Changes in the water regime of the caspian sea

The article deals with issues of structure and dynamics of the Caspian Sea water balance. On the base of historical, paleogeomorphological and other data the evolution history of the Caspian Sea and its basin has been observed for different time intervals down to 400 thous. years ago. Presented are computerized data on water balance components in the current centenary obtained from instrumental observations, revealed are causes of the sea-level fluctuations within that time interval and anthropogenic factor contribution to this process. Based on the analysis of this material, an attempt has been undertaken to present a scenarion of a possible sea-level position of the Caspian Sea with the expected versions of climatic changes at the end of the XX and beginning of the XXI centuries.     

Über stratigraphische Untersuchungsmethoden in rezenten Tiefseesedimenten

Zusammenfassung Durch Bestimmung der Foraminiferenanzahl in I g Sediment wird die biostratigraphische Untersuchungsmethode, die mittels einer qualitativen und quantitativen Erfassung der Foraminiferenfauna in den Tiefseekernen der deutschen Meteor-Expedition und schwedischen Albatroß-Expedition durchgeführt werden ist, auf ihre Richtigkeit hin geprüft. Die Untersuchung hat die Anwendbarkeit dieser stratigraphischen Methode bestätigt. Sie hat daneben wiederum gezeigt, daß die Verbreitung und Entwicklung der einzelnen Foraminiferenarten vor allem von der Temperatur des Meerwassers abhängig sind; andere Faktoren wie Phosphatgehalt des Wassers usw. scheinen in dieser Hinsicht eine mehr untergeordnete Rolle zu spielen. Unter gewissen Voraussetzungen können Tiefseekerne durch Bestimmung der Foraminiferenanzahl je 1 g Sediment in groben Zügen stratigraphisch gegliedert werden; auch kann die Individuenanzahl der einzelnen Foraminiferenarten aus der Foraminiferenanzahl in 1 g Sediment und aus der prozentualen Zusammensetzung der Gesamtfauna errechnet werden. Mit den hier gewonnenen Erkenntnissen wird versucht, die engen Bezichungen zwischen dem prozentualen Anteil der Warmwasserforaminiferen in der Gesamtfauna und dem CO₂-Gehalt des Sedimentes, dieOvey im Kern 241 der schwedischen Albatroß-Expedition beobachtet hat, zu deuten.Herrn Professor Dr.Carl W. Correns zum 60. Geburtstag gewidmet.     

Spatial variations in the progress of land reform in Romania

Romania's socialist agricultural sector has been transformed by a series of measures taken after the revolution of 1989. A new farm structure is emerging out of the restitution provided for under the Land Law of 1991. There are striking spatial variations in different aspects of the privatisation process, especially the contrasting situations between the hill country (with heavy pressure on land) and the plains (where there is much better supply in relation to demand). Very small units of land ownership are being grouped into larger functional units for management by associations which are especially prominent in the main cropping zones. Meanwhile individual smallholdings are predominant in the hill and mountain zones. Despite a desire for owner-occupation, association is often advantageous through efficient deployment of machinery and some 40 percent of land allocated to individual peasants is being worked by some 20,000 associations. However, the situation has not yet stabilised and it is emphasised that small farms should be regarded not simply as agricultural units but as the cores of diversified enterprises characterised increasingly by pluriactivity     

Diffractometric clay mineral analysis of Recent sediments of Lake Constance (Central Europe)

Mica, smectite, and chlorite are the characteristic clay minerals in about 120 Recent sediment samples of Lake Constance as shown by semiquantitative clay mineral analysis. Interstratified clay minerals are practically absent, kandites were not found.The decrease of the smectite/mica ratio from West to East is apparently due to the dominance of the mica-chlorite assemblage of the Rhine river derived from the northern Alps in the eastern part of the lake. With increasing distance from the delta of the Rhine river, the Tertiary Molasse clay minerals (mainly mica and smectite) derived from rocks surrounding the lake become more abundant.

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Zusammenfassung An 120 Sedimentproben aus dem Bodensee wurde der Tonmineralbestand der Fraktion <2 durch die röntgenographische Phasenanalyse halbquantitativ ermittelt.Glimmer, Smectit und Chlorit sind die charakteristischen Tonmineralgruppen in den Sedimenten. Mixed-layer-Minerale treten so gut wie nicht auf, Kandite konnten nicht nachgewiesen werden.Aus der Bestimmung der relativen Häufigkeit von Glimmer und Smectit ergibt sich, daß das Smectit/Glimmer-Verhältnis von Osten (Einmündung des Alpenrheins) nach Westen ständig zunimmt.Diese Verteilung ist durch die Zufuhr von Glimmer und Chlorit durch den Alpenrhein aus den nördlichen Alpen bedingt, die jedoch mit zunehmender Entfernung vom Delta durch die Molasse-Distributiv-Provinz mit vorherrschend Glimmer und Smectit überlagert wird.

     

Recent variations in the general circulation as related to glacier retreat in northern Scandinavia

Summary A review is given of the investigations on variations in the general circulation in middle latitudes made byWillett andPetterssen. According toWillett a «high-index» type of circulation pattern with a strong zonal flow has probably caused the recent climatic improvement in the northern latitudes while the «low-index» type with meridional flow would create a cooling off in the same areas. According toPetterssen an other type of «low-index» pattern with a weak zonal flow and strong meridional exchange of air has been the essential cause of the warming up of the northern latitudes in Europe. This implies that the definition of the «low-index» type is not clear and gives rise to misunderstanding. Making use of our experience on glacier retreat in northern Scandinavia it is concluded that thePetterssen type of circulation more probably than the «high-index» type has caused the warming-up in the North Atlantic area from which the retreat of the glaciers has followed.     

Imagery in the Presence of Turbulence Using Slit Aperture Telescope With Partial Adaptive Corrections

The objective of this communication is to study and totest numerically the concept of partial adaptive correction with arotating Slit Aperture Telescope (SAT). After a brief summary of theprinciple of image reconstruction with the rotating SAT operating withoutthe atmospheric turbulence, we describe the simulations of imagereconstruction when a partial atmospheric correction is performed in onedimension only, along the long axis of the rotating SAT. Thereconstruction algorithm performs the inversion of the Radon transform.The SAT can use a small adaptive optics system with far fewer actuatorsthan conventional two-dimensional devices, but a relatively high degree ofone-dimensional correction is needed to recover a satisfactorytwo-dimensional image. The effect of additive noise on the reconstructedimage is also investigated.     

On the distribution of rainfall over the Sultanate of Oman

Rainfall distribution over the Sultanate of Oman is analysed. Data from seven recently installed weather stations as well as supporting data from scattered sources were used. Distribution maps were drawn. NW and NE winter wind meet resulting in troughs and rainfall on the Mountains and Coastal Strips. Summer monsoon wind dominates the S. Central areas of overlap receive light showers from both summer monsoons and winter local troughs. Heavier amounts of rainfall are generally associated with high altitude.     

Crystal structure refinement of hendricksite,A Zn- and Mn-rich trioctahedral potassium mica: A contribution to the crystal chemistry of zinc-bearing minerals

Summary The crystal structure of hendricksite, a trioctahedral mica of biotite type, characterized by high Zn²⁺ and Mn²⁺ contents has been refined by least square methods. The structural formula is: (K_0.89Na_0.10Ba_0.04)(Mg_1.57Zn_0.54Mn _0.40 ²⁺ Fe _0.25 ²⁺ Al_0.07Ti_0.07Cr_0.01)(Si_2.92Al_1.08)O₁₀ (OH)₂. The space group isC2/m and the cell parameters are:a=5.340(2) Å,b=9.524(2) Å,c=10.235(3) Å, =100.07(2)^o, the cell volume isV=497.98 ų. The final unweightedR=0.072. Average cation-anion distances in polyhedra are: T–O=1.659 Å, M(1)–O=2.093 Å, M(2)–O=2.088 Å, A–O_long=3.316 Å and A–O_short=3.004 Å; A is the alkaline cation. The rotation angle of tetrahedra is =6.7°. The analysis of electron densities, of the dimensions and distorsions of polyhedra shows that Zn²⁺ is exclusively in octahedral sites; there is no order between six-fold coordinated cations. A comparison between the structural features of hendricksite and those of the two main end-members of biotites, phlogopite and annite, is presented.The effect of the strong covalence of Zn–O bonds is particularly visible on the dimensions and orientations of the thermal ellipsoids of octahedral sites M(1) and M(2) which contain zinc. In all the published structures of trioctahedral micas, the ellipsoids of cationic sites are uniaxial positive, elongated parallel toc ^*. In hendricksite, this is observed only for the two zinc-free sites (T and A; in the octahedra M(1) and M(2), which contain zinc, the ellipsoids are approximately uniaxial negative, flattened parallel toa, which is a unique situation.Zinc which habitually favours the tetrahedral coordinations with oxygen, enters the octahedra only, i.e. the chemically anisotropic sites, in hendricksite. The strong polarizability of Zn²⁺ is proposed to explain this behaviour.An examination of the behaviour of Zn²⁺ in other compounds shows that this situation is general, zinc favours chemically anisotropic sites and specially those adjacent to OH or H₂O.

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Affinement de la structure cristalline de la hendricksite, mica trioctaédrique potassique riche en Zn et Mn; une contribution à la connaissance cristallochimique des minéraux zincifères

Résumé On a affiné par moindres carrés la structure de la hendricksite, mica trioctaédrique de type biotite, caractérisé par une teneur élevée en Zn²⁺ et Mn²⁺. La formule structurale de ce mica est: (K_0m89Na_0,10Ba_0,04)(Mg_1,57Zn_0,54Mn _0,40 ²⁺ Fe _0,25 ²⁺ Al_0,07Ti_0,07Cr_0,01)(Si_2,92Al_1,08)O₁₀(OH)₂. Le groupe spatial estC2/m et les paramètres de la maille:a=5,340(2) Å,b=9,254(2) Å,c=10,235(3) Å, =100,07(2)°; le volume de la maille estV=497,98 ų. Le résidu final non-pondéré estR=0,072. Les distances cation-anion moyennes dans les polyèdres sont les suivantes: T–O=1,659 Å, M(1)–O=2,093 Å, M(2)–O=2,088 Å, A–O_long=3,316 Å et A–O_court=3,004 Å où A désigne le cation alcalin. L'angle de rotation tétraédrique, =6,7°, est très semblable à celui de la phlogopite. L'analyse des densités électroniques, des dimensions et distorsions des polyèdres montre que Zn²⁺ est exclusivement en coordinance octaédrique et qu'il n'y a pas d'ordre entre les cations hexacoordonnés. On présente une comparaison des caractères structuraux de la hendricksite avec ceux des deux principaux pôles des biotites, la phlogopite et l'annite.L'effet de la forte covalence de la liaison Zn–O est particulièrement visible sur les dimensions et orientations des ellipsoides d'agitation thermique des deux sites octaédriques, sites zincifères. Dans toutes les structures de micas trioctaédriques publiées, les ellipsoides des sites cationiques sont uniaxes positifs, allongés parallèlement àc ^*, ce qui s' observe effectivement dans les deux sites non-zincifères (T et A) de la hendricksite, par contre, dans les octaèdres M(1) et M(2), qui contiennent le zinc, les ellipsoides sont approximativement uniaxes négatifs, applatis parallèlement àa, ce qui est une situation unique.Le zinc, qui se fixe généralement en sites tétraédriques dans les structures de type oxyde, occupe les sites octaédriques, c'est-à-dire les sites chimiquement anisotropes dans la hendricksite. La forte polarisabilité de Zn²⁺ est proposée pour expliquer ce comportement.Un examen du comportement de Zn²⁺ dans d'autres phases montre que cette situation est tout à fait générale, le zinc privilégiant les sites chimiquement anisotropes et en particulier ceux adjacents à OH où H₂O.