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  • pheromone  (4)
  • Springer  (4)
  • International Union of Crystallography
  • PANGAEA
  • 2000-2004
  • 1975-1979  (4)
  • 1960-1964
  • 1945-1949
  • 1935-1939
  • 1978  (2)
  • 1976  (2)
Collection
Publisher
  • Springer  (4)
  • International Union of Crystallography
  • PANGAEA
Years
  • 2000-2004
  • 1975-1979  (4)
  • 1960-1964
  • 1945-1949
  • 1935-1939
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 2 (1976), S. 187-193 
    ISSN: 1573-1561
    Keywords: Malacosoma americanum ; tent caterpillar ; chemical trail substance ; pheromone ; trail-following behavior
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The leaf-feeding larvae of the eastern tent caterpillarMalacosoma americanum (Fabricius) follow silk trails laid down on branches leading from their communal tent to distant foraging sites. The response of colonies reared in the laboratory under seminatural conditions to silk trails washed in methylene chloride and to chemical trails prepared from a solvent extract of their tent or trail silk, showed that one or more soluble components of their trail is essential to the elicitation of the following response. The demonstrated ability of the caterpillars to distinguish between old and newly reinforced silk trails most likely occurs in response to a temporal change in the detectable chemical properties of their trail.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 4 (1978), S. 211-224 
    ISSN: 1573-1561
    Keywords: California red scale ; Aonidiella aurantii ; pheromone ; attractant ; enantiomer ; isomers (E,Z)-3-methyl-6-isopropenyl-9-decen-1-yl acetate ; (Z)-3-methyl-6-isopropenyl-3,9-decadien-1-yl acetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Pheromone components of female California red scale,Aonidiella aurantii (Maskell) were isolated from airborne collections and found to be 3-methyl-6-isopropenyl-9-decen-1-yl acetate and (Z)-3-methyl-6-isopropenyl-3,9-decadien-1-yl acetate. Both enantiomers of the latter compound as well as the corresponding enantiomers of theE isomer were prepared from (S)- or (R)-carvone. Bioassays with each of the four isomers showed that only theR,Z isomer attracted male red scale.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-1561
    Keywords: Spruce budworm ; Choristoneura fumiferana ; pheromone ; female behavior ; electroantennogram ; dispersal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Female eastern spruce budworm moths respond to the synthetic sex pheromone of their own species (a mixture ofcis- andtrans-11-tetradecenal) by walking, antennal grooming, flexation of the body, extension of the ovipositors, and oviposition. The sex pheromone is perceived by receptors on the antennae. Electroantennogram responses from the female are approximately two-thirds the amplitude of those obtained from males.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-1561
    Keywords: carpenterworm moth ; Prionoxystus robiniae ; (Z,E)-3,5-tetradecadien-1-ol acetate ; pheromone ; electroantennogram
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Electroantennogram analyses of female gland extract and of male antennal responses to synthetic standards suggested that (Z,E)-3,5-tetradecadien-1-ol acetate is a pheromone component for the carpenterworm moth,Prionoxystus robiniae (Peck). The four 3,5-geometrical isomers were synthesized and bioassayed in the laboratory and the field in 1972, 1973, and 1974. TheZ,E isomer was found to be active in the laboratory and a good attractant in the field. The synthesis of theZ,E isomer also produced considerable quantities of theE,E isomer, which is difficult to remove completely. TheE,E isomer does not inhibit the response of males to theZ,E isomer when it is present in amounts up to 20% of theZ,E isomer. The addition of a keeper, a volatility modifier, or an antioxidant prolonged the activity of the attractant for as much as 43 days. (Z,E)-3,5-Tetradecadien-1-ol acetate may be a natural pheromone, but it has not been chemically defined from female extract. There is EAG evidence that a second pheromonal component may be present. The attractant nevertheless provides a tool for population survey, behavioral studies, evaluation of economic impact, and possibly control.
    Type of Medium: Electronic Resource
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