Thermodynamic database of the phase diagrams in copper base alloy systems

通讯作者地址: Ishida, K (通讯作者), Tohoku Univ, Grad Sch Engn, Dept Mat Sci, Aoba Yama 02, Sendai, Miyagi 9808579 Japan 地址: 1. Tohoku Univ, Grad Sch Engn, Dept Mat Sci, Sendai, Miyagi 9808579 Japan 2. Xiamen Univ, Dept Mat Sci & Engn, Xiamen 361005, Peoples R China 电子邮件地址: [email protected] thermodynamic database on the phase equilibria of the copper base alloys, including Cu-X binary system and Cu-Fe, Cu-Ni, Cu-Cr base ternary systems has been developed by the Calculation of Phase Diagrams (CALPHAD) method. The thermodynamic parameters describing Gibbs energies of the different phases have been evaluated by optimizing experimental data of phase equilibria and thermodynamic properties. The present thermodynamic database can provide much information such as stable and metastable phase equilibria, phase fraction, liquidus projection and various thermodynamic quantities and so on, which is expected to play an important role in the design of copper base alloys. (c) 2004 Elsevier Ltd. All rights reserved

Thermodynamic assessments of the Cu-Mn-X (X : Fe, Co) systems

通讯作者地址: Liu, XJ (通讯作者), Xiamen Univ, Coll Chem & Chem Engn, Dept Mat Sci & Engn, Xiamen 361005, Peoples R China 地址: 1. Xiamen Univ, Coll Chem & Chem Engn, Dept Mat Sci & Engn, Xiamen 361005, Peoples R China 2. Tohoku Univ, Grad Sch Engn, Dept Mat Sci, Sendai, Miyagi 9808579 Japan 电子邮件地址: [email protected] thermodynamic assessments of the Cu-Mn binary, Cu-Mn-Fe and Cu-Mn-Co ternary systems were carried out by using CALPHAD (calculation of phase diagrams) method on the basis of the experimental data including the thermodynamic properties and phase equilibria. The Gibbs free energies of the liquid, bcc, fcc, hep, (alpha Mn) and (beta Mn) phases are described by the subregular solution model. The thermodynamic parameters of the Cu-Mn binary, Cu-Mn-Fe and Cu-Mn-Co ternary systems have been optimized for reproducing the experimental results in each system, respectively. An agreement between the calculated results and experimental data is obtained. (C) 2006 Published by Elsevier B.V

Thermodynamic calculation of phase equilibria in the Cu-Ni-Zn system

通讯作者地址: Jiang, M (通讯作者), Tohoku Univ, Grad Sch Engn, Dept Mat Sci, Sendai, Miyagi 9808579 Japan 地址: 1. Tohoku Univ, Grad Sch Engn, Dept Mat Sci, Sendai, Miyagi 9808579 Japan 2. Xiamen Univ, Dept Mat Sci & Engn, Xiamen 361005, Peoples R China 3. Univ Sofia, Fac Chem, Sofia 1164, Bulgaria 电子邮件地址: [email protected] ternary system of Cu-Ni-Zn has been thermodynamically analyzed based on extensive experimental information and reasonable thermodynamic modeling work by using the CALPHAD approach. A self-consistent set of thermodynamic parameters has been obtained, and the experimentally determined phase equilibria in the whole composition range except for the Zn-rich portion have been critically reproduced. The thermodynamic description established in this work can be used in predicting the phase relationships and thermodynamic properties in the Cu-Ni-Zn system. (c) 2004 Elsevier Ltd. All rights reserved

Gibbs energies of reaction and microbial mutualism in anaerobic deep subseafloor sediments of ODP Site 1226

In situ Gibbs energies of reaction (AG) for acetate-oxidizing sulfate reduction, acetate-oxidizing iron reduction, and acetoclastic methanogenesis, and sulfate-reducing methanotrophy are consistently negative and relatively constant throughout most of the sediment column at the eastern equatorial Pacific Ocean Drilling Program (ODP) Site 1226. The energy yields (-Delta G) closely match the values (for acetate-oxidizing sulfate reduction and acetoclastic methanogenesis) in published culturing experiments with actively growing cells and, for sulfate-reducing methanotrophy, in other environments. Although microbes mediating these reactions compete for substrates, mutualistic interactions between them appear to sustain their co-existence in deep subseafloor sediments for millions of years (the interval over which the sediments have been deposited). These competing and mutualistic interactions collectively constitute a highly coupled reaction network where relative rates of reaction are regulated by the in situ Gibbs energies of reaction. (C) 2010 Elsevier Ltd. All rights reserved.NASA Astrobiology Institut

FOOTSTEP DETECTION AND CLASSIFICATION USING DISTRIBUTED MICROPHONES

ABSTRACT This paper addresses footstep detection and classification with multiple microphones distributed on the floor. We propose to introduce geometrical features such as position and velocity of a sound source for classification which is estimated by amplitude-based localization. It does not require precise inter-microphone time synchronization unlike a conventional microphone array technique. To classify various types of sound events, we introduce four types of features, i.e., time-domain, spectral and Cepstral features in addition to the geometrical features. We constructed a prototype system for footstep detection and classification based on the proposed ideas with eight microphones aligned in a 2-by-4 grid manner. Preliminary classification experiments showed that classification accuracy for four types of sound sources such as a walking footstep, running footstep, handclap, and utterance maintains over 70% even when the signal-to-noise ratio is low, like 0 dB. We also confirmed two advantages with the proposed footstep detection and classification. One is that the proposed features can be applied to classification of other sound sources besides footsteps. The other is that the use of a multichannel approach further improves noise-robustness by selecting the best microphone among the microphones, and providing geometrical information on a sound source

Ardisinones A-E, novel diarylundecanones from Ardisia arborescens

A phytochemical study on an ethanol extract of Ardisia arborescens resulted in the isolation of five new diarylundecanones, named ardisinones A-E (1-5). The structures were established by HRESIMS and NMR (H-1, C-13, DEPT, HSQC, HMBC) as 11-(2-acetoxy-6-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)undecan-1-one (1), 11-(2-acetoxy-6-hydroxyphenyl)-1-(2,6-dihydroxy-4-methoxyphenyl)undecan- 1-one (2), 1-(2,6-dihydroxy-4-methoxyphenyl)-11-(2,6-dihydroxyphenyl)undecan-1-one (3), 1-(2,4,6-trihydroxyphenyl)-11-(2,6-dihydroxyphenyl)undecan-1-one (4), and 1-(2,4,6-trihydroxyphenyl)-11-(2-hydroxyphenyl)undecan-1-one (5). In our in vitro disk diffusion assay, compounds 1 and 4 showed some slight inhibition of three bacteria, while 2 and 3 did not show antimicrobial activity

Clonal diversity and genealogical relationships of gibel carp in four hatcheries

To conserve and utilize the genetic pool of gynogenetic gibel carp (Carassius auratus gibelio), the Fangzheng and Qihe stock hatcheries have been established in China. However, little information is available on the amount of genetic variation within and between these populations. In this study, clonal diversity in 101 fish from these two stock hatcheries and 35 fish from two other hatcheries in Wuhan and Pengze respectively was analysed for variation in serum transferrin. Thirteen clones were found in Fangzheng and Qihe, of which 12 were novel. Six clones were specific to Fangzheng and three specific to Qihe, whereas four were shared among the Fangzheng and Qihe fish. To obtain more knowledge on genetic diversity and genealogical relationships within gibel carp, the complete mitochondrial DNA (mtDNA) control region (similar to 920 bp) was sequenced in 64 individuals representing all 14 clones identified in the four hatcheries. Differences in the mtDNA sequences varied remarkably among hatcheries, with the Fangzheng and Qihe lines demonstrating high diversity and Wuhan and Pengze showing no variation. The Fangzheng and Qihe lines might represent two distinct matrilineal sources. One of the Qihe samples carried the haplotype shared by a most widely cultivated Fangzheng clone, indicating that a Fangzheng clone escaped from cultivated ponds and moved into the Qihe hatchery. Four Fangzheng samples clustered within the lineage formed mainly by Qihe samples, most likely reflecting historical gene flow from Qihe to Fangzheng. It is suggested that clones in Wuhan originated from Fangzheng, consistent with their introduction history, supporting the hypothesis that gibel carp in Pengze were domesticated from individuals in the Fangzheng hatchery.To conserve and utilize the genetic pool of gynogenetic gibel carp (Carassius auratus gibelio), the Fangzheng and Qihe stock hatcheries have been established in China. However, little information is available on the amount of genetic variation within and between these populations. In this study, clonal diversity in 101 fish from these two stock hatcheries and 35 fish from two other hatcheries in Wuhan and Pengze respectively was analysed for variation in serum transferrin. Thirteen clones were found in Fangzheng and Qihe, of which 12 were novel. Six clones were specific to Fangzheng and three specific to Qihe, whereas four were shared among the Fangzheng and Qihe fish. To obtain more knowledge on genetic diversity and genealogical relationships within gibel carp, the complete mitochondrial DNA (mtDNA) control region (similar to 920 bp) was sequenced in 64 individuals representing all 14 clones identified in the four hatcheries. Differences in the mtDNA sequences varied remarkably among hatcheries, with the Fangzheng and Qihe lines demonstrating high diversity and Wuhan and Pengze showing no variation. The Fangzheng and Qihe lines might represent two distinct matrilineal sources. One of the Qihe samples carried the haplotype shared by a most widely cultivated Fangzheng clone, indicating that a Fangzheng clone escaped from cultivated ponds and moved into the Qihe hatchery. Four Fangzheng samples clustered within the lineage formed mainly by Qihe samples, most likely reflecting historical gene flow from Qihe to Fangzheng. It is suggested that clones in Wuhan originated from Fangzheng, consistent with their introduction history, supporting the hypothesis that gibel carp in Pengze were domesticated from individuals in the Fangzheng hatchery

Ectopic Six3 expression in the dragon eye goldfish

For goldfish (Carassius auratus), there are many varieties with different eye phenotypes due to artificial selection and adaptive evolution. Dragon eye is a variant eye characterized by a large-size eyeball protruding out of the socket similar to the eye of dragon in Chinese legends. In this study, anatomical structure of the goldfish dragon eye was compared with that of the common eye, and a stretching of the retina was observed in the enlarged dragon eye. Moreover, the homeobox-containing transcription factor Six3 cDNAs were cloned from the two types of goldfish, and the expression patterns were analyzed in both normal eye and dragon eye goldfish. No amino acid sequence differences were observed between the two deduced peptides, and the expression pattern of Six3 protein in dragon eye is quite similar to common eye during embryogenesis, but from 2 days after hatching, ectopic Six3 expression began to occur in the dragon eye, especially in the outer nuclear layer cells. With eye development, more predominant Six3 distribution was detected in the outer nuclear layer cells of dragon eye than that of normal eye, and fewer cell-layers in outer nuclear layer were observed in dragon eye retina than in normal eye retina. The highlight of this study is that higher Six3 expression occurs in dragon eye goldfish than in normal eye goldfish during retinal development of larvae. (C) 2007 Elsevier Inc. All rights reserved.For goldfish (Carassius auratus), there are many varieties with different eye phenotypes due to artificial selection and adaptive evolution. Dragon eye is a variant eye characterized by a large-size eyeball protruding out of the socket similar to the eye of dragon in Chinese legends. In this study, anatomical structure of the goldfish dragon eye was compared with that of the common eye, and a stretching of the retina was observed in the enlarged dragon eye. Moreover, the homeobox-containing transcription factor Six3 cDNAs were cloned from the two types of goldfish, and the expression patterns were analyzed in both normal eye and dragon eye goldfish. No amino acid sequence differences were observed between the two deduced peptides, and the expression pattern of Six3 protein in dragon eye is quite similar to common eye during embryogenesis, but from 2 days after hatching, ectopic Six3 expression began to occur in the dragon eye, especially in the outer nuclear layer cells. With eye development, more predominant Six3 distribution was detected in the outer nuclear layer cells of dragon eye than that of normal eye, and fewer cell-layers in outer nuclear layer were observed in dragon eye retina than in normal eye retina. The highlight of this study is that higher Six3 expression occurs in dragon eye goldfish than in normal eye goldfish during retinal development of larvae. (C) 2007 Elsevier Inc. All rights reserved

Characterization and application of monoclonal antibodies against turbot (Scophthalmus maximus) rhabdovirus

Five monoclonal antibodies (mAbs), 1G8, 1H9, 2D2, 2D3, and 2F5, against Scophthalmus maximus rhabdovirus (SMRV) were prepared. Characterization of the mAbs included indirect enzyme-linked immunosorbent assay, isotyping, viral inhibition assay, immunofluorescence staining of virus-infected cell cultures, and Western blot analysis. Isotyping revealed that 1G8 and 1H9 were of the IgG2b subclass and that the other three were IgM. 2D2, 2D3, and 2F5 partially inhibited SMRV infection in epithelioma. papulosum cyprinid (EPC) cell culture. Western blotting showed that all five mAbs could react with two SMRV proteins with molecular masses of approximately 30 kDa (P) and 26 kDa (M). These two proteins were localized within the cytoplasm of SMRV-infected EPC cells by immunofluorescence assay. Also, progressive foci of viral replication in cell cultures were monitored from 6 to 24 h, using mAb 2D3 as the primary antibody. A flow cytometry procedure was used to detect and quantify SMRV-infected (0.01 PFU/cell) EPC cells with mAb 2D3, and 10.8% of cells could be distinguished as infected 36 h postinfection. Moreover, mAb 2D3 was successfully applied for the detection of viral antigen in cryosections from flounder tissues by immunohistochemistry tests.Five monoclonal antibodies (mAbs), 1G8, 1H9, 2D2, 2D3, and 2F5, against Scophthalmus maximus rhabdovirus (SMRV) were prepared. Characterization of the mAbs included indirect enzyme-linked immunosorbent assay, isotyping, viral inhibition assay, immunofluorescence staining of virus-infected cell cultures, and Western blot analysis. Isotyping revealed that 1G8 and 1H9 were of the IgG2b subclass and that the other three were IgM. 2D2, 2D3, and 2F5 partially inhibited SMRV infection in epithelioma. papulosum cyprinid (EPC) cell culture. Western blotting showed that all five mAbs could react with two SMRV proteins with molecular masses of approximately 30 kDa (P) and 26 kDa (M). These two proteins were localized within the cytoplasm of SMRV-infected EPC cells by immunofluorescence assay. Also, progressive foci of viral replication in cell cultures were monitored from 6 to 24 h, using mAb 2D3 as the primary antibody. A flow cytometry procedure was used to detect and quantify SMRV-infected (0.01 PFU/cell) EPC cells with mAb 2D3, and 10.8% of cells could be distinguished as infected 36 h postinfection. Moreover, mAb 2D3 was successfully applied for the detection of viral antigen in cryosections from flounder tissues by immunohistochemistry tests

Mtmr8 is essential for vasculature development in zebrafish embryos

Background: Embryonic morphogenesis of vascular and muscular systems is tightly coordinated, and a functional cooperation of Mtmr8 with PI3K in actin filament modeling and muscle development has been revealed in zebrafish. Here, we attempt to explore the function of Mtmr8 in vasculature development parallel to its function in muscle development. Results: During early stage of somitogenesis, mtmr8 expression was detected in both somitic mesodem and ventral mesoderm. Knockdown of mtmr8 by morpholino impairs arterial endothelial marker expression, and results in endothelial cell reduction and vasculogenesis defects, such as retardation in intersegmental vessel development and interruption of trunk dorsal aorta. Moreover, mtmr8 morphants show loss of arterial endothelial cell identity in dorsal aorta, which is effectively rescued by low concentration of PI3K inhibitor, and by over-expression of dnPKA mRNA or vegf mRNA. Interestingly, mtmr8 expression is up-regulated when zebrafish embryos are treated with specific inhibitor of Hedgehog pathway that abolishes arterial marker expression. Conclusion: These data indicate that Mtmr8 is essential for vasculature development in zebrafish embryos, and may play a role in arterial specification through repressing PI3K activity. It is suggested that Mtmr8 should represent a novel element of the Hedgehog/PI3K/VEGF signaling cascade that controls arterial specification