Approaches to sharing knowledge in group problem structuring

Problem-structuring techniques are an integral aspect of ‘Soft-OR’. SSM, SAST, Strategic Choice, and JOURNEY Making, all depend for their success on a group developing a shared view of a problem through some form of explicit modelling. The negotiated problem structure becomes the basis for problem resolution. Implicit to this process is an assumption that members of the group share and build their knowledge about the problem domain. This paper explores the extent to which this assumption is reasonable. The research is based on detailed records from the use of JOURNEY Making, where it has used special purpose Group Support software to aid the group problem structuring. This software continuously tracks the contributions of each member of the group and thus the extent to which they appear to be ‘connecting’ and augmenting their own knowledge with that of other members of the group. Software records of problem resolution in real organisational settings are used to explore the sharing of knowledge among senior managers. These explorations suggest a typology of knowledge sharing. The implications of this typology for problem structuring and an agenda for future research are considered.     

Nourdin–Peccati analysis on Wiener and Wiener–Poisson space for general distributions

Given a reference random variable, we study the solution of its Stein equation and obtain universal bounds on its first and second derivatives. We then extend the analysis of Nourdin and Peccati by bounding the Fortet–Mourier and Wasserstein distances from more general random variables such as members of the Exponential and Pearson families. Using these results, we obtain non-central limit theorems, generalizing the ideas applied to their analysis of convergence to Normal random variables. We do these in both Wiener space and the more general Wiener–Poisson space. In the former space, we study conditions for convergence under several particular cases and characterize when two random variables have the same distribution. In the latter space we give sufficient conditions for a sequence of multiple (Wiener–Poisson) integrals to converge to a Normal random variable.     

Photoassociation Spectroscopy: Determination of Parameters of Potentials of Diatomic Molecules

Laser-induced fluorescence studied with the help of a tunable dye laser is used to record the photoassociation spectrum of equilibrium mercury atoms in the range of 34 700–37 300 cm^–1. The so-called Franck-Condon structure, which represents periodic variations of absorption intensity on a continuous background, is observed. The structure makes it possible to determine spectroscopic parameters of the upper bound potential and the lower repulsive potential, including the potential with a shallow Van der Waals well. The Numerov-Cooley procedure is used to find the numerical solution of the boundary problem, namely, eigenfunctions and eigenvalues of the Schrödinger equation for the one-dimensional motion in a potential field, matrix elements of transitions and partial waves, and the absorption spectrum of collisional pairs of atoms are calculated. The absorption spectrum of mercury dimers was simulated taking into account 100 vibrational and 200 rotational levels. The comparison of theoretical and experimental spectra according to Tellinghuisen made it possible to determine the lower part of the potential curve for the dimer excited state.     

Van der Waals molecules and collision pairs of noble-gas atoms ahead of a shock wave front

The effect of creation of an excess concentration of free electrons in an anomalously thick layer (≈5 cm) ahead of an explosively driven shock wave in noble gases is discussed and interpreted. This effect is the ionization of excited 1_u-state molecules produced due to the absorption of a small intensity flux (as compared to the ionization one) of photons (with energies substantially lower than the atom ionization threshold) by unexcited colliding complexes and van der Waals molecules. A model is proposed which explains the excitation of xenon molecules ahead of the radiationless shock wave of an open discharge. The absorption spectra of colliding complexes and van der Waals molecules adjacent to each other near the atomic absorption lines can be resolved into two spectra, and these spectra can be changed by an increase in gas temperature. As a result, radiation capable of exciting van der Waals molecules penetrates through the shock wave of an open discharge and excites xenon molecules there. The present work develops further the knowledge concerning the radiation energy transport in the shock wave front. It also proves that in front of an explosively driven shock wave a great number of excited molecules of noble gases are actually formed, and this means considerable progress toward a VUV laser with optical pumping. Translated from Preprint No. 56 of the P. N. Lebedev Physical Institute, Moscow, 1993.     

Self-assembling bipyridinium multilayers

The identification of strategies to assemble nanostructured films with engineered properties on solid supports can lead to the development of innovative functional materials. In particular, the self-assembly of electroactive multilayers from simple molecular building blocks on metallic electrodes can offer the opportunity to regulate the exchange of electrons between the underlying substrate and solution species. In this context, we designed an experimental protocol to prepare electroactive films from bipyridinium bisthiols. Specifically, we found that a compound incorporating two bipyridinium dications at its core and terminal thiol groups self-assembles into remarkably stable multilayers on polycrystalline gold. The surface coverage of the resulting films can be regulated by adjusting the exposure time of the gold substrate to the bipyridinium solution. Control experiments with appropriate model compounds demonstrate that both bipyridinium dications as well as both thiol groups must be present in the molecular skeleton to encourage multilayer growth. The resulting films transport electrons efficiently from the electrode surface to the film/solution interface. Indeed, they mediate the reduction of Ru(NH(3))(6)(3+) in the electrolyte solution but prevent the back oxidation of the resulting Ru(NH(3))(6)(2+). Furthermore, these polycationic bipyridinium films capture electrostatically Fe(CN)(6)(4-) tetraanions, which can also be exploited to transport electrons across the interfacial assembly. In fact, electrons can travel through the bipyridnium(2+/1+) couples to redox probes in solution and then back to the electrode through the Fe(CN)(6)(4/3-) couples. Thus, our original approach to self-assembling multilayers can produce stable electroactive films with unique electron transport properties, which can be regulated with a careful choice of the anionic components.     

Observation of individual particles and Coulombic solids in amicrodischarge

Spherical particles ~10-35 μm in diameter are intentionally introduced into a cylindrical microdischarge device fabricated in Al or Si. Having a diameter of 400 μm, this device is viewed along its axis with a microscope and charge-coupled device camera. Individual particles suspended in discharges in Ne are readily observable and form stable spatial patterns (in the plane transverse to the microdischarge axis) determined by the interplay of electrostatic and ion drag forces. Microdischarges may well provide an ideal testbed for exploring the application of well-characterized particles as in situ probes of plasmas     

Label-free quantitation: A new glycoproteomics approach

We demonstrate herein a method for quantifying glycosylation changes on glycoproteins. This novel method uses MS data of characterized glycopeptides to analyze glycosylation profiles, and several quality control tests were done to demonstrate that the method is reproducible, robust, applicable to different types of glycoproteins, and tolerant of instrumental variability during ionization of the analytes. This method is unique in that it is the first label-free quantitative method specifically designed for glycopeptide analysis. It can be used to monitor changes in glycosylation in a glycosylation site-specific manner on a single glycoprotein, or it can be used to quantify glycosylation in a glycoprotein mixture. During mixture analysis, the method can discriminate between changes in glycosylation of a given protein, and changes in the glycoprotein’s concentration in the mixture. This method is useful for quantitative analyses in biochemical studies of glycoproteins, where changes in glycosylation composition can be linked to functional differences; it could also be implemented in the pharmaceutical industry, where glycosylation profiles of glycoprotein-based therapeutics must be quantified. Finally, quantification of glycopeptides is an important aspect of glycopeptide-based biomarker discovery, and our quantitative approach could be a valuable asset to this field as well, provided the compositions of the glycopeptides to be quantified are identifiable using other methods.