Comodulation masking release in consonant recognition

Comodulation masking release (CMR) refers to an improvement in the detection threshold of a signal masked by noise with coherent amplitude fluctuation across frequency, as compared to noise without the envelope coherence. The present study tested whether such an advantage for signal detection would facilitate the identification of speech phonemes. Consonant identification of bandpass speech was measured under the following three masker conditions: (1) a single band of noise in the speech band ("on-frequency" masker); (2) two bands of noise, one in the on-frequency band and the other in the "flanking band," with coherence of temporal envelope fluctuation between the two bands (comodulation); and (3) two bands of noise (on-frequency band and flanking band), without the coherence of the envelopes (noncomodulation). A pilot experiment with a small number of consonant tokens was followed by the main experiment with 12 consonants and the following masking conditions: three frequency locations of the flanking band and two masker levels. Results showed that in all conditions, the comodulation condition provided higher identification scores than the noncomodulation condition, and the difference in score was 3.5% on average. No significant difference was observed between the on-frequency only condition and the comodulation condition, i.e., an "unmasking" effect by the addition of a comodulated flaking band was not observed. The positive effect of CMR on consonant recognition found in the present study endorses a "cued-listening" theory, rather than an envelope correlation theory, as a basis of CMR in a suprathreshold task.     

Study of alkyl chain length dependent characteristics of imidazolium based ionic liquids [CnMIM]+[TFSA]− by Brillouin and dielectric loss spectroscopy

This study examined the acoustic phonon mode of ionic liquids consisting of 1-alkyl-3-methyl-imidazolium family (C_nMIM) cations with n values ranging from 2 to 10 and bis(trifluoromethylsulfonyl)amide (TFSA) anion in the temperature range from 300 K to 100 K. [C_nMIM]⁺[TFSA]^? showed depolarized (VH) components of Brillouin peaks at temperatures below the glass transition temperature when n is larger than 4. On the other hand, in the case of ionic liquids with different anions, such as [C₄MIM]⁺[BF₄]^?, [C₄MIM]⁺[PF₆]^? and [C₈MIM]⁺[BF₄]^?, the VH component of Brillouin peaks was not observed in the temperature range investigated. The dielectric loss spectra showed that the temperature dependence of alkyl chain domain relaxation of all ionic liquids followed the Arrhenius law and showed an increase in activation energy at the temperature where the VH component of Brillouin peak appeared. These results suggest that the observed depolarized component of Brillouin peak might originate from uniquely induced polarization in the 2nd domain composed of head groups of cations and anions.     

On Kernel polynomials and self-perturbation of orthogonal polynomials

Given an orthogonal polynomial system {Q _n (x)} _n=0 ^∞, define another polynomial system by where α _n are complex numbers and t is a positive integer. We find conditions for {P _n (x)} _n=0 ^∞ to be an orthogonal polynomial system. When t=1 and α₁≠0, it turns out that {Q _n (x)} _n=0 ^∞ must be kernel polynomials for {P _n (x)} _n=0 ^∞ for which we study, in detail, the location of zeros and semi-classical character. Received: November 25, 1999; in final form: April 6, 2000?Published online: June 22, 2001     

Hyperbolic mean growth of bounded holomorphic functions in the ball

We consider the hyperbolic Hardy class , . It consists of holomorphic in the unit complex ball for which and

where denotes the hyperbolic distance of the unit disc. The hyperbolic version of the Littlewood-Paley type -function and the area function are defined in terms of the invariant gradient of , and membership of is expressed by the property of the functions. As an application, we can characterize the boundedness and the compactness of the composition operator , defined by , from the Bloch space into the Hardy space .

     

Hyperfunctional Weights for Orthogonal Polynomials

The Chebychev polynomials associated to any given moments μ_{n ∞} ⁰ are formally orthogonal with respect to the formal δ-series $$w(x)= {\sum^\infty_0}(- 1)^{n}\mu_{{n}}\delta^{(n)}(x)/n!.$$ We show that this formal weight can be a true hyperfunctional weight if its Fourier transform is a slowly increasing holomorphic function in some tubular neighborhood of the real line. It provides a unifying treatment of real and complex orthogonality of Chebychev polynomials including all classical examples and characterizes Chebychev polynomials having Bessel type orthogonality.     

Observation of B(s)(0) → D(s)(*)+ D(s)(*)- using e+ e- collisions and a determination of the B(s)-B(s) width difference ΔΓ(s)

We have made the first observation of B(s)(0)→D(s)(*)+ D(s)(*)- decays using 23.6 fb(-1) of data recorded by the Belle experiment running on the Υ(5S) resonance. The branching fractions are measured to be B(B(s)(0)→D(s)+ D(s)-)=(1.03(-0.32-0.25)(+0.39+0.26))%, B(B(s)(0)→D(s)(*±) D(s)(?))=(2.75(-0.71)(+0.83)±0.69)%, and B(B(s)(0)→D(s)*+ D(s)*-)=(3.08(-1.04-0.86)(+1.22+0.85))%; the sum is B[B(s)(0)→D(s)(*)+ D(s)(*)-]=(6.85(-1.30-1.80)(+1.53+1.79))%. Assuming B(s)(0)→D(s)(*)+ D(s)(*)- saturates decays to CP-even final states, the branching fraction determines the ratio ΔΓ(s)/cosφ, where ΔΓ(s) is the difference in widths between the two B(s)-B(s) mass eigenstates, and φ is a CP-violating weak phase. Taking CP violation to be negligibly small, we obtain ΔΓ(s)/Γ(s)=0.147(-0.030)(+0.036)(stat)(-0.041)(+0.042)(syst), where Γ(s) is the mean decay width.     

Preparation and characterization of carbamoylphosphonate(CMPO) silane grafted on various mesoporous silicas

The carbamoylphosphosphonate silane (CMPO analogue; 2-(diphenylphosphoryl)-N-(3-(triethoxysilyl)propyl) acetamide) modified mesoporous silica was prepared via a post-synthesis grafting method for the effective purification of rare earth elements. The guest CMPO analogue was synthesized by direct coupling reaction of 2-(diphenylphosphoryl) acetic acid and 3-(triethoxysilyl)propan-1-amine. Various mesoporous silicates such as MCM-41, SBA-15, or amorphous silica nanoparticles were adopted as host materials. The resulting surface-modified mesoporous materials were characterized with respect to their structural integrity, surface area, and pore size and the concentration of the CMPO silane species. These CMPO functionalized periodic mesostructured silicates offer the potential of applications as catalysts, sensors, or environmental sorbents.     

Dynamics of macroautophagy: Modeling and oscillatory behavior

We propose a model for macroautophagy and study the resulting dynamics of autophagy in a system isolated from its extra-cellular environment. It is found that the intracellular concentrations of autophagosomes and autolysosomes display oscillations with their own natural frequencies. Such oscillatory behaviors, which are interrelated to the dynamics of intracellular ATP, amino acids, and proteins, are consistent with the very recent biological observations. Implications of this theoretical study of autophagy are discussed, with regard to the possibility of guiding molecular studies of autophagy.     

A branch and bound algorithm for disassembly scheduling with assembly product structure

This paper considers a production planning problem in disassembly systems, which is the problem of determining the quantity and timing of disassembling end-of-use/life products in order to satisfy the demand of their parts or components over a planning horizon. The case of single product type without parts commonality is considered for the objective of minimizing the sum of setup and inventory holding costs. To show the complexity of the problem, we prove that the problem is NP-hard. Then, after deriving the properties of optimal solutions, a branch and bound algorithm is suggested that incorporates the Lagrangean relaxation-based upper and lower bounds. Computational experiments are performed on a number of randomly generated problems and the test results indicate that the branch and bound algorithm can give optimal solutions up to moderate-sized problems in a reasonable computation time. A Lagrangean heuristic for a viable alternative for large-sized problems is also suggested and compared with the existing heuristics to show its effectiveness.     

MAO‐free and extremely active catalytic system for ethylene tetramerization

The original Sasol catalytic system for ethylene tetramerization is composed of a Cr source, a PNP ligand, and MAO (methylaluminoxane). The use of expensive MAO in excess has been a critical concern in commercial operation. Many efforts have been made to replace MAO with non‐coordinating anions (e.g., [B(C₆F₅)₄]^?); however, most of such attempts were unsuccessful. Herein, an extremely active catalytic system that avoids the use of MAO is presented. The successive addition of two equivalent [H(OEt₂)₂]⁺[B(C₆F₅)₄]^? and one equivalent CrCl₃(THF)₃ to (acac)AlEt₂ and subsequent treatment with a PNP ligand [CH₃(CH₂)₁₆]₂C(H)N(PPh₂)₂ ( 1 ) yielded a complex presumably formulated as [ 1 ‐CrAl (acac)Cl₃(THF)]²⁺[B(C₆F₅)₄]^?₂, which exhibited high activity when combined with iBu₃Al (1120 kg/g‐Cr/h; ~4 times that of the original Sasol system composed of Cr (acac)₃, iPrN(PPh₂)₂, and MAO). Via the introduction of bulky trialkylsilyl substituents such as –SiMe₃, –Si(nBu)₃, or –SiMe₂(CH₂)₇CH₃ at the para‐position of phenyl groups in 1 (i.e., by using [CH₃(CH₂)₁₆]₂C(H)N[P(C₆H₄‐p‐SiR₃)₂]₂ instead of 1 ), the activities were dramatically improved, i.e., tripled (2960–3340 kg/g‐Cr/h; more than 10 times that of the original Sasol system). The generation of significantly less PE (<0.2 wt%) even at a high temperature is another advantage achieved by the introduction of bulky trialkylsilyl substituents. NMR studies and DFT calculations suggest that increase of the steric bulkiness on the alkyl‐N and P‐aryl moieties restrict the free rotation around (alkyl)N–P (aryl) bonds, which may cause the generation of more robust active species in higher proportion, leading to extremely high activity along with the generation of a smaller amount of PE.