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1.
J Chem Ecol ; 15(3): 1057-65, 1989 Mar.
Article in English | MEDLINE | ID: mdl-24271906

ABSTRACT

l,5,7-Trioxaspiro[5.5]undecane, an analog of the major sex pheromone (olean) of the olive fruit fly, was synthesized via two different routes and tested for biological activity under laboratory and field conditions. In laboratory tests, its activity was comparable to that of olean, especially when a stabilizer or a high concentration was used. In field tests, its activity reached the level of olean only when a stabilizer and an open-type dispenser, which allows high rates of evaporation, were used. The residual activity of the analog dispensers did not exceed two weeks both under laboratory and field conditions compared to over four months for olean.

2.
J Chem Ecol ; 11(3): 397-405, 1985 Mar.
Article in English | MEDLINE | ID: mdl-24309970

ABSTRACT

Male olive fruit fly attraction to the four synthetic components of the female sex attractant pheromone was studied under laboratory and field conditions. In laboratory tests males responded to all four components tested separately. Component I, (1,7-dioxaspiro[5.5]undecane) was more attractive than any of the remaining three components alone, but a combination of all four was more attractive than component I alone. In field tests with polyethylene vials as pheromone dispensers, the complete mixture, although not statistically significant, was constantly more attractive to males than component I alone. A tendency of enhancement of attraction of component I by combining it with component II (α-pinene) or III (n-nonanal) was also observed. In field tests with rubber septa as pheromone dispensers only component I was attractive. Mixtures containing component I were also attractive but not more attractive than component I alone. Evaporation rate and ratio of components as they come out of the dispenser appear to be critical for male response.

3.
J Chem Ecol ; 7(2): 437-44, 1981 Mar.
Article in English | MEDLINE | ID: mdl-24420489

ABSTRACT

The sex attractant pheromone produced by femaleDacus oleae Gmelin is a mixture of four compounds, two of which are found in the rectal gland and the other two elsewhere in the insect body. The ratio of these compounds in the pheromone blend was measured. Biological activity of all four compounds and their combinations was studied in lab and field cage tests. The most abundant compound in the mixture (55.7%) shows the highest biological activity. Recombination of all compounds significantly increases activity of the main compound.

4.
J Econ Entomol ; 66(1): 55-61, 1973 Feb.
Article in English | MEDLINE | ID: mdl-4690297
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