Sex Pheromone of Callosobruchus subinnotatus

Sex pheromone produced by Callosobruchus subinnotatus females stimulates conspecific males to walk upwind toward the source. Gas chromatographic and mass spectrometric analyses of sex pheromone components and their hydrogenated derivatives suggested that the sex pheromone consisted of two short-chain fatty acids, (E)-3-methyl-2-heptenoic acid (E32C7) and (Z)-3-methyl-2-heptenoic acid (Z32C7). The composition of the sex pheromone was confirmed by electrophysiological and behavioral bioassays with synthetic compounds. A mixture of 5 ng E32C7 and 5 ng Z32C7 elicited a 2.1-mV male EAG response, whereas the solvent control elicited 0.1 mV. Mixtures of the two compounds at various ratios were attractive to males in Y-tube bioassays. A pitfall-type trap equipped with a lure impregnated with 1 ng E32C7 and 1 ng Z32C7 was effective in trapping males. Traps baited with the lure caught 80% of males in a glass aquarium during nighttime and 50% during daytime, whereas control traps (solvent treated) in a separate aquarium caught 20% and 10%, respectively.     

A Male Sex Pheromone in a Scorpionfly

It has been postulated that males of a number of scorpionfly species produce sex pheromones. This is based on the observation that females often respond only to conspecific males when they evert their genital pouch, the proposed site of pheromone release. In this study, we prove that in Panorpa germanica (Mecoptera, Panorpidae), the eversion of a male’s genital pouch is associated with the release of a volatile sex pheromone. In dual choice situations, females showed a high preference for ‘calling’ (males with everted genital pouch) over noncalling individuals. Volatiles emitted by males and females were collected and identified by coupled gas chromatography–mass spectrometry. Two aldehydes [(2E,6Z)-nona-2,6-dienal and (E)-non-2-enal] were characteristic of calling males but not of noncalling or immature males or females. Bioassays with synthetic compounds confirmed that the identified substances are attractive to females. To the best of our knowledge, this is the first identification of a sex pheromone in scorpionflies.     

粉蚧虫性信息素的研究进展

粉蚧虫性信息素是一种重要绿色杀虫剂,与常规的杀虫剂相比具有专一性、无毒、高效、不伤害天敌等优点,近年来受到普遍的关注.叙述了近期发现的粉蚧虫性信息素及其鉴定出的结构,同时介绍了部分粉蚧虫性信息素的合成路线.最后论述了粉蚧虫性信息素的研究现状及在国内外的发展前景.     

Identification of the Sex Pheromone of Holotrichia reynaudi

The male attractant pheromone of the scarab beetle Holotrichia reynaudi, an agricultural pest native to southern India, was extracted from abdominal glands of females with hexane and analyzed by gas chromatography–mass spectrometry. Field testing of the candidate chemicals, indole, phenol, and anisole, both alone and as binary mixtures, led us to conclude that anisole was the major component of the sex pheromone. Neither male nor female beetles were attracted to indole or phenol on their own. Similarly, when indole and anisole were combined, the attractiveness of the solution did not increase over that obtained with anisole alone. However, combination of phenol and anisole did alter the attractiveness of anisole, with fewer male beetles attracted to the binary mixture than to anisole on its own. The behavior of female beetles was not altered by any of the chemicals tested. Anisole is also the sex pheromone of H. consanguinea, making this the first known example of two melolonthine scarabs sharing the same pheromone.     

Sex Pheromone of the Mirid Bug Phytocoris relativus

The sex attractant pheromone produced by adult females of the mirid bug Phytocoris retativus has been identified as a 2:1 blend of hexyl acetate with (E)-2-octenyl butyrate. The pheromone is stage-, sex-, and species-specific, attracting only adult male P. relativus. Hexyl acetate was identified in aeration extracts from both sexes, while (E)-2-octenyl butyrate was produced only by females. Both males and females also produced hexyl butyrate and octyl acetate, while only females produced (E)-2-hexenyl and octenyl acetates, and (Z)-3-octenyl acetate. The function(s) of these chemicals were not determined. Attraction of males increased with dose, with doses of 0.1 to 33 mg loaded on grey rubber septa. Attractiveness of rubber septum lures decreased quickly with age due to the volatility of the two pheromone components.     

Sex Attractant Pheromone of Saturniid Moth Coloradia velda

The female-produced sex attractant pheromone of Coloradia velda has been identified by a combination of analytical methods and field tests as a blend of (10E,12Z)-hexadecadien-1-yl acetate (10E,12Z–16:Ac), (10E,12E)-hexadecadien-1-yl acetate (10E,12E–16:Ac), and (10E,12Z)-hexadecadien-1-ol (10E,12Z–16:OH) in a 10:1:0.33 ratio, respectively. The corresponding aldehyde (10E,12Z–16:Ald) was also found in extracts of female pheromone glands, but in blends with 10E,12Z–16:Ac and 10E,12E–16:Ac at low doses did not significantly increase the attractiveness of baits to male moths.     

Identification of a Sex Pheromone Component of Pseudococcus cryptus

A sex pheromone component of Pseudococcus cryptus has been isolated and identified. The crude pheromone extract obtained by airborne collection was fractionated by liquid chromatography (LC) on Florisil, and further purified by high performance liquid chromatography and preparative Gas Chromatography (GC). The pheromone component was shown to be an ester, the alcohol part of which was identical to the known alcohol moiety of the pheromone of Planococcus citri. The chemical structure was determined to be 3-isopropenyl-2,2-dimethylcyclobutylmethyl 3-methyl-3-butenoate by MS and ¹H NMR analyses. The absolute configuration of the pheromone was assigned as (1R,3R) by comparison of the retention time of the alcohol derived from the P. cryptus pheromone with those of the alcohol derived from P. citri pheromone, and a synthetic sample of alcohol enriched in the (1R,3R)-enantiomer, using a chiral GC stationary phase. The structure of the pheromone was confirmed by synthesis, and by bioassays in a glasshouse.     

Identification of the Sex Pheromone of Sesamia cretica Lederer

By using solid phase micro-extraction and gas chromatography–mass spectrometry analyses, a sex pheromone blend for the stem borer, Sesamia cretica Lederer (Lepidoptera, Noctuidae), was identified as consisting of (Z)-9-tetradecen-1-ol (80%), (Z)-9-tetradecen-1-yl acetate (10%), and (Z)-11-hexadecen-1-ol (10%). The first two components had previously been discovered as attractants for S. cretica in field tests, but had not been identified in the female’s sex pheromone gland. A field-trapping trial showed that the three-component blend gave the highest catches of male S. cretica. This blend, in a sticky trap, was used to monitor a population of S. cretica in Iran, allowing the seasonal flight activity of this insect to be compared with that of a sympatric population of S. nonagrioides. The role of pheromones in the reproductive isolation of these species is discussed.     

梨小食心虫性信息素的简便合成

[目的]以廉价、易得的原料合成梨小食心虫性信息素(Z/E)-12-十四碳烯醇乙酸酯.[结果]以35.9%的总收率合成了梨小食心虫性信息索(Z/E)-12-十四碳烯醇乙酸酯,GC分析结果表明顺反异构体比例为87/13.将所得的顺反异构体混合物在亚硝酸钠和硝酸体系中经构型转化得到顺反比例为23/77的(Z/E)-12-十四碳烯醇乙酸酯,产物结构经IR、1H NMR等方法确证.[结论]该路线简洁且比大多数文献报道的方法产率略高,值得借鉴.     

梨小食心虫性信息素的合成进展

综述了梨小食虫性信息素合成方法的进展。     

Sex Pheromone Components of Nettle Caterpillar, Setora nitens

Gas chromatographic–electroantennographic detection (GC-EAD) analyses of pheromone gland extracts of female nettle caterpillars, Setora nitens, revealed four compounds that consistently elicited responses from male moth antennae. Retention indices on three fused silia columns (DB-5, DB-23, and DB-210) of two EAD-active compounds were almost identical to those of (E)-9-dodecenal (E9–12 : Ald) and (E)-9,11-dodecadienal (E9,11–12 : Ald), two pheromone components previously identified in congeneric Setothosea asigna. However, comparative GC, GC-EAD, and GC-mass spectrometry of extracted S. nitens compounds and authentic standards revealed that the candidate pheromone components were (Z)-9-dodecenal (Z9–12 : Ald) and (Z)-9,11-dodecadienal (Z9,11–12 : Ald). The two other EAD-active compounds in pheromone gland extracts proved to be the corresponding alcohols to these aldehydes. In field-trapping experiments in Tawau, Malaysia, synthetic Z9–12 : Ald and Z9,11–12 : Ald at a 1 : 1 ratio, but not singly, attracted male S. nitens. Attractiveness of these two aldehydes could not be enhanced through the addition of their corresponding alcohols. Whether these differences in pheromone biology and chemistry between S. nitens and S. asigna are sufficient to prevent cross-attraction of heterospecific males or whether nonpheromonal mechanisms are required to maintain reproductive isolation is currently being studied.     

Female-Produced Sex Pheromone of the Predatory Bug Geocoris punctipes

A compound identified from air-entrained volatiles produced by adult female Geocoris punctipes attracted male bugs and stimulated males to investigate nearby moving objects of the appropriate size in their search for females. The compound was identified as (E)-2-octenyl acetate, a relatively common component of the volatile semiochemicals produced by a number of heteropteran species. This compound comprised a significant proportion of the female volatiles, whereas it was detected in only trace amounts in volatiles collected from live males. Other components in the extracts from adults of both sexes included (E)-2-hexenyl acetate, (E)-2-octenal, and several saturated hydrocarbons, but these components were not part of the attractant. These compounds plus (E)-2-hexenal, (E)-4-oxo-2-hexenal, and (E)-2-decenal were found in extracts of homogenized adults, whereas the cast skins from late instar nymphs contained (E)-2-octenal, (E)-4-oxo-2-octenal, (E)-2-octenoic acid, and several saturated hydrocarbons.     

Male-Produced Sex Pheromone of the Stink Bug Edessa meditabunda

Edessa meditabunda is a secondary pest within the piercing-sucking stink bug complex that attacks soybean crops in Brazil. The behavioral responses of males and females to aeration extracts from conspecifics suggested the presence of a male-produced sex pheromone. Gas chromatographic (GC) analysis of male and female aeration extracts revealed the presence of two male-specific compounds in a ratio of 92:8. Gas chromatographic -electroantennographic detection (GC-EAD) assays indicated that the major component is bioactive for females, supporting the behavioral data. Analysis of the mass and infrared spectra of the male-specific compounds suggested that they were both methyl-branched long-chain methyl esters. On the basis of the mass spectra of the respective hydrocarbons obtained by micro derivatizations, the structures of these methyl esters were proposed to be methyl 4,8,12-trimethylpentadecanoate (major) and methyl 4,8,12-trimethyltetradecanoate (minor). An 11 step synthetic route that was based on a sequence of Grignard reactions, starting from cyclopropyl methyl ketone, was developed to obtain synthetic standards with a 7.9 % overall yield for the major compound and a 9.9 % yield for the minor. The synthetic standards co-eluted with the natural pheromones on three different GC stationary phases. Y-tube olfactometer assays showed that the synthetic standards, including the major compound alone and a mixture of the major and minor compounds in the proportion found in natural extracts, were strongly attractive to females.     

Sex Pheromone of the Cranberry Root Grub Lichnanthe vulpina

The cranberry root grub Lichnanthe vulpina (Hentz) (Coleoptera: Glaphyridae) is a pest of cranberries in Massachusetts, reducing yield and vine density. (Z)-7-Hexadecenol and (Z)-7-hexadecenal were identified from the female effluvia collection by gas chromatographic–electroantennographic detection and gas chromatography–mass spectrometry. The double-bond position was confirmed by dimethyl disulfide derivatization. Both compounds were tested in the field, each alone and as blends of the two. Each compound alone captured males; however, (Z)-7-hexadecenol alone captured significantly more males than did (Z)-7-hexadecenal alone. The addition of varying amounts of (Z)-7-hexadecenal to (Z)-7-hexadecenol did not statistically affect male capture. Flight activity of the cranberry root grub may be monitored with traps baited with rubber septa containing 300 μg of (Z)-7-hexadecenol. A test of trap vane colors indicated that traps with green or black vanes maximized target male catch while minimizing nontarget catch of important cranberry pollinators. ^*Deceased May 15, 2001. He is dearly missed by his family, friends, and colleagues.     

Sex Pheromone Components of Casuarina Moth, Lymantria xylina

cis-7,8-Epoxy-2-methyleicosane is a sex pheromone component of the Casuarina moth, Lymantria xylina Swinhoe. The compound was extracted from pheromone glands of female moths and was identified by coupled gas chromatographic–electroantennographic detection (GC-EAD) and GC–mass spectrometry. In field experiments in Taiwan, traps baited with either or both of (7R,8S)-cis-7,8-epoxy-2-methyleicosane (>99% ee) [termed here (+)-xylinalure] and (7S,8R)-cis-7,8-epoxy-2-methyleicosane (>99% ee) [termed here (–)-xylinalure] captured male L. xylina. Addition of further candidate pheromone components to xylinalure did not enhance its attractiveness. Demonstration of whether or not female L. xylina produce both optical isomers of xylinalure, and determination of the ratio, will require pheromone extract analyses on a chiral, enantiomer-separating column (as yet unavailable) or derivatization of epoxides in accumulated gland extracts. Attraction of male L. xylina to either enantiomer of xylinalure contrasts with enantiospecific production of, and/or response to, epoxy pheromones in congeners. With no other nocturnal lymantriid moth known in Taiwan to utilize xylinalure for pheromonal communication, enantiospecific fine tuning of xylinalure, or evolution of a more complex pheromone blend, may not have been necessary for L. xylina to maintain specificity of sexual communication. Racemic xylinalure will be appropriate for pheromone-based detection surveys of L. xylina in North America.     

鳞翅目斑蛾科昆虫性信息素的合成

鳞翅目斑蛾科昆虫为森林和果树的重要害虫,可利用昆虫性信息素进行斑蛾科害虫的种群预测和直接诱杀.以7-溴庚酸为起始原料,经过二氯亚砜酰氯化、仲丁醇酯化得到7-溴庚酸仲丁醇酯,再与三苯基膦反应得到膦盐,最后与正戊醛进行相转移催化的Wittig反应,合成了鳞翅目斑蛾科昆虫性信息素顺-7-十二碳烯酸仲丁醇酯(Z7-12:COO...     

Sex Pheromone of South American Tortricid Moth Argyrotaenia sphaleropa

By means of electroantennographic detection and gas chromatography-mass spectrometry, the sex pheromone of Argyrotaenia sphaleropa was identified as a mixture of (Z)-11-tetradecenal, (Z)-11,13-tetradecadienal, (Z)-11-tetradecenyl acetate, and (Z)-11,13-tetradecadienyl acetate in the ratio of 1:4:10:40. Best trap catches were obtained with mixtures of (Z)-11-tetradecenal and (Z)-11,13-tetradecadienal in the ratio of 1:4 to 1:9.     

Male-Released Sex Pheromone of the Stink Bug Piezodorus hybneri

Male-released semiochemicals of the stink bug Piezodorus hybneri (Heteroptera: Pentatomidae) elicit attraction of male and female bugs and homosexual behavior in males. Three active components were isolated from the airborne volatiles of males by flash chromatography, with the activity monitored by GC-EAD and behavioral bioassay. The pheromone system was characterized as a mixture of -sesquiphellandrene, (R)-15-hexadecanolide, and methyl 8-(Z)-hexadecenoate (ratio: 10:4:1), and the activity of the semiochemicals was assessed with authentic samples. Enantiomerically pure samples of the R and S macrolactones were obtained by Yamaguchi's and Mitsunobu's macrolactonization of a key intermediate, (R)-15-hydroxyhexadecanoic acid. The nonnatural S stereoisomer was neither a beneficial nor a behavioral antagonist. Individual constituents or binary mixtures were active, but the optimal male response was elicited only by the full mixture. Behavioral observation and the fact that the onset of pheromone production is coincident with ovarian development strongly suggest that these semiochemicals are, in fact, sex pheromones.     

松树叶蜂性信息素中间体的合成研究

:3,7 二甲基 2 十三醇是松树叶蜂Diprionpini性信息素的前体化合物。设计并研究了一条新的 3,7 二甲基 2 十三醇的合成路线 ,并对该路线中两个重要的中间体 2 甲基 1 溴辛烷和 3 甲基 4,4 [1′,2′ 丙二氧基 2 戊酮进行了合成研究。丙二酸二乙酯经己基化、甲基化、水解、脱羧、还原、溴化得到 2 甲基 1 溴辛烷 ,单程总收率为 2 8 4%。 2 ,4 戊二酮经甲基化、单羰基保护得到3 甲基 4,4 (1′ ,2′ 丙二氧基 ) 2 戊酮 ,单程总收率为 15 0 %     

松叶蜂性信息素中间体的合成

对类欧松叶蜂(Diprionsimiles)和红头新松叶蜂(Neodiprionlecontei)性信息素前体化合物———(2S,3S,7S) 3,7 二甲基 2 十五碳醇的合成进行了设计和研究,重点对其中的两个中间体(2S,3S) 2 甲基 3 苄氧基丁醛和(S) 3 甲基十一碳 6 烯醇进行了合成。以顺 2 丁烯为原料,经Browncrotylation反应,得到(2S,3S) 3 甲基戊 4 烯 2 醇,该化合物羟基经苄基保护,所得产物于室温下依次进行OsO4氧化、NaIO4氧化,合成了(2S,3S) 2 甲基 3 苄氧基丁醛,总收率为56 3%。(S) 香茅醇经羟基保护、OsO4氧化、NaIO4氧化、Wittig反应、脱保护等反应,于室温条件下合成了(S) 3 甲基十一碳 6 烯醇,总收率为40 0%。为此种松叶蜂性信息素的全合成奠定了基础。