Absolute configuration of the major sex pheromone component of the satin moth, Leucoma salicis, verified by field trapping test in Hungary

Summary. Male satin moths, Leucoma (Stilpnotia) salicis L. (Lepidoptera, Lymantriidae) were attracted only to (3Z,6R,7S,9R,10S)-isomer out of the four (3Z)-cis-6,7-cis-9,10-diepoxy-3-henicosenes (leucomalure). This was demonstrated by field trapping test with a bivoltine population in a mixed poplar-willow forest along the flood area of the river Danube at Adony, Hungary.     

Antifungal activity of a flavonol glycoside from the leaves of bog myrtle (Myrica gale)

Summary The antifungal activity of kaempferol-3-(2,3-diacetoxy-4-p-coumaroyl)rhamnoside, a new flavonol glycoside isolated from the leaves ofMyrica gale, has been investigated. The flavonoid was found to have varying inhibitory activity against five species of fungi isolated from the leaves ofMyrica gale in the field.     

水体中胺鲜酯残留量的测定及其光解特性

建立了利用固相萃取-气相色谱(SPE-GC)测定水体中胺鲜酯残留量的方法.考查了3种不同固相萃取柱(C18、florisil、OasisR HLB)对水溶性农药胺鲜酯的吸附效果,发现它们对水中胺鲜酯的萃取效率依次为8%、13% 和96%;进一步研究了利用OasisR HLB萃取水中胺鲜酯的最佳条件(洗脱剂二氯甲烷用量4～8 mL),OasisR HLB(60 mg)小柱对胺鲜酯的保留容量高达200 μg·柱-1.运用该方法测定胺鲜酯光解试验样品,结果表明胺鲜酯质量浓度的对数与光照时间呈良好的线性关系.胺鲜酯在氙灯下的光化学降解符合一级动力学反应,光解半衰期为82 min,较易光解.     

How <Emphasis Type="Italic">Doratomyces stemonitis</Emphasis> copes with Benzoxazolin-2(3<Emphasis Type="Italic">H</Emphasis>)-one (BOA), its derivatives and detoxification products

Summary. Doratomyces stemonitis (Hyphomycetales, Dematiaceae) is a saprotrophic fungus belonging to the mycobiota of the cereal rhizosphere. The fungus is able to metabolize benzoxazolin-2-(3H)-one and a variety of its derivatives including higher plant detoxification products, microbial degradation products and the chemically rather stable 2-amino-(3H)-phenoxazin-3-one. D. stemonitis can use all of these compounds as sole C-sources but their utilization, especially that of microbial degradation products and 2-amino-(3H)-phenoxazin-3-one, seems to be highly energy consuming, resulting in slow mycelium growth and a change of colony morphology. Benzoxazolin-2-(3H)-one derived compounds induce the synthesis of different isoforms of a glycosylated protein with sequence homologies to the endo-1,3-β-glucanase Asp f2, an allergen from Aspergillus fumigatus and other Asp f2-like proteins e.g., from Verticillium dahliae or PRA1 antigen from Candida albicans. The induction of the protein is regarded as a stress response.     

Oviposition stimulants for the pipevine swallowtail butterfly,Battus philenor (Papilionidae), from anAristolochia host plant: Synergism between inositols,aristolochic acids and a monogalactosyl diglyceride

Aristolochia macrophylla (Lam.) is a major host of the pipevine swallowtail butterfly,Battus philenor (L.), in the eastern United States. The female butterflies use a synergistic mixture of inositols, acids and a lipid as oviposition cues in recognizing this plant on contact. The acids and lipid, all isolated from the Et₂O-CHCl₃ fraction of an alcoholic extract of fresh foliage, were identified as aristolochic acid I (1), aristolochic acid II (2) and 1,2-[di(9Z,12Z,15Z)-octadeca-9, 12, 15-trienoyl]-3-galactosyl-sn-glycerol (3). Identifications were facilitated by UV, MS (EI and FAB) and NMR (1D and 2D) spectral techniques and by analysis of the hydrolysis products of 3. The active inositols were identified as D-(+)-pinitol, reported previously, and sequoyitol. Though this is apparently the first report of oviposition responses to a diacyl glycerol glycoside by a phytophagous insect, responses to aristolochic acids and sequoyitol have been reported previously for anAristolochia-feeding swallowtail of a different genus in Japan. This indicates substantial evolutionary conservatism in chemical oviposition cues within the tribe Troidini.     

Terminal double bonds in the alkenes and acetates of defensive secretion from the thrips Suocerathrips linguis Mound & Marullo, 1994 (Thysanoptera: Phlaeothripidae)

Defensive secretions of adult males and females of the subsocial thrips Suocerathrips linguis were examined using gas chromatography–mass spectrometry (GC–MS). The samples contained six long-chain acetates and five aliphatic alkanes and alkenes. Whole-body extracts yielded six methyl esters of fatty acids as well as hexadecyl acetate. Structures of the two main components, (11Z)-icosa-11,19-dienyl acetate and octadecyl acetate, were confirmed. The third most abundant substance was identified as octadec-17-enyl acetate, which is a new natural product. In addition, (9Z)-octadec-9-enyl acetate was identified along with other acetates. Pure icosadienyl acetate was found to remain liquid down to −15°C, and is the solvent for the solid components of the secretion cocktail. A tentative biosynthetic pathway for all of the 12 acetates, alkanes and alkenes is discussed, considering especially the components with terminal double bonds that are uncommon in Thysanoptera and other insects.