植物提取物对黄曲条跳甲成虫毒杀作用的研究

研究24种植物提取物对黄曲条跳甲成虫的毒杀活性。结果表明：处理后72h,供试植物提取物中的7种对黄曲条跳甲成虫有毒杀作用,但毒杀活性较低,其中烟碱对黄曲条跳甲成虫的毒杀效果最好,累积死亡率为3．33％;假莲翘Duranta repeens乙醇提取物对黄曲条跳甲成虫的毒杀效果最差,累积死亡率为1．21％;其余提取物对黄曲条跳甲成虫的毒杀效果居中,累积死亡率为1．67％-2．78％。因此,毒杀作用并不是供试植物提取物对黄曲条跳甲成虫的主要控制机理。     

八种植物提取物对蔬菜害虫的室内毒力研究

研究了巴豆 (Croton tiglium L.)等八种植物的提取物对几种常见蔬菜害虫的非选择性拒食和毒杀作用。研究结果表明 :巴豆、青蒿、米仔兰等三种植物提取物在 0 .5 %浓度时对菜粉蝶 5龄幼虫的拒食率分别达到96 .36 %、82 .4 2 %和 86 .30 % ,对菜粉蝶 3龄幼虫的毒杀死亡率分别为 5 9.38%、2 8.1 3%和 4 3.75 % ;对黄曲条跳甲成虫的毒杀死亡率为 77.5 0 %、5 6 .2 5 %和 4 8.75 % ;对美洲斑潜蝇幼虫的毒杀死亡率分别为 83.33%、5 6 .6 7%和 73.33%。     

马缨丹提取物对黄曲条跳甲成虫的生物活性

测定了马缨丹(Lantana camaraL.)地上部位(茎叶花)的不同溶剂提取物及萃取物对黄曲条跳甲Phyllotreta striolata(Fabricius)成虫的取食忌避、拒食、胃毒和触杀作用。结果表明:处理后48 h,以马缨丹乙醇回流提取物效果最好,其对黄曲条跳甲成虫的取食忌避率达94.94%;非选择性拒食率为85.48%;除正丁醇萃取物对黄曲条跳甲成虫的胃毒作用达到56.67%外,其它处理对黄曲条跳甲成虫的胃毒作用不明显;石油醚萃取物、石油醚冷浸物、乙醇回流物对黄曲条跳甲成虫的触杀作用效果最好,分别为56.67,53.33和53.33%。据实验结果可知马缨丹不同溶剂提取物及萃取物对黄曲条跳甲成虫的生物活性主要表现在对成虫较强的忌避和拒食作用。     

关于黄曲条跳甲的寄主范围

通过非选择性试验方法,测定黄曲条跳甲Ｐｈｙｌｌｏｔｒｅｔａ ｓｔｒｉｏｌａｔａ（Ｆａｂｒｕｃｉｕｓ）在不同植物上的存活率,及番茄、茄子枝叶提取物对曲条跳甲的拒食作用结果表明,在供试的中,仅十字花科植物能使之正常存活,其他科的植物均全部或大量死亡,不可能作为黄曲条跳甲的寄主,甚至茄科的番茄、茄子提取物对黄曲条跳甲在显著的拒食作用,拒食率高达３０．９％和６０．５２％。从化学生态学的角度讨论了典曲条跳甲     

苏云金芽胞杆菌HA和HD对黄曲条跳甲成虫的毒力分析

黄曲条跳甲Phyllotreta striolata (Fabricius)是为害十字花科蔬菜的世界性害虫之一.为了探究苏云金芽胞杆菌HA和HD对黄曲条跳甲成虫的防治潜力,本研究测定了苏云金芽胞杆菌HA和HD菌株对黄曲条跳甲成虫的毒力,以及对其谷胱甘肽-S-转移酶(GST)活性和中肠组织形态的影响.结果 表明:Bt-HA和Bt-HD均对黄曲条跳甲成虫有杀虫活性,LC50分别为4.01×108 CFU/mL和1.17×108 CFU/mL.菌株Bt-HD处理组的GST酶活性高于对照组和菌株Bt-HA处理组.菌株Bt-HA处理黄曲条跳甲成虫14 d后,中肠微绒毛肿胀脱落;菌株Bt-HD处理黄曲条跳甲成虫4d后中肠微绒毛开始疏松脱落,14 d后中肠柱状细胞底膜变形脱落.综上所述,苏云金芽胞杆菌HD对黄曲条跳甲成虫的毒力更强,是防治黄曲条跳甲成虫的优势菌株,其杀虫机理值得深入研究.     

羽裂蟹甲草对家蝇和白纹伊蚊的杀虫活性和活性成分(英文)

为探明羽裂蟹甲草Cacalia tangutica的杀虫活性及其活性成分, 通过拌糖饲喂法和浸渍法测定了羽裂蟹甲草甲醇提取物对家蝇Musca domestica成虫和白纹伊蚊Aedes albopictus 4龄幼虫的毒杀活性, 并采用色谱分离技术和现代波谱技术对羽裂蟹甲草中的化学成分进行了分离鉴定。结果表明： 该植物不同部位甲醇提取物对家蝇成虫和白纹伊蚊4龄幼虫均具有较高的生物活性。从该植物叶和花甲醇提取物中分离鉴定了豆甾醇、 无羁萜、 7 羟基 8 甲氧基香豆素、 7 羟基香豆素、 7, 8 二羟基香豆素、 瑞香素-8-O-β-D-葡萄糖苷、 槲皮素、 山奈酚和β 胡萝卜苷9个化合物。无羁萜、 槲皮素和山奈酚为首次从该植物中分离得到, 500 μg/g拌糖处理48 h后, 其对家蝇成虫的校正死亡率分别为88.30%, 69.90%和77.04%; 50 μg/mL药液处理72 h后, 其对白纹伊蚊4龄幼虫的校正死亡率分别为88.49%, 72.22%和71.06%; 均与鱼藤酮差异不显著（P<0.05）, 表现出良好的杀虫活性。本研究说明羽裂蟹甲草对家蝇和白纹伊蚊具有明显的毒杀活性, 是一种潜在的卫生害虫控制剂。     

马缨丹乳油及其混剂对黄曲条跳甲的拒食活性

测试了自制的12.5%马缨丹乳油对黄曲条跳甲成虫拒食活性、持效性及其与7.5%鱼藤酮乳油、1.5%除虫菊水乳剂、0.3%印楝乳油混配的联合活性。该乳油1000倍液处理菜心叶片后48h对黄曲条跳甲成虫具有40%的拒食率,随着浓度升高,拒食活性增强;200、400和600倍液处理120h后对黄曲条跳甲成虫的累计拒食率分别达到76%、68%和43%。12.5%马缨丹乳油与7.5%鱼藤酮乳油以5∶5比例混配使用时,增效作用最为明显,拒食中浓度AFC50为5.25μg.ml-1,共毒系数CTC为213;与1.5%除虫菊水乳剂以1∶9比例混配使用时的增效作用次之,共毒系数CTC为149;与0.3%印楝乳油以9∶1、7∶3、5∶5、3∶7和1∶9比例混配使用时,其共毒系数CTC均100,表现为相互拮抗作用。结果表明:12.5%马缨丹乳油对黄曲条跳甲成虫具有强烈的拒食活性,其200倍液和400倍液拒食持效性好,且该乳油可与7.5%鱼藤酮乳油混配使用。     

植物精油对土耳其扁谷盗的驱避和熏蒸活性研究

本文研究了34种植物精油对土耳其扁谷盗成虫的驱避和熏蒸毒杀活性。结果表明,肉桂精油对土耳其扁谷盗成虫具有良好的驱避活性,24-48 h内,75%的个体选择了未添加植物精油的小麦;72 h后选择对照组的土耳其扁谷盗成虫降至63.33%,但仍有显著的驱避活性。孜然、松油和黑胡椒精油则对土耳其扁谷盗成虫表现出良好的引诱活性。在34种供试植物精油中,大蒜和芥末精油对土耳其扁谷盗成虫表现出强烈的熏蒸毒杀作用。当植物精油体积分浓度为10μL/L时,这两种植物精油在48 h内对供试害虫的校正死亡率保持在98%以上。进一步的毒力测试结果表明,在24 h、48 h及72 h处理时间下,大蒜精油对土耳其扁谷盗成虫的LC_(50)值分别为0.61、0.59及0.49μL/L,而芥末精油在相同处理时间条件下的LC_(50)值分别为4.35、4.28及4.16μL/L,大蒜精油对土耳其扁谷盗具有更强的熏蒸毒杀活性。     

10种植物乙醇提取物对金银花蚜虫的生物活性研究

采用微量滴定法测定了10种植物乙醇提取物对金银花蚜虫的生物活性.结果表明,10种植物乙醇提取物对金银花蚜虫均有一定的驱避活性和毒杀作用.在10 mg/mL的浓度下,臭椿、曼陀罗和桂花的提取物对金银花蚜虫的驱避作用较强,其在12 h的驱避率分别为78.74％、77.54％、75.11％;夏枯草提取物的驱避效果最弱,12 h的驱避率为58.53％.随着处理时间的延长,各植物提取物的驱避效果均呈下降趋势;印楝提取物的毒杀活性最强,72 h后的校正死亡率达68.30％;曼陀罗和苦瓜的作用次之,72 h后的校正死亡率分别为66.41％和63.70％;夏枯草提取物的作用最低,72 h后的校正死亡率仅为26.47％.进一步的毒力分析表明,印楝提取物对金银花蚜虫的毒力较强,24h的Lc.值为11.0836 mg,/mL.     

薇甘菊五种溶剂提取物对褐稻虱种群的干扰作用

室内测定了薇甘菊（Mikania micrantha）5种溶剂提取物对褐稻虱Nilaparvata lugens Stál种群的干扰作用。结果表明,处理后48h,氯仿提取物和乙醇提取物驱避褐稻虱成虫产卵的作用显著,驱避率分别达86.44%、83.90%;干扰成虫取食效果最好的为乙醇提取物与乙酸乙酯提取物,拒食率分别达74.19%、51.86%;提取物对褐稻虱成虫、若虫具有一定的毒杀活性,其中对1～2龄若虫的活性较强的为乙醇提取物、氯仿提取物和乙醚提取物,对成虫的毒杀活性最强的为乙酸乙酯提取物。综上所述,氯仿提取物和乙醇提取物对褐稻虱实验种群的干扰效果最强,干扰作用控制指数（IIPC）分别达0.0428、0.0515。考虑生物活性、提取效率、溶剂价格与毒性等因素,认为乙醇是一种比较理想的提取杀虫活性成分的有机溶剂。     

Nature and composition of La(III), Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Dy(III) and Ho(III) complexes of embelin

The isolation and characterization of nine polymeric complexes of the general formula [M(L)_1.5S₂]_n (where M is the metal ion, L the ligand and S the solvent, C₂H₅OH) of La(III) and Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III), Ho(III) with.the biologically active compound embelin using elemental and thermal analysis, infrared and electronic spectral studies is reported.     

Physicochemical and biological properties of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose (6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin)

A unique multibranched cyclomaltooligosaccharide (cyclodextrin, CD) of 6(1),6(3),6(5)-tri-O-alpha-maltosyl-cyclomaltoheptaose [6(1),6(3),6(5)-tri-O-alpha-maltosyl-beta-cyclodextrin, (G(2))(3)-betaCD] was prepared. The physicochemical and biological properties of (G(2))(3)-betaCD were determined together with those of monobranched CDs (6-O-alpha-D-glucopyranosyl-alpha-cyclodextrin (G(1)-alphaCD), 6-O-alpha-D-glucopyranosyl-beta-cyclodextrin (G(1)-betaCD), and 6-O-alpha-maltosyl-beta-cyclodextrin (G(2)-betaCD)). NMR spectra of (G(2))(3)-betaCD were measured using various 2D NMR techniques. The solubility of (G(2))(3)-betaCD in water and MeOH-water solutions was extremely high in comparison with nonbranched betaCD and was about the same as that of the other monobranched betaCDs. The formation of an inclusion complex of (G(2))(3)-betaCD with stereoisomers (estradiol, retinoic acid, quinine, citral, and glycyrrhetinic acid) depends on the cis-trans isomers of guest compounds. The cis isomers of estradiol, retinoic acid, and glycyrrhetinic acid were included more than their trans isomers, while the trans isomers of citral and quinine fit more tightly than their cis isomers. (G(2))(3)-betaCD was the most effective host compound in the cis-trans resolution of glycyrrhetinic acid. Among the branched betaCDs, (G(2))(3)-betaCD exhibited the weakest hemolytic activity in human erythrocytes and showed negligible cytotoxicity in Caco-2 cells up to 200 microM. These results indicate unique characteristics of (G(2))(3)-betaCD in some biological responses of cultured cells.     

Synthesis and spectroscopic properties of CpRuCl(R-DAB(4e)) and CpRuCo(CO)3(R-DAB(6e)). Part XVII. X-ray structure determination of CpRuCo(CO)3(t-Bu-DAB(6e))

CpRuCl(PPh₃)₂ reacted with excess R-DAB in refluxing toluene to give CpRuCl(R-DAB(4e)) (1a: R = i-Pr; 1b: R = t-Bu; 1c: R = neo-Pent; 1d: R =p-Tol). ¹H NMR and ¹³C NMR spectroscopic data indicated that in these complexes the R-DAB ligand is bonded in a chelating 4e coordination mode.Reaction of 1a and 1b with one equivalent of [Co(CO)₄]⁻ afforded CpRuCo(CO)₃(R-DAB(6e)) (2a: R = i-Pr; 2b: R = t-Bu). The structure of 2b was determined by a single crystal X-ray structure determination. Crystals of 2b are monoclinic, space group P2₁/n, with four molecules in a unit cell of dimensions: a = 16.812(4), b = 12.233(3), c = 9.938(3) Å and β = 105.47(3)°. The structure was solved via the heavy atom method and refined to R = 0.060 and R_w = 0.065 for the 3706 observed reflections. The molecule contains a RuCo bond of 2.660(3) Å and a cyclopentadienyl group that is η⁵-coordinated to ruthenium [RuC(cyclopentadienyl) = 2.208(3) Å (mean)]. Two carbonyls are terminally coordinated to cobalt (CoC(1) = 1.746(7) and CoC(2) = 1.715(6) Å) while the third is slightly asymmetrically bridging the RuCo bond (RuC(3) = 2.025(6) and CoC(3) = 1.912(6) Å). The RuC(3)O(3) and CoC(3)O(3) angles are 138.4(5)° and 136.5(5)°, respectively. The t-Bu-DAB ligand is in the bridging 6e coordination mode: σ-N coordinated to Ru (RuN(2) = 2.125(4) Å), μ₂-N′ bridging the RuCo bond and η²-CN coordinated to Co (RuN(1) = 2.113(5), CoN(1) = 1.941(4) and CoC(4) = 2.084(5) Å). The η²-CN′ bonded imine group has a bond length of 1.394(7) Å indicating substantial π-backbonding from Co into the anti-bonding orbital of this CN bond.¹H NMR spectroscopy indicated that 2a and 2b are fluxional on the NMR time scale. The fluxionality of 6e bonded R-DAB ligands is rarely observed and may be explained by the reversible interchange of the σ-N and η²-CN′ coordinated imine parts of the R-DAB ligand.     

Structure of Poly (U).poly (A).poly (U)

The molecular structure of poly (U).poly (A).poly (U) has been determined and refined using the continuous x-ray intensity data on layer lines in the diffraction pattern obtained from an oriented fiber of the RNA. The final R-value for the preferred structure is 0.24, far lower than that for the plausible alternatives. The polymer forms an 11-fold right-handed triple-helix of pitch 33.5A and each base triplet is stabilized by Crick-Watson-Hoogsteen hydrogen bonds. The ribose rings in the three strands have C3'-endo, C2'-endo and C2'-endo conformations, respectively. The helix derives additional stability through systematic interchain hydrogen bonds involving ribose hydroxyls and uracil bases. The relatively grooveless cylindrical shape of the triple-helix is consistent with the lack of lateral organization.     

Structure of poly (I).poly (A).poly (I)

The molecular structure of poly (I).poly (A).poly (I) has been determined and refined using the continuous intensity data on layer lines in the x-ray diffraction pattern obtained from an oriented fiber of this polymorphic RNA complex. The polymer forms a 12-fold right-handed triple-helix of pitch 39.7A and each base-triplet is stabilized by quasi Crick-Watson-Hoogsteen hydrogen bonds. The ribose rings in all the three strands have C3'-endo conformations. The final R-value for this best structure is 0.24 and the x-ray fit is significantly superior to all the alternative structures where the different chains might have different furanose conformations. This all-purine triple-helix, counter-intuitively, has a diameter roughly 3A shorter than that of DNA and RNA triple-helices containing a homopurine and two complementary homopyrimidine strands. Its compact, grooveless cylindrical shape is consistent with the lack of lateral organization.     

Structure of poly (dT).poly (dA).poly (dT)

The molecular structure of poly (dT).poly (dA).poly (dT) has been determined and refined using the continuous x-ray intensity data on layer lines in the diffraction pattern obtained from an oriented fiber of the DNA. The final R-value for the preferred structure is 0.29 significantly lower than that for plausible alternatives. The molecule forms a 12-fold right-handed triple-helix of pitch 38.4 A and each base triplet is stabilized by a set of four Crick-Watson-Hoogsteen hydrogen bonds. The deoxyribose rings in all the three strands have C2'-endo conformations. The grooveless cylindrical shape of the triple-helix is consistent with the lack of lateral organization in the fiber.     

The frequencies of Gm(1), Gm(2), Gm(4), Gm(12), and Inv(1) in Hessen (Germany)

Summary The serum groups Gm(1) [Gm(a)], Gm(2) [Gm(x)], Gm(4) [Gm(f)]. Gm(12) [Gm(b)] and Inv(1) [Inv(1)] of 2000 sera of healthy blood donors from the land Hesse were examined. The results obtained were compared with those known until now. Three persons, not related to each other, possessed the extremely rare phenotype Gm(-1, 2, 4, 12) [Gm (a-x+b+f+)]. In 0.75% of the cases we found a discordant behaviour of the factors Gm(4) and Gm(12) [Gm(f) and Gm(b)].

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Zusammenfassung 2000 Seren von gesunden Blutspendern aus Hessen wurden bezüglich der Gamma-Globulin-Serumgruppen Gm(1) [Gm(a)], Gm(2) [Gm(x)], Gm(4) [Gm(f)]. Gm(12) [Gm(b)] und Inv(1) [Inv(1)] untersucht. Die gefundenen Resultate wurden mit den bisher bekannten verglichen. Drei miteinander nicht verwandte Personen wiesen den äußerst seltenen Phänotyp Gm(-1, 2, 4, 12) [Gm(a-x+b+f+)] auf. In 0.75% der Fälle fanden wir ein diskordantes Verhalten der Faktoren Gm(4) und Gm(12) [Gm(f) und Gm(b)].

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Director: Prof. Dr. W. Wachsmuth

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Director: Prof. Dr. W. Spielmann

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The nomenclature suggested by WHO at a round-table conference over genes, genotypes and allotypes of immunglobulins is used. The conference took place in Geneva on the 1965 31. 5. to the 5. 6. [5].

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With technical assistance of S. Mohs.