SHRIMP U–Pb ages of diagenetic and hydrothermal xenotime from the Archaean Witwatersrand Supergroup of South Africa     

Gavin L. England  Birger Rasmussen  Neal J. McNaughton  Ian R. Fletcher  David I. Groves  & Bryan Krapez 《地学学报》2001,13(5):360-367

SHRIMP dating of xenotime overgrowths on detrital zircon grains can constrain maximum durations since diagenesis and therefore provide minimum dates of sediment deposition. Thus, xenotime dating has significant economic application to Precambrian sediment-hosted ore deposits, such as Witwatersrand Au–U, for which there are no precise depositional ages. The growth history of xenotime in the Witwatersrand Supergroup is texturally complex, with several phases evident. The oldest authigenic xenotime ²⁰⁷Pb/²⁰⁶Pb age obtained in sandstone underlying the Vaal Reef is 2764 ± 5 Myr (1 σ), and most likely represents a mixture of diagenetic and hydrothermal growth. Nevertheless, this represents the oldest authigenic mineral age yet recorded in the sequence and provides a minimum age of deposition. Other xenotime data record a spread of ages that correspond to numerous post-diagenetic thermotectonic events (including a Ventersdorp event at ≈ 2720 Ma) up to the ≈2020 Ma Vredefort event.  相似文献   

On the Spatial Distribution and Seasonal Variation of Lower-Troposphere Ozone over Europe     

H. E. Scheel  H. Areskoug  H. Geiss  B. Gomiscek  K. Granby  L. Haszpra  L. Klasinc  D. Kley  T. Laurila  A. Lindskog  M. Roemer  R. Schmitt  P. Simmonds  S. Solberg  G. Toupance 《Journal of Atmospheric Chemistry》1997,28(1-3):11-28

Surface ozone data from 25 Europeanlow-altitude sites and mountain sites located between79°N and 28°N were studied. The analysiscovered the time period March 1989–February 1993.Average summer and winter O₃ concentrations inthe boundary layer over the continent gave rise togradients that were strongest in the north-west tosouth-east direction and west-east direction, respectively. WintertimeO₃ ranged from 19 to 27 ppbover the continent, compared to about 32 ppb at thewestern border, while for summer the continentalO₃ values ranged between 39 and 56 ppb and theoceanic mixing ratios were around 37 ppb. In the lowerfree troposphere average wintertime O₃ mixingratios were around 38 ppb, with only an 8 ppbdifference between 28°N and 79°N. For summerthe average O₃ levels decreased from about 55 ppbover Central Europe to 32 ppb at 79°N. Inaddition, O₃ and O_x(= O₃ + NO₂)in polluted and clean air were compared. Theamplitudes of the seasonal ozone variations increasedin the north-west to south-east direction, while thetime of the annual maximum was shifted from spring (atthe northerly sites) to late summer (at sites inAustria and Hungary), which reflected the contributionof photochemical ozone production in the lower partsof the troposphere.  相似文献   

Reactive Nitrogen Compounds at Spitsbergen in the Norwegian Arctic     

S. Solberg  T. Krognes  F. Stordal  OØ Hov  H. J. Beine  D. A. Jaffe  K. C. Clemitshaw  S. A. Penkett 《Journal of Atmospheric Chemistry》1997,28(1-3):209-225

Simultaneousindependent measurements of NO_y and NO_x(NO_x= NO + NO₂) by high-sensitivitychemiluminescence systems and of PAN (peroxyacetylnitrate) and PPN (peroxypropionyl nitrate) by GC-ECDwere made at Spitsbergen in the Norwegian Arcticduring the first half year of 1994. The average mixingratio of the sum of PAN and PPN (denoted PANs)increased from around 150 pptv in early winter to amaximum of around 500 pptv in late March, whereasepisodic peak values reached 800 pptv. This occurredsimultaneously with a maximum in ozone which increasedto 45–50 ppbv in March–April. The average NO_xmixing ratio was 27 pptv and did not show any cyclethrough the period. The NO_y mixing ratio showeda maximum in late March, while the difference betweenNO_y and PAN decreased during spring. This is anindication of the dominance of PAN in the NO_ybudget in the Arctic, but possible changes in theefficiency of the NO_y converter could alsocontribute to this. Although most PAN in theArctic is believed to be due to long range transport,the observations indicate local loss and formationrates of up to 1–2 pptv h^-1 in April–May.Measurements of carbonyl compounds suggest thatacetaldehyde was the dominant, local precursor ofPAN.Now at 1.  相似文献   

Greenhouse Gas Emissions and Costs over the Life Cycle of Wood and Alternative Flooring Materials     

Ann Kristin Petersen  Birger Solberg 《Climatic change》2004,64(1-2):143-167

Increased use of wood can substitute more energy demanding products and thus contribute to a long-term solution to the global warming problem. The aim of this article is to provide an empirical study on this substitution impact, its cost-effectiveness, and which methodological assumptions that are of highest importance for the results obtained. We have made a case study where we compare use of various flooring materials. The results show that floor covering in solid oak causes lower greenhouse gas (GHG) emissions than the other materials. The difference can be ranked in the following order, after their potential for reduction in GHG emissions: Carpet in wool, carpet in polyamide, vinyl, and linoleum. At 2% pro anno discount rate, the avoided GHG emission in tons per m³ of oak flooring used is 0.1–1.9 for linoleum, and 11.8–15.5 for wool carpets. Unless the solution in solid oak is on total less expensive over the lifetime of the building, only the price of avoided emissions from a substitution between solid oak and carpet in wool is reasonable, compared to present carbon fees. The assumptions that influence the result most are choice of discount rate, carbon fixation on forest area, and waste handling. Empirical case studies like this indicate GHG emission reduction potentials caused by substitution, but should be complemented by dynamic input/output analyses and econometric studies. To analyse the flow of CO₂ over time, they should also be linked to forest management models.  相似文献   

Olivine phenocrysts of Hawaiian olivine tholeiite and oceanite   总被引：4，自引：0，他引：4  

Sven Maaløe  Birger Hansen 《Contributions to Mineralogy and Petrology》1982,81(3):203-211

Olivine phenocrysts of Hawaiian tholeiites display a variety of textures and a variation in composition which is due to supercooled crystallization. The highest forsterite content measured is 91%, and the highest magnesia content estimated for a tholeiitic liquid is 17%, using the olivine geothermometer. The liquid of this composition may be either a primary magma or a primitive magma. It is not yet possible to specify any particular composition range for the primary Hawaiian tholeiites.  相似文献   

Boundary-layer ozone depletion as seen in the Norwegian Arctic in spring     

Sverre Solberg  Norbert Schmidbauer  Arne Semb  Frode Stordal  Øystein Hov 《Journal of Atmospheric Chemistry》1996,23(3):301-332

Several years of measurements of ozone, hydrocarbons, sulphate and meteorological parameters from Spitsbergen in the Norwegian Arctic are presented. Most of the measurements were taken on the Zeppelin Mountain at an altitude of 474 m a.s.l. The focus is the episodes of ozone depletion in the lower troposphere in spring, which are studied in a climatological way. Episodes of very low ozone concentrations are a common feature on the Zeppelin Mountain in spring. The low ozone episodes were observed from late March to the beginning of June. When the effect of transport direction was subtracted, the frequenty of the low ozone episodes was found to peak in the beginning of May, possibly reflecting the seasonal cycle in the actual depletion process. Analyses based on trajectory calculations show that most of the episodes occurred when the air masses were transported from W-N. Ozone soundings show that the ozone depletion may extend from the surface and up to 3–4 km altitude. The episodes were associated with a cold boundary layer beneath a thermally stable layer, suppressing mixing with the free troposphere. The concentration of several individual hydrocarbons was much lower during episodes of low ozone than for the average conditions. The change in concentration ratio between the hydrocarbons was in qualitative agreement with oxidation of hydrocarbons by Br and Cl atoms rather than by OH radicals.  相似文献   

Chemical Mechanism Development: Laboratory Studies and Model Applications     

Harald Geiger  Ian Barnes  Karl H. Becker  Birger Bohn  Theo Brauers  Birgit Donner  Hans-Peter Dorn  Manfred Elend  Carlos M. Freitas Dinis  Dirk Grossmann  Heinz Hass  Holger Hein  Axel Hoffmann  Lars Hoppe  Frank Hülsemann  Dieter Kley  Björn Klotz  Hans G. Libuda  Tobias Maurer  Djuro Mihelcic  Geert K. Moortgat  Romeo Olariu  Peter Neeb  Dirk Poppe  Lars Ruppert  Claudia G. Sauer  Oleg Shestakov  Holger Somnitz  William R. Stockwell  Lars P. Thüner  Andreas Wahner  Peter Wiesen  Friedhelm Zabel  Reinhard Zellner  Cornelius Zetzsch 《Journal of Atmospheric Chemistry》2002,42(1):323-357

Within the German Tropospheric Research Programme (TFS) numerous kinetic and mechanistic studies on the tropospheric reaction/degradation of the following reactants were carried out: oxygenated VOC, aromatic VOC, biogenic VOC, short-lived intermediates, such as alkoxy and alkylperoxy radicals.At the conception of the projects these selected groups were classes of VOC or intermediates for which the atmospheric oxidation mechanisms were either poorly characterised or totally unknown. The motivation for these studies was the attainment of significant improvements in our understanding of the atmospheric chemical oxidation processes of these compounds, particularly with respect to their involvement in photooxidant formation in the troposphere. In the present paper the types of experimental investigations performed and the results obtained within the various projects are briefly summarised. The major achievements are highlighted and discussed in terms of their contribution to improving our understanding of the chemical processes controlling photosmog formation in the troposphere.  相似文献   

Pyrite: physical and chemical textures   总被引：9，自引：0，他引：9  

J. R. Craig  F. M. Vokes  T. N. Solberg 《Mineralium Deposita》1998,34(1):82-101

Pyrite may crystallize initially in forms as diverse as framboids or cubes depending upon the temperatures and pressures. Fluid-rich diagenesis or low-grade metamorphism clearly results in thorough recrystallization and the common formation of cubes. Once these have formed, the pyrite becomes much more refractory and retains many characteristics even in deposits which have undergone penetrative deformation. This is in strong contrast to the behavior of most of the accompanying sulfides, which often undergo ductile deformation, solid state or chemical remobilization, and annealing. Pyrite deforms sparingly until there is brittle failure; however, there may be significant pyrite corrosion and regrowth during metamorphism as the result of sulfur exchange with other minerals, especially pyrrhotite. Pyrite fabrics may also be significantly modified by pressure solution or Coble creep. Optical microscopic examination and electron microprobe chemical mapping of pyrites from a variety of mineral deposits, including several high-grade metamorphic ones, reveals that the pyrites frequently contain both physical and chemical textures that may be interpreted in terms of the depositional and the post-depositional history of the deposits. Inclusions of sulfides or other minerals reveal information on the timing of the crystallization or recrystallization of the pyrite; chemical mapping of elements such as Ni, Co, and As reveals information on the relative time of transport of these elements in the ore fluids. Received: 19 March 1997 / Accepted: 14 May 1998  相似文献   

A submarine channel between the deepest parts of the Arkona and the Bornholm basins in the Baltic Sea     

Dr. Birger Larsen  Dr. Friedrich-C. Kögler 《Ocean Dynamics》1975,28(6):274-276

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Shear and tension hydraulic fractures in low permeability rocks     

P. Solberg  D. Lockner  J. Byerlee 《Pure and Applied Geophysics》1977,115(1-2):191-198

Laboratory hydrofracture experiments were performed on triaxially stressed specimens of oil shale and low-permeability granite. The results show that either shear or tension fractures could develop depending on the level of differentials stress, even in specimens containing preexisting fractures. With 1 kb of confining pressure and differential stress greater than 2kb, hydraulic fluid diffusion into the specimens reduced the effective confining pressure until failure occurred by shear fracture. Below 2kb of differential stress, tension fractures occurred. These results suggest that hydraulic fracturing in regions of significant tectonic stress may produce shear rather than tension fractures. In this casein situ stress determinations based on presumed tension fractures would lead to erroneous results.  相似文献