Narrow band quantitative and multivariate electroencephalogram analysis of peri-adolescent period

ABSTRACT: BACKGROUND: The peri-adolescent period is a crucial developmental moment of transition from childhood to emergent adulthood. The present report analyses the differences in Power Spectrum (PS) of the Electroencephalogram (EEG) between late childhood (24 children between 8 and 13 years old) and young adulthood (24 young adults between 18 and 23 years old). RESULTS: The narrow band analysis of the Electroencephalogram was computed in the frequency range of 0--20 Hz. The analysis of mean and variance suggested that six frequency ranges presented a different rate of maturation at these ages, namely: low delta, delta-theta, low alpha, high alpha, low beta and high beta. For most of these bands the maturation seems to occur later in anterior sites than posterior sites. Correlational analysis showed a lower pattern of correlation between different frequencies in children than in young adults, suggesting a certain asynchrony in the maturation of different rhythms. The topographical analysis revealed similar topographies of the different rhythms in children and young adults. Principal Component Analysis (PCA) demonstrated the same internal structure for the Electroencephalogram of both age groups. Principal Component Analysis allowed to separate four subcomponents in the alpha range. All these subcomponents peaked at a lower frequency in children than in young adults. CONCLUSIONS: The present approaches complement and solve some of the incertitudes when the classical brain broad rhythm analysis is applied. Children have a higher absolute power than young adults for frequency ranges between 0-20 Hz, the correlation of Power Spectrum (PS) with age and the variance age comparison showed that there are six ranges of frequencies that can distinguish the level of EEG maturation in children and adults. The establishment of maturational order of different frequencies and its possible maturational interdependence would require a complete series including all the different ages.     

Transfer measurements for the Ti+Ni systems at near barrier energies

Large enhancements have been observed in the sub-barrier fusion cross sections for Ti+Ni systems in our previous studies. Coupled channel calculations incorporating couplings to 2⁺ and 3⁻ states failed to explain these enhancements completely. A possibilty of transfer channels contributing to the residual enhancements had been suggested. In order to investigate the role of relevant transfer channels, measurements of one- and two-nucleon transfer were carried out for ^46,48Ti+⁶¹Ni systems. The present paper gives the results of these studies.     

Selective organic functionalization of polycrystalline silicon-germanium for bioMEMS applications

We selectively immobilized organofunctional silanes on top of polycrystalline silicon-germanium (poly-SiGe) layers, as a first step towards the fabrication of poly-SiGe-based bioMEMS (biomedical MicroElectroMechanicalSystems) by means of standard UV photolithography. 3-aminopropyl-dimethyl-ethoxysilane (APDMES) and 3-aminopropyl-triethoxysilane (APTES) molecules were immobilized onto resist-patterned poly-SiGe surfaces. The protocols for surface hydroxylation and silane immobilization were designed to be CMOS-compatible and to avoid damage to photoresist. Silanized surfaces were investigated both by means of fluorescence microscopy, and by FEG-SEM observation after labeling with 30 nm-diameter gold nanoparticles (NPs). We report the silanization protocols, together with the results indicating successful organic functionalization of the samples.     

(Z)-3-p-tolylsulfinylacrylonitrile as a chiral dienophile: diels-alder reactions with furan and acyclic dienes

The behavior of (Z)-3-p-tolylsulfinylacrylonitrile (1) as a chiral dienophile has been evaluated from its reactions with furan and acyclic dienes. Electrostatic interactions of the cyano group with the sulfinyl one restrict the conformational mobility around the C-S bond, thus controlling the pi-facial selectivity, which is almost complete in all cases, the approach of the diene from the less-hindered face of the dienophile (that bearing the lone electron pair) in the predominant rotamer being the favored one. The regioselectivity is also completely controlled by the cyano group. Additionally, the reactivity of compound 1 as well as its endo-selectivity are both higher than those observed for the corresponding (Z)-3-sulfinylacrylates, thus proving the potential of sulfinylnitriles as chiral dienophiles.     

ROMPgel-supported tris(triphenylphosphine)rhodium(I) chloride: a selective hydrogenation catalyst for parallel synthesis

ROMPgel-supported tris(triphenylphosphine)rhodium(I) chloride has been prepared and the immobilised catalyst has been effectively employed in selective hydrogenations of a variety of alkenes and terminal alkynes.     

Eigenvalue Asymptotics of the Stokes Operator for Fractal Domains

The leading asymptotic term for the function that counts theeigenvalues of the Stokes operator is determined for fairlygeneral underlying bounded domains. Moreover, the remainderis estimated in terms of the fractality of the boundary of thedomain. The results obtained resemble corresponding ones forthe Dirichlet Laplacian. 1991 Mathematics Subject Classification:35P20.     

On the order of global branches

We give both a topological and an algebraic definition of the order of a global branch of a variety along a subvariety. Then we show that these two definitions agree. Finally we compare this order with the orders of the related local branches.

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Sunto Diamo due definizioni, una topologica e una algebrica, di ordine di un ramo globale di una varietà lungo una sottovarietà. Poi mostriamo che queste due definizioni coincidono. Infine confrontiamo questo ordine con gli ordini dei relativi rami locali.

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Partially supported by CNR funds.     

Permanganate oxidation of 3-methyl-4-nitro-5-styrilisoxazole: a correction

In contrast with a previous report, permanganate oxidation of the title compound $\text{3}$ gives the nitroisoxazolone $\text{8}$ and not 3-methyl-4- nitroisoxazole-5-carboxylic acid $\text{2}$; a reaction pathway, involving the spirocyclisation of the carboxylate $\text{10}$, is suggested.