Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1570-7458
    Keywords: sex pheromone ; lima-bean pod borer ; Etiella zinckenella ; Lepidoptera ; Phycitidae ; (Z)-11-tetradecenyl acetate ; (E)-11-tetradecenyl acetate ; (Z)-9-tetradecenyl acetate ; tetradecyl acetate ; Hungary ; Egypt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Résumé A partir de femelles d'E. zinckenella d'origines hongroise et égyptienne, nous avons isolé quatre composés par chromatographie en phase gazeuse avec ionisation de flamme et électroantennographie (EAD): l'acétate de tétradécanyl, l'acétate (Z)-11-tétradécényl, l'acétate (E)-11-tétradécényl et l'acétate (Z)-11-tétradécényl. Les acétates monoinsaturés donnent les meilleures réponses en EAG parmi une série d'acétates tétradécényls et de tétradécénols. Les quatre composés mélangés dans les mêmes proportions que dans l'extrait de la phéromone ont attiré un nombre significatif de mâles tant en Egypte qu'en Hongrie. Dans un test préliminaire de soustraction, la meilleure capture a été réalisée par le mélange ternaire d'acétates monoinsaturés.
    Notes: Abstract Four compounds, tetradecyl acetate, (Z)-9-tetradecenyl acetate, (E)-11-tetradecenyl acetate and (Z)-11-tetradecenyl acetate were identified from female sex pheromone extracts of Hungarian and Egyptian lima-bean pod borers (Etiella zinckenella Tr., Lepidoptera: Phycitidae) by gas chromatography with flame ionization (FID) and electroantennographic (EAD) detection. In EAG studies these monoun-saturated acetates gave the best responses in a series of other tetradecenyl acetates and tetradecenols. The four component blend of the identified components in similar ratios as in the pheromone extract attracted significant numbers of male lima-bean pod borers in both Hungary and Egypt. In a preliminary subtraction test best capture was achieved by the ternary mixture of the monounsaturated acetates.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1570-7458
    Keywords: (E,Z)-2,13-octadecadien-1-ol acetate ; (E,Z)-3,13-octadecadien-1-ol acetate ; Synanthedon tipuliformis ; Sesiidae ; Lepidoptera ; field trapping ; sex attractant ; geographical differences ; Belgium ; Bulgaria ; Denmark ; GDR ; Hungary ; Italy ; Lithuania ; Norway ; Soviet Union ; Switzerland ; United Kingdom
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Entomologia experimentalis et applicata 61 (1991), S. 95-96 
    ISSN: 1570-7458
    Keywords: Swammerdamia pyrella ; Lepidoptera ; Yponomeutidae ; (Z)-5-tetradecenyl acetate ; (Z)-7-tetradecenyl acetate ; sex attractant ; field trapping
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1573-1561
    Keywords: Mountain-ash bentwing ; Leucoptera scitella ; Lepidoptera ; Lyonetidae ; (R,R)-5,9-dimethylheptadecane ; (R,S)-5,9-dimethylheptadecane ; (S,R)-5,9-dimethylheptadecane ; (S,S)-5,9-dimethylheptadecane ; 5,9-dimethylhexadecane ; trapping ; behavior ; sex pheromone ; asymmetric synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Among the pure stereoisomers of 5,9-dimethylheptadecane, a previously identified sex pheromone component ofLeucoptera scitella L., only theS,S isomer yielded trap captures in the field. The addition of the other stereoisomers had no effect on cathes. The addition of low percentages of racemic 5,9-dimethylhexadecane, a previously identified minor component in the sex pheromone, did not influence trap catches or alter behavior of males approaching an attractant source in the field.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1573-1561
    Keywords: Currant borer ; Synanthedon tipuliformis ; Lepidoptera ; Sesiidae ; (E,Z)-2,13-octadecadien-1-ol acetate ; (E,Z)-3,13-octadecadien-1-ol acetate ; (Z,Z)-3,13-octadecadien-1-ol acetate ; sex pheromone ; trapping synergist ; trapping inhibitor ; field trapping ; sexual behavior ; geographically isolated populations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Various blends of (E,Z)-2,13-octadecadien-1-ol acetate (E,Z2,13-18: OAc), (Z)-13-octadecen-1-ol acetate (ZOAc) (two previously identified pheromone components of the currant borer,Synanthedon tipuliformis females), (E,Z)-, (Z,Z)-3,13-octadecadien-1-ol acetates (E,Z- andZ,Z3,13–18:OAc), andZ,Z-3,13-octadecadien-1-ol (Z,Z3,13–18:OH) were evaluated in field traps in three geographic regions. MaleS. tipuliformis were attracted toE,Z2,13–18:OAc in Tasmania, New Zealand, and Hungary. Captures were not influenced by the addition ofZ13–18: OAc, tested in Tasmania and Hungary. In Hungary and New Zealand, the addition ofE,Z3,13–18: OAc toE,Z2,13–18:OAc in a ratio of 100:3 was strongly synergistic; however, in Tasmania captures were reduced. The addition ofZ,Z3,13–18: OAc toE,Z2,13–18:OAc in a ratio of 10∶1 resulted in strong inhibition of trap captures in Hungary. WhenZ,Z3,13–18: OAc was added in different ratios to a 100:3 binary mixture ofE,Z2,13–18:OAc/E,Z3,13–18:OAc in Hungary, it strongly reduced captures at, or above a ratio of 100∶3∶3 but no decrease was recorded at a ratio of 100∶3∶1. In New Zealand and Tasmania it reduced captures at a ratio of 100∶3∶1. Observations of behavioral responses of maleS. tipuliformis in Hungary to synthetic baits in the field showed thatE,Z2,13–18:OAcby itself evoked close-range approaches to the source from only 20% of males, whereas the addition ofE,Z3,13–18:OAc in a ratio of 100∶3 raised that value to 65 %. Landing on the source was significant only at sources with a 100∶3∶0.1∶3∶10 blend ofE,Z2,13–18:OAc/E,Z3,13–18: OAc/Z,Z3,13–18: OAc/Z,Z3,13–18: OH/Z13–18: OAc. A 100∶3 binary mixture ofE,Z2,13–18:OAc/E,Z3,13–18:OAc in a dose range of 10–1000 μg can be recommended for more effective field monitoring ofS. tipuliformis populations in Hungary and in New Zealand. In Tasmania, at present,E,Z2,13–18: OAc by itself is the most potent sex attractant of the species.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    ISSN: 1573-1561
    Keywords: Pheromone identification ; (6Z,9Z)-6,9-cis-3,4-epoxyhepta-decadiene ; (3Z,6Z,9Z)-3,6,9-heptadecatriene ; Abraxas grossulariata ; Lepidoptera ; Geometridae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract (3Z,6Z,9Z)-3,6,9-Heptadecatriene and (6Z,9Z)-6,9-cis-3,4-epoxyheptadecadiene have been identified in female sex pheromone gland extracts ofAbraxas grossulariata L. (Lepidoptera: Geometridae). The compounds were detected by gas chromatography with electroantennographic detection (GC-EAD) and identified by GC-mass spectrometry (GC-MS). The amounts of hydrocarbon and epoxide were 0.13 and 0.42 ng/female, respectively. These identifications were confirmed by synthesis; the absolute configuration of the epoxide remains to be determined. Another isomeric epoxide, (3Z,6Z)-3,6-cis-9,10-epoxyheptadecadiene, was tentatively identified in small amounts (0.04 ng/female). Racemic (6Z,9Z)-6,9-cis-3,4-epoxyheptadecadiene elicited the largest electroantennogram response within a series of heptadecadiene and nonadecadiene monoepoxides and the corresponding trienic hydrocarbons and, in field tests, attracted maleA. grossulariata into traps. Addition of 10% (3Z,6Z,9Z)-3,6,9-heptadecatriene to this epoxide enhanced attractiveness; addition of (3Z,6Z)-3,6-cis-9,10-epoxyheptadecadiene had no effect at low proportions while higher proportions caused a reduction in the numbers of males caught.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1573-1561
    Keywords: Chirality ; enantiomers ; sex pheromones ; (3Z,9Z)-(6R,7S)-epoxynonadecadiene ; (3Z,9Z)-(6S,7R)-epoxynonadecadiene ; (6Z,9Z)-(3S,4R)-epoxynonadecadiene ; Colotois pennaria ; Erannis defoliaria ; Agriopis aurantiaria ; A. marginaria ; A. leucophearia ; Lepidoptera ; Geometridae ; electroantennogram ; field trapping
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Enantiomer separation of (6Z,9Z)-cis-3,4-epoxynonadecadiene and (3Z,9Z)-cis-6,7-epoxynonadecadiene could be achieved using chiral high-resolution gas chromatography and a cyclodextrin-bond column. (3Z,9Z)-(6R,7S)-Epoxynonadecadiene was identified from ovipositor extracts ofColotois pen-Naria, while inErannis defoliaria the 6S,7R-enantiomer was found. In field trapping tests pure synthetic enantiomers caught only conspecific males of these species. (3Z,6Z,9Z)-Nonadecatriene was found in both species, while the presence of (3Z,6Z,9Z)-heneicosatriene was indicated inC. Pennaria only. A 10∶10∶3 blend of (3Z,9Z)-(6R,7S)-epoxynonadecadiene, (3Z,6Z,9Z)-heneicosatriene, and (3Z,6Z,9Z)-nonadecatriene was found to be optimal for catchingC. Pennaria, whileE. Defoliaria males were optimally caught by a 1∶1 mixture of (3Z,9Z)-(6S,7R)-epoxynonadecadiene and (3Z,6Z,9Z)-nona-decatriene. (6Z,9Z)-(3S,4R)-Epoxynonadecadiene was identified from ovipositor extracts ofAgriopis (Erannis) aurantiaria. In field tests the pure enantiomer proved to be a highly specific sex attractant for both the late autumn/early winter flyingA. Aurantiaria and the late winter/early spring flyingA. Leucophearia. Males ofAgriopis marginaria, which fly in late winter/early spring, were attracted to (3Z,9Z)-(6S,7R)-epoxynonadecadiene. The addition of (3Z,6Z,9Z)-nonadecatriene to theS,R-enantiomer increased captures. Optimal catches were recorded with a 10∶3 epoxide-hydrocarbon blend. Enantiomer specificity in all species was confirmed in EAG measurements.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...