrations, which decreased with time, and a fairly constant 206Pb/207Pb ratio of 1.15 reflecting input from the mine, features not observed in any other trees along the transect. Overall the data

  11. Helium and lead isotopes reveal the geochemical geometry of the Samoan plume.

    Science.gov (United States)

    Jackson, M G; Hart, S R; Konter, J G; Kurz, M D; Blusztajn, J; Farley, K A

    2014-10-16

    Hotspot lavas erupted at ocean islands exhibit tremendous isotopic variability, indicating that there are numerous mantle components hosted in upwelling mantle plumes that generate volcanism at hotspots like Hawaii and Samoa. However, it is not known how the surface expression of the various geochemical components observed in hotspot volcanoes relates to their spatial distribution within the plume. Here we present a relationship between He and Pb isotopes in Samoan lavas that places severe constraints on the distribution of geochemical species within the plume. The Pb-isotopic compositions of the Samoan lavas reveal several distinct geochemical groups, each corresponding to a different geographic lineament of volcanoes. Each group has a signature associated with one of four mantle endmembers with low (3)He/(4)He: EMII (enriched mantle 2), EMI (enriched mantle 1), HIMU (high µ = (238)U/(204)Pb) and DM (depleted mantle). Critically, these four geochemical groups trend towards a common region of Pb-isotopic space with high (3)He/(4)He. This observation is consistent with several low-(3)He/(4)He components in the plume mixing with a common high-(3)He/(4)He component, but not mixing much with each other. The mixing relationships inferred from the new He and Pb isotopic data provide the clearest picture yet of the geochemical geometry of a mantle plume, and are best explained by a high-(3)He/(4)He plume matrix that hosts, and mixes with, several distinct low-(3)He/(4)He components.

  12. Geogenic lead isotope signatures from meat products in Great Britain: Potential for use in food authentication and supply chain traceability

    Energy Technology Data Exchange (ETDEWEB)

    Evans, Jane A.; Pashley, Vanessa [NIGL, BGS, Keyworth, NG12 5GG (United Kingdom); Richards, Gemma J. [School of Veterinary Science, University of Bristol, Bristol BS40 5DU (United Kingdom); Brereton, Nicola [The Food and Environment Research Agency, Sand Hutton, York YO41 1LZ (United Kingdom); Knowles, Toby G. [School of Veterinary Science, University of Bristol, Bristol BS40 5DU (United Kingdom)

    2015-12-15

    This paper presents lead (Pb) isotope data from samples of farm livestock raised in three areas of Britain that have elevated natural Pb levels: Central Wales, the Mendips and the Derbyshire Peak District. This study highlights three important observations; that the Pb found in modern British meat from these three areas is geogenic and shows no clear evidence of modern tetraethyl anthropogenic Pb contribution; that the generally excellent match between the biological samples and the ore field data, particularly for the Mendip and Welsh data, suggests that this technique might be used to provenance biological products to specific ore sites, under favourable conditions; and that modern systems reflect the same process of biosphere averaging that is analogous to cultural focusing in human archaeological studies that is the process of biological averaging leading to an homogenised isotope signature with increasing Pb concentration. - Highlights: • Lead (Pb) isotopes measured in modern British meat were geogenic in origin. • The match indicates that this technique may be used to provenance biological products. • There was no evidence for a contribution from modern anthropogenic Pb sources.

  13. A portable and power-free microfluidic device for rapid and sensitive lead (Pb2+) detection.

    Science.gov (United States)

    Fan, Chunhui; He, Shijiang; Liu, Gang; Wang, Lianhui; Song, Shiping

    2012-01-01

    A portable and power-free microfluidic device was designed for rapid and sensitive detection of lead (Pb(2+)). 11-mercaptoundecanoic acid (MUA)-functionalized gold nanoparticles (MUA-AuNPs) aggregated in the presence of Pb(2+) for the chelation mechanism. When we performed this analysis on a polydimethylsiloxane (PDMS) microfluidic chip, the aggregations deposited onto the surface of chip and formed dark lines along the laminar flows in the zigzag microchannels. This visual result can be observed by the naked eye through a microscope or just a drop of water as a magnifier. Ten μM Pb(2+) was successfully detected.

  14. Re-estimation of argon isotope ratios leading to a revised estimate of the Boltzmann constant

    Science.gov (United States)

    de Podesta, Michael; Mark, Darren F.; Dymock, Ross C.; Underwood, Robin; Bacquart, Thomas; Sutton, Gavin; Davidson, Stuart; Machin, Graham

    2017-10-01

    In 2013, NPL, SUERC and Cranfield University published an estimate for the Boltzmann constant (de Podesta et al 2013 Metrologia 50 354-76) based on a measurement of the limiting low-pressure speed of sound in argon gas. Subsequently, an extensive investigation by Yang et al (2015 Metrologia 52 S394-409) revealed that there was likely to have been an error in the estimate of the molar mass of the argon used in the experiment. Responding to Yang et al (2015 Metrologia 52 S394-409), de Podesta et al revised their estimate of the molar mass (de Podesta et al 2015 Metrologia 52 S353-63). The shift in the estimated molar mass, and of the estimate of k B, was large:  -2.7 parts in 106, nearly four times the original uncertainty estimate. The work described here was undertaken to understand the cause of this shift and our conclusion is that the original samples were probably contaminated with argon from atmospheric air. In this work we have repeated the measurement reported in de Podesta et al (2013 Metrologia 50 354-76) on the same gas sample that was examined in Yang et al (2015 Metrologia 52 S394-409) and de Podesta et al (2015 Metrologia 52 S353-63). However in this work we have used a different technique for sampling the gas that has allowed us to eliminate the possibility of contamination of the argon samples. We have repeated the sampling procedure three times, and examined samples on two mass spectrometers. This procedure confirms the isotopic ratio estimates of Yang et al (2015 Metrologia 52 S394-409) but with lower uncertainty, particularly in the relative abundance ratio R 38:36. Our new estimate of the molar mass of the argon used in Isotherm 5 in de Podesta et al (2013 Metrologia 50 354-76) is 39.947 727(15) g mol-1 which differs by  +0.50 parts in 106 from the estimate 39.947 707(28) g mol-1 made in de Podesta et al (2015 Metrologia 52 S353-63). This new estimate of the molar mass leads to a revised estimate of the Boltzmann constant of k B

  15. Lead and neodymium isotopic results from metabasalts of the Haveri Formation, southern Finland: evidence for Palaeoproterozoic enriched mantle

    Directory of Open Access Journals (Sweden)

    Vaasjoki, M.

    1999-06-01

    Full Text Available Tholeiitic metabasalts and coexisting sulphides have been analysed for their Pb and Nd isotopic compositions from the Proterozoic Haveri Formation, which forms the basal unit of the Tampere Schist Belt in southern Finland. Ten whole rock samples analysed for Pb isotopes form a sublinear array which yields rather uncertain age estimates in the 1900-2000 Ma range and lies on the 207Pb/204Pb vs. 206Pb/204Pb diagram well below the average global lead evolution curve. The initial lead isotopic composition inferred from the whole rock data and measured on chalcopyrite is the least radiogenic obtained from the Svecofennian domain, and precludes involvement of old upper crustal material in basalt genesis. This together with the geochemical composition and initial eNd (1900 of +0.5±0.6 suggest that the Haveri mafic metavolcanic rocks were not derived from convective MORB-type mantle. The source was rather a mantle, which had been enriched in LREE for a considerable time period. Some chalcopyrite trace leads plot close to the whole rock array while others lie above it. This is interpreted as indicating two distinct mineralisation processes. The primary and major process involved lead which was cogenetic with the basalts, while the second mineralising fluid introduced radiogenic (high 207Pb upper crustal lead scavenged from the adjacent sedimentary rocks. The least radiogenic leads at Haveri and in the Outokumpu ophiolite complex some 300 km NE are similar and the two occurrences can be coeval. The preservation of original mantle material at Haveri may be interpreted as suggesting that continental crust had formed in the Tampere area 1900-2000 Ma ago.

  16. Lead and stable lead isotope ratios in soil, earthworms, and bones of American woodcock (Scolopax minor) from eastern Canada.

    Science.gov (United States)

    Scheuhammer, Anton M; Bond, Della E; Burgess, Neil M; Rodrigue, Jean

    2003-11-01

    A study to discriminate among different possible sources of elevated Pb exposure for American woodcock (Scolopax minor) in eastern Canada is described. Undamaged wing bones excised from young-of-the-year woodcock collected from several locations in southern Ontario, southern Quebec, New Brunswick, and Nova Scotia, Canada, along with soil and earthworm (Aporrectodea tuberculata and Lumbricus rubellus) samples from the same sites, were analyzed for total Pb, and stable Pb isotopes. Ignoring six soil samples with high (> 60 microg/g) Pb concentration from the vicinity of Montreal (QC, Canada), the mean soil-Pb concentration for all sites combined was 19 microg/g (dry wt; n = 64), with a mean 206Pb:207Pb ratio of 1.19, values typical for uncontaminated rural soils in eastern North America. In earthworms, Pb concentrations ranged from 2.4 to 865 (microg/g [dry wt], mean = 24 microg/g). Concentrations of Pb in worms and soils were positively correlated (r = 0.71; p 20 microg/g) had 206Pb:207Pb ratios substantially different from worms and soils sampled from the same areas, even though woodcock feed extensively on soil invertebrates, especially earthworms. The range of 206Pb:207Pb ratios in wing bones of woodcock with elevated Pb exposure was not consistent with exposure to environmental Pb from past gasoline combustion nor Precambrian mining wastes but was consistent with ingestion of spent Pb shotgun pellets.

  17. Sulfate-water isotope geothermometry and lead isotope data for the regional geothermal system in the Twin Falls area, south-central Idaho

    Science.gov (United States)

    Mariner, R.H.; Young, H.W.; Bullen, T.D.; Janik, C.J.; ,

    1997-01-01

    Sulfate-water isotope geothermometry for the geothermal system at Twin Falls, Idaho indicates aquifer-temperatures of 90?? to 106 ??C; most sites are between 90?? and 93 ??C. 206Pb/204pb and 280Pb/204Pb of individual thermal waters are principally a function of how much lead has been dissolved from the carbonate and silicate fractions of the Paleozoic limestone collected west of Grand View Peak. Although most thermal waters are recovered from Tertiary rhyolite, very little of the dissolved lead is from the rhyolite. Recharge to this system occurs in northern Nevada and the fluid moves northward in the Paleozoic limestones. The occurrence of thermal fluid in the Idavada Volcanics near and south of Twin Falls, Idaho is the result of upward movement of this fluid from the Paleozoic limestone.

  18. Isotopic characterisation of lead in contaminated soils from the vicinity of a non-ferrous metal smelter near Plovdiv, Bulgaria

    Energy Technology Data Exchange (ETDEWEB)

    Bacon, Jeffrey R. [Macaulay Institute, Craigiebuckler, Aberdeen AB15 8QH (United Kingdom)]. E-mail: j.bacon@macaulay.ac.uk; Dinev, Nikolai S. [N Poushkarov Institute of Soil Science and Agroecology, Sofia (Bulgaria)

    2005-03-01

    Soil samples from the vicinity of a non-ferrous metal smelter near Plovdiv, Bulgaria contained very high concentrations of cadmium, lead and zinc (up to 140, 4900 and 5900 mg kg{sup -1}, respectively). A roadside soil in a relatively uncontaminated area also contained high concentrations of the same metals (24, 1550 and 1870 mg kg{sup -1}, respectively) indicating that the transport of ores could be a source of contamination. Even though the lead isotope ratios in all the samples fell within a very narrow range (for example, 1.186-1.195 for {sup 206}Pb/{sup 207}Pb), the samples could be differentiated into three distinct groups: ores ({sup 206}Pb/{sup 207}Pb and {sup 208}Pb/{sup 207}Pb ratios of 1.1874-1.1884 and 2.4755-2.4807, respectively), current deposition (1.1864 and 2.4704-2.4711, respectively) and local background (1.1927-1.1951 and 2.4772-2.4809, respectively). Although most of the current deposition has its origin in the ores used at the smelter, up to 12% could be from other sources such as petrol lead. - Although soils in the vicinity of a non-ferrous metal smelter near Plovdiv, Bulgaria, have become highly contaminated with the ores used, lead isotope analysis has revealed that up to 12% of current deposition could be from other sources such as petrol lead.

  19. Lead isotope evidence for a young formation age of the Earth-Moon system

    Science.gov (United States)

    Connelly, J. N.; Bizzarro, M.

    2016-10-01

    A model of a giant impact between two planetary bodies is widely accepted to account for the Earth-Moon system. Despite the importance of this event for understanding early Earth evolution and the inventory of Earth's volatiles critical to life, the timing of the impact is poorly constrained. We explore a data-based, two-stage Pb isotope evolution model in which the timing of the loss of volatile Pb relative to refractory U in the aftermath of the giant impact is faithfully recorded in the Pb isotopes of bulk silicate Earth. Constraining the first stage Pb isotopic evolution permits calculating an age range of 4.426-4.417 Ga for the inflection in the U/Pb ratio related to the giant impact. This model is supported by Pb isotope data for angrite meteorites that we use to demonstrate volatility-driven, planetary-scale Pb loss was an efficient process during the early Solar System. The revised age is ∼100 Myr younger than most current estimates for the age of the Moon but fully consistent with recent ages for lunar ferroan anorthosite and the timing of Earth's first crust inferred from the terrestrial zircon record. The estimated loss of ∼98% of terrestrial Pb relative to the Solar System bulk composition by the end of the Moon-forming process implies that the current inventory of Earth's most volatile elements, including water, arrived during post-impact veneering by volatile-rich bodies.

  20. Coupled study of radionuclides and stable lead isotopes in Western Mediterranean; Etude couplee des radionucleides et des isotopes stables du plomb en Mediterranee occidentale

    Energy Technology Data Exchange (ETDEWEB)

    Miralles, J

    2004-05-15

    The aim of this work is to identified an environmental deposit able to have stored the atmospheric signal over large time-scale leaning our investigations on lead stable isotopes ({sup 206}Pb, {sup 207}Pb, {sup 208}Pb) and radionuclide ({sup 210}Pb, {sup 137}Cs, {sup 239}Pu, {sup 240}Pu) analysis. Owing to prior studies on anthropogenic lead sources, emission intensity and sedimentary accumulation, we choose to investigate the marine sediments of the Western Mediterranean. In the Gulf of Lions, the sedimentary accumulation is 110 {+-} 7 {mu}g.cm{sup -2} high in good agreement with the atmospheric inventory estimate we made from salt marshes of Camargue (99 {mu}g.cm{sup -2}). The reconstructed lead accumulation through a modelling step coupling {sup 210}Pb and stable isotopes corroborates the regional anthropogenic emissions (Ferrand, 1996). Briefly, in this context of the marine sediments are a relevant proxy to study past lead atmospheric concentration over the last hundred years. In the Alboran Sea, the study area is less constrained and more complex in terms of climatic, meteorological and hydrological conditions. The sedimentary inventory is of 153 {+-} 47 {mu}g.cm{sup -2}, 1,5 higher than in the margin sediments of the Gulf of Lions. The analysis of aerosols, sediments and settling particles evidences a continuity between the atmospheric signal and the sedimentary record. In spite of this encouraging results, the knowledge of the Alboran system is still too restricted in order to unambiguously conclude on accuracy of deep marine sediments of this area to study past atmospheric fallouts. (author)

  1. Lead isotope evidence for recent uranium mobility in geological formations of Brazil: implications for radioactive waste disposal

    Energy Technology Data Exchange (ETDEWEB)

    Iyer, S.S. [Department of Physics and Astronomy, University of Calgary, Calgary (Canada); Babinski, M. [Instituto de Geociencias, Universidade de Sao Paulo, Sao Paulo (Brazil); Marinho, M.M. [Companhia Baiana de Pesquisa Mineral (CBPM), Salvador (Brazil); Barbosa, J.S.F. [Instituto de Geociencias, Universidade Federal da Bahia, Salvador (Brazil); Sato, I.M.; Salvador, V.L. [Instituto de Pesquisas Energeticas e Nucleares (CNEN/SP), Sao Paulo (Brazil)

    1999-03-01

    Lead-lead isotope data from whole rock samples are used to investigate the recent (last few million years) mobility of U and Th. The method is based on the comparison of the calculated present day U and Th concentrations required to yield the Pb isotope composition in the samples with the actual present day concentrations of U and Th obtained by direct measurement. The geological formations studied include the Neoproterozoic carbonate sediments of the Bambui Group, Archean/Paleoproterozoic granite-greenstone terrain of the Contendas-Mirante Complex and a Proterozoic ortho-gneisses hosting U deposit in Lagoa Real. All these formations are in the Sao Francisco Craton, Brazil. The data show high U mobility in the carbonate sediments and in the deformed ortho-gneisses set in a ductile shear zone. Infiltration of groundwater through fault zones seems to have facilitated the U mobility. The Pb isotope approach is a useful technique complementing U-series disequilibrium studies and may be included for site characterization studies for radioactive waste disposal. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

  2. Carbon and Nitrogen Isotopes from Top Predator Amino Acids Reveal Rapidly Shifting Ocean Biochemistry in the Outer California Current

    Science.gov (United States)

    Ruiz-Cooley, Rocio I.; Koch, Paul L.; Fiedler, Paul C.; McCarthy, Matthew D.

    2014-01-01

    Climatic variation alters biochemical and ecological processes, but it is difficult both to quantify the magnitude of such changes, and to differentiate long-term shifts from inter-annual variability. Here, we simultaneously quantify decade-scale isotopic variability at the lowest and highest trophic positions in the offshore California Current System (CCS) by measuring δ15N and δ13C values of amino acids in a top predator, the sperm whale (Physeter macrocephalus). Using a time series of skin tissue samples as a biological archive, isotopic records from individual amino acids (AAs) can reveal the proximate factors driving a temporal decline we observed in bulk isotope values (a decline of ≥1 ‰) by decoupling changes in primary producer isotope values from those linked to the trophic position of this toothed whale. A continuous decline in baseline (i.e., primary producer) δ15N and δ13C values was observed from 1993 to 2005 (a decrease of ∼4‰ for δ15N source-AAs and 3‰ for δ13C essential-AAs), while the trophic position of whales was variable over time and it did not exhibit directional trends. The baseline δ15N and δ13C shifts suggest rapid ongoing changes in the carbon and nitrogen biogeochemical cycling in the offshore CCS, potentially occurring at faster rates than long-term shifts observed elsewhere in the Pacific. While the mechanisms forcing these biogeochemical shifts remain to be determined, our data suggest possible links to natural climate variability, and also corresponding shifts in surface nutrient availability. Our study demonstrates that isotopic analysis of individual amino acids from a top marine mammal predator can be a powerful new approach to reconstructing temporal variation in both biochemical cycling and trophic structure. PMID:25329915

  3. Predicting 13C-18O clumped isotope fractionation in dissolved inorganic carbon and rapidly precipitated carbonate minerals

    Science.gov (United States)

    Hill, P. S.; Tripati, A. K.; Schauble, E. A.

    2012-12-01

    The occurrence of multiply substituted isotopologues in carbonates forms the basis for clumped isotope thermometry. It is important to understand how clumping may be affected by environmental factors under both equilibrium and disequilbrium conditions. "Clumping" of heavy isotopes into bonds with each other in dissolved inorganic carbon (DIC) species is of particular interest because natural carbonates that precipitate too rapidly to reach internal isotopic exchange equilibrium may instead inherit the clumping signature of DIC in the parent solution. DIC speciation is dependent on pH, suggesting that clumping signatures inherited by rapidly precipitated carbonate minerals could also be affected by pH. To better understand these disequilibrium clumped isotope signatures (and their effects on inferred temperatures of formation), we have developed theoretical models of the individual DIC species, composite DIC solutions, and bulk carbonate minerals. We used 4 different techniques for modelling the hydration of DIC: gas phase, implicit solvation, explicit solvation (ion with 3 water molecules) and supermolecular clusters (ion plus 21 to 32 water molecules with geometries generated by molecular dynamics). For each solvation technique, we performed sensitivity testing by combining different levels of theory (7 ab initio/hybrid methods, each with 5 different sizes of basis sets) to understand the limits of each technique. We looked at the degree of convergence with the most complex (and accurate) models in order to select the most reliable and efficient modelling methods. Overall, our models predict a difference between Δ47 ( HCO3-) and Δ47 (CO32-) > .025‰, enough to potentially perturb inferred formation temperatures by ≥ 5°C. This difference is fairly consistent at most levels of theory we tested. The models also predict that a carbonate mineral precipitating very rapidly (i.e., forming under isotopic disequilibrium conditions) in a DIC solution of low to

  4. Deep inelastic scattering with leading protons or large rapidity gaps at HERA

    Energy Technology Data Exchange (ETDEWEB)

    Chekanov, S.; Derrick, M.; Magill, S. [Argonne National Lab., Argonne, IL (US)] (and others)

    2008-12-15

    The dissociation of virtual photons, {gamma}{sup *}p{yields} Xp, in events with a large rapidity gap between X and the outgoing proton, as well as in events in which the leading proton was directly measured, has been studied with the ZEUS detector at HERA. The data cover photon virtualities Q{sup 2}> 2 GeV{sup 2} and {gamma}{sup *}p centre-of-mass energies 40 2 GeV, where M{sub X} is the mass of the hadronic final state, X. Leading protons were detected in the ZEUS leading proton spectrometer. The cross section is presented as a function of t, the squared four-momentum transfer at the proton vertex and {phi}, the azimuthal angle between the positron scattering plane and the proton scattering plane. It is also shown as a function of Q{sup 2} and x{sub P}, the fraction of the proton's momentum carried by the diffractive exchange, as well as {beta}, the Bjorken variable defined with respect to the diffractive exchange. (orig.)

  5. Pyrite multiple-sulfur isotope evidence for rapid expansion and contraction of the early Paleoproterozoic seawater sulfate reservoir

    Science.gov (United States)

    Scott, Clint; Wing, Boswell A.; Bekker, Andrey; Planavsky, Noah J.; Medvedev, Pavel; Bates, Steven M.; Yun, Misuk; Lyons, Timothy W.

    2014-03-01

    Earth's oxygenation is often described in terms of two unidirectional steps at the beginning and end of the Proterozoic Eon, separated by a long-lived intermediate redox state. Recent work defines a more complicated path to oxygenation, exemplified by an apparent drop in oxidation state following the early Paleoproterozoic Lomagundi carbon isotope excursion. The timing of this proposed drop in oxidation state is not well constrained, and it is not clear how it relates to redox conditions during the remainder of the Proterozoic. Here we present a study of pyrite multiple-sulfur isotopes, supported by Fe speciation and organic carbon isotopes, from early Paleoproterozoic black shales. We find evidence for the rapid expansion of the seawater sulfate reservoir during the Great Oxidation Event at ca. 2.3 Ga followed by a subsequent contraction in the size of the seawater sulfate reservoir at ca. 2.05 Ga. This scenario is consistent with the emerging view of a rise and fall in surface oxidation state during the early Paleoproterozoic. Comparison of our new data to other records of the seawater sulfate reservoir suggests that the elevated sulfate concentrations that characterize the early Paleoproterozoic did not return until the late Neoproterozoic.

  6. The persistence of lead from past gasoline emissions and mining drainage in a large riparian system: Evidence from lead isotopes in the Sacramento River, California

    Science.gov (United States)

    Dunlap, C.E.; Alpers, C.N.; Bouse, R.; Taylor, H.E.; Unruh, D.M.; Flegal, A.R.

    2008-01-01

    Lead concentrations and isotope ratios measured in river water colloids and streambed sediment samples along 426 km of the Sacramento River, California reveal that the influence of lead from the historical mining of massive sulfide deposits in the West Shasta Cu-mining district (at the headwaters of the Sacramento River) is confined to a 60 km stretch of river immediately downstream of that mining region, whereas inputs from past leaded gasoline emissions and historical hydraulic Au-mining in the Sierra Nevadan foothills are the dominant lead sources in the remaining 370 km of the river. Binary mixing calculations suggest that more than 50% of the lead in the Sacramento River outside of the region of influence of the West Shasta Cu-mining district is derived from past depositions of leaded gasoline emissions. This predominance is the first direct documentation of the geographic extent of gasoline lead persistence throughout a large riparian system (>160,000 km2) and corroborates previous observations based on samples taken at the mouth of the Sacramento River. In addition, new analyses of sediment samples from the hydraulic gold mines of the Sierra Nevada foothills confirm the present-day fluxes into the Sacramento River of contaminant metals derived from historical hydraulic Au-mining that occurred during the latter half of the 19th and early part of the 20th centuries. These fluxes occur predominantly during periods of elevated river discharge associated with heavy winter precipitation in northern California. In the broadest context, the study demonstrates the potential for altered precipitation patterns resulting from climate change to affect the mobility and transport of soil-bound contaminants in the surface environment. ?? 2008 Elsevier Ltd.

  7. Historical lead isotope record of a sediment core from the Derwent River (Tasmania, Australia): a multiple source environment.

    Science.gov (United States)

    Townsend, Ashley T; Seen, Andrew J

    2012-05-01

    A 105 cm sediment core from the Derwent River (Tasmania, Australia) was collected in 2004 and was characterised considering both physical (loss on ignition at 550 °C and grain size) and chemical (Fe, Cu, Zn, Cd and Pb concentrations, Pb isotope ratios and (210)Pb dating) properties. The core was analysed to (i) investigate the historical profiles of some important elements associated with the Risdon zinc refinery adjacent to the Derwent River, (ii) determine Pb isotopic signatures of sediment samples, and (iii) assess the veracity of Pb isotope ratios as indicators of contaminant Pb input. Extractable metal concentrations were (all values as mgkg(-1), non-normalised for grain size) Fe: 20,000-35,000, Zn: 42-4500, Pb: 5-1090, Cu: 13-141, and Cd: 1-31; with a close correlation between Cu, Zn, Cd and Pb. Metal enrichment factors (normalised to Al) were Pb: 0.9-144, Zn: 0.8-93, Cd: 0.8-30, Cu: 0.8-8.9 and Fe: 0.9-1.3, confirming anthropogenic contributions of Cu, Zn, Pb and Cd to the sediments. The onset of metal contamination above background levels occurred at a depth between 43 and 49 cm, with maximum concentrations noted near 20 cm for Cu, Zn, Cd and Pb. Lead isotope ratios were determined in sediments using sector field ICP-MS, and were found to be 36.5-38.8, 16.5-18.7 and 1.07-1.20 for (208)Pb/(204)Pb, (206)Pb/(204)Pb and (206)Pb/(207)Pb ratios, respectively. Major Australian ores processed at the refinery over the previous ~90 years include those from Broken Hill, Rosebery, Mt Isa, Elura, Hellyer and Century deposits. Anthropogenic impact by Pb with Broken Hill type isotopic ratio was initially evident in the core at 43-49 cm. The introduction of Rosebery and Elura ores to the refinery was also clearly noted. Pb isotope ratios further highlight that the Derwent River has been exposed to a greater impact by anthropogenic Pb in comparison to other major Tasmanian rivers, namely the Huon and Tamar.

  8. Spatial Distribution of Lead Isotope Ratios and Inorganic Element Concentrations in Epiphytic Lichens from the Athabasca Oil Sands Region

    Science.gov (United States)

    Graney, J. R.; Landis, M. S.; Puckett, K.; Edgerton, E.; Krupa, S.; Percy, K.

    2013-12-01

    Coupled studies of inorganic element concentrations and lead (Pb) isotope ratios have been conducted on Hypogymnia physodes samples collected in the Athabasca Oil Sands Region (AOSR) in Alberta, Canada in 2002, 2008, and 2011. To investigate the spatial extent of air emissions, the lichens were collected from sites as far as 160 km from the mining and processing operations. 30 milligram sub-samples of the lichens were microwave digested, and the extracts were analyzed using DRC-ICPMS to determine elemental concentrations, and sector field ICPMS to measure Pb isotope ratios. Concentrations of elements in the lichens were found to reflect proximity to mining and oil processing sites as well as topography, ecosystem differences, and the metabolic biogeochemistry of the lichens. An exponential decrease in concentration of metals associated with fugitive dust (aluminum and others) versus distance from the mining sites, suggests elevated coarse particle emissions associated with mining operations. Near source concentrations of metals with an oil signature (vanadium and others) are less enhanced and more homogeneous than the metals in the fugitive dust, reflecting emission and deposition of smaller diameter particles at greater distances from oil processing sources. The mining and oil processing signatures are superimposed over elemental concentrations that reflect the nutrient needs of the lichens. These findings are being confirmed through ongoing studies using dichot samplers to collect coarse and fine particulate aerosol samples. The lichen samples collected beyond 50 km from the mining and processing sites cluster into a Pb isotope grouping with a 207Pb / 206Pb ratio of 0.8650 and a 208Pb / 206Pb ratio near 2.095. This grouping likely reflects the regional background Pb isotope ratio signature. 207Pb / 206Pb and 208Pb / 206Pb ratios decrease as one nears the mining and processing operations. This indicates that other Pb source(s), (e.g. Pb in the bitumen from the oil

  9. Isotopic identification of natural vs. anthropogenic lead sources in marine sediments from the inner Ria de Vigo (NW Spain)

    Energy Technology Data Exchange (ETDEWEB)

    Alvarez-Iglesias, P., E-mail: palvarez@uvigo.es [Department of Marine Geosciences and Land Use Management, Faculty of Marine Sciences, University of Vigo (Spain); Laboratorio de Analisis Quimico Instrumental, C.A.C.T.I., Universidad de Vigo (Spain); Rubio, B., E-mail: brubio@uvigo.es [Department of Marine Geosciences and Land Use Management, Faculty of Marine Sciences, University of Vigo (Spain); Millos, J., E-mail: jmillos@uvigo.es [Laboratorio de Analisis Quimico Instrumental, C.A.C.T.I., Universidad de Vigo (Spain)

    2012-10-15

    San Simon Bay, the inner part of the Ria de Vigo (NW Spain), an area previously identified as highly polluted by Pb, was selected for the application of Pb stable isotope ratios as a fingerprinting tool in subtidal and intertidal sediment cores. Lead isotopic ratios were determined by inductively coupled plasma mass spectrometry on extracts from bulk samples after total acid digestion. Depth-wise profiles of {sup 206}Pb/{sup 207}Pb, {sup 206}Pb/{sup 204}Pb, {sup 207}Pb/{sup 204}Pb, {sup 208}Pb/{sup 204}Pb and {sup 208}Pb/{sup 207}Pb ratios showed, in general, an upward decrease for both intertidal and subtidal sediments as a consequence of the anthropogenic activities over the last century, or centuries. Waste channel samples from a nearby ceramic factory showed characteristic Pb stable isotope ratios different from those typical of coal and petrol. Natural isotope ratios from non-polluted samples were established for the study area, differentiating sediments from granitic or schist-gneiss sources. A binary mixing model employed on the polluted samples allowed estimating the anthropogenic inputs to the bay. These inputs represented between 25 and 98% of Pb inputs in intertidal samples, and 9-84% in subtidal samples, their contributions varying with time. Anthropogenic sources were apportioned according to a three-source model. Coal combustion-related emissions were the main anthropogenic source Pb to the bay (60-70%) before the establishment of the ceramic factory in the area (in the 1970s) which has since constituted the main source (95-100%), followed by petrol-related emissions. The Pb inputs history for the intertidal area was determined for the 20th century, and, for the subtidal area, the 19th and 20th centuries. -- Highlights: Black-Right-Pointing-Pointer Pb stable isotope ratios were applied to study Pb sources in coastal sediments. Black-Right-Pointing-Pointer Pb isotopic ratios were determined for pre-pollution and for industrial samples. Black

  10. Determination of lead, uranium, thorium, and thallium in silicate glass standard materials by isotope dilution mass spectrometry

    Science.gov (United States)

    Barnes, I.L.; Garner, E.L.; Gramlich, J.W.; Moore, L.J.; Murphy, T.J.; Machlan, L.A.; Shields, W.R.; Tatsumoto, M.; Knight, R.J.

    1973-01-01

    A set of four standard glasses has been prepared which have been doped with 61 different elements at the 500-, 50-, 1-, and 0.02-ppm level. The concentrations of lead, uranium, thorium, and thallium have been determined by isotope dilution mass spectrometry at a number of points in each of the glasses. The results obtained from independent determinations in two laboratories demonstrate the homogeneity of the samples and that precision of the order of 0.5% (95% L.E.) may be obtained by the method even at the 20-ppb level for these elements. The chemical and mass spectrometric procedures necessary are presented.

  11. Lead isotope signatures of Kerguelen plume-derived olivine-hosted melt inclusions: Constraints on the ocean island basalt petrogenesis

    Science.gov (United States)

    Borisova, Anastassia Y.; Faure, François; Deloule, Etienne; Grégoire, Michel; Béjina, Frédéric; de Parseval, Philippe; Devidal, Jean-Luc

    2014-06-01

    The nature of magmatic sources reflected by isotopic composition of the ocean island basalt (OIB) remains an on-going question in igneous geochemistry. To constrain the magmatic sources for OIB related to the Kerguelen plume activity, we performed detailed microanalytical investigation of the 21.4 Ma picritic basalt (MD109-D6-87) dredged during the “Marion Dufresne” cruise on a seamount between Kerguelen Archipelago and Heard Island. Lead isotope compositions of olivine-hosted melt inclusions and matrix glasses were measured by Laser Ablation Multiple Collector Inductively Coupled Plasma Mass Spectrometry (LA-MC-ICP-MS) and Secondary Ion Mass Spectrometry (SIMS). We also performed major and trace element microanalyses and mapping of the inclusions and the host olivine phenocrysts by electron microprobe (wavelength-dispersive X-ray spectroscopy, WDS). The observed significant major element (K2O/P2O5, Al2O3/TiO2) and Pb isotope (207Pb/206Pb and 208Pb/206Pb) heterogeneities of parental melts (MgO = 7-10 wt.%) during early high pressure crystallisation stage (200-300 MPa, Fo82-86 mol%), and relative homogeneity at later lower-pressure crystallisation stage ( 4), Al2O3/TiO2 (> 4) ratios are attributed to assimilation of the plateau basaltic crust (≥ 50 wt.%) by the melts in the magma chamber at palaeodepths from 6 to 9 km. The crustal assimilation may have happened through plagioclase dissolution. The large chemical and isotopic heterogeneity of the parental OIB melts found by in situ microanalyses in this study suggests that the bulk rock chemistry alone cannot provide enough information to constrain the nature of the magmatic sources.

  12. A rapid method for determination of the isotopic composition of uranium samples by alpha spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Martin Sanchez, A.; Tome, F.V.; Diaz Bejarano, J.; Jurado Vargas, M. (Dept. de Fisica, Univ. Extremadura, Badajoz (Spain))

    1992-03-01

    A simple method of analyzing alpha spectra from natural and enriched or depleted uranium samples is developed. The procedure is non-iterative, and takes into consideration low-energy tail and branching-ratio corrections to accurately calculate the area corresponding to each uranium isotope ({sup 234}U, {sup 235}U, {sup 236}U, {sup 238}U) in the spectrum, and then the isotopic composition of the sample. A BASIC computer program, called ENURA, has been developed to perform all the necessary calculations to give the results together with their uncertainties. Several samples were prepared with different uranium concentrations made from standard solutions with known compositions, and the method was checked against the experimental measurements from these samples. Other series of uranium spectra were theoretically constructed using a given line shape in order to cover the required range of enriched or depleted uranium. (orig.).

  13. Lead isotopes and the sources of the Columbia River Basalt Group

    Science.gov (United States)

    Chamberlain, V. E.; Lambert, R. St. J.

    1994-06-01

    A detailed study of Pb-208/Pb-204, Pb-207/Pb-204, and Pb-206/Pb-204 ratios suggests that the number of Pb isotopic reservoirs required for the Columbia River Basalt Group (CRBG) (as currently defined) must be increased from the presently accepted four to at least six. The identities of the six reservoirs are two of mid-ocean ridge basalt (MORB) slightly contaminated with sediment (R1 and R2, R1 being 'Cascades' PB); one a probable plume component (R3); two of unspecified mantle material but probably of R1 type, contaminated with local crustal Pb (R4 and R5); and the sixth a complex enriched reservoir of 2150 Ma age (R6). R1 is an end-member for all CRBG, except the Saddle Mountains Basalts. R2 is a second end-member for the Picture Gorge Basalt and CRBG, except the Saddle Mountains Basalts. R2 is a second end-member for the Picture Gorge Basalt and appears to be unique to it. R3 is the principal source for most of the Wanapum Basalt, as well as for most of the chemically evolved portions of the Grande Ronde Basalt. Volumetric and tectonic considerations require that one source of the CRBG be a plume or, at least, a nonlocal crustal or uppermost mantle source, and R3 is the ideal candidate for that role. R4 is the second source for the Imnaha Basalt, and R5 is the source for the (206)Pb-rich varieties of the Grande Ronde Basalt. R4 and R5 are identified with contamination by local Phanerozoic crust because of their similarity to local crustal Pb and because the rocks which contain them also have Cu contents correlated with their Pb isotopic compositions. R6 is the parent for Pb in all the Saddle Mountain Basalts. This last source appears to have been homogeneous 2150 m.y. ago but has since split into a number of separate, discrete pockets, each with its own characteristic Pb isotopic signature. Some of these appear in individual Saddle Mountain Basalt flows, while other sources have mixed with R4 to produce individual Saddle Mountain Basalt flows of the Ice Harbor

  14. RAPID DETERMINATION OF 237 NP AND PU ISOTOPES IN WATER BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY AND ALPHA SPECTROMETRY

    Energy Technology Data Exchange (ETDEWEB)

    Maxwell, S.; Jones, V.; Culligan, B.; Nichols, S.; Noyes, G.

    2010-06-23

    A new method that allows rapid preconcentration and separation of plutonium and neptunium in water samples was developed for the measurement of {sup 237}Np and Pu isotopes by inductively-coupled plasma mass spectrometry (ICP-MS) and alpha spectrometry; a hybrid approach. {sup 238}U can interfere with {sup 239}Pu measurement by ICP-MS as {sup 238}UH{sup +} mass overlap and {sup 237}Np via peak tailing. The method provide enhanced removal of uranium by separating Pu and Np initially on TEVA Resin, then moving Pu to DGA resin for additional removal of uranium. The decontamination factor for uranium from Pu is almost 100,000 and the decontamination factor for U from Np is greater than 10,000. This method uses stacked extraction chromatography cartridges and vacuum box technology to facilitate rapid separations. Preconcentration is performed using a streamlined calcium phosphate precipitation method. Purified solutions are split between ICP-MS and alpha spectrometry so that long and short-lived Pu isotopes can be measured successfully. The method allows for simultaneous extraction of 20 samples (including QC samples) in 4 to 6 hours, and can also be used for emergency response. {sup 239}Pu, {sup 242}Pu and {sup 237}Np were measured by ICP-MS, while {sup 236}Pu, {sup 238}Pu, and {sup 239}Pu were measured by alpha spectrometry.

  15. Pb isotope geochemistry of lead, zinc, gold and silver deposit clustered region, Liaodong rift zone,northeastern China

    Institute of Scientific and Technical Information of China (English)

    CHEN; Jiangfeng; YU; Gang; XUE; Chunji; QIAN; Hui; HE; Jian

    2005-01-01

    33 Pb isotopic analyses were reported for sulfide and hydrothermal carbonate minerals and marble of the Xiquegou lead-zinc, the Zhenzigou zinc-lead and the Gaojiapuzi silver deposits from the Qingchengzi ore field and the Beiwagou zinc-lead deposit in the west, Proterozoic Liaodong rift zone. Pb isotopic ratios of the marble from the Qingchengzi ore field range from 18.24 to 30.63 for 206Pb/204Pb, 15.59 to 17.05 for 207Pb/204Pb and 37.43 to 38.63 for 208Pb/204Pb. The marble gives a Pb-Pb isochron age of 1822±92 Ma, which is interpreted as the age of the metamorphism of the marble. Ore Pb, including Pb of sulfide and hydrothermal carbonate minerals, from the Qingchengzi ore field shows limited variation with 206Pb/204Pb=17.66-17.96, 207Pb/204Pb=15.60-15.74 and 208Pb/204Pb=37.94-38.60. In contrast, ore Pb from the Beiwagou deposit gives different Pb isotopic ratios with 206Pb/204Pb=15.68-15.81, 207Pb/204Pb= 15.34-15.45 and 208Pb/204Pb=35.30-35.68. Pb of all deposits from the Liaodong rift zone is derived from the upper crust. Ore Pb of the Qingchengzi deposits is derived from a young upper crust. The model Th/U ratios of 4.40 to 4.74 for ore Pb are significantly different from that of 1.7 to 4.4 given by the marble of the Qingchengzi ore field, suggesting that marble is not the source of the ore Pb. Ore Pb of the Beiwagou deposit is extracted from its source and the deposit is formed at the Paleoproterozoic era. Different Pb isotopic ratios of the Qingchengzi ore field and the Beiwagou deposit are due to different ages of the deposits and suggest that the two types of deposits are derived from different sources and are possibly formed by different ore-forming processes.

  16. [High-precision in situ analysis of the lead isotopic composition in copper using femtosecond laser ablation MC-ICP-MS and the application in ancient coins].

    Science.gov (United States)

    Chen, Kai-Yun; Fan, Chao; Yuan, Hong-Lin; Bao, Zhi-An; Zong, Chun-Lei; Dai, Meng-Ning; Ling, Xue; Yang, Ying

    2013-05-01

    In the present study we set up a femtosecond laser ablation MC-ICP-MS method for lead isotopic analysis. Pb isotopic composition of fifteen copper (brass, bronze) standard samples from the National Institute of Standards Material were analyzed using the solution method (MC-ICP-MS) and laser method (fLA-MC-ICPMS) respectively, the results showed that the Pb isotopic composition in CuPb12 (GBW02137) is very homogeneous, and can be used as external reference material for Pb isotopic in situ analysis. On CuPb12 112 fLA-MC-ICPMS Pb isotope analysis, the weighted average values of the Pb isotopic ratio are in good agreement with the results analyzed by bulk solution method within 2sigma error, the internal precision RSEs of the 208 Pb/204 Pb ratio and 207 Pb/206 Pb ratio are less than 90 and 40 ppm respectively, and the external precision RSDs of them are less than 60 and 30 ppm respectively. Pb isotope of thirteen ancient bronze coins was analyzed via fLA-MC-ICPMS, the results showed that the Pb isotopic composition of ancient coins of different dynasties is significantly different, and not all the Pb isotopic compositions in the coins even from the same dynasty are in agreement with each other.

  17. Lead

    Science.gov (United States)

    ... found? Who is at risk? What are the health effects of lead? Get educational material about lead Get certified as a Lead Abatement Worker, or other abatement discipline Lead in drinking water Lead air pollution Test your child Check and maintain your home ...

  18. Determination of lead, cadmium and thallium in water samples at ppb and ppt-levels by isotope dilution mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Trettenbach, J.; Heumann, K.G.

    1985-10-01

    An analytical procedure by isotope dilution mass spectrometry for the simultaneous determination of lead, cadmium and thallium traces in water samples down to the ppt-level is described. As a definitive method this type of analysis is especially advantageous to calibrate other analytical methods. A cathodic electrodeposition is used for the separation of the analysed heavy metals. A spike solution containing SWPb, WCd and STTl is applied for the isotope dilution technique. Positive thermal ions of the elements are successively measured by increasing the temperature of the filament in a single-filament ion source. The blank contribution of chemicals of different degree of purity for the analytical procedure was investigated. Different spring water samples dependent on the type of soil were analysed. Drinking water samples showed a significant difference in the heavy metal concentration dependent on the frequency in which the water-pipe was used. In this case, thallium is an especially sensitive indicator. It has been found for lead and cadmium that in contrast to thallium a high portion of both elements is fixed at small particles which can be included in the drinking water or is adsorbed at the surface of a quartz vessel. (orig.).

  19. Trace metal concentrations and lead isotopic composition in surface waters of the Northeast Pacific along the United States - Mexico boundary

    Energy Technology Data Exchange (ETDEWEB)

    Sanudo-Wilhelmy, S. (Inst. of Marine Science, Santa Cruz, CA (United States))

    1990-01-09

    To evaluate the magnitude of heavy metal contamination along the United States - Mexico boundary, trace metal concentrations (Pb, Cd, Mn, Fe, and Zn) and lead isotopic composition ([sup 204]Pb, [sup 206]Pb, [sup 207]Pb, and [sup 208]Pb) were measured along four surface water transects across the continental shelf off the Baja California Coast. The stations were located between 2 to 45 km offshore, including both coastal and open ocean locations. All the metal distributions along the transects were characterized by offshore concentration gradients. The highest trace metal concentrations occurred in coastal waters in association with high salinities and nutrient concentrations. There was also a longshore gradient in trace metal concentrations. Trace element concentrations were lower in the southern locations than along the United States - Mexico boundary, and were comparable to typical open ocean values. The relative enrichment of metals in surface waters off the northern part of Baja California was primarily associated with advection/upwelling processes, not with anthropogenic inputs. Mass balance calculations indicated that about 1% of Cd and 13% of Zn were from urban discharges. The low metal levels measured in coastal waters off the central part of Baja California were attributed to the intrusion of open ocean waters, based on hydrographic data, satellite images and lead isotopic compositions.

  20. Lead-isotopic, sulphur-isotopic, and trace-element studies of galena from the Silesian-Cracow Zn-Pb ores, polymetallic veins from the Gory Swietokrzyskie MTS, and the Myszkow porphyry copper deposit, Poland

    Science.gov (United States)

    Church, S.E.; Vaughn, R.B.; Gent, C.A.; Hopkins, R.T.

    1996-01-01

    Lead-isotopic data on galena samples collected from a paragenetically constrained suite of samples from the Silesian-Cracow ore district show no regional or paragenetically controlled lead-isotopic trends within the analytical reproducibility of the measurements. Furthermore, the new lead-isotopic data agree with previously reported lead-isotopic results (R. E. Zartman et al., 1979). Sulfur-isotopic analyses of ores from the Silesian-Cracow district as well as from vein ore from the Gory Swietokrzyskie Mts. and the Myszkow porphyry copper deposit, when coupled with trace-element data from the galena samples, clearly discriminate different hydrothermal ore-forming events. Lead-isotopic data from the Permian and Miocene evaporite deposits in Poland indicate that neither of these evaporite deposits were a source of metals for the Silesian-Cracow district ores. Furthermore, lead-isotopic data from these evaporite deposits and the shale residues from the Miocene halite samples indicate that the crustal evolution of lead in the central and western European platform in southern Poland followed normal crustal lead-isotopic growth, and that the isotopic composition of crustal lead had progressed beyond the lead-isotopic composition of lead in the Silesian-Cracow ores by Permian time. Thus, Mesozoic and Tertiary sedimentary flysch rocks can be eliminated as viable source rocks for the metals in the Silesian-Cracow Mississippi Valley-type (MVT) deposits. The uniformity of the isotopic composition of lead in the Silesian-Cracow ores, when coupled with the geologic evidence that mineralization must post-date Late Jurassic faulting (E. Gorecka, 1991), constrains the geochemical nature of the source region. The source of the metals is probably a well-mixed, multi-cycle molasse sequence of sedimentary rocks that contains little if any Precambrian metamorphic or granitic clasts (S. E. Church, R. B. Vaughn, 1992). If ore deposition was post Late Jurassic (about 150 m. y.) or later

  1. Eculizumab Therapy Leads to Rapid Resolution of Thrombocytopenia in Atypical Hemolytic Uremic Syndrome

    Directory of Open Access Journals (Sweden)

    Han-Mou Tsai

    2014-01-01

    Full Text Available Eculizumab is highly effective in controlling complement activation in patients with the atypical hemolytic uremic syndrome (aHUS. However, the course of responses to the treatment is not well understood. We reviewed the responses to eculizumab therapy for aHUS. The results show that, in patients with aHUS, eculizumab therapy, when not accompanied with concurrent plasma exchange therapy, led to steady increase in the platelet count and improvement in extra-renal complications within 3 days. By day 7, the platelet count was normal in 15 of 17 cases. The resolution of hemolytic anemia and improvement in renal function were less predictable and were not apparent for weeks to months in two patients. The swift response in the platelet counts was only observed in one of five cases who received concurrent plasma exchange therapy and was not observed in a case of TMA due to gemcitabine/carboplatin. In summary, eculizumab leads to rapid increase in the platelet counts and resolution of extrarenal symptoms in patients with aHUS. Concurrent plasma exchange greatly impedes the response of aHUS to eculizumab therapy. Eculizumab is ineffective for gemcitabine/carboplatin associated TMA.

  2. Effect of Water Vapor, Temperature, and Rapid Annealing on Formamidinium Lead Triiodide Perovskite Crystallization

    Energy Technology Data Exchange (ETDEWEB)

    Aguiar, Jeffery A.; Wozny, Sarah; Alkurd, Nooraldeen R.; Yang, Mengjin; Kovarik, Libor; Holesinger, Terry; Al-Jassim, Mowafak M.; Zhu, Kai; Zhou, Weilie; Berry, J. J.

    2016-07-08

    Perovskite-based solar cells are one of the emerging candidates for radically lower cost photovoltaics. Herein, we report on the synthesis and crystallization of organic-inorganic formamidinium lead triiodide perovskite films under controlled atmospheric and environmental conditions. Using in situ (scanning) transmission electron microscopy, we make observations of the crystallization process of these materials in nitrogen and oxygen gas with and without the presence of water vapor. Complementary planar samples were also fabricated in the presence of water vapor and characterized by in situ X-ray diffraction. Direct observations of the material structure and final morphology indicate that the exposure to water vapor results in a porous film that is metastable, regardless of the presence of argon, nitrogen, or oxygen. However, the optimal crystallization temperature of 175 °C is unperturbed across conditions. Rapid modulation about the annealing temperature of 175 °C in ±25 °C steps (150-200 °C) promotes crystallization and significantly improves the film morphology by overcoming the presence of impregnated water trapped in the material. Following this processing protocol, we demonstrate substantial growth to micron-size grains via observation inside of an environmentally controlled transmission electron microscope. Adapting this insight from our in situ microscopy, we are able to provide an informed materials protocol to control the structure and morphology of these organic-inorganic semiconductors, which is readily applicable to benchtop device growth strategies.

  3. Effect of Water Vapor, Temperature, and Rapid Annealing on Formamidinium Lead Triiodide Perovskite Crystallization

    Energy Technology Data Exchange (ETDEWEB)

    Aguiar, Jeffery A.; Wozny, Sarah; Alkurd, Nooraldeen R.; Yang, Mengjin; Kovarik, Libor; Holesinger, Terry G.; Al-Jassim, Mowafak; Zhu, Kai; Zhou, Weilie; Berry, Joseph J.

    2016-07-08

    Perovskite-based solar cells are one of the emerging candidates for radically lower cost photovoltaics. Herein, we report on the synthesis and crystallization of organic-inorganic formamidinium lead triiodide perovskite films under controlled atmospheric and environmental conditions. Using in situ (scanning) transmission electron microscopy, we make observations of the crystallization process of these materials in nitrogen and oxygen gas with and without the presence of water vapor. Complementary planar samples were also fabricated in the presence of water vapor and characterized by in situ X-ray diffraction. Direct observations of the material structure and final morphology indicate that the exposure to water vapor results in a porous film that is metastable, regardless of the presence of argon, nitrogen, or oxygen. However, the optimal crystallization temperature of 175 degrees C is unperturbed across conditions. Rapid modulation about the annealing temperature of 175 degrees C in +/-25 degrees C steps (150-200 degrees C) promotes crystallization and significantly improves the film morphology by overcoming the presence of impregnated water trapped in the material. Following this processing protocol, we demonstrate substantial growth to micron-size grains via observation inside of an environmentally controlled transmission electron microscope. Adapting this insight from our in situ microscopy, we are able to provide an informed materials protocol to control the structure and morphology of these organic-inorganic semiconductors, which is readily applicable to benchtop device growth strategies.

  4. Using Natural Stable Calcium Isotopes to Rapidly Assess Changes in Bone Mineral Balance Using a Bed Rest Model to Induce Bone Loss

    Science.gov (United States)

    Morgan, J. L. L.; Skulan, J. L.; Gordon, G. E.; Smith, Scott M.; Romaniello, S. J.; Anbar, A. D.

    2012-01-01

    Metabolic bone diseases like osteoporosis result from the disruption of normal bone mineral balance (BMB) resulting in bone loss. During spaceflight astronauts lose substantial bone. Bed rest provides an analog to simulate some of the effects of spaceflight; including bone and calcium loss and provides the opportunity to evaluate new methods to monitor BMB in healthy individuals undergoing environmentally induced-bone loss. Previous research showed that natural variations in the Ca isotope ratio occur because bone formation depletes soft tissue of light Ca isotopes while bone resorption releases that isotopically light Ca back into soft tissue (Skulan et al, 2007). Using a bed rest model, we demonstrate that the Ca isotope ratio of urine shifts in a direction consistent with bone loss after just 7 days of bed rest, long before detectable changes in bone mineral density (BMD) occur. The Ca isotope variations tracks changes observed in urinary N-teleopeptide, a bone resorption biomarker. Bone specific alkaline phosphatase, a bone formation biomarker, is unchanged. The established relationship between Ca isotopes and BMB can be used to quantitatively translate the changes in the Ca isotope ratio to changes in BMD using a simple mathematical model. This model predicts that subjects lost 0.25 0.07% ( SD) of their bone mass from day 7 to day 30 of bed rest. Given the rapid signal observed using Ca isotope measurements and the potential to quantitatively assess bone loss; this technique is well suited to study the short-term dynamics of bone metabolism.

  5. Historical lead isotope record of a sediment core from the Derwent River (Tasmania, Australia): A multiple source environment

    Energy Technology Data Exchange (ETDEWEB)

    Townsend, Ashley T., E-mail: Ashley.Townsend@utas.edu.au [Central Science Laboratory, University of Tasmania, Private Bag 74, Hobart, Tasmania 7001 (Australia); Seen, Andrew J. [School of Chemistry, University of Tasmania, Locked Bag 1371, Launceston, Tasmania 7250 (Australia)

    2012-05-01

    A 105 cm sediment core from the Derwent River (Tasmania, Australia) was collected in 2004 and was characterised considering both physical (loss on ignition at 550 Degree-Sign C and grain size) and chemical (Fe, Cu, Zn, Cd and Pb concentrations, Pb isotope ratios and {sup 210}Pb dating) properties. The core was analysed to (i) investigate the historical profiles of some important elements associated with the Risdon zinc refinery adjacent to the Derwent River, (ii) determine Pb isotopic signatures of sediment samples, and (iii) assess the veracity of Pb isotope ratios as indicators of contaminant Pb input. Extractable metal concentrations were (all values as mg kg{sup -1}, non-normalised for grain size) Fe: 20,000-35,000, Zn: 42-4500, Pb: 5-1090, Cu: 13-141, and Cd: 1-31; with a close correlation between Cu, Zn, Cd and Pb. Metal enrichment factors (normalised to Al) were Pb: 0.9-144, Zn: 0.8-93, Cd: 0.8-30, Cu: 0.8-8.9 and Fe: 0.9-1.3, confirming anthropogenic contributions of Cu, Zn, Pb and Cd to the sediments. The onset of metal contamination above background levels occurred at a depth between 43 and 49 cm, with maximum concentrations noted near 20 cm for Cu, Zn, Cd and Pb. Lead isotope ratios were determined in sediments using sector field ICP-MS, and were found to be 36.5-38.8, 16.5-18.7 and 1.07-1.20 for {sup 208}Pb/{sup 204}Pb, {sup 206}Pb/{sup 204}Pb and {sup 206}Pb/{sup 207}Pb ratios, respectively. Major Australian ores processed at the refinery over the previous {approx} 90 years include those from Broken Hill, Rosebery, Mt Isa, Elura, Hellyer and Century deposits. Anthropogenic impact by Pb with Broken Hill type isotopic ratio was initially evident in the core at 43-49 cm. The introduction of Rosebery and Elura ores to the refinery was also clearly noted. Pb isotope ratios further highlight that the Derwent River has been exposed to a greater impact by anthropogenic Pb in comparison to other major Tasmanian rivers, namely the Huon and Tamar. - Highlights

  6. Metal enrichment and lead isotope analysis for source apportionment in the urban dust and rural surface soil.

    Science.gov (United States)

    Yu, Yang; Li, Yingxia; Li, Ben; Shen, Zhenyao; Stenstrom, Michael K

    2016-09-01

    To understand the metal accumulation in the environment and identify its sources, 29 different metal contents and lead (Pb) isotope ratios were determined for 40 urban dust samples, 36 surface soil samples, and one river sediment sample collected in the municipality of Beijing, China. Results showed that cadmium, copper (Cu), mercury, Pb, antimony (Sb), and zinc demonstrated to be the typical urban contaminants and mostly influenced by the adjacent human activities with higher content to background ratios and SD values. Among the 29 metal elements investigated, Cu and Sb were found to be the most distinct elements that were highly affected by the developing level and congestion status of the cities with much higher contents in dust in more developed and congested cities. There was a relatively wider range of Pb isotope ratios of country surface soil than those of urban dust. The results of source identification based on Pb isotope ratios showed that coal combustion was the first largest Pb source and vehicle exhaust was the second largest source. The sum of them accounted for 74.6% mass proportion of overall Pb pollution on average. The surface soil sample collected at an iron mine had the highest (204)Pb/(206)Pb, (207)Pb/(206)Pb, and (208)Pb/(206)Pb ratios indicating ore had much higher ratios than other sources. The fine particle subsamples had higher (204)Pb/(206)Pb, (207)Pb/(206)Pb, and (208)Pb/(206)Pb ratios than the coarse particle subsamples indicating more anthropogenic sources of coal combustion and vehicle exhaust for fine particles and more background influence for coarse particles. These results help with pinpointing the major Pb sources and applying suitable measures for the target sources.

  7. Estimation of lead sources in a Japanese cedar ecosystem using stable isotope analysis

    Energy Technology Data Exchange (ETDEWEB)

    Itoh, Yuko [Forestry and Forest Products Research Institute, Matsunosato 1, Tsukuba, Ibaraki 305-8687 (Japan)]. E-mail: yuko106@ffpri.affrc.go.jp; Noguchi, Kyotaro [Forestry and Forest Products Research Institute, Matsunosato 1, Tsukuba, Ibaraki 305-8687 (Japan); Takahashi, Masamichi [Forestry and Forest Products Research Institute, Matsunosato 1, Tsukuba, Ibaraki 305-8687 (Japan); Okamoto, Toru [Forestry and Forest Products Research Institute, Matsunosato 1, Tsukuba, Ibaraki 305-8687 (Japan); Yoshinaga, Shuichiro [Forestry and Forest Products Research Institute, Matsunosato 1, Tsukuba, Ibaraki 305-8687 (Japan)

    2007-06-15

    Anthropogenic Pb affects the environment worldwide. To understand its effect on forest ecosystem, Pb isotope ratios were determined in precipitation, various components of vegetation, the forest floor, soil and parent material in a Japanese cedar (Cryptomeria japonica D. Don) forest stand. The average {sup 206}Pb/{sup 207}Pb ratio in bulk precipitation was 1.14 {+-} 0.01 (mean {+-} SD), whereas that in the subsoil (20-130 cm) was 1.18 {+-} 0.01. Intermediate ratios ranging from 1.15 to 1.16 were observed in the vegetation, the forest floor, and the surface soil (0-10 cm). Using the {sup 206}Pb/{sup 207}Pb ratios, the contribution of anthropogenic sources to Pb accumulated in the forest were estimated by the simple binary mixing model. Sixty-two percent of the Pb in the forest floor, 71% in the vegetation, and 55% in the surface soil (0-10 cm) originated from anthropogenic sources, but only 16% in the sub-surface soil (10-20 cm) was anthropogenic. These results suggest that internal Pb cycling occurs mainly between surface soil and vegetation in a Japanese cedar ecosystem, and that anthropogenic Pb strongly influences Pb cycling. Although the Japanese cedar ecosystem has a shallow forest floor, very little atmospherically derived Pb migrated downward over 10 cm in depth.

  8. Rapid, high-purity chemical separation of molybdenum from iron meteorites for isotopic analysis by using thermal ionization mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Qi-Lu; Masuda, Akimasa (Tokyo Univ. (Japan). Dept. of Chemistry)

    1992-05-01

    A chemical procedure has been developed, which combines both solvent extraction and anion exchange, so that microgram amounts of Mo can be cleanly, rapidly and efficiently separated from gram amounts of iron meteorites. Particular attention was directed to the complete separation of Mo from Zr and Ru. The isotopic abundance ratios of Mo can subsequently be determined with high accuracy by using thermal ionization mass spectrometry. The experiments indicate that the behaviour of Mo during solvent extraction and anion exchange is considerably different from that reported previously. In particular, it was found that there is a very narrow range of HCl concentrations within which it is possible to separate Mo from Fe by solvent extraction. The reproducibility and recovery of the method were examined by using inductively coupled plasma atomic emission spectrometry. (Author).

  9. Temporal evolution of lead isotope ratios in sediments of the Central Portuguese Margin: a fingerprint of human activities.

    Science.gov (United States)

    Mil-Homens, Mário; Caetano, Miguel; Costa, Ana M; Lebreiro, Susana; Richter, Thomas; de Stigter, Henko; Trancoso, Maria A; Brito, Pedro

    2013-09-15

    Stable Pb isotope ratios ((206)Pb/(207)Pb, (208)Pb/(206)Pb), (210)Pb, Pb, Al, Ca, Fe, Mn and Si concentrations were measured in 7 sediment cores from the west coast of the Iberian Peninsula to assess the Pb contamination throughout the last 200 years. Independently of their locations, all cores are characterized by increasing Pb/Al rends not related to grain-size changes. Conversely, decreasing trends of (206)Pb/(207)Pb were found towards the present. This tendency suggest a change in Pb sources reflecting an increased proportion derived from anthropogenic activities. The highest anthropogenic Pb inventories for sediments younger than 1950s were found in the two shallowest cores of Cascais and Lisboa submarine canyons, reflecting the proximity of the Tagus estuary. Lead isotope signatures also help demonstrate that sediments contaminated with Pb are not constrained to estuarine-coastal areas and upper parts of submarine canyons, but are also to transferred to a lesser extent to deeper parts of the Portuguese Margin. Copyright © 2013 Elsevier Ltd. All rights reserved.

  10. Preliminary lead isotope investigations of brine from the Red Sea, Galena from the Kingdom of Saudi Arabia, and galena from United Arab Republic (Egypt)

    Science.gov (United States)

    Delevaux, M.H.; Doe, B.R.; Brown, G.F.

    1967-01-01

    The isotopic composition of lead in Red Sea chloride brine containing 0.5 ppm Pb is found to be similar to that of some Cenozoic ore leads such as galena at Rabigh in Saudi Arabia that may have formed during mineralization accompanying Tertiary rifting. Bir Ranga galena in Miocene sediments from United Arab Republic (Egypt) is also isotopically similar to lead in Red Sea brine. The chlorine brine must be considered a possible mineralizing fluid. Lead isotopes show promise for use in mineral prospect evaluation in that galena from Samrah is isotopically similar to that from Mahd adh Dhahab, which has been the only ore producer in Saudi Arabia since 1945. Drilling at Samrah does indicate a possible economic mineralization. The lead isotope data coupled with available geologic knowledge and geochronometry are used to tentatively divide the ore prospects of the Kingdom of Saudi Arabia into relative categories of mineralization age. Two Mesozoic and Cenozoic mineralizations are distinguished on the basis of a 207Pb/204Pb difference; an early Paleozoic mineralization grouping is outlined; and a late Precambrian mineralization period is suggested. ?? 1967.

  11. Stable isotopes of lead and strontium as tracers of sources of airborne particulate matter in Kyrgyzstan.

    Science.gov (United States)

    Central Asia is dominated by an arid climate and desert-like conditions, leading to the potential of long-range transport of desert dust. One potential source of dust to Central Asia is the Aral Sea, the surface area of which has receded in size from 68,000 km2 to 14,280 km2, lar...

  12. Lead fluxes and 206Pb/207Pb isotope ratios in rime and snow collected at remote mountain-top locations (Czech Republic, Central Europe): Patterns and sources

    Science.gov (United States)

    Cimova, Nikoleta; Novak, Martin; Chrastny, Vladislav; Curik, Jan; Veselovsky, Frantisek; Blaha, Vladimir; Prechova, Eva; Pasava, Jan; Houskova, Marie; Bohdalkova, Leona; Stepanova, Marketa; Mikova, Jitka; Krachler, Michael; Komarek, Arnost

    2016-10-01

    During three winter seasons (2009-2011), Pb concentrations were measured in precipitation at 10 high-elevation sites in the Czech Republic, close to the borders with Austria, Germany, Poland, and Slovakia. Soluble and insoluble Pb forms were quantified in snow (vertical deposition), and rime (horizontal deposition). The objective was to compare Pb input fluxes into ecosystems via vertical and horizontal deposition, and to identify the residual Pb pollution sources in an era of rapidly decreasing industrial pollution. Lead soluble in diluted HNO3 made up 96% of total Pb deposition, with the remaining 4% Pb bound mainly in silicates. Three times higher concentrations of soluble Pb in rime than in snow, and 2.5 times higher concentrations of insoluble Pb in rime than in snow were associated with slightly different Pb isotope ratios. On average, the 206Pb/207Pb ratios in rime were higher than those in snow. Higher mean 206Pb/207Pb ratios of insoluble Pb (1.175) than in soluble Pb (1.165) may indicate an increasing role of geogenic Pb in recent atmospheric deposition. A distinct reversal to more radiogenic 206Pb/207Pb ratios in snow and rime in 2010, compared to literature data from rain-fed Sphagnum peatlands (1800-2000 A.D.), documented a recent decrease in anthropogenic Pb in the atmosphere of Central Europe. Since the early 1980s, Pb concentrations in snow decreased 18 times in the rural south of the Czech Republic, but only twice in the industrial north of the Czech Republic. Isotope signatures indicated that Pb in today's atmospheric deposition is mainly derived from Mesozoic ores mined/processed in Poland and coal combustion in the Czech Republic and Poland.

  13. Using lead isotopes and trace element records from two contrasting Lake Tanganyika sediment cores to assess watershed – Lake exchange

    Science.gov (United States)

    Odigie, Kingsley; Cohen, A.D.; Swarzenski, Peter W.; Flegal, R

    2014-01-01

    Lead isotopic and trace element records of two contrasting sediment cores were examined to reconstruct historic, industrial contaminant inputs to Lake Tanganyika, Africa. Observed fluxes of Co, Cu, Mn, Ni, Pb, and Zn in age-dated sediments collected from the lake varied both spatially and temporally over the past two to four centuries. The fluxes of trace elements were lower (up to 10-fold) at a mid-lake site (MC1) than at a nearshore site (LT-98-58), which is directly downstream from the Kahama and Nyasanga River watersheds and adjacent to the relatively pristine Gombe Stream National Park. Trace element fluxes at that nearshore site did not measurably change over the last two centuries (1815–1998), while the distal, mid-lake site exhibited substantial changes in the fluxes of trace elements – likely caused by changes in land use – over that period. For example, the flux of Pb increased by ∼300% from 1871 to 1991. That apparent accelerated weathering and detrital mobilization of lithogenic trace elements was further evidenced by (i) positive correlations (r = 0.77–0.99, p < 0.05) between the fluxes of Co, Cu, Mn, Ni, Pb, and Zn and those of iron (Fe) at both sites, (ii) positive correlations (r = 0.82–0.98, p < 0.01, n = 9) between the fluxes of elements (Al, Co, Cu, Fe, Mn, Ni, Pb, and Zn) and the mass accumulation rates at the offshore site, (iii) the low enrichment factors (EF < 5) of those trace elements, and (iv) the temporal consistencies of the isotopic composition of Pb in the sediment. These measurements indicate that accelerated weathering, rather than industrialization, accounts for most of the increases in trace element fluxes to Lake Tanganyika in spite of the development of mining and smelting operations within the lake’s watershed over the past century. The data also indicate that the mid-lake site is a much more sensitive and useful recorder of environmental changes than the nearshore site. Furthermore, the lead isotopic compositions

  14. Lead isotope ratios in six lake sediment cores from Japan Archipelago: Historical record of trans-boundary pollution sources

    Energy Technology Data Exchange (ETDEWEB)

    Hosono, Takahiro, E-mail: hosono@kumamoto-u.ac.jp [Priority Organization for Innovation and Excellence, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555 (Japan); Alvarez, Kelly [Priority Organization for Innovation and Excellence, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555 (Japan); Kuwae, Michinobu [Senior Research Fellow Center, Ehime University, 2-5 Bunkyo-cho, Matsuyama 790-8577 (Japan)

    2016-07-15

    Sediment cores from six lakes situated from north to south on the Japanese Archipelago were collected during 2009–2010 to investigate the hypothesis that deposition of lead (Pb) was coming from East Asia (including China, South Korea and eastern part of Russia). Accumulation rates and ages of the lake sediment were estimated by the {sup 210}Pb constant rate of supply model and {sup 137}Cs inputs to reconstruct the historical trends of Pb accumulation. Cores from four lakes located in the north and central Japan, showed clear evidence of Pb pollution with a change in the {sup 206}Pb/{sup 207}Pb and {sup 208}Pb/{sup 207}Pb ratios in the recent sediment as compared to the deeper sediment. Among the six studied lakes, significant inputs of anthropogenic lead emissions were observed at Lake Mikazuki (north Hokkaido in north Japan), Lake Chokai (north of Honshu), and Lake Mikuriga (central part of Honshu). Pb isotopic comparison of collected core sediment and previously reported data for wet precipitation and aerosols from different Asian regions indicate that, before 1900, Pb accumulated in these three lakes was not affected by trans-boundary sources. Lake Mikazuki started to receive Pb emissions from Russia in early 1900s, and during the last two decades, this lake has been affected by trans-boundary Pb pollution from northern China. Lake Chokai has received Pb pollutant from northern China since early 1900s until 2009, whereas for the Lake Mikuriga the major Pb contaminant was transported from southern China during the past 100 years. The results of our study demonstrate that Japan Archipelago has received trans-boundary Pb emissions from different parts of East Asian region depending on location, and the major source region has changed historically. - Highlights: • Historical trend of Pb pollution was recorded in six Japanese Lakes. • Pb concentration and Pb isotope ratios were determined for sediment cores. • High [Pb] and less radiogenic Pb isotope ratios

  15. Automated method for simultaneous lead and strontium isotopic analysis applied to rainwater samples and airborne particulate filters (PM10).

    Science.gov (United States)

    Beltrán, Blanca; Avivar, Jessica; Mola, Montserrat; Ferrer, Laura; Cerdà, Víctor; Leal, Luz O

    2013-09-03

    A new automated, sensitive, and fast system for the simultaneous online isolation and preconcentration of lead and strontium by sorption on a microcolumn packed with Sr-resin using an inductively coupled plasma mass spectrometry (ICP-MS) detector was developed, hyphenating lab-on-valve (LOV) and multisyringe flow injection analysis (MSFIA). Pb and Sr are directly retained on the sorbent column and eluted with a solution of 0.05 mol L(-1) ammonium oxalate. The detection limits achieved were 0.04 ng for lead and 0.03 ng for strontium. Mass calibration curves were used since the proposed system allows the use of different sample volumes for preconcentration. Mass linear working ranges were between 0.13 and 50 ng and 0.1 and 50 ng for lead and strontium, respectively. The repeatability of the method, expressed as RSD, was 2.1% and 2.7% for Pb and Sr, respectively. Environmental samples such as rainwater and airborne particulate (PM10) filters as well as a certified reference material SLRS-4 (river water) were satisfactorily analyzed obtaining recoveries between 90 and 110% for both elements. The main features of the LOV-MSFIA-ICP-MS system proposed are the capability to renew solid phase extraction at will in a fully automated way, the remarkable stability of the column which can be reused up to 160 times, and the potential to perform isotopic analysis.

  16. Rapid mass-spectrometric determination of boron isotopic distribution in boron carbide.

    Science.gov (United States)

    Rein, J E; Abernathey, R M

    1972-07-01

    Boron isotopic ratios are measured in boron carbide by thermionic ionization mass spectrometry with no prior chemical separation. A powder blend of boron carbide and sodium hydroxide is prepared, a small portion is transferred to a tantalum filament, the filament is heated to produce sodium borate, and the filament is transferred to the mass spectrometer where the(11)B/(10)B ratio is measured, using the Na(2)BO(2)(+) ion. Variables investigated for their effect on preferential volatilization of (10)B include the sodium hydroxide-boron carbide ratio and the temperature and duration of filament heating. A series of boron carbide pellets containing natural boron, of the type proposed for the control rods of the Fast Flux Test Facility reactor, were analysed with an apparently unbiased result of 4.0560 for the (11)B/(10)B ratio (standard deviation 0.0087). The pellets contained over 3% metal impurities typically found in this material. Time of analysis is 45 min per sample, with one analyst.

  17. High-resolution isotope measurements resolve rapid ecohydrological dynamics at the soil-plant interface.

    Science.gov (United States)

    Volkmann, Till H M; Haberer, Kristine; Gessler, Arthur; Weiler, Markus

    2016-05-01

    Plants rely primarily on rainfall infiltrating their root zones - a supply that is inherently variable, and fluctuations are predicted to increase on most of the Earth's surface. Yet, interrelationships between water availability and plant use on short timescales are difficult to quantify and remain poorly understood. To overcome previous methodological limitations, we coupled high-resolution in situ observations of stable isotopes in soil and transpiration water. We applied the approach along with Bayesian mixing modeling to track the fate of (2) H-labeled rain pulses following drought through soil and plants of deciduous tree ecosystems. We resolve how rainwater infiltrates the root zones in a nonequilibrium process and show that tree species differ in their ability to quickly acquire the newly available source. Sessile oak (Quercus petraea) adjusted root uptake to vertical water availability patterns under drought, but readjustment toward the rewetted topsoil was delayed. By contrast, European beech (Fagus sylvatica) readily utilized water from all soil depths independent of water depletion, enabling faster uptake of rainwater. Our results demonstrate that species-specific plasticity and responses to water supply fluctuations on short timescales can now be identified and must be considered to predict vegetation functional dynamics and water cycling under current and future climatic conditions.

  18. Lead isotope study of Zn-Pb ore deposits associated with the Basque-Cantabrian basin and Paleozoic basement, Northern Spain

    Science.gov (United States)

    Velasco, F.; Pesquera, A.; Herrero, J. M.

    1996-01-01

    A total of forty-three galena samples from syngenetic and epigenetic Pb-Zn mineralizations emplaced in the Lower Cretaceous Basque-Cantabrian basin and Paleozoic basement of the Cinco Villas massif in the western Pyrenees, have been analyzed for Pb-isotopic composition. Galena from sedex mineralizations hosted in Carboniferous clastic rocks in the Cinco Villas massif display an homogeneous lead isotopic signature (206Pb/2044Pb ≈ 18.43, 207Pb/204Pb ≈ 15.66, 208Pb/ 204Pb ≈ 38.69) suggesting a single lead reservoir. These values are slightly more radiogenic than lead from other European Hercynian deposits, possibly reflecting the influence of a more evolved upper crustal source. Underlying Paleozoic sediments are proposed as lead source for the Cinco Villas massif ores. Analyses from twenty-six galena samples from the four strata-bound ore districts hosted in Mesozoic rocks reveal the existence of two populations regarding their lead isotopic composition. Galena from the western Santander districts (e.g., Reocin) is characterized by more radiogenic isotope values (206Pb/204Pb ≈ 18.74, 207Pb/204Pb ≈ 15.67, 208Pb/ 204Pb ≈ 38.73) than those from the central and eastern districts (Troya-Legorreta, Central and Western Vizcaya, 206Pb/204Pb ≈ 18.59, 207Pb/204Pb ≈ 15.66, 208Pb/ 204Pb ≈ 38.73). In all districts, the most likely source for these mineralizations was the thick sequence of Lower Cretaceous clastic sediments. The existence of two separate lead isotopic populations could be the result of regional difference in the composition of the basement rocks and the clastic sediments derived of it or different evolution histories. In both sub-basins, isotopic ratios indicate an increase in crustal influence as the age of the ores decreases.

  19. Uranium-lead isotopic ages from the Sierra Nevada Batholith, California

    Science.gov (United States)

    Chen, James H.; Moore, James G.

    1982-06-01

    all in the range 99±3 m.y., indicating a relatively short period of emplacement and cooling for this nested group of plutons. U-Pb ages of a mafic inclusion and its host granodiorite indicate that both were derived from a common source or that the mafic inclusion was totally equilibrated with the granodioritic magma. Comparison of isotopic ages determined by different methods such as zircon U-Pb, sphene U-Pb, hornblende K-Ar, and biotite K-Ar suggests that zircon U-Pb ages generally approximate the emplacement age of a pluton. However, some plutons probably contain inherited or entrained old zircons, and the zircons of some samples are disturbed by younger thermal and metamorphic events. The ages reported here are consistent with U-Pb age determinations previously made on granitic rocks to the north [Stern et al., 1981], The age distribution of granitic belts determined here is in general agreement with those established by K-Ar dating [Evernden and Kistler, 1970] but does not differentiate the five epochs of plutonism determined in their study.

  20. Lead isotopes in soils and groundwaters as tracers of the impact of human activities on the surface environment: The Domizio-Flegreo Littoral (Italy) case study

    Science.gov (United States)

    Grezzi, G.; Ayuso, R.A.; de Vivo, B.; Lima, A.; Albanese, S.

    2011-01-01

    The isotopic signature of geogenic and anthropogenic materials, in combination with concentration data for pollutants, can help trace the origin and the extent of contamination in the environment. This approach is particularly effective if naturally occurring and anthropogenically introduced metals have different isotopic ratios. Lead isotope analysis on soils from 7 profiles (1. m depth) and on groundwaters from 8 wells have been used to determine the impact of human activities on the surface environment of Domizio-Flegreo Littoral. Result obtained show that in sub-rural areas the isotopic composition of the samples collected along the soil profiles of Domizio-Flegreo Littoral is likely mostly controlled by the nature of the parent geologic material (natural) while in more urbanized areas (Giugliano) Pb isotopic composition in superficial soils is mostly influenced by anthropic sources such as motor vehicles. Lead isotopic ratios in groundwaters also show that the use of pesticides and, probably, the influence of aerosols and the presence of illegal waste disposal can influence water quality. ?? 2010 Elsevier B.V.

  1. Rapid and simultaneous determination of neptunium and plutonium isotopes in environmental samples by extraction chromatography using sequential injection analysis and ICP-MS

    DEFF Research Database (Denmark)

    Qiao, Jixin; Hou, Xiaolin; Roos, Per

    2010-01-01

    This paper reports an automated analytical method for rapid and simultaneous determination of plutonium isotopes (239Pu and 240Pu) and neptunium (237Np) in environmental samples. An extraction chromatographic column packed with TrisKem TEVA® resin was incorporated in a sequential injection (SI...

  2. Proceedings of the XVIIth International Conference on Electromagnetic Isotope Separators and Related Topics (EMIS2015), Grand Rapids, MI, U.S.A., 11-15 May 2015

    Science.gov (United States)

    Bollen, Georg; Mittig, Wolfgang; Morrissey, Dave; Schwarz, Stefan; Villari, Antonio

    2016-06-01

    The 17th International Conference on Electromagnetic Isotope Separators and Related Topics (EMIS-2015) was held in Grand Rapids, Michigan, in the United States, from May 11th to 15th, 2015. The EMIS-2015 conference was hosted by Michigan State University. The present volume contains the proceedings of the event.

  3. Evidence for rapid climate change in North America during the latest Paleocene thermal maximum: oxygen isotope compositions of biogenic phosphate from the Bighorn Basin (Wyoming)

    Science.gov (United States)

    Fricke, Henry C.; Clyde, William C.; O'Neil, James R.; Gingerich, Philip D.

    1998-07-01

    Oxygen isotope records of Cenozoic sea water temperatures indicate that a rapid warming event known as the Latest Paleocene Thermal Maximum (LPTM) occurred during the otherwise gradual increase in world temperatures during the Late Paleocene and Early Eocene. Oxygen isotope analysis of the carbonate and phosphate components of hydroxyapatite found in mammalian tooth enamel and body scales of river-dwelling fish from the Bighorn Basin in Wyoming were made to investigate corresponding changes in the terrestrial climate. A comparison of carbonate and phosphate isotope data from modern and fossil material indicates that some diagenetic alteration of the fossil material has occurred, although systematically larger intra-tooth ranges in the oxygen isotope composition of carbonate indicate that it is more likely to have been affected than phosphate. Carbonate and phosphate from the ecologically diverse mammals and fishes both record a shift to higher oxygen isotope ratios at the same time and of the same duration as the LPTM. These shifts reflect a change in the isotopic composition of regional precipitation, which in turn provides the first evidence for continental climate change during the LPTM. Assuming the present-day relation between the oxygen isotope composition of precipitation and temperature applies to conditions in the past, and that animal physiology and behavior is relatively invariant over time, the isotopic shift is equivalent to an increase of surface temperature in western North America of several degrees. This result is consistent with the magnitude of high-latitude ocean warming, and provides a basis for relating marine and terrestrial oxygen isotope records to records of terrestrial biotic change.

  4. Lead

    Science.gov (United States)

    ... Chapter 6 Chapter 7 Chapter 8 Chapter 9 Appendix I Appendix II Tables Figures State Programs Alabama Alaska Arizona ... Tool Kit Resources Healthy Homes and Lead Poisoning Prevention Training Center (HHLPPTC) Training Tracks File Formats Help: ...

  5. Mineralogic, fluid inclusion, and sulfur isotope evidence for the genesis of Sechangi lead-zinc (-copper) deposit, Eastern Iran

    Science.gov (United States)

    Malekzadeh Shafaroudi, Azadeh; Karimpour, Mohammad Hassan

    2015-07-01

    The Sechangi lead-zinc (-copper) deposit lies in the Lut block metallogenic province of Eastern Iran. This deposit consists of ore-bearing vein emplaced along fault zone and hosted by Late Eocene monzonite porphyry. Hydrothermal alteration minerals developed in the wall rock include quartz, kaolinite, illite, and calcite. Microscopic studies reveal that the vein contains galena and sphalerite with minor chalcopyrite and pyrite as hypogene minerals and cerussite, anglesite, covellite, malachite, hematite, and goethite as secondary minerals. Fluorite and quartz are the dominant gangue minerals and show a close relationship with sulfide mineralization. Calculated δ34S values for the ore fluid vary between -9.9‰ and -5.9‰. Sulfur isotopic compositions suggest that the ore-forming aqueous solutions were derived from magmatic source and mixed with isotopically light sulfur, probably leached from the volcanic and plutonic country rocks. Microthermometric study of fluid inclusions indicates homogenization temperatures of 151-352 °C. Salinities of ore-forming fluids ranged from 0.2 to 16.5 wt.% NaCl equivalent. The ore-forming fluids of the Sechangi deposit are medium- to low-temperature and salinity. Fluid mixing may have played an important role during Pb-Zn (-Cu) mineralization. The key factors allowing for metal transport and precipitation during ore formation include the sourcing of magmatic fluids with high contents of metallogenic elements and the mixing of these hydrothermal fluids with meteoric waters resulting in the formation of deposit. In terms of the genetic type of deposit, the Sechangi is classified as a volcanic-subvolcanic hydrothermal-related vein deposit.

  6. Study on hydrogen isotopes permeation in fluidized state of liquid lithium-lead

    Energy Technology Data Exchange (ETDEWEB)

    Yoshimura, S.; Yoshimura, R.; Okada, M.; Fukada, S.; Edao, Y. [Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, Kasuga-shi, Fukuoka (Japan)

    2015-03-15

    Lithium-lead (Li-Pb) is one of the most promising candidate materials for the liquid blanket of fusion reactors. Hydrogen transfer under a fluidized condition of Li-Pb is investigated experimentally to design a Li-Pb blanket system. Li-Pb eutectic alloy flows inside a Ni tube in the experimental system, where H{sub 2} permeates into and out of the forced Li-Pb flow. The overall H{sub 2} permeation rate is analyzed using a mass balance model. Hydrogen atoms diffuse in Ni and Li-Pb. The steady-state H{sub 2} permeation rate obtained by this experiment is smaller than the result of the calculation model. A resistance factor is introduced to the present analysis in order to evaluate the influence of other H{sub 2} transfer mechanisms, such as diffusion in Li-Pb and dissolution reaction between Ni and Li-Pb. The contribution of the resistance to the overall H{sub 2} permeation rate becomes large when the flow rate of Li-Pb is low. This is because the boundary layer thickness between Ni and Li-Pb affects the overall H{sub 2} permeation rate. When the flow velocity of Li-Pb increases, the thickness of the boundary layer becomes thin, and the driving force of H{sub 2} permeation through the Ni wall becomes bigger. (authors)

  7. Metals and metalloids in atmospheric dust: Use of lead isotopic analysis for source apportionment

    Science.gov (United States)

    Felix Villar, Omar I.

    Mining activities generate aerosol in a wide range of sizes. Smelting activities produce mainly fine particles ( 1 microm). The adverse effects of aerosols on human health depend mainly on two key characteristics: size and chemical composition. One of the main objectives of this research is to analyze the size distribution of contaminants in aerosol produced by mining operations. For this purpose, a Micro-Orifice Uniform Deposit Impactor (MOUDI) was utilized. Results from the MOUDI samples show higher concentrations of the toxic elements like lead and arsenic in the fine fraction (Mitigation strategies could be developed if the source of contamination is well defined. Environmental conditions as wind speed, wind direction, relative humidity and precipitation have an important role in the concentration of atmospheric dust. Dry environments with low relative humidity are ideal for the transport of aerosols. Results obtained from this research show the relationship between dust concentrations and meteorological parameters. Dust concentrations are highly correlated with relative humidity and wind speed. With all the data collected on site and the analysis of the meteorological parameters, models can be develop to predict the transport of particles as well as the concentration of contaminants at a specific point. These models were developed and are part of the results shown in this dissertation.

  8. Sulfur- and lead-isotope signatures of orogenic gold mineralisation associated with the Hill End Trough, Lachlan Orogen, New South Wales, Australia

    Science.gov (United States)

    Downes, P. M.; Seccombe, P. K.; Carr, G. R.

    2008-11-01

    The Hill End Trough (HET) is a deformed middle Silurian to Early Devonian sediment-dominated rift within the northeastern Lachlan Orogen. The HET hosts the Hill End, Hargraves, Napoleon Reefs, Stuart Town and Windeyer low-sulfide orogenic gold deposits. Adjacent to the HET are the Bodangora and Gulgong gold deposits. In this study we present 91 new sulfur- and 18 new lead-isotope analyses and collate a further 25 sulfur- and 32 lead-isotopes analyses from unpublished sources for these deposits. Larger gold deposits in the HET have near 0 δ34S‰ values indicating that sulfur in these systems was sourced from a magmatic reservoir. The dominant lead isotope signature for HET-hosted deposits reflects a crustal source however some mantle-derived lead has been introduced into the HET. Sulfur- and lead-isotopic results suggest that gold was sourced from mantle-derived magmatic units beneath the HET. The study supports earlier studies at Hill End by concluding that the majority of orogenic gold mineralisation in and adjacent to the HET formed during the Early Carboniferous period.

  9. The effects of CaNa(2)EDTA on brain lead mobilization in rodents determined using a stable lead isotope tracer.

    Science.gov (United States)

    Seaton, C L; Lasman, J; Smith, D R

    1999-09-15

    Studies have demonstrated the efficacy of CaNa(2)EDTA for reducing lead (Pb) levels in blood and soft tissues, including brain. However, a concern remains that a single dose of CaNa(2)EDTA may cause a significant increase in brain Pb levels due to a redistribution of endogenous Pb. Here we utilized a rodent model of Pb exposure in combination with a sensitive stable Pb isotope tracer methodology to assess the effects of CaNa(2)EDTA chelation treatment on the redistribution of Pb in brain, blood, kidney, and bone tissues. Thirty-two adult female albino rats (n = 6-7 animals/group) were exposed to 100 microg Pb/mL in drinking water for 4 weeks. Stable (204)Pb tracer was administered via i.p. injection over 2 days prior to chelation. CaNa(2)EDTA was administered i.p. at a dose of 150 mg/kg/day for 1 to 5 days. Statistical differences were evaluated with univariate ANOVA. Under the Pb exposure and chelation treatment regimens utilized here, there was no evidence of a measurable redistribution of endogenous Pb (as total Pb or labile (204)Pb tracer) into the brain after a single CaNa(2)EDTA dose. Further, CaNa(2)EDTA was not efficacious in measurably reducing brain or bone Pb levels, although brain levels of labile (204)Pb tracer were significantly reduced after 5 days of chelation. CaNa(2)EDTA treatment was effective in significantly reducing both blood and kidney Pb levels. Overall, these data substantiate the efficacy of CaNa(2)EDTA for reducing soft tissue Pb levels, but not total brain Pb, and they do not support concern for a transient increase in brain Pb levels with treatment. Copyright 1999 Academic Press.

  10. Imperfect drug penetration leads to spatial monotherapy and rapid evolution of multidrug resistance

    NARCIS (Netherlands)

    Moreno-Gamez, Stefany; Hill, Alison L.; Rosenbloom, Daniel I. S.; Petrov, Dmitri A.; Nowak, Martin A.; Pennings, Pleuni S.

    2015-01-01

    Infections with rapidly evolving pathogens are often treated using combinations of drugs with different mechanisms of action. One of the major goal of combination therapy is to reduce the risk of drug resistance emerging during a patient's treatment. Although this strategy generally has significant

  11. Isotope Geochemistry of the Dongchuan Copper Deposit,Yunnan,SW China: Stratigraphic Chronology and Application of Lead Isotopes in Geochemical Exploration

    Institute of Scientific and Technical Information of China (English)

    常向阳; 朱炳泉

    2002-01-01

    In this paper the Pb-Pb isochron method was used to determine the isotopic ages of te Luoxue Formation dolomites(1716±56Ma),th Heishan Formation carbonaceous slated (1607±128Ma) of the middle sub-group of the Kunyang Group and the Dayingpan Formation carbonaceous slates(1258±Ma) of the upper sub-group of the Kunyang Group.The age of the middle sub-group of the Kunyang Group is about 1800-1600Ma,belonging to the Late Paleo-Proterozoic,and that of the Dayingpan Formation in the upper sub-group of the Kunyang Group is about 1200-1300Ma, belonging to the Middle Poroterozoic.In addition,the Pb isotope chemical exploration techniques were used to study systematically the Pb isotopic compositions of rocks and ores across the No.14 vein in the middle segment of the No.1 pit of the Tangdan copper deposit and the result showed that the Pb isotope V1 values are neatively correlated with the copper contents.In is the first trial to use the systematic section method to conduct Pb isotope chemical exploration.

  12. Isotope Geochemistry of the Dongchuan Copper Deposit, Yunnan, SW China:Stratigraphic Chronology and Application of Lead Isotopes in Geochemical Exploration

    Institute of Scientific and Technical Information of China (English)

    常向阳; 朱炳泉

    2002-01-01

    In this paper the Pb-Pb isochron method was used to determine the isotopic ages of the Luoxue Formation dolomites (1716 ± 56 Ma), the Heishan Formation carbonaceous slates(1607 ± 128 Ma) of the middle sub-group of the Kunyang Group and the Dayingpan Formation carbonaceous slates ( 1258 ± 70Ma) of the upper sub-group of the Kunyang Group. The age of the middle sub-group of the Kunyang Group is about 1800 - 1600 Ma, belonging to the Late Paleo-Proterozoic, and that of the Dayingpan Formation in the upper sub-group of the Kunyang Group is about 1200 - 1300 Ma, belonging to the Middle Proterozoic. In addition, the Pb isotope chemical exploration techniques were used to study systematically the Pb isotopic compositions of rocks and ores across the No. 14 vein in the middle segment of the No. 1 pit of the Tangdan copper deposit and the result showed that the Pb isotope V1 values are negatively correlated with the copper contents. It is the first trial to use the systematic section method to conduct Pb isotope chemical exploration.

  13. Coupling lead isotopes and element concentrations in epiphytic lichens to track sources of air emissions in the Alberta Oil Sands Region

    Science.gov (United States)

    A study was conducted that coupled use of element concentrations and lead (Pb) isotope ratios in the lichen Hypogymnia physodes collected during 2002 and 2008, to assess the impacts of air emissions from the Alberta Oil Sands Region (AOSR, Canada) mining and processing operations...

  14. Coupling lead isotopes and element concentrations in epiphytic lichens to track sources of air emissions in the Alberta Oil Sands Region

    Science.gov (United States)

    A study was conducted that coupled use of element concentrations and lead (Pb) isotope ratios in the lichen Hypogymnia physodes collected during 2002 and 2008, to assess the impacts of air emissions from the Alberta Oil Sands Region (AOSR, Canada) mining and processing operations...

  15. Carbon isotope ratios suggest no additional methane from boreal wetlands during the rapid Greenland Interstadial 21.2

    Science.gov (United States)

    Sperlich, Peter; Schaefer, Hinrich; Mikaloff Fletcher, Sara; Guillevic, Myriam; Lassey, Keith; Sapart, Célia; Röckmann, Thomas; Blunier, Thomas

    2017-04-01

    Samples from two Greenland ice cores (NEEM and NGRIP) have been measured for methane carbon isotope ratios (delta 13C-CH4) to investigate the CH4 mixing ratio anomaly during Greenland Interstadial (GI) 21.2 (85,000 years before present). This extraordinarily rapid event occurred within 150 years, comprising a CH4 mixing ratio pulse of 150 ppb (˜25%). Our new measurements disclose a concomitant shift in delta 13C-CH4 of 1‰ . Keeling plot analyses reveal the delta 13C of the additional CH4 source constituting the CH4 anomaly as -56.8 ± 2.8‰ , which we confirm by means of a previously published box model. We propose tropical wetlands as the most probable additional CH4 source during GI-21.2 and present independent evidence that suggests that tropical wetlands in South America and Asia have played a key role. We find no evidence that boreal CH4 sources, such as permafrost degradation, contributed significantly to the atmospheric CH4 increase, despite the pronounced warming in the Northern Hemisphere during GI-21.2.

  16. Rapid determination of parabens in personal care products by stable isotope GC-MS/MS with dynamic selected reaction monitoring.

    Science.gov (United States)

    Wang, Perry G; Zhou, Wanlong

    2013-06-01

    In this study, a rapid and sensitive analytical method for the determination of methyl-, ethyl-, propyl-, and butyl esters of para-hydroxy benzoic acid (parabens) in personal care products was developed and fully validated. Test portions were extracted with methanol followed by vortexing, sonication, centrifugation, and filtration without derivatization. The four parabens were quantified by GC-MS/MS in the electron ionization mode. Four corresponding isotopically labeled parabens were selected as internal standards, which were added at the beginning of the sample preparation and used to correct for recovery and matrix effects. Sensitivity, extraction efficiency, and recovery of the respective analytes were evaluated. The coefficients of determination (r(2)) were all greater than 0.995 for the four parabens investigated. The recoveries ranged from 97 to 107% at three spiked levels and a one-time (single) extraction efficiency greater than 97% was obtained. This method has been applied to screen 26 personal care products. This is the first time that a unique GC-MS/MS method with dynamic selected reaction monitoring and confirmation of analytes has been used to determine these parabens in cosmetic personal care products.

  17. Lead isotope exchange between dissolved and fluvial particulate matter: a laboratory study from the Johor River estuary

    Science.gov (United States)

    Chen, Mengli; Boyle, Edward A.; Lee, Jong-Mi; Nurhati, Intan; Zurbrick, Cheryl; Switzer, Adam D.; Carrasco, Gonzalo

    2016-11-01

    Atmospheric aerosols are the dominant source of Pb to the modern marine environment, and as a result, in most regions of the ocean the Pb isotopic composition of dissolved Pb in the surface ocean (and in corals) matches that of the regional aerosols. In the Singapore Strait, however, there is a large offset between seawater dissolved and coral Pb isotopes and that of the regional aerosols. We propose that this difference results from isotope exchange between dissolved Pb supplied by anthropogenic aerosol deposition and adsorbed natural crustal Pb on weathered particles delivered to the ocean by coastal rivers. To investigate this issue, Pb isotope exchange was assessed through a closed-system exchange experiment using estuarine waters collected at the Johor River mouth (which discharges to the Singapore Strait). During the experiment, a known amount of dissolved Pb with the isotopic composition of NBS-981 (206Pb/207Pb = 1.093) was spiked into the unfiltered Johor water (dissolved and particulate 206Pb/207Pb = 1.199) and the changing isotopic composition of the dissolved Pb was monitored. The mixing ratio of the estuarine and spike Pb should have produced a dissolved 206Pb/207Pb isotopic composition of 1.161, but within a week, the 206Pb/207Pb in the water increased to 1.190 and continued to increase to 1.197 during the next two months without significant changes of the dissolved Pb concentration. The kinetics of isotope exchange was assessed using a simple Kd model, which assumes multiple sub-reservoirs within the particulate matter with different exchange rate constants. The Kd model reproduced 56% of the observed Pb isotope variance. Both the closed-system experiment and field measurements imply that isotope exchange can be an important mechanism for controlling Pb and Pb isotopes in coastal waters. A similar process may occur for other trace elements. This article is part of the themed issue 'Biological and climatic impacts of ocean trace element chemistry'.

  18. Collateral damage: rapid exposure-induced evolution of pesticide resistance leads to increased susceptibility to parasites.

    Science.gov (United States)

    Jansen, Mieke; Stoks, Robby; Coors, Anja; van Doorslaer, Wendy; de Meester, Luc

    2011-09-01

    Although natural populations may evolve resistance to anthropogenic stressors such as pollutants, this evolved resistance may carry costs. Using an experimental evolution approach, we exposed different Daphnia magna populations in outdoor containers to the carbamate pesticide carbaryl and control conditions, and assessed the resulting populations for both their resistance to carbaryl as well as their susceptibility to infection by the widespread bacterial microparasite Pasteuria ramosa. Our results show that carbaryl selection led to rapid evolution of carbaryl resistance with seemingly no cost when assessed in a benign environment. However, carbaryl-resistant populations were more susceptible to parasite infection than control populations. Exposure to both stressors reveals a synergistic effect on sterilization rate by P. ramosa, but this synergism did not evolve under pesticide selection. Assessing costs of rapid adaptive evolution to anthropogenic stress in a semi-natural context may be crucial to avoid too optimistic predictions for the fitness of the evolving populations. © 2011 The Author(s).

  19. Isotopic signatures suggest important contributions from recycled gasoline, road dust and non-exhaust traffic sources for copper, zinc and lead in PM10 in London, United Kingdom

    Science.gov (United States)

    Dong, Shuofei; Ochoa Gonzalez, Raquel; Harrison, Roy M.; Green, David; North, Robin; Fowler, Geoff; Weiss, Dominik

    2017-09-01

    The aim of this study was to improve our understanding of what controls the isotope composition of Cu, Zn and Pb in particulate matter (PM) in the urban environment and to develop these isotope systems as possible source tracers. To this end, isotope ratios (Cu, Zn and Pb) and trace element concentrations (Fe, Al, Cu, Zn, Sb, Ba, Pb, Cr, Ni and V) were determined in PM10 collected at two road sites with contrasting traffic densities in central London, UK, during two weeks in summer 2010, and in potential sources, including non-combustion traffic emissions (tires and brakes), road furniture (road paint, manhole cover and road tarmac surface) and road dust. Iron, Ba and Sb were used as proxies for emissions derived from brake pads, and Ni, and V for emissions derived from fossil fuel oil. The isotopic composition of Pb (expressed using 206Pb/207Pb) ranged between 1.1137 and 1.1364. The isotope ratios of Cu and Zn expressed as δ65CuNIST976 and δ66ZnLyon ranged between -0.01‰ and +0.51‰ and between -0.21‰ and +0.33‰, respectively. We did not find significant differences in the isotope signatures in PM10 over the two weeks sampling period and between the two sites, suggesting similar sources for each metal at both sites despite their different traffic densities. The stable isotope composition of Pb suggests significant contribution from road dust resuspension and from recycled leaded gasoline. The Cu and Zn isotope signatures of tires, brakes and road dust overlap with those of PM10. The correlation between the enrichments of Sb, Cu, Ba and Fe in PM10 support the previously established hypothesis that Cu isotope ratios are controlled by non-exhaust traffic emission sources in urban environments (Ochoa Gonzalez et al., 2016). Analysis of the Zn isotope signatures in PM10 and possible sources at the two sites suggests significant contribution from tire wear. However, temporary additional sources, likely high temperature industrial emissions, need to be invoked

  20. Lead isotopic compositions of soil and near-surface till profiles from a watershed containing arsenic-enriched groundwater in coastal Maine

    Science.gov (United States)

    Ayuso, Robert; Foley, Nora; Wandless, Gregory; Dillingham, Jeremy; Colvin, Anna

    2005-01-01

    Lead isotope compositions of soils and near-surface tills from an area of coastal Maine known to have groundwater with anomalously high arsenic contents were measured in order to determine the source of the lead and, by inference, possible sources of arsenic. Five soil and till sites were selected for detailed chemical and isotopic analysis. To construct profiles of the soil and till horizons, five samples were collected at 10-cm intervals from the surface to the base of each horizon. Total lead and arsenic concentrations and lead isotopic compositions were measured for 48 leaches and bulk residues. The soils and tills are underlain by sulfidic schists of the Penobscot Formation. Several generations of minerals containing arsenic and lead exist in the regional bedrock, including rock-forming silicates (feldspar and micas), sulfide minerals formed during diagenesis (for example, arsenic-rich pyrite), and sulfide and oxide minerals that formed as a result of Silurian metamorphic and igneous events (for example, arsenopyrite, galena, iron-oxides, and arsenic-sulfides). A young group of secondary minerals (for example, iron-hydroxides, arsenic-hydroxides, lead-sulfate, and arsenic-jarosite) formed from recent weathering and pedogenic processes.

  1. Effects of rapid solidification on the microstructure and microhardness of a lead-free Sn-3.5Ag solder

    Institute of Scientific and Technical Information of China (English)

    SHEN Jun; LIU Yongchang; Han Yajing; GAO Houxiu

    2006-01-01

    A lead-free Sn-3.5Ag solder was prepared by rapid solidification technology. The high solidification rate, obtained by rapid cooling, promotes nucleation, and suppresses the growth of Ag3Sn intermetallic compounds (IMCs) in Ag-rich zone, yielding fine Ag3Sn nanoparticulates with spherical morphology in the matrix of the solder. The large amount of tough homogeneously-dispersed IMCs helps to improve the surface area per unit volume and obstructs the dislocation lines passing through the solder, which fits with the dispersion-strengthening theory. Hence, the rapidly-solidified Sn-3.5Ag solder exhibits a higher microhardness when compared with a slowly-solidified Sn-3.5Ag solder.

  2. Precision mass measurements for studies of nucleosynthesis via the rapid neutron-capture process. Penning-trap mass measurements of neutron-rich cadmium and caesium isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Atanasov, Dinko

    2016-07-06

    Although the theory for the rapid neutron-capture process (r-process) was developed more than 55 years ago, the astrophysical site is still under a debate. Theoretical studies predict that the r-process path proceeds through very neutron-rich nuclei with very asymmetric proton-to-neutron ratios. Knowledge about the properties of neutron-rich isotopes found in similar regions of the nuclear chart and furthermore suitable for r-process studies is still little or even not existing. The basic nuclear properties such as binding energies, half-lives, neutron-induced or neutron-capture reaction cross-sections, play an important role in theoretical simulations and can vary or even drastically alternate results of these studies. Therefore, a considerable effort was put forward to access neutron-rich isotopes at radioactive ion-beam facilities like ISOLDE at CERN. The goal of this PhD thesis is to describe the experimental work done for the precision mass measurements of neutron-rich cadmium ({sup 129-131}Cd) and caesium ({sup 132,146-148}Cs) isotopes. Measurements were done at the on-line radioactive ion-beam facility ISOLDE by using the four-trap mass spectrometer ISOLTRAP. The cadmium isotopes are key nuclides for the synthesis of stable isotopes around the mass peak A = 130 in the Solar System abundance.

  3. Lead isotopic signatures in Antarctic marine sediment cores: a comparison between 1M HCl partial extraction and HF total digestion pre-treatments for discerning anthropogenic inputs.

    Science.gov (United States)

    Townsend, A T; Snape, I; Palmer, A S; Seen, A J

    2009-12-20

    Sensitive analytical techniques are typically required when dealing with samples from Antarctica as even low concentrations of contaminants can have detrimental environmental effects. Magnetic Sector ICP-MS is an ideal technique for environmental assessment as it offers high sensitivity, multi-element capability and the opportunity to determine isotope ratios. Here we consider the Pb isotope record of five marine sediment cores collected from three sites in the Windmill Islands area of East Antarctica: Brown Bay adjacent to the current Australian station Casey, Wilkes near the abandoned US/Australian Station and McGrady Cove lying midway between the two. Two sediment pre-treatment approaches were considered, namely partial extraction with 1M HCl and total dissolution involving HF. Lead isotope ratio measurements made following sediment partial extraction provided a more sensitive indication of Pb contamination than either Pb concentrations alone (irrespective of sample pre-treatment method) or isotope ratios made after HF digestion, offering greater opportunity for discrimination between impacted and natural/geogenic samples and sites. Over 90% of the easily extractable Pb from sediments near Casey was anthropogenic in origin, consisting of Pb from major Australian deposits. At Wilkes impact from discarded batteries with a unique isotopic signature was found to be a key source of Pb contamination to the marine environment with ~70-80% of Pb being anthropogenic in origin. The country and source of origin of these batteries remain unknown. Little evidence was found suggesting contamination at Wilkes by Pb originating from the major US source, Missouri. No definitive assessment could be made regarding Pb impact at McGrady Cove as the collected sediment core was of insufficient depth. Although Pb isotope ratio signatures may indicate anthropogenic input, spatial concentration gradients at nearby Brown Bay suggest contamination at McGrady Cove is unlikely. We recommend

  4. Total lead (Pb) concentration in oil shale ash samples based on correlation to isotope Pb-210 gamma-spectrometric measurements

    Energy Technology Data Exchange (ETDEWEB)

    Vaasma, T.; Kiisk, M.; Tkaczyk, A.H. [University of Tartu (Estonia); Bitjukova, L. [Tallinn University of Technology (Estonia)

    2014-07-01

    (PF) and circulating fluidized bed (CFB) firing technology. These samples were analyzed to determine macro and trace elements by the ICP-MS method. The same samples were also measured with a high-purity germanium detector (planar BSI GPD-50400) to determine the activity concentrations of natural radionuclides. The lead concentrations and Pb-210 activity concentrations were determined, and the correlation between the corresponding values was analyzed. Initial results demonstrate a strong positive linear relationship between these values, with the coefficient of determination (R{sup 2}) over 94. The correlation coefficient (Pearson's, 'r') had a value over 0.95. Both Pb and Pb-210 values had an increasing trend from the bottom ash towards electrostatic precipitator (ESP) ashes. The strong linear correlation between Pb concentrations and Pb-210 activity concentrations gives a credible indication that lead can be measured in ash samples using its radioactive isotope Pb-210. Especially in situations where there are higher concentrations of Pb, for example in the case of wastes from the metallurgic and energy industries, this method could be used to detect the lead concentration quickly and with no chemical processing of the sample. Document available in abstract form only. (authors)

  5. Lead isotopic composition of trinitite melt glass: evidence for the presence of Canadian industrial lead in the first atomic weapon test.

    Science.gov (United States)

    Bellucci, Jeremy J; Simonetti, Antonio; Wallace, Christine; Koeman, Elizabeth C; Burns, Peter C

    2013-08-06

    The Pb isotopic compositions for 51 spots of melt glass in 11 samples of trinitite have been determined by laser ablation multicollector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS). Trinitite glass yields a large range of Pb isotopic compositions (i.e., (206)Pb/(204)Pb = 17.08-19.04), which reflect mixing between industrial Pb from materials used in the Trinity test and natural geologic components. Areas within trinitite melt glass containing high concentrations of both Cu and Pb, which are derived from the bomb and blast site-related components, were used for delineating the Pb isotopic composition corresponding to the anthropogenic Pb component. Comparison between the isotopic composition estimated here for the industrial Pb used in the Trinity test and those from known Pb deposits worldwide indicates close agreement with ore from the Buchans mine (Newfoundland, Canada). The Buchans mine was active during the time of the Trinity test and was operated by the American Smelting and Refining Company, which could have provided the Pb used in the test. The industrial Pb used in the Trinity test materials is not documented in the literature (or declassified) but could have been present in bricks, solder, pigs, or some other anthropogenic component related to the experiment.

  6. Rapid Diagnosis of Nonconvulsive Status Epilepticus Using Reduced-Lead Electroencephalography

    Directory of Open Access Journals (Sweden)

    Brenner, Jay M.

    2015-05-01

    Full Text Available Introduction: Electroencephalography (EEG is indicated for diagnosing nonconvulsive status epilepticus (NCSE in a patient who has altered level of consciousness after a motor seizure. A study in a neonatal population found 94% sensitivity and 78% specificity for detection of seizure using a single-lead device. This study aims to show that a reduced montage EEG would detect 90% of seizures detected on standard EEG. Methods: A portable Brainmaster EEG device was available in the emergency department (ED at all times. Patients presenting to the ED with altered mental status and known history of seizure or a witnessed seizure having a standard EEG were eligible for this study. The emergency physician obtained informed consent from the legally authorized representative (LAR, while an ED technician attached the electrodes to the patient, and a research associate attached the electrodes to the wiring routing to the portable EEG module. A board-certified epileptologist interpreted the tracings via the Internet. Simultaneously, the emergency physician ordered a standard 23-lead EEG, which would be interpreted by the neurologist on call to read EEGs. We compared the epileptologist’s interpretation of the reduced montage EEG to the results of the 23-lead EEG, which was considered the gold standard for detecting seizures. Results: Twelve of 12 patients or 100% had the same findings on reduced-montage EEG as standard EEG. One of 12 patients or 8% had nonconvulsive seizure activity. Conclusion: The results are consistent with prior studies which have shown that 8-48% of patients who have had a motor seizure continue to have nonconvulsive seizure activity on EEG. This study suggests that a bedside reduced-montage EEG can be used to make the diagnosis of NCSE in the ED. Further study will be conducted to see if this technology can be applied to the inpatient neurological intensive care unit setting. [West J Emerg Med. 2015;16(3:442–446.

  7. Lead isotope distribution in podzolic soil profiles on different types of bedrock in a formerly glaciated terrain (Oslo, Norway)

    Energy Technology Data Exchange (ETDEWEB)

    Saether, O.M., E-mail: ola.sather@ngu.no [Geological Survey of Norway, Leiv Eirikssons vei 39, NO-7094 Trondheim (Norway); Aberg, G. [Laboratory for Isotope Geology, Box 50007, SE-104 05 Stockholm (Sweden); Steinnes, E. [Department of Chemistry, NTNU, NO-7491 Trondheim (Norway)

    2011-06-15

    Highlights: > Four sites with different lithology (syenite, gneiss, granite, sedimentary rocks), formerly glaciated terrain, Oslo, Norway. > Variations with depth of grain-size, total organic C, Pb concentration, Pb isotope ratio. > Content of anthropogenic Pb in podzolic forest soil. > Comparison of three methods for calculating anthropogenic Pb input. > Amounts of anthropogenic Pb in upper 20 cm calculated to be 1-6 t/km{sup 2}. - Abstract: Lead has been exploited by man over thousands of years for a variety of metallurgical, medicinal, and industrial purposes. The cumulative output of Pb from mining is estimated to be 260 million metric tonnes and 85% of this has occurred over the last two centuries. Global annual production of Pb from mining was about 3 million tonnes at the turn of the millenium. Terrestrial ecosystems all over Norway have been contaminated moderately to strongly by Pb and other trace elements from atmospheric deposition. With the aim of developing a method for mapping the accumulated content of anthropogenic Pb and how deep in the soil profile the atmospherically deposited Pb has penetrated, the concentration of Pb and the {sup 206}Pb/{sup 207}Pb ratio has been studied in podzolic forest soils at four locations with different lithology, i.e. age and type of bedrock, in the Oslo area. The concentrations of Pb in the soil profiles are 6.6-38.1 mg/kg (median 10.3). The {sup 206}Pb/{sup 207}Pb ratio ranges between 1.168 and 1.314 (median 1.267) over the entire profile. In the upper 5 cm the range is 1.168-1.191, similar to ratios determined in recent atmospheric deposition. Applying three different methods, the amount of anthropogenically deposited Pb is estimated at 1-6 t/km{sup 2}.

  8. Morphology and microstructure of rapidly solidified tin-lead alloy powders

    Institute of Scientific and Technical Information of China (English)

    Xiang Qingchun; Zhang Wei; Qiu Keqiang; Qu Yingdong; Li Rongde

    2014-01-01

    Sn60Pb40 al oy powders were fabricated using the planar flow casting (PFC) atomization process. By using OM, SEM and EPMA, the characteristics of the morphologies and microstructures of the powders have been investigated. It is observed that the environment of ambient gas in the atomization box has great effects on the morphology of the al oy powders. The microstructures of Sn60Pb40 al oy powders produced by the PFC atomization process are completely composed of eutectic, which is made up of both oversaturated αsolid solution and β solid solution. The microstructures of smal size powders are extraordinarily undeveloped dendritic eutectic, in which the large majority of the α phase appears nearly spherical, evidently since the cooling rate is higher and the under-cooling is larger. As for the large size powders, since the cooling rate and undercooling are relatively low, lamel ar α phase apparently increases in the eutectic microstructures of these powders, and there is even typical lamellar eutectic structure clearly observed in some micro-areas. After remelting tests by DTA, the microstructures of smal size powders are transformed, which become composed of large crumby α phase and eutectic (α+β), while those of large size powders change into classical tin-lead structures of primary α phase plus lamellar eutectic (α+β). By studying the microstructures of tin-lead alloy powders, a model has been proposed to predict the microstructure formation of Sn60Pb40 al oy powders.

  9. Rapid economic growth leads to boost in NO2 pollution over India, as seen from space

    Science.gov (United States)

    Hilboll, Andreas; Richter, Andreas; Burrows, John P.

    2016-04-01

    Over the past decades, the Indian economy has been growing at an exceptional pace. This growth was induced and accompanied by a strong increase of the Indian population. Consequently, traffic, electricity consumption, and industrial production have soared over the past decades, leading to a strong increase in fuel consumption and thus pollutant emissions. Nitrogen oxides (NO+NO2) are a major component of anthropogenic air pollution, playing key part in reaction cycles leading to the formation of tropospheric ozone. They are mainly emitted by the combustion of fossil fuels; other sources include production by lightning, biomass burning, and microbial activity in soils. Since the mid-1990s, space-borne measurements of tropospheric nitrogen dioxide (NO2) have been conducted by the GOME, SCIAMACHY, GOME-2, and OMI instruments. These instruments perform hyperspectral measurements of scattered and reflected sunlight. Their measurements are then analyzed using differential optical absorption spectroscopy (DOAS) to yield vertically integrated columnar trace gas abundances. Here, we will present the results of 20 years of NO2 measurements over the Indian subcontinent. After showing the spatial distribution of NO2 pollution over India, we will present time series for individual states and urban agglomerations. These time series will then be related to various indicators of economic development. Finally, we will highlight several instances where single industrial pollution sources and their development can clearly be identified from the NO2 maps and estimate their NO2 emissions.

  10. 我国城市大气颗粒物的铅同位素丰度比%Lead Isotope Abundance Ratios of Urban Atmospheric Aerosols in China

    Institute of Scientific and Technical Information of China (English)

    刘咸德; 李显芳; 李冰

    2004-01-01

    Determined with ICP-MS, new isotope abundance ratio data of lead for Beijing and Changdao aerosols was presented, in comparison with literature data for Chinese urban aerosols. 206Pb/207Pb ratio falls into a range from 1.13 to 1.18 for urban aerosols and less influenced by vehicle exhaust emission after phase-out of leaded petrol in 2000 in China. Major lead pollution sources may probably include coal combustion, oil combustion,re-suspended dust, metallurgical industry and use and production of cement.

  11. Anthropogenic-driven rapid shifts in tree distribution lead to increased dominance of broadleaf species.

    Science.gov (United States)

    Vayreda, Jordi; Martinez-Vilalta, Jordi; Gracia, Marc; Canadell, Josep G; Retana, Javier

    2016-12-01

    Over the past century, major shifts in the geographic distribution of tree species have occurred in response to changes in land use and climate. We analyse species distribution and abundance from about 33 000 forest inventory plots in Spain sampled twice over a period of 10-12 years. We show a dominance of range contraction (extinction), and demographic decline over range expansion (colonization), with seven of 11 species exhibiting extinction downhill of their distribution. Contrary to expectations, these dynamics are not always consistent with climate warming over the study period, but result from legacies in forest structure due to past land use change and fire occurrence. We find that these changes have led to the expansion of broadleaf species (i.e. family Fagaceae) over areas formerly dominated by conifer species (i.e. family Pinaceae), due to the greater capacity of the former to respond to most disturbances and their higher competitive ability. This recent and rapid transition from conifers to broadleaves has important implications in forest dynamics and ecosystem services they provide. The finding raises the question as to whether the increasing dominance of relatively drought-sensitive broadleaf species will diminish resilience of Mediterranean forests to very likely drier conditions in the future.

  12. Emerging infectious disease leads to rapid population declines of common British birds.

    Directory of Open Access Journals (Sweden)

    Robert A Robinson

    Full Text Available Emerging infectious diseases are increasingly cited as threats to wildlife, livestock and humans alike. They can threaten geographically isolated or critically endangered wildlife populations; however, relatively few studies have clearly demonstrated the extent to which emerging diseases can impact populations of common wildlife species. Here, we report the impact of an emerging protozoal disease on British populations of greenfinch Carduelis chloris and chaffinch Fringilla coelebs, two of the most common birds in Britain. Morphological and molecular analyses showed this to be due to Trichomonas gallinae. Trichomonosis emerged as a novel fatal disease of finches in Britain in 2005 and rapidly became epidemic within greenfinch, and to a lesser extent chaffinch, populations in 2006. By 2007, breeding populations of greenfinches and chaffinches in the geographic region of highest disease incidence had decreased by 35% and 21% respectively, representing mortality in excess of half a million birds. In contrast, declines were less pronounced or absent in these species in regions where the disease was found in intermediate or low incidence. Also, populations of dunnock Prunella modularis, which similarly feeds in gardens, but in which T. gallinae was rarely recorded, did not decline. This is the first trichomonosis epidemic reported in the scientific literature to negatively impact populations of free-ranging non-columbiform species, and such levels of mortality and decline due to an emerging infectious disease are unprecedented in British wild bird populations. This disease emergence event demonstrates the potential for a protozoan parasite to jump avian host taxonomic groups with dramatic effect over a short time period.

  13. Probing gluon saturation with next-to-leading order photon production at central rapidities in proton-nucleus collisions

    CERN Document Server

    Benic, Sanjin; Garcia-Montero, Oscar; Venugopalan, Raju

    2016-01-01

    We compute the cross section for photons emitted from sea quarks in proton-nucleus collisions at collider energies. The computation is performed within the dilute-dense kinematics of the Color Glass Condensate (CGC) effective field theory. Albeit the result obtained is formally at next-to-leading order in the CGC power counting, it provides the dominant contribution for central rapidities. We observe that the inclusive photon cross section is proportional to all-twist Wilson line correlators in the nucleus. These correlators also appear in quark-pair production; unlike the latter, photon production is insensitive to hadronization uncertainties and therefore more sensitive to multi-parton correlations in the gluon saturation regime of QCD. We demonstrate that $k_\\perp$ and collinear factorized expressions for inclusive photon production are obtained as leading twist approximations to our result. In particular, the collinearly factorized expression is directly sensitive to the nuclear gluon distribution at smal...

  14. Evidence for Patterns of Selective Urban Migration in the Greater Indus Valley (2600-1900 BC: A Lead and Strontium Isotope Mortuary Analysis.

    Directory of Open Access Journals (Sweden)

    Benjamin Valentine

    Full Text Available Just as modern nation-states struggle to manage the cultural and economic impacts of migration, ancient civilizations dealt with similar external pressures and set policies to regulate people's movements. In one of the earliest urban societies, the Indus Civilization, mechanisms linking city populations to hinterland groups remain enigmatic in the absence of written documents. However, isotopic data from human tooth enamel associated with Harappa Phase (2600-1900 BC cemetery burials at Harappa (Pakistan and Farmana (India provide individual biogeochemical life histories of migration. Strontium and lead isotope ratios allow us to reinterpret the Indus tradition of cemetery inhumation as part of a specific and highly regulated institution of migration. Intra-individual isotopic shifts are consistent with immigration from resource-rich hinterlands during childhood. Furthermore, mortuary populations formed over hundreds of years and composed almost entirely of first-generation immigrants suggest that inhumation was the final step in a process linking certain urban Indus communities to diverse hinterland groups. Additional multi disciplinary analyses are warranted to confirm inferred patterns of Indus mobility, but the available isotopic data suggest that efforts to classify and regulate human movement in the ancient Indus region likely helped structure socioeconomic integration across an ethnically diverse landscape.

  15. Precambrian crustal evolution and Cretaceous–Palaeogene faulting in West Greenland: A lead isotope study of an Archaean gold prospect in the Attu region, Nagssugtoqidian orogen, West Greenland

    Directory of Open Access Journals (Sweden)

    Stendal, Henrik

    2006-12-01

    Full Text Available This paper presents a lead isotope investigation of a gold prospect south of the village Attu in the northern part of the Nagssugtoqidian orogen in central West Greenland. The Attu gold prospect is a replacement gold occurrence, related to a shear/mylonite zone along a contact between orthogneissand amphibolite within the Nagssugtoqidian orogenic belt. The mineral occurrence is small, less than 0.5 m wide, and can be followed along strike for several hundred metres. The mineral assemblage is pyrite, chalcopyrite, magnetite and gold. The host rocks to the gold prospect are granulite facies ‘brown gneisses’ and amphibolites. Pb-isotopic data on magnetite from the host rocks yield an isochron in a 207Pb/204Pb vs. 206Pb/204Pb diagram, giving a date of 3162 ± 43 Ma (MSWD = 0.5. This date is interpreted to represent the age of the rocks in question, and is older than dates obtained from rocks elsewhere within the Nagssugtoqidian orogen. Pb-isotopic data on cataclastic magnetite from the shear zone lie close to this isochron, indicating a similar origin. The Pb-isotopic compositions of the ore minerals are similar to those previously obtained from the close-by ~2650 Ma Rifkol granite, and suggest a genetic link between the emplacement of this granite and the formation of the ore minerals in the shear/mylonite zone. Consequently, the age of the gold mineralisation is interpreted tobe late Archaean.

  16. Evidence for Patterns of Selective Urban Migration in the Greater Indus Valley (2600-1900 BC): A Lead and Strontium Isotope Mortuary Analysis

    Science.gov (United States)

    Valentine, Benjamin; Kamenov, George D.; Kenoyer, Jonathan Mark; Shinde, Vasant; Mushrif-Tripathy, Veena; Otarola-Castillo, Erik; Krigbaum, John

    2015-01-01

    Just as modern nation-states struggle to manage the cultural and economic impacts of migration, ancient civilizations dealt with similar external pressures and set policies to regulate people’s movements. In one of the earliest urban societies, the Indus Civilization, mechanisms linking city populations to hinterland groups remain enigmatic in the absence of written documents. However, isotopic data from human tooth enamel associated with Harappa Phase (2600-1900 BC) cemetery burials at Harappa (Pakistan) and Farmana (India) provide individual biogeochemical life histories of migration. Strontium and lead isotope ratios allow us to reinterpret the Indus tradition of cemetery inhumation as part of a specific and highly regulated institution of migration. Intra-individual isotopic shifts are consistent with immigration from resource-rich hinterlands during childhood. Furthermore, mortuary populations formed over hundreds of years and composed almost entirely of first-generation immigrants suggest that inhumation was the final step in a process linking certain urban Indus communities to diverse hinterland groups. Additional multi disciplinary analyses are warranted to confirm inferred patterns of Indus mobility, but the available isotopic data suggest that efforts to classify and regulate human movement in the ancient Indus region likely helped structure socioeconomic integration across an ethnically diverse landscape. PMID:25923705

  17. 南京栖霞山铅锌矿区铅同位素示踪%Lead Isotopes as Tracers in the Qixiashang Lead-Zinc Mining Area,Nanjing

    Institute of Scientific and Technical Information of China (English)

    储彬彬; 罗立强; 王晓芳; 刘颖; 伯英

    2012-01-01

    南京栖霞山铅锌矿已开采50余年,环境问题日益突出.为了了解污染来源和污染传播方式,采集了该地水、土、植物、大气沉降、燃油灰尘、矿石、人血和生物等多种样品进行重金属元素含量和铅同位素示踪分析.结果表明矿区重金属污染严重,且污染随着靠近矿区而逐渐加重,重金属元素Pb、As、Cd、Cu、Zn之间相关性明显,初步反映了污染与矿山有关;同位素分析显示,矿区大气沉降样品、大部分植物样品、部分土壤和部分生物样品铅同位素组成与矿石铅同位素组成相似,证实了污染源为矿山.另外,大气沉降与植物样品铅含量高且它们的铅同位素组成相当,反映了大气沉降是污染传播方式之一.%The Qixiashan lead-zinc mine in Nanjing has been exploited for more than 50 years, and environmental pollution has become increasingly serious. In order to investigate the source and dispersion of the pollution, the authors collected water, soil, plants, atmospheric deposition, vehicle exhaust dust, ore, human blood and biological samples and analyzed heavy metals concentrations and lead isotopes with ICP-MS. The results show that the concentrations of heavy metals in soil, plants, and atmospheric deposition are very high, and the nearer to the mining area, the heavier the pollution. In addition, Pb, As, Cd, Cu and Zn show obvious correlation. Analyses of lead isotopes show that the lead isotope compositions in atmospheric deposition, plants, and part of soils and biological samples around the mining area are similar to those in ores, indicating that the pollution source has been derived form the mine. Furthermore, atmospheric deposition and plants have high lead concentrations and similar lead isotope compositions, suggesting that lead in atmospheric deposition contributes substantially to lead transfer.

  18. Archaeological reconstruction of medieval lead production: Implications for ancient metal provenance studies and paleopollution tracing by Pb isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Baron, Sandrine, E-mail: baron@lmtg.obs-mip.fr [Laboratoire des Travaux et Recherches Archeologiques sur les Cultures, les Espaces et les Societes, Universite Toulouse 2 Le Mirail, CNRS UMR 5608, Maison de la Recherche, 5 allee Antonio-Machado, 31 058 Toulouse Cedex 09 (France); Centre de Recherches Petrographiques et Geochimiques, Nancy Universite, CNRS UPR 2300, BP 20, 15 rue Notre Dame des Pauvres, 54 501 Vandoeuvre-les-Nancy (France); Le-Carlier, Cecile [Centre de Recherche en Archeologie, Archeosciences, Histoire, Universite Rennes 1, CNRS UMR 6566, Bat 24-25, Campus de Beaulieu 35042 Rennes, Cedex (France); Carignan, Jean; Ploquin, Alain [Centre de Recherches Petrographiques et Geochimiques, Nancy Universite, CNRS UPR 2300, BP 20, 15 rue Notre Dame des Pauvres, 54 501 Vandoeuvre-les-Nancy (France)

    2009-11-15

    The identification of metal provenance is often based on chemical and Pb isotope analyses of materials from the operating chain, mainly ores and metallic artefacts. Such analyses, however, have their limits. Some studies are unable to trace metallic artefacts or ingots to their ore sources, even in well-constrained archaeological contexts. Possible reasons for this difficulty are to be found among a variety of limiting factors: (i) problems of ore signatures, (ii) mixing of different ores (alloys), (iii) the use of additives during the metallurgical process, (iv) metal recycling and (v) possible Pb isotopic fractionation during metal production. This paper focuses on the issue of Pb isotope fractionation during smelting to address the issue of metal provenance. Through an experimental reconstruction of argentiferous Pb production in the medieval period, an attempt was made to better understand and interpret the Pb isotopic composition of ore smelting products. It is shown that the measured differences (outside the total external uncertainties of 0.005 (2*sd) for {sup 206}Pb/{sup 204}Pb ratios) in Pb signatures measured between ores, slag and smoke are not due to Pb mass fractionation processes, but to (1) ore heterogeneity ({Delta}{sup 206}Pb/{sup 204}Pb{sub slag-ores} = 0.066) and (2) the use of additives during the metallurgical process ({Delta}{sup 206}Pb/{sup 204}Pb{sub slag-ores} = 0.083). Even if these differences are due to causes (1) and/or (2), smoke from the ore reduction appears to reflect the ore mining area without a significant disturbance of its Pb signature for all the isotopic ratios ({Delta}{sup 206}Pb/{sup 204}Pb{sub smokes-ores} = 0.026). Thus, because the isotopic heterogeneity of the mining district and additives is averaged in slags, slag appears as the most relevant product to identify ancient metal provenance. Whereas aiming at identifying a given mine seems beyond the possibilities provided by the method, searching for the mining district

  19. Lead Isotopes in Olivine-Phyric Shergottite Tissint: Implications for the Geochemical Evolution of the Shergottite Source Mantle

    Science.gov (United States)

    Moriwaki, R.; Usui, T.; Simon, J. I.; Jones, J. H.; Yokoyama, T.

    2015-01-01

    Geochemically-depleted shergottites are basaltic rocks derived from a martian mantle source reservoir. Geochemical evolution of the martian mantle has been investigated mainly based on the Rb-Sr, Sm-Nd, and Lu-Hf isotope systematics of the shergottites [1]. Although potentially informative, U-Th- Pb isotope systematics have been limited because of difficulties in interpreting the analyses of depleted meteorite samples that are more susceptible to the effects of near-surface processes and terrestrial contamination. This study conducts a 5-step sequential acid leaching experiment of the first witnessed fall of the geochemically-depleted olivinephyric shergottite Tissint to minimize the effect of low temperature distrubence. Trace element analyses of the Tissint acid residue (mostly pyroxene) indicate that Pb isotope compositions of the residue do not contain either a martian surface or terrestrial component, but represent the Tissint magma source [2]. The residue has relatively unradiogenic initial Pb isotopic compositions (e.g., 206Pb/204Pb = 10.8136) that fall within the Pb isotope space of other geochemically-depleted shergottites. An initial µ-value (238U/204Pb = 1.5) of Tissint at the time of crystallization (472 Ma [3]) is similar to a time-integrated mu- value (1.72 at 472 Ma) of the Tissint source mantle calculated based on the two-stage mantle evolution model [1]. On the other hand, the other geochemically-depleted shergottites (e.g., QUE 94201 [4]) have initial µ-values of their parental magmas distinctly lower than those of their modeled source mantle. These results suggest that only Tissint potentially reflects the geochemical signature of the shergottite mantle source that originated from cumulates of the martian magma ocean

  20. A rapid spectrophotometric method for the determination of trace level lead using 1,5-diphenylthiocarbazone in aqueous micellar solutions.

    Science.gov (United States)

    Khan, Humaira; Ahmed, M Jamaluddin; Bhanger, M Iqbal

    2007-02-01

    A very simple, ultra-sensitive and fairly selective direct spectrophotmetric method is presented for the rapid determination of lead(II) at ultra-trace level using 1,5-diphenylthiocarbazone (dithizone) in micellar media. The presence of the micellar system avoids the previous steps of solvent extraction and reduces the cost and toxicity while enhancing the sensitivity, selectivity and the molar absorptivity. The molar absorptivities of the lead-dithizone complex formed in the presence of the cationic cetyltrimethylammonium bromide (CTAB) surfactants are almost ten times the value observed in the standard method, resulting in an increase in the sensitivity of the method. The reaction is instantaneous and the absorbance remains stable for over 24 h. The average molar absorption coefficient was found to be 3.99 x 10(5) L mol(-1) cm(-1) and Sandell's sensitivity was 30 ng cm(-2) of Pb. Linear calibration graphs were obtained for 0.06-60 mg L(-1) of Pb(II); the stoichiometric composition of the chelate is 1:2 (Pb:dithizone). The interference from over 50 cations, anions and complexing agents has been studied at 1 mg L(-1) of Pb(II). The method was successfully used in the determination of lead in several standard reference materials (alloys and steels), environmental water samples (potable and polluted), biological samples (human blood and urine), soil samples and solutions containing both lead(II) and lead(IV) and complex synthetic mixtures. The method has high precision and accuracy (sigma = +/-0.01 for 0.5 mg L(-1)).

  1. Monitoring Lead (Pb) Pollution and Identifying Pb Pollution Sources in Japan Using Stable Pb Isotope Analysis with Kidneys of Wild Rats

    Science.gov (United States)

    Nakata, Hokuto; Nakayama, Shouta M. M.; Oroszlany, Balazs; Ikenaka, Yoshinori; Mizukawa, Hazuki; Tanaka, Kazuyuki; Harunari, Tsunehito; Tanikawa, Tsutomu; Darwish, Wageh Sobhy; Yohannes, Yared B.; Saengtienchai, Aksorn; Ishizuka, Mayumi

    2017-01-01

    Although Japan has been considered to have little lead (Pb) pollution in modern times, the actual pollution situation is unclear. The present study aims to investigate the extent of Pb pollution and to identify the pollution sources in Japan using stable Pb isotope analysis with kidneys of wild rats. Wild brown (Rattus norvegicus, n = 43) and black (R. rattus, n = 98) rats were trapped from various sites in Japan. Mean Pb concentrations in the kidneys of rats from Okinawa (15.58 mg/kg, dry weight), Aichi (10.83), Niigata (10.62), Fukuoka (8.09), Ibaraki (5.06), Kyoto (4.58), Osaka (4.57), Kanagawa (3.42), and Tokyo (3.40) were above the threshold (2.50) for histological kidney changes. Similarly, compared with the previous report, it was regarded that even structural and functional kidney damage as well as neurotoxicity have spread among rats in Japan. Additionally, the possibility of human exposure to a high level of Pb was assumed. In regard to stable Pb isotope analysis, distinctive values of stable Pb isotope ratios (Pb-IRs) were detected in some kidney samples with Pb levels above 5.0 mg/kg. This result indicated that composite factors are involved in Pb pollution. However, the identification of a concrete pollution source has not been accomplished due to limited differences among previously reported values of Pb isotope composition in circulating Pb products. Namely, the current study established the limit of Pb isotope analysis for source identification. Further detailed research about monitoring Pb pollution in Japan and the demonstration of a novel method to identify Pb sources are needed. PMID:28075384

  2. Monitoring Lead (Pb Pollution and Identifying Pb Pollution Sources in Japan Using Stable Pb Isotope Analysis with Kidneys of Wild Rats

    Directory of Open Access Journals (Sweden)

    Hokuto Nakata

    2017-01-01

    Full Text Available Although Japan has been considered to have little lead (Pb pollution in modern times, the actual pollution situation is unclear. The present study aims to investigate the extent of Pb pollution and to identify the pollution sources in Japan using stable Pb isotope analysis with kidneys of wild rats. Wild brown (Rattus norvegicus, n = 43 and black (R. rattus, n = 98 rats were trapped from various sites in Japan. Mean Pb concentrations in the kidneys of rats from Okinawa (15.58 mg/kg, dry weight, Aichi (10.83, Niigata (10.62, Fukuoka (8.09, Ibaraki (5.06, Kyoto (4.58, Osaka (4.57, Kanagawa (3.42, and Tokyo (3.40 were above the threshold (2.50 for histological kidney changes. Similarly, compared with the previous report, it was regarded that even structural and functional kidney damage as well as neurotoxicity have spread among rats in Japan. Additionally, the possibility of human exposure to a high level of Pb was assumed. In regard to stable Pb isotope analysis, distinctive values of stable Pb isotope ratios (Pb-IRs were detected in some kidney samples with Pb levels above 5.0 mg/kg. This result indicated that composite factors are involved in Pb pollution. However, the identification of a concrete pollution source has not been accomplished due to limited differences among previously reported values of Pb isotope composition in circulating Pb products. Namely, the current study established the limit of Pb isotope analysis for source identification. Further detailed research about monitoring Pb pollution in Japan and the demonstration of a novel method to identify Pb sources are needed.

  3. Monitoring Lead (Pb) Pollution and Identifying Pb Pollution Sources in Japan Using Stable Pb Isotope Analysis with Kidneys of Wild Rats.

    Science.gov (United States)

    Nakata, Hokuto; Nakayama, Shouta M M; Oroszlany, Balazs; Ikenaka, Yoshinori; Mizukawa, Hazuki; Tanaka, Kazuyuki; Harunari, Tsunehito; Tanikawa, Tsutomu; Darwish, Wageh Sobhy; Yohannes, Yared B; Saengtienchai, Aksorn; Ishizuka, Mayumi

    2017-01-10

    Although Japan has been considered to have little lead (Pb) pollution in modern times, the actual pollution situation is unclear. The present study aims to investigate the extent of Pb pollution and to identify the pollution sources in Japan using stable Pb isotope analysis with kidneys of wild rats. Wild brown (Rattus norvegicus, n = 43) and black (R. rattus, n = 98) rats were trapped from various sites in Japan. Mean Pb concentrations in the kidneys of rats from Okinawa (15.58 mg/kg, dry weight), Aichi (10.83), Niigata (10.62), Fukuoka (8.09), Ibaraki (5.06), Kyoto (4.58), Osaka (4.57), Kanagawa (3.42), and Tokyo (3.40) were above the threshold (2.50) for histological kidney changes. Similarly, compared with the previous report, it was regarded that even structural and functional kidney damage as well as neurotoxicity have spread among rats in Japan. Additionally, the possibility of human exposure to a high level of Pb was assumed. In regard to stable Pb isotope analysis, distinctive values of stable Pb isotope ratios (Pb-IRs) were detected in some kidney samples with Pb levels above 5.0 mg/kg. This result indicated that composite factors are involved in Pb pollution. However, the identification of a concrete pollution source has not been accomplished due to limited differences among previously reported values of Pb isotope composition in circulating Pb products. Namely, the current study established the limit of Pb isotope analysis for source identification. Further detailed research about monitoring Pb pollution in Japan and the demonstration of a novel method to identify Pb sources are needed.

  4. Technical Note: An improved guideline for rapid and precise sample preparation of tree-ring stable isotope analysis

    Science.gov (United States)

    Schollaen, K.; Baschek, H.; Heinrich, I.; Helle, G.

    2015-07-01

    The procedure of wood sample preparation, including tree-ring dissection, cellulose extraction, homogenization and finally weighing and packing for stable isotope analysis is labour intensive and time consuming. We present an elaborated methodical guideline from pre-analyses considerations, wood sample preparation through semi-automated chemical extraction of cellulose directly from tree-ring cross-sections to tree-ring dissection for high-precision isotope ratio mass spectrometry. This guideline reduces time and maximizes the tree-ring stable isotope data throughput significantly. The method was applied to ten different tree species (coniferous and angiosperm wood) with different wood growth rates and differently shaped tree-ring boundaries. The tree-ring structures of the cellulose cross-sections largely remained well identifiable. FTIR (Fourier transform infrared) spectrometry and the comparison of stable isotope values with classical method confirm chemical purity of the resultant cellulose. Sample homogenization is no longer necessary. Cellulose extraction is now faster, cheaper and more user friendly allowing (i) the simultaneous treatment of wood cross-sections of a total length of 180 cm (equivalent to 6 increment cores of 30 cm length) and thickness of 0.5 to 2 mm, and (ii) precise tree-ring separation at annual to high-resolution scale utilizing manual devices or UV-laser microdissection microscopes.

  5. Technical Note: An improved guideline for rapid and precise sample preparation of tree-ring stable isotope analysis

    Directory of Open Access Journals (Sweden)

    K. Schollaen

    2015-07-01

    Full Text Available The procedure of wood sample preparation, including tree-ring dissection, cellulose extraction, homogenization and finally weighing and packing for stable isotope analysis is labour intensive and time consuming. We present an elaborated methodical guideline from pre-analyses considerations, wood sample preparation through semi-automated chemical extraction of cellulose directly from tree-ring cross-sections to tree-ring dissection for high-precision isotope ratio mass spectrometry. This guideline reduces time and maximizes the tree-ring stable isotope data throughput significantly. The method was applied to ten different tree species (coniferous and angiosperm wood with different wood growth rates and differently shaped tree-ring boundaries. The tree-ring structures of the cellulose cross-sections largely remained well identifiable. FTIR (Fourier transform infrared spectrometry and the comparison of stable isotope values with classical method confirm chemical purity of the resultant cellulose. Sample homogenization is no longer necessary. Cellulose extraction is now faster, cheaper and more user friendly allowing (i the simultaneous treatment of wood cross-sections of a total length of 180 cm (equivalent to 6 increment cores of 30 cm length and thickness of 0.5 to 2 mm, and (ii precise tree-ring separation at annual to high-resolution scale utilizing manual devices or UV-laser microdissection microscopes.

  6. Determination of the geographic origin of rice by chemometrics with strontium and lead isotope ratios and multielement concentrations.

    Science.gov (United States)

    Ariyama, Kaoru; Shinozaki, Miyuki; Kawasaki, Akira

    2012-02-22

    The objective of this study was to develop a technique for determining the country of origin of rice in the Japanese market. The rice samples included a total of 350 products grown in Japan (n = 200), the United States (n = 50), China (n = 50), and Thailand (n = 50). In this study, (87)Sr/(86)Sr and Pb isotope ((204)Pb, (206)Pb, (207)Pb, and (208)Pb) ratios and multielement concentrations (Al, Fe, Co, Ni, Cu, Rb, Sr, and Ba) were determined by high-resolution inductively coupled plasma mass spectrometry. By combining three chemometric techniques based on different principles and determination criteria, the countries of origin of rice were determined. The predictions made by 10-fold cross-validation were around 97% accurate. The presented method demonstrated the effectiveness of determining the geographic origin of an agricultural product by combining several chemometric techniques using heavy element isotope ratios and multielement concentrations.

  7. Aerobic respiration along isopycnals leads to overestimation of the isotope effect of denitrification in the ocean water column

    Science.gov (United States)

    Marconi, Dario; Kopf, Sebastian; Rafter, Patrick A.; Sigman, Daniel M.

    2017-01-01

    The nitrogen (N) isotopes provide an integrative geochemical tool for constraining the fixed N budget of the ocean. However, N isotope budgeting requires a robust estimate for the organism-scale nitrogen isotope effect of denitrification, in particular as it occurs in water column denitrification zones (εwcd). Ocean field data interpreted with the Rayleigh model have typically yielded estimates for εwcd of between 20 and 30‰. However, recent findings have raised questions about this value. In particular, culture experiments can produce a substantially lower isotope effect (∼13‰) under conditions mimicking those of ocean suboxic zones. In an effort to better understand prior field estimates of εwcd, we use a geochemical multi-box model to investigate the combined effects of denitrification, aerobic respiration, and isopycnal exchange on the δ15N of nitrate. In the context of this admittedly simplistic model, we consider three isopycnals extending from the Southern Ocean to the Eastern Tropical North Pacific (ETNP). We show that the data from the ETNP suboxic zone can be reproduced with an εwcd of 13‰, given a rate of aerobic respiration consistent with the nutrient data on these isopycnals and a plausible range in the δ15N of the sinking flux being remineralized. We discuss the limitations of our analysis, additional considerations, as well as possible data-based tests for the proposal of a lower εwcd than previously estimated. All else held constant, a lower εwcd would imply a lower global ocean rate of denitrification that is more similar to the estimated rate of N input to the global ocean, providing a major impetus for further investigation.

  8. Lead Isotope Compositions of Acid Residues from Olivine-Phyric Shergottite Tissint: Implications for Heterogeneous Shergottite Source Reservoirs

    Science.gov (United States)

    Moriwaki, R.; Usui, T.; Yokoyama, T.; Simon, J. I.; Jones, J. H.

    2015-01-01

    Geochemical studies of shergottites suggest that their parental magmas reflect mixtures between at least two distinct geochemical source reservoirs, producing correlations between radiogenic isotope compositions and trace element abundances. These correlations have been interpreted as indicating the presence of a reduced, incompatible element- depleted reservoir and an oxidized, incompatible- element-enriched reservoir. The former is clearly a depleted mantle source, but there is ongoing debate regarding the origin of the enriched reservoir. Two contrasting models have been proposed regarding the location and mixing process of the two geochemical source reservoirs: (1) assimilation of oxidized crust by mantle derived, reduced magmas, or (2) mixing of two distinct mantle reservoirs during melting. The former requires the ancient Martian crust to be the enriched source (crustal assimilation), whereas the latter requires isolation of a long-lived enriched mantle domain that probably originated from residual melts formed during solidification of a magma ocean (heterogeneous mantle model). This study conducts Pb isotope and trace element concentration analyses of sequential acid-leaching fractions (leachates and the final residues) from the geochemically depleted olivine-phyric shergottite Tissint. The results suggest that the Tissint magma is not isotopically uniform and sampled at least two geochemical source reservoirs, implying that either crustal assimilation or magma mixing would have played a role in the Tissint petrogenesis.

  9. Anthropogenic influences on Pb/Al and lead isotope signature in annually layered Holocene Maar lake sediments

    Energy Technology Data Exchange (ETDEWEB)

    Schettler, G.; Romer, R.L. [GeoForschungsZentrum Potsdam, Telegrafenberg, D-14473 Potsdam (Germany)

    1998-08-01

    Annually laminated sediments from two Maar lakes in the West Eifel volcanic field (Germany) show anomalously high Pb within sections deposited during the first centuries A.D. exceeding the local geological background 8.5-fold in Lake Meerfelder Maar (MFM) and 4-fold in Lake Schalkenmehrener Maar (SMM). These Pb anomalies are associated with a distinct shift in the Pb isotope signature to less radiogenic compositions. The excess Pb causing the anomaly has the same isotopic composition as galena deposits 60 km to the NW of the Maar lakes. It is suggested that this component was transported airborne into the Maar lakes and originates from regional Roman Pb refinement and cupellation of argentiferous Pb. Varve chronostratigraphy of correlated cores indicates that significant Roman Pb input lasted for about 230 a. SMM does not get fluviatile input. Its sedimentary record is more sensitive to variations in airborne input than that of MFM, which had an inflow. SMM sediment sections deposited during periods of low soil erosion (early Holocene, Dark Ages) with comparably high Pb/Al values also show little radiogenic Pb. This is caused by airborne minerogenic matter from a geochemically and isotopically distinct remote source that becomes apparent only in sedimentation periods of very restricted local allochthonous input. (Copyright (c) 1998 Elsevier Science B.V., Amsterdam. All rights reserved.)

  10. Lead isotopes and heavy minerals analyzed as tools to understand the distribution of lead and other potentially toxic elements in soils contaminated by Cu smelting (Legnica, Poland).

    Science.gov (United States)

    Tyszka, Rafał; Pietranik, Anna; Kierczak, Jakub; Ettler, Vojtěch; Mihaljevič, Martin; Medyńska-Juraszek, Agnieszka

    2016-12-01

    Surroundings of the Legnica Cu smelter (Poland) offer insight into the behavior of Pb and other metal(oid)s in heavily contaminated soils in a relatively simple site, where lithogenic and anthropogenic Pb contributions have uniform Pb isotope composition over the time of smelter activity. Distribution of metal(oid)s decreases asymptotically with depth and below 30 cm reaches concentrations typical or lower than those of upper continental crust. Usually, such distribution is interpreted as the decrease in anthropogenic Pb contribution with depth. However, calculations based on Pb isotopes indicate that anthropogenic Pb is probably distributed both as Pb-rich particles of slags and fly ashes and Pb-poor soil solutions. Generally, anthropogenic Pb constitutes up to 100 % of Pb in the uppermost 10 cm of the soils and comes often from mechanical mixing with slag and fly ash particles as well as their weathering products. On the other hand, lower soil horizon contains anthropogenic Pb in various forms, and at depths below 30 cm, most of anthropogenic Pb comes from soil solutions and can constitute from 1 to 65 % of the Pb budget. This is consistent with secondary electron microscope (SEM) analyses of heavy mineral particles showing that, in upper horizons, Pb, Cu, and Zn are contained in various particles emitted from the smelter, which show different stages of weathering. Currently, large portion of these metals may reside in the secondary Fe-hydro-oxides. On the other hand, in deeper soil horizons, anthropogenic Pb is probably dominated by Pb coming from leaching of slag or fly ash particles. Overall, metal(oid) mobility is a dynamic process and is controlled by the soil type (cultivated versus forest) and the composition and the structure of the metal-rich particles emitted from the smelter. High proportions of anthropogenic Pb at depths below 30 cm in some soil profiles indicate that Pb (and probably other metal(oid)s) can be transported down the soil profile

  11. Determination of trace element concentrations and stable lead, uranium and thorium isotope ratios by quadrupole-ICP-MS in NORM and NORM-polluted sample leachates.

    Science.gov (United States)

    Mas, J L; Villa, M; Hurtado, S; García-Tenorio, R

    2012-02-29

    This work focuses on the monitoring of the potential pollution in scenarios that involve NORM-related industrial activities (environmental or in-door scenarios). The objective was to develop a method to determine extent and origin of the contamination, suitable for monitoring (i.e. simple, fast and economical) and avoiding the use of too many different instruments. It is presented a radiochemical method that allows the determination of trace element concentrations and 206Pb/207Pb/208Pb, 238U/234U and 232Th/230Th isotope ratios using a single sample aliquot and a single instrument (ICP-QMS). Eichrom UTEVA® extraction chromatography minicolumns were used to separate uranium and thorium in sample leachates. Independent ICP-MS determinations of uranium and thorium isotope ratios were carried out afterwards. Previously a small aliquot of the leachate was used for the determination of trace element concentrations and lead isotope ratios. Several radiochemical arrangements were tested to get maximum performances and simplicity of the method. The performances of the method were studied in terms of chemical yields of uranium and thorium and removal of the potentially interfering elements. The established method was applied to samples from a chemical industry and sediments collected in a NORM-polluted scenario. The results obtained from our method allowed us to infer not only the extent, but also the sources of the contamination in the area. Copyright © 2012 Elsevier B.V. All rights reserved.

  12. A study of radionuclides, metals and stable lead isotope ratios in sediments and soils in the vicinity of natural U-mineralisation areas in the Northern Territory

    Energy Technology Data Exchange (ETDEWEB)

    Frostick, A., E-mail: Alison.Frostick@cdu.edu.au [Charles Darwin University, School of Environment and Life Sciences, Darwin NT 0909 (Australia); ERISS, GPO Box 461, Darwin NT 0801 (Australia); Bollhoefer, A. [ERISS, GPO Box 461, Darwin NT 0801 (Australia); Parry, D. [AIMS, PO Box 41775, Casuarina NT 0811 (Australia)

    2011-10-15

    Australian guidelines recommend that tailings materials from uranium (U) mining and milling be contained without any detrimental impact on the environment for at least 1000 years. Natural analogue sites are being investigated to determine if they can provide data on the rates of natural erosion processes which occur over these timescales, for input into predictive geomorphic computer models. This paper presents radionuclide, metal and stable lead (Pb) isotope data from sediment cores and surface soils in the vicinity of two mineralised areas in the Alligator Rivers Region. Surface scrapes from the natural Anomaly no. 2, south of the Ranger mineral lease, exhibit radiogenic {sup 206}Pb/{sup 207}Pb and {sup 208}Pb/{sup 207}Pb ratios, and elevated U and metal concentrations typical for a near surface U anomaly. In contrast, samples taken from the Koongarra mineral lease (KML) show radionuclide activity and metal concentrations similar to natural areas elsewhere in the Alligator Rivers Region and Pb isotope ratios are closer to present day average crustal ratios (PDAC), as the orebodies at KML are covered by surficial sand. A sediment core collected from Anbangbang Billabong, downstream of KML, exhibits small variations in Pb isotope ratios that indicate that approximately 1% of the upper sediments in the sediment core may be derived from material originating from the U anomaly at Koongarra.

  13. The electrooxidation mechanism of formic acid on platinum and on lead ad-atoms modified platinum studied with the kinetic isotope effect

    Science.gov (United States)

    Bełtowska-Brzezinska, M.; Łuczak, T.; Stelmach, J.; Holze, R.

    2014-04-01

    Kinetics and mechanism of formic acid (FA) oxidation on platinum and upd-lead ad-atoms modified platinum electrodes have been studied using unlabelled and deuterated compounds. Poisoning of the electrode surface by CO-like species was prevented by suppression of dissociative chemisorption of FA due to a fast competitive underpotential deposition of lead ad-atoms on the Pt surface from an acidic solution containing Pb2+ cations. Modification of the Pt electrode with upd lead induced a catalytic effect in the direct electrooxidation of physisorbed FA to CO2. With increasing degree of H/D substitution, the rate of this reaction decreased in the order: HCOOH > DCOOH ≥ HCOOD > DCOOD. HCOOH was oxidized 8.5-times faster on a Pt/Pb electrode than DCOOD. This primary kinetic isotope effect proves that the C-H- and O-H-bonds are simultaneously cleaved in the rate determining step. A secondary kinetic isotope effect was found in the dissociative chemisorption of FA in the hydrogen adsorption-desorption range on a bare Pt electrode after H/D exchange in the C-H bond, wherein the influence of deuterium substitution in the O-H group was negligibly small. Thus the C-H bond cleavage is accompanied by the C-OH and not the O-H bond split in the FA decomposition, producing CO-like species on the Pt surface sites.

  14. Determination of the provenance of cocoa by soil protolith ages and assessment of anthropogenic lead contamination by pb/nd and lead isotope ratios.

    Science.gov (United States)

    Manton, William I

    2010-01-27

    The Pb contents of chocolate and the products it flavors are among the highest of all commonly consumed substances. Others have shown that this Pb is acquired by cocoa beans after harvesting and is concentrated in their shells, portions of which are ground up with the cotyledons during processing. It is shown here that the shells also contain the lanthanides Nd and Sm, which they appear to take up more slowly than Pb when dried on bare soil. Consideration of Pb/Nd ratios, model Sm-Nd ages and the isotope ratios of Pb and Sr indicates that, in the absence of contamination, the relationship between Pb and Nd in shells is y = 13.1x(-0.383), where x is the Nd concentration in microg/kg and y is the Pb/Nd ratio. For cocoa powders, the relationship is y = 114x(-0.988). Samples that plot above these curves are probably contaminated. Model ages indicate where the cocoa of cocoa powders is grown, and these same considerations point to African samples being uncontaminated but samples from Asia containing 50% anthropogenic Pb of Australian origin. No measurable Pb contamination occurs during the transport of beans and the manufacture of chocolate.

  15. Helium, lead and sulfur isotope geochemistry of the Gejiu Sn-polymetallic ore deposit and the sources of ore-forming materials

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Studies on the helium, lead and sulfur isotopic composition were performed of the Gejiu super-large Sn-polymetallic ore deposit. The results indicated that the ore-forming materials came from different sources and the deposit is a product of superimposed mineralization. The deposit is characterized by multi-source and multi-period mineralization, which experienced submarine hydrothermal deposition and Late Yanshanian magmatic hydrothermal mineralization. It is held that the Gejiu super-large Sn-polymetallic ore deposit is a multi-genesis deposit.

  16. Rapid biosynthesis of stable isotope-labeled peptides from a reconstituted in vitro translation system for targeted proteomics.

    Science.gov (United States)

    Xian, Feng; Li, Shuwei; Liu, Siqi

    2015-01-01

    Stable isotope-labeled peptides are routinely used as internal standards (a.k.a. reference peptides) for absolute quantitation of proteins in targeted proteomics. These peptides can either be synthesized chemically on solid supports or expressed biologically by concatenating multiple peptides together to a large protein. Neither method, however, has required versatility, convenience, and economy for making a large number of reference peptides. Here, we describe the biosynthesis of stable isotope-labeled peptides from a reconstituted Escherichia coli in vitro translation system. We provide a detailed protocol on how to express these peptides with high purity and how to determine their concentrations with easiness. Our strategy offers a general, fast, and scalable approach for the easy preparation of labeled reference peptides, which will have broad application in both basic research and translational medicine.

  17. Determination of trace element concentrations and stable lead, uranium and thorium isotope ratios by quadrupole-ICP-MS in NORM and NORM-polluted sample leachates

    Energy Technology Data Exchange (ETDEWEB)

    Mas, J.L., E-mail: ppmasb@us.es [Dpto. Fisica Aplicada I, EPS, Universidad de Sevilla, 41012 Sevilla (Spain); Villa, M. [Servicio de Radioisotopos, Centro de Investigacion, Tecnologia e Innovacion (CITIUS), Universidad de Sevilla, Avda. Reina Mercedes 4b, 41012 Sevilla (Spain); Dpto. Fisica Aplicada II, ETS de Arquitectura, Universidad de Sevilla, Avda. Reina Mercedes 2, 41012 Sevilla (Spain); Hurtado, S. [Servicio de Radioisotopos, Centro de Investigacion, Tecnologia e Innovacion (CITIUS), Universidad de Sevilla, Avda. Reina Mercedes 4b, 41012 Sevilla (Spain); Garcia-Tenorio, R. [Dpto. Fisica Aplicada II, ETS de Arquitectura, Universidad de Sevilla, Avda. Reina Mercedes 2, 41012 Sevilla (Spain)

    2012-02-29

    Highlights: Black-Right-Pointing-Pointer Polluted sediment and NORM samples. Black-Right-Pointing-Pointer An efficient yet fast process allowing multi-parametric determinations in <3 days. Black-Right-Pointing-Pointer Trace element concentrations, Pb, Th and U isotope ratios with a single instrument. - Abstract: This work focuses on the monitoring of the potential pollution in scenarios that involve NORM-related industrial activities (environmental or in-door scenarios). The objective was to develop a method to determine extent and origin of the contamination, suitable for monitoring (i.e. simple, fast and economical) and avoiding the use of too many different instruments. It is presented a radiochemical method that allows the determination of trace element concentrations and {sup 206}Pb/{sup 207}Pb/{sup 208}Pb, {sup 238}U/{sup 234}U and {sup 232}Th/{sup 230}Th isotope ratios using a single sample aliquot and a single instrument (ICP-QMS). Eichrom UTEVA{sup Registered-Sign} extraction chromatography minicolumns were used to separate uranium and thorium in sample leachates. Independent ICP-MS determinations of uranium and thorium isotope ratios were carried out afterwards. Previously a small aliquot of the leachate was used for the determination of trace element concentrations and lead isotope ratios. Several radiochemical arrangements were tested to get maximum performances and simplicity of the method. The performances of the method were studied in terms of chemical yields of uranium and thorium and removal of the potentially interfering elements. The established method was applied to samples from a chemical industry and sediments collected in a NORM-polluted scenario. The results obtained from our method allowed us to infer not only the extent, but also the sources of the contamination in the area.

  18. Uranium-lead Isotope Evidence in the Shelyabinsk LL5 Chondrite Meteorite for Ancient and Recent Thermal Events

    Science.gov (United States)

    Lapen, T. J.; Kring, D. A.; Zolensky, M. E.; Andreasen, R.; Righter, M.; Swindle, T. D.; Beard, S. P.; Swindle, T. D.

    2014-01-01

    The impact histories on chondrite parent bodies can be deduced from thermochronologic analyses of materials and isotope systems with distinct apparent closure temperatures. It is especially critical to better understand the geological histories and physical properties of potenally hazardous near-Earth asteroids. Chelyabinsk is an LL5 chondrite meteorite that was dispersed over a wide area tens of kilometers south of the town of Chelyabinsk, Russia by an explosion at an altitude of 27 km at 3:22 UT on 15 Feb 2013 [1,2]. The explosion resulted in significant damage to surrounding areas and over 1500 injuries along with meteorite fragments being spread over a wide area [1].

  19. Dike intrusions into bituminous coal, Illinois Basin: H, C, N, O isotopic responses to rapid and brief heating

    Science.gov (United States)

    Schimmelmann, A.; Mastalerz, Maria; Gao, L.; Sauer, P.E.; Topalov, K.

    2009-01-01

    Unlike long-term heating in subsiding sedimentary basins, the near-instantaneous thermal maturation of sedimentary organic matter near magmatic intrusions is comparable to artificial thermal maturation in the laboratory in terms of short duration and limited extent. This study investigates chemical and H, C, N, O isotopic changes in high volatile bituminous coal near two Illinois dike contacts and compares observed patterns and trends with data from other published studies and from artificial maturation experiments. Our study pioneers in quantifying isotopically exchangeable hydrogen and measuring the D/H (i.e., 2H/1H) ratio of isotopically non-exchangeable organic hydrogen in kerogen near magmatic contacts. Thermal stress in coal caused a reduction of isotopically exchangeable hydrogen in kerogen from 5% to 6% in unaltered coal to 2-3% at contacts, mostly due to elimination of functional groups (e.g., {single bond}OH, {single bond}COOH, {single bond}NH2). In contrast to all previously published data on D/H in thermally matured organic matter, the more mature kerogen near the two dike contacts is D-depleted, which is attributed to (i) thermal elimination of D-enriched functional groups, and (ii) thermal drying of hydrologically isolated coal prior to the onset of cracking reactions, thereby precluding D-transfer from relatively D-enriched water into kerogen. Maxima in organic nitrogen concentration and in the atomic N/C ratio of kerogen at a distance of ???2.5 to ???3.5 m from the thicker dike indicate that reactive N-compounds had been pyrolytically liberated at high temperature closer to the contact, migrated through the coal seam, and recombined with coal kerogen in a zone of lower temperature. The same principle extends to organic carbon, because a strong ??13Ckerogen vs. ??15Nkerogen correlation across 5.5 m of coal adjacent to the thicker dike indicates that coal was functioning as a flow-through reactor along a dynamic thermal gradient facilitating back

  20. Identification of trace metal pollution in urban dust from kindergartens using magnetic, geochemical and lead isotopic analyses

    Science.gov (United States)

    Zhu, Zongmin; Sun, Guangyi; Bi, Xiangyang; Li, Zhonggen; Yu, Genhua

    2013-10-01

    In the present study, magnetic measurements were combined with geochemical analysis and stable Pb isotopic ratios to reveal the distribution and origination of trace metal pollutants in kindergarten dusts from a typical urban environment of Wuhan, central China. The geoaccumulation index (Igeo) of magnetic properties was more prominent than those of individual metals. The magnetic susceptibility (MS) and trace metals (Zn, Pb, and Cu) in this study together with published results from other Chinese cities formed a liner relationship, suggesting that metal contaminants in Chinese urban areas had similar MS to metal ratios, which could be used as an indicator for identification of pollution sources between Chinese cities and the other Asian cities. Stable Pb isotopic ratios (1.1125-1.1734 for 206Pb/207Pb and 2.4457-2.4679 for 208Pb/207Pb) in the urban dusts from Wuhan were characterized by higher 208Pb component in comparison with those from other Chinese cities. This result combined with principal component analysis (PCA) indicated that metal pollutants in the dusts were derived from industrial activities and coal combustion, whereas the traffic emissions were no longer a predominant pollution source in urban environment. Our study demonstrated that environmental magnetic methods could not only reveal the overall situation of trace metal contamination, but also prove evidence in the identification of pollution sources.

  1. Uranium-Lead Zircon Ages and Sr, Nd, and Pb Isotope Geochemistry of Selected Plutonic Rocks from Western Idaho

    Science.gov (United States)

    Unruh, Daniel M.; Lund, Karen; Kuntz, Mel A.; Snee, Lawrence W.

    2008-01-01

    Across the Salmon River suture in western Idaho, where allochthonous Permian to Cretaceous oceanic rocks are juxtaposed against Proterozoic North American rocks, a wide variety of plutonic rocks are exposed. Available data indicate much variation in composition, source, and structural state of these plutons. The plutonic rocks were long described as the western border zone of the Cretaceous Idaho batholith but limited pre-existing age data indicate more complicated origins. Because the affinity and age of the plutonic rocks cannot be reliably determined from field relations, TIMS U-Pb dating in conjunction with Sr, Nd, and Pb isotopic studies of selected plutons across the suture in western Idaho were undertaken. The data indicate three general groups of plutons including (1) those that intruded the island arc terranes during the Triassic and Jurassic, those that intruded near the western edge of oceanic rocks along the suture in the Early Cretaceous, and the plutons of the Idaho batholith that intruded Proterozoic North American rocks in the Late Cretaceous. Plutons that intruded Proterozoic North American rocks commonly include xenocrystic zircons and in several cases, ages could not be determined. The least radiogenic Sr and most radiogenic Nd are found among the Blue Mountains superterrane island arc samples. Suture-zone plutons have isotopic characteristics that span the range between Idaho batholith and island arc samples but mostly follow island arc signatures. Plutons of the Idaho batholith have the most radiogenic initial Pb and Sr ratios and the least radiogenic Nd of the samples analyzed.

  2. Uranium-lead dating method at the Pará-Iso isotope geology laboratory, UFPA, Belém - Brazil

    Directory of Open Access Journals (Sweden)

    Robert S. Krymsky

    2007-03-01

    Full Text Available Analytical procedures for U-Pb isotope dilution analyses at the Pará-Iso isotope geology laboratory of the Federal University of Pará (UFPA are described in detail. The procedures are applied to zircon, titanite, rutile, apatite, columbite-tantalite and whole rock. Reagent preparation and chemical processing are done in clean-room conditions. Samples are dissolved using TeflonTM microcapsules in steel jacket TeflonTM Parr InstrumentTM bomb or TeflonTM screw cap containers. U and Pb are separated using anion exchange AG 1x8 resin columns. Typical blanks for mineral sample amounts of 0.01 to 1.0 mg are less than 1 pg U and 20-30 pg Pb. Isotope analysis of the U and Pb from the same filament are carried out using a Finnigan MAT 262 mass-spectrometer in static and dynamic modes. The current analytical level is demonstrated on analyses of international standard zircon 91500 with three different 235U-205Pb and 235U-208Pb isotope tracers and whole rock standards. Results of analyses of two zircon samples are also presented.Os procedimentos analíticos para análises U-Pb por diluição isotópica no Laboratório de Geologia Isotópica (Pará-Iso da Universidade Federal do Pará (UFPA são descritos detalhadamente. Esses procedimentos são aplicados para análises de zircão, titanita, rutilo, apatita, columbita-tantalita e rocha total. A purificação dos reagentes e os procedimentos químicos são feitos em salas limpas. As amostras são dissolvidas em microcápsulas de Teflon em bombas do tipo Parr InstrumentTM. U e Pb são separados em colunas com resina de troca iônica AG 1x8. Os brancos de procedimento para amostra típica(0,01-1 mg são menores que 1 pg de U e 20-30 pg de Pb. As análises isotópicas de Pb e de U são feitas em um único filamento de Re em um espectrômetro de massa Finnigan MAT 262 nos modos estático e dinâmico. O nível analítico atual é comprovado pelas análises do padrão internacional de zircão 91500, usando tr

  3. Study of the Lead Source in the Surrounding Soil of the Lead-zinc Smelters by Isotope Tracing%铅锌冶炼厂周边土壤铅源的铅同位素示踪

    Institute of Scientific and Technical Information of China (English)

    于凯; 李旭祥; 支泽林; 王海波; 郑刘孙

    2014-01-01

    Taken the soil samples nearby a lead-zinc smelter as the research object,the lead content of the lead-zinc ore,the metallurgical coal and the nearby soil were detected.It was concluded that lead content in the soil surrounding the lead-zinc smelter varied from 22.73 mg/kg to 126.51 mg/kg,and the average content was 42.68 mg/kg which was higher by a factor of 1.85 than the local soil background level.Meanwhile the possible contamination sources were analyzed by means of the spatial variability analysis and the lead isotope mixed model formula.It was concluded that the spatial distribution of soil heavy metal nearby the lead-zinc smelter and the lead isotope rates were close to the metallurgical coal and so that the metallurgical coal was the largest contribu-tion to the soil pollution.%以某铅锌冶炼厂周边土壤为研究对象,通过对其原料及周边土壤中铅含量的检测,结果显示:该冶炼厂周边土壤铅质量比在22.73 mg/kg~126.51 mg/kg之间,平均值为42.68 mg/kg,是当地土壤铅背景值的1.85倍。采用铅质量比空间分布分析和同位素混合模型计算分析了冶炼厂周边土壤中铅的可能来源,分析表明:土壤铅质量比的空间分布及铅同位素比值与冶炼厂的焦化原料煤相近,焦化原料煤对周边土壤铅污染贡献最大。

  4. Using biochemical and isotope geochemistry to understand the environmental and public health implications of lead pollution in the lower Guadiana River, Iberia: a freshwater bivalve study.

    Science.gov (United States)

    Company, R; Serafim, A; Lopes, B; Cravo, A; Shepherd, T J; Pearson, G; Bebianno, M J

    2008-11-01

    Lead is a natural component of aquatic ecosystems with no known biological role and is highly toxic. Its toxicity stems from its ability to mimic biologically important metals and to produce membrane damage through lipid peroxidation (LPO). Most lead poisoning symptoms are thought to occur by interfering with an essential enzyme, delta-aminolevulinic acid dehydratase (ALAD), the activity of which is markedly inhibited by lead. The purpose of this work was to study the levels and effects of lead pollution (responses of ALAD and oxidative stress biomarker LPO) in the freshwater bivalve Corbicula fluminea along the lower Guadiana River (Portugal and Spain); a major river system impacted by historic mining pollution and more recent anthropogenic inputs. The results show that the enzymatic activity of ALAD is negatively correlated with the total Pb concentration of the whole tissue suggesting that ALAD has considerable potential as a biomarker of lead exposure in C. fluminea. To identify the sources of lead to which bivalves have been exposed, high precision (206)Pb/(204)Pb, (207)Pb/(204)Pb, (208)Pb/(204)/Pb ratios for C. fluminea confirm that historical mining activities in the Iberian Pyrite Belt are the dominant source of lead pollution in the lower Guadiana River. The isotope patterns however exhibit marked seasonal and geographic variation in response to rainfall and river water management. Locally, other anthropogenic sources of lead have been detected in C. fluminea close to population centres, thus adding to its versatility as a freshwater bio-indicator. Overall, the study highlights the value of natural ecosystems as monitors of water quality and their importance for public health assessment and surveillance.

  5. Anthropogenic and natural lead isotopes in Fe-hydroxides and Fe-sulphates in a watershed associated with arsenic-enriched groundwater, Maine, USA

    Science.gov (United States)

    Ayuso, Robert A.; Foley, Nora K.

    2008-01-01

    A survey of the natural and anthropogenic sources of lead contributing to secondary minerals in sulphidic schists associated with arsenic-enriched groundwater in Coastal Maine shows that the most likely source is natural Pb, particularly from coexisting sulphide minerals. The secondary minerals also reflect notable contributions from anthropogenic Pb. The Pb isotopes establish pathways by which Pb, and by inference As, could have been transported from As-bearing minerals (arsenian pyrite, arsenopyrite, lollingite, orpiment, arsenic oxide and others), via sulphide oxidation or carbonation reactions into multiple generations of secondary minerals (goethite, hematite, jarosite, natrojarosite and others). Lead isotopic compositions of the sulphides and secondary minerals determined by thermal ionization mass spectrometry (n=53) range widely. Lead and As contents of the sulphides and secondary minerals overlap, and are generally positively correlated. Pyrite, the dominant sulphide in sulphidic schists associated with As-enriched groundwater in Coastal Maine, has values of 206Pb/204Pb from 18.186 to 18.391, 207Pb/204Pb from 15.617 to 15.657, 208Pb/204Pb from 38.052 to 38.210, 206Pb/207Pb from c. 1.1625 to 1.1760 and 208Pb/207Pb from c. 2.4276 to 2.4394. Mixtures of Fe-hydroxide and oxide minerals (predominantly goethite and hematite) and secondary Fe-sulphate minerals (jarosite, natrojarosite, rozenite and melanterite) in the sulphidic schists have overlapping but generally higher values of 206Pb/204Pb from 18.495 to 19.747 (one sample at 21.495), 207Pb/204Pb from 15.595 to 15.722 (one sample at 15.839), 208Pb/204Pb from 38.186 to 39.162,206Pb/207Pb from c.1.1860 to 1.2575 (one sample at 1.3855) and 208Pb/207Pb from c. 2.4441 to 2.4865 than the sulphides. Sulphides from Zn-Pb metal mines are somewhat less radiogenic than sulphides from the schists. Other sulphides (mostly pyrite) associated with pegmatites and granitic rocks are heterogeneous and more

  6. Rapid and precise measurement of serum branched-chain and aromatic amino acids by isotope dilution liquid chromatography tandem mass spectrometry.

    Directory of Open Access Journals (Sweden)

    Ruiyue Yang

    Full Text Available BACKGROUND: Serum branched-chain and aromatic amino acids (BCAAs and AAAs have emerged as predictors for the future development of diabetes and may aid in diabetes risk assessment. However, the current methods for the analysis of such amino acids in biological samples are time consuming. METHODS: An isotope dilution liquid chromatography tandem mass spectrometry (ID-LC/MS/MS method for serum BCAAs and AAAs was developed. The serum was mixed with isotope-labeled BCAA and AAA internal standards and the amino acids were extracted with acetonitrile, followed by analysis using LC/MS/MS. The LC separation was performed on a reversed-phase C18 column, and the MS/MS detection was performed via the positive electronic spray ionization in multiple reaction monitoring mode. RESULTS: Specific analysis of the amino acids was achieved within 2 min. Intra-run and total CVs for the amino acids were less than 2% and 4%, respectively, and the analytical recoveries ranged from 99.6 to 103.6%. CONCLUSION: A rapid and precise method for the measurement of serum BCAAs and AAAs was developed and may serve as a quick tool for screening serum BCAAs and AAAs in studies assessing diabetes risk.

  7. Precision mass measurements for studies of nucleosynthesis via the rapid neutron-capture process Penning-trap mass measurements of neutron-rich cadmium and caesium isotopes

    CERN Document Server

    AUTHOR|(CDS)2085660; Litvinov, Yuri A.; Kreim, Susanne

    Although the theory for the rapid neutron-capture process (r-process) was developed more than 55 years ago, the astrophysical site is still under a debate. Theoretical studies predict that the r-process path proceeds through very neutron-rich nuclei with very asymmetric proton- to-neutron ratios. Knowledge about the properties of neutron-rich isotopes found in similar regions of the nuclear chart and furthermore suitable for r-process studies is still little or even not existing. The basic nuclear properties such as binding energies, half-lives, neutron-induced or neutron-capture reaction cross-sections, play an important role in theoretical simulations and can vary or even drastically alternate results of these studies. Therefore, a considerable effort was put forward to access neutron-rich isotopes at radioactive ion-beam facilities like ISOLDE at CERN. The goal of this PhD thesis is to describe the experimental work done for the precision mass measurements of neutron-rich cadmium (129−131 Cd) and caesium...

  8. A high-resolution stalagmite O-C isotope record from Nan-jing and its rapid response to climatic events

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Here we discussed rapid response of the cave temperature and vegetation to the four Dansgaard-Oeschger cold and warm cycles during 50-40 kaBP based on results of oxygen and carbon stable isotopic compositions from a stalagmite in Tangshan, Nanjing. It is found that the amount of C3 vegetation relative to C4-type declines during the D-O warm events, indicating the decrease of the effective meteoric precipitation. Compared with O-isotope records of the Greenland ice core, the stalagmite record displays a very similar pattern to Greenland ice core record over the decade-century time scale, suggesting that the changes of the East Asian monsoon climate are in accordance with the high-latitude polar climate in the short-term time scale. The age of the ice-rafted H5 event in the stalagmite record, however, preceded that of Greenland ice cores by 2 ka. This out of phase between the remote areas cannot be yet proven because the two time scales were determined from different dating methods.``

  9. Actin dynamics is rapidly regulated by the PTEN and PIP2 signaling pathways leading to myocyte hypertrophy.

    Science.gov (United States)

    Li, Jieli; Tanhehco, Elaine J; Russell, Brenda

    2014-12-01

    Mature cardiac myocytes are terminally differentiated, and the heart has limited capacity to replace lost myocytes. Thus adaptation of myocyte size plays an important role in the determination of cardiac function. The hypothesis tested is that regulation of the dynamic exchange of actin leads to cardiac hypertrophy. ANG II was used as a hypertrophic stimulant in mouse heart and neonatal rat ventricular myocytes (NRVMs) in culture for assessment of a mechanism for regulation of actin dynamics by phosphatidylinositol 4,5-bisphosphate (PIP2). Actin dynamics in NRVMs rapidly increased in a PIP2-dependent manner, measured by imaging and fluorescence recovery after photobleaching (FRAP). A significant increase in PIP2 levels was found by immunoblotting in both adult mouse heart tissue and cultured NRVMs. Inhibition of phosphatase and tensin homolog (PTEN) in NRVMs markedly blunted ANG II-induced increases in actin dynamics, the PIP2 level, and cell size. Furthermore, PTEN activity was dramatically upregulated in ANG II-treated NRVMs but downregulated when PTEN inhibitors were used. The time course of the rise in the PIP2 level was inversely related to the fall in the PIP3 level, which was significant by 30 min in ANG II-treated NRVMs. However, significant translocation of PTEN to the plasma membrane occurred by 10 min, suggesting a crucial initial step for PTEN for the cellular responses to ANG II. In conclusion, PTEN and PIP2 signaling may play an important role in myocyte hypertrophy by the regulation of actin filament dynamics, which is induced by ANG II stimulation. Copyright © 2014 the American Physiological Society.

  10. Assessment of heavy metal pollution in sediments from Xiangjiang River (China) using sequential extraction and lead isotope analysis

    Institute of Scientific and Technical Information of China (English)

    蒋博峰; 孙卫玲

    2014-01-01

    The heavy metal (such as Cr, Ni, Cu, Cd, Pb, and Zn) concentration, speciation, and pollution source in 43 sediment samples from the Xiangjiang River were investigated using sequential extraction combined with Pb isotope analysis. Cu, Cd, Pb, and Zn concentrations are higher than their background values, while Cr and Ni concentrations are close to those. Sequential extraction demonstrates that heavy metals have different fractions, showing different bioavailabilities. Thew(206Pb)/w(207Pb) ratio increases with decreasing bioavailability in the order of exchangeable

  11. A century long sedimentary record of anthropogenic lead (Pb), Pb isotopes and other trace metals in Singapore.

    Science.gov (United States)

    Chen, Mengli; Boyle, Edward A; Switzer, Adam D; Gouramanis, Chris

    2016-06-01

    Reconstructing the history of metal deposition in Singapore lake sediments contributes to understanding the anthropogenic and natural metal deposition in the data-sparse Southeast Asia. To this end, we present a sedimentary record of Pb, Pb isotopes and eleven other metals (Ag, As, Ba, Cd, Co, Cr, Cu, Ni, Tl, U and Zn) from a well-dated sediment core collected near the depocenter of MacRitchie Reservoir in central Singapore. Before the 1900s, the sedimentary Pb concentration was less than 2 mg/kg for both soil and sediment, with a corresponding (206)Pb/(207)Pb of ∼1.20. The Pb concentration increased to 55 mg/kg in the 1990s, and correspondingly the (206)Pb/(207)Pb decreased to less than 1.14. The (206)Pb/(207)Pb in the core top sediment is concordant with the (206)Pb/(207)Pb signal of aerosols in Singapore and other Southeast Asian cities, suggesting that Pb in the reservoir sediment was mainly from atmospheric deposition. Using the Pb concentration in the topmost layer of sediment, the estimated atmospheric Pb flux in Singapore today is ∼1.6 × 10(-2) g/m(2) yr. The concentrations of eleven other metals preserved in the sediment were also determined. A principal component analysis showed that most of the metals exhibit an increasing trend towards 1990s with a local concentration peak in the mid-20(th) century.

  12. Stable isotope probing and dynamic loading experiments provide insight into the ecophysiology of novel ammonia oxidizers in rapid gravity sand filters

    DEFF Research Database (Denmark)

    Fowler, Jane; Palomo, Alejandro; Gülay, Arda

    to elucidate the differences in ecophysiology between the ammonia oxidizing clades that enable them to co-exist in this unique environment. Experiments were conducted using sand columns designed and operated to mimic the conditions in the full-scale parent RSF. RNA and DNA stable isotope probing based on 13C......Nitrification is often the dominant microbial process in rapid gravity sand filters (RSF), used to treat aerated groundwater to produce drinking water. RSFs harbor diverse microbial communities including a range of ammonia oxidizing clades; Betaproteobacteria (Nitrosomonas, Nitrosospira), Archaea......, diverse potentially ammonia oxidizing heterotrophs and abundant Nitrospira spp., recently shown to comprise both canonical nitrite oxidizing as well as complete ammonium oxidizing (comammox) types. We examined the contributions of the different ammonia oxidizers to in situ ammonia oxidation, and aimed...

  13. Lead isotope ratios in lichen samples evaluated by ICP-ToF-MS to assess possible atmospheric pollution sources in Havana, Cuba.

    Science.gov (United States)

    Alvarez, Alfredo Montero; Estévez Alvarez, Juan R; do Nascimento, Clístenes Williams Araújo; González, Iván Pupo; Rizo, Oscar Díaz; Carzola, Lázaro Lima; Torres, Roberto Ayllón; Pascual, Jorge Gómez

    2017-01-01

    Epiphytic lichens, collected from 119 sampling sites grown over "Roistonea Royal Palm" trees, were used to assess the spatial distribution pattern of lead (Pb) and identify possible pollution sources in Havana (Cuba). Lead concentrations in lichens and topsoils were determined by flame atomic absorption spectrophotometry and inductively coupled plasma (ICP) atomic emission spectrometry, respectively, while Pb in crude oils and gasoline samples were measured by ICP-time of flight mass spectrometry (ICP-ToF-MS). Lead isotopic ratios measurements for lichens, soils, and crude oils were obtained by ICP-ToF-MS. We found that enrichment factors (EF) reflected a moderate contamination for 71% of the samples (EF > 10). The (206)Pb/(207)Pb ratio values for lichens ranged from 1.17 to 1.20 and were a mixture of natural radiogenic and industrial activities (e.g., crude oils and fire plants). The low concentration of Pb found in gasoline (<7.0 μg L(-1)) confirms the official statement that leaded gasoline is no longer used in Cuba.

  14. Multivariate statistical and lead isotopic analyses approach to identify heavy metal sources in topsoil from the industrial zone of Beijing Capital Iron and Steel Factory.

    Science.gov (United States)

    Zhu, Guangxu; Guo, Qingjun; Xiao, Huayun; Chen, Tongbin; Yang, Jun

    2017-06-01

    Heavy metals are considered toxic to humans and ecosystems. In the present study, heavy metal concentration in soil was investigated using the single pollution index (PIi), the integrated Nemerow pollution index (PIN), and the geoaccumulation index (Igeo) to determine metal accumulation and its pollution status at the abandoned site of the Capital Iron and Steel Factory in Beijing and its surrounding area. Multivariate statistical (principal component analysis and correlation analysis), geostatistical analysis (ArcGIS tool), combined with stable Pb isotopic ratios, were applied to explore the characteristics of heavy metal pollution and the possible sources of pollutants. The results indicated that heavy metal elements show different degrees of accumulation in the study area, the observed trend of the enrichment factors, and the geoaccumulation index was Hg > Cd > Zn > Cr > Pb > Cu ≈ As > Ni. Hg, Cd, Zn, and Cr were the dominant elements that influenced soil quality in the study area. The Nemerow index method indicated that all of the heavy metals caused serious pollution except Ni. Multivariate statistical analysis indicated that Cd, Zn, Cu, and Pb show obvious correlation and have higher loads on the same principal component, suggesting that they had the same sources, which are related to industrial activities and vehicle emissions. The spatial distribution maps based on ordinary kriging showed that high concentrations of heavy metals were located in the local factory area and in the southeast-northwest part of the study region, corresponding with the predominant wind directions. Analyses of lead isotopes confirmed that Pb in the study soils is predominantly derived from three Pb sources: dust generated during steel production, coal combustion, and the natural background. Moreover, the ternary mixture model based on lead isotope analysis indicates that lead in the study soils originates mainly from anthropogenic sources, which contribute much more

  15. Pre-Hercynian hydrothermalism in South Iberia: lead isotope geochemistry constraints; Hydrothermalisme ante-hercynien en Sud-Iberie: apport de la geochimie isotopique du plomb

    Energy Technology Data Exchange (ETDEWEB)

    Marcoux, E.; Onezime, J. [Orleans Univ., Institut des Sciences de la Terre d' Orleans, 45 (France); Pascual, E. [Universite d' Huelva, Dept. de Geologia y MIneria, Huelva (Spain)

    2002-04-01

    Lead isotope study has been performed on massive sulphide deposits of Ossa-Morena and Aracena Belt (South Iberia). Results suggest the existence of at least two ancient hydrothermal events. The first one, Upper Brioverian in age ({approx}600-570 Ma), gave birth to Maria-Luisa and Puebla de la Reina massive sulphide deposits; it thus confirms the existence of a Cadomian orogen in South Iberia. Isotopic compositions indicate a local contribution of mantle-derived material (Maria Luisa mine), confirming the presence of ancient oceanic crust in Aracena Belt. This mineralizing event seems to extend till the Armorican Massif. The second episode, Eo-Hercynian in age ({approx}400-350 Ma) has allowed genesis of massive sulphide deposits of la Nava Paredon and Aguas Blancas, and could be coeval with the emplacement of South-Iberian massive sulphide ore deposits in the neighbouring South-Portuguese Zone. A more continental crustal source for later ore deposits could explain the much more important metal accumulation in this zone. (authors)

  16. Rapid determination of (237)Np and plutonium isotopes in urine by inductively-coupled plasma mass spectrometry and alpha spectrometry.

    Science.gov (United States)

    Maxwell, Sherrod L; Culligan, Brian K; Jones, Vernon D; Nichols, Sheldon T; Noyes, Gary W; Bernard, Maureen A

    2011-08-01

    A new rapid separation method was developed for the measurement of plutonium and neptunium in urine samples by inductively-coupled plasma mass spectrometry (ICP-MS) and/or alpha spectrometry with enhanced uranium removal. This method allows separation and preconcentration of plutonium and neptunium in urine samples using stacked extraction chromatography cartridges and vacuum box flow rates to facilitate rapid separations. There is an increasing need to develop faster analytical methods for emergency response samples. There is also enormous benefit to having rapid bioassay methods in the event that a nuclear worker has an uptake (puncture wound, etc.) to assess the magnitude of the uptake and guide efforts to mitigate dose (e.g., tissue excision and chelation therapy). This new method focuses only on the rapid separation of plutonium and neptunium with enhanced removal of uranium. For ICP-MS, purified solutions must have low salt content and low concentration of uranium due to spectral interference of (238)U(1)H(+) on m/z 239. Uranium removal using this method is enhanced by loading plutonium and neptunium initially onto TEVA resin, then moving plutonium to DGA resin where additional purification from uranium is performed with a decontamination factor of almost 1×10(5). If UTEVA resin is added to the separation scheme, a decontamination factor of ~3 × 10(6) can be achieved.

  17. Contamination limits for real and personal property. Progress report, July--December 1975. [Plutonium and lead isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Healy, J.W.; Wenzel, W.J.

    1976-05-01

    Studies of surface contamination continued with an attempt to apply previous concepts. Revision of the proposed limit for plutonium in soils was started with major efforts on wind resuspension and the use of data on environmental lead to estimate intake by children.

  18. Soils Developed from Different Volcanic Rocks from the Fernando de Noronha Island: Rare-Earth Element Patterns and Isotopic Lead Composition

    Directory of Open Access Journals (Sweden)

    Sonia Maria Barros de Oliveira

    2011-12-01

    Full Text Available This study examines the infl uence of pedogenesis on the distribution of rare earth elements in soils derived fromdifferent rock types and formed under tropical humid climate, as well as the possible contribution of airborne Pb to thesesoils. We studied 5 soil profi les developed from different volcanic rocks cropping out in the Fernando de Noronha island.Results show that in the course of weathering, the soils were enriched in REE. The REE patterns of the soils are similarto those of the parent material, except for a slight HREE enrichment. Lead-isotope data indicate the presence of a nonradiogenicanthropogenic component in the upper horizons of the soil profi les.

  19. Precambrian ophiolites of Arabia; a summary of geologic settings, U-Pb geochronology, lead isotope characteristics, and implications for microplate accretion, Kingdom of Saudi Arabia

    Science.gov (United States)

    Pallister, John S.; Stacey, J.S.; Fischer, L.B.; Premo, W.R.

    1988-01-01

    Disrupted ophiolites occur in linear belts as much as 900 km long between micro plates that collided during the late Proterozoic to form the Arabian Shield. The U-Pb zircon ages and lead-isotope data from these ophiolitic rocks help constrain the history of accretion of the Arabian Shield and thereby contribute to the definition of its microplates and terranes. Microplates of the central and western Arabian Shield are generally thought to represent intra-oceanic island arcs that range in age from about 900 Ma to 640 Ma; however, a region of the eastern Arabian Shield contains rocks of early Proterozoic age and may represent an exotic continental fragment entrained between the arc complexes.

  20. 铅稳定同位素示踪在铅污染研究中的应用%Application of stable lead isotopes to trace the lead pollution

    Institute of Scientific and Technical Information of China (English)

    常向阳; 付善明; 陈南; 吴丽琴; 毛利红; 王道芳; 肖方; 朱炳泉

    2012-01-01

    The history of human civilization is also the annals of lead pollution. The wide use of lead results in the lead pollution of atmosphere, water and surface sediments globally. Lots of harm issues to human health draw our attention to the lead pollution. Due to various sources, it is a complicated problem how to identify the source of the lead pollution and evaluate the extent of the lead pollution. There are lots of evidence indicating that the ratios of lead isotopes could trace the sources of lead pollution effectively and estimate trace out of the moving path of the industrial waste in large scale. With the use of lead-free gasoline popularly, the lead pollu- tion from the gasoline and food becomes less and less than before, but that from the paint should be paid more attention to.%人类文明史也是一部铅污染史,铅的广泛使用产生了全球性的大气、水源和地表沉积物的铅污染.铅污染造成对人体健康的危害问题已引起社会的广泛关注.铅的污染来源是多方面的,对于如何来定量确定污染源和评估污染程度仍然是一个复杂的问题.铅同位素组成特征可以有效地指示污染的来源,并可有效地评价大尺度范围内工业污染物的运移路径.随着无铅汽油的广泛使用,来源于汽油和食物中的铅污染在减弱,但来源于涂料和油漆中的铅污染越来越受到关注.

  1. Characterization of rapid climate changes through isotope analyses of ice and entrapped air in the NEEM ice core

    DEFF Research Database (Denmark)

    Guillevic, Myriam

    Greenland ice core have revealed the occurrence of rapid climatic instabilities during the last glacial period, known as Dansgaard-Oeschger (DO) events, while marine cores from the North Atlantic have evidenced layers of ice rafted debris deposited by icebergs melt, caused by the collapse...... of Northern hemisphere ice sheets, known as Heinrich events. The imprint of DO and Heinrich events is also recorded at mid to low latitudes in different archives of the northern hemisphere. A detailed multi-proxy study of the sequence of these rapid instabilities is essential for understanding the climate...... mechanisms at play. Recent analytical developments have made possible to measure new paleoclimate proxies in Greenland ice cores. In this thesis we first contribute to these analytical developments by measuring the new innovative parameter 17O-excess at LSCE (Laboratoire des Sciences du Climatet de l...

  2. Application of inductively coupled plasma quadrupole mass spectrometry for the determination of monazite ages by lead isotope ratios

    OpenAIRE

    Godoy,José Marcus; Godoy,Maria Luiza D. P; Aronne,Cláudia C.

    2007-01-01

    In order to evaluate the applicability of inductively coupled plasma quadrupole mass spectrometry to the determination of Pb/Pb, U/Pb and Th/Pb ages of monazite, studies were carried out initially applying lead atom ratio reference standards (NIST SRM 981 and 982). Further, the optimized methodology was applied to monazite sands from three different sites, Sugar Loaf Hill (Rio de Janeiro city), Buena (Rio de Janeiro state) and Black Sands Beach (Guarapari, Espirito Santo state); the obtained ...

  3. Combining lead isotopes and cluster analysis to distinguish the Guarani and Serra Geral Aquifer Systems and contaminated waters in a highly industrialized area in Southern Brazil.

    Science.gov (United States)

    Kuhn, Isadora Aumond; Roisenberg, Ari

    2017-10-01

    The Rio dos Sinos Watershed area is located at the Middle-West region of the Rio Grande do Sul State, Southern Brazil, along thirty two municipalities and affecting 1.5 million inhabitants and many important industrial centers. Three main aquifers are recognized in the study area: the unconfined-fractured Serra Geral Aquifer System, the porous Guarani Aquifer System, and the Permian Aquitard. This study aims to understand groundwater, surface water and human activity interactions in the Rio dos Sinos Watershed, evaluating the application of stable lead isotopic ratios analyzed for this propose. Thirty six groundwater samples, 8 surface water samples and 5 liquid effluents of tanneries and landfills samples were measured using a Thermal Ionization Mass Spectrometer Thermo-Finnigan and a Neptune Multi-Collector Inductively Coupled Plasma Mass Spectrometer. Groundwater isotopic ratios have a wider range compared to the surface water, with less radiogenic averages (208)Pb/(204)Pb = 38.1837 vs 38.4050 (standard deviation = 0.2921 vs 0.1343) and (206)Pb/(204)Pb = 18.2947 vs 18.4766 (standard deviation = 0.2215 vs 0.1059), respectively. Industrial liquid effluents (tanneries and industrial landfill) have averages (208)Pb/(204)Pb = 38.1956 and (206)Pb/(204)Pb = 18.3169, distinct from effluent samples of domestic sanitary landfill (averages (208)Pb/(204)Pb = 38.2353 and (206)Pb/(204)Pb = 18.6607). Hierarchical cluster analysis led to distinguish six groups of groundwater, representing the three aquifers that occur in the area, two clusters suggesting groundwater mixtures and one demonstrating a highly contaminated groundwater. By analyzing the cluster results and wells' stratigraphic profiles it was possible to distinguish the different aquifers in the area. The Serra Geral Aquifer System has (206)Pb/(204)Pb ratios between 18.4718 and 18.7089; (207)Pb/(204)Pb between 15.6692 and 15.6777; (208)Pb/(204)Pb between 38.6826 and 38.7616; (207)Pb/(206)Pb between 0

  4. Cochrane Rapid Reviews Methods Group to play a leading role in guiding the production of informed high-quality, timely research evidence syntheses.

    Science.gov (United States)

    Garritty, Chantelle; Stevens, Adrienne; Gartlehner, Gerald; King, Valerie; Kamel, Chris

    2016-10-28

    Policymakers and healthcare stakeholders are increasingly seeking evidence to inform the policymaking process, and often use existing or commissioned systematic reviews to inform decisions. However, the methodologies that make systematic reviews authoritative take time, typically 1 to 2 years to complete. Outside the traditional SR timeline, "rapid reviews" have emerged as an efficient tool to get evidence to decision-makers more quickly. However, the use of rapid reviews does present challenges. To date, there has been limited published empirical information about this approach to compiling evidence. Thus, it remains a poorly understood and ill-defined set of diverse methodologies with various labels. In recent years, the need to further explore rapid review methods, characteristics, and their use has been recognized by a growing network of healthcare researchers, policymakers, and organizations, several with ties to Cochrane, which is recognized as representing an international gold standard for high-quality, systematic reviews. In this commentary, we introduce the newly established Cochrane Rapid Reviews Methods Group developed to play a leading role in guiding the production of rapid reviews given they are increasingly employed as a research synthesis tool to support timely evidence-informed decision-making. We discuss how the group was formed and outline the group's structure and remit. We also discuss the need to establish a more robust evidence base for rapid reviews in the published literature, and the importance of promoting registration of rapid review protocols in an effort to promote efficiency and transparency in research. As with standard systematic reviews, the core principles of evidence-based synthesis should apply to rapid reviews in order to minimize bias to the extent possible. The Cochrane Rapid Reviews Methods Group will serve to establish a network of rapid review stakeholders and provide a forum for discussion and training. By facilitating

  5. Does Rapid and Sustained Economic Growth Lead to Convergence in Health Resources: The Case of China From 1980 to 2010

    National Research Council Canada - National Science Library

    Liang, Di; Zhang, Donglan; Huang, Jiayan; Schweitzer, Stuart

    2016-01-01

    China’s rapid and sustained economic growth offers an opportunity to ask whether the advantages of growth diffuse throughout an economy, or remain localized in areas where the growth has been the greatest...

  6. Characterization of rapid climate changes through isotope analyses of ice and entrapped air in the NEEM ice core

    DEFF Research Database (Denmark)

    Guillevic, Myriam

    Greenland ice core have revealed the occurrence of rapid climatic instabilities during the last glacial period, known as Dansgaard-Oeschger (DO) events, while marine cores from the North Atlantic have evidenced layers of ice rafted debris deposited by icebergs melt, caused by the collapse...... four Greenland deep ice cores (GRIP, GISP2, NGRIP and NEEM) are investigated over a series of Dansgaard– Oeschger events (DO 8, 9 and 10). Combined with firn modeling, δ15N data allow us to quantify abrupt temperature increases for each drill site (1σ = 0.6°C for NEEM, GRIP and GISP2, 1.5°C for NGRIP...

  7. Investigation of Analytical Techniques for the Rapid Determination of the Moisture Content of NOL 130 Primer Mix and Lead Azide

    Science.gov (United States)

    1986-05-01

    the presence of NOL 130 6 Determination of moisture content of dextrinated lead azide 14 containing known amounts of water, by the Karl Fisher method...maLhiod, extraction mode 8 Determinatiov) of moisture content of special purpose and 16 dextrinated lead atide, containing known amounts of water by the...water in special purpose and dextrinated lead azides were determined by the method described in the experimen- tal section of this report, data shown

  8. Rapid Determination of 226Ra and Uranium Isotopes in Solid Samples by Fusion with Lithium Metaborate and Alpha Spectrometry

    Directory of Open Access Journals (Sweden)

    R. Bojanowski

    2002-01-01

    Full Text Available A simple and rapid method has been developed to determine 226Ra in rocks, soils, and sediments. Samples are decomposed by fusion with lithium metaborate and the melt is dissolved in a solution containing sulfates and citric acid. During the dissolution, a fine suspension of mixed barium and radium sulfates is formed. The microcrystals are collected on a membrane filter (pore size 0.1 μm and analysed in an alpha spectrometer. Application of a 133Ba tracer enables us to assess the loss of the analyte, which only rarely exceeds 10%. All analytical operations, beginning from sample decomposition to source preparation for alpha spectrometry, can be accomplished within 1 or 2 h.

  9. Rapid Solidification of Sn-Cu-Al Alloys for High-Reliability, Lead-Free Solder: Part I. Microstructural Characterization of Rapidly Solidified Solders

    Science.gov (United States)

    Reeve, Kathlene N.; Choquette, Stephanie M.; Anderson, Iver E.; Handwerker, Carol A.

    2016-12-01

    Particles of Cu x Al y in Sn-Cu-Al solders have previously been shown to nucleate the Cu6Sn5 phase during solidification. In this study, the number and size of Cu6Sn5 nucleation sites were controlled through the particle size refinement of Cu x Al y via rapid solidification processing and controlled cooling in a differential scanning calorimeter. Cooling rates spanning eight orders of magnitude were used to refine the average Cu x Al y and Cu6Sn5 particle sizes down to submicron ranges. The average particle sizes, particle size distributions, and morphologies in the microstructures were analyzed as a function of alloy composition and cooling rate. Deep etching of the samples revealed the three-dimensional microstructures and illuminated the epitaxial and morphological relationships between the Cu x Al y and Cu6Sn5 phases. Transitions in the Cu6Sn5 particle morphologies from faceted rods to nonfaceted, equiaxed particles were observed as a function of both cooling rate and composition. Initial solidification cooling rates within the range of 103 to 104 °C/s were found to be optimal for realizing particle size refinement and maintaining the Cu x Al y /Cu6Sn5 nucleant relationship. In addition, little evidence of the formation or decomposition of the ternary- β phase in the solidified alloys was noted. Solidification pathways omitting the formation of the ternary- β phase agreed well with observed room temperature microstructures.

  10. Uranium-lead isotope systematics and apparent ages of zircons and other minerals in precambrian granitic rocks, Granite Mountains, Wyoming

    Science.gov (United States)

    Ludwig, K. R.; Stuckless, J.S.

    1978-01-01

    Zircon suites from the two main types of granite in the Granite Mountains, Wyoming, yielded concordia-intercept ages of 2,640??20 m.y. for a red, foliated granite (granite of Long Creek Mountain) and 2,595??40 m.y. for the much larger mass of the granite of Lankin Dome. These ages are statistically distinct (40??20 m.y. difference) and are consistent with observed chemical and textural differences. The lower intercepts of the zircon chords of 50??40 and 100+ 75 m.y. for the granite of Long Creek Mountain and granite of Lankin Dome, respectively, are not consistent with reasonable continuous diffusion lead-loss curves but do correspond well with the known (Laramide) time of uplift of the rocks. Epidote, zircon, and apatite from silicified and epidotized zones in the granites all record at least one postcrystallization disturbance in addition to the Laramide event and do not define a unique age of silicification and epidotization. The lower limit of ???2,500 m.y. provided by the least disturbed epidote, however, suggests that these rocks were probably formed by deuteric processes shortly after emplacement of the granite of the Lankin Dome. The earlier of the two disturbances that affected the minerals of the silicified-epidotized rock can be bracketed between 1,350 and 2,240 m.y. ago and is probably the same event that lowered mineral K-Ar and ages in the region. Zircon suites from both types of granite show well-defined linear correlations among U content, common-Pb content, and degree of discordance. One of the zircon suites has an extremely high common-Pb content (up to 180 ppm) and exhibits a component of radiogenic-Pb loss that is apparently unrelated to radiation damage. ?? 1978 Springer-Verlag.

  11. Rapid determination of natural and synthetic hormones in biosolids and poultry manure by isotope dilution GC-MS/MS.

    Science.gov (United States)

    Albero, Beatriz; Sánchez-Brunete, Consuelo; Miguel, Esther; Aznar, Ramón; Tadeo, José L

    2014-04-01

    The release of hormones into the environment due to land application of biosolids and manure is a cause of concern for their potential impacts. This paper presents the development of a rapid and sensitive method, based on extraction, for the analysis of 13 hormones in biosolids and poultry manure. A simultaneous derivatization of hydroxyl and ketone groups was carried out for the determination of hormones by GC–MS/MS. The method was validated in three matrices (sewage sludge, manure, and broiler litter). Recoveries from spiked samples at three concentration levels (50, 25, and 10 ng/g) ranged from 76 to 124% with relative SDs ≤ 16%. Method detection limits for the three matrices were in the range of 0.5–3.0 ng/g dry weight. The optimized method was applied to biosolid and poultry manure samples collected in Spain. Only seven of the 13 studied hormones were detected in the different samples. trans-Androsterone was detected at high levels (up to 3.1 μg/g in biosolid samples). Estrone and estradiol were the two hormones detected at higher levels in layer manure, whereas estrone and 4-androstene-3,17-dione presented the highest levels in broiler litter.

  12. Rapid detection of blaOXA in carbapenem-susceptible Acinetobacter radioresistens bacteremia leading to unnecessary antimicrobial administration.

    Science.gov (United States)

    Brady, Adam C; Lewis, James S; Pfeiffer, Christopher D

    2016-08-01

    Rapid molecular techniques to identify resistant pathogens are revolutionizing antibiotic stewardship; however, it is important to recognize the limitations of these techniques. Herein we describe two cases of bacteremia that were both initially identified by genotypic testing as carbapenem-resistant Acinetobacter spp. and subsequently identified phenotypically as carbapenem-susceptible A. radioresistens. The genotypic results prompted unnecessary broad-spectrum antibiotic use and infection control concerns.

  13. Ecdysteroids Elicit a Rapid Ca2+ Flux Leading to Akt Activation and Increased Protein Synthesis in Skeletal Muscle Cells

    OpenAIRE

    Gorelick-Feldman, Jonathan; Cohick, Wendie; Raskin, Ilya

    2010-01-01

    Phytoecdysteroids, structurally similar to insect molting hormones, produce a range of effects in mammals, including increasing growth and physical performance. In skeletal muscle cells, phytoecdysteroids increase protein synthesis. In this study we show that in a mouse skeletal muscle cell line, C2C12, 20-hydroxyecdysone (20HE), a common phytoecdysteroid in both insects and plants, elicited a rapid elevation in intracellular calcium, followed by sustained Akt activation and increased protein...

  14. Simple and rapid analytical method for detection of amino acids in blood using blood spot on filter paper, fast-GC/MS and isotope dilution technique.

    Science.gov (United States)

    Kawana, Shuichi; Nakagawa, Katsuhiro; Hasegawa, Yuki; Yamaguchi, Seiji

    2010-11-15

    A simple and rapid method for quantitative analysis of amino acids, including valine (Val), leucine (Leu), isoleucine (Ile), methionine (Met) and phenylalanine (Phe), in whole blood has been developed using GC/MS. In this method, whole blood was collected using a filter paper technique, and a 1/8 in. blood spot punch was used for sample preparation. Amino acids were extracted from the sample, and the extracts were purified using cation-exchange resins. The isotope dilution method using ²H₈-Val, ²H₃-Leu, ²H₃-Met and ²H₅-Phe as internal standards was applied. Following propyl chloroformate derivatization, the derivatives were analyzed using fast-GC/MS. The extraction recoveries using these techniques ranged from 69.8% to 87.9%, and analysis time for each sample was approximately 26 min. Calibration curves at concentrations from 0.0 to 1666.7 μmol/l for Val, Leu, Ile and Phe and from 0.0 to 333.3 μmol/l for Met showed good linearity with regression coefficients=1. The method detection limits for Val, Leu, Ile, Met and Phe were 24.2, 16.7, 8.7, 1.5 and 12.9 μmol/l, respectively. This method was applied to blood spot samples obtained from patients with phenylketonuria (PKU), maple syrup urine disease (MSUD), hypermethionine and neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD), and the analysis results showed that the concentrations of amino acids that characterize these diseases were increased. These results indicate that this method provides a simple and rapid procedure for precise determination of amino acids in whole blood. Copyright © 2010 Elsevier B.V. All rights reserved.

  15. Origin of lead in eight Central European peat bogs determined from isotope ratios, strengths, and operation times of regional pollution sources.

    Science.gov (United States)

    Novák, Martin; Emmanuel, Simon; Vile, Melanie A; Erel, Yigal; Véron, Alain; Paces, Tomás; Wieder, R Kelman; Vanecek, Mirko; Stepánová, Markéta; Brízová, Eva; Hovorka, Jan

    2003-02-01

    Lead originating from coal burning, gasoline burning, and ore smelting was identified in 210Pb-dated profiles through eight peat bogs distributed over an area of 60,000 km2. The Sphagnum-dominated bogs were located mainly in mountainous regions of the Czech Republic bordering with Germany, Austria, and Poland. Basal peat 14C-dated at 11,000 years BP had a relatively high 206Pb/207Pb ratio (1.193). Peat deposited around 1800 AD had a lower 206Pb/207Pb ratio of 1.168-1.178, indicating that environmental lead in Central Europe had been largely affected by human activity (smelting) even before the beginning of the Industrial Revolution. Five of the sites exhibited a nearly constant 206Pb/207Pb ratio (1.175) throughout the 19th century, resembling the "anthropogenic baseline" described in Northern Europe (1.17). At all sites, the 206Pb/207Pb ratio of peat decreased at least until 1980; at four sites, a reversal to more radiogenic values (higher 206Pb/207Pb), typical of easing pollution, was observed in the following decade (1980-1990). A time series of annual outputs for 14 different mining districts dispersing lead into the environment has been constructed for the past 200 years. The production of Ag-Pb, coal, and leaded gasoline peaked in 1900, 1980, and 1980, respectively. In contrast to other European countries, no peak in annual Pb accumulation rates was found in 1900, the year of maximum ore smelting. The highest annual Pb accumulation rates in peat were consistent with the highest Pb emission rates from coal-fired power plants and traffic (1980). Although maximum coal and gasoline production coincided in time, their isotope ratios were unique. The mean measured 206Pb/207Pb ratios of local coal, ores, and gasoline were 1.19, 1.16, and 1.11, respectively. A considerable proportion of coal emissions, relative to gasoline emisions, was responsible for the higher 206Pb/207Pb ratios in the recent atmosphere (1.15) compared to Western Europe (1.10). As in West European

  16. Rapid Synthesis of Lead Oxide Nanorods by One-step Solid-state Chemical Reaction at Room Temperature

    Institute of Scientific and Technical Information of China (English)

    CAO, Ya-Li(曹亚丽); JIA, Dian-Zeng(贾殿赠); LIU, Lang(刘浪); LUO, Jian-Min(骆建敏)

    2004-01-01

    A simple and facile method was reported to synthesize lead oxide nanorods. Nanorods of lead oxide were obtained directly from grinding solid metal salt and sodium hydroxide in agate mortar with the assistance of a suitable nonionic surfactant in only one step, which is different from the result of hydroxide in solution. The product has been characterized by XRD, TEM and SEM. The formation mechanism of rod-like morphology is discussed and the surfactant plays an important soft-template role in modifying the interface of solid-state reaction and according process of rod-formation.

  17. Behaviour mechanisms and correlation between lead (Pb) and its isotope (210)Pb in industrial residue as an indicator for waste characterization.

    Science.gov (United States)

    Vaasma, Taavi; Bityukova, Liidia; Kiisk, Madis; Özden, Banu; Tkaczyk, Alan Henry

    2016-12-01

    Total lead and (210)Pb concentrations were determined in various ash fractions (collected from two of the world's largest oil shale-fired power plants) by inductively coupled plasma mass-spectrometry (ICP-MS) and gamma spectrometry. Results show a clear increase in total lead (values up to 193 ppm in filter ashes) and (210)Pb (values up to 148 Bq kg(-1) in filter ashes) concentrations in the ash fractions from the furnace towards the filter ashes. A strong positive linear correlation (Pearson's bivariate correlation remained between 0.86 and 0.99) was determined between total lead concentration (ppm) and (210)Pb activity concentration (Bq kg(-1)) within all the boilers under observation. The constant concentration ratio between total lead and (210)Pb remained around one (with minor exceptions), independent of the sampling location and the used combustion technology. The determined concentration ratio can be applicable as an indicative tool in waste material characterization. It also provides multiple additions to the general material characterization approach, by integrating radiological and elemental studies and providing an option to rapidly obtain initial indicative information about the residues. This in turn helps to generate the initial information to work out the next steps in waste material management.

  18. Isotope analysis of lead pollution sources in wheat kernel%小麦籽粒铅污染来源的同位素解析研究

    Institute of Scientific and Technical Information of China (English)

    赵多勇; 魏益民; 魏帅; 郭波莉; 蔡先峰; 吴小胜

    2012-01-01

    以中国西北地区某工业区为研究区域,采集大气降尘、耕层土壤样品(0~20 cm),及对应农田位置的小麦籽粒样品,用电感耦合等离子质谱( ICP-MS)测定铅元素质量比及铅同位素比率值.运用普通块克里金法(Ordinary Kriging)预测大气铅沉降通量分布、耕层土壤和小麦籽粒铅质量比空间分布;结合二元混合模型计算各污染源对小麦籽粒铅质量比的贡献率.结果表明:1)耕层土壤铅质量比范围为21.8~40.0 mg/kg,平均值为27.1 mg/kg,高于当地土壤背景值(21.4 mg/kg),说明耕层土壤受到一定程度的污染.2)研究区域小麦籽粒铅质量比范围为0.269~0.768 mg/kg,平均值为0.430 mg/kg,超标率达100%.3)大气降尘和耕层土壤对小麦籽粒铅质量比的贡献率分别为90%~99%和1%~10%.通过研究耕层土壤和小麦铅污染的范围及程度,探讨小麦籽粒铅污染的来源,解析各污染源的相对贡献率,可为制定控制食品中重金属污染,保障食品安全措施提供依据.%To identify and apportion the contributions of lead pollution sources in wheat kernel,the surrounding area of a lead-zinc smelter in northwestern China was taken as the study area,local atmospheric deposits,tilled soils (0-20 cm),and the corresponding wheat samples were collected and then lead concentrations and isotope ratios was analyzed by ICP-MS . The spatial distribution of atmospheric lead settlement fluxes as well as lead concentrations in soil and wheat kernel were predicted by Ordinary Krigging methods. The contributions of lead pollution sources to wheat kernel were calculated with a linear mixing model. The results showed that lead concentrations in tilled soil ranged from 21.8 to 40.0 mg/kg,and the average level (27.1 mg/kg) was higher than background value (21.4 mg/kg) of local soil samples,which indicated that the soil in local area was polluted slightly. The lead concentrations of wheat kernel in the canyon ranged 0

  19. Identification and Decay Studies of New, Neutron-Rich Isotopes of Bismuth, Lead and Thallium by means of a Pulsed Release Element Selective Method

    CERN Multimedia

    Mills, A; Kugler, E; Van duppen, P L E; Lettry, J

    2002-01-01

    % IS354 \\\\ \\\\ It is proposed to produce, identify and investigate at ISOLDE new, neutron-rich isotopes of bismuth, lead and thallium at the mass numbers A=215 to A=218. A recently tested operation mode of the PS Booster-ISOLDE complex, taking an advantage of the unique pulsed proton beam structure, will be used together with a ThC target in order to increase the selectivity. The decay properties of new nuclides will be studied by means of $\\beta$-, $\\gamma$- and X- ray spectroscopy methods. The expected information on the $\\beta$-half-lives and excited states will be used for testing and developing the nuclear structure models ``south-east'' of $^{208}$Pb, and will provide input data for the description of the r-process path at very heavy nuclei. The proposed study of the yields and the decay properties of those heavy nuclei produced in the spallation of $^{232}$Th by a 1~GeV proton beam contributes also the data necessary for the simulations of a hybrid accelerator-reactor system.

  20. Mesozoic vein-type Pb-Zn mineralization in the Pyrenees: Lead isotopic and fluid inclusion evidence from the Les Argentières and Lacore deposits

    Science.gov (United States)

    Munoz, Marguerite; Baron, Sandrine; Boucher, Adrien; Béziat, Didier; Salvi, Stefano

    2016-03-01

    The Axial Zone of the Pyrenees contains numerous sedimentary-exhalative Pb-Zn deposits formed during the Early Palaeozoic, which have been the subject of several studies. In addition to these, base-metal vein-type mineralizations are also exposed within the Axial Zone metasediments. These deposits, however, have not been investigated in depth and the timing and geodynamic context of their formation has not been specifically addressed. The vein-type Pb-Zn deposits of Les Argentières and Lacore are located in Devonian terranes of the eastern Pyrenees, south of the Mesozoic Aulus basin. They are interpreted as having been emplaced under an extensional setting. They are characterized by silver-rich tetrahedrite that occurs with Pb-Zn sulphides deposited by low-temperature NaCl-CaCl2 brines. Lead isotopic 208Pb/204Pb and 206Pb/204Pb ratios acquired on galena show more radiogenic values compared to those from the Palaeozoic sedimentary-exhalative mineralization, thus indicating younger ages. According to the model ages, the formation of the two deposits may be narrowed down to middle Late Triassic and Late Jurassic periods, respectively, which allows us to argue in favour of the role of pre-Alpine rifting phases in hydrothermal fluids circulation and mineralization deposition in a vein system bounding the Mesozoic Aulus basin.

  1. Influences upon the lead isotopic composition of organic and mineral horizons in soil profiles from the National Soil Inventory of Scotland (2007–09)

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, John G., E-mail: J.G.Farmer@ed.ac.uk [School of GeoSciences, The University of Edinburgh, Crew Building, Alexander Crum Brown Road, Edinburgh, EH9 3FF Scotland (United Kingdom); Graham, Margaret C. [School of GeoSciences, The University of Edinburgh, Crew Building, Alexander Crum Brown Road, Edinburgh, EH9 3FF Scotland (United Kingdom); Eades, Lorna J. [School of Chemistry, The University of Edinburgh, Joseph Black Building, David Brewster Road, Edinburgh, EH9 3FJ Scotland (United Kingdom); Lilly, Allan; Bacon, Jeffrey R. [James Hutton Institute, Craigiebuckler, Aberdeen, AB15 8QH Scotland (United Kingdom)

    2016-02-15

    Some 644 individual soil horizons from 169 sites in Scotland were analyzed for Pb concentration and isotopic composition. There were three scenarios: (i) 36 sites where both top and bottom (i.e. lowest sampled) soil horizons were classified as organic in nature, (ii) 67 with an organic top but mineral bottom soil horizon, and (iii) 66 where both top and bottom soil horizons were mineral. Lead concentrations were greater in the top horizon relative to the bottom horizon in all but a few cases. The top horizon {sup 206}Pb/{sup 207}Pb ratio was lesser (outside analytical error) than the corresponding bottom horizon {sup 206}Pb/{sup 207}Pb ratio at (i) 64%, (ii) 94% and (iii) 73% of sites, and greater at only (i) 8%, (ii) 3% and (iii) 8% of sites. A plot of {sup 208}Pb/{sup 207}Pb vs. {sup 208}Pb/{sup 206}Pb ratios showed that the Pb in organic top (i, ii) and bottom (i) horizons was consistent with atmospherically deposited Pb of anthropogenic origin. The {sup 206}Pb/{sup 207}Pb ratio of the organic top horizon in (ii) was unrelated to the {sup 206}Pb/{sup 207}Pb ratio of the mineral bottom horizon as demonstrated by the geographical variation in the negative shift in the ratio, a result of differences in the mineral horizon values arising from the greater influence of radiogenic Pb in the north. In (iii), the lesser values of the {sup 206}Pb/{sup 207}Pb ratio for the mineral top horizon relative to the mineral bottom horizon were consistent with the presence of anthropogenic Pb, in addition to indigenous Pb, in the former. Mean anthropogenic Pb inventories of 1.5 and 4.5 g m{sup −2} were obtained for the northern and southern halves of Scotland, respectively, consistent with long-range atmospheric transport of anthropogenic Pb (mean {sup 206}Pb/{sup 207}Pb ratio ~ 1.16). For cultivated agricultural soils (Ap), this corresponded to about half of the total Pb inventory in the top 30 cm of the soil column. - Highlights: • Pb isotope ratios were determined for 644

  2. Bioautography with TLC-MS/NMR for Rapid Discovery of Anti-tuberculosis Lead Compounds from Natural Sources.

    Science.gov (United States)

    Grzelak, Edyta M; Hwang, Changhwa; Cai, Geping; Nam, Joo-Won; Choules, Mary P; Gao, Wei; Lankin, David C; McAlpine, James B; Mulugeta, Surafel G; Napolitano, José G; Suh, Joo-Won; Yang, Seung Hwan; Cheng, Jinhua; Lee, Hanki; Kim, Jin-Yong; Cho, Sang-Hyun; Pauli, Guido F; Franzblau, Scott G; Jaki, Birgit U

    2016-04-08

    While natural products constitute an established source of lead compounds, the classical iterative bioassay-guided isolation process is both time- and labor-intensive and prone to failing to identify active minor constituents. (HP)TLC-bioautography-MS/NMR, which combines cutting-edge microbiological, chromatographic, and spectrometric technologies, was developed to accelerate anti-tuberculosis (TB) drug discovery from natural sources by acquiring structural information at a very early stage of the isolation process. Using the avirulent, bioluminescent Mtb strain mc(2)7000 luxABCDE, three variations of bioautography were evaluated and optimized for sensitivity in detecting anti-TB agents, including established clinical agents and new leads with novel mechanisms of action. Several exemplary applications of this approach to microbial extracts demonstrate its potential as a routine method in anti-TB drug discovery from natural sources.

  3. Using Uranium-series isotopes to understand processes of rapid soil formation in tropical volcanic settings: an example from Basse-Terre, French Guadeloupe

    Science.gov (United States)

    Ma, Lin

    2015-04-01

    Lin Ma1, Yvette Pereyra1, Peter B Sak2, Jerome Gaillardet3, Heather L Buss4 and Susan L Brantley5, (1) University of Texas at El Paso, El Paso, TX, United States, (2) Dickinson College, Carlisle, PA, United States, (3) Institute de Physique d Globe Paris, Paris, France, (4) University of Bristol, Bristol, United Kingdom, (5) Pennsylvania State University Main Campus, University Park, PA, United States Uranium-series isotopes fractionate during chemical weathering and their activity ratios can be used to determine timescales and rates of soil formation. Such soil formation rates provide important information to understand processes related to rapid soil formation in tropical volcanic settings, especially with respect to their fertility and erosion. Recent studies also highlighted the use of U-series isotopes to trace and quantify atmospheric inputs to surface soils. Such a process is particularly important in providing mineral nutrients to ecosystems in highly depleted soil systems such as the tropical soils. Here, we report U-series isotope compositions in thick soil profiles (>10 m) developed on andesitic pyroclastic flows in Basse-Terre Island of French Guadeloupe. Field observations have shown heterogeneity in color and texture in these thick profiles. However, major element chemistry and mineralogy show some general depth trends. The main minerals present throughout the soil profile are halloysite and gibbsite. Chemically immobile elements such as Al, Fe, and Ti show a depletion profile relative to Th while elements such as K, Mn, and Si show a partial depletion profile at depth. Mobile elements such as Ca, Mg, and Sr have undergone intensive weathering at depths, and an addition profile near the surface, most likely related to atmospheric inputs. (238U/232Th) activity ratios in one soil profile from the Brad David watershed in this study ranged from 0.374 to 1.696, while the (230Th/232Th) ratios ranged from 0.367 to 1.701. A decrease of (238U/232Th) in the

  4. Centrality and rapidity dependence of inclusive jet production in sNN=5.02 TeV proton–lead collisions with the ATLAS detector

    Directory of Open Access Journals (Sweden)

    G. Aad

    2015-09-01

    Full Text Available Measurements of the centrality and rapidity dependence of inclusive jet production in sNN=5.02 TeV proton–lead (p+Pb collisions and the jet cross-section in s=2.76 TeV proton–proton collisions are presented. These quantities are measured in datasets corresponding to an integrated luminosity of 27.8 nb−1 and 4.0 pb−1, respectively, recorded with the ATLAS detector at the Large Hadron Collider in 2013. The p+Pb collision centrality was characterised using the total transverse energy measured in the pseudorapidity interval −4.9<η<−3.2 in the direction of the lead beam. Results are presented for the double-differential per-collision yields as a function of jet rapidity and transverse momentum (pT for minimum-bias and centrality-selected p+Pb collisions, and are compared to the jet rate from the geometric expectation. The total jet yield in minimum-bias events is slightly enhanced above the expectation in a pT-dependent manner but is consistent with the expectation within uncertainties. The ratios of jet spectra from different centrality selections show a strong modification of jet production at all pT at forward rapidities and for large pT at mid-rapidity, which manifests as a suppression of the jet yield in central events and an enhancement in peripheral events. These effects imply that the factorisation between hard and soft processes is violated at an unexpected level in proton–nucleus collisions. Furthermore, the modifications at forward rapidities are found to be a function of the total jet energy only, implying that the violations may have a simple dependence on the hard parton–parton kinematics.

  5. Lead isotopic exploration intersecting mineralization zones for the depth forecast of concealed deposits——A case from Longbohe Cu deposit,Jinping, Yunnan Province,China

    Institute of Scientific and Technical Information of China (English)

    常向阳; 朱炳泉; 邹日

    2000-01-01

    Pb isotopic geochemical exploration intersecting mineralization zones have been well developed in the light of the eigenvalues V1 and V2 of three-dimensional topological projection of Pb isotopic data. The newly developed theoretical model forecasting concealed deposits has been verified in the evaluation of Longbohe copper deposit in Jinping, Yunnan Province, which is consistent with the observed law of depth variation for Pb isotopes. The forecasting results show that the depth of buried major orebody should occur at about -50 to -400 m and deeper within the eastern and western mineralization belts of Longbohe copper deposit.

  6. Physical exercise leads to rapid adaptations in hippocampal vasculature: temporal dynamics and relationship to cell proliferation and neurogenesis.

    Science.gov (United States)

    Van der Borght, Karin; Kóbor-Nyakas, Dóra E; Klauke, Karin; Eggen, Bart J L; Nyakas, Csaba; Van der Zee, Eddy A; Meerlo, Peter

    2009-10-01

    Increased levels of angiogenesis and neurogenesis possibly mediate the beneficial effects of physical activity on hippocampal plasticity. This study was designed to investigate the temporal dynamics of exercise-induced changes in hippocampal angiogenesis and cell proliferation. Mice were housed with a running wheel for 1, 3, or 10 days. Analysis of glucose transporter Glut1-positive vessel density showed a significant increase after 3 days of wheel running. Cell proliferation in the dentate gyrus showed a trend towards an increase after 3 days of running and was significantly elevated after 10 days of physical exercise. Ten days of wheel running resulted in a near-significant increase in the number of immature neurons, as determined by a doublecortin (DCX) staining. In the second part of the study, the persistence of the exercise-induced changes in angiogenesis and cell proliferation was determined. The running wheel was removed from the cage after 10 days of physical activity. Glut-1 positive vessel density and hippocampal cell proliferation were determined 1 and 6 days after removal of the wheel. Both parameters had returned to baseline 24 h after cessation of physical activity. The near-significant increase in the number of DCX-positive immature neurons persisted for at least 6 days, indicating that new neurons formed during the period of increased physical activity had survived. Together these experiments show that the hippocampus displays a remarkable angiogenic and neurogenic plasticity and rapidly responds to changes in physical activity.

  7. Chirally Pure Prodrugs and Their Converting Enzymes Lead to High Supersaturation and Rapid Transcellular Permeation of Benzodiazepines.

    Science.gov (United States)

    Kapoor, Mamta; Cheryala, Narsihmulu; Rautiola, Davin; Georg, Gunda I; Cloyd, James C; Siegel, Ronald A

    2016-08-01

    Water-soluble prodrugs can be rapidly converted by enzymes to hydrophobic drugs, whose aqueous thermodynamic solubilities are low, but are maintained in aqueous solution at supersaturated concentrations due to slow precipitation kinetics. Recently, we investigated avizafone (AVF) in combination with Aspergillus oryzae protease as a prodrug/enzyme system intended to produce supersaturated diazepam (DZP). Several fold enhancement of permeation of supersaturated DZP across Madin-Darby canine kidney II-wild type (MDCKII-wt) monolayers was observed, compared to saturated DZP solutions. However, prodrug conversion was incomplete, putatively due to partial racemization of AVF and stereoselectivity of A oryzae protease. Here we report synthesis of chirally pure AVF, and demonstrate complete conversion to supersaturated DZP followed by complete DZP permeation at enhanced rates across MDCKII-wt cell monolayers. We also synthesized, for the first time, a chirally pure prodrug of midazolam (MDZ-pro) and carried out the same sequence of studies. A oryzae protease was identified as a benign and efficient activating enzyme for MDZ-pro. The MDZ-pro/A oryzae protease system showed greater than 25-fold increase in absorption rate of MDZ across MDCKII-wt monolayers, compared to saturated MDZ. Such chirally pure prodrug/enzyme systems are promising candidates for efficient intranasal delivery of benzodiazepine drugs used in the treatment of seizure emergencies. Copyright © 2016 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

  8. Does Rapid and Sustained Economic Growth Lead to Convergence in Health Resources: The Case of China From 1980 to 2010.

    Science.gov (United States)

    Liang, Di; Zhang, Donglan; Huang, Jiayan; Schweitzer, Stuart

    2016-01-01

    China's rapid and sustained economic growth offers an opportunity to ask whether the advantages of growth diffuse throughout an economy, or remain localized in areas where the growth has been the greatest. A critical policy area in China has been the health system, and health inequality has become an issue that has led the government to broaden national health insurance programs. This study investigates whether health system resources and performance have converged over the past 30 years across China's 31 provinces. To examine geographic variation of health system resources and performance at the provincial level, we measure the degree of sigma convergence and beta convergence in indicators of health system resources (structure), health services utilization (process), and outcome. All data are from officially published sources: the China Health Statistics Year Book and the China Statistics Year Book. Sigma convergence is found for resource indicators, whereas it is not observed for either process or outcome indicators, indicating that disparities only narrowed in health system resources. Beta convergence is found in most indicators, except for 2 procedure indicators, reflecting that provinces with poorer resources were catching up. Convergence found in this study probably reflects the mixed outcome of government input, and market forces. Thus, left alone, the equitable distribution of health care resources may not occur naturally during a period of economic growth. Governmental and societal efforts are needed to reduce geographic health variation and promote health equity.

  9. Lead and sulfur isotopes of Guarn Halfaya and Bou Grine deposits associated to salt dome cap rocks (Diapirs zone, Northern Tunisia): sources of metals and genetic model

    Science.gov (United States)

    Jemmali, N.; Souissi, F.; Carranza, E. J. M.; Vennemann, T. W.

    2012-04-01

    The Pb-Zn ores districts at Guarn Halfaya and Bou Grine are hosted mainly by the dolostones in the contact breccias between Triassic and Upper Cretaceous and by Upper Cretaceous limestones. The mineralization occurs as lenticular, impregnations, substitutions, replacements, stratiform, vein, dissemination, and stockwork. A complex polymetallic sulfide assemblage typifies the main ore stage, dominated by sphalerite and galena, pyrite with minor chalcopyrite, arsenopyrite, and sulfosalt (grey copper). Limestone, barite and celestite dominate the gangue, with lesser calcite. Barite and celestite intergrown with main ore-stage sulfides of Oum Edeboua has δ34S values of 12.7 to 15.0 ‰, consistent with the derivation of sulfate from Triassic evaporites form the study area (12.8reduction (TSR) of Triassic sulfates at depth. However, the presence of bacterial relics suggests involvement of bacterially-mediated sulfate reduction (BSR). The lead isotope composition is homogeneous with 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratio ranging between from 18.723 to 18.783, 15.667 to 15.685, and 38.806 to 38.889, respectively, and plot between the upper crust and orogene curves of Zartman and Doe (1981) which imply involvement of a well-mixed multi-source reservoir of Pb at depth. The syn-diagenetic mineralization in the Bahloul Formation and the calculate of model age suggest a Late Cretaceous age, correspond to a NE-SW to ENE-WSS regional extensional tectonic events, which likely favored migration of mineralizing fluids and eventual deposition at Guarn Halfaya and Bou Grine.

  10. Evaluation of lead isotope compositions of NIST NBS 981 measured by thermal ionization mass spectrometer and multiple-collector inductively coupled plasma mass spectrometer

    Directory of Open Access Journals (Sweden)

    Honglin Yuan

    2016-09-01

    Full Text Available Because Pb isotopes can be used for tracing, they are widely used in many disciplines. The detection and analysis of Pb isotopes of bulk samples are usually conducted using thermal ionization mass spectrometer (TIMS and multiple-collector inductively coupled plasma mass spectrometer (MC-ICP-MS, both of which need external reference materials with known isotopic compositions to correct for the mass discrimination effect produced during analysis. NIST NBS 981 is the most widely used reference material for Pb isotope analysis; however, the isotopic compositions reported by various analytical laboratories, especially those using TIMS, vary from each other. In this study, we statistically evaluated 229 reported TIMS analysis values collected by GeoReM in the last 30 years, 176 reported MC-ICP-MS analysis values, and 938 MC-ICP-MS analysis results from our laboratory in the last five years. After careful investigation, only 40 TIMS results were found to have double or triple spikes. The ratios of the overall weighted averages, 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb, obtained from 40 spiked TIMS reports and 1114 MC-ICP-MS results of NIST NBS 981 isotopes were 16.9406 ± 0.0003 (2s, 15.4957 ± 0.0002 (2s, and 36.7184 ± 0.0007 (2s, respectively.

  11. Rapid determination of lead and cadmium in sewage sludge samples using electrothermal atomic absorption spectrometry with slurry sample introduction

    Energy Technology Data Exchange (ETDEWEB)

    Lopez-Garcia, I.; Vinas, P.; Arroyo-Cortez, J.; Hernandez-Cordoba, M. [Dept. of Analytical Chem., Univ. of Murcia (Spain)

    2000-08-01

    Lead and cadmium concentrations in sewage sludge samples are determined by suspending the ground samples in a solution containing 10% (v/v) concentrated hydrofluoric acid, 1% (v/v) concentrated nitric acid, 0.5% (m/v) dihydrogen ammonium phosphate and 0.1% (m/v) sodium hexametaphosphate. Aliquots of 20 {mu}L of these suspensions (4 mg/mL) are diluted to 1000 {mu}L with the same solution and then injected into the electrothermal atomizer. The drying stage is performed by programming a 400 C temperature, a ramp time of 20 s and a hold time of 15 s on the power supply of the atomizer. No ashing step is used. Platform atomization is carried out at 1600 and 1800 C for Pb and Cd, respectively. Calibration is performed using aqueous standards in the 5-75 and 0.2- 5 {mu}g/L Pb and Cd ranges, respectively. Results obtained for three certified reference materials and four samples demonstrate the reliability of the procedures described. (orig.)

  12. FRET energy transfer via Pdots improves the efficiency of photodynamic therapy and leads to rapid cell death.

    Science.gov (United States)

    Haupt, Sara; Lazar, Itay; Weitman, Hana; Shav-Tal, Yaron; Ehrenberg, Benjamin

    2016-11-01

    Photodynamic therapy (PDT) is well established as a clinical treatment modality for various diseases, including cancer and especially for the treatment of superficial tumors. However, one of the disadvantages of the photoactivatable molecules is their low absorbance in the optical window for photosensitizer excitation. The use of nanoparticles in photodynamic therapy can address this deficiency and improve treatment efficiency. Pdots are nano-sized particles, composed of conjugated chromophoric polymers. By mixing them with PEGylated phospholipids they can become soluble and stable colloids. They exhibit a broad absorption band with a strong and narrow emission band. In this study, we examined two types of Pdots (MEH-PPV and CN-PPV) with two different lengths of the PEGylated lipids coating, 350 and 2000. When a photosensitizer, such as mTHPC, comes in close contact with the amphiphilic coating of the Pdots, a very efficient fluorescence resonance energy transfer (FRET) occurs between the donor, the Pdots and the acceptor, the sensitizer. This process, together with the significant uptake of the Pdots-sensitizer pair by MCF-7 cancerous cells causes irreversible damage to the cells. This damage is greater when the Pdots are comprised from the CN-PPV polymer and coated with the PEG2000-PE lipid. Altogether, we demonstrate that implementing FRET energy transfer in the PDT protocol leads to quicker and more aggressive cell death, thus improving the efficacy of the photodynamic therapy.

  13. Rapid Proteasomal Degradation of Mutant Proteins Is the Primary Mechanism Leading to Tumorigenesis in Patients With Missense AIP Mutations

    Science.gov (United States)

    Hernández-Ramírez, Laura C.; Martucci, Federico; Morgan, Rhodri M. L.; Trivellin, Giampaolo; Tilley, Daniel; Ramos-Guajardo, Nancy; Iacovazzo, Donato; D'Acquisto, Fulvio; Prodromou, Chrisostomos

    2016-01-01

    Context: The pathogenic effect of mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene (AIPmuts) in pituitary adenomas is incompletely understood. We have identified the primary mechanism of loss of function for missense AIPmuts. Objective: This study sought to analyze the mechanism/speed of protein turnover of wild-type and missense AIP variants, correlating protein half-life with clinical parameters. Design and Setting: Half-life and protein–protein interaction experiments and cross-sectional analysis of AIPmut positive patients' data were performed in a clinical academic research institution. Patients: Data were obtained from our cohort of pituitary adenoma patients and literature-reported cases. Interventions: Protein turnover of endogenous AIP in two cell lines and fifteen AIP variants overexpressed in HEK293 cells was analyzed via cycloheximide chase and proteasome inhibition. Glutathione-S-transferase pull-down and quantitative mass spectrometry identified proteins involved in AIP degradation; results were confirmed by coimmunoprecipitation and gene knockdown. Relevant clinical data was collected. Main Outcome Measures: Half-life of wild-type and mutant AIP proteins and its correlation with clinical parameters. Results: Endogenous AIP half-life was similar in HEK293 and lymphoblastoid cells (43.5 and 32.7 h). AIP variants were divided into stable proteins (median, 77.7 h; interquartile range [IQR], 60.7–92.9 h), and those with short (median, 27 h; IQR, 21.6–28.7 h) or very short (median, 7.7 h; IQR, 5.6–10.5 h) half-life; proteasomal inhibition rescued the rapid degradation of mutant proteins. The experimental half-life significantly correlated with age at diagnosis of acromegaly/gigantism (r = 0.411; P = .002). The FBXO3-containing SKP1–CUL1–F-box protein complex was identified as the E3 ubiquitin-ligase recognizing AIP. Conclusions: AIP is a stable protein, driven to ubiquitination by the SKP1–CUL1–F-box protein complex

  14. A rapid method for simultaneous determination of arsenic, cadmium and lead in drinking water by inductively coupled plasma mass spectrometry

    Directory of Open Access Journals (Sweden)

    Joshua Rey P. Torres

    Full Text Available The raw water source of drinking water in most areas in the Philippines is typically river water and in some cases groundwater. These sources are prone to elevated levels of metals and metalloids that may cause exposure of the general population when the treatment of the water is inadequate. This work presents a simple method based on EPA Method 200.8 for the determination of total concentrations of arsenic (As, cadmium (Cd and lead (Pb in drinking water using inductively coupled plasma-mass spectrometry (ICP-MS as the element-selective detector. This was applied in the determination of these elements in the water supply in Metro Manila, Philippines. The method detection limits were 0.095 μg L-1, 0.043 μg L-1, and 0.114 μg L-1 for total As, Cd and Pb, respectively.The method was validated using National Institute of Standards and Technology (NIST 1643e certified reference material for trace elements in water and determined values were 60.4 ± 0.5 μg L-1, 6.7 ± 0.1 μg L-1, and 19.6 ± 0.5 μg L-1 for As, Cd and Pb, respectively. These determined values were in good agreement with the certified values in the reference material. Analysis of actual drinking water samples showed that most samples did not exceed the limit of the Philippine drinking water standard for the elements.

  15. Lead and strontium isotopic evidence for crustal interaction and compositional zonation in the source regions of Pleistocene basaltic and rhyolitic magmas of the Coso volcanic field, California

    Science.gov (United States)

    Bacon, C.R.; Kurasawa, H.; Delevaux, M.H.; Kistler, R.W.; Doe, B.R.

    1984-01-01

    The isotopic compositions of Pb and Sr in Pleistocene basalt, high-silica rhyolite, and andesitic inclusions in rhyolite of the Coso volcanic field indicate that these rocks were derived from different levels of compositionally zoned magmatic systems. The 2 earliest rhyolites probably were tapped from short-lived silicic reservoirs, in contrast to the other 36 rhyolite domes and lava flows which the isotopic data suggest may have been leaked from the top of a single, long-lived magmatic system. Most Coso basalts show isotopic, geochemical, and mineralogic evidence of interaction with crustal rocks, but one analyzed flow has isotopic ratios that may represent mantle values (87Sr/86Sr=0.7036,206Pb/204Pb=19.05,207Pb/204Pb=15.62,208Pb/204Pb= 38.63). The (initial) isotopic composition of typical rhyolite (87Sr/86Sr=0.7053,206Pb/204Pb=19.29,207Pb/204Pb= 15.68,208Pb/204Pb=39.00) is representative of the middle or upper crust. Andesitic inclusions in the rhyolites are evidently samples of hybrid magmas from the silicic/mafic interface in vertically zoned magma reservoirs. Silicic end-member compositions inferred for these mixed magmas, however, are not those of erupted rhyolite but reflect the zonation within the silicic part of the magma reservoir. The compositional contrast at the interface between mafic and silicic parts of these systems apparently was greater for the earlier, smaller reservoirs. ?? 1984 Springer-Verlag.

  16. Centrality and rapidity dependence of inclusive jet production in $\\sqrt{s_\\mathrm{NN}}$ = 5.02 TeV proton--lead collisions with the ATLAS detector

    CERN Document Server

    Aad, Georges; Abdallah, Jalal; Abdel Khalek, Samah; Abdinov, Ovsat; Aben, Rosemarie; Abi, Babak; Abolins, Maris; AbouZeid, Ossama; Abramowicz, Halina; Abreu, Henso; Abreu, Ricardo; Abulaiti, Yiming; Acharya, Bobby Samir; Adamczyk, Leszek; Adams, David; Adelman, Jahred; Adomeit, Stefanie; Adye, Tim; Agatonovic-Jovin, Tatjana; Aguilar-Saavedra, Juan Antonio; Agustoni, Marco; Ahlen, Steven; Ahmadov, Faig; Aielli, Giulio; Akerstedt, Henrik; Åkesson, Torsten Paul Ake; Akimoto, Ginga; Akimov, Andrei; Alberghi, Gian Luigi; Albert, Justin; Albrand, Solveig; Alconada Verzini, Maria Josefina; Aleksa, Martin; Aleksandrov, Igor; Alexa, Calin; Alexander, Gideon; Alexandre, Gauthier; Alexopoulos, Theodoros; Alhroob, Muhammad; Alimonti, Gianluca; Alio, Lion; Alison, John; Allbrooke, Benedict; Allison, Lee John; Allport, Phillip; Almond, John; Aloisio, Alberto; Alonso, Alejandro; Alonso, Francisco; Alpigiani, Cristiano; Altheimer, Andrew David; Alvarez Gonzalez, Barbara; Alviggi, Mariagrazia; Amako, Katsuya; Amaral Coutinho, Yara; Amelung, Christoph; Amidei, Dante; Amor Dos Santos, Susana Patricia; Amorim, Antonio; Amoroso, Simone; Amram, Nir; Amundsen, Glenn; Anastopoulos, Christos; Ancu, Lucian Stefan; Andari, Nansi; Andeen, Timothy; Anders, Christoph Falk; Anders, Gabriel; Anderson, Kelby; Andreazza, Attilio; Andrei, George Victor; Anduaga, Xabier; Angelidakis, Stylianos; Angelozzi, Ivan; Anger, Philipp; Angerami, Aaron; Anghinolfi, Francis; Anisenkov, Alexey; Anjos, Nuno; Annovi, Alberto; Antonaki, Ariadni; Antonelli, Mario; Antonov, Alexey; Antos, Jaroslav; Anulli, Fabio; Aoki, Masato; Aperio Bella, Ludovica; Apolle, Rudi; Arabidze, Giorgi; Aracena, Ignacio; Arai, Yasuo; Araque, Juan Pedro; Arce, Ayana; Arguin, Jean-Francois; Argyropoulos, Spyridon; Arik, Metin; Armbruster, Aaron James; Arnaez, Olivier; Arnal, Vanessa; Arnold, Hannah; Arratia, Miguel; Arslan, Ozan; Artamonov, Andrei; Artoni, Giacomo; Asai, Shoji; Asbah, Nedaa; Ashkenazi, Adi; Åsman, Barbro; Asquith, Lily; Assamagan, Ketevi; Astalos, Robert; Atkinson, Markus; Atlay, Naim Bora; Auerbach, Benjamin; Augsten, Kamil; Aurousseau, Mathieu; Avolio, Giuseppe; Azuelos, Georges; Azuma, Yuya; Baak, Max; Baas, Alessandra; Bacci, Cesare; Bachacou, Henri; Bachas, Konstantinos; Backes, Moritz; Backhaus, Malte; Backus Mayes, John; Badescu, Elisabeta; Bagiacchi, Paolo; Bagnaia, Paolo; Bai, Yu; Bain, Travis; Baines, John; Baker, Oliver Keith; Balek, Petr; Balli, Fabrice; Banas, Elzbieta; Banerjee, Swagato; Bannoura, Arwa A E; Bansal, Vikas; Bansil, Hardeep Singh; Barak, Liron; Baranov, Sergei; Barberio, Elisabetta Luigia; Barberis, Dario; Barbero, Marlon; Barillari, Teresa; Barisonzi, Marcello; Barklow, Timothy; Barlow, Nick; Barnett, Bruce; Barnett, Michael; Barnovska, Zuzana; Baroncelli, Antonio; Barone, Gaetano; Barr, Alan; Barreiro, Fernando; Barreiro Guimarães da Costa, João; Bartoldus, Rainer; Barton, Adam Edward; Bartos, Pavol; Bartsch, Valeria; Bassalat, Ahmed; Basye, Austin; Bates, Richard; Batley, Richard; Battaglia, Marco; Battistin, Michele; Bauer, Florian; Bawa, Harinder Singh; Beattie, Michael David; Beau, Tristan; Beauchemin, Pierre-Hugues; Beccherle, Roberto; Bechtle, Philip; Beck, Hans Peter; Becker, Anne Kathrin; Becker, Sebastian; Beckingham, Matthew; Becot, Cyril; Beddall, Andrew; Beddall, Ayda; Bedikian, Sourpouhi; Bednyakov, Vadim; Bee, Christopher; Beemster, Lars; Beermann, Thomas; Begel, Michael; Behr, Katharina; Belanger-Champagne, Camille; Bell, Paul; Bell, William; Bella, Gideon; Bellagamba, Lorenzo; Bellerive, Alain; Bellomo, Massimiliano; Belotskiy, Konstantin; Beltramello, Olga; Benary, Odette; Benchekroun, Driss; Bendtz, Katarina; Benekos, Nektarios; Benhammou, Yan; Benhar Noccioli, Eleonora; Benitez Garcia, Jorge-Armando; Benjamin, Douglas; Bensinger, James; Benslama, Kamal; Bentvelsen, Stan; Berge, David; Bergeaas Kuutmann, Elin; Berger, Nicolas; Berghaus, Frank; Beringer, Jürg; Bernard, Clare; Bernat, Pauline; Bernius, Catrin; Bernlochner, Florian Urs; Berry, Tracey; Berta, Peter; Bertella, Claudia; Bertoli, Gabriele; Bertolucci, Federico; Bertsche, Carolyn; Bertsche, David; Besana, Maria Ilaria; Besjes, Geert-Jan; Bessidskaia, Olga; Bessner, Martin Florian; Besson, Nathalie; Betancourt, Christopher; Bethke, Siegfried; Bhimji, Wahid; Bianchi, Riccardo-Maria; Bianchini, Louis; Bianco, Michele; Biebel, Otmar; Bieniek, Stephen Paul; Bierwagen, Katharina; Biesiada, Jed; Biglietti, Michela; Bilbao De Mendizabal, Javier; Bilokon, Halina; Bindi, Marcello; Binet, Sebastien; Bingul, Ahmet; Bini, Cesare; Black, Curtis; Black, James

    2015-01-01

    Measurements of the centrality and rapidity dependence of inclusive jet production in $\\sqrt{s_\\mathrm{NN}} = 5.02$ TeV proton--lead ($p$+Pb) collisions and the jet cross-section in $\\sqrt{s} = 2.76$ TeV proton--proton collisions are presented. These quantities are measured in datasets corresponding to an integrated luminosity of 27.8 nb$^{-1}$ and 4.0 pb$^{-1}$, respectively, recorded with the ATLAS detector at the Large Hadron Collider in 2013. The $p$+Pb collision centrality was characterised using the total transverse energy measured in the pseudorapidity interval $-4.9 < \\eta < -3.2$ in the direction of the lead beam. Results are presented for the double-differential per-collision yields as a function of jet rapidity and transverse momentum ($p_\\mathrm{T}$) for minimum-bias and centrality-selected $p$+Pb collisions, and are compared to the jet rate from the geometric expectation. The total jet yield in minimum-bias events is slightly enhanced above the expectation in a $p_\\mathrm{T}$-dependent mann...

  17. Study of dijet events with a large rapidity gap between the two leading jets in pp collisions at $\\sqrt{s}= $ 7 TeV

    CERN Document Server

    Sirunyan, Albert M; CMS Collaboration; Adam, Wolfgang; Asilar, Ece; Bergauer, Thomas; Brandstetter, Johannes; Brondolin, Erica; Dragicevic, Marko; Erö, Janos; Flechl, Martin; Friedl, Markus; Fruehwirth, Rudolf; Ghete, Vasile Mihai; Hartl, Christian; Krammer, Natascha; Hrubec, Josef; Jeitler, Manfred; König, Axel; Krätschmer, Ilse; Liko, Dietrich; Matsushita, Takashi; Mikulec, Ivan; Rabady, Dinyar; Rad, Navid; Rahbaran, Babak; Rohringer, Herbert; Schieck, Jochen; Strauss, Josef; Waltenberger, Wolfgang; Wulz, Claudia-Elisabeth; Dvornikov, Oleg; Makarenko, Vladimir; Mossolov, Vladimir; Suarez Gonzalez, Juan; Zykunov, Vladimir; Shumeiko, Nikolai; Alderweireldt, Sara; De Wolf, Eddi A; Janssen, Xavier; Lauwers, Jasper; Van De Klundert, Merijn; Van Haevermaet, Hans; Van Mechelen, Pierre; Van Remortel, Nick; Van Spilbeeck, Alex; Abu Zeid, Shimaa; Blekman, Freya; D'Hondt, Jorgen; Daci, Nadir; De Bruyn, Isabelle; Deroover, Kevin; Lowette, Steven; Moortgat, Seth; Moreels, Lieselotte; Olbrechts, Annik; Python, Quentin; Skovpen, Kirill; Tavernier, Stefaan; Van Doninck, Walter; Van Mulders, Petra; Van Parijs, Isis; Brun, Hugues; Clerbaux, Barbara; De Lentdecker, Gilles; Delannoy, Hugo; Fasanella, Giuseppe; Favart, Laurent; Goldouzian, Reza; Grebenyuk, Anastasia; Karapostoli, Georgia; Lenzi, Thomas; Léonard, Alexandre; Luetic, Jelena; Maerschalk, Thierry; Marinov, Andrey; Randle-conde, Aidan; Seva, Tomislav; Vander Velde, Catherine; Vanlaer, Pascal; Vannerom, David; Yonamine, Ryo; Zenoni, Florian; Zhang, Fengwangdong; Cimmino, Anna; Cornelis, Tom; Dobur, Didar; Fagot, Alexis; Gul, Muhammad; Khvastunov, Illia; Poyraz, Deniz; Salva Diblen, Sinem; Schöfbeck, Robert; Tytgat, Michael; Van Driessche, Ward; Yazgan, Efe; Zaganidis, Nicolas; Bakhshiansohi, Hamed; Beluffi, Camille; Bondu, Olivier; Brochet, Sébastien; Bruno, Giacomo; Caudron, Adrien; De Visscher, Simon; Delaere, Christophe; Delcourt, Martin; Francois, Brieuc; Giammanco, Andrea; Jafari, Abideh; Komm, Matthias; Krintiras, Georgios; Lemaitre, Vincent; Magitteri, Alessio; Mertens, Alexandre; Musich, Marco; Piotrzkowski, Krzysztof; Quertenmont, Loic; Selvaggi, Michele; Vidal Marono, Miguel; Wertz, Sébastien; Beliy, Nikita; Aldá Júnior, Walter Luiz; Alves, Fábio Lúcio; Alves, Gilvan; Brito, Lucas; Hensel, Carsten; Moraes, Arthur; Pol, Maria Elena; Rebello Teles, Patricia; Belchior Batista Das Chagas, Ewerton; Carvalho, Wagner; Chinellato, Jose; Custódio, Analu; Melo Da Costa, Eliza; Da Silveira, Gustavo Gil; De Jesus Damiao, Dilson; De Oliveira Martins, Carley; Fonseca De Souza, Sandro; Huertas Guativa, Lina Milena; Malbouisson, Helena; Matos Figueiredo, Diego; Mora Herrera, Clemencia; Mundim, Luiz; Nogima, Helio; Prado Da Silva, Wanda Lucia; Santoro, Alberto; Sznajder, Andre; Tonelli Manganote, Edmilson José; Torres Da Silva De Araujo, Felipe; Vilela Pereira, Antonio; Ahuja, Sudha; Bernardes, Cesar Augusto; Dogra, Sunil; Tomei, Thiago; De Moraes Gregores, Eduardo; Mercadante, Pedro G; Moon, Chang-Seong; Novaes, Sergio F; Padula, Sandra; Romero Abad, David; Ruiz Vargas, José Cupertino; Aleksandrov, Aleksandar; Hadjiiska, Roumyana; Iaydjiev, Plamen; Rodozov, Mircho; Stoykova, Stefka; Sultanov, Georgi; Shopova, Mariana; Dimitrov, Anton; Glushkov, Ivan; Litov, Leander; Pavlov, Borislav; Petkov, Peicho; Fang, Wenxing; Ahmad, Muhammad; Bian, Jian-Guo; Chen, Guo-Ming; Chen, He-Sheng; Chen, Mingshui; Chen, Ye; Cheng, Tongguang; Jiang, Chun-Hua; Leggat, Duncan; Liu, Zhenan; Romeo, Francesco; Ruan, Manqi; Shaheen, Sarmad Masood; Spiezia, Aniello; Tao, Junquan; Wang, Chunjie; Wang, Zheng; Zhang, Huaqiao; Zhao, Jingzhou; Ban, Yong; Chen, Geng; Li, Qiang; Liu, Shuai; Mao, Yajun; Qian, Si-Jin; Wang, Dayong; Xu, Zijun; Avila, Carlos; Cabrera, Andrés; Chaparro Sierra, Luisa Fernanda; Florez, Carlos; Gomez, Juan Pablo; González Hernández, Carlos Felipe; Ruiz Alvarez, José David; Sanabria, Juan Carlos; Godinovic, Nikola; Lelas, Damir; Puljak, Ivica; Ribeiro Cipriano, Pedro M; Sculac, Toni; Antunovic, Zeljko; Kovac, Marko; Brigljevic, Vuko; Ferencek, Dinko; Kadija, Kreso; Mesic, Benjamin; Susa, Tatjana; Ather, Mohsan Waseem; Attikis, Alexandros; Mavromanolakis, Georgios; Mousa, Jehad; Nicolaou, Charalambos; Ptochos, Fotios; Razis, Panos A; Rykaczewski, Hans; Finger, Miroslav; Finger Jr, Michael; Carrera Jarrin, Edgar; Elgammal, Sherif; Ellithi Kamel, Ali; Mohamed, Amr; Kadastik, Mario; Perrini, Lucia; Raidal, Martti; Tiko, Andres; Veelken, Christian; Eerola, Paula; Pekkanen, Juska; Voutilainen, Mikko; Härkönen, Jaakko; Jarvinen, Terhi; Karimäki, Veikko; Kinnunen, Ritva; Lampén, Tapio; Lassila-Perini, Kati; Lehti, Sami; Lindén, Tomas; Luukka, Panja-Riina; Tuominiemi, Jorma; Tuovinen, Esa; Wendland, Lauri; Talvitie, Joonas; Tuuva, Tuure; Besancon, Marc; Couderc, Fabrice; Dejardin, Marc; Denegri, Daniel; Fabbro, Bernard; Faure, Jean-Louis; Favaro, Carlotta; Ferri, Federico; Ganjour, Serguei; Ghosh, Saranya; Givernaud, Alain; Gras, Philippe; Hamel de Monchenault, Gautier; Jarry, Patrick; Kucher, Inna; Locci, Elizabeth; Machet, Martina; Malcles, Julie; Rander, John; Rosowsky, André; Titov, Maksym; Abdulsalam, Abdulla; Antropov, Iurii; Baffioni, Stephanie; Beaudette, Florian; Busson, Philippe; Cadamuro, Luca; Chapon, Emilien; Charlot, Claude; Davignon, Olivier; Granier de Cassagnac, Raphael; Jo, Mihee; Lisniak, Stanislav; Miné, Philippe; Nguyen, Matthew; Ochando, Christophe; Ortona, Giacomo; Paganini, Pascal; Pigard, Philipp; Regnard, Simon; Salerno, Roberto; Sirois, Yves; Stahl Leiton, Andre Govinda; Strebler, Thomas; Yilmaz, Yetkin; Zabi, Alexandre; Zghiche, Amina; Agram, Jean-Laurent; Andrea, Jeremy; Bloch, Daniel; Brom, Jean-Marie; Buttignol, Michael; Chabert, Eric Christian; Chanon, Nicolas; Collard, Caroline; Conte, Eric; Coubez, Xavier; Fontaine, Jean-Charles; Gelé, Denis; Goerlach, Ulrich; Le Bihan, Anne-Catherine; Van Hove, Pierre; Gadrat, Sébastien; Beauceron, Stephanie; Bernet, Colin; Boudoul, Gaelle; Carrillo Montoya, Camilo Andres; Chierici, Roberto; Contardo, Didier; Courbon, Benoit; Depasse, Pierre; El Mamouni, Houmani; Fay, Jean; Gascon, Susan; Gouzevitch, Maxime; Grenier, Gérald; Ille, Bernard; Lagarde, Francois; Laktineh, Imad Baptiste; Lethuillier, Morgan; Mirabito, Laurent; Pequegnot, Anne-Laure; Perries, Stephane; Popov, Andrey; Sordini, Viola; Vander Donckt, Muriel; Verdier, Patrice; Viret, Sébastien; Toriashvili, Tengizi; Tsamalaidze, Zviad; Autermann, Christian; Beranek, Sarah; Feld, Lutz; Kiesel, Maximilian Knut; Klein, Katja; Lipinski, Martin; Preuten, Marius; Schomakers, Christian; Schulz, Johannes; Verlage, Tobias; Albert, Andreas; Brodski, Michael; Dietz-Laursonn, Erik; Duchardt, Deborah; Endres, Matthias; Erdmann, Martin; Erdweg, Sören; Esch, Thomas; Fischer, Robert; Güth, Andreas; Hamer, Matthias; Hebbeker, Thomas; Heidemann, Carsten; Hoepfner, Kerstin; Knutzen, Simon; Merschmeyer, Markus; Meyer, Arnd; Millet, Philipp; Mukherjee, Swagata; Olschewski, Mark; Padeken, Klaas; Pook, Tobias; Radziej, Markus; Reithler, Hans; Rieger, Marcel; Scheuch, Florian; Sonnenschein, Lars; Teyssier, Daniel; Thüer, Sebastian; Cherepanov, Vladimir; Flügge, Günter; Kargoll, Bastian; Kress, Thomas; Künsken, Andreas; Lingemann, Joschka; Müller, Thomas; Nehrkorn, Alexander; Nowack, Andreas; Pistone, Claudia; Pooth, Oliver; Stahl, Achim; Aldaya Martin, Maria; Arndt, Till; Asawatangtrakuldee, Chayanit; Beernaert, Kelly; Behnke, Olaf; Behrens, Ulf; Bin Anuar, Afiq Aizuddin; Borras, Kerstin; Campbell, Alan; Connor, Patrick; Contreras-Campana, Christian; Costanza, Francesco; Diez Pardos, Carmen; Dolinska, Ganna; Eckerlin, Guenter; Eckstein, Doris; Eichhorn, Thomas; Eren, Engin; Gallo, Elisabetta; Garay Garcia, Jasone; Geiser, Achim; Gizhko, Andrii; Grados Luyando, Juan Manuel; Grohsjean, Alexander; Gunnellini, Paolo; Harb, Ali; Hauk, Johannes; Hempel, Maria; Jung, Hannes; Kalogeropoulos, Alexis; Karacheban, Olena; Kasemann, Matthias; Keaveney, James; Kleinwort, Claus; Korol, Ievgen; Krücker, Dirk; Lange, Wolfgang; Lelek, Aleksandra; Lenz, Teresa; Leonard, Jessica; Lipka, Katerina; Lobanov, Artur; Lohmann, Wolfgang; Mankel, Rainer; Melzer-Pellmann, Isabell-Alissandra; Meyer, Andreas Bernhard; Mittag, Gregor; Mnich, Joachim; Mussgiller, Andreas; Pitzl, Daniel; Placakyte, Ringaile; Raspereza, Alexei; Roland, Benoit; Sahin, Mehmet Özgür; Saxena, Pooja; Schoerner-Sadenius, Thomas; Spannagel, Simon; Stefaniuk, Nazar; Van Onsem, Gerrit Patrick; Walsh, Roberval; Wissing, Christoph; Blobel, Volker; Centis Vignali, Matteo; Draeger, Arne-Rasmus; Dreyer, Torben; Garutti, Erika; Gonzalez, Daniel; Haller, Johannes; Hoffmann, Malte; Junkes, Alexandra; Klanner, Robert; Kogler, Roman; Kovalchuk, Nataliia; Lapsien, Tobias; Marchesini, Ivan; Marconi, Daniele; Meyer, Mareike; Niedziela, Marek; Nowatschin, Dominik; Pantaleo, Felice; Peiffer, Thomas; Perieanu, Adrian; Scharf, Christian; Schleper, Peter; Schmidt, Alexander; Schumann, Svenja; Schwandt, Joern; Stadie, Hartmut; Steinbrück, Georg; Stober, Fred-Markus Helmut; Stöver, Marc; Tholen, Heiner; Troendle, Daniel; Usai, Emanuele; Vanelderen, Lukas; Vanhoefer, Annika; Vormwald, Benedikt; Akbiyik, Melike; Barth, Christian; Baur, Sebastian; Baus, Colin; Berger, Joram; Butz, Erik; Caspart, René; Chwalek, Thorsten; Colombo, Fabio; De Boer, Wim; Dierlamm, Alexander; Fink, Simon; Freund, Benedikt; Friese, Raphael; Giffels, Manuel; Gilbert, Andrew; Goldenzweig, Pablo; Haitz, Dominik; Hartmann, Frank; Heindl, Stefan Michael; Husemann, Ulrich; Kassel, Florian; Katkov, Igor; Kudella, Simon; Mildner, Hannes; Mozer, Matthias Ulrich; Müller, Thomas; Plagge, Michael; Quast, Gunter; Rabbertz, Klaus; Röcker, Steffen; Roscher, Frank; Schröder, Matthias; Shvetsov, Ivan; Sieber, Georg; Simonis, Hans-Jürgen; Ulrich, Ralf; Wayand, Stefan; Weber, Marc; Weiler, Thomas; Williamson, Shawn; Wöhrmann, Clemens; Wolf, Roger; Anagnostou, Georgios; Daskalakis, Georgios; Geralis, Theodoros; Giakoumopoulou, Viktoria Athina; Kyriakis, Aristotelis; Loukas, Demetrios; Topsis-Giotis, Iasonas; Kesisoglou, Stilianos; Panagiotou, Apostolos; Saoulidou, Niki; Tziaferi, Eirini; Evangelou, Ioannis; Flouris, Giannis; Foudas, Costas; Kokkas, Panagiotis; Loukas, Nikitas; Manthos, Nikolaos; Papadopoulos, Ioannis; Paradas, Evangelos; Filipovic, Nicolas; Pasztor, Gabriella; Bencze, Gyorgy; Hajdu, Csaba; Horvath, Dezso; Sikler, Ferenc; Veszpremi, Viktor; Vesztergombi, Gyorgy; Zsigmond, Anna Julia; Beni, Noemi; Czellar, Sandor; Karancsi, János; Makovec, Alajos; Molnar, Jozsef; Szillasi, Zoltan; Bartók, Márton; Raics, Peter; Trocsanyi, Zoltan Laszlo; Ujvari, Balazs; Komaragiri, Jyothsna Rani; Bahinipati, Seema; Bhowmik, Sandeep; Choudhury, Somnath; Mal, Prolay; Mandal, Koushik; Nayak, Aruna; Sahoo, Deepak Kumar; Sahoo, Niladribihari; Swain, Sanjay Kumar; Bansal, Sunil; Beri, Suman Bala; Bhatnagar, Vipin; Bhawandeep, Bhawandeep; Chawla, Ridhi; Kalsi, Amandeep Kaur; Kaur, Anterpreet; Kaur, Manjit; Kumar, Ramandeep; Kumari, Priyanka; Mehta, Ankita; Mittal, Monika; Singh, Jasbir; Walia, Genius; Kumar, Ashok; Bhardwaj, Ashutosh; Choudhary, Brajesh C; Garg, Rocky Bala; Keshri, Sumit; Malhotra, Shivali; Naimuddin, Md; Ranjan, Kirti; Sharma, Ramkrishna; Sharma, Varun; Bhattacharya, Rajarshi; Bhattacharya, Satyaki; Chatterjee, Kalyanmoy; Dey, Sourav; Dutt, Suneel; Dutta, Suchandra; Ghosh, Shamik; Majumdar, Nayana; Modak, Atanu; Mondal, Kuntal; Mukhopadhyay, Supratik; Nandan, Saswati; Purohit, Arnab; Roy, Ashim; Roy, Debarati; Roy Chowdhury, Suvankar; Sarkar, Subir; Sharan, Manoj; Thakur, Shalini; Behera, Prafulla Kumar; Chudasama, Ruchi; Dutta, Dipanwita; Jha, Vishwajeet; Kumar, Vineet; Mohanty, Ajit Kumar; Netrakanti, Pawan Kumar; Pant, Lalit Mohan; Shukla, Prashant; Topkar, Anita; Aziz, Tariq; Dugad, Shashikant; Kole, Gouranga; Mahakud, Bibhuprasad; Mitra, Soureek; Mohanty, Gagan Bihari; Parida, Bibhuti; Sur, Nairit; Sutar, Bajrang; Banerjee, Sudeshna; Dewanjee, Ram Krishna; Ganguly, Sanmay; Guchait, Monoranjan; Jain, Sandhya; Kumar, Sanjeev; Maity, Manas; Majumder, Gobinda; Mazumdar, Kajari; Sarkar, Tanmay; Wickramage, Nadeesha; Chauhan, Shubhanshu; Dube, Sourabh; Hegde, Vinay; Kapoor, Anshul; Kothekar, Kunal; Pandey, Shubham; Rane, Aditee; Sharma, Seema; Chenarani, Shirin; Eskandari Tadavani, Esmaeel; Etesami, Seyed Mohsen; Khakzad, Mohsen; Mohammadi Najafabadi, Mojtaba; Naseri, Mohsen; Paktinat Mehdiabadi, Saeid; Rezaei Hosseinabadi, Ferdos; Safarzadeh, Batool; Zeinali, Maryam; Felcini, Marta; Grunewald, Martin; Abbrescia, Marcello; Calabria, Cesare; Caputo, Claudio; Colaleo, Anna; Creanza, Donato; Cristella, Leonardo; De Filippis, Nicola; De Palma, Mauro; Fiore, Luigi; Iaselli, Giuseppe; Maggi, Giorgio; Maggi, Marcello; Miniello, Giorgia; My, Salvatore; Nuzzo, Salvatore; Pompili, Alexis; Pugliese, Gabriella; Radogna, Raffaella; Ranieri, Antonio; Selvaggi, Giovanna; Sharma, Archana; Silvestris, Lucia; Venditti, Rosamaria; Verwilligen, Piet; Abbiendi, Giovanni; Battilana, Carlo; Bonacorsi, Daniele; Braibant-Giacomelli, Sylvie; Brigliadori, Luca; Campanini, Renato; Capiluppi, Paolo; Castro, Andrea; Cavallo, Francesca Romana; Chhibra, Simranjit Singh; Codispoti, Giuseppe; Cuffiani, Marco; Dallavalle, Gaetano-Marco; Fabbri, Fabrizio; Fanfani, Alessandra; Fasanella, Daniele; Giacomelli, Paolo; Grandi, Claudio; Guiducci, Luigi; Marcellini, Stefano; Masetti, Gianni; Montanari, Alessandro; Navarria, Francesco; Perrotta, Andrea; Rossi, Antonio; Rovelli, Tiziano; Siroli, Gian Piero; Tosi, Nicolò; Albergo, Sebastiano; Costa, Salvatore; Di Mattia, Alessandro; Giordano, Ferdinando; Potenza, Renato; Tricomi, Alessia; Tuve, Cristina; Barbagli, Giuseppe; Ciulli, Vitaliano; Civinini, Carlo; D'Alessandro, Raffaello; Focardi, Ettore; Lenzi, Piergiulio; Meschini, Marco; Paoletti, Simone; Russo, Lorenzo; Sguazzoni, Giacomo; Strom, Derek; Viliani, Lorenzo; Benussi, Luigi; Bianco, Stefano; Fabbri, Franco; Piccolo, Davide; Primavera, Federica; Calvelli, Valerio; Ferro, Fabrizio; Monge, Maria Roberta; Robutti, Enrico; Tosi, Silvano; Brianza, Luca; Brivio, Francesco; Ciriolo, Vincenzo; Dinardo, Mauro Emanuele; Fiorendi, Sara; Gennai, Simone; Ghezzi, Alessio; Govoni, Pietro; Malberti, Martina; Malvezzi, Sandra; Manzoni, Riccardo Andrea; Menasce, Dario; Moroni, Luigi; Paganoni, Marco; Pedrini, Daniele; Pigazzini, Simone; Ragazzi, Stefano; Tabarelli de Fatis, Tommaso; Buontempo, Salvatore; Cavallo, Nicola; De Nardo, Guglielmo; Di Guida, Salvatore; Fabozzi, Francesco; Fienga, Francesco; Iorio, Alberto Orso Maria; Lista, Luca; Meola, Sabino; Paolucci, Pierluigi; Sciacca, Crisostomo; Thyssen, Filip; Azzi, Patrizia; Bacchetta, Nicola; Benato, Lisa; Bisello, Dario; Boletti, Alessio; Carlin, Roberto; Carvalho Antunes De Oliveira, Alexandra; Checchia, Paolo; Dall'Osso, Martino; De Castro Manzano, Pablo; Dorigo, Tommaso; Dosselli, Umberto; Gasparini, Fabrizio; Gasparini, Ugo; Gozzelino, Andrea; Lacaprara, Stefano; Margoni, Martino; Meneguzzo, Anna Teresa; Pazzini, Jacopo; Pozzobon, Nicola; Ronchese, Paolo; Simonetto, Franco; Torassa, Ezio; Zanetti, Marco; Zotto, Pierluigi; Zumerle, Gianni; Braghieri, Alessandro; Fallavollita, Francesco; Magnani, Alice; Montagna, Paolo; Ratti, Sergio P; Re, Valerio; Riccardi, Cristina; Salvini, Paola; Vai, Ilaria; Vitulo, Paolo; Alunni Solestizi, Luisa; Bilei, Gian Mario; Ciangottini, Diego; Fanò, Livio; Lariccia, Paolo; Leonardi, Roberto; Mantovani, Giancarlo; Mariani, Valentina; Menichelli, Mauro; Saha, Anirban; Santocchia, Attilio; Androsov, Konstantin; Azzurri, Paolo; Bagliesi, Giuseppe; Bernardini, Jacopo; Boccali, Tommaso; Castaldi, Rino; Ciocci, Maria Agnese; Dell'Orso, Roberto; Donato, Silvio; Fedi, Giacomo; Giassi, Alessandro; Grippo, Maria Teresa; Ligabue, Franco; Lomtadze, Teimuraz; Martini, Luca; Messineo, Alberto; Palla, Fabrizio; Rizzi, Andrea; Savoy-Navarro, Aurore; Spagnolo, Paolo; Tenchini, Roberto; Tonelli, Guido; Venturi, Andrea; Verdini, Piero Giorgio; Barone, Luciano; Cavallari, Francesca; Cipriani, Marco; Del Re, Daniele; Diemoz, Marcella; Gelli, Simone; Longo, Egidio; Margaroli, Fabrizio; Marzocchi, Badder; Meridiani, Paolo; Organtini, Giovanni; Paramatti, Riccardo; Preiato, Federico; Rahatlou, Shahram; Rovelli, Chiara; Santanastasio, Francesco; Amapane, Nicola; Arcidiacono, Roberta; Argiro, Stefano; Arneodo, Michele; Bartosik, Nazar; Bellan, Riccardo; Biino, Cristina; Cartiglia, Nicolo; Cenna, Francesca; Costa, Marco; Covarelli, Roberto; Degano, Alessandro; Demaria, Natale; Finco, Linda; Kiani, Bilal; Mariotti, Chiara; Maselli, Silvia; Migliore, Ernesto; Monaco, Vincenzo; Monteil, Ennio; Monteno, Marco; Obertino, Maria Margherita; Pacher, Luca; Pastrone, Nadia; Pelliccioni, Mario; Pinna Angioni, Gian Luca; Ravera, Fabio; Romero, Alessandra; Ruspa, Marta; Sacchi, Roberto; Shchelina, Ksenia; Sola, Valentina; Solano, Ada; Staiano, Amedeo; Traczyk, Piotr; Belforte, Stefano; Casarsa, Massimo; Cossutti, Fabio; Della Ricca, Giuseppe; Zanetti, Anna; Kim, Dong Hee; Kim, Gui Nyun; Kim, Min Suk; Lee, Sangeun; Lee, Seh Wook; Oh, Young Do; Sekmen, Sezen; Son, Dong-Chul; Yang, Yu Chul; Lee, Ari; Kim, Hyunchul; Brochero Cifuentes, Javier Andres; Kim, Tae Jeong; Cho, Sungwoong; Choi, Suyong; Go, Yeonju; Gyun, Dooyeon; Ha, Seungkyu; Hong, Byung-Sik; Jo, Youngkwon; Kim, Yongsun; Lee, Kisoo; Lee, Kyong Sei; Lee, Songkyo; Lim, Jaehoon; Park, Sung Keun; Roh, Youn; Almond, John; Kim, Junho; Lee, Haneol; Oh, Sung Bin; Radburn-Smith, Benjamin Charles; Seo, Seon-hee; Yang, Unki; Yoo, Hwi Dong; Yu, Geum Bong; Choi, Minkyoo; Kim, Hyunyong; Kim, Ji Hyun; Lee, Jason Sang Hun; Park, Inkyu; Ryu, Geonmo; Ryu, Min Sang; Choi, Young-Il; Goh, Junghwan; Hwang, Chanwook; Lee, Jongseok; Yu, Intae; Dudenas, Vytautas; Juodagalvis, Andrius; Vaitkus, Juozas; Ahmed, Ijaz; Ibrahim, Zainol Abidin; Md Ali, Mohd Adli Bin; Mohamad Idris, Faridah; Wan Abdullah, Wan Ahmad Tajuddin; Yusli, Mohd Nizam; Zolkapli, Zukhaimira; Castilla-Valdez, Heriberto; De La Cruz-Burelo, Eduard; Heredia-De La Cruz, Ivan; Hernandez-Almada, Alberto; Lopez-Fernandez, Ricardo; Magaña Villalba, Ricardo; Mejia Guisao, Jhovanny; Sánchez Hernández, Alberto; Carrillo Moreno, Salvador; Oropeza Barrera, Cristina; Vazquez Valencia, Fabiola; Carpinteyro, Severiano; Pedraza, Isabel; Salazar Ibarguen, Humberto Antonio; Uribe Estrada, Cecilia; Morelos Pineda, Antonio; Krofcheck, David; Butler, Philip H; Ahmad, Ashfaq; Ahmad, Muhammad; Hassan, Qamar; Hoorani, Hafeez R; Khan, Wajid Ali; Saddique, Asif; Shah, Mehar Ali; Shoaib, Muhammad; Waqas, Muhammad; Bialkowska, Helena; Bluj, Michal; Boimska, Bozena; Frueboes, Tomasz; Górski, Maciej; Kazana, Malgorzata; Nawrocki, Krzysztof; Romanowska-Rybinska, Katarzyna; Szleper, Michal; Zalewski, Piotr; Bunkowski, Karol; Byszuk, Adrian; Doroba, Krzysztof; Kalinowski, Artur; Konecki, Marcin; Krolikowski, Jan; Misiura, Maciej; Olszewski, Michal; Walczak, Marek; Bargassa, Pedrame; Beirão Da Cruz E Silva, Cristóvão; Calpas, Betty; Di Francesco, Agostino; Faccioli, Pietro; Gallinaro, Michele; Hollar, Jonathan; Leonardo, Nuno; Lloret Iglesias, Lara; Nemallapudi, Mythra Varun; Seixas, Joao; Toldaiev, Oleksii; Vadruccio, Daniele; Varela, Joao; Afanasiev, Serguei; Bunin, Pavel; Gavrilenko, Mikhail; Golutvin, Igor; Gorbunov, Ilya; Kamenev, Alexey; Karjavin, Vladimir; Lanev, Alexander; Malakhov, Alexander; Matveev, Viktor; Palichik, Vladimir; Perelygin, Victor; Shmatov, Sergey; Shulha, Siarhei; Skatchkov, Nikolai; Smirnov, Vitaly; Voytishin, Nikolay; Zarubin, Anatoli; Chtchipounov, Leonid; Golovtsov, Victor; Ivanov, Yury; Kim, Victor; Kuznetsova, Ekaterina; Murzin, Victor; Oreshkin, Vadim; Sulimov, Valentin; Vorobyev, Alexey; Andreev, Yuri; Dermenev, Alexander; Gninenko, Sergei; Golubev, Nikolai; Karneyeu, Anton; Kirsanov, Mikhail; Krasnikov, Nikolai; Pashenkov, Anatoli; Tlisov, Danila; Toropin, Alexander; Epshteyn, Vladimir; Gavrilov, Vladimir; Lychkovskaya, Natalia; Popov, Vladimir; Pozdnyakov, Ivan; Safronov, Grigory; Spiridonov, Alexander; Toms, Maria; Vlasov, Evgueni; Zhokin, Alexander; Aushev, Tagir; Bylinkin, Alexander; Danilov, Mikhail; Polikarpov, Sergey; Tarkovskii, Evgenii; Andreev, Vladimir; Azarkin, Maksim; Dremin, Igor; Kirakosyan, Martin; Leonidov, Andrey; Terkulov, Adel; Baskakov, Alexey; Belyaev, Andrey; Boos, Edouard; Ershov, Alexander; Gribushin, Andrey; Khein, Lev; Klyukhin, Vyacheslav; Kodolova, Olga; Lokhtin, Igor; Lukina, Olga; Miagkov, Igor; Obraztsov, Stepan; Petrushanko, Sergey; Savrin, Viktor; Snigirev, Alexander; Blinov, Vladimir; Skovpen, Yuri; Shtol, Dmitry; Azhgirey, Igor; Bayshev, Igor; Bitioukov, Sergei; Elumakhov, Dmitry; Kachanov, Vassili; Kalinin, Alexey; Konstantinov, Dmitri; Krychkine, Victor; Petrov, Vladimir; Ryutin, Roman; Sobol, Andrei; Troshin, Sergey; Tyurin, Nikolay; Uzunian, Andrey; Volkov, Alexey; Adzic, Petar; Cirkovic, Predrag; Devetak, Damir; Dordevic, Milos; Milosevic, Jovan; Rekovic, Vladimir; Alcaraz Maestre, Juan; Barrio Luna, Mar; Calvo, Enrique; Cerrada, Marcos; Chamizo Llatas, Maria; Colino, Nicanor; De La Cruz, Begona; Delgado Peris, Antonio; Escalante Del Valle, Alberto; Fernandez Bedoya, Cristina; Fernández Ramos, Juan Pablo; Flix, Jose; Fouz, Maria Cruz; Garcia-Abia, Pablo; Gonzalez Lopez, Oscar; Goy Lopez, Silvia; Hernandez, Jose M; Josa, Maria Isabel; Navarro De Martino, Eduardo; Pérez-Calero Yzquierdo, Antonio María; Puerta Pelayo, Jesus; Quintario Olmeda, Adrián; Redondo, Ignacio; Romero, Luciano; Senghi Soares, Mara; Albajar, Carmen; de Trocóniz, Jorge F; Missiroli, Marino; Moran, Dermot; Cuevas, Javier; Fernandez Menendez, Javier; Gonzalez Caballero, Isidro; González Fernández, Juan Rodrigo; Palencia Cortezon, Enrique; Sanchez Cruz, Sergio; Suárez Andrés, Ignacio; Vischia, Pietro; Vizan Garcia, Jesus Manuel; Cabrillo, Iban Jose; Calderon, Alicia; Curras, Esteban; Fernandez, Marcos; Garcia-Ferrero, Juan; Gomez, Gervasio; Lopez Virto, Amparo; Marco, Jesus; Martinez Rivero, Celso; Matorras, Francisco; Piedra Gomez, Jonatan; Rodrigo, Teresa; Ruiz-Jimeno, Alberto; Scodellaro, Luca; Trevisani, Nicolò; Vila, Ivan; Vilar Cortabitarte, Rocio; Abbaneo, Duccio; Auffray, Etiennette; Auzinger, Georg; Baillon, Paul; Ball, Austin; Barney, David; Bloch, Philippe; Bocci, Andrea; Botta, Cristina; Camporesi, Tiziano; Castello, Roberto; Cepeda, Maria; Cerminara, Gianluca; Chen, Yi; D'Enterria, David; Dabrowski, Anne; Daponte, Vincenzo; David Tinoco Mendes, Andre; De Gruttola, Michele; De Roeck, Albert; Di Marco, Emanuele; Dobson, Marc; Dorney, Brian; Du Pree, Tristan; Duggan, Daniel; Dünser, Marc; Dupont, Niels; Elliott-Peisert, Anna; Everaerts, Pieter; Fartoukh, Stephane; Franzoni, Giovanni; Fulcher, Jonathan; Funk, Wolfgang; Gigi, Dominique; Gill, Karl; Girone, Maria; Glege, Frank; Gulhan, Doga; Gundacker, Stefan; Guthoff, Moritz; Harris, Philip; Hegeman, Jeroen; Innocente, Vincenzo; Janot, Patrick; Kieseler, Jan; Kirschenmann, Henning; Knünz, Valentin; Kornmayer, Andreas; Kortelainen, Matti J; Kousouris, Konstantinos; Krammer, Manfred; Lange, Clemens; Lecoq, Paul; Lourenco, Carlos; Lucchini, Marco Toliman; Malgeri, Luca; Mannelli, Marcello; Martelli, Arabella; Meijers, Frans; Merlin, Jeremie Alexandre; Mersi, Stefano; Meschi, Emilio; Milenovic, Predrag; Moortgat, Filip; Morovic, Srecko; Mulders, Martijn; Neugebauer, Hannes; Orfanelli, Styliani; Orsini, Luciano; Pape, Luc; Perez, Emmanuel; Peruzzi, Marco; Petrilli, Achille; Petrucciani, Giovanni; Pfeiffer, Andreas; Pierini, Maurizio; Racz, Attila; Reis, Thomas; Rolandi, Gigi; Rovere, Marco; Sakulin, Hannes; Sauvan, Jean-Baptiste; Schäfer, Christoph; Schwick, Christoph; Seidel, Markus; Sharma, Archana; Silva, Pedro; Sphicas, Paraskevas; Steggemann, Jan; Stoye, Markus; Takahashi, Yuta; Tosi, Mia; Treille, Daniel; Triossi, Andrea; Tsirou, Andromachi; Veckalns, Viesturs; Veres, Gabor Istvan; Verweij, Marta; Wardle, Nicholas; Wöhri, Hermine Katharina; Zagozdzinska, Agnieszka; Zeuner, Wolfram Dietrich; Bertl, Willi; Deiters, Konrad; Erdmann, Wolfram; Horisberger, Roland; Ingram, Quentin; Kaestli, Hans-Christian; Kotlinski, Danek; Langenegger, Urs; Rohe, Tilman; Wiederkehr, Stephan Albert; Bachmair, Felix; Bäni, Lukas; Bianchini, Lorenzo; Casal, Bruno; Dissertori, Günther; Dittmar, Michael; Donegà, Mauro; Grab, Christoph; Heidegger, Constantin; Hits, Dmitry; Hoss, Jan; Kasieczka, Gregor; Lustermann, Werner; Mangano, Boris; Marionneau, Matthieu; Martinez Ruiz del Arbol, Pablo; Masciovecchio, Mario; Meinhard, Maren Tabea; Meister, Daniel; Micheli, Francesco; Musella, Pasquale; Nessi-Tedaldi, Francesca; Pandolfi, Francesco; Pata, Joosep; Pauss, Felicitas; Perrin, Gaël; Perrozzi, Luca; Quittnat, Milena; Rossini, Marco; Schönenberger, Myriam; Starodumov, Andrei; Tavolaro, Vittorio Raoul; Theofilatos, Konstantinos; Wallny, Rainer; Aarrestad, Thea Klaeboe; Amsler, Claude; Caminada, Lea; Canelli, Maria Florencia; De Cosa, Annapaola; Galloni, Camilla; Hinzmann, Andreas; Hreus, Tomas; Kilminster, Benjamin; Ngadiuba, Jennifer; Pinna, Deborah; Rauco, Giorgia; Robmann, Peter; Salerno, Daniel; Seitz, Claudia; Yang, Yong; Zucchetta, Alberto; Candelise, Vieri; Doan, Thi Hien; Jain, Shilpi; Khurana, Raman; Konyushikhin, Maxim; Kuo, Chia-Ming; Lin, Willis; Pozdnyakov, Andrey; Yu, Shin-Shan; Kumar, Arun; Chang, Paoti; Chang, You-Hao; Chao, Yuan; Chen, Kai-Feng; Chen, Po-Hsun; Fiori, Francesco; Hou, George Wei-Shu; Hsiung, Yee; Liu, Yueh-Feng; Lu, Rong-Shyang; Miñano Moya, Mercedes; Paganis, Efstathios; Psallidas, Andreas; Tsai, Jui-fa; Asavapibhop, Burin; Singh, Gurpreet; Srimanobhas, Norraphat; Suwonjandee, Narumon; Adiguzel, Aytul; Cerci, Salim; Damarseckin, Serdal; Demiroglu, Zuhal Seyma; Dozen, Candan; Dumanoglu, Isa; Girgis, Semiray; Gokbulut, Gul; Guler, Yalcin; Hos, Ilknur; Kangal, Evrim Ersin; Kara, Ozgun; Kayis Topaksu, Aysel; Kiminsu, Ugur; Oglakci, Mehmet; Onengut, Gulsen; Ozdemir, Kadri; Sunar Cerci, Deniz; Topakli, Huseyin; Turkcapar, Semra; Zorbakir, Ibrahim Soner; Zorbilmez, Caglar; Bilin, Bugra; Bilmis, Selcuk; Isildak, Bora; Karapinar, Guler; Yalvac, Metin; Zeyrek, Mehmet; Gülmez, Erhan; Kaya, Mithat; Kaya, Ozlem; Yetkin, Elif Asli; Yetkin, Taylan; Cakir, Altan; Cankocak, Kerem; Sen, Sercan; Grynyov, Boris; Levchuk, Leonid; Sorokin, Pavel; Aggleton, Robin; Ball, Fionn; Beck, Lana; Brooke, James John; Burns, Douglas; Clement, Emyr; Cussans, David; Flacher, Henning; Goldstein, Joel; Grimes, Mark; Heath, Greg P; Heath, Helen F; Jacob, Jeson; Kreczko, Lukasz; Lucas, Chris; Newbold, Dave M; Paramesvaran, Sudarshan; Poll, Anthony; Sakuma, Tai; Seif El Nasr-storey, Sarah; Smith, Dominic; Smith, Vincent J; Bell, Ken W; Belyaev, Alexander; Brew, Christopher; Brown, Robert M; Calligaris, Luigi; Cieri, Davide; Cockerill, David JA; Coughlan, John A; Harder, Kristian; Harper, Sam; Olaiya, Emmanuel; Petyt, David; Shepherd-Themistocleous, Claire; Thea, Alessandro; Tomalin, Ian R; Williams, Thomas; Baber, Mark; Bainbridge, Robert; Buchmuller, Oliver; Bundock, Aaron; Burton, Darren; Casasso, Stefano; Citron, Matthew; Colling, David; Corpe, Louie; Dauncey, Paul; Davies, Gavin; De Wit, Adinda; Della Negra, Michel; Di Maria, Riccardo; Dunne, Patrick; Elwood, Adam; Futyan, David; Haddad, Yacine; Hall, Geoffrey; Iles, Gregory; James, Thomas; Lane, Rebecca; Laner, Christian; Lucas, Robyn; Lyons, Louis; Magnan, Anne-Marie; Malik, Sarah; Mastrolorenzo, Luca; Nash, Jordan; Nikitenko, Alexander; Pela, Joao; Penning, Bjoern; Pesaresi, Mark; Raymond, David Mark; Richards, Alexander; Rose, Andrew; Scott, Edward; Seez, Christopher; Summers, Sioni; Tapper, Alexander; Uchida, Kirika; Vazquez Acosta, Monica; Virdee, Tejinder; Wright, Jack; Zenz, Seth Conrad; Cole, Joanne; Hobson, Peter R; Khan, Akram; Kyberd, Paul; Reid, Ivan; Symonds, Philip; Teodorescu, Liliana; Turner, Mark; Borzou, Ahmad; Call, Kenneth; Dittmann, Jay; Hatakeyama, Kenichi; Liu, Hongxuan; Pastika, Nathaniel; Bartek, Rachel; Dominguez, Aaron; Buccilli, Andrew; Cooper, Seth; Henderson, Conor; Rumerio, Paolo; West, Christopher; Arcaro, Daniel; Avetisyan, Aram; Bose, Tulika; Gastler, Daniel; Rankin, Dylan; Richardson, Clint; Rohlf, James; Sulak, Lawrence; Zou, David; Benelli, Gabriele; Cutts, David; Garabedian, Alex; Hakala, John; Heintz, Ulrich; Hogan, Julie Managan; Jesus, Orduna; Kwok, Ka Hei Martin; Laird, Edward; Landsberg, Greg; Mao, Zaixing; Narain, Meenakshi; Piperov, Stefan; Sagir, Sinan; Spencer, Eric; Syarif, Rizki; Breedon, Richard; Burns, Dustin; Calderon De La Barca Sanchez, Manuel; Chauhan, Sushil; Chertok, Maxwell; Conway, John; Conway, Rylan; Cox, Peter Timothy; Erbacher, Robin; Flores, Chad; Funk, Garrett; Gardner, Michael; Ko, Winston; Lander, Richard; Mclean, Christine; Mulhearn, Michael; Pellett, Dave; Pilot, Justin; Shalhout, Shalhout; Shi, Mengyao; Smith, John; Squires, Michael; Stolp, Dustin; Tos, Kyle; Tripathi, Mani; Bachtis, Michail; Bravo, Cameron; Cousins, Robert; Dasgupta, Abhigyan; Florent, Alice; Hauser, Jay; Ignatenko, Mikhail; Mccoll, Nickolas; Saltzberg, David; Schnaible, Christian; Valuev, Vyacheslav; Weber, Matthias; Bouvier, Elvire; Burt, Kira; Clare, Robert; Ellison, John Anthony; Gary, J William; Ghiasi Shirazi, Seyyed Mohammad Amin; Hanson, Gail; Heilman, Jesse; Jandir, Pawandeep; Kennedy, Elizabeth; Lacroix, Florent; Long, Owen Rosser; Olmedo Negrete, Manuel; Paneva, Mirena Ivova; Shrinivas, Amithabh; Si, Weinan; Wei, Hua; Wimpenny, Stephen; Yates, Brent; Branson, James G; Cerati, Giuseppe Benedetto; Cittolin, Sergio; Derdzinski, Mark; Gerosa, Raffaele; Holzner, André; Klein, Daniel; Krutelyov, Vyacheslav; Letts, James; Macneill, Ian; Olivito, Dominick; Padhi, Sanjay; Pieri, Marco; Sani, Matteo; Sharma, Vivek; Simon, Sean; Tadel, Matevz; Vartak, Adish; Wasserbaech, Steven; Welke, Charles; Wood, John; Würthwein, Frank; Yagil, Avraham; Zevi Della Porta, Giovanni; Amin, Nick; Bhandari, Rohan; Bradmiller-Feld, John; Campagnari, Claudio; Dishaw, Adam; Dutta, Valentina; Franco Sevilla, Manuel; George, Christopher; Golf, Frank; Gouskos, Loukas; Gran, Jason; Heller, Ryan; Incandela, Joe; Mullin, Sam Daniel; Ovcharova, Ana; Qu, Huilin; Richman, Jeffrey; Stuart, David; Suarez, Indara; Yoo, Jaehyeok; Anderson, Dustin; Bendavid, Joshua; Bornheim, Adolf; Bunn, Julian; Duarte, Javier; Lawhorn, Jay Mathew; Mott, Alexander; Newman, Harvey B; Pena, Cristian; Spiropulu, Maria; Vlimant, Jean-Roch; Xie, Si; Zhu, Ren-Yuan; Andrews, Michael Benjamin; Ferguson, Thomas; Paulini, Manfred; Russ, James; Sun, Menglei; Vogel, Helmut; Vorobiev, Igor; Weinberg, Marc; Cumalat, John Perry; Ford, William T; Jensen, Frank; Johnson, Andrew; Krohn, Michael; Leontsinis, Stefanos; Mulholland, Troy; Stenson, Kevin; Wagner, Stephen Robert; Alexander, James; Chaves, Jorge; Chu, Jennifer; Dittmer, Susan; Mcdermott, Kevin; Mirman, Nathan; Nicolas Kaufman, Gala; Patterson, Juliet Ritchie; Rinkevicius, Aurelijus; Ryd, Anders; Skinnari, Louise; Soffi, Livia; Tan, Shao Min; Tao, Zhengcheng; Thom, Julia; Tucker, Jordan; Wittich, Peter; Zientek, Margaret; Winn, Dave; Abdullin, Salavat; Albrow, Michael; Apollinari, Giorgio; Apresyan, Artur; Banerjee, Sunanda; Bauerdick, Lothar AT; Beretvas, Andrew; Berryhill, Jeffrey; Bhat, Pushpalatha C; Bolla, Gino; Burkett, Kevin; Butler, Joel Nathan; Cheung, Harry; Chlebana, Frank; Cihangir, Selcuk; Cremonesi, Matteo; Elvira, Victor Daniel; Fisk, Ian; Freeman, Jim; Gottschalk, Erik; Gray, Lindsey; Green, Dan; Grünendahl, Stefan; Gutsche, Oliver; Hare, Daryl; Harris, Robert M; Hasegawa, Satoshi; Hirschauer, James; Hu, Zhen; Jayatilaka, Bodhitha; Jindariani, Sergo; Johnson, Marvin; Joshi, Umesh; Klima, Boaz; Kreis, Benjamin; Lammel, Stephan; Linacre, Jacob; Lincoln, Don; Lipton, Ron; Liu, Miaoyuan; Liu, Tiehui; Lopes De Sá, Rafael; Lykken, Joseph; Maeshima, Kaori; Magini, Nicolo; Marraffino, John Michael; Maruyama, Sho; Mason, David; McBride, Patricia; Merkel, Petra; Mrenna, Stephen; Nahn, Steve; O'Dell, Vivian; Pedro, Kevin; Prokofyev, Oleg; Rakness, Gregory; Ristori, Luciano; Sexton-Kennedy, Elizabeth; Soha, Aron; Spalding, William J; Spiegel, Leonard; Stoynev, Stoyan; Strait, James; Strobbe, Nadja; Taylor, Lucas; Tkaczyk, Slawek; Tran, Nhan Viet; Uplegger, Lorenzo; Vaandering, Eric Wayne; Vernieri, Caterina; Verzocchi, Marco; Vidal, Richard; Wang, Michael; Weber, Hannsjoerg Artur; Whitbeck, Andrew; Wu, Yujun; Acosta, Darin; Avery, Paul; Bortignon, Pierluigi; Bourilkov, Dimitri; Brinkerhoff, Andrew; Carnes, Andrew; Carver, Matthew; Curry, David; Das, Souvik; Field, Richard D; Furic, Ivan-Kresimir; Konigsberg, Jacobo; Korytov, Andrey; Low, Jia Fu; Ma, Peisen; Matchev, Konstantin; Mei, Hualin; Mitselmakher, Guenakh; Rank, Douglas; Shchutska, Lesya; Sperka, David; Thomas, Laurent; Wang, Jian; Wang, Sean-Jiun; Yelton, John; Linn, Stephan; Markowitz, Pete; Martinez, German; Rodriguez, Jorge Luis; Ackert, Andrew; Adams, Todd; Askew, Andrew; Bein, Samuel; Hagopian, Sharon; Hagopian, Vasken; Johnson, Kurtis F; Kolberg, Ted; Perry, Thomas; Prosper, Harrison; Santra, Arka; Yohay, Rachel; Baarmand, Marc M; Bhopatkar, Vallary; Colafranceschi, Stefano; Hohlmann, Marcus; Noonan, Daniel; Roy, Titas; Yumiceva, Francisco; Adams, Mark Raymond; Apanasevich, Leonard; Berry, Douglas; Betts, Russell Richard; Bucinskaite, Inga; Cavanaugh, Richard; Chen, Xuan; Evdokimov, Olga; Gauthier, Lucie; Gerber, Cecilia Elena; Hofman, David Jonathan; Jung, Kurt; Sandoval Gonzalez, Irving Daniel; Varelas, Nikos; Wang, Hui; Wu, Zhenbin; Zakaria, Mohammed; Zhang, Jingyu; Bilki, Burak; Clarida, Warren; Dilsiz, Kamuran; Durgut, Süleyman; Gandrajula, Reddy Pratap; Haytmyradov, Maksat; Khristenko, Viktor; Merlo, Jean-Pierre; Mermerkaya, Hamit; Mestvirishvili, Alexi; Moeller, Anthony; Nachtman, Jane; Ogul, Hasan; Onel, Yasar; Ozok, Ferhat; Penzo, Aldo; Snyder, Christina; Tiras, Emrah; Wetzel, James; Yi, Kai; Blumenfeld, Barry; Cocoros, Alice; Eminizer, Nicholas; Fehling, David; Feng, Lei; Gritsan, Andrei; Maksimovic, Petar; Roskes, Jeffrey; Sarica, Ulascan; Swartz, Morris; Xiao, Meng; You, Can; Al-bataineh, Ayman; Baringer, Philip; Bean, Alice; Boren, Samuel; Bowen, James; Castle, James; Forthomme, Laurent; Kenny III, Raymond Patrick; Khalil, Sadia; Kropivnitskaya, Anna; Majumder, Devdatta; Mcbrayer, William; Murray, Michael; Sanders, Stephen; Stringer, Robert; Tapia Takaki, Daniel; Wang, Quan; Ivanov, Andrew; Kaadze, Ketino; Maravin, Yurii; Mohammadi, Abdollah; Saini, Lovedeep Kaur; Skhirtladze, Nikoloz; Toda, Sachiko; Rebassoo, Finn; Wright, Douglas; Anelli, Christopher; Baden, Drew; Baron, Owen; Belloni, Alberto; Calvert, Brian; Eno, Sarah Catherine; Ferraioli, Charles; Gomez, Jaime; Hadley, Nicholas John; Jabeen, Shabnam; Jeng, Geng-Yuan; Kellogg, Richard G; Kunkle, Joshua; Mignerey, Alice; Ricci-Tam, Francesca; Shin, Young Ho; Skuja, Andris; Tonjes, Marguerite; Tonwar, Suresh C; Abercrombie, Daniel; Allen, Brandon; Apyan, Aram; Azzolini, Virginia; Barbieri, Richard; Baty, Austin; Bi, Ran; Bierwagen, Katharina; Brandt, Stephanie; Busza, Wit; Cali, Ivan Amos; D'Alfonso, Mariarosaria; Demiragli, Zeynep; Gomez Ceballos, Guillelmo; Goncharov, Maxim; Hsu, Dylan; Iiyama, Yutaro; Innocenti, Gian Michele; Klute, Markus; Kovalskyi, Dmytro; Krajczar, Krisztian; Lai, Yue Shi; Lee, Yen-Jie; Levin, Andrew; Luckey, Paul David; Maier, Benedikt; Marini, Andrea Carlo; Mcginn, Christopher; Mironov, Camelia; Narayanan, Siddharth; Niu, Xinmei; Paus, Christoph; Roland, Christof; Roland, Gunther; Salfeld-Nebgen, Jakob; Stephans, George; Tatar, Kaya; Velicanu, Dragos; Wang, Jing; Wang, Ta-Wei; Wyslouch, Bolek; Benvenuti, Alberto; Chatterjee, Rajdeep Mohan; Evans, Andrew; Hansen, Peter; Kalafut, Sean; Kao, Shih-Chuan; Kubota, Yuichi; Lesko, Zachary; Mans, Jeremy; Nourbakhsh, Shervin; Ruckstuhl, Nicole; Rusack, Roger; Tambe, Norbert; Turkewitz, Jared; Acosta, John Gabriel; Oliveros, Sandra; Avdeeva, Ekaterina; Bloom, Kenneth; Claes, Daniel R; Fangmeier, Caleb; Gonzalez Suarez, Rebeca; Kamalieddin, Rami; Kravchenko, Ilya; Malta Rodrigues, Alan; Monroy, Jose; Siado, Joaquin Emilo; Snow, Gregory R; Stieger, Benjamin; Alyari, Maral; Dolen, James; Godshalk, Andrew; Harrington, Charles; Iashvili, Ia; Kaisen, Josh; Nguyen, Duong; Parker, Ashley; Rappoccio, Salvatore; Roozbahani, Bahareh; Alverson, George; Barberis, Emanuela; Hortiangtham, Apichart; Massironi, Andrea; Morse, David Michael; Nash, David; Orimoto, Toyoko; Teixeira De Lima, Rafael; Trocino, Daniele; Wang, Ren-Jie; Wood, Darien; Bhattacharya, Saptaparna; Charaf, Otman; Hahn, Kristan Allan; Kumar, Ajay; Mucia, Nicholas; Odell, Nathaniel; Pollack, Brian; Schmitt, Michael Henry; Sung, Kevin; Trovato, Marco; Velasco, Mayda; Dev, Nabarun; Hildreth, Michael; Hurtado Anampa, Kenyi; Jessop, Colin; Karmgard, Daniel John; Kellams, Nathan; Lannon, Kevin; Marinelli, Nancy; Meng, Fanbo; Mueller, Charles; Musienko, Yuri; Planer, Michael; Reinsvold, Allison; Ruchti, Randy; Rupprecht, Nathaniel; Smith, Geoffrey; Taroni, Silvia; Wayne, Mitchell; Wolf, Matthias; Woodard, Anna; Alimena, Juliette; Antonelli, Louis; Bylsma, Ben; Durkin, Lloyd Stanley; Flowers, Sean; Francis, Brian; Hart, Andrew; Hill, Christopher; Ji, Weifeng; Liu, Bingxuan; Luo, Wuming; Puigh, Darren; Winer, Brian L; Wulsin, Howard Wells; Cooperstein, Stephane; Driga, Olga; Elmer, Peter; Hardenbrook, Joshua; Hebda, Philip; Lange, David; Luo, Jingyu; Marlow, Daniel; Medvedeva, Tatiana; Mei, Kelvin; Ojalvo, Isabel; Olsen, James; Palmer, Christopher; Piroué, Pierre; Stickland, David; Svyatkovskiy, Alexey; Tully, Christopher; Malik, Sudhir; Barker, Anthony; Barnes, Virgil E; Folgueras, Santiago; Gutay, Laszlo; Jha, Manoj; Jones, Matthew; Jung, Andreas Werner; Khatiwada, Ajeeta; Miller, David Harry; Neumeister, Norbert; Schulte, Jan-Frederik; Shi, Xin; Sun, Jian; Wang, Fuqiang; Xie, Wei; Parashar, Neeti; Stupak, John; Adair, Antony; Akgun, Bora; Chen, Zhenyu; Ecklund, Karl Matthew; Geurts, Frank JM; Guilbaud, Maxime; Li, Wei; Michlin, Benjamin; Northup, Michael; Padley, Brian Paul; Roberts, Jay; Rorie, Jamal; Tu, Zhoudunming; Zabel, James; Betchart, Burton; Bodek, Arie; de Barbaro, Pawel; Demina, Regina; Duh, Yi-ting; Ferbel, Thomas; Galanti, Mario; Garcia-Bellido, Aran; Han, Jiyeon; Hindrichs, Otto; Khukhunaishvili, Aleko; Lo, Kin Ho; Tan, Ping; Verzetti, Mauro; Ciesielski, Robert; Agapitos, Antonis; Chou, John Paul; Gershtein, Yuri; Gómez Espinosa, Tirso Alejandro; Halkiadakis, Eva; Heindl, Maximilian; Hughes, Elliot; Kaplan, Steven; Kunnawalkam Elayavalli, Raghav; Kyriacou, Savvas; Lath, Amitabh; Nash, Kevin; Osherson, Marc; Saka, Halil; Salur, Sevil; Schnetzer, Steve; Sheffield, David; Somalwar, Sunil; Stone, Robert; Thomas, Scott; Thomassen, Peter; Walker, Matthew; Delannoy, Andrés G; Foerster, Mark; Heideman, Joseph; Riley, Grant; Rose, Keith; Spanier, Stefan; Thapa, Krishna; Bouhali, Othmane; Celik, Ali; Dalchenko, Mykhailo; De Mattia, Marco; Delgado, Andrea; Dildick, Sven; Eusebi, Ricardo; Gilmore, Jason; Huang, Tao; Juska, Evaldas; Kamon, Teruki; Mueller, Ryan; Pakhotin, Yuriy; Patel, Rishi; Perloff, Alexx; Perniè, Luca; Rathjens, Denis; Safonov, Alexei; Tatarinov, Aysen; Ulmer, Keith; Akchurin, Nural; Damgov, Jordan; De Guio, Federico; Dragoiu, Cosmin; Dudero, Phillip Russell; Faulkner, James; Gurpinar, Emine; Kunori, Shuichi; Lamichhane, Kamal; Lee, Sung Won; Libeiro, Terence; Peltola, Timo; Undleeb, Sonaina; Volobouev, Igor; Wang, Zhixing; Greene, Senta; Gurrola, Alfredo; Janjam, Ravi; Johns, Willard; Maguire, Charles; Melo, Andrew; Ni, Hong; Sheldon, Paul; Tuo, Shengquan; Velkovska, Julia; Xu, Qiao; Arenton, Michael Wayne; Barria, Patrizia; Cox, Bradley; Goodell, Joseph; Hirosky, Robert; Ledovskoy, Alexander; Li, Hengne; Neu, Christopher; Sinthuprasith, Tutanon; Sun, Xin; Wang, Yanchu; Wolfe, Evan; Xia, Fan; Clarke, Christopher; Harr, Robert; Karchin, Paul Edmund; Sturdy, Jared; Zaleski, Shawn; Belknap, Donald; Buchanan, James; Caillol, Cécile; Dasu, Sridhara; Dodd, Laura; Duric, Senka; Gomber, Bhawna; Grothe, Monika; Herndon, Matthew; Hervé, Alain; Klabbers, Pamela; Lanaro, Armando; Levine, Aaron; Long, Kenneth; Loveless, Richard; Pierro, Giuseppe Antonio; Polese, Giovanni; Ruggles, Tyler; Savin, Alexander; Smith, Nicholas; Smith, Wesley H; Taylor, Devin; Woods, Nathaniel

    2017-01-01

    Events with no charged particles produced between the two leading jets are studied in proton-proton collisions at $\\sqrt{s}= $ 7 TeV. The jets were required to have transverse momentum ${p_{\\mathrm{T}}}^{\\text{jet}} > $ 40 GeV and pseudorapidity 1.5 $ $ 0.2 GeV in the interval $-1 < \\eta < 1$ between the jets are observed in excess of calculations that assume no color-singlet exchange. The fraction of events with such a rapidity gap, amounting to 0.5-1% of the selected dijet sample, is measured as a function of the ${p_{\\mathrm{T}}}$ of the second-leading jet and of the rapidity separation between the jets. The data are compared to previous measurements at Tevatron, and to perturbative quantum chromodynamics calculations based on the Balitsky-Fadin-Kuraev-Lipatov evolution equations, including different modelings of the non-perturbative gap survival probability. (We dedicate this paper to the memory of our colleague and friend Sasha Proskuryakov, who started this analysis but passed away before it was ...

  18. Discoveries of isotopes by fission

    Indian Academy of Sciences (India)

    M Thoennessen

    2015-09-01

    Of the about 3000 isotopes presently known, about 20% have been discovered in fission. The history of fission as it relates to the discovery of isotopes as well as the various reaction mechanisms leading to isotope discoveries involving fission are presented.

  19. Determining lead sources in Mexico using the lead isotope ratio La identificación de fuentes de exposición a plomo en México a través de la determinación de la razón de isótopos de plomo

    Directory of Open Access Journals (Sweden)

    Madhu Chaudhary-Webb

    2003-01-01

    Full Text Available OBJECTIVE: Lead poisoning can, in some cases, be traced to a specific route or source of exposure on the basis of the individual's blood lead isotope ratio. To assess the major source of lead exposure among women residing in Mexico City, we compared blood, ceramic, and gasoline lead isotope ratios. MATERIAL AND METHODS: The study population, randomly selected from participants of a large trial, (1/1996-12/1996 comprised of 16 women whose lead levels exceeded 10 µg/dl and who reported using lead-glazed ceramics. Lead isotope ratios were performed on a Perkin Elmer 5000 Inductively Coupled Plasma Mass Spectrometer (ICP-MS interfaced with a Perkin Elmer HGA-600MS Electrothermal Vaporization System (ETV. RESULTS: The isotope ratios (206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb of both the blood specimens and their corresponding ceramic specimens were highly correlated, with r=0.9979, r²=0.9958, r=0.9957, r²=0.9915 and r=0.9945, r²=0.9890 values for the three isotope ratios, respectively, suggesting that the lead exposure most likely resulted from the use of these ceramic. Measurements of lead isotope ratios from leaded gasoline in use at the time of blood sampling, differed from those in blood and ceramics. CONCLUSIONS: Determining lead isotope ratios can be an efficient tool to identify a major source of lead exposure and to support the implementation of public health prevention and control measures.OBJETIVO: Identificar la fuente principal de exposición a plomo entre mujeres residentes en la Ciudad de México, por medio de la comparación de las razones de isótopos de plomo en sangre, cerámica y gasolina. MATERIAL Y MÉTODOS: La población de estudio fue seleccionada aleatoriamente de participantes de una muestra obtenida de enero a diciembre de 1996 y consistió en 16 mujeres con niveles de plomo mayores a 10 µg/dl, que usaban cerámica vidriada con plomo. Las razones de isótopos de plomo se obtuvieron con un espectrómetro de masa de

  20. A Portable and Power-Free Microfluidic Device for Rapid and Sensitive Lead (Pb2+ Detection

    Directory of Open Access Journals (Sweden)

    Lianhui Wang

    2012-07-01

    Full Text Available A portable and power-free microfluidic device was designed for rapid and sensitive detection of lead (Pb2+. 11-mercaptoundecanoic acid (MUA-functionalized gold nanoparticles (MUA-AuNPs aggregated in the presence of Pb2+ for the chelation mechanism. When we performed this analysis on a polydimethylsiloxane (PDMS microfluidic chip, the aggregations deposited onto the surface of chip and formed dark lines along the laminar flows in the zigzag microchannels. This visual result can be observed by the naked eye through a microscope or just a drop of water as a magnifier. Ten μM Pb2+ was successfully detected.

  1. Centrality, rapidity and transverse momentum dependence of isolated prompt photon production in lead-lead collisions at $\\sqrt{s_{\\mathrm{NN}}} = 2.76$ TeV measured with the ATLAS detector

    CERN Document Server

    Aad, Georges; Abdallah, Jalal; Abdel Khalek, Samah; Abdinov, Ovsat; Aben, Rosemarie; Abi, Babak; Abolins, Maris; AbouZeid, Ossama; Abramowicz, Halina; Abreu, Henso; Abreu, Ricardo; Abulaiti, Yiming; Acharya, Bobby Samir; Adamczyk, Leszek; Adams, David; Adelman, Jahred; Adomeit, Stefanie; Adye, Tim; Agatonovic-Jovin, Tatjana; Aguilar-Saavedra, Juan Antonio; Agustoni, Marco; Ahlen, Steven; Ahmadov, Faig; Aielli, Giulio; Akerstedt, Henrik; Åkesson, Torsten Paul Ake; Akimoto, Ginga; Akimov, Andrei; Alberghi, Gian Luigi; Albert, Justin; Albrand, Solveig; Alconada Verzini, Maria Josefina; Aleksa, Martin; Aleksandrov, Igor; Alexa, Calin; Alexander, Gideon; Alexandre, Gauthier; Alexopoulos, Theodoros; Alhroob, Muhammad; Alimonti, Gianluca; Alio, Lion; Alison, John; Allbrooke, Benedict; Allison, Lee John; Allport, Phillip; Almond, John; Aloisio, Alberto; Alonso, Alejandro; Alonso, Francisco; Alpigiani, Cristiano; Altheimer, Andrew David; Alvarez Gonzalez, Barbara; Alviggi, Mariagrazia; Amako, Katsuya; Amaral Coutinho, Yara; Amelung, Christoph; Amidei, Dante; Amor Dos Santos, Susana Patricia; Amorim, Antonio; Amoroso, Simone; Amram, Nir; Amundsen, Glenn; Anastopoulos, Christos; Ancu, Lucian Stefan; Andari, Nansi; Andeen, Timothy; Anders, Christoph Falk; Anders, Gabriel; Anderson, Kelby; Andreazza, Attilio; Andrei, George Victor; Anduaga, Xabier; Angelidakis, Stylianos; Angelozzi, Ivan; Anger, Philipp; Angerami, Aaron; Anghinolfi, Francis; Anisenkov, Alexey; Anjos, Nuno; Annovi, Alberto; Antonaki, Ariadni; Antonelli, Mario; Antonov, Alexey; Antos, Jaroslav; Anulli, Fabio; Aoki, Masato; Aperio Bella, Ludovica; Apolle, Rudi; Arabidze, Giorgi; Aracena, Ignacio; Arai, Yasuo; Araque, Juan Pedro; Arce, Ayana; Arguin, Jean-Francois; Argyropoulos, Spyridon; Arik, Metin; Armbruster, Aaron James; Arnaez, Olivier; Arnal, Vanessa; Arnold, Hannah; Arratia, Miguel; Arslan, Ozan; Artamonov, Andrei; Artoni, Giacomo; Asai, Shoji; Asbah, Nedaa; Ashkenazi, Adi; Åsman, Barbro; Asquith, Lily; Assamagan, Ketevi; Astalos, Robert; Atkinson, Markus; Atlay, Naim Bora; Auerbach, Benjamin; Augsten, Kamil; Aurousseau, Mathieu; Avolio, Giuseppe; Azuelos, Georges; Azuma, Yuya; Baak, Max; Baas, Alessandra; Bacci, Cesare; Bachacou, Henri; Bachas, Konstantinos; Backes, Moritz; Backhaus, Malte; Backus Mayes, John; Badescu, Elisabeta; Bagiacchi, Paolo; Bagnaia, Paolo; Bai, Yu; Bain, Travis; Baines, John; Baker, Oliver Keith; Balek, Petr; Balli, Fabrice; Banas, Elzbieta; Banerjee, Swagato; Bannoura, Arwa A E; Bansal, Vikas; Bansil, Hardeep Singh; Barak, Liron; Barberio, Elisabetta Luigia; Barberis, Dario; Barbero, Marlon; Barillari, Teresa; Barisonzi, Marcello; Barklow, Timothy; Barlow, Nick; Barnett, Bruce; Barnett, Michael; Barnovska, Zuzana; Baroncelli, Antonio; Barone, Gaetano; Barr, Alan; Barreiro, Fernando; Barreiro Guimarães da Costa, João; Bartoldus, Rainer; Barton, Adam Edward; Bartos, Pavol; Bartsch, Valeria; Bassalat, Ahmed; Basye, Austin; Bates, Richard; Batley, Richard; Battaglia, Marco; Battistin, Michele; Bauer, Florian; Bawa, Harinder Singh; Beattie, Michael David; Beau, Tristan; Beauchemin, Pierre-Hugues; Beccherle, Roberto; Bechtle, Philip; Beck, Hans Peter; Becker, Anne Kathrin; Becker, Sebastian; Beckingham, Matthew; Becot, Cyril; Beddall, Andrew; Beddall, Ayda; Bedikian, Sourpouhi; Bednyakov, Vadim; Bee, Christopher; Beemster, Lars; Beermann, Thomas; Begel, Michael; Behr, Janna Katharina; Belanger-Champagne, Camille; Bell, Paul; Bell, William; Bella, Gideon; Bellagamba, Lorenzo; Bellerive, Alain; Bellomo, Massimiliano; Belotskiy, Konstantin; Beltramello, Olga; Benary, Odette; Benchekroun, Driss; Bendtz, Katarina; Benekos, Nektarios; Benhammou, Yan; Benhar Noccioli, Eleonora; Benitez Garcia, Jorge-Armando; Benjamin, Douglas; Bensinger, James; Benslama, Kamal; Bentvelsen, Stan; Berge, David; Bergeaas Kuutmann, Elin; Berger, Nicolas; Berghaus, Frank; Beringer, Jürg; Bernard, Clare; Bernat, Pauline; Bernius, Catrin; Bernlochner, Florian Urs; Berry, Tracey; Berta, Peter; Bertella, Claudia; Bertoli, Gabriele; Bertolucci, Federico; Bertsche, Carolyn; Bertsche, David; Besana, Maria Ilaria; Besjes, Geert-Jan; Bessidskaia Bylund, Olga; Bessner, Martin Florian; Besson, Nathalie; Betancourt, Christopher; Bethke, Siegfried; Bhimji, Wahid; Bianchi, Riccardo-Maria; Bianchini, Louis; Bianco, Michele; Biebel, Otmar; Bieniek, Stephen Paul; Bierwagen, Katharina; Biesiada, Jed; Biglietti, Michela; Bilbao De Mendizabal, Javier; Bilokon, Halina; Bindi, Marcello; Binet, Sebastien; Bingul, Ahmet; Bini, Cesare; Black, Curtis; Black, James; Black, Kevin

    2016-01-01

    Prompt photon production in $\\sqrt{s_{\\mathrm{NN}}} = 2.76$ TeV Pb+Pb collisions has been measured by the ATLAS experiment at the Large Hadron Collider using data collected in 2011 with an integrated luminosity of 0.14 nb$^{-1}$. Inclusive photon yields, scaled by the mean nuclear thickness function, are presented as a function of collision centrality and transverse momentum in two pseudo rapidity intervals, $|\\eta| < 1.37$ and $1.52 < |\\eta| < 2.37$. The scaled yields in the two pseudorapidity intervals, as well as the ratios of the forward yields to those at midrapidity, are compared to the expectations from next-to-leading order perturbative QCD calculations from JETPHOX. The measured cross sections agree well with the predictions for proton-proton collisions within statistical and systematic uncertainties. Both the yields and ratios are also compared to two other pQCD calculations, one which uses the isospin content appropriate to colliding lead nuclei, and another which includes the EPS09 nuclea...

  2. Evaluation of laser ablation double-focusing SC-ICPMS for “common” lead isotopic measurements in silicate glasses and mineral

    Science.gov (United States)

    Pietruszka, Aaron J.; Neymark, Leonid

    2017-01-01

    An analytical method for the in situ measurement of “common” Pb isotope ratios in silicate glasses and minerals using a 193-nm excimer laser ablation (LA) system with a double-focusing single-collector (SC)-ICPMS is presented and evaluated as a possible alternative to multiple-collector (MC)-ICPMS. This LA-SC-ICPMS technique employs fast-scanning ion deflectors to sequentially place a series of flat-topped isotope peaks into a single ion-counting detector at a fixed accelerating voltage and magnetic field strength. Reference materials (including NIST, MPI-DING, and USGS glasses) are used to identify two analytical artifacts on the Pb isotope ratios (expressed here as heavier/lighter isotopes) when corrected for mass bias relative to NIST SRM610. The first artifact is characterized by anomalously low Pb isotope ratios (~0.1%/AMU) when SRM610 is analyzed in raster mode as an unknown at small spot sizes (materials (BCR-2G, GOR132-G, and T1-G). These offsets are thought to be caused by one or more non-spectral matrix effects related to differences in the ablation behavior, composition, or physical properties of these reference materials compared to the bracketing SRM610 standard. The precision (±2SD) of our LA-SC-ICPMS Pb isotopic measurements is similar to (207Pb/206Pb and 208Pb/206Pb, or 20XPb/206Pb) or better than (206Pb/204Pb,207Pb/204Pb, and 208Pb/204Pb, or 20XPb/204Pb) a series of published studies that used a different type of SC-ICPMS and obtained a factor of ~3-4 higher sensitivity for Pb. An increase in the sensitivity of our LA-SC-ICPMS would likely improve the precision of the 20XPb/206Pb and 20XPb/204Pb ratios for low-Pb materials (making the technique broadly similar to LA-MC-ICPMS (particularly compared to methods that rely upon at least one ion-counting detector). Further improvement in the precision of the 20XPb/206Pb and 20XPb/204Pb ratios for high-Pb materials (>5 ppm) by LA-SC-ICPMS is unlikely, and in this case, LA-MC-ICPMS remains the

  3. Isotopes in Greenland Precipitation

    DEFF Research Database (Denmark)

    Faber, Anne-Katrine

    Greenland ice cores offer a unique opportunity to investigate the climate system behaviour. The objective of this PhD project is to investigate isotope modelling of present- day conditions and conduct model-data comparison using Greenland ice cores. Thus this thesis investigates how the integration...... of model and data can be used to improve the understanding of climate changes. This is done through analysis of isotope modelling, observations and ice core measurements. This dissertation comprises three projects: (1) Modelling the isotopic response to changes in Arctic sea surface conditions, (2......) Constructing a new Greenland database of observations and present-day ice core measurements, and (3) Performance test of isotope-enabled CAM5 for Greenland. The recent decades of rapid Arctic sea ice decline are used as a basis for an observational-based model experiment using the isotope-enabled CAM model 3...

  4. Direct lead isotope analysis in Hg-rich sulfides by LA-MC-ICP-MS with a gas exchange device and matrix-matched calibration.

    Science.gov (United States)

    Zhang, Wen; Hu, Zhaochu; Günther, Detlef; Liu, Yongsheng; Ling, Wenli; Zong, Keqing; Chen, Haihong; Gao, Shan

    2016-12-15

    In situ Pb isotope data of sulfide samples measured by LA-MC-ICP-MS provide valuable geochemical information for studies of the origin and evolution of ore deposits. However, the severe isobaric interference of (204)Hg on (204)Pb and the lack of matrix-matched sulfide reference materials limit the precision of Pb isotopic analyses for Hg-rich sulfides. In this study, we observe that Hg forms vapor and can be completely removed from sample aerosol particles produced by laser ablation using a gas exchange device. Additionally, this device does not influence the signal intensities of Pb isotopes. The within-run precision, the external reproducibility and the analytical accuracy are significantly improved for the Hg-rich sulfide samples using this mercury-vapor-removing device. Matrix effects are observed when using silicate glass reference materials as the external standards to assess the relationship of mass fractionation factors between Tl and Pb in sulfide samples, resulting in a maximum deviation of ∼0.20% for (20x)Pb/(204)Pb. Matrix-matched reference materials are therefore required for the highly precise and accurate Pb isotope analyses of sulfide samples. We investigated two sulfide samples, MASS-1 (the Unites States Geological Survey reference materials) and Sph-HYLM (a natural sphalerite), as potential candidates. Repeated analyses of the two proposed sulfide reference materials by LA-MC-ICP-MS yield good external reproducibility of ICP-MS, demonstrating the reliability and robustness of our analytical protocol. Copyright © 2016 Elsevier B.V. All rights reserved.

  5. High-precision analysis on annual variations of heavy metals, lead isotopes and rare earth elements in mangrove tree rings by inductively coupled plasma mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Yu Kefu [South China Sea Institute of Oceanology, Chinese Academy of Sciences, 164 West Xin-Gang Road, Guangzhou 510301 (China) and Radiogenic Isotope Laboratory, Centre for Microscopy and Microanalysis (CMM), University of Queensland, Qld 4072 (Australia)]. E-mail: kefuyu@scsio.ac.cn; Kamber, Balz S. [Radiogenic Isotope Laboratory, Centre for Microscopy and Microanalysis (CMM), University of Queensland, Qld 4072 (Australia); Department of Earth Sciences, Laurentian University, Sudbury, ONP3E2C6 (Canada); Lawrence, Michael G. [Radiogenic Isotope Laboratory, Centre for Microscopy and Microanalysis (CMM), University of Queensland, Qld 4072 (Australia); Greig, Alan [Radiogenic Isotope Laboratory, Centre for Microscopy and Microanalysis (CMM), University of Queensland, Qld 4072 (Australia); School of Earth Sciences, University of Melbourne, Vic. 3010 (Australia); Zhao Jianxin [Radiogenic Isotope Laboratory, Centre for Microscopy and Microanalysis (CMM), University of Queensland, Qld 4072 (Australia)

    2007-02-15

    Annual variations from 1982 to 1999 of a wide range of trace elements and reconnaissance Pb isotopes ({sup 207}Pb/{sup 206}Pb and {sup 208}Pb/{sup 206}Pb) were analyzed by solution ICP-MS on digested ash from mangrove Rhizophora apiculata, obtained from Leizhou Peninsula, along northern coast of South China Sea. The concentrations of the majority of elements show a weak declining trend with growth from 1982 to 1999, punctuated by several high concentration spikes. The declining trends are positively correlated with ring width and negatively correlated with inferred water-use efficiency, suggesting a physiological control over metal-uptake in this species. The episodic metal concentration-peaks cannot be interpreted with lateral movement or growth activities and appear to be related to environmental pollution events. Pb isotope ratios for most samples plot along the 'Chinese Pb line' and clearly document the importance of gasoline Pb as a source of contaminant. Shale-normalised REE + Y patterns are relatively flat and consistent across the growth period, with all patterns showing a positive Ce anomaly and elevated Y/Ho ratio. The positive Ce anomaly is observed regardless of the choice of normaliser, in contrast to previously reported REE patterns for terrestrial and marine plants. This pilot study of trace element, REE + Y and Pb isotope distribution in mangrove tree rings indicates the potential use of mangroves as monitors of historical environmental change.

  6. High-precision analysis on annual variations of heavy metals, lead isotopes and rare earth elements in mangrove tree rings by inductively coupled plasma mass spectrometry

    Science.gov (United States)

    Yu, Ke-Fu; Kamber, Balz S.; Lawrence, Michael G.; Greig, Alan; Zhao, Jian-Xin

    2007-02-01

    Annual variations from 1982 to 1999 of a wide range of trace elements and reconnaissance Pb isotopes ( 207Pb/ 206Pb and 208Pb/ 206Pb) were analyzed by solution ICP-MS on digested ash from mangrove Rhizophora apiculata, obtained from Leizhou Peninsula, along northern coast of South China Sea. The concentrations of the majority of elements show a weak declining trend with growth from 1982 to 1999, punctuated by several high concentration spikes. The declining trends are positively correlated with ring width and negatively correlated with inferred water-use efficiency, suggesting a physiological control over metal-uptake in this species. The episodic metal concentration-peaks cannot be interpreted with lateral movement or growth activities and appear to be related to environmental pollution events. Pb isotope ratios for most samples plot along the 'Chinese Pb line' and clearly document the importance of gasoline Pb as a source of contaminant. Shale-normalised REE + Y patterns are relatively flat and consistent across the growth period, with all patterns showing a positive Ce anomaly and elevated Y/Ho ratio. The positive Ce anomaly is observed regardless of the choice of normaliser, in contrast to previously reported REE patterns for terrestrial and marine plants. This pilot study of trace element, REE + Y and Pb isotope distribution in mangrove tree rings indicates the potential use of mangroves as monitors of historical environmental change.

  7. Lead as transient geochemical tracers in the environment: Assessing high precision isotope ratio measurements in lichens, peat, and silicates using multi-collector ICP-MS

    Science.gov (United States)

    Weiss, D. J.; Kober, B.; Mason, T. F.; Dolgopolova, A.; Coles, B. J.; Gallagher, K.; Leroux, G.; Spiro, B.; Seltmann, R.

    2003-04-01

    In recent years, MC-ICP-MS has become a powerful tool to measure Pb isotopes with high precision and accuracy. Yet, this technique is still relatively new, and the complexities related to using an ICP ion source for high precision isotope measurements are only now becoming apparent. In addition, most analytical development work so far has focussed on synthetic solutions and silicate material. Given the great importance of Pb isotopes in environmental geochemical studies, however, a careful assessment of analytical procedures for environmental samples is clearly needed and warranted. Consequently, we present here a study of the analytical performance of the Imperial College/Natural History Museum (IC/NHM) IsoProbe MC-ICPMS with respect to high precision Pb isotope measurements in peat, lichen and silicates. After acid digestion, the samples were passed through an exchange column using a new procedure developed at the University of Heidelberg (Kober, in prep.). This chemistry yielded quantitative recoveries and allowed a high sample throughput as only one column passage was needed to achieve stable ion beam signals. Selected samples were also analysed on a Finnegan MAT261 TIMS. Typical internal precisions of 10-35 ppm (1se) were achieved on all Pb isotope ratios in all matrices. Measurements of Pb 981 NIST standards spiked with Tl 997 NIST showed that the certified NBS Tl ratio had to be adjusted daily up to 2.38993 in order to obtain accurate data. The reproducibility for the synthetic standard over a three month period using daily optimised Tl values (but with no 2σ outlier rejection routine applied) was below 300 ppm for all ratios (including the 208Pb/204Pb ratio). On peak zeroing (OPZ) and half mass baseline correction procedures gave similar precisions. However, the accuracies on the 204 ratios were significantly worse using half mass baseline correction for Pb/Tl ratios less than 2. This behaviour is consistent with tailing of 205Tl onto the 204Pb peak

  8. Pb-Sr isotopic and geochemical constraints on sources and processes of lead contamination in well waters and soil from former fruit orchards, Pennsylvania, USA: A legacy of anthropogenic activities

    Science.gov (United States)

    Ayuso, Robert A.; Foley, Nora K.

    2016-01-01

    Isotopic discrimination can be an effective tool in establishing a direct link between sources of Pb contamination and the presence of anomalously high concentrations of Pb in waters, soils, and organisms. Residential wells supplying water containing up to 1600 ppb Pb to houses built on the former Mohr orchards commercial site, near Allentown, PA, were evaluated to discern anthropogenic from geogenic sources. Pb (n = 144) and Sr (n = 40) isotopic data and REE (n = 29) data were determined for waters from residential wells, test wells (drilled for this study), and surface waters from pond and creeks. Local soils, sediments, bedrock, Zn-Pb mineralization and coal were also analyzed (n = 94), together with locally used Pb-As pesticide (n = 5). Waters from residential and test wells show overlapping values of 206Pb/207Pb, 208Pb/207Pb and 87Sr/86Sr. Larger negative Ce anomalies (Ce/Ce*) distinguish residential wells from test wells. Results show that residential and test well waters, sediments from residential water filters in water tanks, and surface waters display broad linear trends in Pb isotope plots. Pb isotope data for soils, bedrock, and pesticides have contrasting ranges and overlapping trends. Contributions of Pb from soils to residential well waters are limited and implicated primarily in wells having shallow water-bearing zones and carrying high sediment contents. Pb isotope data for residential wells, test wells, and surface waters show substantial overlap with Pb data reflecting anthropogenic actions (e.g., burning fossil fuels, industrial and urban processing activities). Limited contributions of Pb from bedrock, soils, and pesticides are evident. High Pb concentrations in the residential waters are likely related to sediment build up in residential water tanks. Redox reactions, triggered by influx of groundwater via wells into the residential water systems and leading to subtle changes in pH, are implicated in precipitation of Fe oxyhydroxides

  9. 夏商周青铜器铅同位素示踪研究数据库的构建%A Lead Isotope Ratio Data Base of Ancient Chinese Bronzes

    Institute of Scientific and Technical Information of China (English)

    金正耀

    2005-01-01

    A data base of lead isotope ratio of ancient Chinese bronzes is set up. There are 2 888 members, including bronze objects, casting remains, and related ores, etc. in the file. The file contents of data base are made from analysis work on Chinese bronze previously carried out in several laboratories in China, Japan and USA. The main body of the file contents is formed from records, analysis data, reference documents, and images. The data base is designed for sharing information in provenance study on raw metal material for bronze production in China Bronze Age.

  10. Rapid 'de novo' peptide sequencing by a combination of nanoelectrospray, isotopic labeling and a quadrupole/time-of-flight mass spectrometer.

    Science.gov (United States)

    Shevchenko, A; Chernushevich, I; Ens, W; Standing, K G; Thomson, B; Wilm, M; Mann, M

    1997-01-01

    Protein microanalysis usually involves the sequencing of gel-separated proteins available in very small amounts. While mass spectrometry has become the method of choice for identifying proteins in databases, in almost all laboratories 'de novo' protein sequencing is still performed by Edman degradation. Here we show that a combination of the nanoelectrospray ion source, isotopic end labeling of peptides and a quadrupole/ time-of-flight instrument allows facile read-out of the sequences of tryptic peptides. Isotopic labeling was performed by enzymatic digestion of proteins in 1:1 16O/18O water, eliminating the need for peptide derivatization. A quadrupole/time-of-flight mass spectrometer was constructed from a triple quadrupole and an electrospray time-of-flight instrument. Tandem mass spectra of peptides were obtained with better than 50 ppm mass accuracy and resolution routinely in excess of 5000. Unique and error tolerant identification of yeast proteins as well as the sequencing of a novel protein illustrate the potential of the approach. The high data quality in tandem mass spectra and the additional information provided by the isotopic end labeling of peptides enabled automated interpretation of the spectra via simple software algorithms. The technique demonstrated here removes one of the last obstacles to routine and high throughput protein sequencing by mass spectrometry.

  11. Speciation and reactivity of lead and zinc in heavily and poorly contaminated soils: Stable isotope dilution, chemical extraction and model views.

    Science.gov (United States)

    Ren, Zong-Ling; Sivry, Yann; Tharaud, Mickaël; Cordier, Laure; Li, Yongtao; Dai, Jun; Benedetti, Marc F

    2017-06-01

    Correct characterization of metal speciation and reactivity is a prerequisite for the risk assessment and remedial activity management of contaminated soil. To better understand the intrinsic reactivity of Pb and Zn, nine heavily and poorly contaminated soils were investigated using the combined approaches of chemical extractions, multi-element stable isotopic dilution (ID) method, and multi-surface modelling. The ID results show that 0.1-38% of total Pb and 3-45% of total Zn in the studied soils are isotopically exchangeable after a 3-day equilibration. The intercomparison between experimental and modelling results evidences that single extraction with 0.43 M HNO3 solubilizes part of non-isotopically exchangeable fraction of Pb and Zn in the studied soils, and cannot be used as a surrogate for ID to assess labile Pb and Zn pools in soil. Both selective sequential extraction (SSE) and modelling reveal that Mn oxides are the predominant sorption surface for Pb in the studied soils; while Zn is predicted to be mainly associated with soil organic matter in the soil with low pH and Fe/Mn oxides in the soils with high pH. Multi-surface modelling can provide a reasonable prediction of Pb and Zn adsorption onto different soil constituents for the most of the studied soils. The modelling could be a promising tool to decipher the underlying mechanism that controls metal reactivity in soil, but the submodel for Mn oxides should be incorporated and the model parameters, especially for the 2-pK diffuse layer model for Mn oxides, should be updated in the further studies. Copyright © 2017. Published by Elsevier Ltd.

  12. Methods of isotopic geochronology

    Science.gov (United States)

    Gorokhov, I. M.; Levchenkov, O. A.

    Papers are presented on such topics as the age of the chemical elements; the age of meteorites, the moon, and the earth; isotopic ages of the most ancient terrestrial formations; and the Archean evolution of Enderby Land in the Antarctic as evidenced by isotopic dating. Consideration is also given to a uranium-lead geochronology technique for investigating Precambrian ore deposits, a Pb-Pb technique of zircon dating, and the potentials and limitations of Sm-Nd geochronology.

  13. Application of Isotope Dilution Mass Spectrometry for Reference Measurements of Cadmium. Copper, Mercury, Lead, Zinc and Methyl Mercury in Marine Sediment Sample

    Directory of Open Access Journals (Sweden)

    Vasileva E.

    2013-04-01

    Full Text Available Marine sediment was selected as a test sample for the laboratory inter-comparison studies organized by the Environment Laboratoryes of the International Atomic Energy. The analytical procedure to establish the reference values for the Cd, Cu, Hg, Methyl Hg, Pb and Zn amount contents was based on Isotope Dilution Inductively Coupled Plasma-Mass Spectrometry (ID ICP-MS applied as a primary method of measurement..The Hg and Methyl Hg determination will be detailed more specifically because of the problems encountered with this element, including sample homogeneity issues, memory effects and possible matrix effects during the ICP- MS measurement stage. Reference values, traceable to the SI, with total uncertainties of less than 2% relative expanded uncertainty (k=2 were obtained for Cd, Cu, Zn and Pb and around 5% for Hg and CH3Hg.

  14. Isotopes in Greenland Precipitation

    DEFF Research Database (Denmark)

    Faber, Anne-Katrine

    the Arctic Ocean. A comprehensive database is created based on ice core and weather station data from Greenland within the period 1890-2014. Present day annual and seasonal mean values are computed for 326 locations in Greenland. Parameterization of the spatial distribution of temperature and δ18O are used...... of model and data can be used to improve the understanding of climate changes. This is done through analysis of isotope modelling, observations and ice core measurements. This dissertation comprises three projects: (1) Modelling the isotopic response to changes in Arctic sea surface conditions, (2......) Constructing a new Greenland database of observations and present-day ice core measurements, and (3) Performance test of isotope-enabled CAM5 for Greenland. The recent decades of rapid Arctic sea ice decline are used as a basis for an observational-based model experiment using the isotope-enabled CAM model 3...

  15. A method for rapid in situ extraction and laboratory determination of Th, Pb, and Ra isotopes from large volumes of seawater

    Science.gov (United States)

    Baskaran, M.; Murphy, David J.; Santschi, Peter H.; Orr, James C.; Schink, David R.

    1993-04-01

    An in situ pump and six channel extraction system, operating typically at 351 min -1, can not only filter seawater samples but also extract dissolved Th, Pb and Ra isotopes from large volumes of seawater at six different depths on a single lowering. By gamma counting the ash residues of three cartridges (one particle extractor and two nuclide extractors), we can determine 234Th and 210Pb concentrations in the particulate and dissolved phase. Extraction efficiencies for 234Th from the dissolved phase average 93 ± 5% and for 210Pb average ≥90%. At the same time we can determine radium isotopic ratios precisely, but, at present radium concentrations can only be established by the determination of 226Ra in a 30-1 cohort sample. This system can be deployed easily from ships having an A-frame. It eliminates the problems of transporting and processing large volumes of samples and involves relatively little manual labor and analytical time. We have tested and used this device repeatedly in the Gulf of Mexico. Our preliminary results agree well with values of 234Th and 210Pb concentrations and 228Ra/ 226Ra activity ratios reported in the literature for the Gulf of Mexico.

  16. Chromium Isotopes Record Fluctuations in Precambrian Biospheric Oxygenation

    Science.gov (United States)

    Frei, R.; Gaucher, C.; Poulton, S. W.; Canfield, D. E.

    2009-12-01

    There is a direct relationship between life, oxygen, and the surface chemistry of the Earth. Geochemical data suggest that oxygenation of the Earth's atmosphere occurred in two broad steps, near the beginning and the end of the Proterozoic Eon (2500 to 542 million years ago), but the details of this history are unclear. The geochemical behaviour of chromium (Cr) is highly sensitive to the redox state of the surface environment as oxidative weathering processes produce the oxidised hexavalent [Cr(VI)] form. Oxidation of reduced trivaltent [Cr(III)] chromium on land is accompanied by an isotopic fractionation, leading to enrichment of the mobile hexavalent form in the heavier isotope. The fractionated Cr isotope signature is then tranfered by riverine transport to the sea. Here, we use Cr stable isotopes from banded iron formations (BIFs) to track the presence of Cr(VI) in Precambrian oceans, providing a time-resolved picture of the oxygenation history of Earth’s atmosphere-hydrosphere system. Fractionated Cr isotopes indicate the accumulation of Cr(VI) in ocean surface waters ~2.8 to 2.6 billion years (Gyr) ago and a likely transient elevation in atmospheric and surface ocean oxygen prior to the first great rise of oxygen 2.45-2.2 Gyr ago (the Great Oxidation Event; GOE). In contrast, Cr isotopes in ~1.88 Gyr old BIFs are not fractionated, indicating a major decline in atmospheric oxygen and demonstrating that the GOE did not lead to a unidirectional stepwise increase in atmospheric oxygen. In the late Neoproterozoic, ~800 to 542 million years (Myr) ago, we observe strong positive fractionations in Cr isotopes (δ53Cr up to +4.9 ‰) providing independent support for increased surface oxygenation at this time. This may have stimulated rapid evolution of macroscopic multicellular life. Our chromium isotope data thus provide new insights into the oxygenation history of the Earth, and highlight its use as a powerful redox tracer in aquatic systems.

  17. 铅同位素比率分析技术在食品污染源解析中的应用%APPLICATIONS OF LEAD ISOTOPE RATIOS FOR IDENTIFICATION AND APPORTIONMENT ON POLLUTION SOURCES IN FOOD

    Institute of Scientific and Technical Information of China (English)

    赵多勇; 魏益民; 郭波莉; 魏帅

    2011-01-01

    铅是一种有毒有害重金属,可通过膳食、呼吸等途径进入人体,并蓄积达到有害水平.由于食用农产品产地环境不断受到铅的污染,使得"从农田到餐桌"食品供应链在最初环节存在较大的风险,因此土壤、大气等环境介质成为食品铅污染的可能来源.为准确找到污染源并及时切断污染途径,降低危害发生的概率,追溯食品中铅污染物的来源显得尤为重要.铅同位素比率分析技术是追溯铅来源的一种有效方法,该方法结合相应模型可推测食品铅污染的来源及各污染源的相对贡献率.本文阐述了食品中铅污染物的来源,铅同位素比率分析技术溯源的原理、方法,以及该方法在蔬菜、茶叶、葡萄酒、谷物等食品铅污染物溯源中的应用现状,旨在为食品铅污染溯源和控制提供理论和技术参考.%Lead is one of the toxic heavy metals which can accumulate to an adverse effect level in human bodies through ingestion, inhalation or other pathways. Because of the persistent lead contamination in farmland environment, large risk exists in the primary stage of "from farm to table" chain. Environmental media such as soils, atmospheric aerosols were the possible lead sources of agro-food. To prinpoint the pollution sources exactly, cut off the contamination pathways in time, and reduce the risk of hazard, pollution sources tracing was very important. Lead isotope ratio combined with certain models is an effective method to, discriminate correctly the pollution sources and calculate the individual source contributions. In this review, to provide theoretical and technical reference for controlling lead pollution in environment and food, lead pollution sources in food, tracing principle and methods of lead isotope ratios, and its applications on vegetable, tea, wine, cereal and other food products were concerned.

  18. Rapid crystal recycling at Krafla Volcano, Iceland, inferred from oxygen-isotope and trace- element compositions and U-Th-Ra disequilibria in plagioclase

    Science.gov (United States)

    Cooper, K. M.; Sims, K. W.; Eiler, J. M.; Banerjee, N. R.

    2008-12-01

    The Icelandic central volcano of Krafla exhibits increasing assimilation of hydrothermally-altered crust with increasing differentiation of magmas, as evidenced by decreasing δ18O with decreasing MgO (Nicholson et al., 1991, J Pet 32, p.1005). The Krafla Fires eruption (1975-84) produced two different magma compositions simultaneously: quartz tholeiites near the center of the volcano, and olivine tholeiites north of the central volcano (Gronvold et al., 2008, Goldschmidt abstract). Examination of crystals in these magmas has the potential to provide information about the nature and timescales of mixing of distinct magmas and assimilation of crustal material at Krafla. We present oxygen-isotope compositions, trace-element compositions, and 238U-230Th-226Ra disequilibria measured in plagioclase crystals from samples of lavas erupted during two phases of the Krafla Fires eruption (ol tholeiite erupted Jan-Feb 1981, and qz tholeiite erupted Nov 1981). Oxygen-isotope data for multiple size fractions of plagioclase show a decrease in δ18O with increasing crystal size for the ol tholeiite (from ~4.1 permil to 3.5 permil), whereas there is no clear relationship between plagioclase size and oxygen-isotope composition in the qtz tholeiite (all size fractions average 4.1-4.3 permil). Furthermore, all measured plagioclase have δ18O lower than would be in equilibrium with the whole rock measurements (by up to 1.5 permil). These data imply that (1) few or none of the measured crystals precipitated from the host liquids, and (2) the crystals were entrained in the host magmas shortly prior to eruption, allowing them to maintain oxygen isotopic disequilibrium and heterogeneity within the crystal populations. These inferences are corroborated by trace element compositions measured in plagioclase by laser-ablation ICPMS, as the majority of analyzed points have Ba and Sr concentrations inconsistent with equilibrium partitioning between crystals and liquid. Furthermore, in the case

  19. Lithium isotope separation by laser

    Energy Technology Data Exchange (ETDEWEB)

    Arisawa, T.; Maruyama, Y.; Suzuki, Y.; Shiba, K.

    1982-01-01

    A lithium isotope separation was performed using a laser isotope separation method. It was found that the lithium atoms with a natural isotopic abundance enhanced its /sup 6/Li concentration up to over 90% by tuning the laser wavelength to the /sup 2/Psub(1/2) of /sup 6/Li. Too high power, however, leads to a loss of enrichment due to the power broadening effect which was analysed by the equation of motion of density matrices.

  20. Stable isotope probing and dynamic loading experiments provide insight into the ecophysiology of novel ammonia oxidizers in rapid gravity sand filters

    OpenAIRE

    Fowler, Jane; Palomo, Alejandro; Gülay, Arda; Tatari, Karolina; Thamdrup, Bo; Albrechtsen, Hans-Jørgen; Sørensen, Søren; Barth F. Smets

    2016-01-01

    Nitrification is often the dominant microbial process in rapid gravity sand filters (RSF), used to treat aerated groundwater to produce drinking water. RSFs harbor diverse microbial communities including a range of ammonia oxidizing clades; Betaproteobacteria (Nitrosomonas, Nitrosospira), Archaea, diverse potentially ammonia oxidizing heterotrophs and abundant Nitrospira spp., recently shown to comprise both canonical nitrite oxidizing as well as complete ammonium oxidizing (comammox) types. ...

  1. Rapid Environmental Fluctuations Recorded over the Last Glacial/Interglacial Cycle in the Sediments from Borehole PRGL1-4 (Gulf of Lions; Western Mediterranean) using Radiogenic Isotopes (Sr & Nd)

    Science.gov (United States)

    Nizou, J.

    2015-12-01

    The study of sediments deposited and preserved in oceanic basins unable us to examine how terrigenous sediment supply varied through time in relation to paleoenvironmental and climatic changes on land. The geochemical and isotopic compositions of marine sediment are used to unravel its provenance, and provide information about its formation. Providing that the paleoclimatic frame is known, such data give an insight into the rock-source location and allow us to decipher between genetic processes of mechanical erosion and chemical alteration. Borehole PRGL1-4 (European project PROMESS), located in the Gulf of Lions (W Mediterranean) at 300 mwd, was investigated geochemically at high-temporal resolution over the last glacial/interglacial cycle (i.e. 130 ka) to study sediment-source variations during rapid climate changes. Besides, sediments originating from the Rhône's and the Pyreneo-Languedocian's catchment areas have been analyzed to measure the isotopic composition of five source end-members that are the Alps, the Higher Rhône valley, the Lower Rhône valley, the Languedoc and the Pyrenees. Epsilon Nd and 87Sr/86Sr were measured on 60 samples encompassing 4 marine isotopic stages with an emphasis on Heinrich events. The epsilon Nd values of PRGL1-4 lean towards the Lower Rhône valley unradiogenic end-member during cold stadial intervals, and towards the Alpine radiogenic end-member during warm interstadials. The presence of an ice cap over the crystalline Alpine watershed during cold phases could prevent the sediments originating from this region from reaching the Gulf of Lions. The same pattern is observed during the time of Heinrich events. An influence of the sea level variations on the sedimentation at the borehole site during the Heinrich events is unlikely since they are only 10 to 15 m in amplitude. Furthermore, a major isotopic shift in epsilon Nd mean values is displayed around 40 ka that coincides with the connection of the Durance to the Rhône River

  2. Isotopically controlled semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Haller, E.E.

    2004-11-15

    A review of recent research involving isotopically controlled semiconductors is presented. Studies with isotopically enriched semiconductor structures experienced a dramatic expansion at the end of the Cold War when significant quantities of enriched isotopes of elements forming semiconductors became available for worldwide collaborations. Isotopes of an element differ in nuclear mass, may have different nuclear spins and undergo different nuclear reactions. Among the latter, the capture of thermal neutrons which can lead to neutron transmutation doping, can be considered the most important one for semiconductors. Experimental and theoretical research exploiting the differences in all the properties has been conducted and will be illustrated with selected examples. Manuel Cardona, the longtime editor-in-chief of Solid State Communications has been and continues to be one of the major contributors to this field of solid state physics and it is a great pleasure to dedicate this review to him.

  3. Two series of copper-gold deposits in the middle and lower reaches of the Yangtze River area (MLYRA) and the hydrogen, oxygen, sulfur and lead isotopes of their ore-forming hydrothermal systems

    Institute of Scientific and Technical Information of China (English)

    周涛发; 袁峰; 岳书仓; 赵勇

    2000-01-01

    Based on studies on the geological characteristics of the copper-gold deposits in the middle and lower reaches of the Yangtze River area (MLYRA) and their hydrogen, oxygen, sulfur and lead isotope compositions, it is concluded that there existed two series of copper-gold deposits. They are evolutional products of two ore-forming hydrothermal systems in different geodynamic settings and geological era. Series I is stratiform or stratabound copper-gold deposits. These deposits were formed by submarine exhalation and sedimentation of hydrothermal solutions in Her-cynian tensional tectonic environment after bot brine ascending along contemporaneous faults and exhaled into the sea-floor. Series II consists of copper-gold deposits related to medium and acidic magmatic intrusions. Their mineralizations took place in Yanshanian in a tensional or a transitional period to the tensional tectonic environment from the composite of the tethys tectonic regime and the Paleo-Pacific ocean tectonic regime, as well as in

  4. Fluctuations in Precambrian atmospheric oxygenation recorded by chromium isotopes

    Science.gov (United States)

    Frei, Robert; Gaucher, Claudio; Poulton, Simon W.; Canfield, Don E.

    2009-09-01

    Geochemical data suggest that oxygenation of the Earth's atmosphere occurred in two broad steps. The first rise in atmospheric oxygen is thought to have occurred between ~2.45 and 2.2Gyr ago, leading to a significant increase in atmospheric oxygen concentrations and concomitant oxygenation of the shallow surface ocean. The second increase in atmospheric oxygen appears to have taken place in distinct stages during the late Neoproterozoic era (~800-542Myr ago), ultimately leading to oxygenation of the deep ocean ~580Myr ago, but details of the evolution of atmospheric oxygenation remain uncertain. Here we use chromium (Cr) stable isotopes from banded iron formations (BIFs) to track the presence of Cr(VI) in Precambrian oceans, providing a time-resolved picture of the oxygenation history of the Earth's atmosphere-hydrosphere system. The geochemical behaviour of Cr is highly sensitive to the redox state of the surface environment because oxidative weathering processes produce the oxidized hexavalent [Cr(VI)] form. Oxidation of reduced trivalent [Cr(III)] chromium on land is accompanied by an isotopic fractionation, leading to enrichment of the mobile hexavalent form in the heavier isotope. Our fractionated Cr isotope data indicate the accumulation of Cr(VI) in ocean surface waters ~2.8 to 2.6Gyr ago and a likely transient elevation in atmospheric and surface ocean oxygenation before the first great rise of oxygen 2.45-2.2Gyr ago (the Great Oxidation Event). In ~1.88-Gyr-old BIFs we find that Cr isotopes are not fractionated, indicating a decline in atmospheric oxygen. Our findings suggest that the Great Oxidation Event did not lead to a unidirectional stepwise increase in atmospheric oxygen. In the late Neoproterozoic, we observe strong positive fractionations in Cr isotopes (δ53Cr up to +4.9‰), providing independent support for increased surface oxygenation at that time, which may have stimulated rapid evolution of macroscopic multicellular life.

  5. Monte Carlo calculations on transmutation of trans-uranic nuclear waste isotopes using spallation neutrons difference of lead and graphite moderators

    CERN Document Server

    Hashemi-Nezhad, S R; Brandt, R; Krivopustov, M I; Kulakov, B A; Odoj, R; Sosnin, A N; Wan, J S; Westmeier, W

    2002-01-01

    Transmutation rates of sup 2 sup 3 sup 9 Pu and some minor actinides ( sup 2 sup 3 sup 7 Np, sup 2 sup 4 sup 1 Am, sup 2 sup 4 sup 5 Cm and sup 2 sup 4 sup 6 Cm), in two accelerator-driven systems (ADS) with lead or graphite moderating environments, were calculated using the LAHET code system. The ADS that were used had a large volume (approx 32 m sup 3) and contained no fissile material, except for a small amount of fissionable waste nuclei that existed in some cases. Calculations were performed at an incident proton energy of 1.5 GeV and the spallation target was lead. Also breeding rates of sup 2 sup 3 sup 9 Pu and sup 2 sup 3 sup 3 U as well as the transmutation rates of two long-lived fission products sup 9 sup 9 Tc and sup 1 sup 2 sup 9 I were calculated at different locations in the moderator. It is shown that an ADS with graphite moderator is a much more effective transmuter than that with lead moderator.

  6. A Record of the Eastern Tropical Pacific of Water Column Structure Reorganization during the Rapid Climate Changes of Marine Isotope Stage 3.

    Science.gov (United States)

    Hendy, I. L.

    2007-05-01

    Little is known about the details of paleoceanographic changes in the Eastern Tropical Pacific (ETP) during marine isotope stage 3. Here we present a high resolution record of climate change from core ME0005A 10JC (15.7°N; 95.3°E, 1040 m water depth) collected in the Gulf of Tehuantepec spanning 48 to 38 Ka. Planktonic and benthic stable isotope records have been generated alongside Corg, carbonate, δ15N and trace metal concentrations of bulk sediments. Seasonal intense wind forced upwelling produces high Corg flux in the Gulf. In winter, high atmospheric pressures in the Gulf of Mexico and low pressures in the ETP (associated with the ITCZ) create a strong pressure gradient generally blocked by high mountains along the isthmus. A gap near the Gulf of Tehuantepec allows air to spill over into the Pacific creating a hurricane force wind (the Tehuanos) that pushes water off the broad shelf, producing non-Ekman upwelling. Corg production increases from 48 to 38 Ka in association with increasing nitrate utilization as indicated by increasing δ15N values. Conservative trace metals increase relative to non-conservative between 45 and 43 Ka simultaneously with shift to more positive benthic δ13C, while non-conservative (nutrient- like) metals increase after 43 Ka. A prominent short ~1‰ negative shift in benthic δ18O occurs at 44.5 Ka with a 0.5‰ positive step occurring at 43.5 Ka. Globigerina ruber records δ18O values of ~-1‰ between 46 and 45 Ka, decreasing by ~1‰ at 45 Ka, while δ13C values vary between 0 and 1‰. Globigerina bulloides records δ18O values of ~0.5‰ and δ13C of 1‰ between 46 and 45 Ka, but records δ18O values of ~-1‰ and δ13C of -1‰ between 44 and 42 Ka. G. bulloides is associated with winter upwelling in the region, while G. ruber is a surface dweller associated with the Costa Rica Current that enters the Gulf in summer. Neogloboquadrina dutertrei and Globorotalia menardii generally record δ18O values of 0.5 to 0‰ and δ13

  7. Carbon isotopic composition of branched tetraether membrane lipids in soils suggest a rapid turnover and a heterotrophic life style of their source organism(s

    Directory of Open Access Journals (Sweden)

    J. W. H. Weijers

    2010-09-01

    Full Text Available Branched Glycerol Dialkyl Glycerol Tetraethers (GDGTs are membrane spanning lipids synthesised by as yet unknown bacteria that thrive in soils and peat. In order to obtain more information on their ecological niche, the stable carbon isotopic composition of branched GDGT-derived alkanes, obtained upon ether bond cleavage, has been determined in a peat and various soils, i.e. forest, grassland and cropland, covered by various vegetation types, i.e., C3- vs. C4-plant type. These δ13C values are compared with those of bulk organic matter and higher plant derived n-alkanes from the same soils. With average δ13C values of −28‰, branched GDGTs in C3 soils are only slightly depleted (ca. 1‰ relative to bulk organic carbon and on average 8.5‰ enriched relative to plant wax-derived long-chain n-alkanes ( nC29nC33. In an Australian soil dominantly covered with C4 type vegetation, the branched GDGTs have a δ13C value of −18‰, clearly higher than observed in soils with C3 type vegetation. As with C3 vegetated soils, branched GDGT δ13C values are slightly depleted (1‰ relative to bulk organic carbon and enriched (ca. 5‰ relative to n-alkanes in this soil. The δ13C values of branched GDGT lipids being similar to bulk organic carbon and their co-variation with those of bulk organic carbon and plant waxes, suggest a heterotrophic life style and assimilation of relatively heavy and likely labile substrates for the as yet unknown soil bacteria that synthesise the branched GDGT lipids. However, a chemoautotrophic lifestyle, i.e. consuming respired CO2, could not be fully excluded based on these data alone. Based on a natural labelling experiment of a C3/C4 crop change introduced on one of the soils 23 years before sampling and based

  8. Genome sequence of E. coli O104:H4 leads to rapid development of a targeted antimicrobial agent against this emerging pathogen.

    Science.gov (United States)

    A recent widespread outbreak of Escherichia coli O104:H4 in Germany demonstrates the dynamic nature of emerging and re-emerging food-borne pathogens, particularly STECs and related pathogenic E. coli. Rapid genomic sequencing and public availability of these data from the German outbreak strain allo...

  9. Spatial distribution, health risk assessment, and isotopic composition of lead contamination of street dusts in different functional areas of Beijing, China.

    Science.gov (United States)

    Han, Lanfang; Gao, Bo; Wei, Xin; Xu, Dongyu; Gao, Li

    2016-02-01

    Street dusts from heavy density traffic area (HDTA), tourism area (TA), residential area (RA), and educational area (EA) in Beijing were collected to explore the distribution, health risk assessment, and source of lead (Pb). The average concentration of Pb in TA was the highest among the four areas. Compared with other cities, Pb concentrations in Beijing were generally at moderate or low levels. The average value (14.05) of ecological risk index (RI) indicated that Pb was at "low pollution risk" status. According to the calculation on hazard index (HI), the ingestion of dust particles of children and adults was the major route of exposure to street dusts in four studied areas, followed by dermal contact. The lower values of HI than 1 further suggested that non-carcinogenic risks of Pb in the street dusts were in the low range. Comparing (206)Pb/(207)Pb and (208)Pb/(207)Pb ratios of street dusts with other environmental samples, it was found that atmospheric deposition of coal combustion dust might be the main pathway for anthropogenic Pb input to the street dusts in four functional areas.

  10. Shear heating and clumped isotope reordering in carbonate faults

    Science.gov (United States)

    Siman-Tov, Shalev; Affek, Hagit P.; Matthews, Alan; Aharonov, Einat; Reches, Ze'ev

    2016-07-01

    Natural faults are expected to heat rapidly during seismic slip and to cool quite quickly after the slip event. Here we examine clumped isotope thermometry for its ability to identify such short duration elevated temperature events along frictionally heated carbonate faults. Our approach is based on measured Δ47 values that reflect the distribution of oxygen and carbon isotopes in the calcite lattice, measuring the abundance of 13Csbnd 18O bonds, which is affected by temperature. We examine three types of calcite rock samples: (1) crushed limestone grains that were rapidly heated and then cooled in static laboratory experiments, simulating the temperature cycle experienced by fault rock during an earthquake slip; (2) limestone samples that were experimentally sheared to simulate earthquake slip events; and (3) samples from Fault Mirrors (FMs) collected from principle slip surfaces of three natural carbonate faults. Extensive FM surfaces are believed to form during earthquake slip. Our experimental results show that Δ47 values decrease rapidly (in the course of seconds) with increasing temperature and shear velocity. On the other hand, carbonate shear zones from natural faults do not show such Δ47 decrease. We suggest that the Δ47 response may be controlled by nano-size grains, the high abundance of defects, and highly stressed/strained grain boundaries within the carbonate fault zone that can reduce the activation energy for diffusion, and thus lead to an increased rate of isotopic disordering during shear experiments. In our laboratory experiments the high stress and strain on grain contacts and the presence of nanograins thus allows for rapid disordering so that a change in Δ47 occurs in a very short and relatively low intensity heating events. In natural faults it may also lead to isotopic ordering after the cessation of frictional heating thus erasing the high temperature signature of Δ47.

  11. Preliminary studies leading to a conceptual design of a 1000 MWe fast neutron reactor; Etudes preliminaires conduisant a un concept de reacteur a neutrons rapides de 1000 MWe

    Energy Technology Data Exchange (ETDEWEB)

    Vendryes, G.; Zaleski, C.P. [Association Euratom-CEA Cadarache (France). Centre d' Etudes Nucleaires

    1964-07-01

    This report presents the results of studies which seemed important to undertake in connexion with the development of fast neutron reactors. - It points out the advantage of high internal breeding ratios ({approx}1, 1) which are necessary in order to get a small change in time both in power distribution and reactivity (less: than 0.005 {delta}k/k in 18 months). - It shows how to achieve this goal, when simultaneously power distribution flattening is obtained. These results in a higher mean specific power (which is an economic gain) and therefore in a smaller doubling time (about 10 years). - It attempts to find criteria concerning the specific power that should be used in future reactor designs -It presents a conceptional design of a 1000 MWe fast neutron reactor, for the realisation of which no technological impossibility appears. - It shows that the dynamic behaviour seems satisfactory despite a positive total isothermal sodium coefficient. - It tries to predict the development of fast reactors within the future total nuclear program. It does not appear that fissile materials supply problems should in France slow down the development of fast neutron reactors, which will be essentially tied up to its economical ability to produce cheap electric power. (authors) [French] Ce rapport presente les etudes qu'il nous a paru important d'aborder dans le cadre du developpement des reacteurs a neutrons rapides. - Il met en evidence l'interet des taux de regeneration internes eleves ({approx}1, 1) pour obtenir une bonne evolution dans le temps de la distribution de puissance et de la reactivite (moins de 0,005 {delta}k/k pour 18 mois). - Il montre la possibilite d'y parvenir tout en applatissant la distribution des fissions, ce qui se traduit par une puissance specifique moyenne plus elevee (gain economique), et donc un temps de doublement plus faible de l'ordte de 10 ans - Il tente de definir un optimum de la puissance specifique valable pour les

  12. Exposure of barley plants to low Pi leads to rapid changes in root respiration that correlate with specific alterations in amino acid substrates.

    Science.gov (United States)

    Alexova, Ralitza; Nelson, Clark J; Jacoby, Richard P; Millar, A Harvey

    2015-04-01

    The majority of inorganic phosphate (Pi ) stress studies in plants have focused on the response after growth has been retarded. Evidence from transcript analysis, however, shows that a Pi -stress specific response is initiated within minutes of transfer to low Pi and in crop plants precedes the expression of Pi transporters and depletion of vacuolar Pi reserves by days. In order to investigate the physiological and metabolic events during early exposure to low Pi in grain crops, we monitored the response of whole barley plants during the first hours following Pi withdrawal. Lowering the concentration of Pi led to rapid changes in root respiration and leaf gas exchange throughout the early phase of the light course. Combining amino and organic acid analysis with (15) N labelling we show a root-specific effect on nitrogen metabolism linked to specific substrates of respiration as soon as 1 h following Pi withdrawal; this explains the respiratory responses observed and was confirmed by stimulation of respiration by exogenous addition of these respiratory substrates to roots. The rapid adjustment of substrates for respiration in roots during short-term Pi -stress is highlighted and this could help guide roots towards Pi -rich soil patches without compromising biomass accumulation of the plant. © 2014 The Authors. New Phytologist © 2014 New Phytologist Trust.

  13. Oxygen Isotopes in Meteorites

    Science.gov (United States)

    Clayton, R. N.

    2003-12-01

    wavelength range 90-100 nm. The reaction proceeds by a predissociation mechanism, in which the excited electronic state lives long enough to have well-defined vibrational and rotational energy levels. As a consequence, the three isotopic species - C16O, C17O, and C18O - absorb at different wavelengths, corresponding to the isotope shift in vibrational frequencies. Because of their different number densities, the abundant C16O becomes optically thick in the outermost part of the cloud (nearest to the external source of UV radiation), while the rare C17O and C18O remain optically thin, and hence dissociate at a greater rate in the cloud interior. The differences in chemical reactivity between C16O molecules and 17O and 18O atoms may lead to isotopically selective reaction products. This scenario has been suggested to explain meteoritic isotope patterns, as discussed below (Yurimoto and Kuramoto, 2002).Stable isotope abundances in meteoritic material provide an opportunity to evaluate the thoroughness of mixing of isotopes of diverse stellar sources. Molybdenum presents a good test case: it has seven stable isotopes, derived from at least three types of stellar sources, corresponding to the r-process, s-process, and p-process. Presolar silicon carbide grains, extracted from primitive meteorites, contain molybdenum that has been subject to s-process neutron capture in red-giant stars, resulting in large enrichments of isotopes at masses 95, 96, 97, 98, and severe depletions (up to 100%) of isotopes at masses 92 and 94 (p-process) and 100 (r-process) (Nicolussi et al., 1998). Complementary patterns have been found in whole-rock samples of several meteorites, with >1,000-fold smaller amplitude, suggesting the preservation of a small fraction of the initial isotopic heterogeneity ( Yin et al., 2002; Dauphas et al., 2002). Oxygen is another element for which primordial isotopic heterogeneity might be preserved. This is discussed further below.It would be highly desirable to have

  14. Leatherback Isotopes

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — SWFSC is currently working on a project identifying global marine isotopes using leatherback turtles (Dermochelys coriacea) as the indicator species. We currently...

  15. Isotopic chirality

    Energy Technology Data Exchange (ETDEWEB)

    Floss, H.G. [Univ. of Washington, Seattle, WA (United States)

    1994-12-01

    This paper deals with compounds that are chiral-at least in part, due to isotope substitution-and their use in tracing the steric course of enzyme reaction in vitro and in vivo. There are other applications of isotopically chiral compounds (for example, in analyzing the steric course of nonenzymatic reactions and in probing the conformation of biomolecules) that are important but they will not be discussed in this context.

  16. Isotopic Paleoclimatology

    Science.gov (United States)

    Bowen, R.

    Paleotemperature scales were calculated by H. C. Urey and others in the 1950s to assess past temperatures, and later work using the stable isotopes of oxygen, hydrogen, and carbon employed standards such as Peedee belemnite (PDB) and Standard Mean Ocean Water (SMOW). Subsequently, subjects as diverse as ice volume and paleotemperatures, oceanic ice and sediment cores, Pleistocene/Holocene climatic changes, and isotope chronostratigraphy extending back to the Precambrian were investigated.

  17. Barriers on the Brink? Interactions Between Biological and Physical Processes Lead to Bistability and the Potential for Rapid Response to Gradually Changing Conditions (Invited)

    Science.gov (United States)

    Moore, L. J.; Duran Vinent, O.

    2013-12-01

    Barrier islands and their habitats are especially sensitive to changing environmental conditions. As sea level rises, storm intensity increases and plant species composition changes, interactions among biological and physical processes will play a critical role in determining how barrier islands will evolve. Within a new conceptual framework, islands tend to exist in one of two primary states. 'Low-elevation' islands have little relief above sea level and are dominated by external processes, responding quickly on short time scales to changes in forcing (e.g., storms, sea level rise, etc.), migrating rapidly and generally being low in ecological diversity and productivity. In contrast, 'high-elevation' islands are less vulnerable to storms, tend to be dominated by internal processes (e.g., sand trapping by vegetation), require long time periods to respond to changes in forcing, migrate slowly (if at all) and host a range of plant species and morphological environments including shrubs, small trees and vegetated secondary and tertiary dunes with intervening swales. The continued existence of barrier island landforms will depend on the degree to which islands can maintain elevation above sea level while also responding to changes in forcing by migrating landward. Using a new model that simulates the co-evolution of island topography and vegetation, we demonstrate that barrier islands can undergo rapid deterioration in response to gradual changes in forcing. Model simulations indicate that once the ratio between the time required for island vegetation to re-establish after a storm and the time between storms becomes greater than 1, barrier islands become bistable. Simulations and observations indicate that once islands enter this regime, strong storms can trigger a shift from a high-elevation state (resistant to storms) to a low-elevation state (prone to storm overwash). At this point, the probability of returning to the high-elevation state decreases exponentially as

  18. INVESTIGATION OF ADSORPTION, DISTRIBUTION AND MIGRATION OF LEAD BETWEEN ENVIRONMENT AND PLANT BY STABLE LEAD ISOTOPIC TRACER%铅在植物-环境体系中的吸收、分布和迁移规律的稳定同位素示踪法研究

    Institute of Scientific and Technical Information of China (English)

    黄华斌; 庄峙厦; 杨妙峰; 张建平; 齐士林; 罗洁; 王小如

    2009-01-01

    Low concentration isotopic lead tracer (SRM982) was adopted, ICP-MS was used as a detection tool. By pot test, the chemical action of lead in tea under the condition of different pH and different modes of lead exposure was studied. Simulated rain water (C_(pb) = 0.5mg·l~(-1)) was used to pot soil and spray leaf to investigate the adsorption, distribution and migration of lead in two systerms: atmosphere-tea and soil-tea. The results are: 1. the reaction to lead pollution from atmosphere is more sensitive than that from soil; 2. the migration and distribution in tea of lead pollution from atmosphere and from soil is different, the former has the trend of conveying to bud while the latter focus mainly in root; 3. pH has an evidently effect on the migration of lead in tea, generally, low pH facilitates migration to upper parts. This method has the advantages that tea beared low polution, and the hazard to plant is less than traditional ways. In addition, lead from environment and from tracer can be separated.%以低浓度的稳定铅同位素为示踪剂,采用电感耦合等离子质谱法,通过盆栽实验,考察了在不同的pH值环境和不同铅源引入方式下,茶树植株对铅的吸收情况以及铅在植株体内的分布及迁移规律.结果表明:茶树植株对大气铅源污染的反应比土壤铅源污染灵敏;大气铅源污染有往顶端(芽)迁移的趋势,而土壤铅源污染则主要聚集在根部;低pH条件增强植株对铅的吸收且能促使植株体内的铅的往高处迁移.本实验方法危害小,更接近植株承受低浓度污染的实际情况,能区分实验引入铅源和环境引入铅源.

  19. 原子吸收法快速测定石脑油中微量铅%Rapid determination of trace lead content in naphtha

    Institute of Scientific and Technical Information of China (English)

    赵文锐; 倪前龙

    2014-01-01

    Determination of lead content in naphtha by direct injection graphite furnace atomic absorp‐tion spectroscopy was studied with ethanol as solvent ,palladium nitrate as matrix modifiers .The test re‐sults indicated that it w as satisfied in the lead content range of 0‐100μg/L ,the linearly dependent coeffi‐cient w as 0.999317 ,the recovery ratio w as 94.6%‐105.1% .%将试样用无水乙醇溶液稀释,以硝酸钯为基体改性剂,用石墨炉原子吸收光谱法直接进样,测定石脑油中的微量铅含量。实验表明,铅质量浓度在0~100μg/L范围内,线性关系良好,相关系数为0.999317,回收率为94.6%~105.1%。

  20. Repeated sensory contact with aggressive mice rapidly leads to an anticipatory increase in core body temperature and physical activity that precedes the onset of aversive responding.

    Science.gov (United States)

    Pardon, Marie-Christine; Kendall, David A; Pérez-Diaz, Fernando; Duxon, Mark S; Marsden, Charles A

    2004-08-01

    The present study investigated whether the 'psychological threat' induced by sensory contact with an aggressive conspecific would be a sufficient factor in inducing behavioural and physiological disturbances. Repeated sensory contact with an aggressive mouse (social threat) in a partitioned cage was compared with repeated exposure to a novel partitioned cage in male NMRI mice. We first examined parameters of stress responsiveness (body weight, plasma corticosterone levels, frequency of self-grooming and defecation). The temperature and physical activity responses to stress were also recorded during and after the 4 weeks of stress using radiotelemetry. Finally, cognitivo-emotional performance was assessed after acute stress and 2 and 4 weeks of stress by measuring decision making, sequential alternation performance and behaviour in the elevated T-maze. Social threat had a greater impact than novel cage exposure on most parameters of stress responsiveness, although mice did not habituate to either stressor. Social threat rapidly led to an anticipatory rise in core body temperature and physical activity before the scheduled stress sessions. Such anticipation developed within the first week and persisted for 9 days after ending the stress procedure. Some memory impairment in the sequential alternation test was found in stressed mice, independent of the stressor. After 4 weeks of stress, inhibitory avoidance in the elevated T-maze was enhanced in socially stressed mice and reduced in novel cage mice. The sustained anticipation of stress in the social threat group preceded aversive responding. It remains to be established whether anticipation contributes to the development of aversive responses.

  1. Sublethal Ciprofloxacin Treatment Leads to Rapid Development of High-Level Ciprofloxacin Resistance during Long-Term Experimental Evolution of Pseudomonas aeruginosa

    Science.gov (United States)

    Jørgensen, Karin Meinike; Wassermann, Tina; Jensen, Peter Østrup; Hengzuang, Wang; Molin, Søren; Høiby, Niels

    2013-01-01

    The dynamics of occurrence and the genetic basis of ciprofloxacin resistance were studied in a long-term evolution experiment (940 generations) in wild-type, reference strain (PAO1) and hypermutable (PAOΔmutS and PAOMY-Mgm) P. aeruginosa populations continuously exposed to sub-MICs (1/4) of ciprofloxacin. A rapid occurrence of ciprofloxacin-resistant mutants (MIC of ≥12 μg/ml, representing 100 times the MIC of the original population) were observed in all ciprofloxacin-exposed lineages of PAOΔmutS and PAOMY-Mgm populations after 100 and 170 generations, respectively, and in one of the PAO1 lineages after 240 generations. The genetic basis of resistance was mutations in gyrA (C248T and G259T) and gyrB (C1397A). Cross-resistance to beta-lactam antibiotics was observed in the bacterial populations that evolved during exposure to sublethal concentrations of ciprofloxacin. Our study shows that mutants with high-level ciprofloxacin resistance are selected in P. aeruginosa bacterial populations exposed to sub-MICs of ciprofloxacin. This can have implications for the long-term persistence of resistant bacteria and spread of antibiotic resistance by exposure of commensal bacterial flora to low antibiotic concentrations. PMID:23774442

  2. Reduced skeletal muscle mitochondrial respiration and improved glucose metabolism in nondiabetic obese women during a very low calorie dietary intervention leading to rapid weight loss

    DEFF Research Database (Denmark)

    Rabøl, Rasmus; Svendsen, Pernille F; Skovbro, Mette

    2009-01-01

    Reduced oxidative capacity of skeletal muscle has been proposed to lead to accumulation of intramyocellular triglyceride (IMTG) and insulin resistance. We have measured mitochondrial respiration before and after a 10% low-calorie-induced weight loss in young obese women to examine the relationship...... between mitochondrial function, IMTG, and insulin resistance. Nine obese women (age, 32.3 years [SD, 3.0]; body mass index, 33.4 kg/m(2) [SD, 2.6]) completed a 53-day (SE, 3.8) very low calorie diet (VLCD) of 500 to 600 kcal/d without altering physical activity. The target of the intervention was a 10.......79 (SE, 0.02) (P calorie diet; but mitochondrial function decreased, and IMTG remained unchanged. Our results do not support a direct relationship between mitochondrial function and insulin...

  3. Messenger RNA electroporation of human monocytes, followed by rapid in vitro differentiation, leads to highly stimulatory antigen-loaded mature dendritic cells.

    Science.gov (United States)

    Ponsaerts, Peter; Van den Bosch, Glenn; Cools, Nathalie; Van Driessche, Ann; Nijs, Griet; Lenjou, Marc; Lardon, Filip; Van Broeckhoven, Christine; Van Bockstaele, Dirk R; Berneman, Zwi N; Van Tendeloo, Viggo F I

    2002-08-15

    Dendritic cells (DC) are professional Ag-capturing and -presenting cells of the immune system. Because of their exceptional capability of activating tumor-specific T cells, cancer vaccination research is now shifting toward the formulation of a clinical human DC vaccine. We developed a short term and serum-free culture protocol for rapid generation of fully mature, viable, and highly stimulatory CD83(+) DC. Human monocytes were cultured for 24 h in serum-free AIM-V medium, followed by 24-h maturation by polyriboinosinic polyribocytidylic acid (polyI:C). Short term cultured, polyI:C-maturated DC, far more than immature DC, showed typical mature DC markers and high allogeneic stimulatory capacity and had high autologous stimulatory capacity in an influenza model system using peptide-pulsed DC. Electroporation of mRNA as an Ag-loading strategy in these cells was optimized using mRNA encoding the enhanced green fluorescent protein (EGFP). Monocytes electroporated with EGFP mRNA, followed by short term, serum-free differentiation to mature DC, had a phenotype of DC, and all showed positive EGFP fluorescence. Influenza matrix protein mRNA-electroporated monocytes cultured serum-free and maturated with polyI:C showed high stimulatory capacity in autologous T cell activation experiments. In conclusion, the present short term and serum-free ex vivo DC culture protocol in combination with mRNA electroporation at the monocyte stage imply an important reduction in time and consumables for preparation of Ag-loaded mature DC compared with classical DC culture protocols and might find application in clinical immunotherapy settings.

  4. Doxorubicin in vivo rapidly alters expression and translation of myocardial electron transport chain genes, leads to ATP loss and caspase 3 activation.

    Directory of Open Access Journals (Sweden)

    Amy V Pointon

    Full Text Available BACKGROUND: Doxorubicin is one of the most effective anti-cancer drugs but its use is limited by cumulative cardiotoxicity that restricts lifetime dose. Redox damage is one of the most accepted mechanisms of toxicity, but not fully substantiated. Moreover doxorubicin is not an efficient redox cycling compound due to its low redox potential. Here we used genomic and chemical systems approaches in vivo to investigate the mechanisms of doxorubicin cardiotoxicity, and specifically test the hypothesis of redox cycling mediated cardiotoxicity. METHODOLOGY/PRINCIPAL FINDINGS: Mice were treated with an acute dose of either doxorubicin (DOX (15 mg/kg or 2,3-dimethoxy-1,4-naphthoquinone (DMNQ (25 mg/kg. DMNQ is a more efficient redox cycling agent than DOX but unlike DOX has limited ability to inhibit gene transcription and DNA replication. This allowed specific testing of the redox hypothesis for cardiotoxicity. An acute dose was used to avoid pathophysiological effects in the genomic analysis. However similar data were obtained with a chronic model, but are not specifically presented. All data are deposited in the Gene Expression Omnibus (GEO. Pathway and biochemical analysis of cardiac global gene transcription and mRNA translation data derived at time points from 5 min after an acute exposure in vivo showed a pronounced effect on electron transport chain activity. This led to loss of ATP, increased AMPK expression, mitochondrial genome amplification and activation of caspase 3. No data gathered with either compound indicated general redox damage, though site specific redox damage in mitochondria cannot be entirely discounted. CONCLUSIONS/SIGNIFICANCE: These data indicate the major mechanism of doxorubicin cardiotoxicity is via damage or inhibition of the electron transport chain and not general redox stress. There is a rapid response at transcriptional and translational level of many of the genes coding for proteins of the electron transport chain

  5. Ultra-rapid targeted analysis of 40 drugs of abuse in oral fluid by LC-MS/MS using carbon-13 isotopes of methamphetamine and MDMA to reduce detector saturation.

    Science.gov (United States)

    Di Rago, Matthew; Chu, Mark; Rodda, Luke N; Jenkins, Elizabeth; Kotsos, Alex; Gerostamoulos, Dimitri

    2016-05-01

    The number of oral fluid samples collected by the road policing authority in Victoria, Australia, requiring confirmatory laboratory analysis for drugs proscribed under Victorian legislation (methamphetamine, MDMA and Δ9-tetrahydrocannabinol) has greatly increased in recent years, driving the need for improved analysis techniques to enable expedient results. The aim of this study was to develop an LC-MS/MS-based targeted oral fluid screening technique that covers a broad range of basic and neutral drugs of abuse that can satisfy increased caseload while monitoring other compounds of interest for epidemiological purposes. By combining small sample volume, simple extraction procedure, rapid LC-MS/MS analysis and automated data processing, 40 drugs of abuse including amphetamines, benzodiazepines, cocaine and major metabolites, opioids, cannabinoids and some designer stimulants were separated over 5 min (with an additional 0.5 min re-equilibration time). The analytes were detected using a Sciex® API 4500 Q-Trap LC-MS/MS system with positive ESI in MRM mode monitoring three transitions per analyte. The method was fully validated in accordance with international guidelines and also monitored carbon-13 isotopes of MDMA and MA to reduce detector saturation effects, allowing for confirmation of large concentrations of these compounds without the need for dilution or re-analysis. The described assay has been successfully used for analysis of oral fluid collected as part of law enforcement procedures at the roadside in Victoria, providing forensic results as well as epidemiological prevalence in the population tested. The fast and reliable detection of a broad range of drugs and subsequent automated data processing gives the opportunity for high throughput and fast turnaround times for forensic toxicology.

  6. Isotope-based quantum information

    CERN Document Server

    G Plekhanov, Vladimir

    2012-01-01

    The present book provides to the main ideas and techniques of the rapid progressing field of quantum information and quantum computation using isotope - mixed materials. It starts with an introduction to the isotope physics and then describes of the isotope - based quantum information and quantum computation. The ability to manipulate and control electron and/or nucleus spin in semiconductor devices provides a new route to expand the capabilities of inorganic semiconductor-based electronics and to design innovative devices with potential application in quantum computing. One of the major challenges towards these objectives is to develop semiconductor-based systems and architectures in which the spatial distribution of spins and their properties can be controlled. For instance, to eliminate electron spin decoherence resulting from hyperfine interaction due to nuclear spin background, isotopically controlled devices are needed (i.e., nuclear spin-depleted). In other emerging concepts, the control of the spatial...

  7. A sensitive, selective and rapid determination of lead(II) ions in real-life samples using an electrochemically reduced graphene oxide-graphite reinforced carbon electrode.

    Science.gov (United States)

    Hamsawahini, Kunashegaran; Sathishkumar, Palanivel; Ahamad, Rahmalan; Yusoff, Abdull Rahim Mohd

    2015-11-01

    In this study, a sensitive and cost-effective electrochemically reduced graphene oxide (ErGO) on graphite reinforced carbon (GRC) was developed for the detection of lead (Pb(II)) ions present in the real-life samples. A film of graphene oxide (GO) was drop-casted on GRC and their electrochemical properties were investigated using cyclic voltammetry (CV), amperometry and square wave voltammetry (SWV). Factors influencing the detection of Pb(II) ions, such as grades of GRC, constant applied cathodic potential (CACP), concentration of hydrochloric acid and drop-casting drying time were optimised. GO is irreversibly reduced in the range of -0.7 V to -1.6 V vs Ag/AgCl (3 M) in acidic condition. The results showed that the reduction behaviour of GO contributed to the high sensitivity of Pb(II) ions detection even at nanomolar level. The ErGO-GRC showed the detection limit of 0.5 nM and linear range of 3-15 nM in HCl (1 M). The developed electrode has potential to be a good candidate for the determination of Pb(II) ions in different aqueous system. The proposed method gives a good recovery rate of Pb(II) ions in real-life water samples such as tap water and river water.

  8. Lead discovery for mammalian elongation of long chain fatty acids family 6 using a combination of high-throughput fluorescent-based assay and RapidFire mass spectrometry assay.

    Science.gov (United States)

    Takamiya, Mari; Sakurai, Masaaki; Teranishi, Fumie; Ikeda, Tomoko; Kamiyama, Tsutomu; Asai, Akira

    2016-11-25

    A high-throughput RapidFire mass spectrometry assay is described for elongation of very long-chain fatty acids family 6 (Elovl6). Elovl6 is a microsomal enzyme that regulates the elongation of C12-16 saturated and monounsaturated fatty acids. Elovl6 may be a new therapeutic target for fat metabolism disorders such as obesity, type 2 diabetes, and nonalcoholic steatohepatitis. To identify new Elovl6 inhibitors, we developed a high-throughput fluorescence screening assay in 1536-well format. However, a number of false positives caused by fluorescent interference have been identified. To pick up the real active compounds among the primary hits from the fluorescence assay, we developed a RapidFire mass spectrometry assay and a conventional radioisotope assay. These assays have the advantage of detecting the main products directly without using fluorescent-labeled substrates. As a result, 276 compounds (30%) of the primary hits (921 compounds) in a fluorescence ultra-high-throughput screening method were identified as common active compounds in these two assays. It is concluded that both methods are very effective to eliminate false positives. Compared with the radioisotope method using an expensive (14)C-labeled substrate, the RapidFire mass spectrometry method using unlabeled substrates is a high-accuracy, high-throughput method. In addition, some of the hit compounds selected from the screening inhibited cellular fatty acid elongation in HEK293 cells expressing Elovl6 transiently. This result suggests that these compounds may be promising lead candidates for therapeutic drugs. Ultra-high-throughput fluorescence screening followed by a RapidFire mass spectrometry assay was a suitable strategy for lead discovery against Elovl6.

  9. Effect of silver and indium addition on mechanical properties and indentation creep behavior of rapidly solidified Bi-Sn based lead-free solder alloys

    Energy Technology Data Exchange (ETDEWEB)

    Shalaby, Rizk Mostafa, E-mail: rizk1969@yahoo.co.uk [Mansoura University, Metal Physics Lab., Physics Department, Faculty of Science, Al-Gomhouria Street, Mansoura, P.O.Box 35516 (Egypt)

    2013-01-10

    Mechanical properties and indentation creep of the melt-spun process Bi-42 wt%Sn, Bi-40 wt%Sn-2 wt%In, Bi-40 wt%Sn-2 wt%Ag and Bi-38 wt%Sn-2 wt%In-2 wt%Ag were studied by dynamic resonance technique and Vickers indentation testing at room temperature and compared to that of the traditional Sn-37 wt%Pb eutectic alloy. The results show that the structure of Bi-42 wt%Sn alloy is characterized by the presence of rhombohedral Bi and body centered tetragonal {beta}-Sn. The two ternary alloys exhibit additional constituent phases of intermetallic compounds SnIn{sub 19} for Bi-40 wt%Sn-2 wt%In and {epsilon}-Ag{sub 3}Sn for Bi-40 wt%Sn-2 wt%Ag alloys. Attention has been paid to the role of intermetallic compounds on mechanical and creep behavior. The In and Ag containing solder alloy exhibited a good combination of higher creep resistance, good mechanical properties and lower melting temperature as compared with Pb-Sn eutectic solder alloy. This was attributed to the strengthening effect of Bi as a strong solid solution element in the Sn matrix and formation of intermetallic compounds {beta}-SnBi, {epsilon}-Ag{sub 3}Sn and InSn{sub 19} which act as both strengthening agent and grain refiner in the matrix of the material. Addition of In and Ag decreased the melting temperature of Bi-Sn lead-free solder from 143 Degree-Sign C to 133 Degree-Sign C which was possible mainly due to the existence of InSn{sub 19} and Ag{sub 3}Sn intermetallic compounds. Elastic constants, internal friction and thermal properties of Bi-Sn based alloys have been studied and analyzed.

  10. Characteristics of lead geochemistry and the mobility of Pb isotopes in the system of pedogenic rock-pedosphere-irrigated riverwater-cereal-atmosphere from the Yangtze River delta region, China.

    Science.gov (United States)

    Wang, Cheng; Wang, Jianhua; Yang, Zhongfang; Mao, Changping; Ji, Junfeng

    2013-11-01

    Knowledge of the characteristics of Pb and its isotopic transfer in different compartments is scant, especially for the mobility of Pb isotopes in the geochemical cycle. The present study characterizes differential Pb transport mechanism and the mobility of Pb isotopes in the pedogenic parent rock-pedosphere-irrigated riverwater-cereal-atmosphere system in the Yangtze River delta region, by determining Pb concentration and Pb isotopic ratios of pedogenic parent rocks, fluvial suspended particle matter, tillage soils, soil profiles, irrigated riverwater, fertilizer, Pb ore, cereal roots and grains. The results show that Pb isotopes in the geochemical cycle generally follow the equation of (208)Pb/(206)Pb=-1.157×(206)Pb/(207)Pb+3.46 (r(2)=0.941). However, Pb isotopes have different mobility in different environmental matrixes. Whereas in the pedosphere, the heavier Pb ((208)Pb) usually shows stronger mobility relative to the lighter Pb, and is more likely to transfer into soil exchangeable Pb fraction and carbonates phase. The lighter Pb shows stronger transfer ability from soil to cereal grain via root compared to the heavier Pb. However, the cereal grains have lower (206)Pb/(207)Pb and higher (208)Pb/(206)Pb ratios than root and tillage soil, similar to the airborne Pb and anthropogenic Pb, implying that a considerable amount of Pb in cereal grains comes from the atmosphere. The estimate model shows that 16.7-52.6% (average: 33.5%) of Pb in rice grain is the airborne Pb.

  11. Cryogenic Calcite: A Morphologic and Isotopic Analog to the ALH84001 Carbonates

    Science.gov (United States)

    Niles, P. B.; Leshin, L. A.; Socki, R. A.; Guan, Y.; Ming, D. W.; Gibson, E. K.

    2004-01-01

    Martian meteorite ALH84001 carbonates preserve large and variable microscale isotopic compositions, which in some way reflect their formation environment. These measurements show large variations (>20%) in the carbon and oxygen isotopic compositions of the carbonates on a 10-20 micron scale that are correlated with chemical composition. However, the utilization of these data sets for interpreting the formation conditions of the carbonates is complex due to lack of suitable terrestrial analogs and the difficulty of modeling under non-equilibrium conditions. Thus, the mechanisms and processes are largely unknown that create and preserve large microscale isotopic variations in carbonate minerals. Experimental tests of the possible environments and mechanisms that lead to large microscale isotopic variations can help address these concerns. One possible mechanism for creating large carbon isotopic variations in carbonates involves the freezing of water. Carbonates precipitate during extensive CO2 degassing that occurs during the freezing process as the fluid s decreasing volume drives CO2 out. This rapid CO2 degassing results in a kinetic isotopic fractionation where the CO2 gas has a much lighter isotopic composition causing an enrichment of 13C in the remaining dissolved bicarbonate. This study seeks to determine the suitability of cryogenically formed carbonates as analogs to ALH84001 carbonates. Specifically, our objective is to determine how accurately models using equilibrium fractionation factors approximate the isotopic compositions of cryogenically precipitated carbonates. This includes determining the accuracy of applying equilibrium fractionation factors during a kinetic process, and determining how isotopic variations in the fluid are preserved in microscale variations in the precipitated carbonates.

  12. Researches on the Quantitative Calculation of Uranium Origin and the Lead Isotope Compositions of Precambrian Terrains in the Anshan-Benxi Area%鞍本地区早前寒武纪地质体铅同位素组成及铀源条件定量计算方法研究

    Institute of Scientific and Technical Information of China (English)

    韩军; 李林强; 李月湘; 夏毓亮

    2011-01-01

    This paper studied and compared lead isotope compositions among the different terrains, such as granites,metal deposits, and metamorphic rocks in the Anshan-Benxi area. Figure prospective plumbotectonics model, two stage common lead H-H model, and three stage model were applied to estimate the correspondent isotopic ages.The results indicated that the correspondent isotopic ages are from 2000Ma to 1600Ma. These isotope ages are similar to that of pitchblende. The lead isotope compositions correspond to the different geological settings. The abnormally high compositions of radioactive lead in the Lianshanguan granites implicited that they rich of uranium. The paleoproterozoic granite source and the metal deposit regions, with normal ore lead isotope compositions originated mainly from the metamorphic rocks of the Liaohe group, and both of them underwent the synchronized tectonic and granites remelting events in the early paleoproterozoic. The primitive uranium lost by the granitic rocks results in the uranium metallogenetic zone of the Lianshanguan area.%本文对比了鞍本地区前寒武纪铅一锌一银矿区和铀矿区的硫化物矿石和花岗岩长石Pb同位素组成,分别用矿石铅二阶段普通铅法、铅构造模式图解和全岩铅同位素组成三阶段拟合法计算了年龄和全岩原始铀含量.结果表明,矿石铅和长石铅模式年龄约为2000 Ma,在铅构造模式图上投影于2000~1600 Ma间,花岗岩和辽河群全岩拟合年龄为2000~1800 Ma;铅同位素组成显示铅-锌-银来自早元古代辽河群地层,连山关地区明显为放射性成因Pb同位素组成,源于富铀花岗岩.连山关矿石铅年龄和全岩三阶段年龄与该区铀矿床沥青铀矿的年龄基本一致;花岗岩原始铀的得失计算表明,该地区不同地质体均经历了约2000~1800 Ma花岗岩重熔改造,花岗质岩石发生了铀的丢失,是连山关地区铀矿的主要来源.

  13. Isotopic constraints of mantle derived carbonatitic melts from Calatrava, Spain

    Science.gov (United States)

    Humphreys, E. R.; Bailey, K.; Hawkesworth, C. J.; Wall, F.; Avanzinelli, R.

    2010-12-01

    Carbonatite volcanism is typically associated both spatially and temporally with alkaline, ultramafic volcanism (Woolley & Church, 2005). Recent discoveries in Calatrava, Spain illustrate the activity of carbonatite in the source melts of leucitite volcanism. Melilitite pyroclastic lapilli tuffs also show a clear association with volcanic carbonate. Carbonatitic activity has been shown to initiate at depths greater than 100km (Humphreys et al., 2010) despite a maximum estimate of lithospheric thickness of 80km. The presence of aragonite and abundant mantle xenoliths in many deposits are clear indication of the rapid emplacement rates of such magmas. Carbonatitic activity in the source of the leucitite melts is indicated by carbonate inclusions within olivine xenocrysts and the presence of occasional carbonatite lenses. The composition of lead and strontium isotope ratios in the bulk rock, and spatially resolved analysis of carbonate from the groundmass and from inclusions demonstrates a genetic affinity between the inclusions and the related bulk rock composition. Lead and strontium isotopic analysis suggest that such melts do not represent the composition of convecting asthenospheric mantle. 87Sr/86Sr (0.7055-0.7068) values are higher than those of MORB and most OIB. Lead isotope ratios show a trend displaced to higher 207Pb/204Pb relative to MORB and OIB. Carbonate inclusions have less radiogenic lead values than the more radiogenic bulk rocks. Our data indicate that carbonatitic activity in the mantle is intrinsic in the generation of the leucitite lava. However, petrographic and isotopic evidence suggest a complex melt history. Olivine xenocrysts are not in equilibrium with the host leucitite, despite inclusions within olivine showing an isotopic affinity to the bulk rock. We suggest that in this example, alkaline magmatism was induced by the presence of CO2 in the mantle source. Isotopic evidence shows that the mantle producing such melts was not

  14. Influence of sea ice on ocean water vapor isotopes and Greenland ice core records

    Science.gov (United States)

    Klein, Eric S.; Welker, Jeffrey M.

    2016-12-01

    A warming climate results in sea ice loss and impacts to the Arctic water cycle. The water isotope parameter deuterium excess, a moisture source proxy, can serve as a tracer to help understand hydrological changes due to sea ice loss. However, unlocking the sea ice change signal of isotopes from ice cores requires understanding how sea ice changes impact deuterium excess, which is unknown. Here we present the first isotope data linking a gradient of sea ice extents to oceanic water vapor deuterium excess values. Initial loss of sea ice extent leads to lower deuterium excess moisture sources, and then values progressively increase with further ice loss. Our new process-based interpretation suggests that past rapid (1-3 years) Greenland ice core changes in deuterium excess during warming might not be the result of abrupt atmospheric circulation shifts, but rather gradual loss of sea ice extent at northern latitude moisture sources.

  15. Fluctuations in Precambrian atmospheric oxygenation recorded by chromium isotopes.

    Science.gov (United States)

    Frei, Robert; Gaucher, Claudio; Poulton, Simon W; Canfield, Don E

    2009-09-10

    Geochemical data suggest that oxygenation of the Earth's atmosphere occurred in two broad steps. The first rise in atmospheric oxygen is thought to have occurred between approximately 2.45 and 2.2 Gyr ago, leading to a significant increase in atmospheric oxygen concentrations and concomitant oxygenation of the shallow surface ocean. The second increase in atmospheric oxygen appears to have taken place in distinct stages during the late Neoproterozoic era ( approximately 800-542 Myr ago), ultimately leading to oxygenation of the deep ocean approximately 580 Myr ago, but details of the evolution of atmospheric oxygenation remain uncertain. Here we use chromium (Cr) stable isotopes from banded iron formations (BIFs) to track the presence of Cr(VI) in Precambrian oceans, providing a time-resolved picture of the oxygenation history of the Earth's atmosphere-hydrosphere system. The geochemical behaviour of Cr is highly sensitive to the redox state of the surface environment because oxidative weathering processes produce the oxidized hexavalent [Cr(VI)] form. Oxidation of reduced trivalent [Cr(III)] chromium on land is accompanied by an isotopic fractionation, leading to enrichment of the mobile hexavalent form in the heavier isotope. Our fractionated Cr isotope data indicate the accumulation of Cr(VI) in ocean surface waters approximately 2.8 to 2.6 Gyr ago and a likely transient elevation in atmospheric and surface ocean oxygenation before the first great rise of oxygen 2.45-2.2 Gyr ago (the Great Oxidation Event). In approximately 1.88-Gyr-old BIFs we find that Cr isotopes are not fractionated, indicating a decline in atmospheric oxygen. Our findings suggest that the Great Oxidation Event did not lead to a unidirectional stepwise increase in atmospheric oxygen. In the late Neoproterozoic, we observe strong positive fractionations in Cr isotopes (delta(53)Cr up to +4.9 per thousand), providing independent support for increased surface oxygenation at that time, which may

  16. The isotopic composition of ore lead of the Creede mining district and vicinity, San Juan Mountains, Colorado: Text of a talk presented at the San Juan Mountains symposium to honor Thomas A. Steven; Rocky Mountain Section meeting of the Geological Society of America, May 2, 1987, Boulder, Colorado

    Science.gov (United States)

    Foley, N.K.; Barton, P.B.; Bethke, P.M.; Doe, B.R.

    1988-01-01

    Galenas from the major Creede veins and their northern extensions are remarkably homogeneous in Pb-isotopic composition and are too radiogenic to have been derived from any magma comparable in composition to the principal volcanic rocks. This pattern was identified by Doe et al. in 1979 who proposed that the lead was derived from the Precambrian basement. The homogeneity of the ore leads, however, requires a uniform reservoir; an unlikely prospect for lead from the Precambrian basement. We report on 16 new analyses of geographically and paragenetically dispersed galenas from the Creede district and other areas as far as 11 km to the north. The lead values range from 18.972 to 19.060 for 206Pb/204Pb, from 15.591 to 15.671 for 207Pb/204Pb, and from 37.781 to 37.921 for 208Pb/204Pb. These ranges overlap those previously reported for the main ore zone.

  17. Rapid determination of 226Ra in environmental samples

    Energy Technology Data Exchange (ETDEWEB)

    Maxwell, Sherrod L.; Culligan, Brian K.

    2012-02-04

    A new rapid method for the determination of {sup 228}Ra in natural water samples has been developed at the SRNL/EBL (Savannah River National Lab/ Environmental Bioassay Laboratory) that can be used for emergency response or routine samples. While gamma spectrometry can be employed with sufficient detection limits to determine {sup 228}Ra in solid samples (via {sup 228}Ac) , radiochemical methods that employ gas flow proportional counting techniques typically provide lower MDA (Minimal Detectable Activity) levels for the determination of {sup 228}Ra in water samples. Most radiochemical methods for {sup 228}Ra collect and purify {sup 228}Ra and allow for {sup 228}Ac daughter ingrowth for ~36 hours. In this new SRNL/EBL approach, {sup 228}Ac is collected and purified from the water sample without waiting to eliminate this delay. The sample preparation requires only about 4 hours so that {sup 228}Ra assay results on water samples can be achieved in < 6 hours. The method uses a rapid calcium carbonate precipitation enhanced with a small amount of phosphate added to enhance chemical yields (typically >90%), followed by rapid cation exchange removal of calcium. Lead, bismuth, uranium, thorium and protactinium isotopes are also removed by the cation exchange separation. {sup 228}Ac is eluted from the cation resin directly onto a DGA Resin cartridge attached to the bottom of the cation column to purify {sup 228}Ac. DGA Resin also removes lead and bismuth isotopes, along with Sr isotopes and {sup 90}Y. La is used to determine {sup 228}Ac chemical yield via ICP-MS, but {sup 133}Ba can also be used instead if ICP-MS assay is not available. Unlike some older methods, no lead or strontium holdback carriers or continual readjustment of sample pH is required.

  18. Lead in the western South China Sea: Evidence of atmospheric deposition and upwelling

    Science.gov (United States)

    Chen, Mengli; Goodkin, Nathalie F.; Boyle, Edward A.; Switzer, Adam D.; Bolton, Annette

    2016-05-01

    In recent decades, rapid industrial developments have increased lead (Pb) inputs to the South China Sea. To quantify the increasing variability, we investigated 170 years of skeletal Pb and Pb isotopes from an offshore, central Vietnamese coral. The Pb/Ca in the coral was 10-16 nmol/mol before the mid-1950s and increased to more than 30 nmol/mol by 2000. While the regional phaseout of leaded petrol commenced in 2000, coral Pb/Ca continued increasing until 2004, possibly due to regional upwelling and the transport of previously emitted Pb from tropical Pacific waters. The 206Pb/207Pb ratio in the coral was 1.191-1.195 before mid-1950s, suggesting natural sources. Since then, the ratio decreased, reaching ~1.165 in 2004. Lead isotopes show high linearity between natural and Chinese emitted Pb, with the latter contributing ~40%~60% of the skeletal Pb after 2000.

  19. Geochemistry, geochronology, mineralogy, and geology suggest sources of and controls on mineral systems in the southern Toquima Range, Nye County, Nevada; with geochemistry maps of gold, silver, mercury, arsenic, antimony, zinc, copper, lead, molybdenum, bismuth, iron, titanium, vanadium, cobalt, beryllium, boron, fluorine, and sulfur; and with a section on lead associations, mineralogy and paragenesis, and isotopes

    Science.gov (United States)

    Shawe, Daniel R.; Hoffman, James D.; Doe, Bruce R.; Foord, Eugene E.; Stein, Holly J.; Ayuso, Robert A.

    2003-01-01

    Geochemistry maps showing the distribution and abundance of 18 elements in about 1,400 rock samples, both mineralized and unmineralized, from the southern Toquima Range, Nev., indicate major structural and lithologic controls on mineralization, and suggest sources of the elements. Radiometric age data, lead mineralogy and paragenesis data, and lead-isotope data supplement the geochemical and geologic data, providing further insight into timing, sources, and controls on mineralization. Major zones of mineralization are centered on structural margins of calderas and principal northwest-striking fault zones, as at Round Mountain, Manhattan, and Jefferson mining districts, and on intersections of low-angle and steep structures, as at Belmont mining district. Paleozoic sedimentary rocks, mostly limestones (at Manhattan, Jefferson, and Belmont districts), and porous Oligocene ash-flow tuffs (at Round Mountain district) host the major deposits, although all rock types have been mineralized as evidenced by numerous prospects throughout the area. Principal mineral systems are gold-silver at Round Mountain where about 7 million ounces of gold and more than 4 million ounces of silver has been produced; gold at Gold Hill in the west part of the Manhattan district where about a half million ounces of gold has been produced; gold-mercury-arsenic-antimony in the east (White Caps) part of the Manhattan district where a few hundred thousand ounces of gold has been produced; and silver-lead-antimony at Belmont where more than 150,000 ounces of silver has been produced. Lesser amounts of gold and silver have been produced from the Jefferson district and from scattered mines elsewhere in the southern Toquima Range. A small amount of tungsten was produced from mines in the granite of the Round Mountain pluton exposed east of Round Mountain, and small amounts of arsenic, antimony, and mercury have been produced elsewhere in the southern Toquima Range. All elements show unique

  20. Determination of lead isotopes in a new Greenland deep ice core at the sub-picogram per gram level by thermal ionization mass spectrometry using an improved decontamination method.

    Science.gov (United States)

    Han, Changhee; Burn-Nunes, Laurie J; Lee, Khanghyun; Chang, Chaewon; Kang, Jung-Ho; Han, Yeongcheol; Hur, Soon Do; Hong, Sungmin

    2015-08-01

    An improved decontamination method and ultraclean analytical procedures have been developed to minimize Pb contamination of processed glacial ice cores and to achieve reliable determination of Pb isotopes in North Greenland Eemian Ice Drilling (NEEM) deep ice core sections with concentrations at the sub-picogram per gram level. A PL-7 (Fuso Chemical) silica-gel activator has replaced the previously used colloidal silica activator produced by Merck and has been shown to provide sufficiently enhanced ion beam intensity for Pb isotope analysis for a few tens of picograms of Pb. Considering the quantities of Pb contained in the NEEM Greenland ice core and a sample weight of 10 g used for the analysis, the blank contribution from the sample treatment was observed to be negligible. The decontamination and analysis of the artificial ice cores and selected NEEM Greenland ice core sections confirmed the cleanliness and effectiveness of the overall analytical process.

  1. Rb-Sr whole-rock and mineral ages, K-Ar, 40Ar/39Ar, and U-Pb mineral ages, and strontium, lead, neodymium, and oxygen isotopic compositions for granitic rocks from the Salinian Composite Terrane, California:

    Science.gov (United States)

    Kistler, R.W.; Champion, D.E.

    2001-01-01

    This report summarizes new and published age and isotopic data for whole-rocks and minerals from granitic rocks in the Salinian composite terrane, California. Rubidium-strontium whole-rock ages of plutons are in two groups, Early Cretaceous (122 to 100 Ma) and Late Cretaceous (95 to 82 Ma). Early Cretaceous plutons occur in all granitic rock exposures from Bodega Head in the north to those from the Santa Lucia and Gabilan Ranges in the central part of the terrane. Late Cretaceous plutons have been identified in the Point Reyes Peninsula, the Santa Lucia and the Gabilan Ranges, and in the La Panza Range in the southern part of the terrane. Ranges of initial values of isotopic compositions are 87Sr/86Sr, 0.7046-0.7147, δ18O, +8.5 to +12.5 per mil, 206Pb/204Pb, 18.901-19.860, 207Pb/204Pb, 15.618-15.814, 208Pb/204Pb, 38.569- 39.493, and εNd, +0.9 to -8.6. The initial 87Sr/86Sr=0.706 isopleth is identified in the northern Gabilan Range and in the Ben Lomond area of the Santa Cruz Mountains, in Montara Mountain, in Bodega Head, and to the west of the Farallon Islands on the Cordell Bank. This isotopic boundary is offset about 95 miles (160km) by right-lateral displacements along the San Gregorio-Hosgri and San Andreas fault systems.

  2. 云南兰坪盆地西缘脉状铜多金属矿床硫、铅同位素组成及成矿示踪%Sulfur and lead isotope compositions and tracing of copper deposits on the western border of the Lanping Basin, Yunnan Province

    Institute of Scientific and Technical Information of China (English)

    张锦让; 温汉捷

    2012-01-01

    云南兰坪盆地西缘脉状铜多金属矿床主要赋存于由砂岩、粉砂岩和页岩组成的碎屑岩建造中.为了查明兰坪盆地西缘脉状铜多金属矿床成矿物质来源,对盆地西缘四个典型脉状铜多金属矿床(科登涧、连城、金满和水泄)的硫、铅同位素的组成进行了分析和对比研究.结果表明,这些矿床的铅同位素组成总体变化较小,且大部分落在盆地沉积地层铅范围内,金满、连城铜矿床可能有部分深源铅的加入.硫同位素特征表明,兰坪盆地西缘脉状铜多金属矿床的硫主要来源于地层硫酸盐的还原作用,其中金满铜矿床和连城铜钼多金属矿床可能有深源硫的混入.各矿床硫同位素不同的特点,除反映各矿床源区硫同位素组成的差异外,可能还与各矿床成矿时不同的物理化学条件(温度、氧逸度、pH值和离子强度等)差异有关.%A large number of vein-type Cu-polymetallic deposits were developed on the western border of the Lanping Basin in western Yunnan Province, which constituted an important Cu-polymetallic mineralization belt. These deposits are hosted in clastic rocks (sandstone, siltite and argillite) of Mesozoic and Cenozoic formation. In order to trace source of ore-forming materials of these deposits, four representative deposits (Jinman, Shuixie, Kedengjian and Liancheng) were selected to analyze sulfur and lead isotopic compositions. Pb isotopic compositions show very narrow variations and mostly fall within the range of the sedimentary rock lead, suggesting that lead in these vein-type Cu-polymetallic deposits is mostly derived from the basement of the basin. However, the Jinman and Liancheng deposits may have deep sources of lead with different Pb isotopic composition. Sulfur isotope analysis show that the reduced sulfur of these vein-type Cu-polymetallic deposits mainly come from the strata sulfate. However, like Pb isotopes, the Jinman and Liancheng deposits have more

  3. Deciphering petrogenic processes using Pb isotope ratios from time-series samples at Bezymianny and Klyuchevskoy volcanoes, Central Kamchatka Depression

    Science.gov (United States)

    Kayzar, Theresa M.; Nelson, Bruce K.; Bachmann, Olivier; Bauer, Ann M.; Izbekov, Pavel E.

    2014-10-01

    The Klyuchevskoy group of volcanoes in the Kamchatka arc erupts compositionally diverse magmas (high-Mg basalts to dacites) over small spatial scales. New high-precision Pb isotope data from modern juvenile (1956-present) erupted products and hosted enclaves and xenoliths from Bezymianny volcano reveal that Bezymianny and Klyuchevskoy volcanoes, separated by only 9 km, undergo varying degrees of crustal processing through independent crustal columns. Lead isotope compositions of Klyuchevskoy basalts-basaltic andesites are more radiogenic than Bezymianny andesites (208Pb/204Pb = 37.850-37.903, 207Pb/204Pb = 15.468-15.480, and 206Pb/204Pb = 18.249-18.278 at Bezymianny; 208Pb/204Pb = 37.907-37.949, 207Pb/204Pb = 15.478-15.487, and 206Pb/204Pb = 18.289-18.305 at Klyuchevskoy). A mid-crustal xenolith with a crystallization pressure of 5.2 ± 0.6 kbars inferred from two-pyroxene geobarometry and basaltic andesite enclaves from Bezymianny record less radiogenic Pb isotope compositions than their host magmas. Hence, assimilation of such lithologies in the middle or lower crust can explain the Pb isotope data in Bezymianny andesites, although a component of magma mixing with less radiogenic mafic recharge magmas and possible mantle heterogeneity cannot be excluded. Lead isotope compositions for the Klyuchevskoy Group are less radiogenic than other arc segments (Karymsky—Eastern Volcanic Zone; Shiveluch—Northern Central Kamchatka Depression), which indicate increased lower-crustal assimilation beneath the Klyuchevskoy Group. Decadal timescale Pb isotope variations at Klyuchevskoy demonstrate rapid changes in the magnitude of assimilation at a volcanic center. Lead isotope data coupled with trace element data reflect the influence of crustal processes on magma compositions even in thin mafic volcanic arcs.

  4. Chemical Pre-treatment Methods for Measurement of Ge Isotopic Ratio on Sphalerite in Lead-Zinc Deposits%铅锌矿床地质样品的Ge同位素预处理方法研究

    Institute of Scientific and Technical Information of China (English)

    朱传威; 温汉捷; 樊海峰; 张羽旭; 刘洁; 杨涛; 王光辉

    2014-01-01

    Up to the present,main research of Ge isotopes has been carried out on organic,magmatic and meteoritic samples. Pb-Zn deposits are one of the most important reservoirs of Ge;however,there are few studies on Ge isotopes for these samples. Ge separation and purification for samples collected from Pb-Zn deposits are the basis of Ge isotope research. Therefore,the suitability for Pb-Zn ores of the Ge isotopic purification method established for meteoritic samples in details has been investigated. The results demonstrate that anion exchange resins single-column method for Pb-Zn ores can eliminate the potential interferences efficiently( including Fe,Se and other interfering matrix elements),but does not work for Zn as Zn/Ge﹥3,indicating that further separation and purification by ion-exchange column are needed to eliminate Zn. Conditional experiments of standard samples ( ores and sphalerite)and three sphalerite samples from the Fule deposits showed that adjusting the volume of anion exchange resin elution acid(1. 4 mol/L,HNO3 )from 6 mL to 10 mL and maintaining the method of cation exchange resin is suitable for Ge isotope purification. The results of anion/cation exchange resin two-column procedure indicate that the recovery of Ge was better than 99%,and the potential interferences on Ge isotopes ( including Fe,Se,Zn and other interfering matrix elements)were almost 100% eliminated. Although the previous method has a good recovery of Ge(97. 3%)and the potential interferences on Ge isotopes(including Fe,Se,Zn and other interfering matrix elements ) were reduced to the negligible levels,the recovery is lower than the recommended method in this paper. Furthermore,the Ge isotopic composition of three sphalerite samples from the Fule deposit show that there are no signals coming from interfering elements and matrix elements,and the mass fractionation of Ge isotope followed the rule of mass-dependent fractionation. Overall,this modified method for Ge isotope measurement

  5. Stable isotope studies

    Energy Technology Data Exchange (ETDEWEB)

    Ishida, T.

    1992-01-01

    The research has been in four general areas: (1) correlation of isotope effects with molecular forces and molecular structures, (2) correlation of zero-point energy and its isotope effects with molecular structure and molecular forces, (3) vapor pressure isotope effects, and (4) fractionation of stable isotopes. 73 refs, 38 figs, 29 tabs.

  6. Paleoproxies: Heavy Stable Isotope Perspectives

    Science.gov (United States)

    Nagler, T. F.; Hippler, D.; Siebert, C.; Kramers, J. D.

    2002-12-01

    Recent advances in isotope ratio mass spectrometry, namely multiple collector ICP-MS and refined TIMS techniques, will significantly enhance the ability to measure heavy stable isotope fractionation, which will lead to the development of a wide array of process-identifying (bio)-geochemical tools. Thus far research in this area is not easily assessable to scientists outside the isotope field. This is due to the fact that analyzing heavy stable isotopes does not provide routine numbers which are per se true (the preciser the truer) but is still a highly experimental field. On the other hand resolving earth science problems requires specialists familiar with the environment being studied. So what is in there for paleoceanographers? In a first order approach, relating isotope variations to physical processes is straightforward. A prominent example are oxygen isotope variations with temperature. The total geological signal is of course far more complicated. At low temperatures, heavy stable isotopes variations have been reported for e.g. Ca, Cr, Fe, Cu, Zn, Mo and Tl. Fractionation mechanisms and physical parameters responsible for the observed variations are not yet resolved for most elements. Significant equilibrium isotope fractionation is expected from redox reactions of transition metals. However a difference in coordination number between two coexisting speciations of an element in the same oxidation state can also cause fractionation. Protonation of dissolved Mo is one case currently discussed. For paleoceanography studies, a principal distinction between transition metals essential for life (V to Zn plus Mo) or not will be helpful. In case of the former group, distinction between biogenic and abiogenic isotope fractionation will remain an important issue. For example, abiotic Fe redox reactions result in isotope fractionations indistinguishable in direction and magnitude from microbial effects. Only a combination of different stable isotope systems bears the

  7. Sources and characteristics of lead pollution in the urban environment of Guangzhou.

    Science.gov (United States)

    Duzgoren-Aydin, Nurdan S

    2007-10-15

    Guangzhou, the capital of the southeastern province of Guangdong, is one of the largest and most rapidly developing industrial cities in China. In recent years its rapid economic development has brought great prosperity to the Pearl River Delta (PRD) region, but has also given rise to a wide variety of environmental problems. The current level of lead (Pb) contamination (75-926 mg/kg) in the surface environment of Guangzhou remains a major concern, even though the use of leaded petrol in the city was banned in 1997. The Pb isotope ratios (206Pb/207Pb(min-max) : 1.1612-1.1961 and 208Pb/207Pb(min-max) : 2.4495-2.4838) of the urban dusts from unconfined (road dusts and gully sediments) and relatively confined (vehicular tunnel) settings in Guangzhou remains in a relatively narrow range, comparable with those of the regional natural and anthropogenic sources. This study highlights the inherent shortcomings of the Pb isotope fingerprinting technique for provenancing Pb sources, as both the target media (urban dusts) and potential sources have similar and highly radiogenic Pb isotope values. This could not only lead to an overestimation of the effectiveness of phasing-out of leaded petrol, but also an underestimation of the ever-increasing relative contributions from other potential sources of pollution, including coal combustion, industrial emissions of local Pb-ores and non-additive Pb contents of crude oils. Re-suspended Pb-bearing particulates deposited from early vehicular exhaust emission of leaded petrol with distinctly low Pb isotope compositions are still an important source of Pb pollution in the region.

  8. Lead Poisoning

    Science.gov (United States)

    Lead is a metal that occurs naturally in the earth's crust. Lead can be found in all parts of our ... from human activities such as mining and manufacturing. Lead used to be in paint; older houses may ...

  9. Second international conference on isotopes. Conference proceedings

    Energy Technology Data Exchange (ETDEWEB)

    Hardy, C.J. [ed.

    1997-10-01

    The Second International Conference on Isotopes (2ICI) was hosted by the Australian Nuclear Association in Sydney, NSW, Australia. The Theme of the Second Conference: Isotopes for Industry, Health and a Better Environment recognizes that isotopes have been used in these fields successfully for many years and offer prospects for increasing use in the future. The worldwide interest in the use of research reactors and accelerators and in applications of stable and radioactive isotopes, isotopic techniques and radiation in industry, agriculture, medicine, environmental studies and research in general, was considered. Other radiation issues including radiation protection and safety were also addressed. International and national overviews and subject reviews invited from leading experts were included to introduce the program of technical sessions. The invited papers were supported by contributions accepted from participants for oral and poster presentation. A Technical Exhibition was held in association with the Conference. This volume contains the full text or extended abstracts of papers number 61- to number 114

  10. Lead Toxicity

    Science.gov (United States)

    ... including some imported jewelry. What are the health effects of lead? • More commonly, lower levels of lead in children over time may lead to reduced IQ, slow learning, Attention Deficit Hyperactivity Disorder (ADHD), or behavioral issues. • Lead also affects other ...

  11. Production Situation and Technology Prospect of Medical Isotopes

    Directory of Open Access Journals (Sweden)

    GAO Feng;LIN Li;LIU Yu-hao;MA Xing-jun

    2016-10-01

    Full Text Available The isotope production technology was overviewed, including traditional and newest technology. The current situation of medical isotope production was introduced. The problems faced by isotope supply and demand were analyzed. The future development trend of medical isotopes and technology prospect were put forward. As the most populous country, nuclear medicine develops rapidly, however, domestic isotope mainly relies on imports. The highly productive and relatively safe MIPR is expected to be an effective way to breakthrough the bottleneck of the development of nuclear medicine. Traditional isotope production technologies with reactor can be improved. It's urgent to research and promote new isotope production technologies with reactor. Those technologies which do not depend on reactor will have a bright market prospects.

  12. Lead Aprons Are a Lead Exposure Hazard.

    Science.gov (United States)

    Burns, Kevin M; Shoag, Jamie M; Kahlon, Sukhraj S; Parsons, Patrick J; Bijur, Polly E; Taragin, Benjamin H; Markowitz, Morri

    2017-05-01

    To determine whether lead-containing shields have lead dust on the external surface. Institutional review board approval was obtained for this descriptive study of a convenience sample of 172 shields. Each shield was tested for external lead dust via a qualitative rapid on-site test and a laboratory-based quantitative dust wipe analysis, flame atomic absorption spectrometry (FAAS). The χ(2) test was used to test the association with age, type of shield, lead sheet thickness, storage method, and visual and radiographic appearance. Sixty-three percent (95% confidence interval [CI]: 56%-70%) of the shields had detectable surface lead by FAAS and 50% (95% CI: 43%-57%) by the qualitative method. Lead dust by FAAS ranged from undetectable to 998 μg/ft(2). The quantitative detection of lead was significantly associated with the following: (1) visual appearance of the shield (1 = best, 3 = worst): 88% of shields that scored 3 had detectable dust lead; (2) type of shield: a greater proportion of the pediatric patient, full-body, and thyroid shields were positive than vests and skirts; (3) use of a hanger for storage: 27% of shields on a hanger were positive versus 67% not on hangers. Radiographic determination of shield intactness, thickness of interior lead sheets, and age of shield were unrelated to presence of surface dust lead. Sixty-three percent of shields had detectable surface lead that was associated with visual appearance, type of shield, and storage method. Lead-containing shields are a newly identified, potentially widespread source of lead exposure in the health industry. Copyright © 2016 American College of Radiology. Published by Elsevier Inc. All rights reserved.

  13. ESTIMATING THE TIMING OF DIET SHIFTS USING STABLE ISOTOPES

    Science.gov (United States)

    Stable isotope analysis has become an important tool in studies of trophic food webs and animal feeding patterns. When animals undergo rapid dietary shifts due to migration, metamorphosis, or other reasons, the isotopic composition of their tissues begins changing to reflect tha...

  14. Study of the production of neutron-rich isotope beams issuing from fissions induced by fast neutrons; Etude de la production de faisceaux riches en neutrons par fission induite par neutrons rapides

    Energy Technology Data Exchange (ETDEWEB)

    Lau, Ch

    2000-09-15

    This work is a contribution to the PARRNe project (production of radioactive neutron-rich isotopes). This project is based on the fission fragments coming from the fission of 238-uranium induced by fast neutrons. The fast neutron flux is produced by the collisions of deutons in a converter. Thick targets of uranium carbide and liquid uranium targets have been designed in order to allow a quick release of fission fragments. A device, able to trap on a cryogenic thimble rare gas released by the target, has allowed the production of radioactive nuclei whose half-life is about 1 second. This installation has been settled to different deuton accelerators in the framework of the European collaboration SPIRAL-2. A calibration experiment has proved the feasibility of fixing an ISOL-type isotope separator to a 15 MV tandem accelerator, this installation can provide 500 nA deutons beams whose energy is 26 MeV and be a valuable tool for studying fast-neutron induced fission. Zinc, krypton, rubidium, cadmium, iodine, xenon and cesium beams have been produced in this installation. The most intense beams reach 10000 nuclei by micro-coulomb for 26 MeV deutons. An extra gain of 2 magnitude orders can be obtained by using a more specific ion source and by increasing the thickness of the target. Another extra gain of 2 magnitude orders involves 100 MeV deutons.

  15. The Facility for Rare Isotope Beams

    Directory of Open Access Journals (Sweden)

    Wrede C.

    2015-01-01

    Full Text Available The Facility for Rare Isotope Beams (FRIB is a United States Department of Energy user facility currently under construction on the campus of Michigan State University. Based on a 400 kW, 200 MeV/u heavy-ion driver linac, FRIB will deliver high-quality fast, thermalized, and re-accelerated beams of rare isotopes with unprecedented intensities to a variety of experimental areas and equipment. New science opportunities at the frontiers of nuclear structure, nuclear astrophysics, fundamental symmetries, and societal applications will be enabled by this future world-leading rare-isotope beam facility.

  16. The Facility for Rare Isotope Beams

    Science.gov (United States)

    Wrede, C.

    2015-05-01

    The Facility for Rare Isotope Beams (FRIB) is a United States Department of Energy user facility currently under construction on the campus of Michigan State University. Based on a 400 kW, 200 MeV/u heavy-ion driver linac, FRIB will deliver high-quality fast, thermalized, and re-accelerated beams of rare isotopes with unprecedented intensities to a variety of experimental areas and equipment. New science opportunities at the frontiers of nuclear structure, nuclear astrophysics, fundamental symmetries, and societal applications will be enabled by this future world-leading rare-isotope beam facility.

  17. The terrestrial uranium isotope cycle.

    Science.gov (United States)

    Andersen, Morten B; Elliott, Tim; Freymuth, Heye; Sims, Kenneth W W; Niu, Yaoling; Kelley, Katherine A

    2015-01-15

    Changing conditions on the Earth's surface can have a remarkable influence on the composition of its overwhelmingly more massive interior. The global distribution of uranium is a notable example. In early Earth history, the continental crust was enriched in uranium. Yet after the initial rise in atmospheric oxygen, about 2.4 billion years ago, the aqueous mobility of oxidized uranium resulted in its significant transport to the oceans and, ultimately, by means of subduction, back to the mantle. Here we explore the isotopic characteristics of this global uranium cycle. We show that the subducted flux of uranium is isotopically distinct, with high (238)U/(235)U ratios, as a result of alteration processes at the bottom of an oxic ocean. We also find that mid-ocean-ridge basalts (MORBs) have (238)U/(235)U ratios higher than does the bulk Earth, confirming the widespread pollution of the upper mantle with this recycled uranium. Although many ocean island basalts (OIBs) are argued to contain a recycled component, their uranium isotopic compositions do not differ from those of the bulk Earth. Because subducted uranium was probably isotopically unfractionated before full oceanic oxidation, about 600 million years ago, this observation reflects the greater antiquity of OIB sources. Elemental and isotope systematics of uranium in OIBs are strikingly consistent with previous OIB lead model ages, indicating that these mantle reservoirs formed between 2.4 and 1.8 billion years ago. In contrast, the uranium isotopic composition of MORB requires the convective stirring of recycled uranium throughout the upper mantle within the past 600 million years.

  18. Lead exposure in Nunavik: from research to action

    Directory of Open Access Journals (Sweden)

    Ariane Couture

    2012-07-01

    Full Text Available Background. In 1999, the Government of Canada regulated the use of lead shot for hunting. Concurrently, the Nunavik Regional Board of Health and Social Services (NRBHSS was informed of the results of an isotope study that pointed to lead ammunition as a likely source of lead exposure in Nunavik. Rapidly thereafter, a coalition for the banning of lead shot was implemented by the NRBHSS as well as by regional/local partners and by Inuit hunters in order to disseminate this information to the public. Objectives. The purpose of this article is to describe the intervention conducted in the winter of 1999 by the NRBHSS and to assess the combined impact of national legislation and an awareness campaign on blood lead levels in Nunavik. Study design. Impact assessment of the intervention for the banning of lead shot conducted in 1999 in Nunavik using blood lead levels data before and after the intervention. Methods. Data on blood lead levels in Nunavik describing foetal exposure as well as during childhood and in adults published between 1992 and 2009 were compiled. Blood lead levels in Nunavik prior to and after the interventions were compared. To assess the current situation, the most recent blood lead levels were compared with those from surveys conducted during the same period in North America. Results. Analysis of blood samples collected from umbilical cord and from adults show that blood lead levels in Nunavik significantly declined between 1992 and 2004. Nevertheless, lead exposure in Nunavik still remains higher in comparison to that observed in other North American surveys. Conclusions. The current situation regarding lead exposure in Nunavik has significantly improved as a result of the implemented intervention. However, according to recent data, a gap still subsists relative to other North American populations.

  19. Lead Poisoning

    Science.gov (United States)

    ... lead is of microscopic size, invisible to the naked eye. More often than not, children with elevated ... majority of the childhood lead poisoning cases we see today. Children and adults too can get seriously ...

  20. Nuclear Astrophysics with rare isotopes at FRIB

    Science.gov (United States)

    Schatz, Hendrik

    2011-05-01

    The Facility for Rare Isotope Beams (FRIB) currently under construction at Michigan State University will be one of the worlds’ most powerful accelerators to produce rare isotopes. These isotopes live only fractions of seconds, but their properties are imprinted onto the composition of the visible universe and the nature of stellar explosions. FRIB will produce for the first time many of the rare isotopes that are part of the rapid neutron capture process, responsible for the origin of heavy elements; it will measure reaction rates that govern stellar explosions such as supernovae, novae, and X-ray bursts; and it will produce the same exotic nuclei that form the crust of neutron stars. I will discuss how data from FRIB, together with new observational data, promise to address many open questions at the intersection of nuclear physics and astronomy, including the chemical evolution of our Galaxy, the nuclear energy sources of stellar explosions, and the nature of neutron stars.

  1. 电感耦合等离子体质谱法分析大鼠血、毛发及脏器中铅浓度及同位素比值%Determination of Lead Concentration and Isotopic Ratios of Blood, Hair and Tissues in Rats by Inductively Coupled Plasma Mass Spectrometry

    Institute of Scientific and Technical Information of China (English)

    曾静; 闫赖赖; 欧阳荔; 王京宇

    2011-01-01

    建立了电感耦合等离子体质谱(ICP-MS)同时测定铅浓度及同位素比值的方法,并应用于染毒大鼠血、毛发及组织脏器测定,以考察大鼠体内铅浓度及同位素比值分布情况及染毒剂量对其的影响.标准物质牛全血铅浓度测定结果为(278±4) μg/L,在证书标准值(283±18)μg/L范围内;测定10 μg/L Pb标准溶液的RSD肾>毛>肝>全血,各组织脏器中铅同位素指纹亦有不同.血铅相对于毛发铅更适于作为反映体内铅蓄积程度的生物标志物.%A method was developed to simultaneously determine lead concentration and lead isotopic ratios in blood, hair, and other organs of lead exposed rats by inductively coupled plasma mass spec-trometry(ICP-MS). The measurement value of lead concentration in standard material is (278±4) μg/L that is in the range of certified value (283±18) μg/L, and the RSDs of Pb concentration, ratio 204Pb/206Pb, 207Pb/206Pb and 208Pb/206Pb of in the determination of 10 μg/L Pb standard solution were less than 0. 7%, 0. 3%, 0. 15% and 0. 15%, respectively. It was found that RSD of isotopic ratios is stable when Pb concentration is more than 8 μg/L; The concentration calculated by sum of of all Pb isotopes is more accurate and reasonable than that only by 208Pb. The measured results of samples from rats tissues show that there is a selective accumulation of Pb in different tissues and organs, Pb concentration from high to low is in femur, kidney, hair, liver and blood. Blood is more suitable than hair for biomarker to reflect inner Pb accumulation.

  2. Relational Leading

    DEFF Research Database (Denmark)

    2015-01-01

    This first chapter presents the exploratory and curious approach to leading as relational processes – an approach that pervades the entire book. We explore leading from a perspective that emphasises the unpredictable challenges and triviality of everyday life, which we consider an interesting......, relevant and realistic way to examine leading. The chapter brings up a number of concepts and contexts as formulated by researchers within the field, and in this way seeks to construct a first understanding of relational leading....

  3. METHOD OF ISOTOPE CONCENTRATION

    Science.gov (United States)

    Spevack, J.S.

    1957-04-01

    An isotope concentration process is described which consists of exchanging, at two or more different temperature stages, two isotopes of an element between substances that are physically separate from each other and each of which is capable of containing either of the isotopes, and withdrawing from a point between at least two of the temperatare stages one of the substances containing an increased concentration of the desired isotope.

  4. Statistical clumped isotope signatures

    NARCIS (Netherlands)

    Röckmann, T.; Popa, M. E.; Krol, M. C.; Hofmann, M. E. G.

    2016-01-01

    High precision measurements of molecules containing more than one heavy isotope may provide novel constraints on element cycles in nature. These so-called clumped isotope signatures are reported relative to the random (stochastic) distribution of heavy isotopes over all available isotopocules of a m

  5. Application of a stable isotope technique to determine the simultaneous uptake of cadmium, copper, nickel, lead, and zinc by the water flea Daphnia magna from water and the green algae Pseudokirchneriella subcapitata.

    Science.gov (United States)

    Komjarova, Irina; Blust, Ronny

    2009-08-01

    Accumulation and toxicological effects of water and dietary metals in aquatic organisms can potentially be very different. Therefore, it is important to know the relative contribution of these different sources to metal exposure, availability, and accumulation. In the present study, a stable isotope technique was applied to investigate the uptake of Cd, Cu, Ni, Pb, and Zn by the green alga Pseudokirchneriella subcapitata and the water flea Daphnia magna during simultaneous exposure to the five metals at environmentally realistic concentrations from separate water and dietary routes. Green algae take up Cu faster compared to Cd, Ni, Pb, and Zn, and the distribution of metals between the external and internal compartments is dependent on metal and population growth stage. The metal accumulation reached a steady state within 24 to 48 h for all metals. Metal uptake rate constants from water were highest for Cu and lowest for Ni. Metal assimilation efficiencies from the food source varied with metal, ranging from approximately 80% in the case of Cd to near 0% in the case of Ni. Because the data for the different metals were obtained on the same multimetal-exposed organisms, the results are directly comparable among the metals. For all five metals studied, water appeared to be the most important route of uptake by D. magna.

  6. Generation of Radixenon Isotopes

    Energy Technology Data Exchange (ETDEWEB)

    McIntyre, Justin I.; Bowyer, Ted W.; Hayes, James C.; Heimbigner, Tom R.; Morris, Scott J.; Panisko, Mark E.; Pitts, W. K.; Pratt, Sharon L.; Reeder, Paul L.; Thomas, Charles W.

    2003-06-30

    Pacific Northwest National Laboratory has developed an automated system for separating Xe from air and can detect the following radioxenon isotopes, 131mXe, 133mXe, 133Xe, and 135Xe. This report details the techniques used to generate the various radioxenon isotopes that are used for the calibration of the detector as well as other isotopes that have the potential to interfere with the fission produced radioxenon isotopes. Fission production is covered first using highly enriched uranium followed by a description and results from an experiment to produce radioxenon isotopes from neutron activation of ambient xenon.

  7. Isotopes in heterogeneous catalysis

    CERN Document Server

    Hargreaves, Justin SJ

    2006-01-01

    The purpose of this book is to review the current, state-of-the-art application of isotopic methods to the field of heterogeneous catalysis. Isotopic studies are arguably the ultimate technique in in situ methods for heterogeneous catalysis. In this review volume, chapters have been contributed by experts in the field and the coverage includes both the application of specific isotopes - Deuterium, Tritium, Carbon-14, Sulfur-35 and Oxygen-18 - as well as isotopic techniques - determination of surface mobility, steady state transient isotope kinetic analysis, and positron emission profiling.

  8. Isotope Effects of Solid Hydrogenic Pellet Ablation in Fusion Plasma

    Institute of Scientific and Technical Information of China (English)

    PENGLilin; DENGBaiquan; YANJiancheng; WANGXiaoyu

    2003-01-01

    The isotope effects of ablation processes in fusion plasma for five combinations of solid isotopic hydrogenic pellets H2, HD, D2,DT, T2 have been first time studied. The resuits show that the modifications caused by isotope effects for pellet erosion speeds range from 1 for hydrogen pellet down to 0. 487 for tritium pellet and are not negligible in ablation rate calculations. These effects lead to deeper mass deposition and improved core fueling efficiency.

  9. Lead Test

    Science.gov (United States)

    ... months, and at 3, 4, 5, and 6 years of age. A blood lead level test should be done only if the risk ... recommended if the person is symptomatic at any level below 70 mcg/dL. Because lead will pass through the blood to an unborn child, pregnant ...

  10. Laser Spectroscopy of Neutron Rich Bismuth Isotopes

    CERN Multimedia

    2002-01-01

    %IS344 :\\\\ \\\\ The aim of the experiment is to measure the optical isotope shifts and hyperfine structures of bismuth isotopes across the N=126 shell closure in order to extract the change in mean square charge radii ($\\delta\\langle r^{2}\\rangle$) and static moments. These include the first isotones of lead to be measured directly above the shell closure and will provide new information on the systematics of the kink ($\\delta\\langle r^{2}\\rangle)$ seen in the lead isotopic chain. After two very successful runs the programme has been extended to include the neutron deficient isotopes below $^{201}$Bi to study the systematics across the $i_{13/2}$ neutron sub-shell closure at N=118.\\\\ \\\\ During the initial 2 runs (9 shifts) the isotope shifts and hyperfine structures of three new isotopes, $ ^{210,212,213}$Bi and the 9$^{-}$ isomer of $^{210}$Bi have been measured. The accuracy of the previous measurements of $^{205,206,208}$Bi have been greatly improved. The samples of $ ^{208,210,210^{m}}$Bi were prepared by c...

  11. Beam delivery for stable isotope separation

    Science.gov (United States)

    Forbes, Andrew; Strydom, Hendrick J.; Botha, Lourens R.; Ronander, Einar

    2002-10-01

    In the multi-photon dissociation process of Carbon isotope enrichment, IR photons are used to selectively excite a molecule with the given isotopic base element. This enrichment process is very sensitive to the beam's intensity and wavelength. Because the intensity is determined by the propagation of the field, the enrichment factors are also very dependent on the field propagation. In this paper, the influence of the wavelength and intensity of the beam, on the isotope selective dissociation of a CFC compound is investigated both experimentally and theoretically. Consideration is also given to some of the factors that influence the delivery of various beams to the reactor chamber, and their subsequent propagation through the reactor. The results show that suitable beam forming can lead to an improved isotope separation process.

  12. Nitrogen cycling in shallow low-oxygen coastal waters off Peru from nitrite and nitrate nitrogen and oxygen isotopes

    Science.gov (United States)

    Hu, Happy; Bourbonnais, Annie; Larkum, Jennifer; Bange, Hermann W.; Altabet, Mark A.

    2016-03-01

    O2 deficient zones (ODZs) of the world's oceans are important locations for microbial dissimilatory nitrate (NO3-) reduction and subsequent loss of combined nitrogen (N) to biogenic N2 gas. ODZs are generally coupled to regions of high productivity leading to high rates of N-loss as found in the coastal upwelling region off Peru. Stable N and O isotope ratios can be used as natural tracers of ODZ N-cycling because of distinct kinetic isotope effects associated with microbially mediated N-cycle transformations. Here we present NO3- and nitrite (NO2-) stable isotope data from the nearshore upwelling region off Callao, Peru. Subsurface oxygen was generally depleted below about 30 m depth with concentrations less than 10 µM, while NO2- concentrations were high, ranging from 6 to 10 µM, and NO3- was in places strongly depleted to near 0 µM. We observed for the first time a positive linear relationship between NO2-δ15N and δ18O at our coastal stations, analogous to that of NO3- N and O isotopes during NO3- uptake and dissimilatory reduction. This relationship is likely the result of rapid NO2- turnover due to higher organic matter flux in these coastal upwelling waters. No such relationship was observed at offshore stations where slower turnover of NO2- facilitates dominance of isotope exchange with water. We also evaluate the overall isotope fractionation effect for N-loss in this system using several approaches that vary in their underlying assumptions. While there are differences in apparent fractionation factor (ɛ) for N-loss as calculated from the δ15N of NO3-, dissolved inorganic N, or biogenic N2, values for ɛ are generally much lower than previously reported, reaching as low as 6.5 ‰. A possible explanation is the influence of sedimentary N-loss at our inshore stations which incurs highly suppressed isotope fractionation.

  13. Rapid detection and characterization of reactive drug metabolites in vitro using several isotope-labeled trapping agents and ultra-performance liquid chromatography/time-of-flight mass spectrometry.

    Science.gov (United States)

    Rousu, Timo; Pelkonen, Olavi; Tolonen, Ari

    2009-03-01

    Reactive metabolites are believed to be one of the main reasons for unexpected drug-induced toxicity issues, by forming covalent adducts with cell proteins or DNA. Due to their high reactivity and short lifespan they are not directly detected by traditional analytical methods, but are most traditionally analyzed by liquid chromatography/tandem mass spectrometry (LC/MS/MS) after chemical trapping with nucleophilic agents such as glutathione. Here, a simple but very efficient assay was built up for screening reactive drug metabolites, utilizing stable isotope labeled glutathione, potassium cyanide and semicarbazide as trapping agents and highly sensitive ultra-performance liquid chromatography/time-of-flight mass spectrometry (UPLC/TOFMS) as an analytical tool. A group of twelve structurally different compounds was used as a test set, and a large number of trapped metabolites were detected for most of them, including many conjugates not reported previously. Glutathione-trapped metabolites were detected for nine of the twelve test compounds, whereas cyanide-trapped metabolites were found for eight and semicarbazide-trapped for three test compounds. The high mass accuracy of TOFMS provided unambiguous identification of change in molecular formula by formation of a reactive metabolite. In addition, use of a mass defect filter was found to be a usable tool when mining the trapped conjugates from the acquired data. The approach was shown to provide superior detection sensitivity in comparison to traditional methods based on neutral loss or precursor ion scanning with a triple quadrupole mass spectrometer, and clearly more efficient detection and characterization of reactive drug metabolites with a simpler test setup. Copyright (c) 2009 John Wiley & Sons, Ltd.

  14. Archives of Atmospheric Lead Pollution

    Science.gov (United States)

    Weiss, Dominik; Shotyk, William; Kempf, Oliver

    Environmental archives such as peat bogs, sediments, corals, trees, polar ice, plant material from herbarium collections, and human tissue material have greatly helped to assess both ancient and recent atmospheric lead deposition and its sources on a regional and global scale. In Europe detectable atmospheric lead pollution began as early as 6000years ago due to enhanced soil dust and agricultural activities, as studies of peat bogs reveal. Increased lead emissions during ancient Greek and Roman times have been recorded and identified in many long-term archives such as lake sediments in Sweden, ice cores in Greenland, and peat bogs in Spain, Switzerland, the United Kingdom, and the Netherlands. For the period since the Industrial Revolution, other archives such as corals, trees, and herbarium collections provide similar chronologies of atmospheric lead pollution, with periods of enhanced lead deposition occurring at the turn of the century and since 1950. The main sources have been industry, including coal burning, ferrous and nonferrous smelting, and open waste incineration until c.1950 and leaded gasoline use since 1950. The greatest lead emissions to the atmosphere all over Europe occurred between 1950 and 1980 due to traffic exhaust. A marked drop in atmospheric lead fluxes found in most archives since the 1980s has been attributed to the phasing out of leaded gasoline. The isotope ratios of lead in the various archives show qualitatively similar temporal changes, for example, the immediate response to the introduction and phasing out of leaded gasoline. Isotope studies largely confirm source assessments based on lead emission inventories and allow the contributions of various anthropogenic sources to be calculated.

  15. Lead Poisoning

    Science.gov (United States)

    ... Topics Environment & Health Healthy Living Pollution Reduce, Reuse, Recycle Science – How It Works The Natural World Games ... OTHERS: Lead has recently been found in some plastic mini-blinds and vertical blinds which were made ...

  16. Identification of isotopically primitive interplanetary dust particles: A NanoSIMS isotopic imaging study

    Energy Technology Data Exchange (ETDEWEB)

    Floss, C; Stadermann, F J; Bradley, J P; Dai, Z R; Bajt, S; Graham, G; Lea, A S

    2005-09-02

    We have carried out a comprehensive survey of the isotopic compositions (H, B, C, N, O, S) of a suite of interplanetary dust particles (IDPs), including both cluster and individual particles. Isotopic imaging with the NanoSIMS shows the presence of numerous discrete hotspots that are strongly enriched in {sup 15}N, including the largest {sup 15}N enrichments ({approx}1300 {per_thousand}) observed in IDPs to date. A number of the IDPs also contain larger regions with more modest enrichments in {sup 15}N, leading to average bulk N isotopic compositions that are {sup 15}N-enriched in these IDPs. Although C isotopic compositions are normal in most of the IDPs, two {sup 15}N-rich N-hotspots have correlated {sup 13}C anomalies. CN{sup -}/C{sup -} ratios suggest that most of the {sup 15}N-rich hotspots are associated with relatively N-poor carbonaceous matter, although specific carriers have not been determined. H isotopic distributions are similar to those of N: D anomalies are present both as distinct very D-rich hotspots and as larger regions with more modest enrichments. Nevertheless, H and N isotopic anomalies are not directly correlated, consistent with results from previous studies. Oxygen isotopic imaging shows the presence of abundant presolar silicate grains in the IDPs. The O isotopic compositions of the grains are similar to those found in presolar oxide and silicate grains from primitive meteorites. Most of the silicate grains in the IDPs have isotopic ratios consistent with meteoritic Group 1 oxide grains, indicating origins in oxygen-rich red giant and asymptotic giant branch stars, but several presolar silicates exhibit the {sup 17}O and {sup 18}O enrichments of Group 4 oxide grains, whose origin is less well understood. Based on their N isotopic compositions, the IDPs studied here can be divided into two groups. One group is characterized as being ''isotopically primitive'' and consists of those IDPs that have anomalous bulk N isotopic

  17. Stable (206Pb, 207Pb, 208Pb) and radioactive (210Pb) lead isotopes in 1 year of growth of Sphagnum moss from four ombrotrophic bogs in southern Germany: Geochemical significance and environmental implications

    Science.gov (United States)

    Shotyk, William; Kempter, Heike; Krachler, Michael; Zaccone, Claudio

    2015-08-01

    The surfaces of Sphagnum carpets were marked with plastic mesh and 1 year later the production of plant matter was harvested in four ombrotrophic bogs from two regions of southern Germany: Upper Bavaria (Oberbayern, OB) and the Northern Black Forest (Nordschwarzwald, NBF). Radioactive, 210Pb was determined in solid samples using ultralow background gamma spectrometry while total Pb concentrations and stable isotopes (206Pb, 207Pb, 208Pb) were determined in acid digests using ICP-SMS. Up to 12 samples (40 × 40 cm) were collected per site, and 6-10 sites investigated per bog. The greatest variations within a given sampling site were in the range 212-532 Bq kg-1 for 210Pb activity, whereas 206Pb/207Pb and 208Pb/206Pb varied less than 1%. The median values of all parameters for the sites (6-10 per bog) were not significantly different. The median activities of 210Pb (Bq kg-1) in the mosses collected from the bogs in NBF (HO = 372 ± 56, n = 55; WI = 342 ± 58, n = 93) were slightly less from those in OB (GS = 394 ± 50, n = 55; KL = 425 ± 58, n = 24). However, the mosses in the NBF bogs exhibited much greater productivity (187-202 g m-2 a-1) compared to those of OB (71-91 g m-2 a-1), and this has a profound impact on the accumulation rates of 210Pb (Bq m-2 a-1), with the bogs in the NBF yielding fluxes (HO = 73 ± 30; WI = 65 ± 20) which are twice those of OB (GS = 29 ± 11; KL = 40 ± 13). Using the air concentrations of 210Pb measured at Schauinsland (SIL) in the southern Black Forest and average annual precipitation, the atmospheric fluxes of 210Pb at SIL (340 Bq m-2 a-1) exceeds the corresponding values obtained from the mosses by a factor of five, providing the first quantitative estimate of the net retention efficiency of 210Pb by Sphagnum. When the 210Pb activities of all moss samples are combined (n = 227), a significant decrease with increasing plant production rate is observed; in contrast, total Pb concentrations show the opposite trend. The contrasting

  18. Sulfur, Lead, Carbon and Oxygen Isotope Composition and Source of Ore-forming Materials of the Bangpu Pb-Zn Ore Deposit in Tibet%西藏邦铺铅锌矿床S、Pb、C、O同位素组成及成矿物质来源研究

    Institute of Scientific and Technical Information of China (English)

    王立强; 罗茂澄; 袁志洁; 陈伟; 冷秋锋; 张学全

    2012-01-01

    The Bangpu Pb-Zn deposit, formed in the periphery of the porphyry mineralization body of the ore district, is a skarn deposit with relatively rich ore grade, and the ore-forming elements are dominated by lead and zinc, without copper basically. Main metal sulfides were objects of this study, and S and Pb isotopic methods were used to investigate the source of the ore-forming minerals. The results show that the δ34S values of the ore metal sulfides have a wide distribution, and mainly vary in the range of -3.7‰-0.7‰, with the characteristics of tower distribution, and that these sulfur materials were mainly derived from the magma. Lead isotopes of the ore have stable composition and are positive common lead. The high μ values (larger than 9.58) of ore lead and the distribution characteristics of the data points in the evolution diagram of tectonic environment indicate that the ore lead was mainly derived from the upper crust. A comparison between this deposit and the nearby Zhibula and Jiama deposits shows that sulfur of these three deposits was exclusively derived from magma, and their metal materials show a certain regular pattern in source space, i.e., the contamination of crustal source material increased from south to north in the Qulong-Jiama-Bangpu ore district. Carbon and Oxygen isotope compositions of marble and calcite show that carbon in ore-forming fluid was mainly derived from the magma whereas the carbonate formation provided parts of other ore-forming materials.%邦铺铅锌矿床系邦铺钼铜矿区斑岩矿化体外围形成的矽卡岩型铅锌矿床;矿石品位较富,成矿元素以铅锌为主,基本不含铜.文章以矿床中主要金属硫化物为研究对象,采用S、Pb同位素研究方法对矿床成矿物质来源进行探讨.结果表明,矿石金属硫化物δ34S值分布范围较宽,但主要集中于-3.7‰~-0.7‰之问,具塔式分布特征,硫主要来源于岩浆;矿石铅同位素组成稳定,

  19. Rapid automated nuclear chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Meyer, R.A.

    1979-05-31

    Rapid Automated Nuclear Chemistry (RANC) can be thought of as the Z-separation of Neutron-rich Isotopes by Automated Methods. The range of RANC studies of fission and its products is large. In a sense, the studies can be categorized into various energy ranges from the highest where the fission process and particle emission are considered, to low energies where nuclear dynamics are being explored. This paper presents a table which gives examples of current research using RANC on fission and fission products. The remainder of this text is divided into three parts. The first contains a discussion of the chemical methods available for the fission product elements, the second describes the major techniques, and in the last section, examples of recent results are discussed as illustrations of the use of RANC.

  20. Rapid automated nuclear chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Meyer, R.A.

    1979-05-31

    Rapid Automated Nuclear Chemistry (RANC) can be thought of as the Z-separation of Neutron-rich Isotopes by Automated Methods. The range of RANC studies of fission and its products is large. In a sense, the studies can be categorized into various energy ranges from the highest where the fission process and particle emission are considered, to low energies where nuclear dynamics are being explored. This paper presents a table which gives examples of current research using RANC on fission and fission products. The remainder of this text is divided into three parts. The first contains a discussion of the chemical methods available for the fission product elements, the second describes the major techniques, and in the last section, examples of recent results are discussed as illustrations of the use of RANC.

  1. Redefining the utility of the three-isotope method

    Science.gov (United States)

    Cao, Xiaobin; Bao, Huiming

    2017-09-01

    The equilibrium isotope fractionation factor αeq is a fundamental parameter in the study of stable isotope effects. Experimentally, it has been difficult to establish that a system has attained equilibrium. The three-isotope method, using the initial trajectory of changing isotope ratios (e.g. 16O, 17O, and 18O) to deduce the final equilibrium point of isotope exchange, has long been hailed as the most rigorous experimental approach. However, over the years some researchers have cautioned on the limitations of this method, but the foundation of three-isotope method has not been properly examined and the method is still widely used in calibrating αeq for both traditional and increasingly non-traditional isotope systems today. Here, using water-water and dissolved CO2-water oxygen exchange as model systems, we conduct an isotopologues-specific kinetic analysis of the exchange processes and explore the underlying assumptions and validity of the three-isotope method. We demonstrate that without knowing the detailed exchange kinetics a priori the three-isotope method cannot lead to a reliable αeq. For a two-reservoir exchanging system, α determined by this method may be αeq, kinetic isotope effect, or apparent kinetic isotope effect, which can all bear different values. When multiple reservoirs exist during exchange, the evolving trajectory can be complex and hard to predict. Instead of being a tool for αeq determination, three-isotope method should be used as a tool for studying kinetic isotope effect, apparent kinetic isotope effect, and detailed exchange kinetics in diverse systems.

  2. Iron isotopes for the layered series of the Skaergaard intrusion

    Science.gov (United States)

    Lesher, C. E.; Lundstrom, C.; Brown, E.; Huang, F.; Glessner, J. J.; Hoffmann-Barfod, G.; Thy, P.

    2009-12-01

    It has long been held that magmatic evolution of the Skaergaard intrusion involved strong iron enrichment accompanying gabbro fractionation. Continued enrichment of iron in evolved liquids following FeTi oxide saturation is problematic and has been ascribed to a number of related factors, including 1) the composition of the Skaergaard parental magma, 2) changes in oxidation conditions and proportion of fractionating FeTi oxide and silicates during the course of differentiation, and 3) the effects of liquid immiscibility. In most differentiation scenarios differences in the partitioning of Fe+2 and Fe+3 between fractionating minerals and silicate melt are considered to be key to maintaining the bulk distribution coefficient for total iron below unity, thus permitting iron enrichment during magmatic evolution. Recent experimental work [1] predicts measureable fractionation of iron isotopes between magnetite and silicate melt that can lead to enrichment of isotopically lighter iron in derivative liquids compared to magnetite-rich cumulates. This possibility suggests that a signature of FeTi oxide fractionation may be recorded in the Fe isotope composition of Skaergaard gabbros. Initial investigation of this possibility is based on the analysis of 15 average gabbros from the layered series by high resolution MC-ICPMS after digestion