scholarly journals THE EFFECTS OF SELECTION FOR LARVAL BEHAVIOR ON ADULT LIFE-HISTORY FEATURES IN DROSOPHILA MELANOGASTER

Evolution ◽  
2001 ◽  
Vol 55 (12) ◽  
pp. 2493-2502 ◽  
Author(s):  
Patricia A. Foley ◽  
L. S. Luckinbill
Evolution ◽  
1995 ◽  
Vol 49 (3) ◽  
pp. 538-544 ◽  
Author(s):  
Linda Partridge ◽  
Brian Barrie ◽  
Nicholas H. Barton ◽  
Kevin Fowler ◽  
Vernon French

2019 ◽  
Vol 375 (1790) ◽  
pp. 20190178 ◽  
Author(s):  
Venkatesh Nagarajan-Radha ◽  
Ian Aitkenhead ◽  
David J. Clancy ◽  
Steven L. Chown ◽  
Damian K. Dowling

Evolutionary theory proposes that maternal inheritance of mitochondria will facilitate the accumulation of mitochondrial DNA (mtDNA) mutations that are harmful to males but benign or beneficial to females. Furthermore, mtDNA haplotypes sampled from across a given species distribution are expected to differ in the number and identity of these ‘male-harming’ mutations they accumulate. Consequently, it is predicted that the genetic variation which delineates distinct mtDNA haplotypes of a given species should confer larger phenotypic effects on males than females (reflecting mtDNA mutations that are male-harming, but female-benign), or sexually antagonistic effects (reflecting mutations that are male-harming, but female-benefitting). These predictions have received support from recent work examining mitochondrial haplotypic effects on adult life-history traits in Drosophila melanogaster . Here, we explore whether similar signatures of male-bias or sexual antagonism extend to a key physiological trait—metabolic rate. We measured the effects of mitochondrial haplotypes on the amount of carbon dioxide produced by individual flies, controlling for mass and activity, across 13 strains of D. melanogaster that differed only in their mtDNA haplotype. The effects of mtDNA haplotype on metabolic rate were larger in males than females. Furthermore, we observed a negative intersexual correlation across the haplotypes for metabolic rate. Finally, we uncovered a male-specific negative correlation, across haplotypes, between metabolic rate and longevity. These results are consistent with the hypothesis that maternal mitochondrial inheritance has led to the accumulation of a sex-specific genetic load within the mitochondrial genome, which affects metabolic rate and that may have consequences for the evolution of sex differences in life history. This article is part of the theme issue ‘Linking the mitochondrial genotype to phenotype: a complex endeavour’.


Genetics ◽  
1981 ◽  
Vol 97 (1) ◽  
pp. 173-186 ◽  
Author(s):  
Michael R Rose ◽  
Brian Charlesworth

ABSTRACT A sib analysis of adult life-history characters was performed on about twelve hundred females from a laboratory Drosophila melanogaster population that had been sampled from nature and cultured so as to preserve its genetic variability. The following results were found. There was no detectable trend with age in additive or dominance genetic variances for age-specific fecundity. Environmental variance for age-specific fecundity increased with age. The genetic variance for fecundity characters was primarily additive. The genetic variance for longevity was primarily dominance variance. There were negative genetic correlations between early fecundity and lifespan, as well as between mean egg-laying rate and longevity.


2001 ◽  
Vol 2001 (1) ◽  
Author(s):  
Leo S. Luckinbill ◽  
Robert Arking ◽  
Michael J. Clare ◽  
William C. Cirocco ◽  
Steven A. Buck

Although theories of the evolution of senescence differ in the mode of action by which genes are thought to control the aging process, they all view the rate of senescence as an adaptable feature of life history and therefore modifiable by natural selection. Tests of theory, however, have generally yielded mixed results. The life-span of Drosophila melanogaster increased strongly in populations selected for late reproduction in these experiments. Delayed senescence was accompanied by a reduced early fecundity, suggesting pleiotropic genetic control of the aging process. Reproduced by permission. Leo S. Luckinbill, Robert Arking, Michael J. Clare, William C. Cirocco, Steven A. Buck, Selection for Delayed Senescence in Drosophila melanogaster. Evolution 38 , 996-1003 (1984).


Evolution ◽  
1995 ◽  
Vol 49 (3) ◽  
pp. 538 ◽  
Author(s):  
Linda Partridge ◽  
Brian Barrie ◽  
Nicholas H. Barton ◽  
Kevin Fowler ◽  
Vernon French

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