Deglacial land emergence and lateral upper-mantle heterogeneity in the Svalbard Archipelago—II. Extended results for high-resolution load models     

Georg Kaufmann  Detlef Wolf 《Geophysical Journal International》1996,127(1):125-140

In Paper I (Breuer & Wolf 1995), a preliminary interpretation of the postglacial land emergence observed at a restricted set of six locations in the Svalbard Archipelago was given. The study was based on a simple model of the Barents Sea ice sheet and suggested increases in lithosphere thickness and asthenosphere viscosity with increasing distance from the continental margin.
In the present paper, the newly developed high-resolution load model. BARENTS-2, and land-uplift observations from an extended set of 25 locations are used to study further the possibility of resolving lateral heterogeneity in the upper mantle below the northern Barents Sea. A comparison of the calculated and observed uplift values shows that the lithosphere thickness is not well resolved by the observations, although values above 110 km are most common for this parameter. In contrast to this, there are indications of a lateral variation of asthenosphere viscosity. Whereas values in the range 10¹⁸-10²⁰Pas are inferred for locations close to the continental margin, 10²⁰-10²¹ Pa s are suggested further away from the margin.
A study of the sensitivity of the values found for lithosphere thickness and asthenosphere viscosity to modifications of load model BARENTS-2 shows that such modifications can be largely accommodated by appropriate changes in lithosphere thickness, whereas the suggested lateral variation of asthenosphere viscosity is essentially unaffected. An estimate of the influence of the Fennoscandian. ice sheet leads to the conclusion that its neglect results in an underestimation of the thickness of the Barents Sea ice sheet by about 10 per cent.  相似文献   

Note on estimates of the glacial-isostatic decay spectrum for Fennoscandia     

Detlef Wolf 《Geophysical Journal International》1996,127(3):801-805

For more than 30 years, Sauramo's (1958) shoreline diagram of the Fennoscandian uplift has been used in geophysical studies for estimates of the glacial-isostatic decay spectrum in order to infer from it the viscosity stratification in the Earth's mantle below Fennoscandia. The intent of the present note is to point out that more recent geological studies suggest that Sauramo's shoreline diagram is an incorrect representation of the Fennoscandian uplift. Geophysical interpretations based on the diagram may therefore require revision.  相似文献   

International geopolitical research colloquium on Euro-Atlantic security — a fresh start     

K. -A. Boesler  Detlef Herold  C. George 《GeoJournal》1995,37(2):286-286

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Experimentelle Untersuchung der Metamorphose von kieselig dolomitischen Sedimenten     

Paul Metz  Detlef Puhan 《Contributions to Mineralogy and Petrology》1970,26(4):302-314

During an experimental investigation of the metamorphism of siliceous dolomites the equilibrium data of the heterogeneous bivariant reaction 1 $$3{\text{ dolomite + 4 quartz + 1 H}}_{\text{2}} O \rightleftharpoons + 3 calcite + 3 CO_2 $$ were determined for the total fluid pressures of 1,000, 3,000 and 5,000 bars. The equilibrium conditions were found by experiments in which dolomite, quartz and water react to form talc, calcite and CO₂, as well as by experiments with reversible reaction direction. Results are shown on the temperature- \(X_{CO_2 } \) -diagram of Fig. 3. The temperature of formation of talc and calcite depends to a considerable extent on the composition of the CO₂-H₂O-gas phase; this can be read straight off the isobaric (P _f =const.) equilibrium curves in Fig. 3. In addition a strong dependence of the equilibrium temperature on the total pressure P _f was established (see Fig. 5). At a total gas pressure of 1,000 bars dolomite and quartz can react, according to the composition of the CO₂-H₂O-gas phase, to talc and calcite over the whole of the temperature range between about 350° and 490° C. This indicates that at low pressures the formation of talc and calcite takes place in the field of the albite-epidote-hornfels facies. At a pressure of 3,000 bars dolomite and quartz are stable up to about 550° C if the fluid phase is rich in carbon dioxide and correspondingly poor in water. Thus, this paragenesis can occur up to the stability field of staurolite [see annotation (5)] if the partial pressure of CO₂ is large. At the higher total gas pressure of 5,000 bars dolomite and quartz react even at medium CO₂-concentrations only at about 580° C to give talc and calcite. Therefore it is expected that in regional metamorphism at about 5,000 bars pressure or more the paragenesis dolomite plus quartz exists up to and within the stability field of staurolite and reacts only here to form talc and calcite after reaction (1) or tremolite and calcite after the following reaction (2)¹: $$5 dolomite + 8 quartz + 1 H_2 O \rightleftharpoons 1 tremolite + 3 calcite + 7 CO_2 $$ . The exact physico-chemical conditions under which dolomite, quartz and water react on the one hand to form talc, calcite and CO₂, and on the other hand to form tremolite, calcite and carbon dioxide, will be discussed later when our experimental investigations on the formation of tremolite are completed. First results were already published in a short note by Metz, Puhan and Winkler (1968).  相似文献   

Thallium isotope composition of the upper continental crust and rivers—An investigation of the continental sources of dissolved marine thallium     

Sune G. Nielsen  Mark Rehkämper  Per Andersson  Peter W. Swarzenski  Detlef Günther 《Geochimica et cosmochimica acta》2005,69(8):2007-2019

The thallium (Tl) concentrations and isotope compositions of various river and estuarine waters, suspended riverine particulates and loess have been determined. These data are used to evaluate whether weathering reactions are associated with significant Tl isotope fractionation and to estimate the average Tl isotope composition of the upper continental crust as well as the mean Tl concentration and isotope composition of river water. Such parameters provide key constraints on the dissolved Tl fluxes to the oceans from rivers and mineral aerosols.The Tl isotope data for loess and suspended riverine detritus are relatively uniform with a mean of ε²⁰⁵Tl = −2.0 ± 0.3 (ε²⁰⁵Tl represents the deviation of the ²⁰⁵Tl/²⁰³Tl isotope ratio of a sample from NIST SRM 997 Tl in parts per 10⁴). For waters from four major and eight smaller rivers, the majority were found to have Tl concentrations between 1 and 7 ng/kg. Most have Tl isotope compositions very similar (within ±1.5 ε²⁰⁵Tl) to that deduced for the upper continental crust, which indicates that no significant Tl isotope fractionation occurs during weathering. Based on these results, it is estimated that rivers have a mean natural Tl concentration and isotope composition of 6 ± 4 ng/kg and ε²⁰⁵Tl = −2.5 ± 1.0, respectively.In the Amazon estuary, both additions and losses of Tl were observed, and these correlate with variations in Fe and Mn contents. The changes in Tl concentrations have much lower amplitudes, however, and are not associated with significant Tl isotope effects. In the Kalix estuary, the Tl concentrations and isotope compositions can be explained by two-component mixing between river water and a high-salinity end member that is enriched in Tl relative to seawater. These results indicate that Tl can display variable behavior in estuarine systems but large additions and losses of Tl were not observed in the present study.  相似文献   

Tellurium isotopic composition of the early solar system—A search for effects resulting from stellar nucleosynthesis, Sn decay, and mass-independent fractionation     

Manuela A. Fehr  Mark Rehkämper  Alex N. Halliday  Uwe Wiechert  Detlef Günther  Jennifer L. Eigenbrode  Douglas Rumble III 《Geochimica et cosmochimica acta》2005,69(21):5099-5112

New precise Te isotope data acquired by multiple collector inductively coupled plasma mass spectrometry (MC-ICPMS) are presented for selected extraterrestrial and terrestrial materials. Bulk samples of carbonaceous, ordinary and enstatite chondrites as well as the metal and sulfide phases of iron meteorites were analyzed to search for nucleosynthetic isotope anomalies and to find evidence of formerly live ¹²⁶Sn, which decays to ¹²⁶Te with a half-life of 234,500 yr. None of the meteorites show evidence of mass dependent Te isotope fractionations larger than 2‰ for δ^126/128Te. Following internal normalization of the data to ¹²⁵Te/¹²⁸Te, the Te isotope ratios of all analyzed meteorites were found to be identical to a terrestrial standard, within uncertainties. This provides evidence that the regions of the solar disk that were sampled during accretion of the meteorite parent bodies were well mixed and homogeneous on a large scale, with respect to Te isotopes. The data acquired for bulk carbonaceous chondrites indicate that the initial ¹²⁶Sn/¹¹⁸Sn ratio of the solar system was <4 × 10⁻⁵, but this is dependent on the assumption that no redistribution of Sn and Te occurred since the start of the solar system. Five Archean sedimentary sulfides that display both mass dependent and mass-independent isotope effects for S yield internally normalized Te isotope data, which indicate that mass-independent Te isotope effects are absent. The mass dependent fractionations in these samples are constrained to be less than ∼1‰ for δ^126/128Te.  相似文献   

Magnetic anisotropy of calcite at room-temperature     

Volkmar Schmidt  Detlef Günther  Ann M. Hirt 《Tectonophysics》2006,418(1-2):63

The intrinsic room temperature magnetic properties of pure calcite were determined from a series of natural crystals, and they were found to be highly dependent on the chemical composition. In general, dia-, para-, and ferromagnetic components contribute to the magnetic susceptibility and the anisotropy of magnetic susceptibility (AMS). With a combination of magnetic measurements and chemical analysis these three contributions were determined and related to their mineralogical sources. The intrinsic diamagnetic susceptibility of pure calcite is − 4.46 ± 0.16 × 10^− 9 m³/kg (− 12.09 ± 0.5 × 10^− 6 SI) and the susceptibility difference is 4.06 ± 0.03 × 10^− 10 m³/kg (1.10 ± 0.01 × 10^− 6 SI). These diamagnetic properties are easily dominated by other components. The paramagnetic contribution is due to paramagnetic ions in the crystal lattice that substitute for calcium; these are mainly iron and manganese. The measured paramagnetic susceptibility agrees with the values calculated from the known concentration of paramagnetic ions in the crystals according to the Curie law of paramagnetic susceptibility. Substituted iron leads to an increase in the AMS. The paramagnetic susceptibility difference was found to correlate linearly with the iron content for concentrations between 500 and 10,000 ppm. An empirical relation was determined: (k₁ − k₃)^para (kg/m³) = Fe-content (ppm) × (1 ± 0.1) × 10^− 12 (kg/m³/ppm). The maximum susceptibility difference (Δk = k₁ − k₃) was found to be unaffected by iron contents below 100 ppm. Ferromagnetic contributions due to inclusions of ferromagnetic minerals can dominate the susceptibility. They were detected by acquisition of isothermal remanent magnetization (IRM) and their contribution to the AMS was separated by high-field measurements.  相似文献   

Multi-gas Emissions Pathways to Meet Climate Targets   总被引：1，自引：1，他引：1  

Malte Meinshausen  Bill Hare  Tom M. M. Wigley  Detlef Van Vuuren  Michel G. J. Den Elzen  Rob Swart 《Climatic change》2006,75(1-2):151-194

So far, climate change mitigation pathways focus mostly on CO₂ and a limited number of climate targets. Comprehensive studies of emission implications have been hindered by the absence of a flexible method to generate multi-gas emissions pathways, user-definable in shape and the climate target. The presented method ‘Equal Quantile Walk’ (EQW) is intended to fill this gap, building upon and complementing existing multi-gas emission scenarios. The EQW method generates new mitigation pathways by ‘walking along equal quantile paths’ of the emission distributions derived from existing multi-gas IPCC baseline and stabilization scenarios. Considered emissions include those of CO₂ and all other major radiative forcing agents (greenhouse gases, ozone precursors and sulphur aerosols). Sample EQW pathways are derived for stabilization at 350 ppm to 750 ppm CO₂ concentrations and compared to WRE profiles. Furthermore, the ability of the method to analyze emission implications in a probabilistic multi-gas framework is demonstrated. The probability of overshooting a 2 ^∘C climate target is derived by using different sets of EQW radiative forcing peaking pathways. If the probability shall not be increased above 30%, it seems necessary to peak CO₂ equivalence concentrations around 475 ppm and return to lower levels after peaking (below 400 ppm). EQW emissions pathways can be applied in studies relating to Article 2 of the UNFCCC, for the analysis of climate impacts, adaptation and emission control implications associated with certain climate targets. See for EQW-software and data.  相似文献   

Compressible viscoelasticity: stability of solutions for homogeneous plane-Earth models     

Volker Klemann  Patrick Wu  Detlef Wolf 《Geophysical Journal International》2003,153(3):569-585

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Sodic Pyroxene and Sodic Amphibole as Potential Reference Materials for In Situ Lithium Isotope Determinations by SIMS     

Michael A.W. Marks  Roberta L. Rudnick  Thomas Ludwig  Horst Marschall  Thomas Zack  Ralf Halama  William F. McDonough  Detlef Rost  Thomas Wenzel  Edward P. Vicenzi  Ivan P. Savov  Rainer Altherr  Gregor Markl 《Geostandards and Geoanalytical Research》2008,32(3):295-310

Two large pegmatitic crystals of sodic pyroxene (aegirine) and sodic amphibole (arfvedsonite) from the agpaitic igneous Ilímaussaq Complex, south Greenland were found to be suitable as reference materials for in situ Li isotope determinations. Lithium concentrations determined by SIMS and micro‐drilled material analysed by MC‐ICP‐MS generally agreed within analytical uncertainty. The arfvedsonite crystal was homogeneous with [Li] = 639 ± 51 μg g^?1 (2s, n = 69, MC‐ICP‐MS and SIMS results). The aegirine crystal shows strongly developed sector zoning, which is a common feature of aegirines. Using qualitative element mapping techniques (EPMA), the homogeneous core of the crystal was easily distinguished from the outermost sectors of the crystals. The core had a mean [Li] of 47.6 ± 3.6 μg g^?1 (2s, n = 33) as determined by SIMS. The seven micro‐drilled regions measured by solution MC‐ICP‐MS returned slightly lower concentrations (41–46 μg g^?1), but still overlap with the SIMS data within uncertainty. Based on MC‐ICP‐MS and SIMS analyses, the variation in δ⁷Li was about 1‰ in each of the two crystals, which is smaller than that in widely used glass reference materials, making these two samples suitable to serve as reference materials. There was, however, a significant offset between the results of MC‐ICP‐MS and SIMS. The latter deviated from the MC‐ICP‐MS results by ?6.0 ± 1.9‰ (2s) for the amphibole and by ?3.9 ± 1.9‰ (2s) for the aegirine. This indicates the presence of a significant matrix effect in SIMS determinations of Li isotopes for amphibole and pyroxene relative to the basalt glasses used for calibration. Based on the MC‐ICP‐MS results, mean δ⁷Li values of +0.7 ± 1.2‰ (2s, n = 10) for the arfvedsonite crystal and of ?3.7 ± 1.2‰ (2s, n = 7) for the core of the aegirine crystal were calculated. Adopting these values, SIMS users can correct for the specific IMF (instrumental mass fractionation) of the ion probe used. We propose that these two crystals serve as reference materials for in situ Li isotope determinations by SIMS and pieces of these two crystals are available from the first author upon request.  相似文献