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Sample records for 206pb 204pb ratios

  1. Tracking atmospheric sulphur pollution from the study of Racomitrium lanuginosum mosses in Iceland: A multi-isotope approach (δ34S, 206Pb/204Pb, δ13C and δ15N)

    NASA Astrophysics Data System (ADS)

    Proust, E.; Widory, D.; Gautason, B.; Rogers, K.; Morrison, J.

    2010-12-01

    Among terrestrial plants, the applicability of mosses as monitoring organisms of atmospheric pollutants is a world-wide accepted technique due to their special biological and morphologic characteristics as nonvascular plants. They are commonly regarded as the best bioindicators of air quality because they can accumulate sulphur (S) and other elements to a far greater level than is necessary for their physiological needs. This study aims at using different isotope systematics δ34S, 206Pb/204Pb, δ13C and δ15N) to help understand the origin of S in the atmophsere of Reykjavik and its vicinity, and especially the potential contribution of surrounding geothermal plants. The selected Icelandic woolly fringe moss (Racomitrium lanuginosum (Hedw.) Brid.) is extremely common in lava fields and gravely and stony areas. Samples were taken in four distinct sampling sites around the city of Reykjavik: Bláfjöll area (south-eastern suburb of the city), and close to three power plants: Hellisheioarvirkjun (northern suburb of the city), Svartsengi (south-western suburb of the city) and Nesjavellir (north-eastern suburb of the city). Results show that, whatever the sampling context is, S is controlled by a binary mixing, between i) a high δ34S (around 16‰) end-member, characteristic of mosses from Hellisheioarvirkjun, and ii) a low δ34S (around -2‰) end-member, characteristic of mosses from Nesjavellir. The multi-isotope approach, confirms this binary relation and helps to constrain the different end-members involved.

  2. Lead isotope ratios in bone ash of blesbok (Damaliscus pygargus phillipsi): a means of screening for the accumulation of contaminants from uraniferous rocks.

    PubMed

    Nöthling, Johan O; Du Toit, Johannes S; Myburgh, Jan G

    2014-09-19

    This study was done to determine whether blesbok (Damaliscus pygargus phillipsi) from the Krugersdorp Game Reserve (KGR) in Gauteng Province, South Africa have higher concentrations of (238)U and higher (206)Pb/(204)Pb and (207)Pb/(204)Pb ratios in their bone ash than blesbok from a nearby control reserve that is not exposed to mine water and has no outcrops of uraniferous rocks. Eight blesbok females from the KGR and seven from the control site, all killed with a brain shot, were used. A Thermo X-series 2 quadrupole ICPMS was used to measure the concentrations of (238)U and lead and a Nu Instruments NuPlasma HR MC-ICP-MS to measure the lead isotope ratios in the tibial ash from each animal. KGR blesbok had higher mean concentrations of (238)U (P = 0.02) and ratios of (206)Pb/(204)Pb and (207)Pb/(204)Pb (P < 0.00001) than the control blesbok. The probability of rejecting the false null hypothesis of no difference in the (206)Pb/(204)Pb or (207)Pb/(204)Pb ratios between KGR and control reserve animals (the power of the test) was 0.999. The blesbok from the KGR accumulated contaminants from an uraniferous environment. The (206)Pb/(204)Pb and (207)Pb/(204)Pb ratios in tibial ash proved effective in confirming accumulation of contaminants from uraniferous rocks.

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

    NASA Astrophysics Data System (ADS)

    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.

  4. /sup 204/Pb(n,n'. gamma. )/sup 204/Pb reaction

    SciTech Connect

    Dawson, W.K.; Green, P.W.; Hooper, H.R.; Neilson, G.C.; Sheppard, D.M.; Siefken, H.E.; Smith, D.L.; Davidson, J.M.

    1980-08-01

    The excited states of /sup 204/Pb were studied using the /sup 204/Pb(n,n'..gamma..) reaction. Gamma-ray excitation functions and angular distributions were recorded using a small-sample technique. Previously unreported /sup 204/Pb levels were observed at 1605 +- 1, 1682 +- 1, 1762 +- 1, 1873 +- 1, and 2276 +- 3 keV excitation. The spins of the levels at 1682, 1762, 1873, and 2276 keV are J=1, 2, or 3/sup -/. The spin and parity of the 1605 keV level is limited to J/sup ..pi../=3/sup +/ or 4/sup +/. Multipole mixing ratios were measured for several transitions where the initial and final state spins and parities were firmly established from previous work.

  5. 26Al- 26Mg and 207Pb- 206Pb systematics of Allende CAIs: Canonical solar initial 26Al/ 27Al ratio reinstated

    NASA Astrophysics Data System (ADS)

    Jacobsen, Benjamin; Yin, Qing-zhu; Moynier, Frederic; Amelin, Yuri; Krot, Alexander N.; Nagashima, Kazuhide; Hutcheon, Ian D.; Palme, Herbert

    2008-07-01

    The precise knowledge of the initial 26Al/ 27Al ratio [( 26Al/ 27Al) 0] is crucial if we are to use the very first solid objects formed in our Solar System, calcium-aluminum-rich inclusions (CAIs) as the "time zero" age-anchor and guide future work with other short-lived radio-chronometers in the early Solar System, as well as determining the inventory of heat budgets from radioactivities for early planetary differentiation. New high-precision multi-collector inductively-coupled plasma mass spectrometry (MC-ICP-MS) measurements of 27Al/ 24Mg ratios and Mg-isotopic compositions of nine whole-rock CAIs (six mineralogically characterized fragments and three micro-drilled inclusions) from the CV carbonaceous chondrite, Allende yield a well-defined 26Al- 26Mg fossil isochron with an ( 26Al/ 27Al) 0 of (5.23 ± 0.13) × 10 - 5 . Internal mineral isochrons obtained for three of these CAIs ( A44A, AJEF, and A43) are consistent with the whole-rock CAI isochron. The mineral isochron of AJEF with ( 26Al/ 27Al) 0 = (4.96 ± 0.25) × 10 - 5 , anchored to our precisely determined absolute 207Pb- 206Pb age of 4567.60 ± 0.36 Ma for the same mineral separates, reinstate the "canonical" ( 26Al/ 27Al) 0 of 5 × 10 - 5 for the early Solar System. The uncertainty in ( 26Al/ 27Al) 0 corresponds to a maximum time span of ± 20 Ka (thousand years), suggesting that the Allende CAI formation events were culminated within this time span. Although all Allende CAIs studied experienced multistage formation history, including melting and evaporation in the solar nebula and post-crystallization alteration likely on the asteroidal parent body, the 26Al- 26Mg and U-Pb-isotopic systematics of the mineral separates and bulk CAIs behaved largely as closed-system since their formation. Our data do not support the "supra-canonical" 26Al/ 27Al ratio of individual minerals or their mixtures in CV CAIs, suggesting that the supra-canonical 26Al/ 27Al ratio in the CV CAIs may have resulted from post

  6. The application of lead isotope ratios in the Antarctic macroalga Iridaea cordata as a contaminant monitoring tool.

    PubMed

    Runcie, John W; Townsend, Ashley T; Seen, Andrew J

    2009-07-01

    Lead (Pb) isotope ratios were measured in the marine macroalga Iridaea cordata collected from four locations in the Windmill Islands, East Antarctica. Based on the masses of thalli collected, samples analysed in this study were likely to be a mixture of one and two year old thalli. For a sample of thalli of various ages (<12 months to 2 years old) from the same site there was no apparent variation in Pb concentration or Pb isotope ratio with thallus mass/age, indicating that contaminant sources had been constant over the lifetime of the thalli sampled. I.cordata samples close to the Thala Valley waste disposal site (Brown Bay Inner) near the Australian Station, Casey, displayed isotopic signatures ((208)Pb/(204)Pb 35.99; (206)Pb/(207)Pb 1.066; n=3; average values shown) trending towards that possessed by major Australian Pb sources (Broken Hill and Mt Isa, (208)Pb/(204)Pb 35.60; (206)Pb/(207)Pb 1.041) suggesting that these samples had been exposed to anthropogenic Pb originating from the Thala Valley waste disposal site. Material collected hundreds of metres from the tip location at Brown Bay Outer had isotopic values ((208)Pb/(204)Pb 36.32; (206)Pb/(207)Pb 1.088; n=10) intermediate between Brown Bay Inner and sites further from the contaminant source at Sparkes Bay and Wilkes ((208)Pb/(204)Pb 36.46; (206)Pb/(207)Pb 1.094; n=4) showing that contaminant transport was predominantly restricted to Brown Bay Inner. This study demonstrates that the isotope ratios of Pb in marine macroalgae can provide valuable information as to the origin and extent of heavy metal flux in a marine environment.

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

    PubMed

    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 (p<0.05) positive correlations for (206)Pb/(204)Pb and (206)Pb/(207)Pb, and a significant negative correlation for (208)Pb/(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.

  8. Time differences in the formation of meteorites as determined from the ratio of lead-207 to lead-206

    USGS Publications Warehouse

    Tatsumoto, M.; Knight, R.J.; Allegre, C.J.

    1973-01-01

    Measurements of the lead isotopic composition and the uranium, thorium, and lead concentrations in meteorites were made in order to obtain more precise radiometric ages of these members of the solar system. The newly determined value of the lead isotopic composition of Canyon Diablo troilite is as follows: 206Pb/204Pb = 9.307, 207Pb/204Pb = 10.294, and 208Pb/204Pb = 29.476. The leads of Angra dos Reis, Sioux County, and Nuevo Laredo achondrites are very radiogenic, the 206Pb/204Pb values are about 200, and the uranium-thorium-lead systems are nearly concordant. The ages of the meteorites as calculated from a single-stage 207Pb/206Pb isochron based on the newly determined primordial lead value and the newly reported 235U and 238U decay constants, are 4.528 ?? 10 9 years for Sioux County and Nuevo Laredo and 4.555 ?? 10 9 years for Angra dos Reis. When calculated with the uranium decay constants used by Patterson, these ages are 4.593 ?? 109 years and 4.620 ?? 109 years, respectively, and are therefore 40 to 70 ?? 106 years older than the 4.55 ?? 109 years age Patterson reported. The age difference of 27 ?? 106 years between Angra dos Reis and the other two meteorites is compatible with the difference between the initial 87Sr/86Sr ratio of Angra dos Reis and that of seven basaltic achondrites observed by Papanastassiou and Wasserburg. The time difference is also comparable to that determined by 129I-129Xe chronology. The ages of ordinary chondrites (H5 and L6) range from 4.52 to 4.57 ?? 109 years, and, here too, time differences in the formation of the parent bodies or later metamorphic events are indicated. Carbonaceous chondrites (C2 and C3) appear to contain younger lead components.

  9. 206Pb-230Th-234U-238U and 207Pb-235U geochronology of Quaternary opal, Yucca Mountain, Nevada

    USGS Publications Warehouse

    Neymark, Leonid A.; Amelin, Yuri V.; Paces, James B.

    2000-01-01

    U–Th–Pb isotopic systems have been studied in submillimeter-thick outermost layers of Quaternary opal occurring in calcite–silica fracture and cavity coatings within Tertiary tuffs at Yucca Mountain, Nevada, USA. These coatings preserve a record of paleohydrologic conditions at this site, which is being evaluated as a potential high-level nuclear waste repository. The opal precipitated from groundwater is variably enriched in 234U (measured 234U/238U activity ratio 1.124–6.179) and has high U (30–313 ppm), low Th (0.008–3.7 ppm), and low common Pb concentrations (measured 206Pb/204Pb up to 11,370). It has been demonstrated that the laboratory acid treatment used in this study to clean sample surfaces and to remove adherent calcite, did not disturb U–Th–Pb isotopic systems in opal. The opal ages calculated from 206Pb∗/238U and 207Pb∗/235U ratios display strong reverse discordance because of excess radiogenic 206Pb∗ derived from the elevated initial 234U. The data are best interpreted using projections of a new four-dimensional concordia diagram defined by 206Pb∗/238U, 207Pb∗/235U, 234U/238Uactivity, and 230Th/238Uactivity. Ages and initial 234U/238U activity ratios have been calculated using different projections of this diagram and tested for concordance. The data are discordant, that is observed 207Pb∗/235U ages of 170 ± 32 (2σ) to 1772 ± 40 ka are systematically older than 230Th/U ages of 34.1 ± 0.6 to 452 ± 32 ka. The age discordance is not a result of migration of uranium and its decay products under the open system conditions, but a consequence of noninstantaneous growth of opal. Combined U–Pb and 230Th/U ages support the model of slow mineral deposition at the rates of millimeters per million years resulting in layering on a scale too fine for mechanical sampling. In this case, U–Pb ages provide more accurate estimates of the average age for mixed multiage samples than 230Th/U ages, because ages based on shorter

  10. Measurement of internal pairs from {sup 206}Pb

    SciTech Connect

    Ahmad, I.; Back, B.B.; Betts, R.R.

    1995-08-01

    The failure to observe sharp sum-energy lines in measurements of {sup 238}U + {sup 181}Ta and {sup 238}U + {sup 232}Th raises the issue of the correct functioning of APEX under in-beam conditions. Extensive measurements with electron and pair emitting sources were used to demonstrate the resolution and acceptance of APEX, but the possibility remains that some unforeseen background or other effects might compromise the ability to see peaks in-beam. In order to test the functioning of APEX under the most stringent conditions, we also performed a measurement of internal pairs produced in the decay of the 2.648-MeV 3{sup -} state in {sup 206}Pb to the 2{sup +} state at 0.803 MeV. The 3{sup -} state was excited in the {sup 206}Pb + {sup 206}Pb reaction at 5.9 MeV/u with a cross section of roughly 40 mb, resulting in an expected pair cross section of approximately 16 {mu}b. It should be emphasized that this measurement represents a much stricter test of the functioning of the apparatus than the observation of sum-energy lines would represent, as the internal pair measurement requires a Doppler shift correction before the transition can be seen. These data were analyzed and clearly show the expected peak. A Doppler-corrected sum-energy spectrum showing the expected IPC line at 823 keV. At present we are evaluating the acceptance of APEX for events of this type but it is clear that the observed yield is close to expectations.

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

    PubMed

    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.

  12. A Single Grain U-Pb and Pb-Pb Dating and D/H Ratios of the Phosphate Mineral in ALH84001

    NASA Astrophysics Data System (ADS)

    Koike, M.; Ota, Y.; Takahata, N.; Sano, Y.; Sugiura, N.

    2012-12-01

    There are many studies that determine U-Pb and Pb-Pb ages of phosphates in Martian meteorites. Phosphate minerals such as an apatite (Ca5(PO4)3[OH, F, Cl]) and a whitlockite (Ca9 [Mg, Fe2+] (PO4)6 PO3OH) contain water in the form of OH, which provides us hydrogen isotopic information. The goal of this study is to obtain a crystallization age and hydrogen isotopic distributions of each grain and to relate them to the surface evolution of Mars. ALH84001 is known to be about 4 billion years old [1]. Its carbonates and maskelynite showed high D/H ratios with large deviations, which indicates large fractionation at early Mars surface [2]. Due to small grain sizes and limited spatial resolutions of measurements, previous studies used several grains for one age or one series of isotopic distributions. Here we determined single grain ages and D/H ratios using NanoSIMS with a high spatial resolution. A thin section of ALH84001 was polished and carbon-coated. The section was then observed by SEM-EDS to locate phosphate minerals. A large phosphate grain (>100μm) was found and analyzed by NanoSIMS. A ~10nA O- primary ion beam (with spot diameter of ~20μm) was used for U-Pb and Pb-Pb measurements and a ~1nA (spot diameter of <10μm) was for D/H ratio measurements. An apatite from a Prairie Lake circular complex, PRAP, with a known age (1156 Ma; [3]) was used as a standard for U-Pb. The D/H ratio and the water content of an apatite from Morocco were measured by conventional methods to use as a D/H standard. 238U-206Pb isochron, 207Pb-206Pb isochron, and total U-Pb isochron age, a regression line in 3-D space (238U/206Pb-207Pb/206Pb-204Pb/206Pb) showed a consistent age ~4 Ga. The ages obtained in this study were also consistent with previous U-Pb dating within experimental errors. D/H ratios in the same grain showed high values and a considerable deviation, which seems to be due to mixing of terrestrial water. References: [1] Terada K. et al. 2003 Meteoritics & Planet. Sci. 38

  13. Solution of controversy over 1583-keV levels in sup 204 Pb

    SciTech Connect

    Trzaska, W.H.; Julin, R.; Kantele, J.; Kumpulainen, J. )

    1989-09-01

    Data from {sup 204}Pb({ital p},{ital p}{prime}){sup 204}Pb conversion-electron and gamma-ray experiments, together with previous results, prove the existence of two levels (0{sup +} and 2{sup +}) at 1583-keV excitation energy in {sup 204}Pb. Modified values (limits) of the {rho}{sub 21}{sup 2} and {ital X}{sub 211} are 0.0013{lt}{rho}{sub 21}{sup 2}{lt}0.015 and {ital X}{sub 211}{gt}0.073. New experimental evidence indicates that all the three observed excited {ital O}{sup +} states in {sup 204}Pb can be explained as belonging to the four-neutron-hole valence space and, therefore, there is no clear candidate for the proton 2p-2h intruder state in this nucleus.

  14. The graphical presentation of lead isotope data for environmental source apportionment.

    PubMed

    Ellam, R M

    2010-07-15

    Lead isotope ratios are widely used to identify original sources of Pb in the environment. Such source apportionment depends on the ability to distinguish potential sources on the basis of their isotopic composition. However, almost all terrestrial Pb is co-linear in some of the plots i.e. (206)Pb/(208)Pb versus (206)Pb/(207)Pb and (206)Pb/(204)Pb versus (206)Pb/(207)Pb commonly presented in the literature. These diagrams are unable to distinguish more than two sources of environmental Pb. Linear trends in such plots are an inevitable consequence of the co-linearity of terrestrial leads and should not be taken necessarily to indicate simple binary mixing of sources. A more reliable test for multiple source mixing can be obtained from plots involving (206)Pb/(204)Pb, (207)Pb/(204)Pb and (208)Pb/(204)Pb and therefore requires measurements of the minor (204)Pb isotope.

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

    SciTech Connect

    Smith, D.R. Univ. of California, Santa Cruz, CA ); Markowitz, M.E.; Rosen, J.F. ); Crick, J.; Flegal, A.R. )

    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.

  16. Chemical signatures of the Anthropocene in the Clyde estuary, UK: sediment-hosted Pb, (207/206)Pb, total petroleum hydrocarbon, polyaromatic hydrocarbon and polychlorinated biphenyl pollution records.

    PubMed

    Vane, C H; Chenery, S R; Harrison, I; Kim, A W; Moss-Hayes, V; Jones, D G

    2011-03-13

    The sediment concentrations of total petroleum hydrocarbons (TPHs), polyaromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), Pb and (207/206)Pb isotope ratios were measured in seven cores from the middle Clyde estuary (Scotland, UK) with an aim of tracking the late Anthropocene. Concentrations of TPHs ranged from 34 to 4386 mg kg(-1), total PAHs from 19 to 16,163 μg kg(-1) and total PCBs between less than 4.3 to 1217 μg kg(-1). Inventories, distributions and isomeric ratios of the organic pollutants were used to reconstruct pollutant histories. Pre-Industrial Revolution and modern non-polluted sediments were characterized by low TPH and PAH values as well as high relative abundance of biogenic-sourced phenanthrene and naphthalene. The increasing industrialization of the Clyde gave rise to elevated PAH concentrations and PAH isomeric ratios characteristic of both grass/wood/coal and petroleum and combustion (specifically petroleum combustion). Overall, PAHs had the longest history of any of the organic contaminants. Increasing TPH concentrations and a concomitant decline in PAHs mirrored the lessening of coal use and increasing reliance on petroleum fuels from about the 1950s. Thereafter, declining hydrocarbon pollution was followed by the onset (1950s), peak (1965-1977) and decline (post-1980s) in total PCB concentrations. Lead concentrations ranged from 6 to 631 mg kg(-1), while (207/206)Pb isotope ratios spanned 0.838-0.876, indicative of various proportions of 'background', British ore/coal and Broken Hill type petrol/industrial lead. A chronology was established using published Pb isotope data for aerosol-derived Pb and applied to the cores.

  17. Deep Sub-Barrier Fusion Enhancement in the {sup 6}He+{sup 206}Pb Reaction

    SciTech Connect

    Penionzhkevich, Yu.E.; Zagrebaev, V.I.; Lukyanov, S.M.; Kalpakchieva, R.

    2006-04-28

    The fusion of {sup 6}He with {sup 206}Pb has been studied at energies close to and below the Coulomb barrier. The experiment was carried out at the Dubna Radioactive Ion Beams complex of FLNR, JINR. The {sup 6}He beam intensity was about 5x10{sup 6} pps, the maximum energy being 60.3{+-}0.4 MeV. The yield of the {sup 210}Po isotope, produced in the 2n-evaporation channel, demonstrates an extremely large enhancement of the sub-barrier fusion cross section as compared with the {sup 4}He+{sup 208}Pb reaction. This enhancement is most likely due to the mechanism of 'sequential fusion' with an intermediate neutron transfer from {sup 6}He to the Pb nucleus with positive Q values.

  18. Final report of the key comparison CCQM-K98: Pb isotope amount ratios in bronze

    NASA Astrophysics Data System (ADS)

    Vogl, Jochen; Yim, Yong-Hyeon; Lee, Kyoung-Seok; Goenaga-Infante, Heidi; Malinowskiy, Dmitriy; Ren, Tongxiang; Wang, Jun; Vocke, Robert D., Jr.; Murphy, Karen; Nonose, Naoko; Rienitz, Olaf; Noordmann, Janine; Näykki, Teemu; Sara-Aho, Timo; Ari, Betül; Cankur, Oktay

    2014-01-01

    Isotope amount ratios are proving useful in an ever increasing array of applications that range from studies unravelling transport processes, to pinpointing the provenance of specific samples as well as trace element quantification by using isotope dilution mass spectrometry (IDMS). These expanding applications encompass fields as diverse as archaeology, food chemistry, forensic science, geochemistry, medicine and metrology. However, to be effective tools, the isotope ratio data must be reliable and traceable to enable the comparability of measurement results. The importance of traceability and comparability in isotope ratio analysis has already been recognized by the Inorganic Analysis Working Group (IAWG) within the CCQM. While the requirements for isotope ratio accuracy and precision in the case of IDMS are generally quite modest, 'absolute' Pb isotope ratio measurements for geochemical applications as well as forensic provenance studies require Pb isotope ratio measurements of the highest quality. To support present and future CMCs on isotope ratio determinations, a key comparison was urgently needed and therefore initiated at the IAWG meeting in Paris in April 2011. The analytical task within such a comparison was decided to be the measurement of Pb isotope amount ratios in water and bronze. Measuring Pb isotope amount ratios in an aqueous Pb solution tested the ability of analysts to correct for any instrumental effects on the measured ratios, while the measurement of Pb isotope amount ratios in a metal matrix sample provided a real world test of the whole chemical and instrumental procedure. A suitable bronze material with a Pb mass fraction between 10 and 100 mg•kg-1 and a high purity solution of Pb with a mass fraction of approximately 100 mg•kg-1 was available at the pilot laboratory (BAM), both offering a natural-like Pb isotopic composition. The mandatory measurands, the isotope amount ratios n(206Pb)/n(204Pb), n(207Pb)/n(204Pb) and n(208Pb)/n(204Pb

  19. Old Masters' lead white pigments: investigations of paintings from the 16th to the 17th century using high precision lead isotope abundance ratios.

    PubMed

    Fortunato, G; Ritter, A; Fabian, D

    2005-06-01

    White lead (2PbCO(3).Pb(OH)(2)), a common component in 17c. artists' painting materials, was singled out to investigate the potential of lead isotope abundance ratios in the field of authentication and origin assignment. Paintings by Peter Paul Rubens, Anthony van Dyck and other Old Masters of the Northern and Southern schools were chosen for this study. An interdisciplinary approach was chosen using both analytical instrumental methods, art technological and art historical knowledge. Minute samples taken from paintings from selected art collections worldwide were investigated using mass spectrometry, scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). The high precision lead isotope abundance ratios were measured by multiple collector inductively coupled plasma mass spectrometry (MC-ICP-MS). The determination of the calcium matrix influence with respect to possible bias effects to the isotope ratios gave clear decision support, to whether a result lies within the stated combined measurement uncertainty of the result, to eliminate time-consuming matrix separations. The scatter plots of the measured isotope abundance ratios for the painting pigments from P. P. Rubens, A. van Dyck and other Flemish painters exhibit a very narrow distribution forming a cluster. The range of the measured ratio (206)Pb/(204)Pb amounts to 0.55% and for the ratio (207)Pb/(204)Pb to 0.2%. The comparison of the data to cis-alpine (Italian) sample pigments from paintings from the same time period reveals a clear distinction between the two fields. With respect to the lead isotope data originating from the ores it is assumed that the pigment isotope ratio distribution can be explained by very distinct origin of raw materials. Presumably, no mixing of different lead ores from Europe took place. The comparison of the measured white lead isotope ratio values (Flemish paintings) and the data from ore samples led to the unexpected conclusion that local ores were not

  20. Plumbotectonic aspects of polymetallic vein mineralization in Paleozoic sediments and Proterozoic basement of Moravia (Czech Republic)

    NASA Astrophysics Data System (ADS)

    Slobodník, Marek; Jacher-Śliwczyńska, Katarzyna; Taylor, Matthew C.; Schneider, Jens; Dolníček, Zdeněk

    2008-02-01

    A regional isotopic study of Pb and S in hydrothermal galenas and U-Pb and S in potential source rocks was carried out for part of Moravia, Czech Republic. Two major generations of veins, (syn-) Variscan and post-Variscan, are defined based on the Pb-isotope system together with structural constraints (local structures and regional trends). The Pb-isotopic compositions of galena plot in two distinct populations with outliers in 206Pb/204Pb-207Pb/204Pb space. Galena from veins hosted in greywackes provides a cluster with the lowest Pb-Pb ratios: 206Pb/204Pb = 18.15-18.27, 207Pb/204Pb = 15.59-15.61, 208Pb/204Pb = 38.11-38.23. Those hosted in both limestones and greywackes provide the second cluster: 206Pb/204Pb = 18.37-18.44, 207Pb/204Pb = 15.60-15.63, 208Pb/204Pb = 38.14-38.32. These clusters suggest model Pb ages as Early Carboniferous and Triassic-Jurassic, the latter associated with MVT-like deposits. Two samples from veins hosted in Proterozoic rocks lie outside the two clusters: in metagranitoid (206Pb/204Pb = 18.55, 207Pb/204Pb = 15.64, 208Pb/204Pb = 38.29) and in orthogneiss (206Pb/204Pb = 18.79, 207Pb/204Pb = 15.73, 208Pb/204Pb = 38.54). The results from these two samples suggest an interaction of mineralizing fluids with the radiogenic Pb-rich source (basement?). The values of δ34S suggest the Paleozoic host rocks (mostly -6.7 to +5.2‰ CDT) as the source of S for hydrothermal sulfides (mostly -4.8 to +2.5‰ CDT). U-Pb data and Pb isotope evolutionary curves indicate that Late Devonian and Early Carboniferous sediments, especially siliciclastics, are the general dominant contributor of Pb for galena mineralization developed in sedimentary rocks. Plumbotectonic mixing occurred, it is deduced, only between the lower and the upper crust (the latter involving Proterozoic basement containing heterogeneous radiogenic Pb), without any significant input from the mantle. It is concluded that in the Moravo-Silesian and Rhenohercynian zones (including proximal

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

    PubMed

    Conkova, M; Kubiznakova, J

    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 microg g(-1)) reflected air pollution in the city of Prague. The lowest Pb content (0.3-2.6 microg g(-1)) was found at the Kosetice EMEP "background pollution" site. Changes in (206)Pb/(207)Pb and (208)Pb/(206)Pb isotope ratios were in agreement with operation times of the Czech main anthropogenic Pb sources. Shortly after the Second World War, the (206)Pb/(207)Pb isotope ratio in bark pockets decreased from 1.17 to 1.14 and the (208)Pb/(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 ((206)Pb/(207)Pb of 1.11) lead to lower (206)Pb/(207)Pb in bark pockets over time. High-radiogenic lignite-derived Pb ((206)Pb/(207)Pb of 1.18 to 1.19) was detected in areas affected by coal combustion rather than by traffic.

  2. Lead isotopic composition of insoluble particles from widespread mountain glaciers in western China: Natural vs. anthropogenic sources

    NASA Astrophysics Data System (ADS)

    Yu, Guangming; Xu, Jianzhong; Kang, Shichang; Zhang, Qianggong; Huang, Jie; Ren, Qian; Ren, Jiawen; Qin, Dahe

    2013-08-01

    Stable lead (Pb) isotopic fingerprints provide opportunities to trace natural and anthropogenic Pb sources in the environment. In order to evaluate Pb deposition from different sources over mountainous areas of western China, Pb isotopic compositions were characterized from modern aeolian dust in 15 snowpit samples collected from 13 typical mountain glaciers between 2008 and 2010. Most of the snowpits sampled cover more than a whole year of accumulation and overlap with each other on deposition date. Pb isotopic variability among all the samples is small, varying in the range of 18.1399-18.9199 for 206Pb/204Pb, 15.5979-15.8743 for 207Pb/204Pb, 38.2272-39.9453 for 208Pb/204Pb, 1.1605-1.2009 for 206Pb/207Pb and 2.4433-2.5182 for 208Pb/207Pb. Three isotopic plots of the different Pb isotope ratios (207Pb/204Pb vs. 206Pb/204Pb, 208Pb/204Pb vs. 206Pb/204Pb, and 208Pb/207Pb vs. 206Pb/207Pb) in all the samples show identical geographic trends, with more radiogenic in the south and less in the north. This trend is consistent with the distribution of natural dust sources and supports the interpretation of a regional/local source for insoluble particles (IP) to snow/glaciers in this region. Comparison with the Pb isotope results from potential dust sources, however, it shows that the Pb isotopic compositions of IP samples in snow samples are relatively less radiogenic. Parts of these less-radiogenic Pb isotopes are comparable with the ice core results during recent decades, which are shown to be influenced by anthropogenic sources. At sites located along the periphery of western China, the Pb isotopic compositions are much closer to anthropogenic results. Natural and anthropogenic Pb sources are roughly assessed using a simple binary model. The sites with a high anthropogenic fraction are at lower elevations and are relatively close to population centers.

  3. Direct determination of lead isotopes (206Pb, 207Pb, 208Pb) in arctic ice samples at picogram per gram levels using inductively coupled plasma-sector field MS coupled with a high-efficiency sample introduction system.

    PubMed

    Krachler, Michael; Zheng, James; Fisher, David; Shotyk, William

    2004-09-15

    Adopting strict cleanroom procedures, ice samples from the Canadian High Arctic have been analyzed for Pb concentrations and Pb isotopes (206Pb, 207Pb, 208Pb) using ICP-SMS. The detection limit for Pb (0.06 pg g(-1)) was approximately 2 orders of magnitude lower than the lowest concentration of Pb in the ice samples (range, 4.3-1660 pg g(-1); median, 45 pg g(-1)). Acidification of ice samples with high-purity HNO3 for stabilization purposes contributed only 0.004 pg of Pb g(-1), which is an insignificant source of Pb. Using a new sample introduction system consisting of a heated (140 degrees C) minicyclonic spray chamber and a Peltier cooled condenser (2 degrees C) and by replacing the conventional sample cone with a high-performance cone, signal intensities for Pb were increased by approximately 1 order of magnitude. Thus, it was possible not only to measure Pb isotope ratios directly using ICP-SMS but also to achieve reasonable precision (approximately 0.2%) at low picogram per gram concentrations of total Pb. This precision is comparable to that achievable by thermal ionization mass spectrometry at such low Pb concentrations, but the ICP-SMS requires much less sample volume (approximately 2 mL), needs no sample pretreatment, and therefore is considerably faster and less expensive than the conventional approach. Even though absolute Pb concentrations in two ice samples dating from 1974 and 1852 were very similar (9 and 6 pg g(-1)) their fundamentally different isotopic signature (206Pb/207Pb: 1.169 +/- 0.002 vs 1.147 +/- 0.003) clearly indicates different sources of Pb. The analytical procedures described here, therefore, offer great promise for fingerprinting the predominant sources of atmospheric Pb in polar snow and ice.

  4. 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

    NASA Astrophysics Data System (ADS)

    Shotyk, William; Kempter, Heike; Krachler, Michael; Zaccone, Claudio

    2015-08-01

    behaviour of 210Pb and total Pb in the mosses may reflect differences in the particle size distribution of the corresponding aerosols, their physical and chemical properties, the extent of their interaction with plant surfaces, or some combination of these factors. The 206Pb/207Pb ratios from NBF (HO = 1.159 ± 0.002, n = 19; WI = 1.157 ± 0.003, n = 48) and OB (GS = 1.157 ± 0.003, n = 28; KL = 1.159 ± 0.003, n = 15) are uniform and indicate that both regions are impacted by Pb from predominately anthropogenic sources. Although Sphagnum moss represents an established receptor in monitoring atmospheric Pb deposition, the physical characteristics (size, morphology, composition) of the three predominant kinds of Pb-bearing aerosols considered here, namely 210Pb (adsorbed onto aerosol surfaces, following decay of 222Rn), anthropogenic Pb (sub-micron aerosols from high temperature combustion processes) and lithogenic Pb soil-derived mineral dusts (tens of microns, from chemical weathering of crustal rocks), are fundamentally different and these have consequences for the retention efficiency of the three kinds of particles.

  5. Feather lead concentrations and207Pb/206Pb ratios reveal lead exposure history of California condors (Gymnogyps californianus)

    USGS Publications Warehouse

    Finkelstein, M.E.; George, D.; Scherbinski, S.; Gwiazda, R.; Johnson, M.; Burnett, J.; Brandt, J.; Lawrey, S.; Pessier, Allan P.; Clark, M.; Wynne, J.; Grantham, And J.; Smith, D.R.

    2010-01-01

    Lead poisoning is a primary factor impeding the survival and recovery of the critically endangered California Condor (Gymnogyps californianus). However, the frequency and magnitude of lead exposure in condors is not well-known in part because most blood lead monitoring occurs biannually, and biannual blood samples capture only ???10% of a bird's annual exposure history. We investigated the use of growing feathers from free-flying condors in California to establish a bird's lead exposure history. We show that lead concentration and stable lead isotopic composition analyses of sequential feather sections and concurrently collected blood samples provided a comprehensive history of lead exposure over the 2-4 month period of feather growth. Feather analyses identified exposure events not evident from blood monitoring efforts, and by fitting an empirically derived timeline to actively growing feathers, we were able to estimate the time frame for specific lead exposure events. Our results demonstrate the utility of using sequentially sampled feathers to reconstruct lead exposure history. Since exposure risk in individuals is one determinant ?? 2010 American Chemical Society.

  6. Feather lead concentrations and (207)Pb/(206)Pb ratios reveal lead exposure history of California Condors (Gymnogyps californianus).

    PubMed

    Finkelstein, M E; George, D; Scherbinski, S; Gwiazda, R; Johnson, M; Burnett, J; Brandt, J; Lawrey, S; Pessier, A P; Clark, M; Wynne, J; Grantham, J; Smith, D R

    2010-04-01

    Lead poisoning is a primary factor impeding the survival and recovery of the critically endangered California Condor (Gymnogyps californianus). However, the frequency and magnitude of lead exposure in condors is not well-known in part because most blood lead monitoring occurs biannually, and biannual blood samples capture only approximately 10% of a bird's annual exposure history. We investigated the use of growing feathers from free-flying condors in California to establish a bird's lead exposure history. We show that lead concentration and stable lead isotopic composition analyses of sequential feather sections and concurrently collected blood samples provided a comprehensive history of lead exposure over the 2-4 month period of feather growth. Feather analyses identified exposure events not evident from blood monitoring efforts, and by fitting an empirically derived timeline to actively growing feathers, we were able to estimate the time frame for specific lead exposure events. Our results demonstrate the utility of using sequentially sampled feathers to reconstruct lead exposure history. Since exposure risk in individuals is one determinant of population health, our findings should increase the understanding of population-level effects from lead poisoning in condors; this information may also be helpful for other avian species potentially impacted by lead poisoning. PMID:20199067

  7. U-Th-Pb isotopic constraints on the oxidation age of 3.4 Ga basalts from Marble Bar, Pilbara Craton, NW Australia

    NASA Astrophysics Data System (ADS)

    Li, W.; Johnson, C.; Beard, B. L.

    2011-12-01

    Determining the evolution of Earth's early atmosphere is critical to understanding the geologic history of the Earth, and one of the key aspects of atmospheric evolution has been the development of free oxygen. A common model involves an increase in free O2 between 2.4 and 2.2 Ga, termed the Great Oxidation Event (GOE). Although there is growing evidence for free O2 in the atmosphere or photic zone of the oceans several hundred m.y. before the GOE, hematite alteration products in 3.4 Ga basalts from the Marble Bar area of the Pilbara Craton, NW Australia have been used to infer the presence of an O2-bearing atmosphere even earlier. These Fe-oxides have not been directly dated, however, raising the possibility that they formed at a later time. Here we report new U-Th-Pb isotopic results of Apex Basalt samples from the ABDP-1 drill core at Marble Bar that allows determination of the age of the iron oxides. The basalt samples that have been variously oxidized have highly variable Pb and U concentrations, and scatter about a 207Pb/204Pb-206Pb/204Pb array that could be interpreted as an Archean age. U/Pb ratios are positively correlated with Fe(III)/ Fetotal ratios, indicating that U enrichment accompanied oxidation. In contrast, Th is positively correlated with Zr, suggesting Th has been immobile. The samples do not form isochrons on 238U/204Pb-206Pb/204Pb, 235U/204Pb-207Pb/204Pb, or 232Th/204Pb-208Pb/204Pb diagrams, indicating post-formation U and Pb addition. The 207Pb/204Pb-206Pb/204Pb array, therefore, is a mixing line and not an isochron. The U-Pb isotope data mandate that the age for U addition for three basalt samples must be younger than 2.5 Ga, even in the most conservative estimate. A more stringent model, which compares the measured U/Th ratios with those required to produce the 208Pb/204Pb-206Pb/204Pb variations, indicates that U enrichment most likely occurred in the last 200 m.y. This relatively young age for U enrichment is consistent with the deep

  8. Lead-isotopic compositions of diverse igneous rocks and ore deposits from southwestern New Mexico and their implications for early Proterozoic crustal evolution in the western United States.

    USGS Publications Warehouse

    Stacey, J.S.; Hedlund, D.C.

    1983-01-01

    Basement rocks in this area are 1750 m.y. old and extend northward through Colorado to Utah. Galena data show that the fraction of older sialic lead in these rocks increases toward the the Archaean craton in Wyoming. The crust apparently developed southward from Wyoming in stages at 2400 m.y. ago or before, 2100 m.y. ago and 1750 m.y. ago. The Laramide alkali to calc-alkaline rocks and their associated porphyry Cu and massive replacement deposits have similar 206Pb/204Pb ratios and are the least radiogenic in the region; their 206Pb/204Pb ratios are all 18.0. Pb isotopes in this region offer some criteria for prospecting purposes. The 206Pb/204Pb values for the larger ore deposits related to Laramide activity are all <18.0, particularly for the larger ones. Within the mid- Tertiary group, the same criteria apply - i.e. the largest deposits have the lowest 206Pb/204Pb ratios. -L.C.H.

  9. U-Th-Pb isotope data indicate phanerozoic age for oxidation of the 3.4 Ga Apex Basalt

    NASA Astrophysics Data System (ADS)

    Li, Weiqiang; Johnson, Clark M.; Beard, Brian L.

    2012-02-01

    The occurrence of ferric oxides in Archean rocks has played an important role in discussions on the amount of free oxygen in the atmosphere of the ancient Earth. Recognizing that post-Archean weathering may also produce oxide minerals, drill cores have been used to obtain samples beneath the depth of Phanerozoic weathering. The first core of the Archean Biosphere Drilling Project (ABDP-1) documented hematite as alteration products in 3.4 Ga basalts from the Marble Bar area of the Pilbara Craton, NW Australia, and this has been used to infer the presence of an O2-bearing atmosphere in the Archean. It is possible, however, that despite recovery of samples from > 100 m depth, oxidation of the basalts occurred much younger than the depositional age. In this study, the age of oxidation of the Apex Basalt from the ABDP-1 drill core at Marble Bar is constrained by U-Th-Pb geochronology. Lead and U concentrations of the basalts from the ABDP-1 drill core vary greatly, between < 1-58 ppm and 0.08-1.04 ppm, respectively, whereas Th contents are more restricted (0.24-0.71 ppm). 206Pb/204Pb ratios are non-radiogenic and vary from 12.44 to 14.69. The linear array in terms of 206Pb/204Pb-207Pb/204Pb variations does not reflect an age but reflects two-component mixing between a non-radiogenic "ore lead" end member and a radiogenic "basalt lead" end member. The samples do not form isochrons on 238U/204Pb-206Pb/204Pb, 235U/204Pb-207Pb/204Pb, or 232Th/204Pb-208Pb/204Pb diagrams, indicating post-formation U and Pb addition. Comparison of measured U/Th ratios with "model" U/Th ratios calculated based on 208Pb/204Pb-206Pb/204Pb variations indicates that U enrichment most likely occurred in the last 200 Ma. The degree of U enrichment in the samples is correlated with Fe(III)/FeTotal ratios, indicating that U addition and oxidation were related, most likely reflecting penetration of oxygenated surface waters in the Phanerozoic along bedding planes and shear zones. These results

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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

  12. 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

    USGS Publications Warehouse

    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.

  13. High-precision measurements of seawater Pb isotope compositions by double spike thermal ionization mass spectrometry.

    PubMed

    Paul, Maxence; Bridgestock, Luke; Rehkämper, Mark; van DeFlierdt, Tina; Weiss, Dominik

    2015-03-10

    A new method for the determination of seawater Pb isotope compositions and concentrations was developed, which combines and optimizes previously published protocols for the separation and isotopic analysis of this element. For isotopic analysis, the procedure involves initial separation of Pb from 1 to 2L of seawater by co-precipitation with Mg hydroxide and further purification by a two stage anion exchange procedure. The Pb isotope measurements are subsequently carried out by thermal ionization mass spectrometry using a (207)Pb-(204)Pb double spike for correction of instrumental mass fractionation. These methods are associated with a total procedural Pb blank of 28±21 pg (1sd) and typical Pb recoveries of 40-60%. The Pb concentrations are determined by isotope dilution (ID) on 50 mL of seawater, using a simplified version of above methods. Analyses of multiple aliquots of six seawater samples yield a reproducibility of about ±1 to ±10% (1sd) for Pb concentrations of between 7 and 50 pmol/kg, where precision was primarily limited by the uncertainty of the blank correction (12±4 pg; 1sd). For the Pb isotope analyses, typical reproducibilities (±2sd) of 700-1500 ppm and 1000-2000 ppm were achieved for (207)Pb/(206)Pb, (208)Pb/(206)Pb and (206)Pb/(204)Pb, (207)Pb/(204)Pb, (208)Pb/(204)Pb, respectively. These results are superior to literature data that were obtained using plasma source mass spectrometry and they are at least a factor of five more precise for ratios involving the minor (204)Pb isotope. Both Pb concentration and isotope data, furthermore, show good agreement with published results for two seawater intercomparison samples of the GEOTRACES program. Finally, the new methods were applied to a seawater depth profile from the eastern South Atlantic. Both Pb contents and isotope compositions display a smooth evolution with depth, and no obvious outliers. Compared to previous Pb isotope data for seawater, the (206)Pb/(204)Pb ratios are well correlated

  14. Plume-Lithosphere Interaction beneath the Snake River Plain, Idaho: Constraints from Pb, Sr, Nd, and Hf Isotopes

    NASA Astrophysics Data System (ADS)

    Jean, M. M.; Hanan, B. B.; Shervais, J. W.

    2011-12-01

    The Yellowstone-Snake River Plain (YSRP) volcanic province links 17 million years of volcanic activity that extends from the Owyhee Plateau in western Idaho/eastern Oregon to its current terminus underlying the Yellowstone Plateau. This investigation presents new Strontium, Neodymium, Lead, and Hafnium isotopic compositions of 25 basalts that represent four distinct areas of the YSRP (i.e., eastern province, central province, western province, Owyhee Plateau), which transect the ancient cratonic boundary of North America. The purpose of this study is to test and refine models for plume-lithosphere interaction and determines the mantle origin for YSRP basalts. New results shows: (1) low-K tholeiites from the eastern, central, and western SRP have ɛNd (-2 to -5.5), 87Sr/86Sr (0.7060-0.7071) and similar Pb-isotopes [206Pb/204Pb (17.8-18.6), 207Pb/204Pb (15.5-15.66), 208Pb/204Pb (38.4-39.1)]; (2) central SRP tholeiites are enriched in 208Pb/204Pb (~38.5-38.9), relative to eastern SRP basalts and define a 208Pb/204Pb trend, intermediate between the eastern SRP and Craters of the Moon lavas; (3) western SRP high-K basalts are depleted in ɛNd (> -1) and 87Sr/86Sr (0.7050-0.7057), relative to low-K tholeiites, and plot closer to "bulk silicate earth," but are enriched in 206Pb/204Pb (18.66-18.71), and have 207Pb/204Pb (15.62-15.65) and 208Pb/204Pb (39.1-39.2) isotope ratios similar to high-K basalts of Smith Prairie (Boise River Group 2); (4) Silver City basalt (>16.6 Ma) overlaps in Pb-isotope space with Imnaha basalt compositions (Columbia River Basalt Group); (5) new 177Hf/176Hf isotopic data lie above and parallel to the Mantle array in Nd and Hf isotope space and define a linear trend between Leucite Hills lavas and OIB basalts (i.e., Steens and Hawaii); (6) these basalts follow a systematic geographic pattern: eastern and central plain low-K tholeiites have low ɛNd (-3 to -5) and intermediate 206Pb/204Pb (~17.7-18.5), while western plain low-K tholeiites are

  15. Isotopic ratio based source apportionment of children's blood lead around coking plant area.

    PubMed

    Cao, Suzhen; Duan, Xiaoli; Zhao, Xiuge; Wang, Beibei; Ma, Jin; Fan, Delong; Sun, Chengye; He, Bin; Wei, Fusheng; Jiang, Guibin

    2014-12-01

    Lead exposure in the environment is a major hazard affecting human health, particularly for children. The blood lead levels in the local children living around the largest coking area in China were measured, and the source of blood lead and the main pathways of lead exposure were investigated based on lead isotopic ratios ((207)Pb/(206)Pb and (208)Pb/(206)Pb) in blood and in a variety of media, including food, airborne particulate matter, soil, dust and drinking water. The children's blood lead level was 5.25 (1.59 to 34.36 as range) μg dL(-1), lower than the threshold in the current criteria of China defined by the US Centers for Disease Control (10 μg dL(-1)). The isotopic ratios in the blood were 2.111±0.018 for (208)Pb/(206)Pb and 0.864±0.005 for (207)Pb/(206)Pb, similar to those of vegetables, wheat, drinking water, airborne particulate matter, but different from those of vehicle emission and soil/dust, suggesting that the formers were the main pathway of lead exposure among the children. The exposure pathway analysis based on the isotopic ratios and the human health risk assessment showed that dietary intake of food and drinking water contributed 93.67% of total exposed lead. The study further indicated that the coal used in the coking plant is the dominant pollution source of lead in children's blood.

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

    PubMed

    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. PMID:27376990

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

    PubMed

    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.

  18. Subducted upper and lower continental crust contributes to magmatism in the collision sector of the Sunda-Banda arc, Indonesia

    NASA Astrophysics Data System (ADS)

    Elburg, M. A.; van Bergen, M. J.; Foden, J. D.

    2004-01-01

    Pb isotopes in igneous rocks from the Banda-Sunda arc show extreme along-arc variations, which correspond to major lithologic changes in crustal components entering the subduction system. An increase in 206Pb/204Pb ratios toward the zone of collision with the Australian continent reflects input of subducted upper-crustal material; maximum values coincide with anomalously radiogenic 3He/4He ratios that have been earlier attributed to the involvement of the continental margin. The collision zone is further characterized by 208Pb/204Pb ratios that are higher for a given 207Pb/204Pb value than observed in the noncollisional sectors, and in the central part of the collision zone, the 206Pb/204Pb ratios are lower than the most radiogenic values in the adjacent areas. We propose that these Pb isotope signatures reflect input of subducted lower crust, mobilized as a result of slab-window formation during arc-continent collision. Variations in Pb isotopes in the collision zone are solely determined by variations in the nature and proportions of different subducted components. The Pb isotope arrays in the noncollision area may be dominated by slab components as well and could reflect mixing between subducted oceanic crust and entrained sediments, rather than between subarc mantle and subducted sediments. Our new interpretation of the Indonesian Pb isotope data does not call for involvement of ocean-island basalt (OIB) type mantle or Australian subcontinental lithospheric mantle, as has been suggested previously.

  19. Primitive and contaminated basalts from the Southern Rocky Mountains, U.S.A

    USGS Publications Warehouse

    Doe, B.R.; Lipman, P.W.; Hedge, C.E.; Kurasawa, H.

    1969-01-01

    Basalts in the Southern Rocky Mountains province have been analyzed to determine if any of them are primitive. Alkali plagioclase xenocrysts armored with calcic plagioclase seem to be the best petrographic indicator of contamination. The next best indicator of contamination is quartz xenocrysts armored with clinopyroxene. On the rocks and the region studied, K2O apparently is the only major element with promise of separating primitive basalt from contaminated basalt inasmuch as it constitutes more than 1 % in all the obviously contaminated basalts. K2O: lead (> 4 ppm) and thorium (> 2 ppm) contents and Rb/Sr (> 0.035) are the most indicative of the trace elements studied. Using these criteria, three basalt samples are primitive (although one contains 1.7% K2O) and are similar in traceelement contents to Hawaiian and Eastern Honshu, Japan, primitive basalts. Contamination causes lead isotope ratios, 206Pb/204Pb and 208Pb/204Pb, to become less radiogenic, but it has little or no effect on 87Sr/86Sr. We interpret the effect on lead isotopes to be due to assimilation either of lower crustal granitic rocks, which contain 5-10 times as much lead as basalt and which have been low in U/Pb and Th/Pb since Precambrian times, or of upper crustal Precambrian or Paleozoic rocks, which have lost much of their radiogenic lead because of heating prior to assimilation. The lack of definite effects on strontium isotopes may be due to the lesser strontium contents of granitic crustal rocks relative to basaltic rocks coupled with lack of a large radiogenic enrichment in the crustal rocks. Lead isotope ratios were found to be less radiogenic in plagioclase separates from an obviously contaminated basalt than in the primitive basalts. The feldspar separate that is rich in sodic plagioclase xenocrysts was found to be similar to the whole-rock composition for 206Pb/204Pb and 208Pb/204Pb whereas a more dense fraction probably enriched in more calcic plagioclase phenocrysts is more similar

  20. Improved 206Pb/238U microprobe geochronology by the monitoring of a trace-element-related matrix effect; SHRIMP, ID-TIMS, ELA-ICP-MS and oxygen isotope documentation for a series of zircon standards

    USGS Publications Warehouse

    Black, L.P.; Kamo, S.L.; Allen, C.M.; Davis, D.W.; Aleinikoff, J.N.; Valley, J.W.; Mundil, R.; Campbell, I.H.; Korsch, R.J.; Williams, I.S.; Foudoulis, C.

    2004-01-01

    Precise isotope dilution-thermal ionisation mass spectrometry (ID-TIMS) documentation is given for two new Palaeozoic zircon standards (TEMORA 2 and R33). These data, in combination with results for previously documented standards (AS3, SL13, QGNG and TEMORA 1), provide the basis for a detailed investigation of inconsistencies in 206Pb/238U ages measured by microprobe. Although these ages are normally consistent between any two standards, their relative age offsets are often different from those established by ID-TIMS. This is true for both sensitive high-resolution ion-microprobe (SHRIMP) and excimer laser ablation-inductively coupled plasma-mass spectrometry (ELA-ICP-MS) dating, although the age offsets are in the opposite sense for the two techniques. Various factors have been investigated for possible correlations with age bias, in an attempt to resolve why the accuracy of the method is worse than the indicated precision. Crystallographic orientation, position on the grain-mount and oxygen isotopic composition are unrelated to the bias. There are, however, striking correlations between the 206Pb/238U age offsets and P, Sm and, most particularly, Nd abundances in the zircons. Although these are not believed to be the primary cause of this apparent matrix effect, they indicate that ionisation of 206Pb/238U is influenced, at least in part, by a combination of trace elements. Nd is sufficiently representative of the controlling trace elements that it provides a quantitative means of correcting for the microprobe age bias. This approach has the potential to reduce age biases associated with different techniques, different instrumentation and different standards within and between laboratories. Crown Copyright ?? 2004 Published by Elsevier B.V. All rights reserved.

  1. Levels and source apportionment of children's lead exposure: could urinary lead be used to identify the levels and sources of children's lead pollution?

    PubMed

    Cao, Suzhen; Duan, Xiaoli; Zhao, Xiuge; Wang, Beibei; Ma, Jin; Fan, Delong; Sun, Chengye; He, Bin; Wei, Fusheng; Jiang, Guibin

    2015-04-01

    As a highly toxic heavy metal, the pollution and exposure risks of lead are of widespread concern for human health. However, the collection of blood samples for use as an indicator of lead pollution is not always feasible in most cohort or longitudinal studies, especially those involving children health. To evaluate the potential use of urinary lead as an indicator of exposure levels and source apportionment, accompanying with environmental media samples, lead concentrations and isotopic measurements (expressed as (207)Pb/(206)Pb, (208)Pb/(206)Pb and (204)Pb/(206)Pb) were investigated and compared between blood and urine from children living in the vicinities of a typical coking plant and lead-acid battery factory. The results showed urinary lead might not be a preferable proxy for estimating blood lead levels. Fortunately, urinary lead isotopic measurements could be used as an alternative for identifying the sources of children's lead exposure, which coincided well with the blood lead isotope ratio analysis.

  2. Levels and source apportionment of children's lead exposure: could urinary lead be used to identify the levels and sources of children's lead pollution?

    PubMed

    Cao, Suzhen; Duan, Xiaoli; Zhao, Xiuge; Wang, Beibei; Ma, Jin; Fan, Delong; Sun, Chengye; He, Bin; Wei, Fusheng; Jiang, Guibin

    2015-04-01

    As a highly toxic heavy metal, the pollution and exposure risks of lead are of widespread concern for human health. However, the collection of blood samples for use as an indicator of lead pollution is not always feasible in most cohort or longitudinal studies, especially those involving children health. To evaluate the potential use of urinary lead as an indicator of exposure levels and source apportionment, accompanying with environmental media samples, lead concentrations and isotopic measurements (expressed as (207)Pb/(206)Pb, (208)Pb/(206)Pb and (204)Pb/(206)Pb) were investigated and compared between blood and urine from children living in the vicinities of a typical coking plant and lead-acid battery factory. The results showed urinary lead might not be a preferable proxy for estimating blood lead levels. Fortunately, urinary lead isotopic measurements could be used as an alternative for identifying the sources of children's lead exposure, which coincided well with the blood lead isotope ratio analysis. PMID:25617855

  3. Petrogenesis of pegmatites and granites in southwestern Maine

    SciTech Connect

    Tomascak, P.B.; Walker, R.J.; Krogstad, E.J. . Dept. of Geology)

    1993-03-01

    Granitic pegmatites occurring near the town of Topsham in southwestern Maine are mineralogically diverse, featuring abundant dikes and contain rare earth element minerals as well as one pegmatite that contains Li minerals. The pegmatite series crops out near the Brunswick granite, a texturally diverse granitic pluton, and lies 13 km southeast of the Mississippian age Sebago batholith. Areas intruded by pegmatites that possess such different mineral assemblages are globally rare. The origins of these mixed'' pegmatite series have not been comprehensively investigated. There is no known pattern of regional zonation (mineral/chemical) among Topsham series pegmatites, hence simple fractionation processes are probably not responsible for the compositional variations. The authors are attempting to clarify pegmatite petrogenesis using common Pb isotopic ratios of feldspars and Sm-Nd isotopic data from whole rocks and minerals. Pb isotopic ratios from leached feldspars reflect the Pb ratios of the source from which they were derived. The range of Pb isotopic compositions of alkali feldspars from 7 granitic pegmatites is as follows: [sup 206]Pb/[sup 204]Pb = 18.5-19.1; [sup 207]Pb/[sup 204]Pb = 15.53-15.69; [sup 208]Pb/[sup 204]Pb = 38.3-38.6. The Brunswick granite has K-feldspars with [sup 206]Pb/[sup 204]Pb = 18.40-18.47, [sup 207]/[sup 204]Pb = 15.64-15.66 and [sup 208]Pb/[sup 204]Pb = 38.29-38.39. The Pb isotopic compositions of both pegmatites and granites are significantly more radiogenic than existing data for the Sebago granite and argue against the consanguinity of Topsham pegmatites and the Sebago batholith. These data instead support a genetic link between the pegmatites and the Brunswick granite, which ranges from a fine-grained two-mica granite to a garnet-bearing pegmatitic leucogranite.

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

    PubMed

    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 (p<0.05) increases in blood-lead 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.

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

    PubMed

    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

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

    NASA Astrophysics Data System (ADS)

    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

  7. Sr-Pb isotopic studies of primitive and near-primitive basaltic magmas, Garibaldi volcanic belt, northern Cascadia subduction system

    NASA Astrophysics Data System (ADS)

    Green, N. L.; Sinha, A. K.

    2003-12-01

    The northern Cascadia subduction system is intimately associated with aseismic subduction of extremely young and presumably `hot' oceanic lithosphere beneath northwestern Washington and southwestern British Columbia. Sr and Pb isotopic analyses are presented for primitive and near-primitive (>6.0 wt. % MgO) basalts from a southeast-northwest transect along the Garibaldi volcanic belt (GVB), which overlies subducted oceanic lithosphere that decreases in age from ca. 22 m.y. below Glacier Peak at its southern end to about 13 m.y. beneath the northernmost eruptive centers in the Mosaic (Meager Mountain) and Salal Glacier-Bridge River areas. The basaltic rocks have initial 87Sr/86Sr ratios of 0.70317-0.70426, with minimum observed values in individual lava suites decreasing northward. Values of Pb isotopic ratios for GVB basaltic suites range from 18.22 to 18.97 for 206Pb/204Pb, from 15.51 to 15.59 for 207Pb/204Pb, and from 37.73 to 38.49 for 208Pb/204Pb. Sr isotopic compositions, unsupported by lava Rb contents, show positive correlations with Cs/Rb, La/Nb, Ba/La, Ba/Nb, Ba/Ta, B/La, B/Zr, Sr/Nd, and primitive mantle normalized Sr/P; and negative correlations with high field strength elements (HFSE: Nb, and Ta), FeO and other transition metals (Co and Zn), Ce/Pb,Cr/Ni, Sm/Yb, Ta/Yb, Hf/Yb, K/Ba, K/Sr, and La/Yb. Moderate to strong correlations between 87Sr/86Sr and ratios involving fluid-mobile and less-fluid-mobile elements are compatible with decreased slab input northward along the volcanic front as the subducted plate becomes hotter. The Pb isotopic compositions exhibit only limited variations when examined against position along the volcanic arc, but show uniform to extremely weak positive correlations of 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb with 87Sr/86Sr, Ba/La, Sr/Nd, Ba/Nb, Zr/Nb, Mg-Number and SiO2; and similarly weak negative correlation of Ce/Pb with 206Pb/204Pb and 207Pb/204Pb. The isotopic data suggest that GVB basaltic magmas have experienced with

  8. Quaternary geochronology using the U-Th-Pb method

    SciTech Connect

    Getty, S.R.; DePaolo, D.J.

    1995-08-01

    We describe a method of uranium-thorium-lead (U-Th-Pb) isotopic age dating for Quaternary rocks. The approach uses an instrumental mass discrimination correction for lead isotope ratios, which allows small enrichments of radiogenic {sup 206}Pb and {sup 208}Pb to be detected at the level of 0.001%. Igneous rocks hosting minerals with a range in {sup 238}U/{sup 204}Pb values of 100 can be dated with uncertainties of approximately {+-}15-20 kyr. A Quarternary rhyolite dated at 1.19 Ma by K-Ar yields a {sup 238}U-{sup 206}Pb age of 1.03{+-}0.10 Ma. A Holocene dacite (9.5 ka) has uniform {sup 206}Pb/{sup 207}Pb to within {+-}0.0015% in groundmass phases, but 1 mm plagioclase phenocrysts have lower {sup 206}Pb/{sup 207}Pb by 0.105{+-}0.002% indicating contamination of the magma after plagioclase crystallization. High precision {sup 206}Pb/{sup 207}Pb ratios may be a useful new tool for petrogenetic studies.

  9. Characteristics and genesis of mineral deposits in East Ujimqin Banner, western segment of the Great Xing'an Mountains, NE China

    NASA Astrophysics Data System (ADS)

    Zhang, Wanyi; Nie, Fengjun; Liu, Shuwen; Zuo, Liyan; Yao, Xiaofeng; Jia, Delong; Liu, Jiangtao

    2015-01-01

    The East Ujimqin Banner, located in the western segment of the Great Xing'an Mountains, NE China, has undergone a long and multi-stage tectonic evolution, which has resulted in significant Fe-Ag-Pb-Zn-Au-Cu-Mo deposits. There are two main types of mineralization: vein and skarn types. The Jilinbaolige and Aerhada vein deposits, and the Chagan Obo and Chaobuleng skarn-type deposits are four typical deposits in this area. The vein deposits mainly occur as veins with hydrothermal alteration in fractures within pre-mineralization clastic rocks and felsic volcanic rocks. The skarn-type deposits always show a temporal and spatial relationship with Mesozoic granite intruded into Paleozoic limestone. The sulfur isotope data from the sulfides in these four deposits have a very narrow range (+1‰ to +8‰), suggesting that most were derived from magma. The 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios range from 17.949 to 18.529, 15.370 to 15.691 and 37.653 to 38.460 respectively, indicating that the metals derive mainly from the mantle source. In the diagrams 207Pb/204Pb vs. 206Pb/204Pb and 208Pb/204Pb vs. 206Pb/204Pb, the points of lead isotope of the sulfide ores are very near or coincide to the K-feldspar, indicating that the ore-forming materials sources have the genetic relationship. It seems that there are four key factors controlling the mineralization styles in this district: the tectonic setting, magmatic activity, wall rocks, and structures. The superposition of multi-stage tectonism from a Mesozoic extensional setting on a Paleozoic subduction setting provided a remobilization and enrichment mechanism for the ore-forming elements. The magmatic activities were sources of metals and fluids, and drove them to the mineralization sites. The wall rocks are key factors for mineralization styles. When metal-bearing fluid flows into clastic rocks and felsic volcanic rocks, the mineralization is mainly vein type, and mineralization in limestone is mainly skarn type. NE

  10. Temporal variation of isotope and rare earth element abundances in volcanic rocks from Guam: implications for the evolution of the Mariana Arc

    NASA Astrophysics Data System (ADS)

    Hickey-Vargas, Rosemary; Reagan, Mark K.

    1987-12-01

    Volcanic rocks exposed on Guam were erupted during the Late Middle Eocene (Facpi Fm.), Late Eocene-Oligocene (Alutom Fm.) and Miocene (Umatac Fm.). Four magma series are recognized: the boninite series (44 m.y.b.p.), the tholeiite and calc-alkaline series, which were erupted along with boninite series lavas at 32 36 m.y.b.p. and high-K lavas of the Umatac Fm. (14 m.y.b.p.). Isotope and and rare earth element (REE) characteristics of the four magma series are distinct. Boninite series lavas have U-shaped REE patterns, relatively low 143Nd/144Nd (0.51294 0.51298), and high 206Pb/204Pb (19.0 19.2). Tholeiite series lavas are LREE (light REE) depleted, and have high 143Nd/144Nd (0.51304 0.51306) and low 206Pb/204Pb (18.4 18.5). Calc-alkaline series lavas have Sr, Nd and Pb isotope ratios similar to tholeiite series lavas, but flat to U-shaped REE patterns. Umatac Fm. lavas are strongly LREE-enriched, and have higher 87Sr/ 86Sr (0.70375 0.70380) and 207Pb/204Pb relative to 206Pb/ 204Pb than Facpi and Alutom Fm. lavas. Boninite and tholeiite series magmas, erupted in the position of the Palau-Kyushu Ridge, were probably derived from distinct mantle sources having OIB and N-MORB-like isotopic characteristics, together with fluids derived from subducted Pacific plate basalt. Calc-alkaline series lavas were most likely derived from the tholeiite series by extensive crystal fractionation, wallrock contamination and magma mixing. Lavas of the Umatac Fm., erupted in the position of the West Mariana Ridge, may include up to 2 3% subducted sediment, similar to some active Mariana arc lavas.

  11. Strong Relationship between Hf-Nd-Pb Isotopes in Atlantic Sediments and the Lesser Antilles arc Composition

    NASA Astrophysics Data System (ADS)

    Carpentier, M.; Chauvel, C.; Mattielli, N.

    2006-12-01

    Geochemical variability of lavas from the Lesser Antilles arc is well established and is characterized by a chemical zoning from north to south along the arc. Lavas from the northern part of the arc have usually less radiogenic and less variable Sr and Pb isotopic compositions than those from the south. Possible explanations include a larger contribution from sediments in the source of the southern islands, and/or a north-south change in the chemical composition of the sediments that are subducted beneath the Lesser Antilles arc We conducted a geochemical study (Nd, Hf and Pb isotopic compositions) of Atlantic sediments coming from two different sites drilled during DSDP Leg 78 (site 543, 15.7N) and DSDP Leg 14 (site 144, 9.5N). At site 543, the sedimentary pile has epsilon Nd values between -14.6 and -11 and epsilon Hf between -10.6 and -1. 206Pb/204Pb ratios vary between 19.1 and 19.5. The sediment pile has an overall strong continental signature suggesting that their source is primarily detrital. This is in agreement with the interpretation of White et al. (1985) who suggested that the dominant source was the Archean Guiana Highland drained by the Orinoco River. Further south, at site 144, the succession consists of chalk ooze, marl and clays, and organic-rich black shales. Samples have epsilon Nd between -18.4 and -10 and epsilon Hf between -20.4 and -5.4 and the Pb isotopic compositions are extremely variable. Chalk ooze, marl and clay have 206Pb/204Pb ratios between 18.8 and 20.0, while the black shales have extremely radiogenic compositions with 206Pb/204Pb between 21.6 and 27.7. These compositions reflect the radioactive decay of authigenic uranium concentrated in organic- rich layers characterized by elevated 238U/204Pb ratios (100 up to 600). The isotopic compositions of sediments from both sites are largely influenced by continental input with Nd and Hf isotopes plotting in the continental domain of the "terrestrial array", but the southern site has more

  12. The geochemical and Sr-Nd-Pb-He isotopic characterization of the mantle source of Rungwe Volcanic Province: comparison with the Afar mantle domain

    NASA Astrophysics Data System (ADS)

    Castillo, P. R.; Hilton, D. R.; Halldorsson, S. A.; Wang, R.

    2012-12-01

    The ultimate source of heat and magmatism associated with continental rifting in the East African Rift System (EARS) is generally viewed to be the African Superplume, but there is continuing debate on the surface expression of this large anomalous feature, which originates in the lower mantle. Previous studies have demonstrated an insignificant role for crustal contamination thereby identifying a single mantle plume signature in Quaternary basalts from the Main Ethiopian Rift in the northern EARS. This is designated to be the Afar plume and is characterized by, e.g., 3He/4He >15 RA, 206Pb/204Pb = 19.5 and 87Sr/86Sr = 0.7035 [Rooney et al., J. Pet. 53, 2012]. In contrast, the signature of plume(s) in the southern EARS is less constrained. Rogers et al. [EPSL 176, 2000] proposed a plume in the sub-lithospheric Kenyan mantle with characteristically lower 43Nd/144Nd than the Afar plume whereas Furman [JAES 48, 2007] advocated a high μ [HIMU] plume based primarily on the high 206Pb/204Pb ratios of lavas in all areas within and south of the Turkana Depression: both models assume a 3He/4He lower than the Afar plume. Here we report the trace element and Sr-Nd-Pb isotopic composition of basaltic lavas from the Rungwe Volcanic Province (RVP) in the southern extreme of the Western Rift previously identified as a high 3He/4He locality (~15 RA; [Hilton et al., GRL 38, 2011]). Trace element analyses are within the previously reported range of lava compositions that include a relatively large lithospheric component. More importantly, we identify correlations among incompatible trace element and isotopic ratios (e.g., 3He/4He vs 206Pb/204Pb, Rb/Sr, Nb/Ta; 87Sr/86Sr vs 208Pb/204Pb). Our new results suggest the presence of a distinct, high 3He/4He mantle source beneath RVP that is more radiogenic (e.g., 206Pb/204Pb up to ~19.8; 87Sr/86Sr up to 0.7055) than the Afar mantle plume. There is also very little or no HIMU signature in RPV basalts based on their high Sr and low Nd isotopic

  13. Pbsbnd Srsbnd Nd isotopic tracing of the influence of the Amazon River on the bottom sediments in the lower Tapajós River

    NASA Astrophysics Data System (ADS)

    Medeiros Filho, Lucio C.; Lafon, Jean-Michel; Souza Filho, Pedro Walfir M.

    2016-10-01

    The isotopic signatures of Pbsbnd Srsbnd Nd in recent bottom sediments were used to investigate the hydrodynamics of the lower stream of the Tapajós River and its interaction with the Amazon River. Samples from the Tapajós River have Pb isotopic ratios (19.67 < 206Pb/204Pb < 20.02; 15.87 < 207Pb/204Pb < 15.91) different from those of the bottom sediments found downstream in the Amazon River (18.84 < 206Pb/204Pb < 18.94; 207Pb/204Pb ≈ 15.67). In the confluence zone, the ratios have intermediate values (18.69 < 206Pb/204Pb < 19.53; 15.65 < 207Pb/204Pb < 15.83). The sediments in the Tapajós River have lower ɛNd(0) (-21 < ɛNd(0) < -19) values and more radiogenic isotopic Sr ratios (87Sr/86Sr ≈ 0.792) than those of the sediments from the Amazon River (ɛNd(0) ≈ -9 and 0.712 < 87Sr/86Sr < 0.716). The isotopic data suggest that the Amazon River influences the sediments in the Tapajós River, but this influence is restricted to the confluence zone. Additionally, the concentrations of major and trace elements and the mineralogy of the sediments are in agreement with the isotopic data. We conclude that the accumulation of muddy sediments in the lower stream of the Tapajós River is a result of the influence of the Amazon River, which retains this discharge from its affluent thus generating favorable conditions for depositing the finer sediments coming from the Tapajós River without any significant contribution of sediments from the Amazon River itself. The values of ɛNd(0) and TDM and of 87Sr/86Sr ratio of the Tapajós River bottom sediments indicate that the source of the sediments is essentially the erosion of the Paleoproterozoic felsic units from the Tapajós (2.03-1.88 Ga) and Juruena (1.82-1.54 Ga) geotectonic provinces.

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

    PubMed

    Wang, Wan; Liu, Xiande; Zhao, Liwei; Guo, Dongfa; Tian, Xiaodan; Adams, Freddy

    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 206Pb/207Pb ratio was lower in summer, when coal combustion emission was low and vehicle exhaust became more important, indicating that the 206Pb/207Pb ratio of leaded petrol in Tianjin is lower than that of aerosol samples. The 206Pb/207Pb 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.

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

    PubMed

    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 < 0.01), and 206Pb:207Pb ratios for worms and soils were also positively correlated (r = 0.54; p < 0.05). However, most young-of-the-year woodcock with high bone-Pb accumulation (> 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. PMID:14587896

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

    PubMed

    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 < 0.01), and 206Pb:207Pb ratios for worms and soils were also positively correlated (r = 0.54; p < 0.05). However, most young-of-the-year woodcock with high bone-Pb accumulation (> 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. Changes in the lead isotopic composition of blood, diet and air in Australia over a decade: Globalization and implications for future isotopic studies

    SciTech Connect

    Gulson, Brian . E-mail: bgulson@gse.mq.edu.au; Mizon, Karen; Korsch, Michael; Taylor, Alan

    2006-01-15

    Source apportionment in biological or environmental samples using the lead isotope method, where there are diverse sources of lead, relies on a significant difference between the isotopic composition in the target media and the sources. Because of the unique isotopic composition of Australian lead, source apportionment has been relatively successful in the past. Over the period of a decade, the {sup 206}Pb/{sup 204}Pb ratio for Australian (mainly female) adults has shown an increase from a geometric mean of 16.8-17.3. Associated with this increase, there has been a decrease in mean blood lead concentration from 4.7 to 2.3 {mu}g/dL, or about 5% per year, similar to that observed in other countries. Lead in air, which up until 2000 was derived largely from the continued use of leaded gasoline, showed an overall increase in the {sup 206}Pb/{sup 204}Pb ratio during 1993-2000 from 16.5 to 17.2. Since 1998 the levels of lead in air were less than 0.2 {mu}g/m{sup 3} and would contribute negligibly to blood lead. Over the 10-year period, the {sup 206}Pb/{sup 204}Pb ratio in diet, based mainly on quarterly 6-day duplicate diets, increased from 16.9 to 18.3. The lead concentration in diet showed a small decrease from 8.7 to 6.4 {mu}g Pb/kg although the daily intake increased markedly from 7.4 to 13.9 {mu}g Pb/day during the latter part of the decade probably reflecting differences in demographics. The changes in blood lead from sources such as lead in bone or soil or dust is not dominant because of the low {sup 206}Pb/{sup 204}Pb ratios in these media. Unless there are other sources not identified and analysed for these adults, it would appear that in spite of our earlier conclusions to the contrary, diet does make an overall contribution to blood lead, and this is certainly the case for specific individuals. Certain population groups from south Asia, south-east Asia, the Middle East and Europe (e.g. UK) are unsuitable for some studies as their isotopic ratios in blood are

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

    NASA Astrophysics Data System (ADS)

    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. Uranium-lead isotope systematics of Mars inferred from the basaltic shergottite QUE 94201

    SciTech Connect

    Gaffney, A M; Borg, L E; Connelly, J N

    2006-12-22

    Uranium-lead ratios (commonly represented as {sup 238}U/{sup 204}Pb = {mu}) calculated for the sources of martian basalts preserve a record of petrogenetic processes that operated during early planetary differentiation and formation of martian geochemical reservoirs. To better define the range of {mu} values represented by the source regions of martian basalts, we completed U-Pb elemental and isotopic analyses on whole rock, mineral and leachate fractions from the martian meteorite Queen Alexandra Range 94201 (QUE 94201). The whole rock and silicate mineral fractions have unradiogenic Pb isotopic compositions that define a narrow range ({sup 206}Pb/{sup 204}Pb = 11.16-11.61). In contrast, the Pb isotopic compositions of weak HCl leachates are more variable and radiogenic. The intersection of the QUE 94201 data array with terrestrial Pb in {sup 206}Pb/{sup 204}Pb-{sup 207}Pb/{sup 204}Pb-{sup 208}Pb/{sup 204}Pb compositional space is consistent with varying amounts of terrestrial contamination in these fractions. We calculate that only 1-7% contamination is present in the purified silicate mineral and whole rock fractions, whereas the HCl leachates contain up to 86% terrestrial contamination. Despite the contamination, we are able to use the U-Pb data to determine the initial {sup 206}Pb/{sup 204}Pb of QUE 94201 (11.086 {+-} 0.008) and calculate the {mu} value of the QUE 94201 mantle source to be 1.823 {+-} 0.008. This is the lowest {mu} value calculated for any martian basalt source, and, when compared to the highest values determined for martian basalt sources, indicates that {mu} values in martian source reservoirs vary by at least 100%. The range of source {mu} values further indicates that the {mu} value of bulk silicate Mars is approximately three. The amount of variation in the {mu} values of the mantle sources ({mu} {approx} 2-4) is greater than can be explained by igneous processes involving silicate phases alone. We suggest the possibility that a small

  20. Pb-concentrations and Pb-isotope ratios in soils collected along an east-west transect across the United States

    USGS Publications Warehouse

    Reimann, Clemens; Smith, David B.; Woodruff, Laurel G.; Flem, Belinda

    2011-01-01

    Analytical results for Pb-concentrations and isotopic ratios from ca. 150 samples of soil A horizon and ca. 145 samples of soil C horizon collected along a 4000-km east–west transect across the USA are presented. Lead concentrations along the transect show: (1) generally higher values in the soil A-horizon than the C-horizon (median 21 vs. 16.5 mg/kg), (2) an increase in the median value of the soil A-horizon for central to eastern USA (Missouri to Maryland) when compared to the western USA (California to Kansas) (median 26 vs. 20 mg/kg) and (3) a higher A/C ratio for the central to eastern USA (1.35 vs. 1.14). Lead isotopes show a distinct trend across the USA, with the highest 206Pb/207Pb ratios occurring in the centre (Missouri, median A-horizon: 1.245; C-horizon: 1.251) and the lowest at both coasts (e.g., California, median A-horizon: 1.195; C-horizon: 1.216). The soil C-horizon samples show generally higher 206Pb/207Pb ratios than the A-horizon (median C-horizon: 1.224; A-horizon: 1.219). The 206Pb/207Pb-isotope ratios in the soil A horizon show a correlation with the total feldspar content for the same 2500-km portion of the transect from east-central Colorado to the Atlantic coast that shows steadily increasing precipitation. No such correlation exists in the soil C horizon. The data demonstrate the importance of climate and weathering on both Pb-concentration and 206Pb/207Pb-isotope ratios in soil samples and natural shifts thereof in the soil profile during soil-forming processes.

  1. The petrogenesis of volcanics from Mt. Bulusan and Mt. Mayon in the Bicol arc, the Philippines

    NASA Astrophysics Data System (ADS)

    McDermott, Frank; , Francisco G. Delfin, Jr.; Defant, Marc J.; Turner, Simon; Maury, Rene

    2005-12-01

    Pliocene to recent volcanic rocks from the Bulusan volcanic complex in the southern part of the Bicol arc (Philippines) exhibit a wide compositional range (medium- to high-K basaltic-andesites, andesites and a dacite/rhyolite suite), but are characterised by large ion lithophile element enrichments and HFS element depletions typical of subduction-related rocks. Field, petrographic and geochemical data indicate that the more silicic syn- and post-caldera magmas have been influenced by intracrustal processes such as magma mixing and fractional crystallisation. However, the available data indicate that the Bicol rocks as a group exhibit relatively lower and less variable 87Sr/86Sr ratios (0.7036-0.7039) compared with many of the other subduction-related volcanics from the Philippine archipelago. The Pb isotope ratios of the Bicol volcanics appear to be unlike those of other Philippine arc segments. They typically plot within and below the data field for the Philippine Sea Basin on 207Pb/204Pb versus 206Pb/204Pb and 208Pb/204Pb versus 206Pb/204Pb diagrams, implying a pre-subduction mantle wedge similar to that sampled by the Palau Kyushu Ridge, east of the Philippine Trench. 143Nd/144Nd ratios are moderately variable (0.51285-0.51300). Low silica (<55 wt%) samples that have lower 143Nd/144Nd tend to have high Th/Nd, high Th/Nb, and moderately low Ce/Ce* ratios. Unlike some other arc segments in the Philippines (e.g. the Babuyan-Taiwan segment), there is little evidence for the involvement of subducted terrigenous sediment. Instead, the moderately low 143Nd/144Nd ratios in some of the Bicol volcanics may result from subduction of pelagic sediment (low Ce/Ce*, high Th/Nd, and high Th/Nb) and its incorporation into the mantle wedge via a slab-derived partial melt.

  2. Character of the pre-Mesozoic basement along the edge of the western US craton: Pb isotopic evidence from Mesozoic plutonism

    SciTech Connect

    Wooden, J.L.; Kistler, R.W.; Robinson, A.; Tosdal, R.M. ); Wright, J.E. . Dept. of Geology and Geophysics)

    1993-04-01

    The pre-Mesozoic cratonic crust of the western US was a composite of provinces composed mostly of Archean and Early Proterozoic rocks that had been truncated by Late Proterozoic rifting and had some new Paleozoic crust added along the western edge. Mesozoic and younger geologic events greatly obscured this pre-Mesozoic basement along the craton edge. However, the Pb isotopic signatures of Mesozoic plutons provide significant clues to the character of the crust in which they formed or were emplaced because of a strong contrast in Pb concentration between low-Pb, mantle-derived melts and Pb-rich crust. Thus, magmas whether derived from the crust or the mantle with subsequent crustal interaction, will likely have Pb isotopic compositions that reflect those of the crust. In the western US the Pb isotopic compositions of Mesozoic plutonic rocks have strong regional characteristics. Within the Early Proterozoic Mojave crustal province, Mesozoic plutonic rocks have a large range of 206Pb/204Pb ratios that plot above the crustal average, relatively high 207Pb/204Pb ratios that suggest an Archean contribution, and Pb and Sr isotopic compositions that are not correlated and that do not distinguish age groups. At the southern and western edge of this province where some 1.1 Ga rocks are exposed, 208Pb/204Pb ratios lie along the average crust model curve. These data suggest that any individual pluton provides a composite Pb isotopic composition for a discrete vertical section of the crust. Pb isotopic compositions of plutons in the Sierra Nevada and Great Basin are very different from those described above with 206Pb/204Pb ratios starting at 18.6, well-correlated Pb isotopic trends starting below the crustal model but extending to values that require input from the very radiogenic Wyoming province Archean crust, and good correlations between Pb and (1) Sr isotopic compositions and (2) W-E geographic position.

  3. The Rurutu Hotspot: Isotopic and Trace Element Evidence of HIMU Hotspot Volcanism in the Tuvalu Islands

    NASA Astrophysics Data System (ADS)

    Finlayson, V.; Konter, J. G.; Konrad, K.; Koppers, A. A. P.; Jackson, M. G.

    2014-12-01

    Current Pacific absolute plate motion (APM) models include 2 major, long-lived hotspot tracks: the ~85 Ma Hawaiian-Emperor and the ~76 Ma Louisville tracks. Prior to ~50 Ma, these two hotspot tracks show significant inter-hotspot drift, mainly due to large southern motion of the Hawaiian hotspot [1,2]. A third track would allow for a more robust evaluation of the relationship between APM models and inter-hotspot drift. We present trace element and Pb isotope evidence for a potential third long-lived Pacific hotspot trail—the Rurutu hotspot—anchored in the Cook-Austral Islands. Based on high 206Pb/204Pb ratios, 70-55 Ma volcanism in the Gilbert Ridge has been linked to the Rurutu hotspot [3]. The Gilbert Ridge may continue south into the Tuvalu Islands, where APM models predict that the Rurutu hotspot track captures the change in Pacific plate motion around 50 Ma at the intersection of Tuvalu and Samoa. Sampling of the deep submarine flanks of atolls and seamounts in Tuvalu and westernmost Samoa took place during the 2013 RR1310 (R/V Roger Revelle) expedition. We present new Pb isotope and HFSE trace element data on 28 samples that support a Rurutu origin for Tuvalu volcanism and confirm HIMU signatures previously observed in 5 Tuvalu samples (206Pb/204Pb >20.1, several >21.0; 87Sr/86Sr < 0.705). Statistical tests indicate that Tuvalu HFSE element ratios show similarities with Cook-Austral HIMU and differences with Samoa EMII volcanism. Low Hf/Nb ratios are often a predictor of HIMU samples (206Pb/204Pb > 20.8). Moderately HIMU compositions (206Pb/204Pb = 20.0) correspond to slightly higher Hf/Nb. In an effort to test if compositional agreement with the Cook-Australs is reflected in an age progression, 40Ar/39Ar ages will be presented by Konrad et al. (this volume). [1] Tarduno et al., (2003) DOI:10.1126/science.1086442 [2] Koppers et al., (2012) DOI: 10.1038/ngeo1638 [3] Konter et al., (2008) DOI: 10.1016/j.epsl.2008.08.023

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

    PubMed

    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.

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

    PubMed

    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. PMID:23871578

  6. The recycling of marine carbonates and sources of HIMU and FOZO ocean island basalts

    NASA Astrophysics Data System (ADS)

    Castillo, Paterno R.

    2015-02-01

    Many, and perhaps all, oceanic island basalts (OIB) clearly contain a component of crustal materials that have been returned to the mantle through subduction or other processes. One of the first recycled materials to be identified as a potential source of OIB was mid-ocean ridge basalt (MORB), and this was later fine-tuned as having a long time-integrated (b.y.) high U/Pb ratio or high μ (HIMU) and producing OIB with the most radiogenic Pb isotopic ratios (206Pb/204Pb > 20). However, it is becoming more evident that the compositional connection between subducted MORB and HIMU basalts is problematic. As an alternative hypothesis, a small amount (a few %) of recycled Archaean marine carbonates (primarily CaCO3) is proposed to be the main source of the distinct 206Pb/204Pb, 207Pb/204Pb and 87Sr/86Sr isotopic and major-trace element compositions of classic HIMU and post-Archaean marine carbonates for younger HIMU or the so-called FOZO mantle source. As an extension of the hypothesis, a conceptual model that combines the separate evolutionary histories of ancient oceanic lithosphere, which is the source of OIB, and upper mantle, which is the source of MORB, is also proposed. The model claims that FOZO mainly consists of the lithospheric mantle portion of the ancient metamorphosed oceanic slabs that have accumulated in the deep mantle. Such an ultramafic source is geochemically depleted due to prior extraction of basaltic melt plus removal of the enriched subduction component from the slab through dehydration and metamorphic processes. Combined with other proposed models in the literature, the conceptual model can provide reasonable solutions for the 208Pb/204Pb, 143Nd/144Nd, 176Hf/177Hf, and 3He/4He isotopic paradoxes or complexities of oceanic lavas. Although these simultaneous solutions for individual paradoxes are qualitative and non-unique, these are unified under a single, marine carbonate recycling hypothesis.

  7. Ratio

    NASA Astrophysics Data System (ADS)

    Webster, Nathan A. S.; Pownceby, Mark I.; Madsen, Ian C.; Studer, Andrew J.; Manuel, James R.; Kimpton, Justin A.

    2014-12-01

    Effects of basicity, B (CaO:SiO2 ratio) on the thermal range, concentration, and formation mechanisms of silico-ferrite of calcium and aluminum (SFCA) and SFCA-I iron ore sinter bonding phases have been investigated using an in situ synchrotron X-ray diffraction-based methodology with subsequent Rietveld refinement-based quantitative phase analysis. SFCA and SFCA-I phases are the key bonding materials in iron ore sinter, and improved understanding of the effects of processing parameters such as basicity on their formation and decomposition may assist in improving efficiency of industrial iron ore sintering operations. Increasing basicity significantly increased the thermal range of SFCA-I, from 1363 K to 1533 K (1090 °C to 1260 °C) for a mixture with B = 2.48, to ~1339 K to 1535 K (1066 °C to 1262 °C) for a mixture with B = 3.96, and to ~1323 K to 1593 K (1050 °C to 1320 °C) at B = 4.94. Increasing basicity also increased the amount of SFCA-I formed, from 18 wt pct for the mixture with B = 2.48 to 25 wt pct for the B = 4.94 mixture. Higher basicity of the starting sinter mixture will, therefore, increase the amount of SFCA-I, considered to be more desirable of the two phases. Basicity did not appear to significantly influence the formation mechanism of SFCA-I. It did, however, affect the formation mechanism of SFCA, with the decomposition of SFCA-I coinciding with the formation of a significant amount of additional SFCA in the B = 2.48 and 3.96 mixtures but only a minor amount in the highest basicity mixture. In situ neutron diffraction enabled characterization of the behavior of magnetite after melting of SFCA produced a magnetite plus melt phase assemblage.

  8. Evaporation residue cross-section in the decay of 254No* formed in 206Pb + 48Ca and its isotopic dependence using other Pb targets within the dynamical cluster-decay model

    NASA Astrophysics Data System (ADS)

    Niyti; Gupta, Raj K.; Hess, Peter Otto

    2015-06-01

    The dynamical cluster-decay model (DCM), with deformation and orientation effects included, is used to calculate the fusion evaporation residue cross-sections σxn for x = 1, 2, 3 and 4 neutrons emission in a fusion reaction 206Pb + 48Ca → 254No* at various 48Ca-beam energies Elab = 212.7- 242.5 MeV (equivalently, E* = 19.8- 43.9 MeV). Considering the higher multipole deformations up to hexadecapole deformation β4i and the sticking moment-of-inertia IS, the DCM with pocket formula for nuclear proximity potential is shown to give a good description of the measured individual light-particle (here neutrons) decay channels for configurations of "hot, compact" orientations θci, within one parameter fitting of the neck-length ΔR. A check on some of the variables involved in DCM shows that (i) spherical configurations give nearly the same result as above for deformed and oriented ones; (ii) the non-sticking moment-of-inertia INS gives unphysical results; and (iii) configurations of "cold, elongated" orientations do not fit the data at all. Furthermore, for the four different isotopes of 204,206,207,208Pb-based reactions, the dependence of, say, the 2n-emission yield σ2n on the isotopic composition of the compound nucleus is also studied within the DCM for "hot" fusion process. Of all the four Pb-isotopes and three excitation energies E* considered, at each E*, the ΔR is largest for compound system 256No*, followed by 255No*, 254No* and smallest for 252No*, which means to suggest that the neutrons emission occur earliest for 256No*, then for 255No*, 254No* and finally by 252No*, in complete agreement with experimental data according to which compound system 256No* has the highest cross-section and 252No* the lowest with 255No* and 254No* lying in between. This result is related to the double magicity of both the target (208Pb) and projectile (48Ca) nuclei, as well as to the experimentally known result of projectile with a larger number of neutrons (here the target

  9. Correlated Nd, Sr and Pb isotope variation in Walvis Ridge basalts and implications for the evolution of their mantle source

    NASA Astrophysics Data System (ADS)

    Richardson, S. H.; Erlank, A. J.; Duncan, A. R.; Reid, D. L.

    1982-07-01

    Basement intersected in DSDP holes 525A, 528 and 527 on the Walvis Ridge consists of submarine basalt flows and pillows with minor intercalated sediments. These holes are situated on the crest and mid and lower northwest flank of a NNW-SSE-trending ridge block which would have closely paralleled the paleo mid-ocean ridge [13, 14]. The basalts were erupted approximately 70 m.y. ago, an age equivalent to that of immediately adjacent oceanic crust in the Angola Basin and consistent with formation at the paleo mid-ocean ridge [14]. The basalt types vary from aphyric quartz tholeiites on the ridge crest to highly plagioclase phyric olivine tholeiites on the ridge flank. These show systematic differences in incompatible trace element and isotopic composition. Many element and isotope ratio pairs form systematic trends with the ridge crest basalts at one end and the highly phyric ridge flank basalts at the other. The low 143Nd/ 144Nd (0.51238), 206Pb/ 204Pb (17.54), 208Pb/ 204Pb (15.47), 208Pb/ 204Pb (38.14) and high 87Sr/ 86Sr (0.70512) ratios of the ridge crest basalts suggest derivation from an old Nd/Sm-, Rb/Sr- and Pb/U-enriched mantle source. This isotopic signature is similar to that of alkaline basalts on Tristan de Cunha but offset to significantly lower Nd and Pb isotopic ratios. The isotopic ratio trends may be extrapolated beyond the ridge flank basalts with higher 143Nd/ 144Nd (0.51270), 206Pb/ 204Pb (18.32), 207Pb/ 204Pb (15.52), 208Pb/ 204Pb (38.77) and lower 87Sr/ 86Sr (0.70417) ratios in the direction of increasingly Nd/Sm-, Rb/Sr- and Pb/U-depleted source compositions. These isotopic correlations are equally consistent with mixing od depleted and enriched end member melts or partial melting of an inhomogenous, variably enriched mantle source. However, observe Zr sbnd Ba sbnd Nb sbnd Y interelement relationships are inconsistent with any simple two-component model of magma mixing, as might result from the rise of a lower mantle plume through the upper

  10. Australia and Indonesia in collision: geochemical sources of magmatism

    NASA Astrophysics Data System (ADS)

    Elburg, M. A.; Foden, J. D.; van Bergen, M. J.; Zulkarnain, I.

    2005-01-01

    The islands of Alor, Lirang, Wetar and Romang are located in the extinct section of the Sunda-Banda arc, where the collision with the Australian continent has brought subduction to a halt. Intrusive and extrusive igneous samples show a wide range of Sr, Nd and Pb isotopic characteristics. Samples from the northeast coast of Alor extend the trend of increasing 206Pb/ 204Pb ratios along the arc in an easterly direction, with values as high as 19.6. Samples from Alor's south coast, Lirang, Wetar and Romang have appreciably lower 206Pb/ 204Pb ratios (≤19.1), and 143Nd/ 144Nd ratios down to 0.5119. The Pb isotope data are interpreted as reflecting mixing between two internally variable end members within the subducting Australian continent, either the upper and lower crust, or two upper crustal end members of different ages. These melts may come up virtually unmodified, giving rise to the felsic, low 143Nd/ 144Nd samples, or may interact with the mantle, of which the partial melts and the fractionation products thereof give rise to basalts to rhyodacites with more intermediate Nd isotopic characteristics. Mixing modelling of the latter samples' isotopic ratios constrains the amount of crustal material that has been added to the mantle wedge to reach up to 9%. The isotopic and trace element heterogeneity in the samples studied is likely to reflect inhomogeneity of the crustal sources contributing to magmatism.

  11. Dust Deposition and Migration of the ITCZ through the Last Glacial Cycle in the Central Equatorial Pacific (Line Islands).

    NASA Astrophysics Data System (ADS)

    Reimi Sipala, M. A.; Marcantonio, F.

    2014-12-01

    Atmospheric dust can be used to record climate change in addition to itself playing a role in several key climate processes, such as affecting Earth's albedo, fomenting rain coalescence, encouraging biological productivity, and enhancing carbon export though particle sinks. Using deep sea sediments, it is possible to quantify and locate the sources and sinks of atmospheric dust. A key area of research is the shift in the inter-tropical converge zone (ITCZ), a thermally influenced area that shifts according to the northern and southern hemisphere temperature gradient. This ongoing project focuses on the changes of the ITCZ over the Central Equatorial Pacific (CEP) over the past ~25000 years. The research focuses on two cores taken from the Line Islands Ridge at 0° 29' N (ML1208-18GC), and 4° 41' N (ML1208-31BB). The main aim is to quantify the magnitude and provenance of windblown dust deposited in the CEP, and to address questions regarding the nature of the variations of dust through ice-age climate transitions. Radiogenic isotopes (Sr, Nd, Pb) have been successfully used to distinguish between different potential dust sources in the aluminosilicates fractions of Pacific Sediments. Our preliminary Pb isotope ratios suggest that, for modern deposition, the northern core's (31BB) detrital sediment fraction is likely sourced from Asian Loess (average ratios are 206Pb/204Pb = 18.88, 207Pb/204Pb = 15.69, 208Pb/204Pb = 39.06). The equatorial core's (18GC) detrital fraction has a less radiogenic Pb signature, which is consistent with South American dust sourcing (206Pb/204Pb = 18.62, 207Pb/204Pb = 15.63, 208Pb/204Pb = 38.62). This is indicative of a strong modern ITCZ that acts as an effective barrier for inter-hemispheric dust transport. Prior to Holocene time, the changes in Pb isotope ratios in both cores appear to be in anti-phase; the northern core becomes less radiogenic up to the LGM, while the southern core becomes more radiogenic. This is potentially due to a

  12. The lead isotope systematics of ophiolite complexes

    NASA Astrophysics Data System (ADS)

    Hamelin, Bruno; Dupré, Bernard; Allègre, Claude J.

    1984-03-01

    Samples of eleven ophiolites from the Mediterranean and the Pacific belts have been studied through Pb sbnd Pb systematics. The ophiolites studied show both isotopic variations within one sequence and differences between the various complexes. The intra-sequence isotopic variations result principally from the in situ decay of uranium and thorium since the formation of the ophiolites. μ ratios ( 238U/ 204Pb ) higher than 50 in the effusive part of ophiolites are required to explain the 206Pb/ 204Pb spread within the sequences, and such values are notably higher than those presently measured in the oceanic crust. This uranium enrichment with respect to lead is due to the combined effect of the magmatic fractionations and of chemical exchanges during marine alteration. Pb loss must be an important factor for the U/Pb increase. Since the 207Pb/ 204Pb ratio is not affected by recent radioactive decay, it represents a very useful tracer for the discussion of the genetic environment of the ophiolites. Three main types of Pb isotopic characteristics may be distinguished among ophiolite complexes, on the basis of their 207Pb/ 204Pb : - The ophiolite complexes of In Zecca (Corsica), Semail (Oman) and Toba (Japan) show 207Pb/ 204Pb similar to the least radiogenic present-day MORB. These complexes probably originated in regions geochemically comparable to the present-day depleted mantle. However, the Semail ophiolite has a higher 208Pb/ 204Pb ratio than MORB, which may be compatible with an origin in an interarc basin or premature arc. - The circum-Pacific ophiolites of Papua New Guinea, New Caledonia and Zambales (Philippines) have 207Pb/ 204Pb comparable to the present-day "transitional" portions of the ridges. - Finally the circum-Mediterranean ophiolites of Troodos, Vourinos, and Antalya, display 207Pb/ 204Pb ratios clearly higher than those of the present accretion zones. Thus, their genesis must have involved a significant continental component, and an origin in an

  13. Lead Isotopic Compositions of the Endeavour Sulfides, Juan de Fuca Ridge

    NASA Astrophysics Data System (ADS)

    Labonte, F.; Hannington, M. D.; Cousens, B. L.; Blenkinsop, J.; Gill, J. B.; Kelley, D. S.; Lilley, M. D.; Delaney, J. R.

    2006-12-01

    32 sulfide samples from the main structures of the Endeavour vent field, Juan de Fuca Ridge, were analyzed for their Pb isotope composition. The samples were collected from 6 main vent fields between 1985 and 2005 and encompass a strike length of more than 15 km along the ridge crest. The sulfides are typical of black smoker deposits on sediment-starved mid-ocean ridges. Pb isotope compositions of the massive sulfides within the six hydrothermal fields vary within narrow ranges, with 206Pb/204Pb = 18.58 18.75, 207Pb/204Pb = 15.45 15.53 and 208Pb/204Pb = 37.84 38.10. A geographic trend is observed, with the lower Pb ratios restricted mostly to the northern part of the segment (Salty Dawg, Sasquatch and High Rise fields), and the higher Pb ratios restricted mostly to the southern part of the segment (Main Endeavour, Clam Bed and Mothra fields). Variations within individual fields are much smaller than those between fields, and variation within individual sulfide structures is within the uncertainty of the measurements. Therefore, it is unlikely that the ranges of Pb isotope compositions along the length of the segment reflect remobilization, replacement, and recrystallization of sulfides, as suggested for the observed Pb isotope variability in some large seafloor sulfide deposits. Instead, the differences in isotopic compositions from north to south are interpreted to reflect differences in the source rocks exposed to hydrothermal circulation of fluids below the seafloor. Possible sources of the somewhat more radiogenic Pb may be small amounts of buried sediment, either from turbidites or from hemipelagic sediment. This possibility is supported by high concentrations of CH4 and NHC4 found in the high-temperature vent fluids at the Main Endeavour Field, which are interpreted to reflect subseafloor interaction between hydrothermal fluids and organic material in buried sediments. However, the majority of the samples fall below and are approximately parallel to the

  14. Sr-Nd-Pb isotope systematics and clinopyroxene-host disequilibrium in ultra-potassic magmas from Toro-Ankole and Virunga, East-African Rift: Implications for magma mixing and source heterogeneity

    NASA Astrophysics Data System (ADS)

    Muravyeva, N. S.; Belyatsky, B. V.; Senin, V. G.; Ivanov, A. V.

    2014-12-01

    Nd, Pb and Sr isotope ratios have been determined for kamafugite lava and clinopyroxene phenocrysts from Bunyaruguru (Toro-Ankole) and Virunga volcanic fields of the East African Rift. The whole rock Sr-Nd isotopic signatures of kamafugites (87Sr/86Sr: 0.70463-0.70536; 143Nd/144Nd: 0.51249-0.51255) suggest derivation from an EM1-type mantle source. In contrast, Pb isotopic compositions of the same samples (206Pb/204Pb: 19.00-19.57; 207Pb/204Pb: 15.69-15.74; 208Pb/204Pb: 39.30-40.26) reveal a similarity to EM2-type mantle. New Nd, Pb and Sr isotopic data for clinopyroxene (87Sr/86Sr: 0.70473-0.70503; 143Nd/144Nd: 0.51250-0.51254; 206Pb/204Pb: 18.04-18.17; 207Pb/204Pb: 15.58-15.60; 208Pb/204Pb: 38.09-38.23) suggest derivation from an EM1-like source, and indicate Sr and Pb isotope disequilibrium between clinopyroxene and corresponding host rock. Moreover, clinopyroxenes exhibiting a greater degree of isotopic disequilibrium with their host rock are more sodic in composition. The isotopic disequilibrium is corroborated by the presence of chemical zoning within clinopyroxene, which suggests rapid magma ascent rates preventing melt homogenization. The Pb isotopic ratios for both mineral and corresponding whole rock, together with published data on East African rift-related alkaline centers, define a trend interpreted to represent a mixing line for melts derived from sources such as EM1 and as HIMU. The similar isotopic compositions for clinopyroxene from the different volcanic rocks within the East African Rift suggest the existence of a common, older mantle source for their parental melts. The origin of these melts can be attributed to an enrichment event ~ 400-500 Ma, i.e., significantly prior the younger ultrapotassic magmatism. Our preferred interpretation for the results reported here involves the mixing of melts derived from EM1- and HIMU-like sources, which were rapidly transported to the Earth's surface. The primary magmas formed as the result of melting of a

  15. Inter-Tropical Convergence Zone Shifts During the Last Glacial Cycle Near the Line Islands Ridge.

    NASA Astrophysics Data System (ADS)

    Reimi Sipala, M. A.; Marcantonio, F.

    2015-12-01

    This research focuses on the shift in the inter-tropical convergence zone (ITCZ) during the last glacial cycle. Deep sea sediments from the Central Equatorial Pacific (CEP) are used to quantify and isolate the sources and sinks of atmospheric dust. Dust records and influences climate affecting a wide range of process from Earth's Albedo to carbon export. Our aim is to determine the provenance of windblown dust deposited in the CEP near the Line Islands Ridge using radiogenic Nd and Pb isotopes, and to infer the location of the ITCZ and the changes of atmospheric transport through ice-age climate transitions. We focus on three cores from the CEP, along a meridional transect at approximately 160° W --- 0° 28' N (ML1208-17PC), 4° 41' N (ML1208-31BB), and 7 ° 2'N (ML1208-31BB). Radiogenic isotopes (Sr, Nd, Pb) have been successfully used to distinguish between different potential dust sources in the aluminosilicates fractions of Pacific Sediments. Our preliminary data suggest that the equatorial core (17PC) predominantly receives its dust from South America and South American volcanics South America (206Pb/204Pb = 18.62, 207Pb/204Pb = 15.63, 208Pb/204Pb = 38.62; ; ɛNd = ~ -5). The middle core, which more closely reflects the modern position of the ITCZ, has varied dust provenance through time, at times consistent with Asian Loess (average ratios are 206Pb/204Pb = 18.88, 207Pb/204Pb = 15.69, 208Pb/204Pb = 39.06; ɛNd = ~ -7) and Asian Volcanics (ɛNd = ~-1) suggesting a shift in the ITCZ south of 4N before the LGM. Our results for the most northern core are forthcoming. Prior to Holocene time, the changes in Pb isotope ratios in both cores appear to be in anti-phase; the northern core becomes less radiogenic up to the LGM, while the southern core becomes more radiogenic. This is potentially due to a weakening of the ITCZ during glacial times. A secondary aim of this work is to determine if the ITCZ migrated further south than core 17PC during Heinrich stage II.

  16. Clinopyroxene-host disequilibrium (Sr-Nd-Pb isotope systematics) in ultra-potassic magmas from East-African Rift: Implications for magma mixing and source heterogeneity

    NASA Astrophysics Data System (ADS)

    Muravyeva, Natalya; Belyatsky, Boris; Senin, Valeriy

    2014-05-01

    Nd, Pb and Sr isotope ratios have been determined for kamafugite lava and clinopyroxene and phlogopite phenocrysts from Toro-Ankole and Virunga volcanic fields of the East African Rift. The whole rock Sr - Nd isotopic signatures of kamafugites (87Sr/86Sr: 0.70463 - 0.70536; 143Nd/144Nd: 0.51249 - 0.51255) suggest derivation from an EM1-type mantle source. In contrast, Pb isotopic compositions of the same samples (206Pb/204Pb: 19.00 - 19.57; 207Pb/204Pb: 15.69 - 15.74; 208Pb/204Pb: 39.30 - 40.26) reveal a similarity to EM2-type mantle. New Nd, Pb and Sr isotopic data for clinopyroxene (87Sr/86Sr: 0.70473 - 0.70503; 143Nd/144Nd: 0.51250 - 0.51254; 206Pb/204Pb: 18.04 - 18.17; 207Pb/204Pb: 15.58 - 15.60; 208Pb/204Pb: 38.09 - 38.23) suggest derivation from an EM1-like source, and indicate Sr and Pb isotope disequilibrium between clinopyroxene and corresponding host rock. Moreover, clinopyroxenes demonstrating a greater degree of isotopic disequilibrium with their host rock are more sodic in composition. The isotopic disequilibrium is corroborated by the presence of chemical zoning within clinopyroxene, which suggests rapid magma ascent rates preventing melt homogenization. The Pb isotopic ratios for both mineral and corresponding whole rock, together with published data on East African rift-related alkaline centers, define a trend interpreted to represent a mixing line for melts derived from sources such as EM1 and as HIMU. The similar isotopic compositions for clinopyroxene from the different volcanic rocks within the East African Rift suggest the existence of a common, older mantle source for their parental melts. The origin of these melts can be attributed to an enrichment event ~ 400-500 Ma, i.e., significantly prior the younger (Quaternary) ultrapotassic magmatism. Our preferred interpretation for the results reported here involves the mixing of the melts derived from EM1- and HIMU-like sources, which were rapidly transported to the Earth's surface. The primary

  17. Metals and isotopes in Juan de Fuca Ridge hydrothermal fluids and their associated solid materials

    SciTech Connect

    Hinkley, T.K.; Tatsumoto, M.

    1987-10-10

    The /sup 87/Sr//sup 86/Sr ratio of the hydrothermal solution (HTS) (0.7034) is larger than that of basalt (0.7025) at the southern vent field of the Juan de Fuca Ridge (SJFR). Both the Sr isotopic ratio for HTS and the water/rock interaction ratio lie between those at two sites farther south on the East Pacific Rise, 13 /sup 0/N and 21 /sup 0/N. These parameters may be closely related to subsurface temperatures and rates of magma ascent and to extent of faulting and surface areas of the frameworks of the hydrothermal systems. For these three Pacific Ocean sites there is no steady geographical progression of these measured parameters, nor of reported spreading rate, with increasing latitude northward. Pb and Nd isotopic measurements are uniform for all samples from the SJFR, ranging only from 18.43 to 18.58 for /sup 206/Pb//sup 204/Pb (fluids and associated solids) and centering near 0.5131 for /sup 143/Nd//sup 144/Nd (only fluids measured). Values for basalts and sulfides from the site have similar values. Relatively high /sup 206/Pb//sup 204/Pb values at the SJFR suggest the potential for the existence of an anomalous radiogenic heat source in the underlying mantle material.

  18. Trace-element and Sr, Nd, Pb, and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

    USGS Publications Warehouse

    Stern, C.R.; Frey, F.A.; Futa, K.; Zartman, R.E.; Peng, Z.; Kurtis, Kyser T.

    1990-01-01

    The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The "cratonic" basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in 87Sr/86Sr (0.70316 to 0.70512), 143Nd/144Nd (e{open}Nd) and 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the "cratonic" basalts. In contrast, the "transitional" basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by 87Sr/86Sr=0.7039??0.0004, e{open}Nd, 206Pb/204Pb=18.60??0.08, 207Pb/204Pb=15.60??0.01, and 208Pb/204Pb=38.50??0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the "cratonic" basalts, are displaced to higher 87Sr/86Sr at a given 143Nd/144Nd and to higher 207Pb/204Pb at a given 208Pb/204Pb. The "transitional" basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the "cratonic" and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ??18O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ??18O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ??18O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc

  19. Radiogenic Isotopes As Paleoceanographic Tracers in Deep-Sea Corals: Advances in TIMS Measurements of Pb Isotopes and Application to Southern Ocean Corals

    NASA Astrophysics Data System (ADS)

    Wilson, D. J.; van de Flierdt, T.; Bridgestock, L. J.; Paul, M.; Rehkamper, M.; Robinson, L. F.; Adkins, J. F.

    2014-12-01

    Deep-sea corals have emerged as a valuable archive of deep ocean paleoceanographic change, with uranium-series dating providing absolute ages and the potential for centennial resolution. In combination with measurements of radiocarbon, neodymium isotopes and clumped isotopes, this archive has recently been exploited to reconstruct changes in ventilation, water mass sourcing and temperature in relation to millennial climate change. Lead (Pb) isotopes in both corals and seawater have also been used to track anthropogenic inputs through space and time and to trace transport pathways within the oceans. Better understanding of the oceanic Pb cycle is emerging from the GEOTRACES programme. However, while Pb isotopes have been widely used in environmental studies, their full potential as a (pre-anthropogenic) paleoceanographic tracer remains to be exploited. In deep-sea corals, challenges exist from low Pb concentrations in aragonite in comparison to secondary coatings, the potential for contamination, and the efficient elemental separation required for measurement by thermal ionisation mass spectrometry (TIMS). Here we discuss progress in measuring Pb isotopes in coral aragonite using a 207Pb-204Pb double spike on a ThermoFinnigan Triton TIMS. For a 2 ng NIST-981 Pb standard, the long term reproducibility (using 1011 Ω resistors) is ~1000 ppm (2 s.d.) on 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios. We now show that using a new 1012 Ω resistor to measure the small 204Pb beam improves the internal precision on these ratios from ~500 ppm (2 s.e.) to ~250 ppm (2 s.e.) and we envisage a potential improvement in the long term reproducibility as a consequence. We further assess the internal precision and external reproducibility of our method using a BCR-2 rock standard and an in-house coral standard. Preliminary evidence on the application of this method to natural samples is derived from cleaning experiments and replication tests on deep-sea corals from the Southern

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

    PubMed

    Álvarez-Iglesias, P; Rubio, B; Millos, J

    2012-10-15

    San Simón Bay, the inner part of the Ría 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 (206)Pb/(207)Pb, (206)Pb/(204)Pb, (207)Pb/(204)Pb, (208)Pb/(204)Pb and (208)Pb/(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.

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

    NASA Astrophysics Data System (ADS)

    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

  2. The effect of exposure to employees from mining and milling operations in a uranium mine on lead isotopes--a pilot study.

    PubMed

    Gulson, Brian L; Mizon, Karen J; Dickson, Bruce L; Korsch, Michael J

    2005-03-01

    Potential exposure during mining and milling of uranium ore has resulted in the industry being highly regulated. Exposure can arise from inhalation of the daughter product radioactive gas radon (222Rn), inhalation of radioactive dust particles from mining and milling, direct irradiation from outside the body, and ingestion of radionuclides (e.g. uranium or radium) in food or water. Making use of the highly unusual lead isotopic signature for uranium ores (high 206Pb/204Pb from the high uranium content, low 208Pb/204Pb from the low Th/U ratio), we undertook a pilot study of nine male mine employees and three controls from the Ranger uranium mine in the Northern Territory Australia to determine if it was feasible to use lead isotopes in blood to identify exposure to uranium-derived materials. The lead isotopic data for the mine employees and controls plot in two distinct fields which are consistent with predicted isotopic patterns. Assuming retention of 10% of the ingested lead, then the increases seen in 206Pb represent intakes of between 0.9 and 15 mg, integrated over the years of exposure. The small amount of lead does not affect blood lead concentrations, but appears to be sufficient to be detectable with sensitive isotopic methods. Further studies, including those on urine, should be undertaken to confirm the veracity of the lead isotope method in monitoring exposure of uranium industry employees.

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

    NASA Astrophysics Data System (ADS)

    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.

  4. Source and distribution of lead in the surface sediments from the South China Sea as derived from Pb isotopes.

    PubMed

    Zhu, Laimin; Guo, Laodong; Gao, Ziyou; Yin, Guan; Lee, Ben; Wang, Fei; Xu, Jiang

    2010-11-01

    Rapid economic development in East Asian countries has inevitably resulted in environmental degradation in the surrounding seas, and concern for the environment and its protection against pollutants is increasing. Identification of sources of contaminants and evaluation of current environmental status are essential to environmental pollution management, but relatively little has been done in the South China Sea (SCS). In order to investigate the abundance, distribution, and sources of Pb within the SCS, stable Pb isotopes and their ratios were employed to assess the contamination status and to differentiate between natural and anthropogenic origins of Pb in the surface sediments. The total Pb concentrations in sediments varied from 4.18 to 58.7 mg kg(-1), with an average concentration of 23.6 ± 8.9 mg kg(-1). The observed Pb isotope ratios varied from 18.039 to 19.211 for (206)Pb/(204)Pb, 15.228 to 16.080 for (207)Pb/(204)Pb, 37.786 to 39.951 for (208)Pb/(204)Pb, 1.176 to 1.235 for (206)Pb/(207)Pb, and 2.468 to 2.521 for (208)Pb/(207)Pb. The majority of these ratios are similar to those reported for natural detrital materials. Combined with Pb enrichment factor values, our results show that Pb found within most of the SCS sediments was mainly derived from natural sources, and that there was not significant Pb pollution from anthropogenic sources before 1998. Further studies are needed to reconstruct deposition history and for trend analysis.

  5. Isotopic Studies of the Guerrero Composite Terrane, West-Central Mexico: Implications for Provenance of Crustal Rocks and Ore Metals

    NASA Astrophysics Data System (ADS)

    Potra, A.; Macfarlane, A. W.; Salters, V. J.; Sachi-Kocher, A.

    2010-12-01

    New Pb, Sr, and Nd isotope analyses of various crustal units and ores from the Guerrero terrane are presented in order to gain insight into their provenance. Mesozoic basement rocks from the Arteaga Complex and Tejupilco metamorphic suite contain radiogenic Pb relative to bulk earth models (206Pb/204Pb between 18.701 and 19.256, 207Pb/204Pb between 15.623 and 15.693, and 208Pb/204Pb between 38.694 and 39.216), plotting to the right of the average Pb crust evolution curve of Stacey and Kramers (1975). The isotopic compositions of Pb in these rocks are substantially more radiogenic than published data on high-grade metamorphic rocks from the Grenvillian-age Oaxaca terrane, but are similar to Paleozoic basement rocks of the Mixteca terrane. Sr and Nd isotope data suggest that the basement rocks of the Guerrero terrane partly originated from ocean-floor rocks which were overlain by sediments derived from a cratonic terrane, possibly represented by the metamorphic complexes of the Oaxaca or Mixteca terranes. Lead isotope ratios of Cretaceous sedimentary rocks of the Zihuatanejo and Huetamo Sequences define two different clusters, with the Zihuatanejo Sequence units shifted to more radiogenic values (206Pb/204 between 18.763 and 19.437, 207Pb/204Pb between 15.580 and 15.643, and 208Pb/204Pb between 38.510 and 38.892). Samples from the Huetamo Sequence are less radiogenic than the metamorphic basement, with Pb isotope ratios between 18.630 and 18.998 for 206Pb/204, 15.563 and 15.641 for 207Pb/204Pb, and 38.369 and 38.610 for 208Pb/204Pb. They plot close to the radiogenic end of the MORB field, suggesting a possible mixing line between the basement rocks and the MORB component. Lead isotope ratios of Tertiary intrusive rocks from La Verde, El Malacate, and La Esmeralda resemble the orogene reservoir in the plumbotectonics model of Zartman and Doe (1981). Plutonic rocks from La Verde show the most radiogenic Pb compositions, suggesting a significant influence of old

  6. Geochemistry of ultrapotassic volcanic rocks in Xiaogulihe NE China: Implications for the role of ancient subducted sediments

    NASA Astrophysics Data System (ADS)

    Sun, Yang; Ying, Jifeng; Zhou, Xinhua; Shao, Ji'an; Chu, Zhuyin; Su, Benxun

    2014-11-01

    The unique eruptions of ultrapotassic volcanic rocks in eastern China reported so far took place in the Xiaogulihe area of western Heilongjiang Province, NE China. These ultrapotassic rocks are characterized by extremely high K2O contents (> 7 wt.%), abnormally unradiogenic Pb isotopic compositions (206Pb/204Pb = 16.44-16.55; 207Pb/204Pb = 15.39-15.46; 208Pb/204Pb = 36.35-36.61), and moderately high 87Sr/86Sr ratios (0.7053-0.7057), which can be basically correlated with those of ultrapotassic igneous rocks distributed widely in northwestern America and Aldan Shield. The positive correlation between 187Os/188Os and 1/Os argues that these ultrapotassic rocks have probably experienced negligible lower continental crust addition (less than 1%) during magma ascent. The high contents of K2O and negative correlation between 87Sr/86Sr and 206Pb/204Pb of these ultrapotassic rocks indicate the presence of a potassic phase, mostly phlogopite, in their mantle source. Their strong fractionation of rare earth elements and lack of Nd-Hf isotopic decoupling reveal a low-degree partial melting of garnet-bearing source rocks. In addition, the low CaO and Al2O3 contents of whole-rock compositions and low Fe/Mn ratios of olivine phenocryst chemistries suggest peridotites rather than pyroxenites as dominant source rocks for the Xiaogulihe ultrapotassic rocks. Based on these distinctive geochemical characteristics, we thus propose that the ultimate mantle source of the Xiaogulihe ultrapotassic volcanic rocks is phlogopite-bearing garnet peridotite within the lower part of the sub-continental lithospheric mantle (SCLM) that had been metasomatized by potassium-rich silicate melts. Combined with the unradiogenic Pb compositions, the most likely source of these potassium-rich silicate melts is the ancient subducted continental-derived sediments (> 1.5 Ga). These ancient subducted sediments, possessing relatively low initial Pb isotopic compositions, had experienced large U/Pb fractionation

  7. Spatial and temporal evolution of lead isotope ratios in the North Atlantic Ocean between 1981 and 1989

    NASA Astrophysics Data System (ADS)

    Weiss, Dominik; Boyle, Edward A.; Wu, Jingfeng; Chavagnac, ValéRie; Michel, Anna; Reuer, Matthew K.

    2003-10-01

    Lead concentrations and isotope ratios were measured in North Atlantic surface water samples collected in 1981 (29°-79°N, 6°E-49°W) and in 1989 (23°-39°N, 29°-68°W). In the early 1980s, 206Pb/207Pb ratios in the North African Basin averaged 1.193 ± 0.005 (1 σ). Similar radiogenic ratios within the level of analytical precision (average 0.29%) were found in the Labrador and Iceland Basins (1.198 ± 0.006) and in the Norwegian Sea (1.196 ± 0.008). These radiogenic mixed layer signatures along with atmospheric global lead emission patterns suggest that most North Atlantic lead in the early 1980s was derived from North American leaded gasoline. Samples in the East Iberian Basin near Portugal and France showed lower 206Pb/207Pb ratios, between 1.167 and 1.182, indicating a significant influence of less radiogenic atmospheric lead transported from Europe and possibly the influence of the Rio Tinto acid mine drainage very close to shore in the Gulf of Cadiz. [Pb] across the entire North Atlantic Basin ranged between 54 and 145 pmol/kg, with the lowest values (54-74 pmol/kg) found at high latitudes (>65°N). In the late 1980s, surface waters in the western subtropical North Atlantic (North American Basin/Sargasso Sea, >47°W) and in the eastern subtropical North Atlantic (North African Basin/Central Iberian Basin, <45°W) showed very similar 206Pb/207Pb signatures with little zonal variation, ranging from 1.177 to 1.192. Lead concentrations ranged between 47 and 137 pmol/kg, increasing slightly from west to east. South of 25°N in the equatorial North Atlantic, crossing the subtropical/tropical surface water boundary, the 206Pb/207Pb seawater signatures were significantly less radiogenic (1.170-1.175) and concentrations were lower (≤51 pmol/kg). This difference suggests a relative increase in the atmospheric lead supply from the western Mediterranean/North African continent via Trade Easterlies and illustrates the effective barrier between the subtropical

  8. Lead isotopes in lichen transplants around a Cu smelter in Russia determined by MC-ICP-MS reveal transient records of multiple sources.

    PubMed

    Spiro, B; Weiss, D J; Purvis, O W; Mikhailova, I; Williamson, B J; Coles, B J; Udachin, V

    2004-12-15

    Transplants of the lichen Hypogymnia physodes, which is relatively tolerant to SO2 and heavy metals, were deployed for 3 months over a 60 km long SW-NE transect centered on a highly polluting Cu smelter and its adjoining town of Karabash, southern Urals, Russia. The abundance of 206Pb, 207Pb, 208Pb, and 204Pb were determined by MC-ICP-MS. The measurement of 204Pb revealed critical features, which would otherwise remain concealed: (i) The precise isotope ratios referenced to 204Pb allowed several different sources to be resolved even within the small area covered: (a) the obvious pollutant source of the Karabash Cu smelter; (b) two dispersed sources, likely to include soil with lower and different contributions of thorogenic and uranogenic lead; and (c) one anthropogenic source with higher contribution of 235U derived Pb. (ii) In part of the transect, the Pb isotope composition changed while the Pb concentrations remained the same. This indicates that the Pb content of the transplantation material from the background site was largely replaced and that the transplants provide a transient record reflecting a continuous accumulation and loss of environmental Pb, probably mainly in the form of extracellular particles. Overall, the method of lichen transplantation coupled with Pb isotope ratio determinations proved effective in assessing the usefulness of lichens in biomonitoring and in resolving different sources of atmospheric deposition.

  9. Enriched Nd-Sr-Pb isotopic signatures in the Dovyren layered intrusion ( eastern Siberia, Russia): Evidence for source contamination by ancient upper-crustal material

    USGS Publications Warehouse

    Amelin, Yu. V.; Neymark, L.A.; Ritsk, E. Yu; Nemchin, A.A.

    1996-01-01

    Major- and trace-element concentrations and Nd-, Sr- and Pb-isotopic ratios are reported for the Dovyren layered mafic-ultramafic intrusion in the northern Baikal region, eastern Siberia. Sm-Nd internal isochrons for an olivine gabbro from the layered series and a gabbronorite from a sill at the bottom of the Dovyren intrusion yield ages of 673 ?? 22 and 707 ?? 40 Ma, respectively. Initial isotopic ratios: 87Sr/86Sr (673) from 0.7101 to 0.7135, ??Nd(673 Ma) from - 16.3 to - 14.1, 206Pb/204Pb from 16.80 to 17.14, 207Pb/204Pb from 15.477 to 15.501 and 208Pb/204Pb from 37.17 to 37.59, are similar to those of late Archean-early Proterozoic upper continental crust, but do not appear to be a result of wallrock assimilation in the magma chamber. These isotopic features, as well as high K, Rb and LREE and low Ti concentrations in the calculated composition of the Dovyren parental magma, may be explained by subduction of sediments derived from upper continental crust into depleted mantle and subsequent melting of the metasomatized peridotite.

  10. Two-types of Early Cretaceous adakitic porphyries from the Luxi terrane, eastern North China Block: Melting of subducted Paleo-Pacific slab and delaminated newly underplated lower crust

    NASA Astrophysics Data System (ADS)

    Wang, Hao; Xu, Zhaowen; Lu, Xiancai; Fu, Bin; Lu, Jianjun; Yang, Xiaonan; Zhao, Zengxia

    2016-01-01

    The origin and tectonic setting of Early Cretaceous adakitic rocks from the Luxi terrane in the eastern North China Block (NCB) remain debated. To resolve this issue, we determined whole-rock geochemistry, zircon U-Pb ages, and in situ Hf-O isotopes of the Mengyin and Liujing adakitic porphyries from the Luxi terrane. Zircon U-Pb dating results reveal that both the Mengyin and Liujing plutons were emplaced during the Early Cretaceous, with weighted mean 206Pb/238U ages of 130 ± 1 Ma (2σ) and 131 ± 2 Ma (2σ), respectively. In addition, abundant Neoarchean-Paleoproterozoic inherited zircon cores are identified in the Mengyin adakitic porphyry with 207Pb/206Pb ages ranging from 2.53 to 2.42 Ga. Rocks of both plutons are silicic (SiO2 = 65.4-70.2 wt.%), metaluminous, and alkaline in composition, comprising mainly quartz syenite porphyries. Samples from both plutons are enriched in large ion lithophile elements (LILEs) (e.g., Rb, Sr, and Ba), and light rare earth elements (LREEs), depleted in high field strength elements (HFSEs) (e.g., Nb, Ta, and Ti), and heavy rare earth elements (HREEs), and have either positive or no Eu anomalies. In addition, both adakitic porphyries have high Mg# values (51-64), high Sr and La contents, low Y and Yb contents, and high Sr/Y (Mengyin = 149-264; Liujing = 58-110) and (La/Yb)N (Mengyin = 32.4-45.3; Liujing = 43.8-53.1) ratios, similar to adakitic rocks worldwide. The Mengyin adakitic porphyry has higher whole-rock εNd(t) values (-5.8 to - 4.1), more radiogenic Pb [(206Pb/204Pb)i = 18.35-18.39, (207Pb/204Pb)i = 15.55-15.56, (208Pb/204Pb)i = 38.20-38.23], higher zircon rim εHf(t) values (+ 3.3 to + 8.8) and δ18O values (+ 6.5‰ to + 7.9‰), and lower (87Sr/86Sr)i ratios (0.7049-0.7050) than the Liujing adakitic porphyry [εNd(t) = - 12.4 to - 12.2, (206Pb/204Pb)i = 17.63-17.72, (207Pb/204Pb)i = 15.56-15.58, (208Pb/204Pb)i = 37.76-37.94, εHf(t) = - 14.8 to - 11.2, δ18O = + 5.9‰ to + 7.1‰, (87Sr/86Sr)i = 0.7090-0.7091]. The

  11. Sr sbnd Pb sbnd Nd isotopic evidence that both MORB and OIB sources contribute to oceanic island arc magmas in Fiji

    NASA Astrophysics Data System (ADS)

    Gill, James B.

    1984-06-01

    Twenty-eight new Pb, 20 Sr, and 9 Nd isotopic compositions are presented for 32 rocks and one galena from Fiji and the South Fiji (back-arc) Basin. The Fijian rocks range in age from 35 to < 0.1 m.y., and are taken from arc tholeiitic, calc-alkaline, trondjhemitic, shoshonitic, and alkali olivine basalt series, and from the hybrid basalts to dacites of Kadavu. They span both the subduction-related and rifting-related episodes of Fijian history. For at least 30 m.y., andesite-dominated volcanics with arc-like trace element characteristics (e.g. Rb/Zr,Ba/La,Sr/Nd,Pb/U,Ba/Th, and La/Nb ratios higher than in either OIB or MORB) were erupted in the oceanic Vitiaz island arc which included Fiji. During the initial 2/3 of this time, most rocks belonged to an island are tholeiitic series similar to MORB both in some trace element (e.g. K/Rb,La/Yb,Hf/Th, and Y/Zr) and isotope ratios (e.g. relatively high 143Nd/ 144Nd and low 206Pb/ 204Pb ). Nearly constant 207Pb/ 204Pb ratios therein are attributed to mixing between a sediment-contaminated MORB source component with low 206Pb/ 204Pb , and an OIB source component lying within the conventional Sr sbnd Nd sbnd Pb mantle array. In later calc-alkaline and shoshonitic series rocks, these same trace element and isotopic ratios are more like those of OIB. The change was not accompanied by an increase in 207Pb/ 204Pb or Cs/K, indeed, 207Pb/ 204Pb is closer to the mantle array in these later series. Consequently, the change indicates a greater contribution from OIB sources, rather than from recycled ocean crust. These interpretations require that both MORB and OIB sources coexist in the uppermost mantle above subducted lithosphere. Rifting-related volcanism in Fiji, which accompanied opening of the North Fiji and Lau Basins, has been basalt-dominated but was drawn initially (in the shoshonites and related rocks) from much the same mixture of sources that fed the older andesite-dominated calc-alkaline series. Relative to the calc

  12. Southern Cordilleran Basaltic Andesite suite, southern Chihuahua, Mexico: A link between Tertiary continental arc and flood basalt magmatism in the North America

    SciTech Connect

    Cameron, K. L.; Nimz, G. J.; Kuentz, D.; Niemeyer, S.; Gunn, S.

    1989-06-10

    Mid-Cenozoic orogenic andesites and ignimbrites of western Mexico, southwestern New Mexico, and Arizona are commonly capped by basaltic andesites, most from 29--20 Ma. We refer to these mafic lavas as the Southern Cordilleran Basaltic Andesite (SCORBA) suite, and they may constitute the most extensive Cenozoic basaltic suite in North America. The SCORBA suite has trace element and isotopic characteristics of orogenic (arc) rocks (i.g., Ba/Nb/gt/40), and silica content (53--56% SiO/sub 2/) like the Grande Ronde Basalt, which represents about 80% of the volume of the Columbia River Group. Geochemical and isotopic data are presented on SCORBA lavas and rare mafic lavas (PRE-SCORBA) interlayered with older ignimbrites from a 700-km-long NE-SW transect of southern Chihuahua, Mexico. SCORBA and PRE-SCORBA lavas with relatively low K/P (/lt/7) and differing Ba/Nd (50 versus 18) have similar isotopic compositions, arguing against their isotopic signatures being controlled by crustal assimilation. Along the entire length of the transect, the basaltic rocks have /var epsilon//sub Nd/ and /sup 87/Sr//sup 86/Sr near bulk Earth and /sup 206/Pb//sup 204/Pb and /sup 207/Pb//sup 204/Pb ratios that lie along a 1.7 Ga pseudoisochron. The Pb isotopic variation is geographically controlled, becoming more radiogenic from east to west, reflecting mixing in mantle source regions. The eastern mantle source has low/sup 206/Pb//sup 204/Pb and is a mixture of an enriched, enriched-mantle-like (EMI) component with one or more depleted components, which could include an intraplate component with relatively high Nb/Y (/gt/0.8).

  13. Some Pb and Sr isotopic measurements on eclogites from the Roberts Victor mine, South Africa

    USGS Publications Warehouse

    Manton, W.I.; Tatsumoto, M.

    1971-01-01

    Five nodules of eclogite, one nodule of garnet peridotite and one sample of kimberlite from the Roberts Victor mine were analyzed for concentrations of U, Th, Pb, Rb and Sr and isotopic compositions of Pb and Sr. In the eclogites, U content ranges from 0.09 to 0.26 ppm, Th from 0.35 to 1.1 ppm, Pb from 0.79 to 5.5 ppm, Rb from 2.1 to 28 ppm and Sr from 133 to 346 ppm; 206Pb/204Pb ratios range from 14.8 to 18.5, 207Pb/204Pb from 14.9 to 15.7, 208Pb/204Pb from 35.2 to 38.5. The garnet peridotite contains 0.22 ppm U, 0.97 ppm Th, 1.05 ppm Pb, 6.9 ppm Rb and 108 ppm Sr and the kimberlite contains 2.5 ppm U, 30 ppm Th, 37 ppm Pb, 113 ppm Rb and 2040 ppm Sr. The lead in the eclogites has two components, a lead pyroextractable at 1100-1200?? and a non-pyroextractable residual lead. In three of the eclogites, which are to some extent altered, a proportion of the pyroextractable lead may be contaminating lead from the kimberlite, but an altered kyanite eclogite does not appear to be contaminated by this same kimberlite. The pyroextractable lead from a less altered eclogite contains a much larger proportion of 206Pb. Compositions calculated for the residual leads vary greatly. In many of the pyroextraction runs the primary eclogitic phases disappeared and the new phases plagioclase, clinopyroxene and a magnetic iron compound were formed. Why part of the lead should have been retained by these new phases is not understood. ?? 1971.

  14. Isotopic and fluid-inclusion constraints on the formation of polymetallic vein deposits in the central Argentinian Patagonia

    NASA Astrophysics Data System (ADS)

    Dejonghe, Léon; Darras, Benoît; Hughes, Guillermo; Muchez, Philippe; Scoates, James S.; Weis, Dominique

    2002-03-01

    The lead isotope compositions of galena and the fluid-inclusion systematics of nine barite-bearing polymetallic (Au, Ag, Pb, Zn) deposits of the central Argentinian Patagonia (Chubut and Rio Negro provinces) have been investigated to constrain the compositions and sources of the mineralizing fluids. Most of the deposits occur as veins, with less common wall-rock disseminations and/or stockworks, and are low-sulfidation epithermal deposits hosted in Jurassic volcanic rocks. Fluid-inclusion homogenization temperatures (Th) from quartz and sphalerite from the deposits fall within the range of 100-300 °C, with the highest measured average temperatures for the most eastern deposits (Mina Angela - 298 °C; Cañadón Bagual - 343 °C). The salinities of the hydrothermal fluids at all deposits were low to moderate (≤10.4 equiv. wt% NaCl). Three groups of ore deposits can be defined on the basis of 206Pb/204Pb ratios for galena and these show a general decrease from west to east (from 18.506 to 18.000). The central Argentinian Patagonia deposits have distinctly less radiogenic lead isotope compositions than similar deposits from Peru and Chile, except for the porphyry copper deposits of central and southern Peru. Galena from the Mina Angela deposit is characterized by very low radiogenic lead isotope compositions (18.000<206Pb/204Pb<18.037 and 38.03<208Pb/204Pb<38.09) and reflects interaction with Precambrian basement. The geographic trend in lead isotope compositions of both galena and whole rocks indicates a crustal contribution which increases eastwards, also reflected in the strontium-neodymium isotope systematics of the host lavas. Finally, due to the lack of precise age determinations for the central Patagonian polymetallic deposits, a potential link with Andean porphyry copper systems remains an open question.

  15. Lead isotope profiling in dairy calves.

    PubMed

    Buchweitz, John; McClure-Brinton, Kimberly; Zyskowski, Justin; Stensen, Lauren; Lehner, Andreas

    2015-03-01

    Lead (Pb) is a common cause of heavy metal poisonings in cattle. Sources of Pb on farms include crankcase oil, machinery grease, batteries, plumbing, and paint chips. Consequently, consumption of Pb from these sources may negatively impact animal health and Pb may be inadvertently introduced into the food supply. Therefore, the scope of poisoning incidents must be clearly assessed and sources of intoxication identified and strategies to mitigate exposure evaluated and implemented to prevent future exposures. Stable isotope analysis by inductively-coupled plasma mass spectrometry (ICP-MS) has proven itself of value in forensic investigations. We report on the extension of Pb stable isotope analysis to bovine tissues and profile comparisons with paint chips and soils collected from an affected dairy farm to elucidate the primary source. Pb occurs naturally as four stable isotopes: (204)Pb, (206)Pb, (207)Pb, and (208)Pb. Herein a case is reported to illustrate the use of (207)Pb/(206)Pb and (208)Pb/(206)Pb ratios to link environmental sources of exposure with tissues from a poisoned animal. Chemical Pb profiling provides a valuable tool for field investigative approaches to Pb poisoning in production agriculture and is applicable to subclinical exposures.

  16. [Speciation analysis of lead and its isotopes in fine particulate matters in Beijing by ICP-MS].

    PubMed

    Chen, Xi; Wang, Xiao-Yan; Liu, Yang; Zhang, Jing-Hua; Liu, Jing-Xiu; Yan, Lai-Lai; Wang, Jing-Yu

    2009-02-01

    Fine particulate matters (PMZ2.5) collected in Beijing during a period from September 2005 to May 2006 were studied. Sequential extraction procedures were applied to divide the total lead into three fractions, i.e. water soluble, liposoluble and insoluble lead. Lead concentrations and their isotopes in each fraction were then determined by inductively coupled plasma mass spectrometry (ICP-MS). Lead standard reference GBW 09133 was used to investigate the accuracy of lead concentration determination and SRM 981 was used to correct the mass discrimination and instrumental drift. The obtained results showed that the analytical precision of lead isotope ratios for SRM 981 of seven repeat measurements at lead concentration of 10 ng x mL(-1) came to about 0.34, 0.27 and 0.24 percent for the 206 Pb/204 Pb, 206Pb/207 Pb and 206Pb/208 Pb ratios, respectively. In Beijing, the mass concentrations for PM2.5 and lead of ambient air were 125.556 and 0.5415 microg x m(-3) respectively for winter 2005, and 201.6 and 0.475 microg x m(-3) respectively for spring 2006 on average, resembling those published results. It was indicated that the lead in the PM2.5 existed mainly in insoluble form, which accounted for 78.99%, while water soluble lead and liposoluble lead amount were 20.69% and 0.32%, respectively. The mean values of 206Pb/207Pb ratio for water soluble species and insoluble species were 1.152 6 +/- 0.009 3 and 1.219 3 +/- 0.009 1 respectively, with a significant difference (Student's test; p < 0.01) statically. By comparing 206Pb/207Pb ratios between biological specimen and ambient air samples, the 206Pb/207Pb ratios in water soluble fraction coincided very well with those in adult blood, therefore, water soluble lead but not insoluble lead in PM2.5 may be the potential source of adults blood lead in Beijing. More attention should be paid to the effect of soluble lead in fine particle matters on human health.

  17. [Study on heavy metal contaminations and the sources of Pb pollution in Jinghai Bay using the stable isotope technique].

    PubMed

    Xu, Lin-Bo; Gao, Qin-Feng; Dong, Shuang-Lin; Liu, Jia; Fu, Xiu-Juan

    2013-02-01

    The concentrations of typical heavy metals including Cu, Hg, Pb, Zn, Mn, Cd, Cr and As in the surface sediment and suspended particulate matter (SPM) in Jinghai Bay, Rongcheng city were tested. The degree of heavy metal pollution in the surface sediment was assessed according to the national standard of marine sediment quality. The potential ecological risk (PER) of heavy metals to marine ecosystem in Jinghai Bay was assessed using PER coefficient and risk index. The results showed that the levels of heavy metals and PER in the surface sediments were low enough to meet the requirement of the first class of the sediment quality standards except the levels of Cu and Zn in the sampling site S2 and Cd in S3, S4, S5 and S6 which met the requirements of the second class of the sediment quality standards. The PER coefficients of heavy metals increased following the sequence of Zn < Cr < Pb < Cu < As ratios of 208Ph/204Pb, 207Pb/204Pb, 206Pb/204Pb and 206pb/207pb in surface sediment were more closely related to that of SPM. The ratio of 206pb/207Pb for both surface sediment and SPM was the lowest at the sampling site S2 and negatively correlated to the Pb concentration. The comparisons of Pb stable isotope ratio between the isotope ratios of natural and anthropogenic source showed that the Pb contamination was mainly derived from the human activities such as industrial discharges and leaded gasoline.

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

    NASA Astrophysics Data System (ADS)

    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

  19. Pb isotopic constraints on the formation of the Dikulushi Cu-Pb-Zn-Ag mineralisation, Kundelungu Plateau (Democratic Republic of Congo)

    NASA Astrophysics Data System (ADS)

    Haest, Maarten; Schneider, Jens; Cloquet, Christophe; Latruwe, Kris; Vanhaecke, Frank; Muchez, Philippe

    2010-04-01

    Base metal-Ag mineralisation at Dikulushi and in other deposits on the Kundelungu Plateau (Democratic Republic of Congo) developed during two episodes. Subeconomic Cu-Pb-Zn-Fe polysulphide ores were generated during the Lufilian Orogeny (c. 520 Ma ago) in a set of E-W- and NE-SW-oriented faults. Their lead has a relatively unradiogenic and internally inhomogeneous isotopic composition (206Pb/204Pb = 18.07-18.49), most likely generated by mixing of Pb from isotopically heterogeneous clastic sources. These sulphides were remobilised and enriched after the Lufilian Orogeny, along reactivated and newly formed NE-SW-oriented faults into a chalcocite-dominated Cu-Ag mineralisation of high economic interest. The chalcocite samples contain only trace amounts of lead and show mostly radiogenic Pb isotope signatures that fall along a linear trend in the 207Pb/204Pb vs. 206Pb/204Pb diagram (206Pb/204Pb = 18.66-23.65; 207Pb/204Pb = 15.72-16.02). These anomalous characteristics reflect a two-stage evolution involving admixture of both radiogenic lead and uranium during a young fluid event possibly c. 100 Ma ago. The Pb isotope systematics of local host rocks to mineralisation also indicate some comparable young disturbance of their U-Th-Pb systems, related to the same event. They could have provided Pb with sufficiently radiogenic compositions that was added to less radiogenic Pb remobilised from precursor Cu-Pb-Zn-Fe polysulphides, whereas the U most likely originated from external sources. Local metal sources are also suggested by the 208Pb/204Pb-206Pb/204Pb systematics of combined ore and rock lead, which indicate a pronounced and diversified lithological control of the immediate host rocks on the chalcocite-dominated Cu-Ag ores. The Pb isotope systematics of polysulphide mineralisation on the Kundelungu Plateau clearly record a diachronous evolution.

  20. Source components and magmatic processes in the genesis of Miocene to Quaternary lavas in western Turkey: constraints from HSE distribution and Hf-Pb-Os isotopes

    NASA Astrophysics Data System (ADS)

    Aldanmaz, Ercan; Pickard, Megan; Meisel, Thomas; Altunkaynak, Şafak; Sayıt, Kaan; Şen, Pınar; Hanan, Barry B.; Furman, Tanya

    2015-08-01

    Hf-Pb-Os isotope compositions and highly siderophile element (HSE) abundance variations are used to evaluate the mantle source characteristics and possible effects of differentiation processes in lavas from western Turkey, where the eruption of Late Miocene to Quaternary OIB-type intraplate mafic alkaline lavas followed pre-Middle Miocene convergent margin-type volcanism. Concentrations of Os, Ir, and Ru (IPGE) in the OIB-type intraplate lavas decrease with fractionation for primitive melts (MgO > 10 wt%), suggesting that these elements reside predominantly in olivine and associated HSE retaining trace phases and behave compatibly during olivine-dominated fractionation. Fractional crystallization trends indicate distinctly lower bulk partition coefficients for IPGE in more evolved lavas, possibly reflecting a change in the fractionating assemblages. Pd and Re in the primitive melts display negative correlations with MgO, demonstrating moderately incompatible behavior of these elements during fractionation, while the significantly scattered variation in Pt against MgO may indicate the effects of micronuggets of a Pt-rich alloy. Os-rich alkaline primary lavas (>50 ppt Os) exhibit a limited range of 187Os/188Os (0.1361-0.1404), with some xenolith-bearing lavas displaying depletions in 187Os/188Os (0.1131-0.1232), suggesting slight compositional modification of primitive melts through contamination with highly depleted, Os-rich mantle lithosphere. More radiogenic Os isotope ratios (187Os/188Os > 0.1954) in the evolved lavas reflect contamination of the magmas by high187Os/188Os crustal material during shallow differentiation. The OIB-type lavas show limited variations in Hf and Pb isotopes with 176Hf/177Hf = 0.282941-0.283051, 206Pb/204Pb = 18.683-19.091, 207Pb/204Pb = 15.579-15.646, 208Pb/204Pb = 38.550-38.993; 176Hf/177Hf ratios correlate negatively with 208Pb*/206Pb*, suggesting the effects of similar mantle processes on the evolution of time-integrated Th/U and Lu

  1. Lead isotope constraints on the origin of andesite and dacite magmas at Tungurahua volcano (Ecuador)

    NASA Astrophysics Data System (ADS)

    Nauret, Francois; Ancellin, Marie-Anne; Vlastelic, Ivan; Tournigand, Pierre-Yves; Samaniego, Pablo; Le Pennec, Jean Luc; Gannoun, Mouhcine; Hidalgo, Silvana; Schiano, Pierre

    2016-04-01

    Understanding the occurrence of large explosive eruptions involving silica-rich magmas at mostly andesitic volcanoes is crucial for volcanic hazard assessment Here we focus on the well-known active Tungurahua volcano (Ecuador), specifically its eruptive sequence for the last 3000 years BP, which are characterized by VEI 3 explosive events involving mostly homogeneous andesitic compositions (56-59 wt.% SiO2). However, some large eruptions (VEI ≥ 4) involving andesitic and dacitic magmas (up to 66 wt.% SiO2) also occur at 3000 BP, 1250 BP and 1886 AD. An additional outburst of siliceous magmas occurred during the last eruptive eruption of this volcano in 2006 [1]. Volcanic products at Tungurahua are described as been generated by a binary mixing between a silica-rich and a silica-poor end-member, but the origin of these components was not discussed [2]. Major, trace elements and Sr-Nd-Pb isotopes were used to investigate the genesis of the andesites and dacites. Andesites are heterogeneous in terms of Pb isotopes (206Pb/204Pb: 18.189-19.154, 207Pb/204Pb:15.658-15.696, 208Pb/204Pb: 38.752-38.918, 207Pb/206Pb: 0.8240-0.8275) but homogeneous in terms of major-trace element. Dacite are characterized by homogenous and low 207Pb/206Pb (0.8235±0.0001), very low Nb/U (1.97 to 4.49) and Ce/Pb (2.52-2.99) and high Th/La ratios (0.24 to 0.49). Triangular distribution of data in major element or trace element ratio vs. Pb isotopes plots suggests that at least three components control geochemical variability at Tungurahua. We interpret andesite compositions as reflecting mainly a deep mixture of two mantle components, with small addition of crustal material. We suggest that dacite results from a mixing between various andesite compositions and a larger amount of a contaminant derived from the volcanic basement of the Tungurahua made of late Cretaceous to Palaeogene oceanic plateau basalts and volcano-sedimentary rocks volcanic. Since andesite and dacite occur during the same

  2. The origin of the Line Islands: plate or plume controlled volcanism?

    NASA Astrophysics Data System (ADS)

    Storm, L. P.; Konter, J. G.; Koppers, A. A.

    2011-12-01

    foundation of the central and southern provinces is shallower than the regional seafloor, suggesting that the thickness of the lithosphere in these two provinces may have an influence on the chemical compositions of seamounts. A suite of samples, previously analyzed for 40Ar/39Ar age data, was processed for lead (Pb), neodymium (Nd), hafnium (Hf) and strontium (Sr) isotope measurements to investigate whether the Line Islands are caused by 4-5 concurrent plumes or a lithospherically controlled source. Pb isotope compositions define two distinct groups: (1) low 206Pb/204Pb and 207Pb/204Pb ratios, and (2) high 206Pb/204Pb and 207Pb/204Pb ratios. When Pb isotope compositions are considered in relation to their dredge locations, the two identified groups do not define age-progressive volcanic chains expected for a plume origin. Instead, high 206Pb/204Pb and 207Pb/204Pb samples are strictly limited between the Molokai and Clarion fracture zones, suggesting that ocean crust segmentation related to mid-ocean ridge spreading and adjustments in the Pacific-Phoenix-Farallon triple junction partly controlled the melt compositions. These results, therefore, suggest that this major volcanic chain was likely not plume-derived.

  3. On the recent enrichment of subcontinental lithosphere: A detailed UPb study of spinel lherzolite xenoliths, Yukon, Canada

    NASA Astrophysics Data System (ADS)

    Carignan, Jean; Ludden, John; Francis, Don

    1996-11-01

    Lead strontium, and osmium isotopic data have been obtained for whole rocks and mineral separates (olivine, orthopyroxene, clinopyroxene, and spinel) for spinel lherzolite xenoliths hosted by lavas of the Quaternary Alligator Lake volcanic centre, southern Yukon. Whole-rock xenolith samples display a large variation of lead concentrations, from 16 ppb for a harzburgite to up to 400 ppb for a lherzolite. However, their lead isotope ratios are relatively homogeneous with 206Pb /204Pb of 19.07 ± 0.08, 207Pb /204Pb of 15.65 ± 0.07, and 208Pb /204Pb of 38.67 ± 0.17 ( n = 7). However, the 238U /204Pb ratios display a large variation, from 12.2 to 46.5, and do not correlate with indices of fertility such as calcium or aluminum content. Mineral separates yield even larger variations in lead isotopic composition and lead and uranium concentrations. Some olivine fractions have both the lowest radiogenic compositions ( 206Pb /204Pb = 18.75 ) and the lowest 238U /204Pb ratios (˜3.1). Clinopyroxenes (cpx) display the highest lead and uranium concentrations (up to 1277 ppb and 195 ppb, respectivelly) and generally similar or more radiogenic lead isotopic composition and higher 238U /204Pb ratios than their whole-rock compositions. Orthopyroxene and spinel fractions yield intermediate compositions between olivine and cpx. Although whole rocks and cpx for individual samples yield almost identical 87Sr /86Sr , the xenoliths ( n = 5) display a large variation of strontium isotopic compositions ( 87Sr /86Sr from 0.07033 to 0.7050), lead and strontium isotope ratios of cpx and the distribution of the data in a UPb isochron diagram suggest that the subcontinental lithosphere under the Yukon was affected by a recent (< ˜30 Ma) enrichment in uranium, lead, and strontium. The metasomatic fluid/magma might have had an isotopic composition close to that of some sediments in the northern Pacific Ocean. When compared to K d values reported in the literature, olivine is enriched in

  4. Source of lead in Central American and Caribbean mineralization, II. Lead isotope provinces

    NASA Astrophysics Data System (ADS)

    Cumming, George L.; Kesler, Stephen E.; Krstic, Dragan

    1981-12-01

    In an earlier study of Mesozoic and Cenozoic mineralization in Central America and the Caribbean region, we found that lead isotopic compositions of deposits in northern Central America, which is underlain by a pre-Mesozoic craton, ranged to higher 206Pb/ 204Pb and 207Pb/ 204Pb compositions than did deposits from elsewhere in the region, where the basement is Mesozoic oceanic material. Using 16 analyses for 12 new deposits, as well as new analyses for 11 of the samples studied previously, we have found that lead isotopic compositions correlate closely with crustal type but show little or no correlation with depth to the M-discontinuity. The deposits are divisible into three main groups including (in order of increasing 207Pb/ 204Pb and 208Pb/ 204Pb ratio): (1) deposits in southern Central America and all deposits in the Greater Antilles except Cuba; (2) all deposits in northern Central America; and (3) the Cuban deposits. Southern Central American and Caribbean lead is higher in 207Pb/ 204Pb and 208Pb/ 204Pb than most mid-ocean ridge basalts but could have been derived directly or indirectly from undepleted mantle. Northern Central America can be divided into the Maya block, which belongs to the Americas plate, and the Chortis block, which belongs to the Caribbean plate. Maya block deposits fall along a linear array whereas those of the Chortis block (except the Monte Cristo deposit) form a cluster. These results suggest that the Maya block is underlain by crust or mantle with a large range of U/Pb and Th/U ratios, whereas the Chortis block basement is more homogeneous. Two-stage model calculations indicate an age of about 2280±310 m.y. for the Maya block basement, although no such rocks are known in the region. Comparison of the Chortis block data to our recently published lead isotopic analyses of Mexican deposits shows considerable similarities suggesting that the Chortis block could have been derived from Mexico.

  5. A Geochemical and Isotopic Study of the Youngest Lavas from the Islands of Upolu and Savai’i, Samoa

    NASA Astrophysics Data System (ADS)

    Buhler, A.; Pietruszka, A. J.; Hanan, B. B.

    2009-12-01

    We report major and trace element abundances and Hf, Pb, Sr, and Nd isotopic ratios for eight of the youngest rejuvenation stage lavas from the Samoan Islands of Upolu and Savai’i. The extensive and voluminous amount of rejuvenation stage volcanism on the Samoan islands, especially on the islands of Savai’i and Upolu, has made these islands key in the understanding of rejuvenation magmatism. The six lavas from Upolu are basanites, whereas the two lavas from Savai’i are alkali basalts. With the exception of one basanite with 7.4 wt. % MgO, all of the samples are relatively primitive (MgO = 10.5 to 12.2 wt. %) and show little evidence of fractionation beyond olivine control. However, variations in major element abundances at a given MgO value indicate changes in the parental melt composition. This interpretation is confirmed by wide variations in ratios of incompatible trace elements (e.g., Nb/La or Ce/Yb). On a primitive mantle normalized trace element diagram, the lavas have relatively constant, low abundances of heavy rare-earth elements (e.g., Yb) due to the presence of residual garnet in the mantle source region. The ɛNd (-0.3 to +2.9) and ɛHf (+3.7 to +8.0) values, and Pb isotope ratios (e.g., 206Pb/204Pb = 18.57-18.88, Δ207Pb/204Pb = 3.3-11.4, and Δ208Pb/204Pb = 59.4-76.3) vary significantly but plot within the range of published data for rejuvenation stage lavas from these islands. On a plot of ɛNd vs. 206Pb/204Pb, the new Upolu and Savai’i analyses make a distinctive positive correlation that overlaps with previous analyses of rejuvenation stage lavas from these islands. Interestingly, this trend is distinct from the ones defined by many of the purported Upolu and Savai’i shield stage lavas. These data will help to better understand the origin of rejuvenation stage magmatism.

  6. CONCH: A Visual Basic program for interactive processing of ion-microprobe analytical data

    NASA Astrophysics Data System (ADS)

    Nelson, David R.

    2006-11-01

    A Visual Basic program for flexible, interactive processing of ion-microprobe data acquired for quantitative trace element, 26Al- 26Mg, 53Mn- 53Cr, 60Fe- 60Ni and U-Th-Pb geochronology applications is described. Default but editable run-tables enable software identification of secondary ion species analyzed and for characterization of the standard used. Counts obtained for each species may be displayed in plots against analysis time and edited interactively. Count outliers can be automatically identified via a set of editable count-rejection criteria and displayed for assessment. Standard analyses are distinguished from Unknowns by matching of the analysis label with a string specified in the Set-up dialog, and processed separately. A generalized routine writes background-corrected count rates, ratios and uncertainties, plus weighted means and uncertainties for Standards and Unknowns, to a spreadsheet that may be saved as a text-delimited file. Specialized routines process trace-element concentration, 26Al- 26Mg, 53Mn- 53Cr, 60Fe- 60Ni, and Th-U disequilibrium analysis types, and U-Th-Pb isotopic data obtained for zircon, titanite, perovskite, monazite, xenotime and baddeleyite. Correction to measured Pb-isotopic, Pb/U and Pb/Th ratios for the presence of common Pb may be made using measured 204Pb counts, or the 207Pb or 208Pb counts following subtraction from these of the radiogenic component. Common-Pb corrections may be made automatically, using a (user-specified) common-Pb isotopic composition appropriate for that on the sample surface, or for that incorporated within the mineral at the time of its crystallization, depending on whether the 204Pb count rate determined for the Unknown is substantially higher than the average 204Pb count rate for all session standards. Pb/U inter-element fractionation corrections are determined using an interactive log e-log e plot of common-Pb corrected 206Pb/ 238U ratios against any nominated fractionation-sensitive species pair

  7. Fluid-rock interaction during progressive migration of carbonatitic fluids, derived from small-scale trace element and Sr, Pb isotope distribution in hydrothermal fluorite

    NASA Astrophysics Data System (ADS)

    Bühn, B.; Schneider, J.; Dulski, P.; Rankin, A. H.

    2003-12-01

    Associated with the Cretaceous Okorusu carbonatite complex (Namibia) is a hydrothermal fluorite mineralization hosted in Pan-African country rock marbles, which resulted from fluid-rock reaction between the marbles and orthomagmatic, carbonatitic fluids expelled from the carbonatite. Yellow fluorite I was deposited in veins up to 5 cm away from the wallrock contact, followed by purple and colorless fluorite II, smoky quartz and barite, a Mn-rich crust on early calcite, and pure calcite. This clear-cut sequence of mineral growth allows an investigation into fluid-rock interaction processes between the marble and the migrating carbonatitic fluid, and element fractionation patterns between the fluid and subsequent hydrothermal precipitates. Fluorite I shows a progressive change in color from dark yellow to colorless with purple laminations over time of deposition. Subsequent fluorite I precipitates show an increase in Ca, and a continuous decrease in F, Sr, REE, Y, Th, U and Pb contents. The ratios (Eu/Eu*) cn, Th/Pb and U/Pb increase whereas Y/Ho, Th/U and (La/Yb) cn decrease. The Sr-isotopic composition remains constant at 87Sr/ 86Sr = 0.70456-0.70459, but with varying, highly radiogenic Pb ( 206Pb/ 204Pb = 32-190, 238U/ 204Pb = 7-63). Fluorite II has 87Sr/ 86Sr = 0.70454-0.70459, 206Pb/ 204Pb = 18.349, and 207Pb/ 204Pb = 15.600, and a chemical composition similar to youngest fluorite I. The Mn-rich crust on early calcite accumulated REE, Ba, Pb, Zr, Cs, Th and U, developing into pure calcite with a prominent negative Ce anomaly and successively more radiogenic Sr. The calculated degrees of fluid-rock interaction, f = weight fraction of fluid/(fluid + marble), decrease from fluorite I and most fluorite II (f = 0.5) to calcite (f = 0.2-0.3) and hydrothermal quartz (f ≪ 0.1). A crush-leach experiment for fluid inclusions in the hydrothermal quartz yielded a Rb-Sr isochron age of 103 ± 12 Ma. Crush-leach analysis for the carbonatitic fluid trapped in the wallrock

  8. Childhood lead exposure in an industrial town in China: coupling stable isotope ratios with bioaccessible lead.

    PubMed

    Li, Hong-Bo; Chen, Kai; Juhasz, Albert L; Huang, Lei; Ma, Lena Q

    2015-04-21

    Fingerprinting based on stable isotopes of lead (Pb) in blood and environmental media helps to identify Pb exposure pathways in children. However, previous studies used stable isotopes of total Pb in media. In this study, a wire rope production town in China (Zhuhang) was selected for investigating the effectiveness of using isotope ratios in bioaccessible Pb to identify childhood Pb exposure pathways. Blood Pb levels of 115 children in Zhuhang were 1.7-20.4 μg dL(-1), averaging 6.1 ± 3.2 μg dL(-1) (mean ± standard deviation), and were ∼1.6 times the national average in China (3.9 ± 1.8 μg dL(-1)). Among different environmental media (housedust, soil, PM10, vegetables, rice, and drinking water), housedust (695 ± 495 mg kg(-1)) and vegetables [0.36 ± 0.40 mg (kg of fresh weight)(-1)] contained elevated Pb concentrations. The isotope ratios ((207)Pb/(206)Pb and (208)Pb/(206)Pb) of total Pb were the highest in housedust (0.8587 ± 0.0039 and 2.1049 ± 0.0087) but lower than blood Pb ratios (0.8634 ± 0.0027 and 2.1244 ± 0.0061). When using bioaccessible Pb in housedust (0.8639 ± 0.0018 and 2.1171 ± 0.0036), the isotope ratios overlapped with blood Pb ratios, suggesting that incidental ingestion of housedust was the predominant contributor to children's blood Pb. Coupling the stable isotope technique with bioaccessible Pb is more reliable for identifying Pb exposure pathways than total Pb determinations.

  9. Childhood lead exposure in an industrial town in China: coupling stable isotope ratios with bioaccessible lead.

    PubMed

    Li, Hong-Bo; Chen, Kai; Juhasz, Albert L; Huang, Lei; Ma, Lena Q

    2015-04-21

    Fingerprinting based on stable isotopes of lead (Pb) in blood and environmental media helps to identify Pb exposure pathways in children. However, previous studies used stable isotopes of total Pb in media. In this study, a wire rope production town in China (Zhuhang) was selected for investigating the effectiveness of using isotope ratios in bioaccessible Pb to identify childhood Pb exposure pathways. Blood Pb levels of 115 children in Zhuhang were 1.7-20.4 μg dL(-1), averaging 6.1 ± 3.2 μg dL(-1) (mean ± standard deviation), and were ∼1.6 times the national average in China (3.9 ± 1.8 μg dL(-1)). Among different environmental media (housedust, soil, PM10, vegetables, rice, and drinking water), housedust (695 ± 495 mg kg(-1)) and vegetables [0.36 ± 0.40 mg (kg of fresh weight)(-1)] contained elevated Pb concentrations. The isotope ratios ((207)Pb/(206)Pb and (208)Pb/(206)Pb) of total Pb were the highest in housedust (0.8587 ± 0.0039 and 2.1049 ± 0.0087) but lower than blood Pb ratios (0.8634 ± 0.0027 and 2.1244 ± 0.0061). When using bioaccessible Pb in housedust (0.8639 ± 0.0018 and 2.1171 ± 0.0036), the isotope ratios overlapped with blood Pb ratios, suggesting that incidental ingestion of housedust was the predominant contributor to children's blood Pb. Coupling the stable isotope technique with bioaccessible Pb is more reliable for identifying Pb exposure pathways than total Pb determinations. PMID:25803404

  10. Eruption of Alkaline Basalts Prior to the Calc-alkaline Lavas of Mt. Cleveland Volcano, Aleutian Arc, Alaska

    NASA Astrophysics Data System (ADS)

    Bridges, D. L.; Nicolaysen, K. P.

    2005-12-01

    Mt. Cleveland is a 1,730 m stratovolcano, located on Chuginadak Island, that has erupted at least 23 times historically, with the latest occurring in August 2005. Major, trace, and REE analyses of 63 samples from Mt. Cleveland, including 8 from proximal cinder cones and 4 from andesitic domes on the lower flanks, identify two distinct lava suites. Modern Cleveland (MC) basalts to dacites (50.5-66.7 wt.% SiO2) exhibit a calc-alkaline differentiation trend. Major element trends suggest crystal fractionation of plagioclase +/- ortho- and clinopyroxene in MC lavas and olivine in cinder cone deposits. Resorption textures on plagioclase and olivine phenocrysts and multiple populations of plagioclase predominate throughout the MC suite suggesting magma mixing is a major process at Cleveland. Frothy white xenoliths of plagioclase + quartz + biotite are encased in glass and erupted as small pumiceous fragments in 2001. The partial resorption of the xenocrysts indicates assimilation is also an active crustal process at Cleveland. MC trace element spider diagrams exhibit a typical arc pattern in which HFS elements including Nb are depleted, and Pb and LIL elements are enriched. Th/La, Sm/La, and Sr, Nd, Pb, and Hf isotopic ratios indicate both a North Pacific MORB and a sediment component in the source of modern Cleveland lavas, consistent with sediment flux estimates of 90 to 95 m3/m/yr and an updip sediment thickness of 1300 to 1400 meters. Average 206Pb/204Pb, 207Pb/204Pb, 87Sr/86Sr, and 143Nd/144Nd values for the calc-alkaline suite are 18.93, 15.58, 0.70345, and 0.51303 respectively. The second suite consists of 3 olivine-rich, mildly alkaline basalts (48.5-49.4 wt.% SiO2), of older stratigraphic position than MC lavas representing deposits from an older phase of activity (ancestral Cleveland, AC). La/Yb, Sr/Y, and Th/Nb ratios indicate lower degrees of partial melting, relative to MC lavas, and suggests presence of garnet in the source region. The AC lavas, however, are

  11. Nd, Sr, Pb, Ar, and O isotopic systematics of Sturgeon Lake kimberlite, Saskatchewan, Canada: constraints on emplacement age, alteration, and source composition

    NASA Astrophysics Data System (ADS)

    Hegner, E.; Roddick, J. C.; Fortier, S. M.; Hulbert, L.

    1995-06-01

    Rb-Sr isotopic dating of phlogopite megacryst samples separated from Sturgeon Lake kimberlite, Saskatchewan, yields a crystallization age of 98±1 Ma (2 σ, MSWD=1.2; 87Sr/86Sr( t)=0.7059). The 40Ar/39Ar analyses of a phlogopite megacryst sample indicate the presence of large amounts of excess 40Ar and yield an excessively old age of ˜410 Ma. Assessment of the Ar data using isotope correlation plots indicates clustering of the data points about a mixing line between the radiogenic 40Ar component at 98 Ma and a trapped component with uniform 36Ar/40Ar and Cl/40Ar. Values of δ 18O as high as +20‰ (VSMOW) for calcite from the groundmass and a whole-rock sample indicate pervasive low-temperature alteration. The δ 13C of matrix carbonate is -11.3‰ (PDB), slightly lighter than typical values from the literature. The δ 18O values of about +5‰ (VSMOW) for brown phlogopite megacrysts may be primary, green phlogopites are interpreted to be an alteration product of the brown variety and are 2‰ heavier. Initial Nd-Sr-Pb isotopic ratios for a whole-rock sample ( ɛ Nd=+0.8; 87Sr/86Sr=0.7063, 206Pb/204Pb=18.67, 207Pb/204Pb=15.54, 208Pb/204Pb=38.97) suggest an affinity with group I kimberlites. Initial ɛ Nd values of +1.7 and +0.5 (87Sr/86Sr( t)=0.7053 and 0.7050) for eclogitic and lherzolitic garnet megacryst samples, and values of 0.0 for two phlogopite megacryst samples reflect an origin from an isotopically evolving melt due to assimilation of heterogeneous mantle. Lilac high-Cr lherzolitic garnet megacrysts give an unusually high ɛ Nd(98. Ma) of +28.6 (87Sr/86Sr=0.7046) indicating a xenocrystic origin probably from the lithospheric mantle. The very radiogenic 87Sr/86Sr and 206Pb/204Pb ratios of the kimberlite are consistent with melting of EM II (enriched) mantle components.

  12. Effects of interaction between ultramafic tectonite and mafic magma on Nd-Pb-Sr isotopic systems in the Neoproterozoic Chaya Massif, Baikal-Muya ophiolite belt

    USGS Publications Warehouse

    Amelin, Y.V.; Ritsk, E. Yu; Neymark, L.A.

    1997-01-01

    Sm-Nd, Rb-Sr and U-Pb isotopic systems have been studied in minerals and whole rocks of harzburgites and mafic cumulates from the Chaya Massif, Baikal-Muya ophiolite belt, eastern Siberia, in order to determine the relationship between mantle ultramafic and crustal mafic sections. Geological relations in the Chaya Massif indicate that the mafic magmas were emplaced into, and interacted with older solid peridotite. Hand picked, acid-leached, primary rock-forming and accessory minerals (olivine, orthopyroxene, clinopyroxene and plagioclase) from the two harzburgite samples show coherent behavior and yield 147Sm/144Nd- 143Nd/144Nd and 238U/204Pb-206Pb/204Pb mineral isochrons, corresponding to ages of 640 ?? 58 Ma (95% confidence level) and 620 ?? 71 Ma, respectively. These values are indistinguishable from the crystallization age of the Chaya mafic units of 627 ?? 25 Ma (a weighted average of internal isochron Sm-Nd ages of four mafic cumulates). The Rb-Sr and Sm-Nd isotopic systems in the harzburgite whole-rock samples were disturbed by hydrothermal alteration. These alteration-related isotopic shifts mimic the trend of variations in primary isotopic compositions in the mafic sequence, thus emphasizing that isotopic data for ultramafic rocks should be interpreted with great caution. On the basis of initial Sr and Nd values, ultramafic and mafic rocks of the Chaya Massif can be divided into two groups: (1) harzburgites and the lower mafic unit gabbronorites with ??Nd = +6.6 to +7.1 and ??Sr = -11 to -16; and (2) websterite of the lower unit and gabbronorites of the upper mafic unit: ??Nd = + 4.6 to + 6.1 and ??Sr = - 8 to -9. Initial Pb isotopic ratios are identical in all rocks studied, with mean values of 206Pb/204Pb = 16.994 ?? 0.023 and 207Pb/204Pb = 15.363 ?? 0.015. The similarity of ages and initial isotopic ratios within the first group indicates that the isotopic systems in the pre-existing depleted peridotite were reset by extensive interaction with basaltic

  13. H, O, Sr, Nd, and Pb isotope geochemistry of the Latir volcanic field and cogenetic intrusions, New Mexico, and relations between evolution of a continental magmatic center and modifications of the lithosphere

    USGS Publications Warehouse

    Johnson, C.M.; Lipman, P.W.; Czamanske, G.K.

    1990-01-01

    Over 200 H, O, Sr, Nd, and Pb isotope analyses, in addition to geologic and petrologic constraints, document the magmatic evolution of the 28.5-19 Ma Latir volcanic field and associated intrusive rocks, which includes multiple stages of crustal assimilation, magma mixing, protracted crystallization, and open- and closed-system evolution in the upper crust. In contrast to data from younger volcanic centers in northern New Mexico, relatively low and restricted primary ??18O values (+6.4 to +7.4) rule out assimilation of supracrustal rocks enriched in 18O. Initial 87Sr/86Sr ratios (0.705 to 0.708), ??18O values (-2 to-7), and 206Pb/204Pb ratios (17.5 to 18.4) of metaluminous precaldera volcanic rocks and postcaldera plutonic rocks suggest that most Latir rocks were generated by fractional crystallization of substantial volumes of mantle-derived basaltic magma that had near-chondritic Nd isotope ratios, accompanied by assimilation of crustal material in two main stages: 1) assimilation of non-radiogenic lower crust, followed by 2) assimilation of middle and upper crust by inter-mediate-composition magmas that had been contaminated during the first stage. Magmatic evolution in the upper crust peaked with eruption of the peralkaline Amalia Tuff (???26 Ma), which evolved from metaluminous parental magmas. A third stage of late, roofward assimilation of Proterozoic rocks in the Amalia Tuff magma is indicated by trends in initial 87Sr/86Sr and 206Pb/204Pb ratios from 0.7057 to 0.7098 and 19.5 to 18.8, respectively, toward the top of the pre-eruptive magma chamber. Highly evolved postcaldera plutons are generally fine grained and are zoned in initial 87Sr/86Sr and 206Pb/204Pb ratios, varying from 0.705 to 0.709 and 17.8 to 18.6, respectively. In contrast, the coarser-grained Cabresto Lake (???25 Ma) and Rio Hondo (???21 Ma) plutons have relatively homogeneous initial 87Sr/86Sr and 206Pb/204Pb ratios of approximately 0.7053 and 17.94 and 17.55, respectively. ??18O values for

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

    USGS Publications Warehouse

    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

  15. Oceanic Pb-isotopic sources of proterozoic and paleozoic volcanogenic massive sulfide deposits on Prince of Wales Island and vicinity, southeastern Alaska

    USGS Publications Warehouse

    Ayuso, Robert A.; Karl, Susan M.; Slack, John F.; Haeussler, Peter J.; Bittenbender, Peter E.; Wandless, Gregory A.; Colvin, Anna

    2005-01-01

    Volcanogenic massive sulfide (VMS) deposits on Prince of Wales Island and vicinity in southeastern Alaska are associated with Late Proterozoic through Cambrian volcanosedimentary rocks of the Wales Group and with Ordovician through Early Silurian felsic volcanic rocks of the Moira Sound unit (new informal name). The massive sulfide deposits in the Wales Group include the Big Harbor, Copper City, Corbin, Keete Inlet, Khayyam, Ruby Tuesday, and Stumble-On deposits, and those in the Moira Sound unit include the Barrier Islands, Moira Copper, Niblack, and Nichols Bay deposits. Pb-isotopic signatures were determined on sulfide minerals (galena, pyrite, chalcopyrite, pyrrhotite, and sphalerite) to constrain metal sources of the massive sulfides and for comparison with data for other deposits in the region. Except for the Ruby Tuesday deposit, galena is relatively rare in most of these deposits. Pb-isotopic signatures distinguish the mainly Cu+Zn±Ag±Au massive sulfide deposits in the Wales Group from the Zn+Cu±Ag±Au massive sulfide deposits in the Moira Sound unit. Among the older group of deposits, the Khayyam deposit has the widest variation in Pb-isotopic ratios (206Pb/204Pb=17.169–18.021, 207Pb/204Pb=15.341–15.499, 208Pb/204Pb=36.546–37.817); data for the other massive sulfide deposits in the Wales Group overlap the isotopic variations in the Khayyam deposit. Pb-isotopic ratios for both groups of deposits are lower than those on the average crustal Pbevolution curve (µ=9.74), attesting to a large mantle influence in the Pb source. All the deposits show no evidence for Pb evolution primarily in the upper or lower continental crust. Samples from the younger group of deposits have scattered Pb-isotopic compositions and plot as a broad band on uranogenic and thorogenic Pb diagrams. Data for these deposits overlap the trend for massive sulfide deposits in the Wales Group but extend to significantly more radiogenic Pb-isotopic values. Pb-isotopic ratios of

  16. Early Archean crustal evolution of the Jack Hills Zircon source terrane inferred from Lu-Hf, 207Pb/ 206Pb, and δ 18O systematics of Jack Hills zircons

    NASA Astrophysics Data System (ADS)

    Bell, Elizabeth A.; Harrison, T. Mark; McCulloch, Malcolm T.; Young, Edward D.

    2011-09-01

    Several lines of isotopic evidence - the most direct of which is from Hadean Jack Hills zircons - suggest a very early history of crust formation on Earth that began by about 4.5 Ga. To constrain both the fate of the reservoir for this crust and the nature of crustal evolution in the sediment source region of the Jack Hills, Western Australia, during the early Archean, we report here initial 176Hf/ 177Hf ratios and δ 18O systematics for <4 Ga Jack Hills zircons. In contrast to the significant number of Hadean zircons which contain highly unradiogenic 176Hf/ 177Hf requiring a near-zero Lu/Hf reservoir to have separated from the Earth's mantle by 4.5 Ga, Jack Hills zircons younger than ca. 3.6 Ga are more radiogenic than -13ɛ (CHUR) at 3.4 Ga in contrast to projected values at 3.4 Ga of -20ɛ for the unradiogenic Hadean reservoir indicating that some later juvenile addition to the crust is required to explain the more radiogenic younger zircons. The shift in the Lu-Hf systematics together with a narrow range of mostly mantle-like δ 18O values among the <3.6 Ga zircons (in contrast to the spread towards sedimentary δ 18O among Hadean samples) suggests a period of transition between 3.6 and 4 Ga in which the magmatic setting of zircon formation changed and the highly unradiogenic low Lu/Hf Hadean crust ceased to be available for intracrustal reworking. Constraining the nature of this transition provides important insights into the processes of crustal reworking and recycling of the Earth's Hadean crust as well as early Archean crustal evolution.

  17. A radiogenic isotopic (He-Sr-Nd-Pb-Os) study of lavas from the Pitcairn hotspot: Implications for the origin of EM-1 (enriched mantle 1)

    NASA Astrophysics Data System (ADS)

    Garapić, G.; Jackson, M. G.; Hauri, E. H.; Hart, S. R.; Farley, K. A.; Blusztajn, J. S.; Woodhead, J. D.

    2015-07-01

    We present new He-Sr-Nd-Pb-Os isotopic compositions and major and trace-element concentrations for ten subaerially-erupted lavas and one seamount lava associated with the Pitcairn hotspot. The most geochemically-enriched lavas at the Pitcairn hotspot have signatures that are consistent with recycled sediments derived from upper continental crust. Pitcairn lavas have elevated Ti, which also supports the presence of a mafic protolith in the Pitcairn mantle. A subset of Pitcairn seamount samples, including the seamount sample presented here, are tholeiitic. Tholeiitic lavas are uncommon at ocean hotspots located far from mid-ocean ridges. Like tholeiites that erupted in Hawaii, the presence of tholeiites in the Pitcairn magmatic suite can be explained by melting a silica-saturated recycled mafic component in the Pitcairn mantle source. We also present the highest 3He/4He ratio (12.6 Ra, ratio to atmosphere) from the Pitcairn hotspot. This sample anchors the high 206Pb/204Pb portion of the Pitcairn array and provides evidence for a plume component in the Pitcairn mantle. In contrast, Pitcairn lavas that have the lowest 206Pb/204Pb are the most geochemically enriched, and have the highest 87Sr/86Sr and lowest 143Nd/144Nd in the Pitcairn suite; these EM-1 end-member lavas have MORB-like 3He/4He (~ 8 Ra, ratio to atmosphere). Recycled oceanic crust and sediment suggested to be in the Pitcairn EM-1 mantle are expected to have low 3He/4He (< 0.1 Ra). Therefore, the higher, MORB-like 3He/4He in Pitcairn EM-1 lavas is paradoxical, but might be explained by diffusive exchange of helium, but not the heavy radiogenic isotopes, with the ambient mantle over billion-year timescales.

  18. Identification of secondary lead sources in the air of an urban environment

    NASA Astrophysics Data System (ADS)

    Chiaradia, Massimo; Gulson, Brian L.; James, Matthew; William Jameson, C.; Johnson, David

    High precision lead isotopic data have been measured from particulates deposited on filters from two suburbs of Sydney (NSW, Australia) and gasoline from two main brands to evaluate the source of lead in air following the phasing out of leaded gasoline in Sydney in 1986 and a 25% reduction of lead in leaded gasoline in 1994. These measures have resulted in a 75% reduction of lead in Sydney air nowadays. Despite these positive figures, our results indicate that gasoline still accounts for more than 90% of the lead in the atmosphere of this city. However, when compared with an earlier investigation carried out in the period 1979-1981, our data show that a background source with a 206Pb/ 204Ph isotopic ratio higher than petrol has become detectable. We have used a best fitting mathematical procedure to identify the isotopic ratio and percentage contribution of this source to the air. The values that we have obtained are ˜ 18.2 and ˜7%, respectively, for the 206Pb/204Pb ratio and the percentage contribution. Several local background sources are considered, including natural lead from soils, wood burning, coal burning in power stations and aircraft profellants. We also draw attention to the similarity of the background isotopic composition in Sydney air aid isotopic ratios measured in snows of Antarctica.

  19. Bone lead levels and lead isotope ratios in red grouse from Scottish and Yorkshire moors.

    PubMed

    Thomas, Vernon G; Scheuhammer, Anton M; Bond, Della E

    2009-05-15

    Leg and foot bones of adult and juvenile red grouse (Lagopus lagopus scoticus) were collected from hunter-shot birds on two Scottish estates (Glendye and Invermark) and one Yorkshire estate in September, 2003. The lead content of bones was measured by atomic absorption spectrophotometry, and corresponding stable lead isotopes (Pb(204, 206, 207, 208)) by inductively coupled plasma mass spectrometry. At the Glendye (N=111) and Invermark (N=85) estates, relatively few birds (5.4% and 3.5%, respectively) had highly elevated bone lead concentrations (>20 microg/g dry weight). In bones of these highly exposed birds, a combination of Pb(206):Pb(207) and Pb(208):Pb(207)ratios was consistent with ingestion of lead gunshot available in Europe. By contrast, Yorkshire grouse experienced a high incidence (65.8%) of bone lead >20 microg/g. The Pb(206):Pb(207) and Pb(208):Pb(207)ratios in bones of these highly exposed birds were consistent with a combined exposure to ingested lead gunshot and lead from galena mining in the region. Lead isotope ratios also indicated that lead from UK gasoline combustion and fallout from atmospheric particles was not a likely source of elevated lead in bones of either Scottish or Yorkshire grouse. Suggested management options for the three moors include adopting nontoxic shot for all game shooting on the estates, allowing heather (Calluna vulgaris) vegetation to grow tall in lead shot fall-out zones to reduce physical access to high densities of lead shot already present, and provision of calcareous grit across moors to reduce lead assimilation from all ingested sources of lead.

  20. Mantle Heterogeneity and Mixing Beneath the Bouvet Triple Junction Region: Hf Isotope Constraints from the Westernmost Southwest Indian Ridge (0-11deg.E)

    NASA Astrophysics Data System (ADS)

    Janney, P. E.; le Roex, A. P.

    2013-12-01

    We have undertaken new Hf (and supplementary Sr, Nd and Pb) isotope and trace element measurements of MORB from the westernmost Southwest Indian Ridge (SWIR; 0 to 11 deg. E) in order to clarify mixing relationships and the effect of the Bouvet and other local hot spots on the composition of the upper mantle beneath the Bouvet Triple Junction (BTJ) region. The new data are fully consistent with the findings of previous studies (le Roex et al., J. Petrol., 1983; Kurz et al., GCA, 1998) that isotopic heterogeneity in this region is largely explained by mixing between a moderately depleted mantle source (i.e., ɛHf ≈ +14, ɛNd ≈ +9, 87Sr/86Sr ≈ 0.7026; 206Pb/204Pb ≈ 18.5) and an enriched component isotopically similar to Bouvet OIB. Unlike the pattern expressed by He isotopes (Kurz et al., GCA, 1998; Georgen et al., EPSL, 2003) the strength of the Bouvet hot spot signature in terms of Hf-Sr-Nd-Pb isotope ratios is not well correlated with distance from Bouvet Island along ridge, except in the most general sense. Some MORB from 0-11E do approach the Hf-Sr-Nd-Pb isotopic composition of Bouvet OIB. However, the most extreme isotopic compositions (with ɛHf values that are slightly lower than, and Nd and Pb isotope compositions that are equivalent to, those of Bouvet OIB), are actually found in MORB from the 11-16E oblique spreading segment of the SWIR (le Roex et al., CMP, 1992; Janney et al., J. Petrol., 2005), located further from Bouvet Island than the segments at 0-11E. The lack of a strong correlation between the radiogenic isotope ratios of SWIR MORB and proximity to the Bouvet hot spot in this region supports the notion that local conditions of melting of a lithologically heterogeneous mixture of enriched, Bouvet hot spot-derived and depleted mantle materials plays the dominant role in controlling the radiogenic isotope composition of western SWIR MORB (le Roex et al., CMP, 1992; Salters & Dick, Nature, 2002). The depleted mantle present beneath the western

  1. Age and Geochemical Data From the Madeira-Tore Rise and Surrounding Seamounts: New Insights Into East Atlantic Volcanism

    NASA Astrophysics Data System (ADS)

    Geldmacher, J.; Hoernle, K. A.; Kluegel, A.; van den Bogaard, P.

    2003-12-01

    Located off the NW African continental margin is a >3000 km long belt of volcanic archipelagoes (e.g. Canary, Madeira Islands) and large seamounts including the 900 km long Madeira-Tore Rise (MTR). The cause of the East Atlantic volcanism, and in particular the origin and age of the MTR, which is composed of a widespread plateau with several seamount groups, is controversial. Proposed models include an origin of the MTR at the Mid Atlantic Ridge, formation over a hotspot, or as a product of diffuse small-scale mantle convection. All recently dredged volcanic samples (RV Meteor cruise M51/1) from the MTR and nearby off-rise seamounts exhibit enriched Ocean Island Basalt-like incompatible trace element signatures similar to HIMU (high time integrated 238U/204Pb) ocean islands. Their isotope compositions are similar to those from Madeira with 87Sr/86Sr and 143Nd/144Nd overlapping Atlantic N-MORB to a large extent, but Pb isotope ratios plotting well below the Northern Hemisphere Reference Line and extending to 206Pb/204Pb values of 19.90. Our preliminary data confirm the existence of at least two distinct isotopic domains in the eastern North Atlantic: 1) a Madeira-like domain (as characterized above) stretching from Madeira Island along the MTR to the NE as far as the Azores Gibraltar fracture zone, and 2) a Canary-like domain with Sr, Nd, Pb isotope ratios intermediate between N-MORB and HIMU (206Pb/204Pb = 19.0-20.2; 207Pb/204Pb = 15.54-15.66) but with lower 143Nd/144Nd ratios (<0.5130) than the Madeira domain. We interpret the distinct compositions of these domains to reflect spatial zonation in the deeper sources of the mantle upwellings. The domains include zones influenced by Enriched Mantle (EM) I and II, which appear to be orientated along the extension of the Oceanographer (at ˜ 34° N) and the Azores-Gibraltar fracture zones (at ˜ 37° N), respectively. The first zone includes a hitherto unknown seamount that exhibits the most extreme EM I composition yet

  2. Comparison of the concentrations of metal elements and isotopes of lead found in rice and rice bran.

    PubMed

    Dai, Shouhui; Yang, Hui; Yang, Lan; Wang, Fuhua; Du, Ruiying; Wen, Dian

    2014-08-01

    Very few studies have investigated the difference in the distribution of metal elements between rice and rice bran samples. In this study, the concentrations of 27 metal elements (Li, Be, Na, Mg, Al, K, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Ag, Cd, Cs, Ba, Tl, Pb, and U) in 56 polished rice and their corresponding bran samples were determined. A significant difference in concentrations of all elements except Ag and Cd was found between rice and bran (P < 0.05), with bran/rice ratios of 1.21 to 36.3. High concentrations of metal elements, especially that of the heavy metal Cr, in bran samples present a potential safety issue for bran products, such as food and feed containing bran. Pb isotope ((204)Pb, (206)Pb, (207)Pb, and (208)Pb) ratios also were determined. The (206)Pb/(207)Pb and (208)Pb/(207)Pb ratios in bran were generally higher than those in rice (P < 0.0001), and rice and bran samples were distinctly different from each other, indicating that Pb isotope composition is an effective for discriminating between bran and rice samples.

  3. Comparison of the concentrations of metal elements and isotopes of lead found in rice and rice bran.

    PubMed

    Dai, Shouhui; Yang, Hui; Yang, Lan; Wang, Fuhua; Du, Ruiying; Wen, Dian

    2014-08-01

    Very few studies have investigated the difference in the distribution of metal elements between rice and rice bran samples. In this study, the concentrations of 27 metal elements (Li, Be, Na, Mg, Al, K, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Ag, Cd, Cs, Ba, Tl, Pb, and U) in 56 polished rice and their corresponding bran samples were determined. A significant difference in concentrations of all elements except Ag and Cd was found between rice and bran (P < 0.05), with bran/rice ratios of 1.21 to 36.3. High concentrations of metal elements, especially that of the heavy metal Cr, in bran samples present a potential safety issue for bran products, such as food and feed containing bran. Pb isotope ((204)Pb, (206)Pb, (207)Pb, and (208)Pb) ratios also were determined. The (206)Pb/(207)Pb and (208)Pb/(207)Pb ratios in bran were generally higher than those in rice (P < 0.0001), and rice and bran samples were distinctly different from each other, indicating that Pb isotope composition is an effective for discriminating between bran and rice samples. PMID:25198608

  4. "Canadian" Radiogenic Isotope Signature of Younger Dryas Age Sediments from the Central Arctic and Fram Strait Areas

    NASA Astrophysics Data System (ADS)

    Maccali, J.; Hillaire-Marcel, C.; Not, C.; Poirier, A.

    2011-12-01

    Recent work on sediment-core from the central Lomonosov Ridge (TWC- & MC-18) yielded evidence for active Ice-Rafted Deposition (IRD) during the Younger Dryas (YD), following a sedimentary hiatus spanning broadly the Last Glacial Maximum (LGM) [Hanslik et al., Quaternary Sci. Rev. 29: 3430-3441, 2010]. The YD interval is also recorded in a core raised from below outflowing Arctic sea-ice and water masses in the Fram Strait area (MC-16), thus raising the issue of the role of freshwater/sea-ice export from the Arctic in the YD-slowdown of the Atlantic Meridional Overturning Circulation (AMOC). We report here about mineralogical, geochemical and radiogenic isotope studies (Pb, Nd, Sr) of these YD-sediments in relation with potential sea-ice/sediment source areas in the Arctic Ocean. Three major isotopic sectors have variably contributed to IRD along the Trans-Polar Drift route towards Fram Strait since the LGM : i) Arctic Canada (206Pb/204Pb ≥ 18.854, epsilon-Nd ≤ -13.2, 87Sr/86Sr ≥ 0.721), ii) Northern Russia- (206Pb/204Pb ≤ 18.45, epsilon-Nd ≤ -10.3 and 87Sr/86Sr ≤ 0.715) and iii) Greenland- (YD; 206Pb/204Pb ≤ 18.65, epsilon-Nd ≤ -12.5 and 87Sr/86Sr ≤ 0.718). Whereas distinct mixing-trends are observed prior and after the YD in the Fram Strait area, the YD itself depicts at both sites a strong isotopic excursion towards the Canadian source with isotopic ratios of 18.84, -13.2 and 0.721 respectively for 206Pb/204Pb, epsilon-Nd and 87Sr/86Sr. Both sites also recorded a 5-fold higher IRD rates during the YD, in comparison with their respective mean Holocene rate. In MC-18, a 5-fold higher 230Th-excess also characterizes the YD unit which shows high carbonate contents, in its silt to sand fractions, with equal amounts of calcite and dolomite, also pointing to a major role of Canadian supplies. These features are interpreted as an indication for a strong freshwater pulse from northwestern Canada, enhancing sea-ice production in the Beaufort Sea, thus a

  5. Lead isotopes combined with a sequential extraction procedure for source apportionment in the dry deposition of Asian dust and non-Asian dust.

    PubMed

    Lee, Pyeong-Koo; Yu, Soonyoung

    2016-03-01

    Lead isotopic compositions were determined in leachates that were generated using sequential extractions of dry deposition samples of Asian dust (AD) and non-Asian dust (NAD) and Chinese desert soils, and used to apportion Pb sources. Results showed significant differences in (206)Pb/(207)Pb and (206)Pb/(204)Pb isotopic compositions in non-residual fractions between the dry deposition samples and the Chinese desert soils while (206)Pb/(207)Pb and (206)Pb/(204)Pb isotopic compositions in residual fraction of the dry deposition of AD and NAD were similar to the mean (206)Pb/(207)Pb and (206)Pb/(204)Pb in residual fraction of the Alashan Plateau soil. These results indicate that the geogenic materials of the dry deposition of AD and NAD were largely influenced by the Alashan Plateau soil, while the secondary sources of the dry deposition were different from those of the Chinese desert soils. In particular, the lead isotopic compositions in non-residual fractions of the dry deposition were homogenous, which implies that the non-residual four fractions (F1 to F4) shared the primary anthropogenic origin. (206)Pb/(207)Pb values and the predominant wind directions in the study area suggested that airborne particulates of heavily industrialized Chinese cities were one of the main Pb sources. Source apportionment calculations showed that the average proportion of anthropogenic Pb in the dry deposition of AD and NAD was 87% and 95% respectively in total Pb extraction, 92% and 97% in non-residual fractions, 15% and 49% in residual fraction. Approximately 81% and 80% of the anthropogenic Pb was contributed by coal combustion in China in the dry deposition of AD and NAD respectively while the remainder was derived from industrial Pb contamination. The research result proposes that sequential extractions with Pb isotope analysis are a useful tool for the discrimination of anthropogenic and geogenic origins in highly contaminated AD and NAD.

  6. Multiple tree-ring isotopes as environmental indicators of diffuse atmospheric pollution in a peri-urban area

    NASA Astrophysics Data System (ADS)

    Doucet, A.; Savard, M. M.; Bégin, C.; Ouarda, T. B.; Marion, J.

    2010-12-01

    The combined analyses of tree-ring δ13C, δ18O, δ15N, 206Pb/207Pb, 206Pb/204Pb and 206Pb/208Pb isotope ratios of three red spruce specimens from the Tantaré ecological reserve located 40 km northwest of Québec City (Canada) were studied with the aim of reconstructing environmental conditions and unravel past air-quality changes of the 1880-2007 period. To separate the tree-ring δ18O and δ13C patterns induced by natural conditions from those generated by anthropogenic perturbations, a linear regression was applied between the most explicative meteorological parameters and the isotopic series for the period of low pollution (1880 to 1909). The model equations were then applied to the most recent part of the series (1910-2007) to verify if climatic conditions have remained the main driver of the tree-ring isotopic variations. The good fit between the modeled and measured δ18O series for the entire studied period suggests that the assimilation of oxygen by red spruce trees is not significantly affected by pollution stress near Québec City. However, the deviation between the measured and modeled δ13C values for the 1944-2007 period indicates that diffuse pollution affected carbon assimilation by the investigated trees. To independently validate if atmospheric pollution could have generated the deviation between the measured and the estimated δ13C values, a linear regression was applied between the portion of the residual δ13C values and atmospheric pollution (Canadian fossil fuel proxy from 1958 to 2000). The nice fit between the modeled δ13C values from the combination of the two regression analyses based on climate and emission proxy strongly supports the hypothesis that there is a natural and an anthropogenic portion in the δ13C variations of the studied specimens. The short-term variations of the red spruce δ15N series are correlated with the instrumentally measured amounts of provincial N emissions for the 1990 to 2006 period (longest measurements

  7. Lead Isotope Measurement by Lead Double Spike and Thallium Spike Using MC-ICP-MS and TIMS - a Comparison Using Basaltic Samples

    NASA Astrophysics Data System (ADS)

    Taylor, R. N.; Ishizuka, O.

    2001-12-01

    Multi-collector ICP-MS has provided a new level of precision to lead isotope analysis using Thallium addition as an internal mass bias monitor. Further enhancement of precision has been achieved by the application of double lead spike to measurement procedures. In this study, we directly compare results using thallium addition and the new SBL74 double lead spike on both TIMS and MC-ICP-MS (Micromass IsoProbe). The comparisons are performed using standard Pb solutions and basaltic matrix-bearing solutions. Analyses of standards measured over 8 analytical sessions using the thallium spike method are reproducible to within 100 ppm for 206Pb/204Pb, 130 ppm for 207Pb/204Pb and 220 ppm (2sd) for 208Pb/204Pb. If the ratios for individual analytical sessions are normalised to the SRM981{day average}/SRM981true the increasing error with greater mass difference of the ratio is eliminated and all ratios are less than ±85 ppm. This implies that variability between the Tl and Pb mass bias factors on a day-to-day basis is the cause of increasing imprecision with mass difference. Double spike MC-ICP-MS is found to produce similar levels of precision to the Tl method for standards. However, the decreasing precision with increasing mass difference is greatly reduced, indicating that the correlation is due to Tl and Pb differences. With basaltic matrix samples with a single anion exchange separation, the effects of Tl-Pb differential mass bias are slightly exaggerated. We present the results from mixtures of SRM981 with Pb-free Fe measured using MC-ICP-MS using Tl and double spike mass bias correction, to replicate the basaltic matrix analyses.

  8. A proposed new approach and unified solution to old Pb paradoxes

    NASA Astrophysics Data System (ADS)

    Castillo, Paterno R.

    2016-05-01

    One of the most remarkable features of many and, perhaps, all oceanic basalts is that their Pb isotopic ratios (206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb) are too radiogenic to be coming from the undifferentiated mantle or bulk silicate Earth. This has created three major concerns in the behavior of U, Th and Pb in the Earth's mantle that have been termed the Pb paradoxes. These are the unexpectedly long time-integrated high U/Pb (1st paradox), long time-integrated low Th/U (2nd paradox) and constant Ce/Pb and Nb/U (3rd paradox) in the mantle sources of oceanic basalts. The origins of such unexpected ratios have been the object of intense studies that produced several highly significant, but generally individualized results during the last four decades. Detailed analysis of available data shows that the paradoxes are closely interrelated as they all pertain to the mantle and have many common characteristic features. Thus, the Pb paradoxes constitute a system of equations that must be solved all together as each solution must satisfy every equation in the system. For example, compositional data for the voluminous mid-ocean ridge basalts (MORB) show that the 1st and 2nd paradoxes exhibit a long time-integrated enrichment of U and the Th/U and Nb/Th ratios are also constant. A single solution to simultaneously explain the paradoxes in MORB is possible if recycled materials with variable enrichments in incompatible trace elements, particularly U and its daughter Pb* plus Nb, Ce, and Th are added to or mixed with the depleted upper mantle. Significantly, a similar binary mixing solution has been proposed for the Pb paradoxes in ocean island basalts.

  9. Petrogenesis and geodynamics of plagiogranites from Central Turkey (Ekecikdağ/Aksaray): new geochemical and isotopic data for generation in an arc basin system within the northern branch of Neotethys

    NASA Astrophysics Data System (ADS)

    Köksal, Serhat; Toksoy-Köksal, Fatma; Göncüoglu, M. Cemal

    2016-09-01

    In the Late Cretaceous, throughout the closure of the Neotethys Ocean, ophiolitic rocks from the İzmir-Ankara-Erzincan ocean branch were overthrusted the northern margin of the Tauride-Anatolide Platform. The ophiolitic rocks in the Ekecikdaǧ (Aksaray/Central Turkey) region typify the oceanic crust of the İzmir-Ankara-Erzincan branch of Neotethys. The gabbros in the area are cut by copious plagiogranite dykes, and both rock units are intruded by mafic dykes. The plagiogranites are leucocratic, fine- to medium-grained calc-alkaline rocks characterized mainly by plagioclase and quartz, with minor amounts of biotite, hornblende and clinopyroxene, and accessory phases of zircon, titanite, apatite and opaque minerals. They are tonalite and trondhjemite in composition with high SiO2 (69.9-75.9 wt%) and exceptionally low K2O (<0.5 wt%) contents. The plagiogranites in common with gabbros and mafic dykes show high large-ion lithophile elements/high-field strength element ratios with depletion in Nb, Ti and light rare-earth elements with respect to N-MORB. The plagiogranites together with gabbros and mafic dykes show low initial 87Sr/86Sr ratios (0.70419-0.70647), high ƐNd(T) (6.0-7.5) values with 206Pb/204Pb (18.199-18.581), 207Pb/204Pb (15.571-15.639) and 208Pb/204Pb (38.292-38.605) ratios indicating a depleted mantle source modified with a subduction component. They show similar isotopic characteristics to the other supra-subduction zone (SSZ) ophiolites in the Eastern Mediterranean to East Anatolian-Lesser Caucasus and Iran regions. It is suggested that the Ekecikdaǧ plagiogranite was generated in a short time interval from a depleted mantle source in a SSZ/fore-arc basin setting, and its nature was further modified by a subduction component during intra-oceanic subduction.

  10. Mesozoic igneous intrusions in New England and Quebec: Implications from lead (Pb) isotopes on petrogenesis and mantle sources (Ascutney Mountain, Vermont; Mont Saint Hilaire, Quebec; Pliny Complex, New Hampshire)

    SciTech Connect

    Schucker, D.E.

    1992-01-01

    Lead isotopes are used to study Mesozoic intrusions from New England and Quebec, specifically the igneous complexes of Ascutney Mountain (Vermont), Mont Saint Hilaire (Quebec), and Pliny (New Hampshire). The main objectives are to address the: (1) petrogenesis of specific complexes using Pb isotopes along with previous results; and (2) sources of parental magmas in the context of a possible plume source for the Cretaceous intrusions and New England Seamounts. Analytical procedures for Pb and U are also described in detail. For each of the three complexes, significant variation in apparent initial [sup 208]Pb/[sup 204]Pb, [sup 207]Pb/[sup 204]Pb, and [sup 206]Pb/[sup 204]Pb ratios are observed. These variations reflect crustal contamination and local country rocks are isotopically suitable contaminants. Contamination lowers the Pb isotopic ratios of the modified magmas. The Pb ratios of the parental magmas are constrained by defining trends resulting from crustal contamination. At the Ascutney complex, granites appear to be uniform at the time of formation based on feldspar results. Granite whole rocks exhibit open system U-Pb behavior which is attributed to significant recent U loss (of up to 38%). Both local schists and gneisses are important contaminants with generally <25% contamination. Significant isotopic variations are apparent at Mont Saint Hilaire where rock-feldspar variations are apparently not in isotopic equilibrium. Feldspars reflect magmatic values and indicate crustal contamination of a parental magma for the Hilaire complex. A limited data set for the Pliny complex suggests a parental magma. The Pb results support a common mantle source for the Cretaceous continental intrusions (Ascutney and Mont Saint Hilaire) and the New England Seamounts. They imply magma from a sublithospheric mantle-plume, and that magmas ascended with little or no lithospheric interaction. The magma source for the Jurassic Pliny complex appears to be different.

  11. Alpha / Mendeleev Ridge and Chukchi Borderland 40Ar/39Ar Geochronology and Geochemistry: Character of the First Submarine Intraplate Lavas Recovered from the Arctic Ocean

    NASA Astrophysics Data System (ADS)

    Mukasa, Samuel B.; Mayer, Larry A.; Aviado, Kimberly; Bryce, Julie; Andronikov, Alex; Brumley, Kelley; Blichert-Toft, Janne; Petrov, Oleg; Shokalsky, Sergey

    2015-04-01

    At least three episodes of magmatic activity have been recognized on the basis of 40Ar/39Ar age determinations in the submarine basaltic samples dredged, drilled or grabbed with a manipulation arm from Alpha / Mendeleev Ridge and Chukchi Borderland of the Arctic Ocean by US Coast Guard Icebreaker Healy, in August-September 2008, and Russian research vessel Captain Dranitsin in August-October 2012: ca. 112 Ma, ca. 100 Ma and ca. 85-73 Ma. Major-oxide and trace-element concentrations, and Pb, Sr, Nd, and Hf isotopic ratios of the recovered lavas provide important constraints on the composition and sources for the original melts. Lavas erupted at ca. 112 Ma (Group 1) have alkali basalt major-oxide compositions. Their low degree of rare-earth-element (REE) fractionation (CeN/YbN = 1.7-2.5), combined with high overall HREE (22-24 times chondrite) and Mg# ~54, suggest derivation from a garnet-free source followed by only minimal crystal fractionation for this group. Pb-Sr-Nd-Hf isotopic systematics of the lavas (206Pb/204Pb = 18.73-18.79; 207Pb/204Pb = 15.54-15.56; 208Pb/204Pb = 38.28-38.35; 143Nd/144Nd = 0.512594-0.512610; 87Sr/86Sr = 0.709458-0.709601; 176Hf/177Hf = 0.283224), together with ratios of highly incompatible trace elements (Th/Ce = 0.09-0.11; Ce/Nb = 2.58-3.09; Th/Nb = 0.24-0.33), point toward a lithospheric source for the magmas. Eruptions at ca. 100 Ma and 85-73 Ma produced two types of lavas: low-Ti tholeiitic basalts - LT, and high-Ti alkali basalts - HT, both assigned to Group 2. This distribution of low- and high-Ti lavas is common in continental flood basalt (CFB) provinces elsewhere, and has been attributed to plume activity in some studies. The trace-element abundance patterns for these Group 2 Arctic lavas are also very similar to those of CFBs elsewhere. Their low degrees of REE fractionation (CeN/YbN = 2.0-3.3) accompanied by progressively decreasing Mg#s (from 53 to 33) suggest a garnet-free source, with the derivative magmas experiencing

  12. Pb-Sr-Nd isotope study of the 100- to 2700-Ma old alkalic rock-carbonatite complexes in the Canadian shield: inferences on the geochemical and structural evolution of the mantle

    SciTech Connect

    Kwon, S.T.

    1986-01-01

    The isotopic signatures of young continental alkalic complexes (CAC) display a remarkable similarity to those of oceanic island basalts (OIB). A study of Sr isotopic evolution showed that the mantle, presumably similar to the source of OIB, beneath the shield appears to have been depleted in large ion lithophile elements (LILE) and to have remained as a closed system since ca. 3000 Ma ago. The present investigations apply Pb and Nd as well as Sr isotopic systems for those complexes to study the secular geochemical evolution of the mantle over the past 2700 million years, and address the question of the processes responsible for the geochemical heterogeneity of the mantle. The data suggest: (1) Like Sr, Pb and Nd isotopic data indicate LILE depleted sources for the southern Canadian shield CAC over at least the past 1900 Ma. (2) Sr, Nd and Pb are compatible with an age of ca. 3000 Ma for the depleted source. (3) In contrast to Sr, and probably Nd, the Pb isotopic data cannot be explained by a closed system model for the depleted mantle source. (4) Coherent fractionation patterns are observed in the mantle sources of CAC since at least 1900 Ma ago: higher U/Pb and Sm/Nd, and lower Th/U and Rb/Sr ratios versus lower U/Pb and Sm/Nd, and higher Th/U and Rb/Sr ratios, indicating OlB-like sources for CAC. (5) The inverse correlation between /sup 206/Pb//sup 204/Pb and /sup 87/Sr//sup 86/Sr initial ratios permit calculation of apparent mean earth Pb isotope ratios with time, which yield 8.35 for the present day /sup 238/U//sup 204/Pb ratio, and 17.82 for /sup 206/Pb//sup 204/Pb. (6) A model for the geochemical and structural evolution of the mantle is based on the diverging isotopic evolution of the midocean ridge basalts (MORB) and OlB sources.

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

    NASA Astrophysics Data System (ADS)

    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

  14. Anthropogenic Pb input into Bohai Bay, China: Evidence from stable Pb isotopic compositions in sediments

    NASA Astrophysics Data System (ADS)

    Hu, Ningjing; Huang, Peng

    2016-04-01

    Anthropogenic Pb input into Bohai Bay, China: Evidence from stable Pb isotopic compositions in sediments Hu Ning-jinga, Huang Pengb,, Liu Ji-huaa, a First Institute of Oceanography, State Oceanic Administration, Qingdao 266061, China b Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China To investigate the source of Pb within Bohai Bay, Pb concentrations and Pb isotopic compositions (204Pb, 206Pb, 207Pb, and 208Pb) of surface sediments in this area were determined. The Pb concentration in this bay varied widely from 6.9 to 39.2 μg/g (average: 21.8 ± 7.8 μg/g), and the Pb isotopic compositions ranged from 0.8338 to 0.8864 (average: 2.0997 ± 0.0180) for 208Pb/206Pb and from 2.0797 to 2.1531 (average: 0.8477 ± 0.0135) for 207Pb/206Pb, presenting in three distinct clusters. The Pb isotopic ratios of sediments from the northeastern (NE zone) and northwestern (NW zone) coastal areas were significantly influenced by anthropogenic sources such as coal combustion and automobile emission. In sediments from the central and southern Bohai Bay (C-S zone); however, Pb mainly originated from the Yellow River catchment, as a result of lithogenic sediment (from rock weathering) accumulation. The Pb isotopic ratios further indicate that, apart from riverine inputs, the neighboring large-scale ports and aerosols significantly contributed to the anthropogenic Pb contained in these sediments. Pb contamination in the Haihe and Luanhe river mouths as well as in the regions near ports is also suggested from anthropogenic enrichment factors. As cities and ports continue to develop around Bohai Bay, a long-term extensive sewage monitoring program is highly recommended.

  15. Lead (Pb) fluxes and Pb isotopic compositions from Masaya Volcano, Nicaragua

    NASA Astrophysics Data System (ADS)

    Vallelonga, P.; Mather, T. A.

    We report Pb concentrations and isotopic compositions measured in plume aerosol and Pele's hair (lava) samples collected from Masaya volcano, Nicaragua, to provide the first data pertaining to Pb emissions from the Central American volcanic arc. Lead isotopic compositions, determined by Thermal Ionisation Mass Spectrometry, in the Pele's hair samples were found to be 206Pb/ 207Pb˜1.196, 208Pb/ 207Pb˜2.46 and 206Pb/ 204Pb˜18.6. Mean Pb fluxes from Masaya were calculated to be 1.0 ton Pb yr -1 with a mean plume Pb/S (gas) ratio of 1.3×10 -5. Also, it was found that the majority of Pb emitted was present in the fine aerosol (<2.5 μm diameter) fraction but that the percentage of Pb in the fine aerosol fraction decreased from 96% in the dry daytime plume to 61% in the condensed night-time plume. The contribution from the filter blank was usually a substantial fraction of the total amount of Pb measured, requiring the data to be corrected for blank contributions using Pb isotopic systematics.

  16. Pb, Sr, and Nd isotopes in basalts and sulfides from the Juan de Fuca Ridge

    SciTech Connect

    Hegner, E.; Tatsumoto, M.

    1987-10-10

    Pb, Sr, Nd isotopes of seven basalt glasses collected by the submersible Alvin from the southern Juan de Fuca Ridge (SJFR) are almost identical (/sup 206/Pb//sup 204/Pbapprox.18.45, /sup 207/Pb//sup 204/Pbapprox.15.47, /sup 208/Pb//sup 204/Pbapprox.37.81, /sup 87/Sr//sup 86/Srapprox.0.70249, /sup 143/Nd//sup 144/Ndapprox.0.51315). Whereas all basalts appear cogenetic, four of the samples have uniform abundances of U, Th, Rb, Nd, Sm, Pb, and Sr, indicating that they are also comagmatic. Two basalt glasses dredged previously at the SJFR have similar isotopic compositions but higher concentrations of U, Th, and Pb. The /sup 206/Pb//sup 204/Pb ratios are intermediate between generally less radiogenic ridge basalts from south of the Juan de Fuca Ridge (JFR) and often more radiogenic basalts from the northern JFR and NE Pacific seamounts. Sr and Nd isotopic compositions closely resemble data of other ridge basalts from the northernmost East Pacific Rise and are intermediate between isotopically more diverse seamount basalts produced nearby.

  17. Mesozoic vein-type Pb-Zn mineralization in the Pyrenees: Lead isotopic and fluid inclusion evidence from the Les Argentières and Lacore deposits

    NASA Astrophysics Data System (ADS)

    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.

  18. A study of REE and Pb, Sr and Nd isotopes in garnet-lherzolite xenoliths from Mingxi, Fujian Province

    USGS Publications Warehouse

    Wankang, H.; Junwen, W.; Basu, A.R.; Tatsumoto, M.

    1993-01-01

    The REE and Pb, Sr, Nd isotopes in three xenoliths from limburgite and scoria-breccias, including spinel-lherzolite, spinel-garnet-lherzolite and phlogopite-gamet-lherzolite, were analysed. The REE contents of the xenoliths are 1.3 to 3.3 times those of the chondrites with their REE patterns characterized by weak LREE depletion. The143Nd/144Nd values of whole rocks and minerals range from 0.51306 to 0.51345 with ??Nd=+ 8.2- +15.8,206Pb/204 Pb < 18.673, and207Pb/204Pb < 15.574. All this goes to show that the upper mantle in Mingxi at the depth of 67-82 km is a depleted mantle of MORB type, with87Sr/86 Sr ratios 0.70237-0.70390. In Nd-Sr diagram the data points of whole rocks are all out of the mantle array, implying that the xenoliths from Mingxi have more radiogenic Sr isotopes than those of the mantle array. ?? 1993 Institute of Geochemistry, Chinese Academy of Sciences.

  19. Early Cretaceous (ca. 100 Ma) magmatism in the southern Qiangtang subterrane, central Tibet: Product of slab break-off?

    NASA Astrophysics Data System (ADS)

    Li, Yalin; He, Haiyang; Wang, Chengshan; Wei, Yushuai; Chen, Xi; He, Juan; Ning, Zijie; Zhou, Aorigele

    2016-09-01

    The lack of Early Cretaceous magmatic records with high-quality geochemical data in the southern Qiangtang subterrane has inhibited a complete understanding of the magmatic processes and geological evolution of central Tibet. In this study, we present zircon U-Pb ages, whole-rock geochemistry, and Sr-Nd-Pb and zircon Hf isotopic data for the newly discovered Moku pluton in the southern Qiangtang subterrane. Zircon U-Pb dating reveals that the Moku granites were emplaced in the Early Cretaceous (ca. 100 Ma) and are coeval with the hosted dioritic enclaves. The granites are slightly peraluminous and high-K calc-alkaline I-type granites and characterized by initial (87Sr/86Sr)i ratios of 0.70605-0.70658, negative ɛ Nd(t) values (-4.44 to -3.35), and Nd isotopic model ages of 1.19-1.29 Ga. The granites have a wide range of zircon ɛ Hf(t) values (-24.4 to 2.6) and concordant ratios of (206Pb/204Pb)t = 18.645-18.711, (207Pb/204Pb)t = 15.656-15.666, and (208Pb/204Pb)t = 38.751-38.836. The coeval dioritic enclaves are medium- to high-K calc-alkaline rocks with zircon ɛ Hf(t) values of -13.3 to +3.6. The geochemical signatures of the host granites and coeval dioritic enclaves indicate that the Moku pluton was most likely generated by partial melting of the ancient lower crust with contributions from mantle-derived melts. Our new data, together with other recently published data, indicate that the ca. 100 Ma magmatic rocks were derived from anatexis of the Qiangtang lower crust that mixed with upwelling asthenosphere materials in response to the slab break-off of the northward subduction of the Bangong-Nujiang oceanic lithosphere.

  20. Lead isotopic studies of the Samail ophiolite, Oman

    SciTech Connect

    Chen, J.H.; Pallister, J.S.

    1981-04-10

    The isotopic composition of Pb and the concentrations of U, Th, and Pb have been determined for samples from various lithologic units and massive sulfides of the Samail ophiolite. The observed /sup 206/Pb//sup 204/Pb ratios range from 17.90 to 19.06, /sup 207/Pb//sup 204/Pb ratios from 15.43 to 15.63, and /sup 208/Pb//sup 204/Pb from 37.66 to 38.78. In Pb isotopic evolution diagrams, the initial Pb isotopic compositions of most of the samples from the Samail ophiolite plot within the field of oceanic basalt, clearly distinct from island arc data, and define some of the least radiogenic Pb observed from oceanic rocks. Lead data from the Samail are compatible with a model involving magma generation from an oceanic mantle source and formation of the ophiolite at an oceanic spreading center. U--Th--Pb isotopic systematics demonstrate that vertical heterogeneity in the oceanic crust can be created through differential concentration of U, Th, and Pb during crystal fractionation and alteration at, or near, the spreading ridge. Calcite form amygdules in the ophiolite basalt has similar Pb isotopic composition to the igneous rocks, suggesting precipitation of the calcite from seawater which contained Pb derived mostly from the oceanic crust. Lead isotopic data on Fe--Cu sulfides are also similar to the results from the igneous suite suggesting that the source of the sulfides is predominently from the oceanic crust. Lead data from serpentinized peridotite and a galena sample from below the ophiolite suggest that part of the serpentinization process and the formation of galena could involve addition of radiogenic Pb from either a continental source or from oceanic sediments.

  1. Stable lead isotopes reveal a natural source of high lead concentrations to gasoline-contaminated groundwater

    USGS Publications Warehouse

    Landmeyer, J.E.; Bradley, P.M.; Bullen, T.D.

    2003-01-01

    Concentrations of total lead as high as 1,600 ??g/L were detected in gasoline-contaminated and uncontaminated groundwater at three gasoline-release sites in South Carolina. Total lead concentrations were highest in turbid groundwater samples from gasoline-contaminated and uncontaminated wells, whereas lower turbidity groundwater samples (collected using low-flow methods) had lower total lead concentrations. Dissolved lead concentrations in all wells sampled, however, were less than 15 ??g total lead/L, the current United States Environmental Protection Agency (US EPA) maximum contaminant level (MCL). Because many total lead concentrations exceeded the MCL, the source of lead to the groundwater system at two of the three sites was investigated using a stable lead isotope ratio approach. Plots of the stable isotope ratios of lead (Pb) in groundwater as 207Pb/206Pb versus 208Pb/206Pb, and 208Pb/204Pb versus 206Pb/204Pb were similar to ratios characteristic of lead-based minerals in local rocks of the southeastern US, and were not similar to the stable lead isotopes ratios characteristic of distant lead ore deposits such as Broken Hill, Australia, used to produce tetraethyl lead in gasoline products prior to its phase-out and ban in the United States. Moreover, the isotopic composition of dissolved lead was equivalent to the isotopic composition of total lead in turbid samples collected from the same well, suggesting that the majority of the lead detected in the groundwater samples was associated with sediment particulates of indigenous aquifer material, rather than lead associated with spilled leaded gasoline. The results of this investigation indicate that (1) lead detected at some gasoline-release sites may be derived from the local aquifer material, rather than the gasoline release, and consequently may affect site-specific remediation goals; (2) non-low flow groundwater sampling methods, such as a disposable bailer, may result in turbid groundwater samples and

  2. Application of laser ablation multicollector inductively coupled plasma mass spectrometry for the measurement of calcium and lead isotope ratios in packaging for discriminatory purposes.

    PubMed

    Santamaria-Fernandez, Rebeca; Wolff, Jean-Claude

    2010-07-30

    The potential of high-precision calcium and lead isotope ratio measurements using laser ablation coupled to multicollector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) to aid distinction between four genuine and five counterfeit pharmaceutical packaging samples and further classification of counterfeit packaging samples has been evaluated. We highlight the lack of reference materials for LA-MC-ICP-MS isotope ratio measurements in solids. In this case the problem is minimised by using National Institute of Standards and Technology Standard Reference Material (NIST SRM) 915a calcium carbonate (as solid pellets) and NIST SRM610 glass disc for sample bracketing external standardisation. In addition, a new reference material, NIST SRM915b calcium carbonate, has been characterised in-house for Ca isotope ratios and is used as a reference sample. Significant differences have been found between genuine and counterfeit samples; the method allows detection of counterfeits and aids further classification of packaging samples. Typical expanded uncertainties for measured-corrected Ca isotope ratio values ((43)Ca/(44)Ca and (42)Ca/(44)Ca) were found to be below 0.06% (k = 2, 95% confidence) and below 0.2% for measured-corrected Pb isotope ratios ((207)Pb/(206)Pb and (208)Pb/(206)Pb). This is the first time that Ca isotope ratios have been measured in packaging materials using LA coupled to a multicollector (MC)-ICP-MS instrument. The use of LA-MC-ICP-MS for direct measurement of Ca and Pb isotopic variations in cardboard/ink in packaging has definitive potential to aid counterfeit detection and classification. PMID:20552700

  3. Application of laser ablation multicollector inductively coupled plasma mass spectrometry for the measurement of calcium and lead isotope ratios in packaging for discriminatory purposes.

    PubMed

    Santamaria-Fernandez, Rebeca; Wolff, Jean-Claude

    2010-07-30

    The potential of high-precision calcium and lead isotope ratio measurements using laser ablation coupled to multicollector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) to aid distinction between four genuine and five counterfeit pharmaceutical packaging samples and further classification of counterfeit packaging samples has been evaluated. We highlight the lack of reference materials for LA-MC-ICP-MS isotope ratio measurements in solids. In this case the problem is minimised by using National Institute of Standards and Technology Standard Reference Material (NIST SRM) 915a calcium carbonate (as solid pellets) and NIST SRM610 glass disc for sample bracketing external standardisation. In addition, a new reference material, NIST SRM915b calcium carbonate, has been characterised in-house for Ca isotope ratios and is used as a reference sample. Significant differences have been found between genuine and counterfeit samples; the method allows detection of counterfeits and aids further classification of packaging samples. Typical expanded uncertainties for measured-corrected Ca isotope ratio values ((43)Ca/(44)Ca and (42)Ca/(44)Ca) were found to be below 0.06% (k = 2, 95% confidence) and below 0.2% for measured-corrected Pb isotope ratios ((207)Pb/(206)Pb and (208)Pb/(206)Pb). This is the first time that Ca isotope ratios have been measured in packaging materials using LA coupled to a multicollector (MC)-ICP-MS instrument. The use of LA-MC-ICP-MS for direct measurement of Ca and Pb isotopic variations in cardboard/ink in packaging has definitive potential to aid counterfeit detection and classification.

  4. Late Cretaceous porphyry Cu and epithermal Cu-Au association in the Southern Panagyurishte District, Bulgaria: the paired Vlaykov Vruh and Elshitsa deposits

    NASA Astrophysics Data System (ADS)

    Kouzmanov, Kalin; Moritz, Robert; von Quadt, Albrecht; Chiaradia, Massimo; Peytcheva, Irena; Fontignie, Denis; Ramboz, Claire; Bogdanov, Kamen

    2009-08-01

    the magmas. 87Sr/86Sr(i) ratios of igneous rocks in the range of 0.70464 to 0.70612 and 143Nd/144Nd(i) ratios in the range of 0.51241 to 0.51255 indicate mixed crustal-mantle components of the magmas dominated by mantellic signatures. The epsilon Hf composition of magmatic zircons (+6.2 to +9.6) also suggests mixed mantellic-crustal sources of the magmas. However, Pb isotopic signatures of whole rocks (206Pb/204Pb = 18.13-18.64, 207Pb/204Pb = 15.58-15.64, and 208Pb/204Pb = 37.69-38.56) along with common inheritance component detected in magmatic zircons also imply assimilation processes of pre-Variscan and Variscan basement at various scales. U-Pb zircon and rutile dating allowed determination of the timing of porphyry ore formation at Vlaykov Vruh (85.6 ± 0.9 Ma), which immediately followed the crystallization of the subvolcanic dacitic bodies at Elshitsa (86.11 ± 0.23 Ma) and the Elshitsa granite (86.62 ± 0.02 Ma). Strontium isotope analyses of hydrothermal sulfates and carbonates (87Sr/86Sr = 0.70581-0.70729) suggest large-scale interaction between mineralizing fluids and basement lithologies at Elshitsa-Vlaykov Vruh. Lead isotope compositions of hydrothermal sulfides (206Pb/204Pb = 18.432-18.534, 207Pb/204Pb = 15.608-15.647, and 208Pb/204Pb = 37.497-38.630) allow attribution of ore-formation in the porphyry and epithermal deposits in the Southern Panagyurishte district to a single metallogenic event with a common source of metals.

  5. Pb, Nd, and Sr isotopic evidence for a multicomponent source for rocks of Cook-Austral Islands and heterogeneities of mantle plumes

    SciTech Connect

    Nakamura, Yoichi; Tatsumoto, Mitsunobu )

    1988-12-01

    Sr, Nd, and Pb isotopic compositions were measured in alkane volcanic rocks from the South Cook Islands and the Austral Islands. The results show that the Cook-Austral rocks have an extremely wide range in isotopic compositions of Pb: {sup 206}Pb/{sup 204}Pb from 18.25 to 21.76, {sup 207}Pb/{sup 204}Pb from 15.48 to 15.83, and {sup 208}Pb/{sup 204}Pb from 38.37 to 40.62, whereas isotopic compositions of Sr and Nd are less variable. Isotopically, Mangaia, Rimatara, and Rurutu form one group, which shows extremely ratiogenic Pb isotopic compositions but near-MORB (mid-ocean ridge basalts) values for Sr and Nd isotopic ratios. In contrast, samples from Aitutaki, Rarotonga, Mauke, and Atiu (Aitutaki group) have high {sup 207}Pb/{sup 204}Pb and {sup 208}Pb/{sup 204}Pb and moderately high {sup 87}Sr/{sup 86}Sr (Dupal anomaly). The Aitutaki group could have been derived from heterogeneous mantle plumes, which rose from the enriched deep mantle (the almost primitive lower mantle or recycled continental and oceanic slabs). On the other hand, the Mangaia component could have been derived from the depleted upper mantle which may have been metasomatized with a Co{sub 2}-rich fluid, as indicated by the near-MORB values of Sr and Nd isotopes. Although Pb isotopic data of the two groups cannot be distinguished from each other statistically, the end components of the Pb-Pb system do not match with those of the Nd-Sr system. Thus, the data must be explained by a multi-, at least three, component mixing model: the mantle plumes, metasomatized upper mantle, and lithosphere. The K-Ar ages and isotopic characteristics of the Cook-Austral rocks indicate that if one mantle plume rises from the deep mantle in this region, it has separated into at least two segments on the way to the surface.

  6. Pb, Nd, and Sr isotopic evidence for a multicomponent source for rocks of Cook-Austral Islands and heterogeneities of mantle plumes

    USGS Publications Warehouse

    Nakamura, Y.; Tatsumoto, M.

    1988-01-01

    Sr, Nd, and Pb isotopic compositions were measured in alkaline volcanic rocks (alkali basalt, ankaramite, nephelinite, phonolite, and trachyte) from the South Cook Islands (Aitutaki, Mauke, Rarotonga, Atiu, and Mangaia) and the Austral Islands (Rimatara and Rurutu). The results show that the Cook-Austral rocks have an extremely wide range in isotopic compositions of Pb: 206Pb 204Pb from 18.25 to 21.76, 207pb 204pb from 15.48 to 15.83, and sol208pb 204Pb from 38.37 to 40.62, whereas isotopic compositions of Sr and Nd are less variable. Isotopically, Mangaia, Rimatara, and Rurutu form one group (Mangaia group), which shows extremely radiogenic Pb isotopic compositions but near-MORB (mid-oceanic ridge basalts) values for Sr and Nd isotopic ratios. In contrast, samples from Aitutaki, Rarotonga, Mauke, and Atiu (Aitutaki group) have high 207Pb 204Pb and 208Pb 204Pb and moderately high 87Sr 86Sr (Dupal anomaly). The Aitutaki group could have been derived from heterogeneous mantle plumes, which rose from the enriched deep mantle (the almost primitive lower mantle or recycled continental and oceanic slabs). On the other hand, the Mangaia component could have been derived from the depleted upper mantle which may have been metasomatized with a CO2-rich fluid, as indicated by the near-MORB values of Sr and Nd isotopes. Although Pb isotopic data of the two groups cannot be distinguished from each other statistically, the end components of the Pb-Pb system do not match with those of the Nd-Sr system. Thus, the data must be explained by a multi-, at least three, component mixing model: the mantle plumes (Dupal component and a recycled oceanic slab), metasomatized upper mantle, and lithosphere. The K-Ar ages and isotopic characteristics of the Cook-Austral rocks indicate that if one mantle plume rises from the deep mantle in this region, it has separated into at least two segments on the way to the surface. ?? 1988.

  7. The geochemical components that distinguish Loa- and Kea-trend Hawaiian shield lavas

    NASA Astrophysics Data System (ADS)

    Frey, Frederick A.; Huang, Shichun; Xu, Guangping; Jochum, Klaus P.

    2016-07-01

    Recent (<5 Ma) Hawaiian volcanoes define two sub-parallel spatial trends, Loa and Kea. Despite the short distance (∼30 km) between adjacent volcanoes on these trends, most of the Loa-trend shield lavas are geochemically distinct from most of the Kea-trend shield lavas. These geochemical differences arise from small amounts of the LOA component in the source of Loa-trend shield lavas. This component is most prominent in the uppermost shield lavas of Koolau, Lanai and Kahoolawe volcanoes. Correlations between abundance ratios of incompatible elements and isotopic ratios of Sr, Nd, Hf and Pb in Hawaiian shield lavas indicate that the LOA component consists of three geochemically distinct materials formed by diverse processes. A gabbroic adcumulate (i.e. no trapped melt) with abundant cumulus plagioclase is responsible for the high Sr/Nd, La/Th and La/Nb in Loa-trend shield lavas relative to Kea-trend shield lavas. Also it has relatively low 206Pb/204Pb and high 208Pb/204Pb at a given 206Pb/204Pb, consistent with the low U/Pb and Th/Pb that are characteristic of plagioclase; these distinctive Pb isotope ratios require a long-time interval, ∼3 Ga, to develop. This material is most abundant in the uppermost shield lavas of Koolau volcano. Possible origins of adcumulate gabbros with abundant cumulus plagioclase are the lower oceanic and continental crust. A second material in the LOA component is distinctive because it is offset from the linear trend of 176Hf/177Hf versus 143Nd/144Nd, known as the terrestrial array, to high 176Hf/177Hf at low 143Nd/144Nd. This offset requires an ancient material with high Lu/Hf. It is equally abundant in the shield lavas at Koolau, Lanai and Kahoolawe volcanoes. Possible origins of this material are ancient pelagic sediment or ancient depleted lithosphere. A third material in the LOA component is characterized by relatively high 87Sr/86Sr, but the Rb/Sr of this material is too low to explain the high 87Sr/86Sr in 4.5 Ga. A relatively

  8. Monthly-resolved coral skeletal lead isotopic determination in picogram quantities by MC-ICP-MS

    NASA Astrophysics Data System (ADS)

    Chou, Y.; Shen, C.; Lo, Y.; Chang, C.

    2011-12-01

    Pb concentrations and isotopic composition in coral skeletons have been applied to understanding annual-decadal trends of natural hydrological evolution, ocean circulation, and anthropogenic pollution. However, the low Pb contents of only 10s-100s ng/g has hindered measurements of monthly-resolved coral Pb isotopic records and limited its applications. We refined chemistry and improved instrumental methodology to develop a reliable procedure for picogram-quantity coral Pb isotopic determination (Pb-204, Pb-206, Pb-207, and Pb-208) on a multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS, Thermo Electron NEPTUNE). The overall procedural blank is <20 pg. Replicate measurements made on standard NIST SRM 981 shows that our method can achieve a precision of ± 300 ppm (2σ) for Pb-207/Pb-206 and Pb-208/Pb-206 with 100s-1000s pg of Pb. Monthly-resolution Pb isotopic and concentration records of a coral Porites collected by Son Tra Island, central Vietnam (16°12'59.4", 108°1'57.1") from 1978-2004 AD have been measured. Three features are exhibited as follows: (1) The high Pb/Ca background level of 0.652 μmol/mol after 1992, 1.5 times larger than value of 0.437 μmol/mol in 1978-1992, shows an impact of economic development on hydrological change. (2) Ratios of Pb-208/Pb-207, Pb-206/Pb-207, and Pb-206/Pb-204 are relatively low in winter and high in summer, reflecting different seasonal sources. (3) Significant Pb isotopic anomalies in 1991-1992 could result from the eruption of Mt. Pinatubo on June 15, 1991. Our results indicate that monthly-resolved coral Pb isotopic and concentration can be used as proxies of seasonal climate changes, volcanic impacts and humanity activities.

  9. 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.

    PubMed

    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.

  10. 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

    NASA Astrophysics Data System (ADS)

    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 (12.8<δ34S<14.0 ‰). The δ34S values for sulfides of the both study area range from 2.6 to 9.5 ‰. These positive δ34S values are likely due to abiotic thermally-driven abiotic sulfate reduction (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.

  11. Mt. St. Augustine, Alaska: Geochemical evolution of an eastern Aleutian volcanic center

    SciTech Connect

    Johnson, K.E. . Dept. of Geology); Harmon, R.S. . Kingsley Dunham Centre); Moorbath, S. . Dept. of Earth Sciences); Sigmarsson, O. )

    1993-04-01

    Mt. St. Augustine is a calc-alkaline Quaternary volcano, situated within Cook Inlet, Alaska. The island is composed of low- to medium-K andesite and dacite domes and pyroclastic flows. Major element variations indicate the magmatic evolution is dominantly influenced by fractionation and magma-mixing processes. Incompatible element and isotopic compositions suggest that despite its continental location, crustal assimilation is not significant factor in magmatic evolution. Alkali contents for Augustine are generally lower than elsewhere in the Aleutians (e.g. Augustine Cs/Rb = 0.016--0.024, K/Rb = 372--553; Aleutians Cs/Rb = 0.016--0.17, K/Rb = 231--745). Sr- and Nd-isotope ratios encompass narrow ranges ([sup 87]Sr/[sup 86]Sr = 0.70317--0.70343; [sup 143]Nd/[sup 144]Nd = 0.513011--0.513085), characteristic of uncontaminated mantle-derived melts. U-Th disequilibrium isotopic values also indicate little or no assimilation of evolved continental crust. Pb-isotopic ranges are also relatively restricted ([sup 206]Pb/[sup 204]Pb = 18.62--18.82; [sup 207]Pb/[sup 204]Pb = 15.54--15.57; [sup 208]Pb/[sup 204]Pb = 38.18--38.34) and comparison with north Pacific enriched (OIB) and depleted (MORB) mantle sources suggest the incorporation of only a small percentage of subducted terrigenous sediments. A model for Augustine magma genesis is proposed where parental magmas are generated by 5--20% partial melting of a lherzolite mantle with up to a 5% subducted terrigenous sediment component. The major influence of the thickened continental crust is to prevent the ascent and eruption of basaltic magma. The data exhibit no temporal variations, indicating that the magmatic system which produced the historic eruptions is well established.

  12. Petrogenesis and tectonic setting of the early Mesozoic Xitian granitic pluton in the middle Qin-Hang Belt, South China: Constraints from zircon U-Pb ages and bulk-rock trace element and Sr-Nd-Pb isotopic compositions

    NASA Astrophysics Data System (ADS)

    Wu, Qianhong; Cao, Jingya; Kong, Hua; Shao, Yongjun; Li, Huan; Xi, Xiaoshuang; Deng, Xuantong

    2016-10-01

    The Xitian pluton in southeast Hunan province is one of the early Mesozoic (Indosinian) granitic plutons in the South China Block. It is composed of biotite adamellite with K-feldspar megacrysts, biotite adamellite, and biotite granite that have U-Pb zircon ages of 229.9 ± 1.4 Ma, 223.6 ± 1.3 Ma, and 224.0 ± 1.4 Ma, respectively. The Indosinian granitoids in the Xitian pluton belong to S-type granites, with highly radiogenic initial 87Sr/86Sr ratios (0.71397-0.71910), negative εNd(t) values ranging from -10.1 to -9.4, and old Nd model ages (1858-1764 Ma). They are enriched in radiogenic Pb isotopes, with (206Pb/204Pb)t ranging from 18.130 to 18.903, (207Pb/204Pb)t from 15.652 to 15.722, and (208Pb/204Pb)t from 38.436 to 39.037, respectively. These features indicate that the granitoidswithin the Xitian pluton were formed from magmas generated by remelting of metapelite and metapsammite of the Paleoproterozoic metamorphic basement at temperatures of ca. 800 °C, with low oxygen fugacity. The Sr-Nd isotopic compositions of the rocks from Xitian pluton indicate that the granitic magmas were mixed with less than 10% mantle-derived magmas. We suggest that the Xitian pluton was emplaced in an extensional tectonic setting related to release of compressional stresses within the thickened crust during the early Mesozoic.

  13. Chemical constraints on the petrogenesis of mildly alkaline lavas from Vestmannaeyjar, Iceland: the Eldfell (1973) and Surtsey (1963 1967) eruptions

    NASA Astrophysics Data System (ADS)

    Furman, Tanya; Frey, Fred A.; Park, Kye-Hun

    1991-03-01

    The Vestmannaeyjar archipelago is composed of alkalic lavas erupted at the southern end of the active, southward propagating, Eastern Volcanic Zone. Recent eruptions include the most primitive (Surtsey) and most evolved (Eldfell) compositions found in this area. We studied time-stratigraphic sample suites from both eruptions to characterize the magmatic environment of Vestmannacyjar. All samples are nearly homogeneous in radiogenic isotopic ratios (87Sr/86Sr 0.70304 to 0.70327;143Nd/144Nd 0.51301 to 0.50307;206Pb/204Pb 18.96 to 19.18;207Pb/204Pb 15.50 to 15.53;208Pb/204Pb 38.47 to 38.76; KH Park and A Zindler, in preparation). Compositional trends of lavas from the two eruptions are not consistent with fractionation in a near-surface environment, but indicate rather moderate pressure evolution of small magma batches. At Eldfell, mugearite lavas can be modeled by 30% closed-system fractional crystallization of olivine+plagioclase+clinopyroxene+Fe-Ti oxides from parental hawaiite. The phase proportions are consistent with an experimentally determined moderate pressure (8 kbar) cotectic in mildly alkaline systems (Mahood and Baker 1986). Compositional variations of Surtsey lavas can be modeled by crystallization of clinopyroxene+olivine+plagioclase+minor Fe-Ti oxides. The presence of sodic plagioclase megacrysts and clinopyroxene with ˜8 wt% Al2O3 in xenoliths from Surtsey lavas are consistent with a moderate pressure fractionation event. Based on major-element and REE data the most primitive Surtsey lavas formed by small degrees of melting of a lherzolite source. The alkaline nature of Vestmannaeyjar lavas is not the result of assimilation of lower crustal melts (cf. Oskarsson et al. 1985; Steinthorsson et al. 1985).

  14. Siliciclastic Ordovician to Silurian units of the Argentine Precordillera: Constraints on provenance and tectonic setting in the proto-Andean margin of Gondwana

    NASA Astrophysics Data System (ADS)

    Abre, P.; Cingolani, C. A.; Cairncross, B.; Chemale, F.

    2012-12-01

    A combination of petrography, geochemistry, Sm-Nd, Pb-Pb and U-Pb detrital zircon dating provide constraints to the provenance of Middle Ordovician to Early Silurian clastic sequences of the Precordillera s.s. as a part of the Cuyania terrane in western-central Argentina. The uniformity shown by the provenance proxies indicate that there were no important changes in the provenance within these units. A dominant upper crustal component is evident as well as a subordinate mafic input. Nd isotopes indicate ɛNd of -5.4, ƒSm/Nd -0.34 and TDM 1.57 Ga in average for all the units studied. Pb-isotope ratios display average values for 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb of 19.37, 15.86 and 39.43 respectively. Detrital zircon dating further constraints the input as being dominantly of Mesoproterozoic age (51-83%), but with contributions from Neoproterozoic-Lower Cambrian (9-31%), Middle Cambrian to Ordovician grains (recorded up to 7%), and Palaeoproterozoic (2-7%) sources. The combination of the different provenance approaches applied indicates that the Mesoproterozoic Cuyania terrane basement, and partially the Pampia terrane were the main sources. The new information provided for the Ordovician to Silurian clastic sequences permitted enhanced the known geochemical and isotopic dataset to constrain the tectonic evolution of the Cuyania terrane. The interpretation of the obtained data supports that the terrane accretion to the proto-Andean margin of Gondwana probably occurred during Middle to early Upper Ordovician.

  15. Geochemistry of A-type granites in the Huangshaping polymetallic deposit (South Hunan, China): Implications for granite evolution and associated mineralization

    NASA Astrophysics Data System (ADS)

    Li, Huan; Watanabe, Koichiro; Yonezu, Kotaro

    2014-07-01

    The Huangshaping granites in Hunan Province, South China were investigated for their geochemical characteristics. Three types of granites have been petrographically identified: quartz porphyry, granophyre, and granite porphyry. Whole rock geochemistry suggests that the Huangshaping granites, especially the granite porphyry, exhibit typical A-type granite characteristics with their enrichment in Si, Rb, U, Th, and Nb and significant depletion in Ba, Sr, Ti, Eu, and P. Based on the Al, Y and Zr contents as well as the REE patterns of the rocks investigated, the quartz porphyry and the granophyre are classified as A1 type alkaline granites whereas the granite porphyry is considered as A2 type aluminous granite. Whole rock and quartz/feldspar O isotope data yields a wide range of δ18OSMOW values (11.09-26.32‰). The granites are characterized by high radiogenic Pb isotopic composition. The present-day whole rock Pb isotopic ratios are 206Pb/204Pb = 18.706-19.155, 207Pb/204Pb = 15.616-15.711 and 208Pb/204Pb = 38.734-39.296. Combining the O-Pb isotope compositions with major, trace and REE geochemistry and regional geology characteristics, the Huangshaping granites were determined to resemble within-plate granites that were mainly derived from a felsic infracrustal source related to continental extension. The magma source of the quartz porphyry and the granophyre may have been generated from deeper depths, and then ascended rapidly with limited water content and low oxygen fugacity, which contributed to Cu, Pb and Zn mineralization. On the other hand, the magma that generated the granite porphyry may have ascended relatively slower and experienced pronounced crystal fractionation, upper-crustal basement rock contamination (assimilation) and wall-rock interaction, producing the Sn- and W-rich granite porphyry. This study reveals the crustal extension process and associated magmatic-metallogenic activities during 180-150 Ma in South Hunan.

  16. Trace Metals, Rare Earths, Carbon and Pb Isotopes as Proxies of Environmental Catastrophe at the Permian - Triassic Boundary in Spiti Himalayas, India

    NASA Astrophysics Data System (ADS)

    Ghosh, N.; Basu, A. R.; Garzione, C. N.; Ghatak, A.; Bhargava, O. N.; Shukla, U. K.; Ahluwalia, A. D.

    2015-12-01

    Himalayan sediments from Spiti Valley, India preserve geochemical signatures of the Permian - Triassic (P-Tr) mass extinction in the Neo-Tethys Ocean. We integrate new sedimentological and fossil record with high-resolution geochemical-isotopic data from Spiti that reveals an ecological catastrophe of global proportions. Trace elements of U, Th, Nb, Ta, Zr, Hf, the rare earths (REE) and carbon, oxygen and lead isotopes measured across the P-Tr boundary in Spiti are used as proxies for evaluating abrupt changes in this continental shelf environment. δ13Corg excursions of 2.4‰ and 3.1‰ in Atargu and Guling P-Tr sections in Spiti Valley are associated with an abrupt fall of biological productivity while δ13Ccarb and δ18Ocarb record of these sediments shows effects of diagenesis. Here, the P-Tr boundary is compositionally distinct from the underlying Late Permian gray shales, as a partly gypsiferous ferruginous layer that allows additional geochemical-isotopic investigation of sedimentary sources. Conspicuous Ce - Eu anomalies in the light REE-enriched Late Permian shales reflect the source composition of the adjacent Panjal Trap basalts of Kashmir. An abrupt change of this source to continental crust is revealed by Nb - Ta and Zr - Hf anomalies at the P-Tr ferruginous layer and continuing through the overlying Early Triassic carbonate rocks. Pb concentration and isotope ratios of 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb identify changes in the sedimentary element flux, distinguishing the Late Permian shales from the distinct siliciclastic continental crustal signature in the Early Triassic carbonates. These geochemical-isotopic constraints on the sedimentary geochemistry of one of the most critical transitions in geological record establish the utility of multi-proxy datasets for paleoenvironmental reconstructions.

  17. Geochemical and geochronological constraints on the genesis of Au-Te deposits at Cripple Creek, Colorado

    USGS Publications Warehouse

    Kelley, K.D.; Romberger, S.B.; Beaty, D.W.; Pontius, J.A.; Snee, L.W.; Stein, H.J.; Thompson, T.B.

    1998-01-01

    compositions, together with major and trace element data, indicate that the phonolitic magmas probably evolved by fractional crystallization of an alkali basalt that assimilated lower crustal material. Upper crustal contamination of the magmas was not significant. The 206Pb/204Pb compositions of vein galenas almost entirely overlap those of phonolites, suggesting a genetic relationship between alkaline magmatism and mineralization. However, a trend toward higher 207Pb/204Pb (15.57-15.60) and 208Pb/204Pb ratios (38.94-39.48) of some galenas suggests a contribution to the ore fluid from surrounding Early Proterozoic rocks, probably through leaching by mineralizing fluids. Limited stable isotope compositions of quartz, K feldspar, and biotite from this and previous studies support a largely magmatic origin for the early vein fluids. It is suggested that three features were collectively responsible for generating alkaline magmas and associated mineral deposits: (1) the timing of magmatism and mineralization, which coincided with the transition between subduction-related compression and extension related to continental rifting; (2) the location of Cripple Creek at the junction of four major Precambrian units and at the intersection of major northeast-trending regional structures with northwest-trending faults, which served as conduits for magmas and subsequent hydrothermal fluids; and (3) the complex magmatic history which included emplacement of relatively felsic magmas followed by successively more mafic magmas with time.

  18. A composite, isotopically-depleted peridotite and enriched pyroxenite source for Madeira magmas: Insights from olivine

    NASA Astrophysics Data System (ADS)

    Gurenko, Andrey A.; Geldmacher, Jörg; Hoernle, Kaj A.; Sobolev, Alexander V.

    2013-06-01

    The Madeira and Canary island/seamount chains represent two adjacent hotspot tracks in the eastern North Atlantic, which were derived from mixed peridotite-pyroxenite mantle sources. They possess systematically different Sr-Nd-Pb, Os and Hf isotope signatures, implying mixing of DMM-, HIMU- and EM-type components from different mantle lithologies. The lithological nature of these postulated mantle endmembers (e.g., if formed by peridotite, pyroxenite and/or eclogite) is still a subject of debate. We studied the chemical composition of olivine phenocrysts (focusing on their Ni, Mn and Ca concentrations) from the lavas covering the entire volcanic history of the Madeira Archipelago (~ 0-5 Ma). We demonstrate that Ni × FeO/MgO and Mn/FeO ratios and Ca-concentrations of olivine correlate with Sr, Nd and Pb isotopic compositions of their host lavas. The amounts of peridotite- and pyroxenite-derived melt fractions in the parental Madeira magmas were inferred from olivine compositions and independently confirmed by modeling of two-component source melting using trace elements. Our calculations demonstrate that the amount of recycled crust (= eclogite) in the Madeira magma source varies but does not exceed ~ 10%. Strong linear relationships between chemical composition of olivine and radiogenic isotopes of the host lavas allow us to determine the isotopic composition of peridotite and pyroxenite endmembers of the Madeira hotspot. The peridotite endmember has a highly depleted isotopic composition 87Sr/86Sr = 0.7022-0.7026, 143Nd/144Nd = 0.5132-0.5135, 206Pb/204Pb = 17.4-18.6, 207Pb/204Pb = 15.4-15.49, and 208Pb/204Pb = 36.8-38.2, whereas the pyroxenite endmember has an enriched composition 87Sr/86Sr = 0.7031-0.7035, 143Nd/144Nd = 0.5127-0.5130, 206Pb/204Pb = 19.9-21.3, 207Pb/204Pb = 15.59-15.69, and 208Pb/204Pb = 39.6-41.2. Our new data confirm the existence of recycled (pyroxenitic) lithology in the Madeira magma source that was previously interpreted to represent

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

    PubMed

    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.

  20. Pb isotope geochemistry of Piton de la Fournaise historical lavas

    NASA Astrophysics Data System (ADS)

    Vlastélic, Ivan; Deniel, Catherine; Bosq, Chantal; Télouk, Philippe; Boivin, Pierre; Bachèlery, Patrick; Famin, Vincent; Staudacher, Thomas

    2009-07-01

    Variations of Pb isotopes in historical lavas (1927-2007) from Piton de la Fournaise are investigated based on new (116 samples) and published (127 samples) data. Lead isotopic signal exhibits smooth fluctuations (18.87 < 206Pb/ 204Pb < 18.94) on which superimpose unradiogenic spikes ( 206Pb/ 204Pb down to 18.70). Lead isotopes are decoupled from 87Sr/ 86Sr and 143Nd/ 144Nd, which display small and barely significant variations, respectively. No significant change of Pb isotope composition occurred during the longest (> 3 years) periods of inactivity of the volcano (1939-1942, 1966-1972, 1992-1998), supporting previous inferences that Pb isotopic variations occur mostly during and not between eruptions. Intermediate compositions (18.904 < 206Pb/ 204Pb < 18.917) bracket the longest periods of quiescence. In this respect, the highly frequent occurrence of an intermediate composition (18.90 < 206Pb/ 204Pb < 18.91), which clearly defines an isotopic baseline during the most recent densely sampled period (1975-2007), either suggests direct sampling of plume melts or sampling of a voluminous magma reservoir that buffers Pb isotopic composition. Deviations from this prevalent composition occurred during well-defined time periods, namely 1977-1986 (radiogenic signature), 1986-1990 and 1998-2005 (unradiogenic signatures). The three periods display a progressive isotopic drift ending by a rapid return (mostly during a single eruption) to the isotopic baseline. The isotopic gradients could reflect progressive emptying of small magma reservoirs or magma conduits, which are expected to be more sensitive to wall-rock interactions than the main magma chamber. These gradients provide a lower bound ranging from 0.1 to 0.17 km 3 for the size of the shallow magma storage system. The isotopic shifts (March 1986, January 1990 and February 2005) are interpreted as refilling the plumbing system with deep melts that have not interacted with crustal components. The volume of magma erupted

  1. Variations in Pb concentrations and Pb-isotope ratios in soils collected along an east-west transect across the United States

    NASA Astrophysics Data System (ADS)

    Smith, David; Woodruff, Laurel; Reimann, Clemens; Flem, Belinda

    2014-05-01

    Soil A-horizon and C-horizon samples were collected along a 4000 km long transect cutting the USA from the west to the east coast. For purposes of site selection, the transect was divided into approximately 40-km segments. For each segment, a 1-km2 target area was selected at random. Soil A- and C-horizon samples were collected at a site within each target area that was most representative of the surrounding landscape. The samples were air-dried at ambient temperature, disaggregated, and sieved through a 2-mm stainless steel screen. The <2-mm material was crushed to <150 µm in a ceramic mill prior to chemical analysis. Lead was analyzed in all the A- and C-horizon samples by inductively coupled plasma-mass spectrometry following a 4-acid digestion. The complete dataset can be found in Smith et al., 2005. Pb-isotope ratio measurements were carried out on 159 soil A-horizon and 137 soil C-horizon samples on an inductively coupled sector field plasma mass spectrometer (SF-ICP-MS; ELEMENT 1, Finnigan MAT) in the laboratory of the Geological Survey of Norway (NGU), following a 7 N HNO3 digestion. Lead concentrations along the transect show (1) generally higher values in the soil A-horizon than the C-horizon (median 21 vs. 16.5 mg/kg), (2) an increase in the median value of the soil A-horizon for the central to eastern U.S. (Missouri to Maryland) when compared to the western U.S. (California to Kansas) (median 26 vs. 20 mg/kg) and (3) a higher A/C ratio for the central to eastern US (1.35 vs. 1.14). Lead isotopes show a distinct trend across the U.S., with the highest 206Pb/207Pb ratios occurring in the centre (Missouri, median A-horizon: 1.245; C-horizon: 1.251) and the lowest at both coasts (e.g. California, median A-horizon: 1.195; C-horizon:1.216). The soil C-horizon samples show generally higher 206Pb/207Pb ratios than the A-horizon (median C-horizon: 1.224; A-horizon: 1.219). The 206Pb/207Pb isotope ratios in the soil A horizon show a correlation with the total

  2. K-Ar ages and Pb, Sr isotopic characteristics of Cenozoic volcanic rocks in Shandong Province, China

    USGS Publications Warehouse

    Daogong, C.; Zicheng, P.; Lanphere, M.A.; Zartman, R.E.

    1985-01-01

    28 samples of Cenozoic volcanic rocks collected from Shandong Province have been dated by K-Ar method. They are mainly Neogene with an age range of 4-19 m. y. The basalts from Linqu and Yishui in west Shandong Province are Miocene and those from Penglai and Qixia in east Shandong Province are Miocene and Pliocene in age. The basalts from Wudi in north Shandong Province are Middle-Early Pleistocene in age. In each area the duration of volcanic eruption was estimated at about 2-3 m. y. Pb and Sr isotopic compositions and U, Th, Pb, Rb, Sr, and major elements in most of the samples were determined. The isotopic compositions are:206Pb/204Pb-16.92-18.48,207Pb/204Pb-15.30-15.59,208Pb/204Pb-37.83-38.54, and (87Sr/86Sr)i-0.70327-0.70632. There are some positive or negative linear correlations between206Pb/204Pb and207Pb/204Pb, Pb isotopes and Pb content, Pb isotopes and Sr isotopes, and Sr isotopes and other elements. The basaltic rocks from east and west Shandong Province have somewhat differences in isotopic composition and element content. The basalts probably are products of multi-stage evolution of the mantle. They have preserved the primary features of the source, although they were influenced, to some extent, by the contamination of crustal materials. ?? 1985 Institute of Geochemistry, Chinese Academy of Sciences.

  3. Petrogenesis of pillow basalts from Baolai in southwestern Taiwan

    NASA Astrophysics Data System (ADS)

    Liu, Chih-Chun; Yang, Huai-Jen

    2016-04-01

    The pillow basalts from Baolai in southwestern Taiwan have been inferred to bear Dupal signautres based on their Th/Ce ratio, linking the Baolai basalts to the South China Sea (SCS) seamounts that are characterized by Dupal Pb isotope signatures (Smith and Lewis, 2007). In this study, thirty-two Baolai basalt samples were analyzed for abundances of major and trace elements as well as Pb and Nd isotope ratios to verify their Dupal characters and to constrain their petrogenesis significance. The Baolai basalts contain 4-10 % L.O.I.. Three stages of alteration are inferred from plots of L.O.I. abundance versus concentrations major oxides as well as mineral textures and compositions. The first alteration stage was characterized by albitization that converted Ca-rich plagioclase to albite. The second alteration stage was dominated by chloritization of olivine and augite, resulting in increases in L.O.I. abundance. The last alteration stage is represented by formation of secondary calcite in vesicles and cracks. These alteration processes reflect interaction with seawater and apparently did not affect the magmatic Pb isotope composition for the low Pb concentration in seawater. Relative to the North Hemisphere Reference Line (NHRL), the Baolai pillow basalts have higher 208Pb/204Pb ratios at a given 206Pb/204Pb value, showing Dupal anomaly. For their relatively higher 208Pb/204Pb, 207Pb/204Pb, and 206Pb/204Pb ratios, the Baolai basalts are distinct from majority of the Cenozoic basalts in the Hainan-Leizhou peninsula, the Indochina peninsula, and the SCS seamounts, for which derivation from the Hainan mantle plume has been recently proposed (Wang et al., 2013). In contrast, the Baolai basalts and the Cenozoic basalts from eastern Guangdong at southeastern China have similar Pb and Nd isotope compositions, indicating derivation from similar mantle sources. However, the Baolai basalts have lower abundance ratios of Zr/Hf (40.3-45.6 versus 46.5-50.5), La/Yb (12

  4. Accurate and precise Pb isotope ratio measurements in environmental samples by MC-ICP-MS

    NASA Astrophysics Data System (ADS)

    Weiss, Dominik J.; Kober, Bernd; Dolgopolova, Alla; Gallagher, Kerry; Spiro, Baruch; Le Roux, Gaël; Mason, Thomas F. D.; Kylander, Malin; Coles, Barry J.

    2004-04-01

    Analytical protocols for accurate and precise Pb isotope ratio determinations in peat, lichen, vegetable, chimney dust, and ore-bearing granites using MC-ICP-MS and their application to environmental studies are presented. Acid dissolution of various matrix types was achieved using high temperature/high pressure microwave and hot plate digestion procedures. The digests were passed through a column packed with EiChrom Sr-resin employing only hydrochloric acid and one column passage. This simplified column chemistry allowed high sample throughput. Typically, internal precisions for approximately 30 ng Pb were below 100 ppm (+/-2[sigma]) on all Pb ratios in all matrices. Thallium was employed to correct for mass discrimination effects and the achieved accuracy was below 80 ppm for all ratios. This involved an optimization procedure for the 205Tl/203Tl ratio using least square fits relative to certified NIST-SRM 981 Pb values. The long-term reproducibility (+/-2[sigma]) for the NIST-SRM 981 Pb standard over a 5-month period (35 measurements) was better than 350 ppm for all ratios. Selected ore-bearing granites were measured with TIMS and MC-ICP-MS and showed good correlation (e.g., r=0.999 for 206Pb/207Pb ratios, slope=0.996, n=13). Mass bias and signal intensities of Tl spiked into natural (after matrix separation) and in synthetic samples did not differ significantly, indicating that any residual components of the complex peat and lichen matrix did not influence mass bias correction. Environmental samples with very different matrices were analyzed during two different studies: (i) lichens, vegetables, and chimney dust around a Cu smelter in the Urals, and (ii) peat samples from an ombrotrophic bog in the Faroe Islands. The presented procedure for sample preparation, mass spectrometry, and data processing tools resulted in accurate and precise Pb isotope data that allowed the reliable differentiation and identification of Pb sources with variations as small as 0

  5. U-Th-Pb and Rb-Sr systematics of Allende and U-Th-Pb systematics of Orgueil

    USGS Publications Warehouse

    Tatsumoto, M.; Unruh, D.M.; Desborough, G.A.

    1976-01-01

    U-Th-Pb systematics study of Allende inclusions showed that U, Th and Sr concentrations in Ca, Al (pyroxene)-rich chondrules and white and pinkish-white aggregate separates of Allende are five to ten times higher than those of the matrix, whereas Mg (olivine)-rich chondrules have U and Th concentrations about twice as high as the matrix. Th concentrations are extremely high in white aggregates and in pinkish-white (spinel-rich) aggregates while U and Sr concentrations in white aggregates are more than twice as high as those in pinkish-white aggregates. Large enrichment of these refractory elements in the white aggregates indicates that they contain high-temperature condensates from the solar nebula. The Pb concentrations in the inclusions are less than half of those in the whole rock and matrix, indicating that the matrix is a lower-temperature condensate. The isotopic composition of lead in the matrix is less radiogenic than that of the whole meteorite, whereas lead in Ca- and Al-rich chondrules and aggregates is extremely radiogenic. The 206Pb/204Pb ratio reaches as high as 55.9 in a white aggregate separate. The lead of Mg-rich chondrules is moderately radiogenic and the 206Pb/204Pb ratio ranges from 18 to 26. A striking linear relationship exists among leads in the chondrules, aggregates and matrix on the 207Pb/204Pb vs 204Pb/204Pb plot. The slope of the best fit line is 0.6188 ?? 0.0016, yielding an isochron age of 4553 ?? 4 m.y. The regression line passes through primordial lead values obtained from Canyon Diablo troilite. The data, when corrected for Canyon Diablo troilite Pb and plotted on a U-Pb concordia diagram, show that the pink and white aggregates and the Ca-Al-rich and Mg-rich inclusions have excess Pb and define a chord which intersects the concordia curve at 4548 ?? 25 m.y. and 107 ?? 70 m.y. The intercepts might correspond to the agglomeration age of the meteorite and a time of probably later disturbance, respectively. The matrix and some

  6. Lead atmospheric deposition rates and isotopic trends in Asian dust during the last 9.5 kyr recorded in an ombrotrophic peat bog on the eastern Qinghai-Tibetan Plateau

    NASA Astrophysics Data System (ADS)

    Ferrat, Marion; Weiss, Dominik J.; Dong, Shuofei; Large, David J.; Spiro, Baruch; Sun, Youbin; Gallagher, Kerry

    2012-04-01

    A full understanding of the atmospheric Pb cycle in Asia during the Holocene is key to palaeoclimate studies of past atmospheric circulation patterns, as well as to assess the impact of increasing industrial activities in this region. However, long-term records of atmospheric Pb isotopic trends in Asia are still sparse. Consequently, we study changes in the concentrations, fluxes and isotopic signature of deposited Pb contained in a 14C-dated peat core from the eastern Qinghai-Tibetan Plateau, dating back to 9.5 kyr BP, and present the first peat record of the changing isotopic composition of atmospheric Pb in dust in Asia during this time. Lead concentrations and fluxes vary between 2.96-21.58 μg g-1 and 0.06-3.52 mg m-2 y-1, respectively, with an average Pb baseline of 6.80 ± 4.18 μg g-1. These values agree with other Pb studies of lake and peat archives in China but are one order of magnitude larger than early and mid-Holocene values measured in Europe. Lead isotopic variability throughout the core is small, varying between 206Pb/207Pb = 1.190-1.197, 206Pb/204Pb = 18.648-18.786, 207Pb/204Pb = 15.666-15.694 and 208Pb/204Pb = 38.890-39.090. The application of Bayesian trans-dimensional changepoint modelling to the Pb dataset enabled the identification of eight significant changes in the isotopic composition of the deposited Pb. Such changes mark different phases of atmospheric Pb deposition, and hence variations in atmospheric circulation patterns and environmental conditions. Temporal variations in the potential natural and/or anthropogenic Pb sources are assessed based on the 206Pb, 207Pb, 208Pb and 204Pb isotopic composition and the 1/[Pb] ratio of the peat samples. Our results suggest that Pb deposition throughout the Holocene was governed by local deposition and long-range input from natural dust sources in northwestern (Taklamakan desert and Qaidam basin) and northern China (Badain Jaran and Tengger deserts). Input from the northern sources seems to have

  7. A lead isotopic study of the Stillwater Complex, Montana: constraints on crustal contamination and source regions

    USGS Publications Warehouse

    Wooden, J.L.; Czamanske, G.K.; Zientek, M.L.

    1991-01-01

    Analyses of the Pb isotopic compositions of plagioclase from 23 samples covering the stratigraphic thickness of the Stillwater Complex indicate a narrow range of apparent initial isotopic compositions (206Pb/ 204Pb=13.95; 207Pb/204Pb=14.95-15.01; 208Pb/204Pb=33.6). The uniformity of our data is in contrast to, but not necessarily contradictory to, other recent investigations which give indications that the complex formed by repeated injection of magmas with at least two distinct compositions that were presumably derived from different source regions. Samples from the Basal series of the complex have consistently higher 207Pb/204Pb ratios, suggesting either minor contamination from adjacent country rocks or a slight distinction between parental magmas. Apparent initial Pb isotopic compositions of the complex are very radiogenic compared to Late Archean model-mantle values, but are nearly identical to initial Pb isotopic compositions found for the the adjacent, slightly older (2.73-2.79 Ga), Late Archean crustal suite in the Beartooth Mountains. Contamination of magmas parental to the Stillwater Complex by the Late Archean crustal suite is rejected for two reasons: (1) Th and U concentrations in Stillwater rocks and plagioclase are very low (about 0.08 and 0.02 ppm respectively), yet Th/U ratios are uniform at about 4, in contrast to the highly variable (2-26) but often high Th/U ratios found for the Late Archean crustal complex; (2) it seems improbable that any contamination process would have adjusted the isotopic compositions of the diverse magmas entering the Stillwater chamber to near-identical values. The preferred hypothesis to explain the Pb isotopic data for the Stillwater Complex and the associated Late Archean crustal suite involves a major Late Archean crust-forming event that resulted in a compositionally complex crust/mantle system with relatively homogeneous and unusual Pb isotopic compositions. The parental magmas of the Stillwater Complex were

  8. The Condor seamount at Mid-Atlantic Ridge as a supplementary source of trace and rare earth elements to the sediments

    NASA Astrophysics Data System (ADS)

    Caetano, Miguel; Vale, Carlos; Anes, Bárbara; Raimundo, Joana; Drago, Teresa; Schimdt, Sabine; Nogueira, Marta; Oliveira, Anabela; Prego, Ricardo

    2013-12-01

    The Condor Seamount rises from seabed to 180m water depth, being located 10 nautical miles southwest of the island of Faial, Azores Archipelago at the Mid-Atlantic Ridge (MAR). The vertical distribution of major, minor, trace and rare earth elements (REE) and Pb isotopes was studied in four sediment cores: one from the top of the Condor Seamount (200m, MC9), two from the seamount base (1400m, MC2 and MC4), and one from a deep area (1900m, MC8). Sediments from the top of the Condor were composed by coarser particles being the fine fraction lower than 1%. Conversely the other sediments were constituted by 51-92% of fine particles (<63μm). Individual fragments of volcanic material (>2mm) were found at several depths of the cores sampled at the base of the seamount. The core collected in the top of the Condor showed higher carbonate content (76-86%) compared with the other cores (41-64%). The chemical compositions of MC2 and MC4 point to an enhancement of V, Cr, Co, Ni and Fe concentrations. Lower concentrations in MC8 hypothesis that Condor seamount constitutes a supplementary source of trace elements. The most plausible explanation for the enhancement found in sediments of the seamount base is the weathering of slopes with volcanic activities, which supply particles with higher element concentrations than pelagic sediments. This hypothesis is corroborated by REE data, showing increased chondrite normalized ratios in MC2 and MC4. Moreover, the REE pattern found in those cores was comparable to that existing in volcanic material with Light REE enrichment in comparison to Heavy REE. These results indicate a substantial contribution of particles derived from volcanic activities to sediments settled in the vicinity of the Condor Seamount. It is argued the potential use of REE in sediments from this region as tracers of volcanic activities. Depth profiles of 206Pb/207Pb and 206Pb/208Pb showed lower ratios in the first 8cm sediment layers, reflecting atmospheric input of

  9. Ancient Pb and Ti mobilization revealed by Scanning Ion Imaging

    NASA Astrophysics Data System (ADS)

    Kusiak, Monika A.; Whitehouse, Martin J.; Wilde, Simon A.

    2014-05-01

    Zircons from strongly layered early Archean ortho- and paragneisses in ultra-high temperature (UHT) metamorphic rocks of the Napier Complex, Enderby Land, East Antarctica are characterized by complex U-Th-Pb systematics [1,2,3]. A large number of zircons from three samples, Gage Ridge, Mount Sones and Dallwitz Nunatak, are reversely discordant (U/Pb ages older than 207Pb/206Pb ages) with the oldest date of 3.9 Ga [4] (for the grain from Gage Ridge orthogneiss). To further investigate this process, we utilized a novel high spatial resolution Scanning Ion Imaging technique on the CAMECA IMS 1280 at the Natural History Museum in Stockholm. Areas of 70 μm x 70 μm were selected for imaging in mono- and multicollection modes using a ~2 μm rastered primary beam to map out the distribution of 48Ti, 89Y, 180Hf, 232Th, 238U, 204Pb, 206Pb and 207Pb. The ion maps reveal variable distribution of certain elements within analysed grains that can be compared to their CL response. Yttrium, together with U and Th, exhibits zonation visible on the CL images, Hf shows expected minimal variation. Unusual patchiness is visible in the map for Ti and Pb distribution. The bright patches with enhanced signal do not correspond to any zones or to crystal imperfections (e.g. cracks). The presence of patchy titanium is likely to affect Ti-in-zircon thermometry, and patchy Pb affecting 207Pb/206Pb ages, usually considered as more robust for Archean zircons. Using the WinImage program, we produced 207Pb/206Pb ratio maps that allow calculation of 207Pb/206Pb ages for spots of any size within the frame of the picture and at any time after data collection. This provides a new and unique method for obtaining age information from zircon. These maps show areas of enhanced brightness where the 207Pb/206Pb ratio is higher and demonstrate that within these small areas (μm scale) the apparent 207Pb/206Pb age is older, in some of these patches even > 4 Ga. These data are a result of ancient Pb

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

    PubMed

    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

  11. Tracing the origin of pollution in French Alpine snow and aerosols using lead isotopic ratios.

    PubMed

    Veysseyre, A M; Bollhöfer, A F; Rosman, K J; Ferrari, C P; Boutron, C F

    2001-11-15

    Fresh snow samples collected at 15 remote locations and aerosols collected at one location in the French Alps between November 1998 and April 1999 have been analyzed for Pb concentration and isotopic composition by thermal ionization mass spectrometry. The snow samples contained 19-1300 pg/g of Pb with isotopic ratios 206Pb/207Pb (208Pb/207Pb) of 1.1279-1.1607 (2.3983-2.4302). Airborne Pb concentrations at one sampling site ranged from 0.42 to 6.0 ng/m3 with isotopic ratios of 1.1321-1.1427 (2.4029-2.4160). Air mass trajectory analysis combined with isotopic compositions of potential source regions did not show discernible evidence of the long-range atmospheric transport of pollutants. Isotopic ratios in the Alpine snow samples and thus the free troposphere were generally higher than airborne Pb isotopic ratios in urban France, which coupled with the relatively high Pb concentrations suggested a regional anthropogenic Pb source, probably Italy but possibly Eastern Europe.

  12. Constraints on slab inputs and mantle source compositions in the northern Cascade arc (Garibaldi belt) from Sr-Nd-Pb-Hf isotopes and trace elements in primitive basalts

    NASA Astrophysics Data System (ADS)

    Mullen, E. K.; Carpentier, M.; Weis, D.

    2011-12-01

    The northernmost segment of the Cascade arc, known as the Garibaldi volcanic belt (GVB), extends from Glacier Peak in Washington to the Bridge River cones in British Columbia. GVB primitive basalts display strong arc-parallel geochemical gradients, most prominently a northerly progression from calc-alkaline to highly alkalic compositions, which present an ideal opportunity to address key questions regarding the origin of primary arc basalts including the compositions and relative inputs of sub-arc mantle sources and slab-derived fluids/melts. The gradient in GVB basalt alkalinity was proposed to result from a northerly reduction in slab-derived contributions to the sub-arc mantle wedge, a consequence of the ~4 myr decrease in slab age at the trench [1-3]. As a test of this hypothesis, we have obtained new whole-rock high-precision isotopic (Sr, Nd, Pb, Hf) and trace element data for the GVB basalt suites previously investigated by Green and others. La/Nb decreases from south (4.25 at Glacier Peak) to north (0.78 at Bridge River), confirming a progressive reduction in the "arc signature" (elevated LILE and LREE abundances relative to HFSE and HREE). 87Sr/86Sr ranges from 0.70310 to 0.70396, 206Pb/204Pb from 18.65 to 18.92, ɛNd from 8.5 to 3.8, and ɛHf from 13.3 to 8.7. Our data overlap the Sr-Nd-Pb isotopic compositions of primitive samples at Mt. Baker and Chilliwack batholith [4], but extend to more depleted compositions. GVB basalts are isotopically distinct from other Cascade arc primitive basalts, with systematically lower 208Pb/206Pb at a given 206Pb/204Pb and higher ɛNd at a given 87Sr/86Sr. In Pb-Pb space, GVB basalts define a linear trend extending from Explorer MORB to local subducting sediments drilled at ODP Sites 888 and 1027 in the northern Cascadia basin. We interpret this array as a mixing line reflecting variable sediment input to the mantle. However, Sr, Pb and Nd isotope ratios are only weakly correlated with La/Nb and latitude, whereas 208Pb

  13. Factors controlling elevated lead concentrations in water samples from aquifer systems in Florida

    USGS Publications Warehouse

    Katz, B.G.; Bullen, M.P.; Bullen, T.D.; Hansard, Paul

    1999-01-01

    Concentrations of total lead (Pb) and dissolved Pb exceeded the U.S. Environmental Protection Agency action level of 15 micrograms per liter (mg/L) in approximately 19 percent and 1.3 percent, respectively, of ground-water samples collected during 1991-96 from a statewide network of monitoring wells designed to delineate background water quality of Florida's major aquifer systems. Differences in total Pb concentrations among aquifer systems reflect the combined influence of anthropogenic sources and chemical conditions in each system. A highly significant (p<0.001) difference in median total Pb concentrations was found for water samples from wells with water-level recording devices that contain Pb-counterweights (14 mg/L) compared to non-recorder wells (2 mg/L). Differences between total Pb concentrations for recorder and non-recorder wells are even more pronounced when compared for each aquifer system. The largest differences for recorder status are found for the surficial aquifer system, where median total Pb concentrations are 44 and 2.4 mg/L for recorder wells and non-recorder wells, respectively. Leaching of Pb from metal casing materials is another potential source of Pb in ground water samples. Median total Pb concentrations in water samples from the surficial, intermediate, and Floridan aquifer systems are higher from recorder wells cased with black iron than for recorder wells with steel and PVC casing material. Stable isotopes of Pb were used in this study to distinguish between anthropogenic and natural sources of Pb in ground water, as Pb retains the isotopic signature of the source from which it is derived. Based on similarities between slopes and intercepts of trend lines for various sample types (plots of 206Pb/204Pb versus 208Pb/204Pb and 207Pb/204Pb versus 208Pb/204Pb) the predominant source of total Pb in water samples from the surficial aquifer system is corrosion of Pb counterweights. It is likely that only ground-water samples, not the aquifer

  14. Lead-isotopic data from sulfide minerals from the Cascade Range, Oregon and Washington

    USGS Publications Warehouse

    Church, S.E.; LeHuray, A.P.; Grant, A.R.; Delevaux, M.H.; Gray, J.E.

    1986-01-01

    Lead-isotopic studies of mineral deposits associated with Tertiary plutons found in the Cascade Range of Oregon and Washington demonstrate a rather uniform isotopic composition in various sulfide minerals ( 206Pb 204Pb = 18.84 to 19.05; 207Pb 204Pb = 15.57 to 15.62; 208Pb 204Pb = 38.49 to 38.74), show less variation than data from the volcanic rocks of the Cascade Range and fall within the mixing array defined by the MORB regression line and continental sediments. An evaluation of the role of crustal assimilation by hydrothermal convection during emplacement was made on five sulfide deposits associated with a single composite batholith, the Cloudy Pass pluton. The Pb-isotopic data and mass balance calculations suggest that only minor amounts of the lead were derived from the overlying Precambrian (?) Swakane Biotite Gneiss during emplacement. The bulk of the metal that occurs in sulfide deposits in the Cascade mineral belt appears to have been derived from subducted continental detritus. The variation of the Pb-isotopic signature of Sulfides from specific districts or deposits suggests that there is a correlation with age and structure of the crust. 206Pb 204Pb is greater than 18.92 in northern Washington and southern Oregon where deposits have intruded Mesozoic or older crust. However, the ore deposits between the northern Oregon border and central Oregon, south of Eugene, have intruded younger crust composed largely of mafic and andesitic volcanic rocks and 206Pb 204Pb lies between 18.84 and 18.92. This region, previously called the Columbia embayment, appears to be underlain by Tertiary volcanic rocks. Lead-isotopic data may be used to define the boundaries between discontinuous blocks of Mesozoic crust and Tertiary volcanic cover. ?? 1986.

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

    PubMed

    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.

  16. Black Carbon, Metal Concentrations and Lead Isotopes Ratios in Aerosols as Tracers of Human and Natural Activities in Northern Vietnam

    NASA Astrophysics Data System (ADS)

    Guinot, B. P.

    2015-12-01

    Atmospheric brown clouds (ABC) observed as widespread layers of brownish haze are regional scale plumes of air pollutants with a hot spot of emission located in East Asia. ABC are mainly composed of aerosol particles such as Black Carbon (BC) emitted to the atmosphere during biomass burning and fossil fuels combustion. The atmospheric lifetime of BC ranges from a few days in wet season up to one month in dry season. The use of stable lead isotopes and 21 elements as tracers of air pollution was applied to identify and characterized the main sources of anthropogenic activities in Asian region. Aerosol samples from Haiphong (North Vietnam) were collected by a high volume sampler for a period of one year from October 2012 to October 2013. Vietnam's 207Pb/206Pb ratios were almost identical to those found for China. Ratios of 207Pb/206Pb ranged from 0.837 to 0.871 which agrees with values previously reported for the last 10 years in China (0.841 - 0.879). No significant variation in isotope ratio was observed during the sampling period, which suggests that there was no large seasonal variation in the isotope ratios of airborne lead. Trajectory analysis showed that almost two third of the air masses originated from East Northeast which implies that China was a major source of lead in atmosphere. Enrichment factor calculations indicated a large influence of coal activity (EF(Al) As = 1982 ± 796, EF(Al) Cd = 972 ± 659, EF(Al) Sb = 1358 ± 930) but the difference between combustion and mining exploitation could not be evidenced. Significant correlations were found between two others groups of elements: As, Cu, Ni, Zn, and Al, Fe K, Co. Wind dilution was effective on metals concentration variation. During the cold and dry season (winter) ambient concentrations were high and variable, during the warm and wet season (summer) concentrations were stable and low. Taken together, these factors also identified industrial and lithogenic activities in the region.

  17. Revisiting mobilisation of skeletal lead during pregnancy based on monthly sampling and cord/maternal blood lead relationships confirm placental transfer of lead.

    PubMed

    Gulson, Brian; Mizon, Karen; Korsch, Michael; Taylor, Alan

    2016-04-01

    Lead (Pb) can be released from the maternal skeleton during pregnancy and lactation and transferred to the infant. Most support for this hypothesis comes from blood Pb (PbB) studies involving limited sampling during pregnancy, the maximum usually being five samplings, including at delivery. We provide longitudinal data for PbB concentrations and Pb isotopic ratios for three cohorts of pregnant females (n = 31), two of which are based on monthly sampling and the other on quarterly sampling. We also provide data for samples collected post-partum. The data are compared with changes observed in a matched, by country and age, non-pregnant control cohort (n = 5). The monthly data illustrate the variability between subjects, which is also apparent when the data are compared on a trimester basis. Mixed model analyses showed that, in the third trimester, the mean PbB level was significantly lower for women (n = 10) who took a calcium (Ca) supplement (PbB 1.6 µg/dL) than those whose Ca intake was low (low-Ca cohort; n = 15; PbB 2.5 µg/dL) because low Ca means more mobilisation is required for homoeostasis so that more Pb was mobilised from the skeleton. For women who took the supplement, post-partum PbB levels were significantly higher than those in the other periods (2.7 vs 1.4-1.6 µg/dL). For women in the low-Ca cohort, PbB levels were higher at post-partum than in pre-pregnancy and in the first and second trimesters (3.1 vs 1.8 µg/dL), while the levels in the third trimester were higher than those in the first and second trimesters. Importantly, the increase in PbB during gestation was delayed until the third trimester in the Ca-supplemented cohort compared with the low-Ca cohort. Regression analysis showed that the changes over trimester were very similar for PbB and the (206)Pb/(204)Pb ratio providing convincing evidence for extra mobilisation of Pb from the maternal skeleton during pregnancy and lactation. Isotopic ratios in the cord blood samples were similar to

  18. Early Cretaceous low-Mg# adakitic rocks in the southern margin of the central North China Craton: Partial melting of thickened lower continental crust and tectonic implications

    NASA Astrophysics Data System (ADS)

    Yang, D.

    2015-12-01

    This paper reports new whole-rock geochemical, Sr-Nd-Pb isotopic, and zircon U-Pb and Hf isotopic data for Early Cretaceous intrusive rocks in the Sanmenxia-Houma area of central China, and uses these data to constrain the petrogenesis of low-Mg adakitic rocks (LMAR) and the spatial extent of the influence of the deeply subducted Yangtze slab during the Triassic evolution of this region. New zircon LA-ICP-MS U-Pb data indicate that the early- and late-stage southern Quli, Qiligou, and Gaomiao porphyritic quartz diorites, the Canfang granodiorite, and the northern Wangmao porphyritic quartz monzodiorite were emplaced during the Early Cretaceous (~130 Ma) and the late Early Cretaceous (116 Ma). These rocks are characterized by high Na2O/K2O, Sr/Y, and (La/Yb)n ratios as well as high Sr concentrations, low Mg# values, and low heavy rare earth element and Y concentrations, all of which indicate an LMAR affinity. The samples have relatively high initial 87Sr/86Sr ratios (0.7054-0.7095), and low eNd(t) (-11.90 to -22.20) and eHf(t) (-16.7 to -32.7) values, indicative of a lower continental crust origin. The presence of Neoproterozoic (754-542 Ma) and inherited Late Triassic (220 Ma) metamorphic zircons within the late Early Cretaceous LMAR and the relatively high 206Pb/204Pb ratios of these rocks suggest that they formed from primary magmas derived from partial melting of Yangtze Craton (YC) basement material that had undergone ultrahigh-pressure metamorphism. In contrast, the presence of Paleoproterozoic and Archean inherited zircons within early Early Cretaceous LMAR in this area and the relatively low 206Pb/204Pb ratios of these rocks are indicative of derivation from primary magmas generated by partial melting of the thickened lower continental crust of the North China Craton (NCC). These rocks may have formed in an extensional environment associated with the upwelling of asthenospheric mantle material. The presence of YC basement material within the NCC in the

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

    PubMed Central

    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 specialist could be supplemented with routine lead isotope analyses of potential lead sources and blood. Sampling for lead isotopes was undertaken following the U.S. Department of Housing and Urban Development regulatory guidelines for the evaluation of lead hazards in housing, and with the consideration of minimizing the additional costs associated with lead isotope measurements. The range of isotopic ratios within a single residence was large enough to allow the characterization of different lead sources, particularly when both major (e.g., (207)Pb/(206)Pb) and minor (e.g., (206)Pb/(204)Pb) isotope ratios were considered. These cases illustrate the utility of the lead isotope method to identify main source(s) of lead exposure to the child; discard unlikely sources of exposure to the child; point to sources of lead to dust; and substantiate or refine the environmental assessment based exclusively on lead concentrations and loadings. Thus, a more effective evaluation of household lead hazards would likely benefit from considering a) lead concentrations and loadings in and around the household environment; b) all isotopic ratios of potential lead sources within that environment; and c) information about behavioral habits, as well as an evaluation of viable pathways of exposure to the child. PMID:11102302

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

    PubMed

    Gwiazda, R H; Smith, D R

    2000-11-01

    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 specialist could be supplemented with routine lead isotope analyses of potential lead sources and blood. Sampling for lead isotopes was undertaken following the U.S. Department of Housing and Urban Development regulatory guidelines for the evaluation of lead hazards in housing, and with the consideration of minimizing the additional costs associated with lead isotope measurements. The range of isotopic ratios within a single residence was large enough to allow the characterization of different lead sources, particularly when both major (e.g., (207)Pb/(206)Pb) and minor (e.g., (206)Pb/(204)Pb) isotope ratios were considered. These cases illustrate the utility of the lead isotope method to identify main source(s) of lead exposure to the child; discard unlikely sources of exposure to the child; point to sources of lead to dust; and substantiate or refine the environmental assessment based exclusively on lead concentrations and loadings. Thus, a more effective evaluation of household lead hazards would likely benefit from considering a) lead concentrations and loadings in and around the household environment; b) all isotopic ratios of potential lead sources within that environment; and c) information about behavioral habits, as well as an evaluation of viable pathways of exposure to the child.

  1. Geochemistry and age of Shatsky, Hess, and Ojin Rise seamounts: Implications for a connection between the Shatsky and Hess Rises

    NASA Astrophysics Data System (ADS)

    Tejada, Maria Luisa G.; Geldmacher, Jörg; Hauff, Folkmar; Heaton, Daniel; Koppers, Anthony A. P.; Garbe-Schönberg, Dieter; Hoernle, Kaj; Heydolph, Ken; Sager, William W.

    2016-07-01

    Shatsky Rise in the Northwest Pacific is the best example so far of an oceanic plateau with two potential hotspot tracks emanating from it: the linear Papanin volcanic ridge and the seamounts comprising Ojin Rise. Arguably, these hotspot tracks also project toward the direction of Hess Rise, located ∼1200 km away, leading to speculations that the two plateaus are connected. Dredging was conducted on the massifs and seamounts around Shatsky Rise in an effort to understand the relationship between these plateaus and associated seamounts. Here, we present new 40Ar/39Ar ages and trace element and Nd, Pb, and Hf isotopic data for the recovered dredged rocks and new trace elements and isotopic data for a few drill core samples from Hess Rise. Chemically, the samples can be subdivided into plateau basalt-like tholeiites and trachytic to alkalic ocean-island basalt compositions, indicating at least two types of volcanic activity. Tholeiites from the northern Hess Rise (DSDP Site 464) and the trachytes from Toronto Ridge on Shatsky's TAMU massif have isotopic compositions that overlap with those of the drilled Shatsky Rise plateau basalts, suggesting that both Rises formed from the same mantle source. In contrast, trachytes from the southern Hess Rise (DSDP Site 465A) have more radiogenic Pb isotopic ratios that are shifted toward a high time-integrated U/Pb (HIMU-type mantle) composition. The compositions of the dredged seamount samples show two trends relative to Shatsky Rise data: one toward lower 143Nd/144Nd but similar 206Pb/204Pb ratios, the other toward similar 143Nd/144Nd but more radiogenic 206Pb/204Pb ratios. These trends can be attributed to lower degrees of melting either from lower mantle material during hotspot-related transition to plume tail or from less refractory shallow mantle components tapped during intermittent deformation-related volcanism induced by local tectonic extension between and after the main volcanic-edifice building episodes on Shatsky

  2. Resolving mantle and magmatic processes in basalts from the Cameroon volcanic line using the Re-Os isotope system

    NASA Astrophysics Data System (ADS)

    Gannoun, A.; Burton, K. W.; Barfod, D. N.; Schiano, P.; Vlastélic, I.; Halliday, A. N.

    2015-05-01

    This study presents major-, trace element and Re-Os isotope and elemental data for young alkaline basalts (< 10 Ma) from oceanic (Annobon, S. Tomé, Principe), continental (Manengouba) and continent-oceanic boundary (COB, Mt. Cameroon) sectors of the Cameroon volcanic line (CVL). The CVL is a chain of Tertiary to recent, transitional to strongly alkaline intraplate volcanoes extending from the south Atlantic island of Annobon to the continental interior of West Africa (Biu Plateau). The basalts from the oceanic sector display a range of initial 187Os/188Os ratios between 0.128 and 0.190 and those from the COB and continental sector range between 0.142 and 0.560. The samples with high 206Pb/204Pb (e.g. ratios > 20) possess 187Os/188Os isotope compositions between 0.14 and 0.18 (e.g., basalts from Mt Cameroon and Sao Tomé) which reflect the chemical characteristics that are more likely to be primary features of CVL, and are close to the value of 0.153 attributed to the HIMU end-member (Tubuai-Mangaia). However, most of the lavas from the continental sector show highly radiogenic initial 187Os/188Os ratios (0.36 to 0.56) that are outside the range previously observed for ocean island basalts, with shifts to radiogenic Os isotope compositions accompanied by less radiogenic 206Pb/204Pb and increasing SiO2 contents. The increase in 187Os/188Os is also associated with the decrease of Os, Ni, MgO and phenocryst abundances. These data can be explained by fractional crystallisation and assimilation of continental crust by the ascending magma. The systematic shift to unradiogenic lead isotope compositions from the COB into the oceanic sector is positively correlated with variations in 187Os/188Os isotope composition (from 0.140 to 0.128). At first sight this covariation might be attributed to the mixing of HIMU material with the ambient upper mantle (DMM). However, there is a clear covariation of the Os isotope and elemental composition, best explained with contamination of

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

    PubMed

    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

  4. Petrology of continental tholeiitic magmas forming a 350-km-long Mesozoic dyke swarm in NE Brazil: Constraints of geochemical and isotopic data

    NASA Astrophysics Data System (ADS)

    Ngonge, Emmanuel Donald; de Hollanda, Maria Helena Bezerra Maia; Archanjo, Carlos José; de Oliveira, Diógenes Custódio; Vasconcelos, Paulo Marcosde Paula; Muñoz, Patrício Rodrigo Montecinos

    2016-08-01

    The Ceará Mirim dyke swarm (northeastern Brazil) is composed of Cretaceous tholeiites with plagioclase, clinopyroxene (± olivine), Fe-Ti oxides and pigeonite in their groundmass. These tholeiites have been subdivided into three groups: high-Ti olivine tholeiites, evolved high-Ti tholeiites (TiO2 ≥ 1.5 wt.%; Ti/Y > 360), and low-Ti tholeiites (TiO2 ≤ 1.5 wt%; Ti/Y ≤ 360), with all exhibiting distinct degrees of enrichment in incompatible elements relative to Primitive Mantle. Negative Pb anomalies are found in all three groups, while Nb-Ta abundances similar to those of OIB-type magmas are found in the olivine tholeiites, with moderate to high depletions being observed, respectively, in the evolved high-Ti and low-Ti tholeiites. The low-Ti tholeiites exhibit some contamination with crustal (felsic) materials during ascent. The initial isotopic compositions of the olivine tholeiites show uniform and unradiogenic 87Sr/86Sr (~ 0.7035-0.7039) combined with (in part) radiogenic 143Nd/144Nd and 206Pb/204Pb (> 19.1) ratios, which together reveal a likely contribution of FOZO (FOcalZOne) component in their genesis. The other tholeiite groups show variable Sr-Nd ratios with relatively consistent 206Pb/204Pb ratios clustering towards an isotopically enriched mantle (EM1) component. Taken in conjunction with the Nb, this enriched signature reflects the involvement of a subduction-modified lithospheric mantle in the source of the evolved high-Ti and low-Ti tholeiites. Thus, we propose that FOZO and EMI components coexisted (including minor mixing with E-MORB magmas) and contributed in varying extents to the generation of the Ceará-Mirim dyke swarm primary melts, which segregated at 75 to 60 km in depth around the garnet-spinel facies transition zone. The mechanism that promoted melting was most likely non-plume related. We suggest that plate-boundary forces linked to the opening of the Atlantic Ocean promoted passive rifting and that the resulting asthenospheric

  5. U-Pb Dating, whole rock and Sr-Nd-Pb-O isotope geochemistry of collisional magmatism in the CACC: Çiçekdaǧ igneous complex (ÇIC)

    NASA Astrophysics Data System (ADS)

    Deniz, Kiymet; Kagan Kadioglu, Yusuf; Stuart, Finlay; Ellam, Rob; Boyce, Adrian; Condon, Daniel

    2015-04-01

    these intrusive rocks have experienced fractional crystallisation coupled with crustal assimilation. The calcalkaline and alkaline series show enrichment in LILE and LREE relative to HFSE and HREE. These rocks have moderate 208Pb/204Pb (38.87-39.16) and 207Pb/204Pb (15.62-15.71) and high 206Pb/204Pb (18.76-18.81). Both trace element and Pb isotope data indicate enriched mantle source (EM-II). Mafic alkaline rocks differed with their low 206Pb/204Pb (17.55-17.62). These rocks are derived from subduction modified lithospheric mantle. The geochemistry and Sr-Nd-O isotope data of ophiolitic rocks and late alkaline dykes are very similar. Both of them have flat REE pattern, high 87Sr/86Sr and 143Nd/144Nd, low δ18O values (1.9-4.0), moderate 208Pb/204Pb (38.81-38.97, 38.51-38.91) and 207Pb/204Pb (15.62-15.70, 15.54-15.69) and high 206Pb/204Pb (18.37-18.77, 18.39-18.73). All data indicate heterogeneous mantle source. Trace element ratio diagrams suggest depleted mantle source and subduction enrichment for late alkaline dykes. Dy versus Dy/Yb diagram and calculated partial melting curves suggest 20-25% degree of partial melting of amphibole-phlogopite bearing spinel lherzolitic mantle sources. Ba/Rb versus Rb/Sr diagram indicate the presence of amphibole in the mantle source of ophiolitic rocks and phlogopite for the late alkaline dykes. U-Pb dating of zircon yielded crystallization ages of 73.74±0.027-73.78±0.046 and 73.78±0.071 for calcalkaline series and alkaline series, respectively. Both series are coexistence and may have coevally been confined from same sources.

  6. Radiogenic Isotopes in Weathering and Hydrology

    NASA Astrophysics Data System (ADS)

    Blum, J. D.; Erel, Y.

    2003-12-01

    cycling of calcium. The decay of 235U to 207Pb, 238U to 206Pb, and 232Th to 208Pb have half-lives of 0.704 Gyr, 4.47 Gyr, and 14.0 Gyr, respectively, and result in variations in the 207Pb/204Pb, 206Pb/204Pb, and 208Pb/204Pb ratios (e.g., Blum, 1995). Uranium-234 has a half-life of 0.25 Myr and the ratio 234U/238U approaches a constant secular equilibrium value in rocks and minerals if undisturbed for ˜1 Myr. Differences in this ratio are often observed in solutions following rock-water interaction and have been used in studies of weathering and hydrology. Uranium and thorium tend to be highly concentrated in the trace accessory minerals such as zircon, monazite, apatite, and sphene, which therefore develop high 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios. Once released into the hydrosphere, lead retains its isotopic composition without significant geochemical or biological fractionation and tends to generally follow the chemistry of iron in soils and aqueous systems (Erel and Morgan, 1992). The use of the U-Th disequilibrium series as a dating tool falls outside the scope of this chapter and is reviewed in Chapters 6.14 and 6.17 as well as Chapter 3.15. The decay of 147Sm to 143Nd, 176Lu to 176Hf, and 187Re to 187Os have half-lives of 106 Gyr, 35.7 Gyr, and 42.3 Gyr, respectively, and result in natural variability in the 144Nd/143Nd, 176Hf/177Hf, and 187Os/188Os ratios (e.g., Blum, 1995). Neodymium is a rare earth element (REE), hafnium is a transition metal with chemical similarities to zirconium, and osmium is a platinum group element. The geochemical behaviors of these elements in the hydrosphere are largely determined by these chemical affinities.

  7. Geochemical evolution of Monowai volcanic center: New insights into the northern Kermadec arc subduction system, SW Pacific

    NASA Astrophysics Data System (ADS)

    Timm, Christian; Graham, Ian J.; de Ronde, Cornel E. J.; Leybourne, Matthew I.; Woodhead, Jon

    2011-08-01

    We present trace element and Sr-Nd-Pb isotope data on volcanic rocks recovered from the submarine Monowai volcanic center, which marks the midpoint of the ˜2500 km long Tonga-Kermadec arc. The center consists of a large (12 × 9 km) partly hydrothermally active caldera and a 12 km diameter ˜1500 m high volcanically and hydrothermally active stratovolcano. The stratovolcano lavas are tholeiitic basalts, which show variable evidence for plagioclase (±pyroxene) accumulation. The caldera lavas range from basalt to andesite, with the compositional variation being consistent with fractional crystallization as the dominant process. The mafic Monowai magmas were generated by relatively high degrees (12%-20%) of partial melting of a previously depleted MORB-type spinel-peridotitic mantle, metasomatized by slab-derived fluids. Strongly fluid mobile 87Sr/86Sr and 207Pb/204Pb ratios of the Monowai basaltic lavas are similar to those from the Putoto, Raoul, and Macauley volcanic centers 200-400 km to the south, suggesting derivation largely from subducted sediment. In contrast, variably fluid immobile 143Nd/144Nd ratios suggest an isotopically heterogeneous mantle along this segment of the arc. Higher 206Pb/204Pb in Monowai lavas imply some influence from the nearby subducting Louisville seamounts in melt generation. The formation of one of the Earth's largest submarine mafic calderas can best be explained through drainage of a single magma reservoir and subsequent collapse caused by trench-perpendicular extension, probably via southward progressive rifting of the northern Havre Trough.

  8. The Earth's missing lead may not be in the core.

    PubMed

    Lagos, M; Ballhaus, C; Münker, C; Wohlgemuth-Ueberwasser, C; Berndt, J; Kuzmin, Dmitry V

    2008-11-01

    Relative to the CI chondrite class of meteorites (widely thought to be the 'building blocks' of the terrestrial planets), the Earth is depleted in volatile elements. For most elements this depletion is thought to be a solar nebular signature, as chondrites show depletions qualitatively similar to that of the Earth. On the other hand, as lead is a volatile element, some Pb may also have been lost after accretion. The unique (206)Pb/(204)Pb and (207)Pb/(204)Pb ratios of the Earth's mantle suggest that some lead was lost about 50 to 130 Myr after Solar System formation. This has commonly been explained by lead lost via the segregation of a sulphide melt to the Earth's core, which assumes that lead has an affinity towards sulphide. Some models, however, have reconciled the Earth's lead deficit with volatilization. Whichever model is preferred, the broad coincidence of U-Pb model ages with the age of the Moon suggests that lead loss may be related to the Moon-forming impact. Here we report partitioning experiments in metal-sulphide-silicate systems. We show that lead is neither siderophile nor chalcophile enough to explain the high U/Pb ratio of the Earth's mantle as being a result of lead pumping to the core. The Earth may have accreted from initially volatile-depleted material, some lead may have been lost to degassing following the Moon-forming giant impact, or a hidden reservoir exists in the deep mantle with lead isotope compositions complementary to upper-mantle values; it is unlikely though that the missing lead resides in the core.

  9. Nd, Pb and Sr isotopic data from the Mount Elgon volcano, eastern Uganda-western Kenya: Implications for the origin and evolution of nephelinite lavas

    NASA Astrophysics Data System (ADS)

    Simonetti, A.; Bell, K.

    1995-11-01

    Nd, Pb and Sr isotope ratios for nephelinites from the Tertiary Mount Elgon alkaline volcanic centre, eastern Uganda-western Kenya, are highly variable and indicate open system behaviour. The variation in {143Nd }/{144Nd } (0.51219-0.51286) and {87Sr }/{86Sr } (0.70314-0.70604) ratios span almost the entire range documented for carbonatites from several East African alkaline complexes. The whole rock chemical data, mineralogy, composition of diopside phenocrysts, and variation in isotopic ratios from the Mount Elgon nephelinites are similar to those from the nephelinite lavas from the Tertiary Napak volcano, Uganda (Simonetti and Bell, 1994a). The diopside phenocrysts from Mount Elgon nephelinite lavas reveal large core-to-rim compositional variations (which include normal, oscillatory and reverse zoning), and their Nd, Pb and Sr isotopic ratios are not in isotopic equilibrium with their host lavas. Microprobe data along with textural evidence from the Mount Elgon diopside phenocrysts support a model that involves crystallization in an open magma system that was undergoing continuous chemical and isotopic change. The large variation in Pb isotopic ratios (whole rocks- {206Pb }/{204Pb }: 18.45-21.51; {207Pb }/{204Pb }: 15.61-15.88; {208Pb }/{204Pb }: 38.62-41.02), from the Mount Elgon lavas, best fit a model involving mixing between EM I and HIMU mantle components, and correlations in Pb-Sr and Pb-Nd isotopic plots partly support this interpretation. The isotopic data from Mount Elgon and Napak nephelinites suggest complex evolutionary histories involving magma mixing, and support the presence of a heterogeneous sub-continental source beneath eastern Uganda, similar to that documented for various types of peralkaline nephelinite lavas from the only active carbonatite-nephelinite volcano, Oldoinyo Lengai, Tanzania (Bell and Dawson, 1995) and other East African volcanoes (e.g. Vollmer and Norry, 1983). The chemical data and large variation in isotopic ratios for the

  10. B, Sr and Pb isotope geochemistry of high-pressure Alpine metaperidotites monitors fluid-mediated element recycling during serpentinite dehydration in subduction mélange (Cima di Gagnone, Swiss Central Alps)

    NASA Astrophysics Data System (ADS)

    Cannaò, E.; Agostini, S.; Scambelluri, M.; Tonarini, S.; Godard, M.

    2015-08-01

    Tectonic mixing of slab- and mantle-derived materials at the interface between converging plates highly enhances fluid-mediated mass transfer from the slab to the overlying mantle. Subduction mélanges can provide information about the interaction among different slices accreted at plate interface domains, with implications on the tectonic and geochemical evolution of the plate-interface itself. At Cima di Gagnone, pelitic schists and gneiss enclose chlorite harzburgite and garnet peridotite lenses, like in subduction mélanges located in-between downgoing slabs and overlying mantle. These peridotites host MORB-type eclogite and metarodingite, and derive from dehydration of serpentinized mantle protoliths. Their enrichment in fluid-mobile B, As, Sb, U, Th is the result of an early-stage oceanic serpentinization, followed by interaction with host metasediments during subduction burial. Here we define the element exchange process in the Gagnone mélange by means of the B, Sr and Pb isotope analysis of its main lithologies (ultramafic, mafic rocks and paragneiss). The 87Sr/86Sr and 206Pb/204Pb ratios of ultramafic rocks (0.7090-0.7124 and 18.292-18.837, respectively) show enrichments in radiogenic Sr and Pb after exchange with the host paraschist (up to 0.7287 87Sr/86Sr; 18.751 206Pb/204Pb). The δ11B values of peridotites (down to -10‰) point to a combined effect of (1) 11B release to deserpentinization fluids (serpentinized protoliths likely had positive δ11B and lower radiogenic Sr, Pb), and of (2) exchange with fluids from the surrounding metasediments. The whole Gagnone rock-suite is finally overprinted by retrograde fluids that essentially bring to an increase in radiogenic Pb (about 19.0 206Pb/204Pb) and to values of 0.710 87Sr/86Sr and of -10‰ δ11B. The recognition of different stages of interaction between mantle rocks and sedimentary/crustal reservoirs allows us to define the geochemical effects related to the early coupling of such rocks along the

  11. Major, trace element, and isotopic compositions of Vietnamese basalts: Interaction of hydrous EM1-rich asthenosphere with thinned Eurasian lithosphere

    NASA Astrophysics Data System (ADS)

    Nguyen, Hoang; Flower, Martin F. J.; Carlson, Richard W.

    1996-11-01

    Intraplate magmatism affected much of Indochina following the mid-Miocene cessation of South China Sea opening. Thick basalt plateaus formed on accreted terrains of varying age as extensional fractures were reactivated following the Indo-Eurasian collision. The basalts are part of a diffuse igneous province affecting much of eastern and southeastern Asia and western Pacific marginal basins. Most Indochina basalt centers comprise two eruptive episodes, an early (lower) series of high-Si0 2, low-FeO ∗ quartz and olivine tholeiites, tapping a relatively-refractory, lithospheric mantle-type source, and a later (upper) series of low-SiO 2, high-FeO ∗ olivine tholeiites, alkali basalts, and basanites, tapping a fertile, asthenospheric source. This pattern is observed elsewhere in the region (e.g., Hainan Island) and resembles several continental flood basalt provinces. While some crustal contamination is suggested, incompatible trace element and strontium, neodymium, and lead isotopic compositions reflect secular changes from the inferred lithospheric to asthenospheric reservoirs. Lower Series basalts reflect hybrids of 206Pb/204Pb- rich EM2 and N-MORB reservoirs, with high K2O/P 2O5 and low Rb/Sr and Ba/Nb ratios, consistent with the involvement of lithospheric mantle. In contrast, Upper Series basalts show lower K2O/P 2O5 and higher Rb/Sr and Ba/Nb ratios and reflect hybrids of 206Pb/204Pb- poor EM1 and N-MORB sources. These resemble anomalous (A) -MORB compositions that are typical of eastern/southeastern Asian and western Pacific marginal basin asthenosphere. Despite its resemblance to Indian Ocean (I-) MORB, A-MORB "plum-pudding" asthenosphere may be explained in terms of an endogenous Asian model whereby EM1-rich subcratonic lithosphere was entrained by asthenosphere extruded by the Indo-Eurasian collision. This model is consistent with the restriction of diffuse regional magmatism to the late Cenozoic (i.e., following tectonic extrusion), evidence for shallow

  12. Major, trace element, and isotopic compositions of Vietnamese basalts: Interaction of hydrous EM1-rich asthenosphere with thinned Eurasian lithosphere

    NASA Astrophysics Data System (ADS)

    Hoang, Nguyen; Flower, Martin F. J.; Carlson, Richard W.

    1996-11-01

    Intraplate magmatism affected much of Indochina following the mid-Miocene cessation of South China Sea opening. Thick basalt plateaus formed on accreted terrains of varying age as extensional fractures were reactivated following the Indo-Eurasian collision. The basalts are part of a diffuse igneous province affecting much of eastern and southeastern Asia and western Pacific marginal basins. Most Indochina basalt centers comprise two eruptive episodes, an early (lower) series of high-Si0 2, low-FeO * quartz and olivine tholeiites, tapping a relatively-refractory, lithospheric mantle-type source, and a later (upper) series of low-SiO 2, high-FeO * olivine tholeiites, alkali basalts, and basanites, tapping a fertile, asthenospheric source. This pattern is observed elsewhere in the region (e.g., Hainan Island) and resembles several continental flood basalt provinces. While some crustal contamination is suggested, incompatible trace element and strontium, neodymium, and lead isotopic compositions reflect secular changes from the inferred lithospheric to asthenospheric reservoirs. Lower Series basalts reflect hybrids of 206Pb/ 204Pb-rich EM2 and N-MORB reservoirs, with high K 2O/P 2O 5 and low Rb/Sr and Ba/Nb ratios, consistent with the involvement of lithospheric mantle. In contrast, Upper Series basalts show lower K 2O/P 2O 5 and higher Rb/Sr and Ba/Nb ratios and reflect hybrids of 206Pb/ 204Pb-poor EM1 and N-MORB sources. These resemble anomalous (A) -MORB compositions that are typical of eastern/southeastern Asian and western Pacific marginal basin asthenosphere. Despite its resemblance to Indian Ocean (I-) MORB, A-MORB “plum-pudding” asthenosphere may be explained in terms of an endogenous Asian model whereby EM1-rich subcratonic lithosphere was entrained by asthenosphere extruded by the Indo-Eurasian collision. This model is consistent with the restriction of diffuse regional magmatism to the late Cenozoic (i.e., following tectonic extrusion), evidence for

  13. Does a Superswell Exist Between Antarctica and Australia?

    NASA Astrophysics Data System (ADS)

    Park, S. H.; Langmuir, C. H.; Scott, S. R.; Sims, K. W. W.; Lin, J.; Kim, S.; Michael, P. J.; Hahm, D.

    2015-12-01

    The Australian-Antarctic Ridge (AAR) is located between the Australian-Antarctic Discordance (AAD) of the Southeast Indian ridge (SEIR) in the west and Pacific-Antarctic Ridge (PAR) in the east. The AAR has intermediate spreading rate (~70 mm/yr) and consists of a series of 1st order segments bounded by parallel transform faults. KR1, a southernmost segment (63°S) of the AAR, is a 300-km-long super-segment with shallow axial depth (~2000 m). KR1 is bounded by the Macquarie transform fault in the east and the Balleney transform fault in the west, which connects KR1 with KR2 at ~ 200 km north. KR2 is 180 km long with axial depth (~2300 m) deeper than KR1. Both KR1 and KR2 are shallow relative to global mid-ocean ridges. Most of the basaltic rocks from the two segments show enriched geochemical characteristics that differ from both the AAD (Southeast Indian Ridge) and the PAR. La/Sm ratios vary from N-MORB to T-MORB; however, K2O/Nb ratios of all samples are consistently low like OIB. Their Pb isotopes are mostly more radiogenic than the N-MORB samples from PAR (and EPR) and SEIR, with 206Pb/204Pb mostly >18.6. At a given 206Pb/204Pb, their 87Sr/86Sr are higher than the PAR, but lower than the SEIR. The basalts from the two segments are geochemically similar to Cenozoic volcanoes erupted on southeast Australia, Zealandia and northwest Antarctica, suggesting a genetic relationship. According to tectonic reconstruction models, these three continents were originally joined, but separated from each other after ~80 Ma. Notably, the KR1 and KR2 segments are located at the boundary of this continental separation. The ages of Cenozoic volcanoes span from ~ 60 Ma to the recent, and the volcanoes might be related to a plume head that caused the breakup of the continents. Seismic tomography studies show that there is a low velocity zone (LVZ) in the shallow mantle (> 250 km) between Antarctica and Australia where the AAR is located. The AAR would be sampling this LVZ, and this

  14. Investigating Compositional Links Between Arc Magmas And The Subducted Altered Oceanic Crust

    NASA Astrophysics Data System (ADS)

    Straub, S. M.

    2015-12-01

    Arc magmatism is causally related to the recycling of materials from the subducting plate. Numerous studies showed that the recycled material flux is dominated by recycled continental crust (oceanic sediment, eroded crust) and altered oceanic igneous crust (AOC). The crustal component is highly enriched, and thus its signal in arc magmas can readily be distinguished from mantle wedge contributions. In contrast, the impact of the AOC flux is much more difficult to detect, since the AOC isotopically resembles the mantle. Mass balance studies of arc input and output suggest that the recycled flux from the thick (6000 meter on average) AOC may buffer the flux of the recycled continental crust to the point of concealment in arc settings where the latter is volumetrically minor. In particular, highly fluid- mobile elements Sr and Pb in arc magmas are strongly influenced by the AOC, implying that the arc chemistry may allow for inferring the Sr and Pb isotopic composition of the subducted AOC. This hypothesis is being tested by a compilation of published data of high-quality trace element and isotope compositions from global arcs. In agreement with previous studies, our results confirm that the Sr-rich fluids released from the AOC control the arc Sr isotopes, whereby the slightly elevated 87Sr/86Sr (up to 0.705) of many arcs may principally reflect the similarly elevated Sr isotope ratios of the AOC rather than a recycled crustal component. In contrast, the arc Pb isotope ratios are influenced by both the AOC and the recycled crustal component which create the typical binary mixing arrays. These arrays should then point to the Pb isotope composition of the AOC and the recycled crust, respectively. However, as the proportions of these end members may strongly vary in arc magmas, the exact 206Pb/204Pb of the subducted AOC in a given setting is challenging. Remarkably, the Pb isotope systematics from well-constrained western Aleutian (minimal sediment subduction) and central

  15. The Eldivan ophiolite and volcanic rocks in the İzmir-Ankara-Erzincan suture zone, Northern Turkey: Geochronology, whole-rock geochemical and Nd-Sr-Pb isotope characteristics

    NASA Astrophysics Data System (ADS)

    Çelik, Ömer Faruk; Chiaradia, Massimo; Marzoli, Andrea; Billor, Zeki; Marschik, Robert

    2013-07-01

    Gabbros and dolerite dikes of the Eldivan ophiolite and basaltic volcanic rocks of the ophiolitic mélange in the central part of the İzmir-Ankara-Erzincan (IAE) suture zone were investigated for their 40Ar/39Ar age and whole-rock-major-trace element and Sr-Nd-Pb isotope compositions. Based on geological and geochemical characteristics basaltic volcanic rocks in the ophiolitic mélange are subdivided into two groups (Groups I and II) with ocean island basalts or enriched mid-ocean ridge basalt characteristics, respectively. Gabbros and dolerite dikes of the Eldivan ophiolite (Groups III and IV) have instead geochemical compositions indicative of a subduction-related environment. The volcanic rocks of Group I have 87Sr/86Sr(i) between 0.7037 and 0.7044, ƐNd(i)-DM of - 4.5 to - 5.6, and 206Pb/204Pb(i) ranging between 18.35 and 18.75. Group II volcanic rocks have higher 87Sr/86Sr(i) values (0.7049-0.7055), ƐNd(i)-DM ranging between - 5.4 and - 6.0, and 206Pb/204Pb(i) between 18.14 and 18.62. The Nd isotopic signatures and 207Pb/204Pb(i) values of the volcanic rocks of both groups point to a different source with respect to those of the Eldivan ophiolite. The low 206Pb/204Pb(i) values relative to the ophiolitic rocks seem to exclude a significant contribution from a HIMU reservoir, whereas the 207Pb/204Pb(i) values slightly above the NHRL might indicate some contribution from an EM2-type reservoir. Gabbros (Group III) of the Eldivan ophiolite and dolerite dikes (Group IV) cross-cutting the ultramafic part of the ophiolite show 87Sr/86Sr(i) between 0.7038 and 0.7053, ƐNd(i)-DM from - 2 to - 3.6 and 206Pb/204Pb(i) between 18.10 and 18.80. The gabbros yield ca. 150 Ma 40Ar/39Ar amphibole-plateau ages, which, together with the geochemical data, indicate that they were produced above subducted oceanic lithosphere in the IAE ocean domain in Late Jurassic times. Therefore, the Eldivan ophiolite in the IAE suture zone constitutes a link between the Hellenide

  16. Lower-crustal xenoliths from Jurassic kimberlite diatremes, upper Michigan (USA): Evidence for Proterozoic orogenesis and plume magmatism in the lower crust of the southern Superior Province

    USGS Publications Warehouse

    Zartman, Robert E.; Kempton, Pamela D.; Paces, James B.; Downes, Hilary; Williams, Ian S.; Dobosi, Gábor; Futa, Kiyoto

    2013-01-01

    Jurassic kimberlites in the southern Superior Province in northern Michigan contain a variety of possible lower-crustal xenoliths, including mafic garnet granulites, rare garnet-free granulites, amphibolites and eclogites. Whole-rock major-element data for the granulites suggest affinities with tholeiitic basalts. P–T estimates for granulites indicate peak temperatures of 690–730°C and pressures of 9–12 kbar, consistent with seismic estimates of crustal thickness in the region. The granulites can be divided into two groups based on trace-element characteristics. Group 1 granulites have trace-element signatures similar to average Archean lower crust; they are light rare earth element (LREE)-enriched, with high La/Nb ratios and positive Pb anomalies. Most plot to the left of the geochron on a 206Pb/€204Pb vs 207Pb/€204Pb diagram, and there was probably widespread incorporation of Proterozoic to Archean components into the magmatic protoliths of these rocks. Although the age of the Group 1 granulites is not well constrained, their protoliths appear to be have been emplaced during the Mesoproterozoic and to be older than those for Group 2 granulites. Group 2 granulites are also LREE-enriched, but have strong positive Nb and Ta anomalies and low La/Nb ratios, suggesting intraplate magmatic affinities. They have trace-element characteristics similar to those of some Mid-Continent Rift (Keweenawan) basalts. They yield a Sm–Nd whole-rock errorchron age of 1046 ± 140 Ma, similar to that of Mid-Continent Rift plume magmatism. These granulites have unusually radiogenic Pb isotope compositions that plot above the 207Pb/€204Pb vs 206Pb/€204Pb growth curve and to the right of the 4·55 Ga geochron, and closely resemble the Pb isotope array defined by Mid-Continent Rift basalts. These Pb isotope data indicate that ancient continental lower crust is not uniformly depleted in U (and Th) relative to Pb. One granulite xenolith, S69-5, contains quartz, and has a

  17. Age and Geochemistry of Central American Forearc Basement Rocks (DSDP Leg 67 and 84) Reveal a Complex Geodynamic History

    NASA Astrophysics Data System (ADS)

    Geldmacher, J.; Hoernle, K. A.; Hauff, F.; Kluegel, A.; Bogaard, P. V.

    2006-12-01

    The wide shelf between Costa Rica and southern Mexico hosts an unusually broad forearc basin. Geophysical investigations imply that the entire forearc basement is composed of ophiolitic rocks similar to exposed terranes of the widespread Caribbean Large Igneous Province (CLIP). Various geodynamic models have been suggested for the origin of the CLIP including its formation above the Galápagos plume head. Besides it's origin, the spatial extent and duration of CLIP volcanism are controversial. During DSDP Leg 67 and 84 the forearc basement was drilled and various igneous rocks including basalts, dolerites, gabbros and serpentinized peridotites were recovered. We present 40Ar/39Ar laser age and geochemical data (including major- and trace elements and Sr, Nd, Pb and Hf isotope ratios) of the drilled samples in order to determine if the igneous forearc basement represents old Pacific ocean crust, ancient arc volcanism, and/or accreted intraplate volcanic rocks possibly related to the CLIP? The igneous forearc basement can be subdivided into two groups: a geochemically strongly depleted group and an underlying geochemically enriched group. Mafic rocks of the depleted group have tholeiitic to basaltic andesitic compositions and display a strong depletion in incompatible elements but distinct enrichments of fluid-mobile elements such as Rb, Ba, U, K, Pb and Sr characteristic of arc volcanism. In contrast, alkali basaltic to hawaiitic rocks of the enriched group exhibit enriched incompatible element signatures with marked depletions in K, Pb and heavy rare earth elements similar to Ocean Island Basalt (OIB). Consistent with the trace element division, both groups form two separate fields in Sr, Nd, Pb, and Hf isotopic space with the depleted group showing isotopically depleted initial compositions (low 206Pb/204Pb=17.93-18.48 and 207Pb/204Pb=15.49-15.53 but elevated ^{143}Nd/^{144}Nd= 0.51294-0.51318 and ^{176}Hf/^{177}Hf= 0.28304-0.28316) and the enriched group having

  18. Lead Isotopes from the Upper Mississippi Valley District: A Regional Perspective

    USGS Publications Warehouse

    Millen, Timothy M.; Zartman, Robert E.; Heyl, Allen Van

    1995-01-01

    New lead isotopic data on galena from within and peripheral to the Upper Mississippi Valley lead-zinc district make it possible, by extending coverage to outlying locations, to trace the pathway traversed by the mineralizing fluids beyond the boundary of the main district. All but one of the samples exhibit elevated ratios of the radiogenic isotopes typical of the Upper Mississippi Valley ore deposits; 206PbP04Pb ranges from 19.38 to 24.46, 207PbP04Pb ranges from 15.73 to 16.24, and 208PbP04Pb ranges from 39.24 to 43.69. Galena from the Pints quarry near Waterloo, Iowa, has distinctly lower values of these ratios and may not be related paragenetically to the other samples. Otherwise, the lowest ratios are for samples in the southern part of the region in north-central Illinois, and the highest ratios are for samples to the northeast of the main district in the vicinity of Madison, Wisconsin. Thus, an isotopic pattern rather similar to that observed originally by Heyl and others (1966) prevails regionally, although the predominant fluid flow is now believed to have emanated from the Illinois Basin rather than from the Forest City Basin. Metal-bearing brines being driven northward out of the Illinois Basin probably played the key role in mineralization of the Upper Mississippi Valley district. Both the new and the previously reported lead ratios for the Upper Mississippi Valley district are plotted on 207PbP04Pb and Pb208/pb204Pb versus 206PbP04Pb diagrams, which permit their comparison and the calculation of refined slopes for the expanded data set. A two-stage model age for the time of mineralization can be determined from the 207PbP04Pb_Pb206/Pb204 slope, provided that the source age of the lead is known. With our limited know ledge of this source age, the time of mineralization cannot be tightly constrained but is permissive of a Permian or younger lateral secretion event, as suggested by other geochronological results.

  19. Asthenosphere versus lithosphere as possible sources for basaltic magmas erupted during formation of the Red Sea: constraints from Sr, Pb and Nd isotopes

    NASA Astrophysics Data System (ADS)

    Altherr, Rainer; Henjes-Kunst, Friedhelm; Baumann, Albrecht

    1990-01-01

    Representative basalts from the axial trough of the Red Sea and from volcanic fields of the Arabian Peninsula ranging in composition from N-type MORB to basanite and in age from Early Miocene to Recent show a limited variation in their isotopic compositions: 87Sr/ 86Sr= 0.70240-0.70361 , 206Pb/ 204Pb= 18.040-19.634 , 207Pb/ 204Pb= 15.496-15.666 , 208Pb/ 204Pb= 37.808-39.710 , 143Nd/ 144Nd= 0.513194-0.512670 . There is a poorly constrained correlation between chemical composition and isotope ratios: with increasing alkalinity, Sr and Pb isotope ratios increase and the Nd isotope ratio tends to decrease. In Pb isotope variation diagrams most of the basalts plot significantly above the NHRLs, irrespective of tectonic setting, i.e. thickness of underlying crust and/or lithosphere. MORBs from the axial trough of the Red Sea have higher Pb isotope ratios for a given 87Sr/ 86Sr than MORBs from the Indian Ocean ridges, including the Carlsberg Ridge. It is therefore suggested that both spreading ridges tap different convective systems in the asthenosphere. The tectonic setting of the basalts is reflected in their Nd sbnd Sr isotope characteristics. Basalts from areas where the continental lithosphere is drastically thinned or absent (i.e. Red Sea axial trough and coastal plain, Afar) plot along a reference line defined by N-type MORB and Tristan da Cunha. Basalts erupted in areas with Pan-African crust of normal thickness and moderately thinned lithospheric mantle (i.e. rift shoulder) are characterized by relative low 143Nd/ 144Nd ratios and plot below the reference line towards an EM I component which is also found in the subcontinental lithospheric mantle. These differences in the Nd sbnd Sr isotopic compositions of the basalts are independent of bulk-rock chemistry and are therefore controlled by tectonic setting alone. It is suggested that the low- 143Nd/ 144Nd trend of basalts from the Arabian rift shoulder is caused by a significant contribution of the pre

  20. Zircon U-Pb dating, geochemistry and Sr-Nd-Pb-Hf isotopes of the Wajilitag alkali mafic dikes, and associated diorite and syenitic rocks: Implications for magmatic evolution of the Tarim large igneous province

    NASA Astrophysics Data System (ADS)

    Zou, Si-Yuan; Li, Zi-Long; Song, Biao; Ernst, Richard E.; Li, Yin-Qi; Ren, Zhong-Yuan; Yang, Shu-Feng; Chen, Han-Lin; Xu, Yi-Gang; Song, Xie-Yan

    2015-01-01

    The Early Permian Tarim large igneous province (Tarim LIP) consists mainly of basaltic lavas, mafic-ultramafic intrusions including dikes and, syenite bodies in the Tarim Basin, NW China. A major unit of the Tarim LIP, the Wajilitag intrusive complex, consists of olivine pyroxenite, clinopyroxenite and gabbro units (from bottom to top), diorite and syenite rocks occurred in the upper part of the complex and alkali mafic dikes intrude the clinopyroxenite phase. Here we report the zircon U-Pb age and Hf isotopes, geochemical characteristics and Sr-Nd-Pb isotopic data of the alkali mafic dikes, and diorite, aegirine-nepheline syenite and syenite porphyry units in the Wajilitag intrusive complex. Zircons from the diorite and alkali mafic rocks yield concordant crystallization ages of 275.2 ± 1.2 Ma and 281.4 ± 1.7 Ma, respectively. The diorite and syenitic rocks in Wajilitag area have a narrow range of SiO2 contents (51.9-57.3 wt.%), and are enriched in total alkalis (Na2O + K2O = 8.3-14.3 wt.%), among which the aegirine-nepheline syenite and syenite porphyry have the geochemical affinity of A-type granites. The alkali mafic rocks and syenitic rocks have high Al2O3 (19.4-21.1 wt.%), Zr, Hf, Ba contents, total rare earth element abundances and LREE/HREE ratios and low Mg# value, K, P and Ti contents. Diorites have lower Al2O3 contents, total REE abundances and LREE/HREE ratios and higher Mg# values than the alkali mafic rocks and syenitic rocks. The diorites and syenitic rocks have low initial 87Sr/86Sr ratios (0.7034-0.7046), and high εNd(t) values (0.1-4.1) and zircon εHf(t) values (- 0.9-4.4). All the diorites and syenitic rocks show the 206Pb/204Pb ratios ranging of 18.0-19.5, 207Pb/204Pb of 15.4-15.6 and 208Pb/204Pb of 38.0-39.9. Sr-Nd isotopic ratios indicate a FOZO-like mantle source for the diorite and syenitic rocks, similar to that of the mafic-ultramafic rocks in the Wajilitag complex. In contrast, zircon Hf isotopes of basalt and syenite elsewhere in the

  1. New insights into the petrogenesis of volcanic rocks in the Shanghang Basin in the Fujian Province, China

    NASA Astrophysics Data System (ADS)

    Jiang, Si-Hong; Bagas, Leon; Liang, Qing-Ling

    2015-06-01

    The Mesozoic Shanghang Basin in southeastern China consists of Early Cretaceous mottled coarse-grained clastic and volcanic rocks, and Late Cretaceous clastic rocks. The volcanic rocks are intermediate-mafic to felsic and spatially close to the famous Zijinshan Mineral Field. In order to better understand the timing, petrogenesis and tectonic setting of these volcanic rocks and the relationship between magmatism and metallogeny in the mineral field, U-Pb zircon geochronological, geochemical and Sr-Nd-Pb-Hf isotopic studies were completed on the volcanic rocks. Fifteen LA-MC-ICP-MS U-Pb zircon analyses of the volcanic rocks yield weighted mean ages of between 105 and 99 Ma. Major and trace element geochemistry shows that these rocks are mostly high-K to shoshonitic, enriched in LREE and Th, U, and depleted in Ba, Nb, Sr, P and Ti. The volcanic rocks have 87Sr/86Sri ratios of between 0.70732 and 0.70977, 206Pb/204Pb isotope ratios of 18.57-19.77, 207Pb/204Pb isotope ratios of 15.64-15.71, 208Pb/204Pb isotope ratios of 38.87-40.62, 176Hf/177Hf ratios of 0.282589-0.282823, εNdT values of -7.5 to -4.7, and εHf(t) values of -4.2 to 4. Such characteristics, with similarities to coeval volcanic and intrusive rocks adjacent to the basin, suggest that the parent magma of the Cretaceous volcanic rocks in the basin and their contemporaneous intrusives originated from crustal melts with a juvenile component. Petrogenetically, fractional crystallization with minor wall-rock assimilation is the controlling process in deriving a wide range of more evolved rocks. With reference to the ore-forming events and isotopic features of ore-related intrusions in the Zijinshan Mineral Field, we propose that volcanism in the Shanghang Basin and coeval magmatism in the mineral field are related to the formation of the regional porphyry and epithermal Cu-Au-Mo-Ag deposits in an extension tectonic setting related to the subduction of the Paleo-Pacific Plate.

  2. Zircon U-Pb ages, geochemical and Sr-Nd-Pb-Hf isotopic constraints on petrogenesis of the Tarom-Olya pluton, Alborz magmatic belt, NW Iran

    NASA Astrophysics Data System (ADS)

    Nabatian, Ghasem; Jiang, Shao-Yong; Honarmand, Maryam; Neubauer, Franz

    2016-02-01

    A petrological, geochemical and Sr-Nd-Pb isotopic study was carried out on the Tarom-Olya pluton, Iran, in the central part of the Alpine-Himalayan orogenic belt. The pluton is composed of diorite, monzonite, quartz-monzonite and monzogranite, which form part of the Western Alborz magmatic belt. LA-ICP-MS analyses of zircons yield ages from 35.7 ± 0.8 Ma to 37.7 ± 0.5 Ma, interpreted as the ages of crystallization of magmas. Rocks from the pluton have SiO2 contents ranging from 57.0 to 69.9 wt.%, high K2O + Na2O (5.5 to 10.3 wt.%) and K2O/Na2O ratio of 0.9 to 2.0. Geochemical discrimination criteria show I-type and shoshonitic features for the studied rocks. All investigated rocks are enriched in light rare earth elements (LREEs), large ion lithophile elements (LILEs), depleted in high-field strength elements (HFSEs), and show weak or insignificant Eu anomalies (Eu/Eu* = 0.57-1.02) in chondrite-normalized trace element patterns. The Tarom-Olya pluton samples also show depletions in Nb, Ta and Ti typical of subduction-related arc magmatic signatures. The samples have relatively low ISr (0.7047-0.7051) and positive εNd(36 Ma) (+ 0.39 to + 2.10) values. The Pb isotopic ratios show a (206Pb/204Pb)i ratio of 18.49-18.67, (207Pb/204Pb)i ratio of 15.58-15.61 and (208Pb/204Pb)i ratio of 38.33-38.77. The εHf(t) values of the Tarom-Olya pluton zircons vary from - 5.9 to + 8.4, with a peak at + 2 to + 4. The depleted mantle Hf model ages for the Tarom-Olya samples are close to 600 Ma. These isotope evidences indicate contribution of juvenile sources in petrogenesis of the Tarom-Olya pluton. Geochemical and isotopic data suggest that the parental magma of the Tarom-Olya pluton was mainly derived from a sub-continental lithospheric mantle source, which was metasomatized by fluids and melts from the subducted Neotethyan slab with a minor crustal contribution. Subsequent hot asthenospheric upwelling and lithospheric extension caused decompression melting in the final stage of

  3. Late Jurassic sodium-rich adakitic intrusive rocks in the southern Qiangtang terrane, central Tibet, and their implications for the Bangong-Nujiang Ocean subduction

    NASA Astrophysics Data System (ADS)

    Li, Yalin; He, Juan; Han, Zhongpeng; Wang, Chengshan; Ma, Pengfei; Zhou, Aorigele; Liu, Sheng-Ao; Xu, Ming

    2016-02-01

    The lack of magmatic records with high-quality geochronological and geochemical data in the central segment of the southern Qiangtang subterrane in central Tibet inhibits a complete understanding of the subduction polarity of the Bangong-Nujiang Ocean lithosphere during the Mesozoic. In this study, we present the zircon U-Pb age as well as geochemical and Sr-Nd-Pb isotopic data for the Late Jurassic pluton from the Kangqiong area in the central segment of the southern Qiangtang subterrane. The Kangqiong pluton primarily consists of granodiorites (SiO2 = 62.87-65.17 wt.%) and was emplaced in the Late Jurassic (147.6 ± 2.4-149.9 ± 2.1 Ma). The granodiorites display high Na2O numbers (Na2O/K2O = 1.75-2.24) as well as high MgO (2.21-3.14 wt.%) and Mg-numbers (53-58), are characterized by a low abundance of heavy rare earth elements (e.g., Yb = 1.05-1.92 ppm) and Y (12.63-17.52 ppm), and high Sr/Y (29-61) and La/Yb (14-18) ratios, which are comparable in composition to those of slab-derived adakitic rocks. The Kangqiong adakitic granodiorites have initial (87Sr/86Sr)i ratios of 0.70611 to 0.70669, negative εNd(t) values (- 1.06 to - 0.25), (206Pb/204Pb)t ratios of 18.42 to 18.47, (207Pb/204Pb)t ratios of 15.62 to 15.63, and (208Pb/204Pb)t ratios of 38.50 to 38.60. These geochemical signatures indicate that the magmas were most likely derived from the partial melting of the subducted Bangong-Nujiang oceanic crust and minor contaminants from the accretionary complex. Our results, in combination with the coeval magmatism in the western segment of the southern Qiangtang subterrane, indicate that the Bangong-Nujiang oceanic lithosphere was subducted northward beneath the Qiangtang Terrane, forming a west-east magmatic arc over 800 km during the Late Jurassic.

  4. Lead and barium sources in Cambrian siliciclastics and sediment provenance of a sector of the Taconic Orogen, Quebec: a mixing scenario based on Pb-isotopic evidence

    USGS Publications Warehouse

    Schrijver, K.; Zartman, R.E.; Williams-Jones, A. E.

    1994-01-01

    To test the hypothesis that siliciclastic rocks constituted the major source of Pb and Ba in barite-galena deposits of the Taconic Orogen, we determined Pb-isotope ratios in galena, barren rocks and contained minerals, as well as concentrations of Pb, U, Th and Ba in the latter (detrital feldspars, sandstones, mudstones, rock clasts and carbonate cements and clasts). Ranges in 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb of 28 galena samples are 17.96-18.05, 15.56-15.59 and 37.75-37.93, respectively; ranges for 41 barren rocks and minerals are 16.17-23.31, 15.26-15.86 and 35.98-42.51, respectively. The lowest ratios are in feldspar, and the highest in carbonate and mudstone. Values of the mudstones samples overlap those of galena when corrected for in situ decay of U and Th since galena precipitation (???450 Ma). We thus propose that mudstones constituted a source of lead. Corrected ratios for anomalously Pb-rich mudstones are virtually identical to galena-Pb ratios and may be due to contamination by lead-bearing brines. Assuming that burial diagenesis did not disturb the Pb-isotope values of sandstones, these rocks contributed only a minor fraction of lead to the galena, estimated at ???20% for one deposit. The source of barite-Ba was probably perthite. Low Ba and Pb concentrations of sandstone adjacent to this deposit, compared to high concentrations remote from it, support leaching of barium (and minor lead) from feldspar penecontemporaneous with feldspar dissolution. Geological data indicate that the provenance of the siliciclastic rocks was mainly from Grenville terrane. A comparison of our Pb-isotopic data for Taconic perthite with those of Grenville K-feldspar, as well as ratios of trace elements, support this provenance for both sandstones and mudstones. The presence of carbonate platforms peripheral to the orogen, and the Middle Ordovician-Middle Devonian depositional range of the studied and Mississippi Valley type deposits north (Newfoundland) and south (U

  5. Ancient recycled crust beneath the Ontong Java Plateau: Isotopic evidence from the garnet clinopyroxenite xenoliths, Malaita, Solomon Islands

    NASA Astrophysics Data System (ADS)

    Ishikawa, Akira; Kuritani, Takeshi; Makishima, Akio; Nakamura, Eizo

    2007-07-01

    We present a Sr, Nd, Hf and Pb isotope investigation of a set of garnet clinopyroxenite xenoliths from Malaita, Solomon Islands in order to constrain crustal recycling in the Pacific mantle. Geological, thermobarometric and petrochemical evidence from previous studies strongly support an origin as a series of high-pressure (> 3 GPa) melting residues of basaltic material incorporated in peridotite, which was derived from Pacific convective mantle related to the Ontong Java Plateau magmatism. The present study reveals isotopic variations in the pyroxenites that are best explained by different extents of chemical reaction with ambient peridotite in the context of a melting of composite source mantle. Isotopic compositions of bimineralic garnet clinopyroxenites affected by ambient peridotite fall within the oceanic basalt array, similar to those of Ontong Java Plateau lavas. In contrast, a quartz-garnet clinopyroxenite, whose major element compositions remain intact, has lower 206Pb/ 204Pb- 143Nd/ 144Nd and higher 87Sr/ 86Sr- 207Pb/ 204Pb ratios than most oceanic basalts. These isotopic signatures show some affinity with proposed recycled sources such as the so-called EM-1 or DUPAL types. Constraints from major and trace element characteristics of the quartz-garnet clinopyroxenite, the large extent of Hf-Nd isotopic decoupling and the good coincidence of Pb isotopes to the Stacey-Kramers curve, all indicate that pollution of southern Pacific mantle occurred by the subduction or delamination of Neoproterozoic granulitic lower crust (0.5-1 Ga). This crustal recycling could have taken place around the suture of Rodinia supercontinent, a part of which resurfaced during mantle upwelling responsible for creating the Cretaceous Ontong Java Plateau.

  6. Constraints on mantle source and interactions from He-Sr isotope variation in Italian Plio-Quaternary volcanism

    NASA Astrophysics Data System (ADS)

    Martelli, M.; Nuccio, P. M.; Stuart, F. M.; di Liberto, V.; Ellam, R. M.

    2008-02-01

    Helium isotope ratios of olivine and pyroxene phenocrysts from Plio-Quaternary volcanic rocks from southern Italy (seven Aeolian Islands, Mt. Vulture, Etna, Ustica, and Pantelleria) range from 2.3 to 7.1 Ra. Importantly, the phenocryst 3He/4He correlate well with whole rock Sr isotopic composition (0.70309-0.70711), reflecting the mixing of two sources. A significant contribution of He from crustal contamination is recorded only occasionally (e.g., pyroxenes from Vulcano). When merged with data from the Roman Comagmatic Province, a remarkably strong near-linear He-Sr isotope correlation is apparent. The general northward decrease in 3He/4He corresponds to an increase in 87Sr/86Sr (and a decrease in 143Nd/144Nd and 206Pb/204Pb) that is due to increasing metasomatic enrichment of the mantle wedge via subduction of the Ionian-Adriatic plate. Calculations based on the ingrowth of 4He in the wedge and on the 4He content of the subducting crust show that mechanisms of enrichment in radiogenic He are effective only if the wedge is strongly depleted in He relative to best estimates of the depleted mantle. This can be accommodated if the process of metasomatism by the subduction fluids depletes the mantle wedge. The 3He/4He of Pantelleria, Etna, Iblei, Ustica, Alicudi, and Filicudi basalts (7.0 ± 0.6 Ra) define the mantle composition least affected by subduction-related metasomatism. Although these volcanoes are from a variety of tectonic regimes (subduction-related, intraplate, rifting), their similarities suggest a common origin of geochemical features. Their characteristics are consistent with a HIMU-type mantle that either is younger than the Cook-Austral island end-member or has a lower 238U/204Pb.

  7. Surface dust wipes are the best predictors of blood leads in young children with elevated blood lead levels

    SciTech Connect

    Gulson, Brian; Anderson, Phil; Taylor, Alan

    2013-10-15

    Background: As part of the only national survey of lead in Australian children, which was undertaken in 1996, lead isotopic and lead concentration measurements were obtained from children from 24 dwellings whose blood lead levels were ≥15 µg/dL in an attempt to determine the source(s) of their elevated blood lead. Comparisons were made with data for six children with lower blood lead levels (<10 µg/dL). Methods: Thermal ionisation and isotope dilution mass spectrometry were used to determine high precision lead isotopic ratios ({sup 208}Pb/{sup 206}Pb, {sup 207}Pb/{sup 206}Pb and {sup 206}Pb/{sup 204}Pb) and lead concentrations in blood, dust from floor wipes, soil, drinking water and paint (where available). Evaluation of associations between blood and the environmental samples was based on the analysis of individual cases, and Pearson correlations and multiple regression analyses based on the whole dataset. Results and discussion: The correlations showed an association for isotopic ratios in blood and wipes (r=0.52, 95% CI 0.19–0.74), blood and soil (r=0.33, 95% CI −0.05–0.62), and blood and paint (r=0.56, 95% CI 0.09–0.83). The regression analyses indicated that the only statistically significant relationship for blood isotopic ratios was with dust wipes (B=0.65, 95% CI 0.35–0.95); there were no significant associations for lead concentrations in blood and environmental samples. There is a strong isotopic correlation of soils and house dust (r=0.53, 95% CI 0.20–0.75) indicative of a common source(s) for lead in soil and house dust. In contrast, as with the regression analyses, no such association is present for bulk lead concentrations (r=−0.003, 95% CI −0.37–0.36), the most common approach employed in source investigations. In evaluation of the isotopic results on a case by case basis, the strongest associations were for dust wipes and blood. -- Highlights: • Children with elevated blood lead ≥15 µg/dL compared with a group with <10

  8. Mantle Source of Cretaceous Seafloor in the Nova-Canton Trough

    NASA Astrophysics Data System (ADS)

    Pyle, D. G.; Mahoney, J. J.

    2006-12-01

    The Nova-Canton Trough (NCT) is an 8-km-deep abyss that merges with the far western trace of the Clipperton Fracture Zone north-northwest of the Manihiki Plateau. Ocean crust in this region formed during Cretaceous long magnetic normal Chron 34. Larson (Geology, 25, 779) argued that the NCT is part of an aborted rift system that formed between the Ontong Java and Manihiki plume heads, and terminated plateau construction around 120 Ma via drain-off of plume mantle to the region of rifting. Taylor (EPSL, 241, 372) instead proposed the two plateaus formed as one short-lived mega-plateau that broke apart, and that the NCT is part of the post-breakup transform system that separated a series of short spreading segments. Recently, the R.V. Kilo Moana dredged four sites along the prominent north-facing escarpment of the NCT between 168° 06' W and 168° 42' W at ~1° 24' S, and retrieved basalt, diabase, gabbro, pyroxenite, peridotite, serpentinite, breccias and sedimentary rocks. The diversity of rock types recovered demonstrates that a large cross-section through Cretaceous seafloor is exposed. The MgO content of the basalt and diabase samples varies from 8.9-4.3 wt.%. Incompatible element patterns display relative depletions in alteration- resistant large-ion lithophile elements, and most samples have a distinctive hump-shaped REE pattern, with chondrite-normalized (Sm/Yb)n >1.3 and (La/Sm)n <0.75, suggesting generation by high pressure, relatively low-degree melting of a MORB-type mantle source. One sample is less light-REE- depleted, with (La/Sm)n= 0.96. Age-adjusted (to 120 Ma) Nd-Pb isotope ratios plot within the high- 206Pb/204Pb portion of the Pacific MORB field at ɛNd values between +8.2 and +7.5. In contrast, data for the Ontong Java and Manihiki plateaus fall well below the Pacific MORB field at lower 206Pb/204Pb and ɛNd < +6.6. Thus, our data provide no evidence for Ontong Java or Manihiki mantle components in the NCT source.

  9. Geochemistry and petrogenesis of carbonatites from South Nam Xe, Lai Chau area, northwest Vietnam

    NASA Astrophysics Data System (ADS)

    Nguyen Thi, Thuy; Wada, Hideki; Ishikawa, Tsuyoshi; Shimano, Taketo

    2014-06-01

    This paper presents a study of the petrography, mineral chemistry, geochemistry, and Sr-Nd-Pb-C-O isotope systematics of carbonatite dykes and associated rocks from the northeastern part of the Song Da intracontinental rift in South Nam Xe (northwest Vietnam) aimed at constraining the origin of the carbonatite magmas. The carbonatites are characterized by SiO2 < 12.18 wt.% and by wide ranges in FeO, MgO and CaO content that define them as calciocarbonatite and ferrocarbonatite. On U-Th-Pb isochron diagrams, whole rocks and mineral separates from the ferrocarbonatites form linear arrays corresponding to ages of 30.2-31.6 Ma (Rupelian, Oligocene). The South Nam Xe carbonatites are extremely enriched in Sr, Ba, and light rare earth elements (LREE), and depleted in high field strength elements (HFSE) (e.g. Ti, Nb, Ta, Zr and Hf). The age-corrected Sr-Nd-Pb isotope ratios and C isotope data are relatively uniform (87Sr/86Sr(t) = 0.708193-0.708349; 143Nd/144Nd(t) = 0.512250-0.512267; ɛNd(t) = -6.46 to -6.80; 206Pb/204Pb(t) = 18.26-18.79; 207Pb/204Pb(t) = 15.62-15.64; 208Pb/204Pb(t) = 38.80-39.38; δ13CV-PDB = -2.7 ‰ to -4.1 ‰). These isotopic compositions indicate source contamination that occurred before the production of the carbonatite magmas, and did not change noticeably during or after emplacement. The variation in oxygen isotopes is consistent with the change in mineral compositions and trace element abundances: the lower δ18O values (9.1-11.0 ‰) coupled with Sr-rich, Mn-poor calcite, and igneous textures such as triple junctions among calcite grain boundaries, define a magmatic origin. However, the elevated δ18O values of the ferrocarbonatites (12.0-13.3 ‰) coupled with a volatile-bearing mineral assemblages (including REE fluorcarbonates, sulfates, sulfides and fluorite) may be due to interaction with meteoric water during low-temperature alteration. High δ13C values and Sr-Pb ratios, and low Rb/Sr (0.00014-0.00301), Sm/Nd (0.089-0.141) and 143Nd/144

  10. The geology of the carbonate-hosted Blende Ag-Pb-Zn deposit, Wernecke Mountains, Yukon, Canada

    NASA Astrophysics Data System (ADS)

    Moroskat, Micheal; Gleeson, Sarah A.; Sharp, R. J.; Simonetti, A.; Gallagher, C. J.

    2015-01-01

    The Ag-Zn-Pb Blende deposit is located in the Wernecke Mountains, Yukon and is hosted by the middle Proterozoic Gillespie Lake Group dolomitic siltstones. The sulphide mineralization is localized within the axial planar cleavage of a kilometre-scale anticline and is dominated by galena- and sphalerite-cemented mosaic, rubble and crackle breccias with minor pyrite, galena, sphalerite and dolomite veins. 206Pb/204Pb values from galena range from 16.355 to 16.600, 207Pb/204Pb from 15.430 to 15.461, and 208Pb/204Pb from 36.016 to 36.283, respectively, and yield model ages between 1,490 and 1,430 Ma. A hydrothermal alteration zone, which is younger than the mineralization, has a poorly constrained U-Pb monazite age of 1,307 ± 180 Ma, which suggests that the Blende deposit is Proterozoic in age. Dolomites associated with the main- and late-stage mineralization have δ13C values that range from -1.8 to 0.9 ‰ and δ18O values of 15.7 to 21.9 ‰. The total range of δ34S values from pyrite, galena and sphalerite is 9.4 to 58.1 ‰, indicating that the sulphur in the deposit was derived from reduction of seawater sulphate in a closed system. Strontium isotopes suggest there were three fluids involved in the Blende mineralizing system: Fluid 1 was derived from seawater and formed carbonate and quartz veins pre-mineralization; it has an 87Sr/86Sr ratio of 0.70948. Fluid 2 has a high 87Sr/86Sr ratio of 0.73866, and fluid 3 has a Sr isotopic ratio of 0.71602. Fluids 1 and 3 have similar isotopic compositions but different total Sr ion signals (a function of concentration). This suggests that fluids 1 and 3 may have ultimately been derived from Proterozoic seawater but have undergone different amounts of water-rock interaction. The isotopic and geochemical data suggest the mineralization formed when a H2S-rich fluid derived from seawater (fluid 3) mixed with a metal-bearing fluid (fluid 2) in the high permeability zones of the axial planar cleavage. The Blende deposit is an

  11. Geochemical and Sr-Nd-Pb Isotopic Insights of the Low-Ti basalts from Paraná-Etendeka Igneous Province, Southern Brazil: Constraints on Petrogenesis and the Role of Crustal Contamination

    NASA Astrophysics Data System (ADS)

    Raposo, I.; Barreto, C. J.; Lima, E. F. D.; Lafon, J. M.; Sommer, C. A.; Waichel, B. L.

    2015-12-01

    The south hinge of the Torres Syncline in southernmost Brazil hosts a volcanic succession of pahoehoe and rubbly Gramado-type lavas belonging to the ~132 Ma Paraná-Etendeka Igneous Province. We employ local-scale stratigraphy in three distinct profiles (Santa Cruz do Sul-Herveiras, Morro da Cruz and Lajeado geologic sections) as guidelines for geochemical and Sr-Nd-Pb isotope studies in order to discuss the petrogenesis of lava flows in a single magma type and to quantitatively evaluate the role of crustal contamination and the potential contaminants involved. In all profiles, the lava flows exhibit compositions ranging from basalt to andesite with tholeiitic affinity. The compositional and isotopic variations are not systematic according to stratigraphy, implying that the magma chamber could have undergone periodic replenishments or distinct magma pulses through time or multiple plumbling systems may have existed. The andesites (SiO2 55-58 wt.%) with ponded pahoehoe morphology represent evolved melts at early stages of volcanism with strong susceptibility to crustal contamination as they established pathways to the surface. The olivine basalts (SiO2 47-50 wt.%) and basaltic andesites (SiO2 51-56 wt.%) showing compound morphology and simple pahoehoe morphology, respectively, could be explained by longer time residence of liquids in the crust with higher degrees of crustal assimilation than the ponded pahoehoe lavas. The basaltic andesites (SiO2 52-56 wt. %) with rubbly morphology are related to late differentiation process in shallow magma chambers. Crustal assimilation process accounts for the high initial 87Sr/86Sr ratios at 0.707798-0.715751, very low ɛNd between -8.36 and -5.41, high 206Pb/204Pb ratios at 18.424-18.865, with intermediate 207Pb/204Pb and 208Pb/204Pb ratios at 15.649-15.710 and 38.618-39.369, respectively. The isotopic variations require assimilation of both Paleoproterozoic and Neoproterozoic contaminants at variable degrees.

  12. Sm-Nd dating and REE Composition of scheelite for the Honghuaerji scheelite deposit, Inner Mongolia, Northeast China

    NASA Astrophysics Data System (ADS)

    Guo, Zhijun; Li, Jinwen; Xu, Xinying; Song, Zeyou; Dong, Xuzhou; Tian, Jing; Yang, Yuncheng; She, Hongquan; Xiang, Anping; Kang, Yongjian

    2016-09-01

    Sm-Nd analyses of seven scheelite samples from scheelite-quartz veins in the Honghuaerji scheelite deposit produce a well-defined linear array on an isochron diagram with a mean square weighted deviation (MSWD) of 0.87 corresponding to an age of 178.4 ± 2.9 Ma with εNd(t) = + 1.50. This age is interpreted to represent the age of scheelite mineralization. The scheelite Sm-Nd age is in good agreement with U-Pb ages obtained from a mineralization-related granite (179.4 ~ 178.6 Ma), indicating that there is no apparent age gap between granite crystallization and ore formation. Rare earth element (REE) abundances in the scheelite were determined by in situ laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), and the scheelite samples contain elevated REE concentrations with total ΣREE + Y contents in the range of 3339 to 6321 ppm. The chondrite-normalized REE distribution patterns of all scheelites are middle REE (MREE)-enriched, with strong negative Eu-anomalies (Eu/Eu* = 0.09 ~ 0.23). The REE characteristics of the Honghuaerji scheelite suggest that REE3 + substituted into the Ca site along with Na and Nb (dominated by Na), whereas Eu is predominantly present as Eu2 + in the scheelite and may have crystallized from relatively reduced fluids. All sulfur isotope data (δ34S) for sulfide separates range from + 2.0 to + 3.8‰, with an average of 3.2‰. Measured 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios vary from 18.243 to 18.451, 15.494 to 15.574, and 37.933 to 38.340, respectively. On the basis of common Sr-Nd-Pb-Hf isotopic characteristics between the scheelite and the host granite and the positive initial Nd isotope ratios (+ 1.46 - + 1.52), low 87Sr/86Sr ratios (0.704983-0.705297) in the scheelites, it is inferred that the hydrothermal fluids responsible for tungsten mineralization at Honghuaerji were of magmatic origin with a mantle-derived signature. Based on the regional geology, tectonic evolution, and geochemical evidence, the

  13. Tracking mobility using human hair: What can we learn from lead and strontium isotopes?

    PubMed

    Vautour, Geneviève; Poirier, André; Widory, David

    2015-01-01

    The isotope ratios of strontium (Sr) and lead (Pb) in water derive from local geology and their isotopic signature can be linked to the age and type of underlying bedrocks and soils (if applicable), and are transferred up the food-chain. Both elements are transferred to human blood through diet and water, and some of it will ultimately be incorporated into the hair structure, making Sr and Pb isotopes interesting tools for tracing human mobility. In this study, we analyzed both the elemental concentration and isotope ratios of Sr and Pb from four different women of different ages to monitor their permanent relocation from central France to Eastern Canada during the summer 2012. For comparison, we also characterized bulk hair samples of sedentary individuals and local tap waters from their regions of origin and of settlement. Our results indicate that the 87Sr/86Sr and 206Pb/204Pb ratios are significantly modified by the change of environment, but also confirm that human hair compositions are impacted by other external factors (such as dust). Sr and Pb isotope systematics demonstrate their added value for detecting human mobility, but require further studies to better constrain the main sources and processes controlling their respective budgets in human hair for provenancing purposes.

  14. [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].

    PubMed

    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.

  15. 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.

    PubMed

    Frostick, A; Bollhöfer, A; Parry, D

    2011-10-01

    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 #2, south of the Ranger mineral lease, exhibit radiogenic (206)Pb/(207)Pb and (208)Pb/(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.

  16. Lead isotopes in North Pacific deep water - Implications for past changes in input sources and circulation patterns

    USGS Publications Warehouse

    van de Flierdt, T.; Frank, M.; Halliday, A.N.; Hein, J.R.; Hattendorf, B.; Gunther, D.; Kubik, P.W.

    2003-01-01

    The sources of non-anthropogenic Pb in seawater have been the subject of debate. Here we present Pb isotope time-series that indicate that the non-anthropogenic Pb budget of the northernmost Pacific Ocean has been governed by ocean circulation and riverine inputs, which in turn have ultimately been controlled by tectonic processes. Despite the fact that the investigated locations are situated within the Asian dust plume, and proximal to extensive arc volcanism, eolian contributions have had little impact. We have obtained the first high-resolution and high-precision Pb isotope time-series of North Pacific deep water from two ferromanganese crusts from the Gulf of Alaska in the NE Pacific Ocean, and from the Detroit Seamount in the NW Pacific Ocean. Both crusts were dated applying 10 Be/9Be ratios and yield continuous time-series for the past 13.5 and 9.6 Myr, respectively. Lead isotopes show a monotonic evolution in 206Pb/204Pb from low values in the Miocene (??? 18.57) to high values at present day (??? 18.84) in both crusts, even though they are separated by more than 3000 km along the Aleutian Arc. The variation exceeds the amplitude found in Equatorial Pacific deep water records by about three-fold. There also is a striking similarity in 207Pb/204Pb and 208Pb/ 204Pb ratios of the two crusts, indicating the existence of a local circulation cell in the sub-polar North Pacific, where efficient lateral mixing has taken place but only limited exchange (in terms of Pb) with deep water from the Equatorial Pacific has occurred. Both crusts display well-defined trends with age in Pb-Pb isotope mixing plots, which require the involvement of at least four distinct Pb sources for North Pacific deep water. The Pb isotope time-series reveal that eolian supplies (volcanic ash and continent-derived loess) have only been of minor importance for the dissolved Pb budget of marginal sites in the deep North Pacific over the past 6 Myr. The two predominant sources have been young

  17. Timescales of magma differentiation from basalt to andesite beneath Hekla Volcano, Iceland: Constraints from U-series disequilibria in lavas from the last quarter-millennium flows

    NASA Astrophysics Data System (ADS)

    Chekol, Takele A.; Kobayashi, Katsura; Yokoyama, Tetsuya; Sakaguchi, Chie; Nakamura, Eizo

    2011-01-01

    Measurements of 238U- 230Th- 226Ra disequilibria, Sr-Nd-Pb-Hf isotopes and major-trace elements have been conducted for lavas erupted in the last quarter-millennium at Hekla volcano, Iceland. The volcanic rocks range from basalt to dacite. Most of the lavas (excluding dacitic samples) display limited compositional variations in radiogenic Sr-Nd-Pb-Hf isotopes ( 87Sr/ 86Sr = 0.70319-0.70322; 143Nd/ 144Nd = 0.51302-0.51305; 206Pb/ 204Pb = 19.04-19.06; 207Pb/ 204Pb = 15.53-15.54; 208Pb/ 204Pb = 38.61-38.65; 176Hf/ 177Hf = 0.28311-0.28312). All the samples possess ( 230Th/ 238U) disequilibrium with 230Th excesses, and they show systematic variations in ( 230Th/ 232Th) and ( 238U/ 232Th) ratios. The highest 226Ra excesses occur in the basalt and most differentiated andesite lavas, while some basaltic-andesite lavas have ( 226Ra/ 230Th) ratio that are close to equilibrium. The 238U- 230Th- 226Ra disequilibria variations cannot be produced by simple closed-system fractional crystallization with radioactive decay of 230Th and 226Ra in a magma chamber. A closed-system fractional crystallization model and assimilation and fractional crystallization (AFC) model indicate that the least differentiated basaltic andesites were derived from basalt by fractional crystallization with a differentiation age of ˜24 ± 11 kyr, whereas the andesites were formed by assimilation of crustal material and fractionation of the basaltic-andesites within 2 kyr. Apatite is inferred to play a key role in fractionating the parent-daughter nuclides in 230Th- 238U and 226Ra- 230Th to make the observed variations. Our proposed model is that several batches of basaltic-andesite magmas that formed by fractional crystallization of a basaltic melt from a deeper reservoir, were periodically injected into the shallow crust to form individual magma pockets, and subsequently modifying the original magma compositions via simultaneous assimilation and fractional crystallization. The assimilant is the dacitic

  18. Source heterogeneity for the major components of ˜ 3.7 Ga Banded Iron Formations (Isua Greenstone Belt, Western Greenland): Tracing the nature of interacting water masses in BIF formation

    NASA Astrophysics Data System (ADS)

    Frei, Robert; Polat, Ali

    2007-01-01

    We report trace element, samarium (Sm)-neodymium (Nd) and lead (Pb) isotopic data for individual micro-and mesobands of the Earth's oldest Banded Iron Formation (BIF) from the ˜ 3.7-3.8 Ga Isua Greenstone Belt (IGB, West Greenland) in an attempt to contribute to the characterization of the depositional environment and to the understanding of depositional mechanisms of these earliest chemical sediments. Rare earth element (REE)-yttrium (Y) patterns of the individual mesobands show features of modern seawater with diagnostic cerium (Ce/Ce *), presodymium (Pr/Pr *) and Y/holmium (Ho) anomalies. Very low high field strength elements (HFSE) concentrations indicate essentially detritus-free precipitation. Uranogenic Pb isotope data define a correlation line with a slope of 3691 ± 41 Ma, indicating that the uranium (U)-lead (Pb) system remained closed after the formation of this BIF. High 207Pb/ 204Pb relative to 206Pb/ 204Pb ratios compared to average mantle growth evolution models are a feature shared by BIF, penecontemporaneous basalts and clastic volcanogenic metasediments and are indicative of the ultimate high-μ ( 238U/ 204Pb) character of the source region, an essentially mafic Hadean protocrust. Sm-Nd isotopic relations on a layer-by-layer basis point to two REE sources controlling the back-arc basin depositional environment of the BIF, one being seafloor-vented hydrothermal fluids ( ɛNd (3.7 Ga) ˜ + 3.1), the other being ambient surface seawater which reached its composition by erosion of parts of the protocrustal landmass ( ɛNd(3.7 Ga) ˜ + 1.6). The validity of two different and periodically interacting water masses (an essentially two-component mixing system) in the deposition of alternating iron- and silica-rich layers is also reflected by systematic trends in germanium (Ge)/silicon (Si) ratios. These suggest that significant amounts of silica were derived from unexposed and/or destroyed mafic Hadean landmass, unlike iron which probably originated from

  19. Source Heterogeneity for the Major Components of ~3.7 Ga Banded Iron Formations (Isua Greenstone Belt, Western Greenland): Tracing the Nature of Interacting Water Masses in BIF formation.

    NASA Astrophysics Data System (ADS)

    Frei, R.; Polat, A.

    2006-12-01

    We report trace element, Sm-Nd and Pb isotopic data for individual micro- and mesobands of the Earth's oldest Banded Iron Formation (BIF) from the ~3.7-3.8 Ga Isua Greenstone Belt (IGB, West Greenland) in an attempt to contribute to the characterization of the depositional environment and to the understanding of depositional mechanisms of these earliest chemical sediments. REE-Y patterns of the individual mesobands show features of modern seawater with diagnostic Ce/Ce*, Pr/Pr* and Y/Ho anomalies. Very low HFSE concentrations indicate essentially detritus-free precipitation. Uranogenic Pb isotope data define a correlation line with a slope of 3691 ± 41 Ma, indicating that the U-Pb system remained closed after the formation of this BIF. High 207Pb/204Pb relative to 206Pb/204Pb ratios compared to average continental growth evolution models are a feature shared by BIF, penecontemporaneous basalts and clastic volcanogenic metasediments and are indicative of the ultimate high-μ (238U/204Pb) character of the source region, an essentially mafic Hadean protocrust. Sm-Nd isotopic relations on a layer-by-layer basis point to two REE sources controlling the back-arc basin depositional environment of the BIF, one being seafloor-vented hydrothermal fluids (ɛ Nd (3.7 Ga) ~+3.1), the other being ambient surface seawater which reached its composition by erosion of parts of the protocrustal landmass (ɛ Nd(3.7 Ga) ~+1.6). The validity of two different and periodically interacting water masses (an essentially two-component mixing system) in the deposition of alternating iron- and silica-rich layers is also reflected by systematic trends in Ge/Si ratios. These imply that significant amounts of silica were derived from unexposed and/or destroyed mafic Hadean landmass, unlike iron which probably originated from oceanic crust following hydrothermal alteration by deep percolating seawater. Ge/Si distributional patterns in the early Archean Isua BIF are similar to those reported from

  20. Petrogenesis of the Yaochong granite and Mo deposit, Western Dabie orogen, eastern-central China: Constraints from zircon U-Pb and molybdenite Re-Os ages, whole-rock geochemistry and Sr-Nd-Pb-Hf isotopes

    NASA Astrophysics Data System (ADS)

    Chen, Wei; Xu, Zhaowen; Qiu, Wenhong; Li, Chao; Yu, Yang; Wang, Hao; Su, Yang

    2015-05-01

    The Dabie orogen is among the most famous continent-continent collisional orogenic belts in the world, and is characterized by intensive post-collisional extension, magmatism and Mo mineralization. However, the genetic links between the mineralization and the geodynamic evolution of the orogen remain unresolved. In this paper, the Yaochong Mo deposit and its associated granitic stocks were investigated to elucidate this issue. Our new zircon U-Pb ages yielded an Early Cretaceous age (133.3 ± 1.3 Ma) for the Yaochong granite, and our molybdenite Re-Os dating gave a similar age (135 ± 1 Ma) for the Mo deposit. The Yaochong stock is characterized by high silica and alkali but low Mg, Fe and Ca. It is enriched in light rare earth elements (LREEs) and large ion lithophile elements (LILEs: Rb, K, Th and U), but strongly depleted in heavy REEs, and high field strength elements (HFSEs: Nb, Ta, Ti and Y). The Yaochong granite has initial 87Sr/86Sr ratios of 0.7087-0.7096, and Pb isotopic ratios of (206Pb/204Pb)i = 16.599-16.704, (207Pb/204Pb)i = 15.170-15.618 and (208Pb/204Pb)i = 36.376-38.248. The granite has εNd(t) of -18.0 to -16.3 and εHf(t) values of -26.5 to -20.0. All these data indicate that the Yaochong granite is a high-K calc-alkaline fractionated I-type granite, and may have originated from partial melting of the thickened Yangtze continental crust. The Mo ores also show low radiogenic Pb isotopes similar to the Yaochong stock. Medium Re content in molybdenite (21.8-74.8 ppm) also suggests that the ore-forming materials were derived from the thickened lower crust with possibly minor mixing with the mantle. Similar to the Eastern Dabie orogen, the thickened crust beneath the Western Dabie orogen may also have experienced tectonic collapse, which may have exerted fundamental geodynamic controls on the two-stage Mo mineralization in the region.

  1. Hafnium isotope variations in oceanic basalts.

    USGS Publications Warehouse

    Patchett, P.J.; Tatsumoto, M.

    1980-01-01

    Routine low-blank chemistry and 0.01-0.04% precision on the ratio 176Hf/177Hf allows study of Hf isotopic variations, generated by beta --decay of 176Lu, in volcanic rocks derived from the suboceanic mantle. Normalized to 176Hf/177Hf = 0.7325, 176Hf/177Hf ranges 0.2828-0.2835, based on 24 basalt samples. 176Hf/177Hf is positively correlated with 143Nd/144Nd, and negatively correlated with 87Sr/86Sr and 206Pb/204Pb. Along the Iceland-Reykjanes ridge traverse, 176Hf/177Hf increases southwards. The coherence of Hf, Nd and Sr isotopes in the oceanic mantle allows an approximate bulk Earth 176Hf/177Hf of 0.28295 to be inferred from the bulk Earth 143Nd/144Nd. This requires the bulk Earth Lu/Hf to be 0.25, similar to that of the Juvinas eucrite. 60% of the Hf isotopic variation in oceanic basalts occurs among mid-ocean ridge samples. Lu-Hf fractionation probably decouples from Sm-Nd and Rb-Sr fractionation in very depleted source regions, with high Lu/Hf, and consequent high 176Hf/177Hf ratios developing in mantle residual from partial melting. (Authors' abstract) -T.R.

  2. Pb, Sr, and Nd isotopes in seamount basalts from the Juan de Fuca Ridge and Kodiak-Bowie seamount chain, northeast Pacific

    USGS Publications Warehouse

    Hegner, E.; Tatsumoto, M.

    1989-01-01

    Pb, Sr, and Nd isotopic ratios and their parent/daughter element concentrations for 28 basalts from 10 hotspot and nonhotspot seamounts are reported. Nd and Sr isotopic compositions (143Nd/144Nd = 0.51325-0.51304; 87Sr/86Sr = 0.70237-0.70275) plot in the envelope for Juan de Fuca-Gorda ridge basalts with tholeiitic basalts showing more depleted sources and a better negative correlation than transitional to alkalic basalts. Pb isotopic ratios in tholeiitic and alkalic basalts overlap (206Pb/204Pb = 18.29-19.44) and display a trend toward more radiogenic Pb in alkalic basalts. The isotopic data for hotspot and nonhotspot basalts are indistinguishable and correlate broadly with rock composition, implying that they are controlled by partial melting. The isotopic variation in the seamount basalts is about 60% (Nd-Sr) to 100% (Pb) of that in East Pacific Rise basalts and is interpreted as a lower limit for the magnitude of mantle heterogeneity in the northeast Pacific. The data indicate absence of a chemically distinct plume component in the linear seamount chains and strongly suggest an origin from mid-ocean ridge basalt-like east Pacific mantle. -Authors

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

    PubMed

    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.

  4. Using stable lead isotopes to trace heavy metal contamination sources in sediments of Xiangjiang and Lishui Rivers in China.

    PubMed

    Sun, Guo-Xin; Wang, Xin-Jun; Hu, Qin-Hong

    2011-12-01

    Lead isotopes and heavy metal concentrations were measured in two sediment cores sampled in estuaries of Xiangjiang and Lishui Rivers in Hunan province, China. The presence of anthropogenic contribution was observed in both sediments, especially in Xiangjiang sediment. In the Xiangjiang sediment, the lower (206)Pb/(207)Pb and higher (208)Pb/(206)Pb ratio, than natural Pb isotope signature (1.198 and 2.075 for (206)Pb/(207)Pb and (208)Pb/(206)Pb, respectively), indicated a significant input of non-indigenous Pb with low (206)Pb/(207)Pb and high (208)Pb/(206)Pb. The corresponding concentrations of heavy metals (As, Cd, Zn, Mn and Pb) were much higher than natural values, suggesting the contaminations of heavy metals from extensive ore-mining activities in the region.

  5. Geochemical and isotopic perspectives on the origin and evolution of the Siletzia Terrane.

    NASA Astrophysics Data System (ADS)

    Phillips, B. A.; Weis, D.; Mullen, E.; Kerr, A. C.

    2015-12-01

    The Siletzia terrane, located in the Cascadia forearc region of Oregon, Washington and Vancouver Island, consists of a series of accreted basaltic pillow lavas, massive flows and intrusive sheets. It represents a late Paleocene-Eocene oceanic large igneous province (LIP), previously proposed to represent an accreted oceanic plateau, hotspot island chain, backarc basin, island arc, or a sequence of slab window volcanics formed by ridge subduction. A province-wide geochemical reassessment of the terrane, including new high precision Sr-Pb-Nd-Hf isotope data on basaltic samples, has been used to assess the validity of the proposed tectonomagmatic models for Siletzia. The trace element data show REE patterns that are flat to LREE enriched with an absence of any arc signatures. These features are comparable to other oceanic plateaus such as the Ontong Java and the Caribbean and so therefore support a mantle plume origin. Initial isotope ratios range from 206Pb/204Pb = 18.869 - 19.673, 207Pb/204Pb = 15.527 - 15.609, 208Pb/204Pb = 38.551 - 39.220, ɛHf = +9.0 - 14.8, ɛNd = +5.0 - 8.0 and 87Sr/86Sr = 0.70304 - 0.70397. The isotope signatures become more varied southward across the terrane and reveal two trends: i) HIMU-DMM and ii) another extending from DMM towards the Imnaha component, thought to represent the mantle plume source of the Columbia River Basalts and Yellowstone 1,2. The data may support the previously proposed idea that the volcanism of the Siletzia terrane represents initial melting of the mantle plume head of the Yellowstone hotspot 3,4,5. Other evidence indicating a LIP origin includes the relatively rapid eruption/intrusion of an estimated magma volume of 2.6 x 106 km3 6 between ~56-49 Ma 5, which, in conjunction with our new elemental and isotopic data, indicates that the Siletzia terrane most likely represents an accreted oceanic plateau. 1. Wolff et al., (2008) Nature Geoscience 1, 177-180. 2. Jean et al., (2014) EPSL 389, 119-131 3. Duncan (1982

  6. Isotope geochemistry and fluid inclusion study of skarns from Vesuvius

    USGS Publications Warehouse

    Gilg, H.A.; Lima, A.; Somma, R.; Belkin, H.E.; de Vivo, B.; Ayuso, R.A.

    2001-01-01

    We present new mineral chemistry, fluid inclusion, stable carbon and oxygen, as well as Pb, Sr, and Nd isotope data of Ca-Mg-silicate-rich ejecta (skarns) and associated cognate and xenolithic nodules from the Mt. Somma-Vesuvius volcanic complex, Italy. The typically zoned skarn ejecta consist mainly of diopsidic and hedenbergitic, sometimes "fassaitic" clinopyroxene, Mg-rich and Ti-poor phlogopite, F-bearing vesuvianite, wollastonite, gehlenite, meionite, forsterite, clinohumite, anorthite and Mg-poor calcite with accessory apatite, spinell, magnetite, perovskite, baddeleyite, and various REE-, U-, Th-, Zr- and Ti-rich minerals. Four major types of fluid inclusions were observed in wollastonite, vesuvianite, gehlenite, clinopyroxene and calcite: a) primary silicate melt inclusions (THOM = 1000-1050??C), b) CO2 ?? H2S-rich fluid inclusions (THOM = 20-31.3??C into the vapor phase), c) multiphase aqueous brine inclusions (THOM = 720-820??C) with mainly sylvite and halite daughter minerals, and d) complex chloride-carbonate-sulfate-fluoride-silicate-bearing saline-melt inclusions (THOM = 870-890??C). The last inclusion type shows evidence for immiscibility between several fluids (silicate melt - aqueous chloride-rich liquid - carbonate/sulfate melt?) during heating and cooling below 870??C. There is no evidence for fluid circulation below 700??C and participation of externally derived meteoric fluids in skarn formation. Skarns have considerably variable 206Pb/204Pb (19.047-19.202), 207Pb/204Pb (15.655-15.670), and 208Pb/204Pb (38.915-39.069) and relatively low 143Nd/144Nd (0.51211-0.51244) ratios. The carbon and oxygen isotope compositions of skarn calcites (??13CV-PDB = -5.4 to -1.1???; ??18OV-SMOW = 11.7 to 16.4???) indicate formation from a 18O- and 13C-enriched fluid. The isotope composition of skarns and the presence of silicate melt inclusion-bearing wollastonite nodules suggests assimilation of carbonate wall rocks by the alkaline magma at moderate depths (< 5

  7. Petrology and Geochemistry of the Eocene Volcanic Rocks in the Kahrizak Mountains, Central Iran

    NASA Astrophysics Data System (ADS)

    Yazdani, S.; Castillo, P.; Tutti, F.

    2013-12-01

    The Eocene volcanic rocks in the Kahrizak (KH) Mountains in the northern part of Central Iran were mainly formed by magmatism that accompanied block-faulting tectonism in the region. In the KH area, the volcanic rocks are nonconformably overlain by Oligocene-Pliocene sedimentary deposits, suggesting that the Eocene magmatic activity in the region was followed by a sequence of uplift and shallow marine regression. The volcanic rocks consist of pyroclastics (tuff and ignimbrites) and lava flows (basalt, basaltic trachyandesite, trachyandesite, and rhyolite); superposition indicates an earlier explosive volcanic phase that caused the widespread distribution of rhyolitic ignimbrites and tuffs, and this was followed by a quieter phase of lava eruptions. Petrographic evidence such as mineral zoning, sieve texture and rounded crystals of plagioclase and pyroxene phenocrysts indicate non-equilibrium conditions between melt and crystals during magma cooling. These textures suggest magma mixing, although these may also be due to rapid decompression, where heat loss is minor relative to the ascent rate. The geochemistry of KH samples indicates their subalkaline to alkaline affinity. In terms of trace element contents, most samples exhibit the distinct geochemical trait of arc volcanism, i.e., Nb and Ta depletions relative to LILE (e.g., Ba, Rb) enrichment and positive Sr anomaly; however, Zr and Ti depletions are not prominent. The samples have a light-REE enriched but flat heavy-REE pattern and negative Eu anomaly in the rhyolites and trachyandesites. They have a ~narrow to ~moderate range of Pb isotopic ratios (206Pb/204Pb ~18.6-18.9, 207Pb/204Pb ~15.5-15.6, and 208Pb/204Pb ~38.5-38.8), with basaltic rocks somewhat higher than rhyolitic rocks. Available geochemical and isotopic data suggest a complex origin and evolution of the KH magmas. The magmas originated from an intrinsically ~heterogeneous source and, in addition to fractional crystallization, some of the

  8. Magmas with slab fluid and decompression melting signatures coexisting in the Gulf of Fonseca: Evidence from Isla El Tigre volcano (Honduras, Central America)

    NASA Astrophysics Data System (ADS)

    Mattioli, Michele; Renzulli, Alberto; Agostini, Samuele; Lucidi, Roberto

    2016-01-01

    Isla El Tigre volcano is located in the Gulf of Fonseca (Honduras) along the Central America volcanic front, where a significant change in the strike of the volcanic chain is observed. The studied samples of this poorly investigated volcano are mainly subalkaline basic to intermediate lavas (basalts and basaltic andesites) and subordinate subalkaline/alkaline transitional basalts, both having the typical mineralogical and geochemical characteristics of arc volcanic rocks. On the basis of petrographic and geochemical features, two groups of rocks have been distinguished. Lavas from the main volcanic edifice are highly porphyritic and hy-qz normative, and have lower MgO contents (< 5 wt.%). They show significant LILE and LREE enrichments and Nb-Ta depletions, and have a strong slab signature as well as incompatible element contents similar to those of the main front of the adjacent volcanoes in El Salvador and Nicaragua (e.g., Ba/La up to 80). In contrast, lavas from the parasitic cones have higher MgO contents (> 5 wt.%), are ol-hy normative and show lower HFSE depletions relative to LILE and LREE, with lower Ba/La, Ba/Nb and Zr/Nb ratios. This suggests that mantle-derived magmas were not produced by the same process throughout the activity of the volcano. The bulk rock geochemistry and 87Sr/86Sr (0.70373-0.70382), 143Nd/144Nd (0.51298-0.51301), 206Pb/204Pb (18.55-18.58), 207Pb/204Pb (15.54-15.56) and 208Pb/204Pb (38.23-38.26) isotopic data of Isla El Tigre compared with the other volcanoes of the Gulf of Fonseca and all available literature data for Central America suggests that this stratovolcano was mainly built by mantle-derived melts driven by slab-derived fluid-flux melting, while magmas erupted through its parasitic cones have a clear signature of decompression melting with minor slab contribution. The coexistence of these two different mantle melting generation processes is likely related to the complex geodynamic setting of the Gulf of Fonseca, where the

  9. Geochronology and geochemistry of Eocene potassic felsic intrusions in the Nangqian basin, eastern Tibet: Tectonic and metallogenic implications

    NASA Astrophysics Data System (ADS)

    Xu, Yue; Bi, Xian-Wu; Hu, Rui-Zhong; Chen, You-wei; Liu, He-qing; Xu, Lei-luo

    2016-03-01

    The Jinshajiang-Ailaoshan copper belt is the most significant porphyry copper belt in eastern Tibet. In the northern segment of this belt within the Nangqian basin, which occurs 100 km east of the Yulong porphyry copper deposit, several felsic intrusions have been recently discovered. The Yulong porphyry copper deposit is one of the largest porphyry copper deposits in China, and it is associated with peraluminous adakitic rocks formed in a post-collisional setting. The Nangqian felsic intrusions vary from syenite porphyry to monzonite porphyry in rock types. No significant Cu-Au mineralization has been found in the Nangqian felsic intrusions despite extensive exploration in recent years. LA-ICP-MS zircon U-Pb dating reveals that the Nangqian syenite porphyry and monzonite porphyry were emplaced at ~ 35.6±0.3 Ma and from 39.5±0.3 to 37.4±0.3 Ma, respectively, similar to the age of the Yulong porphyry copper deposit. The Nangqian felsic intrusions are characterized by metaluminous compositions (A/CNK = 0.82-1.01), and they share some common features with shoshonites such as high K2O contents (4.58-5.58 wt.%), high K2O/Na2O ratios (0.92-1.28), LREE-LILE enrichments and negative Nb-Ta-Ti-P anomalies, as well as with adakites derived from an eclogite-facies source with high Al2O3 (14.98-15.74 wt.%), Sr (954-2190 ppm), Sr/Y (68-132) and La/Yb (53-85), and low Y and Yb contents. The Nangqian felsic intrusions have high initial 87Sr/86Sr (0.7050-0.7055), variable εNd(t) (- 0.31-1.43) and small variations in (206Pb/204Pb)i (18.68-18.74), (207Pb/204Pb)i (15.53-15.62) and (208Pb/204Pb)i (38.51-38.80). Zircon crystals from both syenite and monzonite porphyries are characterized by positive εHf(t) from 5.2 to 8.5. The results suggest that the syenite and monzonite magmas were differentiated from parental shoshonitic melts by fractional crystallization of olivine, clinopyroxene and minor feldspar. The parent magmas originated from a lithospheric mantle metasomatized by slab

  10. A Coast Mountains provenance for the Valdez and Orca groups, southern Alaska, based on Nd, Sr, and Pb isotopic evidence

    USGS Publications Warehouse

    Farmer, G.L.; Ayuso, R.; Plafker, G.

    1993-01-01

    Nd, Sr, and Pb isotopic data were obtained for fourteen fine- to coarse-grained samples of accreted flysch of the Late Cretaceous and early Tertiary Valdez and Orca Groups in southern Alaska to determine the flysch provenance. Argillites and greywackes from the Orca Group, as well as compositionally similar but higher metamorphic grade rocks from the Valdez Group, show a restricted range of correlated ??{lunate}Nd ( -0.6 to -3.8) and 87Sr 86Sr (0.7060-0.7080) at the time of sediment deposition ( ??? 50 Ma). Pb isotopic compositions also vary over a narrow range ( 206Pb 204Pb = 19.138-19.395, 207Pb 204Pb = 15.593-15.703, 208Pb 204Pb = 38.677-39.209), and in the Orca Group the samples generally become more radiogenic with decreasing ??{lunate}Nd and increasing 87Sr 86Sr. All samples have similar trace element compositions characterized by moderate light rare earth element enrichments, and low ratios of high field strength elements to large ion lithophile elements. Based on petrographic, geochemical, and isotopic data the sedimentary rocks are interpreted to have been derived largely from a Phanerozoic continental margin arc complex characterized by igneous rocks with ??{lunate}Nd values between 0 and -5. The latter conclusion is supported by the ??{lunate}Nd values of a tonalite clast and a rhyodacite clast in the Orca Group (??{lunate}Nd = -4.9 and -0.9, respectively). However, trondjemitic clasts in the Orca Group have significantly lower ??{lunate}Nd ( ??? -10) and require a derivation of a portion of the flysch from Precambrian crustal sources. The Nd, Sr, and Pb isotopic compositions of both the Valdez and Orca Groups overlap the values determined for intrusive igneous rocks exposed within the northern portion of the Late Cretaceous to early Tertiary Coast Mountains Plutonic Complex in western British Columbia and equivalent rocks in southeastern Alaska. The isotopic data support previous conclusions based on geologic studies which suggest that the flysch was

  11. Geochemical heterogeneities within the Crozet hotspot

    NASA Astrophysics Data System (ADS)

    Breton, Thomas; Nauret, François; Pichat, Sylvain; Moine, Bertrand; Moreira, Manuel; Rose-Koga, Estelle F.; Auclair, Delphine; Bosq, Chantal; Wavrant, Laurène-Marie

    2013-08-01

    The Crozet Plateau is a 54 Ma-old volcanic plateau that supports five islands characterized by recent volcanic manifestations that are the surface expression of a deep-mantle plume. Due to their remote location and difficult access, the Crozet Islands are poorly sampled. Both the petrological descriptions and geochemical data are scarce. Thus, the sources of the Crozet plume are still under debate. Similarly, the interactions between the Southwest Indian Ridge (SWIR) and the Crozet plume remain questioned. Here, we present a new set of isotopes (Pb, Sr, Nd and He), major and trace elements data on basalts from three islands of the Crozet Archipelago: Penguins, East, and Possession Islands. Our main purpose is to characterize the sources of the Crozet plume and to test its influence at regional scale. Two groups of lavas can be distinguished based on the isotopic data: East and Possession lavas, and Penguins lavas. Principal component analyses on our high-precision Pb isotopes data and literature data show that two mantle sources can explain most of the geochemical variability measured in Crozet lavas. A third minor contribution is however needed to fully explain the data. The entire set of isotopic compositions (Pb, Sr, Nd and He) can be explained by a mixing between three mantle sources: (1) a FOZO (Focus Zone) component, with 206Pb/204Pb higher than 19.5 and high 207Pb/204Pb, 208Pb/204Pb 87Sr/86Sr, 143Nd/144Nd and R/Ra (R/Ra=(He3/He4)sample/(He3/He4)atmosphere) ratios, that is mainly sampled Penguins lavas, (2) a component called “East-Possession” that is mostly sampled by the East-Possession lava group and which presents Pb, Sr and Nd isotope signatures similar to those of the Reunion-Mauritius Islands, and (3) a third minor contribution of the local Depleted MORB Mantle (DMM). The new He isotopes data on the Crozet plume allow us to propose that Crozet plume material is present in the segment of the Southwest Indian Ridge located between the Indomed (ITF

  12. Multiplicity of Magma Source Characteristics and Melting Processes for Late Cenozoic Basalts of the Bering Sea Volcanic Province (BSVP), Alaska

    NASA Astrophysics Data System (ADS)

    Mukasa, S. B.; Andronikov, A. V.

    2006-12-01

    The Bering Sea Volcanic Province consists of a number of large basaltic late Cenozoic volcanic fields in a broad region inboard from the Aleutian arc front to the Arctic Circle, and from Chukchi Peninsula in Russia to Western Alaska, which we have dated by 40Ar/39Ar at ~6.0-0.1 Ma, but with some flows being too young to date by this method. We estimate that >1000 km3 of magma was erupted through the eastern part of the BSVP, all within the past 6 Ma. Combining age information with volume estimates reveals that the intensity of volcanic activity in the region has increased through time, with only about 15% of lava erupted before 3 Ma, and about 45% of all late Cenozoic magma being erupted within the last 300 k.y. Eruption rates also increase toward more recent times: 6-Ma basalts having erupted at the rate of ~70 m3/km2/yr, while the youngest basalts (? 0.7 Ma), are estimated to have erupted at a rate of ~225 m3/km2/yr. All late Cenozoic volcanic rocks are enriched in highly incompatible trace elements with strongly fractionated REE patterns (LaN/YbN = 4.7-23.7) suggesting Grt-bearing source. Nd-Sr-Hf isotopic compositions of the rocks (143Nd/144Nd = 0.512939-0.513139; 87Sr/86Sr = 0.702653-0.704342; 176Hf/177Hf = 0.283098- 0.283257) are similar to those of MORB and the depleted varieties of OIB. Lead isotopic ratios fall mostly below the Northern Hemisphere Reference Line (NHRL) in the Pacific MORB field, but the youngest rocks display a distinct trend toward the EM-II values (206Pb/204Pb = 18.21-19.10; 207Pb/204Pb = 15.42-15.62; 208Pb/204Pb = 37.72-38.88). Regional differences in both trace element and isotopic compositions are apparent, indicating that BSVP magmatism does not have a single origin. Lavas with the arc signature are prevalent near the southern margin of the province while those with an OIB signature dominate the central and northern sectors. Also, selected regions in the province exhibit a systematic increase in 87Sr/86Sr with time (from 0.7027 to up

  13. Geochemical and Sr-Nd-Pb-Os isotopic compositions of Miocene ultrapotassic rocks in southern Tibet: Petrogenesis and implications for the regional tectonic history

    NASA Astrophysics Data System (ADS)

    Wang, BaoDi; Chen, JianLin; Xu, JiFeng; Wang, LiQuan

    2014-11-01

    Ultrapotassic lavas are widespread throughout southern Tibet and are generally thought to have formed from magmas generated by partial melting of an enriched mantle source that was metasomatized during earlier subduction events. Here, we report new geochemical and Sr-Nd-Pb-Os isotope data for Miocene ultrapotassic rocks within the Sailipu area of the western Lhasa terrane, southern Tibet. The Sailipu ultrapotassic rocks are enriched in the large ion lithophile elements relative to the high field strength elements, and have extremely radiogenic Sr (87Sr/86Sr(i) = 0.714480-0.727323), Pb (206Pb/204Pb = 18.414-18.787, 207Pb/204Pb = 15.693-15.749, 208Pb/204Pb = 39.439-39.765), and Os isotopic signatures (187Os/188Os(i) = 0.1095-0.37454), and unradiogenic Nd (εNd(t) = - 11.5 to - 15.2) isotopic compositions. These geochemical and isotopic characteristics, coupled with high K2O (> 5 wt.%) and MgO (5.20-13.70 wt.%) concentrations, Mg# values of 68-76, high Rb/Sr (0.13-0.95) and low Ba/Rb (3.33-12.3) ratios, and the relatively low Os contents and radiogenic Os isotopic compositions of the Sailipu ultrapotassic rocks, do not support any significant crustal contamination. Instead, we consider these rocks to be analogous to the Cenozoic ultrapotassic rocks from Italy and the Balkans, suggesting that they were produced by interaction between melts derived from phlogopite-rich clinopyroxene veins and surrounding peridotitic mantle material. The Sailipu ultrapotassic rocks can be divided into type-1 and type-2 suites based on differences in major and trace element concentrations, and isotopic compositions. Type-1 ultrapotassic rocks are relatively enriched in the heavy rare earth elements, most likely as a result of interaction between melts derived from phlogopite-rich clinopyroxene veins and the surrounding spinel-bearing peridotite material, whereas the type-2 rocks are enriched in rare earth elements and have high (Gd/Yb)N values (8.3-12.2), both of which are indicative of

  14. Who Needs Uranium? Pb-Pb Dating of (and Temporal Resolution in) Zircon

    NASA Astrophysics Data System (ADS)

    Tera, F.

    2002-12-01

    A method akin to Differential Isotope Correlation (Tera, 2000 and 2002) is applied to 204Pb-depleted systems (e. g., zircons), where 206Pb/ 208Pb and 207Pb/ 208Pb are plotted separately versus the same X-axis of 207Pb/ 206Pb or ( 206Pb/ 208Pb)-( 207Pb/ 208Pb). Because of the general transparency of isotopic ratios to recent U-Pb mobility, these correlations usually project less obscured patterns, which are reiterated in the two diagrams. The redundancy allows correlated filtration of aberrant data, thus resulting in sharper lineation. The justification of filtration through redundancy (FTR) is in the concurrent emergence of synchronism (that is, co-incidence of reason) from the two diagrams. Each judiciously filtered line is the result of mixing of two end-members: (1) initial Pb and (2) in-situ produced Pb (through U and Th decay). A system of a single age can have multiple lines, each corresponding to a specific K = Th / U for the in-situ component. If such a system is not complicated beyond recent mobilities, the lines would converge to intersect at a point corresponding to initial Pb (see Fig. 3, Tera, 1983). The {206, 207, 208}Pb plots mentioned are referred to here as Quasi Differential Diagrams. When the data of the filtered lines, obtained as described above, are plotted on an age-producing diagram of 206Pb/ 208Pb Vs 207Pb/ 208Pb they would produce a single line, the slope of which yields the age as is conventionally calculated. Thus without measuring the often hopelessly non-correlated U (mostly because of prevalent recent U-Pb mobility), a uranium-enriched mineral (e. g., zircon), may be accurately dated. Furthermore, two other aspects of evolution-history may be revealed: (1) In a case where determination of initial Pb on a Quasi Differential Diagram was possible, the age of the source is calculable in a straightforward fashion from the radiogenic ratio of 207Pb/ 206Pb; (2) Events resulting in coexisting re-equilibrated domains may be resolvable into

  15. Major, trace element and isotope geochemistry (Sr-Nd-Pb) of interplinian magmas from Mt. Somma-Vesuvius (Southern Italy)

    USGS Publications Warehouse

    Somma, R.; Ayuso, R.A.; de Vivo, B.; Rolandi, G.

    2001-01-01

    compositions in the interplinian rocks show a tendency to become slightly more radiogenic with age, from the Protohistoric (143Nd/144Nd=0.51240-0.51247) to Ancient Historic (143Nd/144Nd=0.51245-0.51251). Medieval interplinian activity (143Nd/144Nd: 0.51250-0.51241) lacks meaningful internal trends. All the interplinian rocks have virtually homogeneous compositions of 207Pb/204Pb and 208Pb/204Pb in acid-leached residues (207Pb/204Pb ???15.633 to 15.687, 208Pb/204Pb ???38.947 to 39.181). Values of 206Pb/204Pb are very distinctive, however, and discriminate among the three interplinian cycles of activity (Protohistoric: 18.929-18.971, Ancient Historic: 19.018-19.088, Medieval: 18.964-19.053). Compositional trends of major, trace element and isotopic compositions clearly demonstrate strong temporal variations of the magma types feeding the Somma-Vesuvius activity. These different trends are unlikely to be related only to low pressure evolutionary processes, and reveal variations of parental melt composition. Geochemical data suggest a three component mixing scheme for the interplinian activity. These involve HIMU-type and DMM-type mantle and Calabrian-type lower crust. Interaction between these components has taken place in the source; however, additional quantitative constraints must be acquired in order to better discriminate between magma characteristics inherited from the sources and those acquired during shallow level evolution.

  16. Contrasting zircon morphology and UPb systematics in peralkaline and metaluminous post-orogenic granite complexes of the Arabian Shield, Kingdom of Saudi Arabia

    USGS Publications Warehouse

    Aleinikof, J.N.; Stoeser, D.B.

    1989-01-01

    Uzircon ages are reported for seven metaluminous-to-peralkaline post-orogenic granites from the Late Proterozoic Arabian Shield of Saudi Arabia. Zircons from the metaluminous rocks are prismatic, with length-to-width ratios of ??? 2-4: 1 and small pyramidal terminations. In contrast, zircons from three of the four peralkaline complexes either lack well-developed prismatic faces (are pseudo-octahedral) or are anhedral. Some zircons from the peralkaline granites contain inherited radiogenic Pb and have very high common Pb contents (206Pb/204Pb < 150), making the UPb method poorly suited for determining the age of these rocks. Zircons in the metaluminous granites do not contain inheritance and yield well-defined concordia intercepts. The span of ages of the seven complexes (670-470 Ma) indicates that post-orogenic granitic magmatism was not a singular event in the Arabian Shield but rather occurred as multiple intrusive episodes from the Late Proterozoic to the Middle Ordovician. ?? 1989.

  17. ``Isotope language'' of the Alpine Iceman investigated with AMS and MS

    NASA Astrophysics Data System (ADS)

    Kutschera, Walter; Müller, Wolfgang

    2003-05-01

    This paper reviews the use of stable and radioactive isotopes to elucidate an extraordinary archaeological find, the Alpine Iceman "Ötzi". In 1991 the body of this man was accidentally discovered in an ice-filled depression at a high-altitude mountain pass (Tisenjoch, 3210 m) of the Ötztal Alps. This location at the Austrian-Italian border apparently formed an ancient transition across the Alps from South to North. 14C dating of the body with accelerator mass spectrometry (AMS) revealed that the Iceman had lived some 5200 years ago, within the time period from 3370 to 3100 years BC (Before Christ). A variety of other materials from the discovery site were also dated with 14C AMS suggesting a use of the mountain pass at other time periods, and varying climatic conditions. Ongoing investigations with thermal ionization (TIMS), inductively-coupled plasma (ICP-MS) and gas mass spectrometry include isotope ratios of 18O/ 16O ( δ18O), 87Sr/ 86Sr and 206Pb/ 204Pb, in order to reveal the Iceman's origin and migrational behavior. Analyzed samples include tooth enamel, bones and contents of his intestine, which all represent different ontogenetic (developmental) stages. The isotopic composition of the Iceman is compared to both soils from archaeological sites and local waters. Taken together, the results point towards an origin of the Iceman in the Southeast of the finding site, consistent with archaeological and paleobotanical data.

  18. High-precision UPb ages of metamorphic rutile: application to the cooling history of high-grade terranes

    USGS Publications Warehouse

    Mezger, K.; Hanson, G.N.; Bohlen, S.R.

    1989-01-01

    Metamorphic rutiles occurring in granulite and upper amphibolite facies metapelitic rocks of the Archean Pikwitonei granulite domain (Manitoba) and the Proterozoic Adirondack terrane (New York) give concordant and near concordant UPb ages. The Pb concentrations in rutile range from 2.85 to 168 ppm, U concentrations range from 10.9 to 390 ppm and the measured 206Pb 204Pb ratios range from 182 to 22,100 corresponding to 238U 204Pb ratios of 398-75,100. The proportions of radiogenic 208Pb are very low, ranging from 0.0 to 6.9% of total radiogenic Pb. The habits of the rutile crystals range from stubby to acicular, the physical properties vary from opaque/black to transparent/reddish-brown. Separate batches of black and reddish-brown rutile grains from the same samples have similar U and Pb concentrations, Pb-isotope ratios, and yield the same U Pb ages within analytical uncertainty. No correlation of U concentration and 206Pb 204Pb ratios with morphology or color of the rutiles was observed among the samples analyzed. Most rutiles yield concordant UPb ages which are reproducible within analytical uncertainty, i.e. generally ??2 Ma. The UPb ages for prograde rutile are younger than the time of peak metamorphism given by UPb ages for garnet and zircon, and also younger than UPb ages for sphene and monazite, and 40Ar 39Ar and KAr ages for hornblende but older than 40Ar 39Ar and KAr ages for biotite from the same area. This suggests that the rutile ages reflect cooling below closure temperatures. Within a single hand-specimen, and thus for an identical thermal history, larger rutile grains give older ages than do smaller grains. This suggests that volume diffusion is the most probable mechanism responsible for the ages being younger than the time of peak metamorphism. It also suggests that the dimensions for such diffusion are directly related to the dimensions of the rutile crystal and not to the dimensions of sub-grain domains, as is the case for Ar diffusion in

  19. The geochemical fingerprint of serpentinite- and crust-dominated plate-interface settings: some tectonic implications

    NASA Astrophysics Data System (ADS)

    Cannaò, Enrico; Scambelluri, Marco; Agostini, Samuele; Tonarini, Sonia

    2014-05-01

    The interface between converging plates is made of kilometre-thick domains where slab and upper plate mantle materials are tectonically slicied within a matrix dominated either by (meta)sedimentary/crustal rocks or by serpentinite. The latter may correspond to supra-subduction mantle altered by uprising slab fluids. Once formed, these plate-interface domains act as hydrated low-viscosity layers where tectonic stress and fluid-mediated mass transfer are strongly focussed. Here we present the geochemical study of two plate-interface environments: (1) serpentinite-rich, represented by the high-pressure serpentinites of the Ligurian Alps (Erro-Tobbio and Voltri Units); (2) sediment-dominated top slab mélange, represented by de-serpentinized garnet peridotite and chlorite harzburgite bodies (hosting eclogite and metarodingite) embedded in paragneiss and micaschist from Cima di Gagnone (Adula Unit, Central Alps). The Ligurian serpentinites derive from oceanic and wedge mantle tectonically coupled and dragged to depth during Alpine subduction: they may represent the hydrated precursors of the Cima di Gagnone peridotites. The B, Pb and Sr isotopic composition of the above sets of rocks helps defining tectonic and mass transfer processes during accretion of slab and suprasubduction mantle rocks in plate-interface domains, and to retrieve the imprint of fluids from these settings, which that ultimately affect arc magmatism. The serpentinized peridotites from Erro-Tobbio (ET) show high B (10-30 ppm), delta11B (10-25 per mil), B/Nb ratio (>380) and limited enrichment in 206Pb/204Pb (18.17-18,51) and 87Sr/86Sr (0.7046- 0.7060). Scambelluri & Tonarini (2012) interpreted the B and Sr isotopic imprint of ET as representative of upper plate mantle altered by slab-fluids. The B contents (up to 30 ppm), delta11B (18-30 per mil), B/Nb ratio (>900) and 206Pb/204Pb (18.09-18.22) of the Voltri serpentinites are similar to ET. Their 87Sr/86Sr (0.7079 to 0.7105) is higher than ET. The

  20. Isotope evolution in the HIMU reservoir beneath St. Helena: Implications for the mantle recycling of U and Th

    NASA Astrophysics Data System (ADS)

    Hanyu, Takeshi; Kawabata, Hiroshi; Tatsumi, Yoshiyuki; Kimura, Jun-Ichi; Hyodo, Hironobu; Sato, Keiko; Miyazaki, Takashi; Chang, Qing; Hirahara, Yuka; Takahashi, Toshiro; Senda, Ryoko; Nakai, Shun'ichi

    2014-10-01

    HIMU (high-μ; 238U/204Pb) is a mantle reservoir that has been thought to form by subduction and subsequent storage of ancient oceanic crust and lithosphere in the mantle. In order to constrain the processes that acted on subducted materials over several billion years, we present precise Pb-Sr-Nd-Hf-He isotopic data together with 40Ar/39Ar and K/Ar ages of HIMU lavas from St. Helena in the Atlantic. Clinopyroxene separates were analyzed together with whole-rock samples to better describe the geochemical characteristics of the HIMU component. Although isotopic variations are small in the St. Helena lavas (20.6-21.0 for 206Pb/204Pb) between 12 and 8 Ma, the younger lavas have more HIMU-like isotopic compositions than the older lavas. The mixing arrays defined by these lavas are remarkably similar to those observed in HIMU lavas from Austral Islands in the Pacific, suggesting that the two HIMU reservoirs located in different mantle domains are characterized by similar isotopic compositions with radiogenic 206Pb/204Pb and 208Pb/204Pb, enriched Nd and Hf isotopes, depleted Sr isotopes, and radiogenic 3He/4He. However, there is a significant difference between the St. Helena and Austral Islands lavas in 207Pb/204Pb. The St. Helena lavas show systematically higher 207Pb/204Pb for a given 206Pb/204Pb. Lead isotope evolution models suggest that both HIMU reservoirs formed around 2 Ga; however, the HIMU reservoir for St. Helena is about 0.3 Ga older than that for Austral Islands. The relation between 206Pb/204Pb and 208Pb/204Pb could reflect the time-integrated κ (232Th/238U) in the components. The HIMU components for St. Helena and Austral Islands have κ values between 3.3 and 3.7, which are intermediate between the present-day fresh mid-ocean ridge basalts (MORB; 2.6-3.2) and the chondritic silicate Earth (∼4). This is consistent with the model that the HIMU precursor is subducted oceanic crust created around 2 Ga from depleted upper mantle, in which κ monotonously

  1. Melt-generation processes associated with the Tristan mantle plume: Constraints on the origin of EM-1

    NASA Astrophysics Data System (ADS)

    Gibson, S. A.; Thompson, R. N.; Day, J. A.; Humphris, S. E.; Dickin, A. P.

    2005-09-01

    that, at the time of continental break-up, this would have been located above the sites of subsequent EM-1 melt generation. Shallow-mantle recycling of metasomatised lithosphere delaminated from south-west Africa and south-east Brazil may explain the further variations in trace-element and isotopic ratios of 100 and 80 to 30 Ma basalts from the Walvis Ridge, respectively. Recent magmas from Tristan, Inaccessible and Gough contain a melt contribution from an enriched mantle source with high 206Pb / 204Pb, 208Pb / 204Pb and 87Sr / 86Sr ratios and low ɛNd, relative to bulk-Earth. This does not resemble the isotopic composition of mafic-potassic magmas from continents adjacent to the South Atlantic and we therefore propose that it is a deep-recycled mantle component. The high Pb-isotopic ratios of recent Tristan plume magmas are inconsistent with a melt contribution from recycled oceanic crust plus a few percent pelagic sediments. We suggest that the deep mantle component is recycled metasomatised lithospheric mantle. Recycled metasomatised lithospheric mantle, of variable composition, only appears to have been an intrinsic part of the sub-oceanic Tristan mantle plume and the bulk-rock composition of present-day Tristan plume related melts are therefore inappropriate for modelling the contribution of plume-derived melts to the Paraná-Etendeka continental flood-basalts. This relationship may also apply to other large igneous provinces and ocean islands along their associated hot spot tracks.

  2. Mafic dykes intrusive into Pre-Cambrian rocks of the São Luís cratonic fragment and Gurupi Belt (Parnaíba Province), north-northeastern Brazil: Geochemistry, Sr-Nd-Pb-O isotopes, 40Ar/39Ar geochronology, and relationships to CAMP magmatism

    NASA Astrophysics Data System (ADS)

    Klein, Evandro L.; Angélica, Rômulo S.; Harris, Chris; Jourdan, Fred; Babinski, Marly

    2013-07-01

    Dykes of diabase and microgabbro intruded into Pre-Cambrian rocks of the São Luís cratonic fragment and Gurupi Belt, which are tectonic and erosive windows of the Parnaíba Basin in north-northeastern Brazil. Ar-Ar ages were determined, and major, trace element, and Nd-Sr-Pb-O isotopic compositions of these dykes were measured to provide insights into their age, and into the nature of their mantle sources and petrogenetic processes. The data have also been used to compare the chemical and isotopic signatures of the dykes with those of the Central Atlantic Magmatic Province (CAMP). Four chemical groups of mafic dykes have been identified. These comprise two subtypes of high-Ti rocks (i) HTi-1 (TiO2 < 2.3 wt.%; SiO2 > 47 wt.%), (ii) HTi-2 (TiO2 > 2.7 wt.%; SiO2 > 47 wt.%), in addition to (iii) evolved high-Ti (TiO2 > 4 wt.%; SiO2 of ~ 46 wt.%) and (iv) low-Si (TiO2 > 2.2 wt.%; SiO2 < 45 wt.%) rocks. 40Ar/39Ar geochronology of plagioclase returned ages of 201 ± 4 Ma and 193 ± 10 Ma for the HTi-2 subtype, and of 201 ± 2 Ma and 207 ± 9 Ma for the evolved high-Ti group. The HTi-1 and low-Si groups presented highly disturbed age spectra, and did not allow the definition of their emplacement ages. The Argon data indicate an age > 200 Ma for the low-Si group and are dubious with respect to the age of theHTi-1 subtype, if coeval with (i.e., ~ 200 Ma), or older than, the HTi-2 and evolved high-Ti types. All groups present δ18O values of pyroxene that are compatible with uncontaminated mantle-derived magmas. The HTi-1 subtype (average 143Nd/144Nd200 = 0.512644; 87Sr/86Sr200 = 0.7035; 206Pb/204Pb of 17.86) shows the less enriched and less fractionated (more primitive) trace element distribution of all groups. The HTi-2 subtype shows enriched trace element pattern and depleted Nd-Sr signature (143Nd/144Nd200 = 0.512610; 87Sr/86Sr200 = 0.7037) and average 206Pb/204Pb ratios of 17.23. The evolved high-Ti chemical group shows average ratios of 143Nd/144Nd200 = 0.512558, 87Sr

  3. Geochemistry of Garibaldi Lake andesites and dacites indicates crustal contamination involved in formation of Northern Cascade arc lavas

    NASA Astrophysics Data System (ADS)

    Martindale, M.; Mullen, E.; Weis, D.

    2013-12-01

    The Cascade Arc presents a unique setting for studying the controls on andesite genesis and the implications for growth and evolution of the continental crust. It is the type-locality for a ';hot' subduction zone, where the downgoing slab is young and subduction is relatively slow. The northern segment of the Cascade arc, the Garibaldi Volcanic Belt (GVB), hosts the youngest subducting crust in Cascadia and the termination of the subducting slab. These conditions may affect magma generation processes by reducing the amount of water reaching the area of melt generation [1,2] and imparting an adakitic signature to magmas generated there if the slab edge melts [3]. We provide insights on the origin of andesites and dacites from the Garibaldi Lake area using new high-precision Pb, Sr, Nd, Hf isotope ratios and trace element data. Andesites and dacites from the Garibaldi Lake area (The Black Tusk, Mt. Price, and The Table) are calc-alkaline and show evidence for crustal contamination such as positive correlations between Ba/Nb and SiO2. Silica variation diagrams show no systematic trend for any of the volcanic centres, suggesting the presence of distinct magma batches. Garibaldi Lake andesites and dacites have among the least radiogenic Pb isotope ratios of all Cascade arc lavas, and define a linear array in Pb-isotope space. This most likely reflects mixing between MORB-source mantle (similar to Gorda and Explorer plate sources) and locally subducting sediments [4]. However, relative to GVB basalts and lavas from the rest of the Cascades (High Cascades), the andesites and dacites have higher 207Pb/204Pb (15.55-15.56) for a given 206Pb/204Pb (18.66-18.74). The Garibaldi Lake lavas also have higher 87Sr/86Sr (0.7033-0.7036) and lower ɛNd (5.8-7.9) at a given 206Pb/204Pb than GVB basalts and High Cascades lavas but among the highest ɛNd for a given SiO2 for the whole of the Cascades. ɛHf values (10.5-13.5) are higher at a given SiO2 value for Garibaldi Lake evolved

  4. The fate of atmospherically derived Pb in Central European catchments: insights from spatial and temporal pollution gradients and Pb isotope ratios.

    PubMed

    Bohdalkova, Leona; Novak, Martin; Stepanova, Marketa; Fottova, Daniela; Chrastny, Vladislav; Mikova, Jitka; Kubena, Ales A

    2014-04-15

    Soils in polluted regions are generally regarded as a delayed, long-lasting source for Pb contamination of aquatic systems. Lead deposited on topsoil is slowly transported downward with particulate and colloidal organic matter, driven by infiltrating precipitation. Then, Pb is tightly retained in mineral soil. Lead export from catchments is extremely low and decoupled from the atmospheric input. We tested this hypothesis in 11 small catchments, differing in pollution levels. Input/ouput Pb fluxes were monitored for 14-15 years in an era of decreasing industrial Pb emission rates. Between 1996/1997 and 2010, Pb deposition fluxes decreased significantly, on average by 80%. At the beginning of the monitoring, Pb export constituted 2 to 58% of Pb input. At the end of the monitoring, Pb export constituted 2 to 95% of Pb input. Highly polluted sites in the northeast exported significantly more Pb than less polluted sites further south. The (206)Pb/(207)Pb isotope ratios of runoff (1.16) were identical to those of topsoil and present-day deposition, and different from mineral soil and bedrock. Lead isotope systematics and between-site flux comparisons indicated that a portion of the incoming Pb had a relatively short residence time in the catchments, on the order of decades.

  5. Using S and Pb isotope ratios to trace leaching of toxic substances from an acid-impacted industrial-waste landfill (Pozdatky, Czech Republic).

    PubMed

    Novak, Martin; Pacherova, Petra; Erbanova, Lucie; Veron, Alain J; Buzek, Frantisek; Jackova, Ivana; Paces, Tomas; Rukavickova, Lenka; Blaha, Vladimir; Holecek, Jan

    2012-10-15

    Slightly elevated concentrations of toxic species in waters sampled in the surroundings of a leaky landfill may be both a sign of an approaching contaminant plume, or a result of water-rock interaction. Isotopes can be instrumental in distinguishing between anthropogenic and geogenic species in groundwater. We studied sulfur and lead isotope ratios at an abandoned industrial-waste landfill, located in a densely populated part of Central Europe. Stable isotope variability in space and time was used to follow the movement of a groundwater plume, contaminated with toxic metals (Cd, Cr, Be), in fractured granitoids. Toxic metals had been mobilized from industrial waste by a strong pulse of sulfuric acid, also deposited in the landfill. Both tracers exhibited a wide range of values (δ(34)S between +2.6 and +18.9‰; (206)Pb/(207)Pb between 1.16 and 1.39), which facilitated identification of mixing end-members, and made it possible to assess the sources of the studied species. In situ fractionations did not hinder source apportionment. Influx of contaminated groundwater was observed neither in irrigation wells in a nearby village, nor at distances greater than 300 m from the landfill. Combination of stable isotope tracers can be used as part of an early-warning system in landscapes affected by landfills.

  6. Early Cretaceous continental delamination in the Yangtze Block: Evidence from high-Mg adakitic intrusions along the Tanlu fault, central Eastern China

    NASA Astrophysics Data System (ADS)

    Jia, Liqiong; Mo, Xuanxue; Santosh, M.; Yang, Zhusen; Yang, Dan; Dong, Guochen; Wang, Liang; Wang, Xinchun; Wu, Xuan

    2016-09-01

    Early Cretaceous high-Mg adakitic rocks from central Eastern China provide important insights into the thinning mechanism of the over-thickened lithosphere in the Yangtze Block (YB) as well as the North China Block (NCB). The Tanlu fault (TLF), located between the North China and Yangtze Blocks, and has been considered as a prominent pathway of magmas and fluids that resulted in lithosphere thinning of the YB during the Mesozoic-Cenozoic. Here we report the petrology, whole-rock geochemistry, zircon U-Pb geochronology, in situ Hf isotopes, and whole-rock Sr-Nd-Pb isotopes of four high-Mg adakitic intrusions along the TLF in northeastern Langdai. These adakitic intrusions consist of monzodiorite, quartz monzonite porphyry, and quartz monzodiorite. Zircon LA-MC-ICPMS analyses of five samples yield weighted mean 206Pb/238U ages of 127.58 ± 0.80, 126.90 ± 0.81, 120.71 ± 0.64, 122.75 ± 0.57, and 129.2 ± 1.1 Ma, indicating their emplacement during the Early Cretaceous. The intrusions have intermediate SiO2 (53.18-65.48 wt%) and high potassium (K2O = 3.07-3.95 wt%; Na2O/K2O = 1.02-1.26) and are classified as shoshonitic to high-K calc-alkaline series. They are characterized by high MgO (1.80-7.35 wt%), Mg# (50-65), Sr (591-1183 ppm), Ni (20.3-143.0 ppm), and Cr (51.40-390.0 ppm) contents, high (La/Yb)N (11.60-28.33) and Sr/Y (27.9-113.5) ratios, and low Y (7.79-22.4 ppm) and Yb (0.60-2.01 ppm) contents, comparable with high-Mg adakites. The samples are enriched in light rare earth elements but depleted in heavy rare earth elements and high field strength elements with slightly negative to positive Eu anomalies (δEu = 0.81-1.30), resembling the features of high-Mg adakitic rocks. Their whole-rock εNd(t) = -16.2 to -15.0, initial (87Sr/86Sr)i = 0.7060-0.7074, low radiogenic Pb (206Pb/204Pb(t) = 16.208-16.509, 207Pb/204Pb(t) = 15.331-15.410, and 208Pb/204Pb(t) = 36.551-36.992), and zircon εHf(t) = -36.6 to -16.6 suggest magma derivation from a continental crustal

  7. The isotopic and chemical evolution of Mount St. Helens

    USGS Publications Warehouse

    Halliday, A.N.; Fallick, A.E.; Dickin, A.P.; Mackenzie, A.B.; Stephens, W.E.; Hildreth, W.

    1983-01-01

    Isotopic and major and trace element analysis of nine samples of eruptive products spanning the history of the Mt. St. Helens volcano suggest three different episodes; (1) 40,000-2500 years ago: eruptions of dacite with ??{lunate}Nd = +5, ??{lunate}Sr = -10, variable ??18O, 206Pb/204Pb ??? 18.76, Ca/Sr ??? 60, Rb/Ba ??? 0.1, La/Yb ??? 18, (2) 2500-1000 years ago: eruptions of basalt, andesite and dacite with ??{lunate}Nd = +4 to +8, ??{lunate}Sr = -7 to -22, variable ??18O (thought to represent melting of differing mantle-crust reservoirs), 206Pb/204Pb = 18.81-18.87, variable Ca/Sr, Rb/Ba, La/Yb and high Zr, (3) 1000 years ago to present day: eruptions of andesite and dacite with ??{lunate}Nd = +6, ??{lunate}Sr = -13, ??18O ???6???, variable 206Pb/204Pb, Ca/Sr ??? 77, Rb/Ba = 0.1, La/Yb ??? 11. None of the products exhibit Eu anomalies and all are LREE enriched. There is a strong correlation between 87Sr/86Sr and differentiation indices. These data are interpreted in terms of a mantle heat source melting young crust bearing zircon and garnet, but not feldspar, followed by intrusion of this crustal reservoir by mantle-derived magma which caused further crustal melting and contaminated the crustal magma system with mafic components. Since 1000 years ago all the eruptions have been from the same reservoir which has displayed a much more gradual re-equilibration of Pb isotopic compositions than other components suggesting that Pb is being transported via a fluid phase. The Nd and Sr isotopic compositions lie along the mantle array and suggest that the mantle underneath Mt. St. Helens is not as depleted as MORB sources. There is no indication of seawater involvement in the source region. ?? 1983.

  8. Sulfate-water isotope geothermometry and lead isotope data for the regional geothermal system in the Twin Falls Area, South-Central Idaho

    SciTech Connect

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

    1997-12-31

    Sulfate-water isotope geothermometry for the geothermal system at Twin Falls, Idaho indicates aquifer-temperatures of 90{degrees} to 106{degrees}C; most sites are between 90{degrees} and 93{degrees}C. {sup 206}Pb/{sup 204}Pb and {sup 208}Pb/{sup 204}Pb 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.

  9. Louisville seamount subduction and its implication on mantle flow beneath the central Tonga-Kermadec arc.

    PubMed

    Timm, Christian; Bassett, Daniel; Graham, Ian J; Leybourne, Matthew I; de Ronde, Cornel E J; Woodhead, Jon; Layton-Matthews, Daniel; Watts, Anthony B

    2013-01-01

    Subduction of intraplate seamounts beneath a geochemically depleted mantle wedge provides a seldom opportunity to trace element recycling and mantle flow in subduction zones. Here we present trace element and Sr, Nd and Pb isotopic compositions of lavas from the central Tonga-Kermadec arc, west of the contemporary Louisville-Tonga trench intersection, to provide new insights into the effects of Louisville seamount subduction. Elevated (206)Pb/(204)Pb, (208)Pb/(204)Pb, (86)Sr/(87)Sr in lavas from the central Tonga-Kermadec arc front are consistent with localized input of subducted alkaline Louisville material (lavas and volcaniclastics) into sub-arc partial melts. Furthermore, absolute Pacific Plate motion models indicate an anticlockwise rotation in the subducted Louisville seamount chain that, combined with estimates of the timing of fluid release from the subducting slab, suggests primarily trench-normal mantle flow beneath the central Tonga-Kermadec arc system. PMID:23591887

  10. Louisville seamount subduction and its implication on mantle flow beneath the central Tonga-Kermadec arc.

    PubMed

    Timm, Christian; Bassett, Daniel; Graham, Ian J; Leybourne, Matthew I; de Ronde, Cornel E J; Woodhead, Jon; Layton-Matthews, Daniel; Watts, Anthony B

    2013-01-01

    Subduction of intraplate seamounts beneath a geochemically depleted mantle wedge provides a seldom opportunity to trace element recycling and mantle flow in subduction zones. Here we present trace element and Sr, Nd and Pb isotopic compositions of lavas from the central Tonga-Kermadec arc, west of the contemporary Louisville-Tonga trench intersection, to provide new insights into the effects of Louisville seamount subduction. Elevated (206)Pb/(204)Pb, (208)Pb/(204)Pb, (86)Sr/(87)Sr in lavas from the central Tonga-Kermadec arc front are consistent with localized input of subducted alkaline Louisville material (lavas and volcaniclastics) into sub-arc partial melts. Furthermore, absolute Pacific Plate motion models indicate an anticlockwise rotation in the subducted Louisville seamount chain that, combined with estimates of the timing of fluid release from the subducting slab, suggests primarily trench-normal mantle flow beneath the central Tonga-Kermadec arc system.

  11. Direct ion microprobe U-Pb dating of fossil tooth of a Permian shark

    NASA Astrophysics Data System (ADS)

    Sano, Yuji; Terada, Kentaro

    1999-12-01

    We report here direct ion microprobe dating of fossil tooth (dentine) of a Permian fresh-water shark, Orthacanthus senckenbergianus using the SHRIMP instrument recently installed at Hiroshima University. Fifteen spots on the small sample (approximately 2 mm×1 mm) indicate a 238U/ 206Pb isochron age of 266±18 Ma and a Tera-Wasserburg concordia intercept age of 266±24 Ma in a three-dimensional 238U/ 206Pb- 207Pb/ 206Pb- 204Pb/ 206Pb diagram. These Permian ages are consistent with a 235U/ 207Pb age of 453±170 Ma and a 232Th- 208Pb age of 235±310 Ma, suggesting indistinguishable depositional and early diagenetic ages of the fossil in its sedimentary sequences. The success of the method depends on the chemical fractionation of uranium from lead in a specimen a few hundred microns in size and the consequent variations in lead isotopic compositions due to radioactive decay.

  12. Direct dating of hydrothermal W mineralization: U-Pb age for hübnerite (MnWO 4), Sweet Home Mine, Colorado

    NASA Astrophysics Data System (ADS)

    Romer, Rolf L.; Lüders, Volker

    2006-09-01

    We have investigated the potential of hübnerite for U-Pb dating. Hübnerite forms typically at medium to low-temperatures in a wide range of pneumatolytic-hydrothermal mineral deposits, particularly porphyry molybdenum and Sn-specialized granites. Hübnerite from the Sweet Home Mine (Alma, Colorado) formed in a Pb-rich, U-poor environment, but still developed relatively radiogenic Pb isotopic compositions. The low Pb common contents in hübnerite (0.075 to 0.155 ppm) demonstrate that Pb is efficiently excluded from the crystal lattice. In contrast, U may substitute for Mn. The U-Pb data of hübnerite scatter. Most of the scatter originates from samples with 206Pb/ 204Pb values below 50, where Pb blank contributes up to 30% to Pb total. Using the least radiogenic galena Pb, samples with 206Pb/ 204Pb values above 70 have overlapping 206Pb∗/ 238U and 207Pb∗/ 235U values and yield a 206Pb/ 238U age of 25.7 ± 0.3 Ma (2σ). Late stage apatite from the Sweet Home Mine yields a 206Pb/ 204Pb- 238U/ 204Pb isochron corresponding to an age of 24.8 ± 0.5 Ma (2σ). A comparison of the U-Pb hübnerite ages with literature 40Ar/ 39Ar ages on earlier sericite and the U-Pb age on later apatite suggests that (i) hübnerite yields accurate U-Pb ages and (ii) the evolution of the Sweet Home mineralization from greisen-type mineralization to medium-temperature hydrothermal vein mineralization took place in a few hundred thousand years at most. Aqueous low-N 2-bearing and aqueous inclusions in the dated hübnerite have homogenization temperatures between 325 and 356 °C and moderate salinity (up to 6.7 wt% NaCl equiv.). Thus, hübnerite represents one of the rare examples of a mineral that can be dated accurately and carries petrological information.

  13. Minerals as mantle fingerprints: Sr-Nd-Pb-Hf in clinopyroxene and He in olivine distinguish an unusual ancient mantle lithosphere beneath the East African Rift System

    NASA Astrophysics Data System (ADS)

    Nelson, W. R.; Shirey, S. B.; Graham, D. W.

    2011-12-01

    The East African Rift System is a complex region that holds keys to understanding the fundamental geodynamics of continental break-up. In this region, the volcanic record preserves over 30 Myrs of geochemical variability associated with the interplay between shallow and deep asthenospheric sources, continental lithospheric mantle, and continental crust. One fundamental question that is still subject to debate concerns the relationship between the lithospheric mantle and the voluminous flood basalt province that erupted at ~30 Ma in Ethiopia and Yemen. Whole-rock Re-Os isotopic data demonstrate the high-Ti (HT2) flood basalts (187Os/188Ost = 0.1247-0.1329) and peridotite xenoliths (187Os/188Ost = 0.1235-0.1377) from NW Ethiopia have similar isotopic compositions. However, Sr-Nd-Pb-Hf isotopic signatures from peridotite clinopyroxene grains are different from those of the flood basalts. The peridotite clinopyroxene separates bear isotopic affinities to anciently depleted mantle (87Sr/86Sr = 0.7019-0.7029; ɛNd = 12.6-18.5; ɛHf = 13.8-27.6) - more depleted than the MORB source - rather than to the OIB-like 30 Ma flood basalts (87Sr/86Sr ~ 0.704; ɛNd = 4.7-6.7; ɛHf = 12.1-13.5). Peridotite clinopyroxenes display two groups of 206Pb/204Pb compositions: the higher 206Pb/204Pb group (18.7-19.3) is compositionally similar to the flood basalts (206Pb/204Pb = 18.97-19.02) whereas the lower 206Pb/204Pb group (17.1-17.9) overlaps with depleted mantle. This suggests that the Pb isotope systematics in some of the peridotites have been metasomatically perturbed. Helium isotopes were analyzed by crushing olivine separated from the peridotites and the flood basalts. Olivine in the peridotites has low He concentrations (0.78-4.7 ncc/g) and low 3He/4He (4.6-6.6 RA), demonstrating that they cannot be the petrogenetic precursor to the high 3He/4He (>12 RA) flood basalts. Notably, these peridotites have 3He/4He signatures consistent with a lithospheric mantle source. Therefore

  14. A new interpretive procedure for whole rock U-Pb Systems applied to the Vredefort crustal profile

    NASA Astrophysics Data System (ADS)

    Welke, H.; Nicolaysen, L. O.

    1981-11-01

    Granulite grade Precambrian gneisses have usually undergone at least one period of strong U depletion. Whole rock U-Pb isotope studies can determine the time(s) of the severe depletion, and this work attempts to place such studies on a more rigorous footing. Two-stage U-Pb systems can be described in terms of one major, episodic differentiation into rocks with varying U/Pb ratios, while three-stage systems can be described by two such distinct episodes. Most of the Precambrian granulites that have been isotopically analyzed have histories too complex to be described as two-stage systems. However, it is demonstrated here that U-Pb data on whole rock suites can yield the complete U-Pb chemical history of a three-stage system (in terms of U/Pb ratios). For a suite of granulites, present-day 207Pb/204Pb and 206Pb/204Pb ratios and element concentration data allow these ratios to be calculated at a number of specific past times and plotted as an array. The degree of scatter in each of these `past arrays' is graphed as a function of time. The point of least scatter denotes the age of the end of stage 2 in the history of the system. The array slope and the dating of the end of stage 2 also permit the beginning of stage 2 to be calculated. All other parameters in the system (U and Pb concentrations, Pb isotopic ratios) can now be determined for each individual rock throughout its history. The new interpretive method also distinguishes sensitively among various kinds of uranium fractionation which may have operated during the differentiation episodes. It is applied here to uranium-depleted granulites in the deeper part of the Vredefort crustal profile. The times of the two fractionating episodes are calculated at ˜3860 and ˜2760 m.y., respectively. The Vredefort 3070 m.y. event, when geochemical systems in the upper half of the crystalline basement became permanently closed, evidently had little significance for the lower half of the crystalline basement. Some fundamental

  15. Geochemical and isotopic composition of Pan-African metabasalts from southwestern Gondwana: Evidence of Cretaceous South Atlantic opening along a Neoproterozoic back-arc

    NASA Astrophysics Data System (ADS)

    Will, Thomas M.; Frimmel, Hartwig E.; Gaucher, Claudio; Bossi, Jorge

    2014-08-01

    A lithogeochemical and Sr-Nd-Pb isotope study of former oceanic crustal rocks from the Cuchilla Dionisio Terrane in the southern Dom Feliciano Belt, Uruguay (La Tuna amphibolites) and metabasites in the Chameis Subterrane of the Marmora Terrane in the Gariep Belt, Namibia/South Africa shows that these rocks are compositionally very similar and probably represent the same unit on opposite sides of the modern South Atlantic. The mafic rocks from both terranes are tholeiitic metabasalts and -andesites and have depleted rare earth element patterns, generally low TiO2 (< 1.5 wt.%), very low Th/Nb ratios and lack negative Nb-Ta anomalies, all features that are typical of ‘normal' mid-ocean ridge basalts (N-MORB) and/or back-arc basin basalts (BABB). In addition, both rock suites have extremely depleted Nd isotope compositions (εNd630 Ma = 6.7-9.4), superchondritic 147Sm/144Nd ratios, and low 206Pb/204Pb and 207Pb/204Pb initial ratios. The 87Sr/86Sr initial ratios of the La Tuna mafic rocks are low, whereas the Chameis metagabbro samples have higher, possibly alteration-related ratios. The geochemical and isotopic signatures are consistent with the formation of both rock suites in the same mature Neoproterozoic back-arc basin (Marmora Basin), supporting conclusions drawn from earlier provenance studies of metasedimentary units from these terranes. Other mafic rocks from the Marmora Terrane are interpreted as ocean island basalts that formed in a within-plate setting. A corollary of the conclusion that the mafic rocks in the Cuchilla Dionisio and Marmora Terranes formed in the same back-arc basin is (1) that the main Pan-African suture between the Río de la Plata Craton and the Kalahari Craton lies to the west of the Dom Feliciano Belt in South America, and (2) that the opening of the modern South Atlantic did not occur along that suture but along the axis of the Neoproterozoic Marmora back-arc basin.

  16. The Quaternary adakite distribution of Kyushu Island, Ryukyu Arc, Japan

    NASA Astrophysics Data System (ADS)

    Shibata, T.; Yoshikawa, M.; Takemura, K.

    2011-12-01

    The Quaternary volcanoes are widely distributed in Kyusu Island, Japan. Philippine Sea plate is subducting beneath Kyushu. Clear distribution of deep seismic foci is observed below the Quaternary volcanoes in southern area, but not in northern area. Notsu et al. (1990, JVGR) examined the contribution of subduction to the magma source, and emphasized that no slab derived material is observed in northern area from Sr isotopic compositions. Volcanic activity similar to the within-plate type volcanism has been also emphasized for the magma genesis of this area (e.g. Kita et al, 2001, JVGR). However, we found adakitic rocks, which show high Sr/Y ratios and low Y concentrations (e.g. Defant and Drummond, 1990, Nature) from some Quaternary volcanoes in north Kyushu on the basis of published data (Otha et al, 1990, GANKO; Itoh, 1990, GANKO). Therefore, the magma genesis is still controversial. We studied lateral variations of Sr, Nd and Pb isotopic and trace element compositions for Quaternary volcanics from Kyushu to investigate the magma genesis. From the results, a clear variation of Sr/Y ratio, decreasing from north to south, is observed along the volcanic front. Some of the Sr/Y ratio of the most northern part of Kyusu shows the value >100. The all analyzed Pb isotope compositions show a single liner trend in 208Pb/204Pb v.s. 206Pb/204Pb diagram. The liner trend of Pb isotope ratios can be explained by the binary mixing of the Shikoku Basin basalt and tereginious sediment which might be a constituent of the subducting slab. The similar binary mixing relationships are found in Sr and Nd isotopic systematics. The isotopic characteristics of the Quaternary magma in Kyushu can be explained by the magma generation process of island arc, in spite of the lack of deep seismic foci in northern area. It is considered that high and low Sr/Y ratios suggest the contributions of partial melt in the north and aqueous fluid derived from subducting slab in the south, respectively. If

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

    PubMed

    Hosono, Takahiro; Alvarez, Kelly; Kuwae, Michinobu

    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 (210)Pb constant rate of supply model and (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 (206)Pb/(207)Pb and (208)Pb/(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 100years. 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. PMID:27058126

  18. Multispectroscopic and Isotopic Ratio Analysis To Characterize the Inorganic Binder Used on Pompeian Pink and Purple Lake Pigments.

    PubMed

    Marcaida, Iker; Maguregui, Maite; Morillas, Héctor; García-Florentino, Cristina; Knuutinen, Ulla; Carrero, Jose Antonio; Fdez-Ortiz de Vallejuelo, Silvia; Pitarch Martı́, Africa; Castro, Kepa; Madariaga, Juan Manuel

    2016-06-21

    Because of the fact that pigments are not ubiquitous in the archeological record, the application of noninvasive analytical methods is a necessity. In this work, pink and purple lake pigments recovered from the excavations of the ancient city of Pompeii (Campania, Italy) and preserved in their original bowls at the Naples National Archaeological Museum (Italy) were analyzed to characterize the composition of their inorganic binders (mordants). In situ preliminary analyses using a hand-held energy dispersive X-ray fluorescence spectrometer (HH-ED-XRF) allowed us to determine the use of an aluminosilicate enriched in Cu and Pb. Scanning electron microscopy coupled to energy dispersive X-ray spectrometry (SEM-EDS) and benchtop ED-XRF analyses confirmed these results, while inductively coupled plasma mass spectrometry (ICPMS) allowed one to determine the concentration of major, minor, and trace elements. The use of other techniques such as X-ray diffraction (XRD), and micro-Raman and infrared spectroscopies allowed one to characterize the pigments at the molecular level. The high concentration of Cu detected in the pigments (1228-12937 μg g(-1)) could be related to the addition of Cu salts to obtain the desired final hue. The concentrations of Pb (987-2083 μg g(-1)) was also remarkable. Lead isotopic ratio analysis ((206)Pb/(207)Pb) suggested a possible origin related to the leaching of the ancient lead pipes from Pompeii and the subsequent transfer to the buried pigments or to the inorganic binder. Molecular analysis also showed that the binder is composed of an allophane-like clay. Moreover, it was possible to determine that to obtain the final purple hue of a specific pigment, Pompeian blue pigment was also mixed into the dyed clay. PMID:27189380

  19. Lead in the Getchell-Turquoise ridge Carlin-type gold deposits from the perspective of potential igneous and sedimentary rock sources in Northern Nevada: Implications for fluid and metal sources

    USGS Publications Warehouse

    Tosdal, R.M.; Cline, J.S.; Fanning, C.M.; Wooden, J.L.

    2003-01-01

    Lead isotope compositions of bulk mineral samples (fluorite, orpiment, and realgar) determined using conventional techniques and of ore-stage arsenian pyrite using the Sensitive High Resolution Ion-Microprobe (SHRIMP) in the Getchell and Turquoise Ridge Carlin-type gold deposits (Osgood Mountains) require contribution from two different Pb sources. One Pb source dominates the ore stage. It has a limited Pb isotope range characterized by 208Pb/206Pb values of 2.000 to 2.005 and 207Pb/206Pb values of 0.8031 to 0.8075, as recorded by 10-??m-diameter spot SHRIMP analyses of ore-stage arsenian pyrite. These values approximately correspond to 206Pb/204Pb of 19.3 to 19.6, 207Pb/204Pb of 15.65 to 15.75, and 208Pb/204Pb of 39.2 to 39.5. This Pb source is isotopically similar to that in average Neoproterozoic and Cambrian elastic rocks but not to any potential magmatic sources. Whether those clastic rocks provided Pb to the ore fluid cannot be unequivocally proven because their Pb isotope compositions over the same range as in ore-stage arsenian pyrite are similar to those of Ordovician to Devonian siliciclastic and calcareous rocks. The Pb source in the calcareous rocks most likely is largely detrital minerals, since that detritus was derived from the same sources as the detritus in the Neoproterozoic and Cambrian clastic rocks. The second Pb source is characterized by a large range of 206Pb/204Pb values (18-34) with a limited range of 208Pb/204Pb values (38.1-39.5), indicating low but variable Th/U and high and variable U/Pb values. The second Pb source dominates late and postore-stage minerals but is also found in preore sulfide minerals. These Pb isotope characteristics typify Ordovician to Devonian siliciclastic and calcareous rocks around the Carlin trend in northeast Nevada. Petrologically similar rocks host the Getchell and Turquoise Ridge deposits. Lead from the second source was either contributed from the host sedimentary rock sequences or brought into the

  20. Helium isotope geochemistry of some volcanic rocks from Saint Helena

    NASA Astrophysics Data System (ADS)

    Graham, David W.; Humphris, Susan E.; Jenkins, William J.; Kurz, Mark D.

    1992-05-01

    3He/ 4He ratios have been measured for olivine and clinopyroxene phenocrysts in 7-15 m.y. old basaltic lavas from the island of St. Helena. Magmatic helium was effectively resolved from post-eruptive radiogenic helium by employing various extraction techniques, including in vacuo crushing, and stepwise heating or fusion of the powders following crushing. The inherited 3He/ 4He ratio at St. Helena is 4.3-5.9 R A. Helium isotope disequilibrium is present within the phenocrysts, with lower 3He/ 4He upon heating and fusion of the powders following crushing, due to radiogenic ingrowth or to α-particle implantation from the surrounding (U + Th)-rich lavas. A single crushing analysis for clinopyroxene in a basalt from Tubuaii gave 3He/ 4He= 7.1 R A. 3He/ 4He ratios at St. Helena and Tubuaii (HIMU hotspots characterized by radiogenic Pb isotope signatures) are similar to 3He/ 4He ratios previously measured at Tristan da Cunha and Gough Island (EM hotspots characterized by low 206Pb/ 204Pb ). Overall, the He sbnd Sr sbnd Pb isotope systematics at these islands are consistent with a mantle origin as contiguous, heterogeneous materials, such as recycled crust and/or lithosphere. 3He/ 4He ratios at HIMU hotspots are similar to mantle xenoliths which display nearly the entire range of Pb isotope compositions found at ocean islands, and are only slightly less than values found in mid-ocean ridge basalts (7-9 R A). This suggests that the recycled materials were injected into the mantle within the last 10 9 yrs.

  1. Shallow origin for South Atlantic Dupal Anomaly from lower continental crust: Geochemical evidence from the Mid-Atlantic Ridge at 26°S

    NASA Astrophysics Data System (ADS)

    Regelous, Marcel; Niu, Yaoling; Abouchami, Wafa; Castillo, Pat R.

    2009-09-01

    We measured trace element concentrations and Pb isotope compositions of fresh volcanic glass samples from the Mid-Atlantic Ridge at 26°S, and from nearby off-axis seamounts. The samples have previously been studied for major elements and Sr-Nd-He isotopes. All samples are depleted MORB, and include some of the most incompatible trace element depleted lavas yet reported from the Atlantic. The seamount lavas are more depleted in highly incompatible elements than the axial lavas, but have high Sr, Pb and Eu concentrations, relative to REE of similar incompatibility. The lavas with the highest Sr/Nd, Pb/Ce and Eu/Eu* have the highest 3He/4He (up to 11.0 R/RA) ratios and the lowest incompatible trace element concentrations. They also have the highest 87Sr/86Sr (up to 0.7036) and 208Pb/204Pb for a given 206Pb/204Pb ratio, which are characteristics of lavas from the Dupal Anomaly in the South Atlantic, and of many EM-1 type intraplate lavas generally. Our data place constraints on the origin of the Dupal Anomaly. The enrichments in Sr, Pb and Eu, together with the low Ca/Al ratios of the seamount lavas indicate that their mantle source consists of material that at one time contained plagioclase, and must therefore have resided at crustal pressures. We argue that the trace element and isotopic compositions of the seamount lavas are best explained by derivation from a mantle source contaminated with lower continental crust, which was introduced into the upper mantle during continental rifting and breakup in the South Atlantic. Our results support previous suggestions that the Dupal Anomaly in the South Atlantic has a relatively recent, shallow origin in lower continental crust and continental lithospheric mantle, rather than in recycled material supplied from the deeper mantle by plumes. Plate reconstructions place the Parana-Etendeka flood basalt province over the central part of the Dupal Anomaly at the time of rifting of South America and Africa at 134 Ma. The flood

  2. Petrogenesis of the post-collisional Oligo-Miocene Volcanism in NW Anatolia (Turkey): Balıkesir Volcanites

    NASA Astrophysics Data System (ADS)

    Ünal, Alp; Altunkaynak, Şafak; Benowitz, Jeff A.

    2016-04-01

    In this study, we present whole-rock chemical and Sr-Nd-Pb-O isotopic compositions as well as 40Ar/39Ar ages of Balıkesir volcanites to evaluate the nature, genesis and timing of the post-collisional Oligo-Miocene magmatism in NW Anatolia. Three main volcano-stratigraphic groups distinguished in the Balıkesir volcanites on the basis of field observations and petrographical investigations; 1) andesitic lavas and related pyroclastic units representing the lower part of the volcanic sequence; 2) Trachyandesite- basaltic trachyandesite lavas and 3) dacitic lavas and associated pyroclastic units corresponding to the upper part of the volcanic sequence. Both andesitic and dacitic pyroclastic units are represented with ash fall, ash block flow and flow breccia units. Geochemically, Balıkesir volcanites are ranging in composition from basaltic trachy-andesite to dacite. They are sub-alkaline in character and show enrichment in large ion lithophile elements (LILE) and light rare earth elements (LREE) relative to the high field strength elements (HFSE). Balıkesir volcanites display depletion in P, Ta, Nb and Ti. All these trace element characteristics and inter-element ratios suggest that magma forming the Balıkesir volcanites show similar patterns to those of subduction-related arc magmas and/or post collisional lavas. They have high initial 87Sr/86Sr ratios (0.707109-0.708620), low 143Nd/144Nd (0.512322- 0.512493). 206Pb/204Pb and 207Pb/204Pb values vary from 18.703 to 18.867 and 15.681 to 15.714, respectively and ɛNd values range between -5.61 and -2.27. 18O isotopic ratios range between 8.3 and 11.8. All these isotopic characteristics and major-trace element compositions of Balıkesir volcanites suggest that the lavas are co-genetic and originated from a hybrid magma derived from enriched mantle (EM II) source. 40Ar/39Ar dating yielded isochron ages of 22.9±0.2 - 21.0±0.2 which is consistent with other volcanic and plutonic associations of western Anatolia (eg

  3. Eolian inputs of lead to the North Pacific

    SciTech Connect

    Jones, C.E.; Halliday, A.N.; Rea, D.K.; Owen, R.M.

    2000-04-01

    The authors evaluate the importance of natural eolian Pb to the dissolved oceanic Pb budget by measuring the isotopic composition of Pb in 35 Holocene and late Quaternary sediment samples from the North Pacific and in 10 samples of Chinese loess. When the Pacific is divided into sediments provinces based on published {var_epsilon}{sub Nd} and sedimentological data, Pb from the central North Pacific tends to be the most radiogenic and homogeneous due to the dominance of eolian Chinese loess. Lead from the marginal North Pacific and the sparsely sampled regions south of 5{degree}N are less radiogenic and more variable owing to hemipelagic inputs from various volcanic arcs and older continental crust located around the Pacific Rim. {sup 208}Pb/{sup 204}Pb ratios provide the most distinctive provenance information due to the relatively high ratios in Chinese loess. The Chinese loess samples come from 3 localities and span up to 2 Myr of time. Acetic-acid leachate, bulk loess, and loess silicate fractions were analyzed separately. Leachate Pb is considerably less radiogenic than silicate Pb. The isotopic composition of the silicate component closely matches the sediment data from the central North Pacific, confirming the dominance of eolian loess in this region. The authors divided up a suite of published hydrogenous Pb-isotope data from the Pacific Ocean according to their locations within the three independently defined sediment provinces. These data define three distinct fields differentiated primarily by their {sup 206}Pb/{sup 204}Pb ratios, which increase going form the Central to Southern to Marginal provinces. This relationship with sediment province strongly suggests that natural eolian and probably hemipelagic inputs significantly impact the seawater Pb budget. Direct support for the dominance of eolian Chinese loess in the central North Pacific dissolved Pb budget comes from the close match between loess leachate Pb and the Central Province hydrogenous Pb data

  4. Subduction components in Pleistocene to recent Kurile arc magmas in NE Hokkaido, Japan

    NASA Astrophysics Data System (ADS)

    Hoang, Nguyen; Itoh, Jun'ichi; Miyagi, Isoji

    2011-03-01

    Samples of Kurile arc lavas erupted between 1.6 Ma and ca. 30,000 years were collected from the Kutcharo, Mashu and Akan caldera area in NE Hokkaido, about 150 km west of the Kurile trench. The samples include rhyolitic pumice, rhyolite, dacite, andesite and, rare, tholeiitic basalt, and show 'medium' potassic calc-alkaline affinity. Except for relatively high concentrations of large ionic lithophile elements (LILE), Th and especially Pb, other trace elements, including the rare earths (REE) and high field strength elements (HFSE), show relatively low abundances when compared with those of normal mid-ocean ridge basalts (N-MORB). Their Sr, Nd isotopic compositions are relatively depleted, with 87Sr/ 86Sr ranging from 0.7033 to 0.7034 and 143Nd/ 144Nd from 0.51295 to 0.51230. Pb isotopic compositions are also relatively unradiogenic, with 206Pb/ 204Pb at about 18.4 and 208Pb/ 204Pb ranging from 38.3 to 38.4, significantly more depleted than other Quaternary lavas in NE Japan. The Kurile lavas show typical subduction-type element distributions, with high ratios of fluid-mobile incompatible elements over fluid-immobile HFSE, Ba/Nb, for example, ranging between ca. 200 and 450. The lack of covariance between (e.g.) Ba/Nb and Ba/Th with 87Sr/ 86Sr, and Nd/Pb with Pb isotopic ratios suggests minimal involvement of sediment-derived metasomatism of the magmatic source. Geochemical character of the latter probably reflects contamination by hydrous fluids derived from altered oceanic crust (AOC). This is indicated by the coupling of relatively depleted, MORB-like Sr and Pb isotopic compositions and high Sr and Pb contents. Thus, given their N-MORB-type isotopic compositions, the LILE, and HFSE-like character, evidenced by high ratios of Ba/Nb, and variable Nd/Pb and Th/Nd, suggests NE Hokkaido arc magma genesis is best explained in terms of a binary mixing model involving: a dominantly N-MORB-like (i.e. depleted) convecting mantle 'wedge', contaminated by hydrous AOC

  5. Rapid Cenozoic ingrowth of isotopic signatures simulating "HIMU" in ancient lithospheric mantle: Distinguishing source from process

    NASA Astrophysics Data System (ADS)

    McCoy-West, Alex J.; Bennett, Vickie C.; Amelin, Yuri

    2016-08-01

    Chemical and isotopic heterogeneities in the lithospheric mantle are increasingly being recognised on all scales of examination, although the mechanisms responsible for generating this variability are still poorly understood. To investigate the relative behaviour of different isotopic systems in off-cratonic mantle, and specifically the origin of the regional southwest Pacific "HIMU" (high time integrated 238U/204Pb) Pb isotopic signature, we present the first U-Th-Pb, Rb-Sr, Sm-Nd and Re-Os isotopic dataset for spinel peridotite xenoliths sampling the subcontinental lithospheric mantle (SCLM) beneath Zealandia. Strongly metasomatised xenoliths converge to a restricted range of Sr and Nd isotopic compositions (87Sr/86Sr = 0.7028-0.7033; εNd ≈ +3-+6) reflecting pervasive overprinting of their original melt depletion signatures by carbonatite-rich melts. In contrast, rare, weakly metasomatised samples possess radiogenic Nd isotopic compositions (εNd > +15) and unradiogenic Sr isotopic compositions (87Sr/86Sr < 0.7022). This is consistent with melt extraction at ca. 2.0 Ga and in accord with widespread Paleoproterozoic Re-Os model ages from both weakly metasomatised and the more numerous, strongly metasomatised xenoliths. The coupling of chalcophile (Os), and lithophile (Sr and Nd) melt depletion ages from peridotite xenoliths on a regional scale under Zealandia argues for preservation of a significant mantle keel (⩾2 million km3) associated with a large-scale Paleoproterozoic melting event. Lead isotopic compositions are highly variable with 206Pb/204Pb = 17.3-21.3 (n = 34) and two further samples with more extreme compositions of 22.4 and 25.4, but are not correlated with other isotopic data or U/Pb and Th/Pb ratios in either strongly or weakly metasomatised xenoliths; this signature is thus a recent addition to the lithospheric mantle. Lead model ages suggest that this metasomatism occurred in the last 200 m.y., with errorchrons from individual localities

  6. Geochemistry of 24 Ma Basalts from Northeast Egypt: Implications for Small-Scale Convection Beneath the East African Rift System

    NASA Astrophysics Data System (ADS)

    Endress, C. A.; Furman, T.; Ali Abu El-Rus, M.

    2009-12-01

    Basalts ~24 Ma in the Cairo-Suez and Fayyum districts of NE Egypt represent the youngest and northernmost lavas potentially associated with the initiation of rifting of the Red Sea. The age of these basalts corresponds to a time period of significant regional magmatism that occurred subsequent to emplacement of 30 Ma flood basalts attributed to the Afar Plume in Ethiopia and Yemen. Beginning ~28 Ma, widespread magmatism occurred across supra-equatorial Africa in Hoggar (Algeria), Tibesti (Chad), Darfur (Sudan), Turkana (Kenya) and Samalat, Bahariya, Quesir and the Sinai Peninsula (Egypt) (e.g. Allegre et al., 1981; Meneisy, 1990; Baldridge et al., 1991; Wilson and Guiraud, 1992; Furman et al., 2006; Lucassen et al., 2008). Available geochemical and isotopic data indicate that Hoggar and Darfur basalts are similar to Turkana lavas, although no direct link between the N African lavas and the Kenya Plume has been made. New geochemical data on the NE Egyptian basalts provide insight into the thermochemical, isotopic, and mineralogical characteristics of the mantle beneath the region in which they were emplaced. The basalts are subalkaline with OIB-like incompatible trace element abundances and homogeneous major element, trace element and isotopic geochemistry. They display relatively flat ITE patterns, with notable positive Pb and negative P anomalies. Isotopic (143Nd/144Nd = 0.51274-0.51285, 87Sr/86Sr = 0.7049-0.7050) and trace element signatures (Ce/Pb = 16-22, Ba/Nb = 9-14, and La/Nb = 0.9-1.0) are consistent with melting of a sub-lithospheric source that has been slightly contaminated by continental crust during ascent and emplacement. The Pb isotopic ratios (206Pb/204Pb = 18.53-18.62, 207Pb/204Pb = 15.59-15.64, and 208Pb/204Pb = 38.80-39.00) in the Egyptian basalts are close to the range of those found in the 30 Ma Ethiopian flood basalts, which are distinct from the more highly radiogenic, high-μ type signature seen in basalts from Turkana, Darfur, and Hoggar

  7. Origin of the Red Dog Zn-Pb-Ag deposits, Brooks Range, Alaska: Evidence from regional Pb and Sr isotope sources

    USGS Publications Warehouse

    Ayuso, R.A.; Kelley, K.D.; Leach, D.L.; Young, L.E.; Slack, J.F.; Wandless, G.; Lyon, A.M.; Dillingham, J.L.

    2004-01-01

    Pb and Sr isotope data were obtained on the shale-hosted Zn-Pb-Ag Red Dog deposits (Qanaiyaq, Main, Aqqaluk, and Paalaaq), other shale-hosted deposits near Red Dog, and Zn-Pb-Ag sulfide and barite deposits in the western and central Brooks Range. The Red Dog deposits and other shale-hosted Zn-Pb-Ag deposits near Red Dog are hosted in the Mississippian Kuna Formation, which is underlain by a sequence of marine-deltaic clastic rocks of the Upper Devonian to Lower Mississippian Endicott Group. Ag-Pb-Zn vein-breccias are found in the Endicott Group. Galena formed during the main mineralization stages in the Red Dog deposits and from the Anarraaq and Wulik deposits have overlapping Pb isotope compositions in the range 206Pb/204Pb = 18.364 to 18.428, 207Pb/204Pb = 15.553 to 15.621, and 208Pb/204Pb = 38.083 to 38.323. Galena and sphalerite formed during the main ore-forming stages in the Red Dog deposits define a narrow field on standard uranogenic and thorogenic Pb isotope diagrams. Lead in sulfides of the Red Dog district is less radiogenic (238U/204Pb: ?? = 9.51-9.77) than is indicated by the average crustal lead evolution model (?? = 9.74), a difference consistent with a long history of evolution at low ratios of ?? before the Carboniferous. The homogeneous regional isotopic reservoir of Pb may indicate large-scale transport and leaching of minerals with various ?? ratios and Th/Pb ratios. Younger and genetically unrelated fluids did not significantly disturb the isotopic compositions of galena and sphalerite after the main mineralization event in the Red Dog district. Some pyrite shows evidence of minor Pb remobilization. The overall lead isotope homogeneity in the shale-hosted massive sulfide deposits is consistent with three types of control: a homogeneous regional source, mixing of lead during leaching of a thick sedimentary section and fluid transport, or mixing at the site of deposition. Isotopic variability of the hydrothermal fluids, as represented by galena

  8. Pb and O isotopic constraints on the source of granitic rocks from Cape Breton Island, Nova Scotia, Canada

    USGS Publications Warehouse

    Ayuso, R.A.; Barr, S.M.; Longstaffe, F.J.

    1996-01-01

    Pb isotopic compositions of leached feldspars from twenty-three plutons in Cape Breton Island can be divided into two groups: anorthosite, syenite, and granite in the Blair River Complex, which have the least radiogenic compositions on the Island, and granitic rocks from terranes (Aspy, Bras d'Or, and Mira) to the south. Pb isotopic data for the Blair River Complex (206Pb/204Pb = 17.399-18.107; 207Pb/204Pb = 15.505-15.560; 208Pb/204Pb = 36.689-37.733) are consistent with an old source region ultimately derived from the mantle and contaminated by sialic crust. Oxygen isotopic compositions of syenite in the Blair River Complex (??18O = +8.0 to +8.5 permil) are slightly higher than anorthosite (+7.0 to +8.3 permil); a Silurian granite in the Blair River Complex has ??18O = +7.5 permil. Cambrian to Devonian plutons in the Aspy, Bras d'Or, and Mira terranes are more radiogenic (206Pb/204Pb = 18.192-18.981; 207Pb/204Pb = 15.574-15.712; 208Pb/ 204Pb =37.815-38.936) than the Blair River Complex and were generated from source regions having a predominant crustal Pb signature (high ??). The ??18O values of granites and granodiorites in the Aspy terrane (+7.5 to +9.2 permil; avg = +8.6 permil) and Bras d'Or (+3.7 to +11.3 permil; avg = +9.4 permil) are also consistent with involvement of sialic crust. Many Late Proterozoic granites from the Mira terrane have anomalously low ??18O values (+0.2 to +5.9 permil), perhaps produced from protoliths that had undergone hydrothermal alteration prior to melting. Paleozoic granitic rocks from the Aspy, Bras d'Or, and Mira terranes cannot be uniquely distinguished on the basis of their Pb and O isotopic compositions. The granitic rocks could have been generated during terrane amalgamation from combinations of unradiogenic (Grenville-like) and more radiogenic (Avalon-like) sources.

  9. Geological, fluid inclusion and isotopic studies of the Yinshan Cu-Au-Pb-Zn-Ag deposit, South China: Implications for ore genesis and exploration

    NASA Astrophysics Data System (ADS)

    Wang, Guo-Guang; Ni, Pei; Wang, Ru-Cheng; Zhao, Kui-Dong; Chen, Hui; Ding, Jun-Ying; Zhao, Chao; Cai, Yi-Tao

    2013-09-01

    The Yinshan Cu-Au-Pb-Zn-Ag deposit is located in Dexing, South China. Ore bodies are primarily hosted in low-grade phyllite of the Neoproterozoic Shuangqiaoshan Group along EW- and NNW-striking fault zones. Pb-Zn-Ag mineralization is dictated by Jurassic rhyolitic quartz porphyries (ca. 172 Ma), whereas Cu-Au mineralization is associated with Jurassic dacite porphyries (ca. 170 Ma). The main ore minerals are pyrite, chalcopyrite, galena, sphalerite, tetrahedrite-tennatite, gold, silver, and silver sulphosalt, and the principal gangue minerals are quartz, sericite, calcite, and chlorite. Two-phase liquid-rich (type I), two-phase vapor-rich (type II), and halite-bearing (type III) fluid inclusions can be observed in the hydrothermal quartz-sulfides veins. Type I inclusions are widespread and have homogenization temperatures of 187-303 °C and salinities of 4.2-9.5 wt.% NaCl equivalent in the Pb-Zn-Ag mineralization, and homogenization temperatures of 196-362 °C and salinities of 3.5-9.9 wt.% NaCl equivalent in the Cu-Au mineralization. The pervasive occurrence of type I fluid inclusions with low-moderate temperatures and salinities implies that the mineralizing fluids formed in epithermal environments. The type II and coexisting type III inclusions, from deeper levels below the Cu-Au ore bodies, share similar homogenization temperatures of 317-448 °C and contrasting salinities of 0.2-4.2 and 30.9-36.8 wt.% NaCl equivalent, respectively, which indicates that boiling processes occurred. The sulfur isotopic compositions of sulfides (δ34S = -1.7‰ to +3.2‰) suggest a homogeneous magmatic sulfur source. The lead isotopes of sulfides (206Pb/204Pb = 18.01-18.07; 207Pb/204Pb = 15.55-15.57; and 208Pb/204Pb = 38.03-38.12) are consistent with those of volcanic-subvolcanic rocks (206Pb/204Pb = 18.03-18.10; 207Pb/204Pb = 15.56-15.57; and 208Pb/204Pb = 38.02-38.21), indicating a magmatic origin for lead in the ore. The oxygen and hydrogen isotope compositions (δ18O = +7.8

  10. Isotopic and incompatible element constraints on the genesis of island arc volcanics from Cold Bay and Amak Island, Aleutians, and implications for mantle structure

    NASA Astrophysics Data System (ADS)

    Morris, J. D.; Hart, S. R.

    1983-11-01

    Cold Bay and Amak Island, two Quaternary volcanic centers in the eastern Aleutians, are orthogonal relative to the trench and separated by ~50 km. Sr, Nd and Pb isotopic compositions of the calc-alkaline andesite magmas show no sign of contamination from continental crust (average 87Sr /86Sr = 0.70323 , 143Nd /144Nd = 0.51301 , 206Pb /204Pb = 18.82 , 207Pb /204Pb = 15.571 ). These samples plot within the mantle arrays for Sr-Nd and for Pb and are similar to arcs such as the Marianas and New Britain (Sr-Nd) and Marianas and Tonga (Pb). Incompatible element ratios for the Aleutian andesites (K/Rb ~ 332, K/Cs ~ 10,600, K/Sr ~ 22.4, K/Ba ~ 18.3, Ba/La ~ 60) are within the range reported for arc basalts, despite the difference in degree of fractionation. Average K content, K/Rb, K/Ba and K/Sr are approximately the same for basalts from arcs and from oceanic islands (OIB); K/Cs is a factor of 4 lower and Ba/La almost 3 times higher in arcs. Abundance ratio correlations indicate that arcs are enriched in Cs and depleted in La relative to OIB, with other incompatible element abundances very similar. Histograms of Sr and Nd isotopic compositions for MORB, OIB, and intraoceanic arcs show remarkably similar peaks and distribution patterns for intraoceanic arcs and OIB. A "plum pudding" model for the upper mantle best accommodates a) geochemical coherence of OIB and IAV, b) the existence of mantle plumes at some oceanic islands, and c) the presence of a MORB-type source at back arc spreading centers. In this model, OIB plums are imbedded in a MORB matrix; small degrees of melting generate OIB-type magmas while larger degrees of melting dilute the OIB magma with MORB matrix melts. OIB plums are merely less robust lower mantle plumes ( i.e., blobs) which are distributed throughout the upper mantle by convection. The existence of at least two types of OIB, as indicated by Sr, Nd, and Pb isotopes, suggests that nuggets of recycled oceanic lithosphère may coexist with lower

  11. Petrogenesis of synorogenic diorite-granodiorite-granite complexes in the Damara Belt, Namibia: Constraints from U-Pb zircon ages and Sr-Nd-Pb isotopes

    NASA Astrophysics Data System (ADS)

    Jung, S.; Kröner, A.; Hauff, F.; Masberg, P.

    2015-01-01

    The synorogenic Palmental complex (central Damara Belt, Nambia) consists of ca. 545 Ma old quartz diorites and rare granodiorites and ca. 520 Ma-old leucogranites, representing one of the earliest and most primitive phase of crustal plutonism predating the main high-T regional metamorphism. Most quartz diorites and one granodiorite evolved through multistage, polybaric evolutionary processes involving fractionation from a lithospheric mantle-derived melt, followed by fractional crystallization of mainly hornblende, plagioclase and apatite which is shown by decreasing MgO, FeO, CaO, TiO2 and P2O5 with increasing SiO2. Assimilation of felsic basement gneisses was also important during formation of these granitoids. Although their chemical characteristics (high LILE, low HFSE) resemble those of quartz diorites and granodiorites with calc-alkaline affinity, they differ in their enriched Sr (initial 87Sr/86Sr: 0.7061-0.7098) and Nd (initial εNd: -2.7 to -9.9) isotopic composition. Neodymium depleted mantle mean crustal residence ages range from 1.3 to 1.9 Ga for the quartz diorites including the granodiorite. These model ages correlate with major and trace element abundances, further substantiating that AFC processes modified the initial isotopic systematics. Lead (206Pb/204Pb: 17.43-17.68, 207Pb/204Pb: 15.61-15.66, 208Pb/204Pb: 38.19-38.49) isotopic composition are unradiogenic relative to other Damaran intrusive rocks but plot above the Stacey and Kramers (1975) reference line, indicating that the source underwent an ancient (pre Pan-African) increase in U/Pb and Th/U, followed by more recent U-depletion. Some variation in 206Pb/204Pb at high 207Pb/204Pb further indicates involvement of ancient crustal material, most likely through AFC processes. A cross-cutting leucogranite dyke has also evolved isotopic compositions (initial 87Sr/86Sr: 0.7326; initial εNd: -15.6; 206Pb/204Pb: 17.42, 207Pb/204Pb: 15.62, 208Pb/204Pb: 38.16) but in view of the apparent younger age of

  12. Geological, rare earth elemental and isotopic constraints on the origin of the Banbanqiao Zn-Pb deposit, southwest China

    NASA Astrophysics Data System (ADS)

    Li, Bo; Zhou, Jia-Xi; Huang, Zhi-Long; Yan, Zai-Fei; Bao, Guang-Ping; Sun, Hai-Rui

    2015-11-01

    The newly discovered Banbanqiao Zn-Pb deposit in the southeastern part of the Sichuan-Yunnan-Guizhou (SYG) Pb-Zn metallogenic province is located on the western Yangtze Block, southwest China. Ore bodies of the Banbanqiao deposit are stratiform type, host in dolomitic limestone and dolostone of the Lower Carboniferous Dapu Formation and occur within the NNE-trending Banbanqiao anticline. More than 1.5 million tones (Mt) Zn-Pb ores at grades of 0.26-10.32 wt.% Pb and 0.81-28.8 wt.% Zn have been controlled until now. δ13CPDB and δ18OSMOW values of calcite separates range from -2.8‰ to -0.7‰ (average -1.1‰) and +14.1‰ to +17.0‰ (average +15.5‰), respectively. The δ13CPDB values are similar to those of marine carbonate rocks, but higher than those of mantle and significantly different from those of sedimentary organic matter. However, the δ18OSMOW values are among those of mantle, marine carbonate rocks and sedimentary organic matter. δ34SCDT values of sulfide separates range from +3.2‰ to +9.9‰ (average +6.5‰), unlike mantle-derived sulfur (0 ± 3‰), whilst lower than evaporites (+22‰ to +28‰) within host strata. 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values of country shale and dolostone whole-rock samples are 18.47, 15.66 and 38.70, and 18.44-18.60, 15.66-15.85 and 38.70-39.14, respectively. Sulfide separates have 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values ranging from 18.03 to 18.73, 15.65 to 15.78 and 38.15 to 39.14, respectively. These Pb isotopic data indicate a clearly crustal source of Pb in the plot of 207Pb/204Pb vs. 206Pb/204Pb. Total REE (ΣREE) contents of country shale and dolostone whole-rock samples are 2.63 ppm and 0.72-86.2 ppm with δEu values are 2.79 and 0.34-0.70, respectively. Pyrite, sphalerite, galena and calcite samples have ΣREE contents of 5.3-36.4 ppm, 0.29-3.39 ppm, 0.52 ppm and 22.0-41.1 ppm, respectively, and δEu values of 0.64-0.86, 0.94-2.86, 0.32 and 0.21-0.45, respectively. These rare earth

  13. A petrologic study of the Teanaway Basalt: Eocene slab window volcanism in central WA

    NASA Astrophysics Data System (ADS)

    Roepke, E.; Tepper, J. H.; Ivener, D.

    2013-12-01

    The Teanaway Basalt (TB) includes subaerial basalt to andesite flows, mafic to felsic tuffs, and rhyolite domes in the Central Cascades of Washington State. These volcanics overlie the extensive ~47 Ma Teanaway Dike Swarm (TDS) that cuts the underlying Swauk Formation. This study focuses on the tectonic setting of eruption and geochemical variations relating to geography and stratigraphy within the TB. The western-most area of the TB, Easton Ridge (ER), is compared with the eastern-most area of the TB, Liberty Ridge (LR) - 40 km to the east of ER. The bimodal TB consists predominantly of basaltic andesite and andesite (45.3-63.1 wt% SiO2) with subordinate rhyolite (75.9-79.4 wt% SiO2). The mafic rocks classify as primarily medium-K tholeiites (0.1-3.0 wt% K2O), but a few samples classify as alkaline. Enrichment in LILE and depletion in HFSE on spidergrams are indicative of an arc setting. However, compared with the modern Cascade Arc, the TB is distinctly higher in Fe2O3T (8.8-17.1 wt%) and TiO2 (1.1-2.7 wt%), and distinctly lower in Al2O3 (11.2-14.6) and K2O, with a similar range of Mg #s (0.15-0.48). Most tectonic discrimination plots characterize the TB as MORB, but some indicate an arc or within-plate setting. Preliminary Pb isotopic data (206Pb/204Pb = 19.13-19.19, 207Pb/204Pb = 15.62-15.64, and 208Pb/204Pb = 38.78-38.90) indicate the TB and TDS are more enriched than Cascade Arc rocks in 206Pb/204Pb and 208Pb/204Pb. Overall, these geochemical data are consistent with a model in which asthenospheric mantle ascending through a slab window interacts with mantle wedge that has previously acquired arc chemical traits. The existence of a slab window in this region during the mid-Eocene is compatible with plate reconstructions and evidence of extension that have been attributed to subduction of the Resurrection-Kula ridge (Haeussler et al., 2003). Harker plots show lavas at LR are generally more enriched than those at ER in Fe2O3T (11.9-17.1 wt% vs 8.8-15.7 wt%) Mn

  14. 40Ar/39Ar geochronology and geochemical reconnaissance of the Eocene Lowland Creek volcanic field, west-central Montana

    USGS Publications Warehouse

    Dudas, F.O.; Ispolatov, V.O.; Harlan, S.S.; Snee, L.W.

    2010-01-01

    We report geochronological and geochemical data for the calc-alkalic Lowland Creek volcanic field (LCVF) in westcentral Montana. 40Ar/ 39Ar age determinations show that the LCVF was active from 52.9 to 48.6 Ma, with tuff-forming eruptions at 52.9 ?? 0.14 and 51.8 ?? 0.14 Ma. These dates span the age range of vigorous Eocene igneous activity in the Kamloops-Absaroka-Challis belt. The LCVF evolved upward from basal rhyolites (SiO 2>71 wt%) to dacites and andesites (SiO 2 > 62 wt%). Compositional change parallels a transition from early explosive volcanism to late effusive activity. Four geochemical components can be detected in the rocks. A component with 206Pb/204Pb < 16.5 and epsilon;Nd near-15 is predominant in anhydrous, two-pyroxene dacites; hydrous rhyolites, rhyodacites, and dacites with epsilon;Nd below-10 are dominated by a second component; hydrous rocks with 206Pb/ 204Pb > 18.3 and epsilon;Nd>-9 contain a third component; and an andesite with low Nd content and epsilon;Nd near-9 probably contains a fourth component. The first three components probably derive from the lower and middle crust, whereas the fourth is probably from the lithospheric mantle. ?? 2010 by The University of Chicago.

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

    NASA Astrophysics Data System (ADS)

    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

  16. Barremian rift-related turbidites and alkaline volcanism in southern Mexico and their role in the opening of the Gulf of Mexico

    NASA Astrophysics Data System (ADS)

    Mendoza-Rosales, Claudia C.; Centeno-García, Elena; Silva-Romo, Gilberto; Campos-Madrigal, Emiliano; Bernal, Juan Pablo

    2010-07-01

    The Chivillas Formation is the easternmost record of Mesozoic marine volcanism in Mexico. It consists of thick intervals of pillow lavas interbedded with siliciclastic turbidites, and debrites, containing clasts derived from metamorphic, sedimentary and volcanic sources. Clast composition and detrital zircon geochronology indicate a continental provenance, with sources located south of the studied rocks. Detrital zircon ages range from 1573 ± 60 to 125 ± 1.6 Ma. The probability curves have peaks at 124 to 130 Ma (mean 126 Ma); 188 Ma and 921-1236 Ma (the latter with peaks at ˜ 1022 and ˜ 1157 Ma). Subordinate peaks at 277, 419 and 535 Ma are also present. We interpret the youngest zircon population ˜ 126 Ma (Barremian), as the maximum depositional age. Other peaks suggest Grenvillian-type basement and Permo-Triassic arc sources. Late Jurassic detrital zircons were probably derived from the Sierra de Juárez Mylonitic belt. Pillow lavas are mostly alkaline basalts, with SiO 2 46%-53%, and alkali oxide (K 2O + Na 2O) 5-8 wt.%; all samples have low-TiO 2 (< 1.6 wt.%) and low V (180-242 ppm), with Ti/V between 30 and 50. 206Pb/ 204Pb isotopic ratios are 18.6-20.5, and 208Pb/ 204Pb are 38.4-40.3, within OIB and MORB ranges. Initial ɛNd(126) are 0.3 to 4.1, and TDM are 632-1520 Ma. Lava compositions are similar to alkaline basalts along the margins of the Atlantic Ocean, particularly to basalts from the Central Atlantic Magmatic Province (CAMP), and to the Cretaceous Peri-Atlantic Alkaline Pulse (PAAP). Volcano-sedimentary rocks from Chivillas Formation probably formed in a subsiding marine rift basin, at a ridge-transform intersection. This basin received sediments transported throughout longitudinal canyons along the major Jurassic-Cretaceous strike-slip fault. In this model, extension of the rift basin was controlled by right-lateral displacement of the strike-slip fault, which acted as a transform fault at this time. This rift is interpreted as a segment of the

  17. Sr, Nd and Pb isotopes in Proterozoic intrusives astride the Grenville Front in Labrador: Implications for crustal contamination and basement mapping

    USGS Publications Warehouse

    Ashwal, L.D.; Wooden, J.L.; Emslie, R.F.

    1986-01-01

    We report Sr, Nd and Pb isotopic compositions of mid-Proterozoic anorthosites and related rocks (1.45-1.65 Ga) and of younger olivine diabase dikes (1.4 Ga) from two complexes on either side of the Grenville Front in Labrador. Anorthositic or diabasic samples from the Mealy Mountains (Grenville Province) and Harp Lake (Nain-Churchill Provinces) complexes have very similar major, minor and trace element compositions, but distinctly different isotopic signatures. All Mealy Mountains samples have ISr = 0.7025-0.7033, ??{lunate}Nd = +0.6 to +5.6 and Pb isotopic compositions consistent with derivation from a mantle source depleted with respect to Nd/Sm and Rb/Sr. Pb isotopic compositions for the Mealy Mountains samples are slightly more radiogenic than model mantle compositions. All Harp Lake samples have ISr = 0.7032-0.7066, ??{lunate}Nd = -0.3 to -4.4 and variable, but generally unradiogenic 207Pb 204Pb and 206Pb 204Pb compared to model mantle, suggesting mixing between a mantle-derived component and a U-depleted crustal contaminant. Crustal contaminants are probably a variety of Archean high-grade quartzofeldspathic gneisses with low U/Pb ratios and include a component that must be isotopically similar to the early Archean (>3.6 Ga) Uivak gneisses of Labrador or the Amitsoq gneisses of west Greenland. This would imply that the ancient gneiss complex of coastal Labrador and Greenland is larger than indicated by present surface exposure and may extend in the subsurface as far west as the Labrador Trough. If Harp Lake and Mealy Mountains samples were subjected to the same degree of contamination, as suggested by their chemical similarities, then the Mealy contaminants must be much younger, probably early or middle Proterozoic in age. The Labrador segment of the Grenville Front, therefore, appears to coincide with the southern margin of the Archean North Atlantic craton and may represent a pre mid-Proterozoic suture. ?? 1986.

  18. Taming the Mighty Mississippi: Integrating paleo-flood data and modeling to understand the patterns and causes of extreme floods on a major river system

    NASA Astrophysics Data System (ADS)

    Munoz, Samuel; Giosan, Liviu; Jeffrey, Donnelly; Dee, Sylvia; Shen, Zhixiong

    2016-04-01

    The Mississippi River is an economic artery of the United States that is heavily managed to provide flood control and maintain a navigable shipping channel. The current system of levees and spillway structures was conceived in the early 20th century, but the ability of this system to withstand the altered hydroclimatic conditions projected for the next century is poorly understood. Here, we present initial results from a project that integrates new sedimentary records from floodplain lakes with analyses of sediment geochemistry and climate model simulations to better understand the causes of extreme floods on the lower Mississippi River. In our sedimentary paleoflood records, flood event beds are characterized by an upward fining sequence from deposition of the bedload and suspended load during overbank floods, identified here using high-resolution laser particle-size analysis and elemental composition (XRF), and dated using radioisotopes (137Cs, 210Pb, 14C) and optically-stimulated luminescence (OSL) on quartz. Grain-size descriptors and elemental ratios of Zr/Fe and Fe/Rb are highly correlated, and are used alongside historical discharge records to develop a statistical model for reconstructing flood magnitude in prehistoric contexts. Geochemical analyses of sediments from the floodplains of major tributaries of the Mississippi are used to assess the systematics of 87Sr/86Sr, 143Nd/144Nd, 206Pb/204Pb, and 208Pb/204Pb across the basin, enabling identification of the synoptic patterns of individual paleo-flood events. We investigate the dynamical drivers of past floods on the lower Mississippi using both reanalysis data and the last millennium simulation from NCAR model CESM1 to find that increased likelihoods of extreme floods on the lower Mississippi River are associated with enhanced moisture flux over midcontinental North America that is controlled by the interaction of seasonally variable soil moisture over major tributaries with inter-annual (e.g., ENSO) and

  19. Pb isotopic variability in the modern-Pleistocene Indus River system measured by ion microprobe in detrital K-feldspar grains

    NASA Astrophysics Data System (ADS)

    Alizai, Anwar; Clift, Peter D.; Giosan, Liviu; VanLaningham, Sam; Hinton, Richard; Tabrez, Ali R.; Danish, Muhammad; Edinburgh Ion Microprobe Facility (EIMF)

    2011-09-01

    The western Himalaya, Karakoram and Tibet are known to be heterogeneous with regard to Pb isotope compositions in K-feldspars, which allows this system to be used as a sediment provenance tool. We used secondary ion mass spectrometry to measure the isotopic character of silt and sand-sized grains from the modern Sutlej and Chenab Rivers, together with Thar Desert sands, in order to constrain their origin. The rivers show a clear Himalayan provenance, contrasting with grains from the Indus Suture Zone, but with overlap to known Karakoram compositions. The desert dunes commonly show 207Pb/ 204Pb and 206Pb/ 204Pb values that are much higher than those seen in the rivers, most consistent with erosion from Nanga Parbat. This implies at least some origin from the trunk Indus, probably reworked by summer monsoon winds from the SW, a hypothesis supported by bulk Nd and U-Pb zircon dating. Further data collected from Holocene and Pleistocene sands shows that filled and abandoned channels on the western edge of the Thar Desert were sourced from Himalayan rivers before and at 6-8 ka, but that after that time the proportion of high isotopic ratio grains rose, indicating increased contribution from the Thar Desert dunes prior to ˜4.5 ka when flow ceased entirely. This may be linked to climatic drying, northward expansion of the Thar Desert, or changes in drainage style including regional capture, channel abandonment, or active local Thar tributaries. Our data further show a Himalayan river channel east of the present Indus, close to the delta, in the Nara River valley during the middle Holocene. While this cannot be distinguished from the Indus it is not heavily contaminated by reworking from the desert. The Pb system shows some use as a provenance tool, but is not effective at demonstrating whether these Nara sediments represent a Ghaggar-Hakra stream independent from the Indus. Our study highlights an important role for eolian reworking of floodplain sediments in arid rivers

  20. Syn-orogenic high-temperature crustal melting: Geochronological and Nd-Sr-Pb isotope constraints from basement-derived granites (Central Damara Orogen, Namibia)

    NASA Astrophysics Data System (ADS)

    Ostendorf, Jörg; Jung, Stefan; Berndt-Gerdes, Jasper; Hauff, Folkmar

    2014-04-01

    Major and trace element and Nd, Sr and Pb isotope data from c. 550 Ma-old gray granites and c. 510 Ma-old red leucogranites of the high-grade central part of the Damara orogen (Namibia) indicate a dominantly deep crustal origin. Moderately peraluminous gray granites are isotopically evolved (initial ɛNd: c. - 17) and were likely derived from meta-igneous sources with late Archean to Paleoproterozoic crustal residence ages. Based on a comparison with experimental results, the granites were derived by partial melting of a granodioritic biotite gneiss at c. 900-950 °C and less than 10 kbar. Slightly peraluminous red leucogranites are also isotopically evolved (initial ɛNd: - 15 to - 18) but have undergone extensive crystal fractionation coupled with minor contamination of mid crustal meta-pelitic material. Major and trace element data do not support closed-system fractional crystallization processes for all samples, however, some chemical features underline the importance of crystal fractionation processes especially for the leucogranites. Isotope data do not support mixing of different crust-derived melts or assimilation of crustal rocks by a mafic magma on a large scale. For the gray granites, unradiogenic Pb isotope compositions with substantial variation in 207Pb/204Pb at almost constant 206Pb/204Pb, strongly negative ɛNd values and moderately radiogenic Sr isotope compositions argue for an undepleted nature of the source. High Rb/Sr ratios of the red leucogranites permit a comparison with the gray granites but similar initial ɛNd values indicate that the source of these granites is not fundamentally different to the source of the gray granites. The most acceptable model for both granite types involves partial melting of meta-igneous basement rocks of Archean to Proterozoic age. The consistency of the chemical data with a crustal anatectic origin and the observation that the gray granites intruded before the first peak of high-grade regional metamorphism

  1. Genesis of ilmenite-series I-type granitoids at the Baogutu reduced porphyry Cu deposit, western Junggar, NW-China

    NASA Astrophysics Data System (ADS)

    Cao, MingJian; Qin, KeZhang; Li, GuangMing; Evans, Noreen J.; Hollings, Pete; Jin, LuYing

    2016-03-01

    The Baogutu porphyry Cu deposit is a typical reduced porphyry Cu deposit, likely related to ilmenite-series I-type granitoids. However, the nature of the granitoids (ilmenite-series or magnetite-series) and the genesis of the Baogutu deposit are still under debate. In order to resolve these issues, whole-rock magnetic susceptibility, geochemistry and Sr-Nd-Pb isotopic, zircon U-Pb dating and Hf-O isotopic compositions were carried out. Three different intrusive phases are recognized within the deposit, from oldest to youngest, they are diorite with trace gabbro, diorite-granodiorite porphyry, and hornblende diorite porphyry, all of which were emplaced in the Late Carboniferous (320-306 Ma) and show a metaluminous, calc-alkaline I-type granitoid character with typical supra-subduction zone geochemical affinities. The intrusions are characterized by widespread primary pyrrhotite without anhydrite and hematite, dominant ilmenite over magnetite, low whole rock magnetic susceptibility (< 1 × 10- 4 emu g- 1 oe- 1 or < 3 × 10- 3 SI unit) and low whole rock Fe2O3/FeO ratios (< 0.4), indicating that the granitoids are ilmenite- rather than magnetite-series I-type granitoids. Whole rock Sr-Nd-Pb isotopic compositions show limited variation but slightly enriched characteristics with (87Sr/86Sr)i values of 0.70357-0.70404, εNd (t) of + 6.3 to + 7.8, 206Pb/204Pb of 18.20-19.54 and 208Pb/204Pb of 37.97-39.55. Zircon Hf-O isotopic compositions show εHf (t) values of + 10.7 to + 15.8 and δ18O of 5.3-7.4‰. Zircon and apatite saturation thermometries yield temperatures of 720 to 920 °C with relatively higher temperatures for the porphyries than for the diorite. Limited variations in Sr-Nd-Pb-Hf-O isotopic compositions and extremely young whole rock T2DM (Nd) (430 to 570 Ma) and zircon TDMC (Hf) (310 to 640 Ma) do not indicate significant crustal contamination during magma ascent or emplacement. Rather the Baogutu ilmenite-series I-type granitoids were probably formed by

  2. Lead isotope and Pb-Pb model age determinations of ores from Central Europe and their metallogenetic interpretation

    NASA Astrophysics Data System (ADS)

    Bielicki, K.-H.; Tischendorf, G.

    1991-02-01

    The paper presents lead isotope data from 211 samples from Phanerozoic lead-bearing ore occurrences in Central Europe, particularly from the Southern part of the former German Democratic Republic. The data are interpreted in terms of Amov's dynamic model of continuous lead isotope evolution. The relationships between thoro-genic and urano-genic model ages and the source of lead in different regional units are discussed. We observed differences in lead isotope evolution in the Hercynian internides and externides. Within the Moldanubian and Saxothuringian zones we distinguish five main lead-bearing ore associations: (1) Cambrian, stratiform base metal (Hermsdorf-Waldsassen; 206Pb/ 204Pb=17.50 17.70), (2) Devonian, vein type Sb-bearing, metamorphogene (neumühle-Hartmannsdorf; 17.80 18.00), (3) Upper Carboniferous-Permian, polymetallic, including tin, vein type (Kutna hora-Freiberg-Altenberg; 18.00 18.20), (4) Triassic (-Jurassic), Pb-Ba, vein type (Střibro-Halsbrücke; 18.20 18.60), (5) Cenozoic, polymetallic, vein type, riftogene (Roztoky-Banska Štiavnica; 18.80 19.10). Pb isotope characteristics from ores of the Montagne Noire and the Brioude-Massiac district correspond to this subdivision. Ore associations from the Rheno-Hercynian zone display higher 207Pb/204Pb ratios which can be explained by more evolved and less metamorphosed source rocks. Mineralizations of the eastern Harz (Straßberg-Neudorf) belong to the Permian association, those from the western Harz (Clausthal-Bad Grund) to the Triassic-Jurassic. Because of Pb isotope agreement the stratabound Rammelsberg and the vein bound Ramsbeck-I mineralization are presumed to be isogenetic. Pb isotope identity of distinct mineralizations in the basement zone (Halsbrücke-Bad Grund) and in the Triassic sediments (Gorny Slask-Mechernich-Bleiglanzbänke) suggests a strong genetic coherence. Pb isotope conformity between the Upper Carboniferous-Permian-Triassic ore associations and Hercynian postkinematic

  3. CHRONOLOGICAL CONSTRAINTS ON FLUID CIRCULATION IN MESOZOIC FORMATIONS OF THE EASTERN PART OF THE PARIS BASIN INFERRED FROM U-Pb DATING OF SECONDARY INFILLING CARBONATES

    NASA Astrophysics Data System (ADS)

    Pisapia, C.; Deschamps, P.; Hamelin, B.; Buschaert, S.

    2009-12-01

    equilibrium composition, indicating that the precipitation phase was older than 650 ky. U-Pb measurements were performed on a VG sector Thermal Ionization Mass Spectrometer (TIMS) using a 205Pb-236U-233U-229Th spike. Pb contents are generally very low, between 3 and 20 ppb, while U contents are more variable, leading to μ = 238U/204Pb up to ~600. Sub-samples with high μ show radiogenic 206Pb/204Pb ratio, but at this stage isochrons generally show high scatter. These U-Pb data however are consistent with an Eocene-Oligocene period for the late carbonates precipitation phase. We will discuss the different processes that may be responsible for these errorchrons (i.e. heterogeneities in the initial isotopic composition; multi-stage growth) as well as the chronological constraints that can be drawn from these data.

  4. Pb-Sr-O-C isotope compositions of metacarbonate rocks of the Derbina Formation (East Sayan): Chemostratigraphic and geochronological significance

    NASA Astrophysics Data System (ADS)

    Gorokhov, I. M.; Kuznetsov, A. B.; Ovchinnikova, G. V.; Nozhkin, A. D.; Azimov, P. Ya.; Kaurova, O. K.

    2016-01-01

    The Pb-Sr-O-C isotope compositions of calcite marbles of the Derbina Formation, exposed in the northwestern part of the Derbina block of the East Sayan, were studied. Rocks of the Derbina Formation were metamorphosed under high-temperature amphibolite facies conditions. The carbonate constituent of marbles contains (ppm) 15-130 Mn, 130-160 Fe, 0.008-0.039 Rb, 645-2190 Sr, 0.565-0.894 U, and 0.288-1.42 Pb. These concentrations are similar to those in modern carbonate sediments. The values of δ13C in marbles of the Derbina Formation range from-0.6 to +1.4‰ PDB; the values of δ18O range from 21.5 to 28.6‰ SMOW. The 87Sr/86Sr ratio values in the two least altered rocks, which meet geochemical criteria of the Rb-Sr system preservation in high-grade carbonate rocks, are 0.70804 and 0.70829. The protolith ages of marbles determined using Sr and C chemostratigraphy lie within the interval of 560-530 Ma, which is regarded as the period of carbonate sedimentation. The slope of the straight line on the 206Pb/204Pb-207Pb/204Pb diagram ( n = 9, MSWD = 19) constructed on the basis of the data points of bulk carbonate constituents of all samples studied and those representing leachate steps of one of them in 0.5N HBr yields Late Vendian age (556 ± 31 (2σ) Ma. Taking into account the data on Sr and C isotope systematics of Derbina marbles, this age is regarded as the age of early diagenesis of carbonate sediments close to the age of sedimentation. Thus, metacarbonate rocks of the Derbina Formation preserved the pre-metamorphic chemostratigraphic and isotope-geochronological information. The age obtained testifies that formation of the carbonate cover of the Derbina block occurred in the Late Vendian. At the end of the Cambrian, carbonate deposits were metamorphosed during the Early Caledonian tectonic event in the southeastern part of the Central Asian Fold Belt.

  5. The early formation of the IVA iron meteorite parent body

    NASA Astrophysics Data System (ADS)

    Blichert-Toft, Janne; Moynier, Frédéric; Lee, Cin-Ty A.; Telouk, Philippe; Albarède, Francis

    2010-08-01

    The IVA iron meteorites are magmatic cumulates from the core of a small asteroid, which broke apart ˜ 400 Ma ago. As the depletion of this planetary body in volatile elements is expected to be reflected in high U/Pb ratios of its minerals, we embarked on analyzing the isotope composition of Pb in the cm-sized troilite inclusions of Muonionalusta and Gibeon, both iron meteorites belonging to the IVA family. The bulk of the data for nine troilite subsamples of Muonionalusta scatter with an apparent age of 4.57 Ga, which is shown to reflect the presence of both primordial and common terrestrial Pb components, in addition to radiogenic Pb. The most radiogenic subsample, however, has fractions with 206Pb/ 204Pb ratios as high as over 1000 and gives a statistically significant 207Pb*/ 206Pb* age of 4565.3 ± 0.1 Ma (MSWD = 0.08), consistent with the 182Hf- 182W metal-silicate segregation age of 2.4 ± 2.0 Ma. These data make the age of Muonionalusta the oldest documented yet for all differentiated bodies in the Solar System and constitute the first high-precision Pb-Pb age determined for crystallization of a phase contained within an iron meteorite group, hence advancing our understanding of early Solar System chronology. Using literature values for the cooling rate, and assuming a closure temperature for Pb of 300 °C, it is further estimated that the IVA parent body accreted within 1 Ma of CAI formation and had cooled to the Pb closure temperature within an additional 1-2 Ma. The overlap between the high-precision Pb-Pb and Hf-W ages points to a small, or rapidly fragmented, planetary body. The isotopic composition of Pb in Gibeon troilite yields a significantly younger age of 4544 ± 7 Ma (MSWD = 1.5), consistent with evidence from the 107Pd- 107Ag chronometer, but we believe this age has been reset by melting upon shock. One puzzling observation is that the apparent 232Th/ 238U of Muonionalusta troilite is particularly low (˜ 0.32), requiring a mechanism capable of

  6. Copahue volcano and its regional magmatic setting

    USGS Publications Warehouse

    Varekamp, J C; Zareski, J E; Camfield, L M; Todd, Erin

    2016-01-01

    Copahue volcano (Province of Neuquen, Argentina) has produced lavas and strombolian deposits over several 100,000s of years, building a rounded volcano with a 3 km elevation. The products are mainly basaltic andesites, with the 2000–2012 eruptive products the most mafic. The geochemistry of Copahue products is compared with those of the main Andes arc (Llaima, Callaqui, Tolhuaca), the older Caviahue volcano directly east of Copahue, and the back arc volcanics of the Loncopue graben. The Caviahue rocks resemble the main Andes arc suite, whereas the Copahue rocks are characterized by lower Fe and Ti contents and higher incompatible element concentrations. The rocks have negative Nb-Ta anomalies, modest enrichments in radiogenic Sr and Pb isotope ratios and slightly depleted Nd isotope ratios. The combined trace element and isotopic data indicate that Copahue magmas formed in a relatively dry mantle environment, with melting of a subducted sediment residue. The back arc basalts show a wide variation in isotopic composition, have similar water contents as the Copahue magmas and show evidence for a subducted sedimentary component in their source regions. The low 206Pb/204Pb of some backarc lava flows suggests the presence of a second endmember with an EM1 flavor in its source. The overall magma genesis is explained within the context of a subducted slab with sediment that gradually looses water, water-mobile elements, and then switches to sediment melt extracts deeper down in the subduction zone. With the change in element extraction mechanism with depth comes a depletion and fractionation of the subducted complex that is reflected in the isotope and trace element signatures of the products from the main arc to Copahue to the back arc basalts.

  7. Rare-earth elements and Nd and Pb isotopes as source indicators for Labrador Sea clay-size sediments during Heinrich event 2

    USGS Publications Warehouse

    Benson, L.; Barber, David; Andrews, John T.; Taylor, H.; Lamothe, P.

    2003-01-01

    Elemental abundances and Nd and Pb isotope ratios were determined on samples from the carbonate-free, clay-size fractions of sediments from intervals above, within, and below Heinrich event 2 (H-2) in core HU87-9 from the Northwest Labrador Sea slope. In HU87-9, rare-earth element (REE) distributions and elemental concentrations within the H-2 event are distinct from those outside this event, ??Nd(0) and 206Pb/204Pb data also indicate different values for sediments deposited within and outside the H-2 event. Comparisons of REE patterns from the H-2 interval with those from bedrock units in Baffin Island, northern Quebec, and Labrador indicate that the Lake Harbour Group (LHG), which crops out on the north side of the Hudson Strait, is the most probable bedrock source of the clay-size fraction found within the H-2 interval in HU87-9. The Tasiuyak Gneiss (TG) and Lac Lomier Complex (LLC) have REE patterns (including a negative Eu anomaly) similar to those found in H-2 sediments; however, the La/Yb ratios of these units are smaller than those associated with H-2 sediments. The Nd and Pb isotope data support and complement REE-based interpretations of provenance; i.e., the Nd-Pb signatures of sediments deposited at the HU87-9 site during the H-2 event are similar to Nd-Pb signatures obtained on diamicts from the western end of Hudson Strait. Published by Elsevier Science Ltd.

  8. Back-arc basalts from the Loncopue graben (Province of Neuquen, Argentina)

    NASA Astrophysics Data System (ADS)

    Varekamp, J. C.; Hesse, A.; Mandeville, C. W.

    2010-11-01

    Young basaltic back-arc volcanoes occur east of the main Andes chain at about 37.5°-39°S in the Loncopue graben, Province of Neuquen, Argentina. These olivine-rich basalts and trachybasalts have up to 8% MgO, with high Ni and Cr contents, but highly variable incompatible element concentrations. Mafic lava flows and cinder cones at the southern end of the graben lack phenocrystic plagioclase. The northern samples have relative Ta-Nb depletions and K, Pb and LREE enrichment. These samples strongly resemble rocks of the nearby arc volcanoes Copahue and Caviahue, including their Fe-Ti enrichment relative to the main Andes arc rocks. The Sr, Nd and Pb isotope ratios show that the source regions of these back-arc basalts are enriched in subducted components that were depleted in the aqueous mobile elements such as Cs, Sr and Ba as a result of prior extractions from the subducted complex below the main arc. Some mafic flows show slightly low 206Pb/ 204Pb and 143Nd/ 144Nd values as well as incompatible trace element ratios similar to southern Patagonia plateau back-arc basalts, suggesting contributions from an EM1 mantle source. Geothermometry and barometry suggest that the basalts crystallized and fractionated small amounts of olivine and spinel at ˜ 35 km depth at temperatures of 1170-1220 °C, at about QFM + 0.5 to QFM + 1 with 1-2% H 2O, and then rose rapidly to the surface. The Loncopue graben back-arc basalts are transitional in composition between the South Patagonia back-arc plateau basalts and the Caviahue and Copahue arc volcanoes to the northwest. The EM1 source endmember is possibly the subcontinental lithospheric mantle. Strong variations in incompatible element enrichment and isotopic compositions between closely spaced cinder cones and lava flows suggest a heterogeneous mantle source for the Loncopue graben volcanics.

  9. The sources and time-integrated evolution of diamond-forming fluids - Trace elements and isotopic evidence

    NASA Astrophysics Data System (ADS)

    Klein-BenDavid, Ofra; Pearson, D. Graham; Nowell, Geoff M.; Ottley, Chris; McNeill, John C. R.; Logvinova, Alla; Sobolev, Nikolay V.

    2014-01-01

    , kimberlite-like 206Pb/204Pb and 208Pb/204Pb ratios. A multi-stage evolution of the diamond-forming fluids source can be constrained from our new isotopic data, indicating an Achaean enrichment event resulting in elevated U/Pb, Rb/Sr ratios and enrichment in LREEs. This source underwent a more recent fractionation, in the last 500 Myr that may have been related to the diamond-forming event. There is a strong correspondence between fluids with relatively unradiogenic Sr isotopes and relatively low (La, Nd, Sm)/(Nb, Zr) and (Ba, Th)/(Nb) ratios. Sr isotopic enrichment is accompanied by an increase in these ratios. The least trace element enriched and most isotopically depleted fluids are from the high-Mg carbonatitic suite. Thus, HDFs could be derived from asthenospheric mantle as low degree melts that interact to varying degrees with an ancient, metasomatized, rutile- and phlogopite bearing, sub continental lithosphere mantle. The internal heterogeneity in the Sr isotopic ratios within a single diamond suite and even within single diamonds may indicate fluid-mixing processes. Such mixing may occur during migration through preferred mantle veins and may be affected by the small-scale geochemical variability within them.

  10. Hydrothermal versus active margin sediment supply to the eastern equatorial Pacific over the past 23 million years traced by radiogenic Pb isotopes: Paleoceanographic and paleoclimatic implications

    NASA Astrophysics Data System (ADS)

    Höfig, Tobias W.; Hoernle, Kaj; Hauff, Folkmar; Frank, Martin

    2016-10-01

    We investigated the evolution of the Pb isotopic composition of bulk sediments on the Cocos Plate in sedimentary successions of Deep Sea Drilling Project (DSDP) Site 495 and Ocean Drilling Program/Integrated Ocean Drilling Program (ODP/IODP) Site 1256 over the past 23 million years of depositional history. Our study addresses the relationship of the sediment Pb isotope record to plate tectonics, weathering inputs, and paleoceanography. It is the first effort to characterize the Pb isotopic evolution of eastern equatorial Pacific sedimentation covering the entire tectonic pathway of the Cocos Plate from its formation at the East Pacific Rise to its arrival at the Central American subduction zone. The Sites 495 and 1256 bulk sediment Pb isotope records are fully consistent over time despite distinct differences between the type of sediment deposited at both locations. A systematic and continuous trend from ∼23 to ∼6-4 Ma toward more radiogenic Pb isotopic compositions, e.g., 206Pb/204Pb ratios increase from 18.29 to 18.81, reflects a decrease in the contribution of hydrothermal particles from the East Pacific Rise and an increase in the predominantly eolian contribution of mixed weathering products from the continental arcs of the Northern and south Central Andes as well as from southern Mexico. Surprisingly, both the Pb isotopic composition of the detrital fraction and that of past seawater indicate that inputs from nearby Central America and the Galápagos Archipelago did not significantly contribute to the sediments of our core locations but were overwhelmed by other sediment sources. A systematic change to less radiogenic Pb isotope ratios in sediments younger than ∼4-3 Ma, reaching present-day 206Pb/204Pb values near 18.70, reflects a reduction of the continental input from the South Central Volcanic Zone of the Andean Arc and increased contributions from southern Mexican igneous complexes. This isotopic trend reversal took place as a consequence of

  11. Origin of adakite-like plutons in southern Korea

    NASA Astrophysics Data System (ADS)

    Oh, Jeong-Im; Choi, Sung Hi; Yi, Keewook

    2016-10-01

    We present Sr-Nd-Pb isotopic compositions for two adakite-like intrusions in southern Korea (Jindong and Bongnae), including major and trace element concentrations, and the sensitive high-resolution ion microprobe (SHRIMP) zircon U-Pb age. Our aim is to constrain the origin and tectonomagmatic processes that gave rise to the plutons. A SHRIMP U-Pb zircon age of 88.7 ± 0.7 Ma was obtained from a Jindong granodiorite sample. The Jindong plutons belong to the medium-K calc-alkaline series, and have an overall enrichment in large ion lithophile elements (LILE), such as K, Rb, Ba, and Pb, and a relative depletion in high field strength elements, such as Nb, Ta, and Ti, compared with the neighboring elements in the primitive mantle-normalized multi-trace element variation diagram. It was found that (87Sr/86Sr)i = 0.70475-0.70596, (143Nd/144Nd)i = 0.512547-0.512604, [(εNd)i = + 0.4 to 2.2], and (206Pb/204Pb)i = 18.19-18.37, which fall within the field of the arc-type Cretaceous to Tertiary Bulguksa intrusive rocks in the Sr-Nd and Pb-Pb isotopic correlation diagrams. The elevated Sr/Y (17-40), but low La/Yb (3.7-8.8) ratios of the Jindong plutons, together with their coherent geochemical trends and U-shaped rare earth element (REE) patterns, indicate that they were not formed by slab melting, but by amphibole-dominated fractional crystallization of the Bulguksa-like arc magma. A SHRIMP U-Pb zircon age of 226.5 ± 2.5 Ma was obtained from a Bongnae tonalite sample. The Bongnae plutons belong to the shoshonitic series. Their trace element patterns resemble the Jindong samples, but are characterized by significantly negative U anomalies in mafic rocks. They also have elevated MgO, Ni, Co, Cr, Rb, Ba, Sr, and low Al2O3 and Na2O contents at a given SiO2 concentration compared with the Jindong plutons, and are typified by highly radiogenic Sr and unradiogenic Nd and Pb isotopic compositions: [(87Sr/86Sr)i = 0.71096-0.71290, (143Nd/144Nd)i = 0.511641-0.511681, (εNd)i = - 13

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

    USGS Publications Warehouse

    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

  13. A Geochemical Transect Across the Lau and North Fiji Basins: New Evidence for the Distribution of Multiple Mantle Plume Components

    NASA Astrophysics Data System (ADS)

    Price, A. A.; Jackson, M. G.; Blichert-Toft, J.; Arculus, R. J.; Conatser, C. S.; Konter, J. G.; Koppers, A. A. P.; Blusztajn, J.

    2014-12-01

    The Lau and North Fiji backarc basins are located in a tectonically complex region of the South Pacific, where the upper mantle may have been modified by up to five hotspots (Samoa, Rurutu, Rarotonga, Macdonald, and Louisville), each with distinct geochemical fingerprints. We present new Hf, Nd, Sr, and Pb isotopic data for basaltic samples dredged from seven areas along an east-west transect spanning the Lau and North Fiji basins to determine the possible influence and distribution of these various hotspot sources. We find that the isotope ratios of nearly all samples can be explained by mixing a depleted mantle component, which is ubiquitous in the Lau Basin, with a component similar to that found in Samoan shield (EMII) and/or rejuvenated (EMI) lavas. Lavas as far southwest as the Fiji Triple Junction (North Fiji Basin) show enriched geochemical signatures (87Sr/86Sr and 206Pb/204Pb up to 0.7037 and 18.635 respectively, and 143Nd/144Nd and 176Hf/177Hf down to 0.51285 and 0.283023, respectively) trending toward Samoa. This observation extends the range of Samoan influence into the North Fiji Basin 400 km south of its previous observed extent at South Pandora Ridge. The few samples that cannot be explained solely by incorporation of Samoan material are from the northeastern Lau Basin (Falloon et al., 2007) and host a dilute HIMU component that may relate to the incorporation of material from the Rurutu hotspot. This component is not observed further to the west in the Lau and North Fiji basins. A ubiquitous EMI signature in the region may be linked to the Rarotonga hotspot. New dredges from the northeast Lau Basin may give clearer signals that will reveal the identity of the enriched plume component.

  14. Impact of Dust from Ore Processing Facilities on Rain Water Collection Tanks in a Tropical Environment--The Obvious Source "Ain't Necessarily So".

    PubMed

    Gulson, Brian; Korsch, Michael; Bradshaw, Anthony

    2016-02-01

    Concerns have been expressed that dust from the minerals processing facilities at Karumba Queensland Australia have resulted in elevated lead (Pb) concentrations in rain water tanks. The ores derived from the Century mine some 304 km from the port. High precision Pb isotopic measurements on environmental samples have been undertaken to evaluate the source of Pb in rainwaters and acid digests from roof wipes and gutter wipes. There does not appear to be any relationship between sample location and the processing facility but samples from the area subject to the prevailing winds show the highest contribution of Century Pb. All gutter wipes (82 to 1270 µg Pb/wipe) have contributions of Century ore ranging from 87% to 96%. The contribution of Century ore to five roof wipes (22 to 88 µg Pb/wipe) ranges from 89% to 97% and in the other two samples there is a mix of Century and Broken Hill Pb. Three of the seven rainwater have contributions of Century ore Pb ranging from 33% to 75%. Two of the other four rainwater samples have the highest water Pb concentrations of 88 and 100 µg/L and their isotopic data show Broken Hill Pb contributions ranging from 77% to 80%. The source of the Broken Hill Pb is probably from the galvanized roofing material and/or brass fittings in the rainwater tanks. The discrimination between various sources is only detectable using high precision (204)Pb-based isotopic ratios and not the now common inductively coupled plasma mass spectrometry (ICP-MS ) data presentations of the higher abundance isotopes (208)Pb, (207)Pb and (206)Pb. Isotopic results for the waters demonstrate that apportioning blame where there is an obvious point source may not always be the correct conclusion. Nevertheless the isotopic data for the gutter wipes indicates that there was widespread contamination from the processing facilities throughout the town. PMID:26907319

  15. Evolution of Mauna Kea Volcano, Hawaii: Petrologic and geochemical constraints on postshield volcanism

    SciTech Connect

    Frey, F.A.; Kennedy, A. ); Wise, W.S.; Kwon, S.T. ); Garcia, M.O.; West, H. )

    1990-02-10

    The postshield stage of volcano construction formed as the magma supply rate from the mantle decreased. The basaltic substage (Hamakua Volcanics) contains a diverse array of lava types including picrites, ankaramites, alkalic and tholeiitic basalt, and high Fe-Ti basalt. In contrast, the hawaiite substage (Laupahoehoe Volcanics) contains only evolved alkalic lavas, hawaiite, and mugearite; basalts are absent. Sr and Nd isotopic ratios for lavas from the two substages are similar, but there is a distinct compositional gap between the substages. The authors conclude that the petrogenetic processes forming the postshield lavas at Maina Kea and other Hawaiian volcanoes reflect movement of the volcano away from the hotspot. Specifically, they postulate the following sequence of events for postshield volcanism at Mauna Kea: (1) As the magma supply rate from the mantle decreased, major changes in volcanic plumbing occurred. The shallow magma chamber present during shield construction cooled and crystallized, and the fractures enabling magma ascent to the magma chamber closed. (2) Therefore subsequent basaltic magma ascending from the mantle stagnated within the lower crust, or perhaps at the crust-mantle boundary. Eruptions of basaltic magma ceased. (3) Continued volcanism was inhibited until basaltic magma in the lower crust cooled sufficiently to create relatively low-density, residual hawaiitic melts. Minor assimilation of MORB-related wall rocks, reflected by a trend toward lower {sup 206}Pb/{sup 204}/Pb in evolved postshield lavas, may have occurred at this time. A compositional gap developed because magma ascent was not possible until a low-density hawaiitic melt could escape from a largely crystalline mush.

  16. The provenance of ice-rafted debris in the glacial NE Atlantic: Ice sheet dynamics and global sea-level change during Heinrich event 4

    NASA Astrophysics Data System (ADS)

    Austin, William; Hibbert, Fiona; Leigh, Sasha; Ellam, Robert; Hodell, David

    2015-04-01

    The growth of the last British and Irish ice sheet (BIIS) through Marine Isotope Stage (MIS) 3 and its expansion onto and across the continental shelf of NW Scotland provides an excellent opportunity to test the relative contribution of BIIS ice-rafted debris (IRD) into Heinrich layers (HL ) adjacent to the European margin. Radiogenic isotope measurements of the sediments and quantification of the IRD components enable us to differentiate between geological source regions and provide a critical test of rapid, non-destructive mineral magnetic measurements which have been used to model sediment provenance through this interval. Within Greenland stadial (GS) 9 (approximately 40,120 - 38,360 yr ago) we recognize HL4 as a prominent, short-lived (ca. 200 yr) IRD event, characterized by a marked increase in the concentration of detrital carbonate grains with a diagnostic LIS δ18O fingerprint and decrease in the 206Pb/204Pb ratio and ɛNd(0) values of bulk sediments. A magnetic un-mixing model confirms that a Laurentide ice sheet (LIS)-sourced component dominates HL4 and that a BIIS-sourced component characterizes the latter part of GS9, increasing in relative abundance until the abrupt warming that marks the GS9 - Greenland interstadial (GI) 8 transition. The observed LIS-BIIS sequence, which we have replicated from cores MD95-2006 and MD04-2822, located 83 km apart in the northeastern North Atlantic, does not provide evidence of European "precursor" IRD events prior to HL4. Our results suggest that an extensive lobe of the BIIS extended onto the continental shelf of NW Europe during GS9 (ca. 38.5 kyr) and that an abrupt sea-level rise associated with the LIS-sourced component of HL4 triggered regional BIIS instability and collapse, with important implications for the relative timing of global sea-level change at this time.

  17. Chemical and isotopic studies of granitic Archean rocks, Owl Creek Mountains, Wyoming: Uranium-thorium-lead systematics of an Archean granite from the Owl Creek Mountains, Wyoming

    SciTech Connect

    Stuckless, J.S.; Nkomo, I.T.; Butt, K.A.

    1986-01-01

    Isotopic analyses of apparently unaltered whole-rock samples of a granite from the Owl Creek Mountains, Wyo., yield a lead-lead isochron age of 2730 {plus minus} 35 Ma, which is somewhat older than the age obtained by the rubidium-strontium whole-rock method. Thorium-lead data for the same samples deviate markedly from an isochronal relation; however, calculated initial {sup 208}Pb/{sup 204}Pb ratios correlate with whole-rock {delta}{sup 18}O values and lead to the conclusion that the {sup 232}Th-{sup 208}Pb data are not colinear because of an originally heterogeneous granitic magma. Relationships in the {sup 207}Pb/{sup 235}U-{sup 206}Pb/{sup 238}U system show that uranium was mobilized during early Laramide time or shortly before, such that most surface and shallow drill-core samples lost 60-80 percent of their uranium, and some fractured, deeper drill-core samples gained from 50 to 10,000 percent uranium. Fission-track maps show that much uranium is located along edges and cleavages of biotite and magnetic where it is readily accessible to oxidizing ground water. Furthermore, qualitative comparisons of uranium distribution in samples with excess radiogenic lead and in samples with approximately equilibrium amounts of uranium and lead suggest that the latter contain more uranium in these readily accessible sites. Unlike other granites that have uranium distributions and isotopic systematics similar to those observed in this study, the granite of the Owl Creek Mountains is not associated with economic uranium deposits.

  18. Impact of Dust from Ore Processing Facilities on Rain Water Collection Tanks in a Tropical Environment--The Obvious Source "Ain't Necessarily So".

    PubMed

    Gulson, Brian; Korsch, Michael; Bradshaw, Anthony

    2016-02-22

    Concerns have been expressed that dust from the minerals processing facilities at Karumba Queensland Australia have resulted in elevated lead (Pb) concentrations in rain water tanks. The ores derived from the Century mine some 304 km from the port. High precision Pb isotopic measurements on environmental samples have been undertaken to evaluate the source of Pb in rainwaters and acid digests from roof wipes and gutter wipes. There does not appear to be any relationship between sample location and the processing facility but samples from the area subject to the prevailing winds show the highest contribution of Century Pb. All gutter wipes (82 to 1270 µg Pb/wipe) have contributions of Century ore ranging from 87% to 96%. The contribution of Century ore to five roof wipes (22 to 88 µg Pb/wipe) ranges from 89% to 97% and in the other two samples there is a mix of Century and Broken Hill Pb. Three of the seven rainwater have contributions of Century ore Pb ranging from 33% to 75%. Two of the other four rainwater samples have the highest water Pb concentrations of 88 and 100 µg/L and their isotopic data show Broken Hill Pb contributions ranging from 77% to 80%. The source of the Broken Hill Pb is probably from the galvanized roofing material and/or brass fittings in the rainwater tanks. The discrimination between various sources is only detectable using high precision (204)Pb-based isotopic ratios and not the now common inductively coupled plasma mass spectrometry (ICP-MS ) data presentations of the higher abundance isotopes (208)Pb, (207)Pb and (206)Pb. Isotopic results for the waters demonstrate that apportioning blame where there is an obvious point source may not always be the correct conclusion. Nevertheless the isotopic data for the gutter wipes indicates that there was widespread contamination from the processing facilities throughout the town.

  19. The size of plume heterogeneities constrained by Marquesas isotopic stripes

    NASA Astrophysics Data System (ADS)

    Chauvel, Catherine; Maury, René C.; Blais, Sylvain; Lewin, Eric; Guillou, Hervé; Guille, GéRard; Rossi, Philippe; Gutscher, Marc-André

    2012-07-01

    The scale and geometry of chemical and isotopic heterogeneities in the source of plumes have important scientific implications on the nature, composition and origin of plumes and on the dynamics of mantle mixing over time. Here, we address these issues through the study of Marquesas Islands, one of the Archipelagoes in Polynesia. We present new Sr, Nd, Pb, Hf isotopes as well as trace element data on lavas from several Marquesas Islands and demonstrate that this archipelago consists of two adjacent and distinct rows of islands with significantly different isotopic compositions. For the entire 5.5 Ma construction period, the northern islands, hereafter called the Ua Huka group, has had systematically higher 87Sr/86Sr and lower 206Pb/204Pb ratios than the southern Fatu Hiva group at any given 143Nd/144Nd value. The shape and curvature of mixing arrays preclude the ambient depleted MORB mantle as one of the mixing end-members. We believe therefore that the entire isotopic heterogeneity originates in the plume itself. We suggest that the two Marquesas isotopic stripes originate from partial melting of two adjacent filaments contained in small plumes or "plumelets" that came from a large dome structure located deep in the mantle under Polynesia. Low-degree partial melting under Marquesas and other "weak" Polynesian hot spot chains (Pitcairn-Gambier, Austral-Cook, Society) sample small areas of the dome and preserve source heterogeneities. In contrast, more productive hot spots build up large islands such as Big Island in Hawaii or Réunion Island, and the higher degrees of melting blur the isotopic variability of the plume source.

  20. U-Th-Pb and Rb-Sr systematics of Apollo 17 boulder 7 from the North Massif of the Taurus-Littrow Valley

    USGS Publications Warehouse

    Nunes, P.D.; Tatsumoto, M.; Unruh, D.M.

    1974-01-01

    Portions of highland breccia boulder 7 collected during the Apollo 17 mission were studied using UThPb and RbSr systematics. A RbSr internal isochron age of 3.89 ?? 0.08 b.y. with an initial 87Sr/86Sr of 0.69926 ?? 0.00008 was obtained for clast 1 (77135,57) (a troctolitic microbreccia). A troctolitic portion of microbreccia clast 77215,37 yielded a UPb internal isochron of 3.8 ?? 0.2 b.y. and an initial 206Pb/207Pb of 0.69. These internal isochron age are interpreted as reflecting metamorphic events, probably related to impacts, which reset RbSr and UPb mineral systems of older rocks. Six portions of boulder 7 were analyzed for U, Th, and Pb as whole rocks. Two chemical groups appear to be defined by the U, Th, and Pb concentration data. Chemical group A is characterized by U, Th, and Pb concentrations and 238U/204Pb values which are higher than those of group B. Group A rocks have typical 232Th/238U ratios of ??? 3.85, whereas-group B rocks have unusually high Th/U values of ??? 4.1. Whole-rock UPb and PbPb ages are nearly concordant. Two events appear to be reflected in these data - one at ??? 4.4 b.y. and one at ??? 4.5 b.y. The chemical groupings show no correlation with documented ages. The old ages of ??? 4.4 b.y. and ??? 4.5 b.y. may, like the younger ??? 4.0 b.y. ages, be related to basin excavation events. ?? 1974.

  1. Dissolved lead in the deep Southeast Pacific Ocean: results of the 2013 US GEOTRACES cruise

    NASA Astrophysics Data System (ADS)

    Boyle, E. A.; Lee, J. M.; Zhang, J.; Echegoyen, Y.

    2014-12-01

    Lead (Pb) in the modern ocean is dominated by anthropogenic Pb, which has been evidenced by highly elevated seawater Pb concentrations and Pb stable isotope ratios (204Pb, 206Pb, 207Pb, and 208Pb) altered from pre-anthropogenic values. A number of studies have shown the human impact on oceanic Pb in many parts of the world ocean, but little Pb data has been available for the Southeast Pacific Ocean. In this presentation, we will show the dissolved Pb (<0.2µm) results from the US GEOTRACES cruise in October - December 2013, which sailed from Manta, Ecuador, to Tahiti along around 12 degrees south. Dissolved Pb concentrations from all 36 surface stations and deep (>1000m) Pb profiles from 18 stations will be presented, and the results will be also compared to our unpublished data from the BiG RAPA cruise in 2010, whose cruise track from Arica, Peru, to Easter Island is slightly south of the US GEOTRACES cruise. The BiG RAPA data showed that dissolved Pb concentrations of the southeast Pacific Ocean are relatively low, varying in the range of 8-20 pmol/kg at the surface with a slight maximum (14-22 pmol/kg) at around 400m depth, and 2-10 pmol/kg in deep waters below 1000m depth. The Pb concentrations were found to be higher at a marginal station off Peru, reaching 45 pmol/kg at the surface and 65 pmol/kg in the subsurface maximum at 150m depth, and varying between 17 and 23 pmol/kg in deep waters. Our dataset, along with the results from the BiG RAPA cruise, will provide the first overview on the dissolved Pb distribution of the southeast Pacific Ocean, which will further our understanding on the human impact on the global ocean.

  2. Impact of Dust from Ore Processing Facilities on Rain Water Collection Tanks in a Tropical Environment—The Obvious Source “Ain’t Necessarily So”

    PubMed Central

    Gulson, Brian; Korsch, Michael; Bradshaw, Anthony

    2016-01-01

    Concerns have been expressed that dust from the minerals processing facilities at Karumba Queensland Australia have resulted in elevated lead (Pb) concentrations in rain water tanks. The ores derived from the Century mine some 304 km from the port. High precision Pb isotopic measurements on environmental samples have been undertaken to evaluate the source of Pb in rainwaters and acid digests from roof wipes and gutter wipes. There does not appear to be any relationship between sample location and the processing facility but samples from the area subject to the prevailing winds show the highest contribution of Century Pb. All gutter wipes (82 to 1270 µg Pb/wipe) have contributions of Century ore ranging from 87% to 96%. The contribution of Century ore to five roof wipes (22 to 88 µg Pb/wipe) ranges from 89% to 97% and in the other two samples there is a mix of Century and Broken Hill Pb. Three of the seven rainwater have contributions of Century ore Pb ranging from 33% to 75%. Two of the other four rainwater samples have the highest water Pb concentrations of 88 and 100 µg/L and their isotopic data show Broken Hill Pb contributions ranging from 77% to 80%. The source of the Broken Hill Pb is probably from the galvanized roofing material and/or brass fittings in the rainwater tanks. The discrimination between various sources is only detectable using high precision 204Pb-based isotopic ratios and not the now common inductively coupled plasma mass spectrometry (ICP-MS ) data presentations of the higher abundance isotopes 208Pb, 207Pb and 206Pb. Isotopic results for the waters demonstrate that apportioning blame where there is an obvious point source may not always be the correct conclusion. Nevertheless the isotopic data for the gutter wipes indicates that there was widespread contamination from the processing facilities throughout the town. PMID:26907319

  3. Sr, Nd and Pb Isotope Geochemistry of Near-ridge Seamounts in Eastern Pacific: Implications for Upper Mantle Composition and EPR Magmatic Segmentation

    NASA Astrophysics Data System (ADS)

    Castillo, P. R.; White, W. M.; Batiza, R.

    2005-12-01

    Near-ridge seamount lavas tend to reflect the true composition of the upper mantle source of MORB because these are generated by relatively smaller degrees of melting of smaller volumes of the mantle compared to nearby axial lavas; they also by-pass the axial chamber mixing and fractionation processes that are responsible for the relatively more uniform chemical and isotopic composition of normal-MORB. New Sr, Nd and Pb isotope data combined with published data for lavas from near-ridge seamounts on either side of the EPR segment between the 11o45' OSC and Orozco Transform at 15o00' show latitudinal isotopic variation very similar to that shown by the rise axial lavas (Castillo et al., G3 1, 1999). Seamount and axial lavas at both ends of the rise segment have on average slightly higher and more limited range of 143Nd/144Nd, but slightly lower 206Pb/204Pb and 87Sr/86Sr ratios than lavas at the center of the segment. Some of the seamounts are located on ~8 Ma rise flank crust although most of the seamount lavas are fairly young (e.g., lavas from Seamount 6 on ~3 Ma crust are only 3 to 900 kyr - Graham et al., Nature 326, 1987). Thus near-ridge seamount isotope data provide the first documentation for a large-scale (~350 km long x ~720 km wide), systematic compositional variation of the upper mantle source of EPR MORB. Such a scale of variation is larger and longer than the size and <1 myr life span of the majority of non-transform offsets, which are supposed to be responsible for the along-axis compositional variations of EPR MORB according to the "bottoms up" model of magmatic segmentation.

  4. Pb - Isotopes and Pulses of the Deccan Plume

    NASA Astrophysics Data System (ADS)

    Basu, A. R.; Yannopoulos, A. S.

    2015-12-01

    Mantle plumes are generally implicated for flood basalt generation in both continental and oceanic environments by impact of large plume heads beneath or within the lithosphere. The Deccan and Siberian flood basalt eruptions, synchronous with the Cretaceous-Paleogene and end-Permian extinctions, respectively, continue to fascinate geoscientists in search for the "kill-mechanisms" by impacts, volcanisms or both. Recently, Richards et al. (2015) proposed that bulk of the Deccan eruption was triggered by the Chicxulub impact. We showed (Basu et al., 1993) that early (68.5 Ma) and late (65 Ma) alkalic pulses of the Deccan were before and after the impact event at 66 Ma. Here, we focus on an extensive volcano-stratigraphic study of Pb isotopic systematics of 69 basaltic samples from 3 subgroups and 12 formations of the Deccan, each sampled from bottom to top along the stratigraphic section, covering the 3km thick 12 Deccan formations. Pb is sensitive to crustal contamination of mantle plume-derived magmas as both the upper and lower mantle are low in Pb (0.02 - 0.15 ppm) compared to ~ 4 ppm in continental crust. The lower Deccan formations of Kalsubai and Lonavala have initial 206Pb/204Pb with a widely varying range (16.543 - 22.823) indicating continental crustal contamination. In contrast, the upper formations of the Wai subgroup show a narrow range of 16.883 to 18.956, reflecting the plume signature. In addition, the 206Pb/204Pb and 207Pb/204Pb data of the Kalsubai subgroup lavas give an isochron age of 2603±140 Ma (single-stage, µ = 8). The Wai subgroup shows a narrow and restricted Pb isotopic range plotting closer to the Geochron. We interpret these data to infer that the basement rocks of the Deccan, the Archean Indian craton, were assimilated by the upwelling melt, ultimately clearing the conduit passages for the lavas sourced from direct melting of the plume head.

  5. LA-MC-ICPMS Pb Pb dating of rutile from slowly cooled granulites: Confirmation of the high closure temperature for Pb diffusion in rutile

    NASA Astrophysics Data System (ADS)

    Vry, Julie K.; Baker, Joel A.

    2006-04-01

    Rapid Pb-Pb dating of natural rutile crystals by laser ablation multiple-collector inductively coupled plasma mass spectrometry (LA-MC-ICPMS) is investigated as a tool for constraining geological temperature-time histories. LA-MC-ICPMS was used to analyse Pb isotopes in rutile from granulite-facies rocks from the Reynolds Range, Northern Territory, Australia. The resultant ages were compared with previous U-Pb zircon and monazite age determinations and new mica (muscovite, phlogopite, and biotite) Rb-Sr ages from the same metamorphic terrane. Rutile crystals ranging in size from 3.5 to 0.05 mm with ⩽20 ppm Pb were ablated with a 300-25 μm diameter laser beam. Crystals larger than 0.5 mm yielded sufficiently precise 206Pb/ 204Pb and 207Pb/ 204Pb ratios to correct for the presence of common Pb, and individual rutile crystals often exhibited sufficient Pb isotopic heterogeneity to allow isochron calculations to be performed on replicate analyses of a single crystal. The mean of 12 isochron ages is 1544 ± 8 Ma (2 SD), with isochron ages for single crystals having uncertainties as low as ±1.3 Myr (2 SD). The 207Pb- 206Pb ages calculated without correction for common Pb are typically <0.5% higher than the common-Pb-corrected isochron ages reflecting the very minor amounts of common Pb present in the rutile. The LA-MC-ICPMS method described samples only the outer 0.1-0.2 mm of the rutile crystals, resulting in a grain size-independent apparent closure temperature ( Tc) for Pb diffusion in rutile that is less than the Tc of monazite ⩽0.1 mm in diameter, but significantly higher than the Rb-Sr system in muscovite (550 °C), phlogopite (435 °C) and biotite (400 °C). Even small rutile crystals are extremely resistant to isotopic resetting. For the established slow cooling rate of ca. 3 °C/Myr, the Tc for Pb diffusion in the analysed rutile is ca. 630 °C. This is in excellent agreement with recent experimental results that indicate that rutile has a higher Tc than

  6. Sources and Spatial Distribution of Metal Pollutants in Soils near the El Paso Smelter: A Forensic Study with Pb and Pu Isotopes.

    NASA Astrophysics Data System (ADS)

    Ketterer, Michael; Moan, Matthew; Gremillion, Paul

    2010-05-01

    Lead and copper smelting has been conducted at El Paso since the late 1800's, and as a result, environmental media near the smelter have become contaminated. A study has been conducted to investigate the sources and spatial distribution of metal pollutants (Pb, Cd, Zn, Hg, As, Cu) and concomitant tracers (Ag, In, Sb, Bi) in soils from the smelter vicinity. Sampled locations were residential and non-residential locations in El Paso (Texas, USA), Anapra (New Mexico, USA) and Ciudad Juarez (Chihuahua, Mexico). Lead isotope studies indicate that the soil Pb is derived from smelting, and is consistent with two-component mixing between lead ores from Chihuahua (northern Mexico) having 206Pb/204Pb of 18.6 - 18.8 and ores from the Hanover, New Mexico (USA) mining district with 206Pb/204Pb of ~ 17.6. The Pb isotope results also exclude other common anthropogenic Pb sources such as paint and gasoline emissions as being major contributors. Concentrations of Hg and Pb of up to 10 and 11,000 ppm were found in surface soils within 1 km of the smelter. The metal concentration results clearly indicate that soils near the smelter (< 5 km) exhibit much higher concentrations of smelter-related elements than do soils from control locations (> 10 km distant). A general trend of decreasing concentrations vs. distance from the smelter was also observed. However, the results indicate that metal concentrations vary widely even at a fixed distance from the smelter point source. This phenomenon results from a combination of natural and anthropogenic processes that disturb and re-distribute soils in the surface environment. The site conditions consist of a very arid environment with little vegetation cover that is frequently disturbed by high winds and severe episodic rainfall. To study these effects, we have investigated stratospheric fallout plutonium (239+240Pu) as a proxy measure of disturbed vs. undisturbed soil conditions. The premise is that 'undisturbed' locations will have high 239

  7. Origin of enriched ocean ridge basalts and implications for mantle dynamics

    NASA Astrophysics Data System (ADS)

    Donnelly, Kathleen E.; Goldstein, Steven L.; Langmuir, Charles H.; Spiegelman, Marc

    2004-10-01

    The Mid-Atlantic Ridge (MAR) south of the Kane Fracture Zone at ˜23°N (the MARK area) is distant from hot spots and a type area for "normal" mid-ocean ridge basalt (N-MORB) depleted in highly incompatible elements. High-density sampling reveals that a small proportion of basalt are enriched in incompatible elements (enriched mid-ocean ridge basalts, E-MORB) from the MARK area. It is apparent that enriched magma sources, not associated with hot spots, are widespread in the upper mantle and are a common occurrence on both fast- and slow-spreading ridges. Evaluation of the trace-element systematics shows that E-MORB generation requires two stages. Low-degree melts metasomatise the upper mantle to create an enriched source, which later undergoes large extents of melting. A significant time lapse between the two events is required by differences in radiogenic isotope ratios. Atlantic, Pacific, and Indian ocean ridges that are far from hot spots show "mantle isochron" ages of ˜300 Ma for the Sm-Nd, Rb-Sr, and 238U- 206Pb systems after corrections for melting, but these ages need not be indicative of a specific event. Instead, they can result from continuous processes of formation and destruction of enriched mantle sources by melting and convective mixing. A two-box model describing these processes illuminates relationships between mantle isochron ages and upper mantle dynamics. If formation-destruction of enriched mantle is at steady state, constant "mantle isochron" ages are maintained and depend on the residence time of enriched mantle sources, the half-life of the radioactive system, and the daughter element behavior during mantle melting. The common ages of the Sr, Nd, and Pb systems reflects their long half-lives and similar melting behavior. In contrast, 207Pb/ 204Pb- 206Pb/ 204Pb ages are approximately twice as old due to the short half-life of 235U relative to the age of the Earth. For the long-lived systems, the mantle isochron ages approximate the residence

  8. Magma types and mantle sources of the Bárðarbunga volcanic system, Iceland

    NASA Astrophysics Data System (ADS)

    Halldórsson, Sæmundur; Rubin, Ken; Sverrisdóttir, Guðrún; Sigurðsson, Gylfi

    2015-04-01

    , Holocene lavas from the Veiðivötn fissure swarm lie on two parallel trends, with 206Pb/204Pb ratios >18.40. In contrast, subglacial formations in the Dyngjuháls region, form a single trend with 206Pb/204Pb always <18.39. Significantly, another group of young lavas fall right in-between the three trends: those from the new fissure lava north of Dyngjujökull, historical Veiðivötn fissure swarm lavas, and Holocene Dyngjuháls lavas. In sharp contrast, samples of unknown age from the ice-free part of the Bárðarbunga volcano display significant heterogeneity and overlap all of these data/trends. We propose that at least three mantle components contribute melts to the BVS, in different proportions in space and time. However, recent eruptions, regardless of location appear to be fed from the same or at least a more uniform magma source. Finally, we note that removal of ~2500 m. of glacial ice that overlaid the BVS during the last deglaciation, could have strongly influenced the melting regime in addition to magma delivery and/or storage under central Iceland - much more so than along the Northern rift zone (e.g., Theistareykir; Slater et al. 1998). Slater, L., Jull, M., McKenzie, D., Grönvold, K., 1998. Deglaciation effects on mantle melting beneath Iceland: Results from the northern volcanic zone. Earth Planet. Sci. Lett. 164, 151-164.

  9. The influence of melt flux and crustal processing on Re-Os isotope systematics of ocean island basalts: Constraints from Galápagos

    NASA Astrophysics Data System (ADS)

    Gibson, S. A.; Dale, C. W.; Geist, D. J.; Day, J. A.; Brügmann, G.; Harpp, K. S.

    2016-09-01

    New rhenium-osmium data for high-MgO (>9 wt.%) basalts from the Galápagos Archipelago reveal a large variation in 187Os/188Os (0.1304 to 0.173), comparable with the range shown by primitive global ocean island basalts (OIBs). Basalts with the least radiogenic 187Os/188Os occur closest to the Galápagos plume stem: those in western Galápagos have low 187Os/188Os, moderate 87Sr/86Sr, 143Nd/144Nd, 206Pb/204Pb and high 3He/4He whereas basalts in the south also have low 187Os/188Os but more radiogenic 87Sr/86Sr, 143Nd/144Nd, 206Pb/204Pb and 3He/4He. Our new Os isotope data are consistent with the previously established spatial zonation of the common global isotopic mantle reservoir "C" and ancient recycled oceanic crust in the mantle plume beneath western and southern parts of Galápagos, respectively. Galápagos basalts with the most radiogenic 187Os/188Os (up to 0.1875) typically have moderate MgO (7-9 wt.%) and low Os (<50 pg g-1) but have contrastingly unenriched Sr, Nd and Pb isotope signatures. We interpret this decoupling of chalcophile and lithophile isotopic systems as due to assimilation of young Pacific lower crust during crystal fractionation. Mixing models show the assimilated crust must have higher contents of Re and Os, and more radiogenic 187Os/188Os (0.32), than previously proposed for oceanic gabbros. We suggest the inferred, exceptionally-high radiogenic 187Os of the Pacific crust may be localised and due to sulfides precipitated from hydrothermal systems established at the Galápagos Spreading Centre. High 187Os/188Os Galápagos basalts are found where plume material is being dispersed laterally away from the plume stem to the adjacent spreading centre (i.e. in central and NE parts of the archipelago). The extent to which crustal processing influences 187Os/188Os appears to be primarily controlled by melt flux: as distance from the stem of the Galápagos plume increases, the melt flux decreases and crustal assimilation becomes proportionally

  10. Linking serpentinite geochemistry with tectonic evolution at the subduction plate-interface: The Voltri Massif case study (Ligurian Western Alps, Italy)

    NASA Astrophysics Data System (ADS)

    Cannaò, E.; Scambelluri, M.; Agostini, S.; Tonarini, S.; Godard, M.

    2016-10-01

    Recent geochemical work shows that subduction-zone serpentinites are repositories for fluid-mobile elements absorbed during interaction with sediment-derived fluids. Unraveling the geochemical fingerprint of these rocks helps to define timing of tectonic accretion of sediments along the subduction interface and the role of serpentinite in element recycling to volcanic arcs. Here we present the trace element and isotopic composition (B-O-H, Sr, Pb) of high-pressure serpentinites from the Voltri Massif (Ligurian Western Alps, Italy), to discuss their role as incompatible element carriers and their contribution to recycling of sediment-derived components in subduction zones. The serpentinites presented here record metamorphic olivine growth during eclogite-facies metamorphism and show undeformed and mylonitic textures. Field relations show that undeformed rocks are enclosed in deformed ones and that no metasedimentary rocks are present nearby. Undeformed serpentinite has very high δ11BSRM951 (from +26‰ to +30‰), low Sr and Pb isotope ratios (87Sr/86Sr = 0.7053-0.7069; 206Pb/204Pb = 18.131-18.205) and low As and Sb contents (0.1 and 0.01 μg/g, respectively). Oxygen and hydrogen isotope compositions are +4.5‰ and -67‰, respectively. In contrast, mylonitic serpentinite shows lower δ11B (from +22‰ to +17‰), significant enrichment in radiogenic Sr and Pb isotopes (87Sr/86Sr up to 0.7105; 206Pb/204Pb up to 18.725), and enrichment in As and Sb (1.3 and 0.39 μg/g, respectively). δ18O of the mylonitic serpentinites reaches values of +5.9‰, whereas δD is comparable with that of undeformed rocks (approximately -70‰). In mylonitic serpentinites, the B and Sr isotopic values and the fluid-mobile element (FME) concentrations are near those for the Voltri metasedimentary rocks (calc- and mica-schists). Pb systematics also reveal influx of a crust-derived component. Our dataset shows that undeformed serpentinite still preserves an oceanic geochemical fingerprint

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

    USGS Publications Warehouse

    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

  12. Origin of andesitic rocks: Geochemical constraints from Mesozoic volcanics in the Luzong basin, South China

    NASA Astrophysics Data System (ADS)

    Chen, Long; Zhao, Zi-Fu; Zheng, Yong-Fei

    2014-03-01

    A combined study of whole-rock major-trace elements and Sr-Nd-Pb-Hf isotopes as well as zircon U-Pb ages and Hf-O isotopes was carried out for Mesozoic andesitic-basaltic volcanics from the Luzong basin in the Middle-Lower Yangtze River Belt, South China. The results provide insights into the origin of mantle sources above fossil Andes-type oceanic subduction zone and thus into the petrogenesis of andesitic rocks on fossil and modern continental margins. These volcanics are primarily composed of basaltic trachyandesite and trachyandesite, with small amounts of trachybasalt and trachyte. They exhibit variable contents of SiO2 (48.66-63.43 wt.%), MgO (0.39-4.85 wt.%), Na2O (1.22-6.07 wt.%) and K2O (2.53-10.10 wt.%), with highly variable K2O/Na2O ratios from 0.45 to 7.39. They are characterized by arc-like trace element distribution patterns, with significant enrichment of LILE, Pb and LREE but depletion of HFSE. They exhibit relatively enriched Sr-Nd-Pb-Hf isotope compositions, with initial 87Sr/86Sr ratios of 0.7050 to 0.7066, negative ɛNd(t) values of - 8.0 to - 3.1, negative ɛHf(t) values of - 11.1 to - 1.1, and elevated 207Pb/204Pb and 208Pb/204Pb ratios at given 206Pb/204Pb ratios. Zircon U-Pb dating yields consistent ages of 127 ± 2 to 137 ± 1 Ma for magma emplacement through volcanic eruption. The zircon exhibits slightly high δ18O values of 5.3 to 7.6‰ and variable ɛHf(t) values of - 13.1 to 2.6. An integrated interpretation of all these geochemical data leads to the conclusion that the Luzong andesitic-basaltic volcanics were primarily derived from partial melting of fertile and enriched, mafic-ultramafic mantle sources that are similar to those of continental arc andesites. Such mantle sources are hypothesized to form by reaction of the mantle wedge peridotite not only with hydrous felsic melts derived from partial melting of seafloor sediment but also with aqueous fluid derived from metamorphic dehydration of altered oceanic basalt during

  13. Geology, isotope geochemistry and geochronology of the Jinshachang carbonate-hosted Pb-Zn deposit, southwest China

    NASA Astrophysics Data System (ADS)

    Zhou, Jia-Xi; Bai, Jun-Hao; Huang, Zhi-Long; Zhu, Dan; Yan, Zai-Fei; Lv, Zhi-Cheng

    2015-02-01

    The Jinshachang Pb-Zn deposit, an exceptionally radiogenic Pb-enriched sulfide deposit, hosted by dolostone of the Upper Sinian (Neoproterozoic) Dengying Formation and the Lower Cambrian Meishucun Formation, is located in the western Yangtze Block, about 300 km northeast of Kunming city in southwest China. Ore bodies in this deposit are dominated by strata-bound type and steeply dipping vein type. Primary ores in these two types are composed of sphalerite, galena, fluorite, barite and quartz with massive, banded, veined and disseminated structures. Twenty-seven ore bodies in the Jinshachang deposit host 4.6 million tons of sulfide ores at average grades of 4.07 wt.% Pb and 5.03 wt.% Zn. Quartz separates from the sulfide ores have δDH2O values ranging from -137‰ to -86.2‰ with an average of -114‰ (n = 7), lower than those of magmatic, metamorphic and meteoric water, suggesting a contribution of organic water. δ34SCDT values of ninety-one sulfide separates range from +1.1‰ to +13.4‰ with an average of +5.7‰, lower than those of evaporites (δ34SCDT = +15‰ to +35‰) in the Cambrian to Triassic sedimentary strata in NE Yunnan province. δ34SCDT values of eight barite separates range from +32‰ to +35‰ (average +34‰), within the range of evaporites. These data suggest that S2- in the hydrothermal fluids derived from evaporites by thermo-chemical sulfate reduction (TSR), whereas SO42- directly originated from the evaporites. Six sulfide separates have highly radiogenic 206Pb/204Pb ratios ranging from 20.74 to 21.18 (average 20.92), 207Pb/204Pb ratios ranging from 15.85 to 15.89 (average 15.87), and 208Pb/204Pb ratios ranging from 40.89 to 41.42 (average 41.16). The Pb isotopes of the sulfides plot above the upper crust Pb average evolution curve and overlap the Cambrian sedimentary rocks, but are different from the Sinian dolostone. This indicates a crustal source of Pb most likely derived from the Cambrian sedimentary rocks. The initial 87Sr/86Sr

  14. Characterization and component tracing of Banded Iron Formations deposited during the ~2.7 Ga superplume event: An example from the Tati Greenstone Belt, Northeastern Botswana

    NASA Astrophysics Data System (ADS)

    Døssing, L. N.; Frei, R.; Stendal, H.; Mapeo, R. B.

    2008-12-01

    , but variable 207Pb/204Pb relative to 206Pb/204Pb ratios of BIFs are indicative of a high-μ (238U/204Pb) prehistory of their source materials which, in accordance with Nd model ages defined by the BIFs, can best be modeled by a 3.0 - 3.2 Ga extraction of these sources from a depleted mantle reservoir. Sm-Nd isotopic relationships between silica (SiO2)- and iron (Fe2O3)-rich mesobands of one of the studied BIFs point to essentially two REY sources controlling the depositional environment. The first is characterized by elevated Sm-Nd ratios and a negative inferred ɛNd(2.7 Ga) value of -2.5 and is associated with high Fe fluxes. The second source, associated with high Si fluxes, is instead characterized by lower Sm-Nd ratios and a slightly positive inferred ɛNd(2.7 Ga) value of +0.4. While the association of high Fe concentrations and elevated Sm-Nd in BIF mesobands is characteristic of a hydrothermal seawater input, the Sm-Nd isotopic characterization of this source, unlike other Archean BIFs, points to a significantly LREE enriched (rather than depleted) mantle source. This finding is compatible with the potential existence of a subcontinental lithospheric mantle reservoir beneath the Zimbabwe and Kaapvaal craton.

  15. 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:

    USGS Publications Warehouse

    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.

  16. Lead and strontium isotope data for thermal waters of the regional geothermal system in the Twin Falls and Oakley areas, South-Central Idaho

    SciTech Connect

    Mariner, R.H.; Young, H.W.

    1995-12-31

    Thermal fluids obviously related to aquifers in both rhyolite and limestone occur in the Twin Falls-Oakley area of south-central Idaho. Limestone-related waters (high calcium with low silica and fluoride) occur in the middle and upper (southern) parts of the area. Rhyolite-related waters (low calcium but high in silica and fluoride) occur in the lower (northern) part of the area. The relation of thermal fluids in Paleozoic limestone to thermal fluids in Tertiary rhyolite is unknown. Thermal fluids from limestone are dilute, so water-rock reaction in rhyolite could obliterate chemical evidence of fluid residence in a limestone. However, isotopic tracers such as {sup 206}Pb/{sup 204}Pb, {sup 207}Pb/{sup 204}Pb, {sup 208}Pb/{sup 204}Pb, and {sup 87}Sr/{sup 86}Sr might preserve evidence of fluid residence in limestone. Systematic relations between these isotopes and dissolved constituents in the water demonstrate the presence of limestone beneath most if not all of the study area and that aquifers in the limestone and rhyolite are hydrologically connected.

  17. Lead concentration and isotopic composition in five peridotite inclusions of probable mantle origin

    USGS Publications Warehouse

    Zartman, R.E.; Tera, F.

    1973-01-01

    The lead content of five whole-rock peridotite inclusions (four lherzolites and one harzburgite) in alkali basalt ranges from 82 to 570 ppb (parts per billion). Approximately 30-60 ppb of this amount can be accounted for by analyzed major silicate minerals (olivine ??? 10 ppb; enstatite 5-28 ppb; chrome diopside ???400 ppb). Through a series of acid leaching experiments, the remainder of the lead is shown to be quite labile and to reside in either glassy or microcrystalline veinlets or accessory mineral phases, such as apatite and mica. The lead isotopic composition of the peridotites (206Pb/204Pb = 18.01-18.90; 207Pb/204Pb = 15.52-15.61; 208Pb/204Pb = 37.80-38.86) lies within the range of values defined by many modern volcanic rocks and, in particular, is essentially coextensive with the abyssal tholeiite field. In all but one instance, isotopic differences were found between the peridotite and its host alkali basalt. Two of the peridotites clearly demonstrated internal isotopic heterogeneity between leachable and residual fractions that could not simply be due to contamination by the host basalt. However, there is no evidence that these ultramafic rocks form some layer in the mantle with isotopic characteristics fundamentally different from those of the magma sources of volcanic rocks. ?? 1973.

  18. Pb isotope composition in lichens and aerosols from eastern Sicily: Insights into the regional impact of volcanoes on the environment

    SciTech Connect

    Monna, F. ); Aiuppa, A.; Varrica, D. ); Dongarra, G. CNR, Palermo . Istituto Geochimica dei Fluidi)

    1999-08-01

    A total of 25 lichen thalli of Parmelia conspersa (Ehrh), collected at Vulcano island and at Mt. Etna, during a one-year biogeochemical survey, were analyzed for Pb, br, Al, Sc,[sup 206]Pb/[sup 207]Pb, and [sup 208]Pb/[sup 206]Pb ratios. Lead isotope ratios were also measured on aerosol samples from urban areas and industrial sites of Sicily. The observed [sup 206]Pb/[sup 207]Pb range for urban and industrial aerosols matches the anthropogenic signature. Lichens instead, are closer to the compositional field of [sup 206]Pb rich geogenic sources. This natural input is more evident at Vulcano island than at Mt. Etna, where the anthropogenic activities are considerably more effective. On the basis of lead isotope data, Pb/Br ratios and calculated lead enrichment factors, a natural lead pollution from volcanoes is suggested. Volcanic lead contribution ranges from 10 to 30% at Mt. Etna to 10--80% at Vulcano island.

  19. Petrology of the Guenfalabo ring-complex: An example of a complete series along the Cameroon Volcanic Line (CVL), Cameroon

    NASA Astrophysics Data System (ADS)

    Donald Ngonge, E.; Hollanda, Maria Helena B. M.; Nsifa, E. Nkonguin; Tchoua, Felix M.

    2014-08-01

    In the Guenfalabo ring-complex (GRC), two non-comagmatic rock suites have been identified as a result of two volcanic episodes: Suite 1 (68.8 ± 1.7 Ma by K/Ar on trachyte) of peralkaline trachytes and pantellerites cogenetic with alkaline syenites, granites and rhyolitic flows and tuffs; Suite 2 (62 ± 2 Ma by K/Ar on basalt), a bimodal and complete series of alkali olivine basalts and associated microgabbro dykes, diorites, syenites and granites, cross-cutting the former. Kaersutite in the trachytes of Suite 1 has mantle-derived signatures: TiO2 > 4%, MgO < 15%, FeO > 8%, Ti = 0.63 c.p.f.u. and Al = 2, characteristic of kaersutites of HP and HT origin: 13-23 kbar, 1100-1220 °C. The trachytes are probably products of FC of a basaltic parent that did not attain higher crustal levels. The Suite 1 rocks are enriched in Rb, K, Zr, Nb, LREE, alkalis, and (Ce/Yb)N = 7-15 probably due to some effect of metasomatism during the magma ascension. Fe-Ti enrichment is corroborated by the presence of ferropseudobrookite-ilmenite-ulvospinel in the syenites and ilmenite in the pantellerite. The Rb/Ba > 1 in the trachytes (2.44, 26.7), pantellerite (6.33), alkaline granites (0.63-1.8) and the 87Sr/86Sr in the alkaline granites (=0.74060) depict the role of AFC. The ankaramites of the Suite 2 rocks are olivine-phyric (25%), Fo85-88, have 50-52% clinopyroxene (salite), 5% plagioclase (An55-36) and 7% Fe-Ti oxides. Trace element modeling indicates an origin from a basaltic magma of about 25% PM of spinel lherzolite mixed with a magma from <1% PM of garnet lherzolite (3-4% garnet) in a proportion of 1:4. The cogenetic alkali basalts and the microgabbro-diorite-syenite-granite that constitute the Suite 2 rocks, with a Daly gap of 54% > SiO2 < 58%, result from this Early Cenozoic magmatic event. The basalts have: Zr = 225-253, Nb = 98-111, Y = 33-56, typical of FOZO, a HIMU-type OIB related magmas (Sr/Sri = 0.70202-0.7034; Nd/Nd = 0.51282-0.512545; 206Pb/204Pb = 19.13, 207Pb/204Pb = 15

  20. Identification of an unradiogenic lead geochemical component below the East Pacific Rise (15°43'N)

    NASA Astrophysics Data System (ADS)

    Mougel, B.; Agranier, A.; Moreira, M. A.; Hemond, C.; Gente, P.

    2012-12-01

    Between the Rivera and Orozco Fracture Zones, the EPR is divided into 3 segments. One of them (the southern segment) is intersected around 15°43'N by a chain of seamounts that we will call the "mathematician seamounts". This segment is 300m shallower and twice wider than the rest of the EPR, which might suggest a bigger and localized magmatic supply in this part of the ridge. In this study, we explore the mantle source heterogeneities in this region, at a very small spatial-scale. We report major, trace element and isotope (Pb, Sr, Nd, Hf) compositions for 120 MORB samples, collected all along and across the ridge by submersible "Nautile" during cruise PaRiSub (2010). Trace elements patterns reveal that more enriched material than the source of typical N-MORB dominates the ambient upper mantle. They also exhibit an atypical pattern for some lava with depletion of LREE as well as HREE, and positive anomalies of Ba, Eu, and Sr. This observation is corroborated by isotopes. Isotopes compositions directly reflect the complex mixing processes affecting this restricted area. At least 3 distinct end-members have to be involved (2 significant principle components in the Pb isotope space). One of these components has novel geochemical properties, featuring the lowest 206Pb/204Pb and 208Pb/204Pb ratios of the whole EPR and even among all worldwide MORB while 207Pb/204Pb values remain relatively high. These extreme compositions are also associated with low 143Nd/144Nd and 176Hf/177Hf ratios, and high 86Sr/87Sr values, and therefore depict an unusual trend in all isotopic spaces. According to our observations and modeling, we suggest that these atypical MORB might be the first reported magmatic witnesses of the highly unradiogenic Pb mantle endmember depicted by Malaviarachchi et al (2008). Such material might be generated by the recycling of ancient lower crust, which was assimilated in the mantle as pyroxenitic/eclogitic veins before being partially melted. Trace elements

  1. Petrochemistry of igneous rocks of the California-Vetas mining district, Santander, Colombia: Implications for northern Andean tectonics and porphyry Cu (-Mo, Au) metallogeny

    NASA Astrophysics Data System (ADS)

    Bissig, Thomas; Mantilla Figueroa, Luis Carlos; Hart, Craig J. R.

    2014-07-01

    Porphyry Mo and Cu mineralization in the California-Vetas mining district is contemporaneous with 10.9 to 8.4 Ma granodiorite porphyry stocks and overprinted by Au-Ag mineralization of epithermal affinity. Mineralization is hosted by Grenvillian aged paragneisses (Bucaramanga Gneiss of the Santander Massif) and late Triassic to early Jurassic granitic rocks. All intrusive rocks are high-K calc-alkaline. Late Triassic to early Jurassic rocks include peraluminous granites with more than 70 wt.% SiO2 as well as metaluminous diorites, tonalites and granodiorites with SiO2 between 54.9 and 60.4 wt.%. Late Miocene rocks are weakly peraluminous granodiorite porphyries with SiO2 between 61 and 67 wt.% SiO2. Late Miocene rocks share some characteristics with adakite-like rocks which are widely associated with porphyry and epithermal style mineralization elsewhere in the Andes. They have high Ba (930 to 1500 ppm) and high Ba/La (28 to 50), high Sr (850 to 1100 ppm) and Sr/Y (48-78) and depleted middle rare earth elements (MREE) compared to the Mesozoic granites, which have 400 to 700 ppm Ba (Ba/La 14 to 25) and 80 to 150 ppm Sr (Sr/Y 2.5 to 14), and Mesozoic diorites and tonalites, which have ~ 900 to 1200 ppm Ba (Ba/La 20 to 32) and ~ 610 to 750 ppm Sr (Sr/Y 22 to 25). Miocene granodiorite porphyries, in contrast to Mesozoic intrusive rocks have only weak negative Eu anomalies. The Miocene rocks have 87Sr/86Sr ratios of 0.7052 to 0.7067 and εNd of - 1.9 to - 5.4 and are significantly more isotopically primitive than all other rocks in the study area including the Mesozoic diorites to tonalites (87Sr/86Sr = 0.7082 and 0.7092; εNd = - 6.7 and - 7.2), granites (87Sr/86Sr = 0.730 (n = 2); εNd = - 8.2 and - 8.3) and Bucaramanga Gneiss (0.718 to 0.743; εNd = - 10.8 to - 14.1). Lead isotope data are broadly consistent with the Sr and Nd isotope data and the Miocene porphyries have the lowest 207Pb/204Pb ratios but overlap with the Mesozoic diorites to tonalites in their 206Pb

  2. Geochemistry and petrogenesis of late Pleistocene to Recent volcanism in Southern Dominica, Lesser Antilles

    NASA Astrophysics Data System (ADS)

    Lindsay, J. M.; Trumbull, R. B.; Siebel, W.

    2005-12-01

    Dominica is the most productive volcanic island in the Lesser Antilles arc and contains the largest number of potentially active volcanoes, but is not well studied petrologically. Quaternary volcanic activity on Dominica has been dominated by intermediate to felsic magmas, erupted as large-volume ignimbrites (Roseau, Grand Savanne, Grand Bay) and dome complexes. One of the largest concentrations of these deposits, and one of the currently most active areas in terms of shallow seismicity and hotspring activity, is the Plat Pays Volcanic Complex (PPVC) at the southern tip of the island. The PPVC is made up of medium-K calc-alkaline silicic andesites and rarer dacites. The major and trace element compositions define regular variation trends that can be explained by fractionation of observed phenocryst phases (plagioclase, clinopyroxene, orthopyroxene, Fe-Ti oxides). The contemporary Morne Anglais center erupted a wider range of magmas, extending from silicic andesites (identical in composition to the PPVC) to basalt. The new geochemical and Sr-Nd-Pb isotope data presented here cover all main units of the PPVC and Morne Anglais, and give a reconnaisance view of three other important Quaternary volcanic centers on Dominica that are associated with large-volume ignimbrite eruptions: Diablotins, Wotten Waven/Micotrin and Trios Pitons. Geochemical modelling of variation trends from the PPVC and Anglais centers indicates these are consistent with derivation from a basaltic parent magma like that of Morne Anglais. With a few exceptions at the mafic end of the spectrum, Sr, Nd and Pb isotope ratios remain constant with fractionation from 52 to 64 wt.% SiO 2. The ɛNd values range from + 2 and + 4, and 87Sr / 86Sr between 0.7041 and 0.7047. The range of values for 208Pb / 204Pb, 207Pb / 204Pb and 206Pb / 204Pb are 39.2-39.4, 15.71-15.75, and 19.4-19.5, respectively. Exceptions to this are basalt scoria clasts from Anglais and an andesite dike cutting PPVC domes. These samples

  3. Stratigraphy, geochemistry and tectonic significance of the Oligocene magmatic rocks of western Oaxaca, southern Mexico

    USGS Publications Warehouse

    Martiny, B.; Martinez-Serrano, R. G.; Moran-Zenteno, D. J.; MacIas-Romo, C.; Ayuso, R.A.

    2000-01-01

    the volcanic rocks, from 0.7042 to 0.7046 and 0 +2.6. The range of these isotope ratios and those reported for the basement rocks in this region suggest a relatively low degree of old crustal involvement for most of the studied rocks. The Pb isotopic compositions of the Tertiary magmatic rocks also show a narrow range [(206Pb/204Pb) = 18.67-18.75; (207Pb/204Pb) = 15.59-15.62; (208Pb/204Pb) = 38.44-38.59], suggesting a similar source region for the volcanic and plutonic rocks. Trace elements and isotopic compositions suggest a mantle source in the subcontinental lithosphere that has been enriched by a subduction component. General tectonic features in this region indicate a more active rate of transtensional deformation for the inland volcanic region than along the coastal margin during the main events of Oligocene magmatism. The lower degree of differentiation of the inland volcanic sequences, particularly the upper unit of the northern sector, compared to the plutons of the coastal margin, suggests that the differentiation of the Tertiary magmas in southern Mexico was controlled to a great extent by the characteristics of the different strain domains. (C) 2000 Elsevier Science B.V. All rights reserved.

  4. Petrogenesis of Tertiary continental intra-plate lavas between Siebengebirge and Westerwald, Germany: Constraints from trace element systematics and Nd, Sr and Pb isotopes

    NASA Astrophysics Data System (ADS)

    Schubert, S.; Jung, S.; Pfänder, J. A.; Hauff, F.; Garbe-Schönberg, D.

    2015-10-01

    New 39Ar/40Ar ages and major- and trace-element and radiogenic isotope data are presented for basanites and alkali basalts from the transition area between the Westerwald and Siebengebirge volcanic fields (Germany) that belongs to the Central European Volcanic Province (CEVP). The 39Ar/40Ar ages indicate ages of c. 24 and c. 5 Ma which are fully compatible with previous K/Ar ages indicating that the evolution of this volcanic field belongs to the Westerwald area (28-22 Ma and 5 Ma) rather than to the Siebengebirge area (26-23 Ma). Based on the occurrence of > 30 isolated volcanic plugs with a simple igneous history, this volcanic field can be viewed as a monogenetic volcanic field. Compositions of some basanites are primitive, whereas others and the alkali basalts show decreasing Cr and Ni contents and CaO/Al2O3 ratios. However, increasing TiO2, Al2O3 and incompatible elements (Sr, Zr, Y, Hf, Ta) concentrations with decreasing MgO indicating fractionation of mainly olivine with minor amounts of clinopyroxene and spinel can be noticed. Rare earth element systematics suggest that most of the alkaline rocks are generated by different degrees of melting (5%-10%) of a garnet-bearing peridotite containing some residual amphibole. Negative anomalies of Rb and K in primitive mantle-normalized diagrams and a lack of Ba/Rb fractionation suggest that amphibole was the major OH-bearing mineral phase in the mantle. The alkaline rocks have a restricted range in 87Sr/86Sr and 143Nd/144Nd ratios ranging from 0.7033 to 0.7044 and from 0.51275 to 0.51285, respectively. Lead isotope compositions (206Pb/204Pb: 19.21-19.65; 207Pb/204Pb: 15.62-15.67; 208Pb/204Pb: 39.10-39.46) of the alkaline rocks are within the range of most OIB in which the higher values approach the composition of the European Asthenospheric Reservoir (EAR). The correlation between Sr and Nd isotopes and trace element constraints (Ce/Pb; Nb/U) indicates that for some samples interaction with crustal rocks during

  5. Stratigraphy, geochemistry and tectonic significance of the Oligocene magmatic rocks of western Oaxaca, southern Mexico

    NASA Astrophysics Data System (ADS)

    Martiny, Barbara; Martínez-Serrano, Raymundo G.; Morán-Zenteno, Dante J.; Macías-Romo, Consuelo; Ayuso, Robert A.

    2000-03-01

    volcanic rocks, from 0.7042 to 0.7046 and 0 to +2.6. The range of these isotope ratios and those reported for the basement rocks in this region suggest a relatively low degree of old crustal involvement for most of the studied rocks. The Pb isotopic compositions of the Tertiary magmatic rocks also show a narrow range [( 206Pb/ 204Pb)=18.67-18.75; ( 207Pb/ 204Pb)=15.59-15.62; ( 208Pb/ 204Pb)=38.44-38.59], suggesting a similar source region for the volcanic and plutonic rocks. Trace elements and isotopic compositions suggest a mantle source in the subcontinental lithosphere that has been enriched by a subduction component. General tectonic features in this region indicate a more active rate of transtensional deformation for the inland volcanic region than along the coastal margin during the main events of Oligocene magmatism. The lower degree of differentiation of the inland volcanic sequences, particularly the upper unit of the northern sector, compared to the plutons of the coastal margin, suggests that the differentiation of the Tertiary magmas in southern Mexico was controlled to a great extent by the characteristics of the different strain domains.

  6. Trace Element Signatures of Particles in the Fraser River Estuary

    NASA Astrophysics Data System (ADS)

    Snauffer, A. M.; Menard, O.; Kieffer, B.; Francois, R. H.; Weis, D. A.; Pcigr

    2010-12-01

    intermediate isotopic compositions may reflect a greater transport of particles from the headwaters (Proterozoic crust composition) to the mouth of the river (juvenile igneous rock composition). Future sampling during low flow conditions will determine signature sensitivities to flow variations. Measured ratios for Pb were 208Pb/204Pb = 38.014 to 38.378, 207Pb/204Pb = 15.620 to 15.651, and 206Pb/204Pb = 18.142 to 18.571 in the river and 37.551, 15.585, and 17.839 in the open straight respectively. An interesting observation is that Pb isotopic compositions fall on a mixing line between local anthropogenic end-members and natural sources. This trend is comparable to that of local highway soils and reflects the dominance of anthropogenic Pb in the metropolitan area. Further leaching experiments will be conducted to characterize the nature of this Pb signature. [1] Cameron and Hattori (1997) Chem Geol 137, 243-253 [2] Carpentier et al. (2010) Goldschmidt Conference [3] Cui and Russel (1995) GSAB, 107:127-138 [4] Preciado et al. (2007) Water Air Soil Pollut, DOI 10.1007/s11270-007-9402-4

  7. Archean Pb Isotope Evolution: Implications for the Early Earth.

    NASA Astrophysics Data System (ADS)

    Vervoort, J. D.; Thorpe, R.; Albarede, F.; Blichert-Toft, J.

    2008-12-01

    .728 Ga (Normetal) to 2.70 Ga (Noranda). The Pb isotopic compositions from these galenas, when normalized to a common age of 2.7 Ga, define a highly linear array in 207Pb/204Pb vs. 206Pb/204Pb. This array is nearly coincident with the 2.7 Ga geochron with a slope that corresponds to an age of ~4.4 Ga and with an extraordinary large range of 207Pb/204Pb, about the same magnitude as modern MORB. These data have important implications for the evolution of the Archean mantle. First, the slope of the Abitibi Pb-Pb array and its coincidence with the 2.7 Ga geochron suggests widespread U-Pb differentiation within the first hundred million years of Earth's history. This may have been due to either core formation or silicate/melt differentiation due to widespread melting of the mantle (e.g., formation of a magma ocean). Second, variations in μ in the Abitibi mantle and the subsequent Pb isotopic heterogeneities, whatever their cause, have not been significantly changed from 4.4 until 2.7 Ga. This implies that changes in μ in the Abitibi mantle source between 4.4 and 2.7 Ga, such as would be caused by crust extraction or recycling of older crust into this region of the mantle, were insufficient to destroy the original μ variations created at 4.4 Ga. Therefore, it appears that this portion of the mantle had essentially remained isolated and undisturbed from the early Hadean until the late Archean.

  8. Genesis of the Touissit-Bou Beker Mississippi valley-type district (Morocco-Algeria) and its relationship to the Africa-Europe collision

    USGS Publications Warehouse

    Bouabdellah, M.; Sangster, D.F.; Leach, D.L.; Brown, A.C.; Johnson, C.A.; Emsbo, P.

    2012-01-01

    isotope ratios ( 206Pb/ 204Pb = 18.319-18.390; 207Pb/ 204Pb = 15.620. 15.680; 208Pb/ 204Pb = 38.452-38.650) of sulfides are consistent with Pb being derived from the Visean rhyodacite and associated volcaniclastic rocks. The intimate link between faults and mineralization suggests the strong possibility of brine flow along both ENE-trending regional-scale faults and NW-SW-trending local-scale faults. The data suggest that MVT mineralization was emplaced during the late Neogene-Quaternary (i.e., ca. 15.0 Ma), possibly as a result of subsurface gravity-driven fluid flow in response to the collision between the African and Eurasian plates. ?? 2012 Society of Economic Geologists, Inc.

  9. Genesis of the Touissit-Bou Beker Mississippi Valley-type district (Morocco-Algeria) and its relation to the Africa-Europe collision

    USGS Publications Warehouse

    Bouabdellah, Mohammed; Sangster, Donald F.; Leach, David L.; Brown, Alex C.; Johnson, Craig A.; Emsbo, Poul

    2012-01-01

    isotope ratios (206Pb/204Pb = 18.319–18.390; 207Pb/204Pb = 15.620–15.680; 208Pb/204Pb = 38.452–38.650) of sulfides are consistent with Pb being derived from the Visean rhyodacite and associated volcaniclastic rocks. The intimate link between faults and mineralization suggests the strong possibility of brine flow along both ENE-trending regional-scale faults and NW-SW-trending local-scale faults. The data suggest that MVT mineralization was emplaced during the late Neogene-Quaternary (i.e., ca. 15–0 Ma), possibly as a result of subsurface gravity-driven fluid flow in response to the collision between the African and Eurasian plates.

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

    NASA Astrophysics Data System (ADS)

    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.

  11. Ore genesis of the Weibao lead-zinc district, Eastern Kunlun Orogen, China: constrains from ore geology, fluid inclusion and isotope geochemistry

    NASA Astrophysics Data System (ADS)

    Fang, Jing; Chen, Huayong; Zhang, Li; Zheng, Yi; Li, Dengfeng; Wang, Chengming; Shen, Dengliang

    2015-07-01

    samples from the Weibao lead-zinc district range between 18.259 and 18.336 for 206Pb/204Pb, 15.580 and 15.659 for 207Pb/204Pb, and 38.007 and 38.253 for 208Pb/204Pb, respectively, and the corresponding sulfur isotopic values range between -2.2 and 3.6 ‰. The fluid inclusion and isotope studies on the two deposits in the Weibao lead-zinc district suggest that they both have magmatic origin but mineralized by different mechanisms. Mineralization at the East Weibao deposit may be caused by fluid immiscibility and mixing, while at the West Weibao deposit, mineralization may result from water-rock reactions between magmatic fluid and impure carbonate wall rocks. Combined with geological observation, we conclude that the Weibao lead-zinc district as a united magmatic hydrothermal fluid system associated with the Triassic magmatism that widely distributes in the Qimantagh area.

  12. Origin of the granites and related Sn and Pb-Zn polymetallic ore deposits in the Pengshan district, Jiangxi Province, South China: constraints from geochronology, geochemistry, mineral chemistry, and Sr-Nd-Hf-Pb-S isotopes

    NASA Astrophysics Data System (ADS)

    Xu, Bin; Jiang, Shao-Yong; Luo, Lan; Zhao, Kui-Dong; Ma, Liang

    2016-05-01

    relatively higher δ34S values of 22.7-28.7 ‰. Lead isotopes indicate that the granites have higher 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios than the host Precambrian metasedimentary rocks, and the sulfide minerals from the orebodies fall in between them. Again, there is no difference for Pb isotopes between the Sn deposits (Huangjinwa, Zengjialong, Jianfengpo) and the Zhangshiba Pb-Zn deposit. The coincidence in S and Pb isotope compositions for Sn and Pb-Zn deposits suggests that similar sources for these mineralization, possibly derived from a mixed source of the granitic magmas and the Precambrian metasedimentary rocks. These data therefore favor of a magmatic-hydrothermal origin for both the Sn and Pb-Zn polymetallic mineralization in the Pengshan district.

  13. The role of slab melting in the petrogenesis of high-Mg andesites: evidence from Simbo Volcano, Solomon Islands

    NASA Astrophysics Data System (ADS)

    König, S.; Schuth, S.; Münker, C.; Qopoto, C.

    2007-01-01

    .4 to +7.9 and +12 to +14.4, respectively. These values reveal the presence of the Indian-Australian mantle domain beneath Simbo (i.e. the Indian-Australian plate) and also beneath all other volcanic islands of the New Georgia group, which are located north of the San Cristobál trench. 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values (18.43-18.52, 15.49-15.55 and 18.13-18.34, respectively) confirm the presence of slab melts from the subducted Pacific plate beneath southern Simbo where the highest Gd(N)/Yb(N) ratios are reported. A spatial shift towards an Indian-Australian slab signature is observed when approaching the active San Cristobál trench on northern Simbo, reflecting the decreasing influence of slab melts from the old subducted Pacific plate.

  14. Source and impact of lead contamination on δ-aminolevulinic acid dehydratase activity in several marine bivalve species along the Gulf of Cadiz.

    PubMed

    Company, R; Serafim, A; Lopes, B; Cravo, A; Kalman, J; Riba, I; DelValls, T A; Blasco, J; Delgado, J; Sarmiento, A M; Nieto, J M; Shepherd, T J; Nowell, G; Bebianno, M J

    2011-01-17

    Coastal areas and estuaries are particularly sensitive to metal contamination from anthropogenic sources and in the last few decades the study of space-time distribution and variation of metals has been extensively researched. The Gulf of Cadiz is no exception, with several rivers draining one of the largest concentrations of sulphide deposits in the world, the Iberian Pyrite Belt (IPB). Of these rivers, the Guadiana, one of the most important in the Iberian Peninsula, together with smaller rivers like the Tinto and Odiel, delivers a very high metal load to the adjacent coastal areas. The purpose of this work was to study the source and impact of lead (Pb) drained from historical or active mining areas in the IPB on the activity of a Pb inhibited enzyme (δ-aminolevulinic acid dehydratase, ALAD) in several bivalve species along the Gulf of Cadiz. Seven marine species (Chamelea gallina, Mactra corallina, Donax trunculus, Cerastoderma edule, Mytilus galloprovincialis, Scrobicularia plana and Crassostrea angulata) were collected at 12 sites from Mazagón, near the mouth of the rivers Tinto and Odiel (Spain), to Cacela Velha (Ria Formosa lagoon system, Portugal). Lead concentrations, ALAD activity and lead isotope ratios ((206)Pb/(204)Pb, (207)Pb/(204)Pb and (208)Pb/(204)Pb) were determined in the whole soft tissues. The highest Pb concentrations were determined in S. plana (3.50±1.09 μg g(-1) Pb d.w.) and D. trunculus (1.95±0.10 μg g(-1) Pb d.w.), while M. galloprovincialis and C. angulata showed the lowest Pb levels (<0.38 μg g(-1) Pb d.w.). In general, ALAD activity is negatively correlated with total Pb concentration. However this relationship is species dependent (e.g. linear for C. gallina ALAD=-0.36[Pb]+0.79; r=0.837; or exponential for M. galloprovincialis ALAD=2.48e(-8.3[Pb]); r=0.911). This indicates that ALAD activity has considerable potential as a biomarker of Pb and moreover, in marine bivalve species with different feeding habits. Lead isotope data

  15. Geodynamic control on melt production in the central Azores : new insights from major and trace elements, Sr, Nd, Pb, Hf isotopic data and K/Ar ages on the islands of Terceira, Sao Jorge and Faial

    NASA Astrophysics Data System (ADS)

    Hildenbrand, A.; Weis, D. A.; Madureira, P.; Marques, F. O.

    2012-12-01

    A combined geochronological and geochemical study has been carried out on the volcanic islands of Terceira, São Jorge, and Faial (central Azores) to examine the relationships between mantle dynamics, melt production and regional deformation close to the triple junction between the American, the Eurasian and the Nubian lithospheric plates. The lavas analyzed span the last 1.3 Myr, and have been erupted during two main periods prior to 800 ka and after 750 ka, respectively. They range in composition from alkaline basalts/basanites to trachytes, and overall exhibit a strong enrichment in highly incompatible elements. The whole range of isotopic compositions here reported (87Sr/86Sr: 0.703508-0.703913; 143Nd/144Nd: 0.512882-0.513010; 206Pb/204Pb: 19.0840- 20.0932; 207Pb/204Pb: 15.5388-15.6409; 208Pb/204Pb: 38.7416-39.3921; 176Hf/177Hf: 0.282956-0.283111) suggests the involvement of three components: (1) a weakly radiogenic component reflecting the source of regional MORBs, (2) a main HIMU-type component represented in the three islands, and (3) an additional component in Faial recent lavas, which appears similar to the EM type end-member previously recognized on other Azores eruptive complexes. The geographical distribution of the enriched components and the synchronous construction of various islands at the regional scale rules out a single narrow active plume. They suggest in turn the presence of dispersed residual enriched mantle blobs, interpreted as remnants from a large heterogeneous plume probably responsible for edification of the Azores plateau several Myr ago. The lavas erupted in São Jorge and Faial prior to 800 ka have similar and homogeneous isotopic ratios, which partly overlap the compositional field of MORBs from the adjacent portion of the Mid-Atlantic Ridge (MAR). Their genesis can be explained by the regional development of N150 transtensive tectonic structures, which promoted significant decompression melting of the upper mantle, with correlative

  16. Early-Cretaceous highly fractionated I-type granites from the northern Tengchong block, western Yunnan, SW China: Petrogenesis and tectonic implications

    NASA Astrophysics Data System (ADS)

    Zhu, Ren-Zhi; Lai, Shao-Cong; Qin, Jiang-Feng; Zhao, Shao-Wei

    2015-03-01

    Western Yunnan, an important constituent of the southeastern segment of the East Tethyan tectonic domain, lies along a transformed orientation from the NWW trending Himalayan-Tethyan segment to the northerly trending Southeast Asian segment. However, the geodynamical setting of the Early Cretaceous tectonothermal magmatism along the Bangong-Nujiang-Lushui-Luxi-Ruili belt as the Tethyan branch in western Yunnan (SW China) remains controversial. The Donghe granitoid, which is located between the Gaoligong and Tengliang belts in the northern Tengchong block, reveals its petrogenesis and its tectonics, both of which play a vital role in resolving previous disputes. Our zircon laser ablation inductively coupled plasma mass spectrometry U-Pb dating of granites from the Donghe batholith yields ages of 119.9 ± 0.9-130.6 ± 2.5 Ma. These granites display features typical of highly fractionated I-type granites: high SiO2 contents (>71 wt.%), high K contents (K2O = 3.88-5.66 wt.%), calc-alkaline character, slight peraluminosity (A/CNK = 1.02-1.16), and a highly differentiated index ranging from 83.6 to 95.6. In addition, as SiO2 contents increase, the rare earth element (REE) abundances, especially heavy REE abundances, and REE pattern slopes change gradually, but the negative Eu anomalies increase sharply, while the degree of enrichment in Rb, Th, U, and Pb and depletion in Ba, Nb, Sr, P, and Ti are enhanced. These features indicate that K-feldspar, ±plagioclase, ±biotite, ±amphibole, ±apatite, ±sphene/garnet, and ±Fe-Ti oxides such as ilmenite play the major role in the fractional crystallization process. The high initial 87Sr/86Sr (0.7067 and 0.7079) and negative εNd(t) values (-8.6 to -10.1), with T2DM ranging from 1.39 to 1.49 Ga, indicate that the sources were mainly derived from the mature ancient middle to lower crust and minor mantle-derived materials. The initial 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios of 18.462-18.646, 15.717-15.735, and 38

  17. Geochemistry and argon thermochronology of the Variscan Sila Batholith, southern Italy: source rocks and magma evolution

    USGS Publications Warehouse

    Ayuso, R.A.; Messina, A.; de Vivo, B.; Russo, S.; Woodruff, L.G.; Sutter, J.F.; Belkin, H.E.

    1994-01-01

    The Sila batholith is the largest granitic massif in the Calabria-Peloritan Arc of southern Italy, consisting of syn to post-tectonic, calc-alkaline and metaluminous tonalite to granodiorite, and post-tectonic, peraluminous and strongly peraluminous, two-mica??cordierite??Al silicate granodiorite to leucomonzogranite. Mineral 40Ar/39Ar thermochronologic analyses document Variscan emplacement and cooling of the intrusives (293-289 Ma). SiO2 content in the granitic rocks ranges from ???57 to 77 wt%; cumulate gabbro enclaves have SiO2 as low as 42%. Variations in absolute abundances and ratios involving Hf, Ta, Th, Rb, and the REE, among others, identify genetically linked groups of granitic rocks in the batholith: (1) syn-tectonic biotite??amphibole-bearing tonalites to granodiorites, (2) post-tectonic two-mica??Al-silicate-bearing granodiorites to leucomonzogranites, and (3) post-tectonic biotite??hornblende tonalites to granodiorites. Chondrite-normalized REE patterns display variable values of Ce/Yb (up to ???300) and generally small negative Eu anomalies. Degree of REE fractionation depends on whether the intrusives are syn- or post-tectonic, and on their mineralogy. High and variable values of Rb/Y (0.40-4.5), Th/Sm (0.1-3.6), Th/Ta (0-70), Ba/Nb (1-150), and Ba/Ta (???50-2100), as well as low values of Nb/U (???2-28) and La/Th (???1-10) are consistent with a predominant and heterogeneous crustal contribution to the batholith. Whole rock ??18O ranges from ???+8.2 to +11.7???; the mafic cumulate enclaves have the lowest ??18O values and the two-mica granites have the highest values. ??18O values for biotite??honblende tonalitic and granodioritic rocks (9.1 to 10.8???) overlap the values of the mafic enclaves and two-mica granodiorites and leucogranites (10.7 to 11.7???). The initial Pb isotopic range of the granitic rocks (206Pb/204Pb ???18.17-18.45, 207Pb/204Pb ???15.58-15.77, 208Pb/204Pb ???38.20-38.76) also indicates the predominance of a crustal source

  18. Geochemical and isotopic (Nd-Pb-Sr-O) variations bearing on the genesis of volcanic rocks from Vesuvius, Italy

    USGS Publications Warehouse

    Ayuso, R.A.; de Vivo, B.; Rolandi, G.; Seal, R.R.; Paone, A.

    1998-01-01

    commonly seen in rocks generated at orogenic margins are absent in our samples. Sr isotopic compositions are known to be variable within some of the units, in agreement with our data (87Sr/86Sr ~ 0.70699 to 0.70803) and with contributions from several isotopic components. Isotopic compositions for ??18O (7.3 to 10.2%), Pb for mineral separates and whole rocks (206Pb/204Pb ~ 18.947 to 19.178, 207Pb/204/Pb ~ 15.617 to 15.769, 208Pb/204Pb ~38.915 to 39.345), and Nd (143Nd ~ 0.51228 to 0.51251) also show variability. Oxygen isotope data show that pumices have higher ??18O values than cogenetic lavas, and that ??18O values and SiO2 are correlated. Radiogenic and stable isotope data plot within range of isotopic compositions for the Roman comagmatic province. Fractional crystallization cannot account for the radiogenic isotopic compositions of the Vesuvius magmas. We favor instead the combined effects of heterogeneous magma sources, together with isotopic exchange near the roof of the magma chamber. We suggest that metasomatized continental mantle lithosphere is the principal source of the magmas. This kind of enriched mantle was melted and reactivated in an area of continental extension (incipient rift setting) without direct reliance on contemporaneous subduction processes but possibly with input from mantle sources that resemble those that produce ocean island basalts.

  19. Tracing of ca 800 yr old mining activity in peat bog using Pb elemental concentrations and isotope compositions.

    NASA Astrophysics Data System (ADS)

    Baron, S.; Carignan, J.; Ploquin, A.

    2003-04-01

    Sixty sites of slags have been documented on the Mont-Lozère in southern France. The petrographic analysis shows that slags are metallurgical wastes (800 to 850 yr BP) which certainly result from smelting activity for lead and silver extraction (Ploquin et al., 2001). The aims of this study are: 1) to trace the source of Pb ores which supplied the smelting sites, by using the Pb isotopic composition of several surrounding Pb deposits, 2) to evaluate the actual pollution caused by these slags, by using elemental and isotopic compositions of soils, water and vegetation, and 3) to document the pollution history of the region, by using elemental and isotopic compositions of peat bog cores collected in the neighbourhood of the historical smelting sites. The lead isotopic composition of galena collected in most surrounding ores is very similar to that of different slag samples. On the other hand, the high precision of the results allowed us to select the mineralised areas which were probably the ore sources. The Pb isotopic composition of slags is even more homogeneous: 208/206 Pb: 2.092±0.002; 206/207 Pb: 1.179±0.001; 208/204 Pb: 38.663±0.025; 207/204 Pb: 15.665±0.006; 206/204 Pb: 18.476±0.023, and will allow source tracing in the environment. The "Narses Mortes" peat bog, around which two smelting sites have been reported, is strongly minerotrophic and contains 8 to 60% ash. A 1.40 m core have been retrieved and divided into 58 individual samples. Minerotrophic peat bog records both atmospheric deposition, soils leaching and the grounwater influence. The measured metal concentrations are normalised to Al contents of peat bog samples and the metal/Al ratios are compared to that of the Mont-Lozère granite: relative excess in metal concentrations are found in peat bog samples. An increasing excess of most metals (Pb, Zn, Cd...) was measured for surface samples, from 55 cm depth to the top of the core (23 cm depth). This profil might be attributed to atmospheric

  20. Zircon U-Pb and molybdenite Re-Os geochronology and Sr-Nd-Pb-Hf isotopic constraints on the genesis of the Xuejiping porphyry copper deposit in Zhongdian, Northwest Yunnan, China

    NASA Astrophysics Data System (ADS)

    Leng, Cheng-Biao; Zhang, Xing-Chun; Hu, Rui-Zhong; Wang, Shou-Xu; Zhong, Hong; Wang, Wai-Quan; Bi, Xian-Wu

    2012-10-01

    The Xuejiping porphyry copper deposit is located in northwestern Yunnan Province, China. Tectonically, it lies in the southern part of the Triassic Yidun island arc. The copper mineralization is mainly hosted in quartz-dioritic and quartz-monzonitic porphyries which intruded into clastic-volcanic rocks of the Late Triassic Tumugou Formation. There are several alteration zones including potassic, strong silicific and phyllic, argillic, and propylitic alteration zones from inner to outer of the mineralized porphyry bodies. The ages of ore-bearing quartz-monzonitic porphyry and its host andesite are obtained by using the zircon SIMS U-Pb dating method, with results of 218.3 ± 1.6 Ma (MSWD = 0.31, N = 15) and 218.5 ± 1.6 Ma (MSWD = 0.91, N = 16), respectively. Meanwhile, the molybdenite Re-Os dating yields a Re-Os isochronal age of 221.4 ± 2.3 Ma (MSWD = 0.54, N = 5) and a weighted mean age of 219.9 ± 0.7 Ma (MSWD = 0.88). They are quite in accordance with the zircon U-Pb ages within errors. Furthermore, all of them are contemporary with the timing of the Garzê-Litang oceanic crust subduction in the Yidun arc. Therefore, the Xuejiping deposit could be formed in a continental margin setting. There are negative ɛNd(t) values ranging from -3.8 to -2.1 and relatively high initial 87Sr/86Sr ratios from 0.7051 to 0.7059 for the Xuejiping porphyries and host andesites. The (206Pb/204Pb)t, (207Pb/204Pb)t and (208Pb/204Pb)t values of the Xuejiping porphyries and host andesites vary from 17.899 to 18.654, from 15.529 to 15.626, and from 37.864 to 38.52, respectively, indicative of high radiogenic Pb isotopic features. In situ Hf isotopic analyses on zircons by using LA-MC-ICP-MS exhibit that there are quite uniform and slightly positive ɛHf(t) values ranging from -0.2 to +3.2 (mostly between 0 and +2), corresponding to relatively young single-stage Hf model ages from 735 Ma to 871 Ma. These isotopic features suggest that the primary magmas of the Xuejiping porphyries and

  1. Fluid inclusions and isotopic characteristics of the Jiawula Pb-Zn-Ag deposit, Inner Mongolia, China

    NASA Astrophysics Data System (ADS)

    Li, Tiegang; Wu, Guang; Liu, Jun; Hu, Yanqing; Zhang, Yunfu; Luo, Dafeng; Mao, Zhihao

    2015-05-01

    The large Jiawula Pb-Zn-Ag deposit is located in the Derbugan metallogenic belt of the northern Great Xing'an Range. The vein style orebodies of the deposit occur along NWW- to NNW-trending fault zones. The ore-forming process at the deposit can be divided into three stages: an early quartz-pyrite-pyrrhotite-chalcopyrite stage, a middle quartz-carbonate-pyrite-galena-sphalerite stage, and a late quartz-carbonate-pyrite stage. Sulfide Rb-Sr dating indicates that the Jiawula deposit formed at ca. 143-142 Ma. Four types of fluid inclusions have been distinguished in quartz veins including liquid-rich, gas-rich, H2O-CO2, and daughter mineral-bearing inclusions. The fluid inclusions of the early stage are mainly liquid-rich, gas-rich, and H2O-CO2 types, with a small number containing daughter minerals. Cumulatively, the types have homogenization temperatures, densities, and salinities of 304-438 °C, 0.35-1.37 g/cm3, and 0.8-44.6 wt.% NaCl eqv., respectively. Inclusions of the middle stage are mainly liquid-rich and gas-rich types, with a small amount of H2O-CO2 and daughter mineral-bearing types; their homogenization temperatures, densities, and salinities vary from 242 °C to 297 °C, 0.71 to 1.44 g/cm3, and 0.4 wt.% to 36.8 wt.% NaCl eqv., respectively. The late stage only comprises liquid-rich inclusions with homogenization temperatures, densities, and salinities of 181-238 °C, 0.81-0.90 g/cm3, and 0.2-1.9 wt.% NaCl eqv., respectively. The ore-forming fluids of the Jiawula deposit are generally characterized by moderate temperature and low salinity and density, and belong to an H2O-NaCl-CO2 ± CH4 system. The δ18Owater values calculated for ore-bearing quartz vary from -13.4‰ to -9.1‰, and the δDV-SMOW values from bulk extraction of fluid inclusion waters vary from -166‰ to -133‰, suggesting that the ore-forming fluids mainly consist of meteoric water with a small amount of magmatic water. The δ34SV-CDT values range from 1.2‰ to 8.4‰. The 206Pb/204Pb

  2. Geochemical Evidence of a Near Surface History for the Source Rocks of the Central Coast Mountains Batholith, British Columbia

    NASA Astrophysics Data System (ADS)

    Stremtan, C. C.; Wetmore, P. H.; Ducea, M. N.

    2009-04-01

    Major and trace elemental concentrations as well as Sr, Pb and O isotopic data, completed on 41 plutonic samples from the Coast Mountains Batholith (CMB) ranging in age from ~108 Ma to ~50 Ma indicate that the source regions for these rocks were relatively uniform and typical for island arcs around the Pacific. The studied rocks are mineralogically and chemically metaluminous to weakly peraluminous and are mainly calc-alkaline with a few samples (mostly from the eastern part of the Coastal Shear Zone (CSZ) and three samples from the western part) showing a high-K calc-alkaline feature. Trace elements, especially REE, suggest a mafic source, probably oceanic plateau or island arc in origin, buried to different depths in the crust and that underwent various degrees of partial melting. Initial whole-rock 87Sr/86Sr range from 0.7035 up to 0.7053, whereas lead isotopic data range from 18.586 to 19.078 for 206Pb/204Pb, 15.545 to 15.634 for 207Pb/204Pb, and 37.115 to 38.661 for 208Pb/204Pb. In contrast to these fairly primitive isotopic data, δ18O values for quartz separates determined for 19 of the samples range from 6.8 up to 10.0 . Such δ18O values exclude the possibility that these melts were solely generated from the Mesozoic mantle wedge of this continental arc, just as the Sr and Pb data preclude significant involvement of an old (Precambrian) crustal/mantle lithospheric source. We interpret the high δ18O component to represent materials that had a multi-stage crustal evolution. They were originally mafic rocks derived from a circum-Pacific juvenile mantle wedge that experienced a period of near surface residence after initial crystallization. During this interval these primitive rocks interacted with meteoric waters at low temperatures, as indicated by the high δ18O values. Subsequently, these materials were buried to lower crustal depths where they re-melted to form the high δ18O component of the CMB. We estimate that, based on REE ratios and the presence of

  3. Petrogenesis of basaltic volcanic rocks from the Pribilof Islands, Alaska, by melting of metasomatically enriched depleted lithosphere, crystallization differentiation, and magma mixing

    USGS Publications Warehouse

    Chang, J.M.; Feeley, T.C.; Deraps, M.R.

    2009-01-01

    The Pribilof Islands, Alaska, are located in the Bering Sea in a continental intraplate setting. In this study we examine the petrology and geochemistry of volcanic rocks from St. Paul (0??54-0??003 Ma) and St. George (2??8-1??4 Ma) Islands, the two largest Pribilof Islands. Rocks from St. George can be divided into three groups: group 1 is a high-MgO, low-SiO. 2 suite composed primarily of basanites; group 2 is a high-MgO, high-SiO 2 suite consisting predominantly of alkali basalts; group 3 is an intermediate- to low-MgO suite that includes plagioclase-phyric subalkali basalts and hawaiites. Major and trace element geochemistry suggests that groups 1 and 2 formed by small-degree partial melting of amphibole-bearing to amphibole-free garnet peridotite. Group 1 rocks were the earliest melts produced from the most hydrous parts of the mantle, as they show the strongest geochemical signature of amphibole in their source. The suite of rocks from St. Paul ranges from 14??4 to 4??2 wt % MgO at relatively constant SiO 2 contents (43??1-47??3 wt %). The most primitive St. Paul rocks are modeled as mixtures between magmas with compositions similar to groups 1 and 2 from St. George Island, which subsequently fractionated olivine, clinopyroxene, and spinel to form more evolved rocks. Plagioclase-phyric group 3 rocks from St. George are modeled as mixtures between an evolved melt similar to the evolved magmas on St. Paul and a fractionated group 2 end-member from St. George. Mantle potential temperatures estimated for primitive basanites and alkali basalts are ???1400??C and are similar to those of mid-ocean ridge basalts (MORB). Similarly, 87Sr/. 86Sr and 143Nd/. 144Nd values for all rocks are MORB-like, in the range of 0??702704-0??703035 and 0??513026-0??513109, respectively. 208Pb/. 204Pb vs 206Pb/. 204Pb values lie near the MORB end-member but show a linear trend towards HIMU (high time-integrated 238U/. 204Pb). Despite isotopic similarities to MORB, many of the major and

  4. Source and impact of lead contamination on δ-aminolevulinic acid dehydratase activity in several marine bivalve species along the Gulf of Cadiz.

    PubMed

    Company, R; Serafim, A; Lopes, B; Cravo, A; Kalman, J; Riba, I; DelValls, T A; Blasco, J; Delgado, J; Sarmiento, A M; Nieto, J M; Shepherd, T J; Nowell, G; Bebianno, M J

    2011-01-17

    Coastal areas and estuaries are particularly sensitive to metal contamination from anthropogenic sources and in the last few decades the study of space-time distribution and variation of metals has been extensively researched. The Gulf of Cadiz is no exception, with several rivers draining one of the largest concentrations of sulphide deposits in the world, the Iberian Pyrite Belt (IPB). Of these rivers, the Guadiana, one of the most important in the Iberian Peninsula, together with smaller rivers like the Tinto and Odiel, delivers a very high metal load to the adjacent coastal areas. The purpose of this work was to study the source and impact of lead (Pb) drained from historical or active mining areas in the IPB on the activity of a Pb inhibited enzyme (δ-aminolevulinic acid dehydratase, ALAD) in several bivalve species along the Gulf of Cadiz. Seven marine species (Chamelea gallina, Mactra corallina, Donax trunculus, Cerastoderma edule, Mytilus galloprovincialis, Scrobicularia plana and Crassostrea angulata) were collected at 12 sites from Mazagón, near the mouth of the rivers Tinto and Odiel (Spain), to Cacela Velha (Ria Formosa lagoon system, Portugal). Lead concentrations, ALAD activity and lead isotope ratios ((206)Pb/(204)Pb, (207)Pb/(204)Pb and (208)Pb/(204)Pb) were determined in the whole soft tissues. The highest Pb concentrations were determined in S. plana (3.50±1.09 μg g(-1) Pb d.w.) and D. trunculus (1.95±0.10 μg g(-1) Pb d.w.), while M. galloprovincialis and C. angulata showed the lowest Pb levels (<0.38 μg g(-1) Pb d.w.). In general, ALAD activity is negatively correlated with total Pb concentration. However this relationship is species dependent (e.g. linear for C. gallina ALAD=-0.36[Pb]+0.79; r=0.837; or exponential for M. galloprovincialis ALAD=2.48e(-8.3[Pb]); r=0.911). This indicates that ALAD activity has considerable potential as a biomarker of Pb and moreover, in marine bivalve species with different feeding habits. Lead isotope data

  5. The Amazon-Laurentian connection as viewed from the Middle Proterozoic rocks in the central Andes, western Bolivia and northern Chile

    USGS Publications Warehouse

    Tosdal, R.M.

    1996-01-01

    Middle Proterozoic rocks underlying the Andes in western Bolivia, western Argentina, and northern Chile and Early Proterozoic rocks of the Arequipa massif in southern Peru?? from the Arequipa-Antofalla craton. These rocks are discontinuously exposed beneath Mesozoic and Cenozoic rocks, but abundant crystalline clasts in Tertiary sedimentary rocks in the western altiplano allow indirect samples of the craton. Near Berenguela, western Bolivia, the Oligocene and Miocene Mauri Formation contains boulders of granodiorite augen gneiss (1171??20 Ma and 1158??12 Ma; U-Pb zircon), quartzose gneiss and granofels that are inferred to have arkosic protoliths (1100 Ma source region; U-Pb zircon), quartzofeldspathic and mafic orthogneisses that have amphibolite- and granulite-facies metamorphic mineral assemblages (???1080 Ma metamorphism; U-Pb zircon), and undeformed granitic rocks of Phanerozoic(?) age. The Middle Proterozoic crystalline rocks from Berenguela and elsewhere in western Bolivia and from the Middle Proterozoic Bele??n Schist in northern Chile generally have present-day low 206Pb/204Pb ( 15.57), and elevated 208Pb/204Pb (37.2 to 50.7) indicative of high time-averaged Th/U values. The Middle Proterozoic rocks in general have higher presentday 206Pb/204Pb values than those of the Early Proterozoic rocks of the Arequipa massif (206Pb/204Pb between 16.1 and 17.1) but lower than rocks of the southern Arequipa-Antofalla craton (206Pb/204Pb> 18.5), a difference inferred to reflect Grenvillian granulite metamorphism. The Pb isotopic compositions for the various Proterozoic rocks lie on common Pb isotopic growth curves, implying that Pb incorporated in rocks composing the Arequipa-Antofalla craton was extracted from a similar evolving Pb isotopic reservoir. Evidently, the craton has been a coherent terrane since the Middle Proterozoic. Moreover, the Pb isotopic compositions for the Arequipa-Antofalla craton overlap those of the Amazon craton, thereby supporting a link

  6. Pb-Sr-Nd isotopes in surficial materials at the Pebble Porphyry Cu-Au-Mo Deposit, Southwestern Alaska: can the mineralizing fingerprint be detected through cover?

    USGS Publications Warehouse

    Ayuso, Robert A.; Kelley, Karen D.; Eppinger, Robert G.; Forni, Francesca

    2013-01-01

    The Cretaceous Pebble porphyry Cu-Au-Mo deposit is covered by tundra and glacigenic sediments. Pb-Sr-Nd measurements were done on sediments and soils to establish baseline conditions prior to the onset of mining operations and contribute to the development of exploration methods for concealed base metal deposits of this type. Pebble rocks have a moderate range for 206Pb/204Pb = 18.574 to 18.874, 207Pb/204Pb = 15.484 to 15.526, and 208,Pb/204Pb = 38.053 to 38.266. Mineralized granodiorite shows a modest spread in 87Sr/86Sr (0.704354–0.707621) and 143Nd/144Nd (0.512639–0.512750). Age-corrected (89 Ma) values for the granodiorite yield relatively unradiogenic Pb (e.g., 207Pb/204Pb 87Sr/86Sr, and positive values of ɛNd (1.00–4.52) that attest to a major contribution of mantle-derived source rocks. Pond sediments and soils have similar Pb isotope signatures and 87Sr/86Sr and 143Nd/144Nd values that resemble the mineralized granodiorites. Glacial events have obscured the recognition of isotope signatures of mineralized rocks in the sediments and soils. Baseline radiogenic isotope compositions, prior to the onset of mining operations, reflect natural erosion, transport and deposition of heterogeneous till sheets that included debris from barren rocks, mineralized granodiorite and sulfides from the Pebble deposit, and other country rocks that pre- and postdate the mineralization events. Isotopic variations suggest that natural weathering of the deposit is generally reflected in these surficial materials. The isotope data provide geochemical constraints to glimpse through the extensive cover and together with other geochemical observations provide a vector to concealed mineralized rocks genetically linked with the Pebble deposit.

  7. Major Pb Loss in the Silicate Earth at ~ 4.52 Ga

    NASA Astrophysics Data System (ADS)

    Vervoort, J. D.; Albarede, F.; Blichert-Toft, J.; Thorpe, R.

    2009-12-01

    The Pb isotopic compositions of galenas from volcanogenic massive sulfide (VMS) deposits have been used widely in the past to track terrestrial Pb evolution for several important reasons. First, the galenas in the VMS ores have U/Pb=0, which lock in their Pb isotopic compsitions at the time of their formation. Second, the syngenetic nature of the VMS ores means that the galenas likely average the Pb isotopic composition of the host volcanic rocks. Third, many VMS deposits are hosted by juvenile mantle-derived rocks with little or no interaction with older evolved crust. In this study we focused on the VMS deposits in the Abitibi and Wawa greenstone belts (Subprovinces) in the Superior Province of Canada. All deposits are late Archean in age (~2.7 Ga) and are hosted by juvenile, mantle-derived volcanic rocks, as evidenced by both their Nd and Hf isotopic compositions. We analyzed the Pb isotopic compositions of galenas from 8 VMS districts in the Abitibi and Wawa greenstone belts. Each individual VMS district has a narrow range of Pb isotopic compositions but collectively the deposits define a coherent array with the least radiogenic compositions at Matagami (207Pb/204Pb = 14.32 and 206Pb/204Pb = 13.11) and the most radiogenic compositions at Noranda (207Pb/204Pb = 14.49 and 206Pb/204Pb = 13.31), both in the Abitibi greenstone belt. These districts differ in age by nearly 30 m.y. from 2.73 Ga to 2.70 Ga. When these compositions are normalized to a common age of 2.70 Ga, they define a highly linear array in 207Pb/204Pb and 206Pb/204Pb. Using single stage Pb evolution beginning at 4.56 the VMS array at 2.7 Ga lies to the right of the Geochron and aligns with the 2.62 Ga Geochron in future Pb space. This assumes, however, that Earth’s major U/Pb fractionation occurs at 4.56 Ga and that silicate Earth Pb evolves with a high μ throughout its history. A more likely scenario is that Pb began with a very low μ in the solar nebula, increased moderately due to volatile

  8. The Golden Ratio

    ERIC Educational Resources Information Center

    Hyde, Hartley

    2004-01-01

    The Golden Ratio is sometimes called the "Golden Section" or the "Divine Proportion", in which three points: A, B, and C, divide a line in this proportion if AC/AB = AB/BC. "Donald in Mathmagicland" includes a section about the Golden Ratio and the ratios within a five-pointed star or pentagram. This article presents two computing exercises that…

  9. Isotopic Constraints on Magmatic Sources at Nyiragongo and Nyamulagira Volcanoes, Virunga Volcanic Province, DR Congo

    NASA Astrophysics Data System (ADS)

    Phillips, E. H. W.; Sims, K. W. W.; Tedesco, D.; Blichert-Toft, J.; Scott, S. R.; Reagan, M. K.

    2015-12-01

    The active volcanoes Nyiragongo and Nyamulagira in the DR Congo have very different physical and geochemical characteristics, despite being situated a mere 15 km apart. Nyiragongo's foiditic lavas are some of the most silica-undersaturated on earth, whereas the highly effusive Nyamulagira erupts primarily basanites and tephrites. To determine the extent and scale of mantle heterogeneities and gain insight into the magmatic sources beneath this portion of the East African Rift, we have measured Hf and Pb isotope compositions for 43 samples from Nyiragongo and Nyamulagira. The Nd and Sr isotope data for the same sample dissolutions are forthcoming. Nyiragongo lavas are clearly distinct from Nyamulagira lavas in terms of their Hf and Pb isotope compositions, suggesting that a long-lived and small-scale heterogeneous mantle source exists beneath these two volcanoes. Nyiragongo lavas have ɛHf ranging from +1.8 to +5.5 with an average of +2.9 (n=29) and 206Pb/204Pb ranging from 19.4049 to 19.7252 with an average of 19.6329 (n=29). Nyamulagira lavas have ɛHf ranging from -0.5 to +1.5 with an average of +0.5 (n=14) and 206Pb/204Pb ranging from 19.2518 to 19.2828 with an average of 19.2663 (n=13). Nyiragongo lavas erupted in 2002 or later have amongst the highest 206Pb/204Pb within this suite of samples. We note that Chakrabarti et al. (2009, Chem Geol 259) measured bulk silicate earth-like Nd and Sr isotope compositions for Nyiragongo lavas and proposed a primitive mantle/bulk-earth plume source for this volcano. Our new Hf isotope compositions for Nyiragongo, however, are higher than bulk silicate earth, suggesting a more depleted source for these highly alkaline lavas. We also note that the He isotope compositions of olivine and clinopyroxene from Nyiragongo lavas (R/Ra = 6.7-8.5; Pik et al., 2006, Chem Geol 226; Tedesco et al., 2010, J Geophys Res 115) are inconsistent with a long-term bulk silicate earth-like source.

  10. Isotope geochemistry of early Kilauea magmas from the submarine Hilina bench: The nature of the Hilina mantle component

    USGS Publications Warehouse

    Kimura, Jun-Ichi; Sisson, Thomas W.; Nakano, Natsuko; Coombs, Michelle L.; Lipman, Peter W.

    2006-01-01

    Submarine lavas recovered from the Hilina bench region, offshore Kilauea, Hawaii Island provide information on ancient Kilauea volcano and the geochemical components of the Hawaiian hotspot. Alkalic lavas, including nephelinite, basanite, hawaiite, and alkali basalt, dominate the earliest stage of Kilauea magmatism. Transitional basalt pillow lavas are an intermediate phase, preceding development of the voluminous tholeiitic subaerial shield and submarine Puna Ridge. Most alkalic through transitional lavas are quite uniform in Sr–Nd–Pb isotopes, supporting the interpretation that variable extent partial melting of a relatively homogeneous source was responsible for much of the geochemical diversity of early Kilauea magmas (Sisson et al., 2002). These samples are among the highest 206Pb/204Pb known from Hawaii and may represent melts from a distinct geochemical and isotopic end-member involved in the generation of most Hawaiian tholeiites. This end-member is similar to the postulated literature Kea component, but we propose that it should be renamed Hilina, to avoid confusion with the geographically defined Kea-trend volcanoes. Isotopic compositions of some shield-stage Kilauea tholeiites overlap the Hilina end-member but most deviate far into the interior of the isotopic field defined by magmas from other Hawaiian volcanoes, reflecting the introduction of melt contributions from both “Koolau” (high 87Sr/86Sr, low 206Pb/204Pb) and depleted (low 87Sr/86Sr, intermediate 206Pb/204Pb) source materials. This shift in isotopic character from nearly uniform, end-member, and alkalic, to diverse and tholeiitic corresponds with the major increase in Kilauea's magmatic productivity. Two popular geodynamic models can account for these relations: (1) The upwelling mantle source could be concentrically zoned in both chemical/isotopic composition, and in speed/extent of upwelling, with Hilina (and Loihi) components situated in the weakly ascending margins and the

  11. Jurassic metabasic rocks in the Kızılırmak accretionary complex (Kargı region, Central Pontides, Northern Turkey)

    NASA Astrophysics Data System (ADS)

    Çelik, Ömer Faruk; Chiaradia, Massimo; Marzoli, Andrea; Özkan, Mutlu; Billor, Zeki; Topuz, Gültekin

    2016-03-01

    The Kızılırmak accretionary complex near Kargı is tectonically bounded by the Jurassic and Early Cretaceous metamorphic massives of the Central Pontides. It consists mainly of serpentinite, serpentinized peridotite, gabbro, basalt, metabasite and deep-marine sedimentary rocks. The metabasites in the Kızılırmak accretionary complex are tectonically located within a serpentinite, radiolarian chert, spilitized basalt, gabbro association and commonly display a steep contact with serpentinites. Amphiboles from metabasites yielded robust 40Ar/39Ar plateau ages ranging between 159.4 ± 0.4 Ma and 163.5 ± 0.8 Ma. These are interpreted as cooling ages of the metabasites. The metabasites have 87Sr/86Sr(i) between 0.7035 and 0.7044 and 206Pb/204Pb(i) ranging between 18.18 and 18.92. The gabbros have higher 87Sr/86Sr(i) between 0.7044 and 0.7060 and 206Pb/204Pb(i) ranging between 17.98 and 18.43. Three basalt samples display 87Sr/86Sr(i) between 0.7040 and 0.7059. Their 206Pb/204Pb(i) are unrealistically low (15.42 and 15.62), suggesting, most likely, Pb loss which results in over-corrected values for decay through time. Pb-Sr-Nd isotopic compositions for all samples consistently plot between the fields of MORB or the Depleted MORB Mantle reservoirs and enriched mantle reservoirs (EMII rather than EMI). All the samples (except one dolerite dike) have negative ɛNdDM(t = 160 Ma) values, suggesting derivation from a reservoir more enriched than the depleted mantle. The protoliths of metabasites correspond to diverse sources (N-MORB, E-MORB, OIB and IAT) based on whole rock major and trace element composition. An IAT-like protolith for the metabasites indicates that the İzmir-Ankara-Erzincan ocean domain was subducting and the tectonic regime was compressional during Late Jurassic and before. The protoliths of these rocks were metamorphosed during the subduction/accretion processes, as observed in the metamorphic rocks located along the Balkan, Northern Turkey and

  12. Isotopic and trace element compositions of upper mantle and lower crustal xenoliths, Cima volcanic field, California: Implications for evolution of the subcontinental lithospheric mantle

    USGS Publications Warehouse

    Mukasa, S.B.; Wilshire, H.G.

    1997-01-01

    Ultramafic and mafic xenoliths from the Cima volcanic field, southern California, provide evidence of episodic modification of the upper mantle and underplating of the crust beneath a portion of the southern Basin and Range province. The upper mantle xenoliths include spinel peridotite and anhydrous and hydrous pyroxenite, some cut by igneous-textured pyroxenite-gabbro veins and dikes and some by veins of amphibole ?? plagioclase. Igneous-textured pyroxenites and gabbros like the dike rocks also occur abundantly as isolated xenoliths inferred to represent underplated crust. Mineral and whole rock trace element compositions among and within the different groups of xenoliths are highly variable, reflecting multiple processes that include magma-mantle wall rock reactions, episodic intrusion and it filtration of basaltic melts of varied sources into the mantle wall rock, and fractionation. Nd, Sr, and Pb isotopic compositions mostly of clinopyroxene and plagioclase mineral separates show distinct differences between mantle xenoliths (??Nd = -5.7 to +3.4; 87Sr/86Sr = 0.7051 - 0.7073; 206Pb/204Pb = 19.045 - 19.195) and the igneous-textured xenoliths (??Nd = +7.7 to +11.7; 87Sr/86Sr = 0.7027 - 0.7036 with one carbonate-affected outlier at 0.7054; and 206Pb/204Pb = 18.751 - 19.068), so that they cannot be related. The igneous-textured pyroxenites and gabbros are similar in their isotopic compositions to the host basaltic rocks, which have ??Nd of+5.1 to +9.3; 87Sr/86Sr of 0.7028 - 0.7050, and 206Pb/204Pb of 18.685 - 21.050. The igneous-textured pyroxenites and gabbros are therefore inferred to be related to the host rocks as earlier cogenetic intrusions in the mantle and in the lower crust. Two samples of peridotite, one modally metasomatized by amphibole and the other by plagioclase, have isotopic compositions intermediate between the igneous-textured xenoliths and the mantle rock, suggesting mixing, but also derivation of the metasomatizing magmas from two separate and

  13. Subalkaline andesite from Valu Fa Ridge, a back-arc spreading center in southern Lau Basin: petrogenesis, comparative chemistry, and tectonic implications

    USGS Publications Warehouse

    Vallier, T.L.; Jenner, G.A.; Frey, F.A.; Gill, J.B.; Davis, A.S.; Volpe, A.M.; Hawkins, J.W.; Morris, J.D.; Cawood, Peter A.; Morton, J.L.; Scholl, D. W.; Rautenschlein, M.; White, W.M.; Williams, Ross W.; Stevenson, A.J.; White, L.D.

    1991-01-01

    Tholeiitic andesite was dredged from two sites on Valu Fa Ridge (VFR), a back-arc spreading center in Lau Basin. Valu Fa Ridge, at least 200 km long, is located 40-50 km west of the active Tofua Volcanic Arc (TVA) axis and lies about 150 km above the subducted oceanic plate. One or more magma chambers, traced discontinuously for about 100 km along the ridge axis, lie 3-4 km beneath the ridge. The mostly aphyric and glassy lavas had high volatile contents, as shown by the abundance and large sizes of vesicles. An extensive fractionation history is inferred from the high SiO2 contents and FeO* MgO ratios. Chemical data show that the VFR lavas have both volcanic arc and back-arc basin affinities. The volcanic arc characteristics are: (1) relatively high abundances of most alkali and alkaline earth elements; (2) low abundances of high field strength elements Nb and Ta; (3) high U/Th ratios; (4) similar radiogenic isotope ratios in VFR and TVA lavas, in particular the enrichment of 87Sr 86Sr relative to 206Pb 204Pb; (5) high 238U 230Th, 230Th 232Th, and 226Ra 230Th activity ratios; and (6) high ratios of Rb/Cs, Ba/Nb, and Ba/La. Other chemical characteristics suggest that the VFR lavas are related to MORB-type back-arc basin lavas. For example, VFR lavas have (1) lower 87Sr 86Sr ratios and higher 143Nd 144Nd ratios than most lavas from the TVA, except samples from Ata Island, and are similar to many Lau Basin lavas; (2) lower Sr/REE, Rb/Zr, and Ba/Zr ratios than in arc lavas; and (3) higher Ti, Fe, and V, and higher Ti/V ratios than arc lavas generally and TVA lavas specifically. Most characteristics of VFR lavas can be explained by mixing depleted mantle with either small amounts of sediment and fluids from the subducting slab and/or an older fragment of volcanic arc lithosphere. The eruption of subalkaline andesite with some arc affinities along a back-arc spreading ridge is not unique. Collision of the Louisville and Tonga ridges probably activated back-arc extension

  14. South Atlantic DUPAL anomaly — Dynamic and compositional evidence against a recent shallow origin

    NASA Astrophysics Data System (ADS)

    Class, Cornelia; le Roex, Anton

    2011-05-01

    The DUPAL anomaly in the South Atlantic is present in intra-plate volcanism associated with the Tristan-Gough, Discovery and Shona plumes, and along adjacent sections of the southern Mid-Atlantic Ridge, and has been variably attributed to either shallow continental or deep recycled sources. Based on geodynamic considerations, we identify the Namaqua-Natal Belt of southern Africa as the most likely origin of any subcontinental lithospheric mantle (SCLM) or lower continental crust (LCC) recently introduced into the source of DUPAL oceanic basalts by processes of plume erosion of the SCLM, general erosion of the SCLM by the mantle flow field, or tectonic detachment of SCLM and LCC related to continental breakup. Sr and Pb isotopic compositions of clinopyroxenes of SCLM xenoliths from the Proterozoic Namaqua-Natal Belt (Uintjiesberg, Markt, Hebron) are measured by laser MC-ICPMS. The inferred isotopic composition of the SCLM spans a large range with 206Pb/ 204Pb ~ 18.2 to 19.4, 208Pb/ 204Pb ~ 37.5 to 39.2 and 87Sr/ 86Sr ~ 0.704 to 0.716. In contrast, lower crustal samples from the Proterozoic Namaqua-Natal Belt (Uintjiesberg, Markt, Hebron, Cordaatskuil, and Lovedale) are unradiogenic in Pb isotopic composition (whole rock data) with 206Pb/ 204Pb ~ 14.2 to 18.5, 208Pb/ 204Pb ~ 34.5 to 37.8 and 87Sr/ 86Sr ~ 0.703 to 0.715. Sr-Nd-Pb isotopic compositions of samples from Vema and the 7°E seamounts constrain the upper mantle composition away from lower mantle plumes. None of the measured SCLM, LCC and seamount samples show DUPAL signatures. The new results, in combination with literature data, provide no evidence for an origin of the DUPAL signature from recent introduction of continental material as a shallow component in the source of DUPAL oceanic basalts. Rather, the distribution of a more diluted DUPAL signature in plume-influenced MORB along sections of the southern Mid-Atlantic Ridge spatially associated with intra-plate volcanism carrying the DUPAL signature

  15. Upper and lower crust recycling in the source of CAMP basaltic dykes from southeastern North America

    NASA Astrophysics Data System (ADS)

    Callegaro, Sara; Marzoli, Andrea; Bertrand, Hervé; Chiaradia, Massimo; Reisberg, Laurie; Meyzen, Christine; Bellieni, Giuliano; Weems, Robert E.; Merle, Renaud

    2013-08-01

    The densest dykes swarm of the Central Atlantic magmatic province (CAMP) occur in southeastern North America (SENA) and were intruded between 202 and 195 Ma during Pangea break-up. New combined geochemical data (major and trace elements, Sr-Nd-Pb-Os isotopes) constrain the mantle source of these magmatic bodies and their evolution path. While Sr-Nd isotopic compositions for SENA rocks (87Sr/86Sr200Ma 0.70438-0.70880 and 143Nd/144Nd200Ma 0.51251-0.51204) fall within the low-Ti CAMP field, Pb-Pb isotopes (206Pb/204Pb200Ma 17.46-18.85, 207Pb/204Pb200Ma 15.54-15.65, 208Pb/204Pb200Ma 37.47-38.76) are peculiar to this area of the CAMP and cover a considerable span of compositions, especially in 206Pb/204Pb200Ma. Given the generally unradiogenic Os isotopic compositions (187Os/188Os200Ma 0.127-0.144) observed and the lack of correlation between these and other geochemical markers, crustal contamination during the evolution of SENA dykes must have been limited (less than 10%). Thus the isotopic variation is interpreted to reside primarily within the mantle source. These observations, coupled with typical continental signatures in trace elements (positive anomaly in Pb and negative anomalies in Ti and Nb), require another means of conveying a continental flavor to these magmas, which is here hypothesized to be the shallow recycling within the upper mantle of subducted lower and upper crustal materials. Pseudo-ternary mixing models show that a maximum of 10% recycled crust is enough to explain their trace element patterns as well as their isotopic heterogeneity. Looking at the larger picture of the origin of the CAMP, the thermal contribution of a mantle plume cannot be ruled out due to the relatively high mantle potential temperatures (1430-1480 °C) calculated for high-Fo SENA olivines. Nevertheless, our results suggest that the chemical involvement of a mantle plume is negligible (less than 5%) if either a C- or an EM-flavored plume is considered. Rather, the possibility

  16. Major element, REE, and Pb, Nd and Sr isotopic geochemistry of Cenozoic volcanic rocks of eastern China: implications for their origin from suboceanic-type mantle reservoirs

    USGS Publications Warehouse

    Basu, A.R.; Wang, Junwen; Huang, Wankang; Xie, Guanghong; Tatsumoto, M.

    1991-01-01

    Major- and rare-earth-element (REE) concentrations and UThPb, SmNd, and RbSr isotope systematics are reported for Cenozoic volcanic rocks from northeastern and eastern China. These volcanic rocks, characteristically lacking the calc-alkaline suite of orogenic belts, were emplaced in a rift system which formed in response to the subduction of the western Pacific plate beneath the eastern Asiatic continental margin. The rocks sampled range from basanite and alkali olivine basalt, through olivine tholeiite and quartz tholeiite, to potassic basalts, alkali trachytes, pantellerite, and limburgite. These rock suites represent the volcanic centers of Datong, Hanobar, Kuandian, Changbaishan and Wudalianchi in northeastern China, and Mingxi in the Fujian Province of eastern China. The major-element and REE geochemistry is characteristic of each volcanic suite broadly evolving through cogenetic magmatic processes. Some of the outstanding features of the isotopic correlation arrays are as follows: (1) NdSr shows an anticorrelation within the field of ocean island basalts, extending from the MORB end-member to an enriched, time-averaged high Rb Sr and Nd Sr end-member (EM1), (2) SrPb also shows an anticorrelation, similar to that of Hawaiian and walvis Ridge basalts, (3) NdPb shows a positive correlation, and (4) the 207Pb 204Pb vs 206Pb 204Pb plot shows linear arrays parallel to the general trend (NHRL) for MORB on both sides of the geochron, although in the 208Pb 204Pb vs 206Pb 204Pb plot the linear array is significantly displaced above the NHRL in a pattern similar to that of the oceanic island basalts that show the Dupal signatures. In all isotope correlation patterns, the data arrays define two different mantle components-a MORB-like component and an enriched mantle component. The isotopic data presented here clearly demonstrate the existence of Dupal compositions in the sources of the continental volcanic rocks of eastern China. We suggest that the subcontinental mantle

  17. Compression Ratio Adjuster

    NASA Technical Reports Server (NTRS)

    Akkerman, J. W.

    1982-01-01

    New mechanism alters compression ratio of internal-combustion engine according to load so that engine operates at top fuel efficiency. Ordinary gasoline, diesel and gas engines with their fixed compression ratios are inefficient at partial load and at low-speed full load. Mechanism ensures engines operate as efficiently under these conditions as they do at highload and high speed.

  18. Offer/Acceptance Ratio.

    ERIC Educational Resources Information Center

    Collins, Mimi

    1997-01-01

    Explores how human resource professionals, with above average offer/acceptance ratios, streamline their recruitment efforts. Profiles company strategies with internships, internal promotion, cooperative education programs, and how to get candidates to accept offers. Also discusses how to use the offer/acceptance ratio as a measure of program…

  19. Detecting isotopic ratio outliers

    SciTech Connect

    Bayne, C.K.; Smith, D.H.

    1985-01-01

    An alternative method is proposed for improving isotopic ratio estimates. This method mathematically models pulse-count data and uses iterative reweighted Poisson regression to estimate model parameters to calculate the isotopic ratios. This computer-oriented approach provides theoretically better methods than conventional techniques to establish error limits and to identify outliers. 6 refs., 3 figs., 3 tabs.

  20. Specialized ratio analysis.

    PubMed

    Wyer, J C; Salzinger, F H

    1983-01-01

    Many common management techniques have little use in managing a medical group practice. Ratio analysis, however, can easily be adapted to the group practice setting. Acting as broad-gauge indicators, financial ratios provide an early warning of potential problems and can be very useful in planning for future operations. The author has gathered a collection of financial ratios which were developed by participants at an education seminar presented for the Virginia Medical Group Management Association. Classified according to the human element, system component, and financial factor, the ratios provide a good sampling of measurements relevant to medical group practices and can serve as an example for custom-tailoring a ratio analysis system for your medical group.

  1. Birthweight ratio revisited.

    PubMed Central

    Brownlee, K G; Ng, P C; Roussounis, S H; Dear, P R

    1991-01-01

    In order to test the hypothesis suggested in a recent report that the birthweight ratio might be a useful predictor of several important clinical outcome measures in babies of less than 31 weeks' gestation, we examined the association between the birthweight ratio and aspects of both short and long term outcome in 436 Leeds babies of less than 31 weeks' gestation. Unlike the report, and contrary to what we had expected, we were unable to find any significant association between birthweight ratio and length of time on the ventilator, mortality, neurological outcome, or intellectual outcome. PMID:2025035

  2. Grand Comore Island: A well-constrained “low 3He/4He” mantle plume

    NASA Astrophysics Data System (ADS)

    Class, Cornelia; Goldstein, Steven L.; Stute, Martin; Kurz, Mark D.; Schlosser, Peter

    2005-05-01

    ratios, indicating that the Grande Comore 3He/ 4He ratios are not significantly influenced by crustal contamination and reflect recent mixing between plume- and lithosphere-derived melts. The lithosphere beneath Grande Comore has retained its MORB-like helium isotopic composition, which suggests that the previously identified amphibole-forming metasomatism of the lithospheric mantle [1] [C. Class, S.L. Goldstein, Plume-lithosphere interactions in the ocean basins: constraints from the source mineralogy. Earth Planet. Sci. Lett., 150 (1997) 245-260] occurred prior to the arrival of the Comoro plume. The well-constrained 3He/ 4He = 5.2 ± 0.2 RA ( 4He/ 3He ≈ 137,000 ± 5000) of the Comoro plume confirms the existence of "low 3He/ 4He" mantle plumes. A global compilation of OIB shows that OIB from "low 3He/ 4He" plumes form one "side" of the roughly triangular distribution of the global OIB data set in 143Nd/ 144Nd versus 206Pb/ 204Pb and 208Pb/ 204Pb, encompassing the lowest Nd to the highest Pb isotope ratios. It is also shown that "low 3He/ 4He" plumes are more enriched in Th and U relative to other plumes.

  3. Discrimination of the Cigarettes Geographical Origin by DRC-ICP-MS Measurements of Pb Isotope Compositions

    NASA Astrophysics Data System (ADS)

    Guo, W.; Hu, S.; Jin, L.

    2014-12-01

    Trace Pb are taken up with the same isotopic ratios as is present in the source soil, and the isotopic composition of Pb could used to reflect these sources and provide powerful indicators of the geographic origin of agriculture products derived from vegetative matter. We developed a simple and high throughput method, which based on DRC-ICP-MS for determination of Pb isotope ratios for discriminating the geographic origin of cigarettes. After acid digestion procedure, the cigarette digested solutions were directly analyzed by ICP-QMS with a DRC pressurized by the non-reactive gas Ne. In the DRC, Ne molecules collision with Pb ions and improves Pb isotope ratios precision 3-fold, which may be due to the collisional dampling smoothes out the ion beam fluctuations. Under the optimum DRC rejection parameter Q (RPq = 0.45), the main matrix components (K, Na, Ca, Mg, Al, Fe etc.) originating from cigarettes were filtered out. Mass discrimination of 208Pb/206Pb ratio in Ne DRC mode increased 0.3% compared to the standard mode, the mass bias due to the in-cell Ne gas collision can be accurately corrected by NIST 981 Pb isotope standard. This method was verified by a tobacco reference material CTV-OTL-2. Results of 208Pb/206Pb and 207Pb/206Pb were 2.0848 ± 0.0028 (2δ) and 0.8452 ± 0.0011 (2δ) for CTA-VTL-2, which were agreed with the literature values (208Pb/206Pb = 2.0884 ± 0.0090 and 207Pb/206Pb = 0.8442 ± 0.0032). The precision of Pb isotope ratios (208Pb/206Pb and 207Pb/206Pb) for the cigarette samples are ranged from 0.01 to 0.08% (N = 5). It has sufficient precision to discriminate 91 different brand cigarettes originated from four different geographic regions (Shown in Fig).

  4. Composition and evolution of submarine volcanic rocks from the central and western Canary Islands

    NASA Astrophysics Data System (ADS)

    Abratis, M.; Schmincke, H.-U.; Hansteen, T. H.

    2002-08-01

    Submarine volcanic rocks dredged during RV Meteor cruise M43-1 comprise alkali basalts, basanites, nephelinites and their differentiates representing both basement-shield and young post-shield volcanics of Gran Canaria, Tenerife, La Palma and El Hierro. The primitive lavas vary widely in trace element composition (e.g., Zr/Y=6.6-11.7, (La/Sm)N=2.3-5.4, and Ba/Yb=71-311), and they are characterized by steep, rare-earth element patterns with mean (La/Yb)N=16, and by pronounced, positive primitive mantle-normalized Nb and Ta and negative K anomalies similar to HIMU-type basalts. Rocks from the submarine flanks west and north of Gran Canaria are isotopically and geochemically identical to rocks of the subaerial Miocene shield stage, but they are distinct from rocks of the post-shield stages (Zr/Nb=6.3-8.9, 87Sr/86Sr=0.70327-0.70332, 143Nd/144Nd=0.51289-0.51293, 206Pb/204Pb=19.55-19.88). Most rocks dredged from the submarine flanks of Tenerife are isotopically and geochemically similar to rocks of the adjacent subaerial shield remnants, but a few resemble rocks of the subaerial post-shield stages (total range in Zr/Nb=4.6-6.1, 87Sr/86Sr=0.70300-0.70329, 143Nd/144Nd=0.51281-0.51292, 206Pb/204Pb=19.51-19.96). Rocks from the southern submarine ridge of La Palma cover the entire compositional range of the subaerial rocks of that ridge. Additionally, they comprise a high Zr/Nb group which resembles rocks of the ca. 1-Ma-old Taburiente shield of northern La Palma (total range in Zr/Nb=3.0-6.4, 87Sr/86Sr=0.70297-0.70314, 143Nd/144Nd=0.51288-0.51296, 206Pb/204Pb=19.21-19.79). Rocks from the southern submarine ridge of El Hierro compositionally resemble subaerial rocks of the island (Zr/Nb=4.1-6.2, 87Sr/86Sr=0.70296-0.70314, 143Nd/144Nd=0.51291-0.51297, 206Pb/204Pb=19.25-19.91). The degree of melting in the subcanarian mantle is interpreted to decrease from east to west across the archipelago whereas the proportion of depleted mantle component in the melting anomaly increases

  5. Geochemical characteristics of basaltic glasses from the AMAR and FAMOUS axial valleys, Mid-Atlantic Ridge (36°-37°N): Petrogenetic implications

    NASA Astrophysics Data System (ADS)

    Frey, F. A.; Walker, N.; Stakes, D.; Hart, S. R.; Nielsen, R.

    1993-03-01

    The axial valley of the Mid-Atlantic Ridge from 36° to 37°N was intensively sampled by submersible during the FAMOUS and AMAR projects. Our research focussed on the compositional and isotopic characteristics of basaltic glasses from the AMAR valley and the NARROWGATE region of the FAMOUS valley. These basaltic glasses are characterized by: (1) major element abundance trends that are consistent with control by multiphase fractionation (olivine, plagioclase and clinopyroxene) and magma mixing, (2) near isotopic homogeneity δ 18O= 5.2to6.4 , 87Sr/ 86Sr= 0.70288to0.70299 and 206Pb/ 204Pb= 18.57to18.84 , and (3) a wide range of incompatible element abundance ratios; e.g., within the AMAR valley chondrite-normalized La/Sm ranges from 0.7 to 1.5 and La/Yb from 0.6 to 1.6. These ratios increase with decreasing MgO content. Because of the limited variations in isotopic ratios of Sr, Nd and Pb, it is plausible that these compositional variations reflect post-melting magmatic processes. However, it is not possible to explain the correlated variation in MgO content and incompatible element abundance ratios, such as La/Sm and Zr/Nb, by fractional crystallization or more complex processes such as boundary layer fractionation. These geochemical trends can be explained by mixing of parental magmas that formed by very different extents of melting. In particular, the factor of three variation in Ce content in samples with ˜ 2.1% Na 2O and 8% MgO requires a component derived by < 1% melting. If the large variations in abundance ratios of incompatible elements reflect the melting process, a large, long-lived magma chamber was not present during eruption of these AMAR lavas. The geological characteristics of the AMAR valley and the compositions of AMAR lavas are consistent with episodic volcanism; i.e., periods of magma eruption were followed by extensive periods of tectonism with little or no magmatism.

  6. Lead isotope compositions of Late Cretaceous and early Tertiary igneous rocks and sulfide minerals in Arizona: Implications for the sources of plutons and metals in porphyry copper deposits

    USGS Publications Warehouse

    Bouse, R.M.; Ruiz, J.; Titley, S.R.; Tosdal, R.M.; Wooden, J.L.

    1999-01-01

    Porphyry copper deposits in Arizona are genetically associated with Late Cretaceous and early Tertiary igneous complexes that consist of older intermediate volcanic rocks and younger intermediate to felsic intrusions. The igneous complexes and their associated porphyry copper deposits were emplaced into an Early Proterozoic basement characterized by different rocks, geologic histories, and isotopic compositions. Lead isotope compositions of the Proterozoic basement rocks define, from northwest to southeast, the Mojave, central Arizona, and southeastern Arizona provinces. Porphyry copper deposits are present in each Pb isotope province. Lead isotope compositions of Late Cretaceous and early Tertiary plutons, together with those of sulfide minerals in porphyry copper deposits and of Proterozoic country rocks, place important constraints on genesis of the magmatic suites and the porphyry copper deposits themselves. The range of age-corrected Pb isotope compositions of plutons in 12 Late Cretaceous and early Tertiary igneous complexes is 206Pb/204Pb = 17.34 to 22.66, 207Pb/204Pb = 15.43 to 15.96, and 208Pb/204Pb = 37.19 to 40.33. These Pb isotope compositions and calculated model Th/U are similar to those of the Proterozoic rocks in which the plutons were emplaced, thereby indicating that Pb in the younger rocks and ore deposits was inherited from the basement rocks and their sources. No Pb isotope differences distinguish Late Cretaceous and early Tertiary igneous complexes that contain large economic porphyry copper deposits from less rich or smaller deposits that have not been considered economic for mining. Lead isotope compositions of Late Cretaceous and early Tertiary plutons and sulfide minerals from 30 metallic mineral districts, furthermore, require that the southeastern Arizona Pb province be divided into two subprovinces. The northern subprovince has generally lower 206Pb/204Pb and higher model Th/U, and the southern subprovince has higher 206Pb/204Pb and

  7. Miocene-Pleistocene magmas in the Monbetsu area, Northeast Hokkaido, tap N-MORB-like sources contaminated by slab-derived fluids

    NASA Astrophysics Data System (ADS)

    Hoang, Nguyen; Miyagi, Isoji; Itoh, Jun'ichi

    2015-05-01

    Cenozoic intraplate volcanism in northern and northeastern Hokkaido appears to have been closely associated with the Late Oligocene to Mid-Miocene opening of the Japan and Okhotsk Seas (c. 23-12 Ma). Between 12 and 2 Ma, volcanism appeared in the Monbetsu area of northeastern Hokkaido, whose magmatic products are characterized by relative depletions in Nb and Ta and enrichments in LILE and Pb, suggesting a subduction-related source. Likewise, their N-MORB-like isotopic affinity resembles that of active arcs in eastern Hokkaido. These geochemical features are distinct from those of intraplate Cenozoic magmas in Sikhote-Alin, Sakhalin and within the Japan Sea itself, which appear to show a secular change from high-87Sr/86Sr, -206Pb/204Pb and low-143Nd/144Nd (EM2-rich) mantle sources to relatively low-87Sr/86Sr and -206Pb/204Pb (EM1-rich) types, resembling the progression of magmatic activity during early stages of Japan Sea opening. The EM2 is interpreted to derive from lithospheric mantle while EM1-like components may have been introduced by material delaminated from the Sino-Korea craton, following the Indo-Eurasia collision. In contrast, the Cenozoic Monbetsu volcanics in northern and northeastern Hokkaido appear to lack any such temporal pattern, implying that their respective source regions have not changed since at least c. 14 Ma. We suggest, accordingly, that upper mantle beneath Hokkaido may have been isolated after opening of the Japan and Okhotsk Seas, to the west and northwest, the Kurile Basin to the northeast, and continuing west-vergent subduction of the Pacific plate. Given the fact that Cenozoic volcanism in north and northeastern Hokkaido shows apparent subduction-related character, and that the relationship between this activity and opening of the Kurile Basin remains unclear, we tentatively conclude that intraplate mantle melting may reflect a combination of effects, that of slab-derived hydrous fluid superimposed on upwelling asthenosphere.

  8. Combined Sr, Nd, Pb and Hf isotopic constraints on the origin of Shatsky Rise (NW Pacific)

    NASA Astrophysics Data System (ADS)

    Geldmacher, J.; Heydolph, K.; Murphy, D. T.; Romanova, I.; Mahoney, J. J.; Hoernle, K.

    2012-12-01

    and 206Pb/204Pb ratios, placing them closer to a composition recently proposed for a non-chondritic, primitive mantle reservoir which is supposed to be preferentially sampled by large igneous province volcanism (Jackson and Carlson, 2011). Expedition 324 Scientists, IODP Prel. Rept. 324, 2010 Jackson, M.G. and Carlson, R.W., Nature, vol. 476, 2011 Sano T., Shimizu K., Ishikawa A., Senda R., Chang Q., Kimura J.-I., Widdowson M., Sager W.W. Geochemistry, Geophysics, Geosystems (in press)

  9. A Recipe for Ratio

    ERIC Educational Resources Information Center

    Moffett, Pamela

    2012-01-01

    Many learners still struggled to appreciate, and understand the difference between, the concepts of fractions and ratio. This is not just a UK phenomenon, which is demonstrated here by the use of a resource developed by the Wisconsin Centre for Education, in association with the Freudenthal Institute of the University of Utrecht, with a group of…

  10. Area Ratios of Quadrilaterals.

    ERIC Educational Resources Information Center

    Anderson, David R.; Arcidiacono, Michael J.

    1989-01-01

    Shows that the ratio of the area of the quadrilateral formed by joining the kth points to the area of the original quadrilateral is constant whether it is convex or concave quadrilateral. Presents many geoboard or dot paper diagrams and geometrical expresssions. (YP)

  11. Temporal variations in the strength of the Antarctic coastal current from the provenance and comminution ages of Weddell Sea sediments

    NASA Astrophysics Data System (ADS)

    Torfstein, A.; McManus, J. F.

    2012-12-01

    The location and geometric setting of the Weddell Sea, one of the large marginal seas of Antarctica, make it a sensitive recorder of the input of subglacial erosion products from Antarctica. We present evidence for variability in the sources and temporal fluxes of Antarctic continental erosion products, based on Pb, Sr and Nd isotopic compositions, U-decay series and trace element concnetrations of sediments deposited over the last ~250 kyrs in the East and deep-North Weddell Sea, at sites PS1388 and PS1170, respectively. Each sediment sample was separated into three grain size fractions of authigenic-free material (>20um, 20-2um, <2um). Significant differences are observed in sediment composition from the two studied regions as well as between grain size fractions within each sample. Lead isotopic compositions show a clear distinction between both sites with 206Pb/204Pb ratios at sites PS1388 and PS1170 ranging between 17.958-18.307 and 18.655-18.939, repsectively. The isotopic composition of Sr is generally similar at both sites, in the range of 0.715-0.723, except for <2um particles from PS1170 that display significantly higher values in the range of 0.726-0.734. The latter also display the strongest 234U-depletion with typical (234U/238U) ratios around 0.8. These observations imply that the clay size fraction in the North Weddell Sea originates from a distant region, most likely East Antarctica, and that it was exposed to more intense weathering and transport processes relative to the coarser particles. Hence, secular variations in 87Sr/86Sr and (234U/238U) ratios provide a sensitive recorder of the the sediments comminution ages (i.e., their time of transport between source and sink) and the intensity of weathering processes they were exposed to. The combined evidence supports enhanced rates of sediment transport by the Antarctic coastal current from the East Antarctic sector to the Weddell Sea during interglacial stages compared to glacial times, with

  12. A Geochemical Study of Magmatic Processes and Evolution along the Submarine Southwest Rift zone of Mauna Loa Volcano, Hawaii

    NASA Astrophysics Data System (ADS)

    Rhodes, J. M.; Garcia, M. O.; Weis, D.; Trusdell, F. A.; Vollinger, M. J.

    2003-12-01

    Mauna Loa's southwest rift zone (SWR) extends for 102 km from its summit caldera, at an elevation of 4,170 m above sea level, to submarine depths of over 4,500 m. About 65% of the rift zone is subaerial and 35% submarine. Recent sampling with the Jason II submersible of the `mile-high' (1800 m) Ka Lae submarine landslide scarp and the deepest section of the rift zone, in conjunction with previous submersible and dredge-haul collecting, provides petrological and geochemical understanding of rift zone processes, as well as a record of Mauna Loa's eruptive history extending back about 400 ka. The major and trace element trends of the submarine lavas are remarkably similar to those of historical and young prehistoric lavas (<31 ka) erupted along the subaerial SWR. We take this to imply that magma-forming processes have remained relatively constant over much of the volcano's recorded eruptive history. However, the distribution of samples along these trends has varied, and is correlated with elevation. There are very few picrites (>12% MgO) among the subaerial lavas, and compositions tend to cluster around 6.8-8.0% MgO. In contrast, picritic lavas are extremely abundant in the submarine samples, increasing in frequency with depth, especially below 1200 m. These observations support earlier interpretations that the submarine lavas are derived directly from deeper levels in the magma column, and that magmas from a shallow, steady-state, magma reservoir are of uncommon at these depths. Isotopic ratios of Pb and Sr in the submarine lavas, in conjunction with Nb/Y and Zr/Nb ratios, extend from values that are identical with subaerial historical Mauna Loa lavas to lavas with markedly lower 87Sr/86Sr and higher 206Pb/204Pb isotopic ratios. As yet, we see no correlation with depth or age, but the implications are that, in the past, the plume source of Mauna Loa magmas was more variable than in the last 31 ka, and contained a greater proportion of the Kea component. *Team members

  13. Precaldera lavas of the southeast San Juan Volcanic Field: Parent magmas and crustal interactions

    NASA Astrophysics Data System (ADS)

    Colucci, M. T.; Dungan, M. A.; Ferguson, K. M.; Lipman, P. W.; Moorbath, S.

    1991-07-01

    Early intermediate composition volcanic rocks of the Oligocene (circa 34-29 Ma) southeast San Juan volcanic field, southern Colorado, comprise the Conejos Formation. Conejos lavas include both high-K calc-alkaline and alkaline magma series (54-69% SiO2) ranging in composition from basaltic andesite (basaltic trachyandesite) to dacite (trachydacite). The subsequent Platoro caldera complex (29-27 Ma) was superimposed on a cluster of broadly precursory Conejos stratocones. Precaldera volcanism occurred in three pulses corresponding to three time-stratigraphic members: (1) the Horseshoe Mountain member, (2) the Rock Creek member, and (3) the Willow Mountain member. Each member exhibits distinctive phenocryst modes and incompatible trace element contents. Horseshoe Mountain lavas (hornblende-phyric) have relatively low alkali and incompatible element abundances, Rock Creek lavas (anhydrous phenocrysts) and ash-flow tuffs have the highest abundances, and Willow Mountain lavas (diverse mineralogy) are intermediate. All Conejos lavas exhibit low ratios of lead (206Pb/204Pb = 17.5 to 18.2) and neodymium (ɛNd = -8 to -4) isotopes and high 87Sr/86Sr (0.7045 to 0.7056) compared to depleted asthenospheric mantle. These values lie between those of likely mantle compositions and the isotopic composition of Proterozoic crust of the southern Rocky Mountains. Mafic lavas of the Horseshoe Mountain member have the lowest Pb and Nd isotope ratios among Conejos members but trend toward higher isotopic values with increasing degrees of differentiation. Compositions within the Rock Creek series trend toward higher Pb and lower Nd isotope ratios with increasing SiO2. Willow mountain volcanic sequences define diverse chemical-isotopic correlations. We interpret the chemical and isotopic differences observed between mafic lavas of each member to reflect derivation from compositionally distinct mantle derived parent magmas that have experienced extensive deep level crustal contamination

  14. Petrogenesis and economic potential of the Erhongwa mafic-ultramafic intrusion in the Central Asian Orogenic Belt, NW China: Constraints from olivine chemistry, U-Pb age and Hf isotopes of zircons, and whole-rock Sr-Nd-Pb isotopes

    NASA Astrophysics Data System (ADS)

    Sun, Tao; Qian, Zhuang-Zhi; Li, Chusi; Xia, Ming-Zhe; Yang, Su-Hong

    2013-12-01

    The Erhongwa mafic-ultramafic intrusion is located in the southern margin of the Central Asian Orogenic Belt in northern Xinjiang where many early-Permian mafic-ultramafic intrusions host important Ni-Cu sulfide deposits. In this paper we report zircon U-Pb age, olivine chemistry and integrated whole-rock chemical and isotopic compositions for the Erhongwa mafic-ultramafic intrusion. This intrusion is composed of lherzolites and gabbroic rocks. The U-Pb age of zircon from a large olivine gabbro sample from the intrusion is 283.1 ± 1.5 Ma, which indicates that the Erhongwa intrusion is contemporaneous with the early-Permian sulfide ore-bearing mafic-ultramafic intrusions in the central Tianshan region. Olivine from the Erhongwa intrusion contains up to 89.5 mol% Fo and 3000 ppm Ni, which are the highest among all known early-Permian mafic-ultramafic intrusions in the region. The occurrence of small sulfide inclusions in the most primitive olivine and significant Ni depletion in more fractionated olivine in the Erhongwa intrusion indicate that sulfide segregation took place during olivine fractional crystallization. The Erhongwa intrusive rocks are characterized by light REE enrichment relative to heavy REE, negative Nb anomalies, positive εNd (t = 283 Ma) values from + 6.3 to + 7.7, low initial 87Sr/86Sr ratios from 0.7034 to 0.7036, initial 206Pb/204Pb ratios from 17.8 to 17.9 and zircon εHf values from 8.0 to 15.5. The Erhongwa mafic-ultramafic rocks and coeval A-type granites in the region have similar isotopic compositions but the former have lower Th/Nb ratios than the latter. These similarities and differences are consistent with the interpretation that the Erhongwa magma formed by the mixing of a mafic magma derived from a depleted mantle with a granitic melt derived from a juvenile arc crust. It is deduced that sulfide saturation in the Erhongwa magmatic system was related to the magma mixing event at depth. More significant sulfide mineralization may

  15. From Purgatory to Paradise: The Volatile Life of Hawaiian Magma

    NASA Astrophysics Data System (ADS)

    Marske, J. P.; Hauri, E. H.; Trusdell, F.; Garcia, M. O.; Pietruszka, A. J.

    2014-12-01

    Variations in radiogenic isotope ratios and magmatic volatile abundances (e.g., CO2 or H2O) in Hawaiian lavas reveal key processes within a deep-seated mantle plume (e.g., mantle heterogeneity, source lithology, partial melting, and magma degassing). Shield-stage Hawaiian lavas likely originate from a mixed plume source containing peridotite and recycled oceanic crust (pyroxenite) based on variations of radiogenic isotopes (e.g., 206Pb/204Pb). The mantle source region may also be heterogeneous with respect to volatile contents, yet the link between pre-eruptive volatile budgets and mantle source lithology in the Hawaiian plume is poorly constrained due to shallow magmatic degassing and mixing. Here, we use a novel approach to investigate this link using Os isotopic ratios, and major, trace, and volatile elements in olivines and mineral-hosted melt inclusions (MIs) from 34 samples from Koolau, Mauna Loa, Hualalai, Kilauea, and Loihi. These samples reveal a strong correlation between volatile contents in olivine-hosted MIs and Os isotopes of the same olivines, in which lavas that originated from greater proportions of recycled oceanic crust/pyroxenite (i.e. 'Loa' chain volcanoes: Koolau, Mauna Loa, Loihi) have MIs with the lower H2O, F, and Cl contents than 'Kea' chain volcanoes (i.e. Kilauea) that contain greater amounts of peridotite in the source region. No correlation is observed with CO2 or S. The depletion of fluid-mobile elements (H2O, F, and Cl) in 'Loa' chain volcanoes indicates ancient dehydrated oceanic crust is a plume component that controls much of the compositional variation of Hawaiian Volcanoes. The presence of dehydrated recycled mafic material in the plume source suggests that subduction effectively devolatilizes the mafic part of the oceanic crust. These results are similar to the observed shifts in H2O/Ce ratios near the Easter and Samoan hotspots [1,2]. Thus, it appears that multiple hotspots may record relative H2O depletions and possibly other

  16. Isotopic and geochemical signatures of Late Quaternary sediments in the Fram Strait area

    NASA Astrophysics Data System (ADS)

    Maccali, J.; Hillaire-Marcel, C.; Carignan, J.; Reisberg, L. C.

    2010-12-01

    isotopic excursions towards lower 206Pb/204Pb ratios at ~ 16 and 20 ka. These short excursions suggest some major possibly short paleogeographical events in the Arctic.

  17. The Pb isotopic evolution of the Martian mantle constrained by initial Pb in Martian meteorites

    NASA Astrophysics Data System (ADS)

    Bellucci, J. J.; Nemchin, A. A.; Whitehouse, M. J.; Snape, J. F.; Bland, P.; Benedix, G. K.

    2015-12-01

    The Pb isotopic compositions of maskelynite and pyroxene grains were measured in ALH84001 and three enriched shergottites (Zagami, Roberts Massif 04262, and Larkman Nunatuk 12011) by secondary ion mass spectrometry. A maskelynite-pyroxene isochron for ALH84001 defines a crystallization age of 4089 ± 73 Ma (2σ). The initial Pb isotopic composition of each meteorite was measured in multiple maskelynite grains. ALH84001 has the least radiogenic initial Pb isotopic composition of any Martian meteorite measured to date (i.e., 206Pb/204Pb = 10.07 ± 0.17, 2σ). Assuming an age of reservoir formation for ALH84001 and the enriched shergottites of 4513 Ma, a two-stage Pb isotopic model has been constructed. This model links ALH84001 and the enriched shergottites by their similar μ value (238U/204Pb) of 4.1-4.6 from 4.51 Ga to 4.1 Ga and 0.17 Ga, respectively. The model employed here is dependent on a chondritic μ value (~1.2) from 4567 to 4513 Ma, which implies that core segregation had little to no effect on the μ value(s) of the Martian mantle. The proposed Pb isotopic model here can be used to calculate ages that are in agreement with Rb-Sr, Lu-Hf, and Sm-Nd ages previously determined in the meteorites and confirm the young (~170 Ma) ages of the enriched shergottites and ancient, >4 Ga, age of ALH84001.

  18. Petrology and geochemistry of lower crustal granulites from the Geronimo Volcanic Field, southeastern Arizona

    SciTech Connect

    Kempton, P.D.; Hawkesworth, C.J. ); Harmon, R.S. ); Moorbath, S. )

    1990-12-01

    Mafic to intermediate composition granulite xenoliths occur in Pliocene to Recent alkali basalts from the Geronimo Volcanic Field (GVF), southeastern Arizona, USA. The range of compositions and mineral assemblages observed suggests that the ultimate derivation of these rocks is from a variety of protoliths and that more than one mechanism has operated during the geologic evolution of the lower crust in this area. Two-pyroxene, two-feldspar granulites (meta-diorites) have major and trace element characteristics similar to estimates of post-Archaen lower crust. Low {sup 143}Nd/{sup 144}Nd values and Proterozoic Nd-depleted-mantle model ages (1.2-1.4 Ga) for these rocks require that Precambrian material exists in the lower crust of southeastern Arizona, either as the meta-diorites themselves or as older crust available for melting during production of the meta-diorite protoliths. K-feldspar-free granulites have more mafic compositions and their trace element characteristics are consistent with a cumulate origin. A negative correlation of {sup 208}Pb/{sup 204}Pb vs. {sup 206}Pb/{sup 204}Pb suggests that the meta-cumulate granulites represent mixing between Basin and Range age lavas with older meta-diorite crust and is, thus, evidence for Cenozoic underplating of the lower crust beneath the Basin and Range.

  19. The plumbotectonic model for Pb isotopic systematics among major terrestrial reservoirs-A case for bi-directional transport

    USGS Publications Warehouse

    Zartman, R.E.; Haines, S.M.

    1988-01-01

    Version IV of plumbotectonics expands and refines the original model of Doe and Zartman (1979) and Zartman and Doe (1981) for explaining Pb (Sr, and Nd) isotopic systematics among major terrestrial reservoirs. A case for bi-directional transport among reservoirs is based on the observed isotopic compositions for different tectonic settings, and finds a rationale in the kinetics of plate tectonics. Chemical fractionation and radioactive decay create isotopic differences during periods of isolation of one reservoir from another, whereas dynamic processes allowing mixing between reservoirs tend to reduce these differences. Observed isotopic characteristics reflect a balance between these opposing tendencies and provide constraints on the extent and timing of fractionation and mixing processes. Plumbotectonics does not require interaction with a lower mantle or core reservoir over most of the Earth's lifetime, and, in fact, achieves a material balance consistent with no such exchange of material. Important evidence of the amount and timing of crustal recycling, and of the residence times of mantle heterogeneities lies in the coupled 207Pb 204Pb-206 Pb 204Pb systematics. We believe that examination of the published data base fully supports our contention of significant bi-directional transport of material among terrestrial reservoirs. Plumbotectonics allows us to explore many aspects of reservoir interaction, and to identify parameters that provide meaningful constraints on mantle-crust differentiation. We put forth a compromise fit to many of the model variables in version IV, which can serve as a reference for future work. ?? 1988.

  20. Two Distinct Sets of Magma Sources in Cretaceous Rocks From Magnet Cove, Prairie Creek, and Other Igneous Centers of the Arkansas Alkaline Province, USA

    NASA Astrophysics Data System (ADS)

    Duke, G. I.; Carlson, R. W.; Eby, G. N.

    2008-12-01

    Two distinct sets of magma sources from the Arkansas alkaline province (~106-89 Ma) are revealed by Sr-Nd-Pb isotopic compositions of olivine lamproites vs. other alkalic rock types, including carbonatite, ijolite, lamprophyres, tephrite, malignite, jacupirangite, phonolite, trachyte, and latite. Isotopic compositions of diamond-bearing olivine lamproites from Prairie Creek and Dare Mine Knob point to Proterozoic lithosphere as an important source, and previous Re-Os isotopic data indicate derivation from subcontinental mantle lithosphere. Both sources were probably involved in lamproite generation. Magnet Cove carbonatites and other alkalic magmas were likely derived from an asthenospheric source. Lamproite samples are isotopically quite different from other rock types in Sr-Nd-Pb isotopic space. Although three lamproite samples from Prairie Creek have a large range of SiO2 contents (40-60 wt %), initial values of ɛNd (-10 to -13), 206Pb/204Pb (16.61-16.81), 207Pb/204Pb (15.34-15.36), and 208Pb/204Pb (36.57-36.76) are low and similar. Only 87Sr/86Sr(i) displays a wide range in the Prairie Creek lamproites (0.70627-0.70829). A fourth lamproite from Dare Mine Knob has the most negative ɛNd(i) of -19. Lamproite isotope values show a significant crustal component and isotopically overlap subalkalic rhyolites from the Black Hills (SD), which assimilated Proterozoic crust. Six samples of carbonatite, ijolite, and jacupirangite from Magnet Cove and Potash Sulphur Springs exhibit the most depleted Sr-Nd isotopic signatures of all samples. For these rock types, 87Sr/86Sr(i) is 0.70352 - 0.70396, and ɛNd(i) is +3.8 - +4.3. Eight other rock types have a narrow range of ɛNd(i) (+1.9 - +3.7), but a wide range of 87Sr/86Sr(i) (0.70424 - 0.70629). These 14 samples comprise a fairly tight cluster of Pb isotopic values: 206Pb/204Pb (18.22-19.23), 207Pb/204Pb (15.54-15.62), and 208Pb/204Pb (38.38-38.94), suggesting very little crustal assimilation. They are most similar to EM-2

  1. Transport and selective uptake of radium into natural clay minerals

    NASA Astrophysics Data System (ADS)

    Hidaka, Hiroshi; Horie, Kenji; Gauthier-Lafaye, Françoise

    2007-12-01

    Understanding of the environmental behavior of Ra is important from the viewpoint of the long-termed repository safety of radioactive waste, but investigation of Ra behavior in natural environment is difficult to detect. We found isotopic evidence of Ra transportation and its selective uptake into clay minerals from Pb isotopic analyses. Illite grains found in calcite veins included in sandstone near the Oklo uranium deposit, Republic of Gabon, show extremely low 207Pb/ 206Pb (˜ 0.0158) isotopic ratios. Although the Pb isotopic ratios of calcite and quartz coexisting with illite indicate the formation age of each component, those of illite do not. In addition, illite grains having low 207Pb/ 206Pb isotopic ratios contain a strongly large amount of Ba (1230 to 6010 ppm) in contrast with low contents of Ba in calcite and quartz (< 0.26 ppm). Considering the chemical similarity between Ba and Ra, the 207Pb/ 206Pb isotopic data suggest an excess of 206Pb due to selective adsorption of 226Ra (and also Ba) into illite grains. This is a very rare example to show evidence of the selective adsorption behavior of Ra from the isotopic excesses of 206Pb, although the adsorption ability of Ra itself in nature was largely reported.

  2. Directional gear ratio transmissions

    NASA Technical Reports Server (NTRS)

    Lafever, A. E. (Inventor)

    1984-01-01

    Epicyclic gear transmissions which transmit output at a gear ratio dependent only upon the input's direction are considered. A transmission housing envelops two epicyclic gear assemblies, and has shafts extending from it. One shaft is attached to a sun gear within the first epicyclic gear assembly. Planet gears are held symmetrically about the sun gear by a planet gear carrier and are in mesh with both the sun gear and a ring gear. Two unidirectional clutches restrict rotation of the first planet gear carrier and ring gear to one direction. A connecting shaft drives a second sun gear at the same speed and direction as the first planet gear carrier while a connecting portion drives a second planet gear carrier at the same speed and direction as the first ring gear. The transmission's output is then transmitted by the second ring gear to the second shaft. Input is transmitted at a higher gear ratio and lower speed for all inputs in the first direction than in the opposite direction.

  3. Geochemical and tectonic implications on plate-interface evolution achieved from high-pressure ultramafic rocks in mélange settings

    NASA Astrophysics Data System (ADS)

    Cannaò, E.; Agostini, S.; Scambelluri, M.; Tonarini, S.

    2014-12-01

    Geochemical studies of fluid-mobile elements (FME) joined with B, Sr and Pb isotopic analyses of high-pressure mélanges terranes help constraining tectonic processes and mass transfer during accretion of slab and suprasubduction mantle in plate-interface domains. Here we focus on ultramafic rocks from two plate interface settings: (I) metasediment-dominated mélange (Cima di Gagnone, CdG, Adula Unit), where eclogite-facies de-serpentinized garnet peridotite and chlorite harzburgite lenses are embedded in paraschist; (II) dominated by high-pressure serpentinite (Erro-Tobbio, ET, and Voltri Units, VU, Ligurian Alps). CdG metaperidotite shows low [B], negative δ 11B and high Sr and Pb isotopic ratios. As, Sb loss from metasediment and gain by garnet and chlorite metaperidotite points to exchange between the two systems. Presence of As and Sb in eclogite-facies peridotite minerals and preferential low-T mobility of such elements suggest that exchange was during early subduction burial and prior to eclogitization. Based on high [B], positive δ11B, oxygen and hydrogen isotope, the ET serpentinties were recently interpreted as supra-subduction mantle flushed by slab fluids (Scambelluri & Tonarini, 2012, Geology, 40, 907-910). Their 206Pb/204Pb and 87Sr/86Sr isotope ratios range between 18.300-18.514 and 0.7048-0.7060, respectively. Compared with ET rocks, VU serpentinites have higher As, Sb (up to 1.3 and 0.39 ppm, respectively) and are enriched in radiogenic Sr (up to 0.7105 87Sr/86Sr). This signature reflects interaction with fluids that exchanged with sedimentary rocks, either in outer rise environments or during accretion atop the slab. In the above cases, the serpentinized mantle rocks fingerprint interaction with fluids from different sources, indicating a timing of accretion to plate interface domains. We provide evidence that serpentinized mantle slices of different size and provenance (slab or wedge) accreted to plate interface domains since early subduction

  4. Petrogenesis of postcollisional magmatism at Scheelite Dome, Yukon, Canada: Evidence for a lithospheric mantle source for magmas associated with intrusion-related gold systems

    USGS Publications Warehouse

    Mair, John L.; Farmer, G. Lang; Groves, David I.; Hart, Craig J.R.; Goldfarb, Richard J.

    2011-01-01

    The type examples for the class of deposits termed intrusion-related gold systems occur in the Tombstone-Tungsten belt of Alaska and Yukon, on the eastern side of the Tintina gold province. In this part of the northern Cordillera, extensive mid-Cretaceous postcollisional plutonism took place following the accretion of exotic terranes to the continental margin. The most cratonward of the resulting plutonic belts comprises small isolated intrusive centers, with compositionally diverse, dominantly potassic rocks, as exemplified at Scheelite Dome, located in central Yukon. Similar to other spatially and temporally related intrusive centers, the Scheelite Dome intrusions are genetically associated with intrusion-related gold deposits. Intrusions have exceptional variability, ranging from volumetrically dominant clinopyroxene-bearing monzogranites, to calc-alkaline minettes and spessartites, with an intervening range of intermediate to felsic stocks and dikes, including leucominettes, quartz monzonites, quartz monzodiorites, and granodiorites. All rock types are potassic, are strongly enriched in LILEs and LREEs, and feature high LILE/HFSE ratios. Clinopyroxene is common to all rock types and ranges from salite in felsic rocks to high Mg augite and Cr-rich diopside in lamprophyres. Less common, calcic amphibole ranges from actinolitic hornblende to pargasite. The rocks have strongly radiogenic Sr (initial 87Sr/86Sr from 0.711-0.714) and Pb isotope ratios (206Pb/204Pb from 19.2-19.7), and negative initial εNd values (-8.06 to -11.26). Whole-rock major and trace element, radiogenic isotope, and mineralogical data suggest that the felsic to intermediate rocks were derived from mafic potassic magmas sourced from the lithospheric mantle via fractional crystallization and minor assimilation of metasedimentary crust. Mainly unmodified minettes and spessartites represent the most primitive and final phases emplaced. Metasomatic enrichments in the underlying lithospheric mantle

  5. Mantle flow deduced from geochemical variations in alkaline magmas of HIMU affinity from continent to ocean, northwestern Ross Sea, Antarctica

    NASA Astrophysics Data System (ADS)

    Castillo, P. R.; Panter, K. S.; McIntosh, W. C.

    2011-12-01

    Cenozoic alkaline magmatism in the northwestern Ross Sea (NWRS) region has been recently expanded to include numerous volcanic seamounts on the continental shelf and hundreds more located within the oceanic Adare Basin [1]. The seamounts are Pliocene in age and petrogenetically akin to volcanism on land in the West Antarctic rift system. In general, trace element and Sr-Nd-Pb isotopic data resemble those from ocean islands with HIMU affinity. Apart from the well studied Cameroon volcanic line in West Africa, the NWRS is a unique setting for comparing contemporary alkaline volcanism bridging the transition from oceanic to thinned continental lithosphere adjacent to the thick East Antarctic craton. The geochemistry of NWRS basalts, extending to the northeast from the Mariner Glacier to the Adare Peninsula and into the Adare Basin (~168°E 73°S to ~173°E 70°S), shows a remarkable orderly increase in degree of silica-undersaturation, P2O5, Nb, Zr, Sr contents and La/Yb, Nb/Y, 143Nd/144Nd and 206Pb/204Pb ratios, coupled with a decrease in Ba/La and 87Sr/86Sr ratios, suggesting they were generated from a common heterogeneous mantle source at progressively smaller melt fractions from land to sea. Geochemical variations coincide with northward age propagation in magmatism and southward increase in rifting since the middle Miocene [2]. We propose that the HIMU-like signature in both continental and oceanic sectors is derived from metasomatized lithosphere, whereby the most easily fusible components contribute to the smaller degree melts in greater proportions ocean-ward. Melting may have been triggered by influx of warm asthenosphere initially beneath the continent and then northward by edge-driven convection and channelized by focused extension [3] into the Adare Basin where the metasomatized source is more dispersed. [1] Panter & Castillo (2008) USGS Open-File Report 2007-1047, 069. [2] Granot et al. (2010) Geochem. Geophys. Geosyst. 11(8). [3] Huerta & Harry (2007

  6. Formation of PGM-Cu-Ni deposits in the process of evolution of flood-basalt magmatism in the Noril'sk region

    NASA Astrophysics Data System (ADS)

    Krivolutskaya, N. A.

    2011-08-01

    all. New data on isotopic compositions of Sr (87Sr/86Sr)251 = 0.7089 and Pb (206Pb/204Pb = 20.877-24.528 in anhydrite confirm that local assimilation did not play a substantial role in the formation of rock and ores. On the basis of chemical composition of ore-forming intrusions, their isotopic characteristics, and the composition of melt inclusions in olivine, it is suggested that the lower crustal rocks were a major source of ore-bearing magmas.

  7. Regional Geochemical Trends in Young Basalts Along the Central Anatolian Fault Zone, Turkey

    NASA Astrophysics Data System (ADS)

    Pickard, M.; Furman, T.; Hanan, B. B.; Kurkcuoglu, B.; Sayit, K.

    2009-12-01

    toward the leading edge of the African plate, i.e., to the south. Here we present new Pb and Hf isotopic data on recent (<15 Ma) mafic lavas along the CAFZ previously analyzed for major and trace elements. Isotopic ratios show greater source heterogeneity than suggested by the trace element data and show no apparent relationship with latitude. The Pb-Pb isotope ratios define a data field similar to modern oceanic sediment, intermediate in composition to Western Anatolia SCLM and the C component and enriched Central Atlantic MORB. In the 206Pb/204Pb-ɛHf diagram the Central Anatolian lavas are consistent with mixing between a C-like component on the enriched end of the Central Atlantic MORB trend, and Western Anatolia-like SCLM. The isotopic data support a mixing model between oceanic mantle and subduction modified SCLM sources.

  8. U-Pb (zircon) and geochemical constraints on the age, origin, and evolution of Paleozoic arc magmas in the Oyu Tolgoi porphyry Cu-Au district, southern Mongolia

    USGS Publications Warehouse

    Wainwright, A.J.; Tosdal, R.M.; Wooden, J.L.; Mazdab, F.K.; Friedman, R.M.

    2011-01-01

    Uranium-Pb (zircon) ages are linked with geochemical data for porphyry intrusions associated with giant porphyry Cu-Au systems at Oyu Tolgoi to place those rocks within the petrochemical framework of Devonian and Carboniferous rocks of southern Mongolia. In this part of the Gurvansayhan terrane within the Central Asian Orogenic Belt, the transition from Devonian tholeiitic marine rocks to unconformably overlying Carboniferous calc-alkaline subaerial to shallow marine volcanic rocks reflects volcanic arc thickening and maturation. Radiogenic Nd and Pb isotopic compositions (??Nd(t) range from +3.1 to +7.5 and 206Pb/204Pb values for feldspars range from 17.97 to 18.72), as well as low high-field strength element (HFSE) contents of most rocks (mafic rocks typically have <1.5% TiO2) are consistent with magma derivation from depleted mantle in an intra-oceanic volcanic arc. The Late Devonian and Carboniferous felsic rocks are dominantly medium- to high-K calc-alkaline and characterized by a decrease in Sr/Y ratios through time, with the Carboniferous rocks being more felsic than those of Devonian age. Porphyry Cu-Au related intrusions were emplaced in the Late Devonian during the transition from tholeiitic to calc-alkaline arc magmatism. Uranium-Pb (zircon) geochronology indicates that the Late Devonian pre- to syn-mineral quartz monzodiorite intrusions associated with the porphyry Cu-Au deposits are ~372Ma, whereas granodiorite intrusions that post-date major shortening and are associated with less well-developed porphyry Cu-Au mineralization are ~366Ma. Trace element geochemistry of zircons in the Late Devonian intrusions associated with the porphyry Cu-Au systems contain distinct Th/U and Yb/Gd ratios, as well as Hf and Y concentrations that reflect mixing of magma of distinct compositions. These characteristics are missing in the unmineralized Carboniferous intrusions. High Sr/Y and evidence for magma mixing in syn- to late-mineral intrusions distinguish the Late

  9. Pb-isotopic Features of Primitive Rocks from Hess Deep: Distinguishing between EPR and Cocos-Nazca Mantle Source(s)

    NASA Astrophysics Data System (ADS)

    Jean, M. M.; Falloon, T.; Gillis, K. M.

    2014-12-01

    We have acquired high-precision Pb-isotopic signatures of primitive lithologies (basalts/gabbros) recovered from IODP Expedition 345.The Hess Deep Rift, located in the vicinity of the Galapagos triple junction (Cocos, Nazca, and Pacific), is viewed as one the best-studied tectonic windows into fast-spreading crust because a relatively young (<1.5 Ma) cross section of oceanic crust. This allows for (1) characterization of the mantle source(s) at Hess Deep, (2) insight into the extent of isotopic homogeneity or heterogeneity in the area, and (3) constrain the relative contributions from the intruding Cocos-Nazca spreading center. The observed Pb-isotopic variation at Hess Deep covers almost the entire range of EPR MORB (10°N to -5°S). Hess Deep samples range from 208Pb (37.3-38.25), 207Pb (15.47-15.58), 206Pb (17.69-18.91). These compositions suggest that this part of Hess Deep mantle is no more isotopically homogeneous than EPR mantle. Two distinct arrays are also observed: 208Pb-enriched (r2=0.985; n=30) and 208Pb-depleted (r2=0.988; n=6). The 208Pb/204Pb isotopes indicates that the Pb-source for some of the samples at Hess Deep had very low Th/U ratios, whereas other areas around the Galapagos microplate seem to ha