A fine structure deletion map of the metD region of the chromosome of Salmonella typhimurium responsible for a high-affinity methionine transport system has been constructed. Complementation tests involving the introduction of metD+DNA contained in a pUC8 vector into metD strains indicated the presence of four complementation groups in the metD region. This suggested that the methionine system belongs to the osmotic shock-sensitive class of transport system, and therefore should possess a periplasmic methionine-binding protein and several membrane proteins. But a deletion mutation covering all known metD point mutations did not affect the level of a methionine binding activity in osmotic shock fluids, suggesting either that the deletion did not extend into the gene encoding the binding protein, or that the binding activity is not associated with the metD system. Possible reasons for the failure to isolate mutations in the gene for the binding protein are discussed.

We estimated genetic and environmental variance components for developmental time and dry weight at eclosion in Drosophila melanogaster raised in ten different environments (all combinations of 22, 25 and 28°C and 0·5, 1 and 4% yeast concentration, and 0·25% yeast at 25°C). We used six homozygous lines derived from a natural population for complete diallel crosses in each environment. Additive genetic variances were consistently low for both traits (h2 around 10%). The additive genetic variance of developmental time was larger at lower yeast concentrations, but the heritability did not increase because other components were also larger. The additive genetic effects of the six parental lines changed ranks across environments, suggesting a mechanism for the maintenance of genetic variation in heterogenous environments.

The variance due to non-directional dominance was small in most environments. However, there was directional dominance in the form of inbreeding depression for both traits. It was pronounced at high yeast levels and temperatures but disappeared when yeast or temperature were decreased. This meant that the heterozygous flies were more sensitive to environmental differences than homozygous flies. Because dominance effects are not heritable, this suggests that the evolution of plasticity can be constrained when dominance effects are important as a mechanism for plasticity.

Using a series of Hfr and F prime deletion strains, the F transfer inhibition gene finP has been mapped between ori and traJ. Marker rescue experiments with the Hfr deletion strains further showed that traO, the site of action of the transfer inhibitor, is located immediately to the left of, or possibly within, traJ, and that the polar mutation tra-4 lies in traK.

An account is given of the habitat and ecology of a wrackbed population of Coelopa frigida (Fab.). The spatial distribution of the third-instar larvae was found to be patchy. This is due to a preference of adult flies for oviposition sites in zones of high temperature within the wrackbed. The relationship between larval density and temperature was found to account only in part for the patchy distribution, a second factor being the formation of family aggregates within each temperature zone. The effect of this type of spatial distribution on the interpretation of genetic sampling methods for the population is discussed.

Samples of third-instar larvae from the wrackbed population have been analysed for the presence of recessive embryonic lethals in three consecutive years from 1957 to 1959. From a total of 528 gametes tested, 44 recessive embryonic lethals were isolated. Cross tests for allelism showed that certain lethals were repeated within samples taken in the same year.

The gross frequency of embryonic lethals is shown to be independent of seasonal changes in population density. Estimates of gene frequency are made for certain individual lethals and these are shown to be greater than expected on the basis of the census size of the population. Possible causes of this discrepancy are examined.

1. The comparison of the dry weight of thin layer haploid and diploid colonies of A. niger on complete medium and complete medium supplemented with p-fluoro-phenylalanine led to the conclusion that there is a difference in growth rates of hyphae under these different conditions.

2. The growth curves of the same strains on both media were established. On complete medium, haploids and diploid show a growth rate increasing linearly for about 20 h after germination and reaching a maximum which is then maintained. On p-fluorophenylalanine, the haploids show a similar curve, although the maximum growth rate reached and maintained is about half that on complete medium; for the diploid, however, the maximum is less than the corresponding one in the haploid and, once this maximum has been reached, the growth rate goes down linearly to a very low value which is then maintained.

3. The cytological study of the hyphal tip cell showed, in the presence of the amino acid analogue, a reduction of the mean size of the diploid nuclei together with an increase of the number of nuclear fragments. This explains the growth rates observed and is accepted as a confirmation that p-fluorophenylalanine, by its action on the mitosis, favours chromosome losses which lead finally to the production of haploid nuclei.

The Uq transposable element is one of two transposable elements consistently found in maize (Zea mays L.) populations. Populations developed from two independent recurrent selection programs initiated in the Iowa Stiff Stalk Synthetic (BSSS) maize population were tested for the frequency of Uq transposable elements to determine how Uq frequency has changed with cycles of recurrent selection. In the first programme, 13 cycles of half-sib and S2 progeny recurrent selection [BSSS(S)C13] have been completed and 10 of the 13 cycles were assayed for active Uq elements. In the second programme, 11 cycles of reciprocal recurrent selection [BSSS(R)C11] have been completed and five of the 11 cycles were assayed for active Uq elements. The frequency of Uq was different for the two recurrent-selection programmes. The percentage of plants containing active Uq elements increased from 19% (BSSS) to 91% [BSSS(S)C13] at a linear rate after 13 cycles of half-sib and S2 progeny recurrent selection, whereas the percentage of plants containing active Uq elements decreased from 19% (BSSS) to 0% [BSSS(R)C11] after 11 cycles of reciprocal recurrent selection, with extinction of the Uq element occurring between the fifth and sixth cycles of selection. Our data suggest that the increase in frequency of Uq with half-sib and S2 progeny recurrent selection was predominantly due to random genetic drift coupled with a selective advantage possibly associated with a region of the genome linked to Uq. Neither replicative transposition or chromosome assortment and segregation can be invoked to explain the change in frequency of Uq in these populations. The extinction of Uq after reciprocal recurrent selection was best explained by random genetic drift.

A strain of mice that had ceased to respond to selection for high litter size was inbred with continued selection. Depression of the mean proved the existence of residual genetic variance. Four lines survived the inbreeding, and one reached 20 generations with a mean equal to the original strain, thus disproving overdominance as a major cause of the residual variation. The four selected inbred lines were crossed and a new strain derived from the cross was maintained in parallel with the original strain. The new strain showed an improvement of 1·5 mice per litter over the original strain. Thus selection with inbreeding was able to achieve an advance beyond the limit attained by the original selection.

The hypothesis that the residual variation was due to genes with simple dominance was tested by seeing if it could account for the observations with reasonable values of the relevant parameters. The improvement made by the inbreeding and crossing required the elimination of about 30 recessive genes with effects (homozygote difference) of 0·5 phenotypic standard deviations and gene frequencies of 0·2. Consideration of the mean levels of the selected inbred lines in conjunction with the rate of depression found on inbreeding without selection showed that the selection with inbreeding had eliminated about 75% of the segregating reces-sives. The number of genes contributing to the residual variance was therefore about 40. The additive variance generated by these genes was just consistent with the estimate of zero from the realized heritability. Consideration of the original selection showed that about half the genes could have been still segregating when the response ceased. The hypothesis therefore requires the number of genes in the base population to have been about 80. The number of genes required, though large, does not seem impossible, and the hypothesis of genes with simple dominance can account for all the observations.

The consequences of repeated backcrossing to a fixed parent are examined for haploid eukaryotes having a transitory diploid phase. The isogenicity attained in the absence of selected markers depends on the number of chromosomes and the total genetic map length, while the isogenicity of a chromosome carrying a selected marker increases more slowly and depends on the size of the chromosome. As inbreeding proceeds, the remaining non-isogenic material is not distributed evenly to all of the progeny. Instead, the majority of the progeny are completely isogenic with the fixed parent (with the exception of a region surrounding each selected marker), while the non-isogenic material is concentrated in a minority of the progeny. Even when the average isogenicity of the progeny and the fixed parent exceeds 99%, a significant proportion of the progeny will contain tracts of non-isogenic material which average several map units in length. Minor modifications enable these results to be applied to diploide. Examples show how to determine the degree of isogenicity produced by a given number of backcrosses in several specific situations.

Mice were selected for one of three criteria: appetite (A), measured as 4- to 6-week food intake, adjusted by phenotypic regression to minimize change in 4-week body weight, fat percentage (F), using the ratio of gonadal fat pad weight to body weight in 10-week-old males, and total lean mass (protein, P), using the index, body weight in 10-week-old males − (8 × gonadal fat pad weight). For each selection criterion, there were 3 high, 3 low and 3 unselected control lines. At generation 11, the high and low A lines diverged by 17% of the control mean and the realized heritability from within family selection of adjusted food intake was 15%. Selection for this character produced changes in body weight, gross efficiency from 4 to 6 weeks, and percentage of fat, the high lines being heavier, more efficient and less fat than the lows. The high and low F lines diverged by 80% of the control mean and the realized heritability of the ratio of gonadal fat pad weight to body weight was 44%. Selection for this character produced changes in total fat per cent, but little change in percentage protein, body weight, food intake or gross efficiency. The high and low P lines diverged by 40% of the control mean and realized heritability of the lean mass index (10-week weight − [8 × gonadal fat pad weight]) was 51%. Selection for an increase in the index increased body weight at all ages, food intake and 4- to 6-week gross efficiency. There was no change in percentage fat. Responses in the selected traits were not highly correlated, and the different lines provide an opportunity for investigating responses in physiology, metabolism and gene products.

The model of Lyon & Mason (1977) which defines three subregions of the t complex (T, tail-determining; A, abnormal transmission ratio; L, lethal) has been extended in an interpretation of male fertility data obtained from the combination of TOrl with different t haplotypes. The results demonstrate: (1) the T region of most t haplotypes (t12, t0, tw18 and tw2) possess gene(s) that interact with the L region to give quasisterility; (2) the T region of t6 lacks the allele(s) that result in quasisterility; and (3) the T region interacts with the A region to modify the transmission ratios of t haplotypes. The results were discussed in terms of an interacting genetic system controlling male fertility.

Currently favoured models postulate that gene conversion is due to the correction of mis-matches in heteroduplex DNA. If heteroduplex is formed reciprocally on both chromatids participating in recombination, the mis-matches due to a heterozygous site will be different on the two chromatids, and there will be four correction probabilities to be taken into account. It is shown that, given the frequencies of the five different kinds of aberrant ascus ratios, it is possible to calculate four alternative sets of values for the four correction probabilities and the total number of asci in which heteroduplex is formed. These four solutions reduce in effect to two when there are no other markers distinguishing the two chromatids. With the aid of flanking markers and the assumption that heteroduplex formation is chemically polarized, it is possible, in principle, to choose one best solution.

The method has been applied to the five one-point crosses in Sordaria fimicola from which most data are available. The data from four different mutants crossed to wild type are compatible with a restricted model in which the correction frequencies, from mutant to wild and from wild to mutant, are the same on both chromatids. In the case of the fifth mutant the data are not consistent with this restricted model, and indicate different correction frequencies in the two chromatids.

An experimental evaluation of Robertson's (1970) theory concerning optimum intensities of selection for selection of varying durations has been carried out using published results from a long term selection study in Drosophila. Agreement of predicted rankings of treatments with expectations was excellent for low values of t/T (generations/total number scored) but poor for larger values of t/T. This was due to the 20% selection intensity treatments responding worse than expected and the 40% treatments relatively better than expected. Several possible reasons for the discrepancies exist but the most likely explanation is considered to be the greater reduction in effective population size due to selection in treatments with more intense selection.

The flux through the de novo fatty acid synthesis pathway was estimated in lines of mice which differed substantially in fat content following 26 generations of selection at 10 weeks of age. Previous estimates of lipogenic enzyme activities had indicated an increase in the capacity for lipogenesis in the Fat compared to the Lean line. Therefore the in vivo flux in lipogenesis was measured in both liver and gonadal fat pad (GFP) tissues of males at 5 and 10 weeks of age, using the rat of incorporation of 3H from 3H2O and 14C from acetate and citra te into total lipids. AT both ages and in both tissues the Fat line had a higher flux, about 20% increase in the liver and up to three-fold increase (range 1·2- to 3·4-fold) in the GFP. We conclude that direct selection for fatness in mice has resulted in metabolic changes in the ratio of de novo fatty acid synthesis, and that the changes are largely detectable before 10 weeks, the age of selection.

Ontogenetic series of phenotypic, additive genetic, maternal and environmental correlation matrices are presented and interpreted in the light of recent models for the Ontogenetic origin and variation in correlation between traits. A total of 432 mice from 108 full-sib families raised in a cross-fostering design were used to estimate the various components of phenotypic correlation for five live-body traits at eight ages. The level of genetic and phenotypic correlation decreased with age, while levels of maternal and environmental correlation remained more or less constant. Genetic correlations probably decreased due to compensatory growth. Phenotypic correlations decreased primarily due to the relative decrease in importance of highly correlated maternal effects and consequent increase in poorly correlated environmental effects as portions of phenotypic variation. The effect of compensatory growth on genetic correlation was also responsible for a portion of the decline in phenotypic correlation. Phenotypic correlation patterns remained constant over the ages studied here. It also seems likely the genetic, maternal and environmental correlation patterns do not change with age for the characters analysed.

Three anonymous chromosome 17 DNA markers, D17Tu36, D17Tu43, and D17Le66B, differentiate between house mouse species and/or between t chromosomes. The D17Tu36 probe, which maps near the Fu locus and to the In(17)4 on t chromosomes, identifies at least 15 haplotypes, each haplotype characterized by a particular combination of DNA fragments obtained after digestion with the Taq I restriction endonuclease. Ten of these haplotypes occur in Mus domesticus, while the remaining five occur in M. musculus. In each of these two species, one haplotype is borne by t chromosomes while the other haplotypes are present on non-r chromosomes. The D17Tu43 probe, which maps near the D17Leh122 locus and to the In(17)3 on t chromosomes, also identifies at least 15 haplotypes in Taq I DNA digests, of which nine occur in M. domesticus and six in M. musculus. One of the nine M. domesticus haplotypes is borne by t chromosomes, the other haplotypes are borne by non-f chromosomes; two of the six M. musculus haplotypes are borne by t chromosomes and the remaining four by non-f chromosomes. Some of the D17Tu43 haplotypes are widely distributed in a given species, while others appear to be population-specific. Exceptions to species-specificity are found only in a few mice captured near the M. domesticus-M. musculus hybrid zone or in t chromosomes that appear to be of hybrid origin. The D17Leh66B probe, which maps to the In(17)2, distinguishes three haplotypes of M. domesticus-dznved t chromosomes and one haplotype of M. musculus-derivzd t chromosomes. Because of these characteristics, the three markers are well suited for the study of mouse population genetics in general and of t chromosome population genetics in particular. A preliminary survey of wild M. domesticus and M. musculus populations has not uncovered any evidence of widespread introgression of genes from one species to the other; possible minorintrogressions were found only in the vicinity of the hybrid zone. Typing of inbred strains has revealed the contribution of only M. domesticus DNA to the chromosome 17 of the laboratory mouse.

The effect of migration and recombination on the equilibrium structure of populations subject to a common symmetric selection regime in all habitats is studied. Attention is restricted to a class of symmetric polymorphic equilibria which have been studied in two-deme systems by Bazykin (1972) and Karlin & McGregor (1972) for one locus and by Christiansen & Feldman (1975) for two loci. With increased migration and recombination the heterozygosity increases unless it is already at the maximum level. Although the populaton system as a whole is always at linkage equilibrium, the magnitude of linkage disequilibrium in the individual demes may either increase or decrease with more migration and recombination. In general, the less the migration and the less the recombination between interacting loci, the greater the possibilities of polymorphic equilibria.