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91.
The occurrence and distribution of polycyclic musks in the Lippe River system (a tributary of the Rhine River, Germany) was investigated in order to observe the dynamic transport and partitioning of these compounds between aqueous and particulate phases after their discharge into the river by sewage effluents. 1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta[g]-2-benzopyrane (HHCB), 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene (AHTN), 6-acetyl-1,1,2,3,3,5-hexamethylindane (AHMI) and 4-acetyl-1,1-dimethyl-6-tert.-butylindane (ADBI) concentrations were determined in 19 water and surface sediment samples which were taken from a longitudinal section of the river. HHCB and AHTN were present in each of the water samples at concentrations ranging from <10 to 180 ng l−1 and <10 to 70 ng l−1, respectively. The load of dissolved HHCB and AHTN was calculated on the basis of compound concentrations in water and the corresponding river runoff data and ranged from 3 to 293 g day−1 and from 1 to 108 g day−1, respectively. Increasing loads of HHCB and AHTN along the river reflect a high input of sewage effluents to the densely populated areas along the central part of the river. Decreasing loads at the lower reaches indicate that in the corresponding river sections the rate of removal of musks was higher than the rate of input. Degradation and/or adsorption to particulate matter are processes that might explain this phenomenon. Consequently, high concentrations of HHCB and AHTN were detected in surface sediments from the Lippe River (from 5 to 191 μg kg−1 and from 2 to 1399 μg kg−1, respectively). HHCB/AHTN ratios in sediment samples were lower (average 1.2) than in water samples (average 2.9), suggesting the preferential adsorption of AHTN to particulate matter.  相似文献   
92.
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   
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The kinetics of (Mg, Fe)SiO3 pyroxene layer growth within silicate thin films with total thickness <1 μm was studied experimentally at 0.1 MPa total pressure, controlled fO2 and temperatures from 1,000 to 1,300°C. The starting samples were produced by pulsed laser deposition. Layer thickness before and after the experiments and layer composition as well as microstructures, grain size and shape of the interfaces were determined by Rutherford back scattering and transmission electron microscopy assisted by focused ion beam milling. Due to the miniaturization of the starting samples and the use of high resolution analytical methods the experimentally accessible temperature range for rim growth experiments was extended by about 300°C towards lower temperatures. The thickness of the layers at a given temperature increases proprotional to the square root of time, indicating a diffusion-controlled growth mechanism. The temperature dependence of rim growth yields an apparent activation energy of 426 ± 34 kJ/mol. The small grain size in the orthopyroxene rims implies a significant contribution of grain boundary diffusion to the bulk diffusion properties of the polycrystalline rims. Based on microstructural observations diffusion scenarios are discussed for which the SiO2 component behaves immobile relative to the MgO component. Volume diffusion data for Mg in orthopyroxene from the literature indicate that the measured diffusivity is probably controlled by the mobility of oxygen. The observed reaction rates are consistent with earlier results from dry high-temperature experiments on orthopyroxene rim growth. Compared to high pressure experiments at 1,000°C and low water fugacities, reaction rates are 3–4 orders of magnitude smaller. This observation is taken as direct evidence for a strong effect of small amounts of water on diffusion in silicate polycrystals. In particular SiO2 changes from an immobile component at dry conditions to an extremely mobile component even at very low water fugacities.  相似文献   
96.
Ralf Greve 《Climatic change》2000,46(3):289-303
Numerical computations are performed with the three-dimensional polythermal ice-sheet model SICOPOLIS in order to investigate the possible impact of a greenhouse-gas-induced climate change on the Greenland ice sheet. The assumed increase of the mean annual air temperature above the ice covers a range from T = 1°C to 12°C, and several parameterizations for the snowfall and the surface melting are considered. The simulated shrinking of the ice sheet is a smooth function of the temperature rise, indications for the existence of critical thresholds of the climate input are not found. Within 1000 model years, the ice-volume decrease is limited to 10% of the present volume for T 3°C, whereas the most extreme scenario, T = 12°C, leads to an almost entire disintegration, which corresponds to a sea-level equivalent of 7 m. The different snowfall and melting parameterizations yield an uncertainty range of up to 20% of the present ice volume after 1000 model years.  相似文献   
97.
Investigation of sediment samples from Sites 1039 and 1040 (ODP Leg 170) drilled off the Nicoya peninsula (Costa Rica) by organic geochemical and organic petrological methods has revealed that subduction has only little influence on the composition of the sedimentary organic matter. Organic carbon contents reached 1.5% in the Pleistocene samples but Miocene and Pliocene sediments had an average organic carbon content of less than 0.5%. Organic carbon/sulfur ratios are generally below 2.8, reflecting an intense sulfate reduction in the uppermost sediments which was enhanced by sulfate supply both from sea water and deeper strata. Microscopical examinations indicate that the organic matter is mainly derived from marine sources. A small amount of terrigenous organic matter is, however, present as well according to n-alkane and fatty acid distributions. The alkenone unsaturation index U37k′ shows only a slight decrease during the Miocene and Pliocene, and stronger variations in the Pleistocene, probably indicating more stable sea surface temperatures during the Miocene and Pliocene. Variations in the Pleistocene can possibly be related to glacial/interglacial changes.  相似文献   
98.
The island of Salina comprises one of the most distinct calc-alkaline series of the Aeolian arc (Italy), in which calc-alkaline, high-K calc-alkaline, shoshonitic and leucite-shoshonitic magma series are developed. Detailed petrological, geochemical and isotopic (Sr, Nd, Pb, O) data are reported for a stratigraphically well-established sequence of lavas and pyroclastic rocks from the Middle Pleistocene volcanic cycle (430–127 ka) of Salina, which is characterized by an early period of basaltic volcanism (Corvo; Capo; Rivi; Fossa delle Felci, group 1) and a sequence of basaltic andesites, and andesites and dacites in the final stages of activity (Fossa delle Felci, groups 2–8). Major and trace element compositional trends, rare earth element (REE) abundances and mineralogy reveal the importance of crystal fractionation of plagioclase + clinopyroxene + olivine/ orthopyroxene ± titanomagnetite ± amphibole ± apatite in generating the more evolved magma types from parental basaltic magmas, and plagioclase accumulation in producing the high Al2O3 contents of some of the more evolved basalts. Sr isotope ratios range from 0.70410 to 0.70463 throughout the suite and show a well-defined negative correlation with 143Nd/144Nd (0.51275–0.51279). Pb isotope compositions are distinctly radiogenic with relatively large variations in 206Pb/204Pb (19.30–19.66), fairly constant 207Pb/204Pb (15.68–15.76) and minor variations in 208Pb/204Pb ratios (39.15–39.51). Whole-rock δ18O values range from +6.4 to +8.5‰ and correlate positively with Sr isotope ratios. Overall, the isotopic variations are correlated with the degree of differentiation of the rocks, indicating that only small degrees of crustal assimilation are overprinting the dominant evolution by crystal–liquid fractionation (AFC-type processes). The radiogenic and oxygen isotope composition of the Salina basalts suggests derivation from primary magmas from a depleted mantle source contaminated by slab-derived fluids and subducted sediments with an isotopic signature of typical upper continental crust. These magmas then evolved further to andesitic and dacitic compositions through the prevailing process of low-pressure fractional crystallization in a shallow magma reservoir, accompanied by minor assimilation of crustal lithologies similar to those of the Calabrian lower crust. Received: 29 November 1999 / Accepted: 16 April 2000  相似文献   
99.
An algorithm for the estimation of root zone soil moisture is presented. Global fields of the soil moisture within the uppermost metre of soil are derived with a temporal resolution of 10 days. For calibration, long-term soil moisture observations from the former Soviet Union are used. The variance of the measurements is largely dominated by the spatial variability of the long-term mean soil moisture, while the temporal variability gives comparatively small contribution. Consequently, the algorithm is organised into two steps. The first step concentrates on the retrieval of the spatial variance of the long-term means, which comprises more than 85% of the total soil moisture variability. A major part of the spatial variance can be explained by four easily available fields: the climatological precipitation, land use, soil texture, and terrain slope. The second step of the algorithm is dedicated to the local temporal variability. This part of variability is recovered by using passive microwave data from scanning multichannel microwave radiometre (SMMR) supported by monthly averaged fields of air temperature and precipitation. The 6-GHz channel of SMMR is shown to be severely disturbed by radio frequency interference, so that information from the 10-GHz channel is used instead. The algorithm provides reasonable soil moisture fields which is confirmed by a comparison with independent measurements from Illinois.  相似文献   
100.
Regional mean sea level changes in the German Bight are considered. Index time series derived from 15 tide gauge records are analysed. Two different methods for constructing the index time series are used. The first method uses arithmetic means based on all available data for each time step. The second method uses empirical orthogonal functions. Both methods produce rather similar results for the time period 1924–2008. For this period, we estimate that regional mean sea level increased at rates between 1.64 and 1.74 mm/year with a 90% confidence range of 0.28 mm/year in each case. Before 1924, only data from a few tide gauges are available with the longest record in Cuxhaven ranging back till 1843. Data from these tide gauges, in particular from Cuxhaven, thus receive increasingly more weight when earlier years are considered. It is therefore analysed to what extent data from Cuxhaven are representative for the regional sea level changes in the German Bight. While this cannot be clarified before 1924, it is found that this is not the case from 1924 onwards when changes in Cuxhaven can be compared to that derived from a larger data set. Furthermore, decadal variability was found to be substantial with relatively high values towards the end of the analysis period. However, these values are not unusual when compared to earlier periods.  相似文献   
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