Climatic forcing before,during, and after the 8.2 Kyr B.P. global cooling event     

Devendra Lal  William G. Large  Stephan G. Walker 《Journal of Earth System Science》2007,116(3):171-177

This paper attempts at full characterization of the unique global 8.2 Kyr B.P. cooling event. Significant atmospheric cooling started during 9.5–8.5 Kyr B.P. when the Sun was extremely quiet during three periods of ∼ 50–100 years. The flood of melt water in the N. Atlantic from glacial lakes during the demise of the Laurentide ice sheet, starting at ∼ 8.5 Kyr B.P., adds to the atmospheric cooling. Climatic forcing events occurred at 8.5 Kyr B.P., at 8.2 Kyr B.P. and finally at 8.06 Kyr B.P., leading to concurrent increases or decreases in the atmospheric Δ¹⁴C levels, completely consistent with the climatic forcing proposed here.  相似文献   

Field experiments yield new insights into gas exchange and excess air formation in natural porous media     

Stephan Klump  Yama Tomonaga  Wolfgang Kinzelbach  Dieter M. Imboden 《Geochimica et cosmochimica acta》2007,71(6):1385-1397

Gas exchange between seepage water and soil air within the unsaturated and quasi-saturated zones is fundamentally different from gas exchange between water and gas across a free boundary layer, e.g., in lakes or rivers. In addition to the atmospheric equilibrium fraction, most groundwater samples contain an excess of dissolved atmospheric gases which is called “excess air”. Excess air in groundwater is not only of crucial importance for the interpretation of gaseous environmental tracer data, but also for other aspects of groundwater hydrology, e.g., for oxygen availability in bio-remediation and in connection with changes in transport dynamics caused by the presence of entrapped air bubbles. Whereas atmospheric solubility equilibrium is controlled mainly by local soil temperature, the excess air component is characterized by the (hydrostatic) pressure acting on entrapped air bubbles within the quasi-saturated zone. Here we present the results of preliminary field experiments in which we investigated gas exchange and excess air formation in natural porous media. The experimental data suggest that the formation of excess air depends significantly on soil properties and on infiltration mechanisms. Excess air was produced by the partial dissolution of entrapped air bubbles during a sprinkling experiment in fine-grained sediments, whereas similar experiments conducted in coarse sand and gravel did not lead to the formation of excess air in the infiltrating water. Furthermore, the experiments revealed that the noble gas temperatures determined from noble gases dissolved in seepage water at different depths are identical to the corresponding in situ soil temperatures. This finding is important for all applications of noble gases as a paleotemperature indicator in groundwater since these applications are always based on the assumption that the noble gas temperature is identical to the (past) soil temperature.  相似文献   

David Henry Keen (1947-2006)     

Stephan Harrison 《Proceedings of the Geologists' Association. Geologists' Association》2007,118(2):213-216

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Laboratory studies about the interaction of ammonia with ice crystals at temperatures between 0 and −20°C     

Ines Hoog  Subir K. Mitra  Karoline Diehl  Stephan Borrmann 《Journal of Atmospheric Chemistry》2007,57(1):73-84

In laboratory experiments the interactions of ammonia with ice crystals were studied within the temperature range between 0 and −20°C. In a first series of experiments dendritic ice crystals were grown from water vapor in presence of ammonia gas in various concentrations between 4 and 400 ppbv. In a second series of experiments pure ice crystals were exposed to a humidified ammonia–air mixture inside a horizontal flow tube. The influence of temperature, ammonia gas concentration (0.6, 1.5, and 10 ppmv), exposure time, and the presence of impurities such as sulfate on the ammonia uptake by the ice surface was investigated by determining the ammonium content in the melt water of the ice crystals by ion chromatography. During the growth of ice crystals significant amounts of ammonia (around 200 μg/l) were taken up even at small gas concentrations. In contrast, even at high gas concentrations the uptake of ammonia by non-growing ice crystals was lower by approximately one order of magnitude. The presence of sulfate on the ice surface affected an enhanced uptake of ammonia by a factor of 5–10. A model is presented which describes the uptake of ammonia by ice considering the chemical processes occurring in the ice surface layer and simultaneous diffusion of ammonia into bulk ice. Even the increased uptake of ammonia by growing ice is rather small compared to the uptake by water droplets; thus, the major process for scavenging of ammonia from the atmosphere via the ice phase might not be the direct uptake by ice crystals but the riming involving super-cooled droplets containing ammonia.  相似文献   

Trace element partitioning between apatite and silicate melts   总被引：7，自引：0，他引：7  

Stefan Prowatke  Stephan Klemme 《Geochimica et cosmochimica acta》2006,70(17):4513-4527

We present new experimental apatite/melt trace element partition coefficients for a large number of trace elements (Cs, Rb, Ba, La, Ce, Pr, Sm, Gd, Lu, Y, Sr, Zr, Hf, Nb, Ta, U, Pb, and Th). The experiments were conducted at pressures of 1.0 GPa and temperatures of 1250 °C. The rare earth elements (La, Ce, Pr, Sm, Gd, and Lu), Y, and Sr are compatible in apatite, whereas the larger lithophile elements (Cs, Rb, and Ba) are strongly incompatible. Other trace elements such as U, Th, and Pb have partition coefficients close to unity. In all experiments we found D_Hf > D_Zr, D_Ta ≈ D_Nb, and D_Ba > D_Rb > D_Cs. The experiments reveal a strong influence of melt composition on REE partition coefficients. With increasing polymerisation of the melt, apatite/melt partition coefficients for the rare earth elements increase for about an order of magnitude. We also present some results in fluorine-rich and water-rich systems, respectively, but no significant influence of either H₂O or F on the partitioning was found. Furthermore, we also present experimentally determined partition coefficients in close-to natural compositions which should be directly applicable to magmatic processes.  相似文献   

Timing of Uralian orogenic gold mineralization at Kochkar in the evolution of the East Uralian granite-gneiss terrane     

Jochen Kolb  Sven Sindern  Alexander F. M. Kisters  F. Michael Meyer  Stephan Hoernes  Jens Schneider 《Mineralium Deposita》2005,40(5):473-491

Gold mineralization at Kochkar (Urals, Russia) is hosted mainly by quartz lodes, which developed at lithological contacts between mafic dikes and granitoids of the Plast massif during late Carboniferous to early Permian, regional E–W compression in the East Uralian Zone (EUZ). The alteration mineralogy in mafic dikes comprises biotite, actinolite, albite, K-feldspar, quartz, epidote, tourmaline, sericite, pyrite, arsenopyrite, chalcopyrite, sphalerite, fahlores, galena, bismuthinite, and gold, and in Plast granitoids quartz, sericite, calcite, epidote, and ore minerals. Geochemically, an enrichment of Si, K, Rb, Ba, S, base metals, W, and Au can be observed. The ore fluid had δ¹⁸O values between 8.2‰ and 9.5‰ typical for metamorphic or deep magmatic fluids. The tectonometamorphic evolution of the EUZ is marked by peak metamorphic conditions at 635±40°C and 5–6 kbar through 500±20°C during gold mineralization, and 300–350°C and 2–3 kbar. The last event was dated on a late, barren quartz vein formed during greenschist facies metamorphism at 265±3 Ma by the Rb–Sr method. Fluids related to this overprint had a δ¹⁸O value of 5.2‰ and an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70685 indicating that they are largely equilibrated with metamorphic lithologies of the EUZ. The Plast granitoids and the adjacent Borisov granite, which was dated at 358±23 Ma (U–Pb zircon age), have an adakitic character. This, together with the arc-signature of the mafic dikes, supports the setting of the EUZ within the Valerianovsky continental arc. Eastward subduction of the Uralian Ocean below this arc began during the late Devonian to early Carboniferous. Between 320 and 265 Ma, the oblique closure of the ocean resulted in doming of granitoid massifs in a sinistral transpressional regime, subsequent retrograde gold mineralization during E–W compression and a later greenschist facies overprint. This long-lasting retrograde evolution of the EUZ was caused by the lack of postcollisional collapse. Heat for a “deep-later" type of metamorphism and triggering the auriferous fluid system was supplied by radiogenic heating of an overthickened crust. The greenschist facies overprint at Kochkar and coeval crustal melting in the EUZ was additionally initiated by local external heating of the terrane. This could have been caused by syn- to postcollisional slab rollback or delamination resulting in magmatic underplating of the EUZ, which postdates orogenic gold mineralization at Kochkar. The tectonic interpretation of the EUZ indicates that gold mineralization at Kochkar formed in a mid-crustal environment of a continental magmatic arc at the cessation of active subduction predating post orogenic plutonism.  相似文献   

The effect of Cr on the solubility of Al in orthopyroxene: experiments and thermodynamic modelling   总被引：1，自引：1，他引：0  

Stephan Klemme  Hugh StC O'Neill 《Contributions to Mineralogy and Petrology》2000,138(1):84-98

The partitioning of chromium and aluminium between coexisting orthopyroxene and spinel in equilibrium with forsterite in the system MgO–Al₂O₃–SiO₂–Cr₂O₃ (MAS–Cr) has been experimentally determined as a function of temperature, pressure and Cr/(Cr + Al) ratio. Experiments were conducted at temperatures between 1300 and 1500 °C and at pressures from 5 to 54 kbar. Previous experimental results on the (Al, Cr)₂O₃ and Mg(Al, Cr)₂O₄ solid solutions have been combined with the present results plus relevant data from the CMAS system to derive a thermodynamic model for Al–Cr-bearing orthopyroxenes, spinels and corundum–eskolaite solid solutions. The orthopyroxene solid solution can be modelled within the accuracy of all experimental constraints as a ternary solid solution involving the components Mg₂Si₂O₆ ( E), MgAl₂SiO₆ (M) and MgCr₂SiO₆ (C), in which the activities are related to composition through the equations: The mole fractions are defined as where n _Al and n _Cr are the number of Al and Cr cations per orthopyroxene formula unit of six oxygens. These expressions reduce to one-site mixing for Mg₂Si₂O₆–MgAl₂SiO₆ orthopyroxenes in the Cr-free system, but are equivalent to two-site mixing for the exchange of Al and Cr between orthopyroxene and spinel, as required by the experimental data. We find W ^opx _EM =W ^opx _EC  = 20 kJ mol⁻¹ and W ^opx _MC =0. Received: 9 August 1999 / Accepted: 18 February 2000  相似文献   

The near-solidus transition from garnet lherzolite to spinel lherzolite   总被引：20，自引：1，他引：19  

Stephan Klemme  Hugh StC. O'Neill 《Contributions to Mineralogy and Petrology》2000,138(3):237-248

The position of the transition from spinel lherzolite to garnet lherzolite in the system CaO-MgO-Al₂O₃-SiO₂ (CMAS) has been determined experimentally at near-solidus temperatures. In reversed experiments, the transition occurs between 18 and 20 kbar at 1200 °C and between 26 and 27 kbar at 1500 °C, corresponding to higher pressures than previously envisaged. A position for the transition deeper within the Earth further complicates the explanation of the so-called garnet signatures in the trace element and isotope patterns of mid-ocean ridge basalts. If melting during adiabatic upwelling beneath a mid-ocean ridge begins at the depth required for the stability of garnet in peridotitic compositions, simple melting models predict that the amount of melt produced should be much greater than the observed thickness of the oceanic crust. A partial solution to the apparent conflict might be that (1) the rather simplistic melting models are in error, (2) that melting begins in garnet pyroxenite veins that are believed to be stable at lower pressures than garnet lherzolite or (3) that melting does not involve garnet at all, but it is clinopyroxene causing the trace element patterns observed in basalts erupted at mid-ocean ridges. A second set of reversal experiments were conducted to investigate the solubility of alumina in both orthopyroxenes and clinopyroxenes at the high temperatures near the solidus in the system CMAS. The results are compatible with most previous studies, and may be used as a starting point to calibrate thermodynamic models for pyroxenes in chemical systems, approximating upper mantle chemistry. Received: 9 August 1999 / Accepted: 29 October 1999  相似文献   

The offshore east African rift system: new insights from the Sakalaves seamounts (Davie Ridge,SW Indian Ocean)          下载免费PDF全文

Simon Courgeon  Patrick Bachèlery  Gwénael Jouet  Stephan J. Jorry  Esther Bou  Marcelle K. BouDagher‐Fadel  Sidonie Révillon  Gilbert Camoin  Emmanuelle Poli 《地学学报》2018,30(5):380-388

The offshore branch of the East African Rift System (EARS) has developed during Late Cenozoic time along the eastern Africa continental margin. While Neogene–Pleistocene extensional tectonic deformation has been evidenced along the northern segment of the Davie Ridge, the spatial extent of deformation further south remains poorly documented. Based on recent and various oceanographic datasets (bathymetric surveys, dredge samples and seismic profiles), our study highlights active normal faulting, modern east–west extensional tectonic deformation and Late Cenozoic alkaline volcanism at the Sakalaves Seamounts (18°S, Davie Ridge) that seem tightly linked to the offshore EARS development. In parallel, rift‐related tectonic subsidence appears responsible for the drowning of the Sakalaves Miocene shallow‐water carbonate platform. Our findings bring new insights regarding the development of the EARS offshore branch and support recent kinematic models proposing the existence of a plate boundary across the Mozambique Channel.  相似文献   

Late Pleistocene Eifel eruptions: insights from clinopyroxene and glass geochemistry of tephra layers from Eifel Laminated Sediment Archive sediment cores     

Michael W. Förster  Anastasia Zemlitskaya  Laura M. Otter  Stephan Buhre  Frank Sirocko 《第四纪科学杂志》2020,35(1-2):186-198

The Eifel Laminated Sediment Archive (ELSA), which comprises several cores from maar lakes, includes numerous tephra layers spanning the last 140 000 years. The sediment cores are dated by ¹⁴C and thermoluminescence as well as tuned to Greenland stadial–interstadial successions. Within the last glacial cycle, the Eifel Volcanic Fields are source to several widespread tephra layers, namely the Laacher See, Eltville, Rambach and Rocourt Tephra. However, a corresponding source volcano was so far only identified for the Laacher See Tephra. In this study we use glass and clinopyroxene geochemistry to link the remaining tephra layers to possible eruption centers within the West and East Eifel Volcanic Fields: while we demonstrate that the Eltville Tephra originated from an earlier eruption of the Laacher See Volcano at 24 300 a bp from within the East Eifel Volcanic Field, the Rambach and Rocourt Tephras are sourced from the West Eifel Volcanic Field and erupted from Wartgesberg at 27 900 a bp and Pulvermaar at 75 000 a bp , respectively. Phases of volcanic activity peaked at 10 000–30 000 and 60 000–80 000 a bp and were thus erupted around the temperature minima of the last glacial cycle. The longest phase of dormancy between individual vents was around 30 000 years long, within the last interglacial.  相似文献