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101.
Alexander Jarosch Magnus T. Gudmundsson Thrdís Hgnadttir Gudni Axelsson 《Journal of Volcanology and Geothermal Research》2008,170(3-4):218-229
In the subglacial eruption at Gjálp in October 1996 a 6 km long and 500 m high subglacial hyaloclastite ridge was formed while large volumes of ice were melted by extremely fast heat transfer from magma to ice. Repeated surveying of ice surface geometry, measurement of inflow of ice, and a full Stokes 2-D ice flow model have been combined to estimate the heat output from Gjálp for the period 1996–2005. The very high heat output of order 106 MW during the eruption was followed by rapid decline, dropping to 2500 MW by mid 1997. It remained similar until mid 1999 but declined to 700 MW in 1999–2001. Since 2001 heat output has been insignificant, probably of order 10 MW. The total heat carried with the 1.2 × 1012 kg of basaltic andesite erupted (0.45 km3 DRE) is estimated to have been 1.5 × 1018 J. About two thirds of the thermal energy released from the 0.7 km3 edifice in Gjálp occurred during the 13-day long eruption, 20% was released from end of eruption until mid 1997, a further 10% in 1997–2001, and from mid 2001 to present, only a small fraction remained. The post-eruption heat output history can be reconciled with the gradual release of 5 × 1017 J thermal energy remaining in the Gjálp ridge after the eruption, assuming single phase liquid convection in the cooling edifice. The average temperature of the edifice is found to have been approximately 240 °C at the end of the eruption, dropping to 110 °C after 9 months and reaching 40 °C in 2001. Although an initial period of several months of very high permeability is possible, the most probable value of the permeability from 1997 onwards is of order 10− 12 m2. This is consistent with consolidated/palagonitized hyaloclastite but incompatible with unconsolidated tephra. This may indicate that palagonitization had advanced sufficiently in the first 1–2 years to form a consolidated hyaloclastite ridge, resistant to erosion. No ice flow traversing the Gjálp ridge has been observed, suggesting that it has effectively been shielded from glacial erosion in its first 10 years of existence. 相似文献
102.
Chemical Weathering Rates, Erosion Rates and Mobility of Major and Trace Elements in a Boreal Granitic Till 总被引:1,自引:0,他引:1
Chemical weathering rates and erosionrates of granitic till in northern Sweden have beenestimated. The present-day chemical weathering rate iscompared with the long-term average weathering ratesince the last deglaciation approximately 8,700 yearsago. Also, the present-day release rates of major andtrace elements due to chemical weathering are comparedwith the mobility of these elements in a spodosolprofile as shown by soil water samples from the vadozezone. The estimation of the past weathering rate isbased on elemental depletion trends in a soil profile(typic haplocryod), whereas the present weatheringrate is based on elemental input/output budgets in asmall catchment (9.4 km2). The long-term averagechemical erosion rate, expressed as the sum of majorelement oxides (SiO2, Al2O3, CaO,Fe2O3, K2O, MgO, MnO, Na2O,P2O5, TiO2), was estimated to be4.9 gm-2 yr-1. The long-term base cation(Ca2+, Mg2+, Na+, K+) depletionwas 0.325 keq ha-1 yr-1. The currentchemical erosion rate was estimated to be2.43.0 g -2 yr-1, which is at least an order ofmagnitude higher than the rate of physical erosion,and the base cation flux due to chemical weathering is0.356–0.553~keq ha-1 yr-1. However,0.074 keq ha-1 yr-1 of this flux may be related tocation exchange processes induced by atmospheric inputof acid rain. There is no evidence for any recentlyincreased weathering rate of silicates in this area.The inputs of Cd, Cu, Ni and Zn exceed the outputs,and hence, these elements are currently accumulatingin the soil.There is a distinct seasonal variation in thechemical composition of the soil water. Results fromthe soil water samples show that Na, followed by Siand S (Cl was not measured), are the most mobileelements in the spodosol profile between the E-horizonand the C-horizon, and that Al and Fe were the leastmobile elements. However, there is no simplerelationship between the mobility of an element in thespodosol profile and the current release rate due toweathering of that element. This fact may haveimplications for the validity of the comparisonbetween the past and present weathering rates asperformed in this study. 相似文献
103.
The last ice sheet over the British Isles, together with other mid-latitude Pleistocene ice sheets, and in contrast to the modern ice sheets of Greenland and Antarctica, had a relatively low profile, low summit elevation and extensive, elongated lobes at its margin. A thermo-mechanically coupled numerical ice sheet model, driven by a proxy climate, has been used to explore the properties that would have permitted these characteristics to develop. The approach, the key to quantitative palaeoglaciology, is to determine the boundary conditions that permit the simulated ice sheet to mimic the evolution of the real ice sheet through the last glacial cycle. Simulations show how a British ice sheet may have been confluent with a Scandinavian ice sheet during some parts of its history and how unforced periodic and asynchronous oscillations could occur in different parts of its margins. Marginal lobes are a reflection of streaming within the ice sheet. Such streams can be ephemeral, dynamic streams located because of ice sheet properties, or fixed streams whose location is determined by bed properties. The simulations that best satisfy constraints of extent, elevation and relative sea levels are those with major fixed streams that strongly draw down the ice sheet surface. In these, the core upland areas of the ice sheet were cold based at the Last Glacial Maximum, basal streaming velocities were between 500 and 1000 ma−1 compared with surface velocities of 10–50 ma−1 in inter-stream zones, shear stresses were as low as 15–25 kPa in streams compared with 70–110 kPa in upland areas and 60–84% of the ice flux was delivered to the margin via streams. 相似文献
104.
105.
106.
Magnus Karlsson Colin Craven Patricia M. Dove William H. Casey 《Aquatic Geochemistry》2001,7(1):13-32
The empirical rate laws formulated to describe the dissolution rates of oxide minerals include the surface charge concentration that results from the protonation and deprotonation of surface functional groups. Previous experiments on quartz and silica have shown that dissolution rates vary as a function of different background electrolyte solutions, however, such experiments are often conducted at elevated temperatures where it is difficult to estimate surface charge along with the dissolution rates. In the present study we measuresurface charge concentrations for silica in different electrolyte solutions at 298 K in order to quantify the extent to which the different counterions could affect the dissolution rates through their influence on the surface charge concentrations. The experimental solutions in the electrolyte series: LiCl, NaCl, KCl, RbCl, CaCl2, SrCl2 and BaCl2 were prepared to maintain a constant metal concentration of 1.0 M. For the alkali-metal chlorides, the surface charge concentrations correlate with the size of the hydrated alkali metal, consistent with the idea that these counterions affect charge via outer-sphere coordination that shield proton surface complexes from one another. The reactivity trend for alkaline-earth cations is less clear, but the data demonstrate distinct differences in the acid-base propertiesof the silica surface in these different electrolytes. We then discuss how these trends are manifested in the rate equations used to interpret dissolution experiments. 相似文献