Sample records for hf isotope composition

  1. Hf isotopic compositions of the standard zircons for U-Pb dating

    Institute of Scientific and Technical Information of China (English)

    XU Ping; WU Fuyuan; XIE Liewen; YANG Yueheng


    Using the newly published Yb isotopic abundances and the mass bias relationship between Yb and Hf, we carried out an analysis of Hf isotopes in the standard zircon 91500 by means of 193 nm laser attached to Neptune multi-collector ICP-MS (LA-MC-ICPMS). The obtained Hf isotopic data, in either in situ or line scan modes, are not only identical for different spot sizes, but also are consistent with previously published results obtained on TIMS or other MC-ICPMS machines within errors. This indicates that it is possible to obtain reliable 176Hf/177Hf isotopic ratios for zircon in either in situ or line scan conditions on LA-MC-ICPMS machine, and the applied procedures in our study for elemental interfering correction are appropriate for the purpose of acquiring satisfactory accuracy for Hf isotope analyses. The Hf isotopic compositions of four zircon standards in high spatial resolution U-Pb dating, 91500, CZ3,CN92-1 and TEMORA, are measured, respectively. The obtained 176Hf/177Hf ratios are 0.282316+4 (n = 34, 2σ) for 91500, 0.281704±6 (n = 16, 2σ) for CZ3, 0.282200±6 (n = 20,2σ-) for CN92-1 and 0.282684±14 (n = 24, 2σ) for TEMORA,respectively, with 176Lu/177Hf ratios of ~0.00031, 0.000036,0.00083 and 0.00127. Zircons 91500 and CZ3 show narrower variations in 176Hf/177Hf and 176Lu/177Hf ratios than those of zircons CN92-1 and TEMORA, and thus are appropriate standards for the Hf isotope analysis.

  2. Numerical modeling of radioactive neutron capture influence of Hf isotopic composition dynamics rate in the RBMK-1500 reactor

    CERN Document Server

    Jurkevicius, A; Auzelyte, V; Remeikis, V


    The nuclide composition of the nuclear fuel and isotopic composition of the hafnium in the radial neutron flux detectors of the RBMK-1500 reactor were numerically modelled. The sequence SAS2 from package SCALE 4.3 was used for calculations. The nuclear fuel nuclide concentrations, the concentration of Hf isotopes, the neutron absorption rate on Hf isotopes and summary absorption rate dependences on the fuel assembly burn up are presented. (author)

  3. U-Pb ages and Hf isotope compositions of zircons in plutonic rocks from the central Famatinian arc, Argentina (United States)

    Otamendi, Juan E.; Ducea, Mihai N.; Cristofolini, Eber A.; Tibaldi, Alina M.; Camilletti, Giuliano C.; Bergantz, George W.


    The Famatinian arc formed around the South Iapetus rim during the Ordovician, when oceanic lithosphere subducted beneath the West Gondwana margin. We present combined in situ U-Th-Pb and Lu-Hf isotope analyses for zircon to gain insights into the origin and evolution of Famatinian magmatism. Zircon crystals sampled from four intermediate and silicic plutonic rocks confirm previous observations showing that voluminous magmatism took place during a relatively short pulse between the Early and Middle Ordovician (472-465 Ma). The entire zircon population for the four plutonic rocks yields coherent εHf negative values and spreads over several ranges of initial εHf(t) units (-0.3 to -8.0). The range of εHf units in detrital zircons of Famatinian metasedimentary rocks reflects a prolonged history of the cratonic sources during the Proterozoic to the earliest Phanerozoic. Typical tonalites and granodiorites that contain zircons with evolved Hf isotopic compositions formed upon incorporating (meta)sedimentary materials into calc-alkaline metaluminous magmas. The evolved Hf isotope ratios of zircons in the subduction related plutonic rocks strongly reflect the Hf isotopic character of the metasedimentary contaminant, even though the linked differentiation and growth of the Famatinian arc crust was driven by ascending and evolving mantle magmas. Geochronology and Hf isotope systematics in plutonic zircons allow us understanding the petrogenesis of igneous series and the provenance of magma sources. However, these data could be inadequate for computing model ages and supporting models of crustal evolution.

  4. Changes in erosion and ocean circulation recorded in the Hf isotopic compositions of North Atlantic and Indian Ocean ferromanganese crusts (United States)

    Piotrowski, Alexander M.; Lee, Der-Chuen; Christensen, John N.; Burton, Kevin W.; Halliday, Alex N.; Hein, James R.; Günther, Detlef


    High-resolution Hf isotopic records are presented for hydrogenetic Fe–Mn crusts from the North Atlantic and Indian Oceans. BM1969 from the western North Atlantic has previously been shown to record systematically decreasing Nd isotopic compositions from about 60 to ∼4 Ma, at which time both show a rapid decrease to unradiogenic Nd composition, thought to be related to the increasing influence of NADW or glaciation in the northern hemisphere. During the Oligocene, North Atlantic Hf became progressively less radiogenic until in the mid-Miocene (∼15 Ma) it reached +1. It then shifted gradually back to an ϵHf value of +3 at 4 Ma, since when it has decreased rapidly to about −1 at the present day. The observed shifts in the Hf isotopic composition were probably caused by variation in intensity of erosion as glaciation progressed in the northern hemisphere. Ferromanganese crusts SS663 and 109D are from about 5500 m depth in the Indian Ocean and are now separated by ∼2300 km across the Mid-Indian Ridge. They display similar trends in Hf isotopic composition from 20 to 5 Ma, with the more northern crust having a composition that is consistently more radiogenic (by ∼2 ϵHf units). Paradoxically, during the last 20 Ma the Hf isotopic compositions of the two crusts have converged despite increased separation and subsidence relative to the ridge. A correlatable negative excursion at ∼5 Ma in the two records may reflect a short-term increase in erosion caused by the activation of the Himalayan main central thrust. Changes to unradiogenic Hf in the central Indian Ocean after 5 Ma may alternatively have been caused by the expanding influence of NADW into the Mid-Indian Basin via circum-Antarctic deep water or a reduction of Pacific flow through the Indonesian gateway. In either case, these results illustrate the utility of the Hf isotope system as a tracer of paleoceanographic changes, capable of responding to subtle changes in erosional regime not readily resolved

  5. Meteorite zircon constraints on the bulk Lu-Hf isotope composition and early differentiation of the Earth. (United States)

    Iizuka, Tsuyoshi; Yamaguchi, Takao; Hibiya, Yuki; Amelin, Yuri


    Knowledge of planetary differentiation is crucial for understanding the chemical and thermal evolution of terrestrial planets. The (176)Lu-(176)Hf radioactive decay system has been widely used to constrain the timescales and mechanisms of silicate differentiation on Earth, but the data interpretation requires accurate estimation of Hf isotope evolution of the bulk Earth. Because both Lu and Hf are refractory lithophile elements, the isotope evolution can be potentially extrapolated from the present-day (176)Hf/(177)Hf and (176)Lu/(177)Hf in undifferentiated chondrite meteorites. However, these ratios in chondrites are highly variable due to the metamorphic redistribution of Lu and Hf, making it difficult to ascertain the correct reference values for the bulk Earth. In addition, it has been proposed that chondrites contain excess (176)Hf due to the accelerated decay of (176)Lu resulting from photoexcitation to a short-lived isomer. If so, the paradigm of a chondritic Earth would be invalid for the Lu-Hf system. Herein we report the first, to our knowledge, high-precision Lu-Hf isotope analysis of meteorite crystalline zircon, a mineral that is resistant to metamorphism and has low Lu/Hf. We use the meteorite zircon data to define the Solar System initial (176)Hf/(177)Hf (0.279781 ± 0.000018) and further to identify pristine chondrites that contain no excess (176)Hf and accurately represent the Lu-Hf system of the bulk Earth ((176)Hf/(177)Hf = 0.282793 ± 0.000011; (176)Lu/(177)Hf = 0.0338 ± 0.0001). Our results provide firm evidence that the most primitive Hf in terrestrial zircon reflects the development of a chemically enriched silicate reservoir on Earth as far back as 4.5 billion years ago.

  6. Early Paleozoic ridge subduction in the Chinese Altai: Insight from the abrupt change in zircon Hf isotopic compositions

    Institute of Scientific and Technical Information of China (English)


    Zircons were separated from granitoids, gneisses, and sedimentary rocks of the Chinese Altai. Those with igneous characteristics yielded U-Pb ages of 280-2800 Ma, recording a long history of magmatic activity in the region. Zircon Hf isotopic compositions show an abrupt change at ~420 Ma, indicating that prior to that time the magmas came from both ancient and juvenile sources, whereas younger magmas were derived mainly from juvenile material. This may imply that the lithosphere was signifi- cantly modified in composition by a rapid addition of melt from the mantle. We suggest that this dramatic change was due to the onset of ridge subduction, which can account not only for the formation of voluminous granitoids, mafic rocks with complex compositions, and the association of adakite + high-Mg andesite + boninite + Nb-enriched basalt, but also for the coeval high-T, low-P metamorphism.

  7. Early Paleozoic ridge subduction in the Chinese Altai:Insight from the abrupt change in zircon Hf isotopic compositions

    Institute of Scientific and Technical Information of China (English)

    SUN Min; LONG XiaoPing; CAI KeDa; JIANG YingDe; WANG BuYun; YUAN Chao; ZHAO GuoChun; XIAO WenJiao; WU FuYuan


    Zircons were separated from granitoids,gneisses,and sedimentary rocks of the Chinese Altai.Those with igneous characteristics yielded U-Pb ages of 280-2800 Ma,recording a long history of magmatic activity in the region.Zircon Hf isotopic compositions show an abrupt change at ~420 Ma,indicating that prior to that time the magmas came from both ancient and juvenile sources,whereas younger magmas were derived mainly from juvenile material.This may imply that the lithosphere was significantly modified in composition by a rapid addition of melt from the mantle.We suggest that this dramatic change was due to the onset of ridge subduction,which can account not only for the formation of voluminous granitoids,mafic rocks with complex compositions,and the association of adakite + high-Mg andesite+boninite + Nb-enriched basalt,but also for the coeval high-T,Iow-P metamorphism.

  8. Effects of Continental Weathering and Sedimentary Sorting on the Hf, Nd, and Pb Isotopic Composition of Sediments and Implications for Dissolved Input to the Ocean (United States)

    van de Flierdt, T.; Hemming, S. R.; Goldstein, S. L.


    The application of radiogenic isotopes of dissolved trace metals (Hf, Pb, Nd) in the ocean to study climate induced weathering changes on the continents is a relatively new and exciting field of research. Most studies on the radiogenic isotope composition of past seawater are based on chemical sediments such as ferromanganese crusts, and suggest a strong linkage in changes in the style of weathering (chemical vs. physical/glacial) on the continents and the isotopic composition of seawater for elements such as Hf and Pb. This is evidenced by records from the northwest Atlantic, which show significant changes in the Hf and Pb isotopic composition of seawater associated with the onset of Northern Hemisphere Glaciation (NHG) over the past 3 Myr. On the other hand, the impact of glacial weathering on the Nd isotopic composition of seawater is generally thought to be negligible. In order to better understand the systematics and mechanisms of weathering, erosion, and run-off, as well as their bearing on the isotopic composition of the ocean we choose the following strategy: sediments from the Amerilik and Gothabs Fjords near Nuuk (Greenland) have been analyzed for their bulk rock and grain size specific Hf, Nd, and Pb isotopic compositions (sand, silt, mud). Both Fjords are surrounded by early Archean gneisses, among the oldest rocks on Earth, and are filled with glacially floured sediments. Precambrian rocks surround a large fraction of the circum-North Atlantic area that was covered by ice sheets during the NHG, and the source rocks in this region are the most extreme examples. Current knowledge about the impact of weathering processes on isotope systematics implies that the largest changes in the Hf (and Pb) isotopic composition of seawater are expected to arise from glacial weathering of old continental sources. Our data reveal large differences in grain size specific isotope ratios, e.g. between the mud and sand fractions, for sediments with an old provenance

  9. U-Pb isotopic ages and Hf isotope composition of zircons in Variscan gabbros from central Spain: evidence of variable crustal contamination (United States)

    Villaseca, Carlos; Orejana, David; Belousova, Elena; Armstrong, Richard A.; Pérez-Soba, Cecilia; Jeffries, Teresa E.


    Ion microprobe U-Pb analyses of zircons from three gabbroic intrusions from the Spanish Central System (SCS) (Talavera, La Solanilla and Navahermosa) yield Variscan ages (300 to 305 Ma) in agreement with recent studies. Only two zircon crystals from La Solanilla massif gave slightly discordant Paleoproterozoic ages (1,848 and 2,010 Ma). Hf isotope data show a relatively large variation with the juvenile end-members showing ɛHfi values as high as +3.6 to +6.9 and +1.5 to +2.9 in the Navahermosa and Talavera gabbros, respectively. These positive ɛHfi values up to +6.9 might represent the composition of the subcontinental mantle which generates these SCS gabbros. This ɛHfi range is clearly below depleted mantle values suggesting the involvement of enriched mantle components on the origin of these Variscan gabbros, and is consistent with previous whole-rock studies. The presence of zircons with negative ɛHfi values suggest variable, but significant, crustal contamination of the gabbros, mainly by mixing with coeval granite magmas. Inherited Paleoproterozoic zircons of La Solanilla gabbros have similar trace element composition (e.g. Th/U ratios), but more evolved Hf-isotope signatures than associated Variscan zircons. Similar inherited ages have been recorded in zircons from coeval Variscan granitoids from the Central Iberian Zone. Granitic rocks have Nd model ages (TDM) predominantly in the range of 1.4 to 1.6 Ga, suggesting a juvenile addition during the Proterozoic. However, Hf crustal model ages of xenocrystic Proterozoic zircons in La Solanilla gabbro indicate the presence of reworked Archean protoliths (TDM2 model ages of 3.0 to 3.2 Ga) incorporated into the hybridized mafic magma.

  10. Distribution Coefficients of Elements on TODGA Resin in HNO3, HCl and HF: Application to Determination of Lu/Hf Ratio and Hf Isotopic Composition in Meteorites (United States)

    Pourmand, A.; Dauphas, N.


    Distribution coefficients for 60 elements on TODGA resin are presented along with a robust single-column protocol for separation of HSFE, lanthanides and actinides in meteorites and terrestrial rocks for high-precision isotope analysis.

  11. Zircon-apatite U-Pb geochronology, zircon Hf isotope composition and geochemistry of granite batholith in the northern Mexico: Implications for Tectonomagmatic evolution of southern Cordillera. (United States)

    Mahar, M. A.; Goodell, P.


    We present the zircon-apatite U-Pb ages and zircon Hf isotope composition of the granite batholith exposed at the western boundary of Chihuahua. Granidiorite samples were analyzed from both, north and south of the Rio El Fuerte and Sinforosa Lineament. Based on previous studies, the WWN-EES trending Sinforosa Lineament is proposed as the manifestation of a terrane boundary between Seri in the north and Tahue terrane in the south. Zircon U-Pb data indicate that the magmatism spans a time period of 36 Ma from 89 to 53 Ma to the north of the Sinforosa Lineament while granodiorites in the south of the Sinforosa Lineament are dated at 59 Ma. The U-Pb apatite ages are variable in the north of the Sinforosa Lineament and range from 86-51 Ma. These apatite dates are 1-28 Ma younger than the corresponding zircon U-Pb crystallization ages. This indicates variable cooling rates and moderate to shallow emplacement. In contrast, in the south of the Sinforosa Lineament, the U-Pb apatite ages (64-59 Ma) are indistinguishable from the zircon U-Pb age (59 Ma), indicating rapid cooling and shallow emplacement. Zircon morphology and U-Pb dating revealed the absence of inherited component in the zircon ages, as no inheritance of any age has been observed. Most of the northwestern Mexico is underlain by Precambrian-Paleozoic-Jurassic basement. However, in the study area, U-Pb dating does not support the involvement of the older basement in generating the granite magmas. The weighted mean initial ɛHf (t) isotope composition of granodiorites on both sides of the Sinforosa Lineament varies from +2 to +5. However, Hf isotope composition in the south of the Sinforosa Lineament is more heterogeneous and relatively evolved with weighted Mean ɛHf (t) = +1.45. The Hf isotope composition is consistent with the previously reported near bulk silicate Sr-Nd isotope values. We suggest that the magmatic rocks in this region are not derived from melting of a felsic older crust beneath the batholith

  12. Zircon U-Pb geochronology, Sr-Nd-Hf isotopic composition and geological significance of the Late Triassic Baijiazhuang and Lvjing granitic plutons in West Qinling Orogen (United States)

    Duan, Meng; Niu, Yaoling; Kong, Juanjuan; Sun, Pu; Hu, Yan; Zhang, Yu; Chen, Shuo; Li, Jiyong


    The Qinling Orogen was a consequence of continental collision of the South China Craton with the North China Craton in the Triassic and caused widespread granitoid magmatism. However, the petrogenesis of these granitoids remains controversial. In this paper, we choose the Baijiazhuang (BJZ) and Lvjing (LJ) plutons in the West Qinling Orogen for a combined study of the zircon U-Pb geochronology, whole-rock major and trace element compositions and Sr-Nd-Hf isotopic characteristics. We obtained zircon crystallization ages of 216 Ma and 212 Ma for the BJZ and the LJ plutons, respectively. The granitoid samples from both plutons have high K2O metaluminous to peraluminous compositions. They are enriched in large ion lithophile elements (LILEs), light rare earth elements (LREEs) and depleted in high field-strength elements (HFSEs) with significant negative Eu anomalies. The BJZ samples have initial Sr isotopic ratios of 0.7032 to 0.7078, εNd(t) of - 10.99 to - 8.54 and εHf (t) of - 10.22 to - 6.41. The LJ granitoids have initial Sr isotopic ratios of 0.7070 to 0.7080, εNd(t) of - 5.37 to - 4.58 and εHf(t) of - 3.64 to - 1.78. The enriched isotopic characteristics of the two plutons are consistent with their source being dominated by ancient continental crust. However, two BJZ samples show depleted Sr isotope compositions, which may infer possible involvement of mantle materials. Mantle-derived melt, which formed from partial melting of mantle wedge peridotite facilitated by dehydration of the subducted/subducting Mianlue ocean crust, provide the required heat for the crustal melting while also contributing to the compositions of these granitoids. That is, the two granitic plutons are magmatic responses to the closure of the Mianlue ocean basin and the continental collision between the Yangtze and South Qinling crustal terranes.

  13. Decoupling of whole-rock Nd-Hf and zircon Hf-O isotopic compositions of a 284 Ma mafic-ultramafic intrusion in the Beishan Terrane, NW China (United States)

    Su, Ben-Xun; Qin, Ke-Zhang; Lu, Ying-Huai; Sun, He; Sakyi, Patrick Asamoah


    Abundant Permian mafic-ultramafic intrusions in the Beishan Terrane, NW China, are parts of the Tarim large igneous province. Among these intrusions, Luodong intrusion is composed of dunite, wehrlite and gabbro. These rocks have whole-rock Sr-Nd-Hf and zircon Hf-O isotope compositions that display significant decoupling. The decoupling of these generally well-correlated systems demonstrates contrasting evolving trends. Systematic compositional and mineralogical controls on decoupling have been investigated. Wehrlites and gabbros show MORB-like trace element patterns with negligible crustal contamination. They have high initial 143Nd/144Nd [ɛNd(t) = +6.6 to +11.2] and 176Hf/177HfHf(t) = +12.2 to +16.9] and low initial 87Sr/86Sr [(87Sr/86Sr)i = 0.702949-0.704098] ratios and plot within the MORB field, indicating that their parental magmas were derived from a depleted mantle source. The enrichment features are present in the zircon crystals separated from the gabbro. These homogeneously unzoned zircon crystals have high U concentrations, low Th/U ratios and a U-Pb age of 284.0 ± 2.3 Ma. They are therefore interpreted as having formed rapidly in a highly fractionated/evolved magma. Their ɛHf(t) and δ18O values range from -9.3 to -6.7 and +10.25 ‰ to +11.42 ‰, respectively. The decoupling is linked with crustal contamination by ancient crust (probably Proterozoic schist in the Beishan Terrane) that occurred during zircon crystallization. However, the contamination signature in the whole-rock composition was soon overprinted by magma mixing process. The inference is evidenced by zoning textures preserved in plagioclase, clinopyroxene, spinel and particularly olivine, and the presence of coeval diabase dykes cutting through the intrusion. The isotope decoupling observed in this mantle-plume-related mafic-ultramafic intrusion supports the idea that Nd-Hf decoupling and Lu/Hf and Sm/Nd parent/daughter variations exist only on a small hand-size scale in a

  14. Water mass circulation and weathering inputs in the Labrador Sea based on coupled Hf-Nd isotope compositions and rare earth element distributions (United States)

    Filippova, Alexandra; Frank, Martin; Kienast, Markus; Rickli, Jörg; Hathorne, Ed; Yashayaev, Igor M.; Pahnke, Katharina


    The Labrador Sea is one of the key areas for deep water formation driving the Atlantic thermohaline circulation and thus plays an important role in Northern Hemisphere climatic fluctuations. In order to better constrain the overturning processes and the origins of the distinct water masses, combined dissolved Hf-Nd isotopic compositions and rare earth element (REE) distribution patterns were obtained from four water depth profiles along a section across the Labrador Sea. These were complemented by one surface sample off the southern tip of Greenland, three shallow water samples off the coast of Newfoundland, and two deep water samples off Nova Scotia. Although light REEs are markedly enriched in the surface waters off the coast of Newfoundland compared to north Atlantic waters, the REE concentration profiles are essentially invariant throughout the water column across the Labrador Sea. The hafnium concentrations of surface waters exhibit a narrow range between 0.6 and 1 pmol/kg but are not significantly higher than at depth. Neodymium isotope signatures (ɛNd) vary from unradiogenic values between -16.8 and -14.9 at the surface to more radiogenic values near -11.0 at the bottom of the Labrador Sea mainly reflecting the advection of the Denmark Strait Overflow Water and North East Atlantic Deep Water, the signatures of which are influenced by weathering contributions from Icelandic basalts. Unlike Nd, water column radiogenic Hf isotope signatures (ɛHf) are more variable representing diverse weathering inputs from the surrounding landmasses. The least radiogenic seawater ɛHf signatures (up to -11.7) are found in surface waters close to Greenland and near the Canadian margin. This reflects the influence of recirculating Irminger Current Waters, which are affected by highly unradiogenic inputs from Greenland. A three to four ɛHf unit difference is observed between Denmark Strait Overflow Water (ɛHf ∼ -4) and North East Atlantic Deep Water (ɛHf ∼ -0

  15. Tungsten isotopic compositions in stardust SiC grains from the Murchison meteorite: Constraints on the s-process in the Hf-Ta-W-Re-Os region

    CERN Document Server

    Ávila, J N; Ireland, T R; Gyngard, F; Zinner, E; Cristallo, S; Holden, P; Buntain, J; Amari, S; Karakas, A


    We report the first tungsten isotopic measurements in stardust silicon carbide (SiC) grains recovered from the Murchison carbonaceous chondrite. The isotopes 182W, 183W, 184W, 186W and 179Hf, 180Hf were measured on both an aggregate (KJB fraction) and single stardust SiC grains (LS+LU fraction) believed to have condensed in the outflows of low-mass carbon-rich asymptotic giant branch (AGB) stars with close-to-solar metallicity. The SiC aggregate shows small deviations from terrestrial (=solar) composition in the 182W/184W and 183W/184W ratios, with deficits in 182W and 183W with respect to 184W. The 186W/184W ratio, however, shows no apparent deviation from the solar value. Tungsten isotopic measurements in single mainstream stardust SiC grains revealed lower than solar 182W/184W, 183W/184W, and 186W/184W ratios. We have compared the SiC data with theoretical predictions of the evolution of W isotopic ratios in the envelopes of AGB stars. These ratios are affected by the slow neutron-capture process and match...

  16. Assessing the isotopic evolution of S-type granites of the Carlos Chagas Batholith, SE Brazil: Clues from U-Pb, Hf isotopes, Ti geothermometry and trace element composition of zircon (United States)

    Melo, Marilane G.; Lana, Cristiano; Stevens, Gary; Pedrosa-Soares, Antônio C.; Gerdes, Axel; Alkmin, Leonardo A.; Nalini, Hermínio A.; Alkmim, Fernando F.


    The Carlos Chagas batholith (CCB) is a very large ( 14,000 km2) S-type granitic body formed during the syn-collisional stage of the Araçuaí orogen (southeastern Brazil). Zircons extracted from the CCB record a wide range of U-Pb ages (from 825 to 490 Ma), indicating a complex history of inheritance, magmatic crystallization and partial melting during the evolution of the orogeny. Magmatic zircons (ca. 578-588 Ma) are marked by similar Hf isotope compositions and REE patterns to those of inherited cores (ca. 825-600 Ma), indicating that these aspects of the chemical signature of the magmatic zircons have likely been inherited from the source. The U-Pb ages and initial 176Hf/177Hf ratios from anatectic and metamorphic zircon domains are consistent with a two-stage metamorphic evolution marked by contrasting mechanisms of zircon growth and recrystallization during the orogeny. Ti-in-zircon thermometry is consistent with the findings of previous metamorphic work and indicates that the two metamorphic events in the batholith reached granulite facies conditions (> 800 °C) producing two generations of garnet via fluid-absent partial melting reactions. The oldest metamorphic episode (ca. 570-550 Ma) is recorded by development of thin anatectic overgrowths on older cores and by growth of new anatectic zircon crystals. Both domains have higher initial 176Hf/177Hf values compared to relict cores and display REE patterns typical of zircon that grew contemporaneously with peritectic garnet through biotite-absent fluid partial melting reactions. Hf isotopic and chemical evidences indicate that a second anatectic episode (ca. 535-500 Ma) is only recorded in parts from the CCB. In these rocks, the growth of new anatectic zircon and/or overgrowths is marked by high initial 176Hf/177Hf values and also by formation of second generation of garnet, as indicated by petrographic observations and REE patterns. In addition, some rocks contain zircon crystals formed by solid

  17. Stages of late Paleozoic to early Mesozoic magmatism in the Song Ma belt, NW Vietnam: evidence from zircon U-Pb geochronology and Hf isotope composition (United States)

    Hieu, Pham Trung; Li, Shuang-Qing; Yu, Yang; Thanh, Ngo Xuan; Dung, Le Tien; Tu, Vu Le; Siebel, Wolfgang; Chen, Fukun


    The Song Ma zone in NW Vietnam bears important tectonic implications as a potential subduction corridor between the Indochina and South China blocks. On the basis of U-Pb ages, the Hf isotopic characteristics of zircons and the geochemical composition of granitoids, a two-stage magmatic evolution process of the Song Ma zone at ~290-260 and ~245-230 Ma can be proposed. Isotopic analyses indicate magmatic contributions from Neoproterozoic oceanic island basalt, Proterozoic continental crust, and depleted mantle or juvenile lithosphere. By combining geochronological and geochemical data from the granitoid rocks, we suggest that the staged magmatic processes of Song Ma zone may be related to a long-lasting period of ocean subduction (ca. 290-260 Ma) and subsequent syn-/post-collisional evolution (ca. 245-230 Ma).


    Energy Technology Data Exchange (ETDEWEB)

    Avila, Janaina N.; Ireland, Trevor R.; Holden, Peter [Research School of Earth Sciences, Australian National University, Canberra, ACT 0200 (Australia); Lugaro, Maria; Buntain, Joelene [Centre for Stellar and Planetary Astrophysics, Monash University, Clayton, VIC 3800 (Australia); Gyngard, Frank; Zinner, Ernst; Amari, Sachiko [Laboratory for Space Sciences and the Department of Physics, Washington University, One Brookings Drive, St. Louis, MO 63130 (United States); Cristallo, Sergio [Departamento de Fisica Teorica y del Cosmos, Universidad de Granada, Granada 18071 (Spain); Karakas, Amanda, E-mail: [Mount Stromlo Observatory, Australian National University, Weston Creek, ACT 2611 (Australia)


    We report the first tungsten isotopic measurements in stardust silicon carbide (SiC) grains recovered from the Murchison carbonaceous chondrite. The isotopes {sup 182,183,184,186}W and {sup 179,180}Hf were measured on both an aggregate (KJB fraction) and single stardust SiC grains (LS+LU fraction) believed to have condensed in the outflows of low-mass carbon-rich asymptotic giant branch (AGB) stars with close-to-solar metallicity. The SiC aggregate shows small deviations from terrestrial (= solar) composition in the {sup 182}W/{sup 184}W and {sup 183}W/{sup 184}W ratios, with deficits in {sup 182}W and {sup 183}W with respect to {sup 184}W. The {sup 186}W/{sup 184}W ratio, however, shows no apparent deviation from the solar value. Tungsten isotopic measurements in single mainstream stardust SiC grains revealed lower than solar {sup 182}W/{sup 184}W, {sup 183}W/{sup 184}W, and {sup 186}W/{sup 184}W ratios. We have compared the SiC data with theoretical predictions of the evolution of W isotopic ratios in the envelopes of AGB stars. These ratios are affected by the slow neutron-capture process and match the SiC data regarding their {sup 182}W/{sup 184}W, {sup 183}W/{sup 184}W, and {sup 179}Hf/{sup 180}Hf isotopic compositions, although a small adjustment in the s-process production of {sup 183}W is needed in order to have a better agreement between the SiC data and model predictions. The models cannot explain the {sup 186}W/{sup 184}W ratios observed in the SiC grains, even when the current {sup 185}W neutron-capture cross section is increased by a factor of two. Further study is required to better assess how model uncertainties (e.g., the formation of the {sup 13}C neutron source, the mass-loss law, the modeling of the third dredge-up, and the efficiency of the {sup 22}Ne neutron source) may affect current s-process predictions.

  19. Zircon and baddeleyite from the economic ultramafic-mafic Noril'sk-1 intrusion (Russia): Hf-isotope constraints on source composition (United States)

    Malitch, K. N.; Belousova, E. A.; Badanina, I. Yu.; Griffin, W. L.


    of the Noril'sk-1 intrusion, which served as the favorable factor for accumulation of ores of unique scales and concentrations, To test this hypothesis, in situ Hf-isotope data were collected on the dated spots within single zircon grains. The analysis used a New Wave LUV213 laser-ablation microprobe attached to a Nu plasma MC-ICP-MS at GEMOC (Griffin et al. 2002). Hf-isotope results grouped on the basis of lithology show notable differences. Zircons from the unmineralized 'layered rock sequence' (e.g., olivine-free gabbro, olivine-bearing gabbro and olivine gabbro) are characterized by the most 'radiogenic' initial 176Hf/177Hf and some of ɛHf values close to those of the Depleted Mantle. Irrespective of zircon population most radiogenic Hf-isotope compositions are typical for olivine-free gabbro (mean ɛHf 7.3 ± 1.1 for sample N1-4), olivine-bearing gabbro (9.2 ± 3.8, sample N1-5) and olivine gabbro (8.3 ± 2.0, sample N1-6). In contrast, zircons from the leucogabbro that encloses the low-sulphide horizon (N1-3), and plagiowehrlite (N1-7) and taxitic-textured rocks (N1-8 and N1-9) with disseminated sulphide ores have less radiogenic Hf-isotope values (e.g., mean ɛHf6.2 ± 1.4, 5.9 ± 2.3, 6.4 ± 1.2 and 4.9±1.4, respectively). The least radiogenic values (ɛHffrom -2.9 to +2.3, mean ɛHf = 0.1 ± 1.9) are recorded in gabbro-diorite from the upper part of intrusion. The baddeleyite from olivine-free gabbro has the narrowest range of ɛHf values (e.g. 6.8-8.4), with a mean of ɛHfof 7.6 ± 0.8, closely matching that of zircon (mean ɛHf= 7.3 ± 1.1). Zircons from the leucogabbro that hosts the low-sulphide horizon (N1-3), and ultramafic and taxitic-textured lithologies with disseminated sulphide ores (N1-7, N1-8 and N1-9) have less radiogenic ɛHf values than those in barren lithologies. The Hf-isotope data for zircons from ore-bearing rocks thus suggest that the Noril'sk magmas represent mixing between a juvenile source equivalent to the Depleted Mantle and a

  20. Systematic Study on Triaxial Superdeformed Bands of Hf Isotopes

    Institute of Scientific and Technical Information of China (English)

    ZHANG Da-Li; DING Bin-Gang


    Properties of the triaxial superdeformed (TSD) bands of Hf isotopes are investigated systematically within the supersymmetry scheme including many-body interactions and a perturbation possessing the SO(5) (or SU(5)) symmetry on the rotational symmetry. Quantitatively good results of the γ-ray energies, the dynamical moments of inertia,and the spin of the TSD bands in Hf isotopes are obtained. It shows that this approach is quite powerful in describing the properties of the triaxial superdeformation in Hf isotopes.

  1. What Hf isotopes in zircon tell us about crust-mantle evolution (United States)

    Iizuka, Tsuyoshi; Yamaguchi, Takao; Itano, Keita; Hibiya, Yuki; Suzuki, Kazue


    The 176Lu-176Hf radioactive decay system has been widely used to study planetary crust-mantle differentiation. Of considerable utility in this regard is zircon, a resistant mineral that can be precisely dated by the U-Pb chronometer and record its initial Hf isotope composition due to having low Lu/Hf. Here we review zircon U-Pb age and Hf isotopic data mainly obtained over the last two decades and discuss their contributions to our current understanding of crust-mantle evolution, with emphasis on the Lu-Hf isotope composition of the bulk silicate Earth (BSE), early differentiation of the silicate Earth, and the evolution of the continental crust over geologic history. Meteorite zircon encapsulates the most primitive Hf isotope composition of our solar system, which was used to identify chondritic meteorites best representative of the BSE (176Hf/177Hf = 0.282793 ± 0.000011; 176Lu/177Hf = 0.0338 ± 0.0001). Hadean-Eoarchean detrital zircons yield highly unradiogenic Hf isotope compositions relative to the BSE, providing evidence for the development of a geochemically enriched silicate reservoir as early as 4.5 Ga. By combining the Hf and O isotope systematics, we propose that the early enriched silicate reservoir has resided at depth within the Earth rather than near the surface and may represent a fractionated residuum of a magma ocean underlying the proto-crust, like urKREEP beneath the anorthositic crust on the Moon. Detrital zircons from world major rivers potentially provide the most robust Hf isotope record of the preserved granitoid crust on a continental scale, whereas mafic rocks with various emplacement ages offer an opportunity to trace the Hf isotope evolution of juvenile continental crust (from εHf[4.5 Ga] = 0 to εHf[present] = + 13). The river zircon data as compared to the juvenile crust composition highlight that the supercontinent cycle has controlled the evolution of the continental crust by regulating the rates of crustal generation and intra

  2. Petrogenesis of gold-mineralized magmatic rocks of the Taerbieke area, northwestern Tianshan (western China): Constraints from geochronology, geochemistry and Sr-Nd-Pb-Hf isotopic compositions (United States)

    Tang, Gong-Jian; Wang, Qiang; Wyman, Derek A.; Sun, Min; Zhao, Zhen-Hua; Jiang, Zi-Qi


    Many Late Paleozoic Cu-Au-Mo deposits occur in the Central Asian Orogenic Belt (CAOB). However, their tectonic settings and associated geodynamic processes have been disputed. This study provides age, petrologic and geochemical data for andesites and granitic porphyries of the Taerbieke gold deposit from the Tulasu Basin, in the northwestern Tianshan Orogenic Belt (western China). LA-ICP-MS zircon U-Pb dating indicates that the granitic porphyries have an Early Carboniferous crystallization age (349 ± 2 Ma) that is broadly contemporaneous with the eruption age (347 ± 2 Ma) of the andesites. The andesites have a restricted range of SiO2 (58.94-63.85 wt.%) contents, but relatively high Al2O3 (15.39-16.65 wt.%) and MgO (2.51-6.59 wt.%) contents, coupled with high Mg# (57-69) values. Geochemically, they are comparable to Cenozoic sanukites in the Setouchi Volcanic Belt, SW Japan. Compared with the andesites, the granitic porphyries have relatively high SiO2 (72.68-75.32 wt.%) contents, but lower Al2O3 (12.94-13.84 wt.%) and MgO (0.10-0.33 wt.%) contents, coupled with lower Mg# (9-21) values. The andesites and granitic porphyries are enriched in both large ion lithophile and light rare earth elements, but depleted in high field strength elements, similar to those of typical arc magmatic rocks. They also have similar Nd-Hf-Pb isotope compositions: ɛNd(t) (+0.48 to +4.06 and -0.27 to +2.97) and zircons ɛHf(t) (+3.4 to +8.0 and -1.7 to +8.2) values and high (206Pb/204Pb)i (18.066-18.158 and 17.998-18.055). We suggest that the Taerbieke high-Mg andesitic magmas were generated by the interaction between mantle wedge peridotites and subducted oceanic sediment-derived melts with minor basaltic oceanic crust-derived melts, and that the magmas then fractionated to produce the more felsic members (i.e., the Taerbieke granitic porphyries) during late-stage evolution. Taking into account the Carboniferous magmatic record from the western Tianshan Orogenic Belt, we suggest that

  3. Hf-Nd isotope and trace element constraints on subduction inputs at island arcs: Limitations of Hf anomalies as sediment input indicators (United States)

    Handley, Heather K.; Turner, Simon; Macpherson, Colin G.; Gertisser, Ralf; Davidson, Jon P.


    New Nd-Hf isotope and trace element data for Javanese volcanoes are combined with recently published data to place constraints on subduction inputs at the Sunda arc in Indonesia and assess the value of Hf anomalies (expressed as Hf/Hf* and Sm/Hf ratios) as tracers of such inputs. Hf anomaly does not correlate with Hf isotope ratio in Javanese lavas, however, Hf/Hf* and Sm/Hf ratios do correlate with SiO 2. Contrary to previous work, we show that Hf anomaly variation may be controlled by fractionation of clinopyroxene and/or amphibole during magmatic differentiation and does not represent the magnitude or type of subduction input in some arcs. Correlation of Sm/Hf with indices of differentiation for other arcs (e.g., Vanuatu, New Britain, and Mariana) suggests that differentiation control on Sm/Hf ratios in volcanic arc rocks may be a relatively common phenomenon. This study corroborates the use of Nd-Hf isotope co-variations in arc volcanic rocks to ascertain subduction input characteristics. The trajectories of regional volcano groups (East, Central and West Java) in Nd-Hf isotope space reveal heterogeneity in the subducted sediment input along Java, which reflects present-day spatial variations in sediment compositions on the down-going plate in the Java Trench. The high Sm/Hf ratio required in the sediment end-member for some Javanese basalts suggests that partial melting of subducted sediment occurs in the presence of residual zircon, and is inconsistent with residual monazite or allanite.

  4. Probing Archean lithosphere using the Lu-Hf isotope systematics of peridotite xenoliths from Somerset Island kimberlites, Canada (United States)

    Schmidberger, Stefanie S.; Simonetti, Antonio; Francis, Don; Gariépy, Clément


    A knowledge of the Hf isotopic composition of the subcontinental lithosphere beneath Archean cratons is essential to constrain the Hf isotope budget of the Earth's mantle. Hf isotopic measurements were obtained by MC-ICP-MS for a suite of refractory peridotite xenoliths and constituent garnets from the Nikos kimberlite (100 Ma) on Somerset Island in order to constrain the isotopic composition and age of the lithosphere beneath the northern Canadian craton. The low-temperature Nikos peridotites (Somerset lithosphere, are characterized by higher 176Lu/ 177Hf ratios (0.03-0.05) and Hf isotopic values ( 176Hf/ 177Hf (0.1Ga)=0.28296-0.28419) than the deep-seated high-temperature peridotites (>1100°C; 0.004-0.03, 0.28265-0.28333, respectively). These differences in Hf isotope signatures suggest that shallow and deep subcontinental lithosphere beneath Somerset Island represent isotopically distinct domains and do not share a common petrogenetic history. The Lu-Hf isotope systematics of the shallow low-temperature peridotites define a positively sloped line that plot along a 2.8 Ga reference isochron. A number of these peridotites are characterized by highly radiogenic Hf isotopic compositions suggestive of long-term radiogenic ingrowth (billions of years). These findings are consistent with an interpretation that the shallow Somerset lithosphere (to depths of ˜150 km) stabilized in the Archean. The majority of the high-temperature peridotites plot closer to the composition of the host kimberlite. Although the observed isotopic variation may be attributed in part to kimberlite-related Hf addition, it is possible that these deep-seated xenoliths represent younger mantle. The superchondritic 176Lu/ 177Hf ratios observed for a number of the shallow low-temperature peridotites indicate strong fractionation of Lu and Hf, suggesting mantle root formation in the garnet stability field (depths >80 km). The Hf isotope compositions for the Somerset low-temperature peridotites

  5. Garnet effect on Nd-Hf isotope decoupling: Evidence from the Jinfosi batholith, Northern Tibetan Plateau (United States)

    Huang, Hui; Niu, Yaoling; Mo, Xuanxue


    The initial Nd and Hf isotope ratios of a 420 Ma post-collisional dioritic-granitic batholith from the Northern Tibetan plateau define a negative trend above and orthogonal to the ԐHf(t)-ԐNd(t) terrestrial array. This uncommon trend offers an insight into the origin of the puzzling Nd-Hf isotope decoupling in the crustal rocks. On this trend, samples depleted in heavy rare earth elements (HREEs, i.e., [Dy/Yb]N ≫ 1) deviate most from the terrestrial array whereas samples with flat HREEs (i.e., [Dy/Yb]N ≥ 1) deviate less or plot within the terrestrial array, pointing to the controlling effect of garnet in the magma source. Ancient garnet-bearing residues after melt extraction will have elevated Lu/Hf ratios and can evolve with time to produce high ԐHf(t) at a low ԐNd(t) value. Mixing of melts derived from such source lithologies (high Lu/Hf) with melts possessing a within-terrestrial array Nd-Hf isotopic composition (low Lu/Hf) best explains the observed trend orthogonal to the terrestrial array. The samples from the Jinfosi batholith with the most decoupled Nd-Hf isotope compositions require a larger degree (> 40%) and ancient (i.e., ≥ 1.8 Gyr) previous melt extraction from their source. It follows that the ancient melts with depleted HREEs complementary to those garnet-bearing residues should have low ԐHf values and plot below the terrestrial array, which is indeed shown by some Archean/Paleoproterozic TTGs.

  6. Subduction Controls of Hf and Nd Isotopes in Lavas of the Aleutian Island Arc

    Energy Technology Data Exchange (ETDEWEB)

    Yogodzinski, Gene; Vervoort, Jeffery; Brown, Shaun Tyler; Gerseny, Megan


    The Hf and Nd isotopic compositions of 71 Quaternary lavas collected from locations along the full length of the Aleutian island arc are used to constrain the sources of Aleutian magmas and to provide insight into the geochemical behavior of Nd and Hf and related elements in the Aleutian subduction-magmatic system. Isotopic compositions of Aleutian lavas fall approximately at the center of, and form a trend parallel to, the terrestrial Hf-Nd isotopic array with {var_epsilon}{sub Hf} of +12.0 to +15.5 and {var_epsilon}{sub Nd} of +6.5 to +10.5. Basalts, andesites, and dacites within volcanic centers or in nearby volcanoes generally all have similar isotopic compositions, indicating that there is little measurable effect of crustal or other lithospheric assimilation within the volcanic plumbing systems of Aleutian volcanoes. Hafnium isotopic compositions have a clear pattern of along-arc increase that is continuous from the eastern-most locations near Cold Bay to Piip Seamount in the western-most part of the arc. This pattern is interpreted to reflect a westward decrease in the subducted sediment component present in Aleutian lavas, reflecting progressively lower rates of subduction westward as well as decreasing availability of trench sediment. Binary bulk mixing models (sediment + peridotite) demonstrate that 1-2% of the Hf in Aleutian lavas is derived from subducted sediment, indicating that Hf is mobilized out of the subducted sediment with an efficiency that is similar to that of Sr, Pb and Nd. Low published solubility for Hf and Nd in aqueous subduction fluids lead us to conclude that these elements are mobilized out of the subducted component and transferred to the mantle wedge as bulk sediment or as a silicate melt. Neodymium isotopes also generally increase from east to west, but the pattern is absent in the eastern third of the arc, where the sediment flux is high and increases from east to west, due to the presence of abundant terrigenous sediment in the

  7. U-Pb zircon dating, geochemical and Sr-Nd-Hf isotopic compositions of mafic intrusive rocks in the Motuo, SE Tibet constrain on their petrogenesis and tectonic implication (United States)

    Pan, Fa-Bin; Zhang, Hong-Fei; Xu, Wang-Chun; Guo, Liang; Luo, Bi-Ji; Wang, Shuai


    Mafic intrusive rocks are widely exposed in the Motuo tectono-magmatic belt, southeast Lhasa terrane. LA-ICP-MS U-Pb zircon dating shows that they have magma crystallization ages of 69 and ca. 50 Ma. These mafic intrusive rocks are characterized by variable SiO2 (44.60-57.60 wt.%), high Al2O3 (17.19-20.86 wt.%), and low MgO (1.85-5.38 wt.%) with Mg# of 31-55. Their chemical composition is comparable with low-MgO high-Al basalts to basaltic andesites. They are enriched in LILEs (Rb, Ba, K) and LREE and depleted in HFSEs (Nb, Ta, Zr, Hf, Ti), with weakly evolved Sr-Nd-Hf compositions (whole-rock (87Sr/86Sr)0 = 0.7064 to 0.7086, εNd(t) = - 3.41 to + 1.22, and zircon εHf(t) = - 3.8 to + 6.4). The mafic rocks were derived from partial melting of metasomatized lithospheric mantle. Geochemical and Sr-Nd-Hf isotopic data show that they were insignificantly modified during magma emplacement. We provide a different secular evolution of the lithospheric mantle beneath the eastern part relative to the central part of the southern Lhasa terrane. Sr-Nd isotopic composition of the Motuo Late Cretaceous-Eocene mafic rocks argues that they were derived from partial melting of a relatively homogeneous and depleted lithospheric mantle. We propose that the Late Cretaceous delamination resulted in the replacement of ancient lithospheric mantle by the juvenile homogeneous lithospheric mantle in the eastern Lhasa terrane. The foundered ancient materials may subsequently re-fertilize the lithospheric mantle not only in the eastern Lhasa terrane but also in the surrounding areas.

  8. Tracing Proterozoic arc mantle Hf isotope depletion of southern Fennoscandia through coupled zircon U-Pb and Lu-Hf isotopes (United States)

    Petersson, Andreas; Bjärnborg, Karolina; Scherstén, Anders; Gerdes, Axel; Næraa, Tomas


    Constraints on the composition of the depleted mantle Sm-Nd and Lu-Hf crust formation ages have a long history of scientific debate. When calculating mantle extraction ages, and constructing crustal growth models, a linear evolution of incompatible trace elements in a depleted mantle since > 4 Ga is routinely used. Mantle depletion however varies regionally and over time and subduction of sediments and oceanic crust renders a mantle-wedge variously enriched relative to a modelled depleted mantle. Here we show that primitive mantle-derived subduction related gabbroic intrusions from southern Fennoscandia have Hf isotope compositions that are enriched relative to a MORB-like linear depleted mantle evolution curve. Extrapolation of primitive Paleoproterozoic gabbro suites enables the construction of a regional mantle evolution curve, providing improved constraints on model ages, crustal residence times and the fraction of juvenile versus reworked continental crust. Convergent margins are assumed to be one of the main sites of continental crust growth, and using an overly depleted mantle source yield model ages that are too old, and hence cumulative crustal growth models show too much crust generation early in the Earth's history. The approach of using the Hf isotope composition of zircon from primitive subduction related gabbroic intrusions as a proxy for mantle Hf isotope composition, piloted in this study, can be applied to other convergent margins.

  9. Distribution of p-process 174Hf in early solar system materials and the origin of nucleosynthetic Hf and W isotope anomalies in Ca-Al rich inclusions (United States)

    Peters, Stefan T. M.; Münker, Carsten; Pfeifer, Markus; Elfers, Bo-Magnus; Sprung, Peter


    Some nuclides that were produced in supernovae are heterogeneously distributed between different meteoritic materials. In some cases these heterogeneities have been interpreted as the result of interaction between ejecta from a nearby supernova and the nascent solar system. Particularly in the case of the oldest objects that formed in the solar system - Ca-Al rich inclusions (CAIs) - this view is confirm the hypothesis that a nearby supernova event facilitated or even triggered solar system formation. We present Hf isotope data for bulk meteorites, terrestrial materials and CAIs, for the first time including the low-abundance isotope 174Hf (∼0.16%). This rare isotope was likely produced during explosive O/Ne shell burning in massive stars (i.e., the classical "p-process"), and therefore its abundance potentially provides a sensitive tracer for putative heterogeneities within the solar system that were introduced by supernova ejecta. For CAIs and one LL chondrite, also complementary W isotope data are reported for the same sample cuts. Once corrected for small neutron capture effects, different chondrite groups, eucrites, a silicate inclusion of a IAB iron meteorite, and terrestrial materials display homogeneous Hf isotope compositions including 174Hf. Hafnium-174 was thus uniformly distributed in the inner solar system when planetesimals formed at the system composition, and also variable r-process (or s-process) Hf and W contributions. Based on combined Hf and W isotope compositions, we show that CAIs sampled at least one component in which the proportion of r- and s-process derived Hf and W deviates from that of supernova ejecta. The Hf and W isotope anomalies in CAIs are therefore best explained by selective processing of presolar carrier phases prior to CAI formation, and not by a late injection of supernova materials. Likewise, other isotope anomalies in additional elements in CAIs relative to the bulk solar system may reflect the same process. The isotopic

  10. Persistence of fertile and hydrous lithospheric mantle beneath the northwestern Ethiopian plateau: Evidence from modal, trace element and Sr-Nd-Hf isotopic compositions of amphibole-bearing mantle xenoliths (United States)

    Alemayehu, Melesse; Zhang, Hong-Fu; Aulbach, Sonja


    We present new trace element compositions of amphiboles, Sr-Nd-Hf isotope compositions of clinopyroxenes and mineral modes for spinel peridotite xenoliths that were entrained in a Miocene alkali basalt (Gundeweyn, northwestern Ethiopian plateau), in order to understand the geochemical evolution and variation occurring within the continental lithospheric mantle (CLM) in close proximity to the East African Rift system, and its dynamic implications. With the exception of a single amphibole-bearing sample that is depleted in LREE (La/YbN = 0.45 × Cl), amphiboles in lherzolites and in one harzburgite show variable degrees of LREE enrichment (La/YbN = 2.5-12.1 × Cl) with flat HREE (Dy/YbN = 1.5-2.1 × Cl). Lherzolitic clinoyroxenes have 87Sr/86Sr (0.70227 to 0.70357), 143Nd/144Nd (0.51285 to 0.51346), and 176Hf/177Hf (0.28297 to 0.28360) ranging between depleted lithosphere and enriched mantle. LREE-enriched clinopyroxenes generally have more enriched isotope compositions than depleted ones. While lherzolites with isotope compositions similar to those of the Afar plume result from the most recent metasomatic overprint, isotope compositions more depleted than present-day MORB can be explained by an older melt extraction and/or isotopic rehomogenisation event, possibly related to the Pan-African orogeny. Several generations of amphibole are recognized in accord with this multi-stage evolution. Texturally unequilibrated amphibole occurring within the peridotite matrix and in melt pockets attest to continued hydration and refertilization of the lithospheric mantle subsequent to Oligocene flood basalt magmatism, during which an earlier-emplaced inventory of amphibole was likely largely consumed. However, a single harzburgite contains amphibole with the highest Mg# and lowest TiO2 content, which is interpreted as sampling a volumetrically subordinate mantle region beneath the Ethiopian plateau that was not tapped during flood basalt magmatism. Strikingly, both trace

  11. Serpentinization Changes Nd, but not Hf Isotopes of Abyssal Peridotites (United States)

    Bizimis, M.; Frisby, C. P.; Mallick, S.


    Serpentinization of the oceanic lithosphere is a known sink for fluid mobile elements (B, Cl, Li, Sr, etc.), while high field strength elements (HFSE: e.g., Hf, Zr, Ti, Nb) are thought to be unaffected by it. In contrast, the fate of REE during serpentinization is equivocal. Correlations between REE and HFSE concentrations in abyssal peridotites suggest control by magmatic processes (Niu, 2004, J. Pet), while some LREE enrichments in serpentinized peridotites compared to their clinopyroxene (cpx) and Nd, Sr isotope data (Delacour et al., 2008, Chem. Geol.) imply seawater-derived REE addition to the mantle protolith (Paulick et al., 2006, Chem. Geol). To further constrain peridotite-seawater interaction during serpentinization we compare bulk rock and cpx Hf and Nd isotope data in partially (up to ~70%) serpentinized abyssal peridotites (9-16°E South West Indian Ridge). We also present a new method that improves yields in Hf, Nd and Pb separations from depleted (90% of Hf, Zr, Ti are retained in the residue. LA-ICPMS data shows that serpentine after olivine typically has higher LREE/HREE ratios than cpx, pronounced negative Ce anomalies, high U, Sr concentrations and low HFSE, unlike the coexisting cpx. These data are consistent with some seawater-derived LREE addition to peridotite during serpentinization, localized in the serpentine and other secondary phases, while cpx retains the magmatic value. This process will lower the Sm/Nd relative to Lu/Hf ratio in the peridotite and can lead to decoupled radiogenic Hf and unradiogenic Nd isotopes upon recycling and aging. Our data further testifies to the fidelity of Hf isotopes in tracing mantle processes, even in serpentinized rocks.

  12. Zircon U-Pb Geochronology, Hf Isotopic Composition and Geological Implications of the Neoproterozoic Huashan Group in the Jingshan Area, Northern Yangtze Block, China (United States)

    Yang, Z.; Yang, K.


    In the northern Yangtze Block, a clear angular unconformity between the Mesoproterozoic sequences (e.g. Dagushi Group) and the overlying Neoproterozoic strata (e.g. Huashan Group) marks the the Jinning orogeny. A combined study of Lu-Hf isotopes and U-Pb ages for detrital zircons from Huashan Group can provide information on the crustal evolution of sedimentary provenances and the timing of the Jinning orogeny. Detrital zircons from Huashan Group have two major U-Pb age populations of about 2.0Ga, 2.65Ga, and three subordinate age groups of about 0.82Ga, 2.5Ga, 2.9Ga with minor >3.0Ga ages. The youngest five analyses yield a weighted average age of 816±9Ma, which is consistent with that of interlayered basalt (824±9Ma, Deng et al., 2013) and roughly defines the minimum depositional age of Huashan Group. Detrital zircons of Huashan Group mostly have two stage Hf isotope model ages (TDM2) between 3.0 to 3.3Ga, indicating that the northern Yangtze Block experienced significant continental crustal growth during the Paleo- to Meso-archean. Similar U-Pb ages of detrital zircons have been obtained from Precambrian sedimentary rocks in the northern Yangtze Block from previous studies (Liu et al., 2008; Guo et al., 2014 and references therein). Recently, ca. 2.65Ga A-type granites had been reported from the Kongling and Huji area, which likely record the thermally stable lithosphere (Chen et al., 2013; Zhou et al., 2015). In combination with this study, it documents the widespread 2.6-2.7Ga magmatic rocks in the northern Yangtze Block. Zhao et al. (2013) demonstrated both the ca. 850Ma tonalite and trondhjemite of the Huangling igneous complex were formed in a continental arc setting. This suggests the Miaowan-Huashan oceanic basin proposed by Bader et al. (2013) has not been closed at ca. 850Ma. This evidence, together with the depositional age of the Huashan Group, indicates the Jinning orogeny took place at 850-820 Ma. [1] Bader et al., 2013 Tectonics [2] Deng et al

  13. Archean Lithosphere Beneath Arctic Canada: Lu-Hf Isotope Systematics for Kimberlite-Hosted Garnet-Peridotites From Somerset Island (United States)

    Schmidberger, S. S.; Simonetti, A.; Francis, D.; Gariepy, C.


    Knowledge of the age of lithospheric mantle underlying the continents provides valuable constraints for the timing of formation and stabilization of Archean cratons. This study reports Lu-Hf isotopic data for garnet-peridotites, and their constituent garnets, from the Nikos kimberlite (100 Ma) on Somerset Island in the Canadian Arctic obtained using a Micromass IsoProbe multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS) at GEOTOP-UQAM. The low temperature peridotites (1100 C; 160-190 km) and their 176Hf/177Hf(0.1Ga) isotopic compositions (0.28265-0.28333; \\epsilonHf(0.1Ga)=-2 to +22) are less radiogenic than those of the shallow xenoliths. A Lu-Hf isochron for six peridotites yields a mid Archean age of 3.4\\pm0.3 Ga and an initial 176Hf/177Hf ratio of 0.28101\\pm24. The remaining peridotites (n=9), in contrast, are characterized by extremely high (+35) initial \\epsilonHf(3.4Ga) values, which correlate negatively with their 176Lu/177Hf ratios, suggesting addition of Hf as a result of metasomatic interaction with the host kimberlite. The garnets from the low temperature (3.4 Ga old) peridotites are characterized by high 176Lu/177Hf ratios and define an errorchron age of 1.4\\pm0.2 Ga, which may reflect re-equilibration of Hf during kimberlite magmatism.

  14. Mixing and melt sources in the Miocene Aztec Wash pluton (Nevada, USA) as revealed by zircon Hf and O and whole rock Sr, Nd, and Hf isotopes (United States)

    Ryan, M.; Miller, J. S.; Miller, C. F.; Bromley, S.; Davies, G. R.; Schmitt, A. K.


    The 15.6 Ma Aztec Wash Pluton (AWP) is one of several Miocene intrusions located within the northern Colorado River extensional corridor. Extensive E-W tilting of fault blocks has exposed the pluton from the roof to 5 km structural depth. Earlier field and petrologic studies subdivided the AWP into two distinct zones: (1) a Granite Zone (GZ) comprised of relatively homogeneous granite with subtle differences in textures and mineralogy; (2) a Heterogeneous Zone (HZ), which interfingers the GZ, contains evidence for mafic and felsic magma input with a wide compositional range (42-78 wt% SiO2), and abundant field evidence for hybridization. Previous whole rock geochemistry and zircon trace element analyses indicated that compositional variation was produced by multi-component mixing between mafic and felsic melts within the HZ. New whole rock Sr, Nd, and Hf isotope data from the HZ show that all rocks (including high-silica granites) formed by mixing Precambrian crust and enriched mantle, with mixtures having a large mantle fraction (≥50%). New Hf (n=189) and O (n=241) isotope analyses of zircon from samples in the HZ confirm these melt sources and provide a broader perspective on hybridization processes within the AWP. Zircon grains from all samples show heterogeneous Hf and O isotopic compositions (-5 to -18 ɛHf; 4.5-7.5% δ18O), but despite the clear signature of Precambrian crust in the whole rock data, obvious Precambrian zircons (or cores) were mostly absent; only one zircon was clearly Precambrian (ɛHf = -25). Resolvable intragrain variability is relatively limited (including the Precambrian grain, which is unzoned). Zircons from hand samples and from compositional groups also show heterogeneous ɛHf and δ18O values, although the spreads are more restricted than in the whole data set (6-10 ɛHf in granites, 5-7 ɛHf in intermediate "hybrids", 5-6 ɛHf in gabbro/diorite sheets). Oxygen isotope values for the zircons also show intra-handsample heterogeneity

  15. Hf isotope evidence for a hidden mantle reservoir

    DEFF Research Database (Denmark)

    Bizzarro, Martin; Simonetti, A.; Stevenson, R.K.


    High-precision Hf isotopic analyses and U-Pb ages of carbonatites and kimberlites from Greenland and eastern North America, including Earth's oldest known carbonatite (3 Ga), indicate derivation from an enriched mantle source. This previously unidentified mantle reservoir-marked by an unradiogeni...

  16. Tectono-magmatic evolution of the Chihuahua-Sinaloa border region in northern Mexico: Insights from zircon-apatite U-Pb geochronology, zircon Hf isotope composition and geochemistry of granodiorite intrusions (United States)

    Mahar, Munazzam Ali; Goodell, Philip C.; Feinstein, Michael Nicholas


    We present the whole-rock geochemistry, LA-ICP-MS zircon-apatite U-Pb ages and zircon Hf isotope composition of the granodioritic plutons at the southwestern boundary of Chihuahua with the states of Sinaloa and Sonora. These granodiorites are exposed in the north and south of the Rio El Fuerte in southwest Chihuahua and northern Sinaloa. The magmatism spans over a time period of 37 Ma from 90 to 53 Ma. Zircons are exclusively magmatic with strong oscillatory zoning. No inheritance of any age has been observed. Our new U-Pb dating ( 250 analyses) does not support the involvement of older basement lithologies in the generation of the granitic magmas. The U-Pb apatite ages from granodiorites in southwest Chihuahua vary from 52 to 70 Ma. These apatite ages are 1 to 20 Ma younger than the corresponding zircon U-Pb crystallization ages, suggesting variable cooling rates from very fast to 15 °C/Ma ( 800 °C to 500 °C) and shallow to moderate emplacement depths. In contrast, U-Pb apatite ages from the Sinaloa batholith are restricted from 64 to 61 Ma and are indistinguishable from the zircon U-Pb ages range from 67 to 60 Ma within the error, indicating rapid cooling and very shallow emplacement. However, one sample from El Realito showed a larger difference of 20 Ma in zircon-apatite age pair: zircon 80 ± 0.8 Ma and apatite 60.6 ± 4 Ma, suggesting a slower cooling rate of 15 °C/Ma. The weighted mean initial εHf (t) isotope composition (2σ) of granodiorites varies from + 1.8 to + 5.2. The radiogenic Hf isotope composition coupled with previous Sr-Nd isotope data demonstrates a significant shift from multiple crustal sources in the Sonoran batholithic belt to the predominant contribution of the mantle-derived magmas in the southwest Chihuahua and northern Sinaloa. Based on U-Pb ages, the absence of inheritance, typical high Th/U ratio and radiogenic Hf isotope composition, we suggest that the Late Cretaceous-Paleogene magmatic rocks in this region are not derived from

  17. Zircon U-Pb geochronology,Hf isotopic composition and geological implications of the rhyodacite and rhyodacitic porphyry in the Xiangshan uranium ore field,Jiangxi Province,China

    Institute of Scientific and Technical Information of China (English)


    The Xiangshan uranium ore field is the largest volcanic rock hosted uranium deposit in China.The host rock is a volcanic intrusive complex,including rhyodacite,porphyroclastic lava and late stage sub-volcanic rocks.In this study,zircons from an early stage rhyodacite and a late stage rhyodacite porphyry were dated by SHRIMP and LA-ICP-MS U-Pb methods,and their Hf isotopic compositions were measured by LA-MC-ICP-MS.206Pb/238U ages of 135.1±1.7 and 134.8±1.1 Ma were obtained for the rhyodacite and rhyodacitic porphyry,respectively.These accurate ages indicate that the Xiangshan volcanic-intrusive complex formed in the Early Cretaceous rather than in the Late Jurassic,as concluded in some previous studies.By the Early Cretaceous,the tectonic setting of the area has evolved into a back-arc extensional setting,possibly related to subduction of the paleo-Pacific plate.The close ages of the(early) eruptive rhyodacite and the(late) hypabyssal rhyodacitic porphyry shows that the Xiangshan volcanism was intensive and concentrated in a short time.Zircons from the rhyodacite show negative εHf(t) values of-5.7 to-8.5,with Hf depleted mantle model ages between 1550 and 1720 Ma,whereas zircons from the rhyodacitic porphyry yield εHf(t) values of-6.9 to-10.1 and Hf model ages between 1621 and 1823 Ma.These zircon Hf model ages are similar to the whole rock Nd model ages(1486 to 1911 Ma).Combined with other geochemical characteristics,the Xiangshan rhyodacite and rhyodacitic porphyry may have been derived from partial melting of the Paleo-Mesoproterozoic metamorphic rocks from the Xiangshan basement,without any significant addition of mantle-derived magma.Contribution of basement of this age is also supported by finding a Paleoproterozoic xenocrystic zircon core in the rhyodacite sample.

  18. Tracing magma sources of three different S-type peraluminous granitoid series by in situ U-Pb geochronology and Hf isotope zircon composition: The Variscan Montes de Toledo batholith (central Spain) (United States)

    Merino Martínez, E.; Villaseca, C.; Orejana, D.; Pérez-Soba, C.; Belousova, E.; Andersen, T.


    Three distinct S-type peraluminous granitoid types have been identified within the Variscan Montes de Toledo batholith, located in the Central Iberian Zone (SW European Variscides): type-1, extremely high peraluminous restite-rich granitoids; type-2, highly peraluminous restite-bearing granitoids; and type-3, moderately peraluminous granitoids with mafic microgranular enclaves. Type-1 and type-2 granitoids are restricted to the western part of the batholith, whereas type-3 granites are mostly restricted to the eastern segment. There is a sequential youngering of emplacement age from type-1 (late-tectonic) to type-2 and type-3 granitoids (post-tectonic), extending the timing of the batholith formation for about 19 Ma between 316 and 297 Ma. Although the degree of peraluminousity of the different series could be related to different partial melting conditions or to the variable entrainment of restitic components (including the peritectic mineral assemblage of the melting reactions), whole-rock geochemical signatures and isotope zircon composition of the peraluminous granitoid types suggest contribution of different crustal sources. There is no evidence for the direct mantle-derived material contribution in the genesis of these peraluminous melts. Type-1 and type-2 granitoids contain mostly Archean to Neoproterozoic inherited zircons, whereas type-3 granites show preferentially Neoproterozoic (up to late Cryogenian) and Ordovician inheritance. The wide range of initial Hf isotope composition, ranging to highly radiogenic values (ƐHf up to + 10), of Neoproterozoic zircon inheritances in type-1 and type-2 granitoids suggests derivation from heterogeneous Neoproterozoic metasedimentary sources composed of both juveline and recycled crustal materials, similar in composition to the host Schist-Greywacke Complex metasediments. Trace-element modelling clearly suggests the involvement of metasediments similar to those mentioned from the southern part of the Central Iberian

  19. The Yellowstone hotspot in space and time: Nd and Hf isotopes insilici magmas

    Energy Technology Data Exchange (ETDEWEB)

    Nash, Barbara P.; Perkins, Michael E.; Christensen, John N.; Lee,Den-Chuen; Halliday, A.N.


    Over the course of its 16 m.y. history, the Yellowstonehotspot has produced silicic magmas exhibiting systematic, and oftensympathetic, variations in isotopic and chemical composition, temperatureand frequency of eruption. Nd and Hf isotopic ratios vary systematicallyfrom initial eruptions at ~;16 Ma, contemporaneous with basalticvolcanism in eastern Oregon and Washington, to the present dayYellowstone Volcanic Plateau. Nd and Hf isotopic ratios co-vary and spanthe range of most terrestrial samples, reflecting mixing of mantle andcrustal sources. Earliest erupted silicic magmas were hot (in excess of1050oC), relatively less evolved and have isotopic ratios within therange of contemporaneous Columbia River flood basalts. The transit of thehotspot across the lithospheric boundary between the western accretedoceanic terrain and the Precambrian craton at 15 Ma is marked by shiftsin eNd from +4 to -11 and in ?Hf from +10 to -10. The duration of thetransit yields a crustal magma source diameter of ~;70 km. In theinterval from 14 to 9 Ma, ?Nd systematically increases from -11 to -7,recording a minimum increase in the mantle component from 5 percent to 30percent. The mantle component could be twice as great, depending upon theisotopic composition of crust and mantle reservoirs. In this sameinterval, peak temperatures of ~;1000oC occurred at 9 Ma. The last 8 m.y.are characterized by less frequent eruption of lower temperature(830-900oC) and more compositionally evolved magmas.

  20. Hf isotope evidence for effective impact melt homogenisation at the Sudbury impact crater, Ontario, Canada (United States)

    Kenny, Gavin G.; Petrus, Joseph A.; Whitehouse, Martin J.; Daly, J. Stephen; Kamber, Balz S.


    We report on the first zircon hafnium-oxygen isotope and trace element study of a transect through one of the largest terrestrial impact melt sheets. The differentiated melt sheet at the 1.85 Ga, originally ca. 200 km in diameter Sudbury impact crater, Ontario, Canada, yields a tight range of uniform zircon Hf isotope compositionsHf(1850) of ca. -9 to -12). This is consistent with its well-established crustal origin and indicates differentiation from a single melt that was initially efficiently homogenised. We propose that the heterogeneity in other isotopic systems, such as Pb, in early-emplaced impact melt at Sudbury is associated with volatility-related depletion during the impact cratering process. This depletion leaves the isotopic systems of more volatile elements more susceptible to contamination during post-impact assimilation of country rock, whereas the systems of more refractory elements preserve initial homogeneities. Zircon oxygen isotope compositions in the melt sheet are also restricted in range relative to those in the impacted target rocks. However, they display a marked offset approximately one-third up the melt sheet stratigraphy that is interpreted to be a result of post-impact assimilation of 18O-enirched rocks into the base of the cooling impact melt. Given that impact cratering was a more dominant process in the early history of the inner Solar System than it is today, and the possibility that impact melt sheets were sources of ex situ Hadean zircon grains, these findings may have significance for the interpretation of the early zircon Hf record. We speculate that apparent εHf-time arrays observed in the oldest terrestrial and lunar zircon datasets may be related to impact melting homogenising previously more diverse crust. We also show that spatially restricted partial melting of rocks buried beneath the superheated impact melt at Sudbury provided a zircon crystallising environment distinct to the impact melt sheet itself.

  1. U-Pb Zircon Ages,Geochemical and Sr-Nd-Hf Isotopic Compositions of Granitoids in Western Songpan-Garze Fold Belt: Petrogenesis and Implication for Tectonic Evolution

    Institute of Scientific and Technical Information of China (English)

    Cai Hongming; Zhang Hongfei; Xu Wangchun


    Granitoids are widespread in the Songpan-Garze (松潘-甘孜) fold belt,western China.These granitoids provide insight into regional tectono-magmatic events,basement nature and tectonic evolution.However,previous studies mainly focused on the eastern Songpan-Garze fold belt In this article,five granitoid intrusions from the western Songpan-Garze fold belt have been studied.These intrusions are composed of quartz-diorite and granodiorite.Using LA-ICP-MS zircon dating method,the obtained magma crystallization ages are 219±2 Ma for the quartz-diorite and 216±5 Ma for the granodiorite.The ages,combined with regional geological analyses,show that they formed in a post-collisional tectonic setting.The quartz-diorite and granodiorite display co-linear variation in their chemical compositions.REE compositions for both the quartz-diorite and granodiorite show strongly fractionated patterns with (La/Yb)N=5.02-18.34 and Eu/Eu*=0.44-0.89.The quartz-diorites have initial 87Sr/86Sr ratios (7Sr) of 0.709 29-0.711 97 and εNd(t) values of -8.6 to -6.1 and the granodiorites have Isr values of 0.705 49-0.709 97 and εNd(t) values of -8.3 to -4.3.Zircon Hf isotopic data show εHr(t) values of -3.8 to +1.6 for the quartz-diorites and -1.2 to +3.0 for the granodiorites.Geochemical and Sr-Nd-Hf isotopic compositions indicate that the quartz-diorites and granodiorites have similar petrogenesis.We suggest that the magmas for the quartz-diorites and granodiorites were derived from partial melting of lower crustal mafic source,resulting from amphibole dehydration melting reaction.The probing of the magma source reveals that the western Songpan-Garze fold belt contains an unexposed continental basement,which is similar to the eastern Songpan-Garze fold belt.Geodynamically,it is proposed that a lithospheric delamination model can account for the magma generation for the quartz-diorites and granodiorites in the western Songpan-Garze fold belt.

  2. Subduction Contributions in the Trans-Mexican Volcanic Belt: Implications from Lava Chemistry and Hf-Nd-Pb Isotopes (United States)

    Cai, Y.; Goldstein, S. L.; Langmuir, C. H.; Gómez-Tuena, A.; Lagatta, A.; Straub, S. M.; Martín Del Pozzo, A.


    Despite thick continental crust, near primitive lavas erupt throughout the Trans-Mexican Volcanic Belt (TMVB). In order to distinguish and better constrain subduction contributions and effects of crustal contamination, we analyzed samples representing subducting sediments from DSDP Site 487, and Quaternary lavas from stratovolcanoes and cinder cones, including alkaline "high-Nb" lavas from the Sierra Chichinautzin Volcanic Field (SCVF) showing negligible subduction signature in its trace element chemistry and representing melts of the mantle wedge. Our primary observations and implications are: (1) The high-Nb SCVF `intraplate' lavas define a linear trend along the "Nd-Hf mantle-crust array", defining the composition of the mantle wedge. (2) Popocatepetl and Nevado de Toluca stratovolcanoes show the highest Nd and Hf isotope ratios, higher than the `intraplate' lavas, indicating their sources are more "depleted mantle-like" than the regional mantle wedge. (3) The Popo and Toluca chemical and isotopic trends sharply contrast with Pico de Orizaba, which shows classic indications of crustal contamination (e.g. high 207Pb/204Pb, low Nd-Hf isotope ratios), consistent with contamination by local Precambrian crust. (4) Higher Nd-Hf isotopes in Popo and Toluca lavas also correlate with lower Pb isotope ratios, and lower Lu/Hf and Zr/Hf. Together, these data indicate contributions from subducted Pacific oceanic crust and hydrothermal sediment. (5) Popo and Toluca are also enriched in Th/LREE compared with `intraplate' lavas, reflecting subducted sediment contributions. (6) Nd-Hf isotope ratios of hydrothermal sediment from DSDP Site 487 lie on the "seawater array", with high Hf isotope ratios compared to the "mantle-crust array". Popo and Toluca Nd-Hf isotopes display a shallower slope than the "intraplate lava Nd-Hf array", reflecting contributions from hydrothermal sediment. Popocatepetl and Toluca lavas therefore avoid substantial crustal contamination of mantle wedge

  3. Detrital zircon evidence for Hf isotopic evolution of granitoid crust and continental growth (United States)

    Iizuka, Tsuyoshi; Komiya, Tsuyoshi; Rino, Shuji; Maruyama, Shigenori; Hirata, Takafumi


    We have determined U-Pb ages, trace element abundances and Hf isotopic compositions of approximately 1000 detrital zircon grains from the Mississippi, Congo, Yangtze and Amazon Rivers. The U-Pb isotopic data reveal the lack of >3.3 Ga zircons in the river sands, and distinct peaks at 2.7-2.5, 2.2-1.9, 1.7-1.6, 1.2-1.0, 0.9-0.4, and uniformitarian secular change in Hf isotopes of granitoid crusts; Hf isotopic compositions of granitoid crusts deviate from the mantle evolution line from about 3.3 to 2.0 Ga, the deviation declines between 2.0 and 1.3 Ga and again increases afterwards. Consideration of mantle-crust mixing models for granitoid genesis suggests that the noted isotopic trends are best explained if the rate of crust generation globally increased in two stages at around (or before) 3.3 and 1.3 Ga, whereas crustal differentiation was important in the evolution of the continental crust at 2.3-2.2 Ga and after 0.6 Ga. Reconciling the isotopic secular change in granitoid crust with that in sedimentary rocks suggests that sedimentary recycling has essentially taken place in continental settings rather than active margin settings and that the sedimentary mass significantly grew through addition of first-cycle sediments from young igneous basements, until after ˜1.3 Ga when sedimentary recycling became the dominant feature of sedimentary evolution. These findings, coupled with the lack of zircons older than 3.3 Ga in river sands, imply the emergence of large-scale continents at about 3.3 Ga with further rapid growth at around 1.3 Ga. This resulted in the major growth of the sedimentary mass between 3.3 and 1.3 Ga and the predominance of its cannibalistic recycling later.

  4. Atomic Weights and Isotopic Compositions (United States)

    SRD 144 Atomic Weights and Isotopic Compositions (Web, free access)   The atomic weights are available for elements 1 through 111, and isotopic compositions or abundances are given when appropriate.

  5. 锡林浩特杂岩中斜长角闪岩锆石U-Pb年代学及Hf同位素研究%U-Pb Dating and Hf Isotopic Composition of Zircons in Amphibolite from the Xilinhot Complex

    Institute of Scientific and Technical Information of China (English)

    王善辉; 陈岳龙; 李大鹏


    206Pb/238U-Pb ages is (316 ±4) Ma, which indicates the Xilinhot complex should not be Precambrian. According to the field observations and petrography, the complex may be a suite of Late Paleozoic volcanic-sedimentary formation which had been subjected to strong deformation and metamorphism. According to the zircon Hf isotopic compositions of plagioclase amphibolite in the Xilinhot complex, εHι(t) value is positive ( + 4. 1 to + 17. 0) , it should have originated from the depleted mantle or crust-mantle mixing source. A mixing calculating of depleted mantle and ancient crustal end-members based on zircon Hf isotopic compositions shows that depleted mantle-derived accretion component was dominant in the plagioclase amphibolite ( after calculation, the crust to mantle mixing ratio is about 1:2). Part of the zircons model ages between 1. 8 Ga and 2. 5 Ga suggests that Paleoproterozoic crustal materials mixed with depleted mantle-derived component during the formation process of the protolith of the plagioclase amphibolite. Comparison of the Hf model age of the plagioclase amphibolite to those in the Hinggan-Mongolia Orogenic Belt shows that crustal component in the plagioclase amphibolite originated from the Hinggan-Mongolia Orogenic Belt. Almost consistent Hf model ages with those of zircon U-Pb dating suggest that the crustal accretion event took place in Late Palaeozoic.

  6. In situ simultaneous determination of trace elements,U-Pb and Lu-Hf isotopes in zircon and baddeleyite

    Institute of Scientific and Technical Information of China (English)

    XIE LieWen; ZHANG YanBin; ZHANG HuiHuang; SUN JingFeng; WU FuYuan


    This paper describes a combined method of simultaneously measuring U-Pb and Lu-Hf isotopes as well as trace elements in Phalaborwa baddeleyite and 91500, GJ-1, TEMORA-1 and SK10-2 zircons by means of Neptune MC-ICPMS and Agilent Q-ICPMS connected to a 193 nm excimer laser ablation system. Material ablated by laser was carried in different proportions into Q-ICPMS for U-Pb isotopic and trace elemental and MC-ICPMS for Lu-Hf isotopic compositions. Experiments indicate that different propor-tions of ablated material for the Q-ICPMS and MC-ICPMS (6∶4, 5∶5 and 4∶6 respectively) do not show any bias for the zircon/baddeleyite U-Pb age, Lu-Hf isotope and trace elemental compositions within ana-lytical errors. Using 40-60 μm spot size, the obtained U-Pb ages of Phalaborwa baddeleyite, 91500, GJ-1, TEMORA and SK10-2 zircons are 2065~15 (2σ, n=20), 1063±6 (2σ, n=19), 613±6 (2σ,=20), 416±5 (2σ, n=20) and 32.6±0.5 (2σ, n=20) Ma, respectively. The 176Hf/177Hf ratios are 0.281231±24 (2SD, n=20), 0.282310±35 (2SD, n=19), 0.282028±34 (2SD, n=20), 0.282687±34 (2SD, n=20) and 0.282752±53 (2SD, n=20), respectively. The obtained trace elemental compositions are identical to the reference values. Therefore, this kind of technique makes it possible to simultaneously obtain the U-Pb age, Lu-Hf iso-topes and trace elemental compositions of zircon and baddeleyite, which could be an important tool in solving problems in earth sciences.

  7. Detrital zircon U-Pb age and Hf isotopic composition from foreland sediments of the Assam Basin, NE India: Constraints on sediment provenance and tectonics of the Eastern Himalaya (United States)

    Vadlamani, Ravikant; Wu, Fu-Yuan; Ji, Wei-Qiang


    Synorogenic Palaeogene-Neogene sediments of the Assam foreland basin, were derived by erosion of adjacent crustal and orogenic sources following the Greater India-Eurasia collision since ∼55 Ma. To constrain source sediment influx, and its relation to Himalayan tectonics, from pre- to post-collision time, detrital zircon U-Pb geochronology and their Hf isotopic compositions were carried out. The varying detrital zircon spectral patterns analyzed from the Paleogene Jaintia, Barail and Neogene Surma and Tipam Groups, with sediment petrography, track source sediment derived from cratonic India, Gangdese and eastern Transhimalayan batholiths and the eastern Himalaya. These sources are tested against Cenozoic paleopositions proposed for the northeastward motion of the Indian plate. Precollisional cratonic detritus to Middle to Late Eocene Sylhet Formation shifted to Tethyan Himalaya and arc sources of the Gangdese and eastern Transhimalayan batholiths to Late Eocene Kopili and Barail Formations, consistent with the proposed paleoposition proximal to the Indus-Yarlung suture. This Sylhet-Kopili Formation transition, within the Jaintia Group, reflects one of the earliest Himalayan hinterland exhumation stages during the Late Eocene. Major shift in provenance to Higher Himalayan Crystalline and arc detritus is recorded from the Surma Group, constraining Mid Miocene Himalayan tectonic exhumation from the eastern Himalaya. Late Miocene Tipam Group preserves sediment of Higher Himalayan Crystalline detritus, ophiolite and likely Lesser Himalayan rocks.

  8. Petrogenesis of the Neoproterozoic bimodal volcanic rocks along the western margin of the Yangtze Block: New constraints from Hf isotopes and Fe/Mn ratios

    Institute of Scientific and Technical Information of China (English)

    LI Xianhua; QI Changshi; LIU Ying; LIANG Xirong; TU Xianglin; XIE Liewen; YANG Yueheng


    High-precision major element and Hf isotope data are reported for the Neoproterozoic Suxiong volcanic rocks along the western margin of the Yangtze Block. These volcanic rocks have variable εHf(T) values and Fe/Mn ratios. The relatively primitive basalts have high Fe/Mn ratios and high Hf-Nd isotopic compositions, indicating that they were generated by partial melting of garnet clinopyroxene in mantle plume at high pressure. Thus, the Suxiong basalts are genetically related to the proposed Neoproterozoic superplume. On the contrary, a few differentiated basalts have low Fe/Mn ratios and low Hf-Nd isotopic compositions. They are likely to experience assimilation-fractional crystallization process. The Suxiong rhyolites have consistent Hf and Nd model ages of 1.3-1.4 Ga. They are likely generated by shallow dehydration melting of pre-existing young arc igneous rocks associated with the basaltic underplating/intrusion in a continental rift.

  9. Magmatic and crustal differentiation history of granitic rocks from Hf-O isotopes in zircon. (United States)

    Kemp, A I S; Hawkesworth, C J; Foster, G L; Paterson, B A; Woodhead, J D; Hergt, J M; Gray, C M; Whitehouse, M J


    Granitic plutonism is the principal agent of crustal differentiation, but linking granite emplacement to crust formation requires knowledge of the magmatic evolution, which is notoriously difficult to reconstruct from bulk rock compositions. We unlocked the plutonic archive through hafnium (Hf) and oxygen (O) isotope analysis of zoned zircon crystals from the classic hornblende-bearing (I-type) granites of eastern Australia. This granite type forms by the reworking of sedimentary materials by mantle-like magmas instead of by remelting ancient metamorphosed igneous rocks as widely believed. I-type magmatism thus drives the coupled growth and differentiation of continental crust.

  10. Geochronology and Sr–Nd–Hf isotopic composition of the granites, enclaves, and dikes in the Karamay area, NW China: Insights into late Carboniferous crustal growth of West Junggar

    Directory of Open Access Journals (Sweden)

    Di Li


    Full Text Available New whole-rock major and trace elements, and zircon U–Pb and Hf–Nd isotope compositions are reported for the Karamay dikes, enclaves, and host granites in the West Junggar, NW China. Zircon U–Pb dating of the Karamay pluton yields an age of 300.7 ± 2.3 Ma for the enclave and 300.0 ± 2.6 Ma for the host granite, which was intruded by dike with an age of 298 Ma. The host granites exhibit relatively low SiO2 contents and A/CNK and Ga/Al ratios, low initial 87Sr/86Sr ratios (0.703421–0.703526 and positive εHf(t (5.5–14.1 and εNd(t (7.3–8.1 values with a young model age, suggesting that they are I-type granites and were mainly derived from a juvenile lower crustal source. The enclaves and dikes belong to an andesitic calc-alkaline series and have high MgO concentrations at low silica content and positive εHf(t (7.6–13.2, 14.2–14.9 and εNd(t (6.8–8.3, ∼6.9 values. They are enriched in LILEs (Rb, Ba and U and LREE and depleted in HFSEs (Nb and Ta with insignificant negative Eu anomalies, indicating that the melts were derived from an enriched lithospheric mantle modified by subducted oceanic crust-derived melts and minor fluids, followed by fractional crystallization. The Karamay host granites and enclaves are of mixed origin and are most probably formed by the interaction between the lower crust- and lithospheric mantle-derived magmas, and were intruded by the unmixed dikes subsequently. The upwelling mantle through a slab window in an island arc environment might have triggered partial melting of the lithospheric mantle and its subsequent interaction with the granitic magma, further suggesting that the ridge subduction played an important role in the crustal growth of West Junggar.

  11. Hf isotope evidence for variable slab input and crustal addition in basalts and andesites of the Taupo Volcanic Zone, New Zealand

    DEFF Research Database (Denmark)

    Waight, Tod Earle; Troll, Valentin R.; Gamble, J.A.


    variations likely represent variability in primary magma compositions as a result of different degrees of sediment addition at the slab-wedge interface. Coupled variations in isotopic composition, LILE/HFSE ratios (e.g. Rb/Zr and Ba/La) and SiO2 also clearly indicate that shallower level crustal interactions......Crustal contamination complicates the identification of primary mantle-derived magma compositions in Continental arcs. However,when crustal processes and components arewell characterised, it is possible to extrapolate through continental arc magma compositional arrays towards the Hf and Nd isotope...... compositions of uncontaminated primary magmas. This is because of the similar behaviour of Hf and Nd during fractional crystallisation and mantle melting, and the subsequent limited variation in Hf/Nd in mantle-derived magmas and in many crustal lithologies, resulting in linear contamination trends for Hf...

  12. Comprehensive Pb-Sr-Nd-Hf isotopic, trace element, and mineralogical characterization of mafic to ultramafic rock reference materials (United States)

    Fourny, Anaïs.; Weis, Dominique; Scoates, James S.


    Controlling the accuracy and precision of geochemical analyses requires the use of characterized reference materials with matrices similar to those of the unknown samples being analyzed. We report a comprehensive Pb-Sr-Nd-Hf isotopic and trace element concentration data set, combined with quantitative phase analysis by XRD Rietveld refinement, for a wide range of mafic to ultramafic rock reference materials analyzed at the Pacific Centre for Isotopic and Geochemical Research, University of British Columbia. The samples include a pyroxenite (NIM-P), five basalts (BHVO-2, BIR-1a, JB-3, BE-N, GSR-3), a diabase (W-2), a dolerite (DNC-1), a norite (NIM-N), and an anorthosite (AN-G); results from a leucogabbro (Stillwater) are also reported. Individual isotopic ratios determined by MC-ICP-MS and TIMS, and multielement analyses by HR-ICP-MS are reported with 4-12 complete analytical duplicates for each sample. The basaltic reference materials have coherent Sr and Nd isotopic ratios with external precision below 50 ppm (2SD) and below 100 ppm for Hf isotopes (except BIR-1a). For Pb isotopic reproducibility, several of the basalts (JB-3, BHVO-2) require acid leaching prior to dissolution. The plutonic reference materials also have coherent Sr and Nd isotopic ratios (<50 ppm), however, obtaining good reproducibility for Pb and Hf isotopic ratios is more challenging for NIM-P, NIM-N, and AN-G due to a variety of factors, including postcrystallization Pb mobility and the presence of accessory zircon. Collectively, these results form a comprehensive new database that can be used by the geochemical community for evaluating the radiogenic isotope and trace element compositions of volcanic and plutonic mafic-ultramafic rocks.

  13. Correlated cosmogenic W and Os isotopic variations in Carbo and implications for Hf-W chronology (United States)

    Qin, Liping; Dauphas, Nicolas; Horan, Mary F.; Leya, Ingo; Carlson, Richard W.


    An obstacle for establishing the chronology of iron meteorite formation using 182Hf-182W systematics (t1/2 = 8.9 Myr) is to find proper neutron fluence monitors to correct for cosmic ray modification of W isotopic composition. Recent studies showed that siderophile elements such as Pt and Os could serve such a purpose. To test and calibrate these neutron dosimeters, the isotopic compositions of W and Os were measured in a slab of the IID iron meteorite Carbo. This slab has a well-characterized noble gas depth profile reflecting different degrees of shielding to cosmic rays. The results show that W and Os isotopic ratios correlate with distance from the pre-atmospheric center. Negative correlations, barely resolved within error, were found between ε190Os-ε189Os and ε186Os-ε189Os with slopes of -0.64 ± 0.45 and -1.8(+1.9/-2.1), respectively. These Os isotope correlations broadly agree with model predictions for capture of secondary neutrons produced by cosmic ray irradiation and results reported previously for other groups of iron meteorites. Correlations were also found between ε182W-ε189Os (slope = 1.02 ± 0.37) and ε182W-ε190Os (slope = -1.38 ± 0.58). Intercepts of these two correlations yield pre-exposure ε182W values of -3.32 ± 0.51 and -3.62 ± 0.23, respectively (weighted average ε182W = -3.57 ± 0.21). This value relies on a large extrapolation leading to a large uncertainty but gives a metal-silicate segregation age of -0.5 ± 2.4 Myr after formation of the solar system. Combining the iron meteorite measurements with simulations of cosmogenic effects in iron meteorites, equations are presented to calculate and correct for cosmogenic effects on 182W using Os isotopes.

  14. Distribution coefficients of 60 elements on TODGA resin: application to Ca, Lu, Hf, U and Th isotope geochemistry. (United States)

    Pourmand, Ali; Dauphas, Nicolas


    Batch equilibration experiments are conducted to measure the distribution coefficients (K(d)) of a large number of elements in nitric, nitric plus hydrofluoric, and hydrochloric acids on Eichrom TODGA extraction chromatography resin. The K(d)s are used to devise a multi-element extraction scheme for high-precision elemental and isotopic analyses of Ca, Hf, Lu, Th and U in geological materials, using high-purity lithium metaborate (LiBO(2)) flux fusion that allows rapid digestion of even the most refractory materials. The fusion melt, dissolved in nitric acid, is directly loaded to a TODGA cartridge on a vacuum chamber for elemental separation. An Ln-Spec cartridge is used in tandem with TODGA for Lu purification. The entire procedure, from flux digestion to preparation for isotopic analysis, can be completed in a day. The accuracy of the proposed technique is tested by measuring the concentrations of Ca (standard bracketing), Hf, Lu, Th and U (isotope dilution), and the isotopic composition of Hf in geostandards (USNM3529, BCR-2, BHVO-1, AGV-1 and AGV-2). All measurements are in excellent agreement with recommended literature values, demonstrating the effectiveness of the proposed analytical procedure and the versatility of TODGA resin.

  15. Hf Isotope Composition and REE Pattern of Zircons from Early Precambrian Metamorphic Rocks in the Daqing Mountains, Inner Mongolia%内蒙古大青山地区早前寒武纪变质岩的锆石Hf同位素组成和稀土模式

    Institute of Scientific and Technical Information of China (English)

    董春艳; 刘敦一; 万渝生; 徐仲元; 王伟; 颉颃强


    This paper reports Hf isotope and REE composition of zircons from metamorphic rocks in the Daqing Mountains, Inner Mongolia. Detrital zircons from two meta - sedimentary rock samples have [n(176Hf)/n(177Hf)]c, tDM1(Hf) and tDM2(Hf) ranging from 0. 281079~0. 281502, 2548~3000 Ma and 2612 ~ 3153 Ma and from 0. 280916 ~0. 281451, 2533 ~ 2717 Ma and 2600 ~ 3404 Ma, respectively. The eHf (t) and tym (Hf) of magmatic zircon from one meta-gabbro sample range from-5. 45 -6.68 and 2319-2647 Ma, respectively. These indicate that late Neoarhcaean - early Palaeoproterozoic tectono-magmatic events occurred in the Daqing Mountains and adjacent areas, with both mantle addition and crustal recycling. Metamorphic zircon rims commonly show young tDM2 (Hf) when comparing with detrital and magmatic zircon cores, suggesting that Lu-Hf compositions of the rocks and minerals were changed during metamorphic processes. Metamorphic zircon rims are similar in REE pattern to adjacent detrital and magmatic cores, but commonly being lower in total REE content. Most of the metamorphic rims are smaller than 0. 1 in Th/U ratio, being quite different from the cores which Th/U ratios are generally higher than 0. 5. It is speculated that metamorphic fluid was high in w(176Hf)/w(177Hf) ratio and U and low in Th and REE and played an important role in metamorphic zircon formation.%本文报道了内蒙古大青山地区早前寒武纪变质岩石的锆石Hf同位素和稀土组成.两个古元古代晚期(1.9~2.1 Ga)变质碎屑沉积岩样品中碎屑锆石的[n(176Hf)/n(177Hf)]c、tDM1(Hf)和tDM2(Hf)分别为0.281079~0.281502、2548~3000 Ma、2612~3153 Ma和0.280g16~0.281451、2533~2717 Ma、2600~3404 Ma;一个古元古代早期(2.37 Ga)变质辉长岩样品中岩浆锆石的εHf(t)和tDM1(Hf)分别为1.50~6.68和2449~2647 Ma,表明大青山及邻区在新太古代晚期-古元古代早期存在强烈的构造岩浆热事件,既有地幔添加又有壳内再循环作用.三个样

  16. Sr-Nd-Pb-Hf isotope systematics of the Hugo Dummett Cu-Au porphyry deposit (Oyu Tolgoi, Mongolia) (United States)

    Dolgopolova, A.; Seltmann, R.; Armstrong, R.; Belousova, E.; Pankhurst, R. J.; Kavalieris, I.


    Major and trace element geochemistry including Sr-Nd-Pb-Hf isotopic data are presented for a representative sample suite of Late Devonian to Early Carboniferous plutonic and volcanic rocks from the Hugo Dummett deposit of the giant Oyu Tolgoi porphyry Cu-Au district in South Gobi, Mongolia. Sr and Nd isotopes (whole-rock) show restricted ranges of initial compositions, with positive ɛNdt mainly between + 3.4 and + 7.4 and (87Sr/86Sr)t predominantly between 0.7037 and 0.7045 reflecting magma generation from a relatively uniform juvenile lithophile-element depleted source. Previously dated zircons from the plutonic rocks exhibit a sample-averaged range of ɛHft values of + 11.6 to + 14.5. Depleted-mantle model ages of 420-830 (Nd) and 320-730 Ma (zircon Hf) limit the involvement of pre-Neoproterozoic crust in the petrogenesis of the intermediate to felsic calc-alkaline magmas to, at most, a minor role. Pb isotopes (whole-rock) show a narrow range of unradiogenic initial compositions: 206Pb/204Pb 17.40-17.94, 207Pb/204Pb 15.43-15.49 and 208Pb/204Pb 37.25-37.64, in agreement with Sr-Nd-Hf isotopes indicating the dominance of a mantle component. All four isotopic systems suggest that the magmas from which the large Oyu Tolgoi porphyry system was generated originated predominantly from juvenile material within the subduction-related setting of the Gurvansayhan terrane.

  17. Geochemical proxies of ocean circulation and weathering inputs: Radiogenic isotopes of Nd, Pb, Sr, Hf, and Os

    Energy Technology Data Exchange (ETDEWEB)

    Frank, Martin, E-mail: [IFM-GEOMAR, Leibniz Institute of Marine Sciences at the University of Kiel, Wischhofstrasse 1-3, 24148 Kiel (Germany)


    Marine records of the radiogenic isotope composition of the elements neodymium (Nd), lead (Pb), hafnium (Hf), strontium (Sr), and osmium (Os) allow the reconstruction of past continental weathering inputs on different time scales as a function of their respective oceanic residence times. Sr and Os have oceanic residence times significantly longer than the global mixing time of the ocean and are efficiently mixed on a global scale. Their isotope composition changes on long time scales as a function of plate tectonics and major orogenies, which allows their use as precise stratigraphic tools for the entire Phanerozoic. In contrast, Hf, Pb, and in particular Nd, have residence times on the order of or shorter than the global mixing time of the ocean, which results in distinct isotopic signatures of water masses and allows the reconstruction of past water mass mixing and weathering inputs on both long and short time scales. Here applications of these isotopes systems with a focus on the shorter residence time tracers are reviewed (without claiming to be comprehensive) and problems and potential solutions are discussed.

  18. Paleoproterozoic basement beneath the southern Jiangxi Province: Evidence from U-Pb ages and Lu-Hf isotopes in zircons from the Doushui Iamprophyre

    Institute of Scientific and Technical Information of China (English)

    YU JinHai; WANG LiJuan; O'REILLY S Y; SHU LiangShu; UN Tao


    This paper presents geochemical analyses of a lamprophyre intruding the Caledonian Doushui granite body in Shangyou County, southern Jiangxi Province. U-Pb dating and Hf-isotope analyses are especially carried out for zircons from it. Petrological and geochemical features show that the lamprophyre belongs to a high-K, weakly alkaline pyroxene-biotite iamprophyre. It is characterized by high Mg# (0.74),Ni (253 μg/g) and Cr (893 μg/g) contents, and also enriched in incompatible elements, such as REE, Rb, Sr, Ba and K. It is suggested that its primitive melt probably derived from enriched mantle metasomatized by non-crust-derived agent. Morphology and LAM-ICPMS dating results of zircons in the lam prophyre indicate that they are xenocrysts captured from deep crustal rocks. Most xenocrystic zircons formed at -1.86 Ga, and a few in different Phanerozoic periods. The Paleoproterozoic zircons are of magmatic origin and have similar 176Hf/177Hf and 176Lu/177Hf ratios, indicating that they probably are from the same igneous basement rock. The ages and Hf-isotope compositions of zircons from this basement rock are similar to those of Paleoproterozoic Danzhu granite in the southern Zhejiang Province, but extremely distinguished from the Nanling basement, suggesting that the study area probably is a westward extension part of Paleoproterozoic Wuyishan terrane in the eastern Cathaysia Block. These Paleoproterozoic zircons have low Hf-isotope compositions, characteristic of crustal source. Hf model ages of these zircons and the presence of older inherited cores within them, coupled with available other data reported by previous studies, suggest that the source of Paleoproterozoic magma is Neoarchaean crust, implying the existence of older basement in the Wuyishan terrane. U-Pb ages and Hf isotopes of five Phanerozoic zircons indicate that Paleoproterozoic basement underwent multi-reworking occurring in Caledonian, Indosinian and early Yanshanian, respectively. The Caledonian

  19. Geodynamic investigation of the processes that control Lu-Hf isotopic differences between different mantle domains and the crust (United States)

    Jones, Rosie; van Keken, Peter; Hauri, Erik; Vervoort, Jeff; Ballentine, Chris J.


    The chemical and isotopic composition of both the Earth's mantle and the continental crust are greatly influenced by subduction zone processes, such as the formation of continental crust through arc volcanism and the recycling of surface material into the deep mantle. Here we use a combined geodynamical-geochemical approach to investigate the long term role of subduction on the Lu-Hf isotopic evolution of the mantle and the continental crust. We apply the geodynamic model developed by Brandenburg et al., 2008. This model satisfies the geophysical constraints of oceanic heat flow and average plate velocities, as well as geochemical observations such as 40Ar in the atmosphere, and reproduces the geochemical distributions observed in multiple isotope systems which define the HIMU, MORB and EM1 mantle endmembers. We extend this application to investigate the detail of terrestrial Lu-Hf isotope distribution and evolution, and specifically to investigate the role of sediment recycling in the generation of EM2 mantle compositions. The model has been updated to produce higher resolution results and to include a self-consistent reorganisation of the plates with regions of up-/down-wellings. The model assumes that subduction is initiated at 4.5 Ga and that a transition from 'dry' to 'wet' subduction occurred at 2.5 Ga. The modelling suggests that the epsilon Hf evolution of the upper mantle can be generated through the extraction and recycling of the oceanic crust, and that the formation of continental crust plays a lesser role. Our future intention is to utilise the model presented here to investigate the differences observed in the noble gas compositions (e.g., 40Ar/36Ar, 3He/4He) of MORB and OIB. Brandenburg, J.P., Hauri, E.H., van Keken, P.E., Ballentine, C.J., 2008. Earth and Planetary Science Letters 276, 1-13.

  20. Refinement of the supercontinent cycle with Hf, Nd and Sr isotopes

    Directory of Open Access Journals (Sweden)

    Kent C. Condie


    External and internal orogens show similar patterns in ɛNd and ɛHf with age suggesting that both juvenile and reworked crustal components are produced in both types of orogens with similar proportions. However, both types of orogens clearly produce more juvenile isotopic signatures in retreating mode than in advancing mode. Many secular changes in ɛHf and ɛNd distributions correlate with the supercontinent cycle. Although supercontinent breakup is correlated with short-lived decreasing ɛHf and ɛNd (≤100 Myr for most supercontinents, there is no isotopic evidence for the breakup of the Paleoproterozoic supercontinent Nuna. Assembly of supercontinents by extroversion is recorded by decreasing ɛNd in granitoids and metasediments and decreasing ɛHf in zircons, attesting to the role of crustal reworking in external orogens in advancing mode. As expected, seawater Sr isotopes increase and seawater Nd isotopes decrease during supercontinent assembly by extroversion. Pangea is the only supercontinent that has a clear isotopic record of introversion assembly, during which median ɛNd and ɛHf rise rapidly for ≤100 Myr. Although expected to increase, radiogenic seawater Sr decreases (and seawater Nd increases during assembly of Pangea, a feature that may be caused by juvenile input into the oceans from new ocean ridges and external orogens in retreating mode. The fact that a probable onset of plate tectonics around 3 Ga is not recorded in isotopic distributions may be due the existence of widespread felsic crust formed prior to the onset of plate tectonics in a stagnant lid tectonic regime, as supported by Nd and Hf model ages.

  1. Age and origin of post collision Baltoro granites, south Karakoram, North Pakistan: Insights from in-situ U-Pb, Hf and oxygen isotopic record of zircons (United States)

    Mahar, Munazzam Ali; Mahéo, Gweltaz; Goodell, Philip C.; Pavlis, Terry L.


    Origin of post collision plutonism is critical to understand the tectonothermal evolution of the over thickened continental crust in collision zones. This has proven difficult to reconcile with the conventional whole rock geochemical and field based studies alone. We report in-situ study of zircon U-Pb, Hf and O isotopes from five samples of the Baltoro Plutonic Unit (BPU) in south Karakoram. The plutonic unit is the western part of the southern Asian margin of the India-Asia convergent zone. Baltoro granites and a biotite-rich enclave yielded similar and overlapping U-Pb ages ranging from 26 to 15 Ma. Hafnium isotopic compositionHf (0)) is very heterogeneous ranging from - 17.1 to + 4.4 while the oxygen isotopic composition of the granites is homogeneous with mean δ18O ranging from 7.2 to 9.4‰. Based on U-Pb geochronology and Hf-O isotopic composition, the involvement of two main sources is suggested (1) Cretaceous calc-alkaline Karakoram crust and (2) Karakoram gneisses. Moreover, possible involvement of metasomatized Asian lithospheric mantle is supported by elevated oxygen composition of granites and identical Hf composition of biotite-rich enclave to the mantle derived Baltoro lamprophyre. However, direct contribution from juvenile pristine mantle is unlikely as no juvenile mantle type Hf and oxygen values were obtained. This also precludes the involvement of southward juvenile arc related component of Kohistan-Ladakh batholith. Our new U-Pb and Hf data are comparable to the Mesozoic Karakoram batholith, Miocene two-mica leucogranites in the Pangong Range and magmatism from the Lhasa terrane in south Tibet, suggesting a genetic link between the Karakoram and the rocks to the east. This magmatic event is best explained by lower crust partial melting promoted by both thermal equilibration following crustal thickening and heat advection by ultrapotassic magmas associated with the breakoff of the Indian continental margin.

  2. 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 (United States)

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


    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/Hf

  3. A linear Hf isotope-age array despite different granitoid sources and complex Archean geodynamics: Example from the Pietersburg block (South Africa) (United States)

    Laurent, Oscar; Zeh, Armin


    Combined U-Pb and Lu-Hf isotope data from zircon populations are widely used to constrain Hadean-Archean crustal evolution. Linear Hf isotope-age arrays are interpreted to reflect the protracted, internal reworking of crust derived from the (depleted) mantle during a short-lived magmatic event, and related 176Lu/177Hf ratios are used to constrain the composition of the reworked crustal reservoir. Results of this study, however, indicate that Hf isotope-age arrays can also result from complex geodynamic processes and crust-mantle interactions, as shown by U-Pb and Lu-Hf isotope analyses of zircons from well characterized granitoids of the Pietersburg Block (PB), northern Kaapvaal Craton (South Africa). Apart from scarce remnants of Paleoarchean crust, most granitoids of the PB with ages between 2.94 and 2.05 Ga (n = 32) define a straight Hf isotope-age array with low 176Lu/177Hf of 0.0022, although they show a wide compositional range, were derived from various sources and emplaced successively in different geodynamic settings. The crustal evolution occurred in five stages: (I) predominately mafic crust formation in an intra-oceanic environment (3.4-3.0 Ga); (II) voluminous TTG crust formation in an early accretionary orogen (3.0-2.92 Ga); (III) internal TTG crust reworking and subduction of TTG-derived sediments in an Andean-type setting (2.89-2.75 Ga); (IV) (post-)collisional high-K magmatism from both mantle and crustal sources (2.71-2.67 Ga); and (V) alkaline magmatism in an intra-cratonic environment (2.05-2.03 Ga). The inferred array results from voluminous TTG crust formation during stage II, and involvement of this crust during all subsequent stages by two different processes: (i) internal crust reworking through both partial melting and assimilation at 2.89-2.75 Ga, leading to the formation of biotite granites coeval with minor TTGs, and (ii) subduction of TTG-derived sediments underneath the PB, causing enrichment of the mantle that subsequently became

  4. Coupled Hf-Nd-Pb isotope co-variations of HIMU oceanic island basalts from Mangaia, Cook-Austral islands, suggest an Archean source component in the mantle transition zone (United States)

    Nebel, Oliver; Arculus, Richard J.; van Westrenen, Wim; Woodhead, Jon D.; Jenner, Frances E.; Nebel-Jacobsen, Yona J.; Wille, Martin; Eggins, Stephen M.


    Although it is widely accepted that oceanic island basalts (OIB) sample geochemically distinct mantle reservoirs including recycled oceanic crust, the composition, age, and locus of these reservoirs remain uncertain. OIB with highly radiogenic Pb isotope signatures are grouped as HIMU (high-μ, with μ = 238U/204Pb), and exhibit unique Hf-Nd isotopic characteristics, defined as ΔɛHf, deviant from a terrestrial igneous rock array that includes all other OIB types. Here we combine new Hf isotope data with previous Nd-Pb isotope measurements to assess the coupled, time-integrated Hf-Nd-Pb isotope evolution of the most extreme HIMU location (Mangaia, French Polynesia). In comparison with global MORB and other OIB types, Mangaia samples define a unique trend in coupled Hf-Nd-Pb isotope co-variations (expressed in 207Pb/206Pb vs. ΔɛHf). In a model employing subducted, dehydrated oceanic crust, mixing between present-day depleted MORB mantle (DMM) and small proportions (˜5%) of a HIMU mantle endmember can re-produce the Hf-Nd-Pb isotope systematics of global HIMU basalts (sensu stricto; i.e., without EM-1/EM-2/FOZO components). An age range of 3.5 to affected by other enriched mantle endmembers (sensu lato). If correct, this requires isolation of parts of the mantle transition zone for >3 Gyr and implies that OIB chemistry can be used to test geodynamic models.

  5. Hf isotopes of the 3.8 Ga zircons in eastern Hebei Province, China: Implications for early crustal evolution of the North China Craton

    Institute of Scientific and Technical Information of China (English)

    WU Fuyuan; YANG Jinhui; LIU Xiaoming; LI Tiesheng; XIE Liewen; YANG Yueheng


    Zircon U-Pb dating indicates that the fuchsite quartzite in eastern Hebei Province was derived from weathering and erosion of the 3.6-3.8 Ga granitic rocks. In-situ zircon Hf analyses show that the Lu-Hf isotopic system remained closed during later thermal disturbances. Zircons with concordant ages have Hf isotopic model ages of about 3.8 Ga, suggesting a recycling of this ancient crust. The ~3.8 Ga zircons have similar Hf isotopic compositions to those of chondrite, indicating that their source rocks (granitic rocks) were derived from partial melting of the juvenile crust which originated from a mantle without significant crust-mantle differentiation. Therefore, it is proposed that there was no large-scale crustal growth before ~3.8 Ga in eastern Hebei Province. Considering zircon Hf isotopic data from other areas, it is concluded that the most ancient crust in the North China Craton probably formed at about 4.0 Ga, and the possibility to find crust older than 4.0 Ga is very limited.

  6. Erosion of Archean continents: The Sm-Nd and Lu-Hf isotopic record of Barberton sedimentary rocks (United States)

    Garçon, M.; Carlson, R. W.; Shirey, S. B.; Arndt, N. T.; Horan, M. F.; Mock, T. D.


    Knowing the composition, nature and amount of crust at the surface of the early Earth is crucial to understanding the early geodynamics of our planet. Yet our knowledge of the Hadean-Archean crust is far from complete, limited by the poor preservation of Archean terranes, and the fact that less attention has been paid to the sedimentary record that tracks erosion of these ancient remnants. To address this problem and get a more comprehensive view of what an Archean continent may have looked like, we investigated the trace element and Sm-Nd, Lu-Hf isotopic records of Archean metasedimentary rocks from South Africa. We focused our study on sandstone and mudstone from drill core in the Fig Tree Group (3.23-3.26 Ga) of the Barberton granite-greenstone belt, but also analyzed the 3.4 Ga Buck Reef cherts and still older (3.5-3.6 Ga) meta-igneous rocks from the Ancient Gneiss Complex, Swaziland. Based on principal component analysis of major and trace element data, the Fig Tree metasedimentary rocks can be classified into three groups: crustal detritus-rich sediments, Si-rich sediments and Ca-, Fe-rich sediments. The detritus-rich sediments have preserved the Sm-Nd and Lu-Hf isotopic signatures of their continental sources, and hence can be used to constrain the composition of crust eroded in the Barberton area in the Paleoarchean period. Based on Sm/Nd ratios, we estimate that this crust was more mafic than today, with an average SiO2 content of 60.5 ± 2 wt.%. This composition is further supported by isotopic mixing calculations suggesting that the sedimentary source area contained equal proportions of mafic-ultramafic and felsic rocks. This implies that the Archean crust exposed to weathering was more mafic than today but does not exclude a more felsic composition at depth. Neodymium and Hf crustal residence ages show that the eroded crust was, on average, ∼300-400 Ma older than the deposition age of the sediments, which highlights the importance of intracrustal

  7. Evolution of continental crust and mantle heterogeneity: Evidence from Hf isotopes (United States)

    Jonathan, Patchett P.; Kouvo, O.; Hedge, C.E.; Tatsumoto, M.


    We present initial 176Hf/177 Hf ratios for many samples of continental crust 3.7-0.3 Gy old. Results are based chiefly on zircons (1% Hf) and whole rocks: zircons are shown to be reliable carriers of essentially the initial Hf itself when properly chosen on the basis of U-Pb studies. Pre-3.0 Gy gneisses were apparently derived from an unfractionated mantle, but both depleted and undepleted mantle are evident as magma sources from 2.9 Gy to present. This mantle was sampled mainly from major crustal growth episodes 2.8, 1.8 and 0.7 Gy ago, all of which show gross heterogeneity of 176Hf/177Hf in magma sources from ??Hf=0 to +14, or about 60% of the variability of the present mantle. The approximate ??Hf=2??Nd relationship in ancient and modern igneous rocks shows that 176Lu/177Hf fractionates in general twice as much as 147Sm/144Nd in mantle melting processes. This allows an estimation of the relative value of the unknown bulk solid/liquid distribution coefficient for Hf. DLu/DHf=??? 2.3 holds for most mantle source regions. For garnet to be an important residual mantle phase, it must hold Hf strongly in order to preserve Hf-Nd isotopic relationships. The ancient Hf initials are consistent with only a small proportion of recycled older cratons in new continental crust, and with quasi-continuous, episodic growth of the continental crust with time. However, recycling of crust less than 150 My old cannot realistically be detected using Hf initials. The mantle shows clearly the general positive ??Hf resulting from a residual geochemical state at least back to 2.9 Gy ago, and seems to have repeatedly possessed a similar degree of heterogeneity, rather than a continuously-developing depletion. This is consistent with a complex dynamic disequilibrium model for the creation, maintenance and destruction of heterogeneity in the mantle. ?? 1981 Springer-Verlag.

  8. Magma mixing and the generation of isotopically juvenile silicic magma at Yellowstone caldera inferred from coupling 238U–230Th ages with trace elements and Hf and O isotopes in zircon and Pb isotopes in sanidine (United States)

    Stelten, Mark E.; Cooper, Kari M.; Vazquez, Jorge A.; Reid, Mary R.; Barfod, Gry H.; Wimpenny, Josh; Yin, Qing-Zhu


    The nature of compositional heterogeneity within large silicic magma bodies has important implications for how silicic reservoirs are assembled and evolve through time. We examine compositional heterogeneity in the youngest (~170 to 70 ka) post-caldera volcanism at Yellowstone caldera, the Central Plateau Member (CPM) rhyolites, as a case study. We compare 238U–230Th age, trace-element, and Hf isotopic data from zircons, and major-element, Ba, and Pb isotopic data from sanidines hosted in two CPM rhyolites (Hayden Valley and Solfatara Plateau flows) and one extracaldera rhyolite (Gibbon River flow), all of which erupted near the caldera margin ca. 100 ka. The Hayden Valley flow hosts two zircon populations and one sanidine population that are consistent with residence in the CPM reservoir. The Gibbon River flow hosts one zircon population that is compositionally distinct from Hayden Valley flow zircons. The Solfatara Plateau flow contains multiple sanidine populations and all three zircon populations found in the Hayden Valley and Gibbon River flows, demonstrating that the Solfatara Plateau flow formed by mixing extracaldera magma with the margin of the CPM reservoir. This process highlights the dynamic nature of magmatic interactions at the margins of large silicic reservoirs. More generally, Hf isotopic data from the CPM zircons provide the first direct evidence for isotopically juvenile magmas contributing mass to the youngest post-caldera magmatic system and demonstrate that the sources contributing magma to the CPM reservoir were heterogeneous in 176Hf/177Hf at ca. 100 ka. Thus, the limited compositional variability of CPM glasses reflects homogenization occurring within the CPM reservoir, not a homogeneous source.

  9. Evolution of E2 transition strength in deformed hafnium isotopes from new measurements on $^{172}$Hf, $^{174}$Hf, and $^{176}$Hf

    CERN Document Server

    Rudigier, M; Dannhoff, M; Gerst, R-B; Jolie, J; Saed-Samii, N; Stegemann, S; Régis, J-M; Robledo, L M; Rodríguez-Guzmán, R; Blazhev, A; Fransen, Ch; Warr, N; Zell, K O


    The available data for E2 transition strengths in the region between neutron-deficient Hf and Pt isotopes are far from complete. More and precise data are needed to enhance the picture of structure evolution in this region and to test state-of-the-art nuclear models. In a simple model, the maximum collectivity is expected at the middle of the major shell. However, for actual nuclei, this picture may no longer be the case, and one should use a more realistic nuclear-structure model. We address this point by studying the spectroscopy of Hf. We remeasure the 2^+_1 half-lives of 172,174,176Hf, for which there is some disagreement in the literature. The main goal is to measure, for the first time, the half-lives of higher-lying states of the rotational band. The new results are compared to a theoretical calculation for absolute transition strengths. The half-lives were measured using \\gamma-\\gamma and conversion-electron-\\gamma delayed coincidences with the fast timing method. For the determination of half-lives i...

  10. Role of mantle-derived magma in genesis of early Yanshanian granites in the Nanling Range, South China: in situ zircon Hf-O isotopic constraints

    Institute of Scientific and Technical Information of China (English)


    Although a number of petrographic observations and isotopic data suggest that magma mixing is common in genesis of many granite plutons, it is still controversial whether the mantle-derived magmas were involved in granites. We carried out in this study a systematic analysis of in situ zircon Hf-O isotopes for three early Yanshanian intrusions dated at ca. 160 Ma from the Nanling Range of Southeast China. The Qinghu monzonite has very homogeneous zircon Hf-O isotopic compositions, εHf(t) =11.6±0.3 and δ18O=5.4‰±0.3‰. In combination with whole-rock geochemical and Sr-Nd isotopic data, the parental magma of the Qinghu monzonite were likely derived from the partial melting of recently-metasomatized, phlogopite-bearing lithospheric mantle without appreciable crustal contamination. The Lisong and Fogang granites and the mafic microgranular enclaves (MME) within the Lisong granites have a wide range of zircon Hf-O isotopic compositions, with Hf and O isotopes being negatively correlated within each pluton. The Lisong MMEs were crystallized from a mantle-derived magma, similar to the parental magma of the Qinghu monzonite, with small amount of crustal assimilation. The Lisong and Fogang granites were formed by reworking of meta-sedimentary materials by mantle-derived magmas and mixing of the mantle-and sediment-derived melts to varying degrees. It is thus concluded that these two Yanshanian granites in the Nanling Range were formed associated with growth and differentiation of continental crust.

  11. Magmatic recharge buffers the isotopic compositions against crustal contamination in formation of continental flood basalts (United States)

    Yu, Xun; Chen, Li-Hui; Zeng, Gang


    Isotopic compositions of continental flood basalts are essential to understand their genesis and to constrain the character of their mantle sources. Because of potential crustal contamination, it needs to be evaluated if and to which degree these basalts record original isotopic signals of their mantle sources and/or crustal signatures. This study examines the Sr, Nd, Hf, and Pb isotopic compositions of the late Cenozoic Xinchang-Shengzhou (XS) flood basalts, a small-scale continental flood basalt field in eastern China. The basalts show positive correlations between 87Sr/86Sr and 143Nd/144Nd, and negative correlations between 143Nd/144Nd and 176Hf/177Hf, which deviate from compositional arrays of crustal contamination and instead highlight variations in magmatic recharge intensity and mantle source compositions. The lava samples formed by high-volume magmatic recharge recorded signals of recycled sediments in the mantle source, which are characterized by moderate Ba/Th (91.9-106.5), excess 208Pb/204Pb relative to 206Pb/204Pb, and excess 176Hf/177Hf relative to 143Nd/144Nd. Thus, we propose that magmatic recharge buffers the original isotopic compositions of magmas against crustal contamination. Identifying and utilizing the isotope systematics of continental flood basalts generated by high volumes of magmatic recharge are thus crucial to trace their mantle sources.

  12. Re-Os and Lu-Hf isotopic constraints on the formation and age of mantle pyroxenites from the Bohemian Massif (United States)

    Ackerman, Lukáš; Bizimis, Michael; Haluzová, Eva; Sláma, Jiří; Svojtka, Martin; Hirajima, Takao; Erban, Vojtěch


    We report on the Lu-Hf and Re-Os isotope systematics of a well-characterized suite of spinel and garnet pyroxenites from the Gföhl Unit of the Bohemian Massif (Czech Republic, Austria). Lu-Hf mineral isochrons of three pyroxenites yield undistinguishable values in the range of 336-338 Ma. Similarly, the slope of Re-Os regression for most samples yields an age of 327 ± 31 Ma. These values overlap previously reported Sm-Nd ages on pyroxenites, eclogites and associated peridotites from the Gföhl Unit, suggesting contemporaneous evolution of all these HT-HP rocks. The whole-rock Hf isotopic compositions are highly variable with initial εHf values ranging from - 6.4 to + 66. Most samples show a negative correlation between bulk rock Sm/Hf and εHf and, when taking into account other characteristics (e.g., high 87Sr/86Sr), this may be explained by the presence of recycled oceanic sediments in the source of the pyroxenite parental melts. A pyroxenite from Horní Kounice has decoupled Hf-Nd systematics with highly radiogenic initial εHf of + 66 for a given εNd of + 7.8. This decoupling is consistent with the presence of a melt derived from a depleted mantle component with high Lu/Hf. Finally, one sample from Bečváry plots close to the MORB field in Hf-Nd isotope space consistent with its previously proposed origin as metamorphosed oceanic gabbro. Some of the websterites and thin-layered pyroxenites have variable, but high Os concentrations paralleled by low initial γOs. This reflects the interaction of the parental pyroxenitic melts with a depleted peridotite wall rock. In turn, the radiogenic Os isotope compositions observed in most pyroxenite samples is best explained by mixing between unradiogenic Os derived from peridotites and a low-Os sedimentary precursor with highly radiogenic 187Os/188Os. Steep increase of 187Os/188Os at nearly uniform 187Re/188Os found in a few pyroxenites may be connected with the absence of primary sulfides, but the presence of minor

  13. Early Differentiation of the Crust-Mantle System: a Hf Isotope Perspective (United States)

    Scherer, E.; Munker, C.; Mezger, K.


    The Lu decay constant recently determined by Scherer et al. 2001 (i.e., 1.865 x 10-11 yr-1) agrees with the results of the two latest physical counting experiments (1.86 x 10-11 yr-1; Dalmasso et al 1992, Nir-El and Lavi 1998), but is ca. 4 percent lower than the decay constants that have been used throughout the Hf isotope literature (e.g., 1.94 x 10-11, Tatsumoto et al., 1981; 1.93 x 10-11 Sguigna et al, 1982). In addition to making Lu-Hf ages older by ca. 4 percent, the revised decay constant also shifts the calculated initial epsilon Hf values of early Archean and Hadean rocks and zircons that are used to constrain crust-mantle differentiation in the early Earth. The initial epsilon Hf values for low-Lu/Hf samples such as zircons and evolved felsic rocks shift downward by 2-4 epsilon units, primarily due to the shift in the position of the CHUR evolution curve rather than that of the samples themselves. Mafic rocks, such as komatiites have higher Lu/Hf ratios that are closer to that of CHUR and therefore their initial epsilon Hf values do not shift as much (up to 1.3 epsilon units lower or 0.4 epsilon units higher). Using the old decay constant, some early Archean rocks (e.g., Amitsoq gneisses; Vervoort et al., 1996, Vervoort and Blichert-Toft, 1999) seemed to have very high initial epsilon Hf values (up to +6), implying that the upper mantle was moderately depleted in the early Archean and that a substantial volume of crust was produced in the Hadean. However, when recalculated with the new decay constant, the data suggest that the mantle was only slightly depleted, requiring less early crust extraction, and allowing a later date for the onset of significant crust production. In contrast, the extremely low recalculated epsilon Hf values of Earth's oldest zircons (Amelin et al., 1999, Amelin et al., 2000) indicate that Earth's first crust formed at or before 4.3 Ga, and that this crust remained intact long enough (>200 million years) to evolve to such low

  14. Formation history and protolith characteristics of granulite facies metamorphic rock in Central Cathaysia deduced from U-Pb and Lu-Hf isotopic studies of single zircon grains

    Institute of Scientific and Technical Information of China (English)

    YU Jinhai; ZHOU Xinmin; Y. S. O'Reilly; ZHAO Lei; W. L. Griffin; WANG Rucheng; WANG Lijuan; CHEN Xiaomin


    The petrochemical as well as zircon U-Pb and Lu-Hf isotopic studies of granulite facies metamorphic rock from the Taoxi Group in eastern Nanling Range, Central Cathaysia indicate that its protolith is the sedimentary rock with low maturation index. The clastic materials are mostly from middle Neoproterozoic (~736 Ma) granitoid rocks with minor Neoarchaean and Paleoproterozoic rocks. The timing of this Neoproterozoic magmatism is in agreement with the second period of magmatism widespread surrounding the Yangtze Block. Hf isotopic data indicate that the Neoproterozoic granitoids resulted from the recycled Paleoproterozoic mantle-derived crustal materials. The sedimentary rock was deposited in Late Neoproterozoic Era, and carried into low crust in Early Paleozoic. The partial melting of the meta-sedimentary rock took place at about 480 Ma and subsequently granulite facies metamorphism occurred at ca. 443 Ma. The zircons forming during this time interval (Early Paleozoic) show large Hf isotope variations, and their -Hf(t) values increase from -13.2 to +2.36 with decreasing age, suggesting the injection of mantle-derived materials during partial melting and metamorphism processes in the Early Paleozoic. Calculation results show that this metamorphic rock, if evolved to Mesozoic, has similar isotopic composition to the nearby Mesozoic high Si peraluminous granites, implying that this kind of granulite facies metamorphic rock is probably the source material of some Mesozoic peraluminous granitoids in eastern Nanling Range.

  15. A chilling perspective on Greenland's early Cenozoic climate from coupled Hf-Nd isotopes (United States)

    Scher, H. D.; Bizimis, M.; Buckley, W. P., Jr.; Duggan, B.; Bohaty, S. M.; Wilson, P. A.


    The prevailing view of northern hemisphere glaciation has been of ice sheets forming on Greenland after 2.7 Ma, with iceberg rafting as early as 15 Ma. This view is incompatible with recent results from global climate/ice sheet models that predict northern hemisphere glaciation only after CO2 falls below ~280 ppmv (occurring at 25 Ma) and with recent sediment evidence for Arctic iceberg rafting as early as the middle Eocene. However, the amount of northern hemisphere ice represented by these sediments is ambiguous and global ice budget calculations for the early Cenozoic are controversial. Here we use coupled Hf-Nd isotopes of oxyhydroxides in sediments from the upper Eocene to lower Oligocene section in ODP Site U1411 (Newfoundland Ridge) to determine when the circum-North Atlantic came under the influence of a mechanical weathering regime. Leached oxyhydroxide Hf-Nd isotopes are an indicator of weathering intensity because mechanical weathering by ice sheets mobilizes the zircon-bound Hf reservoir in the crust, which has extreme unradiogenic eHf values. Chemical weathering produces a distinct seawater array on Hf-Nd diagrams, while seawater exposed to the products of mechanical weathering plot on divergent arrays closer to the Terrestrial Array. Hf-Nd isotopes of Site U1411 leachates are grouped in a near vertical trend between the seawater and terrestrial global reference arrays. Within this group there are four distinct arrays that can be delineated by age. Samples that are late Eocene in age fall along an array that is slightly divergent from the seawater array. The aspect of the Hf-Nd isotope data changes permanently after the first step of the EOT, falling along arrays that are systematically offset in the direction of the terrestrial arrays. The steepest array, most proximal to the terrestrial array, is comprised of samples deposited between 33.7 and 32.2 Ma. These results indicate a circum-North Atlantic weathering regime appeared in the earliest Oligocene.

  16. Plume-Lithosphere Interaction beneath the Snake River Plain, Idaho: Constraints from Pb, Sr, Nd, and Hf Isotopes (United States)

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


    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

  17. A method for combined Sr-Nd-Hf isotopic analysis of <10 mg dust samples: implication for ice core science (United States)

    Ujvari, Gabor; Wegner, Wencke; Klötzli, Urs


    Aeolian mineral dust particles below the size of 10-20 μm often experience longer distance transport in the atmosphere, and thus Aeolian dust is considered an important tracer of large-scale atmospheric circulation. Since ice core dust is purely Aeolian in origin, discrimination of its potential source region(s) can contribute to a better understanding of past dust activity and climatic/environmental causes. Furthermore, ice core dust source information provides critical experimental constraints for model simulations of past atmospheric circulation patterns [1,2]. However, to identify dust sources in past dust archives such as ice cores, the mineralogy and geochemistry of the wind-blown dust material must be characterized. While the amount of dust in marine cores or common terrestrial archives is sufficient for different types of analyses and even for multiple repeat measurements, dust content in ice cores is usually extremely low even for the peak dusty periods such as the Last Glacial Maximum (LGM) (5-8 mg dust/kg ice; [3]). Since the most powerful dust fingerprinting methods, such as REE composition and Sr-Nd-Pb isotopic analyses are destructive there is a clear need to establish sequential separation techniques of Sr, Nd, Pb and other REEs to get the most information out of small (5-10 mg) dust samples recovered from ice cores. Although Hf isotopes have recently been added as a robust tool of aerosol/dust source discrimination (e.g. [4,5,6,7]), precise Hf isotopic measurements of small (Central Europe (NUS), China (BEI) and the US (JUD) were processed (all acetic acid treated for carbonate removal, i.e. aluminosilicate fractions were analysed). Sr isotopic compositions varied between the aliquots within a range of ˜0.00007 for the three samples. Comparison of these values with previously obtained 87Sr/86Sr isotopic ratios from the same samples (different acid/sample amounts) reveals that these values are very sensitive to the acetic acid treatment (acid

  18. Zinc isotopic compositions of breast cancer tissue. (United States)

    Larner, Fiona; Woodley, Laura N; Shousha, Sami; Moyes, Ashley; Humphreys-Williams, Emma; Strekopytov, Stanislav; Halliday, Alex N; Rehkämper, Mark; Coombes, R Charles


    An early diagnostic biomarker for breast cancer is essential to improve outcome. High precision isotopic analysis, originating in Earth sciences, can detect very small shifts in metal pathways. For the first time, the natural intrinsic Zn isotopic compositions of various tissues in breast cancer patients and controls were determined. Breast cancer tumours were found to have a significantly lighter Zn isotopic composition than the blood, serum and healthy breast tissue in both groups. The Zn isotopic lightness in tumours suggests that sulphur rich metallothionein dominates the isotopic selectivity of a breast tissue cell, rather than Zn-specific proteins. This reveals a possible mechanism of Zn delivery to Zn-sequestering vesicles by metallothionein, and is supported by a similar signature observed in the copper isotopic compositions of one breast cancer patient. This change in intrinsic isotopic compositions due to cancer has the potential to provide a novel early biomarker for breast cancer.

  19. Evidence for Slab Melt Contributions to the Mexican Volcanic Belt and Other Young Hot Slab Arcs from Lu-Hf Isotopes (United States)

    Goldstein, S. L.; Cai, Y. M.; Langmuir, C. H.; Lagatta, A.; Straub, S. M.; Gomez-Tuena, A.; Martin Del Pozzo, A.


    Despite major advances in delineating the processes that govern magma generation at convergent margins, the problem persists of distinguishing slab, mantle wedge, and crustal contributions. A corrollary question is whether there is significant melting of subducted ocean crust. Especially in thick crust regions, the importance of crustal versus mantle contributions to lavas represents a long-standing fundamental issue in arc magma geochemistry. We show that frontal arc magmas from the Central Mexican Volcanic Belt (CMVB), including the large andesitic stratovolcanoes Popocatepetl and Nevado de Toluca, display negligible crustal contamination, and contain substantial contributions from melting of subducted Pacific ocean crust. Despite ca. 50 km thick continental crust, the CMVB erupts near primitive lavas including "high-Nb" alkaline basalts that show negligible "subduction signatures" in their trace element patterns. These "high-Nb" basalts define the regional mantle wedge composition in isotope-trace element space. The "normal" calcalkaline lavas form a negative correlation between Hf isotopes and Lu/Hf. One endmember is like the high Nb basalts representing the regional mantle wedge. The other endmember has higher Hf isotopes (approaching values of Pacific MORB) and very low Lu/Hf of less than 0.04 (e.g. compared to typical values of ca. 0.2 in Pacific MORB). The low Lu/Hf values require low degree partial melting of a source rich in garnet. The high Hf isotopes require a depleted mantle source with isotopes like Pacific MORB. Together the Lu-Hf data indicate a substantial component derived from melting of eclogitic Pacific ocean crust. A key feature of the data is that the stratovolcano lavas showing the largest slab melt signature also show the highest Hf isotope ratios and thus are more "depleted mantle-like" than the regional mantle wedge. Thus, the integrated data allow us to clearly distinguish between mantle and crustal sources in the CMVB and point to

  20. Timing and origin of migmatitic gneisses in south Karakoram: Insights from U-Pb, Hf and O isotopic record of zircons (United States)

    Mahar, Munazzam Ali; Mahéo, Gweltaz; Goodell, Philip C.; Pavlis, Terry L.


    The timing and origin of partial melting in collision belts is crucial to understand the thermotectonic evolution and the relationship between HT metamorphism and magmatism in over-thickened crust. In the present study, we used the in-situ isotopic (Hf, O and U-Pb) record of zircons to investigate the timing and origin of migmatitic gneisses exposed in the core of the Dassu dome in south Karakoram. The new U-Pb zircon dating identified the Proterozoic inherited cores (1.8-1.9 Ga and 2.3-2.5 Ga) surrounded by a Neogene overgrowth with ages ranging from ∼6 to ∼20 Ma. These ages imply that the partial melting in the Karakoram Metamorphic Complex lasted from >20 Ma to ∼6 Ma and can be correlated with the Miocene magmatism in the adjacent Baltoro region. Oxygen isotopic data from Proterozoic inherited cores (1.8-1.9 Ga) and Neogene overgrowths are indistinguishable and generally vary from 8‰ to 9.5‰. These values are slightly higher than the most igneous zircons (6.5-8‰, Valley et al., 2005) indicating an igneous precursor with heavy initial O composition that later might have equilibrated with low temperature environment or some involvement of supracrustal material is likely. However, a few low U/Th, relatively old inherited cores (2.3-2.5 Ga) showed mantle-like (δ18O = 5.3 ± 0.6‰, Valley et al., 2005) values of δ18O = 5.5 ± 2.7‰. The present-day weighted mean εHf (0) of the Proterozoic inherited cores ranges from -50 ± 1.0 to -44.3 ± 1.2. In contrast, the Neogene rims are 15-20 ε-units higher than the inherited core with present-day εHf (0) = -30.6 ± 0.9. This implies that the Hf composition of the Neogene overgrowth is not controlled exclusively by the dissolution of the inherited cores and that contamination by external melts is likely. We suggest a contribution from the Neogene, less-evolved magmatism in the Baltoro region (εHf (0) = ∼-4 to -10). The elevated oxygen composition is not consistent with the contribution from pristine

  1. Sr, Nd, Pb and Hf isotopic constraints on mantle sources and crustal contaminants in the Payenia volcanic province, Argentina

    DEFF Research Database (Denmark)

    Søager, Nina; Holm, Paul Martin; Thirlwall, Matthew F.


    The presented Sr, Nd, Hf and double-spike Pb-isotopic analyses of Quaternary basalts from the Payenia volcanic province in southern Mendoza, Argentina, confirm the presence of two distinct mantle types feeding the Payenia volcanism. The southern Payenia mantle source feeding the intraplate-type Río...... is suggested to be caused by step-wise melt extraction due to repeated injections of subduction zone fluids and melts. The lower crustal contamination trends found in the trace element variations of basalt groups from all parts of the Payenia province are also recognized in isotopic space and the dominant...... isotope assimilation trends indicate lower crustal contaminants with more unradiogenic Pb, lower 143Nd/144Nd and 176Hf/177Hf and higher or similar 87Sr/86Sr as the mantle melts. These characteristics are similar to those found in lower crustal xenoliths from the northern Proterozoic Cuyania terrane...

  2. Coupled zircon Lu-Hf and U-Pb isotopic analyses of the oldest terrestrial crust, the >4.03 Ga Acasta Gneiss Complex (United States)

    Bauer, Ann M.; Fisher, Christopher M.; Vervoort, Jeffrey D.; Bowring, Samuel A.


    The Acasta Gneiss Complex of the Northwest Territories, Canada, contains some of the earliest terrestrial continental crust and thus provides a critical sample set for characterization of crust-forming processes on the early Earth. Here we report the results of a combined Lu-Hf and U-Pb isotopic study of zircons from predominantly felsic orthogneisses from the Acasta Gneiss Complex that crystallized between ∼4.0 and 2.9 Ga, many of which contain complex zoning and therefore require an analytical treatment suited to distinguish amongst compositionally distinct age and Hf isotopic domains. To ensure the reliability of the analyses and of subsequent geologic interpretations, we employed the laser ablation split-stream (LASS) technique to concurrently measure the Lu-Hf and U-Pb isotopic systems in zircon. Our results confirm prior findings of precursor Hadean crust (>4.0 Ga) in the source of these rocks and the continued involvement of this reservoir until ∼3.6 Ga. We present evidence for the input of relatively more juvenile material at ∼3.6 Ga, which we suggest corresponds to a fundamental change in the source of the magmas. This study extends the lower bound of the published Acasta Hf isotopic record from 3.6 Ga to 2.9 Ga and demonstrates that the ∼3.6 Ga-2.9 Ga interval is largely represented by reworking of relatively juvenile ∼3.6 Ga crust and the diminution of the >4.0 Ga crustal signal. Significantly, there is no evidence that rocks within the Acasta Gneiss Complex were derived from a strongly depleted mantle.

  3. A convergent continent marginal volcanism source of ash beds near the Permian-Triassic boundary, South China: Constraints from trace elements and Hf-isotopes (United States)

    Wang, X.; Zhao, L.; Chen, Z. Q.; Ma, D.; Yan, P.; Guo, F.; Wang, F.; Wan, Q.; Han, X.


    Growing evidence shows that volcanism near the Permian-Triassic boundary (PTB) may have been crucial in triggering the PTB biocrisis. However, whether this trigger is the Siberian traps or arc island volcanisms has long been debating. Meanwhile, multiple claystone beds are prominent near the PTB, South China. The nature and origin of the volcanic ashes therefore provide clue to find out the trigger of the PTB mass extinction. Following previous studies (Gao et al., 2013), 21 PTB ash beds from three additional PTB sections, namely the Shangsi, Jianshi and Meishan, all from South China have been systematically sampled. The U-Pb ages, trace elements, and Hf-isotope compositions of zircon grains from these ash beds were analyzed using LA-ICPMS and LA-MC-ICPMS. Volcanic ash geochemistry shows presence of Rhyolite or Dacite and reveal a collision-tectonic setting. Zircons from these ash layers yield comparatively low Nb/Hf and high Th/Nb ratios, dropping into the range of arc/orogenic-related settings. Zircon Hf-isotope compositions show that ɛHf(t) values vary from -11.7 to 1.8, indicating that at least two kinds of crustal component have been involved: juvenile lower crust and ancient middle-upper crust. The ash beds (Ss27a, Js129, Js130, Ms25, Ms26) near biotic extinction horizon have significant larger variation range of ɛHf(t) and relatively positive averages, implying that more juvenile lower crustal material had contributed to the volcanisms. This means that these volcanisms may have originated deeper depth or the volcanisms erupted so rapidly that there was no enough time for the mixing of different components. The volcanisms associated with biotic extinction should be the most intense and have greatest heat put. Spatial and temporal distributions of ash beds from thirty PTB sections worldwide reveal that the PTB volcanic ashes occurred only in the Paleo-Tethys region, suggesting that the volcanisms may be likely limited to the Paleo-Tethys continental

  4. Combined U-Pb and Lu-Hf isotope analyses by laser ablation MC-ICP-MS: methodology and applications

    Energy Technology Data Exchange (ETDEWEB)

    Matteini, Massimo; Dantas, Elton L.; Pimentel, Marcio M.; Bühn, Bernhard, E-mail: [Universidade de Brasilia (UnB), DF (Brazil). Instituto de Geociencias


    The Lutetium-Hafnium isotopic system represents one of the most innovative and powerful tools for geochronology and isotopic studies. Combined U-Pb and Lu-Hf in situ analyses on zircon by LA-MC-ICP-MS permit to characterize isotopically the host magma from which it crystallized furnishing significant information for sediment provenance and crustal evolution studies. In this paper e describe the Lu-Hf systematic by LA-MC-ICP-MS developed in the laboratory of Geochronology of the University of Brasilia and report the results obtained by repeated analyses of {sup 176}Hf/{sup 177}Hf isotopic ratio of three zircon standards: GJ-1 = 0.282022 ± 11 (n=56), Temora 2 = 0.282693 ± 14 (n=25) and UQZ = 0.282127 ± 33 (n=11). The {sup 176}Hf/{sup 177}Hf ratio (0.282352 ± 22, n=14) of gem quality zircon used as in-house standard have been also characterized. As a geological application, we analyzed two complex zircons selected from a migmatitic rocks from the Borborema Province, NE Brazil. On the basis of U-Pb and Lu-Hf data, two main crystallization events have been identified in both studied zircons. An older event at ca. 2.05 Ga recognized in the inherited cores represents a well-characterized paleoproterozoic magmatic event that affected the whole Borborema Province. A second crystallization event at ∼ 575 Ma, recognized at the rims, represents a Neoproterozoic (Brazilian) high grade metamorphic-magmatic event. (author)

  5. U-Pb ases and Hf isotopes for detrital zircons from quartzite in the Paleoproterozoic Songshan Group on the southwestern margin of the North China Craton

    Institute of Scientific and Technical Information of China (English)

    DIWU ChunRong; SUN Yong; YUAN HongLin; WANG HongLiang; ZHONG XingPing; LIU XiaoMing


    In situ U-Pb dating and Lu-Hf isotopic analysis were carried out for detrital zircons from quartzite in the Paleoproterozoic Songshan Group on the southern margin of the North China Craton (NCC). The re-sults provide further constraints on the crustal formation and evolution history of NCC. Four 207Pb/206Pb age populations were obtained from 99 analyses, with clusters at ~3.40 Ga, 2.77-2.80 Ga, ~2.50 Ga and 2.34 Ga, respectively. The 3.40 Ga old zircons have similar Hf isotopic compositions to those from Ar-chean rocks in the Jidong and Anshan areas of NCC. However, crustal remnants older than 3.6 Ga have been identified in the southern margin of NCC, the South China Craton, the northwestern part of the Qinling Orogen and its adjacent area. Thus, it is not easy to trace the source rock from which the 3.40 Ga detrital zircons were derived. It can be inferred that the crustal remnants older than 3.40 Ga might have been widely distributed in the North China Craton. The 2.77-2.80 Ga zircons make up a relatively small proportion and have the highest ε (t) values (up to 6.1±1.6), consistent with the Hf isotopic composition of the depleted mantle at 2.83 Ga. Their single-stage Hf model age of 2.83 Ga is close to their crystallized age, suggesting that their source rocks were extracted from the contemporaneous depleted mantle. The ~2.50 Ga zircon grains constitute about 85% of the total grain population and their Hf isotopic compositions indicate major growth of juvenile crust at ~2.50 Ga but minor reworking of ancient crust. The youngest zircon dated in this study gave an U-Pb age of 2337±23 Ma, which can be considered the maximum depositional age of the formation of the Songshan Group.

  6. Zircon U-Pb ages and Hf-O isotope compositions of the Zhaheba ophiolite in the northern margin of the Junggar terrane and their tectonic implications%扎河坝蛇绿岩锆石U-Pb年龄、Hf-O同位素组成及其地质意义

    Institute of Scientific and Technical Information of China (English)

    潘成泽; 邱林; 叶现韬; 董永观


    扎河坝蛇绿岩位于准噶尔北缘,是扎河坝—阿尔曼太蛇绿混杂岩带的一部分.通过对蛇绿混杂岩中堆晶辉长岩和凝灰岩夹层的锆石U-Pb年龄及Hf-O同位素进行研究,获得堆晶辉长岩的结晶年龄为485±4Ma,凝灰岩的喷发年龄为401±2.5Ma.辉长岩极度亏损Hf同位素,εHf (t)为13~20,δ18O峰值为+5.37‰,显示其具有地幔特征.凝灰岩锆石的Hf同位素亏损程度低于堆晶辉长岩,εHf (t)为1.4~9.2.扎河坝蛇绿岩具有典型的SSZ型蛇绿岩特征,是通过俯冲增生到洋内弧弧前的蛇绿岩.

  7. The effects of composition on mechanical properties of W-4Re-Hf-C alloys (United States)

    Witzke, W. R.


    Studies were made of the effects of alloy composition on the mechanical behavior of as-worked W-4Re-Hf-C alloys containing up to about 0.8 mol % Hfc. Extracted second-phase particles were analyzed and related to alloy composition and creep strength. While strengthening is attributed to HfC particles, the presence of excess hafnium or carbon (above the calculated amounts for stoichiometric HfC) in swaged W-4Re-Hf-C alloys generally causes a reduction of the high-temperature (1930 C) tensile strength; maximum creep strength is, however, indicated for alloys with a slight (about 0.05 to 0.1 at. %) excess of hafnium. Particle strengthening is reduced by WC in solid solution with HfC for allow compositions with an excess of carbon. The low-temperature ductility of worked W-4Re-Hf-C alloys appears to be far more dependent on the amount of excess C or Hf present than on the HfC particle content in the range studies.

  8. Zircon U-Pb age and Hf isotope of Quanyishang A-type granite in Yichang: Signification for the Yangtze continental cratonization in Paleoproterozoic

    Institute of Scientific and Technical Information of China (English)

    XIONG Qing; ZHENG JianPing; YU ChunMei; SU YuPing; TANG HuaYun; ZHANG ZhiHai


    Zircon U-Pb age and Hf isotope, and major and trace element compositions were reported for granite at Quanyishang, which intruded into the Kongling complex in Yichang, Hubei Province. The results show that the Quanyishang granite is rich in silicon and alkalis but poor in calcium and magnesium, and displays enrichment in Ga, Y, Zr, Nb but depletion in Sr and Ba, exhibiting the post-orogenic A-type affinity. 90% zircons from the granite are concordant, and give a middle Paleoproterozoic magmatic crystallization age (mean 1854 Ma). Initial Hf isotope ratios (176Hf/177Hf)1 of the middle Paleoproterozoic zircons range from 0.280863 to 0.281134 and they have negative εHf(t) values with a minimum of -26.3. These zircons give the depleted mantle model ages (TDM) of 2.9-3.3 Ga (mean 3.0 Ga), and the average crustal model ages (Tcrust) of 3.6-4.2 Ga (mean 3.8 Ga)., A Mesoarchean grain with 207pb/206Pb age of 2859 Ma has a slightly high TDM (3.4 Ga) but similar Tcrust (3.8 Ga) to the Paleoproterozoic zircons. All these data suggest that the source materials of the Quanyishang A-type granite are unusually old, at least ≥2.9 Ga (even Eoarchean). The event of crustal remelting, which resulted in the formation of the Quanyishang granite in the middle Paleoproterozoic, recorded the cratonization of the Yangtze conti-nent. The process may have relation to the extension and collapse of the deep crust with Archean ages, in response to the transition stage of the assembly and breakup of the Columbia supercontinent.

  9. Collective structural evolution in neutron-rich Yb, Hf, W, Os and Pt isotopes

    CERN Document Server

    Nomura, K; Rodriguez-Guzman, R; Robledo, L M; Sarriguren, P


    The low-lying quadrupole collective states in neutron-rich even-even Yb, Hf, W, Os, and Pt isotopes are studied in a systematic way. Spectroscopic calculations are performed in terms of the Interacting Boson Model Hamiltonian, which is determined from the Hartree-Fock-Bogoliubov (HFB) approach with Gogny Energy Density Functionals (EDFs). The multi-fermion dynamics of the surface deformation is simulated by the bosonic degrees of freedom so that the potential energy surface (PES) with quadrupole degrees of freedom, obtained from the constrained HFB calculations, is mapped onto the corresponding PES of the IBM system. The interaction strengths of the proton-neutron IBM (IBM-2) Hamiltonian are determined through this procedure, which enables one to access the spectroscopic properties. We demonstrate the occurrence of a prolate-to-oblate shape/phase transition as a function of neutron number in the considered isotope chains in both HFB (with D1S and D1M EDFs) and the corresponding mapped IBM PESs. The shape tran...

  10. In-situ zircon U-Pb age and Hf-O isotopic constraints on the origin of the Hasan-Robat A-type granite from Sanandaj-Sirjan zone, Iran: implications for reworking of Cadomian arc igneous rocks (United States)

    Honarmand, Maryam; Li, Xian-Hua; Nabatian, Ghasem; Neubauer, Franz


    The Lower Permian Hasan-Robat syenogranite occurs as a single pluton and intruded the Upper Carboniferous-Lower Permian sandstones and dolomitic limestones in the central part of the Sanandaj-Sirjan zone. This syenogranitic intrusion shows A-type granitic affinity and is a good representative of Early Permian igneous activity in Iran. SIMS U-Pb zircon analyses indicate a crystallization age of 294.2 ± 2.5 Ma for the Hasan-Robat A-type granite. In-situ Lu-Hf and oxygen isotope analyses of magmatic zircons were carried out to infer the magma sources and evolution of the Hasan-Robat A-type syenogranite. The Hf-O zircon isotopic compositions are relatively homogeneous, with nearly chondritic ɛHf(t) values of -0.8 to +2.4 corresponding to two-stage zircon Hf model ages of 1.15-1.36 Ga. The δ18O values of zircon range from +7.6 to +8.6‰. The Hf model ages of the Hasan-Robat zircons is within the range of those reported from the Cadomian granitoids in Iran. The isotopic features of the Hasan-Robat syenogranite are in good agreement with Hf isotopic values and Hf and Nd model ages reported from the Cadomian arc magmatic suites in Iran. Thus, partial melting of these Cadomian igneous rocks would be the favorite source for the Hasan-Robat syenogranitic magma during the opening of the Neotethys Ocean and separation of Iranian terranes from the northern margin of Gondwana.

  11. Nickel isotopic composition of the mantle (United States)

    Gall, Louise; Williams, Helen M.; Halliday, Alex N.; Kerr, Andrew C.


    This paper presents a detailed high-precision study of Ni isotope variations in mantle peridotites and their minerals, komatiites as well as chondritic and iron meteorites. Ultramafic rocks display a relatively large range in δ60 Ni (permil deviation in 60 Ni /58 Ni relative to the NIST SRM 986 Ni isotope standard) for this environment, from 0.15 ± 0.07‰ to 0.36 ± 0.08‰, with olivine-rich rocks such as dunite and olivine cumulates showing lighter isotope compositions than komatiite, lherzolite and pyroxenite samples. The data for the mineral separates shed light on the origin of these variations. Olivine and orthopyroxene display light δ60 Ni whereas clinopyroxene and garnet are isotopically heavy. This indicates that peridotite whole-rock δ60 Ni may be controlled by variations in modal mineralogy, with the prediction that mantle melts will display variable δ60 Ni values due to variations in residual mantle and cumulate mineralogy. Based on fertile peridotite xenoliths and Phanerozoic komatiite samples it is concluded that the upper mantle has a relatively homogeneous Ni isotope composition, with the best estimate of δ60Nimantle being 0.23 ± 0.06‰ (2 s.d.). Given that >99% of the Ni in the silicate Earth is located in the mantle, this also defines the Ni isotope composition of the Bulk Silicate Earth (BSE). This value is nearly identical to the results obtained for a suite of chondrites and iron meteorites (mean δ60 Ni 0.26 ± 0.12‰ and 0.29 ± 0.10‰, respectively) showing that the BSE is chondritic with respect to its Ni isotope composition, with little to no Ni mass-dependent isotope fractionation resulting from core formation.

  12. Comparative behavior of Sr, Nd and Hf isotopic systems during fluid-related deformation at middle crust levels (United States)

    Luais, Béatrice; Le Carlier de Veslud, Christian; Géraud, Yves; Gauthier-Lafaye, François


    We have carried out a comparative Rb-Sr, Sm-Nd and Lu-Hf isotopic study of a progressively deformed hercynian leucogranite from the French Massif Central, belonging to the La Marche ductile shear zone, in order to investigate the respective perturbation of these geochronometers with fluid induced deformation. The one-meter wide outcrop presents a strongly deformed and mylonitized zone at the center, and an asymmetric deformation pattern with a higher deformation gradient on the northern side of the zone. Ten samples have been carefully collected every 10 cm North and South away from the strongest deformed mylonitic zone. They have been analyzed for a complete major, trace element data set, oxygen isotopes, Rb-Sr, Sm-Nd and Lu-Hf isotopic systematics. We show that most of major and trace elements except SiO 2, alkaline elements (K 2O, Rb), and some metal transition elements (Cu), are progressively depleted with increasing deformation. This depletion includes REE + Y, but also HFS elements (Ti, Hf, Zr, Nb) which are commonly considered as immobile elements during upper level processes. Variations in elemental ratios with deformation, e.g. decrease in LREE/MREE- HREE, Nd/Hf, Th/Sr, increase in Rb/Sr, U/Th and constant Sr/Nd, lead to propose the following order of element mobility: U ≫ Th > Sr = Nd ≫ Hf + HREE. We conclude in agreement with previous tectonic and metallogenic studies that trace element patterns across the shear zone result from circulation of oxidizing F-rich hydrothermal fluids associated with deformation. A temperature of the fluid of 470-480 °C can be deduced from the δ 18O equilibrium between quartz-muscovite pairs. Elemental fractionation induces perturbation of the Rb-Sr geochronometer. The well-defined 87Rb/ 86Sr- 87Sr/ 86Sr correlation gives an apparent age of 294 ± 19 Ma, slightly younger than the 323 ± 4 Ma age of leucogranites in this area. This apparent age is interpreted as dating event of intense deformation and fluid circulation

  13. U-Pb zircon geochronology and Nd-Hf-O isotopic systematics of the Neoproterozoic Hadb adh Dayheen ring complex, Central Arabian Shield, Saudi Arabia (United States)

    Ali, Kamal A.; Jeon, Heejin; Andresen, Arild; Li, Shuang-Qing; Harbi, Hesham M.; Hegner, Ernst


    A combined study of single zircon U-Pb dating, Hf-O zircon isotopic analyses and whole-rock Nd isotopic compositions was carried out to infer the magma sources of Neoproterozoic post-collisional A-type granitoids in Saudi Arabia. U-Pb zircon dating of magmatic zircons of two samples from the Hadb adh Dayheen ring complex yielded ages of 625 ± 11 Ma for a hornblende-biotite granite sample, and 613 ± 4 Ma for a monzogranite sample. The granitic rocks show initial εNd values of + 4.1 to + 5.3 and εHf of + 4.5 to + 8.4 that are lower than those of a model depleted mantle (εHf ~+ 14 and εNd ~+ 6.5) and consistent with melting of subduction-related crustal protoliths that were formed during the Neoproterozoic assembly of the Arabian-Nubian Shield (ANS). Crustal-model ages (Hf-tNC) of 0.81 to 1.1 Ga are inconsistent with depleted-mantle Nd model ages of 0.71 to 0.81 Ga and indicate that the post-collisional Hadb adh Dayheen granites were derived mostly from juvenile crust formed in Neoproterozoic time. Single zircons data show a wide range in δ18O values from + 3.2‰ to + 6.4‰, possibly indicating crystallization of zircon from magma derived from magmatic rocks altered by meteoric water in a magma chamber-caldera system.

  14. Archean crustal evolution in the Southern São Francisco craton, Brazil: Constraints from U-Pb, Lu-Hf and O isotope analyses (United States)

    Albert, Capucine; Farina, Federico; Lana, Cristiano; Stevens, Gary; Storey, Craig; Gerdes, Axel; Dopico, Carmen Martínez


    In this study we present U-Pb and Hf isotope data combined with O isotopes in zircon from Neoarchean granitoids and gneisses of the southern São Francisco craton in Brazil. The basement rocks record three distinct magmatic events: Rio das Velhas I (2920-2850 Ma), Rio das Velhas II (2800-2760 Ma) and Mamona (2750-2680 Ma). The three sampled metamorphic complexes (Bação, Bonfim and Belo Horizonte) have distinct εHf vs. time arrays, indicating that they grew as separate terranes. Paleoarchean crust is identified as a source which has been incorporated into younger magmatic rocks via melting and mixing with younger juvenile material, assimilation and/or source contamination processes. The continental crust in the southern São Francisco craton underwent a change in magmatic composition from medium- to high-K granitoids in the latest stages, indicating a progressive HFSE enrichment of the sources that underwent anatexis in the different stages and possibly shallowing of the melting depth. Oxygen isotope data shows a secular trend towards high δ18O (up to 7.79‰) indicating the involvement of metasediments in the petrogenesis of the high potassium granitoids during the Mamona event. In addition, low δ18O values (down to 2.50‰) throughout the Meso- and Neoarchean emphasize the importance of meteoritic fluids in intra-crustal magmatism. We used hafnium isotope modelling from a compilation of detrital zircon compositions to constrain crustal growth rates and geodynamics from 3.50 to 2.65 Ga. The modelling points to a change in geodynamic process in the southern São Francisco craton at 2.9 Ga, from a regime dominated by net crustal growth in the Paleoarchean to a Neoarchean regime marked by crustal reworking. The reworking processes account for the wide variety of granitoid magmatism and are attributed to the onset of continental collision.

  15. Laser Ablation Split Stream (LASS) U-Pb & Lu-Hf Isotope Analysis of Detrital Zircons from the Old Red Sandstone, NW Svalbard: Implications for Northern Caledonian Paleogeography (United States)

    Beranek, L. P.; Gee, D. G.; Fisher, C. M.


    The Svalbard archipelago consists of three Caledonian provinces that were assembled by thrusting and transcurrent faulting during the Silurian and Devonian in a location directly northeast of the Greenland Caledonides. Syn- to post-orogenic alluvial strata, referred to as the Old Red Sandstones, filled pull-apart basins adjacent to the transcurrent faults and comprise cover assemblages that help constrain the timing of the Caledonian orogeny. To further investigate the tectonic history and paleogeography of the Raudfjorden-Liefdefjorden-Woodfjorden area of Spitsbergen, NW Svalbard, we analyzed rock samples of the Old Red Sandstones and underlying Precambrian basement complexes for detrital zircon analysis. Laboratory studies of the Old Red Sandstones include the novel Laser Ablation Split Stream (LASS) technique, which allows for simultaneous U-Pb & Lu-Hf isotope analysis of zircon crystals. Lower Devonian Red Bay Group strata contain a range of early Neoproterozoic to Neoarchean detrital zircons with prominent age peaks c. 960, 1050, 1370, 1450, 1650, and 2700 Ma; subordinate Ordovician (c. 460-490 Ma) and Cryogenian (c. 650 Ma) detrital zircons occur in a subset of the samples. Underlying Precambrian metasedimentary rocks are composed of similar earliest Neoproterozoic to Neoarchean age populations, which argues for much of the Red Bay Group to be derived from local basement rocks during thrusting and other faulting. The U-Pb ages and Hf isotope compositions of Paleozoic to Neoarchean detrital zircons are consistent with Arctic crustal evolution, and support the hypothesis that northwestern and northeastern provinces of the Svalbard Caledonides are extruded fragments of the northeast Greenland allochthons. The new Hf isotope results further allow paleogeographic and stratigraphic comparisons with rock assemblages proximal to the North Atlantic Caledonides during the Silurian-Devonian, including the Pearya terrane of Ellesmere Island, Alexander terrane of NW

  16. Combined U-Pb and Lu-Hf isotope analyses by laser ablation MC-ICP-MS: methodology and applications

    Directory of Open Access Journals (Sweden)

    Massimo Matteini


    Full Text Available The Lutetium-Hafnium isotopic system represents one of the most innovative and powerful tools for geochronology and isotopic studies. Combined U-Pb and Lu-Hf in situ analyses on zircon by LA-MC-ICP-MS permit to characterize isotopically the host magma from which it crystallized furnishing significant information for sediment provenance and crustal evolution studies. In this paper e describe the Lu-Hf systematic by LA-MC-ICP-MS developed in the laboratory of Geochronology of the University of Brasilia and report the results obtained by repeated analyses of 176Hf/177Hf isotopic ratio of three zircon standards: GJ-1 = 0.282022 ± 11 (n=56, Temora 2 = 0.282693 ± 14 (n=25 and UQZ = 0.282127 ± 33 (n=11. The 176Hf/177Hf ratio (0.282352 ± 22, n=14 of gem quality zircon used as in-house standard have been also characterized. As a geological application, we analyzed two complex zircons selected from a migmatitic rocks from the Borborema Province, NE Brazil. On the basis of U-Pb and Lu-Hf data, two main crystallization events have been identified in both studied zircons. An older event at ca. 2.05 Ga recognized in the inherited cores represents a well-characterized paleoproterozoic magmatic event that affected the whole Borborema Province. A second crystallization event at ~ 575 Ma, recognized at the rims, represents a Neoproterozoic (Brazilian high grade metamorphic-magmatic event.O sistema isotópico Lutécio-Hafnio representa uma das ferramentas mais recentes e poderosas para estudos isotópicos e geocronológicos. Análises combinadas in situ de U-Pb e Lu-Hf sobre zircão pelo LA-MC-ICP-MS permitem caracterizar iso-topicamente o magma onde ele cristalizou, fornecendo valiosas informações para estudos de proveniência de sedimento e de evolução crustal. Nesse trabalho descrevemos a sistemática de Lu-Hf pelo LA-MC-ICP-MS implantada no laboratório de Geocronologia da Universidade de Brasília e reportamos os resultados obtidos de repetidas an

  17. Geochronology, geochemistry, and Sr-Nd-Hf isotopes of the early Paleozoic igneous rocks in the Duobaoshan area, NE China, and their geological significance (United States)

    Wu, Guang; Chen, Yuchuan; Sun, Fengyue; Liu, Jun; Wang, Guorui; Xu, Bei


    The Duobaoshan area of northwestern Heilongjiang Province is the most important copper resource concentration region in NE China. To date, the Duobaoshan superlarge Cu-Mo deposit and the Tongshan large Cu-Mo deposit have been discovered in the Duobaoshan area. Both the deposits are hosted by granodiorites and volcanic rocks. Zircon LA-ICP-MS U-Pb dating indicates that these granodiorites emplaced approximately 479 Ma ago and that those volcanic rocks erupted between 447 and 450 Ma. The early Ordovicain granodiorites belong to the high-K to medium-K calc-alkaline series and are characterized by high Al2O3 and Sr contents, low Yb and Y contents, and relatively low Mg# values and Na2O/K2O ratios, with positive Eu or slight negative Eu anomalies (averaging 1.18). All of these geochemical characters are similar to those of the adakites generated by partial melting of a thickened lower crust in the world. Moreover, the granodiorites have low initial 87Sr/86Sr ratios (varying from 0.703474 to 0.704436), very high zircon εHf(t) and whole-rock εNd(t) values (varying from 13.0 to 16.8 and 5.27 to 5.46, respectively), and young zircon Hf and whole-rock Nd single-stage and two-stage model ages. Taking these geochemical characteristics and Sr-Nd-Hf isotope compositions together, we suggest that the early Ordovician granodiorites in the Duobaoshan area occurred in a post-collision environment and were formed by partial melting of a juvenile thickened lower crust dominated by depleted mantle-derived material. These late Ordovician volcanic rocks, which are composed of basalt, basaltic andesite, and andesite, belong to the tholeiitic or calc-alkaline series. They are generally enriched in large ion lithophile elements (LILEs) and depleted in high field strength elements (HFSEs; e.g., Nb, Ta, Zr, Hf, P, and Ti), consistent with the geochemistry of igneous rocks from island arcs or active continental margins. Compared with the early Ordovician granodiorites, these volcanic rocks

  18. Petrogenesis of the igneous Mucajaí AMG complex, northern Amazonian craton — Geochemical, U-Pb geochronological, and Nd-Hf-O isotopic constraints (United States)

    Heinonen, A. P.; Fraga, L. M.; Rämö, O. T.; Dall'Agnol, R.; Mänttäri, I.; Andersen, T.


    The ca. 1525 Ma igneous Mucajaí anorthosite-monzonite-granite (AMG) complex in northern Brazil is a rare manifestation of Mesoproterozoic intraplate magmatism in the northern Amazonian Craton. The complex comprises a two-phase rapakivi granite batholith with subordinate quartz-fayalite monzonites and syenites and the closely associated Repartimento anorthosite. Zircon U-Pb (ID-TIMS) geochronology reveals that the anorthosite (1526 ± 2 Ma), monzonite (1526 ± 2 Ma), and the main-phase biotite-hornblende granite (1527 ± 2 Ma) of the complex intruded the Paleoproterozoic (~ 1.94 Ga) country rocks simultaneously at ~ 1526 Ma and that the more evolved biotite granite is marginally younger at 1519 ± 2 Ma. Intraplate magmatism in the Mucajaí region was relatively short-lived and lasted 12 million years (1529-1517 Ma) at maximum. The Nd (whole-rock, ID-TIMS; ɛNd from - 1.9 to - 2.8), Hf (zircon, LAM-ICP-MS; ɛHf from - 2.0 to - 3.1), and O (zircon, SIMS; δ18O from 6.1 to 7.0‰) isotopic compositions of the studied rocks are fairly uniform but still reveal a small degree of isotopic heterogeneity in the Paleoproterozoic crust enclosing the complex. The small isotopic differences observed in the two types of rapakivi granites (biotite-hornblende granite and biotite granite) may result either from an isotopically heterogeneous lower crustal source or, more likely, from contamination of the granitic magma derived from a lower crustal source during prolonged residence at upper crustal levels.

  19. Hf and Nd Isotope Evidence for Production of an Incompatible Trace Element Enriched Crustal Reservoir in Early Earth (Invited) (United States)

    Brandon, A. D.; Debaille, V.; Lapen, T. J.


    The final significant stage of accretion of the Earth was likely a collision between proto-Earth and a Mars sized impactor that formed the Moon. This event is thought to have produced enough thermal energy to melt all or most of the Earth, with a consequent magma ocean (MO). During subsequent cooling, the Earth would have formed its protocrust and corresponding mantle lithosphere, consisting of solidified basalt-komatiitic melt, in combination with buoyant cumulates and late stage residual melts from the MO. Relative to the convecting mantle, portions of this protolithosphere are likely to have been enriched in incompatible trace elements (ITE) in sufficient quantities to contain a significant amount of the bulk Earth’s budget for rare earth elements, U, Th, and Hf. If the protolithosphere was negatively buoyant, it may have overturned at or near the final stages of MO crystallization and a significant portion of that material may have been transported into the deep mantle where it resided and remixed into the convecting mantle over Earth history [1,2]. If the protolithosphere remained positively buoyant, its crust would have likely begun to erode from surface processes, and subsequently recycled back into the mantle over time as sediment and altered crust, once a subduction mechanism arose. The Nd and Hf isotopic compositions of Earth’s earliest rocks support the idea that an early-formed ITE-enriched reservoir was produced. The maxima in 142Nd/144Nd for 3.85 to 3.64 Ga rocks from Isua, Greenland decreases from +20 ppm to +12 ppm relative to the present day mantle value, respectively [3]. This indicates mixing of an early-formed ITE enriched reservoir back into the convecting mantle. In addition, zircons from the 3.1 Ga Jack Hills conglomerate indicate that material with an enriched 176Lu/177Hf of ~0.02 and an age of 4.4 Ga or greater was present at the Earth’s surface over the first 2 Ga of Earth history, supporting the scenario of a positively buoyant

  20. Efficacy of Experimental Hydrofluoric Acid (HF on Bond Strength and Microleakage of Composite-Porcelain Interface

    Directory of Open Access Journals (Sweden)

    Samaneh Mahvidyzadeh


    Full Text Available Background and Aims: The aim of this study was to evaluate the quality of an experimental hydrofluoric acid (HF for preparation of porcelain and to compare it with two commercial hydrofluoric acids in Iranian trademark. Materials and Methods: A- Evaluation of etch pattern of experimental HF using scanning electron microscope (SEM: 6 feldespathic discs were divided into 3 groups. Each group was etched with related HF (experimental, Ultradent and Kimia for 1 minute. SEM images were recorded at 3 magnifications. B- Bond strength test: 18 feldespathic discs were considered for each acidic group. Then the porcelain surfaces were etched and bonded to composite with unfilled resin. Consequently, the microshear test was done. C- Microleakage test: 54 discs were divided into 3 groups (n=18. Then the porcelain surfaces were etched and bonded to composite with unfilled resin and finally observed under stereomicroscope. The data were analyzed with one-way ANOVA and Smirnov tests. Results: SEM analysis showed no difference between groups in terms of etch pattern. Microshear bond strength values for experimental, Kimia, and Ultradent HF were 28.53 (±4.92, 28.21 (±6.61, and 26.14 (±7.61 MPa, respectively. There was no significant difference between the bond strength of test groups (P0.05. Conclusion: Quality of experimental HF in terms of etch pattern, microshear bond strength and microleakage of composite/porcelain interface was similar to that of two commercial hydrofluoric acids.

  1. Synthesis of metallic glasses and metallic glass based composites in the Cu-Mo-Hf system by ion beam mixing

    Institute of Scientific and Technical Information of China (English)

    BAI Xue; WANG TongLe; CUI YuanYuan; DING Ning; LI JiaHao; LIU BaiXin


    Single-phase and dual-phase metallic glasses as well as metallic glass based composites were synthesized in the Cu-Mo-Hf ternary metal system by 200 keV xenon ion beam mixing of far-from-equilibrium.It was found that Mo-Hf-based and Cu-Mo-based single-phase metallic glasses could be obtained at compositions around Cu17Mo20Hf63 and Cu34Mo57Hf9,respectively.Interestingly,at the nearly equal-atomic stoichiometry of Cu38Mo31Hf31,a dual-phase Cu-Mo-Hf metallic glass,consisting both of the Mo-Hf-based and Cu-Mo-based phases,was first obtained at relatively low irradiation doses ranging from (1-5)×1015 Xe+/cm2,and a single-phase metallic glass was eventually obtained at a dose of 7×1015 Xe+/cm2.In addition,two glass-based composites were obtained at the compositions of Cu14Mo62Hf24 and Cu77Mo14Hf9,and they consisted of the Mo-Hf based and Cu-Mo based metallic glasses,dissolved with some uniformly distributed BCC Mo-based and FCC Cu-based crystalline solid solutions,respectively.The formation mechanism of the above described non-equilibrium alloy phases was also discussed in terms of the atomic collision theory.

  2. 湖南仙人岩与金矿床有关的二长岩锆石U-Pb年龄、Hf同位素及地质意义%Zircon U-Pb Geochronology and Hf Isotopic Compositions of the Monzonite,Related to the Xianrenyan Gold Deposit in Hunan Province and Its Geological Significances

    Institute of Scientific and Technical Information of China (English)

    甄世民; 祝新友; 李永胜; 杜泽忠; 公凡影; 巩小栋; 齐钒宇; 贾德龙; 王璐琳


    The Xianrenyan pluton is located in the south of Shuikoushan ore field, Hunan Province. There develops Au, Cu, Mo and Zn mineralization in inner and outer contact zones of the pluton, which shows the colse relationship between the pluton and the metallic mineralization. Zircon LA - MC - ICP -MS U - Pb age of the monzonite suggests a weighted mean age of (156. 09±0. 46) Ma (MSWD= 1. 4) which implies that the pluton was ernplaced in Early Yanshanian period. The in-situ Hf isotopic analysis reveals 176Hf/177Hf ratios in the zircon range from 0. 282 243 to 0. 282 904, and εHf(t) from —15. 55 to 7. 87 (with peak value around —10) , and the two stage Hf model ages(TDM2) from 703 Ma to 2 188 Ma (with peak value around 1 800 Ma), which indicates that parental magma of the pluton was derived from the mixed sources of the lower crust and mantle. Based on the geochemistry of the rocks, it can be concluded that the monzonite was mainly resulted from remelting of the Mesoproterozoic basement rocks and formed in Middle and Late Jurassic when the crust was in an extension-thinning geodynamic setting. In addition, the authors compare and analyze the lithogeochemical characteristics of the Xianrenyan pluton and the Shuikoushan stock. The fact that the Xianrenyan pluton has a weaker differentiation than the Shuikoushan pluton gives the reason for its unfavorable gold mineralization.%仙人岩岩体位于湖南水口山矿田的南部.岩体内外接触带上均见有不同程度的金、铜、钼、锌等矿化,反映出岩体与成矿存在着内在联系.二长岩中锆石的LA-MC-ICP-MS年代学研究表明,其U-Pb加权平均年龄值为(156.09±0.46)Ma(MSWD=1.4),显示为燕山早期侵位.锆石Lu-Hf同位素原位分析结果表明,176 Hf/177 Hf值为0.282 243~0.282 904,εHf (t)值为-15.55~7.87,峰值在-10左右,Hf同位素二阶段模式年龄(TDM2)为703~2 188 Ma,峰值在1 800 Ma左右,指示岩浆为壳幔混合来源.结合岩体的地球化学特征,认

  3. Age and genesis of the Myanmar jadeite: Constraints from U-Pb ages and Hf isotopes of zircon inclusions

    Institute of Scientific and Technical Information of China (English)

    QIU ZhiLi; WU FuYuan; YANG ShuFeng; ZHU Min; SUN JinFeng; YANG Ping


    Myanmar jadeite (jadeitite) is well known for its economical value and distinctive tectonic locality within the collisional belt between India and Eurasian plates. However, it is less studied for its genesis and geodynamic implications due to precipitous topography, adverse weather and local military conflicts in the area. By means of combined ICP-MS and LA-MC-ICPMS techniques, we have carried out in-situ trace elements, U-Pb and Lu-Hf isotopes for zircon inclusions in a piece of jadeite gem sample. CL imaging suggests that the zircons are metasomatic in origin, and contain mineral inclusions of jadeite and omphacite. Seventy-five analyses on 16 grains of the zircons yield a U-Pb age of 158±2 Ma. The Myanmar zircons differ from other types in that they have no significant Eu anomalies despite high HREE concentrations. Measured 176Hf/177Hf ratios range from 0.282976 to 0.283122, with an average value of 0.283066±7;εHf(t) value of 13.8±0.3 (n=75). These results indicate that the Myanmar jadeite was formed in the Late Jurassic, probably by interaction of fluid released from subducted oceanic slab with mantle wedge. Therefore, its formation has no genetic relationship to the continental collision between Indian and Euroasian plates.

  4. Petrogenesis of Jurassic fractionated I-type granites in Southeast China: Constraints from whole-rock geochemical and zircon U-Pb and Hf-O isotopes (United States)

    Zhang, Yang; Yang, Jin-Hui; Sun, Jin-Feng; Zhang, Ji-Heng; Chen, Jing-Yuan; Li, Xian-Hua


    Whole-rock geochemical and Sr-Nd-Hf isotopic data and zircon in situ U-Pb ages and Hf-O isotopes are reported for twelve granitic intrusions from inland to coastal areas of the Cathaysia Block, Southeast (SE) China, in order to constrain their magma sources and petrogenesis. They are mainly composed of biotite granites with minor granodiorites. Zircon U-Pb dating by LA-ICPMS and SIMS methods gave emplacement ages of 165-154 Ma for these rocks, which are metaluminous to weakly peraluminous (A/CNK = 0.95-1.10), with variable SiO2 contents and high K2O contents. They are all depleted in high field strength elements (HFSEs) and enriched in light rare earth elements (LREEs) and large ion lithophile elements (LILEs), and show negative Sr, Ba and Eu anomalies in the spidergrams. Petrographic and geochemical features suggest the granodiorites that contain hornblende to be typical of I-type, while the biotite granites without hornblende are fractionated I-type granites. Their variable major and trace element concentrations are due to fractional crystallization of feldspar, biotite, hornblende, and accessory minerals, including apatite, allanite and monazite. Moreover, our data indicate significant variations in isotopic compositions of these granitoids from inland to coastal areas. The inland granites, from the Lapu, Fogang, Xinfengjiang and Baishigang plutons, have relatively high initial 87Sr/86Sr ratios (0.7105-0.7155) and low εNd(t) (-11.2 to -7.3) and εHf(t) (-10.9 to -6.3) values for whole rocks, and variable δ18O values of 7.69-9.25‰ and εHf(t) values of -13.5 to -6.7 for zircons. In contrast, the coastal granites, from the Longwo, Wushikeng, Lianhuashan, Shigushan, Chiliao, Hulutian, Mantoushan and Fenghuang plutons, show relatively low initial 87Sr/86Sr ratios (0.7056-0.7110) and high εNd(t) (-7.6 to -6.2) and εHf(t) (-6.5 to -2.8) values for whole-rocks, together with εHf(t) values of -7.2 to 3.9 and δ18O values of 6.69-8.38‰ for zircons. The spatial

  5. The atomic structure and chemical composition of HfOx (x < 2) films prepared by ion-beam sputtering deposition (United States)

    Aliev, V. S.; Gerasimova, A. K.; Kruchinin, V. N.; Gritsenko, V. A.; Prosvirin, I. P.; Badmaeva, I. A.


    Non-stoichiometric HfOx films of different chemical composition (x partial pressure in a chamber. An effect of chemical composition on the atomic structure of the films was studied by reflection high-energy electron diffraction, x-ray photoelectron spectroscopy and field emission scanning electron microscopy methods. The films were found to be amorphous, consisting only of three components: Hf-metal clusters, Hf4O7 suboxide and stoichiometric HfO2. The relative concentration of these components varies with changing x. The surface of the films contains the increased oxygen content compared to the bulk. It was found that the Hf4O7 suboxide concentration is maximal at x = 1.8. The concept of hafnium oxide film growth by the IBSD method is proposed to explain the lack of suboxides variety in the films and the instability of HfO2, when annealed at high temperature.


    Energy Technology Data Exchange (ETDEWEB)

    Pizzarello, Sandra, E-mail: [Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85018-1604 (United States)


    HCN is ubiquitous in extraterrestrial environments and is central to current theories on the origin of early solar system organic compounds such as amino acids. These compounds, observed in carbonaceous meteorites, were likely important in the origin and/or evolution of early life. As part of our attempts to understand the origin(s) of meteoritic CN{sup –}, we have analyzed the {sup 15}N/{sup 14}N isotopic composition of HCN gas released from water extracts of the Murchison meteorite and found its value to be near those of the terrestrial atmosphere. The findings, when evaluated viz-a-viz molecular abundances and isotopic data of meteoritic organic compounds, suggest that HCN formation could have occurred during the protracted water alteration processes known to have affected the mineralogy of many asteroidal bodies during their solar residence. This was an active synthetic stage, which likely involved simple gasses, organic molecules, their presolar precursors, as well as mineral catalysts and would have lead to the formation of molecules of differing isotopic composition, including some with solar values.

  7. Multiple S isotopes, zircon Hf isotopes, whole-rock Sr-Nd isotopes, and spatial variations of PGE tenors in the Jinchuan Ni-Cu-PGE deposit, NW China (United States)

    Duan, Jun; Li, Chusi; Qian, Zhuangzhi; Jiao, Jiangang; Ripley, Edward M.; Feng, Yanqing


    Previous geochemical data for the Jinchuan Ni-Cu-(platinum-group elements, PGE) deposit, the single largest magmatic sulfide deposit in the world, are derived primarily from the upper parts of the deposit. This paper reports new PGE and S-Hf-Sr-Nd isotope data for the lower parts of the deposit that have become accessible for sampling by ongoing underground mining activity. New PGE data from this study, together with previous results, indicate that PGE tenors in the bulk sulfide ores of the deposit increase eastward, except for two fault-offset ore zones which occur together within the western part of the deposit. Generally, these two ore zones show depletions in IPGE (Ir, Ru, Rh) but not in PPGE (Pt, Pd) and Cu, and more fractionated olivine and Cr-spinel compositions than the rest of the deposit. These differences can be explained by a more evolved parental magma for the IPGE-depleted ore zones. The eastward increase of PGE tenors in the rest of the deposit can be explained by upgrading of preexisting sulfide liquid in a subhorizontal conduit by a new surge of magma moving through the conduit from west to east, which took place before the formation of the IPGE-depleted ore zones. The Jinchuan ultramafic rocks are characterized by elevated initial 87Sr/86Sr ratios from 0.7077 to 0.7093, negative ɛ Nd values from -9.2 to -10.5, and zircon ɛ Hf values from -4 to -7. These data indicate up to 20 % of crustal contamination in the Jinchuan magma. Four of nine multiple sulfur isotope analyses for the Jinchuan deposit show anomalous ∆33S values varying from 0.12 to 2.67 ‰. These results, together with elevated δ34S values (>2 ‰) for some of the samples analyzed previously by other researchers, indicate the involvement of external sulfur from Archean and Proterozoic sedimentary rocks. Modeling results based on our olivine data and magma compositions estimated previously by other researchers indicate that fractional crystallization did not play a major role in

  8. Reconciliation of the excess 176Hf conundrum in meteorites: Recent disturbances of the Lu-Hf and Sm-Nd isotope systematics (United States)

    Bast, Rebecca; Scherer, Erik E.; Sprung, Peter; Mezger, Klaus; Fischer-Gödde, Mario; Taetz, Stephan; Böhnke, Mischa; Schmid-Beurmann, Hinrich; Münker, Carsten; Kleine, Thorsten; Srinivasan, Gopalan


    The long-lived 176Lu-176Hf and 147Sm-143Nd radioisotope systems are commonly used chronometers, but when applied to meteorites, they can reveal disturbances. Specifically, Lu-Hf isochrons commonly yield dates up to ∼300 Myr older than the solar system and varying initial 176Hf/177Hf values. We investigated this problem by attempting to construct mineral and whole rock isochrons for eucrites and angrites. Meteorites from different parent bodies exhibit similar disturbance features suggesting that a common process is responsible. Minerals scatter away from isochron regressions for both meteorite classes, with low-Hf phases such as plagioclase and olivine typically being most displaced above (or left of) reference isochrons. Relatively Hf-rich pyroxene is less disturbed but still to the point of steepening Lu-Hf errorchrons. Using our Lu-Hf and Sm-Nd data, we tested various Hf and Lu redistribution scenarios and found that decoupling of Lu/Hf from 176Hf/177Hf must postdate the accumulation of significant radiogenic 176Hf. Therefore early irradiation or diffusion cannot explain the excess 176Hf. Instead, disturbed meteorite isochrons are more likely caused by terrestrial weathering, contamination, or common laboratory procedures. The partial dissolution of phosphate minerals may predominantly remove rare earth elements including Lu, leaving relatively immobile and radiogenic Hf behind. Robust Lu-Hf (and improved Sm-Nd) meteorite geochronology will require the development of chemical or physical methods for removing unsupported radiogenic Hf and silicate-hosted terrestrial contaminants without disturbing parent-daughter ratios.

  9. Geochronological, geochemical and Sr-Nd-Hf isotopic constraints on the petrogenesis of Late Cretaceous A-type granites from the Sibumasu Block, Southern Myanmar, SE Asia (United States)

    Jiang, Hai; Li, Wen-Qian; Jiang, Shao-Yong; Wang, He; Wei, Xiao-Peng


    The Late Cretaceous to Paleogene granitoids occur widespread in the Sibumasu block within Myanmar (SE Asia), which show a close association with tin-tungsten mineralization. However, the precise timing, petrogenesis and tectonic significance of these granitoids are poorly constrained so far. In this study, we present a detailed study on geochronology, elemental and Sr-Nd-Hf isotopic geochemistry for the Hermyingyi and Taungphila granites in southern Myanmar, with the aim of determining their petrogenesis and tectonic implications. LA-ICP-MS U-Pb dating of zircon grains from the two granites yield ages of 69-70 Ma, indicating a Late Cretaceous magmatic event. These granitic rocks are weakly peraluminous and belong to the high-K calc-alkaline series. They are both characterized by high SiO2, K2O + Na2O, FeOT/(FeOT + MgO) and Ga/Al ratios and low Al2O3, CaO, MgO, P2O5 and TiO2 contents, enriched in Rb, Th, U and Y, but depleted in Ba, Sr, P, and Eu, suggesting an A-type granite affinity. Moreover, they display prominent tetrad REE patterns and non-CHARAC trace element behavior, which are common in late magmatic differentiates with strong hydrothermal interaction or deuteric alteration. The granites belong to A2-type and probably formed at a high temperature and anhydrous condition. They have zircon εHf(t) values from - 12.4 to - 10.0 and whole-rock εNd(t) values from - 11.3 to - 10.6, with Paleoproterozoic TDM2 ages (1741-1922 Ma) for both Hf and Nd isotopes. Geochemical and isotopic data suggest that these A-type granites were derived from partial melting of the Paleoproterozoic continental crust dominated by metaigneous rocks with tonalitic to granodioritic compositions, without significant input of mantle-derived magma and followed by subsequent fractional crystallization. By integrating all available data for the regional tectonic evolution in SE Asia and adjacent regions, we attribute the formation of the Late Cretaceous A-type granites to a back-arc extension

  10. Hybrid genesis of Jurassic fayalite-bearing felsic subvolcanic rocks in South China: Inspired by petrography, geochronology, and Sr-Nd-O-Hf isotopes (United States)

    Guo, Chunli; Zeng, Lingsen; Li, Qiuli; Fu, Jianming; Ding, Tiping


    Fayalite-bearing felsic (FBF) magmatic rocks are a special type of granitic rocks with controversial origins. A suite of fayalite- and ferrosilite-bearing subvolcanic rocks, namely, the Xishan FBF rocks in South China, is investigated in this study. The Xishan FBF rocks have high SiO2 contents of 69-70 wt.%, high K2O/Na2O ratios of 1.71-1.95, and high FeOt/(FeOt + MgO) ratios of 0.88-0.89. Fayalite (Fo = 7.3-9.6) and ferrosilite (Fs = 74.1-76.5) minerals are found in the Xishan FBF rocks. According to the Unmix function of Isoplot, the zircon U-Pb ages and initial Hf isotope compositions are categorized into two groups with ages of 156.6 Ma and 151.5 Ma and εHf(t) values of - 7.1 and - 5.2, respectively. The minerals show δ18O values of 8.8-9.8‰ for zircon, 6.0-8.1‰ for fayalite, and 7.0-8.2‰ for ferrosilite. The oxygen isotope fractionations between ferrosilite and fayalite (ΔOpx-Ol) vary from - 0.8‰ to + 1.5‰, which indicates disequilibrium crystallization. Whole-rock analyses show high initial 87Sr/86Sr ratios of 0.7169 to 0.7180 and negative εNd(t) values of - 7.3 to - 6.8; zircon analyses show εHf(t) values of - 9.1 to - 3.8 and δ18O values of 8.8-9.8‰. So whole rock and zircon isotopes indicate a crustal signature. Based on these mineralogical and geochemical data, the Xishan FBF rocks were attributed to A-type granites and derived from the mixing of two batches of crustal magmas, which were all derived from the partial melting of ancient igneous protolith under the conditions of high temperature (683-893 °C), moderate water (3-5 wt.%), and low oxygen fugacity (lg fO2 = - 1.21). Such rigorous physical conditions may be common for the FBF igneous rocks all over the world, which may be the primary factors controlling occurrence of the FBF rocks in limited volume and quantity.

  11. Zircon U-Pb dating, geochemical and Sr-Nd-Hf isotopic characteristics of the Jintonghu monzonitic rocks in western Fujian Province, South China: Implication for Cretaceous crust-mantle interactions and lithospheric extension (United States)

    Li, Bin; Jiang, Shao-Yong; Lu, An-Huai; Zhao, Hai-Xiang; Yang, Tang-Li; Hou, Ming-Lan


    Comprehensive petrological, in situ zircon U-Pb dating, Ti-in-zircon temperature and Hf isotopic compositions, whole rock geochemical and Sr-Nd isotopic data are reported for the Jintonghu monzonitic intrusions in the western Fujian Province (Interior Cathaysia Block), South China. The Jintonghu monzonitic intrusions were intruded at 95-96 Ma. Their Sr-Nd-Hf isotopic compositions are similar to the coeval and nearby enriched lithospheric mantle-derived mafic and syenitic rocks, indicating that the Jintonghu monzonitic rocks were likely derived from partial melting of the enriched mantle sources. Their high Nb/Ta ratios (average 21.6) suggest that the metasomatically enriched mantle components were involved, which was attributed to the modification of slab-derived fluid and melt by the subduction of the paleo-Pacific Plate. The presence of mafic xenoliths, together with geochemical and isotopic features indicates a mafic-felsic magma mixing. Furthermore, the Jintonghu intrusions may have experienced orthopyroxene-, biotite- and plagioclase-dominated crystallization. Crust-mantle interaction can be identified as two stages, including that the Early Cretaceous mantle metasomatism and lithospheric extension resulted from the paleo-Pacific slab subduction coupled with slab rollback, and the Late Cretaceous crustal activation and enhanced extension induced by dip-angle subduction and the underplating of mantle-derived mafic magma.

  12. Petrogenesis of keratophyes in the Pingshui Group,Zhejiang: Constraints from zircon U-Pb ages and Hf isotopes

    Institute of Scientific and Technical Information of China (English)

    CHEN ZhiHong; XING GuangFu; GUO KungaYi; DONG YongGuan; CHEN Rong; ZENG Yong; LI LongMing; HE ZhengYu; ZHAO Ling


    Zircon LA-ICP-MS U-Pb ages and Hf isotopic as well as whole-rock geochemical data are reported for keratophyes in the Pingshui Group, Zhejiang. The results are used to discuss their petrogenesis and geological significance. The keratophyes were dated at 904±8 to 906±10 Ma. These intermediate-felsic rocks are characterized by high LREE contents end depletion of HREE and HFSE (e.g., Nb, Ta, Ti, P), resembling arc-derived rocks. The keratophyes exhibit positive εHf(t) values of 8.6 to 15.4, consistent with their εNd(t) values of 6.4 to 7.9 but far away from those of crust-derived rocks. Such features indicate that they were likely originated from prompt reworking of juvenile crust by arc-continent collision during the early-Neoproterozoic assembly between the Cathaysia and Yangtze Blocks. Combining with their Hf model ages, we suggest that there may exist not only remarkable growth of juvenile crust at ca.1.3-1.1 Ga but also production of juvenile arc-derived crust along the southeastern margin of the Yangtze Block (e.g., the Pingshui area) at ca.1.0-0.9 Ga.

  13. Timing and tectonic implications of the Pan-African Bangangte syenomonzonite, West Cameroon: Constraints from in-situ zircon U-Pb age and Hf-O isotopes (United States)

    Tchouankoue, Jean Pierre; Li, Xian-Hua; Belnoun, Rose Noel Ngo; Mouafo, Lucas; Ferreira, Valderez Pinto


    The Bangangte pluton is a SW-NE elongated (5 × 20 km) massif located in the southeastern part of the Pan-African North Equatorial Fold Belt in Cameroon, consisting of two units with dominant monzonites in the south and syenites in the north. SIMS U-Pb zircon dating yields consistent emplacement ages of 585 ± 4 Ma and 583 ± 4 Ma for the southern unit and the northern unit, respectively. The Bangangte rocks display typical shoshonitic compositions characterized by Na2O + K2O > 5 wt%, K2O/Na2O ∼2, enrichment in LILE and LREE, but depletion in HFSE. Rocks from both units have similar O-Hf isotopes, with the monzonite zircons from the southern unit showing slightly higher δ18O (7.0 ± 0.4‰) but lower εHf(t) (-15.3 ± 1.4) value than the syenite zircons from southern unit (δ18O = 6.0 ± 0.4‰; εHf(t) = -14.0 ± 2.0). They were generated by partial melting of an enriched mantle source metasomatized by previous subduction processes, accompanied by crystal fractionation of pyroxene, Ti-Fe oxides and apatite, as well as crustal contamination to varying degrees. These rocks display a transitional geochemical feature of the subduction-related and within-plate shoshonites, suggesting that they were most likely emplaced in a post-collisional setting at the waning stage of the Pan-African orogeny.

  14. Neoarchean (2.5–2.8 Ga crustal growth of the North China Craton revealed by zircon Hf isotope: A synthesis

    Directory of Open Access Journals (Sweden)

    Andong Wang


    Full Text Available The crustal growth of the North China Craton (NCC during the Neoarchean time (2.5–2.8 Ga is a hotly controversial topic, with some proposing that the main crustal growth occurred in the late Neoarchean (2.5–2.6 Ga, in agreement with the time of the magmatism, whereas others suggest that the main crustal accretion took place during early Neoarchean time (2.7–2.8 Ga, consistent with the time of crustal-formation of other cratons in the world. Zircon U-Pb ages and Hf isotope compositions can provide rigorous constraints on the time of crustal growth and the evolution and tectonic division of the NCC. In this contribution, we make a comprehensive review of zircon Hf isotope data in combination with zircon U-Pb geochronology and some geochemistry data from various divisions of the NCC with an aim to constrain the Neoarchean crustal growth of the NCC. The results suggest that both 2.7–2.8 Ga and 2.5–2.6 Ga crustal growth are distributed over the NCC and the former is much wider than previously suggested. The Eastern block is characterized by the main 2.7–2.8 Ga crustal growth with local new crustal-formation at 2.5–2.6 Ga, and the Yinshan block is characterized by ∼2.7 Ga crustal accretion as revealed by Hf-isotope data of detrital zircons from the Zhaertai Group. Detrital zircon data of the Khondalite Belt indicate that the main crustal growth period of the Western block is Paleoproterozoic involving some ∼2.6 Ga and minor Early- to Middle-Archean crustal components, and the crustal accretion in the Trans-North China Orogen (TNCO has a wide age range from 2.5 Ga to 2.9 Ga with a notable regional discrepancy. Zircon Hf isotope compositions, coupled with zircon ages and other geochemical data suggest that the southern margin may not be an extension of the TNCO, and the evolution and tectonic division of the NCC is more complex than previously proposed, probably involving multi-stage crustal growth and subduction processes

  15. The isotopic composition of CO in vehicle exhaust (United States)

    Naus, Stijn; Röckmann, Thomas; Popa, Elena


    The isotopic composition of atmospheric carbon monoxide (CO) and its sources can be a powerful tool to help constrain the CO budget, but data on the isotopic composition of CO sources is sparse. We investigated the isotopic composition (13C16O and 12C18O) of one of the main sources of CO in urban areas: traffic emissions. Samples from individual passenger cars and atmospheric samples from polluted areas were measured. The results show strong indications that CO emissions from traffic are dominated by a small subset of cars or driving conditions, which, in this study, were cold petrol cars. The spread in isotopic composition of the full dataset was large, but this dominant subset showed a relatively stable isotopic composition. Therefore, the individual car samples result in a well-defined overall traffic signature, which was in agreement with the atmospheric isotopic signature derived from the atmospheric samples.

  16. Evaluating the provenance of Permian-Triassic and Palaeocene-Eocene ash beds by high precision U-Pb and Lu-Hf isotopic analyses of zircons: linking local sedimentary records to global events (United States)

    Eivind Augland, Lars; Jones, Morgan; Planke, Sverre; Svensen, Henrik; Tegner, Christian


    Zircons are a powerful tool in geochronology and isotope geochemistry, as their affinity for U and Hf in the crystal structure and the low initial Pb and Lu allow for precise and accurate dating by U-Pb ID-TIMS and precise and accurate determination of initial Hf isotopic composition by solution MC-ICP-MS analysis. The U-Pb analyses provide accurate chronostratigraphic controls on the sedimentary successions and absolute age frames for the biotic evolution across geological boundaries. Moreover, the analyses of Lu-Hf by solution MC-ICP-MS after Hf-purification column chemistry provide a powerful and robust fingerprinting tool to test the provenance of individual ash beds. Here we focus on ash beds from Permian-Triassic and Palaeocene successions in Svalbard and from the Palaeocene-Eocene Thermal Maximum (PETM) in Fur, Denmark. Used in combination with whole rock geochemistry from the ash layers and the available geochemical and isotopic data from potential source volcanoes, these data are used to evaluate the provenance of the Permian-Triassic and Palaeocene ashes preserved in Svalbard and PETM ashes in Denmark. If explosive eruptions from volcanic centres such as the Siberian Traps and the North Atlantic Igneous Province (NAIP) can be traced to distal basins as ash layers, they provide robust tests of hypotheses of global synchronicity of environmental changes and biotic crises. In addition, the potential correlation of ash layers with source volcanoes will aid in constraining the extent of explosive volcanism in the respective volcanic centres. The new integrated data sets will also contribute to establish new reference sections for the study of these boundary events when combined with stable isotope data and biostratigraphy.

  17. Hf-Nd Isotopes in West Philippine Basin Basalts: Results from International Ocean Discovery Program (IODP) Site U1438 and Implications for the Early History of the Izu-Bonin-Mariana (IBM) Subduction System (United States)

    Yogodzinski, G. M.; Hocking, B.; Bizimis, M.; Hickey-Vargas, R.; Ishizuka, O.; Bogus, K.; Arculus, R. J.


    Drilling at IODP Site U1438, located immediately west of Kyushu-Palau Ridge (KPR), the site of IBM subduction initiation, penetrated 1460 m of volcaniclastic sedimentary rock and 150 m of underlying basement. Biostratigraphic controls indicate a probable age for the oldest sedimentary rocks at around 55 Ma (51-64 Ma - Arculus et al., Nat Geosci in-press). This is close to the 48-52 Ma time period of IBM subduction initiation, based on studies in the forearc. There, the first products of volcanism are tholeiitic basalts termed FAB (forearc basalt), which are more depleted than average MORB and show subtle indicators of subduction geochemical enrichment (Reagan et al., 2010 - Geochem Geophy Geosy). Shipboard data indicate that Site U1438 basement basalts share many characteristics with FABs, including primitive major elements (high MgO/FeO*) and strongly depleted incompatible element patterns (Ti, Zr, Ti/V and Zr/Y below those of average MORB). Initial results thus indicate that FAB geochemistry may have been produced not only in the forearc, but also in backarc locations (west of the KPR) at the time of subduction initiation. Hf-Nd isotopes for Site 1438 basement basalts show a significant range of compositions from ɛNd of 7.0 to 9.5 and ɛHf of 14.5 to 19.8 (present-day values). The data define a well-correlated and steep array in Hf-Nd isotope space. Relatively radiogenic Hf compared to Nd indicates an Indian Ocean-type MORB source, but the dominant signature, with ɛHf >16.5, is more radiogenic than most Indian MORB. The pattern through time is from more-to-less radiogenic and more variable Hf-Nd isotopes within the basement section. This pattern culminates in basaltic andesite sills, which intrude the lower parts of the sedimentary section. The sills have the least radiogenic compositions measured so far (ɛNd ~6.6, ɛHf ~13.8), and are similar to those of boninites of the IBM forearc and modern IBM arc and reararc rocks. The pattern within the basement

  18. Magnetic dipole moments of High-K isomeric states in Hf isotopes

    CERN Multimedia

    Walters, W; Nishimura, K; Bingham, C R


    It is proposed to make precision measurements of the magnetic moments of 5 multi-quasi-particle K-isomers in Hf nuclei by the Nuclear Magnetic Resonance of Oriented Nuclei (NMR/ON) technique using the NICOLE on-line nuclear orientation facility and exploiting the unique HfF$_{3}$ beams recently available at ISOLDE. Results will be used to extract single-particle and collective g-factors of the isomeric states and their excitations and to shed new light on their structure.

  19. Situation of sewage input reflected by nitrogen isotopic composition in a sediment core of Hongfeng Lake

    Institute of Scientific and Technical Information of China (English)


    Nitrogen in Hongfeng South Lake water mainly comes from sewage with high N concentrations from Pingba Chemical Fertilizer Plant (PCFP). Studies on the sediment core HF010427 sampled in the lake showed that the upward increase of nitrogen isotopic composition of sedimentary organic nitrogen (δ15Norg) accorded with the trend of industrial total production (TP) of PCFC. On the contrary, diagenesis will theoretically cause an upward decrease of δ15Norg. Because no treatment of sewage water was carried out, TP corresponds with sewage emission, indicating that sedimentary δ15Norg can reflect well the total trend of sewage input. The very similar profile shape between nitrogen isotopic composition of sedimentary absorbed ammonium (δ15NH4+absorbed) and TP of PCFP suggests that δ15NH4+absorbed can be used to reconstruct more detailed situation of sewage input. The study has a reference to history investigation of sewage input.

  20. Effect of three porcelain etchants type (HF-APF-PHA on porcelain- composite shear bond strength

    Directory of Open Access Journals (Sweden)

    Kermanshah H.


    Full Text Available Statement of Problem: Porcelain restorations are susceptible to fracture and a common method for repairing is the use of silane and composite on etched porcelain. Although HF is very effective in porcelain etching but has detrimental effects on tissues. Purpose: In this study, the effect of APF and PHA was compared with HF in porcelain etching. Also the role of silane, unfilled resin and dentin bonding in bond strength of composite- porcelain was evaluated. Methods and Materials: In this experimental in-vitro study, one-hundred twenty porcelain square blocks (552 mm were prepared and bonding surfaces of each sandblasted. Samples were divided into three groups. The first group (n=40 were etched with buffered HF 9.5% (Ultradent for 1 min., the second group (n=40 were etched with Iranian APF 1.23% (Kimia for 10 minutes and the third group (n=40 were etched with Iranian PHA 37% (Kimia for 1 min. Ultradent silane was applied on the surfaces of half of cases in each group. On the surfaces of half of silane-treated samples unfilled resin was applied and dentin bonding was used on the surfaces of the remaining. Samples without silane were treated in a similar manner. Composite cylinder with 4mm diameter and 2 mm height was bonded to porcelain. Specimens were stored in 37°C distilled water for 24 hours and subjected to 500 cycles. Shear bond strength was measured with an Instron machine and type of fracture was evaluated using a stereomicroscope. Results were analyzed using 3 way ANOVA, Kaplan- Maier and Tukey HSD tests. Results: Findings showed that PHA and APF roughened the porcelain surface without creating retentive micro undercuts but HF etches porcelain and creates retentive microundercuts. Ultradent silane had no significant effect on bond strength of porcelain- composite. Unfilled resin with Ultradent silane compared with dentin bonding with the same silane is more effective in bond strength of composite- porcelain. Conclusion: Based on

  1. Exotic crustal components at the northern margin of the Bohemian Massif-Implications from Usbnd Thsbnd Pb and Hf isotopes of zircon from the Saxonian Granulite Massif (United States)

    Sagawe, Anja; Gärtner, Andreas; Linnemann, Ulf; Hofmann, Mandy; Gerdes, Axel


    The Saxonian Granulite Massif is located at the northern margin of the Saxo-Thuringian Zone of the peri-Gondwana Bohemian Massif. Eight felsic and mafic granulites were studied with respect to their geochemistry and Usbnd Pb zircon geochronology. The felsic granulites are interpreted to be derived from continental crust of possible granitoid composition. An origin from depleted mantle sources with IAT to MORB composition can be assumed for the mafic granulites. The peak of metamorphism is thought to be timed at about 340 Ma, while several earlier metamorphic events are supposed to have occurred at about 355-360, 370-375, 405, and 450 Ma. They reveal a complex and polyphased geologic evolution of the Saxonian Granulite Massif. Protolith emplacement likely took place at c. 450 and 494 Ma. Hf isotopic data suggest Mesoproterozoic crustal ages at least for parts of the massif. As these crustal ages are exotic for the Bohemian Massif, their origin has to be searched elsewhere. Potential source areas could be Amazonia and Baltica, of which the latter is the one preferred. Furthermore, a composite architecture with at least two components-the felsic granulites with Mesoproterozoic crustal model ages, and the mafic granulites of potential island arc origin-is hypothesised. Their amalgamation to the recent appearance of the Saxonian Granulite Massif is likely bracketed between 375 and 340 Ma.

  2. Lu2O3:Pr,Hf Storage Phosphor: Compositional and Technological Issues

    Directory of Open Access Journals (Sweden)

    Aneta Wiatrowska


    Full Text Available Lu2O3:Pr,Hf ceramics were investigated using mainly thermoluminescence (TL technique. Their ability to efficiently store energy acquired upon irradiation with X-rays was proven. The best TL performance was achieved for compositions containing 0.025%–0.05% of Pr and about 0.1% of Hf. Further enhancement of TL efficiency was attained by increasing the temperature of sintering of the ceramics up to 1700 °C and applying reducing atmosphere of forming gas. It was also proven that fast cooling after the sintering at 1700 °C significantly enhanced the storage phosphor performance. TL glow curve contained three components peaking around 130, 250 and 350 °C. Among them, the one at 250 °C contributed the most to the total TL.

  3. Three-Dimensional FIB/EBSD Characterization of Irradiated HfAl3-Al Composite

    Energy Technology Data Exchange (ETDEWEB)

    Hua, Zilong; Guillen, Donna Post; Harris, William; Ban, Heng


    A thermal neutron absorbing material, comprised of 28.4 vol% HfAl3 in an Al matrix, was developed to serve as a conductively cooled thermal neutron filter to enable fast flux materials and fuels testing in a pressurized water reactor. In order to observe the microstructural change of the HfAl3-Al composite due to neutron irradiation, an EBSD-FIB characterization approach is developed and presented in this paper. Using the focused ion beam (FIB), the sample was fabricated to 25µm × 25µm × 20 µm and mounted on the grid. A series of operations were carried out repetitively on the sample top surface to prepare it for scanning electron microscopy (SEM). First, a ~100-nm layer was removed by high voltage FIB milling. Then, several cleaning passes were performed on the newly exposed surface using low voltage FIB milling to improve the SEM image quality. Last, the surface was scanned by Electron Backscattering Diffraction (EBSD) to obtain the two-dimensional image. After 50 to 100 two-dimensional images were collected, the images were stacked to reconstruct a three-dimensional model using DREAM.3D software. Two such reconstructed three-dimensional models were obtained from samples of the original and post-irradiation HfAl3-Al composite respectively, from which the most significant microstructural change caused by neutron irradiation apparently is the size reduction of both HfAl3 and Al grains. The possible reason is the thermal expansion and related thermal strain from the thermal neutron absorption. This technique can be applied to three-dimensional microstructure characterization of irradiated materials.

  4. Magnesium Isotopic Composition of Subducting Marine Sediments (United States)

    Hu, Y.; Teng, F. Z.; Plank, T. A.; Huang, K. J.


    Subducted marine sediments have recently been called upon to explain the heterogeneous Mg isotopic composition (δ26Mg, ‰) found in mantle wehrlites (-0.39 to +0.09 [1]) in the context of a homogeneous mantle (-0.25 ± 0.07 [2]). However, no systematic measurements of δ26Mg on marine sediments are currently available to provide direct support to this model. To characterize the Mg inputs to global subduction zones, we measured δ26Mg data for a total of 90 marine sediments collected from 12 drill sites outboard of the world's major subduction zones. These sediments span a 1.73‰ range in δ26Mg. The detritus-dominated sediments have δ26Mg (-0.59 to +0.53) comparable to those of weathered materials on continents (e.g. -0.52 to +0.92 [3]), while the calcareous oozes yield δ26Mg (as light as -1.20) more similar to the seawater value (-0.83 [4]). The negative correlation between δ26Mg and CaO/Al2O3 in these sediments indicates the primary control of mineralogy over the Mg isotopic distribution among different sediment types, as carbonates are enriched in light Mg isotopes (-5.10 to -0.40 [5]) whereas clay-rich weathering residues generally have heavier δ26Mg (e.g. up to +0.65 in saprolite [6]). In addition, chemical weathering and grain-size sorting drive sediments to a heavier δ26Mg, as indicated by the broad positive trends between δ26Mg with CIA (Chemical Index of Alteration [7]) and Al2O3/SiO2, respectively. Collectively, the arc systems sampled in this study represent ~30% of global arc length and the extrapolated global Mg flux of subducting marine sediments accounts for ~9% of the yearly Mg riverine input with a flux-weighted average δ26Mg at -0.26. Subduction of these heterogeneous sediments may not cause significant mantle heterogeneity on a global scale, but the highly variable Mg fluxes and δ26Mg of sediments delivered to different trenches are capable of producing local mantle variations. Volcanic rocks sourced from these mantle domains are thus

  5. Implications for the evolution of continental crust from Hf isotope systematics of Archean detrital zircons (United States)

    Stevenson, Ross K.; Patchett, P. Jonathan


    Results from the fractionation of zircon by sedimentary processes into continental margin sandstone yield information on the preservation of preexisting continental crust in the form of zircon, making it possible to distinguish between the contrasting theories of gradual growth versus constant volume of continental crust over geologic time. In this work, Hf-176/Hf-177 ratios were determined for detrital zircon fractions from 2.0-2.5, 2.6-3.0, and pre-3.0 Gyr old sandstones from the Canadian-Shield, the North-Atlantic, the Wyoming, and the Kaapvaal Cratons. Results pointed to small amounts of continental crust prior to 3.0 Gyr ago and a rapid addition of continental crust between 2.5 and 3.0 Gyr ago, consistent with the gradual growth of continental crust, and giving evidence against no-growth histories.

  6. Angular momentum limit of Hf isotopes produced in three fusion-evaporation reactions

    CERN Document Server

    Domscheit, J; Ernst, J; Fallon, P; Herskind, B; Hübel, H; Korten, W; Lee, I Y; Macchiavelli, A O; Nenoff, N; Siem, S; Ward, D; Wilson, J N


    The compound nucleus sup 1 sup 6 sup 8 Hf was populated in three fusion-evaporation reactions with different beam-target mass asymmetries: sup 5 sup 0 Ti+ sup 1 sup 1 sup 8 Sn, sup 6 sup 4 Ni+ sup 1 sup 0 sup 4 Ru and sup 7 sup 4 Ge+ sup 9 sup 4 Zr. Due to the large negative Q values of these reactions the compound nucleus is formed at low excitation energy. At three or four excitation energies for each reaction gamma-ray spectra of the evaporation residues sup 1 sup 6 sup 6 Hf to sup 1 sup 6 sup 3 Hf, corresponding to the 2n to 5n exit channels, respectively, were recorded with the Ge detectors of the 8 pi-spectrometer array. The gamma-ray multiplicity and total energy were measured using the inner ball of BGO detectors. This data was used to determine the maximum angular momentum transferred to each evaporation channel, the gamma-ray decay entry region and the relative cross sections. No differences are observed between the three reactions. This is explained by the very similar dependence of the excitation ...

  7. Comprehensive analysis for major, minor and trace element contents and Sr-Nd-Pb-Hf isotope ratios in sediment reference materials, JSd-1 and MAG-1

    Digital Repository Service at National Institute of Oceanography (India)

    Nath, B.N.; Makishima, A.; Noordmann, J.; Tanaka, R.; Nakamura, E.

    In view of the requirement of a well-characterized and easily available aquatic sediment reference material, a comprehensive analysis comprising of fifty major, minor and trace elements as well as Sr–Nd–Pb–Hf isotopes were carried out...

  8. Phase composition of Bi2O3 specimens doped with Ti, Zr and Hf

    Directory of Open Access Journals (Sweden)

    Poleti Dejan


    Full Text Available Powder mixtures of α-Bi2O3 containing 2, 5 and 10 mole % of TiO2, ZrO2 or HfO2 were homogenized, heated at 820ºC for 24 h and quenched in air. X-ray powder diffraction technique was used to characterize the prepared samples. In all cases metastable Bi2O3 polymorphs, γ-Bi2O3 or β-Bi2O3, are found as single or major phases. Addition of Ti4+ ions stabilizes γ-Bi2O3 polymorph, while either Zr4+ or Hf4+ ions stabilize β-Bi2O3 polymorph. In the samples with 2 and 5 mole % of TiO2 the presence of even two γ-Bi2O3 phases (Bi12TiO20 compound and a very low Ti-doped γ-Bi2O3 was established. Similarly, in the sample with 2 mole % of HfO2 two β-Bi2O3 phases were found. Phase composition of prepared samples, values of unit cell parameters and the appearance of two polymorphs with identical crystal structure but different unit cell parameters are discussed and compared with known data.

  9. Juvenile crust formation in the Zimbabwe Craton deduced from the O-Hf isotopic record of 3.8-3.1 Ga detrital zircons (United States)

    Bolhar, Robert; Hofmann, Axel; Kemp, Anthony I. S.; Whitehouse, Martin J.; Wind, Sandra; Kamber, Balz S.


    Hafnium and oxygen isotopic compositions measured in-situ on U-Pb dated zircon from Archaean sedimentary successions belonging to the 2.9-2.8 Ga Belingwean/Bulawayan groups and previously undated Sebakwian Group are used to characterize the crustal evolution of the Zimbabwe Craton prior to 3.0 Ga. Microstructural and compositional criteria were used to minimize effects arising from Pb loss due to metamorphic overprinting and interaction with low-temperature fluids. 207Pb/206Pb age spectra (concordance >90%) reveal prominent peaks at 3.8, 3.6, 3.5, and 3.35 Ga, corresponding to documented geological events, both globally and within the Zimbabwe Craton. Zircon δ18O values from +4 to +10‰ point to both derivation from magmas in equilibrium with mantle oxygen and the incorporation of material that had previously interacted with water in near-surface environments. In εHf-time space, 3.8-3.6 Ga grains define an array consistent with reworking of a mafic reservoir (176Lu/177Hf ∼0.015) that separated from chondritic mantle at ∼3.9 Ga. Crustal domains formed after 3.6 Ga depict a more complex evolution, involving contribution from chondritic mantle sources and, to a lesser extent, reworking of pre-existing crust. Protracted remelting was not accompanied by significant mantle depletion prior to 3.35 Ga. This implies that early crust production in the Zimbabwe Craton did not cause complementary enriched and depleted reservoirs that were tapped by later magmas, possibly because the volume of crust extracted and stabilised was too small to influence (asthenospheric) mantle isotopic evolution. Growth of continental crust through pulsed emplacement of juvenile (chondritic mantle-derived) melts, into and onto the existing cratonic nucleus, however, involved formation of complementary depleted subcontinental lithospheric mantle since the early Archaean, indicative of strongly coupled evolutionary histories of both reservoirs, with limited evidence for recycling and lateral

  10. Isotopic compositional Characteristics of Terrigenous Natural Gases in China

    Institute of Scientific and Technical Information of China (English)

    沈平; 徐永昌


    The C and H isotopic compositions of the methane in more than 160 gas samples from 10 basins in China are presented in this paper.The natural gases are classified as four types: biogenic gas ,bio-thermocatalytic transitional gas, gas associated with condensate oil ,and coal-type gas. The isotopic compositions of these gases closely related to the depositional basins, the types of organic matter,the stages of thermal evolution and the genetic characteristics of different gas reservoirs.Studies of the C and H isotopic compositions of terrigenous natural gases will provide valua-ble information on the prospecting and development of natural gases of different genetic types.

  11. U-Pb Ages and Hf Isotope Compositions of Detrital Zircons from the Sandstone in the Early Cretaceous Wawukuang Formation in the Jiaolai Basin, Shandong Province and its Tectonic Implications%胶莱盆地早白垩世瓦屋夼组砂岩中碎屑锆石U-Pb-Hf同位素组成及其构造意义

    Institute of Scientific and Technical Information of China (English)

    霍腾飞; 杨德彬; 许文良; 王枫; 刘海彬; 师江朋


    LA-ICP-MS U-Pb dating and in situ Hf isotope analysis were carried out for the detrital zircons to constrain the depositional age and provenance of the Wawukuang Formation, which is believed as the earliest unit of the Laiyang Group in the Jiaolai Basin, and its implications. Most of these detrital zircons from the feldspar quartz sandstone in the Wawukuang Formation are magmatic in origin, which are euhedral-subhedral and display oscillatory zoning in CL images; whereas few Late Triassic detrital zircons are metamorphic in origin and structureless in CL images. U-Pb isotopic dating of 82 zircon grains yields age populations at ca. 129 Ma, 158 Ma, 224 Ma, 253 Ma, 461 Ma, 724 Ma, 1851 Ma and 2456 Ma. U-Pb dating and Hf isotopic results indicate that:1) the Wawukuang Formation deposited during the Early Cretaceous (129–106 Ma);2) the detrital zircons with the ages of 1851 Ma and 2456 Ma mainly sourced from the Precambrian basement rocks of the North China Craton;the Neoproterozoic (729–721 Ma) magmatic zircons and the Late Triassic (226–216 Ma) metamorphic zircons sourced from the Su-Lu terrane; The Late Paleozoic detrital zircons could source from the Late Paleozoic igneous rocks in the northern margin of the North China Craton;the Late Triassic (231–223 Ma) magmatic zircons and the 158–129 Ma zircons sourced from the coeval igneous rocks in the Jiaobei and Jiaodong;3) the deposition age and provenance of the Jiaolai Basin are different from those of the Hefei Basin; 4) the recognition of clastic sediments from the Su-Lu terrane in the Wawukuang Formation suggests that the Su-Lu terrane was under denudation in the Early Cretaceous.%本文报道了胶莱盆地莱阳群最底部瓦屋夼组长石石英砂岩中碎屑锆石的LA-ICP-MS U-Pb年代学和原位Hf同位素分析结果,进而约束了瓦屋夼组砂岩的沉积时代和物源及其构造意义。碎屑锆石多数呈自形–半自形晶,发育岩浆生长环带,暗示它们为岩浆成因

  12. Isotope composition and volume of Earth’s early oceans


    Pope, Emily C.; Bird, Dennis K.; Rosing, Minik T.


    Oxygen and hydrogen isotope compositions of Earth’s seawater are controlled by volatile fluxes among mantle, lithospheric (oceanic and continental crust), and atmospheric reservoirs. Throughout geologic time the oxygen mass budget was likely conserved within these Earth system reservoirs, but hydrogen’s was not, as it can escape to space. Isotopic properties of serpentine from the approximately 3.8 Ga Isua Supracrustal Belt in West Greenland are used to characterize hydrogen and oxygen isotop...

  13. The Late Quaternary Oxygen Isotope Composition of Lake Michigan (United States)

    MacDonald, R. A.; Longstaffe, F. J.; Crowe, A. S.


    We present stable isotope records for porewater (oxygen, hydrogen) and biogenic carbonates (oxygen, carbon; ostracode and clam shells) in sediment cores from the Chippewa, Milwaukee and South Chippewa Basins of Lake Michigan. The oxygen and hydrogen isotope compositions of porewater from the South Chippewa Basin core showed very little variation with depth. At the maximum depth of 16.6m, δ18O values were within 2‰ and δD values were within 12‰ of modern Lake Michigan water (average δ18O = -5.9‰; average δD = -45‰); original porewater compositions have not been preserved. The oxygen isotope results for the biogenic carbonates, by comparison, provide a record of the isotopic composition of Lake Michigan over the last ~11,000 years, including significant incursions of very low-18O water, as first reported by Colman et al. (1990) and Forester et al. (1994). The low-18O waters originated from the retreating Laurentide ice sheet and may have been routed through Lakes Agassiz and Superior and discharged as large volumes over very short intervals of time. Periods characterized by much higher oxygen isotope compositions likely record the isotopic composition of regional precipitation over the catchment area. In summary, the large variations in the oxygen isotope composition of early Lake Michigan water arose from regional climate change and changing water sources during the times of ice-sheet retreat.

  14. Tracing source terranes using U-Pb-Hf isotopic analysis of detrital zircons: provenance of the Orhanlar Unit of the Palaeotethyan Karakaya subduction-accretion complex, NW Turkey (United States)

    Ustaömer, Timur; Ayda Ustaömer, Petek; Robertson, Alastair; Gerdes, Axel


    Sandstones of the Late Palaeozoic-Early Mesozoic Karakaya Complex are interpreted to have accumulated along an active continental margin related to northward subduction of Palaeotethys. The age of deposition and provenance of the sandstones are currently being determined using radiometric dating of detrital zircons, coupled with dating of potential source terranes. Our previous work shows that the U-Pb-Hf isotopic characteristics of the sandstones of all but one of the main tectonostratigraphic units of the Karakaya Complex are compatible with a provenance that was dominated by Triassic and Permo-Carboniferous magmatic arc-type rocks, together with a minor contribution from Lower to Mid-Devonian igneous rocks (Ustaömer et al. 2015). However, one of the tectono-stratigraphic units, the Orhanlar Unit, which occurs in a structurally high position, differs in sedimentary facies and composition from the other units of the Karakaya Complex. Here, we report new isotopic age data for the sandstones of the Orhanlar Unit and also from an extensive, associated tectonic slice of continental metamorphic rocks (part of the regional Sakarya Terrane). Our main aim is to assess the provenance of the Orhanlar Unit sandstones in relation to the tectonic development of the Karakaya Complex as a whole. The Orhanlar Unit is composed of shales, sandstone turbidites and debris-flow deposits, which include blocks of Devonian radiolarian chert and Carboniferous and Permian neritic limestones. The sandstones are dominated by rock fragments, principally volcanic and plutonic rocks of basic-to-intermediate composition, metamorphic rocks and chert, together with common quartz, feldspar and mica. This modal composition contrasts significantly with the dominantly arkosic composition of the other Karakaya Complex sandstones. The detrital zircons were dated by the U-Pb method, coupled with determination of Lu-Hf isotopic compositions using a laser ablation microprobe attached to a multicollector

  15. Isotopic composition of precipitation in Ljubljana (Slovenia

    Directory of Open Access Journals (Sweden)

    Polona Vreča


    Full Text Available The stable isotopic composition of hydrogen and oxygen (δ2H and δ18O and tritium activity (3H are monitored in monthly precipitation at Ljubljana since 1981. Here we present complete set of numerical data and the statistical analysis for period 1981–2006. Seasonal variations of δ2H and δ18O are observed and are typical for continental stations of the Northern Hemisphere. The weighted mean δ2H and δ18O values are –59 ‰ and –8.6 ‰, respectively.The orthogonal Local Meteoric Water Line is δ2H = (8.06 ± 0.08δ18O + (9.84 ± 0.71, and the temperature coefficient of δ18O is 0.29 ‰/°C. Deuterium excess weighted mean value is 9.5 ‰ and indicates the prevailing influence of the Atlantic air masses. Tritium activity in monthly precipitation shows also seasonal variations which are superposed to the decreasing trend of mean annual activity.

  16. HFSE (High Field Strength Elements)-transport and U-Pb-Hf isotope homogenization mediated by Ca-bearing aqueous fluids at 2.04 Ga: Constraints from zircon, monazite, and garnet of the Venetia Klippe, Limpopo Belt, South Africa (United States)

    Zeh, A.; Gerdes, A.


    Results from laser-ablation inductively-coupled-plasma mass spectrometry (LA-ICP-MS) and isotope dilution (ID) analyses of minerals and rocks from a single outcrop of the Venetia Klippe of the Limpopo Belt indicate that the U-Pb and Hf isotope system homogenized on the decimetre scale under amphibolite-facies conditions of ⩽645 ± 25 °C and ⩽7.0 ± 1.1 kbar, i.e. in the presence of an aqueous fluid phase. For a metabasite sample, homogenization is supported by isotope analyses of metamorphic zircon, garnet, and whole rock, which yield a six-point Lu-Hf isochron age of 2039.7 ± 3.4 Ma, with initial 176Hf/177Hf of 0.28126 ± 0.00001, and a U-Pb zircon age of 2042 ± 10 Ma. The occurrence of a few inherited magmatic zircon cores with ages up to 2705 Ma, and with significantly lower initial 176Hf/177Hf of 0.28112, however, indicate that homogenization was incomplete. For a chlorite-biotite-garnet schist isotope homogenization is reflected by within error identical zircon and monazite U-Pb ages of 2045 ± 10 Ma and 2041 ± 8 Ma, respectively, and by a zircon-garnet-whole rock Lu-Hf isochron age of 2083 ± 63 Ma, with an initial 176Hf/177Hf of 0.28140 ± 0.00003. Contemporaneous formation of metamorphic zircon, monazite and garnet in the chlorite schist is not only supported by the isotope data, but also by chlorite inclusions in all three minerals, and by inclusions of metamorphic zircon in garnet. The inclusion textures and the identical initial 176Hf/177Hf support the conclusion that metamorphic zircon grains precipitated from an aqueous fluid phase, after dissolution of zirconium-bearing phases elsewhere, followed by a major HFSE transport, and Hf isotope homogenization. This fluid perhaps was Ca-bearing, as is suggested by the fact that garnet in the schist sample is the only Ca-bearing phase, and that metamorphic monazite, dating the metamorphic peak, is partially replacement by apatite. The fact that the metamorphic zircon rims in the metabasite sample have

  17. Paleoproterozoic tectonic transition from collision to extension in the eastern Cathaysia Block, South China: Evidence from geochemistry, zircon U-Pb geochronology and Nd-Hf isotopes of a granite-charnockite suite in southwestern Zhejiang (United States)

    Zhao, Lei; Zhou, Xiwen; Zhai, Mingguo; Santosh, M.; Ma, Xudong; Shan, Houxiang; Cui, Xiahong


    The Badu complex and associated Paleoproterozoic granitoids are among the oldest known rocks in the Cathaysia Block in South China. The Paleoproterozoic units of the Badu complex are dominantly composed of metapelitic rocks and meta-greywackes. Here we report LA-SS-ICP-MS (laser ablation-split-stream inductively coupled plasma-mass spectrometry) zircon U-Pb data from a newly discovered garnet-bearing granite which show an emplacement age of 1929 ± 15 Ma and metamorphism at 1872 ± 34 Ma. We also report U-Pb ages of 1886 ± 16 Ma, 1858 ± 7 Ma, 1848 ± 11 Ma from a gneissic granodiorite, and two charnockites respectively. The garnet-bearing granite is peraluminous with A/CNK range from 1.1 to 1.3. The rock shows relatively high SiO2, K2O and Rb contents, and low total REE, Sr, CaO and ferromagnesian components, typical of leucogranites. The whole rock Nd two-stage model age(TDM2(Nd)) of this rock is ca. 2.7 Ga, zircon Hf crustal model ages(TDMC(Hf)) peak at about 2.7 Ga, and abundant inherited zircons occur with U-Pb ages in the range of 2044 to 2803 Ma. Evidences from zircon U-Pb age and Hf isotope compositions, whole rock Nd isotopes and whole rock major and trace elements suggest a metasedimentary protolith, and that the garnet-bearing granite (leucogranite) was derived by partial melting in a thickened crust at about 1.93 Ga. The gneissic granodiorite and charnockites show indistinguishable major and trace element features, as well as zircon Hf and whole rock Nd isotope compositions, indicating that they were generated from the same source rocks. The gneissic granodiorite and charnockites are ferroan, calc-alkalic and metaluminous with A/CNK range from 0.80 to 0.98. They display relatively low SiO2 contents and Ga/Al ratios, suggesting their A-type affinity. Their zircon TDMC(Hf) age-peak is 2.9 Ga and whole rock TDM2(Nd) ages range from 2.8 to 2.9 Ga. These high temperature rocks were generated possibly through the partial melting of ancient amphibolites (2

  18. Isotopic compositions of boron in sediments and their implications

    Digital Repository Service at National Institute of Oceanography (India)

    Shirodkar, P.V.; Yingkai, X.

    of sediments are mostly closer to the boron isotopic composition of minerals. Such low delta sup(11)B values are attributed to the presence of borates, ulexite and other carbonate minerals in sediments of the salt lakes of Qaidam Basin....

  19. Isotopic compositions of the elements 2013 (IUPAC Technical Report) (United States)

    Meija, Juris; Coplen, Tyler B.; Berglund, Michael; Brand, Willi A.; De Bièvre, Paul; Gröning, Manfred; Holden, Norman E.; Irrgeher, Johanna; Loss, Robert D.; Walczyk, Thomas; Prohaska, Thomas


    The Commission on Isotopic Abundances and Atomic Weights ( of the International Union of Pure and Applied Chemistry ( has revised the Table of Isotopic Compositions of the Elements (TICE). The update involved a critical evaluation of the recent published literature. The new TICE 2013 includes evaluated data from the “best measurement” of the isotopic abundances in a single sample, along with a set of representative isotopic abundances and uncertainties that accommodate known variations in normal terrestrial materials.

  20. Geochronological, elemental and Sr-Nd-Hf-O isotopic constraints on the petrogenesis of the Triassic post-collisional granitic rocks in NW Thailand and its Paleotethyan implications (United States)

    Wang, Yuejun; He, Huiying; Cawood, Peter A.; Srithai, Boontarika; Feng, Qinglai; Fan, Weiming; Zhang, Yuzhi; Qian, Xin


    New U-Pb geochronological, petrologic, elemental and Sr-Nd-Hf-O isotopic data for the granites from the Inthanon and Sukhothai zones in NW Thailand in conjunction with correlations with SW China are presented to constrain the age and position of the Paleotethys Ocean in this region and the associated assembly of Southeast Asia. The geochronological data show that the granitic rocks in the Inthanon and Sukhothai zones, herein named Group 1 and Group 2 granites, respectively, yield similar crystallization ages of 230-200 Ma. Group 1 samples are characterized by monzogranite and granite with I- and S-type geochemical affinity and Group 2 samples by I-type monzogranite and granodiorite. They have generally similar chondrite-normalized REE and PM-normalized multi-element patterns but distinct Sr-Nd-Hf-O isotopic compositions. Group 1 samples have slightly higher initial 87Sr/86Sr ratios (0.7111-0.7293) but lower εNd(t) values (- 11.1 to - 14.1) than those of Group 2 samples (87Sr/86Sr(i) = 0.7073-0.7278 and εNd(t) = - 8.3 to - 11.0). Group 1 samples show the lower εHf(t) values (- 5.4 to - 18.2), older TDM (1.62-2.40 Ga) and higher δ18O values (+ 7.95 to + 9.94) than those of Group 2 samples (εHf(t) of - 11.1 to + 4.80, TDM of 0.96-1.95 Ga and δ18O of + 4.95 to + 7.98) for the Triassic crystallization zircons. These geochemical signatures are similar to the Kwangsian and Indosinian granites in the South China and Indochina blocks but distinct from those of the Gangdese I-type granite and Sibumasu Paleozoic granite. Our data suggest that Group 1 samples mainly originated from the early Paleozoic supracrustal rocks containing metapelite and metavolcanic components, which had previously experienced the surface weathering. Group 2 samples were derived from a hybridized source of an old metamorphic and a newly underplated mafic component. Synthesis of our data with available regional observations indicates that the Inthanon zone represents the main suture zone of the

  1. Oxygen isotopic composition of carbon dioxide in the middle atmosphere


    Liang, Mao-Chang; Blake, Geoffrey A.; Lewis, Brenton R.; Yung, Yuk L.


    The isotopic composition of long-lived trace molecules provides a window into atmospheric transport and chemistry. Carbon dioxide is a particularly powerful tracer, because its abundance remains >100 parts per million by volume (ppmv) in the mesosphere. Here, we successfully reproduce the isotopic composition of CO2 in the middle atmosphere, which has not been previously reported. The mass-independent fractionation of oxygen in CO2 can be satisfactorily explained by the exchange reaction with...

  2. Grenvillian orogeny in the Southern Cathaysia Block: Constraints from U-Pb ages and Lu-Hf isotopes in zircon from metamorphic basement

    Institute of Scientific and Technical Information of China (English)

    WANG LiJuan; YU JinHai; S.Y. O'REILLY; W.L. GRIFFIN; SUN Tao; WEI ZhenYang; JIANG ShaoYong; SHU LiangShu


    Metamorphic basement rocks in the Cathaysia Block are composed mainly of meta-sediments with different ages. New zircon U-Pb geochronological results from the meta-sedimentary rocks exposed in the Zengcheng and Hezi areas, southern Cathaysia Block, show that they consist dominantly of early Neoproterozoic (1.0-0.9 Ga) materials with minor Paleo- to Mesoproterozoic and late Neoproterozoic (0.8-0.6 Ga) components, suggesting that the detritus mostly come from a Grenvillian orogen. The youngest detrital zircon ages place a constraint on the deposition time of these sediments in Late Neoproterozoic. Zircon Hf isotopic compositions indicate that the Grenvillian zircons were derived from the reworking of Mesoproterozoic arc magmatic rocks and Paleoproterozoic continental crust, implying an arc-continent collisional setting. Single-peak age spectra and the presence of abundant euhedral Grenvillian zircons suggest that the sedimentary provenance is not far away from the sample location. Thus, the Grenvillian orogen probably preexisted along the southern margin of the Cathaysia Block, or very close to the south. Similarity in the ages of Grenvillian orogeny and the influence of the assembly of Gondwana in South China with India and East Antarctic are discussed, with suggestion that South China was more likely linked with the India-East Antarctica continents in Early Neoproterozoic rather than between western Laurentia and eastern Australia.

  3. Cretaceous seamounts along the continent ocean transition of the Iberian margin: U Pb ages and Pb Sr Hf isotopes (United States)

    Merle, Renaud; Schärer, Urs; Girardeau, Jacques; Cornen, Guy


    To elucidate the age and origin of seamounts in the eastern North Atlantic, 54 titanite and 10 zircon fractions were dated by the U-Pb chronometer, and initial Pb, Sr, and Hf isotope ratios were measured in feldspars and zircon, respectively. Rocks analyzed are essentially trachy-andesites and trachytes dredged during the "Tore Madeira" cruise of the Atalante in 2001. The ages reveal different pulses of alkaline magmatism occurring at 104.4 ± 1.4 (2 σ) Ma and 102.8 ± 0.7 Ma on the Sponge Bob seamount, at 96.3 ± 1.0 Ma on Ashton seamount, at 92.3 ± 3.8 Ma on the Gago Coutinho seamount, at 89.3 ± 2.3 Ma and 86.5 ± 3.4 Ma on the Jo Sister volcanic complex, and at 88.3 ± 3.3 Ma, 88.2 ± 3.9, and 80.5 ± 0.9 Ma on the Tore locality. No space-time correlation is observed for alkaline volcanism in the northern section of the Tore-Madeira Rise, which occurred 20-30 m.y. after opening of the eastern North Atlantic. Initial isotope signatures are: 19.139-19.620 for 206Pb/ 204Pb, 15.544-15.828 for 207Pb/ 204Pb, 38.750-39.936 for 208Pb/ 204Pb, 0.70231-0.70340 for 87Sr/ 86Sr, and +6.9 to +12.9 for initial epsilon Hf. These signatures are different from Atlantic MORB, the Madeira Archipelago and the Azores, but they lie in the field of worldwide OIB. The Cretaceous seamounts therefore seem to be generated by melts from a OIB-type source that interact with continental lithospheric mantle lying formerly beneath Iberia and presently within the ocean-continent transition zone. Inheritance in zircon and high 207Pb of initial Pb substantiate the presence of very minor amounts of continental material in the lithospheric mantle. A long-lived thermal anomaly is the most plausible explanation for alkaline magmatism since 104 Ma and it could well be that the same anomaly is still the driving force for tertiary and quaternary alkaline magmatism in the eastern North Atlantic region. This hypothesis is agreement with the plate-tectonic position of the region since Cretaceous time

  4. A first roadmap for kryptology. [isotopic composition from supernovae (United States)

    Heymann, D.; Dziczkaniec, M.


    Studies of the complex variations of the isotopic composition of xenon in the solar system have been christened 'xenology'. In the title of the present investigation, the word 'kryptology' is employed to indicate the primary objective of the reported studies. This objective is related to the prediction of the isotopic composition of krypton which comes from a number of specific locations of a supernova in association with the isotopic compositions of xenon from these locations. Krypton is a logical candidate for testing the stellar theory on geochemical grounds, taking into account also the point of view of nucleosynthesis, because the isotopes of xenon and krypton are formed by the same thermonuclear processes in stars. The data and arguments presented in the investigation show that the treatment by Heymann and Dziczkaniec (1979), although not wrong, is too simplistic, because it has ignored the possibility of holdup and arrest in Xe network.

  5. 甘肃敦煌水峡口地区前寒武纪岩石的锆石U-Pb年龄、Hf同位素组成及其地质意义%Zircon geochronology and Lu-Hf isotope compositions for Precambrian rocks of the Dunhuang complex in Shuixiakou area, Gansu Province

    Institute of Scientific and Technical Information of China (English)

    赵燕; 第五春荣; 孙勇; 朱涛; 王洪亮


    Dunhuang block is located in the southeast of Tarim Craton,and the research of Precambrian Dunhuang complex is of great significance in investigating the formation and evolution of the crust of Dunhuang block,as well as its tectonic relationship with the North China Craton and Yangtze Craton.Dunhuang complex,in Shuixiakou area,Gansu Province,mainly consists of tonaliticgranodioritic gneisses,granitic gneisses and metamorphosed supracrustal rocks.The age of 2561 ± 16Ma and 2510 ± 22Ma respectively for the tonalitic and the granitic gneisses by LA-ICP-MS U-Pb dating of zircons confirm the existence of Archean rocks in Dunhuang complex,LA-ICP-MS U-Pb dating of zircons yielded a metamorphic age of 1806-± 14Ma for the amphibolite,and its parent magma probably derived from the partial melting of ancient lithospheric mantle.Based on the integration of our study and the available data,we put forward that Dunhuang complex has experienced a metamorphism during the Late Paleoproterozoic (1.80 ~ 1.85Ga).The analysis of Hf isotopes of zircons indicates that ~ 2.5Ga is a major period of crustal growth in Dunhuang block during the Neoarchean,while the ~ 1.8Ga tectonic-thermal event represent a reworking period of ancient crust.The above data show that the formation and evolution of Dunhuang block is similar with the North China Craton during Early Precambrian,and they are involved in the global collision-orogenic event during Columbia Period.%敦煌杂岩位于塔里木克拉通的东部,探寻和研究其中的早前寒武纪地质体对于探讨敦煌地块早前寒武纪地壳的形成和演化及其构造归属等问题具有重要的意义.甘肃敦煌水峡口地区的敦煌杂岩主要由英云闪长质片麻岩、花岗闪长质片麻岩以及表壳岩石组成.利用LA-ICP-MS锆石U-Pb定年方法测得水峡口英云闪长片麻岩和花岗片麻岩原岩的形成年龄分别为2561±16Ma和2510±22Ma,确证了在敦煌杂岩中存在太古宙岩石.此外,还

  6. Genesis and open-system evolution of Quaternary magmas beneath southeastern margin of Tibet: Constraints from Sr-Nd-Pb-Hf isotope systematics (United States)

    Zou, Haibo; Ma, Mingjia; Fan, Qicheng; Xu, Bei; Li, Shuang-Qing; Zhao, Yongwei; King, David T.


    Post-collisional volcanic rocks on the Tibetan Plateau and its margins contain valuable information about the geodynamic processes associated with this Cenozoic continent-continent collision. The Quaternary Tengchong volcanic field at the southeastern margin of the Tibetan Plateau formed high-potassium calc-alkaline volcanic rocks. Herein, we present comprehensive Nd-Sr-Pb-Hf isotopic and elemental data for trachybasalts, basaltic trachyandesites, and trachyandesites from four Quaternary Tengchong volcanoes (Maanshan, Dayingshan, Heikongshan, and Laoguipo) in order to understand their magma genesis and evolution as well as tectonic significance. Good correlations between SiO2 content and the ratios 87Sr/86Sr, 143Nd/144Nd, 206Pb/204Pb, and 177Hf/176Hf for these Quaternary volcanics strongly suggest that the combined assimilation and fractional crystallization (AFC) was an important process in the origin of basaltic trachyandesites and trachyandesites. High Y and Yb contents and low Sr/Y ratios of these basaltic trachyandesites and trachyandesites are uncharacteristic of adakites that formed by partial melting of eclogitic lower crust or partial melting of basaltic oceanic crust with eclogite as a restite. A combined assimilation-fractional crystallization model is proposed for these basaltic trachyandesites and trachyandesites. Nd-Sr-Pb-Hf isotopes for the uncontaminated Tengchong magma (trachybasalts with SiO2 5.5% wt.%) reflect a heterogeneous enriched mantle source. High Th/U, Th/Ta, and Rb/Nb ratios and Nd-Sr-Pb-Hf isotope characteristics of the uncontaminated magmas suggest that the enriched mantle beneath Tengchong formed as a result of subduction of clay-rich sediments, which probably came from the Indian continental plate. Partial melting of the enriched mantle was generated by deep continental subduction coupled with recent regional extension in the Tengchong area.

  7. Hf isotope study of Palaeozoic metaigneous rocks of La pampa province and implications for the occurrence of juvenile early Neoproterozoic (Tonian) magmatism in south-central Argentina (United States)

    Chernicoff, C. J.; Zappettini, E. O.; Santos, J. O. S.; Belousova, E.; McNaughton, N. J.


    On a global scale, juvenile Tonian (Early Neoproterozoic) magmatic rocks are associated with the extensional events that lead to the breakup of the Rodinia supercontinent. In Argentina, no geological record is available for this time interval, lasting from 1000 to 850 Ma. We present indirect evidence for the existence of Tonian extension in Argentina, as supported by Hf and Nd isotope determinations on Phanerozoic magmatic and sedimentary rocks. We mainly focus on our own Hf isotope determinations carried out on U-Pb SHRIMP dated zircons from Palaeozoic metaigneous rocks of La Pampa province, south-central Argentina, i.e. metagabbros of Valle Daza, dioritic orthogneiss of Estancia Lote 8, and metadiorite of Estancia El Carancho, having found that these rocks were derived from sources of ca. 920 to ca 880 Ma, with ɛHf values between +6.83 and + 9.59. Inherited zircons of this age and character identified in these rocks also point to the same source. We also compile additional Hf and Nd studies from previous work on Phanerozoic magmatic and sedimentary rocks. We preliminarily compare the age of the juvenile Tonian sources referred to in our work with that of two extensional events identified in the São Francisco craton, Brazil.

  8. A Sr-Nd-Hf isotope characterization of dust source areas in Victoria Land and the McMurdo Sound sector of Antarctica (United States)

    Blakowski, Molly A.; Aciego, Sarah M.; Delmonte, Barbara; Baroni, Carlo; Salvatore, Maria Cristina; Sims, Kenneth W. W.


    Determining the geographical provenance of dust provides crucial insight into the global dust cycle. For the East Antarctic Ice Sheet (EAIS), the importance of Southern hemisphere potential dust sources has been thoroughly investigated using radiogenic isotopes, whereas proximal dust source areas located on the periphery of the ice sheet remain poorly documented from a geochemical standpoint. In this work, we expand the existing isotopic (Srsbnd Nd) catalogue of dust and sand-sized sediments from Victoria Land and the McMurdo Sound sector, and incorporate Hf isotopic data to place additional constraints on dust source identification. The isotopic field for materials considered in this study is characterized by 87Sr/86Sr ratios ranging from 0.703 to 0.783, εNd between -12.01 and 6.36, and εHf from -16.77 to 6.89. As reported in previous works, the data reveal close relationships between Antarctic sediments and distinct parent lithologies; in addition, our findings emphasize the background presence of very fine dusts originating from dominant global sources and regional volcanic activity as barriers to direct source-to-sink comparison of isotopic signatures. Thus, geochemical characterizations of dust sources to the Antarctic ice sheet involving multiple size fractions, including coarser-grained particles more susceptible to short-range transport, can help us to rule out global sources of dust when examining local sediment cores and ice cores.

  9. The ruthenium isotopic composition of the oceanic mantle (United States)

    Bermingham, K. R.; Walker, R. J.


    The approximately chondritic relative, and comparatively high absolute mantle abundances of the highly siderophile elements (HSE), suggest that their concentrations in the bulk silicate Earth were primarily established during a final ∼0.5 to 1% of ;late accretion; to the mantle, following the cessation of core segregation. Consequently, the isotopic composition of the HSE Ru in the mantle reflects an amalgamation of the isotopic compositions of late accretionary contributions to the silicate portion of the Earth. Among cosmochemical materials, Ru is characterized by considerable mass-independent isotopic variability, making it a powerful genetic tracer of Earth's late accretionary building blocks. To define the Ru isotopic composition of the oceanic mantle, the largest portion of the accessible mantle, we report Ru isotopic data for materials from one Archean and seven Phanerozoic oceanic mantle domains. A sample from a continental lithospheric mantle domain is also examined. All samples have identical Ru isotopic compositions, within analytical uncertainties, indicating that Ru isotopes are well mixed in the oceanic mantle, defining a μ100Ru value of 1.2 ± 7.2 (2SD). The only known meteorites with the same Ru isotopic composition are enstatite chondrites and, when corrected for the effects of cosmic ray exposure, members of the Main Group and sLL subgroup of the IAB iron meteorite complex which have a collective CRE corrected μ100Ru value of 0.9 ± 3.0. This suggests that materials from the region(s) of the solar nebula sampled by these meteorites likely contributed the dominant portion of late accreted materials to Earth's mantle.

  10. Calcium isotopic compositions of mid-ocean ridge basalts (United States)

    Zhu, H.; Zhang, Z.; Sun, W.; Wang, G. Q.


    Previous studies have demonstrated that Earth's mantle has heterogeneous calcium isotopic compositions. But the reason why mantle has its heterogeneity remains uncertain. In general, δ44/40Ca values of mantle xenolith samples have a variation of >0.45‰. While ultramafic rocks, especially dunites, have higher δ44/40Ca values than volcanic rocks, and there is a positive correlation between δ44/40Ca and Ca/Mg. These phenomena imply that the heterogeneity of Ca isotopic compositions of mantle xenolith samples might result from different degrees of melt extraction, as indicated by large Ca isotopic fractionation between co-existing clinopyroxene and orthopyroxene. However, because ancient marine carbonate has its own unique calcium isotopic characteristics, recycling of even a small amount of ancient marine carbonates into the mantle could also cause the heterogeneity of Ca isotopes in Earth's mantle. This could be the reason why oceanic island basalts (OIB) have lighter Ca isotopic compositions than the mantle xenolith. Thus, the lighter Ca isotopic compositions in the mantle source cannot only be ascribed to magmatic processes. Therefore, it is more important to know calcium isotopic characteristics during partial melting and oceanic crust contamination.Mid-ocean ridge basalts (MORB) are formed from the partial melts of the upper mantle and are rarely affected by crustal contamination. Different types of MORB, including D-MORB, N-MORB and E-MORB, have experienced different degrees of partial melting and contamination of enriched end-members. Here we report calcium isotopic characteristic of different types of MORB, we believe it will be very helpful to understand the behaviors of Ca isotopes during partial melting and it is possible to provide further information to discover the reason why calcium isotopic compositions is heterogeneous in Earth's mantle. This work was supported by Natural Science Foundation of China (No. 41373007, No. 41490632 and No. 91328204

  11. Isotopic compositions of cometary matter returned by Stardust. (United States)

    McKeegan, Kevin D; Aléon, Jerome; Bradley, John; Brownlee, Donald; Busemann, Henner; Butterworth, Anna; Chaussidon, Marc; Fallon, Stewart; Floss, Christine; Gilmour, Jamie; Gounelle, Matthieu; Graham, Giles; Guan, Yunbin; Heck, Philipp R; Hoppe, Peter; Hutcheon, Ian D; Huth, Joachim; Ishii, Hope; Ito, Motoo; Jacobsen, Stein B; Kearsley, Anton; Leshin, Laurie A; Liu, Ming-Chang; Lyon, Ian; Marhas, Kuljeet; Marty, Bernard; Matrajt, Graciela; Meibom, Anders; Messenger, Scott; Mostefaoui, Smail; Mukhopadhyay, Sujoy; Nakamura-Messenger, Keiko; Nittler, Larry; Palma, Russ; Pepin, Robert O; Papanastassiou, Dimitri A; Robert, François; Schlutter, Dennis; Snead, Christopher J; Stadermann, Frank J; Stroud, Rhonda; Tsou, Peter; Westphal, Andrew; Young, Edward D; Ziegler, Karen; Zimmermann, Laurent; Zinner, Ernst


    Hydrogen, carbon, nitrogen, and oxygen isotopic compositions are heterogeneous among comet 81P/Wild 2 particle fragments; however, extreme isotopic anomalies are rare, indicating that the comet is not a pristine aggregate of presolar materials. Nonterrestrial nitrogen and neon isotope ratios suggest that indigenous organic matter and highly volatile materials were successfully collected. Except for a single (17)O-enriched circumstellar stardust grain, silicate and oxide minerals have oxygen isotopic compositions consistent with solar system origin. One refractory grain is (16)O-enriched, like refractory inclusions in meteorites, suggesting that Wild 2 contains material formed at high temperature in the inner solar system and transported to the Kuiper belt before comet accretion.

  12. Geochemistry and oxygen isotope composition of main-group pallasites and olivine-rich clasts in mesosiderites

    DEFF Research Database (Denmark)

    Greenwood, Richard C.; Barrat, Jean-Alix; Scott, Edward R. D.


    they are not. To investigate this "Great DuniteShortage" we have undertaken a geochemical and oxygen isotope study of main-group pallasites and dunitic rocks from mesosiderites.Oxygen isotope analysis of 24 main-group pallasites (103 replicates) yielded a mean Δ17O value of -0.187 ±0.016‰ (2σ), which is fully...... origin. Although the Dawn mission did not detect mesosiderite-like material on Vesta, evidence linking the mesosiderites and HEDs includes: (i) theirnearly identical oxygen isotope compositions; (ii) the presence in both of coarse-grained Mg-rich olivines; (iii) both have synchronous Lu-Hf and Mn-Cr ages...... asteroidsand meteorites results from a range of factors. However, evidence from pallasites and mesosiderites indicates that the most important reason for this olivine shortage lies in the early, catastrophic destruction ofplanetesimals in the terrestrial planet-forming region and the subsequent preferential...

  13. Zinc isotope fractionation during magmatic differentiation and the isotopic composition of the bulk Earth (United States)

    Chen, Heng; Savage, Paul S.; Teng, Fang-Zehn; Helz, Rosalind T.; Moynier, Frédéric


    he zinc stable isotope system has been successfully applied to many and varied fields in geochemistry, but to date it is still not completely clear how this isotope system is affected by igneous processes. In order to evaluate the potential application of Zn isotopes as a proxy for planetary differentiation and volatile history, it is important to constrain the magnitude of Zn isotopic fractionation induced by magmatic differentiation. In this study we present high-precision Zn isotope analyses of two sets of chemically diverse, cogenetic samples from Kilauea Iki lava lake, Hawaii, and Hekla volcano, Iceland, which both show clear evidence of having undergone variable and significant degrees of magmatic differentiation. The Kilauea Iki samples display small but resolvable variations in Zn isotope composition (0.26‰66Zn66Zn defined as the per mille deviation of a sample's 66Zn/64Zn compositional ratio from the JMC-Lyon standard), with the most differentiated lithologies exhibiting more positive δ66Zn values. This fractionation is likely a result of the crystallization of olivine and/or Fe–Ti oxides, which can both host Zn in their crystal structures. Samples from Hekla have a similar range of isotopic variation (0.22‰66Zn66Zn=0.28±0.05‰ (2s.d.).

  14. Iron isotope composition of some Archean and Proterozoic iron formations (United States)

    Planavsky, Noah; Rouxel, Olivier J.; Bekker, Andrey; Hofmann, Axel; Little, Crispin T. S.; Lyons, Timothy W.


    Fe isotopes can provide new insight into redox-dependent biogeochemical processes. Precambrian iron formations (IF) are deserving targets for Fe isotope studies because they are composed predominantly of authigenic Fe phases and record a period of unprecedented iron deposition in Earth's history. We present Fe isotope data for bulk samples from 24 Archean and Proterozoic IF and eight Phanerozoic Fe oxide-rich deposits. These data reveal that many Archean and early Paleoproterozoic iron formations were a sink for isotopically heavy Fe, in contrast to later Proterozoic and Phanerozoic Fe oxide-rich rocks. The positive δ56Fe values in IF are best explained by delivery of particulate ferric oxides formed in the water column to the sediment-water interface. Because IF are a net sink for isotopically heavy Fe, there must be a corresponding pool of isotopically light Fe in the sedimentary record. Earlier work suggested that Archean pyritic black shales were an important part of this light sink before 2.35 billion years ago (Ga). It is therefore likely that the persistently and anomalously low δ56Fe values in shales are linked with the deposition of isotopically heavy Fe in IF in the deeper parts of basins. IF deposition produced a residual isotopically light dissolved Fe pool that was captured by pyritic Fe in shales. Local dissimilatory Fe reduction in porewater and associated diagenetic reactions resulting in pyrite and carbonate precipitation may have further enhanced Fe isotope heterogeneity in marine sediments, and an 'iron shuttle' may have transported isotopically light Fe from shelf sediments to the basin. Nevertheless, water-column processing of hydrothermally delivered Fe likely had the strongest influence on the bulk iron isotope composition of Archean and Paleoproterozoic iron formations and other marine sediments.

  15. Soil Carbon: Compositional and Isotopic Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Moran, James J.; Alexander, M. L.; Laskin, Alexander


    This is a short chapter to be included in the next edition of the Encyclopedia of Soil Science. The work here describes techniques being developed at PNNL for investigating organic carbon in soils. Techniques discussed include: laser ablation isotope ratio mass spectrometry, laser ablation aerosol mass spectrometry, and nanospray desorption electrospray ionization mass spectrometry.

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

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


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

  17. Influx of Different Galapagos Plume Components to the Galapagos Spreading Center: Evidence From Sr-Nd-Pb-Hf Isotope Variations in Axial Lavas Between 86W and 92.5W (United States)

    Hauff, F.; Hanan, B.; Hoernle, K. A.; Kokfelt, T. F.; Christie, D.; Werner, R.


    We present new Sr-Nd-Pb-Hf isotope data of basaltic glasses from the GSC between 86W and 92.5W. In this part of the ridge the main structural inventory includes an overlapping spreading center (OSC) at 87.3W, a transform fault (TF) at 91W and a series of seamount chains intersecting the GSC West of the 91W TF. The systematic transition from an axial-valley and rift morphology at axial depths of 2450 m.b.s.l. in the 86W area to an axial-high morphology at progressively shallower depths of 1500 m.b.s.l in the 90.5W area together with gradational changes in major and trace element chemistry of the axial lavas is believed to reflect increasing mantle temperature and compositional changes related to the Galapagos plume [1]. Previous work from 83W to 105W revealed a broad symmetric gradational pattern at around 91W and lead to the conclusion that this region is the main point of plume influx on the GSC [2]. Based on published isotope data Christie et al. (2005) inferred the probable existence of two enrichment peaks immediately East and West of the 91TF. Indeed, along axis variations of our new Sr-Nd-Pb-Hf isotope data map two distinct peaks of enrichment at 92W and 90.5W, suggesting that mantle from the Galapagos hotspot enters the GSC melting zone on both sides of the 91W transform fault. Lavas from within the 91W TF are isotopically intermediate and show a distinct depletion in incompatible trace elements, which may reflect repeated melting at shallow depth of passively upwelling mantle in this unique extensional regime. At least three different components are required to generate the observed isotope correlations. When compared to the geographically distinct isotopic domains of the Galapagos islands; GSC lavas East of the 91W TF form tight correlations from the rim of the Central Galapagos domain through the Eastern Galapagos domain towards DMM. Most axial lavas and corresponding off axis seamounts West of the 91W TF have higher 87Sr/86Sr, 207Pb/204Pb, 208Pb/204Pb

  18. Zircon Dating,Hf Isotope Composition,Geochemistry and Their Prospecting Signification of the Langqiao Intrusion in Jingxian County,South Anhui Province%皖南泾县榔桥岩体锆石U-Pb定年、Hf同位素和地球化学特征及其找矿指示意义

    Institute of Scientific and Technical Information of China (English)

    李双; 杨晓勇; 孙卫东; 戴圣潜


    The Langqiao granodiorite intrusion is a complex pluton with melted crust-mantle materials,located in the northern margin of the fold belt in Jingxian county of South Anhui province.The U-Pb dating results for zircons from two granodiorite samples formed in main forming stage of the Langqiao intrusion and one porphyry granite samples from the vein rock formed at the later forming stage yielded weight average ages of 135. 6±1. 8Ma,137. 6 ±2. 0Ma,136. 4 ±1. 9Ma,respectively,indicating the intrusion formed in the Early Cretaceous.The zircon Hf isotopic analysis suggested that this intrusion was formed by partial melting of Mesoproterozoic crustal materials,contaminated by a small amount of Paleo-proterozoic crutal materials.The “zircon saturation temperature”calculated by whole-rock Zr contents show the magmatic crystallization temperature of Langqiao granodiorite intrusion and porphyry granite from vein rock is 749~781℃,722~745℃,respectively,indicating rapid cooling history of magma;the element geochemical studies show that the intrusion formed accompanied with fractional crystallization of plagioclase, K-feldspar and the accessory minerals,such as apatite,ilmenite.Zircon Ce(Ⅳ)/Ce(Ⅲ)ratios suggest the high oxygen fugacity in the magmatic process is conducive the Cu-Au mineralization,while the fractional crystallization of plagioclase reduced EuN/EuN* to 0. 2~0. 4 .The Langqiao intrusion is enriched in large-ion lithophile elements,Pb,depleted in high field strength elements (Nb,Ta,Zr,Ti),also has obvious differentiation between LREE and HREE,with more enriched LREE than HREE,similar to the arc magmatic rock;tectonic setting discrimination diagrams suggested the formation of Langqiao intrusion was closely related to the subduction and collision of the Paleo-pacific plate towards the Euroasian continent.%安徽泾县榔桥花岗闪长岩体为分布于皖南台褶带北缘壳幔同熔型复式岩体。该岩体主侵入期两个花岗闪长岩样品和

  19. Stable isotope composition of human fingernails from Slovakia

    Energy Technology Data Exchange (ETDEWEB)

    Grolmusová, Zuzana, E-mail: [Comenius University in Bratislava, Faculty of Mathematics, Physics and Informatics, Department of Experimental Physics, Mlynská dolina F2, 842 48 Bratislava (Slovakia); State Geological Institute of Dionýz Štúr, Laboratory of Isotope Geology, Mlynská dolina 1, 817 04 Bratislava (Slovakia); Rapčanová, Anna [Comenius University in Bratislava, Faculty of Mathematics, Physics and Informatics, Department of Experimental Physics, Mlynská dolina F2, 842 48 Bratislava (Slovakia); Michalko, Juraj; Čech, Peter [State Geological Institute of Dionýz Štúr, Laboratory of Isotope Geology, Mlynská dolina 1, 817 04 Bratislava (Slovakia); Veis, Pavel [Comenius University in Bratislava, Faculty of Mathematics, Physics and Informatics, Department of Experimental Physics, Mlynská dolina F2, 842 48 Bratislava (Slovakia); State Geological Institute of Dionýz Štúr, Laboratory of Isotope Geology, Mlynská dolina 1, 817 04 Bratislava (Slovakia)


    Stable isotope composition of human fingernails has proven to be useful for documenting human dietary information and geographical patterns in archeological, forensic, anthropological and biological studies. Therefore, it is of interest to detect all factors influencing the stable isotopic composition in the certain regions in the world. Carbon and nitrogen isotope data of human fingernail keratin from 52 individuals from Slovakia were reported in this study. The online combustion and continuous flow isotope-ratio mass spectrometer Delta V Advantage was used for δ{sup 13}C and δ{sup 15}N analysis of fingernail keratin samples from 24 vegetarian and 28 omnivorous individuals. A group of people with frequent meat consumption showed enrichment in {sup 13}C and {sup 15}N isotopes in fingernails. A similar trend was observed with increasing seafood in an individual's diet. Moreover a significant difference was revealed between smokers and nonsmokers for both δ{sup 13}C and δ{sup 15}N values. These data were compared to previously published δ{sup 13}C and δ{sup 15}N fingernail values from across the globe. This study brings new information on the stable isotope signature of individuals from Slovakia and characterizes the Central European region for the first time. The stable isotope composition of fingernails is influenced by the frequency of meat and seafood consumption as well as smoking. - Highlights: • This study deals with stable isotope analyses of fingernails from Slovak volunteers. • δ{sup 13}C and δ{sup 15}N values of vegetarian and omnivore fingernails were compared. • Influence of sex, diet and smoking was studied.

  20. Sr and Nd isotopic and trace element compositions of Quaternary volcanic centers of the Southern Andes (United States)

    Futa, K.; Stern, C.R.


    Isotopic compositions of samples from six Quaternary volcanoes located in the northern and southern extremities of the Southern Volcanic Zone (SVZ, 33-46??S) of the Andes and from four centers in the Austral Volcanic Zone (AVZ, 49-54??S) range for 87Sr 86Sr from 0.70280 to 0.70591 and for 143Nd 144Nd from 0.51314 to 0.51255. The ranges are significantly greater than previously reported from the southern Andes but are different from the isotopic compositions of volcanoes in the central and northern Andes. Basalts and basaltic andesites from three centers just north of the Chile Rise-Trench triple junction have 87Sr 86Sr, 143Nd 144Nd, La Yb, Ba La, and Hf Lu that lie within the relatively restricted ranges of the basic magmas erupted from the volcanic centers as far north as 35??S in the SVZ of the Andes. The trace element and Sr and Nd isotopic characteristics of these magmas may be explained by source region contamination of subarc asthenosphere, with contaminants derived from subducted pelagic sediments and seawater-altered basalts by dehydration of subducted oceanic lithosphere. In the northern extremity of the SVZ between 33?? and 34??S, basaltic andesites and andesites have higher 87Sr 86Sr, Rb Cs, and Hf Lu, and lower 143Nd 144Nd than basalts and basaltic andesites erupted farther south in the SVZ, which suggests involvement of components derived from the continental crust. In the AVZ, the most primitive sample, high-Mg andesite from the southernmost volcanic center in the Andes (54??S) has Sr and Nd isotopic compositions and K Rb and Ba La similar to MORB. The high La Yb of this sample suggests formation by small degrees of partial melting of subducted MORB with garnet as a residue. Samples from centers farther north in the AVZ show a regionally regular northward increase in SiO2, K2O, Rb, Ba, Ba La, and 87Sr 86Sr and decrease in MgO, Sr, K Rb, Rb Cs, and 143Nd 144Nd, suggesting increasingly greater degrees of fractional crystallization and associated intra

  1. Aerosol carbon isotope composition over Baltic Sea (United States)

    Garbaras, Andrius; Pabedinskas, Algirdas; Masalaite, Agne; Petelski, Tomasz; Gorokhova, Elena; Sapolaite, Justina; Ezerinskis, Zilvinas; Remeikis, Vidmantas


    Particulate carbonaceous matter is significant contributor to ambient particulate matter originating from intervening sources which contribution is difficult to quantify due to source diversity, chemical complexity and processes during atmospheric transport. Carbon isotope analysis can be extremely useful in source apportionment of organic matter due to the unique isotopic signatures associated with anthropocentric (fossil fuel), continental (terrestrial plants) and marine sources, and is particularly effective when these sources are mixed (Ceburnis et al., 2011;Ceburnis et al., 2016). We will present the isotope ratio measurement results of aerosol collected during the cruise in the Baltic Sea. Sampling campaign of PM10 and size segregated aerosol particles was performed on the R/V "Oceania" in October 2015. Air mass back trajectories were prevailing both from the continental and marine areas during the sampling period. The total carbon concentration varied from 1 µg/m3 to 8 µg/m3. Two end members (δ13C = -25‰ and δ13C = -28 ‰ ) were established from the total stable carbon isotope analysis in PM10 fraction. δ13C analysis in size segregated aerosol particles revealed δ13C values being highest in the 1 - 2.5 µm range (δ13C = -24.9 ‰ ) during continental transport, while lowest TC δ13C values (δ13C ≈ -27 ‰ ) were detected in the size range D50 dual carbon pools contributing to organic matter enrichment in marine aerosol, Scientific Reports, 6, 2016. Masalaite, A., Remeikis, V., Garbaras, A., Dudoitis, V., Ulevicius, V., and Ceburnis, D.: Elucidating carbonaceous aerosol sources by the stable carbon δ13C TC ratio in size-segregated particles, Atmospheric Research, 158, 1-12, 2015.

  2. Carbon isotopic composition of individual Precambrian microfossils. (United States)

    House, C H; Schopf, J W; McKeegan, K D; Coath, C D; Harrison, T M; Stetter, K O


    Ion microprobe measurements of carbon isotope ratios were made in 30 specimens representing six fossil genera of microorganisms petrified in stromatolitic chert from the approximately 850 Ma Bitter Springs Formation, Australia, and the approximately 2100 Ma Gunflint Formation, Canada. The delta 13C(PDB) values from individual microfossils of the Bitter Springs Formation ranged from -21.3 +/- 1.7% to -31.9 +/- 1.2% and the delta 13C(PDB) values from microfossils of the Gunflint Formation ranged from -32.4 +/- 0.7% to -45.4 +/- 1.2%. With the exception of two highly 13C-depleted Gunflint microfossils, the results generally yield values consistent with carbon fixation via either the Calvin cycle or the acetyl-CoA pathway. However, the isotopic results are not consistent with the degree of fractionation expected from either the 3-hydroxypropionate cycle or the reductive tricarboxylic acid cycle, suggesting that the microfossils studied did not use either of these pathways for carbon fixation. The morphologies of the microfossils suggest an affinity to the cyanobacteria, and our carbon isotopic data are consistent with this assignment.

  3. U-Pb Age and Hf Isotope Study of Detrital Zircons from the Wanzi Supracrustals: Constraints on the Tectonic Setting and Evolution of the Fuping Complex, Trans-North China Orogen

    Institute of Scientific and Technical Information of China (English)

    Xiaoping XIA; Min SUN; Guochun ZHAO; WU Fuyuan; XU Ping; Jian ZHANG; Yanhong HE; ZHANG Jiheng


    Located in the middle segment of the Trans-North China Orogen, the Fuping Complex is considered as a critical area in understanding the evolution history of the North China Craton (NCC).The complex is composed of various high-grade and multiply deformed rocks, including gray gneiss,basic granulite, amphibolite, fine-grained gneiss and marble, metamorphosed to upper amphibolite or granulite facies. It can be divided into four rock units: the Fuping TTG gneisses, Longquanguan augen gneisses, Wanzi supracrustals, and Nanying granitic gneisses. U-Pb age and Hf isotope compositions of about 200 detrital zircons from the Wanzi supracrustals of the Fuping Complex have been analyzed.The data on metamorphic zircon rims give ages of 1.82-1.84 Ga, corresponding to the final amalgamation event of the NCC, whereas the data for igneous zircon cores yield two age populations at ~2.10 and ~2.51 Ga, with some inherited ages scattering between 2.5 and 2.9 Ga. These results suggest that the Wanzi supracrustals were derived from the Fuping TTG gneisses (~2.5 Ga) and the Nanying granitic gneisses (2.0-2.1 Ga) and deposited between 2.10 and 1.84 Ga. All zircons with ~2.51 Ga age have positive initial εHf values from +1.4 to +10.9, suggesting an important crustal growth event at ~2.5 Ga through the addition of juvenile materials from the mantle. The Hf isotope data for the detrital zircons further imply that the 2.8 Ga rocks are important components in the lower crust, which is consistent with a suggestion from Nd isotope data for the Eastern Block. The zircons of 2.10 Ga population have initial εHf values of-4.9 to +6.1, interpreted as mixing of crustal re-melt with minor juvenile material contribution at 2.1 Ga. These results are distinct from that for the Western Block,supporting that the Fuping Complex was emplaced in a tectonic active environment at the western margin of the Eastern Block.

  4. Changing compositions in the Iceland plume; Isotopic and elemental constraints from the Paleogene Faroe flood basalts

    DEFF Research Database (Denmark)

    Søager, Nina; Holm, Paul Martin


    -type component similar in geochemistry to the Icelandic Öræfajökull lavas. This component is believed to be recycled pelagic sediments in the plume but it can alternatively be a local crustal or lithospheric mantle component. The enriched Faroe high-Ti lavas erupted inland from the rift have isotopic......Elemental and Sr, Nd, Hf and high precision Pb isotopic data are presented from 59 low-Ti and high-Ti lavas from the syn-break up part of the Faroe Flood Basalt Province. The depleted MORB-like low-Ti lavas erupted in the rift zone between the Faroe Islands and central East Greenland around...... the time of break up of the North Atlantic have isotopic end-member compositions different from the depleted Iceland lavas. We suggest that the main low-Ti mantle component is NAEM (North Atlantic End-Member (Ellam and Stuart, 2000, J. Petrol. 41, 919) and that the 207Pb/204Pb value of the component should...

  5. Tracking the influence of a continental margin on growth of a magmatic arc, Fiordland, New Zealand, using thermobarometry, thermochronology, and zircon U-Pb and Hf isotopes (United States)

    Scott, J. M.; Cooper, A. F.; Palin, J. M.; Tulloch, A. J.; Kula, J.; Jongens, R.; Spell, T. L.; Pearson, N. J.


    Geothermobarometric, radiogenic isotopic and thermochronologic data are used to track the influence of an ancient continental margin (Western Province) on development of an adjacent Carboniferous-Cretaceous magmatic arc (Outboard Median Batholith) in Fiordland, New Zealand. The data show a record of complicated Mesozoic Gondwana margin growth. Paragneiss within the Outboard Median Batholith is of Carboniferous to Jurassic age and records burial to middle crustal depths in Late Jurassic-Early Cretaceous during subduction-related plutonism and arc thickening. In contrast, Western Province metasedimentary rocks in the area of study immediately west of the Outboard Median Batholith are Late Cambrian-Early Ordovician in age, recrystallized at the amphibolite facies in the Late Devonian-Early Carboniferous and exhibit no evidence for Mesozoic textural or isotopic reequilibration. A phase of deformation, between 128 and 116 Ma deformed, exhumed, and cooled the Outboard Median Batholith to greenschist facies temperatures, while large parts of the Western Province underwent ≥9 kbar metamorphic conditions. Zircon grains from Mesozoic inboard plutons are isotopically more evolved (ɛHf(t) = +2.3 to +4.0) than those in the Outboard Median Batholith (ɛHf(t) = +9.4 to +11.1). The contrasting zircon Hf isotope ratios, absence of S-type plutons or Proterozoic-Early Paleozoic inherited zircon, and the apparent absence of Early Paleozoic metasedimentary rocks indicates that the Outboard Median Batholith is unlikely to be underlain by the Western Province continental lithosphere. The new data are consistent with the Outboard Median Batholith representing an allochthonous (although not necessarily exotic) arc that was juxtaposed onto the Gondwana continental margin along the intervening Grebe Mylonite Zone.

  6. Zircon U-Pb Age, Trace Element, and Hf Isotope Evidence for Paleoproterozoic Granulite-Facies Metamorphism and Archean Crustal Remnant in the Dabie Orogen

    Institute of Scientific and Technical Information of China (English)

    Lei Nengzhong; Wu Yuanbao


    Zircon U-Pb age, trace elements, and Hf isotopes were determined for granulite and gneiss at Huaugtuling (黄土岭), which is hosted by ultrahigh-pressure metamorphic rocks in the Dabie(大别) orogen, east-central China. Cathodolumineseence (CL) images reveal core-rim structure for most zircons in the granulite. The cores show oscillatory zoning, relatively high Th/U and 176 Lu/177 Hf ratios, and high rare earth element (HREE)-enriched pattern, consistent with magmatic origin. They gave a weighted mean 207 Pb/206 Pb age of (2 766±9) Ma, dating magma emplacement of protolith. The rims are characterized by sector ur planar zoning, low Th/U and 176 Lu/177 Hf ratios, negative Euanomalies and flat HREE patterns, consistent with their formation under granulite-facies metamorphicconditions. Zircon U-Pb dating yields an age of (2 029±13) Ma, which is interpreted as a record ofmetamorphic event during the assembly of the supercontinent Columbia. The gneiss has a protolith ageof (1982±14) Ma, which is similar to the zircon U-Pb age for the granulite-facies metamorphism,suggesting complementary processes to granulite-facies metamorphism and partial melting. A fewinherited cores with igneous characteristics have 207 pb/206 Pb ages of approximately 3.53, 3.24, and 2.90Ga, respectively, suggesting the presence of Mesoarchean to Paleoarchean crustal remnants. A fewTriassic and Cretaceous metamorphic ages were obtained, suggesting the influences by the Triassiccontinental collision and postcollisional collapse in response to the Cretaceous extension. Comparingwith abundant occurrence of Triassic metamorphic zircons in ultrahigh-pressure eclogite and granitehydrous melt is evident for zircon growth in theHuangtuling granulite and gneiss during thecontinental collision. The magmatic protolithzircons from the granulite show a large variationin 176 Hf/177 Hf ratios from 0.280 809 to 0.281 289,corresponding to era(t) values of-7.3 to 6.3 andHf model ages of 2.74 to 3.34 Ga. The 2

  7. Magmatism as a response to exhumation of the Priest River complex, northern Idaho: Constraints from zircon U-Pb geochronology and Hf isotopes (United States)

    Stevens, L. M.; Baldwin, J. A.; Crowley, J. L.; Fisher, C. M.; Vervoort, J. D.


    Zircon and monazite U-Pb geochronology and zircon Hf isotopes place constraints on the temporal and source relationships between crustal anatexis, magmatism, and exhumation of the Priest River metamorphic core complex, northern Idaho. Granitoids that intruded the migmatitic, pelitic Hauser Lake gneiss include the pluton emplacement in the Priest River complex indicates that it was primarily a response to decompression rather than a cause. The mylonitized Silver Point and undeformed Wrencoe plutons bracket the end of a rapid phase of exhumation to c. 50-48 Ma. Zircon εHf(i) values and Lu-Hf isotope evolution indicate that the Silver Point and Wrencoe plutons crystallized from homogeneous magmas sourced from Archean-Proterozoic basement orthogneisses, whereas the Spokane granite and two leucocratic units appear to have been produced by partial melting of the Hauser Lake gneiss. Comparison of the Priest River complex with other deeply exhumed northern Cordilleran complexes indicates variability in the timing and, therefore, relative influences of partial melting and magmatism on the initiation of exhumation, which must be accounted for in numerical models of metamorphic core complex formation and evolution.

  8. What controls the isotopic composition of Greenland surface snow?

    Directory of Open Access Journals (Sweden)

    H. C. Steen-Larsen


    Full Text Available Water stable isotopes in Greenland ice core data provide key paleoclimatic information, and have been compared with precipitation isotopic composition simulated by isotopically-enabled atmospheric models. However, post-deposition processes linked with snow metamorphism remain poorly documented. For this purpose, a monitoring of the isotopic composition (δ18O, δD of surface water vapor, precipitation and samples of top (0.5 cm snow surface has been conducted during two summers (2011–2012 at NEEM, NW Greenland. The measurements also include a subset of 17O-excess measurements over 4 days, and the measurements span the 2012 Greenland heat wave. Our observations are consistent with calculations assuming isotopic equilibrium between surface snow and water vapor. We observe a strong correlation between surface vapor δ18O and air temperature (0.85 ± 0.11 ‰ °C−1 (R = 0.76 for 2012. The correlation with air temperature is not observed in precipitation data or surface snow data. Deuterium excess (d-excess is strongly anti-correlated with δ18O with a stronger slope for vapor than for precipitation and snow surface data. During nine 1–5 days periods between precipitation events, our data demonstrate parallel changes of δ18O and d-excess in surface snow and surface vapor. The changes in δ18O of the vapor are similar or larger than those of the snow δ18O. It is estimated that 6 to 20% of the surface snow mass is exchanged with the atmosphere using the CROCUS snow model. In our data, the sign of surface snow isotopic changes is not related to the sign or magnitude of sublimation or condensation. Comparisons with atmospheric models show that day-to-day variations in surface vapor isotopic composition are driven by synoptic weather and changes in air mass trajectories and distillation histories. We suggest that, in-between precipitation events, changes in the surface snow isotopic composition are driven by these changes in surface vapor isotopic

  9. What controls the isotopic composition of Greenland surface snow?

    Directory of Open Access Journals (Sweden)

    H. C. Steen-Larsen


    Full Text Available Water stable isotopes in Greenland ice core data provide key paleoclimatic information, and have been compared with precipitation isotopic composition simulated by isotopically enabled atmospheric models. However, post-depositional processes linked with snow metamorphism remain poorly documented. For this purpose, monitoring of the isotopic composition (δ18O, δD of near-surface water vapor, precipitation and samples of the top (0.5 cm snow surface has been conducted during two summers (2011–2012 at NEEM, NW Greenland. The samples also include a subset of 17O-excess measurements over 4 days, and the measurements span the 2012 Greenland heat wave. Our observations are consistent with calculations assuming isotopic equilibrium between surface snow and water vapor. We observe a strong correlation between near-surface vapor δ18O and air temperature (0.85 ± 0.11‰ °C−1 (R = 0.76 for 2012. The correlation with air temperature is not observed in precipitation data or surface snow data. Deuterium excess (d-excess is strongly anti-correlated with δ18O with a stronger slope for vapor than for precipitation and snow surface data. During nine 1–5-day periods between precipitation events, our data demonstrate parallel changes of δ18O and d-excess in surface snow and near-surface vapor. The changes in δ18O of the vapor are similar or larger than those of the snow δ18O. It is estimated using the CROCUS snow model that 6 to 20% of the surface snow mass is exchanged with the atmosphere. In our data, the sign of surface snow isotopic changes is not related to the sign or magnitude of sublimation or deposition. Comparisons with atmospheric models show that day-to-day variations in near-surface vapor isotopic composition are driven by synoptic variations and changes in air mass trajectories and distillation histories. We suggest that, in between precipitation events, changes in the surface snow isotopic composition are driven by these changes in near

  10. What controls the isotopic composition of Greenland surface snow? (United States)

    Steen-Larsen, H. C.; Masson-Delmotte, V.; Hirabayashi, M.; Winkler, R.; Satow, K.; Prié, F.; Bayou, N.; Brun, E.; Cuffey, K. M.; Dahl-Jensen, D.; Dumont, M.; Guillevic, M.; Kipfstuhl, S.; Landais, A.; Popp, T.; Risi, C.; Steffen, K.; Stenni, B.; Sveinbjörnsdottír, A. E.


    Water stable isotopes in Greenland ice core data provide key paleoclimatic information, and have been compared with precipitation isotopic composition simulated by isotopically enabled atmospheric models. However, post-depositional processes linked with snow metamorphism remain poorly documented. For this purpose, monitoring of the isotopic composition (δ18O, δD) of near-surface water vapor, precipitation and samples of the top (0.5 cm) snow surface has been conducted during two summers (2011-2012) at NEEM, NW Greenland. The samples also include a subset of 17O-excess measurements over 4 days, and the measurements span the 2012 Greenland heat wave. Our observations are consistent with calculations assuming isotopic equilibrium between surface snow and water vapor. We observe a strong correlation between near-surface vapor δ18O and air temperature (0.85 ± 0.11‰ °C-1 (R = 0.76) for 2012). The correlation with air temperature is not observed in precipitation data or surface snow data. Deuterium excess (d-excess) is strongly anti-correlated with δ18O with a stronger slope for vapor than for precipitation and snow surface data. During nine 1-5-day periods between precipitation events, our data demonstrate parallel changes of δ18O and d-excess in surface snow and near-surface vapor. The changes in δ18O of the vapor are similar or larger than those of the snow δ18O. It is estimated using the CROCUS snow model that 6 to 20% of the surface snow mass is exchanged with the atmosphere. In our data, the sign of surface snow isotopic changes is not related to the sign or magnitude of sublimation or deposition. Comparisons with atmospheric models show that day-to-day variations in near-surface vapor isotopic composition are driven by synoptic variations and changes in air mass trajectories and distillation histories. We suggest that, in between precipitation events, changes in the surface snow isotopic composition are driven by these changes in near-surface vapor

  11. Isothermal gas chromatography of short-lived Hf isotopes and element 104 in chlorinating, oxygen containing carrier gas

    Energy Technology Data Exchange (ETDEWEB)

    Jost, D.T.; Dressler, R.; Eichler, B.; Piguet, D.; Tuerler, A.; Gaeggeler, H.W.; Gaertner, M. [Paul Scherrer Inst. (PSI), Villigen (Switzerland); Grantz, M.; Huebener, S. [FZR (Germany); Buklanov, G.; Lebedev, V.; Timkhin, S.; Vedeneev, M.V.; Yakushev, A.; Zvara, I. [Joint Inst. for Nuclear Research, Dubna (Russian Federation)


    Based on thermodynamic state functions retention times of Hf and element 104 were calculated in the case of the simple adsorption of the tetrachlorides and the case of a complex adsorption involving a substitution process with oxygen in the chlorinating gas. Preliminary results for {sup 261}104 and Hf are shown. (author) 1 fig., 1 tab., 3 refs.

  12. Temporal-spatial distribution and tectonic implications of the batholiths in the Gaoligong-Tengliang-Yingjiang area, western Yunnan: Constraints from zircon U-Pb ages and Hf isotopes (United States)

    Xu, Yi-Gang; Yang, Qi-Jun; Lan, Jiang-Bo; Luo, Zhen-Yu; Huang, Xiao-Long; Shi, Yu-Ruo; Xie, Lie-Wen


    Considerable progress has recently been made regarding temporal and spatial distribution of magmatism in the Lhasa Terrane. However the eastward and southeastward correlation of these Tibetan magmatic suites in western Yunnan and Burma remains poorly constrained. This paper reports zircon U-Pb dating and Hf isotopic compositions of granites in the Gaoligong-Tengliang-Yingjiang area, west Yunnan. It reveals three episodes of plutonism, and more importantly a southwestward magmatic migration. The Gaoligong batholiths in the northeast were mainly emplaced during early Cretaceous (126-121 Ma) and comprised predominantly S-type granites with negative zircon ɛHf values (ɛHf = -2˜-12). The Tengliang granites, situated southwest of the Gaoligong belt, were emplaced in late Cretaceous (68-76 Ma) and also displayed a strong peraluminous affinity and negative ɛHf (-5˜-14), indicating a provenance from a Proterozoic sedimentary source with little mantle contribution. The youngest phase of magmatism (52-66 Ma) occurred in Yingjiang, southwestmost of the study area. It is composed of S-type granites (ɛHf = -2˜-12) in east Yingjiang and I-type granites (ɛHf = -4˜+6) in west Yingjiang, near the China-Burma border. The late Cretaceous-early Cenozoic plutons in the Tengliang and Yingjiang area are thus considered as the northern continuation of the late Cretaceous magmatic arc (west), which comprises I-type granites and andesitic rocks, and of the belt of predominant S-type granites (east) in Burma, Thailand and Malaysia. Such a chemical polarity of the dual I-type and S-type granites is strongly reminiscent of the northern American Cordillera, indicating a Cordilleran-style continental margin during the late Cretaceous-early Cenozoic. While the magmatic arc was related to eastward subduction of the Neo-Tethys beneath the Asian continent, the S-type granites represented the melting products of thickened crust in the hinterland, in response to subduction-induced decrease in

  13. Oxygen Isotope Composition of Nitrate Produced by Freshwater Nitrification (United States)

    Boshers, D.; Granger, J.; Bohlke, J. K.


    Measurements of the naturally occurring nitrogen and oxygen stable isotope ratios of nitrate (NO3-), δ15N and δ18O, can be used to determine the source, dispersal, and fate of natural and contaminant NO3- in aquatic environments. To this end, it is necessary to know the extent to which NO3- isotopologues are modified by biological reactions, as heavy and light isotopes have different reaction rates. The purpose of this study was to determine the influence of the δ18O of ambient water on the isotope composition of NO3- produced during nitrification, the biological oxidation of ammonium (NH4+) to nitrite (NO2-) and then NO3-, which is poorly constrained in freshwater systems. To determine the δ18O of NO3- produced by nitrification in freshwater, we collected water from a stream in New England, which we amended with NH4+ and with increments of 18O-enriched water, to monitor the isotope composition of NO3- produced by a natural consortium of nitrifiers. Added NH4+ was completely oxidized to NO3- over 26 days. The final δ18O of nitrified NO3- revealed sensitivity to the δ18O of water mediated by (a) isotopic equilibration between water and NO2- and (b) kinetic isotope fractionation during O-atom incorporation from water into NO2- and NO3-. Our results concur with nitrifying culture experiments that have demonstrated analogous sensitivity of the δ18O of nitrified NO3- to equilibrium and kinetic O isotope effects (Buchwald et al. 2012), as well as show that these dynamics need to be considered to interpret NO3- isotope distribution in freshwater environments.

  14. Measurement of Plutonium Isotopic Composition - MGA

    Energy Technology Data Exchange (ETDEWEB)

    Vo, Duc Ta [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)


    In this module, we will use the Canberra InSpector-2000 Multichannel Analyzer with a high-purity germanium detector (HPGe) and the MGA isotopic anlysis software to assay a variety of plutonium samples. The module provides an understanding of the MGA method, its attributes and limitations. You will assess the system performance by measuring a range of materials similar to those you may assay in your work. During the final verification exercise, the results from MGA will be combined with the 240Pueff results from neutron coincidence or multiplicity counters so that measurements of the plutonium mass can be compared with the operator-declared (certified) values.

  15. Geochemistry, zircon U-Pb dating and Hf isotopies composition of Paleozoic granitoids in Jinchuan, NW China: Constraints on their petrogenesis, source characteristics and tectonic implication (United States)

    Zeng, Renyu; Lai, Jianqing; Mao, Xiancheng; Li, Bin; Ju, Peijiao; Tao, Shilong


    Granitoids are widely distributed in Jinchuan at the southwestern margin of the North China plate, which is also an important area of mineral deposits. The research subject of this article are two Paleozoic granitoids, a cataclastic syenogranite and a granodiorite porphyry. This study presents whole rock geochemistry and zircon U-Pb-Hf isotope data for the two granitoids to determine their petrogenesis, source characteristics and tectonic significance. The cataclastic syenogranite is characterized by metaluminous composition with high potassium, and LaN/YbN from 39 to 48. The composition with strong negative Eu anomalies and Zircon saturation temperatures (TZr) from 947 to 1072 °C classify this intrusion as an A-type granite. The granodiorite porphyry is metaluminous with high sodium, sub-alkaline, LaN/YbN ratios from 27 to 32. These I-type intrusions have no Eu anomalies and TZr ranges from 818 to 845 °C. Both the cataclastic syenogranite and granodiorite porphyry show enrichment of LREE and LILE and depletion of HREE and HFSE, except Hf and Zr. Using single zircon LA-ICP-MS U-Pb dating, the emplacement age of the cataclastic syenogranite and granodiorite porphyry are determined at 433.4 ± 3.7 Ma and 361.7 ± 4.6 Ma, respectively. Zircons from the cataclastic syenogranits have uniform negative εHf(t) values (-11 ± 0.5 to -9 ± 0.5), implying the involvement of an old Palaeoproterozoic crustal source in magma genesis. The zircons from the granodiorite porphyry have εHf(t) values that range from -8 ± 1.0 to +10 ± 0.6, suggesting heterogeneous source materials involving both juvenile and ancient crust reworked crustal components. Based on the geological significance of granites at the southwestern margin of the North China plate, the closure of the North Qilian Ocean occurred at ∼444 Ma. Geochemical features suggest that the cataclastic syenogranite and granodiorite porphyry formed in an intraplate extensional and compressional setting, respectively. Hence

  16. Authentication of bell peppers using boron and strontium isotope compositions (United States)

    Rosner, Martin; Pritzkow, Wolfgang; Vogl, Jochen; Voerkelius, Susanne


    The wrong declaration of food in terms of geographical origin and production method is a major problem for the individual consumer and public regulatory authorities. The authentication of food matrices using H-C-N-O-S isotopic compositions is already well established. However, specific questions require additional isotopic systems, which are more diagonstic for the source reservoires involved or production methods used. Here we present B and Sr isotopic compositions of bell peppers from Europe (Germany, Austria, Netherlands, Spain) and Israel to verfiy their origin. The bell peppers' B isotopic compositions between different locations are highly variable (d11BNISTSRM951 -8 to +35 ‰), whereas the 87Sr/86Sr ratios are all close to modern seawater Sr isotopic composition of about 0.7092 (0.7078 to 0.7107), but still can reliably be distinguished. Distinct isotopically heavy and light B isotopic fingerprints are obtained for bell peppers from Israel and the Netherlands. Samples from Germany, Austria, and Spain display overlapping d11B values between 0 and +12 ‰. Bell peppers from Israel show high d11B values (+28 to +35 ‰) combined with 87Sr/86Sr ratios slightly more unradiogenic than modern seawater (ca 0.7079). Bell peppers from the Netherlands, however, show low d11B values (-8 ‰) combinded with 87Sr/86Sr ratios of modern seawater (approx. 0.7085). Mainly based on diagnostic B isotopic compositions bell peppers from Israel and the Netherlands can be related to a specific geographical growing environment (Israel) or production method (Netherlands). The isotope fingerprints of bell peppers from the Netherlands are consistent with growing conditions in greenhouses typical for the Netherlands vegetable farming. Using optimized production methods crops in greenhouses were supplied with nutritients by liquid fertilizers on artificial substrates. As most fertilizers derive from non-marine salt deposits, fertilization typically imprints invariant d11B values close

  17. Detrital zircon U-Pb age and Hf isotopic composition, and detrital apatite (U-Th)/He age from the Paleogene sediments of Changsha-Gongma Basin, the Songpan-Ganzi block and their geological significance%松潘甘孜长沙贡玛盆地古近纪地层碎屑锆石U-Pb年龄与Hf同位素组成及碎屑磷灰石(U-Th)/He年龄的地质意义

    Institute of Scientific and Technical Information of China (English)

    戴紧根; 李亚林; 葛玉魁


    The surface uplift and erosion of Tibetan Plateau is critical for many Cenozoic geological events ranging from continental lithosphere deformation to global cooling. Previous studies of this topic are mostly focused on Lhasa and Qiangtang blocks, central Tibetan Plateau. However, the Songpan-Ganzi block has received much less attention, resulting in the elusive understanding of its uplift history. Here we report results from sedimentology, detrital zircon U-Pb ages and Hf isotopic compositions, and detrital apatite (U-Th)/He ages from the Paleogene sediments of Changsha-Gongma Basin, western-central Songpan-Ganzi block. Sediments in the Changsha-Gongma Basin are characterized by poorly sorted conglomerate, lithic sandstone, and massive mudstone, indicating they were fast accumulations and closed to provenance area. Sample SD02 possesses four significant peak zircon ages at 200 ~500Ma, 760 ~ 1040Ma, 1800 ~2000Ma, and 2300 ~2600Ma, which are comparable with those of Triassic sandstones in the Songpan-Ganzi block, suggesting that they were all derived from the the Songpan-Ganzi block. The Songpan-Ganzi underwent one period of uplift and erosion during Late Cretaceous-Early Paleogene on the basis of the onset of Changsha-Gongma Basin sedimentation. This stage of uplift was coeval with those of central Tibetan Plateau, strongly implying that the proto-Tibetan Plateau also involved the Songpan-Ganzi block. Apatite (U-Th)/He ages from sample SD02 indicate that the Changsha-Gongma Basin experienced another stage of uplift and erosion during Late Oligocene and Early Miocene, as well as most of the Songpan-Ganzi block. Detrital zircon Hf model ages from sample SD02 are clustered at 0. 77~2. 5Ga, suggesting that the crustal growth of their preliminary provenance area largely occurred during Proterozoic.%青藏高原隆升和剥蚀是从大陆岩石圈变形到全球变冷等新生代众多地质事件诱发的关键因素.目前针对这一问题的研究主要集中在高

  18. Isotope composition and volume of Earth's early oceans. (United States)

    Pope, Emily C; Bird, Dennis K; Rosing, Minik T


    Oxygen and hydrogen isotope compositions of Earth's seawater are controlled by volatile fluxes among mantle, lithospheric (oceanic and continental crust), and atmospheric reservoirs. Throughout geologic time the oxygen mass budget was likely conserved within these Earth system reservoirs, but hydrogen's was not, as it can escape to space. Isotopic properties of serpentine from the approximately 3.8 Ga Isua Supracrustal Belt in West Greenland are used to characterize hydrogen and oxygen isotope compositions of ancient seawater. Archaean oceans were depleted in deuterium [expressed as δD relative to Vienna standard mean ocean water (VSMOW)] by at most 25 ± 5‰, but oxygen isotope ratios were comparable to modern oceans. Mass balance of the global hydrogen budget constrains the contribution of continental growth and planetary hydrogen loss to the secular evolution of hydrogen isotope ratios in Earth's oceans. Our calculations predict that the oceans of early Earth were up to 26% more voluminous, and atmospheric CH(4) and CO(2) concentrations determined from limits on hydrogen escape to space are consistent with clement conditions on Archaean Earth.

  19. Los esquistos neoproterozoicos de Santa Helena, Provincia de La Pampa, Argentina: edades u-pb shrimp, composición isotópica de hafnio e implicancias geodinámicas The Neoproterozoic Santa Elena Schists, La Pampa Province, Argentina: SHRIMP U-Pb ages, Hf isotope composition and geodynamic implications

    Directory of Open Access Journals (Sweden)

    Eduardo O Zappetini


    Full Text Available Los Esquistos Santa Helena comprenden esquistos biotítico-granatíferos predominantes y lentes gneisoides subordinadas sillimanítico- granatíferos, subaflorantes en la Estancia Santa Helena, que alcanzaron el grado metamórfico de facies anfibolita alta a granulita baja. Los circones detríticos de los esquistos datados por el método U-Pb SHRIMP son en su mayoría mesoproterozoicos y neoproterozoicos, habiendo también escasos granos paleoproterozoicos. La casi totalidad de los circones mesoproterozoicos y neoproterozoicos son de origen magmático y cristalizaron en una fuente magmática juvenil (εHf positivo, presentando edades modelo TDM de Hf entre 1127 y 1625 Ma, y entre 948 y 1274 Ma, respectivamente. Los circones paleoproterozoicos son de origen magmático y tienen una edad modelo TDM de Hf de 2310 Ma. La edad del circón detrítico más joven de los esquistos es 556 Ma, lo cual corresponde a la edad máxima de depositación, indicando que la sedimentación se habría iniciado hacia el Neoproterozoico. La completa ausencia de circones metamórficos de edad pampeana sugiere que durante la época de depositación de los Esquistos Santa Helena el núcleo metamórfico del orógeno pampeano aún no estaba constituido y expuesto. Esto contrasta con los patrones de proveniencia de los Esquistos Green, donde los circones metamórficos cámbricos son predominantes, indicando que durante su época de sedimentación (ca. 500 Ma a ca. 465 Ma el orógeno pampeano ya estaba exhumado y sujeto a denudación. Se interpreta que los Esquistos Santa Helena pertenecerían a una secuencia supracortical depositada entre los 556 y ca. 530-520 Ma en el margen sudoccidental de Gondwana en una cuenca de antepaís equivalente a la etapa tardía de la cuenca Puncoviscana. Se interpreta también que el principal aporte de los sedimentos habría provenido de la denudación de un arco magmático mesoproterozoico localizado hacia el este de los esquistos. Este arco

  20. Effects of Ti, Al and Hf on niobium silcides formation in the Nb-Si in situ composites

    Institute of Scientific and Technical Information of China (English)


    The effects of alloying elements Ti, Al and Hf on niobium silicides formation in the Nb-Si in situ composites have been investigated by scanning electron microscopy (SEM), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The binary, ternary and multicomponent alloys have been fabricated by vacuum non-consumable arc melting method. The results show that Ti tends to stabilize Nb3Si phase, while Al promotes the direct formation of β-Nb5Si3 phase with a tetrahedral D8m structure. Exceptionally, it seems that Hf is beneficial to the formation of γ-Nb5Si3 phase with a hexangular D88 structure. For the multicomponent Nb-Si in situ composites, the cooperative effects of different elements on niobium silicides formation basically maintain the character of ternary system.

  1. Complexity of In-situ zircon U-Pb-Hf isotope systematics during arc magma genesis at the roots of a Cretaceous arc, Fiordland, New Zealand (United States)

    Milan, L. A.; Daczko, N. R.; Clarke, G. L.; Allibone, A. H.


    Zircons from seventeen samples of Western Fiordland Orthogneiss (WFO) diorites and three samples of country rock (two schists and one Darran Suite diorite) from the lowermost exposed sections of the Median Batholith, Fiordland, New Zealand, were analysed for in-situ U-Pb and Hf-isotopes. The WFO represents the deeper levels of Early Cretaceous continental arc magmatism on the Pacific margin of Gondwana, marking the final stage of long-lived arc magmatism on the margin spanning the Palaeozoic. The WFO plutons were emplaced at high-P (mid to deep crust at c. 8-12 kbar) between 124 and 114 Ma. Minor very high-P (c. 18 kbar) WFO eclogite and omphacite granulite facies orthogneiss (Breaksea Orthogneiss) are inferred to have crystallised in the base of thickened crust at c. 124 Ma. Zircons from the Breaksea Orthogneiss are considered to be variably affected by Pb-loss due to emplacement of the adjacent (Malaspina) Pluton at c. 114 Ma. By identifying Pb-loss, magmatic ages were able to be inferred in respect to apparent Pb-loss ages. Hf isotope data for the WFO define an excursion to less radiogenic Hf isotope ratios with time, reflecting increased recycling of an old source component. Peaks at c. 555, 770 and 2480 Ma, determine the age spectra of inherited populations of zircons within the WFO. This contrasts with detrital zircon patterns in country rocks of the Takaka terrane, which include peaks at c. 465 Ma, and 1250-900 Ma that are absent in the WFO inheritance pattern. These results indicate a previously unrecognised Precambrian lower crustal component of New Zealand. Recycling of this lower crust became increasingly important as a source for the final stage or Mesozoic arc magmatism along this segment of the palaeo-Pacific margin of Gondwana.

  2. Tracing anthropogenic thallium in soil using stable isotope compositions. (United States)

    Kersten, Michael; Xiao, Tangfu; Kreissig, Katharina; Brett, Alex; Coles, Barry J; Rehkämper, Mark


    Thallium stable isotope data are used in this study, for the first time, to apportion Tl contamination in soils. In the late 1970s, a cement plant near Lengerich, Germany, emitted cement kiln dust (CKD) with high Tl contents, due to cocombustion of Tl-enriched pyrite roasting waste. Locally contaminated soil profiles were obtained down to 1 m depth and the samples are in accord with a binary mixing relationship in a diagram of Tl isotope compositions (expressed as ε(205)Tl, the deviation of the (205)Tl/(203)Tl ratio of a sample from the NIST SRM 997 Tl isotope standard in parts per 10(4)) versus 1/[Tl]. The inferred mixing endmembers are the geogenic background, as defined by isotopically light soils at depth (ε(205)Tl ≈ -4), and the Tl emissions, which produce Tl-enriched topsoils with ε(205)Tl as high as ±0. The latter interpretation is supported by analyses of the CKD, which is also characterized by ε(205)Tl ≈ ± 0, and the same ε(205)Tl value was found for a pyrite from the deposit that produced the cocombusted pyrite roasting waste. Additional measurements for samples from a locality in China, with outcrops of Tl sulfide mineralization and associated high natural Tl backgrounds, reveal significant isotope fractionation between soils (ε(205)Tl ≈ +0.4) and locally grown green cabbage (ε(205)Tl between -2.5 and -5.4). This demonstrates that biological isotope fractionation cannot explain the isotopically heavy Tl in the Lengerich topsoils and the latter are therefore clearly due to anthropogenic Tl emissions from cement processing. Our results thus establish that isotopic data can reinforce receptor modeling for the toxic trace metal Tl.

  3. Petrogenesis of Late Mesozoic granitoids and coeval mafic rocks from the Jiurui district in the Middle-Lower Yangtze metallogenic belt of Eastern China: Geochemical and Sr-Nd-Pb-Hf isotopic evidence (United States)

    Xu, Yao-Ming; Jiang, Shao-Yong; Zhu, Zhi-Yong; Yang, Shui-Yuan; Zhou, Wei


    Large-scale Cu-Au mineralization is associated with the Late Mesozoic granitoids in the Jiurui district of the Middle-Lower Yangtze Mineralization Belt in Eastern China. To constrain the petrogenesis of these granitoids and coeval mafic rocks, a detailed geochemical and Sr-Nd-Pb-Hf isotopic study was performed. The Jiurui granitoids are made up primarily of granodiorite porphyry and quartz diorite porphyry. These granitoids are characterized by SiO2 and K2O contents of 58.8 wt.% to 68.6 wt.% and 1.9 wt.% to 5.7 wt.%, respectively. These granitoids show relatively high MgO contents (1.0 wt.% to 3.1 wt.%, average 2.1 wt.%) and high Mg# values (39 to 70, average 54). The Jiurui granitoids are enriched in light rare earth elements (LREE), large ion lithophile elements (LILE), and compatible trace elements (Cr, Ni and V) but are relatively depleted in Nb, Ta, Y and Yb. These rocks show a negligible negative Eu anomaly (Eu/Eu* = 0.76-1.13, average 0.91) and nearly no negative Sr anomaly. The whole-rock initial 87Sr/86Sr ratios range from 0.7060 to 0.7092, and the ɛNd(t) values vary from - 5.4 to - 2.0. The granitoids show radiogenic Pb isotopic ratios with values of 206Pb/204Pb (17.93-18.21), 207Pb/204Pb (15.55-15.58), and 208Pb/204Pb (38.16-38.56) for the plagioclases. The zircon Hf isotopic compositions show ɛHf(t) values from - 11.8 to 2.4. The coeval mafic rocks consist of lamprophyre, diabase and fine-grained mafic dyke. These rocks are characterized by SiO2 contents ranging from 47.6 wt.% to 54.8 wt.%, with a negative Eu anomaly and a positive to negative Sr anomaly. The whole-rock initial 87Sr/86Sr ratios range from 0.7059 to 0.7071, and the ɛNd(t) values vary from - 3.8 to - 1.4. By comparing the geochemical and isotopic compositions of the Jiurui granitoids and the coeval mafic rocks, we conclude that the granitoids are similar to adakites that were likely related to the delamination processes, and the coeval mafic rocks may have originated directly from

  4. Characteristics of carbon and hydrogen isotopic compositions of light hydrocarbons

    Institute of Scientific and Technical Information of China (English)



    Light hydrocarbons named in the present paper refer to the natural gas-associated light oil and condensate 46 light oil and condensate samples from 11 oil-bearing basins of China were collected and their carbon and hydrogen isotopic compositions were analysed in terms of their total hydrocarbons, saturated hydrocarbons and a part of aromatic fractions, and gas-source materials and their sedimentary environments were discussed based on the above-mentioned data and the geological background of each area. From the view of carbon and hydrogen isotopic composition of total hydrocarbons and saturated hydrocarbons, it is revealed that the condensate related to coal-bearing strata is enriched in 13C and D while that related to the source material of type I-II is enriched in 12C. In general, the isotopic composition of carbon is mainly attributed to the inheriting effect of their source materials, whereas that of hydrogen principally reflects the correlationship between hydrogen isotopes and the sedimentary envi

  5. The isotopic composition of solar flare accelerated neon (United States)

    Mewaldt, R. A.; Spalding, J. D.; Stone, E. C.; Vogt, R. E.


    The individual isotopes of neon in energetic solar-flare particles have been clearly resolved with a rms mass resolution of 0.20 amu. The ratios found are Ne-20/Ne-22 = 7.6 (+2.0, -1.8) and Ne-21/Ne-22 of no more than about 0.11 in the 11-26 MeV per nucleon interval. This isotopic composition is essentially the same as that of meteoritic planetary neon-A and is significantly different from that of the solar wind.

  6. Stable isotope composition and volume of Early Archaean oceans

    DEFF Research Database (Denmark)

    Pope, Emily Catherine; Rosing, Minik Thorleif; Bird, Dennis K.

    Oxygen and hydrogen isotope compositions of seawater are controlled by volatile fluxes between mantle, lithospheric (oceanic and continental crust) and atmospheric reservoirs. Throughout geologic time oxygen was likely conserved within these Earth system reservoirs, but hydrogen was not, as it can...... escape to space [1]. Hydrogen isotope ratios of serpentinites from the ~3.8Ga Isua Supracrustal Belt in West Greenland are between -53 and -99‰; the highest values are in antigorite ± lizardite serpentinites from a low-strain lithologic domain where hydrothermal reaction of Archaean seawater with oceanic...

  7. Do foraminifera accurately record seawater neodymium isotope composition? (United States)

    Scrivner, Adam; Skinner, Luke; Vance, Derek


    Palaeoclimate studies involving the reconstruction of past Atlantic meridional overturning circulation increasingly employ isotopes of neodymium (Nd), measured on a variety of sample media (Frank, 2002). In the open ocean, Nd isotopes are a conservative tracer of water mass mixing and are unaffected by biological and low-temperature fractionation processes (Piepgras and Wasserburg, 1987; Lacan and Jeandel, 2005). For decades, benthic foraminifera have been widely utilised in stable isotope and geochemical studies, but have only recently begun to be exploited as a widely distributed, high-resolution Nd isotope archive (Klevenz et al., 2008), potentially circumventing the difficulties associated with other methods used to recover past deep-water Nd isotopes (Klevenz et al., 2008; Rutberg et al., 2000; Tachikawa et al., 2004). Thus far, a single pilot study (Klevenz et al., 2008) has indicated that core-top sedimentary benthic foraminifera record a Nd isotope composition in agreement with the nearest available bottom seawater data, and has suggested that this archive is potentially useful on both millennial and million-year timescales. Here we present seawater and proximal core-top foraminifer Nd isotope data for samples recovered during the 2008 "RETRO" cruise of the Marion Dufresne. The foraminifer samples comprise a depth-transect spanning 3000m of the water column in the Angola Basin and permit a direct comparison between high-resolution water column and core-top foraminiferal Nd isotope data. We use these data to assess the reliability of both planktonic and benthic foraminifera as recorders of water column neodymium isotope composition. Frank, M., 2002. Radiogenic isotopes: Tracers of past ocean circulation and erosional input, Rev. Geophys., 40 (1), 1001, doi:10.1029/2000RG000094. Klevenz, V., Vance, D., Schmidt, D.N., and Mezger, K., 2008. Neodymium isotopes in benthic foraminifera: Core-top systematics and a down-core record from the Neogene south Atlantic

  8. C-isotope composition of fossil sedges and grasses (United States)

    Kurschner, Wolfram M.


    C4 plants differ from C3 plants regarding their anatomy and their C-isotope composition. Both features can be used in the geological record to determine the presence of C4 plants. Yet, the evolution of the C4 pathway in the fossil record is enigmatic as palaeobotanical and geological evidence for C4 plants is sparse. The oldest structural evidence for Kranz anatomy has been found in Late Miocene permineralized grass leaf remains. But studies on the C-isotope composition of sedimentary organic matter indicate that abundant C4 biomass was present in N-America and Asia throughout the Miocene in expanding savannahs and grasslands. The success of C4 plants appears to be related also to an increasing seasonal aridity in the tropical climate belts and the co-evolution of grazers. However, C- isotope composition of palaeosols or vertebrate teeth only allows to estimate the abundance of C4 plant biomass in the vegetation or in the diet without further taxonomical specification which plant groups would have had C4 metabolism. In this contribution the first extensive C-isotope analysis of fossil seeds of sedges and a few grasses are presented. The age of the carpological material ranges from Late Eocene to Pliocene and was collected from several central European brown coal deposits. The 52 different taxa studied include several species of Carex, Cladiocarya, Eriopherum, Eleocharis, Scirpus, Sparganium. Most of them representing herbaceous elements of a (sub)tropical vegetation growing near the edge of a lake. The C-isotope composition of the fossil seeds varies between -30 and -23 o/oo indicating C3 photosynthesis. This first systematic inventory shows that C4 plants were absent in the European (sub)tropical brown coal forming wetland vegetation during the Tertiary. These preliminary data are in agreement with phylogenetic studies which predict the origin of C4 plants outside the European realm.

  9. Boron isotopic compositions of some boron minerals

    Energy Technology Data Exchange (ETDEWEB)

    Oi, Takao; Musashi, Masaaki; Ossaka, Tomoko; Kakihana, Hidetake (Sophia Univ., Tokyo (Japan)); Nomura, Masao; Okamoto, Makoto (Tokyo Institute of Technology (Japan))


    Boron minerals that have different structural formulae but are supposed to have the same geologic origin have been collected and analyzed for the {sup 11}B/{sup 10}B isotopic ratio. It has been reconfirmed that minerals of marine origin have higher {sup 11}B/{sup 10}B ratios than those of nonmarine origin. It has been found that the sequence of decreasing {sup 11}B/{sup 10}B values among the minerals with the same geologic origin is; borax, tincal, kernite (Na borates) > ulexite (Na/Ca borate) > colemanite, iyoite, meyerhofferite (Ca borates). This sequence is explainable on the basis of the difference in crystal structure among the minerals. That is, minerals with high BO{sub 3}/BO{sub 4} ratios, (the ratio of the number of the BO{sub 3} triangle units to the number of the BO{sub 4} tetrahedron units in the structural formula of a mineral) have higher {sup 11}B/{sup 10}B ratios.

  10. Stable isotope composition and volume of Early Archaean oceans

    DEFF Research Database (Denmark)

    Pope, Emily Catherine; Rosing, Minik Thorleif; Bird, Dennis K.

    Oxygen and hydrogen isotope compositions of seawater are controlled by volatile fluxes between mantle, lithospheric (oceanic and continental crust) and atmospheric reservoirs. Throughout geologic time oxygen was likely conserved within these Earth system reservoirs, but hydrogen was not, as it can...... escape to space [1]. Hydrogen isotope ratios of serpentinites from the ~3.8Ga Isua Supracrustal Belt in West Greenland are between -53 and -99‰; the highest values are in antigorite ± lizardite serpentinites from a low-strain lithologic domain where hydrothermal reaction of Archaean seawater with oceanic...... of continents present at that time), and the mass of Early Archaean oceans to ~109 to 126% of present day oceans. Oxygen isotope analyses from these Isua serpentinites (δ18O = +0.1 to 5.6‰ relative to VSMOW) indicate that early Archaean δ18OSEAWATER similar to modern oceans. Our observations suggest...

  11. Triple oxygen isotope composition of the Campi Flegrei magma systems (United States)

    Iovine, Raffaella Silvia; Wörner, Gerhard; Pack, Andreas; Sengupta, Sukanya; Carmine Mazzeo, Fabio; Arienzo, Ilenia; D'Antonio, Massimo


    Sr-O isotope relationships in igneous rocks are a powerful tool to distinguish magma sources and quantify assimilation processes in magmatic rocks. Isotopic (87Sr/86Sr and 18O/16O-17O/16O) data have been acquired on whole rocks and separated minerals (feldspar, Fe-cpx, Mg-cpx, olivine phenocrysts) from pyroclastic products of the Campi Flegrei volcanic complex (Gulf of Naples, Southern Italy). Oxygen isotope ratios were measured by infrared laser fluorination using a Thermo MAT253 gas source isotope ratio mass spectrometer in dual inlet mode, on ˜2 mg of hand-picked phenocrysts. Variations in triple oxygen isotope ratios (17O/16O, 18O/16O) are expressed as the δ notation relative to VSMOW. Sr isotopic compositions were determined by thermal ionization mass spectrometry after standard cation-exchange methods on separated hand-picked phenocrysts (˜300 mg), and on whole rocks, in case of insufficient sample size to separate crystals. Sr-isotopes in Campi Flegrei minerals range from 0.707305 to 0.707605 and δ18O varies from 6.5 to 8.3‰ . Recalculated δ18Omelt values accordingly show a large range between 7.2 and 8.6‰ . Our data, compared with published δ18O-isotope data from other Italian volcanic centers (Alban Hills, Mts. Ernici, Ischia, Mt. Vesuvius, Aeolian Islands, Tuscany and Sardinia) and from subduction zones worldwide (Kamchatka, Lesser Antilles, Indonesia and Central Andean ignimbrites), show compositions that are very different from typical mantle values. Distinct trends and sources are recognized in our compilation from global data: (1) serpentinized mantle (Kamchatka), (2) sediment-enrichment in the mantle source (Indonesia, Lesser Antilles, Eolian arc), (3) assimilation of old radiogenic continental crust affecting magmas derived from sediment-modified mantle sources (Tuscany, Sardinia), (4) assimilation of lower crustal lithologies (Central Andes, Alban Hills, Mts. Ernici, Ischia). Sr-O-isotope values of Campi Flegrei and Vesuvius magmas

  12. Stable isotopic composition of bottled mineral waters from Romania (United States)

    Bădăluţă, Carmen; Nagavciuc, Viorica; Perșoiu, Aurel


    Romania has a high potential of mineral waters resources, featuring one of the largest mineral resources at European and global level. In the last decade, due to increased in consumption of bottled water, numerous brands have appeared on the market, with equally numerous and variable sources of provenance. In this study we have analyzed the isotopic composition of bottled mineral waters from Romania in order to determine their source and authenticity. We have analysed 32 carbonated and 24 non-carbonated mineral waters from Romania. and the results were analysed in comparison with stable isotope data from precipitation and river waters. Generally, the isotopic values of the mineral waters follow those in precipitation; however, differences occur in former volcanic regions (due to deep circulation of meteoric waters and increased exchange with host rock and volcanic CO2), as well as in mountainous regions, where high-altitude recharge occurs.

  13. The chromium isotope composition of reducing and oxic marine sediments (United States)

    Gueguen, Bleuenn; Reinhard, Christopher T.; Algeo, Thomas J.; Peterson, Larry C.; Nielsen, Sune G.; Wang, Xiangli; Rowe, Harry; Planavsky, Noah J.


    The chromium (Cr) isotope composition of marine sediments has the potential to provide new insights into the evolution of Earth-surface redox conditions. There are significant but poorly constrained isotope fractionations associated with oxidative subaerial weathering and riverine transport, the major source of seawater Cr, and with partial Cr reduction during burial in marine sediments, the major sink for seawater Cr. A more comprehensive understanding of these processes is needed to establish global Cr isotope mass balance and to gauge the utility of Cr isotopes as a paleoredox proxy. For these purposes, we investigated the Cr isotope composition of reducing sediments from the upwelling zone of the Peru Margin and the deep Cariaco Basin. Chromium is present in marine sediments in both detrital and authigenic phases, and to estimate the isotopic composition of the authigenic fraction, we measured δ53Cr on a weakly acid-leached fraction in addition to the bulk sediment. In an effort to examine potential variability in the Cr isotope composition of the detrital fraction, we also measured δ53Cr on a variety of oxic marine sediments that contain minimal authigenic Cr. The average δ53Cr value of the oxic sediments examined here is -0.05 ± 0.10‰ (2σ, n = 25), which is within the range of δ53Cr values characteristic of the bulk silicate Earth. This implies that uncertainty in estimates of authigenic δ53Cr values based on bulk sediment analyses is mainly linked to estimation of the ratio of Cr in detrital versus authigenic phases, rather than to the Cr-isotopic composition of the detrital pool. Leaches of Cariaco Basin sediments have an average δ53Cr value of +0.38 ± 0.10‰ (2σ, n = 7), which shows no dependency on sample location within the basin and is close to that of Atlantic deepwater Cr (∼+0.5‰). This suggests that authigenic Cr in anoxic sediments may reliably reflect the first-order Cr isotope composition of deepwaters. For Peru Margin samples

  14. Source and mode of the Permian Panjal Trap magmatism: Evidence from zircon U-Pb and Hf isotopes and trace element data from the Himalayan ultrahigh-pressure rocks (United States)

    Rehman, Hafiz Ur; Lee, Hao-Yang; Chung, Sun-Lin; Khan, Tahseenullah; O'Brien, Patrick J.; Yamamoto, Hiroshi


    We present an integrated study of LA-ICP-MS U-Pb age, Hf isotopes, and trace element geochemistry of zircons from the Himalayan eclogites (mafic rocks) and their host gneisses (felsic rocks) from the Kaghan Valley in Pakistan in order to understand the source and mode of their magmatic protoliths and the effect of metamorphism. Zircons from the so-called Group I (high-pressure) eclogites yielded U-Pb mean ages of 259 ± 10 Ma (MSWD = 0.74), whereas those of Group II (ultrahigh-pressure) eclogites yielded 48 ± 3 Ma (MSWD = 0.71). In felsic gneisses the central or core domains of zircons yielded ages similar to those from Group I eclogites but zircon overgrowth domains yielded 47 ± 1 Ma (MSWD = 1.9). Trace element data suggest a magmatic origin for Group I-derived (having Th/U ratios: > 0.5) and metamorphic origin for Group II-derived (Th/U rocks (Panjal Traps) with almost no contribution from the ancient crustal material. The similar ƐHf(t) values, identical protolith ages and trace element compositions of zircons in felsic (granites or rhyolites) and mafic (basalt and dolerite) rocks attest to a bimodal magmatism accounting for the Panjal Traps during the Permian. Later, during India-Asia collision in Eocene times, both the felsic and mafic lithologies were subducted to mantle-depths (> 90 km: coesite-stable) and experienced ultrahigh-pressure metamorphism before their final exhumation.

  15. Modeling the carbon isotope composition of bivalve shells (Invited) (United States)

    Romanek, C.


    The stable carbon isotope composition of bivalve shells is a valuable archive of paleobiological and paleoenvironmental information. Previous work has shown that the carbon isotope composition of the shell is related to the carbon isotope composition of dissolved inorganic carbon (DIC) in the ambient water in which a bivalve lives, as well as metabolic carbon derived from bivalve respiration. The contribution of metabolic carbon varies among organisms, but it is generally thought to be relatively low (e.g., organism and high (>90%) in the shells from terrestrial organisms. Because metabolic carbon contains significantly more C-12 than DIC, negative excursions from the expected environmental (DIC) signal are interpreted to reflect an increased contribution of metabolic carbon in the shell. This observation contrasts sharply with modeled carbon isotope compositions for shell layers deposited from the inner extrapallial fluid (EPF). Previous studies have shown that growth lines within the inner shell layer of bivalves are produced during periods of anaerobiosis when acidic metabolic byproducts (e.g., succinic acid) are neutralized (or buffered) by shell dissolution. This requires the pH of EPF to decrease below ambient levels (~7.5) until a state of undersaturation is achieved that promotes shell dissolution. This condition may occur when aquatic bivalves are subjected to external stressors originating from ecological (predation) or environmental (exposure to atm; low dissolved oxygen; contaminant release) pressures; normal physiological processes will restore the pH of EPF when the pressure is removed. As a consequence of this process, a temporal window should also exist in EPF at relatively low pH where shell carbonate is deposited at a reduced saturation state and precipitation rate. For example, EPF chemistry should remain slightly supersaturated with respect to aragonite given a drop of one pH unit (6.5), but under closed conditions, equilibrium carbon isotope

  16. Sr and Nd isotopic and trace element compositions of Quaternary volcanic centers of the southern Andes

    Energy Technology Data Exchange (ETDEWEB)

    Futa, Kiyoto; Stern, C.R.


    Isotopic compositions of samples from six Quaternary volcanoes located in the northern and southern extremities of the Southern Volcanic Zone (SVZ, 33-46/sup 0/S) of the Andes and from four centers in the Austral Volcanic Zone (AVZ, 49-54/sup 0/S) range for /sup 87/Sr//sup 86/Sr from 0.70280 to 0.70591 and for /sup 143/Nd//sup 144/Nd from 0.51314 to 0.51255. Basalts and basaltic andesites from three centers just north of the Chile Rise-Trench triple junction have /sup 87/Sr//sup 86/Sr, /sup 143/Nd//sup 144/Nd, La/Yb, Ba/La and Hf/Lu that lie within the relatively restricted ranges of the basic magmas erupted from the volcanic centers as far north as 35/sup 0/S in the SVZ of the Andes. The trace element and Sr and Nd isotopic characteristics of these magmas may be explained by source region contamination of subarc asthenosphere, with contaminants derived from subducted pelagic sediments and seawater-altered basalts by dehydration of subducted oceanic lithosphere. In the northern extremity of the SVZ between 33/sup 0/ and 34/sup 0/S, basaltic andesites and andesites have higher /sup 87/Sr//sup 86/Sr, Rb/Cs, and Hf/Lu, and lower /sup 143/Nd//sup 144/Nd than basalts and basaltic andesites erupted farther south in the SVZ, which suggests involvement of components derived from the continental crust. In the AVZ, the most primitive sample, high-Mg andesite from the southernmost volcanic center in the Andes (54/sup 0/S) has Sr and Nd isotopic compositions and K/Rb and Ba/La similar to MORB. The high La/Yb of this sample suggests formation by small degrees of partial melting of subducted MORB with garnet as a residue. Samples from centers farther north in the AVZ show a regionally regular northward increase in SiO/sub 2/, K/sub 2/O, Rb, Ba, Ba/La, and /sup 87/Sr//sup 86/Sr and decrease in MgO, Sr, K/Rb, Rb/Cs, and /sup 143/Nd//sup 144/Nd, suggesting increasingly greater degrees of fractional crystallization and associated intra-crustal contamination. (orig./SHOE).

  17. Early Earth differentiation processes investigated through the short-lived 146Sm-142Nd and 182Hf-182W isotope systems (United States)

    Rizo Garza, H. L.; Walker, R. J.; Carlson, R.; Touboul, M.; Horan, M. F.; Puchtel, I. S.; Boyet, M.; Rosing, M. T.


    The earliest history of Earth is difficult to capture due to the scarcity and high degrees of alteration of ancient terrains. Nevertheless, short-lived isotope systems can provide important constraints on early geological processes. The 182Hf-182W (t1/2 = 8.9 Ma) and 146Sm-142Nd (t1/2=103 Ma) systems are variably sensitive to differentiation processes that occurred during the first 50 Ma and 500 Ma of Earth's history, respectively. Eoarchean mantle-derived rocks from the Isua supracrustal belt (southwest Greenland) show well-resolved anomalies in both 182W (+5 to +21 ppm) and 142Nd (-10 to +15 ppm) compared to terrestrial standards. While there is evidence that W was mobilized in the crust accessed by the Isua suite, W and Nd isotopic anomalies are interpreted to primarily reflect Hadean processes that affected the mantle precursors of these rocks. Variations in 142Nd do not correlate with those of 182W, however, suggesting different mechanisms for the origin and retention of the isotopic anomalies present in these two systems. The 142Nd data, combined with 143Nd data for the long-lived 147Sm-143Nd system, are interpreted to reflect silicate crystal-liquid fractionation 4.3 Ga ago. Variations of 182W in the Isua lavas mantle source could also have been produced as a result of Hf/W fractionation caused by silicate differentiation during the lifetime of 182Hf, but these processes would have to somehow be decoupled from the processes that affected Sm/Nd. Alternatively, 182W variability could be the result of combined early Hf/W fractionations caused by metal-silicate segregation within discrete mantle domains and late accretion processes. Variations in 182W and 142Nd observed in the Isua supracrustal rocks are similar to those observed in the ancient rocks from Nuvvuagittuq Greenstone Belt, the Acasta Gneiss Complex, and the Saglek Block, suggesting that similar processes affected diverse early Earth rocks.

  18. Phase and Microstructural Correlation of Spark Plasma Sintered HfB2-ZrB2 Based Ultra-High Temperature Ceramic Composites

    Directory of Open Access Journals (Sweden)

    Ambreen Nisar


    Full Text Available The refractory diborides (HfB2 and ZrB2 are considered as promising ultra-high temperature ceramic (UHTCs where low damage tolerance limits their application for the thermal protection system in re-entry vehicles. In this regard, SiC and CNT have been synergistically added as the sintering aids and toughening agents in the spark plasma sintered (SPS HfB2-ZrB2 system. Herein, a novel equimolar composition of HfB2 and ZrB2 has shown to form a solid-solution which then allows compositional tailoring of mechanical properties (such as hardness, elastic modulus, and fracture toughness. The hardness of the processed composite is higher than the individual phase hardness up to 1.5 times, insinuating the synergy of SiC and CNT reinforcement in HfB2-ZrB2 composites. The enhanced fracture toughness of CNT reinforced composite (up to a 196% increment surpassing that of the parent materials (ZrB2/HfB2-SiC is attributed to the synergy of solid solution formation and enhanced densification (~99.5%. In addition, the reduction in the analytically quantified interfacial residual tensile stress with SiC and CNT reinforcements contribute to the enhancement in the fracture toughness of HfB2-ZrB2-SiC-CNT composites, mandatory for aerospace applications.

  19. Similar crustal evolution in the western units of the Adrar Souttouf Massif (Moroccan Sahara) and the Avalonian terranes: Insights from Hf isotope data (United States)

    Gärtner, Andreas; Villeneuve, Michel; Linnemann, Ulf; Gerdes, Axel; Youbi, Nasrrddine; Hofmann, Mandy


    The Adrar Souttouf Massif is located at the western margin of the West African Craton and consists of several NNE-SSW trending units. Of them, the two westernmost have been interpreted to be linked with the Avalonian terrane assemblage and Meguma, respectively. New Hf isotopic data corroborates the Avalon correlation but has no impact one way or another on the possible Meguma connection, as there is no Hf data available from the latter. The obtained pattern of εHf(t) values vs. zircon age of the likely Avalonia related Oued Togba unit is similar to published data from Avalonia. Zircons of this unit show characteristic patterns of crustal mixing at 0.7 to 1.3 Ga and 1.75 to 2.25 Ga, while juvenile crust was likely formed around 0.6 to 0.75 Ga, from 1.2 to 2.2 Ga, and between 2.5 and 3.2 Ga. The zircons of the Sebkha Gezmayet unit reveal crustal mixing for the entire Palaeozoic and Neoproterozoic, from 2.05 to 2.11 Ga, and 2.8 to 2.9 Ga. Juvenile crust formation is interpreted to have occurred from 0.5 to 0.7 Ga, at around 2.1 Ga, and at ca. 2.9 Ga. As Mesoproterozoic zircons are abundant in the likely Avalonia-like Oued Togba unit, but uncommon at the West African Craton, their origin has to be found elsewhere. A comparison of available Hf data from Amazonia and Baltica, the two potential source cratons of Avalonia, shows similarities but is hampered by the lack of available data from Amazonia. Finally, a few grains from both units have Eoarchaean model ages. Among similar grains from other peri-Gondwanan terranes, they give indication of partial recycling of Eoarchaean crust in the vicinity of the northwestern West African Craton.

  20. Alkali elemental and potassium isotopic compositions of Semarkona chondrules (United States)

    Alexander, C.M. O'D.; Grossman, J.N.


    We report measurements of K isotope ratios in 28 Semarkona chondrules with a wide range of petrologic types and bulk compositions as well as the compositions of CPX-mesostasis pairs in 17 type I Semarkona chondrules, including two chondrules with radial alkali zonation and 19 type II chondrules. Despite the wide range in K/Al ratios, no systematic variations in K isotopic compositions were found. Semarkona chondrules do not record a simple history of Rayleigh-type loss of K. Experimentally determined evaporation rates suggest that considerable alkali evaporation would have occurred during chondrule formation. Nevertheless, based on Na CPX-mesostasis distribution coefficients, the alkali contents of the cores of most chondrules in Semarkona were probably established at the time of final crystallization. However, Na CPX-mesostasis distribution coefficients also show that alkali zonation in type I Semarkona chondrules was produced by entry of alkalis after solidification, probably during parent body alteration. This alkali metasomatism may have gone to completion in some chondrules. Our preferred explanation for the lack of systematic isotopic enrichments, even in alkali depleted type I chondrule cores, is that they exchanged with the ambient gas as they cooled. ?? The Meteoritical Society, 2005.

  1. Light and heavy element isotopic compositions of mainstream SiC grains.

    Energy Technology Data Exchange (ETDEWEB)

    Amari, S.; Clayton, R. N.; Davis, A. M.; Lewis, R. S.; Pellin, M. J.


    Although a variety of types of pre-solar SiC grains have been classified by their C, N, and Si isotopic composition, the majority of such grains are so-called mainstream grains and are believed to have come from asymptotic giant branch stars [1]. We have previously reported the Mo isotopic compositions of presolar SiC grains whose C, N, and Si isotopic compositions were not known [2]. Since most presolar SiC grains fall in the mainstream group, we assumed that these grains were mainstream. The excellent match of the Mo isotopic data with expectations for nucleosynthesis in AGB stars was consistent with this identification. In order to better understand the distribution of isotopic compositions in presolar grains, we have begun to measure heavy element isotopic compositions of presolar SiC grains of known C, N and Si isotopic composition.

  2. Clumped-isotope geochemistry of carbonates: A new tool for the reconstruction of temperature and oxygen isotope composition of seawater

    Energy Technology Data Exchange (ETDEWEB)

    Bernasconi, Stefano M., E-mail: [Geological Institute, ETH Zuerich, Sonneggstrasse 5, 8092 Zuerich (Switzerland); Schmid, Thomas W.; Grauel, Anna-Lena [Geological Institute, ETH Zuerich, Sonneggstrasse 5, 8092 Zuerich (Switzerland); Mutterlose, Joerg [Institut fuer Geologie, Mineralogie und Geophysik, Ruhr Universitaet Bochum, Universitaetsstr. 150, 44801 Bochum (Germany)


    Highlights: > Clumped-isotope thermometry of carbonates is discussed. > Clumped isotopes of Belemnites show higher sea surface temperatures than commonly assumed for the lower Cretaceous. > The potential of clumped-isotope measurement on foraminifera is discussed. - Abstract: Clumped-isotope geochemistry deals with State of ordering of rare isotopes in molecules, in particular with their tendency to form bonds with other rare isotopes rather than with the most abundant ones. Among its possible applications, carbonate clumped-isotope thermometry is the one that has gained most attention because of the wide potential of applications in many disciplines of the earth sciences. In particular, it allows reconstructing the temperature of formation of carbonate minerals without knowledge of the isotopic composition of the water from which they were formed. In addition, the O isotope composition of the waters from which they were formed can be calculated using the {delta}{sup 18}O of the same carbonate sample. This feature offers new approaches in paleoclimatology for reconstructing past global geochemical cycles. In this contribution two applications of this method are presented. First the potential of a new analytical method of measurement of clumped isotopes on small samples of foraminifera, for high-resolution SST and seawater {delta}{sup 18}O reconstructions from marine sediments is shown. Furthermore the potential of clumped isotope analysis of belemnites, for reconstructing seawater {delta}{sup 18}O and temperatures in the Cretaceous is shown.

  3. Magnesium stable isotope composition of Earth's upper mantle (United States)

    Handler, Monica R.; Baker, Joel A.; Schiller, Martin; Bennett, Vickie C.; Yaxley, Gregory M.


    The mantle is Earth's largest reservoir of Mg containing > 99% of Earth's Mg inventory. However, no consensus exists on the stable Mg isotope composition of the Earth's mantle or how variable it is and, in particular, whether the mantle has the same stable Mg isotope composition as chondrite meteorites. We have determined the Mg isotope composition of olivine from 22 mantle peridotites from eastern Australia, west Antarctica, Jordan, Yemen and southwest Greenland by pseudo-high-resolution MC-ICP-MS on Mg purified to > 99%. The samples include fertile lherzolites, depleted harzburgites and dunites, cryptically metasomatised ('dry') peridotites and modally metasomatised apatite ± amphibole-bearing harzburgites and wehrlites. Olivine from these samples of early Archaean through to Permian lithospheric mantle have δ25Mg DSM-3 = - 0.22 to - 0.08‰. These data indicate the bulk upper mantle as represented by peridotite olivine is homogeneous within current analytical uncertainties (external reproducibility ≤ ± 0.07‰ [2 sd]). We find no systematic δ25Mg variations with location, lithospheric age, peridotite fertility, or degree or nature of mantle metasomatism. Although pyroxene may have slightly heavier δ25Mg than coexisting olivine, any fractionation between mantle pyroxene and olivine is also within current analytical uncertainties with a mean Δ25Mg pyr-ol = +0.06 ± 0.10‰ (2 sd; n = 5). Our average mantle olivine δ25Mg DSM-3 = - 0.14 ± 0.07‰ and δ26Mg DSM-3 = - 0.27 ± 0.14‰ (2 sd) are indistinguishable from the average of data previously reported for terrestrial basalts, confirming that basalts have stable Mg isotope compositions representative of the mantle. Olivine from five pallasite meteorites have δ25Mg DSM-3 = - 0.16 to - 0.11‰ that are identical to terrestrial olivine and indistinguishable from the average δ25Mg previously reported for chondrites. These data provide no evidence for measurable heterogeneity in the stable Mg isotope

  4. The triple isotopic composition of oxygen in leaf water (United States)

    Landais, A.; Barkan, E.; Yakir, D.; Luz, B.


    The isotopic composition of atmospheric O 2 depends on the rates of oxygen cycling in photosynthesis, respiration, photochemical reactions in the stratosphere and on δ17O and δ18O of ocean and leaf water. While most of the factors affecting δ17O and δ18O of air O 2 have been studied extensively in recent years, δ17O of leaf water—the substrate for all terrestrial photosynthesis—remained unknown. In order to understand the isotopic composition of atmospheric O 2 at present and in fossil air in ice cores, we studied leaf water in field experiments in Israel and in a European survey. We measured the difference in δ17O and δ18O between stem and leaf water, which is the result of isotope enrichment during transpiration. We calculated the slopes of the lines linking the isotopic compositions of stem and leaf water. The obtained slopes in ln( δ17O + 1) vs. ln( δ18O + 1) plots are characterized by very high precision (˜0.001) despite of relatively large differences between duplicates in both δ17O and δ18O (0.02-0.05‰). This is so because the errors in δ18O and δ17O are mass-dependent. The slope of the leaf transpiration process varied between 0.5111 ± 0.0013 and 0.5204 ± 0.0005, which is considerably smaller than the slope linking liquid water and vapor at equilibrium (0.529). We further found that the slope of the transpiration process decreases with atmospheric relative humidity ( h) as 0.522-0.008 × h, for h in the range 0.3-1. This slope is neither influenced by the plant species, nor by the environmental conditions where plants grow nor does it show strong variations along long leaves.

  5. A method for determining the nitrogen isotopic composition of porphyrins. (United States)

    Higgins, Meytal B; Robinson, Rebecca S; Casciotti, Karen L; McIlvin, Matthew R; Pearson, Ann


    We describe a new method for analysis of the nitrogen isotopic composition of sedimentary porphyrins. This method involves separation and purification of geoporphyrins from sediment samples using liquid chromatography and HPLC, oxidation of the nitrogen within porphyrin-enriched fractions using a two-step process, and isotopic analysis of the resulting nitrate using the denitrifier method. By analysis of these degradation products of chlorophylls, we are able to measure an isotopic signature that reflects the nitrogen utilized by primary producers. The high sensitivity of the denitrifier method allows measurement of small samples that contain low concentrations of porphyrins. Extraction of only 50 nmol of nitrogen (nmol N) allows the following five analyses to be made (each on approximately 10 nmol N): nitrogen concentration, an assessment of potential contamination by nonporphyrin N, and three replicate isotopic measurements. The measured values of delta15N have an average analytical precision of +/-0.5 per thousand (1sigma) and an average contribution from Rayleigh fractionation of 0.7 per thousand from incomplete oxidation of porphyrin N to nitrate. The overall method will enable high-resolution records of delta15N values to be obtained for geological and ecological applications.


    Energy Technology Data Exchange (ETDEWEB)

    Wimpenny, Josh; Yin, Qing-zhu [Department of Earth and Planetary Sciences, University of California, One Shields Avenue, Davis, CA 95616 (United States); Amelin, Yuri, E-mail: [Research School of Earth Sciences, The Australian National University, Canberra, ACT 0200 (Australia)


    Studies of Lu–Hf isotope systematics in meteorites have produced apparent “ages” that are older than Pb–Pb ages and older than the estimated age of our solar system. One proposed explanation for this discrepancy is that irradiation by cosmic rays caused excitation of {sup 176}Lu to its short-lived isomer that then underwent rapid decay to {sup 176}Hf. This explanation can account for apparent excesses in {sup 176}Hf that correlate with Lu/Hf ratio. Mass balance requires that samples with measurable excess in {sup 176}Hf should also have measurable deficiencies in {sup 176}Lu on the order of 1‰–3‰. To unambiguously test the accelerated decay hypothesis, we have measured the {sup 176}Lu/{sup 175}Lu ratio in terrestrial materials and achondrites to search for evidence of depletion in {sup 176}Lu. To a precision of 0.1‰ terrestrial standards, cumulate and basaltic eucrites and angrites all have the same {sup 176}Lu/{sup 175}Lu ratio. Barring a subsequent mass-dependent fractionation event, these results suggest that the apparent excesses in {sup 176}Hf are not caused by accelerated decay of {sup 176}Lu, and so another hypothesis is required to explain apparently old Lu–Hf ages.

  7. 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 (United States)

    Xu, Bin; Jiang, Shao-Yong; Luo, Lan; Zhao, Kui-Dong; Ma, Liang


    The Pengshan Sn and Pb-Zn polymetallic deposits are located in the south margin of the Jiujiang-Ruichang (Jiurui) district of the Middle-Lower Yangtze River Metallogenic Belt in South China. Four large deposits include Huangjinwa, Zengjialong, Jianfengpo, and Zhangshiba, the former three are Sn-dominant deposits which occur as stratiform orebodies in the contact zones of the Pengshan granites and within the country rock strata, whereas Zhangshiba consists of stratiform Pb-Zn orebodies within the Precambrian metasedimentary strata. In this study, we present results on zircon U-Pb ages, major and trace elements, and mineral chemistry as well as Sr-Nd-Hf isotope data of the granites, Pb and S isotopes of both the Sn-dominant and Pb-Zn dominant deposits, and U-Pb dating of cassiterite from the Pengshan district. SHRIMP and LA-ICP-MS zircon U-Pb dating shows that the Pengshan granites were emplaced in the Early Cretaceous (129-128 Ma), which is in good agreement with the U-Pb dating (130-128 Ma) of cassiterite from the Jianfengpo Sn deposit. The Pengshan granites consist mainly of weakly peraluminous highly fractionated I-type affinity granitic rocks. Detailed elemental and isotopic data suggest that the granites formed by partial melting of Mesoproterozoic metamorphic basement materials with minor input of mantle-derived melts. The mineral chemistry of biotite demonstrates that the Pengshan granitic magma had a low oxygen fugacity, thereby precluding the tin dominantly partitioning into the rock-forming silicate minerals and favoring accumulation in the exsolved residual liquid during magma crystallization stages. Sulfur isotopes show a relatively heavy sulfur isotopic composition from 5.8 to 17.6 ‰, and no difference for sulfur isotopes between the Sn deposits (5.8-13.4 ‰, Huangjinwa, Zengjialong, Jianfengpo) and the Pb-Zn deposit (mostly 7.1-13.0 ‰, except for one 17.6 ‰, Zhangshiba). The sulfur isotope data of pyrite from the host sedimentary rocks show

  8. 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 (United States)

    Xu, Bin; Jiang, Shao-Yong; Luo, Lan; Zhao, Kui-Dong; Ma, Liang


    The Pengshan Sn and Pb-Zn polymetallic deposits are located in the south margin of the Jiujiang-Ruichang (Jiurui) district of the Middle-Lower Yangtze River Metallogenic Belt in South China. Four large deposits include Huangjinwa, Zengjialong, Jianfengpo, and Zhangshiba, the former three are Sn-dominant deposits which occur as stratiform orebodies in the contact zones of the Pengshan granites and within the country rock strata, whereas Zhangshiba consists of stratiform Pb-Zn orebodies within the Precambrian metasedimentary strata. In this study, we present results on zircon U-Pb ages, major and trace elements, and mineral chemistry as well as Sr-Nd-Hf isotope data of the granites, Pb and S isotopes of both the Sn-dominant and Pb-Zn dominant deposits, and U-Pb dating of cassiterite from the Pengshan district. SHRIMP and LA-ICP-MS zircon U-Pb dating shows that the Pengshan granites were emplaced in the Early Cretaceous (129-128 Ma), which is in good agreement with the U-Pb dating (130-128 Ma) of cassiterite from the Jianfengpo Sn deposit. The Pengshan granites consist mainly of weakly peraluminous highly fractionated I-type affinity granitic rocks. Detailed elemental and isotopic data suggest that the granites formed by partial melting of Mesoproterozoic metamorphic basement materials with minor input of mantle-derived melts. The mineral chemistry of biotite demonstrates that the Pengshan granitic magma had a low oxygen fugacity, thereby precluding the tin dominantly partitioning into the rock-forming silicate minerals and favoring accumulation in the exsolved residual liquid during magma crystallization stages. Sulfur isotopes show a relatively heavy sulfur isotopic composition from 5.8 to 17.6 ‰, and no difference for sulfur isotopes between the Sn deposits (5.8-13.4 ‰, Huangjinwa, Zengjialong, Jianfengpo) and the Pb-Zn deposit (mostly 7.1-13.0 ‰, except for one 17.6 ‰, Zhangshiba). The sulfur isotope data of pyrite from the host sedimentary rocks show

  9. Tellurium isotope compositions of calcium-aluminum-rich inclusions (United States)

    Fehr, M. A.; Rehkämper, M.; Halliday, A. N.; Hattendorf, B.; Günther, D.


    A method for the precise and accurate determination of the tellurium (Te) isotope compositions of calcium-aluminum-rich inclusions (CAIs) has been developed. The technique utilizes multiple-collector inductively coupled plasma-mass spectrometry (MC-ICPMS) with either Faraday detectors or a dual ion-counting system. The external reproducibility (2σ) for 126Te/125Te was ~15‰ and ~2‰ when 3 pg and 65 pg of Te were analyzed with the electron multipliers. Measurements performed on 200 pg of Te using Faraday detectors and time-resolved software displayed an external reproducibility of ~8‰ for 126Te/124Te, whereas 3 ng Te could be measured to a precision of about 0.6‰. Analyses of five CAIs from the Allende chondrite yielded Te concentrations that range from 12 to 537 ppb and the inclusions are therefore depleted in Te relative to bulk Allende by factors of about 2 to 86. The Sn/Te ratios of the CAIs are also fractionated compared to bulk Allende (which displays 124Sn/128Te ≍ 0.1) with 124Sn/128Te ratios of about 0.1 to 2.5. The Te isotope measurements for these refractory inclusions yielded no 126Te excesses from the decay of the short-lived radionuclide 126Sn (τ½ = 234,500 years) and the most precise analysis provided a ɛ126Te value of 1 ± 6 (ɛ126Te = 126Te/ 124Te normalized to 122Te/124Te = 0.53594 and reported relative to the JMC Te standard). Minor differences in the Te isotope composition of the CAIs relative to the terrestrial standard and bulk Allende hint at the presence of small deficits in r-process Te isotopes or excess of s-process Te, but these nucleosynthetic anomalies are barely resolvable given the analytical uncertainties. Hence, it is also conceivable that these effects reflect small unresolved analytical artifacts.

  10. Oxygen isotope composition of mafic magmas at Vesuvius (United States)

    Dallai, L.; Cioni, R.; Boschi, C.; D'Oriano, C.


    The oxygen isotope composition of olivine and clinopyroxene from four plinian (AD 79 Pompeii, 3960 BP Avellino), subplinian (AD 472 Pollena) and violent strombolian (Middle Age activity) eruptions were measured to constrain the nature and evolution of the primary magmas of the last 4000 years of Mt. Vesuvius activity. A large set of mm-sized crystals was accurately separated from selected juvenile material of the four eruptions. Crystals were analyzed for their major and trace element compositions (EPMA, Laser Ablation ICP-MS), and for 18O/16O ratios. As oxygen isotope composition of uncontaminated mantle rocks on world-wide scale is well constrained (δ18Oolivine = 5.2 ± 0.3; δ18Ocpx = 5.6 ± 0.3 ‰), the measured values can be conveniently used to monitor the effects of assimilation/contamination of crustal rocks in the evolution of the primary magmas. Instead, typically uncontaminated mantle values are hardly recovered in Italian Quaternary magmas, mostly due to the widespread occurrence of crustal contamination of the primary magmas during their ascent to the surface (e.g. Alban Hills, Ernici Mts., and Aeolian Islands). Low δ18O values have been measured in olivine from Pompeii eruption (δ18Oolivine = 5.54 ± 0.03‰), whereas higher O-compositions are recorded in mafic minerals from pumices or scoria of the other three eruptions. Measured olivine and clinopyroxene share quite homogeneous chemical compositions (Olivine Fo 85-90 ; Diopside En 45-48, respectively), and represent phases crystallized in near primary mafic magmas, as also constrained by their trace element compositions. Data on melt inclusions hosted in crystals of these compositions have been largely collected in the past demonstrating that they crystallized from mafic melt, basaltic to tephritic in composition. Published data on volatile content of these melt inclusions reveal the coexistence of dissolved water and carbon dioxide, and a minimum trapping pressure around 200-300 MPa, suggesting

  11. Geochronology and Hf Isotope Study of Pegmatite in the Xiaoqinling Area of NW China:Implication for Petrogenesis and Regional Metamorphism

    Institute of Scientific and Technical Information of China (English)

    Haixiang Zhao; Shaoyong Jiang; Baozhang Dai; Liang Ma; Jianwei Li


    In this study, we carried out petrography, zircon U-Pb geochronology and Hf isotopic analyses on a granitic pegmatite dyke in the Xiaoqinling area in southern margin of the North China Craton (NCC). Our study suggests that the pegmatite dyke likely crystallized from a volatile-rich peg-matitic magma. Different from most other pegmatite elsewhere, zircon from this pegmatite dyke does not contain unusually high U and Th concentrations and suffered no evident radioactive damage, therefore we successfully obtained a zircon U-Pb dating using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), which yields an average 207Pb/206Pb age of 1 814±6 Ma, representing the intrusive age of the granitic pegmatite dyke. ZirconεHf(t) values are between-8.3 and-3.0, corresponding to Hf depleted mantle model ages from 2 649 to 2 991 Ma with an average of 2 881 Ma. These data indicate that this granitic pegmatite dyke may have been derived from partial melting of Meso-Neoarchean metamorphic rocks from the Xiaoqinling basement. Granitic pegmatite magma may have emplaced within the Taihua Group wall rocks during the last stage of the middle to high grade metamorphism. Furthermore, according to the petrographic observation, the 1.81 Ga pegmatite dyke and the 1 800–1 750 Ma Xiong’er Group rocks were not undergone middle to high grade meta-morphism, indicating 1.81 Ga as the termination of the latest regional metamorphism in the southern margin of the NCC.

  12. Neoproterozoic granitic magmatism along the Ailao Shan-Red River belt: U-Pb zircon geochronology, Lu-Hf isotopes and tectonic implications (United States)

    Chen, Xiaoyu; Liu, Junlai; Qi, Yinchuan; Fan, Wenkui; Burg, Jean-Pierre


    The Neoproterozoic tectonic characteristics of the high grade metamorphic massifs along the Ailao Shan-Red River belt are debated. Controversies are on 1) whether the massifs were parts of the Yangtze block to the northeast or 2) parts of the Indochina block to the southwest and 3) the magmatic rocks represent arc magmatism or rifting linked to break-up of the Rodinia supercontinent. This study presents new and precise LA-ICP-MS U-Pb age dating and geochemical and Hf isotopic analyses of granitic intrusions along the Ailao Shan-Red River belt in an attempt to elucidate the Neoproterozoic magmatic evolution of this belt. In general, zircon U-Pb ages of the studied granitic rocks are between 804 and 724Ma, with a weighted mean of ca. 770 Ma, thus confirming Neoproterozoic magmatism. All samples plot into the peraluminous domain, indicating a major crustal resource. In consistency with these conclusions, most of the Neoproterozoic granitoids show negative ɛHf (t) values near the chondrite line. A few samples possess low positiveɛ Hf (t) values, being signatures of mantle sources. It is therefore concluded that the Neoproterozoic magmatism along the ASRR belt originated from mantle sources with important contributions through anatexis of ancient lower crust. Discrimination diagrams of tectonic settings suggest continental arc magmatism. Neoproterozoic magmatism is widely reported along the margins of the Yangtze block, especially in the northern margin. However, there are fewer reports about Neoproterozoic magmatic activity along the southern and southwestern margins. The geochronology spectrum and geochemisty of the studied Neoproterozoic granitic rocks are similar to those along the western margin of the Yangtze block. The present study, combined with previous results, suggests that oceanic subduction contributed to the generation of the arc magmatisms along the western and southwestern margin of the Yangtze plate and along the ASRR belt (as part of the

  13. Isotopic Composition of Cosmic Rays:. Results from the Cosmic Ray Isotope Spectrometer on the Ace Spacecraft (United States)

    Israel, M. H.

    Over the past seven years the Cosmic Ray Isotope Spectrometer (CRIS) on the ACE spacecraft has returned data with an unprecedented combination of excellent mass resolution and high statistics, describing the isotopic composition of elements from lithium through nickel in the energy interval ~ 50 to 500 MeV/nucleon. These data have demonstrated: * The time between nucleosynthesis and acceleration of the cosmic-ray nuclei is at least 105 years. The supernova in which nucleosynthesis takes place is thus not the same supernova that accelerates a heavy nucleus to cosmic-ray energy. * The mean confinement time of cosmic rays in the Galaxy is 15 Myr. * The isotopic composition of the cosmic-ray source is remarkably similar to that of solar system. The deviations that are observed, particularly at 22Ne and 58Fe, are consistent with a model in which the cosmic-ray source is OB associations in which the interstellar medium has solar-system composition enriched by roughly 20% admixture of ejecta from Wolf-Rayet stars and supernovae. * Cosmic-ray secondaries that decay only by electron capture provide direct evidence for energy loss of cosmic rays as they penetrate the solar system. This invited overview paper at ECRS 19 was largely the same as an invited paper presented a month earlier at the 8th Nuclei in the Cosmos Conference in Vancouver. The proceedings of that conference will be published shortly by Elsevier as a special edition of Nuclear Physics A. For further summary of results from CRIS, the reader is referred to URL and links on that page to CRIS and to Science News.

  14. Devonian alkaline magmatism in the northern North China Craton: Geochemistry, SHRIMP zircon U-Pb geochronology and Sr-Nd-Hf isotopes

    Directory of Open Access Journals (Sweden)

    Dingling Huang


    Full Text Available The Wulanhada pluton is among the rare suite of Devonian alkaline plutons occurring along the northern margin of the North China Craton (NCC. The intrusion is mainly composed of quartz-monzonite. Here we report zircon SHRIMP U-Pb data from this intrusion which shows emplacement age of ca. 381.5 Ma. The rock is metaluminous with high (Na2O + K2O values ranging from 8.46 to 9.66 wt.%. The REE patterns of the rocks do not show any Eu anomaly whereas the primitive-mantle-normalized spider diagram shows strong positive Sr and Ba anomalies. The Wulanhada rocks exhibit high initial values of (87Sr/86Srt = 0.70762–0.70809, low ɛNd(t = −12.76 to −12.15 values and negative values of ɛHf(t = −23.49 to −17.02 with small variations in (176Hf/177Hft (0.281873–0.282049. These geochemical features and quantitative isotopic modeling results suggest that the rocks might have been formed through the partial melting of Neoarchean basic rocks in the lower crust of the NCC. The Wulanhada rocks, together with the Devonian alkaline rocks and mafic-ultramafic complex from neighboring regions, constitute a post-collisional magmatic belt along the northern NCC.

  15. Isotopic composition and origin of the precipitation in Northern Chile

    Energy Technology Data Exchange (ETDEWEB)

    Aravena, R. [Department of Earth Sciences, University of Waterloo, Waterloo (Canada); Suzuki, O. [Exploracion y Desarrollo de Recursos Hidricos, Santiago (Chile); Pena, H. [Direccion General de Aguas, Ministerio de Obras Publicas, Santiago (Chile); Pollastri, A. [Comision Chilena de Energia Nuclear, Santiago (Chile); Fuenzalida, H. [Departamento de Geofisica, Universidad of Chile, Santiago (Chile); Grilli, A. [Empresa Metropolitana de Obras Sanitarias, Santiago (Chile)


    A 3 a data set of isotopes in precipitation from northern Chile show a very distinct pattern, with {delta}{sup 18}O values ranging between -18 and -15per thousand at high altitude stations, compared to {delta}{sup 18}O values between -10 and -6per thousand at the lower altitude areas. The {sup 18}O-depleted values observed in the high altitude area, the Altiplano, are related to processes that affect the air masses that originated over the Atlantic, cross the Amazon Basin (continental effect), ascend the Andes (altitude effect) and precipitated (convective effect) in the Altiplano. It is postulated that a second source of moisture, associated with air masses from the Pacific, may contribute to the {sup 18}O-enriched values observed in the lower altitude areas. Similar isotopic patterns are documented in springs and groundwater indicating that the data presented in this paper are an accurate representation of the long term behavior isotopic composition of rain in northern Chile. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

  16. On the isotopic composition of magmatic carbon in SNC meteorites (United States)

    Wright, I. P.; Grady, M. M.; Pillinger, C. T.


    SNC meteorites are thought, from many lines of evidence, to come from Mars. A line of investigation which has been pursued in our laboratory over the years involves measurement of the stable isotopic composition of carbon, in its various forms, in SNC meteorites. In order to establish a firm basis for studying the isotopic systematics of carbon in the martian surface environment, it is first necessary to try and constrain the delta C-13 of bulk Mars. Taking all of the available information, it would seem that the delta C-13 of the Earth's mantle lies somewhere in the range of -5 to -7 percent. Preliminary assessment of magnetic carbon in SNC meteorites, would tend to suggest a delta C-13 of 20 to 30 percent, which is conspicuously different from that of the terrestrial mantle. It is not obvious why there should be such a difference between the two planets, although many explanations are possible. One of these possibilities, that previous delta C-13 measurements for magnetic carbon in SNC meteorites are in error to some degree, is being actively investigated. The most recent results seem to constrain the theta C-13 of the magnetic carbon in SNC meteorites to about -20 percent, which is not at odds with previous estimates. As such, it is considered that a detailed investigation of the carbon isotopic systematics of martian surface materials does have the necessary information with which to proceed.

  17. Crustal basement controls granitoid magmatism, and implications for generation of continental crust in subduction zones: A Sr-Nd-Hf-O isotopic study from the Paleozoic Tongbai orogen, central China (United States)

    Wang, Hao; Wu, Yuan-Bao; Yang, Jin-Hui; Qin, Zheng-Wei; Duan, Rui-Chun; Zhou, Lian; Yang, Sai-Hong


    Ascertaining the petrogenesis of granitoid rocks in subduction zones holds the key for understanding the processes of how continental crust is produced. The synchronous Taoyuan and Huanggang plutons occur in two different geological units of the Paleozoic Tongbai orogen of central China. They provide an optimal opportunity for a study to address the role of the crustal basement in generating voluminous granitoid magmatism in subduction zones. The Taoyuan and Huanggang plutons have identical U-Pb zircon crystallization ages of 440-444 Ma, which are temporally related to northward subduction of the Paleotethyan Ocean. The Taoyuan samples show high SiO2 (73.36-79.16%) and low Al2O3 (12.00-13.45%) contents, Mg numbers (20.6-38.2), and Sr/Y (2.04-10.1) and (La/Yb)N (2.34-7.32) ratios with negative Eu anomalies (Eu/Eu* = 0.33-0.93). They yielded positive εNd(t) (+ 3.0 to + 6.7) and εHf(t) (+ 11.8 to + 13.2) values, elevated initial Sr isotopic ratios (0.7040-0.7057) and relatively low zircon δ18O values of 4.62-5.39‰. These suggest that they were produced through partial melting of hydrothermally altered lower crust of the accreted Erlangping oceanic arc. In contrast, the Huanggang samples exhibit variable whole-rock geochemical and isotopic compositions with SiO2 contents of 57.01-64.42 wt.%, initial Sr isotopic ratios of 0.7065-0.7078, and εNd(t) values of - 5.7 to - 9.4. Additionally, they have high zircon δ18O values of 7.57-8.45‰ and strongly negative zircon εHf(t) values of - 14.4 to - 10.5. They were suggested to have been mainly derived from ancient continental crust of the Kuanping crustal unit with the addition of 20-40% juvenile, mantle-derived material. Accordingly, the granitoids in both oceanic and continental arcs are likely to be mainly derived from intracrustal melting of their crustal basement. It is revealed by the Huanggang pluton that little net continental crust growth occurs in continental arcs, and addition of new volume of continental

  18. Petrogenesis of highly fractionated I-type granites in the Zayu area of eastern Gangdese, Tibet: Constraints from zircon U-Pb geochronology, geochemistry and Sr-Nd-Hf isotopes

    Institute of Scientific and Technical Information of China (English)


    The Cretaceous granitoids in the middle and northern Gangdese, Tibet are generally interpreted as the products of anatexis of thickened deep crust genetically associated with the Lhasa-Qiangtang collision. This paper reports bulk-rock major element, trace element and Sr-Nd isotopic data, zircon U-Pb age data, and zircon Hf isotopic data on the Zayu pluton in eastern Gangdese, Tibet. These data shed new light on the petrogenesis of the pluton. Our SHRIMP zircon U-Pb age dates, along with LA-ICPMS zircon U-Pb age dates recently reported in the literature, indicate that the Zayu pluton was emplaced at about 130 Ma, coeval with Early Cretaceous magmatic rocks in other areas of eastern Gangdese (e.g., Rawu, Baxoi areas) and the Middle Gangdese. The Zayu pluton samples lack amphibole and muscovite, and are compositionally characterized by high SiO2 (69.9%―76.8%), K2O (4.4%―5.7%), and low P2O5 (0.05%―0.12%). These samples also have A/CNK values of 1.00-1.05, and are enriched in Rb, Th, U, and Pb, and depleted in Ba, Nb, Ta, Sr, P, Ti, and Eu. These geochemical features suggest that the Zayu pluton samples are metaluminous to slightly peraluminous and are of highly fractionated I-type granite. The Zayu pluton samples have high εNd(t) values (-10.9--7.6) and low initial 87Sr/86Sr ratios (0.7120- 0.7179) relative to melts derived from mature continental crust in the Gangdese (e.g., Ningzhong Early Jurassic strongly peraluminous granite). The Zayu pluton samples are heterogeneous in zircon εHf(t) values (-12.8--2.9), yielding ancient zircon Hf crustal model ages of 1.4―2.0 Ga. The data obtained in this study together with the data in the recent literature suggest that the Early Cretaceous granitoids in eastern Gangdese represent the eastward extension of the Early Cretaceous magmatism in the middle Gangdese, and that the Lhasa micro-continent block with ancient basement may extend for ~2000 km from east to west. Zircon Hf isotopic data and bulk-rock zircon

  19. Petrogenesis of highly fractionated Ⅰ-type granites in the Zayu area of eastern Gangdese,Tibet:Constraints from zircon U-Pb geochronology,geochemistry and Sr-Nd-Hf isotopes

    Institute of Scientific and Technical Information of China (English)

    ZHU DiCheng; MO XuanXue; WANG LiQuan; ZHAO ZhiDan; NIU Yaoling; ZHOU ChangYong; YANG YueHeng


    The Cretaceous granitoids in the middle and northern Gangdese,Tibet are generally interpreted as the products of anatexis of thickened deep crust genetically associated with the Lhasa-Qiangtang collision.This paper reports bulk-rock major element,trace element and Sr-Nd isotopic data,zircon U-Pb age data,and zircon Hf isotopic data on the Zayu pluton in eastern Gangdese,Tibet.These data shed new light on the petrogenesis of the pluton.Our SHRIMP zircon U-Pb age dates,along with LA-ICPMS zircon U-Pb age dates recently reported in the literature,indicate that the Zayu pluton was emplaced at about 130 Ma,coeval with Early Cretaceous magmatic rocks in other areas of eastern Gangdese (e.g.,Rawu,Baxoi areas) and the Middle Gangdese.The Zayu pluton samples lack amphibole and muscovite,and are compositionally characterized by high SiO2 (69.9%-76.8%),K20 (4.4%-5.7%),and low P2O5 (0.05%-0.12%).These samples also have A/CNK values of 1.00-1.05,and are enriched in Rb,Th,U,and Pb,and depleted in Ba,Nb,Ta,Sr,P,Ti,and Eu.These geochemical features suggest that the Zayu pluton samples ere metaluminous to slightly peraluminous and are of highly fractionated Ⅰ-type granite.The Zayu pluton samples have high εNd(t) values (-10.9-7.6) and low initial 87Sr/86Sr ratios (0.7120-0.7179) relative to melts derived from mature continental crust in the Gangdese (e.g.,Ningzhong Early Jurassic strongly peraluminous granite).The Zayu pluton samples are heterogeneous in zircon εHf(t) values (-12.8-2.9),yielding ancient zircon Hf crustal model ages of 1.4-2.0 Ga.The data obtained in this study together with the data in the recent literature suggest that the Early Cretaceous granitoids in eastern Gangdese represent the eastward extension of the Early Cretaceous magmatism in the middle Gangdese,and that the Lhasa micro-continent block with ancient basement may extend for ~2000 km from east to west.Zircon Hf isotopic data and bulk-rock zircon saturation temperature (789-821℃) indicate that

  20. Stable carbon isotopic composition of gasolines determined by isotope ratio monitoring gas chromatography mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Smallwood, B.J.; Philp, R.P.; Allen, J.D. [University of Oklahoma, Norman, OK (United States). School of Geology and Geophysics


    A large number of underground gasoline storage facilities in the United States continuously leak gasoline into the subsurface, which makes gasoline a major groundwater contaminant. Gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS) are used currently to characterize contaminated groundwater and soils. Correlations of contaminants with suspected source(s) are extremely difficult by these techniques because many gasolines have similar hydrocarbon distributions. The present study applied the technique of isotope ratio monitoring gas chromatography-mass spectrometry (irmGC-MS) to 19 gasoline samples from different areas of the USA. This allows a much better correlation of gasoline contaminants to source. Data obtained indicate a wide range of {sup {delta}}{sup 13}C values for 16 ubiquitous compounds in the gasolines. The majority of samples could be distinguished from each other on the basis of {sup {delta}}{sup 13}C hydrocarbon composition. The oxygenated additive methyl tertiary butyl ether (MTBE) was present in ten of the gasolines analyzed, and had a relatively narrow range of {sup {delta}}{sup 13}C values (-30.4 to -28.3 per mille). Preliminary investigations were also made to determine the extent of carbon isotopic fractionation after simple water washing and evaporation experiments. Results indicate that the majority of compounds did not undergo significant carbon isotopic fractionation as a result of these processes. (author)

  1. Recent insights into intramolecular 13C isotope composition of biomolecules (United States)

    Gilbert, A.; Yamada, K.; Julien, M.; Yoshida, N.; Remaud, G.; Robins, R.


    In 1961 Abelson & Hoering shown that the intramolecular 13C distribution in amino acids was not homogeneous, namely the carboxylic acid positions were 13C-enriched compared with the mean of the remaining C-atoms in the molecule [1]. Nearly 20 years later, Monson & Hayes were able to demonstrate that even and odd positions in acetogenic fatty acids also showed non-statistical 13C isotope distributions, and that the pattern varied depending on the organism [2]. It took a further decade for the intramolecular 13C distribution in the key metabolite, glucose, to be defined [3]. Although informative, much of this work was incomplete, a number of positions having to be deduced by difference. This limitation arose mainly due to the lack of techniques enabling the separation and quantification of 13C isotopomers of the target molecule. In the past decade, quantitative 13C NMR has been developed for the determination of the intramolecular isotope composition of a given molecule with a precision of 1‰ or better [4]. This breakthrough has made possible a comprehensive view of the determinants governing intramolecular isotope composition of biological molecules. In particular, it can be shown that intramolecular pattern in sugars is influenced by the C-assimilation pathway and by post-photosynthetic fractionation associated with carbohydrate metabolism [5]. In addition, analysis by NMR of the alkyl chain of acetogenic lipids (fatty acids, n-alkanes) shows an alternation between odd and even C-atom positions, as observed by Monson& Hayes [2], throughout the molecule [6]. Overall, it is becoming apparent that this pattern is influenced by two principal metabolic factors: (i) the 13C pattern extant in the starting compounds; (ii) isotope fractionation associated with the enzymes involved in the biosynthetic pathway. On the whole, the determination of intramolecular isotope patterns in biomolecules allows better insights into the conditions and pathways by which they are formed

  2. Isotope composition of bicarbonate carbon in bed waters of oil and gas deposits

    Energy Technology Data Exchange (ETDEWEB)

    Golyshev, S.I.; Cherepnin, A.V.; Ivanov, V.G.; Manylova, L.S.


    A study is made of the isotope composition of bicarbonate carbon in bed waters of the Jurassic water complex in southeast West Siberia. It has been established that waters of empty and transcontour structures have isotope composition of carbon 5/sup 0//oo, while in waters which contact the hydrocarbon formations, the isotope composition of carbon is lighter on the average by 5-8/sup 0//oo. The isotope composition of bicarbonate carbon in bed waters reflects both the conditions for primary sedimentation, and secondary processes associated with organic matter transformation.

  3. Palaeoproterozoic continental arc magmatism, and Neoproterozoic metamorphism in the Aravalli-Delhi orogenic belt, NW India: New constraints from in situ zircon U-Pb-Hf isotope systematics, monazite dating and whole-rock geochemistry (United States)

    Kaur, Parampreet; Zeh, Armin; Chaudhri, Naveen


    Presently, the extent, origin and petrogenesis of late Palaeoproterozoic (ca. 1.85 Ga) magmatism in the north-central Aravalli-Delhi orogenic belt, NW India and subsequent metamorphic overprints are poorly constrained. Results of new in situ zircon U-Pb-Hf isotope analyses in combination with whole-rock elemental and isotopic data provide the first hard evidence that granitoid magmatism occurred in a continental magmatic arc setting between 1.86 and 1.81 Ga. The Hf-Nd model ages of 3.0-2.6 Ga and inherited zircon grains of 3.3-2.5 Ga indicate abundant reworking of Archaean crust. Flat HREE patterns with negative Eu anomalies furthermore reveal that the granitoids were generated from garnet-free and plagioclase-rich sources at shallow depths. Significant isotope variation among granitoid samples (εHft = -3.7 to -9.0; εNdt = -4.8 to -7.9) indicate that the reworked Archaean crust was not completely homogenised during the Palaeoproterozoic. This is best reflected by zircon Hf-isotope variation of ca. 9.5 epsilon units within the oldest granitoid sample. Zircon grains from this sample define three discrete Hf-isotope groups at εHf1.86Ga = -8.9, -4.8 and -1.6. These are interpreted to result from mixing of zircon-saturated magmas derived from three distinct sources within the crust prior to solidification. A monazite U-Pb isochron age of 868 ± 4 Ma from one of the granitoid samples furthermore indicates that the Aravalli fold belt was affected by an important post-magmatic overprint, perhaps related to the widespread metasomatic, granulite metamorphic and/or magmatic events during the same time span.

  4. Origin of Meso-Proterozoic post-collisional leucogranite suites (Kaokoveld, Namibia): constraints from geochronology and Nd, Sr, Hf, and Pb isotopes (United States)

    Jung, S.; Mezger, K.; Nebel, O.; Kooijman, E.; Berndt, J.; Hauff, F.; Münker, C.


    Leucocratic granites of the Proterozoic Kaoko Belt, northern Namibia, now preserved as meta-granites, define a rock suite that is distinct from the surrounding granitoids based on their chemical and isotopic characteristics. Least evolved members of this ~1.5-1.6-Ga-old leucogranite suite can be distinguished from ordinary calc-alkaline granites that occur elsewhere in the Kaoko Belt by higher abundances of Zr, Y, and REE, more radiogenic initial ɛNd values and unradiogenic initial 87Sr/86Sr. The leucogranites have high calculated zircon saturation temperatures (mostly > 920°C for least fractionated samples), suggesting that they represent high-temperature melts originating from deep crustal levels. Isotope data (i.e., ɛNdi: +2.3 to -4.2) demonstrate that the granites formed from different sources and differentiated by a variety of processes including partial melting of mantle-derived meta-igneous rocks followed by crystal fractionation and interaction with older crustal material. Most fractionation-corrected Nd model ages (TDM) are between 1.7 and 1.8 Ga and only slightly older than the inferred intrusion age of ca. 1.6 Ga, indicating that the precursor rocks must have been dominated by juvenile material. Epsilon Hf values of zircon separated from two granite samples are positive (+11 and +13), and Hf model ages (1.5 and 1.6 Ga) are similar to the U-Pb zircon ages, again supporting the dominance of juvenile material. In contrast, the Hf model ages of the respective whole rock samples are 2.3 and 2.4 Ga, demonstrating the involvement of older material in the generation of the granites. The last major tectonothermal event in the Kaoko Belt in the Proterozoic occurred at ca. 2.0 Ga and led to reworking of mostly 2.6-Ga-old rocks. However, the presence of 1.6 Ga "post-collisional" granites reflects addition of some juvenile mantle-derived material after the last major tectonic event. The results suggest that similar A-type leucogranites are potentially more

  5. Zircon U-Pb geochronology, geochemistry, and Sr-Nd-Hf isotopes of granitoids in the Yulekenhalasu copper ore district, northern Junggar, China: Petrogenesis and tectonic implications (United States)

    Yang, Fuquan; Chai, Fengmei; Zhang, Zhixin; Geng, Xinxia; Li, Qiang


    The Yulekenhalasu porphyry copper deposit is located in the Kalaxiange'er metallogenic belt in northern Junggar, China. We present the results from zircon U-Pb geochronology, and geochemical and Sr-Nd-Hf isotope analyses of the granitoids associated with the ore deposits with a view to constrain their petrogenesis and tectonic setting. The granitoids consist of quartz diorite, diorite porphyry, porphyritic monzonite, and quartz porphyry, emplaced at 382, 379, 375-374, and 348 Ma, respectively, which span Late Devonian to early Carboniferous ages. The ore-bearing intrusion is mainly diorite porphyry, with subordinate porphyritic monzonite. The Late Devonian intrusions are characterized by SiO2 contents of 54.5-64.79 wt.%, Na2O contents of 3.82-8.24 wt.%, enrichment in Na, light rare-earth elements (LREEs), and large ion lithophile elements. They also display relative depletion in Y, Ba, P, Nb, Ta, and Ti, and weak negative Eu anomalies (δEu = 0.6-0.87). The early Carboniferous quartz porphyry is characterized by high SiO2 content (72.26-73.35 wt.%), enrichment in LREEs, K, and Sr, and relative depletion in Y (10.82-12.52 ppm) and Yb (1.06-1.15 ppm). The Late Devonian and early Carboniferous granitoids are characterized by positive ɛNd(t) values (5.2-10.1, one sample at - 1.9), positive ɛHf(t) values (7.46-18.45), low (87Sr/86Sr)i values (0.70363-0.70476), and young crustal residence ages. These data indicate that the sources of the granitoids were mainly mantle-derived juvenile rocks. Geochemical and Nd-Sr-Hf isotopic data demonstrate that the Late Devonian granitoids formed in an oceanic island arc, and they were formed from different sources, among which the mineralized diorite porphyry might have originated from a mixed slab-derived and mantle wedge melt source. The early Carboniferous quartz porphyry was likely emplaced in a mature island arc environment, and was probably derived from juvenile crust.

  6. U-Pb ages, geochemistry, C-O-Nd-Sr-Hf isotopes and petrogenesis of the Catalão II carbonatitic complex (Alto Paranaíba Igneous Province, Brazil): implications for regional-scale heterogeneities in the Brazilian carbonatite associations (United States)

    Guarino, Vincenza; Wu, Fu-Yuan; Melluso, Leone; de Barros Gomes, Celso; Tassinari, Colombo Celso Gaeta; Ruberti, Excelso; Brilli, Mauro


    The Catalão II carbonatitic complex is part of the Alto Paranaíba Igneous Province (APIP), central Brazil, close to the Catalão I complex. Drill-hole sampling and detailed mineralogical and geochemical study point out the existence of ultramafic lamprophyres (phlogopite-picrites), calciocarbonatites, ferrocarbonatites, magnetitites, apatitites, phlogopitites and fenites, most of them of cumulitic origin. U-Pb data have constrained the age of Catalão I carbonatitic complex between 78 ± 1 and 81 ± 4 Ma. The initial strontium, neodymium and hafnium isotopic data of Catalão II (87Sr/86Sri = 0.70503-0.70599; ɛNdi = -6.8 to -4.7; 176Hf/177Hf = 0.28248-0.28249; ɛHfi = -10.33 to -10.8) are similar to the isotopic composition of the Catalão I complex and fall within the field of APIP kimberlites, kamafugites and phlogopite-picrites, indicating the provenance from an old lithospheric mantle source. Carbon isotopic data for Catalão II carbonatites (δ13C = -6.35 to -5.68 ‰) confirm the mantle origin of the carbon for these rocks. The origin of Catalão II cumulitic rocks is thought to be caused by differential settling of the heavy phases (magnetite, apatite, pyrochlore and sulphides) in a magma chamber repeatedly filled by carbonatitic/ferrocarbonatitic liquids ( s.l.). The Sr-Nd isotopic composition of the Catalão II rocks matches those of APIP rocks and is markedly different from the isotopic features of alkaline-carbonatitic complexes in the southernmost Brazil. The differences are also observed in the lithologies and the magmatic affinity of the igneous rocks found in the two areas, thus demonstrating the existence of regional-scale heterogeneity in the mantle sources underneath the Brazilian platform.

  7. In situ isotopic analyses of U and Pb in zircon by remotely operated SHRIMP II, and Hf by LA-ICP-MS: an example of dating and genetic evolution of zircon by {sup 176}Hf/{sup 177}Hf from the Ita Quarry in the Atuba Complex, SE, Brazil; Analises in situ de U e Pb em zircao por SRIMP II por controle remoto e de Hf por LA-ICP-MS: um exemplo de datacao e da evolucao genetica de zircao atraves da razao {sup 176}Hf/{sup 177} em amostra da Pedreira Ita no Complexo Atuba, SE, Brasil

    Energy Technology Data Exchange (ETDEWEB)

    Sato, K.; Siga Junior, Oswaldo; McReath, Ian; Sproesser, Walter; Basei, Miguel Angelo Stipp [Universidade de Sao Paulo (USP), SP (Brazil). Inst. de Geociencias. Centro de Pesquisas Geocronologicas], e-mail:, e-mail:, e-mail:, e-mail:, e-mail:; Silva, Josiane Aline da [Universidade de Sao Paulo (USP), SP (Brazil). Programa de Pos-graduacao em Geoquimica e Geotectonica; Dunyi, Liu [Institute of Geology, Beijing (China); Iizuka, Takafumi; Rino, Shuji; Hirata, Takafumi [Tokyo Institute of Technology, Tokyo (Japan)


    Remotely-operated SHRIMP dating of zircon is an interesting alternative for dating of zircon crystals. Although it does not represent any technical progress of the geochronological method using the U-Pb system in zircon it is a very useful and cheap facility. The procedure was first used for mass spectrometric analyses involving two international laboratories in Sao Paulo, Brazil and Beijing, China. It was applied to samples of three gneiss-migmatitic rocks from the Ita quarry in the Atuba Complex (located between the Luis Alves and the Apiai Domain) to test previous controversial hypotheses about its evolution. The presence of important archaean and paleo proterozoic components in the complex is confirmed by analyses of zircon found in probably neo proterozoic leucosomes. Diorite intrusion also occurred during the neo proterozoic, associated with the 0.6Ga continental collisions involved in the assembly of Gondwana. The determination of Hf isotope ratios by LA-ICP/MS represents a new option for checking the relative importance of mantle ({epsilon}{sub Hf} > 0) and crustal contributions (({epsilon}{sub Hf} < 0) during the growth of the zircon crystals. While the archaean component in the complex was derived from the mantle ({epsilon}{sub Hf} + 1.5 to + 8.7) the paleo proterozoic component had a crustal contribution ({epsilon}{sub Hf} - 9.1 to -10.1). (author)

  8. The chlorine isotopic composition of Martian meteorites 1: Chlorine isotope composition of Martian mantle and crustal reservoirs and their interactions (United States)

    Williams, J. T.; Shearer, C. K.; Sharp, Z. D.; Burger, P. V.; McCubbin, F. M.; Santos, A. R.; Agee, C. B.; McKeegan, K. D.


    The Martian meteorites record a wide diversity of environments, processes, and ages. Much work has been done to decipher potential mantle sources for Martian magmas and their interactions with crustal and surface environments. Chlorine isotopes provide a unique opportunity to assess interactions between Martian mantle-derived magmas and the crust. We have measured the Cl-isotopic composition of 17 samples that span the range of known ages, Martian environments, and mantle reservoirs. The 37Cl of the Martian mantle, as represented by the olivine-phyric shergottites, NWA 2737 (chassignite), and Shergotty (basaltic shergottite), has a low value of approximately -3.8‰. This value is lower than that of all other planetary bodies measured thus far. The Martian crust, as represented by regolith breccia NWA 7034, is variably enriched in the heavy isotope of Cl. This enrichment is reflective of preferential loss of 35Cl to space. Most basaltic shergottites (less Shergotty), nakhlites, Chassigny, and Allan Hills 84001 lie on a continuum between the Martian mantle and crust. This intermediate range is explained by mechanical mixing through impact, fluid interaction, and assimilation-fractional crystallization.

  9. Continuous measurements of isotopic composition of water vapour on the East Antarctic Plateau (United States)

    Casado, Mathieu; Landais, Amaelle; Masson-Delmotte, Valérie; Genthon, Christophe; Kerstel, Erik; Kassi, Samir; Arnaud, Laurent; Picard, Ghislain; Prie, Frederic; Cattani, Olivier; Steen-Larsen, Hans-Christian; Vignon, Etienne; Cermak, Peter


    Water stable isotopes in central Antarctic ice cores are critical to quantify past temperature changes. Accurate temperature reconstructions require one to understand the processes controlling surface snow isotopic composition. Isotopic fractionation processes occurring in the atmosphere and controlling snowfall isotopic composition are well understood theoretically and implemented in atmospheric models. However, post-deposition processes are poorly documented and understood. To quantitatively interpret the isotopic composition of water archived in ice cores, it is thus essential to study the continuum between surface water vapour, precipitation, surface snow and buried snow. Here, we target the isotopic composition of water vapour at Concordia Station, where the oldest EPICA Dome C ice cores have been retrieved. While snowfall and surface snow sampling is routinely performed, accurate measurements of surface water vapour are challenging in such cold and dry conditions. New developments in infrared spectroscopy enable now the measurement of isotopic composition in water vapour traces. Two infrared spectrometers have been deployed at Concordia, allowing continuous, in situ measurements for 1 month in December 2014-January 2015. Comparison of the results from infrared spectroscopy with laboratory measurements of discrete samples trapped using cryogenic sampling validates the relevance of the method to measure isotopic composition in dry conditions. We observe very large diurnal cycles in isotopic composition well correlated with temperature diurnal cycles. Identification of different behaviours of isotopic composition in the water vapour associated with turbulent or stratified regime indicates a strong impact of meteorological processes in local vapour/snow interaction. Even if the vapour isotopic composition seems to be, at least part of the time, at equilibrium with the local snow, the slope of δD against δ18O prevents us from identifying a unique origin leading

  10. Perchlorate in The Great Lakes: Distribution, Isotopic Composition and Origin (United States)

    Poghosyan, A.; Sturchio, N. C.; Jackson, W. A.; Guan, Y.; Eiler, J. M.; Hatzinger, P. B.


    Concentrations, stable chlorine and oxygen isotopic compositions, and 36Cl abundances of perchlorate were investigated in the five Laurentian Great Lakes. Samples were collected during monitoring cruises in 2007 and 2008 of the U.S. EPA's RV Lake Guardian and in 2010 at the water supply intake of Marquette, MI on the southern shore of Lake Superior. Concentrations of perchlorate were measured by IC/MS/MS at 24 locations, including one or two depth profiles in each lake. Mean concentrations (μg/L) are: Superior, 0.06 × 0.01; Michigan, 0.10 × 0.01; Huron, 0.11 × 0.01; Erie, 0.08 × 0.01, and Ontario, 0.09 × 0.01. Concentration vs. depth is nearly constant in each lake, indicating well-mixed conditions. Perchlorate was extracted from near-surface water by passing 15,000 to 80,000 L of water through 1-L cartridges containing Purolite A530E bifunctional anion-exchange resin. In the laboratory, perchlorate was eluted from the resin, purified, and precipitated as a >99% pure crystalline phase. Milligram amounts were recovered from each lake. Chlorine and oxygen isotopic analyses were performed at Caltech using the Cameca 7f-GEO SIMS instrument, following validation of the SIMS method with analyses of USGS-37 and USGS-38 isotopic reference materials. Results indicate a relatively narrow range in δ37Cl values (+2.9 to +3.9 ‰) and a wider range in δ18O values (-4.0 to +4.1 ‰), with a general geographic trend of increasing δ18O from west to east. Oxygen-17 was measured at UIC using dual-inlet IRMS of O2 produced by decomposition of KClO4. Great Lakes perchlorate has mass-independent oxygen isotopic variations with positive Δ17O values (+1.6 ‰ to +2.7 ‰) divided into two distinct groups: Lake Superior (+2.7 ‰) and the other four lakes (~ +1.7 ‰). The isotopic data indicate that perchlorate is dominantly of natural origin, having stable isotopic compositions resembling those of perchlorate from pre-industrial groundwaters in the western USA. The 36Cl

  11. Diagenetic and Metallogenic Sources of Furong Tin Deposit,Qitianling:Constraints from Lu-Hf for Zircon and He-Ar Isotope for Fluid Inclusions%骑田岭芙蓉锡矿的成岩和成矿物质来源:锆石Lu-Hf 同位素和矿物包裹体He-Ar同位素证据

    Institute of Scientific and Technical Information of China (English)

    单强; 曾乔松; 李建康; 卢焕章; 侯茂洲; 于学元; 吴传军


    Determination of zircon U-Pb isotopic date and Lu-Hf isotopic composition of various granitoids in the Qitianling plutons,south China show,there are two-staged granites:the earlier hornblende granitite with 160.0 ±2.7 Ma of zircon U-Pb concordant age and the later granitite with 156.5 ±1.8 Ma of zircon U-Pb concordant age.Metamietimation of zircons appear in the later mineralizing granitite,those zircon is intensively riched in LREE,U and Th,and characteristics of hydrothermal zircon.Lu-Hf isotopic compositions of zircons from four granites show that diagenetic substance are derived from the lower crust, which original magmas were resulted from partial melting of the lower crust in the palaeo-Proterzoic(1 .3~1 .5 Ga),with some mantle substance adding.He-Ar isotopic compositions for fluid inclusions of pyrite and garnet from the Qitianling Furong tin deposit also show a lower ratio of 3 He/4 He(0.059~0.432), which ranges from those between the crust and mantle, suggests mantle fluids are involved in mineralization for the deposit (less than 10% for the amount).%本文分析测试了骑田岭花岗岩芙蓉锡矿的各类花岗岩的锆石 U-Pb 同位素年龄和Lu-Hf同位素组成。本区有两期花岗岩,早期角闪石黑云母花岗岩锆石U-Pb谐和年龄为160.0±2.7 Ma,晚期黑云母花岗岩的锆石U-Pb谐和年龄为156.5±1.8 Ma。在晚期矿化的黑云母花岗岩中出现了蜕晶化锆石,蜕晶化锆石强烈富集LREE和U、Th,是典型热液锆石的特征。四个花岗岩锆石的Lu-Hf同位素组成说明骑田岭花岗岩的成岩物质主要来源于下地壳,它们的原始岩浆源于中元古代(1.3~1.5 Ga)下地壳物质的部分熔融,并有部分地幔物质的参与。还分析测定了骑田岭芙蓉锡矿黄铁矿、石榴子石流体包裹体的 He-Ar 同位素组成,其3 He/4 He 比值较低(0.059~0.432),介于地壳和地幔流体3 He/4 He 比值之间,表明芙蓉锡矿的成

  12. Spectroscopic metrology for isotope composition measurements and transfer standards (United States)

    Anyangwe Nwaboh, Javis; Balslev-Harder, David; Kääriäinen, Teemu; Richmond, Craig; Manninen, Albert; Mohn, Joachim; Kiseleva, Maria; Petersen, Jan C.; Werhahn, Olav; Ebert, Volker


    The World Meteorological Organization (WMO) has identified greenhouse gases such as CO2, CH4 and N2O as critical for global climate monitoring. Other molecules such as CO that has an indirect effect of enhancing global warming are also monitored. WMO has stated compatibility goals for atmospheric concentration and isotope ratio measurements of these gases, e.g. 0.1 ppm for CO2 concentration measurements in the northern hemisphere and 0.01 ‰ for δ13C-CO2. For measurements of the concentration of greenhouse gases, gas analysers are typically calibrated with static gas standards e.g. traceable to the WMO scale or to the International System of Units (SI) through a national metrology institute. However, concentrations of target components, e.g. CO, in static gas standards have been observed to drift, and typically the gas matrix as well as the isotopic composition of the target component does not always reflect field gas composition, leading to deviations of the analyser response, even after calibration. The deviations are dependent on the measurement technique. To address this issue, part of the HIGHGAS (Metrology for high-impact greenhouse gases) project [1] focused on the development of optical transfer standards (OTSs) for greenhouse gases, e.g. CO2 and CO, potentially complementing gas standards. Isotope ratio mass spectrometry (IRMS) [2] is currently used to provide state-of-the-art high precision (in the 0.01 ‰ range) measurements for the isotopic composition of greenhouse gases. However, there is a need for field-deployable techniques such as optical isotope ratio spectroscopy (OIRS) that can be combined with metrological measurement methods. Within the HIGHGAS project, OIRS methods and procedures based on e.g. cavity enhanced spectroscopy (CES) and tunable diode laser absorption spectroscopy (TDLAS), matched to metrological principles have been established for the measurement of 13C/12C and 18O/16O ratios in CO2, 15N/14N ratios in N2O, and 13C/12C and 2H

  13. Zircon U-Pb ages, Hf-O isotopes and trace elements of Mesozoic high Sr/Y porphyries from Ningzhen, eastern China: Constraints on their petrogenesis, tectonic implications and Cu mineralization (United States)

    Wang, Fangyue; Liu, Sheng-Ao; Li, Shuguang; Akhtar, Shamim; He, Yongsheng


    The relationship between high Sr/Y (adakitic) rocks and Cu mineralization has been long recognized but the mechanism remains unclear. The Cretaceous high Sr/Y porphyries in the Ningzhen area host major Cu polymetallic deposits in the Lower Yangtze River Belt (LYRB) of eastern China. These rocks exhibit some geochemical characteristics (e.g., non-radiogenic Pb isotope ratios) that differ from adakitic rocks from adjacent locations in the LYRB. In this study, we present a study of the zircon U-Pb-Hf-O isotope and trace element compositions for five porphyries from Ningzhen to reveal their petrogenesis and how that correlates with Cu-Fe-Mo mineralization. Zircon U-Pb ages of Anjishan (Cu deposit), Tongshan (Cu-Mo deposit) and Xiangshan (Fe deposit) plutons in the Ningzhen area are 108.8 ± 1.5 Ma, 105-107 Ma and 100-105 Ma, respectively, which are significantly younger than the ore-bearing adakites (140 ± 5 Ma) in the western part of the LYRB. Zircon εHf(t) and δ18O values range from - 23.4 to - 10.6 and from 5.7 to 7.0‰, respectively, falling between subduction-related adakites from the other regions in the LYRB and delamination-related adakitic rocks from the adjacent South Tan-Lu Fault Zone. The similarities of Ce4 +/Ce3 + and Eu/Eu* ratios in zircons from Ningzhen and those from the western LYRB indicate higher oxygen fugacity in their magma sources. Ti-in-zircon thermometer yields magma temperatures of 550 to 700 °C (with an average of ~ 650 °C) for the Ningzhen porphyries, which are significantly lower than those of the South Tan-Lu Fault adakites (> 750 °C), but similar to those for the LYRB adakites ( 50), non-radiogenic Pb, enriched Sr-Nd isotopic compositions, negative zircon εHf(t), mantle-like δ18O values, high oxygen fugacities and low magma temperatures. Mafic rocks that co-exist with ore-bearing porphyries or occur as xenoliths in porphyries are widespread. We proposed that the Ningzhen high Sr/Y porphyries originated from mixing of magmas

  14. Evaluating Foraminifera as an Archive for Seawater Chromium Isotopic Composition (United States)

    Wang, X.; Planavsky, N.; Hull, P. M.; Tripati, A.; Reinhard, C.; Zou, H.; Elder, L. E.; Henehan, M. J.


    In recent years there has been growing interest in using chromium isotopes (δ53Cr) as a proxy to investigate the redox evolution of Earth's ocean-atmosphere system throughout geological history. Potential archives for seawater δ53Cr that have been identified to date include iron formations and organic-rich siliciclastic sediments. However, these types of sediments are not common and they are discontinuous over geologic time. As a result, alternative types of archives are needed. Here we evaluate the utility of foraminifera tests as a recorder of seawater δ53Cr. Core-tops used were from different ocean basins. Mono-specific samples of Globigerinoides sacculifer, Orbulina universa, Pulleniatina obliquiloculata, Globoratalia crassula-crassaformis, Globoratalia truncatulinoides, and Globigerinella siphonifera were isolated to investigate inter-species isotope fractionation. Chromium concentrations were measured by isotope dilution method to be 0.1-0.3 μg/g. The δ53Cr values of these species range from 0.2‰ to 2.4‰, with an analytical uncertainty of 0.3‰ (95% confidence). Despite the high analytical uncertainty due to the extremely low levels of Cr present, there is still large detectable variation in foraminiferal δ53Cr values, which overlap presently available seawater values (Bonnand et al., 2013; Scheiderich et al., 2015). Possible explanations for such variations in foraminiferal δ53Cr values include heterogeneity of seawater δ53Cr in the modern oceans, and/or photobiochemical redox cycling of Cr in the surface oceans. Therefore, care should be taken when using foraminifera to reconstruct past seawater δ53Cr values. ReferencesBonnand, P., James, R., Parkinson, I., Connelly, D., Fairchild, I., 2013. The chromium isotopic composition of seawater and marine carbonates. Earth and Planetary Science Letters, 382: 10-20. Scheiderich, K., Amini, M., Holmden, C., Francois, R., 2015. Global variability of chromium isotopes in seawater demonstrated by Pacific

  15. Melt evolution beneath a rifted craton edge: 40Ar/39Ar geochronology and Sr-Nd-Hf-Pb isotope systematics of primitive alkaline basalts and lamprophyres from the SW Baltic Shield (United States)

    Tappe, Sebastian; Smart, Katie A.; Stracke, Andreas; Romer, Rolf L.; Prelević, Dejan; van den Bogaard, Paul


    A new high-precision 40Ar/39Ar anorthoclase feldspar age of 176.7 ± 0.5 Ma (2-sigma) reveals that small-volume alkaline basaltic magmatism occurred at the rifted SW margin of the Baltic Shield in Scania (southern Sweden), at a time of global plate reorganization associated with the inception of Pangea supercontinent break-up. Our combined elemental and Sr-Nd-Hf-Pb isotope dataset for representative basanite and nephelinite samples (>8 wt.% MgO) from 16 subvolcanic necks of the 30 by 40 km large Jurassic volcanic field suggests magma derivation from a moderately depleted mantle source (87Sr/86Sri = 0.7034-0.7048; εNdi = +4.4 to +5.2; εHfi = +4.7 to +8.1; 206Pb/204Pbi = 18.8-19.5). The mafic alkaline melts segregated from mixed peridotite-pyroxenite mantle with a potential temperature of ∼1400 °C at 2.7-4.2 GPa (∼90-120 km depths), which places ultimate melt generation within the convecting upper mantle, provided that the lithosphere-asthenosphere boundary beneath the southern Baltic Shield margin was at ⩽100 km depth during Mesozoic-Cenozoic rifting. Isotopic shifts and incompatible element enrichment relative to Depleted Mantle reflect involvement of at least 20% recycled oceanic lithosphere component (i.e., pyroxenite) with some minor continent-derived sediment during partial melting of well-stirred convecting upper mantle peridotite. Although pargasitic amphibole-rich metasomatized lithospheric mantle is excluded as the main source of the Jurassic magmas from Scania, hydrous ultramafic veins (i.e., hornblendite) may have caused subtle modifications to the compositions of passing sublithospheric melts. For example, modeling suggests that the more radiogenic Hf (εHfi = +6.3 to +8.1) and Pb (206Pb/204Pbi = 18.9-19.5) isotopic compositions of the more sodic and H2O-rich nephelinites, compared with relatively homogenous basanites (εHfi = +4.7 to +6.1; 206Pb/204Pbi = 18.8-18.9), originate from minor interactions between rising asthenospheric melts and

  16. Hafnium isotope results from mid-ocean ridges and Kerguelen. (United States)

    Patchett, P.J.


    176Hf/177Hf ratios are presented for oceanic volcanic rocks representing both extremes of the range of mantle Hf-Nd-Sr isotopic variation. Hf from critical mid-ocean ridge basalts shows that 176Hf/177Hf does indeed have a greater variability than 143Nd/144Nd and 87Sr/86Sr in the depleted mantle. This extra variation is essentially of a random nature, and can perhaps be understood in terms of known Rb/Sr-Sm/Nd-Lu/Hf fractionation relationships. At the other extreme of mantle isotopic compositions, 176Hf/177Hf ratios for igneous rocks from the Indian Ocean island of Kerguelen show a closely similar variation to published 143Nd/144Nd ratios for the same samples. Comparison of Hf-Nd-Sr isotopic relatonships for Tristan da Cunha, Kerguelen and Samoa reveals divergences in the mantle array for ocean-island magma sources, and perhaps suggests that these irregularities are largely the result of an extra component of 87Sr/86Sr variation.-G.R.

  17. Isotopic composition of the ice cores obtained on the Western Plateau of the Mt Elbrus

    Directory of Open Access Journals (Sweden)

    A. V. Kozachek


    Full Text Available The results of the isotopic investigations of several ice cores obtained at the Western Plateau of Mt. Elbrus (the Caucasus are presented. There is a distinct seasonal cycle in the isotopic composition record in these cores. Mean annual and seasonal values of the isotopic composition and accumulation rate were reconstructed for 89 years (1924–2012. These values were compared with the available regional meteorological data and the atmospheric circulation characteristics. It was shown that in the summer season the isotopic composition reflects the local temperature while in winter it depends on the atmospheric circulation.

  18. PVC/HfA/MMA/nano-Al(OH)3复合材料性能的研究%Study on Properties of PVC/HfA/MMA/nano-Al(OH)3 Composite Materials

    Institute of Scientific and Technical Information of China (English)

    王金明; 刘文飞; 张勇; 白庆华


    采用丙烯酸六氟丁酯(HfA)和甲基丙烯酸甲酯(MMA)在纳米Al(OH)3(nano-Al(OH)3)颗粒进行表面聚合,使nano-Al(OH)3表面成亲油性,从而与聚氯乙烯(PVC)颗粒的相容性得到提高。在PVC聚合后期加入这种改性剂,纳米粒子包覆在PVC颗粒表面,改性PVC的综合性能得到改善。最佳试验反应条件为:HfA/MMA/nano-Al(OH)3的配比为3∶5∶92,PVC聚合后期加入占改性PVC树脂含量8%的HfA/MMA/nano-Al(OH)3复合材料,制备出的改性PVC树脂混合料的力学性能和耐热抑烟性能均比空白样品大幅提高。%A new kind of composite materials was prepared by polymerization of butyl acrylate hexafluo- ropropylene (HfA) and methyl methacrylate (MMA) on surface of nano-Al (OH)3 particles. The new composite has very good lipophilicity and improved compatibility with polyvinyl chloride (PVC), By adding the new composite as PVC modifier during polymerization , the nano-composite particles can coat on the surface of PVC particles and the overall propeities of the modified PVC can be improved. The optimal preparation conditions for the new composite were obtained as HfA/MMA/nano-Al (OH)3 equal to 3:5:92,.When the adding amount of the new composite in PVC account for 8% of the PVC resin, the mechanical properties and heatresistance as well as smoke suppression properity of the modified PVC materials are highly improved.

  19. Computational-Experimental Processing of Boride/Carbide Composites by Reactive Infusion of Hf Alloy Melts into B4C (United States)


    elements from the Hf family (i.e., Hf, Ti and Zr ) into a capillary to understand the effects of surface tension and viscosity during processing of melts...project primarily investigated computationally the infusion of liquid elements from the Hf family (i.e., Hf, Ti and Zr ) into a capillary to understand the... effects of surface tension and viscosity during processing of melts with a packed bed of B4C to form boride-carbide precipitates. Although the

  20. Osmium Isotopic Composition of the Sumbar Cretaceous- Tertiary Boundary, Turkmenia (United States)

    Meisel, T.; Krahenbuhl, U.; Nazarov, M. A.


    Turekian (1982) propagated the use of the osmium isotopic composition as a cosmic indicator for the origin of the high osmium (and iridium) layers at the K/T boundaries. He did not consider the osmium isotopic signature of the terrestrial mantle, which also has a chondritic evolution of the Re-Os system. Osmium cannot serve alone as an infallible indicator of the impact theory, but interesting results can be obtained from their investigation. Different K/T boundary section have been analyzed so far for ^187Os/^186Os. An overview of the values is presented in the table. Boundary Clay layer Os ratio Reference Stevns Klint fish clay 1.66 Luck and Turekian, 1983 Woodside Creek 1.12 Lichte et al., 1986 Raton Basin 1.23 Kraehenbuehl et al., 1988 Raton Basin (several) 1.15-1.23 Esser and Turekian, 1989 Sumbar (0-1 cm) 1.16 This work We obtained a complete marine section of the K/T boundary in southern Turkmenia (decribed by Alekseyev, 1988). It shows a very high Ir concentration (66 ppb) at the boundary layer and a remarkable Ir enrichment over crustal rocks continuing up to 30 cm above the boundary. Our aim of this investigation is to analyze several samples from above and below the boundary for the ^187Os/^186Os ratio to obtain a complete picture of the isotopic evolution of the section. We want to evaluate mixing of Os with chondritic ratios with Os from upper crustal rocks. Another goal is to investigate a mobilization of Os. So far only one sample has been analyzed with NTI-MS after fire assay digestion of the sample. The sample 0 to 1 cm has an ^187Os/^186Os ratio of 1.162 +- 13, which is quite low. We expect an even lower value for the boundary clay (0 cm) itself not taking into account a contribution of radiogenic osmium from the decay of terrestrial rhenium. This might put this K/T boundary section closest of all to the present day chondritic value (approx. 1.05). Further analysis will be presented at the meeting. References Alekseyev A. S., Nazarov M. A

  1. Triple sulfur isotope composition of Late Archean seawater sulfate (United States)

    Paris, G.; Fischer, W. W.; Sessions, A. L.; Adkins, J. F.


    Multiple sulfur isotope ratios in Archean sedimentary rocks have provided powerful insights into the behavior of the ancient sulfur cycle, the redox state of fluid Earth, and the timing of the rise of atmospheric oxygen [1]. Most processes fractionate sulfur isotopes in proportion to their mass differences, but the Archean sulfur isotope record is marked by pronounced mass-independent fractionation (MIF, Δ33S≠0). The origin of these signatures has been traditionally interpreted as the result of photolysis of SO2 from short wavelength UV light, with positive Δ33S values recorded in pyrite and negative Δ33S values in sulfate-bearing phases [2]. This long-held hypothesis rests on observations of negative Δ33S from enigmatic barite occurrences from mixed volcanic sedimentary strata in Mesoarchean greenstone terrains. Despite forming the framework for understanding Archean sulfur cycle processes [3], it is largely untested [3]. It is largely untested. Consequently, the biggest challenge to our current understanding of the early sulfur cycle is a poor understanding of the isotopic composition of seawater sulfate. Sulfate evaporite minerals are absent from Archean strata and the sulfur isotope record is written entirely by measurements of pyrite. Carbonate associated sulfate (CAS) provides an important archive for assaying the isotopic composition of ancient seawater sulfate It has been exploited in many studies of Phanerozoic and Proterozoic sulfate but have been only marginally used thus far for Archean samples because of the extremely low concentration of CAS in limestones and dolomites from this era. We have developed a novel MC-ICP-MS approach to solve this problem [4]. This new method lowers the detection limit by up to three orders of magnitude for δ34S and Δ33S measurements, enabling to work on a few nmols of sulfate which represent only tens of mg of sample powders micromilled from specific carbonate textures. Two stratigraphic sections from the 2

  2. Isotopic composition of sulfate accumulations, Northern Calcareous Alps, Austria (United States)

    Bojar, Ana-Voica; Halas, Stanislaw; Bojar, Hans-Peter; Trembaczowski, Andrzej


    The Eastern Alps are characterised by the presence of three main tectonic units, such as the Lower, Middle and Upper Austroalpine, which overlie the Penninicum (Tollmann, 1977). The Upper Austroalpine unit consists of the Northern Calcareous Alps (NCA) overlying the Greywacke zone and corresponding to the Graz Paleozoic, Murau Paleozoic and the Gurktal Nappe. Evaporitic rocks are lacking in the later ones. The Northern Calcareous Alps are a detached fold and thrust belt. The sedimentation started in the Late Carboniferous or Early Permian, the age of the youngest sediments being Eocene. The NCA are divided into the Bajuvaric, Tirolic and Juvavic nappe complexes. The evaporitic Haselgebirge Formation occurs in connection with the Juvavic nappe complex at the base of the Tirolic units (Leitner et al., 2013). The Haselgebirge Formation consists mainly of salt, shales, gypsum and anhydrite and includes the oldest sediments of the NCA. The age of the Haselgebirge Formation, established by using spors and geochronological data, is Permian to Lower Triassic. For the Northern Calcareous Alps, the mineralogy of sulphate accumulations consists mainly of gypsum and anhydrite and subordonates of carbonates. The carbonates as magnesite, dolomite and calcite can be found either as singular crystals or as small accumulations within the hosting gypsum. Sulfides (sphalerite, galena, pyrite), sulfarsenides (enargite, baumhauerite) and native sulphur enrichments are known from several deposits (Kirchner, 1987; Postl, 1990). The investigated samples were selected from various gypsum and halite rich deposits of the Northern Calcareous Alps. A total of over 20 samples were investigated, and both oxygen and sulfur isotopic composition were determined for anhydrite, gyps, polyhalite, blödite and langbeinite. The sulfur isotopic values vary between 10.1 to 14 ‰ (CDT), with three values higher than 14 ‰. The Oxygen isotopic values show a range from 9 to 23 ‰ (SMOW). The sulfur

  3. Oxygen Isotopic Composition of Carbon Dioxide in the Middle Atmosphere (United States)

    Liang, M.; Blake, G. A.; Lewis, B. R.; Yung, Y. L.


    The isotopic composition of long-lived trace gases provides a window into atmospheric transport and chemistry. Carbon dioxide is a particularly powerful tracer, because its abundance remains >100 ppmv in the mesosphere. Current models consider O3 as the main source of O(1D) in the mesosphere, but we note that the photolysis of 16O17O and 16O18O by solar Lyman-α radiation yields O(1D) 10-100 times more enriched in 17O and 18O than that from ozone photodissociation. We therefore incorporate both photochemical sources into stratospheric and mesospheric chemical transport models that quantitatively predict the unusual enhancement of 17O in CO2 from the middle atmosphere. New laboratory and atmospheric measurements are proposed to test our model and validate the use of CO2 isotopic fractionation as a tracer of atmospheric chemical and dynamical processes. Once fully understood the `anomalous' oxygen signature in CO2 can be used in turn to study biogeochemical cycles, in particular to constrain the gross carbon fluxes between the atmosphere and terrestrial biosphere.

  4. Volatile Concentrations and H-Isotope Composition of Unequilibrated Eucrites (United States)

    Sarafian, Adam R.; Nielsen, Sune G.; Marschall, Horst R.; Gaetani, Glenn A.; Hauri, Erik H.; Righter, Kevin; Berger, Eve L.


    Eucrites are among the oldest and best studied asteroidal basalts (1). They represent magmatism that occurred on their parent asteroid, likely 4-Vesta, starting at 4563 Ma and continuing for approx. 30 Myr. Two hypotheses are debated for the genesis of eucrites, a magma ocean model (2), and a mantle partial melting model. In general, volatiles (H, C, F, Cl) have been ignored for eucrites and 4-Vesta, but solubility of wt% levels of H2O are possible at Vestan interior PT conditions. Targeted measurements on samples could aid our understanding considerably. Recent studies have found evidence of volatile elements in eucrites, but quantifying the abundance of volatiles remains problematic (6). Volatile elements have a disproportionately large effect on melt properties and phase stability, relative to their low abundance. The source of volatile elements can be elucidated by examining the hydrogen isotope ratio (D/H), as different H reservoirs have drastically different H isotope compositions. Recent studies of apatite in eucrites have shown that the D/H of 4-Vesta matches that of Earth and carbonaceous chondrites, however, the D/H of apatites may not represent the D/H of a primitive 4-Vesta melt due to the possibility of degassing prior to the crystallization of apatite. Therefore, the D/H of early crystallizing phases must be measured to determine if the D/H of 4-Vesta is equal to that of the Earth and carbonaceous chondrites.

  5. An autochthonous Avalonian basement source for the latest Ordovician Brenton Pluton in the Meguma terrane of Nova Scotia: U-Pb-Hf isotopic constraints and paleogeographic implications (United States)

    Duncan Keppie, J.; Gregory Shellnutt, J.; Dostal, Jaroslav; Fraser Keppie, D.


    The Ediacaran-Ordovician Meguma Supergroup was thrust over Avalonia basement prior to the intrusion of post-Acadian, ca. 370 Ma, S-type granitic batholiths. This has led to two main hypotheses regarding the original location of the Meguma terrane, a continental rise prism bordering either NW Africa or Avalonia. On the other hand, the pre-Acadian, ca. 440 Ma Brenton pluton has yielded the following U/Pb LA-ICP-MS zircon data: (1) 448 ± 3 Ma population peak inferred to be the intrusive age and (2) ca. 550 and 700 Ma inherited ages common to both Avalonia and NW Africa. In contrast, Hf isotopic analyses of zircon yielded model ages ranging from 814 to 1127 Ma with most between 940 and 1040 Ma: such ages are typical of Avalonia and not NW Africa. The ages of the inherited zircons found within the Brenton pluton suggest that it was probably derived by partial melting of sub-Meguma, mid-crustal Avalonian rocks, upon which the Meguma Supergroup was deposited. Although Avalonia is commonly included in the peri-Gondwanan terranes off NW Africa or Amazonia, paleomagnetic data, faunal provinciality, and Hf data suggest that, during the Ediacaran-Early Cambrian, it was an island chain lying near the tropics (ca. 20-30 °S) and was possibly a continuation of the Bolshezemel volcanic arc accreted to northern Baltica during the Ediacaran Timanide orogenesis. This is consistent with the similar derital zircon population in the Ediacaran-Cambrian Meguma Supergroup and the Dividal Group in northeastern Baltica.

  6. Zircon U-Pb ages, Hf isotope data, and tectonic implications of Early-Middle Triassic granitoids in the Ailaoshan high-grade metamorphic belt of Southeast Tibet (United States)

    Wu, Wenbin; Liu, Junlai; Chen, Xiaoyu; Zhang, Lisheng


    The Ailaoshan tectonic belt, where the effects of the Paleo-Tethyan ocean evolution and Indian-Eurasian plate collision are superimposed, is one of the most significant geological discontinuities in western Yunnan province of southeast Tibet. An Ailaoshan micro-block within the belt is bounded by the Ailaoshan suture zone to the west and the Red River Fault to the east, and consists of low- and high-grade metamorphic belts. Late Permian-Middle Triassic granitoids that are widely distributed to the west of the Ailaoshan suture zone and within the Ailaoshan micro-block may yield significant information on the Tethyan tectonic evolution of the Ailaoshan tectonic belt. This study reports new LA-ICP-MS zircon U-Pb geochronology and Hf isotope data of four granitoids from the Ailaoshan high-grade metamorphic belt. Zircon grains from the Yinjie granitoid do not have inherited cores and yield a weighted mean U-Pb age of 247.1 ± 2.0 Ma. The zircon ɛ Hf( t) values range from 7.8 to 12.1, and Hf model ages from 775 to 546 Ma, indicating that the granitoid was derived from juvenile crust. The rims of zircons from the Majie and Yuanjiang granitoids yield weighted mean U-Pb ages of 239.5 ± 1.8 and 237.9 ± 2.6 Ma, respectively, whereas the cores yield ages of 1608-352 Ma. The ɛ Hf( t) values of zircon rims range from -20.4 to -5.3, yielding Hf model ages from 2557 to 1606 Ma and suggesting that the source magma of the Majie and Yuanjiang granitoids was derived from ancient crust. An additional granitoid located near the Majie Village yields a zircon U-Pb age of 241.2 ± 1.0 Ma. Based on our geochronological and geochemical data, combined with geological observations, we propose that the Ailaoshan micro-block was derived from the western margin of the Yangtze block, and is comparable to the Zhongzan and Nam Co micro-blocks. The presence of late Permian mafic rocks with rift-related geochemical characteristics within the Ailaoshan micro-block, together with granitoids derived

  7. Zircon U-Pb ages, Hf isotope data, and tectonic implications of Early-Middle Triassic granitoids in the Ailaoshan high-grade metamorphic belt of Southeast Tibet (United States)

    Wu, Wenbin; Liu, Junlai; Chen, Xiaoyu; Zhang, Lisheng


    The Ailaoshan tectonic belt, where the effects of the Paleo-Tethyan ocean evolution and Indian-Eurasian plate collision are superimposed, is one of the most significant geological discontinuities in western Yunnan province of southeast Tibet. An Ailaoshan micro-block within the belt is bounded by the Ailaoshan suture zone to the west and the Red River Fault to the east, and consists of low- and high-grade metamorphic belts. Late Permian-Middle Triassic granitoids that are widely distributed to the west of the Ailaoshan suture zone and within the Ailaoshan micro-block may yield significant information on the Tethyan tectonic evolution of the Ailaoshan tectonic belt. This study reports new LA-ICP-MS zircon U-Pb geochronology and Hf isotope data of four granitoids from the Ailaoshan high-grade metamorphic belt. Zircon grains from the Yinjie granitoid do not have inherited cores and yield a weighted mean U-Pb age of 247.1 ± 2.0 Ma. The zircon ɛ Hf(t) values range from 7.8 to 12.1, and Hf model ages from 775 to 546 Ma, indicating that the granitoid was derived from juvenile crust. The rims of zircons from the Majie and Yuanjiang granitoids yield weighted mean U-Pb ages of 239.5 ± 1.8 and 237.9 ± 2.6 Ma, respectively, whereas the cores yield ages of 1608-352 Ma. The ɛ Hf(t) values of zircon rims range from -20.4 to -5.3, yielding Hf model ages from 2557 to 1606 Ma and suggesting that the source magma of the Majie and Yuanjiang granitoids was derived from ancient crust. An additional granitoid located near the Majie Village yields a zircon U-Pb age of 241.2 ± 1.0 Ma. Based on our geochronological and geochemical data, combined with geological observations, we propose that the Ailaoshan micro-block was derived from the western margin of the Yangtze block, and is comparable to the Zhongzan and Nam Co micro-blocks. The presence of late Permian mafic rocks with rift-related geochemical characteristics within the Ailaoshan micro-block, together with granitoids derived

  8. Nitrate isotopic composition and ancillary variables (land use, redox, excess N2, age, water isotopics) in California groundwater (United States)

    Veale, Nathan; Moran, Jean; Visser, Ate; Singleton, Michael; Esser, Bradley


    Nitrate is a critical water quality issue in California, the United States and the world. Lawrence Livermore National Laboratory (LLNL) has compiled a large, unique database of California groundwater nitrate isotopic compositions (δ15N-NO3 and δ18O-NO3), acquired largely through more than a decade of coordination with the State of California Groundwater Ambient Monitoring and Assessment (GAMA) program. The water samples are predominantly from shallow aquifers accessed by domestic and monitoring wells. The database of >1,300 nitrate isotopic compositions includes a number of important ancillary parameters: DO, ORP and DOC (measured for 18% of samples); excess air and dissolved N2 (24%); water isotopic composition (δ18O-H2O and δD-H2O) (43%); and tritium/3He groundwater age (27%). Methods used at LLNL include sample preparation by the denitrifier method (for δ15N-NO3 and δ18O-NO3) and Isotope Ratio Mass Spectrometry with (δ15N-NO3 and δ18O-NO3 and δ18O-H2O and δD-H2O), Noble Gas Mass Spectrometry (NGMS; for excess air and groundwater age), and Membrane Inlet Mass Spectrometry (MIMS; for major dissolved gases and excess N2). Redox indicators (DO, ORP and DOC) in conjunction with excess N2, groundwater age, and nitrate isotopic composition are used to assess the presence or absence, and potentially the rate of, saturated-zone denitrification. Comparison of δ18O-NO3 to δ18O-H2O isotopic composition is used to distinguish synthetic nitrate from nitrification of reduced forms of nitrogen as a source of groundwater nitrate. Groundwater age is used to discern timing and temporal trends in groundwater nitrate isotopic composition. The relationship of nitrate isotopic composition to ancillary parameters (redox, excess N2, water isotopic composition and groundwater age) is explored, along with its relationship to well location, screened interval, and land use, with a focus on the extent of saturated-zone denitrification and the significance of synthetic nitrate as

  9. Zircon U-Pb and Lu-Hf isotope study of the Neoproterozoic Haizhou Group in the Sulu orogen: Provenance and tectonic implications (United States)

    Zhou, Jian-Bo; Wilde, Simon A.; Liu, Fu-Lai; Han, Jie


    The Neoproterozoic Haizhou Group crops out sporadically in the Sulu orogen in east-central China. It is divided into the Jinping and Yuntai formations and consists of quartzite, quartz schist, marble and graphite- and apatite-bearing sequences. Major and trace element data for quartz schist from the two formations indicate that these rocks have a greywacke protolith and have been deposited during strong tectonic activity. LA-ICPMS U-Pb dating of detrital zircon yields ages of 635 to 1074 Ma for three samples from the Jinping Formation and 611 to 943 Ma for two samples from the Yuntai Formation. More than 78% of the detrital zircons from the two formations have U-Pb ages grouped between 700 and 890 Ma, with two clusters peaking at 758 Ma and 828 Ma, respectively. This indicates that their provenance is magmatic rocks of Neoproterozoic age that have a tectonic affinity to the South China Block (SCB). A few older zircon populations with peak U-Pb ages at 943 and 1074 Ma are also present. A younger population shows peaks at 661 and 611 Ma. This suggests that deposition of the Haizhou Group was later than ~ 611 Ma rather than during the Mesoproterozoic as previously thought. Zircon Lu-Hf isotope data collected from the same U-Pb sites show negative ɛHf(t) values of - 22.8 to - 7.4 and Hf model ages of 2341 to 3100 Ma. This indicates that the Neoproterozoic magmatic rocks were derived from reworking of ancient Paleoproterozoic to Archean crust. The results support the contention that the Haizhou Group is similar to the Wulian Group at the northwestern edge of the Sulu orogen, both having a SCB affinity, but that the Penglai Group does not belong to the SCB because of the absence of Neoproterozoic ages. This lends support to the conclusion that the Triassic suture between the North China and South China blocks is located along the Baichihe-Yantai Fault, which lies north of the Wulian Complex and south of the Jiaobei Terrane; thus the Wulian-Yantai Fault is not the suture

  10. Stable isotope composition of atmospheric carbon monoxide. A modelling study

    Energy Technology Data Exchange (ETDEWEB)

    Gromov, Sergey S.


    This study aims at an improved understanding of the stable carbon and oxygen isotope composition of the carbon monoxide (CO) in the global atmosphere by means of numerical simulations. At first, a new kinetic chemistry tagging technique for the most complete parameterisation of isotope effects has been introduced into the Modular Earth Submodel System (MESSy) framework. Incorporated into the ECHAM/MESSy Atmospheric Chemistry (EMAC) general circulation model, an explicit treatment of the isotope effects on the global scale is now possible. The expanded model system has been applied to simulate the chemical system containing up to five isotopologues of all carbon- and oxygen-bearing species, which ultimately determine the δ{sup 13}C, δ{sup 18}O and Δ{sup 17}O isotopic signatures of atmospheric CO. As model input, a new stable isotope-inclusive emission inventory for the relevant trace gases has been compiled. The uncertainties of the emission estimates and of the resulting simulated mixing and isotope ratios have been analysed. The simulated CO mixing and stable isotope ratios have been compared to in-situ measurements from ground-based observatories and from the civil-aircraft-mounted CARIBIC-1 measurement platform. The systematically underestimated {sup 13}CO/{sup 12}CO ratios of earlier, simplified modelling studies can now be partly explained. The EMAC simulations do not support the inferences of those studies, which suggest for CO a reduced input of the highly depleted in {sup 13}C methane oxidation source. In particular, a high average yield of 0.94 CO per reacted methane (CH{sub 4}) molecule is simulated in the troposphere, to a large extent due to the competition between the deposition and convective transport processes affecting the CH{sub 4} to CO reaction chain intermediates. None of the other factors, assumed or disregarded in previous studies, however hypothesised to have the potential in enriching tropospheric CO in {sup 13}C, were found significant

  11. Rhyolite magma evolution recorded in isotope and trace element composition of zircon from Halle Volcanic Complex (United States)

    Słodczyk, E.; Pietranik, A.; Breitkreuz, C.; Fanning, C. M.; Anczkiewicz, R.; Ehling, B.-C.


    Voluminous felsic volcanic magmas were formed in Central Europe at the Carboniferous/Permian boundary in numerous pull-apart basins; one of which is the Saale Basin, which holds the Halle Volcanic Complex (HVC), the focus of this study. The rhyolites in the HVC formed laccoliths and scarce lavas, and occur in two different textural types: fine and coarse porphyritic. Zircon isotope and trace element composition was analysed in four units, two per each textural type. Zircon from the different units shows similar ranges in εHf (- 4.1 to - 8.1) and δ18O values (6.51-8.26), indicating similar sources and evolution processes for texturally diverse rhyolites from the HVC. Scarce inherited zircon ranges from ~ 315 Ma to ~ 2100 Ma with the major groupings around 315-550 Ma. These ages are typical for Devonian arc magmatic activity (350-400 Ma) and Cadomian igneous rocks (500-600 Ma), which occur in the basement presently underlying the HVC. Therefore, the source of the rhyolites was multicomponent and probably represented by a basement composed of various crystalline rocks. Trace elements in zircon show similar distributions in all analysed samples, which is broadly consistent with zircon cores crystallizing in a less evolved magma undergoing limited fractional crystallization, whilst the zircon rims crystallized from a magma undergoing extensive fractional crystallization of major and accessory minerals. Interestingly, comparison of the zircon composition in HVC rhyolites and other rhyolites worldwide shows that the observed trends are similar in such rhyolites despite the values being different. This may suggest that most of the zircon in rhyolites crystallizes at a similar stage in the rhyolite magma evolution, from magmas undergoing extensive crystallization of major phases and apatite. The implication is that most of the zircon represents late stage crystallization, but also that antecrystic component may be present and preserve information on the development of

  12. Geological, geochronological, geochemical, and Sr-Nd-O-Hf isotopic constraints on origins of intrusions associated with the Baishan porphyry Mo deposit in eastern Tianshan, NW China (United States)

    Wang, Yinhong; Xue, Chunji; Liu, Jiajun; Zhang, Fangfang


    The Baishan porphyry Mo deposit (0.72 Mt; 0.06 % Mo) is located in the interior of the eastern Tianshan orogenic belt in Xinjiang, NW China. The deposit comprises 15 orebodies that are associated with monzogranite and granite porphyry stocks and are structurally controlled by roughly EW-trending faults. Secondary ion mass spectrometry (SIMS) zircon U-Pb dating of the monzogranite and granite porphyry yielded the Middle Triassic age (228 ± 2 to 227 ± 2 Ma), which coincide with the molybdenite Re-Os model ages ranging from 226 ± 3 to 228 ± 3 Ma. The Triassic monzogranite and granite porphyry belong to high-K calc-alkaline series and are characterized by high SiO2 and Al2O3 and low MgO, TiO2, and P2O5 concentrations, with negative Eu anomalies (δEu = 0.55-0.91). The least-altered monzogranite and granite porphyry yield uniform ɛ Nd( t) values from +1.6 to +3.6, and wide (87Sr/86Sr) i ratios ranging between 0.7035 and 0.7071, indicating that they were derived from the lower crust. In situ O-Hf isotopic analyses on zircon using SIMS and laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) indicate that the δ18O and ɛ Hf( t) values of zircon from a monzogranite sample vary from 6.1 to 7.3 ‰ and +8.0 to +11.7, respectively, whereas zircon from a granite porphyry sample vary from 6.2 to 6.9 ‰ and +7.3 to +11.2, respectively. The geochemical and isotopic data imply that the primary magmas of the Baishan granite were likely derived from partial melts from the lower crust involving some mantle components. The Baishan Mo deposit and granitic emplacement were proposed to be most likely related to post-orogenic lithospheric extension and magmatic underplating. An extensional event coupled with the rising of hot mantle-derived melts triggered partial melting of the lower crust, as well as provided metals (Mo).

  13. Tooth enamel maturation reequilibrates oxygen isotope compositions and supports simple sampling methods (United States)

    Trayler, Robin B.; Kohn, Matthew J.


    Oxygen isotope and major element zoning patterns of several disparate ungulate teeth were collected to evaluate the timing and geometry of enamel formation, records of isotope zoning, and tooth enamel sampling strategies. Isotopic zoning in mammalian tooth enamel encodes a sub-annual time series of isotopic variation of an animal's body water composition, with a damping factor that depends on the specifics of how enamel mineralizes. Enamel formation comprises two stages: precipitation of appositional enamel with a high CO3:PO4 ratio, followed by precipitation of maturational enamel with a lower CO3:PO4. If appositional and maturational enamel both contribute to isotope compositions (but with different CO3:PO4), and if isotope compositions vary seasonally, paired δ18O values from CO3 and PO4 profiles should show a spatial separation. CO3 isotope patterns should be shifted earlier seasonally than PO4 isotope patterns. Such paired profiles for new and published data show no resolvable shifts, i.e. CO3 and PO4 δ18O profiles show coincident maxima and minima. This coincidence suggests that enamel maturation reequilibrates appositional isotope compositions. If enamel maturation establishes enamel isotope compositions, the geometry of maturation, not apposition, should be considered when devising sampling protocols. X-ray maps of Ca zoning show that the majority of enamel (inner and middle layers) mineralizes heavily at a high angle to the external tooth surface and the enamel-dentine junction over length scales of 2-4 mm, while the outer enamel surface mineralizes more slowly. These data suggest that isotopic sampling strategies should parallel maturational geometry and focus on interior enamel to improve data fidelity. The magnitude of isotopic damping is also smaller than implied in previous studies, so tooth enamel zoning more closely reflects original body water isotopic variations than previously assumed.

  14. Isotopic and Elemental Composition of Roasted Coffee as a Guide to Authenticity and Origin. (United States)

    Carter, James F; Yates, Hans S A; Tinggi, Ujang


    This study presents the stable isotopic and elemental compositions of single-origin, roasted coffees available to retail consumers. The δ(13)C, δ(15)N, and δ(18)O compositions were in agreement with those previously reported for green coffee beans. The δ(15)N composition was seen to be related to organic cultivation, reflected in both δ(2)H and δ(18)O compositions. The δ(13)C composition of extracted caffeine differed little from that of the bulk coffee. Stepwise discriminant analysis with jackknife tests, using isotopic and elemental data, provided up to 77% correct classification of regions of production. Samples from Africa and India were readily classified. The wide range in both isotopic and elemental compositions of samples from other regions, specifically Central/South America, resulted in poor discrimination between or within these regions. Simpler X-Y and geo-spatial plots of the isotopic data provided effective visual means to distinguish between coffees from different regions.

  15. Light element isotopic compositions of cometary matter returned by the STARDUST mission

    Energy Technology Data Exchange (ETDEWEB)

    McKeegan, K D; Aleon, J; Bradley, J; Brownlee, D; Busemann, H; Butterworth, A; Chaussidon, M; Fallon, S; Floss, C; Gilmour, J; Gounelle, M; Graham, G; Guan, Y; Heck, P R; Hoppe, P; Hutcheon, I D; Huth, J; Ishii, H; Ito, M; Jacobsen, S B; Kearsley, A; Leshin, L A; Liu, M; Lyon, I; Marhas, K; Marty, B; Matrajt, G; Meibom, A; Messenger, S; Mostefaoui, S; Nakamura-Messenger, K; Nittler, L; Palma, R; Pepin, R O; Papanastassiou, D A; Robert, F; Schlutter, D; Snead, C J; Stadermann, F J; Stroud, R; Tsou, P; Westphal, A; Young, E D; Ziegler, K; Zimmermann, L; Zinner, E


    Hydrogen, carbon, nitrogen, and oxygen isotopic compositions are heterogeneous among comet 81P/Wild2 particle fragments, however extreme isotopic anomalies are rare, indicating that the comet is not a pristine aggregate of presolar materials. Non-terrestrial nitrogen and neon isotope ratios suggest that indigenous organic matter and highly volatile materials were successfully collected. Except for a single circumstellar stardust grain, silicate and oxide minerals have oxygen isotopic compositions consistent with solar system origin. One refractory grain is {sup 16}O-enriched like refractory inclusions in meteorites, suggesting formation in the hot inner solar nebula and large-scale radial transport prior to comet accretion in the outer solar system.

  16. The pre-Atlantic Hf isotope evolution of the east Laurentian continental margin: Insights from zircon in basement rocks and glacial tillites from northern New Jersey and southeastern New York (United States)

    Zirakparvar, N. Alex; Setera, Jacob; Mathez, Edmond; Vantongeren, Jill; Fossum, Ryanna


    This paper presents laser ablation U-Pb age and Hf isotope data for zircons from basement rocks and glacial deposits in northern New Jersey and southeastern New York. The purpose is to understand the eastern Laurentian continental margin's Hf isotope record in relation to its geologic evolution prior to the opening of the Atlantic Ocean. The basement samples encompass a Meso- to Neoproterozoic continental margin arc, an anatectic magmatic suite, as well as a Late Ordovician alkaline igneous suite emplaced during post-orogenic melting of the lithospheric mantle. Additional samples were collected from terminal moraines of two Quaternary continental ice sheets. Across the entire dataset, zircons with ages corresponding to the timing of continental margin arc magmatism ( 1.4 Ga to 1.2 Ga) have positive εHf(initial) values that define the more radiogenic end of a crustal evolution array. This array progresses towards more unradiogenic εHf(initial) values along a series of low 176Lu/177Hf (0.022 to 0.005) trajectories during subsequent anatectic magmatism ( 1.2 Ga to 1.0 Ga) and later metamorphic and metasomatic re-working ( 1.0 Ga to 0.8 Ga) of the continental margin arc crust. In contrast, nearly chondritic εHf(initial) values from the Late Ordovician alkaline magmas indicate that the Laurentian margin was underlain by a re-fertilized mantle source. Such a source may have developed by subduction enrichment of the mantle wedge beneath the continental margin during the Mesoproterozoic. Additionally, preliminary data from a metasedimentary unit of unknown provenance hints at the possibility that some of the sediments occupying this portion of the Laurentian margin prior to the Ordovician were sourced from crust older than 1.9 Ga.

  17. Modelling and interpreting the isotopic composition of water vapour in convective updrafts

    Directory of Open Access Journals (Sweden)

    M. Bolot


    Full Text Available The isotopic compositions of water vapour and its condensates have long been used as tracers of the global hydrological cycle, but may also be useful for understanding processes within individual convective clouds. We review here the representation of processes that alter water isotopic compositions during processing of air in convective updrafts and present a unified model for water vapour isotopic evolution within undiluted deep convective cores, with a special focus on the out-of-equilibrium conditions of mixed-phase zones where metastable liquid water and ice coexist. We use our model to show that a combination of water isotopologue measurements can constrain critical convective parameters, including degree of supersaturation, supercooled water content and glaciation temperature. Important isotopic processes in updrafts include kinetic effects that are a consequence of diffusive growth or decay of cloud particles within a supersaturated or subsaturated environment; isotopic re-equilibration between vapour and supercooled droplets, which buffers isotopic distillation; and differing mechanisms of glaciation (droplet freezing vs. the Wegener–Bergeron–Findeisen process. As all of these processes are related to updraft strength, particle size distribution and the retention of supercooled water, isotopic measurements can serve as a probe of in-cloud conditions of importance to convective processes. We study the sensitivity of the profile of water vapour isotopic composition to differing model assumptions and show how measurements of isotopic composition at cloud base and cloud top alone may be sufficient to retrieve key cloud parameters.

  18. Detrital zircon U-Pb geochronology, Lu-Hf isotopes and REE geochemistry constrains on the provenance and tectonic setting of Indochina Block in the Paleozoic (United States)

    Wang, Ce; Liang, Xinquan; Foster, David A.; Fu, Jiangang; Jiang, Ying; Dong, Chaoge; Zhou, Yun; Wen, Shunv; Van Quynh, Phan


    In situ U-Pb geochronology, Lu-Hf isotopes and REE geochemical analyses of detrital zircons from Cambrian-Devonian sandstones in the Truong Son Belt, central Vietnam, are used to provide the information of provenance and tectonic evolution of the Indochina Block. The combined detrital zircon age spectra of all of the samples ranges from 3699 Ma to 443 Ma and shows with dominant age peaks at ca. 445 Ma and 964 Ma, along with a number of age populations at 618-532 Ma, 1160-1076 Ma, 1454 Ma, 1728 Ma and 2516 Ma. The zircon age populations are similar to those from time equivalent sedimentary sequences in continental blocks disintegrated from the East Gondwana during the Phanerozoic. The younger zircon grains with age peaks at ca. 445 Ma were apparently derived from middle Ordovician-Silurian igneous and metamorphic rocks in Indochina. Zircons with ages older than about 600 Ma were derived from other Gondwana terrains or recycled from the Precambrian basement of the Indochina Block. Similarities in the detrital zircon U-Pb ages suggest that Paleozoic strata in the Indochina, Yangtze, Cathaysia and Tethyan Himalayas has similar provenance. This is consistent with other geological constrains indicating that the Indochina Block was located close to Tethyan Himalaya, northern margin of the India, and northwestern Australia in Gondwana.

  19. Detrital zircon U-Pb ages and Hf isotopic constraints on the terrigenous sediments of the Western Alps and their paleogeographic implications (United States)

    Chu, Yang; Lin, Wei; Faure, Michel; Wang, Qingchen


    Detrital zircons from Cretaceous micaschist, late Eocene-earliest Oligocene sandstone and early Oligocene siltstone of the Western Alps fall into three main separable age clusters at 610-540 Ma, 490-430 Ma, and 340-280 Ma that correspond to the Cadomian (Neoproterozoic), Ordovician, and Variscan (Carboniferous) events widespread in western and central Europe. Hf isotopic results indicate that these three magmatic and tectonic episodes did not give rise to significant production of juvenile crust. A distinguishable group of Triassic zircons, around 250-200 Ma which is considered to derive from the Southern Alps, has been detected in the early Oligocene "Schistes à Blocs" formation and the Briançonnais "Flysch Noir". In contrast, this age group is absent in late Eocene to earliest Oligocene sandstones. In agreement with sedimentological studies, our results show that the main source areas of the Eocene sandstone were probably located in the European continent. The arrival of detritus from the Internal Zone occurred in early Oligocene, coeval with the tectonic rotation from northwestward to westward in the propagation of allochthonous units. Based on previous studies and our new data, we argue that the Briançonnais Zone was likely a paleorelief since the middle Eocene that accounts for the lack of detritus from the Adriatic units. Contemporary sediments were accumulated in the foredeep of the Adriatic plate. From Oligocene time onward, the blockage was cut through after a regional uplifting, and thus, the Internal Zone started to provide detritus into the western flexural basins.

  20. Controls on the stable isotope compositions of travertine from hyperalkaline springs in Oman: Insights from clumped isotope measurements (United States)

    Falk, E. S.; Guo, W.; Paukert, A. N.; Matter, J. M.; Mervine, E. M.; Kelemen, P. B.


    Carbonate formation at hyperalkaline springs is typical of serpentinization in peridotite massifs worldwide. These travertines have long been known to exhibit large variations in their carbon and oxygen isotope compositions, extending from apparent equilibrium values to highly depleted values. However, the exact causes of these variations are not well constrained. We analyzed a suite of well-characterized fresh carbonate precipitates and travertines associated with hyperalkaline springs in the peridotite section of the Samail ophiolite, Sultanate of Oman, and found their clumped isotope compositions vary systematically with formation environments. Based on these findings, we identified four main processes controlling the stable isotope compositions of these carbonates. These include hydroxylation of CO2, partial isotope equilibration of dissolved inorganic carbon, mixing between isotopically distinct carbonate end-members, and post-depositional recrystallization. Most notably, in fresh crystalline films on the surface of hyperalkaline springs and in some fresh carbonate precipitates from the bottom of hyperalkaline pools, we observed large enrichments in Δ47 (up to ∼0.2‰ above expected equilibrium values) which accompany depletions in δ18O and δ13C, yielding about 0.01‰ increase in Δ47 and 1.1‰ decrease in δ13C for every 1‰ decrease in δ18O, relative to expected equilibrium values. This disequilibrium trend, also reflected in preserved travertines ranging in age from modern to ∼40,000 years old, is interpreted to arise mainly from the isotope effects associated with the hydroxylation of CO2 in high-pH fluids and agrees with our first-order theoretical estimation. In addition, in some fresh carbonate precipitates from the bottom of hyperalkaline pools and in subsamples of one preserved travertine terrace, we observed additional enrichments in Δ47 at intermediate δ13C and δ18O, consistent with mixing between isotopically distinct carbonate end

  1. Seasonality of Oxygen isotope composition in cow (Bos taurus) hair and its model interpretation (United States)

    Chen, Guo; Schnyder, Hans; Auerswald, Karl


    Oxygen isotopes in animal and human tissues are expected to be good recorders of geographical origin and migration histories based on the isotopic relationship between hair oxygen and annual precipitation and the well-known spatial pattern of oxygen isotope composition in meteoric water. However, seasonal variation of oxygen isotope composition may diminish the origin information in the tissues. Here the seasonality of oxygen isotope composition in tail hair was investigated in a domestic suckler cow (Bos taurus) that underwent different ambient conditions, physiological states, and keeping and feeding strategies during five years. A detailed mechanistic model involving in ambient conditions, soil properties and animal physiology was built to explain this variation. The measured oxygen isotope composition in hair was significantly related (pwater in a regression analysis. Modelling suggested that this relation was only partly derived from the direct influence of feed moisture. Ambient conditions (temperature, moisture) did not only influence the isotopic signal of precipitation but also affected the animal itself (drinking water demand, transcutaneous vapor etc.). The clear temporal variation thus resulted from complex interactions with multiple influences. The twofold influence of ambient conditions via the feed and via the animal itself is advantageous for tracing the geographic origin because the oxygen isotope composition is then less influenced by variations in moisture uptake; however, it is unfavorable for indicating the production system, e.g. to distinguish between milk produced from fresh grass or from silage.

  2. An in situ zircon Hf isotopic,U-Pb age and trace element study of banded granulite xenolith from Hannuoba basalt:Tracking the early evolution of the lower crust in the North China craton

    Institute of Scientific and Technical Information of China (English)

    ZHENG Jianping; LU Fengxiang; YU Chunmei; TANG Huayun


    Backscattered electron images, in situ Hf isotopes, U-Pb ages and trace elements of zircons in a banded granulite xenolith from Hannuoba basalt have been studied. The results show that the banded granulite is a sample derived from the early lower crust of the North China craton. It is difficult to explain the petrogenesis of the xenolith with a single process. Abundant information on several processes, however, is contained in the granulite. These processes include the addition of mantle material, crustal remelting, metamorphic differentiation and the delamination of early lower crust. About 80% of zircons studied yield ages of 1842±40 Ma, except few ages of 3097-2824 Ma and 2489-2447 Ma. The zircons with ages older than 2447 Ma have high εHf (up to +18.3) and high Hf model age (2.5-2.6 Ga), indicating that the primitive materials of the granulite were derived mainly from a depleted mantle source in late Archean. Most εHf of the zircons with early Proterozoic U-Pb age vary around zero, but two have high εHf up to +9.2-+10.2, indicating mantle contribution during the collision and assembly between the Eastern and Western blocks in the early Proterozoic that resulted in the amalgamation of the North China craton.

  3. Origin and evolution of the Tengchong block, southeastern margin of the Tibetan Plateau: Zircon U-Pb and Lu-Hf isotopic evidence from the (meta-) sedimentary rocks and intrusions (United States)

    Li, Dapeng; Chen, Yuelong; Hou, Kejun; Luo, Zhaohua


    U-Pb ages and Hf isotopic data from detrital zircons of Gaoligongshan metamorphic complex and the Carboniferous Menghong Group and igneous zircons from intrusions constrain the origin, tectonic affinity (East Gondwana), crustal evolution processes, and the properties of regional high-grade metamorphic rocks in the Tengchong block of southeastern China. Three granites intruded into the Tengchong block at 72 Ma, 114 Ma and 122 Ma. Detrital zircons range in age from Archean to Late Ordovician for both the Carboniferous Menghong Group and the Gaoligongshan metamorphic complex. Analyses for these two units yield similar age clusters at 2.5 Ga, 1.6 Ga, 1.17 Ga, 0.95 Ga, and 0.65-0.5 Ga as well as parallel Hf isotopic distributions. The protolith of the studied Gaoligongshan complex in the Tengchong block should deposit in the Late Paleozoic. Detrital zircon age distribution patterns of the Carboniferous Menghong Group and the Gaoligongshan complex show dominant younger Grenvillian age peaks at 0.95 Ga, indicating the strong paleogeographic connection of the Tengchong block with the Indian margin. The Hf isotopic comparison of both detrital and igneous dated-zircon shows that the Tengchong block can be represented by the post-Archean Indian continental margin. After 250 Ma, the intensive magma events affected the region and considerable juvenile material accreted to the crust of the Tengchong block.

  4. Clumped Isotope Composition of Cold-Water Corals: A Role for Vital Effects? (United States)

    Spooner, P.; Guo, W.; Robinson, L. F.


    Measurements on a set of cold-water corals (mainly Desmophyllum dianthus) have suggested that their clumped isotope composition could serve as a promising proxy for reconstructing paleocean temperatures. Such measurements have also offered support for certain isotope models of coral calcification. However, there are differences in the clumped isotope compositions between warm-water and cold-water corals, suggesting that different kinds of corals could have differences in their biocalcification processes. In order to understand the systematics of clumped isotope variations in cold-water corals more fully, we present clumped isotope data from a range of cold-water coral species from the tropical Atlantic and the Southern Ocean.Our samples were either collected live or recently dead (14C ages biocalcification may not apply equally well to all corals. Clumped isotope vital effects may be present in certain cold-water corals as they are in warm-water corals, complicating the use of this paleoclimate proxy.

  5. Effect of HF concentration on the composition and distribution of Ge species in the framework of ITQ-13 and ITQ-17 zeolites

    KAUST Repository

    Liu, Xiaolong


    Two germanosilicates with zeolitic structures, namely ITQ-13 and ITQ-17, have been synthesized from gels containing various amounts of hydrofluoric acid. Although both zeolites possess similar compositions, they differ not only by their pore size and framework topology but also by the nature of the cavities surrounding fluoride species in the structure. For ITQ-17, in which fluoride is almost exclusively located in D4R units, a decrease in HF concentration in the gel has no influence on the fluoride content in the zeolite. However, it favors the incorporation of germanium species in the framework, particularly in D4R units. Zeolites obtained at low HF concentrations are characterized by high Ge contents and Si/Ge atomic ratios close to 1 in D4R units. In the case of ITQ-13, the possibility for fluoride to reside not only in D4R units but also in the larger [415262] cages minimizes the influence of the HF concentration on the zeolite framework composition. Reducing the HF concentration in the gel has no effect on the Si/Ge ratio in the final zeolite but it decreases the fluoride content in the structure. At low HF concentration, fluoride is absent from [415262] cages and is almost exclusively present in all-silica D4R units. As the concentration increases, fluoride starts to occupy Ge-rich D4R and [415 262] cages, as clearly evidenced by 19F NMR. By contrast to ITQ-17, the amount of HF in the gel does not influence the distribution of Ge species in the framework. © 2012 Published by Elsevier Inc.

  6. Fractionation of Oxygen Isotopes by Thermal Ionization Mass Spectrometry Inferred from Simultaneous Measurement of (17)O/(16)O and (18)O/(16)O Ratios and Implications for the (182)Hf-(182)W Systematics. (United States)

    Trinquier, Anne


    Accurate (182)Hf-(182)W chronology of early planetary differentiation relies on highly precise and accurate tungsten isotope measurements. WO3(-) analysis by negative thermal ionization mass spectrometry requires W(17)O(16)O2(-), W(17)O2(16)O(-), W(18)O(16)O2(-), W(17)O3(-), W(17)O(18)O(16)O(-), and W(18)O2(16)O(-) isotopologue interference corrections on W(16)O3(-) species ( Harper et al. Geochim. Cosmochim. Acta 1996 , 60 , 1131 ; Quitté et al. Geostandard. Newslett. 2002 , 26 , 149 ; Trinquier et al. Anal. Chem. 2016 , 88 , 1542 ; Touboul et al. Nature 2015 , 520 , 530 ; Touboul et al. Int. J. Mass Spectrom. 2012 , 309 , 109 ). In addition, low ion beam intensity counting statistics combined with Faraday cup detection noise limit the precision on the determination of (18)O/(16)O and (17)O/(16)O relative abundances. Mass dependent variability of (18)O/(16)O over the course of an analysis and between different analyses calls for oxide interference correction on a per integration basis, based on the in-run monitoring of the (18)O/(16)O ratio ( Harper et al. Geochim. Cosmochim. Acta 1996 , 60 , 1131 ; Quitté et al. Geostandard. Newslett. 2002 , 26 , 149 ; Trinquier et al. Anal. Chem. 2016 , 88 , 1542 ). Yet, the (17)O/(16)O variation is normally not being monitored and, instead, inferred from the measured (18)O/(16)O variation, assuming a δ(17)O-δ(18)O Terrestrial Fractionation Line ( Trinquier et al. Anal. Chem. 2016 , 88 , 1542 ). The purpose of the present study is to verify the validity of this assumption. Using high resistivity amplifiers, (238)U(17)O2 and (238)U(18)O2 ion beams down to 1.6 fA have been monitored simultaneously with (235,238)U(16)O2 species in a uranium certified reference material. This leads to a characterization of O isotope fractionation by thermal ionization mass spectrometry in variable loading and running conditions (additive-to-sample ratio, PO2 pressure, presence of ionized metal and oxide species). Proper determination of O

  7. Hydrogen and oxygen in brine shrimp chitin reflect environmental water and dietary isotopic composition (United States)

    Nielson, Kristine E.; Bowen, Gabriel J.


    Hydrogen and oxygen isotope ratios of the common structural biopolymer chitin are a potential recorder of ecological and environmental information, but our understanding of the mechanisms of incorporation of H and O from environmental substrates into chitin is limited. We report the results of a set of experiments in which the isotopic compositions of environmental water and diet were varied independently in order to assess the contribution of these variables to the H and O isotopic composition of Artemia franciscana chitin. Hydrogen isotope ratios of chitin were strongly linearly correlated with both food and water, with approximately 26% of the hydrogen signal reflecting food and approximately 38% reflecting water. Oxygen isotopes were also strongly correlated with the isotopic composition of water and food, but whereas 69% of oxygen in chitin exchanged with environmental water, only 10% was derived from food. We propose that these observations reflect the position-specific, partial exchange of H and O atoms with brine shrimp body water during the processes of digestion and chitin biosynthesis. Comparison of culture experiments with a set of natural samples collected from the Great Salt Lake, UT in 2006 shows that, with some exceptions, oxygen isotope compositions of chitin track those of water, whereas hydrogen isotopes vary inversely with those of lake water. The different behavior of the two isotopic systems can be explained in terms of a dietary shift from allochthonous particulate matter with relatively higher δ 2H values in the early spring to autochthonous particulate matter with significantly lower δ 2H values in the late summer to autumn. These results suggest oxygen in chitin may be a valuable proxy for the oxygen isotopic composition of environmental water, whereas hydrogen isotope values from the same molecule may reveal ecological and biogeochemical changes within lakes.

  8. The iron isotope composition of enstatite meteorites: Implications for their origin and the metal/sulfide Fe isotopic fractionation factor (United States)

    Wang, Kun; Savage, Paul S.; Moynier, Frédéric


    Despite their unusual chemical composition, it is often proposed that the enstatite chondrites represent a significant component of Earth’s building materials, based on their terrestrial similarity for numerous isotope systems. In order to investigate a possible genetic relationship between the Fe isotope composition of enstatite chondrites and the Earth, we have analyzed 22 samples from different subgroups of the enstatite meteorites, including EH and EL chondrites, aubrites (main group and Shallowater) and the Happy Canyon impact melt. We have also analyzed the Fe isotopic compositions of separated (magnetic and non-magnetic) phases from both enstatite chondrites and achondrites. On average, EH3-5 chondrites (δ56Fe = 0.003 ± 0.042‰; 2 standard deviation; n = 9; including previous literature data) as well as EL3 chondrites (δ56Fe = 0.030 ± 0.038‰; 2 SD; n = 2) have identical and homogeneous Fe isotopic compositions, indistinguishable from those of the carbonaceous chondrites and average terrestrial peridotite. In contrast, EL6 chondrites display a larger range of isotopic compositions (-0.180‰ < δ56Fe < 0.181‰; n = 11), a result of mixing between isotopically distinct mineral phases (metal, sulfide and silicate). The large Fe isotopic heterogeneity of EL6 is best explained by chemical/mineralogical fragmentation and brecciation during the complex impact history of the EL parent body. Enstatite achondrites (aubrites) also exhibit a relatively large range of Fe isotope compositions: all main group aubrites are enriched in the light Fe isotopes (δ56Fe = -0.170 ± 0.189‰; 2 SD; n = 6), while Shallowater is, isotopically, relatively heavy (δ56Fe = 0.045 ± 0.101‰; 2 SD; n = 4; number of chips). We take this variation to suggest that the main group aubrite parent body formed a discreet heavy Fe isotope-enriched core, whilst the Shallowater meteorite is most likely from a different parent body where core and silicate material remixed. This could be

  9. A continuous flow isotope ratio mass spectrometry method for high precision determination of dissolved gas ratios and isotopic composition

    DEFF Research Database (Denmark)

    Charoenpong, C. N.; Bristow, L. A.; Altabet, M. A.


    Dissolved gas ratios and isotopic compositions provide essential information about the biological and physical mechanisms influencing N-2, O-2, and Ar in aquatic systems. Current methods available are either limited by overall cost, labor-intensive sample collection and analysis, or insufficient ...

  10. Sr-Nd-Hf isotopes of the intrusive rocks in the Cretaceous Xigaze ophiolite, southern Tibet: Constraints on its formation setting (United States)

    Zhang, Liang-Liang; Liu, Chuan-Zhou; Wu, Fu-Yuan; Zhang, Chang; Ji, Wei-Qiang; Wang, Jian-Gang


    The Cretaceous Xigaze ophiolite is best exposed at the central part of the Yarlung-Zangbo Suture Zone, Tibet Plateau. It consists of a thick section of mantle peridotites, but a relatively thin mafic sequence. This study presents geochronological and geochemical data for intrusive dykes (both mafic and felsic) and basalts to revisit the formation setting of the Xigaze ophiolite. The rodingites are characterized by high CaO and low Na2O contents relative to mafic dykes and show big variations in trace element compositions. Both gabbros and diabases have similar geochemical compositions, with MgO contents of 6.42-11.48 wt% and Mg# of 0.56-0.71. They display REE patterns similar to N-MORB and are variably enriched in large ion lithophile elements. Basalts have fractionated compositions and display LREE-depleted patterns very similar to N-MORB. They do not show obvious enrichment in LILE and depletion in high-field-strength elements, but a negative Nb anomaly is present. The studied plagiogranites have compositions of trondhjemite to tonalite, with high Na2O and low K2O contents. They have low TiO2 contents less than 1 wt%, consistent with melts formed by anatexis of gabbros rather than by differentiation of basalts. Zircons from seven samples, including three rodingites, three plagiogranites, and one gabbro, have been dated and yielded U-Pb ages of 124.6 ~ 130.5 Ma, indicating the Xigaze ophiolite was formed during the Early Cretaceous. They have mantle-like δ18O values of + 4.92 ~ + 5.26‰ and very positive εHf(t) values of + 16 ~ + 13.3. Ages of the rodingites and less altered gabbros indicate that serpentinization was occurred at ~ 125 Ma. Occurrence of both gabbroic and diabase dykes within the serpentinites suggests that the mantle lithosphere of the Xigaze ophiolite was rapidly exhumed. Both mafic and felsic dykes have slightly more radiogenic 87Sr/86Sr ratios relative to MORB, but depleted Hf-Nd isotpe compositions. They have a limited range of ε

  11. Near Surface CO2 Triple Oxygen Isotope Composition

    Directory of Open Access Journals (Sweden)

    Sasadhar Mahata


    Full Text Available The isotopic composition of carbon dioxide in the atmosphere is a powerful tool for constraining its sources and sinks. In particular, the 17O oxygen anomaly [Δ17O = 1000 × ln(1 + δ17O/1000 - 0.516 × 1000 × ln(1 + δ18O/1000], with a value > 0.5‰ produced in the middle atmosphere, provides an ideal tool for probing the exchange of carbon dioxide between the biosphere/hydrosphere and atmosphere. The biosphere/hydrosphere and anthropogenic emissions give values ≤ 0.3‰. Therefore, any anomaly in near surface CO2 would reflect the balance between stratospheric input and exchange with the aforementioned surface sources. We have analyzed Δ17O values of CO2 separated from air samples collected in Taipei, Taiwan, located in the western Pacific region. The obtained mean anomaly is 0.42 ± 0.14‰ (1-σ standard deviation, in good agreement with model prediction and a published decadal record. Apart from typically used δ13C and δ18O values, the Δ17O value could provide an additional tracer for constraining the carbon cycle.

  12. Monitoring the water vapor isotopic composition in the temperate North Atlantic (United States)

    Sveinbjörnsdottir, Arny E.; Steen-Larsen, Hans Christian; Jonsson, Thorsteinn; Johnsen, Sigfus J.


    Water stable isotopes have during many decades been used as climate proxies and indicators for variations in the hydrological cycle. However we are to a great extent still using simple empirical relationships without any deeper theoretical understanding. In order to properly relate changes in the climate and hydrological cycle to changes in the observed stable water isotopic signal we must understand the underlying physical processes. Furthermore it is a challenge for General Climate Models to adequately represent the isotopes in the hydrological cycle because of lack of in-situ measurements of the atmospheric water-vapor composition in the source regions. During the fall of 2010 we installed an autonomous water vapor spectroscopy laser (from Los Gatos Research) in a lighthouse on the South Coast of Iceland (63.83 N 21.47W) with the plan to be operational for several years. The purpose of this installation was through monitoring of the water vapor isotopic composition to understand the physical processes governing the isotopic composition of the water vapor evaporated from the ocean as well as the processes of mixing between the free troposphere and marine boundary layer. Because of the remoteness of the monitoring site and simple topography we are able to isolate the 'fingerprint' on the isotopic signal in the water vapor from respectively the ocean and the interior highland leading to a near perfect case-study area. Using back-trajectories we find a strong influence of the origin of the air masses on the measured isotopic composition. The mixing of the marine-boundary layer is found to strongly influence the measured isotopic composition. The second order isotopic parameter, d-excess, is contrary to theory and previous observations found not to depend on the relative humidity. However we do find a good correlation between the d-excess and the measured isotopic composition. We speculate that the lack of correlation between d-excess and relative humidity can be

  13. Isotopic composition of Pb and Th in interplinian volcanics from Somma-Vesuvius volcano, Italy (United States)

    Cortini, M.; Ayuso, R.A.; de Vivo, B.; Holden, P.; Somma, R.


    We present a detailed isotopic study of volcanic rocks emitted from Somma-Vesuvius volcano during three periods of interplinian activity: "Protohistoric" (3550 y B.P. to 79 A.D.), "Ancient Historic" (79 to 472 A.D.) and "Medieval" (472 to 1631 A.D.). Pb isotopic compositions of two acid leached fractions and whole rock residues of 37 whole rock samples (determined by Somma et al., 2001) show that each of the three interplinian periods is distinguished by small, systematic, and unique uranogenic and thorogenic Pb isotopic trends. This key and novel feature is compatible with the notion that the Pb isotopic data reflect small-scale source heterogeneity operating over relatively short periods of time. From this representative group of samples, a selected set of nine whole rocks were analysed for Th isotopes. 232Th/238U ratios in the source can be obtained independently from Pb and from Th isotopes. Those obtained from Pb isotopes represent source ratios, time-integrated over the whole age of the Earth; they range from 3.9 to 4.1. 232Th/238U obtained from Th isotopes are those of the present source. They are lower, and cluster around 3.5; this difference probably indicates recent U enrichment of the present source. The behaviour of Pb, as inferred by its isotopic ratios, is quite distinct from that of Sr and Nd isotopes: Pb isotope variations are not correlated to Sr or Nd isotope variations. The isotopic contrast is compatible with the idea that the isotopes were decoupled during magmatic production, evolution, and ascent through the crust. Thus, the Pb isotopes do not reflect the effects of the same processes as in the case of the Sr and Nd isotopes, or, as we also favor, they do not necessarily reflect the same source contributions into the magmas. Moreover, the Pb isotopic evolution of the interplinian rocks chiefly reflects mixing, driven by processes that are superimposed on, and independent of, other source contributions that determine the isotopic compositions

  14. Natural isotopic composition of nitrogen in suspended particulate matter in the Bay of Bengal

    Digital Repository Service at National Institute of Oceanography (India)

    Kumar, S.; Ramesh, R.; Bhosle, N.B.; Sardessai, S.; Sheshshayee, M.S.

    The first measurements of nitrogen isotopic composition (delta sup(15) N) in suspended particulate matter (SPM) of the surface Bay of Bengal (BOB) at 24 different locations during pre- (April-May 2003) and post- (September-October 2002) monsoon...

  15. Evolution of Organic Molecules in Space: Characterization and Isotope Composition of Experimental Analogues (United States)

    Piani, L.; Tachibana, S.; Hama, T.; Endo, Y.; Fujita, K.; Nakatsubo, S.; Fukushi, H.; Mori, S.; Chigai, T.; Yurimoto, H.; Kouchi, A.


    Laboratory experiments are conducted to investigate the organic compound formation in molecular cloud conditions and its evolution through UV irradiation and heating. A particular attention is given to the isotope composition of the organic residue.

  16. Usage of burnt fuel isotopic compositions from engineering codes in Monte-Carlo code calculations

    Energy Technology Data Exchange (ETDEWEB)

    Aleshin, Sergey S.; Gorodkov, Sergey S.; Shcherenko, Anna I. [Nuclear Research Centre ' ' Kurchatov Institute' ' , Moscow (Russian Federation)


    A burn-up calculation of VVER's cores by Monte-Carlo code is complex process and requires large computational costs. This fact makes Monte-Carlo codes usage complicated for project and operating calculations. Previously prepared isotopic compositions are proposed to use for the Monte-Carlo code (MCU) calculations of different states of VVER's core with burnt fuel. Isotopic compositions are proposed to calculate by an approximation method. The approximation method is based on usage of a spectral functionality and reference isotopic compositions, that are calculated by engineering codes (TVS-M, PERMAK-A). The multiplication factors and power distributions of FA and VVER with infinite height are calculated in this work by the Monte-Carlo code MCU using earlier prepared isotopic compositions. The MCU calculation data were compared with the data which were obtained by engineering codes.

  17. 鄂东南地区存在古元古代-太古宙基底--来自铜鼓山岩体锆石U-Pb-Hf同位素的证据%Paleoproterozoic-Archean Basement Beneath Southeast Hubei Province:Evidence from U-Pb-Hf Isotopes in Zircons from the Tonggushan Pluton

    Institute of Scientific and Technical Information of China (English)

    夏金龙; 黄圭成; 丁丽雪; 吴昌雄; 祝敬明; 金尚刚


    This paper has reported the integrated study of zircon U-Pb age and Lu-Hf isotope composition in zircons from the Tonggushan pluton, southeast Hubei Province. Tonggushan pluton is composed of quartz diorite porphyry. The 206Pb/238U mean age of magmatic zircon is (147±2.6) Ma, indicating that Tonggushan pluton was formed in the Late Jurassic-Early Cretaceous, which is consistent with the formation time of other plutons in this area. A large number of inherited zircons, formed in 1798~2888 Ma, exist in Tonggushan pluton. The Paleoproterozoic zircons are of magmatic origin and have similar 176Hf/177Hf and 176Lu/177Hf ratios, suggesting that they were probably derived from the same igneous basement rock. The Paleoproterozoic zircons have low Hf-isotope compositions and characteristics of crustal source. Hf model ages of these zircons and the presence of older inherited cores within them suggest that the source of Paleoproterozoic magma was Neoarchaean crust, implying the existence of an unexposed old basement beneath southeast Hubei Province and the whole Yangtze block. These data supply new clue to the study of the Precambrian basement evolution of Yangtze block. The Paleoproterozoic-Archean basement of the Yangtze Block most likely spreads from the Sichuan Basin through western Huebei Province to southeastern Hubei Province.%对鄂东南地区位于毛铺-两剑桥断裂带上的铜鼓山岩体进行了野外地质及镜下显微研究及岩石化学分析,重点分析了其中锆石U-Pb年龄和Hf同位素组成。结果表明铜鼓山岩体为石英闪长玢岩,岩体形成于(147±2.6) Ma,属晚侏罗世-早白垩世,与鄂东南地区其它岩体年龄具有一致性。铜鼓山岩体中存在的大量继承锆石。分析的4个继承锆石形成于古元古代晚期1798~1888 Ma。继承锆石具有高的Th/U比值和极其相似的Lu-Hf同位素组成,表明它们捕获于同一火成岩。这表明鄂东南地区存在古元古代基底。这些古元古代

  18. Carbon and hydrogen isotopic composition and generation pathway of biogenic gas in China

    Institute of Scientific and Technical Information of China (English)

    SHEN Ping; WANG Xiaofeng; XU Yin; SHI Baoguang; XU Yongchang


    The carbon and hydrogen isotopic composition of biogenic gas is of great importance for the study of its generation pathway and reservoiring characteristics. In this paper, the formation pathways and reservoiring characteristics of biogenic gas reservoirs in China are described in terms of the carbon and hydrogen isotopic compositions of 31 gas samples from 10 biogenic gas reservoirs. The study shows that the hydrogen isotopic compositions of these biogenic gas reservoirs can be divided into three intervals:δDCH4>-200‰,-250‰<δDCH4<-200‰ and δDCH4<-250‰. The forerunners believed that the main generation pathway of biogenic gas under the condition of continental fresh water is acetic fermentation. Our research results showed that the generation pathway of biogenic gas under the condition of marine facies is typical CO2- reduction, the biogenic gas has heavy hydrogen isotopic composition: its δDCH4 values are higher than -200‰; that the biogenic gas under the condition of continental facies also was generated by the same way, but its hydrogen isotopic composition is lighter than that of biogenetic gas generated under typical marine facies condition: -250‰<δDCH4<-200‰, the δDCH4 values may be related to the salinity of the water medium in ancient lakes. From the relevant data of the Qaidam Basin, it can be seen that the hydrogen isotopic composition of biogenic methane has the same variation trend with increasing salinity of water medium. There are biogenic gas reservoirs formed in transitional regions under the condition of continental facies. These gas reservoirs resulted from both CO2- reduction and acetic fermentation, the formation of which may be related to the non-variant salinity of ancient water medium and the relatively high geothermal gradient, as is the case encountered in the Baoshan Basin. The biogenic gas generating in these regions has light hydrogen isotopic composition: δDCH4<-250‰, and relatively heavy carbon isotopic

  19. The tungsten isotopic composition of Eoarchean rocks: Implications for early silicate differentiation and core-mantle interaction on Earth (United States)

    Iizuka, Tsuyoshi; Nakai, Shun'ichi; Sahoo, Yu Vin; Takamasa, Asako; Hirata, Takafumi; Maruyama, Shigenori


    We have measured 182W/ 184W for Eoarchean rocks from the Itsaq Gneiss Complex (3.8-3.7 Ga pillow meta-basalts, a meta-tonalite, and meta-sediments) and Acasta Gneiss Complex (4.0-3.6 Ga felsic orthogneisses) to assess possible W isotopic heterogeneity within the silicate Earth and to constrain W isotopic evolution of the mantle. The data reveal that 182W/ 184W values in the Eoarchean samples are uniform within the analytical error and indistinguishable from the modern accessible mantle signature, suggesting that the W isotopic composition of the upper mantle has not changed significantly since the Eoarchean era. The results imply either that chemical communication between the mantle and core has been insignificant in post-Hadean times, or that a lowermost mantle with a distinctive W isotope signature has been isolated from mantle convective cycling. Most terrestrial rock samples have a 0.2 ɛ142Nd/ 144Nd higher than the chondrite average. This requires either the presence of a hidden enriched reservoir formed within the first 30 Ma of the Solar System, or the bulk Earth having a ˜ 5% higher Sm/Nd than the chondrite average. We explored the relevance of the 182Hf- 182W isotope system to the 146Sm- 142Nd isotope system during early silicate differentiation events on Earth. In this context, we demonstrate that the lack of resolvable 182W excesses in the Itsaq rocks, despite 142Nd excesses compared to the modern accessible mantle, is more consistent with the view that the bulk Earth has a non-chondritic Sm/Nd. In the non-chondritic Sm/Nd Earth model, the 182W- 142Nd chronometry constrains the age of the source mantle depletion for the Itsaq samples to more than ˜ 40 Ma after the Solar System origin. Our results cannot confirm the previous report of 182W anomalies in the Eoarchean Itsaq meta-sediments, which were interpreted as reflecting an impact-derived meteoritic component.

  20. Non-destructive measurement of carbonic anhydrase activity and the oxygen isotope composition of soil water (United States)

    Jones, Sam; Sauze, Joana; Ogée, Jérôme; Wohl, Steven; Bosc, Alexandre; Wingate, Lisa


    Carbonic anhydrases are a group of metalloenzymes that catalyse the hydration of aqueous carbon dioxide (CO2). The expression of carbonic anhydrase by bacteria, archaea and eukarya has been linked to a variety of important biological processes including pH regulation, substrate supply and biomineralisation. As oxygen isotopes are exchanged between CO2 and water during hydration, the presence of carbonic anhydrase in plants and soil organisms also influences the oxygen isotope budget of atmospheric CO2. Leaf and soil water pools have distinct oxygen isotope compositions, owing to differences in pool sizes and evaporation rates, which are imparted on CO2during hydration. These differences in the isotopic signature of CO2 interacting with leaves and soil can be used to partition the contribution of photosynthesis and soil respiration to net terrestrial CO2 exchange. However, this relies on our knowledge of soil carbonic anhydrase activity and currently, the prevalence and function of these enzymes in soils is poorly understood. Isotopic approaches used to estimate soil carbonic anhydrase activity typically involve the inversion of models describing the oxygen isotope composition of CO2 fluxes to solve for the apparent, potentially catalysed, rate of oxygen exchange during hydration. This requires information about the composition of CO2 in isotopic equilibrium with soil water obtained from destructive, depth-resolved soil water sampling. This can represent a significant challenge in data collection given the considerable potential for spatial and temporal variability in the isotopic composition of soil water and limited a priori information with respect to the appropriate sampling resolution and depth. We investigated whether we could circumvent this requirement by constraining carbonic anhydrase activity and the composition of soil water in isotopic equilibrium with CO2 by solving simultaneously the mass balance for two soil CO2 steady states differing only in the

  1. Spatiotemporal variation of stable isotopic composition in precipitation

    DEFF Research Database (Denmark)

    Müller, Sascha; Stumpp, Christine; Sørensen, Jens Havskov


    gradient and predominant westerly winds. Data showed the local meteoric water line for this region is expressed by the equation δ2H = 7.4δ18O + 5.4‰. A significant trend correlating enriched isotopic values to humidities around 70% during dry season and more depleted isotopic values to humidities around 90...

  2. Spatial gradients in the isotopic composition of paleoprecipitation for terrestrial climate and altimetry studies (United States)

    Chamberlain, C. P.; Winnick, M.; Ibarra, D. E.; Caves, J. K.; Ritch, A. J.


    The oxygen and hydrogen isotopic composition of authigenic minerals in terrestrial sediments provides one of the critical measures of past climate change. Frequently, these measurements are made at single sites to determine how climate and/or topography have changed over specific time intervals of interest. We argue here that spatial gradients in the oxygen and hydrogen isotope of precipitation along specific storm tracks provide a more powerful method to determine changes in paleoclimate and paleotopography. We use a nondimensional isotopic vapor transport model coupled with a soil water isotope model to evaluate how moisture recycling and the relative role of eddy diffusion and advective transport of water vapor affect horizontal isotopic gradients on continents. Relatively large changes in the isotopic composition of precipitation can occur by changes in water balance and the transport mechanism of water vapor - certainly as high as can be induced by the uplift of major mountain belts and large changes in global/regional temperature. As an example, we point to Miocene to Recent oxygen isotopic records of paleo-mid latitude sediments that tend to increase with time, globally. We suggest that this increase in the oxygen isotope of precipitation is the result of increased aridity and the expansion of grasslands during the Miocene. Further, we suggest that many of the Miocene to Recent isotopic records collected in the mountainous regions of Central Asia, Western North America, and South America reflect changes in water balance that are, in part, independent of changes in surface topography.

  3. Long-term data set analysis of stable isotopic composition in German rivers (United States)

    Reckerth, Anne; Stichler, Willibald; Schmidt, Axel; Stumpp, Christine


    Stable isotopes oxygen-18 (18O) and deuterium (2H) are commonly used to investigate hydrological processes in catchments. However, only a few isotope studies have been conducted on a large scale and rarely over long time periods. The objective of this study was to identify the spatial and seasonal variability of isotopic composition in river water and how it is affected by geographical and hydrological factors. The stable isotopic composition of river water has been measured in nine large river catchments in Germany for a time period of 12 years or 26 years. We conducted time series and correlation analyses to identify spatial and temporal patterns of the isotopic composition in the rivers. Further, we compared it to isotopic composition in local precipitation and catchments characteristics. In the majority of the rivers, the spatial and temporal patterns of precipitation were directly reflected in river water. The isotopic signals of the river water were time shifted and show attenuated amplitudes. Further deviations from isotopic compositions in local precipitation were observed in catchments with complex flow systems. These deviations were attributed to catchment processes and influences like evaporation, damming and storage. The seasonality of the isotopic composition was mainly determined by the discharge regimes of the rivers. We found correlations between isotopic long-term averages and catchment altitude as well as latitude and longitude, resulting in a northwest-southeast gradient. Furthermore, it was shown that long-term averages of d-excess were inversely related to flow length and catchment size, which indicates that evaporation enrichment has an impact on the isotopic composition even in catchments of humid climates. This study showed that isotopic composition in rivers can serve as a proxy for the local precipitation and can be utilized as an indicator for hydrological processes even in large river basins. In future, such long time series will help to

  4. Elemental and iron isotopic composition of aerosols collected in a parking structure. (United States)

    Majestic, Brian J; Anbar, Ariel D; Herckes, Pierre


    The trace metal contents and iron isotope composition of size-resolved aerosols were determined in a parking structure in Tempe, AZ, USA. Particulate matter (PM)2.5 microm were collected. Several air toxics (e.g., arsenic, cadmium, and antimony) were enriched above the crustal average, implicating automobiles as an important source. Extremely high levels of fine copper (up to 1000 ng m(-3)) were also observed in the parking garage, likely from brake wear. The iron isotope composition of the aerosols were found to be +0.15+/-0.03 per thousand and +0.18+/-0.03 per thousand for the PM2.5 microm fractions, respectively. The similarity of isotope composition indicates a common source for each size fraction. To better understand the source of iron in the parking garage, the elemental composition in four brake pads (two semi-metallic and two ceramic), two tire tread samples, and two waste oil samples were determined. Striking differences in the metallic and ceramic brake pads were observed. The ceramic brake pads contained 10-20% copper by mass, while the metallic brake pads contained about 70% iron, with very little copper. Both waste oil samples contained significant amounts of calcium, phosphorous, and zinc, consistent with the composition of some engine oil additives. Differences in iron isotope composition were observed between the source materials; most notably between the tire tread (average=+0.02 per thousand) and the ceramic brake linings (average=+0.65 per thousand). Differences in isotopic composition were also observed between the metallic (average=+0.18 per thousand) and ceramic brake pads, implying that iron isotope composition may be used to resolve these sources. The iron isotope composition of the metallic brake pads was found to be identical to the aerosols, implying that brake dust is the dominant source of iron in a parking garage.

  5. Geochemistry, zircon U-Pb and Lu-Hf isotopes of an Early Cretaceous intrusive suite in northeastern Jiangxi Province, South China Block: Implications for petrogenesis, crust/mantle interactions and geodynamic processes (United States)

    Deng, Zhengbin; Liu, Shuwen; Zhang, Lifei; Wang, Zongqi; Wang, Wei; Yang, Pengtao; Luo, Ping; Guo, Boran


    The Early Cretaceous Tieshan intrusive suite, in northeastern Jiangxi Province along the northern margin of the Eastern Cathaysia Block, is composed of diabase porphyrites, monzodiorites, syenite porphyries, quartz monzonites, monzogranites and granite porphyries. LA-ICPMS zircon U-Pb isotopic analyses reveal that this intrusive complex was emplaced between 142 Ma and 117 Ma. The ~ 135 Ma diabase porphyrites, monzodiorites, and syenite porphyries are characterized by low to moderate SiO2 and MgO contents, with high K2O and total alkaline contents. These rocks exhibit slightly to strongly fractionated REE patterns and upper crust-like multi-element patterns with depletions of Nb, Ta and Ti, and show strongly negative εHf (t) values of - 9.0 to - 11.8. All these patterns are identical to those of the Caiyuan syenites, Huangtuling gabbros in the east, and Lengshuikeng trachyandesites and quartz syenites in the west. These geochemical and zircon Lu-Hf isotopic features indicate that their magmatic precursors were generated by 0.2%-2% partial melting of a phlogopite-bearing enriched subcontinental lithospheric mantle source that was metasomatized by sediments. The ~ 117 Ma quartz monzonite has slightly higher εHf (t) values (- 5.6 to - 8.7) like those of the Honggong syenites, indicating an interaction between the asthenosphere and the lithosphere. The ~ 142-134 Ma granite porphyries and monzogranites are characterized by high SiO2 levels but low concentrations of refractory elements, and show enrichment of LREEs and LILEs, with variable negative anomalies of Nb, Ta, Ti, Sr, P and Ba in multi-element diagrams normalized by primitive mantle. The monzogranite exhibits strongly negative εHf (t) values of - 10.5 to - 13.3 and TDM2 (Hf) values of 1849-2023 Ma, and the granite porphyries display relatively wide εHf (t) values of - 7.2 to - 13.4 and TDM2 (Hf) values of 1645-2043 Ma, indicating that these monzogranites and granite porphyries are highly fractionated granites

  6. The oxygen isotope composition of dissolved anthropogenic phosphates: a new tool for eutrophication research? (United States)

    Gruau, Gérard; Legeas, Michèle; Riou, Christine; Gallacier, Eve; Martineau, François; Hénin, O


    High-precision oxygen isotope analyses were carried out on dissolved phosphate extracted from discharge waters from three wastewater treatment plants (WTP) located in western France, as well as on the different phosphate-based fertilizers applied by farmers in the same region. Measured delta(18)O values of phosphate from chemical fertilizers range from 19.6 to 23.1 per thousand, while those of phosphate from WTP discharge waters are more tightly grouped between 17.7 and 18.1 per thousand. The variability in delta(18)O values of phosphate fertilizers is attributed to oxygen isotope variations of the phosphorite deposits from which France's fertilizers are manufactured. The significance of the delta(18)O values of phosphate from WTP discharge waters is less straightforward. At present, it is not clear whether these values are primary isotopic compositions corresponding, e.g., to the oxygen isotope composition of phosphate builders included in detergents (delta(18)O(P)=17.9 per thousand), or represent secondary values reflecting biological recycling of the phosphate in equilibrium with ambient WTP water The restricted difference in isotopic composition obtained between phosphate from fertilizers and phosphate from WTP discharge waters (isotopic variability observed in both end-members (>/=1.5 per thousand), cast doubt about the possibility that the oxygen isotope composition could serve as a tracer for the source of anthropogenic phosphates in waters.

  7. Carbon and oxygen isotope compositions of the carbonate facies in the Vindhyan Supergroup, central India

    Indian Academy of Sciences (India)

    S Banerjee; S K Bhattacharya; S Sarkar


    The Vindhyan sedimentary succession in central India spans a wide time bracket from the Paleopro- terozoic to the Neoproterozoic period.Chronostratigraphic significance of stable carbon and oxygen isotope ratios of the carbonate phase in Vindhyan sediments has been discussed in some recent studies.However,the subtle controls of facies variation,depositional setting and post-depositional diagenesis on stable isotope compositions are not yet clearly understood.The Vindhyan Super- group hosts four carbonate units,exhibiting a wide variability in depositional processes and paleogeography.A detailed facies-specific carbon and oxygen isotope study of the carbonate units was undertaken by us to investigate the effect of these processes and to identify the least altered isotope values.It is seen that both carbon and oxygen isotope compositions have been affected by early meteoric water diagenesis.The effect of diagenetic alteration is,however,more pronounced in case of oxygen isotopes than carbon isotopes.Stable isotope compositions remained insensitive to facies only when sediments accumulated in a shallow shelf setting without being exposed.Major alteration of original isotope ratios was observed in case of shallow marine carbonates,which became exposed to meteoric fluids during early diagenetic stage.Duration of exposure possibly determined the magnitude of alteration and shift from the original values.Moreover,dolomitization is found to be accompanied by appreciable alteration of isotope compositions in some of the carbonates.The present study suggests that variations in sediment depositional settings,in particular the possibility of subaerial exposure,need to be considered while extracting chronostratigraphic signi ficance from 13C data.

  8. Variations in isotopic compositions of chlorine in evaporation-controlled salt lake brines of Qaidam Basin, China

    Digital Repository Service at National Institute of Oceanography (India)

    Xiao, Ying-kai; Liu, Wei-guo; Zhou, Y.M.; Wang, Yun-hui; Shirodkar, P.V.

    The variations in the isotopic compositions of chlorine in evaporation-controlled saline lake brines were determined by using an improved procedure for precise measurement of chlorine isotopes based on Cs sub(2) Cl sup(+) ion by thermal ionization...

  9. Oxygen isotopic composition of low-temperature authigenic clinoptilolite (United States)

    Nähr, T.; Botz, R.; Bohrmann, G.; Schmidt, M.


    Oxygen isotope ratios were obtained from authigenic clinoptilolites from Barbados Accretionary Complex, Yamato Basin, and Exmouth Plateau sediments (ODP Sites 672, 797, and 762) in order to investigate the isotopic fractionation between clinoptilolite and pore water at early diagenetic stages and low temperatures. Dehydrated clinoptilolites display isotopic ratios for the zeolite framework ( δ18O f) that extend from +18.7‰ to +32.8‰ (vs. SMOW). In combination with associated pore water isotope data, the oxygen isotopic fractionation between clinoptilolite and pore fluids could be assessed in the temperature range from 25°C to 40°C. The resulting fractionation factors of 1.032 at 25°C and 1.027 at 40°C are in good agreement with the theoretically determined oxygen isotope fractionation between clinoptilolite and water. Calculations of isotopic temperatures illustrate that clinoptilolite formation occurred at relatively low temperatures of 17°C to 29°C in Barbados Ridge sediments and at 33°C to 62°C in the Yamato Basin. These data support a low-temperature origin of clinoptilolite and contradict the assumption that elevated temperatures are the main controlling factor for authigenic clinoptilolite formation. Increasing clinoptilolite δ18O f values with depth indicate that clinoptilolites which are now in the deeper parts of the zeolite-bearing intervals had either formed at lower temperatures (17-20°C) or under closed system conditions.

  10. Magnesium isotopic composition of the oceanic mantle and oceanic Mg cycling (United States)

    Liu, Ping-Ping; Teng, Fang-Zhen; Dick, Henry J. B.; Zhou, Mei-Fu; Chung, Sun-Lin


    To constrain the Mg isotopic composition of the oceanic mantle, investigate Mg isotope fractionation of abyssal peridotites during seafloor alteration, and assess Mg budget in the oceans, a suite of 32 abyssal peridotite samples from the Gakkel Ridge and Southwest Indian Ridge (SWIR) was, for the first time, selected for high-precision Mg isotope analyses. Although most of these samples are extensively altered, largely by serpentinization and weathering, primary olivine, diopside and enstatite grains are preserved in some samples. Olivine grains from the least altered samples have δ26Mg varying from -0.30 to -0.12‰ (n = 7), whereas enstatite and diopside have δ26Mg varying from -0.27 to -0.16‰ (n = 7), and from -0.23 to -0.09‰ (n = 6), respectively. Whole-rock δ26Mg values range from -0.24 to 0.03‰ with an average of -0.12 ± 0.13‰ (2SD, n = 32). Strongly serpentinized peridotites have lower average δ26Mg values (δ26Mg = -0.19 ± 0.07‰, 2SD, n = 7) than weathering-dominated ones (δ26Mg = -0.10 ± 0.12‰, 2SD, n = 25). Calculated Mg isotopic compositions of fresh mantle peridotites vary from -0.29 to -0.13‰, beyond the previously reported range of the subcontinental lithospheric mantle (-0.25 ± 0.04‰) and the analytical uncertainty (±0.07‰, 2SD). Our study therefore indicates that the oceanic mantle may have similar but slightly heterogeneous Mg isotopic compositions to that of subcontinental lithospheric mantle. Secondary serpentinization does not fractionate Mg isotopes of abyssal peridotites, whereas low-T weathering and formation of clay can result in the enrichment of heavy Mg isotopes in abyssal peridotites. This study also demonstrates that fluid-rock interaction does not necessarily produce rocks with intermediate Mg isotopic compositions. Magnesium isotopes of the rocks thereafter are dependent on the secondary minerals formed. We also conclude that the release of light Mg isotopes into the ocean during alteration of abyssal

  11. Abyssal peridotites reveal the near-chondritic Fe isotopic composition of the Earth (United States)

    Craddock, Paul R.; Warren, Jessica M.; Dauphas, Nicolas


    Terrestrial oceanic and continental basalts are enriched by approximately +0.1‰ in 56Fe/54Fe ratio relative to primitive, undifferentiated meteorites (chondrites). The δ56Fe values of terrestrial basalts are also distinct from those of basalts from Mars and asteroid Vesta, which have chondritic Fe isotopic compositions. The processes responsible for the isotopic enrichment of terrestrial basalts are debated, in part because the Fe isotopic composition of the mantle source of terrestrial basalts is unknown. Here we report Fe isotopic measurements of abyssal peridotites, which are the residues of limited melting at oceanic ridges and are thus the best proxies for the composition of the convective portion of the mantle. Our data show that abyssal peridotites have a mean δ56Fe value of +0.010±0.007‰ (relative to IRMM-014), which is indistinguishable from chondrites. After correcting this data for seafloor weathering and mantle melting, we estimate the average Fe isotopic composition of the terrestrial mantle to be δ56Fe=+0.025±0.025‰, which is also indistinguishable from chondrites, within current analytical precision. We determine that the maximum shift in δ56Fe for peridotite residues during partial mantle melting is 0.01‰. Our results argue against isotopic fractionation during core-mantle differentiation or iron vaporization during the Moon-forming giant impact, because both processes would yield a bulk mantle δ56Fe value that is non-chondritic. In addition, our results suggest that disproportionation of mantle Fe2+-Fe3+ in perovskite and Fe0 metal and segregation of metal to the core could not have been a driver for Fe isotopic fractionation in the silicate mantle. Instead, the different iron isotopic compositions of abyssal peridotites and MORBs support mounting evidence for iron isotopic fractionation of melts but not residues during the formation of oceanic and continental crust.

  12. Isotopic composition of Lake Agassiz-Ojibway water just prior to final drainage (United States)

    Hillaire-Marcel, C.; Helie, J.; McKay, J.; Lalonde, A.


    Controversies persist with respect to the impact of the final drainage of Lake Agassiz-Ojibway on the thermohaline circulation of the North Atlantic, some 8.4 ka ago. The lack of response of planktic foraminifer isotope records, off Hudson Strait (i.e., at the outlet of the drainage channel) constitutes one of the most puzzling elements in this debate. However, data on the isotopic composition of drainage waters are needed to estimate the response of the 18-O-salinity relationship in NW Atlantic surface waters. In the literature, a large array of isotopic compositions have been suggested, notably for modeling experiment purposes. Scattered information about the isotopic composition of Lake Agassiz water does exist. It includes isotopic measurements of pore waters of lacustrine sediments [1], analyses of oxygen isotopes in cellulose from algal or plant remains [2], and stable isotope compositions of concretions from varves [3]. Whereas, relatively low oxygen isotope values (apx. -25 per mil vs. VSMOW) are inferred for Lake Agassiz waters during cold pulses of the deglaciation, most data suggest much higher values during the final stages of Lake Agassiz-Ojiway, just prior to its drainage. Calcareous concretions from Lake Ojibway varves (not necessarily contemporaneous to the lacustrine stage) yielded oxygen isotope compositions of about -10 per mil (vs. VPDB), suggesting values as high as -14 per mil (vs. VSMOW) for pore waters (assuming a 0-4 degrees C temperature range). Similar high values (as high as -8 per mil vs. VSMOW [1]) were also estimated from pore water analyses of contemporaneous Lake Agassiz sediments. Here, we used a core raised from Eastern Hudson Bay, off Great Whale River, to further document isotopic compositions of the lake waters prior to their drainage into the North Atlantic. The 7.40 m long core has an apx. 1.3 m-thick lacustrine layer at its base, including the drainage sub- layer. It is overlain by Tyrrell Sea clays. Scarce valves of Candona

  13. Barren Miocene granitoids in the Central Andean metallogenic belt, Chile: Geochemistry and Nd-Hf and U-Pb isotope systematics Granitoides estériles del Mioceno en la franja metalogénica de los Andes Centrales, Chile: geoquímica e isotopía de Nd-Hf y U-Pb

    Directory of Open Access Journals (Sweden)

    Katja Deckart


    Full Text Available Four Middle-to-Late Miocene barren plutonic complexes that occur between the giant porphyry copper deposits of the central Chilean Andes were selected for U-Pb LA-ICPMS geochronology and Hf-isotope systematics on single zircon grains. Major and trace elements and Sr-Nd-Hf isotope whole rock geochemical studies were under-taken to compare with slightly younger or coeval barren and fertile intrusive rocks between 32° and 34°S. The studied granitoids yield resolvable crystallization ages of 11.3±0.1 Ma (Cerro Mesón Alto massif, 10.3±0.2 Ma (La Gloria pluton, 14.9±0.2 Ma/14.9±0.1 Ma (Yerba Loca stock and 11.2±0.1 Ma/14.7±0.1 Ma (San Francisco Batholith. Major and trace elements discard an adakitic signature as suggested for coeval porphyric intrusions at 32°S, slightly younger mineralized porphyries at Río Blanco-Los Bronces deposit and other Cenozoic adakites. Volcanic host rocks are less fractionated than the intrusive rock units. The same observation can be made for the unmineralized northern plutons compared to the southern ones. Initial Sr-Nd isotope data show insignificant variation (0.703761-0.704118 and 0.512758-0.512882, plotting in the mantle array. Trace element enrichment can be explained by addition of subducted-slab fluids and/or terrigenous sediments to the mantle wedge prior to and/or slight crustal input during magma ascent. Zircon grains separated from these barren intrusives share a similar initial εHf i-data variation for the younger age group (10-12 Ma; 7.04-9.54 and show a more scattered range for the older one (14-15 Ma; 8.50-15.34; both sets plot between the DM and CLTUR evolution lines. There is evidence that magma evolution was slightly distinct through time from older to younger barren magmatism, compared to a few fertile porphyritic rocks from Río Blanco-Los Bronces porphyry copper deposit. It is suggested that chronological inconsistencies within these complexes might be related to differential shortening

  14. Stable isotopic composition of perchlorate and nitrate accumulated in plants: Hydroponic experiments and field data (United States)

    Estrada, Nubia Luz; Böhlke, John Karl; Sturchio, Neil C.; Gu, Baohua; Harvey, Greg; Burkey, Kent O.; Grantz, David A.; McGrath, Margaret T.; Anderson, Todd A.; Rao, Balaji; Sevanthi, Ritesh; Hatzinger, Paul B.; Jackson, W. Andrew


    Natural perchlorate (ClO4−) in soil and groundwater exhibits a wide range in stable isotopic compositions (δ37Cl, δ18O, and Δ17O), indicating that ClO4− may be formed through more than one pathway and/or undergoes post-depositional isotopic alteration. Plants are known to accumulate ClO4−, but little is known about their ability to alter its isotopic composition. We examined the potential for plants to alter the isotopic composition of ClO4− in hydroponic and field experiments conducted with snap beans (Phaseolus vulgaris L.). In hydroponic studies, anion ratios indicated that ClO4− was transported from solutions into plants similarly to NO3− but preferentially to Cl− (4-fold). The ClO4− isotopic compositions of initial ClO4− reagents, final growth solutions, and aqueous extracts from plant tissues were essentially indistinguishable, indicating no significant isotope effects during ClO4− uptake or accumulation. The ClO4− isotopic composition of field-grown snap beans was also consistent with that of ClO4− in varying proportions from irrigation water and precipitation. NO3− uptake had little or no effect on NO3− isotopic compositions in hydroponic solutions. However, a large fractionation effect with an apparent ε (15N/18O) ratio of 1.05 was observed between NO3− in hydroponic solutions and leaf extracts, consistent with partial NO3− reduction during assimilation within plant tissue. We also explored the feasibility of evaluating sources of ClO4− in commercial produce, as illustrated by spinach, for which the ClO4− isotopic composition was similar to that of indigenous natural ClO4−. Our results indicate that some types of plants can accumulate and (presumably) release ClO4− to soil and groundwater without altering its isotopic characteristics. Concentrations and isotopic compositions of ClO4−and NO3− in plants may be useful for determining sources of fertilizers and sources of ClO4− in their growth environments and

  15. Dating the Indo-Asia collision in NW Himalaya: constraints from Sr-Nd isotopes and detrital zircon (U-Pb) and Hf isotopes of Paleogene-Neogene rocks in the Katawaz basin, NW Pakistan (United States)

    Zhuang, Guangsheng; Najman, Yani; Millar, Ian; Chauvel, Catherine; Guillot, Stephane; Carter, Andrew


    The time of collision between the Indian and Asian plates is key for understanding the convergence history and the impact on climatic systems and marine geochemistry. Despite much active research, the fundamental questions still remain elusive regarding when and where the Indian plate collided with the Asian plate. Especially in the west Himalaya, the questions become more complex due to disputes on the amalgamation history of interoceanic Kohistan-Ladakh arcs (KLA) with Karakoram of the Asian plate and the Indian plate. Here, we present a result of multiple-isotopic geochemistry and geochronology study in the Katawaz Basin in NW Pakistan, a remnant oceanic basin on the western Indian plate which was the repository for the sediments eroded from the west Himalaya ( Qayyum et al., 1996, 1997a, 1997b, 2001; Carter et al., 2010), to evaluate the time and character of collision in this region. In this study, we analyzed 22 bulk mudstone samples for Sr-Nd isotopes and 11 medium-grained sandstones for detrital zircon (U-Pb) geochronology and Hf isotopes. We constructed the Cenozoic chronology in the Katawaz Basin based on our newly collected detrital zircon U-Pb ages and fission track ages. We present the first record of Katawaz chronology that constrained the Khojak Formation to be current study revealed that the Katawaz sedimentary sequence ranges in age from Eocene to the earliest Miocene. The samples from the Nisai Formation show the 87Sr/86Sr - ɛNd values overlapping those of the end member of the Karakoram of Asian origin, revealing the arrival of Asian detritus on the Indian plate prior to 50 Ma. There are two parallel lines of evidence supporting this conclusion: (1) young zircon grains (Journal of the Geological Society 154, 753-756. Qayyum, M., Lawrence, R.D., Niem, A.R., 1997b. Molasse-Delta-flysch continuum of the Himalayan orogeny and closure of the Paleogene Katawaz Remnant Ocean, Pakistan. International geology review 39, 861-875. Qayyum, M., Niem, A

  16. Normal variations in the isotopic composition of metabolically relevant transition metals in human blood (United States)

    Van Heghe, L.; Cloquet, C.; Vanhaecke, F.


    Cu, Fe and Zn are transition metals with great catalytic, structural and regulating importance in the human body. Hence, an aberrant metabolism of these elements can have serious implications on the health of a person. It is assumed that, due to differences in isotope fractionation, the isotopic composition of these elements in whole blood of patients can be different from that in blood of healthy subjects. Therefore, isotopic analysis of the element affected by the disease can be a promising approach for early diagnosis. A method for isotopic analysis of Cu, Fe and Zn in human whole blood was developed. The simultaneous chromatographic isolation of these elements and the conditions for isotope ratio measurement via multi-collector ICP - mass spectrometry (MC-ICP-MS) were optimized. So far, only whole blood of supposedly healthy volunteers (reference population) was analyzed. Results for Fe confirmed the known differences in isotopic composition between male and female blood. It is also shown that other parameters can have influence as well, e.g., the isotopic composition of Zn seems to be governed by the diet.

  17. Zircon U-Pb age, Lu-Hf isotope, mineral chemistry and geochemistry of Sundamalai peralkaline pluton from the Salem Block, southern India: Implications for Cryogenian adakite-like magmatism in an aborted-rift (United States)

    Renjith, M. L.; Santosh, M.; Li, Tang; Satyanarayanan, M.; Korakoppa, M. M.; Tsunogae, T.; Subba Rao, D. V.; Kesav Krishna, A.; Nirmal Charan, S.


    The Sundamalai peralkaline pluton is one among the Cryogenian alkaline plutons occurring in the Dharmapuri Rift Zone (DRZ) of the Salem Block in the Southern Granulite Terrane (SGT) of India. Here we present zircon U-Pb age and Lu-Hf isotopic composition, mineral chemistry and geochemistry of the pluton to explore the petrogenesis and geodynamic implications. Systematic modal variation of orthoclase, Na-plagioclase, Ca-amphibole (ferro-edenite and hastingsite) and quartz developed quartz-monzonite and granite litho units in the Sundamalai pluton. Thermometry based on amphibole-plagioclase pair suggests that the pluton was emplaced and solidified at around 4.6 kbar pressure with crystallization of the major phases between 748 and 661 °C. Estimated saturation temperature of zircon (712-698 °C) is also well within this range. However, apatite saturation occurred at higher temperatures between 835 and 870 °C, in contrast with monazite saturation (718-613 °C) that continued up to the late stage of crystallization. Estimated oxygen fugacity values (log fO2: -14 to -17) indicate high oxidation state for the magma that stabilized titanite and magnetite. The magmatic zircons from Sundamalai pluton yielded a weighted mean 206Pb/238U age of 832.6 ± 3.2 Ma. Geochemically, the Sundamalai rocks are high-K to shoshonitic, persodic (Na2O/K2O ratio > 1), silica-saturated (SiO2:65-72 wt.%), and peralkaline in composition (aluminum saturation index, ASI effect) controlled differentiation between quartz-monzonite and granite. Both rock types have high content of Na2O (5.1-6.3 wt.%), Ba (350-2589 ppm) and Sr (264-1036 ppm); low content of Y (8.7-17 ppm) and Yb (0.96-1.69 ppm); elevated ratios of La/Yb (11-46) and Sr/Y (46-69) and are depleted in Ti, with a positive Sr anomaly suggesting an adakite-like composition and garnet controlled melting of a plagioclase-poor source. The low content of MgO (aborted rifting along the DRZ generating the magma that crystallized the Sundamalai

  18. The stable Cr isotopic compositions of chondrites and silicate planetary reservoirs (United States)

    Schoenberg, Ronny; Merdian, Alexandra; Holmden, Chris; Kleinhanns, Ilka C.; Haßler, Kathrin; Wille, Martin; Reitter, Elmar


    The depletion of chromium in Earth's mantle (∼2700 ppm) in comparison to chondrites (∼4400 ppm) indicates significant incorporation of chromium into the core during our planet's metal-silicate differentiation, assuming that there was no significant escape of the moderately volatile element chromium during the accretionary phase of Earth. Stable Cr isotope compositions - expressed as the ‰-difference in 53Cr/52Cr from the terrestrial reference material SRM979 (δ53/52CrSRM979 values) - of planetary silicate reservoirs might thus yield information about the conditions of planetary metal segregation processes when compared to chondrites. The stable Cr isotopic compositions of 7 carbonaceous chondrites, 11 ordinary chondrites, 5 HED achondrites and 2 martian meteorites determined by a double spike MC-ICP-MS method are within uncertainties indistinguishable from each other and from the previously determined δ53/52CrSRM979 value of -0.124 ± 0.101‰ for the igneous silicate Earth. Extensive quality tests support the accuracy of the stable Cr isotope determinations of various meteorites and terrestrial silicates reported here. The uniformity in stable Cr isotope compositions of samples from planetary silicate mantles and undifferentiated meteorites indicates that metal-silicate differentiation of Earth, Mars and the HED parent body did not cause measurable stable Cr isotope fractionation between these two reservoirs. Our results also imply that the accretionary disc, at least in the inner solar system, was homogeneous in its stable Cr isotopic composition and that potential volatility loss of chromium during accretion of the terrestrial planets was not accompanied by measurable stable isotopic fractionation. Small but reproducible variations in δ53/52CrSRM979 values of terrestrial magmatic rocks point to natural stable Cr isotope variations within Earth's silicate reservoirs. Further and more detailed studies are required to investigate whether silicate

  19. A thirty second isomer in Hf-171

    NARCIS (Netherlands)

    Campbell, P; Billowes, J; Cochrane, ECA; Cooke, JL; Cooper, TG; Dendooven, P; Evans, DE; Grant, IS; Griffith, JAR; Honkanen, A; Huhta, M; Oinonen, M; Pearson, MR; Penttila, H; Persson, B.L.; Richardson, DS; Tungate, G; Wheeler, PD; Zybert, L; Aysto, J


    An isomer has been detected in Hf-171 with a half-life of T-1/2 = 29.5(9) s. The state was populated in the Yb-170(alpha,3n)Hf-171m reaction at a beam energy of E-alpha = 50 MeV in an on-line ion guide isotope separator. The isomeric Hf-17lm(+) beam was extracted from the ion guide, mass-analysed an

  20. Geochemistry, geochronology and zircon Hf isotopic study of peralkaline-alkaline intrusions along the northern margin of the North China Craton and its tectonic implication for the southeastern Central Asian Orogenic Belt (United States)

    Zhao, Pan; Jahn, Bor-ming; Xu, Bei; Liao, Wen; Wang, Yanyang


    A giant Permian alkaline magmatic belt has recently been identified in southern Inner Mongolia, along the northern margin of the North China Craton (NCC). This belt is mainly composed of syenite, quartz syenite, alkaline granite and mafic microgranular enclaves (MME)-bearing granodiorite. In order to study the petrogenesis and tectonic implications of these rocks, we undertook zircon U-Pb dating and geochemical analysis of two Permian alkaline plutons. The first Guangxingyuan Pluton occurs in the Hexigten area and is composed of MME-bearing tonalite, K-feldspar granite and syenite. The second Durenwuliji Pluton, located in the Xianghuangqi area, comprises syenite, quartz syenite and K-feldspar granite. Zircon U-Pb dating on tonalite, K-feldspar granite, syenite and quartz syenite from the two plutons yielded a tight range of ages from 259 to 267 Ma. The peralkaline-alkaline rocks show high abundance of total alkalis (K2O + Na2O = 7.9-12.9%) and K2O contents (3.9-8.0%), enrichment in large ion lithophile elements (LILE) and light rare earth element (LREE), and depletion of high field strength elements (HFSE). The associated tonalite and MMEs display I-type granitic geochemical affinity, with less total abundance of trace elements than the peralkaline-alkaline rocks. Zircon Hf isotopic analysis of the Guangxingyuan pluton yielded a large range of εHf(t) values from - 15.5 to + 6.7 and model ages (TDMC) from 781 to 2012 Ma. By contrast, the Hf isotopic data of the Durenwuliji pluton shows a small range of εHf(t) from + 6.2 to + 8.9 and TDMC from 667 to 816 Ma. The geochemical and Hf isotopic characteristics indicate that the parental magma was derived from a mixing of metasomatic mantle-derived mafic magma with different amount of crust-derived felsic magma, and followed by fractional crystallization. Considering previous tectonic studies in Inner Mongolia, a Permian post-orogenic extension was proposed to account for these peralkaline-alkaline intrusions following

  1. The effect of small scale variablity in isotopic composition of precipitation on hydrograph separation results (United States)

    Fischer, Benjamin; van Meerveld, Ilja; Seibert, Jan


    Understanding runoff processes is important for predictions of streamflow quantity and quality. The two-component isotope hydrograph separation (IHS) method is a valuable tool to study how catchments transform rainfall into runoff. IHS allows the stormflow hydrograph to be separated into rainfall (event water) and water that was stored in the catchment before the event (pre-event water). To be able to perform an IHS, water samples of baseflow (pre-event water) and stormflow are collected at the stream outlet. Rainfall is usually collected at one location by hand as an event total or sampled sequentially during the event. It is usually assumed that the spatial variability in rainfall and the isotopic composition of rainfall are negligible for small (area of 0.15, 0.23, and 0.7 km2). The isotopic composition of rainfall and streamflow were sampled for 10 different rain events (P: 5 mm intervals, Q: 12 to 51 samples per events). This dataset was used to perform a two-component isotope hydrograph separation. The results show that for some events the spatial variability in total rainfall, mean and maximum rainfall intensity and stable isotope composition of rainfall was high. There was no relation between the stable isotope composition of rainfall and the rainfall sum, rainfall intensity or altitude. The spatial variability of the isotopic composition of rainfall was for 4 out of the 10 events as large as the temporal variability in the isotopic composition. Different rainfall weighing methods resulted in different minimum pre-event water fractions in streamflow. For small events with a small mean temporal range in stable isotope composition of rainfall, the different rainfall weighing methods had little effect on the calculated minimum pre-event water fractions. However with increasing temporal variability in stable isotope composition of rainfall, the range in the minimum pre-event water fractions increased and therefore the choice of the rainfall weighing method

  2. Chromium isotope composition of reducing and anoxic sediments from the Peru Margin and Cariaco Basin (United States)

    Gueguen, B.; Planavsky, N.; Wang, X.; Algeo, T. J.; Peterson, L. C.; Reinhard, C. T.


    Chromium isotope systematics in marine sediments are now being used as a new redox proxy of the modern and ancient Earth's surface. Chromium is primarily delivered to the oceans by riverine inputs through weathering of Cr(III)-rich minerals present in the continental crust and oxidation of insoluble Cr(III) to soluble Cr(VI) species. Since oxidation-reduction reactions fractionate Cr isotopes whereby oxidized Cr(VI) species are preferentially enriched in heavy Cr isotopes, the Cr isotope composition of marine sediments may be useful tracers of redox conditions at the Earth's surface through geological time. Chromium is quantitatively removed in organic-rich sediments where reducing conditions prevail and promote reduction of Cr(VI) to Cr(III), and thus, these sediments should capture the ambient seawater Cr isotope composition. However, the isotopic composition of modern organic-rich sediments is poorly documented so far, and this step is essential for further modeling the global oceanic Cr isotope mass balance and assessing the effects of sedimentation and post-depositional processes on the marine Cr isotopes archive. In this study, we have characterized modern marine organic-rich sediments for their Cr isotope composition (δ53/52Cr) from two different settings, the Peru margin upwelling zone and the anoxic Cariaco Basin (Venezuela). Chromium isotopes were measured on a MC-ICP-MS (Nu Plasma) using a double-spike correction method. The authigenic fraction of shallow samples from the Peru margin sedimentary sequence with a high Total Organic Carbon (TOC) content (>10 wt%) yield an average δ53/52Crauthigenic value of +0.67 ±0.05 ‰ (2sd). However, although this value is close to the seawater value (Atlantic Ocean) and to Cariaco basin sediments (~ +0.6 ‰), reducing sediments from the Peru margin are on average isotopically slightly heavier, especially in samples having a low authigenic fraction and a low TOC content (δ53/52Crauthigenic values up to +1.30

  3. In situ zircon Hf isotopic, U-Pb age and trace element study of monzonite xenoliths from Pingquan and Fuxin basalts: Tracking the thermal events of 169 Ma and 107 Ma in Yanliao area

    Institute of Scientific and Technical Information of China (English)

    ZHENG; Jianping; ZHANG; Ruisheng; YU; Chunmei; TANG; Huay


    K-Ar ages of the Mesozoic (92-100 Ma) Fuxin alkalic basalts (western Liaoning Province) and the Tertiary (23-45 Ma) Pingquan alkalic basalts (eastern Hebei Province), and the results of in situ zircon U-Pb dating, Hf isotope and the trace elements from three monzonite xenoliths carried in the alkalic basalts are reported. The crust-mantle interaction occurring in the Yanshan intracontinental orogenic belt is also discussed. Fuxin zircons show highly uniform U-Pb age ((169±3) Ma). More than 95% Pingquan zircons display the age of (107±10) Ma except two are 2491 Ma and 513 Ma respectively. Zircons with the ages of (169±3) Ma have εHf close to zero. εHf of the zircons with the ages of (107±10) Ma are mainly at -11.5--16.3, showing the crustal derivation. Fuxin zircons contain low Nb, Ta, Sr, Th, U contents, low and narrow Hf model ages (0.87-1.00 Ga), which reflect that the source materials of the monzonite xenoliths are young to Pingquan (focus at (1.28±0.08) Ga). High contents of the incompatible elements, and wide range of Hf model ages (0.89-2.56 Ga) in Pingquan zircons suggest a more complex source and the highly crustal maturity in their petrogenesis. Comprehensive information including the published data indicates that J3-K1 is the key period of the deep processes and shallow tectonic reverse in the Yanliao area. However, the processes were highly heterogeneous in spatial and in temporal.

  4. In situ zircon Hf isotopic, U-Pb age and trace element study of monzonite xenoliths from Pingquan and Fuxin basalts:Tracking the thermal events of 169 Ma and 107 Ma in Yanliao area

    Institute of Scientific and Technical Information of China (English)

    ZHENG Jianping; ZHANG Ruisheng; YU Chunmei; TANG Huayun; ZHANG Pei


    K-Ar ages of the Mesozoic (92-100 Ma) Fuxin alkalic basalts (western Liaoning Province) and the Tertiary (23-45 Ma) Pingquan alkalic basalts (eastern Hebei Province), and the results of in situ zircon U-Pb dating, Hf isotope and the trace elements from three monzonite xenoliths carried in the alkalic basalts are reported. The crust-mantle interaction occurring in the Yanshan intracontinental orogenic belt is also discussed. Fuxin zircons show highly uniform U-Pb age ((169±3) Ma). More than 95% Pingquan zircons display the age of (107±10) Ma except two are 2491 Ma and 513 Ma respectively. Zircons with the ages of (169±3) Ma have εHf close to zero. εHf of the zircons with the ages of (107±10) Ma are mainly at -11.5--16.3, showing the crustal derivation. Fuxin zircons contain low Nb, Ta, Sr, Th, U contents, low and narrow Hf model ages (0.87-1.00 Ga), which reflect that the source materials of the monzonite xenoliths are young to Pingquan (focus at (1.28±0.08) Ga). High contents of the incompatible elements, and wide range of Hf model ages (0.89-2.56 Ga) in Pingquan zircons suggest a more complex source and the highly crustal maturity in their petrogenesis. Comprehensive information including the published data indicates that J3-K1 is the key period of the deep processes and shallow tectonic reverse in the Yanliao area. However, the processes were highly heterogeneous in spatial and in temporal.

  5. Hf-W chronometry of core formation in planetesimals inferred from weakly irradiated iron meteorites (United States)

    Kruijer, Thomas S.; Sprung, Peter; Kleine, Thorsten; Leya, Ingo; Burkhardt, Christoph; Wieler, Rainer


    The application of Hf-W chronometry to determine the timescales of core formation in the parent bodies of magmatic iron meteorites is severely hampered by 182W burnout during cosmic ray exposure of the parent meteoroids. Currently, no direct method exists to correct for the effects of 182W burnout, making the Hf-W ages for iron meteorites uncertain. Here we present noble gas and Hf-W isotope systematics of iron meteorite samples whose W isotopic compositions remained essentially unaffected by cosmic ray interactions. Most selected samples have concentrations of cosmogenic noble gases at or near the lowermost level observed in iron meteorites and, for iron meteorite standards, have very low noble gas and radionuclide based cosmic ray exposure ages (Mbosi), however, has elevated ɛ182W relative to the other investigated irons, indicating metal-silicate separation ˜2-3 Myr later than in the parent bodies of the three major iron meteorite groups studied here.

  6. The isotopic composition of dissolved cadmium in the water column of the West Philippine Sea

    Directory of Open Access Journals (Sweden)

    Shun-Chung eYang


    Full Text Available The dissolved concentration and isotopic compositions of cadmium (Cd in the seawater of the West Philippine Sea were determined. In general, Cd isotopic composition in the water column decreased with depth, with ε114/110Cd (ε114/110Cd = [(114Cd/110Cdsample / (114Cd/110CdNIST 3108 - 1]×10000 ranging from +7.2 to +10.1 in the top 60 m, from +4.8 to +5.1 between 100 and 150 m, peaking at +8.2 at 200 m, decreasing from +4.5 to +3.3 from 400 to 1000 m, and remaining constant at +3.0 from 1000 m and deeper. Different to a Rayleigh fractionation model, the isotopic composition and log scale concentrations of Cd do not exhibit a linear relationship. However, from the deep water to thermocline, the variations in Cd concentration and ε114/110Cd are relevant to the variations of temperature and salinity, indicating that water mixing is the dominant processes determining the concentration and isotopic composition in the interval. At 200 m where North Pacific Tropic Water dominates the water mass, the elevated ε114/110Cd could be linked to the composition in the upper portions of the water mass. In the top 150 m, the ε114/110Cd varies similarly to the phytoplankton community structures, implying that Cd uptake by various phytoplankton species may be associated with the isotopic variation. However, the effects of atmospheric inputs to the ε114/110Cd in the surface water cannot be excluded. A box model calculation is used to constrain the contributions of various processes to the Cd isotopes of surface water, and the results indicate that the Cd concentration and isotopic composition in most of the water body of the region are controlled by physical mixing, while the effects of biological fractionation and atmospheric inputs are limited in the euphotic zone.

  7. The minor sulfur isotope composition of Cretaceous and Cenozoic seawater sulfate (United States)

    Masterson, A. L.; Wing, Boswell A.; Paytan, Adina; Farquhar, James; Johnston, David T.


    The last 125 Myr capture major changes in the chemical composition of the ocean and associated geochemical and biogeochemical cycling. The sulfur isotopic composition of seawater sulfate, as proxied in marine barite, is one of the more perplexing geochemical records through this interval. Numerous analytical and geochemical modeling approaches have targeted this record. In this study we extend the empirical isotope record of seawater sulfate to therefore include the two minor sulfur isotopes, 33S and 36S. These data record a distribution of values around means of Δ33S and Δ36S of 0.043 ± 0.016‰ and -0.39 ± 0.15‰, which regardless of δ34S-based binning strategy is consistent with a signal population of values throughout this interval. We demonstrate with simple box modeling that substantial changes in pyrite burial and evaporite sulfate weathering can be accommodated within the range of our observed isotopic values.

  8. The atomic weight and isotopic composition of nitrogen and their variation in nature

    Energy Technology Data Exchange (ETDEWEB)

    Holden, N.E.


    Two stable isotopes of nitrogen exist in nature, /sup 14/N and /sup 15/N. The less abundant isotope, /sup 15/N, was discovered in 1929 by Naude, who studied the band spectra of nitric oxide, NO. However, the main source of a standard for this element is the air in the atmosphere, which is made up of approximately 78% N/sub 2/. Reviewed in this paper is the measurements of the isotopic composition in air and its variation around the world. Also investigated is the variation of the isotopic composition in the various compounds or sources of nitrogen compared to the value in air. Data on the atomic weight and non-terrestrial data for nitrogen is also reviewed.

  9. On the isotopic composition of precipitation; Sur la composition isotopique des precipitations

    Energy Technology Data Exchange (ETDEWEB)

    Gonfiantini, R. [Paris-11 Univ., 91 - Orsay (France). Laboratoire d`Hydrologie et de Geochimie Isotopique


    The paper discusses some aspects of the isotopic composition (tritium and stable isotopes) of global precipitation which is being monitored since the late fifties through the network established by the International Atomic Energy Agency. Three quarters of the tritium formed during the atmospheric thermonuclear tests were released in the biennium 1961-1962. The successive five years of the test moratorium provide a unique information on the tritium transfer rate from the stratosphere to the troposphere. The tritium concentration decreased steadily, and the decrease rate appears to be greater at high latitude. This fact can possibly be explained by precipitation recycling by evapotranspiration, which is more important at low latitudes, and tritium concentration ratio between two successive years, is close to 0.68 {+-} 0.02, with the exception of the year 1965, when the tritium content dropped to 0.50 {+-} 0.02 with respect to the previous year. At latitudes between 30 and 60 deg C, the correlations between {delta}{sup 2}H and {delta}{sup 18}O show almost identical slopes in winter and summer precipitation, but different intercepts. The correlations are: {delta}{sup 2}H (8.36{+-}0.13) {delta}{sup 18}O+(14.2{+-}4.2) for January and {delta}{sup 2}H 8.33{+-}0.013) {delta}{sup 18}O+(8.2{+-}3.9) for July. This reflects a different seasonal deuterium excess (defined as d {delta}{sup 2}H - 8{delta}{sup 18}O), which has a mean value of 10.7{+-} 0.6 %0 in July, and a higher average value of 10.7 {+-} 0.6%0 in January and 5.8{+-} 0.5%0 in July, and a higher average value in stations with prevailing winter rains. Also, the slope becomes about 8 when summer and winter precipitation are considered all together. The altitude effect on the isotopic composition of precipitation on Mount Cameroon is re-examined. The model which best fits the data is based on the adiabatic condensation of the atmospheric vapour with a liquid/vapor ratio increasing from 0.15 at sea level to 0.45 at 4

  10. Natural variations in the rhenium isotopic composition of meteorites (United States)

    Liu, R.; Hu, L.; Humayun, M.


    Rhenium is an important element with which to test hypotheses of isotope variation. Historically, it has been difficult to precisely correct the instrumental mass bias in thermal ionization mass spectrometry. We used W as an internal standard to correct mass bias on the MC-ICP-MS, and obtained the first precise δ187Re values ( ±0.02‰, 2SE) for iron meteorites and chondritic metal. Relative to metal from H chondrites, IVB irons are systematically higher in δ187Re by 0.14 ‰. δ187Re for other irons are similar to H chondritic metal, although some individual samples show significant isotope fractionation. Since 185Re has a high neutron capture cross section, the effect of galactic cosmic-ray (GCR) irradiation on δ187Re was examined using correlations with Pt isotopes. The pre-GCR irradiation δ187Re for IVB irons is lower, but the difference in δ187Re between IVB irons and other meteoritic metal remains. Nuclear volume-dependent fractionation for Re is about the right magnitude near the melting point of iron, but because of the refractory and compatible character of Re, a compelling explanation in terms of mass-dependent fractionation is elusive. The magnitude of a nucleosynthetic s-process deficit for Re estimated from Mo and Ru isotopes is essentially unresolvable. Since thermal processing reduced nucleosynthetic effects in Pd, it is conceivable that Re isotopic variations larger than those in Mo and Ru may be present in IVBs since Re is more refractory than Mo and Ru. Thus, the Re isotopic difference between IVBs and other irons or chondritic metal remains unexplained.

  11. Variation in the terrestrial isotopic composition and atomic weight of argon (United States)

    Böhlke, John Karl


    The isotopic composition and atomic weight of argon (Ar) are variable in terrestrial materials. Those variations are a source of uncertainty in the assignment of standard properties for Ar, but they provide useful information in many areas of science. Variations in the stable isotopic composition and atomic weight of Ar are caused by several different processes, including (1) isotope production from other elements by radioactive decay (radiogenic isotopes) or other nuclear transformations (e.g., nucleogenic isotopes), and (2) isotopic fractionation by physical-chemical processes such as diffusion or phase equilibria. Physical-chemical processes cause correlated mass-dependent variations in the Ar isotope-amount ratios (40Ar/36Ar, 38Ar/36Ar), whereas nuclear transformation processes cause non-mass-dependent variations. While atmospheric Ar can serve as an abundant and homogeneous isotopic reference, deviations from the atmospheric isotopic ratios in other Ar occurrences limit the precision with which a standard atomic weight can be given for Ar. Published data indicate variation of Ar atomic weights in normal terrestrial materials between about 39.7931 and 39.9624. The upper bound of this interval is given by the atomic mass of 40Ar, as some samples contain almost pure radiogenic 40Ar. The lower bound is derived from analyses of pitchblende (uranium mineral) containing large amounts of nucleogenic 36Ar and 38Ar. Within this interval, measurements of different isotope ratios (40Ar/36Ar or 38Ar/36Ar) at various levels of precision are widely used for studies in geochronology, water–rock interaction, atmospheric evolution, and other fields.

  12. Molybdenum isotopic composition of single silicon carbides from supernovae.

    Energy Technology Data Exchange (ETDEWEB)

    Amari, S.; Clayton, R. N.; Davis, A. M.; Lewis, R. S.; Pellin, M. J.


    Presolar silicon carbide grains form in a variety of types of stars, including asymptotic giant branch red giant stars and supernovae. The dominant mechanisms of heavy element nucleosynthesis, the s-process and r-process, are thought to occur in AGB stars and supernovae, respectively. We have previously reported that mainstream SiC grains have strong enrichments in the s-process isotopes of Sr, Zr and Mo. We report here the first measurements of Mo isotopes in X-type SiC grains, which have previously been identified as having formed from supernova ejecta.

  13. Composition-driven phase boundary and electrical properties in (Ba₀.₉₄Ca₀.₀₆)(Ti₁-xMx)O₃ (M = Sn, Hf, Zr) lead-free ceramics. (United States)

    Zhao, Chunlin; Wang, Hui; Xiong, Jie; Wu, Jiagang


    In this study, we systematically investigated the composition dependence of the phase structure, microstructure, and electrical properties of (Ba0.94Ca0.06)(Ti1-xMx)O3 (M = Sn, Hf, Zr) ceramics synthesised by the conventional solid-state reaction method. The phase boundary type strongly depends on the composition, and then different electrical properties were exhibited. The addition of Hf and Zr can more quickly shift phase transition temperatures (TR-O and TO-T) to a higher temperature with respect to Sn, leading to the formation of different phase boundaries. In addition, different phase boundaries can also be affected by their doped contents. The R-O and O-T phase boundaries can be shown in the Sn-doped ceramics with x = 0.10, and the R-O phase boundary can exist in the Hf (x = 0.07) or Zr (x = 0.075)-doped ceramics. A high piezoelectric property of d33 = 600 pC N(-1) can be achieved in the Sn-doped ceramics due to the involvement of converging R-O/O-T phase boundaries, an enhanced ferroelectric performance with Pr = 14.54 μC cm(-2) and Ec = 1.82 kV cm(-1) can be attained in the Zr-doped ceramics, and Hf would benefit from obtaining a large strain behaviour (∼0.20%). We believe that the electrical properties and the related physical mechanisms of BaTiO3-based ceramics can be well unveiled by studying their chemical modification behavior.

  14. Is my C isotope excursion global, local, or both? Insights from the Mg and Ca isotopic composition of primary, diagenetic, and authigenic carbonates (United States)

    Higgins, J. A.; Blättler, C. L.; Husson, J. M.


    The C isotopic composition of ancient limestones and dolomites is a widely used proxy for the global geochemical cycles of carbon and oxygen in the ocean-atmosphere system and a critical tool for chemostratigraphy in Precambrian rocks. Although relatively robust to diagenesis, the C isotopic composition of bulk carbonates can be reset when conditions favor high water-to-rock ratios or fluids with high C concentrations and distinct isotopic compositions. Authigenic carbonates and different pools of primary carbonate (e.g. calcite vs. aragonite) may also bias the C isotopic composition of bulk carbonates if they are both abundant and isotopically distinct. New approaches to quantifying contributions from diagenesis, authigenesis, and mixing of primary carbonates to the C isotopic composition of bulk sedimentary carbonates are needed. Here we present preliminary Mg and Ca isotope data sets of primary, diagenetic, and authigenic carbonates, both modern and ancient. We show that recrystallization, dolomitization, and authigenesis produce Mg and Ca isotope fingerprints that may be used to identify and characterize these processes in ancient carbonate sediments.

  15. Hafnium at subduction zones: isotopic budget of input and output fluxes; L'hafnium dans les zones de subduction: bilan isotopique des flux entrant et sortant

    Energy Technology Data Exchange (ETDEWEB)

    Marini, J.Ch


    Subduction zones are the primary regions of mass exchanges between continental crust and mantle of Earth through sediment subduction toward the earth's mantle and by supply of mantellic magmas to volcanic arcs. We analyze these mass exchanges using Hafnium and Neodymium isotopes. At the Izu-Mariana subduction zone, subducting sediments have Hf and Nd isotopes equivalent to Pacific seawater. Altered oceanic crust has Hf and Nd isotopic compositions equivalent to the isotopic budget of unaltered Pacific oceanic crust. At Luzon and Java subduction zones, arc lavas present Hf isotopic ratios highly radiogenic in comparison to their Nd isotopic ratios. Such compositions of the Luzon and Java arc lavas are controlled by a contamination of their sources by the subducted oceanic sediments. (author)

  16. Potassium Isotopic Compositions of NIST Potassium Standards and 40Ar/39Ar Mineral Standards (United States)

    Morgan, Leah; Tappa, Mike; Ellam, Rob; Mark, Darren; Higgins, John; Simon, Justin I.


    Knowledge of the isotopic ratios of standards, spikes, and reference materials is fundamental to the accuracy of many geochronological methods. For example, the 238U/235U ratio relevant to U-Pb geochronology was recently re-determined [1] and shown to differ significantly from the previously accepted value employed during age determinations. These underlying values are fundamental to accurate age calculations in many isotopic systems, and uncertainty in these values can represent a significant (and often unrecognized) portion of the uncertainty budget for determined ages. The potassium isotopic composition of mineral standards, or neutron flux monitors, is a critical, but often overlooked component in the calculation of K-Ar and 40Ar/39Ar ages. It is currently assumed that all terrestrial materials have abundances indistinguishable from that of NIST SRM 985 [2]; this is apparently a reasonable assumption at the 0.25per mille level (1s) [3]. The 40Ar/39Ar method further relies on the assumption that standards and samples (including primary and secondary standards) have indistinguishable 40K/39K values. We will present data establishing the potassium isotopic compositions of NIST isotopic K SRM 985, elemental K SRM 999b, and 40Ar/39Ar biotite mineral standard GA1550 (sample MD-2). Stable isotopic compositions (41K/39K) were measured by the peak shoulder method with high resolution MC-ICP-MS (Thermo Scientific NEPTUNE Plus), using the accepted value of NIST isotopic SRM 985 [2] for fractionation [4] corrections [5]. 40K abundances were measured by TIMS (Thermo Scientific TRITON), using 41K/39K values from ICP-MS measurements (or, for SRM 985, values from [2]) for internal fractionation corrections. Collectively these data represent an important step towards a metrologically traceable calibration of 40K concentrations in primary 40Ar/39Ar mineral standards and improve uncertainties by ca. an order of magnitude in the potassium isotopic compositions of standards.

  17. About the possibility of creating a continuous range of standards with different isotopic composition of carbon

    Directory of Open Access Journals (Sweden)

    S. A. Sadykov


    Full Text Available It is established that the carbon isotopic composition in the formation of calcium carbonate is changed depending on the magnetic field strength. The formation of calcium carbonate occurred due to the interaction of calcium hydroxide with atmospheric carbon dioxide. The profile of isotopic relations13C/12C of the newly formed calcium carbonate is approximated by the equation of the parabola for certain values of tension solenoidal magnetic field. The possibility of creating standards with a continuous series of values of the content of carbon stable isotopes based on the data suggested.

  18. The isotopic composition of dissolved inorganic nitrogen in hydrothermal vent fluids (United States)

    Lehmann, M. F.; Bourbonnais, A.; Butterfield, D. A.


    Hydrothermal vent systems at mid-ocean ridges are sites with rapid rates of biomass production, sustained by chemolithoautotrophic bacteria at the base of the vent community food chains. The exact metabolic pathways, in particular those that involve nitrogen (N), and the rates at which the metabolic reactions take place are poorly constrained. In previous studies, very low 15N/14N ratios have been attributed to strong N isotope fractionation during chemosynthetic assimilation of ammonium. However, actual data on the N isotopic composition of dissolved inorganic N in vent systems, which could provide coherent information on the sources of N during chemolithoautotrophic biosynthesis, do not exist. Furthermore, the fate of hydrothermally discharged ammonium as well as that of nitrate that is mixed in from the ocean water column have not been the focus of much attention. As a consequence, little is known about N-cycle reactions within hydrothermal vent systems. We will present nitrate isotope (15N/14N and 18O/16O) data from various sites at Axial Volcano on the Juan de Fuca ridge. Their integration with nitrate concentration data suggests non-conservative behavior of nitrate along temperature gradients. Highest N and O isotope ratios (7.6 permil and 21.0 permil, respectively) are found in average diffuse fluids (17°C). Elevated N and O isotope ratios were associated with decreased nitrate concentrations and indicate a nitrate consuming process that fractionates both N and O isotopes. The ratio of 15N versus 18O enrichment in residual nitrate is, however, not consistent with previous reports on nitrate N versus O isotope fractionation during denitrification in the suboxic ocean water column, implying anomalous N and O isotope fractionation during denitrification in hydrothermal vent fluids and/or the presence of additional microbially mediated N transformations that affect the N and O isotope composition of the nitrate pool in the Axial hydrothermal vent system in a

  19. Zirconium isotope constraints on the composition of Theia and current Moon-forming theories (United States)

    Akram, W.; Schönbächler, M.


    The giant impact theory is the most widely recognized formation scenario of the Earth's Moon. Giant impact models based on dynamical simulations predict that the Moon acquired a significant amount of impactor (Theia) material, which is challenging to reconcile with geochemical data for O, Si, Cr, Ti and W isotopes in the Earth and Moon. Three new giant impact scenarios have been proposed to account for this discrepancy - hit-and-run impact, impact with a fast-spinning protoEarth and massive impactors - each one reducing the proportion of the impactor in the Moon compared to the original canonical giant impact model. The validity of each theory and their different dynamical varieties are evaluated here using an integrated approach that considers new high-precision Zr isotope measurements of lunar rocks, and quantitative geochemical modelling of the isotopic composition of the impactor Theia. All analysed lunar samples (whole-rock, ilmenite and pyroxene separates) display identical Zr isotope compositions to that of the Earth within the uncertainty of 13 ppm for 96Zr/90Zr (2σ weighted average). This 13 ppm upper limit is used to infer the most extreme isotopic composition that Theia could have possessed, relative to the Earth, for each of the proposed giant impact theories. The calculated Theian composition is compared with the Zr isotope compositions of different solar system materials in order to constrain the source region of the impactor. As a first order approximation, we show that all considered models (including the canonical) are plausible, alleviating the initial requirement for the new giant impact models. Albeit, the canonical and hit-and-run models are the most restrictive, suggesting that the impactor originated from a region close to the Earth. The fast-spinning protoEarth and massive impactor models are more relaxed and increase the allowed impactor distance from the Earth. Similar calculations carried out for O, Cr, Ti and Si isotope data support

  20. Water transport in protoplanetary disks and the hydrogen isotopic composition of chondrites

    CERN Document Server

    Jacquet, Emmanuel


    The D/H ratios of carbonaceous chondrites, believed to reflect that of water in the inner early solar system, are intermediate between the protosolar value and that of most comets. The isotopic composition of cometary water has been accounted for by several models where the isotopic composition of water vapor evolved by isotopic exchange with hydrogen gas in the protoplanetary disk. However, the position and the wide variations of the distribution of D/H ratios in carbonaceous chondrites have yet to be explained. In this paper, we assume that the D/H composition of cometary ice was achieved in the disk building phase and model the further isotopic evolution of water in the inner disk in the classical T Tauri stage. Reaction kinetics compel isotopic exchange between water and hydrogen gas to stop at $\\sim$500 K, but equilibrated water can be transported to the snow line (and beyond) via turbulent diffusion and consequently mix with isotopically comet-like water. Under certain simplifying assumptions, we calcul...


    Poitrasson, F.; Zambardi, T.; Magna, T.; Neal, C. R.


    It is difficult to estimate the bulk chemical and isotopic properties of planets, especially for the Moon for which our sampling is far more limited than for the Earth. As a result, there is currently a debate on the bulk Fe isotope composition of the Moon: Whereas in a first study we proposed that the bulk lunar Fe isotope composition (δ57Fe ~0.2‰) was twice as heavy as that of the Earth (δ57Fe ~0.1‰) relative to chondrites (δ57Fe ~0‰), normalized to IRMM-14, others proposed that there is no difference between Earth and Moon. This question is of crucial importance because the first case may track the Moon-forming giant interplanetary impact, whereas the alternative situation may also result from a very high pressure metal-silicate fractionation during the Earth’s core formation, assuming that the Moon subsequently inherited the Earth Fe isotope composition. To reassess this question, we analyzed a suite of 18 mare basalts (both high- and low-Ti) by MC-ICP-MS using the nickel doping technique developed at LMTG. Combined with our previous measurements of lunar rocks, we obtained a mean δ57Fe of 0.138±0.035‰ (2SE, n=11) for low-Ti basalts, 0.269±0.026‰ (2SE, n=16) for high-Ti ones and 0.177±0.036‰ (2SE, n=6) for highland rocks. T-tests confirm that averages of low- and high-Ti basalts are significantly different at the 95% confidence level. Similarly, t-tests indicate that highland rocks are significantly different from high-Ti basalts, but not from low-Ti ones. These new data therefore confirm suggestion from previous groups that low- and high-Ti basalts contain distinct Fe isotope signatures. This shows that on the Moon, high temperature processes can significantly change the Fe isotope composition of bulk mafic rocks at the planetary scale. This cannot result from simple equilibrium magmatic fractionation or assimilation of ilmenite given its Fe isotope fractionation factor, however. We conclude that another process, yet to be identified, is

  2. Thallium-isotopic compositions of euxinic sediments as a proxy for global manganese-oxide burial (United States)

    Owens, Jeremy D.; Nielsen, Sune G.; Horner, Tristan J.; Ostrander, Chadlin M.; Peterson, Larry C.


    Thallium (Tl) isotopes are a new and potentially powerful paleoredox proxy that may track bottom water oxygen conditions based on the global burial flux of manganese oxides. Thallium has a residence time of ∼20 thousand years, which is longer than the ocean mixing time, and it has been inferred that modern oxic seawater is conservative with respect to both concentration and isotopes. Marine sources of Tl have nearly identical isotopic values. Therefore, the Tl sinks, adsorption onto manganese oxides and low temperature oceanic crust alteration (the dominant seawater output), are the primary controls of the seawater isotopic composition. For relatively short-term, ∼million years, redox events it is reasonable to assume that the dominant mechanism that alters the Tl isotopic composition of seawater is associated with manganese oxide burial because large variability in low temperature ocean crust alteration is controlled by long-term, multi-million years, average ocean crust production rates. This study presents new Tl isotope data for an open ocean transect in the South Atlantic, and depth transects for two euxinic basins (anoxic and free sulfide in the water column), the Cariaco Basin and Black Sea. The Tl isotopic signature of open ocean seawater in the South Atlantic was found to be homogeneous with ε205Tl = -6.0 ± 0.3 (±2 SD, n = 41) while oxic waters from Cariaco and the Black Sea are -5.6 and -2.2, respectively. Combined with existing data from the Pacific and Arctic Oceans, our Atlantic data establish the conservatism of Tl isotopes in the global ocean. In contrast, partially- and predominantly-restricted basins reveal Tl isotope differences that vary between open-ocean (-6) and continental material (-2) ε205Tl, scaling with the degree of restriction. Regardless of the differences between basins, Tl is quantitatively removed from their euxinic waters below the chemocline. The burial of Tl in euxinic sediments is estimated to be an order of magnitude

  3. The oxygen isotopic composition of the Sun inferred from captured solar wind. (United States)

    McKeegan, K D; Kallio, A P A; Heber, V S; Jarzebinski, G; Mao, P H; Coath, C D; Kunihiro, T; Wiens, R C; Nordholt, J E; Moses, R W; Reisenfeld, D B; Jurewicz, A J G; Burnett, D S


    All planetary materials sampled thus far vary in their relative abundance of the major isotope of oxygen, (16)O, such that it has not been possible to define a primordial solar system composition. We measured the oxygen isotopic composition of solar wind captured and returned to Earth by NASA's Genesis mission. Our results demonstrate that the Sun is highly enriched in (16)O relative to the Earth, Moon, Mars, and bulk meteorites. Because the solar photosphere preserves the average isotopic composition of the solar system for elements heavier than lithium, we conclude that essentially all rocky materials in the inner solar system were enriched in (17)O and (18)O, relative to (16)O, by ~7%, probably via non-mass-dependent chemistry before accretion of the first planetesimals.

  4. Zinc isotope fractionation during mantle melting and constraints on the Zn isotope composition of Earth's upper mantle (United States)

    Wang, Ze-Zhou; Liu, Sheng-Ao; Liu, Jingao; Huang, Jian; Xiao, Yan; Chu, Zhu-Yin; Zhao, Xin-Miao; Tang, Limei


    compositions of MORB. Therefore, preferential melting of spinel in the peridotites may account for the Zn isotopic difference between spinel peridotites and basalts. By contrast, the absence of Zn isotope fractionation between silicate minerals suggests that Zn isotopes are not significantly fractionated during partial melting of spinel-free garnet-facies mantle. If the studied non-metasomatized peridotites represent the refractory upper mantle, mass balance calculation shows that the depleted MORB mantle (DMM) has a δ66Zn value of +0.20 ± 0.05‰ (2SD), which is lighter than the primitive upper mantle (PUM) estimated in previous studies (+0.28 ± 0.05‰, 2SD, Chen et al., 2013b; +0.30 ± 0.07‰, 2SD, Doucet et al., 2016). This indicates that the Earth's upper mantle has a heterogeneous Zn isotopic composition vertically, which is probably due to shallow mantle melting processes.

  5. Variation in the Carbon Isotope Compositions of Phytoliths Across a Climate Gradient (United States)

    Webb, E. A.; Longstaffe, F. J.


    The carbon isotope composition of plant organic matter within a single species may vary in response to changes in temperature, relative humidity, precipitation amount, altitude, nutrient availability, light levels and amount of canopy. All of these factors affect the rate of carbon assimilation during photosynthesis. Silica phytoliths, which form in the cells and intercellular spaces of terrestrial plants, occlude some of the plant's organic matrix. Carbon sequestered in phytoliths is protected from decay and may therefore be preserved in soils after most other plant material has decomposed. The carbon isotope composition of phytoliths may therefore have potential as an archive of climatic conditions during soil accumulation. In this study, the carbon isotope compositions of modern plant tissues and their phytoliths are compared for the C4 grass species Calamovilfa longifolia across the climate gradient of the North American prairies. The carbon isotope compositions of C. longifolia tissues ranged from -15 to -10 permil, with lower values being most typical of leaf tissues and with greater variability occurring in samples from lower latitudes. Carbonaceous compounds occluded in the phytoliths, by comparison, were depleted of carbon-13 by 5 to 15 permil relative to the tissues from the same plant. Understanding the causes of this offset, which is significantly larger and more variable than reported in previous studies, is necessary before the full potential of the carbon-isotope phytolith proxy can be realized.

  6. SIMSISH technique does not alter the apparent isotopic composition of bacterial cells.

    Directory of Open Access Journals (Sweden)

    Olivier Chapleur

    Full Text Available In order to identify the function of uncultured microorganisms in their environment, the SIMSISH method, combining in situ hybridization (ISH and nanoscale secondary ion mass spectrometry (nanoSIMS imaging, has been proposed to determine the quantitative uptake of specific labelled substrates by uncultured microbes at the single cell level. This technique requires the hybridization of rRNA targeted halogenated DNA probes on fixed and permeabilized microorganisms. Exogenous atoms are introduced into cells and endogenous atoms removed during the experimental procedures. Consequently differences between the original and the apparent isotopic composition of cells may occur. In the present study, the influence of the experimental procedures of SIMSISH on the isotopic composition of carbon in E. coli cells was evaluated with nanoSIMS and compared to elemental analyser-isotopic ratio mass spectrometer (EA-IRMS measurements. Our results show that fixation and hybridization have a very limited, reproducible and homogeneous influence on the isotopic composition of cells. Thereby, the SIMSISH procedure minimizes the contamination of the sample by exogenous atoms, thus providing a means to detect the phylogenetic identity and to measure precisely the carbon isotopic composition at the single cell level. This technique was successfully applied to a complex sample with double bromine - iodine labelling targeting a large group of bacteria and a specific archaea to evaluate their specific (13C uptake during labelled methanol anaerobic degradation.

  7. SIMSISH technique does not alter the apparent isotopic composition of bacterial cells. (United States)

    Chapleur, Olivier; Wu, Ting-Di; Guerquin-Kern, Jean-Luc; Mazéas, Laurent; Bouchez, Théodore


    In order to identify the function of uncultured microorganisms in their environment, the SIMSISH method, combining in situ hybridization (ISH) and nanoscale secondary ion mass spectrometry (nanoSIMS) imaging, has been proposed to determine the quantitative uptake of specific labelled substrates by uncultured microbes at the single cell level. This technique requires the hybridization of rRNA targeted halogenated DNA probes on fixed and permeabilized microorganisms. Exogenous atoms are introduced into cells and endogenous atoms removed during the experimental procedures. Consequently differences between the original and the apparent isotopic composition of cells may occur. In the present study, the influence of the experimental procedures of SIMSISH on the isotopic composition of carbon in E. coli cells was evaluated with nanoSIMS and compared to elemental analyser-isotopic ratio mass spectrometer (EA-IRMS) measurements. Our results show that fixation and hybridization have a very limited, reproducible and homogeneous influence on the isotopic composition of cells. Thereby, the SIMSISH procedure minimizes the contamination of the sample by exogenous atoms, thus providing a means to detect the phylogenetic identity and to measure precisely the carbon isotopic composition at the single cell level. This technique was successfully applied to a complex sample with double bromine - iodine labelling targeting a large group of bacteria and a specific archaea to evaluate their specific (13)C uptake during labelled methanol anaerobic degradation.

  8. Spurious and functional correlates of the isotopic composition of a generalist across a tropical rainforest landscape

    Directory of Open Access Journals (Sweden)

    Poirson Evan K


    Full Text Available Abstract Background The isotopic composition of generalist consumers may be expected to vary in space as a consequence of spatial heterogeneity in isotope ratios, the abundance of resources, and competition. We aim to account for the spatial variation in the carbon and nitrogen isotopic composition of a generalized predatory species across a 500 ha. tropical rain forest landscape. We test competing models to account for relative influence of resources and competitors to the carbon and nitrogen isotopic enrichment of gypsy ants (Aphaenogaster araneoides, taking into account site-specific differences in baseline isotope ratios. Results We found that 75% of the variance in the fraction of 15N in the tissue of A. araneoides was accounted by one environmental parameter, the concentration of soil phosphorus. After taking into account landscape-scale variation in baseline resources, the most parsimonious model indicated that colony growth and leaf litter biomass accounted for nearly all of the variance in the δ15N discrimination factor, whereas the δ13C discrimination factor was most parsimoniously associated with colony size and the rate of leaf litter decomposition. There was no indication that competitor density or diversity accounted for spatial differences in the isotopic composition of gypsy ants. Conclusion Across a 500 ha. landscape, soil phosphorus accounted for spatial variation in baseline nitrogen isotope ratios. The δ15N discrimination factor of a higher order consumer in this food web was structured by bottom-up influences - the quantity and decomposition rate of leaf litter. Stable isotope studies on the trophic biology of consumers may benefit from explicit spatial design to account for edaphic properties that alter the baseline at fine spatial grains.

  9. The isotopic composition of methane in the stratosphere: high-altitude balloon sample measurements

    Directory of Open Access Journals (Sweden)

    T. Röckmann


    Full Text Available The isotopic composition of stratospheric methane has been determined on a large suite of air samples from stratospheric balloon flights covering subtropical to polar latitudes and a time period of 16 yr. 154 samples were analyzed for δ13C and 119 samples for δD, increasing the previously published dataset for balloon borne samples by an order of magnitude, and more than doubling the total available stratospheric data (including aircraft samples published to date. The samples also cover a large range in mixing ratio from tropospheric values near 1800 ppb down to only 250 ppb, and the strong isotope fractionation processes accordingly increase the isotopic composition up to δ13C = −14‰ and δD = +190‰, the largest enrichments observed for atmospheric CH4 so far. When analyzing and comparing kinetic isotope effects (KIEs derived from single balloon profiles, it is necessary to take into account the residence time in the stratosphere in combination with the observed mixing ratio and isotope trends in the troposphere, and the range of isotope values covered by the individual profile. The isotopic composition of CH4 in the stratosphere is affected by both chemical and dynamical processes. This severely hampers interpretation of the data in terms of the relative fractions of the three important sink mechanisms (reaction with OH, O(1D and Cl. It is shown that a formal sink partitioning using the measured data severely underestimates the fraction removed by OH, which is likely due to the insensitivity of the measurements to the kinetic fractionation in the lower stratosphere. Full quantitative interpretation of the CH4 isotope data in terms of the three sink reactions requires a global model.

  10. Hydrogen isotope composition of mantle-derived mica megacryst from ion micro probe analysis

    Institute of Scientific and Technical Information of China (English)

    夏群科; 陈道公; 支霞臣


    The hydrogen isotope composition of a mantle-derived mica megacryst from Cenozoic basanite from NUshan, Anhui Province has been determined by ion micro probe. The results demonstrate that δD and water content of the megacryst were heterogeneous on the micro scale, which resulted from reaction with meteoric water after being brought to the surface. The primary δD of mica megacrysts was about-23‰, suggesting the recycled crustal materials in its source. By combining these values with those of other researchers, it is believed that the hydrogen isotope composition of the mantle is heterogeneous at least on the large scale.

  11. Sulfur isotopic composition of modern seafloor hydrothermal sediment and its geological significance

    Institute of Scientific and Technical Information of China (English)

    曾志刚; 李军; 蒋富清; 秦蕴珊; 翟世奎


    A total of 1 264 sulfur isotopic values for modem seafloor hydrothermel sediments from different hydrothermal fidds have been collected. On this basis, combining our sulfur isotpic data for surface hydrothermal sediments from the Jade hydrohtermal field in the Okinawa Trough and the TAG hydrothermal field in the Mid-Atlantic Ridge, respectively, and comparing the sulfur isotopic compositions and analyzing their sources of sulfur in seafloor hydrothermal sediments from different geologic-tectonic setting, the results show that: ( 1 ) sulfur isotopic values of sulfides and sulfates in modern seafloor hydrothermal sediments are concentrated in a narrow range, δ34S values of sulfides vary from l × 10-3 to 9 × 10- 3, with a mean of 4.5 × 10- 3 ( n = 1 042), δ34S values of sulfates vary from 19 × 10- 3 to 24× 10-3, with a mean of 21.3× 10-3 (n =217); (2) comparing the sulfur isotopic compositions of hydrothermal sediments from the sediment-hosted hydrothermal fields, the range of sulfur isotopic values for hydrothermal sediments from the sediment-free hydrothermal fields is narrow relatively; (3) the differences of sulfur isotopic compositions in sulfides from different hydrothermal fields show the differences in the sources of sulfur. The sulfur of hydrothermal sulfides in the sediment-free mid-ocean ridges is mainly from mid-ocean ridge basalt, and partially from the reduced seawater sulfate, and it is the result of partially reduced seawater sulfate mixed with basaltic sulfur. In the sediment-hosted nid-ocean ridges and the back-arc basins, the volcanics, the sediments and the organic matters also can offer their sulfur for forming hydrothermal sulfides; (4) the variations of sulfur isotopic compositions and the different sources of sulfur for hydrothermal sediments may be attributed to the various physical-chemical characteristics of hydrothermal fluids, the magmatic evolution and the different geologic-tectonic settings of seafloor hydrothermal systems.

  12. Plutonium isotopes in the atmosphere of Central Europe: Isotopic composition and time evolution vs. circulation factors. (United States)

    Kierepko, Renata; Mietelski, Jerzy W; Ustrnul, Zbigniew; Anczkiewicz, Robert; Wershofen, Herbert; Holgye, Zoltan; Kapała, Jacek; Isajenko, Krzysztof


    This paper reports evidence of Pu isotopes in the lower part of the troposphere of Central Europe. The data were obtained based on atmospheric aerosol fraction samples collected from four places in three countries (participating in the informal European network known as the Ring of Five (Ro5)) forming a cell with a surface area of about 200,000km(2). We compared our original data sets from Krakow (Poland, 1990-2007) and Bialystok (Poland, 1991-2007) with the results from two other locations, Prague (Czech Republic; 1997-2004) and Braunschweig (Germany; 1990-2003) to find time evolution of the Pu isotopes. The levels of the activity concentration for (238)Pu and for ((239+240))Pu were estimated to be a few and some tens of nBqm(-3), respectively. However, we also noted some results were much higher (even about 70 times higher) than the average concentration of (238)Pu in the atmosphere. The achieved complex data sets were used to test a new approach to the problem of solving mixing isotopic traces from various sources (here up to three) in one sample. Results of our model, supported by mesoscale atmospheric circulation parameters, suggest that Pu from nuclear weapon accidents or tests and nuclear burnt-up fuel are present in the air.

  13. Middle Neoproterozoic (ca. 705-716 Ma) arc to rift transitional magmatism in the northern margin of the Yangtze Block: Constraints from geochemistry, zircon U-Pb geochronology and Hf isotopes (United States)

    Wang, Ruirui; Xu, Zhiqin; Santosh, M.; Xu, Xianbing; Deng, Qi; Fu, Xuehai


    The South Qinling Belt in Central China is an important window to investigate the Neoproterozoic tectono-magmatic processes along the northern margin of the Yangtze Block. Here we present whole-rock geochemistry, zircon U-Pb geochronology and Lu-Hf isotopes of a suite of Middle Neoproterozoic intrusion from the Wudang Uplift in South Qinling. Zircon LA-ICP-MS U-Pb ages reveal that these rocks were formed at ca. 705-716 Ma. Geochemical features indicate that the felsic magmatic rocks are I-type granitoids, belong to calcic- to calc-alkaline series, and display marked negative Nb, Ta and Ti anomalies. Moreover, the enrichment of light rare earth elements (LREEs) and large ion lithophile elements (LILEs), combined with depletion of heavy rare earth elements (HREEs) support that these rocks have affinity to typical arc magmatic rocks formed in Andean-type active continental margins. The REE patterns are highly to moderately fractionated, with (La/Yb)N = 5.13-8.10 in meta-granites, and 2.32-2.35 in granodiorite. The granitoids have a wide range of zircon εHf(t) values (-29.91 to 14.76) and zircon Hf two-stage model ages (696-3482 Ma). We suggest that the ca. 705-716 Ma granitoids were sourced from different degrees of magma mixing between partial melting of the overlying mantle wedge triggered by hydrous fluids released from subducted materials and crustal melting. The hybrid magmas were emplaced in the shallow crust accompanied by assimilation and fractional crystallization (AFC). Both isotopic and geochemical data suggest that the ca. 705-716 Ma felsic magmatic rocks were formed along a continental arc. These rocks as well as the contemporary A-type granite may mark a transitional tectonic regime from continental arc to rifting, probably related to slab rollback during the oceanic subduction beneath the northern margin of Yangtze Block.

  14. The effect of phosphomonoesterases on the oxygen isotope composition of phosphate (United States)

    von Sperber, Christian; Kries, Hajo; Tamburini, Federica; Bernasconi, Stefano M.; Frossard, Emmanuel


    Plants and microorganisms under phosphorus (P) stress release extracellular phosphatases as a strategy to acquire inorganic phosphate (Pi). These enzymes catalyze the hydrolysis of phosphoesters leading to a release of Pi. During the enzymatic hydrolysis an isotopic fractionation (ε) occurs leaving an imprint on the oxygen isotope composition of the released Pi which might be used to trace phosphorus in the environment. Therefore, enzymatic assays with acid phosphatases from wheat germ and potato tuber and alkaline phosphatase from Escherichia coli were prepared in order to determine the oxygen isotope fractionation caused by these enzymes. Adenosine 5‧ monophosphate and glycerol phosphate were used as substrates. The oxygen isotope fractionation caused by acid phosphatases is 20-30‰ smaller than for alkaline phosphatases, resulting in a difference of 5-7.5‰ in δ18O of Pi depending on the enzyme. We attribute the enzyme dependence of the isotopic fractionation to distinct reaction mechanisms of the two types of phosphatases. The observed difference is large enough to distinguish between the two enzymatic processes in environmental samples. These findings show that the oxygen isotope composition of Pi can be used to trace different enzymatic processes, offering an analytical tool that might contribute to a better understanding of the P-cycle in the environment.

  15. Carbon isotope composition of latex does not reflect temporal variations of photosynthetic carbon isotope discrimination in rubber trees (Hevea brasiliensis). (United States)

    Kanpanon, Nicha; Kasemsap, Poonpipope; Thaler, Philippe; Kositsup, Boonthida; Gay, Frédéric; Lacote, Régis; Epron, Daniel


    Latex, the cytoplasm of laticiferous cells localized in the inner bark of rubber trees (Hevea brasiliensis Müll. Arg.), is collected by tapping the bark. Following tapping, latex flows out of the trunk and is regenerated, whereas in untapped trees, there is no natural exudation. It is still unknown whether the carbohydrates used for latex regeneration in tapped trees is coming from recent photosynthates or from stored carbohydrates, and in the former case, it is expected that latex carbon isotope composition of tapped trees will vary seasonally, whereas latex isotope composition of untapped trees will be more stable. Temporal variations of carbon isotope composition of trunk latex (δ(13)C-L), leaf soluble compounds (δ(13)C-S) and bulk leaf material (δ(13)C-B) collected from tapped and untapped 20-year-old trees were compared. A marked difference in δ(13)C-L was observed between tapped and untapped trees whatever the season. Trunk latex from tapped trees was more depleted (1.6‰ on average) with more variable δ(13)C values than those of untapped trees. δ(13)C-L was higher and more stable across seasons than δ(13)C-S and δ(13)C-B, with a maximum seasonal difference of 0.7‰ for tapped trees and 0.3‰ for untapped trees. δ(13)C-B was lower in tapped than in untapped trees, increasing from August (middle of the rainy season) to April (end of the dry season). Differences in δ(13)C-L and δ(13)C-B between tapped and untapped trees indicated that tapping affects the metabolism of both laticiferous cells and leaves. The lack of correlation between δ(13)C-L and δ(13)C-S suggests that recent photosynthates are mixed in the large pool of stored carbohydrates that are involved in latex regeneration after tapping.

  16. Coupled isotopes of plant wax and hemicellulose markers record information on relative humidity and isotopic composition of precipitation

    Directory of Open Access Journals (Sweden)

    M. Tuthorn


    Full Text Available The δ2H isotopic composition of leaf waxes is used increasingly for paleohydrological and -climate reconstructions. However, it is challenging to disentangle past changes in the isotopic composition of precipitation and changes in evapotranspirative enrichment of leaf water. We analyzed δ2H on n-alkanes and fatty acids in topsoils along a climate transect in Argentina, for which we had previously measured δ18O on plant-derived sugars. Our results indicate that leaf wax biomarker δ2H values (δ2Hlipids primarily reflect δ2Hsource water (precipitation, but are modulated by evapotranspirative enrichment. A mechanistic model is able to produce the main trends in δ2Hlipids along the transect, but seems to slightly underestimate evapotranspirative enrichment in arid regions and overestimate it in grass-dominated ecosystems. Furthermore, the (i coupling of the δ2Hlipid and δ18Osugar biomarker results and (ii application of biosynthetic fractionation factors allows calculating the δ2H-δ18O isotopic composition of leaf water along the transect. This also yields the deuterium excess (d excess of leaf water, which mainly reflects evapotranspirative enrichment, and can be used to model relative air humidity (RH. The high correlation of modeled (reconstructed based on biomarker results and measured RH, as well as the good agreement between modeled and actual δ2H and δ18O of precipitation along the transect lends support to the coupled δ2Hlipid and δ18Osugar biomarker approach for future paleoclimate research.

  17. Molybdenum Isotopic Composition of the Archean Mantle As Inferred from Studies of Komatiites (United States)

    Greber, N. D.; Puchtel, I. S.; Nagler, T. F.; Mezger, K.


    Molybdenum isotopic composition has been shown to be a powerful tool in studies of planetary processes, e.g. estimating core formation temperatures [1,2]. However, Mo isotope compositions of terrestrial reservoirs are not well constrained. In order to better constrain the Mo isotopic composition of the early Earth's mantle, komatiites from four locations were analyzed for their Mo concentrations and isotopic compositions. Komatiites are particularly appropriate for this type of study because they formed by high degrees of partial melting of the mantle leading to a complete base metal sulfide removal from the residual mantle and the production of sulfur-undersaturated melts and thus a quantitative removal of Mo from the source into the melt. All samples, except for two strongly altered specimens specifically chosen to study the effects of secondary alteration, are very fresh having preserved most of their primary mineralogy. The Mo concentrations in komatiites range from 10 to 120 ng/g. Fresh komatiites have lighter δ98Mo (NIST SRM 3134 = 0.25‰, [3]) than altered samples. The estimated primary Mo isotope compositions of the studied komatiite melts range from 0.02 ± 0.16‰ to 0.19 ± 0.14‰ and are therefore indistinguishable within analytical uncertainty (2SD) from published values for chondritic meteorites (0.09 ± 0.04 ‰; 2SD; [2]) and lighter than the proposed average for Earth's continental crust (0.3 to 0.4‰ [4]). All data combined, although overlapping in errors, show a consistent trend of lighter δ98Mo and lower Mo concentrations in more melt-depleted mantle sources, indicating incompatible behaviour of Mo and preferential mobilization of heavy Mo isotopes during mantle melting. [1] Hin et al. (2013) EPSL, 379 [2] Burkhardt et al. (2014) EPSL, 391 [3] Nägler, et al. (2014) GGR, 38. [4] Voegelin et al. (2014) Lithos, 190-191.

  18. SHRIMP U-Pb dating and Hf isotopic analyses of Middle Ordovician meta-cumulate gabbro in central Qiangtang, northern Tibetan Plateau

    Institute of Scientific and Technical Information of China (English)


    Metabasites consisting of metamorphic ultra-mafic rocks, cumulate gabbro, gabbro (diabase), basalt, and plagiogranite are exposed at the Taoxinghu area in central Qiangtang, northern Tibetan Plateau. Zircon SHRIMP U-Pb dating for the cumulate gabbro yields a weighted mean age of 467±4 Ma, which is the oldest and most reliable magmatic age in this area. Zircon 176Hf/177Hf ratios range from 0.282615 to 0.282657, with εHf(t) values of 5.02±0.28, indicating that the cumulate gabbro was mainly derived from the depleted mantle. In addition, geochemical data of metabasites suggest that they have similar characteristics to those in the mid-ocean ridge basalts (MORB). The Taoxinghu metabasites may represent the fragment of Early Paleozoic ophiolite in the "Central Uplift" of the Qiangtang, northern Tibetan Plateau.

  19. Lead isotope studies of the Guerrero composite terrane, west-central Mexico: implications for ore genesis (United States)

    Potra, Adriana; Macfarlane, Andrew W.


    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

  20. Unexpected variations in the triple oxygen isotope composition of stratospheric carbon dioxide. (United States)

    Wiegel, Aaron A; Cole, Amanda S; Hoag, Katherine J; Atlas, Elliot L; Schauffler, Sue M; Boering, Kristie A


    We report observations of stratospheric CO2 that reveal surprisingly large anomalous enrichments in (17)O that vary systematically with latitude, altitude, and season. The triple isotope slopes reached 1.95 ± 0.05(1σ) in the middle stratosphere and 2.22 ± 0.07 in the Arctic vortex versus 1.71 ± 0.03 from previous observations and a remarkable factor of 4 larger than the mass-dependent value of 0.52. Kinetics modeling of laboratory measurements of photochemical ozone-CO2 isotope exchange demonstrates that non-mass-dependent isotope effects in ozone formation alone quantitatively account for the (17)O anomaly in CO2 in the laboratory, resolving long-standing discrepancies between models and laboratory measurements. Model sensitivities to hypothetical mass-dependent isotope effects in reactions involving O3, O((1)D), or CO2 and to an empirically derived temperature dependence of the anomalous kinetic isotope effects in ozone formation then provide a conceptual framework for understanding the differences in the isotopic composition and the triple isotope slopes between the laboratory and the stratosphere and between different regions of the stratosphere. This understanding in turn provides a firmer foundation for the diverse biogeochemical and paleoclimate applications of (17)O anomalies in tropospheric CO2, O2, mineral sulfates, and fossil bones and teeth, which all derive from stratospheric CO2.

  1. Isotopic composition of Murchison organic compounds: Intramolecular carbon isotope fractionation of acetic acid. Simulation studies of cosmochemical organic syntheses (United States)

    Yuen, G. U.; Cronin, J. R.; Blair, N. E.; Desmarais, D. J.; Chang, S.


    Recently, in our laboratories, samples of Murchison acetic acid were decarboxylated successfully and the carbon isotopic composition was measured for the methane released by this procedure. These analyses showed significant differences in C-13/C-12 ratios for the methyl and carboxyl carbons of the acetic acid molecule, strongly suggesting that more than one carbon source may be involved in the synthesis of the Murchison organic compounds. On the basis of this finding, laboratory model systems simulating cosmochemical synthesis are being studied, especially those processes capable of involving two or more starting carbon sources.

  2. Paleoproterozoic magmatism across the Archean-Proterozoic boundary in central Fennoscandia: Geochronology, geochemistry and isotopic data (Sm-Nd, Lu-Hf, O) (United States)

    Lahtinen, Raimo; Huhma, Hannu; Lahaye, Yann; Lode, Stefanie; Heinonen, Suvi; Sayab, Mohammad; Whitehouse, Martin J.


    The central Fennoscandia is characterized by the Archean-Proterozoic (AP) boundary and the Central Finland Granitoid Complex (CFGC), a roundish area of approximately 40,000 km2 surrounded by supracrustal belts. Deep seismic reflection profile FIRE 3A runs across these units, and we have re-interpreted the profile and crustal evolution along the profile using 1.92-1.85 Ga plutonic rocks as lithospheric probes. The surface part of the profile has been divided into five subareas: Archean continent (AC) in the east, AP, CFGC, boundary zone (BZ) and the Bothnian Belt (BB) in the west. There are 12 key samples from which zircons were studied for inclusions and analyzed (core-rim) by ion probe for U-Pb dating and oxygen isotopes, followed by analyzes for Lu-Hf by LA-MC-ICP-MS. The AC plutonic rocks (1.87-1.85 Ga) form a bimodal suite, where the proposed mantle source for the mafic rocks is 2.1-2.0 Ga metasomatized lower part of the Archean subcontinental lithospheric mantle (SCLM) and the source for the felsic melts is related plume-derived underplated mafic material in the lower crust. Variable degrees of contamination of the Archean lower crust have produced "subduction-like" Nb-Ta anomalies in spidergrams and negative εNd (T) values in the mafic-intermediate rocks. The felsic AC granitoids originate from a low degree melting of eclogitic or garnet-bearing amphibolites with titanite ± rutile partly prevailing in the residue (Nb-Ta fractionation) followed by variable degree of assimilation/melting of the Archean lower crust. The AP plutonic rocks (ca. 1.88 Ga) can be divided into I-type and A-type granitoids (AP/A), where the latter follow the sediment assimilation trend in ASI diagram, have high δ18O values (up to 8‰) in zircons and exhibit negative Ba anomalies (Rb-Ba-Th in spidergram), as found in sedimentary rocks. A mixing/assimilation of enriched mantle-derived melts with melts from already migmatized sedimentary rocks ± amphibolites is proposed. The CFGC is

  3. In situ observations of the isotopic composition of methane at the Cabauw tall tower site (United States)

    Röckmann, Thomas; Eyer, Simon; van der Veen, Carina; Popa, Maria E.; Tuzson, Béla; Monteil, Guillaume; Houweling, Sander; Harris, Eliza; Brunner, Dominik; Fischer, Hubertus; Zazzeri, Giulia; Lowry, David; Nisbet, Euan G.; Brand, Willi A.; Necki, Jaroslav M.; Emmenegger, Lukas; Mohn, Joachim


    High-precision analyses of the isotopic composition of methane in ambient air can potentially be used to discriminate between different source categories. Due to the complexity of isotope ratio measurements, such analyses have generally been performed in the laboratory on air samples collected in the field. This poses a limitation on the temporal resolution at which the isotopic composition can be monitored with reasonable logistical effort. Here we present the performance of a dual isotope ratio mass spectrometric system (IRMS) and a quantum cascade laser absorption spectroscopy (QCLAS)-based technique for in situ analysis of the isotopic composition of methane under field conditions. Both systems were deployed at the Cabauw Experimental Site for Atmospheric Research (CESAR) in the Netherlands and performed in situ, high-frequency (approx. hourly) measurements for a period of more than 5 months. The IRMS and QCLAS instruments were in excellent agreement with a slight systematic offset of (+0.25 ± 0.04) ‰ for δ13C and (-4.3 ± 0.4) ‰ for δD. This was corrected for, yielding a combined dataset with more than 2500 measurements of both δ13C and δD. The high-precision and high-temporal-resolution dataset not only reveals the overwhelming contribution of isotopically depleted agricultural CH4 emissions from ruminants at the Cabauw site but also allows the identification of specific events with elevated contributions from more enriched sources such as natural gas and landfills. The final dataset was compared to model calculations using the global model TM5 and the mesoscale model FLEXPART-COSMO. The results of both models agree better with the measurements when the TNO-MACC emission inventory is used in the models than when the EDGAR inventory is used. This suggests that high-resolution isotope measurements have the potential to further constrain the methane budget when they are performed at multiple sites that are representative for the entire European domain.

  4. Multiple sulfur isotope composition of oxidized Samoan melts and the implications of a sulfur isotope 'mantle array' in chemical geodynamics (United States)

    Labidi, J.; Cartigny, P.; Jackson, M. G.


    To better address how subducted protoliths drive the Earth's mantle sulfur isotope heterogeneity, we report new data for sulfur (S) and copper (Cu) abundances, S speciation and multiple S isotopic compositions (32S, 33S, 34S, 36S) in 15 fresh submarine basaltic glasses from the Samoan archipelago, which defines the enriched-mantle-2 (EM2) endmember. Bulk S abundances vary between 835 and 2279 ppm. About 17 ± 11% of sulfur is oxidized (S6+) but displays no consistent trend with bulk S abundance or any other geochemical tracer. The S isotope composition of both dissolved sulfide and sulfate yield homogeneous Δ33S and Δ36S values, within error of Canyon Diablo Troilite (CDT). In contrast, δ34S values are variable, ranging between +0.11 and +2.79‰ (±0.12‰ 1σ) for reduced sulfur, whereas oxidized sulfur values vary between +4.19 and +9.71‰ (±0.80‰, 1σ). Importantly, δ34S of the reduced S pool correlates with the 87Sr/86Sr ratios of the glasses, in a manner similar to that previously reported for South-Atlantic MORB, extending the trend to δ34S values up to + 2.79 ± 0.04 ‰, the highest value reported for undegassed oceanic basalts. As for EM-1 basalts from the South Atlantic ridge, the linear δ34S-87Sr/86Sr trend requires the EM-2 endmember to be relatively S-rich, and only sediments can account for these isotopic characteristics. While many authors argue that both the EM-1 and EM-2 mantle components record subduction of various protoliths (e.g. upper or lower continental crust, lithospheric mantle versus intra-metasomatized mantle, or others), it is proposed here that they primarily reflect sediment recycling. Their distinct Pb isotope variation can be accounted for by varying the proportion of S-poor recycled oceanic crust in the source of mantle plumes.

  5. Isotopic composition analysis and age dating of uranium samples by high resolution gamma ray spectrometry (United States)

    Apostol, A. I.; Pantelica, A.; Sima, O.; Fugaru, V.


    Non-destructive methods were applied to determine the isotopic composition and the time elapsed since last chemical purification of nine uranium samples. The applied methods are based on measuring gamma and X radiations of uranium samples by high resolution low energy gamma spectrometric system with planar high purity germanium detector and low background gamma spectrometric system with coaxial high purity germanium detector. The "Multigroup γ-ray Analysis Method for Uranium" (MGAU) code was used for the precise determination of samples' isotopic composition. The age of the samples was determined from the isotopic ratio 214Bi/234U. This ratio was calculated from the analyzed spectra of each uranium sample, using relative detection efficiency. Special attention is paid to the coincidence summing corrections that have to be taken into account when performing this type of analysis. In addition, an alternative approach for the age determination using full energy peak efficiencies obtained by Monte Carlo simulations with the GESPECOR code is described.

  6. Isotopic Composition of Xenon in Petroleum from the Shell Bullwinkle Field

    Indian Academy of Sciences (India)

    J Nuzzo*; M Hyman; M W Rowe; Mnraoz; R L Palma; J Westrich


    We have measured the abundance and isotopic composition of xenon in petroleum samples from the Shell Bullwinkle Field off the coast of Louisiana. We used an oxidation and purification procedure designed to insure complete extraction and clean up of xenon from the petroleum. The xenon isotopic composition was found to be similar to the atmospheric value for one petroleum sample. While the results of the second sample suggest possible enrichment of the heavier isotopes, the errors associated with these excesses preclude a definitive statement to that effect. No monoisotopic enrichment in 129Xe was detected in either sample, the presence of which might have allowed us to deduce the petroleum age. Our results represent only the second xenon measurement from petroleum, and the concentrations are within the range of values published in the earlier report.

  7. Isotope composition and volume of Earth´s early oceans

    DEFF Research Database (Denmark)

    Pope, Emily Catherine; Bird, Dennis K.; Rosing, Minik Thorleif


    Oxygen and hydrogen isotope compositions of Earth´s seawater are controlled by volatile fluxes among mantle, lithospheric (oceanic and continental crust), and atmospheric reservoirs. Throughout geologic time the oxygen mass budget was likely conserved within these Earth system reservoirs......, but hydrogen´s was not, as it can escape to space. Isotopic properties of serpentine from the approximately 3.8 Ga Isua Supracrustal Belt in West Greenland are used to characterize hydrogen and oxygen isotope compositions of ancient seawater. Archaean oceans were depleted in deuterium [expressed as Î...... in Earth´s oceans. Our calculations predict that the oceans of early Earth were up to 26% more voluminous, and atmospheric CH4 and CO2 concentrations determined from limits on hydrogen escape to space are consistent with clement conditions on Archaean Earth....

  8. Abnormal composition of carbon isotopes in underground alkaline waters of Kuzbass (United States)

    Shvartsev, S. L.; Lepokurova, O. E.; Ponomarchuk, V. A.; Domrocheva, E. V.; Sizikov, D. A.


    The first data on abnormally high δ13C values in hydrocarbonates (HCO 3 - ) dissolved in underground waters of coal deposits of Kuzbass (up to +30.9‰) are reported. It is shown that such an unusual isotope composition of waters results from the long, strictly directed interaction in the water-rock-gas-organic material system occurring under the conditions of hindered water exchange. Extensive fractionation of C isotopes is the result of the evolution of the water-rock-gas-coal system after penetration of infiltration waters into the coal deposits and their long interaction with all these components, rather than metamorphism of organic material upon its transformation into coal. With respect to such an approach, the isotope composition of dissolved C may indicate the duration of the evolution in the water-rock-gas-organic material system.

  9. HfO2/porous anodic alumina composite films for multifunctional data storage media materials under electric field control (United States)

    Qi, Li-Qian; Pan, Di-Ya; Li, Jun-Qing; Liu, Li-Hu; Sun, Hui-Yuan


    New materials for achieving direct electric field control of ferromagnetism and resistance behavior are highly desirable in the development of multifunctional data storage devices. In this paper, HfO2 nanoporous films have been fabricated on porous anodic alumina (PAA) substrates by DC-reactive magnetron sputtering. Electrically induced resistive switching (RS) and modulated room temperature ferromagnetism are simultaneously found in a Ag/HfO2/PAA/Al (Ag/HP/Al) heterostructure. The switching mechanism between low resistance state and high resistance state is generally attributed to the formation/rupture of conductive filaments which may consist of oxygen vacancies. The combination of the electric field control of magnetization change and RS makes HP films possible for the multifunctional data storage media materials.

  10. Isotopic composition of carbon and oxygen of carbonates of oil and gas-bearing deposits of Western Siberia

    Energy Technology Data Exchange (ETDEWEB)

    Golyshev, S.I.; Cherepnin, A.V.; Rozhnev, A.N.


    There is measured the isotopic composition of carbon and oxygen in 129 samples of carbonates and carbonate cements of oil and gas-bearing Paleozoic and Mezozoic deposits of Western Siberia. The isotopic composition of samples of marine deposits varies from -1.2 to +6.1% for carbon and from 19.8 to 29.1% for oxygen and has a mean isotopic composition of 1.9 to 24.8%. Catagenetic processes lead to lightening of the isotopic composition of secondary carbonate on the average by 5% for carbon and 9% for oxygen. The most intense lightening of isotopic composition is observed in samples disposed near oil and gas deposits.

  11. Isotope variations of dissolved Zn in the Rio Grande watershed, USA: The role of adsorption on Zn isotope composition (United States)

    Szynkiewicz, Anna; Borrok, David M.


    In order to better understand the factors influencing zinc (Zn) isotope composition in hydrological systems, we analyzed the δ66Zn of dissolved Zn in the streams and groundwater of the Upper and Middle Rio Grande watershed in Colorado and New Mexico, United States. The stream water samples have a wider variation of δ66Zn (-0.57 to + 0.41 ‰ relative to the JMC 3-0749-Lyon standard) than groundwater samples (-0.13 to + 0.12 ‰) and than samples from streams that are in close proximity to abandoned mining sites (+0.24 to + 0.40 ‰). Regional changes of bedrock geology, from primarily igneous rocks to primarily sedimentary rocks, have no resolvable effect on the δ66Zn of aqueous samples. Instead, an increase in water pH from 7.5 to 8.5 corresponds to a considerable decrease in the δ66Zn of dissolved Zn (R2 = - 0.37, p = 0.003, n = 22). Consequently, we link the observed Zn isotope variations to the process of adsorption of Zn onto suspended sediment and bedrock minerals (average Δ66Znadsorbed-dissolved = + 0.31 ‰). Our results are in good agreement with previous experimental and empirical studies suggesting that Zn adsorption leads to a residual dissolved pool enriched in light Zn isotopes. Given that anthropogenic Zn sources can also be responsible for lowering of δ66Zn, and may overlap with the pH/adsorption effect on δ66Zn, the latter needs to be carefully considered in future studies to differentiate between natural and anthropogenic factors influencing Zn isotopes in this and other aquatic systems.

  12. Calcium isotopic compositions as tracers of vegetation activity in boreal permafrost ecosystems (Kulingdakan watershed, Central Siberia) (United States)

    Bagard, M.; Schmitt, A.; Chabaux, F. J.; Viers, J.; Pokrovsky, O. S.; Prokushkin, A. S.; Stille, P.; Dupré, B.


    In this work, we propose to investigate the geochemical potential of calcium isotopic fractionations in a forested boreal watershed to trace the impact of vegetation activity. This is the first study carried out in a geographical area characterized by deep and continuous permafrost. For this survey, we measured Ca and Sr isotopic compositions in the different compartments (stream waters, soil solutions, precipitations, rock, soils and soil leachates, vegetation) of a 4,100 ha Siberian watershed, the Kulingdakan watershed (Putorana Plateau, Central Siberia). Our results show that the activity of the vegetation is the only process that fractionates significantly calcium isotopes within the watershed. Indeed, Ca uptake by plants and its subsequent storage in larch tree organs favours 40Ca relatively to 44Ca. Vegetation decomposition releases light δ44/40Ca that affects calcium isotopic compositions of soil solution and soil exchangeable fractions. However, this biological impact is significant only for the South-facing slope of the watershed. Indeed, soil pools from the North-facing slope present no imprint of organic matter degradation in their δ44/40Ca signatures. Furthermore, the major difference between South- and North- facing slopes lies in the importance of the vegetation and its decomposition rate. Thus, we propose that in boreal permafrost areas with limited runoff, the available stock of biomass is critical to induce or not a significant vegetation impact on the calcium isotopic compositions in the soil-water system. As a consequence, the study of preserved calcium isotopic compositions in paleosoil exchangeable phases might bring relevant information on the evolution of biological activity at the watershed scale.

  13. Stable water isotopic composition of the Antarctic subglacial Lake Vostok: implications for understanding the lake's hydrology. (United States)

    Ekaykin, Alexey A; Lipenkov, Vladimir Y; Kozachek, Anna V; Vladimirova, Diana O


    We estimated the stable isotopic composition of water from the subglacial Lake Vostok using two different sets of samples: (1) water frozen on the drill bit immediately after the first lake unsealing and (2) water frozen in the borehole after the unsealing and re-drilled one year later. The most reliable values of the water isotopic composition are: -59.0 ± 0.3 ‰ for oxygen-18, -455 ± 1 ‰ for deuterium and 17 ± 1 ‰ for d-excess. This result is also confirmed by the modelling of isotopic transformations in the water which froze in the borehole, and by a laboratory experiment simulating this process. A comparison of the newly obtained water isotopic composition with that of the lake ice (-56.2 ‰ for oxygen-18, -442.4 ‰ for deuterium and 7.2 ‰ for d-excess) leads to the conclusion that the lake ice is very likely formed in isotopic equilibrium with water. In turn, this means that ice is formed by a slow freezing without formation of frazil ice crystals and/or water pockets. This conclusion agrees well with the observed physical and chemical properties of the lake's accreted ice. However, our estimate of the water's isotopic composition is only valid for the upper water layer and may not be representative for the deeper layers of the lake, so further investigations are required.

  14. The carbon isotope composition of atmospheric CO 2 in Paris (United States)

    Widory, David; Javoy, Marc


    One characteristic of air pollution in the urban environment is high CO 2 concentrations resulting from human activities. Determining the relative contributions of the different CO 2 sources can be addressed simply and elegantly by combining isotope and concentration measurements. Using this approach on atmospheric CO 2 samples collected in Paris, its suburbs and the open country provides fairly accurate conclusions. Our results show that air pollution within the first few metres above ground results basically from binary mixtures among which road traffic is the main contributor and, in particular, vehicles using unleaded gasoline (˜90% of the total). Heating sources, which account for 50% of the CO 2 input below the atmospheric inversion level, and vehicles using diesel contribute very little. Human respiration has a recognisable signature at street level under certain circumstances. The combined isotope and concentration analysis provides a sensitive tracer of local variations, even detecting the occasional prevalence of human respiration and the onset of actions in which natural gas is burnt. It also detects surprising inlets of 'clean air' (CO 2-wise) in the very centre of the city.

  15. The isotopic composition of methane in polar ice cores (United States)

    Craig, H.; Chou, C. C.; Welhan, J. A.; Stevens, C. M.; Engelkemeir, A.


    Air bubbles in polar ice cores indicate that about 300 years ago the atmospheric mixing ratio of methane began to increase rapidly. Today the mixing ratio is about 1.7 parts per million by volume, and, having doubled once in the past several hundred years, it will double again in the next 60 years if current rates continue. Carbon isotope ratios in methane up to 350 years in age have been measured with as little as 25 kilograms of polar ice recovered in 4-meter-long ice-core segments. The data show that: (1) in situ microbiology or chemistry has not altered the ice-core methane concentrations, and (2) that the carbon-13 to carbon-12 ratio of atmospheric CH4 in ice from 100 years and 300 years ago was about 2 per mil lower than at present. Atmospheric methane has a rich spectrum of isotopic sources: the ice-core data indicate that anthropogenic burning of the earth's biomass is the principal cause of the recent C-13H4 enrichment, although other factors may also contribute.

  16. Diet control on carbon isotopic composition of land snail shell carbonate

    Institute of Scientific and Technical Information of China (English)

    LIU ZongXiu; GU ZhaoYan; WU NaiQin; XU Bing


    Carbon isotope compositions for both the carbonate shells and soft bodies (organic tissue) of living land snails collected mostly from the Loess Plateau, China have been measured. The result shows that δ13C values range from -13.1‰ to -4.3‰ for the aragonite shell samples and from -26.8‰ to -18.0‰ for the soft body samples. Although the shells are enriched in 13C relative to the bodies averagely by 14.2(±0.8)‰, the shell δ13Ca values are closely correlated to the body δ13Corg values, expressed as δ13Ca = 1.021 δ13Corg + 14.38 (R = 0.965; N = 31). This relationship indicates that δ13Ca is primarily a function of the isotopic composition of the snail diets since previous studies have proved that the snail body is the same as their food in carbon isotope composition. In other words, carbon isotope compo-sition of the carbonate shell can be used as a proxy to estimate the dietary 13C abundance of the land snails. The data also support that the 13C enrichment of the carbonate shells results mainly from the equilibrium fractionations between the metabolic CO2, HCO3- in the hemolymph and shell aragonite, and partially from kinetic fractionations when snail shells form during their activity.

  17. The atomic weight and isotopic composition of boron and their variation in nature

    Energy Technology Data Exchange (ETDEWEB)

    Holden, N.E.


    The boron isotopic composition and atomic weight value and their variation in nature are reviewed. Questions are raised about the previously recommended value and the uncertainty for the atomic weight. The problem of what constitutes an acceptable range for normal material and what should then be considered geologically exceptional is discussed. Recent measurements make some previous decisions in need of re-evaluation.

  18. Impact of metabolism and growth phase on the hydrogen isotopic composition of microbial fatty acids

    NARCIS (Netherlands)

    Heinzelmann, S.M.; Villanueva, L.; Sinke-Schoen, D.; Sinninghe Damsté, J.S.; Schouten, S.; Van der Meer, M.T.J.


    Microorganisms are involved in all elemental cycles and therefore it is important to study their metabolism in the natural environment. A recent technique to investigate this is the hydrogen isotopic composition of microbial fatty acids, i.e., heterotrophic microorganisms produce fatty acids enriche

  19. Interpretation of groundwater origin in the Velenje coal mine on the basis of isotope composition

    Directory of Open Access Journals (Sweden)

    Janko Urbanc


    Full Text Available The aim of the investigation was to determine the isotopic properties of cave waters from the Velenje coal mine and define the recharge areas of individual aquifers. With regard to the oxygen isotope composition, groundwater in the Velenje coal mine can beclassified into three types. Typical d18O values of the first type are around -9 ‰ and are found in surface waters in the vicinity of the mine, therefore it is supposed that these waters are recharged locally. The second type is represented mainly by waters from thelower part of the pliocene aquifer. The average oxygen composition of these waters is about -11 ‰. This isotope composition is considerably different from the isotope composition of recent waters from the mine’s vicinity, which leads to the conclusion that these are older, fossile waters. These waters also have a very high degree of mineralization and consequently conductivity. Waters of the third type have average δ18O values around -10 ‰ and originate mainly from triassic dolomites. These waters could be a mixture of recentand old waters, but it is also possible that they flow into the coal mine from the higher areas of Paški Kozjak.

  20. Soil moisture effects on the carbon isotope composition of soil respiration (United States)

    Claire L. Phillips; Nick Nickerson; David Risk; Zachary E. Kayler; Chris Andersen; Alan Mix; Barbara J. Bond


    The carbon isotopic composition (δ13C) of recently assimilated plant carbon is known to depend on water-stress, caused either by low soil moisture or by low atmospheric humidity. Air humidity has also been shown to correlate with the δ13C of soil respiration, which suggests indirectly that recently fixed photosynthates...

  1. Single-molecule fluorescence autocorrelation experiments on pentacene : The dependence of intersystem crossing on isotopic composition

    NARCIS (Netherlands)

    Brouwer, A.C.J.; Köhler, J.; Oijen, A.M. van; Groenen, E.J.J.; Schmidt, J.


    Single pentacene molecules containing 13C or 1H in a pentacene-d14 doped p-terphenyl crystal have been studied by fluorescence autocorrelation. The triplet dynamics has been analyzed and a systematic dependence of the S1→T1 intersystem crossing rate on isotopic composition was found. This variation

  2. New approach to global barium cycle understanding: barium isotopic composition of marine carbonates and seawater. (United States)

    Pretet, Chloé; Nägler, Thomas F.; Reynaud, Stéphanie; de Lange, Gert J.; Turpin, Mélanie; Immenhauser, Adrian; Böttcher, Michael E.; Samankassou, Elias


    In this communication we present the Ba isotope fractionation (delta137/134Ba) study on marine carbonates and seawater, initiated to gain a first order view of the marine Ba isotope cycle. A special focus is the question whether the nutrient type distribution of Ba in the water column, as well as different Ba sources, are reflected in Ba isotope ratios of carbonate archives. The approach ultimately aims to provide an improved Ba based paleonutrient proxy. The data set is composed of carbonates (micrites and limestone standard), coral skeleton and seawater (IAPSO standard and Mediterranean seawater). Part of the corals were cultured in monitored environments (CSM, Monaco) others originate from natural environments (shallow and warm water corals from the Bahamas/Florida and cold water corals from the Norwegian shelf). The analytical procedure includes the application of a 130Ba/135Ba double spike, a cation exchange column followed by isotope measurements on a Nu Instruments Multicollector ICP-MS. The Ba fractionation of the samples is compared to a Ba nitrate standard solution and a standard natural limestone BSC-CRM 393 (0.05 ± 0.04 ‰, 2SEM). No isotopic fractionation has been observed in the limestone standard and micrites (N=8) (-0.01 ± 0.04 ‰, 2SEM) compared to the Ba nitrate standard. On the contrary, coral skeletons show a significant positive fractionation (mean = 0.4 ± 0.05 ‰, 2 SEM). No significant difference was found between different cultured coral species. Thus no species-specific fractionation is identified within the same environmental conditions. Diagenetic influence on Ba isotopic composition was further tested on 5 natural samples with varying calcite to aragonite ratios (0 to 0.3). No significant effect was observed. Moreover, the Ba isotope composition seems independant from the Ba concentration in the studied coral skeleton, within our measurement resolution. Seawater isotopic composition (-0.05 ± 0.07 ‰, 2SD) is lighter than coral

  3. The Cl Isotope Composition of the Moon as evidence for an Anhydrous Mantle (Invited) (United States)

    Sharp, Z. D.; Shearer, C., Jr.; McKeegan, K. D.; Barnes, J.; Wang, Y.


    The chlorine isotope composition of primitive terrestrial basalts and carbonaceous chondrites cover a narrow range centered around 0‰ with a total variation of ± 0.5‰. In contrast, the chlorine isotope composition of bulk samples and in situ ion microprobe analyses of lunar basalts and glasses cover a range of 25‰. Three possibilities were considered to explain the large spread: 1) initial isotopic heterogeneities, 2) devolatilization from solar wind/micrometeorite bombardment, 3) degassing under anhydrous conditions. The first of these possibilities is rejected because the Moon went through an magma ocean stage which would have homogenized any isotopic heterogeneities. To examine surface effects, we chose samples that have extremely different degrees of surface exposure. We find no correlation between the Cl isotope composition and surface exposure. We also conducted a laboratory experiment in which a thin film of NaCl was bombarded with a proton source for 24 hours with no change in Cl isotope composition. The third possibility is that the fractionation is explained by the anhydrous character of the Moon. On Earth, the volatiling Cl species is HCl. HCl is known to preferentially incorporate 37Cl relative to 35Cl due to the high bond strength of the molecule. This is offset by the higher translational velocity of H35Cl, so that overall, there is very little Cl isotope fractionation during degassing. We propose that lunar basalts were anhydrous and the volatile Cl species were metal chlorides, such as ZnCl2, NaCl, FeCl2, etc. The bond strength of metal chlorides and Cl dissolved in a basalt are similar, so that fractionation is caused mainly by volatilization, with the light isotopologue preferentially lost to the vapor phase. This idea is supported by the consistent lower Cl isotope ratios of water soluble salt fraction (~10 ‰ lower) and the lowest lunar Cl isotope values close to those of bulk Earth. The H content of lunar magmas must have been lower

  4. Isotopic composition and neutronics of the Okelobondo natural reactor (United States)

    Palenik, Christopher Samuel

    The Oklo-Okelobondo and Bangombe uranium deposits, in Gabon, Africa host Earth's only known natural nuclear fission reactors. These 2 billion year old reactors represent a unique opportunity to study used nuclear fuel over geologic periods of time. The reactors in these deposits have been studied as a means by which to constrain the source term of fission product concentrations produced during reactor operation. The source term depends on the neutronic parameters, which include reactor operation duration, neutron flux and the neutron energy spectrum. Reactor operation has been modeled using a point-source computer simulation (Oak Ridge Isotope Generation and Depletion, ORIGEN, code) for a light water reactor. Model results have been constrained using secondary ionization mass spectroscopy (SIMS) isotopic measurements of the fission products Nd and Te, as well as U in uraninite from samples collected in the Okelobondo reactor zone. Based upon the constraints on the operating conditions, the pre-reactor concentrations of Nd (150 ppm +/- 75 ppm) and Te (<1 ppm) in uraninite were estimated. Related to the burnup measured in Okelobondo samples (0.7 to 13.8 GWd/MTU), the final fission product inventories of Nd (90 to 1200 ppm) and Te (10 to 110 ppm) were calculated. By the same means, the ranges of all other fission products and actinides produced during reactor operation were calculated as a function of burnup. These results provide a source term against which the present elemental and decay abundances at the fission reactor can be compared. Furthermore, they provide new insights into the extent to which a "fossil" nuclear reactor can be characterized on the basis of its isotopic signatures. In addition, results from the study of two other natural systems related to the radionuclide and fission product transport are included. A detailed mineralogical characterization of the uranyl mineralogy at the Bangombe uranium deposit in Gabon, Africa was completed to improve

  5. Elemental and isotopic compositions of the hydrothermal sulfide on the East Pacific Rise near 13°N

    Institute of Scientific and Technical Information of China (English)


    The mineralogical,elemental,and isotopic characteristics of a hydrothermal sulfide sample from one dredge station (12°42.30’N,103°54.48’W,water depth 2655 m) on the East Pacific Rise near 13°N were analyzed.The hydrothermal sulfide was composed mainly of sphalerite,chalcopyrite,and pyrite and was a Zn-rich sulfide;in layer ep-s-1,goethite formed by secondary oxidation was found.The concentrations of rare elements,such as Li (0.15×10-6-0.30×10-6),Be (0.01×10-6-0.05×10-6),Zr (73.8×10-9-1344×10-9),Nb (8.14×10-9-64.7×10-9),Hf (2.54×10-9-28.0×10-9),and Ta (0.203×10-9-1.21×10-9),were far lower in the hydrothermal sulfide than in the ocean crust,whereas the content of Au was higher and the contents of Co,Ni,Sr,Cs,Ba,Bi,and U were low.The correlations between Zn and Cr,Cd and Ga,Cu and P,P and In (R2 > 0.8) were positive,whereas those between Zn and Fe,Cu,and Ba (R2 > 0.8) were distinctly negative.From low-temperature mineral assemblages to high-temperature mineral assemblages,the spatial distributions of dispersive and rare elements (e.g.In,Li,Cs) in the hydrothermal sulfide displayed corresponding variations.The variations observed in some elements (e.g.,Cd,Cs,P) are controlled by Zn,Fe,and Cu sulfides,respectively.Seafloor weathering accounts for the enrichment of V,Mn,and rare earth elements (REE) in the henna sulfide-oxidation layer that bears the secondary oxide mineral,leading to identical REE patterns for this layer (ep-s-1) and seawater.Seafloor weathering also distinctly affects the correlations between the element ratios of the hydrothermal sulfide.From high-temperature mineral assemblages to low-temperature mineral assemblages,Fe content and δ 34S value of the hydrothermal sulfide increase gradually,and Zn content and lead isotopic ratios decrease gradually on the contrary,which indicate the influences of seawater on elements and the sulfur and lead isotopic compositions enhance gradually during the formation of hydrothermal sulfides.

  6. Subduction-related Late Carboniferous to Early Permian Magmatism in the Eastern Pontides, the Camlik and Casurluk plutons: Insights from geochemistry, whole-rock Sr-Nd and in situ zircon Lu-Hf isotopes, and U-Pb geochronology (United States)

    Karsli, Orhan; Dokuz, Abdurrahman; Kandemir, Raif


    Late Carboniferous to early Permian granitoid rocks represent a volumetrically minor component of the Eastern Pontide lithosphere, but they preserve useful information about the region's tectonomagmatic history. The Casurluk and Camlik plutons primarily consist of gabbro, gabbroic diorite, diorite, monzogabbro, monzodiorite and monzonite, which intrude early to middle Carboniferous granitic basement rocks in the region. In this study, we use in situ zircon U-Pb ages and Lu-Hf isotopic values, whole-rock Sr-Nd isotopic values, and mineral chemistry and geochemistry of these plutons to determine petrogenesis and crustal evolution; we also discuss geodynamic implications. LA-ICP-MS zircon U-Pb dating of magmatic zircons from the rocks suggests that the plutons were emplaced during the late Carboniferous to early Permian (302 Ma). The metaluminous and I-type intrusive rocks belong to the high-K calc-alkaline series. In addition, they are relatively enriched in light rare earth elements (LREEs) and large-ion lithophile elements (LILEs); they are depleted in heavy rare earth elements (HREEs) and high field strength elements (HFSEs), such as Nb and Ti. All of the samples have homogeneous initial ISr values (0.70675 to 0.70792) and low εNd (t) values (- 5.1 to - 3.3). Zircons from the rocks of both plutons have uniform negative to slightly positive εHf (t) values (- 3.5 to 1.4) and old Hf two-stage model ages (1323 to 1548 Ma), implying that they have the same source, as well as suggesting the involvement of old enriched lithospheric mantle materials during their magma genesis. These results, combined with the εHf (t) values and two-stage model ages, demonstrate that the primary magmas were derived from partial melting of old lithospheric mantle material metasomatized by subduction-related fluids. Considering other regional geological data from the Sakarya Zone where these plutons formed, we conclude that late Carboniferous to early Permian magmatism in the area

  7. Oxygen and nitrogen isotopic composition of nitrate in commercial fertilizers, nitric acid, and reagent salts. (United States)

    Michalski, Greg; Kolanowski, Michelle; Riha, Krystin M


    Nitrate is a key component of synthetic fertilizers that can be beneficial to crop production in agro-ecosystems, but can also cause damage to natural ecosystems if it is exported in large amounts. Stable isotopes, both oxygen and nitrogen, have been used to trace the sources and fate of nitrate in various ecosystems. However, the oxygen isotope composition of synthetic and organic nitrates is poorly constrained. Here, we present a study on the N and O isotope composition of nitrate-based fertilizers. The δ(15)N values of synthetic and natural nitrates were 0 ± 2 ‰ similar to the air N2 from which they are derived. The δ(18)O values of synthetic nitrates were 23 ± 3 ‰, similar to air O2, and natural nitrate fertilizer δ(18)O values (55 ± 5 ‰) were similar to those observed in atmospheric nitrate. The Δ(17)O values of synthetic fertilizer nitrate were approximately zero following a mass-dependent isotope relationship, while natural nitrate fertilizers had Δ(17)O values of 18 ± 2 ‰ similar to nitrate produced photochemically in the atmosphere. These narrow ranges of values can be used to assess the amount of nitrate arising from fertilizers in mixed systems where more than one nitrate source exists (soil, rivers, and lakes) using simple isotope mixing models.

  8. Impacts of microbial community composition on isotope fractionation during reductive dechlorination of tetrachloroethylene. (United States)

    Dong, Yiran; Butler, Elizabeth C; Philp, R Paul; Krumholz, Lee R


    Isotope fractionation has been used with increasing frequency as a tool to quantify degradation of chlorinated aliphatic pollutants in the environment. The objective of this research was to determine if the electron donor present in enrichment cultures prepared from uncontaminated sediments influenced the extent of isotope fractionation of tetrachloroethylene (PCE), either directly, or through its influence on microbial community composition. Two PCE-degrading enrichment cultures were prepared from Duck Pond (DP) sediment and were incubated with formate (DPF) or H(2) (DPH) as electron donor. DPF and DPH were significantly different in both product distribution and extent of isotope fractionation. Chemical and isotope analyses indicated that electron donors did not directly affect the product distribution or the extent of isotope fractionation for PCE reductive dechlorination. Instead, restriction fragment length polymorphism (RFLP) and sequence analysis of the 16S rRNA clone libraries of DPF and DPH identified distinct microbial communities in each enrichment culture, suggesting that differences in microbial communities were responsible for distinct product distributions and isotope fractionation between the two cultures. A dominant species identified only in DPH was closely related to known dehalogenating species (Sulfurospirillum multivorans and Sulfurospirillum halorespirans) and may be responsible for PCE degradation in DPH. Our study suggests that different dechlorinators exist at the same site and can be preferentially stimulated by different electron donors, especially over the long-term (i.e., years), typical of in-situ ground water remediation.

  9. Zircon U-Pb age, Hf isotope and geochemistry of Carboniferous intrusions from the Langshan area, Inner Mongolia: Petrogenesis and tectonic implications (United States)

    Liu, Min; Zhang, Da; Xiong, Guangqiang; Zhao, Hongtao; Di, Yongjun; Wang, Zhong; Zhou, Zhiguang


    Late Paleozoic was a critical period for the tectonic evolution of the northern margin of the Alxa-North China craton, but the evolutionary history is not well constrained. The Carboniferous intrusions in the Langshan area in the western part of the northern margin of the Alxa-North China craton are mainly composed of tonalite, quartz diorite, olivine gabbro and pyroxene peridotite. Zircon LA-ICP-MS U-Pb dating indicates that the Langshan Carboniferous intrusions were emplaced at ca. 338-324 Ma. The quartz diorites are characterized by high amounts of compatible trace elements (Cr, Ni and V) and high Mg# values, which may suggest a significant mantle source. The positive Pb and negative Nb-Ta-Ti anomalies, the variable εHf(t) (-6.9 to 2.0) values and the old Hf model ages (1218-1783 Ma) imply some involvement of ancient continental materials in its petrogenesis. The tonalite has relatively high Sr/Y ratios, low Mg#, Yb and Y contents, features of adakite-like rocks, negative εHf(t) values (-9.8 to -0.1) and older Hf model ages (1344-1953 Ma), which suggest significant involvement of ancient crust materials and mantle-derived basaltic component in its petrogenesis. The high Mg# values, high Cr and Ni contents, and low Zr and Hf contents of the mafic-ultramafic rocks show evidence of a mantle source, and the relatively low zircon εHf(t) values (-5.9 to 3.2) might point to an enriched mantle. The trace element characteristics indicate the influence of subducted sediments and slab-derived fluids. In the tectonic discrimination diagrams, all the rocks plot in subduction-related environment, such as volcanic arc and continental arc. Considering the regional geology, we suggest that the Carboniferous intrusions in the Langshan area were likely emplaced during the late stage of the southward subduction of the Paleo-Asian Ocean plate, which formed a continental arc along the northern margin of the Alxa-North China craton.

  10. Sedimentary nitrate reduction and its effect on the N-isotopic composition of oceanic nitrate (United States)

    Lehmann, M. F.; Sigman, D. M.; McCorkle, D. C.


    A prerequisite for assessing denitrification fluxes in a specific environment using water column nitrate N isotope ratios is the knowledge of the expressed N isotope effects of water column and/or benthic denitrification in this environment. Here, we aim at assessing the effects of benthic nitrogen cycling on the N isotopic composition of the oceanic nitrate pool in deep-sea sediments, which are believed to harbour a large portion of the global benthic denitrification. We report 15N/14N ratios of pore water nitrate in pelagic sediments from the deep Bering Sea, where benthic nitrate reduction has previously been identified as a significant sink of fixed nitrogen. Porewater profiles from multicores indicate strong 15N enrichment in porewater nitrate at all stations, as one goes deeper in the sediments and nitrate concentrations decrease (δ15N generally reached 25-35‰). Our data are consistent with variable biological isotope effect (ɛ) for dissimilatory nitrate reduction ranging between 13 to 30 ‰. A one-dimensional diffusion-reaction model including organic matter degradation, nitrification, and denitrification indicates that, although denitrification leads to a pore water nitrate pool that is enriched in 15N, N isotope fractionation is poorly expressed at the scale of sediment-water nitrate exchange, independent of whether sediments are a net sink or a net source of nitrate. The apparent nitrate isotope effect of sedimentary denitrification on nitrate in overlying waters is generally below 2‰, as a result of diffusive transport limitation into, and within, the sediments and/or the production of light nitrate during nitrification. Thus, our data suggest that the low expressed isotope effect of benthic denitrification observed previously in reactive shelf sediments also applies to deep-sea sediments. However, where ammonium fluxes out of the sediments, it is enriched in 15-N, and may ultimately lead to an N-isotopic enrichment of the water-column nitrate

  11. Influence of sea ice cover on evaporation and water vapour isotopic composition in the Arctic (United States)

    Bonne, Jean-Louis; Werner, Martin; Meyer, Hanno; Kipfstuhl, Sepp; Rabe, Benjamin; Behrens, Melanie; Schönicke, Lutz; Steen-Larsen, Hans Christian


    Since July 2015, water stable isotopes (HDO and H218O) have been measured at two Arctic facilities: during the summer on board of the research vessel Polarstern, and year-round at the Siberian coastal site of Samoylov, situated in the Lena delta (N 72°22', E 126°29'), close to the Laptev Sea. In both places, the isotopic composition of water vapour is analysed continuously in surface air. Additional isotopic measurements are performed on a daily basis in ocean surface water samples taken on Polarstern and on an event basis from precipitation sampled in Samoylov. The two Polarstern summer campaigns cover a large region of the western Artic Ocean, including a one-month campaign in the central and eastern Arctic crossing the North Pole in September 2015, with very cold conditions (up to -20°C). Combining ocean and atmospheric observations from Polarstern allows an evaluation of local surface water evaporation and its isotopic fingerprint relative to the oceanic and meteorological conditions as well as the partial sea ice cover. In the central and eastern Arctic, a large area of complete sea ice cover also revealed a strong impact on the advected moisture above the ice cap under very cold conditions. A first year of Siberian observations at Samoylov depicted a large seasonal variability, with extremely dry and isotopically depleted winter values. Contrasted seasonal isotopic regimes might be utilized for identifying moisture sources changes in the region, such as ocean surface closure by sea ice, or freezing of the Lena River. Besides documenting the present meteorology and changes in the Arctic, our measurements will contribute to a better interpretation of regional paleoclimate records based on water isotopes and to the evaluation of climate models in the Arctic. A first model-data comparison of our measurements with simulation results by the isotope-enabled atmospheric general circulation model ECHAM5-wiso have revealed relevant model biases in the Arctic realm.

  12. Regulation of Isotopic Composition of Water - way of Improvement of Cosmonauts Drinking Water Functional Properties (United States)

    Kulikova, Ekaterina; Utina, Dina; Vorozhtsova, Svetlana; Severyuhin, Yuri; Abrosimova, Anna; Sinyak, Yuri; Ivanov, Alexander

    The problem in providing drinking water to cosmonauts is solved - at this moment there is a task to improve the functional properties of the water. One of the perspectives of this trend is the use of light isotopic water. The animal studies have shown that long-term consumption of water with a depletion of deuterium and oxygen heavy isotopes accelerates the rise of mass non-irradiated mice, the phase fluctuations reducing or increasing hematological parameters were having adaptive nature. These fluctuations didn’t overcome values beyond the physiological norm of this type of animal. It is established that the therapeutic use of light isotopic water with 35 - 90 ppm in deuterium increases the survival of irradiated mice by an average of 30%, contributes to the preservation of irradiated animals body weight. Treatment of acute radiation sickness with light isotopic water stimulates hematopoietic recovery. At the same time, keeping mice drinking light isotopic water for 7 - 8 days before the irradiation (from 4 to 8.5 Gr) has no effect on the level of radio resistance. Longer keeping mice on light isotopic water, for 14 -21 days - reduction in life expectancy, animal mass, bone marrow cellularity and the level of white blood cells in irradiated animals is noted. It was established that keeping mice on light isotopic water for 14 days before exposure in experimental animals causes an increase in the mitotic index and the frequency of formation of aberrant mitosis after 24 hours of Co(60) gamma radiation in doses of 1 , 2, and 4 Gr. Thus, it is clear that the regulation of the isotopic composition of drinking water - way to improve its functional properties.

  13. The influence of traffic and wood combustion on the stable isotopic composition of carbon monoxide

    Directory of Open Access Journals (Sweden)

    M. Saurer


    Full Text Available Carbon monoxide in the atmosphere is originating from various combustion and oxidation processes. Recently, the proportion of CO resulting from the combustion of wood for domestic heating may have increased due to political measures promoting this renewable energy source. Here, we used the stable isotope composition of CO (δ13C and δ18O for the characterization of different CO sources in Switzerland, along with other indicators for traffic and wood combustion (NOx-concentration, aerosol light absorption at different wavelengths. We assessed diurnal variations of the isotopic composition of CO at 3 sites during winter: a village site dominated by domestic heating, a site close to a motorway and a rural site. The isotope ratios of wood combustion emissions were studied at a test facility, indicating significantly lower δ18O of CO from wood combustion compared to traffic emissions. At the village and the motorway site, we observed very pronounced diurnal δ18O-variations of CO with an amplitude of up to 8‰. Solving the isotope mass balance equation for three distinct sources (wood combustion, traffic, clean background air resulted in diurnal patterns consistent with other indicators for wood burning and traffic. The average night-time contribution of wood-burning to total CO was 70% at the village site, 49% at the motorway site and 29% at the rural site based on the isotope mass balance. The results, however, depend strongly on the pure source isotope values, which are not very well known. We therefore additionally applied a combined CO/NOx-isotope model for verification. Here, we separated the CO emissions into different sources based on distinct CO/NOx emissions ratios for wood combustion and traffic, and inserted this information in the isotope mass balance equation. Accordingly, a highly significant agreement between measured and calculated δ18

  14. Isotopic Composition of Gaseous Elemental Mercury (Hg0) at Various Sites in Japan (United States)

    Yamakawa, A.; Moriya, K.; Yoshinaga, J.


    Mercury (Hg) is a toxic heavy metal, which exists in various chemical forms in the environmental system. In the atmosphere, Hg exists in three forms (Hg0(g), Hg+2(g), and Hg(p)). Hg0(g) is the dominant species of atmospheric Hg, accounting for >95% of the total Hg in the atmosphere. Because Hg0(g) is highly volatile and has limited solubility in water, it cannot be easily removed by wet or dry deposition processes. Therefore, the residence time of Hg0(g) in the atmosphere is relatively long (1 to 2 years), allowing long-range transport from mercury emission source(s). Conversely, Hg+2(g) and Hg(p) are effectively removed from the atmosphere through wet and dry depositions. The determination of mercury source attribution using quantitative data is challenging because Hg0(g) may be deposited on an area upon oxidation to Hg+2(g) and associated with aerosols and particulates to form Hg(p) while the global cycling of Hg0(g). Over the last decade, the development of analytical methods of highly precise Hg isotopic measurements demonstrated mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) of Hg isotopes in environmental samples. For instance, MDF of Hg isotopes is thought to occur during various natural and industrial Hg transformations. MIF of Hg isotopes is observed during abiotic reduction, photochemical and non-photochemical, and physical and chemical processes. Such processes lead to differences in the Hg isotopic composition of different emission sources, both natural and anthropogenic, and atmospheric processes (i.e., transportation, oxidation/reduction, deposition, and reemission). Therefore, Hg isotopic compositions could be used to trace the sources and processes of atmospheric Hg. For securing the reliability and accuracy of atmospheric Hg isotope data, the methods of collection, pretreatment, and isotopic measurement for Hg0(g) were developed to obtain high recovery yield of samples with no Hg isotopic fractionation during each

  15. Chemical and Oxygen Isotopic Composition of Roman and Late Antique Glass from Northern Greece

    Directory of Open Access Journals (Sweden)

    Alberta Silvestri


    Full Text Available The present paper emphasizes the importance of measuring the oxygen isotopic and chemical compositions of ancient glass, in order to constrain some features such as age, raw materials, and production technologies and to identify the “fingerprint” of local productions. In this context, thirty-nine Roman and late Antique glass samples and eight chert samples from northern Greece were selected and analysed for their oxygen isotopic and chemical compositions. Results show that the majority of glass samples are produced using natron as flux and have δ18O values of about 15.5‰, plus or minus a few tenths of one per mil, suggesting that raw materials probably come from Levantine area. Four samples are heavily enriched in 18O, and their chemical composition clearly shows that they were made with soda plant ash as flux. Isotopic and chemical data of Greek chert samples support the hypothesis of local production of the above samples. About half of the glass samples have chemical compositions, which allow their age to be constrained to the late Antique period. For the remaining glass, similarities with literature compositional groups are reported and discussed.

  16. A non-terrestrial 16O-rich isotopic composition for the protosolar nebula. (United States)

    Hashizume, Ko; Chaussidon, Marc


    The discovery in primitive components of meteorites of large oxygen isotopic variations that could not be attributed to mass-dependent fractionation effects has raised a fundamental question: what is the composition of the protosolar gas from which the host grains formed? This composition is probably preserved in the outer layers of the Sun, but the resolution of astronomical spectroscopic measurements is still too poor to be useful for comparison with planetary material. Here we report a precise determination of the oxygen isotopic composition of the solar wind from particles implanted in the outer hundreds of nanometres of metallic grains in the lunar regolith. These layers of the grains are enriched in 16O by >20 +/- 4 per thousand relative to the Earth, Mars and bulk meteorites, which implies the existence in the solar accretion disk of reactions--as yet unknown--that were able to change the 17O/16O and 18O/16O ratios in a way that was not dependent strictly on the mass of the isotope. Photochemical self-shielding of the CO gas irradiated by ultraviolet light may be one of these key processes, because it depends on the abundance of the isotopes, rather than their masses.

  17. The specific carbon isotopic compositions of branched and cyclic hydrocarbons from Fushun oil shale

    Institute of Scientific and Technical Information of China (English)

    DUAN Yi; WU Baoxiang; ZHENG Guodong; ZHANG Hui; ZHENG Chaoyang


    Various branched and cyclic hydrocarbons are isolated from the Fushun oil shale and their carbon isotopes are determined. The analytical results show that the branched and cyclic hydrocarbons are fully separated from n-alkanes by 5 A Molecular-sieve adduction using long time and cold solvent. The branched and cyclic hydrocarbon fraction obtained by this method is able to satisfy the analytic requests of GC-IRMS. The carbon isotopic compositions of these branched and cyclic hydrocarbons obtained from the sample indicate that they are derived from photoautotrophic algae, chemoautotrophic bacteria (-3.4‰ --39.0‰) and methanotrophic bacteria (-38.4‰--46.3‰). However the long-chain 2-methyl-branched alkanes indicate that their carbon isotopic compositions reflect biological origin from higher plants. The carbon isotopic composition of C30 4-methyl sterane (-22.1‰) is the heaviest in all studied ste- ranes, showing that the carbon source or growth condition for its precursor, dinoflagellate, may be different from that of regular steranes. The variation trend of δ13C values between isomers of hopanes shows that 13C-enriched precursors take precedence in process of their epimerization. Methanotrophic hopanes presented reveal the processes of strong transformation of organic matter and cycling of organic carbon in the water column and early diagenesis of oil shale.

  18. Stable carbon isotope composition of monoterpanes in essential oils and crude oils

    Institute of Scientific and Technical Information of China (English)


    Twenty-five monoterpanes from six types of essential oils and hydrogenated turpentine oil have been identified and their stable carbon isotope composition determined.Monoterpanes in essential oils sourced from terrestrial higher plants display a δ13C value in the range of-34‰-26‰,and mostly between-29‰ and-27‰.The δ13C value of any single monoterpane is very consistent in different essential oils.Acyclic monoterpanes show closer isotope composition between-28.6‰ and-26.2‰,with an average value of-27.7‰.In contrast,the isotope composition of cyclic monoterpanes is more scattered with an average value of-28.6‰.Isotopic fractionation with 13C enrichment has been observed during both artificial and geological hydrogenation of monoterpenoids to monoterpanes,and this is more obvious for the acyclic monoterpenoids.In addition to higher plants,acyclic monoterpane 2,6-dimethylheptane in crude oil can also be originated from other organic inputs.

  19. Preservation of Earth-forming events in the tungsten isotopic composition of modern flood basalts (United States)

    Rizo, Hanika; Walker, Richard J.; Carlson, Richard W.; Horan, Mary F.; Mukhopadhyay, Sujoy; Manthos, Vicky; Francis, Don; Jackson, Matthew G.


    How much of Earth's compositional variation dates to processes that occurred during planet formation remains an unanswered question. High-precision tungsten isotopic data from rocks from two large igneous provinces, the North Atlantic Igneous Province and the Ontong Java Plateau, reveal preservation to the Phanerozoic of tungsten isotopic heterogeneities in the mantle. These heterogeneities, caused by the decay of hafnium-182 in mantle domains with high hafnium/tungsten ratios, were created during the first ~50 million years of solar system history, indicating that portions of the mantle that formed during Earth’s primary accretionary period have survived to the present.

  20. The Oxygen Isotopic Composition of MIL 090001: A CR2 Chondrite with Abundant Refractory Inclusions (United States)

    Keller, Lindsay P.; McKeegan, K. D.; Sharp, Z. D.


    MIL 090001 is a large (>6 kg) carbonaceous chondrite that was classified as a member of the CV reduced subgroup (CVred) that was recovered during the 2009-2010 ANSMET field season [1]. Based on the abundance of refractory inclusions and the extent of aqueous alteration, Keller [2] suggested a CV2 classification. Here we report additional mineralogical and petrographic data for MIL 090001, its whole-rock oxygen isotopic composition and ion microprobe analyses of individual phases. The whole rock oxygen isotopic analyses show that MIL 090001 should be classified as a CR chondrite.

  1. On the iron isotope composition of Mars and volatile depletion in the terrestrial planets (United States)

    Sossi, Paolo A.; Nebel, Oliver; Anand, Mahesh; Poitrasson, Franck


    Iron is the most abundant multivalent element in planetary reservoirs, meaning its isotope composition (expressed as δ57Fe) may record signatures of processes that occurred during the formation and subsequent differentiation of the terrestrial planets. Chondritic meteorites, putative constituents of the planets and remnants of undifferentiated inner solar system bodies, have δ57Fe ≈ 0 ‰; an isotopic signature shared with the Martian Shergottite-Nakhlite-Chassignite (SNC) suite of meteorites. The silicate Earth and Moon, as represented by basaltic rocks, are distinctly heavier, δ57Fe ≈ + 0.1 ‰. However, some authors have recently argued, on the basis of iron isotope measurements of abyssal peridotites, that the composition of the Earth's mantle is δ57Fe = + 0.04 ± 0.04 ‰, indistinguishable from the mean Martian value. To provide a more robust estimate for Mars, we present new high-precision iron isotope data on 17 SNC meteorites and 5 mineral separates. We find that the iron isotope compositions of Martian meteorites reflect igneous processes, with nakhlites and evolved shergottites displaying heavier δ57Fe (+ 0.05 ± 0.03 ‰), whereas MgO-rich rocks are lighter (δ57Fe ≈ - 0.01 ± 0.02 ‰). These systematics are controlled by the fractionation of olivine and pyroxene, attested to by the lighter isotope composition of pyroxene compared to whole rock nakhlites. Extrapolation of the δ57Fe SNC liquid line of descent to a putative Martian mantle yields a δ57Fe value lighter than its terrestrial counterpart, but indistinguishable from chondrites. Iron isotopes in planetary basalts of the inner solar system correlate positively with Fe/Mn and silicon isotopes. While Mars and IV-Vesta are undepleted in iron and accordingly have chondritic δ57Fe, the Earth experienced volatile depletion at low (1300 K) temperatures, likely at an early stage in the solar nebula, whereas additional post-nebular Fe loss is possible for the Moon and angrites.

  2. Constraints from Os-isotope variations on the origin of Lena Trough abyssal peridotites and implications for the composition and evolution of the depleted upper mantle (United States)

    Lassiter, J. C.; Byerly, B. L.; Snow, J. E.; Hellebrand, E.


    The Lena Trough is a highly oblique, sparsely magmatic, ultra-slow spreading center located at the smallest distance between North America and Eurasia in the Arctic basin. Competing models suggest that it is either floored by oceanic mantle abyssal peridotites (APs) exposed by lithospheric necking, or by subcontinental mantle exposed in a still juvenile rift. To distinguish between these hypotheses, we have examined mineral major and trace element and whole rock Os-isotope variations in Lena Trough peridotites. Lena Trough peridotites are predominantly LREE-depleted, similar to other AP suites, and have 187Os/188Os ranging from ∼0.118 to 0.130 (Ave.=0.1244). This distribution is nearly identical to that of abyssal peridotites globally. Both the REE patterns and the Os-isotope distribution of the Lena Trough peridotites differ starkly from subcontinental mantle xenoliths sampled at Svalbard adjacent to Lena Trough. This suggests that Lena Trough is a site of oceanic spreading, although mid-ocean ridge volcanism as such has not yet begun. Highly refractory APs from several settings have Os- and Hf-isotope compositions indicating ancient (>1 Ga) melt depletion. Some researchers have proposed that at least some APs do not directly sample the convecting upper mantle source of MORB, but instead sample highly melt-depleted residues either entrained in the convecting mantle or present as a buoyant “slag” floating atop the less-depleted MORB-source mantle. However, ocean island peridotite xenoliths and APs reveal an essentially identical, non-Gaussian distribution of Os-isotopes and also span a similar range in Hf-isotopes. The similar mean and distribution of Os-isotopes between APs and ocean island xenoliths indicate that these two sample types derive from the same heterogeneous mantle reservoir. This similarity is inconsistent with the AP “slag hypothesis” due to the significantly greater depth of origin of ocean island xenoliths with respect to APs. Global

  3. Microstructure and properties of an HfB{sub 2}-SiC composite for ultra high temperature applications

    Energy Technology Data Exchange (ETDEWEB)

    Monteverde, F.; Bellosi, A. [National Research Council, Institute of Science and Technology for Ceramics, Via Granarolo 64, 48018 Faenza (Italy)


    An ultra-high-temperature ceramic (UHTC) based on HfB{sub 2} was produced. The microstructure consisted of fine and regular diboride grains (2 {mu}m average size), with SiC particulate distributed intergranularly, not rarely in clustered formation, and low levels of secondary phases were identified. The resulting thermo-mechanical properties proved interesting results for microhardness and fracture toughness. The microstructural alteration experienced within the explored temperature range renders the material unsuitable for service in extreme conditions of temperature and pressure. (Abstract Copyright [2004], Wiley Periodicals, Inc.)

  4. A Record of Oceanic Lithium Isotope Composition for the Last 7Ma (United States)

    Marriott, C. S.; Henderson, G. M.


    Continental weathering plays an important role in global climate change but has proved difficult to reconstruct for the past. New geological tools with which to assess the past rate and style of weathering are therefore urgently required. One such tool is Li isotope fractionation. Recent studies [1,2] have shown preferential release of 7Li into the aqueous phase and retention/adsorption of 6Li during weathering processes such as partial dissolution and secondary mineral formation. Lithium behaves conservatively in the oceans, with a residence time of ˜1Ma, so that a history of ocean Li isotope composition provides information about the average rate and style of global continental weathering on long timescales. The incorporation of lithium as a trace element in marine carbonates enables the construction of a record of oceanic Li-isotopic variation and is the focus of this work. Carbonate Li-isotope compositions are lighter than seawater by ˜8 per mil, but this fractionation is not temperature dependent. This has been demonstrated by measurement of Li isotopes in inorganically precipitated calcites (5-30° C) [3], in coralline aragonite (25-30° C) [3] and in benthic foraminifera Uvigerina (7-23° C). This lack of T-dependent fractionation suggests that the variation in the isotope composition of planktonic foraminifera will solely reflect changes in oceanic Li isotope composition, which in turn is strongly influence by changes in continental weathering. ODP site 758, located on the Ninetyeast Ridge in the Indian Ocean (5° N, 90° E; 2925m), was sampled at 2m intervals, over a depth corresponding to the last 7Ma, to produce 55 samples with a temporal resolution of approximately 130Ka. Site 758 is previously well studied with an existing chronology and high resolution Sr, O and Nd isotope data. Individual foram species in the core top were first investigated to assess inter-species fractionation effects. Down core lithium isotope variation was examined by

  5. Temperature and Oxygen Isotope Composition of The Ediacaran Ocean: Constraints From Clumped Isotope Carbonate Thermometry (United States)

    Bonifacie, M.; Eiler, J. M.; Fike, D. A.


    The temperature and chemical variations of the early oceans on Earth are highly debated, particularly for periods associated with significant evolutionary change and/or extinction. The temperature of past oceans has been estimated based on conventional carbonate-water and/or silicate-water stable oxygen isotope thermometry. Precambrian carbonates and silicates both exhibit a long-term secular trend of increasing δ18O values with decreasing age. This trend has been used to support two opposite - though related - interpretations: the Earth's oceans gradually cooled over the course of the Proterozoic eon, from a maximum of ~ 60-90°C at ~ 2.5Ga (and were, on average, relatively warm during much of the Paleozoic era) [1]. This interpretation has been supported by Si-isotope proxies and the thermal tolerances of proteins in various classes of microbial organisms [2-3]. Alternatively, the δ18O value of the oceans has gradually increased through time [4-5], and mean Earth surface temperatures varied over a narrow range similar to modern conditions. In other terms, one either assumes an ocean of constant δ18O and infers that climate varied dramatically, or vise versa. Finally, it is possible that post- depositional processes (e.g., diagenesis, burial metamorphism, weathering) has modified the δ18O values of all or most Precambrian sedimentary carbonates and silicates, overprinting any paleoclimatic variations. Carbonate 'clumped isotope' thermometry provides a new way to independently test these hypotheses because it allows one to determine the apparent growth temperatures of carbonate minerals based on their abundances of 13C-18O bonds, as reflected by the 'Δ47' value of CO2 extracted by phosphoric acid digestion [6]. This method is thermodynamically based and independent of the δ18O of water from which the carbonate grew. We will report the initial results of measurements of 'Δ47 for a suite of carbonates from the Sultanate of Oman. This Ediacaran age (~ 635 to

  6. Change of Sm-Nd isotope composition during weathering of till (United States)

    Öhlander, Björn; Ingri, Johan; Land, Magnus; Schöberg, Hans


    Weathering of till in northern Sweden results in the formation of well-developed spodosols. The till is dominated by 1.9-1.8 Ga granitic material. The REE are among the elements most strongly depleted during weathering, and the loss of REE from the E-horizon decreases as the atomic number increases. To study if weathering leads to a change of the Nd isotope composition, we have analysed the Nd isotopic composition of the various horizons including living plants and humus of two profiles of weathered till (typic haplocryods) in northern Sweden. As much as between 65.6 and 75.3% of the Sm and Nd in the fraction has been lost from the E-horizon, and between 32.5 and 54.7% from the B-horizon. Nd has been lost to a slightly greater extent than Sm. The two C-horizon samples have ɛ Nd(0) values of -22.1 and -23.2. Corresponding E-horizon values are -18.1 and -20.2. The B-horizon values are intermediate between the values of the E and C horizons. It is concluded that the weathering leads to a change in the Sm/Nd ratio resulting in a change of the Sm-Nd isotope composition. The plant and humus samples deviate even more from the unweathered till. For one station the results could be interpreted as if the Sm and Nd taken up by the plants had similar isotope characteristics as the amounts of these elements released by weathering in the E-horizon. For the other station it is probable that the Nd isotope composition of the organic samples is dominated by Nd released by till weathering which, however, is mixed with another Nd-source, possibly an airborne component. The explanation to the change of isotope compostion in the till is that a larger proportion of the Nd released by weathering is released from minerals with a lower Sm/Nd ratio than the bulk soil, compared with the amount released from minerals with a higher Sm/Nd ratio. Although the various REE-carrying minerals had the same initial Nd isotopic composition, 1.8-1.9 Ga of decay of 147Sm to 143Nd has resulted in a

  7. Mesozoic Bimodal Volcanic Suite in Zhalantun of the Da Hinggan Range and Its Geological Significance:Zircon U-Pb Age and Hf Isotopic Constraints

    Institute of Scientific and Technical Information of China (English)


    Mesozoic bimodal volcanic rocks of basaltic andesite and rhyolite are widely distributed in the Da Hinggan Range, but their petrogenetic relationships and geodynamic implications are rarely constrained. Detailed studies on doleritic and porphyry dikes in the Zhalantun area indicate that they display features of magma mixing, suggesting their coeval formation. In situ zircon U-Pb dating shows that the porphyry was emplaced in the Early Cretaceous with a 206Pb/238U age of 130±1 Ma. Zircons from the dolerite also yield an Early Cretaceous emplacement age of 124±2 Ma although some inherited zircons have been identified. These age results indicate that the Early Cretaceous was an important period of magmatism in the Da Hinggan Range. Zircons from porphyry are characterized by positive value of εHf(t) as high as 10.3±0.5 with Hf depleted mantle model age of 349-568 Ma, whereas magmatic zircons from the dolerite have εHf(t) value of 11.0±1.4 with Hf depleted mantel model age of 342-657 Ma,consistent with those from the porphyry. Considering other data on the geological evolution of this area,it is concluded that the mafic magma originated from the partial melting of Paleozoic enriched lithospheric mantle, whereas the felsic magma came from recycling of juvenile crust formed during the Paleozoic. Both of the protoliths are closely related to the subduction of the Paleo-Asian Ocean during the Paleozoic, indicating that the Paleozoic is an important period of large-scale crustal growth in the area.

  8. Predicting the Isotopic Composition of Subduction-Filtered Subducted Oceanic Crust and Sediment (United States)

    White, W. M.


    The chemical and isotopic character of mantle plumes, which produce oceanic island volcanoes, are widely thought to reflect the presence of recycled oceanic crust and sediment. Isotopic systematics suggest the “cycle time” for this process is 1 Ga or longer, but it should be possible to use a simple mass balance approach to discern how the presently operating subduction zone filter affects the ratios of radioactive parent to radiogenic daughter isotopes. Simple uniformitarian assumptions can then be used to predict the present isotopic composition of anciently subducted lithosphere. Our underlying assumption in deciphering the subduction zone filter is that the flux of an element into the deep mantle is simply equal to the flux of element into the subduction zone less the flux of that element into subduction zone magmas. The former is readily calculated from published data. The latter can be calculated by estimating parental magma compositions, arc accretion rates, and the assumption that arc magma compositions differ from MORB only because of material derived from subducting crust and sediment. Using this approach for 8 intra-oceanic subduction zones, we find 73% of Th and Pb, 79% of U, 80% of Rb and Sr, 93% of Nd and 98% of Sm survive the subduction zone filter. The subduction zone filter systematically increases Sm/Nd ratios in all subduction zones, but the effect is small, with a weighted mean increase of 1.5%. The effect of subduction is to decrease the Sm/Nd of the mantle, but only slightly. The effect of subduction is to increase the Rb/Sr of the mantle, but the subduction zone filter does not have a systematic effect on Rb/Sr ratios: it significantly increases in Rb/Sr in 3 subduction zones and significantly decreases it in one; the weighted mean shows no significant change. The effect of the subduction zone filter on U/Pb is also not systematic. U/Pb ratios in the mantle fluxes are bimodal, with values equal to or lower than the bulk Earth value in 4

  9. Stable isotope and chemical compositions of European and Australasian ciders as a guide to authenticity. (United States)

    Carter, James F; Yates, Hans S A; Tinggi, Ujang


    This paper presents a data set derived from the analysis of bottled and canned ciders that may be used for comparison with suspected counterfeit or substitute products. Isotopic analysis of the solid residues from ciders (predominantly sugar) provided a means to determine the addition of C4 plant sugars. The added sugars were found to comprise cane sugar, high-fructose corn syrup, glucose, or combinations. The majority of ciders from Australia and New Zealand were found to contain significant amounts of added sugar, which provided a limited means to distinguish these ciders from European ciders. The hydrogen and oxygen isotopic compositions of the whole ciders (predominantly water) were shown to be controlled by two factors, the water available to the parent plant and evaporation. Analysis of data derived from both isotopic and chemical analysis of ciders provided a means to discriminate between regions and countries of manufacture.

  10. Modelling the regional climate and isotopic composition of Svalbard precipitation using REMOiso

    DEFF Research Database (Denmark)

    Divine..[], D.V.; Sjolte, Jesper; Isaksson, E.;


    Simulations of a regional (approx. 50 km resolution) circulation model REMOiso with embedded stable water isotope module covering the period 1958-2001 are compared with the two instrumental climate and four isotope series (d18O) from western Svalbard. We examine the data from ice cores drilled...... on Svalbard ice caps in 1997 (Lomonosovfonna, 1250 m asl) and 2005 (Holtedahlfonna, 1150 m asl) and the GNIP series from Ny-angstrom lesund and Isfjord Radio. The surface air temperature (SAT) and precipitation data from Longyearbyen and Ny-angstrom lesund are used to assess the skill of the model...... in reproducing the local climate. The model successfully captures the climate variations on the daily to multidecadal times scales although it tends to systematically underestimate the winter SAT. Analysis suggests that REMOiso performs better at simulating isotope compositions of precipitation in the winter...

  11. Carbon isotope composition of low molecular weight hydrocarbons and monocarboxylic acids from Murchison meteorite (United States)

    Yuen, G.; Blair, N.; Des Marais, D. J.; Chang, S.


    Carbon isotopic compositions have been measured for individual hydrocarbons and monocarboxylic acids from the Murchison meteorite, a C2 carbonaceous chondrite which fell in Australia in 1969. With few exceptions, notably benzene, the volatile products are substantially isotopically heavier than their terrestrial counterparts, signifying their extraterrestrial origin. For both classes of compounds, the ratio of C-13 to C-12 decreases with increasing carbon number in a roughly parallel manner, and each carboxylic acid exhibits a higher isotopic ratio than the hydrocarbon containing the same number of carbon atoms. These trends are consistent with the kinetically controlled synthesis of higher homologues from lower ones. The results suggest the possibility that the production mechanisms for hydrocarbons and carboxylic acids may be similar, and impose constraints on the identity of the reactant species.

  12. Absolute isotopic composition and atomic weight of neodymium using thermal ionization mass spectrometry. (United States)

    Zhao, Motian; Zhou, Tao; Wang, Jun; Lu, Hai; Fang, Xiang; Guo, Chunhua; Li, Qiuli; Li, Chaofeng


    Synthetic mixtures prepared gravimetrically from highly enriched isotopes of neodymium in the form of oxides of well-defined purity were used to calibrate a thermal ionization mass spectrometer. A new error analysis was applied to calculate the final uncertainty of the atomic weight value. Measurements on natural neodymium samples yielded an absolute isotopic composition of 27.153(19) atomic percent (at.%) 142Nd, 12.173(18) at.% 143Nd, 23.798(12) at.% 144Nd, 8.293(7) at.% 145Nd, 17.189(17) at.% 146Nd, 5.756(8) at.% 148Nd, and 5.638(9) at.% 150Nd, and the atomic weight of neodymium as 144.2415(13), with uncertainties given on the basis of 95% confidence limits. No isotopic fractionation was found in terrestrial neodymium materials.

  13. Stable isotope study of a new chondrichthyan fauna (Kimmeridgian, Porrentruy, Swiss Jura): an unusual freshwater-influenced isotopic composition for the hybodont shark Asteracanthus (United States)

    Leuzinger, L.; Kocsis, L.; Billon-Bruyat, J.-P.; Spezzaferri, S.; Vennemann, T.


    Chondrichthyan teeth (sharks, rays, and chimaeras) are mineralized in isotopic equilibrium with the surrounding water, and parameters such as water temperature and salinity can be inferred from the oxygen isotopic composition (δ18Op) of their bioapatite. We analysed a new chondrichthyan assemblage, as well as teeth from bony fish (Pycnodontiformes). All specimens are from Kimmeridgian coastal marine deposits of the Swiss Jura (vicinity of Porrentruy, Ajoie district, NW Switzerland). While the overall faunal composition and the isotopic composition of bony fish are generally consistent with marine conditions, unusually low δ18Op values were measured for the hybodont shark Asteracanthus. These values are also lower compared to previously published data from older European Jurassic localities. Additional analyses on material from Solothurn (Kimmeridgian, NW Switzerland) also have comparable, low-18O isotopic compositions for Asteracanthus. The data are hence interpreted to represent a so far unique, freshwater-influenced isotopic composition for this shark that is classically considered a marine genus. While reproduction in freshwater or brackish realms is established for other hybodonts, a similar behaviour for Asteracanthus is proposed here. Regular excursions into lower salinity waters can be linked to the age of the deposits and correspond to an ecological adaptation, most likely driven by the Kimmeridgian transgression and by the competition of the hybodont shark Asteracanthus with the rapidly diversifying neoselachians (modern sharks).

  14. Stable isotope study of a new chondrichthyan fauna (Kimmeridgian, Porrentruy, Swiss Jura: an unusual freshwater-influenced isotopic composition for the hybodont shark Asteracanthus

    Directory of Open Access Journals (Sweden)

    L. Leuzinger


    Full Text Available Chondrichthyan teeth (sharks, rays and chimaeras are mineralised in isotopic equilibrium with the surrounding water, and parameters such as water temperature and salinity can be inferred from the oxygen isotopic composition (δ18Op of their bioapatite. We analysed a new chondrichthyan assemblage, as well as teeth from bony fish (Pycnodontiformes. All specimens are from Kimmeridgian coastal marine deposits of the Swiss Jura (vicinity of Porrentruy, Ajoie district, NW Switzerland. While the overall faunal composition and the isotopic composition of bony fish are consistent with marine conditions, unusually low δ18Op values were measured for the hybodont shark Asteracanthus. These values are also lower compared to previously published data from older European Jurassic localities. Additional analyses on material from Solothurn (Kimmeridgian, NW Switzerland also have comparable, low-18O isotopic compositions for Asteracanthus. The data are hence interpreted to represent a so far unique, freshwater-influenced isotopic composition for this shark that is classically considered as a marine genus. While reproduction in freshwater or brackish realms is established for other hybodonts, a similar behaviour for Asteracanthus is proposed here. Regular excursions into lower salinity waters can be linked to the age of the deposits and correspond to an ecological adaptation, most likely driven by the Kimmeridgian transgression and by the competition of the primitive shark Asteracanthus with the rapidly diversifying neoselachians (modern sharks.

  15. Experimental assessment of environmental influences on the stable isotopic composition of Daphnia pulicaria and their ephippia (United States)

    Schilder, J.; Tellenbach, C.; Möst, M.; Spaak, P.; van Hardenbroek, M.; Wooller, M. J.; Heiri, O.


    The stable isotopic composition of fossil resting eggs (ephippia) of Daphnia spp. is being used to reconstruct past environmental conditions in lake ecosystems. However, the underlying assumption that the stable isotopic composition of the ephippia reflects the stable isotopic composition of the parent Daphnia, of their diet and of the environmental water have yet to be confirmed in a controlled experimental setting. We performed experiments with Daphnia pulicaria cultures, which included a control treatment conducted at 12 °C in filtered lake water and with a diet of fresh algae, and three treatments in which we manipulated the stable carbon isotopic composition (δ13C value) of the algae, stable oxygen isotopic composition (δ18O value) of the water, and the water temperature, respectively. The stable nitrogen isotopic composition (δ15N value) of the algae was similar for all treatments. At 12 °C, differences in algal δ13C values and in δ18O values of water are reflected in those of Daphnia. The differences between ephippia and Daphnia stable isotope ratios were similar in the different treatments (δ13C: + 0.2 ± 0.4‰ (SD); δ15N: -1.6 ± 0.4‰; δ18O: -0.9 ± 0.4‰) indicating that changes in dietary δ13C and δ18O values of water are passed on to these fossilizing structures. A higher water temperature (20 °C) resulted in lower δ13C values in Daphnia and ephippia than in the other treatments with the same food source and in a minor change in the difference between δ13C values of ephippia and Daphnia (to -1.3 ± 0.3‰). This may have been due to microbial processes or increased algal respiration rates in the experimental containers, which may not affect Daphnia in natural environments. There was no significant difference in the offset between δ18O and δ15N values of ephippia and Daphnia between the 12 °C and 20 °C treatments, but the δ18O values of Daphnia and ephippia were on average 1.2‰ lower at 20 °C compared with 12 °C. We conclude

  16. Lead isotopic compositions of common arsenical pesticides used in New England (United States)

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


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

  17. Soil Drying Effects on the Carbon Isotope Composition of Soil Respiration (United States)

    Phillips, C. L.; Nickerson, N.; Risk, D.; Kayler, Z. E.; Rugh, W.; Mix, A. C.; Bond, B. J.


    Stable isotopes are used widely as a tool for determining sources of carbon (C) fluxes in ecosystem C studies. Environmental factors that change over time, such as moisture, can create dynamic changes in the isotopic composition of C assimilated by plants, and offers a unique opportunity to distinguish fast- responding plant C from slower-responding soil C pools, which under steady-state conditions may be too similar isotopically to partition. Monitoring the isotopic composition of soil respiration over a period of changing moisture conditions is potentially a useful approach for characterizing plant contributions to soil respiration. But this partitioning hinges on the assumption that any change in the isotopic signature of soil respiration is solely due to recent photosynthetic discrimination, and that post-photosynthetic processes, such as microbial respiration, do not discriminate as moisture decreases. The purpose of the present study is to test the assumption that δ13CO2 from microbial respiration remains static as soil dries. We conducted a series of greenhouse experiments employing different techniques to isolate microbial respiration from root respiration. The first involves removing roots from soil, and showed that when roots are present, respiration from dry soil is enriched in 13C relative to moist soil, but when roots are absent, respiration is isotopically similar from moist and dry soils. This indicates that rhizospheric respiration changes isotopically with moisture whereas soil microbial respiration does not. In contrast, a second experiment in which soil columns without plants were monitored as they dried, showed respiration from very dry soil to be enriched by 8‰ relative to moist soil. However, simulations with an isotopologue-based soil gas diffusion model demonstrate that at least a portion of the apparent enrichment is due to non-steady state gas transport processes. Careful sampling methodologies which prevent or account for non

  18. REE characteristics and Pb, Sr and Nd isotopic compositions of steel plant emissions. (United States)

    Geagea, M Lahd; Stille, P; Millet, M; Perrone, Th


    A comprehensive Pb-Sr-Nd isotope and REE tracer study of atmospheric trace metal pollution by a steel plant situated to the north of the urban communities of Strasbourg (France) and Kehl (Germany) has been performed using tree barks as biomonitors. The 206Pb/207Pb and 208Pb/207Pb isotopic ratios of the steel plant's filter dust are similar to values found in dust of waste incinerators. The 87Sr/86Sr ratio is similar to present-day ratios of Phanerozoic or Precambrian granitic rocks. The 143Nd/144Nd isotopic composition is very low and corresponds to an (Nd) value of -17.5. Such a low value is characteristic of old Precambrian granitic rocks and banded iron formations. Thus, this low (Nd) value might point to the origin of the iron necessary for the steel production. The fact, that this isotopic composition does not occur in crustal rocks of Western Central Europe makes the Nd isotope ratio a powerful tool to trace steel plants atmospheric emissions. The rare earth element (REE) distribution pattern of the steel plant's filter dust shows very specific fractionations like La and Nd enrichments which are traceable in tree barks over a distance of 4 km. The Pb, Sr and Nd isotope ratios not only enable the steel plant's emissions to be traced in a north-easterly direction, along the principal wind pathway but also enables the interference of this emission at 4 km NE from the steel plant with another atmospheric component originating from the Strasbourg Rhine harbour to be identified.

  19. Detection of phosphohydrolytic enzyme activity through the oxygen isotope composition of dissolved phosphate (United States)

    Colman, A. S.


    Phosphohydrolytic enzymes play an important role in phosphorus remineralization. As they release phosphate (Pi) from various organophosphorus compounds, these enzymes facilitate the transfer of oxygen atoms from water to the phosphoryl moieties. Most such enzymatic reactions impart a significant isotopic fractionation to the oxygen transferred. If this reaction occurs within a cell, then the resultant oxygen isotope signal is overprinted by continued recycling of the Pi. However, if this reaction occurs extracellularly, then the isotopic signal will be preserved until the Pi is transported back into a cell. Thus, the oxygen isotope composition of Pi (δ18Op) in an aquatic ecosystem can serve as a useful indicator of the mechanisms by which P is remineralized. We develop a time-dependent model illustrating the sensitivity of the δ18O of dissolved phosphate to various modes of P remineralization. The model is informed by cell lysis experiments that reveal the relative proportions of P­i that are directly liberated from cytosol vs. regenerated from co-liberated dissolved organic phosphorus compounds via extracellular hydrolysis. By incorporating both cellular uptake and release fluxes of P, we show that the degree of isotopic disequilibrium in an aquatic ecosystem can be a strong indicator of P remineralization mode. Apparent oxygen isotope equilibrium between Pi and water arises in this model as a steady-state scenario in which fractionation upon cellular uptake of Pi counterbalances the hydrolytic source flux of disequilibrated Pi. Low and high rates of extracellular phosphohydrolase activity are shown to produce steady-state δ18Op values that are respectively above or below thermodynamic equilibrium compositions.

  20. Diamond growth history from in situ measurement of Pb and S isotopic compositions of sulfide inclusions (United States)

    Rudnick, Roberta L.; Eldridge, C. Stewart; Bulanova, Galina P.


    In a continuing effort to understand crust-mantle dynamics, we have determined the S and Pb isotopic compositions of mantle sulfides encapsulated within diamonds from under the Siberian craton and compared these results to those of previously investigated African counterparts. Because diamond inclusions are isolated from exchange with surrounding mantle, they may preserve the history of diamond growth and act as direct tracers of the origins of mantle materials. Study of these inclusions may thus offer the best chance of recognizing global-scale interaction between Earth's crust and mantle. Although δ34S values of the Siberian sulfides do not deviate significantly from the mantle value of 0‰ ± 3‰, Pb isotopic compositions are highly variable. Pb isotopic compositions of sulfides from peridotitic suite diamonds generally plot near the terrestrial Pb growth curve, with model ages ranging between 0 and 2 Ga, whereas sulfides from eclogitic suite diamonds have radiogenic compositions, plotting beyond the growth curve. These results, which are similar to those for sulfides in African diamonds, suggest that the sulfides from eclogitic suite diamonds were derived from a source with an unusually high U/Pb ratio and may indicate a common process (such as subduction of crystal materials into the mantle) operating beneath Africa and Siberia. The absence of extremely radiogenic Pb in sulfides from eclogite xenoliths suggests that the radiogenic material from which eclogitic suite diamonds grew was a transient feature of the mantle, associated with diamond growth. The ultimate origin of this high U/Pb signature, however, remains enigmatic. Large variations in Pb isotopic composition of sulfides from different zones in a single peridotitic suite diamond document (1) crystallization of the diamond's core near 2.0 Ga, (2) growth of its outer zone in an environment with a high U/Pb ratio similar to the growth environment of eclogitic suite diamonds, and (3) growth of the

  1. Promise and Pitfalls of Lu/Hf-Sm/Nd Garnet Geochronology (United States)

    King, R. L.; Vervoort, J. D.; Kohn, M. J.; Zirakparvar, N. A.; Hart, G. L.; Corrie, S. L.; Cheng, H.


    Our ability to routinely measure Lu-Hf and Sm-Nd isotopes in garnet allows broad new applications in geochronology, petrology, and tectonics. However, applications of these data can be limited by challenges in interpreting the petrologic record and preparing garnets for analysis. Here, we examine petrologic and chemical pitfalls encountered in garnet geochronology. Petrologic factors influencing trace element compositions in garnet include reactions that modify REE availability and partitioning (1,2), kinetically limited transfer of REEs to garnet (3), and bulk compositional heterogeneities (4). Interpreting the effects of these processes on Sm/Nd and Lu/Hf ages requires characterizing REE zonation prior to isotope analysis and age interpretation. Because garnet fractions are traditionally picked from crushed samples without regard to intracrystalline origins or chemistries, isochrons will represent mixtures derived to varying degrees from all periods of garnet growth. While measured zoning might generally indicate what garnet portion dominates the Lu/Hf or Sm/Nd budget, traditional mineral separation will rarely realize the chronologic potential afforded by high precision Hf and Nd isotope measurements. The potential use of alternative techniques, such as microsampling, necessitates selective digestion and/or leaching to eliminate inclusions within garnet. For Sm/Nd geochronology, H2SO4 leaching removes LREE-rich phosphates (e.g. apatite), but not silicates (e.g. epidote), precluding Sm-Nd dating of some rocks. For Lu/Hf geochronology, ubiquitous zircon microinclusions (c. 1 μm) can significantly disrupt age determinations. Microinclusions cannot be detected optically or separated physically, requiring selective chemical digestion. If complete digestion methods, such as bomb digestion, are used for garnet fractions, then "common Hf" from zircon will be contained in final solutions. These mixed analyses are of dubious utility and will fall into one of two

  2. Isotope composition of winter precipitation and snow cover in the foothills of the Altai

    Directory of Open Access Journals (Sweden)

    N. S. Malygina


    Full Text Available Over the past three decades, several general circulation models of the atmosphere and ocean (atmospheric and oceanic general circulation models  – GCMs have been improved by modeling the hydrological cycle with the use of isotopologues (isotopes of water HDO and H2 18O. Input parameters for the GCM models taking into account changes in the isotope composition of atmospheric precipitation were, above all, the results obtained by the network GNIP – Global Network of Isotopes in Precipitation. At different times, on the vast territory of Russia there were only about 40 simultaneously functioning stations where the sampling of atmospheric precipitation was performed. In this study we present the results of the isotope composition of samples taken on the foothills of the Altai during two winter seasons of 2014/15 and 2015/16. Values of the isotope composition of precipitation changed in a wide range and their maximum fluctuations were 25, 202 and 18‰ for δ18О, dexc and δD, respectively. The weighted-mean values of δ18О and δD of the precipitation analyzed for the above two seasons were close to each other (−21.1 and −158.1‰ for the first season and −21.1 and −161.9‰ for the second one, while dexc values differed significantly. The compa