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81.
Pale-blue to pale-green tourmalines from the contact zone of Permian pegmatites to mica schists and marbles from different localities of the Austroalpine basement units (Rappold Complex) in Styria, Austria, are characterized. All these Mg-rich tourmalines have small but significant Li contents, up to 0.29 wt% Li2O, and can be characterized as dravite, with FeO contents of ?~?0.9–2.7 wt%. Their chemical composition varies from X (Na0.67Ca0.19?K0.02?0.12) Y (Mg1.26Al0.97Fe2+ 0.36Li0.19Ti4+ 0.06Zn0.01?0.15) Z (Al5.31?Mg0.69) (BO3)3 Si6O18 V (OH)3? W [F0.66(OH)0.34], with a?=?15.9220(3), c?=?7.1732(2) Å to X (Na0.67Ca0.24?K0.02?0.07) Y (Mg1.83Al0.88Fe2+ 0.20Li0.08Zn0.01Ti4+ 0.01?0.09) Z (Al5.25?Mg0.75) (BO3)3 Si6O18 V (OH)3? W [F0.87(OH)0.13], with a?=?15.9354(4), c?=?7.1934(4) Å, and they show a significant Al-Mg disorder between the Y and the Z sites (R1?=?0.013–0.015). There is a positive correlation between the Ca content and?<?Y-O?>?distance for all investigated tourmalines (r?≈?1.00), which may reflect short-range order configurations including Ca and Fe2+, Mg, and Li. The tourmalines have XMg (XMg?=?Mg/Mg?+?Fetotal) values in the range 0.84–0.95. The REE patterns show more or less pronounced negative Eu and positive Yb anomalies. In comparison to tourmalines from highly-evolved pegmatites, the tourmaline samples from the border zone of the pegmatites of the Rappold Complex contain relatively low amounts of total REE (~8–36 ppm) and Th (0.1–1.8 ppm) and have low LaN/YbN ratios. There is a positive correlation (r?≈?0.91) between MgO of the tourmalines and the MgO contents of the surrounding mica schists. We conclude that the pegmatites formed by anatectic melting of mica schists and paragneisses in Permian time. The tourmalines crystallized from the pegmatitic melt, influenced by the metacarbonate and metapelitic host rocks.  相似文献   
82.
This paper provides the first measurements of the nitrogen (N) concentrations and isotopic compositions of high- and ultrahigh-pressure mafic eclogites, aimed at characterizing the subduction input flux of N in deeply subducting altered oceanic crust (AOC). The samples that were studied are from the Raspas Complex (Ecuador), Lago di Cignana (Italy), the Zambezi Belt (Zambia) and Cabo Ortegal (Spain), together representing subduction to 50-90 km depths. The eclogites contain 2-20 ppm N with δ15Nair values ranging from −1 to +8‰. These values overlap those of altered oceanic crust, but are distinct from values for fresh MORB (for the latter, ∼1.1 ppm N and δ15Nair ∼ −4‰). Based on N data in combination with other trace element data, the eclogite suites can be subdivided into those that are indistinguishable from their likely protolith, AOC, with or without superimposed effects of devolatilization (Lago di Cignana, Cabo Ortegal), and those that have experienced metasomatic additions during subduction-zone metamorphism (Zambezi Belt, Raspas). For the former group, the lack of a detectable loss of N in the eclogites, compared to various altered MORB compositions, suggests the retention of N in deeply subducted oceanic crust. The metasomatic effects affecting the latter group can be best explained by mixing with a (meta)sedimentary component, resulting in correlated enrichments of N and other trace elements (in particular, Ba and Pb) thought to be mobilized during HP/UHP metamorphism. Serpentinized and high-pressure metamorphosed peridotites, associated with the eclogites at Raspas and Cabo Ortegal, contain 3-15 ppm N with δ15Nair values ranging from +3 to +6‰, significantly higher than the generally accepted values for the MORB mantle (δ15Nair ∼ −5‰). Based on their relatively high N contents and their homogeneous and positive δ15N values, admixing of sedimentary N is also indicated for the serpentinized peridotites.One possible pathway for the addition of sediment-derived N into eclogites and peridotites involves mixing with fluids along the slab-mantle wedge interface. Alternatively, sedimentary N could be incorporated into peridotites during serpentinization at bending-related faults at the outer rise and, during later deserpentinization, released into fluids that then infiltrate overlying rocks. Deep retention of N in subducting oceanic crust should be considered in any attempt to balance subduction inputs with outputs in the form of arc volcanic gases. If materials such as these eclogites and serpentinized peridotites are eventually subducted to beyond sub-arc depths into the deeper mantle, containing some fraction of their forearc-subarc N inventory (documented here), they could deliver isotopically heavy N into the mantle to potentially be sampled by plume-related magmas.  相似文献   
83.
The Spessart district (SW Germany), located at the southwestern margin of the Permian Kupferschiefer basin in Central Europe, hosts abundant stratabound and structurally controlled base metal mineralization. The mineralization styles identified are (1) stratabound Cu-Pb-Zn-(Ag) ores in Zechstein sedimentary rocks, (2) structurally controlled Cu-As-(Ag) ores in Zechstein sedimentary rocks, (3) crosscutting Co-Ni-(Bi)-As and Cu-Fe-As veins, (4) stratabound metasomatic Fe-Mn carbonate ores in Zechstein dolomite, (5) barren barite veins, and (6) Fe-Mn-As veins in Permian rhyolites. Building on previous work that involved mineralogical, textural, and chemical characterization of the major mineralization types, we have performed a comprehensive sulfur isotope study that applied both conventional and novel laser-ablation multi-collector inductively coupled plasma mass spectrometry techniques. The δ34S values of sulfide minerals from the different ore types are consistently negative and highly variable, in the range between −44.5‰ and −3.9‰, whereas the δ34S values of barite are all positive in the range between 4.7‰ and 18.9‰. Remarkably, stratabound and structurally controlled mineralization in Zechstein sedimentary rocks has the least negative δ34S values, whereas vein-type deposits have consistently more negative δ34S values. The observed pattern of sulfide δ34S values can be best interpreted in terms of fluid mixing at the basement-cover interface. Hydrothermal fluids originating from the crystalline basement migrated upward along subvertical fault zones and were periodically injected into groundwaters that were flowing in the post-Variscan sedimentary cover. These groundwaters had interacted with the Zechstein sedimentary rocks, resulting in fluids characterized by elevated concentrations of reduced sulfur (with negative δ34S values) and alkaline pH. Repeated mixing between both chemically contrasting fluids caused rapid and efficient precipitation of sulfide ore minerals in hydrothermal veins with highly variable but distinctly negative δ34S values.  相似文献   
84.
A study to explain the emission of nitric oxide from a marsh soil   总被引:1,自引:0,他引:1  
In the period 18–21 September 1989, soil NO emission was studied at Halvergate Marshes, Norfolk (U.K.) within the framework of the BIATEX-LOVENOX joint field experiment. Using a dynamic chamber technique, 186 measurements at four plots were performed showing a net NO flux of 7.2–14.6×10–12 kgN m–2 s–1. Soil samples from a soil profile (1.0 m) at a representative site and from the uppermost layer (0.1 m) of each of the four plots were sent to the laboratory for (a) detailed physical and chemical soil analysis, (b) determination of NO production rates, NO uptake rate constants, and NO compensation mixing ratios, and (c) characterization of the microbial processes involved. A diffusive model (Galbally and Johansson, 1989) was applied to the laboratory results to infer NO fluxes of the individual soil samples. When we compared these fluxes with those measured in the field, we found agreement within a factor 2–4. Furthermore, laboratory studies showed, that NO was produced and consumed only in the upper soil layer (0–0.1 m depth) and that the NO production and consumption activities observed in the Halvergate marsh soil were most probably due to the anaerobic metabolism of denitrifying bacteria operating in anaerobic microniches within the generally aerobic soil.  相似文献   
85.
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   
86.
This paper discusses theory and results of an attempt to use non-linear programming methods to arrive at an optimal, in the sense of least cost, solution to the design of a survey system to meet specified accuracy. In other words, the method determines the combination of various types of observations which will yield the required accuracy of control points for a minimum cost. The theoretical background of the procedure is discussed, and methods of extension to photo-grammetry and other sciences are presented. Much of the paper is concerned with discussing results of numerical solutions for the optimal design of several small, but typical, mapping problems. It is believed that this research is original with the author, as extensive literature searches and correspondence has produced no knowledge of prior research into this application of nonlinear programming. The method at its current state of development appears to be capable of yielding significant improvements to the present concepts of survey network design.  相似文献   
87.
88.
Emission of nitrous oxide from temperate forest soils into the atmosphere   总被引:5,自引:0,他引:5  
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   
89.
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.

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90.
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. , .
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