Jets

This is a discussion of concentrated large-scale flows in planetary atmospheres and oceans, argued from the viewpoint of basic geophysical fluid dynamics. We give several elementary examples in which these flows form jets on rotating spheres. Jet formation occurs under a variety of circumstances: when flows driven by external stress have a rigid boundary which can balance the Coriolis force, and at which further concentration can be caused by the beta effect; when there are singular lines like the line of vanishing windstress or windstress-curl, or the Equator; when compact sources of momentum, heat or mass radiate jet-like beta plumes along latitude circles; when random external stirring of the fluid becomes organized by the beta effect into jets; when internal instability of the mass field generates zonal flow which then is concentrated into jets; when bottom topographic obstacles radiate jets, and when frontogenesis leads to shallow jet formation. Essential to the process of jet formation in stratified fluids is the baroclinic life cycle described in geostrophic turbulence studies; there, conversion from potential to kinetic energy generates eddy motions, and these convert to quasibarotropic motions which then radiate and induce jet-like large-scale circulation. Ideas of potential vorticity stirring by eddies generalize the notion of Rossby-wave radiation, showing how jets embedded in an ambient potential vorticity gradient (typically due to the spherical geometry of the rotating planet) gain eastward momentum while promoting broader, weaker westward circulation. Homogenization of potential vorticity is an important limit point, which many geophysical circulations achieve. This well-mixed state is found in subdomains of the terrestrial midlatitude oceans, the high-latitude circumpolar ocean, and episodically in the middle atmosphere. Homogenization expels potential vorticity gradients vertically to the top and bottom of the fluid, and sideways to the edges of flow domains or gyres; in both these ways is jet formation enhanced.     

Reducibility behavior of polynomials with varying coefficients

LetK be a number field, and leth∈K[Y] be a polynomial of degreen. Fix an integer 0≤i≤n and compare the set ν of those integersa ofK such thath(Y)−aY ⁱhas a root inK with the set of those integersa, such thath(Y)−aY ⁱis reducible overK. Ifi is coprime ton, then we classify the rare cases where ν is not cofinite in . The main tools are a theorem of Siegel about integral points on algebraic curves and the theory of finite groups.     

Probing Higgs boson — and supersymmetry-induced CP violation in top quark production by (un-) polarized electron-positron collisions

We consider, both for unpolarized and longitudinally polarized electron beams, the reaction $e^ + e^ - \to t\bar t$ with subsequent semileptonict and nonleptonic $\bar t$ decay and vice versa and investigate optimized angular correlations which are sensitive to CP non-conservation in the $t\bar t$ production vertex. We calculate these correlations for two-Higgs-doublet extensions and the minimal super-symmetric extension of the Standard Model (SM) with CP violation beyond the Kobayashi-Maskawa phase. While the sensitivity of the optimal correlation for tracing dispersive CP effects is enhanced with longitudinally polarized electron beams, we find that the sensitivity of the best correlation for probing absorptive CP effects is almost independent of the polarization degree.     

Bivoltametric titrations using electrodes with innovative geometry

Electrodes with different surface areas were investigated for the determination of reversible, quasireversible, irreversible or electroinactive substrates. Two kinds of electrodes were constructed, a helical electrode with a given asymmetry and a platinum array electrode with a variable area. These electrodes were applied for the cerimetry of ammonium iron(II) sulfate and for the bromatometry of various organic substances. The theoretically derived effects on the shape of the voltametric titration curve are verified experimentally. It is possible to sharpen one side of the peak and to broaden the other side, depending on the system and the side of the peak one is interested in. It is possible to improve the bivoltametric determination of hydroquinone, benzocaine and sulfaguanidine by bromatometry by the directed employment of electrodes of different areas. For the bromatometric determination of electrochemically irreversible substrates the use of the electrode geometries proposed is a way to obtain a sharp bend and a steep decrease of titration curves with low values of the constant current which is a basic requirement for the accuracy.     

On noise reduction methods for chaotic data

Recently proposed noise reduction methods for nonlinear chaotic time sequences with additive noise are analyzed and generalized. All these methods have in common that they work iteratively, and that in each step of the iteration the noise is suppressed by requiring locally linear relations among the delay coordinates, i.e., by moving the delay vectors towards some smooth manifold. The different methods can be compared unambiguously in the case of strictly hyperbolic systems corrupted by measurement noise of infinitesimally low level. It was found that all proposed methods converge in this ideal case, but not equally fast. Different problems arise if the system is not hyperbolic, and at higher noise levels. A new scheme which seems to avoid most of these problems is proposed and tested, and seems to give the best noise reduction so far. Moreover, large improvements are possible within the new scheme and the previous schemes if their parameters are not kept fixed during the iteration, and if corrections are included which take into account the curvature of the attracting manifold. Finally, the fact that comparison with simple low-pass filters tends to overestimate the relative achievements of these nonlinear noise reduction schemes is stressed, and it is suggested that they should be compared to Wiener-type filters.     

On the formation of the [M ? OH]+ ion in m-nitrobenzaldoxime. evidence for a cyclohexadiene-type intermediate ion

In m-nitrobenzaldoxime a strongly enhanced loss of OH? is observed as compared with the p-nitro compound. Evidence is presented for a fragmentation mechanism involving the formation of a cyclohexadiene-type intermediate ion formed by a rearrangement of the hydroxyl hydrogen to the phenyl ring.     

Zdanovskii’s Rule and Isopiestic Measurements Applied to Synthetic Bayer Liquors

Isopiestic measurements of mixed electrolyte solutions involving sodium hydroxide and other components of Bayer liquors were performed at 50?°C and 100?°C. Most of the systems studied obey Zdanovskii’s rule exactly or very closely. However, those with sodium chloride as one of their components show deviations from Zdanovskii’s rule, which are well predicted by our thermodynamic modelling software based on Pitzer’s equations.     

Approximate molecular orbital theory: the ese mo formalism.: III. Parametrization for all- or valence-electron calculation using accurate STF bases for molecules containing 1st, 2nd,and 3rd row atoms. SO2 results

The key components of a completely theoretical parametrization of the essential-structural-elements molecular orbital (ESE MO) formalism using Slater-type AO basis in the LCAO SCF procedure are discussed. Special attention is paid to the problem of separability into core and valence parts of the total molecular wavefunction, including the case where valence functions strongly overlap neighbouring core orbitals. The use of Huzinaga and Cantu effective hamiltonian is proposed. The parametrization is tested in relation to the SO₂ molecules. The role of sulphur 3d functions in bonding as predicted by the present ESE MO calculations and ab initio calculations are compared. The present parametrization appears to adequately handle both the core/valence separation, and the diffuse higher valence sulphur 3d functions in this system.