RESUMO
In wind-tunnel bioassays, dispensers loaded with 1 microg of the synthetic major component (3E,8Z, 11Z)-3,8,11-tetradecatrienyl acetate (TDTA) of the sex pheromone emitted by Tuta absoluta (Meyrick) females were found to be highly attractive to conspecific males. Field experiments were conducted to evaluate the efficacy of five trap designs. The best trap, baited with 100 microg of the synthetic sex pheromone caught on average 1,200 males per trap per night, while those baited with virgin females caught only 201 males. The male response to this pheromone is restricted to the same early-morning time window during which females exhibit calling behavior. The high biological activity of the synthetic pheromone suggests that it could be useful for pest monitoring and in mating disruption.
Assuntos
Acetatos/farmacologia , Álcoois Graxos/farmacologia , Mariposas/fisiologia , Atrativos Sexuais/farmacologia , Animais , Bioensaio , Feminino , Masculino , Controle de Pragas , Dinâmica Populacional , Comportamento Sexual Animal , OlfatoRESUMO
The blood of the Mexican bean beetle (Epilachna varivestis) contains a homotropane alkaloid, euphococcinine (1). The beetles 'reflex bleed' when disturbed, thereby deploying the alkaloid, which is provenly deterrent to spiders and ants. Newly emerged adults lack the alkaloid, but the compound builds up to deterrent levels in their blood within days. Eggs and larvae of Epilachna are devoid of the compound.
Assuntos
Alcaloides/sangue , Besouros/metabolismo , Alcaloides/farmacologia , Animais , Comportamento Animal , Feminino , Masculino , Comportamento Predatório/efeitos dos fármacosRESUMO
Two compounds recently isolated from the defensive gland ofNecrodes surinamensis, α-and ß-necrodol, first representatives of a new category of monoterpenes (the necrodanes), are shown to be repellent to ants and other insects and irritating to cockroaches and flies. The compounds doubtless play a defensive role inNecrodes. The possible long-range applied significance of research on insect repellents is discussed.
RESUMO
Two straight-chain C(15) fish antifeedants have been isolated from the sea hare Aplysia brasiliana. Chemical, spectral, and x-ray diffraction studies led to the characterization of these medium-ring ethers as brasilenyne (2) and cis-dihydrorhodophytin (3). The oxonin ring system of 2 is novel in nature. Biosynthetic considerations permit the postulation that a third compound, a noncrystalline congener of these compounds, is cis-isodihydrohodophytin (4).