1971
DOI: 10.1017/s0016672300012453
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An estimate of heterosis inDrosophila melanogaster

Abstract: Twenty-five population cages of D. melanogaster were set up, each containing a different wild-type second chromosome and the marker chromosome Cy. In all but one case where contamination apparently occurred, the Cy chromosome persisted in the population at high frequency, showing a selective advantage of Cyj + heterozygotes over wildtype homozygotes. Overall, the results indicate that homozygosity of the entire second chromosome causes a depression in fitness of the order of 85%.

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Cited by 95 publications
(72 citation statements)
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References 7 publications
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“…The rationale behind this experiment is outlined by Sved and Ayala (1970) and has been successfully applied by Bijlsma et al (1999). In short, balancer homozygotes are lethal and the wildtype homozygotes may also have a decreased fitness because of inbreeding depression.…”
Section: Balancer Chromosome Introgression Experimentsmentioning
confidence: 99%
“…The rationale behind this experiment is outlined by Sved and Ayala (1970) and has been successfully applied by Bijlsma et al (1999). In short, balancer homozygotes are lethal and the wildtype homozygotes may also have a decreased fitness because of inbreeding depression.…”
Section: Balancer Chromosome Introgression Experimentsmentioning
confidence: 99%
“…14). For example, in natural populations of Drosophila, approximately 30% of chromosomes carry a recessive lethal, and chromosomes that do not carry a recessive lethal suffer from at least 30% depression in homozygous fitness (15)(16)(17)(18)(19)(20)(21)(22)(23)(24). These data suggest that many, if not most, deleterious mutations are likely to be fully or partially recessive, and such mutations can have a moderate to strong fitness effect in the homozygote.…”
mentioning
confidence: 99%
“…+ heterozygote is detected in cages of low modifier background (averages of fertility estimates were 0.63 and 0.44 in cages L1 and L2, respectively). This is not an unusual result because there are many cases in the literature where fertility selection is an important component of total selection (Polivanov & Anderson, 1969;Sved & Ayala, 1970;Sved, 1971;Bundgaard & Christiansen, 1972;Anderson et al, 1979). On the other hand, our experimental design for fitness estimation splits total fitness into a component of preadult survival or egg-to-adult viability and into an adult fitness component or fertility.…”
Section: Discussionmentioning
confidence: 82%
“…For fitness estimation the zygotic frequency of Ba! + heterozygotes was corrected as this frequency is estimated at the adult stage rather than the egg stage (see Sved, 1971). The null hypothesis of no selective differences between Ba!+ and +/+ genotypes was tested by means of two different statistical approaches: an approximate significance test based on the x2 distribution (see Materials and methods) and the 95 per cent bootstrap confidence intervals (Efron & Tibshirani, 1986).…”
Section: Discussionmentioning
confidence: 99%