To determine whether a 50-Hz magnetic field will induce mutations, a sex-linked recessive lethal test of Drosophila rnekunoguster was performed. Adult flies were exposed at an rms flux density of 500 FT or 5 mT to the homogeneous field of a Helmholtz coil. The ambient field to which controls were ex
Multigeneration exposure test of Drosophila melanogaster to ELF magnetic fields
β Scribed by Takehiko Kikuchi; Masahiro Ogawa; Yoshihisa Otaka; Masako Furuta
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 104 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0197-8462
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β¦ Synopsis
Mutations, other than dominant lethals, were accumulated on wild type second chromosomes (/) of Drosophila melanogaster during exposure to 50 Hz sinusoidal alternating magnetic fields of 0.5 or 5 mT (rms) for 40 generations by the Curly/Plum(Cy/Pm) accumulation method. We maintained, for 40 generations under continuous exposure, each (/) chromosome as a heterozygote with (Cy) chromosome. Viability of the (/) chromosome was tested by sib-mating of (Cy//) male and (Cy//) female in a culture every 10th generation to obtain the homozygote. Viability indices, defined as twice the ratio of number of (///) flies to that of (Cy//) flies plus 1 in the progeny of the test mating, also were calculated, which equaled 1.00 at the starting point. For the control and 0.5 and 5 mT exposed groups, percent frequencies of recessive lethal lines, defined as a line with (///) flies less than 0.3% in the test mating, were, respectively, 1.9, 0.9, and 2.9% (10th), 9.0, 4.9, and 9.5% (20th), 30.3, 22.9, and 30.4% (30th), and 39.9, 32.4, and 43.3% (40th generation). For the control and 0.5 and 5 mT groups, average viability indices, excluding lethals and markedly deleterious, were, respectively, 0.778, 0.796, and 0.752 (20th), 0.704, 0.698, and 0.694 (30th), and 0.669, 0.678, and 0.595 (40th generation). Their decreasing rates were 0.0054, 0.0059, and 0.0078 per generation. No significant difference was detected among the exposure levels in either the recessive lethal mutation frequency or the viability index.
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