Preparation,collisional decay and transfer of alignment in C2H2 21

Stimulated Raman scattering is used to prepare ensembles of aligned acetylene molecules in thev ₂=1 excited vibrational level. Decay and transfer of the alignment is followed by laser induced fluorescence. Measurements of the initially excited alignment agree well with theoretical calculations. The rate constants for decay decrease as the rotational quantum numberJ of the excited level increases.     

National flood discharge mapping in Austria

This article presents the approach and the results of a study in which 30, 100 and 200 year return period flood discharges were estimated for 26,000 km of Austrian streams. Three guiding principles were adopted: combination of automatic methods and manual assessments by hydrologists to allow speedy processing and account for the local hydrological situation; combination of various sources of information including flood peak samples, rainfall data, runoff coefficients and historical flood data; and involvement of the Hydrographic Services to increase the accuracy and enhance the acceptance of results. The flood discharges for ungauged catchments were estimated by the Top-kriging approach with manual adjustment to the local flood characteristics. The adopted combination approach proved to be very efficient both in terms of the project time required and in terms of the accuracy and acceptability of the estimated flood discharges of given return periods.     

Multi-AUV Control and Adaptive Sampling in Monterey Bay

Operations with multiple autonomous underwater vehicles (AUVs) have a variety of underwater applications. For example, a coordinated group of vehicles with environmental sensors can perform adaptive ocean sampling at the appropriate spatial and temporal scales. We describe a methodology for cooperative control of multiple vehicles based on virtual bodies and artificial potentials (VBAP). This methodology allows for adaptable formation control and can be used for missions such as gradient climbing and feature tracking in an uncertain environment. We discuss our implementation on a fleet of autonomous underwater gliders and present results from sea trials in Monterey Bay in August, 2003. These at-sea demonstrations were performed as part of the Autonomous Ocean Sampling Network (AOSN) II project     

Multi-Scale Texture Modeling

Patterns of crystallographic preferred orientation are referred to as texture. The specific subject of texture analysis is the experimental determination and interpretation of the statistical distribution of orientations of crystals within a specimen of polycrystalline material, which could be metals or rocks. The objective is to relate an observed pattern of preferred orientation to its generating processes and vice versa. In geosciences, texture of minerals in rocks is used to infer constraints on their tectono-metamorphic history. Since most physical properties of crystals, such as elastic moduli, the coefficients of thermal expansion, or chemical resistance to etching depends on crystal symmetry and orientation, the presence of texture imparts directional properties to the polycrystalline material. A major issue of mathematical texture analysis is the resolution of the inverse problem to determine a reasonable orientation density function on SO(3) from measured pole intensities on , which relates to the inverse of the totally geodesic Radon transform. This communication introduces a wavelet approach into mathematical texture analysis. Wavelets on the two-dimensional sphere and on the rotational group SO(3) are discussed, and an algorithms for a wavelet decomposition on both domains following the ideas of Ta-Hsin Li is given. The relationship of these wavelets on both domains with respect to the totally geodesic Radon transform is investigated. In particular, it is shown that the Radon transform of these wavelets on SO(3) are again wavelets on . A novel algorithm for the inversion of experimental pole intensities to an orientation density function based on this relationship is developed.     

Hydrocarbon distribution in coals and in dispersed organic matter of different maceral compositions and maturities

More than 60 samples from 5 coal seams and adjacent siltstones and sandstones were selected from a well through Westphalian B sediments from Northern Germany in order to study bitumen generation and migration. The cores were drilled between 1200 und 1530 metres depth. In this interval, vitrinite reflectance (Rr) is increasing from 0.70 to 0.92%. Results reveal high hydrocarbon generation potentials for all coal samples, but not for adjacent clastic rocks, although maceral compositions of both are quite similar. Yields and compositions of thermal extracts from the coals depend on maceral compositions and rank. However, the bulk of the already generated bitumen has not been removed during natural coalification and is not easily releasable by thermovaporisation. A mass balance based on elemental composition of dull coals indicates that in the rather narrow rank interval (0.70–0.92% Rr) a total mass loss of 20% may have occurred by migration. This is evidenced by a loss of about 20% of the original hydrogen, the rest being stored in the coals.

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Zusammenfassung Um die Entstehung und Migration von Bitumen zu untersuchen wurden in Norddeutschland mehr als 60 Proben aus 5 Kohleflözen und benachbarten Silt- und Sandsteinen aus einer Bohrung durch Westphal B-Sedimente bearbeitet. Die Entnahmetiefe der Bohrkerne liegt zwischen 1200 und 1530 Metern. Innerhalb dieses Intervales steigt die Vitrinit-Reflexion (Rr) von 0,70 auf 0,92%. Für alle Proben aus den Flözen ergeben sich hohe Kohlenwasserstoff-Bildungspotentiale, nicht aber für die benachbarten klastischen Gesteine, obwohl die Mazeral-Zusammensetzungen in beiden ähnlich sind. Die Ausbeute und Zusammensetzung thermaler Extrakte aus den Flözen hängen von Mazeral-Zusammensetzung und Reife ab. Allerdings wurden weder während der Inkohlung größere Mengen des Bitumens abtransportiert, noch ist dieses durch Thermovaporisation leicht freisetzbar. Eine Massenbalanzierung auf der Basis der Elementzusammensetzung ergibt für das relativ schmale Interval von C,70-0,92% Rr ein Massenverlust von 20% durch Migration. Diese Angabe basiert auf einer 20%igen Reduzierung der ursprünglichen Wasserstoffmenge, wobei die restlichen 80% in der Kohle gespeichert bleiben.

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Résumé Dans un forage pratiqué à travers le Westphalien B du nord de l'Allemagne, on a sélectionné plus de 60 échantillons provenant de 5 couches de charbon ainsi que des siltites et grès adjacents, dans le but d'étudier la formation et la migration du bitume. Les carottes proviennent de profondeurs situées entre 1200 et 1530 m. Dans cet intervalle, le pouvoir réflecteur de la vitrinite (Rr) passe de 0,70 à 0,92%. L'étude révèle des potentiels élevés en hydrocarbure pour tous les échantillons de charbon, mais pas pour les roches détritiques voisines, bien que les compositions «macérales» soient analogues dans les deux cas. L'importance et la composition des extrait athermiques des charbons dépendent de la composition «macérale» et du degré d'évolution. Toutefois, la plus grande partie du bitume engendré est restée sur place au cours de la houillification naturelle et elle est difficile à extraire avex la methode de thermovaporisation. Une balance des masses d'éléments indique pour cet intervalle relativement étroit (0,7–0,92% Rr) une perte totale de masse de 20% due à la migration. Ce résultat correspond à une perte d'environ 20% de l'hydrogène originel, les 80% restants étant demeurés dans le charbon.

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60 5 , , . 1200 1530 . /Rr/ 0,7 0,92. , , . , , . , , . , , 20% 0,7 0,92 %. 20%; , 80%, .

     

Quantification of carbon flow from stable isotope fractionation in rice field soils with different organic matter content

Rice fields are an important source for the greenhouse gas methane produced by acetoclastic and hydrogenotrophic methanogenesis. Fractionation of ¹³C/¹²C can in principle be used to quantify the relative contribution of these pathways, but our knowledge of isotopic fractionation during reduction of CO₂ and turnover of acetate in different methanogenic environments is still scarce. We therefore measured δ¹³C signatures in two types of anoxic Italian rice field soils, one with high and one with low degradable organic matter (OM) content. Both soils were incubated in the presence and absence of methyl fluoride, a specific inhibitor of acetoclastic methanogenesis. Optimization of methyl fluoride concentration resulted in complete inhibition of acetoclastic methanogenesis. CH₄ was then exclusively produced by hydrogenotrophic methanogenesis, allowing determination of the isotopic signatures and fractionation factors specific for this methanogenic pathway. Acetate, which was then no longer consumed, accumulated and was used for determination of the isotopic signature of the fermentatively produced acetate (both total acetate and methyl carbon of acetate). Hence, all isotopic signatures, including fractionation factors were determined for the methanogenic soil. These data, were then used for computation of the relative contribution of the two methanogenic pathways. In the high OM soil, the contribution of acetoclastic methanogenesis to total CH₄ production increased simultaneously with decreasing acetate concentration. In the low OM soil, methanogenesis from H₂/CO₂ was clearly greater than theoretically expected. Furthermore, isotope fractionation of hydrogenotrophic methanogenesis indicated that the in situ energy status of methanogens strongly depended on the availability of organic carbon in the rice field soil system. Collectively, our data show that the study of isotopic fractionation in methanogenic environments allows a deeper insight into the ongoing processes, which may be quite different in the same ecosystem with different content of degradable OM.     

The Bayesian approach to an internally consistent thermodynamic database: theory, database, and generation of phase diagrams

An internally consistent thermodynamic dataset has been derived for 148 endmember phases (145 solids and 3 fluids) comprising the elements Li, Na, K, Be, Mg, Ca, Ti, Cr, Mn, Fe, Zn, Al, Si, C, H, and O. This has been achieved by simultaneous treatment of phase property (like standard enthalpy of formation, standard entropy, molar heat capacity, molar volume, thermal expansivity, bulk modulus etc.) and reaction reversal data by the Bayesian method. The theory underlying the approach, and the computational methods involved, are briefly outlined. (For the benefit of readers unfamiliar with inference statistics, the basic concepts of the Bayes method are also presented in such a way that they can be grasped intuitively.) Although not yet addressed, this method can be extended to refine the thermodynamic mixing properties of crystalline solutions. The sources of the input data, culled from the literature, are summarized in the Appendix. The resulting database is succinctly documented in this paper. It includes the enthalpies of formation and entropies, their uncertainties, and the correlation among them. The database allows calculation of P-T, T-X _CO2, P-X _CO2, and T-f _O2 sections, with error propagation into the computed phase diagrams on a routine basis. A user-friendly computer program has been written to generate such phase diagrams. It is public domain software. The software and the thermodynamic database (which includes a complete documentation of the thermodynamic data above and beyond those listed (Table 2, here) may be downloaded from the web site http://homepage.ruhr-uni-bochum.de/niranjan.chatterjee/Index.htm. Examples of computed phase diagrams are given to illustrate the quality of the data and the capabilities of the software. Received: 11 March 1998 / Accepted: 11 June 1998