蚂蚁(膜翅目 :蚁科)的同巢识别与亲缘识别行为及机理概述(英文)

蚂蚁属真社会性昆虫。真社会性最主要的特性是在一个社会集团内个体间有生殖上的分工。即多数个体 (如工蚁 ,兵蚁等 )自身不行生殖 ,而一生“竭力”“帮助”少数个体 (如蚁后和雄蚁 )繁殖后代。蚂蚁生活的基本单位是社群 (colony)。一个单独的个体 (除创建蚁后 )是没有意义的。“典型”的社群由一个创建蚁后和其后代组成 (即单母 :monogyny)。单母社群内个体间亲缘关系密切。在自然界 ,多母社群 (polygyny)亦普遍存在。在多母社群里 ,如蚁后间亲缘关系密切 (如姐妹 ) ,社群内遗传关系同质性亦较高 ,个体间的平均遗传相关也密切。但如蚁后间亲缘关系疏远或无亲缘关系 ,那么社群内遗传异质性很高 ,个体间平均遗传相关也随之降低。和其它复杂的社会群体一样 ,蚂蚁社会拥有高度发达的通讯系统。社群不仅需要在内部个体间相互沟通以确保社群的平衡和协调性 ,而且必需和社群外各种息息相关的有机体间交流信息 ,以便有效利用有用的资源并避开各种危险。如果说信息素是蚂蚁通讯最重要的物质基础 ,那么对周围各类生物的识别便是蚂蚁通讯最为基本的环节。蚂蚁的识别行为及其机理是多样的 ,其生物学功能亦随被识别的对象不同而异。如 :为了确保社会群体的安全 ,蚂蚁必须准确识别“敌”、“我”和“朋友”。为了使得     

侧沟茧蜂属二新种记述(膜翅目:茧蜂科)(英文)

本文记述了采自甘肃、陕西杨凌、浙江松阳和福建福州等地的侧沟茧蜂属MicroplitisFoerster 186 2二新种 :赵氏侧沟茧蜂Microplitiszhaoi,sp .nov .,该新种与分布于古北区的MicroplitismalimbaPapp相似 ,但以下特征与之区别 :①前翅 1 R1脉短于翅痣长 ;②腹部第 1— 3腹片黄白色 ;③后肘室长为基宽的 2倍 ;④前翅r脉与 2 SR脉等长。其学名以我国著名寄生蜂分类学家赵修复教授姓氏命名。周氏侧沟茧蜂Microplitischoui ,sp .nov .,该新种与分布于东洋区的Microplitiszhaoi,sp .nov .相似但以下特征与之区别 ;①触角短于体长 ;②腹部第 1— 3腹片黑褐色 ;③腹部背板黑色 ;④前翅r脉短于 2 SR脉 ;⑤后翅cu a脉下端明显弯向翅基。其学名以我国著名昆虫分类学家周尧教授姓氏命名。模式标本保存在浙江大学植保系昆虫标本室。     

一种测定植物挥发物对棉铃虫引诱作用的无选择性风洞嗅觉仪(英文)

发展了一套测定棉铃虫Helicoverpaarmigera (H櫣ｂｎｅｒ)对植物挥发物的行为反应的生测系统。这套系统由嗅觉仪、风洞和风洞室组成。用这套系统测定了棉铃虫对萎蔫后的枫杨Pterocaryastenoptera叶、加拿大杨Populuscanadensis叶、香椿Toonasisnensis叶、新鲜的芹菜与胡萝卜花挥发物以及苯乙醛的行为反应。结果显示 ,萎蔫的枫杨叶、加拿大杨叶、香椿叶的挥发物均对棉铃虫处女雌蛾表现出显著的引诱作用 ,而对已交配过的雌蛾和雄蛾无明显的引诱作用 ;新鲜的芹菜与胡萝卜花挥发物对棉铃虫两性性成虫均不表现出显著的引诱作用 ;苯乙醛对棉铃虫处女雌、雄蛾有较强的引诱作用。讨论了杨树枝把引诱棉铃虫的原因。     

棉蚜DNA多态性RAPD PCR分析(英文)

应用RAPD PCR技术研究了不同寄主和不同季节棉蚜的DNA多态性。从 2 0种随机引物中筛选出 3种引物 ,用它们的扩增结果进行Nei的遗传距离计算 ,并根据遗传距离对所研究的棉蚜种群做聚类分析。结果表明南京地区花椒上的棉蚜与其它 4种寄主上的棉蚜在DNA水平有明显的分化。聚类分析表明 ,棉蚜季节性种群可分为 3大类群 ,即春、秋季黄色型 ,春、秋季绿色型和黄色小型蚜 (伏蚜 )。而小型蚜的遗传关系与春、秋季绿色型最为接近。     

昆虫病原斯氏和异小杆线虫对各种非共生微生物的信息反应(英文)

非线虫共生细菌 (Bacillussubtilis ,B .thuringiensis,Pseudomonasfluorescens ,Micromonosporapur purea,Rhizopusdelemar ,Pseudomonasaeruginosa ,Streptomycesvenezuelae ,Streptomycesantibioticus ,Penicilliumcitrnum ,Ganodermalucidum ,Agaricusbisporus,Pleurotusostreatus,Rhizobiumlegumi unosarum和Photobacteriumphosphoreum)的培养液以及其上清液、斜纹夜蛾 (Spodopteralitura)昆虫细胞系用于引诱无菌SteinernemacarpocapsaeA2 4和HeterorhabditisbacteriophoraH0 6发育。上述培养物均未能诱导H .bacteriophoraH0 6发育。虽然P .phosphoreum菌液可致死A2 4线虫 ,但是其上清液可诱导线虫发育。无菌S .carpocapsaeA2 4线虫可利用斜纹夜蛾昆虫细胞繁殖 ,产生下一代感染期线虫。结果进一步说明 ,引诱H .bacteriophoraH0 6发育的化学信息物质比S .carpocapsaeA2 4的专一。     

人血管生成素-PE40融合蛋白基因的构建、表达及活性研究

利用 PCR扩增出人血管生成素 (h ANG)成熟肽的基因片段 .与绿脓杆菌外毒素缺失突变体PE40的基因连接后 ,克隆入 p UC1 9载体中 .测序后克隆入表达载体 p RSETB,构建成 h ANG-PE40融合基因的表达载体 .IPTG诱导 ,表达出分子量约为 58k D的 His6- ANG- PE40融合蛋白 ,占菌体总蛋白的 8% .Ni2 +- NTA树脂纯化表达蛋白 ,SDS- PAGE结果显示纯化重组蛋白为单一条带 .鸡胚绒毛尿囊膜鉴定表明重组蛋白体外能够有效地抑制血管的形成 .     

肌醇磷脂激酶(PI4-K)单克隆抗体的制备及其对细胞生长的抑制

制备了抗肌醇磷脂激酶 ( PI4- K)单克隆抗体 ( A6D)并测定了抗原 -抗体反应基本特性及功能 .结果表明 ,单克隆抗体与固相及溶液中肌醇磷脂激酶的亲和常数分别为 7.5× 1 0 6和 6× 1 0 8( mol/L) -1.单抗 1 .9× 1 0 -7mol/L可以抑制从细胞提取液的 PI4- K酶活力 50 % .用 FITC标记单抗在蛋白微球引导下进入细胞内 ,主要富集在细胞质膜区 ,并对 He La细胞和小鼠小脑细胞生长有明显抑制作用 .     

普遍野生稻和亚洲栽培稻遗传多样性的研究

用 ４４个 ＲＦＬＰ标记对来自中国、印度、泰国等亚洲 １０个国家的普通野生稻（简称普野,下同）和来自多个国家的７５个栽培稻品种,从多态位点的比率、等位基因数、基因型数、平均杂合度及平均基因多样性等多个方面,比较了不同国家和不同地区的普通野生稻、栽培稻籼粳亚种及栽培稻与普野之间遗传多样性的差异。结果表明：中国普野的遗传多样性最大;其次是印度普野;南亚普野的平均基因多样性大于东南亚普野,而多态位点的比率、等位基因数及基因型数等却低于东南亚普野;栽培稻的遗传多样性明显小于普通野生稻。在所检测的４４个位点中,栽培稻的多态位点数仅为野生稻的３／４,等位基因数约为野生稻的６０％,基因型种类约为野生稻的１／２。栽培稻中籼稻的遗传多样性高于粳稻。在平均每个位点的实际杂合度上,以中国普野杂合度最高,普通野生稻是栽培稻的２倍。说明从野生稻演化成栽培稻的过程中,经过自然选择和人工选择,杂合度降低,等位基因减少,基因多样性下降。     

Effect of Different Levels of Pressure Relieving Air-Mattress Firmness on Cough Strength

Cough is an important host-defense mechanism. The elderly and patients who are severely ill cannot cough effectively when lying in the supine position. Furthermore, pressure relieving air-mattresses are recommended for preventing the development of pressure ulcers. In this study, we clarified whether or not the cough peak flow (CPF), an index of cough strength, is affected by different firmness levels of a pressure relieving air-mattress in healthy volunteers in the supine position. Fifty-two healthy young men participated. All the measurements were carried out on each participant in the supine position on a pressure relieving air-mattress. The participants were assessed at two firmness levels, a “hard” and “soft” mode. The CPF, forced vital capacity (FVC), maximal expiratory pressure (PEmax), and maximal inspiratory pressure (PImax) were determined for each mode. The sinking distance of the body into the mattress was measured without any activity and the difference between the sinking distances of the two firmness levels was determined. The CPF, FVC, PEmax, and PImax were determined for each mode. The sinking distance of the body into the mattress was measured and the difference between the sinking distances of the two firmness levels was determined. The CPF, FVC, PEmax and PImax values of the participants coughing on the mattress were significantly lower when the mattress was in “soft” than in “hard” mode. The differences between the sinking distances of the mattress in “soft” and “hard” modes were larger for the anterior superior iliac spine. A harder mattress may lead to increased CPF in healthy young men lying in the supine position, and increased CPF may be important for host defense.     

Topological Localization of Monomeric C-reactive Protein Determines Proinflammatory Endothelial Cell Responses

The activation of endothelial cells (ECs) by monomeric C-reactive protein (mCRP) has been implicated in contributing to atherogenesis. However, the potent proinflammatory actions of mCRP on ECs in vitro appear to be incompatible with the atheroprotective effects of mCRP in a mouse model. Because mCRP is primarily generated within inflamed tissues and is rapidly cleared from the circulation, we tested whether these discrepancies can be explained by topological differences in response to mCRP within blood vessels. In a Transwell culture model, the addition of mCRP to apical (luminal), but not basolateral (abluminal), surfaces of intact human coronary artery EC monolayers evoked a significant up-regulation of MCP-1, IL-8, and IL-6. Such polarized stimulation of mCRP was observed consistently regardless of EC type or experimental conditions (e.g. culture of ECs on filters or extracellular matrix-coated surfaces). Accordingly, we detected enriched lipid raft microdomains, the major surface sensors for mCRP on ECs, in apical membranes, leading to the preferential apical binding of mCRP and activation of ECs through the polarized induction of the phospholipase C, p38 MAPK, and NF-κB signaling pathways. Furthermore, LPS and IL-1β induction of EC activation also exhibited topological dependence, whereas TNF-α did not. Together, these results indicate that tissue-associated mCRP likely contributes little to EC activation. Hence, topological localization is an important, but often overlooked, factor that determines the contribution of mCRP and other proinflammatory mediators to chronic vascular inflammation.