Horwood, J.: The Sei Whale: Population Biology, Ecology & Management. Croom Helm Ltd. & Routledge, London, New York and Sidney     

Ulrike  Griehel 《Marine Ecology》1990,11(1):95-96

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Synthetic zeolites formed from expanded perlite: Type,formation conditions and properties     

Dr. Ulrike Barth-Wirsching  Dr. H. Höller  Dr. D. Klammer  Dr. B. Konrad 《Mineralogy and Petrology》1993,48(2-4):275-294

Summary The starting material used was expanded perlite with a grain size < 40 m (74.5 wt.% SiO₂; 12.5 wt.% Al₂O₃). This material is a waste product obtained during the production of expanded perlite. The experiments were carried out with KOH solutions, mixtures of KOH and NaOH solutions (1:1) as well as NaOH solutions in the concentration range 0.5 N to 6.0 N at temperatures of between 100° and 140°C and with reaction periods of 2 hours to 13 days in closed system. In the experiments with KOH containing solutions zeolite ZK-19 (phillipsite), W (merlinoite), G (chabazite) and F (edingtonite) formed. Without addition of aluminium high percentages of zeolite ZK-19 (80–100 wt.%) and zeolite W (90–100 wt.%) were obtained. The addition of aluminium rendered possibly the formation of 90 to 100 wt.% of zeolite G and 85 to 100 wt.% of zeolite F, respectively. In the experiments with NaOH solutions analcime, zeolite Na-Pc (gismondine), zeolite HS (sodalite hydrate) and zeolite A formed. High percentages of zeolite Na-Pc (90–100 wt.%), zeolite HS (up to 100 wt.%) and analcime (up to 100 wt.%) were synthesized without addition of aluminium. The formation of high percentages of zeolite A (95–100 wt.%), however, needs the addition of aluminium, NaCI and seed crystals. The temperature stability of the zeolites decreases in the following sequence: K-F > K-W K-ZK-19 (Na), K-W Na, K-F G_si-rich (Na), K-ZK-19 >> Na-Pc G_si-poor. Zeolite A has a very good temperature stability up to temperatures of } 550 °C similar to that of zeolite K-W. At higher temperatures, however, its stability is very poor. The NH₄ ⁺-exchange capacities (meq/g) of the different zeolites amount to the following values: ZK-19:2.8 - 3.2; W:3.0 - 3.2; G:2.3 - 3.6; A:3.1 - 3.2; Na-Pc:3.5 - 3.6; F : 3.9 - 4.8.

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Zeolithsynthese aus Blähperlit—Art, Bildungsbedingungen und Eigenschaften

Zusammenfassung Ausgangsmaterial der experimentellen Untersuchungen war Blähperlit mit einer Korngröße < 40 ,m (74,5 Gew.-% SiO₂; 12,5 Gew.-% Al₂O₃). Dieses Material ist ein Abfallprodukt, das bei der Produktion von Blähperlit anfällt. Die Experimente wurden mit KOH-Lösungen, Lösungsgemischen aus KOH und NaOH (1:1) sowie mit NaOH-Losungen im Konzentrationsbereich 0,5 n-6,0 n bei Temperaturen von 100° – 140°C und über Reaktionszeiten von 2 Stunden bis zu 13 Tagen im geschlossenen System durchgeführt. In den Experimenten mit KOH-hältigen Lösungen bildeten sich die Zeolithe ZK-19 (Phillipsit), W (Merlinoit), G (Chabasit) und F (Edingtonit). Hohe Prozentgehalte an Zeolith ZK-19 (80 – 100 Gew.-%) und Zeolith W (90–100 Gew.-%) entstehen nur ohne Zugabe von Aluminium. Die Bildung von 90–100 Gew.-% Zeolith G bzw. 85–100 Gew. % Zeolith F ist dagegen durch die Zugabe von Aluminium möglich. In den Experimenten mit NaOH-Lösungen bildeten sich die Zeolithe Analcim, Na-Pc (Gismondin), HS (Sodalithhydrat) und Zeolith A. Hohe Prozentanteile an Zeolith Na-Pc (90–100 Gew.-%), HS (bis zu 100 Gew. %) und Analcim (bis zu 100 Gew.-%) wurden ohne Aluminium-Zugabe synthetisiert. Die Bildung von hohen Gehalten an Zeolith A (95–100 Gew. %) ist jedoch nur unter Zugabe von Aluminium, NaCl und Kristallkeimen möglich.Die Temperaturbeständigkeit der Zeolithe nimmt in der folgenden Reihenfolge ab: K-F > K-W - K-ZK-19 (Na), K-W Na, K-F G_si-reich (Na), K-ZK-19 >> Na-Pc G_si-am. Zeolith A weist bis zu Temperaturen von etwa 550°C eine gute Temperaturbeständigkeit auf, die in etwa der von Zeolith K-W entspricht. Bei höheren Temperaturen ist die Beständigkeit jedoch sehr gering.Die NH⁴⁺-Austauschkapazitäten (mÄqu/g) der verschiedenen Zeolithe erreichen folgende Werte: ZK-19:2,8 - 3,2; W:3,0 - 3,2; G:2,3 - 3,6; A:3,1 - 3,2; Na-Pc:3,5 -3,6; F:3,9 - 4,8.

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Combining ordination techniques and geostatistics to determine the patterns of diatom distributions at Lake Lama, Central Siberia   总被引：4，自引：0，他引：4  

Ulrike Kienel  Thomas Kumke 《Journal of Paleolimnology》2002,28(2):181-194

The patterns of spatial variation of diatom assemblages from surface sediments in Lake Lama were quantified using a combined approach of ordination and geostatistics. The aims were (i) to estimate the amount of variation between diatom assemblages within the lake, (ii) to model the spatial variability of the diatom assemblages and their diversity, and (iii) to map the diatom distributions in the lake. A correspondence analysis (CA) separated the diatom assemblages into a planktonic and a periphytic group. Rheophilic taxa were found within the periphytic group. Variogram analysis showed that only the sample scores of the first CA axis and the Shannon diversity index were spatially structured. The range of spatial correlation was estimated to be 55 km for both variables. The diversity and, to a lesser extent, the sample scores had considerable small-scale variability of about 20 and 3%, respectively. Estimates of the first component of the CA and the Shannon index were derived using block-kriging. The maps of the estimates provided a basis for partitioning Lake Lama according to the spatial structures into an eastern and a western basin, a north–south connection between the basins, and a north–south directed tip at the far eastern end. It was shown that variation in diatom assemblages is mainly spatially structured at the catchment scale and that there is a considerable amount of variation at smaller scales. According to the modeled spatial distribution, the assemblages are most likely affected by the lake size, morphology, and the water and nutrient input introduced by rivers. This has to be taken into account when paleolimnological interpretations are drawn from records of complex lake systems like Lake Lama.  相似文献   

A method to reduce the influence of ice-rafted debris on a grain size record from northern Fram Strait, Arctic Ocean   总被引：2，自引：0，他引：2  

H. Christian Hass 《Polar research》2002,21(2):299-306

The granulometric composition of terrigenous deep-sea sediments provides information on current speed if certain frame conditions are fulfilled. These include that current transport is the only transport process. At high latitudes this type of investigation is impaired due to the influence of ice-rafted debris (IRD) which contaminates the current-sorted grain size fractions. This study presents a new method that addresses this problem by setting the ice-rafted sand in relation to the silt of both current- and ice-transported origin. Deviations from the resulting regression function are then used to determine the behaviour of the silt mean grain size as a function of current speed largely independent from IRD bias. The study is based on sediments from the Yermak Plateau, Arctic Ocean, a region influenced by IRD brought with the south-headed Transpolar Drift and by north-directed bottom currents. The IRD correction results in displaying changes of current speed at much higher clarity; climate forcing of the currents becomes more evident. For example, the 8200 year cold event shows up as a major event in the corrected record whereas it is hardly visible in the original record.  相似文献   

New palaeointensity results from Cretaceous basalt of Inner Mongolia, China     

Xixi Zhao  Peter Riisager  Ulrike Draeger  Zhong Zheng 《Physics of the Earth and Planetary Interiors》2004,141(2):131-140

We present new Thellier-Thellier palaeointensity results from three cooling units (32 samples) of Inner Mongolia lava flows (91.7 Ma) emplaced during the Cretaceous Normal Superchron (CNS). Based on rock-magnetic and microscopy observations the magneto-mineralogy of all samples is determined to be primary and unaltered high-Ti titanomagnetite. Accepted palaeointensity determinations, obtained in the 80-200 °C temperature interval, are of good technical quality with positive standard partial thermoremanent magnetisation (pTRM) checks and pTRM-tail checks. Obtained palaeointensity estimates range from 14.7 to 28.0 μT, with virtual axial dipole moments (VADM) of 2.4 to 4.6 (× 10²² Am²). The data agree well with recently published results from the same region and, combining the two datasets, we obtain independent estimates from six different cooling units yielding a time-averaged VADM of 3.2 ± 1.6 (× 10²² Am²). These data suggest a relatively low dipole moment towards the end of the Cretaceous Normal Superchron.  相似文献   

Microbial dechlorination of HCB,PCP, PCB180, HCH and PCE in a Yangtze Three Gorges Reservoir enrichment culture,China     

Irene Kranzioch-Seipel  Ulrike Beckert  Chaofeng Shen  Daqiang Yin  Andreas Tiehm 《Environmental Earth Sciences》2016,75(10):928

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Bristen granite: a highly differentiated,fluorite-bearing A-type granite from the Aar massif,Central Alps,Switzerland     

Kurt Bucher  Ulrike Seelig 《Swiss Journal of Geoscience》2018,111(1-2):317-340

Bristen granite is a body of fine-grained leucogranite occurring in the Gotthard rail base tunnel in the Central Alps. During construction of the tunnel, Bristen granite (Brgr) has been drilled along a 600 m long section. The aplite-granite belongs to the suite of Variscan granitoid intrusions of the Aar massif and contains a variety of accessory minerals typical of highly differentiated granites. Rock forming fluorite, partly enriched in yttrium (Y) and rare earth elements (REE), is intergrown with the late Y- and REE-bearing carbonate mineral synchysite. The granite contains a variety of Ti- and Y-REE-niobates, thorite, and zircon. Compared with the calc-alkaline central Aar granite (cAgr), Bristen granite is strongly depleted in Ti, P, Mg, Sr, and Ba and shows a remarkable enrichment in incompatible elements such as Rb, Th, U, Nb, Y, HREE and F. Bristen granite is the most evolved granitoid rock of the Aar massif. The composition of Brgr is typical of post-collisional reduced (ferroan) A-type granites. The Brgr melt formed in the lower crust and crystallized from a highly differentiated melt at the cotectic point in the quartz-feldspar system close to 100 MPa and 700 °C. The Brgr intruded as a small isolated stock pre-Variscan gneisses with sharply discordant contacts. The primary igneous host of Nb, Ta, Y, U, Th and REE is biotite in addition to minor amounts of allanite, and zircon. The presence of Y-REE-fluorite, synchysite, parisite and Y- and Ti-niobates and other REE-minerals can be related to reaction of igneous biotite and primary fluorite with hydrothermal fluids. The reaction is associated with alpine metamorphism, because Y-bearing fluorite and synchysite have been reported from Alpine fissures. The transformation of primary biotite to chlorite and muscovite released the heavy metal oxides under lower greenschist facies conditions that formed the Alpine diagnostic mineral stilpnomelane at about 300 °C.  相似文献   

Combined effects of pumped-storage operation and climate change on thermal structure and water quality     

Kobler  Ulrike Gabriele  Wüest  Alfred  Schmid  Martin 《Climatic change》2019,152(3-4):413-429

Climatic Change - The assessment of ecological impacts of pumped-storage (PS) hydropower plants on the two connected water bodies is usually based on present climatic conditions. However,...  相似文献   

The parametrization of the sulfate-nitrate-ammonia aerosol system in the long-range transport model EURAD     

I. J. Ackermann  H. Hass  M. Memmesheimer  C. Ziegenbein  A. Ebel 《Meteorology and Atmospheric Physics》1995,57(1-4):101-114

Summary Because of the obvious importance of aerosols for atmospheric modelling, an aerosol module has been developed as part of the European Acid Deposition Model (EURAD). The chemical and physical processes have been restricted to the sulfate-nitrate-ammonia system to study the influence of aerosols on acid deposition. Special consideration is given to the reversible formation process ofNH ₄ NO ₃ aerosols and the influence of the dissociation constant on the aerosol and gas phase concentrations. This component appears to be important in particular for regions where large ammonia emissions are found as in Europe.Concentration and deposition fields as predicted by EURAD are analysed for a simulation with and without the new aerosol module. Due to their smaller dry deposition velocities in the aerosol phase, the amount of nitrogen species in air is larger and the spatial distribution is considerably different if aerosols are taken into account. On the other hand wet deposition of nitrogen is enhanced due to the presence of easily soluble ammonium nitrate aerosols.A comparison with observations from the EMEP network has been conducted to evaluate the performance of the aerosol module. Modelling with the aerosol phase leads to a much better agreement between modelled and measured concentration fields.With 12 Figures  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