The genomic rate and distribution of effects of deleterious mutations are i
mportant parameters in evolutionary theory. The most detailed information c
omes from the work of Mukai and Ohnishi, who allowed mutations to accumulat
e on Drosophila melanogaster second chromosomes, shielded from selection an
d recombination by being maintained heterozygous in males. Averaged over st
udies, the estimated rate of nonlethal viability mutations per second chrom
osome per generation under an equal-effects model, U-BM, was 0.12, suggesti
ng a high genomic mutation rate. We have performed a mutation-accumulation
experiment similar to those of Mukai and Ohnishi, except that three large h
omozygous control populations were maintained. Egg-to-adult viability of 72
nonlethal mutation-accumulation (MA) lines and the controls was assayed af
ter 27-33 generations of mutation accumulation. The rate of decline in mean
viability was significantly lower than observed by Mukai, and the rate of
increase in among-line variance was significantly higher, Our U-BM estimate
of 0.02 is much lower than the previous estimates. Our results suggest tha
t the rate of mutations that detectably reduce viability may not be much gr
eater than the lethal mutation rate (0.01 in these lines), but the results
also are consistent with models that include many mutations with very small
effects.