Uniqueness of structures for connective covers

We refine our earlier work on the existence and uniqueness of structures on -theoretic spectra to show that the connective versions of real and complex -theory as well as the connective Adams summand at each prime have unique structures as commutative -algebras. For the -completion we show that the McClure-Staffeldt model for is equivalent as an ring spectrum to the connective cover of the periodic Adams summand . We establish a Bousfield equivalence between the connective cover of the Lubin-Tate spectrum and .

     

Perfect Baer Subplane Partitions and Three-Dimensional Flag-Transitive Planes

The classification of perfectBaer subplane partitions of PG(2, q²) is equivalentto the classification of 3-dimensional flag-transitive planeswhose translation complements contain a linear cyclic group actingregularly on the line at infinity. Since all known flag-transitiveplanes admit a translation complement containing a linear cyclicsubgroup which either acts regularly on the points of the lineat infinity or has two orbits of equal size on these points,such a classification would be a significant step towards theclassification of all 3-dimensional flag-transitive planes. Usinglinearized polynomials, a parametric enumeration of all perfectBaer subplane partitions for odd q is described.Moreover, a cyclotomic conjecture is given, verified by computerfor odd prime powers q < 200, whose truth would implythat all perfect Baer subplane partitions arise from a constructionof Kantor and hence the corresponding flag-transitive planesare all known.     

Wave reflection and transmission in beams containing delamination and inhomogeneity

This paper presents an analytical approach using higher order plate theories to determine wave reflections from and transmissions through a damaged region in a beam. The damaged region is either treated as two split beams or as an inhomogeneity. The reflection ratios and transmission ratios are found to depend strongly on the frequency of the incident flexural waves, as well as the size of the damage, which gives rise to strong stop/pass band behaviour. Using the spectral analysis method, the transient wave propagation in a beam with a part-through delamination is predicted and compared with experimental results, indicating a good agreement in the phases and amplitudes of both the reflected and transmitted waves.     

Three‐dimensional blockmodels

In the classic blockmodel formulation, a social network among members of a population with n actors and k relations (types of tie) is arrayed as k n X n matrices. Though this is a three‐dimensional data structure, it is typically reduced to a two‐way analysis. In this paper, a three‐way procedure for analyzing multigraph data is developed. Specifically, in addition to applying the rule of structural equivalence to collapse actors, it is also applied to the relations (the third dimension), and structurally equivalent sets of relations are collapsed. The result is a three‐dimensional blockmodel (image) of social structure that is a more parsimonious representation of social structure than the classic two‐dimensional blockmodel images. The three‐dimensional approach is illustrated by application to three case studies: Homan's Bank Wiring Room, Sampson's monastery, and a local economy of hospital services. The structural equivalence approach to relations is further explored by applying it to the individual‐level Liking and Antagonism relations and their compounds (of length four or less) in the Bank Wiring Room. This application demonstrates that the structural equivalence approach can be used to identify equality equations for primitive and compound relations.     

The determination of certain major and minor elements in geological samples by inductively coupled plasma atomic emission spectrometry. Some interference problems with the analysis of geological standard reference materials and nutrition supplements

Direct ICP-AES measurements of the digested geological standard reference material samples yielded the wrong information about their composition. The differences between certified and measured concentrations of the samples were due to the complicated sample matrix. The measured concentrations can be successfully corrected by using a multiple linear regression technique. The correction is based on the multiple regression line calculated from the analytical results at synthetic mixtures of matrix elements, where concentrations varied on five levels. There were no significant (P = 0.05) differences between certified and measured concentrations in standard reference materials after the correction. The same method was used in the analysis of nutrition supplements. Received: 25 January 2000 / Revised: 15 March 2000 / Accepted: 31 March 2000     

Adiabatic and nonadiabatic dynamics in the CH3(CD3)+HCl reaction

The scattering dynamics leading to the formation of Cl (2P(3/2)) and Cl* (2P(1/2)) products of the CH(3)+HCl reaction (at a mean collision energy =22.3 kcal mol(-1)) and the Cl (2P(3/2)) products of the CD(3)+HCl reaction (at =19.4 kcal mol(-1)) have been investigated by using photodissociation of CH(3)I and CD(3)I as sources of translationally hot methyl radicals and velocity map imaging of the Cl atom products. Image analysis with a Legendre moment fitting procedure demonstrates that, in all three reactions, the Cl/Cl* products are mostly forward scattered with respect to the HCl in the center-of-mass (c.m.) frame but with a backward scattered component. The distributions of the fraction of the available energy released as translation peak at f(t)=0.31-0.33 for all the reactions, with average values that lie in the range =0.42-0.47. The detailed analysis indicates the importance of collision energy in facilitating the nonadiabatic transitions that lead to Cl* production. The similarities between the c.m.-frame scattering and kinetic energy release distributions for Cl and Cl* channels suggest that the nonadiabatic transitions to a low-lying excited potential energy surface (PES) correlating to Cl* products occur after passage through the transition state region on the ground-state PES. Branching fractions for Cl* are determined to be 0.14+/-0.02 for the CH(3)+HCl reaction and 0.20+/-0.03 for the CD(3)+HCl reaction. The difference cannot be accounted for by changes in collision energy, mass effects, or vibrational excitation of the photolytically generated methyl radical reagents and instead suggests that the low-frequency bending modes of the CD(3)H or CH(4) coproduct are important mediators of the nonadiabatic couplings occurring in this reaction system.     

Deposition of DNA-functionalized gold nanospheres into nanoporous surfaces

We report the deposition of DNA-conjugated gold nanospheres into arrays of surface nanopores obtained from hexagonally ordered thin polystyrene-b-poly(methyl methacrylate) (PS-b-PMMA) diblock copolymer films on silicon. The deposition occurs spontaneously from aqueous solution and is driven by either electrostatic interactions or specific DNA hybridization events between the DNA nanospheres and the surface nanopores. To mitigate this spontaneous deposition, we have chemically modified the nanopores with either positively charged aminosilanes or oligonucleotide probe sequences. The deposition of DNA nanospheres into the surface nanopores was characterized by atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). We have observed preferential immobilization of individual DNA nanospheres within the nanopores, based on the size matching between the two entities. The inclusion density and selectivity of DNA nanosphere deposition into the surface nanopores was found to depend predominantly on the methods through which the nanoporous surfaces were prepared and chemically functionalized.