The fractionation experiment: reducing heterogeneity to investigate age-specific mortality in Drosophila

Age-specific mortality rates decelerate at older ages in both genetically homogenous and heterogeneous populations of Drosophila. One explanation proposed for deceleration is population heterogeneity. This hypothesis suggests that a population consists of sub-populations that differ in mortality cha...

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Bibliographic Details
Published inMechanisms of ageing and development Vol. 105; no. 3; pp. 301 - 317
Main Authors Khazaeli, Aziz A., Pletcher, Scott D., Curtsinger, James W.
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 16.11.1998
Elsevier Science
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Summary:Age-specific mortality rates decelerate at older ages in both genetically homogenous and heterogeneous populations of Drosophila. One explanation proposed for deceleration is population heterogeneity. This hypothesis suggests that a population consists of sub-populations that differ in mortality characteristics and that the deceleration is the result of selective survival of stronger individuals. Here we describe an experiment that fractionates populations into several sub-populations without changing the physiological characteristics of the post-fractionated populations. Through a careful process of selection of Drosophila eggs, larvae, pupae and adults, we attempt to reduce as much as possible the degree of pre-adult, environmentally induced heterogeneity among individuals of a genetically identical cohort. We then ask whether such cohorts, when compared to non-fractionated populations, exhibit a lesser degree of mortality deceleration at advanced ages. From a total of 106 fractionated and control populations, consisting of 51 331 individuals, 101 populations (93% of the fractionated populations and 100% of the control populations) exhibit a significant amount of mortality deceleration late in life. These observations suggest that environmental heterogeneity accrued during larval development is not a major factor contributing to mortality deceleration at older ages.
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ISSN:0047-6374
1872-6216
DOI:10.1016/S0047-6374(98)00102-X