The vibrational velocity, sound pressure, and acoustic power on the vibrating boundary comprising an enclosed space are reconstructed by the boundary element method based on the measured field pressures. The singular value decomposition is used to obtain the inverse solution in the least-square sense and to express the acoustic modal expansion between the measurement and source fields. In general, such an inverse operation has been considered an ill-posed problem having a divergence phenomenon involved with extremely small measurement errors. The ill-conditioned nature of the acoustic inverse problem is caused by the singularity of the transfer matrix which produces nonradiating wave components. In order to minimize the singularity and to also reduce the number of measurement points, optimal measurement positions are determined by the effective independence method. Regularization methods are used to stabilize the reconstructed field by suppressing nonradiating components resulting in the singular transfer matrix. In order to enhance the resolution of the reconstructed field, the optimal regularization order for yielding the minimum mean-square error is estimated from the known measurement noise variance by virtue of the statistical analysis. A half-scaled automotive cabin is considered an example for validating and demonstrating the proposed reconstruction process. It is noted that the present method can improve the resolution of the reconstructed field; thus vibro-acoustic parameters of the vibrating boundary can be estimated in reasonably good precision.
The aim of this study is to numerically evaluate a tunneling effect in the laboratory measurement of sound transmission loss. The tunneling effect arises from the depth of an aperture in the common wall between the source and receiving rooms. Variations of the sound transmission loss with the parameters of panel location, tunnel depth, and panel size are investigated. The difference in sound transmission loss is quite evident below the coincidence frequency and it greatly depends on the panel location in the tunnel. In comparison with the transmission loss of a finite plate in an infinite rigid baffle (with no tunnel) the maximum difference occurs in the laboratory measurement when the panel is placed at the center of the tunnel, while a better estimation of true transmission loss is obtained when the panel is located at either end. The results provide an added guideline for the standard laboratory test method for sound transmission loss.
The onset of pronucleus formation and DNA synthesis in porcine oocytes following the injection of porcine or murine sperm was determined in order to obtain insights into species-specific paternal factors that contribute to fertilisation. Similar frequencies of oocytes with female pronuclei were observed after injection with porcine sperm or with murine sperm. In contrast, male pronuclei formed 8-9 h following the injection of porcine sperm, and 6-8 h following the injection of murine sperm. After pronucleus formation maternally derived microtubules were assembled and appeared to move both male and female pronuclei to the oocyte centre. A few porcine oocytes entered metaphase 22 h after the injection of murine sperm, but normal cell division was not observed. The mean time of onset of S-phase in male pronuclei was 9.7 h following porcine sperm injection and 7.4 h following mouse sperm injection. Ultrastructural observation revealed that male pronuclei derived from murine sperm in porcine oocytes are morphologically similar to normal male pronuclei in porcine zygotes. These results suggest that species-specific paternal factors influence the onset of pronucleus formation and DNA synthesis. However, normal nuclear cytoplasmic interactions were observed in porcine S-phase oocytes following murine sperm injection.
The objective of this study was to determine developmental pattern, total cell number, apoptosis and apoptosis-related gene expression in haploid and diploid embryos following parthenogenetic activation. In vitro-matured porcine oocytes were activated by electrical pulses and cultured in the absence or presence of cytochalasin B for 3 h. Zygotes with two polar bodies (haploid) and one polar body (diploid) were carefully selected and were further cultured in NCSU 23 medium containing 0.4% bovine serum albumin (BSA) for 7 days. The percentage of development to blastocyst stage was higher (p < 0.01) in the diploid than in the haploid parthenotes. In haploid blastocysts, average total cell number was significantly reduced (p < 0.05) and apoptosis was increased at day 7. The relative abundance of Bcl-xL and Bak mRNA in the diploid blastocysts was similar to that of in vivo-fertilized embryos. However, Bcl-xL was significantly decreased, and Bak mRNA was significantly increased (p < 0.05) in haploid parthenotes compared with the diploid parthenotes. These results suggest that the haploid state affects apoptosis-related gene expression which results in increased apoptosis and decreased developmental competence of haploid parthenotes.
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