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81.
The paper presents results of a parametric study of vertical oscillations of a flexible circular plate on the surface of an elastic half-space and an elastic layered system. The solution of the problem is based on the ‘ring method’. Vertical oscillations have been analysed to determine the displacement and soil reaction distributions at the soil-plate interface and the impedance functions. Parameters of the study include material and geometrical properties of a soil system and a plate and the load distribution on the plate. The results indicate significantly different behaviour of a flexible plate from that of a rigid one. Based on the observed behaviour, a classification of plates has been suggested. 相似文献
82.
83.
N2O emission rates were measured during a 13-month period from July 1981 till August 1982 with a frequency of once every two weeks at six different forest sites in the vicinity of Mainz, Germany. The sites were selected on the basis of soil types typical for many of the Central European forest ecosystems. The individual N2O emission rates showed a high degree of temporal and spatial variabilities which, however, were not significantly correlated to variabilities in soil moisture content or soil temperatures. However, the N2O emission rates followed a general seasonal trend with relatively high values during spring and fall. These maxima coincided with relatively high soil moisture contents, but may also have been influenced by the leaf fall in autumn. In addition, there was a brief episode of relatively high N2O emission rates immediately after thawing of the winter snow. The individual N2O emission rates measured during the whole season ranged between 1 and 92 g N2O-N m–2 h–1. The average values were in the range of 3–11 g N2O-N m–2 h–1 and those with a 50% probability were in the range of 2–8 g N2O-N m–2 h–1. The total source strength of temperate forest soils for atmospheric N2O may be in the range of 0.7–1.5 Tg N yr–1. 相似文献
84.
In the coal-mining Ruhr-area, Upper Carboniferous rocks (ca. 4000 m) consist of interlayered sandstones, siltstones, mudstones and coals. They were deposited in a tropical, paralic environment where alternating fluvial sedimentation, occasional marine ingressions, and swamp growth resulted in an irregular cyclic succession. The total sedimentary package contains on an average 6 Vol.-% of organic matter. About 70 Vol.-% of the organic matter occurs in coal seams, the rest as dispersed organic matter in clastic rocks. The organic matter is autochthonous in the coals and allochthonous in associated sandstones and siltstones. It consists of about 70% vitrinite, 20% inertinite, and 10% liptinite. The overall maceral group composition is the same for coals and dispersed organic matter. This surprising similarity is caused by a nearly exclusive input of land-plant derived organic matter to swamps and fluvial systems and a similar degree of preservation. Highest average liptinite contents (% of total macerals) were found in unrooted mudstones, highest average inertinite contents in coarse-grained siltstones and highest average vitrinite percentages in sandstones.Maturities of the sediments studied are well within the hydrocarbon generation window, e. g. vitrinite reflectivities range from 0.6% to 1.6%. Reflectivities measured on dispersed particles in clastic rocks are similar to those measured in coal seams. Calculations of the amount of methane generated indicate that coal seams contributed more to the total hydrocarbon generation than dispersed organic matter.
Zusammenfassung Das Oberkarbon des Ruhrgebietes besteht aus ca. 4000 Metern wechsellagernder Sandsteine, Siltsteine und Kohleflöze. Der Ablagerungsraum der Sedimente war eine Region mit tropischem Klima, genauer ein paralisches Environment mit unregelmäßig alternierenden Folgen von fluviatilen Sedimenten, marinen Transgressionen und verbreiteten Sumpfablagerungen. Der Anteil organischer Substanzen an der gesamten Sedimentmenge beträgt durchschnittlich 6%. 70% dieser organischen Masse ist in Kohleflözen angereichert, der Rest liegt verteilt in den klastischen Gesteinen vor. Die Herkunft der organischen Substanz in den Kohleflözen ist autochthon, die in den benachbarten Sand- und Siltsteinen allochton. Die Zusammensetzung des organischen Materials ist 70% Vitrinit, 20% Inertinit und 10% Liptinit. Die allgemeine Zusammensetzung nach Mazeral-Gruppen ist für die Kohleflöze und das verteilte Material in den Nachbargesteinen identisch. Diese Ähnlichkeit beruht auf der gemeinsamen Herkunft der organischen Substanz in Sümpfen und Flußsystemen, die fast ausschließlich von Landpflanzen bestimmt wird, und einer sich entsprechenden Konservierung.Der Reifegrad der analysierten Sedimente liegt innerhalb des Kohlenwasserstoff-Bildungsbereiches (die Vitrinit-Reflexionen reichen von 0,6–1,6%). Dabei entsprechen die in den klastischen Gesteinen beobachteten Reflexionswerte weitgehend denen der Kohleflöze. Anhand der Menge des erzeugten Methans läßt sich erkennen, daß der Anteil der Kohleflöze an der Kohlenwasserstoff-Produktion höher ist als der Anteil, den disperse organische Substanzen der Klastika beisteuern.
Résumé Dans la région minière de la Ruhr, le Carbonifère supérieur constitue une succession, épaisse de 4.000 m environ, de grès, de siltites et de charbon. Leur dépôt, dans un milieu paralique tropical, a été marqué par des alternances de sédimentation fluiviale, de transgressions marines occasionnelles, et d'épisodes marécageux; il en résulte une disposition cyclique irrégulière. La série sédimentaire contient dans l'ensemble 6% de matière organique en moyenne. Environ 70% de cette matière organique se trouve dans les couches de charbon où elle est autochtone; le reste est allochtone et dispersé dans les grès et siltites. La matière organique se répartit approximativement en 70% de vitrinite, 20% d'inertinite et 10% de liptinite. La composition moyenne du groupe «macéral» est la même pour les charbons et la matière organique dispersée. Cette identité surprenante est l'expression d'une alimentation provenant exclusivement de plantes terrestres et d'un même degré de conservation.La maturité des sédiments étudiés se situe à l'intérieur du domaine de genèse des hydrocarbures: le pouvoir réflecteur de la vitrinite s'échelonne entre 0,6% et 1,6%. Les gradients du pouvoir réflecteur observés dans les roches détritiques et dans les couches de charbon sont analogues. Le calcul de la quantité de méthane engendré indique que la contribution des couches de charbon à la production totale d'hydrocarbure est supérieur à celle de la matière organique dispersée.
4000 , . , , . 6%.70 % , . , — . 70 % , 20% 10% . . ; . ; 0,6 1,0, . , , , .相似文献
85.
The volcanogenic exhalative Tverrfjell deposit occurs in a sequence of predominantely mafic submarine meta-volcanics, interlayered with geosynclinal pelitic sediments, turbidites and volcanic breccias, belonging to the Early Cambrian to Early Arenigian Støren Group. Two major deformational phases and low to medium grade metamorphic conditions are recognized in the study area. Basalts are mainly tholeiitic but alkaline types occur as well. Extensive fractionation produced highly evolved basalts and even andesites. Basalt compositions are comparable to Type II-ocean floor basalt. The copper/zinc ores of the Tverrfjell deposit are strictly confined to an andesitic extrusive body. An extensive magma chamber is postulated to explain magma fractionation, and as a heat source that generated the exhalative Tverrfjell ore body. It is suggested that the deposit was formed at an intraplate volcanic center or back-arc spreading center.
Zusammenfassung Die vulkanogen-exhalativ gebildete Tverrfjell-Lagerstätte befindet sich innerhalb einer Abfolge überwiegend mafischer, submariner Metavulkamte, die mit geosynklinalen pelitischen Sedimenten, Turbiditen und vulkanischen Brekkzien wechsellagern. Diese Gesteine gehören zur Støren-Gruppe, die vom Unterkambrium bis zum frühen Arenig reicht. Zwei Hauptdeformationsphasen in Verbindung mit niedrig bis mittelgradiger Metamorphose können im Arbeitsgebiet nachgewiesen werden. Die Basalte sind zumeist tholeiitisch, jedoch treten auch alkalibasaltische Typen auf. Durch starke Fraktionierung sind hoch entwikkelte Basaltmagmen und sogar Andesite entstanden. Die Basalte können mit Typ II-Ozeanbodenbasalten verglichen werden. Die Kupfer/Zinkerze der Tverrfjell-Lagerstätte sind strikt an einen andesitischen Extrusivkörper gebunden. Eine ausgedehnte Magmenkammer wird postuliert, in welcher die Magmenfraktionierung stattfand, und die als Wärmequelle für die Bildung des Tverrfjellerzkörpers angesehen wird. Aufgrund der Untersuchungsergebnisse wird angenommen, daß die Lagerstätte in einem Intraplatten-Vulkanzentrum oder in einem Back-arc spreading centre gebildet wurde.
Résumé Le gisement volcanogénétique exhalatif du Tverrfjell se trouve au sein d'une série de métavolcanites sous-marines, surtout basiques, qui alternent avec des pélites géosynclinales, des turbidites et des brèches volcaniques. Ces roches appartiennent au groupe de Støren qui s'étend du Cambrien inférieur jusqu'à l'éo-Arénigien. Dans cette région, deux phases déformatives majeures ont été reconnues, liées à un métamorphisme de degré faible à moyen.La plupart des basaltes sont de type tholéiitique, mais il existe aussi des basaltes alcalins. Un fractionnement poussé a engendré magmas basaltiques très évolués et même des andésites. Les compositions des basaltes sont comparables à celles du «basalte océanique de type II». La minéralisation en Cu-Zn de Tverrfjell est liée strictement à une masse extrusive andésitique. Pour expliquer le fractionnement magmatique, on admet l'existence d'une de chaleur lors de la formation du gisement de Tverrfjell. Ce gisement a dû se former soit dans un centre volcanique intraplaque, soit dans une zone d'expansion d'arrière-arc.
- Tvenfjell . . , , . Støren, . , . , . , . . . , , Tverrfjell'e. , .相似文献
86.
Thomas Stachel Sonja Aulbach Gerhard P. Brey Jeff W. Harris Ingrid Leost Ralf Tappert K.S. Viljoen 《Lithos》2004,77(1-4):1-19
On a global scale, peridotitic garnet inclusions in diamonds from the subcratonic lithosphere indicate an evolution from strongly sinusoidal REEN, typical for harzburgitic garnets, to mildly sinusoidal or “normal” patterns (positive slope from LREEN to MREEN, fairly flat MREEN–HREEN), typical for lherzolitic garnets. Using the Cr-number of garnet as a proxy for the bulk rock major element composition it becomes apparent that strong LREE enrichment in garnet is restricted to highly depleted lithologies, whereas flat or positive LREE–MREE slopes are limited to less depleted rocks. For lherzolitic garnet inclusions, there is a positive relation between equilibration temperature, enrichment in MREE, HREE and other HFSE (Ti, Zr, Y), and decreasing depletion in major elements. For harzburgitic garnets, relations are not linear, but it appears that lherzolite style enrichment in MREE–HREE only occurs at temperatures above 1150–1200 °C, whereas strong enrichment in Sr is absent at these high temperatures. These observations suggest a transition from melt metasomatism (typical for the lherzolitic sources) characterized by fairly unfractionated trace and major element compositions to metasomatism by CHO fluids carrying primarily incompatible trace elements. Melt and fluid metasomatism are viewed as a compositional continuum, with residual CHO fluids resulting from primary silicate or carbonate melts in the course of fractional crystallization and equilibration with lithospheric host rocks.
Eclogitic garnet inclusions show “normal” REEN patterns, with LREE at about 1× and HREE at about 30× chondritic abundance. Clinopyroxenes approximately mirror the garnet patterns, being enriched in LREE and having chondritic HREE abundances. Positive and negative Eu anomalies are observed for both garnet and clinopyroxene inclusions. Such anomalies are strong evidence for crustal precursors for the eclogitic diamond sources. The trace element composition of an “average eclogitic diamond source” based on garnet and clinopyroxene inclusions is consistent with derivation from former oceanic crust that lost about 10% of a partial melt in the garnet stability field and that subsequently experienced only minor reenrichment in the most incompatible trace elements. Based on individual diamonds, this simplistic picture becomes more complex, with evidence for both strong enrichment and depletion in LREE.
Trace element data for sublithospheric inclusions in diamonds are less abundant. REE in majoritic garnets indicate source compositions that range from being similar to lithospheric eclogitic sources to strongly LREE enriched. Lower mantle sources, assessed based on CaSi–perovskite as the principal host for REE, are not primitive in composition but show moderate to strong LREE enrichment. The bulk rock LREEN–HREEN slope cannot be determined from CaSi–perovskites alone, as garnet may be present in these shallow lower mantle sources and then would act as an important host for HREE. Positive and negative Eu anomalies are widespread in CaSi–perovskites and negative anomalies have also been observed for a majoritic garnet and a coexisting clinopyroxene inclusion. This suggests that sublithospheric diamond sources may be linked to old oceanic slabs, possibly because only former crustal rocks can provide the redox gradients necessary for diamond precipitation in an otherwise reduced sublithospheric mantle. 相似文献
87.
Distribution of polycyclic musks in water and particulate matter of the Lippe River (Germany) 总被引：3，自引：0，他引：3
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
88.
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
89.
90.