The effect of stressful and nonstressful rearing temperatures on phenotypic variation of four quantitative characters (thorax length, wing length, number of sternopleural chaetae, number of arista branches) and on developmental stability (fluctuating asymmetry) of the three latter characters was estimated in two Drosophila species: Drosophila melanogash and Drosophila buzzatii.In both species, a general trend for increasing of phenotypic variation and fluctuating asymmetry at stress temperatures was observed; in fluctuating asymmetry, this effect was more pronounced. An increase of phenotypic variation under stress was shown for all characters examined except sternopleural chaeta number in D. buzzatii. Comparison of species responses suggests that the increase of variation in D. melanogash was somewhat higher than in D. buzzatii.

A study of 16 natural populations of Drosophila melanogaster from Eastern Europe, the Caucasus and Central Asia has revealed a dine in wing length associated with geographical position of the populations. Wing length was shown to be positively correlated with temperature. The coefficient of variation in wing length was significantly different in town and orchard populations. The existence of a dine in wing length in the northern part of the species range and in the region where migration must be substantial suggests strong selection pressure acting in natural populations of D.melanogaster.

No abstract

The role of genes in the expression of aggression and masculinity traits in humans has been a focus of recent behavioral genetic studies. This is the first study on the variation in aggression, the digit ratio (the ratio between the second and the fourth digits, 2D:4D), the directional asymmetry in 2D:4D (D(R-L)) and polymorphisms of the AR, DRD4, and 5-HTTL genes in simple hunter-gatherers, namely the Hadza of Tanzania (142 adult men). The distribution of AR, DRD4E3, and 5-HTTLPR genotypes and allele frequencies in Hadza was compared to other African populations on which the data were available. Hadza and Ariaal differed significantly in the distributions of frequencies of AR alleles with different numbers of CAG repeats. Hadza population was similar to other African populations in the distribution of allelic frequencies of the DRD4E3 locus, and to Afro-Americans in the distribution of allelic types of the 5-HTTLPR locus. We found no influence of AR gene on the right hand 2D:4D ratio, D(R-L), and any of aggression subscales of the Buss-Perry Aggression Questionnaire (AQ). Although, a weak positive correlation between CAG repeats and the left hand 2D:4D was found. The multiple regression analysis with digit ratios, D(R-L) and aggression subscales of AQ as dependent variables and the three gene candidates (AR, DRD4E3, and 5-HTTLPR) as independent variables revealed the following: men with lower number of CAG repeats had significantly lower left hand 2D:4D ratio; men with higher numbers of 48-bp unit copies in exon 3 of a VNTR polymorphism in the DRD4 gene had significantly lower digit ratios on both hands; no effect of the 5-HTTLPR gene on either the digit ratio or aggressive behavior. These findings demonstrate the complexity of gene effects on digit ratios and aggression and call for simultaneous analysis of more candidate genes. It is noteworthy that these results were obtained for a human population that is still practicing foraging and has been subjected to a high selective pressure due to harsh environments and practically has no access to modern medical care. Hadza are highly egalitarian, and their culture does not favor persons with a dominant or aggressive behavior. It is still to be found to what extent the relationships observed in this study are similar to those in other human populations.

Using an isofemale line analysis, we analysed the consequences of extreme rearing temperatures for genetic variation in quantitative characters in Drosophila melanogaster. Three types of characters were used: life history (viability and developmental time), body size (thorax length and wing length) and meristic (number of sternopleural chaetae and number of arista branches). Phenotypic variation significantly increased under stress conditions in all morphological characters studied; for viability, it increased at the low stress temperature. Genetic variation, measured by the coefficient of intraclass correlation, was generally higher at both low and high stress temperatures for thorax length and sternopleural chaeta number. For wing length and viability, genetic variation was higher at the low extreme temperature. No consistent trend was found for genetic variation in arista branch number and developmental time. Our results agree with the hypothesis that genetic variation is increased in stressful environments. A possible mechanism underlying this phenomenon is briefly discussed.