番茄裂果机理及防治措施

从番茄裂果的遗传因素、生理特性、环境条件、栽培措施等方面分析了番茄裂果发生的原因,并提出了相应的防治措施.     

番茄红素研究概况

番茄红素是开链式的类胡萝卜素,具有清除活性氧自由基、促进细胞间隙连接通讯、防癌抗癌等多种生理功能。作为一种功能性天然色素,番茄红素被广泛地用于多种功能性食品。文章主要介绍了番茄红素的研究历史、理化性质及生理功能,对番茄红素的应用前景进行了展望。     

长期咸水灌溉对土壤酶活性及反应动力学的影响

为了探讨咸水灌溉导致土壤质量下降的原因,研究了5个含盐量水平(1.25(对照)、2.50、5.00、7.50d S·m~(-1)和10.00 d S·m~(-1))的咸水长期田间污染对0~20 cm和20~40 cm土壤水解酶活性及酶促反应动力学性质的影响。结果表明:咸水灌溉导致土壤脲酶、β-葡糖苷酶和碱性磷酸酶活性呈现不同程度的降低,与对照相比,10d S·m~(-1)咸水灌溉下0~20 cm土壤层三种酶活性分别下降45.5%、50.8%和24.9%,20~40 cm土壤层三种酶活性分别下降37.44%、32.1%和21.8%;咸水灌溉改变了土壤酶的催化动力学特性,与对照相比,10 d S·m~(-1)咸水灌溉下脲酶、β-葡糖苷酶和碱性磷酸酶的最大反应速度V_(max)分别下降47.77%、44.62%和15.01%,Km分别下降57.12%、保持不变和下降14.64%,β-葡糖苷酶V_(max)/K_m下降39.63%,脲酶和碱性磷酸酶的V_(max)/K_m没有显著变化。数据表明咸水灌溉对不同的酶抑制机制不尽相同。     

垂序商陆及胜红蓟提取物对降香黄檀炭疽病菌的抑菌机理研究

通过测定垂序商陆与胜红蓟乙酸乙酯提取物处理后的降香黄檀炭疽病菌内丙二醛含量、蛋白质含量以及4种酶活性,来初步判断垂序商陆与胜红蓟提取物对炭疽病菌的作用机理。结果表明:两种提取物都能在一定程度上破坏炭疽病病原菌膜系统,垂序商陆处理组丙二醛含量在56h后显著提高,胜红蓟处理组则缓慢增加,略高于对照组;垂序商陆处理组菌体内蛋白质含量先增加,32h后急剧降低,胜红蓟处理组蛋白质含量从初期开始就少于对照组;两种提取物都能影响菌体的保护性酶活性,两处理组SOD活力都呈现先增高后降低的趋势,CAT活力高于对照组。两组SDH、LDH活力都小于对照组,而垂序商陆处理组SDH、LDH活力小于胜红蓟处理组。初步说明两种植物提取物可通过影响病原菌的代谢系统和生理过程来发挥其抑菌作用。     

二化螟对杀虫剂抗药性的研究进展

综述了国内外关于二化螟抗药性的研究成果,包括:二化螟的分布、危害、防治,抗药性产生和发展,抗药性机理,抗药性测定方法以及抗药性治理措施。     

4种助剂对异丙隆防除菵草的增效作用

为了比较4种助剂Silwet 806、红太阳A8、激健、安融乐对异丙隆防除菵草Beckmannia syzigachne的增效作用及机制,采用整株生物测定法测定4种助剂与异丙隆混用后对菵草的生物活性及对小麦的安全性;采用仪器分析法测定4种助剂对异丙隆药液的表面张力、叶面接触角、干燥时间和在叶面上的沉积量的影响.结果 表...     

野生稻与栽培稻的杂种后代对褐稻虱的抗性机制初探

为了开拓抗虫基因源,培育抗性稳定的水稻抗虫品种,采用感虫的栽培稻雄性不育株为母本,以高抗褐稻虱的野生稻为父本进行有性杂交。通过用改良的苗期群体筛选法,对其后代进行抗性鉴定,证实其抗性可以遗传,已成功地获得了抗褐稻虱的杂种后代。并根据飞虱在抗虫植株上的生存率、群体建立、蜜露量和稻株的受害级别等指标与感虫对照种TN1上的差异显著性作比较,综合评定杂种后代对褐稻虱的抗性机制。结果表明,测试的N482(A)/101392组合的F_5、F_6、F_7和H_4等几个后代对褐稻虱的抗性机制均为抗生性。     

银胶菊的花对小麦的化感作用机制

采用温室盆栽法,研究了银胶菊的花水浸提液对小麦生长及其生理生化机制的影响,以明确其对小麦的化感作用。结果显示,花水浸提液抑制小麦种子萌发和幼苗生长,且抑制强度随浸提液浓度的升高而加强;随着花水浸提液浓度的增加,小麦叶片光合作用、光合色素含量和过氧化氢酶(CAT)活性下降,磷(P)和丙二醛(MDA)含量升高,氮(N)含量呈现先降低后趋于正常的变化趋势,硝酸还原酶(NR)活性呈现先降低后升高的变化趋势,谷氨酰胺合成酶(GS)活性没有显著变化,而过氧化物酶(POD)和超氧化物歧化酶(SOD)活性则呈现先升高后降低的变化趋势。表明银胶菊的花水浸提液抑制小麦叶片光合作用,提高了小麦叶片的MDA含量,并降低了小麦叶片SOD、POD和CAT的活性。     

苏云金芽孢杆菌营养期杀虫蛋白Vips研究进展

苏云金芽孢杆菌Bt营养期杀虫蛋白Vips主要分为Vip1、Vip2和Vip33种。Vip1和Vip2构成二元毒素,对叶甲科昆虫具有特异杀虫活性。Vip3对鳞翅目昆虫具有广谱杀虫活性,该蛋白广泛存在于Bt中,与已知杀虫晶体蛋白ICPs没有序列相似性。Vip3通过诱发细胞凋亡,最终导致昆虫死亡,这与Btδ-内毒素的作用机理完全不同,Vips的发现对于Bt的进一步开发利用具有重要意义。本文主要对营养期杀虫蛋白Vips的分布、特性、作用机制及应用等进行报道。     

Penetration, Development and Emigration of Juveniles of the Nematode Meloidogyne arenaria in Myrobalan Plum (Prunus cerasifera) Clones Bearing the Ma Resistance Genes

Penetration, development and emigration of M. arenaria in the roots of three Myrobalan plum (Prunus cerasifera) clones genetically characterized for their resistance to root-knot nematodes (RKN) were studied during the 10 (penetration) and 15 (emigration) days following the date of inoculation (D) of 2500 juveniles (J2s) per plant into the soil. Miniaturized tests were conducted on the two resistant clones P.2175 (Ma1 gene) and P.1079 (Ma2 gene) and the susceptible clone P.2032 (recessive for both genes), obtained from micropropagated plantlets and grown in mini-containers under controlled conditions at 25°C in a growth chamber. For penetration and development studies, nematodes in the roots were recovered by the acid fuchsin-lactophenol staining technique. Equivalent numbers of J2s were recovered in all the clones at D+1 and D+2. Subsequently, the numbers increased rapidly in P.2032 and were significantly different from those in P.1079 and P.2175 that remained at a low level. No swollen larvae were observed in the resistant clones. In P.2032, the first swollen larvae were observed at D+4, the first females were observed at D+12, whereas the first females with attached egg sacs and the first new-generation J2s were obtained between D+21 and D+28. Our data suggest that the resistance phenomenon does not act on the very early nematode penetration but acts later by preventing feeding-site induction and development into the third-stage. For emigration studies, plants in which J2s had been allowed to penetrate for two days (from D to D+2) were washed free of soil, repotted and then, after various periods of growth, soil-free roots were placed under a mistifier to evaluate the numbers of emigrating individuals. Emigration of J2s from the roots occured mainly from D+2 to D+4 in all the genotypes and was very limited from D+4 to D+10. There was no significant differences in the number of emigrated juveniles between the resistant and susceptible clones, indicating that emigration cannot explain the difference in the numbers of nematodes recovered in the roots.