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  • 1
    ISSN: 1573-1561
    Keywords: Hymenoptera ; Alloxystidae ; hyperparasitoids ; ants ; Formicidae ; interactions ; aggression ; chemical defense ; 6-methyl-5-hepten-2-one ; actinidin ; biological significance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Foraging females of the aphid hyperparasitoidAlloxysta brevis were attacked by honeydew-collecting workers of the antLasius niger at the first encounter. However, ants abandoned their attacks quickly, and foragingA. brevis remained unmolested for a subsequent time interval of approximately 5 min, which is long enough for the hyperparasitoid to oviposit successfully. Furthermore, freshly killed intactA. brevis were disregarded by ants, while decapitated specimens were readily removed. We present evidence thatA. brevis females release a mandibular gland secretion, which contains 6-methyl-5-hepten-2-one, actinidin, and unidentified iridoids, in response to an ant attack. This secretion functions both as a measure of self-defense if the female is seized by an ant worker and as a repellent, which prevents ant attacks during subsequent encounters. This is the first evidence for chemical defense in a hymenopterous parasitoid. It enablesA. brevis females to hyperparasitize ant-attended aphids that constitute a major proportion of their hosts and significantly reduces mortality by ectohyperparasitoids.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 98 (1965), S. 3578-3581 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Halogenierungsgeschwindigkeit o-hydroxy- und o-carboxy-substituierter Acetophenonderivate wird durch Mineralsäuren nicht beeinflußt, da die in wäßriger Lösung gebildeten Protonenchelate das Molekül vor dem Einfluß von Fremdsäuren schützen. Die für α-Ketosäuren typische Metallionen-Katalyse der Halogenierung wird bei den untersuchten Derivaten des Acetophenons nicht beobachtet.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 98 (1965), S. 1938-1948 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Geschwindigkeiten der säure- und basenkatalysierten Keto-Enol-Umlagerung von Aceton, Methyläthylketon, Brenztraubensäure, Methylbrenztrauben-säure, Dimethylbrenztraubensäure und Lävulinsäure in wäßr. Lösung wurden durch kolorimetrische Messung der Anfangsgeschwindigkeit der Jodanlagerung bestimmt. Es zeigt sich, daß α-Ketosäuren auch in wäßrigem Medium als Protonenchelate vorliegen, wobei die Wasserstoff-Brücke durch intramolekulare Säurekatalyse die Umwandlungsgeschwindigkeit der Säuren erhöht und das Molekül gleichzeitig vor dem Angriff von Fremdsäuren schützt. Komplexaktive Metall-lonen (Zn) beschleunigen die Umwandlungsgeschwindigkeit der α-Ketosäuren erheblich.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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