In this study, the problem of sparse enrollment data for in-set versus out-of-set speaker recognition is addressed. The challenge here is that both the training speaker data (5 s) and test material (2~6 s) is of limited test duration. The limited enrollment data result in a sparse acoustic model space for the desired speaker model. The focus of this study is on filling these acoustic holes by harvesting neighbor speaker information to leverage overall system performance. Acoustically similar speakers are selected from a separate available corpus via three different methods for speaker similarity measurement. The selected data from these similar acoustic speakers are exploited to fill the lack of phone coverage caused by the original sparse enrollment data. The proposed speaker modeling process mimics the naturally distributed acoustic space for conversational speech. The Gaussian mixture model (GMM) tagging process allows simulated natural conversation speech to be included for in-set speaker modeling, which maintains the original system requirement of text independent speaker recognition. A human listener evaluation is also performed to compare machine versus human speaker recognition performance, with machine performance of 95% compared to 72.2% accuracy for human in-set/out-of-set performance. Results show that for extreme sparse train/reference audio streams, human speaker recognition is not nearly as reliable as machine based speaker recognition. The proposed acoustic hole filling solution (MRNC) produces an averaging 7.42% relative improvement over a GMM-Cohort UBM baseline and a 19% relative improvement over the Eigenvoice baseline using the FISHER corpus. 相似文献
The possibility that nonsupersymmetric conformal field theories softly broken below 100 TeV may provide an alternative to conventional grand unification is explored. We consider a low energy theory presumed to be of this type arising from the type IIB superstring compactified on a AdS5×S5/Γ space whose gauge group and the particle content are severely restricted by the compactification process. We present an example of a resulting SU(4)C×SU(2)L×SU(2)R with three generations, which leads to coupling unification and a prediction for sin2θW0.227 and other phenomenology generally consistent with observations. 相似文献
Inclusion studies for metal-organic open-frameworks, [Ni(C10}H24N4)(H2O)2]3[BTC]2·24H2O (1) and [Ni(C10H26N6)]3 [BTC]2·18H2O(2) (BTC3- = 1,3,5-benzenetricarboxylate) with various organic andinorganic guest molecules have been carried out. 1 is the previously reportedmolecular floral lace with 1-D channels, where positively charged macrocyclic layersand negatively charged BTC3- layers are alternately packed by hydrogen bondinginteractions. 2 is assembled in this study from nickel(II) hexaazamacrocyclic complexcontaining methyl pendant arms and BTC3-. The X-ray structure of 2 shows thatthe nickel(II) complex and BTC3- form a 2-D coordination polymer. The XRPD patternsof 2 indicate that framework of 2 is slightly deformed upon removal of waterguest molecules but restored upon rebinding of water. The host solid 1 binds MeOHin toluene, and 1,3,5-trihydroxybenzene (THB) and 4-hydroxyacetophenone (HAP) in EtOH/toluene (v/v = 1/4) solutions. The binding constants (Kf) of 1 forMeOH, THB, and HAP are 66.4 M-1, 259 M-1, and 13.9 M-1,respectively. In the range of high concentration of the guest, however, the host showsvarious binding curves depending upon the types of guest. It binds PhOH in toluene,showing a sigmoid curve. It also binds transition metal complexes such as[Cu(NH3)4](ClO4)2, [Cu(ethylenediamine)2](ClO4)2,[Cu(histamine)2](ClO4)2, and[Cu(N,N'-bis(3-aminopropyl)ethylenediamine)](ClO4)2 in MeCN, with Kf values of 645 M-1, 9.52 M-1, 37.2 M-1, and 6.00 M-1,respectively. The host solid 2 binds selectively PhOH over PhCl and PhBr, showing that hydrogen bonding interaction between the host and guest plays an important role in the selectivity. 相似文献
The title compound, C14H16N4O8S4, has crystallographic C2 symmetry with half a molecule in the asymmetric unit and a dihedral angle of 58.7 (1)° between the two planar 1,3,4‐thiadiazole five‐membered rings of the macrocyclic, giving the molecule a twisted conformation. 相似文献
In the title compound, C29H30N6, the naphthyridine ring is almost planar with a dihedral angle of 5.4 (1)° between the pyridyl rings. The dihedral angles between the naphthyridine system and the diethylaminophenyl, phenyl and pyrrolidine rings are 53.1 (1), 19.8 (1) and 20.9 (1)°, respectively. The pyrrolidine ring adopts a half‐chair conformation. The molecule is stabilized by weak C—H?N interactions. 相似文献
We construct torus bundles over locally symmetric varieties associated to cocycles in the cohomology group , where Γ is a discrete subgroup of a semisimple Lie group and L is a lattice in a real vector space. We prove that such a torus bundle has a canonical complex structure and that the space
of holomorphic forms of the highest degree on a fiber product of such bundles is isomorphic to the space of mixed automorphic
forms of a certain type.
(Received 4 September 1998) 相似文献
Summary: This communication describes an enzyme stabilization method that allows the use of enzymes irrespective of environmental factors, especially heat, while maintaining their activity for a long time. We have designed enzyme microcapsules that consist of papain enzyme cores, poly(propylene glycol) interlayers, and poly(ε‐caprolactone) walls. By confocal laser scanning microscopy measurements and the thermal stability of papain‐loaded microcapsules, it is demonstrated that the papain is surrounded by a hydrophobic polyol layer and stabilized by the exclusive volume effect. In our study, improved thermal stability can be obtained by using more hydrophobic long‐chained polyols, which is understood to be attributed to the effective formation of a hydrophobic polyol layer between the papain and the polymer wall by means of conformational anchoring in the interface.
(A) A CLSM image of a PCL microcapsule containing FITC‐labeled papain and RBITC‐labeled PPG at the same time. (B) A scheme of the role of hydrophobic polyols in the interface of enzyme and polymer. 相似文献
High-quality biocompatible magnetic iron oxide (Fe3O4) nanocrystals were developed through a ligand exchange process of hydrophobically capped nanocrystals with hydrophilic molecules. By simple modulation of the nanocrystal surface ligand charge properties, we have been able to prepare magnetic nanocrystals with excellent intracellular labeling capabilities that efficiently label a variety of cell types without the need for additional transport facilitating agents. The excellent intracellular labeling capability of the newly developed cationic WSIO has further led to successful MRI monitoring of the migration of neural stem cells in rat spinal cord. The magnetic nanocrystals developed here have great potential in applications for labeling of various cell types and also the monitoring of cell-based medical treatments and cancer metastasis. 相似文献
A 3D porous metal-organic framework [Zn3(ntb)2(EtOH)2]n.4nEtOH (1) that generates 1D channels of honeycomb aperture has been prepared by the solvothermal reaction of Zn(NO3)(2).6 H2O and 4,4',4'-nitrilotrisbenzoic acid (H3NTB) in EtOH at 110 degrees C. Framework 1 exhibits reversible single-crystal-to-single-crystal transformations upon removal and rebinding of the coordinating EtOH as well as the EtOH guest molecules, which give rise to desolvated crystal [Zn3(ntb)2]n (1') and resolvated crystal [Zn3(ntb)2-(EtOH)2]n.4nEtOH (1'). The X-ray structures indicate that 3D host framework is retained during the transformations from 1 to 1' and from 1' to 1', but the coordination geometry of ZnII ions changes from/to trigonal bipyramid to/from tetrahedron, concomitant with the rotational rearrangement of a carboxylate plane of the NTB3- relative to its associated phenyl ring. To retain the single crystal integrity, extensive cooperative motions must exist between the molecular components throughout the crystal. Framework 1' exhibits permanent porosity, thermal stability up to 400 degrees C, and blue luminescence, and high storage capabilities for N2, H2, CO2, and CH4. 相似文献
Two isomorphous 3D metal-organic frameworks, {[Cu2(BPnDC)2(bpy)].8 DMF.6 H2O}n (1) and {[Zn2(BPnDC)2(dabco)].13 DMF.3 H2O}n (2), have been prepared by the solvothermal reactions of benzophenone 4,4'-dicarboxylic acid (H2BPnDC) with Cu(NO3)(2).2.5 H2O and 4,4'-bipyridine (bpy), and with Zn(NO3)(2).6 H2O and 4-diazabicyclo[2.2.2]octane (dabco), respectively. Compounds 1 and 2 are composed of paddle-wheel {M2(O2CR)4} cluster units, and they generate 2D channels with two different large pores (effective size of larger pore: 18.2 A for 1, 11.4 A for 2). The framework structure of desolvated solid, [Cu2(BPnDC)2(bpy)]n (SNU-6; SNU=Seoul National University), is the same as that of 1, as evidenced by powder X-ray diffraction patterns. SNU-6 exhibits high permanent porosity (1.05 cm3 g(-1)) with high Langmuir surface area (2910 m2 g(-1)). It shows high H2 gas storage capacity (1.68 wt % at 77 K and 1 atm; 4.87 wt % (excess) and 10.0 wt % (total) at 77 K and 70 bar) with high isosteric heat (7.74 kJ mol(-1)) of H2 adsorption as well as high CO2 adsorption capability (113.8 wt % at 195 K and 1 atm). Compound 2 undergoes a single-crystal-to-single-crystal transformation on guest exchange with n-hexane to provide {[Zn2(BPnDC)2(dabco)].6 (n-hexane).3 H2O}n (2hexane). The transformation involves dynamic motion of the molecular components in the crystal, mainly a bending motion of the square planes of the paddle-wheel units resulting from rotational rearrangement of phenyl rings and carboxylate planes of BPnDC2-. 相似文献