高压扭转铜试样的微观组织与压缩性能

通过高压扭转对铜试样施加不同程度的变形，研究了样品扭转面（ND面）和纵截面（TD面）上微观组织特征．对ND面，在较小的剪应变下，原始晶粒形貌模糊，晶粒内部形成等轴状的位错胞及亚晶结构；随变形量的增大，亚晶间取向差及亚晶内部的位错密度增大，最后形成亚微米尺度的等轴晶粒．对TD面，变形初期原始晶粒被拉长，晶粒内部为位错墙分割成的层状结构，层内为拉长的位错胞；随变形程度的增大，拉长晶粒的宽度减小，与剪切方向的夹角减小，晶内层状组织间距减小，并逐渐演化成拉长的亚晶组织；进一步增大变形，晶粒拉长痕迹消失，变形组织与ND面相似，为等轴状亚微米晶粒．压缩实验表明，经16圈扭转后，整个试样上的压缩性能基本均匀，σ0．2达到385MPa，应变率敏感性指数增大至0．021．

Influence of LiB3O5 structure on microstructure and optical properties of ZrO2, thin films prepared by electron beam evaporation

ZrO2 thin films were deposited bill using an electron beam evaporation technique on three kinds of lithium triborate (LiB3O5 or LBO) substrates with the surfaces at specified crystalline orientations. The influences of the LBO structure on the structural and optical properties of ZrO2 thin films are studied by spectrophotometer and x-ray diffraction. The results indicate that the substrate structure has obvious effects on the structural end optical properties of the film: namely. the ZrO2 thin film deposited on the X-LBO, Y-LBO and Z-LBO orients to m(-212), m(021) and o(130) directions. It is also found that the ZrO2 thin film with m(021) has the highest refractive index and the least lattice misfit.

LBO晶体上ZrO2薄膜的显微结构和光学性质

用电子柬蒸发方法在三种不同取向的三硼酸锂（LiB3O3，简称LBO）晶体上沉积了ZrO2薄膜。采用分光光度计和X射线衍射技术对LBO晶体基底结构对薄膜光学性质和显微结构的影响进行了研究。实验结果表明：基底结构对薄膜的显微结构和光学性质具有明显影响，即X-LBO，Y-LBO和Z-LBO上沉积的ZrO3薄膜分别沿m（-212），m（021）和o（130）择优生长，且m（021）择优取向的ZrO3薄膜具有最高的折射率和最小的晶格不匹配。

青蒿素含量影响因子分析及青蒿生殖结构的研究

由于青蒿中青蒿素含量很低，造成生产上成本过高，限制了青蒿素的应用。因此找到青蒿素含量的影响因子，并利用这些因子提高青蒿素含量是十分必要的。 研究青蒿有性生殖过程和生殖结构能够为青蒿遗传育种方面的研究提供理论依据。 利用青蒿高产株系001的茎段作为外植体，通过诱导丛生芽的方法得到无性克隆系s．，利用s．进行了青蒿素含量影响因子的研究。发现在Hoagland培养液中添加0. 44mg/L浓度的ZriS04.7H20,5.72 mg/L的HB03,0.32 mg/L的CuS04.5H20或者5uLmol／L的茉莉酸甲酯时能够明显提高青蒿素含量。 一些试验结果表明青蒿素含量不但受到培养条件的影响，而且和青蒿自身的生长发育有很大的关系。青蒿素含量在营养生长阶段随着青蒿的生长而逐步提高，当每天日照长度短于临界日长一16.5小时，青蒿进入生殖生长阶段，青蒿素含量短日照处理的第9-18天最高，而这一阶段也恰好是青蒿花蕾出现和发育的时期，此后青蒿素含量持续变低。青蒿素在青蒿植株不同器官中含量不同，其中叶片青蒿素含量最高，花蕾中也较高，但茎中含量极低。在不同部位的叶片中含量由高到低的顺序为中部叶片》下部叶片》上部叶片。青蒿植株不同部位器官中青蒿素含量的差异可能和这些部位腺毛数量的差异有关。 遗传差异是导致青蒿各个植株间青蒿素含量差异的主要原因。对青蒿素低产（02卜1，021-5）高产02卜18, 02卜19, 021-20）的五个青蒿株系进行了RAPD研究，以中间型产量02卜g和02卜d两个株系作对照。用OPRON公司的A，B，c，D，K五组100条随机引物进行PCR扩增。发现OPA15 (5' TTCCGAACCC 3')能在所有高产株系中扩增到一条lOOObp的条带，而在低产株系中则扩增不到这条带。这个条带很可能是高产青蒿株系特有的条带( OPA151000)，并有可能作为高产株系的分子标记。 利用整体透明和石蜡切片技术对青蒿的生殖结构进行了研究，研究表明青蒿的头状花序球形，直径大约2—3mm。两性花10-30朵，单层花冠合生，开放时顶端5裂，内有5枚聚合雄蕊。一枚雌蕊，柱头两裂。单性雌花10-18朵，花冠舌状，雄蕊退化。两种花都是子房下位，单室倒生型胚珠。 雌配子体的的发育过程，大孢子母细胞经过减数分裂形成二分体和四分体，四分体中合点端的一个发育成具功能的大孢子，其它三个分解掉，胚囊发育成单核胚囊。然后通过三次有丝分裂经过二核胚囊、四核胚囊阶段发育到八核胚囊，最后形成七细胞、八核胚囊。卵细胞和两个助细胞组成卵器分布在珠孔端，而三个反足细胞分布在合点端。 小孢子母细胞经过两次减数分裂形成二分体和四分体，四分体中的小孢子释放出来后发育成单核花粉，单核花粉经过有丝分裂发育成二核花粉和三核花粉。

紫茎泽兰种子库及幼苗动态特征

紫茎泽兰（Eupatorium adenophorum）是臭名昭著的世界性恶草之一，目前已对全世界30多个国家和地区造成入侵危害，大约在20世纪30年代入侵我国，在我国西南地区造成了严重的危害。本文以四川省攀枝花市遭受紫茎泽兰入侵危害严重的生态系统为研究对象，分别对不同生境下的紫茎泽兰土壤种子库进行调查，以探究紫茎泽兰土壤种子库的结构，并分析人类干扰对土壤种子库结构的影响。并在种子库调查的基础上设计了两项盆栽实验，研究紫茎泽兰土壤种子库的结构的改变导致的紫茎泽兰种子环境因子的改变，从而影响紫茎泽兰种子的萌发、幼苗的命运，以期阐明人类干扰对紫茎泽兰入侵的影响。另外连续测定紫茎泽兰早期生长的生物量，研究紫茎泽兰生物量增长、分配规律，并与其它几种本地种相比较，说明紫茎泽兰能够入侵成功的原因。 在攀枝花紫茎泽兰入侵严重的地区，通过取样研究果园、放牧灌丛以及禁牧灌丛3种不同生境紫茎泽兰土壤种子库特征，发现这3种生境的土壤种子库大小分别为10422粒m-2，3522粒m-2和2889粒m-2 。果园、放牧灌丛和禁牧灌丛等3种干扰程度不同生境的深层种子量占总种子量的比例分别为56.44%，46.96%，24.86%（p=0.006）。从干扰程度上来说，由于果园>放牧灌丛>禁牧灌丛，这一结果表明土壤深层种子量大小与干扰成正比，干扰越大，深层次紫茎泽兰种子量占总种子量的比重越大。由此可以推测，人类的干扰使得紫茎泽兰土壤种子库结构发生了改变，一方面人类干扰导致生境植被覆盖不同，干扰越大，植被覆盖度越小，土壤种子库越大，另一方面人类活动对土壤的直接扰动，使土壤种子库结构发生变化，在放牧灌丛和果园2种生境中，由于人类活动的影响，促使了紫茎泽兰土壤种子库表层种子向下层转移，而且转移量与干扰程度成正相关。由于一定深度埋藏的紫茎泽兰种子萌发的幼苗具有较低的死亡率，进入土壤深层的紫茎泽兰种子越多，紫茎泽兰的长久性土壤种子库就越大，对紫茎泽兰幼苗的补充和定居越有利，入侵也就越难以治理。 初步研究了光照、水分和种子在土壤中的埋藏深度等对紫茎泽兰幼苗的影响，结果发现，1) 播种在0cm、2cm、5cm深度的种子萌发率分别为64.67%、22.67%、13.33%，即种子埋藏越深，萌发率越低，不同层次种子萌发率差异极显著(p=0.00)；幼苗死亡率分别为27.95%、0、0，表层种子萌发的幼苗有较高的死亡率，而由埋藏在深层种子萌发的幼苗没有死亡，土壤表层发芽的幼苗与不同埋藏深度种子萌发的幼苗之间死亡率差异极显著(p=0.00)；2) 在无遮蔽、半遮蔽、全遮蔽3种不同情况下，紫茎泽兰幼苗的死亡率分别为72.15%、30.38%、4.87%，定居率分别为6.66%、33.99%、46.67%，即遮蔽程度越高，死亡率越低，定居率越高，不同处理之间死亡率和定居率差异均极显著（p=0.00）；3) 在浇水、不浇水这2种水分条件下紫茎泽兰的萌发率分别为41.56%、32% (p=0.021)；死亡率分别为35.8%、35.23% (p=0.934)；定居率分别为29.11%、22.66% (p=0.083)，说明水分因子对萌发率的影响显著，对死亡率、定居率的影响不显著。上述结果表明，土壤埋藏深度、光照和水分都是影响紫茎泽兰幼苗萌发的重要因素：一定深度的土壤埋藏能够有效降低紫茎泽兰幼苗的死亡率；光照强度与紫茎泽兰幼苗死亡率成正相关；而水分对紫茎泽兰幼苗的存活影响不显著。 通过跟踪调查紫茎泽兰的早期生长的生物量，发现紫茎泽兰生物量和高度增加迅速,且生物量的增加主要来自地上部分量的增加，而本地灌木却生长缓慢。与本地种相比，紫茎泽兰的根冠比很小，在生殖分配上，紫茎泽兰与本地灌木相比又比较大。另一方面，在生长季到来的时候，紫茎泽兰能够迅速生长，并将大部分生物量分配到地上部分；而在旱季，当许多本地本植物由于枯死、休眠进入休眠状态时，紫茎泽兰却能继续生长，从而确保其在竞争中的空间优势。 综上所述，人类活动的干扰可能导致更多的紫茎泽兰种子进入土壤深层，从而改变了紫茎泽兰土壤种子库的结构；种子萌发后强光直射可能是导致紫茎泽兰幼苗死亡的重要原因；由于土壤深层种子比表层种子具有更强的抵抗强光照射等不良环境因子影响的能力，所萌发的幼苗成活率高，表明其具有更高的繁殖效率。因此可以说是人类活动的干扰不但加剧了紫茎泽兰的入侵，也使得紫茎泽兰入侵后难以根除。

蛙虹彩病毒cop基因的克隆表达及亚细胞定位

从蛙虹彩病毒(Rana gryliovirus,RGV)基因组中克隆了含凋亡相关结构域的新基因-cop(Caspaserecruit ment domain only protein,COP)基因的全部编码区,成功构建了重组表达载体,进行了原核表达,并在鲤鱼上皮瘤细胞(Epithelioma papulosumcyprini,EPC)中进行了亚细胞定位.序列分析表明,RGVcop基因全长288 bp,编码一个长为95 aa,分子量为10.4×103的推定蛋白.二级结构预测表明其含有5个α螺旋.同源性比对分

复合垂直流构建湿地中生物膜的空间分布、特性和降解性能

对复合垂直流构建湿地基质不同层次进行采样,测定了生物膜的空间分布、脱氢酶活性、呼吸强度、间隙水总有机碳、发育时间及五氯酚的去除率等指标.结果表明,基质生物膜发育良好,可挥发性固体均值达到0.021 8.从下行池整体看,生物膜生物量、呼吸强度、脱氢酶活性及有机污染物去除能力都较上行池高,下行池为污水中有机物的主要降解空间.不同层次生物膜的空间分布存在着差别,生物膜主要积累在0~10 cm表层,其脱氢酶活性、呼吸强度高于其他各层次,各指标在变化趋势上存在明显的一致性.生物膜的发育时间直接影响着其对有机碳的降解

长江中游草鱼天然种群的生化遗传结构及变异

采用淀粉或聚丙烯酰胺凝胶电泳方法分析了长江中游武汉江段草鱼天然种群(n=81)中10种同工酶约28个基因座位的遗传变异型。该种群的多态座位比例为16.7%,平均杂合度为0.0739。而Utter和Folmar(1978)曾报道美国的5个草鱼人工繁殖种群的多态座位比例及平均杂合度分别为6%和0.021。比较结果表明,近交很可能是导致草鱼人工繁殖种群中遗传变异性降低的主要原因。我们认为生产上采用数量大、来源广的亲鱼进行人工繁殖,并定期用天然种群更换或补充繁殖用亲鱼很可能是保持或增加鱼类人工繁殖种群遗传变异性的

鲢和鳙的氮平衡研究——Ⅰ.在高温季节(夏季)氮平衡几个参数的测定

高温季节,在静止吋(摄食状态)的氮代谢方程式鲢为Mg=0.054W~(0.884)(毫克-氮/小时);鳙为Mg=0.073 W~(0.782)(毫克-氮/小时);氮的运动代谢量随游泳速度(s)的增大呈指数增长。氮的收支公式鲢为0.44 C_N=0.181 W~(0.61)+24/0.75{0.054-0.021(1-e~(0.2168)}W~(0.884);鳙为0.57 C_N=1.98 W~(0.61)+24/0.75{0.075-0.033(1-e~(0.1798)}W~(0.782)。以鲢和鳙对微囊

Grass carp reovirus activates RNAi pathway in rare minnow, Gobiocypris rarus

Dicer catalyzes the initiation step of RNA interference (RNAi) which is known to play a significant role in innate immune response to viral infection in many organisms. To study the RNAi-related pathway after virus infection in fish, we identified a partial cDNA sequence of dicer from rare minnow, Gobiocypris rants. Real-time quantitative RT-PCR (qRT-PCR) demonstrated the Dicer transcript level was the highest at zygote stage, decreased at prim-5 stage, and was stable from the protruding mouth to adult stage. Regular RT-PCR analysis showed that the Dicer gene expressed widely in the tested tissues, including brain, gill, heart, intestine, kidney, liver, muscle, ovary, spleen and testis. The expression of Dicer mRNA was significantly increased in the early period of Grass carp reovirus (GCRV) infection, and declined from 24 It post-injection (h p.i.) (P<0.05). The mRNA expression returned to control levels at 48 h p.i. (P>0.05). Under transmission electron microscope, virions were difficulty to find out in 12 h p.i., and virus inclusion bodies and few scattered viral particles were easily visualized from 24 h p.i. to moribund. These results implied GCRV triggered the RNAi pathway in the early stages of infection and perhaps virus inclusion bodies suppressed the antiviral functions of RNAi mechanism. (C) 2009 Published by Elsevier B.V.

Zebrafish peptidoglycan recognition protein SC (zfPGRP-SC) mediates multiple intracellular signaling pathways

Insect PGRPs can function as bacterial recognition molecules triggering proteolytic and/or signal transduction pathways, with the resultant production of antimicrobial peptides. To explore if zebrafish peptidoglycan recognition protein SC (zfPGRP-SC) has such effects, RNA interference (siRNA) and high-density oligonucleotide microarray analysis were used to identify differentially expressed genes regulated by zfPGRP-SC. The mRNA levels for a set of genes involved in Toll-like receptor signaling pathway, such as TLRs, SARM, MyD88, TRAF6 and nuclear factor (NF)-kappa B2 (p100/p52), were examined by quantitative RT-PCR (QT-PCR). The results from the arrays and QT-PCR showed that the expression of 133 genes was involved in signal transduction pathways, which included Toll-like receptor signaling, Wnt signaling, BMP signaling, insulin receptor signaling, TGF-beta signaling, GPCR signaling, small GTPase signaling, second-messenger-mediated signaling, MAPK signaling, JAK/STAT signaling, apoptosis and anti-apoptosis signaling and other signaling cascades. These signaling pathways may connect with each other to form a complex network to regulate not just immune responses but also other processes such as development and apoptosis. When transiently over-expressed in HEK293T cells, zfPGRP-SC inhibited NF-kappa B activity with and without lipopolysacharide (LPS) stimulation. (C) 2008 Elsevier Ltd. All rights reserved.

Isolation and characterization of Argonaute 2: A key gene of the RNA interference pathway in the rare minnow, Gobiocypris rarus

Argonaute 2 gene plays a pivotal role in RNAi in many species. Herein is the first report of the cloning and characterization of Argonaute 2 gene in fish. The full-length cDNA of Gobiocypris rarus Argonaute 2 (GrAgo2) consisted of 3073 nucleotides encoding 869 amino acid residues with a calculated molecular weight of 98.499 kDa and an estimated isoelectric point of 9.18. Analysis of the deduced amino acid sequence showed the presence of two signature domains, PAZ and Piwi. RT-PCR analysis indicated that GrAgo2 mRNA expression could be detected in widespread tissues. After infection with grass carp reovirus, GrAgo2 expression was up-regulated from 12 h post-injection (p < 0.05) and returned to control levels at 48 h post-injection (p > 0.05). These data imply that GrAgo2 is involved in antiviral defense in rare minnow. (C) 2008 Published by Elsevier Ltd.

Characterization of C-C chemokine receptor subfamily in teleost fish

Chemokines and their receptors play important roles in nervous and immune systems. Little information, however, exists concerning this gene family in teleost fish. In the present Study, 17 C-C chemokine receptors genes were identified from Danio rerio, 9 from Gasterosteus aculeatus, 10 from Oryzius latipes, 8 from Takifugu rubripes and 5 from Tetraodon nigroviridis. Phylogenetic analysis showed that the orthologs to mammalian CCR6, 7, 8, 9 and CCRL1 receptors were evident in zebrafish, but the clear orthologs to mammalian CCR1, 2, 3, 4, 5 and 10 were not found in zebrafish. The gene structure of zebrafish CCR (zfCCR) was further analyzed. The open reading frame of zfCCR3-1, zfCCR3-3, zfCCR6-1, zfCCR6-2, zfCCR8-2 contain one exon, and two exons were identified for zfCCR2-1, zfCCR2-2, zfCCR4 and zfCCRLI-1, three exons for zfCCR3-2, zfCCR5 and zfCCR7, four exons for zfCCR8-1 and zfCCR9-1. The expression analyses showed that in zebrafish, most C-C chemokine receptor genes Were expressed in fertilized eggs and oocytes, and all the receptor genes were expressed in larval stages. The zfCCR2-2, zfCCR3-1, zfCCR4 and zfCCR6-2 genes were expressed in all normal organs examined, whereas not for zfCCR2-1, zfCCR3-3, zfCCR6-1, zfCCR8-1, zfCCR9-2 and zfCCRL1-2. The expression of zfCCR3-2, zfCCR5, zfCCR7, zfCCR9-1 and zfCCRLI-1 were detected in the majority organs. and zfCCR8-2 and zfCCR8-3 detected only in brain. The differential expression pattern of different paralogues in organs may indicate their difference in function, which requires further investigation. (C) 2008 Elsevier Ltd. All rights reserved.

Establishment of a Chinese sturgeon Acipenser sinensis tail-fin cell line and its susceptibility to frog iridovirus

Chinese sturgeon Acipenser sinensis, a cartilaginous ganoid, is a 'living fossil' on a deeply isolated evolutionary branch. A cell line was established from Chinese sturgeon tail-fin tissue (CSTF) . These epithelial CSTF cells grew well in Dulbecco's modified Eagle's medium at 25 degrees C. Karyotypic analysis revealed a normal diploid karyotype with 2n = 264 and large numbers of punctate chromosomes. A strain of frog iridoviruses [Rana grylio virus (RGV)] was used to test the susceptibility of this cell line to infection. Infection was confirmed by cytopathic effect, immunofluorescence and electron-microscope observations, which detected the viral antigens or particles in the cytoplasm of RGV-infected cells. Molecular analysis further suggested that c. 550 bp DNA fragment could be cloned from the RGV-infected CSTF cells' DNA with major capsid protein gene polymerase chain reaction primers. Furthermore, after transfection with pEGFP vector DNA, the CSTF cell line produced significant fluorescent signals indicating its utility in exogenous studies.

RNAi suppression of zebrafish peptidoglycan recognition protein 6 (zfPGRP6) mediated differentially expressed genes involved in Toll-like receptor signaling pathway and caused increased susceptibility to Flavobacterium columnare

In Drosophila, Toll signaling cascade, which resembles the mammalian Toll-like receptor (TLR)/IL-1R signaling pathways and regulates the expression of anti-microbial peptide genes, mainly relies on peptidoglycan recognition proteins (PGRPs) for the detection of bacterial pathogens. To explore the effect of zebrafish peptidoglycan recognition protein 6 (zfPGRP6) on Toll-like receptor signaling pathway, RNA interference (siRNA) and real time quantitative PCR (RQ-PCR) methods were used to identify differentially expressed genes regulated by zfPGRP6. The target genes included TLR2, TLR3, TLR5, TLR7, TLR8, IL1R, Sterile-alpha and Armadillo motif containing protein (SARM), myeloid differentiation factor 88 (MyD88) and nuclear factor (NF)-kappa B2 (p100/p52). The results of RQ-PCR showed that RNAi-mediated Suppression of zfPGRP6 significantly down-regulated the expression of TLR2, TLR5, IL1R, SARM, MyD88 and p100/p52. The expression of beta-defensin-1 was also down-regulated in those embryos silenced by zfPGRP6. In challenge experiments to determine the anti-bacterial response to Gram-negative bacteria, RNAi knock-down of zfPGRP6 markedly increased susceptibility to Flavobacterium columnare. (C) 2008 Elsevier B.V. All rights reserved.