The role of developmental time in the world-wide dine of Adh and a Gpdh allele frequencies of Drosophila melanogaster, and the relationship with weight and some biochemical characters, were investigated. Experimental strains were constructed with different combinations of Adh and aGpdh alleles but with similar genetic background. Developmental time, adult weight, protein-and triglyceride-content, and ADH and aGPDH enzyme activity were measured at a rearing temperature of 20, 25 and 29°C. Genotype effects were found in all studied characters. In general the developmental times of genotypes were: Ad/IFF < Adh' a GpdhFS = aGpdhSS. Developmental time and adult weight were strongly affected by rearing temperature.Triglyceride content and ADFI and a GPDH enzyme activity were slightly affected by temperature. Interactions between genotype and temperature effects were found for developmental rate, adult weight and protein content. No trade off was observed between developmental time on the one hand and adult weight, protein-and triglyceride-content, and ADH and a GPDH enzyme activity on the other hand. It is argued that developmental rate differences might be one of the underlying mechanisms of the world-wide dine of the Adh and a GPdh allele frequencies.Keywords: Adh, a Gpdh, developmental time, Drosophila melanogaster, temperature, weight.
IntroductionThe alcohol dehydrogenase (Adh) and a-glycerophosphate dehydrogenase (a Gpdh) loci are two of the most extensively studied allozyme systems of Drosophila melanogaster. They provide an excellent opportunity to study interactions between physiological effects of gene-enzyme systems. Both loci have two common electrophoretic alleles: AdhF, Adhs, aGpdh' and aGpdhS. Nearly all natural populations are polymorphic for both loci. The frequencies of these alleles show world-wide clinal variation: the frequencies of Adhs and aGpdhF decrease with increasing latitude (Oakeshott et al., 1982). An important question is whether these dines are under the control of natural selection. Correlation analysis of climatic data revealed no consistent significant correlations (Anderson et a!., 1987). In the laboratory, stress from alcohol or temperature can cause differential selection of Adh and aGpdh alleles (e.g. Van Delden, 1982; Zera et a!., 1985). Under normal laboratory conditions equilibrium selection has been demonstrated for Adh (Bijisma-Meeles & Bijlsma, 1988) and aGpdh (Palabost-Charles, 1980). Selection at temperatures between 25 and 30°C may lead to an increase of the Adhs and aGpdh' alleles (Alahiotis, 1982;Van Delden, 1984). Vigue et al. (1982) and Oakeshott et al. (1985), however, found no effect of temperature on Adh or aGpdh allele frequencies. Van Delden (1984) and Van Delden & Kamping (1989) ascribe the advantage of the Adhs and aGpdhF alleles at a higher temperature, for the greater part, to linkage of both alleles with the inversion In(2L)t.Differences in developmental time between genotypes may be an important underlying mechanism of selection. D...