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Prospects for using pyroproxyfen‐treated targets for tsetse control
Author(s) -
Langley P. A.,
Hargrove J. W.,
Mauchamp B.,
Royer C.,
Oouchi H.
Publication year - 1993
Publication title -
entomologia experimentalis et applicata
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.765
H-Index - 83
eISSN - 1570-7458
pISSN - 0013-8703
DOI - 10.1111/j.1570-7458.1993.tb00703.x
Subject(s) - pyriproxyfen , netting , offspring , toxicology , zoology , biology , chemistry , pesticide , ecology , pregnancy , political science , law , genetics
Abstract Using 14 C cholesterol as a marker a positive correlation was established between the amount of oil (a chlorinated n‐alkane containing 43–46% chlorine, ‘cereclor S45’) picked up by an adult tsetse fly exposed by tarsal contact to a treated surface and the duration of such exposure. Only a poor uptake was achieved from netting surfaces treated with less than 50% oil in acetone. Terylene netting treated with radioactive pyriproxyfen, [1‐methyl‐2‐(4‐phenoxyphenoxy)ethoxy] pyridine, dissolved in cereclor, was exposed in the field for a year. After 9 months 20 % of the original radioactivity remained and was shown to be 95% authentic pyriproxyfen. Brief tarsal contact (up to 5 seconds) with such netting, by adult females of Glossina morsitans morsitans Westwood, reduced the viability of their offspring to 28–43% of untreated control values. The effect was greatest in the reproductive cycle immediately following contact. Between 10 and 12 months after treatment of the fabric the radioactivity fell to only 7% of the original level but was associated mainly (>80%) with intact pyriproxyfen. Exposure of female flies to this netting resulted in a positive correlation between the duration of exposure and the extent of suppression of offspring viability, such that 2 min was sufficient to reduce offspring viability to zero for the life of the female. Traps or targets impregnated with conventional formulations of pyrethroids to kill tsetse would have lost all their activity by this time. Results are discussed in terms of the prospects for using pyriproxyfen‐treated targets to sterilize female tsetse directly and also indirectly through the contamination of males prior to mating through contact with such targets.