鱼类洄游通道恢复——国外的经验及中国的对策

简要介绍了鱼类洄游和鱼类洄游通道恢复的概念及类型。从法律与政策、资金筹措、恢复方法、恢复效果监测评估、信息交流与公众参与等5个方面介绍了欧盟、美、日、澳大利亚等国在鱼类洄游通道恢复方面积累的先进经验和成功实践,并在此基础上提出了我国鱼类洄游通道恢复应采取的对策:开展鱼类洄游通道恢复的立法和政策制定工作,加强鱼类洄游通道恢复工作的法律保障力度;开展流域阻碍鱼类洄游的障碍物调查和影响评价,制定流域鱼类洄游通道恢复规划;探索建立和完善多元化投入机制;加强鱼类洄游通道恢复研究能力建设,建立科学的技术支撑体系;开展

Genomic sequence of mandarin fish rhabdovirus with an unusual small non-transcriptional ORF

The complete genome of mandarin fish Siniperca chuatsi rhabdovirus (SCRV) was cloned and sequenced. It comprises 11,545 nucleotides and contains five genes encoding the nucleoprotein N, the phosphoprotein P, the matrix protein M, the glycoprotein G, and the RNA-dependent RNA polymerase protein L. At the 3' and 5' termini of SCRV genome, leader and trailer sequences show inverse complementarity. The N, P, M and G proteins share the highest sequence identities (ranging from 14.8 to 41.5%) with the respective proteins of rhabdovirus 903/87, the L protein has the highest identity with those of vesiculoviruses, especially with Chandipura virus (44.7%). Phylogenetic analysis of L proteins showed that SCRV clustered with spring vireamia of carp virus (SVCV) and was most closely related to viruses in the genus Vesiculovirus. In addition, an overlapping open reading frame (ORF) predicted to encode a protein similar to vesicular stomatitis virus C protein is present within the P gene of SCRV. Furthermore, an unoverlapping small ORF downstream of M ORF within M gene is predicted (tentatively called orf4). Therefore, the genomic organization of SCRV can be proposed as 3' leader-N-P/C-M-(orf4)-G-L-trailer 5'. Orf4 transcription or translation products could not be detected by northern or Western blot, respectively, though one similar mRNA band to M mRNA was found. This is the first report on one small unoverlapping ORF in M gene of a fish rhabdovirus. (c) 2007 Elsevier B.V. All rights reserved.

Gene structure and transcription of IRF-1 and IRF-7 in the mandarin fish Siniperca chuatsi

The genes of IRF-1 and IRF-7 have been cloned from the mandarin fish (Siniperca chuatsi). The IRF-1 gene has 4919 nucleotides (nt) and contains 10exons and 9introns, with an open reading frame (ORF) of 903 ntencoding301 aa. The IRF-7 gene has 6057 nt and also contains 10exons and 9introns, with an ORF of 1308 nt encoding 436 aa. The IRF-1 and IRF-7 genes have only one copy each in the genome. The transcription of IRF-1 and IRF-7 in different organs was analyzed by real-time PCR, and both molecules were constitutively expressed. The IRF-I and IRF-7 mRNAs were abundant in gill, spleen, kidney and pronephros. The temporal transcriptional changes for IRF-1, IRF-7 and Mx were investigated within 48 h after poly I: C stimulation in liver, gill, spleen and pronephros. An increased transcription was detected for IRF-1 and IRF-7 12 h post-stimulation, being earlier than the transcription of Mx protein; however, IRF-1 and IRF-7 transcription decreased while the Mx protein was stable at 48 h post-stimulation. (c) 2007 Published by Elsevier B.V.

Isolation and characterization of a rhabdovirus from co-infection of two viruses in mandarin fish

Co-infection of two viruses has been observed in mandarin fish (Siniperca chuatsi), but the two viruses have not been characterized. In this study, a rhabdovirus has been isolated from the co-infected two viruses extracted from the diseased mandarin fish, and its morphological structure and partial biochemical and biophysical characteristics have been observed and analyzed. The isolated rhabdovirus has a typical bullet shape, and is therefore called S. chttatsi rhabdovirus (SCRV). And, the isolated rhabdovirus produced a higher titer (10(8.5) TCID50 ml(-1)) than did the co-infecting viruses (10(6.5) TCID50 ml(-1)). Subsequently, the viral genome RNA was extracted, and used as template to clone the complete nucleoprotein (N) gene by RT-PCR amplification. Cloning and sequencing of the SCRV N protein revealed 42%-31% amino acid identities to that of trout rhabdovirus 903/87 and the rhabdoviruses in genus Vesiculovirus. SDS-PAGE separation of the isolated SCRV and other two rhabdoviruses also revealed obvious polypeptide profile difference. Moreover, the anti-SCRV N protein antibody was prepared, and the anti-SCRV N protein antibody only could recognize the SCRV N protein, whereas no antigenicity was detected in other two rhabdoviruses. The data suggested that the SCRV should be a rhabdovirus member related to the genus Vesiculovirus in the Rhabdoviridae. (c) 2006 Elsevier B.V. All rights reserved.

Frequency bandwidth estimation of TO packaging techniques for laser modules

Two simple methods for estimating the potential modulation bandwidth of TO packaging technique are presented. The first method is based upon the comparison of the measured frequency responses of the laser diodes and the TO laser modules, and the second is from the equivalent circuit for the test fixture, the TO header, the submount and the bonding wire. It is shown that the TO packaging techniques used in the experiments can potentially achieve a frequency bandwidth of over 10.5 GHz, and the two proposed methods give similar results.

Keyword spotting system based on biomimetic pattern recognition

The mandarin keyword spotting system was investigated, and a new approach was proposed based on the principle of homology continuity and point location analysis in high-dimensional space geometry theory which are both parts of biomimetic pattern recognition theory. This approach constructed a hyper-polyhedron with sample points in the training set and calculated the distance between each test point and the hyper-polyhedron. The classification resulted from the value of those distances. The approach was tested by a speech database which was created by ourselves. The performance was compared with the classic HMM approach and the results show that the new approach is much better than HMM approach when the training data is not sufficient.

漫反射农膜覆盖栽培效应

具有漫反射特性的塑料农膜(简称漫反射农膜)，是由性状特殊的结晶材料和常规成膜聚合物共混挤出成型而成的，是一种具有光转换效应、对可见光增透、红外光谱透过率比较

Wavelength Tuning in Two-Section Distributed Bragg Reflector Laser by Selective Intermixing of InGaAp-InGaAsP Quantum Well Structure

The two-section tunable ridge waveguide distributed Bragg reflector (DBR) laser fabricated by the selective intermixing of an InGaAsP-InGaAsP quantum well structure is presented. The threshold current of the laser is 51mA. The tunable range of the laser is 4.6nm, and the side mode suppression ratio (SMSR) is 40dB.

科尔沁沙地樟子松人工林土壤呼吸对水分变化的响应

土壤是陆地生态系统最大的碳库，其碳储量是大气碳储量的两倍。土壤呼吸是土壤碳库的最大输出途径。在干旱半干旱区降雨格局以及土壤水分条件的变化对土壤呼吸的影响具有重要意义。本研究以半干旱区科尔沁沙地东部樟子松人工林为研究对象，通过室内培养模拟研究、野外降雨量控制研究和降雨频率模拟及干湿交替模拟试验，研究了科尔沁沙地半干旱人工林生态系统土壤呼吸对水分变化的响应趋势，探讨了降雨格局变化对土壤呼吸的影响，结果表明： （1）土壤呼吸速率随温度和土壤含水量的升高分别呈指数和线性增长；温度和土壤含水量分别影响着土壤呼吸对土壤水分和温度的敏感性； （2）降雨量变化影响土壤呼吸日动态变化，降水量增加30%，土壤24h释放CO2量升高了35.9%，当降水量减少30%时，土壤24h释放的CO2量降低了59.6%，而且干旱降低了土壤呼吸日动态变化的幅度； （3）降雨量变化对土壤呼吸月季动态具有一定影响。降雨量增加30%，8~10月土壤总呼吸CO2释放速率升高40.7%~166.4%，土壤异养呼吸CO2释放速率升高40.5%~194.3%；降雨量降低30%使降雨较频繁的8月份土壤总呼吸CO2释放速率降低34.0%~70.0%，土壤异养呼吸CO2释放速率下降20.9%~ 64.0%，而在降雨较少的9~10月份降雨量的减少对土壤呼吸则没有显著影响； （4）降雨量的变化对土壤总呼吸和异养呼吸温度敏感性有一定影响。当降雨量减少30%时，土壤总呼吸的Q10值由5.4下降到2.22，土壤异养呼吸的Q10值由4.84下降到1.81； （5）用温湿度耦合作用经验模型Rt = 0.307e0.0064（W·T）来描述三个降雨处理样地土壤呼吸速率与土壤温度及土壤含水量的关系，可以解释土壤呼吸速率变异的80.2%； （6）在较高的温度条件下，降雨频率增加一倍时，土壤呼吸速率将升高约24%；当温度较低时，降雨频率对土壤呼吸速率的影响不显著； （7）土壤呼吸随着干旱程度的增加而逐渐下降，但当进行降水模拟后，土壤呼吸值迅速升高，可升高降水前的41.0% ~ 128%，而后又迅速下降，呈现明显的脉动（pulse）效应。