橘园中重要天敌具瘤神蕊螨与其主要猎物的生态位

研究了柑橘园中具瘤神蕊螨(Agistemus exsertus)与其主要猎物柑橘皱叶刺瘿螨(Phyllocoptruta oleivora)、柑橘全爪螨(Panonychus citri)、柑橘粉虱(D ialeurodes citri)、黑刺粉虱(Aleurocanthus spiniferus)的生态位宽度、重叠和比例相似性。具瘤神蕊螨与其主要猎物相比,其时间和空间生态位宽度均最大,而其猎物中则以柑橘皱叶刺瘿螨的时间和空间生态位宽度最大,这表明具瘤神蕊螨和柑橘皱叶刺瘿螨的发生期较长,空间分布较广。具瘤神蕊螨与其猎物的生态位重叠在空间上与柑橘全爪螨的重叠值最大,在时间上与柑橘粉虱的重叠值最大。与其猎物相比,具瘤神蕊螨的时—空二维生态位宽度最大,在时空上占有明显的优势。     

神蕊螨属一新种述：（蜱螨亚纳：长须螨科）

本文记述神蕊螨属Ａｇｉｓｔｅｍｕｓ Ｓｕｍｍｅｒｓ一新种,黄山神蕊螨Ａｇｉｓｔｅｍｕｓ ｈｕａｎｇｓｈ－ａｎｅｎｓｉｓ ｓｐ．ｎｏｖ。     

中国神蕊螨属3新种1新记录（蜱螨亚纲：长须螨科）

描述了神螨属3新种,刺柏神蕊螨Agistemus juniperus sp.nov.青刚神蕊螨A.cy-cloblsnops sis sp.nov.黎川神蕊螨A.lichanen sis sp.nov.和中国1新记录种,泰国神蕊螨A.thaianus Eharaand Wongsiri,1984.     

神蕊螨属一新种记述(蜱螨亚纲:长须螨科)

本文记述神蕊螨属ＡｇｉｓｔｅｍｕｓＳｕｍｍｅｒｓ一新种,黄山神蕊螨Ａｇｉｓｔｅｍｕｓｈｕａｎｇｓｈａｎｅｎｓｉｓｓｐ．ｎｏｖ．。     

植物表面的毛对螨类的影响及其对害螨生防的启示

植物表面的毛可分为单细胞毛和多细胞毛(一般是腺毛)两大类。它们对植物上的螨类有直接或间接的影响。植物表面毛的作用可分为物理作用和化学作用:物理作用有影响活动、提供附着物(防止从叶面脱落)、提供隐蔽环境(防止捕食者捕食)、改善微环境(主要是维持叶面湿度)或捕捉并维持补充食物量(如花粉、菌类孢子)等形式;化学作用是毛本身所含的或受害螨为害后被诱导产生的化学物质对螨的生长发育和存活产生的影响,或作为有害螨存在的信号对捕食螨发挥作用。关于植物表面的毛对螨类的影响,国内研究得很少。国外的研究多数集中于各种植物上的毛对二斑叶螨Tetranychusurticae等害螨和智利小植绥螨Phytoseiuluspersimilis等捕食性螨的影响。植物表面的毛对螨类的影响很复杂。充分理解各种植物上的毛对螨类的影响可以获得关于害螨生物防治的重要启示。     

加州新小绥螨和巴氏新小绥螨对二斑叶螨的捕食能力比较

【目的】比较加州新小绥螨Neoseiulus californicus和巴氏新小绥螨Neoseiulus barkeri对二斑叶螨Tetranychus urticae的捕食能力,为果园二斑叶螨生物防治剂的选择提供依据。【方法】采用捕食功能反应的方法研究加州新小绥螨和巴氏新小绥螨雌成螨对二斑叶螨各螨态的捕食作用。【结果】加州新小绥螨和巴氏新小绥螨雌成螨对二斑叶螨各螨态的捕食功能反应均属于HollingⅡ型,对二斑叶螨各螨态的捕食能力均随着螨态的增大而降低,对卵的捕食能力最强,其次是幼螨、第一若螨、第二若螨、成螨。巴氏新小绥螨对二斑叶螨卵、幼螨的捕食能力强于加州新小绥螨,功能反应参数a/Th值分别高出55.2%和30.1%,而加州新小绥螨对二斑叶螨第一若螨、第二若螨的捕食能力强于巴氏新小绥螨,a/Th值分别高出67.5%和114.5%,两种捕食螨对二斑叶螨雌成螨的捕食能力相当,a/Th值均为4.5。加州新小绥螨和巴氏新小绥螨均对二斑叶螨的卵和幼螨表现出嗜食性,而对若螨和成螨没有嗜食性。两种捕食螨对二斑叶螨的捕食存在种内干扰,加州新小绥螨的干扰系数(0.328)大于巴氏新小绥螨(0.324)。【结论】在室内环境稳定的条件下,加州新小绥螨对二斑叶螨的捕食能力强于巴氏新小绥螨。     

黄瓜钝绥螨对茶黄螨雌成螨和腐食酪卵的功能反应

研究黄瓜钝绥螨Amblyseius cucumeris 对茶黄螨Polyphagotarsonemus latus (Banks)雌成螨和腐食酪螨Tyrophagus putrescentiae卵的功能反应。结果表明,黄瓜钝绥螨的第1若螨,第2若螨,雌成螨捕食茶黄螨雌成螨和腐食酪螨卵的功能反应均属于Holling II型,其中,雌成螨的捕食能力最强,对腐食酪螨卵和对茶黄螨雌成螨的攻击系数a大,处理时间th短,第2若螨也具有较强的捕食能力,对静态的腐食酪螨卵比对动态的茶黄螨捕食能力强,黄瓜钝绥螨对茶黄螨雌成螨具有很强的捕食能力。     

中国蜱螨学研究的回顾和展望

蝉螨亚纳（Acari）,包括蝉类（ticks）和螨类（mites）,是蛛形纲中最大的,也是生物多样性最为复杂的类群。地球上的各种生态环境,从陆地到海洋,从森林到土壤,从沙漠到河流,碑螨这一类微小的动物几乎无处不在。蝉螨种类极其繁多,估计种类数约100万种。蝉螨不但分布广泛,而且生活方式极为复杂。有些蝉螨寄生于人畜,吸食血液,是传播人畜疾病的重要媒介;也有的螨类取食植物,是农作物和林木的重要害螨;捕食性的螨类是害虫（螨）的天敌,是有利用价值的生物资源;自由生活的腐食性螨类对土壤有机物质的分解发挥着重要作用,在自然…     

两种植绥螨的同类相残和集团内捕食作用

巴氏新小绥螨(Neoseiulus barkeri)和黄瓜新小绥螨(N.cucumeris)是两种多食性植绥螨,主要捕食叶螨和蓟马等,目前在我国广泛应用于农业生物防治中.本文研究了这两种植绥螨种内的同类相残(cannibalism)和种间的集团内捕食作用(intraguild predation)以及相互之间的攻击强度,以明确两者之间的相互关系,为合理构建天敌组合及评估生物防治的作用提供依据.结果显示:两种植绥螨对同种或异种幼螨的捕食量最大,其次是若螨,而对卵的捕食量极低.两种植绥螨对异种幼螨或若螨的捕食量均极显著高于对同种幼螨或若螨的捕食量.可见,无其他猎物存在情况下,两种植绥螨同时发生时更倾向于发生种间的集团内捕食.而巴氏新小绥螨对异种幼螨或若螨的捕食量均高于黄瓜新小绥螨对异种幼螨或若螨的捕食量,并且巴氏新小绥螨和黄瓜新小绥螨相比,巴氏新小绥螨对异种幼螨的攻击性更强,因此当这两种植绥螨发生集团内捕食时,巴氏新小绥螨是潜在的集团内捕食者,而黄瓜新小绥螨是潜在的集团内猎物.     

丫蕊花属植物花粉和种子微形态特征比较及其分类学意义

采用光学显微镜和扫描电镜,对4种丫蕊花属植物(丫蕊花、小果丫蕊花、云南丫蕊花和高山丫蕊花)的种子微形态特征及表面纹饰等进行观察,并对除云南丫蕊花外的3种丫蕊花属植物花粉形态、大小、表面纹饰等微形态特征进行观察和比较分析,并讨论了花粉及种子微形态特征的进化生物学意义,为丫蕊花属植物物种间的分类学鉴定提供理论依据。结果表明:(1)丫蕊花属植物花粉形态多为长球形,少数为超长球形,赤道面观为椭圆形,极面观为圆形,花粉大小为(22~36.5)μm×(11.5~24)μm,花粉外壁纹饰为刺状颗粒。(2)丫蕊花的花粉较大,极轴明显长于其余种,小果丫蕊花极轴长度最小。(3)花粉外壁刺状颗粒纹饰在4种丫蕊花之间存在差异性特征。(4)丫蕊花属植物种子细梭形,两端具纤维状长尾,种皮表面纹饰为复网纹纹饰。(5)云南丫蕊花的种子最大,种脊显著;小果丫蕊花种子最小。(6)组成种子表面网纹纹饰的网脊、网壁及网眼的表面特征等在各物种间存在一定差异。     

嗜硫色谱分离纯化碱性脂肪酶及其氨基酸序列测定

扩展青霉(Penicillium expansum)FS1884所产生的碱性脂肪酶经硫酸铵沉淀、Sephacryl S-200柱层析后,再经嗜硫色谱(Thiophilic Chromatography)柱层析,被纯化了173．8倍,最终比活为5694．9U／mg。纯化后的脂肪酶达到了SDS-PAGE电泳纯、PAGE电泳纯以及毛细管液相色谱(Capillary Liquid Chromatography)纯。该脂肪酶N-端氨基酸序列测定的结果是：A T A D A A A F P D L H R A A K L S S A,与来自青霉属其它真菌脂肪酶一级结构作了比较。     

Characterization of a novel acidic protein of 38 kDa, A0, in yeast ribosomes which immunologically cross-reacts with the 13 kDa acidic ribosomal proteins, A1/A2

A new ribosomal protein of 38 kDa, named A0, was detected in yeast ribosomes on immunoblotting. The antibody used here was that against A1/A2, 13 kDa acidic ribosomal proteins which cross-reacted with A0. Although A0 and A1/A2 share common antigenic determinants, they differ in the following biochemical properties. While A1/A2 could be extracted from ribosomes with ethanol and ammonium sulfate, A0 could not. A0 gave two protein spots in a less acidic region than for A1/A2 on two-dimensional gel electrophoresis. The heterogeneity observed for A0 was ascribable to phosphorylation because one spot disappeared after treatment of the ribosomes with phosphatase. The syntheses of A0 and A1/A2 are directed by different mRNA species, as judged with a cell-free translation system, ruling out the possibility that A0 is a precursor of A1/A2. Although a mammalian ribosomal protein equivalent to A0 has been shown to be associated with 13 kDa acidic proteins in the cytoplasm, essentially no A0 was detected on immunoblotting in the yeast cytosol, while a small but detectable amount of A1/A2 was present. The possibility that A0 is a eukaryotic equivalent of L10 of Escherichia coli is discussed.     

Molecular analysis of HLA-A2.4 functional variant KLO: close structural and evolutionary relatedness to the HLA-A2.2 subtype

The structure of an HLA-A2.4 functional variant (A2.4c) expressed on donor KLO has been examined by comparative peptide mapping with other HLA-A2 antigens of known structure and radiochemical sequencing. All the peptide differences between A2.4c and A2.1 could be accounted for by five amino acid changes at positions 9, 43, 66, 95, and 156. The nature of residues 9, 43, and 95 in A2.4c was determined by sequencing to be identical to those in A2.2Y. The nature of residue 156 in A2.4c was also assigned as identical to that in A2.2Y on the basis of the identity of the corresponding peptide in its chromatographic comparison with A2.2Y. Position 66 was unique to A2.4c. It was determined to be an Asn residue instead of the Lys present in all other HLA-A2 antigens of known structure. This was the only detected amino acid difference between A2.4c and A2.2Y. The results indicate that, from a structural point of view, A2.4c is most closely related to the A2.2 subtype antigens and not to other A2.4 antigens. The data are compatible with the assumption that A2.4c was derived from A2.2Y by a single point mutation event.     

Immunochemical relatedness between secretory phospholipase A2 and intracellular phospholipase A2

The immunochemical relationship between rat pancreatic phospholipase A2 and rat splenic phospholipase A2 was examined with the use of anti-rat pancreatic phospholipase A2 antibody as a probe. The immunoelectrophoretic patterns showed that the antibody cross-reacted with the splenic enzyme. The immuno-crossreactivity was also shown by counter immunoelectrophoresis. The splenic phospholipase A2, whether it was purified from the cytosolic fraction or the microsomal fraction, formed an immunoprecipitin band with the anti-pancreatic phospholipase A2 antibody. The antibody was shown to inhibit the activity of the pancreatic phospholipase A2 as well as that of the splenic phospholipase A2.     

Occurrence of indole alkaloids among secondary metabolites of soil Aspergillus

The occurrence of indole alkaloids among secondary fungal metabolites was studied in species of the genus Aspergillus, isolated from soils that were sampled in various regions of Russia (a total of 102 isolates of the species A. niger, A. phoenicis, A. fumigatus, A. flavus, A. versicolor, A. ustus, A. clavatus, and A. ochraceus). Clavine alkaloids were represented by fumigaclavine, which was formed by A. fumigatus. alpha-Cyclopiazonic acid was formed by isolates of A. fumigatus, A. flavus, A. versicolor, A. phoenicis, and A. clavatus. The occurrence of indole-containing diketopiperazine alkaloids was documented for isolates of A. flavus, A. fumigatus, A. clavatus, and A. ochraceus. No indole-containing metabolites were found among the metabolites of A. ustus or A. niger.     

A quantitative method to evaluate neutralizer toxicity against Acanthamoeba castellanii.

A standard methodology for quantitatively evaluating neutralizer toxicity against Acanthamoeba castellanii does not exist. The objective of this study was to provide a quantitative method for evaluating neutralizer toxicity against A. castellanii. Two methods were evaluated. A quantitative microtiter method for enumerating A. castellanii was evaluated by a 50% lethal dose endpoint method. The microtiter method was compared with the hemacytometer count method. A method for determining the toxicity of neutralizers for antimicrobial agents to A. castellanii was also evaluated. The toxicity to A. castellanii of Dey-Engley neutralizing broth was compared with Page's saline. The microtiter viable cell counts were lower than predicted by the hemacytometer counts. However, the microtiter method gives more reliable counts of viable cells. Dey-Engley neutralizing medium was not toxic to A. castellanii. The method presented gives consistent, reliable results and is simple compared with previous methods.     

HCV NS5A基因表达及其在血清学检测中的应用评估

人丙型肝炎病毒 (ＨＣＶ)感染可引起丙型肝炎、肝硬化和肝细胞癌[1] 。丙型肝炎病毒是单股正链ＲＮＡ病毒 ,基因组约长 9.5ｋｂ ,仅有一个开放阅读框 ,编码一个大的聚蛋白前体 ,由宿主蛋白酶和病毒编码的蛋白酶加工成多个成熟蛋白。非结构蛋白ＮＳ5Ａ分子量为 56ｋＤ/ 58ｋＤ。目前对ＮＳ5Ａ蛋白的功能尚不清楚 ,ＮＳ5Ａ蛋白可降低干扰素治疗效果[2 ] ;ＮＳ5Ａ蛋白含核定位序列 ,因此人们推测它在ＨＣＶＲＮＡ复制过程中可能起一定的作用[3～ 4 ] 。本研究在大肠杆菌中表达全长ＮＳ5Ａ蛋白 ,提纯后ＮＳ5Ａ蛋白能与大多数丙肝阳性血清起强烈…     

HCV NS5A基因表达及其在血清学检测中的应用评估

Full-length NS5A gene of the hepatitis C virus was amplified by PCR using plasmid pBAC25 containing HCV nonstructural gene as template. The amplified fragment (about 1.34 kb) was cloned into plasmid pQE32, and the recombinant plasmid pQENS5A was expressed in JM109 strain. The NS5A protein was purified by NiSO4 metal chelating resin, and characterized by Western-blot. Its antigenecity was determined by ELISA. The positive detection rate of anti-NS5A was 75% (69/92) in ninety-two clinic sera. The positive rate of anti-NS5A was 82.5% (33/40) in fourty positive standand sera, and the negative rate of anti-NS5A was 100% (40/40) in fourty negative standand sera. The results showed that the Full-length NS5A proteinn had the higher sensitivity and specificity in the detection of HCV antibody in sera, we suggested that NS5A protein was a useful antigen for blood screening.