PETER MEDAWAR proposed that senescence arises from an age-related decl
ine in tile force of selection, which allows late-acting deleterious m
utations to accumulate. Subsequent workers have suggested that mutatio
n accumulation could produce an age-related increase in additive genet
ic variance (V-A) for fitness traits, as recently found in Drosophila
melanogaster. Here we report results from a genetic analysis of mortal
ity in 65,134 D. melanogaster. Additive genetic variance for female mo
rtality rates increases from 0.007 in the first week of life to 0.325
by the third week, and then declines to 0.002 by the seventh week. Mal
es show a similar pattern, though total variance is lower than in fema
les. In contrast to a predicted divergence in mortality curves, mortal
ity curves of different genotypes are roughly parallel. Using a three-
parameter model, we find significant V-A for the slope and constant te
rm of the curve describing age-specific mortality rates, and also for
the rate at which mortality decelerates late in life. These results fa
il to support a prediction derived from MEDAWAR'S ''mutation accumulat
ion'' theory for the evolution of senescence. However, our results cou
ld be consistent with alternative interpretations of evolutionary mode
ls of aging.